Organic/inorganic nano hybridized hydrogel for tooth root canal filling material
A filling material, inorganic nanotechnology, applied in dentistry, dental preparations, dental prostheses, etc., can solve the problems of coronal leakage and root canal treatment failure, improve the mechanical properties of gel, eliminate micro-gap and coronal Leakage phenomenon, the effect of easy inspection
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0023] Add 200ml of a mixture of ethanol and deionized water (volume ratio 95:5) into the three-neck flask to adjust the pH to 3-4, then add 50g of silane coupling agent A174, and hydrolyze for 3 hours at room temperature. 10 g of inorganic nanoparticles (ZnO:ZrO 2 =50:1) was dispersed in 200ml of deionized water, added to a three-neck flask, ultrasonicated at 70°C for 1 hour, then slowly added dropwise 5g of the silane coupling agent solution prepared in the above hydrolysis within 30 minutes, and then adjusted the pH value of the solution to 9 -11, continue to react for 3 hours under ultrasonic conditions at 70°C. After the modification, ethanol solution is used to elute the unreacted silane coupling agent, and the modified inorganic nano antibacterial powder is obtained after drying. Take 0.1g of the modified inorganic nanopowder, disperse it into 10ml of deionized water, stir well, add 0.5g of N-isopropylacrylamide, pass N 2 After 30 minutes, add 0.01g of N,N'-methyleneb...
Embodiment 2
[0025] Add 200ml of a mixture of ethanol and deionized water (volume ratio 95:5) into the three-neck flask to adjust the pH to 3-4, then add 50g of silane coupling agent A151, and hydrolyze for 3 hours at room temperature. 10 g of inorganic nanoparticles (ZnO:ZrO 2 =50:1) was dispersed in 200ml of deionized water, added to a three-necked flask, ultrasonicated at 70°C for 1 hour, then slowly added dropwise 5g of the silane coupling agent solution prepared in the above hydrolysis step within 30 minutes, and then the pH value of the solution was adjusted to 9-11, the reaction was continued for 3 hours under ultrasonic conditions at 70°C. After the modification, ethanol solution is used to elute the unreacted silane coupling agent, and the modified inorganic nano antibacterial powder is obtained after drying. Take 0.1g of the modified inorganic nanopowder, disperse it into 10ml of deionized water, stir well, add 2g of N-isopropylacrylamide, pass N 2 After 30 minutes, add 0.02g ...
Embodiment 3
[0027] Add 200ml of a mixture of ethanol and deionized water (volume ratio 95:5) into the three-neck flask to adjust the pH to 3-4, then add 50g of silane coupling agent A174, and hydrolyze for 3 hours at room temperature. 10 g of inorganic nanoparticles (ZnO:ZrO 2 =80:1) was dispersed in 200ml of deionized water, added to a three-necked flask, ultrasonicated for 1 hour at 70°C, and then slowly added dropwise within 30 minutes 5 g of the silane coupling agent solution prepared in the above hydrolysis step, and then the pH value of the solution was adjusted to 9-11, the reaction was continued for 3 hours under ultrasonic conditions at 70°C. After the modification, ethanol solution is used to elute the unreacted silane coupling agent, and the modified inorganic nano antibacterial powder is obtained after drying. Take 1g of the modified inorganic nanopowder, disperse it into 10ml of deionized water, stir well and add 0.5g of N-methylolacrylamide, pass N 2 After 30 minutes, add ...
PUM
Property | Measurement | Unit |
---|---|---|
particle diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com