Unlock instant, AI-driven research and patent intelligence for your innovation.
Fabric treatment
What is Al technical title?
Al technical title is built by PatSnap Al team. It summarizes the technical point description of the patent document.
A technology for fabrics and compositions, applied in fiber processing, textiles and papermaking, etc., can solve problems such as products requiring heat curing
Inactive Publication Date: 2007-09-19
UNILEVER NV
View PDF14 Cites 0 Cited by
Summary
Abstract
Description
Claims
Application Information
AI Technical Summary
This helps you quickly interpret patents by identifying the three key elements:
Problems solved by technology
Method used
Benefits of technology
Problems solved by technology
One of the problems with this method is that the esterification reaction is usually carried out with a sodiumhypophosphite catalyst, and the processed product needs to be thermally cured
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
Click on the blue label to locate the original text in one second.
Reading with bidirectional positioning of images and text.
Smart Image
Examples
Experimental program
Comparison scheme
Effect test
Embodiment 1
[0165] Embodiment 1: the synthesis of butane tetracarboxylic acid two (2,4,6-trichlorophenol esters)
[0166] Weigh butane tetracarboxylic acid (BTCA) (20.84g, 0.089mol) and 2,4,6-trichlorophenol (35.80g, 0.18mol) in a round bottom flask (250cm 3 )middle. The flask was purged with nitrogen for 15 minutes, then distilled THF (150 cm 3 ). After stirring for 30 minutes under nitrogen, diisopropylcarbodiimide (29.0 cm 3 , 0.18mol). The reaction was allowed to proceed overnight with stirring under nitrogen. The mixture was filtered, washed with THF, and stirred for 1 hour to ensure complete precipitation. The crude product was obtained after removal of the solvent. The crude product was washed several times with dichloromethane, and the solvent in the filtrate was removed to obtain the desired product.
Embodiment 2
[0167] Embodiment 2: the synthesis of two (2,4,5-trichlorophenol esters) of succinate
[0168] Succinic acid (1.5g, 0.013mol) was dissolved in DMSO (50cm 3 )middle. 1,1'-Carbonyldiimidazole (5.0 g, 0.03 mol) was added, and the mixture was stirred at room temperature for 30 minutes. Then 2,4,5-trichlorophenol (5.05 g, 0.026 mol) was added, and the mixture was stirred overnight at room temperature. The mixture was poured into water, filtered, washed with water and then with ether to give a white solid (2.03 g, 33%).
[0169] δ H (500MHz; CDCl 3 )3.07 (4H, s, CH 2 -CH 2 -C(O)-O-) and 7.55 & 7.29(4H, s, Ph).
Embodiment 3
[0170] Embodiment 3: the synthesis of succinic acid bis(N-hydroxysuccinimide ester)
[0171] Dissolve succinic acid (2.0 g, 0.017 mol) in THF (50 cm 3 )middle. 1,1'-Carbonyldiimidazole (5.49 g, 0.034 mol) was added, and the mixture was stirred at room temperature for 30 minutes. N-Hydroxysuccinimide (3.89 g, 0.034 mol) was added and the mixture was stirred overnight at room temperature. The mixture was poured into water, filtered, washed with water, and washed with ether to give a white solid (2.0 g, 38%).
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
Property
Measurement
Unit
molecular weight
aaaaa
aaaaa
Login to View More
Abstract
A method of treating finished garments comprising cellulosic material so as to cause cross-linking, which comprises the step of treating fabrics with an effective amount of a blocked cross-linking agent for cellulose, said cross-linking agent being thermally activated. A composition for use in the said method which comprises an effective amount of a blocked cross-linking agent for cellulose, said cross-linking agent being thermally activated.
Description
technical field [0001] The present invention relates to laundry treatment compositions suitable for use in domestic laundry processes, in particular to compositions comprising components capable of crosslinking with cellulose. Background of the invention [0002] Cellulose is a beta-1,4 linked polysaccharide that is the main constituent of cotton, a well known and widely used material in textile production. Cellulose can be cross-linked by hydrogen bonds formed between the cellulose chains. [0003] Most of the clothing purchased around the world contains at least some cellulose fibers in the form of cotton or rayon, and these garments generally experience shrinkage, deformation and wrinkling problem. This phenomenon is thought to be caused by the opening and reformation of hydrogen bonds. [0004] So-called "durable press" treatments of fabrics are used to overcome these problems. One of the most common durable press methods is to fix the cellulose...
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
Application Date:The date an application was filed.
Publication Date:The date a patent or application was officially published.
First Publication Date:The earliest publication date of a patent with the same application number.
Issue Date:Publication date of the patent grant document.
PCT Entry Date:The Entry date of PCT National Phase.
Estimated Expiry Date:The statutory expiry date of a patent right according to the Patent Law, and it is the longest term of protection that the patent right can achieve without the termination of the patent right due to other reasons(Term extension factor has been taken into account ).
Invalid Date:Actual expiry date is based on effective date or publication date of legal transaction data of invalid patent.
Login to View More