Synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch

A new chelating ion-exchange resin containing the hydroxamic acid functional group was synthesized from poly(methyl acrylate) (PMA)-grafted sago starch. The PMA grafted copolymer was obtained by a free-radical initiating process in which ceric ammonium nitrate was used as an initiator. Conversion of...

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Main Authors: Lutfor, M. R., Sidik, S., Wan Yunus, W. M. Z., Rahman, M. Z. A., Mansor, A., Haron, M. J.
Format: Article
Language:English
Published: John Wiley & Sons 2001
Online Access:http://psasir.upm.edu.my/id/eprint/114592/
http://psasir.upm.edu.my/id/eprint/114592/1/114592.pdf
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author Lutfor, M. R.
Sidik, S.
Wan Yunus, W. M. Z.
Rahman, M. Z. A.
Mansor, A.
Haron, M. J.
author_facet Lutfor, M. R.
Sidik, S.
Wan Yunus, W. M. Z.
Rahman, M. Z. A.
Mansor, A.
Haron, M. J.
author_sort Lutfor, M. R.
building UPM Institutional Repository
collection Online Access
description A new chelating ion-exchange resin containing the hydroxamic acid functional group was synthesized from poly(methyl acrylate) (PMA)-grafted sago starch. The PMA grafted copolymer was obtained by a free-radical initiating process in which ceric ammonium nitrate was used as an initiator. Conversion of the ester groups of the PMA-grafted copolymer into hydroxamic acid was carried out by treatment of an ester with hydroxylamine in an alkaline solution. The characterization of the poly(hydroxamic acid) chelating resin was performed by FTIR spectroscopy, TG, and DSC analyses. The hydroxamic acid functional group was identified by infrared spectroscopy. The chelating behavior of the prepared resin toward some metal ions was investigated using a batch technique. The binding capacities of copper, iron, chromium, and nickel were excellent and the copper capacity was maximum (3.46 mmol g-1) at pH 6. The rate of exchange of the copper ion was very fast that is, t1/2<5 min. It was also observed that the metal ion-sorption capacities of the resin were pH-dependent and its selectivity toward the metal ions used is in the following order: Cu2+>Fe3+ >Cr3+>Ni2+>Co2+>Zn2+ >Cd2+>As3+>Pb2+.
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publisher John Wiley & Sons
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spelling upm-1145922025-03-05T01:23:15Z http://psasir.upm.edu.my/id/eprint/114592/ Synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch Lutfor, M. R. Sidik, S. Wan Yunus, W. M. Z. Rahman, M. Z. A. Mansor, A. Haron, M. J. A new chelating ion-exchange resin containing the hydroxamic acid functional group was synthesized from poly(methyl acrylate) (PMA)-grafted sago starch. The PMA grafted copolymer was obtained by a free-radical initiating process in which ceric ammonium nitrate was used as an initiator. Conversion of the ester groups of the PMA-grafted copolymer into hydroxamic acid was carried out by treatment of an ester with hydroxylamine in an alkaline solution. The characterization of the poly(hydroxamic acid) chelating resin was performed by FTIR spectroscopy, TG, and DSC analyses. The hydroxamic acid functional group was identified by infrared spectroscopy. The chelating behavior of the prepared resin toward some metal ions was investigated using a batch technique. The binding capacities of copper, iron, chromium, and nickel were excellent and the copper capacity was maximum (3.46 mmol g-1) at pH 6. The rate of exchange of the copper ion was very fast that is, t1/2<5 min. It was also observed that the metal ion-sorption capacities of the resin were pH-dependent and its selectivity toward the metal ions used is in the following order: Cu2+>Fe3+ >Cr3+>Ni2+>Co2+>Zn2+ >Cd2+>As3+>Pb2+. John Wiley & Sons 2001 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/114592/1/114592.pdf Lutfor, M. R. and Sidik, S. and Wan Yunus, W. M. Z. and Rahman, M. Z. A. and Mansor, A. and Haron, M. J. (2001) Synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch. Journal of Applied Polymer Science, 79 (7). pp. 1256-1264. ISSN 0021-8995; eISSN: 1097-4628 https://onlinelibrary.wiley.com/doi/10.1002/1097-4628(20010214)79:7%3C1256::AID-APP130%3E3.0.CO;2-G 10.1002/1097-4628(20010214)79:7<1256::AID-APP130>3.0.CO;2-G
spellingShingle Lutfor, M. R.
Sidik, S.
Wan Yunus, W. M. Z.
Rahman, M. Z. A.
Mansor, A.
Haron, M. J.
Synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch
title Synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch
title_full Synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch
title_fullStr Synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch
title_full_unstemmed Synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch
title_short Synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch
title_sort synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch
url http://psasir.upm.edu.my/id/eprint/114592/
http://psasir.upm.edu.my/id/eprint/114592/
http://psasir.upm.edu.my/id/eprint/114592/
http://psasir.upm.edu.my/id/eprint/114592/1/114592.pdf