US3020176A - Cast coated paper and method of making the same - Google Patents
Cast coated paper and method of making the same Download PDFInfo
- Publication number
- US3020176A US3020176A US721106A US72110658A US3020176A US 3020176 A US3020176 A US 3020176A US 721106 A US721106 A US 721106A US 72110658 A US72110658 A US 72110658A US 3020176 A US3020176 A US 3020176A
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- United States
- Prior art keywords
- coating
- casting surface
- cast
- water
- coated paper
- Prior art date
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- Expired - Lifetime
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- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 238000005266 casting Methods 0.000 claims description 54
- 238000000576 coating method Methods 0.000 claims description 54
- 239000011248 coating agent Substances 0.000 claims description 53
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 27
- 239000011707 mineral Substances 0.000 claims description 27
- 230000001112 coagulating effect Effects 0.000 claims description 21
- 239000007788 liquid Substances 0.000 claims description 15
- 239000003792 electrolyte Substances 0.000 claims description 14
- 238000000926 separation method Methods 0.000 claims description 12
- 239000002736 nonionic surfactant Substances 0.000 claims description 6
- VJYFKVYYMZPMAB-UHFFFAOYSA-N ethoprophos Chemical compound CCCSP(=O)(OCC)SCCC VJYFKVYYMZPMAB-UHFFFAOYSA-N 0.000 claims 1
- -1 as for example Substances 0.000 description 27
- 235000010755 mineral Nutrition 0.000 description 26
- 239000004094 surface-active agent Substances 0.000 description 25
- 238000000034 method Methods 0.000 description 24
- 239000003795 chemical substances by application Substances 0.000 description 20
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000000463 material Substances 0.000 description 13
- 239000000194 fatty acid Substances 0.000 description 12
- 230000008569 process Effects 0.000 description 11
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 10
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- 239000010408 film Substances 0.000 description 9
- 150000001408 amides Chemical class 0.000 description 8
- 239000000701 coagulant Substances 0.000 description 8
- 150000004665 fatty acids Chemical class 0.000 description 8
- 239000007795 chemical reaction product Substances 0.000 description 7
- 229920001223 polyethylene glycol Polymers 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 239000002202 Polyethylene glycol Substances 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- 102000004169 proteins and genes Human genes 0.000 description 6
- 239000008199 coating composition Substances 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 150000002170 ethers Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 239000011149 active material Substances 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- CBOCVOKPQGJKKJ-UHFFFAOYSA-L Calcium formate Chemical compound [Ca+2].[O-]C=O.[O-]C=O CBOCVOKPQGJKKJ-UHFFFAOYSA-L 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-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
- 229940044172 calcium formate Drugs 0.000 description 3
- 235000019255 calcium formate Nutrition 0.000 description 3
- 239000004281 calcium formate Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 239000008151 electrolyte solution Substances 0.000 description 3
- 229940021013 electrolyte solution Drugs 0.000 description 3
- 150000002193 fatty amides Chemical class 0.000 description 3
- 150000008379 phenol ethers Chemical class 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 229920001451 polypropylene glycol Polymers 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 235000010469 Glycine max Nutrition 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 229960003563 calcium carbonate Drugs 0.000 description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 239000008116 calcium stearate Substances 0.000 description 2
- 235000013539 calcium stearate Nutrition 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- UPYPTOCXMIWHSG-UHFFFAOYSA-N 1-dodecylsulfanyldodecane Chemical compound CCCCCCCCCCCCSCCCCCCCCCCCC UPYPTOCXMIWHSG-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
- 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 1
- 101100203600 Caenorhabditis elegans sor-1 gene Proteins 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 206010026749 Mania Diseases 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
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 241001148123 Salmonella enterica subsp. enterica serovar Essen Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 241000358472 Tenrec Species 0.000 description 1
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 229940010048 aluminum sulfate Drugs 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229960005069 calcium Drugs 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
- 239000001639 calcium acetate Substances 0.000 description 1
- 235000011092 calcium acetate Nutrition 0.000 description 1
- 229960005147 calcium acetate Drugs 0.000 description 1
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 description 1
- 239000001527 calcium lactate Substances 0.000 description 1
- 229960002401 calcium lactate Drugs 0.000 description 1
- 235000011086 calcium lactate Nutrition 0.000 description 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 230000006303 immediate early viral mRNA transcription Effects 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N methyl undecanoic acid Natural products CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- 239000011092 plastic-coated paper Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 235000012976 tarts Nutrition 0.000 description 1
- 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 1
- 239000004246 zinc acetate Substances 0.000 description 1
- 229960000314 zinc acetate Drugs 0.000 description 1
- 235000013904 zinc acetate Nutrition 0.000 description 1
Images
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
- 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
- D21H19/62—Macromolecular organic compounds or oligomers thereof obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31993—Of paper
Definitions
- This invention relates to the production of high gloss cast surfaced mineral coated papers, and more particularly to agents which are effective in providing ready and complete release of such coated papers from a casting surface.
- a difiiculty heretofore encountered in the production of cast-surfaced mineral-coated paper is sticking of the dried and set coating to the finishing surface, resulting in marring of the coated paper surface by particlesof the dried coating which adhere to the finishing surface. Indeed, this sticking may become so extreme that the entire area of the paper in contact with the finishing surface becomes tightly bonded thereto and is only removed by long and laborious treatment. Obviously, such a sticking condition makes the process of cast coating inoperable.
- oleaginousfilm forming materials which are characterized as relatively water-insoluble liquids which wet the casting surface. and spread into acontinuous film, yetwill not vaporize too readily at operating temperatures.
- the coating on the web is intended to .adhere firmly to the casting surface until the coating has dried to a non-plastic condition and is thereafter released from the casting surface. Satisfactory results utilizing this method allegedly are obtained only by periodic application of the oleaginous mate rial directly to. the casting surface, or, preferably, application of the oleaginous compound to the casting surface by incorporation of a quantity of the oleaginous release agent in the coating composition.
- this method is subject to the objection that the required function of oleaginous material on the casting surface is necessarily dependent on, and the exact quantity thereof determined by, a skilled operator who watches the point at which the paper leaves the casting surface, and hopefully increases or decreases the amount of oleaginous material on the chromium drum and/or in the coating composition in order to avoid sticking on the one hand, or loss of gloss in the finished paper on the other, the latter condition resulting from the use of an excess of oleaginous material.
- Another object of this invention is to provide an improved method for continuously producing cast surfaced mineral coated paper, which method facilitates ready release of coating from a casting surface.
- Another object is to provide water-soluble non-ionic surface active materials which have the property of readily effecting, separation of cast surfaced mineral coated paper from a casting surfaceon which it is dried.
- Another object is to provide a method of the foregoing type adapted to relatively high speed production.
- the release agents include certain water-soluble non-ionic surface active materials which are either normally liquid at room temperature, or become liquid at the operating temperature of the casting surface (which temperature varies with particular operating conditions, but normally falls in the range of 230 F.). Such agents have been found to be especially useful when added to the coagulant bath disclosed in copending application Serial No. 648,227, filed March 25, 1957 by John W. Smith, now U.S. Patent 2,950,214, and which is assigned to the same assignee as this application.
- an aqueous mineral coating composition comprising dispersed pigments and an adhesive is applied to a paper web in predetermined quantity and uniformly distributed thereon, and the coated surface of the web while still wet is thereafter contacted with a coagulant bath whereby the adhesive component of the freshly applied mineral coating is converted into a gel, without substantial drying, in a manner so as to prevent undesirable distortion of the coating film.
- the gelled coating is thereafter pressed against a casting surface and dried thereon.
- a paper web 11 to be coated is drawn from a supply roll 10 of suitable paper base stock and is led over guide rolls 12 and 13 to pass through the apparatus in the color applying zone.
- the web 11 passes through the nip of the coating application rolls 14, 15 where a predetermined amount of coating suspension is applied thereto and distributed with sutficient uniformity over the web surface to give the desired weight of coating material per unit area on the web.
- the coating color is fed through a suitable supply line and by suitable means to one or more discharge pipes or nozzles 23 and into the nip between rolls 15 and 24 which have the direction of rotation as indicated, the color forming a pool 25.
- the coated web is then brought with the coated side out tightly around roll 16 which dips into the coagulant and release agent bath of this invention contained in a tub 17.
- the coated paper 11 is then transferred by press roll 18, after the coating has been formed into a nontacky tough deformable gel, into nip 19, and thereby into contact with a heated finishing roll 20 having a smooth casting surface.
- the Web 11 remains in contact with casting roll 20 until the coating spontaneously releases after it has substantially completely dried and is removed by tension roll 21 to winder roll 22.
- the coating material generally comprises a mineral and an adhesive in-aqueons medium.
- a color formula which has been found to function satisfactorily in the practicing of the invention is of the following compdsitionQwherein the parts by weight are taken on a dry basis:
- Arrnnonia-ZS B (parts per 100 parts of protein) 120 Dow 512 R latex 4.0. Sodium pyrophosphaten fi '0.7'5 Calcium stearate' 0.57 Hy m e 2 i 0.05.
- Example V Calcium Carbonate 84.0 Alphapro tein I 12.0 Ammonia- 25 B. (parts per 100 parts of protein) 180 wnne C ium n
- Example VI Clay domestic coating clay 81.0 Soya protein (refined) 12.0
- the conversion of the adhesive component of-the' coating'to the gel state is almost instantaneous, requiring only a fraction of a second following initial-contact with the. coagulant.
- 'And mixing of the release agent of this invention with the coating composition is greatly restricted," and occurs to only a minor extent.
- the relea's'e' agent is carried on the surface of'the gelled coating'as a liquid solution (which'also contains the coagulant salts) to the casting nip.
- the film of re lease agent between the coating and'the' casting surface does not come into existence, until all or nearly allofxthcQ water present has been-evaporated.
- good contact and/or adherence of the wet, plastic coating to the casting surface is obtained, 'a condition desirable for attainment of a tr lyw ceststlrface of gloss approaching. that of the casting surface, but evaporation of' the water which sets the coating toanon-plastic state also serves unti h qoa nsha ee dried
- the coa ng, a ter ry-f ing, is readily, completely and cleanly separated from h s i u face.
- this invention provides for the formation of the releasing liquid film at the time and place of release from the casting surface, it is relatively free from a major limitation inherent in the use of the prior art oily or so-called oleaginous materials, in that the presence of an excess over the minimum required to provide ready release does not cause a loss of gloss in the cast-surfaced mineral coated paper, as is the case with said oleaginous materials.
- water soluble non-ionic surfactants could be employed as suitable release agents.
- materials such as water soluble reaction products of phenols, alcohols, higher fatty acids, amides, amines, propylene oxide, and/ or ethylene oxide were found to be especially suitable.
- water soluble surfactants is meant those surfactants which are self-dispersible in water and yield non-settling suspensions or clear solutions in water.
- water soluble non-ionic surfactants for the purpose of this invention are selected from the class comprising polymers of ethylene oxide and/or propylene oxide and their simple ethers
- agents selected from the following chemical classes of non-ionic surface active agents polymers of ethylene oxide and/or propylene oxide'and their simple ethers; esters of polyoxyethylene; polyethanolamine-fatty acid condensates; polyoxyethyl ene thio ethers; polyoxyethylene phenol ethers; substituted fatty amides; and polyoxyethylene amides.
- non-ionic water soluble surfactants of this invention are liquids or pastes at room temperature, but as mentioned hereinbefore, some of the effective materials are normally solid at room temperature, but melt and become liquid at or below the temperature of the casting surface, so that their function cannot be distinguished from that of the products which are normally liquids at room temperature.
- a typical coating composition comprising dispersed mineral pigments and an adhesive in aqueous medium was applied to apaper web in predetermined amount and spread to a uniform, smooth film thereon, as set forth anddiagrammatically shown in the copending application, supra.
- the wet, coated web without substantial drying, was then contacted on its coated side with a coagulating solution of calcium formate which also contained, one of the water soluble release agents of this invention.
- Glycol. glycol. 16 Polypropylene Glycol polypropylene glycol 1. 0 (1M. W. 1150 G1 1 W. i50). 1 1 1 0 17 Po yuropy ene yco p0 ypropy ene g yco (M. W. 425). (M. W. 425). 18 Ethofat 142/60 mono rod 011 fatty 1. 0
- polyoxyethylene polyoxyethylene sor- 1. 0
- bitan mono-oleate 0.5 do 0.25 polyethanolarnine- 1. 0
- the present invention includes all modifications and- 3&291175 sii cm w ich fal when the s ore o ten-rec witha casting surface, said surfactant being liquid on said casting surface and imparting substantially complete separation of said coating from. said casting surface.
- said surfactant being. selected from the group consisting of water-soluble: polymers of ethylene and propylene oxide and their simple ethers, esters of polyoxyethylene, polyethanolamine-fatty acid condensates, polyoxyethylene thio ethers, polyoxyethylene phenol ethers, substituted fatty amides and polyoxyethylene amides, and thereafter bringing said coating into contact with a casting surface,
- said surfactant being liquid on said casting surface and imparting substantially complete separation of said coating from said casting surface.
- said surfactant being selected from the water-soluble reaction products of phenols, alcohols, higher fatty acids, amides, aminesjmercaptans and propylene oxide respectively with ethylene oxide, andthereafter bringing said coating into contacttwith a casting surface, said surfactant being liquid on saidcasting surface and imparting sub-. standa y complete sepa ation of sa d c ating from said castina ur acc.
- t e surfactant consists essentially ofa. wateresoluble reaction nrc u ccf. ethyle e. o ide.
- the steps comprising coagulating thecoating while still mobile and fluent and deformable on the paper by direct contact with a coagulating electrolyte to form said coating into a tough deformable gel, concomitantly in oorporating a water-solublenon-ionic surfactant with said coagulating electrolyte which imparts substantially com plete separation of said coating from a casting surface,
- the concentration of said surfactant in the coagulating electrolyte being of the orderof 0.25 to 5.0%, and there: after bringing said coating into contact with a casting surface, said surfactant being liquid on said casting surface and imparting substantially complete separation of said coating from said casting surface.
- the steps comprising coagulating the coating while still mobile. and fluentiand deformable'on the paper by direct contact with a coagulating electrolyte. to form said coating into a tough deformable gel, concomitantlyim corporatinga non-ionic water-solublesurfactant with said coagulating electrolyte which impartssubstantially complete separation of said coating from a casting surface, said surfactant being selected from the water -.soluble,reaction productslofphcnols, alcohols, higher.
- a cast surfaced mineral coated paper substantially identical with the product obtainable by the process of claim 1.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paper (AREA)
Description
1952 J. v. ROBINSON ETAL 3,02
CAST COATED PAPER AND METHOD OF MAKING THE SAME Filed March 13, 1958 CASTING ROL L TENSION ROLL WINDE R ROL L JAMES V. ROBINSON, By EARL B. BROOKBANK, JR.
ATTORNEYs United States Patent Office 3,020,176 Patented Feb. .6, 1962 3,020,176 PAPER AND METHOD This invention relates to the production of high gloss cast surfaced mineral coated papers, and more particularly to agents which are effective in providing ready and complete release of such coated papers from a casting surface.
Various known methods of producingcast-surfaced mineral-coated papers are similar in that a wetand plastic coated paper is pressed into adherent contact with a finishing surface, such as a=highly polished chromium plated drum or belt, and dried thereon, and thereafter the dried coated paper is intended to separate from the drum with a surface finish which is desirably a replica of the finishing surface. A difiiculty heretofore encountered in the production of cast-surfaced mineral-coated paper is sticking of the dried and set coating to the finishing surface, resulting in marring of the coated paper surface by particlesof the dried coating which adhere to the finishing surface. Indeed, this sticking may become so extreme that the entire area of the paper in contact with the finishing surface becomes tightly bonded thereto and is only removed by long and laborious treatment. Obviously, such a sticking condition makes the process of cast coating inoperable.
Several methods have been proposed to substantially overcome this sticking of mineral coatings to the finishing surface. For example, one such method seeks to maintain on the finishing surface an invisible film, substantially less than 2000 Angstrom units in thickness, of oil or other fatty material, such substances being designated as oleaginousfilm forming materials, which are characterized as relatively water-insoluble liquids which wet the casting surface. and spread into acontinuous film, yetwill not vaporize too readily at operating temperatures. The coating on the web is intended to .adhere firmly to the casting surface until the coating has dried to a non-plastic condition and is thereafter released from the casting surface. Satisfactory results utilizing this method allegedly are obtained only by periodic application of the oleaginous mate rial directly to. the casting surface, or, preferably, application of the oleaginous compound to the casting surface by incorporation of a quantity of the oleaginous release agent in the coating composition.
Obviously, this method is subject to the objection that the required function of oleaginous material on the casting surface is necessarily dependent on, and the exact quantity thereof determined by, a skilled operator who watches the point at which the paper leaves the casting surface, and hopefully increases or decreases the amount of oleaginous material on the chromium drum and/or in the coating composition in order to avoid sticking on the one hand, or loss of gloss in the finished paper on the other, the latter condition resulting from the use of an excess of oleaginous material. Even a moderate increase in the thickness of the oleaginous film may cause a mottled appearance of the finished coated paper and may leave sufficient grease on the surface of the coated paper both to make the paper distasteful to handle and to produce Another object of this invention is to provide an improved method for continuously producing cast surfaced mineral coated paper, which method facilitates ready release of coating from a casting surface.
Another object is to provide water-soluble non-ionic surface active materials which have the property of readily effecting, separation of cast surfaced mineral coated paper from a casting surfaceon which it is dried.
It is a further object to provide such non-ionic surface active materials which are effective over a relatively wide range of concentrations.
Another object is to provide a method of the foregoing type adapted to relatively high speed production.
Numerous other objects of this invention will more fully hereinafter appear.
The sole figure of the drawing schematically illustrates one method of this invention. v t
The release agents, according to this invention, include certain water-soluble non-ionic surface active materials which are either normally liquid at room temperature, or become liquid at the operating temperature of the casting surface (which temperature varies with particular operating conditions, but normally falls in the range of 230 F.). Such agents have been found to be especially useful when added to the coagulant bath disclosed in copending application Serial No. 648,227, filed March 25, 1957 by John W. Smith, now U.S. Patent 2,950,214, and which is assigned to the same assignee as this application. According to the method therein disclosed for producing cast surfaced mineral coated paper, an aqueous mineral coating composition comprising dispersed pigments and an adhesive is applied to a paper web in predetermined quantity and uniformly distributed thereon, and the coated surface of the web while still wet is thereafter contacted with a coagulant bath whereby the adhesive component of the freshly applied mineral coating is converted into a gel, without substantial drying, in a manner so as to prevent undesirable distortion of the coating film. The gelled coating is thereafter pressed against a casting surface and dried thereon.
For example, reference is made to the accompanying drawing wherein a paper web 11 to be coated is drawn from a supply roll 10 of suitable paper base stock and is led over guide rolls 12 and 13 to pass through the apparatus in the color applying zone. The web 11 passes through the nip of the coating application rolls 14, 15 where a predetermined amount of coating suspension is applied thereto and distributed with sutficient uniformity over the web surface to give the desired weight of coating material per unit area on the web.
The coating color is fed through a suitable supply line and by suitable means to one or more discharge pipes or nozzles 23 and into the nip between rolls 15 and 24 which have the direction of rotation as indicated, the color forming a pool 25. Doctor 26, as shown, functions to maintain the pool in the nip between rolls 15 and 24 and any well known doctoring means may be employed.
The coated web is then brought with the coated side out tightly around roll 16 which dips into the coagulant and release agent bath of this invention contained in a tub 17. The coated paper 11 is then transferred by press roll 18, after the coating has been formed into a nontacky tough deformable gel, into nip 19, and thereby into contact with a heated finishing roll 20 having a smooth casting surface. The Web 11 remains in contact with casting roll 20 until the coating spontaneously releases after it has substantially completely dried and is removed by tension roll 21 to winder roll 22.
Various coating materials as described in the copending application, supra, may be employed in practicing the present'inventi'onand 'as indicated by "the formulations hereinafter 'set forth, the coating material generally comprises a mineral and an adhesive in-aqueons medium.
A color formula which has been found to function satisfactorily in the practicing of the invention is of the following compdsitionQwherein the parts by weight are taken on a dry basis:
Dow 5.12-R latex. (butadiene-styrene copolymer Di-isobutylphenoxyethoxyethyldimethylbenzyl-am moniur'nchloride,monohydrate (Hyamine 1622,
Rohm & Haas Co.) 005 Such color gives satisfactory results in the practicing of this invention when admixed with water to have a solids content of approximately 50.5%. i 1
The-following examples of color formulations which have likewise been used satisfactorily are set forth for purposes of illustration, but not of limitation; The parts by weight of these compositions are taken on a dry basis:
Example [I P rts y w i Clay (Eng i h o g cl y): 4 Calcium-carbonate I I i 42.0 Soya protein (refined) 12.0.
Arrnnonia-ZS B. (parts per 100 parts of protein) 120 Dow 512 R latex 4.0. Sodium pyrophosphaten fi '0.7'5 Calcium stearate' 0.57 Hy m e 2 i 0.05.
Examp e 1! Z "T" 'T '1"'TT'7' T-'T? 'T."'T bQ i T T' "J Ti"' T?'E'7 a h -9 Q "'7 "TT' 7T1'1T'"-ET--: -V mania-2636 (parts perlOO p ts of pro ein) 12.0 P w il eR'lat -0 od um r t n a h te. 1 In; stea et Leeann J 0.05:
xam e 1V Clay (English coating clay). Calcium. carbonate V, r p q i r-"xrr"7T"-1':--'r-r-:::- 1- z .(di yan am a s p r .0. parts of p otein) 25.0. Ammonia-26 B. (parts per 100 parts of protein) 12.0 Sodium pyrophosp'hate' 0.75 Calcium stearate 0.5 Lignasan I H 0.05
Example V Calcium Carbonate 84.0 Alphapro tein I 12.0 Ammonia- 25 B. (parts per 100 parts of protein) 180 wnne C ium n Example VI Clay (domestic coating clay) 81.0 Soya protein (refined) 12.0
Azite(dicyandiamide)(parts per parts of pron) y 25.0 Ammonia-26 B. (parts per 100 parts of protein) 15.0
As described in the copending application, supra, the conversion of the adhesive component of-the' coating'to the gel state is almost instantaneous, requiring only a fraction of a second following initial-contact with the. coagulant. 'And mixing of the release agent of this invention with the coating composition is greatly restricted," and occurs to only a minor extent. Thus,the relea's'e' agent is carried on the surface of'the gelled coating'as a liquid solution (which'also contains the coagulant salts) to the casting nip. A small quantity of this solu tion passes through the casting nip, together with thegelled coating, as a fluid film thereon, and is dried in contact with the casting surface, whereby the release agent is concentrated at the plane 'of release, and functions to provide clean separation of the cast coated web from the casting surface. Accordingly, incorporation ofthe water-soluble nonei'onie surface activerelease agents of this invention in the aforesaidcoaghlant bath insures the presence of the release 'age'ntat the point where needed to provide the desired function. Cast coated webs so prepared carry coatings-which are relatively free from contamination by release agents, the amount of such agent appearing in the cast coated paper being of the order of 0l0007 to 0101b. sa-moosq-rrrma pending on operating conditions and on the concentration" of the agent used in the coagulant bath which normally ranges from 0.125 to 5 .0% by weight, this in turn de pending on the particularrelea se agent'employedf While not wishing to be restricted thereby, it is believed that the mechanism by which such water-soluble" non-ionic surface active materials operate to provide re lease is concerned with the deposition of a very thin film of a liquid between the casting surfaceand the surface of the driedcoating, and that such a film, being of low cohesive strength, splits with one partrcrnaining'on' the paper and the other part remaining on the casting surface. According to'this mechanism, the film of re lease agent between the coating and'the' casting surface does not come into existence, until all or nearly allofxthcQ water present has been-evaporated. Thus; good contact and/or adherence of the wet, plastic coating to the casting surface is obtained, 'a condition desirable for attainment of a tr lyw ceststlrface of gloss approaching. that of the casting surface, but evaporation of' the water which sets the coating toanon-plastic state also serves unti h qoa nsha ee dried The coa ng, a ter ry-f ing, is readily, completely and cleanly separated from h s i u face. p e u ablyhe ause the p t n of the thinlayer of liq'uidfilm. deposited or formed be-. we t a i and ca ti u acev 'dfirin h n p n i ionrj -Since this invention provides for the formation of the releasing liquid film at the time and place of release from the casting surface, it is relatively free from a major limitation inherent in the use of the prior art oily or so-called oleaginous materials, in that the presence of an excess over the minimum required to provide ready release does not cause a loss of gloss in the cast-surfaced mineral coated paper, as is the case with said oleaginous materials.
In the development of this invention, it was discovered that a great number of water soluble non-ionic surfactants could be employed as suitable release agents. For example, materials such as water soluble reaction products of phenols, alcohols, higher fatty acids, amides, amines, propylene oxide, and/ or ethylene oxide were found to be especially suitable. By water soluble surfactants is meant those surfactants which are self-dispersible in water and yield non-settling suspensions or clear solutions in water. Such surfactants in the practice of this invention when incorporated with coagulating electrolyte solutions, as for example, calcium formate, retain their characteristics of solubility or suspension stability with no perceptible change.
While preferred water soluble non-ionic surfactants for the purpose of this invention are selected from the class comprising polymers of ethylene oxide and/or propylene oxide and their simple ethers, equally good results were obtained with agents selected from the following chemical classes of non-ionic surface active agents: polymers of ethylene oxide and/or propylene oxide'and their simple ethers; esters of polyoxyethylene; polyethanolamine-fatty acid condensates; polyoxyethyl ene thio ethers; polyoxyethylene phenol ethers; substituted fatty amides; and polyoxyethylene amides.
A considerable number of the non-ionic water soluble surfactants of this invention are liquids or pastes at room temperature, but as mentioned hereinbefore, some of the effective materials are normally solid at room temperature, but melt and become liquid at or below the temperature of the casting surface, so that their function cannot be distinguished from that of the products which are normally liquids at room temperature.
The invention will be more clearly understood by reference to the following examples, which serve to illustrate but not limit the scope of this invention.
In each of the examples set forth hereinafter, a typical coating composition, comprising dispersed mineral pigments and an adhesive in aqueous medium was applied to apaper web in predetermined amount and spread to a uniform, smooth film thereon, as set forth anddiagrammatically shown in the copending application, supra. The wet, coated web, without substantial drying, was then contacted on its coated side with a coagulating solution of calcium formate which also contained, one of the water soluble release agents of this invention. The web traveled to and was pressed against a highly polished chromium plated, heated casting drum, whereby a considerable portion of the coagulant and release surfactant which was carried on the surface of the web was squeezed from the surface by the action of the casting nip, which permitted only a relatively thin film of said solution to pass through on the surface of the gelled coating. Heat supplied to the interior of the drum, as by steam, evaporated the water from the gelled coating and from the layer of solution lying between the coating and the casting surface. In each case, the coated web, after reaching substantial dryness, separated easily and completely from the casting surface, and was observed to have a gloss closely approaching that of the polished casting surface. And except for the inclusion of the relatively water soluble release surfactants of this invention in the coagulating bath, the preferred procedure and apparatus used in the practice of this invention is the same as that disclosed in the referred to co -pending application, supra.
The following listing presents specific examples of commercially available water soluble, non-ionic surfactants, in the concentration set forth, which were used in the practice of this invention to efiect the desirable release as described hereinbefore.
. Concentration of Example Trade-name Composition Release Agent in Ooagulaut Solution 1 Ucon 50HB polyoxyethylene 1. 0
mouo-alkyl other. 2 fin d O. 5 3 do 0.25 4 Ucon 50HB 2000 1.0 5 o 0.5 6 Plurouic F-68 Polyoxyethylene 1. 0
ether of polyoxypropylene. 7 do do 0. 5 8 Tergitol XH polyalkylene glycol 1. 0
ether. 9 Tergitol XD. -.do 1. 0 10 Oarbowax 200 polyethylene glycol 1. 0
(M. W. 200). v 11 Oarbowax 600 polyethylene glycol 1.
(M. W. 600). 12 Carbowax 1000 polyethylene glycol 1. 0
(M. W. 1000). 13 Oarbowax 6000. polyethylene glycol 0. 5
(M. W. 6000). 14 Oarbowax 20M polyethylene glycol 0.5
(M. W. 2 000 15 lvIethoxypolyethylene methoxypolyethylene 1. 0
Glycol. glycol. 16 Polypropylene Glycol polypropylene glycol 1. 0 (1M. W. 1150 G1 1 W. i50). 1 1 1 0 17 Po yuropy ene yco p0 ypropy ene g yco (M. W. 425). (M. W. 425). 18 Ethofat 142/60 mono rod 011 fatty 1. 0
acid ester of polyoxyethylene. 19 do o 0.5 20 Ethofat 242/25 mono rosin fatty acid 1. 0
ester of polyoxyethylene. 21 Sterox GD tall oil fatty acid ester 1.0
of polyoxyethylene. 22 Nonisol 210 oleic acid ester of 5.0
polyoxyethylene. 23 Nonisol 300 stearic acid ester of 5.0
polyoxyethylene. lauric acid ester of 5. 0
polyoxyethylene. polyoxyethylene sor- 1. 0
bitan mono-oleate. 0.5 do 0.25 polyethanolarnine- 1. 0
fatty acid condensate. Alrosol B fatty alkylol amide 1. 0 condensate. Ninol 737 fatty acid alkanol 5. 0 amide. Nonic 234 polyethylene glycol 1.0
tart. dodecyl thioether. Nonic 218 do 1. 0 Nonic 260 --.-do 1.0 Polytergent G300 alkyl phenol poly- 1.0
glycol ether. 35- 0.5 36 IgepalOA 630 iso-octylphenoxypoly- 1. 0
oxycthylene ethanol. 37 Michelene DDS alkyl amido alcohol.-. 1. 0 38- 5.0 39 Michelene DLD fatty acid amide ester- 5. 0 40 Antarox G-lOO alkyl polyoxyethy; 5.0
lene ethanol amide.
All of the release agents in the above examples were found to be unaffected when used in combination with an electrolyte solution such as the electrolyte solution utilized for coagulation of the adhesive component of the coating mix. While the above stated examples were prepared in connection with a 5% calcium formate solution as the coagulant, the use of other electrolytes, such as calcium acetate, zinc acetate, calcium lactate, aluminum sulfate, and the like does not interfere with the proper functioning of the release agents of this invention.
Since the methods and products herein described are for the purpose of illustration only, it is to ire-understood that the present invention includes all modifications and- 3&291175 sii cm w ich fal when the s ore o ten-rec witha casting surface, said surfactant being liquid on said casting surface and imparting substantially complete separation of said coating from. said casting surface.
2. In the manufacture of cast-surfaced mineral coated paper, the steps comprising coagulating the coating while still mobile and fluent and deformable on the paper by direct contact with a coagulating electrolyte to form said ccating a tough, able. ge con omi nt y incorporating a water-soluble non-ionic surfactant with said coagulating electrolyte which imparts substantially complete separation of said coating from a casting surface,
said surfactant being. selected from the group consisting of water-soluble: polymers of ethylene and propylene oxide and their simple ethers, esters of polyoxyethylene, polyethanolamine-fatty acid condensates, polyoxyethylene thio ethers, polyoxyethylene phenol ethers, substituted fatty amides and polyoxyethylene amides, and thereafter bringing said coating into contact with a casting surface,
said surfactant being liquid on said casting surface and imparting substantially complete separation of said coating from said casting surface.
3. The process of producing a cast-surfaced mineral coated paper in-accordance with claim 2 wherein the surfactant consists essentially of water-soluble polymers of ethylene oxide and their simple ethers.
'4. The process of producing'a cast-surfaced mineral coated paper in accordance with claim 2 wherein the surfactant consists essentially of water-soluble polymers of ethylene oxidev and propylene oxide.
5. The process of producing aEaSt-surfaced mineral coated paperin accordancewith' claim2 wherein the surfactant consistsessentially of .watensolubleesters ofpolyoxyethylene. w
6. The process of producing a cast-surfaced mineral coated paper in accordance with claim 2 wherein the sur. faetant consists essentially of water-soluble polyoxyeth ylene phenol esters.
7. The process of producing a cast-surfaced mineralcoated paper'in accordance with claim 2 wherein the surfactant consists essentially of water-soluble p'olyoxyethy ic hexitancstcrs of at y c ds 8. In the manufacture of cast-surfaced mineral coated Pap the steps mp i coagu at n t e coating whil still mobile and fluent and deformable on the paper by d r ac with a oa ul n elec y to f rm. sai coating into a tough deformable gel, concomitantlyincorporating a n c r-soluble s rfactant. withsaid coagulating electrolyte which imparts substantially complete-separationof said coatingfrom a casting surface, said surfactant being selected from the water-soluble reaction products of phenols, alcohols, higher fatty acids, amides, aminesjmercaptans and propylene oxide respectively with ethylene oxide, andthereafter bringing said coating into contacttwith a casting surface, said surfactant being liquid on saidcasting surface and imparting sub-. standa y complete sepa ation of sa d c ating from said castina ur acc.
9 T e Pr c ss f Prod cing; ast-s rf ced mineral ated. pcri c o dan w th c a m. 8 herein. t e surfactant consists essentially ofa. wateresoluble reaction nrc u ccf. ethyle e. o ide.
19., The, P ce o producin ca t-surfa ed mineral.- qc tcdrzcrer. n ac cr aacew thclaim .8 wherein the an:-
ctant onsi s. essen al y o a a cr-so ubl rea tio product of ethylene oxide and propylene oxide 11. The process of producing a cast-surfaced mineral coated paper in accordance with claim 8 wherein the S1111. factant consists essentially of a water-soluble reaction product of ethylene oxide and alcohols.
12 The process of producing a cast-surfaced mineral coated paper in accordance with claim 8 wherein thesur: factant consists essentially of a water-soluble reaction product of ethylene oxide and fatty acids.
13. The process of producing a cast-surfaced mineral Q E 'P P I in 9 dance h l i 3 wherein he S1 1: factant consists essentially of a water-soluble reaction product of ethylene oxide, and hexitan essters. Y
14. The process of producing. a cast-surfacedmineral coated paper in accordance with claim 8 whereinthe surfactant consists essentially of a water-soluble reaction product of ethylene oxide and a phenol.
15. In the manufacture of cast-surfaced mineral coated paper, the steps comprising coagulating thecoating while still mobile and fluent and deformable on the paper by direct contact with a coagulating electrolyte to form said coating into a tough deformable gel, concomitantly in oorporating a water-solublenon-ionic surfactant with said coagulating electrolyte which imparts substantially com plete separation of said coating from a casting surface,
the concentration of said surfactant in the coagulating electrolyte being of the orderof 0.25 to 5.0%, and there: after bringing said coating into contact with a casting surface, said surfactant being liquid on said casting surface and imparting substantially complete separation of said coating from said casting surface.
16. In the manufacture of cast-surfaced mineral; coated paper, the steps comprising coagulating the coating while still mobile and fluent and deformable on the paper by direct contact with a coagulating electrolyte to form said coating. into a tough deformable gel, concomitantly in; corporating a water-soluble non-ionic surfactant withsaid coagulatingelectrolyte which imparts substantially cornpiete separation of said coating from a castingsurface, said surfactant being selected from the group consisting ofwater-soluble: polymers of ethylene and propylene oxide and their simple ethers, esters of polyoxyethylene, polyethanolamine-fatty acid condensates, polyoxyethylenc thio ethers, polyoxyethylene phenol ethers, substituted fatty amides and polyoxyethylene amides, the concern tration of said surfactant in the coagulating electrolyte being of the order of 0.25 to 5.0%, and thereafterbring-j ing said coating into contact'with a 'casting surface, said surfactant being liquid on saidcasting surface and imf parting substantially complete separation of said coating from said casting surface.
17. In the manufacture of cast-surfaced mineralcoated paper, the steps comprising coagulating the coating while still mobile. and fluentiand deformable'on the paper by direct contact with a coagulating electrolyte. to form said coating into a tough deformable gel, concomitantlyim corporatinga non-ionic water-solublesurfactant with said coagulating electrolyte which impartssubstantially complete separation of said coating from a casting surface, said surfactant being selected from the water -.soluble,reaction productslofphcnols, alcohols, higher. fatty acids, amides, amines, mercaptans and propylene oxide respectively with ethyleneoXidc, the concentration of the watersoluble reaction product in the coagulating electrolyte being of the order of 0.25 to. 5.0%, and thereafter bringing] saidcoating into contact with a casting surface, said'surfactant being liquid on said casting surface and imparting substantially complete separation of said coating from said casting surface. i
18. A cast surfaced mineral coated paper substantially identical with the product obtainable by the process of claim 1.
(References on. following. page) References Cited in the file of this patent UNITED STATES PATENTS Lunsted Apr. 6, 1954 Lunsted et a1 Sept. 20, 1955 5 Payne et a1 Jan. 10, 1956 10 Hart Nov. 6, 1956 McAuslan Dec. 4, 1956 Hart Jan. 1, 1957 Smith et a1 Jan. 7, 1958 Haas et a1. May 20, 1958
Claims (1)
1. IN THE MANUFACTURING OF CAST-SURFACES MINERAL COATED PAPER, THE STEP COMPRISING COAGULATING THE COATING WHILE STILL MOBILE AND FLUENT AND DEFORMABLE ON THE PAPER BY DIRECT CONTACT WITH A COAGULATING ELECTROLYTE TO FORM SAID COATING INTO A TOUGH DEFORMED GEL, CONCOMITANTLY INCORPORATING A WATER-SOLUABLE NON-IONIC SURFACTANT WITH SAID COAGULATING ELECTROLYTE WHICH IMPARTS SUBSTANTIALLY COMPLETE SEPERATION OF SAID COATONG FROM A CASTING SURFACE, AND THEREAFTER BRINGING SAID COATING INTO CONTACT WITH A CASTING SURFACE, SAID SULFACTANT BEING LIQUID ON SAID CASTING SURFACE AND IMPARTING SUBSTANTIALLY COMPLETE SEPARATION OF SAID COATING FROM SAID CASTING SURFACE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US721106A US3020176A (en) | 1958-03-13 | 1958-03-13 | Cast coated paper and method of making the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US721106A US3020176A (en) | 1958-03-13 | 1958-03-13 | Cast coated paper and method of making the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3020176A true US3020176A (en) | 1962-02-06 |
Family
ID=24896566
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US721106A Expired - Lifetime US3020176A (en) | 1958-03-13 | 1958-03-13 | Cast coated paper and method of making the same |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3020176A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3357844A (en) * | 1964-10-23 | 1967-12-12 | Crown Zellerbach Corp | Paper sizing lubricant composition comprising a fatty acid and non ionic lubricant |
| US3463659A (en) * | 1965-10-22 | 1969-08-26 | Oxford Paper Co | Vacuum metallized paper |
| US4109056A (en) * | 1975-05-05 | 1978-08-22 | Champion International Corporation | Starch/latex cast coatings for paper |
| US4380565A (en) * | 1982-01-08 | 1983-04-19 | Champion International Corporation | Color preservation of wax-coated paperboard |
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| US2674619A (en) * | 1953-10-19 | 1954-04-06 | Wyandotte Chemicals Corp | Polyoxyalkylene compounds |
| US2718509A (en) * | 1954-01-14 | 1955-09-20 | Wyandotte Chemicals Corp | Plasticized resin compositions |
| US2730531A (en) * | 1953-03-03 | 1956-01-10 | Shell Dev | Amides of epoxyamines |
| US2769725A (en) * | 1953-03-20 | 1956-11-06 | Warren S D Co | Method of cast calendering paper |
| US2773114A (en) * | 1954-08-31 | 1956-12-04 | Us Rubber Co | Battery separator and method of making same |
| US2776226A (en) * | 1955-04-27 | 1957-01-01 | Warren S D Co | Process of drum-finishing coated paper and product |
| US2819184A (en) * | 1953-10-22 | 1958-01-07 | Warren S D Co | Production of cast surfaced coated paper |
| US2835653A (en) * | 1953-03-19 | 1958-05-20 | Polaroid Corp | Polyoxyethylene substituted polymers and their preparation |
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Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2730531A (en) * | 1953-03-03 | 1956-01-10 | Shell Dev | Amides of epoxyamines |
| US2835653A (en) * | 1953-03-19 | 1958-05-20 | Polaroid Corp | Polyoxyethylene substituted polymers and their preparation |
| US2769725A (en) * | 1953-03-20 | 1956-11-06 | Warren S D Co | Method of cast calendering paper |
| US2674619A (en) * | 1953-10-19 | 1954-04-06 | Wyandotte Chemicals Corp | Polyoxyalkylene compounds |
| US2819184A (en) * | 1953-10-22 | 1958-01-07 | Warren S D Co | Production of cast surfaced coated paper |
| US2718509A (en) * | 1954-01-14 | 1955-09-20 | Wyandotte Chemicals Corp | Plasticized resin compositions |
| US2773114A (en) * | 1954-08-31 | 1956-12-04 | Us Rubber Co | Battery separator and method of making same |
| US2776226A (en) * | 1955-04-27 | 1957-01-01 | Warren S D Co | Process of drum-finishing coated paper and product |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3357844A (en) * | 1964-10-23 | 1967-12-12 | Crown Zellerbach Corp | Paper sizing lubricant composition comprising a fatty acid and non ionic lubricant |
| US3463659A (en) * | 1965-10-22 | 1969-08-26 | Oxford Paper Co | Vacuum metallized paper |
| US4109056A (en) * | 1975-05-05 | 1978-08-22 | Champion International Corporation | Starch/latex cast coatings for paper |
| US4380565A (en) * | 1982-01-08 | 1983-04-19 | Champion International Corporation | Color preservation of wax-coated paperboard |
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