US2938826A - Bleaching of cellulosic pulp - Google Patents

Bleaching of cellulosic pulp Download PDF

Info

Publication number
US2938826A
US2938826A US758557A US75855758A US2938826A US 2938826 A US2938826 A US 2938826A US 758557 A US758557 A US 758557A US 75855758 A US75855758 A US 75855758A US 2938826 A US2938826 A US 2938826A
Authority
US
United States
Prior art keywords
pulp
bleaching
chlorate
suspension
chlorates
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
Application number
US758557A
Inventor
Marpillero Paolo
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AMELIORATION ET LE DEV DES PRO
POUR L'AMELIORATION ET LE DEVELOPMENT DES PROCEDES INDUSTRIELS Ste
Original Assignee
AMELIORATION ET LE DEV DES PRO
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by AMELIORATION ET LE DEV DES PRO filed Critical AMELIORATION ET LE DEV DES PRO
Application granted granted Critical
Publication of US2938826A publication Critical patent/US2938826A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00After-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
    • D21C9/10Bleaching ; Apparatus therefor
    • D21C9/12Bleaching ; Apparatus therefor with halogens or halogen-containing compounds
    • D21C9/14Bleaching ; Apparatus therefor with halogens or halogen-containing compounds with ClO2 or chlorites

Definitions

  • the present application is a continuation-in-partof my application Serial No. 520,089, filed 'July 5, 1955, now abandoned.
  • the present invention has for its object a process of lignin removal from and bleaching of cellulosic fibers. It is characterized in that the fibers in a slightly acidulated aqueous suspension are treated with metallic chlorates in the presence of a catalyst.
  • the present invention is differentiated from these prior this quantity is several times, indeed tens of times, larger than said quantity.
  • the quantity of the acid used in the present invention can be 200300 times smaller than that used in the processes alluded to.
  • the temperatures and reaction times can, on the contrary, remain of comparable magnitude.
  • chlorates in acid concentrations not higher than 0.2% and at temperatures not higher than 80 C. is made possible, according to the present invention, by the use of certain catalysts.
  • the quantity of chlorates used in the present invention ranges from 0.2% to based on the weight of the material treated. Since the material treated is always in the form of an aqueous suspension, it is important to reduce the quantity of water to the minimum possible.
  • suspensions are used having a density of at least 10% (i.e. 10 litres of Water contain 1 kilo of dry fibers) which corresponds to the densities ordinarily used in bleaching pulp.
  • higher densities can be used, for example, a density of 50%.
  • the quantities of acid to be used are in all instances l-2 grams per litre of liquid present during the treat- 2,938,826- Patented May 31, 1960 ment (namely, 01-02%).
  • acids there can be used H HCl, or any other acid capable of yielding a pH lower than 3.
  • the temperatures to be used are lower than 80 C., for example, a temperature of 60-70 C., at which the consumption (exhaustion) of the chlorate requires 4-8 hours, or a temperature of 20 C. which requires a treatment period of 3-4 days.
  • the oxidizing action exerted by the chlorate on the cellulosic fibers can be considered as being difierent from that exerted by the C10 by the simple fact that the C10 utilizes two atoms of oxygen for oxidizing the fibers whereas, when chlorates are used-for example, NaClO three atoms of oxygen participate in the oxidation of the fibers, NaCl being the only residue of the operation.
  • this quantity of chlorate depends on the quantity of lignin contained in the material being treated and on the desired subsequent treatments. Indeed, the operation, the ultimate aim of which is bleaching, is completed by a treatment subsequent to that with the chlorate, for example, with hypochlorites or peroxides. The bleaching can also be initiated with the usual treatments and be completed by means 'of chlorates in accordance with the present invention. The use of a larger quantity of chlorates renders possible a reduction in the quantity of reagents used in the subsequent treatments, and vice versa.
  • a catalyst containing vanadium there is used a catalyst containing vanadium.
  • a catalyst having a base of vanadium and tin gives excellent results. The operation proceeds as if the reaction takes place directly between the chlorate and lignified constituents contained in the cellulosic fibers, the residue of the operation being NaCl.
  • the process according to the invention makes it pos sible to obtain for the same degree of whiteness a greater yield in weight of bleached pulp and viscosities higher than there can be obtained with other bleaching processes which do not use chlorates.
  • Example 1 gr. of straw, suitably cut into pieces about 3-4 cm. long, are suspended in 500 gr. water containing 6 gr. sodium chlorate, to which is added 1 gr. H 801 and a catalyst consisting of a mixture of vanadium and tin salts, for example, 0.06 gr. V 0 and 0.025 gr. SnCl
  • the suspension is maintained at a temperature of 70 C. with stirring, until the chlorate has been exhausted, which can be effected in 6 to 8 hours at a temperature of 70 C.; the resultant product is extracted with NaOH and washed, and can be separated into fibers by the use of known apparatus.
  • the resultant pulp has a bleaching index (TAPPI T 2l9-M48) of 68 and can be bleached later by known means.
  • Example 2 100 gr. of semi-chemical coniferous cellulose, having a bleaching index of 12.5 were suspended in 1 litre cold water. 1 gr. HCl, 5 gr. NaClO and 0.02 gr. NH VO +0.0l gr. SnO; were added while agitating continuously. The suspension was gently heated and maintained at 65 C. temperature for 6 hours, agitating all the while. Thereafter, the cellulose was washed with water at 40 C., slightly alkalinized with NaOH, yieldcan be bleached further by known means.
  • This pulp Example I 100 gr. kraft cellulose, having a bleaching index of 12.5 were treated in exactly the same way as in Example 2, yielding a pulp with a bleaching index of 1.50.
  • Example 4 100 gr. sulfite cellulose derived from leaiy'rwood and having a bleaching index of 7.00 were treated exactly in the same way as in Example 2, but using 25 gr. NaClO 0.01 gr. N H VO 0.005 gr. SnO and 0.5 gr. HCl. The resulting pulp has a bleaching index'of 0.5.
  • Example 6 100 gr. sulfite cellulose having a bleaching index of 8 were treated as in Example 2 with 2.2 gr. NaClO 0.70 gr. H 80 and 0.09 gr. NH VO A pulp was obtained having a bleaching index of 1.00.
  • Example 7 100 gr. of sulfite cellulose were bleached by a known process, withoutthe use of chlorites or of C10 so as to attain a whiteness (brightness) of 76 GE while retaining a satisfactory viscosity.
  • the pulp was dispersed in 1 litre of water and there were added: 1 gr. Na'ClO 0.01 gr. V 0 and 0.5 gr. H 80 The pulp was heated to 70 C. and kept at this temperature for 6 hours with light stirring. A pulp was obtained having a whiteness .(brightness) of 87 GE and viscosity equal to about 90% of the initial viscosity.
  • Example 8 100 gr. of the same pulp as in Example 7, but dispersed in only 100 gr. water, are treated with an aqueous solution of the same chemicals as in said example, the dispersion being permitted to stand for a period of 3-4 .days at the ambient temperature. There is obtained a whiteness (brightness) of 87 GE and a pulp having a viscosity in excess of 90% of that of the original pulp. It is apparent that the consistency (density) of the pulp suspension does not affect the results of the treatment.
  • Example 9 2,988,895.
  • I 7 a V7 Instead of using a solution of chlorine in water, gaseous chlorine can be injected into the aqueous suspenslon.
  • treating conditions of the process according to the invention depend on the nature 'of the cellulosic material submitted to treatment, as well as on the treatments to'which the starting material has been subjected.
  • All the reagents employed in the application of the present invention can be added separately, and at the time of use, to the aqueous suspension of cellulosic fibers to be treated. Nevertheless, the-chlorate and the catalysts can be mixed preliminarily.
  • chlorates'of other'alkali and alkaline earth metals can also be employed in the performance of the present invention.
  • Particularly useful in this connection are the chlorates of potassium, calcium and barium.
  • chemical cellulosefas used in the specification and in the appended claims denotes substantially delignified cellulose fibers which have been isolated from wood chips or any kind of vegetable raw material by chemical digestion.
  • semi-chemical cellulose denotes fibers derived from any kind of vegetable raw material and which are partially delignified and thereafter separated by chemical means.
  • the present invention has been especially devised to enable'effective and economic treatment of such chemical and semi-chemical cellulose, also straw, i.e. materials characterized by a low lignin content.
  • a process for bleaching chemical or semi-chemical cellulose pulps comprising the step of contacting an aqueous suspension of the pulp, at a temperature within the range of 2080 C., with a metallic chlorate selected from the group consisting of the alkali metal chlorates and alkaline earth metal chlorates, in the presence of a vanadium catalyst, said chlorate being present in an amount within the range of 02-10% by weight of the pulp, and said suspension containing 1-2 grams acid per litre of suspension.

Description

United States Patent BLEACHING OF CELLULOSIC PULP Paolo Marpillero, Milan, Italy, assignor to Societe pour lAmelioration et le Development des Procedes Industriels (SADEPI), a corporation of Tangier No Drawing. Filed Sept. 2, 1958, Ser. No. 758,557
Claims priority, application France July 24, 1954 3 Claims. (Cl. 162-87) The present application is a continuation-in-partof my application Serial No. 520,089, filed 'July 5, 1955, now abandoned. The present invention has for its object a process of lignin removal from and bleaching of cellulosic fibers. It is characterized in that the fibers in a slightly acidulated aqueous suspension are treated with metallic chlorates in the presence of a catalyst.
It has already been proposed to treat cellulosic fibers in the form of wood chips with large quantities of chlorates in an acid medium in order to obtain a raw pulp.
The present invention is differentiated from these prior this quantity is several times, indeed tens of times, larger than said quantity.
Further, the quantity of the acid used in the present invention can be 200300 times smaller than that used in the processes alluded to. The temperatures and reaction times can, on the contrary, remain of comparable magnitude.
This enormous difference in the means used in the present invention not only has an economic advantage, which is self-evident, but makes it also possible to limit the attack on the cellulosic fibers, which is inevitable in any acidic medium. This attack is the more intensive the more concentrated the medium. It becomes even more intensive as the fibers, as the result of the bleaching, attain (approach) a progressively higher degree of purity.
It is known that a cellulosic fiber having a degree of purity approaching that of the complete bleached state, is very much degraded if exposed for a few hours to the action of an acidic medium having a H 80 concentration higher than 0.5%, for example, 1% at a temperature higher than the ambient temperature but lower than 80 C., for example, 4070 C.
The use of chlorates in acid concentrations not higher than 0.2% and at temperatures not higher than 80 C. is made possible, according to the present invention, by the use of certain catalysts.
The quantity of chlorates used in the present invention ranges from 0.2% to based on the weight of the material treated. Since the material treated is always in the form of an aqueous suspension, it is important to reduce the quantity of water to the minimum possible. Preferably, suspensions are used having a density of at least 10% (i.e. 10 litres of Water contain 1 kilo of dry fibers) which corresponds to the densities ordinarily used in bleaching pulp. However, higher densities can be used, for example, a density of 50%.
The quantities of acid to be used are in all instances l-2 grams per litre of liquid present during the treat- 2,938,826- Patented May 31, 1960 ment (namely, 01-02%). As acids, there can be used H HCl, or any other acid capable of yielding a pH lower than 3.
The temperatures to be used are lower than 80 C., for example, a temperature of 60-70 C., at which the consumption (exhaustion) of the chlorate requires 4-8 hours, or a temperature of 20 C. which requires a treatment period of 3-4 days.
While it is possible that under these conditions formation of C10 takes place (which, however, cannot be established by known analytical means), the oxidizing action exerted by the chlorate on the cellulosic fibers can be considered as being difierent from that exerted by the C10 by the simple fact that the C10 utilizes two atoms of oxygen for oxidizing the fibers whereas, when chlorates are used-for example, NaClO three atoms of oxygen participate in the oxidation of the fibers, NaCl being the only residue of the operation.
In carrying out the present invention, there is added to the suspension of cellulosic fibers the requisite quantity of chlorate--for example, NaClO which it is desired shall be consumed (absorbed) by the material being treated.
Applicants experience has shown that this quantity of chlorate depends on the quantity of lignin contained in the material being treated and on the desired subsequent treatments. Indeed, the operation, the ultimate aim of which is bleaching, is completed by a treatment subsequent to that with the chlorate, for example, with hypochlorites or peroxides. The bleaching can also be initiated with the usual treatments and be completed by means 'of chlorates in accordance with the present invention. The use of a larger quantity of chlorates renders possible a reduction in the quantity of reagents used in the subsequent treatments, and vice versa.
According to a preferred form of the invention, there is used a catalyst containing vanadium. A catalyst having a base of vanadium and tin gives excellent results. The operation proceeds as if the reaction takes place directly between the chlorate and lignified constituents contained in the cellulosic fibers, the residue of the operation being NaCl.
The process according to the invention makes it pos sible to obtain for the same degree of whiteness a greater yield in weight of bleached pulp and viscosities higher than there can be obtained with other bleaching processes which do not use chlorates.
The examples set out below, which are not given by way of limitation, but only by way of illustration, describe various embodiments of the present invention:
Example 1 gr. of straw, suitably cut into pieces about 3-4 cm. long, are suspended in 500 gr. water containing 6 gr. sodium chlorate, to which is added 1 gr. H 801 and a catalyst consisting of a mixture of vanadium and tin salts, for example, 0.06 gr. V 0 and 0.025 gr. SnCl The suspension is maintained at a temperature of 70 C. with stirring, until the chlorate has been exhausted, which can be effected in 6 to 8 hours at a temperature of 70 C.; the resultant product is extracted with NaOH and washed, and can be separated into fibers by the use of known apparatus. The resultant pulp has a bleaching index (TAPPI T 2l9-M48) of 68 and can be bleached later by known means.
Example 2 100 gr. of semi-chemical coniferous cellulose, having a bleaching index of 12.5 were suspended in 1 litre cold water. 1 gr. HCl, 5 gr. NaClO and 0.02 gr. NH VO +0.0l gr. SnO; were added while agitating continuously. The suspension was gently heated and maintained at 65 C. temperature for 6 hours, agitating all the while. Thereafter, the cellulose was washed with water at 40 C., slightly alkalinized with NaOH, yieldcan be bleached further by known means.
ring a pulp with a bleaching index or 1.00. This pulp Example I 100 gr. kraft cellulose, having a bleaching index of 12.5 were treated in exactly the same way as in Example 2, yielding a pulp with a bleaching index of 1.50.
Example 4 100 gr. sulfite cellulose derived from leaiy'rwood and having a bleaching index of 7.00 were treated exactly in the same way as in Example 2, but using 25 gr. NaClO 0.01 gr. N H VO 0.005 gr. SnO and 0.5 gr. HCl. The resulting pulp has a bleaching index'of 0.5.
Example 100 gr. sulfite' cellulose, derived from coniferous plants and having a bleaching index of 8, were treated as in Example 2 with 2.2 gr. NaClO 0.45 gr. HCl, 0.009 gr. NH VO and 0.0045 SnO There was obtained a pulp having a bleaching index of 1.
I Example 6 100 gr. sulfite cellulose having a bleaching index of 8 were treated as in Example 2 with 2.2 gr. NaClO 0.70 gr. H 80 and 0.09 gr. NH VO A pulp was obtained having a bleaching index of 1.00.
Example 7 100 gr. of sulfite cellulose were bleached by a known process, withoutthe use of chlorites or of C10 so as to attain a whiteness (brightness) of 76 GE while retaining a satisfactory viscosity. The pulp was dispersed in 1 litre of water and there were added: 1 gr. Na'ClO 0.01 gr. V 0 and 0.5 gr. H 80 The pulp was heated to 70 C. and kept at this temperature for 6 hours with light stirring. A pulp was obtained having a whiteness .(brightness) of 87 GE and viscosity equal to about 90% of the initial viscosity.
Example 8 100 gr. of the same pulp as in Example 7, but dispersed in only 100 gr. water, are treated with an aqueous solution of the same chemicals as in said example, the dispersion being permitted to stand for a period of 3-4 .days at the ambient temperature. There is obtained a whiteness (brightness) of 87 GE and a pulp having a viscosity in excess of 90% of that of the original pulp. It is apparent that the consistency (density) of the pulp suspension does not affect the results of the treatment.
Example 9 2,988,895. I 7 a V7 Instead of using a solution of chlorine in water, gaseous chlorine can be injected into the aqueous suspenslon.
Various treatments can be applied to these same cellulosic fibers by interposing iptermediate washings or other treatments.
It is evident that the actual (practical). treating conditions of the process according to the invention depend on the nature 'of the cellulosic material submitted to treatment, as well as on the treatments to'which the starting material has been subjected.
All the reagents employed in the application of the present invention can be added separately, and at the time of use, to the aqueous suspension of cellulosic fibers to be treated. Nevertheless, the-chlorate and the catalysts can be mixed preliminarily.
While sodium chlorate has been used in the examples set out above, the chlorates'of other'alkali and alkaline earth metals can also be employed in the performance of the present invention. Particularly useful in this connection are the chlorates of potassium, calcium and barium.
The term chemical cellulosefas used in the specification and in the appended claims denotes substantially delignified cellulose fibers which have been isolated from wood chips or any kind of vegetable raw material by chemical digestion. Similarly, the term semi-chemical cellulose denotes fibers derived from any kind of vegetable raw material and which are partially delignified and thereafter separated by chemical means. As has beenindicated above, the present invention has been especially devised to enable'effective and economic treatment of such chemical and semi-chemical cellulose, also straw, i.e. materials characterized by a low lignin content.
I claim:
1. In a process for bleaching chemical or semi-chemical cellulose pulps, the improvement which comprises the step of contacting an aqueous suspension of the pulp, at a temperature within the range of 2080 C., with a metallic chlorate selected from the group consisting of the alkali metal chlorates and alkaline earth metal chlorates, in the presence of a vanadium catalyst, said chlorate being present in an amount within the range of 02-10% by weight of the pulp, and said suspension containing 1-2 grams acid per litre of suspension. i
2. A process according to claim 1, wherein sodium chlorate is used.
3. Process according to claim 1, characterized in that the catalyst comprises vanadium and tin.
References Cited the file of this patent UNlTED STATES PATENTS OTHER REFERENCES Casciana Paper Trade Journal, Sept. 5, 1952, pages 22, 24, 26, 28, 30, 32. V
Casciani Paper Trade Journal, Mar. 6,' 1953, pages

Claims (1)

1. IN A PROCESS FOR BLEACHING CHEMICAL OR SEMI-CHEMICAL CELLULOSE PULPS, THE IMPROVEMENT WHICH COMPRISES THE STEP OF CONTACTING AN AQUEOUS SUSPENSION OF THE PULP, AT A TEMPERATURE WITHIN THE RANGE OF 20*-80*C., WITH A METALLIC CHLORATE SELECTED FROM THE GROUP CONSISTING OF THE ALKALI METAL CHLORATES AND ALKALINE EARTH METAL CHLORATES, IN THE PRESENCE OF A VANDIUM CATALYST, SAID CHLORATE BEING PRESENT IN AN AMOUNT WITHIN THE RANGE OF 0.2-10% BY WEIGHT OF THE PULP, AND SAID SUSPENSION CONTAINING 1-2 GRAMS ACID PER LITRE OF SUSPENSION.
US758557A 1954-07-24 1958-09-02 Bleaching of cellulosic pulp Expired - Lifetime US2938826A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR2938826X 1954-07-24

Publications (1)

Publication Number Publication Date
US2938826A true US2938826A (en) 1960-05-31

Family

ID=9690138

Family Applications (1)

Application Number Title Priority Date Filing Date
US758557A Expired - Lifetime US2938826A (en) 1954-07-24 1958-09-02 Bleaching of cellulosic pulp

Country Status (1)

Country Link
US (1) US2938826A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3138947A (en) * 1958-10-18 1964-06-30 Kamyr Ab Device for continuous bleaching of cellulose
US3259659A (en) * 1960-06-22 1966-07-05 Studiengesellschaft Kohle Mbh Process for the production of boron alkyls containing methyl groups
US4039374A (en) * 1975-08-29 1977-08-02 Union Camp Corporation Bleaching of cellulosic pulp fibers with chlorine dioxide in the presence of a vanadium compound
US4702807A (en) * 1986-10-02 1987-10-27 International Paper Company Electrochemical process for bleaching wood pulp using chlorate and a redox catalyst
US5330620A (en) * 1992-02-25 1994-07-19 Pulp And Paper Research Institute Of Canada Bleaching pulp with chloric acid
CN104098704A (en) * 2013-04-15 2014-10-15 金东纸业(江苏)股份有限公司 Preparation method for paper pulp containing multiple functional groups

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US321452A (en) * 1885-07-07 Goldsbtjby haedbn pond
US1777751A (en) * 1926-08-05 1930-10-07 Ig Farbenindustrie Ag Producing cellulose
US1904190A (en) * 1929-08-26 1933-04-18 Becher Willy Process of manufacturing chlorine dioxide
US2477631A (en) * 1945-02-21 1949-08-02 Ecusta Paper Corp Catalytic bleaching with chlorites
US2480148A (en) * 1948-10-14 1949-08-30 Ecusta Paper Corp Catalytic bleaching process

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US321452A (en) * 1885-07-07 Goldsbtjby haedbn pond
US1777751A (en) * 1926-08-05 1930-10-07 Ig Farbenindustrie Ag Producing cellulose
US1904190A (en) * 1929-08-26 1933-04-18 Becher Willy Process of manufacturing chlorine dioxide
US2477631A (en) * 1945-02-21 1949-08-02 Ecusta Paper Corp Catalytic bleaching with chlorites
US2480148A (en) * 1948-10-14 1949-08-30 Ecusta Paper Corp Catalytic bleaching process

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3138947A (en) * 1958-10-18 1964-06-30 Kamyr Ab Device for continuous bleaching of cellulose
US3259659A (en) * 1960-06-22 1966-07-05 Studiengesellschaft Kohle Mbh Process for the production of boron alkyls containing methyl groups
US4039374A (en) * 1975-08-29 1977-08-02 Union Camp Corporation Bleaching of cellulosic pulp fibers with chlorine dioxide in the presence of a vanadium compound
US4702807A (en) * 1986-10-02 1987-10-27 International Paper Company Electrochemical process for bleaching wood pulp using chlorate and a redox catalyst
US5330620A (en) * 1992-02-25 1994-07-19 Pulp And Paper Research Institute Of Canada Bleaching pulp with chloric acid
CN104098704A (en) * 2013-04-15 2014-10-15 金东纸业(江苏)股份有限公司 Preparation method for paper pulp containing multiple functional groups
US20140305603A1 (en) * 2013-04-15 2014-10-16 Goldeast Paper (Jiangsu) Co., Ltd Process for making pulp

Similar Documents

Publication Publication Date Title
US4661205A (en) Method of bleaching lignocellulosic material with peroxide catalyzed with a salt of a metal
US4372812A (en) Chlorine free process for bleaching lignocellulosic pulp
US4451332A (en) Method for delignification of ligno-cellulose containing fiber material with an alkali-oxygen extraction stage
US2466633A (en) Method of bleaching cellulosic pulp
CA1129161A (en) Delignification and bleaching process and solution for lignocellulosic pulp with peroxide in the presence of metal additives
US4938842A (en) High consistency peroxide bleaching
US2938826A (en) Bleaching of cellulosic pulp
US3366534A (en) Complete chemical system for a kraft mill
US3100732A (en) Process of bleaching wood pulp by combined treatment with peroxide and an alkali metal borohydride
US4560437A (en) Process for delignification of chemical wood pulp using sodium sulphite or bisulphite prior to oxygen-alkali treatment
US3284283A (en) Production of wood pulps including treatment of cellulosic fibers with bisulfite ion followed by alkali metal borohydride
EP0464110B1 (en) Bleaching process for the production of high bright pulps
US3384534A (en) Bleaching of wood pulps with thiourea dioxide
US3177111A (en) Hypochlorite sulfamic acid process of bleaching cellulosic materials
US2962413A (en) Method of producing cellulosic pulp
US2249646A (en) Bleaching cellulose with titanium compounds
US2527563A (en) Method of bleaching semichemical pulps
US2195302A (en) Bleaching pulp
NO143752B (en) PROCEDURE FOR BLAKING AND REMOVING LIGNIN FROM TREMASS
US1774403A (en) Process of producing fiber of high alpha cellulose content
US1953191A (en) Process of refining cellulose
US3619349A (en) Bleaching of shredded or fluffed cellulosic pulp with gaseous chlorine monoxide
US2235837A (en) Bleaching cellulose
US2947657A (en) Extraction of cellulose from vegetable matter
US1768819A (en) Bleaching