WO1993015264A1 - Delignification en phase gazeuse de matieres lignocellulosiques - Google Patents

Delignification en phase gazeuse de matieres lignocellulosiques Download PDF

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Publication number
WO1993015264A1
WO1993015264A1 PCT/US1993/000408 US9300408W WO9315264A1 WO 1993015264 A1 WO1993015264 A1 WO 1993015264A1 US 9300408 W US9300408 W US 9300408W WO 9315264 A1 WO9315264 A1 WO 9315264A1
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WO
WIPO (PCT)
Prior art keywords
chlorine dioxide
pulp
ozone
lignocellulosic material
delignification
Prior art date
Application number
PCT/US1993/000408
Other languages
English (en)
Inventor
Sudhir K. Mendiratta
David W. Cawlfield
Glenn F. Rudie
Venketa R. Parthasarathy
Original Assignee
Olin Corporation
Mead Corporation
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 Olin Corporation, Mead Corporation filed Critical Olin Corporation
Priority to BR9305760A priority Critical patent/BR9305760A/pt
Priority to JP5513284A priority patent/JPH07502082A/ja
Priority to AU34769/93A priority patent/AU656658B2/en
Priority to EP93903543A priority patent/EP0705361A1/fr
Publication of WO1993015264A1 publication Critical patent/WO1993015264A1/fr
Priority to FI943466A priority patent/FI943466A0/fi

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Classifications

    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
    • D21C9/10—Bleaching ; Apparatus therefor
    • D21C9/147—Bleaching ; Apparatus therefor with oxygen or its allotropic modifications
    • D21C9/153—Bleaching ; Apparatus therefor with oxygen or its allotropic modifications with ozone
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
    • D21C9/10—Bleaching ; Apparatus therefor
    • D21C9/12—Bleaching ; Apparatus therefor with halogens or halogen-containing compounds
    • D21C9/14—Bleaching ; Apparatus therefor with halogens or halogen-containing compounds with ClO2 or chlorites
    • D21C9/144—Bleaching ; Apparatus therefor with halogens or halogen-containing compounds with ClO2 or chlorites with ClO2/Cl2 and other bleaching agents in a multistage process

Definitions

  • the present invention relates to a process for sequential or simultaneous gas phase delignification of lignocellulosic material for use in paper making which produces delignified cellulosic material having reduced absorbed organic halides (AOX) .
  • AOX organic halides
  • Chlorine-based chemicals such as chlorine, chlorine dioxide and hypochlorite have been used in pulp bleaching for several decades and continue to be used for removing lignin and bleaching the pulp to high brightness.
  • the extent of delignification and bleaching (the degree of brightness obtained) is determined by the type of pulp being delignified and bleached and the proposed end use of the paper.
  • chlorine-based delignifying and bleaching agents have been employed in the prior art, there are produced chlorinated organics. These compounds are toxic and are present in the discharge effluents from one or more of the stages of the paper making process (eg. bleaching stage). A relatively smaller percentage of such chlorinated organics remain in the pulp and eventually appear in the paper product.
  • Hydrogen peroxide is widely used to reinforce the alkaline extraction stages which are carried out after the chlorination and chlorine dioxide stages, but so far neither oxygen nor a combination of oxygen and hydrogen peroxide could match the efficiency of chlorination.
  • Ozone because of its high oxidation potential should offer a better alternative, but its uses are limited because it must be used in the gaseous state and ozone generators produce only low concentrations of ozone in oxygen or air.
  • Ozone has been used alone as a single stage bleaching agent, or in a multi-stage bleaching process which may include treatment with other bleaching agents such as oxygen, peroxides, chlorine dioxide and hypochlorite.
  • the fundamental bleaching variables affecting the use of ozone include (a) the type of pulp (hardwood or softwood), (b) the pulping process used to produce the pulp, (c) pre-treatment of the pulp prior to ozonization, (d) sequential treatment of ozone and other bleaching chemicals, (e) pulp consistency, (f) ozone concentration and charge, (g) temperature, (h) time, and (i) pH.
  • ozone as a strong oxidant, tended to attack and degrade cellulose as is the case with oxygen. In the later instance, the degradation of cellulose is minimized by using a magnesium salt as a protector.
  • Another option to reduce the discharge of chlorinated organic compounds is to reduce the chlorine usage in the first stage of the bleaching process.
  • Two alternatives that produce no significant degradation of pu p properties have been commercialized for this purpose. These are (a) extended delignification in the cooking stage and (b) oxygen delignification. These alternatives, with proper extraction, reduce the chlorinated organic compounds in the bleached pulp and ensuing effluent to sufficiently low levels.
  • a third option to reduce the generation of chlorinated organics in a bleaching process is to substitute chlorine dioxide for chlorine.
  • Chlorine dioxide is a relatively strong oxidant compared to chlorine. To achieve the same degree of delignification, it requires only about thirty-eight weight percent chlorine dioxide on the pulp compared with one hundred weight percent of chlorine.
  • these processes are of the DEDED type wherein the chlorine dioxide stage (D) is followed by the conventional extraction (E) and additional chlorine dioxide (D) stages.
  • the pulp and discharge effluents resulting from the processes of this option contain higher concentrations of chlorinated organics than are acceptable and/or desirable. Processes using both oxygen delignification and chlorine dioxide substitution have been suggested, but do not achieve the desired and/or regulated concentrations of chlorine containing residues in either the pulp or the effluent.
  • Chlorine dioxide and ozone have found wide uses as disinfectants in water treatment/purification applications, delignifying and/or as a bleaching agent in pulp and paper production, and in a number of other uses because of their high oxidizing power .
  • Ozone is used as a delignifying chemical to remove or reduce the lignin from the lignocellulosic material, but because of its high oxidizing power, it is indiscriminatory in its tendency to attack both lignin an cellulose thereby producing inferior pulp.
  • Chlorine dioxide in solution has been used to brighten and produce a clean pulp in paper manufacture.
  • the use of liquid chlorine dioxide in the first stage of a multiple stage bleaching process is not as effective as is using chlorine as a delignifying agent.
  • the use of elemental chlorine has the undesirable effect of producing organo-chlorine compounds, which are measurable as adsorbable organic halides (AOX) , in the effluent steams of processing facilities.
  • AOX adsorbable organic halides
  • chlorate salt a chloride ion source or reducing agent
  • chlorate ion reacts to produce a mixture of chlorine and chlorine dioxide.
  • the chlorine present in these processes is an undesired by-product which adds to the AOX concentrations in discharge flow streams.
  • Many processes have been developed to produce chlorine dioxide with lower chlorine concentrations by adding a reducing agent.
  • Some reducing agents which have been used in these applications include methanol or other organic compounds, sulfur, sulfur dioxide or other sulfur-oxygen species having a sulfur valence of less than +6, and carbon monoxide. When organic compounds are used, unreacted volatile organics, including organic acids, are present in the product gas.
  • the sulfate or sulfuric acid produced accumulates as a waste product.
  • gaseous reducing agents such as sulfur dioxide or carbon monoxide
  • reactor designs and process control systems must protect against unreacted reducing agent leaving the system with the chlorine dioxide gas.
  • Chlorine dioxide has been produced in prior art processes from chlorate salts by the addition of an excess of the acid used. While this acid is slowly neutralized by the accumulation of alkali metal ions that enter the process with the chlorate salt, the accumulation of salts must be removed as a waste stream. This waste stream is either liquid or solid in every process currently practiced commercially.
  • Chloric acid is, however, not commercially available, although its preparation has been taught in U.S. Patent 3,810,969 issued May 14, 1974 to A.A. Schlumberger. Schlumberger teaches a process for producing chloric acid by passing an aqueous solution containing from 0.2 gram mole to 11 gram moles per liter of an alkali metal chlorate such as sodium chlorate through a selected cationic exchange resin at a temperature from 5° to 40° C. The process produces an aqueous solution containing from 0.2 gram mole to about 4.0 gram moles of HC10_ per liter.
  • K.L. Hardee et al in U.S. Patent No. 4,798,715 issued Jan. 17,1989, describe a process to produce chlorine dioxide by electrolyzing a chloric acid solution produced by passing an aqueous solution of an alkali metal chlorate through an ion exchange resin.
  • the electrolysis is carried out using an electrocatalytic cathode where the catalyst is, for example, one or more valve metal oxides which may be combined with a platinum group metal oxide, or a platinum group metal, or oxides of a platinum group metal, magnetite, ferrite, or mixed metal oxides.
  • the electrolyzed solution contains a mixture of chlorine dioxide and chloric acid, which is fed to an extractor in which the chlorine dioxide is stripped off.
  • the ion exchange resin is regenerated with hydrochloric acid and an acidic solution of an alkali metal chloride formed.
  • Such processes require the regeneration of the ion exchange resin with acid to remove the alkali metal ions and the use or treatment and disposal of the acidic salt solution.
  • concentration of chloric acid that can be produced by an ion exchange process is limited since more concentrated chloric acid solutions attack the ion exchange resins used in the process.
  • the production of chloric acid by means of a cation exchange resin is not economically attractive.
  • ozone generators produce ozone by a continuous high voltage electric discharge in presence of an oxygen containing feed gas.
  • the ozone generator contains a stainless steel tube and a shell heat exchanger.
  • High voltage alternating current is imposed on a high voltage electrode consisting of a permanent stainless steel tube on one side of a dielectric material.
  • the dielectric glass tube centered in the stainless steel tube which has a ground electrode allows the electric discharge to occur as corona discharge across the.discharge gap between the dielectric and the ground electrode.
  • As the oxygen containing feed gas flows through the "corona" a portion of the oxygen is converted to ozone. Since much of the electrical energy supplied to form ozone is lost as heat, an efficient method of heat removal is incorporated into the design of the generator.
  • Gas phase bleaching with chlorine or chlorine dioxide has been proposed over the years in various patents and publications as a method of reducing the bleaching time while cutting chemical costs.
  • Gas phase bleaching is carried out on higher consistency pulp using mixtures of chlorine dioxide and steam and/or inert gases such as air or nitrogen.
  • U.S. Patent No. 3,725,193, issued April 3, 1973 to R.M. DeMontigny et al. describes a process for bleaching high consistency pulps, which includes preheating the pulp by direct steaming. A gaseous mixture of chlorine dioxide diluted with steam or a non-reactive gas is then passed through the pulp. The contact period is in the order of a fraction of a second. The bleached pulp was then held in a retention vessel for 30 minutes. Unreacted chlorine dioxide was removed from a bleaching tower by aeration. The final pH of the bleached pulp was 5.2. Ozone treatment of pulp is practiced under three pulp consistencies. They are ultra low consistency treatment, medium consistency treatment and high consistency treatment.
  • High consistency treatment of pulp involves the use of gaseous ozone applications.
  • Advantages alleged for gas phase bleaching of high consistency wood pulps include superior control of bleaching because of the short retention times employed; reduced chemical usage for the same brightness; and low water usage and effluent volume.
  • the gas phase bleaching of pulp is well documented, but no information is available on the use of gaseous chlorine dioxide and ozone either sequentially or simultaneously for the delignification of pulps. Both chlorine dioxide and ozone are strong oxidizing agents, but their ability to complement one another in the delignification process has been not explored.
  • Canadian patents number 2,032,315; 2,031,848; and 2,031,850 teach the sequential addition of aqueous chlorine dioxide and ozone at points separated from one another and each being at at least one place in the line and this stage being free from intermediate washing between places for addition.
  • Heterogenous sequential treatment of pulp with aqueous solutions of ozone and chlorine dioxide require repeated filtering and thickening of pulp stock to adjust for the various consistency requirements of each treatment step.
  • Another object of the present invention is to mix the chlorine dioxide gas from the state of the art generation processes with an ozone oxygen gas mixture to get a highly reactive chlorine dioxide and ozone gas mixture.
  • any residual elemental chlorine formed in the chlorine dioxide generation is oxidized by mixing and reacting it with ozone, thereby eliminating the chances of chlorine to react with pulp to generate AOX.
  • Another object of the present invention is that any residual elemental chlorine formed in the reaction between chlorine dioxide and lignocellulosic material is destroyed by the reaction of lignocellulosic material with ozone, thereby reducing the chances for the formation of absorbable organic halides (AOX) .
  • AOX absorbable organic halides
  • Another object of the present invention is that gaseous chlorine dioxide added to the lignocellulosic material acts as an acidic pH buffer of pH 2 - 5, the pH range conducive for ozone delignification.
  • Yet another object of the invention is that chlorine dioxide addition to the pulp inhibits the carbohydrate degradation reactions of ozone which are responsible for the strength loss of the pulp.
  • lt is still another advantage of the present invention that a clean pulp material is obtained in less time and at lower cost in needed equipment when compared with conventional processes.
  • an improved process for delignifying lignocellulosic material which comprises treating the lignocellulosic material sequentially or simultaneously with gaseous chlorine dioxide and ozone and then transporting it into a reaction chamber where it is retained for a short period of time to complete the reaction and delignification of the lignocellulosic material. Then an alkaline extraction is performed. The delignified material is then separated from the effluent. This effluent contains less than about 1.0 kg absorbable organic halides (AOX) per ton of lignocellulosic material.
  • AOX absorbable organic halides
  • Suitable pulps which can be bleached include any of those which are commonly used such as chemical kraft, sulfite or mechanical and recycle pulps. Pulp having any suitable consistencies may be delignified including those of about 15 percent or higher, for example, from about 25 to about 60 percent can be treated by the process of the present invention. The pulps are preferably shredded or fluffed.
  • Chlorine dioxide gas used as a reactant in the process of the present invention preferably contains low concentrations of elemental chlorine and preferably small amounts of inert gases, such as nitrogen or air.
  • Suitable chlorine dioxide gas used in delignification of pulp is a mixture of chlorine dioxide, gaseous oxygen, and water vapor. Partial pressure of chlorine dioxide in the gas stream is between 10 to 100 mm of Hg.
  • the chlorine dioxide gas has a low elemental chlorine content of less than about 18 percent.
  • the chlorine dioxide gas can also be substantially free of chlorine, preferably less than about 2 percent by weight, and more preferably less than about 1.5 percent by weight based on the weight of chlorine dioxide in the gas.
  • the gaseous mixture contains varying concentrations of oxygen and water vapor.
  • the amount of oxygen can be independently varied to provide molar ratios of 0 uncomfortable to CIO- by volume of from about 1:4 to about 50:1.
  • Water vapor or steam is preferably the primary diluent in the gaseous mixture and replaces other inert gases which are normally used. As a diluent, steam supplies heat to the pulp and minimizes cooling by evaporation which occurs when, for example, air is used as the diluent.
  • Gaseous mixtures containing chlorine dioxide suitable for use in the novel process of the present invention preferably can be produced from concentrated solutions of chloric acid.
  • Conversion of the chloric acid to chlorine dioxide can be accomplished, for example, by cathodic reduction in an electrolytic cell or by contacting the chloric acid with a suitable catalyst in the presence of heat.
  • highly acidic aqueous solutions containing chlorate ions, including chloric acid, perchlorate ions and hydrogen ions are reacted to produce a gaseous mixture of chlorine dioxide, oxygen and water vapor (steam) .
  • the gaseous mixture has low concentrations of inert gases, such as air or nitrogen, and yet provides reduced risks to spontaneous explosions or "puffs".
  • the aqueous solutions have an acid concentration of at least 2 molar, preferably at least 3 molar, and a concentration of chlorate ions of at least 0.02 molar and preferably from about 0.1 to about 3 molar.
  • These acidic solutions preferably are substantially free of ionic impurities such as chloride ions, alkali metal and alkaline earth metal ions.
  • the hydrogen ion concentration from acid in the aqueous solutions may be provided by non-oxidizable inorganic acids such as sulfuric acid, phosphoric acid, chloric acid or perchloric acid.
  • non-oxidizable inorganic acids such as sulfuric acid, phosphoric acid, chloric acid or perchloric acid.
  • the acidic solutions are reacted in the presence of a catalyst which promotes oxygen evolution.
  • Suitable as oxygen-evolving catalysts are, for example, metals and oxides of the elements of Group VIIIA of the Periodic Table of Elements.
  • metals such as the platinum group metals including platinum, palladium, iridium, rhodium or ruthenium; and mixtures or alloys of these platinum group metals may be employed.
  • oxides of platinum group metals such as iridium, rhodium or ruthenium, as well as mixtures of these oxides with platinum group metals or alloys of these precious metals could be suitably employed.
  • iron alloys such as stainless steel, nickel or nickel based alloys, and cobalt based alloys can be used as oxygen-evolving catalysts in the process of the invention.
  • oxygen-evolving catalysts include semiconductive ceramics known as perovskites.
  • perovskites To suppress or minimize the auto-oxidation of chloric acid to perchloric acid, for example where an oxygen-evolving catalyst is employed, it is preferred to use, as the source of chlorate ions, a mixture of chloric acid and a non-oxidizable inorganic acid in which the concentration of chloric acid is low, for example, less than about 20 percent by weight of the aqueous solution providing chlorate ions.
  • These processes for generating chlorine dioxide can be started up in a few minutes and similarly stopped in a short time so that storage of C10_ gas or dissolution in water or a solvent is not required.
  • High purity concentrated chloric acid solutions are produced by the oxidation of high purity hypochlorous acid solutions.
  • One process suitable for producing the chloric acid solutions heats a hypochlorous acid solution, containing from about 35 to about 60 percent by weight of HOC1, at a temperature in the range of from about 25 to about 120° C.
  • Another process for producing the high purity chloric acid solution utilizes anodic oxidation of the high purity concentrated hypochlorous acid solution in an electrolytic cell having an anode compartment, a cathode compartment, and a cation exchange membrane separating the anode compartment from the cathode compartment.
  • this process includes feeding an aqueous solution of hypochlorous acid to the anode compartment, and electrolyzing the aqueous solution of hypochlorous solution at a temperature of from about 0° to about 40°C. to produce the chloric acid solution.
  • Chloric acid solutions can be produced by these processes in any concentrations desired up to about 45% by weight of HC10_ .
  • preferred concentrations are those in the range of from about 30 to about 40% by weight of HC10_ .
  • Generation of the chlorine dioxide gas from the reaction mixture containing chloric acid and the non-oxidizable inorganic acid is preferably conducted at atmospheric pressure in the presence of a diluent gas, such as oxygen, nitrogen or air.
  • a diluent gas such as oxygen, nitrogen or air.
  • the temperature of the reactor mixture should not exceed 120°C, more preferably not more than about 90°C, to avoid decomposition of the chlorine dioxide in the gas phase.
  • pressures can be in the range of from about 15 to about 750, preferably from about 100 to about 500, and more preferably from about 150 to about 300 mm of Hg. At these pressures the temperature of the reaction mixture is in the range of from about 40°C to about 90°C, and preferably from about 50°C to about 80°C.
  • the temperatures and pressures for subatmospheric pressures are selected to maintain continuous boiling of the reaction mixture.
  • the chlorine dioxide gas generator must be in water balance to operate in steady state conditions.
  • the rate of heat addition to the generator determines the quantity of water that is evaporated to maintain steady state concentration, it is necessary to evaporate water continuously at about the same rate at which water is added, with the chloric acid feed solution adjusted for water formed by reaction of the chloric acid.
  • chlorine dioxide gas can be obtained from any commercially available generators directly producing gaseous chlorine, or by removing the gas prior to going to an adsorber for liquifaction, such as those available from Albright and Wilson Americas under the model names R-8, R-9 and R-10, or from other suppliers of similar commercial equipment.
  • Ozone gas can be obtained from any commercially available generators producing ozone by direct electric discharge through air or oxygen.
  • concentration of ozone from the reactor should be not less than 6 percent by weight on the oxygen feed, but not limited to or not exceeding 13 percent by weight of oxygen feed, the point of self detonation of ozone. Preferable concentrations are from about 6 to 8 percent.
  • the ozone gas from the reactor may be taken to a mixing chamber where it may be used to mix the chlorine dioxide gas from the novel generation process described above.
  • Chlorine dioxide can also be obtained from state of the art generators such as the R-8 generator or from other generators supplied by similar commercial equipment vendors.
  • the process of the invention can be practiced using any suitable prior art apparatus such as a conventional bleaching tower.
  • Delignification of pulp may be affected in the initial stages of a multi-stage bleaching process, as well as in any D or DZ stages.
  • the process of the invention requires a rapid mixing and short retention in an apparatus similar to the existing first stage equipment capable of mixing a mixture of gaseous chlorine dioxide and ozone with lignocellulosic material.
  • the delignification of unbleached lignocellulosic material or pulp is accomplished with the use of a gaseous mixture of chlorine dioxide and ozone produced by one of the aforementioned processes and simultaneously charging the gaseous mixture to the pulp or sequentially charging the individual gases to the pulp.
  • the gaseous chlorine dioxide has low concentrations, or is substantially free, of elemental chlorine and is combined with a direct alkaline extraction step in the absence of an intermediate washing to reduce the AOX concentrations in the discharge stream.
  • the delignification of unbleached lignocellulosic material or pulp may be carried out in any suitable equipment in which the unbleached pulp can be contacted with the chlorine dioxide gas.
  • any reactor should be gas tight. Suitable gas tight equipment includes, for example, agitated mixers, static mixers, ribbon blenders, steam chests, high consistency shear mixers, MC pumps, MC mixers, high velocity pipe lines, fluffers, etc.
  • Pressure requirements for the feed of the gaseous mixture of chlorine dioxide and ozone to ensure stability are critical, especially if the gaseous mixture is being introduced into a vacuum chamber.
  • partial pressure of the chlorine dioxide in the chlorine dioxide gas must be limited to about 100 mm of Hg to insure stability. If the chlorine dioxide is
  • the pulp material should be in the range of about 20 to about 50 percent consistency, and more preferably about 30 percent consistency.
  • the pulp material can spend from about 5 seconds to about 45 minutes in the react.on chamber, preferably from about 5 seconds to about 5 minutes, and more preferably from about 5 seconds to about 1 minute contact time in the reaction chamber before exiting.
  • the feed rate of the chlorine dioxide and ozone gas mixture to the lignocellulosic material or pulp can be controlled so that it can be passed through at least one time, and possibly as many as two or three times, such as by the use of pressure differential between the upper inlet side and the lower outlet side before the gas exits through the reaction chamber for reclamation.
  • the lignocellulosic material or pulp can then be passed directly to an alkaline extractor apparatus to undergo the alkaline treatment.
  • an alkaline extraction occur without any intermediate washing in the process of the instant invention, it is possible to use an intermediate wash prior to an alkaline treatment.
  • the elemental chlorine-free C10 2 and ozone mixture is admixed with the pulp in the reactor which is at any suitable pressure including atmospheric, subatmospheric or superatmospheric pressures.
  • the reactor is at subatmospheric pressures which are preferably slightly below those employed in the chlorine dioxide or ozone generator.
  • an eductor which employs ozone and oxygen gas mixture to dilute and to remove chlorine dioxide from the generator and supply it to the pulp reactor.
  • the chlorine dioxide and ozone gas mixture is used in amounts which provide a concentration or ratio of gas mixture to pulp that is suitable for delignifying the unbleached chemical pulp to the desired degree, as indicated, for example, by the selected Kappa number as determined by TAPPI test method T236 cm-85 and accepted by the industry.
  • the delignification of the pulp using the process of the invention is accomplished in surprisingly short contact times, with the delignification rate being independent of pulp temperatures.
  • the temperature of the delignification reaction is not critical and delignification can be carried out at surprisingly low temperatures, from about ambient temperature. Temperatures in the range of from about ambient to about 90°C, preferably ambient to about 80°C, and more preferably, from about 20°C to about 60°C can be employed. At these temperatures minimal time is required.
  • delignification of the pulp normally is carried out under acidic conditions and the acidity can be derived from the chlorine dioxide gas.
  • the pH of the pulp to be treated normally is adjusted so that the final pH of the delignified pulp before extraction is in the range from about 1 to about 6.
  • Residual chlorine dioxide and ozone gas mixture can be suitably removed, such as by passing an inert gas through the pulp and the gaseous mixture can then be passed through a catalytic converter to reclaim oxygen which can be sent to the chlorine dioxide generator or to the ozone generator or to both for further use.
  • An extraction stage (E) is then carried out without an intervening washing step with, for example, caustic soda to solubilize the higher molecular weight oxidized lignins, to hydrolyze organic chlorides to salts, etc.
  • a suitable reducing agent can be added with or prior to adding the extracting agents, such as sodium thiosulfate, sodium hydrosulfite, sodium sulfide, sodium sulfite, hydrogen peroxide, or combinations thereof.
  • the extraction is conducted at temperatures of 60° to about 90°C, and a residence time of about 60 minutes where the final pH is 10.5 or higher.
  • the extraction stage may include the addition of oxygen, a peroxide such as hydrogen peroxide, or hypochlorite, or a combination thereof for enhanced performance.
  • the extracted pulp is filtered and washed to remove water soluble lignins and low molecular weight organic chlorides, among others.
  • the delignified chemical pulp has a Kappa number in the range of from about 1 to about 10, and preferably from about 2 to about 8.
  • the extracted pulp may be subsequently further delignified, for example, using the process of the invention or any known bleaching stage to achieve the final brightness desired.
  • AOX adsorbable organic halides
  • the effluent discharge from the bleaching process of the present invention has less than about 2.0 kg adsorbable organic halides (AOX) per ton of wood pulp.
  • AOX as the term is used herein refers to the sum of the AOX, i.e. adsorbed organic halides, of the several stages of bleaching and alkaline extraction with or without washing.
  • the pulp produced by the present invention has a brightness and viscosity that meet or exceed the requirements of industrial papermaking.
  • a gaseous mixture of chlorine dioxide, oxygen and water vapor is generated by feeding a chloric acid solution containing about 37.16 percent by weight of HC10_ .
  • the generator is maintained at a temperature between about 70° and 73°C by regulating the feed rate of the chloric acid, and by providing sufficient heat of reaction to evaporate the water present in the chloric acid solution and that formed during the generation of chlorine dioxide.
  • the ozone reactor is a commercial reactor using oxygen as the feed gas for ozone generation.
  • the ozone generator is maintained at temperatures between 10°C and 25°c. Two separate gas lines, independently carrying ozone and chlorine dioxide from the respective generators are connected to a small mixing chamber prior to entering the bottom of the reaction vessel.
  • the gaseous mixture is distributed into the pulp through a perforated sparger.
  • the softwood pulp is treated for a time between 1 - 5 minutes with the gaseous mixture.
  • Each delignified pulp sample is equally divided, one half to be washed and the other not washed prior to extraction (E) . Where washing is employed the filtrate and the wash water are collected. Extraction of the delignified pulp is carried out by adding the indicated amount of about 3.5% NaOH by weight on pulp of a 10 percent sodium hydroxide solution. The operating consistency of pulp is about 10 percent. The pulp is held at about 70°C. for about 60 minutes. The extracted pulp is dried, washed and the Kappa Number is determined to be less than 10.
  • the absorbable organic halides (AOX) in the combined solution mixture of the bleach filtrate, wash water, extraction liquor and wash water is determined to be less than 1.0 kg/metric ton of pulp.
  • a continuously stirred hot water jacketed reaction vessel containing a gas distribution device is loaded with 100 gm of oven dried shredded and fluffed softwood pulp having a consistency of about 35 percent.
  • the reaction vessel can act as an equipment vessel for rapid mixing of gas with pulp as well as a retention vessel for the continuation of the delignifying process after mixing the gases with the pulp.
  • the initial Kappa number of the pulp is about 30.0.
  • the initial pulp temperature is at ambient conditions, but warmed up to about 80°C and preferentially maintained between about 40°C and about 60°C.
  • the outlet of the reactor is connected to a series of potassium iodide traps containing 10 percent KI which are acting as gas scrubbers for both the chlorine dioxide and ozone exiting the reaction vessel.
  • the catalytic convertor is employed to remove the organics carried over by the exiting gases and also to remove the moisture from the oxygen which was the carrier gas for both chlorine dioxide and ozone.
  • Two separate gas lines, independently carrying ozone and chlorine dioxide from the respective generators are connected to the bottom of the reaction vessel and distributed into the pulp through a perforated sparger. Each line has a gas metering device to measure accurately the gas flow to the reactor.
  • the chlorine dioxide gas line is also using a spectrophotometric device to measure the concentration of chlorine dioxide flowing to the reactor.
  • the ozone supply line has a concentration measurement and monitoring unit utilizing UV spectrophotometry to measure the concentration of ozone in the carrier gas.
  • a feedback control unit is used to adjust the oxygen feed to the ozone generator.
  • the gases can be fed sequentially either by charging ozone first and then chlorine dioxide and vice versa.
  • the initial pulp pH has a range from 2 to about 8.
  • the pH of the pulp is adjusted by using an acid, preferably sulfuric acid.
  • the pH of the pulp ranges from 2 to 5, but preferably less than 3.
  • the exit gas is taken directly to the KI traps by-passing the catalytic convertor.
  • the chlorine dioxide feed to the pulp is calculated on the basis of the Kappa factor, a measure of chemical charge determined by the Kappa number of the pulp.
  • the Kappa factor is in the range of 0.5 to 2.0.
  • the time for the reaction is varied from one minute to five minutes, but preferably less than about 2 minutes.
  • the ozone charge on the pulp is varied from 0.1 percent to 2.0 percent.
  • the reaction time is varied from one minute to five minutes, but preferably less than about two minutes.
  • the reaction can be carried out in subatmospheric, atmospheric, or superatmospheric pressure.
  • the pressure range is 10 mm of Hg to 760 mm Hg to 1520 mm Hg, preferably between 100 to 1520 mmHg.
  • Each delignified pulp sample is equally divided, one half to be washed and the other not washed prior to 5 extraction (E) . Where washing is employed, the filtrate and the wash water are collected. Extraction of the delignified pulp is carried out by adding the indicated amount of about 3.5 percent sodium hydroxide by weight on pulp of a 10 percent sodium hydroxide solution. The 0 operating consistency of pulp is about 10 percent. The pulp is held at about 70°C for about 60 minutes. The extracted pulp is dried, washed and the Kappa number is determined to be less than 10. The adsorbed organic halides (AOX) in the combined solution mixture of the 5 bleach filtrate, wash water, extraction liquor and wash water is determined to be less than 1.0 kg/metric ton of pulp.
  • AOX adsorbed organic halides
  • the pulp from the extraction step is treated with one or more bleaching sequences involving chlorine o dioxide in aqueous or gaseous form, alkaline extraction with sodium hydroxide reinforced by oxygen and/or hydrogen peroxide and a gaseous mixture of chlorine dioxide and ozone and combinations thereof to obtain pulp of required brightness and strength.
  • the adsorbed 5 organic halides (AOX) in the later bleach plant effluent from the bleaching sequences are found to be less than 0.3. kg/metric ton of pulp.

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Paper (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

Permettant de délignifier des matières lignocellulosiques telles que la pâte de bois, un procédé consiste à traiter ces matières de façon séquentielle ou simultanée avec un gaz, le dioxide de chlore, et de l'ozone, ce qui donne la matière cellulosique délignifiée et des rejets d'effluents dont la teneur en halogénures organiques adsorbés (HOA) est réduite.
PCT/US1993/000408 1992-01-22 1993-01-19 Delignification en phase gazeuse de matieres lignocellulosiques WO1993015264A1 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
BR9305760A BR9305760A (pt) 1992-01-22 1993-01-19 Processo para deslignificaçao de material lignocelulósico
JP5513284A JPH07502082A (ja) 1992-01-22 1993-01-19 リグノセルロール材料の気相脱リグニン化
AU34769/93A AU656658B2 (en) 1992-01-22 1993-01-19 Gas phase delignification of lignocellulosic material
EP93903543A EP0705361A1 (fr) 1992-01-22 1993-01-19 Delignification en phase gazeuse de matieres lignocellulosiques
FI943466A FI943466A0 (fi) 1992-01-22 1994-07-21 Lignoselluloosamateriaalin kaasufaasidelignifiointi

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US82379592A 1992-01-22 1992-01-22
US823,795 1992-01-22

Publications (1)

Publication Number Publication Date
WO1993015264A1 true WO1993015264A1 (fr) 1993-08-05

Family

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Application Number Title Priority Date Filing Date
PCT/US1993/000408 WO1993015264A1 (fr) 1992-01-22 1993-01-19 Delignification en phase gazeuse de matieres lignocellulosiques

Country Status (10)

Country Link
EP (1) EP0705361A1 (fr)
JP (1) JPH07502082A (fr)
AU (1) AU656658B2 (fr)
BR (1) BR9305760A (fr)
CA (1) CA2128408A1 (fr)
FI (1) FI943466A0 (fr)
NZ (1) NZ245712A (fr)
RU (1) RU94036007A (fr)
WO (1) WO1993015264A1 (fr)
ZA (1) ZA93224B (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2743094A1 (fr) * 1995-12-27 1997-07-04 Centre Tech Ind Papier Procede de blanchiment des pates a papier chimiques
WO2002016691A1 (fr) * 2000-08-25 2002-02-28 Akzo Nobel N.V. Procede chimique
US6579412B2 (en) * 1998-05-08 2003-06-17 L'air Liquide - Societe' Anonyme A' Directoire Et Conseil De Surveillance Pour L'etude Et L'exploitation Des Procedes Georges Claude Process for ozone bleaching of low consistency pulp
US6773547B2 (en) * 1998-05-08 2004-08-10 American Air Liquide, Inc. Process for the bleaching of low consistency pulp using high partial pressure ozone
US8524038B2 (en) 2006-03-31 2013-09-03 Oy Lannen Tutkimus—Western Research Inc. Bleaching process of chemical pulp
CN111315802A (zh) * 2017-11-07 2020-06-19 英格维蒂南卡罗来纳有限责任公司 制备低色木质素的方法

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111253424B (zh) 2014-08-06 2023-06-20 加州理工学院 芳族杂环通过地球丰富的无过渡金属的催化剂的甲硅烷基化

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US1957937A (en) * 1930-10-10 1934-05-08 Int Paper Co Process of bleaching fibrous cellulose material
US3725193A (en) * 1969-11-26 1973-04-03 Pulp Paper Res Inst Process and apparatus for the chemical reaction between a gas and a wood pulp
US3810969A (en) * 1971-06-22 1974-05-14 Hooker Chemical Corp Process for the production of chlorine dioxide
US4902381A (en) * 1988-12-09 1990-02-20 Kamyr, Inc. Method of bleaching pulp with ozone-chlorine mixtures
US4959124A (en) * 1989-05-05 1990-09-25 International Paper Company Method of bleaching kraft pulp in a DZED sequence
US5034095A (en) * 1989-06-01 1991-07-23 Oji Paper Co., Ltd. Apparatus and process for the delignification of cellulose pulp

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US4216054A (en) * 1977-09-26 1980-08-05 Weyerhaeuser Company Low-consistency ozone delignification
DE69128287T2 (de) * 1990-08-14 1998-03-19 Int Paper Co Bleichen von chemischem zellstoff mittels chlor/chlordioxid dann durch ozon

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US1957937A (en) * 1930-10-10 1934-05-08 Int Paper Co Process of bleaching fibrous cellulose material
US3725193A (en) * 1969-11-26 1973-04-03 Pulp Paper Res Inst Process and apparatus for the chemical reaction between a gas and a wood pulp
US3810969A (en) * 1971-06-22 1974-05-14 Hooker Chemical Corp Process for the production of chlorine dioxide
US4902381A (en) * 1988-12-09 1990-02-20 Kamyr, Inc. Method of bleaching pulp with ozone-chlorine mixtures
US4959124A (en) * 1989-05-05 1990-09-25 International Paper Company Method of bleaching kraft pulp in a DZED sequence
US5034095A (en) * 1989-06-01 1991-07-23 Oji Paper Co., Ltd. Apparatus and process for the delignification of cellulose pulp

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See also references of EP0705361A4 *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2743094A1 (fr) * 1995-12-27 1997-07-04 Centre Tech Ind Papier Procede de blanchiment des pates a papier chimiques
US6579412B2 (en) * 1998-05-08 2003-06-17 L'air Liquide - Societe' Anonyme A' Directoire Et Conseil De Surveillance Pour L'etude Et L'exploitation Des Procedes Georges Claude Process for ozone bleaching of low consistency pulp
US6773547B2 (en) * 1998-05-08 2004-08-10 American Air Liquide, Inc. Process for the bleaching of low consistency pulp using high partial pressure ozone
US6793771B2 (en) * 1998-05-08 2004-09-21 American Air Liquide, Inc. Ozone bleaching of low consistency pulp
WO2002016691A1 (fr) * 2000-08-25 2002-02-28 Akzo Nobel N.V. Procede chimique
US8524038B2 (en) 2006-03-31 2013-09-03 Oy Lannen Tutkimus—Western Research Inc. Bleaching process of chemical pulp
CN111315802A (zh) * 2017-11-07 2020-06-19 英格维蒂南卡罗来纳有限责任公司 制备低色木质素的方法

Also Published As

Publication number Publication date
RU94036007A (ru) 1996-06-10
CA2128408A1 (fr) 1993-08-05
FI943466A (fi) 1994-07-21
NZ245712A (en) 1994-09-27
BR9305760A (pt) 1997-01-28
AU3476993A (en) 1993-09-01
FI943466A0 (fi) 1994-07-21
EP0705361A1 (fr) 1996-04-10
AU656658B2 (en) 1995-02-09
JPH07502082A (ja) 1995-03-02
ZA93224B (en) 1993-08-18
EP0705361A4 (fr) 1995-09-27

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