CN112175747A - Method for preparing textile detergent - Google Patents
Method for preparing textile detergent Download PDFInfo
- Publication number
- CN112175747A CN112175747A CN202011181969.5A CN202011181969A CN112175747A CN 112175747 A CN112175747 A CN 112175747A CN 202011181969 A CN202011181969 A CN 202011181969A CN 112175747 A CN112175747 A CN 112175747A
- Authority
- CN
- China
- Prior art keywords
- parts
- preparing
- textile detergent
- later use
- filler
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/046—Salts
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/14—Fillers; Abrasives ; Abrasive compositions; Suspending or absorbing agents not provided for in one single group of C11D3/12; Specific features concerning abrasives, e.g. granulometry or mixtures
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2065—Polyhydric alcohols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2086—Hydroxy carboxylic acids-salts thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2093—Esters; Carbonates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/382—Vegetable products, e.g. soya meal, wood flour, sawdust
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/384—Animal products
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38636—Preparations containing enzymes, e.g. protease or amylase containing enzymes other than protease, amylase, lipase, cellulase, oxidase or reductase
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- Zoology (AREA)
- Detergent Compositions (AREA)
Abstract
The invention discloses a method for preparing a textile detergent, which belongs to the technical field of preparation of softeners and comprises the following steps: (1) preparing an additive, (2) weighing raw materials, and (3) mixing to prepare a finished product. The method is simple, and the prepared detergent has the characteristics of strong oil and stain removal capacity and high efficiency.
Description
Technical Field
The invention belongs to the technical field of preparation of softening agents, and particularly relates to a preparation method of a textile detergent.
Background
Detergents are in a large category and are in a wide variety of forms, including both inorganic and organic dry cleaning. The organic detergents are simply detergents made of carbon-containing compounds, and the inorganic detergents are detergents made of carbon-free compounds, and thus they are inorganic. There are many methods for classifying detergents, and water-based detergents, semi-water-based detergents and non-water-based detergents are generally classified. The conventional textile detergents on the market mostly have the problems of common oil removal and dirt removal capability and poor comprehensive use effect, and need to be continuously improved.
Disclosure of Invention
The invention aims to provide a manufacturing method of a textile detergent.
The technical purpose of the invention is realized by the following technical scheme:
a method for manufacturing a textile detergent comprises the following steps:
(1) preparing an additive:
a. mixing and crushing sweet osmanthus, honeysuckle and lily to obtain a mixture A for later use;
b. b, putting the mixture A obtained in the operation a into boiling water, boiling for 1.5-2 h, and filtering to obtain a filtrate B for later use;
c. heating and concentrating the filtrate B obtained in the operation B to obtain an additive for later use;
(2) weighing raw materials:
weighing the following raw materials in parts by weight for later use: 10-15 parts of the additive prepared in the step (1), 6-9 parts of sodium citrate, 5-8 parts of potassium chloride, 18-22 parts of glycerol, 2-4 parts of complex enzyme, 4-8 parts of nonylphenol polyoxyethylene ether, 3-6 parts of gelatin, 12-16 parts of ethanolamine, 5-10 parts of methyl methacrylate, 4-7 parts of filler and 500-550 parts of deionized water;
(3) mixing to prepare a finished product:
a. heating deionized water, then adding the additive prepared in the step (1), sodium citrate, potassium chloride, glycerol, nonylphenol polyoxyethylene ether, gelatin, ethanolamine, methyl methacrylate and filler together, and performing ultrasonic dispersion uniformly for later use;
b. and d, after the solution obtained in the operation a is cooled to normal temperature, adding the complex enzyme, and uniformly stirring to obtain the finished product detergent.
Further, the weight ratio of the osmanthus fragrans, the honeysuckle and the lily in the step (1) in the operation a is 10-15: 3-6: 2-4.
Further, the corresponding weight ratio of the mixture A and boiling water in the step (1) and the operation b is 1: 6-7.
Further, after the heating concentration treatment in the operation c in the step (1), controlling the volume of the filtrate B to be concentrated to 12-16% of the original volume.
Further, the filler in the step (2) is any one of kaolin, attapulgite and diatomite.
Further, the particle size of the filler in the step (2) is 300-400 meshes.
Further, the complex enzyme in the step (2) is formed by mixing ficin and hesperidinase according to the weight ratio of 4-5: 1.
Further, the temperature of the deionized water is kept between 70 and 75 ℃ during the heating in the operation a in the step (3).
Further, the frequency of the ultrasonic wave is controlled to be 700-800 kHz during the ultrasonic dispersion in the operation a of the step (3).
Compared with the prior art, the invention has the following advantages:
the invention discloses a preparation method of a detergent, the detergent prepared by the method can obviously improve the washing and protecting effects on textiles, in the preparation process, an additive is prepared firstly, the additive is obtained by mixing and extracting sweet osmanthus, honeysuckle and lily together, the additive can endow the detergent with good antibacterial property, can assist other components to enhance the decontamination effect and can improve the integral smell; the added sodium citrate, potassium chloride, glycerol, nonylphenol polyoxyethylene ether, gelatin, ethanolamine and methyl methacrylate are compounded for use, so that the decontamination and deoiling capability is effectively ensured, and the fabric damage to the textile is small; the added filler can improve the stability of the effective components of the detergent, can adsorb and promote the removal of oil stains, and improves the using effect of the detergent. The detergent prepared by the method has the characteristics of strong oil and stain removal capacity and high efficiency, and has great market competitiveness.
Detailed Description
Example 1
A method for manufacturing a textile detergent comprises the following steps:
(1) preparing an additive:
a. mixing and crushing sweet osmanthus, honeysuckle and lily to obtain a mixture A for later use;
b. b, putting the mixture A obtained in the operation a into boiling water, boiling for 1.5 hours, and filtering to obtain filtrate B for later use;
c. heating and concentrating the filtrate B obtained in the operation B to obtain an additive for later use;
(2) weighing raw materials:
weighing the following raw materials in parts by weight for later use: 10 parts of the additive prepared in the step (1), 6 parts of sodium citrate, 5 parts of potassium chloride, 18 parts of glycerol, 2 parts of complex enzyme, 4 parts of nonylphenol polyoxyethylene ether, 3 parts of gelatin, 12 parts of ethanolamine, 5 parts of methyl methacrylate, 4 parts of filler and 500 parts of deionized water;
(3) mixing to prepare a finished product:
a. heating deionized water, then adding the additive prepared in the step (1), sodium citrate, potassium chloride, glycerol, nonylphenol polyoxyethylene ether, gelatin, ethanolamine, methyl methacrylate and filler together, and performing ultrasonic dispersion uniformly for later use;
b. and d, after the solution obtained in the operation a is cooled to normal temperature, adding the complex enzyme, and uniformly stirring to obtain the finished product detergent.
And (2) in the step (1), when the sweet osmanthus, the honeysuckle and the lily are mixed together, the corresponding weight ratio is 10:3: 2.
The corresponding weight ratio of the mixture A and the boiling water in the operation b in the step (1) is 1:6.
Controlling the volume of the filtrate B to be concentrated to 12% after the heating concentration treatment in the operation c of the step (1).
The filler in the step (2) is kaolin.
The particle size of the filler in the step (2) is 300 meshes.
The complex enzyme in the step (2) is formed by mixing ficin and hesperidinase according to the weight ratio of 4: 1.
The deionized water was maintained at a temperature of 70 ℃ during the heating described in operation a of step (3).
Controlling the frequency of the ultrasonic wave to be 700kHz during the ultrasonic dispersion in the operation a of the step (3).
Example 2
A method for manufacturing a textile detergent comprises the following steps:
(1) preparing an additive:
a. mixing and crushing sweet osmanthus, honeysuckle and lily to obtain a mixture A for later use;
b. b, putting the mixture A obtained in the operation a into boiling water, boiling for 1.8 hours, and filtering to obtain filtrate B for later use;
c. heating and concentrating the filtrate B obtained in the operation B to obtain an additive for later use;
(2) weighing raw materials:
weighing the following raw materials in parts by weight for later use: 13 parts of the additive prepared in the step (1), 8 parts of sodium citrate, 7 parts of potassium chloride, 20 parts of glycerol, 3 parts of complex enzyme, 6 parts of nonylphenol polyoxyethylene ether, 5 parts of gelatin, 15 parts of ethanolamine, 8 parts of methyl methacrylate, 6 parts of filler and 530 parts of deionized water;
(3) mixing to prepare a finished product:
a. heating deionized water, then adding the additive prepared in the step (1), sodium citrate, potassium chloride, glycerol, nonylphenol polyoxyethylene ether, gelatin, ethanolamine, methyl methacrylate and filler together, and performing ultrasonic dispersion uniformly for later use;
b. and d, after the solution obtained in the operation a is cooled to normal temperature, adding the complex enzyme, and uniformly stirring to obtain the finished product detergent.
And (2) in the step (1), when the sweet osmanthus, the honeysuckle and the lily are mixed together, the corresponding weight ratio is 14:5: 3.
The corresponding weight ratio of the mixture A to the boiling water in the operation b in the step (1) is 1: 6.6.
Controlling the volume of the filtrate B to be concentrated to 15% after the heating concentration treatment in the operation c of the step (1).
The filler in the step (2) is attapulgite.
The particle size of the filler in the step (2) is 350 meshes.
The complex enzyme in the step (2) is formed by mixing ficin and hesperidinase according to the weight ratio of 4.5: 1.
The deionized water was maintained at a temperature of 72 ℃ during the heating described in operation a of step (3).
Controlling the frequency of the ultrasonic wave to be 780kHz during the ultrasonic dispersion in the operation a of the step (3).
Example 3
A method for manufacturing a textile detergent comprises the following steps:
(1) preparing an additive:
a. mixing and crushing sweet osmanthus, honeysuckle and lily to obtain a mixture A for later use;
b. b, putting the mixture A obtained in the operation a into boiling water, boiling for 2 hours, and filtering to obtain filtrate B for later use;
c. heating and concentrating the filtrate B obtained in the operation B to obtain an additive for later use;
(2) weighing raw materials:
weighing the following raw materials in parts by weight for later use: 15 parts of the additive prepared in the step (1), 9 parts of sodium citrate, 8 parts of potassium chloride, 22 parts of glycerol, 4 parts of complex enzyme, 8 parts of nonylphenol polyoxyethylene ether, 6 parts of gelatin, 16 parts of ethanolamine, 10 parts of methyl methacrylate, 7 parts of filler and 550 parts of deionized water;
(3) mixing to prepare a finished product:
a. heating deionized water, then adding the additive prepared in the step (1), sodium citrate, potassium chloride, glycerol, nonylphenol polyoxyethylene ether, gelatin, ethanolamine, methyl methacrylate and filler together, and performing ultrasonic dispersion uniformly for later use;
b. and d, after the solution obtained in the operation a is cooled to normal temperature, adding the complex enzyme, and uniformly stirring to obtain the finished product detergent.
And (2) in the step (1), when the sweet osmanthus, the honeysuckle and the lily are mixed together, the corresponding weight ratio is 15:6: 4.
The corresponding weight ratio of the mixture A and the boiling water in the operation b in the step (1) is 1: 7.
Controlling the volume of the filtrate B to be concentrated to 16% after the heating concentration treatment in the operation c of the step (1).
The filler in the step (2) is diatomite.
The particle size of the filler in the step (2) is 400 meshes.
The complex enzyme in the step (2) is formed by mixing ficin and hesperidinase according to the weight ratio of 5: 1.
The deionized water was maintained at a temperature of 75 ℃ during the heating described in operation a of step (3).
Controlling the frequency of the ultrasonic waves to be 800kHz during the ultrasonic dispersion in the operation a of the step (3).
Comparative example 1
This comparative example 1 is compared to example 2 only with the difference that the additive preparation treatment of step (1) is omitted except that the process steps are otherwise identical.
Comparative example 2
This comparative example 2 is different from example 2 only in that the filler component in the raw material weighing in step (2) is omitted, and the steps are the same except for the other steps.
In order to compare the effects of the invention, the detergents prepared in the above example 2 and comparative examples 1-2 were tested, specifically: 5.00g of detergent is correspondingly taken from each group and dispersed in 2500mL of hard water, after the detergent is evenly shaken, 800mL of test solution is respectively measured in three washing barrels of a vertical decontamination machine, when the temperature of the test solution rises to 30 ℃, the cotton cloth (with the mass of m1) with oil stain of known weight and a washing rack are correspondingly put into the washing barrels, the soaking time starts to be counted after the last washing rack is put into the washing barrels, meanwhile, a stirrer is quickly arranged, the decontamination machine is started to start washing after being soaked for 1min, the machine is automatically stopped when 3min, the stirrer is quickly taken down, the washing rack is taken out, the washed cotton cloth with oil stain is clamped on the original airing rack one by one, and the cotton cloth with oil stain is arranged on the corresponding weighing rack and weighed to be m2 after being hung and aired for 3 h. The deoiling rate omega is (m1-m2)/m 1; the specific contrast data for each set are shown in table 1 below:
TABLE 1
| Oil removal rate omega (%) | |
| Example 2 | 33.7 |
| Comparative example 1 | 24.5 |
| Comparative example 2 | 18.1 |
As can be seen from the above table 1, the detergent prepared by the method of the invention has good cleaning and oil removing effects, and has the characteristics of good taste, safe use performance and environmental protection when in use.
Claims (9)
1. The manufacturing method of the textile detergent is characterized by comprising the following steps:
(1) preparing an additive:
a. mixing and crushing sweet osmanthus, honeysuckle and lily to obtain a mixture A for later use;
b. b, putting the mixture A obtained in the operation a into boiling water, boiling for 1.5-2 h, and filtering to obtain a filtrate B for later use;
c. heating and concentrating the filtrate B obtained in the operation B to obtain an additive for later use;
(2) weighing raw materials:
weighing the following raw materials in parts by weight for later use: 10-15 parts of the additive prepared in the step (1), 6-9 parts of sodium citrate, 5-8 parts of potassium chloride, 18-22 parts of glycerol, 2-4 parts of complex enzyme, 4-8 parts of nonylphenol polyoxyethylene ether, 3-6 parts of gelatin, 12-16 parts of ethanolamine, 5-10 parts of methyl methacrylate, 4-7 parts of filler and 500-550 parts of deionized water;
(3) mixing to prepare a finished product:
a. heating deionized water, then adding the additive prepared in the step (1), sodium citrate, potassium chloride, glycerol, nonylphenol polyoxyethylene ether, gelatin, ethanolamine, methyl methacrylate and filler together, and performing ultrasonic dispersion uniformly for later use;
b. and d, after the solution obtained in the operation a is cooled to normal temperature, adding the complex enzyme, and uniformly stirring to obtain the finished product detergent.
2. The manufacturing method of the textile detergent according to claim 1, wherein the weight ratio of the osmanthus fragrans, the honeysuckle and the lily in the operation a in the step (1) is 10-15: 3-6: 2-4.
3. The method for manufacturing the textile detergent according to claim 1, wherein the corresponding weight ratio of the mixed material A and the boiling water in the step (1) and the operation b is 1: 6-7.
4. The method for preparing a textile detergent as claimed in claim 1, wherein the volume of the filtrate B is controlled to be concentrated to 12-16% of the original volume after the heating concentration treatment in the operation c of the step (1).
5. The method for preparing a textile detergent according to claim 1, wherein the filler in the step (2) is any one of kaolin, attapulgite and diatomite.
6. The method for preparing a textile detergent as claimed in claim 1, wherein the particle size of the filler in step (2) is 300-400 mesh.
7. The method for preparing the textile detergent as claimed in claim 1, wherein the complex enzyme in the step (2) is prepared by mixing ficin and hesperidinase according to a weight ratio of 4-5: 1.
8. The method for preparing a textile detergent as claimed in claim 1, wherein the temperature of the deionized water is maintained at 70-75 ℃ during the heating in operation a of step (3).
9. The method for preparing a textile detergent according to claim 1, wherein the frequency of the ultrasonic waves is controlled to be 700 to 800kHz during the ultrasonic dispersion in the operation a of the step (3).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202011181969.5A CN112175747A (en) | 2020-10-29 | 2020-10-29 | Method for preparing textile detergent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202011181969.5A CN112175747A (en) | 2020-10-29 | 2020-10-29 | Method for preparing textile detergent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN112175747A true CN112175747A (en) | 2021-01-05 |
Family
ID=73917756
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202011181969.5A Pending CN112175747A (en) | 2020-10-29 | 2020-10-29 | Method for preparing textile detergent |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN112175747A (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107012027A (en) * | 2017-04-28 | 2017-08-04 | 袁晓霞 | A kind of bedding detergent |
| CN108102805A (en) * | 2017-12-05 | 2018-06-01 | 徐云丽 | Detergent composition |
| CN110964607A (en) * | 2019-11-01 | 2020-04-07 | 付世宁 | Laundry detergent with sterilization function and preparation method thereof |
-
2020
- 2020-10-29 CN CN202011181969.5A patent/CN112175747A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107012027A (en) * | 2017-04-28 | 2017-08-04 | 袁晓霞 | A kind of bedding detergent |
| CN108102805A (en) * | 2017-12-05 | 2018-06-01 | 徐云丽 | Detergent composition |
| CN110964607A (en) * | 2019-11-01 | 2020-04-07 | 付世宁 | Laundry detergent with sterilization function and preparation method thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69124425T2 (en) | Process and composition for treating textiles | |
| DE69123869T2 (en) | Alkanol ammonium-functional siloxanes containing plasticizer composition | |
| DE69117207T2 (en) | Quaternary ammonium-functional siloxanes containing plasticizer compositions | |
| DE2215371A1 (en) | laundry detergent | |
| EP0743358B1 (en) | Composition for washing and cleaning of textile materials | |
| US9090997B2 (en) | Fabrication of natural cellulose fiber with flame-retarding capability | |
| DE2628879A1 (en) | METHOD AND DEVICE FOR WASHING TEXTILES | |
| CN110106037B (en) | Anti-cross-color detergent | |
| EP0017120B2 (en) | Textile detergent acting as a finishing agent | |
| CN108504472B (en) | Environment-friendly washing powder | |
| EP0002951B1 (en) | Textile materials having durable soil release and moisture transport characteristics and process for producing same | |
| CN110735316A (en) | antibacterial knitted fabric and production method thereof | |
| CN115216961A (en) | Bio-based multi-in-one textile scouring agent and preparation method and application thereof | |
| CN112175747A (en) | Method for preparing textile detergent | |
| EP2427539B1 (en) | Bluing composition and method for treating textile articles using the same | |
| CN106637979A (en) | Anti-bacterial anti-mite towel regenerated cotton yarn textile material and preparation method thereof | |
| CN109183160A (en) | A kind of natural feather washing process | |
| JP2007535626A (en) | Fabric useful composition | |
| JPS6116999A (en) | Photoactivation-bleaching detergent composition and use | |
| US3994682A (en) | Two-step washing method for textiles | |
| CN105039003B (en) | A kind of fabric washing and waste water circulation reuse detergent and its production and use | |
| DE2226934A1 (en) | QUATERNAERE AMMONIUM COMPOUNDS AND THEIR USE FOR SURFACE TREATMENT | |
| CN108867018B (en) | Washing-free washing process for clothes | |
| KR100432586B1 (en) | Composition for laundry and method for producing the same | |
| KR101732366B1 (en) | Tissue for laundry using recycled waste polyvinylalcohol and method for preparing the same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20210105 |