US3751281A - Method for preparing a dimensionally stable waxed polyethylene sheet - Google Patents

Method for preparing a dimensionally stable waxed polyethylene sheet Download PDF

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US3751281A
US3751281A US3751281DA US3751281A US 3751281 A US3751281 A US 3751281A US 3751281D A US3751281D A US 3751281DA US 3751281 A US3751281 A US 3751281A
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film
polyethylene
wax
percent
web
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J Peterson
M Shida
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Chemplex Co
Rexam Beverage Can Co
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/0427Coating with only one layer of a composition containing a polymer binder
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/048Forming gas barrier coatings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2323/04Homopolymers or copolymers of ethene
    • C08J2323/06Polyethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2491/00Characterised by the use of oils, fats or waxes; Derivatives thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers

Definitions

  • ABSTRACT This invention relates to a method for applying a wax coating to one or both sides of a polyethylene-based film which eliminates a hitherto troublesome problem of dimensional instability of the overwaxed film. More specifically, this invention provides a method for producing a waxed polyethylene film having a degree of dimensional stability heretofore not achieved.
  • the waxed sheet When prepared in accordance with the process of this invention, the waxed sheet is dimensionally stable within the limit of i2 percent even after extended periods of storage and exhibits very desirable protective properties as a packaging film.
  • the basic polyethylene film which is to be overcoated with a petroleum wax is first subjected to a surface treatment of the oxidative type which so modifies the surface layer of the film that it is more readily wet by the molten wax, which then spreads more evenly on the film surface to form a smooth overall coating of uniform thickness.
  • Any of the conventional polyolefin surface treatments may be utilized, including corona discharge, flame treatment or an oxidative chemical treatment, all being carried out in known manner and not being a part of the present invention.
  • the protective properties of the overwaxed film are, in large measure, dependent on an even distribution of the wax composition coating over the surface of the polymer film, which is generally enhanced by the surface treatment of the base film.
  • the moisture vapor transmission rate of a 1.5 mil (1 mil 0.001 inch) high density polyethylene film is in the range of 5 -l0 gm. per square meter per 24 hours. If this film is corona discharge treated and overwaxed with 4 lb. per ream (3,000 sq. ft.) of a F.
  • the moisture vapor transmission rate is reduced to between 0.5 and L0 gm/M /24 hrs., whereas a similar film overwaxed without prior corona discharge treatment will have a MVTR of between 2 and 4 gm/Ml24 hrs.
  • the data herein presented are all based on films which have been subjected to an oxidative surface treatment prior to the overwaxing operation.
  • the stretching and waxing operation is carried out on apparatus such as that shown schematically in the accompanying drawingwherein a web of polyethylene 10 is unwound from stock roll 11, led over idler rolls 12 and through a nip formed between a back-up roll 16 and an application roll 17, which latter roll is rotatably mounted with the lower portion of the roll dipping in a bath of molten wax 20 maintained at the desired waxing temperature in a wax pan 21.
  • the applicator roll preferably has an etched, engraved or knurled surface which carries sufficient molten wax from the pan 21 up into contact with the web 10 to maintain a flooded nip where the sheet passes between the two rolls l6 and 17.
  • the rolls l6 and 17 may be so arranged that the web 10 dips in the wax bath so that both sides of the web receive a coating of the wax composition.
  • the coated side (or coated sides) of the sheet may be passed over a heated metering rod or roll 22, suitably a conventional wire-wound rod or other comparable device to remove any-excess of wax and to smooth the wax film to a coating of even thickness on the web surface. If both sides of the sheet are coated, each side will be subjected to a metering operation, of course.
  • the coated sheet after passing idler roll 23 is then successively passed into contact with a tempering drum 2S maintained at a few degrees below the melting point of the wax, and then to the surface of cooling drums 27 and 28 which complete the solidification and hardening of the wax coating and f1- nally, after passage over idler roller 30, the wax coated sheet is wound into roll form on a wind-up roll 32.
  • the applicator and backup rolls 17 and 16 are provided with a first variable speed driving means, not shown, and the tempering drum 25, the cooling drums 27 and 28 and wind-up roll 32 are provided with a second variable speed driving means.
  • the tempering and cooling drums and the wind-up roll may be run, as desired, at variably higher speeds than the applicator and back-up roll, thus imparting a preselected degree of stretch to the waxed film in the critical area between the waxapplying nip and the tempering and cooling drums.
  • the film will attain a temperature above the melting point of the wax in the wax pan and it is important to the dimensional stability of the final, wax-coated film that the desired degree of stretch is applied to the film while it is heated in a temperature range between the wax melting point (usually at least 130 F.) and a maximum temperature which approaches the softening point of the polyethylene.
  • the softening temperature of polyethylene varies depending on the molecular weight and density of the film, low density polyethylene generally softening in the vicinity of about 220-230 F. while the softening point of high density polyethylene may range as high as 260 F. or slightly above.
  • the temperature of the waxing bath, the applicator roll, back-up roll and the metering roll be controlled to, first, raise the temperature of the film into the-desired temperature range and then to maintain it within this range during the waxing and stretching operations.
  • the heatedfmolten wax provides sufficient heat to achieve the abovedescribed desired result, but it is to be understood that the film may be partially preheated before its delivery to the waxing nip as, for example, by utilizing one or more of the idler rolls 12 as a preheating roll for the film.
  • wax coating required will depend on the particular protective requirements of the specific packaging situation and will also vary somewhat depending on the type and caliper of the polyethylene base film and on the particular wax composition utilized. It is to be understood that a wide variety of wax compositions based primarily on petroleum wax may be utilized. Both paraffin wax and microcrystalline petroleum wax may be used, as well as blends of either or both of these materials with such other known wax composition components as polyolefins, ethylene-vinyl acetate co-polymers, natural and synthetic resins and the like.
  • Typical wax compositions suitable for the present invention would include paraffin wax containing from 1 percent to 50 percent ofethylene vinyl acetate co-polymer, blends of paraffin wax with minor percentages of microcrystalline wax and/or polyethylene, polyisobutylene, rosin, natural and synthetic rubber, hydrogenated rosin esters and the like.
  • paraffin wax containing from 1 percent to 50 percent ofethylene vinyl acetate co-polymer, blends of paraffin wax with minor percentages of microcrystalline wax and/or polyethylene, polyisobutylene, rosin, natural and synthetic rubber, hydrogenated rosin esters and the like.
  • Generally, between 1 lb. of wax composition and about 10 lbs. of wax composition per ream (3,000 sq. ft.) of polyethylene applied to either one or both surfaces of the web is quite adequate to provide the degree of protection desired in the packaging film. Greater amounts of the coating could be applied but are less economical and lesser amounts are generally ineffective.
  • a preferred range of coating weight is from 3 to 6 lbs.
  • the following table presents data comparing the water vapor transmission rate of an unwaxed high density polyehtylene film (1.5 mil in caliper) made from Chemplex 6,108 polyethylene resin with the MVTR of a similar film overwaxed with 4.8 lbs/ream of l35l40 F. melting point paraffin and with a similar waxed film which had been stretched to the extent of 12 percent during the waxing operation in accord with the process of this invention as hereinbefore described.
  • Moisture vapor transmission rate was determined on all samples according to the procedure setforth in TAPPl standard method number T-464-m-45.
  • the waxed films were conditioned for eight hours at 120 F. prior to conducting the MVTR tests. Values of MVTR are reported in grams per square meter per 24 hours.
  • HDPE high density polyethylene
  • LDPE low density polyethylene
  • PP polypropylene
  • Sample C is high density polyethylene film obtainable from Allied Chemical Corporation, Plastic Film Department, Chicago, Ill.
  • Sample D is a blown high density polyethylene film prepared from pelletized resin designated Chemplex 6,108 and obtainable from Chemplex, Rolling Meadows, lll.
  • Samples E and F are high density cast polyethylene films prepared from pelletized resins designated by the numbers 7,140 and 7,150, respectively, which are available from E. I. duPont de Nemours & Co., Electrochemicals Department, Chicago, 111.
  • Sample G a cast high density polyethylene film, was prepared from pelletized resin designated Amoco 650- 134, which is obtainable from Amoco Chemical Corporation, Chicago, 111.
  • Sample H a cast low density polyethylene film, was prepared from pelletized low density polyethylene, designated as USL, N.A. 222, obtained from U. S. Industrial Chemicals Company, Oak Brook, 111.
  • Sample A is a high density polyethylene film designated as Philjo 606W.
  • Sample B is a high density po nated as Philjo 670W.
  • Sample 1 is a polypropylene fil 410.
  • Samples A, B an Joanna, Division of Ladd, Illinois.
  • lyethylene film desigm designated as Philjo d l are obtainable from Phillips Joanna Western Mill Company of ures on the percentage elongation of the waxed film at the end of the test period being 8 percent, 8.5 percent and 9.6 percent, respectively.
  • the degree to which a given polyethylene film must be stretched during the waxing operation in order to achieve the maximum degree of dimensional stability during storage and use of the waxed film is dependent on a number of factors, including the type and degree of crystallinity of the film, the temperature which the film attains during the waxing and stretching operation and the length of time of exposure of the film to the molten wax before the waxed film is cooled sufficiently to solidify the wax.
  • the film is heated to a temperature above 130 F., in which case the degree of stretch which must be imparted to the film during waxing to achieve satisfactory dimensional stability will seldom exceed 15 percent, and may even be as little as 6-8 percent, as will be discussed hereinafter.
  • Variation of the temperature to which the film is heated between the limits of 130 F. and about 210 F. has a relatively small effect on the amount of stretching required for dimensional stability of the waxed film. It has been found, however, that the length of time of contact of molten wax with the film during the waxing and stretching operations has a profound effect on the degree of stretch which must be imparted to the polyethylene film to achieve optimum results.
  • the waxed web need be stretched only by between percent and 9 percent while the wax is molten in order to achieve optimum dimensional stability, so that the voverwaxed sheet will change its dimensions by less than 2 percent even under extended storage under summer warehousing conditions.
  • the time required for the flooding of the polyolefin web with molten wax, the metering off of excess wax, the stretching of the waxed film and finally the chilling of the molten wax into the solid state may be only a fraction of a second. Under these conditions, it has been found that the polyolefin web must be stretched as much as to 18 percent during the waxing operation in order to achieve a dimensional stability of the product within the desired ranges.
  • melting point include maintaining the wax bath temperature at 215-220 F., flooding the web with wax at 400-450 feet per minute, metering off the excess wax with a conventional wire wound rod to leave 4.5 lbs. of wax on the web, and stretching the web during the waxing operation as hereinbefore described by the amount of 12-15 percent.
  • the resulting sheet has excellent dimensional stability and very low water vapor permeability. It is a superior sheet for use as a cereal inner wrap.
  • a method for obtaining a substantially dimensionally stable, waxed polyethylene sheet which comprises:
  • a method for obtaining a dimensionally stable wax-coated polyethylene web suitable for use in highspeed packaging operations which comprises applying a molten petroleum wax composition to at least one surface of a polyethylene web having a thickness of between 0.0005 in. and 0.005 in., maintaining said wax coating in a molten state and said polyethylene web at a temperature between about 130 F. and the softening temperature of the polyethylene while mechanically stretching said coated polyethylene web in a machine direction by an amount between about 5 percent and 20 percent, and subsequently chilling said coated and stretched web to complete solidification of said wax composition coating.

Abstract

This invention relates to a method for applying a wax coating to one or both sides of a polyethylene-based film which eliminates a hitherto troublesome problem of dimensional instability of the overwaxed film. More specifically, this invention provides a method for producing a waxed polyethylene film having a degree of dimensional stability heretofore not achieved.

Description

United $13168 Patent 1 1 Peterson et al.
Ml-'.'|'ll()l) FOR PREPARING A IHMI'INSIUNALLY STABLE WAXI II) POLY ETHYLENE SHEET Inventors: James Thomas Peterson, Oshkosh,
Wis.; Mitsuzo Shida, Barrington, 111.
Assignees: American Can Company,
Greenwich, Conn.", by said Peterson; Chemplex Company, Rolling Meadows, [11. by said Shida, part interest to each Filed: Feb. 17, 1972 Appl. No.: 227,192
US. Cl. 117/7, ll7/l38.8 E, 117/168,
264/134, 264/136, 264/288 Int. Cl. B056 3/107 Field of Search ..264/134-137,
210 R, 288489, 95; 117/7. 6,138.8 E, a 168; 156/229, 244; 118/33 References Cited 7 UNITED STATES PATENTS Taylor 264/289 1 1 Aug. 7, 1973 2,627,038 2/1953 A1105 c1111 264/134 2,880,057 3/195) Cuculo 264/210 R 3,068,516 12/1962 Hol'cr 264/134 3,140,957 7/1964 Tanu be et a1. 117/6 3,504,075 3/1970 willia'ms et 81.. 264/175 3,506,751 4/1970 Lurie 264/134 3,565,985 2/1971 Schrenk et al 264/95 Primary ExaminerJay H. Woo
Ai'tohi i iobertl AhberflflrriesA. Momma, Jr.. et al. I
[57] ABSTRACT This invention relates to a method for applying a wax coating to one or both sides of a polyethylene-based film which eliminates a hitherto troublesome problem of dimensional instability of the overwaxed film. More specifically, this invention provides a method for producing a waxed polyethylene film having a degree of dimensional stability heretofore not achieved.
7 Claims, 1 Drawing Figure PATENTEU A113 7 3. 751 281 METHOD FOR PREPARING A DIMENSIONALLY STABLE WAXED POLYETHYLENE SHEET BACKGROUND OF THE INVENTION Polyethylene film bearing a superficial coating of a petroleum wax composition possesses excellent protective properties for a number of packaging applications, and is of particular value as an innerwrap sheet for the packaging of a variety of cereals and crackers. Unfortunately, the waxed polyethylene sheet material heretofore produced exhibited the unusual and vexatious property of growth or elongation in both directions of the sheet when stored under summer warehousing conditions for a period of time in roll form after the waxing operations were completed. The extent of elongation of the web was often sufficient to cause it to separate from the core of the stock roll and the resultant distortion of the roll stock made the web unsatisfactory for use on any automated food packing machinery.' Growth or elongation of the waxed film often amounted to as much as 0.5 to 1.0 inches per foot of length and width of the web, or from about 4 percent to more than 8 percent.
The elongation which occurs upon storage of a waxed polyethylene film is relatively slow at room temperature (7075 F.) but the rate of elongation increases rapidly as the storage temperature is increased. Warehousing of the waxed film during summer months in which the temperature of normal storage areas may reach levels in the range of l-l30 F. has hitherto been impossible due to the dimensional instability of such films when subjected to even moderately elevated temperatures of storage. It has been established that a waxed film which exhibits a dimensional change of more than 2-3 percent during storage will prove unsatisfactory for use on the high speed packaging machinery commonly used in a variety of packaging applications. It is therefore imperative for commercial acceptability that the elongation of the sheet be kept well within the above limits even when subjected to storage in warehouses which may reach summer temperatures in the range of l00130 F., and preferably the dimensional change should not exceed 1.5 percent under such conditions.
It is an object of this invention to make it possible to produce an overwaxed, polyethylene-based web which is dimensionally stable during storage and use in packaging applications.
It is a further object to produce an overwaxed polyethylene web of low water vapor permeability which is satisfactory for packaging of cereals, crackers and similar food items subject to degradation in the presence of atmospheric moisture, which web may be stored without substantial dimensional variation, even under conditions of moderately elevated temperatures, and utilized in the packaging of foodstuffs on high-speed packaging machinery.
Further objects will become apparent from a perusal of the following specification taken in connection with the accompanying drawing and attached claims.
SUMMARY OF THE INVENTION It has now been found that growth or elongation of a waxed, polyethylene-base film while stored in roll form at temperatures up to l20-l F. may be eliminated or reduced to a negligible level by a unique waxing procedure whereby the polyethylene web is submitted to tension stresses during and immediately after the application of molten wax, sufficient to stretch the film by a controlled amount in the range of 520 percent of its original length. The required degree of stretch is impressed on the sheet immediately subsequent to the actual application of molten wax, the coated sheet is cooled to solidify the wax while the sheet is maintained in the stretched state and the coated web is formed into a roll and stored for use in packaging operations. When prepared in accordance with the process of this invention, the waxed sheet is dimensionally stable within the limit of i2 percent even after extended periods of storage and exhibits very desirable protective properties as a packaging film. Preferably, the basic polyethylene film which is to be overcoated with a petroleum wax is first subjected to a surface treatment of the oxidative type which so modifies the surface layer of the film that it is more readily wet by the molten wax, which then spreads more evenly on the film surface to form a smooth overall coating of uniform thickness. Any of the conventional polyolefin surface treatments may be utilized, including corona discharge, flame treatment or an oxidative chemical treatment, all being carried out in known manner and not being a part of the present invention. The protective properties of the overwaxed film are, in large measure, dependent on an even distribution of the wax composition coating over the surface of the polymer film, which is generally enhanced by the surface treatment of the base film. For example, the moisture vapor transmission rate of a 1.5 mil (1 mil 0.001 inch) high density polyethylene film is in the range of 5 -l0 gm. per square meter per 24 hours. If this film is corona discharge treated and overwaxed with 4 lb. per ream (3,000 sq. ft.) of a F. melting point paraffin wax, the moisture vapor transmission rate (MVTR) is reduced to between 0.5 and L0 gm/M /24 hrs., whereas a similar film overwaxed without prior corona discharge treatment will have a MVTR of between 2 and 4 gm/Ml24 hrs. For this reason, the data herein presented are all based on films which have been subjected to an oxidative surface treatment prior to the overwaxing operation.
DESCRIPTION OF THE DRAWINGS In the preferred embodiment of this invention, the stretching and waxing operation is carried out on apparatus such as that shown schematically in the accompanying drawingwherein a web of polyethylene 10 is unwound from stock roll 11, led over idler rolls 12 and through a nip formed between a back-up roll 16 and an application roll 17, which latter roll is rotatably mounted with the lower portion of the roll dipping in a bath of molten wax 20 maintained at the desired waxing temperature in a wax pan 21. The applicator roll preferably has an etched, engraved or knurled surface which carries sufficient molten wax from the pan 21 up into contact with the web 10 to maintain a flooded nip where the sheet passes between the two rolls l6 and 17. If desired,the rolls l6 and 17 may be so arranged that the web 10 dips in the wax bath so that both sides of the web receive a coating of the wax composition. After passing through the nip, the coated side (or coated sides) of the sheet may be passed over a heated metering rod or roll 22, suitably a conventional wire-wound rod or other comparable device to remove any-excess of wax and to smooth the wax film to a coating of even thickness on the web surface. If both sides of the sheet are coated, each side will be subjected to a metering operation, of course. The coated sheet after passing idler roll 23 is then successively passed into contact with a tempering drum 2S maintained at a few degrees below the melting point of the wax, and then to the surface of cooling drums 27 and 28 which complete the solidification and hardening of the wax coating and f1- nally, after passage over idler roller 30, the wax coated sheet is wound into roll form on a wind-up roll 32.
In order to impart a controlled degree of stretch to the polymer web during the critical portion of its travel through the waxing operation, the applicator and backup rolls 17 and 16 are provided with a first variable speed driving means, not shown, and the tempering drum 25, the cooling drums 27 and 28 and wind-up roll 32 are provided with a second variable speed driving means. With such provision, the tempering and cooling drums and the wind-up roll may be run, as desired, at variably higher speeds than the applicator and back-up roll, thus imparting a preselected degree of stretch to the waxed film in the critical area between the waxapplying nip and the tempering and cooling drums. It has been found that, in this particular phase of the operation, the film will attain a temperature above the melting point of the wax in the wax pan and it is important to the dimensional stability of the final, wax-coated film that the desired degree of stretch is applied to the film while it is heated in a temperature range between the wax melting point (usually at least 130 F.) and a maximum temperature which approaches the softening point of the polyethylene. The softening temperature of polyethylene varies depending on the molecular weight and density of the film, low density polyethylene generally softening in the vicinity of about 220-230 F. while the softening point of high density polyethylene may range as high as 260 F. or slightly above. It is therefore important that the temperature of the waxing bath, the applicator roll, back-up roll and the metering roll be controlled to, first, raise the temperature of the film into the-desired temperature range and then to maintain it within this range during the waxing and stretching operations. Generally, the heatedfmolten wax provides sufficient heat to achieve the abovedescribed desired result, but it is to be understood that the film may be partially preheated before its delivery to the waxing nip as, for example, by utilizing one or more of the idler rolls 12 as a preheating roll for the film.
DESCRIPTION OF A PREFERRED EMBODIMENT OF THE INVENTION To demonstrate, on the above-described apparatus, the effect of stretching a high density polyethylene film to varying degrees during the waxing operation, a 1.5 mil film of polyethylene blown from Chemplex 6108 high density polyethylene resin (available from Chemplex, Rolling Meadows, Ill.) was waxed with 4.8 lbs. of a l35-l40 F. melting point paraffin wax maintained at a temperature of 210 F. The film was fed to the applicator nip at 50 feet per minute, the chill roll and wind-Up rolls being operated at speeds sufficient to give the various degrees of stretch in the waxing area indicated in the following table. The resulting wax coated polyethylene films were then stored at 120 F. for eight days and tested for dimensional stability after one day, four days and eight days of such storage. The test data are recorded in the following Table I.
TABLE I ELONGATION OF WAXED POLYETHYLENE STORED AT F.
% Stretch of Elongation After Storage PE During Waxing 1 day 4 days 8 days 0% (Control) 6 7 7.7% 8% 2.4% 3.4% 3.9% 12% 0 0.4% 0.8% 14% 0.7% 1.4% 1.8% 23% -2.l% -l.4% 0.8%
The data in the above Table I clearly indicate that high density polyethylene which, during waxing at a speed of 50 feet per minute at a wax temperature of 210 F., is stretched to an extent of between 10 percent and 20 percent, yields a waxed polymer film which is well within the limits of satisfactory dimensional stability (maximum dimensional change of less than about 2 percent) for commercial utilization on high speed packaging machinery, even when the coated film is stored under rather extreme summertime warehouse temperatures. It is also quite evident that the film which was waxed without stretching (control) did not exhibit the required degree of dimensional stability.
It has previously been stated that the application of a thin coating of wax on a polyethylene film greatly reduces the water vapor transmission rate of the film and that the resulting waxed polymer film therefore has great utility in the packaging of items susceptible to the deteriorative effects of moisture.
The amount of wax coating required will depend on the particular protective requirements of the specific packaging situation and will also vary somewhat depending on the type and caliper of the polyethylene base film and on the particular wax composition utilized. It is to be understood that a wide variety of wax compositions based primarily on petroleum wax may be utilized. Both paraffin wax and microcrystalline petroleum wax may be used, as well as blends of either or both of these materials with such other known wax composition components as polyolefins, ethylene-vinyl acetate co-polymers, natural and synthetic resins and the like. Typical wax compositions suitable for the present invention would include paraffin wax containing from 1 percent to 50 percent ofethylene vinyl acetate co-polymer, blends of paraffin wax with minor percentages of microcrystalline wax and/or polyethylene, polyisobutylene, rosin, natural and synthetic rubber, hydrogenated rosin esters and the like. Generally, between 1 lb. of wax composition and about 10 lbs. of wax composition per ream (3,000 sq. ft.) of polyethylene applied to either one or both surfaces of the web is quite adequate to provide the degree of protection desired in the packaging film. Greater amounts of the coating could be applied but are less economical and lesser amounts are generally ineffective. A preferred range of coating weight is from 3 to 6 lbs. per ream of the base web.
The following table presents data comparing the water vapor transmission rate of an unwaxed high density polyehtylene film (1.5 mil in caliper) made from Chemplex 6,108 polyethylene resin with the MVTR of a similar film overwaxed with 4.8 lbs/ream of l35l40 F. melting point paraffin and with a similar waxed film which had been stretched to the extent of 12 percent during the waxing operation in accord with the process of this invention as hereinbefore described.
Moisture vapor transmission rate was determined on all samples according to the procedure setforth in TAPPl standard method number T-464-m-45.
The waxed films were conditioned for eight hours at 120 F. prior to conducting the MVTR tests. Values of MVTR are reported in grams per square meter per 24 hours.
TABLE ll MVTR OF WAXED AND UNWAXED POLYETHYLENE Film: 1.5 mil caliper High Density Polyethylene Coating: 4.8 lbs/ream of Paraffin Wax (l35-40 F.M.P.)
The data in the above table confirm the fact that overwaxing of polyethylene film produces a substantial reduction in MVTR and also demonstrate that the film waxed in accord with the process of this invention also exhibits a substantially lower MVTR than unwaxed polyethylene. It has previously been demonstrated by data in Table 1 that the stretched waxed film has a satisfactory dimensional stability, while the waxed, unstretched film does not.
The phenomenon of growth or elongation after waxing is common to both high density and low density polyethylene film and is also demonstrated, in a far lesser degree, by polypropylene film. The following table illustrates the elongation which results when unstretched polyolefin films from a variety of sources are overwaxed on one sidewith 4.0 to 4.5 lbs/ream of a paraffin wax of 135-140 F. melting point at a temperature of 170 F. and stored for periods of up to three days at temperatures from 100 F. to 120 F.
In the following table, HDPE refers to high density polyethylene, LDPE refers to low density polyethylene and PP refers to polypropylene.
TABLE 111 ELONG'ATION OF WAXED POLYOLEFINS STORED AT ELEVATED TEMPERATURE 6 Sample C is high density polyethylene film obtainable from Allied Chemical Corporation, Plastic Film Department, Chicago, Ill.
Sample D is a blown high density polyethylene film prepared from pelletized resin designated Chemplex 6,108 and obtainable from Chemplex, Rolling Meadows, lll.
Samples E and F are high density cast polyethylene films prepared from pelletized resins designated by the numbers 7,140 and 7,150, respectively, which are available from E. I. duPont de Nemours & Co., Electrochemicals Department, Chicago, 111.
Sample G, a cast high density polyethylene film, was prepared from pelletized resin designated Amoco 650- 134, which is obtainable from Amoco Chemical Corporation, Chicago, 111.
Sample H, a cast low density polyethylene film, was prepared from pelletized low density polyethylene, designated as USL, N.A. 222, obtained from U. S. Industrial Chemicals Company, Oak Brook, 111.
The data in the above table clearly indicate that unstretched waxed polyethylene film, prepared either as a blown film from a tubing type extruder or as a cast film from a slot die extruder, is subject to a substantial elongation as a result of storage at moderately elevated temperatures. Both low density polyethylene film and high density polyethylene film exhibit this peculiar characteristic in a very substantial degree, whereas polypropylene film shows only minimal elongation after waxing. Data for Sample D, above, indicate that storage temperature severely affects both the rate and extent of the elongation or growth of the waxed film, since 16 hours of storage at 120 F. results in a greater growth than hours of storage at F. Further tests have demonstrated that at 120 F. storage temperature, the waxed film elongates by 5 percent in about an hour, whereas at F., a 5 percent elongation requires about 10 hours and at 100 F., an 'equivalent elongation W x Percent Polyolefin Film Weight Storage Elongation During Caliper Temp. Storage Sample Film Type Caliper lbs/ream- Time F. Percent A HDPE Cast 2 4.0 3 days 100 4.5 B HDPE Cast 1.5 4.0 3 days 100 4.8 C HDPE Cast 4.0 3 days 100 6.2 1) HDPE Blown 1.5 4.0 60 hours 100 5.4 24 hours 110 5.6 16 hours 7.7
E HDPE Cast 2 4.0 24 hours 120 5.4 F HDPE Cast 1.5 4.0 24 hours 120 3.3 (i HDPE Cast 1.5 4.0 24 hours 120 5.7 H LDPE (,ast 1.5 4.5 3 days 110 4.3 1 PP Cast 2 4.0 3 days 100 0.3
Sample A is a high density polyethylene film designated as Philjo 606W.
Sample B is a high density po nated as Philjo 670W.
Sample 1 is a polypropylene fil 410.
Samples A, B an Joanna, Division of Ladd, Illinois.
lyethylene film desigm designated as Philjo d l are obtainable from Phillips Joanna Western Mill Company of ures on the percentage elongation of the waxed film at the end of the test period being 8 percent, 8.5 percent and 9.6 percent, respectively.
The degree to which a given polyethylene film must be stretched during the waxing operation in order to achieve the maximum degree of dimensional stability during storage and use of the waxed film is dependent on a number of factors, including the type and degree of crystallinity of the film, the temperature which the film attains during the waxing and stretching operation and the length of time of exposure of the film to the molten wax before the waxed film is cooled sufficiently to solidify the wax.
It has been determined, for example, that if a polyethylene is subjected to a waxing and stretching operation in which the film fails to reach a temperature of at least 130 F. during the waxing operation, the waxed film will show cold stretch marks and will have the desired degree of dimensional stability only if, during the waxing operation, the film is stretched by an amount in excess of 12 percent and preferably is stretched by about 20 percent. It is generally undesirable to stretch the film longitudinally to a degree approaching 20 percent, because necking in or a reduction of the width of the film tends to occur under these conditions, and this is undesirable.
It is greatly preferable to make sure that the film is heated to a temperature above 130 F., in which case the degree of stretch which must be imparted to the film during waxing to achieve satisfactory dimensional stability will seldom exceed 15 percent, and may even be as little as 6-8 percent, as will be discussed hereinafter. Variation of the temperature to which the film is heated between the limits of 130 F. and about 210 F. has a relatively small effect on the amount of stretching required for dimensional stability of the waxed film. It has been found, however, that the length of time of contact of molten wax with the film during the waxing and stretching operations has a profound effect on the degree of stretch which must be imparted to the polyethylene film to achieve optimum results. For example, if the polyethylene web is coated with a film of molten wax which is maintained in liquid state for as much as a full minute before chilling the sheet to set the wax, the waxed web need be stretched only by between percent and 9 percent while the wax is molten in order to achieve optimum dimensional stability, so that the voverwaxed sheet will change its dimensions by less than 2 percent even under extended storage under summer warehousing conditions.
By contrast, if polyethylene is waxed at commercially desirable speeds on high-speed waxing equipment such as that shown in the accompanying drawing, the time required for the flooding of the polyolefin web with molten wax, the metering off of excess wax, the stretching of the waxed film and finally the chilling of the molten wax into the solid state may be only a fraction of a second. Under these conditions, it has been found that the polyolefin web must be stretched as much as to 18 percent during the waxing operation in order to achieve a dimensional stability of the product within the desired ranges. The effect of linear speed of the waxing equipment (inversely proportional to time of contact of the polyolefin web with molten wax) is shown in the following Table IV, wherein are shown data on dimensional stability of waxed polyethylene TABLE IV EFFECT OF WAXER SPEED ON DIMENSlONAL STABILITY OF WAXED FILM Stretch imparted Change in waxed film Web Speed to film during length after storage in feet/min. waxing 10 days at 120" F. 5 8% 0.2 decrease 50 8% 4.0 increase 400 8% 7.4 increase 10% 2.8 increase 200 10% 5.8 increase 300 10% 6.4 increase 400 10% 7.2 increase 50 15% 0.4 increase 400 15% 0.9 increase From the above data it IS evident that the polyethylene web need be subjected to a higher degree of stretching to achieve dimensional stability of the waxed sheet if the rate of waxer speed is increased or, conversely, if the time of contact of the polyethylene with molten wax is decreased. As previously stated, the minimum degree of stretching of polyethylene during the waxing operation which will result in a satisfactorily dimensionally stable sheet is in the range of 5-8 percent. Since this minimum stretch can be utilized only when the wax coating is maintained in a molten state for a period of time ranging upwards of 30 seconds or so, production of waxed polyethylene sheet material on a commercial scale under these conditions would be subject to severe economic disadvantage. In actual practice, then, the operation is preferably carried out on waxing equipment which'coats the polyethylene web at several hundred feet per minute. Since this effectively reduces the dwell time of the web in contact with molten wax to a fraction of a second, it is necessary to increase the degree of stretching of the polyethylene web to compensate for the short dwell time. It has been found that, at waxing speeds up to and above 500 feet per minute, if the polyethylene web is stretched during the waxing operation to the extent of 10-18 percent, the resulting waxed sheet will show a dimensional stability well within the desired range of no more than 2% change under summer warehousing conditions. These results have been found to apply to polyethylene sheets of calipers ranging from about 0.0005 in. to about 0.005 in. For most packaging operations carried out on high-speed automatic packaging equipment, films of from about 0.001 to 0.0025 in. thickness are preferred. An optimum set of operating conditions for waxing 1.5 mil film of high density polyethylene film with a crystalline petroleum wax of l35-l40 F. melting point include maintaining the wax bath temperature at 215-220 F., flooding the web with wax at 400-450 feet per minute, metering off the excess wax with a conventional wire wound rod to leave 4.5 lbs. of wax on the web, and stretching the web during the waxing operation as hereinbefore described by the amount of 12-15 percent. The resulting sheet has excellent dimensional stability and very low water vapor permeability. It is a superior sheet for use as a cereal inner wrap.
The invention having now been disclosed and described in detail, it is apparent that various modifications thereof are possible without departing from the spirit thereof. Therefore, no limitations on the invention are intended except as specifically set forth in the appended claims.
We claim:
1. A method for obtaining a substantially dimensionally stable, waxed polyethylene sheet which comprises:
a. passing a polyethylene film having a thickness of between 0.0005 and 0.005 inches into contact with a molten petroleum wax composition maintained at a temperature sufficiently above 130 F. to allow said film to reach a temperature of between 130 F. and the softening point of said film,
. metering any excess wax from said film to leave on at least one surface of said film between 1 lb. and 10 lbs. of wax composition evenly distributed on each ream of 3,000 sq. ft. of said film,
. stretching said film in the machine direction while in contact with said molten wax composition by an amount between 5 and 20 percent of the original length of said film, and
d. cooling said waxed and stretched film to solidify said wax composition coating.
2. A method according to claim 1 wherein said contacting, metering, stretching and cooling steps are carried out at a speed between 200 and 500 feet per minute and said stretching is carried out to the extent of between and 18 percent of the original film length.
3. A method according to claim 2 wherein the weight of said wax composition after said metering step is between 3 and 6 lbs. per ream.
4. A method according to claim 3 wherein said polyethylene film is between 0.001 in. and 0.0025 in. in thickness.
5. A method according to claim 4 wherein said polyethylene film has a surface which is treated to be receptive to fluid coatings.
6. A method for obtaining a dimensionally stable wax-coated polyethylene web suitable for use in highspeed packaging operations which comprises applying a molten petroleum wax composition to at least one surface of a polyethylene web having a thickness of between 0.0005 in. and 0.005 in., maintaining said wax coating in a molten state and said polyethylene web at a temperature between about 130 F. and the softening temperature of the polyethylene while mechanically stretching said coated polyethylene web in a machine direction by an amount between about 5 percent and 20 percent, and subsequently chilling said coated and stretched web to complete solidification of said wax composition coating.
7. A method according to claim 6 wherein said wax composition is applied to a surface treated polyethylene web traveling at between about 200 and 500 feet per minute, said coated polyethylene web being stretched by an amount between 12 percent and 15 percent.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3.751.281 Dat d August 7, 1973 Inventor(s) James Thomas Peterson and Mitsuzo Shida It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Z In. Column 5-, in Table II between line 1%.; which reads P.M.P.) and line 17, which starts "The data in the above table insert the following tabular data:
I r MVTR in i Gm/M /ZH Hours Uncoated Polyethylene Film 6.0
Waxed, Unst r'etched Polyethylene Film -0 .-62.l. 0
Waxed Polyethylene Film, Stretched 0,50 ,5' 12% During Waxing In Column 5 in Table III in the fourth column of the table, delete one instance of the word *Caliper from the column heading and add mil after each of the data in the column.
Signed and sealed this 27th day of, August 1974 (SEAL) Attest:
MCCOY GIBSQN, JR. C. MARSHALL DANN Y Attestlng Officer y Commissioner of Patents US COMM-DC 00376-1 69 FORM PO-1050 (10-69) v a us sovzmmirn mumps OFFICE 1 nos o-3 ss'au,

Claims (6)

  1. 2. A method according to claim 1 wherein said contacting, metering, stretching and cooling steps are carried out at a speed between 200 and 500 feet per minute and said stretching is carried out to the extent of between 10 and 18 percent of the original film length.
  2. 3. A method according to claim 2 wherein the weight of said wax composition after said metering step is between 3 and 6 lbs. per ream.
  3. 4. A method according to claim 3 wherein said polyethylene film is between 0.001 in. and 0.0025 in. in thickness.
  4. 5. A method according to claim 4 wherein said polyethylene film has a surface which is treated to be receptive to fluid coatings.
  5. 6. A method for obtaining a dimensionally stable wax-coated polyethylene web suitable for use in high-speed packaging operations which comprises applying a molten petroleum wax composition to at least one surface of a polyethylene web having a thickness of between 0.0005 in. and 0.005 in., maintaining said wax coating in a molten state and said polyethylene web at a temperature between about 130* F. and the softening temperature of the polyethylene while mechanically stretching said coated polyethylene web in a machine direction by an amount between about 5 percent and 20 percent, and subsequently chilling said coated and stretched web to complete solidification of said wax composition coating.
  6. 7. A method according to claim 6 wherein said wax composition is applied to a surface treated polyethylene web traveling at between about 200 and 500 feet per minute, said coated polyethylene web being stretched by an amount between 12 percent and 15 percent.
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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4086317A (en) * 1974-04-08 1978-04-25 Oji Yuka Goseishi Kabushiki Kaisha Process for production of a synthetic paper improved against dusting trouble
US4172910A (en) * 1978-03-28 1979-10-30 Asten Group, Inc. Coating of papermaking fabrics
US4238533A (en) * 1976-04-16 1980-12-09 La Cellophane Coating process and apparatus
US4275097A (en) * 1978-03-29 1981-06-23 Coors Container Company Protective coating for cans and methods for application of coating thereto
US4897235A (en) * 1985-12-21 1990-01-30 Wolff Walsrode Aktiengesellschaft Process for imparting a surface coating to films
US5155160A (en) * 1988-05-02 1992-10-13 James River Ii, Inc. Polyolefin films having improved barrier properties
US5709747A (en) * 1994-04-25 1998-01-20 Avgol Nonwoven Industries Coating selective zones of thin webs to change the pervious character thereof, using a cover
US20050120842A1 (en) * 2003-12-05 2005-06-09 Fuji Photo Film Co., Ltd. Cutting method of fabric material
US20050137342A1 (en) * 2003-12-19 2005-06-23 Krishnaswamy Rajendra K. Polyethylene blend films
US20060244185A1 (en) * 2005-04-29 2006-11-02 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
US20060244184A1 (en) * 2005-04-29 2006-11-02 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
US20090273115A1 (en) * 2006-03-30 2009-11-05 Makoto Morikawa Method of producing film

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2321635A (en) * 1940-11-26 1943-06-15 Du Pont Treatment of polyamide films
US2627088A (en) * 1950-03-22 1953-02-03 Du Pont Preparation of oriented coated films
US2880057A (en) * 1958-01-22 1959-03-31 Du Pont Treatment of filaments to improve strength in tension
US3068516A (en) * 1960-06-01 1962-12-18 Union Carbide Corp Extruded contour coating
US3140957A (en) * 1960-02-23 1964-07-14 Kurashiki Rayon Co Heat treatment of fibers
US3504075A (en) * 1967-10-26 1970-03-31 Eastman Kodak Co Method of manufacturing high-gloss polymeric films
US3506751A (en) * 1968-05-03 1970-04-14 Continental Can Co Method of drawing plastic containers
US3565985A (en) * 1969-04-10 1971-02-23 Dow Chemical Co Method of preparing multilayer plastic articles

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2321635A (en) * 1940-11-26 1943-06-15 Du Pont Treatment of polyamide films
US2627088A (en) * 1950-03-22 1953-02-03 Du Pont Preparation of oriented coated films
US2880057A (en) * 1958-01-22 1959-03-31 Du Pont Treatment of filaments to improve strength in tension
US3140957A (en) * 1960-02-23 1964-07-14 Kurashiki Rayon Co Heat treatment of fibers
US3068516A (en) * 1960-06-01 1962-12-18 Union Carbide Corp Extruded contour coating
US3504075A (en) * 1967-10-26 1970-03-31 Eastman Kodak Co Method of manufacturing high-gloss polymeric films
US3506751A (en) * 1968-05-03 1970-04-14 Continental Can Co Method of drawing plastic containers
US3565985A (en) * 1969-04-10 1971-02-23 Dow Chemical Co Method of preparing multilayer plastic articles

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4086317A (en) * 1974-04-08 1978-04-25 Oji Yuka Goseishi Kabushiki Kaisha Process for production of a synthetic paper improved against dusting trouble
US4238533A (en) * 1976-04-16 1980-12-09 La Cellophane Coating process and apparatus
US4172910A (en) * 1978-03-28 1979-10-30 Asten Group, Inc. Coating of papermaking fabrics
US4275097A (en) * 1978-03-29 1981-06-23 Coors Container Company Protective coating for cans and methods for application of coating thereto
US4897235A (en) * 1985-12-21 1990-01-30 Wolff Walsrode Aktiengesellschaft Process for imparting a surface coating to films
US5155160A (en) * 1988-05-02 1992-10-13 James River Ii, Inc. Polyolefin films having improved barrier properties
US5709747A (en) * 1994-04-25 1998-01-20 Avgol Nonwoven Industries Coating selective zones of thin webs to change the pervious character thereof, using a cover
US20050120842A1 (en) * 2003-12-05 2005-06-09 Fuji Photo Film Co., Ltd. Cutting method of fabric material
US7536937B2 (en) * 2003-12-05 2009-05-26 Fujifilm Corporation Cutting method of fabric material
US20050137342A1 (en) * 2003-12-19 2005-06-23 Krishnaswamy Rajendra K. Polyethylene blend films
WO2006118906A2 (en) * 2005-04-29 2006-11-09 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
EP2251372A1 (en) * 2005-04-29 2010-11-17 The Procter and Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
US20060244184A1 (en) * 2005-04-29 2006-11-02 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
WO2006118909A3 (en) * 2005-04-29 2007-02-08 Procter & Gamble Polymeric film exhibiting improved anti-blocking characteristics and process of making
WO2006118906A3 (en) * 2005-04-29 2007-03-01 Procter & Gamble Polymeric film exhibiting improved anti-blocking characteristics and process of making
US20060244185A1 (en) * 2005-04-29 2006-11-02 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
US9637603B2 (en) * 2005-04-29 2017-05-02 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
WO2006118909A2 (en) * 2005-04-29 2006-11-09 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
US8158849B2 (en) 2005-04-29 2012-04-17 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
CN101166780B (en) * 2005-04-29 2012-06-20 宝洁公司 Polymeric film exhibiting anti-blocking characteristics and process of making
CN101166491B (en) * 2005-04-29 2012-07-04 宝洁公司 Polymeric film exhibiting improved anti-blocking characteristics and process of making
US8304599B2 (en) 2005-04-29 2012-11-06 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
US20130030399A1 (en) * 2005-04-29 2013-01-31 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
US9096731B2 (en) * 2005-04-29 2015-08-04 The Procter & Gamble Company Polymeric film exhibiting improved anti-blocking characteristics and process of making
US20150314490A1 (en) * 2005-04-29 2015-11-05 The Procter & Gamble Company Polymeric Film Exhibiting Improved Anti-Blocking Characteristics and Process of Making
US20090273115A1 (en) * 2006-03-30 2009-11-05 Makoto Morikawa Method of producing film

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