Dynamic mechanical spectroscopy of plastic crystalline states in n-alkane systems

Citation
Mj. Nowak et Sj. Severtson, Dynamic mechanical spectroscopy of plastic crystalline states in n-alkane systems, J MATER SCI, 36(17), 2001, pp. 4159-4166
Citations number
18
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
JOURNAL OF MATERIALS SCIENCE
ISSN journal
00222461 → ACNP
Volume
36
Issue
17
Year of publication
2001
Pages
4159 - 4166
Database
ISI
SICI code
0022-2461(200109)36:17<4159:DMSOPC>2.0.ZU;2-D
Abstract
Dynamic mechanical spectroscopy (DMS) and differential scanning calorimetry (DSC) were used to study the plastic crystalline region of several model n -alkane systems and a commercial paraffin wax. Results indicate that DMS pr ovides a valuable complement to existing tools for locating plastic crystal line or rotator states and characterizing the pre-melting region containing these mesophases. DMS measurements demonstrate that the mechanical propert ies of plastic crystalline states in n-alkanes are difficult to isolate, an d that observed viscoelasticity surrounding the mesophases is in great part due to transitions between phases, not the rotator phases themselves. This is indicated from DMS curves that show the dynamic moduli of rotator phase s are inhibited from achieving equilibrium values due to the close proximit y of successive transitions. Furthermore, study of a system in which stabil ity of a single rotator phase has been extended through strategic blending of n-alkanes shows that dynamic mechanical properties return to near pre-me sophase values when sufficient opportunity following a transition is provid ed. These results demonstrate that many n-alkane blends can possess a short temperature interval over which the material oscillates between Hookean an d viscous behavior, controlling their performance and possibly providing fo r new applications requiring changes in viscoelastic properties in a narrow temperature span. (C) 2001 Kluwer Academic Publishers.