CN107898651A - A kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue and preparation method thereof - Google Patents

A kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue and preparation method thereof Download PDF

Info

Publication number
CN107898651A
CN107898651A CN201711094247.4A CN201711094247A CN107898651A CN 107898651 A CN107898651 A CN 107898651A CN 201711094247 A CN201711094247 A CN 201711094247A CN 107898651 A CN107898651 A CN 107898651A
Authority
CN
China
Prior art keywords
wet tissue
ammonium salt
quaternary ammonium
organosilicon
acrylamide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201711094247.4A
Other languages
Chinese (zh)
Inventor
葛宏伟
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.)
SUZHOU BORAGE DAILY CHEMICAL CO Ltd
Original Assignee
SUZHOU BORAGE DAILY CHEMICAL CO Ltd
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 SUZHOU BORAGE DAILY CHEMICAL CO Ltd filed Critical SUZHOU BORAGE DAILY CHEMICAL CO Ltd
Priority to CN201711094247.4A priority Critical patent/CN107898651A/en
Publication of CN107898651A publication Critical patent/CN107898651A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0208Tissues; Wipes; Patches
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/347Phenols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35Ketones, e.g. benzophenone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35Ketones, e.g. benzophenone
    • A61K8/355Quinones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds
    • A61K8/553Phospholipids, e.g. lecithin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/604Alkylpolyglycosides; Derivatives thereof, e.g. esters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/67Vitamins
    • A61K8/678Tocopherol, i.e. vitamin E
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/68Sphingolipids, e.g. ceramides, cerebrosides, gangliosides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/005Antimicrobial preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/005Preparations for sensitive skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M14/00Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials
    • D06M14/18Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation
    • D06M14/20Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation on to materials of natural origin
    • D06M14/22Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation on to materials of natural origin of vegetal origin, e.g. cellulose or derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/52Stabilizers
    • A61K2800/524Preservatives

Abstract

A kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue, it includes wet tissue body and wet tissue liquid, wherein, wet tissue body is the non-woven fabrics for being bonded high molecular quaternary;Wet tissue liquid selective RO purified waters, 12 18 alkyl glucosides, lecithin or hydrolecithin, 1,2 pentanediols, skin conditioning agent, other additives, then the ozone concentration of 0.1 1.0mg/L is passed through in wet tissue liquid, finally, wet tissue liquid is added to wet tissue body by certain weight ratio, pack, that is, form a kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue.The product belongs to the wet tissue of zero precipitation preservative, soft to skin, non-stimulated, without allergy, especially suitable for allergy skin, the tender skin of children etc..

Description

A kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue and preparation method thereof
Technical field
The present invention relates to a kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue, more particularly to a kind of infant Hip pad wet tissue.
Background technology
In recent years, since the application of wet tissue brings convenience to the life of people, it is increasingly becoming in people's life Necessity, therefore the annual output of wet tissue and consumption rapid growth, along with the application field of wet tissue constantly expands, corresponding production The exploitation of product requires also higher and higher.At present, wet tissue species is relatively more, there is hand mouth wet tissue, wet sanitary napkins, makeup-removing wet tissue, clean skin Wet tissue etc., with the lasting expansion of market scale, national industrial policies encourage wet tissue industry to high-tech, high value added product Direction is developed, and improves product competitiveness and the market share, therefore the exploitation of wet tissue formula technique will play an important role.
Wet tissue preservative is the topic that consumer especially pays close attention to, and most preservative be all by with cell membrane contact Afterwards, with some components of cell membrane, mainly with albumen qualitative response, the protection structure or interference cell of microbial cell are destroyed Metabolism, influences the normal growth order of cell, so as to reach corrosion-resistant purpose, cation is then mainly oozed by influencing it Pressure thoroughly, makes membranolysis, contraction and dehydration, so as to be sterilized.Mainly there are 3 kinds of modes:1) make microprotein be denatured or Solidification, there is substantial amounts of protein in microbial body, all factors that can destroy protein spatial configuration, can make protein denaturation or Solidification.2) enzyme system of microorganism is disturbed, the effect of microorganism endocellular enzyme is related with its active group, all to change or destroy born of the same parents The material of interior enzymatic activity group function, can suppress the activity of microbial enzyme.3) membrane passage, cationic surface are changed After activating agent and phenols act on microorganism, membrane structure can be changed, disturb its normal function, so it is dead.
Preservative species used in China's wet tissue industry is various at present, wherein the overwhelming majority is chemical preservative, chemistry Preservative is because its is simple in structure, the mechanism of action is apparent, property is stable, has a broad antifungal spectrum, cheap and deep liked by wet tissue producer Love.In fact, some people have found mysterious phenomenon in the user of preservative, the addition of same preservative is It is several times several years ago, the putrid and deteriorated phenomenon of product still occurs, most of is because certain a kind of (kind) sterilization antiseptic length Phase is used continuously and causes flora to reduce the sensitiveness of the fungicide, so as to cause antisepsis and sterilization effect to decline, here it is institute The microorganism of meaning in this case also easily causes consumer skin the feelings such as allergy, stimulation to the resistance to the action of a drug of sterilization antiseptic Condition.But the continuous improvement and the growing interest to health, people realized with the reach of science, consumer safety are gradually sent out Chemical preservative in existing wet tissue can produce ill-effect to human body, therefore the requirement that wet tissue preservative uses is also higher and higher, Wet tissue industry is promoted to begin look for the alternative route of chemical preservative, to reduce the injury to consumer skin.And traditional change " green ", " health " idea that preservative has been unable to meet people's pursuit are learned, and the appearance of natural antiseptic agent and preservative free is proper It compensate for this part vacancy well, therefore study and have become mesh using non-stimulated, safe chemical preservative substitute A kind of trend in preceding daily use chemicals industry.
CN103566371A discloses a kind of antimicrobial method, it is by the organosilicon bi-quaternary ammonium salt of lower formula (I): (R1R2R3N+X-) wherein, each R1 independently is C8-18 alkyl, C8-18 alkenyls or C8-18 to-R5- (R1R2R3N+X-) (I) Alkynyl;Each R2 and R3 independently is methyl or ethyl;R5 is C3-10 alkylidenes, it is in β-position or more distant positions by three (C1- 3 alkoxies) siloxy or three (C1-3 alkoxies) silicyl-C1-6 alkoxies substitution;Independently being with each X- can Acceptable counter anion, being applied to needs to form antimicrobial membranes on antimicrobial body surface.The physics antimicrobial membranes, The mould proof of every profession and trade, antibacterial, deodorization are can be widely used for, also can combine to form new combination articles, example with the product of these industries Such as paper industry, face tissue, hygenic towelette, dixie cup etc..But the wet tissue obtained with this method still has the problem of separating out preservative, resist Bacterium performance need to be improved, and comfort also has much room for improvement.
CN101716359A discloses a kind of bactericidal disinfectant material, it is will to carry capture bacterium, disease by graft process The compound of functional group of poison is fixed on nonwoven fabric surface with chemical bond, which includes quaternary ammonium salt, sulfur-containing compound, Containing the one or more in sulfoacid compound.The bactericidal disinfectant material can be widely used in sterilizing product, such as wet Towel, cotton balls, disinfection infantees etc..
CN106726636A discloses a kind of physical antibacterial wet tissue, and bi-quaternary ammonium salt is grafted on wet tissue by it by x ray irradiation x On body, antibiotic property, soft and smooth property and the less antibacterial wet tissue of irritation have been obtained.But the grafting of above-mentioned graft reaction Rate, and the wet tissue need further to be lifted in antibiotic property, flexibility, smoothness and irritation.
In order to solve the problems, such as wet tissue antibiotic property, flexibility, smoothness difference in the prior art and there is irritating, this hair Bright to provide a kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue, its effect is by positively charged anti-micro- life Thing film or particle produce electrostatic force with negatively charged microbial cell film and make it that microbial cell film ruptures or form changes Become and cause microorganism dead, so as to be provided with anti-corrosive antibacterial ability, the product strong antibacterial, flexibility and smoothness are good, It is soft to skin, non-stimulated, without allergy, especially suitable for allergy skin, the tender skin of children etc..
The content of the invention
The present invention provides a kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue.The wet tissue includes wet tissue sheet Body and wet tissue liquid, wet tissue body have selected with antimicrobial membranes or the non-woven fabrics of nano particle with positive charge, this is anti- Microbial film or nano particle are formed by chemical bonds;Wet tissue liquid selective RO purified waters, 12-18 alkyl glucosides Glycosides, lecithin or hydrolecithin, 1,2- pentanediols, skin conditioning agent, other additives, are then passed through in wet tissue liquid The ozone concentration of 0.1-1.0mg/L, finally, is added to wet tissue body by certain weight ratio by wet tissue liquid, packs, i.e. shape Into a kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue.
Specifically, the present invention provides a kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue, it is by wet tissue Body and wet tissue liquid composition, the wet tissue body is the non-woven fabrics for being bonded high molecular quaternary;The wet tissue liquid be by It is following to be formed with each component of percentage by weight:
RO purified waters 65-70%
12-18 alkyl glucosides 0.1-0.6%
Lecithin or hydrolecithin 0.2-0.5%
1,2- pentanediol 25-30%
Skin conditioning agent 0.2-2%
Other additives 1-6%,
The sum of each component content is 100%.
Wherein, the preparation method of wet tissue body is:
(1) length is used as 40-50mm, and the bamboo pulp fiber of a diameter of 0.04-0.1mm is as raw material, through cross lapping water Bamboo pulp non-woven fabrics is made after piercing technique, the nonwoven carrier that thickness is 3-5mm is obtained after clipped, high-temperature sterilization;
(2) nonwoven carrier made from step (1) is placed in the monomer solution of isopropanol/water mixed solvent preparation, room When the lower lucifuge immersion 12-24 of temperature is small;
(3) under nitrogen protection, CeCl is added in monomer solution3/ HCl/water solution, with x ray irradiation x above-mentioned steps (2) In it is soaking after obtained non-woven fabrics, irradiation intensity 80-200KGy;
(4) after irradiating, unreacted monomer and homopolymer are fallen in extracting, and wet tissue body is obtained after dry;
Wherein, monomer is organosilicon bi-quaternary ammonium salt and acrylamide, the quality point of organosilicon bi-quaternary ammonium salt in monomer solution Number is 0.2-0.3%, and the molar ratio of organosilicon bi-quaternary ammonium salt and acrylamide is (10-20): 1;CeCl3In the reaction system Initial concentration be (1-2) × 10-4The initial concentration of mol/L, HCl in the reaction system is (1-2) × 10-3mol/L;
The organosilicon bi-quaternary ammonium salt is the compound shown in formula 1 or formula 2:
The ray is selected from ultraviolet, electron beam, X-ray, alpha ray, β rays or gamma-rays;
The skin conditioning agent is ceramide, one kind in Co-Q10, tocopherol acetate, resveratrol, astaxanthin It is or a variety of.
Other described additives are antioxidant, one or more kinds of mixtures in chelating agent, pH adjusting agent, It is chosen in particular from one or more kinds of in Butylated Hydroxytoluene, EDTA-2Na, EDTA-4Na, arginine, citric acid, sodium citrate Mixture.
The 12-18 alkyl glucosides are lauryl glucoside or octadecyl glucoside.
Present invention also offers a kind of preparation method of wet tissue liquid, it is characterised in that wet tissue liquid is the shield of transparent and stable Skin lotion, this method comprises the following steps:
(1) 12-18 alkyl glucosides 0.1-0.6%, lecithin or hydrolecithin 0.2-0.5% are mixed and heated To 50-80 DEG C, at this temperature, 5-20min is quickly stirred, to obtaining clear solution A;
(2) RO purified waters 65-70%, 1,2- pentanediols 25-30%, other additives 1-6% are mixed and heated to 60- 90 DEG C, it is evenly stirred until clear solution B;
(3) under high-speed stirred, B solution is slowly added in solution A, until obtaining clear solution C;
(4) C solution that cools down adds skin conditioning agent 0.2-2%, stirs evenly and clear solution D is made to less than 45 DEG C;
(5) ozone is passed through in solution D, ozone concentration is maintained in the range of 0.1-1.0mg/L, up to wet tissue liquid E.
Further, present invention also offers a kind of preparation of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue Method, it is characterised in that add the ratio of wet tissue liquid E and the wet tissue body by weight 1.5: 1-4: 1 for being cut into suitable dimension Add, then pack, up to acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue.
The acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue of the present invention has the work killed or suppress microorganism With its is safe to the human body, and can be produced to avoid drug resistance caused by chemical antibiotic antiseptic., should compared with traditional wet tissue Wet tissue has the following advantages that:
1st, traditional wet tissue is that antiseptic is fixed in non-woven fabrics using adhesive, and the wet tissue is by stable chemistry Bond is the product of zero precipitation preservative together in non-woven fabrics;
2nd, traditional wet tissue anti-corrosion function is protection structure or the metabolism of interference cell by destroying microbial cell, The normal growth order of cell is influenced, so as to reach corrosion-resistant purpose.And the wet tissue anti-corrosion function is resisted by positively charged Microbial film or nano particle make the rupture of microbial cell film dead with negatively charged microbial film by electrostatic force, from And reach anti-corrosive antibacterial function.
4th, chemical preservation antiseptic wet tissue imposes on human body surface for a long time may cause the symptoms such as human allergy, make as excessive With may result in dermatitis, spot, or even DNA damage can be caused.In addition, during production, variation bacterium or tolerance are also easily grown Bacterium, unpredictable security risk problem is added for company, and the application of the wet tissue completely avoid above-mentioned unfavorable factor.
5th, by CeCl3Make specific organosilicon bi-quaternary ammonium salt and acrylamide graft under/HCl initiation systems in wet tissue On body, the grafting rate of organosilicon bi-quaternary ammonium salt is improved, only excellent antibacterial effect is can reach with seldom amount of monomer, makes The antibacterial effect of the wet tissue has exceeded common antibacterial wet tissue of the prior art, and wet tissue has splendid flexibility and smooth Property, uses extremely gentle and nonirritant, drug resistance will not be produced, available for infant's hip pad wet tissue, infant's hand mouth Wet tissue, clean skin wet tissue and wet sanitary napkins etc., the wet tissue can be rapidly to skin problems such as dermatitis, eczema, bedsore, the red hip of baby Act, there is bacterio static itching-relieving, the positive effect of skin care, be particularly suitable for using during the red hip of baby.
Brief description of the drawings
Fig. 1 is the nuclear magnetic spectrogram of organosilicon bi-quaternary ammonium salt A described in preparation example 1.
Fig. 2 is the nuclear magnetic spectrogram of organosilicon bi-quaternary ammonium salt B described in preparation example 2.
Embodiment
Preparation example 1:
1) dry hydrogen chloride gas is imported in the anhydrous ether solution of octadecyldimethyl tertiary amine, it is heavy produces white Form sediment.Then using water as solvent, epoxychloropropane is placed in dropping funel, starts to be slowly added dropwise, 35min is dripped off, and is stirred at room temperature After mixing uniformly, 12h is reacted in 80 DEG C, reaction end is determined by titrating epoxychloropropane quaternary ammonium salt content, after completion of the reaction, Rotary evaporation removes solvent at room temperature, faint yellow paste residue is obtained, with acetone recrystallization paste residue, crystal to be separated out Decompression filters afterwards, is so repeated several times, and finally obtains white powder mono-quaternaries product --- intermediate product N- (the chloro- 2- hydroxypropyls of 3- Base)-N, N- dimethyl stearyl ammonium chlorides.Wherein, octadecyldimethyl tertiary amine: hydrogen chloride: mole of epoxychloropropane Than for 1.5: 1.2: 1.
2) N, N- dimethyl -1,2- are sequentially added in the four-hole boiling flask equipped with electric mixer, thermometer and still Ethylenediamine, methyl oleate, dibutyl tin dilaurate, hydroquinone, are warming up to 110 DEG C, when back flow reaction 4 is small.Then will be anti- Answer device to be changed to distilling apparatus, continue to stir, be distilled off at the reaction temperatures unreacted methyl oleate and its with methanol Azeotropic mixture.Stop reaction, vacuum distillation, vacuum drying obtain oleoyl ethyldimethyl amine.Wherein, N, N- dimethyl -1,2- second The molar ratio of diamines and methyl oleate is 1: 4, and dibutyl tin dilaurate, the dosage of hydroquinone are respectively reaction solution gross mass 2% and 0.1%.
3) products therefrom in step 1) is sequentially added in the four-hole boiling flask equipped with electric mixer, thermometer and still I, acetone, hydroquinone.Heating water bath adds step 2) products therefrom II, when reaction 4 is small to 60 DEG C.Filter and remove solvent, not The raw material and hydroquinone of reaction, crystallisation by cooling, filters to obtain product III.With acetone recrystallization 3-4 times, vacuum drying.Wherein, The molar ratio of product I and II are 1: 4, the dosage of hydroquinone, are the 0.15% of reaction solution gross mass
4) by products therefrom III in step 3) and γ-chloropropyl pi-allyl diethoxy silane under the conditions of being stirred at reflux 60 DEG C are warming up to, reacts 24h, vacuum distillation removes residue, then the dry 24h of 40 DEG C of vacuum, up to organosilicon bi-quaternary ammonium salt A。
Preparation example 2:
It is identical with preparation example 1, differ only in:The anhydrous ether of Dodecyl Dimethyl Amine is used in the 1) step Solution, finally obtains organosilicon bi-quaternary ammonium salt B.
Embodiment 1
The preparation method of wet tissue body is:
(1) length is used as 45mm, and the bamboo pulp fiber of a diameter of 0.07mm is as raw material, after cross lapping water jet process Bamboo pulp non-woven fabrics is made, the nonwoven carrier that thickness is 4mm is obtained after clipped, high-temperature sterilization;
(2) nonwoven carrier made from step (1) is placed in the monomer solution of 1L isopropanol/waters mixed solvent configuration, When lucifuge immersion 18 is small at room temperature, wherein monomer is organosilicon bi-quaternary ammonium salt A and acrylamide, organosilicon bi-quaternary ammonium salt in solution The mass fraction of A is 0.2%, and the molar ratio of organosilicon bi-quaternary ammonium salt A and acrylamide is 15: 1, the volume of isopropanol and water Than for 3: 1;
(3) under nitrogen protection, CeCl is added in monomer solution3/ HCl/water solution, with gamma-ray irradiation above-mentioned steps (2) in it is soaking after obtained non-woven fabrics, irradiation intensity 90KGy;CeCl3Initial concentration in the reaction system is 2 × 10-4The initial concentration of mol/L, HCl in the reaction system is 1 × 10-3mol/L;
(4) after irradiating, unreacted monomer and homopolymer are fallen in extracting, and wet tissue body is obtained after dry;
In the preparation process of wet tissue liquid E, solution A selects lauryl glucoside 0.1g, lecithin 0.5g.Solution B is selected 1,2- pentanediol 25g, EDTA-2Na 6g, RO purified water 66.4g.Skin conditioning agent selects water-soluble Cer NS g.
Specially:
1) lauryl glucoside 0.1g, lecithin 0.5g are mixed and heated to 60 DEG C, at this temperature, quickly stirred 15min, to obtaining clear solution A.
2) 1,2- pentanediols 25g, EDTA-2Na 6g, RO purified water 66.4g is mixed and heated to 70 DEG C, stirred evenly To clear solution B.
3) under high-speed stirred, B solution is slowly added in solution A, until clear solution C is obtained,
4) C solution that cools down adds water-soluble Cer NS g, stirs evenly and clear solution D is made to 40 DEG C.
5) ozone is passed through in solution D, ozone concentration is maintained at 0.3mg/L, up to wet tissue liquid E.
The ratio of above-mentioned wet tissue liquid E and wet tissue body by weight 4: 1 is added, is then packed, up to acryloyl Amine organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue.
Embodiment 2
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except organosilicon bi-quaternary ammonium salt A is replaced with organosilicon bi-quaternary ammonium salt B.
Embodiment 3
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except the mass fraction of organosilicon bi-quaternary ammonium salt A is replaced with 0.3%.
Embodiment 4
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except the mass fraction of organosilicon bi-quaternary ammonium salt A is replaced with 0.25%.
Embodiment 5
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except the molar ratio of organosilicon bi-quaternary ammonium salt A and acrylamide are replaced with 10: 1.
Embodiment 6
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except the molar ratio of organosilicon bi-quaternary ammonium salt A and acrylamide are replaced with 20: 1.
Embodiment 7
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except gamma-rays is replaced with ultraviolet.
Embodiment 8
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except by soaking time replace with 12 it is small when, irradiation intensity replaces with 200KGy.
Embodiment 9
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 2 is identical, and except lauryl glucoside is replaced with octadecyl glucoside, lecithin replaces with hydrolecithin.
Embodiment 10
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 2 is identical, except ozone concentration is maintained at 1.0mg/L.
Embodiment 11
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except the ratio of wet tissue liquid E and wet tissue body by weight 1.5: 1 is added.
Embodiment 12
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, and except the dosage of lauryl glucoside replaced with 0.6g, the dosage of lecithin replaces with 0.5g, and 1,2- penta The dosage of glycol replaces with 30g, and the dosage of EDTA-2Na replaces with 1g, RO purified waters 67.7g, the use of water-soluble ceramide Amount replaces with 0.2g.
Embodiment 13
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, and except the dosage of lauryl glucoside replaced with 0.3g, the dosage of lecithin replaces with 0.4g, and 1,2- penta The dosage of glycol replaces with 28g, and the dosage of EDTA-2Na replaces with 3g, RO purified waters 67.3g, the use of water-soluble ceramide Amount replaces with 1g.
Comparative example 1
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except the mass fraction of organosilicon bi-quaternary ammonium salt A is replaced with 0.1%.
Comparative example 2
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except monomer is only organosilicon bi-quaternary ammonium salt A.
Comparative example 3
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except being added without CeCl3/ HCl/water solution.
Comparative example 4
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except organosilicon bi-quaternary ammonium salt A is replaced with dimethyldiallylammonium salt.
Comparative example 5
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except organosilicon bi-quaternary ammonium salt A is replaced with N- methylacryoyloxyethyls-N, N- dimethylammonium-α-N- first Base carboxybetaine.
Comparative example 6
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except organosilicon bi-quaternary ammonium salt A is replaced with oleamide Ethyldimethylaminopropyl methyl dimethoxysilane Quaternary ammonium salt.
Comparative example 7
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except organosilicon bi-quaternary ammonium salt A is replaced with 2- triethoxysilicanes propane Oxy-1-octadecylene base-3- ten Eight alkyl dimethyl ammonium propane dichloride.
Comparative example 8
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except organosilicon bi-quaternary ammonium salt A is replaced with 2- triethoxysilicanes propane Oxy-1-octenyl-3- 18 Alkyl dimethyl ammonium propane dichloride.
Comparative example 9
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except organosilicon bi-quaternary ammonium salt A is replaced with 2- triethoxysilicanes propane Oxy-1-laurylene base-3- ten Eight alkyl dimethyl ammonium propane dichloride.
Comparative example 10
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except organosilicon bi-quaternary ammonium salt A is replaced with 2- triethoxysilicane propane Oxy-1-N, N- dimethyl allenes Acyl group -3- octadecyldimethyl ammonium propane dichloride.
Comparative example 11
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except organosilicon bi-quaternary ammonium salt A is replaced with 2- triethoxysilicane propane Oxy-1-N, N- dimethyl allenes Acyl group -3- dodecyl dimethyl ammonium propane dichloride.
Comparative example 12
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except monomer solution is replaced with 2- triethoxysilicane propane the Oxy-1s-N, N- that mass fraction is 0.2% The solution of Dimethylacryloyl -3- octadecyldimethyl ammonium propane dichloride.
Comparative example 13
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except monomer solution is replaced with 2- triethoxysilicane propane the Oxy-1s-N, N- that mass fraction is 0.2% The solution of Dimethylacryloyl -3- dodecyl dimethyl ammonium propane dichloride.
Comparative example 14
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except 1,2- pentanediols are replaced with 1,5-PD.
Comparative example 15
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except 1,2- pentanediols are replaced with 1,2-PD.
Comparative example 16
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, and except the dosage of 1,2- pentanediols is replaced with 22g, the dosage of RO purified waters replaces with 69.4g.
Comparative example 17
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, and except the dosage of 1,2- pentanediols is replaced with 33g, the dosage of RO purified waters replaces with 65g, EDTA-2Na Dosage replace with 1g, the dosage of water-soluble ceramide replaces with 0.4g.
Comparative example 18
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except lecithin is replaced with lanolin.
Comparative example 19
The preparation method of wet tissue body, wet tissue liquid E and acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue with Embodiment 1 is identical, except lauryl glucoside is replaced with sodium cocoyl glutamate.
Technique effect:
1. fungistatic effect
By the evaluation criterion testing example in Disposable Sanitary Accessory sanitary standard GB15979-2002 appendix Cs and The bacteriostasis rate of wet tissue, test result are as shown in table 1 in comparative example:
The fungistatic effect of 1 wet tissue of table
It can be seen from the data in table 1 compared with the wet tissue in comparative example, wet tissue product of the invention has more excellent Anti-microbial property.
2. soft and smooth property
Group is evaluated using 5 people to evaluate the soft and smooth property of wet tissue in embodiment and comparative example by ten point system, is surveyed Test result is as shown in table 2:
The soft and smooth property of 2 wet tissue of table
It can be seen from the data in table 2 compared with the wet tissue in comparative example, wet tissue product of the invention has more excellent Softness and smoothness.
3. irritation
Foundation《Disinfection technology standard》In an intact skin stimulation test to wet tissue carry out skin irritation detection, test The results are shown in Table 3:
The irritation of 3 wet tissue of table
Standards of grading:
Erythema is formed:0 is nothing, and 1 is, reluctantly as it can be seen that 2 be obvious, 3 is serious, and 4 be aubergine erythema, and has eschar;
Oedema is formed:0 is nothing, and 1 swells about 1mm for reluctantly as it can be seen that 2 be cutaneous protuberance, profile understands, 3 for oedema, and 4 are Oedema is swelled more than 1mm.
It can be seen from the data in table 3 compared with the wet tissue in comparative example 4-19, wet tissue product of the invention has more Small irritation.
4. comfort level
Wet tissue in above-described embodiment and comparative example is used 10 days to red hip baby, the effect such as institute of table 4 after use Show:
The red hip baby of table 4 uses wet tissue effect
It can be seen from the data in table 4 compared with the wet tissue in comparative example, the thing to red hip baby using the present invention After managing antibiotic and sterilizing wet tissue, sufferer improves significantly, suitable for promoting and applying.

Claims (10)

1. a kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue, it is made of wet tissue body and wet tissue liquid, institute It is the non-woven fabrics for being bonded high molecular quaternary to state wet tissue body;The wet tissue liquid is by following each groups with percentage by weight Part composition:
RO purified waters 65-70%
12-18 alkyl glucosides 0.1-0.6%
Lecithin or hydrolecithin 0.2-0.5%
1,2- pentanediol 25-30%
Skin conditioning agent 0.2-2%
Other additives 1-6%,
The sum of each component content is 100%;
Wherein, the preparation method of wet tissue body is:
(1) length is used as 40-50mm, and the bamboo pulp fiber of a diameter of 0.04-0.1mm is as raw material, through cross lapping spun lacing work Bamboo pulp non-woven fabrics is made after skill, the nonwoven carrier that thickness is 3-5mm is obtained after clipped, high-temperature sterilization;
(2) nonwoven carrier made from step (1) is placed in the monomer solution of isopropanol/water mixed solvent preparation, at room temperature When lucifuge immersion 12-24 is small;
(3) under nitrogen protection, CeCl is added in monomer solution3/ HCl/water solution, with warp in x ray irradiation x above-mentioned steps (2) The non-woven fabrics obtained after immersion, irradiation intensity 80-200KGy;
(4) after irradiating, unreacted monomer and homopolymer are fallen in extracting, and wet tissue body is obtained after dry;
Wherein, monomer is organosilicon bi-quaternary ammonium salt and acrylamide, and the mass fraction of organosilicon bi-quaternary ammonium salt is in monomer solution 0.2-0.3%, and the molar ratio of organosilicon bi-quaternary ammonium salt and acrylamide is (10-20): 1;CeCl3At the beginning of in the reaction system Beginning concentration is (1-2) × 10-4The initial concentration of mol/L, HCl in the reaction system is (1-2) × 10-3mol/L;
The organosilicon bi-quaternary ammonium salt is the compound shown in formula 1 or formula 2:
2. acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue as claimed in claim 1, wherein, the ray is selected from Ultraviolet, electron beam, X-ray, alpha ray, β rays or gamma-rays.
3. acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue as claimed in claim 1, wherein, the skin condition Agent is ceramide, the one or more in Co-Q10, tocopherol acetate, resveratrol, astaxanthin.
4. acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue as claimed in claim 1, wherein, other described add Add agent for one or more kinds of mixtures in antioxidant, chelating agent, pH adjusting agent.
5. the acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue as described in claim 1 or 4, wherein, it is described other One or more of the additive in Butylated Hydroxytoluene, EDTA-2Na, EDTA-4Na, arginine, citric acid, sodium citrate Mixture.
6. acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue as claimed in claim 1, wherein, the 12-18 alkane Base glucoside is lauryl glucoside.
7. acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue as claimed in claim 1, wherein, the 12-18 alkane Base glucoside is octadecyl glucoside.
8. the preparation side of the acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue as described in claim 1-7 any one Method, it is characterised in that:
The preparation method of wet tissue body is:
(1) length is used as 40-50mm, and the bamboo pulp fiber of a diameter of 0.04-0.1mm is as raw material, through cross lapping spun lacing work Bamboo pulp non-woven fabrics is made after skill, the nonwoven carrier that thickness is 3-5mm is obtained after clipped, high-temperature sterilization;
(2) nonwoven carrier made from step (1) is placed in the monomer solution of isopropanol/water mixed solvent preparation, at room temperature When lucifuge immersion 12-24 is small;
(3) under nitrogen protection, CeCl is added in monomer solution3/ HCl/water solution, with warp in x ray irradiation x above-mentioned steps (2) The non-woven fabrics obtained after immersion, irradiation intensity 80-200KGy;
(4) after irradiating, unreacted monomer and homopolymer are fallen in extracting, and wet tissue body is obtained after dry;
Wherein, monomer is organosilicon bi-quaternary ammonium salt and acrylamide, and the mass fraction of organosilicon bi-quaternary ammonium salt is in monomer solution 0.2-0.3%, and the molar ratio of organosilicon bi-quaternary ammonium salt and acrylamide is (10-20): 1;CeCl3At the beginning of in the reaction system Beginning concentration is (1-2) × 10-4The initial concentration of mol/L, HCl in the reaction system is (1-2) × 10-3mol/L;
The organosilicon bi-quaternary ammonium salt is the compound shown in formula 1 or formula 2:
Wet tissue liquid is the facial treatment milk of transparent and stable, and its preparation method is:
(1) 12-18 alkyl glucosides 0.1-0.6%, lecithin or hydrolecithin 0.2-0.5% are mixed and heated to 50- 80 DEG C, at this temperature, 5-20min is quickly stirred, to obtaining clear solution A;
(2) RO purified waters 65-70%, 1,2- pentanediols 25-30%, other additives 1-6% are mixed and heated to 60-90 DEG C, it is evenly stirred until clear solution B;
(3) under high-speed stirred, B solution is slowly added in solution A, until obtaining clear solution C;
(4) C solution that cools down adds skin conditioning agent 0.2-2%, stirs evenly and clear solution D is made to less than 45 DEG C;
(5) ozone is passed through in solution D, ozone concentration is maintained in the range of 0.1-1.0mg/L, up to wet tissue liquid E;
Finally, the ratio of wet tissue liquid E and the wet tissue body by weight 1.5: 1-4: 1 for being cut into suitable dimension is added, then Pack, up to acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue.
9. preparation method as claimed in claim 8, wherein ozone concentration are in 0.1-0.5mg/L scopes.
10. preparation method as claimed in claim 8, wherein wet tissue liquid E are with being cut into the wet tissue body of suitable dimension by weight The ratio addition of amount 2: 1-3: 1.
CN201711094247.4A 2017-11-09 2017-11-09 A kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue and preparation method thereof Pending CN107898651A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201711094247.4A CN107898651A (en) 2017-11-09 2017-11-09 A kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201711094247.4A CN107898651A (en) 2017-11-09 2017-11-09 A kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue and preparation method thereof

Publications (1)

Publication Number Publication Date
CN107898651A true CN107898651A (en) 2018-04-13

Family

ID=61843795

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201711094247.4A Pending CN107898651A (en) 2017-11-09 2017-11-09 A kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue and preparation method thereof

Country Status (1)

Country Link
CN (1) CN107898651A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113698444A (en) * 2021-08-25 2021-11-26 太和县芮欣生物科技有限公司 Cationic alkyl glycoside quaternary ammonium salt surfactant and preparation process thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1978501A (en) * 2006-12-08 2007-06-13 北京化工大学 UV-induced polymer surface modifying method
CN101716359A (en) * 2009-12-08 2010-06-02 北京欧凯纳斯科技有限公司 Sterilization and pasteurization material and application thereof
CN103566371A (en) * 2012-08-01 2014-02-12 南京神奇科技开发有限公司 Antimicrobial physical method
CN106038356A (en) * 2016-07-04 2016-10-26 苏州宝丽洁日化有限公司 Physical antibacterial wet wipe and preparation method thereof
CN106726636A (en) * 2017-02-17 2017-05-31 苏州宝丽洁日化有限公司 A kind of physical antibacterial wet tissue
CN106860029A (en) * 2017-02-17 2017-06-20 苏州宝丽洁日化有限公司 A kind of physical antibacterial wet tissue

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1978501A (en) * 2006-12-08 2007-06-13 北京化工大学 UV-induced polymer surface modifying method
CN101716359A (en) * 2009-12-08 2010-06-02 北京欧凯纳斯科技有限公司 Sterilization and pasteurization material and application thereof
CN103566371A (en) * 2012-08-01 2014-02-12 南京神奇科技开发有限公司 Antimicrobial physical method
CN106038356A (en) * 2016-07-04 2016-10-26 苏州宝丽洁日化有限公司 Physical antibacterial wet wipe and preparation method thereof
CN106726636A (en) * 2017-02-17 2017-05-31 苏州宝丽洁日化有限公司 A kind of physical antibacterial wet tissue
CN106860029A (en) * 2017-02-17 2017-06-20 苏州宝丽洁日化有限公司 A kind of physical antibacterial wet tissue

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113698444A (en) * 2021-08-25 2021-11-26 太和县芮欣生物科技有限公司 Cationic alkyl glycoside quaternary ammonium salt surfactant and preparation process thereof

Similar Documents

Publication Publication Date Title
CN106038356B (en) A kind of physical antibacterial wet tissue and preparation method thereof
CN109381480B (en) Compound polyhexamethylene biguanide disinfectant and preparation method thereof
CN106726636A (en) A kind of physical antibacterial wet tissue
CN109381363A (en) A kind of amino acid shampoo and preparation method thereof
CN105209049B (en) Antimicrobial compositions and its manufacturing method
CN106860029B (en) Physical antibacterial wet tissue
CN110327282A (en) A kind of dandruff control shampoo containing and preparation process improving scalp epidermis microbial flora
CN113117137A (en) Medical dressing containing recombinant human collagen and preparation method thereof
US20200297605A1 (en) Biome-friendly consumer products
JPWO2009069619A1 (en) Novel composition containing ozonized surfactant
CN104887578A (en) Silicon-oil-free composition with scalp care function and hair conditioner
CN107929104A (en) A kind of three-in-one wash and maintenance liquid of biology enzyme and preparation method thereof
CN115317392B (en) Oil-control anti-dandruff amino acid shampoo and preparation method thereof
CN107320362A (en) All Pure Nature, support, protect, washing comprehensive, noresidue goes to remain shampoo
CN110974717B (en) Moisturizing baby wet tissue capable of removing dirt and preparation method thereof
KR102272901B1 (en) Composition for external application to the skin containing meso-2,3-butanediol as a preservative
JP2020164548A (en) Composition containing meso-2,3-butanediol
US20200297619A1 (en) Biome-friendly consumer products
TWI329640B (en) Use of substituted 2,4-bis(alkylamino)pyrimidines
CN107898651A (en) A kind of acrylamide organosilicon bi-quaternary ammonium salt grafted nonwoven fabric wet tissue and preparation method thereof
CN109512741A (en) A kind of essential oil is washed one's hands condensation and preparation method thereof
CN109528526A (en) Plant essence skin conditioning agent and preparation method thereof and oil control and acne removal application
CN107440925A (en) A kind of compound method of disposable hand sanitizing fluid
CN107789214A (en) A kind of acrylic acid bi-quaternary ammonium salt grafted nonwoven fabric wet tissue and preparation method thereof
CN104207970A (en) Medical skin-care disinfection hand-cleaning liquid and preparation method 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
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20180413