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首页> 外文期刊>Journal of Applied Polymer Science >Grafting and Phosphonic Acid Functionalization of Hyperbranched Polyamidoamine Polymer onto Ultrafine Silica
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Grafting and Phosphonic Acid Functionalization of Hyperbranched Polyamidoamine Polymer onto Ultrafine Silica

机译:超支化聚酰胺胺聚合物在超细二氧化硅上的接枝和膦酸官能化

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In this Study, grafting of hyperbranched polyamidoamine (PAMAM) polymer onto Ultrafine silica followed by functionalization via the introduction of phosphonic acid groups into the branch ends was performed. First, an initiating site was incorporated into the silica surface by reacting the silica silanol group with 3-aminopropyltriethoxysilane, producing amino-functionalized silica. The free amine group content was altered by varying the ratio of methanol to water in the hydrolysis step of the silanization reaction. Grafting of PAMAM was attained by three rounds of sequential Michael addition of silica amine groups to methyl acrylate and amidation of the resulting terminal methyl ester groups with ethylenediamine. Completion of the grafting reaction in each step was clearly confirmed using FTIR analysis. Excessive ethylenediamine and unattached hyperbranched PAMAM present in the reaction product were removed by dialysis with a molecular weight cutoff of 6000-7000 Daltons. However, the amino group content determined in each step was found to be significantly lower than theoretically expected, perhaps indicative of side reactions and, in later stages, steric hindrance. The resultant hyperbranched PAMAM-grafted onto silica was functionalized by phosphorylation of the terminal amino groups by a Mannich type reaction, producing the phosphorylated hyperbranched PAMAM-grafted silica. Then its application on cotton fabric to produce fire-retardant cellulose was tentatively investigated. (C) 2008 Wiley Periodicals, Inc. J Appl Polym Sci 110: 3336-3347,2008
机译:在这项研究中,进行了超支化聚酰胺胺(PAMAM)聚合物的接枝到超细二氧化硅上,然后通过将膦酸基团引入分支末端进行功能化。首先,通过使二氧化硅硅烷醇基与3-氨基丙基三乙氧基硅烷反应,将引发位点结合到二氧化硅表面中,从而制备氨基官能化的二氧化硅。通过在硅烷化反应的水解步骤中改变甲醇与水的比例来改变游离胺基含量。 PAMAM的接枝是通过三轮将硅烷基胺基团迈克尔依次加成到丙烯酸甲酯上,然后用乙二胺酰胺化所得的末端甲酯基团来实现的。使用FTIR分析清楚地证实了每个步骤中的接枝反应的完成。通过透析以6000-7000道尔顿的截留分子量除去存在于反应产物中的过量乙二胺和未连接的超支化PAMAM。但是,发现在每个步骤中确定的氨基含量均明显低于理论上的预期值,这可能表明存在副反应,并在以后的阶段表明了位阻。通过曼尼希(Mannich)型反应使末端氨基磷酸化,从而使接枝到二氧化硅上的所得超支化PAMAM官能化,从而生产了磷酸化的超支化PAMAM接枝的二氧化硅。然后初步研究了其在棉织物上生产阻燃纤维素的应用。 (C)2008 Wiley Periodicals,Inc. J Appl Polym Sci 110:3336-3347,2008

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