DE2263922A1 - HOT-MELT ADHESIVES, IN PARTICULAR FOR GLUING TEXTILE MATERIALS - Google Patents

HOT-MELT ADHESIVES, IN PARTICULAR FOR GLUING TEXTILE MATERIALS

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Publication number
DE2263922A1
DE2263922A1 DE2263922A DE2263922A DE2263922A1 DE 2263922 A1 DE2263922 A1 DE 2263922A1 DE 2263922 A DE2263922 A DE 2263922A DE 2263922 A DE2263922 A DE 2263922A DE 2263922 A1 DE2263922 A1 DE 2263922A1
Authority
DE
Germany
Prior art keywords
percent
weight
hot
textile materials
melt adhesives
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.)
Pending
Application number
DE2263922A
Other languages
German (de)
Inventor
Hanns-Dietmar Dr Haertl
Peter Dr Horn
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.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Priority to DE2263922A priority Critical patent/DE2263922A1/en
Priority to BE138217A priority patent/BE807858A/en
Priority to IT54023/73A priority patent/IT1000177B/en
Priority to FR7344349A priority patent/FR2327298A1/en
Priority to GB5851273A priority patent/GB1443768A/en
Publication of DE2263922A1 publication Critical patent/DE2263922A1/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/36Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino acids, polyamines and polycarboxylic acids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04Interconnection of layers
    • B32B7/12Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B5/00Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/22Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed
    • B32B5/24Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer
    • B32B5/26Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer another layer next to it also being fibrous or filamentary
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/59Polyamides; Polyimides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Polyamides (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

Badische Anilin- 4 -Soda-Fabuk AGBadische Anilin- 4 -Soda-Fabuk AG

Unser Zeichen: O.Z. 29 6O8 Ka/IG 6700 Ludvigsbafen, 27.12.1972Our reference: O.Z. 29 6O8 Ka / IG 6700 Ludvigsbafen, December 27, 1972

Schmelzkleber, insbesondere zum Verleimen von textlien MaterialienHotmelt adhesives, in particular for gluing textile materials

Die Erfindung betrifft einen Schmelzkleber auf Basis von Copolyaoiiden zum Verleimen von verschiedenen Materialien, vornehmlich von textlien Haterieüien.The invention relates to a hotmelt adhesive based on Copolyaoiiden for gluing different materials, mainly from textlien haterieüien.

Aus der belgischen Patentschrift 752 668 und der deutschen Auslegeschrift 1 253 449 ist es bereits bekannt, Copolyamide auf Basis 65-Aminoundecansäure einerseits und Laurinlactam andererseits 31Hn Verkleben von Textilien zu verwenden. Diese Schmelzkleber auf Basis von 60-Aminoundecansäure und Laurinlaotam sind jedoch neben anderen Mangeln mit dem Nachteil behaftet, daß die zu ihrer Herstellung erforderlichen Ausgangsmaterialien schwer zugänglich sind.From Belgian patent specification 752 668 and German Auslegeschrift 1 253 449 it is already known to use copolyamides based on 65-aminoundecanoic acid on the one hand and laurolactam on the other hand 3 1 Hn bonding of textiles. However, these hot-melt adhesives based on 60-aminoundecanoic acid and laurollaotam have the disadvantage, along with other deficiencies, that the starting materials required for their production are difficult to access.

Überraschenderweise wurde nun gefunden, daß man unter Verwendung der genannten Nachteile gemäß der Erfindung Schmelzkleber auf Basis von Copolyamiden erhält, die sich durch hohe Klebefestigkeit, geringe Wasseraufnahme, gute Waschbeständigkeit gegen Seifenlaugen und Beständigkeit gegenüber bestimmten organischen Lösungsmitteln, insbesondere chlorierten Kohlenwasserstoffen auszeichnen.Surprisingly, it has now been found that, using the disadvantages mentioned, according to the invention, hot-melt adhesives based on copolyamides, which are characterized by high adhesive strength, low water absorption, good wash resistance against soapy water and resistance to certain organic solvents, especially chlorinated solvents Label hydrocarbons.

Die erfindungsgemäßen Schmelzkleber sind dadurch gekennzeichnet, daß sie aus Copolyamiden aus 20 bis 40 Gewichtsprozent 6-Caprolactam, 10 bis 30 Gewichtsprozent Adipinsäure - Hexanethylendiaminsalz und 30 bis 50 Gewichtsprozent Dodecandisäure - ac, 62-Diaminsalz bestehen, cc, (*> -Diamine im Sinne der Erfindung sind aliphatische, bzw. cycloaliphatische Diamine, beispielsweise Hexamethylendiamin, Trishexamethylendiamin, 4 ,4 '-Diaminodicyclohexylmethaii und 2,2,4-Trimethylhexamethylendiamin. Die Produkte eignen sich in Pulverform besonders zum Verleimen von Textilien .in der Hitze.The hot-melt adhesives according to the invention are characterized in that they consist of copolyamides of 20 to 40 percent by weight 6-caprolactam, 10 to 30 percent by weight adipic acid - hexanethylenediamine salt and 30 to 50 percent by weight dodecanedioic acid - ac, 62-diamine salt, cc, (*> -diamine in the sense of the invention are aliphatic or cycloaliphatic diamines, for example hexamethylenediamine, trishexamethylenediamine, 4,4'-diaminodicyclohexylmethaii and 2,2,4-trimethylhexamethylenediamine.The products are particularly suitable in powder form for gluing textiles in the heat.

696/72 409832/0904 - 2 -696/72 409832/0904 - 2 -

- ? '- ο. ζ. 29 6οδ- ? '- ο. ζ. 29 6οδ

Die Hersteilung der Copolyamide wird vorteilhafterweise so durchgeführt, daß das Copolyamid einen Kondensationsgrad aufweist, der einem K-Wert nach Pikentscher (1-gewichtsprozentig in konzentrierter Schwefelsäure) von 40 bis 65 entspricht. Der Kondensationsgrad kann durch Zugabe eines Kettenreglers wie z.B. einer monofunktionellen Carbonsäure, z.B. Stearinsäure bzw. Propionsäure, vor der Polykondensation eingestellt werden,The preparation of the copolyamides is advantageous carried out so that the copolyamide has a degree of condensation which has a K value according to Pikentscher (1 percent by weight in concentrated sulfuric acid) from 40 to 65. The degree of condensation can be adjusted by adding a Chain regulator such as a monofunctional carboxylic acid, e.g. stearic acid or propionic acid, before the polycondensation be set,

Die Erfindung ist nachstehend anhand eines Beispiels näher erläutert.The invention is explained in more detail below using an example.

Beispielexample

a) Herstellung des Copolyamids a) Production of the copolyamide

In einen Druckautoklaven von 350 1 Inhalt wurdenIn a pressure autoclave of 350 1 content were

40 kg t-Caprolactam40 kg of t-caprolactam

40 kg Dodecandisäure/Hexamethylendiamin-Salz40 kg dodecanedioic acid / hexamethylenediamine salt

20 kg Adipinsäure/Hexamethylendiamin-Salz20 kg of adipic acid / hexamethylenediamine salt

1,5 kg Stearinsäure1.5 kg of stearic acid

10 kg VE-Wasser10 kg of deionized water

gegeben. Zur Vorkondensation wurde auf 27O0C unter Eigendruck (20 atü) erhitzt und das Reaktionsgemisch 1 Stunde bei dieser Temperatur gehalten» Anschließend wurde innerhalb von 2 Stunden auf Normaldruck entspannt. Zur Nachkondensation wurde das Reaktionsgemisch weitere 2 Stunden im Stickstoffstrom auf 27O0C erhitzt. Das getrocknete Granulat wies einen K-Wert (1-gewichtsprozentig in konzentrierter Schwefelsäure) von 56 und einen Meltindex von 55 g/10 Minuten bei 1900C auf.given. For the pre-condensation (20 atm) was heated to 27O 0 C under autogenous pressure the reaction mixture is heated and "held for 1 hour at this temperature then was depressurized within 2 hours at atmospheric pressure. For post-condensation, the reaction mixture was heated an additional 2 hours in a nitrogen stream at 27O 0 C. The dried granules had a K value (1 percent by weight in concentrated sulfuric acid) of 56 and a melt index of 55 g / 10 minutes at 190 0 C.

b) Messung der Klebefestigkeit b) Measurement of the adhesive strength

Die Herstellung des Probekörpers geschieht folgendermaßen: Ein textiles Gewebe, z.B. aus Pasern aus Polyäthylenterephthalat, wird auf einer Fläche von 400 cm mit dem Copolyamid in der Weise imprägniert, daß man einen 0,3 mm dickenThe test specimen is produced as follows: A textile fabric, e.g. made of fibers made of polyethylene terephthalate, is impregnated on an area of 400 cm with the copolyamide in such a way that a 0.3 mm thick

A09832/0904 " 3 "A09832 / 0904 " 3 "

- 3 - . O.Z. 29 6o8- 3 -. O.Z. 29 6o8

Film des Copolyamide auf das textile Gewebe mit einem Druck bis zu 200 atü bei Temperaturen zwischen 140 und 20O0C aufpreßt. Auf dieses mit dem Copolyamid imprägnierte Gewebe wird bei einem Druck bis zu höchstens 5 atü proThe film of the copolyamide is pressed onto the textile fabric with a pressure of up to 200 atmospheres at temperatures between 140 and 20O 0 C. This fabric, which is impregnated with the copolyamide, is applied at a pressure of up to a maximum of 5 atmospheres per hour

400 cm ein unbehandeltes Gewebe aus gleichem Textilmaterial bei Temperaturen zwischen 140 bis 1800C aufkaschiert. Die Festigkeit wird in bekannter Weise durch Auseinanderziehen der beiden Textilgewebe, das in 5 cm breite Streifen geschnitten wurde, bestimmt«400 cm an untreated fabric made of the same textile material at temperatures between 140 to 180 0 C laminated. The strength is determined in a known manner by pulling apart the two textile fabrics, which were cut into 5 cm wide strips «

Das erfindungsgemäß verwendete Copolyamid verleiht der kaschierten Textilprobe eine Festigkeit von ca. 10 Kp pro 5 cm Breite.The copolyamide used according to the invention imparts the laminated textile sample has a strength of approx. 10 Kp per 5 cm width.

c) Bestimmung der Trockenreinigungsbeständigkeit c) Determination of dry cleaning resistance

Die unter b) beschriebenen kaschierten Textiiproben wurden einer Trockenreinigung durch 5maliges Waschen mit Perchloräthylen unterzogen, was einen Festigkeitsabfall von nur ca. 5 bewirkte.The laminated textile samples described under b) were subjected to dry cleaning by washing 5 times with perchlorethylene, which caused a drop in strength of only about 5 ° .

d) Waschbeständigkeit gegenüber Seifenlaugen d) Resistance to washing in soapy water

Die unter b) beschriebenen kaschierten Textiiproben wurden einem 5maligen Waschtest von jeweils 45 Minuten Dauer bei 600C unterzogen. Als Seifenlauge diente eine 0,7gewichtsprozentige wäßrige Seifenlösung» Die Klebefestigkeit der kasdierten Probe nimmt dabei nur um den vergleichsweise geringen Betrag von ca. 10 $ ab οThe laminated textile samples described under b) were subjected to a 5maligen washing test of 45 minutes duration at 60 0 C. A 0.7% by weight aqueous soap solution was used as the soapy water

A09832/0904A09832 / 0904

Claims (2)

- 4 - ο. ζ. 29 6o8 Patentansprüche- 4 - ο. ζ. 29 6o8 claims 1. Schmelzkleber auf der Basis von Copolyamiden, insbesondere für textile Materialien, bestehend aus einem Copolyamid aus 20 bis 40 Gewichtsprozent 6-Caprolactam, 10 bis 30 Gewichtsprozent Adipinsäure - Hexamethylendiaminsalz und 35 bis 50 Gewichtsprozent Dodecandisäure - et, to -Diaminsalz.1. Hotmelt adhesive based on copolyamides, especially for textile materials, consisting of a copolyamide from 20 to 40 percent by weight 6-caprolactam, 10 to 30 percent by weight Adipic acid - hexamethylenediamine salt and 35 to 50 percent by weight dodecanedioic acid - et, to -diamine salt. 2. Schmelzkleber nach Anspruch 1, dadurch gekennzeicnnet, daß das Copolyamid einen K-Wert nach Fikentscher (lgewichtsprozentig in konzentrierter Schwefelsäure) von 40 bis 65 aufweist. 2. Hotmelt adhesive according to claim 1, characterized in that the copolyamide has a Fikentscher K value (weight percent in concentrated sulfuric acid) of 40 to 65. Badische Anilin- & Soda-Fabrik AGBadische Anilin- & Soda-Fabrik AG 409832/09CH409832 / 09CH
DE2263922A 1972-12-29 1972-12-29 HOT-MELT ADHESIVES, IN PARTICULAR FOR GLUING TEXTILE MATERIALS Pending DE2263922A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
DE2263922A DE2263922A1 (en) 1972-12-29 1972-12-29 HOT-MELT ADHESIVES, IN PARTICULAR FOR GLUING TEXTILE MATERIALS
BE138217A BE807858A (en) 1972-12-29 1973-11-27 FUSE ADHESIVES ESPECIALLY SUITABLE FOR BONDING TEXTILE MATERIALS
IT54023/73A IT1000177B (en) 1972-12-29 1973-11-30 FUSIBLE ADHESIVES IN PARTICULAR FOR BONDING TEXTILE MATERIALS
FR7344349A FR2327298A1 (en) 1972-12-29 1973-12-12 FUSE ADHESIVES ESPECIALLY SUITABLE FOR BONDING TEXTILE MATERIALS
GB5851273A GB1443768A (en) 1972-12-29 1973-12-18 Hot-melt adhesives used for gluing materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2263922A DE2263922A1 (en) 1972-12-29 1972-12-29 HOT-MELT ADHESIVES, IN PARTICULAR FOR GLUING TEXTILE MATERIALS

Publications (1)

Publication Number Publication Date
DE2263922A1 true DE2263922A1 (en) 1974-08-08

Family

ID=5865691

Family Applications (1)

Application Number Title Priority Date Filing Date
DE2263922A Pending DE2263922A1 (en) 1972-12-29 1972-12-29 HOT-MELT ADHESIVES, IN PARTICULAR FOR GLUING TEXTILE MATERIALS

Country Status (5)

Country Link
BE (1) BE807858A (en)
DE (1) DE2263922A1 (en)
FR (1) FR2327298A1 (en)
GB (1) GB1443768A (en)
IT (1) IT1000177B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0306794A2 (en) 1987-09-09 1989-03-15 Ems-Inventa Ag Copolyamide adhesive

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1098877C (en) * 2000-12-15 2003-01-15 中国船舶重工集团公司第七研究院第七○四研究所 High-molecular material for stern bearing of ship

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0306794A2 (en) 1987-09-09 1989-03-15 Ems-Inventa Ag Copolyamide adhesive
EP0306794A3 (en) * 1987-09-09 1990-10-24 Ems-Inventa Ag Copolyamide adhesive

Also Published As

Publication number Publication date
FR2327298A1 (en) 1977-05-06
FR2327298B1 (en) 1978-03-24
IT1000177B (en) 1976-03-30
GB1443768A (en) 1976-07-28
BE807858A (en) 1974-05-27

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