首页> 外文期刊>Metals materials and processes >ADVANCED POLYMERS: INVESTIGATIONS ON THE INFLUENCE OF MOLECULAR DESIGN, STRUCTURAL PARAMETERS, INTERMOLECULAR FORCES AND PROCESS DESIGN ON PROPERTIES
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ADVANCED POLYMERS: INVESTIGATIONS ON THE INFLUENCE OF MOLECULAR DESIGN, STRUCTURAL PARAMETERS, INTERMOLECULAR FORCES AND PROCESS DESIGN ON PROPERTIES

机译:先进聚合物:关于分子设计,结构参数,分子间作用力和工艺设计对性能的影响的研究

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Investigations based on modem methods of molecular level design philosophy for the design of "structure controlled macromolecules' and similar techniques, carried out on both natural and synthetic polymers involving synthetic and structural studies are presented. Simple chemical modifications such as introducing a phosphate group or a bromine atom on natural monomers based on cashewnut shell liquid (CNSL) and rubber teed oil (RSO) or a grafting reaction on natural polymers such as cellulose brought in enormous improvements in properties. Introducing an acrylate group into cardanol followed by emulsion polymerization changed the area of CNSL chemistry for better applications of these polymers in transparent resin for surface coatings. Further explorations on the special structural features of cardanol led to the finding that the phosphoric acid and sulphonic acid derivatives of cardanol possess multiple functions of plasticization, emulsification, protonation and solubilisation for the preparation of melt/solution processable conducting polyaniline. A judicious choice of comonomert which are characterized by the presence of an aliphatic carbon directly attached to the aromatic moiety enabled synthesis of thermotropic terpolyesters having transition temperatures as low as 240 deg C with a nematic phase required for easy processability. The extensive hydrogen bonding can alto generate LC phases by the alignment of the hydrogen bonded layer structures was shown in the case of poly(esteramide)s (PEA) prepared from amido diols (having a diamide link that can involve in extensive hydrogen bonding) whose aliphatic structures are not expected to contribute to LC phase formation. Similarly, certain azobenzene bated tide chain polymers having carboxylic acid groups were also found stabilised due to hydrogen bond formation. These LC polymers are expected to induce ease of processing and improved properties in thermoplastics and initial studies on rheology and processability are quite encouraging.
机译:提出了基于现代分子水平设计哲学方法的研究,旨在对涉及合成和结构研究的天然和合成聚合物进行“结构控制的大分子”和类似技术的设计,并进行简单的化学修饰,例如引入磷酸基或基于腰果壳液(CNSL)和橡胶四油(RSO)的天然单体上的溴原子或对纤维素等天然聚合物的接枝反应极大地改善了性能,将丙烯酸酯基团引入腰果酚中,然后乳液聚合改变了面积CNSL化学的研究,以更好地将这些聚合物用于表面涂料的透明树脂中,进一步探索腰果酚的特殊结构特征导致发现腰果酚的磷酸和磺酸衍生物具有增塑,乳化,质子化和增溶的多种功能为了 制备熔融/溶液可加工的导电聚苯胺。对共聚单体的明智选择,其特征在于直接与芳族部分相连的脂族碳的存在使得能够合成具有低至240℃的转变温度且具有易于加工所需的向列相的热致性三元聚酯。广泛的氢键结合可以通过氢键合层结构的排列生成LC相,这是由酰胺二醇(具有可参与广泛氢键的二酰胺键)制备的聚(酯酰胺)(PEA)预计脂族结构不会有助于LC相的形成。类似地,由于形成氢键,还发现某些具有羧酸基的偶氮苯联结的潮链聚合物是稳定的。预计这些LC聚合物可简化加工过程并改善热塑性塑料的性能,有关流变性和可加工性的初步研究非常令人鼓舞。

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