Patent Application
20160137869
1. Field of the Invention
The invention relates to plastic containers having a scratch and moisture resistant barrier coating against oxygen or carbon dioxide. Furthermore, the invention relates to a process for manufacturing of such containers.
2. Description of the Related Art
Plastic containers for food and beverages from polyethyleneterephthalate (PET), polypropylene (PP) or polyethylene (PE) are long known and are mostly produced in stretch blow molding processes.
It is also known to apply a barrier coating on such containers in order to reduce the permeation of gases, especially oxygen or carbon dioxide into or out of the container, thereby improving the shelf life of the packed goods.
For example, EP 2532600, EP 2431409, EP 2532600, WO 03/037969 Al, GB 879595, GB 2337470, WO 2004/089624, DE 10153210 and DE 10207592 Al describe the use of polyvinyl alcohol as gas barrier on PET bottles with an additional top coat comprising polyvinyl butyral to improve the water resistance of the barrier coating. Such multilayer coatings show a good barrier performance against oxygen and carbon dioxide, scratch resistance and are recyclable after mechanically destroying the top layer due the to the water solubility of the barrier coating.
The gas barrier disclosed in the prior art consists of or comprises polyvinylalcohol (PVA). PVA is a polymer obtained by hydrolysis of polyvinylacetate and contains vinylalcohol and vinylacetate subunits. Usually, PVA has a hydrolysation degree of 90-99 Mol %, which means that 1-10 Mol % vinylacetate subunits are still present in the polymer chain. Depending on the amount of vinylacetate subunits, PVA is more or less soluble in water. Therefore, coatings comprising PVA have a certain moisture sensitivity and can deteriorate under humid conditions, which has a negative impact on the overall gas barrier properties of the coating.
To improve the moisture sensitivity of gas barrier coating comprising PVA, JP 11349713 proposes a polyvinylalcohol/polyvinylacetal/ethylene terpolymer as gas barrier coating of PET substrates. The gas barrier coating according to JP 11349713 has a low adhesion to the PET surface, which makes the coating vulnerable to mechanical and moisture impact and does not provide sufficient adhesion on the substrate. Insufficient mechanical stability may lead to delamination during the expansion process of coated preforms.
An object of the invention was to improve the mechanical stability of a gas barrier coating on a PET surface, especially for subsequent stretch-blown processing of the PET surface. The present invention provides a process for producing a plastic container with a barrier coating comprising the steps a) applying at least one coating layer of a first polyvinyl acetal on at least a part of the plastic container; b) applying at least one coating layer of vinylalcohol/vinylacetate/ethylene terpolymer (PVAE) on the first polyvinyl acetal layer; c) applying at least one top coating layer of a second polyvinyl acetal on the PVAE layer.
Surprisingly is was found that although the gas barrier coating disclosed in JP 11349713 contains hydrophobic groups derived from ethylene, adhesion on polyvinylacetal is not impaired during stretching as compared to polyvinylalcohol. In addition, the moisture sensitivity is reduced, thereby improving the gas barrier features of the coating under humid conditions.
The first layer of polyvinyl acetal provided in step a) serves as base coating for the subsequent added barrier coating of polyvinyl alcohol and the second (top) layer of PVAE. The first base coating of polyvinyl acetal has strong adherence to the plastic material of the container and provides support for the PVAE layer provided in step b) and the top coating layer of polyvinyl acetal provided in step c).
Since PVAE adheres very well to polyvinyl acetal and vice versa, the subsequent added layers are likewise mechanically stable and result in a mechanically stable overall coating after the final shaping process of the container. PVAE reduces the gas permeability (especially O2 and CO2) of the substrate significantly, thereby improving the shelf-life of packed foods, soft drinks or beer.
The barrier coating comprising the layers manufactured in steps a, b and c) can be applied on at least a part of the outside or the inside of the containers. In another embodiment of the invention, the barrier coating may be applied to at least a part of the outside and inside of the plastic container or a preform thereof.
The term “at least a part of the outside or the inside of the container” refers to any part of the container where the gas barrier of the plastic material shall be improved by the method of the invention. In one variant of the invention, the entire outer or inner surface of the container is coated. In another variant, only the parts of the container are coated which have a lower gas barrier as compared to other parts. It is within the invention to coat only the lid of a container which, has on other parts, a sufficient low gas permeability. For example, containers of multilayer cardboard have a good gas barrier, but are closed with lids having a low gas barrier. To improve the overall gas barrier and the shelf life of the packed good, it is sufficient to provide the lid with a barrier coating of the present invention.
In the process according to the invention, the plastic container is optionally, prior to step a), pre-treated by chemical roughening, oxyfluorination, corona, electron beam or flame treatment.
The plastic material is optionally pre-treated or activated on the inside and/or outside.
Mechanical roughening can be achieved by a sandblast process, wherein the inside and/or outside surface of the container is provided with a roughness Rz of at least 100 μm, preferably 200 μm.
Preferably the pre-treatment or activation of at least a part of the surface of the plastic material results in an increase of the surface energy of the treated part of the plastic material of at least 25%, more preferably of at least 50%, based on the surface energy prior to treatment.
Untreated PET shows a surface energy of 30-45 mJ/m2. Accordingly, if the plastic material consists of PET, surface energy after pre-treatment should be at least 50 mJ/m2, preferably at least 55 mJ/m2 and especially at least 60 mJ/m2, the upper range being 150 mJ/m2.
Untreated PP has a surface energy of 25-35 mJ/m2. Accordingly, if the plastic material consists of PP, surface energy after pre-treatment should be at least 45 mJ/m2, preferably at least 50 mJ/m2 and especially at least 55 mJ/m2, the upper range being 150 mJ/m2. The surface energy is measured according the manual of Accu Dyne Testm Marker Pens.
Oxyfluorination is described in detail for example in WO2004/089624 or U.S. Pat. No. 5,900,321. The pre-treatment by oxyfluorination according to this invention may be conducted by exposing at least a part of the surface of the plastic material to a fluorine-containing gas mixture containing 0.01% to 5% by volume fluorine and optionally inert gases like nitrogen or air, or an additional reactive species such as chlorine or oxygen. Oxyfluorination for this invention may take place at a pressure of 10-10,000 kPa, preferably 100-5000 kPa, at a temperature of 10-90° C. with a time of exposure of 1 to 60 minutes.
Pre-treatment can enhance the adherence of the layers to the substrate. However, pre-treatment is an additional process step and the method of the invention provides in most cases mechanically stable coating layers which can be stretch-blown without cracks or delamination without pre-treatment. Accordingly, the present process can be performed in that the at least one coating layer of a first polyvinyl acetal is applied on the plastic container without pre-treatment.
Optionally after cleaning and pre-treatment, the first (base) layer of polyvinyl acetal is applied to the container.
For the first and second coating, polyvinyl acetal as the reaction product of polyvinyl alcohol with one or more aldehydes like formaldehyde, acetaldehyde, n-Butyraldehyde or iso-Butyraldehyde is used.
Suitable first and second polyvinyl acetals can be selected independently from the group consisting of polyvinyl(n)butyral, polyvinyl(iso)butyral, polyvinyl acetyl-co-(n)butyral, crosslinked polyvinyl(n)butyral, crosslinked polyvinyl(iso)butyral, Vinylalcohol/vinylacetate/ethylene terpolymer-(n)butyral, Vinylalcohol/vinylacetate/ethylene terpolymer-acetyl-co-(n)butyral.
The degree of acetalisation of the first and second polyvinyl acetals can be the same or different, but should be between 70 and 90 mol %, with the polyvinyl alcohol content being between 8 and 30 mol %.
Preferably, the first polyvinyl actetal has a viscosity of 10 to 70 m·Pas and/or second polyvinyl actetal has a viscosity of 50 to 500 m·Pas.
The viscosity of polyvinyl acetals are measured in a solution of 10% by weight in ethanol containing 5 weight % water at 20° C.
The polyvinyl acetal is applied on the surface of the container and/or the polyvinyl alcohol layer as a solution in an organic solvent, for example as a solution in methyl ethyl ketone (MEK), methanol, acetone or ethanol, for example by dip-coating, flowing or spraying. The concentration of the coating solution is preferably between 5 and 25% by Weight. The base layer of polyvinyl acetal thus applied may have a thickness of 0.01 to 5 μm.
Surplus coating material may be removed by spinning of the plastic material. The coating is dried at room temperature for 4-8 hours (or overnight), or at elevated temperature in an oven with temperatures between 30 and 60 ° C. for 0.5 to 2 hours. With the aid of appropriate machinery like conveyors with heaters, fast drying/curing is obtained in 15-30 sec.
After the first polyvinyl acetal layer is applied to at least a part of the container, the plastic material is coated with PVAE as a barrier coating on the first layer of polyvinyl acetal. Preferably, the PVAE has a degree of saponification/hydrolysis of 80 to 99 Mol %, preferably of 90 to 99 Mol %. The PVAE layer does not contain a plasticizer except some traces of moisture originating from the coating process.
The PVAE used in the present invention preferably has a content of ethylene groups of 1 to 20 mol %, more preferably between 3 and 10 Mol %. The degree of polymerisation is between 200 and 5000, preferably between 400 and 3000 or most preferably 700 and 1000.
Preferably, the PVAE has a viscosity of 10-100 m·Pas.
The viscosity of the PVAE is measured in a solution of 10% by weight in water at 20° C.
The coating layer from the PVAE may have a thickness of 0.01 to 5 μm. Preferably, the PVAE is applied as aqueous solution, for example by dip-coating, flowing or spraying. The concentration of the coating solution is preferably between 5 and 25% by weight.
Again, surplus coating material may be removed by spinning of the plastic material. The barrier-coated plastic material is dried to remove essentially all water, at an ambient temperature of 10 to 90° C., preferably 10-50 ° C., optionally at reduced pressure, and then subjected to the protective top-coating with the second polyvinyl acetal.
First and second polyvinyl acetals may be different or identical polymers. The process of coating and drying of the first and second layer of polyvinyl acetal may be different or identical. In order to reduce the complexity of the process it is preferred to utilize identical polyvinyl acetals and methods for both steps a) and c).
The barrier coating of steps a, b) and c) can be applied on at least a part of the outside or the inside of the plastic container. It is furthermore possible to apply the barrier coating of steps a, b) and c) on at least a part of the inside and at least a part of the outside of the plastic container.
It is possible to incorporate dyes or pigments in the barrier coating, the base coating, and/or the protective top coating. Suitable pigments are for example SiO2, Al2O3, or TiO2. As dyes, “Rhenol”-type dyes from Clariant can be used. The concentration of dyes or pigments in each layer can range from 0.01 to 5 weight %, based on the polymer.
Subsequent to coating and drying according to the steps a, b, and c, the plastic material may be shaped into a container by a blow-forming process, a blowing process like stretch blowing, or injection stretch blow moulding. The optional step d) may be performed prior to or after the blowing process.
The plastic material to be coated with the process of the invention may comprise or consist of polymers selected from the group PET, PP, PE (polyethylene) and COC (cyclic olefin copolymer.
The plastic material may have any two or three dimensional shape, like film, or a container, or a part of a container. The coating may also be applied on a first shaped body (preform) which is then formed into the container. “Preform” as used in this application is not limited to any particular shaped body, especially not to preforms of a bottle, and may characterize any first shaped body which is used to produce the final container by another shaping process.
Yet another object of the invention is a process to manufacture a container by subjecting an optionally pre-treated preform of the container to a process comprising the already described coating steps a, b and c, and subsequently shaping the preform into the final shape of the container. Preferably, shaping the preform is performed by a blowing process like stretch blowing or injection stretch blow moulding.
A stretch blow process for the invention is shown by way of example in
The coating according to the invention may be applied to the outside or the inside or both sides of the container.
The containers coated by the process of the invention may be used, inter alia, for food, beverages, drugs, spices, coffee, tea or chemicals. The container may have a shape of capsules, blister packages, sachets, envelopes, jerry cans, bottles, jars and lids thereof.
The advantage of the process according to the invention is that the coating is flexible enough to survive a stretch blow process, yet mechanically and chemically stable enough to protect packed goods.
A PET sheet was coated without pre-treatment with layers as shown in table 1. Then, the moisture resistance was analysed by first conditioning in a climate chamber (23° C./98% r.h.) and weighing after 1, 3, 5 and 10 days using an analytical balance to obtain the absorbed moisture. The value for the absorbed moisture content was determined by calculation of the mass difference before and after conditioning in the climate chamber. The determined difference was calculated as percentage.
Table 1 shows the measured value for the layer system A/B/A according to the invention and a layer system C/D according to the prior art.
The layer system corresponding to the invention as described herein shows a 10% lower gas transmission rate after 10 days of conditioning due to better moisture protection of the barrier layer that the prior art.
A: polyvinyl butyral type Mowital B 30 HH (Kuraray Europe GmbH)
B: Vinylalcohol/vinylacetate/ethylene terpolymer type Exceval AQ4104 (Kuraray Europe GmbH)
C: polyvinyl accohol type Mowiol 28-99 (Kuraray Europe GmbH)
D: polyvinyl butyral type Mowital B30 HH (Kuraray Europe GmbH)
Mowital B30 HH (Kuraray Europe GmbH) has a viscosity of 35-60 m·Pas.
Exceval AQ4104 has a viscosity of 3.8-4.5 m·Pas, an ethylene content of less than 10 Mol % and a degree of hydrolysis of 98-99%
Adhesion Test
In order to show that barrier layers consisting of PVAE have a significantly better adhesion to polyvinyl acetal layer 1 and 3, an adhesion test was performed as a peel-off test using flat test bodies (foils).
A polyvinyl acetal film as layer 1 was coated with a PVAE or PVA layer by bar coating as known to one skilled in the art. This test body was then treated with a lamination adhesive and laminated on a lamination film (polyethylene). After drying and conditioning in a standard climate (23° C., 50 r.h.) the test body was cut into at least 7 strips. The strips were then peeled off using a tensile testing machine and the force measured which is necessary to peel off the PVAE layer from the polyvinyl acetal layer. The best and the worse of the 7 measured values were not accepted and the average value was calculated from the other five single values. The higher the values for the peel-off forces the better is the adhesion of the barrier layer to the polyvinyl acetal layer.
Exceval AQ4104 has a viscosity of 3.8-4.5 m·Pas, an ethylene content of less than 10 Mol % and a degree of hydrolysis of 98-99%.
Exceval HR 3010 has a viscosity of 12-16 m·Pas, an ethylene content of less than 10 Mol % and a degree of hydrolysis of 99-99.4%.
Mowiol 28-99 is a standard polyvinyl alcohol with a viscosity of 28 m·Pas and a degree of hydrolysis of >99%.
All materials are available from Kuraray Europe GmbH
Mechanical Stability
A test body of layers polyvinyl acetal (A), PVA or PVAE (B) and polyvinyl acetal (A) was prepared as disclosed in Example 1. Such laminates were subjected to a simple stretch test wherein the maximum factor of stretching, i.e. the ratio of the original size to the size of a test body before observing cracks or failures in the coating layer was determined.
As can be seen from table 2, layers of PVAE have significantly better adhesion to polyvinyl acetal than PVA. Table 3 shows that the system PVB/PVAE/PVB according to the invention shows a significantly better elongation behaviour as compared to the system PVB/PVA/PVB known from the prior art.
These tests show that plastic preforms coated with polyvinyl acetal/PVAE/polyvinyl acetal can be stretch-blown to a plastic container with less delamination than preforms coated with polyvinyl acetal/PVA/polyvinyl acetal.
Since coatings consisting of polyvinyl acetal/PVAE/polyvinyl acetal have a better elongation behaviour, the blown containers will have a barrier coating with less cracks or failures than blown containers coated with polyvinyl acetal/PVA/polyvinyl acetal.
| Number | Date | Country | Kind |
|---|---|---|---|
| 13176399.7 | Jul 2013 | EP | regional |
This application is the U.S. National Phase of PCT Appln. No. PCT/EP2014/064659 filed Jul. 8, 2014, which claims priority to European Application No. 13176399.7 filed Jul. 12, 2013, the disclosures of which are incorporated in their entirety by reference herein.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2014/064659 | 7/8/2014 | WO | 00 |
