Container and composition for enhanced gas barrier properties
US-9051116-B2 · Jun 9, 2015 · US
US9464184B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9464184-B2 |
| Application number | US-201514704408-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 5, 2015 |
| Priority date | Dec 9, 2008 |
| Publication date | Oct 11, 2016 |
| Grant date | Oct 11, 2016 |
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A container comprising a polyester composition with enhanced carbon dioxide and oxygen barrier properties and methods of improving the gas barrier properties of polyester containers are provided. The polyester composition comprises a polyester and a gas barrier enhancing additive. In a particular embodiment, the gas barrier enhancing additive comprises a compound having the chemical formula: X—(X 1 ) s —COO—(X 2 ) t —X 3 —(X 4 ) u —OOC—(X 5 ) v —X 6 or X—(X 1 ) s —OOC—(X 2 ) t —X 3 —(X 4 ) u —COO—(X 5 ) v —X 6 .
Opening claim text (preview).
We claim: 1. A method for enhancing the mechanical properties of a polyester container, the method comprising: blending a polyester with at least one gas barrier additive to form a polyester composition having an I.V. from about 0.65 dL/g to about 1.0 dL/g; and stretch blow molding the polyester composition into a polyester container; wherein the at least one gas barrier additive comprises a compound having the chemical structure of Formula I: wherein X and X 6 , independent of one another, comprise hydrogen, halide, heteroatom, amino, amido, alkylamino, arylamino, alkoxy, aryloxy, nitro, acyl, cyano, sulfo, sulfato, mercapto, imino, sulfonyl, sulfenyl, sulfinyl, sulfamoyl, phosphonyl, phosphinyl, phosphoryl, phosphino, thioester, thioether, anhydride, oximno, hydrazino, carbamyl, phosphonic acid, phosphonato, or a C 1 -C 10 monovalent hydrocarbon which is unsubstituted or substituted with one or more functional moieties; wherein X 1 , X 2 , X 3 , X 4 , and X 5 , independent of one another, comprise a heteroatom or a C 1 -C 10 divalent hydrocarbon, wherein each heteroatom or C 1 -C 10 divalent hydrocarbon is unsubstituted or substituted with one or more functional moieties or one or more C 1 -C 10 hydrocarbyls that are unsubstituted or substituted with one or more functional moieties; wherein s, t, u, and v, independent of one another, is a number from 0 to 10; and wherein when X 3 comprises a C 6 or C 10 divalent aromatic hydrocarbon, X and X 6 , independent of one another, comprise a hydrogen, halide, heteroatom, hydroxyl, amino, amido, alkylamino, arylamino, alkoxy, aryloxy, nitro, acyl, cyano, sulfo, sulfato, mercapto, imino, sulfonyl, sulfenyl, sulfinyl, sulfamoyl, phosphonyl, phosphinyl, phosphoryl, phosphino, thioester, thioether, anhydride, oximno, hydrazino, carbamyl, phosphonic acid, phosphonato, or a C 3 -C 10 monovalent cyclic or heterocyclic non-aryl hydrocarbon that are unsubstituted or substituted with one or more functional moieties. 2. The method according to claim 1 , wherein the gas barrier additive comprises a compound having the chemical structure of Formula I, wherein X and X 6 each comprise a phenyl group, a naphthyl group, or a cyclohexyl group. 3. The method according to claim 1 , wherein the gas barrier additive comprises a compound having one of the following chemical structures according to Formula I: 4. The method according to claim 1 , wherein the gas barrier additive is present in the polyester composition in an amount in the range of about 0.1 to about 10 weight percent of the polyester composition. 5. The method according to claim 1 , wherein the polyester comprises polyethylene terephthalate. 6. The method according to claim 1 , wherein the polyester composition comprises a poly(ethylene terephthalate) based copolymer having less than 20 percent diacid, less than 10 percent glycol modification, or both, based on 100 mole percent diacid component and 100 mole percent diol component. 7. The method according to claim 1 , wherein the polyester composition comprises a polyester made using at least one first polycondensation catalyst selected from the group consisting of metals in groups 3, 4, 13, and 14 of the Periodic Table and comprising a catalyst residue remaining in the polyester from formation of the polyester, the catalyst residue comprising at least a portion of the at least one first polycondensation catalyst. 8. The method according to claim 1 , wherein the gas barrier additive comprises a compound having the chemical structure of Formula I, wherein X and X 6 , independent of one another, comprise a methyl, ethyl, phenyl, naphthyl, benzoate, hydroxyl, amino, amido, alkylamino, arylamino, alkoxy, aryloxy, or a monovalent C 3 -C 5 aliphatic cyclic group; wherein X 1 , X 2 , X 4 , and X 5 , independent of one another, comprise a divalent benzoate or C 1 -C 2 aliphatic group; wherein s and v, independent of one another, is a number from 0 to 2; wherein t and u, independent of one another, is a number from 1 to 2; and wherein X 3 comprises a divalent methyl, ethyl, phenyl, naphthyl, anthracenyl, a C 3 -C 5 aliphatic cyclic group, a C 3 -C 5 cyclic group with one or more heteroatoms, or a C 6 bi-furan. 9. The method according to claim 1 , further comprising a creep control agent, wherein the creep control agent comprises a compound having the chemical structure: wherein R 1 , R 2 , R 3 , and R 4 , independent of one another, may comprise a heteroatom, a tetravalent carbon atom, or a C 1 -C 3 divalent or trivalent hydrocarbon; wherein each heteroatom, tetravalent carbon atom, or C 1 -C 3 divalent or trivalent hydrocarbon may be unsubstituted or substituted with one or more functional moieties or one or more C 1 -C 10 hydrocarbyls that may be unsubstituted or substituted with one or more functional moieties; wherein i, ii, iii, iv, v, and vi, independent of one another, comprise a single, double, or triple bond; wherein when i is a double bond, ii and vi are single bonds; wherein when ii is a double bond, i and iii are single bonds; wherein when iii is a double bond, ii and iv are single bonds; wherein when iv is a double bond iii and v are single bonds; wherein when v is a double bond, iv and vi are single bonds; wherein when vi is a double bond, i and v are single bonds; wherein vii may be a single bond, double bond, or no bond at all connects R 3 and R 4 ; wherein m, n, o, and p, independent of one another, may be 0 or 1; wherein when m is 0, bonds ii and iii form a single continuous bond; wherein when n is 0, bonds vi and v form a single continuous bond; wherein when o is 0, R 4 is bonded to R 1 by a single bond; and wherein when p is 0, R 3 is bonded to R 2 by a single bond. 10. The method according to claim 1 , further comprising a creep control agent, wherein the creep control agent comprises a compound having the chemical structure: wherein A 1 , A 2 , R 8 , R 9 , and R 10 , independent of one another, may comprise a heteroatom, a tetravalent carbon atom, a C 1 -C 10 divalent or trivalent hydrocarbon, or a C 1 -C 10 hydrocarbyl that may be unsubstituted or substituted with one or more functional moieties; wherein each heteroatom, tetravalent carbon atom, or C 1 -C 10 divalent or trivalent hydrocarbon may be unsubstituted or substituted with one or more functional moieties or one or more C 1 -C 10 hydrocarbyls that may be unsubstituted or substituted with one or more functional moieties; wherein m′, n′, and p′, independent of one another, may be 0 or 1; wherein i, ii, and iii, independent of one another may be a single bond or a double bond; wherein t, u, v, and w, independent of one another may be a single bond, double bond, or triple bond; and wherein q, r, and s may be from 0 to 10,000. 11. The method according to claim 1 , further comprising a creep control agent, wherein the creep control agent comprises a compound having one of the following chemical structures: 12. The method according to claim 1 , further comprising a creep control agent, wherein the gas barrier additive comprises
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