Patent Application
20160002424
The present invention is concerned with the surface treatment of substrates, particularly filmic substrates, to improve their printability without adversely affecting their suitability for regulatory food contact approval.
Regulatory requirements for food contact approval in connection with packaging and labelling materials are becoming progressively more stringent. The presence of migratory additives in such materials can prevent their suitability for such approval when their intended use involves food contact as in, for example, packaging films and materials for grocery products. Increasingly, such considerations are also becoming relevant in labelling since it has become recognised that even non-food labelled products, such as toiletries and detergents for example, may come into contact with food products or their packaging in shopping baskets, delivery vehicles, warehouses, supermarket shelves and so on. As a consequence, regulatory requirements for labels seem likely to become more stringent, particularly with regard to the perceived unsuitability of migratory additives in food contact situations.
Labels, and also many packaging materials, are frequently required to carry print. Unfortunately, from the point of view of food contact approval, this requirement often necessitates surface modification of the label or packaging material to improve its printability. In the case of labelling films and packaging films, for example, such modification may involve the application of a surface coating—a printable coating—which adheres to the packaging or labelling substrate and provides a receptive surface for printing inks. However, such surface coatings frequently contain migratory additives such as slip and antiblock agents, antifogs, antistats, and processing aids. They may also contain other non-migratory but nevertheless undesirable (from a food contact approval point of view) materials such as crosslinkers and acid functional materials.
Consequently, there is a pressing need to provide printable films for packaging or labelling which are suitable for regulatory food contact approval.
Modified atmosphere dielectric barrier discharge (MADBD) treatment has been used for many years for the surface treatment of polymeric substrates. U.S. Pat. No. 7,147,758 for example is concerned with such treatments in the presence of a carrier gas, a reducing gas and an oxidising gas. It is not uncommon in the art for MADBD treatment to be called plasma treatment. In this specification no distinction is made between plasma treatment on the one hand and MADBD treatment on the other. However, both are treatments which typically take place in a modified gas atmosphere (i.e. an atmosphere other than air). Corona discharge treatment (also known as corona treatment or D treatment), is another form of dielectric barrier discharge which typically takes place at lower power (and with a larger electrode gap) than MADBD or plasma treatment, and typically takes place in an unmodified atmosphere—i.e. air.
Corona discharge treatment has been used considerably longer than MADBD treatment in the processing of polymeric films, and is an established technique in the industry. However, typically the manufacturers of modified atmosphere MADBD treaters have cautioned against using corona treatment in combination with MADBD treatment, apparently believing that the surface chemistry of MADBD treated film would be adversely affected by corona treatment. Consequently, it has rarely been contemplated to subject film to both MADBD and corona discharge treatment. U.S. Pat. No. 5,147,678 appears to contemplate such combinative treatments, but only in the context of laboratory experimentation and with unproven commercial utility. U.S. Pat. No. 7,824,600 expressly contemplates a two stage treatment in which a monoaxially oriented film is subjected to a plasma treatment before being laterally stretched and corona treated prior to winding onto a reel. This document fails to appreciate that any benefit may be derived from a further or alternative downstream treatment of the film, and instead concentrates only on multiple treatments taking place before winding of the film onto a reel. On the other hand the benefit of downstream treatment is apparently recognised in U.S. Pat. No. 7,410,675, but only in the context of a repetition of a treatment having already once been conducted on the film.
One problem with MADBD treatment is that whatever surface modification of the film takes place under such treatment, the effect is not permanent, so that a treated film with surface characteristics making it suitable for printing tends to lose those characteristics over time and revert to being unprintable or poorly printable. This causes serious problems in the film industry because film manufacturers are rarely responsible for printing the films they make. Commonly, film manufacturers will instead wind film onto a reel and ship it to their customers, typically printers or converters, who will unwind the film prior to converting and/or printing it. Inevitably in connection with a MADBD treated film, by the time the film is then printed much of the surface characterisation caused by the MADBD treatment has been lost. Hitherto, film manufacturers have consequently sought to guarantee the long-term printability of the film by means other than MADBD treatment—the provision of printable coatings on the film for example—with consequent disadvantages in the regulatory environment as far as food contact approval is concerned.
What was realised in our co-pending application PCT/GB2012/052396 is that the surface characterisation of the film caused by MADBD treatment can be revived, improved or reconstituted considerably after (even many months after) initial manufacture and MADBD treatment of the film by the apparently straightforward expedient of corona treating the previously MADBD treated film. The combination of an initial MADBD treatment (normally during manufacture of the film) and a downstream corona treatment to refresh or even augment the surface properties of the MADBD-treated film was not hitherto recognised in the art. Other combinatory and/or repetitious treatments mentioned in the art which also fail to appreciate this concept are disclosed in EP0947544, U.S. Pat. No. 7,300,859, U.S. Pat. No. 7,067,405, WO2008102408 U.S. Pat. No. 4,929,319, EP1620262, JP11256338 and JP9314773.
According to the present invention there is provided a process for producing a food contact approvable, printable film comprising:
a. providing a web of film having a width of at least about 1 cm and/or a length of at least 1 m and/or a weight of at least about 1 g and having a food-contactable surface;
b. at a first location subjecting at least a first surface of the film web to a modified atmosphere dielectric barrier discharge (MADBD) treatment;
c. winding the film web onto a reel;
d. transporting the wound film web to a second location;
e. unwinding the film web from the reel; and
f. subjecting the first surface of the film to corona treatment.
The film web may:
The film may comprise one or more migratory additives or substances in amounts such that not more than 75 mg, or not more than 50 mg, or not more than 25 mg, or not more than 10 mg of any such migratory additive(s) or substance(s) per dm2 of the food-contactable surface is or are able to migrate to the food-contactable surface of the film.
Preferably the film comprises either no migratory additives or substances, or one or more migratory additives or substances in amounts less than about 1 wt %, or less than about 0.5 wt %, or less than about 0.25 wt %, or less than about 0.1 wt %, or less than about 0.05 wt %, or less than about 0.025 wt %, or less than about 0.01 wt %.
Preferably, or optionally the width of the film web is at least about 2 cm; or at least about 5 cm; or at least about 10 cm; or at least about 25 cm; or at least about 50 cm; or at least about 1 m; or from about 1 cm to about 25 m; or from about 2 cm to about 20 m; or from about 5 cm to about 17.5 m; or from about 10 cm to about 15 m; or from about 25 cm to about 12.5 m; or from about 50 cm to about 12 m; or from about 1 m to about 10 m.
Preferably, or optionally the length of the film web is at least about 2 m; or at least about 5 m; or at least about 10 m; or at least about 25 m; or at least about 50 m; or at least about 100 m; or from about 2 m to about 50 km; or from about 5 m to about 40 km; or from about 10 m to about 30 km.
Preferably, or optionally the weight of the film web is: at least about 5 g; or at least about 10 g; or at least about 50 g; or at least about 100 g; or at least about 1 kg; or at least about 10 kg; or from about 1 g to about 10,000 kg; or from about 5 g to about 5,000 kg; or from about 10 g to about 2,500 kg; or from about 50 g to about 2,000 kg; or from about 100 g to about 1,500 kg; or from about 1 kg to about 1,250 kg; or from about 10 kg to about 1,000 kg.
In this specification we use the term MADBD treatment to refer to a treatment which takes place in a modified atmosphere (i.e. not air). Corona treatment is a treatment that takes place at a lower power, with wider electrode gaps than in MADBD treatment, and in atmosphere (i.e. air). MADBD and corona treatment are, respectively, terms of art which will be understood by skilled addressees such as film manufacturers or the operators of printing, laminating and coating machines.
The invention also provides a process in accordance with the foregoing, wherein the corona treated film obtained at step f) is printed shortly after the said corona treatment. By “shortly after” we mean preferably within 10 days, more preferably within 5 days and most preferably within 1 day. Often printing will take place within hours, if not minutes, or even seconds, of the corona treatment step.
Printing of the film may be by any known process, UV Flexo, screen or combination printing, as well as gravure, reverse gravure, for example. Preferably, the film is printed using one or more inks which is or are approved or approvable for food contact use.
The film may be subjected to the printing step before or after a sheet of the film has been severed from the web.
Optionally, the film may be subjected to other conversion steps—lamination, the provision of an adhesive layer and/or a release liner on the film web, before or after printing of the film and before or after severance of a sheet of film from the film web.
It is contemplated that the film may be subjected to MADBD treatment, and subsequently to corona treatment, only on its first surface or, optionally, on both surfaces. When both surfaces of the film are treated, it is sufficient for the purposes of this invention that only one surface be subjected both to MADBD treatment and, subsequently, to corona treatment. The other surface may be subjected to the same or similar treatment to the first surface, or to different treatment; for example only to MADBD treatment or only to corona treatment.
We have found that there are two primary factors in connection with the properties of the film at its first surface which determine its printability. These are the surface chemistry of the film on the one hand and its surface energy on the other. Surface chemistry is determinative of the ability of the film to bind with an ink applied to the surface, whereas surface energy is determinative of the wetting characteristics of an ink applied to the surface. Both good adhesion and good wettability are considered necessary to achieve a good printable film.
The surface energy of the film at its first surface is initially increased by the MADBD treatment. Preferably the surface energy of the film at its first surface immediately after MADBD treatment is at least about 46 dynes/cm, preferably at least about 50 dynes/cm, more preferably at least about 56 dynes/cm and most preferably at least about 60 dynes/cm.
Preferably the surface energy of the film at its first surface immediately after MADBD treatment is at least about 8 dynes/cm, preferably at least about 15 dynes/cm, more preferably at least about 20 dynes/cm and most preferably at least about 24 dynes/cm higher than the surface energy of the film at its first surface immediately before such MADBD treatment.
After MADBD treatment the surface energy of the film decreases over time. Generally, by the time the film web is subjected to corona treatment in accordance with the process of the invention, the surface energy has reduced from its high point immediately after MADBD treatment by at least about 10%, often at least about 15%, or even by as much as 20% or 25%. Preferably, the surface energy of the film immediately after the corona treatment is back to within at least 15%, or at least 10%, of its value immediately after MADBD treatment. In some cases the surface energy of the film immediately after corona discharge treatment may even be above its surface energy immediately after MADBD treatment.
The surface chemistry of the film is also affected by the MADBD treatment. Clearly, the affected characteristics will depend not only upon the nature of the film surface but on other factors such as the nature of the modified atmosphere, the energy level of the MADBD treatment, the size of the electrode gap and the duration of the treatment. For the purposes of this invention it is sufficient to state that the surface of the film following MADBD treatment will comprise a number of polar chemical species not present on the film surface prior to MADBD treatment. What we have now discovered is that subsequent corona treatment effects further changes to the surface chemistry of the film.
We have found that we are able to characterise surface chemistry of the film in terms of its functionality—that is to say, in particular the number of polar chemical species present at the surface of the film. Typically, the relative atomic concentration of polar chemical species measurable at the film surface immediately following MADBD treatment and subsequent exposure of the treated film to the atmosphere (whereupon any charged chemical species present on the film surface as a result of the MADBD treatment will be neutralized by the atmosphere) is y %, wherein y is a positive number. Because the effect of MADBD treatment dissipates over time as far as surface functionality is concerned, we generally find that the relative atomic concentration of polar chemical species measurable at the film surface immediately prior to the corona treatment step (after a period of time, generally of a least a few days, but often much longer, has elapsed after the initial MADBD treatment) is y−x %, wherein x is a positive number. Furthermore, because of the restorative or augmentative effect of the corona discharge treatment as concerns the functionality of the film, we then find that the relative atomic concentration of polar chemical species measurable at the film surface immediately after the corona treatment of step f) is y−x+z %, wherein z is a positive number.
Prior to MADBD treatment the surface of the film may, or may not, contain polar chemical species at its surface in any significant or substantial amount (above 1% relative atomic concentration for example). A polyolefin film for example essentially comprises only carbon-carbon and carbon-hydrogen bonds and is therefore substantially non-polar. On the other hand, a polyester film or an acrylic-coated film for example will already contain polar chemical species, including of course at its surface. In the process of the present invention the relative atomic concentration of polar chemical species measurable at the film surface immediately prior to MADBD treatment is q %, wherein q is zero or a positive number and wherein q is less than y. Preferably y−x+z is at least about 5, preferably at least about 10 greater than q.
In the process of the present invention, y−x+z is preferably at least about 10, more preferably at least about 10.5, still more preferably at least about 11, and most preferably at least about 11.5, or even at least about 12.
The precise nature of the chemical functionality engendered at the surface of the film by MADBD treatment and/or by subsequent corona treatment will depend upon many factors, including the chemical characteristics of the film itself at its surface (meaning or including where applicable the chemical composition of any skin layer or coating or lamination thereon), the nature of the modified atmosphere provided during the MADBD treatment, the power and duration of the MADBD treatment and/or the subsequent corona treatment and other ancillary parameters such as the environment, both physical and chemical, in which the film is treated and/or maintained. Generally speaking, in connection with polymeric films, examples of polar species extant at the surface of the film after or during such treatments will at least include fragments containing carbon-oxygen bonds. Such fragments may derive from the film itself and/or from the atmosphere in which the film is treated. Other polar fragments may derive from the modified atmosphere of the MADBD treatment, alone or in combination with materials from the film. For example, when the modified atmosphere of the MADBD treatment comprises nitrogen gas, there will likely be polar fragments comprising carbon-nitrogen bonds at the film surface after MADBD treatment. (However, with some films—polyurethane for example—the presence of carbon-nitrogen polar fragments at the film surface may not require the use of nitrogen gas in the modified atmosphere of the MADBD treatment.)
Generally the polar chemical species at the film surface after MADBD treatment will comprise one or more of the species selected from: nitrile; amine; amide; hydroxy; ester; carbonyl; carboxyl; ether and oxirane.
The technique of ToF-SIMS spectroscopy has been found to be a satisfactory method for measuring in qualitative terms the surface functionality (in terms of the identities of polar species present at the surface) of the film. However, for quantitative characterization (in terms of relative atomic concentration of polar species at the film surface) we have found the technique of XPS spectroscopy to be more useful. Other determinative methods will be apparent to the skilled addressee.
The modified atmosphere of the MADBD treatment will generally contain an inert carrier gas such as a noble gas or nitrogen, and at least one functional or reducing fluid such as acetylene, ethylene, hydrogen or silane for example. Oxidising fluids such as oxygen, ozone, carbon dioxide, carbon monoxide, nitric and nitrous oxides and, sulfur oxide, dioxide or trioxide may also be used.
Suitable film webs which can be used in this invention include webs formed from polymeric films. Polymeric film webs according to the invention can be made by any process known in the art, and the term includes, but is not limited to, cast sheet, cast film, or blown film. The film web may comprise a polyolefin film, for example polyethylene, polypropylene, polybutylene mixtures, blends and copolymers (both block and random) thereof, and/or other known polyolefins.
Alternatively, the film web may comprise a polyester film, a polyamide film, a polyurethane film, a polyvinylhalide film, acetate film or a biopolymer film such as a cellulosic film, a PLA film, a starch based film or a PHA film.
For printable film intended for use as labels or in other types of packaging, polyolefin films are preferred, especially oriented polypropylene films, and still more preferred is an oriented polypropylene film according to EP-A-0202812. The film may have additional layers around the core layer, for example comprising copolymers of ethylene and propylene or terpolymers of propylene, ethylene and butylene. The film may comprise a biaxially orientated polypropylene (BOPP) film, which may be prepared as a balanced film using substantially equal machine direction and transverse direction stretch ratios, or can be unbalanced, where the film is significantly more orientated in one direction (MD or TD). Sequential stretching can be used, in which heated rollers effect stretching of the film in the machine direction and a stenter oven is thereafter used to effect stretching in the transverse direction. Alternatively, simultaneous stretching, for example, using the so-called bubble process, or simultaneous draw stenter stretching may be used.
By “printable” is preferably meant “ink printable” and that in a standard ink pull-off tape test, scratch test, or UV flexo test conducted on a film according to the invention which has been printed on its first surface with a compatible ink and then cured (for example UV cured) and allowed to age for 24 hrs before testing, less than 50%, preferably less than 40%, more preferably less than 30%, still more preferably less than 20% and most preferably less than 10% of the ink is removed from the printed surface in the test. In a particularly preferred embodiment of the invention, less than 5%, or even as low as substantially 0%, of the ink is removed in such testing.
Also by “ink printable” is generally meant that in a standard ink pull-off tape test, scratch test, or UV flexo test conducted on a film according to the invention which has been printed on its first surface with a compatible ink and then tested immediately thereafter, less than 75%, preferably less than 60%, more preferably less than 50%, still more preferably less than 40% and most preferably less than 30% of the ink is removed from the printed surface in the test. In a particularly preferred embodiment of the invention, less than 20%, or even below 10%, of the ink is removed in such testing.
Also provided in accordance with the present invention is a printable film obtained or obtainable by the process of the invention. The invention also concerns a polymer labelstock film in accordance with the above printed on its first surface with at least one ink.
The invention also provides a process for ink printing comprising providing a film in accordance with the above and supplying to the first surface of the film by means of screen, flexo, inkjet or other printing means, at least one compatible ink.
The film, or any of its layers in the case of a multi-layer film, may comprise additional materials such as anti-block additives, opacifiers, fillers, UV absorbers, cross-linkers, colourants, anti-static agents, antioxidants, cavitating agents, slip additives and the like, subject to the aforementioned stipulations concerning the presence (if any) of migratory additive(s) or substance(s) within the film.
The films used in accordance with the present invention can be of a variety of thicknesses according to the application requirements. For example they can be from about 8 μm to about 240 μm, from about 8 μm or 20 μm to about 200 μm, from about 8 μm or about 20 μm or about 25 μm to about 150 μm, or from 8 μm or 20 μm or 25 μm to about 75 μm or about 100 μm or about 125 μm thick.
Preferably, the first location and the second location are remote from one another. More preferably the first location is a first factory or manufacturing site and the second location is a second factory or manufacturing site. The process of the invention allows a film manufacturer to operates steps a) and b) of the process to produce a printable film, which film can then be wound onto a reel and shipped to a customer (steps c) and d) of the process), such as a printer or converter, who will then operate steps e) and f) of the process and thereby refresh the film's printability performance following the diminishment in that performance that takes place during steps c), d) and e) of the process.
The invention also provides food-contact approvable or food-contact approved, printable or printed webs of film obtainable or obtained by the above described methods.
Consequently, according to the present invention there is provided a printable, food contact-approvable web of film having a width of at least about 1 cm and/or a length of at least 1 m and/or a weight of at least about 1 g and having a food-contactable surface, the film web comprising a substrate, and at least one polar functional group present at a food-contactable surface, and/or at an opposed surface, of the film and available to bond with an ink, the relative atomic concentration of the at least one polar functional group at the food-contactable and/or opposite surface of the film being at least about 1% and the concentration of the at least one polar functional group at the food-contactable and/or the opposed surface of the film being at least about 1% higher than the concentration of any of the same functional group present in the film immediately below the food-contactable and/or opposed surface, the film:
i comprising no migratory additives or substances; or
ii. comprising one or more migratory additives or substances in amounts such that not more than 10 mg of any such migratory additive(s) or substance(s) per dm2 of the food-contactable surface is or are able to migrate to the food-contactable surface,
with the proviso that when the film comprises no migratory additives or substances then the film is not a 55 μm thick biaxially oriented polymeric film having a core layer of random polypropylene/polyethylene copolymer and coextruded skin layers of polypropylene/polyethylene/polybutylene terpolymer constituting less than 1 μm of the 55 μm thickness, wherein the film:
i. is an uncoated film; and/or
ii. is a principally or entirely polyolefinic film; and/or
iii. is substantially free from acrylic components; and/or
iv. is substantially free from acrylate components; and/or
v. is substantially free from cross-linkers; and/or
vi. is substantially free from polyurethanes; and/or
vii. is substantially free from polyesters; and/or
viii. is substantially free from plasticisers; and/or
ix. is substantially free from reactive components; and/or
x. is substantially free from strong electrophiles; and/or
xi. is substantially free from any material in any amount which would cause the film to fail extraction tests according to the protocol described in the US Code of Federal Regulations, Title 21 Food and Drugs, Chapter I—Food and Drug Administration, Department of Health and Human Services, Part 177, Section 1520 Olefin Polymers (Edition: Apr. 1, 2012); and/or
xii. is substantially free from any material in any amount which would cause the film to fail migration tests with food-simulating liquids using the test methods described in European Standard EN 1186:2002 (Parts 1-15).
By “substantially free” is meant preferably <0.5 wt %, more preferably <0.25 wt %, even more preferably <0.1 wt % and most preferably 0-0.05 wt % or 0 wt %.
By “immediately below” is preferably meant about 0.5 μm below; or about 1 μm below; or about 2 μm below. Preferably, the concentration of the at least one functional group at the food-contactable surface of the film is at least about 2% higher, more preferably at least about 5% higher and most preferably at least about 10% higher than the concentration of any of the same functional group present in the film immediately below the food-contactable surface. For the avoidance of doubt, there need not be any of the at least one functional group present in the film immediately below its food-contactable surface; although there may be.
The film may be substantially free from cross-linkers, examples of which include acrylate-functional cross-linkers, aziridine cross-linkers and ionomeric cross-linkers for example polyacid cross-linkers and multi-valent metal-containing cross-linkers.
The film may be substantially free from reactive components, examples of which include ethylenically unsaturated compounds and imines.
The at least one polar functional group may be a nitrogen-containing functional group, for example a nitrile, amine or amide group; an oxygen-containing group for example a hydroxy, ester, carbonyl, carboxyl, ether, oxirane or silica group; a halogen-containing group wherein the halogen is fluorine or chlorine for example; and/or a sulphur-containing group for example a thiol group.
Preferably the at least one polar functional group is a nitrogen-containing functional group.
Additionally, at least one non-polar functional group may be present at the food-contactable surface and/or at an opposed surface of the film and be available to bond with an ink. In particular, the non-polar functional group may be an ethylenic group.
The substrate may comprise a monolayer or it may comprise multiple layers, one or more of which constitutes a core layer of the film. Preferably at least one component of the monolayer or the core layer is not a random polypropylene/polyethylene copolymer. Random polypropylene/polyethylene copolymer may be present in the monolayer, or the core layer as the case may be, but is preferably not the sole component of the layer.
Preferably, the ink is a food-contact approvable or food-contact approved ink.
Also provided in accordance with the invention is a printed, food contact-approvable film comprising a substrate and an ink bound to the substrate by means of at least one carbon-nitrogen bond.
Also provided in accordance with the invention is a printed, food contact-approved film comprising a substrate and an ink bound to the substrate by means of at least one carbon-nitrogen bond.
The invention depends upon the functionalisation of the film at its surface to generate a film which is preferably:
a. a polyolefinic film comprising substantially no non-polyolefinic polymeric constituents;
b. substantially free from cross-linkers at its food-contactable surface; and/or
c. substantially free from acrylic and/or acrylate materials at its food-contactable surface; and/or
d. substantially free from polyurethanes, polyesters, plasticisers, reactive components and/or strong electrophiles at its food-contactable surface.
Also provided in accordance with the invention is a sheet of film severed or otherwise separated from such a web.
The invention also provides a label or package comprising a sheet of film in accordance with the invention.
Also provided is an article labelled or packaged by a label or package in accordance with the invention.
Also provided in accordance with the invention is the use of a sheet of film according to the invention in a labelling or packaging application in which it is necessary for the film to be food-contact approvable or food-contact approved.
Consequently, the invention provides a printed polymeric film sheet having a width of at least 1 cm and a length of at least 1 cm and comprising at least one ink bound to the surface of the film sheet via a functional group present at the surface of the sheet at a relative atomic concentration of a % but present at a location immediately below the surface of the sheet in an amount of from 0 to b %; b being less than a.
a may for example be at least about 1% or at least about, 2% or at least about, 3% or at least about, 4% or at least about 5%. b may for example be at least about 10%, at least about 20%, at least about 30%, at least about 40%, or at least about 50% lower than a.
By “immediately below” is preferably meant about 0.5 μm below; or about 1 below; or about 2 μm below.
The invention further provides a printable polymeric film web having a width of at least about 1 cm and/or a length of at least 1 m and/or a weight of at least about 1 g and having a food-contactable surface and comprising functional groups at the food-contactable surface capable of binding to an ink, the functional groups comprising a combination of functional groups inducible on the film surface by means of MADBD treatment and of functional groups inducible on the film surface by corona treatment.
The functional groups may comprise a combination of functional groups inducible on the film surface by means of sequential treatment of the film by MADBD treatment and subsequently by corona treatment.
Preferably, the subsequent corona treatment is carried out at least 1 week, at least 2 weeks, at least 1 month or at least 3 months after the MADBD treatment.
The invention will now be more particularly described with reference to the following Examples.
A biaxially oriented polymeric film having a core layer of random polypropylene/polyethylene copolymer and coextruded skin layers of polypropylene/polyethylene/polybutylene terpolymer was manufactured by means of a bubble process in the form of a web having a width of 2.9 m and a length of 8,000 m. The film has a total thickness of 55 μm, with the skin layers between them constituting less than 1 μm of that thickness.
Examples 1 to 6 below all used severed sheets from this film as a starting material.
Corona treatment of the film involved an electrical process using ionized air to increase the surface tension of non-porous substrates. Corona treatment converts the substrate surface from a normally non-polar state to a polar state. Oxygen molecules from the corona discharge area are then free to bond to the ends of the molecules in the substrate being treated, resulting in an increase in surface tension. Generally a film to be treated would pass under a filament where a streaming discharge though the air would earth on the film at speeds appropriate for a printing process.
MADBD treatment of the film differs from corona treatment in that the rate at which electron bombardment occurs is up to 100 times greater. This increased cross-linking activity forces a greater ion bombardment onto the substrate surface. This result increases etching of the substrate's surface, and stronger bonding attributes across the length of the film. In addition to these surface reactions, plasma also facilitates the use of chemical gases which can produce controlled chemical reactions on the surface as well. Generally a film to be treated would pass under a series of solid electrodes where a glow discharge though the modified atmosphere would earth on the film at speeds appropriate for a coating process.
The following film samples were used:
Example 1: untreated film (control; comparative).
Example 2: film treated with MADBD at 50 w/cm2 in an atmosphere of N2 and acetylene; 100 ppm acetylene.
Example 3: film treated with MADBD at 55 w/cm2 in an atmosphere of N2 and acetylene; 75 ppm acetylene.
Example 4: film treated with MADBD at 45 w/cm2 in an atmosphere of N2 and acetylene; 100 ppm acetylene.
Example 5: film treated with MADBD at 75 w/cm2 in an atmosphere of N2 and acetylene; 100 ppm acetylene.
Example 6: film treated with MADBD at 65 w/cm2 in an atmosphere of N2 and acetylene; 100 ppm acetylene.
Two samples of each film were prepared and each sample was left without further treatment for a 10 day period. At the end of that period of time, one sample of each film was corona treated at 50 m/min; the other was not.
All films were subjected to an ink adhesion test using a Sericol ink in a UV Flexo process followed by a scratch test. The scratch test was conducted using a nickel coin held at approximately 45 degrees and dragged away from the tester.
The results are presented in Table 1, wherein ink adhesion is measured on a scale of 1 to 3 (1 being relatively good and 3 being relatively poor). “N/A” indicates complete non-adhesion of the ink.
The results demonstrate that in relation to the control sample, corona treatment of the film makes no marked difference to the film's ink adhesion performance. In contrast, films treated by MADBD and then aged (by 10 days) show a marked improvement in ink adhesion performance upon corona treatment.
The film of example 1 was taken and MADBD treated in an atmosphere of nitrogen/acetylene; 200 ppm acetylene at 65 w/cm2. The resulting film after brief exposure to the atmosphere (Example 7) was then surface characterised by XPS spectroscopy to determine the relative atomic concentration of polar species at its surface. The film was then re-tested by the same technique after being aged for 2 weeks (Example 8).
The results are presented in Table 2.
The total relative atomic concentration of polar species measurable at the film surface by XPS spectroscopy was 11.4% immediately after MADBD treatment, and 10.5% after aging of the film for two weeks, representing a significant deterioration in the ability of the film to bind a UV flexo ink, for example.
Subsequent corona treatment of the aged film causes the relative atomic concentration of polar species measurable at the film surface to rise to 11.2%.
The film of example 1 was taken and MADBD treated in an atmosphere of nitrogen/acetylene; 75 ppm acetylene at 65 w/cm2. The treated film was aged for a period of approximately 2 months (Example 9) and then the resulting film was surface characterised by XPS spectroscopy to determine the relative atomic concentration of polar species at its surface. The film was then re-tested by the same technique after being aged for approximately 10 months (Example 10).
The results are presented in Table 3.
A film sample of the same type as used as the control sample in Examples 1 to 6 was taken and subjected to MADBD at 65 w/cm2 in an atmosphere of N2 and acetylene; 75 ppm acetylene.
The treated film was aged for a period of six months and then its surface energy was measured using dyne solutions from Sherman.
The aged film was then corona treated at 0.3 kW and 20 meters per minute and its surface energy measured again.
The results are presented in Table 4:
The results indicate that the surface energy of the film following MADBD treatment and subsequent aging can be re-boosted following corona treatment.
The films of Examples 2 to 6 are subjected to extraction tests according to the protocol described in the US Code of Federal Regulations, Title 21 Food and Drugs, Chapter I—Food and Drug Administration, Department of Health and Human Services, Part 177, Section 1520 Olefin Polymers (Edition: Apr. 1, 2012). The films are found to conform to the limits for maximum extractable fraction in n-hexane (i.e. not more than 6.4% at reflux temperature) and maximum soluble fraction in xylene (i.e. not more than 9.8% at 25° C.) for polypropylene as laid down in the Regulations.
The films of Examples 2 to 6 are also subjected to migration tests with food-simulating liquids using the test methods described in European Standard EN 1186:2002 (Parts 1-15). The films show an overall migration of less than 10 mg/dm2.
Thus, the films of Examples 2 to 6 are suitable for regulatory food contact approval in the US and Europe.
A biaxially oriented polymeric film having a core layer of polypropylene and coextruded polyolefin skin layers was manufactured by means of a bubble process. The film was MADBD treated in an atmosphere of nitrogen/acetylene; 200 ppm acetylene at 65 kW/m2·min. The resulting film was aged for 6 weeks and subsequently corona treated at 0.5 kW and 30 m/min. Samples of the film were printed by one of three methods:
i. UV Flexo using an Optiflex® ink
ii. UV Screen using an Optiscreen® ink
iii. UV Flexo/Screen Combination
Each printed sample was subjected to an ink pull-off tape test and scratch test (as previously described); a ruckle test wherein opposite edges of the sample were manually held and the sample was scrunched and then rubbed together at speed in a motion akin to pedals on a bike, for several seconds; and an appearance assessment. These tests were carried out as soon as the printed sample came off the press i.e. 0 hours after printing, and 24 hours thereafter.
The results are presented in Table 5, wherein each of the parameters tested is measured on a scale of 1 to 3 (1 being relatively good and 3 being relatively poor).
From the results it can be seen that good print quality is achieved using all three printing methods on the polypropylene-based film.
The film of Example 14 is subjected to the US and European food contact tests as outlined in Example 13.
The film is found to conform to the limits for maximum extractable fraction in n-hexane (i.e. not more than 6.4% at reflux temperature) and maximum soluble fraction in xylene (i.e. not more than 9.8% at 25° C.) for polypropylene as laid down in the US Regulations. It is also found that the film shows an overall migration of less than 10 mg/dm2 as required by European Standard EN 1186:2002 (Parts 1-15).
Thus, the film is suitable for regulatory food contact approval in the US and Europe.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1305631.2 | Mar 2013 | GB | national |
This application is a national stage application of International Patent Application No. PCT/GB2014/050987, filed Mar. 27, 2014, which claims priority to United Kingdom patent Application No. 1305631.2, filed Mar. 27, 2013. The entirety of the aforementioned applications is incorporated herein by reference.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/GB2014/050987 | 3/27/2014 | WO | 00 |
