Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.784323
Title: Reactivity of biomass relevant esters and alcohols in acidic ionic liquids
Author: Ismail, Nur Liyana Binti
ISNI:       0000 0004 7969 8770
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2019
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Abstract:
Reactivity of biomass relevant alcohols and esters in hydrogen sulfate based ionic liquids were successfully studied. A series of alcohols; methanol, 1-butanol, 2-butanol, isopropanol, and phenol were reacted with 1-butylimidazolium hydrogen sulfate [HC4im][HSO4] to represent cellulose hydroxyl group reactivity in the selected acidic ionic liquids. Apart from phenol, all selected alcohols were found to undergo sulfation via nucleophilic substitution by [HSO4]− anion after 24 h. Mechanistic study of the nucleophilic substitution reactions of p-substituted benzyl alcohols with [HC4im][HSO4] and [C4C1im][HSO4] were done using Hammett equation. The concave upward Hammett plots suggest there is a change in mechanism, from SN1 for electron donating substituents (OMe and Me) to SN2 for electron withdrawing substituents (H, Cl, CF3 and NO2). This chapter revealed that ILs can act as a solvent as well as a nucleophile in one reaction. Most importantly, this showed that sulfation of cellulose is probable under Ionosolv pretreatment. Hydrolysis of lignin-carbohydrate linkage model compounds, BHB and THFF were carried out in [HC4im][HSO4] with varying acid and water content. The rates of hydrolysis were increasing with increasing of mol% acid. The mechanistic insights of the reactions were studied using Zucker-Hammett, Bunnett-Olsen and Eyring equations. All three resulted plots are in agreement with A2 mechanism. Transesterification reactions of BHB and ethyl lactate and methanol in [HC4im][HSO4] were found to give low yields due to the sulfation of methanol. This again showed that the [HSO4]¯anion are reactive and nucleophilic enough to undergo nucleophilic substitution reaction with alcohol at 80 - 120 °C in aqueous or non-aqueous condition.
Supervisor: Welton, Tom ; Hallett, Jason Sponsor: Universiti Teknologi MARA
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.784323  DOI:
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