Active cross-linking agent, cross-linked polyurethane material as well as preparation method and recovery method thereof
A technology of cross-linked polyurethane and recycling method, which is applied in the field of active cross-linking agent, cross-linked polyurethane material and its preparation method and recycling, which can solve the problem of loss of thermoplastic processing performance, non-compliance with green chemistry and sustainable development, and poor solvent resistance and other issues, to achieve the effect of improved mechanical properties, low cost and high reaction efficiency
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Embodiment 1
[0034] Dissolve 1.001 g of acetylacetone and 0.911 g of 2-amino-1,3-propanediol in 5 mL of tetrahydrofuran, and react at 45°C for 12 hours. The solvent was removed by rotary evaporation, and dried in a vacuum oven at 40° C. for 12 hours to obtain (1,3-dihydroxypropyl-2-yl)-pent-3-en-2-one. figure 1 This is the NMR pattern of (1,3-dihydroxypropyl-2-yl)-pent-3-en-2-one.
Embodiment 2
[0036] 2.002 g of acetylacetone and 0.912 g of 1,3-diamino-2-hydroxypropane were dissolved in 5 ml of ethanol, and reacted at 45° C. for 12 hours. The solvent was removed by rotary evaporation, and dried in a vacuum oven at 40°C for 12 hours to obtain 4,4'-(2-hydroxypropane-1,3-diacyl)bis(malonyl)-bis(pent-3-ene-2- ketone). figure 2 This is the nuclear magnetic spectrum of the 4,4'-(2-hydroxypropane-1,3-diacyl)bis(malonyl)-bis(pent-3-en-2-one).
Embodiment 3
[0038] 0.3464 g of (1,3-dihydroxypropyl-2-yl)-pent-3-en-2-one prepared in Example 1 was dissolved in 20 mL of tetrahydrofuran with 2 g of polytetrahydrofuran and 1.1115 g of IPDI and mixed uniformly. Dry at 60°C for 48 hours, remove the solvent at 100°C and complete the cross-linking reaction. to obtain a cross-linked polyurethane elastomer, image 3 is the stress-strain graph of the crosslinked polyurethane elastomer.
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