Polysiloxane copolymer, antistatic agent and resin composition containing same
A resin composition, polysiloxane technology, applied in other chemical processes, chemical instruments and methods, etc., can solve the problem that the silicone resin has no heat resistance, the curing reaction of the silicone resin is not fully carried out, and the strength characteristic cannot be obtained. Resin composition and other problems, to achieve the effect of excellent heat resistance and high antistatic performance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment
[0095] Next, the present invention will be specifically described based on examples, but the present invention is not limited by these examples.
[0096] In the examples, the surface resistivity was measured under the conditions of 23±3° C. and humidity of 45±5% using Hirester UP (MCP-HT450) manufactured by Mitsubishi Chemical Corporation.
[0097] In addition, regarding heat resistance evaluation, using TG / DTA220 manufactured by Seiko Instruments Co., Ltd., in the measurement results of TG-DTA measured under a nitrogen atmosphere and a temperature increase of 10°C / min, the temperature at which 5% of the mass is reduced Set as the decomposition temperature. When the decomposition temperature is 300°C or higher, it is considered to have heat resistance that can be melt-kneaded in polycarbonate resin, and the evaluation is "A". Adequate with a "C" rating.
manufacture example 1
[0099] In a 500 mL glass reactor equipped with a stirring device, 130.3 g (1.1 mol) of dimethyldimethoxysilane, 42.20 g (0.31 mol) of methyltrimethoxysilane, and 136.3 g of isopropanol were charged under a nitrogen atmosphere. g and 1-(3-trimethoxysilylpropyl)-1,1,1-tributylphosphonium=bis(trifluoromethanesulfonyl) produced by the method described in JP-A-2010-248165 ) imine 100.0 g (0.15 mol). After adding 30.00 g of 0.1N hydrochloric acid dropwise to the obtained mixture at room temperature, it was further stirred at room temperature for 16 hours, and the obtained reaction mixture was concentrated at 80° C. for 4 hours using a rotary evaporator. The obtained concentrated residue was liquid-separated and washed twice with 272.5 g of n-hexane, and then concentrated at 80° C. for 5 hours using a rotary evaporator to obtain 120.2 g of polysiloxane copolymer A as a white suspension liquid.
manufacture example 2
[0101] Except having used 45.90 g (0.31 mol) of vinyltrimethoxysilanes instead of methyltrimethoxysilane, it carried out similarly to manufacture example 1, and obtained the polysiloxane copolymer B123.10g of white suspension liquid.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


