Packaging method for fruits and vegetables

Abstract

The present invention relates to a method for packaging fruits and vegetables by means of a film endowed with specific permeability and light transmittance properties.

Claims

1. A sealable, thermoplastic film for the packaging of fruits or vegetables comprising: a) a first outer layer comprising between 40 and 60 wt % of a linear low density polyethylene, between 15 and 35 wt % of a medium density polyethylene, and between 15 wt % and 35 wt % of an ethylene-vinyl acetate copolymer, all wt % being based on the weight of the first outer layer; b) a second outer layer comprising between 40 and 60 wt % of a linear low density polyethylene, between 15 and 35 wt % of a medium density polyethylene, and between 15 wt % and 35 wt % of an ethylene-vinyl acetate copolymer, all wt % being based on the weight of the second outer layer; and c) an inner layer comprising between 80 and 97 wt % of a linear low density polyethylene and between 1 and 20 wt % of a low density polyethylene, wherein the total amount of polyethylene in the inner layer is at least 90 wt %, all wt % being based on the weight of the inner layer; the thermoplastic film having: an oxygen transmission rate between 8000 and 14000 cc/sqm.Math.day.Math.atm, measured according to ASTM D-3985 at 23° C. and 0% in-0% out relative humidity, a CO2 transmission rate between 25000 to 41000 cc/sqm.Math.day.Math.atm, measured according to ASTM F-2476, at 23° C. and 0% in-0% out relative humidity, a water vapour transmission rate between 8 and 35 g/sqm.Math.day.Math.atm, measured according to ASTM D1249 at 38° C. and 98% in-0% out relative humidity, and a transmittance of less than 70% of light at wavelengths from the entirety of 200 to 400 nm, measured with the method as follows: 3 cm×1.7 cm pieces of film cut from portions of the film along a transverse direction are put into sample holders of a spectrophotometer equipped with a light source deuterium lamp (190-350 nm) and a halogen lamp (330-900 nm) the spectrophotometer set to have a light wavelength range being 200-850 nm, under the following conditions: resolution of 0.5 nm response: medium scanning speed: 100 nm/min baseline flatness ±0.004 Abs band width: 2 nm photometric mode: absorbance the instrument measured absorbance is converted by an integrated software into % transmittance.

2. The thermoplastic film according to claim 1, wherein the film has a ratio between the CO.sub.2 transmission rate (measured according to ASTM F-2476, at 23° C. and 0% in-0% out relative humidity) and the oxygen transmission rate (measured according to ASTM D-3985 at 23° C. and 0% in-0% out relative humidity) between 2 and 3.8.

3. The thermoplastic film according to claim 1, wherein the film is heat sealable.

4. The thermoplastic film according to claim 1, where the film is cross linked, oriented or heat shrinkable.

5. The thermoplastic film according to claim 1 wherein the film is a multilayer film, comprising a number of layers between 3 and 4.

6. The thermoplastic film according to claim 1, wherein the total thickness of the film is between 5 and 20 microns.

7. The thermoplastic film according to claim 1, wherein the film comprises between 60 and 90 wt % of a polyethylene, selected from linear low density polyethylene (LLDPE), low density polyethylene (LDPE), medium density polyethylene (MDPE) and mixtures thereof.

8. The thermoplastic film according to claim 1, wherein the film is blue coloured, red coloured or green coloured and comprises a blue, red, or green pigment or a blue, red, or green dye inside one or more layers of the film or applied on one or both the surfaces of an outer layers of the film.

9. The thermoplastic film according to claim 1, wherein the film is microperforated, wherein the diameter of the microperforations is comprised between 25 microns and 250 microns.

10. The thermoplastic film according to claim 1 formed into a flexible container by self-sealing the thermoplastic film or by sealing two separate pieces of the thermoplastic film to form a package for packaging fruits and/or vegetables.

11. The thermoplastic film according to claim 10, wherein the flexible container is in the form of a pouch or bag.

12. Method for packaging fruits and/or vegetables comprising the following steps: a) providing a sealable thermoplastic film comprising: i. a first outer layer comprising between 40 and 60 wt % of a linear low density polyethylene, between 15 and 35 wt % of a medium density polyethylene, and between 15 wt % and 35 wt % of an ethylene-vinyl acetate copolymer, all wt % being based on the weight of the first outer layer; ii. a second outer layer comprising between 40 and 60 wt % of a linear low density polyethylene, between 15 and 35 wt % of a medium density polyethylene, and between 15 wt % and 35 wt % of an ethylene-vinyl acetate copolymer, all wt % being based on the weight of the second outer layer; and iii. an inner layer comprising between 80 and 97 wt % of a linear low density polyethylene and between 1 and 20 wt % of a low density polyethylene, wherein the total amount of polyethylene in the inner layer is at least 90 wt %, all wt % being based on the weight of the inner layer; the thermoplastic film having: an oxygen transmission rate between 8000 and 14000 cc/sqm.Math.day.Math.atm, measured according to ASTM D-3985 at 23° C. and 0% in-0% out relative humidity, a CO2 transmission rate between 25000 to 41000 cc/sqm.Math.day.Math.atm, measured according to ASTM F-2476, at 23° C. and 0% in-0% out relative humidity, a water vapour transmission rate between 8 and 35 g/sqm.Math.day.Math.atm, measured according to ASTM D1249 at 38° C. and 98% in-0% out relative humidity, and a transmittance of less than 70% of light at wavelengths from the entirety of 200 to 400 nm, measured with the method as follows: 3 cm×1.7 cm pieces of film cut from portions of the film along a transverse direction are put into sample holders of a spectrophotometer equipped with a light source deuterium lamp (190-350 nm) and a halogen lamp (330-900 nm) the spectrophotometer set to have a light wavelength range being 200-850 nm, under the following conditions: resolution of 0.5 nm response: medium scanning speed: 100 nm/min baseline flatness ±0.004 Abs band width: 2 nm photometric mode: absorbance the instrument measured absorbance is converted by an integrated software into % transmittance, b) running the film through a former thus forming a tube, c) inserting one or more fruits and/or vegetables into the tube, d) sealing the tube longitudinally forming a package, e) sealing and cutting the tube transversally at the beginning and at the end of the package.

13. The method for packaging fruits and/or vegetables according to claim 12, further comprising the following step of flushing an inert gas or a mixture of gases into the packaging between steps c) and e).

14. The method according to claim 12 for packaging fruits selected from the group consisting of bananas and mangoes.

15. A package comprising a sealable thermoplastic film comprising: a) a first outer layer comprising between 40 and 60 wt % of a linear low density polyethylene, between 15 and 35 wt % of a medium density polyethylene, and between 15 wt % and 35 wt % of an ethylene-vinyl acetate copolymer, all wt % being based on the weight of the first outer layer; b) a second outer layer comprising between 40 and 60 wt % of a linear low density polyethylene, between 15 and 35 wt % of a medium density polyethylene, and between 15 wt % and 35 wt % of an ethylene-vinyl acetate copolymer, all wt % being based on the weight of the second outer layer; and c) an inner layer comprising between 80 and 97 wt % of a linear low density polyethylene and between 1 and 20 wt % of a low density polyethylene, wherein the total amount of polyethylene in the inner layer is at least 90 wt %, all wt % being based on the weight of the inner layer; the thermoplastic film having: an oxygen transmission rate between 8000 and 14000 cc/sqm.Math.day.Math.atm, measured according to ASTM D-3985 at 23° C. and 0% in-0% out relative humidity, a CO2 transmission rate between 25000 to 41000 cc/sqm.Math.day.Math.atm, measured according to ASTM F-2476, at 23° C. and 0% in-0% out relative humidity, a water vapour transmission rate between 8 and 35 g/sqm.Math.day.Math.atm, measured according to ASTM D1249 at 38° C. and 98% in-0% out relative humidity, and a transmittance of less than 70% of light at wavelengths from the entirety of 200 to 400 nm, measured with the method as follows: 3 cm×1.7 cm pieces of film cut from portions of the film along a transverse direction are put into sample holders of a spectrophotometer equipped with a light source deuterium lamp (190-350 nm) and a halogen lamp (330-900 nm) the spectrophotometer set to have a light wavelength range being 200-850 nm, under the following conditions: resolution of 0.5 nm response: medium scanning speed: 100 nm/min baseline flatness ±0.004 Abs band width: 2 nm photometric mode: absorbance the instrument measured absorbance is converted by an integrated software into % transmittance, and one or more fruits and/or vegetables packaged in said package.

16. The package according to claim 15, comprising one or more fruits selected from the group consisting of bananas and mangoes.

17. The package according to claim 15, wherein the thermoplastic film is oriented.

18. The package according to claim 15, wherein the thermoplastic film has an oxygen transmission rate between 10000 and 13000 cc/sqm.Math.day.Math.atm, measured according to ASTM D-3985 at 23° C. and 0% in-0% out relative humidity, a CO2 transmission rate between 27000 to 39000 cc/sqm.Math.day.Math.atm, measured according to ASTM F-2476, at 23° C. and 0% in-0% out relative humidity, a water vapour transmission rate between 20 and 30 g/sqm.Math.day.Math.atm, measured according to ASTM D1249 at 38° C. and 98% in-0% out relative humidity, and a transmittance of less than 60% of light at wavelengths from the entirety of 200 to 400 nm, measured with the method as follows: 3 cm×1.7 cm pieces of film cut from portions of the film along a transverse direction are put into sample holders of a spectrophotometer equipped with a light source deuterium lamp (190-350 nm) and a halogen lamp (330-900 nm) the spectrophotometer set to have a light wavelength range being 200-850 nm, under the following conditions: resolution of 0.5 nm response: medium scanning speed: 100 nm/min baseline flatness ±0.004 Abs band width: 2 nm photometric mode: absorbance the instrument measured absorbance is converted by an integrated software into % transmittance.

Description

DESCRIPTION OF DRAWINGS

(1) FIG. 1 represents transmittance at different wavelength values, expressed in nanometers, of Film C-1 and of Films 1-3, described in Example 1, measured as described in Example 2.

(2) FIGS. 2-4 represent bananas before packaging (FIG. 2), 5 days after packaging (DOP5, FIG. 3) and 8 days after packaging (DOP8, FIG. 4), packed in Film 1 (A), Film C-1 (B) or unpacked (C), as described in Example 3.1. FIG. 5 represents the transversal section of bananas 9 days after packaging (DOP9), packed in Film 1 (A), Film C-1 (B) or unpacked (C), as described in Example 3.1. DOP: day of packaging.

(3) FIGS. 6-7 represent bananas 5 days after packaging (DOP5, FIG. 6) and 9 days after packaging (DOP9, FIG. 7), packed in Film 1 (A), Film 2 (B), Film 3 (C) or unpacked (D), as described in Example 3.1. DOP: day of packaging.

(4) FIG. 8 represents the transversal section of bananas 8 days after packaging (DOP8), packed in film C-5 (A) or in film C-6 (B). DOP: day of packaging.

(5) FIG. 9-10 represent mangoes 3 days after packaging (DOP3, FIG. 9) and 11 days after packaging (DOP11, FIG. 10), packed in Film 1 (A), Film C-1 (B) or unpacked (C), as described in Example 3.2. DOP: day of packaging.

DETAILED DESCRIPTION OF INVENTION

(6) A first object of the present invention is the use of a sealable, optionally oriented, thermoplastic film having: an oxygen transmission rate between 8000 and 14000 cc/sqm.Math.day.Math.atm, preferably between 9000 and 13000 cc/sqm.Math.day.Math.atm, more preferably between 10000 and 13000 cc/sqm.Math.day.Math.atm, even more preferably between 11000 and 12000 cc/sqm.Math.day.Math.atm, even more preferably of 11500 cc/sqm.Math.day.Math.atm measured according to ASTM D-3985 at 23° C. and 0% in-0% out relative humidity, a CO.sub.2 transmission rate between 25000 to 41000 cc/sqm.Math.day.Math.atm, preferably between 26000 and 40000 cc/sqm.Math.day.Math.atm, more preferably between 27000 and 39000 cc/sqm.Math.day.Math.atm, even more preferably of 28000 cc/sqm.Math.day.Math.atm, measured according to ASTM F-2476, at 23° C. and 0% in-0% out relative humidity, a water vapour transmission rate between 8 and 35 g/sqm.Math.day.Math.atm, more preferably between 20 and 30 g/sqm.Math.day.Math.atm, even more preferably of 26 g/sqm.Math.day.Math.atm, measured according to ASTM D1249 at 38° C. and 98% in-0% out relative humidity, and a transmittance of less than 70%, preferably less than 60% of light at wavelengths from 100 to 450 nm, preferably from 200 to 450 nm, more preferably from 200 to 400 nm, measured according to the method described in the experimental section,
for the packaging of fruits and/or vegetables.

(7) Preferably, the film according to the invention is used for the packaging of fruits, more preferably for the packaging of fruits selected from the group consisting of bananas and mangoes.

(8) The permeability properties of the film according to the invention may be obtained in various ways, for example by selecting appropriate composition, structure, thickness, orientation and production process of the film or by microperforating the film to form hollow channels spanning the whole thickness of the film (microperforations). The number and the dimension of the microperforations affect the gas permeability of the film. It must also be considered that, to shelter the packed fruits and vegetables from light, the dimensions of the microperforations have to be small enough to prevent light from passing through them and hit directly the products. The microperforations can have any shape, such as circle, square or diamond; typically, they have the shape of circle. Microperforation of the film can be done through any means known in the art and commonly used for this purpose, for example by laser beams or mechanical devices such as rolls equipped with needles. Microperforation is preferably done by laser beams. In an embodiment, the diameter of the microperforations is preferably comprised between 25 microns and 250 microns, more preferably comprised between 70 microns and 200 microns, even more preferably comprised between 50 microns and 150 microns. In the field of packaging films, equipment are known which microperforate a film on the basis of the desired permeability properties; an exemplary equipment is described in WO2011151305.

(9) Preferably, in the film according to the invention the ratio between the CO.sub.2 transmission rate (measured according to ASTM F-2476, at 23° C. and 0% in-0% out relative humidity) and the oxygen transmission rate (measured according to ASTM D-3985 at 23° C. and 0% in-0% out relative humidity) is between 2 and 3.8, more preferably between 2 and 3.6, even more preferably between 2.2 and 3.4.

(10) Preferably, the film according to the invention has an oxygen transmission rate of 11500 cc/sqm.Math.day.Math.atm, a CO.sub.2 transmission rate of 28000 cc/sqm.Math.day.Math.atm and a water vapour transmission rate of 26 g/sqm.Math.day.Math.atm, where the oxygen transmission rate, the CO.sub.2 transmission rate and the water vapour transmission rate are measured as described above.

(11) The film according to the present invention may be a mono or a multilayer film, preferably it is a multilayer film. Preferably, the multilayer film according to the invention comprises a number of layers between 2 and 4, more preferably of 3.

(12) Preferably, the film according to the invention is heat sealable.

(13) Preferably, the film according to the invention is oriented. The oriented film may be mono- or bi-axially oriented, preferably, it is bi-axially oriented.

(14) Preferably, the film of the present invention is cross-linked. Preferably, all the layers of the film are cross-linked.

(15) Preferably, the total thickness of the film is between 5 and 100, 90, 80, 70, 60, 50, 40, 30 or 20 microns, preferably between 5 and 20 microns, more preferably between 10 and 15 microns, more preferably between 12 and 14 microns, even more preferably it is of 13 microns. Preferably, the total thickness of the film is lower than 30, 20, 15 or 10 microns.

(16) The film preferably comprises at least 50 wt % of a polyethylene, with respect to the total composition, preferably selected from linear low density polyethylene (LLDPE), low density polyethylene (LDPE), medium density polyethylene (MDPE) and mixtures thereof. Preferably, the film comprises an ethylene and vinyl acetate copolymer.

(17) When the film has at least two layers, preferably, each of the outer layers of the film comprises at least 50 wt %, preferably between 60 and 90 wt %, more preferably between 70 and 80 wt %, even more preferably 75 wt % of a polyethylene.

(18) Preferably, the polyethylene in the outer layers is selected from linear low density polyethylene (LLDPE) and medium density polyethylene (MDPE) and mixtures thereof. More preferably, said polyethylene is a mixture of LLDPE and MDPE, preferably in a weight ratio of 2:1. Furthermore, said outer layers of the film of the invention preferably further comprise an ethylene and vinyl acetate copolymer in an amount preferably between 15 and 35 wt %, more preferably between 20 and 30 wt %, even more preferably of about 24.5 wt %.

(19) Preferably, the two outer layers of the film have identical composition and thickness.

(20) When the film has more than two layers, preferably at least one of the inner layers of the film of the invention comprises at least 50 wt %, preferably at least 60 wt %, more preferably at least 70 wt %, even more preferably at least 80 wt %, more preferably between 80 and 99 wt %, more preferably between 90 and 98 wt %, even more preferably 97 wt % of a polyethylene. Preferably, the polyethylene in the inner layers is selected from linear low density polyethylene (LLDPE) and low density polyethylene (LDPE) and mixtures thereof. More preferably, said polyethylene is composed for at least 90 wt %, preferably at least 94 wt % of LLDPE.

(21) Example of a suitable low density polyethylene (LLDPE) to be used in the film composition of the invention is for example Dowlex 2045S, commercialised by Dow (Density 0.9200 g/cm.sup.3, Melt flow rate (190° C./2.16 Kg) 1.00 g/10 min; Melting point 124.0° C., Vicat softening point 103° C.).

(22) Example of a suitable medium density polyethylene (MDPE) to be used in the film composition of the invention is for example Dowlex SC 2108G, commercialised by Dow (Density 0.935 g/cm.sup.3, Melt flow rate (190° C./2.16 Kg) 2.6 g/10 min; Melting point 128° C., Vicat softening point 118° C.).

(23) Example of a suitable ethylene and vinyl acetate copolymer is LD362BW by ExxonMobil (Density (23° C.) 0.9275 g/cm.sup.3, Melt flow rate (190° C./2.16 Kg) 2 g/10 min; melting point 104° C.) or EF437AA by Westlake Chemical (Density 0.925 g/cm.sup.3, Melt flow rate (190° C./2.16 Kg) 2 g/10 min).

(24) Preferably, the film of the invention also comprises an antifog additive, for example a glycerol fatty acid ester such as Atmer 129 commercialised by Croda. When the film is multilayer, the antifog agent may be present in the outer and/or inner layers of the film. Preferably, the antifog additive is present in at least one inner layer.

(25) The film of the invention may also comprise one or more antiblock additives, for examples silica, such as Superfine superfloss commercialized by Celite and/or Kemamide E Ultra Bead commercialized by PMC-Biogenix.

(26) The film according to the invention may be heat shrinkable or not. When the film is heat shrinkable, preferably the film has a percentage of free shrink at 120° C. of at least 10%, 20%, 30%, 40% or 50% in longitudinal and/or in transverse direction, measured according to ASTM D2732. Preferably, the film of the invention has a free shrink not higher than 50%, 60%, 70% in longitudinal and/or in transverse direction. A particularly preferred film according to the invention has a free shrink at 120° C. of 60% in longitudinal direction and 65% in transverse direction. For the use in packaging fruits and vegetables according to the present invention, preferably the film is not heat shrinkable.

(27) Preferably, the film according to the first object of the present invention can be manufactured by (co-)extrusion of the single or different layers of the films using either a flat or a circular film die that allows shaping the polymer melt into a thin film or tube, respectively.

(28) Preferably, the film according to the present invention can be manufactured by the so-called double bubble process. According to said process, the multilayer film is co-extruded through a round die, to obtain a tube of molten polymeric material which is quenched immediately after extrusion without being expanded, then heated to a temperature which is above the Tg of all the resins employed and below the melting temperature of at least one of the resins employed, typically by passing it through a hot water bath, or alternatively by passing it through an IR oven or a hot air tunnel, and expanded, still at this temperature by internal air pressure, to get the transversal orientation, and by a differential speed of the pinch rolls which hold the thus obtained “trapped bubble”, to provide the longitudinal orientation. After having been stretched, the film is quickly cooled while substantially retaining its stretched dimensions to somehow freeze the molecules of the film in their oriented state and rolled for further processing. An example of equipment suitable for this technique is disclosed by U.S. Pat. No. 4,841,605.

(29) Alternatively, the multilayer film according to the present invention may be obtained by flat extrusion through a slot die, followed by optional orientation by heating the tape to its softening temperature but below its melt temperature and by stretching in the solid state with a simultaneous or a sequential Tenterframe process. The film is then rapidly cooled to somehow freeze the molecules of the film in their oriented state and wound.

(30) The double bubble process is particularly preferred for the manufacturing of the film of the invention. The seamless tube produced can be directly further processed or converted into a flat film by slitting before being winded into rolls or being further processed.

(31) A particularly preferred film according to the first object of the invention is a film comprising:

(32) a first and second outer layer comprising between 40 and 60 wt %, preferably between 45 and 55 wt %, more preferably 50 wt % of a linear low density polyethylene, between 15 and 35 wt %, preferably between 20 and 30 wt %, more preferably 25 wt % of a medium density polyethylene, between 15 wt % and 35 wt %, preferably between 20 and 30 wt %, more preferably 24.5 wt % of ethylene-vinyl acetate (EVA).
an inner layer comprising between 80 and 97 wt %, preferably between 85 and 95 wt %, more preferably between 90 and 95 wt % of linear low density polyethylene and between 1 and 20 wt %, preferably between 1 and 10 wt %, more preferably between 1 and 5 wt %, even more preferably between 1 and 3% of low density polyethylene, wherein the total amount of polyethylene in the layer is at least 90 wt %, preferably at least 95 wt %.

(33) Preferably, said particularly preferred film consists in the above three layers.

(34) Preferably, in said particularly preferred film, the first and second outer layers have a thickness between 3 and 4 microns and said inner layer has a thickness between 6 and 8 microns.

(35) The film according to the first object of the invention reduces the transmission of light at wavelengths between 100 and 450 nm (UV and blue-violet visible light), in particular at wavelengths between 200 and 450 nm, more in particular at wavelengths between 200 and 400 nm, thus protecting the fruits and vegetables packed in such film against quick ripening and undesired skin color changes.

(36) The light transmittance properties of the film at the above wavelengths may be obtained in various ways, well known to the skilled man. Preferably, the film according to the invention comprises a pigment or a dye inside one or more of its layers or on one or both the surfaces of the outer layers.

(37) For example, suitable pigments or dyes generally known in the art to provide the desired transmittance properties to films and food-approved may be added to the polymer composition of one or more layers of the film before preparing the film or applied on the surface of the preformed film by means of a printing process. Preferably, said pigments or dyes are selected from the group consisting of blue pigments or dyes, red pigments or dyes and green pigments or dyes. In an embodiment, the film of the invention is blue colored. In another embodiment, the film of the invention is red colored. In a further embodiment, the film of the invention is green colored.

(38) In an embodiment, the film of the invention comprises a pigment or a dye inside one or more of its layers. Films where pigments or dyes are incorporated inside one or more layers thereof are generally referred to as “pigmented films”. In order to make the extrusion process of pigmented films easier, pigments or dyes are typically added to a polymer resin or a polymer blend making up such one or more layers, in the form of a masterbatch. Blue pigments or dyes are preferably selected from CI Pigment Blue 60, 64, 66, 16 or 15, CI Direct Blue 86 or CI Solvent Blue 86, 97 or 67.

(39) The pigments or dyes can be added, for example in a polyethylene, low density polyethylene, linear low density polyethylene blend and used to prepare a pigmented film, preferably a blue, red or green film. An example of suitable blend comprising a blue pigment able to provide the desired transmittance properties to the film is product 16103 commercialized by Ampacet, which is a LDPE/LLDPE mixture containing a blue pigment. Another suitable blend comprising a blue pigment is product 161159-U commercialized by Ampacet. Examples of suitable blends comprising a red pigment are product Remafin-Red PE33080765-ZT and product Remafin-Red PE3HDE12020, both commercialized by Clariant. Examples of suitable blends comprising a green pigment are product 174575 commercialized by Ampacet and product Remafin-Green PE63001823-ZN commercialized by Clariant.

(40) In another embodiment, the pigment or dye is included in an ink, which is applied on one or both the surfaces of the preformed film through a printing process. Inks are typically a liquid or a paste and generally comprise, further to the pigments or dyes, solvents, resins, lubricants, solubilizers, surfactants, particulate matter, fluorescents, and other materials. In the context of the present invention, solvent-based inks are generally employed, where the solvents are typically ethyl acetate, isopropanol, ethoxypropanol or mixtures thereof.

(41) Suitable printing process through which the ink can be applied on the surface(s) of the film are, for example, rotogravure or flexography. Films where pigments or dyes—contained in an ink—are applied on one or both the film surfaces are generally referred to as “printed films”.

(42) When the film of the invention is microperforated, and the pigment or dye is applied on the surface(s) of the film through a printing process, microperforation is preferably performed after printing. The printing process may in fact interfere with the microperforation, resulting in the microholes to clog up.

(43) The film of the invention may also comprise a UV-blocker agent. Preferably, the UV-blocker agent is mixed with the pigments or dyes. Accordingly, the UV-blocker agent can be inside one or more of the layers of the film or applied on one or both the surfaces of the outer layers of the film. Example of suitable UV-blockers are products Chimassorb® or Uvinul® commercialized by Basf.

(44) A second object of the invention is the use of a flexible container obtained by self-sealing a film according to the first object of the invention or by sealing two separate pieces of films according to the first object of the invention for packaging fruits and/or vegetables. Preferably, the flexible container according to the second object of the invention is used for packaging fruits, more preferably for packaging fruits selected from the group consisting of bananas and mangoes.

(45) Preferably, the flexible container is in the form of a bag or a pouch.

(46) Any conventional method for making bags and pouches known in the art may be readily adapted to make flexible containers from the film according to the present invention. The self-sealing of the film according to the present invention can be accomplished in a fin seal and/or lap seal mode. When the film is heat sealable, this is obtained preferably by having the heat sealable layer heat sealed to itself, i.e. in a fin seal mode.

(47) The flexible container can be prepared in line, for example using automatic HFFS machine (flowpack) starting from a roll and preparing the single pouch just before being filled with the product to be packaged. Accordingly, a third object of the invention is a method for packaging fruits and/or vegetables comprising the following steps: a) providing the film according to the present invention, b) running the film through a former thus forming a tube, c) inserting one or more fruits and/or vegetables into the tube, d) sealing the tube longitudinally, e) sealing and cutting the tube transversally at the beginning and at the end of the package.

(48) When the film is heat sealable, sealing is preferably performed by heat sealing.

(49) Alternatively, the bags or pouches may be pre-made.

(50) The pre-made bag or pouch can be manufactured, for example, by folding a pre-cut film or by coupling at least two pre-cut films according to the present invention, by subsequently sealing said folded film on two sides or said coupled films on three sides, thus leaving a side of the pre-made bag or pouch open and ready to be filled in with the product to be packaged and, finally, to be closed by a last seal. The pre-made bag or pouch can be sealed according to seal or lap seal mode. When the film is heat sealable, sealing is preferably performed by heat sealing.

(51) Accordingly, a fourth object of the invention is a method for packaging fruits and/or vegetables comprising the following steps: a) introducing one or more fruits and/or vegetables in a flexible container as described above having an open side; b) closing the open side of the container by sealing. When the film is heat sealable, sealing is preferably performed by heat sealing.

(52) Optionally, between steps a) and b), an inert gas or a mixture of gas having a specific composition particularly suitable for the preservation of fruits and/or vegetables can be flushed into the packaging in order to further improve the shelf life of the packaged products.

(53) The fruits and/or vegetables are preferably packed in the flexible container individually. However, also more than one fruits and/or vegetables may be packaged together in the flexible container according to the invention.

(54) Preferably, the methods according to the third and fourth objects of the invention are for packaging fruits, more preferably for packaging fruits selected from the group consisting of bananas and mangoes.

(55) As it will be demonstrated in the experimental section, fruits and vegetables packaged in bags or pouches made with the film of the invention are characterized by a significantly increased shelf life compared to unpackaged products or products packaged in films having different light transmittance and/or permeability properties.

(56) In order to obtain the maximum extension of shelf life, preferably the fruits and/or vegetables are packed in the film or flexible container when still not completely ripe.

(57) A fifth object of the invention is a package comprising a film or flexible container according to the present invention and one or more fruits and/or vegetables packaged in said film or flexible container.

(58) In an embodiment, the package can further comprise a rigid support such as a sheet or a tray. Preferably, such support can be a cardboard sheet or tray.

(59) In an embodiment, the package can further comprise ethylene absorbers and/or ethylene blockers. Both ethylene absorbers and ethylene blockers allow to reduce the ethylene concentrations in the sealed package, thus slowing down maturation/senescence of the packaged products. Ethylene absorbers are chemicals that react with ethylene, which is thus removed and does not accumulate within the package. Ethylene blockers are chemicals which behave as ethylene antagonists, binding to the ethylene receptors of the product and triggering a negative feedback process which stops the production of ethylene by the product itself. Both ethylene absorbers and ethylene blockers are known in the art and commonly used to reduce ethylene content in packaged products. They are generally provided in the form of granules or powder contained in sachets, filters or soaked in films or pads. Typical examples of ethylene absorbers are mixtures of zeolites or clay and oxidizing agents (such as potassium permanganate), like the products commercialized by Retarder. A typical example of ethylene blockers is 1-methylcyclopropene.

EXAMPLES

(60) The present invention can be further understood by reference to the following examples that are merely illustrative and are not to be interpreted as a limitation to the scope of the present invention that is defined by the appended claims.

(61) In the following examples, films made from the ingredients indicated in Table 1 below have been employed:

(62) TABLE-US-00001 TABLE 1 Properties and TRADENAME SUPPLIER Chemical nature ACRONYM parameters SYLOBLOC 47 GRACE Davison AntiBlock Silica- Additive3 Density 2.100 g/cm.sup.3 Amorphous ATMER 129 Croda AntiFog Glycerol Fatty Additive4 Density 0.92 g/cm.sup.3, Acid Ester melting point 69° C. Loxiol LS3 DEO N Emery AntiFog Ethoxylated Additive5 Density (23° C.) Oleochemicals Fatty Alcohol 0.830 g/cm.sup.3 LD362BW ExxonMobil Ethylene Vinyl Acetate EVA2 Density (23° C.) Copolymer with 4.5% 0.9275 g/cm.sup.3, Melt comonomer content flow rate (190° C./2.16 Kg) 2 g/10 min; melting point 104° C. TN2006 Braskem Ethylene Vinyl Acetate EVA3 Density 0.940 g/cm.sup.3, Copolymer with 18% Melt flow rate comonomer content (190° C./2.16 Kg) 0, 7 g/10 min; Melting point 90° C., Vicat softening point 70° C. 1003 VN 4 Total Ethylene Vinyl Acetate EVA4 Density 0.935 g/cm.sup.3, Petrochemicals Copolymer with 13, 5% Melt flow rate comonomer content (190° C./2.16 Kg) 0, 38 g/10 min; melting point 93° C. DOWLEX SC 2108G DOW MDPE MDPE Density 0.935 g/cm.sup.3, Melt flow rate (190° C./2.16 Kg) 2.6 g/10 min; Melting point 128° C., Vicat softening point 118° C. DOWLEX 2045S DOW LLDPE Ethylene-1- LLDPE1 Density 0.920 g/cm.sup.3, octene copolymer Melt flow rate (190° C./2.16 Kg) 1.00 g/10 min; Melting point 124.0° C., Vicat softening point 103° C. AF5841LL TOSAF LLDPE with antifog LLDPE2 Density 0.920 g/cm.sup.3, additive Melt flow rate (190° C./2.16 Kg) 3.0 g/10 min Eltex PF6220AA Ineos LLDPE LLDPE3 Density 0.919 g/cm.sup.3, Melt flow rate (190° C./2.16 Kg) 2.1 g/10 min 16103 Ampacet LDPE/LLDPE mixture Blue in Density 1.5 g/cm.sup.3, with 52% ash and blue LDPE/LLDPE Melt flow rate pigment (190° C./2.16 Kg) 16 g/10 min CESA-PROCESS Clariant LDPE LDPE Density 0.925 g/cm.sup.3, PEA0050633-BN Melt flow rate (190° C./2.16 Kg) 2.1 g/10 min AFFINITY PL 1281G1 DOW VLDPE with slip and VLDPE1 Density 0.9001 g/cm.sup.3, antioxidant additives Melt flow rate 13% comonomer (190° C./2.16 Kg) (octene) 6 g/10 min QUE0 1007 Borealis VLDPE VLDPE2 Density 0.910 g/cm.sup.3, Melt flow rate (190° C./2.16 Kg). 6.6 g/10 min, Melting point 105° C., Viscosity 88 mPa .Math. sec AFFINITY PL 1880G DOW VLDPE VLDPE3 Density 0.902 g/cm.sup.3, Melt flow rate (190° C./2.16 Kg) 1.1 g/10 min, Melting point 99° C., Vicat Softening point 86° C. AFFINITY PL 1850G DOW VLDPE with 12% VLDPE4 Density 0.902 g/cm.sup.3, Comonomer content Melt flow rate (200° C./2.16 Kg) 3 g/10 min, Melting point 97° C., Vicat Softening point 85° C. NUCREL 1202 DuPont Copolymer of ethylene EMAA Density 0.94 g/cm.sup.3, and methacrylic acid, Melt flow rate with 12% comonomer (190° C./2.16 Kg) content 1.5g/10 min, Melting point 99° C., Vicat Softening point 75° C. IXAN PV910 SolVin Polyvinylidene PVDC-MA Density 1.71 g/cm.sup.3, chloride/methyl Viscosity solution acrylate 1.46 mPa .Math. sec ADMER NF927E Mitsui Chemical Maleic Anhydride- LLDPE-md1 Density 0.915 g/cm.sup.3, Modified Linear Melt flow rate LLDPE (190° C./2.16 Kg) 1.3 g/10 min, Vicat Softening point 72° C. BYNEL 4104 (2006) DuPont Maleic Anhydride- LLDPE-md2 Density 0.930 g/cm.sup.3, Modified Melt flow rate Ethylene/Butene (190° C./2.16 Kg) Copolymer 1.10 g/10 min, Melting point 125° C., Vicat Softening point 110° C. SOARNOL AT4403 Nippon Gohsei Ethylene vinyl-alcohol EVOH/EVAL Crystallization point copolymers with 44% 144° C., Density comonomer content 1.140 g/cm.sup.3, Melt (Ethylene) flow rate (at 210° C., 2.16 kg) 3.5 g/10 min, Melting point 164° C. GRILON CF6S EMS-Grivory Copolyamide PA-6\12 Density 1.050 g/cm.sup.3, Melt flow rate (190° C., 5 Kg) 5.75 g/10 min, Melt Volume Index (275° C., 5 Kg) 195 ml/10 min, Melting point 130° C., Relative Viscosity 1.80 GN001 Eastman Polyethylene PETG1 Density 1.27 g/cm.sup.3, Chemical Terephthalate/Glycol Glass Transition 78° C., Viscosity Intrinsic 0.75 dl/g SUKANO G dc S503 Sukano AntiBlock and Slip in PETG2 Density 1.4 g/cm.sup.3, Polyethylene Moisture Content Terephthalate/Glycol max 0, 5%, Vicat softening point 82° C. RAMAPET N180 Indorama Polyethylene PET Density 1.4 g/cm.sup.3, Terephthalate Glass Transition 78° C., Melting Point 245° C., Viscosity Solution 0.80 mPa .Math. sec

Example 1

(63) The following Film 1 according to the invention was prepared having the composition in layers indicated in Table 2 below:

(64) TABLE-US-00002 TABLE 2 Thickness Film Layer (microns) Layer composition Film 1 Layer 1 3.3 10.00% MB2 (98, 20% EVA2, 1, 80% Additive3); 15.00% EVA2; 25.00% MDPE; 50.00% LLDPE1 Layer 2 6.5 94% LLDPE1, 1.00% Additive4, 2.00% Additive5, 3% Blue in LDPE/LLDPE. Layer 3 3.3 10.00% MB2 (98, 20% EVA2, 1, 80% Additive3) 15.00% EVA2; 25.00% MDPE; 50.00% LLDPE1

(65) Film 2 and Film 3 according to the invention were also prepared: their composition in layers is the same as Film 1 above. The free surface of outer layer 3 (i.e the surface which is not adhered to layer 2) was printed with an ink containing a red pigment or a green pigment, respectively, as described in detail below.

(66) As comparative examples, commercial films C-1, C-2, C-3 or C-4, having the composition set out in Table 3, were used.

(67) TABLE-US-00003 TABLE 3 Film C-1 Layer 1 3.3 10.00% MB2 (98, 20% EVA2, 1, 80% Additive3); 15.00% EVA2; 25.00% MDPE; 50.00% LLDPE1 Layer 2 6.5 1.00% Additive4, 2.00% Additive5, 97.00% LLDPE1 Layer 3 3.3 10.00% MB2 (98, 20% EVA2, 1, 80% Additive3) 15.00% EVA2; 25.00% MDPE; 50.00% LLDPE1 Film C-2 Layer 1 9 80.00% VLDPE1; 20.00% VLDPE2 Layer 2 12.8 60.00% VLDPE3; 40.00% EMAA Layer 3 6.8 100.00% EVA3 Layer 4 4.6 100.00% PVDC-MA Layer 5 3.8 100.00% EVA3 Layer 6 8.2 70.00% VLDPE4; 30.00% EVA4 Film C-3 Layer 1 7.1 75.00% LLDPE3, 25.00% LLDPE2 Layer 2 2.2 100.00% LLDPE-md1 Layer 3 2.5 95.00% EVOH/EVAL, 5.00% PA-6\12 Layer 4 2.2 100.00% LLDPE-md1 Layer 5 7.1 75.00% LLDPE3, 25.00% LLDPE2 Film C-4 Layer 1 2.5 58.00% PETG1, 16.00% LLDPE-md2, 24% PET, 2.00% LDPE Layer 2 24 50.00% PET, 50.00% PETG1, Layer 3 6.5 98.00% PET, 2.00% PETG2

(68) Further comparative examples are the colored films C-5 and C-6, commercially available from Creativ Company. They are polyethylene-based films having a colored (blue or red, respectively) polyamide coating. The polyamide coating provides a gas barrier effect, so the gas permeability of Films C-5 and C-6 is lower than the films of the invention, as will be shown below. The thickness of Films C-5 and C-6 is 26 μm.

(69) The layer sequences of Film 1 and of C-1 were extruded on a double bubble line through a round die at 205° C. and at a speed of 28 m/min, cooled at 8° C. and cross linked at 37 KGrays. The obtained tape was then pre-heated by an infrared oven at 100° C., passed through horizontal and vertical ovens heated by steam at 105° C. and air at 134° C., biaxially oriented with stretching ratios of 5.4 in longitudinal direction and 4.9 in transversal direction and stabilized by air rings at 26° C.

(70) Film 2 and Film 3 were manufactured starting from Film 1. In details, samples of Film 1 having dimensions about 210×300 mm were corona treated to increase the surface tension of the film and improve ink adhesion.

(71) The off-line device MINI CORONA TREATER by Boussey Control Europe, set at 22 kV (medium voltage power of the instrument), was used. The treatment time was 0.25 sec from 1 cm of distance from the film.

(72) The corona treated samples were then manually printed on the free surface of outer layer 3 (i.e the surface which is not adhered to layer 2) using the RESOURCE 1 instrument by Resource Color Technology Inc., Jamesburg, N.J., equipped with rod n. 16.

(73) The red ink used was 907445815:RED B420 SANP SAC, supplied by SunChemical. The green ink used was 907446041 GREEN B720 SUNPROP SAC, supplied by SunChemical. The inks as received by the supplier were diluted 1:25 w/w with ethyl acetate.

(74) 10 ml of diluted ink were manually dropped from a Pasteur pipette on each film sample in front of the rod, distributing the ink along the whole width of the sample.

(75) The rod was allowed to roll and spread the ink on the whole area of the film sample. Printed samples were let to dry at room temperature.

(76) Light transmittance of the printed samples was evaluated as described in Example 2 and the results are as shown in FIG. 1.

(77) The layer sequence of Film C-2 was prepared by extrusion coating through a round die. In details, a substrate formed by layers 1 to 3 wherein the heat-sealing layer (layer 1) is the innermost layer of the tube, was co-extruded, quickly quenched with a water cascade, irradiated at a dosage level of 64 kGrays and coated with the sequence of three layers (layer 4 to 6) wherein layer 6 is the outermost layer of the overall tube. The extrusion coated tape was then quenched, re-heated by passing it through a water bath at about 95-98° C., and oriented at this temperature (with orientation ratios of about 3.7:1 in the longitudinal direction and about 4.0:1 in the transverse direction) by the trapped-bubble process.

(78) The layer sequence of Film C-3 was extruded through a round die, quickly quenched at a quenching temperature of 20° C., setting a distance of 10 cm between the die exit and the forming shoe, irradiated at 65 KGrays, biaxially oriented out of hot air at the orientation temperature of 113° C., with stretching ratios of 3.7:1 in both directions, annealed for 3.5 seconds at 70° C., allowing a reduction of the film width in TD of 10%. The film was then cooled at 20° C. The annealing step was carried out on a processing unit as illustrated in FIG. 1 of WO2011029950 consisting of a sequence of six stainless steel Gross Equatherm heated rollers and two cooled rollers, 16-cm in diameter and 203-cm in length, disposed in such a way that the total heating time for the film passing through and contacting the various heated rollers was about 3.5 seconds. The temperature (70° C.) was the same in the three heating zones.

(79) The layer sequence of Film C-4 was manufactured through a Flat Coextrusion process followed by in-line simultaneous Tenterframe orientation. Main operating conditions used to stretch and heat-set the films were: MD ratio: 3.6:1; TD ratio: 3.6:1; Pre-heating temperature: 98° C.; Stretching Temperature: 98° C.; Heat-setting Temperature: 210° C.

(80) The film so obtained was cooled down first by an air flow at 30° C. and then by passing onto a cooling roll that was cooled with water and kept at 20° C.

Example 2

(81) Permeability properties of all the films were measured.

(82) Oxygen Transmission Rate (OTR) measurement was performed according to standard test method ASTM D-3985, under the conditions already described in the description.

(83) CO.sub.2 permeability measurement was performed according to standard test method ASTM F-2476, under the conditions already described above in the description.

(84) Moisture Vapor Transmission Rate (MVTR) measurement was performed according to standard test method ASTM F-1249, under the conditions already described in the description.

(85) The properties of all the films tested are reported in the Table 4 below:

(86) TABLE-US-00004 TABLE 4 CO.sub.2 permeability MVTR at 38° C., OTR 23° C., at 23° C., 98% in-0% out 0% in-0% out RH 0% in-0% out RH relative humidity Film (cc/sqm .Math. day .Math. atm) (cc/sqm .Math. day .Math. atm) (g/sqm .Math. day .Math. atm) Film 1 11500 28000 26 C-1 12000 28000 26 C-2 17 50 7 C-3 25 100 25 C-4 60 50 7 C-5 1500 n.a. 5.1 C-6 1300 n.a. 5.3

(87) Permeability properties (OTR, CO.sub.2 permeability and MVTR) were measured also for Film 2 and Film 3 and resulted to be in line with the values obtained for Film 1.

(88) Also, light transmittance properties of film C-1 and Films 1-3 were measured using a Jasco V-550 spectrophotometer equipped with a light source deuterium lamp (190-350 nm) and a halogen lamp (330-900 nm).

(89) In details, pieces of 3 cm×1.7 cm of the films to be tested were cut from portions of the film spaced one from the other, along the transverse direction of the roll, and put into the sample holder of the instrument. Ten specimens have been tested per each of the films tested.

(90) The light wavelength range tested was 200-850 nm, under the following conditions: resolution of 0.5 nm response: medium scanning speed: 100 nm/min baseline flatness±0.004 Abs band width: 2 nm photometric mode: absorbance. The instrument measures absorbance, which is then converted by an integrated software into % Transmittance.

(91) Ten curves were obtained for each of the films tested, which were substantially superimposed.

(92) FIG. 1 shows one exemplary curve obtained for the films tested.

(93) As can be seen in FIG. 1, Film 1, Film 2 and Film 3 have less than 60% transmittance of light at wavelengths between 200 and 450 nm while Film C-1 has a much higher transmittance in the above wavelength interval. In particular, Film 3 (green colored film) is the one with the lowest transmittance of light in the wavelength interval between about 300 and about 430 nm.

Example 3

(94) The above described films were used to prepare bags (hand made on a manual sealing device, seals were performed leaving an open end for the product manual loading). The above bags were then tested for their effect on shelf life of bananas and mangoes.

Example 3.1

(95) Bananas, belonging to class Extra and having a size of about 21 cm, were purchased when still green.

(96) The different bags described above were used to pack a single banana and the open end was sealed. No gases have been inserted in the package during this operation, that has been performed in air.

(97) The bananas were stored at 20° C. for 9 days after packaging. As a control, unpacked bananas were stored under the same conditions. The external aspect of packed and unpacked bananas was monitored visually 2, 4, 5, 6, 7, 8 and 9 days after packaging. These times courses are indicated in the following as DOP2, DOP4, DOP5, DOP6, DOP7, DOP8 and DOP9, respectively, where DOP means day of packaging. At DOP8 or DOP9, the bananas were dissected and their transversal section was analyzed.

(98) The results of the observations at different time courses are summarized in the Table 5 below. The comments are based on an average of several observed fruits.

(99) TABLE-US-00005 TABLE 5 Peel Peel Peel Peel Peel Peel Transversal Peel Transversal Packaging appearance appearance appearance appearance appearance appearance Section appearance Section film DOP2 DOP4 DOP5 DOP6 DOP7 DOP8 DOP8 DOP9 DOP9 Film 1 Yellow n.a. Yellow Yellow Yellow Yellow n.a. Yellow Commercially acceptable appearance Film 2 n.a. n.a. Yellow Yellow Yellow n.a. n.a. Yellow Commercially acceptable appearance Film 3 n.a. n.a. Yellow Yellow Yellow n.a. n.a. Yellow Commercially acceptable appearance C-1 film Yellow n.a. Yellow Yellow Starting Many n.a. Brown Unacceptable brown brown coloration flecks flecks on about 30% of the surface C-2 film Yellow n.a. Starting n.a. n.a. n.a. n.a. n.a. n.a. brown flecks and unacceptable texture (too soft) C-3 film Yellow n.a. Starting n.a. n.a. n.a. n.a. n.a. n.a. brown flecks and unacceptable texture (too soft) C-4 film Yellow n.a. Yellow n.a. n.a. Starting n.a. Brown Unacceptable brown coloration flecks on more than 50% surface C-5 film n.a. Yellow Yellow but n.a. n.a. Brown Unacceptable n.a. n.a. unacceptable flecks texture (too soft) C-6 film n.a. Yellow Yellow but n.a. n.a. Many Unacceptable n.a. n.a. unacceptable brown texture flecks (too soft) Unpacked Yellow n.a. Yellow with Yellow Brown Brown n.a. Brown Unacceptable brown flecks with brown coloration coloration coloration flecks on more on more on more than 50% than 50% than 50% surface surface surface

(100) The obtained results demonstrate that while the unpacked bananas start to show brown flecks on the peel from DOP5, bananas packed in Film 1 of the invention maintain a yellow peel up to 9 days after packaging. Furthermore, the inner part of bananas packed in Film 1 after 9 days of storage still has a commercially acceptable appearance with a clearer pulp and a thicker skin. Also bananas packed in Film 2 and Film 3 of the invention maintain a yellow peel up to 9 days after packaging and their inner part has a commercially acceptable appearance after 9 days of storage.

(101) Bananas unpacked or packed in packaging films different from the films of the invention have a shorter shelf life. Bananas packed in films with gas barrier properties are commercially unacceptable after 5 days of storage (DOP5), because of a too soft pulp texture. In particular, the pulp of bananas packaged in Films C-5 and C-6 is unacceptably soft, while the external appearance of the fruits is good (yellow peel). In fact C-5 and C-6, being colored, sheltered bananas from light, avoiding flecks formation, but prevented them from exchanging moisture vapor with the environment, which results in a softening of the fruit pulp.

(102) The effect of the Films of the invention on the shelf life of bananas is apparent also from FIG. 2, that shows peel appearance before packaging (FIG. 2), at DOP5 (FIG. 3) and at DOP8 (FIG. 4) and transverse section at DOP9 (FIG. 5) of a banana packed in Film 1 compared to an unpacked banana or a banana packed in film C-1.

(103) FIGS. 6-7 show peel appearance at DOP5 (FIG. 6) and at DOP9 (FIG. 7) of a banana packed in Film 1, a banana packed in Film 2 and a banana packed in Film 3, compared to an unpacked banana.

(104) FIG. 8 shows transverse section at DOP8 of a banana packed in film C-5 and a banana packed in film C-6: the pulp appearance is not compact, with some brown areas.

Example 3.2

(105) Mangoes having a size of about 10-14 cm were purchased when still green.

(106) The bags described above made with Film 1 of the invention and with comparative film C-1 were used to pack a single mango and the open end was sealed. No gases have been inserted in the package during this operation, that has been performed in air.

(107) The mangoes were stored at 20° C. for 11 days. As a control, unpacked mangoes were stored under the same conditions. The external aspect of packed and unpacked mangoes was monitored visually 3 and 11 days after packaging. These times courses are indicated in the following as DOP3 and DOP11, respectively, where DOP means day of packaging.

(108) The results of the observations at different time courses are summarized in the Table 6 below. The comments are based on an average of several observed fruits.

(109) TABLE-US-00006 TABLE 6 Packaging film Peel appearance DOP3 Peel appearance DOP11 Film 1 green green C-1 green green/red Unpacked green yellow/red

(110) The obtained results demonstrate that the mangoes packed in Film 1 of the invention are still unripe after 11 days of storage (DOP11), as demonstrated by their green peel. The unpacked mangoes and the mangoes packed in film C-1 instead are quite ripe at DOP11, showing a peel color typical of a ripening fruit (in particular, unpacked mangoes are riper than mangoes packed in C-1).

(111) Furthermore, the pulp of mangoes packed in Film 1 after 11 days of storage is compact and solid. Mangoes packed in Film C-1 and unpacked mangoes instead have a softer pulp coherently with a more advanced ripening stage. In particular, the pulp of unpacked mangoes is even softer than the pulp of mangoes packed in C-1.

(112) The effect of the films of the invention on the shelf life of mangoes is apparent also from FIGS. 9-10, that show peel appearance at DOP3 (FIG. 9) and at DOP11 (FIG. 10) of a mango packed in Film 1, compared to an unpacked mango or a mango packed in film C-1.