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Nanogels and microgels: The new polymeric materials playground

机译:纳米凝胶和微凝胶:新型聚合材料领域

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摘要

Microgels, or intramolecularly crosslinked macromolecules (ICMs), have been known for a number of years. They are formed during the polymerization of polyfunctional precursors en-route, but at incomplete reaction, to the macrogelation predicted by the theories of gelation initially propounded by Carothers and Flory. These gelation theories did not predict that such microgels made in solution could be prepared from such polyfunctional reactive solutions at complete reaction and high concentrations, without gelation. Microgels have been successfully and usefully prepared, however, at complete conversion of their contained reactive groups by the use of either aqueous or non-aqueous dispersion polymerization in which surface active agents are utilized to contain the polymerization to isolated submicron-size domains. The progression towards macrogelation is constrained to the maximum size of the dispersed domains. This paper demonstrates the contrasting general observation that macrogelation in solvents of such polyfunctional reactive precursors cannot occur below a Critical Gelation Concentration (CGC) if a carefully selected match of solvent solubility parameters for the polymerization solvent and the formed polymer is made. In some cases the addition of only ca, ten percent w/w of solvent is required to completely prevent macrogelation at complete conversion. In addition polymerization the molecular weight of the produced ICMs may be varied in a simple controllable manner from the low thousands (nanogels) to many millions (microgels) simply by the choice of concentration at which they are prepared. The products are a distinct form of polymer which is quite different to the linear analogue and almost certainly these solution-prepared products are different to the microgels formed by aqueous dispersion polymerization techniques. This new solution technique provides a simple and general new method for the ready synthesis and design of an enormous range of bespoke globular polymers having both fundamental academic interest and potential commercial utility. [References: 10]
机译:微凝胶或分子内交联的大分子(ICM)已经知道很多年了。它们是在多官能前体的途中聚合过程中形成的,但反应不完全,最初是由Carothers和Flory提出的凝胶化理论所预测的。这些凝胶化理论并未预测溶液中制备的这种微凝胶可以由这种多官能反应性溶液在完全反应和高浓度下制备而无需凝胶化。然而,已经通过使用水性或非水性分散聚合反应成功地并且有用地制备了微凝胶,其中所包含的反应性基团通过使用水性或非水性分散聚合而被使用,其中表面活性剂被用于将聚合反应包含到分离的亚微米尺寸的区域中。朝向大凝胶化的进展被限制在分散域的最大尺寸。本文证明了一种对比性的一般性观察,即如果精心选择了聚合溶剂和所形成聚合物的溶剂溶解度参数匹配,则在这种多官能反应性前体的溶剂中,大凝胶化不会在临界凝胶化浓度(CGC)以下发生。在某些情况下,仅需添加约10%w / w的溶剂即可完全防止完全转化时的大凝胶化。另外,仅通过选择制备它们的浓度,所产生的ICM的分子量就可以以简单可控的方式从低几千(纳米凝胶)到几百万(微凝胶)变化。产物是与线性类似物完全不同的聚合物的独特形式,并且几乎可以肯定,这些溶液制备的产物与通过水分散聚合技术形成的微凝胶不同。这项新的解决方案技术提供了一种简单而通用的新方法,可用于合成和设计具有基本学术兴趣和潜在商业用途的各种定制球形聚合物。 [参考:10]

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