首页> 外文期刊>Journal of Macromolecular Science. Pure and Applied Chemistry >Grafting of branched polymers onto carbon black surface: Radical postpolymerization initiated by pendant azo groups of grafted polymer on the surface
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Grafting of branched polymers onto carbon black surface: Radical postpolymerization initiated by pendant azo groups of grafted polymer on the surface

机译:支链聚合物接枝到炭黑表面上:自由基接枝聚合是由表面接枝聚合物的侧基偶氮基引发的

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The grafting of highly branched polymer onto carbon black surface by postpolymerization of glycidyl methacrylate (GMA) initiated by pendant azo groups introduced to grafted polyGMA on the surface was investigated. The graft polymerization of GMA onto carbon black was achieved by use of azo groups introduced onto the surface: the percentage of grafting (the proportion of grafted polymer to carbon black) and surface density of grafted polymer to carbon black were determined to be 35.4% and 0.39 mg/m(2), respectively. The introduction of pendant azo groups to grafted polyGMA chain on carbon black was successfully achieved by the reaction of pendant glycidyl groups with 4,4'-azobis(4-cyanopentanoic acid) using (alpha-picolin as a catalyst: the amount of pendant azo groups was determined to be 0.23 mmol/g. It was found that the postpolymerization of GMA was initiated by the pendant azo groups of polyGMA-grafted carbon black and branched polymer was grafted onto carbon black surface: the total grafting of polyGMA was increased from 35.4% (0.39 mg/m(2)) to 47.5% (0.52 mg/m(2)) after the postpolymerization. By repeating the above procedure, i.e., introduction of pendant azo groups and and postpolymerization, highly branched polymers were grafted onto carbon black surface. Branched polymer-grafted carbon black gave a stable colloidal dispersion in good solvents for grafted polymer.
机译:研究了高支化聚合物通过甲基丙烯酸缩水甘油酯(GMA)的后聚合反应,将其接枝到炭黑表面上,该反应由引入到表面接枝的聚GMA上的偶氮侧基引发。通过使用引入到表面的偶氮基团,将GMA接枝到炭黑上:接枝百分比(接枝聚合物与炭黑的比例)和接枝聚合物与炭黑的表面密度分别确定为35.4%和0.39 mg / m(2)。通过将侧链缩水甘油基与4,4'-偶氮双(4-氰基戊酸)(使用α-吡啶啉作催化剂)反应,成功地将侧基偶氮基引入到炭黑上的接枝polyGMA链上测定的基团为0.23mmol / g,发现GMA的后聚合是由聚GMA接枝的炭黑的侧基偶氮基团引发的,并且支链聚合物被接枝到炭黑表面上:polyGMA的总接枝从35.4增加(0.39 mg / m(2))-47.5%(0.52 mg / m(2))通过重复上述步骤,即引入侧基偶氮基团和后聚合,将高度支化的聚合物接枝到碳上支链聚合物接枝的炭黑在接枝聚合物的良好溶剂中具有稳定的胶体分散性。

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