Thermoplastic polyurethane resin for melt spinning
A technology of polyurethane urea and resin, applied in the field of manufacturing this thermoplastic polyurethane resin, thermoplastic polyurethane urea resin
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Embodiment I
[0085] Polybutylene adipate (PBHA, Mw=1,000), a polyol, was dried in a vacuum oven at 120° C. for 5 hours so that the water content of the raw material for preparing the preester was 150 ppm or less. Melt methane diphenyl-4,4'-diisocyanate (MDI) in a 45°C oven.
[0086] A round-bottomed cylindrical reactor configured with a controllable stirrer is placed in an oil bath maintained at 90° C., and diisocyanate and polyol (equivalent ratio: diisocyanate: polyol=1.80:1.00) are put into the reactor mixture. In the presence of 10-100 ppm organotin catalyst such as T-10, react for 5 minutes or longer while stirring at 1,000 rpm to obtain a prepolymer. The progress of the reaction to prepare the prepolymer was monitored by monitoring the current change on the stirrer motor, which was found to reach a maximum point after 2 minutes of stirring.
[0087] To provide the prepolymer with amine functionality, 0.80 equivalents of water were added with stirring. This reaction produces CO 2 ...
Embodiment II
[0090] Repeat the steps of Example 1, using MDI with an equivalent ratio of 1.80: 1.0: 0.80: PBHA-1500: H 2 O. The physical properties of the polymer obtained are listed in Table 1 below.
Embodiment III
[0092] The same steps as in Example 1 were repeated, except that polybutylene ether glycol (PTMG, Mw=1,000) was used as the polyol, and MDI:PTMG-1000:H with an equivalent ratio of 1.80:1.0:0.80 was used. 2 O. The physical properties of the polymer obtained are listed in Table 1 below.
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