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EP0863250A2 - Procede de preparation d'une liqueur de cuisson permettant d'obtenir un produit semi-fini fibreux - Google Patents

Procede de preparation d'une liqueur de cuisson permettant d'obtenir un produit semi-fini fibreux Download PDF

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Publication number
EP0863250A2
EP0863250A2 EP96940192A EP96940192A EP0863250A2 EP 0863250 A2 EP0863250 A2 EP 0863250A2 EP 96940192 A EP96940192 A EP 96940192A EP 96940192 A EP96940192 A EP 96940192A EP 0863250 A2 EP0863250 A2 EP 0863250A2
Authority
EP
European Patent Office
Prior art keywords
pulp
waste water
weight
cooking
activated sludge
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP96940192A
Other languages
German (de)
English (en)
Other versions
EP0863250A4 (fr
Inventor
Vladimir Pavlovich Grudinin
Alexandr Vladimirovich Grudinin
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.)
Pukanov Vitaly Valerievich
Original Assignee
Pukanov Vitaly Valerievich
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 Pukanov Vitaly Valerievich filed Critical Pukanov Vitaly Valerievich
Publication of EP0863250A2 publication Critical patent/EP0863250A2/fr
Publication of EP0863250A4 publication Critical patent/EP0863250A4/fr
Withdrawn legal-status Critical Current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
    • D21C11/00Regeneration of pulp liquors or effluent waste waters
    • D21C11/0021Introduction of various effluents, e.g. waste waters, into the pulping, recovery and regeneration cycle (closed-cycle)
    • 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
    • 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
    • D21C3/04Pulping cellulose-containing materials with acids, acid salts or acid anhydrides
    • D21C3/06Pulping cellulose-containing materials with acids, acid salts or acid anhydrides sulfur dioxide; sulfurous acid; bisulfites sulfites

Definitions

  • the proposed invention deals with pulp and paper production, in particular, with the process for preparing pulp cooking liquors to manufacture a fibrous semifabricate.
  • a method for preparing a pulp cooking liquor by adding a sulfate into a water medium is known (1).
  • the closest to the proposed invention is a well known method for preparing a cooking liquor to manufacture a fibrous semifabricate.
  • the method in question requires waste water that has been treated biologically be used as a water medium.
  • This waste water that normally contains an excessed activated sludge in the range of 0,5 - 17,0 g/l is to be withdrawn from a secondary thickener to dissolve sulfates.
  • sulfite or bisulfite cooking methods are used the abovementioned water medium is to be saturated with sulfurous anhydride until the required pH value is reached (4).
  • This method may offer cost advantages resulting from replacement fresh water with waste one after biological treatment thereof.
  • this method leads to a comparatively low pulp yield and doesn't secure that the required level of its quality parameters needed now will be reached.
  • waste water at low activated sludge concentration is used as a water medium here.
  • the proposed invention is aimed at creating a method for preparing a pulp cooking liquor to manufacture a fibrous semifabricate in a way that makes it possible to increase the yield of the final product, improve its quality as well as to extend a stock of row materials needed for preparing sulfite cooking liquors.
  • soda ash (1,5 - 2,50 % by weight based on Na 2 O) in form of a solution in biologically treated effluents of pulp and paper manufacture which in turn run between 18 and 40 g/l suspended solids or alkaline hydrolizate generated at the treatment of the same effluents by a mixture of basic salts (both Na 2 CO 3 - 50 - 90 % by weight and CaO - 1,5 - 2,5 % by weight based on Na 2 O) at the temperature of 25 - 40°C accompanied by removal of resulting precipitate are used as water medium while saturating thereof with sulfurous anhydride at 35-40°C until its content in the cooking liquor is 2,2-5,5 % by weight based on the total mass of the solution.
  • basic salts both Na 2 CO 3 - 50 - 90 % by weight and CaO - 1,5 - 2,5 % by weight based on Na 2 O
  • the proposed method differs from the well known one by the following features: soda ash (1,5 - 2,50 % by weight based on Na 2 O) in form of a solution in biologically treated effluents of pulp and paper manufacture running between 18 and 40 g/l suspended solids or alkaline hydrolizate generated at the treatment of the same effluents by a mixture of basic salts (Na 2 CO 3 - 50 - 90% by weight and CaO - 1,5 - 2,5 % by weight based on Na 2 O) at 25 - 40°C accompanied by removal of resulting precipitate are used as a water medium.
  • the proposed method means the use of industrial waste water after biological treatment with concentration of activated sludge biomass in the range of 18 - 40g/l.
  • concentration of activated sludge biomass in the range of 18 - 40g/l.
  • concentration obtained by preliminary consolidation of activated sludge biomass in special settlers is optimal since it mantains higher than usual content of acid and alkali hydrolysis products in a cooking liquor that are formed during its preparation and thus, as it has been mentioned, making cooking more effective.
  • the usage of industrial waste water with high concentration of activated sludge (18-40g/l) allows to utilize activated sludge biomass.
  • alkali hydrolyzate as a water medium allows to get rid effectively (by means of co-precipitation with calcium carbonate) from a non-hydrolized part of activated sludge biomass, which makes up to 17% by weight based on absolutely dry substance thus improving the quality characteristics required for a fibrous semi-fabricate.
  • the proposed conditions for alkali hydrolizate production (treatment by mixed base salts containing 50-90% of sodium carbonate by weight and 10-15% of calcium oxide by weght in amount of 1,55-2,50% by weight based on Na 2 O at the temperature 25-40°C followed up with removal of sediment) makes it possible to reach a complete alkali hydrolysis of bio-organic part of activated sludge and to remove an insoluble slime. All this in turn, increases the efficiency of cooking process and makes the quality of the fibrous semi-fabricate better.
  • the method is carried out in the following way:
  • Sodium carbonate (in amount that makes its concentration in solution equal to 1,55-2,50% by weight based on Na 2 O) is added to biologically treated waste water of a pulp and paper mill after settling thereof in a radial or vertical thickener until the activated sludge concentration in it has reached the level of 18-40g/l.
  • the resultant soda ash solution is sent to an absorber for saturation with sulfurous anhidride at the temperature 35-45°C until its concentration is of 2,5-5,5% by weight and organic part of the sludge is dissolved.
  • a pulp and paper mill waste water that has been treated biologically and then stored in a thickener until the excessed activated sludge concentration in it has reached the level of 18-40g/l is delivered to a mixer to be treated with a mixed base salts in amount of 1,55-2,50% by weight based on Na 2 O at the temperature of 25-40°C provided that it is accompanied by thorough mixing until the activated sludge biomass is dissolved completely.
  • the resulting mixture containing alkali hydrolizate, undissolved slime and calcium carbonate is to be dewatered by filtration or precipitation.
  • the resultant clarified alkali hydrolyzate is sent to an absorber for saturation with sulfurous anhydride at the temperature of 35-45°C until the concentration thereof is 2,5-5,5% by weight is reached.
  • the metod is illustrated by the following examples:
  • the cooking process was carried out during 2 hours 15 minutes while the temperature being raised from 25°C to 100°C; then during 45 minutes the temperature was kept at 120°C and during another 1 hour and a half it had been raising from 120°C to 160°C. Then the process proceeded at that temperature (160°C) for another 1 hour.
  • the cooking is over a 75g/l sample of the resultant semifabricate was used to determine both its whiteness and mechanical characteristics. The results obtained are given in the Table.
  • the cooking liquor was prepared in the following way: The waste water from a pulp and paper mill with activated sludge making up 30g/l in it was treated by a mixed base containing the equal parts of sodium carbonate and calcium oxide in amount of 2,5% by weight based on Na 2 O at the temperatute 35°C. After the sediment had been removed the alkali hydrolyzate was saturated with sulfurous anhydride at the temperature 40°C until the concentration thereof was reached 5,5% by weight. The resultant cooking liquor with products yielded by the alkali hydrolysis of activated sludge had 1,9 pH value. The cooking process was carried out under the same conditions as it was in the Example 1. The results are given in the Table.
  • the cooking process is held in conditions of Example 1.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Paper (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
EP96940192A 1995-11-21 1996-11-13 Procede de preparation d'une liqueur de cuisson permettant d'obtenir un produit semi-fini fibreux Withdrawn EP0863250A4 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
RU95119640 1995-11-21
RU9595119640A RU2091529C1 (ru) 1995-11-21 1995-11-21 Способ приготовления варочного раствора для получения волокнистого полуфабриката
PCT/RU1996/000323 WO1997019220A2 (fr) 1995-11-21 1996-11-13 Procede de preparation d'une liqueur de cuisson permettant d'obtenir un produit semi-fini fibreux

Publications (2)

Publication Number Publication Date
EP0863250A2 true EP0863250A2 (fr) 1998-09-09
EP0863250A4 EP0863250A4 (fr) 1998-11-25

Family

ID=20173977

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96940192A Withdrawn EP0863250A4 (fr) 1995-11-21 1996-11-13 Procede de preparation d'une liqueur de cuisson permettant d'obtenir un produit semi-fini fibreux

Country Status (10)

Country Link
EP (1) EP0863250A4 (fr)
JP (1) JP2000500538A (fr)
KR (1) KR19990071498A (fr)
CN (1) CN1207782A (fr)
AU (1) AU7713796A (fr)
BR (1) BR9611644A (fr)
CA (1) CA2238100A1 (fr)
NO (1) NO982293L (fr)
RU (1) RU2091529C1 (fr)
WO (1) WO1997019220A2 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108017790B (zh) * 2017-12-13 2018-12-07 济南圣泉集团股份有限公司 一种生产高活性木质素和副产糠醛的方法及应用

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1432245A (en) * 1972-05-01 1976-04-14 Westvaco Corp Method of pulping wood
FR2184608B1 (fr) * 1972-05-15 1975-04-04 Owens Illinois Inc
GB1433307A (en) * 1974-07-11 1976-04-28 Texaco Development Corp Integrated kraft pulping process
US4155804A (en) * 1975-03-17 1979-05-22 International Telephone And Telegraph Corporation Removal of volatile organic components from spent sulfite effluent
DE2640885C3 (de) * 1975-09-16 1979-02-22 Pwa Papierwerke Waldhof-Aschaffenburg Ag, 8000 Muenchen Verfahren zur Herstellung von Zellstoff nach dem Sulfitverfahren
SU746002A1 (ru) * 1978-05-30 1980-07-07 Всесоюзное научно-производственное объединение целлюлозно-бумажной промышленности Варочный раствор дл получени волокнистого полуфабриката
SU783386A1 (ru) * 1978-07-17 1980-11-30 Всесоюзное научно-производственное объединение целлюлозно-бумажной промышленности Варочный раствор дл получени волокнистого целлюлозосодержащего полуфабриката
SU896125A1 (ru) * 1980-05-14 1982-01-07 Центральный научно-исследовательский институт бумаги Способ получени целлюлозы
SU903417A1 (ru) * 1980-05-26 1982-02-07 Всесоюзное научно-производственное объединение целлюлозно-бумажной промышленности Способ получени целлюлозы дл химической переработки
FI67105C (fi) * 1980-11-14 1985-02-20 Rauma Repola Oy Foerfarande foer framstaellning av kokvaetska erforderilig i neutralsulfitkok med antrakinonoekning
SU1074929A1 (ru) * 1982-10-19 1984-02-23 Всесоюзное Ордена Трудового Красного Знамени Научно-Производственное Объединение Целлюлозно-Бумажной Промышленности Способ приготовлени сульфитной варочной кислоты дл производства целлюлозы
SU1164347A1 (ru) * 1984-01-03 1985-06-30 Ленинградская Ордена Ленина Лесотехническая Академия Им.С.М.Кирова Способ получени целлюлозы
SU1608274A1 (ru) * 1988-01-21 1990-11-23 Ленинградская лесотехническая академия им.С.М.Кирова Способ приготовлени сульфитной варочной жидкости дл получени целлюлозы дл химической переработки

Also Published As

Publication number Publication date
EP0863250A4 (fr) 1998-11-25
CN1207782A (zh) 1999-02-10
RU2091529C1 (ru) 1997-09-27
BR9611644A (pt) 1999-07-13
CA2238100A1 (fr) 1997-03-29
NO982293D0 (no) 1998-05-20
WO1997019220A3 (fr) 1997-08-14
NO982293L (no) 1998-07-20
WO1997019220A2 (fr) 1997-05-29
JP2000500538A (ja) 2000-01-18
AU7713796A (en) 1997-06-11
KR19990071498A (ko) 1999-09-27

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