WO2011082059A1 - Procédé de manipulation de bananes - Google Patents

Procédé de manipulation de bananes Download PDF

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Publication number
WO2011082059A1
WO2011082059A1 PCT/US2010/061779 US2010061779W WO2011082059A1 WO 2011082059 A1 WO2011082059 A1 WO 2011082059A1 US 2010061779 W US2010061779 W US 2010061779W WO 2011082059 A1 WO2011082059 A1 WO 2011082059A1
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WO
WIPO (PCT)
Prior art keywords
bananas
map
bags
atmosphere
ethylene
Prior art date
Application number
PCT/US2010/061779
Other languages
English (en)
Inventor
Nazir Mir
Dierdre Holcroft
William James
Alvaro Urena-Padilla
Original Assignee
Rohm And Haas Company
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
Priority to PL10801771T priority Critical patent/PL2519112T3/pl
Priority to KR1020127017727A priority patent/KR101416086B1/ko
Priority to CN2010800531814A priority patent/CN102892298A/zh
Priority to JP2012542247A priority patent/JP5718357B2/ja
Priority to NZ600212A priority patent/NZ600212A/xx
Priority to MX2012005216A priority patent/MX2012005216A/es
Priority to AU2010336964A priority patent/AU2010336964B8/en
Application filed by Rohm And Haas Company filed Critical Rohm And Haas Company
Priority to ES10801771.6T priority patent/ES2683342T3/es
Priority to US13/504,306 priority patent/US9265268B2/en
Priority to RU2012121916/13A priority patent/RU2531604C2/ru
Priority to CA2780728A priority patent/CA2780728C/fr
Priority to SG2012030730A priority patent/SG181419A1/en
Priority to DK10801771.6T priority patent/DK2519112T3/en
Priority to BR112012016149-0A priority patent/BR112012016149B1/pt
Priority to UAA201206469A priority patent/UA105812C2/uk
Priority to EP10801771.6A priority patent/EP2519112B1/fr
Publication of WO2011082059A1 publication Critical patent/WO2011082059A1/fr
Priority to ZA2012/03210A priority patent/ZA201203210B/en
Priority to IL219553A priority patent/IL219553A/en

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Classifications

    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23B—PRESERVING, e.g. BY CANNING, MEAT, FISH, EGGS, FRUIT, VEGETABLES, EDIBLE SEEDS; CHEMICAL RIPENING OF FRUIT OR VEGETABLES; THE PRESERVED, RIPENED, OR CANNED PRODUCTS
    • A23B7/00—Preservation or chemical ripening of fruit or vegetables
    • A23B7/14—Preserving or ripening with chemicals not covered by groups A23B7/08 or A23B7/10
    • A23B7/144—Preserving or ripening with chemicals not covered by groups A23B7/08 or A23B7/10 in the form of gases, e.g. fumigation; Compositions or apparatus therefor
    • A23B7/152—Preserving or ripening with chemicals not covered by groups A23B7/08 or A23B7/10 in the form of gases, e.g. fumigation; Compositions or apparatus therefor in a controlled atmosphere comprising other gases in addition to CO2, N2, O2 or H2O ; Elimination of such other gases
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23B—PRESERVING, e.g. BY CANNING, MEAT, FISH, EGGS, FRUIT, VEGETABLES, EDIBLE SEEDS; CHEMICAL RIPENING OF FRUIT OR VEGETABLES; THE PRESERVED, RIPENED, OR CANNED PRODUCTS
    • A23B7/00—Preservation or chemical ripening of fruit or vegetables
    • A23B7/14—Preserving or ripening with chemicals not covered by groups A23B7/08 or A23B7/10
    • A23B7/153—Preserving or ripening with chemicals not covered by groups A23B7/08 or A23B7/10 in the form of liquids or solids
    • A23B7/154—Organic compounds; Microorganisms; Enzymes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS 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
    • B65D81/00—Containers, 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
    • B65D81/18—Containers, 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 providing specific environment for contents, e.g. temperature above or below ambient
    • B65D81/20—Containers, 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 providing specific environment for contents, e.g. temperature above or below ambient under vacuum or superatmospheric pressure, or in a special atmosphere, e.g. of inert gas
    • B65D81/2069—Containers, 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 providing specific environment for contents, e.g. temperature above or below ambient under vacuum or superatmospheric pressure, or in a special atmosphere, e.g. of inert gas in a special atmosphere
    • B65D81/2084—Containers, 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 providing specific environment for contents, e.g. temperature above or below ambient under vacuum or superatmospheric pressure, or in a special atmosphere, e.g. of inert gas in a special atmosphere in a flexible container
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs

Definitions

  • Bananas are normally harvested by cutting a bunch of bananas from the pseudostem on which it grew. Subsequent to harvest, bunches are often broken down into smaller connected groups called "hands" or, synonymously, “clusters.” It is common to harvest and then ship bananas while the peels are green. Long-distance shipment is often performed at low temperature (for example, at 14°C). Bananas are considered to ripen very slowly during such shipment, during which the bananas normally remain green.
  • Bananas in that condition are ripe but have not developed undesirable post-ripening characteristics such as, for example, one or more of the following: peel with a large number of black spots, black peel, pulp that has turned undesirably brown, or pulp that has turned undesirably soft.
  • step (b) after said step (a), exposing said bananas to an atmosphere that contains one or more cyclopropene compound while said bananas have color stage 2 to 6 on the seven- stage scale,
  • said bananas are kept in a modified-atmosphere package for a time period that includes at least a time interval that lasts for 1 hour, wherein said time interval begins between the conclusion of said step (b) and 72 hours from the conclusion of said step (b), and wherein said modified-atmosphere package is constructed so that the transmission rate of carbon dioxide for the entire package (PCT) is from 2,400 to 120,000 cubic centimeters per day per kilogram of bananas.
  • PCT transmission rate of carbon dioxide for the entire package
  • banana refers to any member of the genus Musa, including, for example, bananas and plantains.
  • ppb (which is equivalent to microliters per liter) denotes parts by volume of that compound per billion parts by volume of the atmosphere.
  • a "polymeric film” is an object made of polymer that is much smaller in one dimension (the “thickness") than in the other two dimensions and that has a relatively uniform thickness.
  • Polymeric film typically has thickness of 1 mm or less.
  • cyclopropene compound is any compound with the formula
  • R 1 , R2 , R 3 and R 4 is independently selected from the group consisting of H and a chemical group of the formula:
  • Each L is a bivalent radical. Suitable L groups include, for example, radicals containing one or more atoms selected from H, B, C, N, O, P, S, Si, or mixtures thereof. The atoms within an L group may be connected to each other by single bonds, double bonds, triple bonds, or mixtures thereof. Each L group may be linear, branched, cyclic, or a combination thereof. In any one R group (i.e., any one of
  • R 1 , R2 , R 3 and R 4 the total number of heteroatoms (i.e., atoms that are neither H nor C) is from 0 to 6.
  • any one R group the total number of non-hydrogen atoms is 50 or less.
  • Each Z is a monovalent radical.
  • Each Z is independently selected from the group consisting of hydrogen, halo, cyano, nitro, nitroso, azido, chlorate, bromate, iodate, isocyanato, isocyanido, isothiocyanato, pentafluorothio, and a chemical group G, wherein G is a 3 to 14 membered ring system.
  • the R 1 , R 2 , R 3 and R 4 groups are independently selected from the suitable groups.
  • the R 1 , R2 , R 3 and R 4 groups may be the same as each other, or any number of them may be different from the others. Groups that are suitable for use as one or more of
  • R 1 , R2", R 3 J and R 4" may be connected directly to the cyclopropene ring or may be connected to the cyclopropene ring through an intervening group such as, for example, a heteroatom-containing group.
  • a chemical group of interest is said to be "substituted” if one or more hydrogen atoms of the chemical group of interest is replaced by a substituent.
  • substituents include, for example, alkyl, alkenyl, acetylamino, alkoxy, alkoxyalkoxy, alkoxycarbonyl, alkoxyimino, carboxy, halo, haloalkoxy, hydroxy, alkylsulfonyl, alkylthio, trialkylsilyl, dialkylamino, and combinations thereof.
  • R 1 , R 2 , R 3 and R 4 groups are, for example, substituted and unsubstituted versions of any one of the following groups: aliphatic, aliphatic-oxy, alkylcarbonyl, alkylphosphonato, alkylphosphato, alkylamino, alkylsulfonyl,
  • alkylcarboxyl alkylaminosulfonyl, cycloalkylsulfonyl, cycloalkylamino, heterocyclyl (i.e., aromatic or non-aromatic cyclic groups with at least one heteroatom in the ring), aryl, hydrogen, fluoro, chloro, bromo, iodo, cyano, nitro, nitroso, azido, chlorato, bromato, iodato, isocyanato, isocyanido, isothiocyanato, pentafluorothio; acetoxy, carboethoxy, cyanato, nitrato, nitrito, perchlorato, allenyl; butylmercapto,
  • R 1 , R 2 , R 3 and R 4 groups are those that contain one or more ionizable substituent groups.
  • ionizable groups may be in non-ionized form or in salt form.
  • R 3 and R 4 are combined into a single group, which is attached to the number 3 carbon atom of the cyclopropene ring by a double bond.
  • one or more cyclopropenes are used in which one or more of R 1 , R2 , R 3 and R 4 is hydrogen.
  • each of R 1 , R2 , R 3 and R 4 is hydrogen or methyl.
  • R 1 is (C1-C4) alkyl and each of R 2 , R 3 , and R 4 is hydrogen.
  • R 1 is methyl and each of R 2 , R 3 , and R 4 is hydrogen, and the cyclopropene compound is known herein as "1-MCP.”
  • a cyclopropene compound is used that has boiling point at one atmosphere pressure of 50°C or lower; or 25°C or lower; or 15°C or lower.
  • a cyclopropene compound is used that has boiling point at one atmosphere pressure of -100°C or higher; -50°C or higher; or 25 °C or higher; or 0°C or higher.
  • an "ethylene- active" compound is a compound that is ethylene or is an ethylene release agent or is a compound with high ethylene activity.
  • MAP modified-atmosphere packaging
  • MAP is an enclosure that alters the gaseous atmosphere inside the enclosure from normal atmospheric composition when respiring produce is contained inside the enclosure.
  • MAP is an enclosure in the sense that it is a package that may be lifted and transported with the produce contained within it.
  • MAP may or may not allow exchange of gas with the ambient atmosphere outside the MAP.
  • MAP may or may not be permeable to diffusion of any particular gas, independent of its permeability or non-permeability to any other gas.
  • a "monomer” is a compound that has one or more carbon- carbon double bond that is capable of participating in a polymerization reaction.
  • an "olefin monomer” is a monomer, the molecules of which contain only atoms of carbon and hydrogen.
  • polar monomer is a monomer, the molecules of which contain one or more polar group. Polar groups include, for example, hydroxyl, thiol, carbonyl, carbon- sulfur double bond, carboxyl, sulfonic acid, ester linkages, other polar groups, and combinations thereof.
  • the method of the present invention involves contacting bananas with one or more ethylene- active compound.
  • Suitable ethylene release agents include, for example, 2-chloroethylphosphonic acid (ethephon), abscisic acid, and other compounds that act in a similar way to affect abscission.
  • Suitable compounds with high ethylene activity include, for example, propylene, vinyl chloride, carbon monoxide, acetylene, 1-butene, and other compounds with high ethylene activity.
  • exposure to ethylene- active compound is performed using ethylene.
  • the preferred temperature for performing exposure of bananas to ethylene- active compound is 13.3°C or higher; more preferably 14°C or higher.
  • the preferred temperature for performing exposure to ethylene-active compound is 18.3°C or lower.
  • Exposure of bananas to ethylene-active compound may be performed by any method.
  • bananas may be in an atmosphere that contains molecules, in gaseous form, of one or more ethylene-active compound.
  • Gaseous ethylene-active compound may be introduced into the atmosphere surrounding the bananas by any method.
  • gaseous ethylene-active compound may be released into the atmosphere in such close proximity to bananas that the ethylene-active compound contacts the bananas before the ethylene-active compound diffuses far away from the bananas.
  • the bananas may be in an enclosure (i.e., and airtight container enclosing a volume of atmosphere), and gaseous ethylene-active compound may be introduced into the enclosure.
  • the bananas are inside a permeable surrounding device, and ethylene-active compound is introduced into the atmosphere outside the permeable surrounding device.
  • the permeable surrounding device encloses one or more bananas and allows some contact between the ethylene-active compound and the bananas, for example by allowing some ethylene-active compound to diffuse through the permeable surrounding device or through holes in the permeable surrounding device or a
  • Such a permeable surrounding device may or may not also qualify as an MAP as defined herein.
  • gaseous ethylene-active compound is introduced into an enclosure
  • the introduction may be performed by any method.
  • the ethylene-active compound may be created in a chemical reaction and vented to the enclosure.
  • ethylene-active compound may be kept in a container such as a compressed-gas tank and released from that container into the enclosure.
  • gaseous ethylene- active compound is introduced into an enclosure that also contains bananas.
  • the preferred concentration of ethylene-active compound in the atmosphere inside the enclosure is 20 ppm or higher; more preferably 50 ppm or higher; more preferably 100 ppm or higher.
  • the preferred concentration of ethylene-active compound in the atmosphere inside the enclosure is 1,000 ppm or less; or 500 ppm or less; or 300 ppm or less.
  • the preferred duration of the exposure of bananas to an atmosphere that contains ethylene-active compound is 8 hours or more; more preferably 16 hours or more; more preferably 20 hours or more.
  • the preferred duration of the exposure of bananas to an atmosphere that contains ethylene-active compound is 48 hours or less; more preferably 36 hours or less; more preferably 24 hours or less.
  • bananas are subjected to a ripening cycle, in which bananas are stored in a normal atmosphere at 18°C or lower for one day or more subsequent to the end of exposure of bananas to an atmosphere that contains ethylene-active compound.
  • a ripening cycle bananas are exposed to an atmosphere containing ethylene- active compound for 20-28 hours at 13.3°C to 18.3°C; bananas are then kept in a normal atmosphere at the same temperature for 20-28 hours; and bananas are then stored in a normal atmosphere at 13.3°C to 20°C for a period of 1 to 6 days.
  • the method of the present invention involves contacting bananas with one or more cyclopropene compound.
  • Such contacting may be performed by any method.
  • bananas may be in an atmosphere that contains molecules, in gaseous form, of one or more cyclopropene compound.
  • Gaseous cyclopropene compound may be introduced into the atmosphere surrounding the bananas by any method.
  • gaseous cyclopropene compound may be released into the atmosphere in such close proximity to bananas that the cyclopropene compound contacts the bananas before the cyclopropene diffuses far away from the bananas.
  • the bananas may be in an enclosure (i.e., and airtight container enclosing a volume of atmosphere), and gaseous cyclopropene compound may be introduced into the enclosure.
  • gaseous cyclopropene compound contacts the bananas
  • the bananas are inside a permeable surrounding device, and cyclopropene compound is introduced into the atmosphere outside the permeable surrounding device.
  • the permeable surrounding device encloses one or more bananas and allows some contact between the cyclopropene compound and the bananas, for example by allowing some cyclopropene compound to diffuse through the permeable surrounding device or through holes in the permeable surrounding device or a combination thereof.
  • a permeable surrounding device may or may not also qualify as an MAP as defined herein.
  • gaseous cyclopropene compound is introduced into an enclosure
  • the introduction may be performed by any method.
  • the cyclopropene compound may be created in a chemical reaction and vented to the enclosure.
  • cyclopropene compound may be kept in a container such as a compressed-gas tank and released from that container into the enclosure.
  • cyclopropene compound may be contained in a powder or pellets or other solid form that contains encapsulated complex of cyclopropene compound in a molecular encapsulation agent. Such a complex is known herein as a "cyclopropene encapsulated complex.”
  • suitable molecular encapsulation agents include, for example, organic and inorganic molecular encapsulating agents.
  • Preferred are organic molecular encapsulation agents.
  • Preferred organic encapsulation agents include, for example, substituted cyclodextrins, unsubstituted cyclodextrins, and crown ethers.
  • encapsulation agents include, for example, zeolites. Mixtures of suitable molecular encapsulation agents are also suitable.
  • the encapsulation agent is alpha cyclodextrin, beta cyclodextrin, gamma cyclodextrin, or a mixture thereof.
  • the preferred encapsulation agent is alpha cyclodextrin.
  • the preferred encapsulation agent will vary depending upon the structure of the cyclodextrin compound or compounds being used. Any cyclodextrin or mixture of cyclodextrins, cyclodextrin polymers, modified cyclodextrins, or mixtures thereof can also be utilized pursuant to the present invention.
  • the amount of molecular encapsulating agent can usefully be characterized by the ratio of moles of molecular encapsulating agent to moles of cyclopropene compound.
  • the ratio of moles of molecular encapsulating agent to moles of cyclopropene compound is 0.3:1 or higher; more preferably 0.9:1 or higher; more preferably 0.92:1 or higher; more preferably 0.95:1 or higher.
  • the ratio of moles of molecular encapsulating agent to moles of cyclopropene compound is 2:1 or lower; more preferably 1.5:1 or lower. In more preferred embodiments, the ratio of moles of molecular encapsulating agent to moles of cyclopropene compound is 0.95:1 to 1.5:1.
  • a cyclopropene compound is introduced into an enclosure that contains bananas by placing cyclopropene encapsulation complex into the enclosure and then contacting the cyclopropene encapsulation complex with a release agent.
  • a release agent is a compound that, when it contacts cyclopropene encapsulation complex, promotes the release of the cyclopropene compound into the atmosphere.
  • water or a liquid that contains 50% or more water by weight, based on the weight of the liquid is an effective release agent.
  • a solid material containing cyclopropene encapsulation complex is placed into an enclosure that contains bananas, and water is brought into contact with that solid material. Contact with the water causes release of cyclopropene into the atmosphere of the enclosure.
  • the solid material may be in the form of tablets that contain, optionally among other ingredients, encapsulation complex that contains a cyclopropene compound and one or more ingredients that causes effervescence.
  • the solid material may be placed into an enclosure that contains bananas, and water vapor in the atmosphere may be effective as a release agent.
  • the solid material that contains cyclopropene encapsulated complex may be in a form that also contains, optionally among other ingredients, a water-absorbing compound such as, for example, a water-absorbing polymer or a deliquescent salt.
  • cyclopropene compound may be dissolved or dispersed in a liquid medium.
  • a cyclopropene may be in an encapsulation complex with a molecular encapsulation agent, and the encapsulation complex may be dissolved or dispersed in a liquid medium.
  • atmosphere containing one or more cyclopropene compound in gaseous form is in contact with bananas (or is in contact with a permeable surrounding device that surrounds one or more banana).
  • all concentrations above zero of cyclopropene compound are
  • the concentration of cyclopropene compound is 0.5 ppb or higher; more preferably is 1 ppb or higher; more preferably is 10 ppb or higher; more preferably 100 ppb or higher.
  • the concentration of cyclopropene compound is 100 ppm or lower, more preferably 50 ppm or lower, more preferably 10 ppm or lower, more preferably 5 ppm or lower.
  • MAP may be active or passive. Active MAP is packaging that is attached to some material or apparatus that adds certain gas or gases to the atmosphere inside the MAP and/or removes certain gas or gases from the atmosphere inside the MAP.
  • Passive MAP takes advantage of the fact that bananas respire after harvest. Thus bananas placed in an enclosure, among other processes, consume oxygen and produce carbon dioxide.
  • the MAP can be designed so that diffusion through the solid exterior surfaces of the MAP and passage of gas through any perforations that may be present in the exterior surface of the MAP maintain optimum levels of oxygen, carbon dioxide, and optionally other gases (such as, for example, water vapor or ethylene or both).
  • passive MAP is used.
  • MAP may be either active or passive.
  • a passive MAP that has that gas transmission characteristic
  • an active MAP that, when it contains bananas, maintains the same atmosphere within itself that would occur in a passive MAP that had that gas
  • a useful way to characterize the MAP is the gas transmission rate of the MAP itself in relation to the amount of bananas held in the MAP.
  • the rate of transmission of carbon dioxide is, in units of cubic centimeters per day per kilogram of bananas, 2,400 or higher; more preferably 5,000 or higher; more preferably 8,000 or higher.
  • the rate of transmission of carbon dioxide is, in units of cubic centimeters per day per kilogram of bananas, 120,000 or lower; more preferably 90,000 or lower.
  • the rate of transmission of oxygen is, in units of cubic centimeters per day per kilogram of bananas, 2,000 or higher; more preferably 4,000 or higher; more preferably 6,000 or higher.
  • the rate of transmission of oxygen is, in units of cubic centimeters per day per kilogram of bananas, 100,000 or lower; or 70,000 or lower.
  • film beta ratio is the ratio of the GT-30 for oxygen gas transmission rate to the GT-30 for carbon dioxide.
  • Preferred polymeric film has film beta ratio of 1:4 or higher.
  • 1:4 or higher is meant that the film beta ratio is 1:X, where X is greater than 4.
  • More preferred MAP is made of material that has film beta ratio of 1:4.5 to 1:8.
  • some or all of the exterior surface of the MAP is polymeric.
  • the polymer is in the form of a polymeric film.
  • Some suitable polymeric films have thickness of 5 micrometer or more; or 10 micrometer or more; or 20 micrometer or more. Independently, some suitable polymeric films have thickness of 200 micrometer or less; or 100 micrometer or less; or 50 micrometer or less.
  • suitable polymer compositions include, for example, polyolefins, polyvinyls, polystyrenes, polydienes, polysiloxanes, polyamides, vinylidene chloride polymers, vinyl chloride polymers, copolymers thereof, blends thereof, and laminations thereof.
  • Suitable polyolefins include, for example, polyethylenes, polypropylenes, copolymers thereof, blends thereof, and laminations thereof.
  • Suitable polyethylenes include, for example, low density polyethylene, ultralow density polyethylene, linear low density polyethylene, metallocene-catalyzed polyethylene, copolymers of ethylene with polar monomers, medium density polyethylene, high density polyethylene, copolymers thereof and blends thereof.
  • Suitable polypropylenes include, for example, polypropylene and oriented polypropylene. In some embodiments, low density polyethylene is used. In some embodiments, copolymer of styrene and butadiene is used.
  • Preferred polymer compositions contain one or more polyolefin; more preferred is polyethylene; more preferred is metallocene-catalyzed polyethylene. More preferred polymer compositions contain one or more polyolefin and one or more copolymer of an olefin monomer with a polar monomer.
  • copolymer herein is meant the product of copolymerizing two or more different monomers. Suitable copolymers of an olefin monomer with a polar monomer include, for example, such polymers available from DuPont called ElvaloyTM resins. Preferred are copolymers of ethylene with one or more polar monomer.
  • Suitable polar monomers include, for example, vinyl acetate, methyl acrylate, ethyl acrylate, butyl acrylate, acrylic acid, methacrylic acid, and mixtures thereof.
  • Preferred polar monomers contain one or more ester linkage; more preferred is vinyl acetate.
  • the preferred amount of polar monomer is, by weight based on the weight of the copolymer, 1% or more; more preferably 2% or more; more preferably 3% or more.
  • the preferred amount of polar monomer is, by weight based on the weight of the copolymer, 18% or less; more preferably 15% or less; more preferably 12% or less; more preferably 9% or less; more preferably 7% or less.
  • polymeric film is used that has no perforations.
  • the polymeric film is chosen or designed so that, when bananas are placed inside a container comprising polymeric film, levels of oxygen and/or carbon dioxide are maintained that preserve the desirable condition of the bananas better than ambient atmosphere would.
  • a container comprises polymeric film
  • the film is arranged so that molecules that are capable of diffusing through the polymeric film will diffuse between the inside of the container and the outside of the container in both directions.
  • a container may be constructed so that one, two, or more separate portions of the surface area of the container consist of polymeric film, and the polymeric film portions may be the same composition as each other or may be different from each other. It is contemplated that such containers will be constructed so that the portion of the container surface that is not polymeric film will effectively block diffusion of gas molecules (i.e., the amount of gas molecules that diffuse through will be of negligible importance).
  • 23°C, in units of cm 3 /(m 2 -day), is 800 or higher; more preferred is 4,000 or higher; more preferred is 5,000 or higher; more preferred is 10,000 or higher; more preferred is 40,000 or higher.
  • MAP beta ratio is defined herein as the ratio of the rate of transmission of oxygen of the MAP itself to the rate of transmission of carbon dioxide of the MAP itself.
  • the MAP beta ratio is 1:1.03 or higher (i.e., 1:Y, where Y is greater than or equal to 1.03); more preferably 1:1.05 or higher.
  • the MAP beta ratio is 1:5 or lower; more preferably 1:3 or lower.
  • polymeric film is used that has perforations.
  • the holes have mean diameter of 5 micrometers to 500 micrometers.
  • the holes have mean diameter of 10 micrometers or more; more preferably 20 micrometers or more; more preferably 50 micrometers or more; more preferably 100 micrometers or more.
  • the holes have mean diameter 300 micrometers or less; more preferably 200 micrometers or less. If a hole is not circular, the diameter of the hole is considered herein to be 2 times the square root of the quotient of the area of the hole divided by pi.
  • the MAP comprises polymeric film that is perforated.
  • the preferred number of holes is determined in part by the weight of bananas that will be present in the MAP.
  • the number of holes per kilogram of bananas in the MAP enclosure is 10 or more; more preferably 20 or more; more preferably 40 or more.
  • the number of holes per kilogram of bananas in the MAP enclosure is 300 or fewer; more preferably 150 or fewer.
  • the preferred total area of the holes, in units of square micrometer per kilogram of bananas is 50,000 or more; more preferably 100,000 or more; more preferably 150,000 or more.
  • the preferred total area of the holes, in units of square micrometer per kilogram of bananas is 6,000,000 or less; more preferably 3,000,000 or less; more preferably 2,000,000 or less.
  • the MAP comprises polymeric film, and the percent of the surface area of the MAP that consists of the polymeric film is 10% to 100%; more preferably 50% to 100%; more preferably 75% to 100%; more preferably 90% to 100%.
  • An MAP in which 90% to 100% of the surface area consists of polymeric film is known herein as a "bag.”
  • MAP that comprise polymeric film and in which all portions of the surface of the MAP that are not polymeric film effectively block diffusion of gas molecules.
  • the MAP is considered to be passive MAP.
  • Holes in polymeric film may be made by any method. Suitable methods include, for example, laser perforation, hot needles, flame, low-energy electrical discharge, and high-energy electrical discharge.
  • One preferred method is laser perforation.
  • laser perforation it is preferred to design or select polymeric film that is well suited to laser perforation. That is, the polymeric film is designed or selected so that the laser easily makes holes that are round and have predictable size.
  • Preferred laser is a carbon dioxide laser.
  • the appropriate wavelenghth of laser light may be chosen.
  • For polymeric films that contain polyethylene and/or copolymers of ethylene with one or more polar monomer it is preferred to choose a carbon dioxide laser producing infrared light that includes infrared light of wavelength 10.6 micrometer.
  • the bananas used in the practice of the present invention may be any members of the genus Musa.
  • edible fruits of the genus Musa are used.
  • plantains or bananas that are not plantains are used.
  • bananas that are not plantains are used.
  • bananas of the species M. acuminata Colla or the hybrid M. X paradisiaca L. are used.
  • members of one or more of the following varieties of banana are used: Sucrier, Lady Finger, Gros Michel, Cavendish (including, for example, Dwarf Cavendish, Giant Cavendish, Pisang masak hijau, Robusta, or Valery), Bluggoe, Ice Cream, Mysore, Salembale, Rasabale, Pachabale, Chandrabale, Silk, Red, Fehi, Golden Beauty, or Orinoco.
  • one or more variety of plantains is used, including, for example, French plantain, Horn plantain, Maaricongo, Common Dwarf, Pelipita, Saba, Harton, Republico-Harton, or Currare.
  • bananas are harvested when they are green.
  • bananas are harvested at 11 to 14 weeks of age.
  • bananas are harvested and immediately placed into MAP.
  • the time from harvest to placement into MAP is 14 days or less, more preferably 7 days or less, more preferably 2 days or less.
  • harvested bananas are placed into MAP prior to shipment, and the harvested bananas remain in the MAP during shipment.
  • bananas are shipped to a destination that is near the intended point of sale to consumers.
  • near the intended point of sale to consumers means a location from which it is capable to transport the bananas to the point of sale to consumers in 3 days or fewer by truck or other surface transportation.
  • bananas are placed into an MAP after harvest and prior to shipment.
  • the MAP may be placed in a carrying device.
  • the carrying device provides some structure for ease of carrying the MAP and for strength in stacking the carrying devices during transportation. Carrying devices allow free exchange of gas between the inside and the outside of the carrying device.
  • a typical suitable carrying device is, for example, a cardboard box with large holes (for example, round holes with diameter 20 mm or greater).
  • bananas are shipped in an MAP that is in a carrying device to a destination near the intended place of sale to consumers.
  • bananas are contacted with a cyclopropene compound while they are in an MAP.
  • bananas are contacted with ethylene- active compound while they are in an MAP and then, while they are in that same MAP, they are subsequently contacted with a cyclopropene compound.
  • bananas are processed as follows. Bananas are exposed to ethylene- active compound and then are allowed to ripen until their color rating is 2 to 6 on the 7-stage scale; those bananas are then exposed to a cyclopropene compound. More preferred is exposing bananas to a cyclopropene compound when the bananas have color rating of 2.5 or higher. More preferred is exposing bananas to a cyclopropene compound when the bananas have color rating of 5.5 or lower; more preferred when the bananas have color rating of 4.5 or lower; more preferred when the bananas have color rating of 3.5 or lower.
  • bananas are exposed to a cyclopropene compound. Subsequent to that exposure to a cyclopropene compound, the bananas are kept in an MAP for a time period that is herein called TPl.
  • TPl includes at least a time interval that is herein called Til.
  • Til is a continuous time interval with duration of 1 hour. That is, the bananas are definitely kept in an MAP for a continuous time interval that lasts 1 hour (Til).
  • the time interval Til is part of a time period TPl that may be the same as Til or that may be larger than Til.
  • TPl is larger than Til, it may be larger by a small amount or a large amount; TPl may be larger than Til by one or more hours, one or more days, or one or more weeks. The time period TPl may begin prior to Til, or TPl may continue after the end of Til, or both.
  • bananas are kept in an MAP for time interval Til, it is meant that, if the bananas are already in an MAP at the beginning of Til, the bananas remain in the MAP throughout Til . It is also meant that, if the bananas are not in an MAP at the beginning of Til, the bananas are placed into an MAP at the beginning of Til and remain therein throughout Til.
  • bananas are kept in an MAP during time interval Til.
  • Til begins after the conclusion of exposing bananas to a cyclopropene compound.
  • Til may begin immediately after the conclusion of exposing bananas to a cyclopropene compound, or Til may begin at any time thereafter, up to 72 hours after the conclusion of exposing the bananas to a cyclopropene compound.
  • the interval between the conclusion of exposing bananas to a cyclopropene compound and the start of Til is 48 hours or less; more preferably 36 hours or less; more preferably 24 hours or less; more preferably 12 hours or less; more preferably 6 hours or less; more preferably 3 hours or less; more preferably 1 hour or less.
  • embodiments described herein with statements that Til starts a certain number hours or less after conclusion of exposing bananas to a cyclopropene compound include embodiments in which bananas are in an MAP during exposure to a cyclopropene compound and remain in the MAP for at least the time interval Til.
  • TP1 extends 11 or more hours beyond the end of Til. That is, bananas remain in an MAP throughout Til and then remain in the MAP for an additional 11 hours or more. In more preferred embodiments, TP1 extends beyond the end of Til by 23 hours or more; more preferably by 47 hours or more; more preferably by 71 hours or more.
  • post-CP bananas are not in MAP during exposure to a cyclopropene compound.
  • pre-CP bananas are in MAP during exposure to a cyclopropene compound. It is contemplated that any post-CP embodiment may be combined with any of the preferred embodiments described herein. It is also contemplated that,
  • any pre-CP embodiment may be combined with any of the preferred embodiments described herein.
  • bananas prior to exposure to a cyclopropene compound, bananas may be placed in any type of container (e.g., any bag, box, enclosure, carrier, or combination thereof), including, for example, containers that are not MAP and/or containers that are MAP.
  • the time from the conclusion of exposure to a cyclopropene compound to the placement of bananas into MAP is 12 hours or less; more preferably 8 hours or less; more preferably 4 hours or less.
  • the time from the conclusion of exposure to a cyclopropene compound to the removal of bananas from MAP is 24 hours or more; more preferably 48 hours or more; more preferably 72 hours or more.
  • bananas are placed into MAP at color stage 4 or lower. For example, if some bananas were to ripen relatively quickly and reach color stage 4 in less than 72 hours after conclusion of exposure to a cyclopropene compound, it would be preferred to place those bananas into MAP as soon as they reached color stage 4 without waiting until 72 hours after conclusion of the exposure to cyclopropene compound.
  • bananas may be placed into MAP at any time prior the beginning of exposure to a cyclopropene compound. Bananas may be placed into an MAP and removed and then re-placed into an MAP prior to the beginning of exposure to a cyclopropene compound. In preferred pre-CP embodiments, bananas are placed into an MAP and then remain in that MAP at least throughout exposure to a cyclopropene and throughout Til. In some pre-CP embodiments, bananas are placed into an MAP prior to exposure to ethylene, and then the bananas remain in that MAP at least throughout exposure to a cyclopropene and throughout Til. In some pre-CP
  • bananas are placed into an MAP at a moment that is either immediately after harvest or is within 2 days after harvest, and then the bananas remain in that MAP at least throughout exposure to a cyclopropene and throughout Til
  • preferred MAP is chosen or designed so that, when bananas are placed into the MAP and the MAP, with the bananas inside, is then exposed ethylene- active compound and exposed to a cyclopropene compound, and then stored for 10 days at 16.7°C, a certain preferred atmosphere will be present in the MAP.
  • the amount of carbon dioxide, by volume based on the volume of the atmosphere inside the MAP is 7% or more; more preferably 8% or more.
  • the amount of carbon dioxide, by volume based on the volume of the atmosphere inside the MAP is 21% or less; more preferably 19% or less.
  • the amount of oxygen, by volume based on the volume of the atmosphere inside the MAP is 6% or more; more preferably 8% or more. In that preferred atmosphere, the amount of oxygen, by volume based on the volume of the atmosphere inside the MAP, is 13% or less; more preferably 12.5% or less.
  • Clusters with rating of 0-1 are commercially desirable to consumers. Clusters with ratings of 2-3 are unacceptable to consumers. In the results below, the average rating for all the clusters in a given treatment group is reported.
  • Bananas may be inspected for the incidence of crown mold. Crown mold is observed and given a numerical rating as follows: 0 (apparently healthy and disease-free fruit); 1 (mycelia not easily detectable with naked eye, but obvious slight disease is visible on the crown); 2 (presence of some visible mycelia on the crown and moderate disease damage on the crown; 3(clearly visible mycelia on the crown with severe disease damage on the crown).
  • Bananas may be inspected for the incidence of crown rot. When disease damage is apparent but no fungus is visible, crown rot is reported, with the degree of damage assessed as follows: 0 (apparently healthy and disease-free fruit); 1 (obvious slight disease is visible on the crown); 2 (moderate disease damage on the crown;
  • stage 1 The color of banana peels is rated according to a seven stage rating scale: stage 1 (dark green); stage 2 (all light green); stage 3 (half green and half yellow); stage 4 (more yellow than green); stage 5 (green tips and necks); stage 6 (all yellow; maybe light green necks, no green tips); stage 7 (yellow flecked with brown). Consumers generally prefer to eat bananas in stage 5 or stage 6.
  • EVA1 ELVAXTM 3124 resin (DuPont Co.), Ethylene/Vinyl Acetate resin with 9% vinyl acetate by weight, based on the weight of the EVA, with melt index (ASTM D1238 190°C / 2.16 kg) of 7 g/10 minute.
  • m-LLDPE EXCEEDTM 1018 resin (Exxon-Mobil Co.), metallocene Linear Low
  • Slip A diatomaceous earth (15% by weight based on the weight of Slip A) in polyethylene.
  • Slip B stearamide (10% by weight based on the weight of Slip B) in
  • Slip-AB Mixture of Slip A and Slip B, with weight ratio of Slip A to Slip B of
  • ELITETM 5400G Enhanced Polyethylene resin (metallocene polyethylene)
  • CN 734 an antiblock containing masterbatch available from several different vendors with targeted amount of 15% diatomaceous earth by weight in 85% polyethylene.
  • CN 706 a stearamide (slip) containing masterbatch available from several different vendors with targeted amount of 10% by weight in 90% ethylene vinyl acetate co-polymer.
  • ELVAX 3170 ethylene-vinyl acetate copolymer available from Dupont
  • 10090 masterbatch available from Ampacet which contains 5% slip in an 8 MI LDPE base resin
  • 10063 masterbatch also available from Ampacet which contains 20% diatomaceous earth in an 8 MI LDPE base resin.
  • MAP bags used in the following Examples were made by producing film, then perforating that film, then making bags from the perforated film.
  • the film was a three-layer coextrudate that was blown to produce film of thickness 29.5 micrometer (1.16 mil). The volume ratio of the layers was this:
  • first layer / second layer / third layer 30/40/30.
  • Each layer was a blend of EVA, m-LLDPE, and, optionally, Slip-AB.
  • the weight ratios were as follows:
  • EVAl/m-LLDPE/Slip-AB 46/52/2
  • the film was perforated using a laser to give average hole diameter of 105 micrometer. Film was folded to form rectangles of 48 cm by 30 cm (18.75 inch by 12 inch) and sealed on three sides to form bags. Each bag had 88 holes.
  • M type MAP bags Two versions of MAP bags were used, herein labeled "M” type MAP bags and “D” type MAP bags. Both types used the similar ingredients and were made as described above; the differences are that they used different grades of metallocene polyethylene and they were made at different facilities. The D bags had holes located differently from the location of holes in the M bags. In the Examples below, if MAP bags are mentioned and the type (i.e., M or D) is not stated, MAP bags of type M were used.
  • the film was drilled with a beam compression laser processing system, and the resulting holes had a machine direction average size of 109 microns and a transverse direction average size of 104 microns. These films were formed into 48 cm by 30 cm (18.75 inch by 12 inch) bags.
  • D-40 A third version of MAP bags was used, herein called "D-40.”
  • the film that was used to make D-40 bags was made as follows. Film was produced on a 7 layer Alpine blown film line. The film is a gusseted tube of 55.9 cm (22 inches wide) with 17.8 cm (7 inch) gussets on each side. Proportions were as follows:
  • the film that was used to make D-40 bags had the following properties:
  • the film was drilled with a beam compression laser processing system, and the resulting holes had a machine direction average size of 124 micrometers and a transverse direction average size of 123 micrometers.
  • D-40 bags were the size that is commonly used to carry 18 kg (40 lb) of bananas. The total number of perforations per bag was 2,735.
  • Example 1 Bananas Placed in MAP at Harvest; Transported Long Distance
  • Bananas were harvested in Columbia and placed in bags. Three types of bags were used:
  • non-MAP polymeric film bag sized to hold 18 kg of bananas ("poly liner").
  • Each bag has two or more holes, each with diameter of approximately 20 mm or larger.
  • the Test Protocol that was used was as follows. 312 MAP bags were packed. Each bag held approximately 1.4 kg (3 lb) of bananas. Thirteen such bags were packed in each box. Total weight of bananas in MAP bags was approximately 432 kg. Approximately 216 kg of bananas were placed into poly liners, which were placed into boxes identical to those used for the MAP bags. Approximately 216 kg of bananas were placed into T bags, which were placed into boxes identical to those used for the MAP bags. The gross fruit weight of the each box was approximately 19.5 kg (43 lb).
  • Banana heads (industry nomenclature is rasimo) were harvested at 14 weeks of age (typical for US markets). Heads were cut into large, medium and small hands. The hands were washed in chlorinated water tanks. The washed hands were further broken into clusters. Clusters were packed into bags that each held approximately 1.4 kg (3 lb) or bags that each held approximately 18 kg (40 lb). Bags were placed into standard cardboard boxes, and each box held approximately 18-20 kg. Each box had 8 round holes of diameter 40 mm, plus two larger oval holes that also served as hand-holds for carrying.
  • the MAP-packaged bananas were packaged as follows: Clusters of approximately 1.4 kg were carefully placed into microperforated bags, and the bags were sealed by twisting the open side of the bag, folding down the twisted end, and placing a rubber band around the twisted and folded end of the bag.
  • Bags were not opened during shipping or ripening. Temperature was monitored in some of the bags by placing a temperature probe in one banana in that bag prior to sealing.
  • Bananas were ripened in forced-air ripening rooms as follows. On day 1, bananas were kept at 18°C (64°F) and exposed to exogenous ethylene (150 ppm for 24 hours). No further exogenous ethylene was used. After day 1, bananas were kept at 18°C for two days and then at 10°C for one day. The temperatures given are pulp temperatures and not room temperatures. Humidity was 85% to 95%.
  • the treatment group with MAP bags and with non-zero MCP are examples of the present invention. All other treatment groups are comparative.
  • each treatment set was marked, placed in a tent in treatment trailer and equilibrated to 10°C (58°F) and 70% to 80% relative humidity. All tents were of equal size and packed the same way. Treatment was for 12 hr.
  • SmartTabsTM tablets were placed in the tent and mixed with water, whereupon the tent was sealed. The amount of SmartTabTM tablets was chosen to achieve the indicated concentration of 1 -methyl cyclopropene in the atmosphere of the tent.
  • the cases were re-palleted and moved into a building at ambient conditions (approximately 20°C) for storage and observation.
  • the cases were opened and bananas re-oriented for evaluation and photography.
  • the cases were placed in the storage room on shelves.
  • Bananas remained in the same bags throughout the packing, treatment in the trailer, and subsequent storage.
  • Example 2 Bananas Packed into MAP at Harvest; Storage to Simulate Shipping
  • Bananas were harvested at 13 weeks of age. Fruit bunches were separated into hands, then washed, and excess latex was removed in chlorinated water tanks using standard commercial practices. The washed hands of bananas were further broken into clusters and treated with fungicide. Clusters were placed into plastic bags; each bag held approximately 1.4 kg (3 lbs) of bananas. The bananas remained in these bags until they were removed for evaluation (see below).
  • the plastic bags were either T bags or were modified-atmosphere bags ("MAP" bags).
  • the T bags also called “PE bags” herein
  • PE bags were typical of bags normally used in commerce for bananas.
  • the bags were then placed into cartons. Each carton held 13 bags. Each carton either held MAP bags only or else held PE bags only. 20 cartons of MAP bags and 20 cartons of PE bags were prepared.
  • the cartons were placed in a refrigerated truck and transported to a storage facility. The distance from harvest to storage was approximately 100 km. The temperature in the refrigerated truck was 14 to 18 °C. To simulate the effect of shipping over long distances, the cartons were placed in conventional cold storage room at 14°C for two weeks. In storage, the cartons were placed so that air could circulate between and around each carton. [0112] After the storage period, the thermostat of the holding room was raised to 18°C, and no further action was taken until the holding room was at 18°C for 12 hours. Bananas were ripened using a 5-day schedule, as follows. The temperatures shown are pulp temperatures; if necessary, the thermostat was lowered so that pulp temperature remained at the desired temperature despite any respiration that may be taking place in the bananas.
  • Treatments with "C” in the treatment number are comparative examples.
  • UTC cartons were placed in a shed that had good ventilation. The remaining cartons remained in the holding room.
  • Four airtight tents were erected in the holding room. Each tent held all the cartons for one of the treatment groups PE-3-C, PE- 10-C, MAP-3, and MAP-10.
  • Example 2A was the same as Example 2A, except that after exposure to 1-MCP, the bananas remained in their bags in the holding room at 14°C for 3 days instead of 4 days.
  • the MAP-3 and MAP-10 groups showed the same type of
  • Example US-1 Bananas Transferred to MAP after Shipment
  • Bananas were harvested and shipped in to Ephrata, Pennsylvania, using standard commercial practices, in standard commercial shipping bags. For shipping, bags were placed in cartons; each carton held sufficient bags so that there were approximately 18.1 kg (40 lb.) of bananas in each carton.
  • Bananas in MAP that received either 300 ppb or 1000 ppb of 1-MCP showed much slower development of color and sugar spots than the bananas in T-bags.
  • Bananas in MAP that received either 300 ppb or 1000 ppb of 1-MCP showed slower development of color and sugar spots after they were removed from their bags than did the bananas in MAP that received zero 1-MCP.
  • the shelf life was extended by 1 to 2 days in bananas with 1-MCP only (i.e., T bags with 1-MCP) or in bananas with MAP only (MAP with zero 1-MCP); the examples of the invention (bananas in MAP that received non-zero 1-MCP) showed extension of shelf life by 8 days.
  • Bananas were harvested and shipped to Ephrata, Pennsylvania as described in Example US-1 above. Upon arrival, bananas were removed from poly liners and placed into one of three types of bags:
  • Bananas in bags were exposed to the ripening cycle described above, except that the first day ("day 0") of the ripening cycle was omitted.
  • the bananas that were exposed to 1- MCP received that exposure when they were at color stage 2 to 2.2.
  • Example US-4 Placement into MAP after exposure to 1-MCP
  • Bananas were harvested and shipped to Ephrata, Pennsylvania as in Example US-1 above. The bananas were also ripened as in Example US-1, except that the bananas remained in the bags in which they were shipped (poly liners) throughout the ripening process. Some of the poly liners were exposed to 1-MCP (1000 ppb) as in Example US-1 above, while others were not. Immediately after the conclusion of the exposure to 1-MCP, bananas were removed from the poly liners, divided into bunches. Some bunches had approximately of 1.4 kg (3 lb) and were placed into T-bags as described above.
  • Example US-5 Various levels of 1-MCP
  • Bananas were grown, shipped, and ripened as described in Example US-1. All bananas were in T-bags through the ripening cycle. At color stage 3.0 to 4.0, the bananas, still in T-bags, were placed in various airtight containers; in each container, a specified concentration of 1-MCP was released into the air; bananas remained in those containers for 12 hours. After that, half of each treatment group was transferred to MAP bags, and all bananas were placed into post-MCP storage as in US-1. At the end of 7 days, bananas were evaluated for sugar spots (SS), color stage (CS), and firmness (F). Firmness was measured with a Fruit Texture Analyzer (Gtiss Company, Republic of South Africa) using a probe of 8 mm diameter. Average results were as follows:
  • the MAP samples showed equal or better color stage (i.e., lower color-stage numbers), better sugar spots (ie., fewer sugar spots), and better firmness (i.e., higher firmness).
  • Example US-7a Various Number of Bananas per Bag (appearance)
  • Bananas were handled and tested as in Example US-1, except that the number of bananas per bag was varied. Concentration of 1-MCP was 1,000 ppb. Also, two different types of MAP bags were used: type M and type D, as described above. Bananas were evaluated on day #7 after treatment with 1-MCP. Average results were as follows:
  • the MAP bags type M and the MAP bags type D perform similarly; no significant difference between them was observed.
  • Bananas were handled and tested as in Example US-1, except that the number of bananas per bag was varied. Also, bananas in MAP bags were compared to "no-bag” bananas (i.e., bananas that were not in any bags after shipping and that went through the ripening, 1-MCP exposure, and storage processes outside of any bag). Also tested were "no MCP” bananas that received no exposure to 1-MCP and that received the same pattern of storage conditions of time and temperature as the bananas exposed to 1- MCP. All bananas were evaluated on day number 5 after the treatment with 1-MCP. Firmness was tested as in Example US-5. Average Results were as follows:
  • Example US-7c Various Number of Bananas per Bag (gas transmission)
  • Bananas were handled and tested as in Example US-1, except that the number of bananas ("# of B") per bag was varied. Results for MAP bags type M were compared at 0 1-MCP ("MAP only") and at 1,000 ppb of 1-MCP ("MAP/MCP"). MAP only samples are comparative; MAP/MCP samples exemplify the present invention. [0142] The gas transmission rates for the entire bag was found by measuring the gas transmission rates for a portion of the perforated film and then making a calculation based on the entire effective area of the bag. Gas transmission rates for the perforated films were measured using quasi-isostatic method as described by Lee et al. (Lee, D. S., Yam, K. L., Piergiovanni, L. "Permeation of gas and vapor," Food Packaging Science and Technology, CRC Press, New York, NY, 2008, pp 100 - 101).
  • POT 0 2 transmission rate of the entire bag (cm 3 /m 2 -day per kg of bananas)
  • PCT C0 2 transmission rate of the entire bag (cm 3 /m 2 -day per kg of bananas)
  • P area total area of perforation of the entire bag (million micrometers squared per kg of bananas)
  • Example US-8 Variations in Hole Locations.
  • Each special bag was made from the same perforated films as used for MAP bags type M. Each special bag had the same dimensions as an MAP type M bag, but each special bag had 196 holes, half of which were blocked using pressure- sensitive adhesive tape. Bags #1 through #12 each had a unique pattern of location of the holes. Bags Dl and D2 were duplicate special bags that re-created the hole pattern of MAP bags type D. Bags Ml and M2 were duplicate special bags that re-created the hole pattern of MAP bags type M. The procedure of Example US-1 was followed, using the special bags as MAP bags.
  • Example US-9 Laser Drilling of perforations.

Abstract

La présente invention concerne un procédé de stockage de bananes comprenant les étapes de (a) exposition desdites bananes à une atmosphère qui contient un ou plusieurs composés d'éthylène actif, et (b) après ladite étape (a), exposition desdites bananes à une atmosphère qui contient un ou plusieurs composés de cyclopropène tandis que lesdites bananes ont un stade de couleur 2 à 6 sur l'échelle à sept stades, où lesdites bananes sont maintenues dans un emballage à atmosphère modifiée pendant une durée qui comprend au moins un intervalle de temps qui dure pendant 1 heure, où ledit intervalle de temps commence entre la conclusion de ladite étape (b) et à 72 heures de la conclusion de ladite étape (b), et où ledit emballage à atmosphère modifiée est construit de sorte que le taux de transmission de dioxyde de carbone pour l'emballage entier (PCT) est de 2 400 à 120 000 centimètres cubes par jour par kilogramme de bananes.
PCT/US2010/061779 2009-12-28 2010-12-22 Procédé de manipulation de bananes WO2011082059A1 (fr)

Priority Applications (18)

Application Number Priority Date Filing Date Title
DK10801771.6T DK2519112T3 (en) 2009-12-28 2010-12-22 PROCEDURE FOR HANDLING BANANAS
CN2010800531814A CN102892298A (zh) 2009-12-28 2010-12-22 处理香蕉的方法
JP2012542247A JP5718357B2 (ja) 2009-12-28 2010-12-22 バナナを取り扱う方法
NZ600212A NZ600212A (en) 2009-12-28 2010-12-22 Method of handling bananas
MX2012005216A MX2012005216A (es) 2009-12-28 2010-12-22 Metodo para manejar platanos.
AU2010336964A AU2010336964B8 (en) 2009-12-28 2010-12-22 Method of handling bananas
RU2012121916/13A RU2531604C2 (ru) 2009-12-28 2010-12-22 Способ обработки бананов
ES10801771.6T ES2683342T3 (es) 2009-12-28 2010-12-22 Método para manipular las bananas
US13/504,306 US9265268B2 (en) 2009-12-28 2010-12-22 Method of handling bananas
PL10801771T PL2519112T3 (pl) 2009-12-28 2010-12-22 Sposób przechowywania bananów
CA2780728A CA2780728C (fr) 2009-12-28 2010-12-22 Procede de manipulation de bananes
SG2012030730A SG181419A1 (en) 2009-12-28 2010-12-22 Method of handling bananas
KR1020127017727A KR101416086B1 (ko) 2009-12-28 2010-12-22 바나나 취급 방법
BR112012016149-0A BR112012016149B1 (pt) 2009-12-28 2010-12-22 Método para o tratamento de bananas
UAA201206469A UA105812C2 (uk) 2009-12-28 2010-12-22 Спосіб обробки бананів
EP10801771.6A EP2519112B1 (fr) 2009-12-28 2010-12-22 Procédé de manipulation de bananes
ZA2012/03210A ZA201203210B (en) 2009-12-28 2012-05-03 Method of handling bananas
IL219553A IL219553A (en) 2009-12-28 2012-05-03 A method of treating bananas

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RU2687795C2 (ru) * 2012-12-18 2019-05-16 Ром Энд Хаас Компани Упаковка с модифицированной атмосферой для бананов
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CN104853610A (zh) * 2012-12-18 2015-08-19 罗姆及哈斯公司 香蕉的气氛调节包装
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WO2016169584A1 (fr) * 2015-04-20 2016-10-27 Waterdiam France Sas Procede de traitement apres-recolte de fruits ou legumes
WO2018166713A1 (fr) * 2017-03-16 2018-09-20 Einenkel / Wirth Gbr Chambre de maturation et procédé pour faire mûrir des fruits
US11576392B2 (en) 2017-03-16 2023-02-14 Einenkel/Wirth Gbr Ripening chamber and method for ripening fruit

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