CN111117811A - Cleaning composition for removing odor of fabrics dried in the shade - Google Patents

Cleaning composition for removing odor of fabrics dried in the shade Download PDF

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Publication number
CN111117811A
CN111117811A CN201911377302.XA CN201911377302A CN111117811A CN 111117811 A CN111117811 A CN 111117811A CN 201911377302 A CN201911377302 A CN 201911377302A CN 111117811 A CN111117811 A CN 111117811A
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mass
parts
cleaning composition
surfactant
test
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孙璐璐
潘莹莹
张世新
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Shanghai Jahwa United Co Ltd
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Shanghai Jahwa United Co Ltd
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Priority to CN201911377302.XA priority Critical patent/CN111117811A/en
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    • 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
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/94Mixtures with anionic, cationic or non-ionic 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/201Monohydric alcohols linear
    • 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
    • C11D3/24Organic compounds containing halogen
    • 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
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/32Amides; Substituted amides
    • C11D3/323Amides; Substituted amides urea or derivatives thereof
    • 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
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/33Amino carboxylic acids
    • 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
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38618Protease or amylase in liquid compositions only
    • 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
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38627Preparations containing enzymes, e.g. protease or amylase containing lipase
    • 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
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38645Preparations containing enzymes, e.g. protease or amylase containing cellulase
    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/50Perfumes
    • 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
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic 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
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/72Ethers of polyoxyalkylene glycols
    • 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
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/92Sulfobetaines ; Sulfitobetaines

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  • 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)
  • Detergent Compositions (AREA)

Abstract

A cleaning composition for removing the shade-dried odor of fabrics comprising: 15-65% by weight of a surfactant; 0.01-2% by weight of a bactericide; 0.05-3 wt% of essence; 0.1-2 wt% of an enzyme; 1-10 wt% of a chelating agent; and a carrier acceptable in the field of fabric cleaning, wherein the surfactant is selected from the group consisting of: a non-ionic surfactant, an anionic surfactant, a zwitterionic surfactant, or a combination thereof, wherein the enzyme is a mixture of a protease, a lipase, and a cellulase. The invention also relates to a method for removing the shade-dried odor of the fabric.

Description

Cleaning composition for removing odor of fabrics dried in the shade
Technical Field
The invention relates to the field of household chemicals, and discloses a cleaning product capable of removing the peculiar smell of fabrics dried in the shade in multiple effects.
Background
In rainy days in the south of China, particularly in plum rain in the middle and downstream areas of Yangtze river, unpleasant peculiar smell is easily generated when clothes are dried in the shade. At present, the odor-removing laundry detergent is on the market, but the effect is poor.
The daily chemical products are added in many times, and the market competition of the fabric care is very strong at present, especially the laundry detergent market. In order to meet the requirements of different consumers, various large brands develop laundry detergents with different concept declarations and additional functions.
We find that in rainy days in the south China, especially in plum rain in the middle and lower reaches of Yangtze river, clothes are easy to generate unpleasant peculiar smell when dried in the shade. If a fabric care product such as a laundry detergent is developed that can remove this odor and suppress its generation, it should be able to be used in a competitive market.
Heretofore, there is no laundry detergent technology that can effectively remove the odor of the drying in the shade. The invention aims to provide a technical scheme which can remove the drying odor of clothes in the shade and inhibit the generation of the drying odor in all directions, thereby solving the trouble of consumers.
Disclosure of Invention
In one aspect, the present invention provides a cleaning composition for removing the shade-dried odor of fabrics, comprising:
15-65% by weight of a surfactant;
0.01-2% by weight of a bactericide;
0.05-3 wt% of essence;
0.1-2 wt% of an enzyme;
1-10 wt% of a chelating agent; and
a carrier that is acceptable in the field of fabric cleaning,
wherein the surfactant is selected from: a non-ionic surfactant, an anionic surfactant, a zwitterionic surfactant, or a combination thereof,
wherein the enzyme is a mixture of protease, lipase and cellulase.
In a preferred embodiment, the cleaning composition of the present invention further comprises a deodorant. In a more preferred embodiment, the odor-reducing agent in the cleaning composition of the present invention is a plant odor-reducing agent. For example, fabric malodor-reducing agents may be used in amounts up to about 2% by weight.
In a preferred embodiment, the surfactant in the cleaning composition of the present invention is selected from the group consisting of: sodium fatty alcohol polyoxyethylene ether sulfate, polyoxyethylene fatty alcohol ether, sodium dodecyl benzene sulfonate, cocamidopropyl hydroxysultaine, fatty acid methyl ester ethoxylate or their combination.
In a preferred embodiment, the bactericide in the cleaning composition of the present invention is selected from the group consisting of: triclosan, triclocarban, p-chloro-m-xylenol, or combinations thereof.
In a preferred embodiment, the perfume in the cleaning composition of the present invention is selected from the group consisting of: free oil flavors, microencapsulated flavors, or a combination thereof.
In a preferred embodiment, the enzyme is present in the cleaning composition of the present invention at about 0.2 wt%.
In a preferred embodiment, the cleaning composition of the present invention further comprises an adjunct acceptable in the fabric cleaning art.
In another aspect, the present invention is also directed to a method for deodorizing fabrics from drying in the shade comprising contacting the fabrics with an effective amount of the cleaning composition of the present invention.
In a preferred embodiment, the contacting step is performed in a wash cycle of a manual wash or an automatic washing machine.
Detailed Description
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are described herein. For the purposes of the present invention, the following terms are defined below.
The term "about" as used herein refers to an amount, level, value, dimension, size, or amount that differs by up to 30%, 20%, or 10% as compared to the amount, level, value, dimension, size, or amount of a reference. The percentages used herein are by weight unless otherwise indicated.
Throughout the specification and claims, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
Aiming at the problem of clothes drying in the shade and peculiar smell, the invention treats both symptoms and root causes, and creatively adopts the combination of a surfactant, a bactericide, essence, enzyme and a plant deodorant to realize unexpected technical effects. The cleaning compositions of the present invention may be applied using any carrier acceptable in the art of fabric cleaning. In a preferred embodiment, the cleaning compositions of the present invention employ an aqueous carrier. For example, the carrier is water, e.g., pure water, distilled water, deionized water, and the like.
The cleaning composition of the present invention can remove odor-causing bacteria including Oersura (ATCC19976), Staphylococcus epidermidis (ATCC12228) and Corynebacterium jejuni (ATCC43734), and has excellent detergency to further eradicate the generation of odor source.
Specifically, ① focuses on the Oersura strain with the largest influence among three strains (Oersura strain, Staphylococcus epidermidis and Corynebacterium jejuni) which are possibly metabolized to generate the dry odor, and the most effective and intuitive bacteria inhibition ring experiment is finally selected through different bacteria removal test methods (ATP simulation experiment and bacteria inhibition ring experiment), and the result shows that the bacteria removal effect of the preferred laundry detergent is obviously superior to that of a competitive product, ② uncleaned dirt on clothes is beneficial to the growth of the Oersura strain, so the improved detergency is also a means for radically treating the dry odor of the laundry detergent, and the detergency of the preferred laundry detergent screened by the formula is superior to that of the competitive product.
On the other hand, the cleaning composition of the invention can effectively prevent and reduce the perception of peculiar smell by consumers, and realize the effect of removing the peculiar smell. Meanwhile, by adding the plant smell removing agent, clothes with heavy drying peculiar smell can be effectively removed.
Specifically, ① can effectively prevent and reduce the perception of the peculiar smell of the consumers through a new generation of essence technology, and the result shows that the odor removing effect of the preferred laundry detergent is obviously superior to that of a competitive product through the cooperation test with an essence company. ② not only meets the green trend, but also can effectively remove clothes with heavy drying peculiar smell before washing and reduce the possibility of aggravating the peculiar smell after washing by adding the plant odor removing agent.
Surface active agent
The cleaning composition according to the present invention comprises a surfactant, more preferably a detersive surfactant. Detersive surfactant means a surfactant that provides soil release (i.e., cleaning effect) to the textile fabric being treated as part of the cleaning process, preferably a laundry process.
Preferably, the total amount of surfactant present in the cleaning composition is from 15 to 65 wt.%, more preferably from 15 to 50 wt.%, more preferably from 15 to 40 wt.%, still even more preferably from 15 to 30 wt.%, still even more preferably from 20 to 30 wt.%.
Preferably, the detersive surfactant comprises a nonionic surfactant, an anionic surfactant, a zwitterionic surfactant or a mixture thereof, more preferably a nonionic surfactant, an anionic surfactant and a zwitterionic surfactant.
Unless otherwise indicated, "nonionic surfactant" is defined as an amphiphilic molecule having a molecular weight of less than about 10,000 that is substantially free of any functional groups that exhibit a net charge at normal wash pH of 6-11. Preferably, the amount of nonionic surfactant is from 1 to 30 wt%, more preferably from 5 to 30 wt%, even more preferably from 10 to 20 wt%.
Any type of nonionic surfactant can be used. The nonionic surfactant is preferably a fatty acid alkoxylate, more preferably an ethoxylate. Preferred ethoxylates have alkyl chains of C8-C35, more preferably C10-C24; and preferably has 3 to 25, more preferably 5 to 15 ethylene oxide groups. Suitable nonionic surfactants include alcohol ethoxylates (AE or AEO), alcohol propoxylates, Propoxylated Fatty Alcohols (PFA), alkoxylated fatty acid alkyl esters such as ethoxylated and/or propoxylated fatty acid alkyl esters, alkylphenol ethoxylates (APE), nonylphenol ethoxylates (NPE), Alkylpolyglycosides (APG), alkoxylated amines, Fatty Acid Monoethanolamides (FAM), Fatty Acid Diethanolamides (FADA), Ethoxylated Fatty Acid Monoethanolamides (EFAM), Propoxylated Fatty Acid Monoethanolamides (PFAM), polyhydroxyalkyl fatty acid amides, or N-acyl N-alkyl derivatives of glucosamine (glucamide GA or fatty acid glucamide FAGA), as well as products available under the trade names SPAN and TWEEN, and combinations thereof. Preferred nonionic surfactants are C12-C18 ethoxylated alcohols containing 3 to 9 ethylene oxide units per molecule. More preferred are C12-C15 linear ethoxylated primary alcohols having an average of 5 to 9 ethylene oxide groups, more preferably an average of 7 ethylene oxide groups.
In a particular embodiment, the cleaning composition of the present invention comprises a nonionic surfactant that is a polyoxyethylene fatty alcohol ether.
An "anionic surfactant" is defined as an amphiphilic molecule comprising one or more functional groups which exhibit a net anionic charge at normal wash pH between 6 and 11 when in aqueous solution. Preferably, the amount of anionic surfactant is from 1 to 15 wt%, more preferably from 1 to 10 wt%, even more preferably from 1 to 5 wt%.
Preferred anionic surfactants are alkali metal salts of organic sulfur reaction products having in their molecular structure an alkyl group containing from about 6 to 24 carbon atoms and a group selected from the group consisting of sulfonic and sulfuric acid ester groups. More preferred anionic surfactants are the following alkali and alkaline earth metal salts: fatty acid carboxylic acids, fatty alcohol sulfuric acids, preferably primary alkyl sulfuric acids, more preferably they are ethoxylated, for example alkyl ether sulfuric acids; and alkyl benzene sulphonic acid or mixtures thereof.
Non-limiting examples of anionic surfactants include sulfates and sulfonates, particularly Linear Alkylbenzene Sulfonate (LAS), isomers of LAS, branched alkylbenzene sulfonate (BABS), phenyl alkane sulfonate, α -olefin sulfonate (AOS), olefin sulfonate, alkane-2, 3-diylbis (sulfate), hydroxyalkyl sulfonate and disulfonate, Alkyl Sulfate (AS) such AS Sodium Dodecyl Sulfate (SDS), Fatty Alcohol Sulfate (FAS), Primary Alcohol Sulfate (PAS), alcohol ether sulfate (AES or AEOS or FES, also known AS alcohol ethoxy sulfate or fatty alcohol ether sulfate), Secondary Alkane Sulfonate (SAS), Paraffin Sulfonate (PS), ester sulfonate, sulfonated fatty acid glycerides, α -sulfonated fatty acid methyl ester including Methyl Ester Sulfonate (MES) (α -SFMe or SES), alkyl or alkenyl succinic acid, dodecenyl/tetradecenyl succinic acid (DTSA), fatty acid derivatives of amino acids, diesters and monoesters of sulfosuccinic acid or soap, and combinations thereof.
In a particular embodiment, the cleaning composition of the present invention comprises an anionic surfactant that is sodium fatty alcohol polyoxyethylene ether sulfate, sodium dodecyl benzene sulfonate, or a combination thereof.
Unless otherwise indicated, a "zwitterionic surfactant" is a molecule that contains both acidic and basic groups and will exist as a zwitterion at normal wash pH between 6 and 11. Preferably, the amount of zwitterionic surfactant is from 1 to 15 wt%, more preferably from 1 to 10 wt%, even more preferably from 1 to 5 wt%.
Preferred amphoteric or zwitterionic surfactants are betaine surfactants. More preferably, they are one or more of the following list: sulfatobetaines, such as 3- (dodecyldimethylammonium) -1-propane sulfate; and 2- (cocodimethylammonium) -1-ethane sulfate. Sulfobetaines, such as: 3- (dodecyl dimethyl ammonium) -2-hydroxy-1-propane sulfonate; 3- (tetradecyldimethylammonium) -1-propanesulfonate; 3- (C12-C14 alkylamidopropyldimethylammonium) -2-hydroxy-1-propanesulfonic acid salt; and 3- (cocodimethylammonium) -1-propane sulfonate. Carboxybetaines, such as (dodecyl dimethyl ammonium) acetate (also known as lauryl betaine); (tetradecyldimethylammonium) acetate (also known as cinnamyl betaine); (cocodimethylammonium) acetate (also known as cocobetaine); (oleyldimethylammonium) acetate (also known as oleylbetaine); (dodecyloxymethyldimethylammonium) acetate; and (cocamidopropyl dimethyl ammonium) acetate (also known as cocamidopropyl betaine or CAPB). Sulfonium betaines, such as: (dodecyl dimethyl sulfonium) acetate; and 3- (cocodimethylsulfonium) -1-propane sulfonate. Phosphonium betaines, such as 4- (trimethylphosphonium) -1-hexadecane sulfonate; 3- (dodecyl dimethyl phosphonium) -1-propane sulfonate; and 2- (dodecyldimethylphosphonium) -1-ethanesulfate.
In a particular embodiment, the zwitterionic surfactant comprised by the cleaning composition of the present invention is cocamidopropyl hydroxysultaine.
In a preferred embodiment, a combination of non-ionic, anionic and zwitterionic surfactants is used. If a combination of nonionic, anionic and zwitterionic surfactants is used, the nonionic surfactant is preferred: anionic surfactant: the ratio of zwitterionic surfactant was 16:4: 3.
Bactericide
The cleaning composition according to the present invention comprises a bactericide.
In a preferred embodiment, the biocide is selected from: triclosan, triclocarban, parachlorometaxylenol, blumea oil, licorice root extract, or combinations thereof. In a more preferred embodiment, the biocide is selected from: triclosan, triclocarban, p-chloro-m-xylenol, or combinations thereof.
In a preferred embodiment, the amount of biocide present in the cleaning composition of the invention is from 0.01 to 2 wt.%, more preferably from 0.01 to 0.1 wt.%, more preferably from 0.01 to 0.5 wt.%. In a specific embodiment, the amount of biocide present in the cleaning composition of the present invention is 0.06 wt%. In another specific embodiment, the disinfectant is present in the cleaning composition of the present invention in an amount of 0.3 wt%.
Essence
The cleaning compositions of the present invention comprise perfume. The perfume may be provided as a free oil and/or in microcapsules.
The cleaning compositions of the present invention may comprise one or more perfumes. The fragrance may be in the form of a mixture or free fragrance, a mixture of encapsulated fragrances or a mixture of encapsulated and free oil fragrances.
A fragrance in the form of a free oil may be added to the cleaning composition. These perfumes may impart an odor to the cleaning composition, provide an odor during the laundering process or provide an odor to fabrics after laundering.
The free perfume may preferably be present in an amount of from 0.05 to 3 wt%, more preferably from 0.05 to 1 wt%, even more preferably from 0.05 to 0.75 wt%, most preferably from 0.55 to 0.75 wt%, based on the total weight of the composition.
When the perfume is in a microcapsule, suitable encapsulating materials may include, but are not limited to; aminoplasts, proteins, polyurethanes, polyacrylates, polymethacrylates, polysaccharides, polyamides, polyolefins, gums, silicones, lipids, modified celluloses, polyphosphates, polystyrenes, polyesters, or combinations thereof.
The microencapsulated flavour may preferably be present in an amount of from 0.05 to 3 wt%, more preferably from 0.05 to 1 wt%, even more preferably from 0.05 to 0.75 wt%, most preferably from 0.55 to 0.75 wt%, based on the total weight of the composition.
A combination of perfume in free oil form with microencapsulated perfume may also be used in the cleaning compositions of the present invention. The combined fragrances may preferably be present in an amount of from 0.05 to 3 wt%, more preferably from 0.05 to 1 wt%, even more preferably from 0.05 to 0.75 wt%, most preferably from 0.55 to 0.75 wt%, based on the total weight of the composition.
In a particular embodiment, the perfume used in the cleaning composition of the present invention is P15P822 ISLAND available from phenmei company. In a particular embodiment, the fragrance used in the cleaning composition of the present invention is powerul popsant P52G708 available from phenmei. In a particular embodiment, the fragrance used in the cleaning compositions of the present invention is FRESH DEW P95L369 available from phenmei corporation.
Enzyme
The cleaning composition according to the invention comprises an enzyme.
In a preferred embodiment, the enzyme is selected from the group consisting of: a protease, a lipase, an amylase, a cellulase, or a combination thereof.
In a preferred embodiment, the amount of enzyme present in the cleaning composition of the invention is from 0.1 to 2 wt.%, more preferably from 0.1 to 1 wt.%, more preferably from 0.1 to 0.5 wt.%. In a particular embodiment, the amount of enzyme present in the cleaning composition of the present invention is 0.2 wt%.
In a particular embodiment, the enzyme used in the cleaning composition of the present invention is available from Medley SmartR100L available from novetin.
Smell eliminating agent
The cleaning composition according to the invention optionally further comprises an odor eliminator. In a preferred embodiment, the odor-reducing agent is a plant odor-reducing agent.
In a preferred embodiment, the content of the odor eliminating agent in the cleaning composition of the present invention is 0 to 10% by weight, more preferably 0 to 5% by weight, more preferably 1 to 2% by weight.
In a specific embodiment, the odor eliminating agent used in the cleansing composition of the present invention is TH-70 available from Sanchen, Kunming. In a specific embodiment, the odor eliminator used in the cleansing compositions of the present invention is air receptor (r) 198, available from kunshinan corporation.
Other ingredients
The cleaning compositions of the present invention may also comprise other ingredients.
Preferably, the cleaning composition of the present invention comprises up to 10 wt%, more preferably up to 5 wt% of a chelating agent, examples of chelating agents are N- (1, 2-dicarboxyethyl) -D, L-aspartic acid (IDS), N- (2-hydroxyethyl) iminodiacetic acid (EDG), aspartic acid-N-monoacetic acid (ASMA), aspartic acid-N, N-diacetic acid (ASDA), aspartic acid-N-monopropionic Acid (ASMP), iminodisuccinic acid (IDA), N- (2-sulfomethyl) aspartic acid (SMAS), N- (2-sulfoethyl) aspartic acid (SEAS), N- (2-sulfomethyl) glutamic acid (SMGL), N- (2-sulfoethyl) glutamic acid (SEGL), N-methyliminodiacetic acid (MIDA), α -alanine-N, N-diacetic acid (α -ALDA), serine-N, N-diacetic acid (SEDA), isoserine-N, N-diacetic acid (ISDA), phenylalanine-N, N-diacetic acid (PHDA), orthophosphonic acid (PHDA), N-ethylenediaminetetraacetic acid (edta), N-ethylenediamine tetraacetic acid (edta), N-hydroxyethylenediaminic acid (1, N-hydroxyethylphosphonic acid (edta), as another embodiment of the cleaning composition, as used herein.
The cleaning compositions of the present invention also preferably comprise a hydrotrope. Hydrotropes are compounds that solubilize hydrophobic compounds in aqueous solution (or conversely, polar materials in a non-polar environment). The use of a hydrotrope in the cleaning composition allows for more concentrated formulation of, for example, surfactants (e.g., during densification of the cleaning composition by removal of water) without causing undesirable phenomena such as phase separation or high viscosity. The cleaning composition can contain 0-5 wt.%, such as about 0.5 to about 5 wt.%, or about 3% to about 5 wt.% of a hydrotrope. Any hydrotrope known in the art for use in cleaning compositions can be used. Non-limiting examples of hydrotropes include: sodium benzene sulfonate, sodium p-toluene sulfonate (STS), Sodium Xylene Sulfonate (SXS), Sodium Cumene Sulfonate (SCS), sodium cymene sulfonate, Amine Oxide (AO), alcohol and polyglycol ether, sodium hydroxynaphthalene formate, sodium hydroxynaphthalene sulfonate, sodium ethylhexyl sulfate, and combinations thereof.
The cleaning compositions of the present invention also preferably comprise builders, more preferably one or more of aluminosilicate materials, silicates, polycarboxylates and fatty acids, materials such as edetate, metal ion sequestrants such as aminopolyphosphonates. Even more preferably, the cleaning composition according to the present invention comprises zeolite a, citric acid or a combination thereof. The amount of builder is preferably from 0 to 35 wt%, more preferably from 1 to 20 wt%, even more preferably from 5 to 15 wt%.
The cleaning compositions of the present invention are also preferably suds suppressors, more preferably silica-based suds suppressors, silicon-based suds suppressors, or mixtures thereof. Even more preferably, the cleaning composition according to the invention comprises a mixture of silicone oil and 2-alkyl alkanol. Silicone refers to an alkylated polysiloxane material. The silicas are preferably used in finely divided form, for example various types of silica aerogels and xerogels and hydrophobic silicas. Preferably, the suds suppressor is present in an amount of from 0.001 to 2% by weight, more preferably from 0.01 to 1% by weight.
Preferably, the cleaning composition according to the present invention comprises methylcellulose, carboxymethylcellulose and hydroxyethylcellulose and one or more antiredeposition agents (also known as soil suspending agents) of homo-or copolymeric polycarboxylic acids or salts thereof. Preferably, the amount of anti-redeposition agent is 0.5 to 10 wt%, more preferably 0.75 to 8 wt%, even more preferably 1 to 6 wt%.
Preferably, the cleaning compositions according to the present invention comprise one or more soil release agents, more preferably copolymers or terpolymers of terephthalic acid with ethylene glycol and/or propylene glycol units in various arrangements.
The cleaning composition may comprise other ingredients commonly found in detergent liquids. Preferably, the cleaning composition according to the present invention further comprises one or more of a sunscreen agent, a colorant, a softener, an antioxidant, a pH control agent and a buffer.
Method for cleaning fabrics
The present invention also relates to a method of deodorizing fabrics dried in the shade comprising contacting said fabrics with an effective amount of the cleaning composition of the present invention.
In preferred embodiments, the contacting of the fabric with the cleaning composition can be carried out in a manual wash or in the wash cycle of an automatic washing machine.
Detailed Description
The technical aspects of the present invention will be described in detail below with reference to preferred embodiments, but the scope of the present invention is not limited to these embodiments, and the technical aspects of the present invention are intended to be described and not limited. Test methods in which specific conditions are not specified in the following examples are generally carried out under conventional conditions or under conditions recommended by the manufacturer. All percentages and parts are by weight unless otherwise indicated.
The ingredients and sources of the individual raw materials employed in the following examples are as follows:
sodium fatty alcohol polyoxyethylene ether sulfate, available from Zhejiang Zanyu corporation;
polyoxyethylene fatty alcohol ethers, available from zhu, zan, chem, inc;
sodium dodecylbenzenesulfonate, available from zhu, zan, zhejiang;
cocamidopropyl hydroxysultaine, available from guangzhou star industries;
disodium edetate, available from aksunobel corporation;
tetrasodium glutamate diacetate, available from aksonobel corporation;
medley SmartR100L, available from Novixin;
dichloro, available from BASF corporation;
triclosan, available from Shanghai Lisheng company;
triclocarban, available from hangzhou de gao;
para-chloro-meta-xylenol available from Jiangsu Huanxin;
blumea oil, available from biotechnology limited of Yunnan England;
the licorice extract is purchased from Shanghai family Biotechnology Co., Ltd;
alcohol, purchased from Jiangsu Hua Hall Co
P15P822 ISLAND, available from phenmei inc;
POWERFUL POPSCENT P52G708 available from Fineley corporation;
FRESH DEW P95L369 available from Fenmeiyi;
TH-70, purchased from Kun Cheng corporation;
AIRKEM198, available from KUNXUESHAN;
the musty simulant, trade name musty simulant, was purchased from Fenmeiyi.
Example 1: preparation of Fabric cleaning compositions
Weighing 71.8 parts by mass of deionized water, placing the deionized water into a beaker, sequentially adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, 6 parts by mass of polyoxyethylene fatty alcohol ether, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine under the stirring state at the rotating speed of 400rpm, and stirring until the mixture is clear and transparent. Then 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and stirred until the mixture is clear and transparent for later use.
Example 2: preparation of Fabric cleaning compositions
Firstly, 0.3 part by mass of dichloro is dissolved in 6 parts by mass of polyoxyethylene fatty alcohol ether to prepare small materials. Weighing 71.5 parts by mass of deionized water, placing the deionized water into a beaker, sequentially adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine under the stirring state at the rotating speed of 400rpm, and stirring until the mixture is clear and transparent. Then 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of MedleySmartR 100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 3: preparation of Fabric cleaning compositions
Firstly, 0.3 part by mass of triclosan is dissolved in 6 parts by mass of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 4: preparation of Fabric cleaning compositions
Dissolving 0.3 mass part of triclocarban in 6 mass parts of polyoxyethylene fatty alcohol ether to prepare a small material. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 5: preparation of Fabric cleaning compositions
Firstly, 0.3 part by mass of parachlorometaxylenol is dissolved in 6 parts by mass of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 6: preparation of Fabric cleaning compositions
Firstly, 0.3 part by mass of blumea oil is dissolved in 6 parts by mass of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 7: preparation of Fabric cleaning compositions
Firstly, 0.3 part by mass of liquorice extract is dissolved in 6 parts by mass of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 8: preparation of Fabric cleaning compositions
Firstly, 0.15 mass part of triclosan and 0.15 mass part of triclocarban are dissolved in 6 mass parts of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of MedleySmartR 100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 9: preparation of Fabric cleaning compositions
Firstly, 0.15 mass part of triclosan and 0.15 mass part of parachlorometaxylenol are dissolved in 6 mass parts of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 10: preparation of Fabric cleaning compositions
Firstly, 0.15 mass part of triclocarban and 0.15 mass part of parachlorometaxylenol are dissolved in 6 mass parts of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 11: preparation of Fabric cleaning compositions
Firstly, 0.15 mass part of dichloro is dissolved in 6 mass parts of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 12: preparation of Fabric cleaning compositions
Firstly, 0.06 part by mass of dichloro is dissolved in 6 parts by mass of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 13: preparation of Fabric cleaning compositions
Firstly, 0.06 part by mass of triclosan and 0.24 part by mass of parachlorometaxylenol are dissolved in 6 parts by mass of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 14: preparation of Fabric cleaning compositions
Firstly, 0.15 mass part of dichlorotoluene and 0.15 mass part of parachlorometaxylenol are dissolved in 6 mass parts of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then, 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added, and the mixture is stirred until the mixture is clear and transparent for later use.
Example 15: preparation of Fabric cleaning compositions
Firstly, 0.06 part by mass of triclosan and 10 parts by mass of alcohol are dissolved in 6 parts by mass of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added and stirred until the mixture is clear and transparent for later use.
Example 16: preparation of Fabric cleaning compositions
Firstly, 0.06 part by mass of triclosan and 5 parts by mass of alcohol are dissolved in 6 parts by mass of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added and stirred until the mixture is clear and transparent for later use.
Example 17: preparation of Fabric cleaning compositions
Firstly, 0.06 part by mass of triclosan and 1 part by mass of alcohol are dissolved in 6 parts by mass of polyoxyethylene fatty alcohol ether to prepare small materials. Adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine into 71.5 parts by mass of deionized water in sequence under a stirring state, and stirring until the mixture is clear and transparent. Then 5 parts by mass of disodium ethylene diamine tetraacetate and 0.2 part by mass of Medley SmartR100L enzyme are added and stirred until the mixture is clear and transparent for later use.
Table 1 summarizes the types and amounts of the biocides used in examples 1-17.
Figure BDA0002341337050000171
Test example 1: zone of inhibition detection
Detecting a sample: examples 1-17 Effect of Fabric cleaning compositions on Oersura ATCC19976
Preparing the bacteriostatic tablets:
for liquid bacteriostat, a sterile and dry filter paper sheet is taken. Dripping 20 μ l of bacteriostatic agent solution with practical use concentration into each piece, placing the filter paper piece in a clean sterile plate, opening the cover, and oven drying in a warm box (37 deg.C), or naturally drying at room temperature for use.
The dissoluble antibacterial product can be directly made into round pieces (blocks) with the diameter of 5mm and the thickness of not more than 4mm, and every 4 round pieces (blocks) are in a group.
Preparation of negative control sample: taking a sterile dry filter paper sheet, dripping 20 mu l of sterile distilled water into each sheet, and drying for later use.
The negative control sample of the dissoluble antibacterial product is prepared by taking a sample which is made of the same material and does not contain the antibacterial component, and preparing a sample slice (block) with the same size as the test group.
Inoculation of test bacteria: dipping with sterile cotton swab to 5 × 10 concentration5cfu/ml~5×106cfu/ml test bacterial suspension was evenly spread on the surface of nutrient agar medium plate for 3 times. For each application 1 time, the plate should be rotated 60 °, and finally the cotton swab is applied around the edge of the plate for one revolution. The plate was covered and left to dry at room temperature for 5 minutes (min).
Sticking bacteriostatic agent sample pieces: each test is stuck with 1 infectious bacterium plate, and each plate is stuck with 4 test sample plates and 1 negative control sample plate, and the number of the negative control sample plates is 5. A sample was taken with sterile forceps and placed on the surface of the plate. The distance between the centers of the various pieces is more than 25mm, and the distance between the centers of the various pieces and the periphery of the flat plate is more than 15 mm. After the sample is placed, the sample is lightly pressed by using sterile tweezers to be tightly attached to the surface of the flat plate. The plate is covered, the plate is placed in an incubator at 37 ℃, and the result is observed after the plate is cultured for 16 to 18 hours. The diameter of the antibacterial ring (including the patch) was measured with a vernier caliper and recorded. The experiment was repeated 3 times.
When the inhibition zone is measured, the inhibition zone which is uniform and completely aseptically grows is selected for measurement. The diameter of the catheter is measured by taking the outer edge of the bacteriostatic ring as a boundary.
The evaluation rules are:
judging the bacteriostatic action:
if the diameter of the bacteriostatic ring is larger than 7mm, the bacteriostatic ring is judged to have bacteriostatic action.
If the diameter of the antibacterial ring is less than or equal to 7mm, the product is judged to have no antibacterial effect.
And 3 times of repeated tests show that the product has the bacteriostatic effect, and the product is judged to be qualified.
The negative control group should have no bacteriostatic ring. Otherwise the test is invalid.
The results are shown in Table 2.
TABLE 2
Figure BDA0002341337050000191
The results show that all the examples have bacteriostatic effect, and the bacteriostatic ring is larger than 7 mm. However, the ideal bacteriostatic ring in the application needs to be more than or equal to 40mm to meet the invention requirements, so the bacteriostatic effect is the best in examples 2,3 and 9, the bacteriostatic effect is better in examples 5, 8, 11, 12, 13, 14, 15, 16 and 17, and the bacteriostatic effect is general in examples 1, 4, 6, 7 and 10.
Test example 2: zone of inhibition detection
Detecting a sample: examples 1-6 Effect of Fabric cleaning compositions on Staphylococcus epidermidis ATCC12228
Preparing the bacteriostatic tablets:
for liquid bacteriostat, a sterile and dry filter paper sheet is taken. Dripping 20 μ l of bacteriostatic agent solution with practical use concentration into each piece, placing the filter paper piece in a clean sterile plate, opening the cover, and oven drying in a warm box (37 deg.C), or naturally drying at room temperature for use.
The dissoluble antibacterial product can be directly made into round pieces (blocks) with the diameter of 5mm and the thickness of not more than 4mm, and every 4 round pieces (blocks) are in a group.
Preparation of negative control sample: taking a sterile dry filter paper sheet, dripping 20 mu l of sterile distilled water into each sheet, and drying for later use.
The negative control sample of the dissoluble antibacterial product is prepared by taking a sample which is made of the same material and does not contain the antibacterial component, and preparing a sample slice (block) with the same size as the test group.
Inoculation of test bacteria: dipping with sterile cotton swab to 5 × 10 concentration5cfu/ml~5×106cfu/ml test bacterial suspension was evenly spread on the surface of nutrient agar medium plate for 3 times. For each application 1 time, the plate should be rotated 60 °, and finally the cotton swab is applied around the edge of the plate for one revolution. The plate was covered and dried at room temperature for 5 min.
Sticking bacteriostatic agent sample pieces: each test is stuck with 1 infectious bacterium plate, and each plate is stuck with 4 test sample plates and 1 negative control sample plate, and the number of the negative control sample plates is 5. A sample was taken with sterile forceps and placed on the surface of the plate. The distance between the centers of the various pieces is more than 25mm, and the distance between the centers of the various pieces and the periphery of the flat plate is more than 15 mm. After the sample is placed, the sample is lightly pressed by using sterile tweezers to be tightly attached to the surface of the flat plate. The plate is covered, the plate is placed in an incubator at 37 ℃, and the result is observed after the plate is cultured for 16 to 18 hours. The diameter of the antibacterial ring (including the patch) was measured with a vernier caliper and recorded. The experiment was repeated 3 times.
When the inhibition zone is measured, the inhibition zone which is uniform and completely aseptically grows is selected for measurement. The diameter of the catheter is measured by taking the outer edge of the bacteriostatic ring as a boundary.
The evaluation rules are:
judging the bacteriostatic action:
if the diameter of the bacteriostatic ring is larger than 7mm, the bacteriostatic ring is judged to have bacteriostatic action.
If the diameter of the antibacterial ring is less than or equal to 7mm, the product is judged to have no antibacterial effect.
And 3 times of repeated tests show that the product has the bacteriostatic effect, and the product is judged to be qualified.
The negative control group should have no bacteriostatic ring. Otherwise the test is invalid.
The results are shown in Table 3.
TABLE 3
Figure BDA0002341337050000201
The results show that all the examples have bacteriostatic effect, and the bacteriostatic ring is larger than 7 mm. The ideal bacteriostatic ring in the application needs to be more than or equal to 40mm to meet the invention requirements, so the embodiments 2 and 3 have better bacteriostatic effect, the embodiment 4 has good bacteriostatic effect, the embodiment 1 has general bacteriostatic effect, and the embodiments 5 and 6 have qualified bacteriostatic effect.
Test example 3: zone of inhibition detection
Detecting a sample: EXAMPLES 1-6 Effect of Fabric cleaning compositions on Corynebacterium jeikeium ATCC43734
Preparing the bacteriostatic tablets:
for liquid bacteriostat, a sterile and dry filter paper sheet is taken. Dripping 20 μ l of bacteriostatic agent solution with practical use concentration into each piece, placing the filter paper piece in a clean sterile plate, opening the cover, and oven drying in a warm box (37 deg.C), or naturally drying at room temperature for use.
The dissoluble antibacterial product can be directly made into round pieces (blocks) with the diameter of 5mm and the thickness of not more than 4mm, and every 4 round pieces (blocks) are in a group.
Preparation of negative control sample: taking a sterile dry filter paper sheet, dripping 20 mu l of sterile distilled water into each sheet, and drying for later use.
The negative control sample of the dissoluble antibacterial product is prepared by taking a sample which is made of the same material and does not contain the antibacterial component, and preparing a sample slice (block) with the same size as the test group.
Inoculation of test bacteria: dipping with sterile cotton swab to 5 × 10 concentration5cfu/ml~5×106cfu/ml test bacterial suspension was evenly spread on the surface of nutrient agar medium plate for 3 times. For each application 1 time, the plate should be rotated 60 °, and finally the cotton swab is applied around the edge of the plate for one revolution. The plate was covered and dried at room temperature for 5 min.
Sticking bacteriostatic agent sample pieces: each test is stuck with 1 infectious bacterium plate, and each plate is stuck with 4 test sample plates and 1 negative control sample plate, and the number of the negative control sample plates is 5. A sample was taken with sterile forceps and placed on the surface of the plate. The distance between the centers of the various pieces is more than 25mm, and the distance between the centers of the various pieces and the periphery of the flat plate is more than 15 mm. After the sample is placed, the sample is lightly pressed by using sterile tweezers to be tightly attached to the surface of the flat plate. The plate is covered, the plate is placed in an incubator at 37 ℃, and the result is observed after the plate is cultured for 16 to 18 hours. The diameter of the antibacterial ring (including the patch) was measured with a vernier caliper and recorded. The experiment was repeated 3 times.
When the inhibition zone is measured, the inhibition zone which is uniform and completely aseptically grows is selected for measurement. The diameter of the catheter is measured by taking the outer edge of the bacteriostatic ring as a boundary.
The evaluation rules are:
judging the bacteriostatic action:
if the diameter of the bacteriostatic ring is larger than 7mm, the bacteriostatic ring is judged to have bacteriostatic action.
If the diameter of the antibacterial ring is less than or equal to 7mm, the product is judged to have no antibacterial effect.
And 3 times of repeated tests show that the product has the bacteriostatic effect, and the product is judged to be qualified.
The negative control group should have no bacteriostatic ring. Otherwise the test is invalid.
The results are shown in Table 4.
TABLE 4
Figure BDA0002341337050000221
The results show that all the examples have bacteriostatic effect, and the bacteriostatic ring is larger than 7 mm. However, the ideal bacteriostatic ring in the application needs to be more than or equal to 40mm to meet the invention requirement, so the bacteriostatic effect of the examples 1,2, 3, 4, 5 and 6 is qualified, but the requirement of the application cannot be met.
Test example 4: instant bacteriostatic ATP instrument detection
Detecting a sample: fabric cleaning compositions and Cleaner Water of examples 1-4
The detection method comprises the following steps:
a2-wheat suspension of M.ostreatus (M.oslorensis, ATCC19976) was prepared in a turbidimetric tube (M.oslorensis, N.oslorens, N.oslera) (10 ≈ 10)8cfu/mL)。
The sterilized cloth pieces were soaked in a bacterial suspension of 2 wheat of Moraxella oselta (M.oslorensis, ATCC19976) for 5s and placed in an oven at 37 ℃ for 4 h.
A laundry detergent group: one of the cloth sheets is evenly coated with 0.8g or 2.0g of detection sample for 5 min.
Clear water control group: 2.0mL of sterilized standard hard water was added to the cloth and allowed to act for 5 min.
Putting the cloth pieces together with the laundry detergent/hard water into a 1L beaker filled with 400mL of standard hard water, adjusting the rotating speed of a magnetic stirrer to 2 grades, stirring for 15min at room temperature (washing), then transferring the cloth pieces into another 1L beaker filled with 400mL of standard hard water, stirring for 5min at the rotating speed of 2 grades at room temperature (rinsing), and finally transferring the cloth pieces into another 1L beaker filled with 400mL of standard hard water, stirring for 5min at the rotating speed of 2 grades at room temperature (rinsing).
The cloth pieces were placed in 10mL sterile PBS, shaken for 1min, and the appropriate dilution was taken to the CelisisPCP Advance microbial Rapid test Instrument for testing. The results are shown in Table 5.
TABLE 5
Log RLU Example 1 Example 2 Example 3 Example 4 Clean water
0.8g laundry detergent 3.53 3.19 3.42 3.26 5.22
2.0g laundry detergent 2.4 2.38 2.62 2.46 5.19
The results show that the examples 1,2, 3 and 4 have obvious instant bacteriostatic effect compared with the clear water, the instant bacteriostatic effect is considered to be the instant bacteriostatic effect when the Log RLU value is less than 4 according to the Log RLU values of the examples 1 to 4 and the clear water, and the instant bacteriostatic effect of the examples 1,2, 3 and 4 is almost the same from the data point of view, and the effect of the example 2 is the best.
Test example 5: delayed bacteriostatic ATP instrument detection
Detecting a sample: examples 1-4 Fabric cleaning compositions and Cleaner Water
The detection method comprises the following steps:
a laundry detergent group: one of the cloth sheets is evenly coated with 0.8g or 2.0g of detection sample for 5 min.
Clear water control group: 2.0mL of sterilized standard hard water was added to the cloth and allowed to act for 5 min.
Putting the cloth pieces together with the laundry detergent/hard water into a 1L beaker filled with 400mL of standard hard water, adjusting the rotating speed of a magnetic stirrer to 2 grades, stirring for 15min at room temperature (washing), then transferring the cloth pieces into another 1L beaker filled with 400mL of standard hard water, stirring for 5min at the rotating speed of 2 grades at room temperature (rinsing), and finally transferring the cloth pieces into another 1L beaker filled with 400mL of standard hard water, stirring for 5min at the rotating speed of 2 grades at room temperature (rinsing).
And putting the cloth piece into a 37 ℃ oven for placing until the cloth piece is completely dried.
A2-wheat suspension of M.ostreatus (M.oslorensis, ATCC19976) was prepared in a turbidimetric tube (M.oslorensis, N.oslorens, N.oslera) (10 ≈ 10)8cfu/mL) and gradually diluted to 105cfu/mL。
Adding 10 of 500 mu L into each piece of cloth5cfu/mL of a bacterial suspension of Moraxella osendani (M.oslorensis, ATCC19976) and cultured at 37 ℃ with a humidity of 80% for 24 hours.
The cloth pieces were placed in 10mL sterile PBS, shaken for 1min, and the appropriate dilution was taken to the CelisisPCP Advance microbial Rapid test Instrument for testing. The results are shown in Table 6.
TABLE 6
Log RLU Example 1 Example 2 Example 3 Example 4 Clean water
0.8g laundry detergent 2.63 2.59 2.44 2.88 3.14
2.0g laundry detergent 2.68 2.61 2.59 2.6 3.21
The results show that the examples 1,2, 3 and 4 have obvious time-delay bacteriostatic effects compared with the clear water, and according to the Log RLU values of the examples 1 to 4 and the clear water, the early judgment that the Log RLU value is less than 3 is considered to have the time-delay bacteriostatic effect, and the time-delay bacteriostatic effects of the examples 1,2, 3 and 4 are almost the same from the data point of view.
Example 18: preparation of Fabric cleaning compositions
Firstly, 0.06 mass part of dichloro-ethylene is dissolved in 6 mass parts of polyoxyethylene fatty alcohol ether to prepare small materials. Weighing 60 parts by mass of deionized water, placing the deionized water in a beaker, sequentially adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine under the stirring state at the rotating speed of 400rpm, and stirring until the mixture is clear and transparent. Then adding 5 parts by mass of disodium ethylene diamine tetraacetate, 0.2 part by mass of Medley SmartR100L enzyme, 0.5 part by mass of essence P15P822 ISLAND and 0.05 part by mass of essence POWER POPSCENTP52G708, and stirring until the mixture is clear and transparent for later use.
Example 19: preparation of Fabric cleaning compositions
Firstly, 0.06 mass part of triclosan bactericide is dissolved in 6 mass parts of polyoxyethylene fatty alcohol ether to prepare small materials. Weighing 60 parts by mass of deionized water, placing the deionized water in a beaker, sequentially adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine under the stirring state at the rotating speed of 400rpm, and stirring until the mixture is clear and transparent. Then adding 5 parts by mass of disodium ethylene diamine tetraacetate, 0.2 part by mass of MedleySmartR 100L enzyme, 0.05 part by mass of essence POWERFUL POPSCENT P52G708 and 0.5 part by mass of essence FRESHDEW P95L369, and stirring until the mixture is clear and transparent for later use.
Example 20: preparation of Fabric cleaning compositions
Firstly, 0.06 mass part of triclosan bactericide is dissolved in 6 mass parts of polyoxyethylene fatty alcohol ether to prepare small materials. Weighing 60 parts by mass of deionized water, placing the deionized water in a beaker, sequentially adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine under the stirring state at the rotating speed of 400rpm, and stirring until the mixture is clear and transparent. Then adding 5 parts by mass of disodium ethylene diamine tetraacetate, 0.2 part by mass of MedleySmartR 100L enzyme, 0.5 part by mass of essence P15P822 ISLAND, 0.05 part by mass of essence POWERFUPPOSCENT P52G708 and 1 part by mass of plant odor removing agent TH-70, and stirring until the mixture is clear and transparent for later use.
Example 21: preparation of Fabric cleaning compositions
Firstly, 0.06 mass part of triclosan bactericide is dissolved in 6 mass parts of polyoxyethylene fatty alcohol ether to prepare small materials. Weighing 60 parts by mass of deionized water, placing the deionized water in a beaker, sequentially adding 10 parts by mass of sodium fatty alcohol-polyoxyethylene ether sulfate, the small materials, 4 parts by mass of sodium dodecyl benzene sulfonate and 3 parts by mass of cocamidopropyl hydroxysultaine under the stirring state at the rotating speed of 400rpm, and stirring until the mixture is clear and transparent. Then adding 5 parts by mass of disodium ethylene diamine tetraacetate, 0.2 part by mass of MedleySmartR 100L enzyme, 0.5 part by mass of essence P15P822 ISLAND, 0.05 part by mass of essence POWERFUPPOSCENT P52G708 and 2 parts by mass of plant odor-removing agent AIRKEM198, and stirring until the mixture is clear and transparent for later use.
Table 7 summarizes the plant flavor and fragrance used in examples 18-21.
TABLE 7
Figure BDA0002341337050000251
Figure BDA0002341337050000261
Test example 6: odor removal test
Detecting a sample: fabric cleaning compositions of examples 18-19 and commercial product, Suzuo Sun Demy mildew laundry detergent
The detection method comprises the following steps:
preparation of a mould flavour mimic
The musty simulant was purchased from Fenmeiyi. Preparing a required amount of the mould simulant before each test; to ensure the accuracy of the experiment, the simulants used in the test were prepared from the same batch of starting materials within 1 hour prior to testing.
Preparation of reference samples
Taking a piece of towel for testing, soaking and rubbing for 10 times in a basin, and wringing; 0.02 g of mold simulant (0.04 g in total) was dropped on each of the front and back sides of the towel.
Preparation of test samples
2L of water is put into a basin, 5g of test sample is added, and the test sample is stirred by hand to be completely dissolved; putting a piece of towel for testing to soak, rubbing and washing the front and back surfaces of the towel for 10 times respectively, and soaking for 10 minutes; rinsing with 4 liters of water, rubbing and washing the front and back sides for 10 times respectively, and wringing; 0.02 g of mold simulant (0.04 g in total) was dropped on each of the front and back sides of the towel.
Odor evaluation-Wet towel
And smelling the moldy reference sample, sequentially evaluating the test samples, and grading according to requirements, wherein the grade is used as a wet and smelling evaluation result.
Odor evaluation-Dry towel
The wet towel was air dried, and 0.02 g of mold simulant (total 0.04 g) was dropped on both sides, and the samples were evaluated sequentially, and then, after rubbing, the evaluation was performed again, which is the dry-smelling evaluation result.
Reference table for mould and flavour scores:
Figure BDA0002341337050000271
the result of the detection
The test samples were taken, the towels were washed according to the standard washing method described above, and then the musty odor masking effect in the wet and dry towel states was evaluated, with the results shown in tables 8 to 9.
TABLE 8
Wet towel Example 18 Example 19 Commercial products
Intensity of musty taste 0.8 0.8 1.3
Intensity of fragrance 4.5 4.4 3.7
A commercial product is an aomiao sun de-musty laundry detergent.
TABLE 9
Dry towel Example 18 Example 19 Commercial products
Intensity of musty-before rubbing 2.4 2.2 3.0
Intensity of musty-after rubbing 0.7 0.8 3.0
Fragrance intensity-before rubbing 2.8 2.6 2.2
Fragrance intensity-after rubbing 4.2 4.0 2.2
A commercial product is an aomiao sun de-musty laundry detergent.
As can be seen from the results, examples 18 and 19 have stronger fragrance retention and a better covering effect on musty odor in the wet towel state; in the dry towel state, when not rubbed, the fragrance retention of all samples was reduced due to the emission during the day, but in comparison, the fragrance retention of examples 18 and 19 was still slightly better, and after rubbing, the stronger and better fragrance expression was brought due to the rupture release of the microcapsule essence, and the musty odor was basically not smelled; that is, examples 18 and 19 showed better mold masking than the reference commercial product in both wet and dry towel states.
Test example 7: odor removal test
Detecting a sample: fabric cleaning compositions of examples 18, 20, 21
The detection method comprises the following steps:
0.2 grams of a mold simulant (5 times normal dose, severe mold) was dropped on both sides of the test towel, and the test sample was then used to clean the towel according to the standard method described above.
In the towel soaking stage in water, the musty smell in the towel of the example 18 is reduced greatly, and the towel can smell a little musty smell; the musty was also much reduced in the example 20 towel and a bit of musty was likewise noticed, but less musty than the example 18 towel; no musty odor was noted in the example 21 towels. At this stage, example 21 had the best mold odor removing ability, followed by example 20 and example 18. In the towel wringing stage, no musty smell is smelled on the towels of examples 18, 20 and 21. The combination of the above two stages provides example 21 with the best mold removal.
Test example 8: detergency test
Detecting a sample: examples 18, 20 and 21, commercial products of the liquid laundry detergent for removing musty smell by using good sunlight
The detection method comprises the following steps: the detergency is tested by referring to the standard of GBT 13174-2008 determination of detergency and cyclic washing performance for dress materials.
Hard water preparation:
250mg/kg (as CaCO) is adopted for preparing the detergent solution in the washing experiment3Denoted, the same below) hard water, Ca2+With Mg2+The molar ratio is 6:4, and the preparation method comprises the following steps: 16.70g of calcium chloride and 20.37g of magnesium chloride are weighed to prepare 10.0L of hard water, namely 1500mg/kg of hard water. When in use, 1.0L of the water is taken to be flushed to 10.0L, namely 250mg/kg of hard water.
Measurement of whiteness:
the whiteness measurement should be carried out as follows:
according to the requirements of detergent performance test, selecting the required JB series test piece variety. Cutting the dirty cloth for measurement into test pieces, respectively matching six groups with similar average blackness according to categories, if the test pieces are JB-00, 6 test pieces should be in each group, and if the test pieces are other JB types, at least 4 test pieces should be in other JB types, and simultaneously making numbering records, wherein each group of test pieces is used for the performance test of one sample.
Test pieces were stacked in a uniform manner, and the whiteness values before and after washing were intentionally read at 457nm with a whiteness meter. Measuring the whiteness value by using two song points on the front and back surfaces of the test piece (the bright points on each surface are centrosymmetric), and taking the average value of four measurements as the before-washing whiteness F1 of the test piece; the whiteness of the test piece after washing was measured at two points on each of the front and back surfaces (the two points on each surface should be centrosymmetric), and the average of the four measurements was defined as the whiteness of the test piece after washing F2.
In order to ensure the reliability of the comparative experiment results, the quantity and the variety of each group of test pieces are the same during the decontamination washing determination. When the detergency of the detergent is tested separately for different stains, each group of test pieces has at least 6 pieces. When the detergency is tested on a plurality of dirty cloths together, each dirty cloth has at least 3 pieces of test pieces, and the number of each set of test pieces is controlled within 8-12 pieces.
The washing experiment is carried out in a vertical decontamination machine, the stirring impellers, the working tank and the decontamination bathtub are numbered and fixed one by one to form a working unit before measurement, and the instrument is preheated to 30 +/-1 ℃ for a period of time. In the test, 250mg/kg of hard water (used when the test is preheated to about 30 ℃) is used for respectively preparing a test solution 1L with a certain concentration (when not particularly stated, the concentration of the standard laundry detergent and the concentration of the test solution are both not 0.2%) by using a sample and a standard laundry detergent, the test solution is poured into a corresponding decontamination bathtub, the corresponding position of the decontamination bathtub is placed, a stirring impeller is installed, and the instrument is adjusted to keep the temperature of the washing test at 30 +/-1 ℃ for the preparation of the test.
1mL of reference protease solution with a certain concentration can be added into the standard laundry detergent solution in the decontamination bathtub according to the test requirements of the sample, and the stirring is started for 30s and then stopped.
Putting the test pieces of each group for measuring whiteness into a bathtub respectively, starting stirring, keeping the stirring speed at 120r/min (angular speed of 220 pi/min), and stopping the washing process after the washing process lasts for 20 min.
Combining the test pieces in each decontamination bathtub, pouring the test pieces into an inner barrel of a rinsing device, draining the water, putting the test pieces into the rinsing device, pouring 1500mL of tap water, covering a cover, rotating an upper handle of the rod to enable the inner barrel to rotate for about 30s and then stop (the inner barrel needs to be fully rotated in the period, but the overflow of rinsing water in a container needs to be avoided due to the fact that the inner barrel rotates too fast). The rinsed water was drained off, 1500mL of tap water was added again, and the second rinsing was repeated. The rinsing water was drained off and the test pieces were dehydrated manually for 15s (rotation speed about 1800 r/min). And taking out the rinsed test piece, hanging the test piece at room temperature, and airing to measure the whiteness F2.
And calculating the whiteness difference (F2-F1) of each test piece before and after washing in a one-to-one correspondence manner, and respectively carrying out Q value detection on each group of test pieces under the condition that the confidence coefficient is 90 percent, and taking up or rejecting suspicious values. The data which is required to be discarded when each group of test pieces exceeds the limit range does not exceed one, otherwise, the group of tests is abandoned and the test needs to be repeated. After confirming the effective whiteness difference and the number n of test piecesThe detergency ratio (R) was calculated by the following formulai)。
Ri=Σ(F2i-Fu)/n
The results are shown in Table 10.
Watch 10
Example 18 Example 20 Example 21 Commercial products
Detergency 4.4 4.3 4.3 3.9
The commercial product is "wonderful sunshine mildew-off laundry detergent".
Examples 18, 20, 21 all had comparable and better detergency than the commercial products.
Test example 9: zone of inhibition detection
Detecting a sample: examples 18, 20 and 21, bacteriostatic effects of the Competition on Ousland Moraxella anserina ATCC19976
The detection method comprises the following steps:
preparing the bacteriostatic tablets:
for liquid bacteriostat, a sterile and dry filter paper sheet is taken. Dripping 20 μ l of bacteriostatic agent solution with practical use concentration into each piece, placing the filter paper piece in a clean sterile plate, opening the cover, and oven drying in a warm box (37 deg.C), or naturally drying at room temperature for use.
The dissoluble antibacterial product can be directly made into round pieces (blocks) with the diameter of 5mm and the thickness of not more than 4mm, and every 4 round pieces (blocks) are in a group.
And (3) preparing a negative control sample sheet, namely taking a sterile dry filter paper sheet, dropwise adding 20 mu l of sterile distilled water into each sheet, and drying for later use.
The negative control sample of the dissoluble antibacterial product is prepared by taking a sample which is made of the same material and does not contain the antibacterial component, and preparing a sample slice (block) with the same size as the test group.
Inoculation of test bacteria: dipping with sterile cotton swab to 5 × 10 concentration5cfu/ml~5×106cfu/ml test bacterial suspension was evenly spread on the surface of nutrient agar medium plate for 3 times. For each application 1 time, the plate should be rotated 60 °, and finally the cotton swab is applied around the edge of the plate for one revolution. The plate was covered and dried at room temperature for 5 min.
And (3) sticking bacteriostatic agent sample sheets, namely sticking 1 bacteriostatic flat plate on each test, sticking 4 test sample sheets and 1 negative control sample sheet on each flat plate, and sticking 5 negative control sample sheets. A sample was taken with sterile forceps and placed on the surface of the plate. The distance between the centers of the various pieces is more than 25mm, and the distance between the centers of the various pieces and the periphery of the flat plate is more than 15 mm. After the sample is placed, the sample is lightly pressed by using sterile tweezers to be tightly attached to the surface of the flat plate. The plate is covered, the plate is placed in an incubator at 37 ℃, and the result is observed after the plate is cultured for 16 to 18 hours. The diameter of the antibacterial ring (including the patch) was measured with a vernier caliper and recorded. The experiment was repeated 3 times.
When the inhibition zone is measured, the inhibition zone which is uniform and completely aseptically grows is selected for measurement. The diameter of the catheter is measured by taking the outer edge of the bacteriostatic ring as a boundary.
The evaluation rules are:
judging the bacteriostatic action:
if the diameter of the bacteriostatic ring is larger than 7mm, the bacteriostatic ring is judged to have bacteriostatic action.
If the diameter of the antibacterial ring is less than or equal to 7mm, the product is judged to have no antibacterial effect.
And 3 times of repeated tests show that the product has the bacteriostatic effect, and the product is judged to be qualified.
The negative control group should have no bacteriostatic ring. Otherwise the test is invalid.
The results are shown in Table 11.
TABLE 11
Example 18 Example 20 Example 21 Competition material
Zone of inhibition mm 41 41 41 25
Grade ++++ ++++ ++++ ++
The competitive product is 'wonderful sunshine mildew-free laundry detergent'.
The results show that the bacteriostatic effects of the examples 18, 20 and 21 are consistent and better than the bacteriostatic effect of competitive products.

Claims (10)

1. A cleaning composition for removing the shade-dried odor of fabrics comprising:
15-65% by weight of a surfactant;
0.01-2% by weight of a bactericide;
0.05-3 wt% of essence;
0.1-2 wt% of an enzyme;
1-10 wt% of a chelating agent; and
a carrier that is acceptable in the field of fabric cleaning,
wherein the surfactant is selected from: a non-ionic surfactant, an anionic surfactant, a zwitterionic surfactant, or a combination thereof,
wherein the enzyme is a mixture of protease, lipase and cellulase.
2. The cleaning composition of claim 1, further comprising an odor eliminator.
3. The cleaning composition of claim 2, wherein the odor eliminating agent is a plant odor eliminating agent in an amount of up to about 2 wt.%.
4. The cleaning composition of claim 1, wherein the surfactant is selected from the group consisting of: sodium fatty alcohol polyoxyethylene ether sulfate, polyoxyethylene fatty alcohol ether, sodium dodecyl benzene sulfonate, cocamidopropyl hydroxysultaine, fatty acid methyl ester ethoxylate or their combination.
5. The cleaning composition of claim 1, wherein the germicidal agent is selected from the group consisting of: triclosan, triclocarban, p-chloro-m-xylenol, or combinations thereof.
6. The cleaning composition of claim 1, wherein the perfume is selected from the group consisting of: free oil flavors, microencapsulated flavors, or a combination thereof.
7. The cleaning composition of claim 1, wherein the enzyme is present in the composition in an amount of about 0.2 wt.%, based on the total weight of the composition.
8. The cleaning composition of claim 1, further comprising an adjunct acceptable in the fabric cleaning art.
9. A method of removing the shade-dried odor of a fabric comprising contacting the fabric with an effective amount of the cleaning composition of claim 1.
10. The method of claim 9, wherein the contacting step is performed in a wash cycle of a manual wash or an automatic washing machine.
CN201911377302.XA 2019-12-27 2019-12-27 Cleaning composition for removing odor of fabrics dried in the shade Pending CN111117811A (en)

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CN112359596A (en) * 2020-10-28 2021-02-12 合肥艾尔纳新材料科技有限公司 Novel cloth deodorant and preparation method thereof
CN112538758A (en) * 2020-12-15 2021-03-23 上海家化联合股份有限公司 Fabric care compositions with softening, antistatic, and shade drying odor removal properties

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CN106350287A (en) * 2016-08-23 2017-01-25 余姚市德派日用品有限公司 Laundry gel beads for washing sportswear and preparation method of laundry gel beads
CN107012011A (en) * 2017-04-28 2017-08-04 明光市飞洲新材料有限公司 It is a kind of can be with washing powder of disinfecting mite-removing and preparation method thereof

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CN1094749A (en) * 1993-04-30 1994-11-09 刘永焰 A kind of washing composition that has sterilization, germicidal action concurrently
CN103468421A (en) * 2013-08-12 2013-12-25 广西和桂集团有限公司 Liquid laundry detergent and preparation technology thereof
CN103695201A (en) * 2013-11-28 2014-04-02 南通市通州区大达麻纺织有限公司 Disinfectant washing powder for fabric and preparation method thereof
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CN112359596A (en) * 2020-10-28 2021-02-12 合肥艾尔纳新材料科技有限公司 Novel cloth deodorant and preparation method thereof
CN112538758A (en) * 2020-12-15 2021-03-23 上海家化联合股份有限公司 Fabric care compositions with softening, antistatic, and shade drying odor removal properties

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