US3316123A - Paper carrying non-blocking flexible grease-proof vinyl polymer coating - Google Patents
Paper carrying non-blocking flexible grease-proof vinyl polymer coating Download PDFInfo
- Publication number
- US3316123A US3316123A US341492A US34149264A US3316123A US 3316123 A US3316123 A US 3316123A US 341492 A US341492 A US 341492A US 34149264 A US34149264 A US 34149264A US 3316123 A US3316123 A US 3316123A
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- paper
- blocking
- weight
- copolymer
- ethyl acrylate
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- 238000000576 coating method Methods 0.000 title description 21
- 239000011248 coating agent Substances 0.000 title description 18
- 230000000903 blocking effect Effects 0.000 title description 15
- 229920002554 vinyl polymer Polymers 0.000 title description 5
- 229920001577 copolymer Polymers 0.000 claims description 29
- 229920001187 thermosetting polymer Polymers 0.000 claims description 21
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 15
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 15
- IWLBIFVMPLUHLK-UHFFFAOYSA-N azane;formaldehyde Chemical compound N.O=C IWLBIFVMPLUHLK-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 8
- 239000002981 blocking agent Substances 0.000 claims description 7
- 239000000839 emulsion Substances 0.000 description 15
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 13
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000004202 carbamide Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 239000004519 grease Substances 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 241000779819 Syncarpia glomulifera Species 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 239000001739 pinus spp. Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229940036248 turpentine Drugs 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920003180 amino resin Polymers 0.000 description 2
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 description 2
- 238000000149 argon plasma sintering Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- 241000233805 Phoenix Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- KLGBMDMPJKZWDX-UHFFFAOYSA-N [[4,6-bis(methoxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound COCNC1=NC(NCO)=NC(NCOC)=N1 KLGBMDMPJKZWDX-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- ZHNUHDYFZUAESO-OUBTZVSYSA-N aminoformaldehyde Chemical compound N[13CH]=O ZHNUHDYFZUAESO-OUBTZVSYSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- IRCAZSRWCCDLJN-UHFFFAOYSA-N ethyl prop-2-enoate;prop-2-enenitrile Chemical compound C=CC#N.CCOC(=O)C=C IRCAZSRWCCDLJN-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 235000021268 hot food Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000010409 thin film Substances 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
- D21H19/10—Coatings without pigments
- D21H19/14—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
- D21H19/24—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/26—Aminoplasts
-
- 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
- D21H19/10—Coatings without pigments
- D21H19/14—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
- D21H19/20—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained 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]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/3188—Next to cellulosic
- Y10T428/31895—Paper or wood
- Y10T428/31906—Ester, halide or nitrile of addition polymer
-
- 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]
- Y10T428/31942—Of aldehyde or ketone condensation product
- Y10T428/31949—Next to cellulosic
- Y10T428/31964—Paper
Definitions
- the present invention relates to paper carrying on either or both sides a non-adherent greaseand waterresistant coating which is non-blocking at elevated tem peratures. More particularly the invention relates to such paper coated with a homogeneous blend of an ethyl acrylate-acrylonitrile copolymer having a molecular weight in excess of about 1,000,000 and a thermoset amineformaldehyde resin, as more particularly described below.
- paper coated with a flexible copolymer of ethyl acrylate and acryolnitrile in weight ratio between about 4:1 and 6:5 is highly resistant to penetration by both grease and water making such paper particularly suited for fabrication into all'purpose containers, i.e., con-.
- tainers adapted to receive greasy and non-greasy liquids and solids at temperatures between about 0 C. and 100 C.
- Paper of the type mentioned is often wound into rolls before use, and it is not uncommon for the rolls to be stored or shipped under conditions where the paper reaches an elevated temperature. Moreover, it is not uncommon for cups, plates, etc., fabricated from such paper (or manufactured by coating preformed paper containers with an appropriate coating composition of the copolymer) to be subjected to elevated temperatures for similar reasons.
- a disadvantage of such paper is that before and after fabrication into useful articles it tends to block when maintained at elevated temperature, the layers or sheets adhering together because of the cohesiveness of the polymer. Paper which has blocked when stored in rolls tends to tear when unwound, and paper cups and plates which block tend to cause jamming when used in automatic apparatus dispensing hot food and drink.
- the paper of the present invention is conveniently made by forming an aqueous emulsion of the ethyl acrylateacrylonitrile copolymer, preferably by use of a sodium salt of a C -C mono (higher fatty alcohol) sulfate as emulsifying agent, adding one or more thermosetting amine-aldehyde resins thereto, applying the product to one or both sides of the paper, and drying the paper at a temperature where the deposited emulsion copolymer particles coalesce and the condensate thermosets.
- thermoset amino resin set in a matrix of the copolymer or the copolymer set in a matrix of the thermoset amino resin.
- the theory is presented for whatever help it may impart towards understanding the invention,
- the paper-coating ethyl acrylate-acrylonitrile copolymer referred to is the known flexible, greaseand waterresistant polymer prepared by copolymerizing ethyl acrylate and acrylonitrile in weight ratio between about 4:1 and 6:5, and may contain minor amounts (less than about 5% of the weight of the two principal components) of vinyl monomers copolymerizable therewith, for example acrylic acid, acrylamide, vinylidene chloride, styrene, etc., to improve the properties of the copolymer as regards emulsification and to stabilize the emulsions thereby.
- the amine-aldehyde condensate in the coating is a thermoset condensation product of an amidogen, for example melamine, urea, formoguanamine, thiourea, etc., with formaldehyde.
- an amidogen for example melamine, urea, formoguanamine, thiourea, etc.
- formaldehyde a suitable amidogen at an alkaline pH with about 1 mol of formaldehyde for every aldehyde-reactive amino group present and continuing the reaction, if desired, at an acid pH until the syrup has increased in viscosity while remaining hydrophilic.
- the copolymer being water-insoluble, is present as the dispersed phase and the hydrophilic amine-formaldehyde condensate is present in the aqueous phase.
- the emulsion need not contain an acid catalyst as the resins thermoset sufiiciently rapidly for papermaking purposes, and in fact the emulsion may have an alkaline pH.
- the viscosity of the emulsion chiefly depends upon the proportion of water present and is adjusted so as to fall within the range required by the particular coating method employed.
- the emulsion may be applied as a spray, or by doctor blade, off-set roll, or knife-coater, and is applied in suificient thickness so that the final (dry) film weighs 1.5 to 1 lb. per 1000 ft. of paper.
- the final step in the process is the heating of the paper until the deposited polymer particles have coalesced and the amine-formaldehyde condensate has thermoset ⁇
- the optimum heating temperature and. the duration of the heating depend primarily upon the thermosetting characteristics of the particular amine-aldehyde resin employed and in each specific instance are most conveniently found by trial. It is preferred to heat the sheets at a temperature between about 220 F. and. 300 F. for two minutes to five minutes as in this range the anti-blocking characteristics of the composition are developed without harm to the fibers.
- the invention is more particularly illustrated by the drawing which is a schematic vertical section of paper coated with a mixture of ethyl acrylate-acrylonitrile copolymer and a thermoset amine-aldehyde condensate.
- Example 1 The following illustrates the effectiveness of amineformaldehyde condensate in decreasing the high-temperature adhesiveness of paper coated with ethyl acrylateacrylonitrile copolymer.
- a series of coated papers were prepared on 50 lb. basis weight x "/500 ream) stock by applying to one side of each sheet the ethyl acrylate-acrylonitrile emulsions with and without a thermosetting amine-aldehyde resin, as shown in the table below.
- the emulsions were applied at a thickness equivalent to 1.5 lbs. of resin sollds per 1,000 square feet of paper surface by means of a 0.0005" Bird applicator at 40% resin solids.
- the paper samples were air dried and then heated in a circulating air oven for 2 minutes at 300 F. to cause the copolymer particles to fuse and the amine-aldehyde resin, where pressent, to thermoset.
- the resin coatings were tested for blocking by the following modification of TAPPI standard T477m47.
- Squares 1" x 1" were cut from the coated paper samples and stacked in a constant temperature oven and a 1 lb. steel weight 1 x 1" in area was placed on top. The oven was maintained at 170 F. for 16 hours, at the end of which time the stack was separated into its components and the tendency of each pair of squares to block was noted.
- a blocking rating of 3 designates strong adhesion so that the coating is extensively torn when the sheets are peeled apart.
- a blocking rating of 2 designates local or slight adhesion of the coating so that only slight picking or marring occurs when the sheets are peeled apart.
- a blocking rating of 1 designates no actual adhesion but an affinity such that the surfaces do not sli-de freely against each other, or an audible tick is heard when the sheets are peeled apart.
- a blocking rating of 0 designates separation of the surfaces without adhesion or tick, that is, as if the surfaces were enameled so that they fall apart.
- the emulsions were prepared by emulsion copolymerizing ethyl acrylate and acrylonitrile in 70:30 weight ratio in water containing catalyst and emulsifying agent [Du- One portion of the product was reserved as control and to this nothing was added. To the remaining portions were added sufficient of 40% by weight aqueous solutions of a melamineformaldehyde condensation [di (methoxymethyl) hyroxymethymelarnine] and a urea-formaldehyde condensate (the urea-formaldehyde-bisulfite resin of US. Patent No. 2,559,578) to supply the proportions of these resins shown in the table below.
- Example 2 Coated paper was prepared by repetition of the method of Example 1 except that the latex was applied from a 0.0003 Bird applicator, the coating being equivalent to about 1.25 lbs. of total resin solids per 1,000 sq. ft. of paper, the latex being applied as a double coating to give this thickness of resin.
- the paper sheets were dried according to the method of Example 1 and were tested for grease resistance according to TAPPI Standards Test T454m44, wherein small (approximately 5 gm.) cones of sand are formed on the paper and grease resistance is determined as the number of minutes required for 1.1 ml. of turpentine (containing an oil soluble red dye) added to each cone to penetrate the sheet.
- the endpoint of the test is the time for first penetration, and observations are discontinued after 480 minutes because of evaporation of turpentine.
- resistance of coating material at the very thin film thickness described above to penetration by turpentine for the full 480 minute period is regarded as excellent.
- Type Percent 1 Based on weight of ethyl acrylate-acrylonitrile copolymer. 2 Control.
- Example 3 The following illustrates the decreased blocking possessed by cups formed of paper according to the present invention after nesting at elevated temperature under weight.
- a number of uncoate'd paper cups were half-filled with the emulsion of Example 1 wherein the amino-aldehyde resin was di(methoxymethyl) hydroxymethylmelamine, slowly spun so as to coat theinterior surface of the cups with the emulsion, emptied, and then spun at 1700 rpm. to remove excess emulsion.
- the cups were then oven dried for 2 minutes at 300 F. and had uniformly coated interiors and lips.
- the cups were nested and tested in groups of five, the top cup in each stack being weighted with sufficient sand so that the bottom cup sustained a weight equal to the weight of 49 cups.
- the stacks of cups were placed in an oven at F. for 24 hours and blocking values were assigned by lifting the stacks, releasing the cups consecutively from the bottom, and averaging the results.
- the block ratings assigned correspond to those of Example 1.
- Example 4 It is necessary that the molecular weight of the copoly- Percent Rating Run N 0. Copolymer Amine Sheet Assembly Block Molec. Wt. CHzO Test 3 Resin 700, 000 50 Face to face 2+ 700,000 65 do 2 1, 300, 000 50 0 1, 300, 000 0+ 1 Weight average molecular weight determined at and for each of six solution concentrations, by procedure of Stacey Light Scattering in Physical Chemistry, Academic Press, N.Y., 1956, and Brice-Phoenix Light Scattering Photometer Operation Manua OM-lOOO, Phoenix Precision Instrument 00., Philadelphia, Pa., 1955.
- Comparison of run 1 with run 2 shows that coatings wherein the copolymer has a molecular weight substantially below 1,000,000 possess very significant blocking properties, and that these blocking properties are not significantly affected by a substantial increase in the amount of amine-aldehyde.
- Run 4 shows that it is the molecular weight which is of primary significance because the block test rating of the coating does not significantly change even when the amount of amine-aldehyde resin in the coating is greatly decreased.
- Paper coated on at least one side with a flexible uniform greaseand water-resistant composition consisting essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 4:1 and 6:5 to a molecular weight in excess of 1,000,000, and a thermoset amineformaldehyde condensate in amount between 10% and 75% of the Weight of said ethyl acrylate and acrylonitrile copolymer as anti-blocking agent.
- a flexible uniform greaseand water-resistant composition consist- 6 ing essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 3:1 and 3:2 to a molecular weight in excess of 1,000,000, and a thermoset amineformaldehyde condensate in amount between 10% and 75% of the weight of said ethyl acrylate and acrylonitrile copolymer as anti-blocking agent.
- Paper coated on at least one side with a flexible uniform greaseand water-resistant composition consisting essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 3 :1 and 3:2 to a molecular weight in excess of 1,000,000, and a thermoset melamineformaldehyde condensate in amount between 10% and 75 of the weight of said ethyl acrylate and acrylonitrile copolymer as anti-blocking agent.
- Paper coated on at least one side with a flexible uniform greaseand water-resistant composition consisting essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 4:1 and 6:5, a thermoset amine-formaldehyde condensate in amount between 10% and 75 of the weight of said ethyl acrylate and acrylonitrile copolymer, and a sodium salt of a C -C mono (higher fatty alcohol) sulfate as secondary anti-blocking agent.
- a flexible uniform greaseand water-resistant composition consisting essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 4:1 and 6:5, a thermoset amine-formaldehyde condensate in amount between 10% and 75 of the weight of said ethyl acrylate and acrylonitrile copolymer, and a sodium salt of a C -C mono (higher fatty alcohol) sulfate as secondary anti-blocking
- Paper coated on at least one side with a flexible uniform greaseand water-resistant composition consisting essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 4:1 and 6:5, a thermoset amine-formaldehyde condensate in amount between 10% and 75 of the weight of said ethyl acrylate and acrylonitrile copolymer, and sodium lauryl sulfate as secondary anti-blocking agent.
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Description
Apnl 25, 1967 A. R. SAVINA ET AL 3,316,123
PAPER CARRYING NONBLOCKING FLEXIBLE GREASE-PROOF VINYL POLYMER COATING Filed Jan. 28, 1964 MIXTURE 0F ETHYL ACRYLATE-ACRYLONITRILE COPOLYMER 'AND THERMOSET AMlNE-ALDEHYDE CONDENSATE ANTHONY R. SAVINA DANIEL D. RITSON IN V EN TORS A r ran/vs? United States Patent 6 3,316,123 PAPER CARRYING NON-BLOCKING FLEXIBLE GREASE-PROOF VINYL POLYMER COATING Anthony Ralph Savina, Stamford, and Daniel Dickerson Ritson, Riverside, Conn, assignors to American'Cyanamid Company, Stamford, Conn., a corporation of Maine Filed Jan. 28, 1964, Ser. No. 341,492 5 Claims. (Cl. 117-155) This is a continuation-in-part of our copending applications Ser. Nos. 794,525 and 282,194, respectively filed on Feb. 20, 1959, and on May 15, 1963, and now abandoned.
The present invention relates to paper carrying on either or both sides a non-adherent greaseand waterresistant coating which is non-blocking at elevated tem peratures. More particularly the invention relates to such paper coated with a homogeneous blend of an ethyl acrylate-acrylonitrile copolymer having a molecular weight in excess of about 1,000,000 and a thermoset amineformaldehyde resin, as more particularly described below.
It is known that paper coated with a flexible copolymer of ethyl acrylate and acryolnitrile in weight ratio between about 4:1 and 6:5 is highly resistant to penetration by both grease and water making such paper particularly suited for fabrication into all'purpose containers, i.e., con-.
tainers adapted to receive greasy and non-greasy liquids and solids at temperatures between about 0 C. and 100 C.
Paper of the type mentioned is often wound into rolls before use, and it is not uncommon for the rolls to be stored or shipped under conditions where the paper reaches an elevated temperature. Moreover, it is not uncommon for cups, plates, etc., fabricated from such paper (or manufactured by coating preformed paper containers with an appropriate coating composition of the copolymer) to be subjected to elevated temperatures for similar reasons.
A disadvantage of such paper is that before and after fabrication into useful articles it tends to block when maintained at elevated temperature, the layers or sheets adhering together because of the cohesiveness of the polymer. Paper which has blocked when stored in rolls tends to tear when unwound, and paper cups and plates which block tend to cause jamming when used in automatic apparatus dispensing hot food and drink.
The discovery has now been made that paper coated with a flexible greaseand water-resistant ethyl acrylateacrylonitrile copolymer having a molecular weight in excess of about 1,000,000 possesses substantially no tendency towards blocking, even when maintained at temperatures as high as 190 F. for protracted periods of time, when the coating has a uniform substantial content of a thermoset amine-formaldehyde condensate.
The paper of the present invention is conveniently made by forming an aqueous emulsion of the ethyl acrylateacrylonitrile copolymer, preferably by use of a sodium salt of a C -C mono (higher fatty alcohol) sulfate as emulsifying agent, adding one or more thermosetting amine-aldehyde resins thereto, applying the product to one or both sides of the paper, and drying the paper at a temperature where the deposited emulsion copolymer particles coalesce and the condensate thermosets.
The structure of the coating on the paper has not been ascertained, but according to one theory it consists essentially of the thermoset amino resin set in a matrix of the copolymer, or the copolymer set in a matrix of the thermoset amino resin. The theory is presented for whatever help it may impart towards understanding the invention,
and the invention does not depend on whether or not the theory is correct.
The paper-coating ethyl acrylate-acrylonitrile copolymer referred to is the known flexible, greaseand waterresistant polymer prepared by copolymerizing ethyl acrylate and acrylonitrile in weight ratio between about 4:1 and 6:5, and may contain minor amounts (less than about 5% of the weight of the two principal components) of vinyl monomers copolymerizable therewith, for example acrylic acid, acrylamide, vinylidene chloride, styrene, etc., to improve the properties of the copolymer as regards emulsification and to stabilize the emulsions thereby.
The amine-aldehyde condensate in the coating is a thermoset condensation product of an amidogen, for example melamine, urea, formoguanamine, thiourea, etc., with formaldehyde. Such condensates may be prepared by reacting a suitable amidogen at an alkaline pH with about 1 mol of formaldehyde for every aldehyde-reactive amino group present and continuing the reaction, if desired, at an acid pH until the syrup has increased in viscosity while remaining hydrophilic.
In the paper-coating emulsion the copolymer, being water-insoluble, is present as the dispersed phase and the hydrophilic amine-formaldehyde condensate is present in the aqueous phase. The emulsion need not contain an acid catalyst as the resins thermoset sufiiciently rapidly for papermaking purposes, and in fact the emulsion may have an alkaline pH.
The viscosity of the emulsion chiefly depends upon the proportion of water present and is adjusted so as to fall within the range required by the particular coating method employed. The emulsion may be applied as a spray, or by doctor blade, off-set roll, or knife-coater, and is applied in suificient thickness so that the final (dry) film weighs 1.5 to 1 lb. per 1000 ft. of paper.
The final step in the process is the heating of the paper until the deposited polymer particles have coalesced and the amine-formaldehyde condensate has thermoset} The optimum heating temperature and. the duration of the heating depend primarily upon the thermosetting characteristics of the particular amine-aldehyde resin employed and in each specific instance are most conveniently found by trial. It is preferred to heat the sheets at a temperature between about 220 F. and. 300 F. for two minutes to five minutes as in this range the anti-blocking characteristics of the composition are developed without harm to the fibers.
Laboratory trials have shown that the presence of as little as 10% of the amine-formaldehyde condensate, based on the weight of the copolymer, improves the blocking characteristics of the copolymer, so that evidently a still smaller amount will impart some benefit. At the other extreme we have found it unnecessary for most practical applications to employ more than of the condensate on the same basis, and the suitable amount in any one instance is most easily found by trial within or without the range mentioned.
In practice we prefer suificient of the amino-formaldehyde condensate to give the coating composition a blocking rating of zero when tested under a pressure of 1 lb./in. for 16 hours at F. as this amount generally ensures that nested articles fabricated from this paper will separate readily when used in automatic dispensing equipment at elevated temperatures.
The invention is more particularly illustrated by the drawing which is a schematic vertical section of paper coated with a mixture of ethyl acrylate-acrylonitrile copolymer and a thermoset amine-aldehyde condensate.
The invention is more particularly described in the examples which follow. These examples constitute embodiponal C (sodium lauryl sulfate)].
ments of the invention and are not to be construed as limitations thereon.
Example 1 The following illustrates the effectiveness of amineformaldehyde condensate in decreasing the high-temperature adhesiveness of paper coated with ethyl acrylateacrylonitrile copolymer.
A series of coated papers were prepared on 50 lb. basis weight x "/500 ream) stock by applying to one side of each sheet the ethyl acrylate-acrylonitrile emulsions with and without a thermosetting amine-aldehyde resin, as shown in the table below. The emulsions were applied at a thickness equivalent to 1.5 lbs. of resin sollds per 1,000 square feet of paper surface by means of a 0.0005" Bird applicator at 40% resin solids. The paper samples were air dried and then heated in a circulating air oven for 2 minutes at 300 F. to cause the copolymer particles to fuse and the amine-aldehyde resin, where pressent, to thermoset.
The resin coatings were tested for blocking by the following modification of TAPPI standard T477m47.
Squares 1" x 1" were cut from the coated paper samples and stacked in a constant temperature oven and a 1 lb. steel weight 1 x 1" in area was placed on top. The oven was maintained at 170 F. for 16 hours, at the end of which time the stack was separated into its components and the tendency of each pair of squares to block was noted. A blocking rating of 3 designates strong adhesion so that the coating is extensively torn when the sheets are peeled apart. A blocking rating of 2 designates local or slight adhesion of the coating so that only slight picking or marring occurs when the sheets are peeled apart. A blocking rating of 1 designates no actual adhesion but an affinity such that the surfaces do not sli-de freely against each other, or an audible tick is heard when the sheets are peeled apart. A blocking rating of 0 designates separation of the surfaces without adhesion or tick, that is, as if the surfaces were enameled so that they fall apart.
The emulsions were prepared by emulsion copolymerizing ethyl acrylate and acrylonitrile in 70:30 weight ratio in water containing catalyst and emulsifying agent [Du- One portion of the product was reserved as control and to this nothing was added. To the remaining portions were added sufficient of 40% by weight aqueous solutions of a melamineformaldehyde condensation [di (methoxymethyl) hyroxymethymelarnine] and a urea-formaldehyde condensate (the urea-formaldehyde-bisulfite resin of US. Patent No. 2,559,578) to supply the proportions of these resins shown in the table below.
Results were as follows:
Amine CI-I O Block Test, 1 lh./in. Run Resin 16 hrs. N0. Sheet Assembly Type Percent 1 Temp, F. Rating 1 AL". Face to face None 170 2 Face to back None 170 2 Face to face"... Mel... 25 170 0+ Face to back. Mel... 25 170 0 Face to face... Mel. 170 0 Face to back Mel 50 170 0 Face to face... Urea 25 170 0 Face to back Urea" 25 170 0 Face to face. Urea 50 170 0 Face to baelL... Urea" 50 170 0 Face to face Urea 190 0 1 Based on the weight of ethyl acrylate-acrylonitrile copolymer. 1 See text above. 3 Controls.
Similar results are obtained by use of other sodium salts of C C mono(higher fatty alcohol) sulfates. These sulfate ester-salts are present in the vinyl coating composition and act as secondary anti-blocking agents, enhancing the primary anti-blocking effect produced by the thermoset amine-formaldehyde condensate.
4- Example 2 Coated paper was prepared by repetition of the method of Example 1 except that the latex was applied from a 0.0003 Bird applicator, the coating being equivalent to about 1.25 lbs. of total resin solids per 1,000 sq. ft. of paper, the latex being applied as a double coating to give this thickness of resin.
The paper sheets were dried according to the method of Example 1 and were tested for grease resistance according to TAPPI Standards Test T454m44, wherein small (approximately 5 gm.) cones of sand are formed on the paper and grease resistance is determined as the number of minutes required for 1.1 ml. of turpentine (containing an oil soluble red dye) added to each cone to penetrate the sheet. The endpoint of the test is the time for first penetration, and observations are discontinued after 480 minutes because of evaporation of turpentine. In this test, resistance of coating material at the very thin film thickness described above to penetration by turpentine for the full 480 minute period is regarded as excellent.
Results were as follows:
Amino CHgO Resin Grease Resist Run No.
(minutes) Type Percent 1 1 Based on weight of ethyl acrylate-acrylonitrile copolymer. 2 Control.
Example 3 The following illustrates the decreased blocking possessed by cups formed of paper according to the present invention after nesting at elevated temperature under weight.
A number of uncoate'd paper cups were half-filled with the emulsion of Example 1 wherein the amino-aldehyde resin was di(methoxymethyl) hydroxymethylmelamine, slowly spun so as to coat theinterior surface of the cups with the emulsion, emptied, and then spun at 1700 rpm. to remove excess emulsion. The cups were then oven dried for 2 minutes at 300 F. and had uniformly coated interiors and lips.
The cups were nested and tested in groups of five, the top cup in each stack being weighted with sufficient sand so that the bottom cup sustained a weight equal to the weight of 49 cups. The stacks of cups were placed in an oven at F. for 24 hours and blocking values were assigned by lifting the stacks, releasing the cups consecutively from the bottom, and averaging the results. The block ratings assigned correspond to those of Example 1.
Percent Mel. GH O Block Test Run No. Resin l (50 cup eqniv., 190 F., 24 hrs.)
None 2 25 1 50 O 1 Based on the weight of ethyl acrylate-acrylonitrlle copolymer. Z Control.
Example 4 It is necessary that the molecular weight of the copoly- Percent Rating Run N 0. Copolymer Amine Sheet Assembly Block Molec. Wt. CHzO Test 3 Resin 700, 000 50 Face to face 2+ 700,000 65 do 2 1, 300, 000 50 0 1, 300, 000 0+ 1 Weight average molecular weight determined at and for each of six solution concentrations, by procedure of Stacey Light Scattering in Physical Chemistry, Academic Press, N.Y., 1956, and Brice-Phoenix Light Scattering Photometer Operation Manua OM-lOOO, Phoenix Precision Instrument 00., Philadelphia, Pa., 1955.
2 Based on weight of copolymer.
3 By method of Example 1.
Comparison of run 1 with run 2 shows that coatings wherein the copolymer has a molecular weight substantially below 1,000,000 possess very significant blocking properties, and that these blocking properties are not significantly affected by a substantial increase in the amount of amine-aldehyde.
Comparison of these runs with run 3 show that the blocking problem substantially disappears when the copolymer in the coating has a molecular weight in excess of 1,000,000. Run 4 shows that it is the molecular weight which is of primary significance because the block test rating of the coating does not significantly change even when the amount of amine-aldehyde resin in the coating is greatly decreased.
What is claimed is:
1. Paper coated on at least one side with a flexible uniform greaseand water-resistant composition consisting essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 4:1 and 6:5 to a molecular weight in excess of 1,000,000, and a thermoset amineformaldehyde condensate in amount between 10% and 75% of the Weight of said ethyl acrylate and acrylonitrile copolymer as anti-blocking agent.
2. Paper coated on at least one side with a flexible uniform greaseand water-resistant composition consist- 6 ing essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 3:1 and 3:2 to a molecular weight in excess of 1,000,000, and a thermoset amineformaldehyde condensate in amount between 10% and 75% of the weight of said ethyl acrylate and acrylonitrile copolymer as anti-blocking agent.
3. Paper coated on at least one side with a flexible uniform greaseand water-resistant composition consisting essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 3 :1 and 3:2 to a molecular weight in excess of 1,000,000, and a thermoset melamineformaldehyde condensate in amount between 10% and 75 of the weight of said ethyl acrylate and acrylonitrile copolymer as anti-blocking agent.
4. Paper coated on at least one side with a flexible uniform greaseand water-resistant composition consisting essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 4:1 and 6:5, a thermoset amine-formaldehyde condensate in amount between 10% and 75 of the weight of said ethyl acrylate and acrylonitrile copolymer, and a sodium salt of a C -C mono (higher fatty alcohol) sulfate as secondary anti-blocking agent.
5. Paper coated on at least one side with a flexible uniform greaseand water-resistant composition consisting essentially of ethyl acrylate and acrylonitrile copolymerized in weight ratio between 4:1 and 6:5, a thermoset amine-formaldehyde condensate in amount between 10% and 75 of the weight of said ethyl acrylate and acrylonitrile copolymer, and sodium lauryl sulfate as secondary anti-blocking agent.
Retereuces Cited by the Examiner UNITED STATES PATENTS 2,299,805 10/ 1942 Denman 117-155 X 2,482,499 9/1949 Nagel 117-155 X 2,536,050 1/1951 Fluck.
2,537,019 1/1951 Barrett 260-452 X 2,559,234 7/1951 Stearn 117-155 2,708,645 5/1955 Norman 117-155 2,772,184 11/1956 Wolfe et al. 117-155 X 2,787,603 4/1957 Sanders 117-128.4 X 2,805,621 9/1957 Pickrel 117-155 X 2,866,763 12/1958 Sanders 260-851 X 2,889,299 6/1959 Ritson 117-155 X 2,922,732 1/1960 Hopkins et a1.
3,015,578 2/1962 Ritson.
WILLIAM D. MARTIN, Primary Examiner. M. R. LUSIGNAN, Assistant Examiner.
Claims (1)
1. PAPER COATED ON AT LEAST ONE SIDE WITH A FLEXIBLE UNIFORM GREASE- AND WATER-RESISTANT COMPOSITION CONSISTING ESSENTIALLY OF ETHYL ACRYLATE AND ACRYLONITRILE COMPOLYMERIZED IN WEIGHT RATIO BETWEEN 4:1 AND 6:5 TO A MOLECULAR WEIGHT IN EXCESS OF 1,000,000, AND A THERMOSET AMINEFORMALDEHYDE CONDENSATE IN AMOUNT BETWEEN 10% AND 75% OF THE WEIGHT OF SAID ETHYL ACRYLATE AND ACRYLONITRILE COPOLYMER AS ANTI-BLOCKING AGENT.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US341492A US3316123A (en) | 1964-01-28 | 1964-01-28 | Paper carrying non-blocking flexible grease-proof vinyl polymer coating |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US341492A US3316123A (en) | 1964-01-28 | 1964-01-28 | Paper carrying non-blocking flexible grease-proof vinyl polymer coating |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3316123A true US3316123A (en) | 1967-04-25 |
Family
ID=23337799
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US341492A Expired - Lifetime US3316123A (en) | 1964-01-28 | 1964-01-28 | Paper carrying non-blocking flexible grease-proof vinyl polymer coating |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3316123A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3442730A (en) * | 1965-09-13 | 1969-05-06 | Johns Manville | Preformed floor surface article and method of applying same |
| US3489706A (en) * | 1967-05-16 | 1970-01-13 | Goodrich Co B F | Bis(beta-chloroethyl)vinyl phosphonate copolymer compositions |
| US3676410A (en) * | 1970-08-24 | 1972-07-11 | Goodyear Tire & Rubber | Ethylhexyl acrylate-acrylonitrile-divinylbenzene terpolymers |
| US3772061A (en) * | 1971-10-14 | 1973-11-13 | Liberty Glass Co | Containers and methods of preparing |
| US3984594A (en) * | 1973-08-29 | 1976-10-05 | Kanebo, Ltd. | Method for producing cellulosic fiber-containing yarns with a non-aqueous sizing solution |
| EP4122988A1 (en) | 2021-07-23 | 2023-01-25 | Cargill, Incorporated | Water based barrier coating |
Citations (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2299805A (en) * | 1941-12-26 | 1942-10-27 | Detroit Gasket & Mfg Company | Packing |
| US2482499A (en) * | 1946-05-21 | 1949-09-20 | Westinghouse Electric Corp | Laminates embodying mixed phenolarylamine-formaldehyde resinous products |
| US2536050A (en) * | 1947-11-10 | 1951-01-02 | American Cyanamid Co | Treatment of cellulosic textile materials and products thereof |
| US2537019A (en) * | 1948-05-29 | 1951-01-09 | Monsanto Chemicals | Coating compositions |
| US2559234A (en) * | 1945-02-16 | 1951-07-03 | John T Stearn | Process of treating paper |
| US2708645A (en) * | 1952-04-19 | 1955-05-17 | Globe Envelopes Ltd | Method of making coated paper receptacles |
| US2772184A (en) * | 1953-09-21 | 1956-11-27 | Kimberly Clark Co | Paper coating |
| US2787603A (en) * | 1953-07-23 | 1957-04-02 | Du Pont | Aqueous coating compositions and substrates coated therewith |
| US2805621A (en) * | 1954-02-10 | 1957-09-10 | Standard Register Co | Paper planographic plate |
| US2866763A (en) * | 1956-04-16 | 1958-12-30 | Du Pont | Process of preparing aqueous dispersion of an acrylonitrile interpolymer and a thermosetting resin and product obtained |
| US2889299A (en) * | 1957-07-19 | 1959-06-02 | American Cyanamid Co | Grease resistant cellulosic webs coated with a linear anionic thermoplastic ethyl acrylate-acrylonitrile-methacrylic acid polymer containing a hydrophilic inorganic pigment as extender and composition for manufacture thereof |
| US2922732A (en) * | 1955-08-12 | 1960-01-26 | Rohm & Haas | Fiber-reinforced resin-bearing tissues, films or sheets, and articles obtained therefrom |
| US3015578A (en) * | 1958-03-25 | 1962-01-02 | American Cyanamid Co | Two-sided paper |
-
1964
- 1964-01-28 US US341492A patent/US3316123A/en not_active Expired - Lifetime
Patent Citations (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2299805A (en) * | 1941-12-26 | 1942-10-27 | Detroit Gasket & Mfg Company | Packing |
| US2559234A (en) * | 1945-02-16 | 1951-07-03 | John T Stearn | Process of treating paper |
| US2482499A (en) * | 1946-05-21 | 1949-09-20 | Westinghouse Electric Corp | Laminates embodying mixed phenolarylamine-formaldehyde resinous products |
| US2536050A (en) * | 1947-11-10 | 1951-01-02 | American Cyanamid Co | Treatment of cellulosic textile materials and products thereof |
| US2537019A (en) * | 1948-05-29 | 1951-01-09 | Monsanto Chemicals | Coating compositions |
| US2708645A (en) * | 1952-04-19 | 1955-05-17 | Globe Envelopes Ltd | Method of making coated paper receptacles |
| US2787603A (en) * | 1953-07-23 | 1957-04-02 | Du Pont | Aqueous coating compositions and substrates coated therewith |
| US2772184A (en) * | 1953-09-21 | 1956-11-27 | Kimberly Clark Co | Paper coating |
| US2805621A (en) * | 1954-02-10 | 1957-09-10 | Standard Register Co | Paper planographic plate |
| US2922732A (en) * | 1955-08-12 | 1960-01-26 | Rohm & Haas | Fiber-reinforced resin-bearing tissues, films or sheets, and articles obtained therefrom |
| US2866763A (en) * | 1956-04-16 | 1958-12-30 | Du Pont | Process of preparing aqueous dispersion of an acrylonitrile interpolymer and a thermosetting resin and product obtained |
| US2889299A (en) * | 1957-07-19 | 1959-06-02 | American Cyanamid Co | Grease resistant cellulosic webs coated with a linear anionic thermoplastic ethyl acrylate-acrylonitrile-methacrylic acid polymer containing a hydrophilic inorganic pigment as extender and composition for manufacture thereof |
| US3015578A (en) * | 1958-03-25 | 1962-01-02 | American Cyanamid Co | Two-sided paper |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3442730A (en) * | 1965-09-13 | 1969-05-06 | Johns Manville | Preformed floor surface article and method of applying same |
| US3489706A (en) * | 1967-05-16 | 1970-01-13 | Goodrich Co B F | Bis(beta-chloroethyl)vinyl phosphonate copolymer compositions |
| US3676410A (en) * | 1970-08-24 | 1972-07-11 | Goodyear Tire & Rubber | Ethylhexyl acrylate-acrylonitrile-divinylbenzene terpolymers |
| US3772061A (en) * | 1971-10-14 | 1973-11-13 | Liberty Glass Co | Containers and methods of preparing |
| US3984594A (en) * | 1973-08-29 | 1976-10-05 | Kanebo, Ltd. | Method for producing cellulosic fiber-containing yarns with a non-aqueous sizing solution |
| EP4122988A1 (en) | 2021-07-23 | 2023-01-25 | Cargill, Incorporated | Water based barrier coating |
| WO2023004258A1 (en) | 2021-07-23 | 2023-01-26 | Cargill, Incorporated | Water based barrier coating |
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