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研制了适用做盐水冷冻液和NaCl冷媒的环保型廉价缓蚀荆,在4℃和30℃的1%~25% NaCl加自来水的盐水溶液中,研制缓蚀剂对低碳钢、低碳锰钢和Cr-Mo钢都有良好的防锈能力,并且在pH值4.O~8.5的塔里木河水中,该缓蚀剂均有缓蚀效果,而以在中性河水中效果最好。 相似文献
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Hope Badawy Jér?me Brunellière Marina Veryaskina Guillaume Brotons Sophie Sablé Isabelle Lanneluc Kelly Lambert Pascal Marmey Amy Milsted Teresa Cutright Arnaud Nourry Jean-Luc Mouget Pamela Pasetto 《International journal of molecular sciences》2015,16(3):4392-4415
There has been an intense research effort in the last decades in the field of biofouling prevention as it concerns many aspects of everyday life and causes problems to devices, the environment, and human health. Many different antifouling and antimicrobial materials have been developed to struggle against bacteria and other micro- and macro-organism attachment to different surfaces. However the “miracle solution” has still to be found. The research presented here concerns the synthesis of bio-based polymeric materials and the biological tests that showed their antifouling and, at the same time, antibacterial activity. The raw material used for the coating synthesis was natural rubber. The polyisoprene chains were fragmented to obtain oligomers, which had reactive chemical groups at their chain ends, therefore they could be modified to insert polymerizable and biocidal groups. Films were obtained by radical photopolymerization of the natural rubber derived oligomers and their structure was altered, in order to understand the mechanism of attachment inhibition and to increase the efficiency of the anti-biofouling action. The adhesion of three species of pathogenic bacteria and six strains of marine bacteria was studied. The coatings were able to inhibit bacterial attachment by contact, as it was verified that no detectable leaching of toxic molecules occurred. 相似文献
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生物技术在现代生活中扮演着越来越重要的角色。本文着重分析了"环境敏感型"大分子及大分子体系在特定环境条件下发生的一些特定的物理和化学性质的变化机理以及利用控制大分子构象得到对特定外界因素敏感的大分子或大分子体系。目的是认识"环境敏感型"大分子或大分子体系在生物技术产品的分离纯化上的具体应用。 相似文献
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Jian Li Gangyao Wen Dimitrios Selianitis Stergios Pispas Yu Zhang Hongfei Li 《应用聚合物科学杂志》2024,141(5):e54898
The aggregation behavior of two pH- and temperature-responsive diblock copolymers of poly[di-(ethylene glycol) methyl ether methacrylate]-block-poly[2-(diisopropylamino) ethyl methacrylate] (PDEGMA-b-PDIPAEMA) at the air/water interface and the structures of their Langmuir–Blodgett (LB) films were studied by the Langmuir monolayer technique and atomic force microscopy, respectively. At the air/water interface, PDEGMA-b-PDIPAEMA tends to form the core-shell-corona micellar structure composed of a PDIPAEMA main chain core, an amino ethyl ester shell, and a PDEGMA corona. Under acidic, neutral, and alkaline conditions, PDIPAEMA blocks are completely protonated, partially protonated, and completely non-protonated, respectively, and the protonated amino ethyl ester groups are immersed in water before monolayer compression, whereas PDEGMA coronas are adsorbed at the interface. At pH 3, 7, and 10, the limiting areas (A0) for PDEGMA42%-PDIPAEMA58% (weight percents) and PDEGMA55%-PDIPAEMA45% are 8.2/10.2/14.0 and 6.7/8.3/8.4 nm2, respectively. The A0 values of the former copolymer are larger than those of the latter. This is because the shells in the former copolymer are denser due to the higher polymerization degree of PDIPAEMA blocks, providing greater steric hindrance for PDEGMA coronas and making the latter more extended at the interface. In contrast to other copolymer systems, the effect of temperature on the isotherms of PDEGMA-b-PDIPAEMA is less obvious. 相似文献
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