Physico-thermal properties of spinifex resin bio-polymer

Mondal, Subrata, Memmott, Paul, Wallis, Lynley and Martin, Darren (2012) Physico-thermal properties of spinifex resin bio-polymer. Materials Chemistry and Physics, 133 2-3: 692-699. doi:10.1016/j.matchemphys.2012.01.058

Author Mondal, Subrata
Memmott, Paul
Wallis, Lynley
Martin, Darren
Title Physico-thermal properties of spinifex resin bio-polymer
Journal name Materials Chemistry and Physics   Check publisher's open access policy
ISSN 0254-0584
Publication date 2012-04-16
Sub-type Article (original research)
DOI 10.1016/j.matchemphys.2012.01.058
Volume 133
Issue 2-3
Start page 692
End page 699
Total pages 8
Place of publication Lausanne, Switzerland
Publisher Elsevier
Collection year 2013
Language eng
Formatted abstract
The traditional preparation of spinifex resin for use as an adhesive by Indigenous Australians involves the application of limited heat as a source of energy for processing though overheating may cause permanent degradation of the material. This paper investigates the physico-thermal properties of spinifex resin and its traditional manufactured composite materials to manipulate morphologies and properties during handling and performance. The pure resin was found to display a low glass transition temperature (Tg), and the Tg was found to increase when it was heat-treated due to the thermally induced reaction of resin functional groups. The glass transition temperature further increased when soil minerals were incorporated within the resin matrix according to the conventional theory of hindrance of molecular motion of the polymer chains. The pure resin (metabolic compounds) contained some inorganic elements (Al, Fe, Mg, Mn, Ca, etc.) because of the micro-nutrients taken up by spinifex plants during their life span. Thermo-gravimetric analysis (TGA) revealed that the pure resin displayed the lowest thermal stability. However, the thermal stability improved for resin samples that had been extracted by solvent and subsequently heat treated. This enhanced thermal stability was most likely due to the thermally induced reaction of resin functional groups to form a crosslinked network structure.
Keyword Composite materials
Heat treatment
Glass transitions
Differential Scanning Calorimetry (DSC)
Q-Index Code C1
Q-Index Status Confirmed Code
Institutional Status UQ

Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 7 times in Thomson Reuters Web of Science Article | Citations
Scopus Citation Count Cited 9 times in Scopus Article | Citations
Google Scholar Search Google Scholar
Created: Mon, 23 Apr 2012, 10:30:50 EST by Miss Susan Theiss on behalf of School of Biological Sciences