NZ742977B - Prestretched balewrap - Google Patents
Prestretched balewrapInfo
- Publication number
- NZ742977B NZ742977B NZ742977A NZ74297716A NZ742977B NZ 742977 B NZ742977 B NZ 742977B NZ 742977 A NZ742977 A NZ 742977A NZ 74297716 A NZ74297716 A NZ 74297716A NZ 742977 B NZ742977 B NZ 742977B
- Authority
- NZ
- New Zealand
- Prior art keywords
- film
- prestretched
- polyethylene film
- lldpe
- polyethylene
- Prior art date
Links
- -1 polyethylene Polymers 0.000 claims abstract description 131
- 239000004698 Polyethylene (PE) Substances 0.000 claims abstract description 128
- 229920000573 polyethylene Polymers 0.000 claims abstract description 128
- 239000004707 linear low-density polyethylene Substances 0.000 claims abstract description 73
- 239000004460 silage Substances 0.000 claims abstract description 19
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-Octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims abstract description 17
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 claims abstract description 8
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-Hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000011954 Ziegler–Natta catalyst Substances 0.000 claims abstract description 7
- 239000002699 waste material Substances 0.000 claims abstract description 4
- 229920000092 linear low density polyethylene Polymers 0.000 claims description 48
- 239000000155 melt Substances 0.000 claims description 10
- 238000005530 etching Methods 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 235
- 239000000203 mixture Substances 0.000 description 90
- 239000000463 material Substances 0.000 description 19
- 229920000642 polymer Polymers 0.000 description 18
- 229920002367 Polyisobutene Polymers 0.000 description 15
- 239000003381 stabilizer Substances 0.000 description 15
- 239000000049 pigment Substances 0.000 description 12
- 229920000098 polyolefin Polymers 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 10
- 239000004708 Very-low-density polyethylene Substances 0.000 description 9
- 229920001866 very low density polyethylene Polymers 0.000 description 9
- 239000005038 ethylene vinyl acetate Substances 0.000 description 8
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- 229920001684 low density polyethylene Polymers 0.000 description 5
- 239000004702 low-density polyethylene Substances 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000035699 permeability Effects 0.000 description 4
- 210000001138 Tears Anatomy 0.000 description 3
- 230000000996 additive Effects 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 240000000218 Cannabis sativa Species 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 230000004059 degradation Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 239000010902 straw Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 241000271566 Aves Species 0.000 description 1
- 210000003323 Beak Anatomy 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 102100016444 CCDC50 Human genes 0.000 description 1
- 101710023985 CCDC50 Proteins 0.000 description 1
- 210000000078 Claw Anatomy 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 101710032250 MICAL1 Proteins 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- ORECYURYFJYPKY-UHFFFAOYSA-N N,N'-bis(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine;2,4,6-trichloro-1,3,5-triazine;2,4,4-trimethylpentan-2-amine Chemical compound CC(C)(C)CC(C)(C)N.ClC1=NC(Cl)=NC(Cl)=N1.C1C(C)(C)NC(C)(C)CC1NCCCCCCNC1CC(C)(C)NC(C)(C)C1 ORECYURYFJYPKY-UHFFFAOYSA-N 0.000 description 1
- 229920001748 Polybutylene Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229940035295 Ting Drugs 0.000 description 1
- 241000424123 Trachinotus baillonii Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- VOLSCWDWGMWXGO-UHFFFAOYSA-N cyclobuten-1-yl acetate Chemical compound CC(=O)OC1=CCC1 VOLSCWDWGMWXGO-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent Effects 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable Effects 0.000 description 1
- 238000010096 film blowing Methods 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000006011 modification reaction Methods 0.000 description 1
- 230000001473 noxious Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- YCTDZYMMFQCTEO-UHFFFAOYSA-N oct-3-ene Chemical compound CCCCC=CCC YCTDZYMMFQCTEO-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000000717 retained Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01F—PROCESSING OF HARVESTED PRODUCE; HAY OR STRAW PRESSES; DEVICES FOR STORING AGRICULTURAL OR HORTICULTURAL PRODUCE
- A01F15/00—Baling presses for straw, hay or the like
- A01F15/07—Rotobalers, i.e. machines for forming cylindrical bales by winding and pressing
- A01F15/071—Wrapping devices
- A01F15/0715—Wrapping the bale in the press chamber before opening said chamber
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01F—PROCESSING OF HARVESTED PRODUCE; HAY OR STRAW PRESSES; DEVICES FOR STORING AGRICULTURAL OR HORTICULTURAL PRODUCE
- A01F15/00—Baling presses for straw, hay or the like
- A01F15/07—Rotobalers, i.e. machines for forming cylindrical bales by winding and pressing
- A01F15/071—Wrapping devices
- A01F2015/0745—Special features of the wrapping material for wrapping the bale
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0018—Combinations of extrusion moulding with other shaping operations combined with shaping by orienting, stretching or shrinking, e.g. film blowing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/07—Flat, e.g. panels
- B29C48/08—Flat, e.g. panels flexible, e.g. films
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/16—Articles comprising two or more components, e.g. co-extruded layers
- B29C48/18—Articles comprising two or more components, e.g. co-extruded layers the components being layers
- B29C48/21—Articles comprising two or more components, e.g. co-extruded layers the components being layers the layers being joined at their surfaces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/04—Polymers of ethylene
- B29K2023/06—PE, i.e. polyethylene
- B29K2023/0608—PE, i.e. polyethylene characterised by its density
- B29K2023/0625—LLDPE, i.e. linear low density polyethylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/04—Polymers of ethylene
- B29K2023/08—Copolymers of ethylene
- B29K2023/083—EVA, i.e. ethylene vinyl acetate copolymer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0005—Condition, form or state of moulded material or of the material to be shaped containing compounding ingredients
- B29K2105/0044—Stabilisers, e.g. against oxydation, light or heat
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2509/00—Use of inorganic materials not provided for in groups B29K2503/00 - B29K2507/00, as filler
- B29K2509/02—Ceramics
-
- 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
- B32B2270/00—Resin or rubber layer containing a blend of at least two different polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/514—Oriented
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/514—Oriented
- B32B2307/516—Oriented mono-axially
-
- 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
- B32B2410/00—Agriculture-related articles
-
- 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
- B32B27/306—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)polymers
-
- 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
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- 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
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
- B32B27/327—Layered products comprising a layer of synthetic resin comprising polyolefins comprising polyolefins obtained by a metallocene or single-site catalyst
Abstract
prestretched polyethylene film having a longitudinal degree of pre-stretching above 70% and a remaining longitudinal elongation capability of at least 300% as determined according to ASTM D882, wherein said film is a coextruded blown film comprising at least one core layer arranged between two exterior layers, wherein the thickness of the film is in the range of 10-30 μm, and wherein the film comprises at least 25% by weight of a linear low density polyethylene (LLDPE) substantially free from long chain branching (LCB) produced using a Ziegler Natta catalyst and hexene, heptene or octene as comonomer and having a density of between 910 and 915 kg/m3. Use of the prestretched polyethylene film as an agricultural balewrap film or silage film, pallet wrapping film, or waste wrap film. erior layers, wherein the thickness of the film is in the range of 10-30 μm, and wherein the film comprises at least 25% by weight of a linear low density polyethylene (LLDPE) substantially free from long chain branching (LCB) produced using a Ziegler Natta catalyst and hexene, heptene or octene as comonomer and having a density of between 910 and 915 kg/m3. Use of the prestretched polyethylene film as an agricultural balewrap film or silage film, pallet wrapping film, or waste wrap film.
Description
PRESTRETCHED BALEWRAP
FIELD OF THE INVENTION
The present invention relates to a prestretched agricultural stretch wrap film
suitable for baling ations, such as for example packaging grass, maize,
sugar beet pulp, malt, straw, household refuse, and the like.
BACKGROUND OF THE INVENTION
Plastic film is used for many different es. For example, plastic stretch
film is ntly used in different fields of application, in particular for
wrapping various products, for e wrapping goods for shipping or
storing, or for wrapping agricultural bulk products, such as grass, straw,
s crops, etc. In agricultural applications, stretch film may for instance be
used as fodder protection and silage film. For the production of silage,
anaerobic ions are desirable, and so the film should provide a barrier
against moisture and oxygen.
In silage tion, a baler is first used to form compact bales of the
agricultural bulk product, which are wrapped tightly with net, twine or film to
retain the shape of the bale. Once the net, twine or film is lying around the
bale, the formed bale is ejected from the baling chamber.
The bale is then wrapped with an agricultural stretch wrap film using a bale
wrapper. In the bale wrapper the agricultural stretch wrap film is stretched,
typically in the range of 50-75% and a number of layers of the stretched
agricultural stretch wrap film are wrapped around the bale to form an airtight
and waterproof bale suitable for silage production.
Conventionally, agricultural stretch wrap films are made primarily of one or
more polymers, in particular efins (e.g. polyethylene). The polyolefin is
extruded and blown to form a tubular film. Usually various additives such as
pigments, tackifiers, UV stabilizers, etc, are added to the film composition in
order to meet the requirements of the intended use. Stretch film for silage
productions es e.g. a good UV ization of the film al, high
cling, and high mechanical performance in terms of good resistance to
puncturing and tearing.
Agricultural stretch wrap films are often prestretched in the machine direction
(i.e. in the longitudinal direction) during manufacturing. Prestretching has
been shown to provide films with improved mechanical properties and lower
or maintained oxygen permeability compared to unstretched films of the same
film thickness. The etched film is then (further) stretched when used for
ng. Prestretching is advantageous because thinner films can be used,
which means e.g. less film material per bale, more s of) film per roll at
the same roll weight, and less frequent roll change.
It is thus tood that it is the higher the prestretching the greater the
savings. However, as identified in the International patent application
W02009040129A2 there are limitations in the degree of stretching which can
be d to the currently known prestretched agricultural stretch wrap films.
When a film is stretched in the bale wrapper, typically by approximately 50 to
75%, by means of the stretch unit provided on the bale wrapper it has been
found that the prestretched agricultural stretch wrap films which are
etched to a degree above 70% tear off more easily when stretched at
this standard stretch percentage of approximately 50 to 75%. Such tearing
results in time loss for the user, badly wrapped bales and an increase in the
use of film. To remedy this problem W02009040129A2 ts to use films
prestretched to a degree below 70%. This low degree of prestretching
obviously limits the potential advantages of higher prestretching, i.e. thinner
films, less film material per bale, more (metres of) film per roll at the same roll
weight, and less frequent roll change.
It is an object of the t invention to provide a prestretched agricultural
stretch wrap film which can be used as an alternative to the prior art
agricultural stretch wrap films which allow a higher degree of prestretching
(typically higher than 70%) without the abovementioned drawbacks of the
known prestretched agricultural stretch wrap films.
SUMMARY OF THE INVENTION
It is an object of the t invention to at least partly overcome the
problems in the prior art, and to provide a stretch film with properties
acceptable for use in agriculture and/or industry, which can be produced at a
relatively low cost.
According to a first aspect of the invention, this and other objects are
achieved by a prestretched polyethylene film having a longitudinal degree of
pre-stretching above 70% and a ing longitudinal tion capability
of at least 300% as determined according to ASTM D882, wherein the
thickness of the film is in the range of 10 - 30 um and wherein the film
comprises at least 25% by weight of a linear low density polyethylene
(LLDPE) ntially free from long chain branching (LCB) and having a
y below 915 kg/m3.
ing to preferred embodiments, there is provided a prestretched
polyethylene film having a longitudinal degree of pre-stretching above 70%
and a remaining longitudinal elongation capability of at least 300% as
determined according to ASTM D882, wherein said film is a coextruded blown
film comprising at least one core layer arranged between two or ,
wherein the thickness of the film is in the range of 10-30 pm, and wherein the
film comprises at least 25% by weight of a linear low density polyethylene
(LLDPE) substantially free from long chain branching (LCB) produced using a
Ziegler Natta catalyst and hexene, heptene or octene as comonomer and
having a density of between 910 and 915 kg/m3.
2016/082078
Prestretching of polyethylene films has been shown to provide films with
improved mechanical properties and lower or maintained oxygen permeability
compared to unstretched films of the same film thickness. Accordingly,
thinner films can be used, which means e.g. less film material per bale, more
(metres of) film per roll at the same roll weight, and less frequent roll change.
An additional advantage of the stretch film according to the present invention
is lower raw material costs.
The inventive film comprises at least 25% by weight of linear low density
polyethylene (LLDPE) substantially free from long chain branching (LCB) and
having a density below 915 kg/m3. Using this particular type of linear low
density polyethylene has been found to allow higher degrees of prestretching
with retained high tion capability, thus alleviating the prior art g
problems associated with films prestretched to a degree above 70%. The
inventive films have also been found to t similar or better mechanical
performance for use in agricultural bale wrapping ations, as compared
to the corresponding prior art films comprising higher density LLDPE instead
of the LLDPE substantially free from long chain branching (LCB) and having a
density below 915 kg/m3. The portion of the prestretched polyethylene film not
made up of the linear low density polyethylene (LLDPE) substantially free
from long chain branching (LCB) and having a density below 915 kg/m3 may
comprise other types of LLDPE, LDPE, and other polyolefins and additives
commonly used in the manufacture of prestretched polyethylene films.
According to some embodiments, prestretched polyethylene film comprises at
least 35%, ably in the range of 35-95%, by weight of said linear low
density hylene (LLDPE) substantially free from long chain ing
(LCB).
According to some embodiments, the etched polyethylene film
comprises a mixture of LLDPE substantially free from long chain branching
(LCB) and having a density below 915 kg/m3 and higher density LLDPE,
n the LLDPE mixture has a density below 916 kg/m3, preferably below
915 kg/m3, and more preferably below 914 kg/m3.
Prestretched polyethylene films are commonly produced from linear low
y polyethylene (LLDPE). LLDPE is used in stretch films due to its
favorable characteristics in respect of e.g. tensile strength, elongation at
break and puncture resistance. The LLDPE used in h wrap polyethylene
films, particularly films for agricultural applications, can be LLDPE prepared
using a Ziegler Natta or Philips type catalyst and a comonomer, such as
octene, to provide a suitable degree of short chain branching. This type of
LLDPE typically has a density of about 918 kg/m3. The LLDPE may also be
prepared using a ocene catalyst and a comonomer, such as .
Metallocene catalysts may lead to the formation of a small degree of long
chain branching (LCB) in addition to the short chain branching.
The LLDPE used in the inventive prestretched polyethylene films is preferably
LLDPE prepared using a Ziegler Natta type catalyst and a comonomer, such
as hexene, heptene or octene, or a e thereof, to provide a le
degree of short chain branching, and no or substantially no long chain
branching. The LLDPE used in the inventive prestretched polyethylene films
has a low density compared to LLDPE typically used in prior art stretch wrap
polyethylene films, particularly films for agricultural applications.
According to some ments, the linear low density polyethylene )
substantially free from long chain branching (LCB) is an LLDPE is produced
using a Ziegler Natta catalyst and hexene, heptene or octene or a mixture
f as comonomer. In preferred embodiments the comonomer is hexene
or octene. In more preferred embodiments the mer is octene.
Preferably, the linear low density polyethylene (LLDPE) substantially free
from long chain branching (LCB) comprises from about 85 wt% to about 98
wt% of recurring units of ethylene and from about 2 wt % to about 15 wt % of
recurring units of hexene, heptene or octene.
According to some embodiments, the linear low density polyethylene (LLDPE)
substantially free from long chain branching (LCB) has a density of between
910 and 915 kg/m3, preferably a density of between 911 and 913 kg/m3,
preferably a density of about 912 kg/m3.
According to some embodiments, the linear low density polyethylene (LLDPE)
substantially free from long chain branching (LCB) has a melt flow index (MI)
in the range of 0.7-1 .3 g/10min, preferably a melt flow index in the range of
0.9-1.1 g/10min, preferably a melt flow index of about 1 g/10min, as
determined according to ASTM D1238 at 190 °C with a 2.16 kg weight.
The expression prestretched polyethylene film means that the polyethylene
film is stretched in the longitudinal ion during the film production process
before being wound onto rolls. Stretching is typically performed in a prestretch
unit of the production line and involves passing the film between two or more
stretching rollers ng at different speeds. The prestretching may
preferably be performed directly after the extrusion or film blowing steps,
while the film is still hot. The degree of prestretching is intended to mean the
difference in speed, in t, between the stretching rollers in the prestretch
unit. The difference in speed corresponds to the elongation of the
prestretched film n the stretching rollers in the prestretch unit.
The prestretched polyethylene film has a longitudinal degree of prestretching
above 70%. The longitudinal degree of prestretching of the etched
polyethylene film may for example be n 70% and 150%, such as
between 70% and 125%, between or 70% and 100%.
According to some preferred embodiments, the prestretched polyethylene film
has a longitudinal degree of prestretching n 70% and 85%, preferably
between 71% and 79%, preferably between 73% and 77%, ably about
75%.
The term elongation capability as used herein means the elongation
2016/082078
tage at break, as measured in accordance with the ASTM D882
standard, wherein a strip of film with a width of 20 mm, clamped between two
clamps at a distance of 50 mm from each other is stretched at a rate of 500
mm/min until the film breaks. At least five strips of the film must be measured,
and the elongation capability corresponds to the mean value of the
measurements.
According to some embodiments, the prestretched hylene film has a
ing longitudinal elongation capability of at least 320%, preferably at
least 340%, as determined according to ASTM D882.
The stress required in order to stretch the prestretched film by 70% in the
longitudinal direction can be read from the tensile strength graph ed
when measuring the elongation percentage at break in accordance with the
ASTM D882 standard as described above. At least five strips of the film must
be measured, and the stress at 70% tion corresponds to the mean
value of the measurements.
According to some embodiments, the stress required in order to stretch the
prestretched polyethylene film by 70% in the longitudinal direction is less than
19 MPa, preferably less than 18 MPa, as determined according to ASTM
D882.
According to some embodiments, the thickness of the film is in the range of
13-25 pm, preferably in the range of 15-20 pm.
Typically, the stretch film according to embodiments of the present invention
allows an anaerobic environment to be formed and y nutrients and
energy content to be preserved during storage. A silage film should form a
barrier for oxygen gas. lly, a silage film has an oxygen permeability of
less than 10 000 cm3/m2/24 h, such as within the range of from 1000 to 10
000 cm3/m2/24 h measured according to the standard ASTM D-1434.
By the term “UV stabilization” is meant protection of a al from the long-
term degradation effects from light, most frequently ultraviolet radiation (UV).
By the term nical performance” is herein mainly meant the mechanical
strength of the material, measured in terms of at least one of tensile strength,
tear th and re resistance. Tensile strength, measured as force
per unit area, is defined as the maximum stress that a material can withstand
while being stretched or pulled before failing or breaking. Tear strength,
typically measured as force per unit length, is defined as the resistance of a
material to the growth of e.g. a cut when under tension. Elongation at break is
defined as the ultimate elongation (given as percentage of the initial length) of
a material before it breaks under tension. Puncture resistance, typically
measured as mass per unit length, is d as the relative ability of a
al to withstand a falling dart without breaking.
According to an embodiment, the prestretched polyethylene film is a
coextruded multi-layer blown film comprising at least two layers. Preferably,
the etched polyethylene film is a multi-layer film comprising at least
three layers: at least one core layer arranged between two exterior layers.
According to an embodiment, at least one layer comprises in the range of 40-
99% by weight of the linear low density polyethylene (LLDPE) substantially
free from long chain branching (LCB). According to an embodiment, the at
least one core layer comprises in the range of 40-99% by weight of the linear
low density polyethylene (LLDPE) substantially free from long chain
branching (LCB).
According to an embodiment, at least one of the two exterior layers comprises
a soft r. A soft polymer may provide a relatively soft surface to the at
least one of the two exterior layers which may increase friction, and reduce
slip in a direction ntially el to the film surface. A soft polymer may
be advantageous when the prestretched polyethylene film is e.g. wrapped
with an p, such that the film may adhere, or cling, to itself. By the term
“cling” is meant the ability of a material to adhere to itself or an nt
object. The adjacent object may be a layer of the same or a different film.
According to an embodiment, the prestretched hylene film may
comprise a tackifier. By the term “tackifier” is herein meant an agent that
provides cling to a film. Such an agent may be added to a layer of the
prestretched polyethylene filmin order to increase the cling of the layer. For
instance, a tackifier may be a soft polymer, or a migrating tackifier. A tackifier
thus serves to increase the cling of the prestretched polyethylene film, in
particular, of the or layers.
According to an embodiment, the tackifier is a migrating tackifier. By the term
“migrating tackifier” is herein meant a tackifier which is e in the film
material, e.g. in polyethylene. If a migrating tackifier is added to a film (or film
layer) in an amount exceeding the solubility level of the film (or film layer), the
excess can migrate within the film material to the film surface (including also
migrating from a first layer to and through a r layer, when the first layer
has been saturated with the migrating tackifier). A migrating tackifier may thus
e an adhesive surface which increases the friction in a direction
substantially perpendicular to the film surface. A migrating tackifier may be
advantageous when the prestretched polyethylene film is e.g. wrapped, such
that an exterior layer of a first portion of the prestretched polyethylene film
adhere, or cling, to an or layer of a second portion of the same, or a
different, etched polyethylene film.
According to an embodiment, the migrating tackifier is present at a content of
from 1 to 15% by weight based on the total weight of the at least one core
layer. The content of migrating tackifier added to the at least one core layer
typically exceeds the content of migrating tackifier ed to saturate the at
least one core layer with regard to the migrating tackifier. The t
required to saturate the at least one core layer may depend on the content of
polyethylene and other efins, in which the migrating tackifier is soluble,
in the at least one core layer.
According to an embodiment, the prestretched polyethylene film further
comprises an agent being selected from an additional pigment and a UV
stabilizer. An additional pigment may be advantageous for varying the color
and/or the opacity of the prestretched polyethylene film further. A UV
stabilizer may be advantageous for preventing chain reactions caused by e.g.
radicals within the polyolefin s) of the prestretched polyethylene film e.g.
during storage outdoors of the prestretched polyethylene film.
According to an embodiment, the layer prestretched polyethylene film
ses from 2 to 5 core layers. However, the etched hylene
film may comprise from 1 to up to 20 core layers.
According to an embodiment, the at least one core layer has a thickness in
the range of from 0.5 to 28 pm. In embodiments where the film comprises
multiple core layers, each core layer may have a thickness within the range of
from 0.5 pm to 28 um. Typically, the thickness of the total number of core
layers is less than 28 pm. The prestretched polyethylene film (i.e., including
all core layers and the exterior layers) may have a total thickness within the
range of from 10 to 30 pm.
The thickness values given throughout this specification refer to the thickness
of the prestretched polyethylene film or a ic layer of the prestretched
polyethylene film after the stretch film is stretched during its production (so-
called prestretching).
According to an embodiment, the prestretched polyethylene film has an
oxygen permeability of less than 10 000 cm3/m2/24 h. In particular, if the
prestretched polyethylene film serves as an agricultural film, e.g. a silage film,
good barrier ties to oxygen and other gases are important. Typically, a
silage film has an oxygen bility of less than 10 000 cm3/m2/24 h, such
as within the range of from 1000 to 10 000 cm3/m2/24 h measured according
to the rd ASTM D-1434.
According to an embodiment, the prestretched polyethylene film is an
agricultural bale wrap film or silage film.
In another aspect, the invention provides the use of a prestretched
polyethylene film as described herein. For example, the prestretched
polyethylene film may be used as an ltural film, such as a balewrap film
or a silage film. In other embodiments, the stretch film may be used as a
pallet wrapping film. In yet other embodiments, the film may be used as a
waste wrap film.
It is noted that the invention relates to all possible combinations of features
recited in the claims.
DETAILED DESCRIPTION
red embodiments of the invention will now be described in more .
The invention may, however, be embodied in many different forms and should
not be construed as limited to the embodiments set forth herein; rather, these
embodiments are provided for thoroughness and completeness, and fully
convey the scope of the invention to the skilled person.
The inventive film comprises at least 25% by weight of linear low density
polyethylene (LLDPE) substantially free from long chain branching (LCB) and
having a density below 915 kg/m3.
The film may be a single layer film or a film comprising more than one layer. A
film sing more than one layer may be called a multi-layer film.
ably, the prestretched polyethylene film according to the t
invention is a multi-layer film comprising at least three layers: at least one
core layer arranged n two exterior layers.
The prestretched polyethylene film may comprise from 1 to 5 core layers. In
embodiments, where the prestretched polyethylene film comprises more than
one core layer, the core layers may have the same composition. Alternatively,
the more than one core layers may differ in composition compared to each
other. In a preferred embodiment, the film consists of three layers; one core
layer arranged between two exterior layers.
The two exterior layers may have the same or similar composition.
Alternatively, the two or layers may differ in composition compared to
each other.
The h film may be either blown or cast. A blown stretch film has been
melted and thereafter air-cooled when blown out. A cast stretch film has been
cooled over g rollers.
The at least one core layer may form from 50% to 90%, such as from 70% to
80%, by weight of total weight of the prestretched polyethylene film. In a
etched polyethylene film comprising one core layer, the one core layer
may form from 50% to 90%, such as from 70% to 80% by weight of the total
weight of the prestretched polyethylene film. In a prestretched polyethylene
film comprising more than one core layer, the total number of core layers may
form from 50% to 90%, such as from 70% to 80%, by weight of total weight of
the prestretched polyethylene film.
The two exterior layers may together form from 10% to 50%, such as from
% to 30% by weight of the total weight of the prestretched hylene
film. Typically, the exterior layers each forms about 10% by weight of total
weight of the prestretched polyethylene film.
The prestretched polyethylene film may have a total film thickness within the
range of from 10 pm to 30 um, such as from 15 pm to 25 um, such as from 12
pm to 20 pm, for example about 19 pm. The thickness of the two exterior
layers may be within the range of from 0.5 pm to 10 um, such as from 1 pm to
pm, for example from 2 pm to 3 pm. The ess of the at least one core
layer may be within the range of from 5 to 28 um, such as from 5 pm to 25
pm, for e from 10 pm to 20 pm.
In an embodiment, the prestretched polyethylene film comprises one core
layer. The thickness of the one core layer may be within the range of from 5
to 28 um, such as from 10 pm to 25 pm, for example from 10 pm to 20 um.
Alternatively, the prestretched polyethylene film may comprise more than one
core layer. The thickness of the total number of core layers may be within the
range of from 5 to 28 um, such as from 5 pm to 25 pm, for example from 10
pm to 20 pm.
In an example, a prestretched polyethylene film comprising one core layer
and two exterior layers sandwiching the core layer may have a total film
ess of 19 pm. The core layer may have a thickness of 14 um and each
of the exterior layers has a thickness of 2.5 pm.
The prestretched polyethylene film according to the present invention
comprises at least 25% by weight of linear low density polyethylene )
substantially free from long chain branching (LCB) and having a density
below 915 kg/m3.
The portion of the prestretched polyethylene film not made up of the linear
low density polyethylene ) substantially free from long chain
branching (LCB) and having a density below 915 kg/m3 may comprise other
types of LLDPE, LDPE, and other polyolefins and ves commonly used in
the manufacture of prestretched polyethylene films. Examples of additional
polyolefin components include linear low density polyethylene (LLDPE)
having higher density, low density polyethylene (LDPE), and very low density
polyethylene (VLDPE), as well as polypropylenes and polybutylenes.
Preferably, the portion of the prestretched polyethylene film not made up of
the linear low density polyethylene ) substantially free from long chain
2016/082078
branching (LCB) and having a density below 915 kg/m3 is substantially made
up of higher density LLDPE.
In a preferred embodiment, the core layer comprises a mixture of LLDPE
substantially free from long chain branching (LCB) and having a density
below 915 kg/m3 and higher density LLDPE, wherein the LLDPE mixture has
a density below 916 kg/m3, preferably below 915 kg/m3, and more preferably
below 914 kg/m3.
The core layer and the exterior layers may have different ition. At
least one of the exterior layers may comprise a polymer such as ethylene
vinyl acetate mer (EVA) or ethylmethacrylate copolymer (EMA).
The at least one core layer may preferably comprise from 25 to 95%,
preferably from 30 to 95% or from 40 to 95% by weight of the linear low
density polyethylene (LLDPE) ntially free from long chain branching
(LCB) and having a density below 915 kg/m3, based on the total weight of the
at least one core layer. For instance, the at least one core layer comprise the
LLDPE substantially free from long chain branching (LCB) and having a
density below 915 kg/m3, at a content of from 40 to 90% by weight based on
the total weight of the core layer, such as from 40 to 70%, 40 to 60%, or 45 to
55% by weight based on the total weight of the core layer.
The prestretched hylene film according to embodiments of the invention
comprises two exterior layers. The exterior layers sandwich the at least one
core layer, i.e. the core layer is arranged between two exterior layers. By
ior layer” is meant a layer forming at least part of a surface of the film.
The exterior layers may be of identical or similar composition, or may differ in
composition. Typically however an exterior layer comprises a thermoplastic
polymer, such as a polyolefin, as a base material. es of suitable base
materials for an exterior layer include polyethylene, especially LLDPE or
VLDPE, and ne-vinyl acetate co-polymer.
WO 08891
As described herein, the prestretched polyethylene film according to the
invention ses at least two exterior layers and at least one core layer.
Typically, at least one of the two exterior layers has a certain cling. In some
embodiments, one exterior layer may have a higher degree of cling than an
exterior layer arranged on the opposite side of the core layer.
In embodiments of the invention, the prestretched hylene film may
comprise a tackifier. Typically at least one of the exterior layers may comprise
a tackifier.
Conventional tackifiers, known to the person d in the art, may be added
to the prestretched polyethylene film. Examples of conventional tackifiers
include soft polymers and migrating tackifiers. A soft polymer may provide a
relatively soft surface which may increase friction, and reduce slip in a
direction substantially el to the film surface. A migrating tackifier, on the
other hand, may provide an ve surface that increases the friction in a
direction substantially perpendicular to the film surface.
Examples of suitable soft polymers include ne vinyl acetate co-polymer
(EVA), ethyl methacrylate ymer (EMA) and very low density
polyethylene (VLDPE). Hence, in embodiments where an exterior layer
ses EVA, EMA, or VLDPE as a base material, this may provide
sufficient cling, such that it may not be necessary to add a further tackifier.
Optionally however, a layer comprising a soft polymer may also comprise a
migrating tackifier.
In an example, the cling of at least one of the exterior layers may be achieved
by the use of a soft polymer, or a combination of soft polymers, in at least one
of the two exterior layers.
VLDPE may be added to at least one exterior layer in order to provide cling to
the at least one exterior layer. In an embodiment, the content of VLDPE may
be up to 100% by weight of the at least one exterior layer. For instance, one
of the two exterior layers may consist of 100% VLDPE.
The soft polymer EVA may be used in combination with the migrating tackifier
PIB in order to provide cling to at least one exterior layer. For example, PIB
may be added to the core layer at a content that is sufficient to allow
migration to the exterior surface of at least one of the exterior layers upon
saturation of the core layer and the at least one exterior surface. EVA may be
comprised in the at least one exterior layer. An advantage of combining a soft
polymer, e.g. EVA, and a migrating tackifier, e.g. PIB, in at least one exterior
layer is that the cling may be improved due to increased resistance of the
exterior layer to forces both substantially parallel as well as substantially
perpendicular to the exterior surface of the exterior layer.
Suitable contents of at least one of a migrating tackifier, a soft r and a
combination thereof, in the at least one core layer and/or in any or both of the
two or layers of the prestretched hylene film are known to the
person skilled in the art.
A migrating tackifier may migrate within a material, including within a single
layer, as well as from one layer to an adjacent layer. In embodiments of the
present invention, a ing tackifier may e from any one of the layers
of the prestretched polyethylene film (e.g. the core layer) to the film surface of
the prestretched polyethylene film (typically the surface of an or layer).
An example of a migrating ier is polyisobutylene (PIB).
A migrating tackifier may be added to one or more layers of the prestretched
polyethylene film, typically including the thickest layer(s) of the prestretched
polyethylene film. When the prestretched polyethylene film comprises more
than one core layer, the migrating tackifier may be added to one or more,
including all, of the core layers. Alternatively, the ing ier may be
added to the thickest of the core layers. Upon saturation of the thickest
layer(s) with regard to the ing tackifier, the excess of migrating tackifier
may migrate into adjacent |ayer(s). For example, the migrating tackifier may
be initially added to the core layer, and upon saturation of the core layer, the
excess of migrating tackifier may migrate into the two exterior layers
sandwiching the core layer. Typically, also the exterior layers are saturated
with the migrating tackifier, thereby allowing the migrating tackifier to migrate
through the exterior layers and accumulate at the exterior surfaces of the
exterior layers providing cling.
The cling of at least one of the exterior layers may be achieved by addition of
a migrating tackifier to the at least one core layer. The migrating ier will
initially be comprised in the core layer, and over time migrate to the exterior
layers. The content of migrating ier added to the at least one core layer
may exceed the content of migrating tackifier required to saturate the at least
one core layer with regard to the migrating tackifier.
The migrating tackifier may be e in hylene and other polyolefins.
Thus, the content required to saturate the at least one core layer may depend
on the content of polyethylene and other polyolefins, in which the ing
tackifier is soluble, in the at least one core layer.
The at least one core layer may se migrating tackifier, e.g. in the form
of polyisobutylene (PIB), at a content of from 0 to 15% by , e.g. from 1
to 15% by weight, such as from 3 to 7% by weight, based on the total weight
of the at least one core layer. In an embodiment, the at least one core layer
comprises approximately 5% by weight of PIB.
More specifically, in an embodiment, the prestretched polyethylene film
comprises only one core layer. A migrating tackifier, e.g. in the form of PIB,
may be present in the core layer at a content of from 0 to 15% by weight, e.g.
from 1 to 15% by weight, such as from 3 to 7% by weight, based on the total
weight of the one core layer. The one core layer may se approximately
% by weight of PIB.
WO 08891
In another embodiment, the prestretched hylene film comprises more
than one core layer, such as two or more core layers arranged adjacent each
other. A migrating tackifier, e.g. PIB, may be present in one or more of the
core layers at a content of from 0 to 15% by weight, e.g. from 1 to 15% by
weight, such as from 3 to 7% by weight based on the total weight of the total
number of core layers. The core layers may together comprise approximately
% by weight of PIB. It is envisaged that when the prestretched hylene
film comprises multiple core layers, a tackifier could initially be contained in
only one of the core , or in several or all of the core layers. Typically
however, due to the nature and e of a migrating tackifier, with time all
of the layers may contain the tackifier, even if the tackifier was added only to
one of the core layers during manufacture of the multi-layer film.
By the addition of an additional pigment to the at least one core layer, the
color and the y of the prestretched polyethylene film may be further
varied. The at least one core layer may comprise an additional pigment in a
range of from 0 to 10% by weight, e.g. from 1 to 10% by weight, based on the
total weight of the at least one core layer. A prestretched polyethylene film for
silage, typically comprises from 2 to 5% by weight of an additional pigment in
the form of titanium dioxide (TiOz).
White pigments provide y by scattering visible light. An example of a
le white additional pigment is titanium dioxide (TiOz). Colored pigments
provide opacity by absorbing light. An example of a suitable d additional
pigment is carbon black (CB).
Alternatively, an additional t may be absent in the prestretched
polyethylene film. In such an embodiment, the prestretched polyethylene film
can be relatively transparent.
In some applications, a certain level of opacity may be advantageous with
regard to protection against noxious animals, such as vermin, birds, and
insects, which may harm either the prestretched polyethylene film or the
material being stored inside an arrangement of the prestretched polyethylene
film, e.g. a bale of silage. As an example, a certain level of opacity of the
prestretched polyethylene film may hinder a bird from observing the material
of the bale of silage, thereby hinder the etched polyethylene film from
being punctured by the beak or claws of the bird. The transparency of the
prestretched polyethylene film is usually within the range of from 63 to 73%,
such as approximately 70%, measured by the standard ASTM D-1003.
The prestretched hylene film according to ments of the invention
may comprise a UV stabilizer, ned in at least one layer of the multi-layer
film. Conventional UV stabilizer, known to the person skilled in the art, may be
added for example to the at least one core layer. A UV stabilizer typically
traps free radicals generated in the efin material by UV irradiation, and
may thus prevent chain ons within the efin layer(s) of the
prestretched polyethylene film, which would otherwise result in degradation of
the polyolefin material.
In embodiments of the invention, all layers of the prestretched polyethylene
film may comprise a UV stabilizer. A good UV ization of the film material
is desirable in order to avoid that the prestretched polyethylene film degrades
during storage time outdoors which typically may be up to a year.
es of suitable UV stabilizers are Chimassorb 944 (BASF, Italy),
Tinuvin 622 (BASF, Germany), and Chimassorb 2020 (BASF, ltaly). An
additional pigment, such as Ti02 or CB, may also function as a UV stabilizer.
The at least one core layer may comprise UV stabilizator in a range of from 0
to 0.6% by weight based on the total weight of the at least one core layer.
A multilayer prestretched polyethylene film according to embodiments of the
invention may be produced by a manufacturing process involving the
following steps:
a) ing a first extrudible composition sing at least 25% by
weight of linear low density polyethylene (LLDPE) substantially free
from long chain branching (LCB) and having a density below 915
kg/m3;
b) providing at least one additional extrudible composition comprising
at least one polymer;
c) extruding the first composition obtained in step a) to form at least
one core layer;
d) ing the at least one additional extrudible composition to form
two exterior layers on opposing sides of the core layer.
According to embodiments, the linear low density polyethylene (LLDPE)
substantially free from long chain branching (LCB) is produced using a Ziegler
Natta catalyst and hexene, heptene or octene as comonomer and having a
density of between 910 and 915 kg/m3.
The first extrudible composition is intended to form a core layer. The first
extrudible composition comprising comprising at least 25% by weight of linear
low density polyethylene (LLDPE) substantially free from long chain
branching (LCB) and having a density below 915 kg/m3 may be mixed with at
least one other polyolefin and ally at least one additive, e.g. selected
form the group ting of: UV stabilizers, additional pigments, and
tackifiers.
The at least one onal extrudible composition is lly intended to form
one of the exterior layers or both or layers. The step of providing at least
one additional extrudible composition comprising at least one polymer may
imply providing a second extrudible composition comprising at least one
polymer. Optionally, also a third extrudible composition comprising at least
one polymer may be provided. In particular, in embodiments where the
exterior layers have different composition, the second extrudible composition
is intended to form one of the exterior , and the third extrudible
composition is intended to form the other one of the or layers.
For example, the second extrudible composition may be provided by mixing a
soft polymer with ally at least one additive selected form the group
consisting of: UV stabilizers and iers. The second extrudible composition
is typically adapted to e cling. The third ible composition may be
provided by mixing a polyolefin, e.g. a polyethylene, with optionally at least
one additive selected form the group consisting of: UV stabilizers and
tackifiers. The third extrudible composition may be adapted to provide a low
friction surface.
Optionally, a single additional extrudible composition may be provided, which
may be adapted to provide cling and/or a low friction surface.
The step of extruding the first composition ed in step a) to form at least
one core layer may imply that the first ition is ed to a single core
layer or to multiple core layers. Typically, in the case of multiple core ,
the multiple core layers are extruded simultaneously by coextrusion and
adhere to each other due to substantially identical chemical properties.
The step of extruding the at least one additional extrudible composition to
form two exterior layers on opposing sides of the core layer may imply
extruding the second extrudible composition to form a first or layer on a
first side of the core layer and extruding the third extrudible composition to
form a second exterior layer on a second side of the core layer, wherein the
first side of the core layer is arranged opposite to the second side of the core
layen
Alternatively, the single additional extrudible composition is extruded to form
two exterior layers on opposing sides of the core layer.
The steps of extruding the first extrudible composition to form at least one
core layer and the additional extrudible composition to form two exterior
layers, respectively, may be performed separately from each other e.g. by
monoextrusion, or simultaneously e.g. by coextrusion. Typically, the
prestretched polyethylene film is prepared by co-extrusion, using one extruder
per layer simultaneously. Monoextrusion and coextrusion are techniques
generally known to the person skilled in the art.
The person skilled in the art realizes that the t invention by no means
is limited to the preferred embodiments described above. On the contrary,
many modifications and variations are possible within the scope of the
appended claims. onally, ions to the disclosed embodiments can
be understood and effected by the skilled person in practicing the claimed
invention, from a study of the drawings, the disclosure, and the appended
claims. In the claims, the word "comprising" does not exclude other elements
or steps, and the indefinite article "a" or "an" does not exclude a ity. The
mere fact that certain measures are recited in mutually ent dependent
claims does not indicate that a combination of these measured cannot be
used to advantage.
EXAMPLES
Preparatory Example 1 — Prior art balewrap (59% prestretchl
A first extrudible composition was ed. The first extrudible composition
comprised LLDPE (Dowlex 20458) with a density of 918 kg/m3 at a content of
88.5% by , Ti02 at a content of 6% by weight, a migrating tackifier in
the form of PIB (polyisobutylene) at a content of 5% by , and a UV
stabilizer at a t of 0.5% by weight based on the total weight of the first
extrudible composition.
Two additional ible compositions, namely a second extrudible
composition and a third extrudible composition, were prepared. The second
extrudible ition comprised EVA (Exxon Escorene Ultra FL 00218), at a
content of 94.5% by weight, a migrating tackifier in the form of PIB at a
content of 5% by weight, and a UV stabilizer at a content of 0.5% by weight
based on the total weight of the second extrudible composition. The third
ible composition sed polyethylene, Le. a combination of LLDPE
and LDPE, at a content of 99.5% by weight, and a UV stabilizer at a t
of 0.5% by weight based on the total weight of the third ible
composition.
The extrudible compositions were each mixed separately using blending
devices or mixing devices generally known to a person skilled in the art.
By means of coextrusion, a core layer was formed of the first extrudible
composition and two exterior layers sandwiching the core layer were formed
of the second extrudible composition and the third extrudible composition,
respectively. The coextruded film was blown and subsequently subjected to
59% prestretching. The core layer and the exterior layer together formed a
prestretched polyethylene film of a total thickness of 19 pm. The second
extrudible composition provided cling to the prestretched polyethylene film.
The third extrudible composition provided a low friction surface to the
prestretched polyethylene film.
The two exterior layers each formed 10% by weight of the total film. The core
layer formed 80% by weight of the total film.
Several tests were performed to analyze the mechanical properties of the
prestretched polyethylene film. The results of the tests are ized in
Table 1.
Preparatory Example 2 — Prior art balewrap (75% prestretch)
A first, second and third extrudible composition were prepared according to
Preparatory Example 1.
By means of usion, a core layer was formed of the first extrudible
composition and two or layers sandwiching the core layer were formed
2016/082078
of the second extrudible composition and the third extrudible composition,
respectively. The coextruded film was blown and subsequently subjected to
75% prestretching. The core layer and the exterior layer together formed a
prestretched polyethylene film of a total thickness of 19 pm. The two exterior
layers each formed 10% by weight of the total film. The core layer formed
80% by weight of the total film. Several tests were med to analyze the
mechanical ties of the prestretched polyethylene film. The results of the
tests are summarized in Table 1.
Preparatory Example 3 — Balewrap with metallocene LLDPE (75% prestretch)
A first, second and third extrudible composition were ed according to
Preparatory Example 1 with the exception that the first extrudible composition
comprised a LLDPE mixture of a metallocene LLDPE with a density of 916
kg/m3 and a melt flow index (MI2 measured at 190 °C with a 2.16 kg ) of
1.0 g/10min at a content of 48% by weight and Dowlex 20458 with a density
of 918 kg/m3 at a content of 40.5% by weight based on the total weight of the
first extrudible composition.
By means of coextrusion, a core layer was formed of the first extrudible
composition and two exterior layers sandwiching the core layer were formed
of the second extrudible composition and the third extrudible composition,
respectively. The coextruded film was blown and subsequently subjected to
75% prestretching. The core layer and the exterior layer together formed a
prestretched hylene film of a total ess of 19 pm. The two or
layers each formed 10% by weight of the total film. The core layer formed
80% by weight of the total film. Several tests were performed to analyze the
mechanical properties of the prestretched polyethylene film. The results of the
tests are summarized in Table 1.
2016/082078
Preparatory Example 4 — Balewrap with metallocene LLDPE (75% prestretch)
A first, second and third extrudible composition were prepared according to
Preparatory Example 1 with the exception that the first extrudible composition
comprised a LLDPE mixture of a metallocene LLDPE with a y of 915
kg/m3 and a melt flow index (MI2 measured at 190 °C with a 2.16 kg ) of
1.0 g/10min at a content of 48% by weight and Dowlex 20458 with a density
of 918 kg/m3 at a content of 40.5% by weight based on the total weight of the
first extrudible composition.
By means of coextrusion, a core layer was formed of the first extrudible
composition and two exterior layers sandwiching the core layer were formed
of the second extrudible composition and the third extrudible composition,
respectively. The coextruded film was blown and subsequently subjected to
75% etching. The core layer and the exterior layer together formed a
prestretched polyethylene film of a total thickness of 19 pm. The two exterior
layers each formed 10% by weight of the total film. The core layer formed
80% by weight of the total film. Several tests were med to analyze the
mechanical properties of the prestretched hylene film. The s of the
tests are summarized in Table 1.
Preparatory Example 5 — Balewrap with high melt flow index (75% prestretch)
A first, second and third extrudible composition were prepared according to
Preparatory Example 1 with the exception that the first extrudible composition
comprised a LLDPE mixture of a metallocene LLDPE with a density of 918
kg/m3 and a melt flow index (MI2 measured at 190 °C with a 2.16 kg weight) of
2.3 g/10min at a content of 48% by weight and Dowlex 20458 with a density
of 918 kg/m3 at a content of 40.5% by weight based on the total weight of the
first ible composition.
By means of coextrusion, a core layer was formed of the first extrudible
composition and two exterior layers sandwiching the core layer were formed
of the second extrudible composition and the third ible composition,
WO 08891
respectively. The coextruded film was blown and subsequently subjected to
75% prestretching. The core layer and the exterior layer together formed a
prestretched polyethylene film of a total thickness of 19 pm. The two exterior
layers each formed 10% by weight of the total film. The core layer formed
80% by weight of the total film. Several tests were performed to analyze the
mechanical properties of the prestretched polyethylene film. The results of the
tests are summarized in Table 1.
Preparatory Example 6 — Inventive ap with LLDPE substantially free
from long chain branching (LCB) and having a density below 915 kg/m3 (75%
prestretch)
A first, second and third ible composition were prepared according to
Preparatory Example 1 with the exception that the first ible composition
comprised a LLDPE mixture of an LLDPE substantially free from long chain
branching and with a density of 912 kg/m3 and a melt flow index (Ml2
measured at 190 °C with a 2.16 kg weight) of 1.0 g/10min at a content of 48%
by weight and Dowlex 20458 with a density of 918 kg/m3 at a content of
40.5% by weight based on the total weight of the first extrudible composition.
By means of coextrusion, a core layer was formed of the first extrudible
composition and two exterior layers ching the core layer were formed
of the second extrudible composition and the third extrudible composition,
respectively. The uded film was blown and subsequently subjected to
75% prestretching. The core layer and the exterior layer together formed a
prestretched hylene film of a total thickness of 19 pm. The two exterior
layers each formed 10% by weight of the total film. The core layer formed
80% by weight of the total film. Several tests were performed to analyze the
mechanical properties of the prestretched hylene film. The results of the
tests are summarized in Table 1.
Example — Comparison of ap produced according to atory
es 1-6
ap ed according to atory Examples 1-6 was subjected to
tensile testing in a tensile tester (LLOYD instruments, LR5K plus) in
accordance with the ASTM D882 standard, wherein a strip of film with a width
of 20 mm, clamped n two clamps at a distance of 50 mm from each
other is stretched at a rate of 500 mm/min until the film breaks. The results
are presented in Table 1. At five strips of the each film were measured, and
the elongation capability (elongation at break, machine direction, MD)
corresponds to the mean value of the measurements.
The stress required in order to stretch the prestretched film by 70% in the
longitudinal direction was read from the tensile strength graph obtained when
measuring the elongation percentage at break in accordance with the ASTM
D882 standard as described above. The results are presented in Table 1. At
least five strips of the film were measured, and the stress at 70% elongation
corresponds to the mean value of the measurements.
Table 1 .
Ex. 00- Ml2 Density Cat. LCB Pre— MD MD
# mon. [g/10min] [kg/m3] Stretch Stress Elong.
[%] at 70% at break
[MP8] [%]
1 Octene 1.0 918 ZN No 59% 17.5 367
2 Octene 1.0 918 ZN No 75% 19.5 298
3 Octene 1.0 916 Met. Yes 75% 21.5 289
4 Octene 1.0 915 Met. Yes 75% 22.5 263
Octene 2.3 918 ZN No 75% 19.8 331
6 Octene 1.0 912 ZN No 75% 17.7 340
Examples 1-2 represent prior art balewrap films. Examples 3-5 represent
previous attempts by the inventors to produce improved balewrap films,
resulting in films having less suitable properties. Only Example 6 resulted in a
more prestretched (75%) film having suitable tensile properties for
balewrapping.
rmore, more than 1200 bales were produced on various types of bale
wrapping machines under various wrapping conditions using the balewrap
produced ing to Preparatory Example 6. No problems with tearing of
the film were observed. Baling operators executing the bale wrapping tests
reported that the balewrap produced according to Preparatory Example 6 was
less prone to tearing or breakage even compared to the prior art film of
Example 1.
In conclusion, the inventive etched polyethylene film produced
according to Preparatory Example 6 exhibited mechanical properties that are
highly ble for use as a balewrap or silage film.
Claims (27)
1. A etched polyethylene film having a udinal degree of prestretching above 70% and a remaining longitudinal elongation capability of at 5 least 300% as determined ing to ASTM D882, wherein said film is a coextruded blown film comprising at least one core layer ed between two exterior layers, wherein the thickness of the film is in the range of 10-30 µm, and wherein the film comprises at least 25% by weight of a linear low y polyethylene (LLDPE) substantially free from long chain branching 10 (LCB) produced using a Ziegler Natta catalyst and hexene, heptene or octene as comonomer and having a density of between 910 and 915 kg/m3.
2. A prestretched polyethylene film according to claim 1, wherein the film comprises at least 35% by weight of said linear low density polyethylene 15 (LLDPE) ntially free from long chain branching (LCB).
3. A prestretched polyethylene film according to claim 2, wherein the film comprises in the range of 35-95% by weight of said linear low density polyethylene ) substantially free from long chain ing (LCB).
4. A prestretched polyethylene film according to any one of the preceding claims, wherein the linear low density polyethylene (LLDPE) substantially free from long chain branching (LCB) has a density of between 911 and 913 kg/m3.
5. A prestretched polyethylene film according to claim 3, wherein the linear low density polyethylene (LLDPE) substantially free from long chain branching (LCB) has a density of about 912 kg/m3. 30
6. A prestretched polyethylene film according to any one of the preceding claims, wherein the linear low density polyethylene (LLDPE) substantially free from long chain branching (LCB) has a melt flow index in the range of 0.7-1.3 g/10min, as determined according to ASTM D1238 (190 °C, 2.16 kg weight).
7. A prestretched polyethylene film according to claim 6, wherein the 5 linear low density polyethylene (LLDPE) substantially free from long chain branching (LCB) has a melt flow index in the range of 0.9-1.1 g/10min, as determined according to ASTM D1238 (190 °C, 2.16 kg weight).
8. A prestretched polyethylene film according to claim 6 or 7, wherein 10 the linear low density polyethylene (LLDPE) substantially free from long chain branching (LCB) has a melt flow index of about 1 n, as determined according to ASTM D1238 (190 °C, 2.16 kg weight).
9. A etched polyethylene film according to any one of the 15 preceding claims, wherein the linear low density polyethylene (LLDPE) substantially free from long chain branching (LCB) is an LLDPE ed using a Ziegler Natta catalyst and octene as mer.
10. A prestretched polyethylene film according to any one of the 20 preceding claims, said film having a udinal degree of prestretching between 70% and 100%.
11. A prestretched polyethylene film according to claim 10, said film having a longitudinal degree of prestretching between 70% and 85%.
12. A prestretched polyethylene film according to claim 10 or 11, said film having a longitudinal degree of prestretching between 71% and 79%.
13. A prestretched polyethylene film according to any one of claims 10 30 to 12, said film having a longitudinal degree of prestretching between 73% and 77%.
14. A prestretched polyethylene film according to any one of claims 10 to 13, said film having a longitudinal degree of etching about 75%.
15. A prestretched polyethylene film according to any one of the 5 preceding claims, wherein the stress required in order to stretch the prestretched film by 70% in the longitudinal direction is less than 19 MPa, as determined according to ASTM D882.
16. A prestretched polyethylene film according to claim 15, wherein the 10 stress required in order to stretch the etched film by 70% in the longitudinal direction is less than 18 MPa, as determined according to ASTM D882.
17. A prestretched polyethylene film according to any one of the 15 preceding claims, said film having a remaining longitudinal elongation capability of at least 320%, as determined ing to ASTM D882.
18. A prestretched polyethylene film ing to claim 17, said film having a remaining longitudinal elongation capability of at least 340%, as 20 determined according to ASTM D882.
19. A prestretched polyethylene film according to any one of the ing claims, wherein at least one layer comprises in the range of 40- 99% by weight of said linear low density polyethylene (LLDPE) substantially 25 free from long chain branching (LCB).
20. A prestretched polyethylene film according to any one of the preceding claims, n the at least one core layer comprises in the range of 40-99% by weight of the linear low density polyethylene (LLDPE) 30 substantially free from long chain branching (LCB).
21. A prestretched polyethylene film according to any one of the preceding claims, wherein the thickness of the film is in the range of 13-25 5
22. A prestretched polyethylene film according to any one of the ing , wherein the thickness of the film is in the range of 15-20 μm.
23. A prestretched polyethylene film according to any one of the 10 ing claims, which is an ltural balewrap film or silage film.
24. Use of a prestretched polyethylene film according to any one of the preceding claims as an agricultural balewrap film or silage film. 15
25. Use of a prestretched polyethylene film according to any one of claims 1 to 23 as a pallet wrapping film.
26. Use of a prestretched polyethylene film according to any one of claims 1 to 23 as a waste wrap film.
27. A prestretched polyethylene film according to claim 1, substantially as herein described with reference to any one of the Examples thereof.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP15201986.5A EP3184301A1 (en) | 2015-12-22 | 2015-12-22 | Prestretched balewrap |
EP15201986.5 | 2015-12-22 | ||
PCT/EP2016/082078 WO2017108891A1 (en) | 2015-12-22 | 2016-12-21 | Prestretched balewrap |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ742977A NZ742977A (en) | 2019-04-26 |
NZ742977B true NZ742977B (en) | 2019-07-30 |
Family
ID=
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