WO1998056988A1 - A PROCESS FOR STABILIZING THE pH OF A PULP SUSPENSION AND FOR PRODUCING PAPER FORM THE STABILIZED PULP - Google Patents

A PROCESS FOR STABILIZING THE pH OF A PULP SUSPENSION AND FOR PRODUCING PAPER FORM THE STABILIZED PULP Download PDF

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Publication number
WO1998056988A1
WO1998056988A1 PCT/FI1998/000509 FI9800509W WO9856988A1 WO 1998056988 A1 WO1998056988 A1 WO 1998056988A1 FI 9800509 W FI9800509 W FI 9800509W WO 9856988 A1 WO9856988 A1 WO 9856988A1
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WO
WIPO (PCT)
Prior art keywords
pulp suspension
pulp
carbon dioxide
process according
alkali metal
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.)
Ceased
Application number
PCT/FI1998/000509
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English (en)
French (fr)
Inventor
Hannu Juhani Leino
Anna Linnea Holmberg
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.)
Linde Sverige AB
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AGA AB
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.)
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Publication date
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Priority to CA002293405A priority Critical patent/CA2293405C/en
Priority to EP98925673A priority patent/EP0991811B1/en
Priority to AU77696/98A priority patent/AU731377B2/en
Priority to AT98925673T priority patent/ATE204936T1/de
Priority to JP50168899A priority patent/JP2002504193A/ja
Application filed by AGA AB filed Critical AGA AB
Priority to DE69801504T priority patent/DE69801504T2/de
Priority to US09/445,710 priority patent/US6991705B2/en
Priority to DE0991811T priority patent/DE991811T1/de
Publication of WO1998056988A1 publication Critical patent/WO1998056988A1/en
Priority to NO19996070A priority patent/NO328511B1/no
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/63Inorganic compounds
    • D21H17/64Alkaline compounds

Definitions

  • the invention relates to a process for stabilizing the pH of a paper making pulp suspension with buffering agents and to a process for producing paper from such a stabilized pulp suspension.
  • neutral pH corresponds in these processes to a pH in the short circulation of approximately 7-8,5, most preferably 7-8. This applies to paper produced from chemical, mechanical and recycled pulp, bleached or unbleached.
  • the traditional way of raising and controlling the pH is to add sodium hydroxide, NaOH.
  • NaOH is, however, a very strong base, which means that only small amounts are needed for pH adjustments. Any over-dosage will cause a too big pH increase, which means that it is difficult to perform the pH adjustment in a controlled way. This is due to the low inherent buffering ability of a pulp suspension. The paper maker could end up in a situation with varying pH of the entering pulp, which has a negative impact on paper quality and paper machine runnability.
  • NaHCO3 dissociates in the pulp suspension forming bicarbonate ions, HCO3 " , which have a buffering effect and therefore counteract any pH decrease.
  • NaHCO3 is a solid powder, which is generally supplied in so called big-bags, and the paper mill needs space for handling, equipment for dissolving and tanks for storage. The NaHCO3 is messy to work with, when in contact with moisture or water.
  • bicarbonate ions have been used to catalyze the reaction between the alkylketene dimers and the cellulose.
  • the bicarbonate ions may be generated by dissociation of carbon dioxide CO2 in the aqueous pulp.
  • Carbon dioxide is a gas, which easily dissolves under alkaline conditions, e.g. in water or a pulp suspension forming carbonic acid and/or bicarbonate ions according to the reaction:
  • Carbon dioxide has also been used for the pH control of pulp suspensions, for instance, in a process described in EP Patent 0 281 273, wherein gaseous carbon dioxide is introduced to adjust and maintain the pH at a value which is preferably between 7.0 and 5.5.
  • An object of the present invention is thus to provide a pH stabilization of aqueous pulp suspensions.
  • Another object of the invention is to provide a paper making pulp suspension having an increased alkalinity, i.e. a resistance to pH change.
  • a further object of the invention is to provide a technically advantageous process for buffering a pulp suspension.
  • An object is also to provide a pulp suspension having a controlled pH which is maintained at a desired level.
  • An object of the invention is also to provide a process for producing paper from a pulp suspension having a stabilized pH.
  • the present invention relates to a process for stabilizing the pH of a pulp suspension, wherein the alkalinity of a paper making pulp suspension is increased by adding thereto a combination of an alkali metal hydroxide feed and a carbon dioxide feed which feeds substantially counter each other's pH changing effect, said feeds being provided in an amount sufficient to achieve a significant buffering effect of said pulp suspension for paper making.
  • the feeding of a hydroxide and carbon dioxide in substantially countering amounts increases the level of alkalinity forming ions in the suspension without actually affecting its pH.
  • Increasing the alkalinity stabilizes the suspension against pH fluctuations caused by subsequent additions of acidic or basic fluids and provides a stable pH throughout the succeeding steps.
  • Alkalinity is a measurement of "acid resistance", i.e. the content of buffering ions in a liquid or pulp suspension, which counteracts pH decrease at addition of hydrogen ions, H + .
  • One way of expressing alkalinity is the amount of HCO3- and CO3 2 - ions in grams per liter.
  • the hydroxide used according to the invention should preferably be added prior to the addition of the carbon dioxide to ensure that the carbon dioxide is added under alkaline conditions.
  • the "amount sufficient to achieve a significant buffering effect” should be taken as meaning an amount providing a substantial and recognizable buffering effect in the pulp suspension.
  • the amount normally varies depending on the characteristics of the pulp and on the conditions of treatment. A person skilled in the art will be able to calculate the required amount based on his general knowledge or by simple tests made on the actual pulp suspension, as indicated, for example in Example 9 of this specification.
  • the amount of NaOH in the buffering combination will be between about 0.5 and 5 kg NaOH/ton dry cellulose and the amount of carbon dioxide in said combination will be between about 0.5 and 5 kg CO 2 /ton dry cellulose.
  • a typical buffering combination would include about 2 to 3 kg of NaOH and CO 2 per ton of dry cellulose. It is within the scope of the present invention to use more or less than the above mentioned amounts of both components, but in general it will be uneconomical to use more than what is required for a desired buffering action.
  • the buffering effect obtained by the addition of NaOH and CO 2 in this way corresponds to the one obtainable by an addition of dissolved NaHC ⁇ 3 but it has the advantage that the space consuming and messy handling of solid NaHCO3 is avoided.
  • Sodium hydroxide is a chemical which is abundantly available in the paper mill since it is used for many other purposes. Carbon dioxide gas may be generated on site or may be bought as desired. Feeding of carbon dioxide into the suspension is technically clean and easy.
  • a further advantage resides in that the hydroxide and carbon dioxide used according to the present invention may serve the dual purpose of increasing the alkalinity and of adjusting the pH.
  • the pH of said pulp suspension is increased by adding an excess of alkali metal hydroxide such as aqueous sodium hydroxide or decreased by adding an excess of carbon dioxide.
  • the carbon dioxide is preferably in gaseous form, although it may be added as an aqueous liquid by dissolving gaseous or solid carbon dioxide in water.
  • the hydroxide and carbon dioxide may be combined prior to feeding to the pulp suspension although it is preferred to feed them directly into the pulp circulation system such as to a pipe leading to a stock preparation tank.
  • the pulp suspension is preferably buffered by said combination to a pH between about 7 and 9.
  • the alkalinity of the pulp suspension is increased by providing a substantially equal molar amount of alkali metal hydroxide and dissolved carbon dioxide, said amount being sufficient to provide a significant buffering effect at about pH 8.
  • the pulp suspension may be bleached or unbleached chemical or mechanical pulp although the preferred pulp is bleached chemical pulp.
  • Calcium carbonate may advantageously be used as a filler for the pulp, since the stabilized pH will ascertain that the filler remains in solid form in the suspension. A fluctuation of the pH down to 6 or 5.5, for instance due to an inflow of circulating white water at such a pH, might dissolve the carbonate filler. Such an undesirable effect will be effectively prevented by the buffering action of the present invention.
  • the present invention also relates to a process for producing paper, said process comprising the steps of
  • bales of fully bleached kraft market pulp are introduced into a pulp slusher.
  • the pH in the slusher is adjusted with aqueous NaOH to a pH of approximately 11.
  • Example 1 The process of Example 1 is changed in order to improve the situation, so that a combination of NaOH and CO 2 is added to the pulp slusher.
  • the amount of NaOH added to the suspension is substantially increased compared to the process of Example 1.
  • a countering amount of CO 2 is added to provide a pH of approximately pH 9.
  • Example 3 After slushing, the same paper chemicals as in Example 1 are added to the slushed pulp suspension. Because of the buffering effect of the combined NaOH and CO 2 , the acidic additions lower the pH only to pH 7.2. This is a suitable pH for the short circulation and there is no need for any pH control using NaOH.
  • Example 3
  • a kraft pulp suspension having a pH of 5.1 is fed to a storage tower.
  • the pH of the pulp suspension Prior to the entry into the tower, the pH of the pulp suspension is adjusted to pH 8 by an addition of aqueous NaOH into the pipe leading to the tower.
  • the pulp suspension is fed from the storage tower to a refiner. At refining the pH decreases to about pH 6.
  • the low pH causes problems in the subsequent sizing of the pulp.
  • Example 3 The process of Example 3 is repeated with the exception that instead of feeding only the required amount of NaOH into the pulp suspension, an excess of NaOH is fed first into the pipe followed by feeding gaseous CO 2 into the pipe counteracting the excess NaOH.
  • the resulting suspension again has a pH of 8 when entering the storage tower.
  • 1 ml of the aqueous NaOH corresponds to about 2.5 kg/ton cellulose calculated on the dry weight basis; 1 g of CO similarly corresponds to about 2.5 kg/ton cellulose; and 1 ml of alum corresponds to about 2.8 kg/ton cellulose.
  • a pulp suspension was stored in a pulp storage tank in a pulp mill at a pH of 5.5 to 6.
  • the pulp was fed at this pH at a consistency of 3 to 4% to the paper mill via a press which increased the consistency to about 10% .
  • the pulp was fed at this consistency to the paper mill storage tank at a pH of 5.5 to 6.
  • White water from the paper machine was fed to the storage tank at a pH of 7.5 to 8.
  • the paper was produced with CaCO3 as filler. Some of the filler circulated with the white water to the storage tank. When entering the storage tank the CaC ⁇ 3 in the white water dissolved as it met the pulp suspension at pH 5.5 to 6.
  • the dissolving of the CaCO3 caused loss of filler and in addition thereto the calcium ions increased the hardness of the water and caused precipitations at unwanted positions.
  • Example 6 The process of Example 6 was repeated with the exception that aqueous NaHCO3 was fed to the paper mill storage tank to obtain the desired pH of about 7.5 to 8. The CaCO3 in the white water was not dissolved and the problem with filler loss was resolved.
  • the pH of the feed to the refiner was about 7.5 and no NaOH was fed to the suspension. However, in the refiner the pH decreased as before and a pH adjustment with NaOH was required for sizing.
  • Example 6 The process of Example 6 was repeated with the exception that NaOH and CO 2 were fed to the pipe leading to the paper mill storage tank. The pH was adjusted to 8 and no loss of filler occurred in the storage tank.
  • the pH of the feed to the refiner was about 8 and no NaOH was fed to the suspension. At refining the alkalinity of the suspension counteracted the pH lowering effect in a sufficient degree to retain the pH at 7.5 to 8.
  • a pulp suspension having a 10% consistency and a pH of 7.4 was divided into two lots, Pulp 1 and Pulp 2, respectively, weighing 2030 g each.
  • the pH of the pulp suspension was adjusted on one hand with sulfuric acid (a 10% by weight aqueous solution of H 2 SO4) and on the other hand with gaseous carbon dioxide and a combination of 1 M sodium hydroxide and carbon dioxide gas.
  • Pulp 1 The pH of Pulp 1 was adjusted to 6.2 with said sulfuric acid.
  • the pH of Pulp 2 was adjusted to 6.2 by adding 15 ml sodium hydroxide and 1,02 g of carbon dioxide.
  • the resulting pulp suspensions were titrated with 10% sulfuric acid to study their respective resistance to pH change. The results are indicated in Table 2 below.
  • the sulfuric acid in Table 2 is indicatied in kg of 100% H 2 SO4 per ton of dry cellulose.
  • NaOH was added in an amount of 2.9 kg/ ton cellulose and CO 2 was used in an amount of 5.1 kg/ ton cellulose.
  • the C0 2 was used both for pH adjustment and to counter the addition of sodium hydroxide.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Paper (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Detergent Compositions (AREA)
PCT/FI1998/000509 1997-06-13 1998-06-12 A PROCESS FOR STABILIZING THE pH OF A PULP SUSPENSION AND FOR PRODUCING PAPER FORM THE STABILIZED PULP Ceased WO1998056988A1 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
DE0991811T DE991811T1 (de) 1997-06-13 1998-06-12 VERFAHREN ZUR STABLISIERUNG DES pHS EINER ZELLSTOFFAUFSCHLÄMMUNG UND ZUR PAPIERHERSTELLUNG
EP98925673A EP0991811B1 (en) 1997-06-13 1998-06-12 A PROCESS FOR STABILIZING THE pH OF A PULP SUSPENSION AND FOR PRODUCING PAPER FORM THE STABILIZED PULP
AU77696/98A AU731377B2 (en) 1997-06-13 1998-06-12 A process for stabilizing the pH of a pulp suspension and for producing paper from the stabilized pulp
AT98925673T ATE204936T1 (de) 1997-06-13 1998-06-12 Verfahren zur stablisierung des phs einer zellstoffaufschlämmung und zur papierherstellung
JP50168899A JP2002504193A (ja) 1997-06-13 1998-06-12 パルプ懸濁液のpHを安定化するための及び安定化されたパルプから紙を製造するためのプロセス
CA002293405A CA2293405C (en) 1997-06-13 1998-06-12 A process for stabilizing the ph of a pulp suspension and for producing paper from the stabilized pulp
DE69801504T DE69801504T2 (de) 1997-06-13 1998-06-12 VERFAHREN ZUR STABLISIERUNG DES pHS EINER ZELLSTOFFAUFSCHLÄMMUNG UND ZUR PAPIERHERSTELLUNG
US09/445,710 US6991705B2 (en) 1997-06-13 1998-06-12 Process for stabilizing the PH of a pulp suspension and for producing paper from the stabilized pulp
NO19996070A NO328511B1 (no) 1997-06-13 1999-12-09 Fremgangsmate for a stabilisere pH i en pulpsuspensjon og fremstilling av papir av stabilisert pulp

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FI972522A FI102911B1 (fi) 1997-06-13 1997-06-13 Menetelmä massasuspension pH:n stabiloimiseksi ja paperin tuottamiseksi stabiloidusta massasta
FI972522 1997-06-13

Publications (1)

Publication Number Publication Date
WO1998056988A1 true WO1998056988A1 (en) 1998-12-17

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PCT/FI1998/000509 Ceased WO1998056988A1 (en) 1997-06-13 1998-06-12 A PROCESS FOR STABILIZING THE pH OF A PULP SUSPENSION AND FOR PRODUCING PAPER FORM THE STABILIZED PULP

Country Status (13)

Country Link
US (1) US6991705B2 (enExample)
EP (1) EP0991811B1 (enExample)
JP (1) JP2002504193A (enExample)
AT (1) ATE204936T1 (enExample)
AU (1) AU731377B2 (enExample)
CA (1) CA2293405C (enExample)
DE (2) DE69801504T2 (enExample)
ES (1) ES2161057T3 (enExample)
FI (1) FI102911B1 (enExample)
ID (1) ID29300A (enExample)
NO (1) NO328511B1 (enExample)
PT (1) PT991811E (enExample)
WO (1) WO1998056988A1 (enExample)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001075221A1 (en) * 2000-04-05 2001-10-11 Aga Ab A process for bleaching a lignocellulosic pulp
US6540870B1 (en) 1998-03-03 2003-04-01 Aga Aktiebolag Process for substantially retarding dissolution of calcium carbonate in a papermaking system
WO2003050356A1 (en) * 2001-12-12 2003-06-19 Linde Aktiengesellschaft An apparatus and a method for controlling the alkalinity and ph of an industrial process
US7056419B2 (en) 2002-09-30 2006-06-06 American Air Liquide, Inc. Methods for modifying electrical properties of papermaking compositions using carbon dioxide
EP1816259A1 (fr) * 2006-02-07 2007-08-08 L'AIR LIQUIDE, Société Anonyme pour l'Etude et l'Exploitation des Procédés Georges Claude Utilisation du dioxyde de carbone pour optimiser le pH dans la partie humide de la machine à papier
WO2008135631A1 (en) * 2007-05-04 2008-11-13 Kemira Oyj Method for preparing dithionite
WO2010023224A1 (en) * 2008-08-27 2010-03-04 Linde Aktiengesellschaft Process for preparing a buffer solution in a papermaking process
WO2011089176A1 (en) 2010-01-25 2011-07-28 Omya Development Ag Use of 2-((1-methylpropyl)amino)ethanol as additive in aqueous suspensions of calcium carbonate-comprising materials
WO2012101138A2 (de) 2011-01-25 2012-08-02 Basf Se Verfahren zur herstellung von halbstoffen für die produktion von papiererzeugnissen
WO2012101137A1 (de) 2011-01-25 2012-08-02 Basf Se Verfahren zur herstellung eines papiererzeugnisses
US10737302B2 (en) 2015-12-16 2020-08-11 Ecolab Usa Inc. Peroxyformic acid compositions for membrane filtration cleaning
US10834924B2 (en) 2014-12-18 2020-11-17 Ecolab Usa Inc. Generation of peroxyformic acid through polyhydric alcohol formate
US10899707B2 (en) 2014-12-18 2021-01-26 Ecolab Usa Inc. Methods for forming peroxyformic acid and uses thereof
US11026420B2 (en) 2016-12-15 2021-06-08 Ecolab Usa Inc. Peroxyformic acid compositions for membrane filtration cleaning in energy services
US11040902B2 (en) 2014-12-18 2021-06-22 Ecolab Usa Inc. Use of percarboxylic acids for scale prevention in treatment systems
US11241009B2 (en) 2016-04-15 2022-02-08 Ecolab Usa Inc. Performic acid biofilm prevention for industrial CO2 scrubbers
US11260040B2 (en) 2018-06-15 2022-03-01 Ecolab Usa Inc. On site generated performic acid compositions for teat treatment

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FI102911B1 (fi) * 1997-06-13 1999-03-15 Aga Ab Menetelmä massasuspension pH:n stabiloimiseksi ja paperin tuottamiseksi stabiloidusta massasta
SE514687C2 (sv) * 1999-07-09 2001-04-02 Sca Graphic Res Ab Metod för eliminering av skadliga substanser i en processvätska
US20040256069A1 (en) * 2003-06-18 2004-12-23 Saucedo Victor M. Estimation and control in the wet end using CO2
CA2643093C (en) * 2006-03-13 2010-11-30 Fpinnovations Near-neutral chlorine dioxide bleaching of pulp
FI20070126A0 (fi) * 2006-09-08 2007-02-13 Linde Ag Menetelmä hartsin poistamiseksi massasta ja hiilidioksidin tai (bi)karbonaatin käyttö tähän tarkoitukseen
US8034203B2 (en) * 2007-04-13 2011-10-11 United States Gypsum Company Gypsum wallboard with improved nail pull strength and the method for making same
FI120651B (fi) * 2007-04-30 2010-01-15 Linde Ag Menetelmä energiankulutuksen vähentämiseksi massasuspension jauhatuksessa paperinvalmistusprosessissa
FI20075503A7 (fi) * 2007-07-03 2008-06-19 Linde Ag Menetelmä paperin valmistamiseksi ja happo/emäskäsittelyn käyttö paperin valmistuksessa
FI122898B (fi) * 2009-01-14 2012-08-31 Linde Ag Menetelmä selluloosamassan pH:n säätämiseksi, sellun tai paperin valmistus selluloosamassasta ja (bi)karbonaattipoiston käyttö haponkulutuksen vähentämiseksi
DK2281853T3 (da) 2009-08-05 2012-07-23 Omya Development Ag Anvendelse af 2-amino-2-methyl-1-propanol som additiv i vandigesuspensioner af materialer, der indeholder calciumcarbonat
PL2363435T3 (pl) 2010-01-27 2012-04-30 Omya Int Ag Zastosowanie polietylenoimin jako dodatku w wodnych zawiesinach materiałów zawierających węglan wapnia
FI125826B (fi) * 2010-08-04 2016-02-29 Nordkalk Oy Ab Menetelmä paperin tai kartongin valmistamiseksi
PL2392622T3 (pl) 2010-06-07 2013-08-30 Omya Int Ag Zastosowanie 2-aminoetanolu jako dodatku w wodnych zawiesinach materiałów zawierających węglan wapnia
CN103492280B (zh) * 2011-04-20 2015-09-16 巴斯夫欧洲公司 纤维素防护包装材料
DK2824147T3 (en) 2013-07-12 2016-04-18 Omya Int Ag Use of 2-amino-2-ethyl-1,3-propanediol as an additive in aqueous suspensions of calcium carbonate comprising materials while maintaining stable suspension conductivity
SI3561002T1 (sl) 2018-04-23 2021-01-29 Omya International Ag Uporaba aditivov, ki vsebujejo primarne alkanolamine v vodnih mineralnih suspenzijah

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Cited By (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6540870B1 (en) 1998-03-03 2003-04-01 Aga Aktiebolag Process for substantially retarding dissolution of calcium carbonate in a papermaking system
US6623599B1 (en) 1998-03-03 2003-09-23 Aga Aktiebolag Process for producing a paper web having calcium carbonate filler by introducing carbon dioxide to the pulp
WO2001075221A1 (en) * 2000-04-05 2001-10-11 Aga Ab A process for bleaching a lignocellulosic pulp
NO337068B1 (no) * 2001-12-12 2016-01-11 Linde Ag Apparatur og fremgangsmåte for å regulere alkalinitet og pH i en industriell prosess
WO2003050356A1 (en) * 2001-12-12 2003-06-19 Linde Aktiengesellschaft An apparatus and a method for controlling the alkalinity and ph of an industrial process
US7175759B2 (en) 2001-12-12 2007-02-13 Linde Aktiengesellschaft Apparatus and a method for controlling the alkalinity and pH of an industrial process
CN1309906C (zh) * 2001-12-12 2007-04-11 兰德股份公司 控制工业过程的碱度和pH的装置和方法
AU2002350774B2 (en) * 2001-12-12 2008-03-13 Linde Aktiengesellschaft An apparatus and a method for controlling the alkalinity and pH of an industrial process
EP1953120A1 (en) 2001-12-12 2008-08-06 Linde Aktiengesellschaft An apparatus and a method for controlling the alkalinity and pH of an industrial process
US7056419B2 (en) 2002-09-30 2006-06-06 American Air Liquide, Inc. Methods for modifying electrical properties of papermaking compositions using carbon dioxide
EP1816259A1 (fr) * 2006-02-07 2007-08-08 L'AIR LIQUIDE, Société Anonyme pour l'Etude et l'Exploitation des Procédés Georges Claude Utilisation du dioxyde de carbone pour optimiser le pH dans la partie humide de la machine à papier
WO2008135631A1 (en) * 2007-05-04 2008-11-13 Kemira Oyj Method for preparing dithionite
US7993622B2 (en) 2007-05-04 2011-08-09 Kemira Oyj Method for preparing dithionite
WO2010023224A1 (en) * 2008-08-27 2010-03-04 Linde Aktiengesellschaft Process for preparing a buffer solution in a papermaking process
WO2011089176A1 (en) 2010-01-25 2011-07-28 Omya Development Ag Use of 2-((1-methylpropyl)amino)ethanol as additive in aqueous suspensions of calcium carbonate-comprising materials
EP2354191A1 (en) 2010-01-25 2011-08-10 Omya Development AG Use of 2-((1-methylpropyl)amino)ethanol as additive in aqueous suspensions of calcium carbonate-comprising materials
CN102712819A (zh) * 2010-01-25 2012-10-03 Omya发展股份公司 2-((1-甲基丙基)氨基)乙醇作为添加剂在包含碳酸钙的材料的含水悬浮液中的应用
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NO996070D0 (no) 1999-12-09
DE991811T1 (de) 2000-08-17
NO328511B1 (no) 2010-03-08
US20030150570A1 (en) 2003-08-14
CA2293405A1 (en) 1998-12-17
EP0991811B1 (en) 2001-08-29
EP0991811A1 (en) 2000-04-12
AU7769698A (en) 1998-12-30
ID29300A (id) 2001-08-16
ES2161057T3 (es) 2001-11-16
FI972522A0 (fi) 1997-06-13
NO996070L (no) 1999-12-09
PT991811E (pt) 2001-12-28
ATE204936T1 (de) 2001-09-15
DE69801504D1 (de) 2001-10-04
DE69801504T2 (de) 2002-04-25
JP2002504193A (ja) 2002-02-05
US6991705B2 (en) 2006-01-31
CA2293405C (en) 2006-08-08
FI102911B (fi) 1999-03-15
FI972522L (fi) 1998-12-14
FI102911B1 (fi) 1999-03-15
AU731377B2 (en) 2001-03-29

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