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Synthesis of chitosan based semi-IPN hydrogels using epichlorohydrine as crosslinker to study the adsorption kinetics of Rhodamine B

机译:以表氯醇为交联剂合成壳聚糖半IPN水凝胶,研究罗丹明B的吸附动力学

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摘要

The present study is focused on the preparation of chitosan (CS)/polyacrylonitrile (PAN) blend and semi-interpenetrating polymer network (sIPN) hydrogel films, and their application to the adsorption of Rhodamine B dye. The CS/PAN blend hydrogel films were prepared by solution casting technique. To prepare sIPN, CS was cross-linked with epichlorohydrin (ECH). The developed CS/PAN blends and sIPN hydrogels were characterized with field emission scanning electron microscope (FESEM) and Fourier transform infrared (FT-IR) spectroscope. The FESEM micrographs showed no phase separation between CS and PAN. The cross-linking of CS in the sIPN was confirmed by FT-IR. The degree of swelling, W-UB water content, and aqueous stabilities of the blends and sIPN hydrogels were examined at room temperature. Blend film (C8/P2) showed highest % degree of swelling (similar to 2,400%), increased % unbound water (W-UB) (52%), and fair degree of aqueous stability. The swelling of the blends decreased not only with an increase in PAN content but also with cross-linking. At the same CS and PAN composition (C8/P2), sIPN hydrogel exhibited a relatively low degree of swelling (similar to 245%), W-UB, and a high degree of aqueous stability. The potential of the optimized hydrogel film as an adsorbent was evaluated. The q(max) value for c-sIPN was much higher compared to C8/P2 blend film. The adsorption kinetics of Rhodamine B (RB) was observed to follow pseudo-second-order equation and the equilibrium adsorption obeyed Langmuir isotherm equation. The kinetics and adsorption isotherm indicated that the mechanism of adsorption is chemical. However, the FTIR spectra after adsorption showed hydrogen bonding.
机译:本研究的重点是壳聚糖(CS)/聚丙烯腈(PAN)共混物和半互穿聚合物网络(sIPN)水凝胶膜的制备及其在罗丹明B染料吸附中的应用。通过溶液流延技术制备CS / PAN共混水凝胶膜。为了制备sIPN,将CS与环氧氯丙烷(ECH)交联。利用场发射扫描电子显微镜(FESEM)和傅立叶变换红外光谱仪(FT-IR)对已开发的CS / PAN共混物和sIPN水凝胶进行了表征。 FESEM显微照片显示CS和PAN​​之间没有相分离。 FTIR证实了sIPN中CS的交联。在室温下检查共混物和sIPN水凝胶的溶胀度,W-UB含水量以及水稳定性。共混膜(C8 / P2)表现出最高的溶胀度(近似于2,400%),未结合水(W-UB)%升高(52%)以及相当程度的水稳定性。共混物的溶胀不仅随着PAN含量的增加而降低,而且随着交联而降低。在相同的CS和PAN​​成分(C8 / P2)下,sIPN水凝胶具有相对较低的溶胀度(类似于245%),W-UB和较高的水稳定性。评价了优化的水凝胶膜作为吸附剂的潜力。与C8 / P2混合膜相比,c-sIPN的q(max)值高得多。观察到罗丹明B(RB)的吸附动力学遵循拟二级方程,平衡吸附遵循Langmuir等温线方程。动力学和吸附等温线表明吸附机理是化学的。但是,吸附后的FTIR光谱显示出氢键。

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