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首页> 外文期刊>Designed Monomers and Polymers >Synthesis, Characterization and Properties of New Fluorinated Poly(imide siloxane) Co-polymers from 4,4′-(Hexafluoro-isopropylidene)diphthalic Anhydride
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Synthesis, Characterization and Properties of New Fluorinated Poly(imide siloxane) Co-polymers from 4,4′-(Hexafluoro-isopropylidene)diphthalic Anhydride

机译:4,4'-(六氟异亚丙基)二苯酐新型氟化聚(酰亚胺硅氧烷)共聚物的合成,表征和性能

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Several new poly(imide siloxane)s co-polymers have been prepared by the reaction of 4,4′-(hexafluoroisopropylidene)diphthalic anhydride (6FDA) with commercially available 4,4′-oxydianiline (ODA) and with five different novel trifluoromethyl-substituted diamines, each with 20 wt% aminopropyl-terminated polydimethylsiloxane (APPS). The poly(imide siloxane)s are well characterized by different spectroscopic, thermal, mechanical and electrical techniques. The synthesized polymers exhibit good solubility in different organic solvents. The ~(1)H-NMR indicates that the siloxane incorporation is about 17–19% for polymers 1a–f. These poly(imide siloxane) films show low water absorption rate (0.88–0.09%) and a low dielectric constant (2.43–2.58) at 1 MHz. The polymers show very good thermal stability, even up to 419°C for 5% weight loss in synthetic air and a glass transition temperature of up to 230°C. All poly(imide siloxane)s formed tough transparent films, with a tensile strength of up to 79 MPa, a modulus of elasticity of up to 1.38 GPa and elongation-at-break of up to 30%. Thermal, mechanical and dielectric properties of these polymers have been evaluated and compared with their non-siloxane analogues.
机译:通过使4,4'-(六氟异亚丙基)二邻苯二甲酸酐(6FDA)与可商购的4,4'-氧基二苯胺(ODA)和五种不同的新型三氟甲基-苯胺反应,制备了几种新型的聚(酰亚胺硅氧烷)共聚物。取代的二胺,每个均含20重量%氨基丙基封端的聚二甲基硅氧烷(APPS)。聚(酰亚胺硅氧烷)通过不同的光谱,热,机械和电技术很好地表征。合成的聚合物在不同的有机溶剂中显示出良好的溶解性。 〜(1)H-NMR表明,聚合物1a-f的硅氧烷掺入量约为17-19%。这些聚(酰亚胺硅氧烷)薄膜在1 MHz时显示出低吸水率(0.88–0.09%)和低介电常数(2.43–2.58)。该聚合物表现出非常好的热稳定性,即使在高达419°C的条件下,在合成空气中的重量损失为5%,玻璃化转变温度也高达230°C。所有聚(酰亚胺硅氧烷)均形成坚韧的透明薄膜,其拉伸强度高达79 MPa,弹性模量高达1.38 GPa,断裂伸长率高达30%。已经评估了这些聚合物的热,机械和介电性能,并与它们的非硅氧烷类似物进行了比较。

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