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41.
42.
Yuxi Guo Xuefeng Chen Pin Gong Fuxin Chen Dandan Cui Mengrao Wang 《International Journal of Food Science & Technology》2021,56(10):4970-4982
In vitro digestion models are widely used to study the structural changes, digestion and release of food components under simulated gastrointestinal conditions. As compared to the in vivo digestion tests, the in vitro digestion reflects the digestion and utilisation of food after ingestion and has the advantages of being time consuming, inexpensive, reproducible and free from moral and ethical restrictions. This study reviewed the current research studies on the in vitro simulated digestion of polysaccharides conducted in the last 5 years and focused on the oral, gastric and intestinal digestion models, with the aim of providing a basis for the further testing of changes in the content, structure and active ingredients of polysaccharides before and after digestion. 相似文献
43.
Jiajia Lu Guangfu Qian Lin Luo Huibing He Shibin Yin 《International Journal of Hydrogen Energy》2021,46(1):676-682
The tungsten trioxide attracts less attention due to the low electron transfer kinetics that hinders the interaction of electrons and ions during the hydrogen evolution reaction (HER). But the oxygen vacancy strategy can inspire its electrocatalytic activity for HER because it has a positive effect on improving the charge transfer and compensating for the weak hydrogen adsorption of the tungsten trioxide. By synthesizing a series of substoichiometric tungsten oxides, we reveal the linear relationship between the catalytic activity and the content of oxygen vacancies, which indicates that the oxygen vacancy strategy is an achievable route to enhance the HER for metal oxides. 相似文献
44.
Carboxyl-terminated polybutadiene (CTPB) is a widely used telechelic liquid rubber, which is mainly prepared by anionic or free-radical polymerization of 1,3-butadiene. It is known that the microstructure of liquid polybutadiene rubber largely affects its processability and mechanical properties. However, it is hard to control its microstructure in the free radical or anionic polymerization. In this study, a series of CTPB with high cis-1,4 content has been prepared for the first time via the oxidolysis and selective oxidation of cis-polybutadiene rubber (BR). Hydrogenation of their CC double bonds with p-toluenesulfonyl hydrazide/tri-n-propylamine (TSH/TPA) reagents afforded carboxyl-terminated polyethylenes (CTPE). For comparison, commercial CTPB (FCTPB), prepared by free-radical polymerization of 1,3-butadiene, was also hydrogenated and gave FCTPE with more ethyl branches. Linear CTPE (L-CTPE) was synthesized by ring-opening metathesis polymerization of 1,5-cyclooctadiene in the presence of maleic acid and subsequent hydrogenation. The microstructure of the polymers was established by FT-IR, 1H NMR, 13C NMR, and GPC and their thermal properties were determined by DSC and TGA. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 46934. 相似文献
45.
As an industrial solid waste, pyrite cinder exhibited excellent reactivity and cycle stability in chemical looping combustion. Prior to the experiment, oxygen carriers often experienced a high temperature calcination process to stabilize the physico-chemical properties, which presented significant influence on the redox performance of oxygen carriers. However, the effect of calcination temperature on the cyclic reaction performance of pyrite cinder has not been studied in detail. In this work, the effect of calcination temperature on the redox activity and attrition characteristic of pyrite cinder were studied in a fluidized-bed reactor using CH4 as fuel. A series of pyrite cinder samples were prepared by controlling the calcination temperature. The redox activity and attrition rate of the obtained pyrite cinder samples were investigated deeply. The results showed that calcination temperature displayed significant impact on the redox performance of pyrite cinder. Considering CH4 conversion (80%–85%) and attrition resistance, the pyrite cinder calcined at 1050?℃ presented excellent redox properties. In the whole experiment process, the CO2 selectivity of the pyrite cinder samples were not affected by the calcination temperature and were still close to 100%. The results can provide reference for optimizing the calcination temperature of pyrite cinder during chemical looping process. 相似文献
46.
Journal of Chemical Ecology - The cotton bollworm, Helicoverpa armigera, is one of the most destructive agricultural pests in the world, infesting cotton, maize, soybean, and many other crops. In... 相似文献
47.
Yunliang Yue Buwei Wang Nanxi Miao Chao Jiang Hongwei Lu Bowen Zhang Yankai Wu Jie Ren Min Wang 《Ceramics International》2021,47(2):2367-2373
The effects of strain on the magnetic properties of Zr2N MXene have been investigated by the first-principles calculations. The ground state of strain-free Zr2N MXene is intrinsically antiferromagnetic. However, the magnetic state of Zr2N MXene tends to be ferromagnetic when the applied strain is higher than 4%. The transition of magnetic orderings from antiferromagnetism to ferromagnetism under tensile strains can be understood from the Stoner criterion. Besides, the critical temperature (Tc) is about 470 K for the strain-free Zr2N MXene, indicating that the antiferromagnetic ordering can be robust and maintained at room temperature. The Tc of antiferromagnetic states begins to decrease once the strain is exerted. As the FM ordering is favored, however, the Tc then increases with the applied strain. Under 8% tensile strain, the Tc comes to room temperature (300 K). In addition, both the orientation of easy-axis and the magnetic anisotropy energy (MAE) of Zr2N MXene fluctuate with the strain. At the strain of 2%, the MAE reaches the largest (203 μeV per Zr atom), mainly resulting from the spin-orbit interactions between occupied and unoccupied px/py states of Zr atoms. All these tunable and appealing properties make Zr2N MXene desirable for spintronic applications. 相似文献
48.
This work aimed to study the comprehensive effects of photo-oxidation and biodegradation on different failure stages of polyester coatings,which were exposed to the tropical rainforest atmosphere.The surface morphology,aging products,local aging characteristics and electrochemical behavior of the coatings were characterized with scanning electron microscope(SEM),fourier transform infrared spectroscopy(FTIR),electrochemical impedance spectroscopy(EIS)and high-resolution dispersive Raman microscope.The results showed that the surface of coatings became rougher and fungal hyphae distributed more densely on surface with the increasing of exposure time.From the aspect of polymer structure,the ultraviolet radiation destroyed the main chain of polyester through the photo-oxidation process,resulting in the breakage of aliphatic ester bonds and the formation of esters.Further,the metabolites of fungi can promote the hydrolysis of oligomers produced by the photo-oxidation.In a short,the photo-oxidation could facilitate the biodegradation of the coating.With the synergistic effect of UV photo-oxidation and fungal biodegradation,a rapid diffusion tunnel between the coating surface and the metal substrate was established at the pore defects of the coating,which finally accelerated the corrosion failure process of the coating.The main corrosion products includeα-Fe2O3,ZnO and Zn5(OH)6(CO3)2. 相似文献
49.
50.
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