US3096231A - Method of manufacturing paper from partially esterified cellulose fibers - Google Patents
Method of manufacturing paper from partially esterified cellulose fibers Download PDFInfo
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- US3096231A US3096231A US22711A US2271160A US3096231A US 3096231 A US3096231 A US 3096231A US 22711 A US22711 A US 22711A US 2271160 A US2271160 A US 2271160A US 3096231 A US3096231 A US 3096231A
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- United States
- Prior art keywords
- paper
- resin
- cellulose fibers
- acid
- polyamide
- 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
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- 229920003043 Cellulose fiber Polymers 0.000 title description 10
- 238000004519 manufacturing process Methods 0.000 title description 4
- 239000000835 fiber Substances 0.000 claims description 33
- 239000011347 resin Substances 0.000 claims description 30
- 229920005989 resin Polymers 0.000 claims description 30
- 239000004952 Polyamide Substances 0.000 claims description 17
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 17
- 239000000194 fatty acid Substances 0.000 claims description 17
- 229930195729 fatty acid Natural products 0.000 claims description 17
- 150000004665 fatty acids Chemical group 0.000 claims description 17
- 229920002647 polyamide Polymers 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 229920002678 cellulose Polymers 0.000 claims description 16
- 239000001913 cellulose Substances 0.000 claims description 16
- 229920001187 thermosetting polymer Polymers 0.000 claims description 15
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 9
- 239000000725 suspension Substances 0.000 claims description 8
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 229920001281 polyalkylene Polymers 0.000 claims description 6
- 229920000768 polyamine Polymers 0.000 claims description 6
- 239000007900 aqueous suspension Substances 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
- 239000011707 mineral Substances 0.000 claims description 3
- 150000001412 amines Chemical group 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 150000003335 secondary amines Chemical group 0.000 claims 1
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 14
- 125000002091 cationic group Chemical group 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 10
- 239000002002 slurry Substances 0.000 description 10
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 8
- 239000002585 base Substances 0.000 description 7
- 238000009740 moulding (composite fabrication) Methods 0.000 description 7
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 108010010803 Gelatin Proteins 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 125000005313 fatty acid group Chemical group 0.000 description 5
- 229920000159 gelatin Polymers 0.000 description 5
- 239000008273 gelatin Substances 0.000 description 5
- 235000019322 gelatine Nutrition 0.000 description 5
- 235000011852 gelatine desserts Nutrition 0.000 description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
- 229920001131 Pulp (paper) Polymers 0.000 description 4
- -1 SILVER HALIDE Chemical class 0.000 description 4
- 235000021355 Stearic acid Nutrition 0.000 description 4
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 4
- 229940063655 aluminum stearate Drugs 0.000 description 4
- 239000000908 ammonium hydroxide Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- 239000008117 stearic acid Substances 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 3
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical group [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 3
- 229910001864 baryta Inorganic materials 0.000 description 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 3
- 239000013055 pulp slurry Substances 0.000 description 3
- 238000004513 sizing Methods 0.000 description 3
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- DTCCVIYSGXONHU-CJHDCQNGSA-N (z)-2-(2-phenylethenyl)but-2-enedioic acid Chemical compound OC(=O)\C=C(C(O)=O)\C=CC1=CC=CC=C1 DTCCVIYSGXONHU-CJHDCQNGSA-N 0.000 description 1
- OILSMOCIMSQVCU-UHFFFAOYSA-N 2-hexadecylicos-1-ene-1,3-dione Chemical compound CCCCCCCCCCCCCCCCCC(=O)C(=C=O)CCCCCCCCCCCCCCCC OILSMOCIMSQVCU-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical group NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 238000005213 imbibition Methods 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H5/00—Special paper or cardboard not otherwise provided for
- D21H5/12—Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials
- D21H5/14—Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials of cellulose fibres only
- D21H5/141—Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials of cellulose fibres only of fibrous cellulose derivatives
- D21H5/145—Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials of cellulose fibres only of fibrous cellulose derivatives cellulose esters
- D21H5/146—Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials of cellulose fibres only of fibrous cellulose derivatives cellulose esters cellulose acetate
-
- 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
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
- D21H23/76—Processes or apparatus for adding material to the pulp or to the paper characterised by choice of auxiliary compounds which are added separately from at least one other compound, e.g. to improve the incorporation of the latter or to obtain an enhanced combined effect
- D21H23/765—Addition of all compounds to the pulp
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/16—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
- D21H11/20—Chemically or biochemically modified fibres
-
- 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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
- D21H17/42—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups anionic
- D21H17/43—Carboxyl groups or 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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/54—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
- D21H17/55—Polyamides; Polyaminoamides; Polyester-amides
-
- 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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/63—Inorganic compounds
- D21H17/66—Salts, e.g. alums
Definitions
- This invention relates to improving the wet strength and alcohol tolerance of paper prepared from partially esterified cellulose fibers.
- One object of our invention is to increase the wet strength of partially esterified paper by means especially adapted for use in paper composed of partially esterified fibers. Another object of our invention is to provide a paper which not only is characterized by superior wet strength but also exhibits tolerance to coating compositions containing alcohol. A further object of our invention is to provide a means for increasing the wet strength of partially esteri-fied fiber pap-er which does not adversely affect other properties of the paper. A still further object of our invention is to provide a photographic paper base having highly desirable charcteristics. Other objects of our invention will appear herein.
- Paper in accordance with our invention, is conveniently prepared by first heating partially esterified wood pulp fiber such as one having an apparent acetyl content of to the desired slowness for papering-out use, thus forming a pulp slurry. To this slurry is first added an aqueous solution of sodium stearate.
- Efiicient sizing is obtained if this is added at the rate of OAS-4% fatty acid solids based on fiber Weight.
- some other fatty acid may be used such as palmitic acid.
- ammonium hydroxide might be employed rather than sodium hydroxide.
- the water employed in diluting the slurry such as white water
- has a certain degree of alkalinity such ice that the pH would be raised above 7.0
- thermosetting polyamide epichlorohydrin resin such as described in U.S. Patents No. 2,926,154 or 2,926,1 16 of Keim.
- This resin may be added to the slurry at any time prior to applying it to the wire of the paper machine prefer-ably just prior thereto.
- This resin may be employed in a percentage within the range of 0.1-5 and desirably (LS-3% based on the fiber, the range of 1-2% being optimum. It is desirable that the pH of the slurry be above 4.5 to obtain good curing of the thermosetting resin when in the paper.
- the slurry is applied to the wire of the paper machine in the convention manner and the paper formed is dried.
- the paper obtained be tub sized such as with a styrene-maleic acid or maleic anhydride type resin as described and claimed in application Serial No. 22,710 of our and Alan Gray, filed of even date.
- the paper thus sized may also be conveniently subjected to a tub sizing with a gelatin solution. It has been found advantageous to include in this gelatin solution aluminum chloride or aluminum sulfate, this further treatment still further improving the alcohol penetration resistance of the paper.
- a heat treatment such as by passing through an oven or by subjecting to infrared radiation as more fully described in application Serial No. 22,695 of us and Alan Gray of even date. It is desirable to calender the paper with hot rolls.
- the sodium stearate size which is used in preparing the paper in accordance with our invention is made up by mixing alkali and fatty acid together such as to form, for instance, the salt thereof usually sodium stearate.
- alkali and fatty acid such as to form, for instance, the salt thereof usually sodium stearate.
- 62 /2 pounds of NaOH is dissolved in 1,250 gallons of water at l90 F. and 200 pounds of commercial stearic acid (29% palmitic, 69% stearic, 2% other fatty acid) is added thereto.
- the final solution contains 1.9% of fatty acid solids or 2.5% total solids.
- the NaOH is present in 114% excess in this solution.
- the NaOH used in preparing this size may be employed in stoichiometric amount or it may be present in smaller or larger excess than specified.
- the amount of alkali used is preferably sufficient to form a solution of all of the fatty acid employed.
- Ammonium hydroxide may be used as the alkali material, in which case it is ordinarily desirable to employ an excess of base.
- stearic acid some other fatty acid such as lau-ric, myristic or the like may be employed.
- the paper in accordance with our invention is prepared from fibers which are predominantly partially acylated such as having an apparent acetyl content of 15-25%. These fibers may have been acylated or some other lower fatty acid radical may have been imparted either as a portion of the acyl or instead of the acetyl. For instance, the cellulose fibers may have propionyl or bu-tyryl groups chemically combined therewith providing the acyl content is Within the range of 15-25%.
- the fibers of the paper prepared in accordance with our invention may .be entirely partially esterified fibers or there may be some content of cellulose or other fibers therein. It is desirable, however, that the partially esterified fibers constitute 7 5l00% of the fiber content of the paper.
- the accompanying drawing illustrating photographic paper in accordance with our invention shows in section the arrangement of layers therein in which the paper base is internally sized with aluminum salt of a higher fatty acid and cationic thermoset polyamide-epichlorohydrin resin. Applied to one face of the paper is a baryta coating over which is applied a silver halide photographic emulsion.
- Example 1 One pound of wood pulp acetylated to an acetyl content of 20% was beaten in a Valley beater to a Williams slowness of 30 seconds. A sample of the pulp slurry thus obtained was mixed with /2 cc. per gm. of pulp of a solution of sodium stearate containing 1.9% fatty acid solids. Following this, a aqueous solution of aluminum chloride was added to bring the mass to a pH of 4.5. Ammonium hydroxide was then added to impart a pH of 8. This was followed by the addition of starch size and of a 2% solution of a cationic thermosetting polyamide-epichlorohydrin resin as described in Example 1 of Us. Patent No. 2,926,154, this resin being added in the amount of 2% based on the weight of the fiber used. The slurry was then applied to a paper making screen and paper was prepared therefrom in the conventional manner.
- Paper was prepared from this slurry in the conventional To 3,000 pounds of a slurry of wood pulp cellulose having an acetyl content of approximately 20% while in a chemical mixing chest was added 250 gallons of sodium stearate solution which had 1.33% fatty acid solids based upon fiber weight.
- Aluminum chloride was then added to the mass to reach a pH within the range of 6.0 to 6.5. To prevent the pH in the head box going above 7.0, aluminum chloride was added at that point in sulficient amount to maintain the pH adjustment following which there was added cationic thermosetting polyamideepichlorohydrin resin in the form of its aqueous solution to supply 2% of resin based on the weight of the partially acylated fiber.
- the fiber slurry was applied to the wire of a paper machine in the conventional manner for making paper and the paper sheet thus obtained was calendered on hot rolls.
- the sheet thus prepared was tub sized with an aqueous solution of styrene-maleic anhydride resin and Was then subjected to a temperature of 350 F. for 10 sec. to 2 minutes.
- a paper was obtained having good characteristics both as regards wet strength and resistance to any derogatory effect upon the application thereto of coatings containing butyl alcohol.
- Example 3 Papers were prepared from partially acetylated fibers (acetyl about 20%) internally sized with aluminum stearate, stearic acid and cationic thermosetting polyamide-epichlorohydrin resin as described herein and surface sized with styrene-maleic anhydride resin and gelatin.
- Samples of these papers were baryta coated with a composition of 9.6-14.4 parts B2180 and 1 part gelatin in 35-40% solids concentration in water-butyl alcohol (96:4). This coating may contain a gelatin hardener.
- the baryta coating was dried and super calendered. There was then applied thereover a gelatin-silver halide photographic emulsion layer.
- the emulsion employed may contain an alcohol therein without any adverse effect upon the paper base.
- the papers thus obtained had excellent dimensional stability, were free of curl and could be processed in photographic processing solutions and dried at high rates without embrittlcment or change in physical properties.
- a method of preparing paper which comprises forming an aqueous suspension of cellulose fibers the cellulose of which contains 15-25% of lower fatty acid groups chemically combined therewith adding to this suspension in that order a water soluble salt of a higher fatty acid, a water soluble aluminum salt of a strong mineral acid and a water soluble cationic thermosetting resin formed by reacting epichlorohydrin with a polyamide of C to C saturated aliphatic dibasic carboxylic acid and from about 0.8 to about 1.4 moles per mole of dibasic acid of a polyalkylene polyamine at a temperature from about 45 C.
- said polyamide containing secondary amine groups, the ratio of epichlorohydrin to secondary amine groups of said polyamide being from about 05-1 to about 1.8-1, adsorbing 0.1-5% approximately of said resin on said cellulose fibers, forming the cellulose fibers suspension into a sheet and heating the sheet to cure the resin to a water insoluble state.
- a method of preparing paper which comprises forming an aqueous suspension of cellulose fibers the cellulose of which contains 15-25% of lower fatty acid groups chemically combined therewith, adding to the suspension in that order a water soluble salt of a higher fatty acid having a carbon content of 12-20 carbon atoms, a Water soluble aluminum salt of a strong mineral acid and a water soluble cationic thermosetting resin formed by reacting epichlorohydrin with a polyamide of C to C saturated aliphatic dibasic carboxylic acid and from about 0.8 to about 1.4 moles per mole of dibasic acid of a polyalkylene polyamine at a temperature from about 45 C.
- said polyamide containing secondary amine groups, the ratio of epichlorohydrin to secondary amine groups of said polyamide being from about 0.5-1 to about 1.8-1, adsorbing 0.1-5 approximately of said resin on said cellulose fibers, forming the cellulose fibers suspension into a sheet and heating the sheet to cure the resin to a water insoluble state.
- a method of preparing paper which comprises form ing an aqueous suspension of cellulose fibers the cellulose of which contains 15-25% acetyl chemically combined therewith, adding to the suspension in that order, sodium stearate in aqueous solution, aluminum chloride in solution and a water soluble cationic thermosetting resin formed by reacting epichlorohydrin with a polyamide of a C to C saturated aliphatic dicarboxylic acid and from about 0.8 to about 1.4 moles per mole of dibasic acid of a polyalkylene polyamine at a temperature of from about 45 C.
- said polyamide containing secondary amine groups the ratio of epichlorohydrin to secondary amine being 0.5-1 to about 1.8-1, adsorbing about 0.1-5% approximately of said resin on said suspended pulp, forming the cellulose suspension into a sheet and heating the sheet to cure the resin to a water insoluble state.
- Paper comprising sheeted fibers of cellulose which cellulose contains 15-25% of fatty acid groups of 2-4 carbon atoms chemically combined therewith containing an aluminum salt of a higher fatty acid of 12-20 carbon atoms and about 0.1-5 based on the dry weight, of a cationic thermoset resin, said resin having been obtained by adding to said fibers of cellulose a water-soluble reaction product of epichlorohydrin, and a polyamide containing secondary amine groups, the ratio of epichlorohydrin to secondary amine groups of said polyamide being from about 0.5-1 to about 1.8-1, said polyamide being obtained by heating together at a temperature from about 110 C. to about 250 C.
- Paper comprising sheeted fibers of cellulose which cellulose contains 25% of fatty acid groups of 2-4 carbon atoms chemically combined therewith, containing an aluminum salt of a higher fatty acid of 12-20 carbon atoms and about 0.1-5% based on its dry weight of a cationic thermoset polyamide-epichlorohydrin resin obtained by (1) reacting a C to C saturated aliphatic dibasic dicarboxylic acid with from about 0.8 to about 1.4 moles per mole of dibasic acid of a polyalkylene polyamine at a temperature from about 110 C. to about 150 C. to form a polyarm'de containing secondary amine groups and (2) reacting the polyamide with epichlorohydrin at a temperature from about C. to about C.
Landscapes
- Paper (AREA)
Description
y 1963 H. GRIGGS ETAL 3,096,231
W. METHOD OF MANUFACTURING PAPER FROM PARTIALLY ESTERIFIED CELLULOSE FIBERS Filed April 18. 1960 SILVER HALIDE fiHOTOGRAPHIC EMULSlON LAYER ADHERENT fiARYTA COATING 7 PA PER BASE CONTAINING AL STEARATEand CATIONIC THERMOSET POLYAMIDE- EPICH LOR HYDRIN R E S I N Wi l liam H .Griggs Ray/1D. Za ffrann IN VEN TORS' 4b AIIOR m METHOD OF MANUFACTURING PAPER FROM PARTIALLY ESTEREFHED CELLULUSE FHEERS William H. Grlggs and Ralph D. Zaffrann, Rochester,
N.Y., assignors to Eastman Kodak Company, Rochester, N.Y., a corporation of New Jersey Filed Apr. 18, 193i Eer. No. 22,711 9 Claims. (Cl. 162-157) This invention relates to improving the wet strength and alcohol tolerance of paper prepared from partially esterified cellulose fibers.
Richter and Herdle application Serial No. 755,418, [filed August 18, 1958, describes paper useful for photographic purposes, the fibers of which have lower fatty acid groups chemically combined therewith. Paper, the fibers of which have been partially esterified, is characterized by good stability and resistance to imbibition of aqueous salt solutions. It is desirable, however, to improve the wet strength of paper of this type. Often, however, materials regarded as useful for imparting good wet strength to ordinary paper are not effective to the same degree when employed in paper of partially esterified fibers. It is desirable that paper prepared from partially esterified fibers particularly for photographic purposes exhibit tolerance to coating solutions containing alcohol. Many materials which have been suggested for paper sizing do not impart this characteristic to partially esterified paper. In many cases, wet strength improvers in paper have rendered that paper brittle or otherwise altered the properties thereof so that increase in wet strength has been accomplished by the sacrifice of some other desirable property.
One object of our invention is to increase the wet strength of partially esterified paper by means especially adapted for use in paper composed of partially esterified fibers. Another object of our invention is to provide a paper which not only is characterized by superior wet strength but also exhibits tolerance to coating compositions containing alcohol. A further object of our invention is to provide a means for increasing the wet strength of partially esteri-fied fiber pap-er which does not adversely affect other properties of the paper. A still further object of our invention is to provide a photographic paper base having highly desirable charcteristics. Other objects of our invention will appear herein.
We have found that paper composed of partially esterified fibers is greatly improved in characteristics such as to render that paper valuable as a photographic paper base if there has been incorporated in that paper in its manufacture aluminum stearate or palmitate and a cationic thermosetting polyamide-epichlorohydrin resin of the type described in U.S. Patent No. 2,926,154. Paper, in accordance with our invention, is conveniently prepared by first heating partially esterified wood pulp fiber such as one having an apparent acetyl content of to the desired slowness for papering-out use, thus forming a pulp slurry. To this slurry is first added an aqueous solution of sodium stearate. Efiicient sizing is obtained if this is added at the rate of OAS-4% fatty acid solids based on fiber Weight. Instead of steric acid, some other fatty acid may be used such as palmitic acid. In making up this size, ammonium hydroxide might be employed rather than sodium hydroxide. After the sodium stearate has been thoroughly incorporated in the slurried fiber, there is added aluminum chloride or aluminum sulfate to precipitate the stearate size onto the fiber in the form of aluminum stearate (and stearic acid) and to reduce the pH to below 7 such as 6.0-6.5. This is conveniently accomplished in the mixing chest of the paper apparatus. If the water employed in diluting the slurry, such as white water, has a certain degree of alkalinity such ice that the pH would be raised above 7.0, it is desirable to reduce the pH below that figure by adding aluminum chloride or aluminum sulfate thereto.
There is then added to the slurry a solution of a cationic thermosetting polyamide epichlorohydrin resin such as described in U.S. Patents No. 2,926,154 or 2,926,1 16 of Keim. This resin may be added to the slurry at any time prior to applying it to the wire of the paper machine prefer-ably just prior thereto. This resin may be employed in a percentage within the range of 0.1-5 and desirably (LS-3% based on the fiber, the range of 1-2% being optimum. It is desirable that the pH of the slurry be above 4.5 to obtain good curing of the thermosetting resin when in the paper. The slurry is applied to the wire of the paper machine in the convention manner and the paper formed is dried. It is desirable that the paper obtained be tub sized such as with a styrene-maleic acid or maleic anhydride type resin as described and claimed in application Serial No. 22,710 of ourselves and Alan Gray, filed of even date. The paper thus sized may also be conveniently subjected to a tub sizing with a gelatin solution. It has been found advantageous to include in this gelatin solution aluminum chloride or aluminum sulfate, this further treatment still further improving the alcohol penetration resistance of the paper. After the paper has been tub sized as desired, it is then subjected to a heat treatment such as by passing through an oven or by subjecting to infrared radiation as more fully described in application Serial No. 22,695 of ourselves and Alan Gray of even date. It is desirable to calender the paper with hot rolls.
The sodium stearate size which is used in preparing the paper in accordance with our invention is made up by mixing alkali and fatty acid together such as to form, for instance, the salt thereof usually sodium stearate. As an example, 62 /2 pounds of NaOH is dissolved in 1,250 gallons of water at l90 F. and 200 pounds of commercial stearic acid (29% palmitic, 69% stearic, 2% other fatty acid) is added thereto. The final solution contains 1.9% of fatty acid solids or 2.5% total solids. The NaOH is present in 114% excess in this solution. If desired, the NaOH used in preparing this size may be employed in stoichiometric amount or it may be present in smaller or larger excess than specified. The amount of alkali used is preferably sufficient to form a solution of all of the fatty acid employed. Ammonium hydroxide may be used as the alkali material, in which case it is ordinarily desirable to employ an excess of base. Instead of stearic acid, some other fatty acid such as lau-ric, myristic or the like may be employed.
The paper in accordance with our invention is prepared from fibers which are predominantly partially acylated such as having an apparent acetyl content of 15-25%. These fibers may have been acylated or some other lower fatty acid radical may have been imparted either as a portion of the acyl or instead of the acetyl. For instance, the cellulose fibers may have propionyl or bu-tyryl groups chemically combined therewith providing the acyl content is Within the range of 15-25%. The fibers of the paper prepared in accordance with our invention may .be entirely partially esterified fibers or there may be some content of cellulose or other fibers therein. It is desirable, however, that the partially esterified fibers constitute 7 5l00% of the fiber content of the paper.
The accompanying drawing illustrating photographic paper in accordance with our invention shows in section the arrangement of layers therein in which the paper base is internally sized with aluminum salt of a higher fatty acid and cationic thermoset polyamide-epichlorohydrin resin. Applied to one face of the paper is a baryta coating over which is applied a silver halide photographic emulsion.
The following examples illustrate our invention:
Example 1 One pound of wood pulp acetylated to an acetyl content of 20% was beaten in a Valley beater to a Williams slowness of 30 seconds. A sample of the pulp slurry thus obtained was mixed with /2 cc. per gm. of pulp of a solution of sodium stearate containing 1.9% fatty acid solids. Following this, a aqueous solution of aluminum chloride was added to bring the mass to a pH of 4.5. Ammonium hydroxide was then added to impart a pH of 8. This was followed by the addition of starch size and of a 2% solution of a cationic thermosetting polyamide-epichlorohydrin resin as described in Example 1 of Us. Patent No. 2,926,154, this resin being added in the amount of 2% based on the weight of the fiber used. The slurry was then applied to a paper making screen and paper was prepared therefrom in the conventional manner.
For a control, one pound of wood pulp acetylated to an acetyl content of was beaten in 21 Valley heater to a Williams slowness of 30 seconds and the following materials were added to a sample of the resulting pulp slurry with proper mixing between additions: 7% starch, ammonium hydroxide to a pH of 8.0, 2% of cationic thermosetting polyamide-epichlorohydrin resin and /s% of stearoyl hexadecylethenone (alkyl ketene dimer). Paper was prepared from this slurry in the conventional To 3,000 pounds of a slurry of wood pulp cellulose having an acetyl content of approximately 20% while in a chemical mixing chest was added 250 gallons of sodium stearate solution which had 1.33% fatty acid solids based upon fiber weight. Aluminum chloride was then added to the mass to reach a pH within the range of 6.0 to 6.5. To prevent the pH in the head box going above 7.0, aluminum chloride was added at that point in sulficient amount to maintain the pH adjustment following which there was added cationic thermosetting polyamideepichlorohydrin resin in the form of its aqueous solution to supply 2% of resin based on the weight of the partially acylated fiber. The fiber slurry was applied to the wire of a paper machine in the conventional manner for making paper and the paper sheet thus obtained was calendered on hot rolls. The sheet thus prepared was tub sized with an aqueous solution of styrene-maleic anhydride resin and Was then subjected to a temperature of 350 F. for 10 sec. to 2 minutes. A paper was obtained having good characteristics both as regards wet strength and resistance to any derogatory effect upon the application thereto of coatings containing butyl alcohol.
Example 3 Papers were prepared from partially acetylated fibers (acetyl about 20%) internally sized with aluminum stearate, stearic acid and cationic thermosetting polyamide-epichlorohydrin resin as described herein and surface sized with styrene-maleic anhydride resin and gelatin. Samples of these papers were baryta coated with a composition of 9.6-14.4 parts B2180 and 1 part gelatin in 35-40% solids concentration in water-butyl alcohol (96:4). This coating may contain a gelatin hardener. The baryta coating was dried and super calendered. There was then applied thereover a gelatin-silver halide photographic emulsion layer. The emulsion employed may contain an alcohol therein without any adverse effect upon the paper base.
ther samples of the papers prepared as described were coated directly with gelatin-silver halide photographic emulsion layers. Emulsion compositions containing alcohol were found to have no adverse effect upon the paper base.
The papers thus obtained had excellent dimensional stability, were free of curl and could be processed in photographic processing solutions and dried at high rates without embrittlcment or change in physical properties.
We claim:
1. A method of preparing paper which comprises forming an aqueous suspension of cellulose fibers the cellulose of which contains 15-25% of lower fatty acid groups chemically combined therewith adding to this suspension in that order a water soluble salt of a higher fatty acid, a water soluble aluminum salt of a strong mineral acid and a water soluble cationic thermosetting resin formed by reacting epichlorohydrin with a polyamide of C to C saturated aliphatic dibasic carboxylic acid and from about 0.8 to about 1.4 moles per mole of dibasic acid of a polyalkylene polyamine at a temperature from about 45 C. to about 100 C., said polyamide containing secondary amine groups, the ratio of epichlorohydrin to secondary amine groups of said polyamide being from about 05-1 to about 1.8-1, adsorbing 0.1-5% approximately of said resin on said cellulose fibers, forming the cellulose fibers suspension into a sheet and heating the sheet to cure the resin to a water insoluble state.
2. A method of preparing paper which comprises forming an aqueous suspension of cellulose fibers the cellulose of which contains 15-25% of lower fatty acid groups chemically combined therewith, adding to the suspension in that order a water soluble salt of a higher fatty acid having a carbon content of 12-20 carbon atoms, a Water soluble aluminum salt of a strong mineral acid and a water soluble cationic thermosetting resin formed by reacting epichlorohydrin with a polyamide of C to C saturated aliphatic dibasic carboxylic acid and from about 0.8 to about 1.4 moles per mole of dibasic acid of a polyalkylene polyamine at a temperature from about 45 C. to about C., said polyamide containing secondary amine groups, the ratio of epichlorohydrin to secondary amine groups of said polyamide being from about 0.5-1 to about 1.8-1, adsorbing 0.1-5 approximately of said resin on said cellulose fibers, forming the cellulose fibers suspension into a sheet and heating the sheet to cure the resin to a water insoluble state.
3. A method of preparing paper which comprises form ing an aqueous suspension of cellulose fibers the cellulose of which contains 15-25% acetyl chemically combined therewith, adding to the suspension in that order, sodium stearate in aqueous solution, aluminum chloride in solution and a water soluble cationic thermosetting resin formed by reacting epichlorohydrin with a polyamide of a C to C saturated aliphatic dicarboxylic acid and from about 0.8 to about 1.4 moles per mole of dibasic acid of a polyalkylene polyamine at a temperature of from about 45 C. to about 100 C., said polyamide containing secondary amine groups, the ratio of epichlorohydrin to secondary amine being 0.5-1 to about 1.8-1, adsorbing about 0.1-5% approximately of said resin on said suspended pulp, forming the cellulose suspension into a sheet and heating the sheet to cure the resin to a water insoluble state.
4. A process according to claim 3 in which the alkylene polyamine is diethylene triamine.
5. A process according to claim 4 in which the dicarboxylic acid is adipic acid.
6. Paper comprising sheeted fibers of cellulose which cellulose contains 15-25% of fatty acid groups of 2-4 carbon atoms chemically combined therewith containing an aluminum salt of a higher fatty acid of 12-20 carbon atoms and about 0.1-5 based on the dry weight, of a cationic thermoset resin, said resin having been obtained by adding to said fibers of cellulose a water-soluble reaction product of epichlorohydrin, and a polyamide containing secondary amine groups, the ratio of epichlorohydrin to secondary amine groups of said polyamide being from about 0.5-1 to about 1.8-1, said polyamide being obtained by heating together at a temperature from about 110 C. to about 250 C. a C to C saturated aliphatic dibasic carboxylic acid and from about 0.8 to about 1.4 moles per mole of dibasic acid of a polyalkylene polyamide, and curing said resin to a Waterinsoluble state by heating after said fibers have been formed into sheets.
7. Paper comprising sheeted fibers of cellulose which cellulose contains 25% of fatty acid groups of 2-4 carbon atoms chemically combined therewith, containing an aluminum salt of a higher fatty acid of 12-20 carbon atoms and about 0.1-5% based on its dry weight of a cationic thermoset polyamide-epichlorohydrin resin obtained by (1) reacting a C to C saturated aliphatic dibasic dicarboxylic acid with from about 0.8 to about 1.4 moles per mole of dibasic acid of a polyalkylene polyamine at a temperature from about 110 C. to about 150 C. to form a polyarm'de containing secondary amine groups and (2) reacting the polyamide with epichlorohydrin at a temperature from about C. to about C. and at a ratio of epichlorohydrin to secondary amine groups of the polyamide to from about 0.51 to 1.8-1 to form a water-soluble cationic thermosetting resin which resin has been cured to a water-insoluble state by heating the paper after said fibers have been formed into sheets.
8. A paper product in accordance with claim 7 in which the aluminum salt of a higher fatty acid is aluminum stearate.
9. A paper product in accordance with claim 8 in which the dibasic carboxylic acid is a C to C saturated aliphatic dibasic carboxylic acid.
References Cited in the file of this patent UNITED STATES PATENTS 1,840,399 Lane Jan. 12, 1932 2,366,723 Galley Jan. 9, 1945 2,394,289 Boughton Feb. 5, 1946 2,913,356 Schroeder Nov. 17, 1959 2,926,154 Keim Feb. 23, 1960 3,015,537 Gray Jan. 2, 1962 FOREIGN PATENTS 535,932 Great Britain Apr. 28, 1941
Claims (1)
1. A METHOD OF PREPARING PAPER WHICH COMPRISES FORMING AN AQUEOUS SUSPENSION OF CELLULOSE FIBERS THE CELLULOSE OF WHICH CONTAINS 15-25% OF LOWER FATTY ACID GROUPS CHEMICALLY COMBINED THEREWITH ADDING TO THIS SUSPENSION IN THAT ORDER A WATER SOLUBLE SALT OF A HIGHER FATTY ACID, A WATER SLUBLE ALUMINUM SALT OF A STRONG MINERAL ACID AND A WATER SOLUBLE CATIONIC THERMOSETTING RESIN FORMED BY REACTING EPICHLOROHYDRIN WITH A PLYAMIDE OF C3 TO C10 SATURATED ALIPHATIC DIBASIC CARBOXYLIC ACID AND FROM ABOUT 0.8 TO ABOUT 1.4 MOLES PER MOLE OF DIBASIC ACID OF A POLYALKYLENE POLYAMINE AT A TEMPERATURE FROM ABOUT 45*C. TO ABOUT 100*C., SAID POLYAMIDE CONTAINING SECONDARY AMINE GROUPS, THE RATIO OF EPICHLOROHYDRIN TO SECNDARY AMINE GROUPS OF SAID POLYAMIDE BEING FROM ABOUT 0.5-1 TO ABOUT 1.8-1, ADSORBING 0.1-5% APPROXIMATELY OF SAID RESIN ON SAID CELLULOSE FIBERS, FROMING THE CELLULOSE FIBERS SUSPENSION INTO A SHEET AND HEATING THE SHEET TO CURE THE RESIN TO A WATER INSOLUBLE STATE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22711A US3096231A (en) | 1960-04-18 | 1960-04-18 | Method of manufacturing paper from partially esterified cellulose fibers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22711A US3096231A (en) | 1960-04-18 | 1960-04-18 | Method of manufacturing paper from partially esterified cellulose fibers |
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|---|---|
| US3096231A true US3096231A (en) | 1963-07-02 |
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| US22711A Expired - Lifetime US3096231A (en) | 1960-04-18 | 1960-04-18 | Method of manufacturing paper from partially esterified cellulose fibers |
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| US (1) | US3096231A (en) |
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| US3186900A (en) * | 1962-07-13 | 1965-06-01 | Hercules Powder Co Ltd | Sizing paper under substantially neutral conditions with a preblend of rosin and cationic polyamide-epichlorohydrin resin |
| US3200033A (en) * | 1961-11-02 | 1965-08-10 | Battelle Institut E V | Method of making paper and non-woven fabric from synthetic fibers |
| US3250619A (en) * | 1962-06-25 | 1966-05-10 | Eastman Kodak Co | Stain-free paper |
| US3878038A (en) * | 1971-03-18 | 1975-04-15 | Feldmuehle Anlagen Prod | Stiff light-weight paper |
| FR2406232A1 (en) * | 1977-10-14 | 1979-05-11 | Eastman Kodak Co | METHOD OF MANUFACTURING A PHOTOGRAPHIC PRODUCT ON A PAPER SUPPORT |
| US4237206A (en) * | 1977-12-21 | 1980-12-02 | Fuji Photo Film Co., Ltd. | Photographic paper base with seperate reflective layer |
| US4288287A (en) * | 1979-01-16 | 1981-09-08 | Mitsubishi Paper Mills, Ltd. | Photographic support |
| US6361651B1 (en) | 1998-12-30 | 2002-03-26 | Kimberly-Clark Worldwide, Inc. | Chemically modified pulp fiber |
| US6743573B1 (en) * | 2003-02-03 | 2004-06-01 | Eastman Kodak Company | Black and white silver halide display elements having good light stability |
| US20150275438A1 (en) * | 2014-03-27 | 2015-10-01 | Georgia-Pacific Chemicals Llc | Wet strengthened fiber products, wet strengthening resins, and methods for making and using same |
| WO2016022879A1 (en) * | 2014-08-07 | 2016-02-11 | Georgia-Pacific Chemicals Llc | Strengthening resins for paper products |
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| US20150275438A1 (en) * | 2014-03-27 | 2015-10-01 | Georgia-Pacific Chemicals Llc | Wet strengthened fiber products, wet strengthening resins, and methods for making and using same |
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