WO1995017546A1 - Inhibition of hydrogen peroxide decomposing enzymes, e.g. catalase and peroxidase during bleaching of cellulose fibers - Google Patents

Inhibition of hydrogen peroxide decomposing enzymes, e.g. catalase and peroxidase during bleaching of cellulose fibers Download PDF

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Publication number
WO1995017546A1
WO1995017546A1 PCT/SE1994/001245 SE9401245W WO9517546A1 WO 1995017546 A1 WO1995017546 A1 WO 1995017546A1 SE 9401245 W SE9401245 W SE 9401245W WO 9517546 A1 WO9517546 A1 WO 9517546A1
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Prior art keywords
hydrogen peroxide
bleaching
added
pulp
catalase
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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.)
Ceased
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PCT/SE1994/001245
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French (fr)
Inventor
Enn PÄÄRT
Kjell Abrahamsson
Peter Wållberg
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Bim Kemi AB
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Bim Kemi AB
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Publication date
Application filed by Bim Kemi AB filed Critical Bim Kemi AB
Priority to AT95905280T priority Critical patent/ATE190368T1/en
Priority to JP51736595A priority patent/JPH08507932A/en
Priority to US08/500,934 priority patent/US5885412A/en
Priority to EP95905280A priority patent/EP0686216B1/en
Priority to AU13949/95A priority patent/AU1394995A/en
Priority to DE69423344T priority patent/DE69423344T2/en
Publication of WO1995017546A1 publication Critical patent/WO1995017546A1/en
Priority to NO19953265A priority patent/NO318117B1/en
Priority to FI953933A priority patent/FI111966B/en
Anticipated expiration legal-status Critical
Ceased 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
    • D21C9/00After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
    • D21C9/10Bleaching ; Apparatus therefor
    • D21C9/1026Other features in bleaching processes
    • D21C9/1036Use of compounds accelerating or improving the efficiency of the 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
    • D21C5/00Other processes for obtaining cellulose, e.g. cooking cotton linters ; Processes characterised by the choice of cellulose-containing starting materials
    • D21C5/02Working-up waste paper
    • D21C5/022Chemicals therefor
    • 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
    • D21C9/00After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
    • D21C9/10Bleaching ; Apparatus therefor
    • D21C9/16Bleaching ; Apparatus therefor with per compounds
    • D21C9/163Bleaching ; Apparatus therefor with per compounds with peroxides
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/64Paper recycling

Definitions

  • Bacteria are often present when cellulose pulp is bleached, especially when recycled paper is used.
  • the bacteria produce enzymes like peroxidases and catalase that decompose hydrogen peroxide.
  • hydroxylamine salts in the presence of oxidizing agents (e.g. hydrogen peroxid under alkaline conditions. Therefore, the mention of hydroxylami and catalase inhibitors has to be regarded as pure speculation. Consequently, the use of hydroxylamine and catalase inhibitors i connection with bleaching of pulp with hydrogen peroxide cannot regarded as known in the art.
  • oxidizing agents e.g. hydrogen peroxid under alkaline conditions. Therefore, the mention of hydroxylami and catalase inhibitors has to be regarded as pure speculation. Consequently, the use of hydroxylamine and catalase inhibitors i connection with bleaching of pulp with hydrogen peroxide cannot regarded as known in the art.
  • hydroxylamine and its salts and addition salts e.g. hydroxylammonium sulfate and chloride
  • ascorbic acid e.g. ascorbic acid, and mixtures of these substances, mo preferably hydroxylammonium sulfate.
  • composition according to the invention can also contain 0.00 to 10 %(w/w) of one or more complexing agents to deactivate possible metal ions in the process, and 0.001 to 10 % (w/w) of surface active agents or detergents to enhance the distribution the inhibitor in the pulp.
  • Fig. 2 shows the result of the trial according to example 1.
  • the hydrogen peroxide concentration in the furnish from bleaching tower 6 is shown versus time.
  • the addition of the inhibitor started at time 0.
  • Example 1 Trial with hydroxylammonium sulfate as inhibitor in plant for treatment of recycled paper.
  • Hydroxylammonium sulfate has been tested as a catalase inhibito in a plant for treatment of recycled paper.
  • Fig 1 schematically shows how the recycled paper is treated in the plant.
  • a trial was run for 26 hours with addition of hydroxylammonium sulfate as a 10 % (w/w) solution.
  • T inhibitor solution was added before bleaching tower 6 into a mix (not shown) and in the microflotation.
  • the first dosage point wa chosen because the pulp before the mixer, in this system, has a low water content which gives a high concentration of inhibitor the pulp before adding the hydrogen peroxide in the bleaching tower 6.
  • the amount of added inhibitor was 1.9 kg/ton dry pulp a each dosing point during the whole trial.
  • Fig. 2 shows the concentration of hydrogen peroxide in mg/1 in t outlet from the bleaching tower 6 during the trial.
  • Example 2 Another experiment was carried out in the plant described in fig. 1.

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Paper (AREA)
  • Detergent Compositions (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Cosmetics (AREA)
  • Apparatus For Disinfection Or Sterilisation (AREA)

Abstract

The invention comprises a composition and use of said composition to suppress or inhibit the decomposing action of enzymes on hydrogen peroxide, e.g. peroxidase and catalase, during bleaching of cellulose fibres with hydrogen peroxide, especially in connection with the production of recycled paper, in such a way that microorganisms are not markedly affected, and discharges that are dangerous to the environment are minimized. The composition contains hydroxylamine, thiocyanate salts, formic acid, ascorbic acid or nitrites. The invention also comprises a method for treatment and bleaching of cellulose.

Description

INHIBITION OF HYDROGEN PEROXIDE DECOMPOSING ENZYMES. E.G. CATALASE AND PEROXIDASEDURINGBLEACHINGOFCELLULOSEFIBERS
The present invention relates to the use of substances that inhibit or degrade enzymes when bleaching fibres of cellulose wi hydrogen peroxide, a method for treating and bleaching cellulose pulp and a composition containing the substances.
A criterion of paper quality is that it has high brightness and consequently is made from a sufficiently bleached pulp-
Different methods are known for bleaching of cellulose pulp such as addition of chlorine, hypochlorite, oxygen, ozone or hydrogen peroxide. These methods are generally combined in a bleaching process. Lately, environmental problems have attracted more attention and attempts have therefore been made to avoid bleachi with chlorine containing compounds since these, even in small quantities, are considered dangerous to the environment, despite satisfactory bleaching with these chemicals. Oxygen containing compounds such as hydrogen peroxide, oxygen and ozone have therefore found increased use for bleaching of pulp. These compounds are decomposed to oxygen or substances that are environmentally acceptable. Hydrogen peroxide is preferred over ozone for economic and environmental reasons.
Bacteria are often present when cellulose pulp is bleached, especially when recycled paper is used. The bacteria produce enzymes like peroxidases and catalase that decompose hydrogen peroxide.
Attempts have been made to overcome the degrading action of the enzymes, especially catalase, by overdosing hydrogen peroxide, sometimes 6-8 times the normal dosage. Overdosing the hydrogen peroxide leads to a high dosage of sodium hydroxide and sodium silicate, and accordingly to increased costs.
Inhibition of catalase by can also be accomplished by raising th temperature to 60-90°C or the pH to 10-14. However, a temperatur rise may lead to a faster decomposition of the hydrogen peroxide and increased pH leads to yellowing of the pulp and consequentl need for more intense bleaching or a degradation of the pulp.
It has also been suggested that biocides could be added to kill the microorganisms and prevent the formation of catalase. Bioci are dangerous to the health and unsuitable from an environmental point of view. Moreover, when the microorganisms die, more catalase can come out into the process water.
Metal ions that are present, for example iron, manganese, copper and aluminium ions decompose hydrogen peroxide. To prevent this, complexing agents and sodium silicate are used today. Silicates are inclined to form deposits and the complexing agents are expensive and sometimes dangerous to use. Their influence on the environment is strongly questioned and not completely investigated.
By EP 0 562 835, it is known that small amounts of chlorine dioxide, bromine, chlorine, iodine and ozone can be used as oxidizing, enzyme inhibiting and ger icidal agents when bleachin cellulose pulp with hydrogen peroxide. According to example 3 in the description, microorganisms in white water are killed with chlorine dioxide. Chlorine dioxide is a poisonous, explosive, corrosive and awkward substance that easily decomposes and has t be produced on site and kept in a dilute water solution. From an environmental point of view, these kinds of additives are also highly questioned.
US-A-3 817 828 describes a method in which anionic surface activ agents are combined with bacteriecidal substances, e.g. chlorine dioxide, hypochlorite or chlorine water to prevent bacterial growth. The used chlorine compounds are poisonous and dangerous the environment, and although the method is declared to decrease the use of these, some chlorine compounds will be released to th environment.
G. Galland, E. Bernard, Y. Verac suggest in "Achieving a deinked pulp with high brightness " in Paper Technology, dec. 1989 different ways to increase the brightness when processing recycl paper by decreasing the hydrogen peroxide consumption. For instance, it is suggested that catalase are removed by eliminat the microorganisms that produce the enzyme or by destroying catalase before bleaching. A sodium hypochlorite treatment may used to destroy catalase. However, sodium hypochlorite is a substance that is unsuitable for environmental reasons.
In principle the methods given in the two publications involve use of bleaching agents that are harmful to the environment and are avoided nowadays, in small amounts in order to kill the microorganisms and deactivate the enzyme.
Additions of substances that affect the bleaching with hydrogen peroxide have been suggested. US-A 3 193 445 describes a method which the addition of 0,5 to 2,5 moles of acetic anhydride per mole remaining hydrogen peroxide is added in the end of the bleaching process in order to activate the remaining peroxide.
Accordingly, the bleaching process of the pulp is prolonged.
Derwent's abstract of SU 796 281 describes a method where 0.1 - (w/w%) oxalate (calculated on dry pulp basis) is added together with hydrogen peroxide under alkaline conditions at 60-70°C.
However, none of these references mention anything about the possibility to intensify the action of hydrogen peroxide by inhibiting hydrogen peroxide decomposing enzymes like peroxidas and catalaseε.
According to the present invention, the use of one or more substances is suggested, that suppress or inhibit the degrading effect of enzymes, such as peroxidases and catalases, decomposi hydrogen peroxide during bleaching of cellulose fibres with hydrogen peroxide, and which substances do not affect micro¬ organisms.
Preferred substances are those that are not harmful to the environment and therefore can be handled without special considerations when used in the bleaching process and then let into the sewer without affecting a possible following biologica purifying plant, before the water is released to the environmen Substances which are not or will not form halogen containing compounds that are dangerous to the environment are preferred. These substances do not affect modern biocide free slime control methods (Biochem®, Bimogard®) that are used to an increasing extent in the cellulose- and pulp industry. In contrast to biocides, they are expected to have a advantageous effect on thi kind of process.
Hydrogen peroxide can enter the cells of microorganisms and be degraded internally by peroxide decomposing enzymes, especially catalase. The decomposition also takes place outside the cells because such enzymes are secreted. The amount of catalase is increased if the cells are killed and disrupted. Therefore, it i assumed that the optimal inhibition of the decomposing effect of catalase occurs when the catalase outside the cells is deactivat without killing and disrupting the microorganisms.
GB-A-2 269 191 that was published after the priority date of the present application, deals with a method of bleaching with hydrogen peroxide, where an organic peracid is added as a biocid to kill and prevent growth of catalase producing microorganisms. It is incidentally stated that it is known that catalase inhibitors like hydroxylamine are used in connection with pulp bleaching using hydrogen peroxide. However, no references to kno techniques are given, and the document does not account for experiments where catalase is inhibited. In safety data sheets from manufacturers (Raschig, BASF) of hydroxylamine and hydroxylamine salts, it is announced that hydroxylamine is decomposed in aqueous solution if hydrogen peroxide is present. Moreover, a warning is issued against the use of hydroxylamine salts in the presence of oxidizing agents (e.g. hydrogen peroxid under alkaline conditions. Therefore, the mention of hydroxylami and catalase inhibitors has to be regarded as pure speculation. Consequently, the use of hydroxylamine and catalase inhibitors i connection with bleaching of pulp with hydrogen peroxide cannot regarded as known in the art.
It is assumed, without limiting the invention to this theory, th the inhibiting effect of the substances arises from blocking or destroying the active sites on the enzyme molecule. The active site of catalase contains iron or manganese ions that can be blocked or deactivated by complex formation. The substances can also inhibit other enzymes than catalase, e.g. peroxidases.
The following substances can be used according to the invention:
Hydroxylamine and alkyl derivatives having 1 - 10 carbon atoms i a straight or branched chain such as, for example, methylhydroxylamine, and their salts and addition salts such as hydroxylammonium sulfate and -chloride; thiocyanates such as ammonium thiocyanate; formic acid, ascorbic acid, salicylic acid nitrites such as sodium nitrite, potassium nitrite, calcium nitrite and magnesium nitrite. These substances can also be mixe As mentioned earlier, halogen containing substances that are dangerous to the environment are avoided. Certain halogen salts may however be environmentally harmless at the used concentrations.
Preferably the following substances are used; hydroxylamine and its salts and addition salts, e.g. hydroxylammonium sulfate and chloride; ascorbic acid and and mixtures of these substances, mo preferably hydroxylammonium sulfate.
The enzyme inhibitors according to the invention can be used for bleaching all kinds of cellulose pulps, especially pulp made fro recyclable paper, but also pulps from sulfite or sulfate cooking mechanical pulp, thermomechanical pulp and chemothermomechanical pulp. As the catalase inhibiting substances according to the invention do not affect the microorganisms, they can also be suitable for bleaching with hydrogen peroxide of pulps that have been produced by microbiological lignin degradation.
The invention also comprises an enzyme inhibiting composition th is characterized by containing at least one catalase inhibiting substance according to the invention. These compositions can consist of the catalase inhibiting substance per se, or mixtures containing the substance in a solid or liquid form or a solution or suspension of the substance (substances) . As solvent or suspending agent, water or an organic solvent may be used that i consistent with the intended purpose and does not affect the bleaching or the treatment of the cellulose pulp in a negative way. The composition can contain 0.1 -100 % (w/w) of the catalas inhibiting substance, particularly 1 - 50 %, especially 5-20 %, and most preferably 10%. Water solutions are preferred.
The composition according to the invention can also contain 0.00 to 10 %(w/w) of one or more complexing agents to deactivate possible metal ions in the process, and 0.001 to 10 % (w/w) of surface active agents or detergents to enhance the distribution the inhibitor in the pulp.
Suitable complexing agents include e.g. phosphonic acids, aminopolycarbonic acids like EDTA, EGTA and DTPA and various aci like gluconic acid, tartaric acid and citric acid.
Suitable detergents can be anionic, cationic, nonionic or amphoteric, and include the following:
1: Salts of carboxylic acids of the type RCOOM where R is a carb chain having 9 - 21 carbon atoms and M is an alkali metal.
2: Quaternary ammonium salts
3: Alcohol ethoxylates 4: Alkylbetaines
The components of the composition have, as mentioned earlier, lo toxicity for microorganisms. Table 1 shows EC20 -data for standar chemicals used in the pulp and paper industry together with components of the inhibiting composition.
The invention also includes a method for treatment and hydrogen peroxide bleaching of cellulose, where at least one substance according to the invention is added.
The enzyme inhibiting substance or composition according to the invention can be added anywhere in the pulp bleaching process. Consequently, it is possible to add the composition or the substances anywhere in the treatment of the cellulose pulp such at the production of the pulp itself before the bleaching step.
The invention especially comprises a method for bleaching recycl paper, where paper, water, chemicals, such as alkali silicates, surface active agents, such as tensides, and possibly complexing agents are suspended. The suspension is purified and dewatered, the pulp is bleached with hydrogen peroxide and deinked by flotation or washing, possibly also with cyclones, vortex cleaners, screening and filtering, which method is characterized by the addition of at least one catalase inhibitor before bleaching, and optionally to the white water coming from the various process stages and preferably by the presence of hydroge peroxide in the flotation stage.
The hydrogen peroxide and/or the inhibitor are preferably added one or more of the following stages in the process: the mixing screw before the bleaching tower, at the flotation, at the pulpe in the incoming white water from the press and in the white wate tanks. Most preferably, hydrogen peroxide is added in the pulper and/or the bleaching tower. It is especially preferred to add th catalase- or peroxidase inhibitor at the suction side of the pum in the white water system, directly into the white water tanks, the water from the paper machines and in the purified water from the micro flotation.
White water in this context means a separated liquid that is recirculated to a preceding stage, especially to the first disintegration stage, where paper, water and chemicals are mixed
Bleaching with hydrogen peroxide is usually carried out at pH greater than 7 and the pH is generally more than 5, preferably over 8, for example between 7 and 12, most preferably between 8 and 11.5.
The necessary amount of inhibitor can be determined by someone skilled in the art after determination of the remaining hydrogen peroxide in the process water and pulp and with regard to the brightness of the pulp. The brightness depends on the pH, temperature, to what extent the process water is recirculated an the used pulp, especially when recycled paper is used, because pulp can contain varying amounts of microorganisms depending on the conditions under which it is stored. The added amount of enzyme inhibiting substance is generally 0.001 - 1.5 % (w/w), calculated on dry pulp basis, preferably 0.01 - 0.5 %, most preferably 0.01 - 0.05 %. Sometimes considerably larger amounts may be needed.
Alternatively, the addition can be done with 0.5 - 110 % (w/w), preferably 5 -50 % enzyme inhibiting substance calculated on ad hydrogen peroxide basis. The larger amounts are added when the hydrogen peroxide concentration has decreased.
The invention will now be described in detail with reference to the enclosed figures.
Fig. 1 shows a block diagram of a bleaching process using recycl paper. In a pulper 1 recycled paper, water, sodium hydroxide, hydrogen peroxide and a collector (Raisapon,dispersion of fatty acids) are added. The fibre suspension is cleaned and dewatered through the coarse screener 2 , turbo separator 3, and reject screening cyclones 4. After the belt press 5 , complexing agents (e.g. a magnesium complex with DTPA) together with hydrogen peroxide and sodium hydroxide are added and the pulp is sent to the bleaching tower 6 by means of mixing screw (not shown) , cleaned in sand vortex cleaners 7, flotated in the primary and secondary flotation cells 8 and 9, and passed through vortex cleaners 10 and 12 , fine screening 11, disc filters 13, screw presses 14, kneeders (Frota pulpers) 15, and finally, it is sent to storage tower 16 before the paper machine.
A part of the separated water from the belt presses 5 goes to th micro flotation unit 17 and forms white water I that is returned to pulper 1 via white water tank 18. Separated material from the micro flotation unit 17 goes to the centrifuge 19 after the secondary flotation unit 9, and the liquid from centrifuge 19 is returned to the icroflotation unit 17.
Liquid from disc filters 13 goes to white water tank 20, where also drainage water from the press section 21 in the paper machi is added. From the white water tank 20, white water II is broug to white water tank 18 and further to pulper 1.
Fig. 2 shows the result of the trial according to example 1. The hydrogen peroxide concentration in the furnish from bleaching tower 6 is shown versus time. The addition of the inhibitor started at time 0.
Fig. 3 shows the result from the trial in example 2. The hydroge peroxide concentration in the process water from white water tan 18 is given vs time. The inhibiting substance was added solely i the water from the presses 21 during the first 55 hours. After that, the addition was done both in press water 21 and white wat I between the microflotation 17 and white water tank 18.
Fig. 4 shows the decomposition of the hydrogen peroxide in the white water at the start of the trial (graph A) and the end of t trial according to example 2. (graph B)
Fig. 5 shows decomposition of added hydrogen peroxide when testi catalase containing water from the micro flotation 17 in fig.l a normal operation without inhibitor (graph H) and with addition o 1 mmol/1 (graph G) hydroxylammonium chloride.
Fig. 6 shows graphs similar to fig. 4 but without addition of inhibitor (graph Q) , 1 mmol/1 hydroxylammonium chloride (graph O and 0.5 mmol/1 each of hydroxylammonium chloride and ascorbic ac (graph P) .
Fig. 7 shows the inhibiting effect of hydroxylammonium sulfate (graph A) , ammonium thiocyanate (graph B) and formic acid (graph compared to iodine (graph D) and with catalase solution prepared in the laboratory in the presence of hydrogen peroxide.
Practical examples are given below to illustrate the invention without thereby restricting its scope. The given weights are bas on dry pulp. Example 1 Trial with hydroxylammonium sulfate as inhibitor in plant for treatment of recycled paper.
Hydroxylammonium sulfate has been tested as a catalase inhibito in a plant for treatment of recycled paper. Fig 1 schematically shows how the recycled paper is treated in the plant.
In a plant according to fig 1, a trial was run for 26 hours with addition of hydroxylammonium sulfate as a 10 % (w/w) solution. T inhibitor solution was added before bleaching tower 6 into a mix (not shown) and in the microflotation. The first dosage point wa chosen because the pulp before the mixer, in this system, has a low water content which gives a high concentration of inhibitor the pulp before adding the hydrogen peroxide in the bleaching tower 6. The amount of added inhibitor was 1.9 kg/ton dry pulp a each dosing point during the whole trial.
In the beginning of the trial, the added hydrogen peroxide was 1 kg (50 % (w/w) ) /ton dry pulp (5 kg/ton in the pulper and 10 kg/ton in the mixing screw before the bleaching tower 6) .
The concentration of hydrogen peroxide was determined by the method described by Vogel, Artur I.: Vogel's textbook of quantitative chemical analysis, 5th edition, page 394.
Fig. 2 shows the concentration of hydrogen peroxide in mg/1 in t outlet from the bleaching tower 6 during the trial.
The trial was run so that the brightness levels was the same as usual.
Example 2 Another experiment was carried out in the plant described in fig. 1.
The experiment lasted 132 hours and 14 kg hydrogen peroxide (50 (w/w) ) per ton dry pulp was added. A water solution of hydroxylammonium sulfate (10 %(w/w)) was first added solely to t white water coming from the paper machine 21. The added amount w 1.4 kg per ton dry pulp. This, however, gave a low hydrogen peroxide concentration. After 55 hours the addition was increas to 1.4 kg/ton in the white water and 1.7 kg/ton to the microflotation. This resulted in a strong increase in the hydro peroxide concentration in the white water and consequently, it possible to decrease the addition of hydrogen peroxide with thi inhibitor dosage.
Fig. 3 shows how the concentration of hydrogen peroxide varied during the trial
Fig. 4 shows the decomposition of the hydrogen peroxide at the beginning of the trial (graph A) and at the end (graph B) .
Example 3 Catalase inhibiting effects of hydroxylammonium chloride.
In another experiment, hydroxylammonium chloride was added to a sample of process water from the micro flotation unit 17 in the plant according to fig. 1, to the final concentration 1 mmol/1. The production was run without any inhibitor according to the invention and the addition of hydrogen peroxide was done in the same way as in example 1. Fig. 5 shows the percentage of remain hydrogen peroxide as a function of time after the addition of hydroxylammonium chloride. Graph G shows the concentration of remaining hydrogen peroxide when hydroxylammonium chloride was added and graph H without any addition.
One hour after the addition of hydroxylammonium chloride, approximately 75 % of the hydrogen peroxide remained.
Example 4 Catalase inhibiting effect of hydroxylammonium chlori and ascorbic acid.
To examine the combined effects of hydroxylammonium chloride an ascorbic acid, 0.05 mmol of each were added to catalase containi v~'ter from the screw presses, and in a second experiment 1 _,droxylammonium chloride (1 m ol/ 1) only. Fig. 6 shows remaini hydrogen peroxide when two inhibitors were added (graph P) , only hydroxylammonium chloride (graph O) and without inhibitor (graph Q) .
Example 5 Analysis of the inhibition of catalase by formic acid hydroxylammonium sulfate, ammonium thiocyanate and in a buffered solution of hydrogen peroxide (0.1 w/w%) at pH 7.
The catalase inhibiting effect of some substances were examined a buffered solution of hydrogen peroxide at pH 7.
A buffer solution was prepared by dissolving KH2P04 and Na2HP04 a final concentration of 0.025 M each. Five mg of catalase was dissolved in 100 ml of the buffer solution. The catalase was supplied by Sigma and had an activity of 2000 units per mg protein. One unit will decompose 1 μmole hydrogen peroxide per minute at pH 7 and 25°C, which leads to a fall in hydrogen peroxide concentration from 10.3 to 9.2 mM.
20 ml of the buffered catalase solution and 1 mmol inhibitor wer mixed with 180 ml buffer solution and 2 ml 10 % (w/w) hydrogen peroxide was added. Hydroxylammonium sulfate, ammonium thiocyana and formic acid were tested.
Remaining hydrogen peroxide was determined in 50 ml samples afte
5 and 15 minutes.
Fig. 7 shows remaining hydrogen peroxide in percent after additi of hydroxylammonium sulfate (graph A) , ammonium thiocyanate (gra
B) and formic acid (graph C) .
It is evident that these inhibitors are more effective than iodi (graph D) according to EP 0 562 835. Table 1
Product Concentration (%) EC20 (mg/1) Dosage (mg
Neutral size 12 1780 100
Defoamer 30 104 1
Resin size 30 6.9 100
Hydrogen peroxide 35 24 100
Peracetic acid 11 0.49 100
Glutaraldehyde 50 2.6 100 Hydroxylammonium sulfate 10 550 150
These toxicity tests was made with a Microtox™-kit (Bio Orbit, Turku, Finland) according to the manufacturer's directions. A h EC20-value means low toxicity.

Claims

Claims
1. A composition for inhibiting hydrogen peroxide decomposing enzymes, such as peroxidases and catalases", containing at least one inhibiting substance, such as hydroxylamine and its alkyl derivatives having 1 - 10 carbon atoms in a straight or branched chain such as, for example, methyl hydroxyl amine, and their and salts and addition salts, such as hydroxylammonium sulfate or hydroxylammonium chloride, thiocyanate salts such as ammonium thiocyanate, formic acid, ascorbic acid, and nitrites such as sodium nitrite, potassium nitrite, magnesium nitrite or calcium nitrite.
2. A composition according to Claim 1, characterized in that the composition also contains one or more complexing agents and/or o or more detergents.
3. A composition according to Claim 1 or 2, characterized in tha the composition contains hydroxylamine, hydroxylammonium sulfate or hydroxylammonium chloride.
4. Use of a composition according to anyone of Claims 1 -3 for treating and/or bleaching cellulose with hydrogen peroxide.
5. Use according to Claim 4, where the cellulose is a cellulose pulp, made from recycled paper.
6. A method for treating and/or bleaching of cellulose with hydrogen peroxide, characterized in that a composition according to anyone of Claims 1 - 3 is added in such amounts that will cau inhibition of peroxidases and/or catalases and that will not significantly affect the microorganisms.
7. A method according to Claim 6 characterized in that the added amount of enzyme inhibiting substance is 0.001 - 1.5 % (w/w) calculated on dry pulp, and preferably 0.01- 0.5 %.
8. A method according to Claim 6, characterized in that 0.5 - 11 (w/w) , preferably 5 - 50 % enzyme inhibiting substance, calculat on the added hydrogen peroxide, is added.
9. A method according to anyone of Claims 6 - 8, characterized i that cellulose pulp is produced and bleached, and that the enzym inhibiting substance is added anywhere during the pulp productio or bleaching, preferably before the bleaching and possibly to process water recirculated for bleaching.
10. A method according to anyone of Claims 6 - 9, characterized that the enzyme inhibiting substance is added to enhance the flotation of impurities.
PCT/SE1994/001245 1993-12-23 1994-12-22 Inhibition of hydrogen peroxide decomposing enzymes, e.g. catalase and peroxidase during bleaching of cellulose fibers Ceased WO1995017546A1 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
AT95905280T ATE190368T1 (en) 1993-12-23 1994-12-22 INHIBITION OF HYDROGEN PEROXIDE DEGRADING ENZYMES, E.G. CATALASE AND PEROXIDASE, IN BLEACHING CELLULOSIC FIBERS
JP51736595A JPH08507932A (en) 1993-12-23 1994-12-22 How to bleach cellulose
US08/500,934 US5885412A (en) 1993-12-23 1994-12-22 Inhibition of hydrogen peroxide decomposing enzymes during bleaching of cellulose fibers
EP95905280A EP0686216B1 (en) 1993-12-23 1994-12-22 Inhibition of hydrogen peroxide decomposing enzymes, e.g. catalase and peroxidase during bleaching of cellulose fibers
AU13949/95A AU1394995A (en) 1993-12-23 1994-12-22 Inhibition of hydrogen peroxide decomposing enzymes, e.g. catalase and peroxidase during bleaching of cellulose fibers
DE69423344T DE69423344T2 (en) 1993-12-23 1994-12-22 INHIBITION OF HYDROGEN PEROXIDE-DEGRADING ENZYMES, e.g. CATALASE AND PEROXIDASE, WHEN BLEACHING CELLULOSIC FIBERS
NO19953265A NO318117B1 (en) 1993-12-23 1995-08-18 Use of a composition to inhibit hydrogen peroxide-forming enzymes, e.g. catalase and peroxidase by bleaching cellulose fibers
FI953933A FI111966B (en) 1993-12-23 1995-08-22 Inhibition of hydrogen peroxide decomposing enzymes, e.g. catalase and peroxidase in bleaching cellulose fibers

Applications Claiming Priority (2)

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SE9304277A SE505980C2 (en) 1993-12-23 1993-12-23 Ways to prevent peroxide-degrading enzymes by bleaching with hydrogen peroxide
SE9304277-8 1993-12-23

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WO1995017546A1 true WO1995017546A1 (en) 1995-06-29

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DE (1) DE69423344T2 (en)
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NO (1) NO318117B1 (en)
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2390408A1 (en) 2010-05-31 2011-11-30 Kemira Oyj Control of enzymes in the production of pulp

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6355179B1 (en) 1999-12-10 2002-03-12 Basf Corporation Decomposition of residual hydroxylamine by hydrogen peroxide treatment
GB0001417D0 (en) * 2000-01-22 2000-03-08 Albright & Wilson Uk Ltd Bleaching pulp
EP1294980B2 (en) 2000-06-08 2015-10-07 Lonza Inc. Aldehyde donors for stabilizing peroxides in papermaking applications
DE10126988A1 (en) * 2001-06-05 2002-12-12 Call Krimhild Systems for oxidation or bleaching, especially of pulp, comprise a component enzymatically generating peroxide, superoxide or other reactive oxygen species, and a precursor formed enzymatically, or is oxidizably reactive
US7052614B2 (en) * 2001-08-06 2006-05-30 A.Y. Laboratories Ltd. Control of development of biofilms in industrial process water
US20040200588A1 (en) * 2003-04-10 2004-10-14 Walker Jayne M.A. Method of controlling microorganisms in hydrogen peroxide pulp bleaching processes
JP5122821B2 (en) 2003-11-28 2013-01-16 イーストマン ケミカル カンパニー Cellulose interpolymer and oxidation method
US7297225B2 (en) 2004-06-22 2007-11-20 Georgia-Pacific Consumer Products Lp Process for high temperature peroxide bleaching of pulp with cool discharge
GB0421359D0 (en) * 2004-09-24 2004-10-27 Basf Ag Method for the inactivation of enzymes
US8138106B2 (en) 2005-09-30 2012-03-20 Rayonier Trs Holdings Inc. Cellulosic fibers with odor control characteristics
US20090208543A1 (en) * 2008-01-22 2009-08-20 Oral Health Clinical Services Method and apparatus for applying a protective oral care composition
JP5364442B2 (en) * 2008-05-19 2013-12-11 ライオン株式会社 Bleaching aid composition and pulp bleaching method
AU2009316659B2 (en) * 2008-11-21 2013-06-27 Buckman Laboratories International, Inc. Method for controlling enzymatic decomposition of peroxide and products thereof
GB0901207D0 (en) * 2009-01-26 2009-03-11 Innospec Ltd Chelating agents and methods relating thereto
JP2010236166A (en) * 2009-03-31 2010-10-21 Nippon Paper Industries Co Ltd Method for producing deinked pulp
WO2013188497A2 (en) * 2012-06-15 2013-12-19 Agentase, Llc, A Subsidiary Of Flir Systems, Inc. A smart, self-decontaminating polymer and method for inhibiting the growth of a bacteria and fungus

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3193445A (en) * 1962-07-16 1965-07-06 Pittsburgh Plate Glass Co Method of bleaching cellulosic materials with hydrogen peroxide
EP0562835A1 (en) * 1992-03-24 1993-09-29 ALBRIGHT & WILSON UK LIMITED Stabilisation of bleach liquors
GB2269191A (en) * 1992-07-29 1994-02-02 Solvay Interox Ltd Method of treating aqueous process liquors

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2838459A (en) * 1955-02-01 1958-06-10 Pennsalt Chemicals Corp Stabilization of solutions containing peroxygen compounds
GB846079A (en) * 1958-07-11 1960-08-24 Canadian Ind Improvements in and relating to manufacture of unbleached and semi-bleached sulphite pulp
US3606990A (en) * 1970-02-12 1971-09-21 Colgate Palmolive Co Process for washing laundry and detergent composition for working of this process
US3817828A (en) * 1970-09-30 1974-06-18 B Bendiner Method of microbiological control of paper mill processes
US3751222A (en) * 1971-12-13 1973-08-07 Colgate Palmolive Co A process of cleaning cloth
SU796281A1 (en) * 1979-03-27 1981-01-15 Институт Физико-Органической Хи-Мии Ah Белорусской Ccp Wood pulp bleaching method
DE3531563A1 (en) * 1985-09-04 1987-03-05 Benckiser Knapsack Gmbh WOOD FABRICS
DE3636208A1 (en) * 1986-10-24 1988-05-05 Call Hans Peter METHOD FOR DELIGNIFYING AND WHICH BLEACHING LIGNICELLULOSE-CONTAINING OR LIGNINAL MATERIAL OR LIGNIN BY ENZYMATIC TREATMENT
SE8700569D0 (en) * 1987-02-12 1987-02-12 Josef Kubat AN IMPROVED PEROXIDE BLEACHING METHOD
US4871423A (en) * 1987-08-10 1989-10-03 Hoechst Celanese Corporation Enhanced dithionite bleaching
DE4137761A1 (en) * 1991-05-17 1992-11-19 Call Hans Peter METHOD FOR DELIGNIFYING LIGNOCELLULOSE-CONTAINING MATERIAL, BLEACHING AND TREATING WASTEWATER BY LACCASE WITH EXTENDED EFFECTIVENESS
DE69309662D1 (en) * 1992-01-31 1997-05-15 Actimed Lab Inc INHIBITION OF CATALASE ACTIVITY IN BIOLOGICAL LIQUIDS
ES2147579T3 (en) * 1993-06-16 2000-09-16 Call Hans Peter BLEACHING SYSTEM OF MULTIPLE COMPONENTS.

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3193445A (en) * 1962-07-16 1965-07-06 Pittsburgh Plate Glass Co Method of bleaching cellulosic materials with hydrogen peroxide
EP0562835A1 (en) * 1992-03-24 1993-09-29 ALBRIGHT & WILSON UK LIMITED Stabilisation of bleach liquors
GB2269191A (en) * 1992-07-29 1994-02-02 Solvay Interox Ltd Method of treating aqueous process liquors

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Advances in Enzymology, Volume, No. 3, 1943, KJELL AGNER, "Verdoperoxidase", page 137 - page 148, see page 145. *
DERWENT'S ABSTRACT, No. 75145 D/41, week 8141; & SU,A,796281 (AS BELO PHYS ORGAN), 15 January 1981 (15.01.81). *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2390408A1 (en) 2010-05-31 2011-11-30 Kemira Oyj Control of enzymes in the production of pulp
WO2011151260A1 (en) 2010-05-31 2011-12-08 Kemira Oyj Control of enzymes in the production of pulp

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AU1394995A (en) 1995-07-10
DE69423344D1 (en) 2000-04-13
FI111966B (en) 2003-10-15
CA2155124A1 (en) 1995-06-29
FI953933A0 (en) 1995-08-22
DE69423344T2 (en) 2000-07-27
ATE190368T1 (en) 2000-03-15
US5885412A (en) 1999-03-23
SE9304277L (en) 1995-06-24
SE9304277D0 (en) 1993-12-23
EP0686216B1 (en) 2000-03-08
NO953265L (en) 1995-08-18
CA2155124C (en) 1998-08-04
JPH08507932A (en) 1996-08-27
NO953265D0 (en) 1995-08-18
NO318117B1 (en) 2005-02-07
SE505980C2 (en) 1997-10-27
EP0686216A1 (en) 1995-12-13
FI953933L (en) 1995-08-22

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