WO2002079304A2 - Verfahren zur herstellung von verbundfolien mit einem lösungsmittelfreien klebersystem - Google Patents
Verfahren zur herstellung von verbundfolien mit einem lösungsmittelfreien klebersystem Download PDFInfo
- Publication number
- WO2002079304A2 WO2002079304A2 PCT/EP2002/003558 EP0203558W WO02079304A2 WO 2002079304 A2 WO2002079304 A2 WO 2002079304A2 EP 0203558 W EP0203558 W EP 0203558W WO 02079304 A2 WO02079304 A2 WO 02079304A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- film
- adhesive
- composite
- composite film
- films
- Prior art date
Links
Classifications
-
- 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
- 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
- B32B27/08—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 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
- B32B27/00—Layered products comprising a layer of synthetic resin
- 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
-
- 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
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
-
- 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
- B32B7/00—Layered 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
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/73—Polyisocyanates or polyisothiocyanates acyclic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/12—Bonding of a preformed macromolecular material to the same or other solid material such as metal, glass, leather, e.g. using adhesives
- C08J5/124—Bonding of a preformed macromolecular material to the same or other solid material such as metal, glass, leather, e.g. using adhesives using adhesives based on a macromolecular component
- C08J5/128—Adhesives without diluent
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/06—Polyurethanes from polyesters
-
- 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
- B32B38/00—Ancillary operations in connection with laminating processes
- B32B2038/0052—Other operations not otherwise provided for
- B32B2038/0092—Metallizing
-
- 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
- B32B2250/00—Layers arrangement
- B32B2250/24—All layers being polymeric
-
- 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
- B32B2307/70—Other properties
- B32B2307/724—Permeability to gases, adsorption
- B32B2307/7242—Non-permeable
- B32B2307/7244—Oxygen barrier
-
- 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
- B32B2307/70—Other properties
- B32B2307/724—Permeability to gases, adsorption
- B32B2307/7242—Non-permeable
- B32B2307/7246—Water vapor barrier
-
- 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
- B32B2327/00—Polyvinylhalogenides
-
- 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
- B32B2367/00—Polyesters, e.g. PET, i.e. polyethylene terephthalate
Definitions
- the present invention relates to a method for producing composite films by means of a solvent-free adhesive system, in particular composite films with barrier properties, and to composite films obtainable by this method.
- packaging materials with a wide variety of property profiles are required in the packaging industry.
- the packaging material used may be permeable to gases such as, for example, oxygen, nitrogen, carbon dioxide and moisture, or to have a reduced permeability or impermeability.
- Packaging materials with barrier properties should in particular be able to preserve the atmosphere contained or intended in the packaging, for example a nitrogen protective gas atmosphere, in order to be able to guarantee the quality of the packaging goods even over a longer period of time.
- Such materials are also intended to prevent the penetration of oxygen and / or moisture into the packaging, which could spoil the goods.
- packaging materials used should be as inexpensive as possible. This requires corresponding economic manufacturing processes.
- BESTATIGUNGSKOPIE In order to increase the barrier properties of films, two or more films are glued together to form a composite film, an adhesive with barrier properties being used as the adhesive. Thus, according to the invention, double, triple, quadruple composite films and composite films with more than 4 films can be obtained.
- Adhesive systems which are preferably used are solvent-free, since the energy-intensive removal of solvents, which requires additional work steps and is therefore expensive, is eliminated, as is the case in conventional solvent-based adhesive systems.
- a solvent-free adhesive system based on polyurethane for the production of composite films with barrier properties, which comprises a polyester resin with hydroxyl groups as the first adhesive component and a diisocyanate as the second hardener component.
- the polyester resin having hydroxyl groups is obtained by reacting a linear aliphatic diol having two to ten carbon atoms with a linear dicarboxylic acid, n-butanediol and N-hexanediol being the preferred diols and adipic acid being the preferred dicarboxylic acid.
- the polyester resin used is in crystalline form at room temperature and has a melting point of about 80 ° or less, with lower melting polyester resins being preferred.
- the number average molecular weight of the polyester component is between 300 and 5,000, preferably between 500 and 2,000.
- the hydroxyl number of the polyester resin component is stated to be about 20 to about 350, preferably about 100 to about 250. Due to the low melting point of the polyester resin, the adhesive system can also be used at the low temperatures that are required to prevent deformation or other impairment of the polymer films due to the high temperature.
- Aliphatic, preferably linear, but also aromatic diisocyanates are mentioned as the diisocyanate component.
- the two components of the adhesive system are heated to the lamination temperature and applied to the first film immediately before the second film is laminated on. To fully harden the composite film obtained, it is recommended to store it for at least one week afterwards.
- the films described in the working examples show good barrier properties with regard to oxygen permeability and, in one case, for moisture permeability.
- aromatic diisocyanates as adhesive components or to replace them with aliphatic ones.
- US 4,496,417 describes a laminating device for connecting a plastic film to a reinforcing material made of paper.
- the adhesive is simultaneously applied to both the plastic film and the paper web during the lamination process, the lamination process also being able to take place with cooling.
- the method according to the invention enables the post-curing time of the finished composite films to be shortened.
- the object of the invention is achieved by a method for producing composite films by gluing a first film to a second film by means of a solvent-free adhesive system, the adhesive system being preheated to the application temperature in a first stage, in a second stage, the adhesive system preheated to the application temperature, if appropriate after mixing individual adhesive system components, is applied to the first film, and in a third step the first film coated with the adhesive system is connected to an incoming second film with cooling.
- adhesive systems based on aliphatic, in particular aliphatic linear, diisocyanates can be used to obtain composite films with excellent barrier properties economically and without problems.
- this process can shorten the curing time of the films to a few days.
- Temperature logistics has proven to be a decisive factor for the method according to the invention, in particular adequate preheating of the adhesive system or its components, ensuring the application of the adhesive system to the first film at the application temperature required for the materials used, and cooling of the first film during the lamination of the second film.
- the total amount of the adhesive system that is applied to the first film should have a temperature that is as constant and uniform as possible.
- the individual adhesive components are therefore preheated over a period of time which is sufficient to ensure that the temperature of the components used is as uniform as possible.
- the accuracy and uniformity of the application temperature achieved by the above measures guarantees the accuracy of the viscosity of the adhesive system and thus a uniform quality of the adhesive application.
- the risk of nonsense is avoided, that is to say the spraying of adhesive system applied to the film.
- the second film is bonded to the first film provided with the adhesive system while cooling the first film.
- the laminating roller, over which the first film runs during the connection is preferably cooled.
- the temperature by which the first film is cooled is about 15 ° C. or more below the temperature at which the adhesive system is applied to the first film.
- a temperature difference of at least 20 ° and particularly preferably of at least 25 ° is preferably selected.
- a conventional laminating mill can be used to carry out the method according to the invention.
- the first film can be cooled by cooling the laminating roller itself, over which the film runs during the lamination with the second film.
- any other cooling device with the same effect can also be provided, such as a cooling channel through which the first film runs.
- the web speed of the films is typically selected in the range from 200 to 300 m / min., Preferably from 200 to 250 m / min., For the process according to the invention.
- the amount of adhesive system applied depends on the type of film to be laminated and the type of adhesive system itself.
- the application amount is usually between 1.5 to 4 g / m 2 , preferably 2.0 to 3.0 g / m 2 and in particular 2.5 to 2.7 g / m 2 .
- the web tension should be regulated so that a uniform tension is exerted both on the two individual films and on the laminated film composite. This measure increases the overall product quality. This also promotes the quality of the adhesive and the winding of the film.
- any solvent-free adhesive system can be used for the method according to the invention.
- These adhesive systems contain as an adhesive component a polyester resin with hydroxyl end groups, which is the reaction product of a linear aliphatic diol with 2 to 10 carbon atoms and a linear dicarboxylic acid.
- the polyester resin is crystalline at room temperature and has a melting point of about 80 ° C or less, with lower melting polyester resins being preferred.
- the number average molecular weight (M n ) is from about 300 to about 5,000 and the OH number is from about 20 to 350, with from about 100 to about 250 being preferred.
- aliphatic, preferably linear, or aromatic diisocyanate is used as the hardener component.
- aliphatic diisocyanates as can also be used in a suitable manner according to the invention, are polymeric hexamethylene diisocyanate and dicyclohexylmethane 4,4'-diisocyanate.
- aromatic diisocyanates are methylene diphenyl diisocyanate and toluene diisocyanate.
- polyester resins are the reaction products of C 3 -C 6 diols, in particular n-butanediol and n-hexanediol, with adipic acid, azelaic acid and sebacic acid, with adipic acid being preferred.
- aliphatic hardeners in particular can also advantageously be processed with the method according to the invention.
- the use of aliphatic hardeners can be particularly advantageous for composite films that are intended for the food sector due to their health and ecological safety.
- Adhesive layers obtained with aliphatic hardener components are also lightfast, that is to say in contrast to adhesive layers obtained with aromatic hardener components, they do not yellow under the influence of light such as daylight.
- composite films obtained by the process according to the invention with aliphatic hardeners are ready for further processing after a post-curing time of approximately three days.
- an aliphatic adhesive system is used for the present invention, which contains a polyester resin as adhesive component, which is sold by Rohm and Haas (formerly Morton) under the name Mor-Free VP 130-01, and polymeric hexamethylene as hardener components -Diisocyanate, which is marketed by Rohm and Haas under the name Mor-Free VP 200 C.
- the ratio of adhesive component to hardener component can vary depending on the type of film to be connected and is typically chosen according to the manufacturer's instructions.
- a suitable mixing ratio for the process according to the invention can be selected in a range from preferably 100: 55 to 100: 70 (adhesive: hardener).
- the proportion of hardener can be increased as required without impairing the barrier properties of the composite films obtained.
- aliphatic and aromatic diisocyanates can be used for the hardener component.
- the properties of the adhesive layer and thus of the composite film also depend on the type of the individual adhesive system components used, such as the hardener components used, certain properties of the composite film obtained can be modified as required by the use of such systems.
- aromatic hardener components can improve the barrier resistance of the composite film against moist gases.
- the proportion of aromatic monomers in the hardener component is in principle not subject to any restrictions, the proportion of aromatic monomers in the hardener component should be chosen such that no free aromatic diisocyanates are detectable in the adhesive layer obtained after the hardening time of the composite film. In other words, after the curing time, the total amount of aromatic hardeners should have reacted with the adhesive component.
- the proportion of free aromatic monomers is selected in a range of approximately 0.1%. It has been shown that with a proportion of approximately 0.1% of aromatic monomer, the aromatic monomer in the composite film obtained can no longer be detected after seven days.
- a suitable example of a hardener component which contains approximately 0.1% of aromatic diisocyanates are hardeners, such as those sold by Rohm and Haas under the names Mor-Free VP 413 A / S and Mor-Free VP 413 A. ,
- the method according to the invention is suitable for laminating any materials known per se for the production of composite films, such as plastic films, metallized plastic films with a thin metal coating, for example an aluminum coating, or also for laminating plastic films on paper.
- plastic films are films made of polyolefins such as polyethylene and polypropylene, polyesters such as polyethylene terephythalate, polyamide such as PA6 and co-extruded films.
- the number of foils that make up the composite foil is in principle not subject to any particular restriction.
- the composite film can therefore contain two, three, four or more films.
- Such films are also the subject of the invention.
- a barrier layer made of an adhesive system that the reaction product of a polyester resin with hydroxyl end groups as the adhesive component and an aliphatic or aromatic diisocyanant as the hardness component
- water vapor transmission rates of less than 1 g / (m 2 xd), and preferably of less than 1, 5 g / (m 2 xd) are obtained.
- Such composite films obtained according to the invention also show particularly low values for the oxygen permeability and nitrogen and carbon dioxide permeability.
- composite foils can be obtained from metallized plastic foils, the composite foils obtained being virtually impermeable to water vapor and the gases mentioned.
- a PVDC-coated polyester film as is commercially available, is preferably used, such as, for example, a PVDC-coated PET film with a thickness of 12 ⁇ m.
- FIG. 1 schematically shows a laminating device as can be used for the method according to the invention.
- the adhesive system components preheated to the application temperature are in a mixing tube 1, for example in the vortex process mixed and sprayed into a gap 9 between a pre-metering 2 and metering roller 3 and applied to the first film A via an application roller 4.
- the coating of the coated first film A with the second film B is preferably carried out immediately after the adhesive has been applied, in that the coated first film A is passed over a cooled laminating roller 5 for cooling and simultaneous laminating. As the coated first film A runs over the cooled laminating roller 5, the adhesive system applied to the first film A is subjected to immediate cooling, similar to a quenching.
- the cooling roller 5 is typically cooled to 15 ° C to 25 ° C.
- the device shown is additionally provided with pressure rollers (called impression roller) 6 and 7 and a supporting pressure roller (called impression roller) 8.
- impression roller pressure rollers
- impression roller a supporting pressure roller
- the pressure roller 6 is applied above the application roller 4 and the pressure roller 7 provides the necessary pressure for the incoming second foil B to be laminated onto the coated first foil.
- the laminated film composite leaves the laminating roller 5 in the direction of the arrow shown in FIG. 1 and reaches a winding (not shown in the figure).
- the composite film is preferably subjected to a second cooling again before winding.
- the composite film can be passed over a second cooling roller (not shown).
- This second chill roll is also typically cooled to 15 ° C to 25 ° C.
- the individual components of the adhesive system i.e. the adhesive component and the hardener component, are heated to the application temperature for a sufficiently long period of time before mixing and applying to the first film in order to achieve a homogeneous heating of the amount of adhesive and the amount of hardener.
- the individual components can be placed in heat containers.
- the individual components of the adhesive system are preferably kept under a protective gas atmosphere, such as a nitrogen atmosphere.
- the films to be laminated can be subjected to a corona treatment before laminating, in order to improve the wettability with adhesive, in order to achieve an improvement in the bond strength.
- Foil composites that have been subjected to a corona pretreatment tend to have electrostatic attraction effects. Corona pretreatment should therefore be avoided for applications in which such side effects can interfere.
- the tension that is exerted on the individual foils A and B and on the foil composite is to be coordinated with one another so that a uniform tension is exerted on the foils or the foil composite.
- the general product quality can be increased and tension-free film composites can be obtained.
- the winding of the film composite is also supported and a uniform winding is obtained.
- the foils were laminated using a Variocoater LF laminating machine manufactured by Windmöller & Hölscher (W&H).
- a polyester resin with hydroxyl end groups was used as the adhesive component
- Rohm and Haas is sold under the product name Mor-Free VP 200 C.
- the adhesive system components were preheated in heat containers under a nitrogen atmosphere to the application temperature of 60 ° C.
- the temperature control was carried out for an adhesive system quantity of 400 kg for 24 hours.
- the supply lines for the adhesive components to the metering gap 9 between the front metering roller 2 and metering roller 3 were made via heated supply systems.
- the application quantity was between approx. 2.6 to 3.0 g / m 2 and the production speed was 200 m / min.
- the temperature of the laminating roller was set at 20 ° to 25 ° C.
- a second chill roll was provided before winding, which also had a temperature of 20 ° to 25 ° C.
- a polyester resin was used as the adhesive component, which is sold by Rohm and Haas under the product name Mor-Free XVP PE 130-01.
- a hardener component with aromatic diisocyanate was used, as is also marketed by Rohm and Haas under the product name Mor-Free 413 A with a proportion of free toluene diisocyanate (TDI) of less than 0.1%.
- TDI free toluene diisocyanate
- Mor-Free VP 200C with hexamethylene-1, 6-diisocyanate from Rohm and Haas was used as the hardener component.
- the application rate for Examples 7 and 9 was between 2.8-2.9 g / m 2 or between 2.6-2.8 g / m 2 and for Example 8 between 2.5-2.6 g / m 2 ,
- PP means polypropylene, PE polyethylene, PA polyamide, PET polyethylene terephthalate, LDPE low density polyethylene, LLDPE linear low density PE, met.PP or met.PET metallized PP or metallized PET, C (reproduced) a co-extruded Foil with a second thin layer of polyethylene, U (prefixed) an unoriented foil and O (prefixed) an oriented foil, and X (repositioned) a coating with PVDC (polyvinyl dichloride).
- PVDC polyvinyl dichloride
- test conditions were:
- Determination of the oxygen permeability The determination was made according to DIN 53 380. The test conditions were
- the lower detection limit of the test method used is
- test conditions were:
- test conditions were:
- the lower detection limit of the test method used is
- OPP C 20 // white PE 30 to 100 PET 12 // met. OPP C 20
- OPP 20 // met.
- OPP 15 to 20 // PE 30 to 100 PET 12 // met.
- OPP 15 to 20 // PE 30 to 100 PET 12 // met.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Laminated Bodies (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP02757732A EP1383653A2 (de) | 2001-03-30 | 2002-03-29 | Verfahren zur herstellung von verbundfolien mit einem lösungsmittelfreien klebersystem |
AU2002308113A AU2002308113A1 (en) | 2001-03-30 | 2002-03-29 | Method for producing composite films by using a solvent-free adhesive system |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10116065.8 | 2001-03-30 | ||
DE10116065 | 2001-03-30 | ||
DE10153959 | 2001-11-06 | ||
DE10153959.2 | 2001-11-06 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2002079304A2 true WO2002079304A2 (de) | 2002-10-10 |
WO2002079304A3 WO2002079304A3 (de) | 2003-03-27 |
Family
ID=26008965
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2002/003558 WO2002079304A2 (de) | 2001-03-30 | 2002-03-29 | Verfahren zur herstellung von verbundfolien mit einem lösungsmittelfreien klebersystem |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP1383653A2 (de) |
AU (1) | AU2002308113A1 (de) |
DE (1) | DE10214006A1 (de) |
WO (1) | WO2002079304A2 (de) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1928754A4 (de) * | 2005-08-29 | 2009-11-25 | Exopack Technology Llc | Fettbeständiger falzbodenbeutel mit klebeverschluss, klebeverschluss für beutel und verwandte verfahren |
US9056697B2 (en) | 2008-12-15 | 2015-06-16 | Exopack, Llc | Multi-layered bags and methods of manufacturing the same |
CN108162559A (zh) * | 2017-12-20 | 2018-06-15 | 浙江科达包装机械厂 | 一种编织袋四辊复合装置 |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10258431B4 (de) * | 2002-12-13 | 2008-03-06 | National Starch & Chemical Gmbh & Co. Kg | Haus- oder Wohnungseingangstür |
DE102009003473A1 (de) * | 2009-02-12 | 2010-09-23 | Fsd Folienservice Deutschland Gmbh | Kaschierverfahren sowie Kaschiervorrichtung |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4496417A (en) * | 1982-11-12 | 1985-01-29 | Adolph Coors Company | Control stretch laminating device |
EP0906944A2 (de) * | 1997-09-17 | 1999-04-07 | Morton International, Inc. | Lösungsmittelfreier Laminierklebstoff mit Barrierewirkung |
EP1081170A2 (de) * | 1999-07-27 | 2001-03-07 | Takeda Chemical Industries, Ltd. | Gassperrpolyurethanharz |
-
2002
- 2002-03-29 EP EP02757732A patent/EP1383653A2/de not_active Withdrawn
- 2002-03-29 WO PCT/EP2002/003558 patent/WO2002079304A2/de not_active Application Discontinuation
- 2002-03-29 DE DE10214006A patent/DE10214006A1/de not_active Withdrawn
- 2002-03-29 AU AU2002308113A patent/AU2002308113A1/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4496417A (en) * | 1982-11-12 | 1985-01-29 | Adolph Coors Company | Control stretch laminating device |
EP0906944A2 (de) * | 1997-09-17 | 1999-04-07 | Morton International, Inc. | Lösungsmittelfreier Laminierklebstoff mit Barrierewirkung |
EP1081170A2 (de) * | 1999-07-27 | 2001-03-07 | Takeda Chemical Industries, Ltd. | Gassperrpolyurethanharz |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1928754A4 (de) * | 2005-08-29 | 2009-11-25 | Exopack Technology Llc | Fettbeständiger falzbodenbeutel mit klebeverschluss, klebeverschluss für beutel und verwandte verfahren |
US9056697B2 (en) | 2008-12-15 | 2015-06-16 | Exopack, Llc | Multi-layered bags and methods of manufacturing the same |
CN108162559A (zh) * | 2017-12-20 | 2018-06-15 | 浙江科达包装机械厂 | 一种编织袋四辊复合装置 |
Also Published As
Publication number | Publication date |
---|---|
WO2002079304A3 (de) | 2003-03-27 |
DE10214006A1 (de) | 2002-10-24 |
AU2002308113A1 (en) | 2002-10-15 |
EP1383653A2 (de) | 2004-01-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE69806709T2 (de) | Lösungsmittelfreier Laminierklebstoff mit Barrierewirkung | |
DE2907186C2 (de) | Verfahren zum Herstellen eines hochglänzenden Verbundmaterials | |
DE4143454C2 (de) | Verfahren zur Herstellung eines wasserdampfdurchlässigen Materials sowie ein solches Material | |
WO2009043777A2 (de) | Verfahren zur herstellung eines leichtblechs | |
DE69716891T2 (de) | Verfahren zur Herstellung von synthetischem Papier aus biaxialorientiertem Polypropylen mit hohem Glanz und der Fähigkeit schnell zu trocknen beim Bedrucken | |
WO2010108953A1 (de) | Extrusionsbeschichtetes band für starre verpackungen | |
DE1814910C2 (de) | Dielektrikum für Kondensatoren | |
DE2431984C3 (de) | Verfahren zur Herstellung von Schichtstoffen | |
EP0542160B1 (de) | Heisssiegelbeschichtung auf Dispersionsbasis | |
DE1810608C3 (de) | Druckempfindliches Übertragungselement und Verfahren zu seiner Herstellung | |
WO2002079304A2 (de) | Verfahren zur herstellung von verbundfolien mit einem lösungsmittelfreien klebersystem | |
DE2918923C2 (de) | Schichtstoff mit einer Polyvinylidenfluoridschicht | |
EP1824938B1 (de) | Primerlose verklebung von profilen | |
DE3307090A1 (de) | Verfahren zum herstellen eines schichtstoffes aus kohlenstoff | |
EP1517786B1 (de) | Mehrschichtmaterialien zum herstellen von verpackungen | |
EP1119455A1 (de) | Mit mehreren schichten beschichtete folien und deren verwendung im automobilbau | |
DE4121716C2 (de) | Schmelzkleber und dessen Verwendung | |
EP0283651B1 (de) | Verfahren zur Herstellung von Lackschichten und Lackfolien | |
DE1469467C3 (de) | ||
DE3110754A1 (de) | Verfahren zur herstellung eines mit durch elektronenstrahlen gehaertetem lack beschichtetem flaechenfoermigen traegermaterials mit matter oberflaeche | |
EP3323606B1 (de) | Trennverbund | |
DE2811151C3 (de) | Verfahren zum Herstellen von mehrschichtigen Verbundfolien | |
EP0795574B1 (de) | Folie mit einseitig rauher Siegelschicht und daraus hergestellte Verbundfolien | |
EP3098070B1 (de) | Verpackungselement | |
DE69316813T2 (de) | Epoxyharz Glasmatte und Verfahren und Vorrichtung zu ihrer Herstellung |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A2 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2002757732 Country of ref document: EP |
|
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
WWP | Wipo information: published in national office |
Ref document number: 2002757732 Country of ref document: EP |
|
NENP | Non-entry into the national phase |
Ref country code: JP |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: JP |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: 2002757732 Country of ref document: EP |