CN107760245A - The compound PUR Reactive hot melt adhesives and preparation method thereof of fabric - Google Patents

The compound PUR Reactive hot melt adhesives and preparation method thereof of fabric Download PDF

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Publication number
CN107760245A
CN107760245A CN201610684921.3A CN201610684921A CN107760245A CN 107760245 A CN107760245 A CN 107760245A CN 201610684921 A CN201610684921 A CN 201610684921A CN 107760245 A CN107760245 A CN 107760245A
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CN
China
Prior art keywords
parts
hot melt
reactive hot
compound
melt adhesives
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Pending
Application number
CN201610684921.3A
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Chinese (zh)
Inventor
王以元
咸曦晨
李洪霞
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Land Chemical (kunshan) Co Ltd
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Land Chemical (kunshan) Co Ltd
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Priority to CN201610684921.3A priority Critical patent/CN107760245A/en
Publication of CN107760245A publication Critical patent/CN107760245A/en
Pending legal-status Critical Current

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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
    • C09J175/06Polyurethanes from polyesters
    • 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
    • C08G18/2805Compounds having only one group containing active hydrogen
    • C08G18/288Compounds containing at least one heteroatom other than oxygen or nitrogen
    • C08G18/289Compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
    • 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
    • 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
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/04Non-macromolecular additives inorganic
    • 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
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/08Macromolecular additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

The invention provides a kind of compound PUR Reactive hot melt adhesives and preparation method thereof of fabric.Reactive hot melt adhesive by weight, is made up of following raw material:50 70 parts of toluene di-isocyanate(TDI), 20 25 parts of crystalline polymer polyalcohol, 12 parts of end-capping reagent, 5 15 parts of tackifying resin, 5 10 parts of filler, 15 parts of carbon black, 15 parts of silica gel, 15 parts of calcium hydroxide, 02 parts of coupling agent, 02 parts of plasticizer, 02 parts of ultraviolet absorber, 02 parts of antioxidant, 02 parts of sulfur resistive agent.

Description

The compound PUR Reactive hot melt adhesives and preparation method thereof of fabric
Technical field
The invention belongs to PUR technical field, is related to a kind of PUR Reactive hot melt adhesives, and in particular to a kind of fabric is compound With PUR Reactive hot melt adhesives and preparation method thereof.
Background technology
Composite material forms one or more layers textile material, non-woven material and other functional materials through bonding fitting A kind of new material.It is adapted to make the textiles such as sofa, clothes, is that people live one of indispensable fabric at home.Fabric is answered Usually using water-based, oiliness or conventional hot melt type adhesive during conjunction.
Reaction type polyurethane hot-melt adhesive is a kind of Novel adhesive to grow up on the basis of traditional hot-melt adhesive.It is main Reacted by PPG or PEPA and diisocyanate etc., generation isocyano containing end(—NCO)Pre-polymerization Body, add the auxiliary agents such as tackifying resin, filler, antioxidant, catalyst and be formulated, using the moisture in performed polymer and air or The reaction of moisture on adherend surface produces preferable adhesion strength.Its reactivity is extremely strong, and using when need to be melted so Coating after compound to forming composite material on weaving face fabric afterwards.In use, terminal isocyanato is because having Very strong reactivity, easily reacted with active hydride, particularly water, the open hour are short, poor storage stability.And solidified Journey pole is also easy to produce CO2, bonding layer is formed random pin hole or foaming, cause film performance to be deteriorated, adhesive strength declines.
The content of the invention
In order to solve the above-mentioned technical problem, the invention provides a kind of fabric compound PUR Reactive hot melt adhesives and its system Preparation Method.
The present invention adopts the following technical scheme that to realize foregoing invention purpose:
Fabric is compound to use PUR Reactive hot melt adhesives, by weight, is made up of following raw material:Toluene di-isocyanate(TDI) 50-70 parts, Crystalline polymer polyalcohol 20-25 parts, end-capping reagent 1-2 parts, tackifying resin 5-15 parts, filler 5-10 parts, carbon black It is 1-5 parts, silica gel 1-5 parts, calcium hydroxide 1-5 parts, coupling agent 0-2 parts, plasticizer 0-2 parts, ultraviolet absorber 0-2 parts, anti-oxidant Agent 0-2 parts, sulfur resistive agent 0-2 parts.
Preferably, by weight, it is made up of following raw material:60 parts of toluene di-isocyanate(TDI), crystalline polymer polyalcohol 22 parts, it is 1.2 parts of end-capping reagent, 8 parts of tackifying resin, 6 parts of filler, 3 parts of carbon black, 2 parts of silica gel, 1.5 parts of calcium hydroxide, even Join 0.5 part of agent, 0.5 part of plasticizer, 1 part of ultraviolet absorber, 1 part of antioxidant, 0.5 part of sulfur resistive agent.
The present invention adds appropriate carbon black, silica gel as adsorbent in formula, and calcium hydroxide is as chemical absorbent; In addition, plasticizer, tackifier, coupling agent, ultraviolet absorber, antioxidant, sulfur resistive agent and filler etc. are incorporated also in glue, significantly Enhance the pliability of Reactive hot melt adhesive, compound fastness, stability and inoxidizability.
When the water content of glued base material is higher, air humidity is larger, sizing material-NCO group content is higher, solidification temperature When higher, curing rate is very fast, is also easy to produce more CO in this case2Gas.CO2Formed bonding layer during effusion random Pin hole or foaming, cause film performance to be deteriorated, adhesive strength decline.Therefore, appropriate carbon black and silica gel are added in formula to make It is adsorbent and calcium hydroxide as chemical absorbent.
Crystalline polymer polyalcohol of the present invention is the polyester diol that molecular weight is 2000-2500.
End-capping reagent of the present invention for it is double-(3- methoxyl group silicon propyl group)Amine.
The compound preparation method with PUR Reactive hot melt adhesives of fabric of the present invention, step are as follows:
1)The crystalline polymer polyalcohol of formula ratio is put into the vacuum dehydration that 3-5h is carried out in 100 DEG C of vacuum drying chamber;
2)50-60 DEG C is cooled to, product is added in reactor, adds toluene di-isocyanate(TDI), is slowly stirred, treats temperature 90-100 DEG C is risen to, is incubated 30-60min, is continuously heating to 100-110 DEG C, end-capping reagent is added, stirring reaction 3-5h, adds Remaining raw material in formula, is stirred, and vacuum removal bubble, produces.
The beneficial effects of the present invention are:
1st, polyurethane terminal isocyanate base is converted into silane oxygen groups by the addition of end-capping reagent, effectively improves end group isocyanic acid Ester group meets the situation that water forms cross-linked gel, improves storage stability, according to silicone cure mechanism during silane oxygen groups film forming, Gu Typically be not in solidification foaming phenomena during change, and end-blocking degree and curing rate possess adjustability.
2nd, the present invention from it is double-(3- methoxyl group silicon propyl group)Amine is as end-capping reagent, and it is active secondary amine base silane, and it possesses Excellent reactivity, and cost is relatively low, and the process of polyurethane prepolymer blocking modification is easily controlled.
3rd, appropriate carbon black is added in being formulated, silica gel is inhaled as adsorbent, calcium hydroxide as chemical absorbent, absorption Receive CO caused by solidification2;In addition, plasticizer, coupling agent, tackifier, ultraviolet absorber, antioxidant, anti-is incorporated also in glue Vulcanizing agent and filler etc., the pliability of Reactive hot melt adhesive, compound fastness, stability and inoxidizability are significantly enhanced, effectively Extend the open hour.
Embodiment
The essentiality content of the present invention is described in further detail with reference to embodiment.
Embodiment 1
Fabric is compound to use PUR Reactive hot melt adhesives, by weight, is made up of following raw material:50 parts of toluene di-isocyanate(TDI), crystallization 20 parts of polymer polyatomic alcohol of property, 1 part of end-capping reagent, 5 parts of tackifying resin, 5 parts of filler, 1 part of carbon black, 1 part of silica gel, hydrogen-oxygen Change 1 part of calcium.
Embodiment 2
Fabric is compound to use PUR Reactive hot melt adhesives, by weight, is made up of following raw material:70 parts of toluene di-isocyanate(TDI), crystallization 25 parts of polymer polyatomic alcohol of property, 2 parts of end-capping reagent, 15 parts of tackifying resin, 10 parts of filler, 5 parts of carbon black, 5 parts of silica gel, hydroxide 5 parts of calcium, 2 parts of coupling agent, 2 parts of plasticizer, 2 parts of ultraviolet absorber, 2 parts of antioxidant, 2 parts of sulfur resistive agent.
Described crystalline polymer polyalcohol is the polyester diol that molecular weight is 2000.
Embodiment 3
Fabric is compound to use PUR Reactive hot melt adhesives, by weight, is made up of following raw material:60 parts of toluene di-isocyanate(TDI), crystallization 23 parts of polymer polyatomic alcohol of property, it is double-(3- methoxyl group silicon propyl group)1.2 parts of amine, 10 parts of tackifying resin, 8 parts of filler, charcoal Black 2 parts, 1.5 parts of silica gel, 2.5 parts of calcium hydroxide, 1 part of coupling agent, 0.5 part of plasticizer, 1.5 parts of antioxidant.
Described crystalline polymer polyalcohol is the polyester diol that molecular weight is 2500.
Embodiment 4
Fabric is compound to use PUR Reactive hot melt adhesives, by weight, is made up of following raw material:60 parts of toluene di-isocyanate(TDI), crystallization 22 parts of polymer polyatomic alcohol of property, it is double-(3- methoxyl group silicon propyl group)1.2 parts of amine, 8 parts of tackifying resin, 6 parts of filler, carbon black 3 parts, 2 parts of silica gel, 1.5 parts of calcium hydroxide, 0.5 part of coupling agent, 0.5 part of plasticizer, 1 part of ultraviolet absorber, 1 part of antioxidant, 0.5 part of sulfur resistive agent.
Described crystalline polymer polyalcohol is the polyester diol that molecular weight is 2200.
In inventive formulation it is double-(3- methoxyl group silicon propyl group)Amine blocks Chemical Co., Ltd. purchased from Hangzhou Jesse.
Embodiment 5
The present embodiment is the preparation method of embodiment 1, and step is as follows:
1)The crystalline polymer polyalcohol of formula ratio is put into the vacuum dehydration that 4h is carried out in 100 DEG C of vacuum drying chamber;
2)50 DEG C are cooled to, product is added in reactor, adds toluene di-isocyanate(TDI), is slowly stirred, is treated in temperature 95 DEG C are risen to, is incubated 60min, is continuously heating to 100 DEG C, adds end-capping reagent, stirring reaction 5h, remaining original added in formula Material, is stirred, vacuum removal bubble, produces.
Embodiment 6
The present embodiment is the preparation method of embodiment 2, and step is as follows:
1)The crystalline polymer polyalcohol of formula ratio is put into the vacuum dehydration that 3h is carried out in 100 DEG C of vacuum drying chamber;
2)60 DEG C are cooled to, product is added in reactor, adds toluene di-isocyanate(TDI), is slowly stirred, is treated in temperature 100 DEG C are risen to, is incubated 30min, is continuously heating to 110 DEG C, adds end-capping reagent, stirring reaction 3h, remaining original added in formula Material, is stirred, vacuum removal bubble, produces.
Embodiment 7
The present embodiment is the preparation method of embodiment 3, and step is as follows:
1)The crystalline polymer polyalcohol of formula ratio is put into the vacuum dehydration that 4h is carried out in 100 DEG C of vacuum drying chamber;
2)55 DEG C are cooled to, product is added in reactor, adds toluene di-isocyanate(TDI), is slowly stirred, is treated in temperature 95 DEG C are risen to, is incubated 50min, is continuously heating to 105 DEG C, adds end-capping reagent, stirring reaction 4h, remaining original added in formula Material, is stirred, vacuum removal bubble, produces.
Embodiment 8
The present embodiment is the preparation method of embodiment 4, and step is as follows:
1)The crystalline polymer polyalcohol of formula ratio is put into the vacuum dehydration that 5h is carried out in 100 DEG C of vacuum drying chamber;
2)50 DEG C are cooled to, product is added in reactor, adds toluene di-isocyanate(TDI), is slowly stirred, is treated in temperature 90 DEG C are risen to, is incubated 60min, is continuously heating to 100 DEG C, adds end-capping reagent, stirring reaction 5h, remaining original added in formula Material, is stirred, vacuum removal bubble, produces.
The apparent viscosity of the PUR Reactive hot melt adhesives of the present invention is 5300MPas, open hour 6min, 24 hours heat endurances It is stable.
The PUR Reactive hot melt adhesives of the present invention are subjected to fabric composite testing, with commercially available adhesive group as a comparison, selected Three kinds of 100D polar fleeces, 55D looped fabrics, 50D spandex fabrics cloth have made three kinds of samples respectively as sample base fabric.To three kinds Sample washes the testing experiment of peel strength after preceding and washing respectively, and result of the test is shown in Table 1:
Table 1 washes the testing experiment result table of peel strength after preceding and washing
From table 1, PUR of the invention washing conservation rate of decaying is substantially better than commercially available prod, will not be in the suds because Bonding intensity declines and produces quality problems.

Claims (5)

1. fabric is compound to use PUR Reactive hot melt adhesives, it is characterised in that:By weight, it is made up of following raw material:Toluene diisocyanate Acid esters 50-70 parts, crystalline polymer polyalcohol 20-25 parts, end-capping reagent 1-2 parts, tackifying resin 5-15 parts, filler 5-10 parts, carbon black 1-5 parts, silica gel 1-5 parts, calcium hydroxide 1-5 parts, coupling agent 0-2 parts, plasticizer 0-2 parts, ultraviolet absorber 0- 2 parts, antioxidant 0-2 parts, sulfur resistive agent 0-2 parts.
2. fabric according to claim 1 is compound to use PUR Reactive hot melt adhesives, it is characterised in that:By weight, by following Raw material forms:60 parts of toluene di-isocyanate(TDI), 22 parts of crystalline polymer polyalcohol, 1.2 parts of end-capping reagent, tackifying resin 8 Part, 6 parts of filler, 3 parts of carbon black, 2 parts of silica gel, 1.5 parts of calcium hydroxide, 0.5 part of coupling agent, 0.5 part of plasticizer, ultraviolet suction Receive 1 part of agent, 1 part of antioxidant, 0.5 part of sulfur resistive agent.
3. fabric according to claim 1 is compound to use PUR Reactive hot melt adhesives, it is characterised in that:Described crystallinity is gathered Compound polyalcohol is the polyester diol that molecular weight is 2000-2500.
4. fabric according to claim 1 is compound to use PUR Reactive hot melt adhesives, it is characterised in that:Described end-capping reagent is Double-(3- methoxyl group silicon propyl group)Amine.
5. the compound preparation method with PUR Reactive hot melt adhesives of fabric according to claim 1, it is characterised in that:Step It is as follows:
1)The crystalline polymer polyalcohol of formula ratio is put into the vacuum dehydration that 3-5h is carried out in 100 DEG C of vacuum drying chamber;
2)50-60 DEG C is cooled to, product is added in reactor, adds toluene di-isocyanate(TDI), is slowly stirred, treats temperature 90-100 DEG C is risen to, is incubated 30-60min, is continuously heating to 100-110 DEG C, end-capping reagent is added, stirring reaction 3-5h, adds Remaining raw material in formula, is stirred, and vacuum removal bubble, produces.
CN201610684921.3A 2016-08-18 2016-08-18 The compound PUR Reactive hot melt adhesives and preparation method thereof of fabric Pending CN107760245A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111423837A (en) * 2020-04-08 2020-07-17 上海抚佳精细化工有限公司 TPU hot melt adhesive and preparation method thereof
CN113150733A (en) * 2021-03-12 2021-07-23 东莞聚力创新材料科技有限公司 Removable reactive polyurethane hot melt adhesive and preparation method thereof

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EP1578830A1 (en) * 2002-12-20 2005-09-28 Bayer MaterialScience LLC Moisture-curable, polyether urethanes with terminal cyclic urea/reactive silane groups and their use as sealants, adhesives and coatings
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CN102492389A (en) * 2011-12-15 2012-06-13 广州市白云化工实业有限公司 Moisture-cured silicone modified polyurethane and hot melt adhesive composition and preparation method thereof
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CN1649928A (en) * 2002-04-09 2005-08-03 拉克西米·C·古普塔 Water curable polyurethane compositions and uses thereof
EP1578830A1 (en) * 2002-12-20 2005-09-28 Bayer MaterialScience LLC Moisture-curable, polyether urethanes with terminal cyclic urea/reactive silane groups and their use as sealants, adhesives and coatings
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CN102492389A (en) * 2011-12-15 2012-06-13 广州市白云化工实业有限公司 Moisture-cured silicone modified polyurethane and hot melt adhesive composition and preparation method thereof
CN105061714A (en) * 2015-08-10 2015-11-18 烟台德邦科技有限公司 Synthetic method and application of silicon alkane terminated polyurethane prepolymer

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111423837A (en) * 2020-04-08 2020-07-17 上海抚佳精细化工有限公司 TPU hot melt adhesive and preparation method thereof
CN113150733A (en) * 2021-03-12 2021-07-23 东莞聚力创新材料科技有限公司 Removable reactive polyurethane hot melt adhesive and preparation method thereof

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Application publication date: 20180306