Patent Application
20230151166
The present disclosure relates to a thin film for waste packing cassettes.
This section provides background information related to the present disclosure which is not necessarily prior art.
A lot of waste products produce smells that are annoying to the environment. Examples are decayed food, kid nappies and cat litter.
In the prior art there are many films that could be used for protection from malodors. As well known in the art, the use of materials like EVOH, PVDC, polyacrylonitrile is recommended in order to not allow malodors escape from the container (e.g. bag or another configuration) and create an unpleasant atmosphere.
There are also a lot of known configurations of packing a certain length of film (e.g. 20 meters) in a compressed form (e.g. in a cassette). Examples of the representative cassettes are shown in US 4,934,529 or US 3,536,192.
Generally, the cassette comprises a tubular core, casing wall and cassette bottom. The film is pulled through the area between the lid of the cassette and the casing wall. The flexible tubing is dispensed from the cassette. After the malodorous item is thrown into the bag the core is rotated and the flexible tube is twisted so that it closes as hermetically as possible the waste/environment area.
To dispose the next diaper, the user pulls the next portion of film. The previous hermetically closed diaper is pulled downwards and the new diaper is packed in a new configuration. All these different packs are stored in a bin which is periodically emptied.
Separation of one pack to the other can be done by various means. A rotary knife is preferred.
In the prior art a lot of possible film configurations either monolayer or multilayer have been proposed. The basic characteristics a film should have in order to be used in the particular case are:
With new environmental rules promoting the concept of “less plastic”, it is critical to produce films with lower thickness. At the same time, it is imperative that these films keep excellent barrier and mechanical properties.
Patent application EP 2085216 gives an example of production of successful films for this application. However, it is challenging to produce films with lower weight than 14 g/m2 as the bubble stability of the hot blown film is compromised. Further, the use of substantial non resilient material increases the possibility to have increased die lip deposits (die drool). Further, the use of such materials may not allow the coefficient of friction to go to as low as 0.2 (kinetic coefficient of friction, film to film, ASTMD 1894) which is often desired in such applications.
For example, films according to EP 2085216 have kinetic coefficient of friction (film to film and measured as per ASTM D1894) of more than 0.30 which creates serious issues during filling of the cassettes or in the use of the film or cassette by the consumer.
Further, the films according to EP 2085216 cannot be downgaged easily to as thin as 10 g/m2 which is a desirable effect for environmental reasons as long as mechanical properties are adequate.
We have surprisingly found that all the features required for such application can be achieved with a film comprising polyethylene from renewable biobased sources.
This section provides a general summary of the disclosure, and is not a comprehensive disclosure of its full scope or all of its features.
The invention is referring to a multilayer plastic film with weight less than 20 g/m2 for use in malodorous item packaging, wherein the film comprises at least 20% of biobased polyethylene and further comprises an odor barrier polymer.
In a first aspect the invention is directed to a multilayer film with weight less than 20 g/m2 for use in malodorous item packaging, wherein the film comprises two outer layers, wherein at least one of the outer layers comprise at least 20% of biobased polyethylene based on the total weight of the corresponding layer and wherein the film comprises at least one barrier layer comprising a polymer selected from polyamide, polyester and/or EVOH.
In a further aspect of the invention both outer layers comprise at least 50% per weight biobased polyethylene..
The multilayer preferably comprises in the barrier layer EVOH.
The total amount of substantially non-resilient material in the multiplayer film is preferably 50% per weight or less, more preferably 35% per weight or less, even more preferably 20% per weight or less.
According to a preferred the multilayer film has a weight less than 18 g/m2, preferably less than 17 g/m2, more preferably less than 16 g/m2, even more preferably less than 15 g/m2, most preferably less than 14 g/m2, and in particular less than 13 g/m2.
Preferably, the biobased polyethylene is selected among low density polyethylene, ethylene alpha olefin copolymer (preferably butene, hexene or octene copolymer), and high density polyethylene.
The biobased polyethylene comprised in at least one of the two outer layers has preferably a density of at least 0.900 g/cm3, more preferable at least 0.910, more preferably at least 0.915.
In a preferred embodiment the multilayer film further comprises at least one intermediate layer comprising polyamide, preferably the polyamide is polyamide 6 or polyamide 6/66.
In a preferred embodiment of the multilayer film at least one or both of the outer layer comprise a slip agent, preferably, the slip agent is an amide-based slip agent.
In the multilayer film of the present invention both outer layers have a kinetic film-to-film coefficient of friction of less than 0.35 measured according to ASTMD1894, preferably the coefficient of friction is less than 0.30, more preferably the coefficient of friction is less than 0.25, even more preferably less than 0.2.
In a preferred embodiment the multilayer film comprises, preferably consists of the following layers: OUTER LAYER / INTERMEDIATE LAYER 1 / BARRIER LAYER / INTERMEDIATE LAYER 3 / OUTER LAYER wherein INTERMEDIATE LAYER 1 and 3 can comprise the same or different materials.
In a further preferred embodiment, the multilayer film comprises, preferably consists of the following layers: OUTER LAYER / INTERMEDIATE LAYER 1 / INTERMEDIATE LAYER 2 / BARRIER LAYER / INTERMEDIATE LAYER 3 / INTERMEDIATE LAYER 4 / OUTER LAYER wherein each of INTERMEDIATE LAYER 1-4 can comprise the same or different materials.
In a preferred embodiment the multilayer film presents an antibacterial activity characterized by a decline of at least 20% of the population of Staphylococcus aureus held in contact with at least one of the outer layers of the film for 24 hours compared to the initial population, measured according to ISO 2196/2011 for measurement of the antibacterial activity on plastics and other non-porous surfaces.
In a preferred embodiment the multilayer film at least one of the outer layers, preferably both outer layers, additionally comprise 0.5-40% per weight, preferably 5-30% per weight low density polyethylene (LDPE) based on the total weight of the corresponding outer layer.
According to a second aspect a cassette is provided comprising a multilayer film according to the present invention.
A third aspect of the invention related to the use of a multilayer film according to the present invention for waste packing.
Preferably, the film is stored in a cassette.
In a preferred embodiment the film is folded or the film is in the form of a bag.
In this application the following definitions are used:
The term “film” refers to a flat or tubular flexible structure of thermoplastic material.
The term “heat shrinkable” refers to a film that shrinks at least 10% in at least one of the longitudinal and transverse directions when heated at 90° C. for 4 seconds. The shrinkability is measured in water according to ASTM 2732. For temperatures like 100° C. or more, glycerine is used as a reference liquid.
The term “total heat shrinkability” refers to the sum of heat shrinkability at the MD direction and heat shrinkability at the TD direction. In all cases, ASTM 2732 is used for measurement of shrinkabilities.
The term “multilayer” refers to a film comprising 2 or more layers.
The phrase “longitudinal direction” or “machine direction” herein abbreviated “MD” refers to a direction along the length of the film.
The phrase “outer layer” refers to the film layer which comes in immediate contact with the outside environment. Therefore, the film has two outer layers, and when formed to a pack one of outer layers is inside of the pack and one at the outside of the pack.
The phrase “inner layer” refers to any film layer that is not “outer layer».
As used herein, the term “homopolymer” refers to a polymer resulting from polymerization of a single monomer.
As used herein, the term “copolymer” refers to a polymer resulting from polymerization of at least two different polymers.
As used herein, the term “polymer” includes both above types.
As used herein, the term “polyolefin” refers to any polymerized olefin, which can be linear, branched, cyclic, aliphatic, substituted or unsubstituted. More specifically, included in the term polyolefin are homopolymers of olefin, copolymers of olefin, copolymers of an olefin and a non-olefinic comonomer (such as ester) etc. Specific examples include polyethylene homopolymer, polypropylene homopolymer, polybutene homopolymer, ethylene alpha olefin copolymer, propylene alpha olefin copolymer, butene alpha olefin copolymer, ionomer, ethylene ester copolymer etc.
As used herein the term “polyethylene” identifies polymers consisting essentially of the ethylene repeating unit. The homopolymers of ethylene that have a density more than 0.940 are called high density polyethylene (HDPE), the ones that are have less than 0.940 are low density polyethylene (LDPE).
As used herein the phrase “ethylene alpha olefin copolymer” refers to ethylene-based copolymers like linear low-density polyethylene (LLDPE), medium density polyethylene (MDPE), very low-density polyethylene (VLDPE), ultra-low-density polyethylene (ULDPE), metallocene catalyzed polymers and polyethylene plastomers and elastomers.
As used herein the term “homogeneous ethylene alpha olefin copolymers” refer to ethylene alpha olefin copolymers having a molecular weight distribution less than 2.7 as measured by GPC. Typical examples of these polymers are AFFINITY from DOW or Exact from Exxon.
As used herein the phrase “styrene polymers” refers to styrene homopolymer such as polystyrene and to styrene copolymers such as styrene-butadiene copolymers, styrene-butadiene-styrene copolymers, styrene-isoprene-styrene copolymers, styrene-ethylene-butadiene-styrene copolymers, ethylene-styrene copolymers and the like.
As used herein the term “biobased polyethylene” or “polyethylene from renewal sources” refers to a polyethylene of which the building blocks eg monomers are produced from non-fossil fuels. A typical example is a polyethylene of which the ethylene is produced from naphtha not of fossil fuel origin but alternatively from tall oil origin or cooked oil origin. Production of such biobased naphtha eg by hydrotreatment is known in the art.
As used herein the phrase “ethylene methacrylate copolymers” refers to copolymers of ethylene and methacrylate monomer. The monomer content is less than 40%.
As used herein the phrase “ethylene vinyl acetate copolymer” or EVA refer to copolymers of ethylene and vinyl acetate.
As used herein the phrase “ethylene ester copolymer” includes any polymer made from ethylene and ester monomers. It is obvious that this term includes EVAs, EMAs and other polymers.
As used herein the term “odor barrier polymer” refers to polymers which have the property to limit the passage of odor through a film or a layer comprising the polymer. Such materials are EVOH, PVDC, polyamide or polyester.
As used herein, the term EVOH refers to saponified products of ethylene vinyl ester copolymers. The ethylene content is typically in the range of 25 to 50% per mol. All the later references to EVOH ethylene content will be in % per mol.
As used herein the term PVDC refers to a vinylidene chloride copolymer wherein a major amount of the copolymer comprises vinylidene chloride and a minor amount of the copolymer comprises one or more monomers such as vinyl chloride and/or alkyl acrylates and methacrylates.
As used herein the term “polyamide” refers to homopolymers and copolymers. Polyamide 6, polyamide 66, polyamide 12, polyamide 6/66, polyamide 6/12, polyamide elastomers, MXD polyamides and other copolymers are specifically useful for the invention.
As used herein the term “polyester” refers to polymers comprising terephthalate units. Examples of polyesters are PET (polyethylene terephthalate), PBT (polybutylene terephthalate), polyester elastomer (block copolymer comprising ester or ether units), PTT and other similar polymers.
As used herein, the term “ionomer” comprises the copolymers of ethylene and methacrylic or acrylic acid being metal neutralized. An example of such material is Surlyn from Dupont.
As used herein, the term “polypropylene” refers to polymers incorporating propylene structural units in a weight percentage of more than 50% per weight of the total polymer. Examples of these, are homo polypropylenes, random copolymers of propylene and ethylene, block copolymers of propylene and ethylene, copolymers or blends of propylene and rubber (such as blends of polypropylene and ethylene propylene rubber), propylene ethylene alpha olefin terpolymers and others.
These polymers may be isotactic, syndiotactic or atactic. Isotactic is preferred.
As used herein the term “substantially non resilient material” refers to materials or material compounds comprising inorganics like calcium carbonate, titanium dioxide, wollastonite, mica, glass fibers, dolomite, silica and the like.
All measurement methods mentioned herein are readily available for the skilled person. For example, they can be obtained from the American National Standards Institute at: www.webstore.ansi.org.
All percentages are based on weight per weight ratio, except when otherwise stated.
Further areas of applicability will become apparent from the description provided herein. The description and specific examples in this summary are intended for purposes of illustration only and are not intended to limit the scope of the present disclosure.
Example embodiments will now be described more fully with reference to the accompanying drawings.
According to a first aspect the present invention is directed to a multilayer film with weight less than 20 g/m2 for use in malodorous item packaging, where the film comprises two outer layers comprising ethylene alpha olefin copolymers.
In a preferred embodiment the multilayer film comprises, preferably consists of the following layers: OUTER LAYER / INTERMEDIATE LAYER 1 / INTERMEDIATE LAYER 2 / BARRIER LAYER / INTERMEDIATE LAYER 3 / INTERMEDIATE LAYER 4 / OUTER LAYER wherein each of INTERMEDIATE LAYER 1-4 can comprise the same or different materials.
In a preferred embodiment the multilayer film comprises, preferably consists of the following layers: OUTER LAYER / INTERMEDIATE LAYER 1 / BARRIER LAYER / INTERMEDIATE LAYER 3 / OUTER LAYER wherein INTERMEDIATE LAYER 1 and 3 can comprise the same or different materials.
Preferably, the multilayer film comprises an odor barrier layer.
In one embodiment the barrier layer comprises EVOH as an odor barrier material.
The EVOH used preferably has an ethylene content less than 48%, more preferably less than 44%, more preferably less than 38%, more preferably from 27 to 32% ethylene.
In another embodiment the barrier layer comprises polyamide as a barrier material.
The oxygen barrier material preferably has a weight of less than 5 g/m2, more preferably less than 4 g/m2 , even more preferably less than 2.5 g/m2.
The outer layer comprises preferably at least 20% of biobased polyethylene. In a preferred version, both outer layer comprises at least 50% biobased polyethylene.
The biobased polyethylene is preferably low density polyethylene, ethylene alpha olefin copolymer, medium density polyethylene and/or high density polyethylene.
In a preferred embodiment the biobased polyethylene is used in blend with ethylene alpha olefin copolymer, preferably butene, hexene or octene copolymer.
In a further preferred embodiment at least one of the outer layers, preferably both outer layers, additionally comprises 0.5-40%, preferably 5-30% per weight low density polyethylene (LDPE) based on the total weight of the corresponding outer layer.
In a further preferred embodiment at least one of the outer layers comprises high density polyethylene.
In a further preferred version, the weight of each outer layer is less than 8 g/m2, preferable less than 6 g/m2, more preferably less than 5 g/m2.
The total amount of substantially non-resilient material in each outer layer is preferably 50% per weight or less, more preferably 40% per weight or less, even more preferably 30% per weight or less.
In a preferred version, at least one or both of the outer layer comprise a slip agent, preferably, the slip agent is an amide-based slip agent (lubricant).
Slip agents are preferable of the amide family, such as erucamide, oleamide, oleyl-palmitamide, stearamide, behenamide and the like. Alternatively, the slip may also comprise silicon or siloxane materials.
In a further preferred version of the invention the kinetic coefficient of friction of each of the two outer layers measured upon itself (as per ASTMD1894) is less than 0.35, more preferably less than 0.3, even more preferably less than 0.25, most preferably less than 0.2.
In a preferred embodiment, the multilayer film comprises at least one intermediate layer. The multilayer film can comprise several intermediates layers. Preferably the intermedial layer(s) is (are) located between the barrier layer and one of the outer layers. There can be more than one intermediate layer be located between the barrier layer and one of the outer layers.
In the intermediate layers, typical adhesive resins like maleic anhydrite modified polyolefins may be used. Typical examples are BYNEL from Dupont and OREVAC from Arkema.
In another preferred version of the invention, an intermediate layer comprises a polyamide. For example, a preferred version of the invention is:
In another version of the invention, at least one intermediate layer comprises polyamide.
If a multilayer film of the present invention comprises polyamide in an intermediate layer, then preferably polyamide 6 or polyamide 6/66 is used.
In another preferred version of the invention the adhesive tie layers are compounds of biobased polyethylene eg with maleic anhydride.
Additives well known in the art may be used in one or more layers of the present invention. Slip additives, antifog additives, polymer processing aids may be used if pertinent. Antimicrobial and/or antibacterial additives may also be used in one or more of the layers to inhibit the microbe formation. Preferably the antimicrobial or antibacterial additive is added to at least one, or both outer layers. Preferably the antimicrobial or antibacterial additive is added to the outer layer in direct contact to the product to be packed.
The antimicrobial/antibacterial additive preferably comprises silver, silver ion and/or copper. More preferably it comprises silver ion.
The additive may be used in an amount of from 0.2 to 20% per weight of the corresponding layer wherein the additive is added.
In a preferable version of the invention the film comprises polypropylene, more preferable biobased polypropylene.
The total amount of substantially non-resilient material in the multilayer film is preferably 30% per weight or less, more preferably 20% per weight or less.
The total amount of substantially non-resilient material in each outer layer is preferably 30% per weight or less, more preferably 20% per weight or less.
In a preferable version of the invention the film presents an antibacterial activity as follows; a decline of at least 20% of the population of Staphylococcus aureus held in contact with at least one of the outer layers of the film for 24 hours compared to the initial population. The measurements are made as per ISO 2196/2011 measurement of the antibacterial activity on plastics and other non-porous surfaces.
In order to increase the mechanical properties, the film may be crosslinked with one of the following methods. E-beam radiation, gamma radiation, moisture crosslinking using silane grafting compounds, peroxide crosslinking.
The film may be in tubular form or sealed at the edges or single sheet configuration. It may also be folded once or many times (as per US 5,037,370 for example). It can also be used in the form of a series of bags, gusseted or non-gusseted, folded or not folded. Centerfold configuration is also possible.
The preferred production method for the film is the hot blown film method, which is well known in the art. Other methods like extrusion through flat cast die is also possible.
In a preferable embodiment the film is stored in a cassette prior to use, e.g. a cassette as described in US 4,934,529.
According to a second aspect the present invention is directed to a cassette comprising a film according to the present invention for use in waste packaging applications. In a preferable embodiment a cassette as described e.g. in US 4,934,529 is used.
According to a third aspect the present invention is directed to the use of a multilayer film according to the present invention for waste packing, wherein the film is preferably stored in a cassette.
In a preferable embodiment the film is stored in a cassette prior to use, e.g. a cassette as described in US 4,934,529.
A 5-layer film is produced in a commercial hot blown film line with the following recipe:
The thickness of the structure is 7.5/1.5/1.5/1.5/6 starting from the outer layer1 and going to the outer layer 2.
The weight of the film is 17.1 g/m2.
A 5-layer film is produced in a hot blown film commercial line with the following recipe:
The thickness of the structure is 6.5/1.5/1.5/1.5/5 starting from the outer layer 1 and going to the outer layer 2.
The weight of the material is 15.102 g/m2.
A 5-layer film is produced in a hot blown film commercial line with the following recipe:
The thickness of the structure is 3/1.5/1.5/1.5/3 starting from the outer layer 1 and going to the outer layer 2.
The weight of the material is 10.068 g/m2.
The difference between examples 1, 2 on one hand and example 3 on the other hand is that in examples 1, 2 a biobased polyethylene produced by wood residue was used while in example 3 a biobased polyethylene produced by cooked oil residue was used. Both biobased Pes were of the same density and chemical structure.
A 5-layer film is produced in a hot blown film commercial line with the following recipe: exactly same as example 1 but the biobased PE is replaced by the same grade PE from fossil fuel building blocks.
A 5-layer film is produced in a hot blown film commercial line with the following recipe : exactly same as example 3 but the biobased PE is replaced by the same grade PE from fossil fuel building blocks.
It was surprisingly found that the examples comprising polyethylene of biobased content are easier to downgage to the very low film thicknesses as required by the application.
More specifically the number of bubble bursts (i.e. bubble is collapsing and the extrusion process is interrupted) was monitored per each case. Reference was 10 hours of steady production during which the blown film behavior was watched and the bubble bursts were recorded.
A paper core of diameter 76 mm and height 50 cm was used in order to test compression.
Around the diameter of paper core, a tubular film was placed and squeezed. The film length was measured so that the film did not overpass the upper end of the core. This test represents how easy is to put the tubular film in the cassette (so the number of film meters that can be squeezed inside).
By completing the test it was obvious that the result of the testing is the same independently of the biobased or not biobased sourcing of the polyethylene.
The foregoing description of the embodiments has been provided for purposes of illustration and description. It is not intended to be exhaustive or to limit the disclosure. Individual elements or features of a particular embodiment are generally not limited to that particular embodiment, but, where applicable, are interchangeable and can be used in a selected embodiment, even if not specifically shown or described. The same may also be varied in many ways. Such variations are not to be regarded as a departure from the disclosure, and all such modifications are intended to be included within the scope of the disclosure.
| Number | Date | Country | Kind |
|---|---|---|---|
| EP21208221.8 | Nov 2021 | EP | regional |
