Polyether modified siloxane, coating additive, coating composition, coating agent, coating and preparation method of polyether modified siloxane
A technology of polyether modified siloxane, applied in the field of polyether modified siloxane and coating additives, which can solve the problems of expensive materials and achieve the effect of small environmental load, simple environmental load and excellent antifouling performance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0059]
[0060] Furthermore, the present invention relates to a method for producing a polyether-modified siloxane (siloxane branched polyether-modified silicone) represented by formula (1).
[0061] The method for producing the polyether-modified siloxane of the formula (1) is characterized by including the following step (I) and step (II).
[0062] Process (I): Using the average composition formula (2) (R" 3 SiO 1 / 2 ) g (R” 2 SiO 2 / 2 ) h (R”SiO 3 / 2 ) i (SiO 4 / 2 ) j (In the above formula (2), R" may be the same or different from each other and each independently is a hydroxyl group or a monovalent hydrocarbon group having 1 to 18 carbon atoms, 0≤g≤10, 0≤h≤100, 1≤i ≤30, 0≤j≤8.) The compound represented by the average composition formula (3) (R" 2 SiO 2 / 2 ) k (R”HSiO 2 / 2 ) l The compound represented and / or the average composition formula (4) (R" 3 SiO 1 / 2 ) m (R” 2 HSiO 1 / 2 ) n (R” 2 SiO 2 / 2 ) o (R”HSiO 2 / 2 ) pThe compound represented (in the above fo...
Embodiment 1
[0127] Into the reactor were added 311 g of tris(trimethylsiloxane) methylsilane (compound (2-1)), 4190 g of 1,1,3,3,5,5,7,7-octamethyl After cyclotetrasiloxane (compound (3-1)) and 331 g of 1,3,5,7-tetramethylcyclotetrasiloxane (compound (3-2)), 3.86 g of trifluoromethanesulfonic acid was added acid, reacted at 50°C for 8 hours. After the reaction, the liquid temperature was lowered to 40° C., 23.2 g of KYOWAAD SH-500 (manufactured by Kyowa Chemical Industry Co., Ltd., hydrotalcite) was added and stirred for 1 hour, and the solid content was removed by filtration. Then, the low-boiling components were removed for 5 hours at 150°C / 2torr while bubbling with nitrogen gas, and the organohydrogensiloxane represented by the following average composition formula (5-1) was synthesized in a yield of 87% (step (I). )).
[0128] Next, 97.1 g of the organohydrogensiloxane represented by the average composition formula (5-1) obtained in the step (I) and 79.7 g of the polyoxyalkylene com...
Embodiment 2
[0138] The average composition was synthesized in a yield of 87% in the same manner as in Example 1, except that 163 g of compound (2-1), 4320 g of compound (3-1), and 350 g of compound (3-2) were used in step (I). The organohydrogensiloxane represented by formula (5-2).
[0139] Next, in the step (II), 195 g of the organohydrogensiloxane represented by the average composition formula (5-2) obtained in the step (I) and 169 g of the average composition formula (6-1) were mixed in the reactor. 0.06 g of a 3 mass % isopropanol solution of chloroplatinic acid was added to the obtained mixture, and the mixture was reacted at 80° C. for 4 hours.
[0140] ((CH 3 )3 SiO 1 / 2 ) 3 ((CH 3 ) 2 SiO 2 / 2 ) 109 ((CH 3 )HSiO 2 / 2 ) 10 ((CH 3 )SiO 3 / 2 ) 1 ... average composition formula (5-2)
[0141] After the completion of the reaction, the obtained solution was heated under reduced pressure to distill off the solvent, to obtain an organopolysiloxane compound (polyether-modified s...
PUM
| Property | Measurement | Unit |
|---|---|---|
| dispersity | aaaaa | aaaaa |
| viscosity | aaaaa | aaaaa |
| dispersity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com

