EP4041837A1 - Ruban adhésif - Google Patents

Ruban adhésif

Info

Publication number
EP4041837A1
EP4041837A1 EP20775235.3A EP20775235A EP4041837A1 EP 4041837 A1 EP4041837 A1 EP 4041837A1 EP 20775235 A EP20775235 A EP 20775235A EP 4041837 A1 EP4041837 A1 EP 4041837A1
Authority
EP
European Patent Office
Prior art keywords
carrier
adhesive tape
velor
adhesive
tape according
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Withdrawn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
EP20775235.3A
Other languages
German (de)
English (en)
Inventor
René RAMBUSCH
Timo Leermann
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.)
Certoplast Technische Klebebander GmbH
Original Assignee
Certoplast Technische Klebebander GmbH
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 Certoplast Technische Klebebander GmbH filed Critical Certoplast Technische Klebebander GmbH
Publication of EP4041837A1 publication Critical patent/EP4041837A1/fr
Withdrawn legal-status Critical Current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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16Dicarboxylic acids and dihydroxy compounds
    • C08G63/18Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
    • C08G63/181Acids containing aromatic rings
    • C08G63/183Terephthalic acids
    • 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
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/21Paper; Textile fabrics
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • 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
    • C09J2203/00Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/302Applications of adhesives in processes or use of adhesives in the form of films or foils for bundling cables
    • 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
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/10Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/16Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the structure of the carrier layer
    • 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
    • C09J2400/00Presence of inorganic and organic materials
    • C09J2400/20Presence of organic materials
    • C09J2400/26Presence of textile or fabric
    • C09J2400/263Presence of textile or fabric in the substrate
    • 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
    • C09J2467/00Presence of polyester
    • C09J2467/006Presence of polyester in the substrate
    • 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
    • C09J2477/00Presence of polyamide
    • C09J2477/006Presence of polyamide in the substrate

Definitions

  • the invention relates to an adhesive tape, in particular a winding tape for sheathing cables in automobiles, with a predominantly textile carrier and with an adhesive coating applied to one or both sides of the carrier, the textile carrier being wholly or partly made of bio-based polymer fibers and / or polymer threads .
  • Adhesive tapes and, in particular, wrapping tapes for sheathing cables in automobiles are used to combine the cables in question or also to protect them from mechanical abrasion.
  • media resistance to, for example, oil and gasoline but also the required temperature resistance are of great importance.
  • such adhesive tapes and in particular wrapping tapes are typically used in the temperature range between -50 ° C. up to +150 ° C. and more.
  • additional sound emissions are aimed at. Also increased abrasion resistance to prevent the body from chafing.
  • the abrasion resistance of the adhesive tape can be determined based on the standard LV 312 (2009) using abrasion classes. Details on this and on the test methods used are described, inter alia, in DE 20 2012 103 975 U1.
  • abrasion class B corresponds to the fact that the adhesive tape in question withstands at least 100 strokes until it is worn through, when it is stuck on a 5 millimeter mandrel, taking into account a weight load of 10 N.
  • the required resistance to abrasion, media and temperature there is often also the requirement that the adhesive tape or wrapping tape in question must be able to be torn manually.
  • the wrapping tapes in question are typically wrapped around the cable bundle to be appropriately equipped by an assembly worker. This can be done in a spiral or helical manner.
  • a so-called longitudinal sheathing of the cable bundle to be equipped with this can also be implemented with the aid of such an adhesive tape or also a wrapping tape.
  • the processing often requires the adhesive tape to be cut to length, which in the simplest case is done by simply tearing it off.
  • hand tearability is of particular importance, which is given or can be given by way of example and in accordance with the explanations in DE 600 31 332 T2 if the adhesive tape has a tear strength in the transverse direction of less than 10N. Basically, hand tearability can also simply and simply be assessed subjectively on the basis of tests.
  • the textile carrier is at least partially based on bio-based polymers is made.
  • the textile carrier can be made from bio-based polymer fibers and / or polymer threads.
  • Nonwovens, knitted fabrics, woven fabrics or combinations are mentioned as possibilities for such a textile carrier. This has basically proven itself, but still offers room for further improvements, in particular to the effect that adhesive tapes with reduced noise emissions are made available.
  • the invention is based on the technical problem of further developing such an adhesive tape and in particular winding tape for sheathing cables in automobiles in such a way that all application-specific requirements in connection with resource-saving production are met and rattling noises are effectively suppressed at the same time.
  • the invention proposes, in the context of the invention, for a generic adhesive tape and, in particular, wrapping tape for sheathing cables in automobiles, that the predominantly textile carrier is designed as a velor carrier or contains one.
  • the carrier is predominant, i. H. More than 50% by mass, textile, but can also contain non-textile components such as foils, which accordingly make up less than 50% by mass or weight of the carrier.
  • the invention therefore first and foremost falls back on a special textile carrier which is made entirely or partially from the bio-based polymer fibers and / or polymer threads.
  • the textile carrier is designed overall as a velor carrier.
  • the predominantly textile-based carrier can in principle also be designed as a laminate, that is to say as a multi-layer carrier. While in The former case where the carrier is single-layer and is formed solely from the velor carrier, the variant of the carrier designed as a laminate corresponds to the carrier being multi-layered, with at least one layer of the carrier representing a velor carrier.
  • the remaining layers can be textile and non-textile layers as long as the mass or weight fraction of the textile components of the carrier is more than 50% of its total mass or its total weight.
  • the procedure can be, for example, that the carrier is designed as a laminate and, in addition to the velor carrier, also has a film carrier.
  • the carrier is finally made in two layers and is composed on the one hand of the velor carrier and on the other hand the film carrier. It has proven useful here if the film carrier is arranged between the velor carrier and the adhesive coating.
  • the velor carrier with its velor loops has an arrangement such that the velor loops of the velor carrier point outwards.
  • the adhesive coating is applied on the opposite side of the adhesive tape to the film carrier, which in turn is arranged between the adhesive coating and the velor carrier.
  • the film carrier can be designed as a bio-based polymer film carrier.
  • the film carrier is designed as a biopolyester film carrier, that is to say is produced as a film carrier based on biopolyester.
  • the biopolyester is advantageously designed as a bio-based PET (polyethylene terephthalate).
  • the basic building blocks of this bio-based polymer are made from renewable raw materials instead of crude oil.
  • the renewable raw materials can be those based on vegetable materials such as starchy plants.
  • such bio-based polymers can also be produced using lactic acid.
  • the bio-based polymer film or the bio-based polymer film carrier and in particular the biopolyester film carrier can be realized and implemented in such a way that, in the example, PET is produced by polycondensation from monoethylene glycol (or ethylene glycol) and terephthalic acid.
  • the monoethylene glycol can be produced from sugar cane molasses.
  • Terephthalic acid can be produced bio-based or petrochemically.
  • the velor backing with its velor loops advantageously pointing outwards, ensures that the adhesive tape and in particular wrapping tape implemented in this way can not only be produced in a particularly resource-saving manner, but also has particular advantages with regard to any noise emissions.
  • the outward-facing velor loops effectively dampen any rattling noises. This means that the velor loops are found on the upper side of the adhesive tape pointing outwards, whereas the adhesive coating is regularly present on the opposite inside.
  • the adhesive layer points inwards or ensures that the adhesive tape is fixed on the cable bundle or cable harness, so that the velor loops as part of the velor backing automatically point outwards and so for that
  • the necessary noise suppression and, in particular, the suppression of any rattling noises This is where the main advantages can be seen.
  • the velor loops pointing outwards typically have a loop length in the range from 0.5 mm to 5 mm and in particular 0.8 mm to 2 mm.
  • a loop length has proven to be particularly favorable and practicable, because on the one hand the velor loops do not protrude significantly from the adhesive tape and thus any entanglements with screws, edges or other sharp-edged projections in the interior of the motor vehicle are avoided.
  • the specified length spectrum for the velor loops is sufficient to achieve effective noise damping at the same time.
  • the velor carrier generally has a mesh density of more than 5000 per dm 2 , in particular the mesh density is in the range from about 25,000 per dm 2 to 50,000 per dm 2 .
  • This design provides a dense surface and the corresponding velor loops ensure a particularly large-area noise-dampening effect.
  • the velor carrier is generally a knitted fabric velor carrier with the velor loops facing outwards.
  • the velor loops usually form an outer bar in a velvet weave, for example. In principle, a super velvet binding is also possible in this context. In addition to this outer bar with a velvet weave or super velvet weave, an inner bar with a tricot weave can also be realized underneath.
  • the velor loops are advantageously knitted not only into the outer bar, but also into the inner bar below. Filaments or filament threads based on polyamide or polyester are typically used to produce the velor backing. Since bio-based polymer threads are mostly taken into account in this context, the velor backing is made entirely of filaments based on bio-polyamide or bio-polyester.
  • the biopolyester for the production of the filaments of the velor carrier is advantageously PET, which in turn is produced in a manner comparable to the PET for the production of the film carrier.
  • PET the monoethylene glycol required for this can be produced from sugar cane molasses.
  • the additionally required terephthalic acid may in turn be produced petrochemically or bio-based. This means that raw materials comparable to those used for the filaments for the manufacture of the velor carrier are used for the optional film carrier.
  • the velor backing is made from filaments based on biopolyamide.
  • the invention further recommends that the monomers or amines of the bio-polyamide consist entirely or in part of castor oil.
  • the additionally required acid or carboxylic acid can in turn be produced in a manner comparable to terephthalic acid for PET, predominantly petrochemically, but recently also bio-based. In principle, mixed forms are also conceivable.
  • the predominantly textile carrier can be configured as a single layer, in which case the textile carrier is designed solely as a velor carrier.
  • the carrier can also be designed in multiple layers.
  • the carrier is advantageously designed in two layers and is composed on the one hand of the outwardly facing velor carrier and on the other hand the film carrier to which the adhesive coating is applied.
  • the carrier typically has a basis weight in Range from 20 g / m 2 to 500 g / m 2 .
  • the thickness or material thickness of the carrier is usually between 0.5 mm and 3 mm in order to ensure good processability.
  • the adhesive coating is then applied either to the back of the velor carrier or the inner bar or to the interposed film carrier.
  • An application weight in the range from 20 g / m 2 to 500 g / m 2 has proven to be particularly favorable here.
  • a synthetic rubber adhesive, a hotmelt adhesive, an adhesive based on acrylate, an adhesive based on silicone, polyurethane, polyether and / or polyolefin are used, for example, as the adhesive.
  • the adhesive can in principle be crosslinked after the coating, in particular by radiation crosslinking.
  • the adhesive coating can be applied to the carrier over the entire surface or in strips.
  • an adhesive tape and in particular a wrapping tape for sheathing cables in automobiles is made available, which can be produced in a particularly resource-saving manner.
  • the predominantly textile carrier is wholly or partially made from bio-based polymer fibers and / or polymer threads.
  • filament threads are used at this point, i.e. continuous fibers made from the bio-based polymer.
  • the bio-based polymer is usually one based on bio-polyamide or bio-polyester.
  • the velor backing is made from filaments based on biopolyamide.
  • adhesive tapes can be produced which at least achieve abrasion class B and predominantly even abrasion class C or even D according to LV 312 (2009), as already described above has been.
  • the adhesive tape produced in this way can be torn by hand, with tear strengths in the transverse direction of the adhesive tape of typically 20 N and in particular even 10 N being observed, taking into account an adhesive tape width in the range up to approx. 50 mm.
  • the carrier is predominantly based on biopolyamide or biopolyester, not only are the abrasion resistances already described above achieved, but such a carrier is also distinguished by high media and temperature resistance. In connection with the special soundproofing ability achieved by the outwardly standing velor loops, the requirements necessary for the chosen application are met.
  • the fineness of the filaments based on biopolyamide for the realization of the velor backing is usually between 20 dtex and 100 dtex.
  • the abrasion resistance be set as high as described, but the elongation at break of the carrier material can also be specified so that it is in the range between 30% and 70%.
  • the tear strength of the entire adhesive tape is typically in the range from about 100 N / cm to 200 N / cm, specifically in the longitudinal direction of the adhesive tape. In the transverse direction of the adhesive tape, tear strengths that are lower by a factor of 10 are observed at this point, which are achieved, for example, by making perforations in the carrier in the transverse direction. This usually happens before the adhesive coating is applied.
  • FIG. 1 shows an adhesive tape which is used as a wrapping tape for bundling or sheathing cables in automobiles.
  • a predominantly textile carrier which is a velor carrier 1
  • the velor carrier 1 is equipped with an adhesive coating 2.
  • the adhesive coating 2 covers the velor carrier 1 at least in some areas and can consequently be applied over the entire surface or in strip form.
  • a film carrier 3 is provided between the adhesive coating 2 and the velor carrier 1.
  • the velor carrier 1 has velor loops 4 facing outwards.
  • the velor loops 4 primarily take over the sound insulation and form an outer bar 5.
  • the outer bar 5 has a velvet weave.
  • an inner bar 6 in a tricot weave according to the exemplary embodiment is also provided, which is arranged in the direction of the film carrier 3 between the outer bar 5 and the said film carrier 3.
  • Both the velor carrier 1 and the film carrier 3 are each made bio-based, as was previously described in detail.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesive Tapes (AREA)
  • Laminated Bodies (AREA)
  • Package Frames And Binding Bands (AREA)
  • Knitting Of Fabric (AREA)

Abstract

L'invention concerne un ruban adhésif, en particulier une bande d'emballage, de gainage de câbles d'automobile, ayant un support principalement textile et au moins une couche de revêtement adhésive appliquée sur un côté ou les deux côtés du support textile, et le support textile étant fabriqué entièrement ou partiellement à partir de fibres polymères à base biologique et/ou de fils polymères, caractérisé en ce que le support textile est un support velours ou comprend un tel support textile.
EP20775235.3A 2019-10-11 2020-09-16 Ruban adhésif Withdrawn EP4041837A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE202019105633.9U DE202019105633U1 (de) 2019-10-11 2019-10-11 Klebeband
PCT/EP2020/075833 WO2021069185A1 (fr) 2019-10-11 2020-09-16 Ruban adhésif

Publications (1)

Publication Number Publication Date
EP4041837A1 true EP4041837A1 (fr) 2022-08-17

Family

ID=68886578

Family Applications (1)

Application Number Title Priority Date Filing Date
EP20775235.3A Withdrawn EP4041837A1 (fr) 2019-10-11 2020-09-16 Ruban adhésif

Country Status (5)

Country Link
US (1) US20230065871A1 (fr)
EP (1) EP4041837A1 (fr)
CN (1) CN114555738A (fr)
DE (1) DE202019105633U1 (fr)
WO (1) WO2021069185A1 (fr)

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2797268B1 (fr) 1999-08-02 2002-03-22 Scapa Tapes France S A Ruban adhesif sur tissu de polyester dechirable a la main
DE50102233D1 (de) * 2000-03-22 2004-06-17 Certoplast Vorwerk & Sohn Gmbh Klebeband
US20070173156A1 (en) * 2004-03-04 2007-07-26 Tesa Ag Highly abrasion-resistant tape for binding cable trees in motor vehicles
DE202012103442U1 (de) * 2012-09-10 2012-09-28 Certoplast Vorwerk & Sohn Gmbh Klebeband, insbesondere Wickelband zur Bündelung von Kabeln in Automobilen
DE202012103975U1 (de) 2012-10-17 2014-02-06 Coroplast Fritz Müller Gmbh & Co. Kg Hoch abriebfestes technisches Klebeband mit doppellagigem Träger
DE102013223495A1 (de) * 2013-11-18 2015-05-21 Tesa Se Klebeband zum Ummanteln von langgestrecktem Gut wie insbesondere Kabelsätzen und Verfahren zur Ummantelung
FI11757U1 (fi) 2017-06-30 2017-08-21 Pelloplast Oy Pintasuojakalvo
DE202019100588U1 (de) 2019-01-31 2019-02-07 Certoplast Technische Klebebänder Gmbh Klebeband, insbesondere Wickelband

Also Published As

Publication number Publication date
US20230065871A1 (en) 2023-03-02
DE202019105633U1 (de) 2019-11-27
CN114555738A (zh) 2022-05-27
WO2021069185A1 (fr) 2021-04-15

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