Alkali-free zn–al layered double hydroxide catalysts for triglyceride transesterification

Zn–Al layered double hydroxides (LDHs) of general formula Al3+ x(OH)2]x+(CO3Zn–Al2−)x/2·yH2O are promising solid base catalysts for the transesterification of lipids to biofuels. However, conventional synthetic routes employ alkali ydroxide/carbonate precipitants which may contaminate the final LDH...

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Published in:Catalysts
Main Author: Tajuddin N.A.; Manayil J.C.; Isaacs M.A.; Parlett C.M.A.; Lee A.F.; Wilson K.
Format: Article
Language:English
Published: MDPI 2018
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85062421592&doi=10.3390%2fcatal8120667&partnerID=40&md5=9f28c517c32c180547fb74cd88e189d1
id 2-s2.0-85062421592
spelling 2-s2.0-85062421592
Tajuddin N.A.; Manayil J.C.; Isaacs M.A.; Parlett C.M.A.; Lee A.F.; Wilson K.
Alkali-free zn–al layered double hydroxide catalysts for triglyceride transesterification
2018
Catalysts
8
12
10.3390/catal8120667
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85062421592&doi=10.3390%2fcatal8120667&partnerID=40&md5=9f28c517c32c180547fb74cd88e189d1
Zn–Al layered double hydroxides (LDHs) of general formula Al3+ x(OH)2]x+(CO3Zn–Al2−)x/2·yH2O are promising solid base catalysts for the transesterification of lipids to biofuels. However, conventional synthetic routes employ alkali ydroxide/carbonate precipitants which may contaminate the final LDH catalyst and biofuel. The use of (NH3)2CO3 and NH3OH as precipitants affords alkali-free Zn–Al-LDHs spanning a wide composition range. The hydrothermal reconstruction of calcined Zn–Al-LDHs offers superior solid basicity and catalytic activity for the transesterification of C4–C18 triglycerides with methanol,compared with cold liquid phase or vapour phase reconstruction. Hydrothermally activated Zn3.3–Al-LDH was stable towards leaching during transesterification. © 2018 by the authors. Licensee MDPI, Basel, Switzerland.
MDPI
20734344
English
Article
All Open Access; Gold Open Access; Green Open Access
author Tajuddin N.A.; Manayil J.C.; Isaacs M.A.; Parlett C.M.A.; Lee A.F.; Wilson K.
spellingShingle Tajuddin N.A.; Manayil J.C.; Isaacs M.A.; Parlett C.M.A.; Lee A.F.; Wilson K.
Alkali-free zn–al layered double hydroxide catalysts for triglyceride transesterification
author_facet Tajuddin N.A.; Manayil J.C.; Isaacs M.A.; Parlett C.M.A.; Lee A.F.; Wilson K.
author_sort Tajuddin N.A.; Manayil J.C.; Isaacs M.A.; Parlett C.M.A.; Lee A.F.; Wilson K.
title Alkali-free zn–al layered double hydroxide catalysts for triglyceride transesterification
title_short Alkali-free zn–al layered double hydroxide catalysts for triglyceride transesterification
title_full Alkali-free zn–al layered double hydroxide catalysts for triglyceride transesterification
title_fullStr Alkali-free zn–al layered double hydroxide catalysts for triglyceride transesterification
title_full_unstemmed Alkali-free zn–al layered double hydroxide catalysts for triglyceride transesterification
title_sort Alkali-free zn–al layered double hydroxide catalysts for triglyceride transesterification
publishDate 2018
container_title Catalysts
container_volume 8
container_issue 12
doi_str_mv 10.3390/catal8120667
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85062421592&doi=10.3390%2fcatal8120667&partnerID=40&md5=9f28c517c32c180547fb74cd88e189d1
description Zn–Al layered double hydroxides (LDHs) of general formula Al3+ x(OH)2]x+(CO3Zn–Al2−)x/2·yH2O are promising solid base catalysts for the transesterification of lipids to biofuels. However, conventional synthetic routes employ alkali ydroxide/carbonate precipitants which may contaminate the final LDH catalyst and biofuel. The use of (NH3)2CO3 and NH3OH as precipitants affords alkali-free Zn–Al-LDHs spanning a wide composition range. The hydrothermal reconstruction of calcined Zn–Al-LDHs offers superior solid basicity and catalytic activity for the transesterification of C4–C18 triglycerides with methanol,compared with cold liquid phase or vapour phase reconstruction. Hydrothermally activated Zn3.3–Al-LDH was stable towards leaching during transesterification. © 2018 by the authors. Licensee MDPI, Basel, Switzerland.
publisher MDPI
issn 20734344
language English
format Article
accesstype All Open Access; Gold Open Access; Green Open Access
record_format scopus
collection Scopus
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