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Fractionation of carboxylate anions from aqueous solution using chitosan cross-linked sorbent materials

机译:使用壳聚糖交联吸附材料的水溶液中羧酸块阴离子的分馏

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摘要

The sorptive uptake properties are reported for chitosan and cross-linked chitosan-glutaraldehyde (CG) polymers with single component carboxylic acids (surrogates; Si, i = 1-4). The single component surrogates are treated as model compounds to represent traditional naphthenic acids (NAs) with variable hydrogen deficiency (z) and carbon number (C), as follows: 2-hexyldecanoic acid (z = 0 and C = 16; S1), trans-4-pentylcyclohexanecarboxylic acid (z = -2 and C = 12; S2), dicyclohexylacetic acid (z = -4; C = 14; S3) and 2-ethyl hexanoic acid (z = 0 and C = 8; S4). Cross-linked polymers were synthesized at variable C : G mole ratios (i.e. 1 : 400, 1 : 700, and 1 : 1000) and characterized using FTIR and TGA. The uptake studies were evaluated at pH 6.00 and 9.00 in aqueous solution. Corresponding equilibrium uptake parameters were evaluated by several isotherm models (Sips, Freundlich, and Langmuir). The Freundlich model provided the "best-fit" for S1, S2 and S3. The Sips isotherm model gave the "best-fit" results for S4. The Freundlich sorption affinity constant (K-F; L mg g(-1)) and the Sips monolayer adsorption capacity (Q(m); mg g(-1)) for the sorbent systems was estimated. The parameters for each Si vary as the C : G mole ratio increases (K-F, S1: 0.00800-6.65, S2: 1.41-2.45, S3: 1.29-2.93 and Q(m), S4: 28.4-33.5). Differences in the uptake of Si species by the sorbents were attributed to steric effects between Si with ring systems (z < 0) versus linear alkyl fragments (z = 0). Fractionation of equimolar mixtures of Si reveal that the sorbents display unique and variable binding affinity with remarkable molecular selective uptake (given in parentheses; L mg g(-1)): S1 (4-30) > S2 (4-10) > S3 (3-9). The fractionation efficacy of Si species is attributed to molecular sieving effects due to the tunable micropore sites of the cross-linked polymer, in accordance with the variable cross-linker content of the chitosan framework. Regeneration studies revealed the utility of these materials in cyclic adsorption-desorption processes.
机译:据报道,壳聚糖和交联的壳聚糖 - 戊二醛(Cg)聚合物,用单一组分羧酸(替代物; Si,I = 1-4),报道了吸附吸收性能。单组分替代物被视为模型化合物,以表示具有可变氢缺乏(Z)和碳数(C)的传统环烷酸(NAs),如下:2-己酯(Z = 0和C = 16; S1),反式-4-戊基环己烷基羧酸(Z = -2和C = 12; S2),二环己基乙酸(Z = -4; C = 14; S3)和2-乙基己酸(Z = 0和C = 8; S4) 。交联聚合物在可变C:G摩尔比(即1:400,1:700和1:1000)中合成,并使用FTIR和TGA表征。在水溶液中在pH6.00和9.00中评估摄取研究。通过几个等温模型(SIPS,Freundlich和Langmuir)评估相应的平衡摄取参数。 Freundlich模型为S1,S2和S3提供了“最佳拟合”。 SIPS等温模型为S4提供了“最佳拟合”结果。估计Freundlich吸附亲和力常数(K-F; L mg g(-1))和啜饮单层吸附容量(Q(m); mg g(-1))被用于吸附体系的吸附剂系统。每个Si的参数随着C:G摩尔比增加而变化(K-F,S1:0.00800-6.65,S2:1.41-2.45,S3:1.29-2.93和Q(M),S4:28.4-33.5)。吸附剂对Si物种摄取的差异归因于Si与环系统(Z <0)与线性烷基片段(Z = 0)之间的空间效应。 Si等摩尔混合物的分馏揭示了吸附剂与显着的分子选择性摄取显示独特和可变的结合亲和力(在括号中给出; L Mg G(-1)):S1(4-30)> S2(4-10)> S3 (3-9)。根据壳聚糖框架的可变交联聚合物,Si物种的分馏效应归因于由于交联聚合物的可调谐微孔位点引起的分子筛分作用。再生研究显示了这些材料在循环吸附 - 解吸过程中的效用。

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  • 来源
    《RSC Advances》 |2015年第100期|共13页
  • 作者单位

    Univ Saskatchewan Dept Chem Saskatoon SK S7N 5C9 Canada;

    Univ Saskatchewan Dept Chem Saskatoon SK S7N 5C9 Canada;

    Univ Saskatchewan Dept Chem Saskatoon SK S7N 5C9 Canada;

    Environm Canada Water Sci &

    Technol Directorate Saskatoon SK S7N 3H5 Canada;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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