CN113576764B - Preparation method of sanitary product absorption core - Google Patents

Preparation method of sanitary product absorption core Download PDF

Info

Publication number
CN113576764B
CN113576764B CN202111004771.4A CN202111004771A CN113576764B CN 113576764 B CN113576764 B CN 113576764B CN 202111004771 A CN202111004771 A CN 202111004771A CN 113576764 B CN113576764 B CN 113576764B
Authority
CN
China
Prior art keywords
layer
core body
absorption core
raw material
spraying
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
CN202111004771.4A
Other languages
Chinese (zh)
Other versions
CN113576764A (en
Inventor
吴晓彪
邱光益
林一速
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.)
Fujian Hengan Household Life Article Co Ltd
Original Assignee
Fujian Hengan Household Life Article 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 Fujian Hengan Household Life Article Co Ltd filed Critical Fujian Hengan Household Life Article Co Ltd
Priority to CN202111004771.4A priority Critical patent/CN113576764B/en
Publication of CN113576764A publication Critical patent/CN113576764A/en
Application granted granted Critical
Publication of CN113576764B publication Critical patent/CN113576764B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577Apparatus or processes for manufacturing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577Apparatus or processes for manufacturing
    • A61F13/15585Apparatus or processes for manufacturing of babies' napkins, e.g. diapers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577Apparatus or processes for manufacturing
    • A61F13/15764Transferring, feeding or handling devices; Drives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577Apparatus or processes for manufacturing
    • A61F13/15772Control
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577Apparatus or processes for manufacturing
    • A61F13/15804Plant, e.g. involving several steps
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/18Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing inorganic materials
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/24Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives thereof
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4382Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
    • D04H1/43825Composite fibres
    • D04H1/43828Composite fibres sheath-core
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4382Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
    • D04H1/43835Mixed fibres, e.g. at least two chemically different fibres or fibre blends
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577Apparatus or processes for manufacturing
    • A61F2013/15821Apparatus or processes for manufacturing characterized by the apparatus for manufacturing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577Apparatus or processes for manufacturing
    • A61F2013/15821Apparatus or processes for manufacturing characterized by the apparatus for manufacturing
    • A61F2013/15934Apparatus or processes for manufacturing characterized by the apparatus for manufacturing for making non-woven
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577Apparatus or processes for manufacturing
    • A61F2013/15821Apparatus or processes for manufacturing characterized by the apparatus for manufacturing
    • A61F2013/15934Apparatus or processes for manufacturing characterized by the apparatus for manufacturing for making non-woven
    • A61F2013/15967Apparatus or processes for manufacturing characterized by the apparatus for manufacturing for making non-woven by meltblown technique
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577Apparatus or processes for manufacturing
    • A61F2013/15821Apparatus or processes for manufacturing characterized by the apparatus for manufacturing
    • A61F2013/15934Apparatus or processes for manufacturing characterized by the apparatus for manufacturing for making non-woven
    • A61F2013/15991Apparatus or processes for manufacturing characterized by the apparatus for manufacturing for making non-woven in making composite multi-layered product
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F2013/16Sanitary towels; Means for supporting or fastening them

Abstract

The invention discloses a preparation method of an absorption core body of a hygienic product, wherein the absorption core body is prepared by spraying an acrylate foaming material prepared by a high internal phase emulsion method on a working table; the acrylic ester foaming material is formed by mixing a first raw material and a second raw material; the absorption core body is formed by spraying and stacking layer by utilizing a spray head with the same width as the absorption core body in the depth direction; wherein, the proportion of the first raw material and the second raw material in the sprayed acrylic ester foam material is continuously adjusted, so that the pore diameter of each layer of the absorption core body is gradually reduced from the middle to two sides in the length direction; and increasing the vacuum degree provided by the working table surface layer by layer in the spraying process so as to gradually reduce the pore diameter of the foam pores of the absorption core body in the depth direction from bottom to top or from top to bottom.

Description

Preparation method of sanitary product absorption core
Technical Field
The invention relates to a preparation method of an absorption core body of a hygienic product.
Background
The acrylic ester foaming material prepared by the high internal phase emulsion method is widely applied to the absorption core body of sanitary products (sanitary towels and paper diapers).
However, the absorbent cores produced by the prior art have the following drawbacks: the absorbent core is generally of a single-layer or double-layer structure, the control of the contradiction relation between the absorption speed and the back-permeation quantity is poor, the cell sizes are consistent in the length direction, and the liquid is not favorably diffused to two sides.
Disclosure of Invention
In order to overcome the defects, the invention provides a preparation method of a novel sanitary product absorption core body.
In order to achieve the aim, the invention provides a preparation method of an absorption core body of a hygienic product, wherein the absorption core body is prepared by spraying an acrylate foaming material prepared by a high internal phase emulsion method on a working table; the acrylate foaming material is formed by mixing a first raw material and a second raw material; the absorption core body is formed by spraying and stacking a spray head with the same width as the absorption core body layer by layer in the depth direction;
wherein, the proportion of the first raw material and the second raw material in the sprayed acrylic ester foam material is continuously adjusted, so that the pore diameter of each layer of the absorption core body is gradually reduced from the middle to two sides in the length direction; and increasing the vacuum degree provided by the working table surface layer by layer in the spraying process so as to gradually reduce the pore diameter of the foam pores of the absorption core body in the depth direction from bottom to top or from top to bottom.
Further, the method specifically comprises the following steps:
21) reading a preset value table, wherein the preset value table records the continuous change value of the ratio of the first raw material to the second raw material in each layer of the acrylate foaming material of the absorption core body along the length direction of the core body, the initial spraying amount of the corresponding spray head, the thickness value of each layer of the absorption core body and the vacuum degree of each layer;
22) spraying layer by layer according to a preset value table, and providing a preset vacuum degree through a working table;
23) monitoring whether the thickness of the current-layer absorption core body exceeds a preset threshold value in real time:
if the amount of the absorption core is over, the next layer is sprayed after the spraying amount of the next layer of the absorption core is proportionally reduced or increased;
if not, spraying the next layer according to the preset spraying amount;
24) whether the current layer is the last layer or not, if not, returning to the step 22);
if the last layer is selected, detecting whether the thickness of the current absorption core body exceeds a preset threshold value;
if the spraying amount of the spray head of the first layer of the next absorption core in the preset value table is exceeded, the spraying amount of the spray head of the first layer of the next absorption core in the preset value table is proportionally reduced or increased, and a new preset value table is formed; returning to step 21);
if the spraying amount of the spray head of each layer of the current absorption core body is not exceeded, recording the spraying amount of the spray head of each layer of the current absorption core body to form a new preset value table; return to step 21).
Further, the method specifically comprises the following steps:
31) reading a preset value table, wherein the preset value table records the proportion of a first raw material and a second raw material in each layer of acrylate foaming material of the absorption core body, the initial spraying amount of a corresponding spray head, the thickness value of each layer of the absorption core body and the vacuum degree of each layer;
32) spraying layer by layer according to a preset value table, and providing a preset vacuum degree through a working table;
33) monitoring whether the thickness of the current-layer absorption core body exceeds a preset threshold value in real time:
if the spraying amount of the next layer of the absorption core body is exceeded, the next layer is sprayed after the spraying amount of the next layer of the absorption core body is proportionally reduced or increased;
if not, spraying the next layer according to the preset spraying amount;
34) whether the current layer is the last layer, if not, returning to the step 32);
if the last layer is selected, detecting whether the thickness of the current absorption core body exceeds a preset threshold value;
if the spraying amount of the spray head of the first layer of the next absorption core in the preset value table is exceeded, the spraying amount of the spray head of the first layer of the next absorption core in the preset value table is proportionally reduced or increased, and a new preset value table is formed; returning to step 31);
if not: go to step 35);
35) detecting whether the weight of the current absorbent core exceeds a predetermined threshold;
if the weight of the current absorbing core body does not exceed the preset threshold value, recording the spraying amount of each layer of the current absorbing core body to form a new preset value table; returning to step 31);
if the weight of the current absorbing core body exceeds a preset threshold value, the mixing ratio and/or the spraying amount of the first raw material and the second raw material are increased or decreased according to a preset ratio, and a new preset value table is formed; returning to step 31.
The invention relates to a hygienic product, which comprises a surface layer and the absorption core body, wherein the surface layer is made of pure cotton non-woven fabric doped with 25-35% of moisture absorption fibers, and the moisture absorption fibers comprise a surface layer and a core layer; the skin layer is prepared from polyethylene, pore-forming materials and temperature-sensitive materials; the core layer is made of super absorbent resin or absorbent fibers;
wherein the micropores of the skin layer are in an open state at a temperature of above 33 ℃; the micropores of the skin layer are in a closed state at the temperature of below 33 ℃;
the moisture absorption fiber is prepared by adopting the following process:
70-90 parts of polyethylene, 0.5-3 parts of toughening agent, 1-5 parts of fluorine-containing acrylate resin, 0.5-3 parts of N-isopropyl acrylamide polymer and 10-30 parts of zinc oxide are mixed with 50-150 parts of core layer super absorbent resin material to prepare the moisture absorption fiber through spinning.
The pure cotton non-woven fabric needs to be subjected to after-treatment according to the following steps:
1) preparing an after-finishing agent;
2) adopting the prepared after-finishing agent to dip and prick the spunlace pure cotton non-woven fabric;
3) ionizing radiation grafting the soaked spunlace pure cotton non-woven fabric;
4) drying;
wherein the molecular formula of the after-finishing agent is as follows:
Figure BDA0003236813630000031
wherein R1 and R2 are higher fatty alcohol methacrylate ester or H, and the ester is cetyl ester or stearyl ester.
Adding trihydroxyethyl ethane, higher fatty alcohol methacrylate and fatty alcohol-polyoxyethylene ether into a composite emulsification system consisting of water, cetyl trimethyl ammonium bromide and tween 80, introducing nitrogen for protection, stirring at a constant temperature of 60-80 ℃, and adding an initiator (azodiisobutyronitrile and persulfate composite initiation system) to prepare the emulsion containing the system with the structural formula, wherein the emulsion contains polyhydric alcohol, higher fatty alcohol methacrylate water repellent groups and polyoxyethylene ether water repellent groups.
The absorption core body is formed by continuously spraying and stacking layer by layer in the depth direction by utilizing a spray head with the same width as the absorption core body, so that each layer of the absorption core body is continuous in the length direction; in the depth direction, in the continuous spraying process, due to the existence of vacuum provided by the working table, the pore diameter of each layer of absorption core body positioned below is larger than that positioned above; the ratio of the first raw material to the second raw material of the two adjacent layers of absorption cores and/or the vacuum degree corresponding to each layer of absorption core are adjusted, so that the pore diameter above the lower layer of absorption core in the two adjacent layers of absorption cores is the same as (or close to) the pore diameter below the upper layer of absorption core, and the interface between the two layers is eliminated; so that the aperture of the whole absorbing core body is gradually reduced from bottom to top along the depth direction.
Detailed Description
The invention aims to produce a multilayer absorption core body, wherein the absorption core body is prepared by spraying an acrylate foaming material prepared by a high internal phase emulsion method on a working table; the acrylic ester foaming material is formed by mixing a first raw material and a second raw material; the absorption core body is formed by spraying and stacking a spray head with the same width as the absorption core body layer by layer in the depth direction;
wherein, the proportion of the first raw material and the second raw material in the sprayed acrylic ester foam material is continuously adjusted, so that the pore diameter of each layer of the absorption core body is gradually reduced from the middle to two sides in the length direction; and increasing the vacuum degree provided by the working table surface layer by layer in the spraying process so as to gradually reduce the pore diameter of the foam pores of the absorption core body in the depth direction from bottom to top or from top to bottom.
The vacuum degree can be provided by a negative pressure fan or a vacuum device.
The spray head is a controlled spray head and is used for continuously adjusting the proportion and the spraying amount of the first raw material and the second raw material in the sprayed acrylic ester foaming material; the controlled spray head and the working platform move relatively to complete the spraying of each layer, the controlled spray head can be fixed, and the working platform moves relatively to the controlled spray head continuously; or the working platform can be fixed, and the controlled spray head continuously moves relative to the working platform. The working platform can be a flat plate type platform and is driven to reciprocate by a reciprocating driving device; or a die wheel, which is driven to rotate by a rotating device to realize relative motion.
In the production process, a system containing a low emulsifier can be mixed with the emulsifier by a double-screw extrusion mode, and the proportion of the emulsifier in the length direction of the high internal phase emulsion can be continuously regulated and controlled by continuously regulating and controlling the mixing proportion of the first raw material and the second raw material; then a layer of absorbing core body can be formed on the working table surface by continuously spraying the absorbing core body with a spray head with the same width as the absorbing core body according to a preset proportion value at a constant speed. When the absorption core is stacked layer by layer in the depth direction, the pore diameter of each layer of absorption core body positioned below is larger than the pore diameter of each layer of absorption core body positioned above due to the existence of vacuum provided by the working table; the ratio of the first raw material to the second raw material of the two adjacent layers of absorption cores and/or the vacuum degree corresponding to each layer of absorption core are adjusted, so that the pore diameter above the lower layer of absorption core in the two adjacent layers of absorption cores is the same as (or close to) the pore diameter below the upper layer of absorption core, and the interface between the two layers is eliminated; the pore diameter of the whole absorbing core body is gradually reduced from bottom to top along the depth direction (when in actual use, the pores are large and close to the surface layer of the sanitary product); the absorption core body with the structure between layers manufactured by the method has the following advantages: the pore diameter of the pores on the two sides is small, the capillary action is strong, the liquid can be absorbed towards the two sides, and the utilization rate of the absorption core body on the sanitary product is improved. The pore diameter of the lower layer of the foam pore is large, so that the foam pore can realize quick liquid infiltration when being used as an upper layer of an absorption core body and has low reverse osmosis; the pore diameter of the lower layer pores is small, so that the liquid can be quickly infiltrated when the lower layer is used as an absorption core body, and the high liquid retention capacity can be realized by utilizing the capillary action.
The raw materials of the acrylic ester foaming material comprise acrylic ester, a cross-linking agent, an initiator, an emulsifier and salt.
Wherein the acrylate is one or two of isooctyl acrylate and isooctyl methacrylate.
The cross-linking agent is ethylene glycol dimethacrylate, the emulsifier is Tween 80, the salt is calcium chloride, and the initiator is an oxidation-reduction initiation system and can be sodium persulfate, potassium persulfate, ammonium persulfate and the like.
The acrylate, the cross-linking agent, the initiator, the emulsifier and the water are emulsified by an emulsifying kettle to obtain stable emulsion as a first raw material. The second raw material is emulsifier Tween 80.
Usually, the amount of the cross-linking agent is 20-65% (wt, mass fraction, the same below) of the amount of the monomer, the amount of the initiator is 0.5-5% of the reactant, the amount of the emulsifier is 4-16% of the reactant, the emulsion concentration, i.e., the ratio of the water phase to the oil phase, is 10: 1-36: 1, and the emulsification temperature is 60-80 ℃.
As a further development of the invention, the absorbent core is produced by spraying on a die wheel: the die wheel is provided with an air vent communicated with vacuum equipment; a layer of polytetrafluoroethylene breathable film is coated on the die wheel corresponding to the air holes; the absorption core body is sprayed on the polytetrafluoroethylene breathable film, so that the finished absorption core body is favorably taken off from the die wheel; the absorbing core body can be sprayed one layer each time the absorbing core body rotates one circle, and a plurality of spray heads can be arranged above the peripheral side of the die wheel, and each spray head is sprayed one layer; in the spraying process of each layer, the vacuum equipment provides vacuum with preset vacuum degree for each absorption core body; thus, the absorption core body can be adsorbed on the die wheel by utilizing vacuum, which is beneficial to production; and adjusting the degree of vacuum as required can affect the thickness of each layer of the absorbent core, the formation of pores, and the like. For example, since the absorption core is sprayed layer by layer, under the condition of a certain vacuum degree, the vacuum has the largest influence on the absorption core in the spraying process of the lowest layer, and the influence is smaller as the absorption core goes upwards; meanwhile, due to the fact that the effect of the fan force on the polytetrafluoroethylene air-permeable membrane is different in different depth directions, the emulsion closer to the polytetrafluoroethylene air-permeable membrane has larger air volume and larger pore-forming size, and the pore diameter from the bottom to the top is gradually reduced. By combining with layer-by-layer accumulation, the aperture can be continuously changed in the depth direction and the adjustable range is large.
Example 1
The invention discloses a preparation method of an absorption core body of a hygienic product, which comprises the following steps:
the absorption core body is prepared by spraying an acrylate foaming material prepared by a high internal phase emulsion method on a working table; the acrylic ester foaming material is formed by mixing a first raw material and a second raw material; the absorption core body is formed by spraying and stacking layer by utilizing a spray head with the same width as the absorption core body in the depth direction;
wherein, the proportion of the first raw material and the second raw material in the sprayed acrylic ester foam material is continuously adjusted, so that the pore diameter of each layer of the absorption core body is gradually reduced from the middle to two sides in the length direction; and increasing the vacuum degree provided by the working table surface layer by layer in the spraying process so as to gradually reduce the pore diameter of the foam pores of the absorption core body in the depth direction from bottom to top or from top to bottom.
The method specifically comprises the following steps:
21) reading a preset value table, wherein the preset value table records the continuous change value of the ratio of the first raw material to the second raw material in each layer of the acrylate foaming material of the absorption core body along the length direction of the core body, the initial spraying amount of the corresponding spray head, the thickness value of each layer of the absorption core body and the vacuum degree of each layer;
22) spraying layer by layer according to a preset value table, and providing a preset vacuum degree through a working table;
23) monitoring in real time whether the thickness of the current-layer absorption core body exceeds a preset threshold value:
if the spraying amount of the next layer of the absorption core body is exceeded, the next layer is sprayed after the spraying amount of the next layer of the absorption core body is proportionally reduced or increased;
if not, spraying the next layer according to the preset spraying amount;
24) whether the current layer is the last layer or not, if not, returning to the step 22);
if the last layer is selected, detecting whether the thickness of the current absorption core body exceeds a preset threshold value;
if the spraying amount of the first layer of spray heads of the next absorption core in the preset value table is exceeded, the spraying amount of the first layer of spray heads of the next absorption core in the preset value table is proportionally reduced or increased, and a new preset value table is formed; returning to step 21);
if not, recording the spraying amount of each layer of the current absorption core body to form a new preset value table; return to step 21).
In this embodiment, the thickness of each layer is monitored to achieve product consistency.
Example 2
The embodiment is an improvement on the basis of embodiment 1, and the method specifically comprises the following steps:
31) reading a preset value table, wherein the preset value table records the continuous change value of the ratio of the first raw material to the second raw material in each layer of the acrylate foaming material of the absorption core body along the length direction of the core body, the initial spraying amount of the corresponding spray head, the thickness value of each layer of the absorption core body and the vacuum degree of each layer;
32) spraying layer by layer according to a preset value table, and providing a preset vacuum degree through a working table;
33) monitoring whether the thickness of the current-layer absorption core body exceeds a preset threshold value in real time:
if the spraying amount of the next layer of the absorption core body is exceeded, the next layer is sprayed after the spraying amount of the next layer of the absorption core body is proportionally reduced or increased;
if not, spraying the next layer according to the preset spraying amount;
34) whether the current layer is the last layer, if not, returning to the step 32);
if the last layer is selected, detecting whether the thickness of the current absorption core body exceeds a preset threshold value;
if the spraying amount of the first layer of spray heads of the next absorption core in the preset value table is exceeded, the spraying amount of the first layer of spray heads of the next absorption core in the preset value table is proportionally reduced or increased, and a new preset value table is formed; returning to step 31);
if not: go to step 35);
35) detecting whether the weight of the current absorbent core exceeds a predetermined threshold;
if the weight of the current absorption core body does not exceed the preset threshold value, recording the spraying amount of each layer of the current absorption core body to form a new preset value table; returning to step 31);
if the weight of the current absorbing core body exceeds a preset threshold value, the mixing ratio and/or the spraying amount of the first raw material and the second raw material are increased or decreased according to a preset ratio, and a new preset value table is formed; returning to step 31.
The weight of each absorbent core is taken into account in this embodiment. Considering that the foaming effect of the acrylic ester may be different due to different raw materials of each batch, the weight of the absorbent core is different under the condition of the same thickness of the absorbent core of different batches, and the consistency of the product is affected.
And (3) comparison test:
1. a sanitary napkin made of a foaming material is laid on a table, 10ml of pig blood is placed into the sanitary napkin by a pipette in alignment with a liquid adding point, timing is started, the time (namely, absorption time s) required after the absorption of the pig blood on the surface layer of the sanitary napkin is recorded, and the diffusion length (mm) of the blood on the surface layer is measured.
2. Weighing filter paper (diameter 110mm), and recording the weight of the filter paper as W1;
3. after 10min, a filter paper W1 with known weight is covered on the liquid adding point of the product, a 2.5kg briquetting (diameter 110mm) is placed, after 2min, the weight W2 of the filter paper is weighed, and the weight added by the filter paper (namely the rewet amount W) is calculated, and the formula is calculated: experimental results of W-W2-W1
Figure BDA0003236813630000071
Figure BDA0003236813630000081
Explanation of the phenomenon:
1. sample 1 has uniform pore diameter of small pores, and because the liquid is not easy to infiltrate downwards due to small pore diameter, the absorption time is long, but the capillary action of the small pores is strong, the liquid diffuses towards two sides, the diffusion length is longer, meanwhile, the strong capillary action has better liquid retention capacity, and the rewet capacity is lower.
2. The pore diameter of the big pore of the sample 2 is uniform, and the liquid quickly seeps downwards due to the large pore diameter, so the absorption speed is high, but the capillary action of the big pore is weak, the liquid is not easy to diffuse towards two sides, the diffusion length is short, and meanwhile, the liquid retention capacity is poor due to the weak capillary action, and the back seepage quantity is high.
3. The sample 3 has uniform cells in the length direction, large pore diameter of the upper layer of cells and small pore diameter of the lower layer of cells, and has the advantages and the disadvantages of the 1 st and the 2 nd, and each property is positioned in the middle of the two.
4. The pore diameter of the cells in the length direction of sample 4 is discontinuously reduced from the middle to both sides, the pore diameter of the upper layer of cells is large, the pore diameter of the lower layer of cells is small, the pore diameters of both sides are expected to be small, the pore diameter of the middle layer is large, and the liquid diffusion is improved, but the performance is poorer than that of sample 3, and presumably, the pore diameter of the cells in the length direction is discontinuous, so that an interface is formed, and the liquid diffusion and absorption are not facilitated.
5. Sample 5 length direction cell aperture reduces from the centre to both sides gradually, and upper strata cell aperture is big, and lower floor's cell aperture is little, for sample 3, 4, because the little capillary action on aperture on both sides is strong, the absorption rate is fast, and diffusion length is long, and the rewet volume is low.
6. In the invention, the pore diameter of the cells in the length direction of the sample 6 is gradually reduced from the middle to two sides, and the pore diameter of the cells in the depth direction is gradually reduced from top to bottom, so that a three-dimensional continuous absorption capillary diffusion effect is formed, and the absorption speed, the diffusion length and the rewet capacity are further improved relative to the performance of the sample 5.
The above embodiments can be applied to various types of diapers, sanitary napkins, etc., for example, the surface layer of the diaper is made of the above pure cotton nonwoven fabric.
The invention relates to a hygienic product, which comprises a surface layer and an absorption core body, wherein the surface layer is made of spunlace pure cotton non-woven fabric doped with 25-35% of moisture absorption fibers, and the moisture absorption fibers comprise a surface layer and a core layer; wherein, the skin layer is made of polyethylene, pore-forming material and temperature-sensitive material;
the core layer is made of super absorbent resin or absorbent fiber. Wherein, the micropores of the temperature sensitive material are in an open state at the temperature of more than 33 ℃; the micropores of the temperature-sensitive material are in a closed state at the temperature of below 33 ℃;
the moisture absorption fiber is prepared by adopting the following process:
70-90 parts of polyethylene, 0.5-3 parts of toughening agent, 1-5 parts of fluorine-containing acrylate resin, 0.5-3 parts of N-isopropyl acrylamide polymer and 10-30 parts of zinc oxide are mixed with 50-150 parts of core layer super absorbent resin material to prepare the moisture absorption fiber through spinning.
The moisture absorption fiber adopts a skin-core structure, and the skin layer zinc oxide is separated from the polyethylene base material part when the skin-core structure fiber is prepared and drafted, so that micropores are generated. But when the temperature is lower than 33 ℃, the N-isopropyl acrylamide polymer extends to block micropores; can absorb less moisture in the air. And the N-isopropyl acrylamide polymer shrinks at the temperature of more than 33 ℃ to open the micropores, and the generated micropores only allow water vapor to permeate but not allow water molecules to permeate, so that the super absorbent resin in the core layer is prevented from being saturated by urine, but can absorb the water vapor. The absorbent fibers in the core layer can absorb moisture in the area surrounded by the paper diaper, so that the surface of the paper diaper is kept dry.
The spunlace pure cotton non-woven fabric is subjected to after-treatment according to the following steps:
1) preparing an after-finishing agent;
2) adopting the prepared after finishing agent to dip and prick the spunlace pure cotton non-woven fabric;
3) ionizing radiation grafting the soaked spunlace pure cotton non-woven fabric;
4) drying;
wherein the molecular formula of the after-finishing agent is as follows:
Figure BDA0003236813630000101
wherein R1 and R2 are higher fatty alcohol methacrylate ester or H, and the ester is cetyl ester or stearyl ester.
The after-finishing agent is prepared by adding trihydroxyethyl ethane, higher fatty alcohol methacrylate and fatty alcohol-polyoxyethylene ether into a composite emulsifying system consisting of water, hexadecyl trimethyl ammonium bromide and tween 80, introducing nitrogen for protection, stirring at a constant temperature of 60-80 ℃, and adding an initiator (azodiisobutyronitrile and persulfate composite initiation system) to prepare the emulsion containing the system with the structural formula, wherein the emulsion contains polyalcohol, higher fatty alcohol methacrylate water repellent groups and polyoxyethylene ether hydrophilic groups.
Through the treatment, the hydroxyl of the polyhydric alcohol and the cellulose is crosslinked and grafted, the hydroxyl end group is sealed, the hydrophilicity is reduced, and meanwhile, the water repellent group, namely the higher aliphatic acrylate or the siloxane acrylate, forms a net to cover the surface of the cellulose, so that the hydrophilicity of the fiber is further reduced. Meanwhile, the polyoxyethylene ether group realizes the hydrophilic performance of the material and realizes the unification of the infiltration and the rewet of the liquid. Ionizing radiation is used for assisting, so that the hydroxyl hydrogen bonds of the cellulose fibers are depolymerized by the ionizing radiation, the structure is loose, and the activity of the cellulose is increased; p-toluenesulfonic acid is used as a catalyst, ionizing radiation is used as an initiating system, and hydroxyl is dehydrated and condensed into ether, so that the finishing agent system is fixed on the cellulose fiber.

Claims (1)

1. The preparation method of the sanitary product absorption core body is characterized in that the absorption core body is prepared by spraying an acrylate foaming material prepared by a high internal phase emulsion method on a working table; the acrylic ester foaming material is formed by mixing a first raw material and a second raw material; wherein, the first raw material is a system containing low emulsifier, and the second raw material is emulsifier; the absorbing core body is formed by spraying and stacking a spray head with the same width as the absorbing core body layer by layer in the depth direction;
wherein, the proportion of the first raw material and the second raw material in the sprayed acrylic ester foam material is continuously adjusted, so that the pore diameter of each layer of the absorption core body is gradually reduced from the middle to two sides in the length direction; and increasing the vacuum degree provided by the working table top layer by layer in the spraying process so as to gradually reduce the pore diameter of the foam pores of the absorption core body in the depth direction from bottom to top or from top to bottom;
the method specifically comprises the following steps:
1) reading a preset value table, wherein the preset value table records the proportion of a first raw material and a second raw material in each layer of acrylate foaming material of the absorption core body, the initial spraying amount of a corresponding spray head, the thickness value of each layer of the absorption core body and the vacuum degree of each layer;
2) spraying layer by layer according to a preset value table, and providing a preset vacuum degree through a working table;
3) monitoring whether the thickness of the current-layer absorption core body exceeds a preset threshold value in real time:
if the spraying amount of the next layer of the absorption core body is exceeded, the next layer is sprayed after the spraying amount of the next layer of the absorption core body is proportionally reduced or increased;
if not, spraying the next layer according to the preset spraying amount;
4) whether the current layer is the last layer or not, if not, returning to the step 2);
if the last layer is selected, detecting whether the thickness of the current absorption core body exceeds a preset threshold value;
if the spraying amount of the spray head of the first layer of the next absorption core in the preset value table is exceeded, the spraying amount of the spray head of the first layer of the next absorption core in the preset value table is proportionally reduced or increased, and a new preset value table is formed; returning to the step 1);
if not: go to step 5);
5) detecting whether the weight of the current absorbent core exceeds a predetermined threshold;
if the weight of the current absorbing core body does not exceed the preset threshold value, recording the spraying amount of each layer of the current absorbing core body to form a new preset value table; returning to the step 1);
if the weight of the current absorbing core body exceeds a preset threshold value, the mixing ratio and/or the spraying amount of the first raw material and the second raw material are increased or decreased according to a preset ratio, and a new preset value table is formed; returning to the step 1;
the absorbent core is made by spraying on a die wheel: the die wheel is provided with an air vent communicated with vacuum equipment; a layer of polytetrafluoroethylene ventilated membrane is covered on the die wheel corresponding to the air holes; the absorption core body is sprayed on the polytetrafluoroethylene ventilated membrane; the absorption core body is sprayed one layer each time the absorption core body rotates one circle, or a plurality of spray heads are arranged above the peripheral side of the die wheel, and each spray head is sprayed one layer; during each layer spraying process, a vacuum apparatus supplies a vacuum of a predetermined degree to each absorbent core.
CN202111004771.4A 2021-08-30 2021-08-30 Preparation method of sanitary product absorption core Active CN113576764B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202111004771.4A CN113576764B (en) 2021-08-30 2021-08-30 Preparation method of sanitary product absorption core

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202111004771.4A CN113576764B (en) 2021-08-30 2021-08-30 Preparation method of sanitary product absorption core

Publications (2)

Publication Number Publication Date
CN113576764A CN113576764A (en) 2021-11-02
CN113576764B true CN113576764B (en) 2022-07-05

Family

ID=78240239

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202111004771.4A Active CN113576764B (en) 2021-08-30 2021-08-30 Preparation method of sanitary product absorption core

Country Status (1)

Country Link
CN (1) CN113576764B (en)

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1217663A (en) * 1996-03-08 1999-05-26 普罗克特和甘保尔公司 Heterogeneous foam materials
CN104220240A (en) * 2012-03-30 2014-12-17 宝洁公司 Method of dewatering in a continuous high internal phase emulsion foam forming process
CN104311114A (en) * 2014-10-16 2015-01-28 中国科学院上海硅酸盐研究所 Method of preparing gradient porous silicon nitride ceramic material
CN106588073A (en) * 2015-10-20 2017-04-26 中国科学院上海硅酸盐研究所 Process for preparing novel laminated porous ceramic
CN109023209A (en) * 2018-09-21 2018-12-18 北京联合涂层技术有限公司 A kind of heat spraying method and system based on artificial intelligence
EP3711736A1 (en) * 2019-03-18 2020-09-23 Ontex BVBA Absorbent articles having an anisotropic foam acquisition layer
CN112676059A (en) * 2020-12-17 2021-04-20 江西五十铃汽车有限公司 Automobile paint checking method
CN112955262A (en) * 2018-11-30 2021-06-11 Abb瑞士股份有限公司 Coating of calibration objects

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110160321A1 (en) * 2009-12-30 2011-06-30 Steven Ray Merrigan Reduction of unpolymerized monomers in high internal phase emulsion foam

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1217663A (en) * 1996-03-08 1999-05-26 普罗克特和甘保尔公司 Heterogeneous foam materials
CN104220240A (en) * 2012-03-30 2014-12-17 宝洁公司 Method of dewatering in a continuous high internal phase emulsion foam forming process
CN104311114A (en) * 2014-10-16 2015-01-28 中国科学院上海硅酸盐研究所 Method of preparing gradient porous silicon nitride ceramic material
CN106588073A (en) * 2015-10-20 2017-04-26 中国科学院上海硅酸盐研究所 Process for preparing novel laminated porous ceramic
CN109023209A (en) * 2018-09-21 2018-12-18 北京联合涂层技术有限公司 A kind of heat spraying method and system based on artificial intelligence
CN112955262A (en) * 2018-11-30 2021-06-11 Abb瑞士股份有限公司 Coating of calibration objects
EP3711736A1 (en) * 2019-03-18 2020-09-23 Ontex BVBA Absorbent articles having an anisotropic foam acquisition layer
CN112676059A (en) * 2020-12-17 2021-04-20 江西五十铃汽车有限公司 Automobile paint checking method

Also Published As

Publication number Publication date
CN113576764A (en) 2021-11-02

Similar Documents

Publication Publication Date Title
EP0802928B1 (en) Use of polyglycerol aliphatic ether emulsifiers in making high internal phase emulsions that can be polymerized to provide absorbent foams
DE60129519T2 (en) Water-absorbing agent and process for its preparation
CA2208575C (en) Absorbent foams made from high internal phase emulsions useful for acquiring aqueous fluids
EP0802927B1 (en) Absorbent foams made from high internal phase emulsions useful for acquiring and distributing aqueous fluids
JP3288710B2 (en) Absorbent foams for aqueous fluids made from high internal phase emulsions with very high water to oil ratio
JP3432828B2 (en) Foams made from high internal phase emulsions useful as menstrual pad absorbent components
KR100283465B1 (en) Heterogeneous foam materials
JP3230582B2 (en) Absorbent foam material for aqueous bodily fluids that is thin until wet and method for producing the same
JPH08511724A (en) Absorber member with slits for aqueous bodily fluids formed of expandable absorbent material
WO1993004113A1 (en) Method for hydrophilizing absorbent foam materials
JPH10330519A (en) Foam material, its production and use, and absorbent disposable article containing such foam material
JP2004001355A (en) Absorber, absorbent article, water absorbent resin, and its manufacturing method and evaluating method
CN113693826B (en) Sanitary article
CN113576764B (en) Preparation method of sanitary product absorption core
CN113668249B (en) Sanitary article, pure cotton non-woven fabric, and method for producing pure cotton non-woven fabric
CN1852692A (en) Absorptive article
CN108004793B (en) Disposable absorbent product using graphene non-woven fabric
KR101800085B1 (en) Moisture superabsorbent composition using solvent type polyurethane and moisture absorbing fiber based textile using the compostion and a method thereof
KR20240041706A (en) Absorbent sheet, method for manufacturing same, and absorbent article comprising same
JPH02153731A (en) Moisture absorbing sheet
AU5714299A (en) Process for preparation of absorbent foam materials
MXPA97005237A (en) Absorbent foams made from high internal phase emulsions useful for acquiring aqueous fluids

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant