EP0679760B1 - Process for bleaching of lignocellulose-containing pulp - Google Patents
Process for bleaching of lignocellulose-containing pulp Download PDFInfo
- Publication number
- EP0679760B1 EP0679760B1 EP94203640A EP94203640A EP0679760B1 EP 0679760 B1 EP0679760 B1 EP 0679760B1 EP 94203640 A EP94203640 A EP 94203640A EP 94203640 A EP94203640 A EP 94203640A EP 0679760 B1 EP0679760 B1 EP 0679760B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- pulp
- magnesium
- calcium
- compound
- chlorine
- 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
Links
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
- D21C9/16—Bleaching ; Apparatus therefor with per compounds
- D21C9/163—Bleaching ; Apparatus therefor with per compounds with peroxides
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/1005—Pretreatment of the pulp, e.g. degassing the pulp
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/1026—Other features in bleaching processes
- D21C9/1036—Use of compounds accelerating or improving the efficiency of the processes
-
- 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
- D21C9/147—Bleaching ; Apparatus therefor with oxygen or its allotropic modifications
- D21C9/153—Bleaching ; Apparatus therefor with oxygen or its allotropic modifications with ozone
Definitions
- the present invention relates to a process for delignification and bleaching of chemically digested lignocellulose-containing pulp, wherein the pulp is acid treated at a pH of between about 1 and about 6, whereupon a water-soluble mixture of a magnesium compound and a calcium compound is added at a pH of between about 1 and about 7 before the pulp is treated with a chlorine-free bleaching agent comprising hydrogen peroxide at a pH of from about 8 up to about 12.
- the initial acidic treatment removes the trace metals of the pulp, whereas the subsequent addition of alkaline earth metal ions in aqueous solution returns the ions to the positions in the pulp where they have a particularly beneficial effect on the preservation of the cellulose chains and, consequently, on the viscosity, as well as on the consumption of bleaching agent in the subsequent bleaching step.
- the pulp may be finally bleached to the desired brightness, suitably with a chlorine-free bleaching agent, such a ozone, to completely avoid formation and discharge of AOX.
- chlorine-free bleaching agents such as hydrogen peroxide, peracetic acid or ozone
- the delignification and consumption of the bleaching agent become less effective than with chlorine-containing bleaching agents, unless the pulp is pretreated.
- a hydrogen peroxide treatment in an alkaline environment is disturbed by the presence in the pulp of ions of certain metals, such as Mn, Cu and Fe. These metal ions cause degradation of hydrogen peroxide, thereby reducing the efficiency of the peroxide treatment and increasing the consumption of peroxide.
- this can be counteracted by pretreating the pulp with an acid, such as sulphuric acid or nitric acid, whereby the concentration of all types of metal ions is reduced.
- an acid such as sulphuric acid or nitric acid
- metal ions for example Mg, which are advantageous to the peroxide treatment disappear, which ions stabilize the peroxide and increase the selectivity of the peroxide.
- CA-A-575,636 discloses the addition of magnesium sulphate to stabilize alkaline peroxide solutions. However, the addition is made directly to the bleaching liquor and in alkaline environment insoluble magnesium hydroxide precipitates.
- EP-A-0 148 712 teaches to bleach chemical cellulose pulp with hydrogen peroxide in one step at a pH of 11 to 11,5.
- the peroxide bleach solution comprises a salt of magnesium and a salt of calcium which are kept in solution by means of a complexing agent.
- US-A-4,222,819 discloses the addition of magnesium ions to acidic peroxide solutions, but also in this case the addition is made directly to the bleaching liquor. None of the related methods makes possible diffusion of the magnesium ions into the pulp to such an extent, that a pulp of high brightness and strength can be obtained.
- the invention provides a process in which lignocellulose-containing pulp is treated under the conditions disclosed in the claims, whereby the metal ions harmful to the subsequent bleaching are effectively removed and the profile of alkaline earth metals is restored before the pulp is bleached in a chlorine-free bleaching step.
- the invention relates to a process for bleaching of chemically digested lignocellulose-containing pulp, wherein the pulp is acid treated at a pH in the range from about 1 up to about 6, whereupon the pulp is washed and a mixture containing a magnesium compound and a calcium compound is added at a pH in the range from about 1 up to about 7 and in an amount of from about 0.01 kg, suitably 0.5 kg, up to about 10 kg/ton of dry pulp, calculated as magnesium and calcium, and that the pulp subsequently is treated with a chlorine-free bleaching agent comprising hydrogen peroxide at a pH of from about 8 up to about 12.
- Acid treatment is an effective process to eliminate metal ions from lignocellulose-containing pulps.
- ions of magnesium and calcium especially when in their original positions in the pulp, have a positive influence on the selectivity of the delignification as well as on the stability and consumption of chlorine-free bleaching agents, such as peroxides, ozone and oxygen.
- the present process presents an economic solution to the problem of creating a suitable trace-metal profile for the subsequent chlorine-free bleaching, in that non-desirable metal ions are eliminated while supplied ions of magnesium and calcium essentially recover the positions in the vicinity of the cellulose chains previously occupied by ions of alkaline earth metals.
- an advantage of the present process is that the pH adjustment between the treatment with acid and addition of alkaline earth metal ions becomes very limited or may be left out altogether, which is advantageous to process technique and economy.
- Chlorine-free bleaching agents include inorganic peroxide compounds, such as hydrogen peroxide and sodium peroxide, organic peroxide compounds, such as peracetic acid, as well as ozone, oxygen and sodium dithionite.
- hydrogen peroxide (P), oxygen (O) and ozone (Z) are used in an optional sequence or mixture.
- the sequence P-Z or (PO)-Z are especially preferred.
- pH is suitably adjusted by adding to the pulp an alkali or an alkali-containing liquid, such as sodium carbonate, sodium hydrogen carbonate, sodium hydroxide, oxidized white liquor or magnesium hydroxide slurry.
- an alkali or an alkali-containing liquid such as sodium carbonate, sodium hydrogen carbonate, sodium hydroxide, oxidized white liquor or magnesium hydroxide slurry.
- the magnesium hydroxide slurry is taken from the chemical handling system in the production of sulphite pulp with magnesium as base, i.e. magnefite pulp.
- the acid treatment suitably is carried out with an acid.
- the acids used are inorganic acids, suitably sulphuric acid, nitric acid, hydrochloric acid or residual acid from a chlorine dioxide reactor, either separately or in an optional mixture.
- sulphuric acid is employed.
- magnesium-containing compounds such as magnesium sulphate or magnesium chloride
- calcium-containing compounds such as calcium chloride or calcium oxide.
- the acid treatment is carried out at a pH of from about 1 up to about 6, suitably from 1.5 up to 5, preferably from 2 up to 4. It is especially preferred that the acid treatment is carried out at a pH of from 2 up to 3.
- Magnesium is one of the alkaline earth metals in the compounds containing an alkaline earth metal.
- the addition is made at a pH in the range from about 1 up to about 7, suitably in the range from 2 up to 6, preferably in the range from 2 up to 4. It is especially preferred that the addition of magnesium is made at a pH of from 2 up to 3.
- the chlorine-free bleaching agent is hydrogen peroxide
- the pulp is treated at a pH of from about 8 up to about 12, preferably at a pH of from 10 up to 12. Treatment with the other chlorine-free bleaching agents mentioned above, is carried out within the same pH range.
- the treatment according to the invention is carried out with a washing step between the acid treatment and addition of alkaline earth metal ions, such that the trace metals that are harmful to the treatment with a chlorine-free bleaching agent are removed from the pulp suspension.
- a mixture of a magnesium compound and a calcium compound and a chlorine-free bleaching agent can be carried out at an optional position in the bleaching sequence, e.g. immediately after digestion of the pulp or after an oxygen step.
- the process according to the invention is preferably applied to pulp that has been delignified in an oxygen step prior to the treatment.
- the pulp in the acid treatment also can be subjected to bleaching and/or delignifying treatment.
- Bleaching and/or delignifying chemicals active within the pH range suitable in the acid treatment are e.g. chlorine dioxide, ozone, peracetic acid and/or an acid peroxide-containing compound.
- a combination of acid treatment and bleaching and/or delignifying treatment takes place in an ozone step.
- Lignocellulose-containing pulps relate to chemical pulps of softwood and/or hardwood digested according to the sulphite, sulphate, soda or organosolv process, or modifications and/or combinations thereof.
- Use is suitably made of softwood and/or hardwood digested according to the sulphate process, preferably sulphate pulp of hardwood.
- the treatment according to the invention can be applied to lignocellulose-containing pulps having an initial kappa number within the range from about 5 up to about 40, suitably 7 up to 32, preferably from 10 up to 20.
- the kappa number is determined according to the standard method SCAN-C 1:77.
- the acid treatment is carried out at a temperature of from about 10 up to about 95°C, suitably from 20 up to 80°C and preferably from 40 up to 80°C, and for a period of time of from about 1 up to about 120 min, suitably from 10 up to 120 min and preferably from 20 up to 40 min.
- the mixture of a magnesium compound and a calcium compound is added at a temperature of from about 10 up to about 95°C, preferably from 40 up to 80°C, and for a period of time of from about 1 up to about 180 min, preferably from 20 up to 180 min and preferably from 30 up to 120 min.
- the pulp is treated at a temperature of from about 30 up to about 100°C, preferably from 60 up to 90°C, and for a period of time of from about 30 up to about 300 min, suitably from 60 up to 240 min.
- the pulp concentration may be from about 3 up to about 35% by weight, preferably from 3 up to 15% by weight.
- the pulp concentration may be from about 3 up to about 50% by weight, suitably from 3 up to 35% by weight and preferably from 10 up to 25% by weight.
- Treatment with the other chlorine-free bleaching agents mentioned above is carried out within the normal ranges of temperature, time and pulp concentration for each bleaching agent, which are well-known to the person skilled in the art.
- the amount of mixture containing a magnesium compound and a calcium compound charged lies in the range from about 0.5 up to about 10 kg/ton of dry pulp, suitably in the range from 0.5 up to 5 kg/ton of dry pulp, and preferably in the range from 2 up to 4 kg/ton of dry pulp, calculated as magnesium and calcium.
- the amount of hydrogen peroxide lies in the range from about 2 up to about 50 kg/ton of dry pulp, calculated as 100% hydrogen peroxide.
- the upper limit is not critical, but has been set for reasons of economy.
- the amount of hydrogen peroxide suitably lies in the range from 3 up to 30 kg/ton of dry pulp and preferably from 4 up to 20 kg/ton of dry pulp, calculated as 100% hydrogen peroxide.
- the pulp can be used for direct production of paper with a lower demand of brightness.
- the pulp may be finally bleached to the desired higher brightness, by treatment in one or more steps.
- the final bleaching is also carried out with chlorine-free bleaching agents of the type mentioned above, optionally with intermediate alkaline extraction steps, which may be reinforced with peroxide and/or oxygen. In this way, the formation and discharge of AOX is completely eliminated.
- the final bleaching is carried out with ozone in one or more steps.
- the lignin content has been reduced to a sufficiently low level before any chlorine-containing bleaching agents are used. Therefore, chlorine dioxide and/or hypochlorite may well be used in one or more final bleaching steps without causing formation of large amounts of AOX.
- the process according to the invention means that the brightness and kappa number of the resulting pulp is higher and lower, respectively, than with the processes in which a mixture of a magnesium compound and a calcium compound is not added at all or is added at a higher pH.
- the aim is a high brightness as well as a low kappa number, the latter meaning a low content of undissolved lignin.
- the consumption of the chlorine-free bleaching agent should be as low as possible meaning lower treatment costs.
- these objects are met.
- the strength of the pulp measured as viscosity, is sufficient, which means that the pulp contains cellulose chains which are long enough to give a strong product.
- Sulphate pulp of softwood having a kappa number of 17, a brightness of 35% ISO and a viscosity of 970 dm 3 /kg was treated with sulphuric acid at a pH of 2.0.
- the pulp was treated at a temperature of 60°C for 30 min, the pulp concentration being 10% by weight.
- magnesium was added in the form of an aqueous solution containing MgSO 4 , to give a concentration of magnesium in the pulp of at least 500 ppm.
- the pH at the time of the addition was varied between 2.3 and 11.5 by addition of sulphuric acid.
- the pulp was bleached with hydrogen peroxide at a temperature of 90°C, the residence time and pulp concentration being 180 min and 15% by weight, respectively.
- the final pH was 11.5, and the addition of hydrogen peroxide was 15 kg/ton of dry pulp, calculated as 100% hydrogen peroxide.
- magnesium was added directly to the hydrogen peroxide step under the conditions stated above, in accordance with the prior art.
- the pulp was also treated with only sulphuric acid and hydrogen peroxide under the conditions stated above.
- the kappa number, viscosity and brightness of the pulp were determined according to SCAN Standard Methods, and the consumption of hydrogen peroxide was determined by iodometric titration. The test results appear from the Table below.
- the treatment with MgSO 4 at a pH in the range from about 2 up to about 6 is essential to give maximum increase in brightness and maximum reduction of the kappa number, as well as minimum decrease in viscosity and minimum consumption of hydrogen peroxide. Furthermore, the importance of the magnesium ions for the increase in brightness appears from the comparison at a pH of 2.3, where, in the final test, the peroxide treatment was preceded only by acidic treatment.
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- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Paper (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Noodles (AREA)
- Diaphragms For Electromechanical Transducers (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Stringed Musical Instruments (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Materials For Medical Uses (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
Abstract
Description
pH at the addition of Mg | Kappa number step 2 | Viscosity step 2 (dm3/kg) | Brightness step 2 (% ISO) | Residual H2O step 2 (kg/ton) |
2.3 | 9.1 | 903 | 61.0 | 1.5 |
4.7 | 9.2 | 910 | 60.0 | 1.0 |
9.5 | 9.8 | 930 | 56.1 | 0.9 |
11.5 | 10.0 | 940 | 52.2 | 0.2 |
---- | 9.8 | 890 | 54.1 | 0.5 |
2.3 | 9.9 | 875 | 48.2 | 0.0 |
Claims (9)
- A process for delignification and bleaching of chemically digested lignocellulose-containing pulp, during which the pulp is acid treated at a pH in the range from about 1 up to about 6 and the pulp is washed after the acid treatment, characterised in that thereafter a water-soluble mixture of a magnesium compound and a calcium compound is added at a pH in the range from about 1 up to about 7 and in an amount of from about 0.5 up to about 10 kg/ton of dry pulp, calculated as magnesium and calcium, and that subsequently the pulp is delignified and bleached with a chlorine-free bleaching agent comprising hydrogen peroxide at a pH of from about 8 up to about 12.
- A process according to claim 1, characterised in that the water-soluble mixture of a magnesium compound and a calcium compound is added in an amount of from about 2 up to about 10 kg/ton of dry pulp, calculated as magnesium and calcium.
- A process according to claim 1, characterised in that the chemically digested pulp is a sulphate pulp.
- A process according to claim 1, characterised in that the water-soluble mixture of a magnesium compound and a calcium compound is added at a pH of from 2 up to 6.
- A process according to claim 1, characterised in that the calcium compound is calcium chloride or calcium oxide.
- A process according to claim 1 or 5, characterised in that magnesium compound is magnesium sulphate or magnesium chloride.
- A process according to claim 1, characterised in that the chlorine-free bleaching agent consists of oxygen and hydrogen peroxide.
- A process according to claim 7, characterised in that the pulp, after the treatment, is finally bleached with ozone in one or more steps.
- A process according to claims 1-8, characterised in that the acid treatment is carried out at a temperature of from about 10 up to about 95°C for about 1 up to about 120 min, that the mixture of a magnesium compound and a calcium compound is added at a temperature of from about 10 up to about 95°C for about 1 up to about 180 min and in an amount of from 0.5 up to 5 kg/ton of dry pulp, calculated as magnesium compound and calcium compound, the treated pulp having a concentration of from about 3 up to about 35% by weight, and that the pulp is bleached and delignified with hydrogen peroxide at a pH of from about 8 up to about 12.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE9101301 | 1991-04-30 | ||
SE9101301A SE470065C (en) | 1991-04-30 | 1991-04-30 | Treatment of chemical pulp with an acid and then a magnesium and calcium compound in chlorine-free bleaching |
EP92201005A EP0511695B2 (en) | 1991-04-30 | 1992-04-08 | Process for bleaching of lignocellulose-containing pulp |
Related Parent Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP92201005.3 Division | 1992-04-08 | ||
EP92201005A Division EP0511695B2 (en) | 1991-04-30 | 1992-04-08 | Process for bleaching of lignocellulose-containing pulp |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0679760A1 EP0679760A1 (en) | 1995-11-02 |
EP0679760B1 true EP0679760B1 (en) | 1998-11-18 |
Family
ID=20382601
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP94203640A Expired - Lifetime EP0679760B1 (en) | 1991-04-30 | 1992-04-08 | Process for bleaching of lignocellulose-containing pulp |
EP92201005A Expired - Lifetime EP0511695B2 (en) | 1991-04-30 | 1992-04-08 | Process for bleaching of lignocellulose-containing pulp |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP92201005A Expired - Lifetime EP0511695B2 (en) | 1991-04-30 | 1992-04-08 | Process for bleaching of lignocellulose-containing pulp |
Country Status (14)
Country | Link |
---|---|
EP (2) | EP0679760B1 (en) |
JP (1) | JP2592747B2 (en) |
AT (2) | ATE141971T1 (en) |
BR (1) | BR9201554A (en) |
CA (1) | CA2067296C (en) |
DE (2) | DE69213080D1 (en) |
ES (1) | ES2091395T3 (en) |
FI (1) | FI111964B (en) |
MX (1) | MX9201966A (en) |
NO (1) | NO180495C (en) |
NZ (1) | NZ242465A (en) |
RU (1) | RU2039141C1 (en) |
SE (1) | SE470065C (en) |
ZA (1) | ZA923073B (en) |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FI89516B (en) | 1989-05-10 | 1993-06-30 | Ahlstroem Oy | Foerfarande Foer blekning av cellulosamassa med Otson |
US6398908B1 (en) | 1991-04-30 | 2002-06-04 | Eka Nobel Ab | Process for acid bleaching of lignocellulose-containing pulp with a magnesium compound |
SE500353C2 (en) * | 1992-10-26 | 1994-06-06 | Sca Wifsta Oestrand Ab | Peroxide bleaching of sulfate pulp with the addition of magnesium before bleaching |
SE512137C2 (en) * | 1992-10-29 | 2000-01-31 | Eka Chemicals Ab | Process for bleaching lignocellulosic pulp |
SE9203366L (en) * | 1992-11-11 | 1994-05-12 | Mo Och Domsjoe Ab | Process for delignification and / or bleaching of cellulose pulp |
US6007678A (en) * | 1992-11-27 | 1999-12-28 | Eka Nobel Ab | Process for delignification of lignocellulose-containing pulp with an organic peracid or salts thereof |
DE69420306T2 (en) * | 1993-04-20 | 2000-04-20 | Eka Chemicals Ab | Process for bleaching lignocellulosic pulp |
SE500616C2 (en) * | 1993-06-08 | 1994-07-25 | Kvaerner Pulping Tech | Bleaching of chemical pulp with peroxide at overpressure |
US6605181B1 (en) * | 1993-10-01 | 2003-08-12 | Kvaerner Pulping Aktiebolag | Peroxide bleach sequence including an acidic bleach stage and including a wash stage |
BE1007757A3 (en) * | 1993-11-10 | 1995-10-17 | Solvay Interox | Method of laundering of chemical pulp. |
US6776876B1 (en) | 1994-10-13 | 2004-08-17 | Andritz Oy | Method of treating cellulosic pulp to remove hexenuronic acid |
FI102301B1 (en) * | 1994-10-13 | 1998-11-13 | Ahlstrom Machinery Oy | Process for treating cellulose pulp |
DE19516151A1 (en) * | 1995-05-03 | 1996-11-07 | Sven Siegle | Process for the production of a pulp from cellulosic material, the pulp itself and its use |
FI105701B (en) * | 1995-10-20 | 2000-09-29 | Ahlstrom Machinery Oy | Method and arrangement for treatment of pulp |
JPH108092A (en) * | 1996-06-21 | 1998-01-13 | Mitsubishi Paper Mills Ltd | Stabilizer for peroxide bleaching treatment and bleaching of fibrous substance with the same |
BE1010679A3 (en) * | 1996-10-11 | 1998-11-03 | Solvay Interox | Delignification process and laundering pulp chemicals. |
ID23571A (en) * | 1997-08-25 | 2000-05-04 | Praxair Technology Inc | METHOD OF OZONE APPLICATION IN ECF BLEACHING |
JP2002266272A (en) * | 2001-03-12 | 2002-09-18 | Nippon Paper Industries Co Ltd | Method for bleaching cellulosic fibrous material pulp |
US6743332B2 (en) * | 2001-05-16 | 2004-06-01 | Weyerhaeuser Company | High temperature peroxide bleaching of mechanical pulps |
KR100547491B1 (en) * | 2005-04-27 | 2006-01-31 | 이권혁 | The production method and pulp maked bamboos |
US9512237B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Method for inhibiting the growth of microbes with a modified cellulose fiber |
US9512563B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Surface treated modified cellulose from chemical kraft fiber and methods of making and using same |
US9511167B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
JP5799009B2 (en) | 2009-05-28 | 2015-10-21 | ゲーペー ツェルローゼ ゲーエムベーハー | Modified cellulose derived from chemical kraft fibers and methods of making and using the same |
BR112013030060A2 (en) | 2011-05-23 | 2018-01-16 | Gp Cellulose Gmbh | kraft resin wood fibers and board and their method for making kraft fiber |
EP3800290B1 (en) | 2012-01-12 | 2023-11-01 | GP Cellulose GmbH | A low viscosity kraft fiber having reduced yellowing properties and methods of making and using the same |
WO2013158384A1 (en) | 2012-04-18 | 2013-10-24 | Georgia-Pacific Consumer Products Lp | The use of surfactant to treat pulp and improve the incorporation of kraft pulp into fiber for the production of viscose and other secondary fiber products |
US9115468B2 (en) * | 2012-09-27 | 2015-08-25 | Andritz Inc. | Chemical treatment of lignocellulosic fiber bundle material, and methods and systems relating thereto |
BR112015018492A2 (en) | 2013-02-08 | 2017-07-18 | Gp Cellulose Gmbh | kraft fiber and method for making oxidized kraft pulp |
KR102330233B1 (en) | 2013-03-14 | 2021-11-23 | 게페 첼루로제 게엠베하 | A method of making a highly functional, low viscosity kraft fiber using an acidic bleaching sequence and a fiber made by the process |
WO2014140940A2 (en) | 2013-03-15 | 2014-09-18 | Gp Cellulose Gmbh | A low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same |
CN107709657A (en) * | 2015-09-30 | 2018-02-16 | 伊梅里斯矿物有限公司 | The method of belaching aqueous paper pulp and the composition for these methods |
WO2018093697A1 (en) | 2016-11-16 | 2018-05-24 | Gp Cellulose Gmbh | Modified cellulose from chemical fiber and methods of making and using the same |
WO2021209586A1 (en) * | 2020-04-16 | 2021-10-21 | Bim Kemi Ab | Delignification process |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1206704A (en) * | 1982-01-28 | 1986-07-02 | Dominique Lachenal | Treatment of chemical pulp |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3507744A (en) * | 1966-04-01 | 1970-04-21 | Kimberly Clark Co | Wood pulp bleaching process utilizing peroxide pyrophosphate high concentration compositions |
SE335053B (en) * | 1969-05-13 | 1971-05-10 | Mo Och Domsjoe Ab | |
DE2742262C2 (en) * | 1977-09-20 | 1982-06-09 | Degussa Ag, 6000 Frankfurt | Process for the production of a medium to high viscosity softwood sulphite pulp |
FR2557605B1 (en) * | 1983-12-29 | 1987-12-11 | Atochem | PROCESS FOR BLEACHING PAPER PULP BY HYDROGEN PEROXIDE |
JPH0364589A (en) * | 1989-07-28 | 1991-03-19 | Mitsubishi Gas Chem Co Inc | Bleaching of chemical pulp |
-
1991
- 1991-04-30 SE SE9101301A patent/SE470065C/en not_active IP Right Cessation
-
1992
- 1992-04-08 ES ES92201005T patent/ES2091395T3/en not_active Expired - Lifetime
- 1992-04-08 EP EP94203640A patent/EP0679760B1/en not_active Expired - Lifetime
- 1992-04-08 AT AT92201005T patent/ATE141971T1/en not_active IP Right Cessation
- 1992-04-08 EP EP92201005A patent/EP0511695B2/en not_active Expired - Lifetime
- 1992-04-08 DE DE69213080T patent/DE69213080D1/en not_active Expired - Lifetime
- 1992-04-08 AT AT94203640T patent/ATE173518T1/en not_active IP Right Cessation
- 1992-04-08 DE DE69227640T patent/DE69227640T2/en not_active Expired - Fee Related
- 1992-04-23 NZ NZ242465A patent/NZ242465A/en unknown
- 1992-04-27 FI FI921886A patent/FI111964B/en active
- 1992-04-27 CA CA002067296A patent/CA2067296C/en not_active Expired - Fee Related
- 1992-04-28 MX MX9201966A patent/MX9201966A/en unknown
- 1992-04-28 ZA ZA923073A patent/ZA923073B/en unknown
- 1992-04-28 JP JP4134325A patent/JP2592747B2/en not_active Expired - Fee Related
- 1992-04-28 BR BR929201554A patent/BR9201554A/en not_active IP Right Cessation
- 1992-04-29 RU SU925011770A patent/RU2039141C1/en not_active IP Right Cessation
- 1992-04-29 NO NO19921671A patent/NO180495C/en not_active IP Right Cessation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1206704A (en) * | 1982-01-28 | 1986-07-02 | Dominique Lachenal | Treatment of chemical pulp |
Non-Patent Citations (1)
Title |
---|
J.P. CASEY: "Pulp and Paper; Chemistry and Chemical Technology, 3rd edition, vol. I, page 651", JOHN WILEY & SONS, NEW YORK * |
Also Published As
Publication number | Publication date |
---|---|
NO921671L (en) | 1992-11-02 |
MX9201966A (en) | 1992-11-01 |
JPH05148784A (en) | 1993-06-15 |
SE470065C (en) | 1996-01-15 |
JP2592747B2 (en) | 1997-03-19 |
NZ242465A (en) | 1993-12-23 |
SE470065B (en) | 1993-11-01 |
BR9201554A (en) | 1992-12-01 |
EP0511695B1 (en) | 1996-08-28 |
AU651192B2 (en) | 1994-07-14 |
ATE141971T1 (en) | 1996-09-15 |
ATE173518T1 (en) | 1998-12-15 |
CA2067296C (en) | 1997-03-04 |
EP0511695A1 (en) | 1992-11-04 |
EP0511695B2 (en) | 2004-06-02 |
SE9101301D0 (en) | 1991-04-30 |
ES2091395T3 (en) | 1996-11-01 |
NO921671D0 (en) | 1992-04-29 |
EP0679760A1 (en) | 1995-11-02 |
FI921886A (en) | 1992-10-31 |
DE69213080D1 (en) | 1996-10-02 |
NO180495B (en) | 1997-01-20 |
ZA923073B (en) | 1992-12-30 |
RU2039141C1 (en) | 1995-07-09 |
FI111964B (en) | 2003-10-15 |
AU1514992A (en) | 1993-03-11 |
DE69227640T2 (en) | 1999-05-06 |
DE69227640D1 (en) | 1998-12-24 |
NO180495C (en) | 2003-06-06 |
CA2067296A1 (en) | 1992-10-31 |
SE9101301L (en) | 1992-10-31 |
FI921886A0 (en) | 1992-04-27 |
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