An Overview on Catalytic Hydrodeoxygenation of Pyrolysis Oil and Its Model Compounds

Pyrolysis is considered the most promising way to convert biomass to fuels. Upgrading biomass pyrolysis oil is essential to produce high quality hydrocarbon fuels. Upgrading technologies have been developed for decades, and this review focuses on the hydrodeoxygenation (HDO). In order to declare the need for upgrading, properties of pyrolysis oil are firstly analyzed, and potential analysis methods including some novel methods are proposed. The high oxygen content of bio-oil leads to its undesirable properties, such as chemical instability and a strong tendency to re-polymerize. Acidity, low heating value, high viscosity and water content are not conductive to making bio-oils useful as fuels. Therefore, fast pyrolysis oils should be refined before producing deoxygenated products. After the analysis of pyrolysis oil, the HDO process is reviewed in detail. The HDO of model compounds including phenolics monomers, dimers, furans, carboxylic acids and carbohydrates is summarized to obtain sufficient information in understanding HDO reaction networks and mechanisms. Meanwhile, investigations of model compounds also make sense for screening and designing HDO catalysts. Then, we review the HDO of actual pyrolysis oil with different methods including two-stage treatment, co-feeding solvents and in-situ hydrogenation. The relative merits of each method are also expounded. Finally, HDO catalysts are reviewed in order of time. After the summarization of petroleum derived sulfured catalysts and noble metal catalysts, transitional metal carbide, nitride and phosphide materials are summarized as the new trend for their low cost and high stability. After major progress is reviewed, main problems are summarized and possible solutions are raised.


Introduction
Rapid economic development remarkably increases the energy demand, especially in transportation fuels.Environmental concerns and uneven distribution of fossil fuel resources have aroused interest in developing renewable sources.Progress in technology of converting renewable sources into energy and fuels has become a research highlight.Biomass, as the only renewable organic carbon source feedstock, is a suitable renewable feedstock that can be converted into chemicals and transportation fuels [1,2].Fast pyrolysis is a promising way to convert solid biomass to liquid products Catalysts 2017, 7, 169; doi:10.3390/catal7060169www.mdpi.com/journal/catalystsdue to its high economic efficiency [3].Different lignocellulosic biomass resources, including energy crops, forest waste residues, herbaceous and woody biomass, were studied to produce bio-oil through fast pyrolysis.Bio-oil generally contains 50-65 wt % organic components, involving acids, aldehydes, ketones, furans, phenolics, guaiacols, syringols and sugars; 15-30 wt % moisture; and 20 wt % colloidal fraction [4].Oxygens contained in these compounds cause undesirable properties such as low energy density, instability, high viscosity and corrosion.Therefore, removing redundant oxygen atoms is required for bio-oil upgrading.In the past decades, oxygen removal attracted researchers' attention all over the world.Since the 1990s, enormous papers in biomass pyrolysis oil upgrading were published and many great review papers inspired researchers all over the world.Hydrotreating is an effective way to upgrade bio-oil, which removes oxygen through HDO, generally at 400-773 K and high H 2 partial pressure.Different catalysts were used in HDO to remove the oxygen atom in the molecules.In this paper, after a brief introduction about the properties of bio-oil, we mainly focus on the recent progress in catalytic HDO of bio-oil.With the rapid development of catalysts and upgrading technology, we hope this review can provide useful information and inspire ideas in producing high quality bio-oil.

Properties of Bio-Oil
The elemental compositions of bio-oil and petroleum derived fuel are quite different, and the basic data are shown in Table 1.Normally, there is 15-30 wt % water in bio-oil, derived from the moisture in the feedstock and dehydration process during the pyrolysis.The existence of water lowers the heating value and flame temperature of bio-oil.On the other hand, water reduces the viscosity and enhances the fluidity.Due to relatively high amounts of carboxylic acids mainly formed from hemicellulose pyrolysis, bio-oil generally shows acidity with pH value between 2 and 4, resulting in fatal problems in downstream utilization [5].As shown in Table 1, the oxygen content of bio-oil can reach as high as 50%.The presence of oxygen is the main difference between bio-oils and hydrocarbon fuels.Since the oxygen content is quite high, the heating value of bio-oil is much lower than that of conventional fuel (50%).Bio-oil has a heating value of about 20 MJ/kg using lignocellulosic biomass as feedstock, while that of fossil fuel is 45.5 MJ/kg.In addition, immiscibility with hydrocarbon fuels was also caused by the high oxygen content.As can be seen in Table 1, the viscosity of bio-oil is much higher than the conventional fuel.Depending on the types of biomass, pyrolysis conditions and storage time, a wide range of the bio-oil viscosities are obtained.Sipilaè et al. found that the viscosities of bio-oils were reduced with higher water content and less water insoluble components [5].Boucher et al. added methanol into bio-oil, finding that methanol reduced the density and viscosity and increased the stability.Moreover, the ash in bio-oil can cause problems in engines, such as corrosion, abrasion and deposition.Alkali and alkali earth metals are problematic components in the ash.The concentration of alkali and alkali earth metals in bio-oil are listed in Table 2.The concentrations are distinct when the bio-oils are produced from different feedstocks and conditions.The inorganic impurities in bio-oil could cause the catalyst poisoning during upgrading process.Yildiz et al. reported that an ash concentration of 3 wt % could have effect on the zeolite catalysts [9].Kubička and Horáček found that phosphorus, alkali and alkali earth metal could cause deactivation of CoMo/γ-Al 2 O 3 [10].Hot gas filtering is an efficient method to remove metallic heteroatoms in bio-oil.Scahill et al. employed hot gas filtration to decrease the alkali metal concentration below 10 ppm [11].The ash content of cassava stalk bio-oil decreased from 0.2% to 0.01% after using gas filter [12].Baldwin and Feik reduced the concentration of Ca < 10 ppm, Mg < 1 ppm, K < 5 ppm and Na < 5 ppm by hot gas filtration with a ceramic filter element [13].In order to understand where the ash come from and how it affect the bio-oil's properties, the existence form of alkali and alkaline metals in both biomass and pyrolysis vapor maybe more important.

Compositions of Bio-Oil
Insights in the composition of bio-oils are essential to determine its potential uses and the type of process required for upgrading methods [16].Wang et al. used gas chromatography-mass spectrometer (GC/MS) to analyze the composition of bio-oils and illustrate that most of the identified components were phenolic compounds attached with ketones or aldehydes groups [17].Therefore, bio-oils were highly hydrated, resulting in a difficult elimination of water.Conventional GC, especially when coupled with MS, is commonly used to analyze the chemical components for decades.However, GC-MS is not the most favorable technique for bio-oil characterization, as the poor elution properties of various compounds resulted in strong tail and coelution peaks.Comprehensive two-dimensional gas chromatography (GC × GC) coupled with different detectors is a new method in bio-oil characterization.Coelutions in the 1 DGC could be resolved by GC × GC, thus the number of compounds identified using GC × GC was approximately 4-7 times greater than that using conventional GC [18].However, only 25-40% of the analytes are detected because carbohydrates and lignin-derived oligomers are hard to evaporate which makes them difficult to enter the GC column [16].Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) is able to characterize the nonvolatile compounds in bio-oils [19].For pine pellets and peanut hull bio-oils characterized by FT-ICR MS, much lower oxygens per molecule was obtained in the oil phase than aqueous phase [20].Red pine bio-oil was analyzed by FT-ICR MS coupled with negative ion electrospray ionization (ESI) source.The predominant compounds in bio-oil are O2-O17 class species with 1-22 double-bond equivalent (DBE) values and 4-39 carbon numbers.The N 1 O x was also identified, which involved 1-16 DBE and 6-30 carbon numbers [21].NMR spectroscopy is also employed for the characterization of bio-oils, which can provide the concentrations of chemical functionalities and indications of highly substituted aromatic groups.For instance, the 13 C and DEPT analyses showed that corn stover bio-oil is highly branched owing to the high percentage of CH1 groups and the aromatic region generally has CH0:CH1 ratios of >2:1, suggesting that the average aromatic ring has at least four substituents.Additionally, high content of intact carbohydrate in corn stover bio-oil is demonstrated by 1H NMR analysis, because a relatively high concentration of protons was observed at ~5 ppm [22].Thus, integrated techniques are generally employed to obtain a comprehensive characterization of bio-oil.Currently, GC × GC combined with HRMS (using different ionization methods) seem to be most promising to obtain a specific chemical characterization of bio-oils.Spectroscopic method is also crucial as it enables to provide the bio-oils composition profile assessment [23].

HDO
As discussed earlier, some undesirable properties of bio-oil, such as chemical instability and a strong tendency to re-polymerize are caused by the high oxygen content.High viscosities, acidity, water content and low heating value are all major defects making it very hard to use bio-oils as fuels.Therefore, fast pyrolysis oils must be refined to produce deoxygenated products that are compatible with existing transportation fuels.
The general methods for bio-oil upgrading include physical, chemical and catalytic process.Physical upgrading includes filtration, solvent addition and emulsion.Liquid filtration is extremely difficult because of the physicochemical properties of bio-oil, while hot-vapor filtration can lower the average molecular weight of the liquid product and improve its stability during accelerated aging studies [13].For solvent addition and emulsion, solvents and surfactants are added into bio-oil to improve stability.Chemical upgrading mainly involves esterification, aqueous phase processing, mild cracking, gasification, etc. Catalytic upgrading pathways include HDO, zeolite cracking and steam reforming, of which the last one is a route to produce H 2 , not transportation fuel.Zeolite cracking is correlated with fluid catalytic cracking (FCC) of petroleum fractions, where oxygen atoms are removed by simultaneous dehydration-decarboxylation reactions over cracking catalysts (generally acidic zeolite) at atmospheric pressure without external H 2 .However, a major defect of this method is the low hydrocarbon yield due to severe carbonaceous deposits and dealumination of zeolite.Hydrotreating is also a conventional process for petroleum reforming, including hydrodesulfurization (HDS), hydrodenitrogenation (HDN), and HDO to remove sulfur, nitrogen, and oxygen heteroatoms respectively.Unlike petroleum oil, the content of sulfur and nitrogen in bio-oils is negligible whereas O content is extremely high.Hence, HDO becomes a crucial research topic.During HDO, reactions may occur including deoxygenation (C-O cleavage), hydrogenation (saturation of C=O and aromatic rings), hydrogenolysis, hydrocracking, etc.

HDO of Model Compounds
The reaction pathway of bio-oil HDO is still not clear due to its complicated nature resulting in numerous concurrent reactions during the upgrading process.Therefore, rather than employing pyrolysis oil at lab-scale, most studies use model compounds to obtain sufficient information in order to understand HDO reaction networks and mechanisms.Meanwhile, model compounds experiments contribute to screening and designing HDO catalysts [24].Currently, model compounds are selected among the most active compounds which will cause the instability of bio-oil.These compounds with different functional groups allow one to investigate the relative activities and selectivity of different reactions, such as dehydration, decarboxylation, hydrogenation, hydrogenolysis and hydrocracking.Furthermore, dimeric compounds were also selected as model compounds to provide an insight into the cleavage of some major types of linkage.

HDO of Aromatic Monomers
Since bio-oil contains almost 30 wt % of aromatic compound which has high energy density [25], a large amount of researches focus on HDO of these compounds.Additionally, the existence of phenolic compounds is considered as the primary cause for coke formation and catalyst deactivation [26].Thus, conversion of these oxygen-contained aromatic compounds is important in bio-oil upgrading.
Phenol is widely investigated as a model compound in HDO process because of its simple structure.In accordance with numerous investigations, HDO of phenol undergoes two main parallel routes.The first route is direct deoxygenation (DDO) that leads to formation of benzene by the cleavage of C-O bond.The second is hydrogenation (HYD), in which the aromatic ring is hydrogenated to cyclohexanol.Subsequent hydrogenation of benzene or deoxygenation of cyclohexanol occurs, leading to the formation of cyclohexane.Meanwhile, alkylation and etherification take place to form bicyclic compounds.Hong et al. also reported similar reaction pathways of phenol to bicyclics over Pt/HY catalyst [27].Studies on both aqueous-phase and vapor-phase HDO of phenol indicated that non-sulfide catalysts favor HYD route to saturate the aromatic ring.For example, no aromatic hydrocarbons were produced in HDO of phenol over Pd/C and H 3 PO 4 at 523 K [25].Therefore, HDO catalysts properties can significantly affect the reaction pathways.
Anisole with a methoxyl group is another model compound used for the study of bio-oil HDO. Figure 1 shows a general reaction scheme of anisole HDO studied by Sankaranarayanan et al. over supported Ni and Co catalyst, involving four reaction pathways: (1) demethylation of anisole to phenol and methane; (2) direct deoxygenation to benzene and methanol; (3) hydrogenation to methyl cyclohexyl ether; and (4) isomerization to methylphenol and dimethylphenol [28].These primary products can be further converted to cyclohexane, cyclohexanol, methylcyclopentane, etc. Pichaikaran et al. studied the vapor-phase HDO of anisole over supported Ni and Ru catalysts atatmospheric pressure [29].The major products obtained are phenol, benzene and toluene, indicating that the conversion of anisole mainly proceeds via hydrodeoxygenation, hydrogenolysis and methyl group transfer.hydrogenated to cyclohexanol.Subsequent hydrogenation of benzene or deoxygenation of cyclohexanol occurs, leading to the formation of cyclohexane.Meanwhile, alkylation and etherification take place to form bicyclic compounds.Hong et al. also reported similar reaction pathways of phenol to bicyclics over Pt/HY catalyst [27].Studies on both aqueous-phase and vapor-phase HDO of phenol indicated that non-sulfide catalysts favor HYD route to saturate the aromatic ring.For example, no aromatic hydrocarbons were produced in HDO of phenol over Pd/C and H3PO4 at 523 K [25].Therefore, HDO catalysts properties can significantly affect the reaction pathways.
Anisole with a methoxyl group is another model compound used for the study of bio-oil HDO. Figure 1 shows a general reaction scheme of anisole HDO studied by Sankaranarayanan et al. over supported Ni and Co catalyst, involving four reaction pathways: (1) demethylation of anisole to phenol and methane; (2) direct deoxygenation to benzene and methanol; (3) hydrogenation to methyl cyclohexyl ether; and (4) isomerization to methylphenol and dimethylphenol [28].These primary products can be further converted to cyclohexane, cyclohexanol, methylcyclopentane, etc. Pichaikaran et al. studied the vapor-phase HDO of anisole over supported Ni and Ru catalysts atatmospheric pressure [29].The major products obtained are phenol, benzene and toluene, indicating that the conversion of anisole mainly proceeds via hydrodeoxygenation, hydrogenolysis and methyl group transfer.Guaiacol with two kinds of C-O bond (hydroxyl group (-OH) and methoxy group (-OCH3)) appears to be an attractive compound for bio-oil HDO.The HDO scheme of guaiacol proposed by Nguyen et al. is shown in Figure 2, indicating that the reactions proceeded via demethylation, demethoxylation, hydrogenation and methyl transfer [30].The results of numerous researches for guaiacol HDO with different catalyst indicated that the catalyst composition plays a significant role during the reaction.Zhao et al. studied vapor phase HDO of guaiacol catalyzed by supported metal phosphide.The formation of anisole demonstrated that dehydroxylation occurs as a new reaction pathway of guaiacol HDO.Meanwhile, the hydrogenation reaction did not take place under this condition since no saturated products were detected [31].

HDO of Aromatic Dimers
The water insoluble fraction, often known as pyrolytic lignin (PL), can account for 25-30% of the bio-oil [32].The oligomeric PL portion is considered to be responsible for poor properties like viscosity and instability.Bayerbach et al. proposed several oligomeric structures of pyrolytic lignin that are based on combinations of phenolic dimers with different linkers [33].Therefore, oligomers, especially phenolic dimers, were selected as model compounds to investigate the cleavage of typical linkages (e.g., β-O-4, α-O-4, and β-5) during HDO process.Jongerius et al. studied HDO of Guaiacol with two kinds of C-O bond (hydroxyl group (-OH) and methoxy group (-OCH 3 )) appears to be an attractive compound for bio-oil HDO.The HDO scheme of guaiacol proposed by Nguyen et al. is shown in Figure 2, indicating that the reactions proceeded via demethylation, demethoxylation, hydrogenation and methyl transfer [30].The results of numerous researches for guaiacol HDO with different catalyst indicated that the catalyst composition plays a significant role during the reaction.Zhao et al. studied vapor phase HDO of guaiacol catalyzed by supported metal phosphide.The formation of anisole demonstrated that dehydroxylation occurs as a new reaction pathway of guaiacol HDO.Meanwhile, the hydrogenation reaction did not take place under this condition since no saturated products were detected [31].

HDO of Aromatic Dimers
The water insoluble fraction, often known as pyrolytic lignin (PL), can account for 25-30% of the bio-oil [32].The oligomeric PL portion is considered to be responsible for poor properties like viscosity and instability.Bayerbach et al. proposed several oligomeric structures of pyrolytic lignin that are based on combinations of phenolic dimers with different linkers [33].Therefore, oligomers, especially phenolic dimers, were selected as model compounds to investigate the cleavage of typical linkages (e.g., β-O-4, α-O-4, and β-5) during HDO process.Jongerius et al. studied HDO of phenolic dimers over a commercial sulfide CoMo/Al 2 O 3 catalyst at 573 K and 50 bar H 2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5 linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H 2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2 -biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5 dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].

Substrates Conversion (%) Selectivity (%)
Catalysts 2017, 7, 169 6 of 22 phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].[36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].[36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].[36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].[36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].[36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].[36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].phenolic dimers over a commercial sulfide CoMo/Al2O3 catalyst at 573 K and 50 bar H2 pressure, revealing that ether linkages including β-O-4 and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage [34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table 3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol [35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products [36].The β-O-4 linkage was effectively cleaved to aromatic fragments, and its alcohol oxygen on alkyl chains was subsequently removed with loss of aromatic groups.Strassberger et al. obtained phenol and ethylbenzene as main products in HDO of 2-phenoxy-1-phenylethanone and its alcohol analog on supported copper catalysts.The mechanism for HDO of alcohol dimer was proposed as the hydrogenolysis of C-O (aryl) bond occurred to phenol and 1-phenylethanol, followed by hydrodeoxygenation to ethylbenzene.The alcohol dimers were also catalyzed by alumina to form oligomers as by-products [37].

HDO of Other Oxygenates
In addition to lignin-based aromatic oxygenates, furans, carboxylic acids, alcohols and carbohydrates are also common products in biomass pyrolysis.A number of investigations focused on HDO of these cellulosic or hemicellulosic fractions of biomass pyrolysis.
A hypothetical mechanism for furan HDO was proposed including two reaction routes.For one route, furan first formed a transition state, followed by the formation of butadiene which could further undergo hydrogenation to butane.Moreover, partial hydrogenation of the ring also occurred followed by ring opening to a new transition state, which subsequently decomposed to propylene or butylene [38].Zheng et al. proposed a proper pathway for vapor-phase HDO of furfural over Cu-based catalyst, as shown in Figure 3 [39].The conversion of furfural yields both furfuryl alcohol and furan via hydrogenation and C-C bond cleavage, followed by sequential hydrogenation to tetrahydrofurfuryl alcohol and tetrahydrofuran.In addition to tetrahydrofuran, n-butanol, n-butanal, ethanol and hydrocarbon also derive from furan conversion.Furthermore, 2-methyltetrahydrofuran, 2-pentanone, 2-pentanol and 1-pentanol are all the hydrogenation products of 2-methylfuran obtained from a cleavage of C-O bond.Sitthisa et al. carried out furfural HDO over supported metal catalysts under atmospheric pressure, indicating that the product distribution was strongly depended on the metal used in the catalyst.Butanal, butanol and butane were obtained by ring opening reaction on Ni/SiO2 catalyst, while Pd/SiO2 catalyzed the formation of furan by decarbonylation [40].

HDO of Other Oxygenates
In addition to lignin-based aromatic oxygenates, furans, carboxylic acids, alcohols and carbohydrates are also common products in biomass pyrolysis.A number of investigations focused on HDO of these cellulosic or hemicellulosic fractions of biomass pyrolysis.
A hypothetical mechanism for furan HDO was proposed including two reaction routes.For one route, furan first formed a transition state, followed by the formation of butadiene which could further undergo hydrogenation to butane.Moreover, partial hydrogenation of the ring also occurred followed by ring opening to a new transition state, which subsequently decomposed to propylene or butylene [38].Zheng et al. proposed a proper pathway for vapor-phase HDO of furfural over Cu-based catalyst, as shown in Figure 3 [39].The conversion of furfural yields both furfuryl alcohol and furan via hydrogenation and C-C bond cleavage, followed by sequential hydrogenation to tetrahydrofurfuryl alcohol and tetrahydrofuran.In addition to tetrahydrofuran, n-butanol, n-butanal, ethanol and hydrocarbon also derive from furan conversion.Furthermore, 2-methyltetrahydrofuran, 2-pentanone, 2-pentanol and 1-pentanol are all the hydrogenation products of 2-methylfuran obtained from a cleavage of C-O bond.Sitthisa et al. carried out furfural HDO over supported metal catalysts under atmospheric pressure, indicating that the product distribution was strongly depended on the metal used in the catalyst.Butanal, butanol and butane were obtained by ring opening reaction on Ni/SiO 2 catalyst, while Pd/SiO 2 catalyzed the formation of furan by decarbonylation [40].

HDO of Other Oxygenates
In addition to lignin-based aromatic oxygenates, furans, carboxylic acids, alcohols and carbohydrates are also common products in biomass pyrolysis.A number of investigations focused on HDO of these cellulosic or hemicellulosic fractions of biomass pyrolysis.
A hypothetical mechanism for furan HDO was proposed including two reaction routes.For one route, furan first formed a transition state, followed by the formation of butadiene which could further undergo hydrogenation to butane.Moreover, partial hydrogenation of the ring also occurred followed by ring opening to a new transition state, which subsequently decomposed to propylene or butylene [38].Zheng et al. proposed a proper pathway for vapor-phase HDO of furfural over Cu-based catalyst, as shown in Figure 3 [39].The conversion of furfural yields both furfuryl alcohol and furan via hydrogenation and C-C bond cleavage, followed by sequential hydrogenation to tetrahydrofurfuryl alcohol and tetrahydrofuran.In addition to tetrahydrofuran, n-butanol, n-butanal, ethanol and hydrocarbon also derive from furan conversion.Furthermore, 2-methyltetrahydrofuran, 2-pentanone, 2-pentanol and 1-pentanol are all the hydrogenation products of 2-methylfuran obtained from a cleavage of C-O bond.Sitthisa et al. carried out furfural HDO over supported metal catalysts under atmospheric pressure, indicating that the product distribution was strongly depended on the metal used in the catalyst.Butanal, butanol and butane were obtained by ring opening reaction on Ni/SiO2 catalyst, while Pd/SiO2 catalyzed the formation of furan by decarbonylation [40].Conversion of carboxylic acids is crucial since they are considered as typical component that contribute to the corrosive property of bio-oil.Figure 4 shows the reaction network of aqueous phase hydrogenation of acetic acid proposed by Wan and co-workers [41].Primary reaction of acetic acid includes dehydrogenation to acetate species or dehydroxylation to acetyl species.Acetate reacts further via decarboxylation or reforming to form CH 4 or H 2 , respectively.Acetyls can either decompose via the cleavage of C-C bond to CH 4 and CO or be converted to ethanol.The formed ethanol is further converted to ethane via hydrodeoxygenation, CH 4 via C-C bond cleavage, and ethyl acetate via esterification.Moreover, HDO of acetic acid mixed with p-cresol was studied on Ru/C catalyst at 573 K and 48 bar hydrogen pressure.In the mixed feed system, acetic acid hydrogenation was suppressed due to the competitive adsorption on catalyst surface.On the contrary, the HDO of p-cresol is promoted, resulting in high selectivity to methyl-cyclohexane.
Conversion of carboxylic acids is crucial since they are considered as typical component that contribute to the corrosive property of bio-oil.Figure 4 shows the reaction network of aqueous phase hydrogenation of acetic acid proposed by Wan and co-workers [41].Primary reaction of acetic acid includes dehydrogenation to acetate species or dehydroxylation to acetyl species.Acetate reacts further via decarboxylation or reforming to form CH4 or H2, respectively.Acetyls can either decompose via the cleavage of C-C bond to CH4 and CO or be converted to ethanol.The formed ethanol is further converted to ethane via hydrodeoxygenation, CH4 via C-C bond cleavage, and ethyl acetate via esterification.Moreover, HDO of acetic acid mixed with p-cresol was studied on Ru/C catalyst at 573 K and 48 bar hydrogen pressure.In the mixed feed system, acetic acid hydrogenation was suppressed due to the competitive adsorption on catalyst surface.On the contrary, the HDO of p-cresol is promoted, resulting in high selectivity to methyl-cyclohexane.Wildschut et al. selected D-glucose and D-cellobiose as model compounds for carbohydrates in bio-oil, and investigated the HDO of these monomeric sugars over Ru/C catalyst at 523 K and 100 bar H2 pressure.The main reaction pathway was D-sorbitol hydrogenation, followed by hydrogenolysis of smaller polyols (e.g., glycerol and propanediol) and gaseous hydrocarbon (e.g., methane and ethane).In addition to hydrogenation, a thermal pathway proceeded to form hydromethylfurfural, levulinic acid and humins.Furthermore, the study demonstrated that the acetic acid added in this system increased solids formation by promoting the thermal route [42].

HDO of Actual Pyrolysis Oil
Nemours studies focused on bio-oil hydrotreating to achieve liquid fuels compatible with petroleum fraction.Elliot et al. initially carried out HDO of poplar wood bio-oil over a sulfide CoMo catalyst in 1983.This direct hydrodeoxygenation yielded only 23 wt % upgraded oil and resulted in severe coke deposition and bed plugging [43].Xiong et al. also tested direct HDO of bio-oil using a Raney Ni catalyst in a batch reactor, leading to low yield of organic liquid [44].Therefore, in order to overcome the obstacles mentioned above, alternatives such as employing a two-stage process and co-feeding with solvents were investigated for bio-oil hydrotreatment.

Two-Stage Hydrotreatment
The two-stage process was initially carried out by researchers from Pacific Northwest National Laboratory (PNNL) in 1989 [45].The first stage was operated below 553 K over Ni or sulfide CoMo catalyst to produce stabilized oil by hydrotreating the most reactive compound such as furans aldehydes, and ketones.The second step was performed at severe conditions in a second stage using conventional petroleum hydrotreating catalyst.With the two-stage hydrotreatment, the yield of upgraded oil could be increased to 30-55% with the comparison of direct HDO, and the deoxygenation degrees could be up to 99% [46].Noble metal catalysts have also been applied to two-stage hydrotreatment by Elliot et al.It was demonstrated that Pd/C was an effective catalyst to Wildschut et al. selected D-glucose and D-cellobiose as model compounds for carbohydrates in bio-oil, and investigated the HDO of these monomeric sugars over Ru/C catalyst at 523 K and 100 bar H 2 pressure.The main reaction pathway was D-sorbitol hydrogenation, followed by hydrogenolysis of smaller polyols (e.g., glycerol and propanediol) and gaseous hydrocarbon (e.g., methane and ethane).In addition to hydrogenation, a thermal pathway proceeded to form hydromethylfurfural, levulinic acid and humins.Furthermore, the study demonstrated that the acetic acid added in this system increased solids formation by promoting the thermal route [42].

HDO of Actual Pyrolysis Oil
Nemours studies focused on bio-oil hydrotreating to achieve liquid fuels compatible with petroleum fraction.Elliot et al. initially carried out HDO of poplar wood bio-oil over a sulfide CoMo catalyst in 1983.This direct hydrodeoxygenation yielded only 23 wt % upgraded oil and resulted in severe coke deposition and bed plugging [43].Xiong et al. also tested direct HDO of bio-oil using a Raney Ni catalyst in a batch reactor, leading to low yield of organic liquid [44].Therefore, in order to overcome the obstacles mentioned above, alternatives such as employing a two-stage process and co-feeding with solvents were investigated for bio-oil hydrotreatment.

Two-Stage Hydrotreatment
The two-stage process was initially carried out by researchers from Pacific Northwest National Laboratory (PNNL) in 1989 [45].The first stage was operated below 553 K over Ni or sulfide CoMo catalyst to produce stabilized oil by hydrotreating the most reactive compound such as furans aldehydes, and ketones.The second step was performed at severe conditions in a second stage using conventional petroleum hydrotreating catalyst.With the two-stage hydrotreatment, the yield of upgraded oil could be increased to 30-55% with the comparison of direct HDO, and the deoxygenation degrees could be up to 99% [46].Noble metal catalysts have also been applied to two-stage hydrotreatment by Elliot et al.It was demonstrated that Pd/C was an effective catalyst to hydrogenate various bio-oils to stabilized oils suitable for more severe hydrocracking step.In the first hydrotreating step, the gas yield improved while the oil yield decreased at higher temperature, and the product oxygen contents reached the minimum level at 613 K.The procedure could successfully run for 10 to 100 h depending on the operating conditions.Subsequent step were performed at about 673 K under 103 bar using a conventional sulfide catalyst, and the oxygen content of final products were all below 1%.In addition to the configuration mentioned above, a non-isothermal system incorporating the two steps was further explored at 523-683 K under 138 bar.It was indicated that the non-isothermal configuration could effectively minimize the carbon loss leading to the higher oil yield (50%) compared to the sequential one [47].Gholizadeh et al. investigated the hydrotreament of mallee wood bio-oil in a non-isothermal configuration using NiMo/γ-Al 2 O 3 as main catalyst.The authors observed that the reaction temperature had a role in coke formation and quality of upgraded oil.Although Pd/C catalyst laid in upstream had some effects on stabilizing bio-oil, it was ineffective in keeping off coke formation in long-term operation [48].In order to increase catalyst lifetimes, PNNL partnered with Battelle developed a new process for bio-oil hydrotreatment based on a two-stage system.A cleanup step and ion exchange were performed before the first stabilization step, obtained the cleaned up bio-oil of which the contents of metallic impurities were obviously decreased.For the first reaction zone, non-carbon supported catalysts were employed and catalyst regeneration processes were developed.Therefore, the Battelle-PNNL bio-oil upgrading process is stable for over 1000 h time on stream [49].

Co-Feeding Solvents
Hydrogen donor solvents were widely used in the hydrogenation of coal liquids to remove the heteroatoms and decrease molecular weight.In order to facilitate the transformation of active hydrogen and reduce coke formation during HDO process, hydrogen donor solvents, such as tetralin and decalin, were used for bio-oil upgrading.Churin et al. investigated the influence of the presence of tetralin on hydrotreating of bio-oil over NiMo catalyst, indicating that the hydrogen donor resulted in an additional reduction in the oxygen content of 15% [50].The oil phase of sawdust bio-oil was upgraded by Zhang et al. over sulfide Co-Mo-P, using tetralin and tar oil as solvent, respectively.The authors considered that tetralin transferred hydrogen from the gas phase with high activity to the radical fragments in oil phase, leading to higher liquid yield and less gas, char and water [51].Zhang et al. used decalin as hydrogen donor in the hydrotreatment of bio-oil and its model compounds over Ni/TiO 2 -ZrO 2 at 573 K. Higher reaction conversion was obtained when the initial H 2 pressure increased, because the solubility of H 2 in decalin was improved with the increased pressure [52].Employing hydrogen donor solvent in bio-oil HDO significantly reduce the operating pressures and lighten charring and coking phenomena.Moreover, alkanes have also been used during bio-oil HDO.Zhao et al. investigated the HDO of n-hexane-extracted bio-oil over Ni/HZSM-5 under mild reaction conditions.The obtained liquid products were almost hydrocarbons including C5-C9 alkanes, cycloalkanes, and aromatics molecules [53].However, the hydrocarbon solvents cannot completely blend with crude bio-oil due to their hydrophobicity, which hinders the HDO reaction to some extent.Hence, supercritical solvents were used for bio-oil hydrotreating.Xu et al. selected 1-butanol as solvent in the supercritical upgrading of bio-oil over a Ru/C catalyst, indicating that the features of upgraded bio-oil were significantly improved.The authors further illustrated that the solvent acted as both reaction medium and reactant during the reaction [54].Oh et al. studied the HDO of bio-oil over Pt/C catalyst in the presence of three supercritical solvents with different polarities.The polar protic solvent (ethanol) efficiently improved the degree of deoxygenation and typical bio-oil properties, such as acidity, viscosity, HHV and water content, and the polar aprotic solvent (acetone) resulted in the highest yield of heavy oil.The non-polar ether hardly affected the organics, but improved its thermal stability [55].

In-Situ Hydrogenation
Recently, in-situ hydrogenation as a novel method using liquid hydrogenation donors instead of hydrogen gas attracted lots of interesting.Acids and alcohols are common hydrogenation donors, which can generate hydrogen via aqueous-phase reforming.Xiong et al. conducted an in-situ hydrogenation of rice husk bio-oil in the presence of formic acid over various metal catalysts.During the upgrading process, formic acid decomposed to produce hydrogen while by-product CO 2 dissolved in solvents improving the rate of hydrogenation.High yield of liquid phase (>86%) and slight coke formation (<5%) were achieved with partial hydrogenation that alkenyl and aldehyde groups were almost completely reduced [44].Xu et al. used methanol as hydrogen donor instead of hydrogen gas in the hydrogenation of bio-oil at 493 K and 30 bar.Over Raney Ni catalyst, ketones and aldehydes were converted to alcohols via in-situ hydrogenation, while esterification took place transforming acids to esters [56].Furthermore, the authors carried out the upgrading process of bio-oil in different hydrogen donors (methanol, ethanol and formic acid) over Ni based catalysts to investigate the effect of hydrogen donors on the in-situ hydrogenation.The results showed that compositions of the upgraded bio-oils were different according to different hydrogen donors.When alcohols were used as hydrogen donors, the acetic acid in bio-oil could be converted to esters through esterification reaction.The phenol conversion was promoted in the presence of formic acid, along with restraining the conversion of acetic acid [57].Currently, in-situ hydrogenation is not common for bio-oil upgrading due to its relative low hydrogenation degree leading to the intermediate hydrogenation products instead of hydrocarbons.

Transition Metal Sulfide Catalysts
Conventional HDS catalysts for petroleum refining, using Mo as active component, Co or Ni as promoter, are first employed for the hydrogenation of pyrolysis oil.The HDO reactions catalyzed by metal sulfides are summarized in Table 4.These HDS catalysts need to be kept in sulfide form, so a sulfur source like H 2 S is commonly added during the reaction due to the negligible sulfur content of bio-oil.However, severe carbon deposition caused by sulfur leaching prohibits further application of petroleum hydrotreating catalysts.A number of suitable catalysts were investigated by researchers.Recently, Pawelec et al. contributed a review on the HDO of biomass derived liquids over transition metal sulfide catalysts [58].This section focuses on the use of sulfide catalysts in HDO process.In an early investigation, sulfide CoMo and NiMo supported on γ-A1 2 O 3 were employed for HDO of carbonyl, carboxyl and guaiacyl groups.It is found that NiMoS/γ-A1 2 O 3 showed higher decarboxylating activity compared to CoMoS/γ-A1 2 O 3 and increased the content of heavy products in HDO process of guaiacol [68].Massoth et al. carried out phenol HDO catalyzed by sulfide CoMoS/A1 2 O 3 at 573 K and 28.5 bar hydrogen pressure and obtained benzene, cyclohexene, cyclohexane and H 2 O as major products [69].The mechanism of guaiacol HDO promoted by sulfide CoMo and NiMo/A1 2 O 3 involved demethylation, demethoxylation and deoxygenation, followed by benzene ring saturation [70].Compared with sulfide catalyst supported on A1 2 O 3 , Nava et al. found that the activity of all the studied sulfide CoMo catalysts supported on mesoporous silicates were much higher.The selected mesoporous silicates included disordered mesoporous silica (DMS-1), hexagonal mesoporous silica (HMS) and cubic mesoporous silica (SBA-15, SBA-16).Among these four catalysts, CoMo/SBA-16 was considered as the most effective catalyst, indicating that the support morphology could strongly influence the catalytic response of catalysts [71].Bui et al. investigated the effect of cobalt on MoS 2 catalyst during the conversion of guaiacol.With addition of cobalt, the direct deoxygenation pathway involved in guaiacol conversion was obviously enhanced compared to the non-promoted MoS 2 , resulting in higher selectivity of aromatic hydrocarbons [62].Yoosuk et al. compared the HDO activities of MoS 2 , NiMoS 2 and NiS 2 using phenol as a model substrate.They observed that NiMoS 2 were more active than either of the other two catalysts and the maximum synergy was observed at a Ni/(Mo + Ni) molar ratio of 0.3 [60].Several unsupported MoS 2 with different morphology were used by Yang et al for HDO of phenolic compounds.They found that was favored over MoS 2 with a lower degree of stacking (MoS 2 derived from AHM) facilitated the C-OH bond hydrogenolysis, whereas MoS 2 with a higher degree of stacking (exfoliated MoS 2 ) facilitated aromatic ring hydrogenation [61].

Noble Metal Catalysts
Noble metal catalysts such as Pt, Pd, Rh and Ru have high catalytic activities for hydrotreating and can obviously improve the H/C ratio of pyrolysis oil.A large study showed that noble metal catalysts had high activities for HDO of pyrolysis oil.The effect of Pt on oxygen removal was better than NiMo and CoMo catalysts under the same conditions.However, high costs and difficult recovery limit the industrial application of noble metal catalysts.Recent studies about HDO catalyzed by noble metal catalysts are listed in Table 5.
For this series of zirconia-supported catalysts (Pd, Pt, Rh/ZrO 2 ) studied by Arditanti et al., Pd/ZrO 2 gave the highest activity and Rh/ZrO 2 results least carbon deposition [72].All these noble metal catalysts showed higher activities than conventional CoMo/Al 2 O 3 .Zanuttini et al. carried out cresol deoxygenation with Pt-Al 2 O 3 catalysts at atmospheric pressure, observing that methylcyclohexane was the major product at low temperature, while toluene achieved its highest yield at 573 K [73].The vapor-phase HDO of anisole over a bifunctional Pt/Hβ catalyst was conducted by Zhu et al. at 673 K and atmospheric pressure showed that the major products were benzene, toluene and xylene.They found that the acidic function catalyzed transalkylation, meanwhile the metal function promoted both demethylation and hydrodeoxygenation.Thus, compared with H-Beta and Pt/SiO 2 catalysts, less phenolic compounds and saturated hydrocarbons were obtained on the bifunctional catalyst [74].In addition, a similar result was carried out from the HDO of m-cresol over the bifunctional Pt/HBeta catalyst [75].Dwiatmoko et al. performed HDO of phenolic monomers over Ru catalysts supported on five different carbon materials.Among these catalysts, Ru supported on multi-walled carbon nanotubes (Ru/MWCNT) exhibited the highest HDO activity, owing to high surface area of Ru and high external surface area of the MWCNT [76].Lu et al. synthesized TiO 2 -modified Pd/SiO 2 catalyst (TixPd/SiO 2 ) for the conversion of guaiacol to investigate synergistic effect between Ti and Pd.They reported that addition of TiO 2 suppressed the sintering of Pd particles resulting in high conversion of guaiacol, and TixPd/SiO 2 showed deoxygenation activity while Pd/SiO 2 only exhibits hydrogenation activity [77].Echeandia et al. compared the catalytic activities of Pd catalysts supported on different support (zeolite HY, Al 2 O 3 and HY-Al 2 O 3 ) for the HDO of phenol.The activity of Pd/20%HY-Al was the largest, which could be attributed to H-spillover phenomenon and a large Pd dispersion [78].

Non-Noble Metal Catalysts
Recently, non-noble metal catalysts including base metals, metal oxides, phosphides, carbides and nitrides are widely used for upgrading of bio-oil.Due to the low price of biomass feedstock, using noble catalysts in upgrading process is uneconomical.Therefore, HDO catalyzed by non-noble metal catalysts has drawn mounting attention.The HDO reactions catalyzed by non-noble metals are summarized in Table 6.
Mortensen et al. screened in total 23 catalysts for phenol HDO at 548 K and 100 bar, observing that Ni had the best performance among tested non-noble metal catalysts [93].Compared with the high activity of oxide supported nickel catalysts, Ni/AC showed very low activity for phenol HDO, proving that hydrogenation occurred on the oxidic support while deoxygenation took place on the crystallites.Interestingly, reverse result was obtained by Dongil et al. for the conversion of guaiacol over Ni/CNT catalysts at 50 bar and 573 K in a batch reactor [94].The guaiacol conversion could up to 100% yielding cyclohexanol, cyclohexane and methoxycyclohexanol as major products.These results means the property of support may also dramatically affect the HDO performances.Shafaghat and co-workers investigated the HDO of a phenolic mixture catalyzed by Ni/HBeta, Fe/HBeta and NiFe/HBeta [95].They observed that hydrogenation was the dominant pathway in producing cycloalkanes over Ni/HBeta, while aromatic hydrocarbons were mostly produced though hydrogenolysis over Fe/HBeta.The phenolic compounds catalyzed by NiFe/HBeta could be converted to both cycloalkanes and aromatic hydrocarbons due to the synergistic effect between Ni and Fe.Olcese et al. compared the activity of Fe/SiO 2 and Co/Kieselguhr for the gas phase HDO of guaiacol at 623-723 K [96].They found that Fe/SiO 2 showed good selectivity to form aromatic hydrocarbons but did not exhibit activity for the hydrogenation of the aromatic ring.The n-electrons of the oxygen atoms are more basic than the π-electrons of C=C aromatic system, so the O atoms in hydroxyl or methoxyl groups were adsorpted on the weak acidic OH sites.Subsequently, C-O cleavage was catalyzed by the active H-species coming from the dissociation of hydrogen molecules on the iron particles.Metallic oxide also been investigated as catalyst for bio-oil upgrading.Selvaraj et al. considered HDO of guaiacol over MoO 3 -NiO/mesoporous silicates at atmospheric pressure, observing the following order of HDO activities: MoO 3 -NiO/MAS (mesoporous aluminosilicate) > MoO 3 -NiO/Ti-SBA-15 > MoO 3 -NiO/SBA-15 [97].However, naphthenic hydrocarbon was the major product over MoO 3 -NiO/MAS compared to other catalysts, where and aromatic hydrocarbon was the major product.The effect of support on the catalytic activity was also investigated by Loricera and co-workers.ZnNi/Ti (TiO 2 ), ZnNi/2Ti-Si (hybrid 2TiO 2 -SiO 2 ), ZnNi/S15 (SBA-15) and ZnNi/Ti-S15 (SBA-15 decorated with TiO 2 ) were used for the HDO of phenol [98].It was found that large BET surface area and acidity of supports were conducive to improving the catalytic efficiency.Ghampson et al. investigated ReO x supported on oxidized carbon nanofiber (ReO x -CNFox) to catalyze phenol HDO at 573 K, finding that phenol was completely converted at 10% ReO x loading [99].The coordinatively unsaturated Re 4+ , which acts as a Lewis acid, interacts with the oxygen lone pair on phenol.The C-1 of phenol accepts H + from surface hydroxyl groups resulting in an adsorbed phenoxide ion.After that, benzene was produced though C-O bond cleavage and the recovery of the oxygen vacancy were accomplished by the elimination of water.
Metal carbides have attracted great attention as hydroprocessing catalysts since tungsten carbide (WC) was proved to have Pt-like property [100].Frühberger and Chen also reported that surface modified by carbon converts the reactivity of Mo to that of Pt-group metals [101].In particular, the catalytic activity of metal carbides can approach or surpass that of Pt-group metals in reaction like hydrogenation and dehydrogenation [102].Lee et al. investigated the vapor-phase HDO of anisole catalyzed by Mo 2 C at 420-520 K under ambient pressure, in which benzene selectivity was up to 90% and cyclohexane selectivity was lower than 9% [103].Chen et al. further obtained high yields of benzene and toluene from HDO of phenolic mixtures over Mo 2 C catalyst at 533-553 K and atmospheric hydrogen pressure.It is demonstrated that Ar-OCH 3 in guaiacol was cleaved prior to the Ar-OH, and the low selectivity for saturated hydrocarbons (e.g., cyclohexane and methylcyclohexane) was due to in-situ modification of Mo 2 C surface by oxygenates [104].Recently, Lu et al. synthesized two ordered mesoporous metal carbides, Mo 2 C and W 2 C, to investigated the conversion of anisole in gas-phase at relatively low temperatures (423-443 K) [105].Mesoporous W 2 C catalyst showed a highest benzene selectivity reported to date (~96%) in anisole HDO, ascribed to the stronger oxygen affinity of tungsten and stronger W−O bond in comparison to the Mo−O bond.Metal nitrides have also drawn interest as candidate catalysts for hydrotreating bio-oil because of the coexistence of acidic and basic sites on nitrides caused by electronegativity differences between the metal and nitrogen atoms [106].Currently, few researchers work on metal nitrides catalysts for bio-oil upgrading.Ghampson et al. considered the effect of Mo 2 N on the conversion of guaiacol at 573 K and 50 bar hydrogen pressure in a batch reactor, finding that Mo 2 N was the most active compared to Mo 2 N 0.78 and other molybdenum compounds [107].Moreover, the addition of cobalt produced higher yields of deoxygenated products than Mo 2 N due to the presence of Co 3 Mo 3 N particles.HDO of guaiacol catalyzed by Mo 2 N catalysts supported on activated carbons with different textural and chemical properties was studied by Sepúlveda and co-workers [108].The Mo 2 N/Norit catalyst exhibited highest activity relative to Mo 2 N/Cudu and Mo 2 N/Pica, because the high mesoporosity of Norit carbon facilitated reactant diffusion to the internal surfaces.Mo 2 N/Norit also displayed higher phenol/catechol ratio than other catalysts.Metal carbides, nitrides and sulfides have similar preparation method.Generally, the starting materials of Mo-based catalysts are MoO 3 or its precursor (e.g., ammonium heptamolybdate).Mo 2 C, Mo 2 N, MoS 2 could be prepared with pretreatment in CH 4 /CO/C 3 H 8 , NH 3 and H 2 S flow, respectively [109][110][111].Saito and Anderson compared the activities of these three catalysts with different pretreatments, indicating that Mo 2 C and Mo 2 N had similar adsorbability of hydrogen, which was three times higher than that of MoS 2 [111].
Due to the ensemble and/or ligand effects of P, transition-metal phosphides exhibit high activity as hydrotreating catalysts and have drawn great attention for bio-oil upgrading [112].Bui et al. synthesized a series of metal phosphides supported on SiO 2 to investigate the catalytic activity on conversions of 2-methyltetrahydrofuran at 573 K and 1 bar.The HDO activities decreased in the sequence of Ni 2 P > WP > MoP > CoP > FeP and the selectivity toward HDO products followed the order of MoP > WP > Ni 2 P > FeP > CoP (phosphite method) and MoP ~WP > FeP > Ni 2 P > CoP (phosphate method) [113].An investigation of the anisole HDO catalyzed by Ni 2 P/SiO 2 , MoP/SiO 2 , and NiMoP/SiO 2 with different Ni/Mo ratios led to the conclusion that Ni 2 P exhibit superior activity to that of MoP and the coexistent Ni and Mo could facilitate the phosphides dispersion.Three major products, phenol, benzene and cyclohexane, were obtained via demethylation, hydrogenolysis, and hydrogenation, and both metal sites and PO-H groups were active for these reactions [112].

Catalyst Deactivation
Catalyst deactivation is an obvious problem in HDO, which means loss of catalyst activity as the reaction progress.Catalyst deactivation can be caused by coking, sintering, poisoning, and metal deposition.Catalysts properties are influenced with the degree of these phenomena.Especially, carbon deposition is known as the major cause of HDO catalysts deactivation.Polymerization and polycondensation are considered as main reactions leading to coke formation due to the obvious difference between the average molecular weight of coke and those present in the feeds.Therefore, the adsorbed reactants have a significant effect on the degree of carbon deposition.Unsaturated oxygenates in bio-oil, especially phenols and furans, are regarded as the predominant coke precursors since they can strongly interact with the catalytic surface [114].Moreover, it has been reported that double-oxygen compounds were much more prone to coke formation than single-oxygen compounds [115].The HDO of anisole and guaiacol conducted by González-Borja and Resasco also suggested that more severe catalyst deactivation was observed with guaiacol relative to anisole [88].In addition to reactant structures, catalyst properties such as acidity play an important role in coke formation.In the study for HDO of guaiacol over CoMoS catalysts, Bui et al. reported the conventional alumina support obviously induced the formation of heavier products resulting in catalyst deactivation, while supports with less acidity (ZrO 2 and TiO 2 ) formed less heavy by-products [116].Meanwhile, it is proposed that Lewis acid sites bind reactant species adsorb to catalyst surface, and Brønsted acid sites supply protons to form carbocations as coke precursors [114].Zanuttini et al. confirmed that Pt/SiO 2 had higher carbon deposition in the HDO of m-cresol compared to Pt/Al 2 O 3 due to the presence of Brønsted acid sites on silica supported catalyst, while alumina catalyst only had Lewis acid sites [117].Therefore, the contribution of the Lewis and Brønsted acidic sites to coke formation is still debatable.Operating conditions such as temperature, H 2 pressure and contact time are also relevant to coke formation during hydroprocessing.Low H 2 pressure and reaction temperature tend to promote coke formation reactions rather than hydrogenation reaction.Li et al. studied the effect of reaction temperature on coke formation, finding that increased temperature caused severe coke formation despite the improvement of HDO extent [118].a CNF means carbon nanofiber; b CNT means carbon nanotube; c tungsten precursor was silicotungstic acid (HSiW); d tungsten precursor was phosphotungstic acid (HPW).

Conclusions
Although the hydrogenation technology applied for pyrolysis oil has been developed for decades, some problems still exist that clog the development of this technology.(1) High cost and low hydrogen efficiency: HDO process can improve the pyrolysis oil quality, but it generally has low hydrogen utilization efficiency.Now, a better way to optimize the process is the combination of different hydrogen production to supply operations such as two-stage hydrodeoxygenation and in situ hydrogenation.The combination of these operations lowers the operation cost and produces more high value chemicals.(2) Complexity of operation process: In order to make the system work continuously, solid particles in pyrolysis oil have to be removed.Downstream treatment after hydrodeoxygenation is required to remove water to lower the water content in the meantime.Another vital operation unit is hydrogen regeneration unit, which can decrease the hydrogen consumption.Due to the process in whole system is complex, effectively simplify the operation system can dramatically lower the cost and make it easy to enlarge the system.(3) Proper catalyst and catalytic system: One of the key research subjects is to find out suitable catalysts.Noble metals are considered as a kind of efficient catalysts if its high cost is not taken into consideration.
These problems we summarized have hindered further development of biomass pyrolysis oil for a long time.However, with the development of modern analysis instruments and new generation technology, we believe there will be some breakthrough in this area.(1) Understanding the composition of biomass pyrolysis oil: Since biomass pyrolysis oil is a mixture of organic compounds, the properties of these components are complex, and molecular weight distribution is also very wide.FT-ICR, NMR and GC × GC have been proven as powerful analysis methods to identify different groups, of which conventional GC/MS can only provide limited information about these components.MS is the most common way to identify chemicals in biomass research.Considering the conditions of pyrolysis oil, a soft ionization mass spectrum is a better choice to identify mixtures.With the rapid development of new mass spectrum, it gives us a better understanding about both organic and inorganic components.
(2) Understanding pyrolysis chemistry: Compared to other solid feedstock, biomass pyrolysis is a more complex process since it contains many O atoms.Thus, it is a big challenge to understand its pyrolysis pathways.Researchers designed different experiments to study the pyrolysis chemistry.Generally speaking, biomass pyrolysis contains two stage reactions.Thus, understanding the two stage reactions and their interactions are extremely of great value for pyrolyzer design and downstream processes.
(3) Catalyst and catalytic process design: A high efficient catalyst and catalytic process is the core of pyrolysis oil upgrading.Transitional metal carbides were proved to act like noble metals, which may give us a series of low cost catalyst systems which can work at low hydrogen pressure.A good design of catalytic process should be based on both catalytic reactions and interaction between reactions.Since different pyrolysis compositions have dramatically different properties and transform pathway, synergy effect of different components should be considered during the designation.
In this review, we summarized recent progress in biomass pyrolysis oil upgrading to hydrocarbon fuels, mainly focusing on hydrodeoxygenation process.Although biomass pyrolysis oil upgrading research has been developing for decades, problems still exist as the bottleneck for further industrialization.Herein, we proposed our solutions: with the usage of modern analysis technology to understand the pyrolysis intermediates and product distribution, a more precise reaction network should be developed which is extremely useful to understand what will be converted.With the help of more precisely understanding on upstream composition, high activity and selectivity catalysts can be designed.In addition, source of coke formation and effect of alkaline salt are profitable to extend the life-span of catalyst.Based on selected catalyst, a better catalytic process will be designed for large scale industrialization.

Table 1 .
Comparison between biomass derived bio-oil and diesel.

Table 2 .
The concentration of alkali and alkali earth metals in bio-oil.

Table 3 .
[35]odeoxygenation of Phenolic Dimers over Ru/HZSM-5[35].Zhang et al.tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol[35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products

Table 3 .
[35]odeoxygenation of Phenolic Dimers over Ru/HZSM-5[35].Zhang et al.tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol[35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products

Table 3 .
[35]odeoxygenation of Phenolic Dimers over Ru/HZSM-5[35].Zhang et al.tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table3, conversions of all the model compounds almost achieved 100% and the overall selectivity to alkenes were above 96% except 2,2′-biphenol[35].The 4-O-5 and α-O-4 dimers were quantitatively converted to cyclohexane and C6-C10 alkanes, respectively.The formation of C8-C10 alkanes during HDO of α-O-4 dimers started with acid catalyzed transalkylation of C6-C7 products, followed by the isomerization of substituted cyclohexanes on Brønsted acid sites.Ethylcyclohexane, the main product for HDO of β-5 dimers, was obtained by hydrogenation of aromatic ring followed by dehydration and hydrogenation reactions.One reason for the relatively low hydrogenation rate of 5-5′ dimer might be caused by its intramolecular hydrogen bonds that could hinder the attack of the catalyst.Parsell et al. used Zn/Pd/C catalyst for HDO of guaiacylglycerol-b-guaiacyl ether under relatively mild condition, 423 K and 20.7 bar hydrogen pressure, got complete conversion and yielded two main aromatic products

Table 3 .
[34]odeoxygenation of Phenolic Dimers over Ru/HZSM-5[35].and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage[34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table

Table 3 .
[34]odeoxygenation of Phenolic Dimers over Ru/HZSM-5[35].and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage[34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table

Table 3 .
[34]odeoxygenation of Phenolic Dimers over Ru/HZSM-5[35].and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage[34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table

Table 3 .
[34]odeoxygenation of Phenolic Dimers over Ru/HZSM-5[35].and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage[34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table

Table 3 .
[34]odeoxygenation of Phenolic Dimers over Ru/HZSM-5[35].and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage[34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table

Table 3 .
[34]odeoxygenation of Phenolic Dimers over Ru/HZSM-5[35].and phenylcoumaran can be broken under this condition, but not the 5-5′ linkage[34].Zhang et al. tested HDO of a series of phenolic dimes with Ru/HZSM-5 at 473 K and 50 bar of H2 in a batch reactor.As shown in Table