USH1169H - Polymer with improved barrier properties - Google Patents
Polymer with improved barrier properties Download PDFInfo
- Publication number
- USH1169H USH1169H US07/748,403 US74840391A USH1169H US H1169 H USH1169 H US H1169H US 74840391 A US74840391 A US 74840391A US H1169 H USH1169 H US H1169H
- Authority
- US
- United States
- Prior art keywords
- polymer
- poly
- vinylidene fluoride
- polyketone
- ethylenically unsaturated
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 81
- 230000004888 barrier function Effects 0.000 title claims abstract description 15
- -1 poly(vinylidene fluoride) Polymers 0.000 claims abstract description 64
- 229920002981 polyvinylidene fluoride Polymers 0.000 claims abstract description 32
- 238000000034 method Methods 0.000 claims abstract description 19
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 18
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims abstract description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 230000005540 biological transmission Effects 0.000 claims abstract description 5
- 230000035699 permeability Effects 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 7
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 7
- 239000000203 mixture Substances 0.000 abstract description 40
- 239000011872 intimate mixture Substances 0.000 abstract description 2
- 229920001470 polyketone Polymers 0.000 description 46
- 229920001897 terpolymer Polymers 0.000 description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 9
- 239000005977 Ethylene Substances 0.000 description 9
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical group [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 6
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- 150000001450 anions Chemical class 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical group FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 239000003446 ligand Substances 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- SXXPTCXIFIOPQF-UHFFFAOYSA-N 3-bis(2-methoxyphenyl)phosphanylpropyl-bis(2-methoxyphenyl)phosphane Chemical compound COC1=CC=CC=C1P(C=1C(=CC=CC=1)OC)CCCP(C=1C(=CC=CC=1)OC)C1=CC=CC=C1OC SXXPTCXIFIOPQF-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 3
- LVEYOSJUKRVCCF-UHFFFAOYSA-N 1,3-bis(diphenylphosphino)propane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)CCCP(C=1C=CC=CC=1)C1=CC=CC=C1 LVEYOSJUKRVCCF-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 2
- 229920006370 Kynar Polymers 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920003298 Nucrel® Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 235000013361 beverage Nutrition 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 150000002941 palladium compounds Chemical class 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- BYYLJVQCWRRFMP-UHFFFAOYSA-N 1-ethenyl-3-propan-2-ylbenzene Chemical compound CC(C)C1=CC=CC(C=C)=C1 BYYLJVQCWRRFMP-UHFFFAOYSA-N 0.000 description 1
- WHFHDVDXYKOSKI-UHFFFAOYSA-N 1-ethenyl-4-ethylbenzene Chemical compound CCC1=CC=C(C=C)C=C1 WHFHDVDXYKOSKI-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000009970 fire resistant effect Effects 0.000 description 1
- 238000009459 flexible packaging Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000012803 melt mixture Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920000131 polyvinylidene Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L73/00—Compositions of macromolecular compounds obtained by reactions forming a linkage containing oxygen or oxygen and carbon in the main chain, not provided for in groups C08L59/00 - C08L71/00; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/16—Homopolymers or copolymers or vinylidene fluoride
Definitions
- This invention relates to polyketone polymers, and, more particularly, to compositions of a polyketone polymer blended with a poly(vinylidene fluoride) which exhibit improved barrier properties.
- Processes for production of the polyketone polymers typically involve the use of a catalyst composition formed from a compound of a Group VIII metal selected from palladium, cobalt or nickel, the anion of a strong non-hydrohalogenic acid and a bidentate ligand of phosphorus, arsenic or antimony.
- U.S. Pat. No. 4,843,144 discloses a process for preparing polymers of carbon monoxide and at least one ethylenically unsaturated hydrocarbon using a catalyst comprising a compound of palladium, the anion of a non-hydrohalogenic acid having a pKa of below about 6, and a bidentate ligand of phosphorus.
- the resulting polymers are relatively high molecular weight materials having utility as thermoplastics in the production of shaped articles, such as containers for food and beverages and film for packaging. In order to improve the utility of such shaped articles, it would be desirable to improve the barrier properties of the polyketone polymers.
- the present invention provides a method for improving the barrier properties of linear alternating polymers of carbon monoxide and at least one ethylenically unsaturated hydrocarbon (i.e. polyketone polymers) by incorporating therein a poly(vinylidene fluoride) polymer.
- the resulting blends demonstrate reduced permeability to water vapor.
- the present invention also provides shaped articles, such as containers and films, manufactured from a blend of a polyketone polymer and a poly(vinylidene fluoride)polymer.
- the polyketone polymers of the invention are of a linear alternating structure and contain substantially one molecule of carbon monoxide for each molecule of unsaturated hydrocarbon.
- Suitable ethylenically unsaturated hydrocarbons for use as precursors of the polyketone polymers have up to 20 carbon atoms inclusive, preferably up to 10 carbon atoms, and are aliphatic such as ethylene and other ⁇ -olefins including propylene, 1-butene, isobutylene, 1-hexene, 1-octene and 1-dodecene, or are arylaliphatic containing an aryl substituent on an otherwise aliphatic molecule, particularly an aryl substituent on a carbon atom of the ethylenic unsaturation.
- Illustrative of this latter class of ethylenically unsaturated hydrocarbons are styrene, p-methylstyrene, p-ethylstyrene and m-isopropylstyrene.
- the preferred polyketone polymers are copolymers of carbon monoxide and ethylene or terpolymers of carbon monoxide, ethylene and a second ethylenically unsaturated hydrocarbon of at least 3 carbon atoms, particularly an ⁇ -olefin such as propylene.
- the preferred polyketone terpolymers When the preferred polyketone terpolymers are employed as the major polymeric component of the blends of the invention, there will be within the terpolymer at least about 2 units incorporating a moiety of ethylene for each unit incorporating a moiety of the second hydrocarbon. Preferably, there will be from about 10 units to about 100 units incorporating a moiety of ethylene for each unit incorporating a moiety of the second hydrocarbon.
- the polymer chain of the preferred polyketone polymers is therefore represented by the repeating formula ##STR1## wherein G is the moiety of ethylenically unsaturated hydrocarbon of at least 3 carbon atoms polymerized through the ethylenic unsaturation and the ratio of y:x is no more than about 0.5.
- polyketone polymers of number average molecular weight from about 1000 to about 200,000, particularly those of number average molecular weight from about 20,000 to about 90,000 as determined by gel permeation chromatography.
- the physical properties of the polymer will depend in part upon the molecular weight, whether the polymer is a copolymer or a terpolymer and, in the case of terpolymers, the nature and proportion of the second hydrocarbon present.
- Typical melting points for the polymers are from about 175° C. to about 300° C., more typically from about 210° C. to about 270° C.
- the polymers have a limiting viscosity number (LVN), measured in m-cresol at 60° C. in a standard capillary viscosity measuring device, from about 0.5 dl/g to about 10 dl/g, more frequently from about 0.8 dl/g to about 4 dl/g.
- LPN limiting viscosity number
- a preferred method for the production of the polyketone polymers is illustrated by U.S. Pat. No. 4,843,144 (Van Broekhoven et al.).
- the carbon monoxide and hydrocarbon monomer(s) are contacted under polymerization conditions in the presence of a catalyst composition formed from a compound of palladium, the anion of a non-hydrohalogenic acid having a pKa (measured in water at 18° C.) of below about 6, preferably below 2, and a bidentate ligand of phosphorus.
- a preferred palladium compound is a palladium carboxylate, particularly palladium acetate
- a preferred anion is the anion of trifluoroacetic acid or p-toluenesulfonic acid
- a preferred bidentate ligand of phosphorus is 1,3-bis(diphenylphosphino)propane or 1,3-bis[di(2-methoxyphenyl)phosphino]propane.
- the polymerization to produce the polyketone polymer is conducted in an inert reaction diluent, preferably an alkanolic diluent, and methanol is preferred.
- the reactants, catalyst composition and reaction diluent are contacted by conventional methods such as shaking, stirring or refluxing in a suitable reaction vessel.
- Typical polymerization conditions include a reaction temperature from about 20° C. to about 150° C., preferably from about 50° C. to about 135° C.
- the reaction pressure is suitable from about 1 atmosphere to about 200 atmospheres but pressures from about 10 atmospheres to about 100 atmospheres are preferred.
- the reaction is terminated as by cooling the reactor and contents and releasing the pressure.
- the polyketone polymer is typically obtained as a product substantially insoluble in the reaction diluent and the product is recovered by conventional methods such as filtration or decantation.
- the polyketone polymer is used as recovered or the polymer is purified as by contact with a solvent or extraction agent which is selective for catalyst residues.
- the polymer utilized to improve the barrier properties of the polyketone polymers is a poly(vinylidene fluoride) polymer.
- poly(vinylidene fluoride) polymer is meant a polymer wherein at least a considerable predominance of the monomer units present is vinylidene fluoride, represented by the formula CH 2 ⁇ CF 2 .
- the polyvinylidene polymer is a homopolymer of vinylidene fluoride.
- copolymers of at least 90% by mole of vinylidene fluoride are suitable, with any remainder being other fluorinated monomeric moieties containing fluorine, such as tetrafluoroethylene, hexafluoropropylene or vinyl fluoride.
- polyvinylidene fluoride polymers are well known in the art and are produced, for example, by conventional methods such as those described in U.S. Pat. No. 2,435,537 (Ford et al.) and U.S. Pat. No. 3,031,437 (Iserson).
- the poly(vinylidene fluoride) polymers are thermoplastic in character, having softening temperatures on the order of 145° C., and are conventionally used in films and coatings.
- Such polymers are commercially available, e.g. Atochem KYNAR® 201.
- the method of the invention comprises incorporating into a polyketone polymer an amount of the poly(vinylidene fluoride) polymer effective to improve the barrier properties of the polyketone polymer.
- the specific amount of poly(vinylidene fluoride) and the relative proportions of the two components of the blend is not critical, as long as an effective amount is present and other important polymer properties for the intended use are not adversely affected.
- the poly(vinylidene fluoride) is provided in an amount from about 10 wt. % to about 45 wt. % poly(vinylidene fluoride), based on the total weight of polymer. Compositions containing from about 25 wt. % to about 45 wt.
- compositions containing from about 35 wt. % to about 45 wt. % poly(vinylidene fluoride) are preferred for a wide variety of packaging applications.
- the polyketone/poly(vinylidene fluoride) polymer blend is a non-miscible blend, with the poly(vinylidene fluoride) polymer existing as a discrete phase in the polyketone matrix with a phase size on the order of from about 0.8 micron to about 2.2 microns, more often on the order of from about 1.2 micron to about 1.6 micron.
- the blends will not be homogeneous, but satisfactory blends are obtained when the poly(vinylidene fluoride) is uniformly distributed throughout the polyketone matrix.
- compatibility of the polyketone/poly(vinylidene fluoride) blends is due to hydrogen bonding of the ketones on the polyketone polymer with the methylene hydrogens of the poly(vinylidene fluoride) polymer in the vicinity of the interface of the component domains.
- the poly(vinylidene fluoride) is added to the polyketone polymer by any method suitable for forming an intimate mixture of the two polymers. Such methods include dry blending of the polymers in a finely divided form, followed by injection molding or extrusion of the mixture using single or twin screw extruders.
- the composition may also be produced by blending the components in a melt mixing device. In general, subjecting the melt mixture to a high shear field for some period is necessary to generate the desired dispersion.
- compositions of the invention may also include other additives such as antioxidants, dyes, fillers or reinforcing agents, fire resistant materials, mold release agents, colorants and other materials designed to improve the processability of the polymers or the properties of the resulting blend.
- additives are added prior to, together with, or subsequent to the blending of the polyketone and poly(vinylidene fluoride).
- compositions are processed by methods such as extrusion and injection molding into sheets, films, plates, containers and other shaped articles.
- Illustrative of desirable applications are the production of articles useful in both rigid and flexible packaging applications for food, beverages, and other materials.
- a linear alternating terpolymer of carbon monoxide, ethylene, and propylene (P-1000/2) was produced in the presence of a catalyst composition formed from palladium acetate, trifluoroacetic acid and 1,3-bis[di(2-methoxyphenyl)phosphino]propane.
- the polyketone polymer had a melting point of about 220° C. and an LVN of about 1.8 dl/g when measured in m-cresol at 60° C.
- the polyketone polymer also contained 0.5% Ethanox 330 and 0.5% Nucrel 535.
- Blends were prepared of the polyketone terpolymer of Example 1 and an extrusion grade poly(vinylidene fluoride), KYNAR 201, available from Atochem Corporation. The blends were compounded using a Haake 30 mm co-rotating twin screw extruder operating at 250° C. and 200 rpm, and subsequently injection molded using an Arburg Allrounder. Molded specimens were used for mechanical testing.
- the mechanical properties of the polyketone/poly(vinylidene fluoride) blends are summarized in Table 1.
- the strength and stiffness of the polyketone matrix are almost fully maintained upon blending with up to 40 wt. % poly(vinylidene fluoride).
- the blends also maintain a high level of ductility and toughness, as indicated by elongations at break greater than 200%, and notched Izod impact values greater than 3.0 ft-lb/in.
- the permeability properties of the blends are also summarized in Table 1.
- a Mocon cell using a modulated infrared sensor (ASTM F 1249) was used to determine the permeability to water vapor at 100° F. and 90% relative humidity for compression molded plaques that were 30 mils thick.
- the permeability decreased approximately linearly with increasing proportion of poly(vinylidene fluoride).
- a linear alternating terpolymer of carbon monoxide, ethylene, and propylene (89/054) was produced in the presence of a catalyst composition formed from palladium acetate, trifluoroacetic acid and 1,3-bis[di(2-methoxyphenyl)phosphino]propane.
- the polyketone polymer had a melting point of about 220° C. and an LVN of about 1.1 dl/g when measured in m-cresol at 60° C.
- the polyketone polymer also contained 0.5% Ethanox 330 and 0.5% Nucrel 535.
- Blends were prepared of the polyketone terpolymer of Example 3 and the poly(vinylidene fluoride) of Example 2.
- the blends were compounded using a Haake 30 mm co-rotating twin screw extruder operating at 250° C. and 200 RPM, and subsequently injection molded into 7.5 oz. cups using a Krauss-Maffei 100-ton injection molding machine.
- the cups had an average wall thickness of about 27 mils.
- the cups were filled with water, double seamed with an aluminum lid, maintained in a 50% relative humidity environment, and weighed periodically to determine water loss over time. Some of the samples were also subjected to a retort cycle in a Barnstead benchtop sterilization unit with 15 psi overpressure. The retort temperature was increased until the internal temperature reached 260° F., at which point the container was slowly cooled to 150° F. The total cycle required about three hours.
- the water vapor transmission rates for these containers are shown in Table 2.
- the rate of weight loss decreased approximately linearly with increasing proportion of poly(vinylidene fluoride).
- the containers subjected to a retort cycle demonstrated about 40% increase in the rate of water loss through the container, relative to the samples not subjected to the retort cycle.
- the fact that the blends did not experience a greater increase in water transport rate than the unblended polyketone control as a result of retort "shock" is additional evidence of good blend compatibility.
- the cups which were molded from the blends of this example maintained an excellent appearance, as evidenced particularly by a lack of splay, delamination, or surface blemishes.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Polymer compositions comprising an intimate mixture of a linear alternating polymer of carbon monoxide and at least one ethylenically unsaturated hydrocarbon and a poly(vinylidene fluoride) exhibit improved barrier properties. The poly(vinylidene fluoride) is also useful in a method of reducing the water vapor transmission rate of a linear alternating polymer of carbon monoxide and at least one ethylenically unsaturated hydrocarbon.
Description
This invention relates to polyketone polymers, and, more particularly, to compositions of a polyketone polymer blended with a poly(vinylidene fluoride) which exhibit improved barrier properties.
The class of polymers of carbon monoxide and olefins has been known for some time. U.S. Pat. No. 2,495,286 (Brubaker) discloses such polymers of relatively low carbon monoxide content produced in the presence of free radical initiators, e.g., peroxy compounds. G.B. 1,081,304 discloses similar polymers of higher carbon monoxide content produced in the presence of alkylphosphine complexes of palladium compounds as catalyst. U.S. Pat. No. 3,694,412 (Nozaki) extended the reaction to produce linear alternating polymers in the presence of arylphosphine complexes of palladium moieties and certain inert solvents.
More recently, the class of linear alternating polymers of carbon monoxide and at least one ethylenically unsaturated hydrocarbon, now becoming known as polyketones or polyketone polymers, has become of greater interest. U.S. Pat. No. 4,880,903 (VanBroekhoven et al.) discloses a linear alternating polyketone terpolymer of carbon monoxide, ethylene, and other olefinically unsaturated hydrocarbons, such as propylene. Processes for production of the polyketone polymers typically involve the use of a catalyst composition formed from a compound of a Group VIII metal selected from palladium, cobalt or nickel, the anion of a strong non-hydrohalogenic acid and a bidentate ligand of phosphorus, arsenic or antimony. U.S. Pat. No. 4,843,144 (VanBroekhoven et al.) discloses a process for preparing polymers of carbon monoxide and at least one ethylenically unsaturated hydrocarbon using a catalyst comprising a compound of palladium, the anion of a non-hydrohalogenic acid having a pKa of below about 6, and a bidentate ligand of phosphorus.
The resulting polymers are relatively high molecular weight materials having utility as thermoplastics in the production of shaped articles, such as containers for food and beverages and film for packaging. In order to improve the utility of such shaped articles, it would be desirable to improve the barrier properties of the polyketone polymers.
The present invention provides a method for improving the barrier properties of linear alternating polymers of carbon monoxide and at least one ethylenically unsaturated hydrocarbon (i.e. polyketone polymers) by incorporating therein a poly(vinylidene fluoride) polymer. The resulting blends demonstrate reduced permeability to water vapor. The present invention also provides shaped articles, such as containers and films, manufactured from a blend of a polyketone polymer and a poly(vinylidene fluoride)polymer.
It is an object of this invention to improve the barrier properties of polyketone polymers to enhance their utility for packaging food and other materials. This object is realized by adding a blend component with barrier properties better than those of a polyketone polymer to the polyketone polymer. Other objects will be apparent from the description of the invention.
U.S. Pat. No. 4,818,786 (Gergen et al.) discloses that the addition of a poly(vinylidene fluoride) to a polyketone polymer results in an immiscible blend of useful properties. Such blends exhibit a favorable degree of compatibility between the two blend components, and demonstrate good mechanical properties.
It has now been found that these blends exhibit good barrier properties, and provide a method for improving the barrier properties of a polyketone polymer while maintaining other important properties, notably stiffness, strength, and toughness.
The polyketone polymers of the invention are of a linear alternating structure and contain substantially one molecule of carbon monoxide for each molecule of unsaturated hydrocarbon. Suitable ethylenically unsaturated hydrocarbons for use as precursors of the polyketone polymers have up to 20 carbon atoms inclusive, preferably up to 10 carbon atoms, and are aliphatic such as ethylene and other α-olefins including propylene, 1-butene, isobutylene, 1-hexene, 1-octene and 1-dodecene, or are arylaliphatic containing an aryl substituent on an otherwise aliphatic molecule, particularly an aryl substituent on a carbon atom of the ethylenic unsaturation. Illustrative of this latter class of ethylenically unsaturated hydrocarbons are styrene, p-methylstyrene, p-ethylstyrene and m-isopropylstyrene. The preferred polyketone polymers are copolymers of carbon monoxide and ethylene or terpolymers of carbon monoxide, ethylene and a second ethylenically unsaturated hydrocarbon of at least 3 carbon atoms, particularly an α-olefin such as propylene.
When the preferred polyketone terpolymers are employed as the major polymeric component of the blends of the invention, there will be within the terpolymer at least about 2 units incorporating a moiety of ethylene for each unit incorporating a moiety of the second hydrocarbon. Preferably, there will be from about 10 units to about 100 units incorporating a moiety of ethylene for each unit incorporating a moiety of the second hydrocarbon. The polymer chain of the preferred polyketone polymers is therefore represented by the repeating formula ##STR1## wherein G is the moiety of ethylenically unsaturated hydrocarbon of at least 3 carbon atoms polymerized through the ethylenic unsaturation and the ratio of y:x is no more than about 0.5. When copolymers of carbon monoxide and ethylene are employed in the blends of the invention, there will be no second hydrocarbon present and the copolymers are represented by the above formula wherein y is zero. When y is other than zero, i.e. terpolymers are employed, the --CO--CH2 CH2 -- units and the --CO--G-- units are found randomly throughout the polymer chain, and preferred ratios of y:x are from about 0.01 to about 0.1. The end groups or "caps" of the polymer chain will depend upon what materials were present during the production of the polymer and whether or how the polymer was purified. The precise nature of the end groups does not appear to influence the properties of the polymer to any considerable extent so that the polymers are fairly represented by the formula for the polymer chain as depicted above.
Of particular interest are the polyketone polymers of number average molecular weight from about 1000 to about 200,000, particularly those of number average molecular weight from about 20,000 to about 90,000 as determined by gel permeation chromatography. The physical properties of the polymer will depend in part upon the molecular weight, whether the polymer is a copolymer or a terpolymer and, in the case of terpolymers, the nature and proportion of the second hydrocarbon present. Typical melting points for the polymers are from about 175° C. to about 300° C., more typically from about 210° C. to about 270° C. The polymers have a limiting viscosity number (LVN), measured in m-cresol at 60° C. in a standard capillary viscosity measuring device, from about 0.5 dl/g to about 10 dl/g, more frequently from about 0.8 dl/g to about 4 dl/g.
A preferred method for the production of the polyketone polymers is illustrated by U.S. Pat. No. 4,843,144 (Van Broekhoven et al.). The carbon monoxide and hydrocarbon monomer(s) are contacted under polymerization conditions in the presence of a catalyst composition formed from a compound of palladium, the anion of a non-hydrohalogenic acid having a pKa (measured in water at 18° C.) of below about 6, preferably below 2, and a bidentate ligand of phosphorus. The scope of the polymerization is extensive but, without wishing to be limited, a preferred palladium compound is a palladium carboxylate, particularly palladium acetate, a preferred anion is the anion of trifluoroacetic acid or p-toluenesulfonic acid and a preferred bidentate ligand of phosphorus is 1,3-bis(diphenylphosphino)propane or 1,3-bis[di(2-methoxyphenyl)phosphino]propane.
The polymerization to produce the polyketone polymer is conducted in an inert reaction diluent, preferably an alkanolic diluent, and methanol is preferred. The reactants, catalyst composition and reaction diluent are contacted by conventional methods such as shaking, stirring or refluxing in a suitable reaction vessel. Typical polymerization conditions include a reaction temperature from about 20° C. to about 150° C., preferably from about 50° C. to about 135° C. The reaction pressure is suitable from about 1 atmosphere to about 200 atmospheres but pressures from about 10 atmospheres to about 100 atmospheres are preferred. Subsequent to polymerization, the reaction is terminated as by cooling the reactor and contents and releasing the pressure. The polyketone polymer is typically obtained as a product substantially insoluble in the reaction diluent and the product is recovered by conventional methods such as filtration or decantation. The polyketone polymer is used as recovered or the polymer is purified as by contact with a solvent or extraction agent which is selective for catalyst residues.
The polymer utilized to improve the barrier properties of the polyketone polymers is a poly(vinylidene fluoride) polymer. By poly(vinylidene fluoride) polymer is meant a polymer wherein at least a considerable predominance of the monomer units present is vinylidene fluoride, represented by the formula CH2 ═CF2. In preferred modifications the polyvinylidene polymer is a homopolymer of vinylidene fluoride. In other modifications, copolymers of at least 90% by mole of vinylidene fluoride are suitable, with any remainder being other fluorinated monomeric moieties containing fluorine, such as tetrafluoroethylene, hexafluoropropylene or vinyl fluoride. Such polyvinylidene fluoride polymers are well known in the art and are produced, for example, by conventional methods such as those described in U.S. Pat. No. 2,435,537 (Ford et al.) and U.S. Pat. No. 3,031,437 (Iserson). The poly(vinylidene fluoride) polymers are thermoplastic in character, having softening temperatures on the order of 145° C., and are conventionally used in films and coatings. Such polymers are commercially available, e.g. Atochem KYNAR® 201.
The method of the invention comprises incorporating into a polyketone polymer an amount of the poly(vinylidene fluoride) polymer effective to improve the barrier properties of the polyketone polymer. The specific amount of poly(vinylidene fluoride) and the relative proportions of the two components of the blend is not critical, as long as an effective amount is present and other important polymer properties for the intended use are not adversely affected. The poly(vinylidene fluoride) is provided in an amount from about 10 wt. % to about 45 wt. % poly(vinylidene fluoride), based on the total weight of polymer. Compositions containing from about 25 wt. % to about 45 wt. % poly(vinylidene fluoride), on the same basis, are believed to exhibit desirable barrier properties, while compositions containing from about 35 wt. % to about 45 wt. % poly(vinylidene fluoride) are preferred for a wide variety of packaging applications.
The polyketone/poly(vinylidene fluoride) polymer blend is a non-miscible blend, with the poly(vinylidene fluoride) polymer existing as a discrete phase in the polyketone matrix with a phase size on the order of from about 0.8 micron to about 2.2 microns, more often on the order of from about 1.2 micron to about 1.6 micron. The blends will not be homogeneous, but satisfactory blends are obtained when the poly(vinylidene fluoride) is uniformly distributed throughout the polyketone matrix. While not wishing to be bound by any particular theory, it is speculated that compatibility of the polyketone/poly(vinylidene fluoride) blends is due to hydrogen bonding of the ketones on the polyketone polymer with the methylene hydrogens of the poly(vinylidene fluoride) polymer in the vicinity of the interface of the component domains.
The poly(vinylidene fluoride) is added to the polyketone polymer by any method suitable for forming an intimate mixture of the two polymers. Such methods include dry blending of the polymers in a finely divided form, followed by injection molding or extrusion of the mixture using single or twin screw extruders. The composition may also be produced by blending the components in a melt mixing device. In general, subjecting the melt mixture to a high shear field for some period is necessary to generate the desired dispersion.
The compositions of the invention may also include other additives such as antioxidants, dyes, fillers or reinforcing agents, fire resistant materials, mold release agents, colorants and other materials designed to improve the processability of the polymers or the properties of the resulting blend. Such additives are added prior to, together with, or subsequent to the blending of the polyketone and poly(vinylidene fluoride).
The compositions are processed by methods such as extrusion and injection molding into sheets, films, plates, containers and other shaped articles. Illustrative of desirable applications are the production of articles useful in both rigid and flexible packaging applications for food, beverages, and other materials.
The invention is further illustrated by the following Examples which should not be regarded as limiting.
A linear alternating terpolymer of carbon monoxide, ethylene, and propylene (P-1000/2) was produced in the presence of a catalyst composition formed from palladium acetate, trifluoroacetic acid and 1,3-bis[di(2-methoxyphenyl)phosphino]propane. The polyketone polymer had a melting point of about 220° C. and an LVN of about 1.8 dl/g when measured in m-cresol at 60° C. The polyketone polymer also contained 0.5% Ethanox 330 and 0.5% Nucrel 535.
Blends were prepared of the polyketone terpolymer of Example 1 and an extrusion grade poly(vinylidene fluoride), KYNAR 201, available from Atochem Corporation. The blends were compounded using a Haake 30 mm co-rotating twin screw extruder operating at 250° C. and 200 rpm, and subsequently injection molded using an Arburg Allrounder. Molded specimens were used for mechanical testing.
The mechanical properties of the polyketone/poly(vinylidene fluoride) blends are summarized in Table 1. The strength and stiffness of the polyketone matrix are almost fully maintained upon blending with up to 40 wt. % poly(vinylidene fluoride). The blends also maintain a high level of ductility and toughness, as indicated by elongations at break greater than 200%, and notched Izod impact values greater than 3.0 ft-lb/in.
The permeability properties of the blends are also summarized in Table 1. A Mocon cell using a modulated infrared sensor (ASTM F 1249) was used to determine the permeability to water vapor at 100° F. and 90% relative humidity for compression molded plaques that were 30 mils thick. The permeability decreased approximately linearly with increasing proportion of poly(vinylidene fluoride).
TABLE 1 __________________________________________________________________________ Tensile, Impact, and Permeability Properties Composition Flexural Flexural Tensile Elongation (Polyketone/ Modulus Strength Strength at Break Notched Izod @ Gardner Impact @ Permeability PVF) (PSI) (PSI) (PSI) (%) RT (ft-lb/in) -30° C. (in-lb) (cc-mil/100 in.sup.2 __________________________________________________________________________ -day) 100/0 251,000 8690 8590 200 4.1 64 13.6 90/10 255,00 8840 8560 260 3.5 28 11.9 80/20 248,000 8720 8170 230 3.1 37 11.0 70/30 249,000 8950 8040 310 3.3 24 9.35 60/40 254,000 9020 7990 360 3.2 18 8.5 0/100 -- -- 6350 70 2.5 -- 4.9* __________________________________________________________________________ *Published data.
A linear alternating terpolymer of carbon monoxide, ethylene, and propylene (89/054) was produced in the presence of a catalyst composition formed from palladium acetate, trifluoroacetic acid and 1,3-bis[di(2-methoxyphenyl)phosphino]propane. The polyketone polymer had a melting point of about 220° C. and an LVN of about 1.1 dl/g when measured in m-cresol at 60° C. The polyketone polymer also contained 0.5% Ethanox 330 and 0.5% Nucrel 535.
Blends were prepared of the polyketone terpolymer of Example 3 and the poly(vinylidene fluoride) of Example 2. The blends were compounded using a Haake 30 mm co-rotating twin screw extruder operating at 250° C. and 200 RPM, and subsequently injection molded into 7.5 oz. cups using a Krauss-Maffei 100-ton injection molding machine. The cups had an average wall thickness of about 27 mils.
The cups were filled with water, double seamed with an aluminum lid, maintained in a 50% relative humidity environment, and weighed periodically to determine water loss over time. Some of the samples were also subjected to a retort cycle in a Barnstead benchtop sterilization unit with 15 psi overpressure. The retort temperature was increased until the internal temperature reached 260° F., at which point the container was slowly cooled to 150° F. The total cycle required about three hours.
The water vapor transmission rates for these containers are shown in Table 2. The rate of weight loss decreased approximately linearly with increasing proportion of poly(vinylidene fluoride). In all cases, the containers subjected to a retort cycle demonstrated about 40% increase in the rate of water loss through the container, relative to the samples not subjected to the retort cycle. The fact that the blends did not experience a greater increase in water transport rate than the unblended polyketone control as a result of retort "shock" is additional evidence of good blend compatibility. The cups which were molded from the blends of this example maintained an excellent appearance, as evidenced particularly by a lack of splay, delamination, or surface blemishes.
TABLE 2 ______________________________________ Water Vapor Transmission Rate for Thin-Wall Containers Composition Water Vapor Transmission Rate (Polyketone/ (% weight loss per year) PVF) Without Retort After Retort ______________________________________ 100/0 5.56 7.97 80/20 4.19 6.03 60/40 3.11 4.32 ______________________________________
The examples above demonstrate that poly(vinylidene fluoride)may be used to improve the barrier properties of a polyketone polymer.
Claims (10)
1. A method for improving barrier properties of a linear alternating polymer of carbon monoxide and at least one ethylenically unsaturated hydrocarbon by incorporating therein an amount of a poly(vinylidene fluoride) polymer sufficient to reduce the barrier property water vapor transmission rate of the linear alternating polymer to less than about 5 wt. % loss per year.
2. The method of claim 1 wherein the polymer is of the repeating formula ##STR2## wherein G is a moiety of an ethylenically unsaturated hydrocarbon of at least 3 carbon atoms polymerized through the ethylenic unsaturation, and the ratio of y:x is no more than about 0.5.
3. The method of claim 1 wherein y is 0.
4. The method of claim 1 wherein the ratio of y:x is from about 0.01 to about 0.1.
5. The method of claim 4 wherein G is a moiety of propylene.
6. A method of reducing a water vapor permeability rate of a linear alternating polymer of carbon monoxide and at least one ethylenically unsaturated hydrocarbon by incorporating therein an amount of a poly(vinylidene fluoride) sufficient to reduce the water vapor permeability rate of the linear alternating polymer to about 10 cc-mil/100 in2 -day or less.
7. The method of claim 6 wherein the polymer is of the repeating formula ##STR3## wherein G is a moiety of an ethylenically unsaturated hydrocarbon of at least 3 carbon atoms, polymerized through the ethylenic unsaturation, and the ratio of y:x is no more than about 0.5.
8. The method of claim 7 wherein y is 0.
9. The method of claim 7 wherein the ratio of y:x is from 0.01 to about 0.1.
10. The method of claim 9 wherein G is a moiety of propylene.
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US07/748,403 USH1169H (en) | 1991-08-22 | 1991-08-22 | Polymer with improved barrier properties |
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CN115725168A (en) * | 2022-11-22 | 2023-03-03 | 黄河三角洲京博化工研究院有限公司 | POK porous foam material and preparation method thereof |
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