CN113693954B - Antibacterial hand sanitizer - Google Patents

Antibacterial hand sanitizer Download PDF

Info

Publication number
CN113693954B
CN113693954B CN202111035200.7A CN202111035200A CN113693954B CN 113693954 B CN113693954 B CN 113693954B CN 202111035200 A CN202111035200 A CN 202111035200A CN 113693954 B CN113693954 B CN 113693954B
Authority
CN
China
Prior art keywords
acid
hand sanitizer
sodium
deionized water
anode
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.)
Active
Application number
CN202111035200.7A
Other languages
Chinese (zh)
Other versions
CN113693954A (en
Inventor
梁莲芝
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.)
Swashes Products Co ltd
Original Assignee
Swashes Products 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 Swashes Products Co ltd filed Critical Swashes Products Co ltd
Priority to CN202111035200.7A priority Critical patent/CN113693954B/en
Publication of CN113693954A publication Critical patent/CN113693954A/en
Application granted granted Critical
Publication of CN113693954B publication Critical patent/CN113693954B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/20Halogens; Compounds thereof
    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/26Aluminium; Compounds thereof
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42Amides
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • A61K8/442Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
    • 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
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/466Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • 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
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9789Magnoliopsida [dicotyledons]
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00Electrolytic production of inorganic compounds or non-metals
    • C25B1/01Products
    • C25B1/22Inorganic acids
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00Electrolytic production of inorganic compounds or non-metals
    • C25B1/01Products
    • C25B1/24Halogens or compounds thereof
    • C25B1/26Chlorine; Compounds 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
    • A61K2800/48Thickener, Thickening system
    • 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
    • A61K2800/59Mixtures
    • A61K2800/592Mixtures of compounds complementing their respective functions
    • A61K2800/5922At least two compounds being classified in the same subclass of A61K8/18
    • 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
    • A61K2800/59Mixtures
    • A61K2800/596Mixtures of surface active compounds
    • 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
    • A61K2800/80Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/805Corresponding aspects not provided for by any of codes A61K2800/81 - A61K2800/95

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Dermatology (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Emergency Medicine (AREA)
  • Biotechnology (AREA)
  • Botany (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Apparatus For Disinfection Or Sterilisation (AREA)

Abstract

The invention provides an antibacterial hand sanitizer, which is characterized in that the hand sanitizer is compounded with anionic surfactant, amphoteric surfactant and nonionic surfactant to obtain efficient foaming and decontamination performance, hypochlorous acid is used as a sterilization raw material, the sterilization and decontamination capability is strong, the sterilization pair number of the hand sanitizer in 2 minutes is about 4.48, and the hand sanitizer has the performances of skin care, skin moisturizing, antibacterial, anti-allergy, relieving and strong sterilization and decontamination capability.

Description

Antibacterial hand sanitizer
Technical Field
The invention belongs to the field of detergents, and particularly relates to an antibacterial hand sanitizer.
Background
As a novel hand cleaning product, the hand sanitizer replaces the soap commonly used in the past in public places such as hotels, catering departments, airports and the like. Compared with soap, the hand sanitizer has the unique advantage that the hand sanitizer can avoid contacting hands, prevents dirt, bacteria, viruses and the like from being polluted after use or in the environment to become a secondary pollution source, is easy to store and has less natural consumption. The soap has strong dependence on mechanical rubbing in the process of smearing and using, is in a wet state for a long time when being used in public places, and is beneficial to bacterial and virus breeding.
The hand sanitizer has the characteristics of flexible and changeable formula, strong plasticity, easy improvement, mild performance, no skin irritation, hard water resistance, abundant foam, diversified components and easy processing, and various hand sanitizer products on the market can be roughly divided into: (1) common hand cleanser: no special component is added, and the effect of removing dirt and grease on hands is generally achieved; (2) skin care type hand sanitizer: pure glycerin, aloe and other skin care components are added into the hand sanitizer, so that the hand sanitizer has the function of moistening skin while cleaning hands; (3) heavy oil dirt type hand sanitizer: the soap is mainly suitable for workers in the industries of machine repair, oil refining, automobile repair and the like, the hands of the workers are often stained with heavy oil stains, and common soaps and hand sanitizers are difficult to clean; (4) disinfectant and sterilization type hand sanitizer: the effective bactericidal component is added into the hand sanitizer to solve the existing public health problems, so that the spread of diseases can be blocked; (5) Water-free type
Hand sanitizer: alcohol is generally used as a main component, water is not needed for washing, the use is simple and convenient, and the hand cleaner is generally used for cleaning and disinfecting hands under the condition of water deficiency; (6) other functional hand sanitizers: aiming at different consumer groups, special-function hand sanitizers, such as lead-removing hand sanitizer, composite-function hand sanitizer and the like are developed. The hand sanitizer has rich variety and function, also proves that the hand sanitizer is easy to process, has strong product plasticity and wide market prospect, and can play a more important role in preventing diseases.
Hypochlorous acid is the most effective disinfectant in chlorine-containing dilute solution, is usually prepared by an electrochemical method, is acidic electrolyzed water, is water with pH of 5.0-6.5 and effective chlorine concentration of 10-30mg/L, has strong oxidizing ability and rapid microorganism killing effect, and is widely used in hand sanitizers.
For example, CN 111481452A of Shandong Shuda biotechnology limited discloses a seed safety protection hand sanitizer and a preparation method thereof, wherein the seed safety protection hand sanitizer comprises the following components: the environment-friendly water-based paint comprises weak acid sodium hypochlorite solution, 0-phenylphenol, polyhexamethylene guanidine hydrochloride, chloroxylenol, quaternary ammonium salt, chlorhexidine acetate, glycerin and surfactant, wherein the weak acid sodium hypochlorite solution contains 50-100 mg/L of available chlorine, and the pH value range is 5-7. . The preparation method comprises the following specific steps: step one: respectively diluting hydrochloric acid and sodium hypochlorite solution with water, and fully mixing; step two: fully reacting the solution in the first step in a reactor; step three: adding the rest components into the weak acid sodium hypochlorite solution prepared in the second step, stirring and uniformly mixing by a stirring device, and bottling and packaging. Compared with the prior art, the invention has the advantages that: the sterilizing agent does not contain alcohol components, is colorless and odorless, is safe and convenient to use, does not generate secondary pollution after sterilization, and has good sterilizing and bacteriostasis effects.
Furthermore, as in CN201110066196a similar to the present invention, a natural disinfecting and washing composition without preservatives is disclosed, which has both disinfecting and washing functions, said composition containing electrolytic chlorine oxidizing agent, APG, for washing the off-flavors of tableware, cookware, vegetables, melons, fabrics, or sweaty feet, sweat socks, the electrolytic chlorine oxidizing agent containing hypochlorite ions and hypochlorous acid, obtained by electrolyzing a dilute solution of sodium chloride in a diaphragm-free electrolytic cell.
Disclosure of Invention
Based on the above, the invention provides the antibacterial hand sanitizer, which takes hypochlorous acid as a sterilizing substance, has extremely strong sterilizing effect on escherichia coli, staphylococcus aureus and candida albicans, is clean, environment-friendly, safe and good in decontamination effect, and is a safe and effective daily article.
The invention also adopts special anodic electrolytic sodium chloride to prepare high-efficiency hypochlorous acid solution, the binding force between the substrate and the active layer is obviously improved by designing a micro-arc oxidation intermediate layer, the metal oxide has long service life of strengthening electrolysis, and the (Ir-Nb-Rh) Ox active layer is prepared to realize Ti-W-Ir-Nb-Rh compounding, so that the electrode with high catalytic activity, high corrosion resistance and high conductivity is obtained, the oxygen and chlorine evolution potential is reduced, the electrochemical conversion efficiency is improved, and the anode current efficiency is 85.3-94.2%.
The antibacterial hand sanitizer comprises an alpha-olefin sodium sulfonate AOS anionic surfactant, a cocamide propyl betaine CAB-35 amphoteric surfactant, a coco fatty acid monoethanolamide CMEA nonionic surfactant, a glycerin humectant, sodium chloride inorganic salt, a polyacrylic acid PPA thickener, disodium ethylenediamine tetraacetate EDTA-2Na, a mica powder pearlescent additive, lemon essence and hypochlorous acid deionized water solution, wherein the pH of the hand sanitizer is 5.75-6.75, and the viscosity is 2000-4000 mPa.S.
Further, the hand sanitizer comprises the following components:
alpha-olefine sodium sulfonate AOS anionic surfactant: 7-9wt.%;
cocamide propyl betaine CAB-35 amphoteric surfactant: 6-7 wt%;
coconut fatty acid monoethanolamide CMEA nonionic surfactant: 5-6 wt%;
glycerin humectant: 1-3 wt%;
sodium chloride inorganic salt: 0.01-0.12 wt%;
polyacrylic acid PPA thickener: 1-4 wt%;
disodium edetate EDTA-2Na:0.05-0.12 wt%;
mica powder pearlescent additive 0.5-1 wt%;
lemon essence: 0.1-1.0%;
hypochlorous acid deionized water solution: the balance.
Further, the effective chlorine component in the hand sanitizer is 50-70ppm.
Further, the aqueous sodium hypochlorite solution is prepared by the following method:
(1) And (3) setting a reaction tank: the reaction tank at least comprises a Ti/TiO2-WO 3/(Ir-Nb-Rh) Ox anode, and a titanium alloy or stainless steel is used as a cathode:
(2) Electrolytic sodium chloride: introducing a mixed solution of saturated saline and hydrochloric acid into the bottom of the reaction tank;
(3) Dilution and collection of hypochlorous acid disinfectant: the effluent was collected from the top of the electrolyzer and then diluted with deionized water to obtain hypochlorous acid sterilizing water.
The preparation method of the Ti/TiO2-WO 3/(Ir-Nb-Rh) Ox anode comprises the following steps:
(a) Pretreating a titanium plate or a titanium mesh substrate;
(b) Preparing a TiO2-WO3 composite intermediate layer on the surface of a substrate: taking the pretreated substrate as an anode, and placing the anode in electrolyte for micro-arc oxidation treatment, wherein the electrolyte consists of sodium tungstate trihydrate, sodium hydroxide, sodium fluoride, sodium hexametaphosphate and deionized water;
electrolytic parameters: the bidirectional pulse voltage is 350-400V positive pressure, 30-50V negative pressure, duty ratio is 30-40%, frequency is 700-800Hz, positive and negative pulse ratio is 1:1, time is 4-8min, and thickness of the middle layer is 5-10 mu m;
(c) Preparation of (Ir-Nb-Rh) Ox active layer: to a certain amount of NbCl 4 Dissolving in isopropanol, dissolving a certain amount of ammonium chlororhodium and iridium in a mixed solution of isopropanol and hydrochloric acid in a ratio of 1:1, mixing the ammonium chloroiridium, the ammonium chlororhodium and niobium tetrachloride according to a molar ratio of (10-25) to (15-20) to (5-10) to obtain a precursor solution, brushing the precursor solution on the surface of the TiO2-WO3 composite intermediate layer, drying at 60-70 ℃ for 3-5min, converting a muffle furnace, heating the muffle furnace to a temperature of 5 ℃/min to 450-500 ℃, maintaining for 20-30min, naturally cooling, repeating the brushing process until the required load is reached, and annealing at 450-500 ℃ for 1-1.5h to obtain the Ti/TiO2-WO 3/(Ir-Nb-Rh) Ox anode.
Further, the pretreatment comprises degreasing, sand blasting and flushing, wherein the degreasing comprises the steps of: placing the substrate in 3-5wt.% Na 2 CO 3 Maintaining the solution for 5-10min, and then 60-80 o C, ultrasonic treatment for 1-3min; sand blasting and coarsening: quartz sand with 0.1-0.5mm, the hardness is approximately equal to 400HV, and the air pressure is 0.1-0.15MPa; the flushing is deionized water flushing.
Further, the sodium tungstate trihydrate is 13-17g/L, the sodium hydroxide is 1.5-2.5g/L, the sodium fluoride is 2-3g/L, the sodium hexametaphosphate is 4-5g/L, and the balance is deionized water.
Further, the thickness of the TiO2-WO3 composite intermediate layer is 5-10 mu m, and the thickness of the (Ir-Nb-Rh) Ox active layer is 12-15 mu m.
Further, the loading in the step (c) is 2.2-2.5mg/cm 2
The hand sanitizer is a cleaning product designed for removing stains and bacteria on hands, and consists of necessary active ingredients, sterilization ingredients and auxiliary ingredients.
And (2) a surfactant: the basic function is cleaning function, the hand cleaner mainly cleans greasy dirt on hands, the surfactant can generate abundant foam, the surfactant is dissolved in water at a lower concentration, the surface tension of a solution system can be greatly reduced, a large number of micelles can be formed in the solution along with the fact that the surfactant reaches the critical micelle concentration, and the micelles can play roles in wetting, solubilizing, emulsifying and dispersing to clean the greasy dirt.
Humectant: for market demands, not only simple cleaning and decontamination, but also human body feeling after cleaning is very important, and dryness and roughness of hands are avoided, so that a humectant is required to improve body feeling, and the humectant is defined as a substance capable of keeping moisture in the stratum corneum of skin or delaying and preventing volatilization of moisture in the stratum corneum, and particularly can show the characteristic under low humidity.
And (3) a thickening agent: when the hand sanitizer is used, if the viscosity is too small, the hand sanitizer is very easy to slide away from hands, waste is caused, the detergency is also affected, and the viscosity is adjusted to be too large, so that the hand sanitizer is not easy to squeeze and rinse. The hand sanitizer has proper viscosity, can enhance the sensory effect of consumers, and adopts sodium chloride and polyacrylic acid PPA as thickening agents.
Complexing agent: the usual water quality contains Ca 2+ 、Mg 2+ Some surfactants are relatively poor in hard water resistance and precipitate with metal ions in such water to affect the performance of the detergent. The complexing agent is added into the detergent, can be complexed with the metal ions to be eliminated in the form of a dissolved complex, so that hard water is softened, EDTA-2Na is adopted as the complexing agent, the complexing agent can form a soluble annular structure in water, and the metal ions are bound in the annular structure, so that the metal ions are prevented from forming precipitates, and the solution has a good appearance.
Essence and pearl powder are used for improving the touch effect of the hand washing liquid, and the taste and the appearance required by customers can be selected according to the needs.
A bactericide: because hypochlorous acid is uncharged and has relatively low molecular weight, the hypochlorous acid can penetrate cell walls more than other bactericides or bacteriostats, and has higher oxidation reaction speed with organic matters (namely key components of microbial cells), so that the sterilizing effect is more efficient, and the aim of killing bacterial propagules, viruses, fungi, tubercle bacillus and bacterial spores can be fulfilled by penetrating cell membranes in a mode of attacking physiologically relevant molecules (ammonia, thioether, mercaptan, nucleotide and the like) only under the condition of low concentration so as to oxidize proteins.
Regarding the electrolysis process and anode used in the present invention:
first,: the method comprises the steps of pre-treating the surface of a titanium substrate, wherein the surface treatment comprises degreasing and sand blasting, the degreasing step is an unnecessary treatment process, mainly because micro-arc oxidation is carried out later, the micro-arc oxidation process has larger voltage, and an obvious anodic electrochemical degreasing process can occur, so that degreasing is unnecessary, but the degreasing can influence the bonding force between a micro-arc oxidation layer and the substrate to a certain extent, therefore, the method is used for pre-degreasing the substrate, and the substrate is subjected to sand blasting after degreasing, wherein the main purpose of sand blasting is not to remove oxidation, the main purpose of sand blasting is to improve the surface roughness of the substrate, and the impurity on the surface is removed, so that the bonding area of the substrate and a micro-arc oxidation intermediate layer can be obviously improved by sand blasting, and the bonding force between the substrate and an active layer is further improved.
Secondly, regarding the middle layer, the middle layer has the functions of increasing the binding force between the titanium matrix and the active coating, resisting gas scouring, preventing the coating from peeling off prematurely, simultaneously, the existence of the middle layer also blocks the diffusion and permeation of oxygen to the matrix, slows down the formation speed of the non-conductive titanium oxide film between the matrix and the active layer, delays the passivation and deactivation of the matrix, and improves the service life of the oxide anode
And (5) a life. The intermediate layer in the prior art is mainly an intermediate layer such as SnO2, sn-Sb oxide, ir-Co oxide, sn-Sb-Mn oxide, sn-Ru-Mn oxide, ru-Sn-Sb oxide, ru-Sb-Mn oxide, nb-Sn oxide and the like, and of course, part of the intermediate layer is a titanium-based anode oxide film, the intermediate layer is a titanium-based micro-arc oxide film, the bonding force between a substrate and an intermediate layer can be effectively improved by taking the anode oxide film or the micro-arc oxide film as the intermediate layer, mainly because the oxide film is generated in situ, no obvious interface exists between the intermediate layer on the surface of the titanium substrate and the substrate, the transition is good, and the coating, electroplating or other deposition methods have obvious interfaces, when the interface is used for subsequent heat treatment of an active layer, certain heat stripping or heat stress accumulation can be necessarily generated, in addition, compared with an anodic oxide film, the micro-arc oxide film is far higher than the micro-arc oxide film in corrosion resistance (salt spray resistance), hardness and service life, but the micro-arc oxide film has lower porosity in morphology, so that the binding force between an active coating and a substrate is reduced, the surface of the pure titanium oxide micro-arc oxide film is rough, discharge residual holes with different sizes exist, the range of the holes is large, the porosity is about 2-8wt.%, the main contribution of the porosity is a surface porous layer, the physical and chemical contribution is a transition layer, the binding force is a dense layer at the bottom, the pore absorption rate of the dense layer is lower than 1%, and the specific surface area of the micro-arc oxide sliding film is 10.32m 2 And/g. In contrast, the W element is added in the micro-arc oxidation film, so that the micro-arc oxidation film has higher porosity and the specific surface area is increased to 13.9 m 2 The improvement of the porosity and the surface area obviously improves the contact area of the intermediate layer and the active layer, improves the binding force of the intermediate layer and the active layer, and also provides the active layer in the composite synergistic activation processMore active sites, tiO in the intermediate layer obtained 2 About 50-55wt.%, and about 25-30wt.% W, the Ti component being more due to Ti 4+ Takes part in at least two main reactions, and W takes part in at least one main reaction, the reaction formula is as follows:
Ti 4+ +2OH - +2H 2 O→TiO 2 +2H2O +
Ti 4+ +2WO 4 2- +TiO 2 +2WO 3
namely, the TiO2-WO3 has the beneficial effects of corrosion resistance, good conductivity and tight combination with the titanium matrix.
Active layer: the two or more components mixed in the electrode seek a synergistic effect to achieve a close electronic relationship between the components
The invention adopts Ir, nb and Rh as main active elements, namely Ir, nb and Rh as main elements of the coating, wherein Ir and Rh are main oxides, high catalytic activity and corrosion resistance are provided, nb is used for improving the form of oxide particles on the surface of the coating, refining the coating grains, increasing the microscopic area of the electrode, having larger roughness and improving the specific surface area of the surface activity, and further improving the catalytic activity of the coating.
The (Ir-Nb-Rh) Ox solid solution of the invention can not be completely dissolved, and part of the solution can be separated out by IrOX and RuO2, so that the microcosmic specific surface area and active site of the anode can be increased, the chlorine separation efficiency is improved, a large number of micropores and gaps are formed on the surface of the electrode, obvious crystal clusters are separated out from the gaps, the microcosmic specific surface area is increased, the current density is small, the service life of the electrode is prolonged, and the coating has flat surface, compact crystallization, shallow crack depth, narrow width and fine crack.
The invention relates to a process for electrolyzing hypochlorous acid, which adopts a diaphragm-free electrolytic tank, wherein the reaction tank at least comprises a Ti/TiO2-WO 3/(Ir-Nb-Rh) Ox anode, a titanium alloy or stainless steel is used as a cathode, the anode is used for chlorine separation reaction, namely chlorine ions lose electrons to form chlorine molecules, and meanwhile, the chlorine reacts with water to generate hypochlorous acid and chlorine ions, and a small part of the chlorine molecules are generatedAnd chlorate ions. Meanwhile, oxygen is separated out after water molecules of the anode are electrolyzed, the oxygen separation reaction is a side reaction, the oxygen separation reaction is avoided as much as possible, in the competition of the chlorine separation reaction and the oxygen separation reaction, the chlorine separation reaction is used for dominating, but when the concentration of the sodium chloride electrolyte is too low, ionized chloride ions cannot meet the electrolysis speed of an electrolytic tank, so that water electrolysis is started, oxygen is separated out, the oxygen defect of anode active oxides is obviously reduced due to the separation of the oxygen, the catalytic layer is deactivated, and the current density is as follows: the current density of the invention is 100-150 mA/cm 2 The available chlorine increased with increasing current density, the pH was slowly shifted to neutral, the chlorine evolution potential was significantly decreased, as in example 3, after increasing current density, the chlorine evolution potential was 0.98V, lower than that of example 2, and the current efficiency was decreased with increasing current density, mainly due to oxygen evolution competition reaction.
The effluent of the present invention had a pH of 2.5 to 4, in which the hypochlorous acid was hardly preserved, approximately within 20 to 30 days, and the available chlorine of the obtained effluent was almost zero, so that the newly obtained effluent had to be diluted to a pH of 6.5 to 7, the effluent obtained as in example 2 was diluted to a ph=6.75 using deionized water, the content of available chlorine was tested under a sealed condition for various times in a dark place, the initial available chlorine content was 62mg/L, the preservation rate of available chlorine was 97% after 120 days, the preservation effect was excellent, the sterilizing effect on escherichia coli and staphylococcus aureus was tested on available chlorine preserved under a sealed dark place, the ORP value was 1040mV, the available chlorine was about 60 mg/L, and the sterilizing effect was almost 100% within 3 minutes.
The beneficial technical effects are as follows:
(1) The efficient foaming and decontamination performance is obtained by compounding the anionic surfactant, the amphoteric surfactant and the nonionic surfactant into the surfactant.
(2) The hand sanitizer has the advantages of skin care, skin moisturizing, antibiosis, bacteriostasis, allergy relief, strong sterilization and decontamination capability, the sterilization efficiency of escherichia coli and staphylococcus aureus in 1min is 99.99%, and the sterilization logarithmic value in 2min is 4.48 (99.99668%).
(3) The TiO2-WO3 intermediate layer is prepared on the surface of the titanium substrate by in-situ oxidation, so that the binding force of the substrate titanium and the active layer is effectively improved, the specific surface area of the intermediate layer is relatively high, the microcosmic contact specific surface area is provided for coating the active layer, and the stability between the intermediate layer and the active layer is further improved.
(4) The solid solution active components mainly containing Ir, nb and Rh are coated on the surface of the intermediate layer, so that the catalytic activity of electrolysis is obviously improved, the coating grains are thinned, the obtained coating has flat surface, compact crystallization, shallow crack depth and narrow width, and has fine cracks, and the catalytic activity, stability and service life of the coating are improved.
(5) The chlorine evolution potential of hypochlorous acid prepared by electrolyzing sodium chloride is low, the current efficiency is high, the effective chlorine concentration is high, and the sterilization effect is excellent.
The specific embodiment is as follows:
all hypochlorous acid preparation processes of examples 1-3 of the present invention were as follows:
a method for preparing a disinfectant, wherein the disinfectant is hypochlorous acid, and the method comprises the following steps:
(1) And (3) setting a reaction tank: the reaction tank at least comprises a Ti/TiO2-WO 3/(Ir-Nb-Rh) Ox anode, a titanium alloy or stainless steel is used as a cathode, and the pole distance between the cathode and the anode is 3.5mm.
(2) Electrolytic sodium chloride: introducing a mixed solution of saturated saline and hydrochloric acid into the bottom of the reaction tank, wherein the pH value of the mixed solution is 0.9, the mixing liquid inlet speed is 1.5L/h, and the current density is 125mA/cm 2
(3) Dilution and collection of hypochlorous acid disinfectant: the effluent was collected from the top of the electrolyzer and then used and diluted with deionized water.
The preparation method of the Ti/TiO2-WO 3/(Ir-Nb-Rh) Ox anode is as follows.
(a) Pretreatment of titanium plates or titanium mesh substrates: the pretreatment comprises degreasing, sand blasting and flushing, wherein the degreasing comprises the following steps: placing the substrate in 4wt.% Na 2 CO 3 The solution was kept for 7.5min, then 70 o C, ultrasonic treatment for 2min; sand blasting and coarsening: quartz sand with 0.1-0.5mm, hardnessAbout 400HV, air pressure 0.125MPa; the flushing is deionized water flushing.
(b) Preparing a TiO2-WO3 composite intermediate layer on the surface of a substrate: the pretreated substrate is taken as an anode and placed in electrolyte for micro-arc oxidation treatment, wherein the electrolyte consists of sodium tungstate trihydrate, sodium hydroxide, sodium fluoride, sodium hexametaphosphate and deionized water, the sodium tungstate trihydrate is 15g/L, the sodium hydroxide is 2g/L, the sodium fluoride is 2.5g/L, the sodium hexametaphosphate is 4.5g/L, and the balance is deionized water.
Electrolytic parameters: bidirectional pulse voltage, positive pressure 375V, negative pressure 40V, duty ratio 35%, frequency 750Hz, positive and negative pulse ratio 1:1, time 6min.
(c) Preparation of (Ir-Nb-Rh) Ox active layer: to a certain amount of NbCl 4 Dissolving ammonium chlororhodium and chloroiridium in isopropanol, dissolving a certain amount of ammonium chlororhodium and chloroiridium in a mixed solution of isopropanol and hydrochloric acid in a ratio of 1:1, mixing chloroiridium, ammonium chlororhodium and niobium tetrachloride according to a molar ratio of (17.5) to (7.5) to obtain a precursor solution, coating the precursor solution on the surface of a TiO2-WO3 composite intermediate layer by using a brush, drying at 70 ℃ for 5min, converting a muffle furnace, heating the muffle furnace to a temperature of 5 ℃/min to 475 ℃, maintaining for 25min, naturally cooling, and repeating the brushing process until the required concentration is 2.35mg/cm 2 The supported amount was then annealed at 475℃for 1.25h to obtain a Ti/TiO2-WO 3/(Ir-Nb-Rh) Ox anode.
Example 1
Alpha-olefine sodium sulfonate AOS anionic surfactant: 7wt.%;
cocamide propyl betaine CAB-35 amphoteric surfactant: 6 wt%;
coconut fatty acid monoethanolamide CMEA nonionic surfactant: 5 wt%;
glycerin humectant: 1wt.%;
sodium chloride inorganic salt: 0.01-0.12 wt%;
polyacrylic acid PPA thickener: 1-4 wt%;
disodium edetate EDTA-2Na complexing agent: 0.05-0.12 wt%;
mica powder pearlescent additive 0.5-1 wt%;
lemon essence: 0.1-1.0%;
hypochlorous acid deionized water solution with available chlorine of 60 ppm: the balance.
The pH was 5.75.
Example 2
Alpha-olefine sodium sulfonate AOS anionic surfactant: 7-9wt.%;
cocamide propyl betaine CAB-35 amphoteric surfactant: 6-7 wt%;
coconut fatty acid monoethanolamide CMEA nonionic surfactant: 5-6 wt%;
glycerin humectant: 1-3 wt%;
sodium chloride inorganic salt: 0.01-0.12 wt%;
polyacrylic acid PPA thickener: 1-4 wt%;
disodium edetate EDTA-2Na complexing agent: 0.05-0.12 wt%;
mica powder pearlescent additive 0.5-1 wt%;
lemon essence: 0.1-1.0%;
hypochlorous acid deionized water solution with available chlorine of 60 ppm: the balance.
The pH was 6.2.
Example 3
Alpha-olefine sodium sulfonate AOS anionic surfactant: 7-9wt.%;
cocamide propyl betaine CAB-35 amphoteric surfactant: 6-7 wt%;
coconut fatty acid monoethanolamide CMEA nonionic surfactant: 5-6 wt%;
glycerin humectant: 1-3 wt%;
sodium chloride inorganic salt: 0.01-0.12 wt%;
polyacrylic acid PPA thickener: 1-4 wt%;
disodium edetate EDTA-2Na complexing agent: 0.05-0.12 wt%;
mica powder pearlescent additive 0.5-1 wt%;
lemon essence: 0.1-1.0%;
hypochlorous acid deionized water solution with available chlorine of 60 ppm: the balance.
The pH was 6.75.
The hand sanitizer obtained in example 2 was subjected to foaming test, and the foam stability was reduced by 43% after 5 to 7% after the foam was reduced by 0 to 3 minutes and after 1 hour, the viscosity was measured as 3752 mPa.S according to GB/T13173.6 test for foaming force of detergent, bubble ratio was 372%. The sterilization efficiency of the escherichia coli and staphylococcus aureus in 1min is 99.8%, and the sterilization logarithmic value in 5min is 4.48 (99.99668%).
While the invention has been described in conjunction with specific embodiments, those skilled in the art will appreciate numerous modifications and variations therefrom. It is, therefore, to be understood that the appended claims are intended to cover all such modifications and changes as fall within the true spirit and scope of the invention.

Claims (3)

1. A preparation method of an antibacterial hand sanitizer is characterized by comprising the following components of alpha-olefine sodium sulfonate AOS anionic surfactant, cocamide propyl betaine CAB-35 amphoteric surfactant, cocoanut fatty acid monoethanolamide CMEA nonionic surfactant, glycerol humectant, sodium chloride inorganic salt, polyacrylic acid PPA thickener, ethylene diamine tetraacetic acid EDTA-2Na complexing agent, mica powder pearlescent additive, lemon essence and hypochlorous acid deionized water solution;
wherein the hypochlorous acid deionized water solution is prepared by the following method:
(1) And (3) setting a reaction tank: the reaction tank at least comprises one Ti/TiO 2 -WO 3 /(Ir-Nb-Rh)O x Anode, a titanium alloy or stainless steel is used as cathode:
(2) Electrolytic sodium chloride: introducing a mixed solution of saturated saline and hydrochloric acid into the bottom of the reaction tank;
(3) Dilution and collection of hypochlorous acid disinfectant: collecting effluent liquid from the top of the electrolytic tank, and then diluting with deionized water to obtain hypochlorous acid deionized water solution;
the Ti/TiO 2 -WO 3 /(Ir-Nb-Rh)O x The preparation method of the anode comprises the following steps:
(a) Pretreating a titanium plate or a titanium mesh substrate;
(b) Preparation of TiO on the surface of a substrate 2 -WO 3 A composite intermediate layer: taking the pretreated substrate as an anode, and placing the anode in electrolyte for micro-arc oxidation treatment, wherein the electrolyte consists of sodium tungstate trihydrate, sodium hydroxide, sodium fluoride, sodium hexametaphosphate and deionized water;
electrolytic parameters: the bidirectional pulse voltage is 350-400V positive pressure, 30-50V negative pressure, duty ratio is 30-40%, frequency is 700-800Hz, positive and negative pulse ratio is 1:1, time is 4-8min, and thickness of the middle layer is 5-10 mu m;
(c) Preparation of (Ir-Nb-Rh) O x Active layer: to a certain amount of NbCl 4 Dissolving ammonium chlororhodium and chloroiridium acid in isopropanol, dissolving a certain amount of ammonium chlororhodium and chloroiridium acid in a mixed solution of isopropanol and hydrochloric acid in a ratio of 1:1, mixing ammonium chlororhodium, chlororhodium acid and niobium tetrachloride according to a molar ratio of (10-25) to (15-20) to (5-10) to obtain a precursor solution, and brushing and coating the precursor solution on TiO 2 -WO 3 Drying the surface of the composite intermediate layer at 60-70 ℃ for 3-5min, converting a muffle furnace, heating the muffle furnace to 450-500 ℃ at a temperature of 5 ℃/min, maintaining for 20-30min, naturally cooling, repeating the brushing process until the required load is reached, and then annealing at 450-500 ℃ for 1-1.5h to obtain Ti/TiO 2 -WO 3 /(Ir-Nb-Rh)O x And an anode.
2. The method for preparing the antibacterial hand sanitizer according to claim 1, which is characterized by comprising the following components:
alpha-olefine sodium sulfonate AOS anionic surfactant: 7-9wt.%;
cocamidopropyl betaine CAB-35 amphoteric surfactant: 6-7 wt%;
coconut fatty acid monoethanolamide CMEA nonionic surfactant: 5-6 wt%;
glycerin humectant: 1-3 wt%;
sodium chloride inorganic salt: 0.01-0.12 wt%;
polyacrylic acid PPA thickener: 1-4 wt%;
disodium edetate EDTA-2Na complexing agent: 0.05-0.12 wt%;
0.5-1wt.% of mica powder pearlescent additive;
lemon essence: 0.1-1.0wt.%;
hypochlorous acid deionized water solution: the balance;
the pH of the hand sanitizer is 5.75-6.75, and the viscosity is 2000-4000 mPa.S.
3. The method for preparing the antibacterial hand sanitizer according to claim 1, which is characterized by comprising the following components:
alpha-olefine sodium sulfonate AOS anionic surfactant: 7wt.%;
cocamide propyl betaine CAB-35 amphoteric surfactant: 6 wt%;
coconut fatty acid monoethanolamide CMEA nonionic surfactant: 5 wt%;
glycerin humectant: 1wt.%;
sodium chloride inorganic salt: 0.01-0.12 wt%;
polyacrylic acid PPA thickener: 1-4 wt%;
disodium edetate EDTA-2Na complexing agent: 0.05-0.12 wt%;
0.5-1wt.% of mica powder pearlescent additive;
lemon essence: 0.1-1.0wt.%;
hypochlorous acid deionized water solution with available chlorine of 60 ppm: the balance;
the pH was 5.75.
CN202111035200.7A 2021-09-05 2021-09-05 Antibacterial hand sanitizer Active CN113693954B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202111035200.7A CN113693954B (en) 2021-09-05 2021-09-05 Antibacterial hand sanitizer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202111035200.7A CN113693954B (en) 2021-09-05 2021-09-05 Antibacterial hand sanitizer

Publications (2)

Publication Number Publication Date
CN113693954A CN113693954A (en) 2021-11-26
CN113693954B true CN113693954B (en) 2024-02-20

Family

ID=78660065

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202111035200.7A Active CN113693954B (en) 2021-09-05 2021-09-05 Antibacterial hand sanitizer

Country Status (1)

Country Link
CN (1) CN113693954B (en)

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4377454A (en) * 1980-05-09 1983-03-22 Occidental Chemical Corporation Noble metal-coated cathode
US4468416A (en) * 1981-05-19 1984-08-28 Permelec Electrode Ltd. Electrolytic electrodes having high durability and process for the production of same
US5587058A (en) * 1995-09-21 1996-12-24 Karpov Institute Of Physical Chemicstry Electrode and method of preparation thereof
CN1433270A (en) * 1999-12-10 2003-07-30 花王株式会社 Microbicide compositions
EP2055807A1 (en) * 2007-10-31 2009-05-06 Daiki Ataka Engineering Co., Ltd. Oxygen Evolution Electrode
CN102839387A (en) * 2012-09-20 2012-12-26 福州大学 Titanium anode having Ru-Ir-Ti ternary coating with embedded structure and preparation method thereof
CN111188052A (en) * 2020-02-27 2020-05-22 上海广锋生物科技有限公司 Preparation method of high-performance hypochlorous acid
CN111437206A (en) * 2020-05-27 2020-07-24 珠海纳金科技有限公司 Antibacterial and disinfectant hand sanitizer containing nano-silver and preparation method thereof
CN113072138A (en) * 2021-03-22 2021-07-06 浙江大学 Preparation method of long-life DSA electrode capable of being used for frequently reversing cathode and anode

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4377454A (en) * 1980-05-09 1983-03-22 Occidental Chemical Corporation Noble metal-coated cathode
US4468416A (en) * 1981-05-19 1984-08-28 Permelec Electrode Ltd. Electrolytic electrodes having high durability and process for the production of same
US5587058A (en) * 1995-09-21 1996-12-24 Karpov Institute Of Physical Chemicstry Electrode and method of preparation thereof
CN1433270A (en) * 1999-12-10 2003-07-30 花王株式会社 Microbicide compositions
EP2055807A1 (en) * 2007-10-31 2009-05-06 Daiki Ataka Engineering Co., Ltd. Oxygen Evolution Electrode
CN102839387A (en) * 2012-09-20 2012-12-26 福州大学 Titanium anode having Ru-Ir-Ti ternary coating with embedded structure and preparation method thereof
CN111188052A (en) * 2020-02-27 2020-05-22 上海广锋生物科技有限公司 Preparation method of high-performance hypochlorous acid
CN111437206A (en) * 2020-05-27 2020-07-24 珠海纳金科技有限公司 Antibacterial and disinfectant hand sanitizer containing nano-silver and preparation method thereof
CN113072138A (en) * 2021-03-22 2021-07-06 浙江大学 Preparation method of long-life DSA electrode capable of being used for frequently reversing cathode and anode

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Supported IrxRu1-xO2 Anode Catalysts for PEM-Water Electrolysis;Baumanm,N;Cremers,C;FUEL CELLS;第17卷(第2期);259-267 *
纳米TiO2-Ti基IrO2涂层钛阳极的制备及其性能研究;霍淑利;《中国优秀硕士学位论文全文数据库(电子期刊)》;B014-384 *
钛基涂层不溶性阳极的开发与研究进展;胡新发;刘全兵;廖世军;;材料保护(08);41-45 *

Also Published As

Publication number Publication date
CN113693954A (en) 2021-11-26

Similar Documents

Publication Publication Date Title
Malik et al. Anti-corrosion ability of surfactants: a review
EP1899081A1 (en) Method for cleaning, sterilising and disinfecting dishes and other kitchen utensils and cleaning device
US8603392B2 (en) Electrolyzed water system
US20130125316A1 (en) System and a Method for Washing, Cleaning, Disinfecting and Sanitizing Laundry Using Electrolytic Cell Having Boron-Doped Diamond Electrode
WO2001066682A1 (en) Cleaning solution, and method and apparatus for cleaning using the same
WO1999037414A1 (en) Washing process and washing unit
CN101775635A (en) Treatment process of stainless steel cold-rolled sheet
CN102517603A (en) Preparation method for titanium-based low-precious-metal-content oxide coating anode
CN110055548A (en) Electrolysis ozone electrode and preparation method thereof and electrolysis ozone water die set
KR20130049031A (en) Germicidal sterilizer composition for hypochlrous acid solution and method for manufacturing sterilized water using the same
Qin et al. An experimental study of an NaClO generator for anti-microbial applications in the food industry
JP2004204328A (en) Method of producing hypochlorous acid solution, and utilizing method thereof
CN113693954B (en) Antibacterial hand sanitizer
CN113749982B (en) Preparation method of antibacterial hand sanitizer
CN113181096A (en) Plant extract no-clean hand sanitizer and preparation method thereof
CN113215596A (en) System suitable for industrial production hypochlorous acid sterilized water
CN109294750A (en) Antibacterial cleaning nanometer water of one kind and preparation method thereof
CN114959833B (en) Method for surface anodic oxidation antibacterial treatment of titanium and titanium alloy
WO2013144278A1 (en) Fluid based on water which is electrolytically treated in at least one electrolysis cell and use of the same as a cleaning and/or disinfection agent
KR20130049032A (en) Electrodes structure for high concentration hypochlrous acid solution from soidum chloride solution and method for manufacturing sterilized water using the same
CN111534387A (en) Cleaning agent and preparation method and application thereof
JP4147135B2 (en) Cleaning method for noodle cooking equipment
CN112956491A (en) Application of acidic electrolyzed oxidizing water in disinfection and sterilization of central kitchen environment
JP5073998B2 (en) How to improve silverware
JP4009385B2 (en) Degreasing cleaning method for metal articles

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
TA01 Transfer of patent application right
TA01 Transfer of patent application right

Effective date of registration: 20240124

Address after: No.10, Huimin 1st Road, No.6 Industrial Zone, Guanlan street, Longhua District, Shenzhen, Guangdong 518000

Applicant after: SWASHES PRODUCTS CO.,LTD.

Country or region after: China

Address before: College of chemistry and material engineering Jiangnan University No. 1800 214122 Jiangsu city of Wuxi Province Li Lake Avenue

Applicant before: Liang Lianzhi

Country or region before: China

GR01 Patent grant
GR01 Patent grant