Published May 23, 2007 | Version v1
Journal article

Why many polymers are so fragile

  • 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