Waste packing system and film

Information

  • Patent Grant
  • 10287094
  • Patent Number
    10,287,094
  • Date Filed
    Friday, February 12, 2016
    8 years ago
  • Date Issued
    Tuesday, May 14, 2019
    5 years ago
Abstract
The present invention is directed to a waste packaging system, a method of storing waste and to a film for use in this system and method.
Description

The present invention is directed to a waste packaging system, a method of storing waste and to a film for use in this system and method.


A lot of waste products produce smells that are annoying to the environment. Examples are decayed food, kid nappies and cat litter.


In the prior art there are many films that could be used for protection from malodors. As it is well known in the art, the use of materials like EVOH, PVDC, polyacrylonitrile is recommended in order to not allow malodors escape from the container (eg bag or other configuration) and create an unpleasant atmosphere.


There are also a lot of known configurations of packing a certain length of film (eg 20 meters) in a compressed form (eg in a cassette). Examples of the representative cassettes are shown in U.S. Pat. No. 4,934,529 or U.S. Pat. No. 3,536,192.


Generally the cassette comprises a tubular core, casing wall, cassette bottom and lid. The film is stored in an area between tubular core, casing wall and cassette bottom in a compressed configuration. The flexible tubing is dispensed from the cassette. After the malodorous item is thrown into the bag the core or the lid is rotated and the flexible tube is twisted so that it closes as hermetically as possible the waste/environment area. To dispose the next diaper the user opens the lid and inserts the diaper. The previous pack is pushed downward and a new knot is formed by twisting the tube above the newly deposited diaper. Thus the device stores the diapers in a series of individually wrapped packages in the storage chamber, each package being separated from adjacent packages by twists in the tube.


Separation of one piece of flexible film from the next by means of a rotary knife is preferred.


In the prior art as a general rule the separation of each piece of the film in which the smelly item is contained from the next piece of the film is done with a twisting mechanism. This twist separates in a “hermetic” way the one piece from the other.


That is to say, it is a problem in the prior art techniques that the twist is never really hermetic. Odour molecules being extremely small have the capability to escape through the folds so the odour starts to be noticeable after a few days. There is still a need for a more hermetic way to isolate each individual pack with the next one.


Methods based on heat sealing have been proposed in the prior art as for example in EP 0005660. This concept is quite complicated as it uses sheaths to form discrete packages. The complex nature of this design makes it expensive to manufacture.


According to the prior art document U.S. Pat. No. 4,869,049, the use of electricity is to be avoided anywhere near babies therefore this approach has not been commercially successful. So, twisting is the preferred option for separating one pack from the next.


Heat sealing and cutting as means to separate each pack from the next is also an object of U.S. Pat. No. 6,516,588. In this reference there is no mention to the use of a low voltage battery. So, in general this method is not suitable enough as it involves electricity of high voltage and this is to be avoided for this sensitive application. Also, there is no reference to a low voltage battery.


Further, U.S. Pat. No. 6,516,588 does not refer to a suitable film that can be sealed efficiently and also through pleats and wrinkles (which are unavoidable during this kind of application).


According to this application “the plastic tubing may be any plastic tubing known in the art” as described in col. 4 lines 30-31.


Further, U.S. Pat. No. 4,612,221 refers to a thin film incorporating oxygen barrier material. The film comprises a cling agent (additive which offers cling property) and is suitable to be used as a food wrap. There is no mention of the possibility of the film to be used in a waste packing system. Also the cling additive makes it unsuitable in a waste packing system due to a number of reasons such as difficult unwinding, waxy feeling, more complicated production process etc.


The present invention provides a safe and simple apparatus that is quick and easy to operate, that stores soiled nappies in flexible tubing in a very hygienic way so that they can be disposed collectively after a certain amount of time. It also provides a suitable plastic film to be used accordingly.


SUMMARY OF THE INVENTION

The present invention in one aspect is directed to a device comprising

    • 1. a dispensing apparatus wherein a plastic film with weight/surface ration less than 20 grams per square meter is stored
    • 2. a bin wherein a fusion seal apparatus is located
    • 3. a fusion seal apparatus comprising a battery with a maximum voltage of 20V.


The battery may be rechargeable or non-rechargeable. Preferably, it is rechargeable.


Also another object of the present invention is a method of packing waste items by

    • 1. pulling out plastic film of weight/surface ration less than 20 grams per square meter from a dispensing apparatus
    • 2. putting a waste item in a suitable length of the film
    • 3. closing hermetically the plastic film with the use of a fusion seal where the seal is between a part of the film and another part of the same or other film, where the sealed parts are put sequentially in a bin.


The fusion seal is preferably done with a fusion seal apparatus comprising a battery with a maximum voltage of 20V.


Also another object of the present invention is a plastic film comprising at least a layer comprising at least 50% per weight of polyethylene homopolymer and/or copolymer, where the weight/surface ratio is less than 20 grams per square meter and the film can be heat sealed with the thermal energy transferred with a battery with a voltage of less than 20 V.


In a preferred embodiment, the present invention provides a multilayer plastic film comprising at least

    • 1. an outer layer comprising of polyethylene homopolymer and/or copolymer
    • 2. an internal layer comprising at least one oxygen barrier material
    • 3. an inner layer comprising polyethylene homopolymer and/or copolymer,


      where the weight/surface ratio is less than 20 grams per square meter and the film can be heat sealed with the thermal energy transferred with a battery with a voltage of less than 20 V.


In a preferred embodiment, the outer and/or inner layer comprise at least 50% per weight of polyethylene homopolymer and/or copolymer.


The film preferably does not contain any cling agents.


Definitions

In this application the following definitions are used:


The term “waste” refers to any receptable that is useless and has to be disposed of properly. For example, the term waste includes diapers or other dirt.


The term “dispensing apparatus” refers to any apparatus where the film is stored before the application process. Examples are cassettes or reels.


The term “cassette” refers to any container wherein the film can be put. Often the film is in compressed form. The cassette is usually plastic and circular but other configurations may be possible.


The term “fusion seal” refers to the sealing of film by melting. A different kind of seal is by twisting the plastic film or by used an adhesive (in this latter case a kind of seal is made by pressure alone).


The term “bin” refers to a container where many waste packs are put one after the other. Each pack comprises a portion of the sealed film and of course the waste inside.


The term “film” refers to a flat or tubular flexible structure of thermoplastic material.


The term “voltage” between two points refers to the electrical driving force that could determine an electric current between these points.


The term “battery” refers to one or more electrochemical cells that convert stored chemical energy to electrical energy.


The term “rechargeable” refers to batteries that are designed in a way to be recharged and used multiple times.


The term “heat shrinkable” refers to a film that shrinks at least 10% in at least one of the longitudinal and transverse directions when heated at 90° C. for 4 seconds. The shrinkability is measured in water according to ASTM 2732. For temperatures like 100° C. or more, glycerine is used as a reference liquid.


The term “total heat shrinkability” refers to the sum of heat shrinkability at the MD direction and heat shrinkability at the TD direction. In all cases, ASTM 2732 is used for measurement of shrinkabilities.


The term “multilayer” refers to a film comprising 2 or more layers.


The phrase “longitudinal direction” or “machine direction” herein abbreviated “MD” refers to a direction along the length of the film.


The phrase “outer layer” refers to the film layer which comes in immediate contact with the outside environment (atmosphere).


The phrase “internal layer” as used herein refers to a film layer located between the outer and the inner layer of the multilayer film. It is not in contact with the atmosphere or the good to be packaged and usually comprises an oxygen barrier material.


The phrase “inner layer” refers to the film layer that comes in direct contact with the product packed. This is also called “sealing layer” as this layer must be hermetically sealed in order to protect the product from ingress of air.


The phrase “abuse layer” refers to a film layer whose main contribution to the film structure is to increase the abuse resistance property. The layer comprises materials which offer high impact strength to the film. Often, the abuse layer is an inner layer of the film, but it can form the outer layer as well. In some embodiments, it may form an internal layer as well.


The phrase “intermediate layer” refers to a film layer whose main contribution to the film structure is to increase the bonding between an oxygen barrier layer and another layer (eg abuse layer, inner layer, outer layer etc).


As used herein, the term “homopolymer” refers to a polymer resulting from polymerization of a single monomer.


As used herein, the term “copolymer” refers to a polymer resulting from polymerization of at least two different polymers.


As used herein, the term “polymer” includes both above types.


As used herein, the term “polyolefin” refers to any polymerized olefin, which can be linear, branched, cyclic, aliphatic, substituted or unsubstituted. More specifically, included in the term polyolefin are homopolymers of olefin, copolymers of olefin, copolymers of an olefin and a non olefinic comonomer (such as ester) etc.


Specific examples include polyethylene homopolymer, polypropylene homopolymer, polybutene homopolymer, ethylene alpha olefin copolymer, propylene alpha olefin copolymer, butene alpha olefin copolymer, ionomer, ethylene ester copolymer etc.


As used herein the term “polyethylene” identifies polymers consisting essentially of the ethylene repeating unit. The ones that have a density more than 0.940 are called high density polyethylene (HDPE), the ones that are have less than 0.940 are low density polyethylene (LDPE).


As used herein the phrase “ethylene alpha olefin copolymer” refers to polymers like linear low density polyethylene (LLDPE), medium density polyethylene (MDPE), very low density polyethylene (VLDPE), ultra low density polyethylene (ULDPE), metallocene catalysed polymers and polyethylene plastomers and elastomers.


As used herein the term “homogeneous ethylene alpha olefin copolymers” refer to ethylene alpha olefin copolymers having a molecular weight distribution less than 2.7 as measured by GPC. Typical examples of these polymers are AFFINITY from DOW or Exact from Exxon.


As used herein the phrase “styrene polymers” refers to styrene homopolymer such as polystyrene and to styrene copolymers such as styrene-butadiene copolymers, styrene-butadiene-styrene copolymers, styrene-isoprene-styrene copolymers, styrene-ethylene-butadiene-styrene copolymers, ethylene-styrene copolymers and the like.


As used herein the phrase “ethylene methacrylate copolymers” refers to copolymers of ethylene and methacrylate monomer. The monomer content is less than 40%.


As used herein the phrase “ethylene vinyl acetate copolymer” or EVA refer to copolymers of ethylene and vinyl acetate.


As used herein the phrase “ethylene ester copolymer” includes any polymer made from ethylene and ester monomers. It is obvious that this term includes EVAs, EMAs and other polymers.


As used herein the term “oxygen barrier polymer” refers to polymers which have the property to limit the passage of oxygen through a film or a layer comprising the polymer. Common materials, are EVOH, PVDC or polyamide. Those polymers usually are comprised in at least one internal layer of the multilayer film.


As used herein, the term EVOH refers to saponified products of ethylene vinyl ester copolymers. The ethylene content is typically in the range of 25 to 50% per mol. All the later references to EVOH ethylene content will be in % per mol.


As used herein the term PVDC refers to a vinylidene chloride copolymer wherein a major amount of the copolymer comprises vinylidene chloride and a minor amount of the copolymer comprises one or more monomers such as vinyl chloride and/or alkyl acrylates and methacrylates.


As used herein the term “polyamide” refers to homopolymers and copolymers. Polyamide 6, polyamide 66, polyamide 12, polyamide 6/66, polyamide 6/12, polyamide elastomers, MXD polyamides and other copolymers are specifically useful for the invention.


As used herein the term “polyester” refers to polymers comprising terephthalate units. Examples of polyesters are PET (polyethylene terephthalate), PBT (polybutylene terephthalate), polyester elastomer (block copolymer comprising ester or ether units), PTT and other similar polymers.


As used herein, the term “ionomer” comprises the copolymers of ethylene and methacrylic or acrylic acid being metal neutralized. An example of such material is Surlyn from Dupont.


As used herein, the term “polypropylene” refers to polymers incorporating propylene structural units. Examples of these, are homo polypropylenes, random copolymers of propylene and ethylene, block copolymers of propylene and ethylene, copolymers or blends of propylene and rubber (such as blends of polypropylene and ethylene propylene rubber), propylene ethylene alpha olefin terpolymers and others.


These polymers may be isotactic, syndiotactic or atactic. Isotactic is preferred.


In line with the above definition, it is noted that for the purposes of the present invention, the term “inner layer” is to be regarded as an additional outer layer of the multilayer film, which is in direct contact with the item to be packaged (i.e. an outer layer of the film which is located on the inside after a packaging process, not exposed to the environment).


As used herein the term “substantially non resilient material” refers to materials or material compounds comprising at least 40% per weight inorganics like calcium carbonate, titanium dioxide, wollastonite, mica, glass fibers, dolomite and the like. The rest percentage per weight can be polyethylene, polypropylene, styrene polymer or other thermoplastic material.


All measurement methods mentioned herein are readily available for the skilled person. For example, they can be obtained from the American National Standards Institute at: www.webstore.ansi.org


All percentages are based on weight per weight ratio, except when otherwise stated.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a perspective view of an embodiment of a presently disclosed apparatus.



FIG. 2 is a perspective view of an embodiment of a presently disclosed apparatus.



FIG. 3 is a side view of an embodiment of a presently disclosed apparatus.





DETAILED DESCRIPTION OF THE INVENTION

The present invention is directed to a device comprising

    • 1. a dispensing apparatus where a plastic film of weight/surface ration less than 20 grams per square meter is stored
    • 2. a bin where a fusion seal apparatus is located
    • 3. a fusion seal apparatus comprising a battery with a maximum voltage of 20V.


The battery preferably is rechargeable.


In some embodiments, the dispensing apparatus has the form of a cassette.


In some embodiments, the voltage is less than 16 V. In some embodiments, the voltage is less than 12 V.


In some embodiments, the temperature for a heat seal is set to less than 100° C., less than 90° C., or less than 80° C. In some embodiments, the sealing time is set to less than 5 seconds, less than 3 seconds, or less than 1 second.


Another aspect of the present invention is a method of packing waste items by

    • 1. pulling out plastic film of weight/surface ration less than 20 grams per square meter from a dispensing apparatus
    • 2. putting a waste item in a suitable length of the film
    • 3. closing hermetically the plastic film with the use of a fusion seal where the seal is between a part of the film and another part of the same or other film, where the sealed parts are put sequentially in a bin.


The fusion seal is preferably done with a fusion seal apparatus comprising a battery with a maximum voltage of 20V.


A still further aspect of the present invention is a method of packing waste items by

    • 1. pulling out plastic film of weight/surface ration less than 20 grams per square meter from a dispensing apparatus
    • 2. putting a waste item in a suitable length of the film
    • 3. closing hermetically the plastic film with the use of a fusion seal where the seal is between a part of the film and another part of the same or other film where the film is able to be sealed through pleats and wrinkles,
      • where the sealed parts are put sequentially in a bin.


A preferred embodiment of the present invention is a method of packing waste items by

    • 1. pulling out plastic film of weight/surface ration less than 15 grams per square meter from a dispensing apparatus
    • 2. putting a waste item in a suitable length of the film
    • 3. closing hermetically the plastic film with the use of a fusion seal where the seal is between a part of the film and another part of the same or other film where the film is able to be sealed through pleats and wrinkles,


      where the sealed parts are put sequentially in a bin.


Also another object of the present invention is a plastic film comprising at least a layer comprising at least 50% per weight of polyethylene homopolymer or copolymer, where the weight/surface ratio is less than 20 grams per square meter and the film can be heat sealed with the thermal energy transferred with a battery with a voltage of less than 20 V.


Also another object of the present invention is a multilayer plastic film comprising at least

    • 1. an outer layer comprising polyethylene homopolymer and/or copolymer
    • 2. an internal layer comprising at least one oxygen barrier material
    • 3. an inner layer comprising polyethylene homopolymer and/or copolymer,


      where the weight/surface ratio is less than 20 grams per square meter and the film can be heat sealed with the thermal energy transferred with a battery with a voltage of less than 20 V.


In a preferred embodiment, one or both of the outer and inner layers comprise at least 50% per weight of polyethylene homopolymer and/or copolymer.


Dispensing Apparatus


A dispensing apparatus of the present invention preferably has the form of a cassette. Nevertheless, other dispensing apparatus are also possible in which a cassette is not used. For example the film can be wound in the form of a mini roll around a paper core. Alternatively, two such mini rolls may comprise the film in such a way that the film wound in the first mini roll will heat seal to the film that is wound in the second mini roll.


Cassette


In a preferred embodiment the cassette useful for the invention is circular in shape (see FIG. 1). Preferably it is made by plastic, eg polypropylene.


It is also possible to be manufactured from other means more friendly to the environment such as paper, biodegradable plastic or non biodegradable plastic where a percentage of “degrading” additives have been added.


Generally, the cassette comprises a tubular core (see reference number 14 in FIG. 1), casing wall (see reference number 12 in FIG. 1), cassette bottom and lid (see reference number 13 in FIG. 1). The film is stored in an area between tubular core, casing wall and cassette bottom in a compressed configuration. The flexible tubing is dispensed from the cassette.


In a further preferred embodiment of the invention the cassette comprises a malodor counteractant useful for absorbing, adsorbing or masking the smell of the waste.


In a preferred embodiment of the invention the film inside the cassette the film is in compressed configuration.


Seal Apparatus


A preferred version of the sealing apparatus of the present invention is an apparatus capable of impulse sealing. An impulse sealer is a jaw sealer backed with resilient silicone rubber. Electric current flows through Nichrome ribbon stretched over one over one or both surfaces and covered with high temperature release film and fabric.


Another preferred version of the seal apparatus is wire or knife sealing. According to this method a hot wire or knife seals and cuts the film.


Other methods for the seal apparatus that could be used according to the invention include bar sealing, band sealing, ultrasonic sealing, friction sealing, gas sealing, contact sealing, hot melt sealing, pneumatic sealing, dielectric sealing, magnetic sealing, induction sealing, radiant sealing, solvent sealing etc. For these methods please refer to the Wiley Encyclopedia of packaging technology, edition 1997.


In a preferred embodiment of the invention the electric current necessary for the heat sealing and fusion is provided through a rechargeable battery. The voltage of the rechargeable battery is preferably equal or less than 20 V, even more preferably less than 16 V, even more preferably less than 12V.


In a preferred version of the invention the temperature for the heat seal is less than 100° C., preferably less than 90° C., preferably less than 80° C.


In a further preferred version of the invention, the sealing time is less than 5 seconds, more preferably less than 3 seconds, more preferably less than 1 second.


In a further preferred version of the invention, the cutting of each pack to the previous one is done simultaneously with the sealing by the use of a wire/knife configuration. In another version, there is no cutting. In this case all the packs are put together inside the bin in a single line.


The use of a rechargeable battery of low voltage assures a safe procedure that is more user friendly than household electricity.


Another alternative possibility of the invention is the use of more than one heat seal to make an individual pack. So two, three or four seals are possible.


In the case of three or four seals, the film should be in a “single sheet” configuration instead of “flexible tubing”.


In FIG. 2 there is further explanation of the sealing apparatus. The two sealing jaws (see reference number 23) are heat sealing the flexible tubular film. The sealing jaws are movable on a railway (see reference number 22) and the movement is controlled through as gear reducer (see reference number 21). This is also displayed in FIG. 3 from another view.


The activation of the sealing mechanism can be done by the person using the apparatus preferably by pushing an activation mechanism (eg a button or a lever) either by hand or by foot. The activation mechanism provokes by preferably mechanical or pneumatic transmission system the movement of the sealing jaws therefore allowing the fusion seal to occur. Electrical transmission is also possible by using a battery as a source of power.


Film Characteristics


The basic characteristics a film should have in order to be used in the particular case are

    • 1. Barrier to odours
    • 2. To have the proper deadfold properties (non resilient) so that is compressed efficiently in the cassette if a cassette is used as a dispensing apparatus.
    • 3. To have sufficient mechanical properties (eg tensile strength at break, elongation).
    • 4. To have sufficient sealing properties as to be sealed with a low voltage rechargeable battery. Also the sealing properties must be sufficient to seal through wrinkles or pleats that are inevitable for this kind of application.


We have surprisingly found that all these features can be achieved with a very lightweight multilayer film with weight per surface ratio less than 20 grams per square meter, preferably less than 18 grams per square meter. This is extremely beneficial for the environment as multilayer films are extremely difficult to be produced with so small weight per surface.


In order for a film to be able to heat seal hermetically to itself or to other film with the power generated by a low voltage battery and also be able to keep the other critical characteristics (odour barrier, sealability through pleats and wrinkles, mechanical strength) it should combine the following characteristics:

    • 1. Comprise an internal layer comprising at least one oxygen barrier material
    • 2. Comprise one outer layer comprising more than 50% per weight polyethylene homopolymer and/or copolymer and one inner layer comprising more than 50% per weight polyethylene homopolymer and/or copolymer
    • 3. Have a weight/surface ratio of less than 20 grams per square meter.
    • 4. The film can be heat sealed with the thermal energy transferred with a battery with a voltage of equal or less than 20 V.


According to a further aspect the present invention is directed to a multilayer film with weight less than 15 g/m2 which:

    • 1. Comprises a layer comprising at least one oxygen barrier material
    • 2. Comprise one outer layer comprising more than 50% per weight polyethylene homopolymer and/or copolymer and one inner layer comprising more than 50% per weight polyethylene homopolymer or copolymer
    • 3. The film can be heat sealed with the thermal energy transferred with a battery with a voltage of equal or less than 20 V.


According to a further aspect the present invention is directed to a multilayer film with weight less than 13 g/m2 which:

    • 1. comprises a high oxygen barrier layer comprising at least one oxygen barrier material
    • 2. comprise two outer layers comprising more than 50% per weight polyethylene homopolymer or copolymer
    • 3. the film can be heat sealed with the thermal energy transferred with a battery with a voltage of equal or less than 20 V.


In a further preferred embodiment, the film comprises the construction:


Outer Layer/Abuse Layer/Intermediate Layer/Barrier Layer/Intermediate Layer/Abuse Layer/Inner Layer


In another preferred embodiment, the film comprises the construction


Outer Layer/Intermediate Layer/Barrier Layer/Intermediate Layer/Inner Layer


Detailed Description of Layers:


Barrier (Internal) Layer


In a preferred version of the invention, the oxygen barrier material in the barrier (internal) layer is EVOH, PVDC or polyamide. The EVOH used preferably has an ethylene content less than 48%, more preferably less than 44%, more preferably less than 38%, more preferably from 27 to 32% ethylene.


The oxygen barrier material preferably has a weight of less than 3 g/m2, more preferably less than 2 g/m2 and even more preferably less than 1.5 g/m2.


Outer Layer


In a preferred version, the outer layer comprises at least 50% per weight polyethylene homopolymer or copolymer.


In a further preferred version, the weight of the outer layer is less than 6 g/m2, more preferably less than 5 g/m2.


In a further preferred version, the polyethylene is a copolymer or a blend of different monomers or polymeric structures. This blending may take place during polymerization or as a later stage.


In a further preferred version the polyethylene is a copolymer of ethylene and butene or a copolymer of ethylene and hexene or a copolymer of ethylene and octene.


In a further preferred version the polyethylene has a density of between 0.885 and 0.960 g/m3, more preferably 0.910 to 0.940 g/m3.


Inner Layer


Preferred materials for the inner layer include polyethylene homopolymer or copolymers, such as low density polyethylene, high density polyethylene, ethylene ester copolymer, ethylene alpha olefin copolymer and ethylene propylene copolymers. Ethylene based ionomers and ethylene styrene copolymers are also possible. Ethylene alpha olefin copolymer is particularly preferred.


According to a further embodiment, the present invention is of the same configuration where the inner layer comprises a “substantially non resilient material” (SNR).


In a preferred version of the invention, the SNR material is at least 10 percent, preferably at least 20, preferably at least 30 percent per weight of the inner layer.


Intermediate Layer


In the intermediate layers, typical adhesive resins like maleic anhydrite modified polyolefins may be used. Typical examples are BYNEL from Dupont and OREVAC from Arkema.


In another preferred version of the invention, polyamide could be used as intermediate layer.


Abuse Layer


In a multilayer configuration where abuse layers are also present, these layers may comprise polyethylene and polypropylene homopolymers or copolymers. Polyamides are also possible.


General


Additives well known in the art may be used in one or more layers of the present invention. Slip additives, antiblock additives, antifog, polymer processing aids may be used if pertinent. Antimicrobial additives may also be used in one or more of the layers to inhibit the microbe formation. Preferably the antimicrobial is put on the side where the waste is in direct vicinity.


In order to increase the mechanical properties the film may be crosslinked with one of the following methods.


E-beam radiation, gamma radiation, moisture crosslinking using silane grafting compounds, peroxide crosslinking.


The film may be in tubular form or sealed at the edges or single sheet configuration. Centrefold configuration is also possible.


The preferred production method for the film is the hot blown film method, which is well known in the art. Other methods like extrusion through flat cast die is also possible. The hot blown film method allows orientation of the plastic from the melt state. Biaxiallly oriented film such as those produced by double bubble or tenter frame method are not really efficient for the application during the much higher complexity of the process which renders the production cost much higher.


As outlined above, the inner and outer layers of the present invention are substantially free of “cling” additives meaning additives that allow the layer adhere to itself by pressing force without the need of fusion seal. Addition of such additives is costly and complicated. Also it makes the whole process much less friendly due to the tacky nature of the cling additive.


EXAMPLES

A 5 layer film is produced in a commercial hot blown film line with the following recipe


Inner layer, 80% EAO1+15% SNR1+5% ADDITIVES


Adjacent layer 100% ADH 1


Barrier layer EVOH 1


Adjacent layer 100% ADH1


Outer layer 100% EAO1


See table 1


The thickness of the structure is 4/1.5/1.5/1.5/4 starting from the inner and going to the outer layer. The weight of the film is 12.145 g/m2.













TABLE 1









Density



Type
Description
g/cm3




















EAO1
Ethylene octene
0.92




copolymer



SNR1
Calcium
1.6




carbonate




compound



AD1
LLDPE mod.
0.92




Adhesive tie



EVOH 1
EVOH with 32%
1.19




ethylene



EVOH 2
EVOH with 29%
1.2




ethylene










Example 2

A 5 layer film is produced in a hot blown film commercial line with the following recipe


Inner layer, 80% EAO1+15% SNR1+5% ADDITIVES


Adjacent layer 100% ADH 1


Barrier layer EVOH 2


Adjacent layer 100% ADH1


Outer layer 80% EAO1+15% SNR1+5% ADDITIVES


The thickness of the structure is 5/1.5/1.5/1.5/3 starting from the inner and going to the outer layer.


The weight of the material is 12.385 g/m2.


Example 3

A 5 layer film is produced in a hot blown film commercial line with the following recipe


Inner layer, 80% EAO1+15% SNR1+5% ADDITIVES


Adjacent layer 100% ADH 1


Barrier layer EVOH 2


Adjacent layer 100% ADH1


Outer layer 80% EAO1+15% SNR1+5% ADDITIVES


The thickness of the structure is 5/3/1.5/3/5 starting from the inner and going to the outer.


The weight of the material is 17.1 g/m2.


Tests






    • 1. Tensile strength and elongation test is done according to ASTM D 882.

    • 2. Odour test is done in the way described below.


      Test 1.





Tensile strength and elongation is measured as per ASTM D882.


MD stands for machine direction, whereas TD stands for transverse direction.

















TENSILE
ELONGA-
TENSILE
ELONGA-



STRENGTH
TION
STRENGTH
TION


EXAMPLE
(MD)
(MD)
(TD)
(TD)



















1
22
250
21
630


2
21
225
19.8
550


3
25
190
23
520










Odour Testing


10 soiled diapers are put in a film of the present invention and also in a commercially sold film. The commercially sold film is believed to be monolayer.


The packs are put in PVDC comprising bags, so the odour cannot escape during the time of the evaluation.


The bags are opened 3 days after the soiling of the diapers and smell was evaluated by a 5 member panel.


The packs made from examples 1 and 2 were found substantially less smelly than the commercially sold ones.


Sealing Testing


The sealing testing was done in comparison with a commercial film specialized for the particular application with a weight/surface ratio of 21.9 g/m2. For the testing two sealing jaws that used the energy produced by a battery of 20 V were used.


It was surprisingly found that the film of examples 1, 2 and 3 were able to seal efficiently even through wrinkles with the sealing apparatus. On the other hand, the film of 21.9 g/m2 was not able to seal efficiently. If the sealing time was increased (something which is not desirable according to the invention) the seal was “burned”.

Claims
  • 1. A method for storing waste by using a device comprising (i) a dispensing apparatus where a plastic film of weight/surface ratio less than 20 grams per square meter is stored; (ii) a fusion seal apparatus comprising a battery with a maximum voltage of equal to or less than 20 V; and (iii) a bin where the fusion seal apparatus is located; the method comprising: a. pulling out the plastic film of weight/surface ratio less than 20 grams per square meter from the dispensing apparatus;b. putting a waste item in a suitable length of the plastic film; andc. closing hermetically the plastic film with the use of the fusion seal apparatus to provide a seal between a part of the plastic film and another part of the same plastic film, where the sealed parts are put sequentially in the bin.
  • 2. A plastic film for use in the method according to claim 1, comprising at least an outer layer comprising at least 50% per weight polyethylene homopolymer and/or copolymer, where the weight/surface ratio of the plastic film is less than 20 grams per square meter and where the plastic film can be heat sealed with the thermal energy transferred with the battery with the voltage of equal to or less than 20 V.
  • 3. The plastic film of claim 2, further comprising an internal layer comprising at least one oxygen barrier material and/or a sealing layer comprising at least 50% per weight polyethylene homopolymer and/or copolymer, wherein the sealing layer is a layer configured to be sealed using the fusion seal apparatus, and wherein the internal layer is a film layer located between other layers of the plastic film.
  • 4. The plastic film of claim 2, comprising a sealing layer comprising at least 50% per weight polyethylene homopolymer and/or copolymer.
  • 5. The plastic film of claim 2, where the weight/surface ratio is less than 15 g/m2.
  • 6. The plastic film of claim 2, where the weight/surface ratio is less than 13 g/m2.
  • 7. The plastic film of claim 2, comprising an internal layer comprising an oxygen barrier material, where the oxygen barrier material is EVOH, PVDC or polyamide.
  • 8. The plastic film of claim 2, where the polyethylene copolymer is selected from the group consisting of a copolymer of ethylene and butene, a copolymer of ethylene and hexene, and a copolymer of ethylene and octene.
  • 9. A plastic film for use in the method according to claim 1 comprising at least an outer layer comprising polyethylene homopolymer and/or copolymer;a sealing layer comprising polyethylene homopolymer and/or copolymer; andan internal layer located between the outer layer and the sealing layer, wherein said internal layer comprises at least one oxygen barrier material;where the weight/surface ratio of the plastic film is less than 20 grams per square meter and where the plastic film can be heat sealed with the thermal energy transferred with the battery with the voltage of equal to or less than 20 V.
  • 10. The plastic film of claim 9, wherein the outer and/or sealing layer comprise at least 50% per weight polyethylene homopolymer and/or copolymer.
  • 11. The plastic film of claim 9, where the weight/surface ratio is less than 15 g/m2.
  • 12. The plastic film of claim 9, where the weight/surface ratio is less than 13 g/m2.
  • 13. The plastic film of claim 9, where the oxygen barrier material is EVOH, PVDC or polyamide.
  • 14. The plastic film of claim 9, where the polyethylene copolymer is selected from the group consisting of a copolymer of ethylene and butene, a copolymer of ethylene and hexene, and a copolymer of ethylene and octene.
Priority Claims (2)
Number Date Country Kind
11164527 May 2011 EP regional
11166232 May 2011 EP regional
Parent Case Info

The present U.S. patent application is a divisional application of U.S. patent application Ser. No. 13/157,876, filed Jun. 10, 2011, which claims priority to European Patent Application No. 11 164 527.1, filed May 3, 2011, and European Patent Application No. 11 166 232.6, filed May 16, 2011. The disclosure of each of these applications is incorporated herein by reference in its entirety.

US Referenced Citations (173)
Number Name Date Kind
2380054 Lautmann Aug 1943 A
2376185 Randall May 1945 A
3214884 Langdon Nov 1965 A
3299194 Golike Jan 1967 A
3456044 Pahlke Jul 1969 A
3536192 Couper Oct 1970 A
3846569 Kaplan Nov 1974 A
3908336 Forslund Sep 1975 A
3956229 Bollen et al. May 1976 A
4064296 Bornstein et al. Dec 1977 A
4207363 Lustig Jun 1980 A
4207364 Nyberg Jun 1980 A
4254869 Heier Mar 1981 A
4362834 Lefevre et al. Dec 1982 A
4399181 Yoshimura et al. Aug 1983 A
4595433 Ford et al. Jun 1986 A
4612221 Biel et al. Sep 1986 A
4619849 Anzawa et al. Oct 1986 A
4650721 Ashcraft et al. Mar 1987 A
4705707 Winter Nov 1987 A
4716061 Winter Dec 1987 A
4786561 Fong Nov 1988 A
4801486 Quacquarella et al. Jan 1989 A
4857399 Vicik Aug 1989 A
4863769 Lustig et al. Sep 1989 A
4869049 Richards et al. Sep 1989 A
4879430 Hoffman Nov 1989 A
4911979 Nishimoto et al. Mar 1990 A
4912149 Robeson et al. Mar 1990 A
4934529 Richards et al. Jun 1990 A
4941310 Kristen Jul 1990 A
4948657 Ogawa et al. Aug 1990 A
4976898 Lustig et al. Dec 1990 A
4977022 Mueller Dec 1990 A
4990562 Chou et al. Feb 1991 A
5001192 Sun Mar 1991 A
5034281 Kawasaki et al. Jul 1991 A
5079051 Garland et al. Jan 1992 A
5092105 Bish-Shin Mar 1992 A
5142123 Chou Aug 1992 A
5169708 Amaral et al. Dec 1992 A
5179168 Hirasawa Jan 1993 A
5256351 Lustig et al. Oct 1993 A
5256428 Lustig et al. Oct 1993 A
5296580 Matsunaga et al. Mar 1994 A
5298202 Schirmer Mar 1994 A
5302402 Dudenhoeffer et al. Apr 1994 A
5350788 Visioli et al. Sep 1994 A
5358792 Mehta et al. Oct 1994 A
5382470 Vicik Jan 1995 A
5397613 Georgelos Mar 1995 A
5562958 Walton et al. Oct 1996 A
5593747 Georgelos Jan 1997 A
5645788 Bekele Jul 1997 A
5698279 Vicik Dec 1997 A
5834077 Babrowicz Nov 1998 A
5837335 Babrowicz Nov 1998 A
5851610 Ristey et al. Dec 1998 A
5888615 Mascarenhas et al. Mar 1999 A
5983607 Mihalov et al. Nov 1999 A
6013378 White et al. Jan 2000 A
6058998 Kristen May 2000 A
6065272 Lecomte May 2000 A
6074715 Lind et al. Jun 2000 A
6088996 Maruyama Jul 2000 A
6146726 Yoshii et al. Nov 2000 A
6220753 Metzger Apr 2001 B1
6221410 Ramesh et al. Apr 2001 B1
6258423 Giori Jul 2001 B1
6274246 Eggers et al. Aug 2001 B1
6299984 Forloni Oct 2001 B1
6346285 Ramesh Feb 2002 B1
6406763 Wolf et al. Jun 2002 B1
6458437 Ito et al. Oct 2002 B1
6506463 Cahill et al. Jan 2003 B1
6514583 Ahlgren et al. Feb 2003 B1
6516588 Jensen et al. Feb 2003 B2
6531198 Lind et al. Mar 2003 B2
6534137 Vadhar Mar 2003 B1
6558760 Paleari May 2003 B1
6572959 Buongiorno et al. Jun 2003 B1
6592975 Ueyama et al. Jul 2003 B1
6610046 Usami et al. Aug 2003 B1
6663905 Ennis et al. Dec 2003 B1
6682792 Schmal et al. Jan 2004 B2
6682825 Kennedy Jan 2004 B1
6777046 Tatarka et al. Aug 2004 B1
6869686 Idlas Mar 2005 B1
6960635 Stevens et al. Nov 2005 B2
6984695 Brown et al. Jan 2006 B2
7473473 Verrocchi Jan 2009 B2
7611770 Kennedy et al. Nov 2009 B2
7736726 McAllister et al. Jun 2010 B2
8129006 Ginossatis Mar 2012 B2
8697211 Gkinosatis Apr 2014 B2
9290320 Gkinosatis Mar 2016 B2
9365687 Gkinosatis Jun 2016 B2
9440778 Prater et al. Sep 2016 B2
9440788 Gkinosatis Sep 2016 B2
9604430 Gkinosatis Mar 2017 B2
9789669 Gkinosatis Oct 2017 B2
20020038535 Jensen Apr 2002 A1
20020066261 Richards Jun 2002 A1
20020119334 Shepard et al. Aug 2002 A1
20020172834 Rivett et al. Nov 2002 A1
20030008084 Vicik Jan 2003 A1
20030012900 Wolf et al. Jan 2003 A1
20030073785 Okada et al. Apr 2003 A1
20030124452 Nair et al. Jul 2003 A1
20030131569 Chomik et al. Jul 2003 A1
20030213804 Chomik et al. Nov 2003 A1
20030218022 Chomik et al. Nov 2003 A1
20030220453 Ebara et al. Nov 2003 A1
20040020175 Stravitz Feb 2004 A1
20040020913 Hovorka Feb 2004 A1
20040043238 Wuest et al. Mar 2004 A1
20040048086 Kennedy et al. Mar 2004 A1
20040065052 Ramesh et al. Apr 2004 A1
20040074904 Share et al. Apr 2004 A1
20040157077 Roussos Aug 2004 A1
20040159972 Koschmieder et al. Aug 2004 A1
20040194433 Chomik et al. Oct 2004 A1
20050044819 Chomik et al. Mar 2005 A1
20050064123 Chomik et al. Mar 2005 A1
20050079372 Schmal et al. Apr 2005 A1
20050129811 Kraimer et al. Jun 2005 A1
20050147778 Tai et al. Jul 2005 A1
20050191439 Hirose et al. Sep 2005 A1
20050235611 Roussos Oct 2005 A1
20050239961 Saraf et al. Oct 2005 A1
20050271877 Ginossatis Dec 2005 A1
20060010837 Jurus Jan 2006 A1
20060172143 Breese et al. Aug 2006 A1
20060177616 Barber et al. Aug 2006 A1
20060177641 Breese et al. Aug 2006 A1
20060199030 Liang et al. Sep 2006 A1
20060199911 Markovich et al. Sep 2006 A1
20060199912 Fuchs et al. Sep 2006 A1
20060254219 Alipour et al. Nov 2006 A1
20060272767 Kreitman et al. Dec 2006 A1
20060283153 Nakano Dec 2006 A1
20060286323 Siegel et al. Dec 2006 A1
20070042089 Grah Feb 2007 A1
20070082150 Ginossatis Apr 2007 A1
20070089688 Nitzsche et al. Apr 2007 A1
20070178285 Rasanen et al. Aug 2007 A1
20080003332 Ginossatis et al. Jan 2008 A1
20080070047 Rehkugler et al. Mar 2008 A1
20080095960 Schell et al. Apr 2008 A1
20080115463 Wilson May 2008 A1
20080255311 Chang et al. Oct 2008 A1
20080274314 Gkinosatis Nov 2008 A1
20080274328 Gkinosatis Nov 2008 A1
20080305220 Gkinosatis Dec 2008 A1
20090013656 Nasiatka et al. Jan 2009 A1
20090034886 Conforti Feb 2009 A1
20090176117 Gkinosatis Jul 2009 A1
20090191392 Gkinosatis Jul 2009 A1
20090196962 Gkinosatis Aug 2009 A1
20090240227 Toro et al. Sep 2009 A1
20090263599 Gkinosatis Oct 2009 A1
20100028574 Gkinosatis Feb 2010 A1
20100032098 Lalli et al. Feb 2010 A1
20100034939 Gkinosatis Feb 2010 A1
20100221391 Deng et al. Sep 2010 A1
20110159263 Gkinosatis Jun 2011 A1
20120279181 Gkinosatis Nov 2012 A1
20120289645 Tice et al. Nov 2012 A1
20130019568 Gkinosatis Jan 2013 A1
20130209797 Gkinosatis Aug 2013 A1
20130227916 Gkinosatis Sep 2013 A1
20150010764 Gkinosatis Jan 2015 A1
20150210454 Gkinosatis Jul 2015 A1
Foreign Referenced Citations (67)
Number Date Country
511 195 Jul 1980 AU
0 005 660 Nov 1979 EP
0 286 407 Oct 1988 EP
0 402 043 Dec 1990 EP
0 472 418 Feb 1992 EP
0 627 465 Dec 1994 EP
0 686 497 Dec 1995 EP
0 810 087 Dec 1997 EP
1 072 632 Jan 2001 EP
0 930 349 Jun 2003 EP
1 060 077 Jun 2003 EP
1 131 205 Dec 2004 EP
1 514 680 Mar 2005 EP
1 415 930 Apr 2006 EP
1 770 116 Apr 2007 EP
1 854 625 Nov 2007 EP
08162162.5 Aug 2008 EP
1 985 440 Oct 2008 EP
1 985 443 Oct 2008 EP
1 995 058 Nov 2008 EP
2 077 239 Jul 2009 EP
2 077 297 Jul 2009 EP
2 085 216 Aug 2009 EP
2 111 979 Oct 2009 EP
2 147 783 Jan 2010 EP
2 194 006 Jun 2010 EP
2 332 723 Jun 2011 EP
2 520 518 Nov 2012 EP
792290 Mar 1958 GB
1 140 765 Jan 1969 GB
2 203 326 Oct 1988 GB
2 236 531 Apr 1991 GB
62107810 May 1987 JP
03 200534 Sep 1991 JP
07196818 Aug 1995 JP
07206004 Aug 1995 JP
07206005 Aug 1995 JP
07206006 Aug 1995 JP
2002-234975 Aug 2002 JP
2003-159761 Jun 2003 JP
2005-047959 Feb 2005 JP
2005-335111 Dec 2005 JP
2006-247870 Sep 2006 JP
567768 Nov 2009 NZ
567767 May 2010 NZ
WO1996001736 Jan 1996 WO
WO 9712758 Apr 1997 WO
WO1997046384 Dec 1997 WO
WO1998021274 May 1998 WO
WO1998021276 May 1998 WO
WO1999044824 Sep 1999 WO
WO1999057612 Nov 1999 WO
WO2000061439 Oct 2000 WO
WO0063085 Dec 2000 WO
WO2001023268 Apr 2001 WO
WO2002026493 Apr 2002 WO
WO2003020515 Mar 2003 WO
WO 2003061959 Jul 2003 WO
WO2006053885 May 2006 WO
WO2006075141 Jul 2006 WO
WO 2006076393 Jul 2006 WO
WO2006102152 Sep 2006 WO
WO2007053603 May 2007 WO
WO2008091321 Jul 2008 WO
WO2008118554 Oct 2008 WO
WO 2009052291 Apr 2009 WO
WO 2011029597 Mar 2011 WO
Non-Patent Literature Citations (159)
Entry
“15.13xEA—Ethylene Vinyl Acetate (EVA) Copolymers (>50% Ethylene)—European Adhesives,” The ChemQuest Group, Inc. http://web.archive.org/web/20080219220919/http://www.chemquest.com/store/ethylene-vinyl-acetate-copolymers-european-adhesives.html (Aug. 26, 2011) (2 pages).
“Baymod L 2450,” Product Data Sheet, LANXESS. (2 pages) (2007).
“DuPontTM Elvax® 3170,” DuPont Packaging & Industrial Polymers. 3 pages(2004) http://web.archive.org/web/20060516114601/http://www2.dupont.com/Elvax/en_US/assets/downloads/vax3170.pdf.
“Elvaloy resins,” Product Data Sheet, DuPont Packaging & Industrial Polymers. (2 pages) (2010).
“Filling and sealing of containers” in Fellows, P.J. (2000). Food Processing Technology—Principles and Practice (2nd Edition). Woodhead Publishing.
“Polybutylene terephthalate,” Britcannica Online Encyclopedia. pp. 1-3 (Accessed on Sep. 7, 2011) <http://www.britannica.com/EBchecked/topic/468341/polybutylene-terephthalate-PBT>.
“Polybutylene terephthalate (PBT),” 1 page <http://www.britannica.com/EBchecked/topic/468341/polybutylene-terephthalate-PBT> (Accessed on Jun. 13, 2012).
“Polymer Blend,” IUPAC Compendium of Chemical Terminology. 2nd Edition (1997).
Advisory Action corresponding to U.S. Appl. No. 12/319,150 dated Nov. 13, 2013.
Advisory Action corresponding to U.S. Appl. No. 11/801,609 dated Jun. 16, 2016.
Annonymous, “Advantages of metallocene ethylene [olymer resins in multilayer stretch films,” Research Disclosure, Mason Publications, Hampshire, GB. vol. 419, No. 26 (1999).
Annonymous, “Some benefits from the use of metallocene ethylene polymers in blown and cast films,” Research Disclosure, Mason Publications, Hampshire, GB. vol. 392, No. 54 (1996).
ASTM D 1003-07 “Haze and Luminous Transmittance of Transparent Plastics,” ASTM International. pp. 1-7.
ASTM D 1525-07 “Vicat Softening Temperature of Plastics,” ASTM International. pp. 1-9.
ASTM D 2732-03 “Unrestrained Linear Thermal Shrinkage of Plastic Film and Sheeting,” ASTM International. pp. 1-5.
ASTM D3418-08. Standard Test Method for Transition Temperatures and Enthalpies of Fusion and Crystallization of Polymers by Differential Scanning Calorimetry. American National Standards Institute. Dec. 2008. www.astm.org.
ASTM D3985. Standard Test Method for Oxygen Gas Transmission Rate Through Plastic Film and Sheeting Using a Coulometric Sensor. American National Standards Institute. pp. 1-7. www.astm.org.
ASTM D882-09. Standard Test Method for Tensile Properties of Thin Plastic Sheeting. American National Standards Institute. Jan. 2009. www.astm.org.
ASTM F1927-07. Standard Test Method for Determination of Oxygen Gas Transmission Rate, Permeability and Permeance at Controlled Relative Humidity Through Barrier Materials Using a Coulometric Detector. American National Standards Institute. Aug. 2007. www.astm.org.
BS 2782-0:2004 “Methods of Testing Plastics,” British Standards Institution. pp. 1-29 (2004).
English abstract of JP 2005-103902, USUI, Apr. 2005.
European Search Report corresponding to European Patent Application No. 08173057.4-2307 dated Sep. 22, 2009.
European Search Report corresponding to European Patent Application No. 08173056.6-2109 dated Mar. 16, 2009.
Extended European Search report corresponding to European Patent Application No. 09151289.7-2124 dated Jun. 8, 2009.
Extended European Search Report corresponding to European Patent Application No. 05021541.7-2115 dated Dec. 2, 2005.
Extended Eurpoean Search Report corresponding to European Patent Application No. 08156814 dated Oct. 9, 2008.
Extended European Search Report corresponding to European Patent Application No. 08154742.4-2124 dated Jul. 2, 2009.
Extended European Search Report corresponding to European Patent Application No. 10193414.9-1217 dated May 9, 2011.
Harper, “Modern Plastics Handbook.” McGraw-Hill: New York, New York. pp. 3.17-3.22 (2000).
Hough, M., and Dolbey, R., “Modern Plastics Compendium, vol. 1—Key Properties and Sources,” Smithers Rapra Technology. pp. 87-124 (1995).
Huskić, M., and {hacek over (S)}ebenik, A., “Characterization of Crosslinked Ethylene-Vinylacetate Copolymers,” Polymer International. vol. 31, No. 1, pp. 41-44 (1993).
Interview Summary corresponding to U.S. Appl. No. 11/801,609 dated Jul. 31, 2012.
Interview Summary corresponding to U.S. Appl. No. 12/150,261 dated Dec. 28, 2010.
Interview Summary corresponding to U.S. Appl. No. 12/150,261 dated Sep. 21, 2011.
Interview Summary corresponding to U.S. Appl. No. 12/150,261 dated Jun. 12, 2012.
Interview Summary corresponding to U.S. Appl. No. 12/319,149 dated Oct. 17, 2011.
Interview Summary corresponding to U.S. Appl. No. 12/319,149 dated Jun. 15, 2012.
Interview Summary corresponding to U.S. Appl. No. 12/319,150 dated Sep. 23, 2011.
Interview Summary corresponding to U.S. Appl. No. 12/319,150 dated Sep. 6, 2013.
Interview Summary corresponding to U.S. Appl. No. 12/322,347 dated Sep. 21, 2011.
Interview Summary corresponding to U.S. Appl. No. 12/508,233 dated Apr. 26, 2012.
Interview Summary corresponding to U.S. Appl. No. 13/722,323 dated Jan. 22, 2016.
Kipp, “Plastic Material Data Sheets,” MatWeb (2004) (5 pages).
Machine Translation of JP 2005-103902, USUI, Apr. 2005.
Notice of Allowance corresponding to U.S. Appl. No. 11/528,741 dated Oct. 28, 2011.
Notice of Allowance corresponding to U.S. Appl. No. 12/150,168 dated Nov. 25, 2013.
Notice of Allowance corresponding to U.S. Appl. No. 13/157,876 dated Nov. 12, 2015.
Notice of Allowance corresponding to U.S. Appl. No. 12/319,150 dated Feb. 12, 2016.
Notice of Allowance corresponding to U.S. Appl. No. 13/523,462 dated May 16, 2016.
Notice of Publication of Application for U.S. Appl. No. 14/946,169 dated Jun. 23, 2016.
Official action corresponding to European Patent Application No. 10 193 414.9-1303 dated Oct. 29, 2014.
Official Action corresponding to New Zealand Patent Application No. 626181 dated Jun. 18, 2014.
Official Action corresponding to United Kingdom Patent Application No. GB1020302.4 dated Jul. 2, 2014.
Official Action corresponding to United Kingdom Patent Application No. GB1020302.4 dated Dec. 11, 2014.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Sep. 15, 2009.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Feb. 5, 2010.
Official Action corresponding to U.S. Appl. No. 12/150,261 dated Oct. 27, 2009.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Oct. 15, 2009.
Official Action corresponding to U.S. Appl. No. 11/528,741 dated Mar. 30, 2010.
Official Action corresponding to U.S. Appl. No. 12/150,261 dated Jul. 7, 2010.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Jul. 7, 2010.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Jul. 15, 2010.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Sep. 14, 2010.
Official Action corresponding to U.S. Appl. No. 12/319,150 dated Oct. 15, 2010.
Official Action corresponding to U.S. Appl. No. 11/528,741 dated Jan. 4, 2011.
Official Action corresponding to U.S. Appl. No. 12/508,233 dated Mar. 9, 2011.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Feb. 16, 2011.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Mar. 16, 2011.
Official Action corresponding to U.S. Appl. No. 12/150,261 dated Mar. 22, 2011.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Mar. 22, 2011.
Official Action corresponding to U.S. Appl. No. 12/154,662 dated Mar. 29, 2011.
Official Action corresponding to U.S. Appl. No. 12/319,150 dated Apr. 26, 2011.
Official Action corresponding to U.S. Appl. No. 11,528,741 dated May 18, 2011.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Jun. 20, 2011.
Official Action corresponding to U.S. Appl. No. 12/154,662 dated Aug. 18, 2011.
Official Action corresponding to U.S. Appl. No. 12/154,662 dated Jan. 18, 2012.
Official Action corresponding to U.S. Appl. No. 12/512,361 dated Aug. 31, 2011.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Sep. 23, 2011.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Oct. 26, 2011.
Official Action corresponding to U.S. Appl. No. 12/319,150 dated Nov. 4, 2011.
Official Action corresponding to U.S. Appl. No. 12/508,233 dated Nov. 23, 2011.
Official Action corresponding to U.S. Appl. No. 12/508,233 dated Jun. 6, 2012.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Dec. 2, 2011.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Jan. 17, 2012.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Jan. 30, 2012.
Official Action corresponding to U.S. Appl. No. 12/150,261 dated Jan. 31, 2012.
Official Action corresponding to U.S. Appl. No. 12/426,496 dated Feb. 7, 2012.
Official Action corresponding to U.S. Appl. No. 12/512,361 dated May 2, 2012.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated May 15, 2012.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Aug. 14, 2012.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Aug. 27, 2012.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Sep. 25, 2012.
Official Action corresponding to U.S. Appl. No. 12/319,150 dated Mar. 14, 2013.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Apr. 26, 2013.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Jul. 24, 2013.
Official Action corresponding to U.S. Appl. No. 13/157,876 dated Nov. 19, 2013.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Nov. 29, 2013.
Official Action corresponding to U.S. Appl. No. 13/722,323 dated Mar. 27, 2014.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Apr. 24, 2014.
Official Action corresponding to U.S. Appl. No. 13/157,876 dated Jun. 2, 2014.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Aug. 1, 2014.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Sep. 24, 2014.
Official Action corresponding to U.S. Appl. No. 13/722,323 dated Jan. 7, 2015.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Jan. 7, 2015.
Official Action corresponding to U.S. Appl. No. 13/523,462 dated Jan. 30, 2015.
Official Action corresponding to U.S. Appl. No. 13/157,876 dated Mar. 3, 2015.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated May 20, 2015.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Jun. 12, 2015.
Official Action corresponding to U.S. Appl. No. 13/682,160 dated Jun. 15, 2015.
Official Action corresponding to U.S. Appl. No. 13/722,323 dated Jul. 17, 2015.
Official Action corresponding to U.S. Appl. No. 12/319,150 dated Jul. 22, 2015.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Sep. 16, 2015.
Official Action corresponding to U.S. Appl. No. 13/523,462 dated Sep. 21, 2015.
Official Action corresponding to U.S. Appl. No. 14/612,175 dated Dec. 9, 2015.
Official Action corresponding to U.S. Appl. No. 13/682,160 dated Jan. 29, 2016.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Feb. 2, 2016.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Feb. 18, 2016.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Mar. 31, 2016.
Official Action corresponding to U.S. Appl. No. 13/722,323 dated May 3, 2016.
Official Action corresponding to U.S. Appl. No. 13/682,160 dated Jun. 30, 2016.
Official Action corresponding to U.S. Appl. No. 14/304,101 dated Jun. 30, 2016.
Petrie, “Handbook of Adhesives and Sealants,” 2nd Edition. McGraw-Hill: New York, New York. pp. 465-466 (2007).
“Polymer Materials Selection for Radiation-Sterilized Products.” <http://www.mddionline.com/article/polymer-materials-selection-radiation-sterilized-products> dated Feb. 1, 2000.
Search Report corresponding to French Patent Application No. 1059997 dated Jan. 16, 2012.
Unisource—Moisture Barrier & Oxygen Barrier Transmission Rates; <http://www.unisourcelink.com/packaging/pdf/MoistureBarrier.pdf> (Retrieved on Jan. 10, 2012).
Advisory Action, Examiner Initiated Interview Summary, and AFCP 2.0 Decision corresponding to U.S. Appl. No. 14/612,175 dated Jan. 4, 2017.
Interview Summary corresponding to U.S. Appl. No. 13/682,160 dated Oct. 28, 2016.
Kerns, “What's the Difference Between Batteries and Capacitors?” Machine Design, Batteries/Power Supplies, pp. 1-4 (May 11, 2015).
Notice of Allowance corresponding to U.S. Appl. No. 13/722,323 dated Nov. 18, 2016.
Notice of Decision form Post-Prosectuion Pilot Program (P3) Conference corresponding to U.S. Appl. No. 12/957,947 dated Dec. 14, 2016.
Official Action corresponding to U.S. Appl. No. 14/612,175 dated Aug. 5, 2016.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Aug. 17, 2016.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Sep. 26, 2016.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Nov. 16, 2016.
Official Action corresponding to U.S. Appl. No. 14/304,101 dated Dec. 9, 2016.
Official Action corresponding to U.S. Appl. No. 13/682,160 dated Mar. 2, 2017.
Pish, “Ragone Plot,” 2016 Advisory Panel Energy Storage, Center for Electromechanics, The University of Texas at Austin https://utw10356.utweb.utexas.edu/sites/default/files/Pish.pdf, p. 1, (May 10, 2016).
“Ragone Chart,” Wikipedia, http://en.wikipedia.org/wiki/Ragone_chart, pp. 1-2, downloaded Dec. 21, 2016.
Scherson et al., “Batteries and Electrochemical Capacitors,” The Electricochemical Society Interface, pp. 17-22 (2006).
Notice of Allowance corresponding to U.S. Appl. No. 14/304,101 dated Jul. 10, 2017.
Office Action corresponding to U.S. Appl. No. 11/801,609 dated Jun. 14, 2017.
Office Action corresponding to European Patent Application No. 10193414.9 dated May 16, 2017.
Office Action corresponding to U.S. Appl. No. 12/957,947 dated Sep. 19, 2017.
Office Action corresponding to U.S. Appl. No. 13/682,160 dated Dec. 12, 2017.
Office Action (Restriction Requirement) corresponding to U.S. Appl. No. 14/946,169 dated Jan. 4, 2018.
Communication pursuant to Article 94(3) EPC corresponding to European Patent Application Serial No. 12 192 895.6 dated May 12, 2014.
Communication pursuant to Article 94(3) EPC corresponding to European Patent Application Serial No. 12 192 895.6 dated Feb. 18, 2015.
Communication pursuant to Artlcle 94(3) EPC corresponding to European Patent Application Serial No. 12 192 895.6 dated Dec. 9, 2015.
Communication pursuant to Article 94(3) EPC corresponding to European Patent Application Serial No. 12 192 895.6 dated Oct. 7, 2016.
Communication pursuant to Article 94(3) EPC corresponding to European Patent Application Serial No. 12 192 895.6 dated Apr. 13, 2017.
Communication under Rule 71(3) EPC Intention to Grant corresponding to European Patent Application Serial No. 12 192 895.6 dated Apr. 20, 2018.
Extended European Search Report corresponding to European Patent Application No. 12192895.6-1708 dated Mar. 1, 2013.
Office Action corresponding to U.S. Appl. No. 12/322,347 dated Mar. 30, 2018.
Office Action corresponding to U.S. Appl. No. 14/612,175 dated Mar. 30, 2018.
Office Action corresponding to U.S. Appl. No. 12/957,947 dated May 7, 2018.
Office Action corresponding to U.S. Appl. No. 13/682,160 dated Jul. 25, 2018.
Office Action corresponding to U.S. Appl. No. 14/946,169 dated Aug. 16, 2018.
Response to the Summons to Attend Oral Proceedings dated Nov. 15, 2017 corresponding to European Patent Application No. 12192895.6 dated Mar. 27, 2018.
Summons to attend oral proceedings pursuant to Rule 115(1) EPC corresponding to European Patent Application Serial No. 12192895.6 dated Nov. 15, 2017.
Related Publications (1)
Number Date Country
20160236862 A1 Aug 2016 US
Divisions (1)
Number Date Country
Parent 13157876 Jun 2011 US
Child 15042615 US