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Hydrophobic modification of bagasse cellulose fibers with cationic latex: Adsorption kinetics and mechanism

机译:阳离子乳胶对蔗渣纤维素纤维的疏水改性:吸附动力学和机理

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The modification of the bagasse cellulose fiber by the adsorption of cationic poly latex with core shell structure on fiber surfaces was conducted in attempt to enhance the interfacial compatibility between hydrophilic fibers and the hydrophobic substrates for various applications. A two-step semi-batch emulsion polymerization was employed for constructing core shell latex. TEM and dynamic light scattering (DLS) analysis indicated that the core shell latex possessed a broad particles size distribution, which led to the adsorption of the latex on fiber proceeding via two-stage equilibrium mainly due to the effect of latex particle size. The pseudo-first-order kinetic model was appropriate for the description of the kinetics of the first stage equilibrium at high latex concentration and the entire adsorption process at low concentration. In contrast, the pseudo-second-order kinetic model fitted the second equilibrium at high latex concentration well. The activation energy calculated suggested that the number of activated molecules was increased as the increase of adsorbent concentration, which might change the dominant adsorption mechanism. This also addressed the reasons for the abnormal adsorption behavior with the extra-added emulsifier. In addition, the surface property of the modified cellulose fibers was also investigated via contact angle measurements. The results proved that the cellulose fiber modified with the latex became hydrophobic, allowing the as-modified cellulose to be potential reinforcements for biocomposite. Finally, the adsorption mechanism was proposed according to the adsorption process mainly governed by electrostatic interactions, hydrogen bond, pi-pi stack and chain entanglement. (C) 2016 Elsevier B.V. All rights reserved.
机译:尝试通过在纤维表面上吸附具有核壳结构的阳离子聚乳胶对甘蔗渣纤维素纤维进行改性,以尝试增强亲水纤维与疏水性底物之间的界面相容性,以用于各种应用。采用两步半间歇乳液聚合法制备核壳胶乳。 TEM和动态光散射(DLS)分析表明,核壳胶乳具有较宽的粒径分布,这主要是由于胶乳粒径的影响,导致胶乳通过两步平衡吸附在纤维上。拟一级动力学模型适用于描述高胶乳浓度下的第一阶段平衡动力学和低浓度胶乳下的整个吸附过程。相比之下,伪二级动力学模型很好地拟合了高胶乳浓度下的第二平衡。计算出的活化能表明,随着吸附剂浓度的增加,活化分子的数量增加,这可能会改变主要的吸附机理。这也解决了添加乳化剂导致吸附行为异常的原因。另外,还通过接触角测量研究了改性纤维素纤维的表面性质。结果证明,用乳胶改性的纤维素纤维变为疏水性的,从而使改性后的纤维素成为生物复合材料的潜在增强剂。最后,根据主要受静电相互作用,氢键,π-π堆积和链缠结的吸附过程,提出了吸附机理。 (C)2016 Elsevier B.V.保留所有权利。

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