Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent

Li1-xNi1+xO2powder was synthesized by polymerised complex method using malonic acid as a chelating agent. The carboxylate precursor was calcined in the temperature range 650-800°C for 14-48 h. The TG curves of malonic acid, lithium acetate dihydrate, nickel acetate tetrahydrate and the precursor wer...

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Main Authors: Titipun Thongtem, Somchai Thongtem
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/62274
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-622742018-09-11T09:24:55Z Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent Titipun Thongtem Somchai Thongtem Materials Science Li1-xNi1+xO2powder was synthesized by polymerised complex method using malonic acid as a chelating agent. The carboxylate precursor was calcined in the temperature range 650-800°C for 14-48 h. The TG curves of malonic acid, lithium acetate dihydrate, nickel acetate tetrahydrate and the precursor were studied at 29.52-600°C. The FTIR spectra of the precursor without and with 650-800°C calcination were used to explain the vibrational bonding. At 750°C and above, only Li1-xNi1+xO2phase was detected. The maximum [I(003/I(104)] and minimum [I(006+102)/I(101)] intensity ratios of the XRD spectra were used to determine the optimum temperature and time of calcination for preparation of Li1-xNi1+xO2powder. In addition, formation mechanism of Li1-xNi1+xO2is proposed. The content of nickel, lithium, Ni3+/(Ni3++ Ni2+) and mean oxidation state of nickel at 650-800°C were determined and they show very good agreement. The SEM micrograph is also used to explain the morphology of the powder. © 2004 Elsevier Ltd and Techna Group S.r.l. All rights reserved. 2018-09-11T09:24:55Z 2018-09-11T09:24:55Z 2005-01-01 Journal 02728842 2-s2.0-10444219580 10.1016/j.ceramint.2004.05.007 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=10444219580&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62274
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Materials Science
spellingShingle Materials Science
Titipun Thongtem
Somchai Thongtem
Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent
description Li1-xNi1+xO2powder was synthesized by polymerised complex method using malonic acid as a chelating agent. The carboxylate precursor was calcined in the temperature range 650-800°C for 14-48 h. The TG curves of malonic acid, lithium acetate dihydrate, nickel acetate tetrahydrate and the precursor were studied at 29.52-600°C. The FTIR spectra of the precursor without and with 650-800°C calcination were used to explain the vibrational bonding. At 750°C and above, only Li1-xNi1+xO2phase was detected. The maximum [I(003/I(104)] and minimum [I(006+102)/I(101)] intensity ratios of the XRD spectra were used to determine the optimum temperature and time of calcination for preparation of Li1-xNi1+xO2powder. In addition, formation mechanism of Li1-xNi1+xO2is proposed. The content of nickel, lithium, Ni3+/(Ni3++ Ni2+) and mean oxidation state of nickel at 650-800°C were determined and they show very good agreement. The SEM micrograph is also used to explain the morphology of the powder. © 2004 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
format Journal
author Titipun Thongtem
Somchai Thongtem
author_facet Titipun Thongtem
Somchai Thongtem
author_sort Titipun Thongtem
title Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent
title_short Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent
title_full Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent
title_fullStr Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent
title_full_unstemmed Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent
title_sort synthesis of li1-xni1+xo2 using malonic acid as a chelating agent
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=10444219580&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/62274
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