کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
232540 465291 2014 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Adsorption kinetics, isotherms and mechanisms of Cd(II), Pb(II), Co(II) and Ni(II) by a modified magnetic polyacrylamide microcomposite adsorbent
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
Adsorption kinetics, isotherms and mechanisms of Cd(II), Pb(II), Co(II) and Ni(II) by a modified magnetic polyacrylamide microcomposite adsorbent
چکیده انگلیسی


• A magnetic hydroxamic acid modified polyacrylamide/Fe3O4 adsorbent was prepared.
• The prepared adsorbent is effective and recyclable for heavy metals.
• Adsorption fit well with pseudo-second order model and Sips isotherm model.
• Pb(II) could be preferentially adsorbed from multi-metal systems.
• The adsorption mechanism was validated by FTIR measurement and DFT calculation.

A novel magnetic hydroxamic acid modified polyacrylamide/Fe3O4 adsorbent (M-PAM-HA) was prepared with acrylamide by microemulsion polymerization and then nucleophilic substitution of hydroxamic acid. The morphology, structure of the magnetic adsorbents before (M-PAM) and after modification (M-PAM-HA) were characterized and their adsorption properties for the removal of metal ions by varying test conditions were also investigated. The modified M-PAM exhibited lower swelling property and less magnetic leaching than M-PAM. Their adsorption kinetics followed the pseudo-second order model. The maximum adsorption capacities of metal ions ranged from 0.11 to 0.29 mmol g−1 for M-PAM and 0.88–1.93 mmol g−1 for M-PAM-HA, respectively. Sips model fitting well to experimental data revealed the surface heterogeneity of the prepared adsorbents. In multi-metal systems, M-PAM-HA showed the relative selectivity toward Pb(II), although Pb(II) was adsorbed the least in their corresponding one-metal systems. The adsorption mechanism was proposed based on the results of FTIR and density functional theory (DFT) calculation.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Water Process Engineering - Volume 4, December 2014, Pages 47–57
نویسندگان
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