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Journal ArticleDOI

Thermoplastic elastomers by hydrogen bonding 1. Rheological properties of modified polybutadiene

R. Stadler, +1 more
- 01 Sep 1986 - 
- Vol. 264, Iss: 9, pp 773-778
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TLDR
In this paper, a polybutadiene of narrow molecular weight distribution was modified using 4-phenyl-1, 2,4-triazoline-3,5-dione.
Abstract
Polybutadiene of narrow molecular weight distribution was modified using 4-phenyl-1, 2,4-triazoline-3,5-dione. The degree of modification was 1% and 2% with respect to the repeating units. Hydrogen bonding between the highly polar urazole groups thus incorporated into the polymer gives rise to the formation of a thermoreversible elastomeric network. Dynamic mechanical measurements in the temperature range between 220 and 330 K support the picture of the thermoreversible hydrogen bond interaction. The rubber elastic plateau is shifted to higher temperatures and lower frequencies. The increase in the plateau modulus cannot be attributed solely to the contribution of the network structure but is mainly a consequence of the broadening of the relaxation time spectrum in the modified samples. From the temperature dependence of the shift factors log(aT) it is concluded that the general WLF approach fails. The strong temperature dependence of the apparent activation energy of flow is a consequence of the temperature dependence of the hydrogen bond interaction.

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Self-healing and thermoreversible rubber from supramolecular assembly

TL;DR: The design and synthesis of molecules that associate together to form both chains and cross-links via hydrogen bonds and the system shows recoverable extensibility up to several hundred per cent and little creep under load are designed and synthesized.
Journal ArticleDOI

Self‐Healing Polymers via Supramolecular Forces

TL;DR: This Review describes recent examples and concepts of supramolecular polymers based on hydrogen bonding, π-π interactions, ionomers, and coordinative bonds, thus convincingly discussing the advantages and versatility of these supramolescular forces for the design and realization of self-healing polymers.
Journal ArticleDOI

Physical chemistry of supramolecular polymer networks

TL;DR: This critical review summarizes the current state of the art in the physical-chemical characterization of supramolecular networks and relates this knowledge to that about classical, covalently jointed and crosslinked networks.
Journal ArticleDOI

Model Transient Networks from Strongly Hydrogen-Bonded Polymers

TL;DR: In this article, random copolymers consisting of n-butyl acrylate backbones with quadruple hydrogen-bonding side chains based on 2-ureido-4[1H]-pyrimidinone (UPy) have been synthesized via controlled radical polymerization and postpolymerization functionalization.
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Supramolecular polymers from linear telechelic siloxanes with quadruple- hydrogen- bonded units

TL;DR: In this paper, two ureidopyrimidone (UPy) functional groups are associated via quadruple hydrogen bonds in a donor-donor-acceptor−acceptor −acceptor (DDAA) array.
References
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Book

Viscoelastic properties of polymers

John D. Ferry
TL;DR: In this article, the authors describe the nature of Viscoelastic behavior of polymeric systems and approximate relations among the linear Viscoels and approximate interrelations among the Viscelastic Functions.
Journal ArticleDOI

Polymer Compatibilization Through Hydrogen Bonding

TL;DR: Partially modified polystyrene containing vinyl phenyl hexafluorodimethyl carbinol was mixed with a number of counterpolymers, including poly(vinyl-acetate), poly(methyl methacry1 ate), poly (ethy] methacelate, poly (n-butyl methace late), polyviny] methyl ether, poly(2,6 dimethyl-1,4 phenylene oxide), bisphenol A polycarbonate poly(styrene-co-acryloni-trile), poly poly(dimethyl
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Orientation and relaxation in uniaxially stretched poly(vinyl methyl ether)-atactic polystyrene blends

J.P. Faivre, +2 more
- 01 Jun 1985 - 
TL;DR: The influence of strain rate and temperature of stretching on orientation of both polymer chains in blends containing up to 25% PVME has been studied in this article, and the relaxation master curves at a reference temperature T = T g +40°C have also been determined.
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