Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.690319
Title: Expanding beyond the micropore : harnessing pendant silanols within hierarchically porous aluminophosphates for targeted catalysis
Author: Newland, Stephanie
ISNI:       0000 0004 5922 8683
Awarding Body: University of Southampton
Current Institution: University of Southampton
Date of Award: 2016
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Thesis embargoed until 23 Jun 2019
Access from Institution:
Abstract:
Discrete solid-acid centres within hierarchically porous (HP) architectures, which contain micropores with interconnected mesopores, offer the potential to overcome the diffusional limitations in the conventional microporous zeotypes. This thesis presents a design strategy to synthesise hierarchically porous isomorphously metal (Me) substituted aluminophosphates (AlPOs) and silicoaluminophosphates (SAPOs), with AFI and CHA frameworks, as a means to create a solid acid catalyst for both the liquid and vapour phase Beckmann rearrangement with enhanced catalyst lifetimes, catalyst activity and substrate versatility. By employing a one-step soft templating approach coupled with detailed physicochemical and spectroscopic characterisation, isolated solid acid sites can be suitably tailored and discretely modulated within the micropores and mesopores. The resulting HP SAPOs and AlPOs were designed to possess an auxiliary mesoporous network (as confirmed via pXRD, BET and N2 isotherms), to mimic the microporous analogues active sites and to have additional active silanol sites lining the mesopores (as confirmed via FTIR spectroscopy, NMR spectroscopy and TPD). Owing to the interplay between mesoporosity, Brønsted acidity and silanol sites the HP catalysts were shown to have superior catalytic properties to the microporous analogues. The HP AlPO’s potential as scaffolds for the heterogenisation of bulky functional groups was also assessed. The pendant silanols were harnessed to covalent anchor an imidazolium organocatalyst to the HP mesopores. The resulting catalyst was active in the formation of cyclic carbenes from epoxide and CO2. Thus, this further highlighted the efficacy of our design rationale in the synthesis of HP AlPOs and its amenability for creating a range of active sites for catalysis.
Supervisor: Raja, Robert Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.690319  DOI: Not available
Share: