US2963395A - Process of bleaching lignocellulosic pulps - Google Patents
Process of bleaching lignocellulosic pulps Download PDFInfo
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- US2963395A US2963395A US724944A US72494458A US2963395A US 2963395 A US2963395 A US 2963395A US 724944 A US724944 A US 724944A US 72494458 A US72494458 A US 72494458A US 2963395 A US2963395 A US 2963395A
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- Prior art keywords
- pulp
- hydrosulfite
- bleaching
- weight
- brightness
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- 238000004061 bleaching Methods 0.000 title claims description 52
- 238000000034 method Methods 0.000 title description 29
- 230000008569 process Effects 0.000 title description 24
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 claims description 47
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 20
- 239000001301 oxygen Substances 0.000 claims description 20
- 229910052760 oxygen Inorganic materials 0.000 claims description 20
- 239000007844 bleaching agent Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 11
- 229910052783 alkali metal Inorganic materials 0.000 claims description 8
- 239000007864 aqueous solution Substances 0.000 claims description 8
- 238000009895 reductive bleaching Methods 0.000 claims description 7
- 150000001340 alkali metals Chemical class 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- 239000011701 zinc Substances 0.000 claims description 3
- 238000010924 continuous production Methods 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 239000000243 solution Substances 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000003381 stabilizer Substances 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 6
- PENRVBJTRIYHOA-UHFFFAOYSA-L zinc dithionite Chemical compound [Zn+2].[O-]S(=O)S([O-])=O PENRVBJTRIYHOA-UHFFFAOYSA-L 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000010926 purge Methods 0.000 description 5
- 235000019832 sodium triphosphate Nutrition 0.000 description 4
- 229920000388 Polyphosphate Polymers 0.000 description 3
- 229920001131 Pulp (paper) Polymers 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- -1 alkali metal hydrosulfites Chemical class 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 230000009969 flowable effect Effects 0.000 description 3
- 239000001205 polyphosphate Substances 0.000 description 3
- 235000011176 polyphosphates Nutrition 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 240000002317 Camassia leichtlinii Species 0.000 description 2
- 235000000459 Camassia leichtlinii Nutrition 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 241000287127 Passeridae Species 0.000 description 2
- FCMYSEXCLRFWBP-UHFFFAOYSA-N [NH4+].[NH4+].[O-]S(=O)S([O-])=O Chemical class [NH4+].[NH4+].[O-]S(=O)S([O-])=O FCMYSEXCLRFWBP-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 230000006735 deficit Effects 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 229960001484 edetic acid Drugs 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000004537 pulping Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000009827 uniform distribution Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 240000003021 Tsuga heterophylla Species 0.000 description 1
- 235000008554 Tsuga heterophylla Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- ZETCGWYACBNPIH-UHFFFAOYSA-N azane;sulfurous acid Chemical compound N.OS(O)=O ZETCGWYACBNPIH-UHFFFAOYSA-N 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 238000004182 chemical digestion Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical class OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- TVHALOSDPLTTSR-UHFFFAOYSA-H hexasodium;[oxido-[oxido(phosphonatooxy)phosphoryl]oxyphosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O TVHALOSDPLTTSR-UHFFFAOYSA-H 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000012978 lignocellulosic material Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- HEZHYQDYRPUXNJ-UHFFFAOYSA-L potassium dithionite Chemical compound [K+].[K+].[O-]S(=O)S([O-])=O HEZHYQDYRPUXNJ-UHFFFAOYSA-L 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 239000002562 thickening agent 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
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/1005—Pretreatment of the pulp, e.g. degassing the pulp
-
- 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
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/1084—Bleaching ; Apparatus therefor with reducing compounds
- D21C9/1089—Bleaching ; Apparatus therefor with reducing compounds with dithionites
Definitions
- This invention relates to a process of bleaching lignocellulosic pulps. More specifically, it relates to bleaching fibrous lignocellulosic pulps using a water-soluble hydro: sulfite as the essential bleaching agent.
- Aqueous pulp suspensions having a relatively low dry fiber content contain a large amount of water and consequently require large size bleaching equipment, require a relatively long bleaching time to attain a high degree of brightness, consume large quantities of heat, have a tendency of contaminating pulp with undesirable ions generally present in water, and produce a considerable quantity of efiluent from the bleaching operation which contributes to the stream pollution.
- Still another object of this invention is to provide an improved process of bleaching pulps at high consistency with a reducing bleaching agent under controlled operating conditions, whereby pulps of maximum brightness are produced with a highly efiicient use of the hydrosulfite in a relatively short time, while a uniform distribution of the bleaching solution throughout the moist pulp mass is achieved.
- bleached lignocellulosic pulp is produced by first providing a moist mass of pulp having a dry fiber content higher than 15% but not exceeding 50%, by weight, removing a substantial proportion of air from the pulp, admixing the pulp with an aqueous solution comprising essentially a hydrosulfite bleaching agent and a stabilizer therefor, and subjecting the pulp to the action of said bleaching agent in an atmosphere substantially free of oxygen at a temperature between about 100 F. and 230 F., While maintaining the pulp consistency throughout the bleaching in the range of 1550%, and a pH of about 4 to 8 for a period of time sufficient to produce a substantial increase in brightness of said pulp.
- the bleached pulp is discharged from the oxygen- Patented Dec. 6, 1960 free zone. It then may be diluted with water to low consistency normally used in the conversion of pulps to paper.
- the lignocellulosic pulps suitable in the practice of the present invention may comprise mechanical pulps derived from wood or non-woody lignocellulose, semi-chemical pulps, and pulps derived from chemical digestion of wood or other lignocellulosic materials. Such pulps still contain a certain proportion of lignin materials, depending on the pulping procedure employed.
- the pulp coming directly from either mechanical, semichemical or chemical pulping operations is usually of low consistency.
- the pulp consistency must be, therefore, increased to a value of from above 15 to 50% by weight, oven-dry pulp basis.
- This may be efiectuated in any suitable dewatering equipment, such as a vacuum thickener, screwpress and the like.
- the moist, high-consistency pulp is then shredded or otherwise comminuted in particulate form, if necessary, in order to facilitate removal of air therefrom and its subsequent mixing with the bleaching solution.
- the comminuted pulp in form of a semi-solid, discontinuous moist mass, having voids therein and containing an appreciable quantity of air may be carried by any suitable conveying means, such as a screw conveyor, to a mixing chamber.
- a mixing chamber may be equipped with suitable agitating means, such as a double shaft mixer, which is generally satisfactory for pulps having a consistency between 15 and 20%.
- the chamber should be provided with an inlet for steam or gas and withan outlet for purging oxygen therefrom. If an excess of steam is present in the chamber, such excess may bereleased; through such outlet and recovered for heating purposes.
- the pulp mass substantially free of oxygen, may be transferred through an air-tight conduit to another mixing chamber where it is mixed mechanically with the solution of the hydrosulfite bleaching agent.
- the removal of air and the subsequent mixing with the bleaching agent may be carried out in a screw press or in a pulper of refiner-type, such as a roto pulper.
- Good results may be also obtained by first removing air from the pulp in a screw press, feeding the substantially oxygen-free pulp into a pulper into which the bleach solution is incorporated and thoroughly mixed with the pulp.
- the resulting bleached pulp may be discharged onto a screw conveyor and transported thereby to a dilution tank.
- the pulp be confined in an air-tight mixing equipment so as to prevent the access of air from the outside, and thus maintain a substantially oxygen-free atmosphere until the bleaching of the pulp is complete.
- the removal of a substantial proportion of oxygen contained in the moist, comminuted pulp, which constitutes an integral step in the present process, may be carried out by purging with live steam or with inert gases, such as nitrogen, line gas from furnaces operating under reducing conditions, or by means of vacuum.
- the preferred procedure is to inject live steam into the mixing chamber, while subjecting the pulp to vigorous agitation. This produces an atmosphere substantially free of oxygen.
- steam purging may be effectuated countercurrently in a suitable mixing apparatus.
- the lignocellulosic pulp, substantially free of oxygen, is then admixed with a solution of a hydrosulfite which is the essential bleaching agent in accordance with the present invention.
- a hydrosulfite which is the essential bleaching agent in accordance with the present invention.
- suitable water-soluble hydrosulfites are zinc hydrosulfite, the alkali metal hydrosulfites, such as sodium and potassium hydrosulfite, ammonium hydrosulfite, and the like. These may be used singly or in admixture with each other.
- Sodium hydrosulfite and zinc hydrosulfite are the preferred members of the group.
- the aqueous solutions of the hydrosulfite may be prepared at any desired concentration of hydrosulfite depending upon its solubility characteristics.
- a suitable concentration range for a hydrosulfite solution may be from 2 to 10%, by weight, calculated as sodium hydrosulfite, however it is to be understood that higher or lower concentrations may be employed, if desired.
- the amount of a hydrosulfite employed in the bleaching of the lignocellulosic pulps may vary according to the degree of brightness increase desired, as well as de ending on the type of pulp used. In general, from 0.2% to by weight of hydrosulfite, based on the weight of oven-dry pulp will be sutficient to obtain the desired brightness increase. The preferred range for the use of hydrosulfite is from 0.5% to 2% by weight, based on the oven-dry weight of pulp.
- a certain amount of a stabilizer for the hydrosulfite is incorporated in the hydrosulfite solution, or in the pulp prior to its admixture with the bleaching agent.
- suitable stabilizers for hydrosulfite are watersoluble polyphosphates, such as sodium tripolyphosphate, sodium tetraphosphate, sodium pyrophosphate and the like.
- Suitable stabilizers for the hydrosulfite comprise commercially available chelating agents such as ethylene-diamine-tetra-acetic acid or the alkali metal, alkaline earth metal and ammonium salts thereof, alkali metal citrates and the like.
- the amount of the chelating agent employed is generally somewhat lower than that of a polyphosphate-type stabilizer. In general, an amount of from 0.01% to 2%, preferably from 0.05% to 0.5%, by weight, based on the oven-dry weight of the pulp is sutficient. Any of the foregoing types of stabilizers for the hydrosulfite may be used singly or in admixture with each other.
- a freshly prepared aqueous solution of a stabilized hydrosulfite should have a pH value in the neighborhood of neutrality.
- a satisfactory pH range for such solution may range from about 5 to about 12, depending on the type of hydrosulfite employed and the acidity of the pulp to be bleached.
- a small amount of an alkaline material such as sodium hydroxide, sodium carbonate, and the like, may be added into the bleaching solution for adjustment for its pH within the above indicated range.
- the lignocellulosic pulp is treated with the hydrosulfite bleaching agent at a temperature which lies broadly between 100 F. and about 230 F, preferably between 140 F. and 215 F.
- the bleaching treatment is continued for a time sufficient to produce a substantial increase in the pulp brightness.
- the duration of the bleaching treatment is determined by such factors as the bleaching temperature, the amount of bleaching agent employed, the pulp consistency, and the identity of the lignocellulosic pulp. In general, however, a reaction time at a temperature of from 100 F. to 230 F. will be from one minute to about sixty minutes, the longer reaction times being employed with the lower temperatures and vice versa.
- the accompanying drawing is a graph plotting the bleaching time in minutes against the bleaching temperature in degrees Fahrenheit.
- the curves shown represent time required for bleaching groundwood at three pulp consistency levels, namely 2.5%, 4% and 25% by weight, respectively, in an atmosphere substantially oxygen-free, using 1% of sodium hydrosulfite and 0.5% of sodium tripolyphosphate, by weight, each based on the weight of oven-dry pulp.
- the bleaching time, as indicated, was required in each case to increase the original brightness of the pulp from 59% GE to 70% GB, or a brightness increase of 11 points.
- the pulp which has been thickened to a consistency above 15% and not exceeding 50% by weight may be fed continuously by a suitable conveyor means, such as a screw conveyor, to a suitable air-tight mixing chamber mm which oxygen is continuously removed.
- the stabil'zed hydrosulfite solution is then continuously fed into the pulp mass at such a rate as to provide a hydrosulfite usage of (ll-5%, by weight, oven-dry pulp basis, as indicated above.
- the mixture is subjected to a vigorous agitation in order to obtain a thorough mixing of the bleaching solution with the pulp.
- the bleaching reaction is continued in an atmosphere substantially oxygen-free for a short period, as may be necessary to obtain a desired pulp brightness increase.
- the bleached pulp is discharged by dumping or any other suitable means to a dilution tank where it is mixed with water to a consistency level suitable for papermaking operations.
- Example 1 -Gr0undwood pulp derived from west coast softwood species having the brightness of 59% GERS (General Electric Recording Sp.ctrophotometer) is partially dewatered to a consistency of 28.4% and shredded in the form of small particles. It is then placed in a suitable air-tight vessel provided with agitating means. Live steam is injected into the pulp-containing ve sel in order to purge out substantially all of the air therefrom.
- GERS General Electric Recording Sp.ctrophotometer
- the resulting mixture having a consistency of about 25%, and a pH 5.5, is vigorously agitated to insure a substantially uniform distribution of the bleaching agent throughout the pulp mass and maintained in an atmosphere substantially free of oxygen at a temperature of about 212 F. for five minutes. It is next discharged from the vessel, further diluted with water and formed into a sheet.
- the resulting bleached pulp produced by the foregoing procedure has a brightness value of 70% GERS, corresponding to a brightness increase of 11 points.
- Example 2 The same pulp as described in Example 1 is treated in the same manner as in Example 1, except that the pulp consistency during bleaching is 18% and the reaction time is 10 minutes.
- the resulting bleached pulp has a brightness of 70% GERS, or a brightness increase of 11 points.
- Example 3.Groundwood pulp having 58% GE brightness is bleached in an atmosphere substantially free of oxygen obtained by applying a vacuum of about 24 inches or mercury in the reaction vessel.
- the pulp is aoeasss subjected to the action of the same bleaching solution and in the same amount as described in Example 1 for 30 minutes at a temperature of 140 F. at 25% consistency.
- the pH of the pulp mixture is maintained at 6 during bleaching.
- the bleached pulp is discharged, diluted with water and formed into a sheet.
- the resulting pulp has a brightness of 70% GERS, corresponding to a brightness increase of 12 points.
- Example 4 The same pulp as employed in Example 1 is treated in the same manner as described in Example 3 with a reducing bleaching agent consisting of an aqueous solution containing 1% of zinc hydrosulfite and 0.5% of sodium tripolyphosphate by weight.
- the amount of the hydrosulfite added is 1.11%, by weight, based on the oven-dry weight of pulp.
- the pulp is bleached at 25 consistency in an atmosphere substantially free of oxygen for 30 minutes at 140 F
- the resulting bleached pulp has a brightness of 70% GERS, compared to its initial brightness value of 59% GERS. Hence, an increase in brightness of 11 points is achieved.
- Example 5 Unbleached sulfite pulp produced by cooking western hemlock by the conventional acid sulfite process is admixed with the same groundwood pulp as described in Example 1 in the proportion of and 80%, respectively.
- the brightness of the pulp is 60% GERS.
- the pulp at 28% consistency is shredded and placed in a suitable air-tight vessel provided with agitating means. In order to remove air from the vessel, the pulp is heated to 170 F., the pressure is reduced to a value corresponding to the vapor pressure of water at this temperature (a vacuum of about 18 inches of mercury), then nitrogen gas is injected while normal atmospheric pressure is gradually restored in the vessel.
- the same bleaching solution as employed in Example 1 is added to the pulp in amount sufficient to give 1.5% hydrosulfite and 0.75% polyphosphate by weight, based on the weight of oven-dry pulp.
- the bleaching is carried out with continuous agitation in the atmosphere of nitrogen at 170 F. for minutes.
- the consistency of the pulp during bleaching is about 25% and the pH value of 5.5 is maintained throughout the reaction period.
- the brightness of the resulting bleached pulp is 72% GERS, corresponding to a brightness increase of 12 points.
- the continuous process of bleaching lignocellulosic pulp which comprises feeding into an air-tight zone a semi-solid, non-flowable, moist mass of pulp in particulate form, removing substantially all of the air therefrom, forming a mixture containing said pulp and a reducing bleaching agent comprising essentially a stabilized aqueous solution of a hydrosulfite selected from the group consisting of zinc, alkali metal and ammonium hydrosulfites, the amount of said hydrosulfite being from 0.2% to 5%, by weight, oven-dry pulp basis, and mixing mechanically said pulp with said hydrosulfite in an atmosphere substantially free of oxygen at a temperature of from F. to 230 F. for a period of time sufficient to produce a substantial increase in the pulp brightness, the pH of said mixture during bleaching being maintained between about 4 and 8.
- hydrosulfite comprises zinc hydrosulfite.
- hydrosulfite comprises sodium hydrosulfite
- hydrosulfite comprises sodium hydrosulfite
- hydrosulfite comprises zinc hydrosulfite.
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Description
Deg. 6, 1960 5. BACK ETAL 2,963,395
' PROCESS OF BLEACHING LIGNOCELLULOSIC PULPS Filed March 51, 1958 (D B /2.5% PULP CONSISTENCY I) Z o 12 LJ 2 4 Z, PULP 3 CON SISTENCY i 3 so LL PULP CONSISTENCY 60 I 4O i 0 so 100 I20 I I I 200 220 BLEACHING TEMPERATURE, DEG. F. INVENTORS SANGHO BACK DELMER D. HINRICHS JAMES D. WETHERN BY J6.
AENTV PROCESS OF BLEACHING LIGNOCELLULOSIC PULPS Sangho Back, Camas, Delmer D. Hinrichs, Washougal, and James D. Wethern, Camas, Wash., assignors to Crown Zellerbach Corporation, San Francisco, Calif., a corporation of Nevada Filed Mar. 31, 1958, Ser. No. 724,944
15 Claims. (Cl. 16283) This invention relates to a process of bleaching lignocellulosic pulps. More specifically, it relates to bleaching fibrous lignocellulosic pulps using a water-soluble hydro: sulfite as the essential bleaching agent.
The bleaching of wood pulp, particularly groundwood, with either sodium or Zinc hydrosulfite is well known in the pulp and paper industry. The procedures suggested or employed commercially in the industry involve the use of pulp to be bleached in a slush form, usually at a low consistency of from about 0.5% to about 6%. Aqueous pulp suspensions having a relatively low dry fiber content, as indicated above, contain a large amount of water and consequently require large size bleaching equipment, require a relatively long bleaching time to attain a high degree of brightness, consume large quantities of heat, have a tendency of contaminating pulp with undesirable ions generally present in water, and produce a considerable quantity of efiluent from the bleaching operation which contributes to the stream pollution.
Accordingly, it is the general object of the present invention to overcome such disadvantages by providing an improved process of bleaching lignocellulosic pulps with a water-soluble hydrosulfite at a high pulp consistency, i.e. containing an insuflicient amount of water to produce a free-flowing slurry but rather forming a semisolid, non-flowable, moist mass of pulp containing more than 15% by weight of oven-dry fiber.
It is also an object of the invention to provide a process 7 of bleaching pulps with a stabilized water-soluble hydrosulfite at high pulp consistency and in an atmosphere substantially free of oxygen in order to obtain maximum bleaching efiiciency of the hydrosulfite upon the pulp.
Still another object of this invention is to provide an improved process of bleaching pulps at high consistency with a reducing bleaching agent under controlled operating conditions, whereby pulps of maximum brightness are produced with a highly efiicient use of the hydrosulfite in a relatively short time, while a uniform distribution of the bleaching solution throughout the moist pulp mass is achieved.
Other objects and advantages of this invention will be apparent from the following description.
Briefly stated, bleached lignocellulosic pulp according to the present invention is produced by first providing a moist mass of pulp having a dry fiber content higher than 15% but not exceeding 50%, by weight, removing a substantial proportion of air from the pulp, admixing the pulp with an aqueous solution comprising essentially a hydrosulfite bleaching agent and a stabilizer therefor, and subjecting the pulp to the action of said bleaching agent in an atmosphere substantially free of oxygen at a temperature between about 100 F. and 230 F., While maintaining the pulp consistency throughout the bleaching in the range of 1550%, and a pH of about 4 to 8 for a period of time sufficient to produce a substantial increase in brightness of said pulp.
After the desired degree of pulp brightness has been attained, the bleached pulp is discharged from the oxygen- Patented Dec. 6, 1960 free zone. It then may be diluted with water to low consistency normally used in the conversion of pulps to paper.
The lignocellulosic pulps suitable in the practice of the present invention may comprise mechanical pulps derived from wood or non-woody lignocellulose, semi-chemical pulps, and pulps derived from chemical digestion of wood or other lignocellulosic materials. Such pulps still contain a certain proportion of lignin materials, depending on the pulping procedure employed.
The pulp coming directly from either mechanical, semichemical or chemical pulping operations is usually of low consistency. In accordance with the present invention, the pulp consistency must be, therefore, increased to a value of from above 15 to 50% by weight, oven-dry pulp basis. This may be efiectuated in any suitable dewatering equipment, such as a vacuum thickener, screwpress and the like. The moist, high-consistency pulp is then shredded or otherwise comminuted in particulate form, if necessary, in order to facilitate removal of air therefrom and its subsequent mixing with the bleaching solution.
The comminuted pulp in form of a semi-solid, discontinuous moist mass, having voids therein and containing an appreciable quantity of air, may be carried by any suitable conveying means, such as a screw conveyor, to a mixing chamber. Such chamber may be equipped with suitable agitating means, such as a double shaft mixer, which is generally satisfactory for pulps having a consistency between 15 and 20%. The chamber should be provided with an inlet for steam or gas and withan outlet for purging oxygen therefrom. If an excess of steam is present in the chamber, such excess may bereleased; through such outlet and recovered for heating purposes.
The pulp mass, substantially free of oxygen, may be transferred through an air-tight conduit to another mixing chamber where it is mixed mechanically with the solution of the hydrosulfite bleaching agent.
For pulps having a consistency in the range of from about 20% to 50% the removal of air and the subsequent mixing with the bleaching agent may be carried out in a screw press or in a pulper of refiner-type, such as a roto pulper. Good results may be also obtained by first removing air from the pulp in a screw press, feeding the substantially oxygen-free pulp into a pulper into which the bleach solution is incorporated and thoroughly mixed with the pulp. The resulting bleached pulp may be discharged onto a screw conveyor and transported thereby to a dilution tank.
It is important that after oxygen has been removed from the pulp, the pulp be confined in an air-tight mixing equipment so as to prevent the access of air from the outside, and thus maintain a substantially oxygen-free atmosphere until the bleaching of the pulp is complete.
The removal of a substantial proportion of oxygen contained in the moist, comminuted pulp, which constitutes an integral step in the present process, may be carried out by purging with live steam or with inert gases, such as nitrogen, line gas from furnaces operating under reducing conditions, or by means of vacuum. The preferred procedure is to inject live steam into the mixing chamber, while subjecting the pulp to vigorous agitation. This produces an atmosphere substantially free of oxygen. If desired, steam purging may be effectuated countercurrently in a suitable mixing apparatus.
The lignocellulosic pulp, substantially free of oxygen, is then admixed with a solution of a hydrosulfite which is the essential bleaching agent in accordance with the present invention. Examples of suitable water-soluble hydrosulfites are zinc hydrosulfite, the alkali metal hydrosulfites, such as sodium and potassium hydrosulfite, ammonium hydrosulfite, and the like. These may be used singly or in admixture with each other. Sodium hydrosulfite and zinc hydrosulfite are the preferred members of the group. The aqueous solutions of the hydrosulfite may be prepared at any desired concentration of hydrosulfite depending upon its solubility characteristics. A suitable concentration range for a hydrosulfite solution may be from 2 to 10%, by weight, calculated as sodium hydrosulfite, however it is to be understood that higher or lower concentrations may be employed, if desired. In preparing the hydrosulfite aqueous solution it may be desirable to pretreat the water employed by deaerating it so that incorporation of oxygen into the pulp mixture during bleaching will be reduced to a minimum.
The amount of a hydrosulfite employed in the bleaching of the lignocellulosic pulps may vary according to the degree of brightness increase desired, as well as de ending on the type of pulp used. In general, from 0.2% to by weight of hydrosulfite, based on the weight of oven-dry pulp will be sutficient to obtain the desired brightness increase. The preferred range for the use of hydrosulfite is from 0.5% to 2% by weight, based on the oven-dry weight of pulp.
In order to improve the stability of a hydrosulfite in an aqueous solution and to avoid impairment of bleaching response due to possible contamination of pulp with certain metal ions, such as iron, copper, manganese and the like which may be present in the pulp itself or in the Water, a certain amount of a stabilizer for the hydrosulfite is incorporated in the hydrosulfite solution, or in the pulp prior to its admixture with the bleaching agent. Examples of suitable stabilizers for hydrosulfite are watersoluble polyphosphates, such as sodium tripolyphosphate, sodium tetraphosphate, sodium pyrophosphate and the like. Other suitable stabilizers for the hydrosulfite comprise commercially available chelating agents such as ethylene-diamine-tetra-acetic acid or the alkali metal, alkaline earth metal and ammonium salts thereof, alkali metal citrates and the like. The amount of the chelating agent employed is generally somewhat lower than that of a polyphosphate-type stabilizer. In general, an amount of from 0.01% to 2%, preferably from 0.05% to 0.5%, by weight, based on the oven-dry weight of the pulp is sutficient. Any of the foregoing types of stabilizers for the hydrosulfite may be used singly or in admixture with each other.
A freshly prepared aqueous solution of a stabilized hydrosulfite should have a pH value in the neighborhood of neutrality. A satisfactory pH range for such solution may range from about 5 to about 12, depending on the type of hydrosulfite employed and the acidity of the pulp to be bleached. If necessary, a small amount of an alkaline material, such as sodium hydroxide, sodium carbonate, and the like, may be added into the bleaching solution for adjustment for its pH within the above indicated range. After the hydrosulfite containing solution having a pH within the above stipulated range has been added to and mixed with the pulp to be bleached in an atmosphere substantially free of oxygen, the pH of the mixture during bleaching is maintained at a value between about 4 and 8, preferably between about 5 and 7.
The lignocellulosic pulp is treated with the hydrosulfite bleaching agent at a temperature which lies broadly between 100 F. and about 230 F, preferably between 140 F. and 215 F. The bleaching treatment is continued for a time sufficient to produce a substantial increase in the pulp brightness.
The duration of the bleaching treatment is determined by such factors as the bleaching temperature, the amount of bleaching agent employed, the pulp consistency, and the identity of the lignocellulosic pulp. In general, however, a reaction time at a temperature of from 100 F. to 230 F. will be from one minute to about sixty minutes, the longer reaction times being employed with the lower temperatures and vice versa.
The accompanying drawing is a graph plotting the bleaching time in minutes against the bleaching temperature in degrees Fahrenheit. The curves shown represent time required for bleaching groundwood at three pulp consistency levels, namely 2.5%, 4% and 25% by weight, respectively, in an atmosphere substantially oxygen-free, using 1% of sodium hydrosulfite and 0.5% of sodium tripolyphosphate, by weight, each based on the weight of oven-dry pulp. The bleaching time, as indicated, was required in each case to increase the original brightness of the pulp from 59% GE to 70% GB, or a brightness increase of 11 points.
As is apparent from the drawing, a considerable reduction in bleaching time at a given temperature level, this being accompanied by other advantages, as explained hereinabove, can be realized by hydrosulfite bleaching of pulp at high consistency.
Although a batch process may be used for bleaching the lignocellulosic pulp in accordance with the present invention, it is preferred in commercial practice to carry out this operation continuously. Thus, the pulp which has been thickened to a consistency above 15% and not exceeding 50% by weight may be fed continuously by a suitable conveyor means, such as a screw conveyor, to a suitable air-tight mixing chamber mm which oxygen is continuously removed. The stabil'zed hydrosulfite solution is then continuously fed into the pulp mass at such a rate as to provide a hydrosulfite usage of (ll-5%, by weight, oven-dry pulp basis, as indicated above. The mixture is subjected to a vigorous agitation in order to obtain a thorough mixing of the bleaching solution with the pulp. The bleaching reaction is continued in an atmosphere substantially oxygen-free for a short period, as may be necessary to obtain a desired pulp brightness increase. The bleached pulp is discharged by dumping or any other suitable means to a dilution tank where it is mixed with water to a consistency level suitable for papermaking operations.
The present invention is further illustrated by the following specific examples which are not intended to limit the scope thereof.
Example 1.-Gr0undwood pulp derived from west coast softwood species having the brightness of 59% GERS (General Electric Recording Sp.ctrophotometer) is partially dewatered to a consistency of 28.4% and shredded in the form of small particles. It is then placed in a suitable air-tight vessel provided with agitating means. Live steam is injected into the pulp-containing ve sel in order to purge out substantially all of the air therefrom. An aqueous bleaching solution containing 2% by weight of sodium hydrosulfite, 1% by weight of sodium tripolyphosphate and 0.16% by weight of sodium hydroxide, is added to the deaerated pulp in an amount sufiicient to provide 1% by weight of hydrosulfite, based on the weight of oven-dry pulp. The resulting mixture, having a consistency of about 25%, and a pH 5.5, is vigorously agitated to insure a substantially uniform distribution of the bleaching agent throughout the pulp mass and maintained in an atmosphere substantially free of oxygen at a temperature of about 212 F. for five minutes. It is next discharged from the vessel, further diluted with water and formed into a sheet. The resulting bleached pulp produced by the foregoing procedure has a brightness value of 70% GERS, corresponding to a brightness increase of 11 points.
Example 2.The same pulp as described in Example 1 is treated in the same manner as in Example 1, except that the pulp consistency during bleaching is 18% and the reaction time is 10 minutes. The resulting bleached pulp has a brightness of 70% GERS, or a brightness increase of 11 points.
Example 3.Groundwood pulp having 58% GE brightness is bleached in an atmosphere substantially free of oxygen obtained by applying a vacuum of about 24 inches or mercury in the reaction vessel. The pulp is aoeasss subjected to the action of the same bleaching solution and in the same amount as described in Example 1 for 30 minutes at a temperature of 140 F. at 25% consistency. The pH of the pulp mixture is maintained at 6 during bleaching. At the end of this reaction period the bleached pulp is discharged, diluted with water and formed into a sheet. The resulting pulp has a brightness of 70% GERS, corresponding to a brightness increase of 12 points.
Example 4.--The same pulp as employed in Example 1 is treated in the same manner as described in Example 3 with a reducing bleaching agent consisting of an aqueous solution containing 1% of zinc hydrosulfite and 0.5% of sodium tripolyphosphate by weight. The amount of the hydrosulfite added is 1.11%, by weight, based on the oven-dry weight of pulp. The pulp is bleached at 25 consistency in an atmosphere substantially free of oxygen for 30 minutes at 140 F The resulting bleached pulp has a brightness of 70% GERS, compared to its initial brightness value of 59% GERS. Hence, an increase in brightness of 11 points is achieved.
Example 5.Unbleached sulfite pulp produced by cooking western hemlock by the conventional acid sulfite process is admixed with the same groundwood pulp as described in Example 1 in the proportion of and 80%, respectively. The brightness of the pulp is 60% GERS. The pulp at 28% consistency is shredded and placed in a suitable air-tight vessel provided with agitating means. In order to remove air from the vessel, the pulp is heated to 170 F., the pressure is reduced to a value corresponding to the vapor pressure of water at this temperature (a vacuum of about 18 inches of mercury), then nitrogen gas is injected while normal atmospheric pressure is gradually restored in the vessel. The same bleaching solution as employed in Example 1 is added to the pulp in amount sufficient to give 1.5% hydrosulfite and 0.75% polyphosphate by weight, based on the weight of oven-dry pulp. The bleaching is carried out with continuous agitation in the atmosphere of nitrogen at 170 F. for minutes. The consistency of the pulp during bleaching is about 25% and the pH value of 5.5 is maintained throughout the reaction period. The brightness of the resulting bleached pulp is 72% GERS, corresponding to a brightness increase of 12 points.
It will be apparent that by'the practice of the present invention we have provided an improved process for the manufacture of high quality lignocellulosic pulps, particularly groundwood, or high degree of brightness which process includes bleaching high consistency pulp in form of a non-flowable, semi-solid mass, incapable of forming a continuous stream upon pouring, in an atmosphere substantially free of oxygen using a stabilized, watersoluble hydrosulfite as the essential bleaching agent. It will be also apparent that the bleaching procedure with a hydrosulfite at high consistencies in accordance with the present invention, presents several advantages over that conventionally practiced in the pulp industry wherein low-consistency, flowing streams of slush pulps are employed. These advantages include a more eflicient use of the reducing bleaching agent, a considerable reduction in bleaching time, heat economy, use of small size equipment, and reduction of stream pollution due to a smaller volume of eflduent produced. The foregoing and other advantages can be achieved without any impairment of other physical or chemical properties of the resulting bleached pulps.
Having thus described our invention in preferred embodiments, we claim:
1. The continuous process of bleaching lignocellulosic pulp which comprises feeding into an air-tight zone a semi-solid, non-flowable, moist mass of pulp in particulate form, removing substantially all of the air therefrom, forming a mixture containing said pulp and a reducing bleaching agent comprising essentially a stabilized aqueous solution of a hydrosulfite selected from the group consisting of zinc, alkali metal and ammonium hydrosulfites, the amount of said hydrosulfite being from 0.2% to 5%, by weight, oven-dry pulp basis, and mixing mechanically said pulp with said hydrosulfite in an atmosphere substantially free of oxygen at a temperature of from F. to 230 F. for a period of time sufficient to produce a substantial increase in the pulp brightness, the pH of said mixture during bleaching being maintained between about 4 and 8.
2. The process of claim 1 wherein the pH of the mixture is maintained between about 5 and 7.
3. The process of claim 1 wherein air is removed from the pulp by purging with live steam and the pulp is bleached at a temperature of about 212 F.
4. The process of claim 1 wherein the hydrosulfite comprises zinc hydrosulfite.
5. The process of claim 1 wherein the hydrosulfite comprises sodium hydrosulfite.
6. The process of claim 1 wherein the amount of the hydrosulfite employed is from 0.5% to 2% by weight.
7. The process of claim 1 wherein the consistency of the pulp and the reducing bleaching agent mixture is from above 15% to 50%.
8. In the bleaching of lignocellulosic pulp with a hydrosulfite reducing bleaching agent in an atmosphere substantially free of oxygen at a temperature between about 100 F. and 230 F. wherein the pH of the pulp is maintained at a value between about 4 and 8, the improvement which comprises feeding a semi-solid, nonfiowable, moist mass of pulp in particulate form into an airtight vessel, removing substantially all of the air from said vessel to provide therein an atmosphere substantially free of oxygen, adding to the pulp a solution containing a hydrosulfite selected from the group consisting of zinc, alkali metal and ammonium hydrosulfites and a stabilizer therefor selected from the group consisting of watersoluble polyphosphates, ethylene-diamine-tetra-acetic acid and the alkali metal, alkaline earth metal and ammonium salts thereof, and alkali metal citrates, and mixing mechanically said pulp with said solution in an atmosphere free of oxygen for a period of time sufficient to produce a substantial increase in brightness of said pulp, the respective amounts of the hydrosulfite and of the stabilizer employed being from 0.2% to 5% and from 0.01% to 2% by weight, based on the weight of oven-dry pulp.
9. The process of claim 8 wherein the moist mass of pulp is at a consistency from above 15% to 50%.
10. The process of claim 8 wherein the pulp comprises groundwood.
11. The process of claim 8 wherein the hydrosulfite comprises sodium hydrosulfite.
12. The process of claim 8 wherein the hydrosulfite comprises zinc hydrosulfite.
13. The process of claim 8 wherein the pH of the pulp during bleaching is maintained at a value between about 5 and 7.
14. The process of claim 8 wherein the temperature of tables pulp during bleaching is between about F. and
15. The process of claim 8 wherein the amount of the hydrosulfite employed is from 0.5% to 2% by weight based on the weight of oven-dry pulp.
References Cited in the file of this patent UNITED STATES PATENTS 2,194,956 Taylor Mar. 26, 1940 2,224,159 Parrett Dec. 10, 1940 2,707,144 Sparrow et a1. Apr. 26, 1955 2,707,145 Sparrow et a1 Apr. 26, 1955 OTHER REFERENCES Witham: Modern Pulp and Paper Making, pub. by Reinhold, New York, 1942, p. 283.
Claims (1)
1. THE CONTINUOUS PROCESS OF BLEACHING LIGNOCELLULOSIC PULP WHICH COMPRISES FEEDING INTO AN AIR-TIGHT ZONE A SEMI-SOLID, NON-FLOWABLE, MOIST MASS OF PULP IN PATRICULATE FORM, REMOVING SUBSTANTIALLY ALL OF THE AIR THEREFROM, FORMING A MIXTURE CONTAINING SAID PULP AND A REDUCING BLEACHING AGENT COMPRISING ESSENTIALLY A STABILIZED AQUEOUS SOLUTION OF A HYDROSULFITE SELECTED FROM THE GROUP CONSISTING OF ZINC, ALKALI METAL AND AMMONIUM HYDROSULFITES, THE AMOUNT OF SAID HYDROSULFITE BEING FROM 0.2% TO 5%, BY WEIGHT, OVEN-DRY PULP BASIS, AND MIXING MECHANICALLY SAID PULP WITH SAID HYDROSULFITE IN AN ATMOSPHERE SUBSTANTIALLY FREE OF OXYGEN AT A TEMPERATURE OF FROM 100*F. TO 230*F. FOR A PERIOD OF TIME SUFFICIENT TO PRODUCE A SUBSTANTIALLY INCREASE IN THE PULP BRIGHTNESS, THE PH OF SAID MIXTURE DURING BLEACHING BEING MAINTAINED BETWEEN ABOUT 4 AND 8.
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US724944A US2963395A (en) | 1958-03-31 | 1958-03-31 | Process of bleaching lignocellulosic pulps |
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US724944A US2963395A (en) | 1958-03-31 | 1958-03-31 | Process of bleaching lignocellulosic pulps |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3467574A (en) * | 1966-06-14 | 1969-09-16 | Crown Zellerbach Corp | Refiner bleaching of high yield pulps |
US3467575A (en) * | 1964-08-13 | 1969-09-16 | Hooker Chemical Corp | Process of bleaching paper with peracetic acid |
WO1979000861A1 (en) * | 1978-03-31 | 1979-11-01 | Modo Chemetics Ab | A method of refining cellulose pulps |
EP0155928A1 (en) * | 1984-03-05 | 1985-09-25 | Kamyr, Inc. | Mechanical pulp hydrosulfite bleaching |
EP0639665A1 (en) * | 1993-08-20 | 1995-02-22 | Ciba-Geigy Ag | Phosphate-free reducing and bleaching agent |
DE19704183A1 (en) * | 1997-02-05 | 1998-08-06 | Voith Sulzer Stoffaufbereitung | Bleaching fibres from recycled paper |
US20060142535A1 (en) * | 2004-12-21 | 2006-06-29 | Shane Cyr | Reactive cationic resins for use as dry and wet strength agents in sulfite ion-containing papermaking systems |
US20090205794A1 (en) * | 2005-01-08 | 2009-08-20 | Voith Paper Patent Gmbh | Method for the production of tissue paper |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2194956A (en) * | 1939-01-10 | 1940-03-26 | Mathieson Alkali Works Inc | Bleaching pulp |
US2224159A (en) * | 1937-09-27 | 1940-12-10 | Rayonier Inc | Process for purifying wood pulp |
US2707144A (en) * | 1951-08-08 | 1955-04-26 | Scott Paper Co | Method of bleaching mechanically disintegrated wood pulp |
US2707145A (en) * | 1952-09-11 | 1955-04-26 | Scott Paper Co | Method of bleaching mechanically disintegrated wood pulp |
-
1958
- 1958-03-31 US US724944A patent/US2963395A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2224159A (en) * | 1937-09-27 | 1940-12-10 | Rayonier Inc | Process for purifying wood pulp |
US2194956A (en) * | 1939-01-10 | 1940-03-26 | Mathieson Alkali Works Inc | Bleaching pulp |
US2707144A (en) * | 1951-08-08 | 1955-04-26 | Scott Paper Co | Method of bleaching mechanically disintegrated wood pulp |
US2707145A (en) * | 1952-09-11 | 1955-04-26 | Scott Paper Co | Method of bleaching mechanically disintegrated wood pulp |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3467575A (en) * | 1964-08-13 | 1969-09-16 | Hooker Chemical Corp | Process of bleaching paper with peracetic acid |
US3467574A (en) * | 1966-06-14 | 1969-09-16 | Crown Zellerbach Corp | Refiner bleaching of high yield pulps |
WO1979000861A1 (en) * | 1978-03-31 | 1979-11-01 | Modo Chemetics Ab | A method of refining cellulose pulps |
US4244778A (en) * | 1978-03-31 | 1981-01-13 | Modo-Chemetics Ab | Process for the chemical refining of cellulose pulp |
EP0155928A1 (en) * | 1984-03-05 | 1985-09-25 | Kamyr, Inc. | Mechanical pulp hydrosulfite bleaching |
EP0639665A1 (en) * | 1993-08-20 | 1995-02-22 | Ciba-Geigy Ag | Phosphate-free reducing and bleaching agent |
US5547475A (en) * | 1993-08-20 | 1996-08-20 | Ciba-Geigy Corporation | Phosphate-free reduction bleaching formulation |
DE19704183A1 (en) * | 1997-02-05 | 1998-08-06 | Voith Sulzer Stoffaufbereitung | Bleaching fibres from recycled paper |
US20060142535A1 (en) * | 2004-12-21 | 2006-06-29 | Shane Cyr | Reactive cationic resins for use as dry and wet strength agents in sulfite ion-containing papermaking systems |
US7828934B2 (en) * | 2004-12-21 | 2010-11-09 | Hercules Incorporated | Reactive cationic resins for use as dry and wet strength agents in sulfite ion-containing papermaking systems |
US20090205794A1 (en) * | 2005-01-08 | 2009-08-20 | Voith Paper Patent Gmbh | Method for the production of tissue paper |
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