Multilayer thermoplastic film with improved puncture resistance - Patents.com

Abstract

The present disclosure provides a heat-shrinkable biaxially oriented multilayer thermoplastic film including at least a puncture-resistant layer, the puncture-resistant layer having a modulus of 0.890 g / cm as measured in accordance with ASTM D-792. 3 ~0.910g / cm 3 and a melt index (MI) of 0.20 g / 10 min to 1.5 g / 10 min as measured by ASTM D-1238 at 190°C / 2.16 kg. The polyethylene plastomer has a logM in the upper 25% of the GPC quadrant having a value of 5.1 to 5.7. 25% The multilayer thermoplastic film has a medium molecular weight distribution (Mw / Mn) of 2.5 to 3, an Mz / Mw value of 2 to 2.5, a comonomer distribution constant value of 60 to 400, a single SCBD peak between 40 and 85°C with a mass fraction above 85°C of less than 3% as determined by CEF, and a ZSVR value of 1.0 to 5.5. The multilayer thermoplastic film is biaxially stretched at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:1. [Selected Figure] Figure 1

Description

[Technical field]

[0001] The present disclosure relates generally to multilayer thermoplastic films, and more specifically to multilayer thermoplastic films having improved puncture resistance performance. [Background technology]

[0002] Food products such as poultry, fresh red meats and cheeses, as well as non-food industrial and retail goods, are packaged by a variety of heat shrink film methods. There are two main categories of heat shrink film: blown shrink film and oriented shrink film. Blown shrink film is made by a simple blown shrink film extrusion process of single bubble, while oriented shrink film is made by a more elaborate process known as double bubble, tape bubble, trapped bubble, or tenter framing. Heat shrink film can be uniaxially or biaxially oriented and is required to possess a variety of other film attributes. In addition to high shrink response, it must also possess relatively high puncture resistance for successful use in food packaging.

[0003] Shrink-wrapping techniques generally involve placing the item(s) in a bag (or sleeve) made from heat-shrinkable film, then closing or heat-sealing the bag, and then exposing the bag to sufficient heat to cause shrinkage of the bag and intimate contact between the bag and the item. Heat can be provided by conventional heat sources such as heated air, infrared radiation, hot water, combustion flame, etc. Heat-shrink packaging of food products helps preserve freshness, is attractive and sanitary, and allows for closer inspection of the quality of the packaged food. Heat-shrink packaging of industrial and retail goods, alternatively referred to in the art and herein as industrial and retail bundling, preserves product cleanliness and is also a convenient means of bundling and collating for accounting and shipping purposes.

[0004] The biaxial heat shrink response of oriented polyolefin films is obtained by first stretching the as-produced film to several times its original dimensions in both the machine and transverse directions to orient the film. Stretching is usually accomplished while the as-produced film is fully soft or molten, although cold-drawn shrink films are also known in the art. After the as-produced film is stretched, the stretch orientation is frozen or set by quenching the film while it remains in the stretched state. Subsequent application of heat can then relax the oriented film and, depending on the actual shrinkage temperature, allow the oriented film to essentially return to its original unstretched dimensions, i.e., shrink relative to its stretched dimensions.

[0005] Thus, the orientation window and shrinkage response of oriented films, which are influenced by resin properties and manufacturing parameters, are clarified. The orientation window depends on the breadth of the resin melting range, and is therefore directly related to the short-chain branching distribution of the resin. In general, ethylene alpha-olefin interpolymers with broad short-chain branching distribution and broad melting range (e.g., heterogeneously branched ultra-low density polyethylene resins such as ATTANE resins supplied by The Dow Chemical Company) show a wider orientation window compared to ethylene alpha-olefin interpolymers characterized by narrow short-chain branching distribution and narrow melting range (e.g., homogeneously branched linear ethylene polymers such as EXCEED and EXACT supplied by Exxon Chemical Corporation, and AFFINITY resins supplied by The Dow Chemical Company).

[0006] Oriented polyolefin film shrinkage depends on shrink tension and film density. Film shrinkage decreases as orientation temperature increases with lower shrink tension. Film shrinkage increases with lower density (lower crystallinity) because crystallinity provides topological constraints and therefore prevents free shrinkage. Conversely, for a given stretch ratio, shrink tension depends on the crystallinity of the resin at the orientation temperature.

[0007] The temperature at which a particular polymer is sufficiently soft or molten is an important factor in various orientation techniques, but generally, such temperatures are not defined in the art. Disclosures on oriented films that disclose various polymer types (which always have various polymer crystallinity and melting points) simply do not define the stretching or orientation temperature used in the reported comparison. U.S. Patent No. 4,863,769 to Lustig et al., WO 95 / 00333 to Eckstein et al., and WO 94 / 07954 to Garza et al. are two examples of such disclosures, the disclosures of which are incorporated herein by reference.

[0008] For example, from WO95 / 08441, the disclosure of which is incorporated herein by reference, the direct effect of density or crystallinity on shrink response and other desired shrink film properties, such as impact resistance, is known. That is, lower density polymer films exhibit higher shrink response and improved impact resistance, even if the orientation temperature is supposedly constant. However, the effect of density and other resin properties on orientation temperature is not well known. In the prior art, there are only general rules of thumb or generalized teachings related to suitable stretching or orientation conditions. For example, in commercial operations, it is often said that the temperature at which a film is adequately soft or melted is just above the respective glass transition temperature for amorphous polymers, or below the respective melting point for semi-crystalline polymers. Multilayer structures composed of different polymers can further expand these ranges, allowing stretching to occur above the melting points of some components and below others.

[0009] Although the effect of density and other resin properties on the optimum orientation temperature of polyolefins is generally not known, it is clear that heterogeneously branched ethylene polymers such as ATTANE™ resins and DOWLEX™ resins have a relatively wide orientation window (i.e., the temperature range over which the resin can be substantially stretched when melted or softened). It is also clear that the softening temperature and other film properties, such as secant modulus, tend to decrease at lower polymer densities. Because of these relationships, films with high shrink response, wide orientation window, high puncture resistance, high modulus and high softening temperature (i.e., shrink films with balanced properties) are not known in the prior art. That is, polymer designers must always sacrifice orientation window to provide films with puncture resistance and high modulus. The importance of a higher modulus is related to the need for, for example, good machinability during automated packaging operations and good handling during bag making operations.

[0010] An example of a teaching beyond the general rule of thumb (but rather generalized) is provided by Golike in U.S. Pat. No. 4,597,920, the disclosure of which is incorporated herein by reference. Golike uses at least one C8-C 18Golike teaches that orientation should be performed at a temperature between the lower and higher melting points of the copolymer of ethylene with an α-olefin. Golike specifically teaches that the temperature difference is at least 10° C., however, Golike also specifically discloses that the full range of temperature difference may not be practical since tearing of the polymer film may occur at the lower end of the range depending on the particular equipment and technology used. At the higher end of the range, Golike teaches that the structural integrity of the polymer film begins to degrade during stretching (and ultimately breaks down at higher temperatures) since the polymer film is then in a soft, molten state. See U.S. Pat. No. 4,597,920, column 4, lines 52-68 to column 5, lines 1-6. The orientation temperature range defined by Golike (based on the higher and lower peak melting points) generally applies to polymer blends and heterogeneously branched ethylene / α-olefin interpolymers, i.e., compositions with two or more DSC melting points, and does not apply at all to homogeneously branched ethylene / α-olefin interpolymers with only a single DSC melting point. Golike also indicates that one skilled in the art can determine the tear temperature of a particular polymer, which is about 0.920 g / cm 3 Golike discloses that for heterogeneously branched interpolymers having a density of 0.1 to 0.5 mm, the tear temperature occurs above the lower peak melting point. See U.S. Pat. No. 4,597,920, column 7, example 4. However, Golike does not teach or suggest how one skilled in the art of shrink film can optimize the orientation process for a given stretching speed and ratio and stretching temperature to maximize the shrink response and achieve balanced properties.

[0011] Hideo et al., EP 0359907 A2, the disclosure of which is incorporated herein by reference, teaches that the film surface temperature at the start of stretching should be within 20°C to about 30°C below the melting temperature of the polymer as determined by the DSC main endothermic peak. Such teachings are believed to be applicable to homogeneously branched ethylene / α-olefin interpolymers having a single DSC melting peak, but the ranges specified are fairly general and broad. Furthermore, Hideo et al. do not provide any specific teachings regarding the optimum orientation temperature of a particular interpolymer for heat shrink response, or any other desired shrink film properties.

[0012] WO 95 / 08441, the disclosure of which is incorporated herein by reference, provides generalized teachings regarding homogeneously branched ethylene / cc-olefin interpolymers. In the examples of this disclosure, several different homogeneously branched substantially linear ethylene / α-olefin interpolymers were studied and compared to one heterogeneously branched ethylene / α-olefin interpolymer. The homogeneously branched substantially linear ethylene / α-olefin interpolymers had a molecular weight of about 0.896 to about 0.906 g / cm. 3 Although the densities varied, all interpolymers (0.905 g / cm 3Heterogeneously branched linear ethylene / α-olefin interpolymers (including ATTANE® 4203, supplied by The Dow Chemical Company, having a density of 1000 nm to 1000 nm) were oriented at essentially the same orientation temperature. The results reported in WO95 / 08441 disclose three general findings: (1) at comparable polymer densities, substantially linear ethylene / α-olefin interpolymers and heterogeneously branched linear ethylene / cc-olefin interpolymers have essentially equivalent shrinkage response (compare Examples 21 and 39, pages 15-16), (2) shrinkage response increases at lower density and constant orientation temperature, and (3) orientation rate increases as orientation temperature increases. Furthermore, careful study of the interpolymer examples reported in WO95 / 08441 and unreported DSC melting point data for the examples disclosed in WO95 / 08441 indicates that for a given stretch rate and ratio, it is preferable to orient the multilayer film structure at an orientation temperature above the respective DSC melting points of the polymers used as shrink control layers. Furthermore, none of the teachings or examples in WO95 / 08441 suggest that a shrink film having balanced properties can be obtained.

[0013] Other disclosures which describe orientation information for homogeneously branched ethylene polymers but do not specify orientation conditions for respective minimum stretch temperatures and do not teach requirements for balanced shrink film properties include EP 0600425 A1 to Babrowicz et al. and EP 0587502 A2 to Babrowicz et al., the disclosures of which are incorporated herein by reference.

[0014] Thus, while there are general rules and general disclosures regarding shrink response and suitable orientation temperatures for biaxially oriented polyolefins, there is no specific information regarding optimal orientation conditions as a function of polymer type, and more importantly, there is no specific information regarding balanced or optimized shrink response, wide orientation window, high modulus, and / or high puncture resistance. It is therefore an object of the present disclosure to provide improved shrink films with maximized shrink response, increased orientation window, and relatively high puncture resistance for a given modulus or polymer density. This and other objects will become apparent from the description and various following. Summary of the Invention

[0015] The present disclosure provides a hardness of 0.890 g / cm as measured in accordance with ASTM D-792. 3 ~0.910g / cm 3 and a melt index (MI) of 0.20 g / 10 min to 1.5 g / 10 min as measured at 190° C. / 2.16 kg by ASTM D-1238. The polyethylene-based plastomer has a logM 25% , intermediate molecular weight distribution (Mw / Mn) of 2.5-3, Mz / Mw value of 2-2.5. The polyethylene-based plastomer is further characterized by a single SCBD peak at 40-85°C with a comonomer distribution constant value of 60-400 and a mass fraction above 85°C of less than 3% and a ZSVR value of 1.0-5.5 as determined by CEF. The multilayer thermoplastic film is biaxially stretched at temperatures between 60°C and 120°C with a blow-up ratio of 2:1 to 10:1. The polyethylene-based plastomer can also have an MI of 0.75 g / 10 min to 1 g / 10 min as measured at 190°C / 2.16 kg by ASTM D-1238. The polyethylene-based plastomer can have a MI of 0.900 g / cm2 as determined according to ASTM D-792. 3 ~0.910g / cm 3The density of the powder may be 0.01 to 0.01.

[0016] In one embodiment, the polyethylene-based plastomer of the puncture resistant layer is an ethylene interpolymer having at least one α-olefin of 3 to 20 carbon atoms. In an alternative embodiment, the polyethylene-based plastomer of the puncture resistant layer is an ethylene / α-olefin copolymer. In one embodiment, the ethylene / α-olefin copolymer is an ethylene / 1-octene copolymer. The puncture resistant layer can further comprise 5 weight percent to 50 weight percent of an ethylene / vinyl acetate copolymer based on the weight of the blend. Alternatively, the polyethylene-based plastomer of the puncture resistant layer is mixed with 5 weight percent to 50 weight percent of a heterogeneously branched ultra-low density polyethylene or a heterogeneously branched very-low density polyethylene or a heterogeneously branched linear low density polyethylene based on the weight of the blend.

[0017] For various embodiments, the multilayer thermoplastic film may further include a second polymer layer adjacent to the puncture resistant layer, and the puncture resistant layer and the second polymer layer of the multilayer thermoplastic film are biaxially stretched at a blow-up ratio of 2:1 to 10:1 at a temperature of 60° C. to 120° C. For various embodiments, the second polymer layer may be formed from a polymer selected from the group consisting of ultra-low density polyethylene, very-low density polyethylene, ethylene / α-olefin interpolymers, ethylene / α-olefin block copolymers, ethylene-vinyl acetate copolymers, polyamides, copolymers of polyvinylidene chloride, ethylene vinyl alcohol, or linear low density polyethylene grafted maleic anhydride. In addition, the multilayer thermoplastic film may also further include a third polymer layer disposed between the puncture resistant layer and the second polymer layer, and the puncture resistant layer, the second polymer layer and the third polymer layer of the multilayer thermoplastic film are biaxially stretched at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:1. The second polymer layer and the third polymer layer are independently formed from a polymer selected from the group consisting of ultra-low density polyethylene, very-low density polyethylene, ethylene / α-olefin interpolymer, ethylene / α-olefin block copolymer, ethylene-vinyl acetate copolymer, polyamide, copolymer of polyvinylidene chloride, ethylene vinyl alcohol or linear low density polyethylene grafted maleic anhydride. In one embodiment, the polymer of the second polymer layer is structurally different from the polymer of the third polymer layer. For various embodiments, the third polymer layer is an ethylene-vinyl acetate copolymer and the second polymer layer includes an ethylene / α-olefin interpolymer and an ultra-low density polyethylene.

[0018] The biaxially oriented polymer film of the present disclosure can also include a barrier polymer layer and a tie layer adjacent to the puncture resistant layer or second layer, where the puncture resistant layer and the set of barrier and tie layers of the biaxially oriented polymer film are biaxially stretched at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:1.

[0019] For the embodiments provided herein, the multilayer thermoplastic film can be prepared by a double bubble process. The multilayer thermoplastic film is suitable for use in packaging food items.

[0020] The present disclosure also provides a method for forming a heat shrinkable biaxially oriented multilayer thermoplastic film suitable for use in the manufacture of bags for packaging food items. The method has a yield of 0.890 g / cm as determined in accordance with ASTM D-792. 3 ~0.910g / cm 3 and a melt index (MI) of 0.20 g / 10 min to 1.5 g / 10 min as measured by ASTM D-1238, condition 190° C. / 2.16 kg, wherein the polyethylene plastomer has a logM 25%forming a first multi-layer structure having a medium molecular weight distribution (Mw / Mn) of 2.5-3 and a Mz / Mw value of 2-2.5, a single SCBD peak at 40-85°C with a distribution constant value of 60-400 and a mass fraction above 85°C of less than 3% as determined by CEF, and a ZSVR value of 1.0-5.5; collapsing the first extrusion bubbles to form a first multi-layer structure; passing the first multi-layer structure through a first water bath having a temperature of 5°C-50°C to cool the first multi-layer structure, wherein the first multi-layer structure has a residence time in the water of the first water bath of 0.5-50 seconds; warming the first multi-layer structure coming from the first water bath by passing the first multi-layer structure through a second water bath having a temperature of 80°C to 100°C, the first multi-layer structure having a residence time in the water of the second water bath of 5 to 50 seconds; heating the first multi-layer structure to a temperature of 60°C to 120°C; forming a second extrusion bubble while the first multi-layer structure is heated to a temperature of 60°C to 120°C, the first structure having a blow-up ratio of 2:1 to 10:1 when forming the second extrusion bubble; and collapsing the second extrusion bubble to form a heat shrinkable biaxially oriented multi-layer thermoplastic film. [Brief description of the drawings]

[0021] [Figure 1] An apparatus for preparing multi-layer structures using the double bubble or trapped bubble process. [Diagram 2] 1 is a graph of gel permeation chromatography results for the intermediate molecular weight distribution of Affinity™ PL 1880G, Affinity™ PL 1860G and Attane™ 4203G. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0022] The present disclosure provides a heat shrinkable biaxially oriented multilayer thermoplastic film, a method for making the same, and articles made therefrom. The heat shrinkable biaxially oriented multilayer thermoplastic film of the present disclosure has a hardness of 0.890 g / cm 3 ~0.910g / cm 3and a melt index (MI) measured at 190°C / 2.16kg of 0.2g / 10min to 1.5g / 10min. The polyethylene-based plastomer has a logM 25% , intermediate molecular weight distribution (Mw / Mn) of 2.5-3 and Mz / Mw value of 2-2.5. The composition is further characterized by a single SCBD peak between 40-85°C with a comonomer distribution constant value of 60-400 and a mass fraction above 85°C of less than 3% as determined by CEF, and a ZSVR value of 1.0-5.5. The multilayer thermoplastic films of the present disclosure are biaxially stretched at temperatures between 60°C and 120°C with a blow-up ratio of 2:1 to 10:1.

[0023] For various embodiments, the polyethylene-based plastomers of the present disclosure have a modulus of 0.890 g / cm 3 ~0.910g / cm 3 Preferably, the polyethylene-based plastomer of the present disclosure has a density of 0.900 g / cm 3 ~0.910g / cm 3 The densities provided herein are determined in accordance with ASTM D-792.

[0024] The melt index of a polymer is inversely proportional to the molecular weight of the polymer. Thus, the higher the molecular weight, the lower the melt index, although the relationship is not linear. For various embodiments, the polyethylene-based plastomers of the present disclosure have a melt index (MI) measured at 190°C / 2.16kg (I2) of 0.2g / 10min to 1.5g / 10min. Preferably, the polyethylene-based plastomers of the present disclosure have a MI measured at 190°C / 2.16kg (I2) of 0.50g / 10min to 1.5g / 10min. More preferably, the polyethylene-based plastomers of the present disclosure have a MI measured at 190°C / 2.16kg (I2) of 0.75g / 10min to 1.5g / 10min. The MI value measured at 190°C / 2.16kg is determined according to ASTM D-1238.

[0025] Other measurements useful for characterizing the molecular weight of the polyethylene-based plastomers of the present disclosure are, for example, conventional ASTM D-1238, condition 190° C. / 10 kg (I 10 The ratio of the higher weight melt index determination to the lower weight determination is known as the melt flow ratio and is the measured I 10 For I2 melt index values, the melt flow ratio is conveniently expressed as I 10 For the polyethylene-based plastomers of the present disclosure used to prepare the puncture resistant layer of the heat shrinkable biaxially oriented multilayer thermoplastic film of the present disclosure, the melt flow ratio depends on the molecular weight distribution and / or the degree of long chain branching, i.e., I 10 A higher I2 melt flow ratio indicates a broader MWD in the polymer and / or longer chain branching in the polymer. In addition to indicating MWD and long chain branching, a higher I 10 The / I2 ratio also indicates lower viscosity at higher shear rates (easier processing) and higher elongational viscosity. 10 The / I2 ratio is preferably in the range of 6 to about 15. More preferably, the I / I2 ratio of the polyethylene plastomer of the present disclosure is 10 The / I2 ratio is in the range of about 7 to about 12 or about 8 to 10.

[0026] For various embodiments, the polyethylene-based plastomer has a logM 25% Preferably, the polyethylene plastomer has a logM 25% The logM in the upper 25% of the GPC quadrants 25%is calculated using the quadrants from the MWD using GPC. Calculation of the quadrants from the MWD by GPC is as follows: The plotted molecular weight distribution from GPC (dWf / dLogM vs. LogM) has, by definition, an area equal to 1. The plot is divided into four equivalent area sections (weight fraction = 0.25) integrated from high molecular weight to low molecular weight. For each quadrant, the average logM was determined (25%, 50%, 75%, 100%) as follows: Equations 1A-1D:

number

number

number

number

[0027] Here, the MWD region is integrated from the highest detectable logMw to the lowest detectable logMw at each dWf / dLogM, and each slice (i) represents 0.01 LogMw in width. The average GPC molecular weight for each quadrant is calculated as follows: 10^LogM 象限 And this value differs from the mathematical mean obtained by taking the average of 10^LogMi at each slice (i) in the quadrant.

[0028] The puncture resistant layer of the multilayer thermoplastic film of the present disclosure has a molecular weight distribution (M w / M n The number average molecular weight (M n The weight average molecular weight (M) value is determined from the molecular weight value of a polyethylene-based plastomer measured using gel permeation chromatography with a differential refractive index detector, using polystyrene of known molecular weight as a standard, as known in the art.w The value of ) is determined from known techniques such as static light scattering, small angle neutron scattering, X-ray scattering or sedimentation velocity.

[0029] Methods for measuring Mz are found in the conventional gel permeation chromatography description in the Examples section of this disclosure. The puncture resistant layer of the multilayer thermoplastic film of the present disclosure further comprises a molecular weight distribution (Mz / Mw) of 2 to 2.5. w ) is determined as discussed above.

[0030] In one embodiment, the polyethylene-based plastomer of the puncture resistant layer is a polyethylene-based plastomer having 3 to 20 carbon atoms (C 20 Polyethylene-based plastomers suitable for use in the puncture resistant layer include substantially linear ethylene interpolymers, homogeneously branched linear ethylene interpolymers, heterogeneously branched linear ethylene interpolymers (e.g., linear low density polyethylene (LLDPE), and ultra-low or very-low density polyethylene (ULDPE or VLDPE)), and combinations or mixtures thereof.

[0031] Examples of polyethylene-based plastomers for the puncture resistant layer of the present disclosure include those provided in U.S. Patent No. 8,389,086 B2, which is incorporated herein by reference in its entirety. For various embodiments, the polyethylene-based plastomer has a melt index of less than 2 grams / 10 minutes, or alternatively, a melt index of 0.2 to 1.5 grams / 10 minutes, a viscosity of 0.910 g / cm 3 For example, 0.8602 to 0.910 g / cm 3The polyethylene-based plastomer may have a density of at least 2.5, a total heat of fusion of less than 120 Joules / gram, and a heat of fusion of greater than 115°C of less than 5 Joules / gram. In addition, the polyethylene-based plastomer may have a molecular weight distribution (Mw / Mn) of at least 2.5, e.g., 2.5 to 3.5, and a comonomer distribution constant (CDC) of greater than about 45 and up to 400. The polyethylene-based plastomer may have a CDC of 60 to 400 in some embodiments, or 100 to 300 in some other embodiments, or 100 to 200 in some other embodiments. The polyethylene-based plastomer may also have less than 120 total unsaturated units / 1,000,000 carbons (C). The CDC is defined as the comonomer distribution index divided by the comonomer distribution shape factor times 100. The comonomer distribution index is the ratio of the comonomer content to the median comonomer content (C 中央値 ) of 0.5 and C 中央値 represents the total weight fraction of polymer chains in the range of 35.0-119.0°C. The comonomer distribution shape factor is defined as the ratio of the width at half-height (half-width) of the comonomer distribution profile divided by the standard deviation (Stdev) of the comonomer distribution profile from the peak temperature (Tp). The polyethylene-based plastomers can also have any combination of the following properties in addition to those provided above: up to about 3 long chain branches / 1000 carbons; less than 20 vinylidene unsaturated units / 1,000,000C; a single DSC melting peak. In one embodiment, the polyethylene-based polymers that can be used in the puncture resistant layer have the following CDC and CDI values: [Table 1]

[0032] Preferably, a single-site catalyst system is used to manufacture the polyethylene-based plastomer of the puncture resistant layer, and depending on the process conditions, a certain level of long chain branching (LCB) is found in the system. Preferably, the level of LCB in the polyethylene-based plastomer is measured by calculating the zero shear viscosity ratio (ZSVR). ZSVR is defined as the ratio of the zero shear viscosity (ZSV) of a branched polyethylene material to the ZSV of a linear polyethylene material at an equivalent weight average molecular weight according to the formula:

number

[0033] ZSV values ​​were obtained from creep tests at 190°C by the method described above. Mwt is determined using gel permeation chromatography as described above. A correlation between the ZSV of a linear polyethylene and its molecular weight was established based on a series of linear polyethylene reference samples. A lower ZSVR indicates a lower level of long chain branching. Preferred ZSVR values ​​for the polyethylene-based plastomers of the puncture resistant layer are values ​​between 1.0 and 5.5, preferably between 2.5 and 5.5, more preferably between 2.5 and 3.5 or between 4.5 and 5.5. Substantially linear ethylene polymers are sold under the names AFFINITY™ and ENGAGE™ resins by The Dow Chemical Company and Dupont Dow Elastomers, respectively. Uniformly branched linear ethylene polymers are sold under the names TAFMER™ by Mitsui Chemical Corporation and EXACT™ and EXCEED™ resins by Exxon Chemical Corporation, respectively. Heterogeneously branched linear ethylene polymers are sold by The Dow Chemical Company under the names ATTANE™, DOWLEX™ and FLEXOMER.

[0034] The term "substantially linear ethylene polymer" as used herein refers to a homogeneously branched ethylene / α-olefin interpolymer having a narrow short-chain branching distribution and containing long-chain branching as well as short-chain branching resulting from homogeneous comonomer incorporation. Typically, the polyethylene-based plastomer of the puncture-resistant layer is an ethylene / α-olefin copolymer (e.g., a homogeneously branched substantially linear ethylene polymer or a homogeneously branched linear ethylene polymer). It may also be a blend of two or more homogeneously branched substantially linear ethylene polymers or homogeneously branched linear ethylene polymers. The blend of two or more homogeneously branched substantially linear ethylene polymers or homogeneously branched linear ethylene polymers may be a blend formed in situ in a reactor, the polymers having approximately the same density but different molecular weights.

[0035] The α-olefin of the ethylene / α-olefin copolymer is at least one C3-C6 olefin such as propylene, isobutylene, 1-butene, 1-hexene, 4-methyl-1-pentene, 1-heptene, 1-octene, 1-nonene, and 1-decene. 20 The α-olefins are preferably propylene, 1-butene, 1-hexene, 4-methyl-1-pentene, and 1-octene, with 1-octene being particularly preferred. Most preferably, the ethylene / α-olefin interpolymers are made of ethylene and C3-C 20 α-Olefin copolymers, especially ethylene / C4-C 10 α-olefin copolymers and most particularly ethylene / 1-octene copolymers. Other suitable monomers include styrene, halo- or alkyl-substituted styrenes, tetrafluoroethylene, vinylbenzocyclobutane, 1,4-hexadiene, 1,7-octadiene, and cycloalkenes such as cyclopentene, cyclohexene, and cyclooctene.

[0036] Long chain branches are of the same structure as the polymer backbone and are longer than the short chain branches. Substantially linear polymer backbone (α-olefin polymers substituted with an average of 0.01 to 3 long chain branches / 1000 carbons). Preferred substantially linear polymers for use in the present disclosure are substituted with 0.01 long chain branches / 1000 carbons to 1 long chain branch / 1000 carbons, more preferably 0.05 long chain branches / 1000 carbons to 1 long chain branch / 1000 carbons.

[0037] Long chain branching is defined herein as a chain length of at least 6 carbons, beyond which 13 C nuclear magnetic resonance spectroscopy. A long chain branch can be as long as the polymer backbone to which it is attached. It is obviously longer in length than the short chain branches resulting from comonomer incorporation.

[0038] The presence of long chain branches in ethylene homopolymers is 13 It can be measured using C nuclear magnetic resonance (NMR) spectroscopy and quantified using the method described in Randall (Rev. Macromol. Chem. Phys., C29, V.2&3, p.285-297). Other known techniques useful for determining the presence of long chain branching in ethylene polymers, including ethylene / 1-octene interpolymers. Two such methods are gel permeation chromatography coupled with a low angle laser light scattering detector (GPC-LALLS) and gel permeation chromatography coupled with a differential viscometer detector (GPC-DV).

[0039] The term "homogeneously branched linear ethylene polymer" is used in the conventional sense with respect to linear or substantially linear ethylene interpolymers in which the comonomer is randomly distributed within a given polymer molecule and substantially all of the polymer molecules have the same molar ratio of ethylene to comonomer. The term refers to an ethylene interpolymer characterized by a relatively high short chain branching index (SCBDI) or composition branching index (CDBI). That is, the interpolymer has an SCBDI of about 50% or more, preferably about 70% or more, more preferably about 90% or more, and is essentially devoid of measurable high density (crystalline) polymerizable moieties in a TREF analysis.

[0040] The SCBDI of interpolymers is described, for example, in Wild et al., Journal of Polymer Science, Poly.Phys.Ed., Vol.20, p.441 (1982), or U.S. Patent Nos. 4,798,081 and 5,008,204, or LD Cady, "The Role of Comonomer Type and Distribution in LLDPE Product Performance", SPE Regional Technical Conference, Quaker Square Hilton, Akron, Ohio, October 1-2, pp.107-119 (1985), the disclosures of which are all incorporated herein by reference. However, the preferred TREF technique does not include the purge amount in the SCBDI calculation. More preferably, the monomer distribution of the interpolymers and SCBDI is determined using 13 C NMR according to the techniques described in U.S. Pat. No. 5,292,845 and JC Randal, Rev. Macromol. Chem. Phys., C29, pp. 201-317, the disclosures of both of which are incorporated herein by reference.

[0041] In addition to referring to a uniform (or narrow) short branch distribution, the term "uniformly branched linear ethylene interpolymer" also means that the interpolymer has no long chain branching or substantially linear ethylene interpolymer. That is, the ethylene interpolymer has an absence of long chain branching and linear polymer backbone in the conventional sense of the term "linear". However, the term "uniformly branched linear ethylene polymer" does not refer to high pressure branched polyethylene, which is known to those skilled in the art to have a large number of long chain branches. A polymerization process that provides a uniform (narrow) short branch distribution (i.e., uniformly branched) (e.g., those described by Elston in U.S. Pat. No. 3,645,992) can be used to make the uniformly branched ethylene polymer. The uniformly branched linear ethylene polymer can be prepared in a solution, slurry, or gas phase process using hafnium, zirconium, and vanadium catalyst systems.

[0042] That is, the interpolymers have a relatively broad short chain branching distribution. Heterogeneously branched linear ethylene polymers have an SCBDI of less than about 50%, more typically less than about 30%.

[0043] Heterogeneously branched ethylene polymers are well known among practitioners of linear polyethylene technology. Heterogeneously branched ethylene polymers are prepared using conventional Ziegler-Natta solution, slurry or gas phase polymerization processes and coordination metal catalysts. These conventional Ziegler-Natta type linear polyethylenes are not uniformly branched, do not have any long chain branching, and therefore have a linear polymer backbone in the conventional sense of the term "linear."

[0044] The puncture resistant layer may further comprise 5 to 50 weight percent of an ethylene / vinyl acetate copolymer based on the weight of the blend. Alternatively, the polyethylene-based plastomer of the puncture resistant layer is blended with 5 to 50 weight percent of a heterogeneously branched ultra-low density polyethylene or a heterogeneously branched very-low density polyethylene based on the weight of the blend. Blends and mixtures of the polyethylene-based plastomer of the puncture resistant layer composition with other polyolefins may also be practiced. Suitable polymers for blending with the polyethylene-based plastomer of the puncture resistant layer composition include thermoplastic and non-thermoplastic polymers, including natural and synthetic polymers. Exemplary polymers for blends include various types of polyethylene including polypropylene (both impact modified polypropylene, isotactic polypropylene, atactic polypropylene, random ethylene / propylene copolymers and random ethylene / propylene / butene terpolymers), high pressure, free radical LDPE, Ziegler-Natta LLDPE, metallocene PE, multiple reactor PE ("in reactor" blends of Ziegler-Natta PE and metallocene PE), homogeneous polymers such as ethylene-vinyl acetate (EVA), ethylene / vinyl alcohol copolymers, olefin plastomers and elastomers, ethylene and propylene based copolymers (e.g., polymers available under the tradenames VERSIFY™ plastomers and elastomers (The Dow Chemical Company), SURPASS™ (Nova Chemicals), and VISTAMAXX™ (ExxonMobil Chemical Co.) may also be useful in blends with polyethylene based plastomers of the puncture resistant layer composition.

[0045] The multilayer thermoplastic film of the present disclosure may have a pre-shrink thickness of 10 micrometers (μm) to 200 μm. Preferably, the multilayer thermoplastic film has a thickness of 30 μm to 100 μm. As discussed herein, the polyethylene-based plastomer of the multilayer thermoplastic film has a thickness of 3 μm to 90 μm.

[0046] Although the puncture-resistant layer discussed herein can be used as a single layer, the multilayer thermoplastic film of the present disclosure can also be one or more additional layers. For example, the multilayer thermoplastic film can further include a second polymer layer adjacent to the puncture-resistant layer, and the puncture-resistant layer and the second polymer layer of the multilayer thermoplastic film are biaxially stretched at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:1. In addition, the multilayer thermoplastic film can also further include a third polymer layer disposed between the puncture-resistant layer and the second polymer layer, and the puncture-resistant layer, the second polymer layer and the third polymer layer of the multilayer thermoplastic film are biaxially stretched at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:1. The second and third polymer layers are independently formed from a polymer selected from the group consisting of ultra-low density polyethylene, very-low density polyethylene, ethylene / α-olefin interpolymer, ethylene / α-olefin block copolymer, ethylene-vinyl acetate copolymer, polyamide, copolymer of polyvinylidene chloride, ethylene vinyl alcohol or linear low density polyethylene grafted maleic anhydride. In one embodiment, the polymer of the second polymer layer is structurally different from the polymer of the third polymer layer. For various embodiments, the third polymer layer is an ethylene-vinyl acetate copolymer and the second polymer layer comprises an ethylene / α-olefin interpolymer and an ultra-low density polyethylene. These additional layers and their functions in the multilayer thermoplastic film are discussed more fully herein.

[0047] For various embodiments, the multilayer thermoplastic film of the present disclosure includes at least two additional layers, with the puncture resistant layer formed of a polyethylene-based plastomer polyethylene providing an inner layer of the multilayer thermoplastic film (e.g., disposed between the at least two additional layers).Thus, it is preferred that the puncture resistant layer be used in a multilayer thermoplastic film having three or more layers, more preferably between three and nine layers, and even more preferably between three and five or between three and seven layers.

[0048] In the case of coextruded or laminated multilayer film structures (e.g., three-layer film structures), the puncture-resistant layers described herein can be used as the core layer, the outer surface layer, the middle layer, and / or the inner sealant layer of the structure. Generally, for multilayer film structures, the puncture-resistant layer comprises at least 10% of the total multilayer film structure. Other layers of the multilayer structure include, but are not limited to, barrier layers, and / or tie layers, and / or structural layers. A variety of materials can be used for these layers, some of which are used as multiple layers in the same film structure. Some of these materials include foil, nylon, ethylene / vinyl alcohol (EVOH) copolymers, polyvinylidene chloride (PVDC), polyethylene terephthalate (PET), oriented polypropylene (OPP), ethylene / vinyl acetate (EVA) copolymers, ethylene / acrylic acid (EAA) copolymers, ethylene / methacrylic acid (EMAA) copolymers, ULDPE, LLDPE, HDPE, MDPE, LMDPE, LDPE, ionomers, graft modified polymers (e.g., maleic anhydride grafted polyethylene), and paper.

[0049] Thus, the heat shrinkable biaxially oriented multilayer thermoplastic film with a puncture resistant layer of the present disclosure may be a 2-15 layer structure having a core layer formed from a sealant layer composition (such as, but not limited to, another polymer blend, at least one homogeneously branched substantially linear ethylene polymer, at least one homogeneously branched linear ethylene polymer, or at least one heterogeneously branched ultra or very low density polyethylene), an outer layer (such as, but not limited to, another polymer blend or at least one heterogeneously branched linear low density or ultra-low density polyethylene), and a puncture resistant layer as provided herein. Adhesion promoting tie layers (such as PRIMACOR™ ethylene-acrylic acid (EAA) copolymers, MAH-grafted ethylene copolymers (MAH PE), and / or ethylene-vinyl acetate (EVA) copolymers available from SK Chemical) may optionally be used, as well as additional structural layers such as Affinity™ polyolefin plastomers, Engage™ polyolefin elastomers (both available from The Dow Chemical Company), ultra-low density polyethylene, or blends of any of these polymers with each other or with another polymer such as EVA.

[0050] Other layers of the multi-layer structure include, but are not limited to, barrier layers, and / or tie layers, and / or structural layers, as discussed herein. A variety of materials can be used for these layers, some of which are used as multiple layers in the same film structure. Some of these materials include nylon, ethylene / vinyl alcohol (EVOH) copolymers, polyvinylidene chloride (PVDC), polyethylene terephthalate (PET), ethylene / vinyl acetate (EVA) copolymers, ethylene / acrylic acid (EAA) copolymers, ethylene / methacrylic acid (EMAA) copolymers, ULDPE, LLDPE, HDPE, MDPE, LMDPE, LDPE, ionomers, graft modified polymers (e.g., maleic anhydride grafted polyethylene).

[0051] Examples of possible multi-layer constructions include: a puncture resistant layer of the present disclosure / MAH PE(tie) / EVOH / MAH PE(tie) / PE; a puncture resistant layer of the present disclosure / EVA of the present disclosure / puncture resistant layer / EVA / heat sealing layer; or a puncture resistant layer of the present disclosure / EVA / PVDC / EVA / outer layer (wherein the outer layer is selected from a plastomer or other ethylene alpha olefin interpolymer sealant provided herein, PE (e.g., LLDPE or ULDPE), EVA, PVDC, EVA or a sealant layer).

[0052] In one embodiment disclosed herein, a multilayer film structure includes at least three layers (e.g., an "A / B / A" structure), where at least one core or hidden layer is a puncture-resistant layer, as discussed herein. In general, the ratio of film structure layers is such that the core layer dominates the film structure in terms of its overall structure percentage. In one embodiment, the multilayer thermoplastic film of the present disclosure provides a puncture-resistant layer formed with a polyethylene-based plastomer polyethylene having two outer layers, the puncture-resistant layer comprising 10 weight percent (wt%) to 90 wt% of the multilayer thermoplastic film based on the total weight of the multilayer thermoplastic film. For example, the core layer can be at least about 33 wt% of the total film structure (e.g., in a three-layer film structure, each "A" outer layer comprises 33 wt% of the total film structure, and the core puncture-resistant layer ("B" layer) comprises 33 wt% of the total film structure). In a three-layer film structure, preferably, the core puncture-resistant layer comprises at least about 70% of the total film structure. Additional hidden layers may also be incorporated into the film structure without compromising the optical properties. For example, tie or intermediate layers may be used, including, for example, ethylene / vinyl acetate copolymer, ethylene acrylamide copolymer, or anhydride-grafted modified polyethylene, or barrier layers may be used, including, for example, vinylidene chloride / vinyl chloride copolymer or ethylene vinyl alcohol copolymer. In a more preferred three-layer film structure, each "A" outer layer comprises 15% by weight of the total film structure of at least one substantially linear ethylene polymer, and the "B" puncture-resistant layer comprises 70% by weight of the total film structure. The multilayer film structure may be oriented and / or irradiated (in any order) to provide a multilayer shrink film structure with improved puncture resistance.

[0053] For the various embodiments, at least one of the multilayer film structures may be a heat seal layer. Preferably, the heat seal layer comprises at least one ethylene-α-olefin copolymer (EAO) and ethylene vinyl acetate blend (EAO:EVA blend). Suitable α-olefins include C3-C 10Alpha-olefins include, for example, propene, butene-1, pentene-1, hexene-1, methylpentene-1, octene-1, decene-1, and combinations thereof. The heat seal layer is the thickest layer of the multilayer film and can contribute significantly to the puncture resistance of the film. Another desirable property influenced by this layer is the heat seal temperature range. It is preferred that the temperature range for heat sealing the film be as wide as possible. This allows for greater variability in the operation of the heat seal equipment compared to films that have a very narrow range. For example, it is desirable for a suitable film to heat seal over a wide temperature range that provides a heat seal window of 25°C or more.

[0054] Multilayer film structures can also be oxygen permeable by using substantially linear ethylene polymers (SLEPs) alone in the film or in combination with other oxygen permeable film layers such as, for example, ethylene / vinyl acetate (EVA) and / or ethylene / acrylic acid (EAA). These films are preferably prepared with good oxygen permeability, stretchability, elastic recovery and heat seal properties and can be made available to wholesalers and retailers in any conventional form, such as stock rolls, and can be used with conventional packaging equipment.

[0055] The biaxially oriented polymer film of the present disclosure can also include a barrier polymer layer and a tie layer adjacent to the puncture resistant layer, where the puncture resistant layer and the barrier layer and tie layer set of the biaxially oriented polymer film are biaxially stretched at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:1.

[0056] In another embodiment, the multilayer film structure can include an oxygen and / or moisture barrier layer. As used herein, the term "barrier" or "barrier layer" refers to a layer of a multilayer film that functions as a physical barrier against moisture or oxygen molecules. A barrier layer material that is advantageous for packaging oxygen-sensitive materials such as fresh red meat, in combination with other film layers, provides an oxygen gas transmission rate (O2GTR) of less than 70 (preferably 45 or less, more preferably 15 or less) cubic centimeters (cc) per square meter in 24 hours at a temperature of 23°C and 0% relative humidity. When an oxygen barrier layer is required, it is usually provided as a separate layer of the multilayer film, as a core layer sandwiched between the inner heat seal layer and the outer layer, but additional layers can also be included, such as layers to add or modify various properties of the desired film, such as heat sealability, toughness, abrasion resistance, tear resistance, heat shrinkability, peel resistance, stiffness, moisture resistance, optical properties, printability, etc.

[0057] Oxygen barrier materials that may be included in the multilayer thermoplastic film include ethylene vinyl alcohol copolymers (EVOH), metal foils, metallized polyesters, polyacrylonitrile, silica oxide treated polymer films, polyamides, and vinylidene chloride copolymers (PVDC). Preferred oxygen barrier polymers for use with the present disclosure are vinylidene chloride copolymers or vinyl chloride (VC-VDC copolymers) or methyl acrylate (MA-VDC copolymers), as well as vinylidene chloride copolymers with various comonomers such as EVOH.

[0058] The thickness of the monolayer or multilayer film structure can vary, however, for both the monolayer and multilayer film structures described herein, the thickness is typically from about 10 micrometers to about 200 micrometers, preferably from about 20 micrometers to about 150 micrometers), and particularly from about 30 micrometers to about 130 micrometers.

[0059] The multilayer film structure of the present disclosure can also undergo irradiation crosslinking. In the irradiation crosslinking process, the multilayer film structure of the present disclosure can be produced by a blown film process and then exposed to an irradiation source (beta or gamma) at an irradiation dose of up to 50 megarads (Mrad) to crosslink the polymer film. Irradiation crosslinking can be induced before or after final film orientation whenever an oriented film is desired, such as for shrink and skin wrapping, but preferably irradiation crosslinking is induced before final orientation. Irradiation techniques useful for treating the film structures described herein include techniques known to those skilled in the art. Preferably, irradiation is accomplished by using an electron beam (beta) irradiation device at a dose level of about 0.5 Mrad to about 30 Mrad. Shrink film structures produced from the multilayer film structure of the present disclosure are also expected to exhibit improved physical properties due to a lower degree of chain scission resulting from irradiation treatment.

[0060] For the embodiments provided herein, the multilayer thermoplastic film can be prepared using a variety of processes. For example, the multilayer thermoplastic film structure of the present disclosure can be made by using traditional simple bubble or cast extrusion techniques, as well as more sophisticated techniques such as "tenter framing" or "double bubble" or "trapped bubble" processes. "Stretched" and "oriented" are used in the art and are used interchangeably herein, but the orientation is actually the result of the film being stretched, for example, by pressing internal air pressure on a tube or by a tenter frame pulling the edges of the film.

[0061] A simple bubble film process is described, for example, in The Encyclopedia of Chemical Technology, Kirk-Othmer, Third Edition, John Wiley & Sons, New York, 1981, Vol. 16, pp. 416-417 and Vol. 18, pp. 191-192, the disclosures of which are incorporated herein by reference. Processes for producing biaxially oriented films, such as the "double bubble" process described in U.S. Pat. No. 3,456,044 (Pahlke), and other suitable processes for preparing biaxially stretched or oriented films are described in U.S. Pat. Nos. 4,865,902 (Golike et al.), 4,352,849 (Mueller), 4,820,557 (Warren), 4,927,708 (Herran et al.), 4,963,419 (Lustig et al.), and 4,952,451 (Mueller), the disclosures of each of which are incorporated herein by reference.

[0062] As disclosed by Pahlke in U.S. Pat. No. 3,456,044, and compared to the simple bubble process, the "double bubble" or "trapped bubble" film process can significantly increase the orientation of the film in both the machine and transverse directions. The increased orientation results in higher free shrink values ​​when the film is subsequently heated. Also, U.S. Pat. No. 3,456,044 to Pahlke and U.S. Pat. No. 5,059,481 to Lustig et al. (incorporated herein by reference) disclose that low density polyethylene and ultra low density polyethylene materials, respectively, when produced by the simple bubble process, exhibit poor machine and transverse shrink properties, e.g., with a free shrink of about 3% in both directions. However, in contrast to known film materials, particularly those disclosed by Lustig et al. in U.S. Pat. Nos. 5,059,481, 4,976,898, and 4,863,769, and by Smith in U.S. Pat. No. 5,032,463, the disclosure of which is incorporated herein by reference, the unique substantially linear ethylene polymers of the present disclosure exhibit significantly improved simple cell shrink properties in both the machine and cross directions.

[0063] The blow-up ratio used in forming the heat shrinkable biaxially oriented multilayer thermoplastic films of the present disclosure can be from 2: 1 to 10: 1. As will be understood by those skilled in the art, the blow-up ratio is calculated by the formula bubble diameter divided by die diameter.

[0064] Antioxidants (e.g., IRGANOX® 1010 or IRGANOX® 1076 (supplied by BASF), phosphates (e.g., IRGAFOS® 168 (also supplied by BASF)), cling additives (e.g., PIB), SANDOSTAB Additives such as PEPQ™ (supplied by Sandoz), pigments, colorants, fillers, etc. may also be included in the heat shrinkable biaxially oriented multilayer thermoplastic film of the present disclosure. Although not generally required, the multilayer thermoplastic film of the present disclosure may also include additives to enhance antiblocking, release and coefficient of friction properties, including, but not limited to, untreated and treated silicon dioxide, talc, calcium carbonate, and clay, as well as primary, secondary, and substituted fatty acid amides, release agents, silicone coatings, and the like. Still other additives, such as quaternary ammonium compounds alone or in combination with ethylene-acrylic acid (EAA) copolymers or other functional polymers, may also be added to enhance the antistatic properties of the multilayer thermoplastic film of the present disclosure, allowing the shrink film of the present invention to be used, for example, for heavy loads of electronically sensitive goods.

[0065] The multilayer thermoplastic films of the present disclosure may further include recycled and scrap materials and diluent polymers to the extent that the improved shrink film properties discovered by the applicant are not adversely affected. Exemplary diluent materials include, for example, elastomers, rubbers and anhydride modified polyethylenes (e.g., polybutylene and maleic anhydride grafted LLDPE and HDPE), as well as high pressure polyethylenes such as low density polyethylene (LDPE), ethylene / acrylic acid (EAA) interpolymers, ethylene / vinyl acetate (EVA) interpolymers and ethylene / methacrylate (EMA) interpolymers, and combinations thereof.

[0066] The multilayer thermoplastic films of the present disclosure are useful for enhancing their strength, barrier, and / or shrink properties. The multilayer thermoplastic films of the present disclosure may be useful in a variety of packaging and storage applications for non-food and food products, such as primal and subprimal cuts of meat, ham, poultry, bacon, cheese, etc. Preferably, the multilayer thermoplastic films are suitable for use in packaging food items.

[0067] The present disclosure also provides a method for forming a heat shrinkable biaxially oriented multilayer thermoplastic film suitable for use in the manufacture of bags for packaging food articles. The method has a modulus of elasticity of 0.890 g / cm, as determined in accordance with ASTM D-792. 3 ~0.910g / cm 3 and a melt index (MI) of 0.5 g / 10 min to 1.5 g / 10 min as measured by ASTM D-1238, condition 190° C. / 2.16 kg, wherein the polyethylene-based plastomer has a logM 25%The composition has a single SCBD peak at 40-85°C with a comonomer distribution constant value of 60-400 and a mass fraction above 85°C of less than 3%, a ZSVR value of 1.0-5.5, as determined by CEF, and a 100% yield. The method includes: collapsing the first extrusion bubbles to form a first multi-layer structure; passing the first multi-layer structure through a first water bath having a temperature of 5°C-50°C to cool the first multi-layer structure, the first multi-layer structure having a residence time in the water of the first water bath of 0.5-50 seconds; and passing the first multi-layer structure through a second water bath having a temperature of 80°C-100°C to cool the first multi-layer structure. warming the first multi-layer structure coming from the water bath of 100° C., the first multi-layer structure having a residence time in the water of the second water bath of 5 to 50 seconds; heating the first multi-layer structure to a temperature of 60° C. to 120° C.; forming a second extrusion bubble while the first multi-layer structure is heated to a temperature of 60° C. to 120° C., the first multi-layer structure having a blow-up ratio of 2:1 to 10:1 in forming the second extrusion bubble; and collapsing the second extrusion bubble to form a heat shrinkable biaxially oriented multi-layer thermoplastic film.

[0068] definition Density values ​​recited in this disclosure are determined in accordance with ASTM D-792 and are in grams per cubic centimeter (g / cm 3 ) Melt index (MI) values ​​recited in this disclosure are determined according to ASTM D-1238, condition 190°C / 2.16 kg (known as I2). Melt index is inversely proportional to the molecular weight of the polymer. Thus, the higher the molecular weight, the lower the melt index, although the relationship is not linear. Melt index is reported as g / 10 min. Melt index determination is based on the MI value. 10 It can also be carried out at higher weights according to ASTM D-1238, known as 190°C / 10 kg. The term "melt flow ratio" is defined herein in its conventional sense as the ratio of a melt index determination of a higher weight to a melt index determination of a lower weight. 10 If the melt index values ​​of I and I2 are measured, the melt flow ratio is I 10 Conveniently designated / I2.

[0069] The term "composition", as used, is inclusive of a mixture of materials which comprise the composition, as well as reaction products and decomposition products formed from the materials of the composition.

[0070] The term "blend" or "polymer blend" as used means an intimate physical mixture (i.e., without reaction) of two or more polymers. A blend may or may not be miscible (not phase separated at the molecular level). A blend may or may not be phase separated. A blend may or may not contain one or more domain configurations as determined from transmission electron spectroscopy, light scattering, x-ray scattering, and other methods known in the art. A blend may be affected by physically mixing two or more polymers on a macro level (e.g., melt blending resins or compounds) or micro level (e.g., co-forming in the same reactor).

[0071] The term "linear" refers to a polymer in which the polymer backbone of the polymer lacks measurable or demonstrable long chain branching, e.g., the polymer may be substituted with less than 0.01 long chain branches per 1000 carbons.

[0072] The term "polymer" refers to a polymeric compound prepared by polymerizing monomers, whether the monomers are the same or different. Thus, the generic term polymer encompasses the term "homopolymer", which is usually used to refer to a polymer prepared from only one type of monomer, and the term "interpolymer", which is defined. The term "ethylene / α-olefin polymer" refers to an interpolymer as described.

[0073] The term "interpolymer" refers to polymers prepared by the polymerization of at least two different types of monomers. The generic term interpolymer includes copolymers, which are typically used to refer to polymers prepared from two different types of monomers, and polymers prepared from three or more different types of monomers.

[0074] The term "ethylene-based polymer" refers to a polymer that contains greater than 50 mole percent polymerized ethylene monomer (based on the total amount of polymerizable monomers) and, optionally, may contain at least one comonomer.

[0075] The term "ethylene / α-olefin interpolymer" refers to an interpolymer that contains greater than 50 mole percent polymerized ethylene monomer (based on the total amount of polymerizable monomers) and at least one α-olefin.

[0076] Although "stretched" and "oriented" are used in the art and are used interchangeably herein, the orientation is actually the result of the film being stretched, for example, by imposing internal air pressure on a tube or by a tenter frame pulling on the edges of the film.

[0077] Shrink temperatures within the range of about 40 to about 140° C., particularly about 50 to about 125° C., and more specifically about 60 to about 110° C., are suitable in the present disclosure.

[0078] The term "residual crystallinity" is used herein to refer to the crystallinity of a polymer film at a particular stretching temperature. Residual crystallinity is determined using a Perkin-Elmer DSC 7 set for a first heat at 10°C / min of a water-quenched compression molded film sample of the polymer. The residual crystallinity of an interpolymer at a particular temperature is determined by measuring the heat of fusion between that temperature and the full melting temperature using a partial area technique and dividing the heat of fusion by 292 Joules / gram. The heat of fusion is determined by computer integration of the partial area using Perkin-Elmer PC Series Software Version 3.1.

[0079] As used herein, the term "shrink control layer" refers to a film layer that provides or controls the shrink response. Such a layer is inherent in all heat shrink films. In a monolayer heat shrink film, the shrink control layer is the film itself. In a multilayer heat shrink film, the shrink control layer is typically the core or inner film layer, and is typically the thickest film layer. See, for example, WO95 / 08441.

[0080] The term "substantially unoriented form" is used herein in reference to the fact that a certain amount of orientation is typically imparted to the film during normal manufacturing. It therefore means that the manufacturing step itself is not used to impart the degree of orientation required for the desired or required shrink response. The present disclosure is considered generally applicable to operations in which the manufacturing and orientation steps are separable and occur simultaneously. However, the present disclosure is preferably directed to an additional, separate orientation step, whether such softening, melting, or irradiating, before substantial orientation is imparted, which is required beyond the creation of tubes, socks, webs, or flat sheets.

[0081] The following examples are provided for illustrative purposes and are not intended to suggest any particular limitations of the present disclosure. EXAMPLES

[0082] The following "Original Structures" and "Inventive Structures" are prepared using the double bubble or trapped bubble process according to the detailed description above, generally utilizing the apparatus shown in FIG. 1. In FIG. 1, the element numbers represent the following elements of the apparatus: 100 - extruder, 102 - tape, 104 - water bath (90°C), 106 - heater, 108 - drawing process. In the following examples, all layers were extruded (in the multilayer examples, coextruded) as a primary tube that was cooled upon exiting the die, for example, using a cold water fountain (10-20°C). This primary tube was then reheated in a hot water bath (90°C) and then reheated to the extraction temperature by radiant heaters (60-120°C) for biaxial orientation achieved by an air cushion, itself heated by a transverse flow through a heated porous tube arranged concentrically around the moving primary tube. Cooling was achieved by a concentric air ring. Draw point temperatures, bubble heating and cooling rates and orientation ratios were typically adjusted to maximize bubble stability and throughput for the desired amount of stretching or orientation. All percentages are weight percent unless otherwise noted.

[0083] The "Original Structure" was made with the following "A / B / C" multi-layer structure, with the weight percentage of each layer being 40% / 30% / 30%, respectively: Layer A (inner layer) is formed from a 70% / 30% blend of Affinity™ PL 1880G (The Dow Chemical Company) and Attané™ 4203G (The Dow Chemical Company), respectively; Layer B is formed from Elvax® 470 (Dupont); Layer C is formed from Affinity™ PL 1880G (The Dow Chemical Company) and serves as the puncture resistant layer.

[0084] The "Inventive Structure" was made having the following "A / B / C" multi-layer structure, with the weight percentages of each layer being 40% / 30% / 30%, respectively. Layer A (inner layer) is formed from a 70% / 30% blend of Affinity™ PL 1880G (The Dow Chemical Company) and Attané™ 4203G (The Dow Chemical Company), respectively. Layer B is formed from Elvax® 470 (Dupont). Layer C is formed from Affinity™ PL1860G (The Dow Chemical Company) and serves as an example of a puncture resistant layer of the present disclosure.

[0085] The physical properties of the materials listed above can be found in Table 1. [Table 2]

[0086] Traditional Gel Permeation Chromatography (GPC) The chromatography system consisted of a PolymerChar GPC-IR (Valencia, Spain) high temperature GPC chromatograph equipped with an internal IR5 infrared detector (IR5) coupled to a Precision Detectors (Now Agilent Technologies) two-angle laser light scattering (LS) detector model 2040. For all light scattering measurements, a 15 degree angle was used for measurement purposes. The autosampler oven compartment was set at 160 degrees Celsius and the column compartment was set at 150 degrees Celsius. The columns used were three Agilent "Mixed B" 30 cm 20 micron linear mixed bed columns. The chromatography solvent used was 1,2,4-trichlorobenzene with 200 ppm butylated hydroxytoluene (BHT). The solvent source was nitrogen injected. The injection volume used was 200 microliters and the flow rate was 1.0 milliliters / min.

[0087] Standards were purchased from Agilent Technologies. Polystyrene standards were prepared at 0.025 grams in 50 milliliters of solvent for molecular weights equal to or greater than 1,000,000, and 0.05 grams in 50 milliliters of solvent for molecular weights less than 1,000,000. The polystyrene standards were dissolved at 80 degrees Celsius for 30 minutes with gentle agitation. The peak molecular weight of the polystyrene standards was determined (as described in Williams and Ward, J. Polym. Sci., Polym. Let., 6, 621 (1968)):

number

[0088] A polynomial between the third and fifth order was used to fit each polyethylene equivalent calibration point. A small adjustment (approximately 0.415 to 0.44) was made to A to correct for column resolution and band broadening effects, such that the NIST standard NBS 1475 is obtained at 52,000 MW.

[0089] A total plate count of the GPC column set was performed with Eicosane (prepared at 0.04 g in 50 milliliters of TCB and dissolved for 20 minutes with gentle agitation).

number

number

[0090] Samples were prepared semi-automatically using the PolymerChar "Instrument Control" software, with a target sample weight of 2mg / ml, by adding solvent (containing 200ppm BHT) via the PolymerChar high temperature autosampler to a septa-capped vial that had been pre-sparged with nitrogen. Samples were dissolved at 160 degrees Celsius with "slow" shaking for 2 hours.

[0091] Mn (GPC) , Mw (GPC) , and Mz (GPC) The calculations were based on GPC results using PolymerChar GPCOne™ software, the internal IR5 detector (measurement channel) of the PolymerChar GPC-IR chromatograph according to Equations 4-6 using baseline-subtracted IR chromatograms at each equally spaced data collection point (i), and the polyethylene equivalent molecular weights obtained from a narrow standard calibration curve at point (i) from Equation 1.

number

number

number

[0092] To monitor deviations over time, a flow marker (decane) was introduced into each sample via a micropump controlled by the PolymerChar GPC-IR system. This flow marker (FM) was used to linearly calibrate the pump flow rate (Flow (apparent)) of each sample by aligning the respective decane peak in the sample (RV (FM sample)) with the decane peak in the narrow standard calibration (RV (FM calibrated)). Any change in time of the decane marker peak is thus assumed to be related to a linear shift in flow rate (Flow (effective)). To facilitate the highest accuracy of the RV measurement of the flow marker peak, a least squares fitting routine is used to fit the peaks of the flow marker concentration chromatogram to a quadratic equation. The first derivative of the quadratic equation is then used to determine the true peak position. After calibrating the system based on the flow marker peaks, the effective flow rate (relative to the narrow standard calibration) is calculated as in Equation 7. Processing of the flow marker peaks was performed by PolymerChar GPCOne™ software. An acceptable flow correction is that the effective flow rate should be within + / - 2% of the apparent flow rate.

[0093] Flow (effective) = Flow (apparent) * (RV(FM calibrated) / RV(FM sample)) (Equation 7)

[0094] Calculation of quadrants from MWD by GPC The chromatographic system, analytical conditions, column set, column calibration and calculation and distribution of conventional molecular weight moments were performed according to the methods described in Gel Permeation Chromatography (GPC).

[0095] The plotted molecular weight distribution from GPC (dWf / dLogM vs. LogM) has, by definition, an area equal to 1. The plot was divided into four equivalent area intercepts (weight fraction = 0.25) integrated from high molecular weight to low molecular weight. For each quadrant (25%, 50%, 75%, 100%), the average logM was determined as per Equations 8A-8D below.

number

number

number

number

[0096] Here, the MWD region is integrated from the highest detectable logMw to the lowest detectable logMw at each dWf / dLogM, and each slice (i) represents 0.01 LogMw in width. The average GPC molecular weight for each quadrant is calculated as follows: 10^LogM 象限 This value differs from the mathematical mean obtained by taking the average of 10^LogMi at each slice (i) in the quadrant. The following GPC graph (Figure 2) shows the intermediate molecular weight distribution of Affinity™ PL 1880G, Affinity™ PL 1860G and Attané™ 4203G. Looking at the average molecular weight numbers of the grades, it can be noticed that when comparing Affinity™ PL 1880G and Affinity™ PL 1860G, the main difference is found in Mz, influenced by the high molecular weight fraction present in the final resin. [Table 3] [Table 4]

[0097] One extruder was used for each layer. Each extruder was connected to an annular coextrusion die from which the thermoplastic resins were coextruded to form the primary tube. The resin mixture for each layer was fed from a hopper to an attached single screw extruder, where the mixture was thermoplasticized and extruded through a three-layer coextrusion die into the primary tube. The extruder barrel temperature for layer B was about 120-150°C, for layer A and for layer C was about 140-165°C. The coextrusion die temperature profile was set at about 160-180°C. The processing conditions were obtained using 100 kg / hr, initial thickness of 500 microns, final thickness of 70 microns, and the material temperature before the second bubble stretch is 116°C.

[0098] To evaluate the benefits of using a puncture resistant layer of the present disclosure, in this case Affinity™ PL 1860G, the following puncture tests were performed: ASTM F1306.90 - Sharp edge puncture and round puncture test using the Dow method. [Table 5]

[0099] The inventive structure was found to have improved puncture force and puncture energy compared to the original structure. The present application also relates to the following aspects: (1) A heat shrinkable biaxially oriented multilayer thermoplastic film, the multilayer thermoplastic film having a compressibility of 0.890 g / cm 3 ~0.910g / cm 3 and a melt index (MI) measured at 190° C. / 2.16 kg of 0.20 g / 10 min to 1.5 g / 10 min, The logM in the upper 25% of the GPC quadrants with values ​​between 5.1 and 5.7 25% and, A medium molecular weight distribution (Mw / Mn) of 2.5 to 3 and a Mz / Mw value of 2 to 2.5; a single SCBD peak between 40 and 85°C with a comonomer distribution constant value between 60 and 400 and a mass fraction above 85°C of less than 3% as determined by CEF; A ZSVR value of 1.0 to 5.5; The multilayer thermoplastic film is a heat shrinkable biaxially oriented multilayer thermoplastic film that is biaxially oriented at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:1. (2) The multilayer thermoplastic film according to (1) above, wherein the polyethylene-based plastomer has a melt index (MI) measured by ASTM D-1238, condition 190°C / 2.16 kg, of 0.75 g / 10 min to 1 g / 10 min. (3) The polyethylene plastomer has a viscosity of 0.900 g / cm, as determined in accordance with ASTM D-792. 3 ~0.910g / cm 3 The multilayer thermoplastic film according to (1) or (2) above, having a density of (4) The multilayer thermoplastic film according to any one of (1) to (3) above, wherein the puncture resistant layer further comprises 5 weight percent to 50 weight percent of an ethylene / vinyl acetate copolymer, based on the weight of the blend. (5) The multilayer thermoplastic film according to any one of (1) to (3) above, wherein the polyethylene-based plastomer of the puncture-resistant layer is blended with 5 weight percent to 50 weight percent of a heterogeneously branched ultra-low density polyethylene or a heterogeneously branched very-low density polyethylene, based on the weight of the blend. (6) The multilayer thermoplastic film according to any one of (1) to (3) above, wherein the polyethylene-based plastomer of the puncture-resistant layer is an ethylene interpolymer having at least one α-olefin having 3 to 20 carbon atoms. (7) The multilayer thermoplastic film according to any one of the above (1) to (3), wherein the polyethylene-based plastomer of the puncture-resistant layer is an ethylene / α-olefin copolymer. (8) The multilayer thermoplastic film according to (7) above, wherein the ethylene / α-olefin copolymer is an ethylene / 1-octene copolymer. (9) The multilayer thermoplastic film according to any one of (1) to (8) above, further comprising a second polymer layer adjacent to the puncture-resistant layer, and the puncture-resistant layer and the second polymer layer of the multilayer thermoplastic film are biaxially stretched at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:1. (10) The multilayer thermoplastic film according to (9), wherein the second polymer layer is formed from a polymer selected from the group consisting of ultra-low density polyethylene, very-low density polyethylene, ethylene / α-olefin interpolymer, ethylene-vinyl acetate copolymer, polyamide, copolymer of polyvinylidene chloride, ethylene vinyl alcohol or linear low density polyethylene grafted maleic anhydride. (11) The multilayer thermoplastic film according to (9) above, further comprising a third polymer layer disposed between the puncture-resistant layer and the second polymer layer, and the puncture-resistant layer, the second polymer layer and the third polymer layer of the multilayer thermoplastic film are biaxially stretched at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:1. (12) The multilayer thermoplastic film according to (9), wherein the second polymer layer and the third polymer layer are independently formed from a polymer selected from the group consisting of ultra-low density polyethylene, very-low density polyethylene, ethylene / α-olefin interpolymer, ethylene-vinyl acetate copolymer, polyamide, copolymer of polyvinylidene chloride, ethylene vinyl alcohol or linear low density polyethylene grafted maleic anhydride. (13) The multilayer thermoplastic film according to (12) above, wherein the polymer of the second polymer layer is structurally different from the polymer of the third polymer layer. (14) The multilayer thermoplastic film according to (12) above, wherein the third polymer layer is an ethylene-vinyl acetate copolymer and the second polymer layer comprises an ethylene / α-olefin interpolymer and an ultra-low density polyethylene. (15) The multilayer thermoplastic film according to any one of (1) to (14) above, wherein the biaxially oriented polymer film further comprises a barrier polymer layer and a tie layer adjacent to the puncture resistant layer, and the set of the puncture resistant layer and the barrier and tie layer of the biaxially oriented polymer film is biaxially stretched at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:1. (16) The multilayer thermoplastic film according to any one of (1) to (15) above, which is prepared by a double bubble process. (17) The multilayer thermoplastic film according to any one of (1) to (16) above, which is suitable for use in packaging food products. (18) The polyethylene plastomer has a logM 25% The multilayer thermoplastic film according to any one of the above (1) to (17), (19) A process for forming a heat shrinkable biaxially oriented multilayer thermoplastic film suitable for use in the manufacture of bags for packaging food items, said process comprising: 0.890 g / cm3 determined in accordance with ASTM D-792 3 ~0.910g / cm 3 and a melt index (MI) of 0.20 g / 10 min to 1.5 g / 10 min as measured by ASTM D-1238, Condition 190° C. / 2.16 kg, wherein the polyethylene-based plastomer comprises: The logM in the upper 25% of the GPC quadrants with values ​​between 5.1 and 5.7 25% and, A medium molecular weight distribution (Mw / Mn) of 2.5 to 3 and a Mz / Mw value of 2 to 2.5; a single SCBD peak between 40 and 85°C with a comonomer distribution constant value between 60 and 400 and a mass fraction above 85°C of less than 3% as determined by CEF; and forming a porcelain sintered body having a ZSVR value of 1.0 to 5.5. collapsing the first extrusion bubbles to form a first multi-layer structure; cooling the first multi-layer structure by passing the first multi-layer structure through a first water bath having a temperature between 5° C. and 50° C., wherein the first multi-layer structure has a residence time in the water of the first water bath between 0.5 and 50 seconds; warming the first multi-layer structure coming from the first water bath by passing the first multi-layer structure through a second water bath having a temperature of 80° C. to 100° C., the first multi-layer structure having a residence time in the water of the second water bath of 5 to 50 seconds; Heating the first multilayer structure to a temperature between 60°C and 120°C; forming a second extrusion bubble while the first multi-layer structure is heated to a temperature of 60°C to 120°C, the first multi-layer structure having a blow-up ratio of 2:1 to 10:1 when forming the second extrusion bubble; collapsing said second extruded bubbles to form said heat shrinkable biaxially oriented multilayer thermoplastic film.

Claims

1. 1. A heat shrinkable biaxially oriented multilayer thermoplastic film, said multilayer thermoplastic film having a compressibility of 0.890 g / cm, as determined in accordance with ASTM D-792. ３ ~0.910g / cm ３ and a melt index (MI) measured at 190° C. / 2.16 kg of 0.20 g / 10 min to 1.5 g / 10 min, as measured by ASTM D-1238, wherein the polyethylene plastomer is The upper 25% of the GPC quadrant with values ​​between 5.1 and 5.7 ２５％ and, an intermediate molecular weight distribution (Mw / Mn) of 2.5 to 3 and an Mz / Mw value of 2 to 2.5; having a single SCBD peak between 40 and 85° C. with a comonomer distribution constant value between 60 and 400 and a mass fraction above 85° C. of less than 3%, as determined by CEF; and a ZSVR value of 1.0 to 5.5; The multi-layer thermoplastic film is a heat shrinkable biaxially oriented multi-layer thermoplastic film that is biaxially oriented at a temperature of 60° C. to 120° C. with a blow-up ratio of 2:1 to 10:

1.

2. 10. The multilayer thermoplastic film of claim 1, wherein the polyethylene-based plastomer has a melt index (MI) of 0.75 g / 10 min to 1 g / 10 min as measured by ASTM D-1238, condition 190° C. / 2.16 kg.

3. The polyethylene plastomer has a modulus of 0.900 g / cm3, as determined in accordance with ASTM D-792. ３ ~0.910g / cm ３ 3. The multilayer thermoplastic film of claim 1, having a density of

4. the puncture resistant layer further comprises 5 weight percent to 50 weight percent of an ethylene / vinyl acetate copolymer, based on the weight of the blend; or the polyethylene-based plastomer of the puncture resistant layer is blended with 5 weight percent to 50 weight percent of a heterogeneously branched ultra-low density polyethylene or a heterogeneously branched very-low density polyethylene, based on the weight of the blend; or 4. The multilayer thermoplastic film of claim 1, wherein the polyethylene-based plastomer of the puncture resistant layer is an ethylene interpolymer having at least one α-olefin of 3 to 20 carbon atoms, or the polyethylene-based plastomer of the puncture resistant layer is an ethylene / α-olefin copolymer.

5. The multilayer thermoplastic film of claim 4, wherein the ethylene / α-olefin copolymer is an ethylene / 1-octene copolymer.

6. 6. The multilayer thermoplastic film of claim 1, further comprising a second polymer layer adjacent to the puncture resistant layer, and wherein the puncture resistant layer and the second polymer layer of the multilayer thermoplastic film are biaxially stretched at a temperature of 60°C to 120°C with a blow-up ratio of 2:1 to 10:

1.

7. (i) the second polymer layer is formed from a polymer selected from the group consisting of ultra-low density polyethylene, very-low density polyethylene, ethylene / α-olefin interpolymer, ethylene-vinyl acetate copolymer, polyamide, copolymer of polyvinylidene chloride, ethylene vinyl alcohol or linear low density polyethylene grafted maleic anhydride; or (ii) the multilayer thermoplastic film further comprises a third polymer layer disposed between the puncture resistant layer and the second polymer layer, and the puncture resistant layer, the second polymer layer and the third polymer layer of the multilayer thermoplastic film are biaxially stretched at a temperature of 60° C. to 120° C. with a blow-up ratio of 2:1 to 10:1; or (iii) the multilayer thermoplastic film further comprises a third polymer layer disposed between the puncture resistant layer and the second polymer layer, the second polymer layer and the third polymer layer being independently formed from a polymer selected from the group consisting of ultra-low density polyethylene, very-low density polyethylene, ethylene / α-olefin interpolymer, ethylene-vinyl acetate copolymer, polyamide, copolymer of polyvinylidene chloride, ethylene vinyl alcohol, or linear low density polyethylene grafted maleic anhydride; The multilayer thermoplastic film of claim 6.

8. the multilayer thermoplastic film further comprises a third polymer layer disposed between the puncture resistant layer and the second polymer layer; (i) the polymer of the second polymer layer is a structurally distinct polymer from the polymer of the third polymer layer; or 8. The multilayer thermoplastic film of claim 7, wherein (ii) the third polymer layer is an ethylene-vinyl acetate copolymer and the second polymer layer comprises an ethylene / α-olefin interpolymer and an ultra-low density polyethylene.

9. the biaxially oriented multilayer thermoplastic film further comprises a barrier polymer layer and an adhesion promoting tie layer adjacent to the puncture resistant layer, and the puncture resistant layer and the set of barrier and tie layers of the biaxially oriented multilayer thermoplastic film are biaxially oriented at a temperature of 60° C. to 120° C. with a blow-up ratio of 2:1 to 10:1; or The multilayer thermoplastic film is prepared by a double bubble process; or the multilayer thermoplastic film is for packaging food items; or The polyethylene-based plastomer has a log M ２５％ The multilayer thermoplastic film of any one of claims 1 to 8, having

10. 1. A method for forming a heat shrinkable biaxially oriented multilayer thermoplastic film suitable for use in the manufacture of bags for packaging food products, the method comprising: 0.890 g / cm3 as determined in accordance with ASTM D-792 ３ ~0.910g / cm ３ and a melt index (MI) of 0.20 g / 10 min to 1.5 g / 10 min as measured by ASTM D-1238, Condition 190° C. / 2.16 kg, wherein the polyethylene-based plastomer is The upper 25% of the GPC quadrant with values ​​between 5.1 and 5.7 ２５％ and, an intermediate molecular weight distribution (Mw / Mn) of 2.5 to 3 and an Mz / Mw value of 2 to 2.5; a single SCBD peak between 40 and 85° C. with a comonomer distribution constant value between 60 and 400 and a mass fraction above 85° C. of less than 3% as determined by CEF; a ZSVR value of 1.0 to 5.5; collapsing the first extrusion bubbles to form a first multi-layer structure; cooling the first multi-layer structure by passing the first multi-layer structure through a first water bath having a temperature of 5° C. to 50° C., wherein the first multi-layer structure has a residence time in the water of the first water bath of 0.5 to 50 seconds; Passing the first multi-layer structure through a second water bath having a temperature of 80° C. to 100° C. to warm the first multi-layer structure coming from the first water bath, wherein the first multi-layer structure is warming, having a residence time of 5 to 50 seconds in the water of the second water bath; heating the first multi-layer structure to a temperature between 60° C. and 120° C.; forming a second extruded bubble with the first multi-layer structure heated to the temperature of 60°C to 120°C, the first multi-layer structure having a blow-up ratio of 2:1 to 10:1 when forming the second extruded bubble; collapsing said second extruded bubbles to form said heat shrinkable biaxially oriented multilayer thermoplastic film.

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