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Synthesis, Characterization, Topographical Modification, and Surface Properties of Copoly(Imide Siloxane)s

机译:共聚(酰亚胺硅氧烷)的合成,表征,形貌修饰和表面性质

摘要

Novel copoly(imide siloxane)s were synthesized from commercially available aminopropyl terminated siloxane oligomers, aromatic dianhydrides, and diamines. This synthetic approach produced copolymers with well-defined siloxane blocks linked with imide units in a random fashion. The copoly(amide acid)s were characterized by solution viscosity and subsequently used to cast thin films followed by thermal imidization in an inert atmosphere. Thin films were characterized using contact angle goniometry, attenuated total reflection Fourier transform infrared spectroscopy, confocal and optical microscopy, and tensile testing. Adhesion of micronsized particles was determined quantitatively using a sonication device. The polydimethylsiloxane (PDMS) moieties lowered the copolymer surface energy due to migration of siloxane moieties to the film s surface, resulting in a notable reduction in particle adhesion. A further reduction in particle adhesion was achieved by introducing topographical features on a scale of several to tens of microns by a laser ablation technique.
机译:由市售的氨基丙基封端的硅氧烷低聚物,芳族二酐和二胺合成了新型共聚(酰亚胺硅氧烷)。这种合成方法生产的共聚物具有定义明确的硅氧烷嵌段,该嵌段与酰亚胺单元无规连接。通过溶液粘度表征共聚(酰胺酸),随后将其用于流延薄膜,随后在惰性气氛中进行热酰亚胺化。使用接触角测角法,衰减全反射傅立叶变换红外光谱,共焦和光学显微镜以及拉伸测试对薄膜进行表征。使用超声处理装置定量测定微粒化颗粒的粘附力。由于硅氧烷部分向膜表面的迁移,聚二甲基硅氧烷(PDMS)部分降低了共聚物的表面能,导致颗粒附着力显着降低。通过采用激光烧蚀技术在几微米到几十微米的尺度上引入形貌特征,可以实现颗粒附着力的进一步降低。

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