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DEUTERIUM NMR AND RHEOLOGY OF MICROGEL COLLOIDS AT AMBIENT AND HIGH PRESSURE

机译:常压和高压下微胶体的氘核磁共振和流变学

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摘要

Microgel colloids exhibit a polymer collapse transition resulting in a large reduction in colloid size at high temperatures or pressures. Our goal is to obtain a microscopic understanding of the internal structure and microscopic dynamics of microgels by examining the temperature and pressure dependence of the collapse transition. We have conducted a systematic study of how the nature of this collapse transition is affected by crosslink density (Cd). We used deuterium NMR (~2H-NMR) to probe the microscopic dynamics of cross-linked poly-N-isopropylacrylamide (p-nipam) chains, in microgel colloids, as a function of temperature and pressure. Four differently crosslinked microgels colloids were synthesized with deuteron labels on the nipam backbone (d3-nipam). Corresponding macroscopic properties of unlabeled colloids having the same crosslink densities were characterized by dynamic light scattering (DLS) and rheology. Rheological characterization as a function of temperature (T) and particle concentration (c), and for 4 crosslink densities, showed that the microgel viscosity decreases as temperature is increased, and that in the high T/low c regime, there is a collapse of the viscosity as a function of T and c when plotted against volume fraction: this yields a measure of the water content in the particles as function of T. ~2H-NMR spectra of the d3-nipam suspensions for all Cd indicated freely moving chains at low temperature and a nearly immobilized fraction above 35℃. This is consistent with DLS observations of a transition from swollen to collapsed colloids. ~2H-NMR spectra for the dry powder indicated totally immobilized segments in the particle. Nipam segments in the collapse phase of the d3-nipam suspension were more mobile than those in the dry powder. This suggests significant amounts of water in the collapsed phase, a finding consistent with the rheology observations. For the highest two values of Cd, microgel spectra showed the presence of an immobilized fraction of segments even in the swollen phase. Variable pressure NMR (up to 90 MPa) showed a slight increase in transition temperature with pressure for all Cd values studied.
机译:微凝胶胶体表现出聚合物塌陷转变,从而导致在高温或高压下胶体尺寸大大减小。我们的目标是通过检查塌陷转变的温度和压力依赖性来获得对微凝胶内部结构和微观动力学的微观理解。我们已经对这种塌陷过渡的性质如何受到交联密度(Cd)的影响进行了系统的研究。我们使用氘核磁共振(〜2H-NMR)来探测微凝胶胶体中交联的聚N-异丙基丙烯酰胺(p-nipam)链的微观动力学随温度和压力的变化。合成了四种不同的交联的微凝胶胶体,这些胶体在nipam骨架(d3-nipam)上带有氘核标记。具有相同交联密度的未标记胶体的相应宏观特性通过动态光散射(DLS)和流变学表征。流变特性随温度(T)和颗粒浓度(c)的变化而变化,并且对于4种交联密度,表明微凝胶粘度随温度的升高而降低,而在高T /低c态下,凝胶的塌陷相对于体积分数作图时,粘度随T和c的变化:这是颗粒中水分含量随T的变化的度量。所有Cd的d3-nipam悬浮液的〜2H-NMR光谱表明在低温和高于35℃几乎固定的馏分。这与DLS观察到的从胶体肿胀到塌陷的转变是一致的。干粉的〜2 H-NMR谱表明颗粒中完全固定的链段。 d3-nipam悬浮液崩溃阶段的Nipam片段比干粉中的更易移动。这表明在塌陷相中有大量的水,这一发现与流变学观察结果一致。对于最高的两个Cd值,微凝胶光谱显示,即使在溶胀相中,也存在固定的片段片段。对于所有研究的Cd值,可变压力NMR(最高90 MPa)显示随温度的转变温度略有增加。

著录项

  • 来源
    《Association in solution IV》|2017年|88-88|共1页
  • 会议地点 St. Johns(CA)
  • 作者单位

    Department of Physics and Physical Oceanography, Memorial University, St. John's, NL, Canada;

    School of Applied Sciences, KIIT University, Bhubaneswar, India;

    Department of Physics and Physical Oceanography, Memorial University, St. John's, NL, Canada;

    Department of Physics and Physical Oceanography, Memorial University, St. John's, NL, Canada;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Microgels; Colloids; deuterium; NMR; Rheology;

    机译:微凝胶;胶体;氘; NMR;流变学;

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