Degradable thermoplastic elastomer and preparation method thereof
A thermoplastic elastomer and elastomer technology, applied in the field of degradable materials, can solve the problems of uneven particle agglomeration and dispersion, easy agglomeration of inorganic nanoparticles, and unsatisfactory interface compatibility, so as to improve mechanical properties and promote two-phase phase. The effect of volume and good resilience
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Embodiment 1
[0035] Add 50 parts of PBAT pellets, 5 parts of PCL pellets, and 100 parts of dichloromethane into the reaction vessel, stir magnetically at room temperature for 6 hours, then add 1 part of glycidyl etheroxypropyl cyclotetrasiloxane, and 0.1 part of ammonium hydroxide , and continued magnetic stirring at room temperature for 3 h. After the reaction was finished, the dichloromethane solvent was removed by rotary evaporation under negative pressure conditions, washed 3 times with absolute ethanol, and dried at low temperature to obtain the product glycidyl etheroxypropyl cyclotetrasiloxane-g-PBAT / PCL (reactant and The molecular structure of the product is as figure 1 shown).
Embodiment 2
[0037] Add 50 parts of PBAT pellets, 5 parts of PCL pellets, and 100 parts of dichloromethane into the reaction vessel, stir magnetically at room temperature for 6 hours, then add 1 part of epoxycyclohexylethyl clathrate polysilsesquioxane, and hydrate 0.1 part of ammonium, and continued magnetic stirring at room temperature for 4 h. After the reaction was finished, the dichloromethane solvent was removed by rotary evaporation under negative pressure conditions, washed 3 times with absolute ethanol, and dried at low temperature to obtain the product epoxycyclohexylethyl clathrate polysilsesquioxane-g-PBAT / PCL ( The molecular structures of the reactants and products are figure 2 shown).
Embodiment 3
[0039] Add 50 parts of PBAT pellets, 5 parts of PCL pellets, and 100 parts of dichloromethane into the reaction vessel, stir magnetically for 6 hours at room temperature, and then add 1 part of trapezoidal polysilsesquioxane whose side group is glycidyl etheroxypropyl , 0.1 part of ammonium hydroxide, and continued magnetic stirring at room temperature for 5 h. After the reaction was finished, the dichloromethane solvent was removed by rotary evaporation under negative pressure conditions, washed with absolute ethanol 3 times, and dried at low temperature to obtain the product trapezoidal polysilsesquioxane-g-PBAT / PCL (molecular structure formula of reactant and product like image 3 shown).
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