CA2057474A1 - Process for forming paper-based products having cement-based coatings - Google Patents
Process for forming paper-based products having cement-based coatingsInfo
- Publication number
- CA2057474A1 CA2057474A1 CA002057474A CA2057474A CA2057474A1 CA 2057474 A1 CA2057474 A1 CA 2057474A1 CA 002057474 A CA002057474 A CA 002057474A CA 2057474 A CA2057474 A CA 2057474A CA 2057474 A1 CA2057474 A1 CA 2057474A1
- Authority
- CA
- Canada
- Prior art keywords
- coating composition
- paper
- product
- cement
- process defined
- 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
- 239000004568 cement Substances 0.000 title claims abstract description 35
- 238000000034 method Methods 0.000 title claims abstract description 34
- 238000000576 coating method Methods 0.000 title claims description 41
- 239000008199 coating composition Substances 0.000 claims abstract description 53
- 239000004927 clay Substances 0.000 claims abstract description 18
- 229910021653 sulphate ion Inorganic materials 0.000 claims abstract description 17
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims abstract description 16
- 239000004908 Emulsion polymer Substances 0.000 claims abstract description 15
- 238000000465 moulding Methods 0.000 claims abstract description 12
- 150000007524 organic acids Chemical class 0.000 claims abstract description 8
- 238000007731 hot pressing Methods 0.000 claims abstract description 6
- 238000001035 drying Methods 0.000 claims abstract description 5
- 239000011248 coating agent Substances 0.000 claims description 33
- 235000013305 food Nutrition 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 8
- 239000010893 paper waste Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 238000005520 cutting process Methods 0.000 claims description 2
- 238000009966 trimming Methods 0.000 claims 1
- 239000000123 paper Substances 0.000 description 56
- 239000000203 mixture Substances 0.000 description 29
- 239000000758 substrate Substances 0.000 description 27
- 239000001993 wax Substances 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 239000000839 emulsion Substances 0.000 description 12
- 239000011398 Portland cement Substances 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 8
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 239000005995 Aluminium silicate Substances 0.000 description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 235000012211 aluminium silicate Nutrition 0.000 description 6
- 239000005038 ethylene vinyl acetate Substances 0.000 description 6
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- 229920006328 Styrofoam Polymers 0.000 description 5
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000008261 styrofoam Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 239000000908 ammonium hydroxide Substances 0.000 description 4
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 4
- 239000001175 calcium sulphate Substances 0.000 description 4
- 235000011132 calcium sulphate Nutrition 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 239000013530 defoamer Substances 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000006188 syrup Substances 0.000 description 3
- 235000020357 syrup Nutrition 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 239000011111 cardboard Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 235000013410 fast food Nutrition 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N ferric oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 235000013622 meat product Nutrition 0.000 description 2
- 239000011105 molded pulp Substances 0.000 description 2
- 235000016337 monopotassium tartrate Nutrition 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 239000011087 paperboard Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- KYKNRZGSIGMXFH-ZVGUSBNCSA-M potassium bitartrate Chemical compound [K+].OC(=O)[C@H](O)[C@@H](O)C([O-])=O KYKNRZGSIGMXFH-ZVGUSBNCSA-M 0.000 description 2
- 229940086065 potassium hydrogentartrate Drugs 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 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
- 238000000429 assembly Methods 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000003413 degradative effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 229910001649 dickite Inorganic materials 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007590 electrostatic spraying Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 239000011953 free-radical catalyst Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- BDRTVPCFKSUHCJ-UHFFFAOYSA-N molecular hydrogen;potassium Chemical compound [K].[H][H] BDRTVPCFKSUHCJ-UHFFFAOYSA-N 0.000 description 1
- 239000002687 nonaqueous vehicle Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000003340 retarding agent Substances 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- CMXPERZAMAQXSF-UHFFFAOYSA-M sodium;1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate;1,8-dihydroxyanthracene-9,10-dione Chemical compound [Na+].O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=CC=C2O.CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC CMXPERZAMAQXSF-UHFFFAOYSA-M 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/64—Inorganic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Paper (AREA)
Abstract
Abstract of the Disclosure A process for forming a moulded paper product which is degradable in a moisture active landfill is disclosed. The process involves providing a paper pulped paper feedstock, moulding the feedstock to produce a shaped product, drying the shaped product, applying a coating composition on to at least one surface of the shaped product, curing the coating composition and, optionally, hot pressing the resulting product to form a moulded paper product. When the moulded paper product is coated utilizing a particularly preferred coating composition described herein, which is comprised of a cement, at least one of a clay and a sulphate, an aqueous emulsion polymer, and preferably, at least one of an organic acid and a wax, it is readily degradable in a moisture active landfill.
McCarthy Tetrault TOR-DOCS -139214
McCarthy Tetrault TOR-DOCS -139214
Description
PROCESS FOR FORMING PAPER-BASFD PRODUCTS
lH~VING C~MENT-BASED COATINGS
This invention relates to coating compositions and process for using the 5 coating compositions. More particularly, this invention relates to cemen~-containing coating compositions which can be applied to paper products and the processes for preparing and coating these products.
In recent years, increasing concerns have been expressed about the use 10 of plastic containers~ such as styrofoam cont~iners, in the food industry. Plastic containers, such as those used in grocery stores and fast food restaurants to package food, are not degradable and, as a result, are contributing to the fill-up of landfills.
In addition, when some plastic containers are manufactured or burned, harmful compounds are released into the atmosphere which cause pollution or which damage15 the ozone layer. For example, styrofoam is usually foamed by using chloroIluorocarbon blowing agents such as Freon 11 and Freon 12, which can damage the ozone layer. Thus, during the manufacturing of styrofoam, chlorofluorocarbons are usually released into the atmosphere. In addition, when styrofoam is formed using chlorofluorocarbons, certain chlorofluorocarbon blowing agents will leak out 20 of a styrofoam product during the life of the product. Due to these environmental concerns, there has been an increased interest in recent years in finding substitutes for food packaging plastic containers which are degradable and which do not result in the release of harmful substances when being manufactured or burned.
Although paper containers are degradable, a drawback to using paper containers instead of plastic containers for food is that paper absorbs moishlre and grease leading to premature degradation of the container. Thus, in order for paper containers to be adequate substitutes for plastic containers, it is necessary to treat the surface of the paper containers to render them substantially moisture-resistant.
~'C~7~
It is known that paper products and containers can be rendered moisture-lesistant by coating them with various polymers. For example. United States patent No. 3,573,125 discloses that coatings comprised of ethylene-vinyl acetate and wax have been used for years in the packaging field to coat various substrates, including paper. United States patent No. 3,704,157 discloses that paper sheets adapted for packaging can be coated with a copolymer of ethylene and vinyl acetate to impart high moisture barrier properties. United States patent No.
3,298,855 discloses a moisture-resistant wrapping paper prepared by coating paper with blends of polyethylene latex and vinyl acetate copolymer latex. United States patent No. 3,305,383 discloses that the moisture permeability resistance of paper board substrates used to prepare cartons can be enhanced by employing coating compositions containing wax and a copolymer of ethylene and vinyl acetate.
One problem in using polymcr coatings to render paper articles lS moisture resistant is that the polymer coatings serve as a barrier to moisture once the articles are buried in a landfill and thereby inhibit the natural and, at this point, desirable degradation of the paper article. However, once the polymer coating breaks down, the paper article can degrade more readily. Thus, there is a need for a polymer coating which can be applied to paper substrates to render them moistureresistant and which will readily degrade so as to permit the degradation of the substrate.
Various compositions containing cement are disclosed in the prior art.
For example, United States patent No. 3,063,~51 discloses a cement-based paint comprised primarily of Portland cement admixed with a non-aqueous vehicle made up of a small amount of resin dissolved in an ~rganic solven~. The cement-based paint is used to waterproof masonry walls. United States patent No. 2,600,081 discloses a Portland cement-based paint that can be used to coat porous fibre-board material. The Portland cement-based paint contains methyl cellulose.
d ~L
Several patents disclose the use of an ethylene-vinyl acetate copolymer in conjunction with cement. For example, a United States patent No. 4,434,257 discloses a cement composition which is comprised of a mixture of a conventionalcement composition with an ethylene-vinyl acetate copolymer emulsion which contains 5 a polyvinyl alcohol and a fatty acid ester of a polyvalent alcohol. The cement composition can be applied to buildings to improve water resistance.
United States patent No. 4,441,944 discloses a cementitious composition comprising a Portland cement, a polymeric emulsion and flyash. The 10 composition can be foamed and applied to the surface of a sheet~like insulating board which can be made of fibrous cellulose.
United States patent No. 4,395,159 discloses a coating composition applied to a metal substrate to protect the substrate from deterioration. The coating 15 composition comprises a cementitious material, such as Portland cement, a filler, a polymeric material~ such as vinyl acetate polymers and copolymers, and chopped fibres.
United States patent No. 4,844,964 discloses that Portland cement can 20 be mixed with water and an aqueous emulsion of polymers, such as ethylene vinyl acetate copolymers, and then used to prepare a signboard.
The prior art also discloses that variolls acids may be employed to retard the setting time for cement. For example, United States patent No. 4,892,586 25 discloses various organic acids or salts thereof which may be used as retarders for the setting or solidification of cements. Vnited States patent No. 2,470,505 discloses that maleic acid can be added to a cement slurry to act as a retardant to lengthen the stiffening time. United States patent No. 4,054,461 discloses that hydroxypolycarboxylic acid may be used as a retarder in a cement composition, and 30 United States patent No. 3,188,221 discloses that some organic acids may be used as 7 ~
retarding agents for retarding the setting time of eement. Canadian patent No.
638,274 discloses a cement product eontaining Portland eement and ~atty acids.
However, none of the above-mentioned patents discloses a eoating 5 composit;on which can be applied eO a paper substrate to render the substrate moisture resistant during the substrate's useful life but which will readily degrade once the substrate is discarded, sueh as in a landfill, so that the paper substrate can then degrade and disintegrate.
It is an object of the present invention to provide a novel process for preparing a moulded paper stock produet whieh obviates or mitigates a~ least one of the above-mentioned defieienees of the prior art.
Accordingly, the present invention provides a process for preparing a 15 moulded paper product, the process comprising ~he steps of:
(a) providing a pulped paper feedstock;
(b) moulding the pulped paper feedstock to produee a shaped product;
(c) drying the shaped produet;
(d) applying a coating eomposition on to at least one surfaee of the shaped produet; and (e) euring the coating eomposition.
The proeess generally eomprises providing a pulped paper feedstock, 25 moulding the feedstock to produced a shaped product; drying the shaped product;
coating the dried, shaped produet with a eoating eomposition; euring the eoatingcomposition; and, optionally, hot pressing the cured coated produet. Depending on the nature of the coating composition, once the coated produet is discarded in amoisture active landfill, the eoating will begin to break down, thereby allowing the 30 paper substrate to degrade. The eoating composition suitable for use in the present ~ t~
process is not particularly restricted and is preferably degradable to some extent.
Prefereably, the coating composition is comprised of a cement, at least one of a clay and a sulphate and an aqueous emulsion polymer. More preferably, the coating composition further comprises at least one of an organic acid and a wax.
The choice of pulped paper feedstock for use in the present process is not particularly restricted nor is the manner by which it is obtained. Preferably, the pulped paper feedstock is repulped newsprint or other paper-based waste. The following detailed description of an embodiment of the present invention is provided 10 in the context of using a pulped paper feedstock including a repulped newsprint or other paper-based feedstock; however, it will be appreciated that the invention is not limited solely to such a feedstock.
An embodiment of the present invention will be described with 15 reference to the attached Figure in there is illustrated a block diagram of the present process. As shown in the Figure, waste newsprint is repulped, separated, moulded, dried, coated, cured and hot pressed to produce a moulded paper product.
The stock which is used for coating with the composition of the instant 20 invention is preferably a moulded pulp stock which is derived from waste paper, more preferably from waste newsprint and corrugated liner. Of course, virgin pulp andpulp screenings may also be used. In general, the waste paper is received in bullc and manually sorted to remove glossy printed papers which are difflcult to recycle. After sorting, the selected waste paper is transferred by conveyor into a batch repulper, 25 where it is mixed with water, rosin (which is used to size the paper) and an emulsified wax to help reduce moisture abso~ption. Within the batch repulper, the waste paper is beaten into a uniform consistency with a measured quantity of recycled water to produce a pulped paper feedstock having a solids content in the range of about 2 to about 10 percent by weight, preferably from about 3 to about 5 percent by 30 weight.
_5_ J~
In general, the amount of rosin used is in the range of from about 0.5 to about 2 percent by weight, preferably from about 1 to about 3 percent by weight.
The emulsified wax is added in ~he range of from about 0.5 to about 2 percent byweight, preferably from about 1 to about 3 percent by weight. The preferred 5 emulsified waxes are paraffin based, although any waxes which are compatible with the stock solution herein rnay be used. The stock ;s maintained in the batch repulper at a temperature which is normally .slightly above ambient conditions, generally in the range of from about 80F to about 115F, preferably from about 90F to about 100F for about 30 to about 45 minutes or until the fibre is broken down and is in 10 the form of a pulp.
The repulped waste paper stock is then pumped into a raw stock tank where it is held for further processing. From there, the raw stock is pumped into a high density separator to remove debris and other contaminants. Next, the raw stock 15 may or may not be passed over a screen where lumpy material is removed. The lumpy material may then be processed through a refiner and combined with the acceptable material from the screen which together are then pumped to a re~ned stock tank where they are held for further processing at a slightly lower solids content than the raw stock storage.
The reflned material and the material from the high density separator which is not in need of refining are pumped into a tank where they are blended with recirculated water, aluminum sulphate in the range of up to about 1 percent by weight to ;mprove the ability of the rosin to size the paper stock, a defoamer in the range of 25 from about 1 to about 10 parts per million by weight, and other necessary ingredients, depending wpon the end use. Examples of other ingredients include ~llers, additives such as clays, including kaolin, calcium carbonate, as well as polymer de-watering enhancers such as cationic starch. The blended material produced in this step is then suitable for use as pulped paper feedstock in the present process.
lH~VING C~MENT-BASED COATINGS
This invention relates to coating compositions and process for using the 5 coating compositions. More particularly, this invention relates to cemen~-containing coating compositions which can be applied to paper products and the processes for preparing and coating these products.
In recent years, increasing concerns have been expressed about the use 10 of plastic containers~ such as styrofoam cont~iners, in the food industry. Plastic containers, such as those used in grocery stores and fast food restaurants to package food, are not degradable and, as a result, are contributing to the fill-up of landfills.
In addition, when some plastic containers are manufactured or burned, harmful compounds are released into the atmosphere which cause pollution or which damage15 the ozone layer. For example, styrofoam is usually foamed by using chloroIluorocarbon blowing agents such as Freon 11 and Freon 12, which can damage the ozone layer. Thus, during the manufacturing of styrofoam, chlorofluorocarbons are usually released into the atmosphere. In addition, when styrofoam is formed using chlorofluorocarbons, certain chlorofluorocarbon blowing agents will leak out 20 of a styrofoam product during the life of the product. Due to these environmental concerns, there has been an increased interest in recent years in finding substitutes for food packaging plastic containers which are degradable and which do not result in the release of harmful substances when being manufactured or burned.
Although paper containers are degradable, a drawback to using paper containers instead of plastic containers for food is that paper absorbs moishlre and grease leading to premature degradation of the container. Thus, in order for paper containers to be adequate substitutes for plastic containers, it is necessary to treat the surface of the paper containers to render them substantially moisture-resistant.
~'C~7~
It is known that paper products and containers can be rendered moisture-lesistant by coating them with various polymers. For example. United States patent No. 3,573,125 discloses that coatings comprised of ethylene-vinyl acetate and wax have been used for years in the packaging field to coat various substrates, including paper. United States patent No. 3,704,157 discloses that paper sheets adapted for packaging can be coated with a copolymer of ethylene and vinyl acetate to impart high moisture barrier properties. United States patent No.
3,298,855 discloses a moisture-resistant wrapping paper prepared by coating paper with blends of polyethylene latex and vinyl acetate copolymer latex. United States patent No. 3,305,383 discloses that the moisture permeability resistance of paper board substrates used to prepare cartons can be enhanced by employing coating compositions containing wax and a copolymer of ethylene and vinyl acetate.
One problem in using polymcr coatings to render paper articles lS moisture resistant is that the polymer coatings serve as a barrier to moisture once the articles are buried in a landfill and thereby inhibit the natural and, at this point, desirable degradation of the paper article. However, once the polymer coating breaks down, the paper article can degrade more readily. Thus, there is a need for a polymer coating which can be applied to paper substrates to render them moistureresistant and which will readily degrade so as to permit the degradation of the substrate.
Various compositions containing cement are disclosed in the prior art.
For example, United States patent No. 3,063,~51 discloses a cement-based paint comprised primarily of Portland cement admixed with a non-aqueous vehicle made up of a small amount of resin dissolved in an ~rganic solven~. The cement-based paint is used to waterproof masonry walls. United States patent No. 2,600,081 discloses a Portland cement-based paint that can be used to coat porous fibre-board material. The Portland cement-based paint contains methyl cellulose.
d ~L
Several patents disclose the use of an ethylene-vinyl acetate copolymer in conjunction with cement. For example, a United States patent No. 4,434,257 discloses a cement composition which is comprised of a mixture of a conventionalcement composition with an ethylene-vinyl acetate copolymer emulsion which contains 5 a polyvinyl alcohol and a fatty acid ester of a polyvalent alcohol. The cement composition can be applied to buildings to improve water resistance.
United States patent No. 4,441,944 discloses a cementitious composition comprising a Portland cement, a polymeric emulsion and flyash. The 10 composition can be foamed and applied to the surface of a sheet~like insulating board which can be made of fibrous cellulose.
United States patent No. 4,395,159 discloses a coating composition applied to a metal substrate to protect the substrate from deterioration. The coating 15 composition comprises a cementitious material, such as Portland cement, a filler, a polymeric material~ such as vinyl acetate polymers and copolymers, and chopped fibres.
United States patent No. 4,844,964 discloses that Portland cement can 20 be mixed with water and an aqueous emulsion of polymers, such as ethylene vinyl acetate copolymers, and then used to prepare a signboard.
The prior art also discloses that variolls acids may be employed to retard the setting time for cement. For example, United States patent No. 4,892,586 25 discloses various organic acids or salts thereof which may be used as retarders for the setting or solidification of cements. Vnited States patent No. 2,470,505 discloses that maleic acid can be added to a cement slurry to act as a retardant to lengthen the stiffening time. United States patent No. 4,054,461 discloses that hydroxypolycarboxylic acid may be used as a retarder in a cement composition, and 30 United States patent No. 3,188,221 discloses that some organic acids may be used as 7 ~
retarding agents for retarding the setting time of eement. Canadian patent No.
638,274 discloses a cement product eontaining Portland eement and ~atty acids.
However, none of the above-mentioned patents discloses a eoating 5 composit;on which can be applied eO a paper substrate to render the substrate moisture resistant during the substrate's useful life but which will readily degrade once the substrate is discarded, sueh as in a landfill, so that the paper substrate can then degrade and disintegrate.
It is an object of the present invention to provide a novel process for preparing a moulded paper stock produet whieh obviates or mitigates a~ least one of the above-mentioned defieienees of the prior art.
Accordingly, the present invention provides a process for preparing a 15 moulded paper product, the process comprising ~he steps of:
(a) providing a pulped paper feedstock;
(b) moulding the pulped paper feedstock to produee a shaped product;
(c) drying the shaped produet;
(d) applying a coating eomposition on to at least one surfaee of the shaped produet; and (e) euring the coating eomposition.
The proeess generally eomprises providing a pulped paper feedstock, 25 moulding the feedstock to produced a shaped product; drying the shaped product;
coating the dried, shaped produet with a eoating eomposition; euring the eoatingcomposition; and, optionally, hot pressing the cured coated produet. Depending on the nature of the coating composition, once the coated produet is discarded in amoisture active landfill, the eoating will begin to break down, thereby allowing the 30 paper substrate to degrade. The eoating composition suitable for use in the present ~ t~
process is not particularly restricted and is preferably degradable to some extent.
Prefereably, the coating composition is comprised of a cement, at least one of a clay and a sulphate and an aqueous emulsion polymer. More preferably, the coating composition further comprises at least one of an organic acid and a wax.
The choice of pulped paper feedstock for use in the present process is not particularly restricted nor is the manner by which it is obtained. Preferably, the pulped paper feedstock is repulped newsprint or other paper-based waste. The following detailed description of an embodiment of the present invention is provided 10 in the context of using a pulped paper feedstock including a repulped newsprint or other paper-based feedstock; however, it will be appreciated that the invention is not limited solely to such a feedstock.
An embodiment of the present invention will be described with 15 reference to the attached Figure in there is illustrated a block diagram of the present process. As shown in the Figure, waste newsprint is repulped, separated, moulded, dried, coated, cured and hot pressed to produce a moulded paper product.
The stock which is used for coating with the composition of the instant 20 invention is preferably a moulded pulp stock which is derived from waste paper, more preferably from waste newsprint and corrugated liner. Of course, virgin pulp andpulp screenings may also be used. In general, the waste paper is received in bullc and manually sorted to remove glossy printed papers which are difflcult to recycle. After sorting, the selected waste paper is transferred by conveyor into a batch repulper, 25 where it is mixed with water, rosin (which is used to size the paper) and an emulsified wax to help reduce moisture abso~ption. Within the batch repulper, the waste paper is beaten into a uniform consistency with a measured quantity of recycled water to produce a pulped paper feedstock having a solids content in the range of about 2 to about 10 percent by weight, preferably from about 3 to about 5 percent by 30 weight.
_5_ J~
In general, the amount of rosin used is in the range of from about 0.5 to about 2 percent by weight, preferably from about 1 to about 3 percent by weight.
The emulsified wax is added in ~he range of from about 0.5 to about 2 percent byweight, preferably from about 1 to about 3 percent by weight. The preferred 5 emulsified waxes are paraffin based, although any waxes which are compatible with the stock solution herein rnay be used. The stock ;s maintained in the batch repulper at a temperature which is normally .slightly above ambient conditions, generally in the range of from about 80F to about 115F, preferably from about 90F to about 100F for about 30 to about 45 minutes or until the fibre is broken down and is in 10 the form of a pulp.
The repulped waste paper stock is then pumped into a raw stock tank where it is held for further processing. From there, the raw stock is pumped into a high density separator to remove debris and other contaminants. Next, the raw stock 15 may or may not be passed over a screen where lumpy material is removed. The lumpy material may then be processed through a refiner and combined with the acceptable material from the screen which together are then pumped to a re~ned stock tank where they are held for further processing at a slightly lower solids content than the raw stock storage.
The reflned material and the material from the high density separator which is not in need of refining are pumped into a tank where they are blended with recirculated water, aluminum sulphate in the range of up to about 1 percent by weight to ;mprove the ability of the rosin to size the paper stock, a defoamer in the range of 25 from about 1 to about 10 parts per million by weight, and other necessary ingredients, depending wpon the end use. Examples of other ingredients include ~llers, additives such as clays, including kaolin, calcium carbonate, as well as polymer de-watering enhancers such as cationic starch. The blended material produced in this step is then suitable for use as pulped paper feedstock in the present process.
2~ 7~
The blended material, in this instance the pulped paper feedstock for the present process, is then transferred to the moulding vat where additional water is added to reduce the solids content to from about 0.3 to about 2.0 percent by weight, preferably from about 0.5 to about 1.0 percent by weight. In the moulding vat, the 5 pulp stock is con.inuously recirculated as it is exposed to the vacuum moulder which is designed to form the product to be utilized. In general, particularly with small items such as food trays, the moulder will form large size assemblies containingmultiple units of the item to be ~ormed. For example, with food trays the overall size of the assembly is about 14 x 25 inches and contains about 3-9 food trays per 10 assembly. The moulding machine itself comprises, in addition to the moulding vat, the vacuum moulder and the transfer dye mechanism. The vacuum moulder consists of a moulding drum, preferably having several faces cont uning dyes having the shape of the desired product. As the drum rotates, each face in succession is dipped into the pulp stock. A vacuum system attached to the rotating drum causes the fibres 15 contained in the pump stock to be deposited onto the forming dyes on the face of the drum as the water in which the fibres are suspended is drawn through the dyes and drained out. DuAng the moulding operation the fibres orAent in a mechanically-interlocked layer to form the moulded product. The removed water is recycled forfurther use. As the moulding drum continues to rotate, at a point just prior to re-20 entry into the vat, a rotating transfer dye mates vvith the moulded face on the drumand, under suction, removes the wet moulded product, depositing it on a conveyor line. Moulders of the type which may be used in the present process are further descAbed in United States patent No. 3,661,707.
The wet moulded product is then transferred into a dryer where it is dAed for a peAod of time and under temperature conditions which are adjusted depending upon the size, shape and end use of the particular product being moulded.
In general, for paper trays, the product is dAed at an oven temperature in the range of from about 375F to about 500P, preferably from about 400F to about 450F, for period of time in the range of from about 10 to about 30 minutes. Preferably, as ~ ~'7~
the product leaves the dryer, it will have achieved a surface temperature of from a~out 180F to about 230F.
After exiting the dryer, the product may be coated with a coating 5 composition usin~ one of several coating application ~echniques as described above.
However, the preferred method involves spray coating. In order to minimize moisture and coating absorption, the tray assembly is reheated immediately before coating in an oven at the same temperature described above so that the ~emperature of the assembly is again elevated to a value in the range of from about 190F to10 about 230F. After one side of the tray assembly is coated, the assembly is then reheated to about 190F and the second side is coated. Preferably, the back or rough side of the tray assembly will be coated to a 3 mil dry film thickness while the front or smooth side will be coated to about a 1.5 mil dry film thickness. While the coating processes which are employed, as pointed out above, may vary, it is preferred 15 to use a two-step spraying process employing an air-assisted, low pressure spray followed by an electrostatic spraying.
As described above, in addition, different coatings may be applied to the front and to the back of the article and multiple coatings may be applied, 20 depending upon the particular end use.
After the assembly is coated, it is preferably passed through a 350F
to 500F curing oven where it is maintained for a period of from about 30 seconds to several minutes, all again depending upon the coating composition and the desired 25 end use involved.
After curing, the assembly may then be hot-pressed using a standard press for a period of from about 0.2 to about 2 seconds, at temperatures rangingbetween about 250F and about 400F, and at a pressure of from about 50 ~o about30 25Q psi. The purpose of hot-pressing is to smooth the coating and to add gloss.
2~ 7~
After the coated assembly leaves the hot press it is then, in the preferred instance, disassembled by cutting, stacked and stored for shipment.
The prefierred coating composition suitable for use in tlle present 5 process compr~ses a cement, more preferably white Portland cement.
The preferred coating composition also preferably comprises a clay.
The clay should be of extremely fine particle size and should consist of one or more clay minerals, including hydrosilicates of aluminum, iron or magnesium. Most 10 preferred among the clays are the kaolin clays which include kaolin;te dickite and halloysite-endellite. Clays are well known in the art and the appropriate c]ay for use in the preferred coating composition would be apparent to a person skilled in the art.
In addition to the clay, another component of the preferred coating 15 composition for use in the present process is a sulphate, preferably, an alkali or alkaline earth metal sulphate, and most preferably, calcium sulphate.
The cement, clay and sulphate suitable for use in the preferred coating composition are readily available commercially.
The preferred coating composition also contains an aqueous emulsion polymer which, preferably, has F:DA (or other appropriate governmental) approval, if the finished product is to be used in a food-type application. Any aqueous emulsion polymer which will impart water resistance to a paper substrate may be 25 employed as long as it will not be degraded or otherwise break down at a relatively high pH or in the presence of a cement. Preferably, the polymer is a carboxyl functional emulsion polymer, such as acrylic, polyester, epoxy, vinyl, vinyl acetate, ethylene-vinyl acetate, or epoxy ester polymer or copolymer. Most preferably, the emulsion polymer is an ethylene-vinyl acetate aqueous emulsion copolymer.
The blended material, in this instance the pulped paper feedstock for the present process, is then transferred to the moulding vat where additional water is added to reduce the solids content to from about 0.3 to about 2.0 percent by weight, preferably from about 0.5 to about 1.0 percent by weight. In the moulding vat, the 5 pulp stock is con.inuously recirculated as it is exposed to the vacuum moulder which is designed to form the product to be utilized. In general, particularly with small items such as food trays, the moulder will form large size assemblies containingmultiple units of the item to be ~ormed. For example, with food trays the overall size of the assembly is about 14 x 25 inches and contains about 3-9 food trays per 10 assembly. The moulding machine itself comprises, in addition to the moulding vat, the vacuum moulder and the transfer dye mechanism. The vacuum moulder consists of a moulding drum, preferably having several faces cont uning dyes having the shape of the desired product. As the drum rotates, each face in succession is dipped into the pulp stock. A vacuum system attached to the rotating drum causes the fibres 15 contained in the pump stock to be deposited onto the forming dyes on the face of the drum as the water in which the fibres are suspended is drawn through the dyes and drained out. DuAng the moulding operation the fibres orAent in a mechanically-interlocked layer to form the moulded product. The removed water is recycled forfurther use. As the moulding drum continues to rotate, at a point just prior to re-20 entry into the vat, a rotating transfer dye mates vvith the moulded face on the drumand, under suction, removes the wet moulded product, depositing it on a conveyor line. Moulders of the type which may be used in the present process are further descAbed in United States patent No. 3,661,707.
The wet moulded product is then transferred into a dryer where it is dAed for a peAod of time and under temperature conditions which are adjusted depending upon the size, shape and end use of the particular product being moulded.
In general, for paper trays, the product is dAed at an oven temperature in the range of from about 375F to about 500P, preferably from about 400F to about 450F, for period of time in the range of from about 10 to about 30 minutes. Preferably, as ~ ~'7~
the product leaves the dryer, it will have achieved a surface temperature of from a~out 180F to about 230F.
After exiting the dryer, the product may be coated with a coating 5 composition usin~ one of several coating application ~echniques as described above.
However, the preferred method involves spray coating. In order to minimize moisture and coating absorption, the tray assembly is reheated immediately before coating in an oven at the same temperature described above so that the ~emperature of the assembly is again elevated to a value in the range of from about 190F to10 about 230F. After one side of the tray assembly is coated, the assembly is then reheated to about 190F and the second side is coated. Preferably, the back or rough side of the tray assembly will be coated to a 3 mil dry film thickness while the front or smooth side will be coated to about a 1.5 mil dry film thickness. While the coating processes which are employed, as pointed out above, may vary, it is preferred 15 to use a two-step spraying process employing an air-assisted, low pressure spray followed by an electrostatic spraying.
As described above, in addition, different coatings may be applied to the front and to the back of the article and multiple coatings may be applied, 20 depending upon the particular end use.
After the assembly is coated, it is preferably passed through a 350F
to 500F curing oven where it is maintained for a period of from about 30 seconds to several minutes, all again depending upon the coating composition and the desired 25 end use involved.
After curing, the assembly may then be hot-pressed using a standard press for a period of from about 0.2 to about 2 seconds, at temperatures rangingbetween about 250F and about 400F, and at a pressure of from about 50 ~o about30 25Q psi. The purpose of hot-pressing is to smooth the coating and to add gloss.
2~ 7~
After the coated assembly leaves the hot press it is then, in the preferred instance, disassembled by cutting, stacked and stored for shipment.
The prefierred coating composition suitable for use in tlle present 5 process compr~ses a cement, more preferably white Portland cement.
The preferred coating composition also preferably comprises a clay.
The clay should be of extremely fine particle size and should consist of one or more clay minerals, including hydrosilicates of aluminum, iron or magnesium. Most 10 preferred among the clays are the kaolin clays which include kaolin;te dickite and halloysite-endellite. Clays are well known in the art and the appropriate c]ay for use in the preferred coating composition would be apparent to a person skilled in the art.
In addition to the clay, another component of the preferred coating 15 composition for use in the present process is a sulphate, preferably, an alkali or alkaline earth metal sulphate, and most preferably, calcium sulphate.
The cement, clay and sulphate suitable for use in the preferred coating composition are readily available commercially.
The preferred coating composition also contains an aqueous emulsion polymer which, preferably, has F:DA (or other appropriate governmental) approval, if the finished product is to be used in a food-type application. Any aqueous emulsion polymer which will impart water resistance to a paper substrate may be 25 employed as long as it will not be degraded or otherwise break down at a relatively high pH or in the presence of a cement. Preferably, the polymer is a carboxyl functional emulsion polymer, such as acrylic, polyester, epoxy, vinyl, vinyl acetate, ethylene-vinyl acetate, or epoxy ester polymer or copolymer. Most preferably, the emulsion polymer is an ethylene-vinyl acetate aqueous emulsion copolymer.
3~
The ethylene-vinyl acetate copolymers which are suitable can be prepared by copolymerizing a mixture of ethylene and vinyl acetate in the presence of a free-radical catalyst. Suitable ethylene-vinyl acetate emulsion compositions are readily available commercially. One example of a suitable emulsion copolymer is 5 Air~exTM 100 HS latex, available from Air Produces and Chemicals, Inc.
The preferred coating composition for use in the present process more preferably further comprises a wax, most preferably a wax emulsion, to aid in press release and to retard water and o~her moisture absorption. The waxes which may be 10 used herein may either be synthetic or naturally occurring. However, in order for the wax to carry out its intended function, it is important that the wax not degrade in the presence of other components in the coating composition. Among the waxes which may be used are included naturally occurring waxes such as esters of long chain fatty alcohols and acids, petroleum and`rnineral waxes. Among the common 15 waxes which rnay be used are the vegetable waxes such as carnauba wax, candelilla wax, and hydrogenated candelilla wax. Other waxes include the synthetic waxes such as polyethylene waxes and paraffin waxes, these latter waxes being preferred.
The preferred coating composition more preferably further comprises 20 an organic acid, such as maleic, stearic, potassium hydrogen t~rtrate or oleic acid or any organic sugar such as corn syrup, which serves to retard the setting time of the coating compositions. Difunctional acids are preferred. The presence of an organic acid in the coating composition helps to prolong the pot life and to make it easier to spray the composition onto a degradable substrate such as a paper substrate.
In addition to the above-described components, the coating composition may contain conventional fillers, additives, thickeners, defoamers and pigments.Since the cement coating composition can be readily applied to paper substrates, such as vacuum moulded pulp food trays, and since pigments can be readily added to the 2~ '~'7'1~
coating composition, the coating composition provides a relatively easy means for colouring the surface of a paper substrate a particular colour.
Preferably, the coating composition is prepared by first combining the 5 clay, the sulphate, the acid and the aqueous emulsion polymer in water. The cement should be added shortly before the coating composition is applied to a paper substrate because the coating composition has a pot life of up to 24 hours once the cement is added.
Generally, the preferred coating composition will contain from about 40 to about 90 percent by weight cement, preferably from about 50 to about 75 percent by weight; from 0 to about 20 percent by weight of a clay, preferably from about 2 to about 10 percent by weight; from 0 to about 20 percent by weight of sulphate, preferably from about 1 to about 15 percent by weight; and from about 6 15 to about 60 percent by solids weight of the aqueous emulsion polymer, preferably from about 10 to about 40 percent by weight; with the plOViSO that at least one of the clay and the sulphate are actually present in the composition. All weights are based upon the total solids weight of aqueous emulsion polymer, cement, sulphate, and clay in the coating composition.
In the event an organic acid or sugar is added, it should be added in an amount in the range of from about 1 to about 20 percent based on the above compositional weight. In the event a wax is added, it should be added in an amount in the range of from about the 1 to about 25 percent by weight solids level based on 25 the above compositional weight.
In order for the paper substrate to disintegrate after it is discarded, it is necessary for the coating composition to break down and degrade so that the paper substrate can degrade. The intact cement coating serves as a protective coating ~or 30 the paper substrate thereby inhibiting premature disintegration of the paper substrate.
7~
Once the cement coating begins to break down and degrade, the paper substrate can also begin to degrade.
Dis;ntegration of the coating composition, and thus of the paper S substrate, will occur when the degradable coating is placed on at least one side of the paper substrate. Faster disintegration, of course, will occur when both sides of the paper substrate are coated with the degradable coating. However, it is possible to coat one side with the degradable coating described herein and another side with a more conventional coating or a less degradable coating. In general, with food 10 products a less degradable or non-degradable coating is placed on the side of the paper which will be exposed to the food product and the reverse side is coated with the composition described herein. The partially degradable compositions which may be used in conjunction with the coating compositions described otherwise herein simply involve the use of higher percentages of the coating composition of the 15 emulsions described herein and lesser amounts of the cement and other components.
When the cement and other components are totally removed, of course, the coatingcomposition becomes essentially non-degradable.
A particularly preferred coating composition which still maintains 20 certain degradative properties but which exhibits heightened resistance to liquids, generally, and food liquid specifically, involves a coating composition comprising:
from about 15 to about 60 percent by weight of a cement; from about 40 to about 75 percent by weight on a solids basis of aqueo-ls emulsion polymer; from 0 to about 20 percent, preferably from about 1 to 20 percent of sulphate; and from 0 to about 10 25 percent, preferably from about 1 to 10 percent of a clay, all as described above.
The coating composition used in the present process may be applied by conventional spraying or a;rless sprayin~, with or without electrostatic assist. In addition, electrostatic discs may be used to apply the coating compositions during the 30 present process.
Although not wishing to be limited to any particular theory or mode of the degradation the cement in the preferred coating composition, it is believed that the sulphate (e.g. calcium sulphate) in the preferred coating absorbs water and forms a complex with the kaolin which causes the cement to form a slush and the dried 5 coating to break down. As a result of the presence of the sulphate, kaolin and cement in the preferred coating, the coating will readily degrade and decompose within a few years in a moisture, and preferably biologically, active environment such as a landfill, there~y allowing the paper substrate also to degrade.
10Since the preferred coating composition for use in the present process is substantially non-toxic, it may be used to coat paper articles for food storage, such as vacuum moulded paper food trays used in the fast food industry. The paper containers coated with the coating composition have a semi-lustrous finish and smooth surface texture and are resistant to food juices`and moisture.
Embodiments of the present invention will be described with reference to the following Examples which are provided for illustrative purposes only and should not be used to limit the scope of the in~ention. In the following Examples, all parts are by weight, unless otherwise specified.
Example 1 Components A and B were prepared as follows:
25Component A
24.39 parts water were blended under agitation with 0.41 parts of a NatrosolTM 330 thickener available from Aqualon Co., 0.96 parts of TamolTM 850 surfactant available from Rohm & Haas Co., 0.30 parts of ammonium hydroxide and 0.54 parts of DrewplusTM L140 defoamer available from Drew Chemical. Also added 30with agitation were 16.8 parts of KronosTM 2020 titanium dioxide available from Kronos, Inc., 2.57 parts of ~itoxTM titanium dioxide available from Hitox Corporation of America, along with ~.57 parts of burnt umber pigment and 14.98 parts of calcium carbonate. 20.74 parts of water, 127.99 parts of Air~ex 100, anEVA emulsion (aqueous emulsion polymer) available from Air Products & Chemicals Company and 90.17 parts of MichemlubTM 368, a wax emuls;on available from Michelman Chemical Co were then added to the mixture.
Component B
17.95 parts of water were blended with 7.11 parts of corn syrup, 3.66 10 parts of ammonium hydroxide, 9.33 parts of potassium hydrogen tartrate, 9.33 parts of TamolTM 850, 24.70 parts of HuberTM 35, a kaolin clay (clay), 9.89 parts of calcium sulphate (sulphate), and 1.08 parts of DrewplusTM L140. To this mixture was added a total 156.88 parts of tap water, and 459.8~ parts of white Portland cement type I (cement).
1~
Components A and B were then mixed together and exhibited a pot life of two hours. Over this period of time the mixture could readily be applied to reconstituted paper or cardboard ~ats by spraying as well as by other conventional coating means.
A coating of the Component A and Component B mixture was sprayed to a thickness of 3 mils on reconstituted paper plates using, in one case, a standard spray gun and, in another case, an electrostatic disc. The plates were dried in a 350F oven. The plates were then placed in a platen press and heated at a 25 temperature of 100 C and under 100 psi for about 1 second. A uniform, smoothcoating resulted. The coatings degraded when p]aced in a mo;sture active landfill, i.e., a landfill containing sufficient moisture to degrade the coating in question over time.
7~t7~
Example 2 A two-component coating composition was prepared as follows:
S Component A
69.12 parts of water were mixed with 1.50 parts of NatrosolTM 330, 2.73 parts of TamolTM 850, 0.30 parts of ammonium hydroxide, 1.54 parts of DrewplusTM L140 defoamer. Added to this mixture under agitation were 47.62 partsof KronosTM 2020, 7.30 parts of HitoxTM titanium dioxide, 0.96 parts of burnt umber pigment, 42.46 parts of calcium carbonate, 58.77 parts of water, 362.70 parts ofAir~exTM 100 emulsion, and 255.54 parts of wax emulsion.
Component B
3.58 parts of water were mixed with 1.52 parts of corn syrup, 0.79 parts of ammonium hydroxide, 2.0 parts of potassium hydrogen tartrate, 2.0 parts of TamolTM 850, 5.30 parts of HuberTM 35 clay, 2.13 parts of calcium sulphate, and 0.23 parts of DrewplusTM L140. Added for viscosity control were 33.65 parts of water. Finally 98.64 parts of white Portland cement type I were added to the mixture.
Components A and B were blended and sprayed to a thickness of 5 mil on a reconstituted paper plate stock, dried and cured as in Example 1. The reverse side of the plate was sprayed, dried and cured with the blend described in Example 1.
The coated plates were then brought in contact with meat products.
The inside coating using the Example 2 composition showed excellent resistance to the meat product. When the coated plate is exposed to a moisture active landfill, it degraded.
As can be seen, the Example 2 blend contains a much higher level of emulsion than does Example 1 so as to retard food liquid penekation of the cardboard stock. On the other hand, the mateAal prepared ;n Example 1 is much more readilydegradable because of its high concentration of cement and its relatively low amount 5 of emulsion polymer.
The ethylene-vinyl acetate copolymers which are suitable can be prepared by copolymerizing a mixture of ethylene and vinyl acetate in the presence of a free-radical catalyst. Suitable ethylene-vinyl acetate emulsion compositions are readily available commercially. One example of a suitable emulsion copolymer is 5 Air~exTM 100 HS latex, available from Air Produces and Chemicals, Inc.
The preferred coating composition for use in the present process more preferably further comprises a wax, most preferably a wax emulsion, to aid in press release and to retard water and o~her moisture absorption. The waxes which may be 10 used herein may either be synthetic or naturally occurring. However, in order for the wax to carry out its intended function, it is important that the wax not degrade in the presence of other components in the coating composition. Among the waxes which may be used are included naturally occurring waxes such as esters of long chain fatty alcohols and acids, petroleum and`rnineral waxes. Among the common 15 waxes which rnay be used are the vegetable waxes such as carnauba wax, candelilla wax, and hydrogenated candelilla wax. Other waxes include the synthetic waxes such as polyethylene waxes and paraffin waxes, these latter waxes being preferred.
The preferred coating composition more preferably further comprises 20 an organic acid, such as maleic, stearic, potassium hydrogen t~rtrate or oleic acid or any organic sugar such as corn syrup, which serves to retard the setting time of the coating compositions. Difunctional acids are preferred. The presence of an organic acid in the coating composition helps to prolong the pot life and to make it easier to spray the composition onto a degradable substrate such as a paper substrate.
In addition to the above-described components, the coating composition may contain conventional fillers, additives, thickeners, defoamers and pigments.Since the cement coating composition can be readily applied to paper substrates, such as vacuum moulded pulp food trays, and since pigments can be readily added to the 2~ '~'7'1~
coating composition, the coating composition provides a relatively easy means for colouring the surface of a paper substrate a particular colour.
Preferably, the coating composition is prepared by first combining the 5 clay, the sulphate, the acid and the aqueous emulsion polymer in water. The cement should be added shortly before the coating composition is applied to a paper substrate because the coating composition has a pot life of up to 24 hours once the cement is added.
Generally, the preferred coating composition will contain from about 40 to about 90 percent by weight cement, preferably from about 50 to about 75 percent by weight; from 0 to about 20 percent by weight of a clay, preferably from about 2 to about 10 percent by weight; from 0 to about 20 percent by weight of sulphate, preferably from about 1 to about 15 percent by weight; and from about 6 15 to about 60 percent by solids weight of the aqueous emulsion polymer, preferably from about 10 to about 40 percent by weight; with the plOViSO that at least one of the clay and the sulphate are actually present in the composition. All weights are based upon the total solids weight of aqueous emulsion polymer, cement, sulphate, and clay in the coating composition.
In the event an organic acid or sugar is added, it should be added in an amount in the range of from about 1 to about 20 percent based on the above compositional weight. In the event a wax is added, it should be added in an amount in the range of from about the 1 to about 25 percent by weight solids level based on 25 the above compositional weight.
In order for the paper substrate to disintegrate after it is discarded, it is necessary for the coating composition to break down and degrade so that the paper substrate can degrade. The intact cement coating serves as a protective coating ~or 30 the paper substrate thereby inhibiting premature disintegration of the paper substrate.
7~
Once the cement coating begins to break down and degrade, the paper substrate can also begin to degrade.
Dis;ntegration of the coating composition, and thus of the paper S substrate, will occur when the degradable coating is placed on at least one side of the paper substrate. Faster disintegration, of course, will occur when both sides of the paper substrate are coated with the degradable coating. However, it is possible to coat one side with the degradable coating described herein and another side with a more conventional coating or a less degradable coating. In general, with food 10 products a less degradable or non-degradable coating is placed on the side of the paper which will be exposed to the food product and the reverse side is coated with the composition described herein. The partially degradable compositions which may be used in conjunction with the coating compositions described otherwise herein simply involve the use of higher percentages of the coating composition of the 15 emulsions described herein and lesser amounts of the cement and other components.
When the cement and other components are totally removed, of course, the coatingcomposition becomes essentially non-degradable.
A particularly preferred coating composition which still maintains 20 certain degradative properties but which exhibits heightened resistance to liquids, generally, and food liquid specifically, involves a coating composition comprising:
from about 15 to about 60 percent by weight of a cement; from about 40 to about 75 percent by weight on a solids basis of aqueo-ls emulsion polymer; from 0 to about 20 percent, preferably from about 1 to 20 percent of sulphate; and from 0 to about 10 25 percent, preferably from about 1 to 10 percent of a clay, all as described above.
The coating composition used in the present process may be applied by conventional spraying or a;rless sprayin~, with or without electrostatic assist. In addition, electrostatic discs may be used to apply the coating compositions during the 30 present process.
Although not wishing to be limited to any particular theory or mode of the degradation the cement in the preferred coating composition, it is believed that the sulphate (e.g. calcium sulphate) in the preferred coating absorbs water and forms a complex with the kaolin which causes the cement to form a slush and the dried 5 coating to break down. As a result of the presence of the sulphate, kaolin and cement in the preferred coating, the coating will readily degrade and decompose within a few years in a moisture, and preferably biologically, active environment such as a landfill, there~y allowing the paper substrate also to degrade.
10Since the preferred coating composition for use in the present process is substantially non-toxic, it may be used to coat paper articles for food storage, such as vacuum moulded paper food trays used in the fast food industry. The paper containers coated with the coating composition have a semi-lustrous finish and smooth surface texture and are resistant to food juices`and moisture.
Embodiments of the present invention will be described with reference to the following Examples which are provided for illustrative purposes only and should not be used to limit the scope of the in~ention. In the following Examples, all parts are by weight, unless otherwise specified.
Example 1 Components A and B were prepared as follows:
25Component A
24.39 parts water were blended under agitation with 0.41 parts of a NatrosolTM 330 thickener available from Aqualon Co., 0.96 parts of TamolTM 850 surfactant available from Rohm & Haas Co., 0.30 parts of ammonium hydroxide and 0.54 parts of DrewplusTM L140 defoamer available from Drew Chemical. Also added 30with agitation were 16.8 parts of KronosTM 2020 titanium dioxide available from Kronos, Inc., 2.57 parts of ~itoxTM titanium dioxide available from Hitox Corporation of America, along with ~.57 parts of burnt umber pigment and 14.98 parts of calcium carbonate. 20.74 parts of water, 127.99 parts of Air~ex 100, anEVA emulsion (aqueous emulsion polymer) available from Air Products & Chemicals Company and 90.17 parts of MichemlubTM 368, a wax emuls;on available from Michelman Chemical Co were then added to the mixture.
Component B
17.95 parts of water were blended with 7.11 parts of corn syrup, 3.66 10 parts of ammonium hydroxide, 9.33 parts of potassium hydrogen tartrate, 9.33 parts of TamolTM 850, 24.70 parts of HuberTM 35, a kaolin clay (clay), 9.89 parts of calcium sulphate (sulphate), and 1.08 parts of DrewplusTM L140. To this mixture was added a total 156.88 parts of tap water, and 459.8~ parts of white Portland cement type I (cement).
1~
Components A and B were then mixed together and exhibited a pot life of two hours. Over this period of time the mixture could readily be applied to reconstituted paper or cardboard ~ats by spraying as well as by other conventional coating means.
A coating of the Component A and Component B mixture was sprayed to a thickness of 3 mils on reconstituted paper plates using, in one case, a standard spray gun and, in another case, an electrostatic disc. The plates were dried in a 350F oven. The plates were then placed in a platen press and heated at a 25 temperature of 100 C and under 100 psi for about 1 second. A uniform, smoothcoating resulted. The coatings degraded when p]aced in a mo;sture active landfill, i.e., a landfill containing sufficient moisture to degrade the coating in question over time.
7~t7~
Example 2 A two-component coating composition was prepared as follows:
S Component A
69.12 parts of water were mixed with 1.50 parts of NatrosolTM 330, 2.73 parts of TamolTM 850, 0.30 parts of ammonium hydroxide, 1.54 parts of DrewplusTM L140 defoamer. Added to this mixture under agitation were 47.62 partsof KronosTM 2020, 7.30 parts of HitoxTM titanium dioxide, 0.96 parts of burnt umber pigment, 42.46 parts of calcium carbonate, 58.77 parts of water, 362.70 parts ofAir~exTM 100 emulsion, and 255.54 parts of wax emulsion.
Component B
3.58 parts of water were mixed with 1.52 parts of corn syrup, 0.79 parts of ammonium hydroxide, 2.0 parts of potassium hydrogen tartrate, 2.0 parts of TamolTM 850, 5.30 parts of HuberTM 35 clay, 2.13 parts of calcium sulphate, and 0.23 parts of DrewplusTM L140. Added for viscosity control were 33.65 parts of water. Finally 98.64 parts of white Portland cement type I were added to the mixture.
Components A and B were blended and sprayed to a thickness of 5 mil on a reconstituted paper plate stock, dried and cured as in Example 1. The reverse side of the plate was sprayed, dried and cured with the blend described in Example 1.
The coated plates were then brought in contact with meat products.
The inside coating using the Example 2 composition showed excellent resistance to the meat product. When the coated plate is exposed to a moisture active landfill, it degraded.
As can be seen, the Example 2 blend contains a much higher level of emulsion than does Example 1 so as to retard food liquid penekation of the cardboard stock. On the other hand, the mateAal prepared ;n Example 1 is much more readilydegradable because of its high concentration of cement and its relatively low amount 5 of emulsion polymer.
Claims (13)
1. A process for preparing a moulded paper product, the process comprising the steps of:
(a) providing a pulped paper feedstock;
(b) moulding the pulped paper feedstock to produce a shaped product;
(c) drying the shaped product;
(d) applying a coating composition on to at least one surface of the shaped product; and (e) curing the coating composition.
(a) providing a pulped paper feedstock;
(b) moulding the pulped paper feedstock to produce a shaped product;
(c) drying the shaped product;
(d) applying a coating composition on to at least one surface of the shaped product; and (e) curing the coating composition.
2. The process defined in claim 1, wherein the pulped paper feedstock is substantially free of any undesirable materials.
3. The process defined in claim 1, further comprising the step of:
(f) hot pressing the coating composition after curing to produce a hot pressed product.
(f) hot pressing the coating composition after curing to produce a hot pressed product.
4. The process defined in claim 3, further comprising the step of:
(g) cutting and trimming the hot pressed product.
(g) cutting and trimming the hot pressed product.
5. The process defined in claim 1, wherein step (b) comprises moulding the pulped paper feedstock on a vacuum moulder.
6. The process defined in claim 1, wherein step (c) comprises drying the shaped product at a temperature in the range of from about 375°F to about 500°F and step (e) comprises curing the coating composition at a temperature in the range of from about 350°F to about 500°F.
7. The process defined in claim 3, wherein step (f) the hot pressing comprises hot pressing the coating composition at elevated temperature.
8. The process defined in claim 1, wherein the moulded product is a product for use with food.
9. The process defined in claim 1, wherein the pulped paper feedstock comprises waste paper.
10. The process defined in claim 1, wherein the coating coating composition comprises:
(a) a cement;
(b) at least one of a clay and a sulphate; and (c) an aqueous emulsion polymer which is substantially stable in the presence of the other components in said coating composition.
(a) a cement;
(b) at least one of a clay and a sulphate; and (c) an aqueous emulsion polymer which is substantially stable in the presence of the other components in said coating composition.
11. The process defined in claim 10, wherein both of the clay and the sulphate are present.
12. The process defined in claim 10, wherein the coating composition further comprises at least one of a wax, an organic acid and a sugar.
13. The process defined in claim 1, wherein the coating composition:
(a) from about 40 to about 90 percent by weight of said cement;
(b) from 0 to about 20 percent by weight of said clay;
(c) from about 0 to about 20 percent by weight of said sulphate; and (d) from about 6 to about 60 percent by weight of said emulsion polymer;
all based on the total weight of said cement, said clay, said sulphate and the solids weight of said emulsion polymer.
(a) from about 40 to about 90 percent by weight of said cement;
(b) from 0 to about 20 percent by weight of said clay;
(c) from about 0 to about 20 percent by weight of said sulphate; and (d) from about 6 to about 60 percent by weight of said emulsion polymer;
all based on the total weight of said cement, said clay, said sulphate and the solids weight of said emulsion polymer.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US74803191A | 1991-08-21 | 1991-08-21 | |
US07/748,031 | 1991-08-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2057474A1 true CA2057474A1 (en) | 1993-02-22 |
Family
ID=25007686
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002057474A Abandoned CA2057474A1 (en) | 1991-08-21 | 1991-12-10 | Process for forming paper-based products having cement-based coatings |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0532445A1 (en) |
CA (1) | CA2057474A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6245388B1 (en) | 1999-06-30 | 2001-06-12 | The Chinet Company Technology | Wave coating of articles |
CN109629283A (en) * | 2018-12-05 | 2019-04-16 | 广东轻工职业技术学院 | A kind of paper idiosome and the preparation method and application thereof |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6250985B1 (en) * | 1998-02-02 | 2001-06-26 | Joseph A. Nicholson | Hollow breakable object having a breakable dye absorptive coating |
US7396438B2 (en) | 2003-09-22 | 2008-07-08 | Tembec Industries Inc. | Lignocellulose fiber-resin composite material |
DE102019127560A1 (en) * | 2019-10-14 | 2021-04-15 | Kiefel Gmbh | FIBER MOLDING LINE FOR THE PRODUCTION OF MOLDED PARTS FROM ENVIRONMENTALLY COMPATIBLE DEGRADABLE FIBER MATERIAL |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2236900A (en) * | 1935-09-06 | 1941-04-01 | Carey Philip Mfg Co | Reconstituted felt and manufacture of same |
-
1991
- 1991-12-10 CA CA002057474A patent/CA2057474A1/en not_active Abandoned
-
1992
- 1992-01-07 EP EP92610001A patent/EP0532445A1/en not_active Withdrawn
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6245388B1 (en) | 1999-06-30 | 2001-06-12 | The Chinet Company Technology | Wave coating of articles |
CN109629283A (en) * | 2018-12-05 | 2019-04-16 | 广东轻工职业技术学院 | A kind of paper idiosome and the preparation method and application thereof |
Also Published As
Publication number | Publication date |
---|---|
EP0532445A1 (en) | 1993-03-17 |
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Legal Events
Date | Code | Title | Description |
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EEER | Examination request | ||
FZDE | Discontinued | ||
FZDE | Discontinued |
Effective date: 19940612 |