首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >A Neutron Scattering Study of the Structure of Poly(dimethylsiloxane)-Stabilized Poly(methyl methacrylate)(PDMS-PMMA) Latexes in Dodecane
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A Neutron Scattering Study of the Structure of Poly(dimethylsiloxane)-Stabilized Poly(methyl methacrylate)(PDMS-PMMA) Latexes in Dodecane

机译:多癸烷聚(二甲基硅氧烷) - 硼化聚(甲基丙烯酸甲酯)胶乳(PDMS-PMMA)胶乳结构的中子散射研究

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摘要

Hard-sphere particles in nonpolar solvents are an essential tool for colloid scientists. Sterically stabilized poly(methyl methacrylate) (PMMA) particles have long been used as the exemplary hard-sphere system. However, neither the particles themselves nor the poly(12-hydroxystearic acid) (PHSA) stabilizer necessary to prevent aggregation in nonpolar solvents are commercially available. To counter this, several alternatives have been proposed. In recent years, there has been an increased interest in poly(dimethylsiloxane) (PDMS) stabilizers as a commercially available alternative to PHSA, yet the structure of particles made in this way is not as well understood as those produced using PHSA. In this work, we employ small-angle neutron scattering to determine the internal structure of PDMS-stabilized PMMA particles, synthesized with and without an additional crosslinking agent. We report data consistent with a homogeneous PMMA core with a linearly decaying PDMS shell. The thickness of the shell was in excess of 50 nm, thicker than the PHSA layer typically used to stabilize PMMA but consistent with reports of the layer thickness for similar molecular weight PDMS at planar surfaces. We also show that the amount of the hydrogenous material in the particle core of the crosslinked particles notably exceeds the amount of added ethylene glycol dimethacrylate crosslinker, suggesting some entrapment of the PDMS stabilizer in the PMMA matrix.
机译:非极性溶剂中的硬球颗粒是胶体科学家的必备工具。在空间稳定的聚(甲基丙烯酸甲酯)(PMMA)颗粒长期被用作示例性硬球系统。然而,颗粒本身也不是预防非极性溶剂中聚集所需的聚(12-羟基半胱氨酸)(PHSA)稳定剂是可商购的。为了衡量这一点,已经提出了几种替代方案。近年来,对Poly(二甲基硅氧烷)(PDMS)稳定剂的兴趣增加了作为PPSA的市售替代物,但以这种方式制造的颗粒的结构不太理解,因为使用pHSA产生的那些。在这项工作中,我们采用小角度散射来确定PDMS稳定的PMMA颗粒的内部结构,用额外的交联剂合成。我们报告与具有线性衰减PDMS壳的同一性PMMA芯一致的数据。壳体的厚度超过50nm,比通常用于稳定PMMA的PPSA层厚,但与平面表面上类似分子量PDMS的层厚度的报道一致。我们还表明,交联颗粒的颗粒核中的氢化材料的量特别超过添加的乙二醇二甲基丙烯酸酯交联剂的量,表明PDMS稳定剂在PMMA基质中留下了一些夹杂物。

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