CA1303790C

CA1303790C - Skin packaging film

Info

Publication number: CA1303790C
Application number: CA000562674A
Authority: CA
Inventors: Alfred P. Engelmann; George Jack Mccrary, Jr.; Stephen Leroy Fowler; Marvin Russell Havens
Original assignee: WR Grace and Co Conn
Current assignee: WR Grace and Co Conn
Priority date: 1987-07-02
Filing date: 1988-03-28
Publication date: 1992-06-16
Anticipated expiration: 2009-06-16
Also published as: GB8815708D0; GB2206890B; JPH01105739A; NZ225191A; ZA884624B; BR8803295A; GB2206890A; KR890002290A; AU1850988A

Abstract

ABSTRACT

Disclosed is a skin packaging film for skin packaging high profile and/or heavy articles. The film comprises linear ethylene/alpha-olefin co-polymer. In one embodiment, the film is antistatic and may be employed for skin packaging of electro-static sensitive items such as circuit boards.

Description

i303790 SKIN PACKAOE FILM

The present invention relates to a specific filn as a skin package film for high-profile and/or heav,v articles, both food and non-food items.
More particularly the film cc~,prises linear ethylene/alpha-olefin copolymer.
In a preferred embodiment, the film is antistatic or static dissipative, and may be e~,ployed for skin packaging electrostatic sensitive devices, such as circuit boards.

BACKGROUND OF THE INVENTION

Skin packaging is essentially a vacuum forming process. In a typical process, a sheet of thermoplastic film ls placed in a frame, and below the frame is a vacuum plate upon which a piece of support pervious to gases such as a backing board is placed. The product to be skin packaged is positioned on top of the backing board and heat is applied to the thermo-plastic film in the frame. When the film has been heated to become sufficiently soft, the frame is lowered and the plastic sheet drapes itself over the product. As this happens, a partial vacuum is created through the vacuum plate and the air underneath the plastic film is withdra~n through the backing board. The air pressure differential between the top and the bottom of the plastic sheet causes the sheet to be tightly pressed around the product. The support is adapted to bond to the plastic sheet.
Typically, the film may be thermally bonded to the support, or the film may be coated with a glue or the backing board may be so coated. Where the two contact each other, a strong bond is formed resulting in a package in which the product is tightly held to the support for safe shipping and for sub-sequent rack display in retail stores.404/870608/4/1 Vacuum skin packaging differs from the above described skin packaging process in that both the thermoplastic film and the support are impervious to gases and the resulting package can be evacuated and hermeti-cally sealed, if desired. The same end result is sought, i.e. the product is to be tightly held by the film to the backing board. The vacuum skin packaging process generally employes a vacuum chamber with an open top. The product on an impervious backing board is placed on a platform within the vacuum chamber. The top of the chamber is then covered by a sheet of film which is clamped tightly against the chamber to form a vacuum type closure.
The chamber is evacuated while the film is heated to forming and softening temperatures. The platform can then be raised to drive the product into the softened film and air pressure can be used above the film to force it tightly around the product.

The conventional method employes a backing board which is porous or which is perforated to make it pervious to gases so that the vacuum may be drawn directly through the backing board.

The term "vacuum" as used herein means a differential fluid pressure where the fluid can be either a gas or a liquid. The term "skin packaging" as used herein is intended to refer to vacuum packaging pro-cesses as described above, regardless of whether the support is pervious orimpervious. Typically the support is made of a cardboard coated with adhesive polymer so that the film sheet will adhere as the sheet is heated and draped over the article being skin packaged and a differential pressure is applied.

Various patents describe skin packaging machinery and methods.
Representative patents are French Pat. No. 1,258,357 (Bresson) (March 6, 1961), French Pat. No. 1,286,018 (Laroch Freres, Ltd.) (January 22, 1962), Australian Pat. No. 245,774 (Colbro Proprietary Ltd., and Cole and Son Proprietary Ltd.) (July 16, 1963), U.S. Pat. No. 3,491,504 (Young et al) (January 27, 1970), U.S. Pat. 3,545,163 (M~haffy et al) (December 8, 1970), U.S. Pat. No. 3,694,991 (Perdue et al) (October 3, 1972), and U.S. Pat. No.
4,537,011 (Bortolani et al) (August 27, 1985).
H~wever, it is noted that the film of the invention may be employed with various other types of skin i303790 packaging machinery, such as the VS~44 marketed by the Cryovac Division of W. R. Grace or the PORT-A-VAC marketed by AmPak. The film of the invention is not intended to be limited to skin packaging employing only the machinery mentioned herein.

Skin packaging techniques are often disadvantageous in that an excess portion of film is undesirably wrinkled on evacuation and the packaged material or article becomes irregular in shape, thus producing a poor external appear~nce. In addition, the wrapping film is apt to be broken in the portions folded and wrinkled. It has been ascertained in actual practice that as the film thins in the course of the vacuum skin packaging process, conventional films, due to poor tensile strength and poor elongation, tend to be broken when subjected to high stretch or draw ratios at particular projections or recesses randomly arranged on the material being packaged. The breaking can occur during the packaging or afterwards during handling of the packaged product. Methods and films are thus unfavorable fron a practical point of view. There is accordingly a strong demand for improvement in the packaging films and ~ethods.

Conventional l~w density polyethylene (LDPE) is typically used for skin packaging, and attempts to provide specific improved skin packaging films have been made in the past. For instance, disclosed in U.S. Pat. No.
4,275,544 (Hisazumi et al assignors to Kureha) (June 30, 1981) is an im-proved method of vacuum packaging by using a specific laminated filn as a package fi~m, the laminated film being conposed of a plastically deformable layer of a synthetic resin having a yield stress more than 50 kg/cm2 at a temperature of 23C. and an elongation of less than 30% at elastic limit at a shaping temperature of 50 to 180C. and an elastic layer of a synthetic resin having an elongation of more than 40~ at elastic limit at the shaping temperature. Also, disclosed in U.S. Pat. 4,375,851 (Paulos assignor to Bemis) (March 8, 1983) is a skin packaging material composed of a film of thermoplastic material having a reinforcement consisting of strands (in the form of netting, or all extending in one direction parallel to one another) adapted on exposure for an appropriate time interval to a source of heat to have both the film and strands heat up to a forming temperature for being ; 404/870608/4/3 1303~90 skin packaged around an article on a substrate, with the strands less ex-stensible than the film on equal heating of the film and strands, and the skin packaging of articles utilizing said material in such nanner that the strands flare out fr~m the article at the base of the article to provide a broader base of support for the article and to prevent undue thinning of the fi~m. Also? it is kncwn fron U.S. Pat. 4,590,741 (Long et al assignors to General Dynamics) (May 27, 1986) to skin package electrostatically sensitive items with a 3-layer fi~m including first and second outer layers of heat-sealable, electrically semi-conductive polyethylene each having a surface resisivity exceeding lX1016 ohms per square, and a middle layer of heat-sealable polyethylene sandwiched between and bonded to said first and second outer layers and impregnated with a sloughable, electrically-conductive material providing said middle layer with a volume resisivity no re than lX103 ohms per centimeter, wherein said electrically-conductive material is prevented from sloughing to contaminate said item by said first or said second semiconductive polyethylene layer.

Accordingly, an object of this invention is to provide a suitable film for skin packaging of products, which film exhibits high tensile strength and elongation properties even at high stretch or draw ratios, whereby it is sufficiently deformable so that it can conform to the shape of the high-profile and/or heavy product being packaged by deformation without breaking. In other words, the fi~m possesses an excellent deep draw feature affording a high draw ratio. It is another object of this invention to provide a skin packaging film for packing high profile and/or heavy products which film has antistatic characteristics. Thus, it is an aspect of the film that the film serves well as a material for packaging articles which typically have sharp projections such as bone-in meat, electronic components, and the like. The Eilms in accordance with the present in-vention also typically have excellent see-through properties which is ad-vantageous for reading code numbers preprinted on a product wrapped with the fi~m. The films often exhibit very good adhesion to the support, particularly thermal bonding when the support is surlyn-coated cardboard.

SUMMARY OF T~E INVENTION
Therefore, the present invention provides a skin packaging process for packaging an electrostatically sensitive item comprising: (a) placing the item to ~e packaged on a support; (b) positioning a film above said item; (c) heating the film; (d) drawing a vacuum between said film and said support;
and (e) drawing the film over and around the item forminq a heat seal with the support; (f) wherein said film comprises an antistatic linear ethylene~alpha-olefin copolymer film and wherein said linear ethylene~alpha-olefin copolymer is a blend with one or more antistatic agents chosen from (a) one or more fatty acid esters of polyhydroxy alcohols, (b) one or more polyalkoxylated compounds, or a mixture of (a) and (b).
The present invention also provides a skin packaging process for packaging an electrostatlcally sensitive item comprising: (a) placing the item to be packaged on a support;
(b) positioning a film above said i~em; (c) heating the film;
(d) drawing a vacuum between said film and said support; and (e) drawing the film over and around the item forming a heat seal with the support; (f) wherein said film comprises an antistatic linear ethylene/alpha-olefin copolymer film and wherein said linear ethylene/alpha-olefin copolymer is in blend with glycerol monostearate, polyethoxylated cetyl alcohol, and polyethylene oxide.

It is a feature of the film of the invention that it has a high draw ratio of about 20:1 or higher and thus can be employed to skin package high profile objects.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic representation of a skin packaged, high profile object of rectangular cross-section in the direction horizontal to the support.

FIG. 2 is a schematic representation of a skin packaged, high profile sharpened pencil.

DETAILED DESCRIPTION OF THE INVENTION

The film of the present invention exhibits excellent draw ratios and stretch whereby it is sufficiently deformable so that it can be employ-ed to skin package high profile and/or heavy objects. By "heavy", it is intended to mean objects having a weight of about 10 pounds (about 22 kg) or more, more preferably about 15 pounds (about 33 kg) or more, more preferably about 20 pounds (44 kg) or more. By "high profile", it is intended to mean objects having a vertical dimension:minimum horizontal dimension ratio of about 20:1 or more, for instance, an essentially cylindrical object having a height of about 20 inches (50.8 cm) in the direction substantially vertical (i.e. substantially perpendicular) to the support and a base diameter of about 1 inch (2.5 cm) in the direction substantially horizontal to the support. The film exhibits an excellent deepdraw, and will skin package objects with a draw ratio of the vertical dimension:minimum horizontal dimension of the object of about 20:1 or higher, more preferably above about 25:1, most preferably above about 30:1. In a preferred embodiment as ~"
. ;'r ~

13(~3'790 illustrated in Example I f) below, the deep draw ratio is about 64:1. Con-ventional LDPE works at 16:1 as can be seen in Table IIIB below, but splits at 26:1, as can be seen in Table IIIC below. Of course, the film of the invention can be en~ployed, if desired, to skin package objects of lesser weight or shallow profile objects.

The fi~n of the present invention comprises the polyethylene, linear ethylene/alpha-olefin copolymer. The linear ethylene/alpha-olefin copolymer may be blended with one or more suitable other polymers. Suitable other polymers are further described below. The term "linear low density polyethylene" (LLDPE) as used herein, for the linear ethylene/alpha-olefin employed in the present invention, refers to the newer copolymers of ethylene with one or more comonomers selected from C4 to C10 alpha olefins such as butene-l, pentene-l, 4-methyl-pentene-1, hexene-l, octene-l, etc. in which the lecules thereof comprise long chains with few side chains branches or cross-linked structures achieved by low pressure polymerization.
The side branching which is present will be short as compared to non-linear polyethylenes. The molecular chains of a linear polymer may be intertwined, but the forces tending to hold the molecules together are physical rather than chemical and thus may be weakened by energy applied in the form of heat. Linear low density polyethylene has a density preferably in the range of from about 0.911 g/cc to about 0.928 g/cc for film making purposes. The melt flow index of linear low density polyethylene generally ranges form ; between about 0.1 to about 10 grams per ten minutes and preferably between from about 0.5 to about 3.0 grams per ten minutes. Linear low density polyethylene resins of this type are commercially available and are manufactured in low pressure vapor phase and liquid phase processes using transition metal catalysts. Also, very low density linear low density polyethylenes (VLDPE) may be employed, and such typically have a density fr~n about 0.910 g/cc to about 0.860 g/cc, or even lower.

30Suitable other polymers which may be blended with the linear ethylene/alpha-olefin include, but are not limited to, polyethylenes other than linear ethylene/alpha olefins, ethylene vinyl acetates, and ethylene alkyl acrylates. Polyethylenes having densities ranging from about 0.900 g/cc to about 0.928 g/cc are called low density polyethylenes (LDPE) while 35those having densities from about 0.929 g/cc to about 0.940 g/cc are called i30~

medi~m density polyethylenes (MDPE), and those having densities from about 0.941 g/cc to about 0.965 glcc and over are called high density poly-ethylenes (HDPE). The older, classic low density types of polyethylenes are usually polymerized at high pressures and temperatures whereas the older, classic high density types are usually polymerized at relatively low temperatures and pressures. Ethylene vinyl acetate copolymers (EVA) are formed from ethylene and vinyl acetate monomers wherein the ethylene derived units in the copolymer are present in major a~.ounts and the vinyl acetate derived units in the copolymer are present in minor amounts. For film forming purposes, it is desirable that the VA content of the EVA be from about 3% to about 25% as when an EVA has a higher VA content the EVA behaves more like a glue or adhesive. Ethylene alkyl acrylate copolymers (EAA) re-fers to copolymers formed from ethylene and alkyl acrylate wherein the ethylene derived units in the copolymer are present in major amounts and the alkyl acrylate derived units in the copolymer are present in minor amounts.
Thus, the term "ethylene-methyl acrylate copolymer" (EMA) refers to a co-polymer formed from ethylene and methylacrylate monomers. The term "ethylene-ethylacrylate copolymer (EAA) refers to a copolymer formed from ethylene and ethyl acrylate monomers. The term "ethylene-butyl acrylate copolymer" (EBA~ refers to a copolymer formed from ethylene and butyl acrylate monomers. Many suitable EBA's are commercially available and these have a butyl acrylate content from about 3% to about 18% by weight.

Also suitable for blending are copolymers of an alpha-olefin of the formula RHC=CH2 wherein R is H or Cl to C8 alkyl and an alpha,beta-ethylenically unsaturated carboxylic acid, and the like. Preferably, inthe RHC=CH2 copolymer of an olefin and a carboxylic acid, the olefin is ethylene and the carboxylic acid is acrylic acid or methacrylic acid.
Materials, which are the copolymer of an alpha-olefin having the formula RHC=CH2 wherein R is H or Cl to C8 aIkyl and an alpha,beta-ethylenically unsaturated carboxylic acid, representatively may be one of the Nucrel (TM) polymers supplied by du Pont or may be one of the Primacor (TM) polymers, supplied by Dow Chemical Company, Midland, Michigan. These are produced by the copolymerization of ethylene and a carboxylic acid comonomer therefor such as acrylic acid or methacrylic acid. Also, the copolymer of an alpha-olefin having the formula RHC=CH2 wherein R is H or Cl to C8 aIkyl and analpha,beta-ethylenically unsaturated carboxylic acid may be metal salt 1303~90 neutralized such as with sodium, Na. Thus, the copolymer may be an i~nomer.
Representatively, such an ionomeric material is commercially available as Surlyn (IM) from the E. I. du Pont de Nemours Company of Wilmington, Delaware, and is described in detail in U. S. Patent 3,355,319 and U. S.
Patent 3,845,163.

In the preferred embodiment, the film is antistatic or static dissipative, and may be employed for skin packaging of electrostatic sen-sitive items such as circuit boards. Nevertheless, this e~odiment of the film is also suitable for skin packaging of other products that do not need antistatic protecti , such as pork, red meat, cartons of cottage cheese, boxed toys wherein one side of the box is open for viewing the toy through the plastic filn skin package, and the like.

In the antistatic embodiment, the polymer contains less than about 20 percent by weight, more preferably less than about 15 percent by weight, of e or more antistatic agents. The agent(s) will generally increase the c ductivity of the polymer (polymers are typically excellent insulators) by an order of magnitude up to several orders of magnitude. There is no particular method required for incorporating an agent into the polymer, and any of the well-known solvent '~et" blending, melt blending, or dry blending methods may be employed.

This antistatic embodiment may be exhibited by the ability of the polymeric film ccr~taining the agent to promote static charge decay, i.e. to dissipate a static charge. The film of polymer c taining the agent is able to dissipate 99% of an applied static charge of ~5000 volts direct current in a short amount of time, i.e. less than 20, more preferably less than 5, most preferably less than 2 seconds (2000 milliseconds).

The Department of Defense (DOD) and the Electronics Industry Association (EIA~ each have their ~wn standards on surface resistivity of a material in ohms/square as follows:

~303~90 SURFAOE RESISTIVITY RANOES

Static Insulative Antistatic Dissipative Conductive DOD Greater Than 1014 1014 to 109 109 to 105 Less Than 105 EIA Greater Than 1013 1013 to 105 Less Than 105 As can be seen, there are two main differences. Cne is that EIA~defines insulative as above about 1013 ohms/square, whereas DOD defines insulative as above about 1014 ohms/square. The other difference is that EIA has one range of about 1013 to about 105 ohms/square as antistatic, which results in antistatic being synonymous with static dissipative. Cn the other hand, DOD
divides this into two separate ranges of about 1014 to about 109 ohms/square for antistatic and about 109 to about 105 ohms/square for static dissipa-tive. Frequently the literature, especially older literature, equates antistatic with static dissipative in discussions about static electricity.

Thus, the term "antistatic" as used herein describes material having a surface resistivity in the range of about 109 to 1014 ohms/square (Department of Defense standard) and/or a material which can dissipate 99~
of an applied static charge of ~ 5000 volts direct current in a short amount of time, preferably less than about 20 seconds, more preferably less than about 5 seconds, st preferably less than about 2 seconds (Federal Test Method Standard 101C, Method 4046.1, "Electrostatic Properties of Materials"), and/or a material having a surface resistivity in the range of about 105 to 1013 ohms/square (an alternative standard of the Electronics Industry Association).

The antistatic agents useful in the preferred embodiment of the present invention may be selected from (a) one or more fatty acid esters of polyhydroxy alcohols, (b) one or more polyalkoxylated co~,pounds (i.e. poly-ethers) such as polyethylene oxides, polypropylene oxides, polybutylene oxides, polytetramethylene oxides, the reaction products of polyalkoxylates with long chain acids, the reaction products of polyalkoxylates with long chain alcohols, the reaction products of polyalkoxylates with long chain acid esters of polyhydroxyl alcohols (for instance polyalkoxylate reaction i303790 products of long chain acids, of fatty glycols, of fatty sorbitols, of fatty sorbitans, and of fatty alcohols), or a mixture thereof, or a mixture of (a) and (b). Suitable long chains in either (a) or (b) are desirably from about C8 to about C20 or higher. The polyether chains in the suitable poly-alkoxylated compounds are of the formula (-OCxH2x-)n wherein x is from 2 to about 8, wherein the alkyl group is straight or branched, and wherein n is fram 2 to about 1000. Each agent will work by itself in a polymeric com-position, as such antistatic clpositions exhibit excellent static decay times; however, the combin,ation of agents (a) and (b) in a polymeric com-position is more desirable as these antistatic conpositions display evenshorter static decay times. Desirable fatty acid ester substituted poly-hydroxy alcohols include, but are not limited to, the polyhydroxy alcohols selected from the C2 to C6 alcohols, such as ethylene glycol, 1,3-propylene glycol, 1,2-propylene glycol, 1,2-butanediol, meso-2,3-butanediol, 1,4-butanediol, pinacol, pentaerythritol, 1,2,3,4,5-pentanepentol, sorbitan, or sorbitol, which polyhydroxy alcohol has been substituted with one or more fatty acid ester groups. A very desirable fatty acid ester substituted polyhydroxy alcohol is glycerol monostearate (GMS). A desirable polyether is polyethylene oxide (PEO), such as that sold by Union Carbide under the trade name Polyox, or is polytetramethylene oxide, such as that sold by du Pont under the trade name Terathane. A very desirable poly-alkoxylate of a fatty alcohol is a polyethoxylated cetyl alcohol (PECA~, as represented by the formula C16H33-O(-C2H4-O-)nH wherein n is from 2 to about 50. A very desirable antistatic film comprising linear ethylene/alpha-olefin copolymer contains GMS, PEO, and PECA.

Advantageously, the admixture of polymer and antistatic agent alsoincludes a small amount of about 10% by weight or less, more desirably about 7% by weight or less of an antiblock, to help alleviate any tactile tackiness. A suitable antiblock is the siloid present in EPE 8160 supplied by Teknor Apex.

Manufacturing of films may be accomplished as follows. The film may be formed fr~ non-orientable material or, if formed from an orientable (i.e. heat-shrinkable) material may be formed from a tube by using a "trapped bubble" technique c~mmonly known as the "hot blown" technique. In forming a hot blown film, the tube is first stretched by a hot blown bubble essentially immediately after extrusion while the tube is still at an elevated temperature above the orientation temperature range of the material. l`hereafter, the film is cooled, by well-kno~n methods. Those of skill in the art are well familiar with this process and the fact that the resulting film has substantially unoriented characteristics. Other methods for forming unoriented films are well known. Exemplary, are the planar methods of slot die extrusion or cast extrusion which, likewise, are well knuwn to those in the art. If an oriented, i.e. heat-shrinkable, film is desired, the manufacture may be generally accomplished by extrusion (single layer films) or coextrusion (multi-layer films) of thermoplastic resinous materials which have been heated to or above their flow or melting point from an extrusion or coextrusion die in, for example, either tubular or planar (sheet) form, followed by a post extrusion cooling. The stretching for orientation may be conducted at s~me point during the cool dcwn while the film is still hot and at a temperature within its orientation temperature range, followed by c~mpleting the cooling. Alternatively, after the post extrusion cooling, the relatively thick "tape" extrudate is then reheated to a temperature within its orientation temperature range and stretched, to orient or align the crystallites and/or molecules of the material and then cooled down. An "oriented" or "heat shrinkable" material is defined herein as a material which, when heated to an appropriate temperature above room temperature (for example 96C), will have a free shrink of about 5% or greater in at least one linear direction.

Many other process variations for forming films are well known to those in the art. For example, conventional thermoforming or laminating techniques may be employed. For instance, multiple substrate layers may be first coextruded via a blown bubble tube with additional layers thereafter being extrusion coated or laminated thereon, or two multi-layer tubes may be co~xtruded with one of the tubes thereafter being extrusion coated or laminated onto the other.

As used herein the term "extrusion" or the term "extruding" is intended to include extrusion, coextrusion, extrusion coating, or combinations thereof, whether by tubular methods, planar methods, or combinations thereof.

,. 1,,~

If desired, the film of the invention may contain a barrier layer.
The barrier layer may be composed of a layer comprising vinylidene chloride copolymer (saran), or c~mposed of a layer comprising hydrolyzed ethylene-vinyl acetate copolymer (EVOH), preferably hydrolyzed to at least about 50%, most preferably to greater than about 99%, or composed of both a layer comprising vinylidene chloride copolymer and a layer comprising EVOH. When the barrier layer is ccmposed of a layer comprising EVOH, the le percent of vinyl acetate prior to hydrolysis should be at least about 29%, since for lesser amounts the effectiveness of the hydrolyzed copolymer as a barrier to fluids such as gas is substantially diminished. It is further preferred that the barrier copolymer have a melt flow being generally compatible with that of the other components of the multi-layer film, preferably in the range of about 3-10 (melt flow being determLned generally in accordance with ASTM D1238). The gas of main concern is oxygen and transmission is considered to be sufficiently low, i.e. the barrier material is relatively gas impermeable, when the transmission rate for the barrier material is be-low 70 cc/m2/mil thickness/24 hours/atms, as measured according to the pro-cedures of ASTM Method D-1434. EVOH can be advantageously utilized in the film of the invention since irradiative high energy electron treatment of the fully coextruded film does not degrade a~ EVOH barrier layer, as could be the case of a vinylidene chloride copolymer barrier layer, as is further discussed below. 'rhis gas "impermeability" of barrier polymers such as Saran or EVOH as described in this paragraph is intended only to be a re-ference to barrier polymers. It is not intended to be a reference to the gas "impervious" characteristic of one kind of support used in skin packag-ing as described above, although in some skin packaging applications it may be desirable to employ a barrier polymeric film as the support.

Irradiation is not necessary, as very suitable films exhibiting an excellent deep draw and a high draw ratio can be obtained without irradiation. Irradiative cross-linking, if desired, may be accomplished by the use of high energy electrons, ultra-violet rays, X-rays, ga~ma rays, beta particles, etc. Preferably, electrons are e~lployed up to about 20 megarads (MR) dosage. 'rhe irradiation source can be any electron beam generator operating in a range of about 150 kilovolts to about 6 megavolts with a power output capable of supplying the desired dosage. 'rhe voltage can be adjusted to appropriate levels which may be for example 1,000,000 or ` i;~03790 2,000,000 or 3,000,000 or 6,000,000 or higher or lower. Many other apparatus for irradiating films are knc~n to those of skill in the art. The irradiation is usually carried out at a dosage between about 1 MR and about 20 MR, with a preferred dosage range of about 2 MR to about 12 MR.
Irradiation can be carried out conveniently at room temperature, although higher and lower temperatures, for example, 0C to 60C may be employed.

Furthermore, those of skill in the art generally recognize that irradiation with high energy electrons is generally harmful to saran barrier layer compositions, as irradiation may degrade and discolor saran, making it turn brownish. Thus, if full coextrusion followed by high energy electron irradiation of the multi-layer structure is carried out on a film having a barrier layer containing a saran layer, the irradiation should be done at low levels with care. Alternatively, this situation may be avoided by using extrusion coating. Accordingly, by means of extrusion coating, one may first extrude or coextrude a first layer or layers, subject that layer or layers to high energy electron irradiation and thereafter extrusion coat the saran barrier layer and, for that matter, simultaneously or sequentially extrusion coat other later layers (which may or may not have been irradiated) onto the outer surface of the extruded previously irradiated tube. This sequence allaws for the high energy electron irradiative treat-ment of the first and later layer or layers without subjecting the saran barrier layer to the harmful discoloration effects thereof.

Cross-linking of the polymers may also be accomplished chemically through utilization of chemical cross-linking agents, as is well kncwn to those of skill in the art. For instance, cross-linking agents, such as organic peroxides or dialdehydes, have been used to cross-link polyethylene polymers and copolymers. A general discussion of chemical cross-linking can be found at pages 331 to 414 of volume 4 of the Encyclopedia of Polymer Science and Technology, Plastics, Resins, Rubbers, Fibers published by John Wiley ~ Sons, Inc. and copyrighted in 1966.

DETAILED DESCRIPTION OF THE DRA~INGS

Referring to FIG. l, a schematic view of an object 5 is shcwn skin packaged to a support 3. The object is of rectangular cross-section in the direction horizontal to the support. The support 3 is perforated Surlyn-coated cardboard ~not shown). The film 4 goes fron the top 2 of the object5, dcwn to wherein portion 1 of the film covers the support 3.

Referring to FIG. 2, a schematic view of a pencil 10 having sharpened point 9 is shown skin packaged with film 7 to support 6 with the point 9 in the direction away from support 6 and the eraser end adjacent support 6.
The support 6 is Surlyn coated cardboard (not shcwn). Also shown is some webbing 8 of film 7 about 2/3 of the way down from point 9.

EXAMPLES

The follawing Examples illustrate the preferred embodiments of the invention. It is not intended to limit the invention thereby.

All percentages indicated in the Examples are percentages by weight, except the amount of Polyox was so small that it is indicated in parts per million (ppm).

The following materials were employed in the Examples;

Trycol (TM) 5984 is a polyethoxylated cetyl alcohol (PECA) supplied by Emery Industries.

Food grade (GMS) glyceryl monostearate CPH-53-N was supplied by C.
P. Hall.

- Alathon~F-3445 is an EVA having about 3.5~ vinyl acetate. It was supplied by du Pont.

~ D~

i~03'790 D~w XU 61512.08L is a VLDPE supplied by Dow. lhe cononuner is octene; the melt index is 0.80, and the density is 0.905.

Dowlex (TM) 2045.04 is a linear low density polyethylene supplied by Dow Chemical Company, Midland, Michigan. It has a density of 0.920 i 0.002; the co nomer is octene; and the melt index is 1.1. Hereinafter, this is referred to as LLDPE.04 for brevity.

Dowlex (TM) 2045.03 is a linear low density polyethylene supplied by Dow Chemical Company, Midland, Michigan. It has a density of 0.920;
the comonomer is octene; and the melt index is 1.1. Hereinafter, this is referred to as LLDPE.03 for brevity.

Chemplex 3404 is a LDPE supplied by Chemplex Company, Rolling Meadows, Illinois.

EPE 8160 clear concentrate antiblock is a micron sized silica which is a blend by weight of 90% LDPE (Dow Resin 722) with 10% Syloid 378. The syloid is an infrared opaquefier supplied by Teknor Apex.

Polyox (TM) is a polyethylene oxide (PEO) sold by Union Carbide.

EXA~PLE I

Using the method of slot die extrusion with a Pacemaker 3.5 inch (8.9 cm) slot die extruder supplied by National Rubber Manufacturers, a 20 mil (0.51 mm) thick film was made having the following composition:

, I ~, 1303~790 IABLE I

Ingredient (% PERCE~IAOES
LLDPE.04 98.5) PECA. 1.0) 90%
GMS 0.5) ~ 100%
PEO 200 ppm) ~PE 8160 10%
Next, using skin packing machines supplied by AmPak, the follownr.g items were skin paclcaged with the film using a Surlyn-coated perforated cardboard backing board as a support:

a) wooden block of 2-7/& inches X 5 inches X 9 inches with the 9 inch length vertical to the cardboard; draw ratio was about 3.1:1;

b) lead brick of 2 inches X 4 inches X 8 inches with the 2 inch thickness vertical to the cardboard; draw ratio was about 0.5:1;

c) cylindrical soda can of 3-5/8 inches diameter X 4-3/4 inches height with the 4-3/4 inch height vertical to the cardboard; draw ratio was about 2.3:1;

d) circuit board of 5 inches wide X < inch thick X 6 inches long with the < inch thickness vertical to the board; draw ratio was about 12:1;

e) capacitor of 2-< inches diameter X 4> inches height with the 4>
inch 'neight vertical to the cardboard and the capacitor had < inch tall multiple pointed pin connectors pointing in the vertical direction; draw ratio was about 1.7:1;

f) pointed wooden stick of 1/8 inch diameter X 8< inches height with the 8< inches height vertical to the cardboard; draw ratio was about 64:1;

g) pocket knife of about 3/16 inch X 6-3/4 inches height with the 6-3/4 inches height vertical to the cardboard and the exposed blade pointed up; draw ratio was about 36:1;

h) inductor can of 2< inches X 2 inches X 2 inches with a 2 inch thickness vertical to the cardboard and the can had pins pointing up; draw ratio was about 1:1.

For all of these, the fi~m was observed during skin packaging to draw well over sharp points and corners, exhibiting excellent deep draw strength and elongation. The film did not split during the skin packaging. This is particularly noted for the pointed wooden stick which exhibited an extrenely high draw ratio of about 64:1. The packaged lead brick was turned over and held upside down several times. Although the brick weighed about 26 pounds 10 ounces (about 12.1 kg), the fi~m immobilized the brick firmly, exhibited excellent strength in packaging a heavy object, and did not rip.

EXAMPLE II

The fi~n of Example I above was tested for its antistatic pro-perty. The ability of each sample to dissipate a static charge was measured using the procedure described in Federal Test Method Standard 101C, Method 4046.1, "Electro-static Properties of Materials" (change notice dated October 8, 1982) on a static decay meter. Such meters are commercially available, such as the 406C static decay meter supplied by Electrotech Systems, Inc. Except where differences are indicated, samples were equilibrated at about room temperature at less than about 15% relative humidity for about 24 hours. After equilibration, each was placed in a static decay meter at 72-73 F. ~22-23 C) and charged to ~5000 VDC (volts direct current) at less than about 15% relative humidity. The time for 99%
of the charge to dissipate was then measured.

~303790 TABLE II

Sample Decay Time (milliseconds~
Fi~m by itself 725 Film skin packaged around wooden block 1585*
*Decay time was tested on the side of the package from the tall axis EXoMPLE III

Several 4-mil thick monolayer films were extruded by the hot blown method as described above. These films were as follows:

TABLE IIIA

10 FILM POLYMER EPE 8160 IRRAD (MR) Al VLDPE 90% 10% None A2 VLDPE 90% 10% 6 A3 VLDPE 100% None A4 VLDPE 100% 6 15 Bl T.T.nPE.03 90% 10% None B2 LLDPE.03 90% 10% 6 B3 LLDPE.03 100% None B4 T~T~npE~o3 100% 6 Cl LDPE 90% 10% None 20 C2 LDPE 90% 10% 6 C3 LDPE 100% None C4 LDPE 100% 6 Dl EVA 90% 10% None D2 EVA 90% 10% 6 25 D3 EVA 100% None D4 EVA:100% 6 Next, using an AmPak skin-packaging machine, various items were skin packaged. For draw ratios up to and including 7:1, stacks of cubic blocks were used; for draw ratios of 10:1 and above, rigid plastic cylinders were used. Ordinary children's wooden cubic blocks of about 1 inch x 1 inch x 1 inch (about 2.5 cm x 2.5 cm x 2.5 cm) were skin packaged with the various films to Surlyn-coated cardboard. Blocks were chosen be-cause vertical stacking readily correlated to approximate draw ratio, i.e. a stack of 5 blocks was about a 5:1 draw ratio. At a ratio of 10:1, however, ,he AmPak machine did not have enough head room to continue with the blocks, so the rigid plastic cylinders were used. Deep draw for the particular draw ratio was rated as poor (the film split), good (the film did not split but did not draw tightly to the base) or excellent (the film drew tightly to the base and did not split). Adhesion was judged by relative cardboard fiber binding involvement of the Surlyn coated cardboard to the film when the film was pulled off the Surlyn-coated cardboard. The results are summarized in Table IIIB below:

TABLE IIIB

DEEP DRAW ADHESION TO
D~ PERFORMANOE SURLYN-COATED

Al 3:1 x NT*
4:1 x NT
5:1 x Sealed with few fibers bourld 7:1 x NT
10:1 x Sealed with few fibers bound 12:1 x Sealed with few fibers bound 14:1 x Sealed with few fibers bound 16:1 x Sealed with few fibers bound A2 3:1 x NT
4:1 x NT
5:1 x Poor Sealing ~ C~

1303'790 DEEP DRAW ADHESION TO
DEEP PERFORMAN OE SURLYN-COATED
FrLM DRAW RATIOPOOR GOOD EXCELLENT CA~DBOARD PERFORMAN OE
A3 3:1 x N~
4-1 x NT
5.1 x Sealed with few fibers bound 7:1 x NT
10:1 x Sealed with few fibers bound 12-1 x Sealed with few fibers bound 14:1 x Sealed with few fibers bound 16:1 x Sealed with few fibers bound A4 3:1 x NT
4:1 x NT
5:1 x Poor Sealing 20 Bl 3:1 x NT
4-1 x NT
5-1 x Poor with few fibers bound 7:1 x NT
10:1 x Excellent with fibers bound 12:1 x Excellent with fibers bound 14:1 x Excellent with fibers bound 16:1 x Excellent with fibers bound - B2 3:1 x NT
4:1 x NT
5:1 x Very good with fibers bound B3 3:1 x NT
4:1 x NT
5:1 x Sealed with same fibers bound 7:1 x NT
10:1 x Excellent with fibers bound 12:1 x Excellent with fibers bound 14:1 x Excellent with fibers bound 16:1 x Excellent with fibers bound 404/870608/4/~1 13()3790 DEEP DRAW ADHESION TO
DEEP PERFORMAN OE SUKLYN-COATED
FrLM DRAW RATIO POOR GOOD EX OE LLENT CARDBOARD PERFORMAN OE
B4 3:1 x NT
4:1 x NT
5:1 x Sealed with so~e fibers bound Comparison Cl 3:1 x NT
4-1 x NT
5-1 x Sealed with some fibers bound 7:1 x NT
10:1 x Poor sealing 12:1 x Poor sealing 14:1 x Poor sealing 16:1 x Poor sealing Ccmparison C2 3:1 x NT
~:1 x NT
5:1 x Very good with fibers bound 6:1 x NT
7:1 x NT
Cc~parison C3 3:1 x NT
4-1 x NT
5-1 x Poor with few fibers bound 7:1 x NT
10:1 x Poor sealing 12:1 x Poor sealing 14:1 x Poor sealing 16:1 x Poor sealing Comparison C4 3:1 x NT
4-1 x NT
5-1 x Sealed with some fibers bound 6:1 x NT
7:1 x NT
Comparison Dl 3:1 x NT
4-1 x NT
5-1 x Poor with few fibers bound -- ~ 2 -~303'79(~

DEEP DRAW ADHESION TO
DEEP PERFORMANCE SURLYN-COATED
FIL~I DRAW RATIO POOR GOOD EXCELLENT C~RDBOARD PERFORMANCE
Comparison 5 D2 3:1 x NT
4:1 x NT
5:1 x Poor with few fibers bound 7:1 x NT
10 Comparison D3 3:1 x NT
4:1 x NT
5:1 x Poor with few fibers bound 15 Comparison D4 3:1 x NT
4:1 x NT
5:1 x Poor with few fibers bound 7:1 x NT
''NT = Not Tested As can be seen from Table IIIB, the deep draw ratio was excellent for VLDPE, LLDPE and LDPE (film samples Al through C4), but only good or poor for EVA (fi~m samples Dl through D4). Thus, the deep draw of the linear ethylene/alpha-olefin films of the invention was superior to that of EVA. Also, irradiation im~roved the adhesion to the Surlyn-coated cardboard for LLDPE, LDPE, and EVA.

Next, it was illustrated that the linear ethylene/alpha-olephin films of invention were superior to conventional LDPE films. With the VLDPE, TTnpE and LDPE (but not EVA) fi~ms, pencils (like that illustrated in FIG. 2 but n sharpened) were skin packaged in the vertical direction. The pencils had a diameter of about 0.29 inch (about 0.74 cm) and a height of about 7.5 inches (19.1 cm). The blunt, unsharpened end of the pencils was away from the cardboard and the eraser end was adjacent the cardboard.
Webbing occurred about half way down the pencils. The results are summarized in Table IIIC below:

TABLE IIIC

D~ DRAW ADHESION TO
DEEP DRAW PERFORMANOE SURLYN-COATED
FIIM RATIO POOR OD EXCELLENT CABDBOARD PERFORMA~OE

5 Al 26:1 x Tacky but no fibers A2* 26:1 x Some fiber involvement A3 26:1 x Tacky but no fibers A4* 26:1 x Some fibers and card-board delamination 10 Bl 26:1 x Very modest fiber involvement B2* 26:1 x Some fiber involemment B3 26:1 x Very modest fiber involvement 15 B4* 26:1 x Some fibers and card-board delamination Clattempted 26:1 x Tacky but no fibers C2*attempted 26:1 x Some fibers and card-board delamination 20 C3attempted 26:1 x Tacky but no fibers C4*attempted 26:1 x Some fibers and card-board delamination *Irradiated at 6 MR.
All irradiated skin packaged pencils listed to an angle of about 20 to 30 from the cardboard base support. While it is not intended to be bound to any theory, it is believed this was due to the irradiation making the film so tough that it pulled the pencil instead of allowqng it to remain substantially vertical.

All the LDPE fi~m samples (Cl to C4) exhibited poor deep draw and ripped open at an attempted draw ratio of 26:1, whereas the VLDPE film samples (Al to A4) and LLDPE fllm samples (Bl to B4) exhibited excellent deep draw at a draw ratio of 26:1. Thus the deep draw of the linear ethylene/alpha-olefin films of the invention is superior to that of con-ventional LDPE.

While certain representative embodiments and details have been shown for the purpose of illustration, numerous modifications to the formulations described above can be made without departing from the in-vention disclosed.

Claims

1. A skin packaging process for packaging an electrostatically sensitive item comprising:
(a) placing the item to be packaged on a support;
(b) positioning a film above said item;
(c) heating the film;
(d) drawing a vacuum between said film and said support; and (e) drawing the film over and around the item forming a heat seal with the support;
(f) wherein said film comprises an antistatic linear ethylene/alpha-olefin copolymer film and wherein said linear ethylene/alpha-olefin copolymer is a blend with one or more antistatic agents chosen from (a) one or more fatty acid esters of polyhydroxy alcohols, (b) one or more polyalkoxylated compounds, or a mixture of (a) and (b).

2. A skin packaging process for packaging an electrostatically sensitive item comprising:
(a) placing the item to be packaged on a support;
(b) positioning a film above said item;
(c) heating the film;
(d) drawing a vacuum between said film and said support; and (e) drawing the film over and around the item forming a heat seal with the support;
(f) wherein said film comprises an antistatic linear ethylene/alpha-olefin copolymer film and wherein said linear ethylene/alpha-olefin copolymer is in blend with glycerol monostearate, polyethoxylated cetyl alcohol, and polyethylene oxide.