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US20110056637A1 - Prehydrolysis sulfate cooking process - Google Patents

Prehydrolysis sulfate cooking process Download PDF

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Publication number
US20110056637A1
US20110056637A1 US12/991,554 US99155409A US2011056637A1 US 20110056637 A1 US20110056637 A1 US 20110056637A1 US 99155409 A US99155409 A US 99155409A US 2011056637 A1 US2011056637 A1 US 2011056637A1
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US
United States
Prior art keywords
pressure
digester
pressure reduction
bar
cellulosic material
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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.)
Abandoned
Application number
US12/991,554
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English (en)
Inventor
Olavi Katajisto
Lari Lammi
Antti Viro
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Valmet Technologies Oy
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Metso Paper Oy
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
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Assigned to METSO PAPER, INC. reassignment METSO PAPER, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KATAJISTO, OLAVI, LAMMI, LARI, VIRO, ANTTI
Publication of US20110056637A1 publication Critical patent/US20110056637A1/en
Assigned to VALMET TECHNOLOGIES, INC. reassignment VALMET TECHNOLOGIES, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: METSO PAPER, INC.
Abandoned legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C1/00Pretreatment of the finely-divided materials before digesting
    • D21C1/02Pretreatment of the finely-divided materials before digesting with water or steam
    • 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
    • D21C1/00Pretreatment of the finely-divided materials before digesting
    • D21C1/10Physical methods for facilitating impregnation
    • 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

Definitions

  • the present invention relates to an improved prehydrolysis sulfate (Kraft) cooking process.
  • An improved method is disclosed for terminating the hydrolysis stage of the prehydrolysis sulfate cooking process. More precisely, the invention relates to termination of the hydrolysis stage operating in the steam phase, wherein such termination is also performed in the steam phase.
  • the prehydrolysis-sulfate (Kraft) cooking for the production of special pulps having a high content of alpha cellulose was developed in the 1930's, see e.g. Rydholm, S. E., Pulping Processes, pp. 649 to 672, Interscience Publishers, New York, 1968.
  • the basic idea was to remove as much hemicellulose as possible from cellulose fibers in connection with delignification, so as to obtain a high content of alpha cellulose. This is essential because the various end uses of such pulps, dissolving pulp for instance, do not tolerate short-chained hemicellulose molecules with a randomly grafted molecular structure.
  • a separate prehydrolysis step permits the desired adjustment of the hydrolysis of hemicelluloses by varying the hydrolysis conditions.
  • the prehydrolysis is carried out either as a water or steam phase prehydrolysis, or in the presence of a catalyst.
  • organic acids liberated from wood during the process perform a major part of the hydrolysis
  • small amounts of mineral acid or sulfur dioxide are added to “assist” the prehydrolysis.
  • direct steam is introduced to the chip column in the digester. Due to the material and energy balance, very little, if any, liquid hydrolysate phase is generated, as all condensate is trapped in the porosity of the wood material.
  • the hydrolysate and the prehydrolyzed cellulosic material are neutralized in the reactor with alkaline neutralizing liquor so as to produce neutralized hydrolysate and neutralized prehydrolyzed cellulosic material.
  • hydrolysate both in the free liquid outside the chips and also trapped and immobilized inside the chips. If desired, part of the hydrolysate can be recovered before the neutralization step.
  • the neutralization step the contents of the digester are prepared for later delignification, to be carried out by alkaline kraft cooking.
  • the prehydrolyzed material is conventionally neutralized with alkali-containing liquid, either by displacement or circulation.
  • Neutralization is achieved by selecting an appropriate neutralizing alkali charge, which results in a clear alkaline neutralization end point.
  • Suitable neutralizing agents to be used contain caustic soda, and the preferred agent is alkaline Kraft cooking liquor, i.e., white liquor.
  • the displacement process can be performed, for example, by filling up the digester with white liquor so that the leading edge of the white liquor neutralizes the hydrolysate.
  • alkali-containing liquid is pumped into the digester so as to displace the hydrolysate from outside the chips.
  • Neutralization is completed by circulating the liquid in the digester and thus mixing the contents therewith.
  • the neutralization step also serves as an alkaline hemicellulose-dissolving step.
  • the strong alkali and the high temperature directly dissolve and, on the other hand, degrade hemicellulose by the so-called end-wise peeling reaction.
  • the pulp is thus further purified, which leads to higher pulp viscosity and higher alpha cellulose content.
  • the neutralization step also becomes, in part, an alkaline extraction stage prior to the cooking step. Therefore, the liquor-to-wood ratio in this step is preferably relatively low, such as between about 2.5 and 3.5.
  • the neutralized prehydrolyzed cellulosic material is delignified with alkaline cooking liquor (containing sodium sulfide and sodium hydroxide).
  • alkaline cooking liquor containing sodium sulfide and sodium hydroxide.
  • the delignification step has been a conventional Kraft cooking method, where white liquor has been added to the digester and the cooking has been carried out as a single step.
  • the acidic hydrolysis stage of the prehydrolysis sulfate (Kraft) cooking of the prior art is terminated (i.e. neutralized) e.g. by filling up the digester with white liquor or with some other alkali-containing liquid to effect the pH change and to be able to transfer from the acidic hemicellulose-splitting condition/state to an alkaline lignin-dissolving sulfate cooking state.
  • the neutralization i.e. termination of the hydrolysis stage, is performed in the same way independently of whether or not the prehydrolysis is operated in a liquid or in a steam phase.
  • Both of the above-mentioned neutralization methods i.e. circulation and displacement are time-consuming, which makes the uniformity of the neutralization poorer.
  • the alkaline liquid comprises a white liquor.
  • the at least one addition of the alkaline liquid comprises a single addition of the alkaline liquid at the first pressure
  • the at least one pressure reduction comprises a single pressure reduction to a second pressure lower than the first pressure.
  • the first pressure comprises a pressure of between about 6 and 9 bar
  • the second pressure comprises a pressure of between about 3 and 5 bar.
  • the single pressure reduction is carried out for a period of about 1 second to about 10 minutes, preferably from about 30 seconds to about 5 minutes.
  • the at least one addition of the alkaline liquid comprises a single addition of the alkaline liquid
  • the at least one pressure reduction comprises a gradual pressure reduction.
  • the first pressure comprises a pressure of between about 6 and 9 bar
  • the gradual pressure reduction comprises a gradual pressure reduction from the first pressure to a second pressure
  • the second pressure comprising a pressure of between about 3 and 5 bar
  • the gradual pressure reduction is carried out by reducing the pressure in increments of from about 0.5 to 2 bar.
  • One object of the present invention is to provide an improved process for the preparation of pulp from lignin-containing cellulosic material, in which the prehydrolysis is carried out in a steam phase and the termination (i.e. neutralization of the contents of the digester) of the prehydrolysis stage is also carried out in a steam phase in order to overcome many of the problems associated with the prior art.
  • steam phase termination is carried out by adding alkaline liquid in a prevailing pressure into the digester and then temporarily reducing the pressure of the digester. As a result of the pressure reduction the added alkaline liquid evaporates to the gas space of the digester, thus neutralizing the prehydrolyzed material in the digester.
  • the present invention is directed to a process for the preparation of prehydrolyzed pulp in a digester from lignin-containing cellulosic material comprising
  • the prehydrolysis stage is carried out in a steam phase, by introducing direct steam to the chip column in the digester at a temperature of from about 150 to 180° C., preferably at a temperature of 160 to 170° C.
  • the steaming is normally initiated with a low-pressure steam (LP; appr. 3.5 bar, 150° C.) and then continued with a medium pressure steam (MP; appr. 10.5 bar, 200° C.) until the desired temperature in the venting line of the digester is obtained, i.e. the temperature of the digester contents is about 150 to 180° C.
  • the temperature inside the digester is measured from the temperature of the venting gas in the venting line.
  • the pressure inside the digester can vary between about 4.8 bar and 10.0 bar, preferably it is in the range of from about 6 to about 9 bar.
  • a suitable prehydrolyzing time is from about 10 to 200 minutes, preferably from about 20 to 120 minutes.
  • the contents of the digester are neutralized, i.e. the prehydrolysis stage is terminated by a termination stage, which stage comprises at least one addition of an alkaline liquid at a prevailing pressure (i.e. at a first pressure) followed by at least one pressure reduction to a second pressure.
  • a termination stage which stage comprises at least one addition of an alkaline liquid at a prevailing pressure (i.e. at a first pressure) followed by at least one pressure reduction to a second pressure.
  • the first pressure is always higher than the second pressure.
  • the pressure difference between the first pressure and the second pressure i.e. the magnitude of the pressure drop, depends on several process variables, e.g. strength of the alkali, degree of packing and pressure of the digester.
  • the pressure of the digester is reduced so that the alkali charged/introduced evaporates and thus neutralizes the prehydrolyzed material in the digester.
  • This termination stage can also be called a neutralization stage, as the acidic prehydrolyzed material is neutralized during this step.
  • the amount of alkali thus charged is determined so that all of the liquid (free liquid outside the chips and liquid trapped and immobilized inside the chips) in the digester is neutralized, and alkaline conditions are obtained that are at a pH of 7 or greater.
  • a suitable alkaline liquid for example alkalized black liquor, preferably white liquor
  • the first pressure is the pressure of the end of the prehydrolysis stage, i.e. between 4.8 bar and 10.0 bar, preferably in the range of from about 6 bar to about 9 bar.
  • the pH of the digester contents cannot be directly measured, thus, normally, the alkaline conditions are ensured by feeding some extra amount of alkaline liquid into the digester.
  • the pressure of the digester is momentarily reduced from the first pressure to a second pressure, which is from about 2 to 7 bar, preferably from about 3 to 5 bar.
  • the pressure is reduced for a period of about 1 second to 10 minutes, preferably for a period of about 30 seconds to 5 minutes.
  • an alkaline delignifying step In the delignifying step the digester is filled up with the cooking chemicals, the temperature is increased to the cooking temperature, which is maintained until the desired degree of delignification is obtained.
  • the pressure reduction of the termination stage is performed gradually.
  • suitable alkaline liquid for example alkalized black liquor, preferably white liquor
  • the pressure is reduced gradually step-by-step, for example, at increments of about 0.5 to 2 bar at a time, to obtain the end pressure, which is from about 2 to 7 bar, preferably from about 3 to 5 bar.
  • the digester is filled up with the cooking chemicals and thus preparation of the pulp is continued by an alkaline delignifying step.
  • the total amount of the needed (2to 15% as NaOH on wood) suitable alkaline liquid for example alkalized black liquor, preferably white liquor, is gradually added into the digester and after each addition the pressure is reduced from the previous pressure.
  • suitable alkaline liquid for example alkalized black liquor, preferably white liquor
  • the pressure is reduced for a suitable period of time, i.e. for a period of about 1 second to 10 minutes, preferably for a period of about 30 seconds to 5 minutes.
  • the rest of the alkaline liquid is added into the digester followed by a second pressure drop.
  • the amount of alkaline liquid needed can also be added in more than two batches.
  • Each addition of alkaline liquid is followed by a pressure reduction.
  • the pressure can be reduced e.g. gradually so that after the addition of alkaline liquid the reduction of the pressure is in increments of from about 0.5 to 1 bar, preferably from about 0.5 to 0.7 bar from the previous pressure.
  • the neutralizing liquid is preferably introduced into the digester through the bottom of the digester, but other possible methods are also within the scope of the present invention.
  • the prehydrolyzed cellulosic material is delignified by conventional sulfate cooking.
  • the cooking chemicals e.g. white liquor and spent black liquor
  • the digester contents are then heated by direct steam or by means of indirect heating of the recirculating pulping liquor in a heat exchanger.
  • a suitable cooking temperature is from about 150° C. to 180° C., preferably from about 150° C. to 165° C. for hardwoods, and from about 155° C. to 170° C. for softwoods.
  • the digester contents are blown to a blow tank.

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  • Paper (AREA)
US12/991,554 2008-05-08 2009-05-06 Prehydrolysis sulfate cooking process Abandoned US20110056637A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FI20085425A FI20085425A7 (fi) 2008-05-08 2008-05-08 Sulfaattiesihydrolyysikeittomenetelmä
FI20085425 2008-05-08
PCT/FI2009/050364 WO2009136000A1 (fr) 2008-05-08 2009-05-06 Procédé au sulfate avec préhydrolyse

Publications (1)

Publication Number Publication Date
US20110056637A1 true US20110056637A1 (en) 2011-03-10

Family

ID=39523080

Family Applications (1)

Application Number Title Priority Date Filing Date
US12/991,554 Abandoned US20110056637A1 (en) 2008-05-08 2009-05-06 Prehydrolysis sulfate cooking process

Country Status (5)

Country Link
US (1) US20110056637A1 (fr)
EP (1) EP2286022A1 (fr)
CN (1) CN102016162A (fr)
FI (1) FI20085425A7 (fr)
WO (1) WO2009136000A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020236061A1 (fr) * 2019-05-22 2020-11-26 Valmet Ab Procédé d'extraction d'hydrolysat, système de cuisson par lots et agencement d'extraction d'hydrolysat

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2567023B1 (fr) * 2010-05-04 2014-10-15 Bahia Specialty Cellulose SA Méthode et système pour la production de pâte à haute teneur en cellulose alpha
AU2010202496B2 (en) * 2010-05-04 2015-04-16 Bahia Specialty Cellulose Sa Method and system for high alpha dissolving pulp production
KR20110123184A (ko) 2010-05-06 2011-11-14 바히아 스페셜티 셀룰로스 에스에이 높은 알파 용해 펄프 제조를 위한 방법 및 시스템
CA2837277C (fr) * 2011-05-13 2017-06-27 Metso Paper Sweden Ab Procede compact d'obtention de pate prealablement hydrolysee
CN102337693B (zh) * 2011-09-30 2014-01-22 重庆理文造纸有限公司 一种溶解浆的蒸煮及洗涤工艺
WO2017142445A1 (fr) * 2016-02-16 2017-08-24 Valmet Ab Procédé de récupération d'hydrolysat concentré après l'hydrolyse de matière de cellulose
WO2019039982A1 (fr) * 2017-08-25 2019-02-28 Valmet Ab Procédé compact amélioré pour la production d'une pâte préhydrolysée
CN108252141A (zh) * 2018-01-04 2018-07-06 安徽工程大学 一种蔺草纤维及其湿法非织造织物的制备方法

Citations (4)

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Publication number Priority date Publication date Assignee Title
US3013933A (en) * 1953-01-28 1961-12-19 Rayonier Inc Method for preparation of wood cellulose
US5198074A (en) * 1991-11-29 1993-03-30 Companhia Industreas Brasileiras Portela Process to produce a high quality paper product and an ethanol product from bamboo
US5203963A (en) * 1991-10-21 1993-04-20 A. Ahlstrom Corporation Continuous treatment of small chips
US5676795A (en) * 1992-12-02 1997-10-14 Voest-Alpine Industrieanlagenbau Gmbh Process for the production of viscose pulp

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GB758766A (en) * 1954-05-10 1956-10-10 Brown And Root Inc Process for the production of pulp from bagasse
SE523850E (sv) * 1997-09-22 2009-06-02 Metso Fiber Ab Förfarande vid förbehandling av flis med basningsånga och impregneringsvätska
DE19856582C1 (de) * 1998-12-08 2001-03-15 Rhodia Acetow Ag Verfahren zur Gewinnung von Chemiezellstoff aus Hackschnitzeln
SE0104272L (sv) * 2001-12-17 2002-11-12 Kvaerner Pulping Tech Förfarande och arrangemang vid impregnering av flis
CA2610797C (fr) 2005-06-03 2014-08-05 Iogen Energy Corporation Procede de traitement en continu de matieres premieres lignocellulosiques
FI123036B (fi) * 2006-02-10 2012-10-15 Metso Paper Inc Menetelmä hydrolyysituotteiden talteenottamiseksi

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3013933A (en) * 1953-01-28 1961-12-19 Rayonier Inc Method for preparation of wood cellulose
US5203963A (en) * 1991-10-21 1993-04-20 A. Ahlstrom Corporation Continuous treatment of small chips
US5198074A (en) * 1991-11-29 1993-03-30 Companhia Industreas Brasileiras Portela Process to produce a high quality paper product and an ethanol product from bamboo
US5676795A (en) * 1992-12-02 1997-10-14 Voest-Alpine Industrieanlagenbau Gmbh Process for the production of viscose pulp

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Efunda, Saturated Steam Tables, 140, 150, and 170 degrees C, downloaded online 9/5/2012. *
Gullichsen editor, Chemical Pulping 6A, 1999, Fapet Oy, pg. 60-64. *
Sixta Herbert editor, Handbook of Pulp, 2006, Wiley-VCH Verlag GmbH and Co., pg. 229-365. *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020236061A1 (fr) * 2019-05-22 2020-11-26 Valmet Ab Procédé d'extraction d'hydrolysat, système de cuisson par lots et agencement d'extraction d'hydrolysat
CN113811650A (zh) * 2019-05-22 2021-12-17 维美德公司 提取水解产物的方法、间歇蒸煮系统和水解产物提取装置

Also Published As

Publication number Publication date
EP2286022A1 (fr) 2011-02-23
FI20085425L (fi) 2009-11-09
FI20085425A7 (fi) 2009-11-09
WO2009136000A1 (fr) 2009-11-12
CN102016162A (zh) 2011-04-13
FI20085425A0 (fi) 2008-05-08

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Legal Events

Date Code Title Description
AS Assignment

Owner name: METSO PAPER, INC., FINLAND

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KATAJISTO, OLAVI;LAMMI, LARI;VIRO, ANTTI;REEL/FRAME:025585/0819

Effective date: 20101018

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION

AS Assignment

Owner name: VALMET TECHNOLOGIES, INC., FINLAND

Free format text: CHANGE OF NAME;ASSIGNOR:METSO PAPER, INC.;REEL/FRAME:032551/0426

Effective date: 20131212