Curing agent 4,4'-biphenyl methane diisocyanate prepolymer and preparation method thereof
A technology of diphenylmethane and diisocyanate, applied in 4 fields, can solve the problems of not being able to produce high solid content products, unable to meet the extensive demand for performance, single variety of coating curing agents, etc. The effect of improved performance and low toxicity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0040] a. Add 100 grams of molten 4,4,-diphenylmethane diisocyanate and 100 grams of ethyl acetate into the reaction kettle, stir evenly, heat up to 65°C, and add polyethylene adipate glycol dehydrated by vacuum 120 g of propylene glycol ester diol was reacted at 60-70° C. for 2 hours and at 90-100° C. for 1 hour to prepare the modified MDI. b. Under stirring, add dropwise a mixture of 12 grams of trimethylolpropane and 12 grams of ethyl acetate to the reaction kettle at a temperature of 80-90°C, drop it in 2 hours, keep it warm for 1 hour, and then rise Heat the reaction at 90-100°C for 2 hours, then lower the temperature to 60°C. C, add 120 gram ethyl acetate solvents by product solid content requirement, stir, the MDI curing agent that 464 gram solid content is 50% is obtained in discharging, the NCO content of this curing agent is 5.7% (calculated as total solid) after testing 11.4%).
[0041] (Note: 1. The detection of solid content is carried out according to the natio...
Embodiment 2
[0044] a. Add 220 grams of molten 4,4,-diphenylmethane diisocyanate and 50 grams of ethyl acetate in the reaction kettle, stir well, heat up to 65°C, add 30 grams of polyoxypropylene glycol dehydrated by vacuum , react at 70-80°C for 2 hours, and react at 90-100°C for 1 hour to prepare the MDI modified product. b. Under stirring, add dropwise a mixture of 35 grams of trimethylolpropane and 35 grams of ethyl acetate to the reaction kettle at a temperature of 80-90°C, drop it in 1 hour, keep it warm for 3 hours, and then raise Heat the reaction at 90-100°C for 4 hours, then lower the temperature to 60°C. c. Add 10 grams of ethyl acetate solvent according to the solid content of the product, stir evenly, and discharge 380 grams of MDI curing agent with a solid content of 75% and a viscosity of 1800mpa.s (25°C). The NCO content of the curing agent is detected. was 8.4%.
[0045] (Note: The detection viscosity is carried out according to the national standard "GB / T2794-1995 Deter...
Embodiment 3
[0047] a. Add 200 grams of molten 4,4,-diphenylmethane diisocyanate and 50 grams of ethyl acetate to the reactor, stir well, heat up to 65°C, and add 30 grams of polyoxypropylene glycol dehydrated by vacuum , react at 80-90°C for 1 hour, then add 30 grams of polyethylene adipate propylene glycol ester diol that has been vacuum-dehydrated, react at 80-90°C for 1 hour, and react at 90-100°C for 2 hours , to prepare MDI modified products. b. Under stirring, add dropwise a mixture of 31 grams of trimethylolpropane and 31 grams of ethyl acetate to the reaction kettle at a temperature of 80-90°C, drop it in 3 hours, keep it warm for 2 hours, and then rise Heat the reaction at 90-100°C for 2 hours, then lower the temperature to 60°C. c. Add 16 grams of ethyl acetate solvent according to the solid content requirements of the product, stir evenly, and discharge to obtain 388 grams of MDI curing agent with a solid content of 75% and a viscosity of 2300mpa.s (25°C).
PUM
Property | Measurement | Unit |
---|---|---|
viscosity | aaaaa | aaaaa |
viscosity | aaaaa | aaaaa |
impact 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