Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368094
Title: Studies of clay-polymer interactions
Author: Hatharasinghe, Henegama Liyanage Mallika
ISNI:       0000 0001 3546 1171
Awarding Body: University of London
Current Institution: University College London (University of London)
Date of Award: 2001
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Abstract:
The clay-polymer interactions have been investigated by experiments on a four-component system consisting of n-butylammonium vermiculite clay, n-butylammonium chloride, polyethylene oxide (PEO) and water. The inter-platelet distance, d was studied by neutron diffraction as a function of the clay volume fraction r, the salt concentration c and the molecular weight Mw and volume fraction of the PEO v in the system. The most conspicuous results is that PEO addition only brings about a contraction in the d spacing when the mean end-to-end distance l of PEO is greater than or equal to daq (d spacing in the clay-salt-water system). The structure of the gel phase was studied using H/D isotope substitution of polymer. The results indicate that a significant part of the polymer chains are directly bound to the clay surfaces. With r, c, v constant, d is independent of Mw, ruling out the depletion mechanism. The results fitted well to a model of bridging flocculation. The strength of the bridging force was determined by mapping d vs. v data onto previously determined d vs. p (uniaxial stress) data obtained for the same clay-salt-water system without added polymer. The drawing force depends on knowing v inside the gel, which was determined to be 45% of added PEO by refractometry and chemical analyses. Using this value gave a drawing force per bridge of 0.6pN and this finding represents a new challenge in colloid and polymer science. Previous studies of the three-component system showed that a phase transition from gel to tactoid occurred as the temperature increases. In our studies a gel to tactoid transition was found to occur when the temperature was decreased through the freezing point of solution. These both upper and lower phase transitions have been studied as a function of Mw, v and c by diffraction techniques and interestingly they were found to be completely reversible and sharp even with added polymer. Neither the transition temperature nor the d spacing of the clay tactoid phase was affected by the addition of PEO.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.368094  DOI: Not available
Keywords: Physical chemistry
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