WO1996027046A1 - Method and apparatus for making paper pulp using basic processing effluents from a hydrogen peroxide production plant - Google Patents

Method and apparatus for making paper pulp using basic processing effluents from a hydrogen peroxide production plant Download PDF

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Publication number
WO1996027046A1
WO1996027046A1 PCT/FR1996/000302 FR9600302W WO9627046A1 WO 1996027046 A1 WO1996027046 A1 WO 1996027046A1 FR 9600302 W FR9600302 W FR 9600302W WO 9627046 A1 WO9627046 A1 WO 9627046A1
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WO
WIPO (PCT)
Prior art keywords
hydrogen peroxide
solution
basic
paper pulp
pulp
Prior art date
Application number
PCT/FR1996/000302
Other languages
French (fr)
Inventor
Henry Ledon
Original Assignee
Chemoxal S.A.
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 Chemoxal S.A. filed Critical Chemoxal S.A.
Publication of WO1996027046A1 publication Critical patent/WO1996027046A1/en

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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
    • D21C9/10Bleaching ; Apparatus therefor
    • D21C9/16Bleaching ; Apparatus therefor with per compounds
    • D21C9/163Bleaching ; Apparatus therefor with per compounds with peroxides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B15/00Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
    • C01B15/01Hydrogen peroxide
    • C01B15/022Preparation from organic compounds
    • C01B15/023Preparation from organic compounds by the alkyl-anthraquinone process
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B15/00Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
    • C01B15/01Hydrogen peroxide
    • C01B15/037Stabilisation by additives
    • 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
    • D21C11/00Regeneration of pulp liquors or effluent waste waters
    • D21C11/0021Introduction of various effluents, e.g. waste waters, into the pulping, recovery and regeneration cycle (closed-cycle)

Definitions

  • the present invention relates to installations for manufacturing pulp and relates more particularly to such installations using as bleaching agent hydrogen peroxide produced by an installation on the site of the installation for manufacturing pulp paper.
  • Installations for the production of oxygen peroxide generally use a process comprising the following steps: a) reduction in a hydrogenator of an organic solution of an anthraquinone derivative, with hydrogen, in the presence of a catalyst; b) oxidation after filtration of the catalyst, of the reduced solution with a gas or a mixture of gases containing oxygen; c) treatment of the solution with water to extract the hydrogen peroxide formed; d) recycling to the hydrogenator of the organic solution extracted with water, after treatment in whole or in part, with a basic aqueous solution.
  • the invention aims to remedy the drawbacks caused by the discharge of effluents from an installation for producing hydrogen peroxide.
  • the invention also relates to an installation for manufacturing paper pulp, in particular chemical pulp intended for the implementation of the process defined above and comprising at least one station for impregnating the material resulting from grinding. wood, a cooking station, and a station for bleaching paper pulp, these stations being each supplied by a source of basic treatment solution, characterized in that the source of basic solution is the outlet of the effluent from the basic treatment of the working solution of a hydrogen peroxide production installation on the site of the pulp manufacturing installation.
  • the single figure is a schematic view of an installation for producing hydrogen peroxide associated with an installation for manufacturing paper pulp on a common site according to the invention.
  • Installation shown in the figure includes installed on the same site, an installation I for the production of hydrogen peroxide and an installation II for the production of paper pulp.
  • Installation I for the production of hydrogen peroxide comprises three main devices in the form of columns: a catalytic hydrogenator 1, a counter-current oxidizer 2, and a water extractor 3. It also includes numerous associated equipment.
  • a booster-condenser assembly 4 for recirculating the gaseous mixture containing hydrogen, associated with the ydrogé ⁇ nator, a filter 6, a pump 7, a heat exchanger 8, a water cooler 9, an overhead condenser 10 and an air compressor 11 associated with the oxidizer, a pipe 12, as short as possible, connecting the base of the oxidizer 2 to that of the extractor 3 and a coalescer 14 and a pump 15 for recycling the working solution.
  • FIG. 1 also shows a line 16 for supplying the hydrogenator with make-up hydrogen, a line 17 for supplying air to the compressor 11, a line 18 for supplying the ex ⁇ tractor 3 in demineralized water, a pipe 19 for the production of hydrogen peroxide, which leaves from the base of the extractor 3 and ends at the installation II for the production of paper pulp consuming hydrogen peroxide at the same concentration , and a pipe 21 for recycling the working solution.
  • Installation II is located on the same site as installation I for the production of hydrogen peroxide.
  • the installation for producing hydrogen peroxide further comprises a device 22 for treating a fraction of the working solution with a basic solution, placed on a branch 23 of the recycling loop for the working solution, for example immediately downstream of coalescer 14.
  • the treatment device 22 is intended to remove from the portion derived from the working solution of the compounds coming from degradation, essentially by oxidation, solvents and anthraquinone derivatives to maintain the acidity of the working solution at an appropriate level.
  • the treatment device 22 is supplied with a sodium hydroxide solution which, after treatment of the portion derived from the working solution, leaves the installation via a pipe 24 for supplying the installation with basic solution.
  • a sodium hydroxide solution which, after treatment of the portion derived from the working solution, leaves the installation via a pipe 24 for supplying the installation with basic solution.
  • II for the production of paper pulp is a Kraft type chemical pulp installation.
  • a station 25 for impregnating the products resulting from slicing or sawing or crushing wood includes among others, a station 25 for impregnating the products resulting from slicing or sawing or crushing wood, a cooking station 26, a delignification station 27 and a station for bleaching the pulp to which it is connected.
  • the treatment stations 25 are each supplied by a source of basic treatment solution.
  • the source of basic solution for the treatment stations 25 to 28 of the installation II for manufacturing paper pulp is constituted by the outlet of the device 22 for treatment with basic solution of the solution of work of the installation I of peroxide production.
  • This output is constituted by the line 24 connected to the stations 25 to 28 by branches 29.30, - 31.32 respectively.
  • bleach station 28 In the bleaching station 28, several successive bleaching processes use the action of sodium hydroxide on the paper pulp in known manner. However, bleach station 28 has been shown in the drawing as comprising only one line 31 for supplying basic solution.
  • the working solution consisting of at least one anthraquinone derivative and at least one organic solvent
  • the recycling line 21 connected to the discharge of the pump 15, and a stream of hydrogen-containing gas is also introduced at the base of the hydrogenator.
  • This gas stream consists on the one hand of the gas stream drawn off at the top of the hydrogenator, recirculated by the booster-condenser assembly 4, and on the other hand, of additional hydrogen arriving via line 16.
  • the anthraquinone derivative constituting the working solution is preferably chosen from the 2 alkyl 9.10 anthraquinones in which the alkyl substituent comprises from 1 to 5 carbon atoms, such as the ethyl, ethyl, sec-butyl, tert-butyl radicals , tertio-a yl, iso-amyl, as well as the corresponding tetrahydro-5,6,7,8 derivatives, or among the dialkyl 9,10 anthra ⁇ quinones in which the alkyl substituents, identical or different, comprise from 1 with 5 carbon atoms, such as methyl, ethyl, tert-butyl radicals, for example 1.3 dimethyl, 1.4 dimethyl, 2.3 dimethyl, 2.7 dimethyl, 1.3 diethyl, 2.7 ditertio-butyl, 2 ethyl 6 tert-butyl and the corresponding tetrahydro-5,6,7,8 derivative
  • the organic solvent constituting the working solution is preferably a mixture of a non-polar compound and a polar compound.
  • the non-polar compound is preferably chosen from petroleum fractions with a boiling point above 140 ° C. containing predominantly aromatic hydrocarbons containing at least 9 carbon atoms, such as the isomers of trimethylbenzene, the isomers of tetramethylbenzene , tert-butylbenzene, isomers of methylnaphthalene, isomers of diethylnaphthalene.
  • the polar compound is preferably chosen from saturated alcohols preferably containing from 7 to 11 carbon atoms, such as diisobutylcarbinol, trimethyl-3,5,5 hexanol, isoheptanol, acid esters carboxylic acids such as cyclohexyl methyl acetate sold under the name of "Sextate", heptyl acetate, butyl benzoate, ethyl heptanoate, esters of phosphoric acid such as tributyl phosphate , tri (2 ethyl butyl) phosphate, tri phosphate (2 ethyl hexyl), tri (n-octyl) phosphate, tetrasubstituted ureas such as tetra (n-butyl urea).
  • saturated alcohols preferably containing from 7 to 11 carbon atoms, such as diisobutylcarbinol, trimethyl-3,5,5 hexanol
  • the working solution is thus partially reduced.
  • the reduced solution drawn off from the base of the hydrogenator by the pump 7 via the filter 6, therefore contains hydroquinone derivatives (for example 80% tetrahydroanthrahydroquinone and 20% anthrahydroquinone).
  • the quantity of hydrogen peroxide expressed in grams, that a liter of working solution is capable of supplying at the end of the oxidation step if the rendering of this step in 1Oxider 2 is 100% , is designated by "hydrogen peroxide equivalent”.
  • This potential mass concentration of peroxide corresponds to a molar concentration which is equal to the molar concentration of all the reoxidizable anthrahydroquinone forms in the working solution.
  • the hydrogenation is carried out at a temperature between 50 and 70 ° C., with a pressure in the gaseous sky of the hydrogenator (pressure which regulates the flow of hydrogen) from 0.8 to 1.5 approximately bar, and the hydrogen peroxide equivalent is adjusted to a value between approximately 7 and 9 g / l, by adjusting the residence time in the hydrogenator, for a given concentration of anthraquinone forms.
  • the reduced working solution withdrawn from the hydrogenator is filtered at 6 to remove all traces of catalyst, then cooled at 8 and then at 9 to a temperature of the order of 35 to 40 °.
  • the pressure of the gaseous overhead of the oxidizer is maintained at a value between 2 and 4 bars.
  • the reduced working solution is thus oxidized in 2, the head fluid of the oxidizer being partially condensed in 10.
  • the hydrogen peroxide formed by the oxidation reaction is withdrawn from the base of the oxidizer, in an amount equal to the product of the hydrogen peroxide equivalent mentioned above by the yield of the oxidizer, mixed with the working solution. oxidized again.
  • This liquid is sent directly via line 12, thanks to the difference in driving pressure, to the base of the extractor 3, which operates a little above atmospheric pressure.
  • the extractor is carried out a liquid-liquid extraction by means of demineralized water introduced at the top of the extractor.
  • a water-hydrogen peroxide solution is drawn from the base of the latter, the hydrogen peroxide concentration is adjusted to the value necessary for its direct use in installation II for making paper pulp.
  • the hydrogen peroxide concentration is chosen to be less than 15% by weight, for example between 5 to 12% by weight.
  • the working solution separated from the hydrogen peroxide is drawn off from the top of the extractor 3, freed from the droplets of aqueous phase which it has entrained in the coalescer 14, then sent by the pump 15 to the heat exchanger 8, in which it heats up, and from there is recycled to the base of the hydrogenator 1.
  • the degraded compounds contained in the working solution circulating in the recycling line which are essentially formed by oxidation of solvents and anthraquinone derivatives must be eliminated from the working solution because they increase the acidity of the organic phase and modify the surface tension of the liquid, which is likely to create problems on the stage of extraction, and reduce both the activity and the selectivity of the hydrogenation catalyst.
  • a fraction of the working solution is therefore derived from the main stream at the outlet of the coalescer 14 and treated using the sodium hydroxide solution in the treatment device 22, to maintain the acidity of the working solution below of a reasonable level.
  • the basic solution from the treatment device 22 is sent via line 24 to the installation II for manufacturing paper pulp and distributed in the branches 29 to 32 to be introduced into successive stations 25 to 28, for impregnation , cooking, delignification and blanching.
  • the soda solution from the hydrogen peroxide production installation is used in the form of a mixture of soda and sodium sulfide received by a pipe 34.
  • the abovementioned basic treatment effluent is used at the delignification station 27 as a source of alkali using oxygen received via a pipe 35.
  • the basic treatment effluent is used as an alkali source, in a step "E” of alkaline extraction or in a step “Eo” of alkaline extraction reinforced with oxygen from paper pulp.
  • the effluent of the basic treatment of the working solution of the hydrogen peroxide production installation is mixed with part of the aqueous hydrogen peroxide solution.
  • a hydrogen peroxide stabilizer is added to the basic solution of hydrogen peroxide.
  • This stabilizing agent is chosen from carboxylic, aminomethylenecarboxylic, phosphonic and aminomethylenephosphonic compounds.
  • this stabilizing agent is chosen from ethylenediamine tetraacetic acid (“EDTA”) or its salts, diethylenetriaminepentaacetic acid (“DTPA”) or its salts, polyacrylic acids, ethylenediaminetetramethylenephosphonic acid or its salts, diethylenetriaminepentamethylenephosphonic acid or its salts, 1,2-diamino acid NNN'N 'tetramethylenephosphonic acid or its salts, hydroxyethylbismethylenephosphonic acid or its salts.
  • EDTA ethylenediamine tetraacetic acid
  • DTPA diethylenetriaminepentaacetic acid
  • polyacrylic acids ethylenediaminetetramethylenephosphonic acid or its salts
  • diethylenetriaminepentamethylenephosphonic acid or its salts 1,2-diamino acid NNN'N 'tetramethylenephosphonic acid or its salts
  • the basic solution of hydrogen peroxide can also be used in a reinforced alkaline extraction stage with oxygen and with hydrogen peroxide "Eop".
  • the basic solution of hydrogen peroxide can also be used in a bleaching stage of the paper pulp, leads to a temperature above 100 ° C. and to a pressure above atmospheric pressure, in the presence of a gas. or a mixture of gases containing oxygen.
  • the basic solution used corresponds to the basic solution for treating the working solution of the installation for the production of hydrogen peroxide. It can be a sodium hydroxide solution at a concentration of between 0.01 and 10 M and preferably between 1 and 3 M.

Abstract

A plant for making paper pulp and particularly chemical pulp, including at least one impregnation station (25) for impregnating a material produced by crushing wood, a cooking station (20), and a paper pulp bleaching station (28), each of said stations being supplied with a basic processing solution from a source. Said basic solution source (24) is the outlet for a basic processing effluent from the working solution of a plant (I) for producing hydrogen peroxide in situ in a paper pulp manufacturing plant (II).

Description

Procède et Installation de fabrication de pâte a papier utilisant les effluents de traitement basiques d'une Installation de production de peroxyde d'hydrogène.Process and installation for the production of pulp using the basic treatment effluents of a hydrogen peroxide production installation.
La présente invention se rapporte aux installa¬ tions de fabrication de pâte à papier et concerne plus particulièrement de telles installations utilisant comme agent de blanchiment du peroxyde d'hydrogène produit par une installation sur le site de l'installation de fabrica¬ tion de pâte à papier.The present invention relates to installations for manufacturing pulp and relates more particularly to such installations using as bleaching agent hydrogen peroxide produced by an installation on the site of the installation for manufacturing pulp paper.
Les installations de production du peroxyde d'oxygène mettent généralement en oeuvre un procédé comprenant les étapes suivantes : a) réduction dans un hydrogénateur d'une solu¬ tion organique d'un dérivé anthraquinonigue, par de l'hydrogène, en présence d'un catalyseur; b) oxydation après filtration du catalyseur, de la solution réduite par un gaz ou un mélange de gaz contenant de l'oxygène; c) traitement de la solution par de l'eau pour extraire le peroxyde d'hydrogène formé; d) recyclage à l'hydrogénateur de la solution organique extraite à l'eau, après traitement en totalité ou partiellement, par une solution aqueuse basique.Installations for the production of oxygen peroxide generally use a process comprising the following steps: a) reduction in a hydrogenator of an organic solution of an anthraquinone derivative, with hydrogen, in the presence of a catalyst; b) oxidation after filtration of the catalyst, of the reduced solution with a gas or a mixture of gases containing oxygen; c) treatment of the solution with water to extract the hydrogen peroxide formed; d) recycling to the hydrogenator of the organic solution extracted with water, after treatment in whole or in part, with a basic aqueous solution.
Dans les installations classiques de production de peroxyde d'hydrogène, la solution basique ayant servi au traitement, conserve une basicité substantielle et doit donc être neutralisée pour pouvoir être rejetée alors qu'elle pourrait encore être utilisée dans une opération industrielle qui serait mise en oeuvre sur le site de l'installation de production du peroxyde d'hydrogène.In conventional hydrogen peroxide production installations, the basic solution used for the treatment retains a substantial basicity and must therefore be neutralized in order to be able to be rejected while it could still be used in an industrial operation which would be implemented. at the site of the hydrogen peroxide production facility.
En outre, le traitement de neutralisation qui nécessite des opérations supplémentaires ne permet cepen- dant pas aux effluents d'être dépourvus de tout danger pour l'environnement.Furthermore, the neutralization treatment which requires additional operations does not, however, allow the effluents to be free from any danger to the environment.
Dans une usine de fabrication de papier, on utilise des solutions basiques en de nombreux points du processus de traitement de la pâte à papier. L'invention vise donc à remédier aux inconvé¬ nients causés par le rejet des effluents d'une installa¬ tion de production d'eau oxygénée.In a paper manufacturing plant, basic solutions are used at many points in the pulp processing process. The invention therefore aims to remedy the drawbacks caused by the discharge of effluents from an installation for producing hydrogen peroxide.
Elle a donc pour objet un procédé de fabrication de pâte à papier, comprenant des phases de traitement à l'aide d'une solution basique, caractérisé en ce que la solution basique est constituée par l'effluent du traite¬ ment basique de la solution de travail utilisée dans un procédé de production de peroxyde d'hydrogène mis en oeuvre sur le site de la fabrication de la pâte à papier.It therefore relates to a process for manufacturing paper pulp, comprising treatment phases using a basic solution, characterized in that the basic solution consists of the effluent from the basic treatment of the solution. of work used in a process for the production of hydrogen peroxide implemented on the site of the manufacture of paper pulp.
L'invention a également pour objet une installa¬ tion de fabrication de pâte à papier notamment de pâte chimique destinée à la mise en oeuvre du procédé défini ci-dessus et comprenant au moins une station d'imprégna- tion de la matière résultant du broyage du bois, une station de cuisson, et une station de blanchiment de la pâte à papier, ces stations étant alimentées chacune par une source de solution basique de traitement, caractérisée en ce que la source de solution basique est la sortie de l'effluent du traitement basique de la solution de travail d'une installation de production de peroxyde d'hydrogène sur le site de l'installation de fabrication de pâte à papier.The invention also relates to an installation for manufacturing paper pulp, in particular chemical pulp intended for the implementation of the process defined above and comprising at least one station for impregnating the material resulting from grinding. wood, a cooking station, and a station for bleaching paper pulp, these stations being each supplied by a source of basic treatment solution, characterized in that the source of basic solution is the outlet of the effluent from the basic treatment of the working solution of a hydrogen peroxide production installation on the site of the pulp manufacturing installation.
L'invention sera mieux comprise à la lecture de la description qui va suivre, donnée uniquement à titre d'exemple et faite en se référant au dessin annexé, sur lequel :The invention will be better understood on reading the description which follows, given solely by way of example and made with reference to the appended drawing, in which:
La figure unique est une vue schématique d'une installation de production de peroxyde d'hydrogène asso- ciée à une installation de fabrication de pâte à papier sur un site commun suivant l'invention.The single figure is a schematic view of an installation for producing hydrogen peroxide associated with an installation for manufacturing paper pulp on a common site according to the invention.
L'installation représentée sur la figure com¬ prend installées sur le même site, une installation I de production de peroxyde d'hydrogène et une installation II de production de pâte à papier. L'installation I de production de peroxyde de l'hydrogène comprend trois appareils principaux en forme de colonnes : un hydrogénateur catalytique 1, un oxydeur à contre-courant 2, et un extracteur à eau 3. Elle com- porte également de nombreux équipements associés à ces trois appareils, dont seuls certains ont été représentés: un ensemble surpresseur-condenseur 4 de recirculation du mélange gazeux contenant l'hydrogène, associé à l' ydrogé¬ nateur, un filtre 6, une pompe 7, un échangeur de chaleur 8, un réfrigérant à eau 9, un condenseur de tête 10 et un compresseur d'air 11 associés à l'oxydeur, une conduite 12, aussi courte que possible, reliant la base de l'oxy¬ deur 2 à celle de l'extracteur 3 et un coalesceur 14 et une pompe 15 pour le recyclage de la solution de travail. On a également représenté sur la figure 1, une conduite 16 d'alimentation de l'hydrogénateur en hydrogène d'appoint, une conduite 17 d'alimentation en air du compresseur 11, une conduite 18 d'alimentation de l'ex¬ tracteur 3 en eau déminéralisée, une conduite 19 de production de peroxyde d'hydrogène, qui part de la base de l'extracteur 3 et aboutit à l'installation II de produc¬ tion de pâte à papier consommant du peroxyde d'hydrogène sous la même concentration, et une conduite 21 de recy¬ clage de la solution de travail. L'installation II se trouve sur le même site que l'installation I de production de peroxyde d'hydrogène.The installation shown in the figure includes installed on the same site, an installation I for the production of hydrogen peroxide and an installation II for the production of paper pulp. Installation I for the production of hydrogen peroxide comprises three main devices in the form of columns: a catalytic hydrogenator 1, a counter-current oxidizer 2, and a water extractor 3. It also includes numerous associated equipment. to these three devices, only some of which have been shown: a booster-condenser assembly 4 for recirculating the gaseous mixture containing hydrogen, associated with the ydrogé¬ nator, a filter 6, a pump 7, a heat exchanger 8, a water cooler 9, an overhead condenser 10 and an air compressor 11 associated with the oxidizer, a pipe 12, as short as possible, connecting the base of the oxidizer 2 to that of the extractor 3 and a coalescer 14 and a pump 15 for recycling the working solution. FIG. 1 also shows a line 16 for supplying the hydrogenator with make-up hydrogen, a line 17 for supplying air to the compressor 11, a line 18 for supplying the ex¬ tractor 3 in demineralized water, a pipe 19 for the production of hydrogen peroxide, which leaves from the base of the extractor 3 and ends at the installation II for the production of paper pulp consuming hydrogen peroxide at the same concentration , and a pipe 21 for recycling the working solution. Installation II is located on the same site as installation I for the production of hydrogen peroxide.
L'installation de production de peroxyde d'hy¬ drogène comprend en outre un dispositif 22 de traitement par une solution basique d'une fraction de la solution de travail, placé sur une dérivation 23 de la boucle de recyclage de la solution de travail, par exemple immédia¬ tement en aval du coalesceur 14.The installation for producing hydrogen peroxide further comprises a device 22 for treating a fraction of the working solution with a basic solution, placed on a branch 23 of the recycling loop for the working solution, for example immediately downstream of coalescer 14.
Le dispositif de traitement 22 est destiné à éliminer de la portion dérivée de la solution de travail des composés provenant de la dégradation, essentiellement par oxydation, des solvants et des dérivés anthraquinoni- ques pour maintenir l'acidité de la solution de travail à un niveau approprié.The treatment device 22 is intended to remove from the portion derived from the working solution of the compounds coming from degradation, essentially by oxidation, solvents and anthraquinone derivatives to maintain the acidity of the working solution at an appropriate level.
Dans le présent exemple, le dispositif de traitement 22 est alimenté par une solution de soude qui après traitement de la portion dérivée de la solution de travail sort de l'installation par une conduite 24 d'ali¬ mentation en solution basique de l'installation II de fabrication de pâte à papier. L'installation II représentée très schématique- ment est une installation de fabrication de pâte à papier chimique de type Kraft.In the present example, the treatment device 22 is supplied with a sodium hydroxide solution which, after treatment of the portion derived from the working solution, leaves the installation via a pipe 24 for supplying the installation with basic solution. II for the production of paper pulp. Installation II very schematically shown is a Kraft type chemical pulp installation.
Elle comporte entre autres, une station 25 d'imprégnation des produits résultant du tranchage ou du sciage ou du broyage du bois, une station 26 de cuisson, une station 27 de délignification et une station de blanchiment de la pâte à papier à laquelle est reliée la conduite 19 d'alimentation en peroxyde d'hydrogène prove¬ nant de l'installation I. Ainsi qu'il est bien connu dans la technique, les stations de traitement 25 sont alimentées chacune par une source de solution basique de traitement.It includes among others, a station 25 for impregnating the products resulting from slicing or sawing or crushing wood, a cooking station 26, a delignification station 27 and a station for bleaching the pulp to which it is connected. the pipe 19 for supplying hydrogen peroxide from the installation I. As is well known in the art, the treatment stations 25 are each supplied by a source of basic treatment solution.
Suivant l'invention, la source de solution basique pour les stations de traitement 25 à 28 de l'ins- tallation II de fabrication de pâte à papier est consti¬ tuée par la sortie du dispositif 22 de traitement par solution basique de la solution de travail de l'installa¬ tion I de production de peroxyde.According to the invention, the source of basic solution for the treatment stations 25 to 28 of the installation II for manufacturing paper pulp is constituted by the outlet of the device 22 for treatment with basic solution of the solution of work of the installation I of peroxide production.
Cette sortie est constituée par la conduite 24 reliée aux stations 25 à 28 par des embranchements 29,30,- 31,32 respectivement.This output is constituted by the line 24 connected to the stations 25 to 28 by branches 29.30, - 31.32 respectively.
Dans la station de blanchiment 28, plusieurs processus de blanchiment successifs mettent en oeuvre de manière connue l'action de la soude sur la pâte à papier. Cependant, la station de blanchiment 28 a été représentée au dessin comme ne comportant qu'une seule conduite 31 d'alimentation en solution basique.In the bleaching station 28, several successive bleaching processes use the action of sodium hydroxide on the paper pulp in known manner. However, bleach station 28 has been shown in the drawing as comprising only one line 31 for supplying basic solution.
En fonctionnement, la solution de travail, constituée d'au moins un dérivé anthraquinonique et d'au moins un solvant organique, est introduite à la base de l'hydrogénateur 1 via la conduite de recyclage 21 reliée au refoulement de la pompe 15, et un courant de gaz contenant de l'hydrogène est également introduit à la base de l'hydrogénateur. Ce courant gazeux est constitué d'une part du courant gazeux soutiré au sommet de l'hydrogéna¬ teur, recirculé par l'ensemble surpresseur-condensateur 4, et d'autre part, d'hydrogène d'appoint arrivant via la conduite 16.In operation, the working solution, consisting of at least one anthraquinone derivative and at least one organic solvent, is introduced at the base of the hydrogenator 1 via the recycling line 21 connected to the discharge of the pump 15, and a stream of hydrogen-containing gas is also introduced at the base of the hydrogenator. This gas stream consists on the one hand of the gas stream drawn off at the top of the hydrogenator, recirculated by the booster-condenser assembly 4, and on the other hand, of additional hydrogen arriving via line 16.
Le dérivé anthraquinonique constitutif de la solution de travail est choisi de préférence parmi les 2 alkyl 9,10 anthraquinones dans lesquelles le substituant alkyle comprend de 1 à 5 atomes de carbone, tel que les radicaux éthyle, éthyle, sec-butyle, tertio-butyle, tertio-a yle, iso-amyle, ainsi que les dérivés tétrahydro- 5,6,7,8 correspondants, ou parmi les dialkyl 9,10 anthra¬ quinones dans lesquelles les substituants alkyles, identi¬ ques ou différents, comprennent de 1 à 5 atomes de carbo¬ ne, tel que les radicaux méthyle, éthyle, tertio-butyle, par exemple 1,3 diméthyle, 1,4 diméthyle, 2,3 diméthyle, 2,7 diméthyle, 1,3 diéthyle, 2,7 ditertio-butyle, 2 éthyle 6 tertio-butyle et les dérivés tétrahydro-5,6,7,8 corres¬ pondants. Le solvant organique constitutif de la solution de travail est de préférence un mélange d'un composé non polaire et d'un composé polaire. Le composé non polaire est choisi de préférence parmi les coupes pétrolières à point d'ébullition supérieur à 140°C contenant majoritai¬ rement des hydrocarbures aromatiques comportant au moins 9 atomes de carbone, tel que les isomères du triméthylben- zene, les isomères du tétraméthylbenzène, le tertio- butylbenzène, les isomères du méthylnaphtalène, les isomères du di éthylnaphtalène. Le composé polaire est choisi de préférence parmi les alcools saturés comportant de préférence de 7 à 11 atomes de carbone, tels que le diiso-butylcarbinol, le triméthyl-3, 5, 5 hexanol, l'iso- heptanol, les esters d'acides carboxyliques tels que l'acétate de méthyle cyclohexyl commercialisé sous le nom de "Sextate", l'acétate d'heptyle, le benzoate de butyle, l'heptanoate d'éthyle, les esters de l'acide phosphorique tels que le phosphate de tributyle, le phosphate de tri (2 éthyl butyle), le phosphate de tri (2 éthyl hexyle), le phosphate de tri (n-octyle), les urées tétrasubstituées telles que la tétra (n-butyl urée).The anthraquinone derivative constituting the working solution is preferably chosen from the 2 alkyl 9.10 anthraquinones in which the alkyl substituent comprises from 1 to 5 carbon atoms, such as the ethyl, ethyl, sec-butyl, tert-butyl radicals , tertio-a yl, iso-amyl, as well as the corresponding tetrahydro-5,6,7,8 derivatives, or among the dialkyl 9,10 anthra¬ quinones in which the alkyl substituents, identical or different, comprise from 1 with 5 carbon atoms, such as methyl, ethyl, tert-butyl radicals, for example 1.3 dimethyl, 1.4 dimethyl, 2.3 dimethyl, 2.7 dimethyl, 1.3 diethyl, 2.7 ditertio-butyl, 2 ethyl 6 tert-butyl and the corresponding tetrahydro-5,6,7,8 derivatives. The organic solvent constituting the working solution is preferably a mixture of a non-polar compound and a polar compound. The non-polar compound is preferably chosen from petroleum fractions with a boiling point above 140 ° C. containing predominantly aromatic hydrocarbons containing at least 9 carbon atoms, such as the isomers of trimethylbenzene, the isomers of tetramethylbenzene , tert-butylbenzene, isomers of methylnaphthalene, isomers of diethylnaphthalene. The polar compound is preferably chosen from saturated alcohols preferably containing from 7 to 11 carbon atoms, such as diisobutylcarbinol, trimethyl-3,5,5 hexanol, isoheptanol, acid esters carboxylic acids such as cyclohexyl methyl acetate sold under the name of "Sextate", heptyl acetate, butyl benzoate, ethyl heptanoate, esters of phosphoric acid such as tributyl phosphate , tri (2 ethyl butyl) phosphate, tri phosphate (2 ethyl hexyl), tri (n-octyl) phosphate, tetrasubstituted ureas such as tetra (n-butyl urea).
La solution de travail est ainsi partiellement réduite. La solution réduite, soutirée de la base de l'hydrogénateur par la pompe 7 via le filtre 6, contient donc des dérivés hydroquinoniques (par exemple 80% de tétrahydroanthrahydroquinone et 20% d'anthrahydroquinone). La quantité de peroxyde d'hydrogène, exprimée en gramme, qu'un litre de solution de travail est susceptible de fournir à l'issue de l'étape d'oxydation si le rende¬ ment de cette étape dans 1Oxydeur 2 est de 100%, est désignée par "équivalent peroxyde d'hydrogène". Cette concentration massique potentielle en peroxyde correspond à une concentration molaire qui est égale à la concentra- tion molaire de l'ensemble des formes anthrahydroquinoni- ques réoxydables dans la solution de travail.The working solution is thus partially reduced. The reduced solution, drawn off from the base of the hydrogenator by the pump 7 via the filter 6, therefore contains hydroquinone derivatives (for example 80% tetrahydroanthrahydroquinone and 20% anthrahydroquinone). The quantity of hydrogen peroxide, expressed in grams, that a liter of working solution is capable of supplying at the end of the oxidation step if the rendering of this step in 1Oxider 2 is 100% , is designated by "hydrogen peroxide equivalent". This potential mass concentration of peroxide corresponds to a molar concentration which is equal to the molar concentration of all the reoxidizable anthrahydroquinone forms in the working solution.
Dans le cas présent, on effectue l'hydrogénation à une température comprise entre 50 et 70°C, avec une pression dans le ciel gazeux de l'hydrogénateur (pression qui régule le débit d'hydrogène) de 0,8 à 1,5 bar environ, et on règle l'équivalent peroxyde d'hydrogène à une valeur comprise entre 7 et 9 g/1 environ, par ajustement du temps de séjour dans l'hydrogénateur, pour une concentration donnée en formes anthraquinoniques. La solution de travail réduite soutirée de 1 ' ydrogénateur est filtrée en 6 pour éliminer toute trace de catalyseur, puis refroidie en 8 puis en 9 jusqu'à une température de l'ordre de 35 à 40°. La pression du ciel gazeux de 1Oxydeur est maintenue à une valeur comprise entre 2 et 4 bars. La solution de travail réduite est ainsi oxydée en 2, le fluide de tête de 1Oxydeur étant partiellement condensé en 10.In the present case, the hydrogenation is carried out at a temperature between 50 and 70 ° C., with a pressure in the gaseous sky of the hydrogenator (pressure which regulates the flow of hydrogen) from 0.8 to 1.5 approximately bar, and the hydrogen peroxide equivalent is adjusted to a value between approximately 7 and 9 g / l, by adjusting the residence time in the hydrogenator, for a given concentration of anthraquinone forms. The reduced working solution withdrawn from the hydrogenator is filtered at 6 to remove all traces of catalyst, then cooled at 8 and then at 9 to a temperature of the order of 35 to 40 °. The pressure of the gaseous overhead of the oxidizer is maintained at a value between 2 and 4 bars. The reduced working solution is thus oxidized in 2, the head fluid of the oxidizer being partially condensed in 10.
Le peroxyde d'hydrogène formé par la réaction d'oxydation est soutiré de la base de 1Oxydeur, dans une quantité égale au produit de l'équivalent peroxyde d'hy¬ drogène précité par le rendement de 1Oxydeur, en mélange avec la solution de travail de nouveau oxydée. Ce liquide est envoyé directement via la conduite 12, grâce à la différence de pression motrice, à la base de l'extracteur 3, lequel fonctionne un peu au-dessus de la pression atmosphérique. Dans l'extracteur s'effectue une extraction liquide-liquide au moyen de l'eau déminéralisée introduite au sommet de l'extracteur. On soutire de la base de ce dernier une solution eau-peroxyde d'hydrogène, dont la concentration en pe¬ roxyde d'hydrogène est réglée sur la valeur nécessaire pour son utilisation directe dans l'installation II de fabrication de pâte à papier. La concentration en peroxyde d'hydrogène est choisie inférieure à 15% en poids, par exemple comprise entre 5 à 12% en poids.The hydrogen peroxide formed by the oxidation reaction is withdrawn from the base of the oxidizer, in an amount equal to the product of the hydrogen peroxide equivalent mentioned above by the yield of the oxidizer, mixed with the working solution. oxidized again. This liquid is sent directly via line 12, thanks to the difference in driving pressure, to the base of the extractor 3, which operates a little above atmospheric pressure. In the extractor is carried out a liquid-liquid extraction by means of demineralized water introduced at the top of the extractor. A water-hydrogen peroxide solution is drawn from the base of the latter, the hydrogen peroxide concentration is adjusted to the value necessary for its direct use in installation II for making paper pulp. The hydrogen peroxide concentration is chosen to be less than 15% by weight, for example between 5 to 12% by weight.
La solution de travail séparée du peroxyde d'hydrogène est soutirée du sommet de l'extracteur 3, débarrassée des gouttelettes de phase aqueuse qu'elle a entraînées dans le coalesceur 14, puis envoyée par la pompe 15 à l'échangeur de chaleur 8, dans lequel elle se réchauffe, et, de là, recyclée à la base de l'hydrogéna¬ teur 1.The working solution separated from the hydrogen peroxide is drawn off from the top of the extractor 3, freed from the droplets of aqueous phase which it has entrained in the coalescer 14, then sent by the pump 15 to the heat exchanger 8, in which it heats up, and from there is recycled to the base of the hydrogenator 1.
Les composés dégradés contenus dans la solution de travail circulant dans la conduite de recyclage qui sont essentiellement formés par oxydation des solvants et des dérivés anthraquinoniques doivent être éliminés de la solution de travail car ils accroissent l'acidité de la phase organique et modifient la tension superficielle du liquide, ce qui risque de créer des problèmes à l'étage d'extraction, et réduisent à la fois l'activité et la sélectivité du catalyseur d'hydrogénation.The degraded compounds contained in the working solution circulating in the recycling line which are essentially formed by oxidation of solvents and anthraquinone derivatives must be eliminated from the working solution because they increase the acidity of the organic phase and modify the surface tension of the liquid, which is likely to create problems on the stage of extraction, and reduce both the activity and the selectivity of the hydrogenation catalyst.
Une fraction de la solution de travail est donc dérivée du courant principal à la sortie du coalesceur 14 et traitée à l'aide de la solution de soude dans le dispositif de traitement 22, pour maintenir l'acidité de la solution de travail au-dessous d'un niveau raisonnable.A fraction of the working solution is therefore derived from the main stream at the outlet of the coalescer 14 and treated using the sodium hydroxide solution in the treatment device 22, to maintain the acidity of the working solution below of a reasonable level.
Ensuite, la phase organique est lavée avec une solution aqueuse d'acide minéral, puis soigneusement par de l'eau dans des équipements non représentés avant d'être recyclée.Then, the organic phase is washed with an aqueous solution of mineral acid, then carefully with water in equipment not shown before being recycled.
La solution basique issue du dispositif de traitement 22 est envoyée par la conduite 24 à l'installa¬ tion II de fabrication de pâte à papier et répartie dans les embranchements 29 à 32 pour être introduite dans les stations successives 25 à 28, d'imprégnation, de cuisson, de délignification et de blanchiment.The basic solution from the treatment device 22 is sent via line 24 to the installation II for manufacturing paper pulp and distributed in the branches 29 to 32 to be introduced into successive stations 25 to 28, for impregnation , cooking, delignification and blanching.
Dans l'opération de cuisson de la pâte à papier réalisée à la station de cuisson 26, la solution de soude issue de l'installation de production de peroxyde d'hydro¬ gène est utilisée sous forme de mélange de soude et de sulfure de sodium reçu par une conduite 34.In the paper pulp cooking operation carried out at cooking station 26, the soda solution from the hydrogen peroxide production installation is used in the form of a mixture of soda and sodium sulfide received by a pipe 34.
Dans l'étape de délignification, l'effluent de traitement basique précité est utilisé à la station de délignification 27 comme source d'alcali mettant en oeuvre de l'oxygène reçu par une conduite 35.In the delignification step, the abovementioned basic treatment effluent is used at the delignification station 27 as a source of alkali using oxygen received via a pipe 35.
Dans la station de blanchiment, l'effluent de traitement basique est utilisé comme source d'alcali, dans une étape "E" d'extraction alcaline ou dans une étape "Eo" d'extraction alcaline renforcée à l'oxygène de pâte à papier.In the bleaching station, the basic treatment effluent is used as an alkali source, in a step "E" of alkaline extraction or in a step "Eo" of alkaline extraction reinforced with oxygen from paper pulp.
Toujours dans la station de blanchiment, l'ef¬ fluent du traitement basique de la solution de travail de l'installation de production de peroxyde d'hydrogène est mélangé avec une partie de la solution aqueuse de peroxyde 'hydrogène.Still in the bleaching station, the effluent of the basic treatment of the working solution of the hydrogen peroxide production installation is mixed with part of the aqueous hydrogen peroxide solution.
Un agent stabilisant du peroxyde d'hydrogène est ajouté à la solution basique de peroxyde d'hydrogène. Cet agent stabilisant est choisi parmi les composés carboxyliques, aminométhylènecarboxyliques, phosphoniques, aminométhylènephosphoniques.A hydrogen peroxide stabilizer is added to the basic solution of hydrogen peroxide. This stabilizing agent is chosen from carboxylic, aminomethylenecarboxylic, phosphonic and aminomethylenephosphonic compounds.
En particulier, cet agent stabilisant est choisi parmi l'acide l'éthylènediamine tétraacétique ( "EDTA" ) ou ses sels, l'acide diéthylènetriaminepentaacétique ( "DTPA" ) ou ses sels, les acides polyacryliques, l'acide éthylène- diaminetetraméthylènephosphonique ou ses sels, l'acide diéthylènetriaminepentaméthylènephosphonique ou ses sels, l'acide diamino-1,2 NNN'N' tétraméthylènephosphonique ou ses sels, l'acide hydroxyéthylbisméthylènephosphonique ou ses sels.In particular, this stabilizing agent is chosen from ethylenediamine tetraacetic acid ("EDTA") or its salts, diethylenetriaminepentaacetic acid ("DTPA") or its salts, polyacrylic acids, ethylenediaminetetramethylenephosphonic acid or its salts, diethylenetriaminepentamethylenephosphonic acid or its salts, 1,2-diamino acid NNN'N 'tetramethylenephosphonic acid or its salts, hydroxyethylbismethylenephosphonic acid or its salts.
La solution basique de peroxyde d'hydrogène peut être de plus utilisée dans un stade d'extraction alcaline renforcée à l'oxygène et au peroxyde d'hydrogène "Eop". La solution basique de peroxyde d'hydrogène peut être également utilisée dans un stade de blanchiment de la pâte à papier, conduit à une température supérieure à 100°C et à une pression supérieure à la pression atmos¬ phérique, en présence d'un gaz ou d'un mélange de gaz contenant de l'oxygène.The basic solution of hydrogen peroxide can also be used in a reinforced alkaline extraction stage with oxygen and with hydrogen peroxide "Eop". The basic solution of hydrogen peroxide can also be used in a bleaching stage of the paper pulp, leads to a temperature above 100 ° C. and to a pressure above atmospheric pressure, in the presence of a gas. or a mixture of gases containing oxygen.
La solution basique utilisée correspond à la solution basique de traitement de la solution de travail de l'installation de production de peroxyde d'hydrogène. Elle peut être une solution d'hydroxyde de sodium à une concentration comprise entre 0,01 et 10 M et de préférence entre 1 et 3 M.The basic solution used corresponds to the basic solution for treating the working solution of the installation for the production of hydrogen peroxide. It can be a sodium hydroxide solution at a concentration of between 0.01 and 10 M and preferably between 1 and 3 M.
Il conviendrait également de mentionner que la solution basique n'est pas nécessairement l'unique source d'alcali mais peut intervenir en complément d'une autre source d'alcali.It should also be mentioned that the basic solution is not necessarily the only source of alkali but can be used in addition to another source of alkali.
Grâce à l'agencement qui vient d'être décrit, on tire profit dans l'installation de fabrication de pâte à papier de la source de solution basique que constituent les effluents basiques de l'installation de production de peroxyde d'hydrogène se trouvant sur le site de l'instal¬ lation de fabrication de pâte à papier alors que dans une installation de production de peroxyde d'hydrogène indé- pendante, ces effluents basiques ne trouvaient pas d'uti¬ lisation et devaient donc être rejetés. Thanks to the arrangement which has just been described, advantage is taken in the pulp production installation of the basic solution source that constitutes the basic effluents of the installation for producing hydrogen peroxide located on the site of the pulp manufacturing facility, while in an independent hydrogen peroxide production facility, these basic effluents could not be used and should therefore be rejected.

Claims

REVENDICATIONS
1. Procédé de fabrication de pâte à papier, comprenant des phases de traitement à l'aide d'une solu¬ tion basique, caractérisé en ce que la solution basique est constituée par l'effluent du traitement basique de la solution de travail utilisée dans un procédé de production de peroxyde d'hydrogène mis en oeuvre sur le site de la fabrication de la pâte à papier.1. A method of manufacturing paper pulp, comprising treatment phases using a basic solution, characterized in that the basic solution consists of the basic treatment effluent of the working solution used in a process for the production of hydrogen peroxide implemented on the site of the manufacture of paper pulp.
2. Procédé suivant la revendication 1, compre- nant une phase de cuisson de pâte chimique de type Kraft, caractérisé en ce que la solution basique résiduelle du traitement de la solution de travail utilisée dans le procédé de production de peroxyde d'hydrogène est une solution de soude qui est mélangée avec du sulfure de sodium.2. Method according to claim 1, comprising a phase of cooking Kraft type chemical pulp, characterized in that the residual basic solution from the treatment of the working solution used in the process for producing hydrogen peroxide is a soda solution which is mixed with sodium sulfide.
3. Procédé suivant l'une des revendications 1 et3. Method according to one of claims 1 and
2, comprenant une étape de délignification mettant en oeuvre de 1 'oxygène et dans laquelle l'effluent du traite¬ ment basique est utilisé comme source d'alcali. 2, comprising a delignification step using oxygen and in which the basic treatment effluent is used as a source of alkali.
4. Procédé suivant l'une des revendications 1 à4. Method according to one of claims 1 to
3, comprenant une phase de blanchiment de la pâte à papier dans laquelle l'effluent du traitement basique est utilisé dans une étape d'extraction alcaline "E" ou une étape d'extraction alcaline renforcée d'oxygène "Eo" de la pâte à papier.3, comprising a bleaching phase of the paper pulp in which the effluent from the basic treatment is used in an alkaline extraction step "E" or an oxygen-reinforced alkaline extraction step "Eo" from the pulp paper.
5. Procédé suivant la revendication 4, dans lequel l'effluent du traitement basique est mélangé avec une partie de la solution aqueuse de peroxyde d'hydrogène produite sur le site de la fabrication de la pâte à papier.5. The method of claim 4, wherein the effluent from the basic treatment is mixed with part of the aqueous solution of hydrogen peroxide produced at the site of the manufacture of the pulp.
6. Procédé suivant la revendication 5, dans lequel un agent stabilisant du peroxyde d'hydrogène est ajouté à la solution basique de peroxyde d'hydrogène.6. The method of claim 5, wherein a stabilizing agent of hydrogen peroxide is added to the basic solution of hydrogen peroxide.
7. Procédé suivant la revendication 6, dans lequel l'agent stabilisant du peroxyde d'hydrogène est choisi parmi les composés carboxyliques, aminométhylène- carboxyliques, phosphoniques, aminométhylènephosphoniques.7. The method of claim 6, wherein the hydrogen peroxide stabilizing agent is chosen from carboxylic, aminomethylene-carboxylic, phosphonic, aminomethylene-phosphonic compounds.
8. Procédé suivant la revendication 7, dans lequel l'agent stabilisant du peroxyde d'hydrogène est choisi parmi l'acide l'éthylenediamine tétraacétique ( "EDTA" ) ou ses sels, l'acide diéthylènetriaminepentaacé- tique ( "DTPA" ) ou ses sels, les acides polyacryliques, l'acide éthylènediaminetetraméthylènephosphonique ou ses sels, l'acidediéthylènetriaminepentaméthylènephosphonique ou ses sels, l'acide diamino-1,2 NNN'N' tétraméthylène- phosphonique ou ses sels, l'acide hydroxyéthylbisméthylè- nephosphonique ou ses sels.8. The method of claim 7, wherein the stabilizing agent of hydrogen peroxide is selected from ethylenediamine tetraacetic acid ("EDTA") or its salts, diethylenetriaminepentaacetic acid ("DTPA") or its salts, polyacrylic acids, ethylenediaminetetramethylenephosphonic acid or its salts, acidediethylenetriaminepentamethylenephosphonic acid or its salts, diamino-1,2 NNN'N 'tetramethylene-phosphonic acid or its salts, hydroxyethylbismethylenophosphonic acid or its salts .
9. Procédé selon l'une des revendications 5 à 8, dans lequel la solution basique de peroxyde d'hydrogène est utilisée dans un stade d'extraction alcaline renforcée à l'oxygène et au peroxyde d'hydrogène "Eop".9. Method according to one of claims 5 to 8, in which the basic solution of hydrogen peroxide is used in an alkaline extraction stage reinforced with oxygen and with hydrogen peroxide "Eop".
10. Procédé suivant l'une des revendications 4 à 9, dans lequel le stade de blanchiment de la pâte est conduit à une température supérieur à 100°C et à une pression supérieure à la pression atmosphérique, en présence d'un gaz ou d'un mélange de gaz contenant de 1'oxygène.10. Method according to one of claims 4 to 9, wherein the pulp bleaching stage is carried out at a temperature above 100 ° C and at a pressure above atmospheric pressure, in the presence of a gas or d 'a mixture of gases containing oxygen.
11. Procédé selon l'une des revendications 1 et 3 à 10, dans lequel la base utilisée dans la solution basique de traitement de la solution de travail du procédé de production du peroxyde d'hydrogène est l'hydroxyde de sodium.11. Method according to one of claims 1 and 3 to 10, wherein the base used in the basic solution for treating the working solution of the process for producing hydrogen peroxide is sodium hydroxide.
12. Procédé selon la revendication 11, dans lequel la concentration de l'hydroxyde de sodium est comprise entre 0,01 et 10 M et de préférence entre 1 et 3 M.12. The method of claim 11, wherein the concentration of sodium hydroxide is between 0.01 and 10 M and preferably between 1 and 3 M.
13. Installation de fabrication de pâte à papier notamment de pâte chimique destinée à la mise en oeuvre du procédé suivant l'une quelconque des revendications 1 à 12 et comprenant au moins une station (25) d'imprégnation de la matière résultant du broyage du bois, une station (26) de cuisson, et une station (28) de blanchiment de la pâte à papier, ces stations étant alimentées chacune par une source de solution basique de traitement, caractérisée en ce que la source de solution basique est la sortie (24) de l'effluent du traitement basique de la solution de travail d'une installation (I) production de peroxyde d'hydrogène sur le site de l'ins¬ tallation (II) de fabrication de pâte à papier.13. Installation for manufacturing paper pulp, in particular chemical pulp intended for the implementation of the method according to any one of claims 1 to 12 and t comprenan AT LEAST s station (25) impregnation of the material resulting from the grinding timber, a station (26) for cooking, and a station (28) for paper pulp bleaching, these stations being each fed by a source of basic treatment solution, characterized in that the source of basic solution is the outlet (24) of the effluent from the basic treatment of the working solution of an installation (I) production of hydrogen peroxide on the site of the plant (II) for manufacturing paper pulp.
14. Installation suivant la revendication 13, comprenant en outre une station de délignification (27) et dans laquelle la source de solution basique (24) est reliée à la station de délignification (27) à laquelle est également reliée une source d'oxygène. 14. Installation according to claim 13, further comprising a delignification station (27) and in which the source of basic solution (24) is connected to the delignification station (27) to which is also connected an oxygen source.
PCT/FR1996/000302 1995-02-28 1996-02-27 Method and apparatus for making paper pulp using basic processing effluents from a hydrogen peroxide production plant WO1996027046A1 (en)

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FR95/02315 1995-02-28

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Publication number Priority date Publication date Assignee Title
EP2006441A1 (en) * 2007-06-18 2008-12-24 Andritz, Inc. Processes and systems for the bleaching of lignocellulosic pulps following cooking with soda and anthraquinone
AU2008202566B2 (en) * 2007-06-18 2011-11-03 Andritz Inc. Processes and Systems for the Bleaching of Lignocellulosic Pulps Following Cooking with Soda and Anthraquinone
US8262856B2 (en) 2007-06-18 2012-09-11 Andritz Inc. Processes and systems for the bleaching of lignocellulosic pulps following cooking with soda and anthraquinone

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FR2731021A1 (en) 1996-08-30

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