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Journal of Energy Chemistry 2025年第1期100卷 317-326页

作者： Binglu Deng Jie Shen Jinxing Lu Chuqiang Huang Zhuoyuan Chen Feng Peng Yunpeng Liu School of Materials Science and Hydrogen Energy Foshan University School of Chemistry and chemical engineering Guangzhou University Guangdong key laboratory for Hydrogen Energy Technologies

Seawater electrolysis is a promising approach for sustainable energy without relying on precious ***,the large-scale seawater electrolysis is hindered by low catalytic efficiency and severe anode corrosion caused by the harmful *** contrast to the oxygen evolution reaction （OER）and chlorin ion oxidation reaction （ClOR）,glycerol oxidation reaction （GOR） is more thermodynamically and kinetically favorable ***,a Ru doping cobalt phosphide （Ru-CoP2） is proposed as a robust bifunctional electrocatalyst for seawater electrolysis and GOR,for the concurrent productions of hydrogen and value-added *** in situ and ex situ characterization analyses demonstrated that Ru doping featured in the dynamic reconstruction process from Ru-CoP2to Ru-CoOOH,accounting for the superior GOR *** coupling GOR with hydrogen evolution was realized by employing Ru-CoP2as both anode and cathode,requiring only a low voltage of 1.43 V at 100 mA cm-2,which was 250 m V lower than that in alkaline *** work guides the design of bifunctional electrocatalysts for energy-efficient seawater electrolysis coupled with biomass resource upcycling.

关键词： Glycerol electrooxidation Hydrogen evolution Ru doping Cobalt phosphide Bifunctional electrocatalysts

Boosting hydrocarbon conversion via Cu-doping induced oxygen vacancies on CeO2 in CO2 electroreduction

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Journal of Energy Chemistry 2025年第1期100卷 66-76页

作者： Lei Xue Tong Shi Chenhui Han Heng Zhang Fenrong Liu Haorun Li Yan Wang Xiaojun Gu Shanghong Zeng Inner Mongolia key laboratory of Chemistry and Physics of Rare Earth Materials School of Chemistry and Chemical Engineering Inner Mongolia University State key laboratory of Coal Conversion Institute of Coal Chemistry Chinese Academy of Sciences Institute of Catalysis Department of Chemistry Zhejiang University National key laboratory of Baiyunobo Rare Earth Resource Research and Comprehensive Utilization Baotou Research Institute of Rare Earths

Conversion of CO2back to hydrocarbons is the most direct way of closing the“carbon cycle”,and its significance is further enlarged if this process is driven by renewable energies such as ***,precisely controlling the product selectivity towards hydrocarbons against the competitive hydrogen evolution remains challenging,especially for Cu-based ***,we report a novel defect engineering strategy,by which Cu-doping-induced oxygen vacancies on CeO2nanorods were effectively created,with adjustable vacancy/Cu *** resulting optimum catalyst shows up to 79% catalytic current density to hydrocarbons （excluding CO）,with 49% faradaic efficiency to *** and density functional theory unveil that the ratio between oxygen vacancy and Cu affects significantly the formation of*CHO and activation of H2O,which leads to the following deep hydrogenation to *** findings may spur new insights for designing and developing more controllable chemical process relevant to CO2utilization.

关键词： Oxygen vacancy Hydrocarbon production Reaction mechanism

Preparation of a mesoporous sorption complex catalyst and its evaluation in reactive sorption enhanced reforming

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Journal of zhejiang university-Science A(Applied Physics & engineering) 2013年第12期14卷 915-922页

作者： Fan ZHANG Qi TANG Su-fang WU key laboratory of biomass chemical engineering of ministry of education Zhejiang University Department of chemical and Biological engineering Zhejiang University

A mesoporous sorption complex catalyst was prepared by pore-forming modification and evaluated by the COz reactive sorption enhanced reforming （ReSER） process, which is used to produce hydrogen from methane. Three samples of polyethylene glycol （PEG） with molecular weights between 2000 and 20 000 were added as templates into a mixed slurry to create catalysts with different pore properties by further formation and calcination. The pore characteristics determined by Brunauer- Emmett-Teller （BET） analysis showed that one of the mesoporous catalysts, named M-NiAICa-6000, had a pore size of 9.2 nm and a surface area of 70.52 m2/g and the CO2 sorption capacity of this catalyst was 44% higher than that of the catalyst without the PEG 6000 modification. The catalyst was evaluated in the ReSER process in a fixed-bed reactor system at 0.1 MPa and 600 C with an H20/CH4 molar ratio of 4. An H2 concentration of 94.2% and a CH4 conversion of 86.0% were obtained at a carbon space velocity of 1700 h 1 while CO2 was hardly detected.

关键词： Hydrogen Ni catalyst Mesoporous Steam methane reforming CO2 sorption

High performance n^+p-Si/Ti/NiS_xO_y photocathode for photoelectrochemical hydrogen evolution in alkaline solution

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Journal of Energy Chemistry 2019年第3期28卷 101-107页

作者： Qing Jia Chunlin Yu Wei Liu Guokui Zheng Chaojun Lei Lecheng Lei Xingwang Zhang key laboratory of biomass chemical engineering of ministry of education College of Chemical and Biological Engineering Zhejiang University

Silicon, as a promising semiconductor for fabricating photocathode toward photoelectrochemical hydrogen evolution reaction(PEC-HER), should be improved in light harvesting ability and catalytic kinetics to obtain high PEC performance. Herein, a novel amorphous Nickel Oxysulfide(NiS_xO_y) film is effectively integrated with a Ti protected n^+p-Si micropyramid photocathode by the electrodeposition method. The fabricated n^+p-Si/Ti/Ni SxOyphotocathode exhibits excellent PEC-HER performance with an onset potential of 0.5 V(at J =-0.1 mA/cm^2), a photocurrent density of-26 mA/cm^2 at 0 V vs. RHE, and long term stability of six hours in alkaline solution(pH ≈ 14). The synergy of unique n^+p-Si micropyramid architectures(omnidirectional broadband light harvesting ability), novel amorphous NiS_xO_y catalyst(high HER electrocatalytic activity and good optical transparency) results in the high performance of n^+pSi/Ti/Ni S_xO_y. This work offers a novel strategy for effectively integrating electrocatalysts with semiconductor to design efficient photoelectrode toward PEC water splitting.

关键词： Photoelectrochemical water splitting Silicon Photocathode Nickel oxysulfide

Hybridization of metal–organic framework and monodisperse spherical silica for chromatographic separation of xylene isomers

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Chinese Journal of chemical engineering 2019年第4期27卷 818-826页

作者： Bixuan Gao Minhui Huang Zhiguo Zhang Qiwei Yang Baogen Su Yiwen Yang Qilong Ren Zongbi Bao key laboratory of biomass chemical engineering of the ministry of education College of Chemical and Biological EngineeringZhejiang University

Metal–organic frameworks(MOFs) packed in the column have been a promising candidate as the stationary phase for high performance liquid chromatography(HPLC). However, the direct packing of irregular MOF powder could raise some problems like high back pressure and low column efficiency in the HPLC separation. In this work, UiO-66 capable of separating xylenes was supported effectively on the surface of the monodisperse spherical silica microspheres by one-pot method. The hybridization of Ui O-66 and silica microspheres(termed UiO-66@SiO2 shell–core composite) was prepared by stirring the suspension of the precursors of Ui O-66 and\\COOH terminated silica in the N,N-dimethylformamide with heating. The shell–core composite material UiO66@SiO2 was characterized by SEM, TEM, PXRD and FTIR. Then, it was used as a packing material for the chromatographic separation of xylene isomers. Xylene isomers including o-xylene, m-xylene and p-xylene were efficiently separated on the column with high resolution and good reproducibility. Moreover, the Ui O-66@SiO2 shell–core composites packed column still remained reverse shape selectivity as Ui O-66 possessed, and the retention of xylenes was probably ascribed to the hydrophobic effect between analytes and the aromatic rings of the Ui O-66 shell. The Ui O-66@SiO2 shell–core composites obtained in this study have some potential for the separation of structural isomers in HPLC.

关键词： Adsorption Chromatography Separation Hybridization Metal–organic framework Silica

Characteristics of Electrode-Water-Electrode Discharge and its Application to Water Treatment

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Plasma Science and Technology 2014年第5期16卷 479-485页

作者：王小平李中坚张兴旺雷乐成 key laboratory of biomass chemical engineering of ministry of education Department of Chemical and Biological EngineeringZhejiang University

Atmospheric air discharge above the surface of water is an effective method for water *** leakage current and Joule heating of water are reduced by the air gap,which raises the energy efficiency of the water ***,the application of this kind of discharge is limited by a pair of conflicting factors：the chemical efficiency grows as the discharge gap distance decreases,while the spark breakdown voltage decreases as the gap distance *** raise the spark breakdown voltage and the chemical efficiency of atmospheric pressure water surface discharge,both the high-voltage electrode and the ground electrode are suspended above the water surface to form an electrode-water-electrode discharge *** this system,there are two potential discharge directions：from one electrode to another directly,and from the electrodes to the water *** first step in utilizing the electrode-water-electrode discharge is to find out the discharge direction transition *** this paper,the discharge direction transition criterions of spark discharge and streamer discharge are *** comparing the discharge characteristics and the chemical efficiencies,the discharge propagating from the electrodes to the water surface is proved to be more suitable for water treatment than that propagating directly between the electrodes.

关键词： water treatment electrode-water-electrode discharge discharge direction discharge intensity chemical efficiency

engineering atomic Rb-N configurations to tune radical pathways for highly selective photocatalytic H2O2 synthesis coupled with biomass valorization

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Journal of Energy Chemistry 2025年第1期100卷 215-225页

作者： Jiaye Li Shuang Pan Yihuang Chen Qiong Liu College of Chemistry and Materials engineering Wenzhou University Guangdong Provincial key laboratory of chemical Measurement and Emergency Test Technology (China) Institute of Analysis Guangdong Academy of Sciences (China National Analytical CenterGuangzhou)

Photocatalytic oxygen reduction for hydrogen peroxide （H2O2） synthesis presents a green and costeffective production ***,achieving highly selective H2O2synthesis remains challenging,necessitating precise control over free radical reaction pathways and minimizing undesirable oxidative ***,we report for the visible light-driven simultaneous co-photocatalytic reduction of O2to H2O2and oxidation of biomass using the atomic rubidium-nitride modified carbon nitride（CNRb）.The optimized CNRb catalyst demonstrates a record photoreduction rate of 8.01 mM h-1for H2O2generation and photooxidation rate of 3.75 mM h-1for furfuryl alcohol to furoic acid,achieving a remarkable solar-to-chemical conversion （SCC） efficiency of up to 2.27%.Experimental characterizations and DFT calculation disclosed that the introducing atomic Rb–N configurations allows for the high-selective generation of superoxide radicals while suppressing hydroxyl free radical *** is because the Rb–N serves as the new alternative site to perceive a stronger connection position for O2adsorption and reinforce the capability to extract protons,thereby triggering a high selective redox product *** study holds great potential in precisely regulating reactive radical processes at the atomic level,thereby paving the way for efficient synthesis of H2O2coupled with biomass valorization.

关键词： Atomic economy Radical pathway regulation Rubidium atom coordination biomass valorization

Adsorption behaviors of avian immunoglobulins and purification of immunoglobulin Y from chicken serum with mixed-mode resins

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Chinese Journal of chemical engineering 2019年第3期27卷 514-518页

作者： Yingdi Luo Qilei Zhang Shanjing Yao Dongqiang Lin key laboratory of biomass chemical engineering of ministry of education College of Chemical and Biological Engineering Zhejiang University

The importance of immunoglobulin Y(IgY) as a specific antibody equivalent to mammalian immunoglobulin G(IgG) is well recognized. However, production of highly purified IgY is still difficult due to the lack of specific purification methods. In this study, adsorption behaviors of Ig Y on four mixed-mode resins with functional ligands of 4-mercatoethyl-pyridine(MEP), 2-mercapto-1-methyli-midazole(MMI), 5-aminobenzi-midazole(ABI) and tryptophan-5-aminobenzi-midazole(W-ABI) were evaluated. The results showed that high adsorption ratio were found at p H 6.0–7.0 with little adsorption under acidic conditions. The resin with ABI ligand was then used to separate IgY from immunized chicken serum. An efficient process with Ig Y purity of 95% and recovery of 90% was developed after optimization of loading and elution p H and injection volume. The biological activity of the purified Ig Y was fully maintained. These results indicated that mixed-mode chromatography with specially-designed ligands has great potential for the separation of Ig Y from crude feedstock.

关键词： Mixed-mode chromatography Immunoglobulin Y Adsorption selectivity Separation

Current–voltage characteristics of hydrogen DC plasma torches with different sizes in an external axial magnetic field

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Chinese Physics B 2015年第6期24卷 425-428页

作者：马杰闻光东苏宝根杨亦文任其龙 key laboratory of biomass chemical engineering of ministry of education College of Chemical and Biological EngineeringZhejiang University

Current-voltage （l-V） characteristics of hydrogen DC plasma torches with different sizes in an external axial magnetic field under atmospheric pressure are reported. Three anodes with different diameters are adopted in a 50-kW torch： 25 mm, 30 mm, and 35 nun, respectively. Two different diameters of anodes, that is, 100 mm and 130 mm, are adopted in a 1-MW plasma torch. The arc voltage shows a negative trend with the increase of arc current under the operating regimes. On the contrary, arc voltage shows a positive trend as the flow rate of carder gas increases, and a similar trend is found with increasing the external magnetic flux density. A similarity formula is constructed to correlate the experimental data of the torches mentioned above. Linear fitting shows that the Pearson correlation coefficient is 0.9958.

关键词： magnetically rotating hydrogen plasma I-V characteristics similarity theory

Preparation and evaluation of mixed-mode resins with tryptophan analogues as functional ligands for human serum albumin separation

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Chinese Journal of chemical engineering 2017年第7期25卷 898-905页

作者： Qici Wu Qilei Zhang Shiwen Xu Cheng ong Ge Shanjing Yao Dongqiang Lin key laboratory of biomass chemical engineering of ministry of education College of Chemical and Biological EngineeringZhejiang UniversityHangzhou 310027China

Five tryptophan analogues with a hydrophobic indole ring and an amino group on each molecule were used as functional ligands of mixed-mode resins for human serum albumin(HSA) purification. Their adsorption performance was evaluated and the effects of p H and salt addition on HSA adsorption were studied. The resins prepared showed typical p H-dependent adsorption and the highest adsorption capacity and affinity were found at pH 5.0for all the resins tested. The saturated adsorption capacity was 138.02 mg·g^(-1)with the tryptaminefunctionalized resin, which significantly decreased at p H below 4.0 due to electrostatic repulsion between ligands and HSA. Moreover, the addition of Na Cl or(NH_4)_2SO_4in media reduced HSA adsorption capacity, although the two salts showed different affecting profiles. The tryptamine-functionalized resin showed the best salt-tolerant performance, and its high adsorption capacity was maintained under high salt concentrations. In addition, the five resins prepared showed good adsorption selectivity for recombinant HSA from Pichia pastoris broth. Molecular docking results between tryptamine and HSA indicated that tryptamine was favorable to bind on Site II(indole-binding site) of HSA.

关键词： Adsorption Human serum albumin Mixed-mode chromatography Tryptamine Tryptophan analogue