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Journal of Energy Storage · 2022 · IF 8.907

Experimental design of 1-dodecanol@methylated melamine-formaldehyde microencapsulated composite phase change material and the application in energy storage field

Dengji Xu,Wanyu Shen,Shiqi Sun,Yanjun Chen,Zhumao Lu,Xiaokai Meng,Chao Wang,Li Guo,Changcheng Liu,Que Huang

The purpose of this study is to explore a new clean and environment protecting composite microcapsule material with 1-dodecanol (DD) as the core and modified methylated melamine-formaldehyde (MMF) as the shell, to meet the needs of low temperature heat or energy storage (0–40 °C). The microencapsulated phase change material (MPCM) base with a mass ratio of 14:3 was synthesized by in-situ emulsion polymerization , then two kinds of additives 10 wt% boron nitride (BN) and 5 wt% BN mixed with 5 wt% carbon nanotubes (CNTs) were applied to solve the defects of easy leakage and low thermal conductivity , while the samples were defined and shorted as BPCM and BCPCM, respectively. The experimental results showed that the prepared BCPCM presented good storage stability in the temperature range of 0–40 °C, which was due to its good thermal conductivity of 0.584 W/m·K, latent heat of 163.8 J/g, and strong supramolecular interaction between 1-DD and MMF. Through charging and discharging tests for batteries under low temperature, BCPCM indicated excellent thermal management performance, which proposed its application potential in the cryogenic storage environments and battery thermal management system (BTMS) field.

✓ 已验证 DOI 高影响因子
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IONICS · 2021 ·Vol. 27 ·期 9 ·3761-3768 · IF 2.817

A composite cathode material for lithium-ion batteries: synthesis and electrochemical properties of xNa3V2(PO4)2F3·(1-x)Na2MnPO4F@C

Li Wei,Ai Huiting,Liu Zheng,Wei Chuchu,Han Guo-Cheng,Zhan Ling

In order to improve the electrochemical properties of Na 2 MnPO 4 F (NMPF), low-cost biomass cane bagasse was used as a carbon source for coating, Na 3 V 2 (PO 4 ) 2 F 3 (NVPF) was used as a doped phase to prepare different ratios of xNa 3 V 2 (PO 4 ) 2 F 3 ·(1-x)Na 2 MnPO 4 F@C (NVPF/NMPF@C) composite materials via a sol–gel method. The results including analysis of XRD, SEM, EDS, and XPS methods showed that NVPF/NMPF@C (x = 0.2) composite material had good crystallinity, and NVPF can be uniformly doped in NMPF@C. The rate performance of NVPF/NMPF@C composite was tested at 0.1, 0.2, 0.5, 1, and 2 C. The first discharge specific capacity of NVPF/NMPF@C composite electrode material reached 193 mAh/g and increased by approximately 20 times when compared to only 9 mAh/g of NMPF@C. The coulombic efficiency of NVPF/NMPF@C material remained 95% after 35 cycles at 0.1 C. The introduction of NVPF can improve charge transfer and Li + diffusion, and enhance the electrochemical behavior of the lithium-ion battery cathodes.

✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Disinfection and mechanism of super-resistant Acinetobacter sp. and the plasmid-encoded antibiotic resistance gene blaNDM-1 by UV/peroxymonosulfate

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.

✓ 已验证 DOI 高影响因子
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ENVIRONMENTAL POLLUTION · 2019 · IF 5.714

Immobilizing 1–3 nm Ag nanoparticles in reduced graphene oxide aerogel as a high-effective catalyst for reduction of nitroaromatic compounds

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.

✓ 已验证 DOI 高影响因子
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MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING · 2021 · IF 3.927

Crystal structure and electrical conductivity of {(ZrO2)0.92(Y2O3)0.08}1-x(CuO)x (x=0, 0.1, 0.2 and 0.3)

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.

✓ 已验证 DOI 高影响因子
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MOLECULES · 2024 ·Vol. 29 ·期 18 ·4375 · IF 4.2

Discovery and Optimization of Ergosterol Peroxide Derivatives as Novel Glutaminase 1 Inhibitors for the Treatment of Triple-Negative Breast Cancer

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.

✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2024 · IF 4.1

Ultrahigh rate and cycling properties of Li2CuTi3O8 anode derived from HKUST-1 copper source for high-performance lithium-ion batteries

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.

✓ 已验证 DOI 高影响因子
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APPLIED CATALYSIS A-GENERAL · 2024 · IF 4.7

Enhanced catalytic performance for gas phase epoxidation of propylene with H2 and O2 by multiple pretreated Au/TS-1 catalysts

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.

✓ 已验证 DOI 高影响因子
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MICROPOROUS AND MESOPOROUS MATERIALS · 2022 · IF 5.876

Free volume and gas transport properties of hydrolyzed polymer of intrinsic microporosity (PIM-1) membrane studied by positron annihilation spectroscopy

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.

✓ 已验证 DOI 高影响因子
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Molecular Catalysis · 2021 · IF 5.062

Heteropolyacids supported on micro/mesoporous materials PMoW@HKUST-1@ZSM-5-MCM-41: Effective catalyst for oxidative desulfurization with oxygen

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.

✓ 已验证 DOI 高影响因子
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GENERAL PHYSIOLOGY AND BIOPHYSICS · 2024 ·Vol. 43 ·期 1 ·13-23 · IF 1.3

Naringenin protects myocardial ischemia/reperfusion injury by regulating miR-24-3p to inhibit cell death-inducing p53 target 1 expression

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.

✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF POLYMER RESEARCH · 2013 ·Vol. 20 ·期 7 ·1-9 · IF 2.019

Sulfonated poly (aryl ether sulfone) containing 1, 3, 4-oxadiazole as proton exchange membranes for medium-high temperature fuel cells

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.

✓ 已验证 DOI 高影响因子
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