CN110354296A - A kind of super water absorbent quick-drying paper diaper - Google Patents
A kind of super water absorbent quick-drying paper diaper Download PDFInfo
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- CN110354296A CN110354296A CN201910502896.6A CN201910502896A CN110354296A CN 110354296 A CN110354296 A CN 110354296A CN 201910502896 A CN201910502896 A CN 201910502896A CN 110354296 A CN110354296 A CN 110354296A
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- paper diaper
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
- A61F13/51—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
- A61F13/511—Topsheet, i.e. the permeable cover or layer facing the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
- A61F13/51—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
- A61F13/511—Topsheet, i.e. the permeable cover or layer facing the skin
- A61F13/512—Topsheet, i.e. the permeable cover or layer facing the skin characterised by its apertures, e.g. perforations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
- A61L15/24—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/425—Porous materials, e.g. foams or sponges
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
- C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
- A61F13/51—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
- A61F13/511—Topsheet, i.e. the permeable cover or layer facing the skin
- A61F13/51121—Topsheet, i.e. the permeable cover or layer facing the skin characterised by the material
- A61F2013/51147—Topsheet, i.e. the permeable cover or layer facing the skin characterised by the material being polymeric films
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
- A61F13/51—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
- A61F13/511—Topsheet, i.e. the permeable cover or layer facing the skin
- A61F13/513—Topsheet, i.e. the permeable cover or layer facing the skin characterised by its function or properties, e.g. stretchability, breathability, rewet, visual effect; having areas of different permeability
- A61F2013/51355—Topsheet, i.e. the permeable cover or layer facing the skin characterised by its function or properties, e.g. stretchability, breathability, rewet, visual effect; having areas of different permeability for improving fluid flow
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2351/00—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2471/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
- C08J2471/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
- C08K7/26—Silicon- containing compounds
Abstract
The present invention relates to new function material technical fields, disclose a kind of super water absorbent quick-drying paper diaper, human skin is contacted in diaper body covers one layer of super absorbent polymer membrane material on one side, porous adsorbent is prepared using hydration reaction method, large amount of adsorption, breathable moisture permeability is good, Material synthesis prepares high adsorption rapid-curing cutback precursor product based on polyacrylate dispersion, organic reactant is added again to dissolve each other, then porous adsorbent is added, carry out film formation reaction, the molding super absorbent polymer membrane material being prepared, it is at low cost that this method prepares superabsorbent water paper diaper, properties of product are prominent, the paper diaper core material structure of formation be fine and close hydration at, water absorbing capacity with super strength, mechanical strength is high, it is dry and comfortable to be able to maintain skin surface, the breeding of bacterium can also be inhibited to adhere to, it is formed immediately on surface after absorbing urine Physical gel prevents the reverse osmosis of urine.
Description
Technical field
The invention belongs to new function material technical fields, and in particular to a kind of super water absorbent quick-drying paper diaper.
Background technique
The user group of paper diaper mainly has baby and adult's two major classes.Wherein Chinese market is mainly baby's paper urine
Trousers, China have nearly 20,000,000 baby due every year, reach more than 4,000 ten thousand using 0 years old to 2 years old baby of urine pants.And according to state
The data of statistics bureau, family, 60 years old or more the population in the whole nation in 2008 reach 1.599 hundred million people, account for the 12% of total population;Over-65s it is old
Year population reaches 1.096 hundred million people account for total population 8.3%.
Diaper rash is the stimulation of mixture and cloth diaper (or paper diaper of poor quality) to skin because of urine and stool
With inflammation caused by friction, all occurs micro- red phenomenon from private parts to buttocks, skin can become coarse, or even occur superfine small
Acne.If the small long prickly heat of hip, while could also cause diaper using air-locked cloth diaper or the paper diaper of poor quality again
Rash.
As the promotion of living standard and science and technology strength develops, it is impossible to meet people for traditional diaper and paper diaper
Demand, the market competition of paper diaper is also more fierce.And to the promotion of paper diaper product nothing more than from use feeling and
Health environment-friendly angle is set out.Since paper diaper are directly contacted with human skin, the environment in urine is suitble to bacterial growth breeding, grows
Raw bacterium can be adsorbed on paper diaper surface, and then be adhered to skin, and the continuous breeding of bacterium is caused to accumulate.Existing paper diaper
The adsorbent material used either plant processing extract component or polymer adsorbing material, adsorption capacity is extremely limited, is easy
It bursts, and does not all have anti-reflective osmosis, absorption speed is slow, causes urine to contact for a long time with skin, antibacterial effect obtains not
To effective guarantee.It is easy to cause uncomfortable and infection, therefore it provides a kind of super water absorbent quick-drying paper diaper have highly important meaning
Justice.
Summary of the invention
The purpose of the present invention is being directed to existing problem, a kind of super water absorbent quick-drying paper diaper, the paper diaper of formation are provided
Core material structure is fine and close hydration at water absorbing capacity with super strength keeps skin surface dry and comfortable, additionally it is possible to inhibit bacterium
Adherency.
The present invention is achieved by the following technical solutions:
A kind of super water absorbent quick-drying paper diaper, human skin is contacted in diaper body covers one layer of super absorbent polymer on one side
Membrane material, the preparation of the super absorbent polymer membrane material the following steps are included:
(1) 15-18 milliliters of solder(ing)acids are measured, is added in beaker, 6-8 milliliters of sodium metasilicate water is slowly added dropwise into beaker
Solution, magnetic agitation mix 60-70 minutes, 1.4-1.5 grams of carbon dust are then added into mixture, while being added 30-35 milliliters
Ethylene glycol ultrasonic disperse 20-25 minutes, is added dropwise acetic acid regulation system pH value between 5.5-5.8, is then transferred to reaction kettle
In, insulation reaction temperature is set as 220-230 DEG C, the reaction time is 14-16 hours, after reaction cooled to room temperature,
It is small to be subsequently placed in 80-90 DEG C of baking oven dry 10-12 using deionized water and dehydrated alcohol alternately washing 3-5 times for reaction product
When, it pulverizes to obtain porous adsorbent;
(2) it weighs 180-190 grams of polyacrylate dispersion to be placed in a beaker with 15-16 grams of trimethoxy silane, 80-90 milli is added
Dehydrated alcohol is risen, places the beaker and is stirred 40-50 minutes on magnetic stirring apparatus with 350-400 revs/min of speed, dispersed
Uniform mixture is transferred in round-bottomed flask, and 35-40 milliliters of ethyl acrylates and 10-15 milli are at the uniform velocity sequentially added into flask
Triethylamine is risen, stirring 30-40 minutes is continued, heating water bath is stirred to react 0.5-0.6 hours to 80-85 DEG C, obtains precipitating mixing
Object is filtered, and obtains filtrate and set to be evaporated using Rotary Evaporators in a round bottom flask, residual solvent is removed, before obtaining
Drive body product;
(3) precursor product that step (2) is prepared is mixed with 110-120 milliliters of ethyl acetate, is added 100-110 milliliters
The porous adsorbent that step (1) is prepared, ultrasound point is added using 50-60 DEG C of hot water heating water bath in Aqueous Solutions of Polyethylene Glycol
It dissipates 30-40 minutes, dispersion is transferred in round-bottomed flask, is at the uniform velocity added dropwise to 4.0-5.0 milliliters of N, N- dimethyl under stiring
Formamide is persistently dispersed with stirring 20-30 minutes after dripping, and is passed through nitrogen and is reacted, and sets heating reaction temperature as 145-
150 DEG C, the reaction time is 1.5-2.0 hours, stands 3-4 hours after reaction, and it is molten that 20-25 milliliters of saturated sodium-chlorides are added
Liquid, concussion are cleaned, and are removed water phase after stratification, resultant product are added in Teflon mould, in 55-60 DEG C of vacuum
It is 10-12 hours dry in drying box, molding super absorbent polymer membrane material is obtained, was dried using soaked in absolute ethyl alcohol 4-5 hours
?.
It is further described as to above scheme, the super absorbent polymer membrane material covers with a thickness of 0.28-
0.30 millimeter.
It is further described as to above scheme, step (1) the solder(ing)acid mass concentration is 33-35%.
It is further described as to above scheme, step (1) the sodium silicate aqueous solution mass concentration is 25-30%.
It is further described as to above scheme, step (1) the porous adsorbent particle size is in 25-28 nanometer
Between.
It is further described as to above scheme, step (2) the polyacrylate dispersion mass concentration is 60-65%.
It is further described as to above scheme, step (3) the Aqueous Solutions of Polyethylene Glycol mass concentration is 45-50%.
It is further described as to above scheme, step (3) saturated sodium chloride solution is the saturated mode at 25 DEG C.
It is further described as to above scheme, diaper body is by non-woven fabrics outer layer, high molecular material water suction internal layer
It is formed with flexible cotton air-permeable layer.
The present invention has the advantage that solve the water-absorbent material adsorption capacity that existing paper diaper use compared with prior art
It is extremely limited, and do not have anti-reflective osmosis, the problem of antibacterial effect cannot get effective guarantee, it is super that the present invention provides one kind
Water absorbent quick-drying paper diaper, human skin is contacted in diaper body covers one layer of super absorbent polymer membrane material, benefit on one side
Porous adsorbent is prepared with hydration reaction method, large amount of adsorption, breathable moisture permeability is good, and raw material closes based on polyacrylate dispersion
It at preparing high adsorption rapid-curing cutback precursor product, then adds organic reactant and dissolves each other, porous adsorbent is then added, forms a film
Reaction, the molding super absorbent polymer membrane material being prepared, this method preparation superabsorbent water paper diaper are at low cost, properties of product are prominent
Out, the characteristics of super absorbent polymer membrane material is that aperture rate is high, water absorbing capacity is superpower, skin-friendly is good, stability is good, elasticity
Well, reverse osmosis ability is strong, which has performance well, the paper diaper of formation using upper in paper diaper
Core material structure is fine and close hydration at water absorbing capacity with super strength, mechanical strength is high, and it is dry to be able to maintain skin surface
It is refreshing, additionally it is possible to inhibit the breeding of bacterium to adhere to, manage gel in surface formation immediately after absorbing urine, prevent the reverse osmosis of urine
Thoroughly, the super water absorbent quick-drying paper diaper that the present invention uses, which solve the water-absorbent material adsorption capacity that existing paper diaper use, extremely to be had
Limit, and do not have anti-reflective osmosis, the problem of antibacterial effect cannot get effective guarantee, preparation cost is low, Yi Shixian scale
Production overcomes the short slab for the paper diaper water suction material that existing method is prepared, provides for the development and utilization of water-absorbent material
New thinking and direction, improves the development and utilization of high-end adsorbent material, can be realized and promotes high-quality paper diaper field industry
Development improves the realistic meaning in the application value of daily necessities field, is a kind of technical solution being extremely worth of widely use.
Specific embodiment
To make the purpose of the present invention, technical solution and effect clearer, clear and definite, combined with specific embodiments below to this hair
It is bright to be described further, it should be understood that the specific embodiments described herein are merely illustrative of the present invention, is not used to limit
Technical solution provided by the present invention.
Embodiment 1
A kind of super water absorbent quick-drying paper diaper, human skin is contacted in diaper body covers one layer of super absorbent polymer on one side
Membrane material, the preparation of the super absorbent polymer membrane material the following steps are included:
(1) 15 milliliters of solder(ing)acids are measured, is added in beaker, 6 milliliters of sodium silicate aqueous solutions is slowly added dropwise into beaker,
Magnetic agitation mixes 60 minutes, 1.4 grams of carbon dusts is then added into mixture, while 30 milliliters of ethylene glycol, ultrasonic disperse is added
20 minutes, acetic acid regulation system pH value is added dropwise between 5.5-5.8, is then transferred in reaction kettle, sets insulation reaction temperature
It is 220 DEG C, the reaction time is 14 hours, cooled to room temperature after reaction, and reaction product uses deionized water and anhydrous
Ethyl alcohol alternately washing 3 times, are subsequently placed in drying 10 hours in 80 DEG C of baking ovens, pulverize to obtain porous adsorbent;
(2) 180 grams of polyacrylate dispersions are weighed to be placed in a beaker with 15 grams of trimethoxy silanes, 80 milliliters of anhydrous second are added
Alcohol is placed the beaker and is stirred 40 minutes on magnetic stirring apparatus with 350 revs/min of speed, is obtained finely dispersed mixture and is turned
It moves in round-bottomed flask, 35 milliliters of ethyl acrylates and 10 milliliters of triethylamines is at the uniform velocity sequentially added into flask, continue stirring 30
Minute, heating water bath is stirred to react 0.5 hour to 80 DEG C, obtains precipitation mixture, be filtered, obtain filtrate and be placed in round bottom
It is evaporated in flask using Rotary Evaporators, removes residual solvent, obtain precursor product;
(3) precursor product that step (2) is prepared is mixed with 110 milliliters of ethyl acetate, 100 milliliters of polyethylene glycol is added
The porous adsorbent that step (1) is prepared is added using 50 DEG C of hot water heating water baths in aqueous solution, ultrasonic disperse 30 minutes, will
Dispersion is transferred in round-bottomed flask, is at the uniform velocity added dropwise to 4.0 milliliters of n,N-Dimethylformamide under stiring, is continued after dripping
It is dispersed with stirring 20 minutes, is passed through nitrogen and is reacted, set heating reaction temperature as 145 DEG C, the reaction time is 1.5 hours, instead
3 hours are stood after answering, 20 milliliters of saturated sodium chloride solutions are added, concussion is cleaned, and removes water phase after stratification, will be remaining
Product is added in Teflon mould, 10 hours dry in 55 DEG C of vacuum ovens, obtains molding super absorbent polymer
Membrane material was dried using soaked in absolute ethyl alcohol 4 hours.
It is further described as to above scheme, the super absorbent polymer membrane material covers with a thickness of 0.28 milli
Rice.
It is further described as to above scheme, step (1) the solder(ing)acid mass concentration is 33%.
It is further described as to above scheme, step (1) the sodium silicate aqueous solution mass concentration is 25%.
It is further described as to above scheme, step (1) the porous adsorbent particle size is in 25-28 nanometer
Between.
It is further described as to above scheme, step (2) the polyacrylate dispersion mass concentration is 60%.
It is further described as to above scheme, step (3) the Aqueous Solutions of Polyethylene Glycol mass concentration is 45%.
It is further described as to above scheme, step (3) saturated sodium chloride solution is the saturated mode at 25 DEG C.
It is further described as to above scheme, diaper body is by non-woven fabrics outer layer, high molecular material water suction internal layer
It is formed with flexible cotton air-permeable layer.
Embodiment 2
A kind of super water absorbent quick-drying paper diaper, human skin is contacted in diaper body covers one layer of super absorbent polymer on one side
Membrane material, the preparation of the super absorbent polymer membrane material the following steps are included:
(1) 16 milliliters of solder(ing)acids are measured, is added in beaker, 7 milliliters of sodium silicate aqueous solutions is slowly added dropwise into beaker,
Magnetic agitation mixes 65 minutes, 1.45 grams of carbon dusts is then added into mixture, while 32 milliliters of ethylene glycol, ultrasonic disperse is added
22 minutes, acetic acid regulation system pH value is added dropwise between 5.5-5.8, is then transferred in reaction kettle, sets insulation reaction temperature
It is 225 DEG C, the reaction time is 15 hours, cooled to room temperature after reaction, and reaction product uses deionized water and anhydrous
Ethyl alcohol alternately washing 4 times, are subsequently placed in drying 11 hours in 85 DEG C of baking ovens, pulverize to obtain porous adsorbent;
(2) 185 grams of polyacrylate dispersions are weighed to be placed in a beaker with 15.5 grams of trimethoxy silanes, 85 milliliters of anhydrous second are added
Alcohol is placed the beaker and is stirred 45 minutes on magnetic stirring apparatus with 380 revs/min of speed, is obtained finely dispersed mixture and is turned
It moves in round-bottomed flask, 38 milliliters of ethyl acrylates and 13 milliliters of triethylamines is at the uniform velocity sequentially added into flask, continue stirring 35
Minute, heating water bath is stirred to react 0.55 hour to 82 DEG C, obtains precipitation mixture, be filtered, obtain filtrate and be placed in round bottom
It is evaporated in flask using Rotary Evaporators, removes residual solvent, obtain precursor product;
(3) precursor product that step (2) is prepared is mixed with 115 milliliters of ethyl acetate, 105 milliliters of polyethylene glycol is added
The porous adsorbent that step (1) is prepared is added using 55 DEG C of hot water heating water baths in aqueous solution, ultrasonic disperse 35 minutes, will
Dispersion is transferred in round-bottomed flask, is at the uniform velocity added dropwise to 4.5 milliliters of n,N-Dimethylformamide under stiring, is continued after dripping
It is dispersed with stirring 25 minutes, is passed through nitrogen and is reacted, set heating reaction temperature as 148 DEG C, the reaction time is 1.8 hours, instead
3.5 hours are stood after answering, 22 milliliters of saturated sodium chloride solutions are added, concussion is cleaned, and is removed water phase after stratification, will be remained
Remaining product is added in Teflon mould, 11 hours dry in 58 DEG C of vacuum ovens, obtains molding superabsorbent water polymerization
Object membrane material was dried using soaked in absolute ethyl alcohol 4.5 hours.
It is further described as to above scheme, the super absorbent polymer membrane material covers with a thickness of 0.29 milli
Rice.
It is further described as to above scheme, step (1) the solder(ing)acid mass concentration is 34%.
It is further described as to above scheme, step (1) the sodium silicate aqueous solution mass concentration is 28%.
It is further described as to above scheme, step (1) the porous adsorbent particle size is in 25-28 nanometer
Between.
It is further described as to above scheme, step (2) the polyacrylate dispersion mass concentration is 62%.
It is further described as to above scheme, step (3) the Aqueous Solutions of Polyethylene Glycol mass concentration is 48%.
It is further described as to above scheme, step (3) saturated sodium chloride solution is the saturated mode at 25 DEG C.
It is further described as to above scheme, diaper body is by non-woven fabrics outer layer, high molecular material water suction internal layer
It is formed with flexible cotton air-permeable layer.
Embodiment 3
A kind of super water absorbent quick-drying paper diaper, human skin is contacted in diaper body covers one layer of super absorbent polymer on one side
Membrane material, the preparation of the super absorbent polymer membrane material the following steps are included:
(1) 18 milliliters of solder(ing)acids are measured, is added in beaker, 8 milliliters of sodium silicate aqueous solutions is slowly added dropwise into beaker,
Magnetic agitation mixes 70 minutes, 1.5 grams of carbon dusts is then added into mixture, while 35 milliliters of ethylene glycol, ultrasonic disperse is added
25 minutes, acetic acid regulation system pH value is added dropwise between 5.5-5.8, is then transferred in reaction kettle, sets insulation reaction temperature
It is 230 DEG C, the reaction time is 16 hours, cooled to room temperature after reaction, and reaction product uses deionized water and anhydrous
Ethyl alcohol alternately washing 5 times, are subsequently placed in drying 12 hours in 90 DEG C of baking ovens, pulverize to obtain porous adsorbent;
(2) 190 grams of polyacrylate dispersions are weighed to be placed in a beaker with 16 grams of trimethoxy silanes, 90 milliliters of anhydrous second are added
Alcohol is placed the beaker and is stirred 50 minutes on magnetic stirring apparatus with 400 revs/min of speed, is obtained finely dispersed mixture and is turned
It moves in round-bottomed flask, 40 milliliters of ethyl acrylates and 15 milliliters of triethylamines is at the uniform velocity sequentially added into flask, continue stirring 40
Minute, heating water bath is stirred to react 0.6 hour to 85 DEG C, obtains precipitation mixture, be filtered, obtain filtrate and be placed in round bottom
It is evaporated in flask using Rotary Evaporators, removes residual solvent, obtain precursor product;
(3) precursor product that step (2) is prepared is mixed with 120 milliliters of ethyl acetate, 110 milliliters of polyethylene glycol is added
The porous adsorbent that step (1) is prepared is added using 60 DEG C of hot water heating water baths in aqueous solution, ultrasonic disperse 40 minutes, will
Dispersion is transferred in round-bottomed flask, is at the uniform velocity added dropwise to 5.0 milliliters of n,N-Dimethylformamide under stiring, is continued after dripping
It is dispersed with stirring 30 minutes, is passed through nitrogen and is reacted, set heating reaction temperature as 150 DEG C, the reaction time is 2.0 hours, instead
4 hours are stood after answering, 25 milliliters of saturated sodium chloride solutions are added, concussion is cleaned, and removes water phase after stratification, will be remaining
Product is added in Teflon mould, 12 hours dry in 60 DEG C of vacuum ovens, obtains molding super absorbent polymer
Membrane material was dried using soaked in absolute ethyl alcohol 5 hours.
It is further described as to above scheme, the super absorbent polymer membrane material covers with a thickness of 0.30 milli
Rice.
It is further described as to above scheme, step (1) the solder(ing)acid mass concentration is 35%.
It is further described as to above scheme, step (1) the sodium silicate aqueous solution mass concentration is 30%.
It is further described as to above scheme, step (1) the porous adsorbent particle size is in 25-28 nanometer
Between.
It is further described as to above scheme, step (2) the polyacrylate dispersion mass concentration is 65%.
It is further described as to above scheme, step (3) the Aqueous Solutions of Polyethylene Glycol mass concentration is 45-50%.
It is further described as to above scheme, step (3) saturated sodium chloride solution is the saturated mode at 25 DEG C.
It is further described as to above scheme, diaper body is by non-woven fabrics outer layer, high molecular material water suction internal layer
It is formed with flexible cotton air-permeable layer.
Comparative example 1
Difference with embodiment 1 is only that, in the preparation of super absorbent polymer membrane material, omits the system of step (1) described adsorbent
Standby addition, remaining is consistent.
Comparative example 2
Difference with embodiment 2 is only that, in the preparation of super absorbent polymer membrane material, it is water-soluble to omit step (1) described zinc chloride
The addition of liquid uses, remaining is consistent.
Comparative example 3
Difference with embodiment 3 is only that, in the preparation of super absorbent polymer membrane material, in step (1) described reaction kettle, setting is protected
Warm reaction temperature is 190 DEG C, and the reaction time is 20 hours, remaining is consistent.
Comparative example 4
Difference with embodiment 3 is only that, in the preparation of super absorbent polymer membrane material, omits step (2) described trimethoxy silicon
The addition of alkane, remaining is consistent.
Comparative example 5
Difference with embodiment 3 is only that in the preparation of super absorbent polymer membrane material, step (3) the heating reaction temperature is
120 DEG C, the reaction time is 4.0 hours, remaining is consistent.
Comparative experiments
Super water absorbent quick-drying paper diaper are prepared using the method for embodiment 1-3 and comparative example 1-5 respectively.It is with patent publication No.
A kind of method that the paper diaper of good water absorption are related to disclosed in CN208677741U as a control group, under the same test conditions
Each group paper diaper sample is tested for the property, when data reach stable, acquires representative data, obtained experimental data
It for the average value of 5 groups of samples, keeps in test that irrelevant variable is consistent, counts effective average value and (utilize statistical method before experiment
Experimental design is carried out, test data is then tested and recorded, analysis obtains test result, makes full use of statistics in the process
Tool explains result to the greatest extent), as a result as shown in the table:
Project | Air permeability (ml/min) | Vapor transfer rate (g/scm2) | Bacteriostasis rate (%) | The porosity (%) |
Embodiment 1 | 105 | 9.6 | 99.8 | 72.3 |
Embodiment 2 | 105 | 9.8 | 99.9 | 72.4 |
Embodiment 3 | 105 | 9.7 | 99.8 | 72.3 |
Comparative example 1 | 102 | 4.9 | 75.6 | 45.3 |
Comparative example 2 | 103 | 5.6 | 80.8 | 55.8 |
Comparative example 3 | 104 | 8.8 | 86.3 | 61.4 |
Comparative example 4 | 103 | 6.7 | 82.6 | 56.2 |
Comparative example 5 | 104 | 8.2 | 88.9 | 63.7 |
Control group | 102 | 5.3 | 63.2 | 44.5 |
(air permeability test is measured using Ge Erlaifa air permeability instrument;The measurement of wet guilding: it is carried out according to national standard GB/T12704-91
Test, using the computermatic fabric moisture transmission instrument of YG601-II, using vapor transfer rate as deliberated index;Antibiotic property uses GB/T 20944.3-
2008 " the evaluation succusions of antibacterial textile performance " are tested: in this antibacterial experiment, reagent mainly has PBS buffer solution, meat
Soup and culture medium.After related medicine allocation, buffer PBS is divided in 2 5OO milliliters of conical flask, and meat soup,
Culture medium is completely dissolved ingredient after being both needed to heating, and selected strain is Escherichia coli;)
The super water absorbent quick-drying paper diaper that the present invention uses, which solve the water-absorbent material adsorption capacity that existing paper diaper use, extremely to be had
Limit, and do not have anti-reflective osmosis, the problem of antibacterial effect cannot get effective guarantee, preparation cost is low, Yi Shixian scale
Production overcomes the short slab for the paper diaper water suction material that existing method is prepared, provides for the development and utilization of water-absorbent material
New thinking and direction, improves the development and utilization of high-end adsorbent material, can be realized and promotes high-quality paper diaper field industry
Development improves the realistic meaning in the application value of daily necessities field, is a kind of technical solution being extremely worth of widely use.
Claims (9)
1. a kind of super water absorbent quick-drying paper diaper, which is characterized in that contact human skin in diaper body covers one on one side
Layer super absorbent polymer membrane material, the preparation of the super absorbent polymer membrane material the following steps are included:
(1) 15-18 milliliters of solder(ing)acids are measured, is added in beaker, 6-8 milliliters of sodium metasilicate water is slowly added dropwise into beaker
Solution, magnetic agitation mix 60-70 minutes, 1.4-1.5 grams of carbon dust are then added into mixture, while being added 30-35 milliliters
Ethylene glycol ultrasonic disperse 20-25 minutes, is added dropwise acetic acid regulation system pH value between 5.5-5.8, is then transferred to reaction kettle
In, insulation reaction temperature is set as 220-230 DEG C, the reaction time is 14-16 hours, after reaction cooled to room temperature,
It is small to be subsequently placed in 80-90 DEG C of baking oven dry 10-12 using deionized water and dehydrated alcohol alternately washing 3-5 times for reaction product
When, it pulverizes to obtain porous adsorbent;
(2) it weighs 180-190 grams of polyacrylate dispersion to be placed in a beaker with 15-16 grams of trimethoxy silane, 80-90 milli is added
Dehydrated alcohol is risen, places the beaker and is stirred 40-50 minutes on magnetic stirring apparatus with 350-400 revs/min of speed, dispersed
Uniform mixture is transferred in round-bottomed flask, and 35-40 milliliters of ethyl acrylates and 10-15 milli are at the uniform velocity sequentially added into flask
Triethylamine is risen, stirring 30-40 minutes is continued, heating water bath is stirred to react 0.5-0.6 hours to 80-85 DEG C, obtains precipitating mixing
Object is filtered, and obtains filtrate and set to be evaporated using Rotary Evaporators in a round bottom flask, residual solvent is removed, before obtaining
Drive body product;
(3) precursor product that step (2) is prepared is mixed with 110-120 milliliters of ethyl acetate, is added 100-110 milliliters
The porous adsorbent that step (1) is prepared, ultrasound point is added using 50-60 DEG C of hot water heating water bath in Aqueous Solutions of Polyethylene Glycol
It dissipates 30-40 minutes, dispersion is transferred in round-bottomed flask, is at the uniform velocity added dropwise to 4.0-5.0 milliliters of N, N- dimethyl under stiring
Formamide is persistently dispersed with stirring 20-30 minutes after dripping, and is passed through nitrogen and is reacted, and sets heating reaction temperature as 145-
150 DEG C, the reaction time is 1.5-2.0 hours, stands 3-4 hours after reaction, and it is molten that 20-25 milliliters of saturated sodium-chlorides are added
Liquid, concussion are cleaned, and are removed water phase after stratification, resultant product are added in Teflon mould, in 55-60 DEG C of vacuum
It is 10-12 hours dry in drying box, molding super absorbent polymer membrane material is obtained, was dried using soaked in absolute ethyl alcohol 4-5 hours
?.
2. a kind of super water absorbent quick-drying paper diaper as described in claim 1, which is characterized in that the super absorbent polymer membrane material
It covers with a thickness of 0.28-0.30 millimeters.
3. a kind of super water absorbent quick-drying paper diaper as described in claim 1, which is characterized in that step (1) described solder(ing)acid
Mass concentration is 33-35%.
4. a kind of super water absorbent quick-drying paper diaper as described in claim 1, which is characterized in that step (1) described sodium silicate aqueous solution
Mass concentration is 25-30%.
5. a kind of super water absorbent quick-drying paper diaper as described in claim 1, which is characterized in that step (1) the porous adsorbent grain
Diameter size is between 25-28 nanometers.
6. a kind of super water absorbent quick-drying paper diaper as described in claim 1, which is characterized in that step (2) the polyacrylate cream
Liquid mass concentration is 60-65%.
7. a kind of super water absorbent quick-drying paper diaper as described in claim 1, which is characterized in that step (3) described polyethylene glycol is water-soluble
Liquid mass concentration is 45-50%.
8. a kind of super water absorbent quick-drying paper diaper as described in claim 1, which is characterized in that step (3) described saturated sodium-chloride is molten
Liquid is the saturated mode at 25 DEG C.
9. a kind of super water absorbent quick-drying paper diaper as described in claim 1, which is characterized in that diaper body by non-woven fabrics outer layer,
High molecular material water suction internal layer and flexible cotton air-permeable layer composition.
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US11168287B2 (en) | 2016-05-26 | 2021-11-09 | Kimberly-Clark Worldwide, Inc. | Anti-adherent compositions and methods of inhibiting the adherence of microbes to a surface |
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US11168287B2 (en) | 2016-05-26 | 2021-11-09 | Kimberly-Clark Worldwide, Inc. | Anti-adherent compositions and methods of inhibiting the adherence of microbes to a surface |
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