EP1151053A1 - Klebstoffpulver - Google Patents

Klebstoffpulver

Info

Publication number
EP1151053A1
EP1151053A1 EP99960999A EP99960999A EP1151053A1 EP 1151053 A1 EP1151053 A1 EP 1151053A1 EP 99960999 A EP99960999 A EP 99960999A EP 99960999 A EP99960999 A EP 99960999A EP 1151053 A1 EP1151053 A1 EP 1151053A1
Authority
EP
European Patent Office
Prior art keywords
adhesive powder
powder according
substrate
room temperature
adhesive
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP99960999A
Other languages
German (de)
English (en)
French (fr)
Inventor
Michael Kalbe
Silke Wagener
Peter Grynaeus
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Carl Freudenberg KG
Original Assignee
Carl Freudenberg KG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Carl Freudenberg KG filed Critical Carl Freudenberg KG
Publication of EP1151053A1 publication Critical patent/EP1151053A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • C09J9/00Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks
    • 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
    • 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
    • C09J201/00Adhesives based on unspecified macromolecular compounds
    • 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
    • C09J5/00Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
    • C09J5/06Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers involving heating of the applied adhesive
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • 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
    • C09J2463/00Presence of epoxy resin

Definitions

  • the invention relates to the production of an adhesive powder for joining flat, closed or porous substrates, the adhesive powder being applied to a first substrate in a first step and an intermediate product which is not tacky at room temperature being produced, and a joining being carried out in the second step the first substrate with a second substrate by using elevated temperature and pressure.
  • Adhesive powders based on thermoplastics which can be applied to the substrate to be bonded and give a non-tacky, storage-stable intermediate product, are generally known.
  • the connection to a second substrate is made by applying heat under pressure and the adhesive layer is solidified physically by cooling.
  • the disadvantage of these hot melt or heat seal adhesives is that the temperature resistance of the composite produced by the The melting range of the thermoplastic used is limited. In some composites, the low melting point of the copolymers and the associated low crystallinity also reduce the hydrolysis and solvent stability of the composite.
  • the invention has for its object to provide an adhesive powder which can be applied to a first substrate, with the substrate at room temperature forms a firm connection and is stable in storage.
  • This intermediate product which is non-adhesive at room temperature and is stable in storage, is said to be able to be bonded to a second substrate in the lowest possible temperature range and at low pressures.
  • the response time should therefore be as short as possible.
  • the object is achieved in the case of an adhesive powder of the type mentioned at the outset by the combination of the following constituents.
  • the powder consists of a thermoplastic polymer with a proportion of 25 to 95% by weight and at least one epoxy resin which is solid at room temperature with a proportion of 5 to 75% by weight and optionally at least one pre-adduct of epoxy resins and polyamines which is also solid at room temperature with a proportion of at most 25% by weight.
  • adhesive powder When the adhesive powder is applied to the first substrate in a first step, adhesive powder is predominantly physically attached to the substrate, while the two substrates are connected in the second step by chemical crosslinking or post-crosslinking of the powder constituents and subsequent cooling.
  • the mixture of the selected compounds thus enables the production of a non-tacky, storage-stable substrate with an adhesive layer which, when applied to the substrate, primarily connects to the substrate in a physical manner.
  • the adhesive layer After the cooling process, the adhesive layer is latently reactive. In the lamination process with a second substrate at a higher temperature than in the application process on the first substrate, the adhesive layer is activated and crosslinking takes place.
  • the product produced has improved temperature and hydrolysis and solvent stability compared to purely thermoplastic adhesives and also has improved elasticity compared to products with epoxy-based adhesives. The reason for this is a crosslinking of the polymer with the epoxy resin. It was also surprising that the crosslinking of the components begins at significantly lower temperatures. Depending on the composition of the adhesive powder, crosslinking could be achieved from 90 ° C. Networking also took place with an extremely short reaction time.
  • the proportion of the thermoplastic polymer can vary within wide ranges, but a proportion of 50 to 90% by weight is preferred.
  • the amount of epoxy resin is significantly less. It is preferably 10 to 50% by weight. In the event that a pre-adduct is used, its proportion is at most 25% by weight.
  • thermoplastic polymers are low-melting polyamides, polyesters, polyurethanes and / or vinyl copolymers with the functional side groups carboxyl, amino, amido and anhydro. It is also possible that the thermoplastic polymer is a polymer blend of low-melting polyamides, polyesters, polyurethanes and / or vinyl copolymers with the functional side groups carboxyl, amino, amido, anhydro.
  • the polymers are made up of linear or branched monomers.
  • the polyamide can be formed from one or more of the following monomers:
  • the polyester is created from one or more of the following monomers:
  • At least one ⁇ -hydroxy carboxylic acid At least one lactone.
  • the polyurethanes can be composed of diisocyanates, polyols and diols.
  • Epoxy resins which are solid at room temperature preferably have reaction products of epichlorohydrin with bisphenol A and / or reaction products Epichlorohydrin with bisphenol F. It is also possible that the epoxy resin has polyfunctional epoxides. This includes, for example, epoxidized novolaks.
  • the pre-adduct of epoxy resins and polyamines which is also solid at room temperature, consists of reaction products of epoxy resins based on bisphenol A and polyamine and / or reaction products of epoxy resins based on bisphenol F and polyamine.
  • a pre-adduct of epoxy resins and polyaminoamides from polyamines and dimeric fatty acids is also possible.
  • the adhesive powder is mixed with other additives.
  • Suitable additives are low-melting resins and / or waxes with melting points below 100 ° C., preferably below 90 ° C. and / or dyes and / or mineral and / or organic fillers. The total proportion of these additives should not exceed 10% by weight.
  • the use of low-melting resins and / or waxes is particularly suitable if the application process to the first substrate is to take place at the lowest possible temperatures. Dyes have an influence on the coloring. Metallic fillers have an influence on the thermal conductivity. Your weight percentage can be higher.
  • thermoplastic polymer or the epoxy resin have a first melting point which is different from the other two components and is below 130 ° C., preferably below 100 ° C., and a softening point between 50 and 90 ° C. This ensures that during the application process on a first substrate only by surface melting of the thermoplastic polymer or the epoxy resin, a connection to the substrate takes place, while the other component (s) are not yet melting. This means that the melting point of the other two components is higher than the first melting point of the thermoplastic polymer or epoxy resin. It turns out, however, that the second melting point of the other component (s) need only be slightly above the first melting point in order to achieve good results. Epoxy resins are therefore used whose melting point is below 130 ° C., preferably below 100 ° C. This contributes significantly to the fact that the energy requirement for the bonding of the two substrates is kept as low as possible.
  • the application temperature at which the powder is applied to the substrate is usually 5 to 10 ° C above the melting point of the component with the lowest melting point.
  • the adhesive powder it is also possible for the adhesive powder to be fixed on the first substrate at the first elevated temperature by melting the additives. The bonding of the adhesive layer on the first substrate takes place here purely physically. Only when the two substrates are joined together with a second raised one
  • the grain size of the adhesive powder is chosen to be less than 200 ⁇ m, preferably less than 100 ⁇ m.
  • the second substrate is also provided with the adhesive powder in a first step. If necessary, this can support the gluing process during lamination.
  • a powder mixture made of a thermoplastic, a polyamide, an epoxy resin, a polyamine-epoxy pre-addulate, a wax and an amorphous silicon dioxide is produced in a stirred tank.
  • the weight fractions in the above order are 64.6%; 27.6; 5.3; 2.0; 0.5.
  • a product with the trade name Platamid H 103PA80 is selected as polyamide and a product with the name Epikote 1002 as epoxy resin.
  • the individual components are ground to a grain size of less than 100 ⁇ m.
  • the mixture prepared in this way is mixed with water and a paste base consisting of dispersant, running aid and thickener to form a paste and applied to one side of a nonwoven in the coating process. Then a drying temperature of 95 ° C is applied.
  • the nonwoven fabric provided with the adhesive powder shows a good one Storage stability. The nonwoven webs wound into rolls did not stick together, the adhesive powder adheres firmly to the surface of the nonwoven.
  • the nonwoven fabric produced in this way was placed on a woolen fabric and passed together with it through a continuous press using pressure and heat.
  • the press temperature was 120 ° C with a press pressure of 3 bar and a residence time of 30 seconds.
  • the laminate produced in this way was extremely durable in the sense of the task.
  • a powder produced in the same way with a polyamide content of 62.5% by weight, an epoxy content of 32.5% by weight (Epikote 1055) and a wax with 4% by weight is treated with 1% by weight of silicon dioxide
  • Processing aids and water and paste base processed into a paste The paste is applied to a nonwoven fabric at room temperature and dried in a continuous oven at 105 ° C.
  • the nonwoven fabric had good storage stability.
  • the lamination process was carried out at a press temperature of 130 ° C.
  • the laminate produced showed high temperature resistance and solvent stability.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Laminated Bodies (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
EP99960999A 1998-12-07 1999-11-25 Klebstoffpulver Withdrawn EP1151053A1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19856254 1998-12-07
DE19856254A DE19856254A1 (de) 1998-12-07 1998-12-07 Klebstoffpulver
PCT/EP1999/009098 WO2000034406A1 (de) 1998-12-07 1999-11-25 Klebstoffpulver

Publications (1)

Publication Number Publication Date
EP1151053A1 true EP1151053A1 (de) 2001-11-07

Family

ID=7890155

Family Applications (1)

Application Number Title Priority Date Filing Date
EP99960999A Withdrawn EP1151053A1 (de) 1998-12-07 1999-11-25 Klebstoffpulver

Country Status (13)

Country Link
US (1) US6515048B1 (es)
EP (1) EP1151053A1 (es)
JP (1) JP2002531679A (es)
KR (1) KR100491844B1 (es)
CN (1) CN1329651A (es)
AR (1) AR020018A1 (es)
AU (1) AU1776800A (es)
DE (1) DE19856254A1 (es)
HU (1) HUP0105051A3 (es)
RU (1) RU2221699C2 (es)
TR (1) TR200101657T2 (es)
TW (1) TW502057B (es)
WO (1) WO2000034406A1 (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10338967B4 (de) * 2003-08-25 2007-02-22 Technische Universität Braunschweig Carolo-Wilhelmina Verfahren zum Kleben von Mikrobauteilen auf ein Substrat
CN101284265B (zh) * 2007-04-13 2010-09-08 欧利速精密工业股份有限公司 热熔黏胶粉末用于非金属物体表面的处理方法及处理装置
DE102007026724A1 (de) * 2007-06-06 2008-12-11 Basf Coatings Japan Ltd., Yokohama Bindemittel mit hoher OH-Zahl und sie enthaltende Klarlackzusammensetzungen mit guten optischen Eigenschaften und guter Kratz- und Chemikalienbeständigkeit
BR112013026588A2 (pt) * 2011-04-15 2016-12-27 Fuller H B Co adesivos à base de difenilmetano-di-isocianato modificado
EP2653486B1 (en) * 2012-04-20 2014-12-03 3M Innovative Properties Company Low density epoxy composition with low water uptake
DE102012216500A1 (de) * 2012-09-17 2014-03-20 Hp Pelzer Holding Gmbh Mehrlagiger gelochter Schallabsorber
CN104231204B (zh) * 2014-09-18 2017-08-29 东莞市吉鑫高分子科技有限公司 一种太阳能电池用热塑性聚氨酯弹性体及其制备方法
BR112018006395B1 (pt) * 2015-10-26 2022-05-31 Dow Global Technologies Llc Composição adesiva e laminado
US20190292427A1 (en) * 2016-05-19 2019-09-26 Zephyros, Inc. Hot melt applicable structural adhesives
DE112019005171T5 (de) * 2018-10-16 2021-09-16 Cummins Filtration Ip, Inc. Klebstofflegierungen und filtermedien einschliesslich solcher klebstofflegierungen
CN113980618B (zh) * 2021-10-28 2022-11-04 横店集团东磁股份有限公司 一种在电感成型压制过程中预防粉料粘模的粘接剂及其压制方法

Family Cites Families (13)

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Publication number Priority date Publication date Assignee Title
US4113684A (en) * 1976-12-10 1978-09-12 Westinghouse Electric Corp. Low temperature cure epoxy-amine adhesive compositions
CH606253A5 (es) * 1977-01-07 1978-10-31 Ciba Geigy Ag
CH606252A5 (es) 1977-01-07 1978-10-31 Ciba Geigy Ag
EP0074218B1 (en) * 1981-08-26 1985-11-13 Raychem Limited Heat recoverable article
US4517340A (en) 1982-08-25 1985-05-14 Raychem Corporation Adhesive composition
GB8403823D0 (en) * 1984-02-14 1984-03-21 Raychem Ltd Adhesive composition
JPS61231066A (ja) * 1985-04-06 1986-10-15 Fujikura Kasei Kk 異方導電性ホツトメルト接着剤
JPS61266483A (ja) * 1985-05-20 1986-11-26 Toagosei Chem Ind Co Ltd 接着剤組成物
JPS63118391A (ja) * 1986-11-06 1988-05-23 Tokyo Ink Kk 接着方法
EP0289632A1 (en) 1987-05-04 1988-11-09 American Cyanamid Company High green strength induction curable adhesives
JP3330390B2 (ja) * 1992-06-11 2002-09-30 三井化学株式会社 ホットメルト接着剤組成物
JPH09328668A (ja) * 1996-06-10 1997-12-22 Sekisui Chem Co Ltd 室温硬化型樹脂組成物、室温硬化型接着剤、反応性ホットメルト型接着剤及び室温硬化型粘着剤
JPH10251612A (ja) * 1997-03-17 1998-09-22 Toppan Printing Co Ltd ホットメルト接着剤組成物およびそれを用いた構造体

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0034406A1 *

Also Published As

Publication number Publication date
TW502057B (en) 2002-09-11
DE19856254A1 (de) 2000-06-08
JP2002531679A (ja) 2002-09-24
HUP0105051A3 (en) 2004-04-28
RU2221699C2 (ru) 2004-01-20
AR020018A1 (es) 2002-03-27
HUP0105051A2 (hu) 2002-04-29
TR200101657T2 (tr) 2001-12-21
AU1776800A (en) 2000-06-26
KR20010089552A (ko) 2001-10-06
CN1329651A (zh) 2002-01-02
US6515048B1 (en) 2003-02-04
KR100491844B1 (ko) 2005-05-27
WO2000034406A1 (de) 2000-06-15

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