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CN111662672A - Hydrophilic adhesive and synthesis method and application thereof - Google Patents

Hydrophilic adhesive and synthesis method and application thereof Download PDF

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Publication number
CN111662672A
CN111662672A CN201910167487.5A CN201910167487A CN111662672A CN 111662672 A CN111662672 A CN 111662672A CN 201910167487 A CN201910167487 A CN 201910167487A CN 111662672 A CN111662672 A CN 111662672A
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core body
hydrophilic adhesive
adhesive
hydrophilic
polyhydroxy
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霍毅松
庄孝根
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GAUNGZHOU DEYUAN FINE CHEMICAL CO Ltd
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GAUNGZHOU DEYUAN FINE CHEMICAL CO Ltd
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04Polyurethanes
    • C09J175/08Polyurethanes from polyethers
    • 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
    • A61L15/42Use of materials characterised by their function or physical properties
    • A61L15/58Adhesives
    • A61L15/585Mixtures of macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/4009Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4018Mixtures of compounds of group C08G18/42 with compounds of group C08G18/48
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4202Two or more polyesters of different physical or chemical nature
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4804Two or more polyethers of different physical or chemical nature

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Materials Engineering (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Absorbent Articles And Supports Therefor (AREA)

Abstract

The invention discloses a hydrophilic adhesive and a synthesis method and application thereof. The synthesis method comprises the following steps: the hydrophilic adhesive is formed by copolymerization reaction of a uniform mixed reaction system containing polyhydroxy polyether, polyhydroxy polyester and polyfunctional group isocyanate. The synthetic method of the hydrophilic adhesive is simple in process, and the obtained hydrophilic adhesive is coated on the wrapping layer of the non-woven fabric core body and then is attached to the core body. Because the adhesive is polar and hydrophilic, the wrapping layer of the non-woven fabric core body can still maintain certain hydrophilicity relative to a rubber adhesive after the core body absorbs urine and the hydrophilic agent of the wrapping layer of the non-woven fabric core body is eluted, so that the wrapping layer has better attaching and adhering properties to the core body material after water absorption, the core body after water absorption maintains certain physical wrapping property, the complete state of the core body can be maintained greatly, and the application prospect is wide.

Description

一种亲水性胶粘剂及其合成方法与应用A kind of hydrophilic adhesive and its synthesis method and application

技术领域technical field

本发明涉及一种亲水性胶粘剂,尤其涉及一种应用于无纺布包裹木浆与吸水高分子混合而成的纸尿裤芯体的亲水性胶粘剂及其合成方法,以及其应用。The invention relates to a hydrophilic adhesive, in particular to a hydrophilic adhesive applied to the core of a diaper which is formed by wrapping wood pulp and a water-absorbing polymer in a non-woven fabric, and a method for synthesizing the same, and applications thereof.

背景技术Background technique

婴儿或成人纸尿裤的结构的关键组成部分为能够吸收尿液的芯体。纸尿裤生产厂家在生产的过程中通过有效混合吸水树脂与木浆纤维,以吸水树脂与木浆纤维的混合物作为芯体。传统芯体为高分子吸水树脂与木浆纤维的混合物,并成型后使用无尘纸、无纺布等包裹后集成到纸尿裤结构中。使用无纺布包裹的芯体,较无尘纸包裹的芯体,有更柔软,更轻薄的优势。无纺布使用橡胶基热熔胶粘合在芯体上,起到包裹作用。但是无纺布包裹的芯体弱点在于,吸收尿液后,由于无纺布纤维表面的亲水处理剂被洗脱,无纺布和橡胶基热熔胶都体现出非极性不亲水的性能,从而,难于与吸收了液体的芯体木浆和高分子吸水树脂保持紧密的贴合。从而,包裹层不再对芯体的材料有物理包裹作用。而芯体的木浆和吸水树脂在吸水后呈分散的颗粒状,在物理包裹作用失效的情况下,非常容易散开,产生堆垛现象,表现为纸尿裤芯体的断层。对使用者来说,是一个很差的使用体验。A key component of the construction of a baby or adult diaper is the core that absorbs urine. In the production process, diaper manufacturers effectively mix water-absorbent resin and wood pulp fiber, and use the mixture of water-absorbent resin and wood pulp fiber as the core. The traditional core is a mixture of polymer water-absorbing resin and wood pulp fiber, which is wrapped with clean paper and non-woven fabric after molding and integrated into the diaper structure. The core body wrapped with non-woven fabric is softer and thinner than the core body wrapped with dust-free paper. The non-woven fabric is bonded to the core with a rubber-based hot melt adhesive, which plays a wrapping role. However, the weakness of the core wrapped by the non-woven fabric is that after absorbing urine, the non-woven fabric and rubber-based hot melt adhesive both show non-polar and non-hydrophilic properties due to the elution of the hydrophilic treatment agent on the surface of the non-woven fabric fiber. Therefore, it is difficult to maintain a tight fit with the liquid-absorbing core wood pulp and the high-molecular water-absorbent resin. Thus, the wrapping layer no longer has a physical wrapping effect on the material of the core. The wood pulp and water-absorbent resin in the core are in the form of dispersed particles after absorbing water. When the physical wrapping function fails, it is very easy to spread out, resulting in a stacking phenomenon, which is manifested as a fault in the core of the diaper. For users, it is a very poor experience.

发明内容SUMMARY OF THE INVENTION

本发明的主要目的在于提供一种亲水性胶粘剂及其合成方法与应用,以克服现有技术的不足。The main purpose of the present invention is to provide a hydrophilic adhesive and its synthesis method and application to overcome the deficiencies of the prior art.

为实现前述发明目的,本发明采用的技术方案包括:In order to realize the foregoing invention purpose, the technical scheme adopted in the present invention includes:

本发明实施例提供了一种亲水性胶粘剂的合成方法,其包括:使包含多羟基聚醚、多羟基聚酯和多官能团异氰酸酯的均匀混合反应体系共聚反应形成亲水性胶粘剂。An embodiment of the present invention provides a method for synthesizing a hydrophilic adhesive, which includes: copolymerizing a uniformly mixed reaction system comprising polyhydroxy polyether, polyhydroxy polyester and multifunctional isocyanate to form a hydrophilic adhesive.

在一些实施例中,所述多羟基聚醚包括两官能团聚乙二醇、两官能团聚丙二醇、三官能团聚丙二醇中的任意一种或两种以上的组合。In some embodiments, the polyhydroxy polyether includes any one or a combination of two or more of difunctional polyethylene glycol, difunctional polypropylene glycol, and trifunctional polypropylene glycol.

在一些实施例中,所述多羟基聚酯包括两官能团聚己二酸乙二醇、两官能团聚己二酸丙二醇、两官能团聚己二酸新戊二醇、两官能团聚邻苯二甲酸乙二醇、两官能团聚邻苯二甲酸丙二醇、两官能团聚邻苯二甲酸新戊二醇中的任意一种或两种以上的组合。In some embodiments, the polyhydroxy polyester includes difunctional polyethylene adipate, difunctional polypropylene adipate, difunctional polyneopentyl adipate, difunctional polyethylene phthalate Any one or a combination of two or more of diols, difunctional polypropylene phthalate, and difunctional polyneopentyl phthalate.

进一步地,所述多官能团异氰酸酯包括MDI。Further, the multifunctional isocyanate includes MDI.

本发明实施例还提供了由前述方法合成的亲水性胶粘剂,其包括由多羟基聚醚、多羟基聚酯和多官能团异氰酸酯共聚反应形成的共聚物。The embodiment of the present invention also provides a hydrophilic adhesive synthesized by the aforementioned method, which comprises a copolymer formed by the copolymerization reaction of polyhydroxy polyether, polyhydroxy polyester and polyfunctional isocyanate.

本发明实施例还提供了前述的亲水性胶粘剂于婴儿或成人纸尿裤制作领域中的应用。The embodiments of the present invention also provide the application of the aforementioned hydrophilic adhesive in the field of making baby or adult diapers.

进一步地,所述应用包括:将所述亲水性胶粘剂施加于无纺布芯体包裹层上,使所述无纺布芯体包裹层与芯体贴合。Further, the application includes: applying the hydrophilic adhesive on the non-woven core wrapping layer, so that the non-woven fabric core wrapping layer is attached to the core body.

现有技术相比,本发明的优点包括:Compared with the prior art, the advantages of the present invention include:

本发明提供的亲水性胶粘剂的合成方法工艺简单,将所获亲水性胶粘剂涂布于无纺布芯体包裹层后,与芯体贴合。由于本发明胶粘剂呈极性和亲水性,从而在芯体吸收尿液、无纺布芯体包裹层亲水剂被洗脱后,相对于橡胶系胶粘剂,仍能保持包裹层一定的亲水性,从而使包裹层对吸水后的芯体材料有更好的贴合附着性能,从而使吸水后的芯体保持一定的物理包裹性能,更大可能保持芯体的完整状态。The synthetic method of the hydrophilic adhesive provided by the invention is simple in process, and the obtained hydrophilic adhesive is coated on the non-woven core body wrapping layer and then attached to the core body. Since the adhesive of the present invention is polar and hydrophilic, after the core absorbs urine and the hydrophilic agent of the non-woven core wrapping layer is eluted, relative to the rubber-based adhesive, the wrapping layer can still maintain a certain hydrophilicity Therefore, the wrapping layer has better adhesion and adhesion performance to the core material after water absorption, so that the core body after water absorption maintains a certain physical wrapping performance, and it is more likely to maintain the integrity of the core body.

具体实施方式Detailed ways

如前所述,鉴于现有技术的缺陷,本案发明人经长期研究和大量实践,得以提出本发明的技术方案,其主要是提供一种亲水性的胶粘剂,涂布于无纺布包裹层后,与芯体贴合。由于胶粘剂呈极性和亲水性,从而在芯体吸收尿液,无纺布包裹层亲水剂被洗脱后,相对于橡胶系胶粘剂,仍能保持包裹层一定的亲水性,从而,使包裹层对芯体有一定的贴附力,使芯体有更大可能保持完整状态。如下将对该技术方案、其实施过程及原理等作进一步的解释说明。As mentioned above, in view of the defects of the prior art, the inventor of the present case has been able to propose the technical solution of the present invention after long-term research and extensive practice, which mainly provides a hydrophilic adhesive, which is coated on the non-woven wrapping layer Then, fit with the core body. Since the adhesive is polar and hydrophilic, after the core absorbs urine and the hydrophilic agent of the non-woven wrapping layer is eluted, the wrapping layer can still maintain a certain degree of hydrophilicity compared with the rubber-based adhesive, thus, The wrapping layer has a certain adhesion to the core body, so that the core body has a greater possibility to remain intact. The technical solution, its implementation process and principle will be further explained as follows.

作为本发明技术方案的一个方面,其所涉及的系一种亲水性胶粘剂的合成方法,其包括:使包含多羟基聚醚、多羟基聚酯和多官能团异氰酸酯的均匀混合反应体系共聚反应形成极性的亲水性胶粘剂。As one aspect of the technical solution of the present invention, it relates to a method for synthesizing a hydrophilic adhesive, which comprises: copolymerizing a uniformly mixed reaction system comprising polyhydroxy polyether, polyhydroxy polyester and polyfunctional isocyanate to form Polar hydrophilic adhesive.

在一些实施例中,所述多羟基聚醚包括两官能团聚乙二醇、两官能团聚丙二醇、三官能团聚丙二醇等预聚体中的任意一种或两种以上的组合,但不限于此。In some embodiments, the polyhydroxy polyether includes any one or a combination of two or more prepolymers such as difunctional polyethylene glycol, difunctional polypropylene glycol, and trifunctional polypropylene glycol, but is not limited thereto.

进一步地,所述多羟基聚醚的质均分子量为1000~5000。Further, the mass average molecular weight of the polyhydroxy polyether is 1000-5000.

在一些实施例中,所述多羟基聚酯包括两官能团聚己二酸乙二醇、两官能团聚己二酸丙二醇、两官能团聚己二酸新戊二醇、两官能团聚邻苯二甲酸乙二醇、两官能团聚邻苯二甲酸丙二醇、两官能团聚邻苯二甲酸新戊二醇体系等中的任意一种或两种以上的组合,但不限于此。In some embodiments, the polyhydroxy polyester includes difunctional polyethylene adipate, difunctional polypropylene adipate, difunctional polyneopentyl adipate, difunctional polyethylene phthalate Any one or a combination of two or more of diols, bifunctional polypropylene phthalate, and bifunctional polyneopentyl phthalate systems, etc., but not limited thereto.

进一步地,所述多羟基聚酯的质均分子量为1000~3000。Further, the mass average molecular weight of the polyhydroxy polyester is 1000-3000.

在一些实施例中,所述多官能团异氰酸酯选用MDI,但不限于此。In some embodiments, MDI is selected as the multifunctional isocyanate, but not limited thereto.

在一些实施例中,所述均匀混合反应体系包括按照质量百分比计算的如下组分:25~65wt%多羟基聚醚、29~60wt%多羟基聚酯和6~15wt%MDI。In some embodiments, the uniformly mixed reaction system includes the following components calculated by mass percentage: 25-65 wt % polyhydroxy polyether, 29-60 wt % polyhydroxy polyester and 6-15 wt % MDI.

在一些实施例中,所述共聚反应的温度为60~160℃,时间为0.5~4h。In some embodiments, the temperature of the copolymerization reaction is 60-160° C., and the time is 0.5-4 h.

作为本发明技术方案的另一个方面,其所涉及的系由前述方法合成的亲水性胶粘剂,其包括由多羟基聚醚、多羟基聚酯和多官能团异氰酸酯共聚反应形成的共聚物。As another aspect of the technical solution of the present invention, the related hydrophilic adhesive is synthesized by the aforementioned method, which includes a copolymer formed by the copolymerization reaction of polyhydroxy polyether, polyhydroxy polyester and polyfunctional isocyanate.

进一步地,所述亲水性胶粘剂在温度为160℃的条件下的粘度为500~20000cps。Further, the viscosity of the hydrophilic adhesive at a temperature of 160° C. is 500-20,000 cps.

本发明实施例的另一个方面还提供了前述的亲水性胶粘剂于婴儿或成人纸尿裤制作领域中的应用。Another aspect of the embodiments of the present invention also provides the application of the aforementioned hydrophilic adhesive in the field of making baby or adult diapers.

进一步地,所述应用包括:将所述亲水性胶粘剂施加于无纺布芯体包裹层上,使所述无纺布芯体包裹层与芯体贴合。Further, the application includes: applying the hydrophilic adhesive on the non-woven core wrapping layer, so that the non-woven fabric core wrapping layer is attached to the core body.

更进一步地,所述应用包括:至少采用刮胶、点胶、喷胶等施加方法中的任一种方式将所述亲水性胶粘剂施胶于无纺布芯体包裹层上。Further, the application includes: applying the hydrophilic adhesive to the non-woven core wrapping layer by at least any one of application methods such as squeegee, glue dispensing, and glue spraying.

藉由上述技术方案,本发明提供的亲水性胶粘剂的合成方法工艺简单,将所获亲水性胶粘剂涂布于无纺布芯体包裹层后,与芯体贴合。由于本发明胶粘剂呈极性和亲水性,从而在芯体吸收尿液、无纺布芯体包裹层亲水剂被洗脱后,相对于橡胶系胶粘剂,仍能保持包裹层一定的亲水性,从而使包裹层对吸水后的芯体材料有更好的贴合附着性能,从而使吸水后的芯体保持一定的物理包裹性能,更大可能保持芯体的完整状态。With the above technical solutions, the synthetic method of the hydrophilic adhesive provided by the present invention is simple in process. Since the adhesive of the present invention is polar and hydrophilic, after the core absorbs urine and the hydrophilic agent of the non-woven core wrapping layer is eluted, relative to the rubber-based adhesive, the wrapping layer can still maintain a certain hydrophilicity Therefore, the wrapping layer has better adhesion and adhesion performance to the core material after water absorption, so that the core body after water absorption maintains a certain physical wrapping performance, and it is more likely to maintain the integrity of the core body.

以下通过若干实施例进一步详细说明本发明的技术方案。显然,所描述的实施例仅仅是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动的前提下所获得的所有其他实施例,都属于本发明保护的范围。The technical solutions of the present invention are further described in detail below through several embodiments. Obviously, the described embodiments are only some, but not all, embodiments of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative work fall within the protection scope of the present invention.

实施例1Example 1

将分子量为3000的二官能团聚己二酸乙二醇聚酯100g、分子量为3000的二官能团聚乙二醇聚醚180g、分子量为5000的3官能团聚丙二醇聚醚30g、分子量为1600的聚邻苯二甲酸乙二醇聚酯30g、MDI 35g混合均匀,并在120℃下反应1小时。100 g of difunctional polyethylene adipate polyester with molecular weight of 3000, 180 g of difunctional polyethylene glycol polyether with molecular weight of 3000, 30 g of trifunctional polypropylene glycol polyether with molecular weight of 5000, and polyoxyethylene with molecular weight of 1600 30 g of ethylene phthalate polyester and 35 g of MDI were mixed uniformly and reacted at 120° C. for 1 hour.

经测试,本实施例所获合成产物亲水性胶粘剂在160℃下的粘度为5600。After testing, the viscosity of the synthetic product hydrophilic adhesive obtained in this example at 160° C. is 5600.

在140℃下,将本实施例所获合成产物亲水性胶粘剂涂布施胶在无纺布表面,贴合于木浆与吸水高分子混合而成的芯体材料表面,形成有效贴合。At 140°C, the hydrophilic adhesive of the synthetic product obtained in this example was coated and sizing on the surface of the non-woven fabric, and was attached to the surface of the core material mixed with wood pulp and water-absorbing polymer to form an effective attachment.

测试例test case

同样使用市售橡胶基热熔胶涂布于无纺布表面样品做对比,贴合面积为5厘米*5厘米,使用150毫升生理盐水,倒于贴合部位。待生理盐水全部被吸收后,揭下贴合无纺布。Also use commercially available rubber-based hot-melt adhesive to coat the non-woven surface samples for comparison. The bonding area is 5 cm * 5 cm. Use 150 ml of normal saline and pour it on the bonding site. After all the normal saline is absorbed, remove the non-woven fabric.

橡胶基涂布的表面,其沾有的木浆和吸水高分子在摩擦后均易脱落,而本实施例的亲水胶粘剂摩擦后难于脱落。On the rubber-based coated surface, the wood pulp and water-absorbing polymer on the surface are easy to fall off after rubbing, while the hydrophilic adhesive of this embodiment is difficult to fall off after rubbing.

在将亲水性胶粘剂贴合的木浆和吸水高分子全部去除后,两片样品再次贴合于以上吸过水的芯体表面,再次揭开后,橡胶基胶粘剂的样品表面,完全不贴合木浆和吸水高分子。而本实施例的亲水性胶粘剂表面再次贴附满了木浆及吸水高分子。After all the wood pulp and water-absorbing polymer bonded by the hydrophilic adhesive were removed, the two samples were again bonded to the surface of the core that had absorbed water. Combining wood pulp and water-absorbing polymers. On the other hand, the surface of the hydrophilic adhesive of this embodiment is covered with wood pulp and water-absorbing polymers again.

因此可以看出,本实施例的亲水性胶粘剂对吸水后的芯体材料有更好的贴合附着性能,从而对吸水后的芯体保持一定的物理包裹性能,维持芯体的完整性。Therefore, it can be seen that the hydrophilic adhesive of this embodiment has better adhesion and adhesion performance to the core material after water absorption, thereby maintaining a certain physical wrapping performance for the core body after water absorption, and maintaining the integrity of the core body.

实施例2Example 2

将分子量为3000的二官能团聚己二酸乙二醇聚酯100g、分子量为3000的二官能团聚乙二醇聚醚40g、分子量为5000的3官能团聚丙二醇聚醚20g、分子量为4000的二官能团聚丙二醇聚醚20g、MDI 15g混合均匀,并在90℃下反应2小时。100 g of bifunctional polyethylene adipate polyester with molecular weight of 3000, 40 g of bifunctional polyethylene glycol polyether with molecular weight of 3000, 20 g of trifunctional polypropylene glycol polyether with molecular weight of 5000, and bifunctional with molecular weight of 4000 20 g of agglomerated propylene glycol polyether and 15 g of MDI were mixed uniformly and reacted at 90° C. for 2 hours.

在140℃下,将本实施例所获合成产物亲水性胶粘剂使用0.6毫米针头点胶在无纺布表面,贴合于木浆与吸水高分子混合而成的芯体材料表面,形成有效贴合。At 140°C, the hydrophilic adhesive of the synthetic product obtained in this example was dispensed on the surface of the non-woven fabric using a 0.6 mm needle, and then adhered to the surface of the core material mixed with wood pulp and water-absorbing polymer to form an effective sticker. combine.

实施例3Example 3

将分子量为2000的二官能团聚己二酸乙二醇聚酯100g、分子量为1000的二官能团聚丙二醇聚醚50g、分子量为5000的3官能团聚丙二醇聚醚150g、MDI 40g混合均匀,并在110℃下反应0.5小时,之后升温到140℃反应1小时。所形成的粘合剂在160℃下可涂布于基板上。使用纯净水滴加在胶层表面,水滴可铺展润湿胶层表面。而涂布的橡胶基胶粘剂,水滴在其表面不铺展,不润湿。Mix 100 g of difunctional polyethylene adipate polyester with a molecular weight of 2000, 50 g of difunctional polypropylene glycol polyether with a molecular weight of 1000, 150 g of trifunctional polypropylene glycol polyether with a molecular weight of 5000, and 40 g of MDI. The reaction was carried out at °C for 0.5 hour, and then the temperature was raised to 140 °C for 1 hour. The resulting adhesive can be coated on a substrate at 160°C. Use pure water droplets on the surface of the adhesive layer, the water droplets can spread and wet the surface of the adhesive layer. For the coated rubber-based adhesive, the water droplets do not spread on the surface and do not wet.

实施例4Example 4

将分子量为1000的二官能团聚己二酸乙二醇聚酯142g、分子量为4000的二官能团聚丙二醇聚醚40g、分子量为5000的3官能团聚丙二醇聚醚20g、MDI 22g混合均匀,并在100℃下反应2小时。所形成的粘合剂在120℃下可涂布于基板上。使用纯净水滴加在胶层表面,水滴可铺展润湿胶层表面。而涂布的橡胶基胶粘剂,水滴在其表面不铺展,不润湿。Mix 142 g of difunctional polyethylene adipate polyester with a molecular weight of 1000, 40 g of difunctional polypropylene glycol polyether with a molecular weight of 4000, 20 g of trifunctional polypropylene glycol polyether with a molecular weight of 5000, and 22 g of MDI. The reaction was carried out at °C for 2 hours. The formed adhesive can be coated on the substrate at 120°C. Use pure water droplets on the surface of the adhesive layer, the water droplets can spread and wet the surface of the adhesive layer. For the coated rubber-based adhesive, the water droplets do not spread on the surface and do not wet.

实施例5Example 5

将分子量为3000的二官能团聚己二酸乙二醇聚酯85g、分子量为4000的二官能团聚丙二醇聚醚130g、分子量为5000的3官能团聚丙二醇聚醚60g、MDI 18g混合均匀,并在60℃下反应1小时,后逐步升温至140℃保持3h,所形成的粘合剂在140℃下可涂布于基板上。使用纯净水滴加在胶层表面,水滴可铺展润湿胶层表面。而涂布的橡胶基胶粘剂,水滴在其表面不铺展,不润湿。Mix 85 g of difunctional polyethylene adipate polyester with a molecular weight of 3000, 130 g of difunctional polypropylene glycol polyether with a molecular weight of 4000, 60 g of trifunctional polypropylene glycol polyether with a molecular weight of 5000, and 18 g of MDI. After the reaction was carried out at 140°C for 1 hour, the temperature was gradually raised to 140°C for 3 hours, and the formed adhesive could be coated on the substrate at 140°C. Use pure water droplets on the surface of the adhesive layer, the water droplets can spread and wet the surface of the adhesive layer. For the coated rubber-based adhesive, the water droplets do not spread on the surface and do not wet.

实施例6Example 6

将分子量为3000的二官能团聚己二酸乙二醇聚酯100g、分子量为3000的二官能团聚乙二醇聚醚40g、分子量为5000的3官能团聚丙二醇聚醚20g、分子量为4000的二官能团聚丙二醇聚醚20g、MDI 15g混合均匀,并在160℃下反应0.5小时。100 g of bifunctional polyethylene adipate polyester with molecular weight of 3000, 40 g of bifunctional polyethylene glycol polyether with molecular weight of 3000, 20 g of trifunctional polypropylene glycol polyether with molecular weight of 5000, and bifunctional with molecular weight of 4000 20 g of agglomerated propylene glycol polyether and 15 g of MDI were mixed uniformly and reacted at 160° C. for 0.5 hour.

在140℃下,将本实施例所获合成产物亲水性胶粘剂使用0.6毫米针头点胶在无纺布表面,贴合于木浆与吸水高分子混合而成的芯体材料表面,形成有效贴合。At 140°C, the hydrophilic adhesive of the synthetic product obtained in this example was dispensed on the surface of the non-woven fabric using a 0.6 mm needle, and then adhered to the surface of the core material mixed with wood pulp and water-absorbing polymer to form an effective sticker. combine.

综上所述,藉由本发明的上述技术方案,本发明的亲水性的胶粘剂,涂布于无纺布包裹层后,与芯体贴合。由于胶粘剂呈极性和亲水性,从而在芯体吸收尿液,无纺布包裹层亲水剂被洗脱后,相对于橡胶系胶粘剂,仍能保持包裹层一定的亲水性,从而使包裹层对芯体有一定的贴附力,使芯体有更大可能保持完整状态,应用前景广泛。To sum up, with the above technical solutions of the present invention, the hydrophilic adhesive of the present invention is applied to the non-woven fabric wrapping layer and then attached to the core. Since the adhesive is polar and hydrophilic, after the core absorbs urine and the hydrophilic agent of the non-woven wrapping layer is eluted, relative to the rubber-based adhesive, the wrapping layer can still maintain a certain degree of hydrophilicity, so that the The wrapping layer has a certain adhesion force to the core, which makes the core more likely to remain intact, and has wide application prospects.

此外,本案发明人还参照实施例1~6的方式,以本说明书中列出的其它原料和条件等进行了试验,并同样制得了呈极性和亲水性,使包裹层对芯体有一定的贴附力,使芯体有更大可能保持完整状态的亲水性胶粘剂。In addition, the inventors of the present application also carried out tests with other raw materials and conditions listed in this specification with reference to the methods of Examples 1 to 6, and also obtained polar and hydrophilic products, so that the wrapping layer has a positive effect on the core body. A hydrophilic adhesive with a certain adhesive force that makes the core more likely to remain intact.

应当理解,上述实施例仅为说明本发明的技术构思及特点,其目的在于让熟悉此项技术的人士能够了解本发明的内容并据以实施,并不能以此限制本发明的保护范围。凡根据本发明精神实质所作的等效变化或修饰,都应涵盖在本发明的保护范围之内。It should be understood that the above-mentioned embodiments are only intended to illustrate the technical concept and characteristics of the present invention, and the purpose thereof is to enable those who are familiar with the art to understand the content of the present invention and implement it accordingly, and cannot limit the protection scope of the present invention. All equivalent changes or modifications made according to the spirit of the present invention should be included within the protection scope of the present invention.

Claims (10)

1. A method for synthesizing a hydrophilic adhesive is characterized by comprising the following steps: the hydrophilic adhesive is formed by copolymerization reaction of a uniform mixed reaction system containing polyhydroxy polyether, polyhydroxy polyester and polyfunctional group isocyanate.
2. The method of synthesis according to claim 1, characterized in that: the polyhydroxy polyether comprises any one or the combination of more than two of difunctional polyethylene glycol, difunctional polypropylene glycol and trifunctional polypropylene glycol; and/or the mass average molecular weight of the polyhydroxy polyether is 1000-5000.
3. The method of synthesis according to claim 1, characterized in that: the polyhydroxy polyester comprises any one or the combination of more than two of difunctional poly (ethylene adipate) glycol, difunctional poly (propylene adipate) glycol, difunctional poly (neopentyl adipate) glycol, difunctional poly (ethylene phthalate) glycol, difunctional poly (propylene phthalate) glycol and difunctional poly (neopentyl phthalate); and/or the mass average molecular weight of the polyhydroxy polyester is 1000-3000.
4. The method of synthesis according to claim 1, characterized in that: the polyfunctional isocyanate comprises MDI.
5. The synthesis method of claim 1, wherein the homogeneous mixing reaction system comprises the following components in percentage by mass: 25-65 wt% of polyhydroxy polyether, 29-60 wt% of polyhydroxy polyester and 6-15 wt% of MDI.
6. The method of synthesis according to claim 1, characterized in that: the temperature of the copolymerization reaction is 60-160 ℃, and the time is 0.5-4 h.
7. A hydrophilic adhesive synthesized by the method of any one of claims 1-6 comprising a copolymer formed by copolymerization of a polyhydroxy polyether, a polyhydroxy polyester, and a polyfunctional isocyanate.
8. The hydrophilic adhesive of claim 7, wherein: the viscosity of the hydrophilic adhesive is 500-20000 cps at 160 ℃.
9. Use of the hydrophilic adhesive of claim 7 or 8 in the field of baby or adult diaper manufacture.
10. The application according to claim 9, wherein the application comprises: applying the hydrophilic adhesive to the non-woven fabric core body wrapping layer to enable the non-woven fabric core body wrapping layer to be attached to the core body; preferably, the application comprises: and applying the hydrophilic adhesive on the non-woven fabric core wrapping layer by adopting any one of glue scraping, glue dispensing and glue spraying.
CN201910167487.5A 2019-03-06 2019-03-06 Hydrophilic adhesive and synthesis method and application thereof Pending CN111662672A (en)

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