Heat-curable polyurethane resin composition and urethane elastomer molded article using the same
A polyurethane resin and polyurethane prepolymer technology, which is applied in the field of polyurethane elastomer moldings, can solve the problems of deterioration of compression set resistance, difficulty in obtaining flame-retardant and low-hardness polyurethane elastomer moldings, etc., and achieve compression resistance Excellent permanent deformation effect
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[0070] Hereinafter, the present invention will be explained in more detail through examples, but the scope of the present invention is not limited to these examples.
[0071] In addition, in the present invention, unless otherwise specified, "parts" are "parts by mass" and "%" are "mass%".
Synthetic example 1
[0072] Synthesis Example 1 Synthesis of polyurethane prepolymer (D-1) with blocked isocyanate groups
[0073] While stirring vigorously, add 74 parts of 2,4-toluene diisocyanate (NCO / OH = 1.7) to 500 parts of polytetramethylene ether glycol ("PTMG-2000" manufactured by Mitsubishi Chemical Corporation, number average molecular weight 2000) ), react at 100°C for 4 hours to obtain a polyurethane prepolymer.
[0074] This polyurethane prepolymer was cooled to 60°C, 31 parts of methyl ethyl ketoxime as a blocking agent was put into it, stirred at 70°C for 2 hours and reacted, thereby obtaining a polyurethane prepolymer with blocked isocyanate groups (D-1) . The obtained isocyanate group blocked polyurethane prepolymer (D-1) had a viscosity of 3800 mPa·s at 80°C.
Synthetic example 2
[0075] Synthesis Example 2 Synthesis of polyurethane prepolymer (D-2) with blocked isocyanate groups
[0076] While vigorously stirring, into 500 parts of liquid polyester diol (polyester diol obtained from 3-methylpentanediol and adipic acid, molecular weight 2000) was added 74 parts of 2,4-toluene diisocyanate (NCO / OH=1.7) and reacted at 100°C for 4 hours to obtain a polyurethane prepolymer.
[0077] This polyurethane prepolymer was cooled to 60°C, 31 parts of methyl ethyl ketoxime as a blocking agent was put into it, stirred at 70°C for 2 hours and reacted, thereby obtaining a polyurethane prepolymer with blocked isocyanate groups (D-2) . The obtained polyurethane prepolymer (D-2) in which the isocyanate group was blocked had a viscosity at 80°C of 4200 mPa·s.
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