氟硅共聚改性提高聚丙烯酸酯力学和疏水性能的研究

胡月, 李凤艳, 蔚红建, 赵天波

现代化工 ›› 2021, Vol. 41 ›› Issue (2) : 120 -123,129.

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现代化工 ›› 2021, Vol. 41 ›› Issue (2) : 120-123,129. DOI: 10.16606/j.cnki.issn0253-4320.2021.02.023
科研与开发

氟硅共聚改性提高聚丙烯酸酯力学和疏水性能的研究

    胡月, 李凤艳, 蔚红建, 赵天波
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Study on improvement of mechanical and hydrophobic properties of polyacrylate by copolymerization with fluoro-compounds and silicone

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摘要

为改善聚丙烯酸酯表面能高、力学性能较差的缺点,以丙烯酸酯为主要单体,甲基丙烯酸十二氟庚酯、四甲基四乙烯基环四硅氧烷为功能单体,采用核壳乳液聚合法合成了水性聚氟硅丙烯酸酯。结果表明,四甲基四乙烯基环四硅氧烷可有效提高乳液膜的疏水角、断裂伸长率以及硬度;其质量分数为5%时,乳液的平均粒径为166.8 nm,转化率为98.6%;乳液膜的综合性能最好,其吸水率为3.9%,水接触角为131.3°,拉伸强度为2.3 MPa,断裂伸长率为929.7%,硬度为46.6 HA;与氟硅丙烯酸树脂相比,断裂伸长率提高了58.7%,水接触角提高了11.8%。

Abstract

In order to improve the surface energy and mechanical properties of polyacrylate,a water-borne polyfluorosilicone acrylate resin is synthesized through core-shell emulsion polymerization method with acrylate as main monomer,dodecafluoroheptyl methacrylate and tetramethyl tetravinyl cyclotetrasiloxane as functional monomers.Experimental results show that the addition of tetramethyl tetravinyl cyclotetrasiloxane can effectively improve the hydrophobic angle,elongation at break and hardness of the emulsion film.As the content of tetramethyl tetravinyl cyclotetrasiloxane is 5%,the average particle size of the emulsion is 166.8 nm,the conversion rate reaches 98.6%,and the comprehensive performance of the emulsion film will be the best with a water absorption rate of 3.9%,a water contact angle of 131.3°,a tensile strength of 2.3 MPa,an elongation at break of 929.7%,and a hardness of 46.6 HA.Compared with fluorosilicone acrylic resin,the elongation at break increases by 58.7% and the water contact angle increases by 11.8%.

关键词

核壳乳液聚合 / 力学性能 / 疏水性 / 丙烯酸酯 / 氟硅共聚改性

Key words

core-shell emulsion polymerization / mechanical properties / hydrophobicity / acrylate / modification by copolymerization with fluoro-compounds and silicone

Author summay

胡月(1995-),女,硕士研究生,主要从事化学工程研究,18518567072@163.com

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氟硅共聚改性提高聚丙烯酸酯力学和疏水性能的研究[J]. 现代化工, 2021, 41(2): 120-123,129 DOI:10.16606/j.cnki.issn0253-4320.2021.02.023

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