Why many polymers are so fragile
Creators
- 1. Department of Polymer Science, University of Akron, Akron, OH 44325-3909 (United States)
- 2. Institute of Automation and Electrometry, Russian Academy of Sciences, Novosibirsk, 630090 (Russian Federation)
- 3. Polymer Division, National Institute of Standards and Technology, Gaithersburg, MD 20899 (United States)
Description
Many polymers exhibit extremely high fragility and deviate from most of the trends known for non-polymeric glass-forming systems. The analysis of literature data presented here demonstrates that chain rigidity might be the main reason for this peculiar behaviour. Based on this analysis a simple scenario is proposed: (i) oligomers (short polymeric chains) follow trends characteristic for non-polymeric systems; (ii) increase in molecular weight (MW) does not affect structural relaxation significantly in the case of flexible chains; (iii) however, it slows down structural relaxation in rigid chains tremendously. As a result, a strong increase of Tg with MW is observed for rigid polymers. This rise in Tg leads to extremely high 'apparent' fragility and failure of usual correlations between the fragility and other parameters in rigid polymers
Additional details
Identifiers
- DOI
- 10.1088/0953-8984/19/20/205116;
- PII
- S0953-8984(07)35479-9;
Publishing Information
- Journal Title
- Journal of Physics. Condensed Matter
- Journal Volume
- 19
- Journal Issue
- 20
- Journal Page Range
- p. 205116
- ISSN
- 0953-8984
- CODEN
- JCOMEL
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 38077842
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- CORRELATIONS; FAILURES; GLASS; MOLECULAR WEIGHT; PHASE STABILITY; PHASE STUDIES; POLYMERS; RELAXATION
- Descriptors DEC
- STABILITY