Multiscale Porous Carbon Materials by In Situ Growth of Metal–Organic Framework in the Micro-Channel of Delignified Wood for High-Performance Water Purification

Porous carbon materials are suitable as highly efficient adsorbents for the treatment of organic pollutants in wastewater. In this study, we developed multiscale porous and heteroatom (O, N)-doped activated carbon aerogels (CAs) based on mesoporous zeolitic imidazolate framework-8 (ZIF-8) nanocrystals and wood using 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) oxidation, in situ synthesis, and carbonization/activation. The surface carboxyl groups in a TEMPO-oxidized wood (TW) can provide considerably large nucleation sites for ZIF-8. Consequently, ZIF-8, with excellent porosity, was successfully loaded into the TW via in situ growth to enhance the specific surface area and enable heteroatom doping. Thereafter, the ZIF-8-loaded TW was subjected to a direct carbonization/activation process, and the obtained activated CA, denoted as ZIF-8/TW-CA, exhibited a highly interconnected porous structure containing multiscale (micro, meso, and macro) pores. Additionally, the resultant ZIF-8/TW-CA exhibited a low density, high specific surface area, and excellent organic dye adsorption capacity of 56.0 mg cm−3, 785.8 m2 g−1, and 169.4 mg g−1, respectively. Given its sustainable, scalable, and low-cost wood platform, the proposed high-performance CA is expected to enable the substantial expansion of strategies for environmental protection, energy storage, and catalysis.


Introduction
With the rapid development of human society, the world has become faced with severe environmental pollution issues caused by hazardous organic chemicals, such as dyestuffs, oils, and organic solvents [1][2][3].Particularly, industrial waste affects biodiversity, ecosystems, and human health through soil and water contamination.Organic dye chemicals are widely used in essential industries, such as dye, plastic, textile, paper, pharmaceutical, and food [4-9], and although most toxic organic dyes are filtered from industrial waste using water purification technology, their leakage into water bodies, even at low concentrations, can lead to serious environmental problems and hazards to human health.Particularly, their non-biodegradability in water, thermal stability, and use in everyday life increase their harmful effects [10][11][12].Thus, wastewater treatment is essential to protect ecosystems and humans from harmful water pollutants.To prevent an increase in the environmental hazards caused by organic waste, various wastewater treatment approaches, such as coagulation, filtration, precipitation, adsorption, ion exchange, and advanced oxidation processes, have been employed for the removal of organic dyes from water systems [13][14][15][16][17][18][19][20].Among them, the most common technique is adsorption based on the use of adsorbents (e.g., zeolite, clay, and silica) with high specific surface areas [21][22][23][24][25][26].Adsorption is a relatively simple, effective, and economical technique (based on materials and operation cost and the minimal production of secondary pollutants).Thus, it is highly desirable to develop a high-performance absorbent for treating organic pollutants.
Carbon aerogels (CAs), which exhibit a large surface area, low density, and high porosity, have recently attracted considerable attention in environmental treatment, energy storage, catalysis, and sensors fields [27][28][29][30].Over the past decades, CAs have been fabricated using (1) nanocarbon units (carbon nanotubes, carbon nanofibers, and graphene nanosheets) and (2) polymerized organic gels derived from precursors [31][32][33][34][35].However, despite their intrinsic benefits, their high manufacturing cost and complex manufacturing processes, which hinder their large-scale commercial production, have limited their further application.Furthermore, most precursors used for the fabrication of CAs are considered to be carcinogenic to humans.To address these limitations, several recent studies have reported the high adsorption capability of biomass-derived CAs for organic pollutants [36][37][38][39].For example, Yamauchi et al. reported the large-scale synthesis of biomass polymer-derived CAs using a simple and sustainable method as a high-performance adsorbent [40].They demonstrated that biomass material is a suitable building block for CAs owing to its natural abundance, sustainability, and cost-effectiveness.Additionally, they demonstrated the enhanced surface area and mechanical properties of nanoparticle-embedded CAs, thereby expanding the applications of CAs.
Wood, one of the most abundant natural biomasses, exhibits a hierarchical structure with parallel hollow tubes comprising cellulose nanofibers and an amorphous matrix of lignin and hemicellulose [41][42][43].As a biomass material, wood exhibits multiscale porous structures ranging from the macro to nano levels [44].Macroscopic pores, such as cell lumen, resin channels, and pit apertures, as well as mesoporous pores, such as pores in the cell wall, can provide large specific surface areas and strong adsorption capacities.This hierarchically porous structure along with its natural abundance makes it an ideal template for the development of functional green nanocomposites [45].Metal-organic frameworks (MOFs) are crystalline compounds, containing three-dimensional (3D) networks of metal ions and organic linkers, with tunable porosity [46,47].Recently, MOFs have been extensively investigated for separation, storage, catalysis, and sensing applications, owing to their high specific surface area, large porosity (micropores/mesopores), and low density [48][49][50][51][52][53][54][55][56][57].However, despite the innovative utilization of MOFs, most MOFs are produced in the form of crystals and powders, which limit their use in real-world applications.Recently, several studies have demonstrated the successful synthesis of wood/MOF composite adsorbents by the in situ synthesis of MOFs within the aligned wood channels [36,37,58,59].For example, He et al. developed ZIF-67@wood aerogel via the in situ wet chemical deposition of ZIF-67 on the wood aerogel for the adsorptive purification of polluted wastewater [36].However, the lack of continuous nucleation sites in natural wood templates results in a low mass loading and poor uniformity of MOFs, which significantly affect the adsorption efficiency of these adsorbents.To the best of our knowledge, there is only one report (Zhou et al. described a foam-like TEMPO-oxidized wood/MOF aerogels for efficient CO 2 capture) describing the use of a TEMPO-oxidized wood template for the in situ growth of MOFs [60].
Herein, we describe the development of high-performance activated CAs with a hierarchical pore structure ranging from the micro to meso-and macroscale by harnessing the advantages of wood and MOFs.To the best of our knowledge, this is the first report on a wood/ZIF-8-derived CA for the efficient removal of organic pollutants.In this study, a 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-oxidized wood (TW) template with surface carboxyl groups was utilized as an important building block for the CAs.The surface carboxyl groups in the TW enabled the coordination of the cellulose network with multivalent metal ions, resulting in the efficient nucleation and in situ growth of MOFs within the wood template.Additionally, ZIF-8 with a high specific surface area and nitrogen content was synthesized in situ inside the TW, after which the wood was subjected to a freeze-drying process to obtain ZIF-8/TW-A.Subsequently, the ZIF-8/TW-A was subjected to a direct carbonization/activation process to obtain a highly interconnected multiscale porous and O, N-doped CA (denoted by ZIF-8/TW-CA), where wood with a hierarchical cellular structure served as a template, and ZIF-8 provided micro and mesoporous networks.The resultant ZIF-8/TW-CA exhibited a low density, high specific surface area, and outstanding adsorption capacities for organic pollutants.

Preparation of the TEMPO-Oxidized Wood
First, the balsa wood was cut into the desired size and immersed in 6% NaClO solution with vacuum impregnation for 24 h.After delignification, the delignified wood (DW) was washed with deionized water (DIW), and the lignin contents of the DW were measured using the Klason method.Briefly, the dry mass (0.3 g, M 0 ) was measured and treated with H 2 SO 4 (72%, 3 mL) for 1 h at 30 • C. Thereafter, the mixtures were transferred to a beaker, diluted to 4% by mass of H 2 SO 4 by adding 84 mL of DIW, and then boiled in an autoclave (121 • C, 1 h).After cooling, the mixtures were filtered using a glass filter membrane and washed with 250 mL of DIW water.The insoluble materials were dried and weighed (M d ), and the lignin content was calculated as follows: (M d /M 0 ) × 100%.For TEMPO oxidation, the DW was immersed in TEMPO/NaClO/ NaClO 2 (0.016 g/1.25 mL/1.13 g) dissolved in PBS solution (100 mL, 0.1 M, pH 7.4) at 60 • C for 48 h.After the TEMPO oxidation, the TWs were washed in an ethanol/DIW mixture (1:1, v/v) and stored in methanol.

Preparation of ZIF-8/TW-A
ZIF-8/TW-A was synthesized according to a previously reported procedure [61].First, the TW was immersed for 8 h with vacuum infiltration to achieve ion exchange between Zn and Na ions in Zn(NO 3 ) 2 •6H 2 O 6 solution, which was prepared by dissolving 2.4 g of Zn(NO 3 ) 2 •6H 2 O in 20 g of methanol and 3 g of DIW.Subsequently, the 2-Melm solution (13.2 g of 2-Melm in 20 g of methanol and 3 g of DIW) was poured into the aforementioned solution.After 24 h, the ZIF-8/TW was washed with methanol, and the solvent was exchanged with tert-butanol.Thereafter, the ZIF-8/TW was subjected to freeze-drying.

Preparation of ZIF-8/TW-CA
First, the ZIF-8/TW-A composites were carbonized at 250 • C for 1 h in a tube furnace to remove water from the sample.Thereafter, the temperature was increased to 850 • C for 3 h in an N 2 atmosphere at a heating rate of 5 • C/min.After carbonization, the samples were further heated to 350 • C for 1 h in air at a heating rate of 5 • C/min.For comparison, ZIF-8/DW-CA samples were prepared without TEMPO oxidation, using the same process as that used for ZIF-8/TW-CA.

Characterizations
The morphology of the ZIF-8/wood-based CA was investigated using field emission scanning electron microscopy (FE-SEM; Carl Zeiss, model AURIGA, Oberkochen, Germany), and elemental analysis was performed using energy-dispersive X-ray spectroscopy (EDS).The thickness of the samples was measured using a digital caliper (Mitutoyo Co., model 2109S-10, Kawasaki, Japan).The argon adsorption isotherms were analyzed using a Micromeritics ASAP 2010 micropore system and calculated using the Brunauer-Emmett-Teller (BET) and density functional theory (DFT) method.Fourier transform infrared (FT-IR) spectroscopy data were recorded from 4000 to 400 cm −1 using a Spectrum One System FT-IR spectrometer (Perkin-Elmer, Waltham, MA, USA).The chemical composition of the surface elements from 0 to 1200 eV was investigated using X-ray photoelectron spectroscopy (XPS; Thermo Electron model, K-Alpha, Waltham, MA, USA), and the crystallinity of the samples was analyzed using X-ray diffraction (XRD; Bruker, model D8 Advance, Billerica, USA) in the scanning range of 3−60 • .Raman spectra were recorded using a spectrometer (QE-PRO, Ocean Optics, Inc., OR, USA) equipped with a 785 nm (22 mW) laser.Thermogravimetric analysis (TGA) was performed using a Discovery TGA (TA Instruments, New Castle, USA) under nitrogen atmosphere at a heating rate of 10 • C min −1 .Ultraviolet-visible (UV-VIS) curves were obtained using a UV-VIS spectrophotometer (Shimadzu, model UV-3600 Plus, Nishinokyo, Japan).

Adsorption Studies
The adsorption properties of ZIF-8/TW-CA were investigated via batch adsorption experiments with RhB.All experiments were performed by immersing 10 mg of the adsorbent samples in 10 mL of each concentration (10-1000 mg L −1 , pH 7) of RhB under stirring using a shaker at 80 rpm for 24 h.Thereafter, 1 M HCl and 1 M NaOH were added to the dye solutions to adjust the pH.The concentration of the solution after adsorption was analyzed using a UV-VIS spectrophotometer by measuring the prominent wavelength at 553 cm −1 .The adsorption spectra and standard calibration curves of the different concentrations of the RhB solution are illustrated in Figure S4.To evaluate the recyclability of the CA, the adsorbed adsorbent was rinsed thrice in a solution mixture containing ethanol and DIW (1:1, v/v) to desorb RhB.After washing, the sample was immersed in 10 mg L −1 of RhB again.The adsorption capacity (q e ) for RhB and the removal efficiency (%) were calculated as follows: where q e (mg g −1 ) is the quantity of RhB adsorbed at equilibrium; C 0 (mg L −1 ) is the initial concentration of RhB; C e (mg L −1 ) is the residual concentration of RhB solution after adsorption; and V (L) and m (g) are the volume of the adsorbate and mass of the adsorbent, respectively.

Adsorption Models
To understand the nonlinear forms of the kinetic adsorption and isotherm models, four adsorption models were adopted (isotherm model, nonlinear Langmuir (3) and nonlinear Freundlich (4); kinetic model, nonlinear pseudo-first-order (5) and nonlinear pseudosecond-order ( 6)).The equations and parameters of the adsorption models were expressed as follows: [62] q e = q max K L C e /(1

Results
Figure 1a shows a schematic representation of the fabrication of ZIF-8/TW-CA through delignification, TEMPO oxidation, in situ ZIF-8 synthesis, and carbonization processes.First, pristine woods were pretreated via delignification to enhance the porosity and chemi-cal accessibility of the woods (Figure 1a(i)) [63].After the pretreatment, the yellowish color of the wood changed into white, indicating the delignification of the wood (Figure S1a,b).The successful delignification of the wood was evaluated using the Klason method and FT-IR (Figure S2).The results reveal a reduction of approximately 90% in the lignin content of the DW (2.42%) compared to that of pristine wood (21.5%) (Figure S2a).Furthermore, the decrease in the lignin-specific IR peaks at 1590, 1501, and 1452 cm −1 , which can be attributed to aromatic skeletal vibration, and that at 1230 cm −1 , corresponding to the guaiacyl ring with C-O stretching, confirmed the removal of lignin from the wood (Figure S2b).Additionally, the decrease in the intensity of the carbonyl group (C=O) at 1737 cm −1 indicated the removal of hemicellulose from the wood channel and middle lamella [64,65].After delignification, we conducted TEMPO-mediated oxidation to selectively convert C6 primary hydroxyl groups to carboxyl groups on the surface of cellulose microfibrils (Figures 1a(ii) and S1c) to provide nucleation sites for the subsequent in situ ZIF-8 synthesis (Figure 1b).Conductometric titration revealed that the carboxyl group content in the TW was 1.68 mmolg −1 .After complete washing, the TWs were immersed in a zinc nitrate solution.The cell walls of the wood efficiently adsorbed Zn 2+ via the electrostatic interactions between Zn 2+ and the carboxylic groups.After methanol washing, the Zn 2+ -loaded TWs were transferred into an organic ligand solution to achieve the nucleation and growth of ZIF-8 nanoparticles (Figure 1a(iii),b).Thereafter, the sample was freeze-dried to obtain ZIF-8/TW-A (Figure S1d), after which ZIF-8/TW-A was carbonized into ZIF-8/TW-CA under a N 2 atmosphere at 850 • C and further activated at 350 • C in air (Figures 1a(iv) and S1e).After carbonization, the air activation as a physical activation can effectively improve the surface area of the hierarchical porous structure and increase the number of oxygen-containing functional groups on the carbon surface in the ZIF-8/TW-CA [66].
The FE-SEM images (Figure 2a-c) indicate that the pristine wood and TW exhibited a typical natural wood structure with honeycomb-like cellular structures and vertical channels, confirming that pretreatments, such as delignification and TEMPO oxidation, did not result in the structural collapse of the wood.Additionally, mesopores (2-50 nm) and macropores (>50 nm) were observed at the aligned cellulose fibers in the cell wall of TW (Figure 2d,g), which may be attributed to the delignification and TEMPO oxidation.The extensive loss of lignin and its conversion into carboxyl groups during delignification and TEMPO oxidation enhanced the cell wall porosity and increased the specific surface area.The enhanced porosity and surface area will induce good chemical accessibility for the subsequent in situ ZIF-8 synthesis.Figure 2e,h demonstrate the good deposition of ZIF-8 on the entire surface of the cell walls inside the TW without large aggregation.After carbonization, ZIF-8/TW-A was converted into ZIF-8/TW-CA.Although the size of the ZIF-8-derived nanoporous carbon particles decreased because of the decomposition of organic ligands, the final ZIF-8/TW-CA adequately retained the original ZIF-8 shape (Figure 2f,i).The carbonization temperature is one of the critical parameters that determines the surface area and pore volume of the nanoporous carbon [67].Additionally, after carbonization, the ZIF-8-embedded wood composites were converted into interconnected, heteroatom-doped, and porous CA by harnessing the advantages of ZIF-8 and wood [40].
Heteroatom-doped carbon is well known to exhibit excellent adsorption capabilities [68].Compared to that of ZIF-8/TW-A, the volume of ZIF-8/TW-CA reduced by approximately 40%.Additionally, ZIF-8/TW-CA exhibited a low density of 56 mg cm −3 .The FT-IR results demonstrate the successful chemical transformation during the fabrication of ZIF-8/TW-CA (Figure 3a).A strong IR peak of C=O carbonyl groups was observed in the FT-IR spectrum of TW at 1603 cm −1 , confirming the TEMPO oxidation of pristine wood.Additionally, the representative IR peaks of neat ZIF-8 nanoparticles at 1584 cm −1 , which is assigned to the C=N stretching, and within 1350-1500 cm −1 , which is attributed to the ring stretching in imidazole, were observed in the FT-IR spectrum of ZIF-8/TW-A.The FE-SEM images (Figure 2a-c) indicate that the pristine wood and TW exhibited a typical natural wood structure with honeycomb-like cellular structures and vertical channels, confirming that pretreatments, such as delignification and TEMPO oxidation, did not result in the structural collapse of the wood.Additionally, mesopores (2-50 nm) and macropores (>50 nm) were observed at the aligned cellulose fibers in the cell wall of TW (Figure 2d,g), which may be attributed to the delignification and TEMPO oxidation.The extensive loss of lignin and its conversion into carboxyl groups during delignification and TEMPO oxidation enhanced the cell wall porosity and increased the specific surface area.The enhanced porosity and surface area will induce good chemical accessibility for the subsequent in situ ZIF-8 synthesis.Figure 2e,h demonstrate the good deposition of ZIF-8 on the entire surface of the cell walls inside the TW without large aggregation.After carbonization, ZIF-8/TW-A was converted into ZIF-8/TW-CA.Although the size of the ZIF-8-derived nanoporous carbon particles decreased because of the decomposition of organic ligands, the final ZIF-8/TW-CA adequately retained the original ZIF-8 shape (Figure 2f,i).The carbonization temperature is one of the critical parameters that determines the surface area and pore volume of the nanoporous carbon [67].Additionally, after carbonization, the ZIF-8-embedded wood composites were converted into interconnected, heteroatom-doped, and porous CA by harnessing the advantages of ZIF-8 and wood [40].This suggests the successful in situ growth of ZIF-8 in the TW.The XRD pattern further confirmed the embedding of ZIF-8 into the TW template (Figures 3b and S3), in which two broad diffraction peaks were observed at approximately 14.8 • -16.8 • and 22.5 • , indicating the presence of cellulose I crystals in the wood.In addition, two broad diffraction peaks assigned to cellulose were observed in the XRD pattern of ZIF-8/TW-A, along with diffraction peaks at 7.2, 12.7, 16.3, and 18.4 • , which can be attributed to the (110), ( 211), (310), and (222) crystal faces of ZIF-8, respectively (Figure S3a), demonstrating the successful growth of ZIF-8 crystals.These XRD patterns are consistent with the FT-IR results (Figure 3a).Further, two broad peaks were observed in the XRD pattern of ZIF-8/TW-CA at 25 and 43 • , which are characteristic peaks of the (101) and (002) planes of carbon, respectively (Figure S3b) [40,60,66].Next, we examined the chemical composition and environment of ZIF-8/TW-A and ZIF-8/TW-CA using XPS (Figure 3c).Compared to ZIF-8/TW-A (prior to carbonization), ZIF-8/TW-CA did not exhibit a Zn-related signal peak, suggesting the efficient removal of Zn content via carbonization.In addition, the XPS profiles revealed that ZIF-8/TW-CA comprised C, O, and N elements.Three peaks were observed in the high-resolution C 1s spectrum (Figure 3d) at 284.4, 285.4,and 287.2 eV, which can be attributed to the characteristic signals of C-C, C-O, and O-C=O bonds, respectively [66].Additionally, three peaks were observed in the XPS O 1s spectrum (Figure 3e) at 530.8, 532.6, and 534.5 eV, which can be attributed to O-C=O, C=O, and C-O bonds, respectively [69].Four peaks were observed in the N 1s spectrum (Figure 3f) at 398.3, 399.5, 400.5, and 403.2 eV, which can be attributed to pyridinic-N, pyrrolic-N, oxidized-N, and graphitic-N, respectively [40].The introduction of heteroatoms (e.g., N, O) into the CA increased its adsorption ability for organic pollutants [70].The XPS results of ZIF-8/TW-A and ZIF-8/TW-CA are with the EDS results (Figure 2j,k).Heteroatom-doped carbon is well known to exhibit excellent adsorption capabilities [68].Compared to that of ZIF-8/TW-A, the volume of ZIF-8/TW-CA reduced by approximately 40%.Additionally, ZIF-8/TW-CA exhibited a low density of 56 mg cm −3 .The FT-IR results demonstrate the successful chemical transformation during the fabrication of ZIF-8/TW-CA (Figure 3a).A strong IR peak of C=O carbonyl groups was observed in the FT-IR spectrum of TW at 1603 cm −1 , confirming the TEMPO oxidation of pristine wood.Additionally, the representative IR peaks of neat ZIF-8 nanoparticles at 1584 cm −1 , which is assigned to the C=N stretching, and within 1350-1500 cm −1 , which is attributed to the ring stretching in imidazole, were observed in the FT-IR spectrum of ZIF-8/TW-A.The Raman spectra (Figure 4a) of ZIF-8/DW-CA and ZIF/TW-CA exhibited two characteristic carbon peaks at 1327 (D: disordered carbon) and 1588 (G: graphitic carbon).The ID/IG ratios of ZIF-8/DW-CA and ZIF/TW-CA were 1.37 and 1.24, respectively, indicating that ZIF-8/TW-CA exhibited larger defects than ZIF-8/DW-CA, which can be attributed to the high degree of N-doping [40,66].Next, thermogravimetric analysis (TGA) was conducted to investigate the thermal properties and compare the ZIF-8 loading amounts of the ZIF-8/wood aerogels (Figure 4b).The decomposition of the ZIF-8/wood aerogels was observed to begin at approximately 240 • C, which can be attributed to thermal degradation of the cellulose content.The residual content of ZIF-8/TW-A (20%) was higher than that of ZIF-8/DW-A (12%), indicating the higher ZIF-8 loadings of ZIF-8/TW-A.This difference between their ZIF-8 loadings can be attributed to the different amounts of carboxyl groups from the TEMPO oxidation.To examine the specific surface area and pore-size distribution, we conducted argon adsorption-desorption measurements for the pristine wood, ZIF-8/DW-CA, and ZIF-8/TW-CA.The pristine wood hardly adsorbed argon and only slightly adsorbed argon towards the end of the measurement, indicating that the wood was only composed of macropores (Figure 4c and Table 1).
Nanomaterials 2023, 13, x degradation of the cellulose content.The residual content of ZIF-8/TW-A (20%) wa than that of ZIF-8/DW-A (12%), indicating the higher ZIF-8 loadings of ZIF-8/TW difference between their ZIF-8 loadings can be attributed to the different amount boxyl groups from the TEMPO oxidation.To examine the specific surface area an size distribution, we conducted argon adsorption-desorption measurements for tine wood, ZIF-8/DW-CA, and ZIF-8/TW-CA.The pristine wood hardly adsorbe and only slightly adsorbed argon towards the end of the measurement, indicating wood was only composed of macropores (Figure 4c and Table 1).Compared to those of ZIF-8/DW-CA (662.1 m 2 g −1 , 0.30 cm 3 g −1 ), ZIF-8/TW-CA ited a large specific surface area (785.8 m 2 /g) and pore volume (0.46 cm 3 g −1 ).Thes confirm that the high ZIF-8 loading mass owing to the TEMPO oxidation prom nanoporous structure of the wood-based CA.The pore-size distribution range 8/DW-CA and ZIF-8/TW-CA was 0.8-2.8nm, indicating that carbonization and ac processes led to the presence of micro-and mesopores in both wood-based CAs Table 1.BET surface area (S BET ), average pore volume (V m ), and pore-size distribution of the samples.

Samples
S BET (m 2 g −1 ) V m (cm Compared to those of ZIF-8/DW-CA (662.1 m 2 g −1 , 0.30 cm 3 g −1 ), ZIF-8/TW-CA exhibited a large specific surface area (785.8 m 2 /g) and pore volume (0.46 cm 3 g −1 ).These results confirm that the high ZIF-8 loading mass owing to the TEMPO oxidation promoted the nanoporous structure of the wood-based CA.The pore-size distribution range of ZIF-8/DW-CA and ZIF-8/TW-CA was 0.8-2.8nm, indicating that carbonization and activation processes led to the presence of micro-and mesopores in both wood-based CAs because of ZIF-8 and chemical activation process.(Figure 4d and Figure S5).Next, the adsorption ability of ZIF-8/TW-CA was investigated using RhB, which is a model dye.
We investigated the effect of the adsorption temperature and pH on the dye solution.The effect of temperature on RhB adsorption by the samples was investigated using a kinetic study at three different temperatures (Figure 5a and Table 2).The results reveal that there was no significant difference in the adsorption capacities (9.5, 10.1, and 10.0 mg g −1 at 293, 308, and 318 K) of ZIF-8/TW-CA at the three temperatures, implying that the adsorption temperature had no significant effect on the dye adsorption in the temperature range of 293-318 K. RhB is a zwitterion dye in which the ionic state depends on pH; therefore, RhB changes from a cation to zwitterion form when the pH exceeds 3.7 (pKa of RhB).Consequently, this can affect the electrostatic interaction with the adsorbent.As shown in Figure 5b, the removal efficiency of ZIF-8/TW-CA was maintained within the pH range of 3-11, suggesting that RhB molecules can interact with other bonds through various mechanisms, such as hydrophobic interactions (π-π bonds), hydrogen bonds, and cation-π bonds of ZIF-8/TW-CA, except electrostatic interactions [71].
Nanomaterials 2023, 13, x 10 We investigated the effect of the adsorption temperature and pH on the dye solu The effect of temperature on RhB adsorption by the samples was investigated using netic study at three different temperatures (Figure 5a and Table 2).The results reveal there was no significant difference in the adsorption capacities (9.5, 10.1, and 10.0 m at 293, 308, and 318 K) of ZIF-8/TW-CA at the three temperatures, implying that the sorption temperature had no significant effect on the dye adsorption in the tempera range of 293-318 K. RhB is a zwitterion dye in which the ionic state depends on pH; th fore, RhB changes from a cation to zwitterion form when the pH exceeds 3.7 (pKa of R Consequently, this can affect the electrostatic interaction with the adsorbent.As show Figure 5b, the removal efficiency of ZIF-8/TW-CA was maintained within the pH ran 3-11, suggesting that RhB molecules can interact with other bonds through various m anisms, such as hydrophobic interactions (π-π bonds), hydrogen bonds, and catio bonds of ZIF-8/TW-CA, except electrostatic interactions [71].Figure 5c shows the UV-VIS spectra of the RhB solution (10 mg L −1 ) after 24 h adsorption by ZIF-8/DW-CA and ZIF-8/DW-CA.The color of the RhB solution disappeared when ZIF-8/TW-CA was immersed, whereas the color remained in the case of ZIF-8/DW-CA, indicating the enhanced porosity of ZIF-8/TW-CA for dye adsorption.Compared to that of DW, the loading of ZIF-8, with a high surface area, on TW was higher, owing to the presence of carboxyl groups (Figure 4a).In addition, the nanoporous structure of the cell wall (Figure 2g) caused by TEMPO treatment could facilitate the efficient capture of dye molecules in the solution.These factors can increase the specific area and micro/mesopores of ZIF-8/TW-CA (Figure 4b and Table 1).Figure 5d describes the effect of the initial RhB concentration on the adsorption capacity of ZIF-8/TW-CA.In this study, we employed two well-known adsorption isotherm models (Langmuir and Freundlich) to evaluate the experimental results.The parameters of the Langmuir and Freundlich isotherms are summarized in Table S1.The Freundlich model was more suitable for the analysis of the adsorption isotherm, and it exhibited a high correlation coefficient (R 2 = 0.99).The maximum adsorption capacities (q max ) of balsa wood, ZIF-8/DW-CA, and ZIF-8/TW-CA were 43.15, 119.4,and 169.4 mg g −1 , respectively.Particularly, the adsorption capacity of ZIF-8/TW-CA for RhB was approximately 1.4 times higher than that of ZIF-8/DW-CA.Importantly, the ZIF-8/TW-CA exhibited a good adsorption capacity (169.4 mg/g) for RhB comparable to previously reported values of other adsorbents, including biomass-based activated carbons (35.7 to 161.8 mg/g) (Table 3) [71][72][73][74][75][76][77][78][79][80][81][82].The kinetic adsorption of ZIF-8/DW-CA and ZIF-8/TW-CA was observed for 24 h (Figure 5e and Table 2), and the result revealed that the pseudo-second-order kinetic model (R 2 = 0.99) for chemical adsorption was more suitable for explaining the experimental data.A recycling test was conducted to investigate the reusability of ZIF-8/TW-CA.The used adsorbent was washed several times with a mixed solution of DIW and ethanol (1:1, 60 • C) until no dye was released, and then immersed in a fresh RhB solution (10 mg L −1 ).As shown in Figure 5f, even after three adsorption rounds, there was only a slight difference in the removal efficiency (96%) of ZIF-8/TW-CA.This result demonstrates the good reusability of ZIF-8/TW-CA via a simple desorption method.Porous materials with high porosity and a good affinity for hydrophobic solvents can also be used for the removal of organic solvents from polluted water.Lastly, we tested the ability of ZIF-8/TW-CA for the removal of organic solvents (Figure S6), and the results revealed that it took just 3 and 15 s to remove n-hexane and chloroform from the surface of water and underwater, respectively.These results demonstrate the good affinity of ZIF-8/TW-CA for hydrophobic organic solvents and its usefulness for the removal of organic solvents from polluted water.Considering the cost-effectiveness, renewability, and eco-friendliness of the ZIF-8/wood-based CA, these functional wood-based nanocomposites can serve as a promising adsorbent platform for various practical applications.

Table 3 .
Comparison of the maximum adsorption capacity of various adsorbents for RhB.