Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Amido functional group polysiloxane and composition based on the same

A polysiloxane and group technology, applied in the field of stable compositions with low chloride content, can solve problems such as substances being difficult to dissolve in water

Inactive Publication Date: 2009-01-28
GOLDSCHMIDT CHEM CORP
View PDF16 Cites 12 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But said substances are hardly soluble in water

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Amido functional group polysiloxane and composition based on the same
  • Amido functional group polysiloxane and composition based on the same
  • Amido functional group polysiloxane and composition based on the same

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0131] Condensed by hydrolysis [CH 2 =CH-C 6 h 4 -CH 2 -NH-(CH 2 ) 2 NH(CH 2 ) 3 Si(OCH 3 ) 3 ]HCl(VIb) to prepare amino-functional polysiloxane

[0132] In a heatable 2-1-three-necked flask equipped with a nitrogen stacking device, a distillation device and a dropping funnel, 750 g of a 50% by weight methanol solution of VI (3.74% by weight of silicon) was preliminarily placed. Next, 27 g of water (corresponding to 1.5 mol of water per mol of silicon used) was slowly added with stirring. 27 g of methanol were then removed from the reaction mixture by distillation at ambient pressure. The solution was then heated to 60°C for about 3 hours. The solution had a silicon content of 3.74% by weight.

Embodiment 2

[0134] Condensation by hydrolysis [C 6 h 5 -CH 2 -NH-(CH 2 ) 2 NH(CH 2 ) 3 Si(OCH 3 ) 3 ]HCl(VIc) to prepare functionalized aminopolysiloxane

[0135] Into a heatable 2-1-three-necked flask equipped with a nitrogen stacking device, a distillation device and a dropping funnel, 697 g of a 50% by weight methanol solution of VII (4.01% by weight of silicon) was placed in advance. Next, 27 g of water (corresponding to 1.5 mol of water per mol of silicon used) was slowly added with stirring. 27 g of methanol were then removed from the reaction mixture by distillation at ambient pressure. The solution was then heated to 60°C for about 3 hours. The solution had a silicon content of 4.01% by weight.

Embodiment 3

[0137] NH condensed by hydrolysis 2 -(CH 2 ) 2 NH(CH 2 ) 3 Si(OCH 3 ) 3 (VId) and with CH 2 =CH-C 6 h 4 -CH 2 Preparation of Functionalized Aminopolysiloxane by Reaction of -Cl(VIIa)

[0138] 222 g of aminoethylaminopropyltrimethoxysilane was pre-placed in a heatable 1-1-three-necked flask equipped with a nitrogen stacking device, a reflux cooler and a dropping funnel. Then 27 g of water (corresponding to 1.5 mol per mol of silicon used) were added slowly with stirring. The reaction mixture was heated to about 60°C. The temperature was maintained by heating for 1 hour. Then 105 g of methanol was added. Then 152.5 g of vinylbenzyl chloride mixed with 104.5 g of methanol was slowly added with stirring. The temperature was maintained at 64°C by cooling (during the addition) and subsequent heating for about 3 hours. After cooling, the silicon content was diluted to 3.74% by weight with 138 g of methanol.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
Lengthaaaaaaaaaa
Igniteaaaaaaaaaa
Densityaaaaaaaaaa
Login to View More

Abstract

The invention relates to an amino functional polysiloxane with formulas III and IV, a preparation method thereof and the use as a binder, and the composite based on the amino functional polysiloxane, in particular to the stable chloride-free composite of polysiloxane acidic salt and the preparation and use thereof. The R<1> and R<2> are independent and are respectively expressed by R<1> as -(CH2) pAr<1>, -(CH) pAr<1>, -(CH) pAr<1>-(CHCH2) or -(CH2) pAr<1>-(CHCH2) and / or R<2> as -(CH2) qAr<2>, -(CH) pAr<2>, -(CH) pAr<2>-(CHCH2) or -(CH2) pAr<2>-(CHCH2)-, wherein, p is equal to or more than 0 and equal to or less than 8, q is equal to or more than 0 and equal to or less than 8, and Ar<1> and Ar<2> correspond to aryl, aralkyl or aralkenyl, and n is equal to or more than 1 and equal to or less than 8, m is equal to or more than 1 and equal to or less than 8, Y is the same or different and represents alkoxyl or oxhydryl or O1 / 2; A is inorganic or organic acidic residue and actually exists as T-structure unit, and a is equal to or more than 0 and equal to or less than 2, b is equal to or more than 0 and equal to or less than 1, c is equal to or more than 0, c<*> is equal to or more than c, (a+b) is equal to or more than 0 and equal to or less than 3 and x is equal to or more than 2. The amino functional polysiloxane is also used as the binder between inorganic and organic surfaces or used in the process of coating organic polymer to inorganic surfaces, and the thickness of amino functional polysiloxane layer is less than 800nm.

Description

Technical field: [0001] The present invention consists in aminofunctional polysiloxanes, their preparation and use as binders, and compositions based on aminofunctional polysiloxanes, in particular polysiloxane acid salts with low chloride content Stable composition, method for its preparation and use thereof. Background technique: [0002] Known, such as 3-(N-vinylbenzyl-2-aminoethyl)aminopropyltrimethoxysilane or 3-(N-benzyl-2-aminoethyl)aminopropyltrimethoxysilane Acid salts of functionalized aminosilanes can be used as binders. The use of polyolefins or epoxy resins as binders in the coating of metals, preferably copper and iron, is reported in US4902556, EP353766 and US4849294. According to EP338128, WO8800527, US4499152, US4382991, US4330444, DE2802242 (be applicable to the binder of various resin systems on the glass fiber), EP-A-0845040 or BE845040 (for the binder of the epoxy resin on the flat glass and The technical solution of improving alkali resistance) can r...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C08L83/08
Inventor B·斯坦德克H·劳勒德C·－D·塞勒H·－J·科茨施H·皮特斯P·詹克纳
Owner GOLDSCHMIDT CHEM CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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