MXPA00001929A - Biodegradable lactone copolymers - Google Patents
Biodegradable lactone copolymersInfo
- Publication number
- MXPA00001929A MXPA00001929A MXPA/A/2000/001929A MXPA00001929A MXPA00001929A MX PA00001929 A MXPA00001929 A MX PA00001929A MX PA00001929 A MXPA00001929 A MX PA00001929A MX PA00001929 A MXPA00001929 A MX PA00001929A
- Authority
- MX
- Mexico
- Prior art keywords
- monomer
- copolymer
- film
- copolymers
- polymer
- Prior art date
Links
- 229920001577 copolymer Polymers 0.000 title claims abstract description 93
- 238000006065 biodegradation reaction Methods 0.000 title claims abstract description 11
- 239000000178 monomer Substances 0.000 claims abstract description 75
- 150000002596 lactones Chemical class 0.000 claims abstract description 17
- 238000002425 crystallisation Methods 0.000 claims abstract description 15
- 230000005712 crystallization Effects 0.000 claims abstract description 15
- 229920000642 polymer Polymers 0.000 claims description 79
- -1 adipate ester Chemical class 0.000 claims description 33
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 19
- 238000006116 polymerization reaction Methods 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 15
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical group [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims description 14
- 241000424123 Trachinotus baillonii Species 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- KLCNVOLAHCGRPP-UHFFFAOYSA-N 3-tert-butyloxepan-2-one Chemical compound CC(C)(C)C1CCCCOC1=O KLCNVOLAHCGRPP-UHFFFAOYSA-N 0.000 claims description 4
- 229920001730 Moisture cure polyurethane Polymers 0.000 claims description 4
- ZNLAHAOCFKBYRH-UHFFFAOYSA-N 1,4-dioxane-2,3-dione Chemical class O=C1OCCOC1=O ZNLAHAOCFKBYRH-UHFFFAOYSA-N 0.000 claims description 2
- 125000003180 beta-lactone group Chemical group 0.000 claims description 2
- 125000000457 gamma-lactone group Chemical group 0.000 claims description 2
- 230000000379 polymerizing Effects 0.000 claims description 2
- 239000001294 propane Substances 0.000 claims description 2
- 239000010813 municipal solid waste Substances 0.000 abstract description 6
- 230000001629 suppression Effects 0.000 abstract description 2
- 238000009877 rendering Methods 0.000 abstract 1
- DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical compound CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 description 25
- 238000006243 chemical reaction Methods 0.000 description 20
- 238000002360 preparation method Methods 0.000 description 17
- 239000003054 catalyst Substances 0.000 description 15
- 239000002253 acid Substances 0.000 description 12
- 229920005862 polyol Polymers 0.000 description 11
- WNLRTRBMVRJNCN-UHFFFAOYSA-N Adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 9
- 238000000113 differential scanning calorimetry Methods 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 229910001868 water Inorganic materials 0.000 description 9
- 125000004122 cyclic group Chemical group 0.000 description 8
- 238000007792 addition Methods 0.000 description 7
- 238000009833 condensation Methods 0.000 description 7
- 230000005494 condensation Effects 0.000 description 7
- 150000002009 diols Chemical class 0.000 description 7
- 230000004927 fusion Effects 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- 239000003999 initiator Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 230000035939 shock Effects 0.000 description 7
- PWAXUOGZOSVGBO-UHFFFAOYSA-N Adipoyl chloride Chemical compound ClC(=O)CCCCC(Cl)=O PWAXUOGZOSVGBO-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 6
- 150000001991 dicarboxylic acids Chemical class 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 150000003077 polyols Chemical class 0.000 description 6
- 239000001361 adipic acid Substances 0.000 description 5
- 235000011037 adipic acid Nutrition 0.000 description 5
- 150000001408 amides Chemical class 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 5
- 229920001519 homopolymer Polymers 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 4
- JFCQEDHGNNZCLN-UHFFFAOYSA-N Glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 4
- 210000001138 Tears Anatomy 0.000 description 4
- 229920002988 biodegradable polymer Polymers 0.000 description 4
- 239000004621 biodegradable polymer Substances 0.000 description 4
- PTIXVVCRANICNC-UHFFFAOYSA-N butane-1,1-diol;hexanedioic acid Chemical compound CCCC(O)O.OC(=O)CCCCC(O)=O PTIXVVCRANICNC-UHFFFAOYSA-N 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
- XXMIOPMDWAUFGU-UHFFFAOYSA-N 1,6-Hexanediol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000002361 compost Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000005755 formation reaction Methods 0.000 description 3
- 150000004676 glycans Polymers 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 229920001282 polysaccharide Polymers 0.000 description 3
- 239000005017 polysaccharide Substances 0.000 description 3
- 150000004804 polysaccharides Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000007655 standard test method Methods 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-Butanediol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K 2qpq Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 2
- CHXLFXLPKLZALY-UHFFFAOYSA-N 4-methyloxepan-2-one Chemical compound CC1CCCOC(=O)C1 CHXLFXLPKLZALY-UHFFFAOYSA-N 0.000 description 2
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N Caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229940117969 NEOPENTYL GLYCOL Drugs 0.000 description 2
- 239000004698 Polyethylene (PE) Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N Sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N Suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- IGWHDMPTQKSDTL-JXOAFFINSA-N [(2R,3S,4R,5R)-3,4-dihydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl dihydrogen phosphate Chemical compound O=C1NC(=O)C(C)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(O)=O)O1 IGWHDMPTQKSDTL-JXOAFFINSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229920003232 aliphatic polyester Polymers 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 229920000704 biodegradable plastic Polymers 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000004059 degradation Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 150000003951 lactams Chemical class 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- 239000004707 linear low-density polyethylene Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920001610 polycaprolactone Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000000518 rheometry Methods 0.000 description 2
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 2
- 238000007142 ring opening reaction Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000001384 succinic acid Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 229940113165 trimethylolpropane Drugs 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- OXDXXMDEEFOVHR-CLFAGFIQSA-N (Z)-N-[2-[[(Z)-octadec-9-enoyl]amino]ethyl]octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCCNC(=O)CCCCCCC\C=C/CCCCCCCC OXDXXMDEEFOVHR-CLFAGFIQSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- 150000000180 1,2-diols Chemical class 0.000 description 1
- BTOOAFQCTJZDRC-UHFFFAOYSA-N 1,2-hexadecanediol Chemical compound CCCCCCCCCCCCCCC(O)CO BTOOAFQCTJZDRC-UHFFFAOYSA-N 0.000 description 1
- VPVXHAANQNHFSF-UHFFFAOYSA-N 1,4-dioxan-2-one Chemical compound O=C1COCCO1 VPVXHAANQNHFSF-UHFFFAOYSA-N 0.000 description 1
- AOLNDUQWRUPYGE-UHFFFAOYSA-N 1,4-dioxepan-5-one Chemical compound O=C1CCOCCO1 AOLNDUQWRUPYGE-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- WKRCUUPMCASSBN-UHFFFAOYSA-N 2,2-diethylbutanedioic acid Chemical compound CCC(CC)(C(O)=O)CC(O)=O WKRCUUPMCASSBN-UHFFFAOYSA-N 0.000 description 1
- OWBTYPJTUOEWEK-UHFFFAOYSA-N 2,3-Butanediol Chemical group CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 1
- LXVSANCQXSSLPA-UHFFFAOYSA-N 2-Ethyl-2-Hydroxybutyric acid Chemical compound CCC(O)(CC)C(O)=O LXVSANCQXSSLPA-UHFFFAOYSA-N 0.000 description 1
- AFENDNXGAFYKQO-UHFFFAOYSA-N 2-Hydroxybutyric acid Chemical compound CCC(O)C(O)=O AFENDNXGAFYKQO-UHFFFAOYSA-N 0.000 description 1
- FDYJJKHDNNVUDR-UHFFFAOYSA-N 2-ethyl-2-methylbutanedioic acid Chemical compound CCC(C)(C(O)=O)CC(O)=O FDYJJKHDNNVUDR-UHFFFAOYSA-N 0.000 description 1
- NGEWQZIDQIYUNV-UHFFFAOYSA-N 2-hydroxy-3-methylbutyric acid Chemical compound CC(C)C(O)C(O)=O NGEWQZIDQIYUNV-UHFFFAOYSA-N 0.000 description 1
- GHPVDCPCKSNJDR-UHFFFAOYSA-N 2-hydroxydecanoic acid Chemical compound CCCCCCCCC(O)C(O)=O GHPVDCPCKSNJDR-UHFFFAOYSA-N 0.000 description 1
- RGMMREBHCYXQMA-UHFFFAOYSA-N 2-hydroxyheptanoic acid Chemical compound CCCCCC(O)C(O)=O RGMMREBHCYXQMA-UHFFFAOYSA-N 0.000 description 1
- NYHNVHGFPZAZGA-UHFFFAOYSA-N 2-hydroxyhexanoic acid Chemical compound CCCCC(O)C(O)=O NYHNVHGFPZAZGA-UHFFFAOYSA-N 0.000 description 1
- BWLBGMIXKSTLSX-UHFFFAOYSA-N 2-hydroxyisobutyric acid Chemical compound CC(C)(O)C(O)=O BWLBGMIXKSTLSX-UHFFFAOYSA-N 0.000 description 1
- JYZJYKOZGGEXSX-UHFFFAOYSA-N 2-hydroxymyristic acid Chemical compound CCCCCCCCCCCCC(O)C(O)=O JYZJYKOZGGEXSX-UHFFFAOYSA-N 0.000 description 1
- JKRDADVRIYVCCY-UHFFFAOYSA-N 2-hydroxyoctanoic acid Chemical compound CCCCCCC(O)C(O)=O JKRDADVRIYVCCY-UHFFFAOYSA-N 0.000 description 1
- JRHWHSJDIILJAT-UHFFFAOYSA-N 2-hydroxypentanoic acid Chemical compound CCCC(O)C(O)=O JRHWHSJDIILJAT-UHFFFAOYSA-N 0.000 description 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N 3-aminopropanol Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
- CVLOFBQBRWAGKC-UHFFFAOYSA-N 3-hexyloxan-2-one Chemical class CCCCCCC1CCCOC1=O CVLOFBQBRWAGKC-UHFFFAOYSA-N 0.000 description 1
- SXFJDZNJHVPHPH-UHFFFAOYSA-N 3-methylpentane-1,5-diol Chemical compound OCCC(C)CCO SXFJDZNJHVPHPH-UHFFFAOYSA-N 0.000 description 1
- IGIDLTISMCAULB-UHFFFAOYSA-N 3-methylpentanoic acid Chemical compound CCC(C)CC(O)=O IGIDLTISMCAULB-UHFFFAOYSA-N 0.000 description 1
- OSKVFHONCZMKCM-UHFFFAOYSA-N 4,6,6-trimethyloxepan-2-one Chemical compound CC1CC(=O)OCC(C)(C)C1 OSKVFHONCZMKCM-UHFFFAOYSA-N 0.000 description 1
- HEXADYGOPKQMSD-UHFFFAOYSA-N 5-(hydroxymethyl)oxepan-2-one Chemical compound OCC1CCOC(=O)CC1 HEXADYGOPKQMSD-UHFFFAOYSA-N 0.000 description 1
- FBGOPBALJSIXQZ-UHFFFAOYSA-N 5-nonyloxepan-2-one Chemical compound CCCCCCCCCC1CCOC(=O)CC1 FBGOPBALJSIXQZ-UHFFFAOYSA-N 0.000 description 1
- GZGQVPASOBQUKB-UHFFFAOYSA-N 6-methyloxepan-2-one Chemical compound CC1CCCC(=O)OC1 GZGQVPASOBQUKB-UHFFFAOYSA-N 0.000 description 1
- PZZYQPZGQPZBDN-UHFFFAOYSA-N Aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N Aminocaproic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- RDOXTESZEPMUJZ-UHFFFAOYSA-N Anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 238000006220 Baeyer-Villiger oxidation reaction Methods 0.000 description 1
- 239000002028 Biomass Substances 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N Bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- CLZBQDSEAVOBJU-UHFFFAOYSA-N C(CCC(=O)OC)(=O)OCC.C(CCCCC)(O)O Chemical compound C(CCC(=O)OC)(=O)OCC.C(CCCCC)(O)O CLZBQDSEAVOBJU-UHFFFAOYSA-N 0.000 description 1
- 229960003563 Calcium Carbonate Drugs 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- FLKPEMZONWLCSK-UHFFFAOYSA-N Diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 1
- UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 1
- ORAWFNKFUWGRJG-UHFFFAOYSA-N Docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)=O ORAWFNKFUWGRJG-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 101700000128 HACL1 Proteins 0.000 description 1
- 102100001922 HACL1 Human genes 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N Isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- LOCYSVHOSYQGOV-UHFFFAOYSA-N N-hexyl-6-$l^{1}-azanyl-6-oxohexanamide Chemical compound [CH]CCCCCNC(=O)CCCCC([N])=O LOCYSVHOSYQGOV-UHFFFAOYSA-N 0.000 description 1
- VMRGZRVLZQSNHC-UHFFFAOYSA-N N-octadec-9-enylhexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)NCCCCCCCCC=CCCCCCCCC VMRGZRVLZQSNHC-UHFFFAOYSA-N 0.000 description 1
- 210000003739 Neck Anatomy 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 101710036925 Os01g0505400 Proteins 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N Phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 229960000380 Propiolactone Drugs 0.000 description 1
- 229940037312 STEARAMIDE Drugs 0.000 description 1
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001280 alpha hydroxy acids Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000006085 branching agent Substances 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbamate Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003426 co-catalyst Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001143 conditioned Effects 0.000 description 1
- 150000005676 cyclic carbonates Chemical class 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- INSRQEMEVAMETL-UHFFFAOYSA-N decane-1,1-diol Chemical compound CCCCCCCCCC(O)O INSRQEMEVAMETL-UHFFFAOYSA-N 0.000 description 1
- YSRSBDQINUMTIF-UHFFFAOYSA-N decane-1,2-diol Chemical compound CCCCCCCCC(O)CO YSRSBDQINUMTIF-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing Effects 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- JJTUDXZGHPGLLC-UHFFFAOYSA-N dilactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GHLKSLMMWAKNBM-UHFFFAOYSA-N dodecane-1,12-diol Chemical compound OCCCCCCCCCCCCO GHLKSLMMWAKNBM-UHFFFAOYSA-N 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
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- 125000000524 functional group Chemical group 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
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- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium(0) Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
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- 239000008079 hexane Substances 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229920004889 linear high-density polyethylene Polymers 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
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- 238000011068 load Methods 0.000 description 1
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- 239000004702 low-density polyethylene Substances 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
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- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
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- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
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- QZCLKYGREBVARF-UHFFFAOYSA-N tributyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
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- TUWSWCCZNGVWQR-UHFFFAOYSA-N trihexyl 2-hydroxy-4-oxopentane-1,2,3-tricarboxylate Chemical compound CCCCCCOC(=O)CC(O)(C(=O)OCCCCCC)C(C(C)=O)C(=O)OCCCCCC TUWSWCCZNGVWQR-UHFFFAOYSA-N 0.000 description 1
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Abstract
Lactone copolymers are disclosed which are polymerized from a first lactone monomer and a second amorphous monomer which is effective to suppress the crystallization of the copolymer. It is disclosed that suppression of the crystallization can provide enhanced mechanical properties in films made from the copolymers. As a result, films prepared from the copolymers of the present invention can have properties rendering them suitable for use as biodegradable trash bags as well as for other uses.
Description
LACTONE COPKLYMERS. BIODEGRADABLES
FIELD OF INVENTION The present invention relates to condensation copolymers, polyesters, having crystallinity removed which can make them suitable for use, for example, in the manufacture of biodegradable films for garbage bags.
BACKGROUND OF THE INVENTION Current environmental aspects have generated interest in the use of biodegradable plastics for disposable articles such as, for example, garbage bags, packaging materials, food utensils and the like. A series of biodegradable polymers have been proposed for such uses, usually these polymers include condensation polymers such as, for example, polyesters, polyester amides, polymers formed by ring-opening polymerization, for example, lactone polymerizations, reading and lactam, polyhydroxyalkonatides, polylactic acid and natural polymers such as polysaccharides, for example, cellulose, starch and soy derivatives. As used herein, the term "biodegradable", as defined in ASTM D-883, is made with reference to degradable polymers in which degradation results from the action of natural microorganisms such as, for example, bacteria, fungi and algae. Biodegradability can be checked, for example, by the production of CO2 and the associated reduction in mechanical properties such as tensile strength and percent elongation at break. Other details are known to those skilled in the art. Although many polymers such as those described above are highly effective in terms of their biodegradability, they often exhibit inferior mechanical performance that has impeded their commercial viability. More specifically, when they are converted into film by extrusion of blown film, for example, biodegradable polymers usually do not have good machine direction ("MD") tear resistance The endorph measured by ASTM D-1922, transverse direction (" TD ") Tensile strength as measured by ASTM D-1822, impact strength of a falling dart measured by ASTM D-1709, secant modulus MD and TD measured by ASTM D-882, and puncture resistance measured by the test of Union Carbide method C-68-L. On the other hand, when biodegradable polymers are modified to improve their mechanical properties, their biodegradability is often affected. As used herein, the terms "condensation polymerization" and "polycondensation" mean: (i) a polymerization reaction in which two or more molecules combine with the generation of water, alcohol or other simple substances as by-products; and (ii) the polymerization of the monomers, for example, ester and amide monomers, formed by ring-opening polymerization, for example, lactones, lactides and lactams that do not generate water, alcohol or other simple substances as by-products.
Frequently condensation polymers suitable for use as biodegradable materials are semi-crystalline in form, for example, more than about 30% by weight, often greater than about 50% by weight and more frequently greater than about 70% by weight crystalline. The complete crystallization of polymers is often a slow process that takes minutes, hours or days to complete. When crystallization is desired, the temperature is maintained above the glass transition temperature ("Tg") and below the crystalline melting point for a sufficient time to allow the polymer molecules to be arranged in crystal lattices. This process is also known in the art as "annealing." If the crystallinity of the polymer becomes too high, the molded polymer article may not have sufficient rigidity to be possible in a common end use such as garbage bags, tarred film, molded parts and the like.
Accordingly, condensation polymers are desired, for example, lactone polymers, having improved mechanical properties and retaining their biodegradable characteristics.
SUMMARY OF THE INVENTION The improved lactone polymers are obtained by the present invention. The improvement of the present invention is directed to the use of the comonomers in the condensation polymerization which are effective to eliminate the crystallinity of the copolymers. Without adhering to any specific theory, it is considered that the removal of the crystallinity can make improvements in the mechanical properties of the films prepared from the copolymers compared to the copolymers prepared without the crystallinity-eliminating monomers. According to the present invention, the elimination of the crystallinity can be evidenced by one more factors. For example, the removal of the crystallinity may be evident by a reduction in the crystallization temperature of the copolymer, or by a reduction in the crystallization rate of the copolymer, or by a reduction in the melting temperature of the polymer or by a reduction in the crystallinity of the copolymer. As used herein, the term "crystallization temperature" means the temperature at which the formation of the crystalline phase occurs; the term "crystallization rate" means the rate at which the formation of the crystalline phase occurs; the term "melt temperature" means the freezing point and the term "crystallinity" means the degree of crystallinity of the polymer. The crystallization properties of the polymers can be readily determined by those skilled in the art, such as for example by differential scanning calorimetry ("DSC").
DETAILED DESCRIPTION OF INVENTION The first suitable monomer for use according to the present invention is a lactone monomer. The first monomer may be ethylenically unsaturated or otherwise may not have ethylenic unsaturation. The molecular structure of the first monomer is not crucial for the present invention and can be straight, for example, normal, alkyl or branched, cyclic or aromatic substituents. In addition, the first monomer can be composed of a single molecular unit, an oligomer or a prepolymer and can have a molecular weight of, typically, from about 72 to 12,000 grams per gram mol ("g / gmol"), more commonly , from about 72 to 10,000 g / gmol. Unless stated otherwise, as used herein, the term "molecular weight" means the numerical average molecular weight. Techniques for determining numerical average molecular weight are known to those skilled in the art. One of these techniques is gel permeation chromatography ("GPC"). In one aspect of the present invention, the cyclic monomers include those having the formulas:
where X = nil, -0-, or -0-C = 0; Z = 1-3; Y = 1-4; R1-R4 = H-, - CH3, C2-C? 6 alkyl group of C2-C16-C (CH3), or HOCH2-, and where all R are independent in each carbon unit and or z independent of each other; or
where R1-R4 = H-, -CH3, C2-C16 alkyl group, or H0CH2-, and where all R are independent from each other. Examples of the lactones described above are, but are not limited to, e-caprolactone, t-butyl caprolactone, z-enantolactone, deltavalerolactones, monoalkyl-delta-valerolactones, for example, monomethyl-, monoethyl-, monohexyl-deltavalerolactones. and the like; nonalkyl, dialkyl and trialkyl-epsilon-caprolactones, for example, monomethyl-, monothii-, monohexyl-, dimethyl-, di-n-propyl-, di-n-hexyl-, trimethyl-, triethyl-, tri-n- epsilon-caprolactones, 5-nonyl-oxepan-2-one, 4,4,6- or 4,6,6-trimethyl-oxepan-2-one, 5-hydroxymethyl-oxepan-2-one, similar; beta-lactones, for example, beta-propiolactone, beta-butyrolactone, gamma-lactones, for example, gamma-butyrolactone or di-alolactone, dilactones, for example, lactide, dilactides, glycolides, for example, tetramethyl glycolides and the like, ketodioxanones, for example , 1,4-dioxan-2-one, 1,5-dioxepan-2-one, and the like. The lactones may consist of the optically pure isomers or two or more optically different isomers or may consist of mixtures of isomers. The e-caprolactone and its derivatives and other 7-membered lactones in the ring are especially preferred for use as the first monomers according to the present invention. In an aspect of the present invention, other monomers can be polymerized with the lactones to comprise the first monomer, such as, for example, one or more compounds that can be polymerized or copolymerized to form aliphatic polyesters or polyester amides or other condensation polymers. Examples of these polymers include, for example, polyesters prepared from the reaction of C2-C6 diols, for example ethylene glycol, diethylene glycol, butanediol, neopentyl glycol, hexanediol, with dicarboxylic acids such as, but not limited to, , succinic, glutaric or adipic acid; polymer copolymers of terephthalic acid base with dicarboxylic acids and diols; and polyester / amides from the reaction of caprolactam with dicarboxylic acids and diols. Suitable hydroxy acids include, for example, α-hydroxybutyric acid, α-hydroxyisobutyric acid, α-hydroxyvaleric acid, α-hydroxyisovaleric acid, α-hydroxycaproic acid, α-hydroxyisocaphoic acid, α-hydroxy-α-ethylbutyric acid, α-hydroxy acid. ß-methylvaleric acid, α-hydroxyheptanoic acid, α-hydroxyoctanoic acid, α-hydroxydecanoic acid, α-hydroxymyristic acid and α-hydroxysteic acid or their intermolecular cyclic esters or combinations thereof. In another aspect of the present invention the first monomer may further comprise cyclic monomers which are polymerized by polymerization with. ring opening in addition to the lactones. Common to these monomers are cyclic esters such as, for example, lactides, glycolides and cyclic carbonates. Examples of the common cyclic ester polymers and their (co) olomers resulting from the polymerization of the aforementioned monomers include: poly (epsilon-caprolactone); poly (L-lactide-co-epsilon-caprolactone); poly (D, L-lactide-co-epsilon-caprolactone); poly (meso-lactide-co-epsilon-caprolactone); poly (glycolide-co-epsilon-caprolactone). Usually, the amount of the first monomer used in the copolymers of the present invention is from about 50 to 99% by weight, preferably from about 60 to 98% by weight and more preferably from about 85 to 95% by weight, based on the total weight of the monomers in the copolymer. Monomers suitable for use as the first monomer in the copolymers of the present invention are available commercially. The second monomer suitable for use in the preparation of the copolymers of the present invention includes any of the amorphous monomers that are functional to remove the crystallinity of the copolymer. As used in the present invention, the term "amorphous" means that the monomer is primarily amorphous, ie, more than 50% amorphous, preferably greater than 70% amorphous and more preferably greater than 90% amorphous, determined, by example, DSC measuring the enthalpy of fusion. The second monomer may be ethylenically unsaturated or otherwise may not have ethylenic unsaturation. The molecular structure of the second monomer is not crucial for the present invention and can be straight, for example, normal, alkyl or branched, cyclic or aromatic. In a preferred aspect of the invention, the second monomer is a branched ester. Preferably, the second monomer has a functional group selected from 1Q
group consisting of esters, ethers, alcohols, acids, amides, acid halides and mixtures thereof. In addition, the second monomer can be composed of a single molecular unit, an oligomer or a prepolymer and can have a molecular weight usually from about 62 to 12,000 g / gmol, more commonly from about 62 to 10,000 g / gmol. Moreover, the second monomer may comprise a derivative of the first monomer, for example, a branched caprolactone such as, for example, t-butyl lactone. In the polymerization of the first monomer, the second monomer is usually used as an initiator, for example to initiate the ring opening of the cyclic lactone monomers. Usually, the removal in the crystallinity produced by the second monomer will be evidenced by one or more of the following factors: (i) a reduction in the crystallization temperature of the copolymer of at least 2 ° C, preferably at least 4 ° C. C and more preferably at least ß ° C, compared to a homopolymer of the first monomer or a copolymer of the first monomer and another monomer that is not effective in removing the crystallinity, or (ii) a reduction in the crystallinity of the copolymer. Usually, according to the present invention, the crystallinity will be reduced by at least 2%, preferably by at least 6% and most preferably by at least 8% compared to the crystallinity of a homopolymer of the first monomer or a copolymer of the first monomer and another monomer that is not effective in suppressing crystallinity. The crystallinity can be determined by DSC, measuring the enthalpy of fusion. In one aspect of the present invention, the second monomer is effective to create amorphous regions in the copolymer. For example, if the second monomer is a branched version of the first monomer, it will generally not co-crystallize with the first monomer, it will thus break the crystallization of the first monomer by increasing the amorphous region, decreasing the crystallinity of the copolymer. If the second "monomer" is a non-crystallizable oligomer, the net crystallinity of the copolymer will be reduced to a level that can improve the stiffness of the molded polymer. In one aspect of the present invention, the second monomer is effective to introduce branching into the polymer, i.e., chains pendant from the main chain of the copolymer. Preferably, the branching is introduced with short chains in the main structure of the copolymer. As used herein, the term "short chain branching" means hydrocarbon branching, for example, alkyl groups in the polymer backbone, which are preferably C __-Ci6 alkyl groups, ending in a free end. unreacted, for example, methyl, propyl, t-butyl. Branching with short chains can be introduced into the polymer backbone, for example, using branched difunctional initiators obtained by polymerizing a linear or branched dicarboxylic acid with a linear or branched diol initiator, so that at least the acid or diol is branched . Suitable dicarboxylic acids are of the formula:
where Y = 0 to 12; Ri and R2 = H-, -CH3 or alkyl group of C-C ?, and where all R are independent of each other and each carbon unit. Examples of the dicarboxylic acids are succinic acid, glutaric acid, adipic acid, suberic acid, sebacic acid, dodecandioic acid and 2-ethyl-2-ethylsuccinic acid. In addition to the aliphatic dicarboxylic acids described above, it is also possible to use the aromatic dicarboxylic acids such as, but not limited to, phthalic acid, isophthalic acid, and terephthalic acid. Suitable diol initiators are of the formula:
where X = nil, -0-; a = 1 to 6; b = a to 1Q; c = ni, C? -C? g [sic]; and Ri-R4 = H-, -CH3, or C2-C_6 alkyl group, and where all R are independent of each other and of each carbon unit. The examples of the diols are, but are not limited to, ethylene glycol, diethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,6-hexanediol, 1,1-decanediol, 1,12-dodecanediol, 1,2-decanediol, , 2-dodecanediol, 1,2-hexadecanediol, neopentyl glycol, 3-methyl-1, 5-pentanediol, 2-methyl-1-3-propanedial, -2-butyl-2-ethyl-1,3-propanediol, 2- ethyl-3-butyl-l, 3-propanediol, 2-ethyl-l, b-hexanediol. Of these, the adipate of 2-butyl-2-ethyl-1,3-propane, prepared from the reaction of 2-butyl-2-ethyl-1,3-propanediol ("BEPD") and adipic acid, is preferred. Other methods of introducing short chain branching include the reaction of branched or long chain 1,2-diol with the monomer e-caprolactone and then transesterification with the diester of dicarboxylic acid, for example, the transesterifation of an initiated caprolactone oligomer with BEPD with dimethyl adipate, or the reaction of an oligomer caprolactone initiated with BEPD with adipoyl chloride, or the reaction of a caprolactone oligomer initiated by BEPD with a diisocyanate, i.e. HDl or MDl, or by reacting branched lactones with non-lactones branched, for example, the copolymer of t-butylcaprolactone and e-caprolactone. As an alternative or in addition to the branched, polymerized monomers, the branched polymers may be combined in linear polymers of other molecules to provide branching of short chains. The amount of the second monomer suitable for use in the preparation of the copolymers of the present invention is effective in removing the crystallinity of the copolymer. The amount is usually from about 1 to 50% by weight, preferably from about 5 to 35% by weight and more preferably from about 9 to 20% by weight, based on the total weight of the monomers used to prepare the copolymer. The optimum level of the second monomer will depend on the specific structure of the second monomer can be determined by those skilled in the art. In the preparation of the copolymers of the present invention it is possible to use one or more monomers of the first group of monomers or of the second group of monomers. In addition, it is also possible to use other monomers in addition to the first monomer and the second monomer. Such other monomers can be introduced, for example, to impart certain desired properties to the copolymer. The other particular monomers are not crucial to the present invention but may include, for example, monomers such as alcohols, for example, ethylene glycol, 1-butanediol, 1,3-propanediol, 1,6-hexanediol, diethylene glycol, etc. dicarboxylic acids, for i?
example, oxalic acid, succinic acid, adipic acid, amino alcohols, for example, ethanolamine, propanolamine, amino carboxylic acids, for example, aminocaproic acid, and the like. In addition, it is possible to use other monomers that are normally used to prepare traditional non-biodegradable polymers such as polyethylene (including low density polyethylene, linear low density polyethylene and high density polyethylene), ethylene-acetate copolymers of vinyl, ethylene-acrylic acid copolymers, polyvinyl chloride, polystyrenes. chlorinated polyethylenes, ethylene propylene copolymers, acrylic acid copolymers, polyvinylacetal copolymers, polyanes, polyethylene terephthalates, phenolic resins and urethanes. In addition to other monomers, the copolymers of the present invention may be combined and / or reacted with other polymers to provide the desired characteristics. For example, the copolymers of the present invention can be extruded with other polymers such as, for example, polysaccharides, for example starch, cellulosics, quitanas and the like. More details of these mixed polymer compositions are known to those skilled in the art. See, for example, U.S. Patent No. 5,095,054 which is directed to thermoplastic polymer compositions comprising destructurized starch and other polymers, U.S. Patent No. 5,540,929 which is directed to aliphatic polyester grafted polysaccharides. Usually, the amount of these other monomers, when used in the copolymers of the present invention, is from about 1 to 90% by weight. Usually, when the copolymers of the present invention are mixed or reacted with other polymers the amount of the other polymer is usually from about 0 to 70% by weight, and preferably from about 20 to 60% by weight and greater preferably from about 30 to 40% by weight, based on the total weight of the mixed polymer composition.
Another aspect of the present invention is directed to the introduction of branching of long chains in the polymer backbone. In this aspect of the invention, the long chain branching can be incorporated into the polymer backbone or the long chain branching polymers can be combined with the copolymers to improve processability. As used herein, the term "long chain branching" means hydrocarbon branches, for example, alkyl groups in the main chain terminating in more than two reactive end groups that give rise to the preparation of non-linear polymers. Examples of the long chain branching polymers are, but are not limited to, e-caprolactone polymers with multifunctional initiators such as trimethylol propane, pentaerythritol, dipentaerythritol and other molecules with multiple hydroxyl groups or other reactive groups. The improved processing capacity of the copolymers of the present invention can be measured, for example, by determining their index values of the Relaxation Spectrum (RSI). As used herein, the terms "Relaxation Spectrum Index" and "RSI" mean the amplitude of the distribution of molecular relaxations in the molten state calculated from dynamic oscillatory shear tests run in a frequency range from 0.1 to 100 1 / sec. The RSI is a sensitive indicator of the molecular structure, such as the branching of long chains, which causes a long relaxation time behavior in the molten state. Other details related to the RSI are known to those skilled in the art. See, for example, J. M. Dealy and K. F. Wissbrun, Met Rheology and Its Role in Plastics Processing, Van Nostrand Reinhold, 1990, p. 269-297 and S. H. asserman, J. Rheology, vol. 39, pp. 601-625 (1995). The processes used to prepare the copolymers of the present invention are not crucial. The polymer of the present invention can be prepared by bulk polymerization, suspension polymerization, extruder polymerization or solution. The polymerization can be carried out, for example, in the presence of an inert organic carrier.
normally liquid as may be, for example, aromatic hydrocarbons, for example, benzene, toluene, xylene, ethylbenzene and the like; oxygenated organic compounds such as anisole, dimethyl and ethylene glycol diethyl esters; normally liquid hydrocarbons including saturated, cyclic, and cyclic alkyl-substituted saturated hydrocarbons such as hexane, heptane, cyclohexane, decahydronaphthelene, and the like. The polymerization process can be carried out in a batch, semi-quantum or continuous form. The monomers and catalysts can be mixed in any order according to the known polymerization techniques. Thus, the catalyst can be added to a comonomeric reagent. Then, the comonomer containing the catalyst can be mixed with another comonomer. In the alternative, the comonomeric reagents can be mixed together. The catalyst can then be added to the reaction mixture. If desired, the catalyst can be dissolved or suspended in a normally liquid, inert organic carrier. If desired, the monomer reagents as a solution or suspension in an inert organic vehicle can be added to the catalyst, catalyst solution or catalyst suspension. Still further, the catalyst and the comonomeric reagents can be added at the same time to a reaction vessel. The reaction vessel may be equipped with a traditional heat exchanger and / or mixing device. The reaction vessel can be any equipment normally used in the polymer manufacturing art. A suitable container, for example, is a stainless steel container. If used, a plasticizer or a solvent may be mixed in the polymer to help separate the polymeric material from the reaction vessel. Typically, the polymerization reactions are carried out at a temperature of from about 70 to 250 ° C, preferably from about 100 to 220 ° C, during a reaction time from about 3 minutes to 24 hours, preferably from about 5 to 10 hours. The reaction pressure is not crucial for the present invention. The specific catalyst used in the polymerization is not crucial and can be determined by those skilled in the art. However, a preferred catalyst for the polymerization of caprolactone with adipate BEPD is tin carboxylate. The catalyst and the initiator can be combined in the same molecules, for example, an aluminum alkoxide. In addition to the monomers it is possible to add other ingredients, such as plasticizers, for example, epoxidized soy bean oil, epoxidized linseed oil, triethyl citrate, acetitriethyl citrate, 7Q citrate.
tri-n-butyl, acetyltri-n-butyl citrate, acetyltri-n-hexyl citrate, glycerin, diethyl phthalate, dioctyl phthalate, antiblocks, for example, stearamide, behenamide, oleoamide, erucamide, stearilerucamide, erusilerucamide, oleylpalmitamide, stearyltearamide, erusyl-stellate N, N'-ethylenebistearamide, N, N'-ethylenebisoleamide, talc, calcium carbonate, kaolin clays, molecular sieves and other particulate materials, stabilizers, co-catalysts, nucleating agents, pigments, etc. Typically, the total amount of these other ingredients is in the range of from about 0.01 to 10% by weight, based on the total weight of the copolymer composition. More details related to the selection and quantity of these additives are known to those skilled in the art. The copolymers produced according to the present invention usually have a melting point from about 50 to 240 ° C, preferably from about 52 to 120 ° C, and a Tg from about -120 to 120 ° C and preferably from about -60 to 60 ° C. Copolymers typically have a melt flow of from about 0.1 to 7, preferably from about 0.2 to 2.5 and more preferably from 0.5 to 2. As used herein, the term "Melt Flow" means grams. of material flowing through a nozzle in 10 minutes at 125 ° C / 2.16 kilograms ("kg") as described in ASTM D-1238.
The density of the copolymers is usually in the range from about 1.00 to 1.50 grams per cubic centimeter ("g / cc") and preferably from about 1.0 to 1.20 g / cc. Preferably, the addition of amorphous blocks or branching (short and / or long chain) will reduce the density of the copolymer relative to the homopolymer in the solid state. The reduction in density can give rise to better polymer stiffness properties. Preferably, the copolymers of the present invention have a reduction in density of at least Q.QQ4 g / cc and more preferably from about 0.004 to 0.040 g / cc relative to the homopolymer of the first monomer (exclusive of the initiator.) Typically, the copolymers of the present invention have a weight average molecular weight (Mw) of from about 500 to 800,000 grams / gram mol, and preferably from about 50,000 to 500,000 grams / gram mol. Usually the number average molecular weight (Mn) is in the range from about 500 to 700.00 grams / gram mole, preferably from about 30,000 to 500,000 grams / gram mole. The polydispersity index (Mw / Mn) is usually in the range from about 1.3 to 10. Upon completion of the polymerization reaction, the copolymers can be recovered by any means known to those skilled in the art. Preferably, according to the invention, the copolymer is transported in its molten state directly to a granulator, extruder or molding machine to produce the desired product. These products can be produced in any manner known to those skilled in the art, such as for example fibers, granules, molded articles, films, sheets and the like. The films containing the copolymer compositions of the present invention can be converted into cast or blown films, sheets, blow molded, injection molded or fiber spun using any process or equipment known to those skilled in the art. Normally the films have a thickness from about 0.5 to 2 mils preferably from about 0.6 to 1.7 mils, and more preferably from about 0.7 to 1.5 mils. The mechanical properties mentioned herein are based on a film thickness of 1.0 to 1.3 mils. Typically, the films have an MD tensile strength from about 3000 to 9000 psi, preferably from about 4000 to 8000 psi, with an elongation at MD break of about 250 to 900%, preferably from about 400 to 800%, measured by A.STM D-882. Typically, the films have a tensile strength TD from about 2000 to 8000 psi, preferably from about 4000 to 6000 psi, with an elongation at break from about 300 to 1000%, preferably from about 500 to 900%. The shock properties of falling a dart in films is usually in the range from about 20 to 200 grams per 1/1000 inches ("g / mil"), preferably at least 50 g / mil and greater preference in the range from about 50 to 150 g / thousand. The elmendorf MD tearing properties of the films is usually in the range from about 5 to 200 g / mil and preferably in the range from about 15 to 150 g / mil. The tearing properties elmendorf TD of the films usually is in the range from 1QQ to 70Q g / thousand and preferably in the range from about 100 to 700 g / mil. The MD secant modulus properties of the films are usually in the range from 60,000 to 100,000 psi and preferably in the range from about 30,000 to 80,000 psi. The TD blot module properties of the films are usually in the range of 70,000 to 130,000 psi and preferably in the range of about 30,000 to 80,000 psi. The MD tensile shock properties of films are usually in the range of 400 to 1100 ft.-lbs./in.in. and preferably in the range of about 400 to 1700 ft.-lb./sc. The TD tensile shock properties of films are usually in the range of 70 to 1100 ft-lb / cu in and preferably in the range of about 200 to 1700 ft-lb / cu [sic]. The puncture resistance properties of films are usually in the range of 3 to 50 in-lbs / mil and preferably in the range of about 10 to 50 in-lbs / mil. The copolymers of the present invention can be used in the manufacture of a wide range of products that includes, for example, sheets, ie, greater than 10 mil thick, films, that is, less than 10 mil thick, for example, garbage bags, fibers, for example, sutures, fishing lines and non-woven fabrics and molded articles, for example, containers, tools and medical devices co or can be, for example, staples, clips, pins, prostheses, etc. A particularly preferred end-use according to the present invention is to provide compostable films for use as a garbage bag. As defined in ASTM D-883, a compostable plastic is a plastic that undergoes biological degradation during compost deformation to produce carbon dioxide, water, inorganic compounds and biomass at a rate consistent with other known compostable materials and leaves no residue visually distinguishable or toxic. In general, the copolymers of the present invention are practically biodegradable. More specifically, the copolymer compositions are generally biodegradable and can be composted by ASTM D-5338, which is a standard test method for Determination of Aerobic Biodegradation of Plastic Materials under controlled conditions for the formation of compost.
Examples The following examples are provided for illustrative purposes and are not intended to limit the scope of the following claims. The following test procedures were used in the examples.
GPC procedure The GPC was performed on an HPCL Waters 590 unit with an LC-241 autosampler, Waters Styragel HR-1, HR-3, HR-4, HR-4E, HR-5E, a ERMA ERC differential refractometer detector -7510 connected to a VG data system, using tetrahydrofuran (stabilized with BHT), as the solvent, disposable 0.45u PTFE filters (for sample preparation) and a nylon 66 filter of 0.45u (to degas the mobile phase). The unit was calibrated using polystyrene standards in the molecular weight range of 162 to 1,800,000. The operating parameters were: Flow 1.0 ml / in Run time 65 minutes Injection size 200 ul Temperatures 35c [sic] Ambient columns Ambient injector
The concentration of the sample was 0.5% by weight / volume.
Melt flow The melt flow of the polymers was determined using ASTM D-1238. The determinations were made at a temperature of 125 ° C and a pressure of 2.16 kg.
Density The density of the polymers was determined using ASTM D-1505, Density per Gradient Column.
Film properties Except for the perforation resistance, film properties were measured using the appropriate ASTM test procedure, eg, ASTM D-1709 for impact resistance by the falling dart
(Also known herein as "dart drop.) The puncture resistance of the film was measured using the Union Carbide Corporations WC-68-L method, and is a test procedure known to those skilled in the art ( also known herein as "puncture resistance".) Puncture resistance is defined as the force required to break a test sample and the energy absorbed by the film during the break. , which measures the high-speed impact, the resistance, the perforation uses a piston in slow motion moving at a crosshead speed of 20 inches / minute, an Instron Traction Tester, CVC compression cell (model G-Q3- 2), integrator, film and piston carrier, weights for calibration and micrometer Five samples of 6 by 6 inches of each film are prepared and conditioned for 40 hours at 23 ± 2 ° C and relative humidity of 50 ± 5%. The thickness of each film is measured in the center to the nearest 0.0001 inch and mounted on the compression cell so that the piston will puncture the center of the film. The piston is placed 8 inches above the compression cell and will have a downward stroke of 6 inches. The load in pounds needed to break the samples is recorded and the results reported as in-lbs / il. Differential Scanning Calorimetry (DSC) The DSC for polymers was measured in a helium sphere from -100 ° C to '^ ° at a speed of 10 ° C / minute. Instead of the properties of 1 film, the effect of crystalline removal by the addition of an amorphous block or short chain branching was determined using DSC. The effect is shown with a depression of the crystallization temperature (Te), and in a second heat depression of the melting point (Tm2) and a decrease in the crystallinity as measured by a reduction in the heat of fusion (? Hf) .
Index of the relaxation spectrum The RSI of the polymer is determined by first subjecting the polymer to a shear deformation and measuring its response to deformation using a rheometer. As is known in the art, based on the response of the polymer and the mechanics and geometry of the rheometer used, the relaxation module G (t) or the dynamic modules G '(VJ) and G "(VJ) were determined as functions of time or frequency.
Biodegradability ASTM D-5338, which is a standard test method for the Determination of Aerobic Biodegradation of Materials
Plastics under Controlled Conditions for the Training of
Compost, was used to determine the biodegradability of the copolymer. In the examples the following ingredients were used.
TONE® Monomer ECEQ - an e-caprolactone monomer available from
Union Carbibe Corporation, Danbury, CT. TONE Polymer P-787 an 80,000 Mn polymer available from
Union Carbibe Corporation, Danbury, CT. TONE Polymer P-767 a polymer of 43,000 Mn available from
Union Carbibe Corporation, Danbury, CT. TONE Polymer P-300 a polymer of 10,000 Mn available from
Union Carbibe Corporation, Danbury, CT.
EXAMPLE 1 PREPARATION OF BRANCHED BEPD ADIPATE MONOMERS BEPD adipates in the molecular weight range from 4000 to 21000, determined by GPC, were prepared in a 4-neck resin kettle equipped with a condenser and a Dean Stark trap, stirrer, Nitrogen sprayer tube and flow meter, and a thermocouple connected to a mantle or heating jacket with controlled temperature. On a molar basis, the reactor was charged with the appropriate amount of BEPD, adipic acid and toluene at 10% by weight as an azeotrope solvent. The azeotrope solvent is included to separate the produced water as a byproduct of the reaction. The reaction was carried out under nitrogen and heated to 140 ° C. After stopping collecting the water in the Dean Stark trap, the temperature was raised in increments of 20 ° C to 220 ° C and held until it was obtained > 95% of the theoretical amount of water that was to be separated. The temperature was reduced to 160 ° C, an adequate amount of a metal carboxylate catalyst was charged, the temperature was raised to a maximum of 220 ° C and the reaction was allowed to continue for 12 to 16 hours. The acidity index was determined and if it was > 4 additional catalyst was added and the reaction was continued until the acid number was > 4. The acidity index and the molecular weight per GPC of the product were determined.
EXAMPLE 2 PREPARATION OF ADIPATQ CQPQLÍMERQS OF RAMIFIED BEPD
CAPRQLACTQNA Caprolactone copolymers / BEPD adipates with molecular weights GPC > 40, 000, in a pot of resin with four necks, equipped with a stirrer, nitrogen spray tube and flow meter, a thermocouple connected to an oil bath with controlled temperature and vacuum. On a molar basis, the reactor was charged with a suitable amount of the monomer e-caprolactone and the adipate monomer of BEPD of Example 1. Otherwise, the long chain branching can also be included by addition of 20 to 120 ppm of trimethylol propane. To remove the moisture from the reaction, the reactants are dried in a nitrogen environment at 80 ° C under vacuum. After the waste water was reduced to < 100 ppm, the vacuum was discontinued and the temperature was raised to 120 ° C, charged with an adequate amount of a metal carboxylate catalyst and then the temperature was increased to obtain a temperature of the material > 140 ° C. The reaction was maintained at the temperature until the percent of residual monomer e-caprolactone was < 1%. The polymer was discharged and converted into granules for extrusion in blown film. The melt index, the GPC molecular weight and the RSI values of the polymer were determined.
EXAMPLE 3 PREPARATION OF BRANCHED SUCCINATQ MQNQMERQ As an example of branching incorporation using other branching agents, a branched hexanediol ethyl methyl succinate monomer ("HDEMS") was prepared by reacting 2-ethyl-2-methylsuccinic acid with 1,6-hexanediol. A procedure practically similar to that described in Example 1 was followed, except that the reaction was discontinued when the acid number was about 10. An HDEMS having an acid number of 10.1 and molecular weights GPC of Mn 7628, Mw 22040, Mw / Mn 2.90 was obtained.
EXAMPLE 4 PREPARATION OF SÜCC-INATQ C-QPQLÍMERQS GAPROLACTQNA RAMIFIED HDEM A procedure practically similar to the one described in Example 2 was followed to prepare caprolactone / HDEMS copolymers. On a molar basis, the reactor was charged with the appropriate amount of monomer e-caprolactone and HDEMS monomer of Example 3. Upon completion of the reaction, the polymer was discharged and converted into extrusions for extrusion into blown film. The fusion index and the molecular weight GPC were determined.
EXAMPLE 5 PREPARATION OF BDQ ADIPATQ MQNQMERQ A procedure practically similar to that described in Example 1 was followed to prepare a butanediol adipate monomer ("BDO"), except that the reaction was discontinued when the acid number was < 10. A BDO adipate having an acid number of 8.9 and molecular weights GPC of Mn 12000, Mw 38395, Mw / Mn 3.20 was obtained. EXAMPLE 6 PREPARATION OF ADIPATQ CQPQLÍMERQ BDQ LINEAR CAPRQLAC-TQNA A procedure practically similar to that described in Example 2 was followed to prepare a copolymer caprolactone / butanediol adipate. On a molar basis, the reactor was charged with the appropriate amount of the monomer e-caprolactone and butanediol adipate monomer of Example 5. The polymer was discharged and converted into granules for extrusion into blown film. The fusion index and the molecular weight GPC were determined.
EXAMPLE CONTROL 7 PREPARATION OF PQLIQL CAPRQLAC-TQNA INITIATED WITH BUTANQDIQL A procedure practically similar to that described in Example 2 was followed to prepare a caprolactone polyol initiated by butanediol. A polyol having an acid number of 0.17 and a hydroxyl number of 22.10 was obtained. The molecular weight of the polyol based on its hydroxyl number was 5077.
EXAMPLE CONTROL 8 PREPARATION OF PQLIQL CAPRQLACTQNA INITIATED WITH BUTANQDIQL AND
ADIPOYL CHLORIDE The caprolactone polyol initiated with butanediol of Example 7 was reacted with adipoyl chloride in a 4-neck resin kettle equipped with a Dean Stark condenser and trap, stirrer and thermocouple to maintain control of a silicone oil bath . The reactor was maintained under an inert nitrogen atmosphere using a double tube gas manifold connected in parallel to an airless oil sparger. Vacuum was applied using the same collector connected in parallel to a high vacuum Welch pump. The polyol was charged to the reactor and placed under a nitrogen atmosphere. Anhydrous 1,2-dichloroethane was introduced into the reactor to facilitate separation of the water from the polyol and the temperature was raised to 120 ° C. When the water was of < 10 ppm Adipoyl chloride was added to the reactor from a clean, dry syringe. The reaction mixture begins to foam, indicating a rapid evolution of gaseous hydrogen chloride ("HCL"). After 5 minutes, a nitrogen spray tube was introduced into the reactor and the upper part of the reactor was opened to the atmosphere to facilitate the ventilation of the HCL gas. After an additional 5 minutes, solvent removal was initiated by continuous filling and draining of the Dean Stark trap distillate. The temperature of the oil bath was slowly raised to 200 ° C and maintained for 1 hour under vacuum of < 10 mm Hg. After 1 hour, the bath temperature was lowered to 160 ° C while maintaining the vacuum for 15 hours. The product was discharged and its melt flow was determined.
EXAMPLE 9 PREPARATION OF PQLIQL CAPRQLACTQNA INITIATED WITH BEPD A procedure practically as described in Example 2 was followed to prepare a caprolactone polyol initiated with BEPD. A polyol with a hydroxyl number of 22 was obtained. The molecular weight of the polyol based on its hydroxyl number was 5100.
EXAMPLE 10 PREPARATION OF PQLIQL CAPRQLACTQNA INITIATED C-QN BEPD AND CLIPRUIDE OF ADIPQILQ A procedure practically similar to that described in Example 8 was followed to react the caprolactone polyol initiated with BEPD of Example 9 with adipoyl chloride. Upon completion the product was discharged and its fluidity in the molten state was determined
EXAMPLE 11 PREPARATION OF COPOLYMER e-CAPROLACTONE / t-BUTILCAPROLACTONE
T-butylcaprolactone was obtained by performing the Baeyer Villiger reaction on 4-t-butylcyclohexanone, the details of which are known to those skilled in the art. A procedure substantially similar to that described in Example 2 was followed to prepare copolymers of e-caprolactone / t-butylcaprolactone. Typically, the reactor was charged with 95 mol% e-caprolactone and 5 mol% t-buticaprolactone. After the polymers were discharged, their melting index and GPC molecular weight were determined.
EXAMPLE 12 BIQDEGRADABILITY TEST The biodegradability of the caprolactone copolymer initiated with BEPD adipate of Example 2 was determined from the theoretical percent CO 2 produced using the standard test method ASTM D-5338. A cellulose control was used and the samples were run in duplicate.
Net theoretical C02 Days cellulose copolymer adipate BEPD 1 1.46% 3.16% 3 25.37% 13.75% 5 50.03% 21.15% 10 70.04% 43.50% 15 77.15% 75.86% 20 84.00% 93.52%
EXAMPLE 13 PREPARATION OF COMPOUNDS AND BLOWED FILM Composition The mixtures that were extruded in blown film were composed in a Brabender Prep. -Center® equipped with four heating zones; a double-screw extruder D6 / 2 of 42 mm having rotary counter propellers, constant take in a length / diameter ratio (L / D) of 7: 1; and a granulation nozzle. Upon exiting the extruder, the composite strands were passed through a water bath maintained at 10 ° C, dried by an air knife and granulated. The operating parameters were: Zone temperature: zones 1 to 4 150 ° to 180 ° C Nozzle temperature: 150 ° to 180 ° C Melt temperature: 160 ° to 190 ° C Propeller speed 75 rpm
Blown film Composite polymers and pure polymers were converted into blown film using the Brabender Prep. -Center® or a line of Sterling blown film. The Brabender Prep. -Center® was equipped with a 0.75 inch ventilated single-screw extruder with a 25: 1 L / D and a compression ratio of 2: 1, fitted with a 2-inch blown film nozzle equipped with a ring 2-inch Brabender single-coil air with cooled air. Cooperating parameters were: Zone temperature: zones 1 to 4 150 ° -180 ° C Nozzle temperature: 150 ° -180 ° C Melt temperature: 130 ° -180 ° C Propeller speed 25 rpm Caliber: 1 -1.5 mils
The Sterling blown film line was equipped with a 1.5-inch single-helix linear low density polyethylene propeller having a L: D of 24: 1, adapted with a 3-inch nozzle, 40-mils nozzle spaces and 80 mils and a 3-inch Sano, double-arm air ring with cooled air. The operating parameters were: Zone temperature: zones 1 to 4 85 ° -110 ° C Nozzle temperature: 95 ° -110 ° C Melt temperature: 95 ° -120 ° C Nozzle speed 1.40 Ib / hr- in caliber: 1-1.5 mils
EXAMPLE 1 RSI EVALUATION OF POLYMERS The BEPD adipate polymers prepared according to the procedure set forth in Example 2 were compressed into plates for evaluation. The polymers of the present invention have unique rheological properties that suggest a different molecular structure and impart better stiffness in manufactured blown films. These unique rheological properties also favor the relative ease of fabrication in finished products, especially in the extrusion of films. In particular, these polymers have melting indices (MI) and indices of the relaxation spectrum
(RSI) such that, for a given polymer, they are approximately 4.0 < (RSI) (MI 0. "54). <Approximately 15.0, or approximately 4.0 <RSI <30.0, more preferably close to 4.2 -? (RSI) (MI ') <approximately 10.0 or approximately 4.2 < RSI < 25.0 In the above formulas, MI is the polymer melt index reported as grams per 10 minutes determined according to ASTM D-1238, condition B, at 125 ° C and 2.16 kg, and the RSI is in units without dimension, measured at 75 ° C . To compare similar polymers having different melting indices, the RSI is normalized according to the previous RSI-MI relationship, where the 0.54 exponential was determined experimentally. The following examples demonstrate that the incorporation of short chain branches increases the RSI through the broadening of the molecular weight distribution. The addition of SCB and LCB also increases the RSI. The TONE® Polymer P-787 is the control and designated as Example 14-a, this increase in the RSI is not only observed in the homopolymers shown in Examples 14b-g, but also in Example 14-h a composite polymer . Example 14-h is a composite mixture of TONE® Polymer P-3% VII linear polymer of Mn 10,000), a branched PCL copolymer which can not be converted to film and the co-polymer of example 15-c.
EXAMPLE 14 EFFECTS OF THE AMPLFO BRANCHED DIQL BLOCK ON THE
PROPERTIES OF THE FILM The BEPD adipate copolymers prepared according to Example 2 were converted to film in the Brabender using the conditions delineated in the Example
13. The addition of SCB in the main chain of the adipate prepolymer gives rise to an amorphous adipate block that improves the stiffness properties of the film, such as the Elmendorf MD tear strength (MDET) and TD tensile strength. (TDTI). In addition, a more balanced film is obtained when measured by the MD / TD tensile strength resistance ratio. The following table shows the improved stiffness properties as a result of the incorporation of SCB and LCB. Compared to Example 15-a, the control TONE® Polymer P-787, the Elmendorf MD tear strength improves and in many cases the TDET also improves. Once again it was observed that rigidity can be improved by mixing as shown in Example 15-1, which has the same composition as Example 14-h.
EXAMPLE 15 PROPERTIES OF THE STERLING FILM The BEPD adipate copolymers prepared in Example 2 were converted into a film in the Sterling line, according to the procedure mentioned in Example 13. In comparison with the TONE P787 control, the improvements were observed for the TD tensile shock resulting in a more balanced film as measured by the ratio of tensile shock and MD / TD tensile strength. The resistance to the fall of the dart and the perforation of the copolymer films were significantly improved, the resistance to tearing MD was improved and the stiffness of the film was reduced as observed by the lower secant modulus.
EXAMPLE 16 EFFECT OF THE AMORFO DIQL AND LCB BLOCK ON DENSITY The density of the polymers produced as described in Example 2 was determined. The addition of a block of BEPD adipate alone or in combination with long chain branching, by the addition of TMP, gave rise to copolymers with lower density. POLYMER DENSITY (g / cc) TONE P787 1.136 COPOLYMER OF ADIPATE B? PD 1.128 COPOLYMER OF ADIPATE BEPD / TMP. xi n.i
EXAMPLE 17 PROPERTIES OF THE BRABENDER HDEMS FILM The HDEMS copolymers prepared according to Example 4 were converted to film in the Brabender using the conditions mentioned in Example 13. Compared with TONE P787, films were obtained with shock to the MD traction and puncture resistance significantly improved.
COMPARATIVE EXAMPLE 18 ADIPATQ BDO SEMICRISTALINO, LINEAR CQPQLÍMERQ MOVIE
By comparison with branched, amorphous BEPD adipate copolymers, a linear semicrystalline caprolactone copolymer was prepared as mentioned in Example 6 and made into a film in the Brabender using the conditions mentioned in Example 13. the semicrystalline block produced by the butanediol adipate monomer gave rise to a polymer with lower tear resistance, tensile shock and puncture resistance compared to the polymers of Example 2.
EXAMPLE 19 INFLUENCE OF THE BLOCKS ON THE FUSION POINT AND
CRYSTALLINITY OF THE COPOLYMER The caprolactone polyols are initiated with BDQ (Example 7) or BEPD (Example 9) and the chain was extended with adipoyl chloride as described in Examples 8 and 10, respectively. The DSC shows that compared to the TONE P787 control, the melting point, the crystallization temperature (Te), and the crystallinity are significantly reduced by the inclusion of the amorphous BEPD block. The semicrystalline BDO block gave rise to an increase in Te. It was found that the semicrystalline BDPO block provides poor film properties.
EXAMPLE 20 BRANCHED CAPROLACTONE INFLUENCE ON THE POINT OF
FUSION AND CRYSTALLINATION The s-caprolactone / t-butylcaprolactone copolymer prepared as described in Example 11 was compared to TONE P767 by DSC. The inclusion of the branched caprolactone monomer gave rise to a reduction in melting temperature, crystallinity and crystallization temperature.
In addition to the specific aspects of the present invention described herein, those skilled in the art will recognize that other aspects will be within the scope of the invention.
Claims (17)
1. A biodegradable lactone copolymer, polymerized from: (a) a first lactone monomer; and (b) a second amorphous monomer that is copolymerizable with the first monomer: characterized in that the second monomer is effective to eliminate the crystallinity of the copolymer.
2. The copolymer of claim 1, wherein the first lactone monomer is selected from the group consisting of: e-caprolactone, t-butylcaprolactone, zeta-enantolactone, delta-valerolactones, alkyl-delta-valerolactones, alkyl-epsilon- caprolactones, oxepan-2-ones, beta-lactones, gamma-lactones, dilactones, dilactides, glycolides, ketodioxanones and mixtures thereof.
3. The copolymer of claim 1 wherein the first monomer is selected from the group consisting of capralactone and derivatives thereof.
The copolymer of claim 1, wherein the second monomer is effective to initiate the polymerization of the first monomer
5. The copolymer of claim 1, wherein the second monomer is adipate ester.
6. The copolymer of claim 1, wherein the adipate ester is adipate of 2-butyl-2-ethyl-l, 3-propane.
The copolymer of claim 1, wherein the second monomer is effective to introduce amorphous regions into the copolymer.
8. The copolymer of claim 1, wherein the second monomer is effective to introduce branching into the copolymer.
9. The copolymer of claim 1, wherein the second monomer is a prepolymer with a molecular weight of from about 5QQ to 25,000 g / gmol.
The copolymer of claim 1 which is polymerized from about 99 to 80% by weight of the first monomer and from about 1 to 20% by weight of the second monomer.
11. The copolymer of claim 1, wherein the copolymer has a depression at the crystallization temperature of at least about 2 ° C.
12. The copolymer of claim 1 which has a reduction in density of at least about 0.004 g / cc.
13. A film prepared from the copolymer of claim 1.
14. The film of claim 13 having a puncture resistance from about 3 to 50 in-Ibs / mil.
15. The film of claim 13 having a dart drop of at least 50 g / mil.
16. A method for improving the stiffness of a film, the method is to use the polymer of claim 1 to manufacture the film.
17. A process for making a copolymer consists in polymerizing a first lactone monomer with a second amorphous monomer effective to eliminate the crystallinity of the copolymer. From 99 to 80% by weight of the first monomer and from about 1 to 20% by weight of the second monomer.
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US60/056,801 | 1997-08-25 |
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