Segmented Polyurethane Elastomers with Liquid Crystalline Hard Segments. 1. Synthesis and Phase Behavior

1994 ◽  
Vol 27 (10) ◽  
pp. 2814-2819 ◽  
Author(s):  
Weiming Tang ◽  
Richard J. Farris ◽  
William J. MacKnight ◽  
Claus D. Eisenbach
1976 ◽  
Vol 49 (1) ◽  
pp. 64-84 ◽  
Author(s):  
Thor L. Smith

Abstract The discussion in this paper has been focused on the strength of Polyurethane elastomers, data on other materials being presented for comparison and to illustrate factors that affect strength. Although the literature on Polyurethane elastomers is voluminous, only in recent years has it been widely recognized that plastic domains exist in most polyurethane formulations of technological importance. Evidence for domain formation and aspects of domain morphology are discussed in recent reviews. The morphology of domains in segmented polyurethane elastomers is more complex than of those in triblock elastomers and has not been studied extensively, although progress is being made, indicated by the discussions in recent publications and references cited therein. In view of the complexities of fracture and the limited information on the morphology and time-dependent mechanical properties of polyurethane elastomers, only general relations between strength and chemical structure have thus far been established. On the other hand, useful correlations can be established by considering the type, size, and concentration of the hard segments and whether strain-induced crystallization is a dominant factor.


1995 ◽  
Vol 28 (2) ◽  
pp. 512-516 ◽  
Author(s):  
Wolfgang Wedler ◽  
Weiming Tang ◽  
H. Henning Winter ◽  
William J. MacKnight ◽  
Richard J. Farris

Author(s):  
Md. Hamidul Kabir ◽  
Ravshan Makhkamov ◽  
Shaila Kabir

The solution properties and phase behavior of ammonium hexylene octyl succinate (HOS) was investigated in water and water-oil system. The critical micelle concentration (CMC) of HOS is lower than that of anionic surfactants having same carbon number in the lipophilic part. The phase diagrams of a water/ HOS system and water/ HOS/ C10EO8/ dodecane system were also constructed. Above critical micelle concentration, the surfactant forms a normal micellar solution (Wm) at a low surfactant concentration whereas a lamellar liquid crystalline phase (La) dominates over a wide region through the formation of a two-phase region (La+W) in the binary system. The lamellar phase is arranged in the form of a biocompatible vesicle which is very significant for the drug delivery system. The surfactant tends to be hydrophilic when it is mixed with C10EO8 and a middle-phase microemulsion (D) is appeared in the water-surfactant-dodecane system where both the water and oil soluble drug ingredient can be incorporated in the form of a dispersion. Hence, mixing can tune the hydrophile-lipophile properties of the surfactant. Key words: Ammonium hexylene octyl succinate, mixed surfactant, lamellar liquid crystal, middle-phase microemulsion. Dhaka Univ. J. Pharm. Sci. Vol.3(1-2) 2004 The full text is of this article is available at the Dhaka Univ. J. Pharm. Sci. website


Polymers ◽  
2021 ◽  
Vol 13 (13) ◽  
pp. 2060
Author(s):  
Shazia Naheed ◽  
Mohammad Zuber ◽  
Mahwish Salman ◽  
Nasir Rasool ◽  
Zumaira Siddique ◽  
...  

In this study, we evaluated the morphological behavior of polyurethane elastomers (PUEs) by modifying the soft segment chain length. This was achieved by increasing the soft segment molecular weight (Mn = 400–4000 gmol−1). In this regard, polycaprolactone diol (PCL) was selected as the soft segment, and 4,4′-cyclohexamethylene diisocyanate (H12MDI) and 1,6-hexanediol (HDO) were chosen as the hard segments. The films were prepared by curing polymer on Teflon surfaces. Fourier transform infrared spectroscopy (FTIR) was utilized for functional group identification in the prepared elastomers. FTIR peaks indicated the disappearance of −NCO and −OH groups and the formation of urethane (NHCOO) groups. The morphological behavior of the synthesized polymer samples was also elucidated using scanning electron microscopy (SEM) and atomic force microscopy (AFM) techniques. The AFM and SEM results indicated that the extent of microphase separation was enhanced by an increase in the molecular weight of PCL. The phase separation and degree of crystallinity of the soft and hard segments were described using X-ray diffraction (XRD). It was observed that the degree of crystallinity of the synthesized polymers increased with an increase in the soft segment’s chain length. To evaluate hydrophilicity/hydrophobicity, the contact angle was measured. A gradual increase in the contact angle with distilled water and diiodomethane (38.6°–54.9°) test liquids was observed. Moreover, the decrease in surface energy (46.95–24.45 mN/m) was also found to be inconsistent by increasing the molecular weight of polyols.


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