EP2128331A1 - Processus de blanchiment de pâte à papier - Google Patents
Processus de blanchiment de pâte à papier Download PDFInfo
- Publication number
- EP2128331A1 EP2128331A1 EP08156934A EP08156934A EP2128331A1 EP 2128331 A1 EP2128331 A1 EP 2128331A1 EP 08156934 A EP08156934 A EP 08156934A EP 08156934 A EP08156934 A EP 08156934A EP 2128331 A1 EP2128331 A1 EP 2128331A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- bleaching
- process according
- pulp
- weight
- hydrogen peroxide
- 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.)
- Withdrawn
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- 238000004061 bleaching Methods 0.000 title claims abstract description 49
- 229920001131 Pulp (paper) Polymers 0.000 title claims abstract description 48
- 238000000034 method Methods 0.000 title claims abstract description 30
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 63
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims abstract description 18
- 239000000347 magnesium hydroxide Substances 0.000 claims abstract description 18
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims abstract description 18
- 150000003839 salts Chemical class 0.000 claims abstract description 14
- 239000000203 mixture Substances 0.000 claims abstract description 12
- FEWFXBUNENSNBQ-UHFFFAOYSA-N 2-hydroxyacrylic acid Chemical compound OC(=C)C(O)=O FEWFXBUNENSNBQ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000007900 aqueous suspension Substances 0.000 claims abstract description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 17
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 8
- 239000000920 calcium hydroxide Substances 0.000 claims description 8
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 8
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 claims description 7
- 229960003330 pentetic acid Drugs 0.000 claims description 7
- 239000004115 Sodium Silicate Substances 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 159000000000 sodium salts Chemical class 0.000 claims description 5
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 5
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 5
- RAEOEMDZDMCHJA-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-[2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]ethyl]amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CCN(CC(O)=O)CC(O)=O)CC(O)=O RAEOEMDZDMCHJA-UHFFFAOYSA-N 0.000 claims description 3
- RNMCCPMYXUKHAZ-UHFFFAOYSA-N 2-[3,3-diamino-1,2,2-tris(carboxymethyl)cyclohexyl]acetic acid Chemical compound NC1(N)CCCC(CC(O)=O)(CC(O)=O)C1(CC(O)=O)CC(O)=O RNMCCPMYXUKHAZ-UHFFFAOYSA-N 0.000 claims description 3
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 3
- 229960001484 edetic acid Drugs 0.000 claims description 3
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 2
- PDIZYYQQWUOPPK-UHFFFAOYSA-N acetic acid;2-(methylamino)acetic acid Chemical compound CC(O)=O.CC(O)=O.CNCC(O)=O PDIZYYQQWUOPPK-UHFFFAOYSA-N 0.000 claims description 2
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 claims description 2
- 229960001124 trientine Drugs 0.000 claims description 2
- 101000935117 Homo sapiens Voltage-dependent P/Q-type calcium channel subunit alpha-1A Proteins 0.000 description 14
- 208000036758 Postinfectious cerebellitis Diseases 0.000 description 14
- 102100025330 Voltage-dependent P/Q-type calcium channel subunit alpha-1A Human genes 0.000 description 14
- 150000002978 peroxides Chemical class 0.000 description 8
- 239000003381 stabilizer Substances 0.000 description 8
- 239000000725 suspension Substances 0.000 description 7
- 239000002738 chelating agent Substances 0.000 description 5
- 150000004679 hydroxides Chemical class 0.000 description 5
- 238000009897 hydrogen peroxide bleaching Methods 0.000 description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 3
- 241000218657 Picea Species 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229910052748 manganese Inorganic materials 0.000 description 3
- 239000011572 manganese Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 150000001455 metallic ions Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- -1 sodium hydroxide) Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Images
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
- D21C9/1026—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
- D21C9/1026—Other features in bleaching processes
- D21C9/1042—Use of chelating agents
Definitions
- the present invention relates to a process for the bleaching of paper pulp, especially mechanical paper pulp, through a bleaching treatment with hydrogen peroxide and an alkali source.
- Such bleaching treatment usually involves the use of peroxide stabilizers.
- the US patent 6221209 of SOLVAY INTEROX relates to a process for bleaching a chemical paper pulp by first purifying the pulp so as to reduce its manganese content and then by bleaching it with hydrogen peroxide in alkaline medium, especially at a pH adjusted to at least 10 by the addition of an alkaline compound (i.e. sodium hydroxide), and in the presence of a stabilizing agent, namely sodium silicate.
- an alkaline compound i.e. sodium hydroxide
- magnesium hydroxide is used as alkaline source in the hydrogen peroxide bleaching of mechanical paper pulp, it is difficult to achieve a satisfactory brightness, and the consumption of hydrogen peroxide for a given brightness is high.
- the purpose of the present invention is to provide a process which does not present the above disadvantages and which enables to obtain a higher paper pulp brightness compared to the known use of other alkaline sources than sodium hydroxide, such as magnesium hydroxide or calcium hydroxide.
- the purpose of the present invention is also to provide a process which allows decreasing the consumption of hydrogen peroxide for a given brightness.
- the present invention therefore relates to a process for the bleaching of paper pulp in which an aqueous suspension of paper pulp is subjected to a bleaching treatment with hydrogen peroxide in the presence of at least one alkaline earth hydroxide selected from magnesium hydroxide and calcium hydroxide and of at least one poly- ⁇ -hydroxyacrylic acid, its salt or their mixture.
- alkaline earth hydroxides such as magnesium hydroxide and/or calcium hydroxide as alkaline source
- sodium silicate cannot be used when using alkaline earth hydroxides such as magnesium hydroxide and/or calcium hydroxide as alkaline source, because it forms precipitates with those products, leading to scaling.
- Such scaling creates problems in the whole production line including in the paper machine, when the mill is an integrated site.
- alkaline earth hydroxides such as magnesium hydroxide and/or calcium hydroxide
- the common practice is to bleach without any stabilizer, except aminopolycarboxylic acids or their salts, such as diethylene triamine penta-acetic acid (DTPA) or its sodium salt which will act as chelating agents and will therefore limit the decomposition of the hydrogen peroxide which is catalyzed by transition metals such as manganese or iron.
- DTPA diethylene triamine penta-acetic acid
- the conditions present during the bleaching are usually not suitable for a good efficiency of such chelating agents and therefore the
- alkaline earth hydroxide selected from magnesium hydroxide and calcium hydroxide as alkaline source
- PHAA poly- ⁇ -hydroxyacrylic acid, its salt or their mixtures
- the PHAA used in the process of the invention generally has a molecular weight within a specific range. As the molecular weight is rather difficult to measure, it is inferred by measuring the viscosity, the higher the molecular weight, the higher the viscosity. Viscosity in the range of 10 to 100 mPa.s is usual but more particularly it can be in the range of 20 to 60 mPa.s. Commonly, the PHAA is used as a sodium salt of poly- ⁇ -hydroxyacrylic acid, corresponding to sodium poly- ⁇ -hydroxyacrylate (referred to as PHAS). In the invention, good results are obtained using only one PHAA. Nevertheless, more than one PHAA can be used.
- PHAS sodium poly- ⁇ -hydroxyacrylate
- the bleaching treatment according to the present invention is generally carried out at an initial pH of at least 8, in particular of at least 8,5, values of at least 9 being preferred.
- the initial pH is usually at most 14, in special cases at most 13, values of at most 12 being convenient.
- the pH of the aqueous suspension during the bleaching treatment is measured using equipment normally found in pulp mills for such a purpose.
- the natural pH of the paper pulp suspension is adjusted to the required value by means of an alkaline compound comprising at least one alkaline earth hydroxide selected from magnesium hydroxide and calcium hydroxide.
- the amount of alkaline earth hydroxide according to the invention, used in the bleaching step of the present invention is generally such that the pH of the suspension is maintained within the above-mentioned range. This amount is usually at least 0,1 % by weight of dry pulp, preferably at least 1% by weight of dry pulp, more preferably at least 2% by weight of dry pulp.
- the amount of alkaline earth hydroxide according to the invention, used in the bleaching step of the present invention is generally at most 10% by weight of dry pulp, with particular preference at most 5% by weight of dry pulp.
- the amount of alkaline earth hydroxide according to the invention, used in the bleaching step of the present invention is for instance of from 2 to 5% by weight of dry pulp, for example about 3% by weight of dry pulp.
- the amount of alkaline earth hydroxide according to the invention depends on the amount of hydrogen peroxide used and on the type of pulp.
- the ratio alkaline earth hydroxide according to the invention / hydrogen peroxide can for example vary from 0,3 to 2,5, preferably from 0,5 to 2,0 depending on the amount of hydrogen peroxide added and on the type of pulp. For example, the ratio may be about 1.
- the alkaline earth hydroxide according to the invention is usually added to the paper pulp suspension in the form of an aqueous slurry.
- the particle size of the alkaline earth hydroxide according to the invention is sufficiently small for the slurry to be readily suspendible, advantageously having a mean particle size of less than about 10 ⁇ m, preferably less than 6 ⁇ m, for example about 2 ⁇ m.
- the bleaching step of the invention is generally carried out at a consistency of at least 10 % of dry pulp based on the weight of pulp suspension.
- the efficiency of the process increases as the consistency is increased up to a value of around 30 % by weight of dry pulp.
- the consistency can be up to 40 % by weight of dry pulp.
- the bleaching treatment of the invention is usually carried out using an amount of hydrogen peroxide required to achieve the final target brightness.
- the amount of hydrogen peroxide is generally equal to or higher than 0,1 % by weight of dry pulp, preferably equal to or higher than 0,5 % by weight of dry pulp, more preferably equal to or higher than 1 % by weight of dry pulp.
- the amount of hydrogen peroxide is usually equal to or lower than 8 % by weight of dry pulp, especially equal to or lower than 6 % by weight of dry pulp, and more particularly equal to or lower than 5 % by weight of dry pulp.
- the amount of hydrogen peroxide may be about 2 to 4% by weight of dry pulp.
- the bleaching treatment of the invention is usually carried out at a temperature equal to or higher than 40°C, especially equal to or higher than 60°C.
- the temperature can be up to about 100°C.
- the temperature is preferably less than 100°C, more preferably equal to or less than 95°C, for example equal to or less than 85°C.
- the optimum bleach temperature depends on the wood type and pulping process but is normally in the range of 60 to 95°C.
- the duration of the bleaching treatment of the process of the invention is usually from 10 min to 6 h, varying from mill to mill. For instance, it can vary from 30 to 300 min.
- the bleaching treatment can be carried out at a pH of from 8 to 14, at a consistency of from 10 to 40 %, and at a temperature of from 60 to 95°C, during 1 to 4 hours.
- the amount of PHAA, especially PHAS, used in the bleaching step of the invention is usually equal to or higher than 0,05 % by weight of dry pulp, especially equal to or higher than 0,1 % by weight of dry pulp.
- the amount of PHAA is commonly equal to or lower than 2 % by weight of dry pulp, values of at most 1 % being suitable.
- typical amounts of PHAA are about 0,1 to 0,5 % by weight of dry pulp.
- the optimum amount is dependent on the amount of metallic ions in the pulp and must be optimized for each particular mill.
- the bleaching step of the invention can be carried out in the presence of any other alkaline or alkaline earth hydroxides than the alkaline earth hydroxides according to the invention, such as in the presence of sodium hydroxide.
- the bleaching step of the invention may also be carried out in the absence sodium hydroxide.
- the bleaching step of the invention can also be carried out in the presence of any other additives, such as magnesium sulfate or other soluble magnesium salts.
- the bleaching step is carried out in the absence of any other stabilizer, and especially in the absence of sodium silicate.
- the aqueous suspension of the paper pulp may be subjected to a chelating treatment to reduce the metallic ion content of the suspension, and especially its manganese content. It is for example usual to carry out a pretreatment step (or chelating treatment), with at least one aminopolycarboxylic acid, its salt or their mixture (referred to as APCA) prior to the bleaching treatment.
- a pretreatment step or chelating treatment
- APCA aminopolycarboxylic acid, its salt or their mixture
- the APCA used in the pretreatment step is generally chosen from ethylene diamine tetra-acetic acid (EDTA), diethylene triamine penta-acetic acid (DTPA), triethylene tetramine hexa-acetic acid (TTHA), cyclohexane diamine tetra-acetic acid (CDTA), methylglycine di-acetic acid (MGDA), nitrilo tri-acetic acid (NTA).
- EDTA ethylene diamine tetra-acetic acid
- DTPA diethylene triamine penta-acetic acid
- TTHA triethylene tetramine hexa-acetic acid
- CDTA cyclohexane diamine tetra-acetic acid
- MGDA methylglycine di-acetic acid
- NTA nitrilo tri-acetic acid
- the APCA may be used as the free acid, its salt or their mixtures.
- the APCA is preferably used as its salt.
- the most preferred APCA is the sodium salt of DTPA. Good results are generally obtained using only one APCA. Nevertheless, more than one APCA can be used.
- the chelating pretreatment step may be conducted as described in the International patent application filed as EP2008/052056 , the text of which is incorporated herein by reference.
- the bleaching treatment may be carried out in the presence of at least one chelating agent, in particular of at least one APCA, such as those disclosed above.
- the amount of APCA used in the bleaching treatment of the invention is usually at least 0,05 % wt based on the weight of dry pulp.
- the amount of APCA is commonly at most about 1 % wt based on the weight of dry pulp, values of at most 0,8 % wt being suitable.
- the weight ratio between PHAA, especially PHAS, and APCA is usually at least 1:10, preferably at least 1:5, ratios of at least 1:3 being satisfactory.
- the weight ratio PHAA / APCA, especially PHAS / APCA is generally at most 10:1, especially at most 5:1, values of at most 3:1 1 giving the best results.
- the bleaching treatment is carried out in the absence of a chelating agent or of another stabilizer than PHAA.
- the paper pulp treated in the present invention can be chosen from chemical paper pulps, mechanical paper pulps or recycled paper pulps. The best results are obtained with mechanical paper pulps.
- mechanical paper pulps are meant paper pulps obtained by mechanical treatment. Examples of such paper pulps are pressure groundwood (PGW), stone groundwood (SGW), thermomechanical pulp (TMP), refiner mechanical pulp (RMP), chemithermomechanical pulp (CTMP) and alkaline peroxide mechanical pulp (APMP or APP).
- PGW pressure groundwood
- SGW stone groundwood
- TMP thermomechanical pulp
- RMP refiner mechanical pulp
- CTMP chemithermomechanical pulp
- APMP or APP alkaline peroxide mechanical pulp
- the present invention therefore also relates to the bleaching process of the invention applied to mechanical paper pulp.
- the process of the invention can further comprise other treatment steps such as one or more additional dilution step(s), one or more additional chelating step(s), one or more additional bleaching step(s), one or more washing step(s) and/or one or more extraction step(s).
- the order of addition of the alkaline earth hydroxide of the invention, the PHAA and the hydrogen peroxide is either first the PHAA, then the alkaline earth hydroxide of the invention, and lastly the hydrogen peroxide or first the alkaline earth hydroxide of the invention, then the PHAA, and lastly the hydrogen peroxide.
- Those three products may also be premixed all together or two of them can be premixed.
- the alkaline earth of the invention is usually added as a suspension in water. Dilution water may also be added.
- the reactants are introduced in the paper pulp suspension via a pump and a high consistency mixer, especially when the bleaching is performed at a consistency close to 30%.
- An example of configuration is : the chemicals are added in the preheating screw of the HC mixer.
- example 2 the same conditions as in example 1 were applied except that 0,5% of PHAS were added to the bleaching step.
- the resulting brightness of the paper pulp was 76,6°ISO and the residual peroxide content was 17% of the initial charge.
- example 4 the same mechanical pulp as in example 3 was bleached at 70°C during 2 hours in the presence of an amount of hydrogen peroxide of 2 % by weight of dry pulp, of magnesium hydroxide of 3 % by weight of dry pulp, and of an amount of PHAS of 0,3 % by weight of dry pulp.
- the resulting brightness of the paper pulp was the same as in example 3 (73,8°ISO) and the residual peroxide content was 31 % of the initial charge.
- Hydrogen peroxide was added in an amount of 3 % by weight of dry pulp.
- Magnesium hydroxide was added in an amount of 3 % by weight of dry pulp.
- PHAS was added in an amount of 0 to 0,5 % by weight of dry pulp.
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Paper (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08156934A EP2128331A1 (fr) | 2008-05-26 | 2008-05-26 | Processus de blanchiment de pâte à papier |
| US12/992,316 US20110067831A1 (en) | 2008-05-26 | 2009-05-25 | Process for the bleaching of paper pulp |
| PCT/EP2009/056278 WO2009144190A1 (fr) | 2008-05-26 | 2009-05-25 | Procédé de blanchiment de la pâte à papier |
| CA2723311A CA2723311A1 (fr) | 2008-05-26 | 2009-05-25 | Procede de blanchiment de la pate a papier |
| EP09753845A EP2286024A1 (fr) | 2008-05-26 | 2009-05-25 | Procédé de blanchiment de la pâte à papier |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08156934A EP2128331A1 (fr) | 2008-05-26 | 2008-05-26 | Processus de blanchiment de pâte à papier |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2128331A1 true EP2128331A1 (fr) | 2009-12-02 |
Family
ID=39878001
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP08156934A Withdrawn EP2128331A1 (fr) | 2008-05-26 | 2008-05-26 | Processus de blanchiment de pâte à papier |
| EP09753845A Withdrawn EP2286024A1 (fr) | 2008-05-26 | 2009-05-25 | Procédé de blanchiment de la pâte à papier |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP09753845A Withdrawn EP2286024A1 (fr) | 2008-05-26 | 2009-05-25 | Procédé de blanchiment de la pâte à papier |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20110067831A1 (fr) |
| EP (2) | EP2128331A1 (fr) |
| CA (1) | CA2723311A1 (fr) |
| WO (1) | WO2009144190A1 (fr) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010136550A1 (fr) * | 2009-05-29 | 2010-12-02 | Solvay Sa | Procédé de blanchiment de pâte à papier mécanique |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0801169A1 (fr) * | 1996-04-12 | 1997-10-15 | Elf Atochem S.A. | Procédé de délignification et de blanchiment de pâtes à papier chimiques |
| DE19614587A1 (de) * | 1996-04-13 | 1997-10-16 | Jaschinski Thomas Dipl Holzw | Verfahren und Bleichlösung zum Bleichen von cellulosischen Faserstoffen |
| EP0814193A2 (fr) * | 1996-06-21 | 1997-12-29 | Nippon Peroxide Co., Ltd. | Agent stabilisateur pour le blanchiment au peroxyde et procédés pour le blanchiment d'un matériau fibreux l'utilisant |
| US6221209B1 (en) | 1992-07-06 | 2001-04-24 | Solvay Interox (Société Anonyme) | Multi-stage bleaching process having a final stabilized peroxide stage |
| US20010050153A1 (en) * | 2000-01-28 | 2001-12-13 | Wajer Mark T. | Process employing magnesium hydroxide in peroxide bleaching of mechanical pulp |
| US20050217813A1 (en) * | 2004-03-31 | 2005-10-06 | Shevchenko Sergey M | Methods to enhance brightness of pulp and optimize use of bleaching chemicals |
| WO2005108673A1 (fr) * | 2004-05-12 | 2005-11-17 | Kemira Oyj | Composition et procede pour le traitement d'une matiere fibreuse |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1978129B (zh) * | 2005-12-02 | 2010-11-10 | 鸿富锦精密工业(深圳)有限公司 | 滚圆设备 |
| FI119375B (fi) * | 2007-02-02 | 2008-10-31 | Kemira Oyj | Uusi koostumus ja menetelmä kuitumateriaalin käsittelemiseksi |
-
2008
- 2008-05-26 EP EP08156934A patent/EP2128331A1/fr not_active Withdrawn
-
2009
- 2009-05-25 EP EP09753845A patent/EP2286024A1/fr not_active Withdrawn
- 2009-05-25 CA CA2723311A patent/CA2723311A1/fr not_active Abandoned
- 2009-05-25 WO PCT/EP2009/056278 patent/WO2009144190A1/fr not_active Ceased
- 2009-05-25 US US12/992,316 patent/US20110067831A1/en not_active Abandoned
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6221209B1 (en) | 1992-07-06 | 2001-04-24 | Solvay Interox (Société Anonyme) | Multi-stage bleaching process having a final stabilized peroxide stage |
| EP0801169A1 (fr) * | 1996-04-12 | 1997-10-15 | Elf Atochem S.A. | Procédé de délignification et de blanchiment de pâtes à papier chimiques |
| DE19614587A1 (de) * | 1996-04-13 | 1997-10-16 | Jaschinski Thomas Dipl Holzw | Verfahren und Bleichlösung zum Bleichen von cellulosischen Faserstoffen |
| EP0814193A2 (fr) * | 1996-06-21 | 1997-12-29 | Nippon Peroxide Co., Ltd. | Agent stabilisateur pour le blanchiment au peroxyde et procédés pour le blanchiment d'un matériau fibreux l'utilisant |
| US20010050153A1 (en) * | 2000-01-28 | 2001-12-13 | Wajer Mark T. | Process employing magnesium hydroxide in peroxide bleaching of mechanical pulp |
| US7052578B2 (en) | 2000-01-28 | 2006-05-30 | Martin Marietta Magnesia Specialties, Inc. | Process employing magnesium hydroxide in peroxide bleaching of mechanical pulp |
| US20050217813A1 (en) * | 2004-03-31 | 2005-10-06 | Shevchenko Sergey M | Methods to enhance brightness of pulp and optimize use of bleaching chemicals |
| WO2005108673A1 (fr) * | 2004-05-12 | 2005-11-17 | Kemira Oyj | Composition et procede pour le traitement d'une matiere fibreuse |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010136550A1 (fr) * | 2009-05-29 | 2010-12-02 | Solvay Sa | Procédé de blanchiment de pâte à papier mécanique |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2009144190A1 (fr) | 2009-12-03 |
| EP2286024A1 (fr) | 2011-02-23 |
| CA2723311A1 (fr) | 2009-12-03 |
| US20110067831A1 (en) | 2011-03-24 |
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