The pyrolysis kinetics of the conversion of Malaysian kaolin to metakaolin

The aim of this work was to study the pyrolysis kinetics of the thermal transformation of kaolin to metakaolin with the aid of models and model free isoconversional methods. Thermal treatment in the range of 600–850 °C is used to convert kaolin into an amorphous and highly reactive metakaolin (MK)....

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Main Authors: Irfan Khan, M., Khan, H.U., Azizli, K., Sufian, S., Man, Z., Siyal, A.A., Muhammad, N., Faiz ur Rehman, M.
Format: Article
Published: Elsevier Ltd 2017
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85020305012&doi=10.1016%2fj.clay.2017.05.017&partnerID=40&md5=d2069ef057004f08f0f4cc44ea2872f4
http://eprints.utp.edu.my/19360/
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spelling my.utp.eprints.193602018-04-20T00:22:01Z The pyrolysis kinetics of the conversion of Malaysian kaolin to metakaolin Irfan Khan, M. Khan, H.U. Azizli, K. Sufian, S. Man, Z. Siyal, A.A. Muhammad, N. Faiz ur Rehman, M. The aim of this work was to study the pyrolysis kinetics of the thermal transformation of kaolin to metakaolin with the aid of models and model free isoconversional methods. Thermal treatment in the range of 600–850 °C is used to convert kaolin into an amorphous and highly reactive metakaolin (MK). In this study, the thermal transformation of kaolin to metakaolin was investigated using thermokinetics and instrumental analysis. Kaolin was subjected to thermogravimetric analysis (TGA) at heating rates of 10, 20 and 40 °C/min, in the temperature range of 50–800 °C. Approximately, 14.2 of mass loss was recorded during the TG analysis. 95 of the degree of dehydroxylation was attained at 635 °C, representing the minimum temperature for this process. The TGA and its related data were analyzed using model free (based on DTG, DTA and TG) and model based kinetics methods. Both DTG and DTA peak temperatures were employed for the thermokinetics of kaolin using Ozawa, Kissinger and Starink methods; giving an Ea in the range of 246.6–252.5 kJ·mol− 1. A slight higher average Ea (266–267 kJ·mol− 1 vs 246.6–252.5 kJ·mol− 1) was observed when TGA based integral methods (KAS, FWO and Starink) were used. The mechanism of the thermokinetics was investigated using the Redfern model and the best fitting was given by 3rd order chemical reaction (F3) function. Both model-free and model based thermokinetics methods could be used to validate the thermal transformation of kaolinite to metakaolinite. © 2017 Elsevier B.V. Elsevier Ltd 2017 Article PeerReviewed https://www.scopus.com/inward/record.uri?eid=2-s2.0-85020305012&doi=10.1016%2fj.clay.2017.05.017&partnerID=40&md5=d2069ef057004f08f0f4cc44ea2872f4 Irfan Khan, M. and Khan, H.U. and Azizli, K. and Sufian, S. and Man, Z. and Siyal, A.A. and Muhammad, N. and Faiz ur Rehman, M. (2017) The pyrolysis kinetics of the conversion of Malaysian kaolin to metakaolin. Applied Clay Science, 146 . pp. 152-161. http://eprints.utp.edu.my/19360/
institution Universiti Teknologi Petronas
building UTP Resource Centre
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Petronas
content_source UTP Institutional Repository
url_provider http://eprints.utp.edu.my/
description The aim of this work was to study the pyrolysis kinetics of the thermal transformation of kaolin to metakaolin with the aid of models and model free isoconversional methods. Thermal treatment in the range of 600–850 °C is used to convert kaolin into an amorphous and highly reactive metakaolin (MK). In this study, the thermal transformation of kaolin to metakaolin was investigated using thermokinetics and instrumental analysis. Kaolin was subjected to thermogravimetric analysis (TGA) at heating rates of 10, 20 and 40 °C/min, in the temperature range of 50–800 °C. Approximately, 14.2 of mass loss was recorded during the TG analysis. 95 of the degree of dehydroxylation was attained at 635 °C, representing the minimum temperature for this process. The TGA and its related data were analyzed using model free (based on DTG, DTA and TG) and model based kinetics methods. Both DTG and DTA peak temperatures were employed for the thermokinetics of kaolin using Ozawa, Kissinger and Starink methods; giving an Ea in the range of 246.6–252.5 kJ·mol− 1. A slight higher average Ea (266–267 kJ·mol− 1 vs 246.6–252.5 kJ·mol− 1) was observed when TGA based integral methods (KAS, FWO and Starink) were used. The mechanism of the thermokinetics was investigated using the Redfern model and the best fitting was given by 3rd order chemical reaction (F3) function. Both model-free and model based thermokinetics methods could be used to validate the thermal transformation of kaolinite to metakaolinite. © 2017 Elsevier B.V.
format Article
author Irfan Khan, M.
Khan, H.U.
Azizli, K.
Sufian, S.
Man, Z.
Siyal, A.A.
Muhammad, N.
Faiz ur Rehman, M.
spellingShingle Irfan Khan, M.
Khan, H.U.
Azizli, K.
Sufian, S.
Man, Z.
Siyal, A.A.
Muhammad, N.
Faiz ur Rehman, M.
The pyrolysis kinetics of the conversion of Malaysian kaolin to metakaolin
author_facet Irfan Khan, M.
Khan, H.U.
Azizli, K.
Sufian, S.
Man, Z.
Siyal, A.A.
Muhammad, N.
Faiz ur Rehman, M.
author_sort Irfan Khan, M.
title The pyrolysis kinetics of the conversion of Malaysian kaolin to metakaolin
title_short The pyrolysis kinetics of the conversion of Malaysian kaolin to metakaolin
title_full The pyrolysis kinetics of the conversion of Malaysian kaolin to metakaolin
title_fullStr The pyrolysis kinetics of the conversion of Malaysian kaolin to metakaolin
title_full_unstemmed The pyrolysis kinetics of the conversion of Malaysian kaolin to metakaolin
title_sort pyrolysis kinetics of the conversion of malaysian kaolin to metakaolin
publisher Elsevier Ltd
publishDate 2017
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85020305012&doi=10.1016%2fj.clay.2017.05.017&partnerID=40&md5=d2069ef057004f08f0f4cc44ea2872f4
http://eprints.utp.edu.my/19360/
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