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Selective CaCO3 Formation within Hydrogels

机译:水凝胶中的选择性Caco3形成

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Nature materials with remarkable mechanical properties are often hybrid materials build-on common inorganic salts and a polymer component, like proteins or polysaccharides. Although all ingredients are accessible, the artificial reconstruction of such materials has not been yet succeeded, because defined nanostructures of the natural materials are responsible for their outstanding performance. Nacre is one of those natural CaCO3 composite materials that contain hierarchically ordered metastable crystals, which are responsible for its excellent mechanical properties. Finding the key factors of the nacre-formation and transferring it to an easy accomplishable, artificial system is the way to open this class of materials for technical applications. In order to create nacre-like structures several groups used surface mineralization in a layer-by-layer fashion. These methods often lead to structures close to the natural idol. Unfortunately they are elaborate, which makes it unlikely to obtain materials thicker than several micrometers. To receive access on artificial large-scale biomaterials it seems to be necessary to effectively calcify the bulk of pre-produced polymer networks. While the influences of low-molecular additives and polymers on crystallization of CaCO3 in solution and on surfaces are pretty well investigated, the understanding of the complex growth inside a polymer network is far more complicated. Thereby the interaction of the crystals with the polymer as well as the suppressed convection and the slowed diffusion of reactants play an important role. These limitations usually result in complex, non-classical and kinetic-controlled crystal growth that affords complex morphologies. Corresponding to this, structure and habit of the grown crystals in a polymer matrix can be influenced by changing gels density and composition, temperature of mineralization or concentration of the reactants. Different kinds of natural and synthetic matrix polymers are suitable to grow CaCO3 crystals within.
机译:具有显着机械性能的自然材料通常是杂种材料,其常见的无机盐和聚合物组分,如蛋白质或多糖。虽然所有成分可接近,但这些材料的人工重建尚未成功,因为所定义的天然材料的纳米结构负责它们的出色性能。珍珠酸盐是含有分层有序亚稳态晶体的天然Caco3复合材料之一,负责其优异的机械性能。寻找直立形成的关键因素并将其转移到易于完成的人工系统,是打开这类材料的技术应用。为了产生类似的珍珠液结构,几个基团以逐层方式使用表面矿化。这些方法通常导致靠近天然偶像的结构。不幸的是,它们是详细的,这使得不太可能获得比几微米厚的材料。接收人工大规模生物材料的访问似乎有必要有效地钙化预生产的聚合物网络。虽然低分子添加剂和聚合物对CaCO 3在溶液中的结晶上的影响非常良好地研究,但是对聚合物网络内的复杂生长的理解更复杂。由此,晶体与聚合物的相互作用以及抑制的对流和反应物的速度扩散起着重要作用。这些限制通常导致复杂,非古典和动力控制的晶体生长,其提供复杂的形态。对应于该聚合物基质中生长晶体的结构和习性可以通过改变凝胶密度和组成,矿化的温度或反应物的浓度来影响。不同种类的天然和合成基质聚合物适合于在内部生长CaCO 3晶体。

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