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Synthesis and self-assembly of well-defined binary graft copolymer and its use in superhydrophobic cotton fabrics preparation

机译:明确定义的二元接枝共聚物的合成,自组装及其在超疏水棉织物制备中的应用

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We have synthesized and characterized a series of functional binary graft copolymers PGMA-g-(PHFBMA-r-POEGMA) s(BGCs). First, PHFBMA-C CH, POEGMA-C CH and P(GMA-N-3) were synthesized via sequential atom transfer radical polymerization (ATRP). BGCs were prepared by grafting of alkyne-end poly(hexafluorobutyl methacrylate) (PHFBMA-C CH) and poly(oligo (ethylene glycol) methyl ether methacrylate) (POEGMA-C CH) onto poly(3-azide-2-hydroxypropyl methacrylate) (P(GMA-N-3)) via click chemistry. The self-assembly behaviors were investigated by combination of dynamic light scattering (DLS), transmission electron microscopy (TEM), and atomic force microscopy (AFM). Since POEGMA was soluble in water while PHFBMA was insoluble, BGCs self-assembled and produced stable PHFBMA-centered nano-micelles; then BGCs were used to fabricate hydrophobic cotton fabrics. While the PHFBMA block provided low surface free energy, the POEGMA block served as an anchor with cotton fibers, the modified cotton fabrics showed excellent superhydrophobic property. The results confirmed that fluorinated surface was formed onto substrate without changing the transparency and bulk composition of the cotton fabrics. Moreover, SEM and AFM analysis indicated that nano- and microscale roughness were created by combining BGC-based nano bumps onto surfaces of micro-sized cotton fabrics.
机译:我们已经合成并表征了一系列功能性二元接枝共聚物PGMA-g-(PHFBMA-r-POEGMA)s(BGCs)。首先,通过顺序原子转移自由基聚合(ATRP)合成了PHFBMA-C CH,POEGMA-C CH和P(GMA-N-3)。通过将炔基末端的聚甲基丙烯酸六氟丁酯(PHFBMA-C CH)和聚(低聚乙二醇乙二醇甲基醚甲基丙烯酸酯)(POEGMA-C CH)接枝到聚(3-叠氮化物-2-甲基丙烯酸羟丙酯)上来制备BGC。 (P(GMA-N-3))通过点击化学。通过动态光散射(DLS),透射电子显微镜(TEM)和原子力显微镜(AFM)的组合研究了自组装行为。由于POEGMA可溶于水而PHFBMA不溶于水,因此BGC自组装并产生稳定的以PHFBMA为中心的纳米胶束。然后使用BGC制作疏水棉织物。虽然PHFBMA块提供了低的表面自由能,但POEGMA块充当了棉纤维的锚点,而改性棉织物却表现出出色的超疏水性。结果证实氟化表面形成在基材上,而没有改变棉织物的透明度和膨松组成。此外,SEM和AFM分析表明,通过将基于BGC的纳米凸点结合到微尺寸棉织物的表面上,可以形成纳米级和微米级的粗糙度。

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