JOURNAL OF CATALYSIS
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2026
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IF 6
Zhengxi Zou,Zhenke Xu,Weiming Hua,Yinghong Yue,Zi Gao
Catalytic ethane dehydrogenation to ethylene is an attractive route for ethylene production following the shale gas revolution. However, its industrial implementation remains challenging due to high costs and environmental concerns. Iron-based catalysts have been identified as promising alternatives, while their catalytic performance is significantly dependent on the coordination environment and oxidation state of the iron species. Herein, a series of Fe/ZSM-5 catalysts were synthesized via urea precipitation (FeZ-P) and incipient wetness impregnation (FeZ-I) methods to investigate the relationship between Fe species evolution and catalytic behavior during ethane dehydrogenation. The FeZ-P catalysts exhibited significantly enhanced activity compared with FeZ-I, which was attributed to the improved dispersion of iron species and their favorable transformation behavior under reaction conditions. Detailed characterizations of fresh and spent catalysts revealed that the initial Fe 2 O 3 species on FeZ-P surface possessed limited dehydrogenation activity but underwent reaction-induced reduction and carbonization, generating Fe 3 C with enhanced ethane dehydrogenation performance. In contrast, the Fe 2 O 3 bulks on FeZ-I exhibited slower transformation rates, resulting in inferior catalytic activity. Air oxidation treatment enabled partial regeneration of the catalyst by removing carbon deposits and modifying Fe species evolution. This study highlights the importance of regulating Fe species dispersion and dynamic reduction-carbonization behavior, through which catalytically active Fe 3 C can be generated for enhanced ethane dehydrogenation performance. These findings provide valuable insights into the rational design of efficient Fe-based catalysts for non-oxidative alkane dehydrogenation.
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EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
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2019
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IF 4.833
Wen-Lin Tang,Yu Zhang,De-Xuan Hu,Hui Yang,Qian Yu,Jian-Wen Chen,Keli Agama,Yves Pommier,Lin-Kun An
DNA topoisomerase IB (TOP1) regulates DNA topological structure in many cellular metabolic processes and is a validated target for development of antitumor agents. Our previous study revealed that the benzophenanthridone scaffold is a novel chemotype for the discovery of TOP1 inhibitors. In this work, a series of novel 5-aminoethyl substituted benzophenanthridone derivatives have been synthesized and evaluated for TOP1 inhibition and cytotoxicity. Compound 12 exhibits the most potent TOP1 inhibition (+++) and cytotoxicity in human cancer cell lines with GI 50 values at nanomolar concentration range. 12 induces the cellular TOP1cc formation and DNA damage, resulting in HCT116 cell apoptosis . The pharmacokinetics , acute toxicity and antitumor efficiency in vivo of 12 were also studied.
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PubMed
高影响因子
LANGMUIR
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2023
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IF 3.9
Changhao Bing,Xubin Zhang,Fumin Wang,Yi Zhai,Yongwang Li,Kaiwei Wang,Xiaolu Fan,Jinjin Zhang,Qi Shen,Xinyuan He
Zeolite is considered an ideal catalyst for olefin hydration due to its high specific surface area and abundant acid sites. However, the immiscibility of the water–oil two phases in olefin hydration limits mass transfer, and the side reaction of etherification occurs acutely, resulting in a low yield of alcohol. Thus, water–oil amphiphilic HZSM-5 was prepared by sulfonating silanized zeolite. The successful introduction of organic and sulfonic acid groups is demonstrated by FT-IR, TG, and water contact angles. Amphiphilic HZSM-5 can stabilize the Pickering emulsion and catalyze cyclopentene hydration at the phase interface. In addition, NH3-TPD and Py-IR show that the amount of strong Bro̷nsted acid sites of zeolites increases significantly after sulfonation. This facilitates the rate-determining step of cyclopentene activation by H+ to form carbocation. Moreover, the nucleophilic side reactions are inhibited by a high concentration of H+. Finally, under the optimized reaction condition, the conversion of cyclopentene can achieve 5.066% with a selectivity of 85.37% to cyclopentanol, which almost reaches the reaction equilibrium.
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ENVIRONMENTAL TECHNOLOGY
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2023
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IF 2.8
Yuyang Long,Liqun Xiao,Dan Zhou,Yanjun Meng,Lulu Wang,Dongsheng Shen
Chitin biomass is the second largest biomass resource on Earth but under-utilized. In this study, pretreated shrimp shells were converted into value-added platform chemical 5-hydroxymethylfurfural (HMF) using microwave hydrothermal treatment. Under the combined pretreatment of acid decalcification at room temperature and microwave-assisted alkali deacetylation, the HMF yield could reach 1.8 wt%. The key process parameters, including the holding temperature, holding time, and pH value, were evaluated and optimised. The highest HMF yield of 6.5 wt% was obtained at 202.6°C at a holding time of 5.8 min and a pH value of 1.5. This result demonstrates the potential of synchronously treating waste and recycling it, thereby offering a highly promising valorisation strategy for chitin-biomass utilisation.
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CHEMICAL ENGINEERING JOURNAL
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2023
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IF 15.1
Zhenfei Yang,Xinnian Xia,Ming Fang,Longlu Wang,Yutang Liu
The selective oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-dicarbofuran (DFF), and 2,5-furanedicarboxylic acid (FDCA) is essential to its practical application. Herein, a novel Pt/ZIS/MnO 2 (PMZIS) photocatalysts with photothermal effect were well designed for selective and controlled oxidation of HMF toward DFF or FDCA. The product distribution of HMF photo-oxidation on PMZIS can be regulated by the photothermal effect. At a low temperature (10 °C) with PMZIS, DFF is the primary oxidation product with the yield of 54.6% and selectivity of 85.4%. At a high temperature (60–70 °C) induced by photothermal effect, the FDCA can be obtained with the yield of 61.5 % and selectivity of 82.9%. Moreover, the Z-scheme transfer pathway and Pt cocatalysts realize the spatial charge separation structure of PMZIS heterojunctions. This unique structure greatly inhibits charge recombination and maximizes the activation ability of molecular oxygen to efficiently generate of the reactive oxygen species (e.g., 1O 2 and O 2– ), thus significantly improving the photocatalytic performance. This work would provide valuable insight in the product regulation through photothermal effect for the photocatalytic specific selective oxidation of organic molecules.
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MATERIALS LETTERS
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2023
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IF 3
Yuanyuan Tao,Wenhui Wei,Qianqian Gu,Xiaoping Jiang,Dongwei Li
The desilicated zeolite ZSM-5 (des-ZSM-5) based composite polymer electrolytes (CPEs) PZEw was fabricated via phase inversion processes and in-situ polymerization with polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP) and liquid electrolyte 1 M lithium bis(trifluoromethanesulphonyl)imide (LiTFSI) in vinylene carbonate (VC) (VC@LiTFSI). Assisted by des-ZSM-5, PZEw possess excellent thermal stability, mechanical properties, high ionic conductivity (2.75 × 10 −4 S cm −1 , 25 °C), and enlarged electrochemical windows (4.94 v, vs. Li + /Li). Meanwhile lithium metal batteries (LMBs) LiFePO 4 (LFP)/PZEw/Li showed superior rate performance and long-time cycling stability.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2023
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IF 4.2
Lu Lu,Xinlei Ji,Xuewei Wang,Fangming Jin,Xi Chen
5-Hydroxymethylfurfural (5-HMF) is one of the top valuable platform chemicals that can be derived from biomass. Herein, a facile, mild, and efficient catalytic conversion method was developed to convert chitin biomass into 5-HMF in lithium bromide molten salt hydrates (LiBr MSHs) with boric acid (BA) as the catalyst. About 49.6% 5-HMF yield was obtained from glucosamine (GlcN) in 65 wt % LiBr MSHs at 130 °C for 2 h with 800% BA addition. The system is applicable to other sugars, and the C2-substituted group of sugars played a significant role in the 5-HMF yield. The 5-HMF yields were 81.3, 40.3, and 3.9% from fructose, glucose, and N-acetyl glucosamine (GlcNAc), respectively, under identical conditions. Combined with acid addition and Box–Behnken experiment designs, the direct conversion of chitosan and chitin were achieved at 140 °C for 5 h to produce 5-HMF with 21.6 and 15.3% yield. Ammonia quantitative analysis and NMR tests have been conducted, based on which a plausible reaction pathway was proposed. The LiBr MSHs and the BA catalyst facilitated the hydrolysis, deacetylation, and ring-opening of chitin biomass. Especially, the catalyst BA played a key role in the formation of 5-HMF, as it was found to promote dehydration at the last step. The study put forward new avenues for chitin refinery to produce high-value furanic platform chemicals in cheap and green solvent systems.
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Molecular Catalysis
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2023
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IF 4.6
Quan Zhang,Wei Huang,Wenhao Cui,Xingzong Dong,Guangye Liu,Yunpeng Xu,Zhongmin Liu
The acidity and porosity of zeolite catalysts are crucial parameters affecting the catalytic performance. In this work, alkali treatment and metal species loading were used to modify the porosity and acidity of ZSM-5 zeolite to prepare an efficient catalyst for the 1,2-dichloroethane cracking reaction. After optimization, the highly active catalyst Zn (1%) /ZSM-5-120 was obtained, and 78% conversion of EDC and 99% selectivity toward VCM could be achieved under the conditions of 300 °C and 3.0 h −1 (WHSV). A detailed investigation was conducted on the effects of acidity, texture properties and metal species loaded on ZSM-5 zeolite on the 1,2-dichloroethane cracking reaction.
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ACS Applied Materials & Interfaces
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2023
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IF 9.5
Wenlei Gu,An Pei,Shiyi Zhang,Feifei Jiang,Yanyan Jia,Qizhen Qin,Ruian Du,Zhengjian Li,Renfeng Liu,Yongcai Qiu,Keyou Yan,Yun Zhao,Cheng Liang,Guangxu Chen
The development of single-atom catalysts with effective interfaces for biomass conversion is a promising but challenging research area. In this study, a Ru1/CoOx catalyst was successfully fabricated with the impregnation method, which featured Ru single atoms on a cobalt oxide substrate. The Ru1/CoOx catalyst showed superior performance in the selective electrooxidation of 5-hydroxymethylfurfural (HMF) to produce 2,5-furandicarboxylic acid (FDCA), a high value-added product. The introduction of Ru single atoms with an ultralow loading of ∼0.5 wt % was revealed to accelerate the electroredox of Co2+/Co3+/Co4+ and improve the intrinsic activity of the CoOx substrate with an FDCA selectivity of 76.5%, which is better than that of the pristine CoOx electrocatalysts (62.7%). The interfacial synergistic effect of the Ru1/CoOx interface clarified that Ru single atoms can enhance the adsorption of HMF at the Ru1/CoOx interface, which promoted the rate-determining step of the selective C–H bond activation for FDCA production. This finding provides valuable insights into the rational design of single-atom catalysts with functional interfaces for biomass upgrading.
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CHEMICAL ENGINEERING JOURNAL
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2023
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IF 15.1
Qiang Sun,Hongxia Gao,Teerawat Sema,Zhiwu Liang
High energy consumption during the carbon dioxide (CO 2 ) desorption process in amine-based CO 2 capture technology is a crucial hindrance to achieving carbon neutrality. HZSM-5 is one of the most widely reported solid acid catalysts used in primary amine regeneration. This work compared a series of HZSM-5 zeolites with different Si/Al ratios in terms of CO 2 desorption performance. To further enhance catalytic activity, hierarchical HZSM-5 was synthesized by the dealumination and desilication re-assembly method with different acid and alkali concentrations. The experimental results suggested that desilication by modification in sodium hydroxide resulted in a significant improvement of mesoporous surface area. The NaOH-0.4 catalyst could improve the amount of desorbed CO 2 by 40.3% and decrease the relative heat duty by 28.5%. And the cyclic tests revealed that catalytic activity was well preserved in the recycling process. Moreover, the structure and acidity of modification samples were characterized by X-Ray diffraction (XRD), Fourier transforms infrared (FT-IR), Nitrogen adsorption–desorption experiment, temperature programmed desorption of ammonia (NH 3 -TPD), Pyridine-adsorption infrared spectroscopy (Py-IR), and scanning electron microscopy (SEM). The characterization results suggested that the synergistic effect of larger mesoporous surface area and total acid sites was important to enhance catalytic CO 2 desorption performance. These results showed a new understanding of catalyst design for CO 2 capture technology by modifying the structure of the catalyst support.
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CHINESE JOURNAL OF CATALYSIS
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2023
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IF 16.5
Hongfang Wang,Leitao Xu,Jingcheng Wu,Peng Zhou,Shasha Tao,Yuxuan Lu,Xianwen Wu,Shuangyin Wang,Yuqin Zou
5-Hydroxymethylfurfural (HMF) electrooxidation in neutral conditions is a promising strategy to suppress the formation of humins and corrosive effects on electrochemical devices. However, scarce studies have been reported in neutral media due to the deficiency in electrophilic oxygen (eg OH – ) required for the activation of HMF. Herein, 2,2,6,6-tetramethyl-piperidine-1-oxyl (TEMPO)/Co 3 O 4 was utilized to co-catalyze HMF in neutral media, successfully achieving 2,5-furandicarboxylic acid (FDCA) with yield > 99%. It was found that TEMPO could promote HMF dehydrogenation to 2,5-diformylfuran (DFF) and simultaneously activated water via hydrogen-bonding interactions. As a result, the formation of OH* in neutral electrolytes was favored, which was absorbed by electrogenerated active Co species to facilitate subsequent conversion of formyl-group-involved intermediates to FDCA. This work provides a current understanding of the catalytic mechanism for HMFOR in neutral media and guides the design of highly efficient electrocatalysts for biomass upgrading.
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JOURNAL OF SOLID STATE CHEMISTRY
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2019
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IF 2.291
Luyu Wang,Yunling Wu,Junkuo Gao,Jia Song
Solid AlPO-5 and La doped AlPO-5 (La/AlPO-5) were synthesized by a hydrothermal treatment followed by crystallization and calcination . The ammonia (NH 3 ) sensing properties of AlPO-5 and La/AlPO-5 were evaluated by using quartz crystal microbalance (QCM) platform to work out the enhanced effect of La doping treatment. La/AlPO-5 possessed a higher response to NH 3 than that of AlPO-5 with same concentration. In addition to the favorable sensitivity, La/AlPO-5 based sensor also showed prominent repeatability and selectivity. We also explored the thermodynamics and humidity-enhanced effect in the NH 3 sensing process.
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危险品化学品经营许可证（带存储）