EP1630289B1 - Coated paper product and the method for producing the same - Google Patents
Coated paper product and the method for producing the same Download PDFInfo
- Publication number
- EP1630289B1 EP1630289B1 EP05255115A EP05255115A EP1630289B1 EP 1630289 B1 EP1630289 B1 EP 1630289B1 EP 05255115 A EP05255115 A EP 05255115A EP 05255115 A EP05255115 A EP 05255115A EP 1630289 B1 EP1630289 B1 EP 1630289B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- paper product
- per
- parts
- coated paper
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 238000004519 manufacturing process Methods 0.000 title description 4
- 239000000049 pigment Substances 0.000 claims description 38
- 239000002245 particle Substances 0.000 claims description 37
- 229920002472 Starch Polymers 0.000 claims description 32
- 235000019698 starch Nutrition 0.000 claims description 30
- 238000000576 coating method Methods 0.000 claims description 22
- 239000011248 coating agent Substances 0.000 claims description 21
- 239000008199 coating composition Substances 0.000 claims description 19
- 239000008107 starch Substances 0.000 claims description 19
- 239000011800 void material Substances 0.000 claims description 19
- 239000011230 binding agent Substances 0.000 claims description 15
- 238000003490 calendering Methods 0.000 claims description 14
- 239000002023 wood Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- 108090000623 proteins and genes Proteins 0.000 claims description 8
- 102000004169 proteins and genes Human genes 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 4
- 239000001023 inorganic pigment Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 description 9
- -1 but not limited to Substances 0.000 description 7
- 230000003287 optical effect Effects 0.000 description 6
- 235000018102 proteins Nutrition 0.000 description 6
- 229920002554 vinyl polymer Polymers 0.000 description 6
- 239000004927 clay Substances 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 229920000945 Amylopectin Polymers 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 229920001897 terpolymer Polymers 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- 229920002261 Corn starch Polymers 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 239000008120 corn starch Substances 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 239000004971 Cross linker Substances 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 240000003183 Manihot esculenta Species 0.000 description 2
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 229920006317 cationic polymer Polymers 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229940100445 wheat starch Drugs 0.000 description 2
- NJVOHKFLBKQLIZ-UHFFFAOYSA-N (2-ethenylphenyl) prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1C=C NJVOHKFLBKQLIZ-UHFFFAOYSA-N 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 102000011632 Caseins Human genes 0.000 description 1
- 108010076119 Caseins Proteins 0.000 description 1
- 229920001651 Cyanoacrylate Polymers 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004716 Ethylene/acrylic acid copolymer Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 240000006394 Sorghum bicolor Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920002486 Waxy potato starch Polymers 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N acrylic acid methyl ester Natural products COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 229940021722 caseins Drugs 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 229940099112 cornstarch Drugs 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- BLCTWBJQROOONQ-UHFFFAOYSA-N ethenyl prop-2-enoate Chemical compound C=COC(=O)C=C BLCTWBJQROOONQ-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- UTVVREMVDJTZAC-UHFFFAOYSA-N furan-2-amine Chemical compound NC1=CC=CO1 UTVVREMVDJTZAC-UHFFFAOYSA-N 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 229940116317 potato starch Drugs 0.000 description 1
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229920006132 styrene block copolymer Polymers 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229940117958 vinyl acetate Drugs 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/38—Coatings with pigments characterised by the pigments
- D21H19/42—Coatings with pigments characterised by the pigments at least partly organic
-
- 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
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/10—Mixtures of chemical and mechanical pulp
-
- 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
- D21H19/50—Proteins
-
- 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
- D21H19/54—Starch
-
- 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
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/50—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by form
- D21H21/52—Additives of definite length or shape
- D21H21/54—Additives of definite length or shape being spherical, e.g. microcapsules, beads
-
- 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
- Y10T428/27—Web or sheet containing structurally defined element or component, the element or component having a specified weight per unit area [e.g., gms/sq cm, lbs/sq ft, etc.]
- Y10T428/273—Web or sheet containing structurally defined element or component, the element or component having a specified weight per unit area [e.g., gms/sq cm, lbs/sq ft, etc.] of coating
Definitions
- the present invention relates to a coated paper product that allows a coated light weight, inexpensive paper product to perform favorably when compared to a heavier coated paper product while maintaining the optical, tactile, and printing properties of the heavier coated paper product. Furthermore, this invention relates to the method for producing the same coated paper product.
- a method for preparing a coated paper product having improved properties while maintaining high bulk involves applying on a surface of a base stock at least one layer of a coating composition comprising a particulate plastic pigment; and, passing the base stock through a multi-nip calender device maintained at relatively low roll temperature and nip pressure.
- U.S. Patent No. 6,387,213 discloses a printing paper having the appearance of uncoated paper and improved printability properties approaching those of coated papers which result from the application of 7.4 to 37 gm -2 (5-25 lbs. of coating per side, per ream of paper).
- the problem addressed by the present invention is achieving good bulk and optical and printing properties while reducing the coat weight and moderating the calendering conditions in a relatively inexpensive ground-wood containing paper.
- An aspect of this invention is a coated paper product comprising:
- Another aspect of this invention is a method for producing a coated paper product comprising the steps of:
- the combination of 55 to 100 parts of voided polymeric particles per total pigment particles on a dry basis, and 10 to 50 parts of starch-based and/or protein-based binder per volume of total pigment particles on a dry basis combined with the aforementioned calender conditions enables the use of a lower coat weight; and, it enables the manufacture of lightweight and ultra light weight papers which use a greater fiber to coat ratio than is typically used in coated papers.
- Preferable coated paper product weight ranges from 35.5 to 50.3 gm -2 (24-34 lbs per ream).
- the combination of 55 to 100 part of voided polymeric particles per total pigment particles on a dry basis, and 10 to 50 parts of starch-based and/or protein-based binder per volume of total pigment particles on a dry basis combined with the aforementioned calender conditions provides for a strong paper at a given weight, which in turn provides for better runnability/ productivity on the paper machine, as well as, in subsequent printing operations than heavier counterparts. Less compression of the lighter coated paper than conventional heavier paper and retention of bulk and stiffness are some of the additional attributes achieved by using this combination. Furthermore, the optical, tactile, and printing properties of the coated paper product may be maintained at a level comparable to coated paper products having a higher initial base weight.
- gloss measured according to TAPPI 75° test procedure
- opacity measured according to TAPPI test procedure T425-OM-91
- brightness measured according to TAPPI test procedure T452-OM-92
- voided polymeric pigment particles hereinafter particles, with a particle size ranging from approximately 0.2 to 5.0 ⁇ m, preferably 0.3 to 2.0 ⁇ m and void volumes ranging from approximately 20 to 80%, preferably 40-70%.
- These particles have a density in the range of 0.4 - 1.0g/mL, preferably 0.4 - 0.6 g/mL.
- these particles include a single hollow core or void, or multiple voids within each particle; the voids may be spherical or irregular in shape and the voided areas may be isolated or connected. These particles may have an appearance of being sponge-like. The surface of these particles may range from smooth and unbroken to rough and perforated.
- Such particles are disclosed in, for example, the following patents: US 4,427,836 ; US 5,036,109 ; US 5,157,084 ; US 5,216,044 ; US 5,409,776 ; US 5,494,971 ; US 5,521,253 ; US 5,527,613 , US 5,989,630 ; US 6,020,435 ; US 6,139,961 ; and US 6,673,451 . Additionally, these particles may be cross-linked and charged; examples of cross-linked charged particles are disclosed in US 6,624,272 .
- polymeric pigment particles including but not limited to, solid polystyrene bead particles such as DOW711 and DOW722, both made by Dow Chemical Company (Midland, Mich.); solid polymethylmetlhacrylate bead particles; polymer particles with a morphology (particles comprising at least one polymer core phase containing at least one void, at least one polymer shell phase at least partially surrounding the core, and at least one channel connecting the void in the core to the exterior of the particle) and composition defined in U.S. Pat. No. 5,510,422 and European Published Patent Application No. 0 842 992 A2 ; and any polymer particles with a glass transition temperature greater than 40° C may be used in the present invention.
- solid polystyrene bead particles such as DOW711 and DOW722, both made by Dow Chemical Company (Midland, Mich.); solid polymethylmetlhacrylate bead particles; polymer particles with a morphology (particles comprising at least one poly
- mineral pigments may also be included in the present invention.
- suitable mineral pigments include but are not limited to ground and precipitated calcium carbonate, kaolin, calcined kaolin, delaminated and structured kaolin clay, titanium dioxide, aluminum silicate, magnesium silicate, magnesium carbonate, amorphous silica, zinc oxide, zinc hydroxide, aluminum oxide, aluminum hydroxide, talc, satin white, barium sulfate and calcium silicate.
- Suitable starch-based and protein-based polymeric binders of the present invention include but are not limited to, caseins, starch and wheat flours, gelatin and alginates, cellulose, hydroxyethylcellulose, methylcellulose, and carboxymethylcellulose as modified natural products, dextrins, ethylated starch (including ethylated corn starch), lignin, and the like.
- Starches which are obtainable by reacting natural, cationic, anionic and/or amphoteric starch with synthetic cationic polymers are used as dry strength agents.
- the natural starches used may be, for example, corn starch, potato starch, wheat starch, rice starch, tapioca starch, sago starch, sorghum starch, cassava starch, pea starch, rye starch or mixtures of the stated natural starches.
- Other suitable starches are ryemeal and other meals.
- Protein-containing starches from rye, wheat and leguminous plants are also suitable.
- Those natural starches which have an amylopectin content of at least 95% by weight are also suitable for the cationic modification with polymers. Starches containing at least 99% by weight of amylopectin are preferred.
- Such starches can be obtained, for example, by starch fractionation of conventional natural starches or by cultivation measures from plants which produce virtually pure amylopectin starch.
- Starches having an amylopectin content of at least 95, preferably at least 99%, by weight, are commercially available. They are offered, for example, as waxy corn starch, waxy potato starch or waxy wheat starch.
- the natural starches can be modified either alone or as a mixture with cationic polymers.
- Synthetic polymeric binders are included within the present invention from about 0 to 25 parts of synthetic binder per 100 parts of total pigment on a dry basis, preferably 5 to 25 parts of synthetic binder per 100 parts of total pigment on a dry basis.
- Suitable synthetic polymeric binders of the present invention include but are not limited to, homopolymers, copolymers or terpolymers such as acrylic and/or methacrylic polymers, polyvinyl acetate, polyvinyl alcohol, styrene-acrylic copolymers, styrene-butadiene copolymers, vinyl acetate-acrylic copolymers, ethylene-vinyl acetate copolymers, vinyl acetate-vinyl versatate copolymers, vinyl acetate-vinyl maleate copolymers, vinyl acetate-vinyl chloride-acrylic terpolymers, ethylene-vinyl acetate-acrylic terpolymers, polyurethane, polyvinyl
- the polymers or prepolymers may optionally contain up to about 10% by weight of a functional monomer, for example, but not limited to, carboxylic acid, phosphate, sulfate, sulfonate, and amide monomers and combinations thereof, non-functional monomers, and mixtures thereof.
- a functional monomer for example, but not limited to, carboxylic acid, phosphate, sulfate, sulfonate, and amide monomers and combinations thereof, non-functional monomers, and mixtures thereof.
- the polymeric binders are preferably water-borne latex polymers.
- the synthetic polymeric binders include styrene-acrylate, styrene-butadiene, styrene-butadiene-acrylonitrile, vinyl-acetate, and vinyl-acrylate.
- the coating of the present invention contains water in an amount greater than 60% of the total weight of the coating composition. Amounts of water less than 60% may achieve comparable results.
- the coating of the present invention may additionally include minor amounts, i.e., less than about 20% by weight, based on the total weight of the coating composition of conventional adhesive additives such as crosslinkers, slip agents, thickeners, bases, optical brighteners, defoamers, dispersing resins, mildewcides, biocides, opacifying pigments, extender pigments, and colorants. These optional ingredients may be added separately or added to the premixes.
- conventional adhesive additives such as crosslinkers, slip agents, thickeners, bases, optical brighteners, defoamers, dispersing resins, mildewcides, biocides, opacifying pigments, extender pigments, and colorants.
- the method of the current invention involves coating the base stock by applying the aforementioned coating with a coater and then subsequently drying the coated paper such that 1.48 to 4.4 gm -2 (1 to 3 lbs per ream) per side, preferably 1.48 to 3.7 gm -2 (1.0- 2.5 lbs per ream) per side of the dried coating composition remains on the coated paper product.
- Suitable coaters include but are not limited to short dwell, roller applicator, jet, metered size press, spray, curtain, and rod.
- the coater is a short dwell trailing blade coater having a blade of 0.457 mm/45°.
- the coater is a jet coater.
- Suitable drying methods include, but are not limited to, infrared, air-flow, and air-caps or a combination thereof.
- the coated paper is dried using IR and hot-air dryers to a moisten target of 5%.
- the coated paper is then calendered to produce the gloss and smoothness that is required for the final paper product.
- the calender intensity is lowered by reducing the number of nips, resulting in a bulkier sheet. Maintaining the number of rolls and nips while lowering the temperature and pressure has the same effect of producing a bulkier sheet.
- the coated paper web may be calendered on both sides by either two on-line soft nip calenders arranged in series or by using an offline multi-nip super-calender stack to achieve a target gloss of 50-55.
- Other suitable calenders include, but are not limited to, Jamis, Optiload, extended nip and Shoe used either on-line or off-line.
- the calendering devices of the present invention are comprised of a series of nips and rolls.
- the nips are present in quantity in a range of one to eleven.
- the rolls are present in a quantity in a range of two to twelve.
- the calendering conditions of the present invention are milder than those typically used for lightweight coated papers.
- the light weight coated paper product is calendered on both sides simultaneously by two on-line soft-nip calenders arranged in series to achieve a target gloss of 50-55.
- the soft nip calender rolls are heated to 70-200°C and a pressure load of 100-350 kN/m at each nip is applied to obtain the target gloss.
- the low weight coated paper product is calendered on an offline super-calender using at least 3 nips but no greater than 5 nips at a speed of 500m/min and a temperature from 50-150°C. No pressure is added other than the gravitational load of the rolls.
- the paper coatings were made and applied at a pilot coater facility.
- the base stock used in the examples was a ground wood containing paper with a basis weight of 35.51 gm -2 (24 lbs/3300 sq. ft.) This base stock was coated on two sides (one side at a time) using a short-dwell (blade: 0.457mm/45°) coater at a coating speed of ca. 1200 m/min (4000 ft/min) and dried using IR and hot-air dryers to a moisture target of 5%.
- Example 1 was a control coated paper product having a coating that contains no voided polymeric pigment particles per total pigment volume.
- the coating was applied to the base stock, a 10.8 kg (24 lb) ground wood-containing base stock, using a short-dwell (blade coater) at a coating speed of 1200 m/min (4000ft/min), one side at a time, such that the coat weight, as measured by an inline beta gauge, was 8.14 gm -2 /side (5.5 lbs/ream/side).
- Examples 2-7 were paper products having a coating that contains between 55 and 100 parts of voided polymeric particles per total pigment volume.
- the coating was applied, as aforementioned, to the base stock using a short-dwell (blade coater) at a coating speed of 1200 m/min (4000 ft/min), one side at a time, however, the coat weight of Examples 2-7, measured by an in-line beta gauge, was 2.96 gm -2 /side (2.0 lbs/ream/side).
Landscapes
- Paper (AREA)
Description
- The present invention relates to a coated paper product that allows a coated light weight, inexpensive paper product to perform favorably when compared to a heavier coated paper product while maintaining the optical, tactile, and printing properties of the heavier coated paper product. Furthermore, this invention relates to the method for producing the same coated paper product.
- A method for preparing a coated paper product having improved properties while maintaining high bulk, as disclosed in
U.S. Patent No. 6,531,183 , involves applying on a surface of a base stock at least one layer of a coating composition comprising a particulate plastic pigment; and, passing the base stock through a multi-nip calender device maintained at relatively low roll temperature and nip pressure. Additionally,U.S. Patent No. 6,387,213 , discloses a printing paper having the appearance of uncoated paper and improved printability properties approaching those of coated papers which result from the application of 7.4 to 37 gm-2 (5-25 lbs. of coating per side, per ream of paper). - The problem addressed by the present invention is achieving good bulk and optical and printing properties while reducing the coat weight and moderating the calendering conditions in a relatively inexpensive ground-wood containing paper.
- An aspect of this invention is a coated paper product comprising:
- a 23.7 to 53.3 gm-2 (16 to 316 lbs per ream) uncoated paper web comprising ground wood -containing pulp;
- wherein the paper web is coated on both sides with an aqueous coating composition comprising:
- 0 to 45 parts inorganic pigment per 100 parts of total pigment on a dry basis,
- 55 to 100 parts void-containing polymeric pigment particles per 100 parts of total pigment on a dry basis wherein said void containing particles have a diameter from 0.2 to 5 µm and a void volume of 20 - 80%,
- 10 to 50 parts of starch-based or protein-based polymeric binder per 100 parts of total pigment on a dry basis, wherein
- the dried and calendered coated paper product has 1.48 to 4.4 gm-2 (1 to 3 lbs per ream) per side of the dried coating composition and has a weight of 26.64 to 59.2 gm-2 (18 to 40 lbs per ream), an opacity of not greater than about 90, a gloss from 40 to 85, and a brightness from 70 to 83. As used herein, one ream is equivalent to 306.6 m2 (3300 ft2).
- Another aspect of this invention is a method for producing a coated paper product comprising the steps of:
- coating a ground wood containing paper web having an uncoated weight of 23.7 to 53.3 gm-2 (16 to 36 pounds per ream) on at least one side of the ground wood containing paper web with a coating composition comprising:
- 0 to 45 parts inorganic pigment per 100 parts of total pigment on a dry basis,
- 55 to 100 parts void-containing polymeric pigment particles per 100 parts of total pigment on a dry basis wherein said void containing particles have a diameter from 0.2 to about 5 µm and a void volume of 20 - 80%,
- 10 to 50 parts of starch-based or protein-based polymeric binder per 100 parts of total pigment on a dry basis, and water in an amount greater than 60% of the total aqueous composition,
- drying the coating composition on the paper product such
that 1.48 to 4.4 gm-2 (1 to 3 lbs per ream) per side of the dried coating composition remains on the dried coated paper product providing a dried coated paper product having a weight of 26.64 to 59.2 gm-2 (18 to 40 lbs per ream), an opacity of not greater than about 90, a gloss from 40 to 85, and a brightness from 70 to 83, and; - passing the dried coated paper product through a calender device,
wherein the calender device comprises at least two rolls and at least one nip. - The combination of 55 to 100 parts of voided polymeric particles per total pigment particles on a dry basis, and 10 to 50 parts of starch-based and/or protein-based binder per volume of total pigment particles on a dry basis combined with the aforementioned calender conditions enables the use of a lower coat weight; and, it enables the manufacture of lightweight and ultra light weight papers which use a greater fiber to coat ratio than is typically used in coated papers. Preferable coated paper product weight ranges from 35.5 to 50.3 gm-2 (24-34 lbs per ream).
- Additionally, the combination of 55 to 100 part of voided polymeric particles per total pigment particles on a dry basis, and 10 to 50 parts of starch-based and/or protein-based binder per volume of total pigment particles on a dry basis combined with the aforementioned calender conditions provides for a strong paper at a given weight, which in turn provides for better runnability/ productivity on the paper machine, as well as, in subsequent printing operations than heavier counterparts. Less compression of the lighter coated paper than conventional heavier paper and retention of bulk and stiffness are some of the additional attributes achieved by using this combination. Furthermore, the optical, tactile, and printing properties of the coated paper product may be maintained at a level comparable to coated paper products having a higher initial base weight.
- Following the application of this coating composition in the amount specified, gloss (measured according to TAPPI 75° test procedure), opacity (measured according to TAPPI test procedure T425-OM-91), and brightness (measured according to TAPPI test procedure T452-OM-92) were calculated. A coated paper product with comparable properties to a paper coated with no voided polymeric pigment and at least double the coat weight resulted. Preferable ranges for opacity and gloss are 85-90 and 50-55 respectively.
- In the coating of the present invention, there are included voided polymeric pigment particles, hereinafter particles, with a particle size ranging from approximately 0.2 to 5.0 µm, preferably 0.3 to 2.0 µm and void volumes ranging from approximately 20 to 80%, preferably 40-70%. These particles have a density in the range of 0.4 - 1.0g/mL, preferably 0.4 - 0.6 g/mL. Additionally, these particles include a single hollow core or void, or multiple voids within each particle; the voids may be spherical or irregular in shape and the voided areas may be isolated or connected. These particles may have an appearance of being sponge-like. The surface of these particles may range from smooth and unbroken to rough and perforated. Such particles are disclosed in, for example, the following patents:
US 4,427,836 ;US 5,036,109 ;US 5,157,084 ;US 5,216,044 ;US 5,409,776 ;US 5,494,971 ;US 5,521,253 ;US 5,527,613 ,US 5,989,630 ;US 6,020,435 ;US 6,139,961 ; andUS 6,673,451 . Additionally, these particles may be cross-linked and charged; examples of cross-linked charged particles are disclosed inUS 6,624,272 . - Other polymeric pigment particles, including but not limited to, solid polystyrene bead particles such as DOW711 and DOW722, both made by Dow Chemical Company (Midland, Mich.); solid polymethylmetlhacrylate bead particles; polymer particles with a morphology (particles comprising at least one polymer core phase containing at least one void, at least one polymer shell phase at least partially surrounding the core, and at least one channel connecting the void in the core to the exterior of the particle) and composition defined in
U.S. Pat. No. 5,510,422 and European Published Patent Application No.0 842 992 A2 ; and any polymer particles with a glass transition temperature greater than 40° C may be used in the present invention. - Furthermore, mineral pigments may also be included in the present invention. Suitable mineral pigments include but are not limited to ground and precipitated calcium carbonate, kaolin, calcined kaolin, delaminated and structured kaolin clay, titanium dioxide, aluminum silicate, magnesium silicate, magnesium carbonate, amorphous silica, zinc oxide, zinc hydroxide, aluminum oxide, aluminum hydroxide, talc, satin white, barium sulfate and calcium silicate.
- Suitable starch-based and protein-based polymeric binders of the present invention include but are not limited to, caseins, starch and wheat flours, gelatin and alginates, cellulose, hydroxyethylcellulose, methylcellulose, and carboxymethylcellulose as modified natural products, dextrins, ethylated starch (including ethylated corn starch), lignin, and the like. Starches which are obtainable by reacting natural, cationic, anionic and/or amphoteric starch with synthetic cationic polymers are used as dry strength agents. The natural starches used may be, for example, corn starch, potato starch, wheat starch, rice starch, tapioca starch, sago starch, sorghum starch, cassava starch, pea starch, rye starch or mixtures of the stated natural starches. Other suitable starches are ryemeal and other meals. Protein-containing starches from rye, wheat and leguminous plants are also suitable. Those natural starches which have an amylopectin content of at least 95% by weight are also suitable for the cationic modification with polymers. Starches containing at least 99% by weight of amylopectin are preferred. Such starches can be obtained, for example, by starch fractionation of conventional natural starches or by cultivation measures from plants which produce virtually pure amylopectin starch. Starches having an amylopectin content of at least 95, preferably at least 99%, by weight, are commercially available. They are offered, for example, as waxy corn starch, waxy potato starch or waxy wheat starch. The natural starches can be modified either alone or as a mixture with cationic polymers.
- Synthetic polymeric binders are included within the present invention from about 0 to 25 parts of synthetic binder per 100 parts of total pigment on a dry basis, preferably 5 to 25 parts of synthetic binder per 100 parts of total pigment on a dry basis. Suitable synthetic polymeric binders of the present invention include but are not limited to, homopolymers, copolymers or terpolymers such as acrylic and/or methacrylic polymers, polyvinyl acetate, polyvinyl alcohol, styrene-acrylic copolymers, styrene-butadiene copolymers, vinyl acetate-acrylic copolymers, ethylene-vinyl acetate copolymers, vinyl acetate-vinyl versatate copolymers, vinyl acetate-vinyl maleate copolymers, vinyl acetate-vinyl chloride-acrylic terpolymers, ethylene-vinyl acetate-acrylic terpolymers, polyurethane, polyvinyl butyral, structural acrylic polymers, anaerobic, cyanoacrylate polymers, polyvinyl chloride, polyvinylidene chloride, polyethylene, ethylene-vinyl acetate copolymers, polypropylene, ethylene/acrylic acid copolymer, ethylene/methyl acrylate copolymers, irradiated polyethylene, polyamide, polyester, epoxy, phenolic, amino, furan, polyimides, natural rubber, styrene copolymers and terpolymers, non-block, styrenic block copolymers, neoprene, nitrile rubber, butylene, polybutene, ethylene-propylene-diene rubbers, rubber silicone, and animal glue. The polymers or prepolymers may optionally contain up to about 10% by weight of a functional monomer, for example, but not limited to, carboxylic acid, phosphate, sulfate, sulfonate, and amide monomers and combinations thereof, non-functional monomers, and mixtures thereof. The polymeric binders are preferably water-borne latex polymers.
- In a preferred embodiment, the synthetic polymeric binders include styrene-acrylate, styrene-butadiene, styrene-butadiene-acrylonitrile, vinyl-acetate, and vinyl-acrylate.
- The coating of the present invention contains water in an amount greater than 60% of the total weight of the coating composition. Amounts of water less than 60% may achieve comparable results.
- The coating of the present invention may additionally include minor amounts, i.e., less than about 20% by weight, based on the total weight of the coating composition of conventional adhesive additives such as crosslinkers, slip agents, thickeners, bases, optical brighteners, defoamers, dispersing resins, mildewcides, biocides, opacifying pigments, extender pigments, and colorants. These optional ingredients may be added separately or added to the premixes.
- The method of the current invention involves coating the base stock by applying the aforementioned coating with a coater and then subsequently drying the coated paper such that 1.48 to 4.4 gm-2 (1 to 3 lbs per ream) per side, preferably 1.48 to 3.7 gm-2 (1.0- 2.5 lbs per ream) per side of the dried coating composition remains on the coated paper product. Suitable coaters include but are not limited to short dwell, roller applicator, jet, metered size press, spray, curtain, and rod. In one embodiment the coater is a short dwell trailing blade coater having a blade of 0.457 mm/45°. In another embodiment the coater is a jet coater.
- Suitable drying methods include, but are not limited to, infrared, air-flow, and air-caps or a combination thereof. In one embodiment the coated paper is dried using IR and hot-air dryers to a moisten target of 5%.
- The coated paper is then calendered to produce the gloss and smoothness that is required for the final paper product. At constant temperature and pressure the calender intensity is lowered by reducing the number of nips, resulting in a bulkier sheet. Maintaining the number of rolls and nips while lowering the temperature and pressure has the same effect of producing a bulkier sheet. The coated paper web may be calendered on both sides by either two on-line soft nip calenders arranged in series or by using an offline multi-nip super-calender stack to achieve a target gloss of 50-55. Other suitable calenders include, but are not limited to, Jamis, Optiload, extended nip and Shoe used either on-line or off-line. The calendering devices of the present invention are comprised of a series of nips and rolls. The nips are present in quantity in a range of one to eleven. The rolls are present in a quantity in a range of two to twelve. The calendering conditions of the present invention are milder than those typically used for lightweight coated papers.
- In one embodiment, the light weight coated paper product is calendered on both sides simultaneously by two on-line soft-nip calenders arranged in series to achieve a target gloss of 50-55. The soft nip calender rolls are heated to 70-200°C and a pressure load of 100-350 kN/m at each nip is applied to obtain the target gloss.
- In another embodiment, the low weight coated paper product is calendered on an offline super-calender using at least 3 nips but no greater than 5 nips at a speed of 500m/min and a temperature from 50-150°C. No pressure is added other than the gravitational load of the rolls.
- In the following examples, the paper coatings were made and applied at a pilot coater facility. The base stock used in the examples was a ground wood containing paper with a basis weight of 35.51 gm-2 (24 lbs/3300 sq. ft.) This base stock was coated on two sides (one side at a time) using a short-dwell (blade: 0.457mm/45°) coater at a coating speed of ca. 1200 m/min (4000 ft/min) and dried using IR and hot-air dryers to a moisture target of 5%.
- Example 1 was a control coated paper product having a coating that contains no voided polymeric pigment particles per total pigment volume. The coating was applied to the base stock, a 10.8 kg (24 lb) ground wood-containing base stock, using a short-dwell (blade coater) at a coating speed of 1200 m/min (4000ft/min), one side at a time, such that the coat weight, as measured by an inline beta gauge, was 8.14 gm-2 /side (5.5 lbs/ream/side). During the coating operation on the second side, half of the paper web was passed through two in-line soft-nip calender rolls, each set maintained at 170 °C with nip loads of 350 kN/m, such that a sheet gloss of about 52-53 resulted (measured by in-line gloss meter). At the end of this coating operation, the remaining coated, but uncalendered, half roll was passed through 5 nips of an off-line supercalender stack maintained at 80 °C with an applied nip load of 150 PSI to obtain sheet gloss of about 51-52 (measured by in-line gloss meter). Soft-nip calendering results are displayed within the table.
- Examples 2-7 were paper products having a coating that contains between 55 and 100 parts of voided polymeric particles per total pigment volume. The coating was applied, as aforementioned, to the base stock using a short-dwell (blade coater) at a coating speed of 1200 m/min (4000 ft/min), one side at a time, however, the coat weight of Examples 2-7, measured by an in-line beta gauge, was 2.96 gm-2/side (2.0 lbs/ream/side). During the coating operation half of the paper web was passed through two in-line soft-nip calender rolls, each set maintained at 90 °C with nip loads of 125 and 300 kN/m, such that a sheet gloss of about 50-65 was achieved (measured by in-line gloss meter). At the end of this coating operation, the remaining coated, but uncalendered, half roll passed through 3 nips of an off-line supercalender stack maintained at 60 °C with no applied nip loads (other than the gravitational weight of calender stack) to obtain a sheet gloss from about 50-65 (measured by in-line gloss meter). Soft-Nip calendering results are displayed within the table in examples 2-4, 6, and 7. Supercalendering results are displayed in Example 5.
Example→
Composition↓1 2 3 4 5 6 7 Eng. Clay (Contour 100) 87 45 # 2 Coating Clay 25 25 25 Calcined Clay (Alphatex) 10 Delam. Clay 25 TiO2 3 Hollow plastic pigment (AF-1055) 55 75 75 75 100 Hollow plastic pigment (AF-1353) 75 Starch (PG 280/270) 7 17.6 24 24 24 36 32 Synthetic Latex Binder (GenFlo® 5128) 9 12.1 16.5 16.5 16.5 16.5 22 Optical Brightner (Blancafor P) 1 1 1 1 1 Crosslinker (Sequerez 755) 0.28 0.7 0.96 0.96 0.96 1.44 1.28 Lubricant (Sunkote 455) 1 1 1 1 1 1 1 Total Target Coat Weight gm-2 16.28 5.92 5.92 5.92 5.92 5.92 5.18 (lbs/3300 sq. ft.) (11.0) (4.0) (4.0) (4.0) (4.0) (4.0) (3.5) Total Solids content (%) 58 38 33 34 34 33 29 BF Viscosity (cP) 100 rpm, 35 °C; (Spindle # 4) 1556 2400 1294 1680 1352 2516 2600 Applications data presented below is for soft-nip calendered samples (except for # 5 which was supercalendered). The opticals were measured from the rough side. Total Measured Ct. Wt. gm-2 17.46 7.4 5.92 6.22 6.96 5.92 6.01 (lbs/3300ft2) (11.8) (5.0) (4.0) (4.2) (4.7) (4.4) (4.1) 75 deg Gloss 51.5 55.2 55.6 65 48.9 50.7 55.6 Opacity 90.7 88.3 89.5 89.4 90.2 89.9 89.3 Brightness 73.1 75.8 73.7 75.2 74.8 73.1 76.8 Caliper µm 50.8 55.9 53.3 55.9 55.9 50.8 58.4 (mils) (2.0) (2.2) (2.1) (2.2) (2.2) (2.0) (2.3) Smoothness (PPS) 1.85 2.22 2.34 2.19 2.59 2.34 2.31 Sheet Porosity (mL/min) 2.1 - 3.6 4.2 4.6 2.9 -
Claims (12)
- A coated paper product comprising:a 23.7 to 53.3 gm-2 (16 to 36 lbs per ream) uncoated paper web comprising ground
wood -containing pulp;wherein the paper web is coated on both sides with an aqueous coating composition comprising:0 to 45 parts inorganic pigment per 100 parts of total pigment on a dry basis,55 to 100 parts void-containing polymeric pigment particles per 100 parts of total pigment on a dry basis wherein said void containing particles have a diameter from 0.2 to 5 µm and a void volume of 20 - 80%,10 to 50 parts of starch-based or protein-based polymeric binder per 100 parts of total pigment on a dry basis,
whereinthe dried and calendered coated paper product has 1.48 to 4.4 gm-2 (1 to 3 lbs per ream) per side of the dried coating composition and has a weight of 26.64 to 59.2 gm-2 (18 to 40 lbs per ream), an opacity of not greater than about 90, a gloss from 40 to 85, and a brightness from 70 to 83. - The coated paper product of claim 1 further comprising 5 to 25 parts of synthetic binder per 100 parts of total pigment on a dry basis.
- The coated paper product of claim 2 wherein the void-containing pigment particles comprise a particle size of 0.3-2.0 µm.
- The coated paper product of claim 3 wherein said void-containing pigment particles comprise a void volume of 40-70%.
- The coated paper product of claim 4 wherein the paper product has a weight of 35.5 to 50.3 gm-2 (24-34 lbs per ream) after coating with the composition.
- The coated paper product of claim 5 wherein the opacity is 85-90.
- The coated paper product of claim 6 wherein the gloss is 50-55.
- A method of producing a coated paper product comprising the steps ofcoating a ground wood containing paper web having an uncoated weight of 23.7 to 53.3 gm-2 (16 to 36 pounds per ream) on at least one side of the ground wood containing paper web with a coating composition comprising:0 to 45 parts inorganic pigment per 100 parts of total pigment on a dry basis,55 to 100 parts void-containing polymeric pigment particles per 100 parts of total pigment on a dry basis wherein said void containing particles have a diameter from 0.2 to about 5 µm and a void volume of 20 - 80%,10 to 50 parts of starch-based or protein-based polymeric binder per 100 parts of total pigment on a dry basis, andwater in an amount greater than 60% of the total aqueous composition,drying the coating composition on the paper product such that 1.48 to 4.4 gm-2 (1 to 3 lbs per ream) per side of the dried coating composition remains on the dried coated paper product providing a dried coated paper product having a weight of 26.64 to 59.2 gm-2 (18 to 40 lbs per ream); an opacity of not greater than about 90, a gloss from 40 to 85, and a brightness from 70 to 83, and;passing the dried coated paper product through a calender device, wherein the calender device comprises at least two rolls and at least one nip.
- The method of claim 8, wherein the coating composition is applied with a short dwell coater at a weight of 1.48 gm-2 (1.0 pound per ream) per side to 3.7 gm-2 (2.5 pounds per ream) per side, based on the total dry weight of the coating composition.
- The method of claim 8, wherein the coating composition is applied with a jet coater at a weight of 1.48 gm-2 (1.0 pound per ream) per side to 3.7 gm-2 (2.5 pounds per ream) per side, based on the total dry weight of the coating composition.
- The method of clam 8 wherein the paper product is calendered by a soft-nip calender device comprising rolls which are arranged in series wherein the device is heated to 70-200°C.
- The method of claim 8 wherein the paper product is calendered on an off-line super-calender device comprising about 3-5 nips wherein the device is heated to 50-150°C.
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EP1923504A1 (en) | 2006-11-20 | 2008-05-21 | Rohm and Haas France SAS | Coated paper and paperboard |
JP4976878B2 (en) * | 2007-02-20 | 2012-07-18 | 大王製紙株式会社 | Coated paper for printing and method for producing the same |
CN102677538B (en) * | 2007-06-18 | 2014-12-31 | 欧美诺华解决方案公司 | Paper coating compositions, coated papers, and methods |
US8382945B2 (en) | 2008-08-28 | 2013-02-26 | International Paper Company | Expandable microspheres and methods of making and using the same |
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2005
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- 2005-08-18 DE DE602005014424T patent/DE602005014424D1/en active Active
- 2005-08-18 EP EP05255115A patent/EP1630289B1/en not_active Ceased
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- 2005-08-26 CN CN200510093947.2A patent/CN100593049C/en not_active Expired - Fee Related
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CN1740441A (en) | 2006-03-01 |
JP2006063509A (en) | 2006-03-09 |
US20060042768A1 (en) | 2006-03-02 |
DE602005014424D1 (en) | 2009-06-25 |
EP1630289A1 (en) | 2006-03-01 |
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