JOURNAL OF THE EUROPEAN CERAMIC SOCIETY
·
2023
·
IF 5.7
Yuzhu Shen,Wei Sun,Yonglong Xu,Qingbo Wen,Hongbo Zhang,Xiang Xiong
In this study, to overcome the difficulties associated with the preparation of PyC-ceramic interface and controllable deposition of the structure, we initially used a two-step molten salt infiltration method to prepare a C/C-Me-Zr-Hf (Me = Ta, Si) composite with excellent oxyacetylene ablation performance. The microstructure and the behavior of ablative were addressed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) as well as by X-ray diffraction（XRD）. The results reveals that C/C-ZrHfC-SiC composite prepared by two-step molten salt infiltration method have a controllable ultra-high temperature ceramic structure and better ablation resistance.
研究领域:
材料科学
·
航空航天工程
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DOI
高影响因子
CERAMICS INTERNATIONAL
·
2023
·
IF 5.2
Hailong Pan,Shijie Yan,Yiyun Zhang,Jialun Du,Xiaoyu Zhang,Pijun Gong,Haitao Wu,Huanrong Tian,Michael Wübbenhorst
A series of Ce 2 [Zr 1- x (A) x ] 3 (MoO 4 ) 9 (A = Sr 1/3 Ta 2/3 , Sr 1/3 Sb 2/3 ; x = 0.02, 0.04, 0.06, 0.08 and 0.10) (abbreviated as CZ 1- x T x and CZ 1- x S x ) microwave dielectric ceramics were studied systematically with respect to microstructures, sintering behaviors, crystal structures, microwave dielectric properties and infrared vibrational modes. Density measurements and scanning electron microscopy (SEM) reveal the dense and homogeneous microstructures. X-ray diffraction (XRD) results confirm the formation of solid solutions belonging to the hexagonal system with a R 3 ‾ c space group, and the lattice volume increases with raising the doping content. Furthermore, the complex chemical bond theory was used to calculate the intrinsic bond parameters, and the correlations between the microwave dielectric properties and intrinsic bond parameters were established. Finally, far infrared (FIR) spectra reveal that the main polarization contribution stems from the absorptions of the phonon oscillations in these two groups of ceramics. Typically, the optimum microwave dielectric properties are achieved for CZ 0.9 T 0.1 and CZ 0.94 S 0.06 ceramics with ε r = 10.24, Q × f = 92,009 GHz (at 9.70 GHz), τ f = −8.84 ppm °C −1 and ε r = 10.40, Q × f = 82,696 GHz (at 9.69 GHz) and τ f = −8.04 ppm °C −1 , respectively. Interestingly, the CZ 0.9 T 0.1 ceramic exhibits the maximum Q × f value in the ion doped Ce 2 Zr 3 (MoO 4 ) 9 ceramics while retaining a good τ f = −8.84 ppm °C −1 .
研究领域:
材料科学
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陶瓷
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介电材料
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固体化学
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微波工程
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DOI
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2022
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IF 10.319
Liang Xu,Lei Su,Hongjie Wang,Hongfei Gao,Pengfei Guo,Min Niu,Kang Peng,Lei Zhuang,Zhiwei Dai
Materials with ultralow thermal conductivity and good thermal stability are of great interest in numerous applications such as energy storage and conversion devices, and thermal insulation components. In this work, a family of high-entropy Sm 2 B 2 O 7 (B=Ti, Zr, Sn, Hf, Y, Yb, Nb, and Ta) oxides with highly disordered cations on the B-site has been synthesized by introducing large atomic-size mismatch, mass and charge disorder. Through tuning the composition, the high-entropy Sm 2 B 2 O 7 oxides can be engineered from pyrochlore to fluorite structure, accompanied with an order-disorder transition. The pyrochlore Sm 2 (Nb 0.2 Sn 0.2 Ti 0.2 Y 0.2 Zr 0.2 ) 2 O 7 and fluorite Sm 2 (Nb 0.2 Ta 0.2 Y 0.2 Yb 0.2 Zr 0.2 ) 2 O 7 exhibit low thermal conductivities of 1.35 W·m −1 ·K −1 and 1.23 W·m −1 ·K −1 , respectively, indicating their good thermal insulation. In addition, the high-entropy fluorite Sm 2 (Nb 0.2 Ta 0.2 Y 0.2 Yb 0.2 Zr 0.2 ) 2 O 7 also shows average thermal expansion coefficient of 10.2 × 10 −6 °C −1 and high-temperature stability even after thermal exposure at 1600 °C in air for 30 h. These results indicate that the high-entropy Sm 2 B 2 O 7 (B=Ti, Zr, Sn, Hf, Y, Yb, Nb, and Ta) can be promising candidates for thermal barrier coatings and thermally insulators.
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高影响因子
REACTIVE & FUNCTIONAL POLYMERS
·
2023
·
IF 5.1
Yuxuan Ma,Yajing Sun,Jifeng Guo,Xiao Wei
In this work, a novel in-situ synthetic TA-APTES NPs multifunctional imprinted membrane was fabricated by tanning-inspired coating for selective adsorption of tetrabromobisphenol a (TBBPA) and oil-water emulsion separation. Tannic acid (TA) from natural plants can be cross-linked with 3-aminopropyltriethoxysilane (APTES) by a simple green method to form nanosphere structures with secondary reaction sites. With TA-APTES coating, the membrane can be quickly converted from hydrophobic to super-hydrophilic. TEOS is not only used as a cross-linking agent in imprinting process，but also can be used for TA-APTES hybridization on the membrane surface to introduce stable silicone hydroxyl groups to the membrane surface. The modified membranes showed good hydrophilicity with a water flux of 27,272Lm −2 h −1 at 0.1Mpa, which was 18 times higher than that of pure PVDF membranes. In addition, the separation efficiency of four different types of oil-water emulsions (n-hexane, petroleum ether, dichloromethane and kerosene) reached 99.6%, 98.3%, 95.6%, and 98.7%, respectively. Among them, the oil water emulsion flux of dichloromethane could reach 1000.1. what's more, the prepared membranes also maintained relatively high selective separation efficiencies of TBBPA in oil-water mixtures. To better explain the mechanism of the TBBPA reaction process, the active sites in the TBBPA reaction process were calculated and predicted by density generalization theory (DFT). The Br and phenolic hydroxyl groups on the benzene ring of TBBPA showed higher activity and might be the main reaction sites. In addition, the imprinted composite membranes can be easily regenerated and reused without performance loss through a simple cleaning process. The coating process inspired by natural polyphenol chemistry has the advantage of being green, cost-effective and low energy, showing real potential in multifunctional membrane applications.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
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2024
·
IF 7.7
Ziqing Hu,Xianling Wei,Xiaoyan Liu,Weidong Bai,Xiaofang Zeng
This study compounded natural corn starch (CS), mung bean starch (MBS) and potato starch (PS) with tannic acid (TA) to stabilize O/W Pickering emulsion. The effect of TA/starch mass ratio (0–0.25) and three starch categories on particle properties, emulsifying properties, lipid oxidation, freeze-thaw stability, emulsion powder and digestive properties were comprehensibly investigated. In detail, the TA/starch complexes size increased gradually (91.14 nm–200.87 nm) and the hydrophobicity first increased and then decreased (TA/CS > TA/MBS > TA/PS) with increasing TA/starch mass ratio. In addition, the emulsifying ability of TA/starch complexes also increased first and then decreased with increasing mass ratio, especially TA/CS system was the best, which was the same as the hydrophobicity conclusion ( θ ow = 80.46°). Moreover, four starch-based emulsion application characteristics were further evaluated to reveal interface structure. Compared to CS and PS system, TA/MBS emulsion had stronger ability to resist the oil oxidation (TBA = 2.54 μg/mL), destruction of ice crystal (whiter emulsion powder) and digestive enzymes (FFAs = 75.33 %). It mainly attributed to the crosslinking network structure and the highest surface load of TA/MBS complexes. This study would provide new ideas for the design and application of emulsifying properties and emulsion stability.
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DOI
PubMed
高影响因子
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
·
2024
·
IF 3.5
Hongbin An,Ruoyu Chen,Saisai Li,Lingfeng Huang,Wenbao Jia,Qianfang Wu,Aiqing Mao
Powder synthesis is crucial for achieving the densification and facilitating widespread applications of high entropy carbide (HEC). Specifically, the production of fine particle-size powders is essential to enhance the densification of HECs. Consequently, this paper proposes the molten salt method for synthesizing HEC powders. The synthesis process successfully yielded (Ta Nb Ti V) C powders with a particle size of only 0.44 µm at 1400°C, exhibiting a uniform distribution of each element. Subsequent densification of (Ta Nb Ti V) C within the 1700–1900°C temperature range was carried out using spark plasma sintering. It was observed that as the densification temperature increased, the densification and mechanical properties of HEC significantly improved. This study presents innovative ideas for the preparation of HEC at lower temperatures.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2024
·
IF 7.7
Jingxuan Zhao,Hongxu Liu,Yuanhang Zhao,Yuchao Qi,Ruijia Wang,Ziwei Lv,Yang Yu,Shulin Sun,Yiming Wang,Aihua Xie
Currently, the most effective way to improve the anti-fouling performance of water treatment separation membrane is to enhance the hydrophilicity of the membrane surface, but it can still cause contamination, leading to the occurrence of flux reduction. The construction of a strong hydration layer to resist wastewater contamination is still a challenging task. In this study, a defect-free hydration layer barrier was achieved by grafting chitosan polysaccharide derivatives (CS-SDAEM) on the membrane, which achieved in effective fouling prevention and low flux decline rate. A layer of tannic acid-coated carbon nanotubes (TA@CNTs) has been uniformly deposited on the commercial PVDF membrane so that the surface was rich in -COOH groups, providing sufficient reaction sites. These reactive groups facilitate the grafting of amphiphilic polymers onto the membrane. This modification strategy achieved in enhancing the antifouling performance. The modified membrane achieved low contamination rate with DR of 16.9 % for wastewater filtration, and the flux recovery rate was above 95 % with PWF of 1100 (L·m −2 ·h −1 ). The membrane had excellent anti-fouling performance, which provided a new route for the future development of water treatment membrane.
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PubMed
高影响因子
FUEL
·
2024
·
IF 6.7
Sanjiang Pan,Zishuo Xie,Hang Li,Shenao Wang,Yang Fu,Desong Wang
Considering the regional distribution of freshwater resources, acquiring hydrogen by seawater electrolysis has lower cost and feasibility. NiCoFe-based materials have been widely studied due to their excellent catalytic oxidation performance in freshwater. However, the large amount of chloride ions in seawater will severely erode the catalytic site and greatly reduce the catalyst's lifetime. In this paper, a two-dimensional nanosheet quaternary metal hydroxide electrode composed of Ni, Co, Fe, and Ta elements was synthesized via a facile one-step hydrothermal method for efficient oxygen evolution reaction (OER) in seawater electrolysis. Structural characterization and in-situ test revealed that the incorporation of Ta not only optimized the electronic structure of the catalyst but also accelerated the formation of the γ-NiOOH phase, making the active phase is protected from being attacked by Cl - ions during the formation process, enhancing its OER activity while achieving extended durability. The catalyst was operated at an ampere-level of 1 A cm -2 for over one month (800 h), and no significant degradation was observed. This work provides a promising strategy for developing cost-effective, efficient, and stable catalysts for challenging applications in seawater electrolysis.
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高影响因子
Journal of Molecular Cell Biology
·
2024
·
IF 5.3
Ye Jing,Huang Xiyu,Yuan Manman,Wang Jinglin,Jia Ru,Wang Tianyi,Tan Yang,Zhu Shun,Xu Qiang,Wu Xingxin
The rs72613567:TA polymorphism in 17-beta hydroxysteroid dehydrogenase 13 (HSD17B13) has been found to reduce the progression from steatosis to nonalcoholic steatohepatitis. In this study, we sought to define the pathogenic role of HSD17B13 in triggering liver inflammation. Here we find that HSD17B13 forms liquid–liquid phase separation (LLPS) around lipid droplets in the livers of nonalcoholic steatohepatitis patients. The dimerization of HSD17B13 supports the LLPS formation and promotes its enzymatic function. HSD17B13 LLPS increases the biosynthesis of platelet activating factor (PAF), which in turn promotes fibrinogen synthesis and leukocyte adhesion. Blockade of PAFR or STAT3 pathway inhibited the fibrinogen synthesis and leukocyte adhesion. Importantly, adeno-associated viral-mediated xeno-expression of human HSD17B13 exacerbated western diet/carbon tetrachloride-induced liver inflammation in Hsd17b13−/− mice. In conclusion, our results suggest that HSD17B13 LLPS triggers liver inflammation by promoting PAF-mediated leukocyte adhesion, and targeting HSD17B13 phase transition could be a promising therapeutic approach for treating hepatic inflammation in chronic liver disease.
研究领域:
分子生物学
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细胞生物学
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肝病学
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炎症
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遗传学
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PubMed
高影响因子
Nano Research
·
2020
·Vol. 14
·期 1
·222-231
·
IF 8.183
Zhu Huimin,Cao Guodong,Fu Yike,Fang Chao,Chu Qiang,Li Xiang,Wu Yulian,Han Gaorong
Multidrug resistance (MDR) restricts chemotherapy efficacy due to P-glycoprotein (P-gp) mediated drug efflux, whereas current approaches to suppressing P-gp expression suffer from intrinsic challenges, such as low transfection, high toxicity and poor specificity. Here, hollow ferric-tannic acid complex nanocapsules (HFe-TA), which can be effectively degraded by the reaction with adenosine triphosphate (ATP), are synthesized for the delivery of glucose oxidase (GOx) and doxorubicin (DOX) for tumor treatment. The findings indicate that the intracellular ATP is significantly decreased due to the combined effect of HFe-TA degradation and GOx-mediated glucose consumption. Along with this ATP down-regulation, P-gp expression of tumor cells is suppressed remarkably, which in turn promotes the intracellular accumulation and anticancer efficacy of DOX. In addition, the production of OH by Fe ions released from HFe-TA is promoted by the by-products of the oxidation of glucose process by GOx. In consequence, HFe-TA nanocapsules loaded with DOX and GOx enable significant inhibition effect to tumors both in vitro and in vivo due to the synergistic effect of cascade reactions. This study has therefore provided an alternative therapeutic platform for effective tumor inhibition with the potential in overcoming intrinsic MDR.
研究领域:
纳米技术
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药学
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癌症研究
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生物医学工程
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DOI
高影响因子
Materials Today Chemistry
·
2025
·
IF 6.7
Ting Zhang,Ruyi Zhao,Bin Yang,Jiaojiao Sang,Zhengzhi Zheng,Tianyu Lu,Xinyu Li,Zihao Xu,Rui Hu,Zihao Lv,Ru Xia,Jiasheng Qian,Ning Jia
Addressing the demand for high-thermal-conductivity composites in flexible electronics thermal management, this study designed a bioinspired composite film based on bacterial cellulose (BC) nanofibers as the flexible matrix. The MXene@TA-Ag/BC (MTAB) composite film with a “brick-and-mortar” biomimetic structure was constructed through vacuum-assisted filtration and hot-pressing processes, incorporating tannic acid (TA)-modified MXene nanosheets with in situ loaded silver nanoparticles (AgNPs). The dihydroxy groups of TA not only facilitated the uniform deposition of AgNPs on MXene surfaces but also formed multiple hydrogen bonds with the BC matrix, significantly enhancing interfacial compatibility. When the mass fraction of the composite filler reached 40 %, the in-plane thermal conductivity of the as-prepared composite films significantly increased from 2.66 W/m·K (of pure BC films) to 10.99 W/m·K, representing an increase of 313.8 % in comparison to that of pure BC matrix. Mechanical characterization further revealed remarkable tensile strength (114.8 MPa), primarily attributed to synergistic stress-transfer between MXene@TA-Ag fillers and the BC matrix. Thermogravimetric analysis demonstrated superior thermal stability with a maximum decomposition temperature of 277.4 °C, indicating suitability for high-temperature applications.The present work achieved synergistic optimization of thermal and mechanical properties through a multi-scale interfacial engineering strategy, offering new insights for developing next-generation flexible thermal interface materials.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2021
·
IF 5.316
Yongwei Zhang,Sining Yun,Xinying Qiao,Menglong Sun,Jiaoe Dang,Changwei Dang,Jingjing Yang
Developing high-performance and low-cost catalysts for replacing Pt-based catalysts is a significant challenge for solar cells and water splitting applications. In this work, a bifunctional hybrid catalyst of MnTa 2 O 6 @MPC (MPC: mesh-like bio-based porous carbon) was synthesized, using a co-precipitation approach. Benefiting from the high specific surface area (332.743 m 2 g −1 ), integrating the merits of the electrical conductivity of MPC, the outstanding electrocatalytic ability of MnTa 2 O 6 , and the synergistic effect between MnTa 2 O 6 and MPC, the catalytic activity of MnTa 2 O 6 @MPC was significantly enhanced. To boost the photovoltaic performance of dye-sensitized solar cells, a novel Cu 2+ /Cu + redox mediator and dye (Y123, D35) were adopted for replacing the traditional I 3 - /I - redox mediator and N719 dye, respectively. The resulting advanced solar cell with the Cu 2+ /Cu + redox mediator based on the MnTa 2 O 6 @MPC counter electrode catalyst exhibited a photovoltage of ~0.88 V, and cell efficiencies of 3.41% and 1.92% for the D35 and Y123 dye systems, respectively, which are respectively 16% and 8% higher than that of Pt. MnTa 2 O 6 @MPC also exhibited significant catalytic ability for hydrogen production, yielding a small overpotential of 141.9 mV at a current density of 10 mA cm −2 and a small Tafel slope of 105.0 mV dec −1 in an alkaline medium. This work provides promising guidance for designing bifunctional hybrid electrocatalysts for high-performance new energy devices.
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