WO2002075046A1 - Bleaching of pulp with chlorine dioxide - Google Patents

Bleaching of pulp with chlorine dioxide Download PDF

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Publication number
WO2002075046A1
WO2002075046A1 PCT/SE2002/000287 SE0200287W WO02075046A1 WO 2002075046 A1 WO2002075046 A1 WO 2002075046A1 SE 0200287 W SE0200287 W SE 0200287W WO 02075046 A1 WO02075046 A1 WO 02075046A1
Authority
WO
WIPO (PCT)
Prior art keywords
pulp
chlorine dioxide
bleaching
stage
concentration
Prior art date
Application number
PCT/SE2002/000287
Other languages
French (fr)
Inventor
Ann-Sofi NÄSHOLM
Original Assignee
Metso Paper, Inc
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 Metso Paper, Inc filed Critical Metso Paper, Inc
Priority to US10/472,297 priority Critical patent/US20040112556A1/en
Priority to CA2435813A priority patent/CA2435813C/en
Priority to AT0904102A priority patent/AT412482B/en
Publication of WO2002075046A1 publication Critical patent/WO2002075046A1/en
Priority to FI20031338A priority patent/FI120652B/en

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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
    • D21C9/12—Bleaching ; Apparatus therefor with halogens or halogen-containing compounds
    • D21C9/14—Bleaching ; Apparatus therefor with halogens or halogen-containing compounds with ClO2 or chlorites
    • D21C9/144—Bleaching ; Apparatus therefor with halogens or halogen-containing compounds with ClO2 or chlorites with ClO2/Cl2 and other bleaching agents in a multistage process

Definitions

  • the present invention relates to a method for efficient and economical end-bleaching with chlorine dioxide wherein the method relates to a method for end bleaching of pulp containing metal ions after a sequence comprising alkaline bleaching stages only and optionally treatment with complex forming agent, wherein the end-bleaching comprises two chlorine dioxide steps with intermediate wash and alkali extraction where the chlorine dioxide stages are performed at a pulp concentration of 8-20% and pH 2.5-4.5 wherein the pulp after the first chlorine dioxide steps is washed and dewatered to a concentration of 12-50% for removal of out-dissolved metal ions and that alkali thereupon is added to the pulp for extraction and fast increase of pH to 8-14, whereupon the pulp is provided with acid and chlorine dioxide and is introduced into the second chlorine dioxide step.
  • end bleaching of chemical pulp is performed with chlorine dioxide, see for instance SE 466 062.
  • an extraction stage (E) that is an alkalisation of the pulp, and/or with a wash between the stages. If there is no separate extraction stage alkali may be added in order to raise the pH, during the dilution at the end of the first chlorine dioxide tower before the pulp is washed.
  • a short alkalisation/neutralisation step (n) results in that chlorine dioxide bleaching in the following chlorine dioxide stage will be more efficient (see for instance Papermaking Science and Technology, Book 6A, Chemical Pulping, Editor J. Gullichsen and H. Paulapuro, page A642) .
  • SE 98000797-4 describes a bleaching method for cooked and oxygen delignified pulp where you make use of a commencing acid bleaching stage which is followed by a washing stage at an even lower pH than in the bleaching stage from which washing stage a filtrate is taken out .
  • the purpose here is to bring metals, which forms difficultly dissolvable compounds, into solution so that they may be removed in the washing stage . Accordingly the degree of closing for the following bleaching may be increased.
  • the present invention solves the above problems through providing a method which minimises the risk for precipitations during two-step chlorine dioxide bleaching with intermediate short alkali extraction, in which the alkalisation of the pulp suspension is performed after a dewatering step, including wash of the pulp, wherein the out-dissolved metals are separated in the wash-/dewatering equipment.
  • the wash/dewatering execution is preferably performed in a wash/dewatering press. That is the sequence will be after an alkaline pre-bleaching: D-dewatering (including wash)-nD.
  • a further advantage with the invention is that a less amount of alkali is consumed, as a smaller liquid amount is to be alkalised at high pulp concentration.
  • the present invention relates to a method for end- bleaching of pulp containing metal ions after a sequence comprising alkaline bleaching stages only and optionally treatment with complex forming agent, wherein the end- bleaching comprises two chlorine dioxide stages at a pulp concentration of 8-20% and pH 2.5-4.5, with intermediate wash and alkali extraction, wherein the pulp after the first chlorine dioxide stage is washed and dewatered to a concentration of 12-50% for removal of out-dissolved metal ions, and that alkali thereupon is added to the pulp for extraction and fast increase of pH to 8-14, whereupon the pulp is provided with acid and chlorine dioxide and introduced into the second chlorine dioxide stage .
  • pulp is intended to embrace in the present description preferably chemical pulp, which may be soft wood pulp or hard wood pulp or mixtures thereof .
  • the chemical pulp is achieved through the fibre freeing being performed in a chemical way; for instance it may be bleached pulp from both soft wood (softwood) and pulp from hard wood (hardwood) .
  • acid is intended to embrace in the present description an acid which may be selected from the group consisting of sulphuric acid, hydrochloric acid, nitric acid, sulphur dioxide, acetic acid or carbonic acid or a combination of these .
  • ozone hydrogen peroxide, hypo chlorite or alkali. If the pulp has high consistency ozone may be preferred.
  • the pulp is de-watered after the first chlorine dioxide stage to a concentration of 25-50%, preferably 30-40%.
  • the chlorine dioxide stages are performed at a pulp concentration of 8-15%, preferably 10-12%.
  • Chlorine dioxide which is used, is preferably in the form of a water solution. Further the bleaching is preferably performed in an acid environment, pH 2.5 to 4.5. According to a preferred embodiment of the present invention the fast increase of pH in the method, during the alkali extraction, is performed to a pH 8-14, preferably 9-12, most preferred pH 9-11.
  • the in-going pulp has medium consistency (normally 8 to 20% pulp concentration; so called MC-pulp) and the de-watered pulp after the first end-bleaching stage with chlorine dioxide, high consistency (normally 25 to 50% pulp concentration; so called HC-pulp) .
  • the pulp is diluted and dewatered, including wash of the pulp, after the first chlorine dioxide stage wherein an acid outflow with high metal content is obtained from .the pulp whereupon the pulp is diluted with alkalised filtrate so that pH is increased to >8 , preferably from pH 8 to 14, before the pulp is provided with chlorine dioxide and acid for the second chlorine dioxide stage .
  • the acid- and chlorine dioxide addition is performed before the second chlorine dioxide stage 15 seconds to 5 minutes, preferably 30 seconds to 2 minutes after the alkali addition.
  • the treatment with complex forming agent has been performed in a pH interval from 4.5 to 10, preferably from 4.5 to 7 before the end-bleaching.
  • the concentration of the pulp is performed in an apparatus for washing and dewatering in the method, for instance by using a wash-press or a press, preferably a wash- press or a dewatering press.
  • a pump preferably is used or a corresponding apparatus .
  • Figure 1 shows a principal sketch where the method according to the invention is illuminated in the form of a system for end bleaching by using chlorine dioxide wherein said method may be performed.
  • the method for end bleaching according to the present invention may be performed through the following:
  • Pulp which has been bleached in alkaline bleaching stages and which has been treated with complex forming agent is transported to a first chlorine dioxide (C10 2 ) reactor whereupon the pulp is diluted and washed.
  • the initial pulp may have a pH of 8-12
  • This washing may be performed by using a concentration apparatus as set out in the description before, preferably by using a wash-press or a dewatering- press.
  • a metal rich drainage is removed during the washing of the pulp.
  • the pulp has essentially a higher consistency, preferably high consistency.
  • the pulp is then quickly diluted to the earlier consistency with dilution liquid, which contains sodium hydroxide (NaOH) , wherein a fast alkali extraction is achieved.
  • Acid for regulation of pH and C10 2 is added in connection with the introduction into the second reactor, which is included in the end-bleaching phase for the pulp.

Abstract

The present invention relates to a method for end-bleaching of pulp containing metal ions after a sequence comprising alkaline bleaching stages only and optionally treatment with complex forming agent, wherein the end-bleaching comprises two chlorine dioxide stages at a pulp concentration of 8-20 % and pH 2.5-4.5 wherein the pulp after the first chlorine dioxide stage is washed and dewatered to a concentration of 12-50 % for removal of the out-dissolved metal ions and that alkali thereupon is added to the pulp for fast alkali extraction and increase of pH to 8-14, whereupon the pulp is provided with acid and chlorine dioxide and introduced into the second chlorine dioxide stage.

Description

B l each i ng of pu l p w i th ch l or i ne d i ox i de .
TECHNICAL FIELD
The present invention relates to a method for efficient and economical end-bleaching with chlorine dioxide wherein the method relates to a method for end bleaching of pulp containing metal ions after a sequence comprising alkaline bleaching stages only and optionally treatment with complex forming agent, wherein the end-bleaching comprises two chlorine dioxide steps with intermediate wash and alkali extraction where the chlorine dioxide stages are performed at a pulp concentration of 8-20% and pH 2.5-4.5 wherein the pulp after the first chlorine dioxide steps is washed and dewatered to a concentration of 12-50% for removal of out-dissolved metal ions and that alkali thereupon is added to the pulp for extraction and fast increase of pH to 8-14, whereupon the pulp is provided with acid and chlorine dioxide and is introduced into the second chlorine dioxide step.
BACKGROUND OF THE TECHNOLOGY
It is common that end bleaching of chemical pulp is performed with chlorine dioxide, see for instance SE 466 062. In most of the cases it is performed in two steps with an extraction stage (E) , that is an alkalisation of the pulp, and/or with a wash between the stages. If there is no separate extraction stage alkali may be added in order to raise the pH, during the dilution at the end of the first chlorine dioxide tower before the pulp is washed. A short alkalisation/neutralisation step (n) results in that chlorine dioxide bleaching in the following chlorine dioxide stage will be more efficient (see for instance Papermaking Science and Technology, Book 6A, Chemical Pulping, Editor J. Gullichsen and H. Paulapuro, page A642) . When alkali is added to the chlorine dioxide bleached pulp lignin is out-dissolved which would, if not out-washed before the following chlorine dioxide stage, consume bleaching chemicals or result in a lower end- brightness. Therefore two-stage chlorine dioxide bleaching is presently performed with intermediate neutralisation stage according to the Dn-Wash-D. Further, SE 98000797-4 describes a bleaching method for cooked and oxygen delignified pulp where you make use of a commencing acid bleaching stage which is followed by a washing stage at an even lower pH than in the bleaching stage from which washing stage a filtrate is taken out . The purpose here is to bring metals, which forms difficultly dissolvable compounds, into solution so that they may be removed in the washing stage . Accordingly the degree of closing for the following bleaching may be increased.
PROBLEMS WITH THE PRESENT TECHNOLOGY
Concurrently with the bleach plants being closed even harder and pre-bleaching is preferably performed in alkaline stages (for instance O, 00, (OP), (PO) , (EO) , (EOP) ) and complex forming agent stage (Q) the overcarry of metals with the pulp to the end-bleaching increases, as they have not been washed out in any acid stage. This results in that the risk for precipitations increases if the pulp is taken into an acid stage for end bleaching which it does in a chlorine dioxide stage, D-stage. If the manufacture of pulp is performed in alkaline bleaching stages and complex forming agent stage and the end-bleaching in D-stage the metals are out-dissolved in the surrounding liquid in the acid D-stage. When the pulp thereupon is alkalised the conditions in the pulp suspension becomes favourable for precipitations, above all for calcium compounds. An example of one such calcium compound is calcium oxalate, which may form a china-resembling precipitation, which may be very difficult to remove from process equipment. A change in pH in a pulp suspension where the pulp concentration is approximately 10-15% gives a gradual change of pH, which may result in that the pH interval for precipitations (~ pH 4-9) is reached. If the pulp could have a high dry substance content, ds>25% before the pH adjustment and dilution, a quick and stepwise change of pH from acid conditions to alkaline conditions could be performed and critical conditions for precipitation would therewith be avoided .
SUMMARY OF THE INVENTION
The present invention solves the above problems through providing a method which minimises the risk for precipitations during two-step chlorine dioxide bleaching with intermediate short alkali extraction, in which the alkalisation of the pulp suspension is performed after a dewatering step, including wash of the pulp, wherein the out-dissolved metals are separated in the wash-/dewatering equipment. The wash/dewatering execution is preferably performed in a wash/dewatering press. That is the sequence will be after an alkaline pre-bleaching: D-dewatering (including wash)-nD. A further advantage with the invention is that a less amount of alkali is consumed, as a smaller liquid amount is to be alkalised at high pulp concentration. Further pH gradients may be avoided as the dilution with alkaline filtrate is performed when the pulp essentially has a higher consistency, preferably high consistency. The present invention relates to a method for end- bleaching of pulp containing metal ions after a sequence comprising alkaline bleaching stages only and optionally treatment with complex forming agent, wherein the end- bleaching comprises two chlorine dioxide stages at a pulp concentration of 8-20% and pH 2.5-4.5, with intermediate wash and alkali extraction, wherein the pulp after the first chlorine dioxide stage is washed and dewatered to a concentration of 12-50% for removal of out-dissolved metal ions, and that alkali thereupon is added to the pulp for extraction and fast increase of pH to 8-14, whereupon the pulp is provided with acid and chlorine dioxide and introduced into the second chlorine dioxide stage .
DETAILED DESCRIPTION OF THE INVENTION The expression "pulp" is intended to embrace in the present description preferably chemical pulp, which may be soft wood pulp or hard wood pulp or mixtures thereof . The chemical pulp is achieved through the fibre freeing being performed in a chemical way; for instance it may be bleached pulp from both soft wood (softwood) and pulp from hard wood (hardwood) .
The expression "acid" is intended to embrace in the present description an acid which may be selected from the group consisting of sulphuric acid, hydrochloric acid, nitric acid, sulphur dioxide, acetic acid or carbonic acid or a combination of these .
Other chemicals which may be used in connection with chlorine dioxide bleaching is ozone, hydrogen peroxide, hypo chlorite or alkali. If the pulp has high consistency ozone may be preferred.
According to a preferred embodiment of the present invention the pulp is de-watered after the first chlorine dioxide stage to a concentration of 25-50%, preferably 30-40%. According to a preferred embodiment of the present invention the chlorine dioxide stages are performed at a pulp concentration of 8-15%, preferably 10-12%.
Chlorine dioxide, which is used, is preferably in the form of a water solution. Further the bleaching is preferably performed in an acid environment, pH 2.5 to 4.5. According to a preferred embodiment of the present invention the fast increase of pH in the method, during the alkali extraction, is performed to a pH 8-14, preferably 9-12, most preferred pH 9-11.
According to a preferred embodiment of the present inven- tion the in-going pulp has medium consistency (normally 8 to 20% pulp concentration; so called MC-pulp) and the de-watered pulp after the first end-bleaching stage with chlorine dioxide, high consistency (normally 25 to 50% pulp concentration; so called HC-pulp) . According to a preferred embodiment of the present invention the pulp is diluted and dewatered, including wash of the pulp, after the first chlorine dioxide stage wherein an acid outflow with high metal content is obtained from .the pulp whereupon the pulp is diluted with alkalised filtrate so that pH is increased to >8 , preferably from pH 8 to 14, before the pulp is provided with chlorine dioxide and acid for the second chlorine dioxide stage .
According to a preferred embodiment of the present invention the acid- and chlorine dioxide addition is performed before the second chlorine dioxide stage 15 seconds to 5 minutes, preferably 30 seconds to 2 minutes after the alkali addition.
According to a preferred embodiment of the present invention the treatment with complex forming agent has been performed in a pH interval from 4.5 to 10, preferably from 4.5 to 7 before the end-bleaching.
According to a preferred embodiment of the present invention the concentration of the pulp is performed in an apparatus for washing and dewatering in the method, for instance by using a wash-press or a press, preferably a wash- press or a dewatering press. In order to convey (transport) the pulp between the reactors further a pump preferably is used or a corresponding apparatus .
We will now in more details describe the present invention by use of figures and example and these shall only be regarded as illuminating and not in any way limiting for the invention as it is set out in the appended set of claims. DESCRIPTIONS OF FIGURE
Figure 1 shows a principal sketch where the method according to the invention is illuminated in the form of a system for end bleaching by using chlorine dioxide wherein said method may be performed.
EXAMPLE
As can be seen in figure 1 the method for end bleaching according to the present invention may be performed through the following:
Pulp which has been bleached in alkaline bleaching stages and which has been treated with complex forming agent is transported to a first chlorine dioxide (C102) reactor whereupon the pulp is diluted and washed. (The initial pulp may have a pH of 8-12) . This washing may be performed by using a concentration apparatus as set out in the description before, preferably by using a wash-press or a dewatering- press. A metal rich drainage is removed during the washing of the pulp. At this moment the pulp has essentially a higher consistency, preferably high consistency. The pulp is then quickly diluted to the earlier consistency with dilution liquid, which contains sodium hydroxide (NaOH) , wherein a fast alkali extraction is achieved. Acid for regulation of pH and C102 is added in connection with the introduction into the second reactor, which is included in the end-bleaching phase for the pulp.
The invention is of course not limited to the showed embodiment but may be varied within the frame of the spirit of the invention.

Claims

1. A method for end bleaching of pulp containing metal ions after a sequence comprising alkaline bleaching stages only and optionally treatment with complex forming agent, wherein the end bleaching comprises two chlorine dioxide steps at a pulp concentration of 8-20% and pH 2.5-4.5 characterized by that the pulp after the first chlorine dioxide stage is washed and dewatered to a concentration of 12-50% for removal of out-dissolved metal ions, and that alkali thereupon is added to the pulp for extraction and fast increase of pH to 8- 14, whereupon the pulp is provided with acid and chlorine dioxide and is introduced into the second chlorine dioxide step, wherein the pulp after the first chlorine dioxide stage is dewatered to a concentration of 25-50%.
2. A method according to claim 1 characterized by that the pulp after the first chlorine dioxide stage is dewatered to a concentration of 30-40%.
3. A method according to claim 1 characterized by that the fast increase of pH is performed to pH 9-12, preferably pH 9-11.
4. A method according to claim 1 characterized by that the pulp is chemical pulp.
5. A method according to claim 1 characterized by that the acid and chlorine dioxide addition before the second chlorine dioxide stage is performed 15 seconds to 5 minutes, preferably 30 seconds to 2 minutes after the alkali addition.
6. A method according claim 1 characterized by that the treatment with complex forming agent has been done in a pH interval from 4.5 to 10, preferably from 4.5 to 7.
PCT/SE2002/000287 2001-03-20 2002-02-19 Bleaching of pulp with chlorine dioxide WO2002075046A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US10/472,297 US20040112556A1 (en) 2001-03-20 2002-02-19 Bleaching of pulp with chlorine dioxide
CA2435813A CA2435813C (en) 2001-03-20 2002-02-19 Bleaching of pulp with chlorine dioxide after alkaline bleaching
AT0904102A AT412482B (en) 2001-03-20 2002-02-19 BLEACHING POWDER WITH CHLORIDE DIOXIDE
FI20031338A FI120652B (en) 2001-03-20 2003-09-18 Process for the final bleaching of a metal ion-containing pulp with chlorine dioxide

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0100977A SE518692C2 (en) 2001-03-20 2001-03-20 Bleaching of pulp with chlorine dioxide
SE0100977-8 2001-03-20

Publications (1)

Publication Number Publication Date
WO2002075046A1 true WO2002075046A1 (en) 2002-09-26

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PCT/SE2002/000287 WO2002075046A1 (en) 2001-03-20 2002-02-19 Bleaching of pulp with chlorine dioxide

Country Status (6)

Country Link
US (1) US20040112556A1 (en)
AT (1) AT412482B (en)
CA (1) CA2435813C (en)
FI (1) FI120652B (en)
SE (1) SE518692C2 (en)
WO (1) WO2002075046A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008076268A2 (en) * 2006-12-18 2008-06-26 International Paper Company A process in a (d) stage bleaching of hardwood pulps in a presence of mg(oh)2
WO2008076267A2 (en) * 2006-12-18 2008-06-26 International Paper Company A process in a (d) stage bleaching of softwood pulps in a presence of mg(oh)2
WO2009108111A1 (en) * 2008-02-28 2009-09-03 Metso Paper, Inc. Method of bleaching a pulp

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EP3262490A4 (en) * 2015-02-23 2018-10-17 Somniq, Inc. Empathetic user interface, systems, and methods for interfacing with empathetic computing device

Citations (1)

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Publication number Priority date Publication date Assignee Title
WO1991017306A1 (en) * 1990-04-30 1991-11-14 Sunds Defibrator Industries Aktiebolag Bleaching of chemical pulp

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US4238281A (en) * 1979-04-30 1980-12-09 Canadian International Paper Company Simplified bleaching process
US5938892A (en) * 1991-01-28 1999-08-17 Champion International Corporation Process for recycling bleach plant filtrate
US6706143B1 (en) * 1996-03-19 2004-03-16 International Paper Company Minimizing chlorinated organics in pulp bleaching processes
US6475338B1 (en) * 1996-06-05 2002-11-05 Andritz Inc. Method of minimizing transition metal ions during chemical pulping in a digester by adding chelating agent to the digester

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Publication number Priority date Publication date Assignee Title
WO1991017306A1 (en) * 1990-04-30 1991-11-14 Sunds Defibrator Industries Aktiebolag Bleaching of chemical pulp

Non-Patent Citations (1)

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Title
JOHAN GULLICHSEN ET AL.: "Papermaking science and technology, book 6A", 2000, FAPET, OY, PO BOX 146, FIN-00171 HELSINKI, FINLAND, XP002950213 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008076268A2 (en) * 2006-12-18 2008-06-26 International Paper Company A process in a (d) stage bleaching of hardwood pulps in a presence of mg(oh)2
WO2008076267A2 (en) * 2006-12-18 2008-06-26 International Paper Company A process in a (d) stage bleaching of softwood pulps in a presence of mg(oh)2
WO2008076267A3 (en) * 2006-12-18 2008-08-14 Int Paper Co A process in a (d) stage bleaching of softwood pulps in a presence of mg(oh)2
WO2008076268A3 (en) * 2006-12-18 2008-09-18 Int Paper Co A process in a (d) stage bleaching of hardwood pulps in a presence of mg(oh)2
US7976677B2 (en) 2006-12-18 2011-07-12 International Paper Company Process of bleaching hardwood pulps in a D1 or D2 stage in a presence of a weak base
US7976676B2 (en) 2006-12-18 2011-07-12 International Paper Company Process of bleaching softwood pulps in a D1 or D2 stage in a presence of a weak base
WO2009108111A1 (en) * 2008-02-28 2009-09-03 Metso Paper, Inc. Method of bleaching a pulp
US8257550B2 (en) 2008-02-28 2012-09-04 Metso Paper, Inc. Method of bleaching a pulp

Also Published As

Publication number Publication date
CA2435813A1 (en) 2002-09-26
AT412482B (en) 2005-03-25
FI120652B (en) 2010-01-15
SE0100977L (en) 2002-09-21
CA2435813C (en) 2010-04-27
SE518692C2 (en) 2002-11-05
FI20031338A (en) 2003-09-18
US20040112556A1 (en) 2004-06-17
ATA90412002A (en) 2004-08-15
SE0100977D0 (en) 2001-03-20

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