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

Organosilicon compounds and the use thereof for producing hydrophilic surfaces

A technology for compounds and cross-linked compositions, applied in the fields of materials, formulations, and production of hydrophilic surfaces, can solve the problems of by-products that must be removed, unavailable, expensive feedstocks, etc.

Inactive Publication Date: 2015-01-07
WACKER CHEM GMBH
View PDF9 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0019] Production methods for the aforementioned compounds have the disadvantage of using unavailable and / or expensive feedstocks, or having to remove by-products

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
  • Organosilicon compounds and the use thereof for producing hydrophilic surfaces
  • Organosilicon compounds and the use thereof for producing hydrophilic surfaces
  • Organosilicon compounds and the use thereof for producing hydrophilic surfaces

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0134] Production (Product 1)

[0135] (CH 3 O) 3 Si-CH 2 CH 2 CH 2 OCH 2 CH(OH)CH 2 OC(=O)CH 2 -O(CH 2 CH 2 O) 2-6 -(CH 2 ) 11-13 CH 3 with

[0136] (CH 3 O) 3 Si-CH 2 CH 2 CH 2 OCH 2 CH(CH 2 OH)OC(=O)CH 2 -O(CH 2 CH 2 O) 2-6 -(CH 2 ) 11-13 CH 3

[0137] In a glass flask with a Lebig condenser and receiver, 100 g of glycolic acid ethoxylated lauryl ether (Mn=460 g / mol) (as AKYPO RLM 45CA from KAO Chemicals GmbH, Emmerich, Germany) Obtained) Stir at 100°C and 20 mbar until no further separation of water occurs. After the nitrogen gas was introduced, 47g of (3-glycidoxypropyl)trimethoxysilane (in the trade name GF 80, commercially available from Wacker Chemie AG, Munich, Germany) and 0.5 g of 1,4-diazabicyclo[2.2.2]octane (as Commercially available from Sigma-Aldrich Chemie GmbH, Taufkirchen, Germany), and it was stirred at 100°C for two hours. Cooling and filtering yielded 135 g of slightly yellow liquid. 13 C NMR and titration showed more than 80% adduct formation.

[0138] 1g of...

Embodiment 2

[0140] Production (Product 2)

[0141] (EtO) 3 Si-CH 2 CH 2 CH 2 OCH 2 CH(OH)CH 2 OC(=O)CH 2 -O(CH 2 CH 2 O) 5-9 -Iso-C 13 H 27 with

[0142] (EtO) 3 Si-CH 2 CH 2 CH 2 OCH 2 CH(CH 2 OH)OC(=O)CH 2 -O(CH 2 CH 2 O) 5-9 -Iso-C 13 H 27

[0143] In a glass flask with a Lebig condenser and receiver, 100 g of glycolic acid ethoxy isotridecyl ether (Mn=570 g / mol) (as Marlowet 4538, available from Sasol Germany GmbH, Hamburg, Germany) Commercially available) Stir at 100°C and 20 mbar until no further water separation occurs. After the nitrogen gas was introduced, 45g of (3-glycidoxypropyl)trimethoxysilane (in the trade name GF 82, commercially available from Wacker Chemie AG, Munich, Germany) and 0.5 g of 1,4-diazabicyclo[2.2.2]octane (as Commercially available from Sigma-Aldrich Chemie GmbH, Taufkirchen, Germany), and it was stirred at 100°C for two hours. Cooling and filtering yielded 137 g of slightly yellow liquid. 13 C NMR and titration showed more than 80% adduct formation.

[0144] ...

Embodiment 3

[0146] Production (Product 3)

[0147] (EtO) 3 Si-CH 2 CH 2 CH 2 OCH 2 CH(OH)CH 2 OC(=O)CH 2 -O(CH 2 CH 2 O) 3-7 -(CH 2 ) 8 CH=CH(CH 2 ) 5-7 CH 3 ,

[0148] with

[0149] (CH 3 O) 3 Si-CH 2 CH 2 CH 2 OCH 2 CH(CH 2 (OH))OC(=O)CH 2 -O(CH 2 CH 2 O) 3- 7 -(CH 2 ) 8 CH=CH(CH 2 ) 5-7 CH 3

[0150] In a glass flask with a Lebig condenser and receiver, 105 g of glycolic acid ethoxy oleyl ether (Mn=540 g / mol) (as AKYPO RO 50VG, available from KAO Chemicals GmbH, Emmerich, Germany) Commercially available) Stir at 100°C and 20 mbar until no further water separation occurs. After the nitrogen gas was introduced, 43g of (3-glycidoxypropyl)trimethoxysilane (in the trade name GF 80, commercially available from Wacker Chemie AG, Munich, Germany) and 0.5 g of 1,4-diazabicyclo[2.2.2]octane (as Commercially available from Sigma-Aldrich Chemie GmbH, Taufkirchen, Germany), and it was stirred at 100°C for two hours. Cooling and filtering produced 138 g of a cloudy and yellowish liquid. 13 C NMR and ti...

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

No PUM Login to View More

Abstract

Organosilicon compounds used for production of hydrophilic surfaces are prepared via an addition reaction of epoxy-functional silanes onto polyethylene glycols, cross-linked via a condensation reaction, and used for modification of substrate surfaces such as hardened silicone elastomers, glass surfaces, surfaces of silicatic construction materials, metals, and plastics.

Description

Technical field [0001] The present invention relates to organosilicon compounds, methods for the production of these compounds, and the use of these compounds in the production of hydrophilic surfaces, and preferably relates to compositions and preparations that contain the compounds or have been coated with the compounds , And materials. Background technique [0002] The production of hydrophilic surfaces is expected in many sectors. In the case of building materials and building aids, in order to reduce droplet formation, a hydrophilic surface may be desirable for faster outflow (runoff) and condensation of water, thereby for faster drying, and to avoid scale deposits And avoid residues from water. The hydrophilic surface prevents fogging of optical components, glasses, and windows. In the case of silicone, the hydrophilic surface can delay the adhesion of microbial flora and salt deposits (salt beds), and the contamination of organic matter. The hydrophilic surface improve...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C07F7/08C07F7/18C08J7/12
CPCC07F7/1836C09D183/06C08G77/14C08G77/18C07F7/0818C07F7/081C07F7/1804
Inventor 马尔科·普拉瑟乌韦·施姆
Owner WACKER CHEM GMBH
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