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首页> 外文期刊>ACS Sustainable Chemistry & Engineering >Cellulose, Chitosan and Keratin Composite Materials: Facile and Recyclable Synthesis, Conformation and Properties
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Cellulose, Chitosan and Keratin Composite Materials: Facile and Recyclable Synthesis, Conformation and Properties

机译:纤维素,壳聚糖和角蛋白复合材料:易于回收的合成,构型和性能

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摘要

A method was developed in which cellulose (CEL) and/or chitosan (CS) were added to keratin (KER) to enable [CEL/CS+KER] composites formed to have better mechanical strength and wider utilization. Butylmethylimmidazolium chloride ([BMIm~+Cl~-]), an ionic liquid, was used as the sole solvent, and because the majority of [BMIm~+Cl~-] used (at least 88%) was recovered, the method is green and recyclable. FTIR, XRD, ~(13)C CP- MAS NMR and SEM results confirm that KER, CS and CEL remain chemically intact and distributed homogeneously in the composites. We successfully demonstrate that the widely used method based on the deconvolution of the FTIR bands of amide bonds to determine secondary structure of proteins is relatively subjective as the conformation obtained is strongly dependent on the choice of parameters selected for curve fitting. A new method, based on the partial least squares regression analysis (PLSR) of the amide bands, was developed, and proven to be objective and can provide more accurate information. Results obtained with this method agree well with those by XRD, namely they indicate that although KER retains its second structure when incorporated into the [CEL+CS] composites, it has relatively lower α-helix, higher β-turn and random form compared to that of the KER in native wool. It seems that during dissolution by [BMIm~+Cl~-], the inter- and intramolecular forces in KER were broken thereby destroying its secondary structure. During regeneration, these interactions were reestablished to reform partially the secondary structure. However, in the presence of either CEL or CS, the chains seem to prefer the extended form thereby hindering reformation of the α-helix. Consequently, the KER in these matrices may adopt structures with lower content of a-helix and higher β-sheet. As anticipated, results of tensile strength and TGA confirm that adding CEL or CS into KER substantially increase the mechanical strength and thermal stability of the [CS/CEL+KER] composites.
机译:开发了一种将纤维素(CEL)和/或壳聚糖(CS)添加到角蛋白(KER)中的方法,以使形成的[CEL / CS + KER]复合材料具有更好的机械强度和更广泛的用途。离子液体氯化丁基甲基咪唑鎓盐([BMIm〜+ Cl〜-])用作唯一溶剂,由于回收了大部分[BMIm〜+ Cl〜-](至少88%),因​​此该方法是绿色且可回收。 FTIR,XRD,〜(13)C CP-MAS NMR和SEM结果证实KER,CS和CEL在化学上保持完好无损并均匀分布在复合材料中。我们成功地证明,基于酰胺键的FTIR带反卷积来确定蛋白质的二级结构的广泛使用的方法相对主观,因为获得的构象强烈取决于为曲线拟合选择的参数的选择。基于酰胺带的偏最小二乘回归分析(PLSR),开发了一种新方法,并被证明是客观的,可以提供更准确的信息。用这种方法获得的结果与XRD的结果非常吻合,即它们表明,尽管KER掺入[CEL + CS]复合材料中时仍保留其第二结构,但与-相比,它具有相对较低的α-螺旋,较高的β-转角和无规形式。 KER的天然羊毛。似乎在[BMIm〜+ Cl〜-]溶解过程中,KER中的分子间和分子内力被破坏,从而破坏了其二级结构。在再生过程中,重新建立了这些相互作用,以部分改造二级结构。然而,在存在CEL或CS的情况下,链似乎更喜欢延伸形式,从而阻碍了α-螺旋的重整。因此,这些基质中的KER可能采用a-螺旋含量较低和β-sheet较高的结构。如预期的那样,抗张强度和TGA的结果证实了在KER中添加CEL或CS可以显着提高[CS / CEL + KER]复合材料的机械强度和热稳定性。

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