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RAFT Dispersion Alternating Copolymerization of Styrene with N-Phenylmaleimide: Morphology Control and Application as an Aqueous Foam Stabilizer

机译:苯乙烯与N-苯基马来酰亚胺的RaFT分散交替共聚合:形态控制及作为水性泡沫稳定剂的应用

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摘要

We report a new nonaqueous polymerization-induced self-assembly (PISA) formulation based on the reversible addition−fragmentation chain transfer (RAFT) dispersion alternating copolymerization of styrene with N-phenylmaleimide using a nonionic poly(N,N-dimethylacrylamide) stabilizer in a 50/50 w/w ethanol/methyl ethyl ketone (MEK) mixture. The MEK cosolvent is significantly less toxic than the 1,4-dioxane cosolvent reported previously [Yang, P.; et al. Macromolecules 2013, 46, 8545−8556]. The core-forming alternating copolymer block has a relatively high glass transition temperature (Tg), which leads to vesicular morphologies being observed during PISA, as well as the more typical sphere and worm phases. Each of these copolymer morphologies has been characterized by transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) studies. TEM studies reveal micrometer-sized elliptical particles with internal structure, with SAXS analysis suggesting an oligolamellar vesicle morphology. This structure differs from that previously reported for a closely related PISA formulation utilizing a poly(methacrylic acid) stabilizer block for which unilamellar platelet-like particles are observed by TEM and SAXS. This suggests that interlamellar interactions are governed by the nature of the steric stabilizer layer. Moreover, using the MEK cosolvent also enables access to a unilamellar vesicular morphology, despite the high Tg of the alternating copolymer coreforming block. This was achieved by simply conducting the PISA synthesis at a higher temperature for a longer reaction time (80 °C for 24 h). Presumably, MEK solvates the core-forming block more than the previously utilized 1,4-dioxane cosolvent, which leads to greater chain mobility. Finally, preliminary experiments indicate that the worms are much more efficient stabilizers for aqueous foams than either the spheres or the oligolamellar elliptical vesicles.
机译:我们报告了一种新的非水聚合诱导自组装(PISA)配方,该配方基于苯乙烯与N-苯基马来酰亚胺的可逆加成-断裂链转移(RAFT)分散交替共聚,使用非离子型聚(N,N-二甲基丙烯酰胺)稳定剂。 50/50 w / w乙醇/甲乙酮(MEK)混合物。 MEK助溶剂的毒性明显低于先前报道的1,4-二恶烷助溶剂[Yang,P.;等。高分子2013,46,8545−8556]。形成核的交替共聚物嵌段具有相对较高的玻璃化转变温度(Tg),这导致在PISA期间观察到囊泡形态,以及更典型的球形和蠕虫相。这些共聚物形态中的每一种都已经通过透射电子显微镜(TEM)和小角X射线散射(SAXS)研究进行了表征。 TEM研究显示具有内部结构的微米级椭圆形颗粒,而SAXS分析表明为寡层囊泡形态。该结构不同于先前报道的使用聚(甲基丙烯酸)稳定剂嵌段的密切相关的PISA制剂的结构,对于该PISA制剂,通过TEM和SAXS观察到单层血小板状颗粒。这表明层间相互作用受空间稳定剂层的性质支配。而且,尽管交替共聚物芯形成嵌段的Tg很高,但是使用MEK助溶剂也能够获得单层囊泡形态。这是通过简单地在较高的温度下进行较长时间的反应(80°C,24小时)进行PISA合成而实现的。据推测,与以前使用的1,4-二恶烷助溶剂相比,MEK可以使形成芯的嵌段更多地溶剂化,从而提高了链的流动性。最后,初步实验表明,与球形或寡层椭圆形囊泡相比,蠕虫是水性泡沫的有效稳定剂。

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