Dispensing devices are used to dispense a variety of products. Many dispensers use an aerosol propellant to dispense product from the dispensers. However, there is a desire for a dispensing device having desired spray characteristics that discharges a non-propellant product.
An aspect of the present disclosure relates to a dispenser. The dispenser includes a housing having a sidewall with a first axial end and a second axial end. A container has a first end portion and a second end portion with the second end portion engaged with the housing such that the container extends from the first axial end of the housing. The container defines an interior cavity adapted for containing a product. A plunger is disposed in the interior cavity of the container. The plunger includes a base having a first side and a second side. The interior cavity of the container and the first side of the base cooperatively define a product cavity. The interior cavity of the container and the second side of the base cooperatively define an air cavity. A valve mechanism is in engagement with the second end portion of the container. The valve mechanism includes a nozzle defining an orifice and an accumulator defining a pumping chamber. The pumping chamber is adapted to receive a portion of the product in the container. A piston is selectively slidable in the pumping chamber. The displacement of the piston in one direction increases a pressure of the portion of the product in the pumping chamber to a dispensing pressure.
Another aspect of the present disclosure relates to a dispenser. The dispenser includes a housing having a sidewall with a first axial end and a second axial end. A container has a first end portion and a second end portion with the second end portion engaged with the housing such that the container extends from the first axial end of the housing. The container defines an interior cavity adapted for containing a product. The product is a non-propellant cooking spray composition comprising an edible oil or mixture of edible oils, a pan release agent and a thinning agent. The composition comprises by weight about 60% to about 99% edible oil or mixture of edible oils, about 0% to about 15% thinning agent, and about 1% to about 15% pan release agent. A plunger is disposed in the interior cavity of the container. The plunger includes a base having a first side and a second side. The interior cavity of the container and the first side of the base cooperatively define a product cavity. The interior cavity of the container and the second side of the base cooperatively define an air cavity. A valve mechanism is in engagement with the second end portion of the container. The valve mechanism includes a nozzle defining an orifice and an accumulator defining a pumping chamber. The pumping chamber is adapted to receive a portion of the product in the container. A piston is selectively slidable in the pumping chamber. The displacement of the piston in one direction increases a pressure of the portion of the product in the pumping chamber to a dispensing pressure.
Reference will now be made in detail to the exemplary aspects of the present disclosure that are illustrated in the accompanying drawings. Wherever possible, the same reference numbers will be used throughout the drawings to refer to the same or like structure.
Referring now to
The container 12 includes a first end portion 16 and a second end portion 18. The second end portion 18 of the container 12 tapers down to an outer diameter that is less than an outer diameter of the first end portion 16. It will be understood, however, that the scope of the present disclosure is not limited to the second end portion 18 having an outer diameter that is less than the first end portion 16 as the outer diameter of the first end portion 16 can be less than or equal to the second end portion 18.
The container 12 includes an end wall 20, which is disposed at the first end portion 16, and a sidewall 22, which is disposed about the periphery of the end wall 20. The sidewall 22 extends outwardly from the end wall 20. In the depicted example, the end wall 20 and the sidewall 22 are monolithic.
The end wall 20 and the sidewall 22 of the container 12 define an interior cavity 24 (shown in
A valve mechanism, generally designated 28, is disposed in the opening 26 of the interior cavity 24. The interior cavity 24 of the container 12 and the valve mechanism 28 can be adapted to contain non-aerosol products (e.g., cooking oils, gels, etc.). In order to contain these products, the container 12 can be manufactured from natural or synthetic materials such as aluminum, stainless steel, or various plastics such as polyethylene terephthalate (PET), polytetrafluoroethylene (PTE), polyethylene Naphthalate (PEN), high-density polyethylene, and combinations thereof.
In the depicted example of
The plunger 30 keeps the product cavity 37 and the air cavity 39 separate. This separation of the product in the product cavity 37 from air in the air cavity 39 protects the product stored in the container 12 from exposure to moisture and oxygen. As interactions between the product and moisture and oxygen in the air can form precipitates or can change the fluid viscosity of the product, the plunger 30 provides consistent and repeatable spray characteristics of the dispenser 10 throughout its use and provides a consistent product contained in the dispenser 10 throughout its use. As the plunger 30 protects the product against oxidation and hydration, the use of preservatives such as antioxidants in food related products may be decreased. Therefore, the plunger 30 is potentially advantageous as it provides a cost effective way of keeping the product separate from air. In addition, the plunger 30 allows the product to be seen through a transparent or translucent container 12 so that a consumer can determine the level of product remaining in the container 12.
As the axial position of the plunger 30 changes, air passes into or out of the air cavity 39 through a vent 38 defined by the end wall 20 of the container 12. The size of the vent 38 is dependent upon the velocity of the plunger 30 in the interior cavity 24. In the depicted example shown in
In the depicted example, the container 12 includes an over-cap 42. The over-cap 42 is inserted over the first end portion 16 of the container 12 such that a hole 44 defined in the over-cap 42 is aligned with the vent 38 of the end wall 20. In one example, the over-cap 42 is in friction-fit engagement with the first end portion 16 of the container 12. In another example, the over-cap 42 is bonded to the first end portion 16 with an adhesive.
Referring now to
The container portion 50 of the accumulator 46 is engaged with the second end portion 18 of the container 12. In one example, the container portion 50 is threadedly engaged with the second end portion 18 of the container 12. In another example, the container portion 50 is in snap-fit engagement with the second end portion 18 of the container 12. In another example, the container portion 50 is bonded to the second end portion 18 of the container 12.
The accumulator 46 further includes a pumping chamber 54 disposed between the container portion 50 and the nozzle portion 52. The pumping chamber 54 includes a container end 56 and an oppositely disposed nozzle end 58. In the depicted example, a cylindrical wall 60 extends outwardly from the nozzle end 58 toward the container end 56 and defines an axial opening 62 in fluid communication with the container portion 50 and the nozzle portion 52 of the accumulator 46.
A piston, generally designated 64, is disposed in the pumping chamber 54 of the accumulator 46. In the depicted embodiment, the piston 64 is selectively slidable in the pumping chamber 54. The piston 64 includes a body, generally designated 66, having a first end 68, which faces toward the container end 56, and a second end 70, which faces toward the nozzle end 58. A stem portion 72 extends outwardly from the first end 68 of the body 66 while a valve portion 74 extends outwardly from the second end 70. The stem portion 72 defines a bore 76 that extends into a cavity 78 defined by the body 66. The valve portion 74 of the piston 64 is a one-way valve that is biased to a closed position. While the one-way valve 74 is disposed on the piston 64 in the depicted embodiment, it will be understood that the scope of the present disclosure is not limited to the one-way valve 74 being disposed in the piston 64 as the one-way valve 74 could be disposed in an alternate location in the accumulator 46 or in the second end portion 18 of the container 12.
The nozzle portion 52 of the accumulator 46 is engaged with a nozzle tube, generally designated 90. The nozzle tube 90 includes a first axial end 92 and an oppositely disposed second axial end 94 and defines a central opening 96 through the first and second axial ends 92, 94. The first axial end 92 of the nozzle tube 90 is in engagement with the nozzle portion 52 of the accumulator 46. In one example, the nozzle portion 52 is threadedly engaged with the first axial end 92 of the nozzle tube 90. In another example, the nozzle portion 52 is bonded to the first axial end 92 of the nozzle tube 90. In another example, the nozzle tube 90 is in press-fit engagement with the first axial end 92 of the nozzle tube 90.
The nozzle 48 is engaged with the second axial end 94 of the nozzle tube 90. In the depicted example, the nozzle 48 includes an insert 100 that defines an orifice 102. A pressure chamber 104, which is disposed between the valve portion 74 of the piston 64 and the orifice 102 of the nozzle 48, is cooperatively defined by the cylindrical wall 60 of the accumulator 46, the nozzle tube 90, and the nozzle 48.
Referring now to
The housing 120 defines a central cavity 130 (shown in
The dispensing device 14 further includes an actuator, generally designated 134. In the depicted example, the actuator 134 is pivotally engaged with the sidewall 122 of the housing 120. It will be understood, however, that the scope of the present disclosure is not limited to the actuator 134 being pivotally engaged with the sidewall 122.
The actuator 134 includes a handle portion 136 and an actuation portion 138. In the depicted example, the handle portion 136 defines a pivot opening 140. The pivot opening 140 is adapted to receive a pin that is inserted through pin openings 142 in the sidewall 122 of the housing 120 and through the pivot opening 140 in the actuator 134. An outer diameter of the pin is slightly smaller than the inner diameter of the pivot opening 140 in the actuator 134 which allows for the actuator 134 to pivot about the pin between a released position (shown in
The actuation portion 138 of the actuator 134 extends through the sidewall 122 of the housing 120 and through an exterior of the accumulator 46. An end 144 of the actuator portion 138 engages a shoulder 146 disposed on the body 66 of the piston 64. As the actuator 134 is pivoted about the pin toward the housing 120, the end 144 of the actuator portion 138 displaces the piston 64 downwardly toward the nozzle 48. When the actuator 134 is released, a spring 148 that is disposed in the pumping chamber 54 of the accumulator 46 biases the piston 64 in an upward direction, which pivots the actuator 134 about the pin to the released position.
Referring now to
As product is drawn into the pressure chamber 104, the product volume in the container 12 decreases. As the product volume decreases, the plunger 30, which is disposed in the container 12, is pulled downwardly toward the second end portion 18 of the container 12 by suction. As the plunger 30 is pulled downwardly, air enters the air cavity 39 in the container 12 through the vent 38 in the end wall 20.
Referring now to
The size of the orifice 102 of the nozzle 48 is chosen based on fluid pressure and fluid viscosity. In one example, the size of the orifice 102 of the nozzle 48 is based on the fluid pressure of the product in the pressure chamber 104 immediately prior to product dispensing being about 80 psi to about 120 psi, about 90 psi to about 110 psi, or about 100 psi.
As previously stated, the container 12 can be adapted to contain various liquids, gels, and gases. However, it is particularly advantageous when used with liquids such as non-propellant cooking spray compositions. Non-propellant cooking spray compositions for use in the dispenser 10 and methods for preparing the cooking spray compositions will now be described.
The cooking spray compositions are capable of facilitating the release of foodstuffs from cookware and cooking utensils. The non-propellant cooking spray compositions have a viscosity of about 25 centipoise (cPs) to about 45 cPs and comprise an edible oil or mixture of edible oils, a pan release agent, and a thinning agent. The non-propellant compositions can optionally include one or more preservatives, flavorings, and/or colorants. The cooking spray composition is generally transparent or translucent and substantially free of foam.
Any edible oil or mixture or blend of edible oils can be used in the compositions. The edible oil can be a vegetable oil, animal oil, or nut oil. Such oils include, but are not limited to, canola, partially hydrogenated winterized canola, corn, coconut, palm, sesame, olive, peanut, cottonseed, safflower, soy, partially hydrogenated winterized soy, sunflower, almond, cashew, hazelnut, macadamia, pecan, pistachio, walnut, grape seed, pumpkin seed, watermelon seed, fish, and rice bran oils. The edible oil can be extracted from animal or plant tissues, fruits, or seeds using conventional methods.
As used herein, the terms “percent by weight” and “% by weight” used with reference to a particular component means the weight of that component in the composition divided by the total weight of the composition, including that of the particular component, with the result multiplied by 100. The edible oil component of the non-propellant cooking spray compositions constitutes by percentage the largest component by weight of the composition and serves as a vehicle for the pan release agent and any other ingredients. The edible oil or mixture thereof comprises about 60% to about 99%, about 65% to about 99%, about 70% to about 99%, about 75% to about 99%, about 76% to about 99%, about 77% to about 99%, about 78% to about 99%, about 79% to about 99%, about 80% to about 99%, about 85% to about 99%, about 90% to about 99%, about 95% to about 99%, about 96% to about 99%, about 97% to about 99%, or about 98% to about 99% by weight of the cooking spray composition. In some of the compositions, the edible oil comprises about 60% to about 90%, about 70% to about 90%, about 75% to about 90%, about 76% to about 90%, about 77% to about 90%, about 78% to about 90%, about 79% to about 90%, about 80% to about 90%, or about 85% to about 90% by weight of the cooking spray composition. In some of the compositions, the edible oil comprises about 70% to about 80%, about 75% to about 80%, about 76% to about 80%, about 77% to about 80%, about 78% to about 80%, or about 79% to about 80%, or by weight of the composition. In some of the compositions, the edible oil comprises, about 70%, about 71%, about 72%, about 73%, about 74%, about 75%, about 76%, about 77%, about 78%, about 79%, about 80%, about 81% about 82%, about 83%, about 84%, about 85%, about 86%, about 87%, about 88%, about 89%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% be weight of the composition.
The pan releasing agent of the non-propellant cooking spray compositions comprises lecithin, phosphated monoglycerides, phosphated diglycerides, a lecithin replacer such as NU-RICE® (Ribus, St. Louis, Mo.), or a combination thereof. Any lecithin, including commercially available standard lecithins, modified lecithins and combinations thereof, may be used in the composition. As used herein, the term “standard lecithin” means any lecithin whether crude, refined, filtered, and/or bleached wherein the lecithin, or at least the phosphatide content thereof, is not chemically modified by reaction of its functional groups. As used herein, “modified lecithin” mean chemically modified lecithins, such as acetylated and hydroxylated lecithins.
Any phosphated monoglyceride and/or diglyceride may be used alone or in combination in the composition. Phosphated monoglycerides and phosphated diglycerides are commercially available, for example, from Lambent Technologies (Gurnee, Ill.) and Magrabar Chemical (Morton Grove, Ill.). Examples of commercially available phosphated monoglycerides and phosphated diglycerides include, but are not limited to, LAMCHEM™ PE-130K, LAMCHEM™ 113 (Lambent Technologies, Gurnee, Ill.), and Phosphoglyceride GPC-10-CSO-LA (Magrabar Chemical, Morton Grove, Ill.).
The pan releasing agent comprises about 1% to about 15%, about 2% to about 15%, bout 3% to about 15%, about 4% to about 15%, about 6% to about 15%, about 7% to about 15%, about 8% to about 15%, about 9% to about 15%, about 10% to about 15%, about 11% to about 15%, about 12% to about 15%, about 13% to about 15%, or about 14% to about 15% by weight of the composition. In some of the compositions, the pan releasing agent comprises 2.5% to about 6%, about 3% to about 6%, about 3.5% to about 6%, about 4% to about 6%, about 4.5% to about 6%, about 5% to about 6% by weight of the cooking spray composition. In some of the compositions, the pan releasing agent comprises about 2% to about 5.5%, about 2.5% to about 5.5%, about 3% to about 5.5%, about 3.5% to about 5.5%, about 4% to about 5.5%, about 4.5% to about 5.5%, or about 5% to about 5.5% by weight of the cooking spray composition. In some of compositions, the pan releasing agent comprises about 2% to about 6%, about 2.5% to about 6% about, 3% to about 6%, about 3.5% to about 6%, about 4% to about 6%, or about 4.5% to about 6%, about 5% to about 6%, or about 5.5% to about 6% by weight of the cooking spray composition. In some of the compositions, the pan releasing agent comprises about 2% to about 3.5%, about 2.5% to about 3.5%, or about 3% to about 3.5% by weight of the cooking spray composition. In some of the compositions, the pan releasing agent comprises about 2% to about 3%, about 2.5% to about 3%, or about 2.75% to about 3% by weight of the cooking spray composition. In some of the compositions, the pan releasing agent comprises about 2%, about 2.1%, about 2.2%, about 2.3%, about 2.4%, about 2.5%, about 2.6%, about 2.7% about, 2.8%, about 2.9%, or about 3% by weight of the cooking spray composition. In some of the compositions, the pan releasing agent comprises about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 11%, about 12%, about 13%, about 14%, or about 15% by weight of the cooking spray composition. In some of the compositions, the pan releasing agent comprises about 3%, about 3.25%, about 3.5%, about 3.75%, about 4%, about 4.25%, about 4.5%, about 4.75%, about 5%, about 5.25%, about 5.5%, about 5.75%, or about 6% by weight of the cooking spray compositions.
The amount of lecithin is calculated as unhydrated lecithin. Thus the amount of lecithin when expressed as percent by weight of the cooking spray composition is specified independently of water content, whether the water is present as free water, water of hydration, or as both.
The lecithin is generally obtained from soybeans, rice, or egg yolk. The lecithin can be in liquid or powder form. Most commercially available lecithins are made from soybeans and are available both in liquid form or dry powdered form. The liquid form is usually dissolved in soybean oil or other edible oil. Food grade lecithins are typically obtained from soybeans by mixing soybean oil with water, which hydrates the lecithin and renders it substantially insoluble in the soybean oil, thereby permitting centrifugal separation of the hydrated lecithin from the oil. The separated lecithin may be dried to provide a lecithin powder or redissolved in a suitable edible oil to provide the lecithin in liquid form.
Lecithin is a complex mixture of acetone-insoluble phosphatides comprised mostly of phosphatidylcholine and lesser amounts of phosphatidylethanolamine and phosphatidylinositol, and varying amounts of other materials such as triglycerides, fatty acids, and carbohydrates. Commercially available lecithins are available containing the above components in various combinations and proportions, usually containing from about 50 to 65 percent by weight of acetone-insolubles (phosphatides). In liquid form, lecithin is usually dissolved in soybean oil and is available in different viscosities. The lecithin can be bleached or unbleached and filtered or otherwise refined. Bleaching lightens the color of lecithin and is typically carried out using peroxides. Such treatments typically do not chemically alter the phosphatide content of the lecithin.
The lecithin can be chemically modified. Lecithin contains different functional groups that make it reactive in a number of chemical reactions. Chemically modified lecithins include lecithins which have been acetylated, hydroxylated, hydrolyzed, hydrogenated, halogenated, phosphorylated and sulfonated, among other treatments. However, insofar as significant quantities of commercially available chemically modified lecithins are concerned, only acetylated and hydroxylated lecithins are widely commercially available.
The lecithin may contain a small amount of fatty acids. Generally manufacturers of commercial lecithins add small amounts of fatty acids to their products in order to produce end product lecithins that have consistent pH values and/or to control the viscosity of the lecithin. Since lecithins naturally contain varying quantities of fatty acids, the amounts of fatty acids added by the lecithin manufacturers varies as well.
The thinning agent of the non-propellant cooking spray compositions comprises medium chain triglycerides (MCT), ethyl alcohol, or a combination thereof. MCTs are medium chain (e.g., 6 to 12 carbons) fatty acid esters of glycerol. Coconut oil and palm kernel oils are several common sources for MCTs. The medium chain fatty acids (and the corresponding number of carbon atoms) found in MCTs are caproic (C6), caprylic (C8), capric (C10), and lauric acid (C12). MCTs are composed of a glycerol backbone and three of these fatty acids, and are commonly expressed as approximate ratios of these fatty acids. For example, a commercial MCT that can be derived from coconut oil is 2(C6):55(C8):42(C10):1(C12) (see, for example, www.pdrhealth.com/drug_info/nmdrugprofiles/nutsupdrugs/med—0172.html). Any MCT or mixtures thereof can be used in the non-propellant cooking spray compositions. Examples of useful MCTs include, but are not limited to, 1(C6):68(C8):30(C10):1(C12), 56(C8):44(C10), 4(C8):96(C10), 97(C8):3(C10), 1(C6):68(C8):30(C10):1(C12), 6(C6):55.5-85(C8):15-40(C10):4(C12), and 2(C6):55(C8):42(C10):1(C12). Food grade MCTs are commercially available, for example, from Stepan Co. (Northfield, Ill.), Lambent Technologies (Gurnee, Ill.) and Abitec Corp. (Columbus, Ohio). Commercially available MCTs useful in the non-propellant cooking spray compositions described herein include, but are not limited to, CAPTEX® 350 (Abitec Corp., Columbus, Ohio), LUMULSE® CC-33 FKG (Lambent Technologies, Gurnee, Ill.), NEOBEE® 895 (Stepan Co., Northfield, Ill.), NEOBEE® 1053 (Stepan Co., Northfield, Ill.), NEOBEE® 1095 (Stepan Co., Northfield, Ill.), NEOBEE® M-5 (Stepan Co., Northfield, Ill.), and NEOBEE® M-20 (Stepan Co., Northfield, Ill.).
Ethyl alcohol may be included in some of the non-propellant cooking spray compositions as a thinning agent alone or in combination with an MCT. The ethyl alcohol comprises pure grain ethyl alcohol, 160 proof ethyl alcohol, 170 proof ethyl alcohol, 180 proof ethyl alcohol, 190 proof ethyl alcohol, or 200 proof ethyl alcohol.
The amount of thinning agent, particular thinning agent, or mixture of thinning agents utilized in the non-propellant cooking spray compositions is dependent on the desired viscosity of the composition, the viscosity of the edible oil or mixture thereof comprising the composition, and the amount of pan releasing agent in the composition,
The thinning agent is added to the cooking spray compositions in an amount sufficient to reduce the viscosity of the compositions to a desired viscosity. The thinning agent is added in an amount sufficient to produce a non-propellant cooking spray composition comprising a viscosity of about 25 centipoise (cPs) to about 45 cPs. Viscosity is determined with a Brookfield Viscometer, Model RVF (Brookfield Engineering, Middleboro, Mass.) at room temperature (e.g., 68-72° F.) with spindle #1 at 20 rpm. In some of the compositions, the viscosity comprises about 25 cPs to about 45 cPs, about 30 cPs to about 40 cPs, or about 32 cPs to about 36 cPs. In some of the compositions, the viscosity comprises about 30 cPs to about 38 cPs, about 30 cPs to about 37 cPs, about 30 cPs to about 36 cPs, about 30 cPs to about 35 cPs, about 30 cPs to about 34 cPs, about 30 cPs to about 33 cPs, or about 30 cPs to about 32 cPs. In some of the compositions, the viscosity comprises about 32 cPs to about 36 cPs, about 33 cPs to about 36 cPs, about 34 cPs to about 36 cPs, or about 35 cPs to about 36 cPs. In some of the compositions, the viscosity comprises about 36 cPs to about 37 cPs. In some of the compositions, the viscosity comprises about 30 cPs, about 30.5 cPs, about 31 cPs, about 31.5 cPs, about 32 cPs, about 32.5 cPs, about 33 cPs, about 33.5 cPs, about 34 cPs, about 34.5 cPs, about 35 cPs, about 35.5 cPs, about 36 cPs, about 36.5 cPs, or about 37 cPs. In some of the compositions, the viscosity comprises, about 25 cPs, about 26 cPs, about 27 cPs, about 28 cPs, about 29 cPs, about 30 cPs, about 21 cPs, about 32 cPs, about 33 cPs, about 34 cPs, about 35 cPs, about 36 cPs, about 37 cPs, about 38 cPs, about 39 cPs, about 40 cPs, about 41 cPs, about 42 cPs, about 43 cPs, about 44 cPs, or about 45 cPs.
The thinning agent comprises about 0% to about 15% by weight of the non-propellant cooking spray compositions. In some of the compositions, the thinning agent comprises about 5% to about 15%, about 6% to about 15%, about 7% to about 15%, about 8% to about 15%, about 9% to about 15%, about 10% to about 15%, about 11% to about 15%, or about 12% to about 15% by weight of the composition. In some of the compositions, the thinning agent comprises about 10% to about 13%, about 10.5% to about 13%, about 11% to about 13%, about 11.5% to about 13%, about 12% to 13%, or 12.5% to about 13% by weight of the composition. In some of the compositions, the thinning agent comprises about 12%, about 12.1%, about 12.2%, about 12.3%, about 12.4%, about 12.5%, about 12.6%, about 12.7%, about 12.8%, about 12.9%, or about 13% by weight of the composition.
The non-propellant cooking spray compositions optionally include one or more preservatives, flavorings, or colorants. One or more preservatives may be included in the compositions. The one or more preservatives are preferably FDA approved for food products. The preservative is preferably an antioxidant. Examples of suitable preservatives include, but are not limited to, propyl gallate, butylated hydroxyanisole, tertiary butylhydroxyquinone, tocopherol, and plant extracts comprising one or more natural antioxidants. Typically, the one or more preservatives comprises about 0.01% to about 0.1% by weight of the composition.
If a particular color is desired for the non-propellant cooking spray compositions, one or more colorants may be added. Preferably the colorants are FDA approved for food products. Examples of suitable colorants include, but are not limited to, annatto and beta-carotene. Typically, a small quantity of the colorants is required, with a range of about 5 to about 10 parts per million being sufficient.
If a particular flavor is desired for the non-propellant cooking spray compositions, one or more flavorings may be added. Preferably the flavorings are concentrated. The flavorings may be in liquid form or dry form. Examples of flavorings include, but are not limited to, butter flavor, garlic flavor, smoke flavor including but not limited to mesquite flavor and hickory flavor, and Italian herb flavor. Typically, the one or more flavorings comprises about 0.01% to about 2% by weight of the composition.
Methods for preparing the non-propellant cooking spray compositions described herein are also provided. The methods include adding lecithin heated to about 100° F. to about 140° F. to a mixing tank containing an edible oil or mixture of edible oils and mixing the oil and lecithin. The mixing tank contains a conventional motor-driven stirrer, such as a variable speed mixer or “Lightnin” type agitator. The MCT and the ethyl alcohol (if desired) is added to the oil and lecithin mixture while maintaining moderate non-aerating agitation and the composition is mixed until homogenous, the composition should be a uniform dispersion with no striations. To prevent separation, the agitation can be reduced from vigorous to a slow, continuous, non-aerating agitation until the composition is placed into the dispenser. Preparation of the compositions is generally carried out at ambient temperatures, generally about 68° F. to about 90° F. In some cases, depending on the particular formulation employed, continued or periodic mixing may be necessary to insure that all ingredients remain uniformly suspended and dispersed in the composition.
The following examples are provided for illustrative purposes only, and are in no way intended to limit the scope of the present application. All references in the Tables and Examples to “%” or “percent” mean percent by weight as defined above, unless specifically noted otherwise.
Non-propellant cooking spray compositions in accordance with the present application were prepared to illustrate the operability of the compositions. The compositions were produced as described above. Briefly, lecithin (50-54% by weight in vegetable oil—Kosher) was heated to about 100° F. to about 140° F. and added to a mixing tank containing canola oil. The mixing tank contained a variable speed mixer and a tight fitting lid to prevent absorption of moisture. The canola oil and lecithin were mixed using moderate, non-aerating agitation at ambient temperature. The MCT (NEOBEE® 895; Stepan Co., Northfield, Ill.) and ethyl alcohol (pure 200 proof ethyl alcohol) was added to the oil and lecithin mixture while maintaining moderate non-aerating agitation and the composition was mixed at ambient temperature until homogenous. To prevent separation, agitation was reduced from vigorous to a slow, continuous, non-aerating agitation until the composition was placed into the dispenser. Formulations of the non-propellant cooking spray compositions that were prepared are shown in Table 1.
Viscosity of the cooking spray compositions was determined with a Brookfield Viscometer, Model RVF (Brookfield Engineering, Middleboro, Mass.) at room temperature (e.g., 68-72° F.) with spindle #1 at 20 rpm.
As previously stated, the size of the orifice 102 of the nozzle 48 is a function of the fluid viscosity of the product. In the subject example, the size of the orifice 102 of the nozzle 48 is a function of the percentage by weight of thinning agent. As the amount of thinning agent is increased in the cooking spray composition, the viscosity decreases which allows for a smaller size orifice 102 for a given fluid pressure.
Although the subject matter has been described in language specific to structural features, compositions, and/or methodological acts, it is to be understood that the subject matter defined in the appended claims is not necessarily limited to the specific features, compositions, or acts described above. Rather, the specific features, compositions, and acts described above are disclosed as example forms of implementing the claims.
This application claims priority to U.S. Patent Application Ser. No. 60/990,548 filed on Nov. 27, 2007 and entitled “Spray Dispenser.”
Number | Name | Date | Kind |
---|---|---|---|
4142003 | Sejpal | Feb 1979 | A |
4155770 | Doumani | May 1979 | A |
4345718 | Horvath | Aug 1982 | A |
5088649 | Hanson et al. | Feb 1992 | A |
5296021 | Clapp et al. | Mar 1994 | A |
5455055 | Stoltz | Oct 1995 | A |
5638994 | Libit et al. | Jun 1997 | A |
6210743 | Clapp et al. | Apr 2001 | B1 |
6474510 | Frutin | Nov 2002 | B2 |
6799701 | Weiperth | Oct 2004 | B2 |
7455199 | Cockings et al. | Nov 2008 | B2 |
20040222246 | Bates et al. | Nov 2004 | A1 |
Number | Date | Country | |
---|---|---|---|
20090140011 A1 | Jun 2009 | US |
Number | Date | Country | |
---|---|---|---|
60990548 | Nov 2007 | US |