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Synthesis and characterization of poly(hydroxylic fluoroacrylate)/mSiO _2 nanocomposite by in situ solution polymerization

机译:原位溶液聚合法合成聚(氟代氟代丙烯酸酯)/ mSiO _2纳米复合材料及其表征

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In this study, vinyl-group modified nanosilicas (mSiO_2) were prepared via sol-gel method using vinyltriethoxysilane (VTES) as modifier first, then the novel poly(hydroxylic fluoroacrylate)/mSiO_2 nanocomposite was successfully synthesized by in situ solution polymerization of mSiO _2 with dodecafluoroheptyl methacrylate (DFHMA), β-hydroxyethyl methacrylate (HEMA), methyl methacrylate (MMA), and butyl acrylate (BA) initiated by 2,2-azobisisobutyronitrile (AIBN) in the co-solvents of ethyl acetate and butyl acetate. The chemical composition and structure of the nanocomposite were characterized by Fourier transform infrared spectrometry (FTIR) and transmission electron microscopy (TEM). TEM observation indicated that mSiO_2 nanoparticles obtained a well dispersion in polymeric matrix. Thermogravimetric analysis (TGA) studies revealed that the temperature corresponding to 50% weight loss of the nanocomposite was improved by 21.5°C with the addition of 2.0 wt % mSiO_2. The synthesized nanocomposites were applied to use with hexamethylene diisocyanate trimer (HDIT) to prepare polyurethane materials. Tensile test revealed that polyurethane material with mSiO_2 content of 2.0 wt % showed an ultimate tensile strength of about 5.19 times higher than that without mSiO2. The polyurethane films displayed surface energy of lower than 25 mN m~(-1) and high light transmittance.
机译:本研究首先以乙烯基三乙氧基硅烷(VTES)为改性剂,通过溶胶-凝胶法制备了乙烯基改性纳米二氧化硅(mSiO_2),然后通过原位溶液聚合mSiO _2成功地合成了新型聚羟基氟丙烯酸酯/ mSiO_2纳米复合材料。与甲基丙烯酸十二氟庚基酯(DFHMA),甲基丙烯酸β-羟乙基酯(HEMA),甲基丙烯酸甲酯(MMA)和丙烯酸丁酯(BA)由2,2-偶氮二异丁腈(AIBN)在乙酸乙酯和乙酸丁酯的共溶剂中引发的反应通过傅立叶变换红外光谱(FTIR)和透射电子显微镜(TEM)表征了纳米复合材料的化学组成和结构。 TEM观察表明,mSiO_2纳米粒子在聚合物基质中具有良好的分散性。热重分析(TGA)研究表明,通过添加2.0 wt%的mSiO_2,与纳米复合材料的50%重量损失相对应的温度提高了21.5°C。将合成的纳米复合材料与六亚甲基二异氰酸酯三聚体(HDIT)一起使用以制备聚氨酯材料。拉伸试验表明,mSiO 2含量为2.0重量%的聚氨酯材料的极限抗拉强度比没有mSiO 2的极限抗拉强度高约5.19倍。聚氨酯薄膜的表面能低于25 mN m〜(-1),透光率高。

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