TRASH BAG WITH MALODOR CONTROL
The trash bag for receiving refuse may include a bag body, the bag body including an inside surface, an outside surface, and a rim defining a mouth with a hem and a draw tape in the hem. The entire bag, the hem area, or the draw tape may contain fragrance, malodor control agents, and fragrance release inhibitors.
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This application claims the benefit of U.S. Provisional Application No. 61/292,347, filed Jan. 5, 2010, which is hereby incorporated by reference in its entirety.
FIELD OF THE INVENTIONThe present invention relates generally to trash bags, and particularly to trash bags with malodor control features, and more particularly to draw tape trash bags with malodor control features.
BACKGROUND OF THE INVENTIONPlastic trash bags have long been used to line trash receptacles. The trash bags encourage sanitary conditions by preventing the refuse from contacting the receptacle. Trash bags also provide a convenient way to remove trash from a receptacle for transport or disposal. Because trash often contains food scraps and other malodor producing items, attempts have been made to produce fragranced trash bags to hide the malodors produced by the bag contents. It is easy to apply volatile fragrance components directly to malodors in the air, for example with the active immediate use of a spray or aerosol air freshening composition. It is much more difficult to control malodors using passive diffusion from plastic trash bags. One of the difficulties is that many fragrance and malodor control agents are not soluble in the typical polyethylene composition of plastic trash bags. Another difficulty is that much of the fragrance and malodor control agents that can be volatilized at ambient temperatures to control malodor formed by trash are substantially volatilized during the trash bag production process, which involves high temperature melt extrusion of polyethylene or other plastics. This volatilization during the production process causes environmental issues within the manufacturing plant, wastes valuable volatile fragrance and odor control agents, and changes the notes of the fragrance and odor control agents as the components are differentially volatilized. These difficulties are particularly apparent in the production of draw tape trash bags, where the bags are large, the production process is complex, and the bags are used in an open configuration.
BRIEF SUMMARY OF THE INVENTIONIn one embodiment, the bag may further comprise a front wall, a back wall, and a hem, the hem defining the rim. The hem may further define a passageway, which is at least partially enclosed. The hem may include a first opening and a second opening. The bag may comprise a draw tape, which is disposed within the passageway. The draw tape may be accessible via the first and second openings in the hem. The hem, the hem passageway, and the draw tape may comprise a hem area. The hem may include a fragrance, a malodor control agent and a fragrance release inhibitor. If the first and second hem openings are small relative to the total hem area, then any fragrance released in the interior of the hem may be trapped and effectively build up in concentration within the hem interior. This may also be the case if the film layer on the hem exterior has a composition such that it is a barrier to fragrance transmission.
In another embodiment, the bag may comprise a bag body including a first portion. The first portion may include an upper rim, which defines a mouth. The bag may further comprise a second portion disposed below the first portion, the second portion defining a closed bottom to the bag. The bag body may be thicker in the first portion than in the second portion.
In another embodiment, the bag may comprise a bag body, the bag body having an inside surface and an outside surface. The bag may comprise a rim, which defines a mouth. The bag may further comprise a hem that defines the rim. The hem area may define a passageway, the passageway being at least partially enclosed. The hem area may further include an inside surface, an outside surface, a first opening, and a second opening. The bag may also comprise a draw tape disposed within the passageway. The draw tape may be accessible via the first and second openings in the hem. The draw tape may contain a fragrance, a malodor control agent, and a fragrance release inhibitor.
When the hem has a length shorter than the length of the bottom of the bag, the hem may fit snugly at the top of the trash can or may limit the volume of air circulating into and out of the trash bag and effectively control malodors inside the bag from being offensive at the bag opening. When the hem is patterned, the interior of the hem may contain restricted areas for the build-up of fragrance concentration. This may also help to effectively control malodors inside the bag from being offensive at the bag opening.
In another embodiment, the bag may comprise a bag body having an inside surface and an outside surface. The bag may comprise an undulating rim, the rim defining a mouth. The rim may include at least two flaps, wherein the flaps may be tied together to at least partially close the bag.
These films can be made by a conventional flat or tubular cast extrusion or coextrusion, or other suitable process such as a blown film process to produce monolayer, bilayer, trilayer or multilayer films. If desired for a given end use, these films can be oriented by tenterframe, or other suitable process. They can thereafter optionally be annealed. The films of the present invention are typically produced by the blown film or cast film process. The blown or cast film is formed by extrusion. For the blown film process, the film can be collapsed to double the plies of the film or the film can be cut and folded or cut and unfolded. The extruder is a conventional one using a die, which will provide the desired gauge. Some useful extruders are described in U.S. Pat. Nos. 4,814,135; 4,857,600; 5,076,988; 5,153,382; each of which are incorporated herein by reference. The gauge of the films of interest here can be in the range of about 0.1 to about 10 mils, suitably from about 0.2 to about 4 mils, and suitably in the range of about 0.3 to about 2 mils. Examples of various extruders, which can be used in producing the film of the present invention, are the single screw type modified with a blown film die and air ring and continuous take off equipment.
Using a blown film extrusion or co-extrusion process, the fragrance, malodor control agents, or combination can be either dispersed in equivalent concentration throughout the bag or can be concentrated in one area of the bag or in one or more layers of the bag. A suitable method of concentrating the fragrance or malodor control agents within a specific area of the bag can involve localized delivery of the fragrance, malodor control agent, or the combination to one area of one or more layers of the film through individual extruders and the same die or by producing a thicker film in one area of the die or one of the film layers. In the blown film extrusion or co-extrusion process, the film is typically slit to form a flat film which becomes the bag. If the film is slit consistently in the area of film adjacent to higher concentrations of fragrance, malodor control agent, or the combination, then there would be higher concentrations of fragrance, malodor control agent, or the combination near the top of the bag, and in the hem area, if the hem area was formed from the top of the bag. The hem, the hem passageway, and the draw tape may comprise a hem area. If the film is slit consistently in the area of film opposite to higher concentrations of fragrance, malodor control agent, or the combination, then there would be higher concentrations of fragrance, malodor control agent, or the combination near the bottom of the bag. Using blown film co-extrusion, the fragrance, malodor control agent, or the combination could also be localized by layer. For example, the fragrance, malodor control agent, or the combination could be in the outside layer, the inner layer, or one or more of the core layers, as described below. Additionally, a hem may be attached to the bag after extrusion of the bag film, which would allow the fragrance, malodor control agent, or the combination to be concentrated in the hem area.
The film materials may be any thermoplastic material, typically LLDPE (linear low density polyethylene), and the film compositions may differ slightly according to their use or where there is a multilayer film, the film layers may differ from each other. For example, the film layers may have different strength or barrier properties, or properties designed for better sealing. The fragrance, malodor control agent, or the combination may be concentrated in a core layer or may be entirely within a core layer. The core layer, or other layers, for example two or more exterior layers may also contain reclaimed thermoplastic material and a fragrance release inhibitor, such as titanium dioxide. Additional fragrance release inhibitors include starch, clays and nanoclays, talc, and microcapsules.
An example of a bilayer film 10 is shown in
Fragrance is typically introduced as thermoplastic pellets, the fragrance master batch, suitably containing 5 to 50% fragrance, or 10 to 40% fragrance, or 20-30% fragrance. This fragrance master batch can also contain 1 to 40%, or 5 to 30%, or 10 to 20% of malodor control agents. The fragrance master batch is mixed in the extruder with other thermoplastic pellets, of different or similar material, either virgin plastic or recycled or reclaimed plastic, and optionally a fragrance release inhibitor, such as titanium dioxide. In addition, other additives may be included. The final concentration of the fragrance in the film may be 0.01 to 0.5%, or 0.02 to 0.4, or 0.05 to 0.3%, or 0.1 to 0.2%. The final concentration of the malodor control agent in the film may be 0.01 to 0.5%, or 0.02 to 0.4, or 0.05 to 0.3%, or 0.1 to 0.2%. The final concentration of the fragrance release inhibitor in the film may be 0.5 to 10%, or 1 to 8% or 2 to 6%. The final concentration of the fragrance in a layer of a multilayer film may be 0.01 to 0.5%, or 0.02 to 0.4, or 0.05 to 0.3%, or 0.1 to 0.2%. The final concentration of the malodor control agent in a layer of a multilayer the film may be 0.01 to 0.5%, or 0.02 to 0.4, or 0.05 to 0.3%, or 0.1 to 0.2%. The final concentration of the fragrance release inhibitor in a layer of a multilayer the film may be 0.5 to 10%, or 1 to 8% or 2 to 6%. The fragrance containing film layer may be a core layer or an outside layer. Where the fragrance containing film layer is a core layer, the core layer or layers may comprising 20 to 90%, or 40 to 80%, or 50 to 60% of the multilayer film.
A draw tape bag includes of two layers of plastic film which are sealed on three sides and open on the remaining side to form an opening in the bag. A hem securing the draw tape is provided at the periphery of the open end whereby the tape is accessed through openings in the hem. By pulling the draw tape, the opening in the bag closes. Consequently, the draw tape serves as a handle whereby the bag may be grasped to be subsequently transported. The hem in a draw tape bag is formed by two layers of film which are fused together to create a hem seal. The hem seal is typically created by heating the film until it melts and then fusing the two layers together. Heat sealing operations typically create a strong bond which cannot be separated without destroying the film, otherwise known as a destructive bond. Draw tape bags and methods for making draw tape bags are shown in U.S. Pat. Nos. 4,867,735, 4,966,059, and 5,006,380 which are incorporated herein by reference. In one embodiment, the draw tape may include a single layer. In one embodiment, the draw tape may include a first exterior layer, a second exterior layer, and at least one core layer disposed between the exterior layers as described in PCT App. WO2008156952 to O'Donnell et al. The draw tape may contain a fragrance, a malodor control agent, and a fragrance release inhibitor in either an exterior layer or a core layer.
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The hem 1334 may have increased thickness to improve the strength of the bag at the hem 1334, an area where the bag 1330 may experience increased stresses due to the user holding the bag 1330 at the rim 1336 or by the draw tape 1348. In other suitable embodiments, the hem 1334 may be patterned 1360.
Referring to
In a suitable embodiment in
Bags may be produced in a high speed, automated manufacturing process such as the one illustrated in
To provide the interior volume of the finished bag, the web 1701 may be folded in half orthogonally about the machine direction 1706 by a folding operation 1718 so that the web is arranged as first and second opposing, adjacent webs halves 1720, 1722 being advanced in parallel along the machine direction 1706. When folded in half, the first and second side edges 1710, 1712 are moved adjacent to each other. The width 1716 of the folded web 1701 may be half of the width 1714 of the unfolded web. Moreover, once folded, the center of the web 1701 provides a crease 1724 that may correspond to the bottom edge of the finished bag. In another embodiment, the roll 1702 may include a pre-folded web and the folding operation is not necessary. In another embodiment, a first web from a first roll and a second web from a second roll may be provided and advanced in parallel along the machine direction. The first and second webs may be joined along one edge to form the bottom portion of the bags.
In the embodiments, where a pattern may be imparted proximate to the top of the bag, the process may include one or more rollers 1726 to impart the pattern to the bag.
The hems may be formed along the adjacent edges 1710, 1712 by a hem forming operation 1730 in which hem flaps may be tucked or folded into the web 1701. A hem may be formed for each of the adjacent edges 1710, 1712. The hemming operation may add notches 1732. The notches 1732 may be of any suitable shape or size and may be made through the advancing web 1701 intermittently along the adjacent edge 1710, 1712.
To provide the draw tape, a continuous strip 1740 of thermoplastic thin-film material may be unwound from a roll 1742 of such material. The strip 1740 is directed by various rollers and/or nips toward the advancing web where it may be inserted into the hems.
The manufacturing process 1700 may include equipment to pre-stretch the strip 1740 prior to installation in the bag. For example, the processing equipment may include a pair of opposing cylindrical rollers 1743 that are located before and spaced from a pair of rollers 1744. The strip material 1740 may be directed between the pair of rollers 1743 and then onto the pair of opposing cylindrical rollers 1744. If the pair of rollers 1744 are rotated at a faster relative speed than the pair of rollers 1743, the differential roller speeds will place the thermoplastic strip under tension and may thereby stretch or elongate it. This process of stretching may be referred to as pre-stretching. In a further embodiment, the relative speed of the pairs of rollers 1743, 1744 may be adjusted to vary the amount and location of the pre-stretching induced onto the strip 1740. For example, where the relative speed of the rollers is equal, the tape will undergo little or no stretching. If the differential speed is increased, the tape will be stretched and possibly neck down in width. Thus, varying the relative speed of the roller pairs with respect to each other may produce draw tapes with sections that may be pre-stretched and sections that may not be pre-stretched, the pre-stretched sections may be narrower than the sections that are not pre-stretched.
Referring to
To keep the strip 1740 including the pattern 1748 in a predetermined stretched or expanded condition, a second pair of opposing rollers 1749 may be provided downward from the patterning rollers 1745 and may be rotated at a speed necessary to maintain the predetermined stretched condition.
The stretched strip 1740 may then be directed toward the adjacent edges 1710, 1712 of the advancing web 1701 where the strip 1740 may be inserted in the hemming operation 1730. Once inserted, the strip 1740 is accessible through the notches 1732. A second roll of strip material may be similarly provided for insertion into the remaining hem of the two adjacent edges. It should be appreciated that in other embodiments of the manufacturing process, the order and/or presence of the hemming, notching and strip insertion operations may be altered or changed.
In another embodiment, the strip 1740 may not be stretched by rollers 1743, 1744, but may be processed by the rollers 1745 to receive the pattern. The strip 1740 may then be inserted under tension in the hem. The tension may or may not be sufficient to stretch or expand the pattern.
In another embodiment, rollers similar to rollers 1726 may be used, after the hem forming operation, in order to impart a pattern to the hem and draw tape, and/or the bag side wall while the draw tape is in the hem, such as, the rollers 2226 in
The web 1701 and strip 1740 may be directed through various other processing steps to produce the finished bag. For example, the web 1701 may be directed through a heat sealing operation 1750 in which heat seals 1752 are formed at intermittent spaces along the web between the adjacent edges 1710, 1712 and the folded crease 1724 so as to be perpendicular to the machine direction 1706. The heat sealing operation 1750 may melt together and thereby attach the two folded web halves and the strip 1740 within the region of the heat seal 1752. The heat seals 1752 may be performed while the strip 1740 is in the stretched state. The web 1701 may be directed through a perforating operation 1754 in which perforations 1758 are made between or into the heat seals 1752 between the adjacent edges 1710, 1712 and the crease 1724. The perforation may be disposed through both the folded web and strip 1740. As may be appreciated, the heat seals 1752 and perforations 1758 may correspond to the side edges of the finished bags 1760. To prevent the strip 1740 from unintentionally recovering and distorting the web 1701 advancing through the processing machinery, the web may be kept under tension along the machine direction 1706. In another embodiment, the web may be folded one or more times before the folded web may be directed through the perforating operation. The web 1701 embodying the finished bags 1760 may be wound into a roll 1762 for packaging and distribution.
In another embodiment of the process which is illustrated in
Referring another embodiment in
The hems may be formed along the adjacent edges 2210, 2212 by a hem forming operation 2230 in which hem flaps may be tucked and folded into the web 2201. A hem may be formed for each of the adjacent edges 2210, 2212. The hem forming operation may add notches 2232.
To provide the draw tape, a continuous strip 2240 of thermoplastic thin-film material may be unwound from a roll 2242 of such material. The strip 2240 is directed by various rollers and/or nips toward the advancing web where it may be inserted into the hems.
Referring to
The strip 2240 may be in a relaxed state when the strip is inserted into the hem. A second roll of strip material may be similarly provided for insertion into the remaining hem of the two adjacent edges. It should be appreciated that in other embodiments of the manufacturing process, the order and/or presence of the hemming, notching and strip insertion operations may be altered or changed.
In another embodiment, the strip 2240 may not be stretched by rollers 2243, 2244, but may be processed by the rollers 2245 to receive the pattern 2248. The strip 2240 may be in a relaxed state when the strip is inserted into the hem.
Rollers 2226 may be used, after the hemming operation, in order to impart a pattern to the hem and draw tape, and/or the bag side wall while the draw tape is in the hem. These rollers may be used at any location after the hemming operation and before the web is separated into bags or rolled for consumer use. In another embodiment, the rollers 2245 with the pattern may not be necessary because the rollers 2226 may impart the pattern to the hem and strip at the same time.
The web 2201 and strip 2240 may be directed through various other processing steps to produce the finished bag. For example, the web 2201 may be directed through a heat sealing operation 2250 in which heat seals 2252 are formed at intermittent spaces along the web. The process may include the application of the inward seals during the sealing operation 2250, or at another location in the process, as appropriate.
The heat seals 2252 may be performed while the strip 2240 is in the relaxed state. The web 2201 may be directed through a perforating operation 2254 in which perforations 2258 are made between or into the heat seals 2252. The perforation may be disposed through both the folded web and strip 2240. As may be appreciated, the heat seals 2252 and perforations 2258 may correspond to the side edges of the finished bags 2260. In another embodiment, the web may be folded one or more times before the folded web may be directed through the perforating operation. The web 2201 embodying the finished bags 2260 may be wound into a roll 2262 for packaging and distribution.
The films of the invention can typically undergo one or more film stretching processes. During these stretching processes, the film thickness may be significantly decreased. Therefore referring again to
A second method of stretching is called tentering. In simplest terms, the tentering method involves grabbing the sides of the film and stretching it sideways. For many years this was the only way to stretch film from side to side, or in the transverse direction (TD). The tentering method tended to be slow and, because the forces are concentrated on the edges of the film, often the film did not stretch evenly. U.S. Pat. No. 4,704,238 discloses a tentering apparatus having a pre-heating zone and a stretching zone, followed by a heat setting zone to facilitate the stretching of a preformed blown or cast film.
A third method of stretching involves incremental stretching of thermoplastic film. This method is described in the early patent literature, for example, U.S. Pat. Nos. 4,153,751; 4,116,892; 4,289,832 and 4,438,167. In the practice of this method, the film is run between grooved or toothed rollers. The grooves or teeth on the rollers intermesh without touching when the rollers are brought together and, as the film passes between the rollers, it is stretched. Incremental stretching has the advantage of causing the film to stretch in many small increments that are evenly spaced over the entire film. This results in a more evenly stretched film, something that is not always true for MDO stretching and is almost never true for tentering. Incremental stretching allows one to stretch the film in the MD, TD and at angle (DD or diagonal direction) or any combination of these three directions. The depth at which the intermeshing teeth engage controls the degree of stretching. Often, this incremental method of stretching is simply referred to as TD, MD, TD/MD or DD ring rolling. A number of U.S. patents have issued for incrementally stretching thermoplastic films and laminates. An early example of the patent art which discloses a method of incrementally stretching film is U.S. Pat. No. 5,296,184. Other relevant patents regarding the incremental stretching of thermoplastic films and laminates include U.S. Pats. Nos. 6,265,045; 6,214,147; 6,013,151; 5,865,926; 5,861,074; 5,851,937; 5,422,172 and 5,382,461.
The diagonal intermeshing stretcher consists of a pair of left hand and right hand helical gear-like elements on parallel shafts. The shafts are disposed between two machine side plates, the lower shaft being located in fixed bearings and the upper shaft being located in bearings in vertically slidable members. The slidable members are adjustable in the vertical direction by wedge shaped elements operable by adjusting screws. Screwing the wedges out or in will move the vertically slidable member respectively down or up to further engage or disengage the gear-like teeth of the upper intermeshing roll with the lower intermeshing roll. Micrometers mounted to the side frames are operable to indicate the depth of engagement of the teeth of the intermeshing roll.
The intermeshing rolls closely resemble fine pitch helical gears. In the preferred embodiment, the rolls have 5.935″ diameter, 45° helix angle, a 0.100″ normal pitch, 30 diametral pitch, 14½° pressure angle, and are basically a long addendum topped gear. This produces a narrow, deep tooth profile which allows up to about 0.090″ of intermeshing engagement and about 0.005″ clearance on the sides of the tooth for material thickness. The teeth are not designed to transmit rotational torque and do not contact metal-to-metal in normal intermeshing stretching operation.
The TD intermeshing stretching equipment is identical to the diagonal intermeshing stretcher with differences in the design of the intermeshing rolls and other minor areas noted below. Since the TD intermeshing elements are capable of large engagement depths, it is important that the equipment incorporate a means of causing the shafts of the two intermeshing rolls to remain parallel when the top shaft is raising or lowering. This is necessary to assure that the teeth of one intermeshing roll always fall between the teeth of the other intermeshing roll and potentially damaging physical contact between intermeshing teeth is avoided. This parallel motion is assured by a rack and gear arrangement wherein a stationary gear rack is attached to each side frame in juxtaposition to the vertically slidable members. A shaft traverses the side frames and operates in a bearing in each of the vertically slidable members. A gear resides on each end of this shaft and operates in engagement with the racks to produce the desired parallel motion.
The drive for the TD intermeshing stretcher must operate both upper and lower intermeshing rolls except in the case of intermeshing stretching of materials with a relatively high coefficient of friction. The drive need not be antibacklash, however, because a small amount of machine direction misalignment or drive slippage will cause no problem. The reason for this will become evident with a description of the TD intermeshing elements.
The TD intermeshing elements are machined from solid material but can best be described as an alternating stack of two different diameter disks. In the preferred embodiment, the intermeshing disks would be 6″ in diameter, 0.031″ thick, and have a full radius on their edge. The spacer disks separating the intermeshing disks would be 5½″ in diameter and 0.069″ in thickness. Two rolls of this configuration would be able to be intermeshed up to 0.231″ leaving 0.019″ clearance for material on all sides. As with the diagonal intermeshing stretcher, this CD intermeshing element configuration would have a 0.100″ pitch.
The MD intermeshing stretching equipment is identical to the diagonal intermeshing stretch except for the design of the intermeshing rolls. The MD intermeshing rolls closely resemble fine pitch spur gears. In the preferred embodiment, the rolls have a 5.933″ diameter, 0.100″ pitch, 30 diametral pitch, 14½° pressure angle, and are basically a long addendum, topped gear. A second pass was taken on these rolls with the gear hob offset 0.010″ to provide a narrowed tooth with more clearance. With about 0.090″ of engagement, this configuration will have about 0.010″ clearance on the sides for material thickness.
The film may additionally be embossed with a pattern that provides texture to the film, but with no additional overall stretching. The film may be embossed by feeding between two rolls, one or both of which have an embossing pattern. The rolls may be heated or unheated. In one embodiment in
Laminating two or more film layers together may allow coating of actives on the surface of a film that can then be laminated to another film to result in the actives being concentrated on the interior of the laminate, as shown in the process in
To impart or form the lamination of the films 2001, 2002, the processing equipment may include a cylindrical roller 2030 and an adjacent second cylindrical roller 2032 between which the films 2001, 2002 may be directed by the processing equipment. The rollers 2030, 2032 may be arranged so that their longitudinal axes may be perpendicular to the machine direction 2006 and may be adapted to rotate about their longitudinal axes in opposite rotational directions. In various embodiments, motors may be provided that power rotation of the rollers 2030, 2032 in a controlled manner. The first and second rollers 2030, 2032 may be made from any suitable material including, for example, metal, such as, steel or titanium. The rollers 2030, 2032 may have discontinuous ridges on the rollers which may impart the discontinuous patterns into the film layers during the process of discontinuous lamination. After the film layers 2001, 1202 have passed between the rollers 2030, 2032, the laminate film 2050 includes discontinuous patterns 2076 of bonded areas with unbonded areas 2078 in between.
To provide the two opposing sidewalls of the finished bag, the film laminate 2050 may be folded by a folding operation 2020. During the folding operation 2020, the first edge 2010 of the laminate 2050 is moved adjacent to the second edge 2012 so as to form a fold edge 2026 that may run parallel with the machine direction 2006. The folded laminate 2052 may have a width 2028 that is half of the original width 2008. The processing equipment may further process the folded laminate 2052 after it passes through the folding operation 2020. For example, referring to
The film may be coated or printed with an ink, adhesive, or other functional compound, such as a fragrance to film layer 2002 by process 2022 before lamination in rollers 2030, 2032. Depending upon the composition, various coating and printing process may be appropriate for process 2022. For instance, in addition to ink jet printing and other non-impact printers, the composition can be used in screen printing processes, offset lithographic processes, flexographic printing processes, rotogravure printing processes, and the like. In other cases, a coating process may be appropriate. In the gravure coating process, an engraved roller runs in coating bath which fills the engraved recesses in engraved roller with excess additive delivery slurry. The excess slurry on engraved roller is wiped off engraved roller by doctor blade, with engraved roller thereafter depositing additive delivery slurry layer onto substrate film as substrate film passes between engraved roller and pressure roller. In the 3-roll reverse roll coating process, additive delivery slurry is measured onto application roller by gap between upper metering roller and application roller. The coating is “wiped off” application roller by substrate film as substrate passes around support roller, leaving a desired layer of slurry on substrate. Additive delivery slurry is confined on metering roller by doctor blade. In the Meyer rod coating process, an excess coating of the additive delivery slurry is deposited onto substrate film as substrate film passes over bath roller, which is immersed in bath containing the additive delivery slurry. Wire-wound Meyer rod allows a desired quantity of the coating to remain on substrate film. The quantity of coating remaining is determined by the diameter of the wire used on Meyer rod, as well as the distance of the surface of the wire from the substrate film. Although the wire can be in contact with substrate film, alternatively the wire can be spaced from substrate film by, for example, 1 to 10 mils, or 2 to 6 mils. In the extrusion coating process, additive delivery slurry is extruded through slot, forming coating on substrate. In the curtain coating process, a bath containing additive delivery slurry has slot in its base, allowing continuous curtain of additive delivery slurry to fall towards gap between conveyors. Substrate is passed along the conveyors at a controlled speed, receiving coating thereon. In the air knife coating process, excess coating is applied to substrate, with the excess coating being reduced to a desired coating by the gas flow emanating from blower. In the rotary screen printing process, a squeegee presses additive delivery slurry through holes in rotary screen. Substrate is passed through a nip between rotary screen and counter pressure roller, resulting in printed substrate.
Many of the above earlier embodiments may be combined with each other to create further embodiments of the bag. Accordingly, all of the features discussed in the earlier described embodiments may be included in any of the other embodiments disclosed herein, as appropriate.
The bag and bag components may be made of thermoplastic. The materials are suitably hydrophobic polymers not derivatized by actives, such as fragrance components and malodor control agents. Useful materials in the inventive films include but are not limited to thermoplastic polyolefins, including polyethylene and copolymers thereof and polypropylene and copolymers thereof. Suitable polyethylenes include high density polyethylene, medium density polyethylene, low density polyethylene, very low density polyethylene, and linear low density polyethylene.
The olefin based polymers include the most common ethylene or propylene based polymers such as polyethylene, polypropylene, and copolymers such as ethylene vinylacetate (EVA), ethylene methyl acrylate (EMA) and ethylene acrylic acid (EAA), or blends of such polyolefins. Other examples of polymers suitable for use as films include elastomeric polymers. Suitable elastomeric polymers may also be biodegradable or environmentally degradable. Suitable elastomeric polymers for the film include poly(ethylene-butene), poly(ethylene-hexene), poly(ethylene-octene), poly(ethylene-propylene), poly(styrene-butadiene-styrene), poly(styrene-isoprene-styrene), poly(styrene-ethylene-butylene-styrene), poly(ester-ether), poly(ether-amide), poly(ethylene-vinylacetate), poly(ethylene-methylacrylate), poly(ethylene-acrylic acid), poly(ethylene butylacrylate), polyurethane, poly(ethylene-propylene-diene), ethylene-propylene rubber. This new class of rubber-like polymers may also be employed and they are generally referred to herein as metallocene polymers or polyolefins produced from single-cite catalysts. The most preferred catalysts are known in the art as metallocene catalysts whereby ethylene, propylene, styrene and other olefins may be polymerized with butene, hexene, octene, etc., to provide elastomers suitable for use in accordance with the principles of this invention, such as poly(ethylene-butene), poly(ethylene-hexene), poly(ethylene-octene), poly(ethylene-propylene), and/or polyolefin terpolymers thereof. It can be suitable to blend into the resin a suitable amount of a cling agent, such as polyisobutylene, to control the level of lamination during the lamination process.
Fragrance technology is intended to include fragrancing compounds and compositions as well as malodor control agents and compositions (regardless of whether these malodor control agents themselves are fragrances). Fragrance technology compositions can be chosen so as to have relatively low solubility in water and be hydrophobic. They should be chosen so as to maximize those with low levels of solubility and minimize low levels of those which are relatively soluble or immiscible in water. Suitably, the fragrance technology compositions also have a low rate of evaporation.
For covering malodors, grapefruit fragrance character was found to be more suitable than lemon citrus fragrance character. Especially suitable is grapefruit fragrance which may contain Limonene, Geraniol, Citral, Citronellal, or Neral. The grapefruit fragrance can also contain 1,1-Dimethoxy-2,2,5-trimethylhex-4-ene, N-methyl-N-phenyl-2-methylbutanamide, 1-p-methene-8-thiol, thiobenzoic acids, 2,4,6-trimethyl-4-phenyl-1,3-dioxane, 2,6-dimethyl-6-(3-methyl-but-2-enyl)-cyclo-hex-2-enone, 2,4,6-trimethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enone, 2,2,6-trimethyl-6-(3-methyl-but-2-enyl)-cyclohex-3-enone, 2,6-Dimethyl-2-(3-methyl-but-2-enyl)-cyclohexanone, 1,2,6-trimethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enol, 6-methoxy-1,5,6-trimethyl-5-(3-methyl-but-2-enyl)-cyclohexene, 1,2,4,6-Tetramethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enol, 2,6-Dimethyl-6-(3-methyl-but-2-enyl)-1-vinyl-cyclohex-2-enol, 2,6-Dimethyl-1-ethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enol, 2,6-dimethyl-6-(3-methyl-but-2-enyl)-cyclo-hex-2-enol, 1,2,6-Trimethyl-6-(3-methyl-but-2-enyl)-cyclohexa-2,4-dienol, and 2-(2,3-Dimethyl-but-2-enyl)-2,6-dimethyl-cyclohexanone
For covering malodors, a synthetic vanilla fragrance character was found to be more suitable than natural vanilla fragrance character. The vanilla fragrance can contain acetanisole, anisyl acetate, anisyl alcohol, anisyl propionate, benzoin, cinnamaldehyde, ethyl vanillin, 2-methoxy-4-methylphenol, 1-(p-methoxyphenyl)-2-propanone, propenyl guaethol, veratraldehyde, vanillylacetone, vanillin isobutyrate, veratrole, and acetovanillone compounds.
Fragrances and fragrance oils comprise perfume raw materials (“PRMs”) as well as other less volatile materials. PRMs are characterized by their boiling point (B.P.) and their octanol/water partitioning coefficient (P). The boiling points of many fragrance ingredients are reported in, e.g., “Perfume and Flavor Chemicals (Aroma Chemicals),” Steffen Arctander, published by the author, 1969. The octanol/water partitioning coefficient of a material is the ratio between its equilibrium concentrations in octanol and in water. The octanol/water partitioning coefficient can alternatively be reported on a base 10 logarithmic scale, as logP, and when the calculated value is reported, as ClogP. The logP of many perfume ingredients has been reported; for example, the Pomona92 database, available from Daylight Chemical Information Systems, Inc. (Daylight CIS), Irvine, Calif., contains many, along with citations to the original literature. However, the logP values are most conveniently calculated by the “CLOGP” program, also available from Daylight CIS. This program also lists experimental logP values when they are available in the Pomona92 database. The “calculated logP” (ClogP) is determined by the fragment approach of Hansch and Leo (cf., A. Leo, in Comprehensive Medicinal Chemistry, Vol. 4, C. Hansch, P. G. Sammens, J. B. Taylor and C. A. Ramsden, Eds., p. 295, Pergamon Press, 1990). The fragment approach is based on the chemical structure of each perfume ingredient, and takes into account the numbers and types of atoms, the atom connectivity, and chemical bonding. The ClogP values, which are the most reliable and widely used estimates for this physicochemical property, are preferably used instead of the experimental logP values in the selection of perfume ingredients which are useful in the present invention.
Suitably, at least 30%, or at least 40%, or at least 50% of the perfume ingredients for use in this invention typically have ClogP of greater than 3.5. Suitably, at least 30%, or at least 40%, or at least 50% of the perfume ingredients for use in this invention have a boiling point greater than 250° C. Below in Table 1 are listed typical suitable fragrance ingredients.
Suitable fragrance ingredients include extracts from natural raw materials such as essential oils, concretes, absolutes, resins, resinoids, balsams, tinctures such as for example ambergris tincture; amyris oil; angelica seed oil; angelica root oil; aniseed oil; valerian oil; basil oil; tree moss absolute; bay oil; armoise oil; benzoe resinoid; bergamot oil; beeswax absolute; birch tar oil; bitter almond oil; savory oil; buchu leaf oil; cabreuva oil; cade oil; calamus oil; camphor oil; cananga oil; cardamom oil; cascarilla oil; cassia oil; cassie absolute; castoreum absolute; cedar leaf oil; cedar wood oil; cistus oil; citronella oil; lemon oil; copaiba balsam; copaiba balsam oil; coriander oil; costus root oil; cumin oil; cypress oil; davana oil; dill weed oil; dill seed oil; eau de brouts absolute; oakmoss absolute; elemi oil; estragon oil; eucalyptus citriodora oil; eucalyptus oil (cineole type); fennel oil; fir needle oil; galbanum oil; galbanum resin; geranium oil; grapefruit oil; guaiacwood oil; gurjun balsam; gurjun balsam oil; helichrysum absolute; helichrysum oil; ginger oil; iris root absolute; iris root oil; jasmine absolute; calamus oil; blue camomile oil; Roman camomile oil; carrot seed oil; cascarilla oil; pine needle oil; spearmint oil; caraway oil; labdanum oil; labdanum absolute; labdanum resin; lavandin absolute; lavandin oil; lavender absolute; lavender oil; lemon-grass oil; lovage oil; lime oil distilled; lime oil expressed; linaloe oil; Litsea cubeba oil; laurel leaf oil; mace oil; marjoram oil; mandarin oil; massoi (bark) oil; mimosa absolute; ambrette seed oil; musk tincture; clary sage oil; nutmeg oil; myrrh absolute; myrrh oil; myrtle oil; clove leaf oil; clove bud oil; neroli oil; olibanum absolute; olibanum oil; opopanax oil; orange flower absolute; orange oil; origanum oil; palmarosa oil; patchouli oil; perilla oil; Peru balsam oil; parsley leaf oil; parsley seed oil; petitgrain oil; peppermint oil; pepper oil; pimento oil; pine oil; pennyroyal oil; rose absolute; rosewood oil; rose oil; rosemary oil; Dalmatian sage oil; Spanish sage oil; sandalwood oil; celery seed oil: spike-lavender oil; star anise oil; storax oil; tagetes oil; fir needle oil; tea tree oil; turpentine oil; thyme oil; Tolu balsam; tonka bean absolute; tuberose absolute; vanilla extract; violet leaf absolute; verbena oil; vetiver oil; juniperberry oil; wine lees oil; wormwood oil; wintergreen oil; ylang-ylang oil; hyssop oil; civet absolute; cinnamon leaf oil; cinnamon bark oil; and fractions thereof or ingredients isolated therefrom; individual fragrance ingredients from the group comprising hydrocarbons, such as for example 3-carene; α-pinene; β-pinene; α-terpinene; γ-terpinene; p-cymene; bisabolene; camphene; caryophyllene; cedrene; farnesene; limonene; longifolene; myrcene; ocimene; valencene; (E,Z)-1,3,5-undecatriene; styrene; diphenylmethane; aliphatic alcohols, such as for example hexanol; octanol; 3-octanol; 2,6-dimethyl-heptanol; 2-methyl-2-heptanol, 2-methyl-2-octanol; (E)-2-hexenol; (E)- and (Z)-3-hexenol; 1-octen-3-ol; a mixture of 3,4,5,6,6-pentamethyl-3/4-hepten-2-ol and 3,5,6,6-tetramethyl-4-methyleneheptan-2-ol; (E,Z)-2,6-nonadienol; 3,7-dimethyl-7-methoxyoctan-2-ol; 9-decenol; 10-undecenol; 4-methyl-3-decen-5-ol; aliphatic aldehydes and their acetals such as for example hexanal; heptanal; octanal; nonanal; decanal; undecanal; dodecanal; tridecanal; 2-methyloctanal; 2-methylnonanal; (E)-2-hexenal; (Z)-4-heptenal; 2,6-dimethyl-5-heptenal; 10-undecenal; (E)-4-decenal; 2-dodecenal; 2,6,10-trimethyl-5,9-undecadienal; heptanal-diethylacetal; 1,1-dimethoxy-2,2,5-trimethyl-4-hexene; citronellyl oxyacetaldehyde; aliphatic ketones and oximes thereof, such as for example 2-heptanone; 2-octanone; 3-octanone; 2-nonanone; 5-methyl-3-heptanone; 5-methyl-3-heptanone oxime; 2,4,4,7-tetramethyl-6-octen-3-one; aliphatic sulfur-containing compounds, such as for example 3-methylthiohexanol; 3-methylthiohexyl acetate; 3-mercaptohexanol; 3-mercaptohexyl acetate; 3-mercaptohexyl butyrate; 3-acetyltbiohexyl acetate; 1-menthene-8-thiol; aliphatic nitriles, such as for example 2-nonenenitrile; 2-tridecenenitrile; 2,12-tridecenenitrile; 3,7-dimethyl-2,6-octadienenitrile; 3,7-dimethyl-6-octenenitrile; aliphatic carboxylic acids and esters thereof, such as for example (E)- and (Z)-3-hexenylformate; ethyl acetoacetate; isoamyl acetate; hexyl acetate; 3,5,5-trimethylhexyl acetate; 3-methyl-2-butenyl acetate; (E)-2-hexenyl acetate; (E)- and (Z)-3-hexenyl acetate; octyl acetate; 3-octyl acetate; 1-octen-3-yl acetate; ethyl butyrate; butyl butyrate; isoamyl butyrate; hexylbutyrate; (E)- and (Z)-3-hexenyl isobutyrate; hexyl crotonate; ethylisovalerate; ethyl-2-methyl pentanoate; ethyl hexanoate; allyl hexanoate; ethyl heptanoate; allyl heptanoate; ethyl octanoate; ethyl-(E,Z)-2,4-decadienoate; methyl-2-octinate; methyl-2-noninate; allyl-2-isoamyl oxyacetate; methyl-3,7-dimethyl-2,6-octadienoate; acyclic terpene alcohols, such as, for example, citronellol; geraniol; nerol; linalool; lavandulol; nerolidol; farnesol; tetrahydrolinalool; tetrahydrogeraniol; 2,6-dimethyl-7-octen-2-ol; 2,6-dimethyloctan-2-ol; 2-methyl-6-methylene-7-octen-2-ol; 2,6-dimethyl-5,7-octadien-2-ol; 2,6-dimethyl-3,5-octadien-2-ol; 3,7-dimethyl-4,6-octadien-3-ol; 3,7-dimethyl-1,5,7-octatrien-3-ol 2,6-dimethyl-2,5,7-octatrien-1-ol; as well as formates, acetates, propionates, isobutyrates, butyrates, isovalerates, pentanoates, hexanoates, crotonates, tiglinates and 3-methyl-2-butenoates thereof; acyclic terpene aldehydes and ketones, such as, for example, geranial; neral; citronellal; 7-hydroxy-3,7-dimethyloctanal; 7-methoxy-3,7-dimethyloctanal; 2,6,10-trimethyl-9-undecenal; α-sinensal; β-sinensal; geranylacetone; as well as the dimethyl- and diethylacetals of geranial, neral and 7-hydroxy-3,7-dimethyloctanal; cyclic terpene alcohols, such as, for example, menthol; isopulegol; alpha-terpineol; terpinen-4-ol; menthan-8-ol; menthan-1-ol; menthan-7-ol; borneol; isoborneol; linalool oxide; nopol; cedrol; ambrinol; vetiverol; guaiol; and the formates, acetates, propionates, isobutyrates, butyrates, isovalerates, pentanoates, hexanoates, crotonates, tiglinates and 3-methyl-2-butenoates of alpha-terpineol; terpinen-4-ol; methan-8-ol; methan-1-ol; methan-7-ol; borneol; isoborneol; linalool oxide; nopol; cedrol; ambrinol; vetiverol; guaiol; cyclic terpene aldehydes and ketones, such as, for example, menthone; isomenthone; 8-mercaptomenthan-3-one; carvone; camphor; fenchone; alpha-ionone; beta-ionone; alpha-n-methylionone; beta-n-methylionone; alpha-isomethylionone; beta-isomethylionone; alpha-irone; alpha-damascone; beta-damascone; beta-danascenone; delta-damascone; gamma-damascone; 1-(2,4,4-trimethyl-2-cyclohexen-1-yl)-2-buten-1-one; 1,3,4,6,7,8a-hexahydro-1,1,5,5-tetramethyl-2H-2,4a-methanonaphthalen-8(5H)-one; nootkatone; dihydronootkatone; acetylated cedarwood oil (cedryl methyl ketone); cyclic alcohols, such as, for example, 4-tert.-butylcyclohexanol; 3,3,5-trimethylcyclohexanol; 3-isocamphylcyclohexanol; 2,6,9-trimethyl-Z2,Z5,E9-cyclododecatrien-1-ol; 2-isobutyl-4-methyltetrahydro-2H-pyran-4-ol; cycloaliphatic alcohols, such as, for example, alpha,3,3-trimethylcyclo-hexyl-methanol; 2-methyl-4-(2,2,3-trimethyl-3-cyclopent-1-yl)butanol; 2-methyl-4-(2,2,3-trimethyl-3-cyclopent-1-yl)-2-buten-1-ol; 2-ethyl-4-(2,2,3-trimethyl-3-cyclopent-1-yl)-2-buten-1-ol; 3-methyl-5-(2,2,3-trimethyl-3-cyclopent-1-yl)-pentan-2-ol; 3-methyl-5-(2,2,3-trimethyl-3-cyclopent-1-yl)-4-penten-2-ol; 3,3-dimethyl-5-(2,2,3-trimethyl-3-cyclopent-1-yl)-4-penten-2-ol; 1-(2,2,6-trimethylcyclohexyl)pentan-3-ol; 1-(2,2,6-trimethylcyclohexyl)hexan-3-ol; cyclic and cycloaliphatic ethers, such as, for example, cineole; cedryl methyl ether; cyclododecyl methyl ether; (ethoxymethoxy)cyclododecane; alpha-cedrene epoxide; 3a,6,6,9a-tetramethyldodecahydronaphtho[2,1-b]furan; 3a-ethyl-6,6,9a-trimethyl-dodecahydronaphtho[2,1-b]furan; 1,5,9-trimethyl-13-oxabicyclo[10.1.0]-trideca-4,8-diene; rose oxide; 2-(2,4-dimethyl-3-cyclohexen-1-yl)-5-methyl-5-(1-methyl-propyl)-1,3-dioxan; cyclic ketones, such as, for example, 4-tert.-butylcyclohexanone; 2,2,5-trimethyl-5-pentylcyclopentanone; 2-heptylcyclopentanone; 2-pentylcyclopentanone; 2-hydroxy-3-methyl-2-cyclopenten-1-one; 3-methyl-cis-2-penten-1-yl-2-cyclopenten-1-one; 3-methyl-2-pentyl-2-cyclopenten-1-one; 3-methyl-4-cyclopentadecenone; 3-methyl-5-cyclopentadecenone; 3-methylcyclopentadecanone; 4-(1-ethoxyvinyl)-3,3,5,5-tetramethylcyclo-hexanone; 4-tert.-pentylcyclohexanone; 5-cyclohexadecen-1-one; 6,7-dihydro-1,1,2,3,3-pentamethyl-4(5H)-indanone; 5-cyclohexadecen-1-one; 8-cyclohexadecen-1-one; 9-cycloheptadecen-1-one; cyclopentadeca-none; cycloaliphatic aldehydes, such as, for example, 2,4-dimethyl-3-cyclohexene carbaldehyde; 2-methyl-4-(2,2,6-trimethyl-cyclohexen-1-yl)-2-butenal; 4-(4-hydroxy-4-methylpentyl)-3-cyclohexene carbaldehyde; 4-(4-methyl-3-penten-1-yl)-3-cyclohexene carbaldehyde; cycloaliphatic ketones, such as, for example, 1-(3,3-dimethylcyclohexyl)-4-penten-1-one; 1-(5,5-dimethyl-1-cyclohexen-1-yl)-4-penten-1-one; 2,3,8,8-tetramethyl-1,2,3,4,5,6,7,8-octahydro-2-naphtalenyl methyl ketone; methyl-2,6,10-trimethyl-2,5,9-cyclododecatrienyl ketone; tert.-butyl-(2,4-dimethyl-3-cyclohexen-1-yl)ketone; esters of cyclic alcohols, such as, for example, 2-tert.-butylcyclohexyl acetate; 4-tert.-butylcyclohexyl acetate; 2-tert.-pentylcyclohexyl acetate; 4-tert.-pentylcyclohexyl acetate; decahydro-2-naphthyl acetate; 3-pentyltetrahydro-2H-pyran-4-yl acetate; decahydro-2,5, 5,8a-tetramethyl-2-naphthyl acetate; 4,7-methano-3a,4,5,6,7,7a-hexa-hydro-5 or 6-indenyl acetate; 4,7-methano-3a,4,5,6,7,7a-hexahydro-5 or 6-indenyl propionate; 4,7-methano-3a,4,5,6,7,7a-hexahydro-5 or 6-indenyl isobutyrate; 4,7-methanooctahydro-5 or 6-indenyl acetate; esters of cycloaliphatic carboxylic acids, such as, for example, allyl 3-cyclohexyl-propionate; allyl cyclohexyl oxyacetate; methyl dihydrojasmo-nate; methyl jasmonate; methyl 2-hexyl-3-oxocyclopentanecarboxylate; ethyl 2-ethyl-6,6-dimethyl-2-cyclohexenecarboxylate; ethyl 2,3,6,6-tetramethyl-2-cyclohexenecarboxylate; ethyl 2-methyl-1,3-dioxolane-2-acetate; araliphatic alcohols, such as, for example, benzyl alcohol; 1-phenylethyl alcohol; 2-phenylethyl alcohol; 3-phenylpropanol; 2-phenylpropanol; 2-phenoxyethanol; 2,2-dimethyl-3-phenylpropanol; 2,2-dimethyl-3-(3-methylphenyl)propanol; 1,1-dimethyl-2-phenylethyl alcohol; 1,1-dimethyl-3-phenylpropanol; 1-ethyl-1-methyl-3-phenylpropanol; 2-methyl-5-phenylpentanol; 3-methyl-5-phenylpentanol; 3-phenyl-2-propen-1-ol; 4-methoxybenzyl alcohol; 1-(4-isopropylphenyl)ethanol; esters of araliphatic alcohols and aliphatic carboxylic acids, such as, for example, benzyl acetate; benzyl propionate; benzyl isobutyrate; benzyl isovalerate; 2-phenylethyl acetate; 2-phenylethyl propionate; 2-phenylethyl isobutyrate; 2-phenylethyl isovalerate; 1-phenylethyl acetate; alpha-trichloromethylbenzyl acetate; alpha,alpha-dimethylphenylethyl acetate; alpha,alpha-dimethylphenylethyl butyrate; cinnamyl acetate; 2-phenoxyethyl isobutyrate; 4-methoxybenzyl acetate; araliphatic ethers, such as for example 2-phenylethyl methyl ether; 2-phenylethyl isoamyl ether; 2-phenylethyl-1-ethoxyethyl ether; phenylacetaldehyde dimethyl acetal; phenylacetaldehyde diethyl acetal; hydratropaaldehyde dimethyl acetal; phenylacetaldehyde glycerol acetal; 2,4,6-trimethyl-4-phenyl-1,3-dioxane; 4,4a,5,9b-tetrahydroindeno[1,2-d]-m-dioxin; 4,4a,5,9b-tetrahydro-2,4-dimethylindeno[1,2-d]-m-dioxin; aromatic and araliphatic aldehydes, such as, for example, benzaldehyde; phenylacetaldehyde; 3-phenylpropanal; hydratropaldehyde; 4-methylbenzaldehyde; 4-methyl-phenylacetaldehyde; 3-(4-ethylphenyl)-2,2-dimethylpropanal; 2-methyl-3-(4-isopropylphenyl)propanal; 2-methyl-3-(4-tert.-butylphenyl)propanal; 3-(4-tert.-butyl-phenyl)propanal; cinnamaldehyde; alpha-butylcinnamaldehyde; alpha-amylcinnamaldehyde; alpha-hexylcinnamaldehyde; 3-methyl-5-phenylpentanal; 4-methoxybenzaldehyde; 4-hydroxy-3-methoxybenzaldehyde; 4-hydroxy-3-ethoxybenzaldehyde; 3,4-methylene-dioxybenzaldehyde; 3,4-dimethoxybenzaldehyde; 2-methyl-3-(4-methoxyphenyl)propanal; 2-methyl-3-(4-methylendioxyphenyl)propanal; aromatic and araliphatic ketones, such as, for example, acetophenone; 4-methylacetophenone; 4-methoxyacetophenone; 4-tert.-butyl-2,6-dimethylacetophenone; 4-phenyl-2-butanone; 4-(4-hydroxyphenyl)-2-butanone; 1-(2-naphthalenyl)ethanone; benzophenone; 1,1,2,3,3,6-hexamethyl-5-indanyl methyl ketone; 6-tert.-butyl-1,1-dimethyl-4-indanyl methyl ketone; 1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methyl-ethyl)-1H-5-indenyl]ethanone; 5′,6′,7′,8′-tetrahydro-3′,5′,5′,6′,8′,8′-hexamethyl-2-acetonaphthone; aromatic and araliphatic carboxylic acids and esters thereof, such as, for example, benzoic acid; phenylacetic acid; methyl benzoate; ethyl benzoate; hexyl benzoate; benzyl benzoate; methyl phenylacetate; ethyl phenylacetate; geranyl phenylacetate; phenylethyl phenylacetate; methyl cinnamate; ethyl cinnamate; benzyl cinnamate; phenylethyl cinnamate; cinnamyl cinnamate; allyl phenoxyacetate; methyl salicylate; isoamyl salicylate; hexyl salicylate; cyclohexyl salicylate; cis-3-hexenyl salicylate; benzyl salicylate; phenylethyl salicylate; methyl 2,4-dihydroxy-3,6-dimethylbenzoate; ethyl 3-phenylglycidate; ethyl 3-methyl-3-phenylglycidate; nitrogen-containing aromatic compounds, such as, for example, 2,4,6-trinitro-1,3-dimethyl-5-tert-butylbenzene; 3,5-dinitro-2,6-dimethyl-4-tert.-butylacetophenone; cinnamonitrile; 5-phenyl-3-methyl-2-pentenonitrile; 5-phenyl-3-methylpentanonitrile; methyl anthranilate; methyl-N-methylanthranilate; Schiff's bases of methyl anthranilate with 7-hydroxy-3,7-dimethyloctanal, 2-methyl-3-(4-tert.-butylphenyl)-propanal or 2,4-dimethyl-3-cyclohexene carbaldehyde; 6-isopropylquinoline; 6-isobutylquinoline; 6-sec.-butylquinoline; indole; skatole; 2-methoxy-3-isopropyl-pyrazine; 2-isobutyl-3-methoxypyrazine; phenols, phenyl ethers and phenyl esters, such as, for example, estragole; anethole; eugenol; eugenyl methyl ether; isoeugenol; isoeugenol methyl ether; thymol; carvacrol; diphenyl ether; beta-naphthyl methyl ether; beta-naphthyl ethyl ether; beta-naphthyl isobutyl ether; 1,4-dimethoxybenzene; eugenyl acetate; 2-methoxy-4-methylphenol; 2-ethoxy-5-(1-propenyl)phenol; p-cresyl phenylacetate; heterocyclic compounds, such as, for example, 2,5-dimethyl-4-hydroxy-2H-furan-3-one; 2-ethyl-4-hydroxy-5-methyl-2H-furan-3-one; 3-hydroxy-2-methyl-4H-pyran-4-one; 2-ethyl-3-hydroxy-4H-pyran-4-one; lactones, such as, for example, 1,4-octanolide; 3-methyl-1,4-octanolide; 1,4-nonanolide; 1,4-decanolide; 8-decen-1,4-olide; 1,4-undecanolide; 1,4-dodecanolide; 1,5-decanolide; 1,5-dodecanolide; 1,15-pentadecanolide; cis- and trans-11-pentadecen-1,15-olide; cis- and trans-12-pentadecen-1,15-olide; 1,16-hexadecanolide; 9-hexadecen-1,16-olide; 10-oxa-1,16-hexadecanolide; 11-oxa-1,16-hexadecanolide; 12-oxa-1,16-hexadecanolide; ethylene-1,12-dodecanedioate; ethylene-1,13-tridecanedioate; coumarin; 2,3-dihydrocoumarin; octahydrocoumarin.
Especially suitable lemon fragrances are limonenal (3-(4-methyl-3% cyclohexenyl)butanal), limonene (4-isopropenyl-1-methylcyclohexene), lemon oil, and lemonal (3,7-dimethyl-2,6-octadienal).
Malodors are usually caused by particularly odorous substances which are, however, frequently only present in trace amounts. Such substances include, for example, nitrogen-containing compounds such as ammonia and amines, heterocyclic compounds such as pyridines, pyrazines, indoles, etc. and sulfur-containing compounds such as hydrogen sulfide, mercaptans, sulfides, acidic compounds such as acetic acid, butyric acid and fatty acids, and aldehyde compounds such as acetaldehyde and formaldehyde. The masking of malodors is a problem, which is difficult to handle and solve with perfume compositions. The specific unique quality of a malodor greatly restricts the use of perfumes having the various types of commonly known fragrances. Usually, it is only possible to mask malodors by means of a specially developed perfume oil having a very specific type of fragrance. Active ingredients are, therefore, particularly advantageous when they are capable of reducing the intensity of malodors without themselves possessing any significantly intense odor or fragrance. Such active ingredients do not mask malodors but neutralize them. This has the advantage that when using such active ingredients for perfuming objects or products with malodors, perfume oils of any desired type of fragrance can be used. The consumer can, therefore, be offered a considerably broader range of fragrance types for combating malodors. In addition, active ingredients, which neutralize malodors, provide the possibility of reducing the quantity of perfume oil previously required for masking odors. It is also possible to use less intensely odorous perfumes for combating malodors than those so far employed, which sometimes have an overpowering effect due to their high intensity.
Suitable malodor control compounds are the general classification of musk compounds. These include Galaxolide™ (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-2-benzopyran), Traseolide™ (6-acetyl-1-isopropyl-2,3,3,5-tetramethylindane), Ambrettolide (cyclohexadecen-7-olide), Celestolide (4-Acetyl-6-tert-butyl-1,1-dimethylindane), Dihydroambrettolide (cyclohexadecanolide), Ethylene brassylate (cyclo-1,13-ethylenedioxy-tridecan-1,13-dione), Exaltolide (cyclopentadecanolide), Exaltone (cyclopentadecanone), Moskene (1,1,3,3,5-Pentamethyl-4,6-dinitroindane), Musk ambrette (2,4-dinitro-3-methyl-6-tert-butylanisole), Musk Ketone (4-tert-butyl-3,5-dinitro-2,6-dimethylacetophenone), Musk MC4 (ethylene 1,12-dodecanedioate), Musk R1 (11-Oxahexadecanolide), Musk tibetine (2-tert-butyl-1,3-dinitro-4,5,6-trinitrobenzene), Musk xylol (1-tert-butyl-3,5-dimethyl-2,4,6-trinitrobenzene), Phentolide (5-Acetyl-1,1,2,3,3,6-hexamethylindane), Tonalid (1,1,2,4,4,7-hexamethyl-6-acetyl-1,2,3,4-tetrahydronaphthalene), versalide (1,1,4,4-tetramethyl-6-acetyl-7-ethyl-1,2,3,4-tetrahydronaphthalene).
Additional suitable malodor control agents are found in WO2009/131748 to Conover, describing a multiple component compound containing a molecular encapsulator, Ordenone, and an aromatic complex, such as citronellal and hydroxycitronellal. Additional useful compounds are aldehydes and their complexes, such as aldehydes and complexes of decanal; undecanal; dodecanal; undecene-10-al; 2-methyl-undecanal; 2,3,5,5-tetramethylhexanal; 1-formyl-2,4-dimethyl-2-cyclohexene; 1-formyl-3,5-dimethyl-4-cyclohexene; 1-formyl-2,3,5-trimethyl-4-cyclohexene; 1-formyl-2,4,6-trimethyl-3-cyclohexene; ([5.2.1.0]-tricyclo-8-decylidene)-4-butanal; 2,6,10-trimethyl-9-undecenal; (4-methyl-3-pentenyl)-cyclohexene-3-yl carboxaldehyde; 7-formyl-5-isopropyl-2-methyl-[2.2.2]-bicyclo-2-octene; 2-formyl-8-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene; citronellal; campholenic aldehyde; α-methyl-3,4-methylenedioxyhydrocinnamic aldehyde; cyclamen aldehyde; lilial; canthoxal; phenylacetic aldehyde; 3-phenylpropionic aldehyde; hydratropic aldehyde; α-methyl-3,4-methylenedioxyhydrocinnamic aldehyde; 3-phenylpropionic aldehyde; hydratropic aldehyde; alkoxyacetaldehydes; ω-hydroxyaldehydes; myrtenal; perilla aldehyde; substituted 2-furyl carboxaldehydes; cinnamic aldehyde; amylcinnamic aldehyde; hexylcinnamic aldehyde; benzaldehyde; anisic aldehyde; heliotropine; veratric aldehyde; vanillin; isovanillin; and ethylvanillin. Suitable nitriles are described in U.S. Pat. No. 6,180,814 to Giersch and WO2008/026140 to Tranzeat such as 3-phenyl-2-propenenitrile, citronitrile, geranyl nitrile, cytronellyl nitrile, 2-propyl-1-heptanenitrile, dodecanenitrile, 3-(2,3-dimethyl-2(3)-cyclopenten-1-yl)butanenitrile and 3-(2-methyl-3-methylene-1-cyclopentyl)butanenitrile. Additional suitable malodor control agents are found in U.S. Pat. No. 6,432,891 to O'Connor and include cyclohexyl and phenoxy substituted esters, such as 1-cyclohexyl-ethyl-butyrate, 1-cyclohexyl-ethyl-acetate, 1-cyclohexyl-ethanol, 4-isopropyl-cyclohexyl-propionate, phenoxyacetic acid 2-hydroxy-ethyl ester.
The film may include a fragrance release inhibitor in the same layer as the fragrance and malodor control agents. A typical fragrance release inhibitor is titanium dioxide. Additional fragrance release inhibitors include starch, clays and nanoclays, talc, and microcapsules.
All references, including publications, patent applications, and patents, cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.
The use of the terms “a” and “an” and “the” and similar referents in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The terms “comprising,” “having,” “including,” and “containing” are to be construed as open-ended terms (i.e., meaning “including, but not limited to,”) unless otherwise noted. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided herein, is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.
Preferred embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. Variations of those preferred embodiments may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors expect skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context.
Claims
1. A thermoplastic bag comprising:
- a first sidewall of pliable thermoplastic material;
- a second sidewall of pliable thermoplastic material overlaying and joined to the first sidewall along a first side edge, an opposite second side edge, and a bottom edge extending between the first and second side edges to provide an interior volume, the interior volume accessible by an opening provided by first and second top edges of the respective first and second sidewalls;
- wherein the length of the first and second top edges in the relaxed state are less that the length of the bottom edge;
- a draw tape in a first hem formed proximate the first top edge, the draw tape attached to the bag at the first and second side edges, a second draw tape in a second hem formed proximate the second top edge, the second draw tape attached to the bag at the first and second side edges;
- wherein the first and second hems enclose a hem area and the hem area comprises a fragrance.
2. The thermoplastic bag of claim 1, wherein the hem area additionally comprises a malodor control agent.
3. The thermoplastic bag of claim 1, wherein the hem area additionally comprises a fragrance release inhibitor.
4. The thermoplastic bag of claim 1, wherein the fragrance is concentrated in the hem area.
5. The thermoplastic bag of claim 1, wherein the fragrance comprises greater than 20 percent fragrance ingredients with ClogP of greater than 4.
6. A thermoplastic bag comprising:
- a first sidewall of pliable thermoplastic material;
- a second sidewall of pliable thermoplastic material overlaying and joined to the first sidewall along a first side edge, an opposite second side edge, and a bottom edge extending between the first and second side edges to provide an interior volume, the interior volume accessible by an opening provided by first and second top edges of the respective first and second sidewalls;
- wherein the bag includes a first hem and a draw tape in the first hem, wherein the hem is substantially enclosed from the interior volume;
- wherein the length of the hem in the relaxed state is less than the length of the bottom edge; and
- wherein the hem comprises a fragrance, a malodor control agent, and a fragrance release inhibitor
7. The thermoplastic bag of claim 6, wherein the hem has three or more layers of pliable thermoplastic material wherein the layers include an exterior layer, a central layer, and an interior layer wherein the central layer of the hem area comprises a fragrance, a malodor control agent, and a fragrance release inhibitor.
8. The thermoplastic bag of claim 6, wherein the fragrance comprises a compound selected from the group consisting of 1,1-Dimethoxy-2,2,5-trimethylhex-4-ene, N-methyl-N-phenyl-2-methylbutanamide, 1-p-methene-8-thiol, thiobenzoic acids, 2,4,6-trimethyl-4-phenyl-1,3-dioxane, 2,6-dimethyl-6-(3-methyl-but-2-enyl)-cyclo-hex-2-enone, 2,4,6-trimethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enone, 2,2,6-trimethyl-6-(3-methyl-but-2-enyl)-cyclohex-3-enone, 2,6-Dimethyl-2-(3-methyl-but-2-enyl)-cyclohexanone, 1,2,6-trimethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enol, 6-methoxy-1,5,6-trimethyl-5-(3-methyl-but-2-enyl)-cyclohexene, 1,2,4,6-Tetramethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enol, 2,6-Dimethyl-6-(3-methyl-but-2-enyl)-1-vinyl-cyclohex-2-enol, 2,6-Dimethyl-1-ethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enol, 2,6-dimethyl-6-(3-methyl-but-2-enyl)-cyclo-hex-2-enol, 1,2,6-Trimethyl-6-(3-methyl-but-2-enyl)-cyclohexa-2,4-dienol, and 2-(2,3-Dimethyl-but-2-enyl)-2,6-dimethyl-cyclohexanone and mixtures thereof.
9. The thermoplastic bag of claim 8, wherein the fragrance release inhibitor comprises titanium dioxide.
10. The thermoplastic bag of claim 6, wherein the fragrance comprises a compound selected from the group consisting of acetanisole, anisyl acetate, anisyl alcohol, anisyl propionate, benzoin, cinnamaldehyde, ethyl vanillin, 2-methoxy-4-methylphenol, 1-(p-methoxyphenyl)-2-propanone, propenyl guaethol, veratraldehyde, vanillylacetone, vanillin isobutyrate, veratrole, acetovanillone and mixtures thereof.
11. The thermoplastic bag of claim 10, wherein the fragrance release inhibitor comprises titanium dioxide.
12. The thermoplastic bag of claim 6, wherein the malodor control agent comprises a musk compound.
13. The thermoplastic bag of claim 12, wherein the musk compound comprises a compound selected from the group consisting of 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-2-benzopyran, 6-acetyl-1-isopropyl-2,3,3,5-tetramethylindane, Ambrettolide (cyclohexadecen-7-olide), Celestolide (4-Acetyl-6-tert-butyl-1,1-dimethylindane), Dihydroambrettolide (cyclohexadecanolide), Ethylene brassylate (cyclo-1,13-ethylenedioxy-tridecan-1,13-dione), Exaltolide (cyclopentadecanolide), Exaltone (cyclopentadecanone), Moskene (1,1,3,3,5-Pentamethyl-4,6-dinitroindane), Musk ambrette (2,4-dinitro-3-methyl-6-tert-butylanisole), Musk Ketone (4-tert-butyl-3,5-dinitro-2,6-dimethylacetophenone), Musk MC4 (ethylene 1,12-dodecanedioate), Musk R1 (11-Oxahexadecanolide), Musk tibetine (2-tert-butyl-1,3-dinitro-4,5,6-trinitrobenzene), Musk xylol (1-tert-butyl-3,5-dimethyl-2,4,6-trinitrobenzene), Phentolide (5-Acetyl-1,1,2,3,3,6-hexamethylindane), Tonalid (1,1,2,4,4,7-hexamethyl-6-acetyl-1,2,3,4-tetrahydronaphthalene), versalide (1,1,4,4-tetramethyl-6-acetyl-7-ethyl-1,2,3,4-tetrahydronaphthalene), and combinations thereof.
14. A thermoplastic bag comprising:
- a first sidewall of pliable thermoplastic material;
- a second sidewall of pliable thermoplastic material overlaying and joined to the first sidewall along a first side edge, an opposite second side edge, and a bottom edge extending between the first and second side edges to provide an interior volume, the interior volume accessible by an opening provided by first and second top edges of the respective first and second sidewalls;
- a draw tape in a first hem formed proximate the first top edge, the draw tape attached to the bag at the first and second side edges, a second draw tape in a second hem formed proximate the second top edge, the second draw tape attached to the bag at the first and second side edges, wherein one of the draw tapes comprises a fragrance.
15. The thermoplastic bag of claim 14, wherein the fragrance comprises a compound selected from the group consisting of 1,1-Dimethoxy-2,2,5-trimethylhex-4-ene, N-methyl-N-phenyl-2-methylbutanamide, 1-p-methene-8-thiol, thiobenzoic acids, 2,4,6-trimethyl-4-phenyl-1,3-dioxane, 2,6-dimethyl-6-(3-methyl-but-2-enyl)-cyclo-hex-2-enone, 2,4,6-trimethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enone, 2,2,6-trimethyl-6-(3-methyl-but-2-enyl)-cyclohex-3-enone, 2,6-Dimethyl-2-(3-methyl-but-2-enyl)-cyclohexanone, 1,2,6-trimethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enol, 6-methoxy-1,5,6-trimethyl-5-(3-methyl-but-2-enyl)-cyclohexene, 1,2,4,6-Tetramethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enol, 2,6-Dimethyl-6-(3-methyl-but-2-enyl)-1-vinyl-cyclohex-2-enol, 2,6-Dimethyl-1-ethyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enol, 2,6-dimethyl-6-(3-methyl-but-2-enyl)-cyclo-hex-2-enol, 1,2,6-Trimethyl-6-(3-methyl-but-2-enyl)-cyclohexa-2,4-dienol, and 2-(2,3-Dimethyl-but-2-enyl)-2,6-dimethyl-cyclohexanone and mixtures thereof.
16. The thermoplastic bag of claim 14, wherein the fragrance comprises a compound selected from the group consisting of acetanisole, anisyl acetate, anisyl alcohol, anisyl propionate, benzoin, cinnamaldehyde, ethyl vanillin, 2-methoxy-4-methylphenol, 1-(p-methoxyphenyl)-2-propanone, propenyl guaethol, veratraldehyde, vanillylacetone, vanillin isobutyrate, veratrole, acetovanillone and mixtures thereof.
17. The thermoplastic bag of claim 14, wherein the draw tape additionally comprises a fragrance release inhibitor.
18. The thermoplastic bag of claim 17, wherein the fragrance release inhibitor comprises titanium dioxide.
19. The thermoplastic bag of claim 14, wherein the draw tape additionally comprises a malodor control agent.
20. The thermoplastic bag of claim 19, wherein the malodor control agent comprises a musk compound.
Type: Application
Filed: Dec 14, 2010
Publication Date: Jul 7, 2011
Applicant: The Glad Products Company (Oakland, CA)
Inventors: Jeffrey S. Stiglic (New Lenox, IL), Ryan J. Coonce (Palatine, IL)
Application Number: 12/968,081
