US2287161A - Coated cellulosic products and method for producing the same - Google Patents
Coated cellulosic products and method for producing the same Download PDFInfo
- Publication number
- US2287161A US2287161A US315168A US31516840A US2287161A US 2287161 A US2287161 A US 2287161A US 315168 A US315168 A US 315168A US 31516840 A US31516840 A US 31516840A US 2287161 A US2287161 A US 2287161A
- Authority
- US
- United States
- Prior art keywords
- pigment
- anhydrite
- paper
- coating
- adhesive
- 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.)
- Expired - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title description 11
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 139
- 239000000049 pigment Substances 0.000 description 107
- 239000000123 paper Substances 0.000 description 67
- 229910052925 anhydrite Inorganic materials 0.000 description 62
- 239000000203 mixture Substances 0.000 description 55
- 239000002245 particle Substances 0.000 description 48
- 239000008199 coating composition Substances 0.000 description 47
- 239000000853 adhesive Substances 0.000 description 44
- 230000001070 adhesive effect Effects 0.000 description 44
- 239000000463 material Substances 0.000 description 41
- 229920002472 Starch Polymers 0.000 description 35
- 235000019698 starch Nutrition 0.000 description 35
- 238000000576 coating method Methods 0.000 description 33
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 32
- 238000010521 absorption reaction Methods 0.000 description 32
- 239000004744 fabric Substances 0.000 description 32
- 229940032147 starch Drugs 0.000 description 31
- 239000008107 starch Substances 0.000 description 31
- 239000000047 product Substances 0.000 description 27
- 239000011248 coating agent Substances 0.000 description 26
- 238000000034 method Methods 0.000 description 21
- -1 satin white Substances 0.000 description 21
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 21
- 239000002253 acid Chemical class 0.000 description 19
- 239000003513 alkali Substances 0.000 description 17
- 229920002451 polyvinyl alcohol Polymers 0.000 description 16
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 16
- 235000014633 carbohydrates Nutrition 0.000 description 15
- 150000001720 carbohydrates Chemical class 0.000 description 15
- 150000002148 esters Chemical class 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000003795 chemical substances by application Substances 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 12
- 229920003109 sodium starch glycolate Polymers 0.000 description 11
- 239000012749 thinning agent Substances 0.000 description 11
- 240000003183 Manihot esculenta Species 0.000 description 10
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 10
- 238000002156 mixing Methods 0.000 description 10
- 229940079832 sodium starch glycolate Drugs 0.000 description 10
- 239000008109 sodium starch glycolate Substances 0.000 description 10
- 239000005018 casein Substances 0.000 description 9
- 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 9
- 235000021240 caseins Nutrition 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- 229910052783 alkali metal Inorganic materials 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- 239000002002 slurry Substances 0.000 description 8
- 239000004606 Fillers/Extenders Substances 0.000 description 7
- 230000000485 pigmenting effect Effects 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 238000003490 calendering Methods 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 description 6
- 239000011707 mineral Substances 0.000 description 6
- 235000010755 mineral Nutrition 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 150000001340 alkali metals Chemical class 0.000 description 5
- 229940071117 starch glycolate Drugs 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 239000004408 titanium dioxide Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical class OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
- 150000001447 alkali salts Chemical class 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 4
- 239000011507 gypsum plaster Substances 0.000 description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 3
- 239000005083 Zinc sulfide Substances 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- ZJRXSAYFZMGQFP-UHFFFAOYSA-N barium peroxide Chemical compound [Ba+2].[O-][O-] ZJRXSAYFZMGQFP-UHFFFAOYSA-N 0.000 description 3
- 238000005282 brightening Methods 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000001747 exhibiting effect Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000005286 illumination Methods 0.000 description 3
- 229920001592 potato starch Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 229910052984 zinc sulfide Inorganic materials 0.000 description 3
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 244000151018 Maranta arundinacea Species 0.000 description 2
- 235000010804 Maranta arundinacea Nutrition 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 235000012419 Thalia geniculata Nutrition 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 125000004181 carboxyalkyl group Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 230000004313 glare Effects 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000000135 prohibitive effect Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 description 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 241000428199 Mustelinae Species 0.000 description 1
- 101150034459 Parpbp gene Proteins 0.000 description 1
- 241000274582 Pycnanthus angolensis Species 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 229920002494 Zein Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- QFFVPLLCYGOFPU-UHFFFAOYSA-N barium chromate Chemical compound [Ba+2].[O-][Cr]([O-])(=O)=O QFFVPLLCYGOFPU-UHFFFAOYSA-N 0.000 description 1
- 229940083898 barium chromate Drugs 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- ZLFVRXUOSPRRKQ-UHFFFAOYSA-N chembl2138372 Chemical compound [O-][N+](=O)C1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 ZLFVRXUOSPRRKQ-UHFFFAOYSA-N 0.000 description 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N chromium(III) oxide Inorganic materials O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- FYGDTMLNYKFZSV-MRCIVHHJSA-N dextrin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](CO)OC(O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-MRCIVHHJSA-N 0.000 description 1
- 125000006222 dimethylaminomethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])* 0.000 description 1
- VAPILSUCBNPFBS-UHFFFAOYSA-L disodium 2-oxido-5-[[4-[(4-sulfophenyl)diazenyl]phenyl]diazenyl]benzoate Chemical compound [Na+].[Na+].Oc1ccc(cc1C([O-])=O)N=Nc1ccc(cc1)N=Nc1ccc(cc1)S([O-])(=O)=O VAPILSUCBNPFBS-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 235000021463 dry cake Nutrition 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000006266 etherification reaction Methods 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
- 239000011094 fiberboard Substances 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 238000001595 flow curve Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- WOTPFVNWMLFMFW-ISLYRVAYSA-N para red Chemical compound OC1=CC=C2C=CC=CC2=C1\N=N\C1=CC=C(N(=O)=O)C=C1 WOTPFVNWMLFMFW-ISLYRVAYSA-N 0.000 description 1
- 235000020030 perry Nutrition 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 159000000005 rubidium salts Chemical class 0.000 description 1
- RCTGMCJBQGBLKT-PAMTUDGESA-N scarlet red Chemical compound CC1=CC=CC=C1\N=N\C(C=C1C)=CC=C1\N=N\C1=C(O)C=CC2=CC=CC=C12 RCTGMCJBQGBLKT-PAMTUDGESA-N 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- VVNRQZDDMYBBJY-UHFFFAOYSA-M sodium 1-[(1-sulfonaphthalen-2-yl)diazenyl]naphthalen-2-olate Chemical compound [Na+].C1=CC=CC2=C(S([O-])(=O)=O)C(N=NC3=C4C=CC=CC4=CC=C3O)=CC=C21 VVNRQZDDMYBBJY-UHFFFAOYSA-M 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 150000004897 thiazines Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910000349 titanium oxysulfate Inorganic materials 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
- 238000004018 waxing Methods 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000005019 zein Substances 0.000 description 1
- 229940093612 zein Drugs 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 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
- D21H19/44—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
- 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
- D21H19/52—Cellulose; Derivatives thereof
-
- 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
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/60—Polyalkenylalcohols; Polyalkenylethers; Polyalkenylesters
Definitions
- This invention relates to the production of improved cellulosic fabrics, and more particularly to the manufacture of coated,surfacepigmented cellulosic fabric sheets. More specifically, it relates to improved paper-coating compositions, and particularly to the production of white, coated, and surface-pigmented paper-like products. s
- Mineral materials which are usually employed in paper coating processes comprise extenders I having indices of refraction less than about 1.65,
- clay such as clay, satin white, calcium carbonate and barium sulfate, and/or various types of high strength pigments having indices' of refraction greater than about 2.0, such as titanium oxide,
- Coated paper usually has a coating in the amount of about two pounds or more of mineral material per side per 1,000 square feet of paper,
- Surface-pigmented paper usually has a coating in the amount of about one pound or less of mineral material per side per 1,000 square feet of paper. The coating'is ordinarily applied to a partially dried paper web on the paper making machine, following which the surface-pigmented paper is of coating materials. High strength pigments,
- the resultant product comprises a paper web containingpigment and adhesive. substantially entirely located in the minute surface depressions of the paper.
- Coated paper properly calendered, has a much smoother surface than uncoated paper and comprises a uniform receptor for printing ink;
- Coated paper is limited in its applications, however, because of its heavy some instances, in fact, their properties in the latter respects are even lower than those of comparable filled machine-finished papers. This is especially true-in instances of surface pigmented papers.
- said process contemplates surface-pigmenting paper or other sheeted cellulosic fabric with an oxidized elastic starch, aqueous coating composition containing as an essential ingredient thereof anhydrite of specific particle size and other definite characteristics, or a blended mixture of such anhydrite with a prime pigment, such as titanium oxide, etc.
- the calcium sulfate-containing coating compositions employed therein due to the inherent nature'of said calcium sulfate, exhibit relatively high viscosities, especially when the anhydrite and pigment content of said coating is in relatively high .or concentrated state.
- An additional object is to provide improved coating compositions adapted for use in the manufacture'of surface-pigmented, sheeted cel lulosic fabrics, such as paper.
- a further and particular object involves the provision of a useful aqueous calcium sulfate-containing coating composition of desirably non-viscous character, even when the calcium sulfate or anhydrite/pigment content thereof is in relatively high concentration.
- a specific object of the invention is to provide a process which will afford production and use of a coating composition having a relatively high anhydrite and/or prime pigment concentration and yet normally remain in satisfactory fluid or viscous condition to enable its ready application to all types of cellulosic fabrics.
- a further and particular object includes the reduction of the viscosity of aqueous adhesive cellulosic fabric coating and surface-pigmenting compositions containing calcium sulfate, and particularly anhydrite of specific particle size and other characteristics to be hereinafter set forth. Further and additional objects of the invention will become apparent from the ensuing description.
- the invention comprises incorporating in paper-coating compositions containing starch or casein and pigment-useful anhydrite, blended or unblended with a prime white pigment, relatively small amounts of a water-dispersible alkali metal salt of carboxyalkyl ethers'or acid esters of polymeric carbohydrates or polyvinyl alcohols.
- Reflectance is the ratio of light reflected from the sample to be tested to light reflected from standard fumed MgO under conditions ofequal and essentially difiused illumination and as viewed from a direction normal to the surface of the sample. Values are determined and reported corresponding to noon sunlight illumination and to the spectral region centering at 459 millimicrons, in the blue. region.
- the samples and standard are illuminated diffusely and viewed at right angles to their respective surfaces.
- the illumination is approximately completely diifused except for the viewing hole, 4 cm. in diameter, located about cm. from the sample.
- the gradings are obtained by i1- luminating the sphere wall, from which the sample is illuminated, with gas-filled incandescent lamps and viewing the sample and standard through a piece of Coming daylight glass'(melt of 1925) of suitable density for the noon sunlight grading, or a suitable blue filter for the blue region grading.
- the samples were prepared for test by pressing the dry pigment into a trough, using flne ground plate glass to form a fiat-matte surface.
- Oil-absorption is the amount of oil, in grams, required to wet 100 grams of pigment.
- Particle size refers'to the frequency particfe size average which a pigment or extender may exhibit, and may be described as the number weighted average diameter thereof.
- Consistency or apparent viscosity comprises the resistance of a material to flow at any point on a stress-flow curve.
- calcium sulfate preferably in the form of pigment-useful anhydrite and possessed of specific particle size and other characteristics, is employed in my nove1 coating composition. While use of anhydrite is preferred, other forms of calcium sulfate, such as ypsum, crown or pearl filler, etc., may also be employed, provided optimum results are not desired or essential.
- Said anhydrite desirably possesses a reflectance value in the blue region of at least about 0.9, has a frequency particle size average not exceeding about 0.7 micron, and about 90% of its particles are less than about 1.5 microns in diameter.
- Said calcium sulfate or anhydrite produces a blended pigment having an oil absorption value in the range of from about 12.5 to 37.5 when blended in the proportions of substantially 30 parts by weight of pigment titanium oxide, having an oil absorption value of about 20, with about 70 parts by weight of calcium sulfate.
- the anhydrite should have a reflectance in the'blue region of at least about 0.95, a frequency particle size average of not more than about 0.5 micron, and I at least 90% of the constituent particles thereof are less than about 1 micron in diameter; said calcium sulfate producing a blended pigment having an oil absorption value in the range of from about 25 to about 30 when blended in the proportion of about 30 parts by weight titanium oxide to 70 parts by weight calcium sulfate with a pigment titanium oxide having an oil absorption value'of 20.
- a suitable and preferred type of calcium sulfate for use in the invention is prepared by resort to special methods and procedures.
- a particularly useful and effective method comprises the following: Slaked lime containing 150 the temperature rises. relatively rapidly to approximately l20 C. and then gradually decreases. The temperature is held close to substan- .tially the boiling point during theoperation, and
- the reaction mass is maintained at such temperature, accompanied by continued and thorough agitation, until such time as the slurry becomes substantially free from acicular crystals of'gypsu'm capable of being observed under the microscope at 400 diameters magnification.
- the resultant anhydrite slurry is then filtered and washed until the filtrate shows a pH of at least about 4.
- the filter cake is then removed from Thus,
- the press repulped in fresh water, and the pH adjusted with a small amount of sodium hydroxide to about 7.5. Thereafter, the slurry is filter pressed and made ready for use, the calcium sulfate or anhydrite product being used either alone or in conjunction with a prime pigment in blended condition.
- the calcium sulfate may be suitably calcined prior to use or blending, whereby the same becomes stabilized against hydration.
- the 'anhydrite product so obtained will be of excellent white color and possess the desired reflectance, oil absorption, and particle size values referred to.
- the calcium sulfate or anhydrite may be employed in my novel coating compositions in blended or unblended condition, I preferably resort to a blend of the anhydrite with a prime pigment, such as zinc sulfide, lithopone, titanated lithopone, or titanium oxide, preferably the latter, in the proportion of about 30 parts of titanium oxide to '70 .parts of. anhydrite by weight. I preferably eflfect blending or mixing of the pigment and anhydrite, while both are in aqueous slurry, agitating the mixture for, several hours and until the individual pigment particles become completely dispersed and thoroughly blended. The resultant blended product is then filtered, dried and disintegrated, as by passage through a rotary hammer mill.
- a prime pigment such as zinc sulfide, lithopone, titanated lithopone, or titanium oxide, preferably the latter, in the proportion of about 30 parts of titanium oxide to '70 .parts of. anhydrite by weight.
- the pigment product thus obtained is then preferably mixed with water to which has been added from about 0. to about 2%, and preferably about 0.75%, on the basis of the pigment weight, of a water-dispersible alkali salt of a ,carboxyalkyl ether or acid ester of polymeric carbohydrates or polyvinyl alcohols.
- a useful and preferred water-dispersible compound comprises a sodium starch glycolate obtained by reacting modified or degraded dextrinized starch with a caustic alkali solution, and subsequently reacting the product of this reaction with sodium chloracetate under such conditions that the dextrinized starch is sufficiently depolymerized and substituted to be rendered water-soluble.
- the resultant aqueous pigment suspension is then suitably incorporated in a coating composition comprising a pigment material, an adhesive (casein, starch, glue, etc.) and water.
- a coating composition comprising a pigment material, an adhesive (casein, starch, glue, etc.) and water.
- a preferred type of composition for use in the invention may be-conveniently obtained by adding the resultant aqueous pigment suspension with stirring to an aqueous cooked starch solution comprising, say, 20% oxidized tapioca starch, whereby a coating composition consisting of, say,
- anhydrite about 10.5% anhydrite, 4.5% pigment titanium oxide, 0.11% sodium starch glycolate, and 5.25% oxidized tapioca starch, results.
- the coating composition After preparation of the coating composition, the same may be suitably applied on a paper coating machine to a cellulosic fabric or paper sheet, or directly onto the cellulosic or paper web formed on the paper machine wire.
- the resultant coated product may be suitably passed through the usual driers and then subjected to calendaring, if desired.
- a convenient, specific method for applying the coating composition comprises passing a web of paper formed on the paper machine wire through driers to reduce its moisture content to about 40 to 60%, or, if desired, to not exceeding about 6%.
- Said coating may then be applied thereto by suitably immersing the web therein, or passing said web between the nip of two squeeze rolls containing the same and spacedly disposed a definite distance from each other in a horizontal position in the same plane, said nip being kept filled by continuous addition of coating composition. Thereafter, the resultant paper product may be dried on the usual paper machine driers and calendered, if desired.
- Example I grams of a blended pigment of 25 oil absorption value, comprising 70% anhydrite (having a reflectance in the blue region of 0.96, a frequency particle size average of 0.5 micron and 95% of its particles being not greater than 1.5 microns in diameter) and 30% pigment titanium dioxide (having a reflectance in the blue region of 0.94, a frequency particle size average of 0.5 micron and 95% of its particles being not greater than 1.5 microns in diameter), was mixed accompanied by stirring with 225 grams of an aqueous solution containing 0.8 gram watersoluble sodium starch glycolate had by reacting a dextrinized tapioca starch with sodium hydroxide solution and then with sodium chloracetate.
- 70% anhydrite having a reflectance in the blue region of 0.96, a frequency particle size average of 0.5 micron and 95% of its particles being not greater than 1.5 microns in diameter
- 30% pigment titanium dioxide having a reflectance in the blue region of 0.94, a frequency particle size average of 0.5 micron and 95%
- a coating composition comprising 10.5% anhydrite, 4.5% pigment titanium dioxide, 1.12% sodium starch glycolate and 5.25% oxidized tapioca starch, resulted.
- Said coating composition had a low consistency of 7.8N, as measured on the above-described Stormer viscometer.
- Example II A similar blended pigment/oxidized tapioca starch coating composition was prepared in exactly the same manner as that of Example I, being identical in all respects, save that it contain'd no sodium starch glycolate. When similarly tested, it was determined to have a consistency value of 9.6N, which is undesirably high for certain paper and similar coating applications.
- Example III An aqueous casein paper coating composition containing 4.91% of alkali solubilized casein and 35.09% of a blended pigment comprising 30% pigment titanium dioxide and 70% anhydrite, having a reflectance in the blue region of 0.96, an oil absorption of 25, a frequency particle size average of 0.5 micron and with 90% of its par- 'identical with that of the next preceding paragraph save that 0.75% (based on the weight or the blended pigment) of a, sodium starch glycolate prepared from a dextrinized tapioca starch was added thereto, was employed.
- the resultantcomposition exhibited a much lower viscosity, giving a reading of 3.4N on the Stormer viscometer and 14.2 seconds with the Ford type viscosity cup.
- Example IV A casein coating composition similar in all respects to that of Example III hereof, but having an increased pigment content, consisting of 36.84% of the blended pigment of Example 111', 5.16% of alkali solubilized casein, and 0.28% of sodium starch glycolate, exhibited a lowerviscosity than the more dilute, untreated coating composition. Such treated composition gave viscosity readings of.4.6N on the Stormer viscometer and 15.5 seconds on the Ford type viscosity cup.
- Example 11 I have, referred to a consistency of 9.6N as rendering the coating composition nonuseful for certain paper and similar applications, it willbe understood that the specificity of the viscosity or consistency is. variable, and will largely depend upon the invinyl alcohols. Included among specificexamples of such compounds may be mentioned the ammonium, sodium, potassium or rubidium cellulose or starch glycolates; the like alkali or alkali metal saltsv of the glycolic acid ethers of polyvinyl alcohols; the ammonium, sodium, potassium or rubidium salts of the phthalic acid esters of cellulose or starch; or the like alkali or alkali metal salts of phthalic acid, esters of polyvinyl alcohols, etc.
- agents of the aforementioned class which are plaster of Paris stabilizers.
- the latter term includes all alkali polymeric polyhydroxy compounds from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols which function to prevent hydration of plaster of Pari upon being stirred in water under the relatively severe conditions to be now alluded to.
- 50 grams of plaster of Paris containing from 6.0% to 6.5% H20 by weight isadded to 200 grams of water at a temperature of 25 C. containing 0.5 gram of the agent under test.
- the resultant mixture is agitated vigorously for 1 hour by stirring in a suitable agitator or high speed mixer.
- the resulting suspension is then 1 filtered and dried to constant weightat 60 C. If, after such treatment, .the plaster of Paris contains less than 7.0% HsOby weight, the agent added to the aqueous slurry is denominated a plaster of Paris stabilizer.
- the preferred agent comprises water-soluble alkali metal cellulose or starch glycolate, particularly the latter, and the sodium starch glycolates prepared from a modified starch, such as dextrinized or degraded starch, the modified carbohydrate being readily obtained from starch by oxidationlor by hydrolysis due to' the action of dilute acids, diatase, ferments or heating. etc.
- a modified starch such as dextrinized or degraded starch
- the relatively highly water-soluble alkali metal salts of carboxy-alkyl ethers of starch or cellulose are employed, which exhibit solubility values equalling substantially that of an alkali. metal glycolate of de'xtrinized starch, such as sodium starch glycolate, or,-for example, that prepared from commercial #3 white dextrine.
- the salts of the glycolic acid ethers of starch used in my invention should preferably give solutions in which the starch granules are substantially completely broken down or dispersed.
- the salts of the glycolic acid ethers of starch which, when mixed with water give dispersions which are still principally in granular form, such as those produced from raw potato starch at a low degree of etherification, are for the purposes of this invention classed as water-insoluble.
- Specific examples of starches useful for the preparation of such starch glycolate include arrow root, tapioca, potato and corn starches previously subjected to an oxidation action with, for example,
- agent is employed in relatively minor quantity, say, as low as about 0.1% and to as high as about 2%. based on the weight of the pigment present.
- agent is employed in relatively minor quantity, say, as low as about 0.1% and to as high as about 2%. based on the weight of the pigment present.
- anhydrite which exhibits certain desired pigmentary properties, particularly in respect to particle size and other values.
- the anhydrite most preferred for use in the invention exhibits a frequency particle size average of not more than about-0.7 micron and preferably not to exceed.
- the frequency particle size average is'preferably not greater than about 0.5 micron.
- At least of the particles thereof should have diameters of less than about 1.5 microns, and preferably should have diameters of less than about 1.3 microns. For optimum benefits, 90% of said particles should have diameters of less than substantially 1 micron.
- the anhydrite should have a reflectance in the blue region of not less than about 0.9, and preferably not less than about 0.95.
- the oil absorption value of said anhydrite is determined by blendin the same with a prime pigment, preferably titanium oxide.
- the blended product when blended, for example, with titanium oxide having an oil -absorp-' tion value of 20, in the proportion of 30 parts by weight titanium oxide ,to '70 parts by weight anhydrite, the blended product should have an to about 32.5, an optimum value being in the range of from about 25 to about 30. Accordingly, the'calcium sulfate oil absorption values given herein and contemplated by the appended claims are the numerical values obtained from a blend of such pigment titanium oxide and calcium sulfate.
- While the calcium sulfate contemplated for use .in the invention may be employed as the sole pigmenting material for the coating composition, preferably, and in order to procure optimum benefits hereunder, a blended form of pigment is employed, comprising about 20 to about-40% of a prime pigment such as zinc sulfide, lithopone, titanated lithopones, and preferably titanium oxide, and from about 80 to 60% of calcium sulfate, and preferably anhydrite.
- the anhydrite and pigment may be mechanically or otherwise blended in aqueous or dry state with the prime pigment.
- a highly useful proportion consists of,
- zirconium oxide zirconium silicate, and the like
- a particularly useful blended product comprises one exhibiting an oil absorption value of the order of about 30 and preferably not less than about 21.5.
- a product of the latter type results when my special anhydrite ismixed with pigment titanium oxide having an oil absorption value of not less than substantially 20, and calcination of said anhydrite is effected at a temperature of not more than about 850 0. prior to or subsequent to blending with the prime pigment.
- the anhydrite may be mixed with the titanium oxide and calcination thereof to a temperature not exceeding about 925 C. effected prior or subsequent to blending, or said reduction in oil absorption may be effected bymilling the same in pulverizing mills such as ring roll mills, edge runner mills, pebble mills, buhrstone mills, and the like.
- a particuarly useful and efiective type of prime pigment for blending with calcium sulfate employed in the invention comprises one of requisite 693, 1,977,588, 2,006,259, and the like.
- the blended product must also' exhibit a frequency particle size average of not more than about 0.5 micron. Preferably, it exhibits a frequency particle size average of not more than about 0.4 micron, and substantially not more than about 0.3 micron. At least 90% of the particles thereof must have diameters of less than about 1.5 microns, and for optimum results 90% of the particles of the blended product should have diameters of less than about 1.3 microns, and preferably should have diameters of less than substantially 1 micron. Additionally, said blended pigment should have a reflectance value in the blue region of at least about 0.9 and preferably not less than about 0.95. Furthermore, said blended product must exhibit an oil absorption value in the range of from about '12.5 to about 37.5. Foroptimum results said oil absorption value should be in the range of from about 21.5
- aqueous slurries are entirely suitedfor blending.
- the slurries may be mixed with thorough agitation, such agitation being preferopacifyingand brightening power, particularly titanium oxide having a frequency particle sizetated'hydrous titanium oxide, as distinguished ably continued for several hours and until the individual pigment particles become completely dispersed and thoroughly blended.
- the blended mixture is then filtered, dried, and the dry cakes disintegrated.
- the adhesive composition which is preferably employed in effecting paper coating comprises an oxidized elastic starch, more specifically defined as a root or tuber starch, such as arrow root, tapioca and potato starches, and the like, previously subjected to mild oxidation,'such as by ap-' plication of barium peroxide, chlorine, sodium peroxide, etc.
- Oxidized tapioca starch comprises a preferred oxidized elastic starch in the inven- -superior results which its use induces.
- Other development through heat treatment of precipitypes of oxidized starches are also contemplated, as for example, chlorinated corn starches, etc.
- acid-treated and unmodified starches may be used in certain instances, as may casein size, and to advantage, particularly in the manufacture of coated paper or in cases where subfrom more or less colloidal or amorphous prodstantial water-resistance is desired.
- other adhesives which are soluble in aqueous media and relatively inert toward calcium sulfate, and do not react therewith to form gels, including glue, dextrin, gum arabic, gum tragacanth, or the like, may be used.
- I may employ as adhesives for the pigmenting materials various types of film-forming materials, soluble in aqueous media.
- cellulose derivatives such as methyl cellulose, glycol cellulose
- polymeric basic materials soluble in the form of their salts with acids, such as diethyl amino ethyl methacrylate, dimethyl amino ethyl methacrylate, dimethyl amino methyl zein, piper-1 larly highest opacity and brightness per unit cost and the provision of a matte surface having excellent printing properties, only result when the amount of adhesive present is less than the amount of pigment material.
- the weight of adhesive should not exceed about 60% Y of that of the pigment material. Optimum results accrue when the weight of adhesive is not greater than substantially 40% of that of the pigment material.
- a useful minimum amount comprises about of adhesive above theweight of the pigment found that the beneficial efiects thereof, particuby operation of squeeze rolls.
- said compositions may be applied by brush or roll coaters, or by any other methods well known in the art. After coating or surface-pigmenting papers with said compositions, the same may be dried in accordance with conventional procedures. After leaving the coating or squeeze rolls, the surface-pigmented papers may, for example, be passed directly to conventional paper making machine drier or to specially-constructed air tunnel driers, or a combination thereof. After leaving brush or roll coaters, the coated papers may be air or tunnel dried, as desired, or in any other manner.
- novel treating agent of my invention By use of the novel treating agent of my invention, one may utilize higher pigment concentrations in paper coating compositions, while at the same time maintaining satisfactory conditions of fluidity or viscosity in said compositions. Moreover, it permits formulation of coating compositions which are normally fluid and do not require heating prior to or during use. Furthermore, the surface-pigmented and coated cellulosic fabrics, and particularly paper, which are obtained from this iIlVGIILiOIl possess many advantages not exhibited in prior cellulosic fabric coatings.
- the surface-pigmentedpaper product obtained will exhibit unexpectedly improved opacity and brightness substantially equal to or surpassing that resulting when such papers are surface pigmented with an equal weight per unit area of a comparable aqueous coating composition containing a prime pigment alone, such as titanium oxide, as the sole pigmenting agent.
- a prime pigment alone such as titanium oxide
- the utilizable minimum of adhesive can be readily determined by trial and depends somewhat upon the oil absorption of the pigment, the type and previous history of the adhesive,' the physical characteristics .of the paper to be coated, and the use requirements of the finished paper.
- the optimum percentage of water to be employed in the coating compositions of the invention is also best determined by trial and likewise depends on the proportion of pigment material to adhesive, the oil absorption of the pigment, the
- Coating compositions comprising from about 40 to about 98% water have been advantageously employed in the invention, although optimum results accrue with compositions containing from about 50% to about 90% of water, and preferably from about 60% to about 85% of water.
- novel coating compositions of this invention may be conventionally applied to one or both sides of the paper and in any suitable manner. when employed for surface pigmentation, they may, for example, be applied by passing the paper down between the nip of coating rolls containing the coating composition, or by passing the paper through a vat containing the same, and thereafter removing the excess composition cellent printing properties and a pleasing smooth matte surface, free from objectionable high gloss
- a single application of such coating to the paper will result in a product exhibiting satisfactory opacity and brightness, whereas previously several coatings materially less concentrated in pigment would be required.
- a substantial saving in processing and elimination of undesired coating repetition results.
- the anhydrite or blends of the same with prime pigments may be mixed with other pigment materials, such as natural low-grade extenders, for example, clay and the like, or cheap precipitated extenders such as calcium carbonate, or with other pigment materials, such as barium sulfate, satin white, or the like, to produce desired and specific properties in the resultant coating composition and paper product.
- other pigment materials such as natural low-grade extenders, for example, clay and the like, or cheap precipitated extenders such as calcium carbonate, or with other pigment materials, such as barium sulfate, satin white, or the like
- no dulling or tinting agents are utilized in the coating compositions of this invention, such mateirals may be added, if desired, and in certain instances where a change in tint or increase in opacity and lower brightness of coated or surface-pigmented cellulosic fabric is sought.
- tinting and dulling materials include ultramarine blue, chrome yellow, basic zinc ch'romate, basic lead chromate, chrome orange,
- a process for producing a coated, sheeted cellulosic fabric comprising applying to said fabric an aqueous adhesive coating composition containing as an essential ingredient pigment anhydrite treated with from about .1 to 2%. based on the pigment, of a water-soluble alkali polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols as a thinning agent for said composition, said anhydrite having a reflectance value in, the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7 micron, and an oil absorption value ranging from about 12.5 to 37.5, said adhesive being relatively inert towards'said anhydrite.
- an aqueous adhesive coating composition containing as an essential ingredient pigment anhydrite treated with from about .1 to 2%. based on the pigment, of a water-soluble alkali polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and
- a process for producing a coated, sheeted cellulosic fabric comprising applying to said fabric an aqueous adhesive coating composition containing as essential ingredients a blended pigment comprising a prime pigment and calcium sulfate treated with from about .1 to 2%, based on the pigment of a water-soluble alkali polymeric polyhydroxy compound fromthe group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols as a thinning agent for said composition, said adhesive being relatively inert towards said calcium sulfate and said blended pigment having an oil absorption value in tire range of from about 12.5 to 37.5.
- a process for producing a coated, sheeted cellulosic fabric comprising applying to said fabric an aqueous adhesive coating composition containing as essential ingredients a blended titanium oxide-anhydrite pigment from about .1 to 2%, based on the pigment, of a water-soluble alkali polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols as a thinning agent for said composition, said adhesive being relatively inert towards said anhydrite and the blended pigment having an oil absorption value in the range of from about 12.5-
- a method for proving aqueous adhesive compositions employed in coating cellulosic fabrics which comprises incorporating in said composition pigment anhydrite treated with from about .1 to 2%, based on the pigment, of a watersoluble alkali metal polymeric polyhydroxy comwith a prime pigment, a reflectance value inithe blue region of not less than about 0.9, and a 2,287,161 triphenylmethane, azine and thiazine series, and
- a method for improving aqueous adhesive composition employed in coating cellulosic fabrics which comprises incorporating in said composition pigment anhydrite treated with from sheeted cellulosic fabric which comprises applying to said sheeted fabric an aqueous coating composition containing water, pigment anhydrite, and from about 0.1% to 2% of a watersoluble alkali metal polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols as a thinning agent for said composition, said anhydrite having an oil absorption value ranging from 12.5 to 37.5 upon blending with a prime pigment, and a reflectance value in the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7 micron, with 90% of the particles thereof havingdiameters of less than about 1.5 microns, the adhesive component of said composition being substantially non-reactive towards said anhydrite and present in an amount by weight not exceeding substantially of the amount of pigment material present.
- a method for producing an improved coated, sheeted cellulosic fabric which comprises applying to said fabric an aqueous coating composition containing water, a pigment material comprising a blend of from about 20- to 40 parts by weight of a prime pigment, and from about 80 to 60 parts by weight of anhydrite, from about .1 to 2%, based on the pigment, of a water-soluble, stabilizing alkali polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols as a thinning agent for said composition, an adhesive substantially non-reactive towards said anhydrite and the latter possessing an oil absorption value ranging from'12.5 to 37.5, a reflectance value in the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7 micron, and 90% of the particles of which do not exceed substantially 1.5 microns.
- anhydrite component of said composition having an oil absorption value ranging from 12.5
- a reflectance value in the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7 micron, and 90% of the particles thereof having diameters below substantially 1.5 microns.
Description
Patented June 23, 1942 UNITED" STATES? PATENT OFFICE COATED omunosrc PRODUCTS AND ME'mon ron raonucmo THE SAME Robert W. Ball, Avondale, Pa., assignor to E. I. du Pont de Nemours & Company, Wilmington, DeL, a corporation of Delaware No Drawing. Application January 23, 1940, Serial No. 315,168
16 Claims. (Cl. 106214) This invention relates to the production of improved cellulosic fabrics, and more particularly to the manufacture of coated,surfacepigmented cellulosic fabric sheets. More specifically, it relates to improved paper-coating compositions, and particularly to the production of white, coated, and surface-pigmented paper-like products. s
This application is a continuation-in-part of my co-pending application, Serial No. 258,974, filed on February 28, 1939.
Machine-finished papers produced by forming a dry, calendered web of dispersed paper fibers in which sizing material and/or fillers such as clay, titanium oxide, etc. are present or absent, exhibit many desirableproperties, particularly in respect to high bulk value, etc. Because of their relatively rough surface, these products are not adapted for use in printing. Whenever paper having a smooth surface and useful for halftone printing or the like is desired, it is cuspigmented paper, on the other hand, retains the greater bulk, lighter weight, and other advantages of machine-finished papers.
-tion, it possesses improved printing properties and desired higher brightness and opacity.
Mineral materials which are usually employed in paper coating processes comprise extenders I having indices of refraction less than about 1.65,
such as clay, satin white, calcium carbonate and barium sulfate, and/or various types of high strength pigments having indices' of refraction greater than about 2.0, such as titanium oxide,
zinc sulfide, zinc oxide, etc. Calcium sulfate has been considered undesirable for use in paper manufacture because of the objectionable char-' acteristic of this extender to lower the color or tomary to coat the base material with an aqueous composition which contains a mineral material and an adhesive such as casein, gelatine, starch, etc. Two distinct types of mineral-coated papers exist:
(1) Coated paper (2) Surface-pigmented paper Coated paper usually has a coating in the amount of about two pounds or more of mineral material per side per 1,000 square feet of paper,
applied to a previously dried web which after drying is calendered to present a paper surface substantially entirely covered with an adhesive/mineral material layer. Surface-pigmented paper usually has a coating in the amount of about one pound or less of mineral material per side per 1,000 square feet of paper. The coating'is ordinarily applied to a partially dried paper web on the paper making machine, following which the surface-pigmented paper is of coating materials. High strength pigments,
such as mentioned, produce coated, surface-pigmented papers possessing relatively high opacity and brightness. In most instances, however, their excessive cost renders use of such pigments for the purpose prohibitive. It has been proposed to employ extended forms of these pigments, utilizing such extenders as those mentimed, to obtain improved quality at practicable costs. However, paper products of unsatisfactory brightness and opacity invariably result. In
dried and calendered. The resultant product comprises a paper web containingpigment and adhesive. substantially entirely located in the minute surface depressions of the paper.
Coated paper, properly calendered, has a much smoother surface than uncoated paper and comprises a uniform receptor for printing ink;
Thus, an ordinary-grade of coated paper affords a more .faithful reproduction of the subject printed than the best grades of uncoated, supercalendered paper. Coated paper is limited in its applications, however, because of its heavy some instances, in fact, their properties in the latter respects are even lower than those of comparable filled machine-finished papers. This is especially true-in instances of surface pigmented papers.
a process which comprises coating the paper with certain types of pigments suspended in a casein size vehicle is proposed. However, surface-pigmented printing papers prepared at practicable costs, in accordance with the teachings of said patent, will be found undesirably' deficient in opacity and brightness, and also will fail to provide a matte surface having good printing qualities. Similarly, U. S. Patent weight and high c P n area. "Su fac .04 .220 Prop ses the preparatlonof coating In addi- Thus, in U. S. Patent 1,938,949 the manufacture.of white opaque waxed paper by compositions comprising titanium dioxide extended with calcium sulfate in aqueous solutions and excellent printing properties. i
It is also well known, as disclosed in U. S. Pa ents 1,682,292, 2,093,463, 2,111,272, and 2,148,951, that alkali salts of carboxyaikyl ethers or acid esters of polymeric carbohydrates or polyvinyl alcohols act as binders or fixing agents in coating compositions, or as thickening agents in textile printing. However, when employed in requisite amounts as adhesives for pigment materials, the relatively high cost of said compounds renders their use prohibitive in many instances. Furthermore, when calcium sulfate is employed in such compositions, undesirably high viscosities result, and, as a consequence a satisfactory coating medium fails to materialize in many instances.
In my concurrently-filed application, Serial No..
315,167 a process is described for producing coating compositions and the products resulting from their use, particularly surface-pigmented, sheeted cellulosic fabrics, such as surface-pigmerited paper, of excellent opacity, brightness,
and printing properties and which exhibit a relatively smooth matte surface free from objectionable gloss and glare. In its preferred embodiment, said process contemplates surface-pigmenting paper or other sheeted cellulosic fabric with an oxidized elastic starch, aqueous coating composition containing as an essential ingredient thereof anhydrite of specific particle size and other definite characteristics, or a blended mixture of such anhydrite with a prime pigment, such as titanium oxide, etc.
While a highly improved, coated or surfacepigmented product results from the process described in said co-pending application, the calcium sulfate-containing coating compositions employed therein, due to the inherent nature'of said calcium sulfate, exhibit relatively high viscosities, especially when the anhydrite and pigment content of said coating is in relatively high .or concentrated state. While to some extentthis disadvantage of high visconsity is relatively minor when relatively light-weight coatings are to be applied to a cellulosic fabric, or when coatings containing relatively minor proportions of calcium sulfate are utiiized,"difiiculty arises when application of coating compositions containing relatively large and excess concentrations of calcharacter as to be wholly unsatisfactory for producing a uniform coating on a given sheet. Accordingly, there exists a definite limit on the weight of the calcium sulfate which may be present in the coating composition. Similarly, in applying these calcium sulfate coatings to fiber board by means of press rolls, the volume of coating applied, and hence the weight thereof, is so limited that desired whitening and brightening effects cannot be obtained from application of a single coating. Furthermore, when said coating compositions are applied in large amounts, as with a brush coater, etc., drying costs markedly and objectionably increase. This for the reason that in order to obtain compositions of correct brushing viscosity, the water content thereof must be increased considerably over that of comparable prior art coating compositions.
It is among the objects of this invention to overcome these and other disadvantages in cellulosic fabric production and to provide an improved type of coated, sheeted cellulosic composition. An additional object is to provide improved coating compositions adapted for use in the manufacture'of surface-pigmented, sheeted cel lulosic fabrics, such as paper. A further and particular object involves the provision of a useful aqueous calcium sulfate-containing coating composition of desirably non-viscous character, even when the calcium sulfate or anhydrite/pigment content thereof is in relatively high concentration. A specific object of the inventionis to provide a process which will afford production and use of a coating composition having a relatively high anhydrite and/or prime pigment concentration and yet normally remain in satisfactory fluid or viscous condition to enable its ready application to all types of cellulosic fabrics. A further and particular object includes the reduction of the viscosity of aqueous adhesive cellulosic fabric coating and surface-pigmenting compositions containing calcium sulfate, and particularly anhydrite of specific particle size and other characteristics to be hereinafter set forth. Further and additional objects of the invention will become apparent from the ensuing description.
These and additional objects are attainable in my invention, which broadly comprises incorporating as an essential ingredient in cellulosic fabric coating compositions containing an adhesive and calcium sulfate (and particularly the anhydrite variety thereof) a water-dispersible alkali salt of carboxyalkyi ethers or acid esters of I polymeric carbohydrates or polyvinyl alcohols,
whereby calcium sulfate, either alone or as an extender for a prime or base pigment substance,
may be employed in such compositions in relatively high concentrations. I
In a more restricted embodiment, the invention comprises incorporating in paper-coating compositions containing starch or casein and pigment-useful anhydrite, blended or unblended with a prime white pigment, relatively small amounts of a water-dispersible alkali metal salt of carboxyalkyl ethers'or acid esters of polymeric carbohydrates or polyvinyl alcohols.
I and pigmentary characteristics, a relatively small amount of a water-soluble alkali salt of-a carboxyalkyl ether of a modified or degraded starch,
Before undertaking a more detailed description of the invention to enable its more complete understanding, an explanation of the descriptive terminology herein employed and useful methods for determining the same will now be briefly outlined.
Reflectance is the ratio of light reflected from the sample to be tested to light reflected from standard fumed MgO under conditions ofequal and essentially difiused illumination and as viewed from a direction normal to the surface of the sample. Values are determined and reported corresponding to noon sunlight illumination and to the spectral region centering at 459 millimicrons, in the blue. region.
The values of reflectance, as used herein, were measured by use of the Priest reflectometer which is essentially that described'as the Priest-Lange reflectometer in the American Enameler for August 1933, pp. 3-4.
The samples and standard are illuminated diffusely and viewed at right angles to their respective surfaces. The illumination is approximately completely diifused except for the viewing hole, 4 cm. in diameter, located about cm. from the sample. The gradings are obtained by i1- luminating the sphere wall, from which the sample is illuminated, with gas-filled incandescent lamps and viewing the sample and standard through a piece of Coming daylight glass'(melt of 1925) of suitable density for the noon sunlight grading, or a suitable blue filter for the blue region grading.
The brightness of each sample illuminated in this way was determined relative to that of magnesium oxide by a Martens photometer according to standard procedure.
The samples were prepared for test by pressing the dry pigment into a trough, using flne ground plate glass to form a fiat-matte surface.
, Oil-absorption is the amount of oil, in grams, required to wet 100 grams of pigment.
Particle size, as herein employed, refers'to the frequency particfe size average which a pigment or extender may exhibit, and may be described as the number weighted average diameter thereof.
Convenient methods for determining oil absorption and particle size values are more'particularly described in the previously issued United States patent to Hall et a1. 2,125,342, dated August 2, 1938; such described methods being the ones used for determining the oil absorption and particle size determinations employed in the instant invention.
Consistency or apparent viscosity comprises the resistance of a material to flow at any point on a stress-flow curve. The consistencies of the aqueous coating compositions herein described.
were determined on the modified Stormer viscometer, designed primarily for the determination of the. consistency of paints, which is described at page 1273, Perrys Chemical Engineers Handbook, published 1934 by McGraw-Hill Book Company, such determinations being made by the method described at pp. 1276-1277 of said book, utilizing the standard curve illustrated on page 1276.
' revolutions of spatulas.
ment, such stand being raised until the surface of the coating composition within the container rises to the mark on the spatula-like blades. Weights are applied and readings taken 'until a reading falls between 24 and 36 seconds per 100 This reading is spotted on the chart and translated into consistency by dropping vertically to the horizontal scale. The consistency determination comprises a superimposed arbitraryscale in which the numeral. 10
represents the consistency of a medium-bodied In adapting the invention to practice, calcium sulfate, preferably in the form of pigment-useful anhydrite and possessed of specific particle size and other characteristics, is employed in my nove1 coating composition. While use of anhydrite is preferred, other forms of calcium sulfate, such as ypsum, crown or pearl filler, etc., may also be employed, provided optimum results are not desired or essential. Said anhydrite desirably possesses a reflectance value in the blue region of at least about 0.9, has a frequency particle size average not exceeding about 0.7 micron, and about 90% of its particles are less than about 1.5 microns in diameter. Said calcium sulfate or anhydrite produces a blended pigment having an oil absorption value in the range of from about 12.5 to 37.5 when blended in the proportions of substantially 30 parts by weight of pigment titanium oxide, having an oil absorption value of about 20, with about 70 parts by weight of calcium sulfate. Preferably, however, the anhydrite should have a reflectance in the'blue region of at least about 0.95, a frequency particle size average of not more than about 0.5 micron, and I at least 90% of the constituent particles thereof are less than about 1 micron in diameter; said calcium sulfate producing a blended pigment having an oil absorption value in the range of from about 25 to about 30 when blended in the proportion of about 30 parts by weight titanium oxide to 70 parts by weight calcium sulfate with a pigment titanium oxide having an oil absorption value'of 20.
A suitable and preferred type of calcium sulfate for use in the invention is prepared by resort to special methods and procedures. a particularly useful and effective method comprises the following: Slaked lime containing 150 the temperature rises. relatively rapidly to approximately l20 C. and then gradually decreases. The temperature is held close to substan- .tially the boiling point during theoperation, and
the reaction mass is maintained at such temperature, accompanied by continued and thorough agitation, until such time as the slurry becomes substantially free from acicular crystals of'gypsu'm capable of being observed under the microscope at 400 diameters magnification. The resultant anhydrite slurry is then filtered and washed until the filtrate shows a pH of at least about 4. The filter cake is then removed from Thus,
the press, repulped in fresh water, and the pH adjusted with a small amount of sodium hydroxide to about 7.5. Thereafter, the slurry is filter pressed and made ready for use, the calcium sulfate or anhydrite product being used either alone or in conjunction with a prime pigment in blended condition. If desired, the calcium sulfate may be suitably calcined prior to use or blending, whereby the same becomes stabilized against hydration. The 'anhydrite product so obtained will be of excellent white color and possess the desired reflectance, oil absorption, and particle size values referred to.
While the calcium sulfate or anhydrite may be employed in my novel coating compositions in blended or unblended condition, I preferably resort to a blend of the anhydrite with a prime pigment, such as zinc sulfide, lithopone, titanated lithopone, or titanium oxide, preferably the latter, in the proportion of about 30 parts of titanium oxide to '70 .parts of. anhydrite by weight. I preferably eflfect blending or mixing of the pigment and anhydrite, while both are in aqueous slurry, agitating the mixture for, several hours and until the individual pigment particles become completely dispersed and thoroughly blended. The resultant blended product is then filtered, dried and disintegrated, as by passage through a rotary hammer mill.
The pigment product thus obtained is then preferably mixed with water to which has been added from about 0. to about 2%, and preferably about 0.75%, on the basis of the pigment weight, of a water-dispersible alkali salt of a ,carboxyalkyl ether or acid ester of polymeric carbohydrates or polyvinyl alcohols. A useful and preferred water-dispersible compound comprises a sodium starch glycolate obtained by reacting modified or degraded dextrinized starch with a caustic alkali solution, and subsequently reacting the product of this reaction with sodium chloracetate under such conditions that the dextrinized starch is sufficiently depolymerized and substituted to be rendered water-soluble. Preferably, the resultant aqueous pigment suspension is then suitably incorporated in a coating composition comprising a pigment material, an adhesive (casein, starch, glue, etc.) and water. A preferred type of composition for use in the invention may be-conveniently obtained by adding the resultant aqueous pigment suspension with stirring to an aqueous cooked starch solution comprising, say, 20% oxidized tapioca starch, whereby a coating composition consisting of, say,
about 10.5% anhydrite, 4.5% pigment titanium oxide, 0.11% sodium starch glycolate, and 5.25% oxidized tapioca starch, results. After preparation of the coating composition, the same may be suitably applied on a paper coating machine to a cellulosic fabric or paper sheet, or directly onto the cellulosic or paper web formed on the paper machine wire. The resultant coated product may be suitably passed through the usual driers and then subjected to calendaring, if desired. A convenient, specific method for applying the coating composition comprises passing a web of paper formed on the paper machine wire through driers to reduce its moisture content to about 40 to 60%, or, if desired, to not exceeding about 6%. Said coating may then be applied thereto by suitably immersing the web therein, or passing said web between the nip of two squeeze rolls containing the same and spacedly disposed a definite distance from each other in a horizontal position in the same plane, said nip being kept filled by continuous addition of coating composition. Thereafter, the resultant paper product may be dried on the usual paper machine driers and calendered, if desired.
In order that the invention may be more clearly understood, the following illustrative examples are given, which are not to be taken as in limitation of the underlying concepts of the invention:
Example I grams of a blended pigment of 25 oil absorption value, comprising 70% anhydrite (having a reflectance in the blue region of 0.96, a frequency particle size average of 0.5 micron and 95% of its particles being not greater than 1.5 microns in diameter) and 30% pigment titanium dioxide (having a reflectance in the blue region of 0.94, a frequency particle size average of 0.5 micron and 95% of its particles being not greater than 1.5 microns in diameter), was mixed accompanied by stirring with 225 grams of an aqueous solution containing 0.8 gram watersoluble sodium starch glycolate had by reacting a dextrinized tapioca starch with sodium hydroxide solution and then with sodium chloracetate. 40 grams tapioca starch,'containing 0.75% barium peroxide, was mixed with grams water, heated with stirring to about 50 C., and held at that temperature for one-half hour being stirred continuously. It was then heated with stirring to 90 C. and allowed to cool. Water was then added to said starch solution in suflicient amount to make up evaporation losses, and grams of the resultant 20% starch solution was then mixed with the aforementioned blended pig-.
ment/sodium starch glycolate/water slurry. A coating composition comprising 10.5% anhydrite, 4.5% pigment titanium dioxide, 1.12% sodium starch glycolate and 5.25% oxidized tapioca starch, resulted. Said coating composition had a low consistency of 7.8N, as measured on the above-described Stormer viscometer.
Example II A similar blended pigment/oxidized tapioca starch coating composition was prepared in exactly the same manner as that of Example I, being identical in all respects, save that it contain'd no sodium starch glycolate. When similarly tested, it was determined to have a consistency value of 9.6N, which is undesirably high for certain paper and similar coating applications.
Example III An aqueous casein paper coating composition containing 4.91% of alkali solubilized casein and 35.09% of a blended pigment comprising 30% pigment titanium dioxide and 70% anhydrite, having a reflectance in the blue region of 0.96, an oil absorption of 25, a frequency particle size average of 0.5 micron and with 90% of its par- 'identical with that of the next preceding paragraph save that 0.75% (based on the weight or the blended pigment) of a, sodium starch glycolate prepared from a dextrinized tapioca starch was added thereto, was employed. The resultantcomposition exhibited a much lower viscosity, giving a reading of 3.4N on the Stormer viscometer and 14.2 seconds with the Ford type viscosity cup.
Example IV A casein coating composition similar in all respects to that of Example III hereof, but having an increased pigment content, consisting of 36.84% of the blended pigment of Example 111', 5.16% of alkali solubilized casein, and 0.28% of sodium starch glycolate, exhibited a lowerviscosity than the more dilute, untreated coating composition. Such treated composition gave viscosity readings of.4.6N on the Stormer viscometer and 15.5 seconds on the Ford type viscosity cup.
While in Example 11 above, I have, referred to a consistency of 9.6N as rendering the coating composition nonuseful for certain paper and similar applications, it willbe understood that the specificity of the viscosity or consistency is. variable, and will largely depend upon the invinyl alcohols. Included among specificexamples of such compounds may be mentioned the ammonium, sodium, potassium or rubidium cellulose or starch glycolates; the like alkali or alkali metal saltsv of the glycolic acid ethers of polyvinyl alcohols; the ammonium, sodium, potassium or rubidium salts of the phthalic acid esters of cellulose or starch; or the like alkali or alkali metal salts of phthalic acid, esters of polyvinyl alcohols, etc.
Because of the superior results which accrue,- I prefer to employ agents of the aforementioned class which are plaster of Paris stabilizers. The latter term includes all alkali polymeric polyhydroxy compounds from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols which function to prevent hydration of plaster of Pari upon being stirred in water under the relatively severe conditions to be now alluded to. Thus, to determine whether or not such compounds are stabilizing agents, 50 grams of plaster of Paris containing from 6.0% to 6.5% H20 by weight isadded to 200 grams of water at a temperature of 25 C. containing 0.5 gram of the agent under test. The resultant mixture is agitated vigorously for 1 hour by stirring in a suitable agitator or high speed mixer. The resulting suspension is then 1 filtered and dried to constant weightat 60 C. If, after such treatment, .the plaster of Paris contains less than 7.0% HsOby weight, the agent added to the aqueous slurry is denominated a plaster of Paris stabilizer.
-,As stated, the preferred agent comprises water-soluble alkali metal cellulose or starch glycolate, particularly the latter, and the sodium starch glycolates prepared from a modified starch, such as dextrinized or degraded starch, the modified carbohydrate being readily obtained from starch by oxidationlor by hydrolysis due to' the action of dilute acids, diatase, ferments or heating. etc. Preferably, the relatively highly water-soluble alkali metal salts of carboxy-alkyl ethers of starch or cellulose are employed, which exhibit solubility values equalling substantially that of an alkali. metal glycolate of de'xtrinized starch, such as sodium starch glycolate, or,-for example, that prepared from commercial #3 white dextrine. It is to be understood that the salts of the glycolic acid ethers of starch used in my invention should preferably give solutions in which the starch granules are substantially completely broken down or dispersed. The salts of the glycolic acid ethers of starch which, when mixed with water give dispersions which are still principally in granular form, such as those produced from raw potato starch at a low degree of etherification, are for the purposes of this invention classed as water-insoluble. Specific examples of starches useful for the preparation of such starch glycolate include arrow root, tapioca, potato and corn starches previously subjected to an oxidation action with, for example,
chlorine, barium peroxide, etc. and the acid hydrolyzed starches, enzyme-treated starches, or
the like.
The optimum amount of agent utilizable in the invention is readily determined by trial, such amount being variable with the type of agent, the
type and previous history of the calcium sulfate, the proportions of the pigment material to adhesive, the type and previous history of said adhesive, the total solidscontent of the coating composition, the type of coating or surface-pig-.
menting equipment being utilized, and the use requirements of the finished, sheeted cellulosic fabric. Usually, only relatively small amounts 'of the treating agent need be employed. Thus,
when employing sodium starch glycolate, the
preferred agent, appreciable effects result when the agent is employed in relatively minor quantity, say, as low as about 0.1% and to as high as about 2%. based on the weight of the pigment present. Optimum beneficial results accrue when the amount of agent employed ranges from about 0.5% to about 1.0%, based on the Weight of the pigment material.
While various forms of calcium sulfate maybe utilized in the invention, 'to procure optimum benefits herein I preferably resort to use of anhydrite which exhibits certain desired pigmentary properties, particularly in respect to particle size and other values. Thus, the anhydrite most preferred for use in the invention exhibits a frequency particle size average of not more than about-0.7 micron and preferably not to exceed.
about 0.6 micron, whil'e said frequency particle size average is'preferably not greater than about 0.5 micron. At least of the particles thereof should have diameters of less than about 1.5 microns, and preferably should have diameters of less than about 1.3 microns. For optimum benefits, 90% of said particles should have diameters of less than substantially 1 micron. Also, the anhydrite should have a reflectance in the blue region of not less than about 0.9, and preferably not less than about 0.95. The oil absorption value of said anhydrite is determined by blendin the same with a prime pigment, preferably titanium oxide. Thus, when blended, for example, with titanium oxide having an oil -absorp-' tion value of 20, in the proportion of 30 parts by weight titanium oxide ,to '70 parts by weight anhydrite, the blended product should have an to about 32.5, an optimum value being in the range of from about 25 to about 30. Accordingly, the'calcium sulfate oil absorption values given herein and contemplated by the appended claims are the numerical values obtained from a blend of such pigment titanium oxide and calcium sulfate.
While the calcium sulfate contemplated for use .in the invention may be employed as the sole pigmenting material for the coating composition, preferably, and in order to procure optimum benefits hereunder, a blended form of pigment is employed, comprising about 20 to about-40% of a prime pigment such as zinc sulfide, lithopone, titanated lithopones, and preferably titanium oxide, and from about 80 to 60% of calcium sulfate, and preferably anhydrite. The anhydrite and pigment may be mechanically or otherwise blended in aqueous or dry state with the prime pigment. A highly useful proportion consists of,
zirconium oxide, zirconium silicate, and the like,
having a refractive index of at least about 1.8, whose pigment properties have been developed by calcination, autoclaving, or other treatment, as
' by the processes of U. S. Patents 1,704,483, 1,892,-
blending with the calcium sulfate. Whatever the of at least about 12.5, and, to insure optimum results and the provision of a matte appearance, at least about 21.5. A particularly useful blended product comprises one exhibiting an oil absorption value of the order of about 30 and preferably not less than about 21.5. m A product of the latter type results when my special anhydrite ismixed with pigment titanium oxide having an oil absorption value of not less than substantially 20, and calcination of said anhydrite is effected at a temperature of not more than about 850 0. prior to or subsequent to blending with the prime pigment. Should'a product exhibiting an oil absorption value of less than about 22.5, but not less than about 12.5, bedesired, the anhydrite may be mixed with the titanium oxide and calcination thereof to a temperature not exceeding about 925 C. effected prior or subsequent to blending, or said reduction in oil absorption may be effected bymilling the same in pulverizing mills such as ring roll mills, edge runner mills, pebble mills, buhrstone mills, and the like.
A particuarly useful and efiective type of prime pigment for blending with calcium sulfate employed in the invention comprises one of requisite 693, 1,977,588, 2,006,259, and the like.
. The blended product must also' exhibit a frequency particle size average of not more than about 0.5 micron. Preferably, it exhibits a frequency particle size average of not more than about 0.4 micron, and substantially not more than about 0.3 micron. At least 90% of the particles thereof must have diameters of less than about 1.5 microns, and for optimum results 90% of the particles of the blended product should have diameters of less than about 1.3 microns, and preferably should have diameters of less than substantially 1 micron. Additionally, said blended pigment should have a reflectance value in the blue region of at least about 0.9 and preferably not less than about 0.95. Furthermore, said blended product must exhibit an oil absorption value in the range of from about '12.5 to about 37.5. Foroptimum results said oil absorption value should be in the range of from about 21.5
' to about 32.5, and preferably should be in the drying. Such aqueous slurries are entirely suitedfor blending. The slurries may be mixed with thorough agitation, such agitation being preferopacifyingand brightening power, particularly titanium oxide having a frequency particle sizetated'hydrous titanium oxide, as distinguished ably continued for several hours and until the individual pigment particles become completely dispersed and thoroughly blended. The blended mixture is then filtered, dried, and the dry cakes disintegrated.
The adhesive composition which is preferably employed in effecting paper coating comprises an oxidized elastic starch, more specifically defined as a root or tuber starch, such as arrow root, tapioca and potato starches, and the like, previously subjected to mild oxidation,'such as by ap-' plication of barium peroxide, chlorine, sodium peroxide, etc. Oxidized tapioca starch comprises a preferred oxidized elastic starch in the inven- -superior results which its use induces. Other development through heat treatment of precipitypes of oxidized starches are also contemplated, as for example, chlorinated corn starches, etc. Also, acid-treated and unmodified starches may be used in certain instances, as may casein size, and to advantage, particularly in the manufacture of coated paper or in cases where subfrom more or less colloidal or amorphous prodstantial water-resistance is desired. Also, other adhesives which are soluble in aqueous media and relatively inert toward calcium sulfate, and do not react therewith to form gels, including glue, dextrin, gum arabic, gum tragacanth, or the like, may be used. Generally, I may employ as adhesives for the pigmenting materials various types of film-forming materials, soluble in aqueous media. These comprise (a) cellulose derivatives, such as methyl cellulose, glycol cellulose; or (b) polymeric basic materials soluble in the form of their salts with acids, such as diethyl amino ethyl methacrylate, dimethyl amino ethyl methacrylate, dimethyl amino methyl zein, piper-1 larly highest opacity and brightness per unit cost and the provision of a matte surface having excellent printing properties, only result when the amount of adhesive present is less than the amount of pigment material. Ordinarily, the weight of adhesive should not exceed about 60% Y of that of the pigment material. Optimum results accrue when the weight of adhesive is not greater than substantially 40% of that of the pigment material. While increased opacifying and brightening efiects result with even lower percentages of adhesive, too low a percentage results in coatings which dust off or become picked off during subsequent printing operations. A useful minimum amount comprises about of adhesive above theweight of the pigment found that the beneficial efiects thereof, particuby operation of squeeze rolls. When employed for paper coating, said compositions may be applied by brush or roll coaters, or by any other methods well known in the art. After coating or surface-pigmenting papers with said compositions, the same may be dried in accordance with conventional procedures. After leaving the coating or squeeze rolls, the surface-pigmented papers may, for example, be passed directly to conventional paper making machine drier or to specially-constructed air tunnel driers, or a combination thereof. After leaving brush or roll coaters, the coated papers may be air or tunnel dried, as desired, or in any other manner.
By use of the novel treating agent of my invention, one may utilize higher pigment concentrations in paper coating compositions, while at the same time maintaining satisfactory conditions of fluidity or viscosity in said compositions. Moreover, it permits formulation of coating compositions which are normally fluid and do not require heating prior to or during use. Furthermore, the surface-pigmented and coated cellulosic fabrics, and particularly paper, which are obtained from this iIlVGIILiOIl possess many advantages not exhibited in prior cellulosic fabric coatings. For example, when the calcium sulfate employed, or the blend thereof with prime pigment, has an oil absorption value in excess of about 21.5, the surface-pigmentedpaper product obtained will exhibit unexpectedly improved opacity and brightness substantially equal to or surpassing that resulting when such papers are surface pigmented with an equal weight per unit area of a comparable aqueous coating composition containing a prime pigment alone, such as titanium oxide, as the sole pigmenting agent.
. Additionally, my novel product will possess exand glare.
materialpresent. While this comprises a. preferred minimum ratio, the utilizable minimum of adhesive can be readily determined by trial and depends somewhat upon the oil absorption of the pigment, the type and previous history of the adhesive,' the physical characteristics .of the paper to be coated, and the use requirements of the finished paper.
The optimum percentage of water to be employed in the coating compositions of the invention is also best determined by trial and likewise depends on the proportion of pigment material to adhesive, the oil absorption of the pigment, the
type and previous history of the adhesive, the type of coating or surface-pigmenting equipment employed, and the use requirements of the finished paper. Coating compositions comprising from about 40 to about 98% water have been advantageously employed in the invention, although optimum results accrue with compositions containing from about 50% to about 90% of water, and preferably from about 60% to about 85% of water. a
The novel coating compositions of this invention may be conventionally applied to one or both sides of the paper and in any suitable manner. when employed for surface pigmentation, they may, for example, be applied by passing the paper down between the nip of coating rolls containing the coating composition, or by passing the paper through a vat containing the same, and thereafter removing the excess composition cellent printing properties and a pleasing smooth matte surface, free from objectionable high gloss In view of the fact that one is permitted to employ relatively high concentrations of pigmenting material in the coating composition, a single application of such coating to the paper will result in a product exhibiting satisfactory opacity and brightness, whereas previously several coatings materially less concentrated in pigment would be required. Thus, a substantial saving in processing and elimination of undesired coating repetition results.
Obviously, the anhydrite or blends of the same with prime pigments may be mixed with other pigment materials, such as natural low-grade extenders, for example, clay and the like, or cheap precipitated extenders such as calcium carbonate, or with other pigment materials, such as barium sulfate, satin white, or the like, to produce desired and specific properties in the resultant coating composition and paper product. While, preferably, no dulling or tinting agents are utilized in the coating compositions of this invention, such mateirals may be added, if desired, and in certain instances where a change in tint or increase in opacity and lower brightness of coated or surface-pigmented cellulosic fabric is sought. Examples of tinting and dulling materials include ultramarine blue, chrome yellow, basic zinc ch'romate, basic lead chromate, chrome orange,
- chrome green, barium chromate, iron blue, earth colors such as iron oxide, insoluble dyestufis such as para red and toluidine red, acid dyestufis such as pigment scarlet and lithol red, extended colors,
carbon black, tinted titanium dioxide, basic color phosphotungstates, vat dyes of the anthraquinone series, azo direct dyestuffs, basic dyes of the clude all types of paper, such as anti-tarnish bag, Bible, bond, book, catalog, coated, duplex, envelope, ledger, offset, rotog'ravure, tissue, waxing, wedding and wrapping papers, as well as bristol board, wallboard, bottle caps, boxboard,
combination board, newsboard, and patent coated board, etc,.
I claim as my invention:
1. A process for producing a coated, sheeted cellulosic fabric comprising applying to said fabric an aqueous adhesive coating composition containing as an essential ingredient pigment anhydrite treated with from about .1 to 2%. based on the pigment, of a water-soluble alkali polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols as a thinning agent for said composition, said anhydrite having a reflectance value in, the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7 micron, and an oil absorption value ranging from about 12.5 to 37.5, said adhesive being relatively inert towards'said anhydrite.
2. A process for producing a coated, sheeted cellulosic fabric. comprising applying to said fabric an aqueous adhesive coating composition containing as essential ingredients a blended pigment comprising a prime pigment and calcium sulfate treated with from about .1 to 2%, based on the pigment of a water-soluble alkali polymeric polyhydroxy compound fromthe group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols as a thinning agent for said composition, said adhesive being relatively inert towards said calcium sulfate and said blended pigment having an oil absorption value in tire range of from about 12.5 to 37.5.
3. A process for producing a coated, sheeted cellulosic fabric comprising applying to said fabric an aqueous adhesive coating composition containing as essential ingredients a blended titanium oxide-anhydrite pigment from about .1 to 2%, based on the pigment, of a water-soluble alkali polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols as a thinning agent for said composition, said adhesive being relatively inert towards said anhydrite and the blended pigment having an oil absorption value in the range of from about 12.5-
4. A method for proving aqueous adhesive compositions employed in coating cellulosic fabrics which comprises incorporating in said composition pigment anhydrite treated with from about .1 to 2%, based on the pigment, of a watersoluble alkali metal polymeric polyhydroxy comwith a prime pigment, a reflectance value inithe blue region of not less than about 0.9, and a 2,287,161 triphenylmethane, azine and thiazine series, and
frequency particle size average not exceedin about 0.7 microns, with 90% of the particles thereof having diameters of less than about 1.5 microns, and the adhesive component of said composition being substantially non-reactive towards said anhydrite.
5. A method for improving aqueous adhesive composition employed in coating cellulosic fabrics which comprises incorporating in said composition pigment anhydrite treated with from sheeted cellulosic fabric which comprises applying to said sheeted fabric an aqueous coating composition containing water, pigment anhydrite, and from about 0.1% to 2% of a watersoluble alkali metal polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols as a thinning agent for said composition, said anhydrite having an oil absorption value ranging from 12.5 to 37.5 upon blending with a prime pigment, and a reflectance value in the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7 micron, with 90% of the particles thereof havingdiameters of less than about 1.5 microns, the adhesive component of said composition being substantially non-reactive towards said anhydrite and present in an amount by weight not exceeding substantially of the amount of pigment material present.
7. A method for producing an improved coated, sheeted cellulosic fabric which comprises applying to said fabric an aqueous coating composition containing water, a pigment material comprising a blend of from about 20- to 40 parts by weight of a prime pigment, and from about 80 to 60 parts by weight of anhydrite, from about .1 to 2%, based on the pigment, of a water-soluble, stabilizing alkali polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols as a thinning agent for said composition, an adhesive substantially non-reactive towards said anhydrite and the latter possessing an oil absorption value ranging from'12.5 to 37.5, a reflectance value in the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7 micron, and 90% of the particles of which do not exceed substantially 1.5 microns.
' 8. A sheeted cellulosic fabric coated with a composition containing calcium sulfate as a pigmenting material, from about .1 to 2% of a water-soluble alkali polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols, as a thinning agent for said composition, and 'an adhesive which is substantially non-reactive towards said calcium sulfate.
9. A sheeted cellulosic fabric coated with a composition containing anhydrite as a pigmenting material, from about .1 to 2%, based on tlie pigment, of a water-soluble alkali polymeric poly- 2,287,161 hydroxy compound from the group consisting of carboxyalkyl ethers and acid, esters of carbohydrates and polyvinyl alcohols, as a thinning agent for said composition, an adhesive which is substantially non-reactive towards said anhydrite, the anhydrite component of said composi tion having an oil absorption value ranging from 12.5 to 37.5, a reflectance value in the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7 micron, and
90% of the particles thereof having diameters of less than about 1.5 microns.
10. A sheeted cellulosic fabric coated with a composition containing a blend of a prime pigment and anhydrite as a pigmenting material,
' from about .1 to 2%, based on the pigment, of
a water-soluble alkali polymeric polyhydroxy compound from the group consisting of carboxyalkyl ethers-and acid esters of carbohydrates and polyvinyl alcohols, as a thinningagent for said composition, an adhesive substantially nonreactive towards said anhydrite present in an amount by weight not exceeding substantially 60% of the amount of said pigment material,"
the anhydrite component of said composition having an oil absorption value ranging from 12.5
to 37.5, a reflectance value in the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7. micron, and 90% having diameters of less of pigment material present, saidanhydrite having an oil absorption value upon blending pigment titanium oxide with from about 80 to 60% ofanhydrite, said anhydrite in such blend ed condition having an oil absorption value ranging from 12.5 to 37.5, a reflectance value in the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7 micron,- and 90% of the particles-thereof having diameters below substantially 1.5 microns, an adhesive substantially non-reactive towards said anhydrite present in an amount by weight not exceeding substantially 60% .of the amount of pigment material present, and as a thinning agent for said composition from about 0.5 to
about 1%, on the basis of the pigment material ing from 12.5 to 37.5, a reflectance value in blue region of not less than about 0.9, a frequency particle size average .not exceeding about 0.7 micron, and 90% of the particles thereof having diameters of less than about 1.5 microns,- an adhesive substantially non-reactive towards said anhydrite present in an amount by weight not exceeding substantially 60% ofthe amountof pigment material present, and from about 0.5 to about,1%. 0n the basis of the pigment material present, of a-water-soluble alkali starch glycolate.
15. A paper product coated with an adhesive composition containing as essential ingredients a blend of from 20 to of pigment titanium oxide and from 80 to 60% of pigment anhydrite,
with a prime pigment ranging from 12.5 to 37.5, i
a reflectance value in the blue region of not less than about 0.9, a frequency particle size average not exceeding about 0.7 micron, and 90% of the particles thereof having diameters below substantially 1.5 microns.
12. A sheeted cellulosic fabric coated with an adhesive composition containing as essential inparticle size average not exceeding about 0.7
micron, and 90% of the particles thereof having diameters of less than about 1.5 microns, an adhesive substantially non-reactive towards said anhydrite present in an amount by weight not exceeding substantially 60% of the amount of pigment material present, and as a thinning agent for said composition from about 0.5 to about 1%, on the basis of the pigment material present, of a water-soluble alkali metal polymeric polyhydroxy compoundfrom the group consisting of carboxyalkyl ethers and acid esters of carbohydrates and polyvinyl alcohols.
13. A sheeted cellulosic fabric coated with an adhesive composition'containing as essential ingredients a blend-of from about20' to 40% of the anhydrite in said blend having an oil absorption value ranging from about 21.5 to 32.5, a
reflectance value in the blue region of not less than about 0.95, a frequency particle size average not exceeding about 0.6'micron and 90% of the particles thereof having diameters of less than substantially 1.3 microns, from about 0.5% to 1% of a water-soluble alkali starch glycolate as a thinning a ent, and an adhesive substantially non-reactive towards said anhydrite present in an amount by weight not exceeding substantially 60% of the amount of pigment material present in. said composition.
16. A paper product coated with an adhesive composition containing as essential ingredients .a blend of about 30 parts by weight of pigment titanium oxide to about 70 parts by weight of pigment anhydrite, from about .5% to 1% of a thinning agent for said pigment comprising a water-soluble alkali starch glycolate, an adhesive comprising an oxidized elastic starch present in. an amount by weight not exceeding substantially 40% of the amount of pigment material present, said pigment material having an oil absorption value in the range of from about 25 to 30, a reflectance value in the blue region of not less than about 0.95, a frequency particle size average not exceeding about 0.3 micron, and of the particles thereof having diameters of less than substantially 1 micron.
ROBERT w. BALL.
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US315168A US2287161A (en) | 1940-01-23 | 1940-01-23 | Coated cellulosic products and method for producing the same |
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US315168A US2287161A (en) | 1940-01-23 | 1940-01-23 | Coated cellulosic products and method for producing the same |
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US2287161A true US2287161A (en) | 1942-06-23 |
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US315168A Expired - Lifetime US2287161A (en) | 1940-01-23 | 1940-01-23 | Coated cellulosic products and method for producing the same |
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Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2419207A (en) * | 1943-09-04 | 1947-04-22 | Cons Water Power & Paper Co | Method of production of coated board and paper |
US2425058A (en) * | 1945-09-05 | 1947-08-05 | Vanderbilt Co R T | Mixtures of titanium dioxide and calcium-starch-metaborate as pigments |
US2518359A (en) * | 1947-07-21 | 1950-08-08 | United States Gypsum Co | Coating for insulation boards |
US2570499A (en) * | 1946-04-27 | 1951-10-09 | Du Pont | Starch titanium reaction product |
US2581058A (en) * | 1947-07-21 | 1952-01-01 | United States Gypsum Co | Coatings for insulation board |
US2581186A (en) * | 1948-11-18 | 1952-01-01 | Ncr Co | Paper having improved printing characteristics |
US2616818A (en) * | 1948-11-18 | 1952-11-04 | Hercules Powder Co Ltd | Paper coating |
US2661309A (en) * | 1948-11-18 | 1953-12-01 | Hercules Powder Co Ltd | Coated paper and method of producing same |
US2661308A (en) * | 1948-11-18 | 1953-12-01 | Hercules Powder Co Ltd | Process of coating paper and product resulting therefrom |
US2676118A (en) * | 1950-02-08 | 1954-04-20 | Warren S D Co | Casting support and process of manufacturing same |
US2892731A (en) * | 1954-10-08 | 1959-06-30 | Minerals & Chemicals Corp Of A | Adhesives containing kaolin |
US2993787A (en) * | 1955-08-30 | 1961-07-25 | Rca Corp | Electrostatic printing |
US3052540A (en) * | 1954-06-02 | 1962-09-04 | Rca Corp | Dye sensitization of electrophotographic materials |
US3076720A (en) * | 1957-10-25 | 1963-02-05 | Lowe Paper Co | Coated paper and polyolefin and method of coating |
US3116245A (en) * | 1958-07-23 | 1963-12-31 | Walker Mfg Co | Filter |
US3133855A (en) * | 1961-07-24 | 1964-05-19 | Kimberly Clark Co | Minimizing scratches in a blade coated paper web by roughening the smooth side of the web prior to the blade coating operation |
US3155511A (en) * | 1960-08-26 | 1964-11-03 | Andrews Paper & Chem Co Inc | Precoated diazo reproduction paper |
US3471625A (en) * | 1957-02-15 | 1969-10-07 | Harris Intertype Corp | Electrophotographic coating containing finely divided photoconductor in a synthetic polymer having ionizable functional groups |
US3510299A (en) * | 1967-06-26 | 1970-05-05 | Clifford E Herrick Jr | Method and material for the production of continuous - tone electrophotographic images |
US3839956A (en) * | 1970-07-30 | 1974-10-08 | Bell & Howell Co | Process for making dye transfer copies of improved quality |
US3865587A (en) * | 1971-07-20 | 1975-02-11 | Agfa Gevaert Nv | Electrophographic bichargeable materials and process |
US4600439A (en) * | 1982-10-12 | 1986-07-15 | Roquette Freres | Composition and process for coating paper and cardboard process for preparing the compositions and paper and cardboard so obtained |
-
1940
- 1940-01-23 US US315168A patent/US2287161A/en not_active Expired - Lifetime
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2419207A (en) * | 1943-09-04 | 1947-04-22 | Cons Water Power & Paper Co | Method of production of coated board and paper |
US2425058A (en) * | 1945-09-05 | 1947-08-05 | Vanderbilt Co R T | Mixtures of titanium dioxide and calcium-starch-metaborate as pigments |
US2570499A (en) * | 1946-04-27 | 1951-10-09 | Du Pont | Starch titanium reaction product |
US2518359A (en) * | 1947-07-21 | 1950-08-08 | United States Gypsum Co | Coating for insulation boards |
US2581058A (en) * | 1947-07-21 | 1952-01-01 | United States Gypsum Co | Coatings for insulation board |
US2581186A (en) * | 1948-11-18 | 1952-01-01 | Ncr Co | Paper having improved printing characteristics |
US2616818A (en) * | 1948-11-18 | 1952-11-04 | Hercules Powder Co Ltd | Paper coating |
US2661309A (en) * | 1948-11-18 | 1953-12-01 | Hercules Powder Co Ltd | Coated paper and method of producing same |
US2661308A (en) * | 1948-11-18 | 1953-12-01 | Hercules Powder Co Ltd | Process of coating paper and product resulting therefrom |
US2676118A (en) * | 1950-02-08 | 1954-04-20 | Warren S D Co | Casting support and process of manufacturing same |
US3052540A (en) * | 1954-06-02 | 1962-09-04 | Rca Corp | Dye sensitization of electrophotographic materials |
US2892731A (en) * | 1954-10-08 | 1959-06-30 | Minerals & Chemicals Corp Of A | Adhesives containing kaolin |
US2993787A (en) * | 1955-08-30 | 1961-07-25 | Rca Corp | Electrostatic printing |
US3471625A (en) * | 1957-02-15 | 1969-10-07 | Harris Intertype Corp | Electrophotographic coating containing finely divided photoconductor in a synthetic polymer having ionizable functional groups |
US3076720A (en) * | 1957-10-25 | 1963-02-05 | Lowe Paper Co | Coated paper and polyolefin and method of coating |
US3116245A (en) * | 1958-07-23 | 1963-12-31 | Walker Mfg Co | Filter |
US3155511A (en) * | 1960-08-26 | 1964-11-03 | Andrews Paper & Chem Co Inc | Precoated diazo reproduction paper |
US3133855A (en) * | 1961-07-24 | 1964-05-19 | Kimberly Clark Co | Minimizing scratches in a blade coated paper web by roughening the smooth side of the web prior to the blade coating operation |
US3510299A (en) * | 1967-06-26 | 1970-05-05 | Clifford E Herrick Jr | Method and material for the production of continuous - tone electrophotographic images |
US3839956A (en) * | 1970-07-30 | 1974-10-08 | Bell & Howell Co | Process for making dye transfer copies of improved quality |
US3865587A (en) * | 1971-07-20 | 1975-02-11 | Agfa Gevaert Nv | Electrophographic bichargeable materials and process |
US4600439A (en) * | 1982-10-12 | 1986-07-15 | Roquette Freres | Composition and process for coating paper and cardboard process for preparing the compositions and paper and cardboard so obtained |
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