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WO1988004706A1 - Method for washing of alcaline pulp - Google Patents

Method for washing of alcaline pulp Download PDF

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Publication number
WO1988004706A1
WO1988004706A1 PCT/SE1987/000623 SE8700623W WO8804706A1 WO 1988004706 A1 WO1988004706 A1 WO 1988004706A1 SE 8700623 W SE8700623 W SE 8700623W WO 8804706 A1 WO8804706 A1 WO 8804706A1
Authority
WO
WIPO (PCT)
Prior art keywords
washing
pulp
carbon dioxide
stage
filtrate
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.)
Ceased
Application number
PCT/SE1987/000623
Other languages
French (fr)
Inventor
Monica BOKSTRÖM
Raimo Rasimus
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.)
Linde Sverige AB
Original Assignee
AGA AB
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
Priority claimed from SE8605510A external-priority patent/SE8605510L/en
Application filed by AGA AB filed Critical AGA AB
Priority to BR8707606A priority Critical patent/BR8707606A/en
Priority to JP63501165A priority patent/JPH0778315B2/en
Priority to AT88900488T priority patent/ATE67536T1/en
Publication of WO1988004706A1 publication Critical patent/WO1988004706A1/en
Priority to NO883736A priority patent/NO172550C/en
Priority to FI883851A priority patent/FI90256C/en
Anticipated expiration legal-status Critical
Ceased 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
    • D21C9/02Washing ; Displacing cooking or pulp-treating liquors contained in the pulp by fluids, e.g. wash water or other pulp-treating agents

Definitions

  • a further object of the present invention is to emascu ⁇ late alkaline, cellulosic pulp of sodium ions.
  • a third obj ect of the present invention is to increase the washing-out , from alkaline, cell ulosic pulp, of substances which contribute to chemical oxygen demand (COD) .
  • the washed pulp departs from the fourth filter 18 at reference numeral 13.
  • the filter cake is comminuted by shredders 8.
  • Filtrate from one filter is used a washing liquid in the preceding filter and dilution liquid in the same filter. Normally, pure water is added to the last filter 18 as washing liquid, entering through a conduit 12.
  • Water is added to the last washing filter 18, this water being admixed with carbon dioxide and/or sulphur dioxide.
  • a pH sensor device may also be disposed in the conduit 28.

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Paper (AREA)

Abstract

Method in the washing of alkaline, cellulosic pulp, for example sulphate pulp, CTMP and CMP pulp, the washing being effected in at least one stage. By an addition of carbon dioxide, there will be realised greatly reduced washing losses of, primarily, inorganic ions, as well as improved washing-out of substances which give rise to chemical oxygen demand (COD).

Description

METHODFORWASHINGOFALCALINEPULP
TECHNICAL FIELD
The present invention relates to a method in the washin of alkaline, cellulosic pulp, the washing being effected in one or more consecutive stages.
In several processes within the cellulose industry, for instance in the manufacture of sulphate pulp and chemi-mecha ical pulp, immense volumes of relatively expensive chemicals are employed. In order that these processes be profitable, i is necessary that such treatment chemicals be recycled and regenerated as far as is possible. A further - and now stead ily more pressing - reason for the extensive recycling of treatment chemicals is the stringent requirements placed by central and local government authorities on low emissions of chemicals into the environment.
In order to attain washing results which answer to the requirements of such authorities, capital investment costs have had to be offset against running costs. As long as the price of energy was low, it was feasible to increase the vol ume of washing water, according as the requirements on wash effluent losses became stricter. It was then possible to eva orate the thus obtained large volumes of water. However, now that the price of energy is many times higher, concentrated efforts must be devoted to evolving more efficient washing equipment and more efficient washing processes which, to a considerable degree, free the pulp of its treatment chemi¬ cals.
OBJECTS OF THE PRESENT INVENTION
One object of the present invention is to reduce washing losses in the washing of alkaline pulp.
A further object of the present invention is to emascu¬ late alkaline, cellulosic pulp of sodium ions. A third obj ect of the present invention is to increase the washing-out , from alkaline, cell ulosic pulp, of substances which contribute to chemical oxygen demand (COD) .
SOLUTION
These objects are attained according to the present in¬ vention, in the washing of alkaline, cellulosic pulp, in that, during washing in one or more stages, the pH is lowered in the washing stage or at least one washing stage, the preferred agent added to the washing stage or several washing stages being carbon dioxide.
According to one embodiment of the present invention, the pH is lowered to approximately 9.
According to a further embodiment of the present inven¬ tion, the pH is lowered by carbon dioxide in one or more wash¬ ing stages, as a result of which there will be attained an improved washing-out from the pulp of substances which contri¬ bute to chemical oxygen demand (COD) .
The preferred agent for realising an improved washing of the pulp is carbon dioxide which is added to washing water used in the washing of the pulp and/or to the pulp suspension, prior to the washing stage. Possibly, carbon dioxide may also be added to the washing stage proper.
Carbon dioxide is the particularly preferred agent for attaining improved washing results. Carbon dioxide contains no environmentally hazardous substances such as chlorine or sul¬ phur.
However, in order to lower the pH, other acids may be added, for example sulphuric acid, which, granted, contains sulphur, since the pulp which is washed according to the pres¬ ent invention has been treated, prior to the washing - with sulphate-containing treatment liquid. If used, sulphuric acid is preferably added together with carbon dioxide in order to achieve a more manifest reduction of pH. This said, the pH should not be reduced overly much, since undersirable reac¬ tions with residual lignin may then occur. Above all, the pulp which can be washed with an additio of carbon dioxide or other pH reducing agent is sulphate pulp of softwood and deciduous or hardwood, and also chemi-mechani cal pulp, CTMP and CMP.
Since the washing operation is normally performed in several stages, the pH reducing agent is added in one or more stages, the agent not being added at least in the first wash¬ ing stage.
According to a particularly preferred embodiment of the present invention, the pH is reduced in the last stage of, fo example three or four washing stages, to approximately 5. In such instance, use may also be made, in addition to carbon dioxide, of a mineral acid, especially sulphuric acid.
BRIEF DESCRIPTION OF THE ACCOMPANYING DRAWINGS
The nature of the present invention and its aspects will be more readily understood from the following brief descrip¬ tion of the accompanying drawings, and discussion relating thereto.
In the accompanying drawings:
Fig. 1 is a schematic view of a laboratory plant for carrying the present invention into effect.
Fig. 2 is a schematic view of a laboratory plant for washing pulp countercurrently, and
Fig. 3 is a schematic view of a slightly modified plant for washing alkaline pulp in four stages.
DESCRIPTION OF PREFERRED EMBODIMENT
Referring to the drawings, reference numeral 51 in fig. designates a source for carbon dioxide which, by the inter¬ mediary of a conduit 57, is in communication with a rotameter 52, a manometer 53 and a vessel 54. The bottom 58 of the vessel 54 is a sintered body which finely divides the gas entering from the source 51. During the carbon dioxide addi¬ tion, the contents of the vessel 54 are agitated by means of an agitator 55 driven by a motor 56.
To 25 g of dry pulp, there was added 200 ml of black liquor. The mixture was left to stand for 48 hours. Thereafter, the mixture was diluted with deionised water to one litre, i.e. to a 2.5% pulp concentration. The suspension underwent agitation for one hour before the filtrate was removed. The pulp was then subjected to washing in four stages. In each stage, deionised water was added to a pulp concentration of 2.5%. Each washing stage lasted for one hour under agitation. All filtrates were kept for analysis. The amount of sodium in the washing water was determined using atom absorption and COD according to the Dr. Lange method.
In the accounted experimental series, carbon dioxide was added in the second washing stage during 5, 10, 20 and 40 minutes, respectively. The carbon dioxide flow was constant and uniform in all experiments. Because of the low degree of efficiency on the dissolution of carbon dioxide in these ex¬ periments, the quantity of CO- has not been calculated. In industrial and other plants, equipment well-known to the per¬ son skilled in the Art may readily dissolve the carbon dioxide in the washing water and pulp suspension.
It will be apparent from Table 1 that the total amount of washed-out sodium will be higher when CO- is added in the 2nd washing stage. The effect becomes manifest already in the stage where the carbon dioxide addition took place, i.e. the 2nd stage. Na is more effectively washed-out as a result of the pH reduction which results from addition of C0_.
The COD washing-out procedure is more complicated. Total amount of washed-out COD will be higher in an addition of CO,, in the 2nd washing stage. However, the effect is delayed and the improved washing effect does not become apparent until the 3rd washing stage.
It is not clear why the COD washing-out improves in this way. One possible explanation is of surface chemical nature. The following will then apply:
(RCOO) Ca →- RCOONa (RCOOH) resin and fatty acids
Figure imgf000006_0001
CaCO- is more sparingly soluble than (RCOO)-Ca Table 1
CO_ addition in 2nd washing stage (CO flow constant on addition)
CO, CO, CO, CO.
0 Sample 5 min 10 min 20 min 40 min
Na (tot)
Na (1) 1.14 1.26 1.23 1.18 3.28
Na (1+2)
Na (1) 1.10 1.21 1.19 1.16 1.22
Na (1+2+3)
Na (1) 1.13 1.25 1.21 1.17 1.24 pH (2) 10.8 7.5 7.4 7.2 5.7 pH (4) 9.4 7.6 7.8 7.6 7.1
COD (tot)
COD (1) 1.20 1.29 1.26 1.32 1.32
COD (1+2)
COD (1) 1.11 1.13 1.13 1.12 1.07
COD (1+2+3)
COD (1) 1.17 1.21 1.19 1.23 1.25
Na (tot) relates to the quotient of total washed-out Na and Na (1) washed-out Na in the first washing stage. Correspon¬ dingly the example below relates to
COD (1+2) COD washed out in first plus second stage through COD (1) COD washed out in stage 1.
No carbon dioxide was added in stage 1. pH(2) refers to pH after the second washing stage.
Calcium carbonate is deposited temporarily, calcium being "inactivated". Calcium soaps are insoluble in character and do not form lamellar phases to the same extent as sodium soaps. The surface activity in the system increases, which gives an improved washing-out of organic substance. A trial has been made to wash birch kraft pulp counter- currently on a laboratory scale. The purpose of this trial is to get closer to full scale conditions by using a counter- current method and to make this washing on birch kraft pulp having a higher extract content than pine kraft pulp.
The washing steps are schematically shown in figure 2. During steady state condition a batch of pulp suspension is supplied to the first washing, step 61, and washed by using the filtrate from the second step 62. The pulp washed in the first step is thereafter supplied to the second step 62 and washed with filtrate from the third step 63. The pulp washed in the second step thereafter is supplied to the third step in which said pulp is washed with filtrate from the fourth step 64. In the fourth step the pulp is washed with filtrate from the fifth step 65. In the fifth or last step 65 the pulp is washed with deionized water.
For the washing of each batch there was used a total amount of 700 ml deionized water as a washing liquid. The washing for each step was made in a graduated cylinder and the pulp suspension was agitated during several minutes. The pulp slurry then was filtered using a.Buechner funnel and 700 ml of filtrate was taken out.
For every batch of the pulp suspension 25 g of dry birch kraft pulp was mixed with 100 ml of black liquor. The suspen¬ sion was allowed to stand at least 2 days before the washing was started in step 61. During this time equilibrium condi¬ tions were reached or almost reached.
Two series of trials were made, one with carbon dioxide and one without carbon dioxide. In the first series no carbon dioxide was used.
In order to build up a steady state washing system 16 batches were washed in each series. Batch No. 1 was first washed in step 61 using 700 ml of deionized water, the ob¬ tained filtrate, 700 ml, was discarded. Batch No. 1 was then taken to step 62 and washed with 700 ml of deionized water. This obtained filtrate of 700 ml was taken care of and used as washing liquid in step 61 for batch No. 2. In the third washing step 63, of batch No. 1, the pulp was washed again with 700 ml of deionized water, the obtained filtrate, 700 ml, was taken care of and used as washing liquid for batc No. 2 in step 62. The filtrate from batch No. 2 in step 62 then was used as washing liquid in step 61 for batch No. 3. The filtrate, 700 ml, from step 1 was discarded. Then batch No. 1 was washed in step 64 with 700 ml of deionized water an finally in step 65 with 700 ml deionized water. The filtrate, 700 ml from batch No. 1 in step 65 then was used as washing liquid for the next batch. Thereafter deionized water was added only to step 65 and the filtrate from that step was use for washing the next batch in step 64, etc. The filtrate from step 61 for the 12 first batches was discarded. Then the last four filtrates from step 61 were taken care of, brought together to a comparative sample and analyzed.
In the second test series carbon dioxide was added to step 65. The carbon dioxide was added during the washing, which took some minutes and took place during stirring of the pulp suspension deionized water. The steady state condition was built up in the same manner as was done in the reference series without carbon dioxide. The last four filtrates from step 61 out of the 16 filtrates obtained were brought togethe and analyzed.
In addition, the pH of the filtrates from all steps was measured when the steady state condition had been reached. In the following, filtrate 61 designates filtrate from step 61, filtrate 62 designates filtrate from step 62, etc.
In table 2 the pH values of the filtrates after reaching steady state condition are shown. Table 2
Filtrate pH without C02 pH with C0_
65 10.3 6.8
64 10.6 9.4
63 11.0 10.9
62 11.6 11.8
61 12.1 12.6 Washed pulp, i.e. pulp from batches 12-16 were brought together to one sample, and filtrate 61 was analyzed f rther. Filtrate 61 designates the last four filtrates in each series containing 16 batches taken from step 61 brought together to an average sample. The results from the analysis of the fil¬ trate are shown in table 3.
Table 3 without CO- with CO-
Na+ (g/1) 3. 59 3 . 81
Ca2+ (g/1) 0. 033 0. 033
COD ( g/ 1) 17.1 17. 9
COD = Chemical oxygen demand
The results from the pulp analysis are shown in table 4.
Table 4 without co2 with CO-
Na+ ( g/kg) 2. 00 . 1 . 34
Ca2+ (g/kg) 1. 10 1. 17
COD ( g/kg) 10.19 9.37
DKM extr act ( % ) 0. 10 0. 08
DKM = dichloromethane
Addition of CO- to the last washing step has resulted in that more sodium ions and COD have been washed out of the pulp. The content of calcium ions has not been affected to any appreciable degree. The extractives content (dichloromethane) in the pulp is lower after washing with addition of carbon dioxide.
A modified plant for washing of pulp in sulphate cooking is illustrated in fig. 3
According to fig. 3 the pulp comes from a digester (not shown) through a conduit 1 to a blow tank 3. The conduit 2 leads to a blow condensor. The pulp in the blow tank 3 is diluted with weak (thin) liquor via a conduit 4 from a weak liquor cistern 19. An agitator in the blow tank 3 is desig¬ nated 5. The pulp from the blow tank 3 is passed through a condui 29 to a knotter screen 6. The pulp passes thence to the first washing filter 15 and subsequently to the three following washing filters 16, 17 and 18. The filtrate from the first filter 15 is collected in the weak liquor cistern 19 and the filtrate from the other three filters in the washing liquor cisterns 20, 21 and 22, respectively. The washed pulp departs from the fourth filter 18 at reference numeral 13. When the pulp passes from one filter to the next, the filter cake is comminuted by shredders 8. Filtrate from one filter is used a washing liquid in the preceding filter and dilution liquid in the same filter. Normally, pure water is added to the last filter 18 as washing liquid, entering through a conduit 12.
According to the present invention, carbon dioxide is introduced into the conduits 31 and/or 32 via conduits 23 and 24, respectively. The carbon dioxide dissolves at once in the washing liquid and is led to the filters 17 and 18, re¬ spectively through the conduits 31 and 32 and the conduits 10 and 11. The filtrate from the filter 16 passes through a con¬ duit 26 to the cistern 20. A pH sensor device is disposed either in the cistern 20 or in the conduit 26, the sensor controlling, by the intermediary of the control and regulatio equipment, the supply of carbon dioxide to the conduit 31. Correspondingly, there is disposed a pH sensor device in the conduit 27 or the cistern 21, this sensor being connected to control apparatus which maintains the pH at the predetermined level by adjusting the CO- addition via the conduit 24.
Water is added to the last washing filter 18, this water being admixed with carbon dioxide and/or sulphur dioxide. A pH sensor device may also be disposed in the conduit 28.
It has been found that it is possible to reduce the wash losses, counted as Na_S0., by approx. 1 kg per batched kg of carbon dioxide. A suitable amount of carbon dioxide is approx. 6 kg per tonne of pulp, it being thus possible to reduce the washing loss by approx. 6 kg per tonne of pulp. By further reducing the pH by an addition of a mineral acid, preferably sulphuric acid, and thus lowering the pH to 6 or less, even lower washing losses will be achieved.
In the manufacture of CTMP and CMP pulp, the cellulosic material is pre-treated with alkaline treatment liquid and is disintegrated in one or more refiners, normally disc refiners. The pulp suspension passes thence to a screen room. The accept therefrom then passes to a washing plant, for example of the type illustrated in fig. 3.
Using the method according the the present invention, it is possible to improve the washing results of all alkaline, cellulosic pulp, irrespective of whether the pulp is soft¬ wood/hardwood pulp or any other type of pulp, for example produced from bagasse.
The present invention should not be considered as re¬ stricted to that disclosed above and shown on the drawings, many modifications being conceivable without departing from the spirit and scope of the appended claims.

Claims

11CLAIMS
1. A method in the washing of alkaline, cellulosic pulp, in which the washing is effected in one or more consecutive stages, c h a r a c t e r i z e d in that the pH is lowered by carbon dioxide in the washing stage, or at least one wash¬ ing stage.
2. The method as claimed in Claim 1, c h a r a c t e r ¬ i z e* d in that the carbon dioxide is added to the washing water of the stage and/or the pulp suspension immediately prior to the washing stage.
3. The method as claimed in Claim 2, in which the washing is effected in at least two stages, c h a r a c t e r ¬ i z e d in that the carbon dioxide is added to all stages except the first stage.
4. The method as claimed in any one or more of Claim 1 to 3, c h a r a c t e r i z e d in that the pH is reduced to at least 9.
5. The method as claimed in Claim 4, c h a r a c t e r ¬ i z e d in that the pH is reduced to at least 7.
6. The method as claimed in Claim 5, c h a r a c t e r ¬ i z e d in that the pH is reduced to at least 5.
7. The method as claimed in any one or more of Claims 1 to 6 c h a r a c t e r i z e d in that the pulp is sulphate and/or chemi-mechanical (CTMP, CMP) pulp.
8. The method as claimed in Claim 3, c h a r a c t e r ¬ i z e d in that a mineral acid, preferably sulphuric acid, is also added to the last washing stage.
PCT/SE1987/000623 1986-12-22 1987-12-21 Method for washing of alcaline pulp Ceased WO1988004706A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
BR8707606A BR8707606A (en) 1986-12-22 1987-12-21 ALKALINE PULP WASHING PROCESS
JP63501165A JPH0778315B2 (en) 1986-12-22 1987-12-21 Cleaning method for alkaline pulp
AT88900488T ATE67536T1 (en) 1986-12-22 1987-12-21 METHOD OF WASHING AN ALKALINE PULP.
NO883736A NO172550C (en) 1986-12-22 1988-08-19 Method of washing alkaline cellulose pulp
FI883851A FI90256C (en) 1986-12-22 1988-08-19 Procedure for washing alkaline pulp

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
SE8605510A SE8605510L (en) 1986-12-22 1986-12-22 KEEP WASHING THE PASS
SE8605510-0 1986-12-22
SEPCT/SE87/00198 1987-04-16
PCT/SE1987/000198 WO1988004705A1 (en) 1986-12-22 1987-04-16 Method for washing of alcaline pulp

Publications (1)

Publication Number Publication Date
WO1988004706A1 true WO1988004706A1 (en) 1988-06-30

Family

ID=26659637

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/SE1987/000623 Ceased WO1988004706A1 (en) 1986-12-22 1987-12-21 Method for washing of alcaline pulp

Country Status (3)

Country Link
EP (1) EP0296198B1 (en)
DE (1) DE3773204D1 (en)
WO (1) WO1988004706A1 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5401362A (en) * 1993-03-24 1995-03-28 Kamyr, Inc. Control of metals and dissolved organics in the bleach plant
US5509999A (en) * 1993-03-24 1996-04-23 Kamyr, Inc. Treatment of bleach plant effluents
WO1999045202A1 (en) * 1998-03-03 1999-09-10 Aga Aktiebolag Improved papermaking processes
US6059925A (en) * 1994-11-14 2000-05-09 Aga Aktiebolag Method to regenerate gas mixture in ozone-bleaching process
US6126782A (en) * 1993-12-15 2000-10-03 Mo Och Domsjo Aktiebolag Method for non-chlorine bleaching of cellulose pulp with a totally closed counter-current liquid circuit
US6258208B1 (en) 1994-04-05 2001-07-10 Mo Och Domsjo Aktiebolag Method for complex treatment of pulp in conjunction with a chlorine dioxide stage
WO2001083886A1 (en) * 2000-05-04 2001-11-08 Aga Aktiebolag A process for controlling microbial growth
WO2008028960A1 (en) * 2006-09-08 2008-03-13 Linde Aktiengesellschaft Process for the deresination of pulp and use of carbon dioxide or (bi)carbonate therefor
WO2009003770A1 (en) * 2007-07-03 2009-01-08 Linde Aktiengesellschaft Process for making paper and use of an acid/base treatment in papermaking

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI991241A7 (en) 1999-06-01 2000-12-02 Aga Ab Lignin bleaching and method for making paper
US7056419B2 (en) 2002-09-30 2006-06-06 American Air Liquide, Inc. Methods for modifying electrical properties of papermaking compositions using carbon dioxide

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4042452A (en) * 1974-09-03 1977-08-16 A. Ahlstrom Osakeyhtio Process for washing cellulose pulp from alkali digestion wherein acid is added to the washing solution

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4042452A (en) * 1974-09-03 1977-08-16 A. Ahlstrom Osakeyhtio Process for washing cellulose pulp from alkali digestion wherein acid is added to the washing solution

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DERWENT'S ABSTRACT No 1980-18030C & SU,A,670 625 *
DERWENT'S ABSTRACT No 1980-91532C & SU,A,730 913 *

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5401362A (en) * 1993-03-24 1995-03-28 Kamyr, Inc. Control of metals and dissolved organics in the bleach plant
US5509999A (en) * 1993-03-24 1996-04-23 Kamyr, Inc. Treatment of bleach plant effluents
US6126782A (en) * 1993-12-15 2000-10-03 Mo Och Domsjo Aktiebolag Method for non-chlorine bleaching of cellulose pulp with a totally closed counter-current liquid circuit
US6258208B1 (en) 1994-04-05 2001-07-10 Mo Och Domsjo Aktiebolag Method for complex treatment of pulp in conjunction with a chlorine dioxide stage
US6059925A (en) * 1994-11-14 2000-05-09 Aga Aktiebolag Method to regenerate gas mixture in ozone-bleaching process
WO1999045202A1 (en) * 1998-03-03 1999-09-10 Aga Aktiebolag Improved papermaking processes
AU744905B2 (en) * 1998-03-03 2002-03-07 Aga Aktiebolag Improved papermaking processes
WO2001083886A1 (en) * 2000-05-04 2001-11-08 Aga Aktiebolag A process for controlling microbial growth
WO2008028960A1 (en) * 2006-09-08 2008-03-13 Linde Aktiengesellschaft Process for the deresination of pulp and use of carbon dioxide or (bi)carbonate therefor
WO2009003770A1 (en) * 2007-07-03 2009-01-08 Linde Aktiengesellschaft Process for making paper and use of an acid/base treatment in papermaking

Also Published As

Publication number Publication date
EP0296198B1 (en) 1991-09-18
EP0296198A1 (en) 1988-12-28
DE3773204D1 (en) 1991-10-24

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