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

Compositions comprising quat compounds and organopolysiloxanes

A technology of polysiloxane and siloxane copolymer, which is applied in the directions of organic cleaning compositions, softening compositions, detergent compositions, etc., can solve the problems of complex synthesis sequence and the like

Inactive Publication Date: 2013-08-21
WACKER CHEM GMBH
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This synthetic sequence is relatively complex and must be carried out at high temperature (200°C) for many hours (3-8h), i.e. somewhat unattractive

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
  • Compositions comprising quat compounds and organopolysiloxanes
  • Compositions comprising quat compounds and organopolysiloxanes

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0194] 119 g of an alkyl-ketene dimer (alkyl R about 16 carbon atoms, commercially available as "AKD" from Trigon Chemie GmbH) having a diketene equivalent of 570 g / mole were carefully melted without overheating . At 63°C, with cooling and efficient stirring, 21.4 g of 3-dimethylaminopropylamine were gradually metered in so that the internal temperature of 75°C was not exceeded. A few minutes after the spray addition was complete, the amidation was complete. The amidoamine was obtained with an amine number of 1.48 (theoretical 1.49), indicating practically 100% yield.

[0195] The amidoamine obtained is heated to 100° C. and a total of 37.2 g of methyl p-toluenesulfonate (0.95 moles per mole of tertiary amino groups in the amidoamine) are added within a period of 30 minutes. The system was reacted for an additional 2 hours at 100° C. to obtain 177.6 g of dialkylacetoacetamidoquaternary ammonium, which solidified on cooling. The product has an amine number of 0.07, which cor...

Embodiment 2

[0197] 119 g of the alkyl-ketene dimer described in Example 1 (570 g / mole of diketene) was mixed with a total of 39.2 g of bis(3-dimethylaminopropyl)amine (under the trade name "JEFFCAT Z130" commercially available from Huntsman) was gradually mixed. Shortly after capping the sparged end, the exothermic amidation reaction was complete. Afterwards, the amidoamine obtained was mixed with 74.5 g of methyl p-toluenesulfonate (0.95 mol per mole of tertiary amino groups in the amidoamine) at 100° C., added a little at a time, while the reaction mixture reached 118° C. . The reaction was allowed to complete at 100°C over the course of 2 hours. Based on an amine number of 0.11, about 94% of the tertiary amino groups are quaternized.

[0198] Production of emulsion (A) from the β-ketocarbonyl quaternary ammoniums of the invention:

[0199] 5.0 g of the β-ketocarbonyl quaternary ammonium (AKD Quat1) obtained in the examples were carefully melted in a glass beaker and mixed with 0....

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
molecular weightaaaaaaaaaa
viscosityaaaaaaaaaa
viscosityaaaaaaaaaa
Login to View More

Abstract

Novel compositions are described, comprising (1) beta-ketocarbonyl quat compounds which contain one or more beta-ketocarbonyl groups of the general formula (I): R-CH2-(C=O)-CHR-(C=O)- and one or more quaternary ammonium groups, where R may be the same or different and is an aliphatic hydrocarbonyl radical having 6 to 28 carbon atoms, and (2) organopolysiloxanes or siloxane copolymers which are liquid at 25 DEG C and 1020 hPa.

Description

technical field [0001] The present invention relates to compositions comprising quaternary ammoniums and organopolysiloxanes and their use in fabric conditioners. Background technique [0002] EP1259672B1 describes the use of alkyl-ketene dimer dispersions (dispersions) for anti-crease finishing of textiles. Cationic emulsifiers prepared by partial reaction from alkyl-ketene dimers and polyethyleneimines are also described. Apart from these partial reaction products in which some of the amino groups of the polyethyleneimine are amidated, the dispersed alkyl-ketene dimer remains intact and ends up on the fiber as such. The quaternization of partially converted polyethyleneimine emulsifiers has not been described and is hardly economical because of the high percentage of primary and secondary amino groups. [0003] Alkyl-ketene dimer dispersions useful as textile auxiliaries are described in the following documents: [0004] CH388246 describes the use of formulations (formu...

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): C08J5/02C07C225/06C11D3/37C08L83/04C08J3/03
CPCC08K5/07C08L83/04C11D1/62C11D3/0015C11D3/3738C07C225/06C11D3/37C11D3/001C11D3/0036
Inventor 克里斯蒂安·赫尔齐格理查德·贝克尔伊娃·鲍曼
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