Department of Post-Graduate Studies & Research in Chemistry, Mangalore University, Mangalagangothri (DK), 574199, Karnataka, India.
Carbohydr Polym. 2013 Sep 12;97(2):530-6. doi: 10.1016/j.carbpol.2013.04.102. Epub 2013 May 13.
Selective modification of chitosan has been achieved by incorporating ethylene-1,2-diamine molecule in a regioselective manner using N-phthaloylchitosan and chloro-6-deoxy N-phthaloylchitosan as precursors. The present modification results in additional nitrogen centres which function as potential binding sites during adsorption of metal ions. The derivative ethylene-1,2-diamine-6-deoxy-chitosan and its pthaloylated precursor have been evaluated for divalent metal ion removal. The former is found to have higher capacity for adsorption due to the presence of additional NH₂ group. The samples exhibited highest affinity for Cu and least for Zn. About 80% of the adsorbed metal ions could be stripped in a solution of pH 1.2. The interaction between acidic metal centres and basic nitrogen centres on surface of the adsorbent appears to govern adsorption. Intrachain and interchain co-ordinate bonding involving NH and NH₂ groups is proposed to be the mechanism of formation of metal-adsorbent complex. The adsorption process is described by Langmuir model.
采用 N-邻苯二甲酰壳聚糖和氯-6-去氧 N-邻苯二甲酰壳聚糖为前体,以区域选择性的方式将乙二胺分子掺入壳聚糖中,实现了壳聚糖的选择性修饰。这种修饰方法产生了额外的氮中心,这些氮中心在吸附金属离子时可作为潜在的结合位点。对乙二胺-6-去氧壳聚糖及其邻苯二甲酰化前体进行了二价金属离子去除评估。由于存在额外的 NH₂ 基团,前者的吸附能力更高。该样品对 Cu 的亲和力最高,对 Zn 的亲和力最低。在 pH 值为 1.2 的溶液中,约 80%的吸附金属离子可以被洗脱。吸附剂表面上酸性金属中心和碱性氮中心之间的相互作用似乎控制着吸附。提出了涉及 NH 和 NH₂ 基团的链内和链间配位键合是形成金属-吸附剂配合物的机制。吸附过程可用 Langmuir 模型描述。