US20100147282A1 - Food Heating Device - Google Patents

Food Heating Device Download PDF

Info

Publication number
US20100147282A1
US20100147282A1 US12/085,887 US8588707A US2010147282A1 US 20100147282 A1 US20100147282 A1 US 20100147282A1 US 8588707 A US8588707 A US 8588707A US 2010147282 A1 US2010147282 A1 US 2010147282A1
Authority
US
United States
Prior art keywords
water
heat
food
amount
bag
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/085,887
Inventor
Yukio Urume
Hisao Kimura
Mikio Takaiwa
Yukako Kumagai
Yumiko Mine
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mycoal Co Ltd
Original Assignee
Mycoal Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mycoal Co Ltd filed Critical Mycoal Co Ltd
Assigned to MYCOAL CO., LTD. reassignment MYCOAL CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KIMURA, HISAO, KUMAGAI, YUKAKO, MINE, YUMIKO, TAKAIWA, MIKIO, URUME, YUKIO
Publication of US20100147282A1 publication Critical patent/US20100147282A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/16Materials undergoing chemical reactions when used
    • C09K5/18Non-reversible chemical reactions
    • AHUMAN NECESSITIES
    • A47FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
    • A47JKITCHEN EQUIPMENT; COFFEE MILLS; SPICE MILLS; APPARATUS FOR MAKING BEVERAGES
    • A47J36/00Parts, details or accessories of cooking-vessels
    • A47J36/24Warming devices
    • A47J36/28Warming devices generating the heat by exothermic reactions, e.g. heat released by the contact of unslaked lime with water
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D81/00Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
    • B65D81/34Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents for packaging foodstuffs or other articles intended to be cooked or heated within the package
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D81/00Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
    • B65D81/34Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents for packaging foodstuffs or other articles intended to be cooked or heated within the package
    • B65D81/3484Packages having self-contained heating means, e.g. heating generated by the reaction of two chemicals
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/16Materials undergoing chemical reactions when used

Definitions

  • the present invention relates to a food heating device to heat a food (cooked food such as a retort-packed food and canned drink) using a heat source activated by reaction with water. More particularly, it relates a food heating device improved in heat-generating property when temperature of water to be used is low.
  • a heat source activated by reaction with water As a heat source activated by reaction with water, a mixture of aluminum powder and calcium oxide powder has been popularly used for a heat-generating composition (referring to Patent literature 1, for example). And, a food heating device to heat a lunch bag or Japanese sake, or to re-heat a cooked food such as a retort-packed food in emergency situations, which uses the heat source, has been also known.
  • the calcium oxide powder is reacted with the water to generate heat and also calcium hydroxide produced by the reaction is reacted with the aluminum powder to generate heat.
  • the group of reactions makes it possible to generate enough amounts of heat to warm the food within a short period.
  • the above Japanese Patent shows that the disclosed heat-generating composition generates heat of about 100° C. after about 30 seconds from the reaction and the temperature is kept for 20 minutes or longer. And, the heat-generating composition has advantages in which it reacts without generating odor, and a small amount of the composition is enough for generating sufficient amounts of heat.
  • Patent literature 1 Japanese Patent number 3467729
  • the heat-generating composition is enclosed in an inner bag made by nonwoven fabric and further tightly enclosed in a watertight outer bag.
  • the enclosed heat-generating composition is taken out of the outer bag and comes in contact with water, resulting in that the heat-generating composition in the inner bag contacts the water to be reacted.
  • the water permeates the inner bag made by nonwoven fabric and reacts with the heat-generating composition in the inner bag.
  • the faster the water contacts the heat-generating composition the faster the heat-generating reaction proceeds.
  • the generated heat diffuses through the heated water and water vapor.
  • the higher the water permeability of the inner bag is, the faster the rate of the heat diffusion is.
  • Such a food heating device is sometimes used under a condition in which temperature of the water to be reacted is low. Therefore, such a food heating device is required which has excellent heat-generating abilities (rate of temperature rise, heat retaining period and the like) even under a condition in which temperature of the water to be reacted is low.
  • a food heating device comprises a heat source and a container having an exhaust vent, in which said heat source is put in said container together with a food to be heated and water is added to said container so that said heat source is reacted with said water to generate heat and to heat the food by the generated heat.
  • said heat source comprises: a bag formed by a packing material made of a base material of nonwoven fabric of which one surface is laminated with a waterproof layer, said packing material being punched with a plurality of pinholes, and a heat-generating composition containing aluminum powder in an amount of 40 to 60% by weight, calcium hydroxide powder in an amount of 10 to 40% by weight and calcium oxide powder in an amount of 10 to 40% by weight, enclosed in said bag, said packing material has a water permeable rate of 13 to milliliter/min/1 cm 2 measured under the following measurement conditions (1) to (4):
  • NaOH and KOH can not be used as an alkaline material because of the poisonous property.
  • substances which are easily dissociated by hydrolysis are also not suitable for heating a retort-packed rice and the like because the reaction terminates quickly. It means that an amount of heat which is discharged out of the food heating device is so large that the reaction can not proceed continuously.
  • calcium hydroxide as an alkaline material in view of cost and manufacturing method.
  • the proceeding of the heat-generating reaction can be controlled. That is, when a water permeable rate of the inner bag is set to 13 to 81 milliliter/min/1 cm 2 , preferably 13 to 65 milliliter/min/1 cm 2 , and more preferably 22 to 44 milliliter/min/1 cm 2 measured when head of water is 27 cm, preferable heating conditions including rate of temperature rise of a food, risen temperature and duration of the risen temperature under conditions in which a food heating device is typically used can be obtained. And, leakage of the heat-generating composition from the bag can be prevented.
  • the heat-generating composition contains calcium oxide powder in an amount of 10 to 40% by weight.
  • the calciumoxide (CaO) causes the following hydration reaction
  • the hydration reaction also generates heat and the produced Ca(OH) 2 reacts with aluminum to generate heat because it is an alkaline material. Accordingly, rate of temperature rise becomes fast.
  • the heat-generating composition contains aluminum powder in an amount of 40 to 60% by weight and calcium oxide powder in an amount of 10 to 40% by weight.
  • a heating device in which a heat-generating composition containing aluminum powder and calcium oxide (CaO) powder is reacted with water to generate heat has been widely known.
  • the present inventors have found that an addition of calcium hydroxide (Ca(OH) 2 ) to the above heat-generating composition allows an excellent heat-generating abilities even if temperature of water to be reacted is low.
  • a heat-generating composition it becomes possible to accomplish a request for-heating a food (retort-packed cooked curry or rice, 350-milliliter plastic bottled tea and the like) to 40° C. or higher after 5 minutes from the heat-generating reaction, to 60° C. or higher after 10 minutes and to keep the temperature after 20 minutes when temperature of water to be reacted is low as 5 to 30° C. (an environmental temperature is ⁇ 10 to 40° C.), for example.
  • nonwoven fabric examples include natural fabric such as cotton and wool; regenerated fiber such as viscose (rayon) and cupra; polyamide such as nylon 6, nylon6,6; straight-chain or branched polyesters having 20 or less carbon atoms such as polyethylene terephthalate, polytrimethylen terephthalate, polybutylene terephalate, polylactic acid and polyglycolic acid; polyolefins such as polyethylene and polypropylene; and synthetic fiber such as acrylic. Two or more kinds of those materials may be used together.
  • the nonwoven fabric may be made by a spunlaced method, spunbond method and the like.
  • Exemplary properties of the nonwoven fabric are followed: basis weight (g/m 2 );40 ⁇ 70,thickness ( ⁇ m);170 ⁇ 460, longitudinal tensile strength (N/5 cm); 35 ⁇ 380, transverse tensile strength(N/5 cm);13 ⁇ 165, longitudinal extensibility (%); 80 and below and transverse extensibility (%); 120 and below.
  • the watertight layer may be formed by laminating a synthetic-resin film on the nonwoven fabric.
  • exemplary synthetic-resin films include polyolefin resin such as polyethylene and polypropylene; polyamide resin; polyester resin; polyvinyl chloride resin; polystyrene resin; copolymer polyamide resin; copolymer polyester resin; ethylene-vinyl acetate resin; elastmer; and mixed resin of two or more of those resins.
  • the synthetic-resin film may be a single layer or laminated layer.
  • the synthetic-resin film has a thickness of 0.01 to 0.3 mm, preferably 0.02 to 0.1 mm
  • the heat-generating composition preferably has a weight of 30 g or more.
  • a weight ratio of the aluminum powder, the calcium hydroxide powder and the calcium oxide powder of the heat-generating composition is set to 40 ⁇ 60:10 ⁇ 40:10 ⁇ 40.
  • a weight ratio of the aluminum powder, the calcium hydroxide powder and the calcium oxide powder is preferably set to 40 ⁇ 50:15 ⁇ 40:20 ⁇ 40.
  • the aluminum powder preferably has following grain size distribution: ⁇ 45 ⁇ m; 70 ⁇ 95%, 45 ⁇ 63 ⁇ m; 5 ⁇ 20%, 63 ⁇ 75 ⁇ m; 0 ⁇ 5% and +75 ⁇ m; 0 ⁇ 5%.
  • the calcium hydroxide powder preferably has following grain size distribution: ⁇ 45 ⁇ m; 0 ⁇ 10%, 45 ⁇ 75 ⁇ m; 0 ⁇ 30%, 75 ⁇ 150 ⁇ m; 20 ⁇ 45% and +150 ⁇ m; 30 ⁇ 78%
  • the calcium oxide powder preferably has following grain size distribution: ⁇ 75 ⁇ m; 5 ⁇ 25%, 75 ⁇ 150 ⁇ m; 20 ⁇ 40% and +150 ⁇ m; 45 ⁇ 65% or ⁇ 75 ⁇ m; 25 ⁇ 90%, 75 ⁇ 150 ⁇ m; 5 ⁇ 70% and +150 ⁇ m; 0 ⁇ 15%.
  • Examples of the food to be heated include a food such as a retort-packed food, canned drink, boiled egg and lunch bag.
  • the container may have any forms including a bag, box andpan.
  • the exhaust vent is for discharging H 2 and H 2 O produced by the aforesaid heat-generating reaction.
  • a size and number of the vent is selected such that expansion and breakage of the container can be prevented while keeping heat-retaining property.
  • a food heating device utilizing a heat source having preferable heating conditions including rate of temperature rise of the food, risen temperature of the food and duration of the risen temperature under conditions in which a food heating device is typically used, can be provided.
  • a food heating device can be provided which has excellent heat-generating abilities even if temperature of the water to be reacted is low.
  • the present invention shows that heat-generating ability of the heat source can be controlled by water permeability of the inner bag as well as the property of the heat-generating composition.
  • a non water-repellent nonwoven fabric made by 100% rayon, MR-50/PP40, manufactured by Kokko Paper Mfg. Co., Ltd.
  • the nonwoven fabric has the following properties: basis weight (g/m 2 ) ; 50, thickness ( ⁇ m) ; 400, longitudinal tensile strength (N/25 cm) ; 41, transverse tensile strength (N/25 cm); 9.5, longitudinal extensibility (%) ; 27 and below and transverse extensibility (%); 120 and below.
  • the nonwoven fabric is made by a spunlaced method in which columnar water flow injects toward fibers at high pressure to entwine the fibers and thus to produce a nonwoven fabric.
  • the spunlaced method allows a production of a highly flexible napless nonwoven fabric having high drape property.
  • a nonwoven fabric produced by the method is used for livelihood materials such as diaper, medical supplies, food supplies and cleaning supplies.
  • a water-resistant layer (made by polypropylene) was laminated.
  • the water-resistant layer may be made by a heating bonding and the like in exchange for the laminating.
  • the water-resistant layer had a thickness of 40 ⁇ m.
  • Each of the prepared base materials was punched with pinholes in various densities using a pinhole opening machine, which comprised a roller on which needles were arranged at intervals of 3. 0mm in the transverse direction and at intervals of about 2.9 mm in the longitudinal direction and a base material supporting roller confronting to the former roller.
  • a pinhole opening machine which comprised a roller on which needles were arranged at intervals of 3. 0mm in the transverse direction and at intervals of about 2.9 mm in the longitudinal direction and a base material supporting roller confronting to the former roller.
  • another type of the pinhole opening machine may be used, which is provided with needles capable of being heated and the heated needles are made to contact the laminated film to fuse the film, resulting in opening pinholes.
  • the pinhole diameter varied over a range of 0.05 to 0.4 mm.
  • the pinhole density was 1150/100 cm 2 . If the diameter of the pinhole is larger, the small particulate heat-generating composition may be leaked through the pinhole from the bag, causing unfavorable situation. Accordingly, the pinhole diameter should be small (0.05 to 0.4 mm) within the scope showing excellent heat-generating property.
  • Each of the base materials was cut into a piece having a size of 50 mm by 50 mm to prepare a sample for measuring water permeability.
  • FIG. 3 is a drawing showing the water permeable rate measuring method in the present invention.
  • a stainless-steel measuring tank 51 (inside dimension of 335 ⁇ 535 ⁇ 178 mm) was prepared and filled with ion-exchange water of 23 ⁇ 3° C.
  • An in flow pipe 53 from which the ion-exchange water flowed in the tank 51 was formed at the under portion of the side wall of the tank 51 and an overflow pipe 55 was formed at the upper portion of the side wall of the tank 51 .
  • the pipes 53 and 55 were openable and closable by cocks 54 and 56 , respectively.
  • the ion-exchange water was poured into the tank 51 from the inflow pipe 53 and overflowed through the overflow pipe 55 .
  • An outflow pipe 57 (diameter of 19.05 mm) extending downward was formed on the bottom of the tank 51 .
  • the outflow pipe 57 was openable and closable by a cock 58 .
  • the sample base materials S was temporarily attached to the opening of the outflow pipe 57 by a rubber band 59 with the watertight surface of the sample S being upside. Then, the periphery of the sample was closely attached to the pipe by a sealing tape to block the opening with the sample S and then further tightly attached by a water impermeable adhesive tape made by polypropylene.
  • a distance H between the opening of the outflow pipe 57 and the overflow port of the overflow pipe 55 was 270 ⁇ 9.5 mm (head of water).
  • a collection vessel 61 was disposed under the opening of the outflow pipe 57 .
  • the collection vessel 61 was set on a measurement apparatus (not shown, GF-3000, manufactured by A&D Co., Ltd.).
  • the tank 51 was kept the overflow state with the both cocks 54 and 56 opened.
  • the cock 58 of the outflow pipe 57 was opened, the water was collected by the vessel 61 . And, the amount (milliliter) of the collected water was weighed. In this case, after an amount of the permeated water per unit time had got constant (after a variation in amount of the permeated water per 10 seconds was within 5% at least consecutive three times), an amount of the permeated water measured in any one minute during the measurement for one minute or more was defined as a water permeable amount (milliliter). And, a water permeable amount per one minuet per 1 cm 2 of the sample was converted to water permeable rate (milliliter/min/cm 2 ). A specific gravity of the ion-exchange water is set to 1.000 (g/cm 3 ).
  • the air permeability was measured using a gurley type densometer (range; 300 ml, timer;s, t ⁇ 1, a diameter of measuring section; 30 mm, manufactured by Toyo Seiki Seisaku-Sho, Ltd., based on JIS P8117).
  • the measured value (sec/300 ml) was converted to an air permeable rate (milliliter/min/cm 2 ).
  • the prepared six samples having various pinhole diameters were examined for water permeability using the aforesaid measuring apparatus and also for air permeability using the gurley type densometer.
  • Table 1 shows the measured air permeability, air permeable rate converted from the measured air permeability, the measured water permeability and water permeable rate converted from the measured water permeability.
  • FIG. 4 is a graph showing a relation between the air permeable rate and the water permeable rate.
  • the vertical axis indicates the water permeable rate converted from the measured water permeability
  • the horizontal axis indicates the air permeable rate converted from the air permeability measured by the gurley type densometer.
  • the water permeable rate can be expressed by a direct function of the air permeable rate. From the direct function, a ratio of the water permeable rate to the air permeable rate is substantially equal to 1/5.5 in a case of the packing material of the present invention.
  • a heat source was produced using each of the prepared bags. And, a relation between the temperature of the heat source and the air permeability of the bags was examined.
  • the heat-generating composition As the heat-generating composition, a mixed powder of aluminum powder (#280A, manufactured by MINALCO Co., Ltd.) of 20 g, calcium hydroxide powder (tokusen, manufactured by Tage lime industry) of 10 g and calcium oxide powder (manufactured by Tage lime industry) of 20 g and was used.
  • the aluminum powder has the following grain size distribution: -45 ⁇ m; 90.80%, 45 ⁇ 63 ⁇ m; 8.30%, 63 ⁇ 75 ⁇ m; 0.64% and +75 ⁇ m; 0.25%.
  • the calcium hydroxide powder has the following grain size distribution: ⁇ 45 ⁇ m; 4.60%, 45 ⁇ 75 ⁇ m; 21.90%; 75 ⁇ 150 ⁇ m; 35.92% and +150 ⁇ m; 37.58%.
  • the calcium oxide powder has the following grain size distribution: ⁇ 75 ⁇ m; 15.68%, 75 ⁇ 150 ⁇ m; 34.24% and +150 ⁇ m; 50.07%.
  • the calcium oxide powder includes the following elements: calcium oxide (measured by an EDTA titration method (NN indicator)); 93% or more, carbon dioxide (measured by a Storelain method); 2.0% and below and impurities (measured by an EDTA titration method, perchloric acid method, absorption spectroscopy); 3.2% or less.
  • the impurities include silicon dioxide, aluminum oxide, ferric oxide and magnesium oxide.
  • the bag having a receptacle for containing the heat-generating composition was produced.
  • the receptacle had a size of 70 mm ⁇ 170 mm.
  • FIG. 5 is a drawing showing the method for measuring the temperature.
  • the heat source 1 a food F (a retort-packed cooked rice and a 350 millilitter-plastic bottled tea, or a retort-packed cooked rice and a retort-packed curry) and water of 130 g were put in a heating bag 31 having exhaust vents 32 .
  • the heating bag 31 was openable and closable and had two exhaust vents 32 having a diameter of 5 mm.
  • the heating bag 31 was supported in a stainless-steel container 73 set on a heat insulating material 71 .
  • a temperature T 1 in the heating bag 31 steam temperature
  • a temperature T 2 of the heated water an environmental temperature T 3 and a temperature T 4 of the food were measured by the measuring apparatus D.
  • Table 2 shows a result whether the samples satisfied the heating conditions.
  • condition B condition C 40° C. or higher 50° C. or higher 60° C. or higher after 5 min. after 5 min. after 5 min. after 5 min. 60° C. or higher 60° C. or higher 65° C. or higher after 10 min. and after 10 min. and after 10 min. and after 10 min. and after 10 min. and and Sample 60° C. or higher 65° C. or higher 65° C. or higher No. after 20 min. after 20 min. after 15 min. 1 ⁇ x x 2 ⁇ ⁇ ⁇ 3 ⁇ ⁇ ⁇ 4 ⁇ ⁇ ⁇ 5 ⁇ x x 6 x x x x x x
  • Temperature of the heat source can be controlled by the air permeable rate of the bag.
  • the air permeable rate of the bag required for heating a food is 110 to 340 milliliter/min/cm 2 (water permeable rate is about 24 to 44 milliliter/min/cm 2 ).
  • a preferable water permeable rate of the bag for heating a food is 13 to 81 milliliter/min/cm 2 .
  • the heat-generation of the heat-generating composition is caused by a heat-generating reaction of the aluminum after a formation of alkaline environment resulting from hydrolysis of the calcium hydroxide, as described above, and also by a heat-generating reaction of the aluminum activated by a heat-generating resulting from a hydration reaction of the calcium oxide.
  • a low-temperature (low-water temperature) condition either one of the heat-generating reactions alone will not generate sufficient amount of heat.
  • rate of temperature rise becomes better.
  • Ca(OH) 2 produced by a hydration reaction of CaO does not have so high water-solubility because the water temperature rises rapidly to 70 to 80° C. due to heat generated by the aforesaid hydration reaction. Accordingly, although hydrolysis rate is rapid, it requires a longer time until the pH sifts toward alkalis.
  • Each of the sample heat-generating compositions was enclosed with the bag made of base material (a non water-repellent nonwoven fabric (made by 100% rayon, MR-50/PP40,manufactured by Kokko Paper Mfg. Co., Ltd.) having a water permeable rate of about 40 to 44 milliliter/min/cm 2 ) used for measurement of the water permeability.
  • base material a non water-repellent nonwoven fabric (made by 100% rayon, MR-50/PP40,manufactured by Kokko Paper Mfg. Co., Ltd.) having a water permeable rate of about 40 to 44 milliliter/min/cm 2 ) used for measurement of the water permeability.
  • base material a non water-repellent nonwoven fabric (made by 100% rayon, MR-50/PP40,manufactured by Kokko Paper Mfg. Co., Ltd.) having a water permeable rate of about 40 to 44 milliliter/min/cm 2 ) used for measurement of
  • a retort-packed rice was measured in temperature in such a manner that a stick type temperature sensor was inserted into the center of the retort-packed rice. Then, whether the samples satisfied the heating condition D (to heat the retort-packed rice to 60° C. or higher after 25 minutes) and condition E (to heat the retort-packed rice to 65° C. after 25 minutes) was discussed.
  • Table 3 shows results whether the samples satisfied the heating conditions.
  • the food heating condition D (to heat the retort-packed rice to 60° C. or higher after 25 minutes) is satisfied when the aluminum powder, calcium hydroxide powder and calcium oxide powder has an amount ratio of 40 ⁇ 60:10 ⁇ 40:10 ⁇ 40.
  • the food heating condition E (to heat the retort-packed rice to 65° C. or higher after 25 minutes) is satisfied when the aluminum powder, calcium hydroxide powder and calcium oxide powder has an amount ratio of 50 ⁇ 60:10 ⁇ 20:20 ⁇ 35.
  • a weight of the heat-generating composition Concerning a weight of the heat-generating composition, the following measurement was carried out.
  • the heat-generating composition containing the aluminum powder, calcium hydroxide powder and calcium oxide powder with an amount ratio of the aluminum powder, calcium hydroxide powder and calcium oxide powder being 50:15:35 was enclosed in the bag to prepare the heat sources each having a weight of 30 g, 40 g, 50 g and 60 g.
  • Each of the heat sources was examined in temperature measurement. As a result, all of the heat sources showed substantially the same heat-generating ability. Therefore, a weight of the heat-generating composition is preferably 30 g or larger.
  • FIG. 1 is a drawing showing a structure of a heat source according to the present invention
  • FIG. 1A is a plane drawing
  • FIG. 1B is a cross-section drawing.
  • the heat source 1 comprises a bag 10 and a heat-generating composition 20 enclosed in the bag 10 .
  • the bag 10 is made of a non water-repellent nonwoven fabric 11 (100% rayon, MR-50/PP40, manufacturedbyKokko Paper Mfg. Co., Ltd.). Almost full area of the bag 10 is punched with pinholes 15 in substantially the uniform density.
  • the pinhole 15 has a diameter of 0.1 to 0.3 mm.
  • the bag 10 has a water permeable rate, measured by the aforesaid method (as shown in FIG. 3 ), of about 40 milliliter/min/cm 2 .
  • the water permeable rate can be converted from the air permeable rate measured by the gurley type densometer.
  • the bag 10 has a size of 70 mm ⁇ 170 mm.
  • the heat-generating composition 30 is a mixed powder of aluminum powder (#280A, manufactured by MINALCO Co., Ltd.) of 25 g, calcium hydroxide powder (tokusen, manufactured by Tage lime industry) of 7.5 g and calcium oxide powder (manufactured by Tage lime industry) of 17.5 g (an amount ratio of aluminum:calciumhydroxide:calciumoxide is 50:15:35. A total weight is 50 g).
  • the heat-generating composition 20 is enclosed in the bag 10 to produce the heat source 1.
  • Example 2 The same heat-generating composition as that of Example (an amount ratio of aluminum:calcium hydroxide:calcium oxide is 50:15:35. A total weight is 50 g) was enclosed in the bag 10 having a water permeable rate of about 81 milliliter/min/cm 2 to produce another heat source 3 .
  • FIG. 2 is a drawing showing a heating device according to the present invention.
  • the heating device is used for heating a retort-packed cooked rice and a retort-packed cooked curry.
  • the food heating device 30 comprises a heating bag (container) 31 having exhaust vents 32 ; the heat source 1 shown in FIG. 1 and water W for activating a heat-generating reaction.
  • a heating bag (container) 31 having exhaust vents 32 In this embodiment, two circular exhaust vents 32 having a diameter of 5 mm are formed. Or, two to four exhaust vents 32 having a diameter of 3 to 7 mm may be formed. Depending on the container, one to two exhaust vents having a diameter of 10 to 15 mm, or eight to ten exhaust vents having a diameter of 1 to 2 mm may be formed.
  • the shape of the exhaust vent is not limited to a circular shape; may be any shape capable of venting water vapor and hydrogen gas. When the bag is a three sided seal pack, the exhaust vent may have a shape formed by turning the opening of the back.
  • the heat source 1 is enclosed in an air-tight outer bag during storing in order to prevent the heat-generating composition from contacting moisture in air.
  • the heat source 1 taken out of the outer bag, the retort-packed cooked rice and the retort-packed cooked curry D were put in the heating bag (container) 31 , water of about 5° C. in an amount of 130 g was added and then the container 31 was sealed.
  • the heat source 1 caused a heat-generating reaction to heat the retort-packed cooked rice and retort-packed cooked curry Din the container 31 .
  • Water vapor and hydrogen gas produced by the heat-generating reaction were vent through the exhaust vents 32 .
  • the retort-packed cocked rice was heated to 67.3° C. And, leakage of the heat-generating composition did not occur.
  • the heat source 3 was used in exchange for the heat source 1 .
  • the heat source 3 taken out of the outer bag, and 350 milliliter-plastic bottled tea D were put in the heating bag (container) 31 , water of about 20° C. in an amount of 130 g was added and then the container 31 was sealed.
  • the heat source 3 taken out of the outer bag, and a retort-packed cooked rice D were put in the heating bag (container) 31 , water of about 5° C. in an amount of 130 g was added and then the container 31 was sealed.
  • FIG. 6 is a graph showing a relation between the measurement time and temperatures.
  • non water repellent nonwoven fabric In exchange for the aforesaid non water-repellant nonwoven fabric, another type of non water repellent nonwoven fabric maybe used, for example, CO40s (manufactured by Unitika Co., Ltd.), which has the following properties: basis weight (g/m 2 ); 40, thickness ( ⁇ m); 330, longitudinal tensile strength (N/5 mm); 35, transverse tensile strength (N/5 mm); 15, longitudinal extensibility (%); 25 and transverse extensibility (%); 75.
  • the nonwoven fabric was made by a spunlaced method.
  • a weight ratio of the aluminum power, calcium hydroxide powder and calcium oxide powder, weight of the heat-generating composition and properties are not limited to the aforesaid values.
  • FIG. 1 is a drawing showing a structure of a heat source according to the present invention
  • FIG. 1A is a plane drawing
  • FIG. 1B is a cross-section drawing.
  • FIG. 2 is a drawing showing a heating device according to the present invention.
  • FIG. 3 is a drawing showing the water permeable rate measuring method in the present invention.
  • FIG. 4 is a graph showing a relation between the air permeable rate and the water permeable rate.
  • FIG. 5 is a drawing showing the method for measuring the temperature.
  • FIG. 6 is a graph showing a relation between the measurement time and temperatures.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Food Science & Technology (AREA)
  • Thermal Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Combustion & Propulsion (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Cookers (AREA)
  • Package Specialized In Special Use (AREA)
  • Packages (AREA)

Abstract

The heat source 1 comprises a bag 10 and a heat-generating composition 20 containing aluminum powder, calcium hydroxide powder and calcium oxide powder, enclosed in the bag 10. The bag 10 is formed by a packing material made of a base material of nonwoven fabric of which one surface is laminated with a watertight layer. The packing material is punched with a plurality of pinholes and has a water permeable rate of 13 to 81 milliliter/min/1 cm2 measured when head of water is 27 cm. The heat source 1 can satisfy preferable heating conditions including rate of temperature rise of the food, risen temperature of the food, duration of the risen temperature of the food under conditions in which a food heating device is conventionally used. Accordingly, a food heating device using the heat source capable of causing a rapid and stable heat-generating reaction can be provided.

Description

    TECHNICAL FIELD
  • The present invention relates to a food heating device to heat a food (cooked food such as a retort-packed food and canned drink) using a heat source activated by reaction with water. More particularly, it relates a food heating device improved in heat-generating property when temperature of water to be used is low.
  • BACKGROUND ART
  • As a heat source activated by reaction with water, a mixture of aluminum powder and calcium oxide powder has been popularly used for a heat-generating composition (referring to Patent literature 1, for example). And, a food heating device to heat a lunch bag or Japanese sake, or to re-heat a cooked food such as a retort-packed food in emergency situations, which uses the heat source, has been also known.
  • In such the heat-generating composition, the calcium oxide powder is reacted with the water to generate heat and also calcium hydroxide produced by the reaction is reacted with the aluminum powder to generate heat. The group of reactions makes it possible to generate enough amounts of heat to warm the food within a short period. The above Japanese Patent shows that the disclosed heat-generating composition generates heat of about 100° C. after about 30 seconds from the reaction and the temperature is kept for 20 minutes or longer. And, the heat-generating composition has advantages in which it reacts without generating odor, and a small amount of the composition is enough for generating sufficient amounts of heat.
  • Patent literature 1: Japanese Patent number 3467729
  • DISCLOSURE OF THE INVENTION Problems to be solved by the Invention
  • In the aforesaid food heating device, the heat-generating composition is enclosed in an inner bag made by nonwoven fabric and further tightly enclosed in a watertight outer bag. When to be used, the enclosed heat-generating composition is taken out of the outer bag and comes in contact with water, resulting in that the heat-generating composition in the inner bag contacts the water to be reacted. The water permeates the inner bag made by nonwoven fabric and reacts with the heat-generating composition in the inner bag. In this case, it is considered that the faster the water contacts the heat-generating composition, the faster the heat-generating reaction proceeds. The generated heat diffuses through the heated water and water vapor. And, it is also considered that the higher the water permeability of the inner bag is, the faster the rate of the heat diffusion is. Accordingly, it is considered that an efficiency of the water permeation of the inner bag (water permeability) influences the proceeding of the heat-generating reaction of the heat-generating composition. However, in such food heating devices, development and proposal concerning to the water permeability of the inner bag have not been done.
  • Such a food heating device is sometimes used under a condition in which temperature of the water to be reacted is low. Therefore, such a food heating device is required which has excellent heat-generating abilities (rate of temperature rise, heat retaining period and the like) even under a condition in which temperature of the water to be reacted is low.
  • In view of this regard, the present invention focuses attention on the permeability of the inner bag and the object of the present invention is to provide a food heating device utilizing a heat source capable of a rapid and stable heat-generating reaction. Another object of the present invention is to provide a food heating device having a heat source providing excellent heat-generating abilities even when it reacts with low-temperature water.
  • Means of Solving the Problems
  • A food heating device according to the present invention comprises a heat source and a container having an exhaust vent, in which said heat source is put in said container together with a food to be heated and water is added to said container so that said heat source is reacted with said water to generate heat and to heat the food by the generated heat. And, said heat source comprises: a bag formed by a packing material made of a base material of nonwoven fabric of which one surface is laminated with a waterproof layer, said packing material being punched with a plurality of pinholes, and a heat-generating composition containing aluminum powder in an amount of 40 to 60% by weight, calcium hydroxide powder in an amount of 10 to 40% by weight and calcium oxide powder in an amount of 10 to 40% by weight, enclosed in said bag, said packing material has a water permeable rate of 13 to milliliter/min/1 cm2 measured under the following measurement conditions (1) to (4):
    • (1) ion-exchanged water of 23±3° C. is used,
    • (2) head of water is 27±0.95 cm,
    • (3) a water permeable area of said packing material is 2.85 cm2, and
    • (4) the water permeable amount (milliliter) is defined in such a manner that after an amount of the permeated water per unit time gets constant (after a variation in amount of the permeated water per 10 seconds is within 5% at least consecutive three times), an amount of the permeated water measured in any one minute during the measurement for one minute or more is converted into a water permeable amount (milliliter) using a specific gravity of the ion-exchange water of 1.000 (g/cm3).
  • On reacting with water, calcium hydroxide (Ca(OH)2) is hydrolyzed to exhibit strong alkaline. It is known that water-solubility of calcium hydroxide becomes high as the temperature of the water is low (for example, 0.189 wt % at 0° C. and 0.106 wt % at 80° C.). On the other hand, while aluminum does not react with water at room temperatures, it reacts with water under alkaline environment to cause the following decomposition reaction of water:

  • 2Al+2OH+6H2O→2Al(OH)4 +3H2.
  • When calcium hydroxide (Ca(OH)2) is used as an alkaline material, the above reaction formula is as follows:

  • 2Al+Ca(OH)2+6H2O→Ca2++2Al(OH)4 +3H2.
  • Since Ca2+ and 2Al(OH)4 , shown in the right-side hand in this formula, does not exhibit alkaline as strong as NaOH and KOH and an amount of dissociated Ca2+ and 2Al(OH)4 is significantly small, both ions are combined into CaO.Al2O3.4H2O. However, since the reaction proceeds in alkaline aqueous solution, the following reaction occurs:

  • 2Al+Ca(OH)2+2H2O→-CaO.Al2O3+3H2+183.7 Kcal
  • Therefore, in order to sift the chemical equilibrium toward the right-side hand, that is, to produce a heat-generating reaction, it is necessary that the dissolved Ca(OH)2 be hydrolyzed to shift the pH toward alkaline and to increase the dissolution rate of the aluminum.
  • Accordingly, by adding calcium hydroxide powder, which has a higher water-solubility under low-temperature environments, to the mixed powder previously, an excellent heat-generating ability can be provided even if temperature of the water to be reacted is low.
  • For heating a food, NaOH and KOH can not be used as an alkaline material because of the poisonous property. Or, substances which are easily dissociated by hydrolysis are also not suitable for heating a retort-packed rice and the like because the reaction terminates quickly. It means that an amount of heat which is discharged out of the food heating device is so large that the reaction can not proceed continuously.
  • Accordingly, it is preferable to use calcium hydroxide as an alkaline material in view of cost and manufacturing method.
  • According to the present invention, by controlling water permeable rate of the bag, the proceeding of the heat-generating reaction can be controlled. That is, when a water permeable rate of the inner bag is set to 13 to 81 milliliter/min/1 cm2, preferably 13 to 65 milliliter/min/1 cm2, and more preferably 22 to 44 milliliter/min/1 cm2 measured when head of water is 27 cm, preferable heating conditions including rate of temperature rise of a food, risen temperature and duration of the risen temperature under conditions in which a food heating device is typically used can be obtained. And, leakage of the heat-generating composition from the bag can be prevented.
  • In the present invention, the heat-generating composition contains calcium oxide powder in an amount of 10 to 40% by weight.
  • In this case, the calciumoxide (CaO) causes the following hydration reaction;

  • CaO+H2O→Ca(OH)2+15.6 Kcal.
  • The hydration reaction also generates heat and the produced Ca(OH)2 reacts with aluminum to generate heat because it is an alkaline material. Accordingly, rate of temperature rise becomes fast.
  • In the present invention, the heat-generating composition contains aluminum powder in an amount of 40 to 60% by weight and calcium oxide powder in an amount of 10 to 40% by weight.
  • A heating device in which a heat-generating composition containing aluminum powder and calcium oxide (CaO) powder is reacted with water to generate heat has been widely known. The present inventors have found that an addition of calcium hydroxide (Ca(OH)2) to the above heat-generating composition allows an excellent heat-generating abilities even if temperature of water to be reacted is low. By using such a heat-generating composition, it becomes possible to accomplish a request for-heating a food (retort-packed cooked curry or rice, 350-milliliter plastic bottled tea and the like) to 40° C. or higher after 5 minutes from the heat-generating reaction, to 60° C. or higher after 10 minutes and to keep the temperature after 20 minutes when temperature of water to be reacted is low as 5 to 30° C. (an environmental temperature is −10 to 40° C.), for example.
  • Examples of the heat-generating composition and nonwoven fabric for use in the prevent invention are described below.
  • Examples of the nonwoven fabric include natural fabric such as cotton and wool; regenerated fiber such as viscose (rayon) and cupra; polyamide such as nylon 6, nylon6,6; straight-chain or branched polyesters having 20 or less carbon atoms such as polyethylene terephthalate, polytrimethylen terephthalate, polybutylene terephalate, polylactic acid and polyglycolic acid; polyolefins such as polyethylene and polypropylene; and synthetic fiber such as acrylic. Two or more kinds of those materials may be used together. The nonwoven fabric may be made by a spunlaced method, spunbond method and the like.
  • Exemplary properties of the nonwoven fabric are followed: basis weight (g/m2);40˜70,thickness (μm);170˜460, longitudinal tensile strength (N/5 cm); 35˜380, transverse tensile strength(N/5 cm);13˜165, longitudinal extensibility (%); 80 and below and transverse extensibility (%); 120 and below.
  • The watertight layer may be formed by laminating a synthetic-resin film on the nonwoven fabric. Exemplary synthetic-resin films include polyolefin resin such as polyethylene and polypropylene; polyamide resin; polyester resin; polyvinyl chloride resin; polystyrene resin; copolymer polyamide resin; copolymer polyester resin; ethylene-vinyl acetate resin; elastmer; and mixed resin of two or more of those resins. The synthetic-resin film may be a single layer or laminated layer. The synthetic-resin film has a thickness of 0.01 to 0.3 mm, preferably 0.02 to 0.1 mm
  • In order to heat a retort-packed cooked rice or curry and plastic bottled tea, the heat-generating composition preferably has a weight of 30 g or more. A weight ratio of the aluminum powder, the calcium hydroxide powder and the calcium oxide powder of the heat-generating composition is set to 40˜60:10˜40:10˜40. Especially, in view of rate of temperature rise and duration of the risen temperature, a weight ratio of the aluminum powder, the calcium hydroxide powder and the calcium oxide powder is preferably set to 40˜50:15˜40:20˜40.
  • The aluminum powder preferably has following grain size distribution: ˜45 μm; 70˜95%, 45˜63 μm; 5˜20%, 63˜75 μm; 0˜5% and +75 μm; 0˜5%.
  • The calcium hydroxide powder preferably has following grain size distribution: ˜45 μm; 0˜10%, 45˜75 μm; 0˜30%, 75˜150 μm; 20˜45% and +150 μm; 30˜78%
  • The calcium oxide powder preferably has following grain size distribution: ˜75 μm; 5˜25%, 75˜150 μm; 20˜40% and +150 μm; 45˜65% or ˜75 μm; 25˜90%, 75˜150 μm; 5 ˜70% and +150 μm; 0˜15%.
  • Examples of the food to be heated include a food such as a retort-packed food, canned drink, boiled egg and lunch bag.
  • The container may have any forms including a bag, box andpan. The exhaust vent is for discharging H2 and H2O produced by the aforesaid heat-generating reaction. A size and number of the vent is selected such that expansion and breakage of the container can be prevented while keeping heat-retaining property.
  • Advantageous Effect of the Invention
  • As described above, according to the present invention, a food heating device utilizing a heat source, having preferable heating conditions including rate of temperature rise of the food, risen temperature of the food and duration of the risen temperature under conditions in which a food heating device is typically used, can be provided. Especially, a food heating device can be provided which has excellent heat-generating abilities even if temperature of the water to be reacted is low. And, the present invention shows that heat-generating ability of the heat source can be controlled by water permeability of the inner bag as well as the property of the heat-generating composition.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • Hereinafter, preferred embodiments of the present invention will be precisely described, referring to the drawings.
  • First, water permeability of an inner bag will be described.
  • <Water Permeability>
  • Sample bags made by various base materials which were punched with pinholes in various densities were prepared. And, water permeability (water permeable rate) of each sample was measured.
  • (1) Base Material
  • As the base material, a non water-repellent nonwoven fabric (made by 100% rayon, MR-50/PP40, manufactured by Kokko Paper Mfg. Co., Ltd.) was used. The nonwoven fabric has the following properties: basis weight (g/m2) ; 50, thickness (μm) ; 400, longitudinal tensile strength (N/25 cm) ; 41, transverse tensile strength (N/25 cm); 9.5, longitudinal extensibility (%) ; 27 and below and transverse extensibility (%); 120 and below. The nonwoven fabric is made by a spunlaced method in which columnar water flow injects toward fibers at high pressure to entwine the fibers and thus to produce a nonwoven fabric. The spunlaced method allows a production of a highly flexible napless nonwoven fabric having high drape property. A nonwoven fabric produced by the method is used for livelihood materials such as diaper, medical supplies, food supplies and cleaning supplies. On one surface of the nonwoven fabric, a water-resistant layer (made by polypropylene) was laminated. Or, the water-resistant layer may be made by a heating bonding and the like in exchange for the laminating. The water-resistant layer had a thickness of 40 μm.
  • (2) Pinholes
  • Each of the prepared base materials was punched with pinholes in various densities using a pinhole opening machine, which comprised a roller on which needles were arranged at intervals of 3. 0mm in the transverse direction and at intervals of about 2.9 mm in the longitudinal direction and a base material supporting roller confronting to the former roller. Or, another type of the pinhole opening machine may be used, which is provided with needles capable of being heated and the heated needles are made to contact the laminated film to fuse the film, resulting in opening pinholes. After the base material was supported to the base material supporting roller, each of the rollers rotated in opposite directions. As the result, pinholes were formed on the base material in substantially the uniform density over the almost full area. By changing a contact depth of the rollers, six base materials having various pinhole diameters were prepared. The pinhole diameters varied over a range of 0.05 to 0.4 mm. The pinhole density was 1150/100 cm2. If the diameter of the pinhole is larger, the small particulate heat-generating composition may be leaked through the pinhole from the bag, causing unfavorable situation. Accordingly, the pinhole diameter should be small (0.05 to 0.4 mm) within the scope showing excellent heat-generating property.
  • Each of the base materials was cut into a piece having a size of 50 mm by 50 mm to prepare a sample for measuring water permeability.
  • (3) Water Permeability
  • There is no official standard showing water permeability of fabric and the like. According to a method for measuring water permeable rate of perforated film, water permeability of each sample was examined by a water permeable rate measuring method, described later.
  • FIG. 3 is a drawing showing the water permeable rate measuring method in the present invention.
  • A stainless-steel measuring tank 51 (inside dimension of 335×535×178 mm) was prepared and filled with ion-exchange water of 23±3° C. An in flow pipe 53 from which the ion-exchange water flowed in the tank 51 was formed at the under portion of the side wall of the tank 51 and an overflow pipe 55 was formed at the upper portion of the side wall of the tank 51. The pipes 53 and 55 were openable and closable by cocks 54 and 56, respectively. The ion-exchange water was poured into the tank 51 from the inflow pipe 53 and overflowed through the overflow pipe 55.
  • An outflow pipe 57 (diameter of 19.05 mm) extending downward was formed on the bottom of the tank 51. The outflow pipe 57 was openable and closable by a cock 58. The sample base materials S was temporarily attached to the opening of the outflow pipe 57 by a rubber band 59 with the watertight surface of the sample S being upside. Then, the periphery of the sample was closely attached to the pipe by a sealing tape to block the opening with the sample S and then further tightly attached by a water impermeable adhesive tape made by polypropylene. A distance H between the opening of the outflow pipe 57 and the overflow port of the overflow pipe 55 was 270±9.5 mm (head of water). Under the opening of the outflow pipe 57, a collection vessel 61 was disposed. The collection vessel 61 was set on a measurement apparatus (not shown, GF-3000, manufactured by A&D Co., Ltd.).
  • The tank 51 was kept the overflow state with the both cocks 54 and 56 opened. When the cock 58 of the outflow pipe 57 was opened, the water was collected by the vessel 61. And, the amount (milliliter) of the collected water was weighed. In this case, after an amount of the permeated water per unit time had got constant (after a variation in amount of the permeated water per 10 seconds was within 5% at least consecutive three times), an amount of the permeated water measured in any one minute during the measurement for one minute or more was defined as a water permeable amount (milliliter). And, a water permeable amount per one minuet per 1 cm2 of the sample was converted to water permeable rate (milliliter/min/cm2). A specific gravity of the ion-exchange water is set to 1.000 (g/cm3).
  • Then, a relation between the measured water permeable rate and publicly known air permeability was examined. Because, the measurement of the water permeable rate needs troublesome handling, and, therefore if the water permeable rate is correlated with the air permeability, the measurement of the air permeability can be employed in exchange for the measurement of the water permeable rate.
  • The air permeability was measured using a gurley type densometer (range; 300 ml, timer;s, t<1, a diameter of measuring section; 30 mm, manufactured by Toyo Seiki Seisaku-Sho, Ltd., based on JIS P8117). The measured value (sec/300 ml) was converted to an air permeable rate (milliliter/min/cm2).
  • The prepared six samples having various pinhole diameters were examined for water permeability using the aforesaid measuring apparatus and also for air permeability using the gurley type densometer.
  • Table 1 shows the measured air permeability, air permeable rate converted from the measured air permeability, the measured water permeability and water permeable rate converted from the measured water permeability.
  • TABLE 1
    air permeability water permeability
    measured air permeable measured water permeable
    Sample value rate value rate
    No. (sec/300 ml) (ml/min./cm2) (ml/min.) (ml/min./cm2)
    1 31.4 81.1 37.05 13
    2 18.3 139.15 67.6 23.72
    3 11.4 223.38 114.34 40.12
    4 9.3 273.81 126 44.21
    5 6.3 404.2 185.35 65.03
    6 5 509.3 233.01 81.75
  • FIG. 4 is a graph showing a relation between the air permeable rate and the water permeable rate. The vertical axis indicates the water permeable rate converted from the measured water permeability, and the horizontal axis indicates the air permeable rate converted from the air permeability measured by the gurley type densometer.
  • As shown in the graph, the water permeable rate can be expressed by a direct function of the air permeable rate. From the direct function, a ratio of the water permeable rate to the air permeable rate is substantially equal to 1/5.5 in a case of the packing material of the present invention.
  • The following examinations were carried out using the air permeable rate capable of converting to the water permeable rate because the measurement of the water permeable rate is a time-consuming process as described above. So, the water permeable rate was expressed as the air permeable rate divided by 5.5.
  • <Relation between the Water Permeability of the Bag and the Temperature of Heat Source>
  • A heat source was produced using each of the prepared bags. And, a relation between the temperature of the heat source and the air permeability of the bags was examined.
  • (1) Heat-Generating Composition
  • As the heat-generating composition, a mixed powder of aluminum powder (#280A, manufactured by MINALCO Co., Ltd.) of 20 g, calcium hydroxide powder (tokusen, manufactured by Tagen lime industry) of 10 g and calcium oxide powder (manufactured by Tagen lime industry) of 20 g and was used.
  • The aluminum powder has the following grain size distribution: -45 μm; 90.80%, 45˜63 μm; 8.30%, 63˜75 μm; 0.64% and +75 μm; 0.25%. The calcium hydroxide powder has the following grain size distribution: ˜45 μm; 4.60%, 45˜75 μm; 21.90%; 75˜150 μm; 35.92% and +150 μm; 37.58%. The calcium oxide powder has the following grain size distribution: ˜75 μm; 15.68%, 75˜150 μm; 34.24% and +150 μm; 50.07%.
  • The calcium oxide powder includes the following elements: calcium oxide (measured by an EDTA titration method (NN indicator)); 93% or more, carbon dioxide (measured by a Storelain method); 2.0% and below and impurities (measured by an EDTA titration method, perchloric acid method, absorption spectroscopy); 3.2% or less. The impurities include silicon dioxide, aluminum oxide, ferric oxide and magnesium oxide.
  • (2) Samples of the Bag
  • The same nonwoven fabric as that used for the measurement of the water permeability was used. By varying a contact depth of the rollers and thus varying the pinhole diameter, the samples of nonwoven fabrics in various air permeable rates, described below, were prepared.
  • Sample 1; 60˜110 (milliliter/min/cm2),
  • Sample 2; 110˜180 (milliliter/min/cm2),
  • Sample 3; 180˜250 (milliliter/min/cm2),
  • Sample 4; 250˜340 (milliliter/min/cm2),
  • Sample 5; 340˜450 (milliliter/min/cm2) and
  • Sample 6; 450˜550 (milliliter/min/cm2).
  • By using the samples, the bag having a receptacle for containing the heat-generating composition was produced. The receptacle had a size of 70 mm×170 mm.
  • (3) Method for Measuring Temperature
  • FIG. 5 is a drawing showing the method for measuring the temperature.
  • The heat source 1, a food F (a retort-packed cooked rice and a 350 millilitter-plastic bottled tea, or a retort-packed cooked rice and a retort-packed curry) and water of 130 g were put in a heating bag 31 having exhaust vents 32. In this example, the heating bag 31 was openable and closable and had two exhaust vents 32 having a diameter of 5 mm. In a temperature-controlled room of which room temperature was kept at 20° C. (in a case of measurement under a low-temperature environment, the temperature was kept at −10˜10° C.), the heating bag 31 was supported in a stainless-steel container 73 set on a heat insulating material 71. And, for 20 minutes after the heat-generating reaction, a temperature T1 in the heating bag 31 (steam temperature), a temperature T2 of the heated water, an environmental temperature T3 and a temperature T4 of the food were measured by the measuring apparatus D.
  • Next, whether the food temperature T4 of each sample satisfied the following heating conditions under the temperature-controlled room was considered.
  • Condition A
  • 1) 40° C. or higher after 5 minutes.
  • 2) 60° C. or higher after 10 minutes.
  • 3) 60° C. or higher after 20 minutes.
  • Condition B
  • 1) 50° C. or higher after 5 minutes.
  • 2) 60° C. or higher after 10 minutes.
  • 3) 65° C. or higher after 20 minutes.
  • Condition C
  • 1) 60° C. or higher after 5 minutes.
  • 2) 65° C. or higher after 10 minutes.
  • 3) 65° C. or higher after 20 minutes.
  • Table 2 shows a result whether the samples satisfied the heating conditions.
  • TABLE 2
    condition A condition B condition C
    40° C. or higher 50° C. or higher 60° C. or higher
    after 5 min. after 5 min. after 5 min.
    60° C. or higher 60° C. or higher 65° C. or higher
    after 10 min. and after 10 min. and after 10 min. and
    Sample 60° C. or higher 65° C. or higher 65° C. or higher
    No. after 20 min. after 20 min. after 15 min.
    1 x x
    2
    3
    4
    5 x x
    6 x x x
  • From these results, the following were obtained:
  • (1) Temperature of the heat source can be controlled by the air permeable rate of the bag.
  • (2) The air permeable rate of the bag required for heating a food is 110 to 340 milliliter/min/cm2 (water permeable rate is about 24 to 44 milliliter/min/cm2).
  • However, even when the air permeable rate is 60 to 450 milliliter/min/cm2 (water permeable rate is about 13 to 65 milliliter/min/cm2), it is possible to heat the food.
  • Moreover, even when the air permeable rate is 60 to 550 milliliter/min/cm2 (water permeable rate is about 13 to 81 milliliter/min/cm2), if the food is small (for example, a retort-packed rice), it is possible to heat such a food.
  • Accordingly, a preferable water permeable rate of the bag for heating a food is 13 to 81 milliliter/min/cm2.
  • It is considered that the heat-generation of the heat-generating composition is caused by a heat-generating reaction of the aluminum after a formation of alkaline environment resulting from hydrolysis of the calcium hydroxide, as described above, and also by a heat-generating reaction of the aluminum activated by a heat-generating resulting from a hydration reaction of the calcium oxide. Under a low-temperature (low-water temperature) condition, either one of the heat-generating reactions alone will not generate sufficient amount of heat. However, when a part of the calcium hydride is replaced by the calcium hydroxide, rate of temperature rise becomes better. The reason is because when the aluminum powder and calcium hydroxide powder exist, while Ca(OH2 has a high water-solubility, since the dissolved Ca(OH)2 hydrolyzes slowly under low-temperature conditions, a dissolution rate of aluminum may be also slow and therefore the reaction of the aluminum powder may be initiated slowly.
  • On the other hand, when the aluminum powder and calcium oxide (CaO) powder exist, Ca(OH)2 produced by a hydration reaction of CaO does not have so high water-solubility because the water temperature rises rapidly to 70 to 80° C. due to heat generated by the aforesaid hydration reaction. Accordingly, although hydrolysis rate is rapid, it requires a longer time until the pH sifts toward alkalis.
  • When the aluminum powder, calcium hydroxide powder and calcium oxide powder exist, Ca(OH)2 dissolves just after the hydrolysis. And, the hydrolysis rate becomes higher due to heat produced by the hydration of CaO and therefore a period until the starting of dissolution of the aluminum becomes shorter. Accordingly, the heat-generating reaction begins rapidly even under low-temperature environments and thus rate of temperature rise can be improved. Therefore, when the water permeable rate of the bag is set smaller than that in a case in which the aluminum powder and calcium oxide powder exist, the temperature lasting ability can be improved.
  • Next, an effect of a construction and amount ratio of the heat-generating composition on the temperature of the heat source under a low-temperature condition (a temperature of water to be reacted is 5° C.) will be described.
  • (1) An Amount Ratio of the Heat-Generating Composition
  • By using the aluminum powder, calcium oxide powder and calcium hydroxide powder used for the aforesaid measurement of water permeability, the following samples were prepared (a total weight of 50 g).
    • (1) Sample 1; aluminum powder:calcium hydroxide powder:calcium oxide powder=50:15:35,
    • (2) Sample 2; aluminum powder:calcium hydroxide powder:calcium oxide powder=60:10:30,
    • (3) Sample 3; aluminum powder:calcium hydroxide powder:calcium oxide powder=60:20:20,
    • (4) Sample 4; aluminum powder:calcium hydroxide powder:calcium oxide powder=40:40:20,
    • (5) Sample 5; aluminum powder:calcium hydroxide powder:calcium oxide powder=40:20:40,
    • (6) Sample 6; aluminum powder:calcium hydroxide powder:calcium oxide powder=50:30:20,
    • (7) Sample 7; aluminum powder:calcium hydroxide powder:calcium oxide powder=60:30:10,
    • (8) Sample 8; aluminum powder:calcium hydroxide powder:calcium oxide powder=30:30:40,
    • (9) Sample 9; aluminum powder:calcium hydroxide powder:calcium oxide powder=30:20:50,
    • (10) Sample 10; aluminum powder:calcium hydroxide powder:calcium oxide powder=35:30:35,
    • (11) Sample 11; aluminum powder:calcium hydroxide powder:calcium oxide powder=35:20:45,
    • (12) Sample 12; aluminum powder:calcium hydroxide powder:calcium oxide powder=40:50:10,
    • (13) Sample 13; aluminum powder:calcium hydroxide powder:calcium oxide powder=45:10:45,
    • (14) Sample 14; aluminum powder:calcium hydroxide powder:calcium oxide powder=45:5:50 and
    • (15) Sample 15; aluminum powder:calcium hydroxide powder:calcium oxide powder=60:5:35.
      (2) Heat-generating ability
  • Each of the sample heat-generating compositions was enclosed with the bag made of base material (a non water-repellent nonwoven fabric (made by 100% rayon, MR-50/PP40,manufactured by Kokko Paper Mfg. Co., Ltd.) having a water permeable rate of about 40 to 44 milliliter/min/cm2) used for measurement of the water permeability. According to the temperature measurement method of FIG. 5, a temperature of the food was measured. In this embodiment, after 25 minutes, in which the reaction continues for 20 minutes and further the heating was kept for 5 minutes, from the heat-generating reaction, a retort-packed rice was measured in temperature in such a manner that a stick type temperature sensor was inserted into the center of the retort-packed rice. Then, whether the samples satisfied the heating condition D (to heat the retort-packed rice to 60° C. or higher after 25 minutes) and condition E (to heat the retort-packed rice to 65° C. after 25 minutes) was discussed.
  • Table 3 shows results whether the samples satisfied the heating conditions.
  • TABLE 3
    condition D condition E
    amount ratio temperature 60° C. or 65° C. or
    Sample calcium calcium (° C.) after 25 higher after higher after
    No. aluminum hydroxide oxide min. 25 min. 25 min.
    1 50 15 35 67.3
    2 60 10 30 72.7
    3 60 20 20 66.5
    4 40 40 20 64.3 x
    5 40 20 40 60.2 x
    6 50 30 20 62.4 x
    7 60 30 10 60.7 x
    8 30 30 40 51.3 x x
    9 30 20 50 51.2 x x
    10 35 30 35 53.5 x x
    11 35 20 45 55.3 x x
    12 40 50 10 56.6 x x
    13 45 10 45 57.7 x x
    14 45 5 50 59.0 x x
    15 60 5 35 58.7 x x
  • Under a low-temperature environment (water temperature is about 5° C.), the following is found.
  • (1) The food heating condition D (to heat the retort-packed rice to 60° C. or higher after 25 minutes) is satisfied when the aluminum powder, calcium hydroxide powder and calcium oxide powder has an amount ratio of 40˜60:10˜40:10˜40.
    (2) The food heating condition E (to heat the retort-packed rice to 65° C. or higher after 25 minutes) is satisfied when the aluminum powder, calcium hydroxide powder and calcium oxide powder has an amount ratio of 50˜60:10˜20:20˜35.
  • Concerning a weight of the heat-generating composition, the following measurement was carried out. The heat-generating composition containing the aluminum powder, calcium hydroxide powder and calcium oxide powder with an amount ratio of the aluminum powder, calcium hydroxide powder and calcium oxide powder being 50:15:35 was enclosed in the bag to prepare the heat sources each having a weight of 30 g, 40 g, 50 g and 60 g. Each of the heat sources was examined in temperature measurement. As a result, all of the heat sources showed substantially the same heat-generating ability. Therefore, a weight of the heat-generating composition is preferably 30 g or larger.
  • EXAMPLE 1
  • FIG. 1 is a drawing showing a structure of a heat source according to the present invention; FIG. 1A is a plane drawing and FIG. 1B is a cross-section drawing.
  • The heat source 1 comprises a bag 10 and a heat-generating composition 20 enclosed in the bag 10.
  • The bag 10 is made of a non water-repellent nonwoven fabric 11 (100% rayon, MR-50/PP40, manufacturedbyKokko Paper Mfg. Co., Ltd.). Almost full area of the bag 10 is punched with pinholes 15 in substantially the uniform density. The pinhole 15 has a diameter of 0.1 to 0.3 mm. The bag 10 has a water permeable rate, measured by the aforesaid method (as shown in FIG. 3), of about 40 milliliter/min/cm2. The water permeable rate can be converted from the air permeable rate measured by the gurley type densometer. The bag 10 has a size of 70 mm×170 mm.
  • The heat-generating composition 30 is a mixed powder of aluminum powder (#280A, manufactured by MINALCO Co., Ltd.) of 25 g, calcium hydroxide powder (tokusen, manufactured by Tagen lime industry) of 7.5 g and calcium oxide powder (manufactured by Tagen lime industry) of 17.5 g (an amount ratio of aluminum:calciumhydroxide:calciumoxide is 50:15:35. A total weight is 50 g). The heat-generating composition 20 is enclosed in the bag 10 to produce the heat source 1.
  • EXAMPLE 2
  • The same heat-generating composition as that of Example (an amount ratio of aluminum:calcium hydroxide:calcium oxide is 50:15:35. A total weight is 50 g) was enclosed in the bag 10 having a water permeable rate of about 81 milliliter/min/cm2 to produce another heat source 3.
  • EXAMPLE 3
  • FIG. 2 is a drawing showing a heating device according to the present invention. In this embodiment, the heating device is used for heating a retort-packed cooked rice and a retort-packed cooked curry.
  • The food heating device 30 comprises a heating bag (container) 31 having exhaust vents 32; the heat source 1 shown in FIG. 1 and water W for activating a heat-generating reaction. In this embodiment, two circular exhaust vents 32 having a diameter of 5 mm are formed. Or, two to four exhaust vents 32 having a diameter of 3 to 7 mm may be formed. Depending on the container, one to two exhaust vents having a diameter of 10 to 15 mm, or eight to ten exhaust vents having a diameter of 1 to 2 mm may be formed. The shape of the exhaust vent is not limited to a circular shape; may be any shape capable of venting water vapor and hydrogen gas. When the bag is a three sided seal pack, the exhaust vent may have a shape formed by turning the opening of the back.
  • The heat source 1 is enclosed in an air-tight outer bag during storing in order to prevent the heat-generating composition from contacting moisture in air.
  • The heat source 1, taken out of the outer bag, the retort-packed cooked rice and the retort-packed cooked curry D were put in the heating bag (container) 31, water of about 5° C. in an amount of 130 g was added and then the container 31 was sealed. The heat source 1 caused a heat-generating reaction to heat the retort-packed cooked rice and retort-packed cooked curry Din the container 31. Water vapor and hydrogen gas produced by the heat-generating reaction were vent through the exhaust vents 32. And, after 25 minutes from the activation of the heat-generating reaction, the retort-packed cocked rice was heated to 67.3° C. And, leakage of the heat-generating composition did not occur.
  • EXAMPLE 4
  • In the same food heating device as that of Example 3, the heat source 3 was used in exchange for the heat source 1. As with Example 3, the heat source 3, taken out of the outer bag, and 350 milliliter-plastic bottled tea D were put in the heating bag (container) 31, water of about 20° C. in an amount of 130 g was added and then the container 31 was sealed. In the same way, the heat source 3, taken out of the outer bag, and a retort-packed cooked rice D were put in the heating bag (container) 31, water of about 5° C. in an amount of 130 g was added and then the container 31 was sealed.
  • FIG. 6 is a graph showing a relation between the measurement time and temperatures.
  • When an initial temperature of the water to be reacted is 20° C., the water temperature rises to 60° C. or higher after 5 minutes from the heat-generating reaction and the risen temperature higher than 80° C. is kept after 10 minutes from the reaction. When an initial temperature of the water to be reacted is 5° C., the water temperature rises to 90° C. after 2 minutes from the heat-generating reaction and the risen temperature higher than 90° C. is kept for about 10 minutes after the reaction. However, the temperature falls down rapidly after 10 minutes and decreases to 50° C. or less after 20 minutes. But, the temperature of the retort-packed rice, which was measured by inserting the stick type temperature sensor into the center of the retort-packed rice after 25 minutes, was 60.4° C. This shows that the retort-packed rice was sufficiently heated.
  • In exchange for the aforesaid non water-repellant nonwoven fabric, another type of non water repellent nonwoven fabric maybe used, for example, CO40s (manufactured by Unitika Co., Ltd.), which has the following properties: basis weight (g/m2); 40, thickness (μm); 330, longitudinal tensile strength (N/5 mm); 35, transverse tensile strength (N/5 mm); 15, longitudinal extensibility (%); 25 and transverse extensibility (%); 75. The nonwoven fabric was made by a spunlaced method.
  • A weight ratio of the aluminum power, calcium hydroxide powder and calcium oxide powder, weight of the heat-generating composition and properties are not limited to the aforesaid values.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a drawing showing a structure of a heat source according to the present invention; FIG. 1A is a plane drawing and FIG. 1B is a cross-section drawing.
  • FIG. 2 is a drawing showing a heating device according to the present invention.
  • FIG. 3 is a drawing showing the water permeable rate measuring method in the present invention.
  • FIG. 4 is a graph showing a relation between the air permeable rate and the water permeable rate.
  • FIG. 5 is a drawing showing the method for measuring the temperature.
  • FIG. 6 is a graph showing a relation between the measurement time and temperatures.
  • EXPLANATION OF ITEM NUMBERS
    • 1,2,3 heat source
    • 10 bag
    • 11 nonwoven fabric
    • 13 water resistant layer
    • 15 pinholes
    • 20 heat-generating composition
    • 30 hood heating device
    • 31 heating bag
    • 32 exhaust vent

Claims (1)

1. A food heating device comprising a heat source and a container having an exhaust vent, in which said heat source is put in said container together with a food to be heated and water is added to said container so that said heat source is reacted with said water to generate heat and to heat the food by the generated heat,
wherein said heat source comprises:
a bag formed by a packing material made of a base material of nonwoven fabric of which one surface is laminated with a waterproof layer, said packing material being punched with a plurality of pinholes, and
a heat-generating composition containing aluminum powder in an amount of 40 to 60% by weight, calcium hydroxide powder in an amount of 10 to 40% by weight and calcium oxide powder in an amount of 10 to 40% by weight, enclosed in said bag,
said packing material has a water permeable rate of 13 to 81 milliliter/min/1 cm2 measured under the following measurement conditions (1) to (4):
(1) ion-exchanged water of 23±3° C. is used,
(2) head of water is 27±0.95 cm,
(3) a water permeable area of said packing material is 2.85 cm2, and
(4) the water permeable amount (milliliter) is defined in such a manner that after an amount of the permeated water per unit time gets constant (after a variation in amount of the permeated water per 10 seconds is within 5% at least consecutive three times), an amount of the permeated water measured in any one minute during the measurement for one minute or more is converted into a water permeable amount (milliliter) using a specific gravity of the ion-exchange water of 1.000 (g/cm3).
US12/085,887 2006-04-21 2007-03-12 Food Heating Device Abandoned US20100147282A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2006-117741 2006-04-21
JP2006117741A JP3921550B1 (en) 2006-04-21 2006-04-21 Food heating equipment
PCT/JP2007/054839 WO2007122900A1 (en) 2006-04-21 2007-03-12 Apparatus for heating food

Publications (1)

Publication Number Publication Date
US20100147282A1 true US20100147282A1 (en) 2010-06-17

Family

ID=38156665

Family Applications (1)

Application Number Title Priority Date Filing Date
US12/085,887 Abandoned US20100147282A1 (en) 2006-04-21 2007-03-12 Food Heating Device

Country Status (6)

Country Link
US (1) US20100147282A1 (en)
EP (1) EP2011846A1 (en)
JP (1) JP3921550B1 (en)
KR (1) KR20080110982A (en)
CN (1) CN101356249A (en)
WO (1) WO2007122900A1 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130226087A1 (en) * 2010-09-15 2013-08-29 David R. King Method and Apparatus for Warming Intravenous Fluids
US20140010483A1 (en) * 2012-07-06 2014-01-09 Kyowa Co., Ltd. Sealing Bag for Hydrogen Gas, and Method for Dissolving Hydrogen Gas
US20140314917A1 (en) * 2011-04-15 2014-10-23 James Richard Allan Pollock Flameless heating composition
US9574764B2 (en) 2012-05-25 2017-02-21 S. C. Johnson & Son, Inc. Portable steam generating device
CN110902158A (en) * 2019-12-11 2020-03-24 安徽省三车节能科技有限公司 Method for improving heating efficiency of calcium oxide heat source in self-heating food

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010222006A (en) * 2007-07-17 2010-10-07 Maikooru Kk Article heater
RU2350244C1 (en) * 2008-01-16 2009-03-27 Общество с ограниченной ответственностью "БАРГАН ПРОДАКШН ГРУПП" (BARGAN PRODUCTION GROUP) Contact heater of packed food products
JP5339888B2 (en) * 2008-12-24 2013-11-13 ダイニック株式会社 Exothermic molded body
KR101102502B1 (en) 2010-04-29 2012-01-05 주식회사 다인 Exothrmic composition
US10863848B2 (en) * 2013-03-15 2020-12-15 Iceburg Point Ventures, LLC Cooking apparatus using liquid bath
WO2015119313A1 (en) * 2014-02-07 2015-08-13 (주)크라우젠 Pouch
CN103844891A (en) * 2014-03-12 2014-06-11 南华大学 Fast egg boiler
WO2015166940A1 (en) * 2014-04-28 2015-11-05 高木 毅 Packaging container
CN106833547B (en) * 2017-02-07 2019-11-01 宁波工程学院 It a kind of food heating self-heating agent and its packs
JP7110690B2 (en) * 2017-04-13 2022-08-02 ライオン株式会社 Non-aqueous exothermic composition and thermal product

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3545457A (en) * 1968-09-26 1970-12-08 Nunziato Schepis Hair curling packages
US3766079A (en) * 1970-10-13 1973-10-16 Smith Inland A O Exothermic composition
US3980070A (en) * 1975-01-08 1976-09-14 Scotty Manufacturing Company Heating pack containing a granular chemical composition
US4080953A (en) * 1976-12-08 1978-03-28 Minnesota Mining And Manufacturing Company Electrochemical heating device
US6200357B1 (en) * 2000-02-17 2001-03-13 Kabushiki Kaisha Kyodo Heating medium and use of the same
US6248257B1 (en) * 1996-08-02 2001-06-19 Tda Research, Inc. Portable heat source
US6309598B1 (en) * 2000-02-08 2001-10-30 Thomas J. Tully Electrochemical heater and method for sterilizing
US6341602B1 (en) * 1999-03-09 2002-01-29 Fred Fulcher Package for flameless heating and heater for the package
US20020104527A1 (en) * 1999-12-14 2002-08-08 Toru Ichikawa Package
US6644383B2 (en) * 2001-06-29 2003-11-11 The Procter & Gamble Company Self-heating/self-cooling package
US20040217325A1 (en) * 2002-05-20 2004-11-04 Kaoru Usui Heating composition and heating element
US20060005827A1 (en) * 2004-05-04 2006-01-12 Candle Corporation Of America Heater product, system and composition
US7258117B2 (en) * 2003-10-17 2007-08-21 Innophos, ,Inc. Heat-producing agglomerates and their application in flameless heaters and self-heating packaging
US20090090350A1 (en) * 2007-10-05 2009-04-09 James A. Donovan Combined food and wipe heater
US20090148570A1 (en) * 2006-02-01 2009-06-11 Tilak Bommaraju Hydrogen elimination and thermal energy generation in water-activated chemical heaters
US7971585B2 (en) * 2006-02-01 2011-07-05 Tilak Bommaraju Hydrogen elimination and thermal energy generation in water-activated chemical heaters

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6443594A (en) * 1987-08-10 1989-02-15 Yoshikazu Munakata Heat-generating composition
JPS6443216A (en) * 1987-08-12 1989-02-15 Yoshikazu Munakata Food heating and warmth keeping structure
JPH01135889A (en) * 1987-11-20 1989-05-29 Mayekawa Mfg Co Ltd Thermal energy storing substance capable of reversible reaction and method for storing and releasing heat
JPH09192026A (en) * 1996-01-24 1997-07-29 Ebaa Corp:Kk Exothermic body
JPH11146835A (en) * 1997-11-18 1999-06-02 Kaihatsu Kogyo Kk Retort food heating agent
JP2000107039A (en) * 1998-09-30 2000-04-18 Hisao Horiguchi Portable heating container
JP2001238906A (en) * 1999-12-24 2001-09-04 Lion Corp Heating element composition, heating element and method for manufacturing the same
JP2002162184A (en) * 2000-11-28 2002-06-07 Asahi Denka Kogyo Kk Heat storage material, heat storing method and heat dissipating method
JP2003342558A (en) * 2002-05-24 2003-12-03 Kyodo:Kk Thermogenic agent
JP2005248383A (en) * 2004-03-04 2005-09-15 Habikkusu Kk Water permeable nonwoven fabric
JP2005290127A (en) * 2004-03-31 2005-10-20 Iwatani Nobuhide Exothermic agent

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3545457A (en) * 1968-09-26 1970-12-08 Nunziato Schepis Hair curling packages
US3766079A (en) * 1970-10-13 1973-10-16 Smith Inland A O Exothermic composition
US3980070A (en) * 1975-01-08 1976-09-14 Scotty Manufacturing Company Heating pack containing a granular chemical composition
US4080953A (en) * 1976-12-08 1978-03-28 Minnesota Mining And Manufacturing Company Electrochemical heating device
US6248257B1 (en) * 1996-08-02 2001-06-19 Tda Research, Inc. Portable heat source
US6341602B1 (en) * 1999-03-09 2002-01-29 Fred Fulcher Package for flameless heating and heater for the package
US20020104527A1 (en) * 1999-12-14 2002-08-08 Toru Ichikawa Package
US6309598B1 (en) * 2000-02-08 2001-10-30 Thomas J. Tully Electrochemical heater and method for sterilizing
US6200357B1 (en) * 2000-02-17 2001-03-13 Kabushiki Kaisha Kyodo Heating medium and use of the same
US6644383B2 (en) * 2001-06-29 2003-11-11 The Procter & Gamble Company Self-heating/self-cooling package
US20040217325A1 (en) * 2002-05-20 2004-11-04 Kaoru Usui Heating composition and heating element
US7258117B2 (en) * 2003-10-17 2007-08-21 Innophos, ,Inc. Heat-producing agglomerates and their application in flameless heaters and self-heating packaging
US20060005827A1 (en) * 2004-05-04 2006-01-12 Candle Corporation Of America Heater product, system and composition
US20090148570A1 (en) * 2006-02-01 2009-06-11 Tilak Bommaraju Hydrogen elimination and thermal energy generation in water-activated chemical heaters
US7971585B2 (en) * 2006-02-01 2011-07-05 Tilak Bommaraju Hydrogen elimination and thermal energy generation in water-activated chemical heaters
US20090090350A1 (en) * 2007-10-05 2009-04-09 James A. Donovan Combined food and wipe heater

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130226087A1 (en) * 2010-09-15 2013-08-29 David R. King Method and Apparatus for Warming Intravenous Fluids
US9642974B2 (en) * 2010-09-15 2017-05-09 The General Hospital Corporation Method and apparatus for warming intravenous fluids
US20140314917A1 (en) * 2011-04-15 2014-10-23 James Richard Allan Pollock Flameless heating composition
US9150772B2 (en) * 2011-04-15 2015-10-06 Julien Philip Goding Flameless heating composition
US9574764B2 (en) 2012-05-25 2017-02-21 S. C. Johnson & Son, Inc. Portable steam generating device
US20140010483A1 (en) * 2012-07-06 2014-01-09 Kyowa Co., Ltd. Sealing Bag for Hydrogen Gas, and Method for Dissolving Hydrogen Gas
US10023360B2 (en) * 2012-07-06 2018-07-17 Hirakimirai Co. Ltd. Sealing bag for hydrogen gas, and method for dissolving hydrogen gas
CN110902158A (en) * 2019-12-11 2020-03-24 安徽省三车节能科技有限公司 Method for improving heating efficiency of calcium oxide heat source in self-heating food

Also Published As

Publication number Publication date
WO2007122900A1 (en) 2007-11-01
KR20080110982A (en) 2008-12-22
JP2007291163A (en) 2007-11-08
JP3921550B1 (en) 2007-05-30
EP2011846A1 (en) 2009-01-07
CN101356249A (en) 2009-01-28

Similar Documents

Publication Publication Date Title
US20100147282A1 (en) Food Heating Device
US20090229594A1 (en) Heat source and heating device
CA2661282C (en) Oxygen activated heater and methods of manufacturing same
US9004059B2 (en) Reusable heater in a package
US4038148A (en) Anaerobic environmental system for bacteria culture testing
US20150241089A1 (en) Transportable device for heating foodstuffs, and a transportable heating element
US4200610A (en) Gas-producing device
CN1681719A (en) Pressure activated reaction vessel and package
EP1648818A1 (en) Reusable apparatus for gas generation
US9050570B2 (en) Device for facilitating a chemical reaction
KR100407582B1 (en) Heating medium and use of the same
JPS60184382A (en) Anaerobic or slightly aerobic environment generation apparatus
JP5314975B2 (en) Chemical exothermic heat generating device and portable food container incorporating chemical exothermic heat generating device
JPWO2007023755A1 (en) Transpiration apparatus and transpiration method
US6309598B1 (en) Electrochemical heater and method for sterilizing
JP2006346329A (en) Heating device and container for portable food incorporating heating device
JP2010183925A (en) Article-heating system
JPH09192026A (en) Exothermic body
CN113150749A (en) Method and device for improving thermal efficiency of aluminum-based heating bag for food
KR100961458B1 (en) Chemical heater and container having the chemical heater
WO2018130623A1 (en) An apparatus for generating hydrogen
JPS6425853A (en) Radiator
JP3100971U (en) Double container
US20220126254A1 (en) Gas micro reactor utilizing membrane packaging
JP3958633B2 (en) Portable food container with heating function

Legal Events

Date Code Title Description
AS Assignment

Owner name: MYCOAL CO., LTD.,JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:URUME, YUKIO;KIMURA, HISAO;TAKAIWA, MIKIO;AND OTHERS;REEL/FRAME:021072/0153

Effective date: 20080331

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION