席夫碱螯合树脂的比较研究:合成、重金属离子的吸收和热研究

Fatma Al-Yusufy, Mohammed Q. Al-Qadasy, Y. Jamil, Hussein Al-Maydama, Moathe M. Akeel
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引用次数: 6

摘要

用肉桂醛(ci)与邻氨基苯甲酸(aa)和1,4-苯二胺(pn)缩合反应得到的席夫碱自由基共聚制备了两种具有不同组份和不同交联度的螯合树脂Rciaa91和Rciaa73。通过CHN分析、FTIR、1H-NMR和热分析(TGA, DTA)对合成材料进行了表征。采用间歇处理技术,考察了金属离子接触时间、pH和初始浓度对吸附行为的影响。结果表明,在相同条件下,螯合基团组成比例较大、交联程度较低的螯合树脂对Cu(II)、Cd(II)、Co(II)、Zn(II)、Hg(II)、Pb(II)等金属离子的最佳反应时间较短,吸附亲和力较高。两种螯合树脂在最佳pH值、相同反应时间和离子浓度下均表现出对金属离子的吸附行为:Hg2+ > Cu2+ > Zn2+>Pb2+>Co2+ > Cd2+每种金属。采用非等温热重分析(TGA/DTG/DTA),在10℃min-1加热速率和氮气条件下研究了树脂的热降解行为和稳定性。采用Coats-Redfern方法对450-660°C范围内TGA曲线上主要降解步骤的动力学和热力学参数(ΔG*, ΔH*和ΔS*)进行了评价。
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A comparative study of Schiff base chelating resins: synthesis, uptake of heavy metal ions, and thermal studies
Two new chelating resins (Rciaa91 and Rciaa73) with different compositional chelating groups and degree of cross-linking were prepared by free radical copolymerization of Schiff bases obtained from condensation reaction of cinnamaldehyde (ci) with anthranilic acid (aa) and 1,4-phenylenediamine (pn) monomers. The synthesized materials were characterized using CHN analyses, FTIR, 1H-NMR, and thermal analyses (TGA, DTA). Batch technique was applied, and the contact time, pH and initial concentration of the metal ions were investigated as factors affecting the uptake behavior. The results obtained indicated that the chelating resin with larger compositional ratio of chelating moieties and lower degree of cross-linking showed lower optimum reaction time and higher uptake affinity towards the metal ions Cu(II), Cd(II), Co(II), Zn(II), Hg(II), and Pb(II), under the same conditions. Both the chelating resins showed uptake behavior of the metal ions in the following order Hg2+ > Cu2+ > Zn2+>Pb2+>Co2+ > Cd2+ each metal at its optimum pH and at the same reaction time and ion concentration. The thermal degradation behavior and stability of the resins were investigated by using non-isothermal thermogravimetric analysis (TGA/DTG/DTA), at 10 °C min-1 heating rate and under nitrogen. The Coats-Redfern method was used to evaluate the kinetic and thermodynamic parameters (ΔG*, ΔH* and ΔS*) for the prominent degradation steps in the TGA curves at 450-660 °C range.
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