Journal
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS
Volume 39, Issue 15, Pages 1766-1777Publisher
JOHN WILEY & SONS INC
DOI: 10.1002/polb.1150
Keywords
dendrimer; globular transition; thermodynamic properties; heat capacity; thermal expansion; compressibility
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The pressure-volume-temperature and thermal properties of dendrimers based on benzyl ether were measured and compared with literature values for monodisperse, linear polystyrenes. In addition, property measurements are presented for an exact linear analogue to the fifth-generation dendrimer. The thermodynamic properties' molecular weight behavior for the dendrimers is unique when compared with that of linear polystyrene. All of the evidence presented in this work suggests that some form of structural transition occurs in the bulk at a molecular mass near that for the fourth-generation dendrimer. No such transition is seen for polystyrene. Dendrimers exhibit an increased packing efficiency as evidenced by a decreased specific volume (increased density) as compared with an exact linear analogue of the fifth-generation dendrimer analogue, and the dendrimer highlights the entropic differences between the two molecules. In addition, differences in the change in heat capacity with temperature for the two systems further allude to their entropic differences. A crystalline state can be formed for the lower generation dendrimer and linear analogue. This crystalline state is not seen in dendrimers above the third generation. These behaviors compiled with the difference in the glass-transition temperature for the linear analogue suggest that the dendrimers' microstructure has a significant influence on the bulk thermodynamic state of the material. The Tait equation was fitted to the volume data for comparative purposes; the Tait equation has known limitations but was selected because of its widespread application. (C) 2001 John Wiley & Sons, Inc.
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