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US3507743A - Bleaching of wood pulps with reductive bleaching agents and thiourea - Google Patents

Bleaching of wood pulps with reductive bleaching agents and thiourea Download PDF

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Publication number
US3507743A
US3507743A US434627A US3507743DA US3507743A US 3507743 A US3507743 A US 3507743A US 434627 A US434627 A US 434627A US 3507743D A US3507743D A US 3507743DA US 3507743 A US3507743 A US 3507743A
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Prior art keywords
pulp
bleaching
thiourea
weight
pulps
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Expired - Lifetime
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US434627A
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English (en)
Inventor
Louis P Cartsunis
Robert R Kindron
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FMC Corp
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FMC Corp
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    • 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
    • D21C9/1026Other features in bleaching processes
    • D21C9/1036Use of compounds accelerating or improving the efficiency of the processes

Definitions

  • This invention relates to the bleaching of wood pulps containing substantial amounts of non-cellulosic constituents, and particularly to the reductive bleaching of such relatively impure wood pulps by a method which provides bleached pulps resistant to color reversion upon aging.
  • Wood pulps fall generally into two principal classes.
  • One is the so-called purified, or chemical, pulps which are prepared by pulping methods involving chemical removal of much of the non-cellulose wood materials, such as lignins and other impurities, to leave a relatively purified pulp composed of on the order of 80 to 100% of cellulose.
  • These pulping methods involve a chemical digestion, and are typified by the kraft, sulfite and the like methods.
  • the other principal class of wood pulps is prepared by methods which leave the bulk of the non-cellulosic constituents of the wood in the pulp. These methods normally are referred to as mechanical and chemi-mechanical methods, in which the separation of the wood material into fibers operates primarily through mechanical attrition of the wood, either in the form of chips or as logs. Avoidance of strong chemical attack on the wood material leaves the bulk of the non-cellulosic constituents in the fibers. Such fibers contain up to about 60% of cellulose, with the remaining elements in the pulp being on the order of 40 to 60% of non-cellulose wood materials.
  • the strictly mechanical methods for producing pulps are represented by the so-called groundwood process, in which logs or other large pieces of wood are ground on a grinding stone, and the refining methods in which the wood chips are mechanically subdivided in disc or the like refiners.
  • Chemi-mechanical methods involve softening of the wood with aqueous softening agents such as sulfites, bisulfites and the like (without substantial extraction of non-cellulosics) preliminary to mechanical subdivision of the wood into fibers. Pulps produced by either of these essentially mechanical means are referred to herein as low-cellulose wood pulps.
  • the low-cellulose wood pulps are particularly desired because of their low cost and generally satisfactory phys ical properties. Their preparation involves very little loss of the original wood, and methods of producing them are generally less expensive to operate than are the so-called chemical methods. The particular utility of these pulps is in the preparation of printing papers, newsprint, molded products, corrugated paper, boxboards and the like.
  • the reductive bleaching processes are carried out under bleaching conditions at a pH within the range of 2.0 to 8.5 and at a temperature within the range of about to 300 F., and preferably about to 212 F., for up to about 4 hours, and preferably about 0.5 to 1 hour, and normally are carried out in an aqueous pulp slurry containing about 1 to 20%, and preferably about 3%, by weight of the pulp and a bleaching amount of a reductive bleaching agent or mixture of reductive bleaching agents, suitably but not exclusively a hydrosulfite such as sodium or zinc hydrosulfite, thiourea dioxide, or a mixture of an alkali metal borohydride and bisulfite ion.
  • a hydrosulfite such as sodium or zinc hydrosulfite, thiourea dioxide, or a mixture of an alkali metal borohydride and bisulfite ion.
  • the bleaching amount of reductive bleach is normally within the range of 0.01 to 2.0% based on the dry pulp weight, and will be determined for the particular reductive bleach used.
  • a useful thiourea dioxide method is taught in US. Patent No. 3,384,534, issued May 21, 1968, co-pending patent application Ser. No. 418,911, filed Dec. 16, 1964 and assigned to the assignee of this invention, while a useful. borohydride pulp bleaching method is taught in US. Patent No. 3,284,283, issued Nov. 8, 1966, co-pending patent application Ser. No. 345,119 filed Feb. 17, 1964, and also assigned to the assignee of this invention.
  • the thiourea employed in the process of this invention to minimize color reversion in reductive bleaching processes has the following formula:
  • the herein bleaching system either as the solid or dissolved in water or bleaching solution. It can be introduced either prior to or simultaneous with introduction of bleach chemicals.
  • the thiourea is introduced prior to addition of bleaching chemicals.
  • the thiourea is used in the amount of about 0.05 to 1.0% by weight based on the weight of dry pulp. Preferably 0.1 to 0.2% is used.
  • the pulps which are treated by the herein process are the low-cellulose wood pulps, a term which is used herein to define wood pulps containing not more than about 60% by weight of cellulose, with the remaining material being non-cellulose 'wood constituents.
  • These low-cellulose wood pulps are produced from a variety of wood sources, for example, but not exclusively, spruce, fir, hemlock, pine, cottonwood, aspen and poplar.
  • the low-cellulose wood pulps are treated in the present process in the form of an aqueous slurry having a concentration of about 1 to 20% by Weight, and preferably of about 3% by weight.
  • Treatment of slurries containing substantially less than 1% of the pulp is uneconomical, requiring excessive equipment investment, while treatment of pulps having concentrations higher than about 20% is difficult because of the mechanical problems associated with providing good mixing of the treating chemicals with the pulp.
  • the thiourea additive of this invention improves the color reversion properties of bleached pulps prepared with any of the reductive bleaching agents.
  • Typical reductive bleaching agents are sodium or zinc hydrosulfite, thiourea dioxide and a mixture of an alkali metal borohydride with bisulfite ion.
  • the specific conditions employed with the various reducing bleaching agents vary; however, generally speaking they all employ temperatures within the range of about 90 to 300 F., they operate at a pH within the range of about 2.0 to 8.5, and are carried out over a period of up to about 4 hours.
  • the thiourea is employed with them in the amount of about 0.05 to 1.0%, and preferaibly about 0.1 to 0.2%, based on the weight of the pu p.
  • a particularly useful reductive bleaching process employing thiourea dioxide is described fully in co-pending patent applications Ser. No. 418,911, assigned to the assignee of this invention.
  • this process involves treating the low-cellulose wood pulp at about 90 to 300 F., and preferably 90 to 212 F., for up to 4 hours at a pH of about 5.5 to 8.0 in the presence of about 0.1 to 2.0% of thiourea dioxide on the weight of the pulp.
  • the effectiveness of the thiourea dioxide is improved by addition of sodium bisulfite in an amount up to 20 times the amount of weight of thiourea dioxide employed, and/or by addition of polyphosphate, for example sodium tripolyphosphate, in amounts of up to 1% by weight of the Weight of the pulp.
  • the reductive bleaching of pulp may also be carried out with sodium hydrosulfite, by a process in which pulp having a concentration of about 1 to 20% by weight is treated in aqueous slurry form with sodium or zinc hydrosulfite (Na S O or ZnS O employed in the amount of about 0.2 to 1.5% of the Weight of the pulp, at about 90 to 212 F. and a pH in the range of about 4.5 to 8.5 for up to 4 hours.
  • sodium hydrosulfite Na S O or ZnS O employed in the amount of about 0.2 to 1.5% of the Weight of the pulp, at about 90 to 212 F. and a pH in the range of about 4.5 to 8.5 for up to 4 hours.
  • the pH of the aqueous phase of the pulp slurry during the useful reductive bleaching processes ranges from about 2 to 8.5, with the specific range for a given bleaching agent varying within these range limits.
  • the borohydride-bisulfite method is operated at a pH of about 2 to 7, while the thiourea dioxide process preferably is operated at a pH of about 5.5 to 8.0
  • the sodium hydrosulfite process on the other hand is operated at a pH of about 4.5 to 8.5.
  • alkalies such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate or the like are provided in the aqueous phase of the pulp slurry. Amounts of alkali on the order of up to about 0.2% by weight in the solution, or even sometimes as high as 0.4 or 0.5% by weight, are employed to provide the proper pH where required.
  • sodium tripolyphosphate or other polyphosphate and/ or metal chelating agents such as diethylene triamine pentaacetic acid, ethylene diamine tetraacetic acid, and the like, materially improve the bleaching effect of the reductive bleach.
  • Addition of sodium bisulfite also improves the bleach in the thiourea dioxide process, and in the borohydride process it co-acts with the borohydride to provide bleaching.
  • Polyphosphates when employed normally are used in the amount of up to about 1% by weight based on the dry weight of the pulp, and chelating agents are used in amounts up to about 0.5%.
  • Typical useful polyphosphates are sodium tripolyphosphate, tetrasodium pyrophosphate, sodium hexametaphosphate and the like, with potassium polyphosphates being interchangeable with the sodium polyphosphates for all practical purposes.
  • the bleaching process preferably is carried out by slurrying the pulp in water at the desired concentration, and adding the bleaching agents into the pulp slurry. Mild agitation is provided initially to provide even distribution of bleaching chemicals. The temperature is raised to the desired level by external heating means, by passing steam through the pulp slurry, or the like. In small scale operation it is sometimes desirable to carry out the process in an inert non-oxidizing atmosphere, for example by employing a closed vessel with a nitrogen cover. In large scale operation the bulk of the process materials minimizes the oxidative effect of the air with which the system is in contact. Following the bleaching treatment, if desired, although not necessarily, the pulp is washed with water and ether dried or used directly in producing end product.
  • pulp brightnesses were determined on handsheets formed in a B'tichner funnel by TAPPI Test Method T218M-59.
  • the brightnesses of the handsheets were determined on a. Gardner Reflectometer corrected to G.E. Standards, in accordance with TAPPI Test Method T217M-48.
  • the susceptibility of the bleached wet pulps to color reversion was determined by an oxidation treatment involving passing oxygen gas through 3 g. pulp samples.
  • the samples were at a 2.0% oven dry pulp concentration, and 750 ml. of oxygen gas was passed through the samples in 3 minutes while the pulp temperature was held at F.
  • the brightness reversions, otherwise expressed as drops in GE. brightness values, produced by this test correlate closely with the behavior of pulps bleached by the procedures of the examples when such pulps are handled by customary transfer, mixing and other procedures over the usual times, e.g. 4 to 20 hours, in pulp from during manufacture of articles from the pulp.
  • EXAMPLE 1 Two samples of a West Coast pine refiner groundwood, having an unbleached G.E. brightness of 50.3% were slurn'ed with boiling dilution water in a slow speed paddle mixer to a concentration slightly higher than 3% by Weight on an oven-dry pulp basis, such that subsequent addition of bleaching and other treating chemicals provided a final pulp concentration of 3% by weight. Five tenths percent by weight based on the weight of the pulps of sodium tripolyphosphate was then mixed into each of the slurries in a Waring blender, and the resulting pulps were transferred into polypropylene bottles, and purged of air with compressed nitrogen gas.
  • Example 2 The procedure of Example 1 was followed with the exception that the Example 1 reductive bleaching system of sodium hydrosulfite and sodium tripolyphosphate was replaced with 0.75% by weight of thiourea dioxide, 0.2% of sodium hydroxide, and 0.5% of sodium tripolyphosphate, all based on the weight of the pulp. One-tenth percent by weight of the thiourea on the weight of the pulp was employed in one sample and no thiourea was used in the other. The pH of the slurries during bleaching was about 6.0.
  • the brightness of the pulp sample bleached in the presence of thiourea as an additive in accordance with this invention was 60.7%, whereas the brightness of the corresponding pulp bleached without the thiourea was 58.8%; both pulps were tested after the above-described oxidation treatment of the bleached pulp.
  • Example 3 The procedure of Example 1 was followed with the exception that the sodium hydrosulfide-sodium tripolyphosphate bleaching system of Example 1 was replaced with 0.05% by weight of sodium borohydride, 3.1% by weight of sodium bisulfite, and 0.5% by weight of sodium tripolyphosphate, all based on the weight of the pulp.
  • Onetenth percent by weight of thiourea on the weight of the pulp was employed in one sample and no thiourea was used in the other.
  • the pH of the slurries during bleaching was. about 6.0.
  • the pulp bleached with the system containing the thiourea additive of this invention was 63.2% following the oxidation treatment described above, whereas the brightness of the pulp bleached without the thiourea was only 60.4% following the oxidation treatment.
  • Example 4 The procedure of Example 1 was followed with the exception that the pulp treated was a northern fir-balsam stone groundwood pulp having an initial brightness of 60.2%, and the sodium hydrosulfite-sodium tripolyphosphate bleaching system employed in Example 1 was replaced with sodium borohydride in the amount of 0.1%, sodium bisulfite in the amount of 1.1%, and sodium tripolyphosphate in the amount 0.5% all based on the weight of the pulp.
  • One-tenth percent of thiourea was employed in one sample and no thiourea was used in the other.
  • the pH of the slurries during bleaching was about 5.5 to 6.0.
  • the brightness of the pulp following oxidation by the above procedure was 71.4%.
  • the bleach not involving the use of thiourea produced a pulp which following oxidation had a brightness of only 69.5%.
  • Example 5 The procedure of Example 1 was followed with the exceptions that the pulp treated was northern pine stone groundwood having an initial brightness of 55.9%, and that in place of the sodium hydrosulfite-sodium tripolyphosphate bleaching system, 0.5 of thioureau dioxide, 3.3% of sodium bisulfite, 0.5 of sodium hydroxide and 0.5% of sodium tripolyphosphate, all based on the weight of the pulp, were employed as the bleaching system. Thiourea was employed in the amount of 0.1% based on the weight of the pulp with one sample, and no thiourea was used in the other. The pH of the pulp slurries during bleaching was about 7.0, and they were maintained at 160 F. for three hours rather than 4 hours as in Example 1.
  • the brightness of the pulp bleached with the system containing the thiourea additive of this invention had a brightness of 65.6% following the oxidation treatment described above, whereas the pulp bleached with the system not containing thiourea had a brightness of only 63.8% after the oxidation treatment.
  • EXAMPLE 7 Eifect of thiourea concentration
  • the procedure of Example 1 was followed to bleach a series of pulp samples in the presence of varying amounts of thiourea.
  • the pulp bleached was West Coast fir refiner groundwood having an unbleached brightness of 52.6%, and the bleaching chemicals were sodium hydrosulfite in the amount of 1.25%, and sodium tripolyphosphate in the amount of 0.5%, by weight based on the weight of the pulp.
  • a series of samples was made, the first containing no thiourea, and five others containing thiourea in the amounts shown in Table 1 which follows.
  • the thiourea was added to the pulp prior to introduction of the sodium hydrosulfite and sodium tripolyphosphate.
  • the pH of the slurries during bleaching was about 5.7 to 6.0, and the pulps were mtaintained at F. for 3.5 hours.
  • the results of the series of bleaches are shown in Table 1 which follows:
  • the improvement in brightness retention represents a real advantage in the bleaching of low-cellulose wood pulps, making it possible to use the pulps directly in applications in which such pulps could not heretofore be employed.

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
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US434627A 1965-02-23 1965-02-23 Bleaching of wood pulps with reductive bleaching agents and thiourea Expired - Lifetime US3507743A (en)

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US (1) US3507743A (xx)
BE (1) BE676663A (xx)
DE (1) DE1546253A1 (xx)
DK (1) DK109015C (xx)
ES (1) ES322925A1 (xx)
FI (1) FI43809B (xx)
GB (1) GB1095280A (xx)
NL (1) NL6601601A (xx)
SE (1) SE314580B (xx)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4002526A (en) * 1975-10-10 1977-01-11 International Paper Company Oxygen-alkali delignification of low consistency wood pulp
US4244780A (en) * 1979-11-15 1981-01-13 Nalco Chemical Company Use of thiourea dioxide in pulp bleaching processes to preserve pulp strength and aid in brightness
US4675076A (en) * 1986-10-01 1987-06-23 Ppg Industries, Inc. Method for brightening pulp
US5338402A (en) * 1987-05-25 1994-08-16 Societe Atochem Process for preparing a bleached chemithermomechanical pulp
US5958184A (en) * 1992-06-10 1999-09-28 Mitsubishi Gas Chemical Company Inc. Process for producing thiourea dioxide
EP1132517A1 (en) * 2000-03-06 2001-09-12 Georgia-Pacific Corporation Method of providing bleached papermaking fibres with durable curl and their absorbent products
US20010020521A1 (en) * 1995-10-20 2001-09-13 Andritz-Ahlstrom Inc. Acid treatment of pulp at high temperature in connection with bleaching
US6428653B1 (en) 2000-12-04 2002-08-06 West Fraser Timber Co. Ltd. Method of bleaching with formamidine sulfinic acid using a reducing agent to eliminate residual peroxide
US20050145348A1 (en) * 2000-03-06 2005-07-07 Lee Jeffrey A. Method of providing paper-making fibers with durable curl and absorbent products incorporating same
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
WO2025016539A1 (en) * 2023-07-18 2025-01-23 Basf Se Process for producing mechanical wood pulp

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2071304A (en) * 1934-12-04 1937-02-16 Great Western Electro Chemical Co Process of manufacture of products of ground wood pulp

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2071304A (en) * 1934-12-04 1937-02-16 Great Western Electro Chemical Co Process of manufacture of products of ground wood pulp

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4002526A (en) * 1975-10-10 1977-01-11 International Paper Company Oxygen-alkali delignification of low consistency wood pulp
US4244780A (en) * 1979-11-15 1981-01-13 Nalco Chemical Company Use of thiourea dioxide in pulp bleaching processes to preserve pulp strength and aid in brightness
US4675076A (en) * 1986-10-01 1987-06-23 Ppg Industries, Inc. Method for brightening pulp
US5338402A (en) * 1987-05-25 1994-08-16 Societe Atochem Process for preparing a bleached chemithermomechanical pulp
US5958184A (en) * 1992-06-10 1999-09-28 Mitsubishi Gas Chemical Company Inc. Process for producing thiourea dioxide
US20010020521A1 (en) * 1995-10-20 2001-09-13 Andritz-Ahlstrom Inc. Acid treatment of pulp at high temperature in connection with bleaching
US6306253B2 (en) 1995-10-20 2001-10-23 Andritz-Ahlstrom Oy Acid treatment of pulp at high temperature prior to chlorine dioxide bleaching
US7291247B2 (en) 2000-03-06 2007-11-06 Georgia-Pacific Consumer Operations Llc Absorbent sheet made with papermaking fibers with durable curl
EP1132517A1 (en) * 2000-03-06 2001-09-12 Georgia-Pacific Corporation Method of providing bleached papermaking fibres with durable curl and their absorbent products
US6627041B2 (en) 2000-03-06 2003-09-30 Georgia-Pacific Corporation Method of bleaching and providing papermaking fibers with durable curl
US20040016524A1 (en) * 2000-03-06 2004-01-29 Lee Jeffrey A. Method of bleaching and providing papermaking fibers with durable curl
US20050145348A1 (en) * 2000-03-06 2005-07-07 Lee Jeffrey A. Method of providing paper-making fibers with durable curl and absorbent products incorporating same
US8277606B2 (en) 2000-03-06 2012-10-02 Georgia-Pacific Consumer Products Lp Method of providing paper-making fibers with durable curl and absorbent products incorporating same
US6428653B1 (en) 2000-12-04 2002-08-06 West Fraser Timber Co. Ltd. Method of bleaching with formamidine sulfinic acid using a reducing agent to eliminate residual peroxide
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
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
KR101270913B1 (ko) * 2004-12-21 2013-06-03 허큘레스 인코포레이티드 아황산 이온-함유 제지 계에서 건조 및 습윤 강화제로사용하기 위한 반응성 양이온성 수지
CN101120138B (zh) * 2004-12-21 2013-06-05 赫尔克里士公司 在含有亚硫酸盐离子的造纸体系中用作干和湿强度剂的活性阳离子树脂
WO2025016539A1 (en) * 2023-07-18 2025-01-23 Basf Se Process for producing mechanical wood pulp

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ES322925A1 (es) 1966-11-16
FI43809B (xx) 1971-03-01
DK109015C (da) 1968-03-04
GB1095280A (en) 1967-12-13
SE314580B (xx) 1969-09-08
NL6601601A (xx) 1966-08-24
BE676663A (xx) 1966-07-18
DE1546253A1 (de) 1970-04-30

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