2-Acryloylamino-2-methyl-1-propanesulfonic acid (AMPS)-methyl methacrylate (MMA)-halloysite copolymerized denture base material and preparation method thereof
A technology of methyl methacrylate and methylpropanesulfonic acid, which is applied in dental preparations, pharmaceutical formulations, dental prostheses, etc., can solve the problem of low toughness and strength of resin materials, mechanical properties that cannot fully meet oral restorations, and poor impact strength And other issues
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Embodiment 1
[0024] (1) Mix 1.8g AMPS and 58.2g MMA monomers and add them into a three-neck flask (the total amount of monomers is 60mL), add 3gHNTs, ultrasonically disperse the suspension, and add 1.5g hydroxyethyl cellulose to 150mL deionized water at the same time (HEC) and 0.075g sodium dodecylbenzenesulfonate (SDBS), pour it into a three-necked flask after preliminary stirring, and continue stirring at a low speed. Pass N 2 After 40 minutes of protection, the temperature was raised to 90° C., and the inert atmosphere was maintained continuously, and 0.4 g of initiator BPO was added to initiate polymerization. After reacting for 9 hours, the reaction system was cooled and filtered, the filtered product was repeatedly washed with deionized water, and vacuum-dried to a constant weight at 60°C to obtain a P(MMA-co-AMPS) / HNTs nanocomposite;
[0025] (2) Mix the P(MMA-AMPS) / HNTs copolymer product (powder) with the thermosetting tray water at a mass ratio of 1:1, take it out after the mixtu...
Embodiment 2
[0028] (1) Mix 3gAMPS and 57gMMA monomers and add them into a three-necked flask (the total amount of monomers is 60mL), add 0.6gHNTs, and ultrasonically disperse the suspension, and add 1.8g hydroxyethyl cellulose to 150mL deionized water ( HEC) and 0.067g sodium dodecylbenzene sulfonate (SDBS), it is poured into the there-necked flask after initial stirring, and continues stirring at a low speed. Pass N 2After 40 minutes of protection, the temperature was raised to 90° C., and the inert atmosphere was maintained continuously, and 0.4 g of initiator BPO was added to initiate polymerization. After reacting for 9 hours, the reaction system was cooled and filtered, the filtered product was repeatedly washed with deionized water, and vacuum-dried at 60°C to a constant weight to obtain a P(MMA-co-AMPS) / HNTs nanocomposite;
[0029] (2) Mix the P(MMA-AMPS) / HNTs copolymer product (powder) with the thermosetting tray water at a mass ratio of 1:1, take it out after the mixture enters ...
Embodiment 3
[0032] (1) Mix 6gAMPS and 54gMMA monomers and add them into a three-necked flask (the total amount of monomers is 60mL), add 0.9gHNTs, and ultrasonically disperse the suspension, and add 1.6g hydroxyethyl cellulose to 150mL deionized water ( HEC) and 0.075g sodium dodecylbenzene sulfonate (SDBS), it is poured into the there-necked flask after preliminary stirring, and continues stirring at a low speed. Pass N 2 After 40 minutes of protection, the temperature was raised to 90° C., and the inert atmosphere was maintained continuously, and 0.6 g of initiator BPO was added to initiate polymerization. After reacting for 9 hours, the reaction system was cooled and filtered, the filtered product was repeatedly washed with deionized water, and vacuum-dried at 60°C to a constant weight to obtain a P(MMA-co-AMPS) / HNTs nanocomposite;
[0033] (2) Mix the P(MMA-AMPS) / HNTs copolymer product (powder) with the thermosetting tray water at a mass ratio of 1:1, take it out after the mixture en...
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