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Poly(fluoroacrylate)s with tunable surface hydrophobicity via radical copolymerization of 2,2,2-trifluoroethyl α-fluoroacrylate and 2-(trifluoromethyl)acrylic acid

机译:通过2,2,2-三氟乙基α-氟丙烯酸酯和2-(三氟甲基)丙烯酸的自由基共聚可调节表面疏水性的聚(氟丙烯酸酯)

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摘要

The synthesis of poly(fluoroacrylate)s with tunable wettability and improved adhesion for potential application as functional coating was achieved via radical copolymerization of 2,2,2-trifluoroethyl α-fluoroacrylate (FATRIFE) with 2-(trifluoromethyl)acrylic acid (MAF), an adhesion-promoting monomer. These copolymerizations, initiated by tert-butyl peroxypivalate at varying the comonomer feed ([FATRIFE]0/[MAF]0) ratios led to a series of poly(FATRIFE-co-MAF) copolymers with different molar compositions in fair to good conversions (32-87%) depending on the MAF feed content. The microstructures of the synthesized poly(FATRIFE-co-MAF) copolymers were determined by 19F NMR spectroscopy. Even at MAF feed contents higher than 50%, MAF incorporations in the copolymers were lower than 50%, since MAF does not undergo any homopolymerization under radical initiation. The reactivity ratios of the (FATRIFE; MAF) monomer pair were also determined (rFATRIFE = 1.65 ± 0.07 and rMAF = 0 at 56°C) evidencing the formation of statistical copolymers. Initiation involving a highly branched perfluorinated radical that released a •CF3 radical enabled to demonstrate the regioselective attack of the latter radical onto the CH2 of FATRIFE. The resulting poly(FATRIFE-co-MAF) copolymers exhibited various glass transition temperatures (Tgs) depending on their compositions. Tg values increased with increasing MAF contents in the copolymer. In addition, their thermal stability (the temperature for 10% weight loss under air, Td10%) increased with increasing FATRIFE content in the copolymer and reached 348 °C (for that containing 93 mol% of FATRIIFE). Finally, high copolymer MAF content led to both a good adhesion onto metal substrates and to improved hydrophilicity, as revealed by the decrease of the water contact angle from 101° (for a reference poly(FATRIFE) copolymer) to 81° (for a copolymer containing 42 mol % of MAF).
机译:通过2,2,2-三氟乙基α-氟丙烯酸酯(FATRIFE)与2-(三氟甲基)丙烯酸(MAF)的自由基共聚,可以合成具有可调节的润湿性和改进的粘合性的聚(氟丙烯酸酯),以用于潜在的功能涂料。 ,一种增粘单体。这些共聚反应是由过氧新戊酸叔丁酯在不同的共聚单体进料([FATRIFE] 0 / [MAF] 0)比率变化下引发的,从而导致一系列具有不同摩尔组成的聚(FATRIFE-co-MAF)共聚物,转化率基本相同( 32-87%),具体取决于MAF饲料的含量。合成的聚(FATRIFE-co-MAF)共聚物的微观结构通过19F NMR光谱测定。即使在MAF进料含量高于50%时,共聚物中MAF的引入也低于50%,因为MAF在自由基引发下不会发生任何均聚。还确定了(FATRIFE; MAF)单体对的反应性比率(在56℃下rFATRIFE = 1.65±0.07和rMAF = 0),证明统计共聚物的形成。涉及高度支化的全氟自由基的引发,该自由基释放了•CF3自由基,从而能够证明后者的自由基对FATRIFE的CH2的区域选择性攻击。所得的聚(FATRIFE-co-MAF)共聚物根据其组成表现出各种玻璃化转变温度(Tg)。 Tg值随共聚物中MAF含量的增加而增加。此外,它们的热稳定性(空气中失重10%的温度,Td10%)随着共聚物中FATRIFE含量的增加而增加,并达到348°C(对于含有93 mol%FATRIIFE的温度)。最后,高共聚物MAF含量导致在金属基材上的良好附着力以及改善的亲水性,这可以通过将水接触角从101°(对于参考聚(FATRIFE)共聚物)降低到81°(对于共聚物)来揭示。含有42 mol%的MAF)。

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