Thermodynamics and rheology of partially miscible polymer blends

The phase behaviour of two partially miscible binary polymer blend systems was investigated using rheological, optical, turbidimetric and light-scattering techniques. Rheological techniques included the evaluation of linear and non-linear rheology using parallel plate, sliding plate and capillary...

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Main Author: Chopra, Divya
Format: Others
Language:English
Published: 2009
Online Access:http://hdl.handle.net/2429/12972
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spelling ndltd-UBC-oai-circle.library.ubc.ca-2429-129722018-01-05T17:36:34Z Thermodynamics and rheology of partially miscible polymer blends Chopra, Divya The phase behaviour of two partially miscible binary polymer blend systems was investigated using rheological, optical, turbidimetric and light-scattering techniques. Rheological techniques included the evaluation of linear and non-linear rheology using parallel plate, sliding plate and capillary rheometry. The two systems comprised a) a model upper critical solution temperature mixture of varying M[sub w] (4.3-162 kg/mol) poly(dimethylsiloxane) and high molecular weight (M[sub w] = 83.8 kg/mol) poly(ethylmethylsiloxane) [PDMS/PEMS]; and b) a lower critical solution temperature mixture of high M[sub w] (100-200 kg/mol) poly(styrene-co-maleic anhydride) and poly(methyl methacrylate) [SMA/PMMA] with SMA component having 8%, 14% and 32% by weight maleic anhydride content (MA). The Theologically determined phase separation temperature was marked by changes in the temperature dependence of the elastic moduli at constant frequency and of the stresses at constant shear rate. Failure of time-temperature superposition in frequency sweeps in the linear region was also observed. The phase diagrams of the blends were modeled by using a temperature dependent expression for the interaction parameter of Flory-Huggins theory, based on the concept of generalized Gibbs free energy of mixing. The phase behaviour, morphology and interfacial tension of PDMS/PEMS blends was very sensitive to the molecular weight of the individual components. Miscibility increased and interfacial tension decreased as the molecular weight of PDMS decreased. SMA/PMMA blends containing 14% MA were found to be more miscible than those containing 8% or 32% MA, a finding attributed to the compositional dependence of intermolecular (SMA-SMA) and intramolecular (SMA-PMMA) interactions in the different samples. Shear-induced fibrillar type growth of SMA inclusions in the phase-separated region in the case of SMA/PMMA with 32%MA was established using rheological tools. Applied Science, Faculty of Chemical and Biological Engineering, Department of Graduate 2009-09-22T02:08:16Z 2009-09-22T02:08:16Z 2002 2002-05 Text Thesis/Dissertation http://hdl.handle.net/2429/12972 eng For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use. 6938595 bytes application/pdf
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language English
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description The phase behaviour of two partially miscible binary polymer blend systems was investigated using rheological, optical, turbidimetric and light-scattering techniques. Rheological techniques included the evaluation of linear and non-linear rheology using parallel plate, sliding plate and capillary rheometry. The two systems comprised a) a model upper critical solution temperature mixture of varying M[sub w] (4.3-162 kg/mol) poly(dimethylsiloxane) and high molecular weight (M[sub w] = 83.8 kg/mol) poly(ethylmethylsiloxane) [PDMS/PEMS]; and b) a lower critical solution temperature mixture of high M[sub w] (100-200 kg/mol) poly(styrene-co-maleic anhydride) and poly(methyl methacrylate) [SMA/PMMA] with SMA component having 8%, 14% and 32% by weight maleic anhydride content (MA). The Theologically determined phase separation temperature was marked by changes in the temperature dependence of the elastic moduli at constant frequency and of the stresses at constant shear rate. Failure of time-temperature superposition in frequency sweeps in the linear region was also observed. The phase diagrams of the blends were modeled by using a temperature dependent expression for the interaction parameter of Flory-Huggins theory, based on the concept of generalized Gibbs free energy of mixing. The phase behaviour, morphology and interfacial tension of PDMS/PEMS blends was very sensitive to the molecular weight of the individual components. Miscibility increased and interfacial tension decreased as the molecular weight of PDMS decreased. SMA/PMMA blends containing 14% MA were found to be more miscible than those containing 8% or 32% MA, a finding attributed to the compositional dependence of intermolecular (SMA-SMA) and intramolecular (SMA-PMMA) interactions in the different samples. Shear-induced fibrillar type growth of SMA inclusions in the phase-separated region in the case of SMA/PMMA with 32%MA was established using rheological tools. === Applied Science, Faculty of === Chemical and Biological Engineering, Department of === Graduate
author Chopra, Divya
spellingShingle Chopra, Divya
Thermodynamics and rheology of partially miscible polymer blends
author_facet Chopra, Divya
author_sort Chopra, Divya
title Thermodynamics and rheology of partially miscible polymer blends
title_short Thermodynamics and rheology of partially miscible polymer blends
title_full Thermodynamics and rheology of partially miscible polymer blends
title_fullStr Thermodynamics and rheology of partially miscible polymer blends
title_full_unstemmed Thermodynamics and rheology of partially miscible polymer blends
title_sort thermodynamics and rheology of partially miscible polymer blends
publishDate 2009
url http://hdl.handle.net/2429/12972
work_keys_str_mv AT chopradivya thermodynamicsandrheologyofpartiallymisciblepolymerblends
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