Synthesis of novel polymers of intrinsic microporosity for gas and vapour adsorption
dc.contributor.advisor
McKeown, Neil
dc.contributor.advisor
Ferrari, Maria-Chiara
dc.contributor.advisor
Lloyd-Jones, Guy
dc.contributor.author
Xu, Wan Ting
dc.contributor.author
Xu, Emily
dc.contributor.sponsor
DTRA
en
dc.date.accessioned
2024-09-13T12:23:49Z
dc.date.available
2024-09-13T12:23:49Z
dc.date.issued
2024-09-13
dc.description.abstract
Polymers of intrinsic microporosity (PIMs) are a class of highly porous polymeric materials, within
which the microporosity originates from the inability of the rigid and contorted polymeric chains to
pack efficiently. PIMs exhibit outstanding solution processability, large surface areas and great
structural tunability, which makes them promising materials for a range of applications, such as gas
separation, catalysis and sensors. Furthermore, their highly porous nature, along with gas separation
performances, makes PIMs excellent materials for gas adsorption applications, which includes the
capturing and storage of CO2, and the deactivation of chemical warfare agents (CWAs), as they can
efficiently store a significant volume of adsorbate in their pores, which are flexible due to the lack of a
covalent network structure. Additionally, their macromolecular structures can be tailored to show
special selectivity towards the target gases.
The project described in this thesis explored ways to further enhance the gas adsorption
properties of PIMs, via three approaches. First, the incorporation of additional basic, and nucleophilic
functionality onto PIMs was investigated to induce additional acid-base interactions with acidic gases
such as CO2, and the potential catalytic reactivity towards electrophilic compounds such as
organophosphorus-based CWAs. A PIM containing pyridine units was synthesised, and further
functionalised with amidoxime groups. The effect of the basic and nucleophilic functional groups
incorporation on PIMs were studied by comparing their polymer properties, and performances in areas
such as CO2 adsorption, CWA deactivation, and gas separation of the synthesised polymers against that
of related PIM-1 and AO-PIM-1. Secondly, the synthesis of the extremely bulky and rigid structural unit,
naphthopleiadene (NP), with in-built amine functionalities was explored to enhance the porosity of
PIMs, and to increase the affinity of polar gases such as CO2 towards PIMs. Finally, the synthesis of
some -CF3 containing monomers were attempted. These fluorinated PIMs were expected to minimise
interactions between polymeric chains, thus offering the possibility of altered solubility, and reducing
the impact of weak interchain interactions on the porosity, and further enhance the hydrophobicity of
PIMs to increase their selectivity of the target gas molecules over water vapours.
en
dc.identifier.uri
https://hdl.handle.net/1842/42156
dc.identifier.uri
http://dx.doi.org/10.7488/era/4877
dc.language.iso
en
en
dc.publisher
The University of Edinburgh
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dc.subject
adsorption
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dc.subject
microporous organic polymers
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dc.subject
PIMs
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dc.subject
carbon dioxide capture
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dc.subject
nucleophilic functionality
en
dc.subject
naphthopleiadene
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dc.subject
fluorinated PIMs
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dc.title
Synthesis of novel polymers of intrinsic microporosity for gas and vapour adsorption
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dc.type
Thesis or Dissertation
en
dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
en
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