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Chemical modification of solid surfaces and interfaces and template-assisted fabrication of surface nanostructures.

机译:固体表面和界面的化学改性以及表面纳米结构的模板辅助制造。

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摘要

Chapter One describes the use of supercritical carbon dioxide (scCO 2) as an agent for the conduction of silane chemistry at the buried interfaces between silicon wafers and spin-cast polymer thin films. Above the critical point of CO2, organosilanes react with surface silanols at the SiO2/polystyrene interface to form a monolayer quantitatively. The ability to do chemistry selectively at weak interfaces offers the potential to rehabilitate coatings and composites.; Chapter Two describes the chemical surface modification of nylon 6/6. Several methods were developed for introducing reactive functional groups to nylon 6/6 surfaces using amide-selective reagents at the solid polymer - solution interface. Hydrolysis of nylon 6/6 yields a surface mixture of amine and carboxylic acid groups. Different alkylating agents, including 2-bromoethylamine, allyl bromide, 1,4-dibromobutane and 4-(trifluoromethyl)benzyl bromide were studied. Reaction of the activated amides with 3-glycidoxypropyltriethoxysilane offers a pathway for generating surfaces with silica-like reactivity. The enrichment of nylon 6/6 with amine functional groups greatly enhances the electroless deposition of gold.; Equally important is the ability to generate surface structures at the nanometer scale in a controlled fashion.; Chapter Three and Chapter Four describe the generation of silicon dioxide (SiO2) nanostructures on silicon wafers using both an organosilane monolayer and a block copolymer thin film as templates, respectively. The resulting surfaces exhibit controlled variation of roughness at the nanometer scale. Contact angle analysis indicates that the effect of nanoscale roughness on wettability is important. Nanoporous films generated from asymmetric block copolymers of styrene and methyl methacrylate (P(S-b-MMA)) were used as scaffolds to define an ordered array of nanoscopic reaction vessels. Nanoscopic posts of silicon oxide on silicon wafers were produced within the pores defined by the crosslinked matrix. Reactive ion etching selectively removed the organic matrix, leaving free-standing silicon dioxide posts on silicon wafers.; Chapter Five describes the examination of the adsorption behavior of different proteins (albumin, lysozyme and collagen) toward surfaces that exhibit nanoscale features. (Abstract shortened by UMI.)
机译:第一章介绍了使用超临界二氧化碳(scCO 2 )作为在硅片和旋转浇铸的聚合物薄膜之间的掩埋界面上传导硅烷化学的试剂。在CO 2 的临界点以上,有机硅烷与SiO 2 /聚苯乙烯界面处的表面硅烷醇反应,定量形成单层。在弱界面选择性地进行化学处理的能力提供了修复涂层和复合材料的潜力。第二章介绍了尼龙6/6的化学表面改性。开发了几种在固体聚合物-溶液界面使用酰胺选择试剂将反应性官能团引入尼龙6/6表面的方法。尼龙6/6的水解产生胺和羧酸基团的表面混合物。研究了不同的烷基化剂,包括2-溴乙胺,烯丙基溴,1,4-二溴丁烷和4-(三氟甲基)苄基溴。活化的酰胺与3-环氧丙氧基丙基三乙氧基硅烷的反应为生成具有类似二氧化硅反应性的表面提供了途径。尼龙6/6带有胺官能团的富集大大增强了金的化学沉积。同样重要的是以受控方式产生纳米级表面结构的能力。第三章和第四章分别描述了使用有机硅烷单层和嵌段共聚物薄膜作为模板在硅片上生成二氧化硅(SiO 2 )纳米结构的过程。所得的表面在纳米尺度上显示出受控的粗糙度变化。接触角分析表明,纳米粗糙度对润湿性的影响很重要。由苯乙烯和甲基丙烯酸甲酯(P(S- b -MMA))的不对称嵌段共聚物产生的纳米多孔膜用作支架,以定义有序的纳米反应容器阵列。在由交联基质限定的孔内产生了硅晶片上的氧化硅的纳米级柱。反应离子蚀刻选择性地去除了有机基质,在硅片上留下了独立的二氧化硅柱。第五章介绍了不同蛋白质(白蛋白,溶菌酶和胶原蛋白)对表现出纳米级特征的表面的吸附行为。 (摘要由UMI缩短。)

著录项

  • 作者

    Jia, Xinqiao.;

  • 作者单位

    University of Massachusetts Amherst.;

  • 授予单位 University of Massachusetts Amherst.;
  • 学科 Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 232 p.
  • 总页数 232
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 高分子化学(高聚物) ;
  • 关键词

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