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Deformation kinetics analysis of polymeric matrices
1Faculty of Pharmacy, University of Toronto, Ontario, Canada.
Pharmaceutical Research
|May 1, 1996
Summary
Understanding tablet compression kinetics, this study quantifies deformation parameters like activation volume (Vact) and activation energy (Eact) in poly(methyl methacrylate-co-methacrylic acid) (PMMA/coMAA) for improved production control.
Area of Science:
- Materials Science
- Chemical Engineering
- Pharmaceutical Technology
Background:
- Tablet compression is crucial in pharmaceutical manufacturing.
- Understanding polymer deformation kinetics is key to controlling tablet properties.
- Poly(methyl methacrylate-co-methacrylic acid) (PMMA/coMAA) serves as a model viscoelastic polymer.
Purpose of the Study:
- To quantify deformation kinetic parameters: activation volume (Vact) and activation energy (Eact).
- To investigate the predominant barrier to deformation in PMMA/coMAA.
- To provide data for a time-dependent particle deformation model.
Main Methods:
- Performed stress relaxation studies at varying temperatures using an instrumented Instron testing apparatus.
- Quantified shear stress rates via solid density, microindentation hardness, and contact area testing.
- Applied different strain rates (1, 2, and 5 mm/min) during experiments.
Main Results:
- Activation volume (Vact) values ranged from 63.8 to 79.1 b(3) across tested strain rates.
- Activation energy (Eact) for flow increased with strain rate, from 145 kJ/mole(-1) to 506 kJ/mole(-1).
- Results indicate strain hardening effects influencing polymer deformation.
Conclusions:
- The determined activation volumes and energies are essential for modeling tablet compaction.
- These parameters provide insights into the viscoelastic behavior of PMMA/coMAA during compression.
- The findings contribute to better control over tablet production parameters.