JOURNAL OF ELASTOMERS AND PLASTICS
·
2023
·
IF 1.7
Xiaoyong Yang,Xiaofang He,Fuqin Xu,Zhaoyang Hou,Zhihui Ma,Jing Cai,Ruimin Jiao
With the rapid development of electronic devices and rubber tires, the industry has put forward new requirements for the heat dissipation of rubber components. With excellent thermal conductivity, oxidation resistance, and thermal stability, hexagonal boron nitride (h-BN) is often added to plastics or rubber as a thermally conductive filler, but is less effective when used directly. In this study, h-BN-K was prepared by direct modification of the mixed solution of KH-550, and KH-570, while h-BN-PK was prepared by co-modification of dopamine, KH-550, and KH-570. Two modified h-BN were added to natural rubber (NR) to improve the vulcanization properties, mechanical properties, and thermal conductivity. It was found that the tensile strength and thermal conductivity of 20 wt% h-BN-PK/NR composites were 30.6 MPa and 0.335 W/mK, which were 39.1% and 110.7% higher compared to pure NR (22.0 MPa and 0.159 W/mK), respectively. In addition, the addition of h-BN improved the thermal stability performance of NR to some extent. In conclusion, the h-BN-PK/NR composites provide a certain reference for the use of thermally conductive NR and suggest new ideas for heat dissipation of electronic devices.
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高影响因子
FUEL
·
2025
·
IF 7.5
Yali Niu,Rui Yao,Shuhui Fan,Jinping Li,Guang Liu
Anion-exchange membrane water electrolyzers (AEMWE) are promising for clean hydrogen production. However, the high energy barriers associated with water adsorption and dissociation combined with the high adsorption energy of hydrogen intermediates (H*) in alkaline environment result in slow kinetics for the hydrogen evolution reaction (HER). To tackle this, we report a catalyst comprising Pt nanoparticles loaded on Co(OH) 2 /PTI nanosheets (Pt/Co(OH) 2 /PTI) for efficient alkaline HER at high current densities. Operando characterization indicates that Co(OH) 2 promotes H 2 O adsorption and dissociation, while the Pt nanoparticles optimize H* adsorption energy, enabling preferential H* adsorption at the Pt site to facilitate H 2 generation and desorption. Furthermore, the ultra-thin poly (triazine imide) (PTI) support prevents the Pt nanoparticles aggregation, thereby enhancing catalyst stability. As a result, the synergistic Pt/Co(OH) 2 /PTI achieves superior HER performance, demanding an overpotential of merely 7 mV to achieve a current density of 10 mA cm −2 and just 220 mV to drive 1 A cm −2 , and it maintains stable for over 220 h under the condition of 1 A cm −2 . Additionally, the electrolyzer assembled using Pt/Co(OH) 2 /PTI as the cathode demonstrates stable operation for 200 h at 0.5 A cm −2 under 70 °C, highlighting its strong potential for industrial applications.
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高影响因子
Catalysts
·
2019
·Vol. 9
·期 10
·869
·
IF 3.444
Xinyu Liu,Meihuan Lu,Xuan Wang,Juyou Lu,Jianxin Yang
For decades the steric effect was still ambiguously understood in catalytic benzylation reactions of arenes with benzyl alcohol, which limited the green synthesis of phenylmethane derivates in industrial scale. This research applies a series of silica–alumina beta zeolites to systematically evaluate factors like catalyst porosity, reactants molecule size, and reaction temperature on catalytic benzylation. First, a suitable hierarchical beta zeolite catalyst was screened out by X-ray powder diffraction, N2adsorption−desorption, and probe benzylation withp-xylene. In the following substrates expanding study, for a typical benzylation of benzene, it showed extraordinary performance among literature reported ones that the conversion was 98% while selectivity was 90% at 353 K only after 10 min. The steric effect of aromatics with different molecular sizes on benzylation was observed. The reaction activities of four different aromatics followed the order: benzene > toluene >p-xylene > mesitylene. Combined with macroscopic kinetic analysis, this comprehensive study points out for the first time that the nature of this steric effect was dominated by the relative adsorption efficiency of different guest aromatic molecules on the host zeolite surface.Keywords:benzylation;benzyl alcohol;hierarchical zeolite;steric effect;green catalysis
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高影响因子
JOURNAL OF CATALYSIS
·
2019
·
IF 7.723
Rui Chen,Changjun Yang,Quanquan Zhang,Bingguang Zhang,Kejian Deng
A new iron tetra(2,3-bis(butylthio)maleonitrile)porphyrazine (FePz(SBu) 8 ) has been synthesized, then it was loaded on H-ZSM-5 zeolite to obtain a supported biomimetic photocatalyst H-ZSM-5/FePz(SBu) 8 . Using H 2 O 2 as oxidant, the photocatalytic selective oxidation of glucose in water under visible light (λ ≥ 420 nm) irradiation was carried out in presence of H-ZSM-5/FePz(SBu) 8 . Under such conditions, the glucose can be efficiently converted into value-added chemicals such as glucaric acid, gluconic acid, arabinose, glycerol and formic acid . More importantly, in comparison with pure FePz(SBu) 8 and pure H-ZSM-5 zeolite, the H-ZSM-5/FePz(SBu) 8 exhibited a higher photocatalytic activity for glucose oxidation and the formation of glucaric acid was observed only when H-ZSM-5/FePz(SBu) 8 was used, deriving from the synergistic effect between FePz(SBu) 8 and H-ZSM-5 zeolite. Some reaction parameters of glucose oxidation catalyzed by the H-ZSM-5/FePz(SBu) 8 were discussed, such as loading amount of FePz(SBu) 8 , H 2 O 2 :glucose ratio, glucose concentration, and so on. It was demonstrated that the Soret-band of FePz(SBu) 8 contributed more to the visible light photocatalytic activity than the Q-band during the photocatalytic process. The stability of H-ZSM-5/FePz(SBu) 8 during the photocatalytic process was further evaluated by the reusability test. In addition, the generation of reactive oxygen species was determined by electron spin resonance (ESR) technology and scavenger experiments. A possible reaction pathway of glucose oxidation was also discussed.
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高影响因子
PHYTOMEDICINE
·
2024
·
IF 6.7
Zhenxiu Liu,Lin Chen,Mingyun Chen,Lang Linghu,Zhihua Liao,Min Chen,Guowei Wang
Background Farnesoid X receptor (FXR) is a vital receptor for bile acids and plays an important role in the treatment of cholestatic liver disease. In addition to traditional bile acid-based steroidal agonists, synthetic alkaloids are the most commonly reported non-steroidal FXR agonists. Sarmentol H is a nor-sesquiterpenoid obtained from Sedum sarmentosum Bunge, and in vitro screening experiments have shown that it might be related to the regulation of the FXR pathway in a previous study. Purpose To investigate the therapeutic effects of sarmentol H on cholestasis and to determine whether sarmentol H directly targets FXR to mitigate cholestasis. Furthermore, this study aimed to explore the key amino acid residues involved in the binding of sarmentol H to FXR through site-directed mutagenesis. Methods An intrahepatic cholestasis mouse model was established to investigate the therapeutic effects of sarmentol H on cholestasis. In vitro experiments, including Co-Ip and FXR-EcRE-Luc assays, were performed to assess whether sarmentol H activates FXR by recruiting the receptor coactivator SRC1. CETSA, SIP, DARTS, and ITC were used to determine the binding of sarmentol H to FXR protein. The key amino acid residues for sarmentol H binding to FXR were analyzed by molecular docking and site-directed mutagenesis. Finally, we conducted in vivo experiments on wild-type and Fxr −/− mice to further validate the anticholestatic target of sarmentol H. Results Sarmentol H had significant ameliorative effects on the pathological conditions of cholestatic mice induced with ANIT. In vitro experiments suggested that it is capable of activating FXR and regulating downstream signaling pathways by recruiting SRC1. The target validation experiments showed that sarmentol H had the ability to bind to FXR as a ligand (K D = 2.55 μmol/L) and enhance the stability of its spatial structure. Moreover, site-directed mutagenesis revealed that THR292 and TYR365 were key binding sites for sarmentol H and FXR. Furthermore, knockout of the Fxr gene resulted in a significantly higher degree of ANIT-induced cholestatic liver injury than that in wild-type cholestatic mice, and the amelioration of cholestasis or regulatory effects on FXR downstream genes by sarmentol H also disappeared in Fxr −/− cholestatic mice. Conclusion Sarmentol H is an FXR agonist. This is the first study to show that it exerts a significant therapeutic effect on cholestatic mice, and can directly bind to FXR and activate it by recruiting the coactivator SRC1.
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DOI
PubMed
高影响因子
ADVANCED POWDER TECHNOLOGY
·
2024
·
IF 4.2
Hu Wen,Yuxin Li,Haitao Yin,Wei Wang,Zhengchao Jin,Shunyu Han,Nanzhe Jiang
The conversion of natural clay to crystalline zeolites has been the subject of considerable interest from both academic and industrial circles. We present an effective strategy for converting kaolin to ZSM-5 zeolite, addressing the issue of reduced mesopore formation in conventional nano-ZSM-5 aggregates due to close-packing. This strategy utilizes kaolin as the sole source of silicon and aluminum, and by decoupling the nucleation and growth of ZSM-5 crystals, loosely stacked nano-H-ZSM-5 aggregates with high crystallinity crystals can be synthesized in a solid-like system by employing a tiny amount of TPAOH (TPAOH/SiO 2 = 0.064). The resulting nano-H-ZSM-5 aggregates exhibited high specific surface area (405.66 m 2 /g), high mesopore volume (0.64 cm 3 /g), and superior catalytic activity. This strategy offers a novel approach to the cost-effective synthesis of nano-H-ZSM-5 aggregates suitable for industrial applications.
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高影响因子
Science Advances
·
2025
·Vol. 11
·期 29
·
IF 12.5
Zhenyu Li,Kunhong Jiang,Yue Yang,Yijing Pian,Huizhen Liu,Zexuan Zheng,Xiyang Wang,Subhajit Jana,Jiefei Li,Zhuoyuan Ma,Xiaoyun Qiao,Xiaoxin Zou,Xuelu Ma,Bin Zhang,Haibin Chu,Yimin A. Wu
Glycerol oxidation reaction (GOR) represents an economical pathway for transforming renewable feedstock to value-added chemicals. However, the inertness of C(sp 3 )─H bonds of glycerol and intermediates results in the high energy barrier of the dehydrogenation step, relating to poor product selectivity at high glycerol conversion. Here, a carbon nanotube–supported PdBO x @Pd heterostructure catalyst (PdBO x @Pd/CNTs) was synthesized in which in situ–exsoluted PdBO x clusters covalently covered Pd nanoparticles, thus yielding strong electronic interaction between Pd nanoparticles and PdBO x clusters. The strong electronic interaction in PdBO x @Pd/CNTs induces the hybridization between Pd(d), B(s, p), and O(s, p) atom orbits, optimizing the adsorption of reactants and intermediates, thus enhancing the activity for the GOR. The density functional theory calculation result reveals that the strong electronic interaction in PdBO x @Pd/CNTs facilitates the hydrogen transfer in the primary C─H bond of the CH 2 OHCHOHCH 2 O* intermediate, thus reducing the energy barrier of the rate-determining step and improving glyceric acid selectivity toward the GOR.
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DOI
PubMed
高影响因子
Carbon Energy
·
2025
·
IF 24.2
Chunfa Liu,Haoyun Bai,Jinxian Feng,Keyu An,Lun Li,Zhichao Yu,Lulu Qiao,Di Liu,Shuyang Peng,Hongchao Liu,Hui Pan
Large-scale green hydrogen production technology, based on the electrolysis of water powered by renewable energy, relies heavily on non-precious metal oxygen evolution reactions (OER) electrocatalysts with high activity and stability under industrial conditions (6 M KOH, 60°C–80°C) at large current density. Here, we construct Fe and Co co-incorporated nickel (oxy)hydroxide (Fe 2.5 Co 2.5 Ni 10 O y H z @NFF) via a multi-metal electrodeposition, which exhibits outstanding OER performance (overpotential: 185 mV @ 10 mA cm −2 ). Importantly, an overwhelming stability for more than 1100 h at 500 mA cm −2 under industrial conditions is achieved. Our combined experimental and computational investigation reveals the surface-reconstructed γ-NiOOH with a high valence state is the active layer, where the optimal (Fe, Co) co-incorporation tunes its electronic structure, changes the potential determining step, and reduces the energy barrier, leading to ultrahigh activity and stability. Our findings demonstrate a facile way to achieve an electrocatalyst with high performance for the industrial production of green hydrogen.
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高影响因子
RARE METALS
·
2023
·Vol. 43
·期 3
·1153-1166
·
IF 8.8
Lu Li-Wen,Luo Hui,Li Guang-Xu,Li Yun,Wang Xin-Hua,Huang Cun-Ke,Lan Zhi-Qiang,Zhou Wen-Zheng,Guo Jin,Ismail Mohammad,Liu Hai-Zhen
The Li-Mg-B-H composite (2LiBH 4 + MgH 2 ) has a high capacity of 11.4 wt% as a hydrogen storage material. However, the slow kinetics and poor cycling stability severely restrict its practical applications. In this work, a layered Nb 2 C MXene was first synthesized and then introduced to tailor the kinetics and cycling stability of the Li-Mg-B-H composite. The milled 2LiH + MgB 2 composites were initially hydrogenated to obtain the 2LiBH 4 + MgH 2 composites. The 2LiBH 4 + MgH 2 + 5 wt% Nb 2 C can release 9.0 wt% H 2 in 30 min at 400 °C, while it is only 2.7 wt% for the undoped 2LiBH 4 + MgH 2 . The dehydrogenation activation energies of MgH 2 and LiBH 4 are 123 and 154 kJ·mol −1 respectively for the 5 wt% Nb 2 C-doped composite, lower than the undoped composite (164 and 165 kJ·mol −1 ). The 2LiBH 4 + MgH 2 + 5 wt% Nb 2 C possesses excellent cycling stability, with the reversible capacity only slightly reduced from 9.4 wt% for the 1st cycle to 9.3 wt% for the 20th cycle. Nb 2 C keeps stable in the composite and acts as an efficient catalyst for the Li-Mg-B-H composite. It is believed that both the layered structure and the active Nb element contribute to the enhanced hydrogen storage performances of the Li-Mg-B-H composite. This work confirms that the Nb 2 C MXene with layered structure has a significant enhancing impact on the Li-Mg-B-H hydrogen storage materials, which is different from the bulk NbC. Graphical abstract
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高影响因子
Current Protocols
·
2022
·Vol. 2
·期 6
·e432
·
IF 0
An-Di Liu,Zhao-Li Wang,Li Liu,Liang Cheng
The photoredox synthesis of C-5 (hetero)arylated uracil and uridine substrates with the corresponding diazonium salts is described. The coupling proceeds efficiently without protection of the hydroxyls at the ribose or pre-functionalization of the C5 position at the nucleobase. No transition-metal catalyst is used in this transformation, thereby avoiding metal contamination in the final products. The use of water as the medium also eliminates the impurities caused by the use of organic solvents. © 2022 Wiley Periodicals LLC. Basic Protocol 1 : Synthesis of 5-aryl and 5-heteroaryl uracil derivatives Basic Protocol 2 : Synthesis of 5-aryl uridine and deoxyuridine uridine derivatives
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
·
IF 6.371
Wei Shen,Liang Qiao,Juan Ding,Yongming Sui
Tailoring tantalum disulfide (TaS 2 ) electrocatalysts with tunable stacking architecture and phase structure is of great importance for advancement of hydrogen evolution reaction (HER). In this work, stacking architecture- and phase- modulated tantalum disulfide nanosheets are reported through a facile liquid phase synthesis strategy. Accordion-like nanosheets , vertical nanosheets and ultrathin nanosheets are named according to their obvious stacking architecture, and 1 T-2 H mixed phase structures containing different degrees of 2 H phases are realized. High-resolution transmission electron microscopy shows that there are obvious lattice defects in the nanosheets. Tantalum disulfide nanosheets synergistically integrate multiple advantages of nanostructure engineering, phase engineering and defect engineering. In the HER process, the ultrathin tantalum disulfide nanosheet structure is conducive to the in-plane electron transfer , and its close contact with the electrode surface makes the charge transfer faster and has the best HER activity. The overpotential of the ultrathin nanosheet electrocatalyst at 10 mA cm −2 is 280 mV. After 10,000 CV cycles and over 40 h of i-t test, the catalyst still has high stability in acidic media. Theoretical calculations show that the addition of 2 H phase structure and rich defects improves the intrinsic activity and active sites, and jointly promotes the improvement of HER performance. Our work integrates a variety of optimal regulation methods into TaS 2 nanosheets, providing a new idea for the construction of advanced electrocatalysts for water electrolysis.
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高影响因子
ACS Catalysis
·
2026
·
IF 13.6
Wentao Hao,Zhuqian Wang,Hui Cao,Jia Qiao,Qingde Zhang,Kun Xiong,Xingchen Liu,Yong Qin,Chaoqiu Chen
The selective oxidation of CH4 to C2 oxygenates under mild conditions is a significant pathway for CH4 valorization, yet it remains extremely challenging due to the inertness of methane, the competing overoxidation, and sluggish C–C coupling kinetics. Here, we show that the N,S co-doped carbon nanotube-supported Fe5 clusters catalyst (Fe5/NSC) with adjacent Fe sites drives sequential C–H activation and C–C coupling to ethanol with a C2H5OH productivity of 1939.6 μmol·gcat–1·h–1 and a selectivity of 83.9% at 25 °C and 0.5 MPa CH4 without the assistance of CO. Comprehensive experimental investigation and density functional theory calculations reveal the critical role of adjacent Fe sites in the selective formation of C2H5OH. The adjacent Fe sites featured in Fe5/NSC synergistically facilitate the dissociation and/or partial oxidation of CH4 to distinct C1 intermediates (*OCH2 and *CH3) and subsequent OCHx–CHx coupling between them to form the key CH3CH2O* intermediate for C2H5OH production, as opposed to the conventional CHx–CO coupling pathway that primarily yields acetic acid.
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高影响因子
危险品化学品经营许可证（带存储）