Preparation method of nano silicon dioxide surface-grafted MC nylon composite material
A nano-silica, nylon composite material technology, applied in the field of polymer nano-composite material preparation, can solve the problems of high surface energy, easy agglomeration, poor compatibility, etc., achieve good modulus, overcome easy agglomeration, high strength Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0015] A kind of preparation method of nano silicon dioxide surface grafting MC nylon composite material, carry out according to the following steps:
[0016] a. Add nano-silica to a reaction vessel filled with toluene, protect it with nitrogen, add TDI, after ultrasonication for 30min, add 100ulN, N-dimethylcyclohexylamine, magnetically stir, and react at 40°C for 3h to obtain nano-SiO 2 -g-TDI suspension; mass ratio nano silicon dioxide: TDI=1: 0.8;
[0017] b. Add the toluene solution of caprolactam dropwise to SiO 2 -g-TDI suspension, magnetically stirred, reacted at 90°C for 4 hours, centrifuged to remove the lower layer solution, and vacuum dried to obtain nano-SiO 2 -g-CL;
[0018] c, according to parts by weight, 100 parts of caprolactam and 4 parts of nano-SiO prepared by step b 2 -g-CL was put into the reaction container, after vacuuming for 7min, heated to 90°C to melt the caprolactam, protected by nitrogen, and ultrasonicated for 0.3h to obtain nano-SiO 2 -g-CL...
Embodiment 2
[0022] A kind of preparation method of nano silicon dioxide surface grafting MC nylon composite material, carry out according to the following steps:
[0023] a. Add nano-silica to a reaction vessel filled with toluene, protect it with nitrogen, add TDI, after ultrasonication for 20min, add 50ul N,N-dimethylbenzylamine, stir magnetically, and react at 20°C for 4h to obtain nano-SiO 2 -g-TDI suspension; mass ratio nano silicon dioxide: TDI=1: 0.5;
[0024] b. Add the toluene solution of caprolactam dropwise to SiO 2 -g-TDI suspension, magnetically stirred, reacted at 80°C for 6h, centrifuged to remove the lower layer solution, and vacuum dried to obtain nano-SiO 2 -g-CL;
[0025] c, according to parts by weight, 100 parts of caprolactam and 1.5 parts of nano-SiO prepared by step b 2 -g-CL was put into the reaction container, after evacuating for 5 minutes, heated to 80°C to melt the caprolactam, protected by nitrogen, and ultrasonicated for 0.15h to obtain nano-SiO 2 -g-CL ...
Embodiment 3
[0029] A kind of preparation method of nano silicon dioxide surface grafting MC nylon composite material, carry out according to the following steps:
[0030] a. Add nano-silica to a reaction vessel filled with toluene, protect it with nitrogen, add TDI, after ultrasonication for 40 minutes, add 250ul dioctyltin dioctoate solution, stir magnetically, and react at 60°C for 1 hour to obtain nano-SiO 2 -g-TDI suspension; mass ratio nano silicon dioxide: TDI=1: 1;
[0031] b. Add the toluene solution of caprolactam dropwise to SiO 2 -g-TDI suspension, magnetically stirred, reacted at 100°C for 6h, centrifuged to take the lower layer solution, and vacuum dried to obtain nano-SiO 2 -g-CL;
[0032] c, according to parts by weight, the nano-SiO prepared by 100 parts of caprolactam and 7 parts of b step polymerization 2 -g-CL was put into the reaction container, after vacuuming for 10min, heated to 100°C to melt the caprolactam, protected by nitrogen, and ultrasonicated for 0.5h to ...
PUM
Property | Measurement | Unit |
---|---|---|
tensile strength | aaaaa | aaaaa |
tensile strength | aaaaa | aaaaa |
tensile strength | 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