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  • TITLE
  • CERTIFICATE-1
  • CERTIFICATE-2
  • DECLARATION
  • ACKNOWLEDGEMENT
  • Preface
  • List of Abbreviations
  • CONTENTS
  • 1. INTRODUCTION
  • 1.1 Polymer blends
  • 1.2 Classification and preparation of polymer blends
  • 1.2.1 Thermoplastic elastomers (TPEs)
  • 1.2.2 Classification of thermoplastic elastomers
  • 1 3 Thermodynamics of Miscibility
  • 1.3.1 One phase polymer blends
  • 1.4 Compatibility Predictions
  • 1.4.1 Solubility parameter approach
  • 1.5 Compatibilisation Strategy
  • 1. 5.1 Physical compatibilisation
  • (a) Compatibilisation by block copolymers
  • (b) Compatibilisation by graft copolymer
  • (c) Compatibilisation by random copolymers
  • 1.5.2 Reactive compatibilisation
  • 1.6 Mechanism for phase morphology refinement
  • 1.7 Effect of compatibilisation or interfacial thickness
  • 1.8 Interfacial stability of the copolymer
  • 1.9 Factors Affecting the Efficiency of Compatibiliser
  • 1.9.1 Chemical nature of the compatibiliser
  • 1.9.2 Copolymer chain microstructure
  • 1 9.3 Molecular mass and composition of the Copolymer
  • 1 9.4 Concentration of the copolymer
  • 1.9.5 Mode of incorporation of the compatibiliser
  • 1.10 Organisation of the Copolymer at the Blend Interface
  • 1.11 Physical Versus Reactive Blending
  • 1.12 Theories of compatibilisation
  • 1.13 Other routes of compatibilisation
  • 1.13. 1 Solution casting method
  • 1. 13.2 Dynamic cross linking
  • 1.14 Phase morphology development in physical blending
  • 1.15 Effect of physical blending on phase morphology
  • 1.16 Blends based on PS and PB
  • 1.17 Scope and objective of the work
  • 1.18 References
  • 2. EXPERIMENTAL TECHNIQUES
  • 2.1 Materials
  • 2.1.1 Polystyrene (PS)
  • 2.1.2 Polybutadiene (PB)
  • 2.1.3 Styrene butadiene rubber (SBR)
  • 2.1.4 Poly (styrene-b-butadiene-b-styrene) rubber (SBS)
  • 2.2 Preparation of the blends
  • 2.3 Measurements
  • 2.3.1 Phase morphology analysis
  • 2.3.2 Analysis of morphological parameters
  • 2.3.3 Co-continuity calculation / solvent dissolution
  • 2.3.4 Static mechanical properties
  • 2.3.5 Rheological measurements
  • 2.3.5 (1) Extrudate morphology analysis
  • (2) Melt elasticity
  • 2.3.6 Thermal properties
  • (1) Thermogravimetric analysis (TGA)
  • (2) Differential scanning calorimetric measurements (DSC)
  • 2.3.7 Dynamic mechanical analysis (DMA)
  • 2.3.8 Solid-state nuclear magnetic resonance spectroscopy (NMR) studies
  • 2.4 References
  • 3. PHASE MORPHOLOGY
  • 3.1 Introduction
  • 3.2 Results and discussion
  • 3.2.1 Influence of mixing time
  • 3.2.2 Influence of mixing temperature
  • 3.2.3 Influence of rotor speed
  • 3.2.4 Effect of blend ratio
  • 3.2.5 Cocontinuity calculation
  • 3.2.6 Effect of copolymer addition on dispersed phase size
  • 3.2.7 Comparison with theory
  • 3.2.8 Conformation of the copolymer at the interface
  • 3.2.9 Influence of annealing
  • 3.3 Conclusions
  • 3.4 References
  • 4. MECHANICAL PROPERTIES
  • 4.1 Introduction
  • 4.2 Results and discussion
  • 4.2.1 Influence of rotor speed
  • 4.2.2 Influence of mixing temperature
  • 4.2.3 Influence of mixing time
  • 4.2.4 Effect of blend ratio
  • 4.2.5 Modelling of tensile moduli
  • 4.2.6 Tensile moduli of co-continuous regions
  • 4.2.7 Effect of compatibilisation on mechanical properties
  • 4.2.8 Effect of dynamic vulcanization
  • 4.3 Conclusions
  • 4.4. References
  • 5. RHEOLOGICAL. PROPERTIES
  • 5.1 Introduction
  • 5.2 Results and discussion
  • 5.2.1 Melt viscosity
  • 5.2.2 Comparison with theoretical predictions
  • 5.2.3 Effects of compatibilisation
  • 5.2.4 Flow behavior index and consistency index values
  • 5.2.5 Melt elasticity
  • 5 2.5.1 Extrudate swell
  • 5.2.5.2 Principal normal stress difference (T11-T22)
  • 5.2.5.3 Recoverable shear strain (SR)
  • 5.2.6 Extrudate morphology
  • 5.2.6.1 Effect of blend ratio and shear rate
  • 5.2.6.2 Effect of compatibilisation
  • 5.3. Conclusions
  • 5.4. References
  • 6. THERMAL PROPERTIES
  • 6.1 Introduction
  • 6.2 Results and discussion
  • 6.2.1 Effect of blend ratio
  • 6.2.2 Effect of compatibilisation
  • 6.2.3 Kinetics of degradation
  • 6.2.4 Differential scanning calorimetry
  • 6.3 Conclusion
  • 6.4 References
  • 7. DYNAMIC MECHANICAL PROPERTIES
  • 7.1 Introduction
  • 7.2 Results and discussion
  • 7.2.1 Uncompatibilised Blends
  • 7.2.2 Modulus-composition models
  • 7.2.3 Effect of compatibilisation
  • 7.2.4 Cole-Cole plot
  • 7.2.5 Degree of entanglement density
  • 7.3 Conclusion
  • 7.4 References
  • 8. NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY
  • 8.1 Introduction
  • 8.2 Results and discussion
  • 8.2.1 NMR spectroscopy of homopolymers
  • 8.2.2 PS / PB incompatible blends
  • 8.2.3 Effect of compatibilisation
  • 8.3 Conclusions
  • 8.4 References
  • 9. GENERAL CONCLUSIONS
  • 9.1 Conclusions
  • 9.2 Future scope of the work
  • 9.2.1 Location of the Copolymer at the Interface
  • 9.2.2 Calculation of Interfacial Thickness
  • 9.2.3 Dynamically Vulcanised Blends
  • 9.2.4 Transport Studies
  • 9.2.5 Effect of Various Fillers
  • 9.2.6 Gas Permeation Studies
  • 9.2.7 Nanoparticles
  • 9.2.8 Fabrication of Useful Products
  • APPENDIX
  • CURRICULUM VITAE
  • List of Publications