CN118022035B - Memory core and preparation method and application thereof - Google Patents
Memory core and preparation method and application thereof Download PDFInfo
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- CN118022035B CN118022035B CN202410118652.9A CN202410118652A CN118022035B CN 118022035 B CN118022035 B CN 118022035B CN 202410118652 A CN202410118652 A CN 202410118652A CN 118022035 B CN118022035 B CN 118022035B
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- 238000002360 preparation method Methods 0.000 title abstract description 23
- 239000000835 fiber Substances 0.000 claims abstract description 157
- 229920001131 Pulp (paper) Polymers 0.000 claims abstract description 105
- 239000002131 composite material Substances 0.000 claims abstract description 46
- 239000011347 resin Substances 0.000 claims abstract description 44
- 229920005989 resin Polymers 0.000 claims abstract description 44
- 239000002250 absorbent Substances 0.000 claims abstract description 34
- 239000002344 surface layer Substances 0.000 claims abstract description 15
- 239000012792 core layer Substances 0.000 claims abstract description 14
- 238000002844 melting Methods 0.000 claims abstract description 10
- 230000008018 melting Effects 0.000 claims abstract description 10
- 239000002861 polymer material Substances 0.000 claims abstract description 10
- 239000002994 raw material Substances 0.000 claims abstract description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 30
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 25
- 229920000768 polyamine Polymers 0.000 claims description 24
- 238000006243 chemical reaction Methods 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 23
- 239000004593 Epoxy Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 17
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 16
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical compound [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 claims description 16
- -1 polypropylene Polymers 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 9
- 230000008569 process Effects 0.000 claims description 7
- 239000003999 initiator Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 5
- 238000001914 filtration Methods 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 229920000573 polyethylene Polymers 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 4
- 230000035515 penetration Effects 0.000 claims description 4
- 229920001155 polypropylene Polymers 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- GHWVXCQZPNWFRO-UHFFFAOYSA-N butane-2,3-diamine Chemical compound CC(N)C(C)N GHWVXCQZPNWFRO-UHFFFAOYSA-N 0.000 claims 1
- 230000002745 absorbent Effects 0.000 abstract description 19
- 239000000243 solution Substances 0.000 description 18
- 238000010521 absorption reaction Methods 0.000 description 15
- 239000007788 liquid Substances 0.000 description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 239000007822 coupling agent Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 230000004048 modification Effects 0.000 description 5
- 238000012986 modification Methods 0.000 description 5
- 239000004745 nonwoven fabric Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 230000006835 compression Effects 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 4
- 239000004831 Hot glue Substances 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 210000004369 blood Anatomy 0.000 description 3
- QVYARBLCAHCSFJ-UHFFFAOYSA-N butane-1,1-diamine Chemical compound CCCC(N)N QVYARBLCAHCSFJ-UHFFFAOYSA-N 0.000 description 3
- 239000000805 composite resin Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 230000002175 menstrual effect Effects 0.000 description 3
- 239000008267 milk Substances 0.000 description 3
- 210000004080 milk Anatomy 0.000 description 3
- 235000013336 milk Nutrition 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
Classifications
-
- 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
- A61F13/15577—Apparatus or processes for manufacturing
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47K—SANITARY EQUIPMENT NOT OTHERWISE PROVIDED FOR; TOILET ACCESSORIES
- A47K10/00—Body-drying implements; Toilet paper; Holders therefor
- A47K10/16—Paper towels; Toilet paper; Holders therefor
-
- 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
- A61F13/15577—Apparatus or processes for manufacturing
- A61F13/15617—Making absorbent pads from fibres or pulverulent material with or without treatment of the fibres
-
- 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
- A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
- A61L15/26—Macromolecular compounds obtained otherwise than 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
- A61L15/40—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing ingredients of undetermined constitution or reaction products thereof, e.g. plant or animal extracts
-
- 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
-
- 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
- A61F2013/16—Sanitary towels; Means for supporting or fastening them
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Materials Engineering (AREA)
- Hematology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing & Machinery (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Botany (AREA)
- Zoology (AREA)
- Nonwoven Fabrics (AREA)
- Absorbent Articles And Supports Therefor (AREA)
Abstract
Description
技术领域Technical Field
本申请涉及吸收芯体领域,尤其是涉及一种记忆芯体及其制备方法及应用。The present application relates to the field of absorbent cores, and in particular to a memory core and a preparation method and application thereof.
背景技术Background Art
吸收芯体常用于卫生用品,例如纸尿裤和卫生巾,具有吸液和储液的功能,因此在卫生用品中的地位极其重要。Absorbent cores are often used in sanitary products, such as diapers and sanitary napkins. They have the functions of absorbing and storing liquid, so they play an extremely important role in sanitary products.
吸收芯体的分类包括木浆芯体和复合芯体,其中木浆芯体由木浆纤维和吸水树脂组成,特点是快速吸液,但存在易起坨的缺点;复合芯体采用多层无纺布搭配热熔胶压合吸水树脂而成,无纺布限制吸水树脂的移动,从而使得复合芯体平整不易起坨。The classification of absorbent cores includes wood pulp cores and composite cores. The wood pulp core is composed of wood pulp fibers and absorbent resins, and is characterized by rapid liquid absorption, but has the disadvantage of being prone to clumping. The composite core is made of multiple layers of non-woven fabrics and hot-melt adhesive pressed together with absorbent resins. The non-woven fabrics limit the movement of the absorbent resins, making the composite core smooth and less prone to clumping.
然而也是由于无纺布和热熔胶的原因,使得复合芯体整体质感较硬,缺乏弹性,导致芯体受挤压后不能及时恢复形状,降低了使用者在穿戴卫生用品时的体验。However, due to the non-woven fabric and hot-melt adhesive, the overall texture of the composite core is relatively hard and lacks elasticity, resulting in the core being unable to recover its shape in time after being squeezed, reducing the user's experience when wearing sanitary products.
发明内容Summary of the invention
为了提高吸收芯体的弹性,改善穿戴吸收芯体时的舒适感,本申请提供一种记忆芯体及其制备方法及应用。In order to increase the elasticity of the absorbent core and improve the comfort when wearing the absorbent core, the present application provides a memory core and a preparation method and application thereof.
第一方面,本申请提供的一种记忆芯体采用如下的技术方案:In the first aspect, the present application provides a memory core adopting the following technical solution:
一种记忆芯体,由包括以下重量份的原料经热粘合制备而成:A memory core is prepared by thermal bonding of the following raw materials in parts by weight:
木浆纤维10~30份;10-30 parts of wood pulp fiber;
吸水树脂20~100份;20 to 100 parts of water-absorbing resin;
复合纤维3~15份;3-15 parts of composite fiber;
所述复合纤维包括芯层和表层,所述芯层和所述表层均由聚合物材料组成,所述芯层的聚合物材料的熔点高于所述表层的聚合物材料的熔点。The composite fiber comprises a core layer and a surface layer, wherein both the core layer and the surface layer are composed of a polymer material, and the melting point of the polymer material of the core layer is higher than the melting point of the polymer material of the surface layer.
通过采用上述技术方案,利用复合纤维的表层低熔点的特性,在热粘合的过程中,表层部分熔融软化,产生粘合力,使复合纤维与木浆纤维交织形成网络结构,芯层的高熔点特性为该网络结构提供强度和稳定性,并且复合纤维与木浆纤维交织也对分散于网络结构中的吸水树脂形成包围和支撑,提高吸水树脂的分散稳定性,保证芯体吸液能力的同时有效降低吸水树脂团聚、起坨的可能,从而改善芯体的平整性。另外由于结构稳定,无需无纺布等非织造材料作为芯体的基础,木浆纤维、吸水树脂和复合纤维形成的结构具有较高的弹性,使芯体受挤压后能够快速恢复原形,得到类似于记忆海绵的形变恢复功能,即得到记忆芯体。By adopting the above technical solution, the surface layer of the composite fiber is partially melted and softened during the thermal bonding process, generating bonding force, so that the composite fiber and the wood pulp fiber are interwoven to form a network structure, and the high melting point of the core layer provides strength and stability for the network structure, and the interweaving of the composite fiber and the wood pulp fiber also surrounds and supports the water-absorbing resin dispersed in the network structure, thereby improving the dispersion stability of the water-absorbing resin, ensuring the liquid absorption capacity of the core body, and effectively reducing the possibility of agglomeration and lumping of the water-absorbing resin, thereby improving the flatness of the core body. In addition, due to the stable structure, non-woven materials such as non-woven fabrics are not required as the basis of the core body. The structure formed by the wood pulp fiber, the water-absorbing resin and the composite fiber has high elasticity, so that the core body can quickly recover its original shape after being squeezed, and a deformation recovery function similar to that of memory sponge is obtained, that is, a memory core body is obtained.
可选的,所述芯层为聚丙烯材料或聚酯材料,所述表层为聚乙烯材料。Optionally, the core layer is made of polypropylene material or polyester material, and the surface layer is made of polyethylene material.
通过采用上述技术方案,聚丙烯和聚酯强度较高,且熔点高于聚乙烯,因此适合作为芯层材料,聚乙烯熔点较低,适合在热粘合过程中部分熔融软化,从而实现复合纤维之间的连接粘合以及复合纤维与木浆纤维、吸水树脂之间的连接粘合。By adopting the above technical scheme, polypropylene and polyester have higher strength and higher melting points than polyethylene, so they are suitable as core layer materials. Polyethylene has a lower melting point and is suitable for partial melting and softening during the thermal bonding process, thereby achieving connection and bonding between composite fibers and between composite fibers and wood pulp fibers and absorbent resins.
可选的,所述木浆纤维为改性木浆纤维,所述改性木浆纤维通过环氧基硅烷偶联剂和乙烯基硅烷偶联剂预处理木浆纤维,再进行丙烯腈和异戊二烯共聚接枝,然后进行多胺化合物接枝,得到改性木浆纤维。Optionally, the wood pulp fiber is a modified wood pulp fiber, which is obtained by pretreating the wood pulp fiber with an epoxy silane coupling agent and a vinyl silane coupling agent, copolymerizing and grafting acrylonitrile and isoprene, and then grafting a polyamine compound to obtain the modified wood pulp fiber.
通过采用上述技术方案,环氧基硅烷偶联剂和乙烯基硅烷偶联剂的预处理使得木浆纤维表面接入环氧基官能团和乙烯基官能团,其中乙烯基官能团可以为丙烯腈和异戊二烯的共聚接枝提供接入基础,使丙烯腈与异戊二烯的共聚物接枝于木浆纤维表面,由于丙烯腈与异戊二烯的共聚结构与复合纤维的聚烯烃结构有相似的部分,因此提高木浆纤维与复合纤维的相容性,分散性和粘合效果更好;环氧基官能团可以为多胺化合物的接枝提供接入基础,多胺可以与吸水树脂形成官能团键合,由此木浆纤维、吸水树脂和复合纤维形成强度更高的芯体,芯体内的导流通道更稳定,并且由于提高木浆纤维与吸水树脂的连接稳定性,因此吸液能力同样得到提高。By adopting the above technical scheme, the pretreatment of epoxy silane coupling agent and vinyl silane coupling agent allows the epoxy functional group and vinyl functional group to be connected to the surface of the wood pulp fiber, wherein the vinyl functional group can provide an access basis for the copolymerization grafting of acrylonitrile and isoprene, so that the copolymer of acrylonitrile and isoprene is grafted on the surface of the wood pulp fiber. Since the copolymer structure of acrylonitrile and isoprene has a similar part to the polyolefin structure of the composite fiber, the compatibility of the wood pulp fiber and the composite fiber is improved, and the dispersibility and bonding effect are better; the epoxy functional group can provide an access basis for the grafting of polyamine compounds, and the polyamine can form a functional group bond with the water-absorbent resin, thereby the wood pulp fiber, the water-absorbent resin and the composite fiber form a core with higher strength, and the guide channel in the core is more stable, and since the connection stability between the wood pulp fiber and the water-absorbent resin is improved, the liquid absorption capacity is also improved.
可选的,所述木浆纤维、环氧基硅烷偶联剂、乙烯基硅烷偶联剂、丙烯腈、异戊二烯和多胺化合物的质量比为10:(0.5~1):(0.5~1):(0.15~0.3):(0.2~0.4):(0.18~0.3)。Optionally, the mass ratio of the wood pulp fiber, epoxy silane coupling agent, vinyl silane coupling agent, acrylonitrile, isoprene and polyamine compound is 10:(0.5-1):(0.5-1):(0.15-0.3):(0.2-0.4):(0.18-0.3).
通过采用上述技术方案,控制环氧基硅烷偶联剂、乙烯基硅烷偶联剂、丙烯腈、异戊二烯和多胺化合物的加入比例,调节木浆纤维的表面接枝状态,从而更好的与复合纤维以及吸水树脂结合。By adopting the above technical scheme, the addition ratio of epoxy silane coupling agent, vinyl silane coupling agent, acrylonitrile, isoprene and polyamine compounds is controlled, and the surface grafting state of wood pulp fiber is adjusted, so as to better combine with composite fiber and water-absorbing resin.
可选的,所述多胺化合物为丁二胺和己二胺中的一种或两种。Optionally, the polyamine compound is one or both of butanediamine and hexamethylenediamine.
通过采用上述技术方案,丁二胺和己二胺具有较长的碳链,使木浆纤维与吸水树脂的键合结构更加合理,促进液体在芯体内流动,提高储液能力。By adopting the above technical solution, butanediamine and hexamethylenediamine have longer carbon chains, which makes the bonding structure between wood pulp fiber and water-absorbing resin more reasonable, promotes the flow of liquid in the core, and improves the liquid storage capacity.
可选的,所述吸水树脂为丙烯酸型吸水树脂。Optionally, the water-absorbing resin is an acrylic water-absorbing resin.
通过采用上述技术方案,吸水树脂中的丙烯酸与木浆纤维中的多胺化合物形成键合,提高木浆纤维与吸水树脂的连接稳定性。By adopting the above technical solution, the acrylic acid in the water-absorbing resin forms a bond with the polyamine compound in the wood pulp fiber, thereby improving the connection stability between the wood pulp fiber and the water-absorbing resin.
第二方面,本申请提供的一种记忆芯体的制备方法采用如下的技术方案:In a second aspect, the present application provides a method for preparing a memory core using the following technical solution:
一种记忆芯体的制备方法,包括以下步骤:A method for preparing a memory core comprises the following steps:
将木浆纤维和复合纤维混合,打散,气流成网,在气流成网的过程中加入吸水树脂,形成纤网,然后热粘合加固,再压实,冷却,得到记忆芯体。The wood pulp fiber and the composite fiber are mixed, broken up, and air-laid. During the air-laid process, a water-absorbent resin is added to form a fiber web, which is then thermally bonded and reinforced, compacted, and cooled to obtain a memory core.
通过采用上述技术方案,气流成网的方式使得木浆纤维和复合纤维分散均匀,因此加入吸水树脂后能够保证吸水树脂具有良好的分散性,提高芯体的平整性和弹性。By adopting the above technical solution, the wood pulp fibers and composite fibers are evenly dispersed in the air-laid manner, so after adding the water-absorbent resin, the water-absorbent resin can be ensured to have good dispersion, thereby improving the flatness and elasticity of the core.
可选的,热粘合采用热风穿透的方式,热风温度为120~140℃。Optionally, the thermal bonding is performed by hot air penetration, and the hot air temperature is 120-140°C.
通过采用上述技术方案,热风穿透的方式促使复合纤维均匀受热,更好的发生熔融软化,从而产生粘合力,形成稳定性纤网。By adopting the above technical solution, the hot air penetration method causes the composite fibers to be heated evenly, melt and soften better, thereby generating bonding force and forming a stable fiber web.
可选的,将木浆纤维和复合纤维混合之前,还包括将木浆纤维粉碎和开松,将复合纤维开松。Optionally, before mixing the wood pulp fibers and the composite fibers, the process further includes crushing and loosening the wood pulp fibers and loosening the composite fibers.
通过采用上述技术方案,减少木浆纤维和复合纤维团聚的情况,促使木浆纤维和复合纤维混合均匀。By adopting the above technical solution, the agglomeration of wood pulp fibers and composite fibers is reduced, and the wood pulp fibers and composite fibers are mixed evenly.
可选的,形成纤网的步骤设置有多次,后一次步骤在前一次步骤所形成的纤网承载面上进行。Optionally, the step of forming the fiber web is performed multiple times, and a subsequent step is performed on the fiber web bearing surface formed in the previous step.
通过采用上述技术方案,纤网逐层铺叠,有利于吸水树脂在芯体中分散性的提高。By adopting the above technical solution, the fiber webs are stacked layer by layer, which is beneficial to improving the dispersion of the water-absorbing resin in the core.
可选的,所述改性木浆纤维的制备方法,包括以下步骤:Optionally, the method for preparing the modified wood pulp fiber comprises the following steps:
将木浆纤维分散于第一溶剂中,加入环氧基硅烷偶联剂和乙烯基硅烷偶联剂,加热反应,反应结束后过滤,得到第一木浆纤维;Dispersing wood pulp fibers in a first solvent, adding an epoxy silane coupling agent and a vinyl silane coupling agent, heating for reaction, and filtering after the reaction is completed to obtain first wood pulp fibers;
将第一木浆纤维分散于第二溶剂中,加入丙烯腈和异戊二烯,加热,缓慢加入引发剂,加入完毕后继续反应,反应结束后过滤,得到第二木浆纤维;The first wood pulp fiber is dispersed in the second solvent, acrylonitrile and isoprene are added, the mixture is heated, an initiator is slowly added, and the reaction is continued after the addition is completed. After the reaction is completed, the mixture is filtered to obtain the second wood pulp fiber;
将第二木浆纤维分散于第三溶剂中,加入多胺化合物,加热反应,反应结束后过滤,得到改性木浆纤维。The second wood pulp fiber is dispersed in the third solvent, a polyamine compound is added, and the mixture is heated for reaction. After the reaction is completed, the mixture is filtered to obtain the modified wood pulp fiber.
第三方面,本申请提供的一种记忆芯体的应用,包括在纸尿裤、卫生巾、哺乳吸奶巾、吸汗巾和厨房纸的应用。In a third aspect, the present application provides an application of a memory core, including applications in diapers, sanitary napkins, breastfeeding towels, sweat-absorbing towels and kitchen paper.
综上所述,本申请具有以下有益效果:In summary, this application has the following beneficial effects:
1、本申请利用复合纤维的表层低熔点的特性,在热粘合的过程中,表层部分熔融软化,产生粘合力,使复合纤维与木浆纤维交织形成网络结构,并且复合纤维与木浆纤维交织也对分散于网络结构中的吸水树脂形成包围和支撑,提高吸水树脂的分散稳定性,保证芯体吸液能力的同时有效降低吸水树脂团聚、起坨的可能,从而改善芯体的平整性。另外由于结构稳定,无需无纺布等非织造材料作为芯体的基础,木浆纤维、吸水树脂和复合纤维形成的结构具有较高的弹性,使芯体受挤压后能够快速恢复原形,得到类似于记忆海绵的形变恢复功能,即得到记忆芯体。1. The present application utilizes the low melting point of the surface layer of the composite fiber. During the thermal bonding process, the surface layer partially melts and softens, generating bonding force, so that the composite fiber and the wood pulp fiber are interwoven to form a network structure. The interweaving of the composite fiber and the wood pulp fiber also surrounds and supports the water-absorbing resin dispersed in the network structure, thereby improving the dispersion stability of the water-absorbing resin, ensuring the liquid absorption capacity of the core body while effectively reducing the possibility of the water-absorbing resin agglomerating and lumping, thereby improving the flatness of the core body. In addition, due to the stable structure, there is no need for non-woven materials such as non-woven fabrics as the basis of the core body. The structure formed by the wood pulp fiber, the water-absorbing resin and the composite fiber has high elasticity, so that the core body can quickly recover its original shape after being squeezed, and obtain a deformation recovery function similar to that of memory sponge, that is, a memory core body is obtained.
2、本申请还采用改性木浆纤维,提高木浆纤维与复合纤维的相容性,以及提高木浆纤维与吸水树脂的键合能力,由此木浆纤维、吸水树脂和复合纤维形成强度更高的芯体,芯体内的导流通道更稳定,并且由于提高木浆纤维与吸水树脂的连接稳定性,因此吸液能力同样得到提高。2. The present application also uses modified wood pulp fibers to improve the compatibility of wood pulp fibers and composite fibers, as well as the bonding ability of wood pulp fibers and water-absorbent resins. As a result, wood pulp fibers, water-absorbent resins and composite fibers form a core with higher strength, and the flow guide channels in the core are more stable. In addition, since the connection stability between wood pulp fibers and water-absorbent resins is improved, the liquid absorption capacity is also improved.
具体实施方式DETAILED DESCRIPTION
以下对本申请作进一步详细说明。The present application is described in further detail below.
制备例1Preparation Example 1
改性木浆纤维的制备方法,包括以下步骤:The method for preparing modified wood pulp fiber comprises the following steps:
称取1kg木浆纤维、0.05kg环氧基硅烷偶联剂、0.05kg乙烯基硅烷偶联剂、0.015kg丙烯腈、0.02kg异戊二烯、0.018kg多胺化合物。其中环氧基硅烷偶联剂选用KH-560,乙烯基硅烷偶联剂选用KH-570,多胺化合物选用丁二胺。Weigh 1kg of wood pulp fiber, 0.05kg of epoxy silane coupling agent, 0.05kg of vinyl silane coupling agent, 0.015kg of acrylonitrile, 0.02kg of isoprene, and 0.018kg of polyamine compound, wherein the epoxy silane coupling agent is KH-560, the vinyl silane coupling agent is KH-570, and the polyamine compound is butanediamine.
另外配置引发剂溶液,引发剂溶液包含2g过氧化苯甲酰和500mL甲苯。In addition, an initiator solution was prepared, which contained 2 g of benzoyl peroxide and 500 mL of toluene.
将木浆纤维分散于7L的80wt%乙醇溶液中,加入环氧基硅烷偶联剂和乙烯基硅烷偶联剂,加热至65℃反应1.5h,反应结束后过滤,得到第一木浆纤维;Dispersing wood pulp fibers in 7 L of 80 wt% ethanol solution, adding epoxy silane coupling agent and vinyl silane coupling agent, heating to 65° C. to react for 1.5 h, filtering after the reaction to obtain first wood pulp fibers;
将第一木浆纤维分散于7L的甲苯中,加入丙烯腈和异戊二烯,加热至95℃,缓慢滴加引发剂溶液,加入完毕后继续反应2h,反应结束后过滤,得到第二木浆纤维;The first wood pulp fiber is dispersed in 7 L of toluene, acrylonitrile and isoprene are added, and the mixture is heated to 95° C. The initiator solution is slowly added dropwise, and the reaction is continued for 2 hours after the addition is completed. After the reaction is completed, the mixture is filtered to obtain the second wood pulp fiber;
将第二木浆纤维分散于5L的50wt%乙醇溶液中,加入50g碳酸钠,搅拌均匀后再加入多胺化合物,加热至55℃反应3h,反应结束后过滤,得到改性木浆纤维。The second wood pulp fiber was dispersed in 5L of 50wt% ethanol solution, 50g of sodium carbonate was added, and the mixture was stirred evenly, and then the polyamine compound was added. The mixture was heated to 55°C and reacted for 3h. After the reaction was completed, the modified wood pulp fiber was filtered to obtain the modified wood pulp fiber.
制备例2Preparation Example 2
改性木浆纤维的制备方法,包括以下步骤:The method for preparing modified wood pulp fiber comprises the following steps:
本制备例与制备例1的区别在于,制备原料用量不同。The difference between this preparation example and preparation example 1 is that the amounts of the preparation raw materials are different.
称取1kg木浆纤维、0.1kg环氧基硅烷偶联剂、0.1kg乙烯基硅烷偶联剂、0.03kg丙烯腈、0.04kg异戊二烯、0.03kg多胺化合物。其中环氧基硅烷偶联剂选用KH-560,乙烯基硅烷偶联剂选用KH-570,多胺化合物选用己二胺。Weigh 1kg of wood pulp fiber, 0.1kg of epoxy silane coupling agent, 0.1kg of vinyl silane coupling agent, 0.03kg of acrylonitrile, 0.04kg of isoprene, and 0.03kg of polyamine compound, wherein the epoxy silane coupling agent is KH-560, the vinyl silane coupling agent is KH-570, and the polyamine compound is hexamethylenediamine.
制备例3Preparation Example 3
改性木浆纤维的制备方法,包括以下步骤:The method for preparing modified wood pulp fiber comprises the following steps:
本制备例与制备例2的区别在于,多胺化合物的用量为0.015kg,多胺化合物选用乙二胺。The difference between this preparation example and preparation example 2 is that the amount of the polyamine compound used is 0.015 kg, and ethylenediamine is selected as the polyamine compound.
制备例4Preparation Example 4
改性木浆纤维的制备方法,包括以下步骤:The method for preparing modified wood pulp fiber comprises the following steps:
称取1kg木浆纤维、0.057kg氨基硅烷偶联剂、0.05kg乙烯基硅烷偶联剂、0.015kg丙烯腈、0.02kg异戊二烯。其中氨基选用KH-550,乙烯基硅烷偶联剂选用KH-570。Weigh 1 kg of wood pulp fiber, 0.057 kg of aminosilane coupling agent, 0.05 kg of vinylsilane coupling agent, 0.015 kg of acrylonitrile, and 0.02 kg of isoprene. The aminosilane coupling agent is KH-550, and the vinylsilane coupling agent is KH-570.
另外配置引发剂溶液,引发剂溶液包含2g过氧化苯甲酰和500mL甲苯。In addition, an initiator solution was prepared, which contained 2 g of benzoyl peroxide and 500 mL of toluene.
将木浆纤维分散于7L的80wt%乙醇溶液中,加入氨基硅烷偶联剂和乙烯基硅烷偶联剂,加热至65℃反应1.5h,反应结束后过滤,得到第一木浆纤维;Dispersing wood pulp fibers in 7 L of 80 wt% ethanol solution, adding aminosilane coupling agent and vinylsilane coupling agent, heating to 65° C. for reaction for 1.5 h, filtering after the reaction to obtain first wood pulp fibers;
将第一木浆纤维分散于7L的甲苯中,加入丙烯腈和异戊二烯,加热至95℃,缓慢滴加引发剂溶液,加入完毕后继续反应2h,反应结束后过滤,得到改性木浆纤维。The first wood pulp fiber was dispersed in 7 L of toluene, acrylonitrile and isoprene were added, and the mixture was heated to 95° C. The initiator solution was slowly added dropwise. After the addition was completed, the reaction was continued for 2 h. After the reaction was completed, the mixture was filtered to obtain modified wood pulp fiber.
制备例5Preparation Example 5
改性木浆纤维的制备方法,包括以下步骤:The method for preparing modified wood pulp fiber comprises the following steps:
称取1kg木浆纤维、0.05kg环氧基硅烷偶联剂、0.018kg多胺化合物。其中环氧基硅烷偶联剂选用KH-560,多胺化合物选用己二胺。Weigh 1 kg of wood pulp fiber, 0.05 kg of epoxy silane coupling agent, and 0.018 kg of polyamine compound, wherein the epoxy silane coupling agent is KH-560, and the polyamine compound is hexamethylenediamine.
将木浆纤维分散于7L的80wt%乙醇溶液中,加入环氧基硅烷偶联剂,加热至65℃反应1.5h,反应结束后过滤,得到第一木浆纤维;Dispersing wood pulp fibers in 7 L of 80 wt% ethanol solution, adding epoxy silane coupling agent, heating to 65° C. for reaction for 1.5 h, filtering after the reaction to obtain first wood pulp fibers;
将第一木浆纤维分散于5L的50wt%乙醇溶液中,加入50g碳酸钠,搅拌均匀后再加入多胺化合物,加热至55℃反应3h,反应结束后过滤,得到改性木浆纤维。The first wood pulp fiber was dispersed in 5L of 50wt% ethanol solution, 50g of sodium carbonate was added, and the mixture was stirred evenly, and then a polyamine compound was added. The mixture was heated to 55°C and reacted for 3h. After the reaction was completed, the mixture was filtered to obtain modified wood pulp fiber.
制备例6Preparation Example 6
改性木浆纤维的制备方法,包括以下步骤:The method for preparing modified wood pulp fiber comprises the following steps:
本制备例与制备例2的区别在于,在制备第二木浆纤维的过程中,不加入丙烯腈,改为加入0.058kg的苯乙烯。The difference between this preparation example and preparation example 2 is that, in the process of preparing the second wood pulp fiber, acrylonitrile is not added, but 0.058 kg of styrene is added instead.
实施例1Example 1
记忆芯体的制备方法,包括以下步骤:The method for preparing a memory core comprises the following steps:
将木浆纤维粉碎和开松,将复合纤维开松,其中木浆纤维选用针叶木纤维,长度2.5mm;复合纤维选用ES纤维,复合纤维的芯层为聚丙烯、表层为聚乙烯,复合纤维纤度为2D,长度8mm。The wood pulp fiber is crushed and opened, and the composite fiber is opened, wherein the wood pulp fiber is coniferous wood fiber with a length of 2.5 mm; the composite fiber is ES fiber, the core layer of the composite fiber is polypropylene, the surface layer is polyethylene, the composite fiber fineness is 2D, and the length is 8 mm.
将木浆纤维和复合纤维混合,进入成型箱内进行打散并呈飘浮状态,在气流作用下到达成网帘,得到粗纤网。The wood pulp fiber and the composite fiber are mixed and put into a forming box to be broken up and floated, and then they reach a net curtain under the action of airflow to obtain a coarse fiber net.
成型箱设置有多个,在前一个成型箱形成粗纤网后,粗纤网进入后一个成型箱,并且相邻成型箱之间设置有树脂下料装置,树脂下料装置用于播撒吸水树脂,吸水树脂为丙烯酸型高分子吸水树脂,选购自春晖高分子材料公司,将吸水树脂播撒至粗纤网,形成纤网,然后在纤网的承载面上继续形成下一个纤网,在本实施例中,成型箱设置有三个。所用木浆纤维、吸水树脂和复合纤维的质量比为10:20:3。There are multiple forming boxes. After the coarse fiber web is formed in the previous forming box, the coarse fiber web enters the next forming box, and a resin feeding device is provided between adjacent forming boxes. The resin feeding device is used to spread water-absorbing resin. The water-absorbing resin is an acrylic polymer water-absorbing resin purchased from Chunhui Polymer Materials Company. The water-absorbing resin is spread on the coarse fiber web to form a fiber web, and then the next fiber web is formed on the supporting surface of the fiber web. In this embodiment, there are three forming boxes. The mass ratio of the wood pulp fiber, water-absorbing resin and composite fiber used is 10:20:3.
成型后纤网进入热风箱,采用热风穿透的方式进行热粘合加固,热风温度为120℃,然后经压实辊压实,冷却,收卷,得到记忆芯体。After forming, the fiber web enters the hot air box and is thermally bonded and reinforced by hot air penetration. The hot air temperature is 120°C. Then it is compacted by a compaction roller, cooled, and rolled up to obtain a memory core.
实施例2Example 2
记忆芯体的制备方法,包括以下步骤:The method for preparing a memory core comprises the following steps:
本实施例与实施例1的区别在于,所用木浆纤维、吸水树脂和复合纤维的质量比为30:100:15。The difference between this embodiment and embodiment 1 is that the mass ratio of the wood pulp fiber, the water-absorbing resin and the composite fiber is 30:100:15.
实施例3Example 3
记忆芯体的制备方法,包括以下步骤:The method for preparing a memory core comprises the following steps:
本实施例与实施例1的区别在于,所用木浆纤维、吸水树脂和复合纤维的质量比为20:50:7。The difference between this embodiment and embodiment 1 is that the mass ratio of the wood pulp fiber, the water-absorbing resin and the composite fiber is 20:50:7.
实施例4~实施例9Embodiment 4 to Embodiment 9
实施例4至实施例9与实施例1的区别在于,木浆纤维选用改性木浆纤维,改性木浆纤维的来源如表1所示。The difference between Example 4 to Example 9 and Example 1 is that the wood pulp fiber is modified wood pulp fiber, and the source of the modified wood pulp fiber is shown in Table 1.
表1Table 1
对比例1Comparative Example 1
记忆芯体的制备方法,包括以下步骤:The method for preparing a memory core comprises the following steps:
本对比例与实施例1的区别在于,不加入复合纤维。The difference between this comparative example and Example 1 is that no composite fiber is added.
对比例2Comparative Example 2
市售的采用无尘纸-高分子树脂-无纺布-高分子树脂-无尘纸结构的复合芯体,无尘纸与高分子树脂之间喷有热熔胶。The composite core body on the market adopts the structure of dust-free paper-polymer resin-non-woven fabric-polymer resin-dust-free paper, and hot melt adhesive is sprayed between the dust-free paper and the polymer resin.
性能测试Performance Testing
参考GB/T 24442.1-2009《纺织品压缩性能的测定》,测试芯体的压缩弹性率,其中以0.02kPa轻压10s,以1kPa重压60s,恢复时间60s,测试结果如表2所示。With reference to GB/T 24442.1-2009 “Determination of compression properties of textiles”, the compression elasticity of the core was tested, with a light pressure of 0.02 kPa for 10 s, a heavy pressure of 1 kPa for 60 s, and a recovery time of 60 s. The test results are shown in Table 2.
取100mL生理盐水(质量浓度0.9%)并加热至40℃,然后将生理盐水加入芯体,吸收芯体试样置于40±1℃、65±1%RH试验箱中10min,然后取出吸收芯体试样进行测试;测试人员两手分别握住吸收芯体试样的两端,首先是一手甩动吸收芯体试样的一端,重复10次,然后两手往复拉伸吸收芯体试样的两端,重复10次,然后两手揉搓芯体,重复10次,最后观察吸收芯体是否出现起坨的现象,并将现象结果记录于表2。Take 100mL of normal saline (mass concentration 0.9%) and heat it to 40°C, then add the normal saline to the core, place the absorbent core sample in a 40±1°C, 65±1%RH test box for 10 minutes, and then take out the absorbent core sample for testing; the tester holds the two ends of the absorbent core sample with both hands, first swings one end of the absorbent core sample with one hand, repeats 10 times, then stretches the two ends of the absorbent core sample back and forth with both hands, repeats 10 times, then rubs the core with both hands, repeats 10 times, and finally observes whether the absorbent core has any lumping phenomenon, and records the phenomenon results in Table 2.
参考QB/T 5650-2021《一次性纸制卫生用品用复合吸收芯体》,测试芯体的吸收倍率、吸收速度和回渗量,测试溶液分别选用生理盐水、模拟经血和牛奶,测试结果记录于表3。Referring to QB/T 5650-2021 "Composite absorbent core for disposable paper sanitary products", the absorption rate, absorption rate and rewet amount of the core were tested. The test solutions were normal saline, simulated menstrual blood and milk, and the test results are recorded in Table 3.
表2Table 2
表3Table 3
从表2可以看出,与传统的无纺布-吸水树脂的复合芯体以及木浆纤维-吸水树脂的木浆芯体相比,由木浆纤维-吸水树脂-复合纤维组成的记忆芯体兼具不起坨、压缩弹性率高的优点,即结构稳定且弹性和舒适度高。As can be seen from Table 2, compared with the traditional non-woven fabric-water-absorbent resin composite core and the wood pulp core of wood pulp fiber-water-absorbent resin, the memory core composed of wood pulp fiber-water-absorbent resin-composite fiber has the advantages of no lumping and high compression elasticity, that is, the structure is stable and has high elasticity and comfort.
结合表3分析,对于芯体基础的吸液和储液能力,由木浆纤维-吸水树脂-复合纤维组成的记忆芯体,对于生理盐水、模拟经血和牛奶均具有较高的吸收倍率、较快的吸收速度和较小的回渗量,因此记忆芯体面对各种使用场景均表现出良好的吸液和储液能力,可应用于纸尿裤、卫生巾、哺乳吸奶巾、吸汗巾和厨房纸等领域。Combined with the analysis in Table 3, for the liquid absorption and storage capacity of the core base, the memory core composed of wood pulp fiber-absorbent resin-composite fiber has a higher absorption rate, faster absorption speed and smaller re-seepage amount for physiological saline, simulated menstrual blood and milk. Therefore, the memory core shows good liquid absorption and storage capacity in various usage scenarios and can be applied to diapers, sanitary napkins, breastfeeding wipes, sweat-absorbing wipes and kitchen paper.
结合实施例1与实施例4-5相比较,可以看出采用改性后的木浆纤维能够发挥更好的吸液储液效果,并且以较难吸收的模拟经血和牛奶作为测试溶液时,同样获得明显的吸液储液效果。By comparing Example 1 with Examples 4-5, it can be seen that the modified wood pulp fiber can achieve better liquid absorption and storage effects, and when the difficult-to-absorb simulated menstrual blood and milk are used as test solutions, obvious liquid absorption and storage effects are also obtained.
结合实施例5与实施例6相比较,可以看出与乙二胺作为多胺化合物来改性木浆纤维相比,己二胺这类长链的多胺化合物具有更好的改性效果;结合实施例5与实施例7相比较,可以看出与直接通过氨基硅烷偶联剂接入木浆纤维相比,先用环氧基硅烷偶联剂接入木浆纤维,再用己二胺与环氧基反应连接来实现接入,对木浆纤维的改性效果以及最终芯体的吸液储液效果有更好的提升。By comparing Example 5 with Example 6, it can be seen that compared with using ethylenediamine as a polyamine compound to modify wood pulp fibers, long-chain polyamine compounds such as hexamethylenediamine have better modification effects; by comparing Example 5 with Example 7, it can be seen that compared with directly accessing wood pulp fibers through aminosilane coupling agents, first accessing wood pulp fibers with epoxy silane coupling agents and then using hexamethylenediamine to react with epoxy groups to achieve access, the modification effect of wood pulp fibers and the final liquid absorption and storage effects of the core are better improved.
结合实施例5与实施例8-9相比较,可以看出木浆纤维改性接入丙烯腈-异戊二烯共聚物,有助于提高木浆纤维与复合纤维的相容性,从而促使组成芯体的纤网稳定性更高,芯体内的导流通道更稳定,进而提高芯体的吸液能力和储液能力。By comparing Example 5 with Examples 8-9, it can be seen that the modification of wood pulp fibers by accession of acrylonitrile-isoprene copolymer helps to improve the compatibility of wood pulp fibers with composite fibers, thereby making the fiber web constituting the core more stable and the flow guide channels in the core more stable, thereby improving the liquid absorption and storage capabilities of the core.
本具体实施方式仅仅是对本申请的解释,其并不是对本申请的限制,本领域技术人员在阅读完本说明书后可以根据需要对本具体实施方式做出没有创造性贡献的修改,但只要在本申请的权利要求范围内都受到专利法的保护。This specific implementation manner is merely an explanation of the present application and is not a limitation of the present application. After reading this specification, those skilled in the art may make non-creative modifications to the specific implementation manner as needed, but such modifications are protected by the patent law as long as they are within the scope of the claims of the present application.
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