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Crystallization of alcohol ethoxylate diblock copolymers from body-centred cubic micellar phases formed in concentrated aqueous solutions

机译:醇乙氧基化物二嵌段共聚物从在浓水溶液中形成的体心立方胶束相结晶

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摘要

Crystallization in concentrated aqueous solutions of the alcohol ethoxylate diblock copolymers C11E40, C15E39 and C17E40 (where C = methylene or methyl and E = oxyethylene) has been investigated using small-angle X-ray scattering (SAXS), wide-angle X-ray scattering (WAXS) and rheology. It is shown that the gel phase formed in these materials has body-centred cubic (bcc) symmetry, and that the bcc structure can be macroscopically oriented by large amplitude oscillatory shear. At concentrations above about 55 wt.-% copolymer, crystallization of the poly(oxyethylene) block occurs at low temperatures, and the effect of crystallization from the oriented bcc structure of a 70 wt.-% solution is examined using SAXS/WAXS. Crystallization induces a second phase separation, i.e. the semicrystalline lamellar structure resulting from poly(oxyethylene)-block crystallization is incommensurate with the oriented bce structure, with which it coexists at low temperatures. However, crystallization produces an unoriented lamellar structure. WAXS indicates that the poly(oxyethylene) in the diblock copolymer crystallizes in its usual (helical) form. [References: 41]
机译:使用小角X射线散射(SAXS)和广角X射线散射研究了乙氧基醇二嵌段醇C11E40,C15E39和C17E40在浓水溶液中的结晶(其中C =亚甲基或甲基,E =氧化乙烯) (WAXS)和流变学。结果表明,在这些材料中形成的凝胶相具有以人体为中心的立方(bcc)对称性,并且bcc结构可以通过大振幅振荡剪切宏观地取向。在高于约55重量%的共聚物的浓度下,聚(氧乙烯)嵌段在低温下发生结晶,并且使用SAXS / WAXS检查了从70重量%溶液的定向bcc结构结晶的效果。结晶引起第二相分离,即,由聚(氧乙烯)-嵌段结晶产生的半结晶层状结构与取向的bce结构不相称,在低温下它与之共存。但是,结晶会产生未取向的层状结构。 WAXS表示二嵌段共聚物中的聚(氧乙烯)以其通常的(螺旋)形式结晶。 [参考:41]

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