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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

Efficient degradation of norfloxacin by CoWO4/CS/BiOCl-10 Z-type heterojunction photocatalysts based on hydrogen bonding and interfacial interaction

Xinyan Wang,Yuting Zhang,Jian Zhang,Chengpeng Shao,Jiaxing Yang,Yuning Zhang,Ruoyi Li,Zheng Xing

In this study, a Z-type heterojunction photocatalyst CoWO 4 /CS/BiOCl-10 was constructed by hydrothermal synthesis for the efficient removal of norfloxacin (NOR) contaminants in water. X-ray photoelectron spectroscopy (XPS) combined with Fourier transform infrared spectroscopy (FT-IR) confirmed that the hydroxyl group in the chitosan (CS) molecule was bonded with the oxygen atom on the surface of CoWO 4 through hydrogen bonding to form a directional charge transport channel, which greatly improved the photocatalytic degradation efficiency of CoWO 4 /CS/BiOCl-10, and the degradation rate was as high as 98.30 % within 90 min under 300 W xenon lamp irradiation. Optoelectronic measurements show that the interfacial potential difference drives electrons to migrate along the Z-path. Density functional theory (DFT) and liquid chromatography-mass spectrometry (LC-MS) were used to identify intermediates in the NOR degradation process, revealing the degradation pathway of NOR through piperazine ring cleavage and defluorination. The kinetics of NOR degradation intermediates were revealed using two-dimensional correlation spectroscopy (2DCOS) techniques. Rice seed germination experiments have shown that the degraded NOR solution is virtually non-toxic, greatly reducing the environmental impact. This study provides a new strategy for the development of efficient photocatalytic systems through the synergistic regulation mechanism of hydrogen bonding and heterojunction.

研究领域: 环境科学 · 材料科学 · 光催化 · 水处理 · 化学工程 · 光谱学 · 毒理学
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NEW JOURNAL OF CHEMISTRY · 2021 ·Vol. 45 ·期 32 ·14406-14413 · IF 3.591

Conversion of glucose to levulinic acid and upgradation to γ-valerolactone on Ru/TiO2 catalysts

Yubo Liu,Guoqiang Ding,Guoping Zhao,Haohao She,Yulei Zhu,Yong Yang

Combining glucose dehydration and the subsequent hydrogenation in one pot is a preferable approach for process development as such a method allows in situ generation of the reactive intermediate to undergo further reaction without extra energy-intensive separation. Herein, phosphotungstic acid and various types of titania (anatase, rutile, P25) supported Ru-based catalysts were considered as the dehydration and hydrogenation catalysts, respectively. Modulating the different reactant media (N2, H2), various products were obtained with GBL–H2O as the solvent. A considerable yield (42%) of levulinic acid (LA) and γ-valerolactone (GVL) (40%) were obtained in nitrogen and subsequent hydrogen. Ru/TiO2 (rutile) was the favorable hydrogenation catalyst among the three types of Ru/TiO2. Meanwhile, a certain amount of sorbitol (36%) was obtained in pure hydrogen. The hydrogenation of glucose is more likely to occur than the glucose dehydration. The physicochemical properties of the catalysts were characterized by XRD, BET, TPR, STEM and in situ CO/FT-IR, and the results show that well-dispersed Ru particles are located on the rutile crystallites, which facilitated the hydrogenation of LA. A strong metal support interaction (SMSI) was responsible for the various microstructure properties and the different hydrogenation reactivity. This work allows a better understanding of the reaction paths of glucose conversion.

研究领域: 催化 · 化学工程 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Synthesis of bimetallic NbCo-piperazine catalyst and study on its advanced redox treatment of pharmaceuticals and personal care products by activation of permonosulfate

Hao Zhu,Shunyan Ning,Zengzhiqiang Li,Xinpeng Wang,Toyohisa Fujita,Yuezhou Wei,Xiangbiao Yin

Here, a nano disc-shaped bimetallic organic framework (NbCo-piperazine) was prepared by the solvothermal method for the activation of PMS for the degradation of contaminants. The effects of Nb/Co ratio, synthesis time and temperature on the morphology, structure and performance of the NbCo-piperazine catalyst were characterized by XRD, FT-IR, SEM-EDS and TEM. The optimum conditions for NbCo-PZ to activate PMS degradation of tetracycline were investigated by adjusting the dosage of catalyst, tetracycline concentration, pH and PMS concentration. The catalytic performance of NbCo-PZ in the presence of co-existing anions (Cl − , NO 3 – , HCO 3 2– , H 2 PO 4 − ) was also evaluated. XPS explained that cyclic changes in the valence states of Nb 4+ /Nb 5+ and Co 2+ /Co 3+ accelerated the activation of the PMS degradation process. EPR results showed the presence of free radicals (SO 4 ·− , ·OH and O 2 ·− ) and non-free radicals ( 1 O 2 ) in the degradation process, with free radicals playing a major role in the degradation process. The degradation rate of tetracycline after three cycles was 92.2%. In addition, NbCo-piperazine showed good catalytic performance for other organic pollutants such as methyl blue, tylosin tartrate and tetracycline with the degradation rate of 97.8%, 95.2% and 95.5%, respectively. Moreover, it also has good catalytic properties in various water systems such as river water and sea water.

CAS / MDL: 3317-61-1
研究领域: 环境化学 · 催化 · 水处理 · 材料科学
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MICROCHEMICAL JOURNAL · 2024 · IF 4.9

Advanced applications of spectral technology combined with chemometrics in rapid quantitative analysis and holistic quality evaluation of Cortex Fraxini

Mengyao Chen,Chunling Yin,Leqian Hu,Xinyao Lin,Liuchuang Zhao,Zhimin Liu,Peng Li

Quality of Cortex Fraxini is closely related to its clinical efficacy and drug safety. Traditional quality assessment methods are either non-objective or time-consuming. It is imperative to establish a rapid method for quality detection and evaluation of Cortex Fraxini . In this study, fourier transform infrared spectroscopy (FT-IR) and near-infrared spectroscopy (NIR) combined with chemometrics were used for rapid quantitative analysis of the main active components in Cortex Fraxini . Partial least squares regression (PLSR) combined with variable select by competitive adaptive reweighted sampling (CARS) algorithm gave rise to good predictions of the content of the three active components with R 2 values greater than 0.98. Furthermore, the quality evaluation results of Cortex Fraxini cannot be simply derived from data on the content of active ingredients. This study used technique for order preference by similarity to an ideal solution (TOPSIS) method and consistency analysis to evaluate the quality of Cortex Fraxini from five geographical origins. Two methods respectively realized the quality superiority ranking and quality consistency grading of Cortex Fraxini samples. The evaluation results showed that Cortex Fraxini derived from SN had the best performance in quality and was consistent with the standard of genuine regional herbs. This study introduces an effective technique for swift identification of the primary active compounds in Cortex Fraxini , as well as for an overall assessment of its quality. The combination of spectroscopic techniques and chemometrics provides a rapid and efficient method for the quality analysis of Cortex Fraxini .

研究领域: 药物分析 · 光谱技术 · 化学计量学 · 中药
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JOURNAL OF MATERIALS SCIENCE · 2024 ·Vol. 59 ·期 4 ·1537-1549 · IF 3.5

Ultra-fast response behavior of aluminum hydride (AlH3) in a quasi-detonation environment

Chen Yongjin,Li Yaru,Fu Jianbo,Zhang Mi,Ren Hui,Jiao Qingjie

Aluminum hydride (AlH 3 ), as a potential new metal fuel, has attracted extensive attention in the field of hydrogen storage materials, propellants and energetic materials due to its excellent properties. In this paper, a new organic liquid phase reduction method was used to prepare AlH 3 , and the microstructure and composition of the prepared samples were characterized by SEM–EDS, XRD, FT-IR, XPS, etc. The main crystal phase of the prepared AlH 3 was α-AlH 3 , with high quality and no other impurities. The thermal decomposition behavior and non-isothermal reaction kinetics of AlH 3 were investigated by TG-DSC. The results show that there are three exothermic stages in the heating process of AlH 3 : dehydrogenation of AlH 3 , first oxidation of Al, and second oxidation of Al. The activation energy of the dehydrogenation of AlH 3 is 77.8675 kJ/mol (Kissinger method) and 81.4862 kJ/mol (Ozawa method), respectively. The morphology evolution of AlH 3 particles during the heating process (300–3000 K) was simulated using a reaction kinetics method based on the ReaxFF force field. The response behavior of AlH 3 in the instantaneous high-temperature detonation environment was investigated using the high-energy laser-induced shock wave technique. Under the impact of a high-energy laser (1006 mJ), the AlH 3 sample undergoes an ultra-fast reaction and generates a large amount of plasma. The expansion of the plasma pushes the surrounding air to form a supersonic shock wave and propagates forward. The shock wave propagation velocity of AlH 3 is 690.99 m/s in the range of 2.1–12.35 μs, and the higher the laser energy, the faster the shock wave propagation velocity. This study provides the basis for the application of AlH 3 . Graphical Abstract

CAS / MDL: 108-88-3
研究领域: 氢存储材料 · 推进剂 · 高能材料 · 材料科学 · 化学工程 · 物理学
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POLYMER DEGRADATION AND STABILITY · 2021 · IF 5.03

A pseudo-homogeneous system for PET glycolysis using a colloidal catalyst of graphite carbon nitride in ethylene glycol

Zishuai Wang,Yaoqiang Wang,Shengnan Xu,Yu Jin,Zequn Tang,Gang Xiao,Haijia Su

Glycolysis of poly (ethylene terephthalate) (PET) is a promising way to recycle waste PET and produce bis-(2-hydroxyl ethyl) terephthalate (BHET), the monomer of PET. However, traditional catalysts will cause environment pollution and economic burden. In this work, based on the green and low-cost graphitic carbon nitride colloid, we developed a pseudo-homogeneous system for PET glycolysis, and poly (bisphenol A carbonate) (BPA-PC) and polylactic acid (PLA) methanolysis. Using this system, 100% conversion of PET and 80.30% yield of BHET were achieved, and the reaction time was 2-8 times shorter than that of other metal-based catalysis systems. Catalyst and ethylene glycol were reused five times directly preserving their activity. Furthermore, the degradation of real commercial plastics has also been achieved. According to FT-IR, XPS, and 1 H NMR characterization results, the nucleophilic attack ability of ethylene glycol and electrophilicity of the PET carbonyl's carbon are enhanced by the formation of hydrogen bond between ethylene glycol, PET and catalyst.

CAS / MDL: 959-26-2
研究领域: 材料科学 · 化学工程 · 环境科学 · 催化 · 高分子化学 · 回收技术
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CARBOHYDRATE POLYMERS · 2013 · IF 3.479

Lyophilization as a novel approach for preparation of water resistant HA fiber membranes by crosslinked with EDC

Jie Chen,Cheng Peng,Jun Nie,John F. Kennedy,Guiping Ma

The hyaluronic acid (HA) fibers scaffold with an extracellular matrix mimic structure has been prepared via lyophilization. The morphology of the HA fibers varying the concentration from 0.05   wt% to 0.15   wt% was characterized by scanning electron microscope (SEM). The diameter of HA fibers increased and the morphology changed from fiber to sheet-like structure as the concentration of HA solution increased. To enhance the water-resistance, the pure HA fiber membranes were chemical cross-linked by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC), and confirmed by fourier transform infrared (FT-IR) spectra. In vitro degradation behavior of cross-linked HA fiber membranes in both of water and PBS solutions was investigated, the physical properties were also studied by differential scanning calorimetry (DSC) and thermogravimetry (TG). The results showed that the bonding water capacity increased after crosslinking, and indicated that the crosslinked HA fibers could be used as scaffold in tissue engineering.

CAS / MDL: 25952-53-8
研究领域: 材料科学 · 生物医学工程 · 组织工程
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APPLIED CATALYSIS A-GENERAL · 2021 · IF 5.706

CH2Cl2 catalytic oxidation over Ce-Ti-Zr mixed oxide catalysts

Wei Sun,Shijie Shao,Jun Pan,Yangyang Wang,Hangqi Xia,Xiaohui Gao,Hao Zhang,Qiguang Dai,Li Wang,Xingyi Wang

Ce-Ti-Zr mixed oxide catalysts prepared by sol-gel method were used in catalytic combustion of CH 2 Cl 2 . The characterization reveals that the incorporation of Ce and Zr into TiO 2 anatase or Ti and Zr into CeO 2 fluorite promotes hydroxyl groups, Lewis acidity and surface oxygen through the formation of Ti-O-Zr, Ti-O-Ce and Ce-O-Zr species. Ce-Ti-Zr catalysts show high activity for CH 2 Cl 2 oxidation with the rate of 5.66 × 10 −3 –6.45 × 10 −3 μmol s −1 m −2 at 250 °C and high stability for 50 h. The substitution of surface oxygen for Cl maintains the availability of Ti-OH and thus promotes Cl removal as HCl, which is verified by a great increase in the stable activity of physically closely contacted mixture of separated CeO 2 and TiO 2 or Ti 9 Zr 1 particles. In situ FT-IR shows that CH 2 Cl 2 interacts with Ti-OH to form -O-CH 2 -O-, which is quickly rearranged into formate. Finally, formate is oxidized with surface oxygen into CO or CO 2 .

CAS / MDL: 10294-41-4
研究领域: 催化 · 环境科学 · 材料科学
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Journal of Environmental Chemical Engineering · 2022 · IF 7.968

Preparation of a transition metal-supported TiO2 catalyst and the catalytic oxidative degradation of toluene

Zhengfeng Gu,Daiwei Liu,Mengnan Yu,Teng Bao,Xiaowei Liu,Ling Zhang,Haitao Ding,Zhimin Yu,Chengxun Deng

The synthesis of supported transition metal oxides with satisfactory low-temperature catalytic performance and application potential is still a challenge for the complete degradation of VOCs. Ni-Cu-loaded TiO 2 catalysts were prepared by an impregnation method. The lattice defect and oxygen vacancy concentrations of the prepared materials could be tuned by controlling the Ni/Cu molar ratio and the mass proportion of the TiO 2 support. 5Ni-Cu/TiO 2 exhibited the best catalytic activity and showed superior catalytic stability during complete toluene oxidation . The obtained catalysts were fully characterized by XRD, FT-IR, TEM, N 2 adsorption analysis, XPS, H 2 -TPR, O 2 -TPD, TPD analysis, and XPS. The 5Ni-Cu/TiO 2 catalyst had improved pore sizes and specific surface area, had more oxygen vacancies on its surface, had increased concentrations of adsorbed and lattice oxygen species, and had good redox properties; these characteristics were favorable for low-temperature catalytic performance and catalytic stability. Cyclic transformations of metal valence states between Cu + and Cu and between Ni and Ni 2+ were observed in the catalytic system. A potential catalytic reaction process based on the M-vK mechanism was proposed. This work serves as a reference for the application of supported transition metal catalysts for the degradation of VOCs.

CAS / MDL: 13463-67-7
研究领域: 催化 · 环境科学 · 材料科学
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Polymer Chemistry · 2022 ·Vol. 13 ·期 27 ·4054-4063 · IF 5.364

A facile approach for the preparation of poly(benzothiophene-alt-maleic anhydride) microspheres by self-stabilized precipitation polymerization

Tianxiao Chang,Hongyi Qi,Chenxi Liang,Yanbin Huang,Wantai Yang

Benzothiophene is an under-explored monomer for free radical polymerization. Here we report the preparation of poly(benzothiophene-alt-maleic anhydride) (PBTMA) microspheres with high yield by self-stabilized precipitation polymerization. The chemical structure of the PBTMA copolymer was characterized by 1H-NMR, 13C-NMR, FT-IR and MALDI-TOF MS analyses. The effects of various reaction parameters, including the reaction medium, the monomer concentration, the initiator concentration and the reaction time, on the morphology, particle size and molecular weight (Mn) of the resultant PBTMA microspheres were investigated systematically. The experimental results demonstrated that the PBTMA copolymer was an alternating copolymer, whose composition was independent of the monomer composition. Uniform PBTMA microspheres with the diameter in the range of 400 nm to 3000 nm and Mn up to 12 000 g mol−1 were easily prepared. PBTMA had good solubility in common polar organic solvents and possessed much higher thermal stability than other maleic anhydride copolymers. PBTMA also showed interesting fluorescence properties both in the solid state and in solution. This research has laid the foundation for the further development of PBTMA copolymers as a new material.

CAS / MDL: 108-67-8
研究领域: 高分子科学 · 材料科学 · 化学工程
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2022 · IF 8.025

Amino modified cellulose fibers loaded zinc oxide nanoparticles via paper-making wet-forming for antibacterial materials

Peng Du,Yongjian Xu,Yun Shi,Qinghua Xu,Yang Xu

Bacterial infection has become one of the major threats to human health all over the world, and the development and application of antibacterial materials has drawn great attention. Based on the Schiff-base structure, ZnONPs@ACFs are obtained by loading zinc oxide nanoparticles (ZnONPs) on amino cellulose fibers (ACFs) in-situ through the coordination of amino groups with metal ions. The results of FT-IR, XRD and UV-vis demonstrate that ZnONPs are successfully loaded and uniformly dispersed on ACF surface, and the ACFs maintain intact morphology observed by SEM. Furthermore, the zero-span tensile strength of ZnONPs@ACFs is 66.48 N/cm (ROL: 24.98 N/cm/s) under the optimum conditions, which indicates that ZnONPs@ACFs have a certain strength and can be used to make antibacterial sheet materials via paper-making wet-forming process. Accordingly, the ZnONPs@ACF composites show inhibition zones of 4.95 mm and 1.10 mm against E. coli and S. aureus , respectively. The new cellulose-based antibacterial materials demonstrate potential applications in the field of food packaging and biological medicine etc.

CAS / MDL: 9002-98-6 5970-45-6
研究领域: 材料科学 · 纳米技术 · 生物医学工程 · 化学工程
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Catalysis Science & Technology · 2023 ·Vol. 13 ·期 21 ·6185-6197 · IF 5

Kinetics and optimization studies of modified VPO/γ-Al2O3 catalyst prepared in situ for cross-aldol condensation

Hui Guo,Tingting Ge,Yuchao Li,Yuxia Li,Yanxia Zheng,Xinpeng Guo,Haofei Huang,Ming Wang,Cuncun Zuo

Organic solvent method was used to prepare the active component VPO, which was loaded on ball-milled γ-Al2O3 support. VPO/γ-Al2O3 catalysts were synthesized by in situ generation for the synthesis of acrylic acid (AA) by the aldol condensation of acetic acid (HAc) and formaldehyde (HCHO). The effects of the calcination temperature and the loading of the active component VPO on catalytic activity were systematically investigated. XRD, BET, SEM, CO2/NH3-TPD, FT-IR spectroscopy, and TG techniques were used to characterize the VPO/γ-Al2O3 catalysts. The results showed that the catalyst had the best crystal structure and acid–base activity center at a calcination temperature of 350 °C. The catalytic performance was evaluated using a fixed bed reactor. 60% VPO/γ-Al2O3 exhibited the highest reactivity, and the yield of AA was up to 51.5%. Response surface methodology (RAM) was used to optimize the reaction conditions for aldol condensation. The kinetic equation and reaction order of the aldol condensation reaction were determined using the VPO/γ-Al2O3 catalyst. It provides guidance for the in-depth study of aldol condensation reactions in the future.

研究领域: 催化 · 化学工程 · 材料科学 · 物理化学
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