US3808089A - Process and composition for manufacturing top liner and the like from printed and coated stock - Google Patents
Process and composition for manufacturing top liner and the like from printed and coated stock Download PDFInfo
- Publication number
- US3808089A US3808089A US17240671A US3808089A US 3808089 A US3808089 A US 3808089A US 17240671 A US17240671 A US 17240671A US 3808089 A US3808089 A US 3808089A
- Authority
- US
- United States
- Prior art keywords
- alcohol
- composition
- range
- ethylene oxide
- ethoxylated aliphatic
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Links
- 239000000203 mixture Substances 0.000 title claims abstract description 79
- 238000000034 method Methods 0.000 title claims abstract description 36
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 19
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical class C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims abstract description 41
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 38
- 229920001131 Pulp (paper) Polymers 0.000 claims abstract description 25
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims abstract description 10
- 150000004760 silicates Chemical class 0.000 claims abstract description 10
- 229910000318 alkali metal phosphate Inorganic materials 0.000 claims abstract description 9
- 150000003333 secondary alcohols Chemical class 0.000 claims description 40
- 230000002209 hydrophobic effect Effects 0.000 claims description 37
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 36
- 239000000654 additive Substances 0.000 claims description 28
- -1 aliphatic alcohols Chemical class 0.000 claims description 27
- 230000000996 additive effect Effects 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 239000003607 modifier Substances 0.000 claims description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 17
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 17
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 10
- 239000002518 antifoaming agent Substances 0.000 claims description 8
- 235000011007 phosphoric acid Nutrition 0.000 claims description 8
- 238000000926 separation method Methods 0.000 claims description 6
- 239000003381 stabilizer Substances 0.000 claims description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
- 238000013019 agitation Methods 0.000 claims description 3
- 125000005233 alkylalcohol group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000000123 paper Substances 0.000 abstract description 38
- 239000000835 fiber Substances 0.000 abstract description 16
- 238000000576 coating method Methods 0.000 abstract description 15
- 239000000463 material Substances 0.000 abstract description 14
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract description 6
- 235000000391 Lepidium draba Nutrition 0.000 abstract description 3
- 239000007844 bleaching agent Substances 0.000 abstract description 3
- 239000011087 paperboard Substances 0.000 abstract description 3
- 238000005406 washing Methods 0.000 abstract description 3
- 229920002472 Starch Polymers 0.000 abstract description 2
- 239000008107 starch Substances 0.000 abstract description 2
- 235000019698 starch Nutrition 0.000 abstract description 2
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 abstract 1
- 239000000047 product Substances 0.000 description 24
- 235000019441 ethanol Nutrition 0.000 description 21
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- 238000004513 sizing Methods 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000000470 constituent Substances 0.000 description 6
- 239000013530 defoamer Substances 0.000 description 6
- 239000002002 slurry Substances 0.000 description 6
- 238000005187 foaming Methods 0.000 description 5
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 5
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 239000004115 Sodium Silicate Substances 0.000 description 3
- 239000011149 active material Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
- 229910052911 sodium silicate Inorganic materials 0.000 description 3
- FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 3
- 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
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000003254 anti-foaming effect Effects 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
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000010893 paper waste Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000000153 supplemental effect Effects 0.000 description 2
- 238000009966 trimming Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002761 deinking Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 229910052914 metal silicate Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000011644 potassium salts of orthophosphoric acid Substances 0.000 description 1
- 235000019858 potassium salts of orthophosphoric acid Nutrition 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical class O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000011643 sodium salts of orthophosphoric acid Substances 0.000 description 1
- 235000019857 sodium salts of orthophosphoric acid Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C5/00—Other processes for obtaining cellulose, e.g. cooking cotton linters ; Processes characterised by the choice of cellulose-containing starting materials
- D21C5/02—Working-up waste paper
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/64—Paper recycling
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/02—Organic and inorganic agents containing, except water
Definitions
- ABSTRACT A method and composition for use in accordance therewith are disclosed for manufacturing top liner and other coated paper products from printed and coated paper and paperboard derived from chemical pulp with conventional paper making equipment.
- the furnish is pulped in the presence of an effective amount of ethoxylated aliphatic alcohol emulsifier in admixture with a second material selected from the group alkali metal phosphate salt and alkali metal silicate salt. No hydrogen peroxide or other bleaching agent need be present, and no extra washing or inkseparating steps are required.
- a sheet formed from the released fiber is coated, using a conventional starch coating method, to produce a white top liner or other coated paper product.
- COATING PROCESS AND COMPOSITION FOR MANUFACTURING TOP LINER AND THE LIKE FROM PRINTED AND COATED STOCK This invention generally relates to a method of utilizing cellulosic fibers released from printed and coated paper products manufactured from chemical pulp to manufacture high quality top liner and similar coated paper products.
- the present invention is also directed to a composition which can be used in practicing this method.
- Another object of the present invention is to treat printed and coated furnish derived from chemical pulp products to release the cellulosic fibers thereof and change the physical condition of the coloring and coating material contained therein to a condition wherein such fibers can be used to produce paper products which, when coated with conventional starch-clay coatings, are substantially white paper product such as, for example, top liner.
- Another object of this invention is to provide a method of manufacturing coated paper products from printed and coated furnish manufactured from chemical pulp, which method utilizes existing conventional papermaking equipment and which does not require the use of special washing steps, bleach treatment, such as, for example, with hydrogen peroxide, or the like.
- the resulting slurry is transferred to a dump chest, and subsequently passes through a conventional Jordan or refiner, stock chest, machine chest, and then to a sheet-forming machine.
- Conventional filler, sizing, color and the like can be added at the machine chest if desired.
- the sheet produced in the sheet-forming machine is coated using conventional coating methods, and the coated sheet is subsequently processed by conventional drying, finishing, trimming and the like.
- pulper is to be understood to include any equipment suitable for pulping, such as a conventional high speed pulper (Hydropulper, T.M.), likewise, as used herein, the term sheet-forming machine is intended to include conventional paper sheet-making machines such as Fourdrinier machines, cylinder machines, and the like.
- Hydropulper T.M.
- sheet-forming machine is intended to include conventional paper sheet-making machines such as Fourdrinier machines, cylinder machines, and the like.
- Emulsifier additives which are used in accordance with this invention are water-soluble emulsifiers from the group consisting of ethoxylated aliphatic alcohols.
- the modifier additives are selected from the group consisting of alkali metal phosphate salts and alkali metal silicate salts.
- the water-soluble emulsifiers referred to above are derived from substantially water-insoluble aliphatic alcohols by ethoxylation using well known techniques.
- Preferred ethoxylated aliphatic alcohols uselful in accordance with this invention are those in which the hydrophobic portions of the molecules are mixtures of straight chain alcohols.
- water-insoluble alcohols having from 5 to 20 carbons are useful as the hydrophobic moiety, and the mole ratios of combined ethylene oxide to hydrophobe can vary from 1:1 to 1:50.
- the preferred surface active compounds of this class are the alkyl polyethyleneoxy ethanols in which the starting (alkyl) alcohol is a secondary alcohol having a number of carbons in the range 11-15, and wherein the molar ratio of ethylene oxide and hydrophobic alcohol is in the range 5:1 to 15:1 with compounds having the average molar ratio in the range of 5:1 to 9:1 being most preferred.
- compositions are commercially available; for example, such compositions are available under the trade names "TERGlTOL -S-5, TERGITOL 15-S-7, TERGlTOL 15-S-9, TERGlTOL 15-S-l2,” and TERGlTOL 15-S-l5.”
- These compositions are mixtures of homologues wherein the hydrophobic alcohol is a mixture of secondary C1145 alkyl alcohols and wherein the molar ratios of ethylene oxide to hydrophobic alcohol are reportedly 5, 7, 9, 12 and 15, respectively.
- the most preferred surface active materials of this class are compounds in which the hydrophobic constituent is bonded at a secondary carbon, possibly providing a desirable degree of wettability in addition to outstanding emulsification characteristics.
- An example of a preferred emulsifier in the ethoxylated aliphatic alcohol class which is derived from a primary liner C1245 aliphatic alcohol having an ethoxy/hydrophobe molar ratio of 12:1 is NEODOL 25-12 (T.M.).
- An example of an emulsifier derived from lauryl alcohol and having an ethyleneoxy/alcohol ratio of 12:1 is LIPAL 12 LA (T.M.).
- An example of an emulsifier derived from lauryl alcohol and having an ethoxy/hydrophobe molar ratio of 8:1 is known as TRYCOL LAL-8 (T.M.).
- the emulsifier additive of this invention is added in an amount from 0.1% to 5.0% by weight based on the weight of the colored stock used.
- N is a number in the range 5-15. With the use of those commercially available materials identified by such names in which the N is the number 7, and greater numbers, the co-joint use of a defoamer is preferred.
- ethoxylated alkyl phenols such as IGEPAL CO 430, TRITON X-102," TRITON X-l 14, can be used in conjunction with the ethoxylated aliphatic alcohol type emulsifiers of this invention.
- These surface active materials have an effect on the extent of foaming and also have a highly beneficial effect on the dispersing of ink particles which are visible under 30 power magnification to such an extent that they are no longer visible under 30 power magnification.
- Preferred supplemental materials are ethoxylated alkyl phenols in which the alkyl substituent is octyl and nonyl. Alkyl phenoxy polethoxyethanols of this type are widely available surface active materials.
- the most preferred compounds of this class are those in which the alkyl substituent of the phenol group is tertiary octyl and in which the ratio of moles of ethylene oxide per mole of hydrophobe is in the range 78.
- Such most preferred materials are commercially available under the name TRITON X-l02 and TRITON X- 114.
- compounds of the ethoxylated alkyl phenol class having linear alkyl groups, such as octyl and nonyl, or in which the phenol is dialkyl substituted, are also contemplated for use as a supplemental emulsifier in accordance with this invention.
- a nonyl phenol with a 10.511 ethyle neoxy/alkyl phenol ratio is 1GB- PAL CO-710" (T.M.).
- a nbnylphenol having a 20:1 ratio of ethyleneoxy/alkyl phenol is SURPHONlC N-200 (T.M.).
- An octyl phenol-derived compound of this class having an ethyleneoxy/octyl phenol ratio of 15:1 is TRITON X- (T.M.).
- the modifier additives which are used in accordance with this invention include the sodium and potassium salts of phosphoric and silicic acid although sodium salts are preferred because of cost considerations.
- any of the fully or partially neutralized sodium and potassium salts of orthophosphoric acid are preferred metal salts for use as modifier additive, in accordance with the method of this invention.
- Aqueous solutions of alkali metal silicate salts such as sodium silicate solutions are preferred forms of the modifier additives for use in accordance with this invention.
- a formulation for practicing the above described method.
- This formulation comprises an emulsifier additive of the type generally described above, a modifier additive of the type described above, or in lieu thereof, a material which by reaction in the slurry will provide the desired alkyl metal phosphate salts and/or alkyl metal silicate salts, and a suitable stabilizer which operates to prevent separation and/or freezing of the emulsifier and modifier additives during the handling, shipping and storage thereof.
- a preferred formulation for use in the practice of the present invention which is especially suitable for use at high pH ranges (8-10) is comprised of the following:
- a suitable base such as sodium hydroxide is added with the formulation to the pulper to produce the modifier additive (e.g. phosphate salt) in situ by reaction of such base with the phosphoric acid component.
- the isopropyl alcohol component in the above formulation is used primarily to raise the cloud point to prevent separation in hot weather and to lower the freezing point in cold weather.
- Other suitable substitutes for this component will, accordingly, be apparent to those skilled in this art and would include, by way of example, only, ethyl alcohol, methyl alcohol and butyl alcohol.
- a particularly preferred embodiment of the above described formulation is composed of 60% by weight of a suitable ethoxylated aliphatic alcohol such as TER- GlTOL 15-8-5," 30% by weight of orthophosphoric acid, and by weight of isopropyl alcohol.
- water-soluble emulsifiers used in the present invention may produce foaming, it may be necessary to either incorporate a conventional antifoamer or defoamer constituent in the above formulations or, alternatively, separately add such defoamer to the pulper along with the formulation.
- Suitable antifoaming or defoamer materials will be apparent to those skilled in this art and, accordingly, a specific and detailed description thereof is not deemed necessary.
- these suitable anti-foaming or defoamer constituents would include those compositions which are currently commercially available under the trademark IGEPAL CO-430 and NETRONYX 622. These materials are used in amounts which are sufficient to control to the desired extent, or eliminate, foaming in the paper making system.
- alkali metal phosphates can be eliminated entirely and may be highly desirable in certain installations wherein it is considered beneficial to public waterway ecology to avoid phosphates.
- alkali metal silicate, or mixtures of sodium silicate and sodium hydroxide e.g. 50:50 mixtures
- the amount of modifier additive which is used is preferably the minimum amount which will provide a pH in the range 8-10, more preferably in the range 9-10.
- the scrap paper is gradually defibered and the ink is released in the aqueous phase.
- The. resulting fiber slurry-ink mixture is used in a cylinder machine process. It is noted that the slurry is not substantially diluted or cooled prior to its use in the cylinder machine.
- the resulting sheet is subsequently processed in a conventional coating method using a starch-clay coating, and the final product of the method of this invention is a white top liner of excellent quality free of waxy spots and visible ink specks.
- Example 2 The procedure of Example 1 is repeated, except that the emulsifier is added in the form of a prepared solution comprising TERGITOL l5-S-5, phosphoric acid (75%) and isopropyl alcohol in the weight ratio 60:30:10. Also, in the present example, sodium hydroxide is added instead of sodium phosphate to bring the pH to 10.0. Otherwise the conditions set forth in Example 1 are utilized and the product produced in accordance with the present example is substantially identi- 5 cal to the product produced in accordance with Example 1. It is noted that sodium phosphate is formed in situ during the pH adjustment step.
- Example 3 The procedure of Example 1 is repeated except that the emulsifier used in Example 1 is replaced by TER- GITOL 15-8-7 which was described hereinbefore, and furthermore, an effective amount of a defoamer mixture comprising IGEPAL CO-430 and NE- TRONYX 622 is used in conjunction therewith.
- Example 4 The procedure of Example 1 is repeated, except that instead of the sodium phosphate salts a 50:50 mixture of sodium hydroxide and sodium silicate is added to the aqueous system in an amount sufficient to raise the pH to 10.0. Thus, in the present example, no phosphates whatsoever are utilized. The results of the present example are substantially identical to the results achieved in the method of Example 1.
- the so-called coating method is any well-known conventional coating method for example, roll, air knife, spray coating and tub sizing.
- Tub sizing is carried out on relatively dry paper, or on surfaces which may or may not have been previously or partly sized in the beating operation.
- the material used for this treatment must have adhesive properties.
- the principal substances used for adhesive properties in tub sizing methods include animal glue, modified starches and wash sizes.
- the operation of tub sizing is carried out either on the papermaking machine itself, or in a separate sizing press employing air drying. The paper contacts size material, then runs through rolls that remove the excess material and finally runs over drying rolls. This type of sizing operation is used further to enhance the water resistance of the paper, and especially to make it take ink evenly without blurring, even after erasures.
- the formed sheet, prior to coating is in some instances lightly colored.
- any coloring remaining on the paper is so disposed that, after the coating step, the coloring is no longer visible and the product is uniformly white.
- the product of the process of this invention is free of wax specks or spots and is readily printable.
- a method for manufacturing top liner and the like from printed and coated stock derived from chemical pulp comprising the steps: agitating said stock together with an emulsifier and an additive in water to release the fibers and disperse the printing and coating constituent of said stock in said water, wherein the emulsifier is an ethoxylated aliphatic alcohol, and wherein said additive is selected from the group consisting of alkali metal phosphate salts, alkali metal silicate salts and mixtures thereof, said emulsifier being present in an effective amount in the range 0.1% to based on the weight of said stock, said additive being present in an amount from 0.0125% to 6.25% based on the weight of said stock, and said dispersing of said stock being conducted at an alkaline pH, said dispersing step resulting in the formation of a slurry wherein said stock as well as the printing and coating constituents thereof are dispersed; charging said slurry to a sheet forming machine and forming a paper sheet from the resulting released fibers;
- ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 1 115 carbons, and wherein the average molar ratio of etylene oxide to hydrophobic alcohol is in the range 5:1 to :1.
- ethoxylated aliphatic alcohol is one in which the hydrophobic portion is a mixture of straight chain aliphatic alcohols and the average mole ratio of the combined ethylene oxide to hydrophobic portion is in the range 1-50.
- the emulsifier is an alkyl polyethyleneoxy ethanol in which the alkyl portion is derived from a secondary alcohol having 1 1-15 carbons and wherein the average molar ratio of combined ethylene oxide and secondary alcohol is in the range 5:1 to 9:1.
- the emulsifier is derived from a water-insoluble secondary alcohol having a number of carbons in the range 11-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1, and in which an anti-foaming agent is also present during the agitation.
- a composition for use in the manufacture of top liner and the like from printed and coated stock derived from chemical pulp consisting essentially of from 40% to 80% by weight of an ethoxylated aliphatic alcohol, from 10% to 50% by weight of a modifier additive selected from the class consisting of alkali metal phosphate salts, alkali metal silicate salts and mixtures thereof, and from 5% to by weight of a stabilizer which prevents separation of said ethoxylated aliphatic alcohol and said modifier additive during the shipping and handling of said composition.
- composition of claim 6 wherein said stabilizer is an alkyl alcohol having from 1 to 4 carbon atoms.
- composition of claim 6 wherein said modifier additive is orthophosphoric acid.
- composition of claim 6 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 1 1-15 carbons, and wherein the average molar ratio of ethylene oxide to hydrophobic alcohol is in the range 5:1 to 15:1.
- composition of claim 6 wherein the ethoxylated aliphatic alcohol is one in which the hydrophobic portion is a mixture of straight chain aliphatic alcohols and the average mole ratio of the combined ethylene oxide to hydrophobic portion is in the range 1-50.
- composition of claim 6 in which said ethoxylated aliphatic alcohol is an alkyl polyethyleneoxy ethanol in which the alkyl portion is derived from a secondary alcohol having 1 l-15 carbons and wherein the average molar ratio of combined ethylene oxide and secondary alcohol is in the range 5:1 to 9:1.
- composition of claim 6 in which said ethoxylated aliphatic alcohol is derived from a water-insoluble secondary alcohol having a number of carbons in the range 11-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1 and in which an anti-foaming agent is also present.
- composition of claim 13 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 1 1-15 carbons, and wherein the average molar ratio of ethylene oxide to hydrophobic alcohol is in the range 5:1 to 15:1.
- composition of claim 13 wherein the ethoxylated aliphatic alcohol is one in which the hydrophobic portion is a mixture of straight chain aliphatic alcohols and the average mole ratio of the combined ethylene oxide to hydrophobic portion is in the range l50.
- composition of claim 13 in which said ethoxylated aliphatic alcohol is an alkyl polyethyleneoxy ethanol in which the alkyl portion is derived from a secondary alcohol having 1 l-l 5 carbons and wherein the average molar ratio of combined ethylene oxide and secondary alcohol is in the range 5:1 to 9:1.
- composition of claim 13 in which said ethoxylated aliphatic alcohol is derived from a waterinsoluble secondary alcohol having a number of carbons in the range ll-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1 and in which an anti-foaming agent is also present.
- composition of claim 18 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 11-15 carbons, and wherein the average molar ratio of ethylene oxide to hydrophobic alcohol is in the range 5:1 to 15:1.
- ondary alcohol is in the range 5:1 to 9:1.
- composition of claim 18 in which said ethoxylated aliphatic alcohol is derived from a waterinsoluble secondary alcohol having a number of carbons in the range 11-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1 and in which an anti-foaming agent is also present.
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Abstract
A method and composition for use in accordance therewith are disclosed for manufacturing top liner and other coated paper products from printed and coated paper and paperboard derived from chemical pulp with conventional paper making equipment. The furnish is pulped in the presence of an effective amount of ethoxylated aliphatic alcohol emulsifier in admixture with a second material selected from the group alkali metal phosphate salt and alkali metal silicate salt. No hydrogen peroxide or other bleaching agent need be present, and no extra washing or ink-separating steps are required. A sheet formed from the released fiber is coated, using a conventional starch coating method, to produce a white top liner or other coated paper product.
Description
United States Patent Von Koeppen et al.
[ Apr. 30, 1974 [75] Inventors: Andreas Von Koeppen, Lombard;
Reinaldo T. Carrera, Chicago, both of I11.
[73] Assignee: Wright Chemical Corporation, Chicago, Ill.
22 Filed: Aug. 17, 1971 211 App]. No.: 172,406
[52] US. Cl 162/5, 252/136, 252/139,
252/352, 252/DIG. 1
[51] Int. Cl. D21c 5/02 [58] Field of Search 162/5, 72, 77, 4; 252/351, 252/352, 357, 139, 136, DIG. 1
Stephenson, J. Newell; Pulp and Paper Manufacture; Vol. 2 and 3, McGraw-Hill Book Co., N.Y., N.Y., 1951, v01. 2 page 148, V0] 3, 758-759.
Primary Examiner-S. Leon Bashore Assistant Examiner-William F. Smith Attorney, Agent, or Firm-Lockwood, Dewey, Zickert & Alex [57] ABSTRACT A method and composition for use in accordance therewith are disclosed for manufacturing top liner and other coated paper products from printed and coated paper and paperboard derived from chemical pulp with conventional paper making equipment. The furnish is pulped in the presence of an effective amount of ethoxylated aliphatic alcohol emulsifier in admixture with a second material selected from the group alkali metal phosphate salt and alkali metal silicate salt. No hydrogen peroxide or other bleaching agent need be present, and no extra washing or inkseparating steps are required. A sheet formed from the released fiber is coated, using a conventional starch coating method, to produce a white top liner or other coated paper product.
22 Claims, 1 Drawing Figure MODIFIER PAPER-FIBER souRcE I ADDITIVE PRINTED WASTE PAPER L l I DERIVED FROM PULPER H WATER I l .CHEM'CAL PULP EMULSIFIER I ADDITIVE DUMP CHEST I FILLER, SIZING, l "JORDAN" 0R "REFINER" COLOR wATER l FJ, I STOCK CHEST, SHEET DRYING, SALABLE MACHINE CHEST FORMING FINISHING, PRODUCT TRIMMING, ETc.
COATING PROCESS AND COMPOSITION FOR MANUFACTURING TOP LINER AND THE LIKE FROM PRINTED AND COATED STOCK This invention generally relates to a method of utilizing cellulosic fibers released from printed and coated paper products manufactured from chemical pulp to manufacture high quality top liner and similar coated paper products. The present invention is also directed to a composition which can be used in practicing this method.
In conventional paper and paperboard manufacture, there are at least four different kinds of wood pulp which are commonly identified as mechanical pulp, sulfite pulp, sulfate pulp and soda pulp. While mechanical pulp is prepared by purely mechanical means, sulfite, sulfate and soda pulps are prepared by chemical means. Mechanical pulp contains all of the wood constituents except the bark and that which is lost during storage and transportation. Chemical pulps are essentially pure cellulose having been freed of unwanted lignin and other non-cellulosic components of the wood which are dissolved away by the chemical pulp treatment. Chemical pulps, accordingly, are much superior in quality to mechanical pulp for fine paper making. As a result of the special processing required, however, chemical pulps are considered too expensive for the cheaper grades of paper, such as newsprint. The relatively high cost of chemical pulp paper products makes it highly desirable to provide a process whereby waste from such products, even though printed and colored, can be used as a source for cellulosic fiber in the manufacture of paper products, particularly high quality paper products such as, for example, top liner and similar coated paper products.
While numerous methods of de-inking paper products have been suggested heretofore, these methods have generally involved the steps of either the separation of ink from the slurry containing the fiber or the bleaching of released fibers to eliminate the ink color from the fiber-containing system. More specifically, these prior art deinking processes have generally contempated as an essential thereto, the elimination of ink particles prior to sheet formation by conventional liquid-solid separation techniques such as, for example, skimming, flotation and filtration, or either conjointly or in the alternative, bleaching of the released fibers.
It is an object of this invention to provide an improved method and composition for recovering cellulosic fibers from printed and coated chemical pulp products, and for manufacturing coated paper products therewith such as, for example, top liner and the like.
Another object of the present invention is to treat printed and coated furnish derived from chemical pulp products to release the cellulosic fibers thereof and change the physical condition of the coloring and coating material contained therein to a condition wherein such fibers can be used to produce paper products which, when coated with conventional starch-clay coatings, are substantially white paper product such as, for example, top liner.
Another object of this invention is to provide a method of manufacturing coated paper products from printed and coated furnish manufactured from chemical pulp, which method utilizes existing conventional papermaking equipment and which does not require the use of special washing steps, bleach treatment, such as, for example, with hydrogen peroxide, or the like.
These and other objects which will be apparent hereinafter are all achieved in accordance with the method of this invention which is described in general, and in connection with particularly preferred embodiments hereinafter, with the aid of the accompanying drawing which is a schematic flow sheet of a paper making system wherein the process of the present invention may be employed.
The process described on the flow sheet generally includes steps well known and widely used in the art of manufacturing paper products such as top liner and the like and which, therefore, need not be extensively discussed herein. In accordance with an important aspect of this invention, however, printed waste paper derived from chemical pulp such as, for example, dixie cups, milk cartons, magazines, and the like is charged to a conventional pulper, along with water, a special emulsifier additive and a modifier additive. Agitation in the pulper is, in some embodiments, preferably carried out with the contents of the pulper at an elevated temperature, such as, for example, about F. After the cellulosic fibers are released, the resulting slurry is transferred to a dump chest, and subsequently passes through a conventional Jordan or refiner, stock chest, machine chest, and then to a sheet-forming machine. Conventional filler, sizing, color and the like can be added at the machine chest if desired. In accordance with the present invention, the sheet produced in the sheet-forming machine is coated using conventional coating methods, and the coated sheet is subsequently processed by conventional drying, finishing, trimming and the like.
The term pulper, as used herein, is to be understood to include any equipment suitable for pulping, such as a conventional high speed pulper (Hydropulper, T.M.), likewise, as used herein, the term sheet-forming machine is intended to include conventional paper sheet-making machines such as Fourdrinier machines, cylinder machines, and the like.
Emulsifier additives which are used in accordance with this invention are water-soluble emulsifiers from the group consisting of ethoxylated aliphatic alcohols. The modifier additives are selected from the group consisting of alkali metal phosphate salts and alkali metal silicate salts.
The water-soluble emulsifiers referred to above are derived from substantially water-insoluble aliphatic alcohols by ethoxylation using well known techniques. Preferred ethoxylated aliphatic alcohols uselful in accordance with this invention are those in which the hydrophobic portions of the molecules are mixtures of straight chain alcohols. For example, water-insoluble alcohols having from 5 to 20 carbons are useful as the hydrophobic moiety, and the mole ratios of combined ethylene oxide to hydrophobe can vary from 1:1 to 1:50. The preferred surface active compounds of this class are the alkyl polyethyleneoxy ethanols in which the starting (alkyl) alcohol is a secondary alcohol having a number of carbons in the range 11-15, and wherein the molar ratio of ethylene oxide and hydrophobic alcohol is in the range 5:1 to 15:1 with compounds having the average molar ratio in the range of 5:1 to 9:1 being most preferred. A number of such compositions are commercially available; for example, such compositions are available under the trade names "TERGlTOL -S-5, TERGITOL 15-S-7, TERGlTOL 15-S-9, TERGlTOL 15-S-l2," and TERGlTOL 15-S-l5." These compositions are mixtures of homologues wherein the hydrophobic alcohol is a mixture of secondary C1145 alkyl alcohols and wherein the molar ratios of ethylene oxide to hydrophobic alcohol are reportedly 5, 7, 9, 12 and 15, respectively. While it is not intended that the invention be limited by any theories, it is noted that the most preferred surface active materials of this class are compounds in which the hydrophobic constituent is bonded at a secondary carbon, possibly providing a desirable degree of wettability in addition to outstanding emulsification characteristics.
An example of a preferred emulsifier in the ethoxylated aliphatic alcohol class which is derived from a primary liner C1245 aliphatic alcohol having an ethoxy/hydrophobe molar ratio of 12:1 is NEODOL 25-12 (T.M.). An example of an emulsifier derived from lauryl alcohol and having an ethyleneoxy/alcohol ratio of 12:1 is LIPAL 12 LA (T.M.). An example of an emulsifier derived from lauryl alcohol and having an ethoxy/hydrophobe molar ratio of 8:1 is known as TRYCOL LAL-8 (T.M.). Although alkyl polyethoxyethanols produced from linear primary hydrophobic alcohols, particularly those having 12 to 15 carbons, are also contempated for use in accordance with this invention, the secondary alcohol-derived compounds are preferred.
The emulsifier additive of this invention is added in an amount from 0.1% to 5.0% by weight based on the weight of the colored stock used.
It has been observed that the use of several of the most preferred commercially available emulsifiers, referred to above, tends to be accompanied by substantial foaming. It has been found that conventional defoamers can be used to control whatever may be considered an undesirable amount of foaming without adversely affecting the performance of the method of this invention with respect to the manufacture of high quality coated paper products from printed and coated paper furnish.
A number of TERGITOL l5-S-N commercially available emulsifiers are recited hereinbefore in which N is a number in the range 5-15. With the use of those commercially available materials identified by such names in which the N is the number 7, and greater numbers, the co-joint use of a defoamer is preferred.
It has also been found that ethoxylated alkyl phenols, such as IGEPAL CO 430, TRITON X-102," TRITON X-l 14, can be used in conjunction with the ethoxylated aliphatic alcohol type emulsifiers of this invention. These surface active materials have an effect on the extent of foaming and also have a highly beneficial effect on the dispersing of ink particles which are visible under 30 power magnification to such an extent that they are no longer visible under 30 power magnification. Preferred supplemental materials are ethoxylated alkyl phenols in which the alkyl substituent is octyl and nonyl. Alkyl phenoxy polethoxyethanols of this type are widely available surface active materials. The most preferred compounds of this class are those in which the alkyl substituent of the phenol group is tertiary octyl and in which the ratio of moles of ethylene oxide per mole of hydrophobe is in the range 78. Such most preferred materials are commercially available under the name TRITON X-l02 and TRITON X- 114. However, compounds of the ethoxylated alkyl phenol class having linear alkyl groups, such as octyl and nonyl, or in which the phenol is dialkyl substituted, are also contemplated for use as a supplemental emulsifier in accordance with this invention. A nonyl phenol with a 10.511 ethyle neoxy/alkyl phenol ratio is 1GB- PAL CO-710" (T.M.). A nbnylphenol having a 20:1 ratio of ethyleneoxy/alkyl phenol is SURPHONlC N-200 (T.M.). An octyl phenol-derived compound of this class having an ethyleneoxy/octyl phenol ratio of 15:1 is TRITON X- (T.M.).
The modifier additives which are used in accordance with this invention include the sodium and potassium salts of phosphoric and silicic acid although sodium salts are preferred because of cost considerations. Thus, any of the fully or partially neutralized sodium and potassium salts of orthophosphoric acid are preferred metal salts for use as modifier additive, in accordance with the method of this invention. Aqueous solutions of alkali metal silicate salts such as sodium silicate solutions are preferred forms of the modifier additives for use in accordance with this invention.
In accordance with an important aspect of the present invention, a formulation is provided for practicing the above described method. This formulation comprises an emulsifier additive of the type generally described above, a modifier additive of the type described above, or in lieu thereof, a material which by reaction in the slurry will provide the desired alkyl metal phosphate salts and/or alkyl metal silicate salts, and a suitable stabilizer which operates to prevent separation and/or freezing of the emulsifier and modifier additives during the handling, shipping and storage thereof.
A preferred formulation for use in the practice of the present invention which is especially suitable for use at high pH ranges (8-10) is comprised of the following:
Component Per Cent (by weight) Orthophosphoric acid 10-50 lsopropyl alcohol 5-20 In using the above formulation, a suitable base such as sodium hydroxide is added with the formulation to the pulper to produce the modifier additive (e.g. phosphate salt) in situ by reaction of such base with the phosphoric acid component.
The isopropyl alcohol component in the above formulation is used primarily to raise the cloud point to prevent separation in hot weather and to lower the freezing point in cold weather. Other suitable substitutes for this component will, accordingly, be apparent to those skilled in this art and would include, by way of example, only, ethyl alcohol, methyl alcohol and butyl alcohol.
A particularly preferred embodiment of the above described formulation is composed of 60% by weight of a suitable ethoxylated aliphatic alcohol such as TER- GlTOL 15-8-5," 30% by weight of orthophosphoric acid, and by weight of isopropyl alcohol.
Since certain of the water-soluble emulsifiers used in the present invention may produce foaming, it may be necessary to either incorporate a conventional antifoamer or defoamer constituent in the above formulations or, alternatively, separately add such defoamer to the pulper along with the formulation. Suitable antifoaming or defoamer materials will be apparent to those skilled in this art and, accordingly, a specific and detailed description thereof is not deemed necessary. Typically, however, these suitable anti-foaming or defoamer constituents would include those compositions which are currently commercially available under the trademark IGEPAL CO-430 and NETRONYX 622. These materials are used in amounts which are sufficient to control to the desired extent, or eliminate, foaming in the paper making system.
If desired, the alkali metal phosphates can be eliminated entirely and may be highly desirable in certain installations wherein it is considered beneficial to public waterway ecology to avoid phosphates. In such instances, alkali metal silicate, or mixtures of sodium silicate and sodium hydroxide (e.g. 50:50 mixtures) can be used with the emulsifier additive of this invention. The amount of modifier additive which is used is preferably the minimum amount which will provide a pH in the range 8-10, more preferably in the range 9-10.
In the following examples, and throughout the specification and claims, all amounts are expressed in parts by weight, all temperatures are expressed in degrees Fahrenheit, and all percents are expressed in percent by weight based on the weight of the material referred to, unless otherwise indicated.
EXAMPLE 1 Scrap colored paper from products made from chemical pulp, and comprising dixie cups, milk cartons, National Geographic magazines, and the like, was charged to a 2,000 lb. pulper and an emulsifier additive TER- GITOL -8-5, which was described hereinbefore, was added thereto at the rate of 30 lbs. of emulsifier per ton of scrap paper charged. Sufficient water is charged to provide a consistency of about 5%. An aqueous solution of sodium orthophosphate (10%) is added in an amount sufficient to adjust the pH of the aqueous system to 10.0. The resulting admixture was heated to a temperature of 180 F. The contents of the pulper are thoroughly beaten and agitated during the heating cycle. The scrap paper is gradually defibered and the ink is released in the aqueous phase. The. resulting fiber slurry-ink mixture is used in a cylinder machine process. It is noted that the slurry is not substantially diluted or cooled prior to its use in the cylinder machine. The resulting sheet is subsequently processed in a conventional coating method using a starch-clay coating, and the final product of the method of this invention is a white top liner of excellent quality free of waxy spots and visible ink specks.
EXAMPLE 2 The procedure of Example 1 is repeated, except that the emulsifier is added in the form of a prepared solution comprising TERGITOL l5-S-5, phosphoric acid (75%) and isopropyl alcohol in the weight ratio 60:30:10. Also, in the present example, sodium hydroxide is added instead of sodium phosphate to bring the pH to 10.0. Otherwise the conditions set forth in Example 1 are utilized and the product produced in accordance with the present example is substantially identi- 5 cal to the product produced in accordance with Example 1. It is noted that sodium phosphate is formed in situ during the pH adjustment step.
EXAMPLE 3 The procedure of Example 1 is repeated except that the emulsifier used in Example 1 is replaced by TER- GITOL 15-8-7 which was described hereinbefore, and furthermore, an effective amount of a defoamer mixture comprising IGEPAL CO-430 and NE- TRONYX 622 is used in conjunction therewith.
EXAMPLE 4 The procedure of Example 1 is repeated, except that instead of the sodium phosphate salts a 50:50 mixture of sodium hydroxide and sodium silicate is added to the aqueous system in an amount sufficient to raise the pH to 10.0. Thus, in the present example, no phosphates whatsoever are utilized. The results of the present example are substantially identical to the results achieved in the method of Example 1.
EXAMPLE 5 As the term is used herein, the so-called coating method is any well-known conventional coating method for example, roll, air knife, spray coating and tub sizing. Tub sizing is carried out on relatively dry paper, or on surfaces which may or may not have been previously or partly sized in the beating operation. The material used for this treatment must have adhesive properties. The principal substances used for adhesive properties in tub sizing methods include animal glue, modified starches and wash sizes. The operation of tub sizing is carried out either on the papermaking machine itself, or in a separate sizing press employing air drying. The paper contacts size material, then runs through rolls that remove the excess material and finally runs over drying rolls. This type of sizing operation is used further to enhance the water resistance of the paper, and especially to make it take ink evenly without blurring, even after erasures.
1n the method of this invention, the formed sheet, prior to coating, is in some instances lightly colored. However, any coloring remaining on the paper is so disposed that, after the coating step, the coloring is no longer visible and the product is uniformly white. Moreover, even though some of the paper used in the furnish, in all of the examples, included some waxed materials, the product of the process of this invention is free of wax specks or spots and is readily printable.
In the foregoing specification, a detailed description has been provided with respect to certain preferred embodiments of the present invention. It will be appreciated, however, that modifications and variations therefrom may be made by those skilled in the art without departing from the spirit and scope of this invention. Accordingly, the present invention is to be limited only by the scope of the appended claims.
We claim:
1. A method for manufacturing top liner and the like from printed and coated stock derived from chemical pulp, comprising the steps: agitating said stock together with an emulsifier and an additive in water to release the fibers and disperse the printing and coating constituent of said stock in said water, wherein the emulsifier is an ethoxylated aliphatic alcohol, and wherein said additive is selected from the group consisting of alkali metal phosphate salts, alkali metal silicate salts and mixtures thereof, said emulsifier being present in an effective amount in the range 0.1% to based on the weight of said stock, said additive being present in an amount from 0.0125% to 6.25% based on the weight of said stock, and said dispersing of said stock being conducted at an alkaline pH, said dispersing step resulting in the formation of a slurry wherein said stock as well as the printing and coating constituents thereof are dispersed; charging said slurry to a sheet forming machine and forming a paper sheet from the resulting released fibers; coating the resulting sheet with an opaque coatmg.
2. The method of claim 1 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 1 115 carbons, and wherein the average molar ratio of etylene oxide to hydrophobic alcohol is in the range 5:1 to :1.
3. The method of claim 1 wherein the ethoxylated aliphatic alcohol is one in which the hydrophobic portion is a mixture of straight chain aliphatic alcohols and the average mole ratio of the combined ethylene oxide to hydrophobic portion is in the range 1-50.
4. The method of claim 1 in which the emulsifier is an alkyl polyethyleneoxy ethanol in which the alkyl portion is derived from a secondary alcohol having 1 1-15 carbons and wherein the average molar ratio of combined ethylene oxide and secondary alcohol is in the range 5:1 to 9:1.
5. The method of claim 1 in which the emulsifier is derived from a water-insoluble secondary alcohol having a number of carbons in the range 11-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1, and in which an anti-foaming agent is also present during the agitation.
6. A composition for use in the manufacture of top liner and the like from printed and coated stock derived from chemical pulp, said composition consisting essentially of from 40% to 80% by weight of an ethoxylated aliphatic alcohol, from 10% to 50% by weight of a modifier additive selected from the class consisting of alkali metal phosphate salts, alkali metal silicate salts and mixtures thereof, and from 5% to by weight of a stabilizer which prevents separation of said ethoxylated aliphatic alcohol and said modifier additive during the shipping and handling of said composition.
7. The composition of claim 6 wherein said stabilizer is an alkyl alcohol having from 1 to 4 carbon atoms.
8. The composition of claim 6 wherein said modifier additive is orthophosphoric acid.
9. The composition of claim 6 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 1 1-15 carbons, and wherein the average molar ratio of ethylene oxide to hydrophobic alcohol is in the range 5:1 to 15:1.
10. The composition of claim 6 wherein the ethoxylated aliphatic alcohol is one in which the hydrophobic portion is a mixture of straight chain aliphatic alcohols and the average mole ratio of the combined ethylene oxide to hydrophobic portion is in the range 1-50.
11. The composition of claim 6 in which said ethoxylated aliphatic alcohol is an alkyl polyethyleneoxy ethanol in which the alkyl portion is derived from a secondary alcohol having 1 l-15 carbons and wherein the average molar ratio of combined ethylene oxide and secondary alcohol is in the range 5:1 to 9:1.
12. The composition of claim 6 in which said ethoxylated aliphatic alcohol is derived from a water-insoluble secondary alcohol having a number of carbons in the range 11-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1 and in which an anti-foaming agent is also present.
13. A composition for use in the manufacture of top liner and the like from printed and coated stock derived from chemical pulp, the active components in said composition consisting essentially of from 40% to by weight of an ethoxylated aliphatic alcohol and from 10% to 50% by weight of a modifier additive selected from the class consisting of alkali metal phosphate salts, alkali metal silicate salts and mixtures thereof.
14. The composition of claim 13 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 1 1-15 carbons, and wherein the average molar ratio of ethylene oxide to hydrophobic alcohol is in the range 5:1 to 15:1.
15. The composition of claim 13 wherein the ethoxylated aliphatic alcohol is one in which the hydrophobic portion is a mixture of straight chain aliphatic alcohols and the average mole ratio of the combined ethylene oxide to hydrophobic portion is in the range l50.
16. The composition of claim 13 in which said ethoxylated aliphatic alcohol is an alkyl polyethyleneoxy ethanol in which the alkyl portion is derived from a secondary alcohol having 1 l-l 5 carbons and wherein the average molar ratio of combined ethylene oxide and secondary alcohol is in the range 5:1 to 9:1.
17. The composition of claim 13 in which said ethoxylated aliphatic alcohol is derived from a waterinsoluble secondary alcohol having a number of carbons in the range ll-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1 and in which an anti-foaming agent is also present.
18. A composition for use in the manufacture of top liner and the like from printed and coated stock derived from chemical pulp, the active components in said composition consisting essentially of from 40% to 80% by weight of an ethoxylated aliphatic alcohol and from 10% to 50% by weight of phosphoric acid.
19. The composition of claim 18 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 11-15 carbons, and wherein the average molar ratio of ethylene oxide to hydrophobic alcohol is in the range 5:1 to 15:1.
ondary alcohol is in the range 5:1 to 9:1. 1
22. The composition of claim 18 in which said ethoxylated aliphatic alcohol is derived from a waterinsoluble secondary alcohol having a number of carbons in the range 11-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1 and in which an anti-foaming agent is also present.
Claims (21)
- 2. The method of claim 1 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 11-15 carbons, and wherein the average molar ratio of etylene oxide to hydrophobic alcohol is in the range 5:1 to 15:1.
- 3. The method of claim 1 wherein the ethoxylated aliphatiC alcohol is one in which the hydrophobic portion is a mixture of straight chain aliphatic alcohols and the average mole ratio of the combined ethylene oxide to hydrophobic portion is in the range 1-50.
- 4. The method of claim 1 in which the emulsifier is an alkyl polyethyleneoxy ethanol in which the alkyl portion is derived from a secondary alcohol having 11-15 carbons and wherein the average molar ratio of combined ethylene oxide and secondary alcohol is in the range 5:1 to 9:1.
- 5. The method of claim 1 in which the emulsifier is derived from a water-insoluble secondary alcohol having a number of carbons in the range 11-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1, and in which an anti-foaming agent is also present during the agitation.
- 6. A composition for use in the manufacture of top liner and the like from printed and coated stock derived from chemical pulp, said composition consisting essentially of from 40% to 80% by weight of an ethoxylated aliphatic alcohol, from 10% to 50% by weight of a modifier additive selected from the class consisting of alkali metal phosphate salts, alkali metal silicate salts and mixtures thereof, and from 5% to 20% by weight of a stabilizer which prevents separation of said ethoxylated aliphatic alcohol and said modifier additive during the shipping and handling of said composition.
- 7. The composition of claim 6 wherein said stabilizer is an alkyl alcohol having from 1 to 4 carbon atoms.
- 8. The composition of claim 6 wherein said modifier additive is orthophosphoric acid.
- 9. The composition of claim 6 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 11-15 carbons, and wherein the average molar ratio of ethylene oxide to hydrophobic alcohol is in the range 5:1 to 15:1.
- 10. The composition of claim 6 wherein the ethoxylated aliphatic alcohol is one in which the hydrophobic portion is a mixture of straight chain aliphatic alcohols and the average mole ratio of the combined ethylene oxide to hydrophobic portion is in the range 1-50.
- 11. The composition of claim 6 in which said ethoxylated aliphatic alcohol is an alkyl polyethyleneoxy ethanol in which the alkyl portion is derived from a secondary alcohol having 11-15 carbons and wherein the average molar ratio of combined ethylene oxide and secondary alcohol is in the range 5:1 to 9:1.
- 12. The composition of claim 6 in which said ethoxylated aliphatic alcohol is derived from a water-insoluble secondary alcohol having a number of carbons in the range 11-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1 and in which an anti-foaming agent is also present.
- 13. A composition for use in the manufacture of top liner and the like from printed and coated stock derived from chemical pulp, the active components in said composition consisting essentially of from 40% to 80% by weight of an ethoxylated aliphatic alcohol and from 10% to 50% by weight of a modifier additive selected from the class consisting of alkali metal phosphate salts, alkali metal silicate salts and mixtures thereof.
- 14. The composition of claim 13 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 11-15 carbons, and wherein the average molar ratio of ethylene oxide to hydrophobic alcohol is in the range 5:1 to 15:1.
- 15. The composition of claim 13 wherein the ethoxylated aliphatic alcohol is one in which the hydrophobic portion is a mixture of straight chain aliphatic alcohols and the average mole ratio of the combined ethylene oxide to hydrophobic portion is in the range 1-50.
- 16. The composition of claim 13 in which said ethoxylateD aliphatic alcohol is an alkyl polyethyleneoxy ethanol in which the alkyl portion is derived from a secondary alcohol having 11-15 carbons and wherein the average molar ratio of combined ethylene oxide and secondary alcohol is in the range 5:1 to 9:1.
- 17. The composition of claim 13 in which said ethoxylated aliphatic alcohol is derived from a water-insoluble secondary alcohol having a number of carbons in the range 11-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1 and in which an anti-foaming agent is also present.
- 18. A composition for use in the manufacture of top liner and the like from printed and coated stock derived from chemical pulp, the active components in said composition consisting essentially of from 40% to 80% by weight of an ethoxylated aliphatic alcohol and from 10% to 50% by weight of phosphoric acid.
- 19. The composition of claim 18 wherein the ethoxylated aliphatic alcohol is a hydrophobic secondary alcohol having from 11-15 carbons, and wherein the average molar ratio of ethylene oxide to hydrophobic alcohol is in the range 5:1 to 15:1.
- 20. The composition of claim 18 wherein the ethoxylated aliphatic alcohol is one in which the hydrophobic portion is a mixture of straight chain aliphatic alcohols and the average mole ratio of the combined ethylene oxide to hydrophobic portion is in the range 1-50.
- 21. The composition of claim 18 in which said ethoxylated aliphatic alcohol is an alkyl polyethyleneoxy ethanol in which the alkyl portion is derived from a secondary alcohol having 11-15 carbons and wherein the average molar ratio of combined ethylene oxide and secondary alcohol is in the range 5:1 to 9:1.
- 22. The composition of claim 18 in which said ethoxylated aliphatic alcohol is derived from a water-insoluble secondary alcohol having a number of carbons in the range 11-15, and in which the emulsifier has an average molar ratio of combined ethylene oxide to said secondary alcohol in the range 7:1 to 15:1 and in which an anti-foaming agent is also present.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17240671 US3808089A (en) | 1971-08-17 | 1971-08-17 | Process and composition for manufacturing top liner and the like from printed and coated stock |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17240671 US3808089A (en) | 1971-08-17 | 1971-08-17 | Process and composition for manufacturing top liner and the like from printed and coated stock |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3808089A true US3808089A (en) | 1974-04-30 |
Family
ID=22627583
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US17240671 Expired - Lifetime US3808089A (en) | 1971-08-17 | 1971-08-17 | Process and composition for manufacturing top liner and the like from printed and coated stock |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3808089A (en) |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3932206A (en) * | 1972-04-26 | 1976-01-13 | Garden State Paper Co., Inc. | Process for de-inking printed waste cellulosic fibrous material |
| US4162186A (en) * | 1976-12-15 | 1979-07-24 | Desoto, Inc. | Alkaline surfactant system for de-inking printed fibrous material |
| DE2833452A1 (en) * | 1978-07-29 | 1980-02-07 | Friedrich J Dipl Ing Zucker | PAPER FOR PACKAGING PURPOSES AND METHOD FOR THE PRODUCTION THEREOF |
| US4518459A (en) * | 1979-11-13 | 1985-05-21 | Economics Laboratory, Inc. | Methods of deinking secondary fibers |
| US4666558A (en) * | 1985-12-11 | 1987-05-19 | Shell Oil Company | Process for newspaper deinking using low-foaming surfactant deinking agent |
| US4935096A (en) * | 1988-12-06 | 1990-06-19 | Garden State Paper Company, Inc. | Process for the deinking of cellulosic materials |
| US4997523A (en) * | 1990-06-20 | 1991-03-05 | Betz Panerchem, Inc. | Method for effectively breaking up latex-coated paper during pulping to decrease the potential for white pitch deposition |
| US5314580A (en) * | 1992-07-08 | 1994-05-24 | Mauvin Material & Chemical Processing Limited | Process for the removal of ink, resin, and adhesive residues from paper, textile fabrics and solid surfaces |
| US5412090A (en) * | 1994-02-02 | 1995-05-02 | Bendiner; Bernard | Hydrous cellulose pulp for non paper products |
| US5840249A (en) * | 1997-02-28 | 1998-11-24 | Bendiner; Bernard | Preservative for organic materials |
| US5876559A (en) * | 1991-06-25 | 1999-03-02 | International Paper Company | Deinking of impact and non-impact printed paper by an agglomeration process |
| US6103294A (en) * | 1997-02-28 | 2000-08-15 | Preservation Products, Inc. | Preservative for digestible food and beverage products |
| US6171550B1 (en) | 1997-02-28 | 2001-01-09 | Preservation Products, Llc | Non-toxic base ingredient for consumer products |
| US20040065419A1 (en) * | 2002-10-04 | 2004-04-08 | Vicente Lasmarias | Removal of contaminants from recycled paper fibers |
| US6784146B1 (en) | 2000-10-27 | 2004-08-31 | Kemira Chemicals, Inc. | Deinking method and composition for wastepaper |
| US20050031838A1 (en) * | 2003-08-06 | 2005-02-10 | Spectra Systems Corporation | Taggant security system for paper products as a deterrent to counterfeiting |
| US20050142319A1 (en) * | 2003-12-23 | 2005-06-30 | Kari Virtanen | Thin polyethylene pressure sensitive labels |
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|---|---|---|---|---|
| US2753309A (en) * | 1951-10-27 | 1956-07-03 | Pioneer Chemical Works Inc | Defoaming agents |
| US3056713A (en) * | 1952-02-09 | 1962-10-02 | Fmc Corp | Process for the regeneration of waste paper |
| US3069308A (en) * | 1960-04-20 | 1962-12-18 | Petrolite Corp | Oxyalkylated alcohol process |
| US3158531A (en) * | 1961-08-18 | 1964-11-24 | Rohrer Ernst | Process for the production of waterproof materials from waste paper containing bitumen and/or wax |
| US3630929A (en) * | 1969-01-17 | 1971-12-28 | Lever Brothers Ltd | Fast dissolving nonaqueous built liquid detergent compositions |
-
1971
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US2753309A (en) * | 1951-10-27 | 1956-07-03 | Pioneer Chemical Works Inc | Defoaming agents |
| US3056713A (en) * | 1952-02-09 | 1962-10-02 | Fmc Corp | Process for the regeneration of waste paper |
| US3069308A (en) * | 1960-04-20 | 1962-12-18 | Petrolite Corp | Oxyalkylated alcohol process |
| US3158531A (en) * | 1961-08-18 | 1964-11-24 | Rohrer Ernst | Process for the production of waterproof materials from waste paper containing bitumen and/or wax |
| US3630929A (en) * | 1969-01-17 | 1971-12-28 | Lever Brothers Ltd | Fast dissolving nonaqueous built liquid detergent compositions |
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| Title |
|---|
| Stephenson, J. Newell; Pulp and Paper Manufacture; Vol. 2 and 3, McGraw Hill Book Co., N.Y., N.Y., 1951, Vol. 2 page 148, Vol 3, 758 759. * |
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3932206A (en) * | 1972-04-26 | 1976-01-13 | Garden State Paper Co., Inc. | Process for de-inking printed waste cellulosic fibrous material |
| US4162186A (en) * | 1976-12-15 | 1979-07-24 | Desoto, Inc. | Alkaline surfactant system for de-inking printed fibrous material |
| DE2833452A1 (en) * | 1978-07-29 | 1980-02-07 | Friedrich J Dipl Ing Zucker | PAPER FOR PACKAGING PURPOSES AND METHOD FOR THE PRODUCTION THEREOF |
| US4518459A (en) * | 1979-11-13 | 1985-05-21 | Economics Laboratory, Inc. | Methods of deinking secondary fibers |
| US4666558A (en) * | 1985-12-11 | 1987-05-19 | Shell Oil Company | Process for newspaper deinking using low-foaming surfactant deinking agent |
| US4935096A (en) * | 1988-12-06 | 1990-06-19 | Garden State Paper Company, Inc. | Process for the deinking of cellulosic materials |
| US4997523A (en) * | 1990-06-20 | 1991-03-05 | Betz Panerchem, Inc. | Method for effectively breaking up latex-coated paper during pulping to decrease the potential for white pitch deposition |
| US5876559A (en) * | 1991-06-25 | 1999-03-02 | International Paper Company | Deinking of impact and non-impact printed paper by an agglomeration process |
| US5314580A (en) * | 1992-07-08 | 1994-05-24 | Mauvin Material & Chemical Processing Limited | Process for the removal of ink, resin, and adhesive residues from paper, textile fabrics and solid surfaces |
| US5412090A (en) * | 1994-02-02 | 1995-05-02 | Bendiner; Bernard | Hydrous cellulose pulp for non paper products |
| WO1995020940A1 (en) * | 1994-02-02 | 1995-08-10 | Natural Fibers, Ltd. | Hydrous cellulose pulp for non paper products |
| US5840249A (en) * | 1997-02-28 | 1998-11-24 | Bendiner; Bernard | Preservative for organic materials |
| US6103294A (en) * | 1997-02-28 | 2000-08-15 | Preservation Products, Inc. | Preservative for digestible food and beverage products |
| US6171550B1 (en) | 1997-02-28 | 2001-01-09 | Preservation Products, Llc | Non-toxic base ingredient for consumer products |
| US6784146B1 (en) | 2000-10-27 | 2004-08-31 | Kemira Chemicals, Inc. | Deinking method and composition for wastepaper |
| US20040065419A1 (en) * | 2002-10-04 | 2004-04-08 | Vicente Lasmarias | Removal of contaminants from recycled paper fibers |
| US20050031838A1 (en) * | 2003-08-06 | 2005-02-10 | Spectra Systems Corporation | Taggant security system for paper products as a deterrent to counterfeiting |
| US20050142319A1 (en) * | 2003-12-23 | 2005-06-30 | Kari Virtanen | Thin polyethylene pressure sensitive labels |
| US7399509B2 (en) * | 2003-12-23 | 2008-07-15 | Kari Virtanen | Thin polyethylene pressure sensitive labels |
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