Enhanced arsenate removal by lanthanum and nano–magnetite composite incorporated palm shell waste–based activated carbon

Palm shell waste–based activated carbon (PSAC) was magnetized via hydrothermal impregnation of nano–magnetite, and further coated by various amounts of lanthanum (La) followed by calcination. Numerous batch tests were carried out to observe arsenate removal by La–impregnated, magnetized PSAC (MPSAC–...

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Main Authors: Jais, F.M., Ibrahim, S., Yoon, Y., Jang, M.
Format: Article
Published: Elsevier 2016
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Online Access:http://eprints.um.edu.my/17429/
http://dx.doi.org/10.1016/j.seppur.2016.05.034
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spelling my.um.eprints.174292017-07-04T08:50:56Z http://eprints.um.edu.my/17429/ Enhanced arsenate removal by lanthanum and nano–magnetite composite incorporated palm shell waste–based activated carbon Jais, F.M. Ibrahim, S. Yoon, Y. Jang, M. TA Engineering (General). Civil engineering (General) Palm shell waste–based activated carbon (PSAC) was magnetized via hydrothermal impregnation of nano–magnetite, and further coated by various amounts of lanthanum (La) followed by calcination. Numerous batch tests were carried out to observe arsenate removal by La–impregnated, magnetized PSAC (MPSAC–La) in aqueous phase. Isotherm data showed that MPSAC–La(0.36) (weight ratio of La to Fe = 0.36) gave the highest adsorption capacity (227.6 mg g−1), which was approximately 16.5 and 1.6 times higher than PSAC and magnetized PSAC (MPSAC), respectively. As an indication of sorption affinity, MPSAC–La(0.36) had the highest Langmuir constant (KL), which was approximately 230 times greater than that of MPSAC. Based on the pH effect and speciation modeling, arsenate was predominantly removed by precipitation at pH < 8, while it complexed on the surface of La(OH)3 at pH > 8. Lesser La dissolution resulted, owing to a strong binding effect of nano–magnetite with La. XRD, FTIR, SEM–EDS, and N2 gas isotherms showed that the coating of nano–magnetite introduced substantial clogging in the micropores of PSAC, but increased meso– and macropores. However, lanthanum oxide/hydroxide (LO/LH) glued the spaces of nano–magnetite to eliminate most pore structures, and effectively removed arsenate as LaAsO4 at pH 6. Overall, MPSAC–La(0.36) is considered a competitive granular material due to its extremely high sorption capabilities, easy magnetic separation and high regeneration rate. Elsevier 2016 Article PeerReviewed Jais, F.M. and Ibrahim, S. and Yoon, Y. and Jang, M. (2016) Enhanced arsenate removal by lanthanum and nano–magnetite composite incorporated palm shell waste–based activated carbon. Separation and Purification Technology, 169. pp. 93-102. ISSN 1383-5866 http://dx.doi.org/10.1016/j.seppur.2016.05.034 doi:10.1016/j.seppur.2016.05.034
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic TA Engineering (General). Civil engineering (General)
spellingShingle TA Engineering (General). Civil engineering (General)
Jais, F.M.
Ibrahim, S.
Yoon, Y.
Jang, M.
Enhanced arsenate removal by lanthanum and nano–magnetite composite incorporated palm shell waste–based activated carbon
description Palm shell waste–based activated carbon (PSAC) was magnetized via hydrothermal impregnation of nano–magnetite, and further coated by various amounts of lanthanum (La) followed by calcination. Numerous batch tests were carried out to observe arsenate removal by La–impregnated, magnetized PSAC (MPSAC–La) in aqueous phase. Isotherm data showed that MPSAC–La(0.36) (weight ratio of La to Fe = 0.36) gave the highest adsorption capacity (227.6 mg g−1), which was approximately 16.5 and 1.6 times higher than PSAC and magnetized PSAC (MPSAC), respectively. As an indication of sorption affinity, MPSAC–La(0.36) had the highest Langmuir constant (KL), which was approximately 230 times greater than that of MPSAC. Based on the pH effect and speciation modeling, arsenate was predominantly removed by precipitation at pH < 8, while it complexed on the surface of La(OH)3 at pH > 8. Lesser La dissolution resulted, owing to a strong binding effect of nano–magnetite with La. XRD, FTIR, SEM–EDS, and N2 gas isotherms showed that the coating of nano–magnetite introduced substantial clogging in the micropores of PSAC, but increased meso– and macropores. However, lanthanum oxide/hydroxide (LO/LH) glued the spaces of nano–magnetite to eliminate most pore structures, and effectively removed arsenate as LaAsO4 at pH 6. Overall, MPSAC–La(0.36) is considered a competitive granular material due to its extremely high sorption capabilities, easy magnetic separation and high regeneration rate.
format Article
author Jais, F.M.
Ibrahim, S.
Yoon, Y.
Jang, M.
author_facet Jais, F.M.
Ibrahim, S.
Yoon, Y.
Jang, M.
author_sort Jais, F.M.
title Enhanced arsenate removal by lanthanum and nano–magnetite composite incorporated palm shell waste–based activated carbon
title_short Enhanced arsenate removal by lanthanum and nano–magnetite composite incorporated palm shell waste–based activated carbon
title_full Enhanced arsenate removal by lanthanum and nano–magnetite composite incorporated palm shell waste–based activated carbon
title_fullStr Enhanced arsenate removal by lanthanum and nano–magnetite composite incorporated palm shell waste–based activated carbon
title_full_unstemmed Enhanced arsenate removal by lanthanum and nano–magnetite composite incorporated palm shell waste–based activated carbon
title_sort enhanced arsenate removal by lanthanum and nano–magnetite composite incorporated palm shell waste–based activated carbon
publisher Elsevier
publishDate 2016
url http://eprints.um.edu.my/17429/
http://dx.doi.org/10.1016/j.seppur.2016.05.034
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score 13.211869