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Data · dataset · 2026

Adding value to waste glycerol to produce renewable fuels and chemicals

Listed in ZivaHub and Deakin Research Online and DMU Figshare and UCL Research Data Repository — shown once because both records carry DOI 10.17034/32633625.v1

This thesis presents the results of research into the value addition of glycerol, as a by-product from biodiesel production.

Description

A number of different catalytic systems were developed involving two different pathways of value additions; (1) the esterification of glycerol with acetic acid to produce acetin esters, and (2) the transesterification of glycerol with dimethyl carbonate to produce glycerol carbonate. In the esterification of glycerol with acetic acid, two catalytic systems were developed.

A homogeneous system which used nitrogen based Brønsted-acidic ionic liquids and a heterogeneous system which used tin-exchanged tungstophosphoric acid supported on K-10 montmorillonite clay. In the homogeneous system a number of ionic liquids were tested in the reaction, with n-methyl-2-pyrollidinium hydrogen sulphate found to be the most active. The reaction conditions were optimised using a design of experiments approach, and the reusability of the catalyst was examined.

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In the heterogeneous system the effect of heteropolyacid loading and level of metal substitution were investigated. 20 wt% Sn1DTP/K-10 was found to be the most active catalyst, with the effect of reaction parameters and catalyst reusability examined using this catalyst. This catalyst was also used in preliminary continuous flow investigations. In the transesterification of glycerol with dimethyl carbonate to produce glycerol carbonate a series of metal oxide supported sodium aluminate catalysts were prepared.

The effect of preparation method (wet impregnation vs. mechanochemical preparation), metal oxide support and loading of sodium aluminate. Of all the catalysts prepared 20 wt% sodium aluminate on alumina was found to be the most stable catalyst. The effect of calcination temperature on this catalyst was also investigated with increasing calcination temperature resulting in decreased initial catalytic activity but increased catalyst reusability.<br><br><br>

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Provenance · 4 source records, 8 field assertions
SourceKeyLast seenRaw
ZivaHuboai:figshare.com:article/3263362512 d agoJSON v1
Deakin Research Onlineoai:figshare.com:article/3263362512 d agoJSON v1
DMU Figshareoai:figshare.com:article/3263362512 d agoJSON v1
UCL Research Data Repositoryoai:figshare.com:article/3263362512 d agoJSON v1
FieldAssertionExtractorEvidence
concepts[field].local:field:earth-environmentalmapping · rdr ucl ac ukconnector:rdr_ucl_ac_uk@1.0.0
concepts[field].local:field:earth-environmentalmapping · zivahub uct ac zaconnector:zivahub_uct_ac_za@1.0.0
concepts[field].local:field:earth-environmentalmapping · dro deakin edu auconnector:dro_deakin_edu_au@1.0.0
concepts[field].local:field:earth-environmentalmapping · figshare dmu ac ukconnector:figshare_dmu_ac_uk@1.0.0
descriptionsource · zivahub uct ac zaconnector:zivahub_uct_ac_za@1.0.0/metadata/dc/description
license_textsource · zivahub uct ac zaconnector:zivahub_uct_ac_za@1.0.0
publication_datesource · zivahub uct ac zaconnector:zivahub_uct_ac_za@1.0.0
titlesource · zivahub uct ac zaconnector:zivahub_uct_ac_za@1.0.0/metadata/dc/title