Mesoporous Cu-Ni/Al₂O₄ catalyst of high surface area (176 m²g⁻¹) is synthesized through a simple hydrothermal reconstruction process by using low-cost activated alumina as the aluminate source without organic templates. The desired mesoporous structure of the catalyst is formed by the addition of Cu²⁺ and Ni²⁺ metal ions in the gel solution of the activated alumina followed by hydrothermal treatment at 70 °C and calcination at temperatures in the range of 600 to 800 °C. To consider the environmental concern, we found the concentration of the Cu²⁺ and Ni²⁺ ion in the residual filtrate is less than 0.1 ppm which satisfies the effluent standard in Taiwan (<1.0 ppm). The effects of the pH value, hydrothermal treatment time, and calcination temperature on the structure, morphology and surface area of the synthesized Cu-Ni/Al₂O₄ composites are investigated as well. In addition, the Cu-Ni/Al₂O₄ catalyst synthesized at pH 9.0 with a hydrothermal treatment time of 24 h and a calcination temperature of 600 °C is used for hydrogen production via the partial oxidation of methanol. The conversion efficiency is found to be >99% at a reaction temperature of around 315 °C, while the H₂ yield is 1.99 mol H₂/mol MeOH. The catalyst retains its original structure and surface area following the reaction process, and is thus inferred to have a good stability. Overall, the hydrothermal reconstruction route described herein is facile and easily extendable to the preparation of other mesoporous metal-alumina materials for catalyst applications. Full article

A new photocatalyst for CO₂ reduction has been presented. The photocatalyst was prepared from a combination of a commercial P25 with a mesopore structure and carbon spheres with a microporous structure with high CO₂ adsorption capacity. Then, the obtained hybrid TiO₂-carbon sphere photocatalysts were deposited on a glass fiber fabric. The combined TiO₂-carbon spheres/silica cloth photocatalysts showed higher efficiency in the two-electron CO₂ reduction towards CO than in the eight-electron reaction to methane. The 0.5 g graphitic carbon spheres combined with 1 g of TiO₂ P25 resulted in almost 100% selectivity to CO. From a practical point of view, this is promising as it economically eliminates the need to separate CO from the gas mixture after the reaction, which also contains CH₄ and H₂. Full article

This study presents core/shell Ag/SnO₂ nanowires (Ag/SnO₂NWs) as a new photocatalyst for the rapid degradation of organic compounds by the light from the visible range. AgNWs after coating with a SnO₂ shell change optical properties and, due to red shift of the absorbance maxima of the longitudinal and transverse surface plasmon resonance (SPR), modes can be excited by the light from the visible light region. Rhodamine B and malachite green were respectively selected as a model organic dye and toxic one that are present in the environment to study the photodegradation process with a novel one-dimensional metal/semiconductor Ag/SnO₂NWs photocatalyst. The degradation was investigated by studying time-dependent UV/Vis absorption of the dye solution, which showed a fast degradation process due to the presence of Ag/SnO₂NWs photocatalyst. The rhodamine B and malachite green degraded after 90 and 40 min, respectively, under irradiation at the wavelength of 450 nm. The efficient photocatalytic process is attributed to two phenomenon surface plasmon resonance effects of AgNWs, which allowed light absorption from the visible range, and charge separations on the Ag core and SnO₂ shell interface of the nanowires which prevents recombination of photogenerated electron-hole pairs. The presented properties of Ag/SnO₂NWs can be used for designing efficient and fast photodegradation systems to remove organic pollutants under solar light without applying any external sources of irradiation. Full article

Titanium nanotubes were hydrothermally synthesized via a two-step method for ODS (oxidative desulfurization). The catalysts’ structures were characterized by XRD (X-ray diffraction), FT-IR, UV-Vis (UV-Vis diffuse reflectance spectra), NH₃-TPD, etc. The effects of O/S molar ratio and catalyst dosage, etc., were systematically investigated. The catalyst exhibited remarkable performance, so that the removal of DBT (dibenzothiophene) was nearly 100% under the optimal conditions in 10 min. Also, the catalysts could be easily reused for six consecutive cycles. The hydrogen-assisted thermocatalytic mechanism over titanium nanotubes for ODS was also studied and an effective reactant concentration (ERC) number of 70.8 was calculated. Full article

In this work, we describe two different biotechnological processes that provide the natural flavour dihydrocoumarin in preparative scale. Both the presented approaches are based on the enzyme-mediated reduction of natural coumarin. The first one is a whole-cell process exploiting the reductive activity of the yeast Kluyveromyces marxianus, a Generally Recognized As Safe (GRAS) microorganism that possesses high resistance to the substrate toxicity. Differently, the second is based on the reduction of natural coumarin by nicotinamide adenine dinucleotide phosphate (NADPH) and using the Old Yellow Enzyme reductase OYE2 as catalyst. NADPH is used in catalytic amount since the co-factor regeneration is warranted employing an enzymatic system based on glucose oxidation, in turn catalysed by a further enzyme, namely glucose dehydrogenase (GDH). Both processes compare favourably over the previously reported industrial method as they work with higher coumarin concentration (up to 3 g/L for the enzymatic process) yet allowing the complete conversion of the substrate. Furthermore, the two approaches have significant differences. The microbial reduction is experimentally simple but the isolated dihydrocoumarin yield does not exceed 60%. On the contrary, the enzymatic approach requires the use of two specially prepared recombinant enzymes, however, it is more efficient, affording the product in 90% of isolated yield. Full article

Metal Fe is one of the phases existing on iron-based catalysts for a high-temperature water gas shift reaction (WGSR), but research on the activity of metal Fe in WGSR is almost not reported. In this work, the density functional theory (DFT) method was used to systematically study the reaction activity and mechanisms of WGSR on metal Fe (110), including the dissociation of H₂O, the transformation of CO and the formation of H₂, as well as the analysis of surface electronic properties. The results show that (1) the direct dissociation of H₂O occurs easily on Fe (110) and the energy barrier is less than 0.9 eV; (2) the generation of CO₂ is difficult and its energy barrier is above 1.8 eV; (3) H migrates easily on the Fe surface and the formation of H₂ also occurs with an energy barrier of 1.47 eV. Combined with the results of Fe₃O₄, it can be concluded that the active phase should be Fe₃O₄ with O vacancy defects, and the iron-rich region plays an important role in promoting the formation of H₂ in WGSR. Full article

Here, we report the fabrication of nZVI by the wet chemical technique in the presence of ethanol using ferric iron and sodium borohydride as the reducing agents under ambient conditions. The obtained nZVI particles are mainly in a zero-valent oxidation state and do not undergo significant oxidation for several weeks. The structural and morphological parameters of nZVI were investigated by using UV, XRD, SEM, EDX, TEM, and DLS analysis. The optical nature, bandgap energy, and absorption edge were all revealed by the UV–visible spectrum. The phase development and crystallinity of nZVI particles were shown by the XRD pattern. The morphological investigation revealed that the nanoparticles were spherical with an average size of 34–110 nm by using ImageJ software, and the elemental analysis was analyzed using EDX. Furthermore, the catalytic treatment performance of domestic wastewater was evaluated in terms of pH, COD (chemical oxygen demand) solubilization, total solids (TS), volatile solids (VS), phosphorous, and total nitrogen (TN) reduction under aerobic and anaerobic operating conditions. The effluent was subjected to a process evaluation with a different range (100–500 mg/L) of nZVI dosages. The COD solubilization and suspended solids reduction were significantly improved in the anaerobic condition in comparison to the aerobic condition. Furthermore, the effect of nZVI on phosphorous (PO₄³⁻) reduction was enhanced by the electrons of iron ions. The high concentration of nZVI dosing has a positive impact on COD solubilization and phosphorous removal regardless of the aeration condition with 400 mg/L of nZVI dosage. Full article

Global demand for plastics has increased steadily alongside industrial development. Despite their versatility and convenience, environmental pollution caused by plastics are a major issue. With a reduction in the market size of plastics being seemingly impossible, bioplastics may become key to tackle this issue. Among a wide range of sources of bioplastics, microalgae have come into the limelight. While abundant and valuable components in microalgae have the potential to replace preexisting plastics, complex processes and low cost performances have prevented them from entering the market. In this study, we examined techniques for biocomposites in which polymers are blended with microalgae. We focused on microalgae-based biocomposite blending processed from the perspective of functionality and cost performance. Full article

Ofloxacin is a highly efficient and widely used antibiotic drug. It is classified as a refractory pollutant due to its poor biodegradability. Consequently, it is commonly found in water sources, requiring efficient methods for its removal. Advanced oxidation processes (AOPs) offer efficient alternatives since those yield complete degradation not achieved in adsorption or membrane processes. Previous studies suggest ofloxacin degradation follows a pseudo-first or -second order processes, whereas for full removal of refractory pollutants—lower pseudo-orders are required. Monitoring the actual “pseudo-order” degradation kinetics of ofloxacin is needed to evaluate any proposed AOP process. This study presents a simple procedure to evaluate pseudo-orders of AOPs. Photolysis of 20 μM ofloxacin solutions follow pseudo-zero order kinetics, with half-life times (t_1/2) of approx. 60 min. TiO₂ heterogenous catalysts have been shown to have no influence at low concentrations (0.2 mg L⁻¹), but a significant reduction of half-life time (t_1/2 = 20 min) and increase in pseudo-order (0.8) is measured at 2.0 mg L⁻¹. Similar results are obtained with homogenous catalysis by 2.0 mg L⁻¹ H₂O₂. The combination of H₂O₂ and TiO₂ catalysts shows additional reduction in half-time life with increase in the pseudo-order to 1.2. The conclusions are (1) heterogenous and homogenous photocatalysis can effectively degrade ofloxacin, (2) combined photocatalysis yields higher pseudo-order, being less prone to achieve full removal, and (3) analysis of specific pseudo-orders in AOPs of refractory pollutants helps to further elucidate the efficiency of the processes. Full article

In this study, we develop the optimum composition of copper oxide/ruthenium oxide and multi-walled carbon nanotubes (CuO/RuO₂/MWCNTs) ternary nanocomposite via a hydrothermal method as an efficient electrode material for supercapacitor applications. The ratio between CuO and RuO₂ varied to improve the electrochemical performance of the electrode. The synthesized nanocomposites are analyzed by high-resolution scanning electron microscopy (HR-SEM), thermo gravimetric analyzer (TGA) and electrochemical impedance spectroscopy (EIS). Furthermore, the elemental composition is analyzed by energy dispersive X-ray (EDX) spectroscopy and the specific capacitance was analyzed by cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) methods. The electrochemical investigations is conducted in a three-electrode system and the sample is attached on a stainless steel plate as the working electrode; platinum wire works as the counter electrode and Ag/AgCl electrode as the reference electrode, adopting 3 M (NH₄)₂SO₄ as the electrolyte. The resultant of CuO/RuO₂/MWCNT nanocomposite with 7 wt% Cu and 20 wt% Ru was found to perform the highest specific capacitance of 461.59 F/g in a current density of 1 A/g. Full article

A new type of Gd₂BiTaO₇ nanocatalyst (GBT) was synthesized by a high-temperature solid-phase method, and a heterojunction photocatalyst, which was composed of GBT and silver phosphate (AP), was prepared by the facile in-situ precipitation method for the first time. The photocatalytic property of GBT or the Ag₃PO₄/Gd₂BiTaO₇ heterojunction photocatalyst (AGHP) was reported. The structural properties of GBT and AGHP were characterized by an X-ray diffractometer, scanning electron microscope–X-ray energy dispersive spectra, an X-ray photoelectron spectrograph, a synchrotron-based ultraviolet photoelectron spectroscope, a Fourier transform infrared spectrometer, an UV-Vis diffuse reflectance spectrophotometer and an electron paramagnetic resonance spectrometer. The results displayed that GBT was well crystallized with a stable cubic crystal system and space group Fd3m. The lattice parameter or band gap energy of GBT was found to be a = 10.740051 Å or 2.35 eV, respectively. After visible light irradiation of 30 min, the removal rate of bisphenol A (BPA) reached 99.52%, 95.53% or 37.00% with AGHP as the photocatalyst, with Ag₃PO₄ and potassium persulfate (AP-PS) as photocatalysts or with N-doped TiO₂ (NT) as a photocatalyst, respectively. According to the experimental data, it could be found that the removal rate of BPA with AGHP as a photocatalyst was 2.69 times higher than that with NT as a photocatalyst. AGHP showed higher photocatalytic activity for photocatalytic degradation of BPA under visible light irradiation compared with GBT or AP-PS or NT. The removal rate of total organic carbon (TOC) was 96.21%, 88.10% or 30.55% with AGHP as a photocatalyst, with AP-PS as photocatalysts or with NT as a photocatalyst after visible light irradiation of 30 min. The above results indicated that AGHP possessed the maximal mineralization percentage ratio during the process of degrading BPA compared with GBT or AP-PS or NT. The results indicated that the main oxidation radical was ^•OH during the process of degrading BPA. The photocatalytic degradation of BPA with AGHP as a photocatalyst conformed to the first-order reaction kinetics. This study provided inspiration for obtaining visible light-responsive heterojunction photocatalysts with high catalytic activity and efficient removal technologies for organic pollutants and toxic pollutants, and as a result, the potential practical applications of visible light-responsive heterojunction photocatalysts were widened. The subsequent research of thin-film plating of the heterojunction catalysts and the construction of complete photoluminescent thin-film catalytic reaction systems, which utilized visible light irradiation, could provide new technologies and perspectives for the pharmaceutical wastewater treatment industry. Full article

In this paper, two novel procedures based on powder sedimentation, thermal treatment, and galvanostatic deposition were proposed for the preparation of porous cobalt ferrite (CoFe₂O₄) coatings with a metallic and organic binder for use as catalysts in the oxygen evolution reaction (OER). The electrochemical properties of the obtained electrode materials were determined as well, using both dc and ac methods. It was found that cobalt ferrite coatings show excellent electrocatalytic properties towards the oxygen evolution reaction (OER) with overpotential measured at a current density of 10 mAcm⁻² from 287 to 295 mV and a Tafel slope of 35–45 mVdec⁻¹. It was shown that the increase in the apparent activity of the CoFe₂O₄ coatings with an organic binder results mainly from a large electrochemically active area. Incorporation of the nickel binder between the CoFe₂O₄ particles causes an increase in both the conductivity and the electrochemically active area. The Tafel slopes indicate that the same rate-determining step controls the OER for all obtained coatings. Furthermore, it was shown that the CoFe₂O₄ electrodes exhibit no significant activity decrease after 28 h of oxygen evolution. The proposed coating preparation procedures open a new path to develop high-performance OER electrocatalysts. Full article

Catalytic aerobic oxidation of benzyl alcohol (BnOH) to benzaldehyde (PhCHO) over supported noble metal catalysts has grabbed the attention of researchers due to the critical role of PhCHO in numerous industrial syntheses. In the present study, a novel catalyst, Pd-P alloy supported on aminopropyl-functionalized mesoporous silica (NH₂-SiO₂), was prepared through in situ reduction and characterized by BET-BJH analysis, SEM, TEM, XRD, FTIR, TG-DTA, and XPS. Chemical properties and catalytic performance of Pd-P/NH₂-SiO₂ were compared with those of Pd° nanoparticles (NPs) deposited on the same support. Over Pd-P/NH₂-SiO₂, the BnOH conversion to PhCHO was much higher than over Pd°/NH₂-SiO₂, and significantly influenced by the nature of solvent, reaching 57% in toluene at 111 °C, with 63% selectivity. Using pure oxygen as an oxidant in the same conditions, the BnOH conversion increased up to 78%, with 66% selectivity. The role of phosphorous in improving the activity may consist of the strong interaction with Pd that favours metal dispersion and lowers Pd electron density. Full article

This work presents the effect of Co loading on the performance of CNR115 carbon-supported catalysts in the continuous-flow chemoselective hydrogenation of 2-methyl-2-pentenal for the obtention of 2-methylpentanal, an intermediate in the synthesis of the sedative drug meprobamate. The Co loading catalysts (2, 6, 10, and 14 wt.%) were characterized by Brunauer–Emmett–Teller (BET) surface area analysis, transmission electron microscopy (TEM), H₂ temperature-programmed reduction (H₂-TPR), temperature-programmed desorption of hydrogen (H₂-TPD) analysis, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy for selected samples, and have been studied as hydrogenation catalysts at different pressure and temperature ranges. The results reveal that a certain amount of Co is necessary to achieve significant conversion values. However, excessive loading affects the morphological parameters, such as the surface area available for hydrogen adsorption and the particle size, preventing an increase in conversion, despite the increased presence of Co. Moreover, the larger particle size, caused by increasing the loading, alters the chemoselectivity, favouring the formation of 2-methyl-2-pentenol and, thus, decreasing the selectivity towards the desired product. The 6 wt.% Co-loaded material demonstrates the best catalytic performance, which is related to the formation of NPs with optimum size. Almost 100% selectivity towards 2-methylpentanal was obtained for the catalysts with lower Co loading (2 and 6 wt.%). Full article

In this paper is reported the synthesis of N,N′ hydroxy derivative of NHC silver (3a–4a) and gold(I) (3b–4b) complexes of general formula [M(NHC)₂]⁺ [MX₂]⁻. All compounds were characterized by spectroscopic and analytic techniques. The complexes turned out to be effective in both catalytic and biological applications. They catalyzed the coupling of aldehyde, piperidine, and phenylacetylene in A³-reaction to produce propargylamines and showed antimicrobial activity. In fact, minimal inhibition concentration (MIC) tests with Gram-positive and Gram-negative bacteria demonstrated that the silver compounds are selective toward E. coli, whereas the gold analogues are active against S. aureus. Moreover, the N,N′ hydroxy derivative of NHC silver complexes 3a and 4a exhibited good anticancer activity on the HeLA cancer cells (3a-IC₅₀ = 12.2 ± 0.1 µM, 4a-IC₅₀ = 11.9 ± 1.2 µM), whereas gold complex 4b displayed good anticancer activity towards the MCF-7 cells (IC₅₀ = 12.2 ± 1.2 µM). Full article