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Epoxy/castor oil graft interpenetrating polymer networks

✍ Scribed by M.-P. Raymond; V. T. Bui


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
193 KB
Volume
70
Category
Article
ISSN
0021-8995

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✦ Synopsis


Full-interpenetrating polymer networks (IPNs) were prepared from epoxy and castor oil-based polyurethane (PU), by the sequential mode of synthesis and were characterized by different techniques: swelling test, scanning electron microscopy (SEM), thermomechanical analysis (TMA), thermogravimetric analysis (TGA), tensile test, and instrumented impact test. 2,4-Toluene diisocyanate (TDI) was used as a curing agent for castor oil, at a NO/OH ratio Ο­ 1.50. Diglycidyl ether of bisphenol A (DGEBA) was cured and crosslinked using 2,4,6-tris(dimethylaminomethyl)phenol (TDMP) at 1.5%, by weight, of epoxy resin. The homogeneous morphology of IPN samples of PU compositions up to 40%, by weight, revealed by SEM may be attributed to some extent to grafting of the PU phase onto the epoxy matrix, which results from the reaction between NCO groups in the PU phase with OH groups in the epoxy matrix. This has some synergistic effect on the thermal resistance and tensile properties of IPNs compared to those of the pure components, such as illustrated by the data from TGA and tensile tests. However, the grafting structure appears not to enhance their impact resistance, which probably requires the formation of rubbery particles of suitable size.


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A series of interpenetrating polymer networks (IPNs) of polyurethane/polystyrene (PU/PS; 90/10, 75/25, 60/40, and 50/50) have been synthesized by condensation reaction of castor oil with methylene diisocyanate and styrene, employing benzoyl peroxide as initiator. Polystyrene is extracted from IPNs b