Surface Tension in Polymer Blends of Isotactic Poly(propylene) and Atactic Polystyrene

Author(s):  
Zofia Funke ◽  
Christian Schwinger ◽  
Rameshwar Adhikari ◽  
Jörg Kressler
e-Polymers ◽  
2003 ◽  
Vol 3 (1) ◽  
Author(s):  
Mileta Boyanova ◽  
Mohammed Forhad Mina ◽  
Francisco José Baltá Calleja ◽  
Stoyko Fakirov

Abstract Microhardness (H) has been used to quantitatively characterize the quality of the interphase boundary of blends of atactic polystyrene (PS) with natural rubber (NR) and the compatibilizer styrene-butadiene-styrene (SBS) block copolymer. Qualitative conclusions are drawn for the same purpose from scanning electron microscopy (SEM) observations on surface indentation. Cast films of neat PS and the blends PS/NR, PS/SBS and PS/NR/SBS were prepared from a common solvent (toluene). While neat PS shows a constant H = 175 MPa, the PS/SBS blend exhibits a gradual decrease starting from H = 130 - 140 MPa at a distance of about 100 μm from the phase boundary up to the final value of 25 MPa. For the PS/NR blend this decrease starts at about 50 μm, reaching the same final value. Owing to the elastic recovery, no indentations on the NR or SBS particles surface can be detected as confirmed by SEM. The compatibilized blend PS/NR/SBS is characterized by the thinnest phase boundary (about 25 μm) and a final H value of 75 MPa which demonstrates that the compatibilizer SBS is distributed just on the phase boundary between PS and NR. Results confirm previous findings in incompatible blends of poly(methyl methacrylate)/NR, highlighting that microindentation is a sensitive tool for studying the breadth and quality of the interphase boundary in compatibilized or non-compatibilized polymer blends and other non-homogeneous materials. This technique allows, in addition, the localization of the compatibilizer in the polymer blends.


1993 ◽  
Vol 26 (11) ◽  
pp. 2771-2778 ◽  
Author(s):  
Gregory T. Dee ◽  
Bryan B. Sauer

2004 ◽  
Vol 856 ◽  
Author(s):  
Tomoko Hashida ◽  
Ying Hua ◽  
Shaw Ling Hsu ◽  
Charles W. Paul

ABSTRACTMorphology development of crystallizable polymer blends has been investigated using optical microscopy, thermal analysis, and vibrational spectroscopy. The blends studied involve crystallizable polyesters of poly(hexamethylene adipate) (PHMA) and poly(hexamethylene sebacate) (PHMS) and non-crystallizable poly(propylene glycol) (PPG). Although these polyesters possess similar chemical structure, they exhibit different phase behavior. Ternary blends including a high glass transition temperature (Tg) component were also studied. Crystallization kinetics in these blends was obtained utilizing Fourier transform infrared spectroscopy. Micro-Raman spectroscopy capable of achieving high spatial resolution (1 μm2) revealed detailed morphological differences in the phase-separated structures. This technique made possible for the first time characterization of the chemical composition of the blends and distribution of crystallites. The role of the third relative immobile component significantly changed both chemical distribution and the degree of crystallinity.


1973 ◽  
Vol 7 (3) ◽  
pp. 525-537 ◽  
Author(s):  
A. W. Neumann ◽  
R. J. Good ◽  
P. Ehrlich ◽  
P. K. Basu ◽  
G. J. Johnston

1991 ◽  
Vol 248 ◽  
Author(s):  
Bryan B. Sauer ◽  
Gregory T. Dee

AbstractSurface tensions of viscous molten polymers were measured with the modified Wilhelmy method. Small diameter fibers were used as vertical surface tension probes giving rise to rapid equilibration of the wetting meniscus. Noise due to thermal convection currents was suppressed by the use of a baffle tube to protect the electro-balance which allowed us to extend our studies to temperatures exceeding 400°C. The precision of the surface tension measurement at T<350°C for n≤10,000 Poise is better than 0.5%. Discussion is made of the rate of meniscus equilibration as a function fiber diameter. The surface tensions of polystyrene(PS), polydimethylsiloxane(PDMS), poly(ethylene glycol)(PEG), poly(propylene glycol)(PPG), and polyethylene(PE) were determined as a function of MW and temperature in order to compare with theoretical predictions. The Cahn-Hilliard interfacial gradient theory is used in conjunction with equation of state models using pressure-volume-temperature data as the input. Good agreement with experiment is found using one adjustable parameter which is independent of MW, for both polar and non-polar polymers.


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