EP0517689B1 - A method of producing kraft pulp - Google Patents

A method of producing kraft pulp Download PDF

Info

Publication number
EP0517689B1
EP0517689B1 EP92890125A EP92890125A EP0517689B1 EP 0517689 B1 EP0517689 B1 EP 0517689B1 EP 92890125 A EP92890125 A EP 92890125A EP 92890125 A EP92890125 A EP 92890125A EP 0517689 B1 EP0517689 B1 EP 0517689B1
Authority
EP
European Patent Office
Prior art keywords
white liquor
liquor
cooking
pulp
supply
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP92890125A
Other languages
German (de)
French (fr)
Other versions
EP0517689A1 (en
Inventor
Jian E.C/O Kamyr Inc. Jiang
Joe R. C/O Kamyr Inc Phillips
Brian F. c/o Kamyr Inc. Greenwood
Robert J. C/O Kamyr Inc. Prough
Kaj c/o Kamyr Inc. Henricson
Bertil C. C/O Kamyr Inc. Stromberg
Rolf Ryham
James W. Smith
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ahlstrom Machinery Inc
Original Assignee
Ahlstrom Machinery Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GB919111256A external-priority patent/GB9111256D0/en
Application filed by Ahlstrom Machinery Inc filed Critical Ahlstrom Machinery Inc
Publication of EP0517689A1 publication Critical patent/EP0517689A1/en
Application granted granted Critical
Publication of EP0517689B1 publication Critical patent/EP0517689B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

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
    • D21C11/00Regeneration of pulp liquors or effluent waste waters
    • D21C11/0064Aspects concerning the production and the treatment of green and white liquors, e.g. causticizing green liquor
    • 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
    • D21C3/00Pulping cellulose-containing materials
    • D21C3/02Pulping cellulose-containing materials with inorganic bases or alkaline reacting compounds, e.g. sulfate processes
    • D21C3/022Pulping cellulose-containing materials with inorganic bases or alkaline reacting compounds, e.g. sulfate processes in presence of S-containing compounds
    • 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
    • D21C3/00Pulping cellulose-containing materials
    • D21C3/22Other features of pulping processes
    • D21C3/26Multistage processes

Definitions

  • the present invention relates to a method of producing kraft pulp by cooking comminuted cellulosic fibrous material with white liquor to produce kraft pulp and black liquor, whereby
  • the higher-sulfidity liquor can be used in the impregnation and the lower-sulfidity liquor introduced later, e.g. in the transfer circulation or in the first pulping circuit. It is well-known, as dislosed in J.P. Casey "Pulp and Paper”; Chemistry and Chemical Technology 3rd ed., vol. I, 1980, John Wiley & Sons, New York, p. 470-476, that sulfur-containing gases are released during the digester relief and blow, from condensate stripping, and from other sources.
  • a method of producing kraft pulp from cellulosic comminuted fibrous material utilizing white liquor is provided.
  • the invention is thereby characterized by the following steps: (c) sulfur from the black liquor is recovered by heating the black liquor to produce sulfur-containing off gases; and (d) the recovered sulfur is added to a stream of white liquor made from the remaining black liquor to increase the sulfur content thereof thereby producing said first supply of white liquor deriving from said remaining black liquor.
  • the off gases are treated to produce primarily methane and hydrogen sulfide.
  • the hydrogen sulfide from the treated off gases is fed to a scrubber in which it is brought into contact with white liquor, thereby producing said first supply of white liquor so that an optimum viscosity/kappa ratio can be achieved.
  • the concepts described above are utilized in a practical manner to provide kraft pulp that has an optimum viscosity/kappa ratio, and/or good strength properties, and with good yield.
  • the invention is applicable to a wide variety of different kraft cooking processes, both batch and continuous.
  • the invention can be utilized in continuous digesters having an impregnation zone, or in cooking systems utilizing a separate impregnation vessel from the continuous digester, or in batch digester.
  • the invention can also be utilized in association with co-current movements of white liquor with the pulp, or countercurrent movements, such as are provided in the commercial digesting process marketed by Kamyr, Inc. of Glens Falls, New York under the trademark "MCC".
  • White liqour is that treatment liquid in a kraft process which contains the active cooking chemicals, sodium hydroxide (NaOH) and sodium sulfide (Na 2 S); or white liquor in an extreme situation may contain substantially only NaOH as active ingredient.
  • the white liquor sulfur content in the cook is maintained in the range of 25-35 % (this overall sulfur content ratio is the amount of sodium sulfide to the sum of sodium sulfide and sodium hydroxide applied to the whole cooking process), and according to standard practice in the art, a sulfur content level below 15 % results in a deterioration in the cooking rate and pulp quality.
  • the present invention it has been found that by making two (or more) supplies or streams of white liquor, with different sulfur contents, and applying them to different portions in the kraft cycle, significantly improved results can be achieved.
  • Practicing the invention it is possible to optimize the viscosity/kappa ratio of the produced pulp for any given level of sulfur content, and/or to optimize pulp strength properties.
  • the increase can be dramatic, easily on the order of 25 % for conventional cooks with multiple white liquor additions (co-current), about the same increase for modified continuous cooking (MMCTM), and 15 % or more for extended modified continuous cooking (EMMCTM). Comparable increases occur for batch treatment too.
  • While the exact source of the sulfur for producing the high sulfur content stream or supply of white liquor according to the invention is not critical as long as the sulfur is recovered according to step (c) of claim 1, one exceptionally good source that allows a practical, industrial scale process to be practiced is that shown in US-A-4,929,307 wherein sulfate black liquor is heated to above the cooking temperature so as to split the macro-molecular lignin fraction, to produce sulfur-containing off gases. Those off gases are favourably reacted to produce primarily methane and hydrogen sulfide, and then brought into contact with sulfur depleted white liquor from the normal chemical manufacturing facility of the pulp mill, to produce an extremely high sulfur content white liquor, the hydrogen sulfide being selectively absorbed into the white liquor. That high sulfur content white liquor may then be acted upon to produce at least some significant portions of polysulfide, and then utilized in early stages of the kraft cook.
  • the cooking liquor utilized above is a kraft cooking liquor. It may contain anthraquinone or its derivatives or equivalents, or the like, and the first liquor may be targeted to an impregnation stage, co-current cook stage, or countercurrent cook stage.
  • FIGURE 1 is a schematic view of exemplary apparatus for practicing an exemplary method according to the present invention.
  • FIGURE 1 illustrates exemplary apparatus for use in kraft pulping process.
  • a digester 12 which preferably is a continuous digester such as that sold by Kamyr, Inc. of Glens Falls, New York, but may be a batch digester -- has a stream of off gases 13, and black liquor (residual white liquor containing the reaction products of lignin solubilization) is withdrawn at an intermediate position as indicated at 14, while the kraft pulp produced is discharged at 15.
  • black liquor in line 14 When the black liquor in line 14 is discharged, it may be passed directly to black liquor evaporators, and preferably it is subjected, somewhere in the evaporator chain, to a heat treatment process at step 17 to produce off gases in line 18.
  • the heat treatment of block 17 is preferably that described in US-A-4,929,307.
  • the black liquor passes to evaporators 19 (evaporator 19' may concentrate the black liquor before heat treatment 17 too), which also produce off gases in line 20, then to a conventional recovery boiler 22, with conventional white liquor manufacture at block 23, to produce white liquor in line 24 having depleted sulfur content.
  • the off gases in 18 which may include only those from the heat treatment 17, or also those from the digester line 13, only and from the black liquor evaporators in line 20, or a combination of any two of them -- are preferably first subjected to a drying or absorption stage (as indicated schematically at 27 in FIGURE 1) in order ro remove a majority of the water vapor.
  • the removal of the water vapor increases the concentration of organic sulfur gases.
  • Step 27 is accomplished by drying the gas stream by any conventional means and/or by absorbing or adsorbing the organic portion of the gas onto a solid, or additionally by absorbing the off gas into one of any non-polar liquids (e.g.kerosene or mineral oil).
  • Treatment may be provided of a liquid mixture, but preferably according to the invention further treatment is of the concentrated gas.
  • the next steps in the treatment of the off gases as illustrated in FIGURE 1 are to add hydrogen, and the pass the gas in the presence of the added hydrogen past a hydrogen desulfurization catalyst.
  • This may be accomplished, for example, in the hydrogen desulfurization (HDS) unit 28, with the hydrogen gas from line 29 added to the unit 28 along with the gas in line 18.
  • the hydrogen gas in line 29 can come from any source (e.g. be purchased, from water electrolysis, etc.).
  • the hydrogen desulfurization catalyst consist essentially of a transition metal-molybdenum alloy, particularly a nickel molybdenum or cobalt molybdenum alloy.
  • the product gas stream in line 30 is further acted upon.
  • the gas stream in line 30 contains primarily methane, and hydrogen sulfide, with hydrogen also present.
  • the hydrogen sulfide is then separated out from the gas in stream 30.
  • the hydrogen sulfide may be separated as a gas and then used in its gaseous form in conventional pulping techniques, it may be fed to a scrubber 32 in which it is brought into contact with a caustic solution, preferably kraft white liquor, which contains sodium hydroxide and most likely at least some sodium sulfide. While in the preferred embodiment illustrated in the drawings white liquor is utilized, under some circumstances green liquor may be advantageously utilized, with white liquor subsequently made from the green liquor.
  • White liquor from line 24 is passed into inlet 33 of scrubber 32, the hydrogen sulfide being absorbed in the white liquor and thereby significantly enhancing its sulfur content.
  • the significantly enhanced sulfur content white liquor then passes through the outlet 34 of the scrubber into line 35, to be used in the pulping process.
  • the white liquor in line 35 passes through a polysulfide treatment stage, as illustrated at 36, and then to the impregnation vessel 37 (if a separate impregnation vessel is used) or the like, to be utilized in the pulping cycle.
  • Elemental sulfur may be added at 36 instead of polysulfide.
  • the gas stream that remains, in line 38, contains primarily methane, but also some hydrogen. Ultimately, the gas in line 38 may become the source of the hydrogen for line 29.
  • the high sulfur content white liquor in line 35 is provided at an early stage of the cook, e.g. at the beginning of the impregnation vessel 37, or impregnation stage if impregnation takes place in the digester 12 itself, or at multiple places in the impregnation zone and/or vessel 37.
  • a countercurrent impregnation flow may be provided, in which case the higher sulfur content liquor is added near the end of the impregnation stage.
  • Part of the sulfide depleted white liquor in line 24 is passed into line 41, and it is then introduced into the cook, preferably at multiple locations, as indicated at 42 and 43 in FIGURE 1.
  • the low sulfur content white liquor in line 41 may vary widely.
  • it may be added to the middle of the impregnation vessel 37, at one, two, or more co-current stages in the digester 12, or at one, two, or more countercurrent stages in the digester 12 (e.g. for modified continuous cooking, or extended modified continuous cooking).
  • the liquor in line 41 may also be utilized in a batch process.
  • While the drawing illustrates only two streams or supplies of white liquor, 35, 41, having different sulfur content, as many different sulfur content streams as desired may be produced.
  • two series connected units 32 may be utilized, the first producing the highest sulfur content level white liquor, while the second produces an intermediate (between lines 35 and 41) sulfur content level white liquor.
  • the intermediate sufidity white liquor is added earlier in the cook than the white liquor in line 41.
  • the relative amount of sulfur content of the white liquor added at various stages within the kraft cycle may also be varied widely according to the invention.
  • the kraft pulping process is to be a multi-level conventional cook, that is white liquor is added at two or more points in the cook and flows co-currently with the pulp, then about 60% of the total cooking chemical is added to the impregnation vessel (e.g. in line 35), while about 25% is added to the first co-current stage (e.g. at 42) and about 15% to the second co-current stage (e.g. at 43).
  • the amount of sulfide provided in line 35 is about 60-90%, and if practical may be almost 100% of the total sulfide in all of the white liquor streams, that is the white liquor in stream 41 is substantially fully sulfide depleted.
  • the stream in line 35 in this embodiment may be generated by passing 35-65% of the total volume of white liquor through the unit 32, the remaining 65-35% of the white liquor being added through line 41.
  • about 35% of the total volume of white liquor is passed through unit 32, and this high sulfur content white liquor is then added to the top circulation in the conventional impregnation vessel 37.
  • the sulfide-depleted white liquor in line 41 is added to middle circulation in the vessel 37 in the amount of about 25-35% of the total cooking chemical from white liquor, while about 20-25% of the total cooking chemical, in the sulfide depleted white liquor in line 41, is added to the continuous digester 12 first cooking circulation.
  • the low sodium sulfide content liquor in line 41 may also be added at 44 to an oxygen delignification or bleaching stage 45 as a source of sodium hydroxide.
  • the viscosity to kappa ratio may be increased by about 0.2-0.3 units if almost all sulfide is added to the impregnation stage (e.g. in line 35 to vessel 37).
  • the total sulfur content is added in the impregnation stage (line 35), the total volume of white liquor added in line 35 being about 40-65% of the total volume of white liquor used in the pulping process.
  • polysulfide is added to the white liquor.
  • this can be done by the MOXY (TM) process in which some of the sodium sulfide in the white liquor is partially oxidized to produce polysulfide, or by other known polysulfide processes.
  • polysulfide from an external source may merely be introduced into the white liquor, e.g. polysulfide produced by reacting elemental sulfur with sulfide ions in an aqueous solution under proper conditions; or elemental sulfur may be added to the white liquor instead of polysulfide.
  • the amount of polysulfide produced, or added, in stage 36 is about 0.5%-8% on wood, expressed as elemental sulfur. Typically, about 2% polysulfide is desirable. If 2% polysulfide is used in conjunction with extended modified continuous cooking, a kraft pulp with a kappa of about 12.5, a viscosity of about 33.7 cp, and a yield of about 44.6% can be made. This yield is equal to that of a conventional cook or extended modified continuous cook pulp at a kappa of about 18-20 without polysulfide, and the viscosity is equivalent to that of a conventional cook pulp at kappa 26, or an extended modified continuous cook pulp at kappa 17.
  • a slurry of wood chips is treated in a plurality of consecutive stages (e.g. impregnation stage, first and second co-current or countercurrent cooking stages) with white liquor using first and second supplies, differing in the sulfur content thereof.
  • the chips are treated with white liquor under cooking conditions (e.g. in digester 12) in at least one stage, to effect kraft cooking thereof.
  • Black liquor is withdrawn (at 14) and sulfur is recovered from the black liquor, as by heating treating it (at 17) according to the process of US-A-4,929,307, evaporating it (in 19), etc. (see 22 and 23 in FIGURE 1).
  • the recovered sulfur is added to the first supply of white liquor, as in unit 32, to significantly increase the sulfur content thereof, so that the sulfur content of the liquor in line 35 is substantially greater than that in line 24 (which is sulfur depleted, and may be near zero).
  • the relative sulfur contents of the white liquors in lines 35 and 24 are controlled so as to optimize the viscosity/kappa ratio and/or physical strength properties.
  • the invention allows advantageous production of kraft pulp to be practiced on an industrial scale -- that is, larger production than reasonably possible in a laboratory, with complete chemical recovery.
  • the invention may be illustrated by various examples.
  • Tables IA-IE provide the results of laboratory batch cooks using split white liquor streams with variable sulfur content, according to the invention, and conventional cooks for comparison purposes.
  • CK means conventional kraft cooking
  • MCK means kraft cooking with multiple introductions of white liquor, with more than one co-current cooking stage
  • MCC refers to Kamyr, Inc.'s trademarked modified continuous cooking process in which multiple introductions of white liquor are provided
  • EMCC refers to Kamyr, Inc.'s trademarked extended modified continuous cooking process in which a second countercurrent cook is provided.
  • Table II illustrates the advantages achieved when polysulfide is used.
  • the liquid to wood ratio for all cooks in Table II is 4/1.
  • “Sulfidity” refers to sodium sulfide content.
  • the method according to the invention optimizes the viscosity/kappa ratio and/or strength properties of kraft pulp produced, and achieves other advantageous results.
  • the utilization of polysulfide or elemental sulfur as part of the sulfide content of the white liquor also significantly increases yield.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Paper (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Catalysts (AREA)
  • Artificial Filaments (AREA)

Abstract

Paper pulp (e.g. kraft pulp or sulfite pulp) is produced utilizing at least two different supplies (35, 41) of cooking liquor (e.g. white liquor), having different percentages of lignin reaction enhancing or carbohydrate degradation slowing chemicals (e.g. one having low sulfide content, and the other high sulfide content). The high sulfide content supply is typically used to impregnate the pulp (in 37), while the second supply is used in other cooking stages (e. g. digester 12), whether co-current or countercurrent. At least 60% of the sulfide of the cooking chemicals may be provided in the first supply (35). Some of the sulfide in the first supply is desirably provided in the form of polysulfide or elemental sulfur. When about 2% polysulfide on wood is utilized yield is significantly increased. Utilizing multiple chemical (e.g. sulfide) content supplies results in an optimum viscosity/kappa ratio and/or pulp strength properties for the pulp produced. <IMAGE>

Description

    BACKGROUND AND SUMMARY OF THE INVENTION
  • The present invention relates to a method of producing kraft pulp by cooking comminuted cellulosic fibrous material with white liquor to produce kraft pulp and black liquor, whereby
    • (a) a slurry of cellulosic fibrous material is treated in a plurality of consecutive stages with white liquor, including at least first and second stages, using a first supply of white liquor to the first stage and a second supply to the second stage, the first supply of white liquor having a sulfur content greater than the sulfur content of the second supply of white liquor;
    • (b) the material treated with white liquor is subjected to cooking conditions in at least one of the stages to effect kraft cooking thereof, and black liquor is produced.
  • For many years it has been known that a higher sulfide concentration in white liquor for kraft pulping in the pulp and paper industry (i.e. higher white liquor sulfur content) could produce kraft pulp with higher viscosity and better physical properties. It has also been known that the beneficial effect of higher white liquor sulfur content is more profound in the early stages of the kraft cook than in the later stages (S. Nordén and A. Teder, Tappi, vol. 62, no. 7, July 1979, p. 49-51; B. Johannson et al, Svensk Papperstidning no. 10, 1984, p. 30-35). For improving the conditions in the initial phase S. Nordén and A. Teder describe to use two separate white liquors with different sulfidities. The higher-sulfidity liquor can be used in the impregnation and the lower-sulfidity liquor introduced later, e.g. in the transfer circulation or in the first pulping circuit. It is well-known, as dislosed in J.P. Casey "Pulp and Paper"; Chemistry and Chemical Technology 3rd ed., vol. I, 1980, John Wiley & Sons, New York, p. 470-476, that sulfur-containing gases are released during the digester relief and blow, from condensate stripping, and from other sources.
  • Several methods, including absorption in white liquor, has been proposed to treat said gases. However in the past there have been a number of technical and practical concerns and conditions which have precluded practical utilization of these concepts. Similarly maximum utilization has not been commercially made of the known ability of polysulfide to stabilize carbohydrates and wood against degradation during chemical pulping by oxidatively converting the reducing end groups in celluloses and hemi-cellulose to carboxylic groups (US-A-2,944,928).
  • According to the present invention, a method of producing kraft pulp from cellulosic comminuted fibrous material utilizing white liquor, as described above, is provided. The invention is thereby characterized by the following steps: (c) sulfur from the black liquor is recovered by heating the black liquor to produce sulfur-containing off gases; and (d) the recovered sulfur is added to a stream of white liquor made from the remaining black liquor to increase the sulfur content thereof thereby producing said first supply of white liquor deriving from said remaining black liquor.
  • In a preferred embodiment of the inventive method the off gases are treated to produce primarily methane and hydrogen sulfide. Preferably the hydrogen sulfide from the treated off gases is fed to a scrubber in which it is brought into contact with white liquor, thereby producing said first supply of white liquor so that an optimum viscosity/kappa ratio can be achieved.
  • According to the most specific aspects of the present invention, the concepts described above are utilized in a practical manner to provide kraft pulp that has an optimum viscosity/kappa ratio, and/or good strength properties, and with good yield. The invention is applicable to a wide variety of different kraft cooking processes, both batch and continuous. For example the invention can be utilized in continuous digesters having an impregnation zone, or in cooking systems utilizing a separate impregnation vessel from the continuous digester, or in batch digester. The invention can also be utilized in association with co-current movements of white liquor with the pulp, or countercurrent movements, such as are provided in the commercial digesting process marketed by Kamyr, Inc. of Glens Falls, New York under the trademark "MCC".
  • White liqour is that treatment liquid in a kraft process which contains the active cooking chemicals, sodium hydroxide (NaOH) and sodium sulfide (Na2S); or white liquor in an extreme situation may contain substantially only NaOH as active ingredient. According to standard practice, the white liquor sulfur content in the cook is maintained in the range of 25-35 % (this overall sulfur content ratio is the amount of sodium sulfide to the sum of sodium sulfide and sodium hydroxide applied to the whole cooking process), and according to standard practice in the art, a sulfur content level below 15 % results in a deterioration in the cooking rate and pulp quality. During the production of kraft pulp, residual or "black liquor" containing the reaction products of lignin solublization is whithdrawn from the digester, concentrated, and burned in a recovery furnace to yield an inorganic smelt of sodium carbonate and sodium sulfide. The smelt is dissolved to form green liquor which is reacted with quick lime (CaO) to convert the sodium carbonate into sodium hydroxide and thereby regenerate the original white liquor.
  • According to the present invention, it has been found that by making two (or more) supplies or streams of white liquor, with different sulfur contents, and applying them to different portions in the kraft cycle, significantly improved results can be achieved. In fact it has been found that it is highly desirable to add the majority of the sulfide in the total white liquor (total cooking chemical) -- at least about 60-90 %, in fact even almost all the sulfide -- at the initial stages (e.g. impregnation) of the kraft cycle, while adding white liquor with primarily only sodium hydroxide at the later stages (e.g. co-current or countercurrent cooks). Practicing the invention, it is possible to optimize the viscosity/kappa ratio of the produced pulp for any given level of sulfur content, and/or to optimize pulp strength properties. The increase can be dramatic, easily on the order of 25 % for conventional cooks with multiple white liquor additions (co-current), about the same increase for modified continuous cooking (MMC™), and 15 % or more for extended modified continuous cooking (EMMC™). Comparable increases occur for batch treatment too.
  • When about 2 % polysulfide on wood, expressed as elemental sulfur, is provided in the white liquor, a yield equal to kappa 18-20 for a conventional kraft cook is produced with a kappa of about 12.5, and pulp with a viscosity comparable to conventional cook kraft pulp at a kappa of about 26 is produced. Elemental sulfur (in dry or slurry form) may be used instead of polysulfide; elemental sulfur is about 60-75 % as effective as polysulfide.
  • While the exact source of the sulfur for producing the high sulfur content stream or supply of white liquor according to the invention is not critical as long as the sulfur is recovered according to step (c) of claim 1, one exceptionally good source that allows a practical, industrial scale process to be practiced is that shown in US-A-4,929,307 wherein sulfate black liquor is heated to above the cooking temperature so as to split the macro-molecular lignin fraction, to produce sulfur-containing off gases. Those off gases are favourably reacted to produce primarily methane and hydrogen sulfide, and then brought into contact with sulfur depleted white liquor from the normal chemical manufacturing facility of the pulp mill, to produce an extremely high sulfur content white liquor, the hydrogen sulfide being selectively absorbed into the white liquor. That high sulfur content white liquor may then be acted upon to produce at least some significant portions of polysulfide, and then utilized in early stages of the kraft cook.
  • The cooking liquor utilized above is a kraft cooking liquor. It may contain anthraquinone or its derivatives or equivalents, or the like, and the first liquor may be targeted to an impregnation stage, co-current cook stage, or countercurrent cook stage.
  • It is the primary object of the present invention to provide a substantially improved cook cycle for the production of paper pulp. This and other objects of the invention will become clear from an inspection of the detailed description of the invention, and from the appended claims.
  • BRIEF DESCRIPTION OF THE DRAWING
  • FIGURE 1 is a schematic view of exemplary apparatus for practicing an exemplary method according to the present invention.
  • DETAILED DESCRIPTION OF THE DRAWING
  • FIGURE 1 illustrates exemplary apparatus for use in kraft pulping process.
  • In a typical kraft pulping process, as illustrated in FIGURE 1, a digester 12 -- which preferably is a continuous digester such as that sold by Kamyr, Inc. of Glens Falls, New York, but may be a batch digester -- has a stream of off gases 13, and black liquor (residual white liquor containing the reaction products of lignin solubilization) is withdrawn at an intermediate position as indicated at 14, while the kraft pulp produced is discharged at 15. When the black liquor in line 14 is discharged, it may be passed directly to black liquor evaporators, and preferably it is subjected, somewhere in the evaporator chain, to a heat treatment process at step 17 to produce off gases in line 18. The heat treatment of block 17 is preferably that described in US-A-4,929,307. After heat treatment at 17 the black liquor passes to evaporators 19 (evaporator 19' may concentrate the black liquor before heat treatment 17 too), which also produce off gases in line 20, then to a conventional recovery boiler 22, with conventional white liquor manufacture at block 23, to produce white liquor in line 24 having depleted sulfur content.
  • The off gases in 18 -- which may include only those from the heat treatment 17, or also those from the digester line 13, only and from the black liquor evaporators in line 20, or a combination of any two of them -- are preferably first subjected to a drying or absorption stage (as indicated schematically at 27 in FIGURE 1) in order ro remove a majority of the water vapor. The removal of the water vapor increases the concentration of organic sulfur gases. Step 27 is accomplished by drying the gas stream by any conventional means and/or by absorbing or adsorbing the organic portion of the gas onto a solid, or additionally by absorbing the off gas into one of any non-polar liquids (e.g.kerosene or mineral oil). Treatment may be provided of a liquid mixture, but preferably according to the invention further treatment is of the concentrated gas.
  • The next steps in the treatment of the off gases as illustrated in FIGURE 1 are to add hydrogen, and the pass the gas in the presence of the added hydrogen past a hydrogen desulfurization catalyst. This may be accomplished, for example, in the hydrogen desulfurization (HDS) unit 28, with the hydrogen gas from line 29 added to the unit 28 along with the gas in line 18. The hydrogen gas in line 29 can come from any source (e.g. be purchased, from water electrolysis, etc.). It is preferred that the hydrogen desulfurization catalyst consist essentially of a transition metal-molybdenum alloy, particularly a nickel molybdenum or cobalt molybdenum alloy.
  • Typically, in gaseous processing, the product gas stream in line 30 is further acted upon. The gas stream in line 30 contains primarily methane, and hydrogen sulfide, with hydrogen also present. Preferably the hydrogen sulfide is then separated out from the gas in stream 30. While the hydrogen sulfide may be separated as a gas and then used in its gaseous form in conventional pulping techniques, it may be fed to a scrubber 32 in which it is brought into contact with a caustic solution, preferably kraft white liquor, which contains sodium hydroxide and most likely at least some sodium sulfide. While in the preferred embodiment illustrated in the drawings white liquor is utilized, under some circumstances green liquor may be advantageously utilized, with white liquor subsequently made from the green liquor.
  • White liquor from line 24 is passed into inlet 33 of scrubber 32, the hydrogen sulfide being absorbed in the white liquor and thereby significantly enhancing its sulfur content. The significantly enhanced sulfur content white liquor then passes through the outlet 34 of the scrubber into line 35, to be used in the pulping process. Desirably, the white liquor in line 35 passes through a polysulfide treatment stage, as illustrated at 36, and then to the impregnation vessel 37 (if a separate impregnation vessel is used) or the like, to be utilized in the pulping cycle. Elemental sulfur may be added at 36 instead of polysulfide.
  • The gas stream that remains, in line 38, contains primarily methane, but also some hydrogen. Ultimately, the gas in line 38 may become the source of the hydrogen for line 29.
  • According to the invention, the high sulfur content white liquor in line 35 is provided at an early stage of the cook, e.g. at the beginning of the impregnation vessel 37, or impregnation stage if impregnation takes place in the digester 12 itself, or at multiple places in the impregnation zone and/or vessel 37. A countercurrent impregnation flow may be provided, in which case the higher sulfur content liquor is added near the end of the impregnation stage. Part of the sulfide depleted white liquor in line 24 is passed into line 41, and it is then introduced into the cook, preferably at multiple locations, as indicated at 42 and 43 in FIGURE 1.
  • According to the invention, where the low sulfur content white liquor in line 41 is introduced into the kraft cook may vary widely. For example, it may be added to the middle of the impregnation vessel 37, at one, two, or more co-current stages in the digester 12, or at one, two, or more countercurrent stages in the digester 12 (e.g. for modified continuous cooking, or extended modified continuous cooking). Of course, the liquor in line 41 may also be utilized in a batch process.
  • While the drawing illustrates only two streams or supplies of white liquor, 35, 41, having different sulfur content, as many different sulfur content streams as desired may be produced. For example two series connected units 32 may be utilized, the first producing the highest sulfur content level white liquor, while the second produces an intermediate (between lines 35 and 41) sulfur content level white liquor. The intermediate sufidity white liquor is added earlier in the cook than the white liquor in line 41.
  • The relative amount of sulfur content of the white liquor added at various stages within the kraft cycle may also be varied widely according to the invention. For example, if the kraft pulping process is to be a multi-level conventional cook, that is white liquor is added at two or more points in the cook and flows co-currently with the pulp, then about 60% of the total cooking chemical is added to the impregnation vessel (e.g. in line 35), while about 25% is added to the first co-current stage (e.g. at 42) and about 15% to the second co-current stage (e.g. at 43). In this procedure, preferably the amount of sulfide provided in line 35 is about 60-90%, and if practical may be almost 100% of the total sulfide in all of the white liquor streams, that is the white liquor in stream 41 is substantially fully sulfide depleted. The stream in line 35 in this embodiment may be generated by passing 35-65% of the total volume of white liquor through the unit 32, the remaining 65-35% of the white liquor being added through line 41. According to another embodiment, about 35% of the total volume of white liquor is passed through unit 32, and this high sulfur content white liquor is then added to the top circulation in the conventional impregnation vessel 37. The sulfide-depleted white liquor in line 41 is added to middle circulation in the vessel 37 in the amount of about 25-35% of the total cooking chemical from white liquor, while about 20-25% of the total cooking chemical, in the sulfide depleted white liquor in line 41, is added to the continuous digester 12 first cooking circulation.
  • The low sodium sulfide content liquor in line 41 may also be added at 44 to an oxygen delignification or bleaching stage 45 as a source of sodium hydroxide.
  • When utilizing the multiple level sulphidity white liquors according to the invention in modified continuous cooking and extended modified continuous cooking sequences, the viscosity to kappa ratio may be increased by about 0.2-0.3 units if almost all sulfide is added to the impregnation stage (e.g. in line 35 to vessel 37). Preferably at least about 60% (e.g. 60-90%) of the total sulfur content is added in the impregnation stage (line 35), the total volume of white liquor added in line 35 being about 40-65% of the total volume of white liquor used in the pulping process.
  • In stage 36, polysulfide is added to the white liquor. For example, this can be done by the MOXY (TM) process in which some of the sodium sulfide in the white liquor is partially oxidized to produce polysulfide, or by other known polysulfide processes. Alternatively, in stage 36 polysulfide from an external source may merely be introduced into the white liquor, e.g. polysulfide produced by reacting elemental sulfur with sulfide ions in an aqueous solution under proper conditions; or elemental sulfur may be added to the white liquor instead of polysulfide.
  • The amount of polysulfide produced, or added, in stage 36 is about 0.5%-8% on wood, expressed as elemental sulfur. Typically, about 2% polysulfide is desirable. If 2% polysulfide is used in conjunction with extended modified continuous cooking, a kraft pulp with a kappa of about 12.5, a viscosity of about 33.7 cp, and a yield of about 44.6% can be made. This yield is equal to that of a conventional cook or extended modified continuous cook pulp at a kappa of about 18-20 without polysulfide, and the viscosity is equivalent to that of a conventional cook pulp at kappa 26, or an extended modified continuous cook pulp at kappa 17.
  • If an amount of elemental sulfur equivalent to about 0.5-8% polysulfide is used, the results are about 60-75% as good as when polysulfide is used.
  • Utilizing the apparatus schematically illustrated in the drawings, various methods may be practiced according to the invention. According to one method:
    • (a) Two (or more) streams of white liquor, 35, 41, are made up, the first stream (35) having relatively high sulfur content, and the second (41) relatively low sulfur content (even approaching zero).
    • (b) Cellulosic comminuted fibrous material (e.g. wood chips) are impregnated with the first stream 35 (e.g. in vessel 37).
    • (c) The material is cooked under kraft cooking conditions, in a cooking zone (in vessel 12) with cooking chemicals (the sodium hydroxide and sodium sulfide in the white liquor) to produce kraft pulp.
    • (d) The second stream, 41, of white liquor is supplied to the cooking zone (e.g. digester 12) as cooking chemicals; and
    • (e) the kraft pulp is washed (e.g. in a wash zone in digester 12, and/or in a separate wash vessel).
  • According to another aspect of the invention, a slurry of wood chips is treated in a plurality of consecutive stages (e.g. impregnation stage, first and second co-current or countercurrent cooking stages) with white liquor using first and second supplies, differing in the sulfur content thereof. The chips are treated with white liquor under cooking conditions (e.g. in digester 12) in at least one stage, to effect kraft cooking thereof. Black liquor is withdrawn (at 14) and sulfur is recovered from the black liquor, as by heating treating it (at 17) according to the process of US-A-4,929,307, evaporating it (in 19), etc. (see 22 and 23 in FIGURE 1). The recovered sulfur is added to the first supply of white liquor, as in unit 32, to significantly increase the sulfur content thereof, so that the sulfur content of the liquor in line 35 is substantially greater than that in line 24 (which is sulfur depleted, and may be near zero). The relative sulfur contents of the white liquors in lines 35 and 24 are controlled so as to optimize the viscosity/kappa ratio and/or physical strength properties.
  • The invention allows advantageous production of kraft pulp to be practiced on an industrial scale -- that is, larger production than reasonably possible in a laboratory, with complete chemical recovery.
  • The invention may be illustrated by various examples.
  • Tables IA-IE provide the results of laboratory batch cooks using split white liquor streams with variable sulfur content, according to the invention, and conventional cooks for comparison purposes. In these tables, "CK" means conventional kraft cooking, "MCK" means kraft cooking with multiple introductions of white liquor, with more than one co-current cooking stage, "MCC" refers to Kamyr, Inc.'s trademarked modified continuous cooking process in which multiple introductions of white liquor are provided, and a countercurrent cook stage, and "EMCC" refers to Kamyr, Inc.'s trademarked extended modified continuous cooking process in which a second countercurrent cook is provided.
  • Table II illustrates the advantages achieved when polysulfide is used. The liquid to wood ratio for all cooks in Table II is 4/1. "Sulfidity" refers to sodium sulfide content.
  • The wood utilized in all of TABLES IA-E and II is southern pine from the Mississippi area. However, the results are applicable to a wide variety of wood species.
    Figure imgb0001
    Figure imgb0002
    Figure imgb0003
    Figure imgb0004
    Figure imgb0005
    TABLE II
    Cook number A2961 A2958 A2962 A2959 A2960 A2963
    Type EMCC EMCC EMCC MCK MCK EMCC
    Polysulfide, % 2 2 3 2 3 nil
    PRESTEAMING:
    Time, min 5 5 5 5 5 5
    Temperature, °C 110 110 110 110 110 110
    IMPREGNATION:
    Time, min 30 30 30 30 30 30
    Temperature, °C 110 110 110 110 110 110
    Pressure, kPa (psig) 1034 (150) 1034 (150) 1034 (150) 1034 (150) 1034 (150) 1034 (150)
    Initial EA, % NaOH 12 16 13 - - 12
    Initial EA, % Na2O - - - 11.4 12.6 -
    Sulfidity, % on AA 62.5 73.6 62.5 62.5 62.5 62.8
    2nd EA @ 5 min, % NaOH 2 2 2 - - 2
    Residual EA, g/L Na2O 13.6 22.0 14.4 15.9 15.7
    Resid. polysulfide, g/L S° 1.6 1.6 1.9 2.6 -
    COCURRENT STAGE:
    Total time, min 61 60 60 73 75 60
    Max temperature, °C 164 165 164 170 170 165
    Time at max, min 45 45 45 45 45 45
    EA, % NaOH 5 5 6 - - 5
    EA, % Na2O - - - 4.75 5.25 -
    Sulfidity, % 0 0 0 0 0 0
    Residual EA, g/L Na2O 8.5 14.0 8.0 10.2 9.6
    COCURRENT STAGE II:
    Time, min. - - 135 72 -
    Temperature, °C - - 170 170 -
    EA, % Na2O - - 2.85 3.15 -
    Sulfidity, % - - 0 0 -
    COUNTERCURRENT STAGE:
    Time, min 240 240 240 - - 240
    Temperature, °C 164 160 164 - - 165
    EA, % NaOH on wood 15.3 15.4 15.4 - - 15.4
    Sulfidity, % 0 0 0 - - 0
    EA, g/L as NaOH 11.9 12.0 12.0 - - 12.0
    Displacement, L/min. 0.16 0.16 0.16 - - 0.16
    Displaced volume, L 38.4 38.4 38.4 - - 38.4
    Displacement Residual :
     @ 60 minutes, EA g/L Na2O 6.9 10.4 - -
     @ 120 minutes, EA g/L Na2O 7.6 9.1 - -
     Total Composite, EA g/L Na2O 7.3 9.6 - -
    END OF COOKING:
    Residual EA, g/L NaOH 10.0 10.0 12.4 13.4
       g/L Na2O 7.7 7.8 9.6 10.4
    H factor 2733 2239 2695 2947 1935
    UNBLEACHED PULP:
    Total yield, % 45.5 44.6 43.5 45.6
    Rejects, % 0.02 <0.01 <0.01 <0.02
    Screened yield, % 45.5 44.6 43.5 45.6
    Kappa, unscreened 17.1 12.4 15.1 11.7 15.6
    Kappa, screened 16.9 12.6 11.7 14.6
    Kappa, screened (test 2) 16.8 12.4 11.7 14.4
    Viscosity, 0.5% CED, cp 42.4 33.7 23.6 32.3
    Viscosity, (test 2) 43.7 34.5 22.0 32.4
    V/K, (test 1) 2.51 2.67 2.02 2.21
  • As can be seen from the above examples, the method according to the invention optimizes the viscosity/kappa ratio and/or strength properties of kraft pulp produced, and achieves other advantageous results. The utilization of polysulfide or elemental sulfur as part of the sulfide content of the white liquor also significantly increases yield.
  • When using other lignin reaction enhancing or carbohydrate degradation slowing chemicals, such as anthraquinone or its derivatives or equivalents, or the like, significant increases in viscosity/kappa ratio or pulp strength properties can be obtained by targeting one cooking liquor to a specific stage (or stages) of the cook, while another cooking liquor is used in other portions.

Claims (3)

  1. A method of producing kraft pulp by cooking comminuted cellulosic fibrous material with white liquor to produce kraft pulp (15) and black liquor (14), whereby
    (a) a slurry of cellulosic fibrous material is treated in a plurality of consecutive stages with white liquor, including at least first and second stages (37,12), using a first supply (35) of white liquor to the first stage and a second supply (41) to the second stage, the first supply of white liquor having a sulfur content greater than the sulfur content of the second supply (41) of white liquor;
    (b) the material treated with white liquor is subjected to cooking conditions in at least one of the stages (12) to effect kraft cooking thereof, and black liquor is produced; characterized in that
    (c) sulfur from the black liquor (14) is recovered by heating (17) the black liquor to produce sulfur-containing off gases (18); and
    (d) the recovered sulfur is added to a stream (24) of white liquor made from the remaining black liquor to increase the sulfur content thereof thereby producing said first supply (35) of white liquor deriving from said remaining black liquor.
  2. A method in accordance with claim 1, characterized in that the off gases (18) are treated to produce primarily methane and hydrogen sulfide.
  3. A method in accordance with claim 2, characterized in that the hydrogen sulfide from the treated off gases (30) is fed to a scrubber (32) in which it is brought into contact with white liquor (24), thereby producing said first supply of white liquor (35).
EP92890125A 1991-05-24 1992-05-25 A method of producing kraft pulp Expired - Lifetime EP0517689B1 (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
GB919111256A GB9111256D0 (en) 1991-05-24 1991-05-24 Pulping process
GB9111256 1991-05-24
US75684991A 1991-09-10 1991-09-10
US756849 1991-09-10
US78815191A 1991-11-05 1991-11-05
US788151 1991-11-05

Publications (2)

Publication Number Publication Date
EP0517689A1 EP0517689A1 (en) 1992-12-09
EP0517689B1 true EP0517689B1 (en) 1997-07-16

Family

ID=27265676

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92890125A Expired - Lifetime EP0517689B1 (en) 1991-05-24 1992-05-25 A method of producing kraft pulp

Country Status (6)

Country Link
EP (1) EP0517689B1 (en)
JP (1) JPH05163690A (en)
AT (1) ATE155540T1 (en)
DE (1) DE69220853D1 (en)
FI (1) FI921254A0 (en)
NO (1) NO920692L (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6132556A (en) * 1993-05-04 2000-10-17 Andritz-Ahlstrom Inc. Method of controlling pulp digester pressure via liquor extraction
US5575890A (en) * 1993-05-04 1996-11-19 Kamyr, Inc. Method for selectively increasing the sulfide ion concentration and sulfidity of kraft cooking liquor during kraft cooking of wood
FI102976B (en) * 1994-02-28 1999-03-31 Valtion Teknillinen Process for the production and use of additive cooking chemicals in one sulphate process
US5522958A (en) * 1994-07-18 1996-06-04 Pulp And Paper Research Institute Of Canada Two-stage kraft cooking
US5660686A (en) * 1994-09-02 1997-08-26 Ahlstrom Machinery Inc. Cooking with spent liquor pretreatment of cellulose material
AU2697295A (en) * 1994-09-02 1996-03-27 Kamyr Inc. Continuous kraft cooking with black liquor pretreatment
SE9703365D0 (en) * 1997-09-18 1997-09-18 Kvaerner Pulping Tech Method in connection with impregnation and digestion of lignocelulosic material
CA2307486A1 (en) * 1999-05-11 2000-11-11 Air Products And Chemicals, Inc. Use of oxidized white liquor in a kraft mill digester
US20070240837A1 (en) * 2006-04-13 2007-10-18 Andritz Inc. Hardwood alkaline pulping processes and systems
US8268124B2 (en) 2007-01-15 2012-09-18 Nihon Cellulose Co., Ltd. Method for production of pulp
JP5774025B2 (en) * 2010-01-05 2015-09-02 ビーエーエスエフ ソシエタス・ヨーロピアBasf Se Heat and fluid storage fluids for polysulfide-based extreme temperatures
FI129362B (en) * 2017-05-16 2021-12-31 Andritz Oy Method for producing chemical pulp

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992013994A1 (en) * 1991-02-06 1992-08-20 A. Ahlstrom Corporation A method of recovering energy and chemicals from black liquor

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI44743C (en) * 1962-09-15 1971-12-10 Dominon Tar & Chemical Cyclic process for the production of cellulose
US5053108A (en) * 1989-06-28 1991-10-01 Kamyr Ab High sulfidity cook for paper pulp using black liquor sulfonization of steamed chips

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992013994A1 (en) * 1991-02-06 1992-08-20 A. Ahlstrom Corporation A method of recovering energy and chemicals from black liquor

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Casey, J.P., "Pulp and Paper; Chemistry and Chemical Technology - 3rd edition, vol. I", 1980, John Wiley & Sons, Inc., New York, pages 470-476. *
Tappi, vol. 62, no. 7, July 1979, Atlanta, US, pages 49-51, Nordén S. et al *

Also Published As

Publication number Publication date
JPH05163690A (en) 1993-06-29
ATE155540T1 (en) 1997-08-15
NO920692L (en) 1992-11-25
DE69220853D1 (en) 1997-08-21
FI921254A0 (en) 1992-03-24
EP0517689A1 (en) 1992-12-09
NO920692D0 (en) 1992-02-21

Similar Documents

Publication Publication Date Title
CA1222603A (en) Polution free pulping process using recycled wash effluent from multiple bleach stages to remove black liquor and recovering sodium hydroxide from the black liquor
US5779856A (en) Cooking cellulose material using high alkali concentrations and/or high pH near the end of the cook
CA2651483C (en) Methods for carbonate pretreatment and pulping of cellulosic material
EP0517689B1 (en) A method of producing kraft pulp
JPH09507697A (en) Production of pre-hydrolyzed pulp
JPS6012477B2 (en) Continuous alkaline delignification method for lignocellulose materials
US3691008A (en) Two-stage soda-oxygen pulping
US4045279A (en) Process for the manufacture of pulp using sodium carbonate and oxygen
JP7292296B2 (en) Dissolving pulp manufacturing method
EP0519061B1 (en) Split alkali addition for high consistency oxygen delignification
US6143130A (en) Polysulfide pulping process
US20060102300A1 (en) Alkaline process for the manufacturing of pulp using alkali metaborate as buffering alkali
US5326433A (en) Multi-level sulfide content white liquor production and utilization in cellulose pulping
US5340440A (en) Method for recovering chemicals using recovery boiler having at least 2 different melt sections
EP0635080B1 (en) Method of producing pulp
NZ199486A (en) Process for chemimechanical pulp production;using alkaline peroxide liquor
EP0584161B1 (en) White liquor preparation and pulping process
WO1995032331A1 (en) Sulphidic impregnation of chips for alkaline pulping
US5525195A (en) Process for high consistency delignification using a low consistency alkali pretreatment
US3520773A (en) Alkaline pulping processes with chemical pretreatment
EP0530881A1 (en) Use of wash press for pulp alkali addition process
CA2069281C (en) Multi-level sulfide content pulping
EP0540091A1 (en) Wash press modification for oxygen delignification process
CA2189899C (en) Cooking cellulose material using high alkali concentrations and/or high ph near the end of the cook
AU3256001A (en) Pulping process

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU MC NL PT SE

17P Request for examination filed

Effective date: 19930305

17Q First examination report despatched

Effective date: 19940426

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: AHLSTROM MACHINERY INC.

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU MC NL PT SE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19970716

Ref country code: LI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19970716

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 19970716

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19970716

Ref country code: FR

Effective date: 19970716

Ref country code: ES

Free format text: THE PATENT HAS BEEN ANNULLED BY A DECISION OF A NATIONAL AUTHORITY

Effective date: 19970716

Ref country code: DK

Effective date: 19970716

Ref country code: CH

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19970716

Ref country code: BE

Effective date: 19970716

Ref country code: AT

Effective date: 19970716

REF Corresponds to:

Ref document number: 155540

Country of ref document: AT

Date of ref document: 19970815

Kind code of ref document: T

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REF Corresponds to:

Ref document number: 69220853

Country of ref document: DE

Date of ref document: 19970821

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Effective date: 19971017

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Effective date: 19971022

NLV1 Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act
EN Fr: translation not filed
REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980525

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980525

26N No opposition filed
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19981130

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19980525

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 20020418

Year of fee payment: 11

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20030526

EUG Se: european patent has lapsed