Al technical title is built by PatSnap Al team. It summarizes the technical point description of the patent document.
A direct, p-nitrotoluene technology, applied in the direction of organic dyes, stilbene-azo dyes, etc., can solve the problem of low dyeing rate
Active Publication Date: 2015-01-28
常州悦朋科技有限公司
View PDF4 Cites 2 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
Its advantage is that the price is low, but its dyeing rate is low, so it is
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
preparation example Construction
[0016] A kind of preparation method of environment-friendly direct yellow 11 with high dye uptake rate, its preparation comprises the following process:
[0017] 4) Weigh diethylene glycol ethyl ether in a three-necked flask, weigh p-nitrotoluene o-sulfonic acid and add it, after stirring evenly, weigh the alcohol amine, slowly drop into the mixed solution, and stir until p-nitrotoluene o-sulfonic acid Sulfonic acid dissolves completely.
[0018] 5) Raise the temperature of the mixture in step 1). After reaching the temperature, slowly add NaOH solution dropwise to the reaction solution. After keeping it warm for a period of time, add ethylene glycol monomethyl ether solution and stir evenly.
[0019] 6) Lower the temperature of the above 2) solution, after room temperature, use H 2 SO 4 The pH value of the solution was adjusted, filtered with suction, and dried to obtain a solid of Direct Yellow 11.
[0020] 1) Diethylene glycol ether, the molecular structure is CH 3 CH ...
Embodiment 1
[0022] Add 10ml of diethylene glycol ethyl ether to the three-neck flask, weigh 10g of p-nitrotoluene o-sulfonic acid with a content of 80-90%, add it to the water, stir evenly, raise the temperature to 60°C, add about 54ml of 10% NaOH solution , after stirring for 30min, add 10g of triethanolamine, after heat preservation for 8h, add Second Diol monomethyl ether 4ml, stir evenly, use H 2 SO 4 The solution was adjusted to pH 8, filtered with suction and dried.
Embodiment 2
[0024] Add 10ml of diethylene glycol ethyl ether to the three-neck flask, weigh 10g of p-nitrotoluene o-sulfonic acid with a content of 80-90%, add it to the water, stir evenly, raise the temperature to 60°C, add about 54ml of 10% NaOH solution , after stirring for 30min, add 3.4g of diethanolamine, heat preservation reaction for about 8h and finish heating, use H 2 SO 4 The solution was adjusted to pH 8, filtered with suction and dried.
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
Login to view more
Abstract
The invention discloses a method for improving direct yellow 11 dye-uptake, and relates to a method for improving dye-uptakes. 4-nitrotoluene-2-sulfonic acid as raw material and a NaOH solution undergo a self condensation reaction to produce direct yellow 11. The method comprises the following steps of weighing diethylene glycol monoethyl ether, putting it into a three-necked flask, weighing 4-nitrotoluene-2-sulfonic acid, putting it into the same three-necked flask, carrying out stirring well, weighing alcohol amine, slowly and dropwisely adding the alcohol amine into the mixed solution, stirring the mixed solution until the 4-nitrotoluene-2-sulfonic acid is completely dissolved, heating the mixed solution to a certain temperature, slowly and dropwisely adding a NaOH solution into the reaction solution, carrying out heat preservation for a period of time, adding an ethylene glycol monomethyl ether solution into the mixed solution, carrying out stirring well, then carrying out cooling, regulating the pH value by a H2SO4 solution, carrying out suction filtrating, and carrying out direct drying to obtain the direct yellow 11 solids. The direct yellow 11 prepared by the method has a high dye-uptake and is environmental friendly.
Description
Technical field [0001] The present invention involves a method of improving the upper dyeing rate, especially a method that involves an increase in direct yellow 11 upper dyeing rate. Background technique [0002] The direct dye is widely used for its simple synthesis process, convenient dyeing, and low price.In 1973, the output of direct dyes in my country reached 12,295 tons, which was the highest level in history.Direct dyes are very important in the printing and dyeing industry, especially knitting and silk industries.Under the current situation of various dyes, the sales of direct dyes are better.Direct yellow 11 dyes have been widely used in industry, printing, textiles and other industries.Its advantage is that the price is low, but its upper dyeing rate is low. Therefore, it is necessary to study the method of improving the direct dyeing rate of direct yellow 11. Invention content [0003] The purpose of the present invention is to provide a method to increase the dyeing...
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.