CN108179073B - Mild bactericidal laundry detergent and preparation method thereof - Google Patents

Mild bactericidal laundry detergent and preparation method thereof Download PDF

Info

Publication number
CN108179073B
CN108179073B CN201810030166.6A CN201810030166A CN108179073B CN 108179073 B CN108179073 B CN 108179073B CN 201810030166 A CN201810030166 A CN 201810030166A CN 108179073 B CN108179073 B CN 108179073B
Authority
CN
China
Prior art keywords
parts
rotating speed
adjusting
alkyl glycoside
laundry detergent
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.)
Expired - Fee Related
Application number
CN201810030166.6A
Other languages
Chinese (zh)
Other versions
CN108179073A (en
Inventor
张潇瀚
张建军
马丹珂
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201810030166.6A priority Critical patent/CN108179073B/en
Publication of CN108179073A publication Critical patent/CN108179073A/en
Application granted granted Critical
Publication of CN108179073B publication Critical patent/CN108179073B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/835Mixtures of non-ionic with cationic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H1/00Processes for the preparation of sugar derivatives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/02Acyclic radicals, not substituted by cyclic structures
    • C07H15/04Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/22Carbohydrates or derivatives thereof
    • C11D3/222Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/382Vegetable products, e.g. soya meal, wood flour, sawdust
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/48Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/662Carbohydrates or derivatives
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/667Neutral esters, e.g. sorbitan esters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Emergency Medicine (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

The invention provides a mild sterilization laundry detergent which comprises the following components in parts by mass based on 100 parts by mass: 1.0-3.0 parts of alkyl glycoside citrate, 3.0-10.0 parts of alkyl glycoside, 1.5-2.5 parts of glycosyl amide quaternary ammonium salt, 1.5-3.0 parts of artemisinin extracting solution, 0.1-1 part of thickening agent, 0.1-5 parts of other auxiliary agents and the balance of deionized water. The laundry detergent has the advantages of mild sterilization, no residue and easy degradation, is suitable for washing infant clothes and close-fitting clothes, and has wide application prospect. Meanwhile, the invention also provides a preparation method of the mild sterilization laundry detergent.

Description

Mild bactericidal laundry detergent and preparation method thereof
Technical Field
The invention belongs to the field of washing products, and particularly relates to a mild bactericidal laundry detergent and a preparation method thereof.
Background
Compared with washing powder, the laundry detergent has the advantages of easy dissolution, high active matter content, convenient use and the like, and is very popular with people. However, most of the conventional laundry detergent formulations use sulfate, alcohol ether carboxylate or sulfonate surfactants as active substances, alkanolamide 6501 as a thickening agent, alcohol ether and alcohol ether glycoside substances as main components, dioxane easily remains, and C is8-16The quaternary ammonium salt cationic surfactant is used as a bactericide, so that the laundry detergent has strong irritation, harmful substances are easy to remain on washed articles, the laundry detergent is used for washing clothes, especially infant clothes and underwear, the body health of people can be affected, and meanwhile, the formula contains a part of difficultly-degradable components and can pollute the environment. Therefore, the development of a laundry detergent which has biocompatibility, has a killing effect on pathogenic microorganisms, has no harmful substance residue, and is mild and moist to skin can meet new requirements of people on clothes health and environmental protection.
The glucoside citrate surfactant has good stability, can chelate metal ions to improve the hard water resistance of a formula, has excellent low-temperature solubility and easy rinsing performance, can be compounded with various surfactants and assistants, cannot form an insoluble organic complex particularly when being compounded with a cationic surfactant or other cationic assistants, and is a green multifunctional surfactant. Although alkyl glycoside citrate belongs to alkyl glycoside citrate surfactants, the main production raw materials of fatty alcohol, glucose, citric acid and the like are biomass-based renewable raw materials derived from natural products, are safe, non-toxic and easy to degrade, the product is not localized at present due to the limitation of the production technology of the alkyl glycoside citrate, and the application cost is greatly improved mainly by depending on the over-high price of the imported product. Therefore, the method for synthesizing the alkyl glycoside citrate which is low in cost and easy to dissolve in the laundry detergent is developed, and has important practical significance for developing the bactericidal laundry detergent with mild research performance.
Disclosure of Invention
In view of the above, the invention provides a mild bactericidal laundry detergent and a preparation method thereof, so as to solve the above problems.
Specifically, the invention adopts the following technical scheme:
the mild sterilization laundry detergent comprises the following components in parts by mass based on 100 parts by mass: 1.0-3.0 parts of alkyl glycoside citrate, 3.0-10.0 parts of alkyl glycoside, 1.5-2.5 parts of glycosyl amide quaternary ammonium salt, 1.5-3.0 parts of artemisinin extracting solution, 0.1-1 part of thickening agent, 0.1-5 parts of other auxiliary agents and the balance of deionized water.
Preferably, the alkyl glycoside citrate is a compound having the general formula:
Figure BDA0001546251920000021
wherein R is an alkyl group having a carbon chain length of 8 to 14 carbons, and n is 1.2 to 1.6.
Preferably, the quaternary ammonium glycosylamide salt is a compound having the general formula:
Figure BDA0001546251920000022
wherein R is1Is glucosyl or lactose group; r2Is an alkyl group having a carbon chain length of 10 to 16 carbons.
Based on the above, it comprises the following components in parts by mass, calculated as 100 parts by mass: 1.8-2.5 parts of alkyl glycoside citrate, 7.0-7.5 parts of alkyl glycoside, 1.5-2.5 parts of glycosyl amide quaternary ammonium salt, 2.0-2.5 parts of artemisinin extracting solution, 0.5-4 parts of thickening agent, 0.5-0.7 part of other auxiliary agents and the balance of deionized water.
Based on the above, the artemisinin extracting solution is obtained by steaming, extracting and concentrating dry artemisia apiacea leaves by deionized water, and the concentration of artemisinin in the artemisinin extracting solution is 1.5-2.5 g/ml.
Based on the above, the thickener is sodium alginate, xanthan gum or pectin.
Based on the above, the other auxiliary agents are one or a mixture of at least two of essence, fluorescent whitening agent, sodium hydroxide, potassium hydroxide and pigment.
Based on the above, the pH value of the mild sterilization laundry detergent is 7.0-7.5.
The preparation method of the mild bactericidal laundry detergent comprises the following steps: firstly, reacting citric acid and alkyl glucoside in a reaction kettle with a stirring head and an emulsifying head in the kettle under the vacuum condition under the catalysis of a hydrogen peroxide composite catalyst to obtain a mixed solution of alkyl glucoside citrate and alkyl glucoside; adding glycosyl amide quaternary ammonium salt, artemisinin extracting solution, thickening agent, other auxiliary agents and deionized water into the mixed solution, and uniformly mixing to obtain a laundry detergent product; the hydrogen peroxide composite catalyst comprises ethylene diamine tetraacetic acid and hydrogen peroxide, and the mass ratio of the ethylene diamine tetraacetic acid to the hydrogen peroxide is (96-99): (1-4).
Based on the above, the step of obtaining the mixed solution comprises: firstly adjusting the rotating speed of the stirring head to be 20-60 r/min, adjusting the rotating speed of the emulsifying head to be 30-800 r/min, adding 27-38% of alkyl glycoside aqueous solution by mass fraction into the reaction kettle, then gradually adding citric acid, increasing the rotating speed of the emulsifying head according to the acceleration of 100-200 r/min increase per minute in the process of adding the citric acid, after finishing adding the citric acid for 20-50 min, adjusting the rotating speed of the stirring head to be 80-120 r/min, adjusting the rotating speed of the emulsifying head to be 13000-15000 r/min, adding the hydrogen peroxide composite catalyst, and reacting for 30-60 min under the conditions of vacuum degree of 4000-8000 Pa and temperature of 36-48 ℃ to obtain the mixed solution.
Based on the above, the steps of obtaining the laundry detergent product comprise: firstly adjusting the rotating speed of the emulsifying head to 800-1000 r/min, adjusting the rotating speed of the stirring head to 30-60 r/min, adding the glycosyl amide quaternary ammonium salt and the artemisinin extracting solution and supplementing deionized water to 90% of the formula amount, then adding the thickening agent and stirring for 30-60 min to mix uniformly, then adjusting the pH value to 7.0-7.5, removing the vacuum in the reaction kettle and adjusting the vacuum to normal pressure, then adding the other auxiliary agents and the rest deionized water, adjusting the rotating speed of the emulsifying head to 300-500 r/min, adjusting the rotating speed of the stirring head to 20-50 r/min, and continuing stirring for 30-50 min to obtain the laundry detergent product.
Based on the above, in the step of obtaining the mixed solution, the mass ratio of the hydrogen peroxide composite catalyst to the alkyl glycoside added is (1.5-10): 100.
compared with the prior art, the invention has outstanding substantive characteristics and remarkable progress. Specifically, the mild sterilization laundry detergent provided by the invention takes alkyl glucoside citrate and alkyl glucoside as main active ingredients, and the compounding of the alkyl glucoside citrate and the alkyl glucoside is warmer for human skin, has a good effect of moistening skin, is more suitable for hand washing, and is not only suitable for washing infants and underwear; meanwhile, the glycosyl amide quaternary ammonium salt which has the glycosyl and the quaternary ammonium salt with high surface activity and high efficiency and strong bactericidal property is compounded with the artemisinin extracting solution to be used as the bactericide, so that the bactericidal effect can be ensured, and the generation of drug resistance can be avoided; furthermore, the thickening agent of the mild bactericidal laundry detergent is low in irritation due to the adoption of natural thickening agents such as sodium alginate, xanthan gum or pectin, no harmful substances are generated in the production or use process, and the mild bactericidal laundry detergent is more environment-friendly; furthermore, the mild sterilization laundry detergent is neutral, is milder, and is suitable for washing infant clothes and close-fitting clothes.
Meanwhile, the preparation method of the mild sterilization laundry detergent provided by the invention is simple, easy to operate and suitable for large-scale production; meanwhile, the method also comprises a step of preparing alkyl glycoside citrate, wherein the alkyl glycoside citrate is prepared by reacting alkyl glycoside and citric acid under the catalysis of a hydrogen peroxide composite catalyst, and the alkyl glycoside is excessive, so that a product after the reaction is mainly a mixed solution of the alkyl glycoside citrate and the alkyl glycoside, can be directly used, and the cost of the mild sterilization laundry detergent is effectively reduced; meanwhile, ethylene diamine tetraacetic acid in the hydrogen peroxide composite catalyst can play a role of a stabilizer, so that hydrogen peroxide is prevented from losing catalytic action by being reduced in the reaction process of alkyl glycoside and citric acid, inorganic base is added after the reaction of alkyl glycoside and citric acid is finished to adjust the pH value to be alkalescence, the ethylene diamine tetraacetic acid is neutralized and cannot play a role of the stabilizer any more, the hydrogen peroxide is reduced to water, no residue is generated, and irritation to infant clothes is avoided.
Detailed Description
The technical solution of the present invention is further described in detail by the following embodiments.
Example 1
The mild bactericidal laundry detergent comprises the following components in percentage by weight:
Figure BDA0001546251920000051
wherein, 1ml of the artemisinin extract contains 1.5g of artemisinin.
The mild sterilization laundry detergent is prepared in a reaction kettle with a stirring head and an emulsifying head inside, and the preparation method comprises the following steps:
preparation of alkyl glycoside citrate C8-10Mixing alkyl glycoside and partial deionized water to obtain C with mass fraction of 30%8-10An aqueous solution of an alkylglycoside, adding said C8-10Adding an alkyl glycoside aqueous solution into the reaction kettle, adjusting the rotating speed of the stirring head to be 50r/min, adjusting the rotating speed of the emulsifying head to be 600r/min, stirring for 15min, gradually adding citric acid, simultaneously increasing the rotating speed of the emulsifier to be 200r/min per minute, controlling the adding time of the citric acid to be 30min, adjusting the rotating speed of the emulsifying head to be 13000r/min after the addition of the citric acid is finished, adjusting the rotating speed of the stirring head to be 80r/min, adding a hydrogen peroxide composite catalyst, reacting for 40min under the conditions that the vacuum degree is 5000Pa and the reaction temperature is 42 ℃ to obtain a mixed solution of alkyl glycoside citrate and alkyl glycoside, sampling and detecting the content of the citric acid in the mixed solution to be 0.05%, and the hydrogen peroxide composite catalyst and the C are mixed catalyst8-10The mass ratio of the alkyl glycoside is 1: 10; the mass ratio of ethylene diamine tetraacetic acid to hydrogen peroxide in the hydrogen peroxide composite catalyst is 96: 4;
adjusting the rotating speed of the emulsifying head to 800r/min, the rotating speed of the stirring head to 50r/min, and keeping the vacuum degree to 5000Pa in the product preparation, and adding C into the reaction kettle14Adding 90% deionized water into glycosyl amide quaternary ammonium salt and artemisinin extracting solution, adding sodium alginate, and stirring for 50 min; and dropwise adding sodium hydroxide into the reaction kettle, adjusting the pH value of the solution to be 7.0, removing the vacuum, adjusting the solution to be normal pressure, adding essence, indigo and the rest deionized water into the reaction kettle, adjusting the rotating speed of the emulsifying head to be 500r/min, adjusting the rotating speed of the stirring head to be 30r/min, and continuously stirring for 30min until the solution is uniform and transparent to obtain the mild sterilization laundry detergent product.
Example 2
The mild bactericidal laundry detergent comprises the following components in percentage by weight:
Figure BDA0001546251920000061
wherein, each 1ml of the artemisinin extract contains 2.5g of artemisinin.
The mild sterilization laundry detergent is prepared in a reaction kettle with a stirring head and an emulsifying head inside, and the preparation method comprises the following steps:
preparation of alkyl glycoside citrate C10-12Mixing alkyl glycoside and partial deionized water to obtain C with mass fraction of 27%10-12An aqueous solution of an alkylglycoside, adding said C10-12Adding an alkyl glycoside aqueous solution into the reaction kettle, adjusting the rotating speed of the stirring head to be 60r/min, adjusting the rotating speed of the emulsifying head to be 800r/min, stirring for 20min, gradually adding citric acid, simultaneously increasing the rotating speed of the emulsifying head by 150r/min per minute, controlling the adding time of the citric acid to be 50min, adjusting the rotating speed of the emulsifying head to be 14000r/min after the citric acid is added, adjusting the rotating speed of the stirring head to be 80r/min, adding a hydrogen peroxide composite catalyst, reacting for 45min under the conditions that the vacuum degree is 4500Pa and the reaction temperature is 45 ℃ to obtain a mixed solution of alkyl glycoside citrate and alkyl glycoside, sampling and detecting the content of the citric acid in the mixed solution to be 0.07%, and adjusting the rotating speed of the hydrogen peroxide composite catalyst and the C to be 60r/min10-12The mass ratio of the alkyl glycoside is 7.2: 100; the hydrogen peroxide composite catalyst consists of ethylene diamine tetraacetic acid and hydrogen peroxide, and the mass ratio of the ethylene diamine tetraacetic acid to the hydrogen peroxide is 97: 3;
adjusting the rotating speed of the emulsifying head to 600r/min, the rotating speed of the stirring head to 60r/min, maintaining the vacuum degree to 4500Pa, and adding C into the reaction kettle16Adding 90% deionized water into glycosyl amide quaternary ammonium salt and artemisinin extracting solution, adding sodium alginate, and continuously stirring for 50 min; and dropwise adding sodium hydroxide into the reaction kettle, adjusting the pH value to 7.2, removing the vacuum, adjusting the pressure to normal pressure, continuously adding essence, indigo violet and the rest deionized water into the reaction kettle, adjusting the rotating speed of the emulsifying head to 600r/min, continuously stirring the mixture for 30min until the solution is uniform and transparent, and thus obtaining the mild sterilization laundry detergent product.
Example 3
The laundry detergent comprises the following components in percentage by weight:
Figure BDA0001546251920000071
wherein, each 1ml of the artemisinin extract contains 2.0g of artemisinin.
The mild sterilization laundry detergent is prepared in a reaction kettle with a stirring head and an emulsifying head inside, and the preparation method comprises the following steps:
preparation of alkyl glycoside citrate C12-14Mixing alkyl glycoside and partial deionized water to obtain 38% C8-10An aqueous solution of an alkylglycoside, adding said C12-14Adding alkyl glycoside aqueous solution into in the reation kettle, adjusting the rotational speed of agitator head is 20r/min, the rotational speed of emulsification head 700r/min, stirring 40min, add citric acid gradually, increase every minute simultaneously at the in-process of adding citric acid emulsification head rotational speed 180r/min, the control of the time of addition of citric acid is at 60min, adjust after citric acid adds, the rotational speed of emulsification head 15000r/min, the rotational speed of agitator head is 100r/min, adds hydrogen peroxide composite catalyst, under the condition that vacuum is 4200Pa, reaction temperature is 42 ℃, reaction 60min obtains the mixed solution of alkyl glycoside citrate and alkyl glycoside, the sample detection citric acid content in the mixed solution is 0.05%, hydrogen peroxide composite catalyst with C12-14The mass ratio of the alkyl glycoside is 1.5: 100; the hydrogen peroxide composite catalyst consists of ethylene diamine tetraacetic acid and hydrogen peroxide, and the mass ratio of the ethylene diamine tetraacetic acid to the hydrogen peroxide is 99: 1;
adjusting the rotation speed of the emulsifying head to be 500r/min, the rotation speed of the stirring head to be 60r/min, keeping the vacuum degree to be 4200Pa, and adding C into the reaction kettle12Adding 90% deionized water into glycosyl amide quaternary ammonium salt and artemisinin extracting solution, adding sodium alginate, and continuously stirring for 50 min; and (3) dropwise adding potassium hydroxide into the reaction kettle, adjusting the pH value to 7.5, removing the vacuum, adjusting the pressure to normal pressure, continuously adding essence, indigo and the rest deionized water, adjusting the rotating speed of the emulsifying head to 500r/min, adjusting the rotating speed of the stirring head to 50r/min, and continuously stirring for 50min until the solution is uniform and transparent, thereby obtaining the mild sterilization laundry detergent product.
Performance testing
The mild sterilization laundry detergent obtained in the examples 1 to 3 has no peculiar smell, and no suspended matters or precipitates. The detection proves that the stability of the laundry detergent is good, the laundry detergent is placed in a refrigerator at the temperature of (5 +/-2) ℃ for 24 hours, and the laundry detergent is observed when taken out and restored to the room temperature, is not layered, has no precipitate, and is transparent and not turbid; placing in a heat preservation box at the temperature of (40 +/-2) ℃ for 24h, taking out and observing, wherein the product is not layered, has no precipitate, and is transparent and not turbid.
Through detection, all indexes of the mild sterilization laundry detergent provided by the invention meet the standard requirements of GB/T1224-2007 liquid detergent for clothing.
Finally, it should be noted that: the above examples are only intended to illustrate the technical solution of the present invention and not to limit it; although the present invention has been described in detail with reference to preferred embodiments, those skilled in the art will understand that: modifications to the specific embodiments of the invention or equivalent substitutions for parts of the technical features may be made; without departing from the spirit of the present invention, it is intended to cover all aspects of the invention as defined by the appended claims.

Claims (1)

1. A preparation method of a mild bactericidal laundry detergent comprises the following steps:
in a reaction kettle internally provided with a stirring head and an emulsifying head, under the vacuum condition, firstly adjusting the rotating speed of the stirring head to be 20-60 r/min, the rotating speed of the emulsifying head is 30-800 r/min, alkyl glycoside aqueous solution with the mass fraction of 27% -38% is added into the reaction kettle, then citric acid is gradually added, in the process of adding the citric acid, the rotating speed of the emulsifying head is increased according to the acceleration of 100-200 r/min per minute, after the citric acid is added for 20-50 min, the rotating speed of the stirring head is adjusted to 80-120 r/min, the rotating speed of the emulsifying head is 13000-15000 r/min, then the hydrogen peroxide composite catalyst is added, reacting for 30-60 min under the conditions that the vacuum degree is 4000-8000 Pa and the temperature is 36-48 ℃ to obtain a mixed solution of alkyl glycoside citrate and alkyl glycoside; wherein the mass ratio of the added hydrogen peroxide composite catalyst to the alkyl glycoside is (1.5-10): 100, respectively; the hydrogen peroxide composite catalyst comprises ethylene diamine tetraacetic acid and hydrogen peroxide, and the mass ratio of the ethylene diamine tetraacetic acid to the hydrogen peroxide is (96-99): (1-4);
adjusting the rotating speed of the emulsifying head to be 800-1000 r/min again, adjusting the rotating speed of the stirring head to be 30-60 r/min, adding glycosyl amide quaternary ammonium salt and artemisinin extracting solution into the mixed solution, supplementing deionized water to 90% of the formula amount, adding a thickening agent, stirring for 30-60 min, uniformly mixing, adjusting the pH value to be 7.0-7.5, removing the vacuum in the reaction kettle, adjusting the vacuum to be normal pressure, adding other auxiliary agents and the rest deionized water, adjusting the rotating speed of the emulsifying head to be 300-500 r/min, adjusting the rotating speed of the stirring head to be 20-50 r/min, and continuously stirring for 30-50 min to obtain the mild sterilization laundry detergent;
wherein the thickening agent is sodium alginate, xanthan gum or pectin; the other auxiliary agents are one or the mixture of at least two of essence, fluorescent whitening agent, sodium hydroxide, potassium hydroxide and pigment;
the mild sterilization laundry detergent comprises the following components in parts by mass based on 100 parts by mass: 1.0-3.0 parts of alkyl glycoside citrate, 3.0-10.0 parts of alkyl glycoside, 1.5-2.5 parts of glycosyl amide quaternary ammonium salt, 1.5-3.0 parts of artemisinin extracting solution, 0.1-1 part of thickening agent, 0.1-5 parts of other auxiliary agents and the balance of deionized water.
CN201810030166.6A 2018-01-12 2018-01-12 Mild bactericidal laundry detergent and preparation method thereof Expired - Fee Related CN108179073B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810030166.6A CN108179073B (en) 2018-01-12 2018-01-12 Mild bactericidal laundry detergent and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810030166.6A CN108179073B (en) 2018-01-12 2018-01-12 Mild bactericidal laundry detergent and preparation method thereof

Publications (2)

Publication Number Publication Date
CN108179073A CN108179073A (en) 2018-06-19
CN108179073B true CN108179073B (en) 2020-05-15

Family

ID=62550399

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810030166.6A Expired - Fee Related CN108179073B (en) 2018-01-12 2018-01-12 Mild bactericidal laundry detergent and preparation method thereof

Country Status (1)

Country Link
CN (1) CN108179073B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110870483A (en) * 2018-08-30 2020-03-10 洛阳蓝新生物科技有限公司 Artemisinin silver ion composite disinfectant
CN112280623B (en) * 2020-11-12 2022-01-04 福建省佑达环保材料有限公司 Water-based neutral cleaning solution for semiconductor manufacturing base station

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103555450A (en) * 2013-11-05 2014-02-05 中国日用化学工业研究院 Antibacterial decontaminating liquid detergent and preparation method thereof
CN103805367A (en) * 2014-02-28 2014-05-21 刘菊 High-efficiency sterilization laundry detergent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103555450A (en) * 2013-11-05 2014-02-05 中国日用化学工业研究院 Antibacterial decontaminating liquid detergent and preparation method thereof
CN103805367A (en) * 2014-02-28 2014-05-21 刘菊 High-efficiency sterilization laundry detergent

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
烷基糖苷及其衍生物的技术进展;杨秀全等;《日用化学工业》;20120630;第42卷(第3期);第215页右栏2.3.1烷基糖苷柠檬酸酯 *

Also Published As

Publication number Publication date
CN108179073A (en) 2018-06-19

Similar Documents

Publication Publication Date Title
CN104673546A (en) Camellia oil handmade soap
CN108179073B (en) Mild bactericidal laundry detergent and preparation method thereof
CN101935358A (en) Ganoderma lucidum polysaccharide and preparation method thereof
CN105326706A (en) Hand sanitizer containing camellia seed cake extract and preparation method thereof
CN103830744A (en) Sustained release gallogen-cyclodextrin compound and preparation method thereof
CN101570555A (en) Preparation method of calcium supplement carboxymethyl chitosan oligosaccharide calcium
CN112430510B (en) Bacteriostatic detergent containing plant surfactant and preparation method thereof
CN107164828B (en) Preparation method of cereal protein modified functional fiber
CN102634421B (en) laundry detergent and preparation method thereof
CN108383945A (en) A kind of agricultural water-loss reducer and preparation method thereof
CN107177643B (en) Tremella residue fermentation product, skin-care washing product containing fermentation product and preparation method of skin-care washing product
CN104479926A (en) Natural plant detergent and preparation method thereof
CN105907820A (en) Method for extracting hyaluronic acid in squid eyes with fermentation method
CN102552065B (en) Carboxymethyl yeast dextran eye cream, preparation method and application thereof
CN105106108A (en) Supermolecule controlled/slow-release type salicylate formula and preparation technology thereof
CN113318021B (en) Hand sanitizer
CN101570554A (en) Method for preparing zinc supplementing agent carboxymethyl chitosan oligosaccharide zinc
CN101768582A (en) Production process for modifying SOD
JPH0157958B2 (en)
CN102525859B (en) Carboxymethyl yeast glucan emulsion as well as preparation method and application thereof
CN106434516A (en) Preparation method and application for edible fungus selenium-enriched polysaccharide
CN105147596A (en) Water-soluble supramolecular salicylic acid gel technology
CN106148450A (en) A kind of high yield zinc-rich biological cellulose gel product
CN102995403A (en) Method for solidifying high-performance chitosan on fabric
CN115770203B (en) Modified jojoba oil and preparation method and application thereof

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
GR01 Patent grant
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20200515