EP2408615A1 - Éléments adhérents comportant une couche d'adhésif - Google Patents
Éléments adhérents comportant une couche d'adhésifInfo
- Publication number
- EP2408615A1 EP2408615A1 EP10710307A EP10710307A EP2408615A1 EP 2408615 A1 EP2408615 A1 EP 2408615A1 EP 10710307 A EP10710307 A EP 10710307A EP 10710307 A EP10710307 A EP 10710307A EP 2408615 A1 EP2408615 A1 EP 2408615A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- layer
- foam
- composite element
- cover layer
- element 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- Withdrawn
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 32
- 239000007767 bonding agent Substances 0.000 title abstract description 7
- 239000006260 foam Substances 0.000 claims abstract description 71
- 239000004831 Hot glue Substances 0.000 claims abstract description 28
- 239000007788 liquid Substances 0.000 claims abstract description 21
- 239000007787 solid Substances 0.000 claims abstract description 17
- 238000004519 manufacturing process Methods 0.000 claims abstract description 11
- 239000010410 layer Substances 0.000 claims description 120
- 239000004814 polyurethane Substances 0.000 claims description 25
- 239000002318 adhesion promoter Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 17
- 229920000582 polyisocyanurate Polymers 0.000 claims description 16
- 229920002635 polyurethane Polymers 0.000 claims description 13
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 238000012546 transfer Methods 0.000 claims description 6
- 239000012790 adhesive layer Substances 0.000 claims description 5
- 238000005187 foaming Methods 0.000 claims description 5
- 239000011495 polyisocyanurate Substances 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 238000004132 cross linking Methods 0.000 claims description 4
- 239000004033 plastic Substances 0.000 claims description 4
- 239000000835 fiber Substances 0.000 claims description 3
- 239000005011 phenolic resin Substances 0.000 claims description 3
- 229920001568 phenolic resin Polymers 0.000 claims description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 2
- 238000007766 curtain coating Methods 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- 239000002987 primer (paints) Substances 0.000 description 23
- 239000000463 material Substances 0.000 description 20
- 229910000831 Steel Inorganic materials 0.000 description 13
- 239000010959 steel Substances 0.000 description 13
- 229920002396 Polyurea Polymers 0.000 description 12
- 238000001816 cooling Methods 0.000 description 7
- -1 polyethylenes Polymers 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000004604 Blowing Agent Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 238000000576 coating method Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000012943 hotmelt Substances 0.000 description 4
- 230000037452 priming Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
- 239000003380 propellant Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000005338 heat storage Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000013615 primer Substances 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- 238000003848 UV Light-Curing Methods 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229920013640 amorphous poly alpha olefin Polymers 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920006147 copolyamide elastomer Polymers 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052756 noble gas Inorganic materials 0.000 description 1
- 150000002835 noble gases Chemical class 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229960004624 perflexane Drugs 0.000 description 1
- ZJIJAJXFLBMLCK-UHFFFAOYSA-N perfluorohexane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F ZJIJAJXFLBMLCK-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- ZUFQCVZBBNZMKD-UHFFFAOYSA-M potassium 2-ethylhexanoate Chemical compound [K+].CCCCC(CC)C([O-])=O ZUFQCVZBBNZMKD-UHFFFAOYSA-M 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000003847 radiation curing Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000007420 reactivation Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
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- B32—LAYERED PRODUCTS
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- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
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- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/065—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of foam
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- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
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- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
- B32B27/304—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl halide (co)polymers, e.g. PVC, PVDC, PVF, PVDF
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- B32B5/18—Layered 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 features of a layer of foamed material
- B32B5/20—Layered 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 features of a layer of foamed material foamed in situ
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- B32B5/00—Layered 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
- B32B5/22—Layered 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
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered 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
- B32B5/22—Layered 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
- B32B5/24—Layered 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
- B32B5/245—Layered 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 being a foam layer
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- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B9/00—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00
- B32B9/002—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00 comprising natural stone or artificial stone
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B9/00—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00
- B32B9/005—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00 comprising one layer of ceramic material, e.g. porcelain, ceramic tile
-
- B—PERFORMING OPERATIONS; TRANSPORTING
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B9/00—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00
- B32B9/04—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00 comprising such particular substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B9/045—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00 comprising such particular substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B9/00—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00
- B32B9/04—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00 comprising such particular substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B9/046—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00 comprising such particular substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material of foam
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/02—Synthetic macromolecular fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/10—Inorganic fibres
- B32B2262/108—Rockwool fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2266/00—Composition of foam
- B32B2266/02—Organic
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2266/00—Composition of foam
- B32B2266/02—Organic
- B32B2266/0214—Materials belonging to B32B27/00
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2266/00—Composition of foam
- B32B2266/02—Organic
- B32B2266/0214—Materials belonging to B32B27/00
- B32B2266/0278—Polyurethane
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2266/00—Composition of foam
- B32B2266/02—Organic
- B32B2266/0214—Materials belonging to B32B27/00
- B32B2266/0285—Condensation resins of aldehydes, e.g. with phenols, ureas, melamines
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2266/00—Composition of foam
- B32B2266/08—Closed cell foam
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2266/00—Composition of foam
- B32B2266/10—Composition of foam characterised by the foam pores
- B32B2266/104—Micropores, i.e. with average diameter in the range from 0.1 µm to 0.1 mm
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
Definitions
- the present invention relates to composite elements and their preparation.
- Composite elements e.g., sandwich panels
- a core of foamed material e.g., PIR, PUR, phenolic resin
- the foamed materials can usually form some adhesion to the cover layers during the foaming and curing process, this is for later use of the composite materials - e.g. as components - not always sufficient. Therefore, the cover layers are provided in part before the application of the foamed material with a primer.
- the materials used for the core are foamed in situ by applying a 2K reactive mixture to a topcoat. Due to the chemical reaction of the two components of the reactive mixture, this foams up and begins to cure within a few minutes.
- Adhesion promoters are generally 2K systems which are also used at room temperature. These are advantageously adjusted so that they are not cured when contacted with the intumescent material and can thus enter into a chemical compound with this.
- EP-A 1 516 720 describes composite elements with a foam layer in which a two-component polyurethane adhesive is used as adhesion-promoting layer.
- a primer layer for adhesion promotion between a polyisocyanurate or polyurethane foam and a metal top plate is also described in WO-A 99/00559.
- An object of the present invention is thus to provide such composite elements with adhesion promoters.
- a composite element having a first and a second cover layer, wherein between the first and second cover layer is a foam layer and the interface between the foam layer and at least one cover layer has a primer layer, wherein the primer layer is a hot-liquid, solid at room temperature hot melt adhesive contains.
- a (one-component) hot-liquid, solid at room temperature hot melt adhesive in contrast to the known from the prior art two-component systems has advantageous properties without the adhesion promoter properties are adversely affected. For example, no reactivation of the primer or primer system is required. Furthermore, no errors in the mixing ratio, such as in 2-component systems occur. Complete hardening of the bonding agent layer is always ensured (cooling), regardless of the process conditions of the 2K mixing and dosing system when using a hotmelt adhesive. The same applies to the chemical post-crosslinking in reactive hot melt adhesives, which is ensured either by diffusion of atmospheric moisture in the interface surface layer / primer (adhesion promoter) or by reaction with the reactive constituents of the applied foam mixtures.
- the reaction begins immediately with the merging of the two components.
- the 2K system reacts chemically within a few minutes, especially if it is a 2K PU system as a bonding agent.
- a hot-liquid, solid at room temperature hot melt adhesive needed after
- the physical strength structure (cooling) is not necessarily a further chemical reaction to build strength, but it can advantageously chemically ausureagieren to achieve a higher heat resistance, but this is done over a longer period.
- Typical polyurethane-based or polyolefin-based hot melt adhesives require several days for this. This longer process window has a positive effect on the production process in such a way that the production of a composite element can even be carried out at least partially discontinuously.
- the time window in which chemical reactions with the foam layer are possible substantially longer.
- the (reactive) hot melt adhesive systems are solid for a short time after application, but still have a long time reactivity to the foam layer (see above).
- the provided with primer coatings are thus much easier to handle (no bleeding, dripping down of the primer).
- hot melt adhesives do not require harmful aerosols and are therefore to be preferred in terms of occupational safety and health protection.
- Hot-liquid, solid at room temperature hot melt adhesives are known in the art as such. They are often called “hot melts” or “hotmelts”. As the name suggests, such substances serve as adhesives and are suitable and known for example in the packaging industry for bonding paper or in the furniture and wood industry, for example as a laminate and bookbinding. Reactive hotmelts are sold, for example, as PUR-SK series by the company Klebchemie M.G. Becker GmbH & Co. KG, Weingarten (Germany).
- Such hot melts are often based on polyamides, polyethylenes, amorphous poly- ⁇ -olefins, ethylene-vinyl acetate copolymers, polyesters, polyurethane, polyolefins or copolyamide elastomers.
- an adhesion action of the adhesion promoter layer is not exclusive physical hardening (cooling). Rather, it is preferred if the hot melt adhesive additionally hardens by chemical reaction.
- the adhesion promoter layer may also contain further adhesion-promoting agents (acrylates, silanes, etc.). Preferably, however, the adhesion promoter layer consists exclusively of the hotmelt adhesive. If the second cover layer also has an adhesion promoter layer, this may be the same as or different from that for the first cover layer. Preferably, however, at
- Adhesion promotion for both outer layers used the same adhesive layer material. This is especially true in the event that the material of the first and second
- a particularly preferred adhesion promoter layer in the context of the present invention comprises a polymer or consists of a polymer based on a moisture-crosslinking polyurethane.
- the term "contains” should also include the case that the primer layer consists solely of the hot melt adhesive.
- the term "hot-liquid” means that the material is applied in a liquid state at least to the first cover layer.
- the material should be solid at room temperature.
- the strength at room temperature is achieved on the one hand by cooling and can also be further promoted by chemical reaction with the environment in addition.
- cooling with the reaction of isocyanate groups present in the polymer with ambient humidity can contribute to further crosslinking of the polymer and thus to solidification.
- radiation curing - such as UV curing - can be carried out for corresponding systems.
- the polymers used in the present invention typically have a melting point in the range of 50 to 200 0 C.
- Suitable foam layers are known in the art. These can already be applied as such or generated in situ on a cover layer.
- PIR polyisocyanurates
- PU polyurethanes
- phenolic resins to call.
- PIRs are used, as described, for example, in EP-A 1 516 720.
- the foam layer is a generally known polyisocyanurate foam which is preferably used as a heat-insulating layer in the
- the polyisocyanurate foam forming the foam layer can be obtained, for example, by reacting components a) polyisocyanates with b) compounds which are reactive towards isocyanates, in the presence of c)
- reaction ratio is chosen so that in the reaction mixture, the ratio of the number of isocyanate groups to the number of isocyanate-reactive groups 1.8 to 8: 1, preferably 1.9 to 4: 1.
- the isocyanurate catalyst c) used are generally the isocyanurate group-forming catalysts known from the prior art, preferably alkali metal salts, such as potassium octoate and / or potassium acetate, alone or in combination with tertiary amines.
- alkali metal salts such as potassium octoate and / or potassium acetate
- the Isocyanurat Guess preferably takes place at temperatures above 60 0 C.
- blowing agent (d) As propellant (d) generally so-called physical blowing agents and optionally water are used. Physical blowing agents are understood as meaning compounds which are dissolved or emulsified in the starting materials of the polyurethane preparation and evaporate under the conditions of polyurethane formation. These are, for example, hydrocarbons, halogenated hydrocarbons, and other compounds, such as perfluorinated alkanes, such as perfluorohexane, chlorofluorocarbons, and ethers, esters, ketones and / or acetals. In addition, it is possible to dissolve inert gases, such as nitrogen, carbon dioxide or noble gases under pressure in the polyurethane building components.
- inert gases such as nitrogen, carbon dioxide or noble gases under pressure in the polyurethane building components.
- the blowing agent (d) is generally used in an amount such that the resulting polyisocyanurate foams have a density of from 20 to 300 g / l, preferably from 30 to 100 g / l, particularly preferably from 35 to 80 g / l.
- the PIR foam is a
- Rigid foam i. the foam has a compressive stress at 10% compression or compressive strength according to DIN 53 421 / DIN EN ISO 604 greater than or equal to 100 kPa.
- the rigid foam generally has a DIN ISO 4590 on a Closed cell size of greater 85%, preferably greater than 90%.
- the PIR foam preferably has an average cell diameter of from 10 to 600 ⁇ m, preferably from 50 to 400 ⁇ m, measured according to ASTM 3576-77.
- the adhesion promoter layer has an average layer thickness in the range from 1 to 500 ⁇ m; More preferably in the range of 20 to 250 microns; More preferably in the range of 20 to 120 microns and more preferably in a range of 20 to less than 50 microns, such as 45 microns or 40 microns.
- the term "average layer thickness" in the context of the present invention means that the thickness of the layer can vary and it is sufficient for the purposes of the present invention if the layer thickness averaged over the entire area lies within the stated range. However, it is preferred that no full area application takes place, so that partial areas occur at which the layer is interrupted. Nevertheless, preferably on average, the strength ranges given above should be fulfilled.
- first and second cover layers are basically all commonly used, flexible and rigid cover layers, such as metals such as aluminum, steel, in particular pre-primed steel sheets (coil coating sheets), bitumen, paper, mineral nonwovens, nonwoven fabrics containing organic fibers, plastic (eg Polystyrene, PVC, GRP, ABS), plastic films (eg PE film), wood panels, stone, ceramics or mixtures or laminates thereof, can be used.
- metals such as aluminum, steel, in particular pre-primed steel sheets (coil coating sheets), bitumen, paper, mineral nonwovens, nonwoven fabrics containing organic fibers, plastic (eg Polystyrene, PVC, GRP, ABS), plastic films (eg PE film), wood panels, stone, ceramics or mixtures or laminates thereof, can be used.
- plastic eg Polystyrene, PVC, GRP, ABS
- plastic films eg PE film
- wood panels eg stone, ceramics or mixtures or laminates thereof
- First and second cover layers may be the
- Another object of the present invention is a method for producing a composite element according to the invention comprising the steps
- the adhesion promoter layer is physically solidified on its surface before step (c) and, in particular, that the material is no longer able to flow due to the cooling process, but the crystallization process necessary for the final physical strength build-up has not yet been completed. This has the advantage that a problem-free application of the components for the foam layer is possible.
- the adhesion promoter layer cures completely chemically after step (d), ie after completion of the composite element. This allows a longer process window for the production of the composite element according to the invention.
- An advantage of the hot-liquid room temperature solid hot melt adhesive for the present invention is that it is applied in a liquid state. As a result, a simplification in handling when applying the adhesive layer compared to 2K systems is possible. This also avoids overspray, which is often associated with 2K systems with aerosol formation and represents a significant occupational hygiene disadvantage.
- the primer layer for the present invention may preferably be applied in a simple manner by means of a roller, a doctor blade, a slot die, curtain coating or by spraying (in thread form). Such a step can be easily incorporated into the existing composite element manufacturing facility. A special handling of the cover layers to be coated is not required in principle.
- the material for the primer layer is first applied to a transfer agent, which in turn applies the layer or material formed on the top surface.
- the transfer means may be one or more rolls or one or more strips or combinations thereof.
- the order for the transfer means i. the application of the hot-liquid material
- the order for the transfer means is separated in time from the generation of the primer layer, if necessary, for example, to allow a cooling or certain tempering.
- the material for the primer layer is applied in a hot liquid state.
- the temperature of the material during application is preferably in the range from 80 ° C. to 190 ° C. It is further preferred that the temperature is in the range from 100 ° C. to 130 ° C.
- the temperature may also assume higher values, for example up to 220 ° 0 C, wherein preferably the application to the cover layer, however, takes place in the above-mentioned temperature range.
- non-reactive hot melt adhesives may require higher application temperatures of up to 280 ° C because of their chemical and physical properties.
- steps (b) and (c) take place in discontinuous mode of operation in the method according to the invention for producing a composite element.
- it can be done both a continuous and a discontinuous driving.
- continuous driving is preferred.
- the discontinuous driving style It is possible to design the production of cover layers provided with a primer layer as an endless belt analogous to existing coil coating processes or else the temporal and / or spatial separation of the application of the adhesion promoter layer from the application of the foam or its components also a high flexibility with regard to the selected blowing agent for the foam (n-, i-, cyclo-pentane, 365mfc, 245fa, 134a, formic acid, water).
- the selected blowing agent for the foam n-, i-, cyclo-pentane, 365mfc, 245fa, 134a, formic acid, water.
- step (d) of the method according to the invention the foam layer is brought into contact with the second cover layer.
- This can be done, in particular, by bringing the second cover layer into contact by foaming the foam layer.
- the second cover layer can also be supplied by application to the foam layer or bringing into contact takes place both by applying the second cover layer and by foaming the foam layer.
- first and second cover layers wherein at least one of the two cover layers has a primer layer containing a hot-liquid, solid at room temperature hot melt adhesive, so that a gap between the first and second cover layer occurs, and in this space the Foam layer-forming components introduces and can foam.
- a further subject of the present invention is therefore a method for producing a composite element according to the invention comprising the steps
- This method is particularly suitable for a discontinuous driving style.
- Preferred embodiments correspond to those for the above-mentioned likewise inventive method.
- the bonding agent layer is physically solidified on its surface prior to introduction of the components of the foam layer. It is likewise advantageous if the bonding agent layer hardens completely chemically after step (b). Also applies to the application of the primer layer, the above.
- the composite element according to the invention can be used, for example, as a thermal insulation element, i. used as a composite element for thermal insulation, as proposed in EP-A 1 516 720. Accordingly, a thermal conductivity of the composite element is preferred which is less than 35 mW / mK, more preferably less than 25 mW / mK, measured according to DIN 52612 Part 1.
- the layers of the composite element according to the invention have the following average layer thicknesses.
- the cover layers independently have an average layer thickness of 200 ⁇ m to 5 mm, preferably 300 ⁇ m to 2 mm, particularly preferably 400 ⁇ m to 1 mm.
- the foam layer preferably has an average layer thickness of from 2 cm to 25 cm, preferably from 2.5 cm to 20 cm, particularly preferably from 3 cm to 15 cm.
- KLEIBERIT PUR SK 703.5 Application of the KLEIBERIT PUR SK 703.5 to steel sheet prior to introducing the PUR or PIR foam improves the adhesion of the foam to the steel sheet.
- the manual lifting test leads to a partial adhesion loss of the foam to the steel sheet without prior application of the KLEIBERIT PUR SK 703.5.
- Test specimens with spray-on KLEIBERIT PUR SK 703.5 show a full-surface material breakage of the foam. To lift the foam higher forces are required compared to non-pretreated steel sheets.
- KLEIBERIT PUR SK 703.5 Application of the KLEIBERIT PUR SK 703.5 to steel sheet before introducing the PUR or PIR foam improves the adhesion of the foam to the steel sheet.
- the manual lifting test leads to a partial adhesion loss of the foam to the steel sheet without prior application of the KLEIBERIT PUR SK 703.5.
- Test specimens with spray-on KLEIBERIT PUR SK 703.5 show a full-surface material breakage of the foam. To lift the foam higher forces are required compared to non-pretreated steel sheets.
- the two examples demonstrate that a primer PURSK the adhesion between steel and foam in the two very critical cases of an n-pentane-driven PIR foam Example 1 and a pure water-driven PIR foam with high index Example 2 so far improved that instead a loss of adhesion steel foam a material break in the foam is observed. That is, the adhesion exceeds the cohesion of the foam.
Landscapes
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Laminated Bodies (AREA)
Abstract
La présente invention concerne un élément adhérent comprenant une première et une seconde couche de protection et comportant, entre ces deux couches de protection, une couche de mousse, l'interface entre la couche de mousse et l'une au moins des couches de protection comportant quant à elle une couche d'adhésif. En l'occurrence, l'élément adhérent de l'invention est caractérisé en ce que la couche d'adhésif contient une colle fondue qui est liquide à chaud et qui prend à température ambiante. L'invention concerne également un procédé de fabrication d'un tel produit.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009013712A DE102009013712A1 (de) | 2009-03-20 | 2009-03-20 | Verbundelemente mit Haftvermittlerschicht |
| PCT/EP2010/053695 WO2010106189A1 (fr) | 2009-03-20 | 2010-03-22 | Éléments adhérents comportant une couche d'adhésif |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2408615A1 true EP2408615A1 (fr) | 2012-01-25 |
Family
ID=42167290
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP10710307A Withdrawn EP2408615A1 (fr) | 2009-03-20 | 2010-03-22 | Éléments adhérents comportant une couche d'adhésif |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP2408615A1 (fr) |
| DE (1) | DE102009013712A1 (fr) |
| WO (1) | WO2010106189A1 (fr) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102012017529A1 (de) * | 2012-09-04 | 2014-03-06 | Gottlieb Binder Gmbh & Co. Kg | Abdecksystem für Isolationseinrichtungen an Bau- und Tragwerken |
| DE102015117201A1 (de) | 2015-10-08 | 2017-04-13 | Bwg Bergwerk- Und Walzwerk-Maschinenbau Gmbh | Verfahren und Anlage zum kontinuierlichen Herstellen von Verbundbändern oder -blechen |
| DE102018005393A1 (de) * | 2018-07-09 | 2020-01-09 | Fahrzeugwerk Bernard Krone GmbH & Co. KG | Verfahren zur Herstellung von Sandwich-Paneelen für insbesondere Nutzfahrzeugaufbauten von Kühlfahrzeugen |
| US11794450B2 (en) | 2020-12-18 | 2023-10-24 | Altria Client Services Llc | Polymer-laminated metal lid |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3236313A1 (de) * | 1982-09-30 | 1984-04-05 | H.B. Fuller GmbH, 8000 München | Schmelzklebstoff |
| DE4101806A1 (de) * | 1991-01-23 | 1992-07-30 | Basf Ag | Schockabsorbierende propylenpolymer-verbundformteile |
| DE4109397A1 (de) | 1991-03-22 | 1992-09-24 | Agrodur Grosalski & Co | Verfahren zur herstellung eines metall-kunststoffverbundes |
| DE4419449A1 (de) * | 1994-06-03 | 1995-12-07 | Henkel Kgaa | Schnell abbindender Polyurethan-Schmelzklebstoff |
| US6096416A (en) | 1997-06-26 | 2000-08-01 | Altenberg; Milton J. | Metal sandwich panels |
| FR2772778B1 (fr) * | 1997-12-19 | 2002-03-29 | Ato Findley Sa | Adhesif polyurethane reticulable par l'humidite, procede de collage d'un textile et d'un materiau cellulaire au moyen dudit adhesif et assemblage colle ainsi obtenu |
| TW200305587A (en) * | 2002-03-19 | 2003-11-01 | Rohm & Haas | Urethane polymer compositions |
| DE10258431B4 (de) * | 2002-12-13 | 2008-03-06 | National Starch & Chemical Gmbh & Co. Kg | Haus- oder Wohnungseingangstür |
| DE10343902A1 (de) | 2003-09-19 | 2005-05-19 | Basf Ag | Verbundelement, enthaltend einen Polyurethanhaftvermittler |
| JP4381941B2 (ja) * | 2004-09-17 | 2009-12-09 | 王子インターパック株式会社 | 自動車内装天井材用の積層部材 |
| DE102006058257A1 (de) * | 2006-12-08 | 2008-06-19 | Julius Heywinkel Gmbh | Verbundbauelement sowie Verfahren zum Herstellen eines Verbundbauelementes, insbesondere für den Automobilbau |
| EP2060378A1 (fr) * | 2007-11-14 | 2009-05-20 | Alcan Technology & Management Ltd. | Procédé de fabrication d'un matériau composite |
-
2009
- 2009-03-20 DE DE102009013712A patent/DE102009013712A1/de not_active Withdrawn
-
2010
- 2010-03-22 WO PCT/EP2010/053695 patent/WO2010106189A1/fr not_active Ceased
- 2010-03-22 EP EP10710307A patent/EP2408615A1/fr not_active Withdrawn
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2010106189A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| DE102009013712A1 (de) | 2010-09-23 |
| WO2010106189A1 (fr) | 2010-09-23 |
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