Hardenable composition
A technology of curable composition and cured product, which is applied in the direction of polyether adhesives, adhesive types, adhesives, etc., and can solve the problem of polyether polymers with insufficient weather resistance, heat resistance, and low degree of freedom in blending ratio , poor compatibility, etc., to achieve excellent weather resistance and heat resistance, improve curing and brittle properties, and high bonding strength
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[0578] Hereinafter, examples and comparative examples of the present invention will be described, but the present invention is not limited to the following examples.
[0579] "Parts" and "%" in the following synthesis examples, examples, and comparative examples represent "parts by weight" and "% by weight", respectively.
[0580] The synthesis example of the polymer of this invention is shown below.
[0581] In the following synthesis examples, "number average molecular weight" and "molecular weight distribution (ratio of weight average molecular weight to number average molecular weight)" were calculated in terms of standard polystyrene using gel permeation chromatography (GPC). Among them, a polystyrene cross-linked gel-packed column (shodex GPC K-804, manufactured by Showa Denko) was used as a GPC column, and chloroform was used as a GPC solvent.
[0582] Synthesis of Poly(n-Butyl Acrylate) Polymers with Crosslinkable Silyl Groups
Synthetic example 1
[0584] In nitrogen atmosphere, add CuBr (1.09kg), acetonitrile (11.4kg), butyl acrylate (26.0kg) and 2,5-dibromoadipate (2.28kg) in 250L reactor, in 70 Stir at ~80°C for about 30 minutes. Pentamethyldiethylenetriamine was added thereto to start the reaction. Butyl acrylate (104 kg) was continuously added for 2 hours after 30 minutes from the start of the reaction. During the reaction, pentamethyldiethylenetriamine is appropriately added so that the internal temperature is 70°C to 90°C. The total amount of pentamethyldiethylenetriamine used so far was 220 g. After 4 hours from the start of the reaction, volatile components were removed by heating and stirring at 80°C under reduced pressure. Acetonitrile (45.7 kg), 1,7-octadiene (14.0 kg), and pentamethyldiethylenetriamine (439 g) were added thereto, and stirring was continued for 8 hours. For the mixture, volatile components were removed by heating and stirring at 80°C under reduced pressure.
[0585] Toluene is added to t...
Synthetic example 2
[0592]In a nitrogen atmosphere, CuBr (1.21kg), acetonitrile (10.8kg), butyl acrylate (7.19kg), ethyl acrylate (10.3kg), 2-methoxyethyl acrylate (8.47kg ) and 2,5-dibromodiethyl adipate (3.37kg), heated and stirred at 70-80°C for about 30 minutes. Pentamethyldiethylenetriamine was added thereto to start the reaction. A mixture of butyl acrylate (28.8 kg), ethyl acrylate (41.3 kg), and 2-methoxyethyl acrylate (33.9 kg) was continuously added for 2 hours from 30 minutes after the start of the reaction. During the reaction, pentamethyldiethylenetriamine is appropriately added so that the internal temperature is 70°C to 90°C. The total amount of pentamethyldiethylenetriamine used so far was 243 g. After 4 hours from the start of the reaction, volatile components were removed by heating and stirring at 80°C under reduced pressure. Acetonitrile (32.5 kg), 1,7-octadiene (30.9 kg), and pentamethyldiethylenetriamine (486 g) were added thereto, and stirring was continued for 4 hours. ...
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