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Formation of organic-inorganic nano/microcomposites using environmentally benign solvents or processes.

机译:使用对环境无害的溶剂或工艺形成有机-无机纳米/微复合材料。

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This dissertation involves development of organic/inorganic hybrids utilizing supercritical carbon dioxide (s0002), wherein at least one component has a characteristic length scale below 10 mum. One of the systems studied is a block copolymer (BC) comprising CO2-philic (polydimethylsiloxane) and metallated (polyferrocenylsilane) (PFS) blocks. The BC dissolves into the CO2-phase and forms soft nanostructures of varying size, shape and complexity depending on the pressure, temperature and time of exposure. The nanostructures were "harvested" upon depressurization and analyzed via transmission electron microscopy. Systems such as these are of particular relevance to the microelectronics sector, and this work is intended to open new avenues to novel materials that can be used therein.; Another composite system focused not on the CO2-rich phase, but the polymer-rich phase and CO2-induced swelling and plasticization. Thin films of functionalized PFS homopolymer, a ceramic precursor, were exposed to S0002 in a high-pressure batch vessel at varying temperatures and pressures and for differing saturation times. Isotropic microcellular polymeric foams were produced similar to that for commodity polymers like poly(methylmethacrylate) and polystyrene (PS). Additionally, judicious parameter selection produced bimodal distributions of pore cells and anisotropic pore cells termed "V-directional" cells from the neat homopolymer.; The final composite system comprised silicate (clay) platelets that serve as hard fillers with either nano- or micro-size scales depending on the platelet dispersion. Various fabrication techniques and formulations were explored and this dissertation describes a mechanism for producing intercalated or exfoliated nanocomposites (NCs) from an immiscible system. Exposure of the immiscible NC to an oxidative environment (i) breaks up polymer chains bridging the edges of the silicate platelets allowing a less obstructed pathway for intercalation and (ii) induces chain scission near the periphery of the platelets to provide chains of reduced molecular weight that have more favorable intercalation capability. scCO2 treatment of an immiscible NC system may be postulated to increase the diffusion of chains into the clay gallery, change interfacial tensions or swell the interlayer spacing to increase the d-spacing, all of which might promote intercalation. However, our results indicate that scCO2 behaves similar to inert environments like vacuum and nitrogen for our particular system comprising PS and organically-modified montmorillonite (OM-MMT). To better understand our system, an analysis of the individual polymer and clay properties and stability were undertaken. Insight was gained on the limited thermal stability of OM-MMT and the extreme alignment of clay platelets after processing. The latter may help in the development of impermeable membranes when the platelets are aligned with their surface normal parallel to the diffusive direction.
机译:本论文涉及利用超临界二氧化碳(s0002)开发有机/无机杂化体,其中至少一种组分具有低于10μm的特征长度尺度。所研究的系统之一是嵌段共聚物(BC),其包含亲CO2(聚二甲基硅氧烷)和金属化(聚二茂铁基硅烷)(PFS)嵌段。 BC溶解到CO2相中,并形成软纳米结构,其大小,形状和复杂程度取决于压力,温度和暴露时间。减压后“收获”纳米结构并通过透射电子显微镜分析。诸如此类的系统与微电子领域特别相关,这项工作旨在为可以在其中使用的新型材料开辟新的途径。另一个复合系统的重点不是富CO2相,而是富聚合物相和CO2引起的溶胀和塑化。将官能化的PFS均聚物(一种陶瓷前体)薄膜在高压间歇式容器中于变化的温度和压力下以及不同的饱和时间下暴露于S0002。各向同性的微孔聚合物泡沫的生产类似于商品聚合物,如聚甲基丙烯酸甲酯和聚苯乙烯(PS)。另外,明智的参数选择产生了由纯净均聚物制成的孔细胞和各向异性孔细胞的双峰分布,被称为“ V方向”细胞。最终的复合材料系统包含硅酸盐(粘土)薄片,这些薄片可以根据血小板的分散性以纳米或微米级尺度用作硬质填充物。探索了各种制造技术和配方,本论文描述了一种由不混溶系统生产插层或脱落纳米复合材料的机理。将不混溶的NC暴露在氧化环境中(i)破坏桥接硅酸盐血小板边缘的聚合物链,从而减少了插入的障碍,并且(ii)在血小板外围附近引起链断裂,从而提供了分子量降低的链具有更好的插层能力。可以假定对不相容的NC系统进行scCO2处理可增加链向粘土通道中的扩散,改变界面张力或溶胀中间层间距以增加d间距,所有这些都可能促进嵌入。但是,我们的结果表明,对于包含PS和有机改性蒙脱土(OM-MMT)的特定系统,scCO2的行为类似于惰性环境,如真空和氮气。为了更好地了解我们的系统,对单个聚合物和粘土的性能及稳定性进行了分析。对OM-MMT有限的热稳定性和加工后粘土薄片的极端排列获得了见识。当血小板与其表面法线平行于扩散方向排列时,后者可能有助于不渗透膜的形成。

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