APPLIED CATALYSIS A-GENERAL
·
2024
·
IF 4.7
Chenyang Zhao,Yujia Liu,Yupeng Tian,Yahui Li,Junjie Feng,Wei Xu,Ning Shi,Zhe Yang,Bing Sun
Direct epoxidation of propylene (C 3 H 6 ) with hydrogen (H 2 ) and oxygen (O 2 ) over Au/TS-1 catalyst was promising way for the synthesis of propylene oxide (PO). However, high selectivity of PO (>95 %) and conversion of C 3 H 6 (>5 %) cannot be achieved at the same time. The industrialization process was severely restricted. In this paper, Au/TS-1 catalysts were synthesized by deposition precipitation method with alkali metal promoter. And alkaline gases and silane coupling post-treatment were performed to promote the catalytic activity. The prepared samples exhibited a much better C 3 H 6 conversion (6.5 %) and PO selectivity (95.1 %) compared with general catalyst using normal synthetic technology. Cs 2 CO 3 was beneficial to increasing Au nanoparticles uptake efficiency. Both NH 3 and triethoxyvinylsilane post-treatment were good for smaller and more uniform loading of Au nanoparticles. The decreasing in surface hydroxyl density effectively alleviated the occurrence of PO ring opening isomerization. The increased hydrophobicity of TS-1 surface was conducive to the rapid desorption of generated PO and significantly increased PO selectivity. Multiple pretreatment was also favorable for extending the lifetime of Au/TS-1 catalyst.
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2024
·
IF 4.1
Haoqing Tang,Yulan Wang,Xiaohuan Liu,Tian Tian,Qiang Weng,Xiaotong Liu,Tao Liu
Rational design and preparation of titanium-based anode materials with superior fast charge and discharge are a key focuses of the lithium-ion batteries research. Herein, a novel and facile synthesis of uniformly carbon-coated Li 2 CuTi 3 O 8 (LCuTO) nanoparticles with excellent high-rate lithium storage properties is presented using HKUST-1 with pore structure and active metal sites as a copper source. The well-designed LCuTO@HKUST with carbon bridges between the particles and the carbon layer on the outer surface offers high electronic conductivity for fast charge and discharge. The LCuTO@HKUST exhibits extraordinary lithium storage performance: high capacity (251.8 mAh/g after 1000 cycles at a current density of 1.0 A/g), a superior high-rate capability (160.3 mAh/g after 500 cycles at 3.0 A/g and 138.1 mAh/g after 500 cycles at 5.0 A/g), and excellent cycle reversibility and cycle stability under various current densities. In addition, the lower Li + migration barrier in LCuTO@HKUST demonstrated by density functional theory (DFT) calculations is beneficial to the long-cycle stability and high-rate performance. The proposed preparation method and the strategy of using the MOF as a metal source for lithium-ion battery anode materials provide a new approach for advanced fast charge–discharge energy storage applications.
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Molecular Catalysis
·
2021
·
IF 5.062
Jiarong Li,Zhe Liu,Guangfa Hu,Ruimin Gao,Ronglan Zhang,Jianshe Zhao
A series of hybrid catalyst PMoW@HKUST-1@ZSM-5-MCM-41 was prepared in which H 3 PMo 6 W 6 O 40 were supported in the pore of micro/mesoporous materials ZSM-5-MCM-41 and HKUST-1 by one-pot method. Five types of ZSM-5-MCM-41 were prepared and corresponding ODS catalysts PMOW@HKUST-1@ZSM-5-MCM-41 were synthesized. The prepared catalysts were characterized and the most efficient catalyst was selected by XRD, FT-IR, UV–vis, N 2 adsorption-desorption, SEM, TEM. The removal of DBT reached 98.13 % by using PMoW@HKUST-1@ZSM-5-MCM-41−2 under 60 °C with molecular oxygen as oxidant after 150 min. After desulfurization, the catalyst can be simply recovered and reused 7 times with an unnoticeable decrease in catalytic activity, indicating the successful combination of heteropolyacids and micro/mesoporous materials for desulfurization.
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CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Shijie Yao,Yaru Hu,Jianfeng Ye,Jianhao Xie,Xuetao Zhao,Lingli Liu,Shuguang Lyu,Kuangfei Lin,Changzheng Cui
The super-resistant bacteria that produce the New Delhi metallo-β-lactamase 1 (NDM-1) enzyme are becoming a conceivably major worldwide clinical issue with serious consequences. Studying the disinfection and mechanism of super-resistant bacteria and their antibiotic resistance genes (ARGs) is crucial for controlling their spread in the water environment. In this study, the disinfection of the super-resistant bacterium Acinetobacter sp. CS-2 and its transferable ARGs (plasmid-encoded bla NDM-1 and bla OXA-58 ) by ultraviolet radiation (UV), peroxymonosulfate (PMS), and ultraviolet/peroxymonosulfate (UV/PMS) exposure were investigated. UV/PMS could completely inactivate CS-2 and control the photoreactivation risk, while bacteria that underwent UV and PMS treatment had survival ratios of 0.22% and 0.28%, respectively. The removal efficiencies of bla NDM-1 and bla OXA-58 ranged from 3.64 to 4.05 log, and the advantage of UV/PMS treatment on ARGs damage was further identified by gel electrophoresis analysis. The removal efficiency of bla NDM-1 was lower than that of bla OXA-58 , which was attributed to the low number of adjacent 5′-TT-3′ harbored by bla NDM-1 . The removal rate constants of the ARGs by UV treatment were significantly correlated with the number of adjacent base pairs (e.g., 5′-TT-3′, 5′-CT-3′, 5′-TC-3′ and 5′-CC-3′) and length, with R -values ranging from 0.9044 to 0.9512. Singlet oxygen ( 1 O 2 ) played a vital role in the reduction of bla NDM-1 and bla OXA-58 in the UV/PMS treatment. UV/PMS showed high removal efficiency under natural pH conditions and in the presence of various aqueous ions (e.g., Cl − , SO 4 2− and HCO 3 − ). Overall, this study provides new understandings and theoretical support for the risk control of super-resistant bacteria and plasmid-encoded ARGs.
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MICROPOROUS AND MESOPOROUS MATERIALS
·
2022
·
IF 5.876
Mingming Hu,Junjie Liu,Jingjing Kong,Peiyu Jia,Ning Qi,Yichu Wu,Zhiquan Chen,Shan Xu,Nanwen Li
In this work, a series of hydrolyzed polymers of intrinsic microporosity (PIMs) membranes were successfully synthesized under alkaline conditions. Positron annihilation lifetime measurement is employed to analyze the pore structure of the hydrolyzed PIMs. In the original PIM-1, there are two kinds of pores, i.e. micropores with radius of 4.32 Å and ultramicropores with radius of 2.58 Å. The size of all the pores shows a continuous decrease with increasing hydrolysis time, which is confirmed by the reduced chain-to-chain spacing in the hydrolyzed PIMs measured by X-ray diffraction. Meanwhile, the fractional free volume also shows decrease after the hydrolysis process, while the relative number of ultramicropores increases. Benefiting from the smaller pore size in the hydrolyzed PIMs membrane, the gas molecules with smaller size (such as CO 2 ) can be separated more efficiently. The selectivity of CO 2 /CH 4 of hydrolyzed PIMs reaches up to 30.05 with a relatively high CO 2 permeability of 140.58 Barrer, which exceeds the Robeson’s 1991 upper bound. Our results indicate that the hydrolyzed polymers of intrinsic microporosity membranes are promising candidates for gas separation membrane in the future.
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MOLECULES
·
2024
·Vol. 29
·期 18
·4375
·
IF 4.2
Ran Luo,Haoyi Zhao,Siqi Deng,Jiale Wu,Haijun Wang,Xiaoshan Guo,Cuicui Han,Wenkang Ren,Yinglong Han,Jianwen Zhou,Yu Lin,Ming Bu
In this study, novel ergosterol peroxide (EP) derivatives were synthesized and evaluated to assess their antiproliferative activity against four human cancer cell lines (A549, HepG2, MCF-7, and MDA-MB-231). Compound3gexhibited the most potent antiproliferative activity, with an IC50value of 3.20 µM against MDA-MB-231. This value was 5.4-fold higher than that of the parental EP. Bioassay optimization further identified3gas a novel glutaminase 1 (GLS1) inhibitor (IC50= 3.77 µM). In MDA-MB-231 cells,3greduced the cellular glutamate levels by blocking the glutamine hydrolysis pathway, which triggered reactive oxygen species production and induced caspase-dependent apoptosis. Molecular docking indicated that3ginteracts with the reaction site of the variable binding pocket by forming multiple interactions with GLS1. In a mouse model of breast cancer,3gshowed remarkable therapeutic effects at a dose of 50 mg/kg, with no apparent toxicity. Based on these results,3gcould be further evaluated as a novel GLS1 inhibitor for triple-negative breast cancer (TNBC) therapy.
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PubMed
高影响因子
ENVIRONMENTAL POLLUTION
·
2019
·
IF 5.714
Yi Shen,Chao Zhu,Baoliang Chen
To improve catalytic performance and stability of Ag nanoparticles (Ag NPs), a facile ultrasonication-assisted chemical reduction method was developed to fabricate reduced graphene oxide (rGO) aerogels loaded with 1–3 nm Ag NPs under the normal temperature and pressure. The ultrasonication facilitated the dispersion of Ag(I) in the form of silver ammonia and anchored onto GO nanosheets . Ag(I) and GO were simultaneously reduced to Ag(0) immobilizing onto 3D rGO hydrogels within the heterogeneous liquid phase, and ultimately formed 3D rGO-Ag NPs aerogels . The 3D rGO-Ag NPs aerogels displayed superb catalytic performance for the reduction of nitrobenzene (NB), 1,3-dinitrobenzene (DNB) and 4-nitrophenol (NP) into aniline, 1,3-diaminobenzene and 4-aminophenol, respectively. The individual reduction rate K obs for NB, DNB and NP were 0.168 h −1 , 0.109 h −1 and 0.092 h −1 , which were much higher than those of other Ag NPs-based materials. Moreover, the immobilization of 1–3 nm Ag NPs in 3D rGO-Ag NPs was stable during the whole reduction reaction without aggregation and leaching. The high stability of Ag NPs in 3D rGO-Ag NPs and superb performance on catalytic reduction of nitroaromatic compounds (NACs) could be concluded into ultrasonication influence in the preparation procedure and synergistic effect of Ag NPs and 3D rGO in the catalytic reduction process. The simple ultrasonication-assisted chemical reduction approach provided a scaled-up application prospect in catalytic reduction of NACs by metal nanoparticle catalysts.
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MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING
·
2021
·
IF 3.927
Yihang Dong,Xiangnan Wang,Ye Han,Shuyu Yao
{(ZrO 2 ) 0.92 (Y 2 O 3 ) 0.08 } 1- x (CuO) x (ZYC) synthesized by the co-precipitation method with different stoichiometry ( x =0, 0.1, 0.2 and 0.3) are evaluated through thermogravimetric-differential scanning calorimetry (TG-DSC), X-ray diffraction (XRD) and electrical conductivity using an electrochemical workstation and the effects of CuO doping content on the above properties are researched, respectively. The results are discussed in terms of the potential as diffusion barrier material to be applied in diffusion barrier limiting current oxygen sensors application at temperatures from 500 to 850 °C. Results derived from TG-DSC shows that the weight loss of the sample is mainly due to the decomposition of the precursor, forming ZYC above ~600 °C. XRD analysis shows that the ZYC sample is a cubic phase and the CuO doping is benefit to the crystallinity of ZYC. The electrical conductivity results indicate that the total conductivity decreases for ZYC1 but then increases with the increase of CuO doping content and reaches the maximum total conductivity of 2.02 × 10 −1 S cm −1 at 850 °C and the activation energy ( E a ) is 0.93 eV for ZYC3.
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GENERAL PHYSIOLOGY AND BIOPHYSICS
·
2024
·Vol. 43
·期 1
·13-23
·
IF 1.3
Xiao Jin,Ling Jin,Bingxin Wu,Danping Xu
Myocardial ischemia/reperfusion (I/R) causes serious threats to human life. Naringenin, a polyphenolic compound naturally occurring in citrus fruit, has cardioprotective effects against myocardial I/R injury. Besides, miR-24-3p is also reported to have cardioprotective effects. We intended to explore whether the cardioprotective effects of naringenin relate to miR-24-3p and its underlying mechanism. In this study, we used an in vivo rat myocardial I/R model and an in vitro cardiomyocyte H9c2 hypoxia/reoxygenation (H/R) model. Myocardial injury was detected by hematoxylin-eosin staining and ELISA for creatine kinase (CK), malondialdehyde (MDA), and lactate dehydrogenase (LDH). miR-24-3p and cell death inducing p53 target 1 (Cdip1) mRNA expressions were examined by RT-PCR. We find that naringenin pretreatment significantly relieves myocardial I/R injury, reduces LDH, CD, and MDA levels, and increases miR-24-3p expression. Furthermore, miR-24-3p alleviates myocardial I/R injury partially through regulating Cdip1. Moreover, naringenin protects myocardial I/R injury partially by regulating miR-24-3p to inhibit Cdip1 expression. In conclusion, our data suggest naringenin protects myocardial I/R injury partially through miR-24-3p/Cdip1 axis.
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PubMed
高影响因子
JOURNAL OF POLYMER RESEARCH
·
2013
·Vol. 20
·期 7
·1-9
·
IF 2.019
Xu Jingmei,Ren Chunli,Cheng Hailong,Ma Li,Wang Zhe
Double fluoride 2,5-bis(4-fluorophenyl)-1,3,4-oxadiazole (BFO) monomer was synthesized. Copolymerization of BFO, 2,2-bis(4-hydroxypheny)propane (bisphenol A) and 3′3-disulfonate-4′4-dichloro dipheny sulfone (SDCDPS) at different molar ratio resulted in a new poly (aryl ether sulfone) containing 1, 3, 4-oxadiazole polymers (SPAESO). The structures of monomer BFO and copolymer were confirmed by FT-IR and 1 H NMR. The TEM pictures showed that the ion clusters were formed and distributed evenly in SPAESO copolymer matrix. The sulfonated polyoxadiazole membranes exhibited excellent thermal, dimensional and oxidative stability and lower methanol diffusion coefficient. The proton conductivity of SPAESO-3 was 7.5 × 10 −2 Scm −1 at 120 °C while the methanol permeability coefficient of SPAESO-3 was only 2.23 × 10 −7 cm 2 S −1 at 25 °C. According to the comprehensive performance, the sulfonated polyoxadiazole membranes may be the alternative materials as proton exchange membrane for PEMFC at medium-high temperature operation.
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BIOELECTROCHEMISTRY
·
2022
·
IF 5.76
Xianghui Li,Yichan Huang,Jiawen Chen,Shuangmu Zhuo,Zhenyu Lin,Jianxin Chen
A sensitive homogeneous electrochemiluminescence (ECL) biosensor for flap endonuclease 1 (FEN1) detection was developed by combining highly sensitive ECL detection, high efficiency of branched hybridization chain reaction (BHCR) amplification, a convenient homogeneous strategy, and simple ultrafiltration separation. Magnetic beads were first modified with well-designed double flap DNAs containing 5′-flaps. In the presence of FEN1, the 5′-flap can be cleaved, and a large amount of single-stranded DNA can be produced, which can be separated easily from the double-flap DNA-modified beads by a magnet. Then, the cleaved 5′-flap can be used to initiate BHCR amplification to produce a large amount of long-strand dsDNA. Ru(phen) 3 2+ can insert dsDNA to form Ru-dsDNAs, which can be easily separated from the main solution through ultrafiltration. The ECL signal from the separated Ru-dsDNAs has a good linear relationship with the logarithm of the FEN1 concentration ranging from 6.5 × 10 −2 ∼ 6.5 × 10 3 U/L with a detection limit of 2.2 × 10 −2 U/L. The proposed biosensor was used to evaluate FEN1 activity in real samples with satisfactory results.
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MACROMOLECULAR RAPID COMMUNICATIONS
·
2022
·Vol. 44
·期 6
·2200826
·
IF 5.006
Jiaqi Li,Weilin Feng,Mengxiao Zhang,Xiaohe Wang,Chuanjie Fang,Jianyu Wang,Lin Zhang,Liping Zhu
Polymers of intrinsic microporosity (PIMs) are a class of microporous organic materials that contain interconnected pores of less than 2 nm in diameter. Such materials are of great potential used in membranes for molecular separation, such as drug fractionation in pharmaceutical industry. However, the PIMs membranes are often susceptible to low separation selectivity toward different molecules due to their wide pore size distribution. Herein, a linear polyimide, Matrimid, is incorporated with PIM-1 (a typical member of PIMs) by solution blending, and the blends are dip-coated onto a polyimide P84 support membrane to prepare thin-film composite (TFC) membranes to control pore size distribution while keep high microporosity. The component miscibility, pore characteristics, and molecular separation performances of the Matrimid/PIM-1 TFC membranes are investigated in detail. The Matrimid and PIM-1 are partially miscible due to their similar Hansen solubility parameters. The Matrimid endows the selective layers (coatings) with narrower pore size distribution due to more compact chain packing. The prepared Matrimid/PIM-1 TFC membranes show high selectivity for separation of riboflavin (80% of retention) and isatin (only 5% of retention). The developed membranes exhibit great potential for separating molecules with different molecular weights.
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