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In-depth characterization of granular starch-graft-polyester compositions as obtained by in situ polymerization of lactones from the starch surface

机译:通过从淀粉表面原位聚合内酯获得的颗粒状淀粉接枝聚酯组合物的深入表征

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The synthesis of poly(ε-caprolactone) (PCL)-grafted granular starch was carried out either in bulk (without solvent) or in toluene suspension by a two-step procedure. First step relied upon the activation of the hydroxyl groups available at the starch surface by alkylaluminum derivatives like AlEt_3 and removal of non-surface-grafted organo-aluminum active species. The latter species were made free in solution by reaction with the remaining water molecules still contaminating the polymerization medium despite intensive drying of the starch granules. In the second step, ε-caprolactone was polymerized via a coordination-insertion ring-opening polymerization as initiated by the surface-grafted aluminum alkoxide species. The present contribution aims at investigating various parameters such as nature of the alkyl aluminum activator and monomer (δ-valerolactone was studied as well), temperature, concentration, and addition of a solvent (polymerization in toluene suspension), reaction time, and also the experimental procedure used to recover the polyester chains and measure the grafting efficiency. It turns out that, under the studied conditions, dialkylaluminum alkoxides surface-grafted onto the starch granules were more likely generated and promote a fast polymerization reaction with the formation of grafted PCL chains with a molecular weight that can be as high as 225 000 (M_n value) for polymerization carried out in toluene suspension.
机译:聚(ε-己内酯)(PCL)接枝的粒状淀粉的合成可通过两步程序在本体(无溶剂)或甲苯悬浮液中进行。第一步依靠烷基铝衍生物(如AlEt_3)活化淀粉表面可用的羟基,并去除非表面接枝的有机铝活性物质。通过与剩余的水分子反应,使后一种物质在溶液中游离,尽管淀粉颗粒被强烈干燥,但仍然污染聚合介质。第二步,通过表面接枝的烷醇铝物种引发的配位插入开环聚合反应,使ε-己内酯聚合。本贡献旨在研究各种参数,例如烷基铝活化剂和单体的性质(还研究了δ-戊内酯),温度,浓度和溶剂的添加(甲苯悬浮液中的聚合反应),反应时间以及用于回收聚酯链并测量接枝效率的实验程序。结果表明,在所研究的条件下,更容易产生表面接枝到淀粉颗粒上的二烷基铝醇盐,并促进快速聚合反应,形成分子量高达225 000(M_n)的接枝PCL链。在甲苯悬浮液中进行聚合。

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