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61.
Wenhui Zhu Haizhen Huan Ying Bu Xuepeng Li David Shiuan Jianrong Li Xiaotao Sun 《International Journal of Food Science & Technology》2019,54(6):2159-2168
Protein oxidation is considered as an important issue in food preservation process. In the present study, the potential influence of protein oxidation on water holding capacity and protein structure of jumbo squid (Dosidicus gigas) mantle was investigated. After the hydroxyl radical oxidation, it was found that the carbonyl, surface hydrophobicity and dityrosine content of myofibrillar protein significantly increased (P < 0.05), while the content of total sulphydryl decreased significantly (P < 0.01). Meanwhile, the fluorescence intensity of squid was weakened, and the maximum absorption peak of fluorescence red shift as the H2O2 concentration increased. The sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) showed that not only the protein cross-linking but also degradation could have occurred. The content of α-helix decreased, the content of β-sheet, β-turn and the unordered structures increased after oxidation. In addition, oxidation resulted in a decrease in water holding capacity. Taken together, oxidation resulted in the damage of the myofibrillar structure, the increase in muscle loss rate and the decrease in water holding capacity. 相似文献
62.
Liangkai Liu Qihua Zhu Qiangqiang Zhu Benxue Jiang Minghui Feng Long Zhang 《Ceramics International》2019,45(5):5339-5345
Y2O3 ceramic is a promising optical material for mid-infrared (IR) windows and domes. Improvements in the mechanical and thermal performance of this material have become urgent if it is to perform adequately under extreme conditions. Herein, Y2O3 nanopowders were produced through the nitrate pyrogenation method. The final Y2O3 transparent ceramics were fabricated with a hybrid sintering method combining low temperature presintering and a subsequent hot isostatic pressing (HIP) treatment. The synthesis of nanopowders and the fabrication of the final ceramic products were investigated in detail. The Y2O3 ceramic sample that was presintered at 1350?°C provided the optimum microstructure for HIP treatment and resulted in an average grain size of 0.5?µm. Owing to the reduced grain size, the flexure strength and Vickers hardness of the sample were improved to 180?MPa and 8.4?GPa, respectively. Furthermore, the achieved pure Y2O3 ceramic demonstrated an excellent thermal conductivity at high temperature. 相似文献
63.
Pin Liu Yujing Zhang Yiwei Zhu Baoyan Fan Wenru Li Haibo Zhang Shenglin Jiang 《Journal of the American Ceramic Society》2019,102(4):1912-1920
Energy storage capacitors with high recoverable energy density and efficiency are greatly desired in pulse power system. In this study, the energy density and efficiency were enhanced in Mn-modified (Pb0.93Ba0.04La0.02)(Zr0.65Sn0.3Ti0.05)O3 antiferroelectric ceramics via a conventional solid-state reaction process. The improvement was attributed to the change in the antiferroelectric-to-ferroelectric phase transition electric field (EF) and the ferroelectric-to-antiferroelectric phase transition electric field (EA) with a small Mn addition. Mn ions as acceptors, which gave rise to the structure variation, significantly influenced the microstructures, dielectric properties and energy storage performance of the antiferroelectric ceramics. A maximum recoverable energy density of 2.64 J/cm3 with an efficiency of 73% was achieved when x = 0.005, which was 40% higher than that (1.84 J/cm3, 68%) of the pure ceramic counterparts. The results demonstrate that the acceptor modification is an effective way to improve the energy storage density and efficiency of antiferroelectric ceramics by inducing a structure variation and the (Pb0.93Ba0.04La0.02)(Zr0.65Sn0.3Ti0.05)O3-xMn2O3 antiferroelectric ceramics are a promising energy storage material with high-power density. 相似文献
64.
Meng Zhu Xiaojuan Zhang Yanxia Su Yiguang Wang Yibo Wu Dan Yang Hao Wang Min Zhang Min Zhang Quan Chen Nanwen Li 《应用聚合物科学杂志》2019,136(15):47370
To improve the properties of diblock copolystyrene-based anion exchange membranes (AEMs), a series of AEMs with comb-shaped quaternary ammonium (QA) architecture (QA-PSm-b-PDVPPAn-xC where x denotes the number of carbon atoms in different alkyl tail chains and has values of 1, 4, 8, and 10 and C denotes carbon) were designed and synthesized via subsequent quaternization reactions with three different alkyl halogens (methyl iodide and N-alkane bromines (CH3[CH2] x-1Br where x = 4, 8, and 10). Compared with triblock analogues quaternized with methyl iodide in our previous research, QA-PSm-b-PDVPPAn-xC (x = 4, 8, and 10) AEMs are more flexible with the introduction of a long alkyl tail chain; this probably impedes crystallization of the rigid polystyrene-based main chain and induces sterically adjustable ionic association. An increase in the pendant alkyl tail chain length generally led to enhanced microphase separation of the obtained AEMs, and this was confirmed using small-angle X-ray scattering and atomic force microscopy. The highest conductivity (25.5 mS cm−1) was observed for QA-PS120-b-PDVPPA80-10C (IEC = 1.94 meq g–1) at 20 °C. Furthermore, the water uptake (<30%) and swelling ratio (<13.1%) of QA-PSm-b-PDVPPAn-xC AEMs are less than half of these corresponding values for their triblock counterparts. The QA-PS120-b-PDVPPA80-10C membrane retained a maximum stability that was as high as 86.8% of its initial conductivity after a 40-day test (10 M NaOH, 80 °C), and this was probably because of the steric shielding of the cationic domains that were surrounded by the longest alkyl tail chains. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47370. 相似文献
65.
Hehuan Cao Jidong Cao Fanghui Wang Shuxian Di Hong Zhu Min Pu Andzhela Bulanova 《International Journal of Hydrogen Energy》2021,46(35):18284-18293
To accelerate the commercialization of fuel cells, many efforts have been made to develope highly active and durable Pt-based catalyst for oxygen reduction reaction (ORR). Herein, PtCu porous nanowires (PNWs) with controllable composition are synthesized through an ultrasound-assisted galvanic replacement reaction. The porous structure, surface strain, and electronic property of PtCu PNWs are optimized by tuning composition, which can improve activity for ORR. Electrochemical tests reveal that the mass activity of Pt0.5Cu0.5 PNWs (Pt/Cu atomic ratio of 1:1) reaches 0.80 A mgPt?1, which is about 5 times higher than that of the commercial Pt/C catalyst. Notably, the improved activity of the porous nanowire catalyst is also confirmed in the single-cell test. In addition, the large contact area with the carrier and internal interconnection structure of Pt0.5Cu0.5 PNWs enables them to exhibit much better durability than the commercial Pt/C catalyst and Pt0.5Cu0.5 nanotubes in accelerated durability test. 相似文献
66.
Lin Chen Jun Guo Yuke Zhu Mingyu Hu Jing Feng 《Journal of the American Ceramic Society》2021,104(1):404-412
The features of crystal structures, thermo-mechanical properties and their dominant mechanisms of weberites RE3NbO7 were studied as high-temperature oxides. We concentrated on connections between structures and thermo-mechanical properties, the influences of bond lengths, lattice distortion degrees and microstructures on these properties were estimated. The shortening of bond length and increment of bonding strength would lead to the increase of mechanical properties. The Vickers hardness (4.5-7.8 GPa) and toughness (0.5-1.6 MPa·m1/2) of weberites RE3NbO7 are enhanced by grain refinement and increment of bond strength, while crystal structures, bond lengths, and lattice distortion degrees influenced their Young's modulus (100-170 GPa). Nano-indentation was applied to test the influence of microstructures on modulus and hardness. The dominant mechanisms for mechanical properties and thermal conductivity were proposed, which was conducive to properties tailoring and engineering applications of weberites RE3NbO7 oxides. 相似文献
67.
Andrew N. Kuhn Haidong Zhao Uzoma O. Nwabara Xiaofei Lu Mingyan Liu Yung-Tin Pan Wenjin Zhu Paul J. A. Kenis Hong Yang 《Advanced functional materials》2021,31(26):2101668
Copper catalysts are widely studied for the electroreduction of carbon dioxide (CO2) to value-added hydrocarbon products. Controlling the surface composition of copper nanomaterials may provide the electronic and structural properties necessary for carbon-carbon coupling, thus increasing the Faradaic efficiency (FE) towards ethylene and other multi-carbon (C2+) products. Synthesis and catalytic study of silver-coated copper nanoparticles (Cu@Ag NPs) for the reduction of CO2 are presented. Bimetallic CuAg NPs are typically difficult to produce due to the bulk immiscibility between these two metals. Slow injection of the silver precursor, concentrations of organic capping agents, and gas environment proved critical to control the size and metal distribution of the Cu@Ag NPs. The optimized Cu@Ag electrocatalyst exhibited a very low onset cell potential of −2.25 V for ethylene formation, reaching a FE towards C2+ products (FEC2+) of 43% at −2.50 V, which is 1.0 V lower than a reference Cu catalyst to reach a similar FEC2+. The high ethylene formation at low potentials is attributed to enhanced C C coupling on the Ag enriched shell of the Cu@Ag electrocatalysts. This study offers a new catalyst design towards increasing the efficiency for the electroreduction of CO2 to value-added chemicals. 相似文献
68.
Ziming Cai Peizhong Feng Chaoqiong Zhu Xiaohui Wang 《Journal of the European Ceramic Society》2021,41(4):2533-2538
Dielectric breakdown is a fundamental issue for ferroelectric ceramics. In this work, a phase-field method is introduced to study the breakdown behavior of ferroelectric ceramics with pores randomly distributed. Effects of the position and the size of pores on the breakdown behavior are analyzed. Results indicate that the position of pores, for example in grains or at grain boundaries, has a significant influence on the breakdown strength of ferroelectric ceramics. The nominal breakdown strength of ferroelectric ceramics with 2 % pores at grain boundaries is almost 50 % higher than 2 % pores in grains. Further, for ferroelectric ceramics with a certain porosity, the smaller the pore size, the higher the breakdown strength. As the nominal pore size decreases from 2.5 to 1, the nominal breakdown strength is enhanced from 0.73 to 1.16. Such results agree well with the widely accepted Gerson-Marshall model and previously published experimental observations. 相似文献
69.
Qiang Liu Xinyu Mao Xiaoying Li Penghui Chen Xin Liu Ziyu Liu Danyang Zhu Haohong Chen Tengfei Xie Jiang Li 《Journal of the American Ceramic Society》2021,104(10):4927-4931
0.5 at.% Cr:ZnGa2O4 precursor was synthesized by the co-precipitation method with nitrates as raw materials, using ammonium carbonate as the precipitant. Low-agglomerated Cr:ZnGa2O4 powders with an average particle size of 43 nm were obtained by calcining the precursor at 900℃ for 4 h. Using the powders as starting materials, 0.5 at.% Cr:ZnGa2O4 ceramics with an average grain size of about 515 nm were prepared by presintering at 1150℃ for 5 h in air and HIP post-treatment at 1100℃ for 3 h under 200 MPa Ar. The in-line transmittance of 0.5 at.% Cr:ZnGa2O4 ceramics with a thickness of 1.3 mm reaches 59.5% at the wavelength of 700 nm. The Cr:ZnGa2O4 ceramics can be effectively excited by visible light and produce persistent luminescence at 700 nm. For Cr:ZnGa2O4 transparent ceramics, the brightness of afterglow was larger than 0.32 mcd/m2 after 30 min, which is far superior to that of Cr:ZnGa2O4 persistent luminescence powders. 相似文献
70.