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Channel regulation of TFC membrane with hydrophobic carbon dots in forward osmosis
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作者 Zongju Zhang Jiugang Hu +5 位作者 Shijun Liu Xin Hao Lin Li Guoqiang Zou Hongshuai Hou Xiaobo Ji 《Chinese Chemical Letters》 SCIE CAS CSCD 2021年第9期2882-2886,共5页
Zero-dimensional carbon dots have emerged as important nanofillers for the separation membrane due to their small specific size and rich surface functional groups.This study proposed a strategy based on hydrophobic ca... Zero-dimensional carbon dots have emerged as important nanofillers for the separation membrane due to their small specific size and rich surface functional groups.This study proposed a strategy based on hydrophobic carbon dots(HCDs)to regulate water channels for an efficient forward osmosis(FO)membrane.Thin-film composite(TFC)membranes with superior FO performance are fabricated by introducing HCDs as the nanofiller in the polyacrylonitrile support layer.The introduction of HCDs promotes the formation of the support layer with coherent finger-like hierarchical channels and micro-convex structure and an integrated polyamide active layer.Compared to the original membrane,TFC-FO membrane with 10 wt%HCDs exhibits high water flux(15.47 L m^(-2)h^(-1))and low reverse salt flux(2.9 g m^(-2)h^(-1))using 1 mol/L Na Cl as the draw solution.This improved FO performance is attributed to the lower structural parameters of HCDs-induced water channels and alleviated internal concentration polarization.Thus,this paper provides a feasible strategy to design the membrane structure and boost FO performance. 展开更多
关键词 Forward osmosis Thin-film nanocomposite Hydrophobic carbon dots channel regulation NANOFILLERS
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Synthesis and Characterization of A Small Molecule CFTR Chloride Channel Inhibitor 被引量:1
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作者 HECheng-yan ZHANGHeng-jun +3 位作者 SUZhong-min ZHOUJin-song YANGHong MATong-hui 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2004年第3期334-337,共4页
A thiazolidinone CFTR inhibitor(CFTR_ inh-172 ) was synthesized by a three-step procedure with trifluromethylaniline as the starting material. The synthesized CFTR inhibitor was characterized structurally by means of... A thiazolidinone CFTR inhibitor(CFTR_ inh-172 ) was synthesized by a three-step procedure with trifluromethylaniline as the starting material. The synthesized CFTR inhibitor was characterized structurally by means of 1H NMR and functionally in a CFTR-expressing cell line FRT/hCFTR/EYFP-H148Q by both fluorescent and electrophysiological methods. A large amount(100 g) of high-quality small molecule thiazolidinone CFTR chloride channel inhibitor,CFTR_ inh-172 ,can be produced with this simple three-step synthetic procedure. The structure of the final product 2-thioxo-3-(3-trifluromethylphenyl)-5-[4-carboxyphenyl- methylene]-4-thiazolidinone was confirmed by 1H NMR. The overall yield was 58% with a purity over 99% as analyzed by HPLC. The synthesized CFTR_ inh-172 specifically inhibited CFTR chloride channel function in a cell-based fluorescence assay( K _d≈1.5 μmol/L) and in a Ussing chamber-based short-circuit current assay( K _d≈0.2 μmol/L),indicating better quality than that of the commercial combinatorial compound. The synthesized inhibitor is nontoxic to cultured cells at a high concentration and to mouse at a high dose. The synthetic procedure developed here can be used to produce a large amount of the high-quality CFTR_ inh-172 suitable for antidiarrheal studies and for creation of cystic fibrosis models in large animals. The procedure can be used to synthesize radiolabled CFTR_ inh-172 for in vivo pharmacokinetics studies. 展开更多
关键词 Cystic fibrosis transmembrane conductance regulator(CFTR) CFTR chloride channel Fisher rat thyroid(FRT) Yellow fluorescent protein(YFP) Diarrhea Cystic fibrosis
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Impact Analysis of Coastal Engineering Projects on Mangrove Wetland Area Change with Remote Sensing 被引量:4
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作者 李天宏 韩鹏 赵志杰 《China Ocean Engineering》 SCIE EI 2008年第2期347-358,共12页
In the past decades, two large scale coastal engineering projects have been carried out in the Deep Bay surrounded by Shenzhen City and Hong Kong Special Administrative Region. One project is Shenzhen River channel re... In the past decades, two large scale coastal engineering projects have been carried out in the Deep Bay surrounded by Shenzhen City and Hong Kong Special Administrative Region. One project is Shenzhen River channel regulation and the other is the sea reclamation along the seashore on the Shenzhen side. The two projects are very close to the two national nature reserves, specifically Futian in Shenzhen and Mai Po in Hong Kong, which are important wetland ecosystems worldwide. This paper aims to identify and monitor the mangrove wetland changes with time series of Landsat Thematic Mapper images pre and post to the two engineering projects being launched. Coupled analysis of the image interpretation results and tidal data acquired at the same time in the context of the two works reveals that the mangrove wetland area has increased from year 1989 to 1994, and has changed little from year 1994 to 2002. Binary coding is applied to reveal the distribution image of mangrove at each phase, and the coding image shows that the construction of the two coastal engineering projects has caused frequent changes in mangrove spatial distribution. The study also shows that the change is not significant regarding to the precision of the method and the natural evolution of mangrove wetland, and the projects do not cause apparently influences upon the two national mangrove conservation zones at least for the research time period. 展开更多
关键词 mangrove wetland remote sensing sea reclamation river channel regulation the Deep Bay
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Ryanodine receptor-protein regulator interaction revealed a general molecular mechanism of channel inhibition
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作者 Chang-Cheng Yin Department of Biophysics, Health Science Center, Peking University, 38 Xueyuan Road, Beijing 100191, 《生物物理学报》 CAS CSCD 北大核心 2009年第S1期79-79,共1页
Ryanodine receptors (RyR) are the major Ca2+ release channels in both cardiac and skeletal muscle, they play a crucial role in the Ca2+ signaling pathway that govern the
关键词 RyR Ryanodine receptor-protein regulator interaction revealed a general molecular mechanism of channel inhibition
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