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首页> 外文期刊>Macromolecules >Thermoresponsive Copolymer Hydrogels on the Basis of N-Isopropylacrylamide and a Non-Ionic Surfactant Monomer: Swelling Behavior, Transparency and Rheological Properties
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Thermoresponsive Copolymer Hydrogels on the Basis of N-Isopropylacrylamide and a Non-Ionic Surfactant Monomer: Swelling Behavior, Transparency and Rheological Properties

机译:基于N-异丙基丙烯酰胺和非离子表面活性剂单体的热敏共聚物水凝胶:溶胀行为,透明度和流变特性

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Copolymer hydrogels were prepared upon γ-ray-induced polymerization of aqueous micellar solutions containing N-isopropylacrylamide (NiPAAm) and the surfactant monomer (surfmer) ω-methoxy poly(ethylene oxide)40undecyl-α-methacrylate (PEO-R-MA-40). Stable, transparent, and thermosensitive hydrogels were obtained in a one-step process. Dose versus conversion measurements showed a complete conversion of comonomer solutions to hydrogels. The size of the surfmer micelles prior and subsequent to polymerization was studied using SAXS measurements. Presence of NiPAAm in the aqueous phase did not influence the size of the PEO-R-MA-40 micelles. During the polymerization process the particle diameter decreased from 7.0 to 5.6 nm probably due to cross-linking in the shell of the micelles. The thermosensitive behavior of the copolymer gels was investigated. The lower critical solution temperature (LCST) of the surfmer-containing gels was higher than for pure poly-NiPAAm (P-NiPAAm) gels, the increase being a direct function of the surfmer concentration. For hydrogels containing small amounts of surfmer, the shrinking at temperatures above the LCST was increased, and the swelling behavior at temperatures below the LCST was slightly increased. The mechanical stability of the copolymer hydrogels was studied using elongational deformation measurements. Presence of surfmer increased the mechanical stability of the hydrogels, the true stress at break being clearly higher for the copolymer gels compared with pure P-NiPAAm gels. A hydrogel containing only 1% (w/w) of surfmer can be elongated up to a true stress being nearly twice as large as for the pure P-NiPAAm gel. This can be explained by the presence of copolymerized micellar aggregates acting as new, stable cross-linking units. A structure model correlating the mechanical properties with a possible network structure is presented.
机译:共聚物水凝胶是通过γ射线诱导的含N-异丙基丙烯酰胺(NiPAAm)和表面活性剂单体(表面活性剂)ω-甲氧基聚(环氧乙烷)40十一烷基-α-甲基丙烯酸酯(PEO-R-MA-40)的胶束水溶液聚合而制备的)。一步法即可获得稳定,透明和热敏的水凝胶。剂量与转化率的测量结果表明共聚单体溶液已完全转化为水凝胶。使用SAXS测量研究了聚合前后的冲浪胶束的尺寸。 NiPAAm在水相中的存在不会影响PEO-R-MA-40胶束的大小。在聚合过程中,粒径可能从7.0 nm减小到5.6 nm,这可能是由于胶束壳中的交联所致。研究了共聚物凝胶的热敏性能。含冲浪剂的凝胶的最低临界溶液温度(LCST)高于纯聚NiPAAm(P-NiPAAm)的凝胶,其升高是冲浪剂浓度的直接函数。对于含有少量冲浪剂的水凝胶,在高于LCST的温度下的收缩增加,而在低于LCST的温度下的溶胀行为略有增加。使用伸长变形测量来研究共聚物水凝胶的机械稳定性。表面活性剂的存在增加了水凝胶的机械稳定性,与纯P-NiPAAm凝胶相比,共聚物凝胶的真正断裂应力明显更高。仅含1%(w / w)的表面活性剂的水凝胶可以拉长到真正的应力,几乎是纯P-NiPAAm凝胶的两倍。这可以通过共聚的胶束聚集体作为新的,稳定的交联单元来解释。提出了一种将机械性能与可能的网络结构相关联的结构模型。

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