EP0644911A1 - Fluorine treatment of polyolefin films - Google Patents
Fluorine treatment of polyolefin filmsInfo
- Publication number
- EP0644911A1 EP0644911A1 EP93914343A EP93914343A EP0644911A1 EP 0644911 A1 EP0644911 A1 EP 0644911A1 EP 93914343 A EP93914343 A EP 93914343A EP 93914343 A EP93914343 A EP 93914343A EP 0644911 A1 EP0644911 A1 EP 0644911A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- film
- cling
- flourinated
- partially
- films
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
- B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
- C08J7/126—Halogenation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2264/00—Composition or properties of particles which form a particulate layer or are present as additives
- B32B2264/10—Inorganic particles
- B32B2264/102—Oxide or hydroxide
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2305/00—Condition, form or state of the layers or laminate
- B32B2305/70—Scrap or recycled material
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/728—Hydrophilic
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/75—Printability
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2439/00—Containers; Receptacles
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised 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
Definitions
- the present invention relates generally to thermoplastic films and, more particularly, to partially fluorinated thermoplastic films especially well suited for use in various applications.
- One type of polyolefin film, stretch/cling films, is useful in a wide variety of fields including the bundling and packaging of food and other goods.
- One application of particular relevance to the present invention is in the bundling of goods for shipping and storage such as the bundling of large rolls of carpet, fabric or the like for shipping.
- An important subset of these bundling applications is in the containment and unitizing of pallet loads.
- the tension in the stretched film may also cause the film to be more susceptible to punctures and tears.
- polyolefin films, as a whole to have good stretch, tensile, puncture resistance and tear resistance properties. Thermal stability of the various film components is important for the recycling of edge trim and film scrap generated in the various film production processes.
- tackifying additives include polybutenes, terpene resins, alkali metal stearates and hydrogenated rosins and rosin esters.
- tackifying additives may not be desirable. These additives have a tendency to accumulate on the stretch wrapping apparatus often requiring additional periodic cleaning and maintenance. They also can migrate into the bundled or unitized articles resulting in damage to such articles, as well as migrating throughout a film, even a multilayer film, causing tackiness on both sides. In palletizing operations, this may cause the film on adjacent pallets to cling together resulting in tear, puncture or other damage to the wrap and jeopardizing the integrity of the unitized load.
- slip is defined in terms of coefficient of friction. In other words, it is desirable that the "outer" side of the film have a low coefficient of friction in contact with another object, particularly another like film.
- slip can be imparted to the film or improved through the use of various well-known slip, anti-cling and/or antiblock additives including silicas, silicates, diatomaceous earth and various lubricants.
- film cling properties can be altered by exposure to a corona discharge.
- the reactivity of discharge particles can alter the surface chemistry of the film and consequently its physical characteristics. The effect of such exposure can be observed by changes in film surface energy.
- multilayer films has gained popularity. With a multilayer film, one can obtain a stretch/cling wrap having cling properties on one side and slip properties on the other side. (See for example, U.S. Patent 4,518,654).
- U. S. Patent 3,647,613 to Scotland discloses a surface fluorinated high density polyethylene used for making containers suitable for storing hydrocarbons.
- the HDPE surface containing a concentration of 0.01 to 30 micrograms of fluorine per square centimeter was said to improve permeability characteristics to gasoline.
- U. S. Patent 4,880,675 discloses plastic containers comprising a polyethylene inner layer coextruded with a polypropylene outer layer wherein the inner layer is treated with a reactive fluorine source. Such treatment is said prevent the absorption of flavor or aroma compounds by the container lining.
- U. S. Patents 4,264,750 and 4,404,256 to Anand et al. disclose a process for making fluorinated low energy polymer surfaces by exposure to ions or radicals of fluorinated species in a cold plasma and polymers having a substantially completely fluorinated surface of low surface energy which is substantially oxygen free.
- Pretreatment of Polymer webs by Means of Fluorine and Milker and Koch, "Fluorine Makes Plastics Flexible”; describe a fluorination process for producing polymer films said to have good adhesion properties. The process is said to alter the surface on a more or less permanent basis so that the polar character of the material is increased.
- the present invention resides in part in the discovery that the properties of a polyolefin film are surprisingly enhanced following partial fluorination of one or both exterior surfaces of the film.
- the treatment comprises exposing one or both surfaces of the film to a dilute mixture of a fluorination species in a carrier gas for a time period less than that required to achieve complete surface fluorination and subsequently exposing the partially fluorinated film surface to oxygen.
- the present invention provides a thermoplastic film having excellent cling properties, even without the use of a tackifying additive.
- This invention further provides films with enhanced wettability, printability and/or inkability.
- the present invention further provides a multilayer stretch/cling film having excellent cling properties on one side and excellent slip properties on an opposite side, even in a highly stretched state.
- the present invention provides a multilayer stretch/cling film which, as a whole, possesses desirable stretch, tensile strength, puncture resistance, tear resistance and thermal stability properties.
- the present invention provides a process for producing such polyolefin films.
- One or both surfaces of the coextruded layers of a film are partially fluorinated to enhance properties.
- the fluorination reaction catalyzes an oxygenation by- reaction upon exposure to air.
- the surface to be treated is exposed to a suitable source of reactive fluorine, such as, for example, fluorine-containing plasmas, fluorine-containing gas mixtures, fluorine dissolved in solvents, UV activated fluorine gas mixtures, and the like.
- a suitable source of reactive fluorine such as, for example, fluorine-containing plasmas, fluorine-containing gas mixtures, fluorine dissolved in solvents, UV activated fluorine gas mixtures, and the like.
- a suitable source of reactive fluorine such as, for example, fluorine-containing plasmas, fluorine-containing gas mixtures, fluorine dissolved in solvents, UV activated fluorine gas mixtures, and the like.
- any of the equipment and methodology for fluorination described in Volkman or Milker and Koch can be
- Processes for fluorinating one or both sides of film material in either batch or continuous operations are known.
- the film is introduced into a reaction chamber generally having special locks at either end so that the film may be continuously passed through the chamber without permitting gas to escape.
- the locks typically have a low pressure seal provided by a vacuum pump.
- Fluorine is metered from compressed cylinders generally pressurized with the diluent gas to achieve higher fill pressure. Gas exiting the reaction chamber is compressed, combined with makeup gas and recycled to maintain a steady gas flowrate through the reactor.
- An absorber may be used to remove HF byproduct gas from the recycle stream. Very pure nitrogen is provided as flush and diluent gas. Waste fluorine can be catalyzed to hydrogen fluoride then absorbed by an absorbent such as calcium hydroxide.
- the duration of the exposure to F 2 and air required to obtain the desired enhancement of properties such as cling, slip, printability, ink retention and wetabili * ⁇ y depends on the conditions of exposure, the film cosmosition and properties, F 2 concentration, etc. It is important that the fluorination reaction is not permitted to go to completion, i.e. to replace a majority of the available hydrogen atoms attached to the carbon backbone. Fluorination is substantially complete if a majority of the available surface hydrogen atoms are substituted for fluorine atoms so that there is relatively little further fluorination upon further continued fluorine exposure. Partial fluorination is indicated by a dispersive surface energy less than the corresponding polar surface energy, in contrast to a surface energy higher than the polar surface energy when complete surface fluorination is achieved.
- F 2 exposure times of from 1 to 30 minutes are suitable.
- Subsequent oxygenation of the film surface is generally instantaneous upon exposure to air, although exposure to oxygen can be extended to ensure complete oxygenation without adversely affecting the desirable film properties.
- the amount of F 2 needed to enhance properties is relatively minor. Cling and block are improved in some instances with a fluorine:carbon surface stoichiometry, as low as 0.001, as determined by X-ray photoelectron spectroscopy (XPS) . However, if the fluorine:carbon surface stoichiometry is too high, the surface may not become activated for reaction to oxygen, a low polarity surface is produced and cling is adversely affected.
- the fluorine:carbon surface stoichiometry is preferably in the range of from about 0.001 to about 3.0, more preferably about 0.01 to about 1.0, more preferably from about 0.01 to about 0.15. The amount of oxygen bonds formed by the activated surface depends on surface F/C stoichiometry and the substrate material.
- a suitable 0/C stoichiometry is about 10 % or greater.
- the extent of surface activation for any given substrate material is believed to undergo a maximum at a specific degree of surface fluorination (i. e. F/C ratio) .
- fluorination is thought to proceed by a radical mechanism by the abstraction of hydrogens.
- Oxygenation increases the polar surface energy which is a measure of hydrophilicity.
- the radicals can also react with carbons on neighboring chains producing a degree of surface crosslinking. Crosslinking reduces any tendency for interfacial diffusion (i. e. blocking) .
- Thermoplastic films produced in accordance with the present invention have excellent cling properties on the cling layer and slip properties on the non-cling layer.
- the use of tackifying additives can be avoided because of the excellent cling properties of the cling layer polymer against a partially fluorinated non-cling surface.
- the treatment while enhancing the cling property of the stretch/cling film does not, however, substantially increase the tendency to block, and generally a substantial decrease in the block is found.
- the non cling layer is preferably treated, however either side may be treated.
- the present thermoplastic films, as a whole, additionally have desirable stretch, tensile, puncture resistance and tear resistance properties.
- thermoplastic films of the present invention have excellent thermal stability, and edge trim scrap can be processed without significant loss of film performance.
- the thermoplastic film preferrably comprises a cling layer and a non-cling layer, wherein one or both of the exterior surfaces is partially fluorinated.
- the cling layer comprises a polymer of two or more monomers, wherein a first monomer comprises ethylene and a second monomer comprises an acrylate.
- Acrylate in the singular, refers to both a single acrylate and combinations of different acrylates. These polymers will generally be referred to as ethylene-acrylate (or EA) polymers.
- R is selected from hydrogen or a hydrocarbon group having from 1 to 22 carbon atoms, preferably an alkyl, aryl, aromatic, olefin or the like hydrocarbon group and wherein R' is selected from the same or different of these hydrocarbon groups.
- Preferred acrylates comprise those wherein R is selected from hydrogen or an alkyl group and wherein R' is the same or different of such alkyl group.
- Specific examples of preferred acrylates include methyl acrylate, ethyl acrylate, propyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate, decyl acrylate, octadecyl acrylate, methyl ethacrylate, ethyl methacrylate, n-butyl methacrylate and the like. Of these, methyl acrylate is particularly preferred.
- the EA polymer comprises an acrylate content of between about 2% to about 40%, more preferably between about 10% to about 35%, most preferably between about 20% to about 30%, and especially between about 24% to about 28% by weight based upon the weight of the EA polymer.
- the EA polymer may have a wide range of melt indexes (MI) , generally between about 0.1 to about 30 dg/min, more preferably between about 1 to about 10 dg/min (ASTM D- 1238, Condition E) .
- the EA polymer may also comprise one or more free radically polymerizable termonomers. Suitable examples include, but are not limited to, vinyl esters, acrylic acids (i.e. methacrylic and ethacrylic acid) , other acrylates, carbon monoxide and the like. These additional termonomers will generally be present in small amounts, usually less than a total of about 10% by weight based upon the weight of the EA polymer.
- tackifying additive may be added to the EA polymer during the polymerization reaction or subsequently blended in to improve the cling properties of the film.
- tackifying additives are well known in the art including, for example, polybutenes, atactic polypropylenes, terpene resins, hydrogenated rosins, rosin esters and other like hydrocarbon tackifying resins. It should be noted, however, that the aforedescribed EA polymers produce films of sufficient cling so as to not require the use of a tackifying additive.
- the use of tackifying additives is contemplated by this invention but is not necessarily preferred.
- the EA polymer is essentially free of a tackifying additive.
- the cling layer preferably comprises between about 5% to about 95%, more preferably between about 5% to about 35%, most preferably between about 10% to about 20% of the combined thickness of the cling and non- cling layers.
- the second layer of the multilayer stretch film comprises a non-cling layer opposite the cling layer.
- the non-cling layer comprises any suitable polyolefin or combination of polyolefins such as polyethylene, polypropylene, copolymers of ethylene and propylene, and polymers obtained from ethylene and/or propylene copolymerized with minor amounts of other olefins, particularly C4-C12 olefins.
- MDPE medium density polyethylene
- LLDPE linear low density polyethylene
- olefin comonomers include 1-butene, 1-hexene, 1-octene and 4- methyl pentene-1.
- Suitable MDPEs include those having a density in the range of from about 0.92 to about 0.95 g/cc and a wide ranging MI, generally up to about 30 dg/min preferably between about 0.5 to about 10 dg/min.
- Suitable LLDPEs include those having a density greater than about 0.900 g/cc more preferably in the range of from about 0.900 to about 0.940 g/cc.
- the LLDPEs may also have a wide ranging MI, generally up to about 30 dg/min, preferably between about 0.5 to about 10 dg/min.
- Suitable polypropylene is normally solid and isotactic, i.e., greater than 90% hot heptane insolubles, having wide ranging melt flow rates of from about 0.1 to about 300 dg/min. As is known, such polypropylene is normally crystalline with a density range of from about 0.89 to about 0.91 g/cc for isotactic polypropylene.
- Employing polypropylene in the non-cling layer has the additional advantage of imparting abrasion resistance thereto.
- the non-cling layer preferably comprises between about 5% to about 95%, more preferably between about 65% to about 95%, most preferably between about 80% to about 90% of the combined thickness of the cling/non- cling layers.
- Alternate embodiments of the invention provide wettable, printable and/or inkable polyolefin films.
- the single or multilayer films as described above or other polyolefin films such as homo or co- polyethylene, homo or co-polypropylene, ethylene, vinyl acetate and the like may be partially flourinated to enchance wettability, printability and/or ink retention.
- wetting is the idea that maximum interfacial adhesive bond strength is achieved when the adhesive comes into contact with the adherend and the intermolecular forces across the interface are maximized.
- the partially flourinated films of this invention have increased wettability when compared to the non-flourinated films. Wettability is measured using standard treat solutions well known in the art (ASTM D2578-94) . ASTM D2578-94 is hereby incorporated by reference. Wettabiltiy is also commonly reported in terms of polar surface energy which is measured by the geometric mean equation as shown for example on page 103 of Polymer Interface and Adhesion. Dekker Pub. 1982.
- the partially flourinated film becomes more receptive to inks, dyes, pigments, adhesives, tackifiers, hot melt adhesives and the like yielding stronger bonds.
- the wettability of the partially flourinated film is substantially improved when compared to the non flourinated films.
- the partially flourinated films will have a polar surface energy of at least about 10 dynes/cm, preferrably at least about 15 dynes/cm, even more preferrably at least about 20 dynes/cm, even more preferrably at least about 30 dynes/cm.
- this invention contemplates partially flourinated films with adhesive compositions coated thereon for use in many applications such as tapes and labels.
- Suitable adhesives include hot melt compositions, pressure sensitive adhesive composistions, contact adhesive compositions and the like. Examples include EVA based hot melts, polyurethanes and polyacrylates.
- This invention also contemplates films partially flourinated without adhesives used in a variety of applications such as packages, bags, containers and the like.
- the partially flourinated films are also more receptive to inks, dyes and other printing or coloring agents known to those of ordinary skill in the art including Fuchsine (Cl 42510) , Calcocid Greens (Cl 44090) , titanium dioxide, colloidal carbon, graphite, ceramics, clays, phosphor particles, metal particles and the like.
- the various films may also include one or more intermediate layers between the layers for any one of a number of well-known purposes such as, for example, to provide structural support, to modify the overall physical properties balance of the film, to utilize the recycle trim and scrap or to provide a barrier layer to oxygen or other gases.
- this intermediate layer may comprise the recycle trim and scrap, or may comprise any other suitable polymer.
- the intermediate layer( ⁇ ) is optional and should not be considered a limitation on the present invention.
- the film layers of the present invention may, if desired, also include one or more other well-known additives such as antioxidants, ultraviolet absorbers, antistatic agents, release agents, pigments, colorants or the like.
- trim and scrap from the film production process or from suitably recovered and reprocessed films can be recycled into layers, preferably the core structural layer of a three-layer film.
- the EA polymers prefered for use in stretch cling films may be produced by any one of a number of well-known processes such as, for example, those described in U. S. Patent No. 3,350,372, which is incorporated by reference for all purposes as if fully set forth.
- ethylene and any comonomers such as an acrylate to make an EA copolymer and, if desired, another monomer(s) are etered into, for example, a high pressure autoclave reactor along with any one of a number of well-known free radical polymerization initiators (catalysts) suitable for producing EA polymers.
- catalysts include organic peroxides such as, for example, lauroyl peroxide, di-tert butyl peroxide, tert butyl peroxide and various azo compounds.
- the catalyst will be dissolved in a suitable organic liquid such as benzene, mineral oil or the like.
- a suitable organic liquid such as benzene, mineral oil or the like.
- the catalyst is used at a level of between about 50 to about 20,000 ppm, more preferably between about 100 to about 250 ppm based upon the weight of the monomers.
- MDPE, LLDPE and polypropylene may be made by well known Ziegler catalyst processes including gas phase, slurry, solution, and the like and are readily available commercially.
- thermoplastic films of the present invention any one of a number of well-known extrusion or coextrusion (in the case of multilayer films) techniques as disclosed in the previously incorporated references may be utilized.
- extrusion or coextrusion in the case of multilayer films
- any of the blown or chill roll cast processes as disclosed and described in those references is suitable for use in producing thermoplastic films in accordance with the present invention.
- thermoplastic films of the present invention have properties making them especially well suited for use as stretch/cling films, however this use should not be considered a limitation on the present invention.
- these films can be made into other forms, such as a tape, by any one of a number of well-known cutting, slitting and/or rewinding operations.
- Physical properties including, but not limited to, tensile strength, tear strength and elongation can be adjusted over wide ranges by altering the resin types and specifications as appropriate to meet the requirements to a given wrapping, bundling or taping application.
- the thermoplastic film of the present invention is stretch-wrapped by any one of a number of well-known procedures (such as those disclosed in the aforementioned incorporated references) around an article or a plurality of articles preferably so that the cling layer faces inside (towards the article) and the non-cling layer faces outside (away from the article) .
- Typical of articles suitable for bundling, packaging and unitizing with the present thermoplastic film include, but are not limited to, various foodstuffs (canned or fresh) , rolls of carpet, liquid containers and various like goods normally containerized and/or palletized for shipping, storage and/or display.
- I/O cling is reported as the force in grams required to partially peel apart two strips of film.
- a first film strip is attached to a 30 degrees inclined plane with the outside (0) surface (non-cling) facing upward.
- a second 1" X 8" strip is placed on top of the first strip with the inside (I) surface (cling) facing downward. Pressure is applied to the second strip to cause the two strips to stick together. If an evaluation of cling under stretched conditions is asired, both film strips are prestretched and allowed to relax before testing.
- the end of the second strip at the base of the inclined plane is attached, by clip and string, to an apparatus which can exert a strain at a constant rate (Instron 1130) .
- the two strips are then pulled apart at a crosshead speed of 10 cm/min until the aforementioned string is parallel with the base of the inclined plane. The force at this point is reported as cling.
- Block is reported as the 180 degree peel strength of the outside surface (non-cling) of a first film specimen pressed with 200 psi at 154 degrees F (1.378 MPa at 103.3 degrees C) against the inside surface (cling) of a second film specimen for a specified length of time.
- the block, cling or slip of multicompositional, multilayer films refers to properties the film has when in physical contact with itself such as on a roll or a wrapped pallet. Such properties are generally referenced by noting the location of the surfaces or layers in contact (i.e. inside/outside (I/O)).
- a MDPE film was made from a resin having a melt index of 2 and a density of 0.92 g/cc produced in a gas phase reactor.
- the film was fluorinated using two different degrees of fluorination. One film had high fluorine concentration at the surface and the other a low fluorine concentration.
- Film surface stoichiometry for 0/C and F/C as determined by x-ray spectroscopy (XPS) is given in Table I.
- Fluorination was conducted by a commercial fluorination service which is believed to have used a conventional batch apparatus wherein the film substrate was exposed to a gas mixture of molecular fluorine in a pure nitrogen carrier gas for a set period of time in a reactor vessel.
- the fluorinated films were handled normally in air prior to physical testing.
- film interfaces were prepared by pressing together a cling layer surface comprising a 24 % EMA film and a non-cling layer surface comprising the fluorinated MDPE described above.
- the pressing conditions were 200 psi pressure and 158 degrees F temperature (1.378 MPa and 105.5 degrees C) for a set period of time.
- the blocking tendency was gauged by the peel force required to separate the films.
- interfaces made with both the low and high fluorinated MDPE required very little peel force compared to the film interface lacking a fluorinated surface. Furthermore, the low fluorinated film interface was almost as resistant to blocking as the high fluorinated film interface.
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- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
Claims
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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US893282 | 1992-06-04 | ||
US07/893,282 US5225257A (en) | 1992-06-04 | 1992-06-04 | Fluorine treatment of stretch/cling films |
US5905793A | 1993-05-07 | 1993-05-07 | |
US59057 | 1993-05-07 | ||
PCT/US1993/005273 WO1993024559A1 (en) | 1992-06-04 | 1993-06-04 | Fluorine treatment of polyolefin films |
Publications (1)
Publication Number | Publication Date |
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EP0644911A1 true EP0644911A1 (en) | 1995-03-29 |
Family
ID=26738308
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP93914343A Ceased EP0644911A1 (en) | 1992-06-04 | 1993-06-04 | Fluorine treatment of polyolefin films |
Country Status (4)
Country | Link |
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EP (1) | EP0644911A1 (en) |
JP (1) | JPH07507582A (en) |
CA (1) | CA2118230A1 (en) |
WO (1) | WO1993024559A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE1008320A3 (en) * | 1994-04-19 | 1996-04-02 | Solvay | Surface treatment method for the articles with at least one plastic. |
BE1008319A3 (en) * | 1994-04-19 | 1996-04-02 | Solvay | Articles based polyolefins printed using pvc inks and methods of making. |
US7316869B2 (en) | 2003-08-26 | 2008-01-08 | Intel Corporation | Mounting a pellicle to a frame |
US7314667B2 (en) | 2004-03-12 | 2008-01-01 | Intel Corporation | Process to optimize properties of polymer pellicles and resist for lithography applications |
DE102008059125A1 (en) * | 2008-11-26 | 2010-05-27 | Air Liquide Deutschland Gmbh | Method and device for functionalizing a target area of a surface |
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Publication number | Priority date | Publication date | Assignee | Title |
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BE811644A (en) * | 1973-03-16 | 1974-06-17 | POLYOLEFINS PRODUCTION PROCESS | |
JPS58168630A (en) * | 1982-03-29 | 1983-10-05 | バツテル・デイベロプメント・コ−ポレ−シヨン | Surface fluorination |
US4508781A (en) * | 1982-06-07 | 1985-04-02 | The United States Of America As Represented By The Secretary Of Agriculture | Fluorination by inorganic fluorides in glow discharge |
JPS6335632A (en) * | 1986-07-30 | 1988-02-16 | Kuraray Co Ltd | Sheet-like fluorinated polymer structure and its production |
US4764405A (en) * | 1987-07-22 | 1988-08-16 | Air Products And Chemicals, Inc. | Method for increasing barrier properties of thermoplastic substrates |
DE4006809A1 (en) * | 1990-03-05 | 1991-09-12 | Alkor Gmbh | Substrate coating process for furniture, etc. - by surface-fluorination of polyolefin film contg. non-fluorine-contg. (in)organic fillers, processing additives, pigments, etc. |
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1993
- 1993-06-04 WO PCT/US1993/005273 patent/WO1993024559A1/en not_active Application Discontinuation
- 1993-06-04 CA CA002118230A patent/CA2118230A1/en not_active Abandoned
- 1993-06-04 EP EP93914343A patent/EP0644911A1/en not_active Ceased
- 1993-06-04 JP JP6500865A patent/JPH07507582A/en active Pending
Non-Patent Citations (1)
Title |
---|
See references of WO9324559A1 * |
Also Published As
Publication number | Publication date |
---|---|
JPH07507582A (en) | 1995-08-24 |
WO1993024559A1 (en) | 1993-12-09 |
CA2118230A1 (en) | 1993-12-09 |
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