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Supercritical Impregnation and in-situ Polymerization Electrically Conductive Fibres

机译:超临界浸渍和原位聚合导电纤维

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This work shows studies on solubility of monomers and oxidants in scCO_2, on mass transport into important engineering polymers, and on in-situ polymerization. By supercritical impregnation and subsequent in-situ polymerization blends are obtained in a thermally gentle manner. Finally obtained data allow developing ecologically and economically justified - green - processes yielding polymeric blends with otherwise unattainable electrical properties such as tuneable electrical conductivity for electrostatic discharge control. On the way to functional textile fabrics three independent process steps were investigated separately in detail: 1) solubility of monomers and oxidants in scCO_2; 2) sorption of CO_2 into polymers / supercritical impregnation into polymers; 3) in-situ polymerization induced by oxidants (soluble ferric oxidants, iodine). Solubility studies were conducted to approach homogeneous impregnation. In case of the more volatile liquid monomers the synthetic method was applied. The solubility of pyrrole and thiophene in scCO_2 follows 'type I' behaviour for binary systems, increasing steadily with density and temperature in the range of some weight-%. Many [0]amorphous and certain semi-crystalline polymers (like PET and PA6 in this study), absorb considerable amounts of CO_2 in the supercritical state and are thus swollen. The polymer chains become more flexible and the glass transition temperature is depressed. By this lubricating effect and additionally by the high diffusivity and zero vapour pressure of supercritical fluids mass transport is significantly increased. Higher mass transport rates lead to more homogeneous solute distribution before equilibrium. Polymers are subjected to the experiments in form of fabrics or fibres. In-situ polymerization speed depends mostly on concentrations of oxidant and dopant as well as on thermodynamic conditions. The composite polypyrrole coated fabrics are characterized by optical- and electron microscopy (with EDS elemental analysis), Wide angle X-ray diffraction, thermo gravimetric analysis and via micro- ATR FT-IR.
机译:这项工作表明在scCO_2单体和氧化剂的溶解度研究,对大众运输到重要的工程聚合物,并在原位聚合。通过超临界浸渍和随后的原位聚合共混物以热温和的方式获得。最终获得的数据允许生态和经济上合理的显影 - 绿 - 过程得到的聚合物共混物与否则无法实现的电性能,例如用于静电放电控制可调的导电性。的道路上的官能织物三个独立的处理步骤进行了详细的调查分别:1)scCO_2单体和氧化剂的溶解度; 2)CO_2的吸附到聚合物/超临界浸渍到聚合物中; 3)在原位聚合由氧化剂(可溶性​​三价氧化剂,碘)诱导。进行了溶解度研究接近均匀浸渍。在更多的挥发性液体单体的情况下涂布的合成方法。吡咯并在scCO_2溶解度噻吩如下'I型的行为对于二元体系,在一些重量 - %的范围内的密度和温度稳定地增加。许多[0]无定形的和某些半结晶聚合物(如PET和PA6在这项研究中),吸收相当大量的CO_2在超临界状态,并因此溶胀。聚合物链变得更加灵活和玻璃化转变温度被压下。通过由高扩散性和超临界流体的质量传递的零蒸汽压此润滑效果,并且另外是显著增加。较高的传质速率导致平衡以前更均匀的溶质元素分布。聚合物进行的实验中在织物或纤维的形式。原位聚合速度主要取决于氧化剂和掺杂剂的浓度以及对热力学条件。复合聚吡咯涂覆的织物是通过光 - 和电子显微镜(与EDS元素分析),广角X射线衍射,热重分析和通过微ATR FT-IR表征。

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