US3015537A - Paper having improved characteristics and its preparation - Google Patents
Paper having improved characteristics and its preparation Download PDFInfo
- Publication number
- US3015537A US3015537A US580722A US58072256A US3015537A US 3015537 A US3015537 A US 3015537A US 580722 A US580722 A US 580722A US 58072256 A US58072256 A US 58072256A US 3015537 A US3015537 A US 3015537A
- Authority
- US
- United States
- Prior art keywords
- paper
- water
- dried
- content
- wet
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000002360 preparation method Methods 0.000 title description 5
- 239000007788 liquid Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 17
- 229910052751 metal Inorganic materials 0.000 claims description 15
- 239000002184 metal Substances 0.000 claims description 15
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 11
- 229930195729 fatty acid Natural products 0.000 claims description 11
- 239000000194 fatty acid Substances 0.000 claims description 11
- 229920002678 cellulose Polymers 0.000 claims description 10
- 239000001913 cellulose Substances 0.000 claims description 10
- 230000000694 effects Effects 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 60
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 27
- 238000012360 testing method Methods 0.000 description 20
- 238000009736 wetting Methods 0.000 description 20
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 18
- 230000008859 change Effects 0.000 description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 15
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 14
- 238000001035 drying Methods 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 10
- 230000032050 esterification Effects 0.000 description 10
- 238000005886 esterification reaction Methods 0.000 description 10
- 244000108321 Diplazium esculentum Species 0.000 description 8
- 235000014276 Diplazium esculentum Nutrition 0.000 description 8
- 244000010375 Talinum crassifolium Species 0.000 description 8
- 235000015055 Talinum crassifolium Nutrition 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- 229920001131 Pulp (paper) Polymers 0.000 description 7
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 7
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000523 sample Substances 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 5
- 125000002252 acyl group Chemical group 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000004513 sizing Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 229960000583 acetic acid Drugs 0.000 description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
- 238000003490 calendering Methods 0.000 description 4
- 239000011436 cob Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000012362 glacial acetic acid Substances 0.000 description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
- 229910052753 mercury Inorganic materials 0.000 description 4
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- -1 alkoxy acetic anhydride Chemical compound 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000011122 softwood Substances 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- 230000010933 acylation Effects 0.000 description 2
- 238000005917 acylation reaction Methods 0.000 description 2
- 230000009172 bursting Effects 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000010981 drying operation Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011121 hardwood Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 238000007788 roughening Methods 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 239000011592 zinc chloride Substances 0.000 description 2
- 235000005074 zinc chloride Nutrition 0.000 description 2
- PNVPNXKRAUBJGW-UHFFFAOYSA-N (2-chloroacetyl) 2-chloroacetate Chemical compound ClCC(=O)OC(=O)CCl PNVPNXKRAUBJGW-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000000397 acetylating effect Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- YHASWHZGWUONAO-UHFFFAOYSA-N butanoyl butanoate Chemical compound CCCC(=O)OC(=O)CCC YHASWHZGWUONAO-UHFFFAOYSA-N 0.000 description 1
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 125000005313 fatty acid group Chemical group 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- LSACYLWPPQLVSM-UHFFFAOYSA-N isobutyric acid anhydride Chemical compound CC(C)C(=O)OC(=O)C(C)C LSACYLWPPQLVSM-UHFFFAOYSA-N 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- RWMKSKOZLCXHOK-UHFFFAOYSA-M potassium;butanoate Chemical compound [K+].CCCC([O-])=O RWMKSKOZLCXHOK-UHFFFAOYSA-M 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002352 surface water Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/775—Photosensitive materials characterised by the base or auxiliary layers the base being of paper
-
- 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
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/14—Carboxylic acids; Derivatives thereof
Definitions
- sizing materials have been applied to the paper either as engine sizing, in the form of tub sizing, or as an application to the surface of the paper.
- Some of the materials which have been employed in this connection are stearic acid, starch, gelatin, rosin, latices and also melamine-formaldehyde and urea-formaldehyde synthetic materials. 'Ihose applications to the paper have helped to some extent but nevertheless there has been considerable room for improvement in the properties of the resulting product.
- a still further object of our invention is to provide a method of making paper base of high wet strength Without the necessity of using formaldehyde-forming resins which heretofore have been considered desirable in the making of high wet strength paper but which may be undesirable for other reasons. Other objects of our invention will appear herein.
- the paper of our invention exhibits properties superior to regular paper in many respects. For instance, the paper of our invention exhibits a dimensional change of less than 1% laterally when that paper is subjected to a wetting with Water for two minutes in a Schopper expansion tester. The paper of our invention exhibits a shrinkage of less than 1% laterally when that paper is soaked in water, dried and then reconditioned. It exhibits a change of less than 15% in a vertical direction upon wetting, and wetting, drying and reconditioning showed a change of less than 5%. Its water absorption by a oneminute Cobb size test is less than .15 gram per 100 I square centimeters.
- the paper of our invention when subjected to the Valley size penetration test exceeds 2,000 seconds, the maximum value to which that test was carried.
- This paper exhibits a rigidty when soaked in water at least twice that of the original waterleaf paper as measured upon a Taber V-S stiffness tester.
- the dry rigidity of this paper is greater than that of the original waterleaf paper especially in the cross direction.
- Papers which have been previously made from high alpha cellulose pulps such as are used for the better and more stable grades of paper employed for photographic purposes show some decrease in brightness when treated in ultraviolet light.
- papers made with lower alpha cellulose pulps heretofore have decreased appreciably in brightness when exposed toultraviolet light
- those made in accordance with our invention from lower alpha cellulose pulps (such as having an alpha cellulose content of -88%) have been found to experience no decrease of brightness after exposure to ultraviolet light of comparable intensities and exposure times.
- Paper in accordance with our invention is prepared by the esterification of paper in sheet form to impart an acyl content of 10-30% thereto.
- This esterification can be accomplished by treating the paper with a process which imparts lower fatty acid radicals to the cellulose of the paper which process would include the use of a bath comprising a lower fatty acid anhydride and an esterification catalyst which bath preferably also contains a solvent.
- the lower fatty acid anhydride may be acetic anhydride, propionic anhydride, butyric anhydride or isobutyric anhydride or the esterification mixture may be made up of a lower fatty acid such as acetic, propionic or butyric acid and an impelling anhydride such as chloracetic anhydride or an alkoxy acetic anhydride.
- the esterification catalyst employed may be perchloric acid,
- the esterification of the paper sheet may be carried out in any one of various ways such as by immersing it in the esterification bath for the time necessary to impart the desired acyl content at the temperature which is employed.
- the paper sheet is conveniently first treated with a pretreatment liquid to swell the cellulose making it more susceptible to the action of the acid anhydride thereon.
- the preferred method of preparing acylated paper is to subject the paper to a pull-through of the materials which act thereon.
- the paper for example, would be subjected to a pull-through of water and the water would be removed from the sheet such as by a pull-through of a lower fatty acid.
- the paper sheet may then be subjected to a pull-through of an esterification bath in which an acid anhydride may cause the chemical combination of the cellulose of the paper sheet with lower fatty acid groups.
- paper sheet having a content of acyl therein within the range of -30% and preferably within the range of -20% of acetyl, propionyl, butyryl or isobutyryl.
- a content of acyl therein within the range of -30% and preferably within the range of -20% of acetyl, propionyl, butyryl or isobutyryl.
- the paper After the paper has been acylated, it may be submitted to pressure drying as the paper comes from the washing operation subsequent to the acylation or it may be dried in a conventional manner, rewetted and then subjected to the pressure drying operation.
- the acylated paper which is treated should contain a liquid such as water or acetone in the amount of at least 12% such as 12-50% of the paper mass.
- the paper obtained from the acylation after Washing free of the materials employed in that operation will ordinarily have a high water content and can be employed directly in the pressure drying operation.
- a liquid content should be imparted thereto such as by soaking in water-miscible liquid such as water, acetone, alcohol or the like, or spraying the paper with liquid in the desired amount.
- the paper in this condition is then subjected to heat and pressure while at least one surface of the paper is in contact with a polished metal surface.
- This operation can be conducted by passing the paper between polished metal rolls or over a polished metal roll having a pressure roll bearing thereon or the paper can be subjected to pressure with a flat polished metal surface which has been polished.
- the temperature employed should be at least 200 F. and preferably 300 F. or more at a mechanical pressure from 300 to 1,000 or more p.s.i.
- the paper is reduced to a moisture content of not more than 5% by this treatment. Ordinarily when heated metal rolls are employed, more than one passage is desirable for the purpose of reducing the moisture content to 5% or less.
- the paper obtained has resistance to the effects of moisture and has a permanently smooth surface, thus giving a product having characteristics advantageous for various usages.
- the paper obtained by the procedure described herein may, if desired, be coated with various aqueous coating compositions such as clay colors or like coating compositions.
- various aqueous coating compositions such as clay colors or like coating compositions.
- the resulting product has a smoothness and glossiness which is retained.
- Paper in accordance with our invention exhibits a dry stiffness greater than that of the original waterleaf paper from which it was prepared, especially in the cross direction. This value is determined on a Taber V-S stifiness tester, as supplied by the Taber Instrument Corporation, North Tonawanda, New York. This test is described in Instrumentation Study No. 14 of the Institute of Paper Chemistry, dated May 27, 1937. In the results recorded of these tests L designates the values obtained in the machine direction and C the values obtained in the cross direction of the paper.
- Paper prepared in accordance with our invention ex hibits a wet stiffness which is at least twice that of the waterleaf paper from which it was prepared.
- the Wet stiffness of paper is determined by soaking the paper samples for three minutes in Water at 7375 F. and then determining the stiffness values on the Taber V-5 stiffness tester using the sensitive 0-10 range.
- the dimensional change, in water, of paper prepared in accordance with our invention is less than 1% laterally in the two-minute test, determined by means of a Schopper expansion tester.
- a strip of paper six inches by fifteen millimeters is cut from the crossdirection of the paper used.
- This sample is fastened by the clamps of that device using care that it is not put under tension or buckled.
- the sample is then immersed in a jar of water for two minutes at the end of which time the scale reading is noted.
- the scale reading gives the wet expansion in percent.
- Paper in accordance with our invention exhibits a shrinkage of less than 1% laterally. This value is determined after first conditioning the paper in an atmosphere of 50% relative humidity. There is then marked off on the paper a given length. The paper is then soaked in water and then dried. The paper is reconditioned at 50% relative humidity. The length on the sample which has been marked off is then measured and the percent of shrinkage can be obtained therefrom.
- the paper in accordance with our invention exhibits a change when wetted of less than 15% in the vertical direction. This value is obtained by using a caliper on the the paper following which the paper is soaked thoroughly in water and a caliper reading is again taken. The difference in the two caliper readings indicates the change in the vertical direction of the paper upon wetting. When the paper is redried the difference in caliper readings indicates a change of less than 5% from the original.
- the water absorption of paper in accordance with our invention by the one-minute Cobb size test is less than .15 gram per 100 square centimeters.
- water is allowed to contact a fixed area of paper for a definite time and the amount absorbed is determined by the gain in weight of the sample (see TAPPI method T441m).
- TAPPI method T441m When paper according to our invention is tested in the Valley penetration test, the value obtained exceeds 2,000 seconds which is the maximum reading taken in that test.
- the testing instrument used was the Valley size tester and in these tests a two-inch square sample of the paper is placed between the two cells of the machine. The set screws are tightened up, the lever at the back is raised and the time is checked by means of a time clock. The results are recorded as the number of seconds taken for the current to reach the required number of milliamperes.
- the solution used in the Valley size tester is as follows:
- Paper in accordance with our invention also exhibits resistance to roughening upon wetting of that paper and drying.
- this paper is wet and dried and the resulting paper is tested in a Surfindicator as made by the Brush Electronics Company, Cleveland, Ohio
- the roughness of the paper does not exceed 85 microinches which constitutes a considerable improvement over papers which have previously been prepared for use in situations where wetting may occur.
- a paper in accordance with our invention will after wetting and redrying give a test on the Surfindicator of no greater than 85 microinches of roughness
- a good standard grade of paper will exhibit a roughness of 120 or more microinches.
- Paper in accordance with. our invention having high initial brightness when wetted, redried and then tested with a Gardner gloss meter exhibits at least 25 reflectance units.
- paper, in accordance with our invention retains its gloss even though subjected to the effects of water.
- Example 1 The paper employed was made from wood pulp consisting of 50 percent hard wood sulfite pulp and 50 percent of soft wood pulp. The pulp was dispersed in water and was adjusted in the paper-making process with aluminum chloride to an acidity of 3-5 milliequivalents per liter. Three percent melamine-formaldehyde resin (based on cellulose) was added to the pulp mass to impart wet strength. Paper was prepared therefrom by coating out on the wire in a conventional paper-making machine, following which the paper was dried on steam heated drums. Sheets of the paper (8" x were acetylated by the following procedure:
- the sheets were pretreated by pulling through the paper 500 ml. of water, then 500 ml. of glacial acetic acid and finally 500 ml. of acetic anhydride containing 5 percent phosphoric acid.
- the temperature of the reagents used was 73 F. and the contact times used in each pull-through operation was -20 seconds using a vacuum of 2.1 cm. of mercury.
- the sheets were then removed and placed in a bath consisting of acetic anhydride containing 5 percent of phosphoric acid (85 percent) at a temperature of 73 F. After keeping the sheets for 1 hour in this bath, they were removed and placed in position for a pull-through of the following:
- the hydraulic press used was a 30-ton. press having polished metal contact surfaces.
- the paper is held onto thedrurn by means of a belt using only sufficient pressure toassure contact between the paper and the drum.
- the paper sam ples that were given a final rinse with water were run through wringer rolls to remove excess surface water.
- the acetone rinse samples were not put through the wringer.
- the wet sheets having approximately 30 percent water or acetone were, when the hydraulic press was used, placed between polished chrome plates and were .subjected to 700 p.s.i. at 300 F. for 10 minutes. The pressure was relieved periodically to allow, vaporto ,escape.
- the gloss ratings are based on the intensities of reflected light read in density units (logarithm). The difference between the rating at 25 and 45 is the logarithm of the ratio of specular to diffuse reflection. A difference of 0.02 is considered significant.
- Roughness was measured in microinches with a Surfiindicator. Instrument settings were: range 300 microinches and cutofi 0.030 inch.
- Example 2 The paper used here was paper having a base weight of 25 /2 pounds per 1,000 square feet made from a mixture of several pulps. The pulp suspension was adjusted with aluminum chloride to an acidity of between 3 and 5 milliequivalents per liter. One percent melamine formaldehyde resin (based on dry cellulose) was added to impart wet strength. All the paper sheets were treated as follows:-
- the sheets were then acetylated by pulling through the paper 500 ml. of acetic anhydride containing 5 percent phosphoric acid (85 percent) at a temperature of 230 F. the contact time with the anhydride was 15 to 20 seconds under a vacuum of 2.1 cm. of mercury.
- the pressure drying was the same as described in the preceding example.
- the starting moisture content in each case was approximately 50 percent.
- the paper was pressed for about 10 minutes with relief periodically to permit escape of vapor.
- the sheets obtained were cut in half and were identified as two groups A to G and A to G
- the samples were treated as described in the preceding example and were tested.
- the paper was then pressure dried and was found to be suitable for use in preparing a photographic paper base in accordance with our invention.
- esterification catalysts such as sulfuric acid, phosphoric acid, methane sulfonic acid, zinc chloride or the like may be convenient for use in preparing partially acetylated paper.
- the rate of esterification can be increased by increasing catalyst concentration and/or anhydride content and/ or temperature.
- partially acetylated paper was prepared by placing rolls of paper on a stainless steel support and treating by dipping and agitating in a series of glass cylinders as follows:
- Example 3 Several l0-inch webs of esterified paper which had been esterified by the procedure described in column 8, lines 7-21, supra, were calendered through one nip of a super calender having a highly polished metal surface, at a temperature of greater than 200 F. and at a pressure of greater than 300 p.s.i., the paper initially having a moisture content of 25%. The treatment of the paper was such as to reduce the moisture content thereof to a moisture value of less than 5%.
- the percentages of cross expansion and swelling of the papers in the table are based on the change in those values when the papers are changed from the dry to the wet state.
- the increase in bulk is the increase in caliper between the dry state and, after the paper is wetted, and then dried, the redried state.
- Papers in accordance with our invention are resistant to the effects of ultraviolet light in comparison with regular paper and in some cases the reflectance of the paper after treating with ultraviolet light is even superior to that which the paper had before treatment. This holds true with partially acylated paper as described herein both in the case of paper which has been pressure dried and paper which has been nonpressure dried. The reflectance of the paper in every case was measured with a G.E. spectrophotometer before and after its exposure in an ultraviolet light chamber, this testing of paper being carried out as described supra.
- pressure drying refers to the treatment of partially acylated paper containing at least 12% of water-miscible liquid at an elevated temperature and pressure (at least 200 F. and at least 300 p.s.i.) against a polished metal surface.
- wet-strength paper originally for the preparation of paper in accordance with our invention has been to facilitate handling. Where the paper sheet is supported while wet a straight water-leaf paper having no size of any kind can be used.
- the type of paper used is a choice of the individual operator for convenience in the paper preparation operation. After paper has been treated in accordance with our invention, it possesses high wet strength characteristics.
- Partially acylated paper exhibits good retention of properties under severe climatic conditions. For instance, samples of acetylated paper (about 20% acetyl), high alpha waterleaf paper and good grade paper were placed in trays and were buried in the tropics for 2 weeks under a mixture of leaf mold, top soil and coarse sand (equal parts). The water content of the burying material was maintained at 27-29% and the temperature at 8283 F., the soil temperature surrounding it being 808l F. The pH of the burying material was 6.9.
- Paper having a lower fatty acid radical content of 10-30% chemically combined therewith which paper wet with at least 12% of water-miscible liquid has been simultaneously pressed at 3001,000 p.s.i. in contact with a polished metal surface and dried at a nondeteriorating temperature of at least 200 F. to a liquid content of not more than 5% and has the following characteristics:
- Paper having a lower fatty acid radical content of 30% chemically combined therewith prepared from wood pulp having an u-cellulose content of at least 85% which paper wet with at least 12% of water-miscible liquid has been simultaneously pressed at 3001,000 p.s.i. in contact with a polished metal surface and dried at a nondeteriorating temperature of at least 200 F. to a liquid content of no more than 5% and has the following characteristics:
- a method of preparing paper having substantially permanent surface characteristics and good resistance to the effects of moisture which comprises the steps of partially acylating the cellulose of the paper so as to impart thereto a 1030% content of lower fatty acid radicals chemically combined therewith and subjecting the paper in a condition wet with a water-miscible liquid in the amount of at least 12% simultaneously to heat and pressing between two solid surfaces at least one of which is a polished metal surface at 300 to 1,000 p.s.i. and a non-deteriorating temperature of at least 200 F. to reduce the liquid content of the paper to a value not more than 5%.
- a method of preparing a paper having substantially permanent surface characteristics and good resistance to the effects of moisture which comprises acetylating the paper to impart thereto an acetyl content of at least 15-20% chemically combined therewith and subjecting the partially acetylated paper while wet with a watermiscible liquid to the amount of at least 12% simultaneously to heat and pressing between two solid surfaces at least one of which is a polished metal surface at 300 to 1,000 p.s.i. and a nondeteriorating temperature of at least 200 F. until the liquid content of the paper has been reduced to a value of not more than 5%.
- a method of preparing a paper having substantially permanent surface characteristics and good resistance to the effects of moisture which comprises acylating cellulose paper to impart thereto a content of 10-30% of fatty acid radicals of 24 carbon atoms chemically combined therewith and subjecting the partially esterified paper with a water content of at least 12% simultaneously to a pressing at 3001,000 p.s.i between two solid surfaces at least one of which is a polished metal surface and a temperature of at least 200 F. to reduce the water content of the paper to not more than 5%.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Paper (AREA)
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE563841D BE563841A (en, 2012) | 1956-04-26 | ||
BE563842D BE563842A (en, 2012) | 1956-04-26 | ||
US580722A US3015537A (en) | 1956-04-26 | 1956-04-26 | Paper having improved characteristics and its preparation |
FR737340A FR1267112A (fr) | 1956-04-26 | 1957-04-26 | Nouveau papier, procédé pour sa fabrication et ses applications notamment en photographie |
FR737339A FR1267111A (fr) | 1956-04-26 | 1957-04-26 | Nouveau papier photographique et procédé pour sa préparation |
DEE14046A DE1082117B (de) | 1956-04-26 | 1957-04-26 | Photographisches Rohpapier und Verfahren zu seiner Herstellung |
GB13470/57A GB858060A (en) | 1956-04-26 | 1957-04-26 | Modified paper, particularly useful in photography, and method of modifying paper |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US580722A US3015537A (en) | 1956-04-26 | 1956-04-26 | Paper having improved characteristics and its preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
US3015537A true US3015537A (en) | 1962-01-02 |
Family
ID=24322266
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US580722A Expired - Lifetime US3015537A (en) | 1956-04-26 | 1956-04-26 | Paper having improved characteristics and its preparation |
Country Status (4)
Country | Link |
---|---|
US (1) | US3015537A (en, 2012) |
BE (2) | BE563842A (en, 2012) |
DE (1) | DE1082117B (en, 2012) |
GB (1) | GB858060A (en, 2012) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3096231A (en) * | 1960-04-18 | 1963-07-02 | Eastman Kodak Co | Method of manufacturing paper from partially esterified cellulose fibers |
US3132944A (en) * | 1960-04-18 | 1964-05-12 | Eastman Kodak Co | Photographic paper prepared from partially acylated cellulose fibers |
US4385172A (en) * | 1980-03-24 | 1983-05-24 | International Paper Company | Prevention of hornification of dissolving pulp |
US4871642A (en) * | 1986-08-04 | 1989-10-03 | Fuji Photo Film Co., Ltd. | Light-sensitive material comprising light-sensitive layer provided on a support comprising a water resistant coating layer |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US585452A (en) * | 1897-06-29 | Wilhelm schroter | ||
GB190325390A (en) * | 1903-11-21 | 1904-02-04 | Ignaz Hoffsuemmer | A Process for Preparing Photographic Printing Paper or the like. |
US1840399A (en) * | 1929-03-01 | 1932-01-12 | Eastman Kodak Co | Sized paper and method of making same |
GB494253A (en) * | 1937-04-23 | 1938-10-24 | Standard Telephones Cables Ltd | Improvements in or relating to the esterification of paper |
GB535932A (en) * | 1939-08-11 | 1941-04-28 | Percy May | Process for the manufacture of laminated strips of cellulose ester fibres |
US2346008A (en) * | 1940-07-27 | 1944-04-04 | Eastman Kodak Co | Manufacture of paper for photographic purposes |
US2348001A (en) * | 1941-10-24 | 1944-05-02 | Nat Vulcanized Fibre Company | Acetylation of cellulose |
US2366723A (en) * | 1941-02-13 | 1945-01-09 | Eastman Kodak Co | Baryta coating of melt-coated paper |
US2379026A (en) * | 1941-07-07 | 1945-06-26 | British Celanese | Treatment of textile and other materials |
US2415631A (en) * | 1945-03-30 | 1947-02-11 | Eastman Kodak Co | Photographic paper |
US2417995A (en) * | 1944-11-14 | 1947-03-25 | Nasa | Acetylation of lignocellulosic board materials |
US2639212A (en) * | 1950-06-07 | 1953-05-19 | Bestpak Inc | Pan liner |
US2646340A (en) * | 1948-10-01 | 1953-07-21 | Monsanto Chemicals | Process of treating natural cellulose textiles to partially esterify them and then treating with a resin condensation product and products resulting therefrom |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE752308C (de) * | 1938-10-28 | 1952-10-13 | Siemens Schuckertwerke A G | Verfahren zur Verminderung der Wasseraufnahmefaehigkeit von Papier |
DE752630C (de) * | 1941-08-20 | 1953-06-15 | Siemens Schuckertwerke A G | Verfahren zur Herstellung von Papier aus veresterten, insbesondere acetylierten Fasern |
-
0
- BE BE563841D patent/BE563841A/xx unknown
- BE BE563842D patent/BE563842A/xx unknown
-
1956
- 1956-04-26 US US580722A patent/US3015537A/en not_active Expired - Lifetime
-
1957
- 1957-04-26 GB GB13470/57A patent/GB858060A/en not_active Expired
- 1957-04-26 DE DEE14046A patent/DE1082117B/de active Pending
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US585452A (en) * | 1897-06-29 | Wilhelm schroter | ||
GB190325390A (en) * | 1903-11-21 | 1904-02-04 | Ignaz Hoffsuemmer | A Process for Preparing Photographic Printing Paper or the like. |
US1840399A (en) * | 1929-03-01 | 1932-01-12 | Eastman Kodak Co | Sized paper and method of making same |
GB494253A (en) * | 1937-04-23 | 1938-10-24 | Standard Telephones Cables Ltd | Improvements in or relating to the esterification of paper |
GB535932A (en) * | 1939-08-11 | 1941-04-28 | Percy May | Process for the manufacture of laminated strips of cellulose ester fibres |
US2346008A (en) * | 1940-07-27 | 1944-04-04 | Eastman Kodak Co | Manufacture of paper for photographic purposes |
US2366723A (en) * | 1941-02-13 | 1945-01-09 | Eastman Kodak Co | Baryta coating of melt-coated paper |
US2379026A (en) * | 1941-07-07 | 1945-06-26 | British Celanese | Treatment of textile and other materials |
US2348001A (en) * | 1941-10-24 | 1944-05-02 | Nat Vulcanized Fibre Company | Acetylation of cellulose |
US2417995A (en) * | 1944-11-14 | 1947-03-25 | Nasa | Acetylation of lignocellulosic board materials |
US2415631A (en) * | 1945-03-30 | 1947-02-11 | Eastman Kodak Co | Photographic paper |
US2646340A (en) * | 1948-10-01 | 1953-07-21 | Monsanto Chemicals | Process of treating natural cellulose textiles to partially esterify them and then treating with a resin condensation product and products resulting therefrom |
US2639212A (en) * | 1950-06-07 | 1953-05-19 | Bestpak Inc | Pan liner |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3096231A (en) * | 1960-04-18 | 1963-07-02 | Eastman Kodak Co | Method of manufacturing paper from partially esterified cellulose fibers |
US3132944A (en) * | 1960-04-18 | 1964-05-12 | Eastman Kodak Co | Photographic paper prepared from partially acylated cellulose fibers |
US4385172A (en) * | 1980-03-24 | 1983-05-24 | International Paper Company | Prevention of hornification of dissolving pulp |
US4871642A (en) * | 1986-08-04 | 1989-10-03 | Fuji Photo Film Co., Ltd. | Light-sensitive material comprising light-sensitive layer provided on a support comprising a water resistant coating layer |
Also Published As
Publication number | Publication date |
---|---|
BE563842A (en, 2012) | |
DE1082117B (de) | 1960-05-19 |
GB858060A (en) | 1961-01-04 |
BE563841A (en, 2012) |
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