Physical Properties of PBMA‐b‐PBA‐b‐PBMA Triblock Copolymers Synthesized by Atom Transfer Radical Polymerization
Abstract
Abstract The physical properties of well‐defined poly(butyl methacrylate)‐block‐poly(butyl acrylate)‐block‐poly(butyl methacrylate) (PBMA‐b‐PBA‐b‐PBMA) triblock copolymers synthesized by atom transfer radical polymerization (ATRP) are reported. The glass transition and the degradation temperature of copolymers were determined by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). DSC measurements showed phase separation for all of the copolymers with the exception of the one with the shortest length of either inner or outer blocks. TGA demonstrated that the thermal stability of triblock copolymers increased with decreasing BMA content. Dynamic mechanical analysis was used for a preceding evaluation of adhesive properties. In these block copolymers, the deformation process under tension can take place either homogeneously or by a neck formation depending on the molecular weight of the outer BMA blocks and on the length of the inner soft BA segments. Microindentation measurements were also performed for determining the superficial mechanical response and its correlation with the bulk behavior. Stress‐strain curves for the different PBMA‐b‐PBA‐b‐PBMA specimens at room temperature and at 10 mm/min. magnified image Stress‐strain curves for the different PBMA‐b‐PBA‐b‐PBMA specimens at room temperature and at 10 mm/min.
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The all acrylic-based high temperature TPEs containing poly(1-adamatyl acrylate) as hard domain and poly(tetrahydrofurfuryl acrylate) as soft domain exhibited superior stress-strain behavior compared to conventional all acrylic-based TPEs consisting of PMMA and PBA made by controlled radical processes.
“These TPEs exhibited superior stress-strain behavior compared to that of conventional all acrylic-based TPEs consisting of PMMA and PBA made by controlled radical processes [94], while the tensile strength was lower compared to that of similar products prepared via living anionic polymerization [95].”
From Block Copolymers: Synthesis, Self-Assembly, and Applications (2017) · cites this paper as [94]
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Block Copolymers: Synthesis, Self-Assembly, and Applications
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“…TPEs exhibited superior stress-strain behavior compared to that of conventional all acrylic-based TPEs consisting of PMMA and PBA made by controlled radical processes [94], while the tensile strength was lower compared to that of similar products prepared via living anionic polymerization [95].”
Background
- Authors
- Martín‐Gomis, L., Fernández‐García, M., de la Fuente, J. L., Madruga, E. L., & Cerrada, M. L.
- Affiliations
- Consejo Superior de Investigaciones Científicas (ES)
- Corresponding author
- Fernández‐García, Marta
- Venue
- Macromolecular Chemistry and Physics
- Publisher
- Wiley
- Published
- 2003-10-28
- Volume
- 204
- Issue
- 16
- Pages
- 2007-2016
- ISSN
- 1022-1352 (ISSN-L)
- 1521-3935
- OpenAlex
- W1969362700
- Cited by
- 12
- References
- 47
- Citations by year
- 2024: 1 · 2017: 1 · 2016: 1 · 2014: 2 · 2013: 1 · 2012: 1
- FWCI
- 0.47
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Macromolecular Chemistry and Physics (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Physical Sciences › Materials Science › Materials Chemistry › Block Copolymer Self-Assembly
- Physical Sciences › Materials Science › Polymers and Plastics › Polymer crystallization and properties
- Keywords
- triblock copolymers, poly(butyl methacrylate), poly(butyl acrylate), atom transfer radical polymerization, glass transition, thermal stability, adhesive properties, neck formation, microindentation, stress-strain behavior
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