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消失模铸造EPS泡沫分解过程的三维数值模拟 被引量:6
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作者 张志莲 肖云峰 《铸造》 CAS CSCD 北大核心 2010年第10期1057-1060,共4页
消失模泡沫分解、析出过程直接影响金属的充型能力,文中采用数值模拟方法,研究了消失模铸造泡沫分解过程的流体动力学特性,预测了泡沫残留物的产生以及对最终铸件质量的影响,并通过实际发动机缸体进行验证,表明模拟值与实际测量值基本... 消失模泡沫分解、析出过程直接影响金属的充型能力,文中采用数值模拟方法,研究了消失模铸造泡沫分解过程的流体动力学特性,预测了泡沫残留物的产生以及对最终铸件质量的影响,并通过实际发动机缸体进行验证,表明模拟值与实际测量值基本吻合。 展开更多
关键词 消失模 数值计算 泡沫分解 充型能力
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PREPARATION OF POLYELECTROLYTE MULTILAYER COATED MICROBUBBLES FOR USE AS ULTRASOUND CONTRAST AGENT 被引量:1
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作者 Zhan-wen Xing Heng-te Ke +3 位作者 Shao-qin Liu Zhi-fei Dai Jin-rui Wang Ji-bin Liu 《Chinese Medical Sciences Journal》 CAS CSCD 2008年第2期103-107,共5页
Objeelive To prepare and characterize polyelectrolyte multilayer film coated microbubbles for use as ultrasound contrast agent (UCA) and evaluate its effects in ultrasonic imaging on normal rabbit's fiver parenchym... Objeelive To prepare and characterize polyelectrolyte multilayer film coated microbubbles for use as ultrasound contrast agent (UCA) and evaluate its effects in ultrasonic imaging on normal rabbit's fiver parenchyma. Methods Perfluorocarbon (PFC)-containing microbubbles (ST68-PFC) were prepared by sonication based on suffactant ( Span 60 and Tween 80). Subsequently, the resulting ST68-PFC microbubbles were coated using oppositely charged polyelectrolytes by microbubble-templated layer-by-layer self-assembly technique via electrostatic interaction. The enhancement effects in ultrasonic imaging on normal rabbit's liver parenchyma were assessed. Results The obtained microbubbles exhibited a narrow size distribution. The polyelectrolytes were successfully assembled onto the surface of ST68-PFC microbubbles. In vivo experiment showed that polyelectrolyte multilayer film coated UCA effectively enhanced the imaging of rabbit's liver parenchyma. Conclusions The novel microbubbles UCA coated with polyelectrolyte multilayer, when enabled more function, has no obvious difference in enhancement effects compared with the pre-modified microbubbles. The polymers with chemically active groups ( such as amino group and carboxyl group) can be used as the outermost layer for attachment of targeting ligands onto microbubbles, allowing selective targeting of the microbubbles to combine with desired sites. 展开更多
关键词 MICROBUBBLES ultrasound contrast agent layer-by-layer self-assembly technique POLYELECTROLYTE
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3D graphene foam-supported cobalt phosphate and borate electrocatalysts for high-efficiency water oxidation 被引量:10
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作者 Min Zeng Hao Wang +3 位作者 Chong Zhao Jiake Wei Wenlong Wang Xuedong Bai 《Science Bulletin》 SCIE EI CAS CSCD 2015年第16期1426-1433,共8页
The cobalt phosphate-/cobalt borate-based oxygen-evolving catalysts (OECs) are the important class of earth-abundant electrocatalysts that can operate with high activity for water splitting under benign conditions. ... The cobalt phosphate-/cobalt borate-based oxygen-evolving catalysts (OECs) are the important class of earth-abundant electrocatalysts that can operate with high activity for water splitting under benign conditions. This article reports the integration of cobalt phosphate (Co- Pi) and cobalt borate (Co-Bi) OECs with three-dimensional (3D) graphene foam (GF) for the electrocatalytic water oxidation reaction. The GF showed a unique advantage to serve as a highly conductive 3D support with large capacity for anchoring and loading Co-OECs, thereby facilitating mass and charge transfer due to the large amount of active sites provided by the 3D graphene scaffold. As a result, this integrated system of GF and Co-OECs exhibits synergistically enhanced catalytic activity. The overpotential (η) of Co-Pi and Co-Bi/graphene catalysts is about 0.390 and 0.315 V in neutral solutions, respectively. Besides, the integrated Co-OECs/graphene catalysts have also exhibited improved and stable oxygen evolution catalytic ability in alkaline solution. 展开更多
关键词 Water splitting Oxygen evolutioncatalyst Cobalt phosphate and borate Graphene foam
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Inactivating SARS-CoV-2 by electrochemical oxidation
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作者 Yunchuan Tu Wei Tang +11 位作者 Liang Yu Zheyi Liu Yanting Liu Huicong Xia Haiwei Zhang Shiyun Chen Jia Wu Xiaoju Cui Jianan Zhang Fangjun Wang Yangbo Hu Dehui Deng 《Science Bulletin》 SCIE EI CSCD 2021年第7期720-726,M0004,共8页
Fully inactivating SARS-Co V-2, the virus causing coronavirus disease 2019, is of key importance for interrupting virus transmission but is currently performed by using biologically or environmentally hazardous disinf... Fully inactivating SARS-Co V-2, the virus causing coronavirus disease 2019, is of key importance for interrupting virus transmission but is currently performed by using biologically or environmentally hazardous disinfectants. Herein, we report an eco-friendly and efficient electrochemical strategy for inactivating the SARS-Co V-2 using in-situ formed nickel oxide hydroxide as anode catalyst and sodium carbonate as electrolyte. At a voltage of 5 V, the SARS-Co V-2 viruses can be rapidly inactivated with disinfection efficiency reaching 95% in only 30 s and 99.99% in 5 min. Mass spectrometry analysis and theoretical calculations indicate that the reactive oxygen species generated on the anode can oxidize the peptide chains and induce cleavage of the peptide backbone of the receptor binding domain of the SARS-Co V-2 spike glycoprotein, and thereby disables the virus. This strategy provides a sustainable and highly efficient approach for the disinfection of the SARS-CoV-2 viruliferous aerosols and wastewater. 展开更多
关键词 Electrochemical oxidation Reactive oxygen specie Receptor binding domain SARS-Co V-2
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