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Synthesis and characterization of multiresponsive core-shell microgels

机译:多响应核壳微凝胶的合成与表征

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We report the synthesis and characterization of temperature and pH responsive hydrogel particles (microgels) with core-shell morphologies. Core particles composed of cross-linked poly(N-isopropylacrylamide) (p-NIPAm) or poly(NIPAm-co-acrylic acid) (p-NIPAm-AAc) were synthesized via precipitation polymerization and then used as nuclei for subsequent polymerization of p-NIPAm-AAc and p-NIPAm, respectively. The presence of a core-shell morphology was confirmed by transmission electron microscopy (TEM). Thermally initiated volume phase transitions were interrogated via temperature-programmed photon correlation spectroscopy (TP-PCS) as a function of solution pH. The p-NIPAm-AAc core hydrogel displays both a strong temperature and pH dependence on swelling. However, both p-NIPAm-AAc (core)/p-NIPAm (shell) and p-NIPAm (core)/p-NIPAm-AAc shell) particles display a more complex pH dependence than the homogeneous particles. Specifically, a multistep volume phase transition appears when the AAc component becomes highly charged at a high pH. It is apparent from the measured deswelling curves that a portion of the particle swelling behavior is dominated by p-NIPAm, regardless of its location in the particle. However, deswelling behavior that is due to a mixture of p-NIPAm-AAc and p-NIPAm is evident, as well as a regime that is largely attributed top-NIPAm-AAc alone. Small differences in the effect of pH on the two core-shell particles indicate that the influence of p-NIPAm is somewhat greater when it is localized in the shell. [References: 41]
机译:我们报告合成和表征的温度和pH响应水凝胶颗粒(微凝胶)与核-壳形态。通过沉淀聚合合成由交联的聚(N-异丙基丙烯酰胺)(p-NIPAm)或聚(NIPAm-共丙烯酸)(p-NIPAm-AAc)组成的核心颗粒,然后将其用作随后的p聚合的核-NIPAm-AAc和p-NIPAm。通过透射电子显微镜(TEM)证实了核-壳形态的存在。通过温度程序化的光子相关光谱法(TP-PCS)询问热引发的体积相变与溶液pH的关系。 p-NIPAm-AAc核心水凝胶对膨胀显示出强烈的温度和pH依赖性。但是,p-NIPAm-AAc(核)/ p-NIPAm(壳)和p-NIPAm(核)/ p-NIPAm-AAc壳)均比均质颗粒显示更复杂的pH依赖性。具体而言,当AAc组分在高pH值下带高电荷时,会出现多步体积相变。从测得的溶胀曲线可以明显看出,无论颗粒在颗粒中的位置如何,一部分颗粒的溶胀行为都由p-NIPAm决定。然而,由于p-NIPAm-AAc和p-NIPAm的混合物而引起的溶胀行为是显而易见的,而且这种现象也主要归因于top-NIPAm-AAc。 pH对两个核-壳颗粒的影响的微小差异表明,p-NIPAm位于壳中时,其影响更大。 [参考:41]

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