A kind of carbon dioxide-based polyurethane amide copolymer and preparation method thereof
A technology of polyurethane amide and carbon dioxide is applied in the field of carbon dioxide-based polyurethane amide copolymer and its preparation.
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[0023] Specific implementation methods (the raw materials are all different, and the different parts have been highlighted)
[0024] The test methods used in the following examples are conventional methods unless otherwise specified, and the raw materials and reagents used, if not otherwise specified, are commercially available raw materials and reagents such as conventional commercial purchases.
[0025] The invention will be further described below in combination with specific embodiments. These examples are only typical descriptions of the present invention, but the present invention is not limited thereto.
Embodiment 1
[0027]
[0028] In a 50ml autoclave, add 5.8g of hexamethylenediamine and 11.4g of caprolactone, and feed N at normal temperature. 2 to 1.0MPa, and then under the conditions of 100°C and 300 rpm, the reaction was completed after 6 hours. After depressurization, directly add 11.6g of hexamethylene dicarbamate to the reaction kettle for transesterification, the temperature is 160°C, and pass N 2 Demethanol, the time is 3h. Then 50 ul of tetrabutyl titanate was added, stirred for 15 minutes, vacuumed, and the temperature was gradually raised to 230°C. Vacuum polycondensation can be done for 2h. The polyurethane amide synthesized above was dissolved in DMSO, and then purified by sedimentation with ethanol. 1-2 g of sample 1 was taken and dissolved in DMSO for NMR analysis. The purified polyurethane amide was pressed into a film, and the tensile strength, elongation at break and impact strength were measured. The results are shown in Table 1.
Embodiment 2
[0030]
[0031] In a 50ml autoclave, add 5.8g of hexamethylenediamine and 11.4g of caprolactone, and feed N at normal temperature. 2 to 1.0MPa, and then under the conditions of 100°C and 300 rpm, the reaction was completed after 6 hours. After depressurization, directly add 13.0g octamethylene dicarbamate to the reaction kettle for transesterification, the temperature is 160°C, and pass N 2 Demethanol, the time is 3h. Then 50 ul of tetrabutyl titanate was added, stirred for 15 minutes, vacuumed, and the temperature was gradually raised to 230°C. Vacuum polycondensation can be done for 2h. The synthesized polyurethane amide was dissolved in DMSO, and then purified by precipitation with ethanol.
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