Maturation or ripening inhibitor release from polymer, fiber, film, sheet or packaging

Abstract

Thermoplastic polyolefin polymer compositions, polymer chips, fibers, woven or nonwoven fabrics, films, closures, and laminates include a polymer and cyclodextrin compound with a volatile maturation inhibitor or an olefinic ethylene receptor antagonist in respiring produce materials. The polymer composition can also include a cyclodextrin-modified polymer or a substituted cyclodextrin. Olefinic ethylene inhibitors can be formed in the cyclodextrin composition, wherein the cyclodextrin releases the olefinic inhibitor composition when used in produce packaging materials. Coating compositions can also be made. The inhibitor is introduced into the materials and is released under controlled conditions of humidity. Upon release, the olefinic inhibitor blocks ethylene receptor sites on proteins that control maturation and can produce an extended period during which the produce does not substantially complete maturation or ripening to a degree leading to spoilage.

Claims

1. A controlled release composition comprising: a cyclodextrin modified thermoplastic polymer comprising a cyclodextrin moiety covalently bonded to a thermoplastic polymer; and 1-methylcyclopropene complexed with the cyclodextrin moiety, wherein the controlled release composition is formed by contacting the cyclodextrin modified thermoplastic polymer comprising less than 800 ppm of water with gaseous 1-methylcyclopropene wherein the contacting is at a molar ratio of about 0.5 moles to about 10 moles of 1-methylcyclopropene per mole of the cyclodextrin moiety, in an enclosed space, at a pressure of about 1 atmosphere to about 15 atmospheres, and at a temperature of about 0 C. to 100 C.

2. The controlled release composition of claim 1 wherein the enclosed space comprises less than about 5 ppm water.

3. The controlled release composition of claim 1 wherein the pressure is about 120 psig.

4. The controlled release composition of claim 1 wherein the contacting is carried out for about 40 hours.

5. The controlled release composition of claim 1 wherein the cyclodextrin modified thermoplastic polymer comprises a cyclodextrin moiety covalently bonded to a polyolefin.

6. The controlled release composition of claim 1 wherein the composition comprises about 0.1 wt % to 20 wt % cyclodextrin.

7. The composition of claim 1 further comprising a thermoplastic polymer, wherein the thermoplastic polymer is contacted with the cyclodextrin modified thermoplastic polymer prior to the contacting with 1-methylcyclopropene.

8. The composition of claim 7 wherein the composition comprises about 1 wt % to 65 wt % of the cyclodextrin modified thermoplastic polymer.

9. The composition of claim 7 wherein the composition comprises about 0.0001 wt % to 3 wt % 1-methylcyclopropene.

10. The composition of claim 7 wherein the cyclodextrin modified thermoplastic polymer comprises a cyclodextrin modified polyolefin and the thermoplastic polymer comprises a polyolefin resin.

Description

DETAILED DESCRIPTION OF THE ILLUSTRATIVE EMBODIMENTS

(1) We have found a thermoplastic composition that can be used as a non-woven fiber or woven fabric, as a film as a packaging material or in a coating there on for the packaging of produce or produce materials for the purpose of extending shelf life or slowing or stopping maturation. The thermoplastic compositions of the invention typically comprise a releasable olefinic antagonist or inhibitor of ethylene generation on produce. The inhibitor is typically introduced into the central pore of a cyclodextrin molecule. The cyclodextrin molecule is typically introduced into the polymer as a small molecule substituted cyclodextrin, a grafted substituent or into the polymer backbone or polymer chain. Such a composition typically comprises about 1.0 to 90 weight percent of a polyolefin and about 0.1 to 65 weight percent or 2 to 50 weight percent of the cyclodextrin grafted resin. The cyclodextrin moiety composition about 0.1 to 20 weight percent or 0.2 to 10 weight percent of the composition as a whole of the polymer composition. In the polymer composition, about 0.005 to 10 weight percent or 0.02 to 5 percent of the available central pores in the cyclodextrin molecule can be occupied by the olefinic inhibitor material. The overall composition of the invention can contain from about 0.01 to about 1 weight percent of the olefinic inhibitor of ethylene generation and produce or produce materials. The olefinic inhibitor itself comprises a compound having from three to about 20 carbon atoms, comprising at least one olefinic bond and comprising a cyclic, olefinic or diazo-diene structure. Typically, the composition can contain about 0.001 to 1 or 0.002 to 0.5 or 0.003 to 0.2 mole of the inhibitor compound preferably 1-MCP per each mole of cyclodextrin in the composition. Specific compounds useful as the olefinic inhibitor of ethylene generation include 1-methyl cyclopropene, 1-butene, 2-butene, isobutylene, etc.

(2) In the manufacture of the polymer compounds of the invention, we have found that careful control of water content in the polymer is important in maintaining the stability of the olefinic inhibitor of ethylene generation in the packaging product. As water is reduced, the olefinic inhibitor is more controllably maintained within the central pore structure of the cyclodextrin material until the material is used as a portion or component of produce or produce component packaging. In the manufacture of the polymer materials, the polymer containing the cyclodextrin moieties can be combined with a thermoplastic polymer material free of the cyclodextrin moieties for the purpose of manufacturing either a master batch of the polymer or the final polymer materials used in manufacturing the fiber fabric film or packaging structures of the invention. In such a composition, the polymer comprising the cyclodextrin moiety can be combined with a thermoplastic polymer. In master batch compositions, the thermoplastic polymer can contain about 1 to 65 weight percent of the thermoplastic containing the cyclodextrin moieties. In a final polymer composition used for forming packaging materials, the polymer composition contains about 0.1 to 20 weight percent of the polymer comprising the cyclodextrin moiety. In such a manufacturing step, the olefinic inhibitor of ethylene generation can be resident in the cyclodextrin molecule (e.g., as a cyclodextrin/olefinic inhibitor masterbatch to be let down into virgin thermoplastics) during the formation of produce containers, packaging or packaging components or after combining cyclodextrin with a thermoplastic material in the conversion process and subsequently loading the cyclodextrin pores with the olefinic inhibitor after the formation of produce containers, packaging or packaging components.

(3) Preferred materials for use in the polymer compositions of the invention are polyolefins and polyolefin copolymers, including polyethylene, polypropylene, poly (ethylene-co-propylene), polyethylene-co-alpha olefin, and other similar homo- and co-polymers of alpha olefins. In one preferred mode, the polymer comprising the cyclodextrin moieties can be manufactured by grafting cyclodextrin onto a maleic anhydride modified polyolefin. Such polyolefins can contain from about 0.5 to about 20 or 0.5 to 10 weight percent maleic anhydride. Such materials can be reacted with cyclodextrin such that a hydroxyl compound of the cyclodextrin material reacts with the maleic anhydride moiety in the polyolefin backbone thus forming a polymer composition such that the maleic anhydride materials are fully reacted to form cyclodextrin modified polyolefins. Such material can contain from about 1 to about 20 weight percent cyclodextrin in the final polymer composition.

(4) An important aspect of the invention is the method for manufacturing or introducing the olefinic inhibitor in the center pore of the cyclodextrin molecule using a process involving controlled low moisture concentration and high pressure at a moderate temperature. In manufacturing the polymer composition of the invention, the polymer comprising of cyclodextrin moiety can be exposed to the olefinic inhibitor at a molar ratio of about 0.5 to 10 moles of inhibitor per mole of cyclodextrin in an enclosed space at a pressure of about 1 to about 15 atmospheres at a temperature of about 0 C. to about 100 C. to effectively introduce the olefinic inhibitor into the central part of the cyclodextrin molecule in amounts discussed above. The moisture can be controlled such that the moisture content of the polymer is <800 ppm and the enclosed space within the treating chamber is less than about 5 ppm moisture. Alternatively the moisture content of the close space is less than about 1 percent relative humidity. In order to release the inhibitor or antagonist, the moisture contact is increased.

(5) Lastly an important aspect of the invention is the method of controlled release of the olefinic inhibitor from packaging components or materials such that an effective concentration of the inhibitor molecule in the enclosed space within the packaging system effectively controls, inhibits or reduces maturation or ripening of the materials. In such a method, the polymer composition with the cyclodextrin compound and the olefinic inhibitor is used in manufacturing a packaging material, the produce or produce material is placed within the packaging material and in the enclosed volume within the packaging material a controlled amount of moisture or humidity is put into place within the packaging as previously descried. The moisture content at typical storage temperatures in this environment causes the release of the olefinic inhibitor from the cyclodextrin molecule. This effective concentration of the olefinic inhibitor in the void space within the packaging material maintains the produce effectively.

(6) The cyclodextrin modified polyolefin compositions or resins can contain a blend of a polymer and a polymer containing cyclodextrin or a substituted cyclodextrin. The Polymer can comprise from about 0.1 to about 20 wt % or preferably 0.3 to 10 wt % cyclodextrin. The thermoplastic polymer compositions comprise a blend of a major proportion of a polyolefin resin and between about 1 wt % to about 65 wt % of a cyclodextrin modified polyolefin resin based on the polymer composition; and from about 0.0001 wt % to about 3 wt %, or about 0.0002 to 2 wt %, or about 0.0005 wt % to about 1 wt % of a volatile olefinic inhibitor or antagonist compound.

(7) Inhibitor Compound

(8) The inhibitor compound of the invention includes a C.sub.4-20 olefin compound, preferably with the double bond adjacent to a terminal carbon atom. Cyclopropene derivatives can act as an inhibitor, such as the following formula I. In formula I, R.sup.1 is independently hydrogen or a C.sub.1-16 alkyl, R.sup.2 is independently hydrogen or a C.sub.1-16 alkyl and R.sup.3 and R.sup.4 are independently hydrogen or a C.sub.1-16 alkyl with a proviso that at least one of R.sup.1 or R.sup.2 is methyl.

(9) ##STR00001##
Cyclodextrin

(10) Cyclodextrin (CD) is a cyclic oligomer of -D-glucopyranoside units formed by the action of certain enzymes such as cyclodextrin glycotransferase (CGTase). Three cyclodextrins (alpha, beta, and gamma) are commercially available consisting of six, seven and eight -1,4-linked glucose monomers, respectively. The most stable three-dimensional molecular configuration for these oligosaccharides is a toroid with the smaller and larger opening of the toroid presenting primary and secondary hydroxyl groups. The specific coupling of the glucose monomers gives the CD a rigid, truncated conical molecular structure with a hollow interior of a specific volume. This internal cavity, which is lipophilic (i.e., is attractive to hydrocarbon materials when compared to the exterior), is a key structural feature of the cyclodextrin, providing the ability to complex molecules (e.g., aromatics, alcohols, halides and hydrogen halides, carboxylic acids and their esters, etc.). The complexed molecule must satisfy the size criterion of fitting at least partially into the cyclodextrin internal cavity, resulting in an inclusion complex.

(11) TABLE-US-00001 CYCLODEXTRIN TYPICAL PROPERTIES CD PROPERTIES -CD -CD -CD Degree of polymerization (n=) 6 7 8 Molecular Size (A) inside diameter 5.7 7.8 9.5 outside diameter 13.7 15.3 16.9 height 7.0 7.0 7.0 Specific Rotation [].sup.25.sub.D +150.5 +162.5 +177.4 Color of iodine complex Blue Yellow Yellowish Brown Solubility in Distilled water 14.50 1.85 23.20 (g/100 mL) 25 C.

(12) The oligosaccharide ring forms a torus, as a truncated cone, with primary hydroxyl groups of each glucose residue lying on a narrow end of the torus. The secondary glucopyranose hydroxyl groups are located on the wide end. The parent cyclodextrin molecule, and useful derivatives, can be represented by the following formula (the ring carbons show conventional numbering) in which the vacant bonds represent the balance of the cyclic molecule:

(13) ##STR00002##

(14) The CD's internal cavity size (i.e., , , ) can be considered and the functional group modification can be suitable for changing the desired bulk polymer and surface polymer characteristics in addition to forming an inclusion complex with targeted volatiles or impurities. To achieve a specific result, more than one cavity size and functional group may be necessary.

(15) According to the present disclosure, the cyclodextrin material is a compound containing as an inclusion complex of the inhibitor or antagonist compound, formed within the central pore of each cyclodextrin moiety in the polymer composition of the invention. The olefinic antagonist or inhibitor compound can comprise a C.sub.4-20 compound having at least one olefinic group. As a result of the inclusion of the olefinic inhibitor compound in the central pore of the cyclodextrin molecule, any polymer composition containing a cyclodextrin moiety can contain a large fraction of the cyclodextrin moiety with the olefinic inhibitor as an inclusion complex within the central pore of the cyclodextrin ring. In certain inventions, the central pore is used as a binding location for permeant but in this invention, the central pore is used as a storage location for the olefinic inhibitor or antagonist which can be controllably released from the polymer composition to control maturation in produce or produce materials.

(16) Cyclodextrin Derivatives

(17) The thermoplastic composition of the invention can contain a cyclodextrin derivative. The cyclodextrin derivative is compatible with the polymer material. The cyclodextrin derivative can be combined with the olefinic inhibitor such that the olefinic inhibitor is formed as an inclusion complex within the central pore. Such polymer materials containing the substituted cyclodextrin can be used in a method of controlled release of the olefinic inhibitor from the composition in control or reduction of ripening of the produce or produce materials. The methods of manufacturing the polymer with a cyclodextrin having the olefinic inhibitor are substantially similar to the polymer compositions containing the cyclodextrin moiety. Further, the polymer compositions containing the substituted cyclodextrin material with the olefinic inhibitor can be used in methods of controlled release of the olefinic inhibitor using substantially similar process steps.

(18) CD molecules have available for reaction with a functionalized polyolefin the primary hydroxyl at the six position of the glucose moiety, and at the secondary hydroxyl in the two and three positions. Because of the geometry of the CD molecule, and the chemistry of the ring substituents, all hydroxyl groups are not equal in reactivity. However, with care and effective reaction conditions, dry CD molecules can be reacted to obtain substituted CD. CD with selected substituents (i.e. substituted only on the primary hydroxyl or selectively substituted only at one or both the secondary hydroxyl groups) can also be grafted if desired. Directed synthesis of a derivatized molecule with two different substituents or three different substituents is also possible. These substituents can be placed at random or directed to a specific hydroxyl. Further, CD alcohol derivatives (e.g., hydroxyethyl and hydroxypropyl) and amino derivatives can be reacted to make a grafted CD.

(19) The preferred preparatory scheme for producing a substituted CD material having compatibility with polyvinyl resin involves reactions at the primary or secondary hydroxyls of the CD molecule. It is meant that a hydroxyl functionality of the CD reacts with the reactive component of the substituent forming compound to form a substituted cyclodextrin reaction product. The formation of a bond on either the primary or secondary ring hydroxyls of the CD molecule involves well-known reactions. The primary OH groups of the cyclodextrin molecules are more readily reacted than the secondary groups. However, the molecule can be substituted on virtually any position to form useful compositions. Broadly, we have found that a wide range of pendant substituent moieties can be used on the molecule. These derivatized cyclodextrin molecules can include alkylated cyclodextrin, hydrocarbyl-amino cyclodextrin, and others. The substituent moiety should include a region that provides compatibility to the derivatized material.

(20) Amino and azido derivatives of cyclodextrin having pendent thermoplastic polymer containing moieties can be used in the sheet, film or container of the invention. The sulfonyl derivatized cyclodextrin molecule can be used to generate the amino derivative from the sulfonyl group substituted cyclodextrin molecule via nucleophilic displacement of the sulfonate group by an azide (N.sub.3.sup.1) ion. The azido derivatives are subsequently converted into substituted amino compounds by reduction. Such derivatives can be manufactured in symmetrical substituted amine groups (those derivatives with two or more amino or azido groups symmetrically disposed on the cyclodextrin molecule or as a symmetrically substituted amine or azide derivatized cyclodextrin molecule). Due to the nucleophilic displacement reaction that produces the nitrogen containing groups, the primary hydroxyl group at the 6-carbon atom is the most likely site for introduction of a nitrogen-containing group. Examples of nitrogen containing groups that can be useful in the invention include acetylamino groups (NHAc), alkylamino including methylamino, ethylamino, butylamino, isobutylamino, isopropylamino, hexylamino, and other alkylamino substituents. The amino or alkylamino substituents can further be reactive with other compounds that react with the nitrogen atom to further derivatize the amine group. Other possible nitrogen containing substituents include dialkylamino such as dimethylamino, diethylamino, piperidino and piperizino.

(21) The cyclodextrin molecule can be substituted with heterocyclic nuclei including pendent imidazole groups, histidine, imidazole groups, pyridino and substituted pyridino groups.

(22) Cyclodextrin Modified Polyvinyl Polymers

(23) The cyclodextrin can also be used as a part of a thermoplastic polymer. The cyclodextrin can be a pedant group or formed in the polymer backbone. Cyclodextrin-modified polymers including final polymers such as a polyolefin resin can be prepared by covalently grafting a cyclodextrin moiety onto a polyolefin or polyolefin blend. The grafting can be achieved by reacting a functional group, such as a hydroxyl group of cyclodextrin (CD) with a functional group, such as an epoxy acid, acid chloride or anhydride moiety, on the polymer or blend to form a bond between the cyclodextrin and the polyolefin. In another embodiment, an anhydride or epoxide component of the functionalized polymer can be used to form a reaction product. For example, a primary hydroxyl on the cyclodextrin reacts with an epoxy, acid chloride or a maleic anhydride moiety of the resin under conditions that convert substantially all anhydride groups to a half-ester.

(24) The modified polymers and the cyclodextrin grafted polymer compositions, according to the present disclosure, are useful in fibers, woven or non-woven fabrics, extruded or molded structures such as thin films, laminates, semi-rigid films and rigid containers. For instance, these structures provide functional properties for a flexible packaging structure, insert, closure or other packaging component. Polymers that can contain a cyclodextrin moiety in the backbone of the polymer can take a number of forms. The polymer can be a linear polymer having repeating units derived from the cyclodextrin structure. The polymer can have alternating residues derived from cyclodextrin and one or more other monomers, typically in a polycondensation format. Further, the polymer can take the form of a later polymer or a polymer formed by extensively crosslinking the cyclodextrin molecule into a highly crosslinked structure. Cyclodextrin can be crosslinked with 1-chloro-2,3epoxypropene to form a highly crosslinked cyclodextrin structure. A linear tube of cyclodextrins can be made by condensing the cyclodextrin in a linear tube wherein in the polymer structure, the cyclodextrin is formed as the rise of a ladder in a structural format. Linear and highly branched cyclodextrin polymers can be made by polycondensation of cyclodextrins with an epoxy compound such as ethylcholorohydrin to form a cyclodextrin ethylcholorohydrin copolymer. Linear compositions can be made by reacting cyclodextrin molecules with amino ethyls and then condensing with polycondensation reactants as shown in Hwang et al., Effects of Structure of -Cyclodextrin-Containing Polymers on Gene Delivery, Bioconjugate Chem., 2001, 12(2), pp. 280-290.

(25) Embodiments in accordance with the present disclosure also include a chip with a major dimension of less than about 10 mm and a weight of about 20 to 50 mg, whereby the chip comprises compositions of the present disclosure as described above. Further embodiments include a container comprising an enclosed volume surrounded by a polyolefin web, the web comprised of compositions as described above, such containers being useful, for example, in the packaging of food. Additionally, fibers and films prepared from the compositions of the present disclosure are also included in accordance with the present disclosure.

(26) The addition of maleic anhydride to a normal alpha olefin generates an alkenyl succinic anhydride. The ene reaction is an indirect substituting addition. It involves the reaction of an olefin with an allylic hydrogen (ene) with an enophile, e.g., maleic anhydride. The reaction results in a new bond forming between two unsaturated carbons and the allylic hydrogen transfers to the maleic anhydride through a cyclic transition state. The reaction can be carried out using a range of normal alpha olefins from 1-butene to C.sub.30+ normal alpha olefin wax. The maleic anhydride molecule supplies the reactive anhydride functionality to the alkenyl succinic anhydride, while the long chain alkyl portion provides the hydrophobic properties.

(27) ##STR00003##
Alkenyl succinic anhydride materials are available commercially such as maleic anhydride derivatives comprise products with an alkenyl backbone that starts at C.sub.8 and progresses through to C.sub.18. By changing the nature of the starting alkene (i.e. straight chain vs. isomerize form) the physic-chemical properties of the resultant alkenyl succinic anhydride (e.g. solid vs. liquid form at room temperature) can be modified. Commercially available useful materials include: dodecenylsuccinic anhydride, n-tetradecenyl succinic anhydride, hexadecenyl succinic anhydride, iso-hexadecenyl succinic anhydride, octadecenyl succinic anhydride, and tetrapropenyl succinic anhydride. The polymethylene chains are shown in a specific conformation for convenience purposes and do not conform to these structures in the composition of the invention.

(28) Hydrocarbyl-substituted succinic acids and anhydrides are preferred high-molecular weight carboxylic acids and anhydrides. These acids and anhydrides can be prepared by reacting maleic anhydride with an olefin or a chlorinated hydrocarbon such as a chlorinated polyolefin. The reaction involves merely heating the two reactants at a temperature in the range of about 100 C. to about 300 C., or about 100 C. to 200 C.

(29) The product from this reaction is a hydrocarbyl-substituted succinic anhydride wherein the substituent is derived from the olefin or chlorinated hydrocarbon. The product may be hydrogenated to remove all or a portion of any ethylenically unsaturated covalent linkages by standard hydrogenation procedures, if desired. The hydrocarbyl-substituted succinic anhydrides may be hydrolyzed by treatment with water or steam to the corresponding acid. The high-molecular weight hydrocarbyl-substituted succinic acids and anhydrides can be represented by the formula:

(30) ##STR00004##
Wherein R is the hydrocarbyl substituent. Preferably R contains from about 10 to about 500 carbon atoms, or from about 15 to about 500 carbon atoms, or from about 18 to about 500 carbon atoms.
Thermoplastic Resins

(31) Polyolefins such as polyethylene and polypropylene can be use in the invention as well as copolymers of ethylene propylene and other alpha olefin monomers.

(32) Commercial polyolefin functionalization is achieved using solution, melt and solid state routes known in the art. The process covalently bonds monomers onto vinyl polymers or onto polyolefin polymers including copolymers of olefins with other monomers, such as vinyl monomers. Polyolefins useful in modified or un-modified embodiments according to the disclosure include poly(ethylene) or PE, poly(propylene) or PP, poly(ethylene-co-propylene) or PEP, ethylene/methyl acrylate copolymer, and ethylene/ethyl acrylate copolymer. The polyolefins can be functionally modified with unsaturated compounds such as unsaturated anhydrides and carboxylic acids. Any packaging grade of a vinyl polymer can be used.

(33) Polyolefin and functionalized polyolefins have extensive industrial applications such as coextrusion tie resins in multi-layer films and bottles for the food industry, compatibilizers for engineering polymers and plastic fuel tank tie resins for the automotive industry, flexibilization and compatibilization of halogen free polymers for cables and for filler materials used in roofing construction. Functionalized polyolefins can also find application in containers for food contact. Functionalized polyolefins useful in the present disclosure are maleated polyethylene and polypropylene (OREVAC and LOTRYL available from Arkema, Philadelphia, Pa., PLEXAR resins available from EQUISTAR, Rotterdam, The Netherlands, ADMER resin from Mitsui Chemicals, Tokyo, Japan, FUSABOND resins from DuPont, Wilmington, Del., OPTIM resins from MNAS, India and EXXELOR from Exxon/Mobil, Houston, Tex.), functionalized EP, EVA and EPDM (such as ethylene-propylene-butadiene or, ethylene-propylene-1,4-hexadiene polymers) ethylene-octene copolymers, ethylene-n butyl acrylate-maleic anhydride, ethylene-ethylacrylate-maleic anhydride terpolymers and copolymers of ethylene-glycidyl methacrylate and the like. The ethylene-propylene-1,4-hexadiene copolymer can be represented as:

(34) ##STR00005##
wherein x is selected to obtain about 70 to 90 wt % ethylene, y is selected to obtain about 10 to 30 wt % propylene and z is selected to obtain up to about 5 wt % 1,4-hexadiene. The vacant bonds are linked to similar groups, H, or end groups.

(35) Other polyolefins which are known in the art can be used in compositions of the present invention to impart desirable processing or end product characteristics. For example, polybutene can be added to increase fiber strength. Other olefins that can be added to produce copolymers or blends include alpha olefins such as 1-hexene and 1-octene to impart flexibility.

(36) Compositions in accordance with the present disclosure can be prepared using reactive extrusion by feeding a dry cyclodextrin, or derivative thereof, (<0.10% moisture), a functionalized polyolefin and optionally a second polyolefin, into an extruder at temperatures such that the cyclodextrin reacts with the functionalized polyolefin as the molten polymer and cyclodextrin are transported through the extruder to form a reaction product containing, for example, an ester group which covalently bonds the cyclodextrin to the polyolefin. The ratio of functionalized polyolefin to non-functionalized polyolefin can be adjusted for a specific application and conversion process.

(37) The present invention is directed to a stoichiometric reaction product of a cyclodextrin (CD) and a graft linking agent (i.e., anhydride, epoxide, etc.), and a non-volatile and polymer compatible carboxylic acid, resulting in a modified polymer especially suited as a masterbatch which can be subsequently let down with one or more non-functionalized thermoplastic polymers and thermoplastic elastomers at a weight ratio of one (1) parts of the masterbatch composition to ten (10) to twenty (20) parts of non-functionalized polymer. A maleic acid, fumaric acid or maleic anhydride functionalized material is useful for bonding CD to the polyolefin. The stoichiometric ratio for melt grafting is calculated on a gram-mole (gram-formula-weight) basis where one (1) gram-mole of CD (, or form) is equivalent to one (1) gram-mole the grafted anhydride, glycidyl and carboxylic acid moiety.

(38) The structures of the invention can be made by coating a liquid containing the cyclodextrin compound and the complexed 1-MCP onto a substrate. The substrate to be coated can be in any form, such as a flexible film, web, nonwoven or woven material or foam. Any of the substrates mentioned above can be used but preferred substrates are films and fiber in the form of woven or non-woven fabric. The substrate can be porous or nonporous and can be made of materials such as plastic, paper or fabric from either natural or synthetic fiber.

(39) The coating composition can contain the grafted cyclodextrin or the substituted cyclodextrin in a coatable solution, dispersion or suspension. The coating can be made by combining coating materials in a liquid phase. Such liquids can contain aqueous materials or non-aqueous liquids or as an aqueous phase containing non-complexing, water-soluble co-solvents (e.g., glycol ethers). Aqueous coatings are preferred due to low costs and ease of manufacture. As discussed elsewhere the moisture content of the final coating is important for control of the 1-MCP release characteristics. Solvent coating can be made and have the advantage of not containing substantial quantities of water that require a drying step. Many solvents require shorter and cooler drying cycles.

(40) The coating can be made by dispersing or dissolving the coating constituents in the liquid phase and mixing until uniform. Such coating compositions contain a major portion of the liquid phase typically about 50 to 70 wt. % of liquid. The coating can contain about 0.5 to 20 wt % of the cyclodextrin, calculated as cyclodextrin in the form of the substituted cyclodextrin or the polymer grafted cyclodextrin. Depending on the amount of cyclodextrin in the cyclodextrin compound, the coating composition can contain about 5 to 40 wt. % of the cyclodextrin compound. The cyclodextrin is typically introduced into the coating composition in the form of small particulate or small particle dispersion. Such small particles can be formed prior to addition to the liquid phase but can also be formed mechanically after addition.

(41) Such coating compositions typically comprise vinyl polymers adapted for coating purposes. Such polymers are typically formulated into aqueous solutions that can also contain rapid drying solvent materials. Typical coating compositions comprise homopolymers, copolymers, terpolymers, etc. including acetate, acrylic, sytrenic, polysaccharides, acrylamide/acrylate copolymers, and carboxymethylcellulose and other polymer systems; adjuvants or excipients, such as a gelling agent, including naturally occurring compounds such as carrageenan and gelatin, extenders, binders, lubricants, surfactants and/or dispersants, wetting agents, spreading agents, dispersing agents, stickers, adhesives, defoamers, thickeners, emulsifying agents, inorganic agents such as calcium chloride, magnesium chloride, lithium chloride, zinc chloride, magnesium nitrate, and aluminum nitrate; and combinations and mixtures thereof.

(42) A typical aqueous coating formulation can contain the following:

(43) TABLE-US-00002 Water 40-80% Binder (EVA or SBA) 20-40% Pigment 0-40%

(44) Surfactants, Leveling Agents, Defoamers, Stabilizers

(45) A typical solvent based coating formulation can contain the following:

(46) TABLE-US-00003 Solvent 40-80% Co-Solvent 0-5% Binder (numerous polymers) 20-40% Pigment 0-40%

(47) Leveling Agents Stabilizers

(48) The term produce material is used in a generic sense herein, and includes live respiring and ethylene generating plant materials. Included are woody-stemmed plants such as trees and shrubs. Plants to be treated by the methods described herein include whole plants and any portions thereof, such as field crops, potted plants, cut flowers (stems and flowers), and harvested fruits and vegetables. These include any plant that matures or ripens due to the presence of or the generation of ethylene as a maturation hormone. The present invention can be employed to modify a variety of different ethylene responses. Ethylene responses may be initiated by either exogenous or endogenous sources of ethylene. Ethylene responses include, for example, the ripening and/or senescence of flowers, fruits and vegetables, abscission of foliage, flowers and fruit, the prolongation of the life of ornamentals such as potted plants, cut flowers, shrubbery, and dormant seedlings, in some plants (e.g., pea) the inhibition of growth, and in other plants (e.g., rice) the stimulation of growth. Additional ethylene responses or ethylene-type responses that may be inhibited by active compounds of the present invention include, but are not limited to, auxin activity, inhibition of terminal growth, control of apical dominance, increase in branching, increase in tillering, changing biochemical compositions of plants (such as increasing leaf area relative to stem area), abortion or inhibition of flowering and seed development, lodging effects, stimulation of seed germination and breaking of dormancy, and hormone or epinasty effects.

(49) Vegetables can be treated by the method of the present invention to inhibit ripening and/or senescence including leafy green vegetables such as lettuce, spinach and cabbage. Various roots are included such as potatoes and carrots. Plants from bulbs, such as tulips, shallots, onions; herbs, such as basil, oregano, dill; as well as soybean, lima bean, pea, corn, broccoli, cauliflower, and asparagus. Fruits include tomatoes, apples, bananas, pears, papaya, mangoes, peaches, apricots, nectarines; citrus including orange, lemon, lime, grapefruit, tangerines; other fruits such as kiwi; melons such as cantaloupe, musk melon, pineapple, persimmon; various small fruits including berries such as strawberries, blueberries and raspberries; green beans, cucumber and avocado. Ornamental plants that have ornamental character from flower, leaf, stem (bamboo) such as potted or cut flowers can be helped with the invention. Azalea, hydrangea, hibiscus, snapdragons, poinsettia, cactus, begonias, roses, tulips, daffodils, petunias, carnation, lily, gladiolus, alstroemeria, anemone, columbine, aralia, aster, bougainvillea, camellia, bellflower, cockscomb, chrysanthemum, clematis, cyclamen, freesia, and orchids are included. Plants that can be treated by the method of the present invention include cotton, apples, pears, cherries, pecans, grapes, olives, coffee, snapbeans and fig, as well as dormant seedlings such as various fruit trees including apple, ornamental plants, shrubbery, and tree seedlings. In addition, shrubbery can be treated by the method of the present invention including privet, photinea, holly, ferns, scheffiera, aglaonema, cotoneaster, barberry, waxmyrtle, abelia, acacia and bromeliades. Also included are living or respiring plants and plant material without edible or ornamental materials including shoots, planting stock, grafting stock, seeds, bulbs, planting eyes, flowers, etc.

(50) The following exemplary section contains examples of thermoplastic materials in the form of film and fiber and also contains data showing the properties of the thermoplastic material with respect to the use of the alternate inhibitor compound. In these data the compound 1-butene is used as a model compound. This compound is used since it is an inexpensive material that can mimic the properties of 1-MCP in both introducing the inhibitor material into the thermoplastic materials of the invention and can mimic the release properties of the material under use conditions.

(51) In the polymer materials of the invention the components can be used at the following levels depending on the formation of either a masterbatch or the final blended polymer material, the nature of the web and the produce contained.

Polymer Compositions

Based on the Masterbatch Material or the Final Blended Material

(52) TABLE-US-00004 Component Wt. % Wt. % Wt. % Inhibitor 0.0001 to 3 0.02 to 2 0.01 to 1 Cyclodextrin 0.2 to 20 0.3 to 10 0.5 to 7 CD-Grafted 1 to 65 2 to 50 5 to 45 polymer Polymer 1 to 90 1 to 80 5 to 70

Examples and Data

(53) Fiber Example 1:

(54) Spunbond Fiber produced on a 1 meter Reifenhauser spun-bonded fabric line having a basis weight of 21.4 gm/sq meter and 20 g fibers and having:

(55) 1.5% -cyclodextrin grafted onto the polyolefin blend (Cavamax W6A lot 60F203 manufactured by Wacker Chemie)

(56) 5.0% Fusabond 411D lot VR30087227 manufactured by DuPont

(57) 5.0% Fusabond 353D lot VR30091736 manufactured by DuPont

(58) 2.8% Poly B 0300M manufactured by Basell

(59) 86% polyolefin resin (Polypropylene 3155 manufactured by ExxonMobil)

(60) Control fiber example 1: SB Spunbond Fiber produced on a 1 meter Reifenhauser spunbond line having a basis weight of 21.4 gm-m.sup.2, 20 fibers.

(61) 100% polypropylene 3155 (ExxonMobil)

(62) Film Example 2:

(63) Three layer coextruded blown polyethylene film structure6 mil thickness.

(64) Outside sealant layers (2 mil each): 2% -cyclodextrin grafted onto the polyolefin (Cavamax W6A lot 60F203 manufactured by Wacker Chemie). 21.5% Integrate NE542-013 manufactured by Equistar. 38.2% Affinity PF1140G manufactured by Dow Plastics. 38.3% Exact 8852G manufactured by ExxonMobil.

(65) Core (2 mil): Mobil LGA 105 low density polyethylene.

(66) Film Example 2:

(67) Three layer coextruded blown polyethylene film structure6 mil thickness.

(68) Outside sealant layers (2 mil each): 2% -cyclodextrin grafted onto the polyolefin blend (Cavamax W6A lot 60F203 manufactured by Wacker Chemie). 50% Affinity PF1140G manufactured by Dow Plastics. 50% Exact 8852G manufactured by ExxonMobil.

(69) Core (2 mil): Mobil LGA 105 low density polyethylene

(70) Coating Example 1:

(71) TABLE-US-00005 Deionized Water 85.75% Airflex920 Emulsion (Air Products and 9.50% Chemicals, Inc; Allentown, PA18195) Pluronic 31R1 manufactured by BASF. 0.75% -cyclodextrin (Cavamax W6F 4.00% manufactured by Wacker Chemie)

Film and Spunbond Fiber Sample Production Procedure

(72) First sample set: Each of Film example 2 samples and control film example 2 samples were cut into 44 sheets.

(73) Second sample set: Spun-bond fiber example 1 samples and control fiber example 1 samples were cut into 8.38.3 sheets.

(74) The first set of film was found to have a moisture content of 0.13%. The film was previously stored in a storage room at 20 C. and 50% humidity for greater than 6 weeks.

(75) The first set of fiber was found to have a moisture content of 0.17%. The fiber was stored in uncontrolled temperature and humidity warehouse space for greater than 6 weeks.

(76) The second set of samples was placed in a vacuum oven to dry. The vacuum was held at greater than 0.1 mm-Hg for a period of 24 hours at a temperature of 100 C. for the fiber and 60 C. for the films. The dried samples of film and fiber had a moisture content of <0.08%.

(77) For both the first sample set and second sample set, 75 of the each of the four kinds of sheets were placed in separate 3 liter Tedlar gas sample bags. The Tedlar bags, which were cut open to insert the sheets, were then resealed using a direct heat sealer after the sheets were in place. Once sealed all remaining air trapped in the Tedlar bags was withdrawn with a glass syringe via the stainless steel fittings incorporated into the bags. The evacuated bags were then injected with 150 mL of 99.0% 1-butene gas. The 1-butene was used as a surrogate for 1-MCP since both compounds have ethylene generating inhibitory capacity, have similar molecular size, four carbon atoms and one olefinic bond.

(78) In the case of the bag with the Film example 2 samples, this amount of the gas translates to a 1-butene to -CD molar ratio of 4.5:1. In the case of the bag with the fiber example 1 samples, this amount of the gas translates to a 1-butene to -CD molar ratio of 5.9:1. Oversaturation of 1-butene is desired to encourage complexation. The Tedlar bags and their contents were then placed in a 5 L pressure vessel. The pressure vessel was pressurized by the introduction of nitrogen to 1205 psig at 20 C. The vessel was held at this pressure and temperature for a period of 24 hours. After 24 hours of pressurization, the Tedlar bags were removed from the vessel; the sheets were removed from the bags and exposed to ambient conditions (20 C. and 50% RH) for amounts of time ranging from one hour to one week.

Sample Production Procedure for Coated Meltblown Fiber

(79) Samples of meltblown (MB) fiber which contained no CD were cut into 66 sheets. These sheets were coated with either a CD containing coating or a control coating that had zero CD content. Both coatings were 85.76% water, 9.52% Airflex 920 Emulsion, and 0.75% Pluronic surfactant. The Airflex 920 Emulsion is 55% solids and contains vinyl acetate polymers, water and 7732-18-5 biocide. The Pluronic is specifically made up of the tri-block copolymer poly(propylene glycol)-block-poly(ethylene glycol)-block-poly(propylene glycol) and has an HLB (hydrophile-lipophile balance) of 1. The CD containing coating had a 4.00% alpha cyclodextrin content. The control coating had a 4.00% D-(+)-maltose monohydrate content.

(80) The coatings were applied to the fiber until the fiber sample was completely wetted out. Immediately after the coating was applied, the samples were hung to dry in ambient conditions. The fiber samples were inverted periodically so that the coating dried evenly across the surface of the fiber. Once dry to the touch, the fiber samples were placed in the vacuum oven to dry. The vacuum was held at <0.1 mmHg for a period of 24 hours at a temperature of 100 C. The dried samples of fiber had a moisture content of <0.18%.

(81) 50 of the control and CD coated meltblown fiber sheets were then placed in two separate Tedlar bags. The Tedlar bags, which were cut open to insert the sheets, were then resealed using a direct heat sealer after the sheets were in place. Once sealed, all of the remaining air trapped in the Tedlar bags was withdrawn with a glass syringe via the stainless steel fittings that are attached to the bags. The evacuated bags were then injected with 100 mL of 99.0% 1-butene gas. This amount of the gas translates to a 1-butene to -CD molar ratio of 4.5:1. The Tedlar bags and their contents were then placed in a 5 L pressure vessel. The pressure vessel was pressurized with nitrogen to 1205 psig. The vessel was held at this pressure for a period of 24 hours. After pressurization, the Tedlar bags were removed from the vessel; the sheets were removed from the bags and exposed to ambient atmosphere conditions (20 C. and 50% RH) for 24 and 48 hours prior to analysis.

(82) Analytical Test Method

(83) The static adsorption test method is most easily explained in terms of a test substrate (a sheet of film or fiber) surrounded by a fixed volume (e.g., a volume held within sealed glass bottle). Test substrate and volume were initially free of the test solute (1-butene inhibitor) inside the close-volume bottle. At time zero, a specific weight of the test substrate was placed inside the sealed glass bottle (250 mL serum bottle with Teflon faced silicone screw cap seal). Headspace concentrations of 1-butene were measured at different time intervals following introduction of test substrate into bottle. The 1-butene headspace concentration surrounding the test structure was quantified using gas chromatography.

(84) A gas chromatograph (HP 5890) operated with flame ionization detection (FID), a six-port heated sampling valve with 1 mL sampling loop and data collection software (HP ChemStation A06.03-509) was used to measure the 1-butene headspace concentration. Static headspace concentration was determined in test samples using a five point 1-butene calibration curve measured in L of 1-butene per 250 mL bottle volume and presented as L/L or parts per million (vol./vol.).

(85) Test substrates were placed into a 250 mL serum bottle with Teflon faced silicone septa. The serum bottle was maintained at room temperature (20 C.) during the test interval. At each sampling interval, the serum bottle headspace was sampled by removing 1 mL of gas from the sample bottle using a Valco Instrument six port manual gas sampling valve (Valco #DC6WE) interface directly to the GC column.

(86) HP 5890 GC

(87) Zone Temperatures:

(88) TABLE-US-00006 Setpoint Six port valve 120 C. Detector (FID) 150 C. Over Zone: Equib Time 0.00 min.
Oven Program:

(89) TABLE-US-00007 Setpoint Isothermal Temp.: 150 C. Initial Time: 1.20 min. Runtime (min): 1.20 min.

(90) The 1-butene working standard was prepared by diluting 10 mL of 99.0% pure 1-butene gas (Scotty Gas #BUTENE01) in a Tedlar gas sampling bag containing 1 liter of air. The 1-butene working standard concentration was 10,226 L/L (PPM).

(91) Calibration standards were prepared at five concentration levels by injecting via a 250 L gas tight syringe (Hamilton Gastight #1725) 50, 100, 200, 300 and 400 L of the working standard into 250 mL the serum bottles fitted with Teflon faced silicone septa. ChemStation software was used to calculate a 1-butene response factor using a linear regression equation. The 1-butene standard curve correlation coefficient was 0.999.

(92) The test substrate was placed into a 250 mL serum bottle and left alone for one hour at room temperature conditions (20 C.). After this one hour period the headspace was analyzed to obtain a precise 1-butene headspace concentration. The headspace was analyzed by GC/FID. Parenthetically, little or no desorption from the test substrate took place in the first hour because of the lack of humidity in the headspace of the jar.

(93) After the initial headspace sample was taken, 50 L of deionized water was injected into the jar to create a 100% humid atmosphere inside the jar. Care was taken so that the liquid water did not come in direct contact with the film or fiber sample. The water vapor in the volume equilibrated throughout the volume. One hour after injection of the water a second headspace sample was analyzed. A final headspace sample was analyzed 24 hours after the injection of water. Samples are analyzed in quadruplicate and values averaged. Desorption is determined by the difference from the initially measured 1-butene concentration at 1 hour and the later headspace sampling times.

(94) 1-Butene Desorption Data with and without Humidification for Spunbond (SB) Fiber Samples as a Function of Atmospheric Exposure

(95) TABLE-US-00008 TABLE 1 SB Fiber SB Fiber SB Control SB Control SB Fiber Example 1 Example 1 Atmospheric SB Control Humidified Humidified Example 1 Humidified Humidified Exposure Dry 1 hr 24 hr Dry 1 hr 24 hr Time (hr) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) 1 3.36 4.07 5.63 24.32 32.12 37.71 4 0.70 0.77 1.92 1.89 5.96 10.24 6 0.24 0.39 1.42 0.78 4.00 8.05 24 0.32 0.33 0.74 0.74 3.02 5.93 48 0.00 0.19 0.49 0.19 2.09 3.39 72 0.00 0.10 0.70 0.16 1.77 2.98 144 0.00 0.20 0.16 0.00 1.41 1.86 Note: SB fiber dried immediately prior to 1-Butene pressurization.

(96) These data show the average amount of 1-butene in the headspace of 250 mL jars containing sheets of SB fiber that are dry, humidified 1 hour, and humidified 24 hours. The fiber sheets have been exposed to the atmosphere (20 C. and 50% RH) for varying lengths of time after pressurized exposure to 1-butene. Moisture content of samples was <0.08% prior to 1-butene pressurization. In the humidified samples of the invention the release of the 1-butene model compound was achieved through 144 hours or 6 days. In sharp contrast to the control samples containing no inhibitor and the dry samples, both failed to maintain an effective release in comparison to the examples of the invention.

(97) 1-Butene Desorption Data with and without Humidification for Film Samples as a Function of Atmospheric Exposure

(98) TABLE-US-00009 TABLE 2 Film Film Control Film Control Film Film Example 2 Example 2 Atmospheric Control Film Humidified Humidified Example 2 Humidified Humidified Exposure Dry 1 hr 24 hr Dry 1 hr 24 hr Time (hr) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) 1 2.43 2.42 2.53 19.48 28.72 29.62 4 0.27 0.19 0.35 1.14 8.99 10.14 6 0.00 0.15 0.25 0.59 7.44 9.07 24 0.00 0.11 0.14 0.59 5.28 6.35 48 0.00 0.07 0.16 0.08 3.69 4.59 72 0.00 0.03 0.16 0.15 3.11 3.63 144 0.00 0.00 0.00 0.00 2.13 2.19 Note: Film vacuum dried immediately prior to 1-Butene pressurization.

(99) These data show the average amount of 1-butene in the headspace of 250 mL jars containing sheets of film that are dry, humidified 1 hour, and humidified 24 hours. The film sheets have been exposed to the atmosphere (20 C. and 50% RH) for varying lengths of time after pressurized exposure to 1-butene. Moisture content of samples was <0.08% prior to 1-butene pressurization. In the humidified samples of the invention the release of the 1-butene model compound was achieved through 144 hours or 6 days. In sharp contrast to the control samples containing no inhibitor and the dry samples, both failed to maintain an effective release in comparison to the examples of the invention.

(100) 1 Butene Desorption Data with and without Humidification for Spunbond (SB) Fiber Stored in Uncontrolled Atmosphere for Six Weeks as a Function of Atmospheric Exposure

(101) TABLE-US-00010 TABLE 3 SB Fiber SB Fiber Control SB Control SB SB Fiber Example 1 Example 1 Atmospheric Control SB Humidified Humidified Example 1 Humidified Humidified Exposure Dry 1 hr 24 hr Dry 1 hr 24 hr Time (hr) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) 4 3.68 4.98 8.90 5.70 8.21 13.99 24 0.25 0.31 0.39 0.28 0.32 0.11 48 0.25 0.13 N/A 0.20 0.12 N/A

(102) These data show the average amount of 1-butene in the headspace of 250 mL jars that contain sheets of SB fiber that are dry, humidified 1 hour, and humidified 24 hours. The fiber sheets have been exposed to the atmosphere (20 C. and 50% RH) for varying lengths of time after pressurized exposure to 1-butene. Moisture content of samples was 0.17% prior to 1-butene pressurization.

(103) 1-Butene Desorption Data with and without Humidification for Film Stored in a Controlled Atmosphere of 50% Humidity for Six Weeks as a Function of Atmospheric Exposure

(104) TABLE-US-00011 TABLE 4 Film Film Control Film Control Film Film Example 2 Example 2 Atmospheric Control Film Humidified Humidified Example 2 Humidified Humidified Exposure Dry 1 hr 24 hr Dry 1 hr 24 hr Time (hr) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) 24 0.17 0.09 0.21 0.34 5.01 5.57 96 0.35 0.27 0.29 0.33 4.55 6.22 144 0.64 0.35 0.38 1.03 3.54 4.83 288 0.00 0.00 0.07 0.00 2.99 3.73

(105) These data show the average amount of 1-butene in the headspace of 250 mL jars that contain sheets of film that are dry, humidified 1 hour, and humidified 24 hours. The film sheets have been exposed to the atmosphere (20 C. and 50% RH) for varying lengths of time after pressurized exposure to 1-butene. Moisture content of samples was 0.13% prior to 1-butene pressurization. In the humidified samples of the invention the release of the 1-butene model compound was achieved through 288 hours or 12 days. In sharp contrast to the control samples containing no inhibitor and the dry samples, both failed to maintain an effective release in comparison to the examples of the invention

(106) 1-Butene Desorption Comparison of SB Fiber with 1-Butene complexed at 120 psig and 0 psig as a function of Atmospheric Exposure Time.

(107) TABLE-US-00012 TABLE 5 SB Fiber SB Fiber SB Fiber SB Fiber Atmospheric Example 1 Example 1 Example 1 Example 1 Exposure 120 psig, 6 hr 120 psig, 24 hr 0 psig, 24 hr 0 psig, 48 hr Time (hr) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) 1 3.02 0.39 0.51 24 5.93 0.78 0.74

(108) These data show the average amount of 1-butene in the headspace of 250 mL jars that contain fiber exposed to 1-butene at 120 psig for 6 hours and 24 hours, fiber exposed to 1-butene at 0 psig for 24 hours and 48 hours. In each case 75 sheets of 8.38.3 inch fiber webs per 3 Liter Tedlar bag with 150 ml of 1-butene gas at STP. Moisture content of fiber was <0.17% prior to complexation. The materials made at higher pressure released a greater amount of inhibitor.

(109) 1-Butene Desorption Comparison of Film with 1-Butene Complexed at 120 psig and 0 psig as a Function of Atmospheric Exposure Time.

(110) TABLE-US-00013 TABLE 6 Atmospheric Film Ex. 2 Film Ex. 2 Film Ex. 2 Film Ex. 2 Exposure 120 psig, 6 hr 120 psig, 24 hr 0 psig, 24 hr 0 psig, 48 hr Time (hr) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) 1 5.28 1.02 1.64 24 6.35 1.25 2.05

(111) These data show the average amount of 1-butene in the headspace of 250 mL jars that contain film exposed to 1-butene at 120 psig for 6 hours and 24 hours, film exposed to 1-butene at 0 psig for 24 hours and 48 hours. In each case 75 sheets of 4.04.0 inch films per 3 liter Tedlar bag with 150 ml of 1-butene gas at STP. Moisture content of film was <0.13% prior to complexation. The materials made at higher pressure released a greater amount of inhibitor.

(112) 1-Butene Desorption Data with and without Humidification for Coated Meltblown (MB) Fiber Samples as a Function of Atmospheric Exposure

(113) TABLE-US-00014 TABLE 7 Ctrl Coated Ctrl Coated CD Coated CD Coated Atmospheric Ctrl Coated MB Humidified MB Humidified CD Coated MB Humidified MB Humidified Exposure MB Dry 1 hr 24 hr MB Dry 1 hr 24 hr Time (hr) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) (ppm 1-butene) 24 0.39 0.58 1.02 0.58 4.08 11.8 48 0.09 0.17 0.72 0.23 2.06 8.45

(114) These data show the average amount of 1-butene in the headspace of 250 mL jars containing sheets of coated meltblown fiber that are dry, humidified 1 hour, and humidified 24 hours. The fiber sheets have been exposed to the atmosphere for 24 and 48 hours after pressurized exposure to 1-butene. Moisture content of samples was <0.18% prior to 1-butene pressurization for 24 hours. In the humidified samples of the invention coated MB samples the release of the 1-butene was greater than achieved with either spunbond fiber or film for the same period of atmospheric exposure time of 24 and 48 hours of atmospheric exposure of 20 C. and 50% relative humidity (RH). In sharp contrast to the control samples containing no inhibitor and the dry samples, both failed to maintain an effective release in comparison to the coated meltblown examples of the invention.

(115) In summary, these data show that a humidified enclosed space containing the composition of the invention can lead to the release of an effective quantity of the olefinic inhibitor compound for an extended period of time up to twelve days of atmospheric exposure of 20 C. and 50% RH. The data further shows that the data support the effective release of complexed olefinic compound from film, fiber and coated fiber at high relative humidity achieved during storage of produce.

(116) Film Description

(117) Film Example 3

(118) Tri-layer, Co-Ex Emil blown film

(119) Outer layers: each layer 2 mil comprising:

(120) 2.0% -cyclodextrin Cavamax W6A lot 60F203 grafted onto the polyolefin blend (Wacker Chemie)

(121) 21.5% Integrate NE542-013

(122) 38.2% Affinity PF1140G (Dow Plastics)

(123) 38.3% Affinity 8852G (Dow Plastics)

(124) Core: 2 mil Mobil LGA 105 LDPE
Procedure for Extracting 1-MCP Gas and Sample Preparation
The 1-methylcyclopropene (1-MCP) was received in the form of a complex with cyclodextrin powder. The powder was estimated to contain 5 wt % 1-MCP. To extract the 1-MCP, 500 g of the powder was placed in a 3 L Tedlar bag along with a pouch containing 50 mL of D.I. water. The bag was sealed and the lab air was evacuated from it. Once sealed and evacuated, the pouch of water was popped, putting the water in contact with the powder. Gaseous 1-MCP is produced from the CD/1-MCP complex when exposed to high humidity. After a period of time, the bag filled with 1-MCP gas. 150 mL gaseous 1-MCP was then extracted from the bag via syringe and injected into another sealed and evacuated 3 L Tedlar bag that contained 75 sheets of film. This bag was then placed in a pressure vessel. The vessel was pressurized to 1205 psig. The vessel was held at this pressure for 40 hours. After this period, the films were removed from the vessel and bag and set out in either a controlled laboratory atmosphere (20 C., 50% RH) or a desiccator.
Testing Procedure

(125) 1. Film exposed to lab atmosphere or stored in a desiccator6, 24, 168 hours.

(126) 2. One film sample per 250 ml jar

(127) 3. Jar headspace sampled when dry, humidified 1 hr, and humidified 24 hr

(128) After being stored in either the lab atmosphere or desiccator for the desired amount of time, one film sample was placed in a 250 mL jar. The jar was allowed to sit for 1 hour at 20 C. Then, a 1 mL aliquot of the jar headspace was put onto a fused silica PLOT column. After this headspace sample was taken, 50 L of deionized water was injected into the jar to create a 100% humid atmosphere in side the jar. Care was taken so that the water did come in direct contact with the sample. One hour after injection of the water a second headspace sample was analyzed. A final headspace sample was analyzed 24 hours after the injection of water. The gas chromatographs generated were used to determine the 1-MCP content in the jar.

(129) Data for Film Pressurized with 1-MCP

(130) TABLE-US-00015 TABLE 1 The average amount of 1-MCP in the headspace of 250 mL jars that contain film sheets of 1-MCP pressurized Example 2 film that is dry, humidified 1 hour, and humidified 24 hours. The moisture content of the film was <0.08% prior to 1-MCP pressurization. Ex. 2 Ex. 2 Ex. 2 Ex. 2 Ex. 2 Desiccator Desiccator Ex. 2 Lab Exposed Lab Exposed Desiccator Exposed Exposed Exposure Lab Exposed Humidified Humidified Exposed Humidified Humidified Time Dry 1 hr 24 hr Dry 1 hr 24 hr (hr) (ppm 1-MCP) (ppm 1-MCP) (ppm 1-MCP) (ppm 1-MCP) (ppm 1-MCP) (ppm 1-MCP) 6 0.00 0.97 1.02 0.00 1.20 1.23 24 0.00 0.93 0.94 0.00 1.13 1.11 168 0.00 0.97 1.00 0.00 1.35 1.23

(131) The data further show the importance of using dry thermoplastic and coating materials to introduce the inhibitor compound into the interior of the central pore of a cyclodextrin compound at increased pressure.

(132) The foregoing discloses embodiments of the invention. In the Specification and claims, about modifying, for example, the quantity of an ingredient in a composition, concentration, volume, process temperature, process time, yield, flow rate, pressure, and like values, and ranges thereof, employed in describing the embodiments of the disclosure, refers to variation in the numerical quantity that can occur, for example, through typical measuring and handling procedures used for making compounds, compositions, concentrates or use formulations; through inadvertent error in these procedures; through differences in the manufacture, source, or purity of starting materials or ingredients used to carry out the methods, and like proximate considerations. The term about also encompasses amounts that differ due to aging of a formulation with a particular initial concentration or mixture, and amounts that differ due to mixing or processing a formulation with a particular initial concentration or mixture. Where modified by the term about the claims appended hereto include equivalents to these quantities. Optional or optionally means that the subsequently described event or circumstance may but need not occur, and that the description includes instances where the event or circumstance occurs and instances in which it does not. The present invention may suitably comprise, consist of, or consist essentially of, any of the disclosed or recited elements. Thus, the invention illustratively disclosed herein can be suitably practiced in the absence of any element which is not specifically disclosed herein. The use of the singular typically includes and at least does not exclude the plural.

(133) The specification, figures, examples and data provide a detailed explanation of the invention as it has been developed to date. The invention, however, can take the form of nonwovens, fibers, films, sheets, bottles, caps, and other embodiments without departing from the spirit or the intended scope of the invention. The invention therefore resides in the appended claims.