Ozone bleaching of low consistency pulp

Information

  • Patent Grant
  • 6793771
  • Patent Number
    6,793,771
  • Date Filed
    Monday, June 16, 2003
    21 years ago
  • Date Issued
    Tuesday, September 21, 2004
    19 years ago
Abstract
Provided is a process for bleaching pulp with ozone. The process involves preparing a slurry of cellulosic pulp having a consistency in fibers of from 1-5 weight %. Such a low consistency slurry is then mixed with ozone under high shear conditions. The ozone is then maintained in contact with the cellulosic fibers to effect bleaching of the fibers. The present process offers the advantages of bleaching using a low consistency slurry, with the added advantages of employing ozone.
Description




BACKGROUND OF THE INVENTION




1. Field of the Invention




The present invention relates to a method for bleaching pulp. More specifically, the present invention relates to a method of bleaching pulp using ozone in which the ozone is more effectively dispersed and dissolved in a low consistency pulp.




2. Brief Description of the Prior Art




During the past 10-15 years the bleaching of pulp in the Kraft Process has undergone many changes. These changes were mainly prompted by environmental concerns of the quality of the effluent being discharged from paper mills. Of main concern was the bleach plant effluent, which contained polychlorinated dibenzodioxines and dibenzofurans among other compounds. The measurement of AOX was used as an indicator of the concentration of these compounds and the test was quickly adopted as a standard for legislation.




It was soon determined that the chlorine used in bleaching was a factor in high AOX values, while values could be reduced by lowering the quantity of chlorine used. Chlorine dioxide was substituted for chlorine and reduced AOX values was the result. A typical bleaching sequence became C/D.Eo.D.E.D. with at least 50% of the chlorine being replaced by chlorine dioxide on an equivalence basis. Some paper mills have eliminated chlorine entirely by using D.Eo.D.E.D. Or O.D.Eo.D.E.D. sequences.




Ozone is a powerful bleaching agent used in many bleach plants throughout the world to bleach Kraft Pulp and recycled fibers. It has recently been discovered that ozone can replace chlorine dioxide and achieve the same brightness and pulp quality. It has been found that 1 kg of ozone can essentially replace 2


-4 kgClO2


. This results in lower cost bleaching sequences such as O.Z/D.Eop.D.E.D, O.D/Z.Eop.D.X.D, D/Z.Eop.D.E.D. and others. The use of ozone (O


3


) can become more attractive, however, if a more efficient and cost effective method can be found to better disperse and dissolve O


3


into an existing bleaching sequence. The usual method of bleaching with ozone comprises dispersing ozone into a medium consistency pulp using a pump, mixer and retention tube. This is carried out at a pressure of 150 psig and requires a compressor to add the ozone.




Medium consistency pulp generally contains a cellulose fiber suspension of from 8-15%, that when exposed to high shear forces acquires fluid properties that permits it to be pumped. High shear mixers enable gases to be dispersed and dissolved in medium consistency pulps.




A typical medium consistency ozone bleaching process generally consists of pumping pulp to a mixer where ozone is added. The gas dispersion in the pulp is then sent to a vertical retention tube where at least 90% of the ozone dissolves and reacts during a hydraulic residence time of 3060 secs. If the ozone utilization is low, then a second mixer may be added. On discharge from the retention tube, gas is separated from the pulp and the excess ozone in the gas is sent to an ozone destruct unit.




To achieve high utilization of ozone in medium consistency bleaching, a pump and mixer(s) are used that are driven by high HP motors and the power requirement can reach 0.5-1.0 HP/ton pulp/day. Typically pulp is bleached with an ozone charge of about 5 kg ozone/ton pulp, and this is added in a single stage. If higher charges of ozone are required then more than a single stage is necessary, e.g. 10 kg/ton requires two stages. The limiting factor in ozone addition is the volume of gas that can be dispersed and dissolved in the pulp with high ozone utilization. For medium consistency processes it has been found that a high utilization of ozone can be achieved if the volume ratio of gas in the total fluid mixture does not exceed 30%. For ozone generated at a concentration of 10% w/w and operating at a pressure of 150 psig, the maximum charge added is 5 kg of ozone/ton of pulp. If the ozone concentration is raised to 12% this charge can be raised to 6 kg/ton with the same ozone utilization.




An alternative to medium consistency pulp technology is that of using high consistency pulp. In this process fibers are dewatered to a consistency of 25-40% by passing medium consistency pulp through a press. As well as dewatering the fibers, the pulp is compressed and then fluffed in order to have good contact between gas and fibers. The pulp is then introduced into a reactor where it is contacted with ozone for a period of 1-3 minutes at a pressure of 5 psig. After ozonation, the pulp is degassed and diluted with wash water before passing on to a washing stage.




When this process was first started there were reports of uneven bleaching, but with improved reactor design this was overcome. An advantage of this process is that it does not require high concentrations of ozone, as using 6.0% w/w works very well. However the high consistency process is not widely accepted because of the mechanical complexity of the equipment and the high power requirement for dewatering the pulp.




Another possible technique for bleaching pulp involves low consistency pulp. Low consistency pulp employs a cellulose fiber suspension of 1-5% that has a viscosity greater than water, but can be pumped using conventional pumps without the need of a high shearing effect. Chlorination is generally carried out in a low consistency process and in many processes chlorine dioxide is also added to low consistency pulp slurries. However there has been little discussion of ozonation at low consistency.




Laboratory studies have been carried out on ozonating pulp in bubble columns using pulp slurries around 0.5% concentration. This method worked well, but with columns of a height of 25 m, the gas residence time was very short and ozone utilization low. Furthermore, ozone concentrations in the gas applied were low, 2-3% w/w.




This low concentration required large volumes of gas to obtain the desired ozone charge. The low concentration also led to low mass transfer rates. The net effect of this was poor ozone utilization, and this together with the dilute pulp slurry has made the consideration of using ozone with low consistency pulp commercially unattractive.




Up to this point, therefore, there has been no commercial process devoted to ozone bleaching of low consistency pulp. While some laboratory studies have been carried out at consistencies of about 0.5% using unpacked columns and adding the ozone by a diffuser at the bottom, such a process is not considered to be practical for commercial use. Furthermore, there are reports that O


3


consumption increases due to decomposition in water. Also the favored technology for bleaching uses medium consistency pulps and there have been no reported attempts to carry out low consistency ozone bleaching on an industrial scale.




Low consistency pulp, however, is easier to pump. Dispersing ozone onto it, because of its low viscosity, would therefore require less power. This can be done before or after a low consistency D stage or a medium consistency D stage. In the latter case this is carried preferably out in a downflow tower and at the bottom of the tower the pulp is diluted to low consistency in order to pump it to the next process step.




Hence if ozone can be effectively and efficiently dispersed and dissolved in low consistency pulp, the use of low consistency technology with ozonation offers a low cost method which can be used to retrofit an existing bleaching process.




Therefore, it is an object of the present invention to provide a novel process and apparatus for bleaching pulp using ozone.




Another object of the present invention is to provide a method for more effectively and efficiently dispersing and dissolving ozone into low consistency pulp so as to make low consistency pulp bleaching technology with ozone viable.




Still another object of the present invention is to provide an efficient process and apparatus for bleaching employing low consistency technology, whereby ozone is used as the bleaching agent.




These and other objects of the present invention will become apparent to the skilled artisan upon a review of the following disclosure, the Figures of the Drawing, and the claims appended hereto.




SUMMARY OF THE INVENTION




In accordance with the foregoing objectives, there is provided a novel process and apparatus for bleaching pulp with gaseous mixtures comprising ozone. The process of the present invention comprises first preparing a slurry of cellulosic pulp of a low consistency, i.e., a consistency of fibers of from about 1-5 weight %. Ozone is then mixed with the pulp slurry using high shear mixing. This high shear is preferably created using a mixer designed for medium consistency pulp bleaching, i.e., a mixer generally used for medium consistency pulps. Such high shear (high-intensity) mixers are well known in the art. Using the high shear mixing has been found to allow the ozone to be effectively and efficiently dispersed and dissolved into the low consistency pulp, even while the pulp mixture remains at low pressure. The ozone is then maintained in contact with the cellulosic fibers for a time sufficient to bleach the fibers, before separation occurs.




The process of the present invention offers one the energy benefits of using low consistency technology, in combination with the benefits of using ozone to bleach the cellulosic pulp. The ozone bleaching step of the present invention can be combined in an overall bleaching process with other bleaching steps. For example, the ozone bleaching step can be used either before or after a chlorine dioxide bleaching step. The ozone bleaching step can also be followed by a different bleaching step, e.g., with hydrogen peroxide.




Another advantage of the present invention is that when ozone is compressed at higher pressures, it breaks down to oxygen (O


2


). Thus, if a lower pressure can be used, more ozone should be available. Ozone also has a short half-life before converting to oxygen, therefore, the present invention with its short mixing time helps ensure more ozone is available for bleaching purposes.




In another embodiment, there is provided a system for a reactor for bleaching pulp at low consistency with ozone. The reactor comprises a high shear mixer wherein ozone is dispersed into a pulp slurry having a consistency in the range of from 1 to 5 wt %, and a retention tube connected to the mixer which operates at a pressure of from 20 to 60 psig, and wherein the ozone bleaches the pulp in the pulp slurry.











BRIEF DESCRIPTION OF THE DRAWING





FIG. 1

of the Drawing depicts a reactor for bleaching pulp at low consistency with ozone, which uses a pressurized ozone generator.





FIG. 2

of the Drawing depicts a reactor for bleaching pulp at low consistency with ozone employing an ozone compressor.





FIG. 3

of the Drawing depicts a low consistency ozone bleaching process carried out before a chlorine dioxide bleaching step.





FIG. 4

of the Drawing depicts an alternative low consistency ozone bleaching process carried out before a chlorine dioxide bleaching step.





FIG. 5

of the Drawing depicts a low consistency ozone bleaching process wherein the ozone bleaching step is carried out after a chlorine dioxide bleaching step.





FIG. 6

of the Drawing depicts an alternative low consistency ozone bleaching process using an ozone bleaching step that is carried out after a chlorine dioxide bleaching step.





FIG. 7

of the Drawing graphically depicts the D/Z delignification efficiency for various reactor/mixers at low consistency (2.5-3.5 wt %).











DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS




The ozone employed in the process of the present invention can be of any source. Preferably, the ozone is generated on-site using an ozone generator, to thereby produce ozone from oxygen at a concentration in the range of from about 5 to 20 wt %, more preferably in the range of from about 10 to 20 wt %, and most preferably in the range of from about 10 to 15 wt %. Ozone generators are well known, and are generally operated at a pressure in the range of from about 20-60 psig, and more preferably in the range of from 30-40 psig.




The ozone/oxygen mixture is preferably introduced into the high shear mixer through a valve, which can be used to control the flow of the gas mixture into the high shear mixer. The ozone/oxygen gas mixture can be compressed, if so desired, prior to introduction into the high shear mixer. The ozone compressor generally operates at a pressure ranging from 20-150 psig, and more preferably in the range of from 30-40 psig.




The high shear mixer can be any high shear mixer well known to the art of pulp bleaching. Such mixers are described, for example, in Pulp Bleaching—Principals and Practice by Carlton W. Dence and Douglas W. Reeve, TAPPI Press, 1996, pages 549-554. In high shear (high intensity) mixers, the pulp and ozone gas mixture are mixed by passage through zones of intense shear. They induce microscale mixing in the entire volume and not only in specific locations as in a continuous stirred reactor. The high shear is created by imposing high rotational speeds across narrow gap, generally between the rotor blades and reactor casing, through which the pulp suspension flows. Although there are design differences among the high shear mixers conventionally known, they all attempt to fluidize the suspension in the mixture working zone. The high shear rate insures flock disruption and good fiber scale mixing.




The present invention employs a high shear mixer, and many different high shear mixers used for pulp bleaching are known. Some of those known include the Ahlstrom Ahlmix, the Ahlstrom MC pump, the Beloit-Rauma R series, the Ingersoll-Rand Hi-Shear and the Impco Hi-Shear mixer from Beloit Corporation. Others include the Kamry MC, the Kamry MC Pump (Pilot) the Sunds SM and Sunds T mixers. The Quantum mixer is also an acceptable high shear mixer. All such mixers are known in the art and are generally used to mix medium consistency pulp suspensions.




Mixers can be compared based on energy applied (MJ/ton of pulp) and power dissipation (W/m


3


). J. R. Bourne in


Chem. Eng. Sci.,


38(1);5 (1983) states that all devices operated at the same power unit volume will generate the same rate of micromixing. This assumes energy applied equals energy dissipated, which is not true for all mixers. The distribution of power throughout the suspension is as important as its total. Examples of different mixers and the energy and power values for a given pulp consistency are as follows:























Power








Mixer




Consistency




Dissipation




Energy







Type




(wt %)




(W/m


3


)




(MJ/ton)





























Hand Mixing




3




  2 × 10


4






120







CSTR




2-3




600




5-9







Quantum (high)




5




4.5 × 10


5






 63







shear) Mixer







High Shear




10 




1.8 × 10


6






180















Using the measured energy dissipation rate and a correlation for the apparent viscosity of a pulp suspension given by Bennington in “Mixing Pulp Suspensions”, PhD. thesis, The University of British Columbia, Vancouver, B.C., 1988, τ is 0.02 sec. for a 10% consistency in a typical high shear mixer. In a CSTR operating at 3% consistency, τ=0.4 sec., but varies locally with the mixer. τ represents the mean lifetime of turbulent eddies.




The pulp suspension of the present invention that is provided to the high shear mixer is of low consistency. This means that the amount of pulp contained in the suspension ranges from about 1 to 5 wt %. More preferably, the amount of pulp in the suspension ranges from 2 to 4 wt %. Preferably, the temperature of the pulp slurry entering the mixer is in the range of from about 20-80° C., more preferably from about 40-60° C. The ozone charge added to the pulp is in the range of from about 2-10 kg/ton, more preferable from about 5-6 kg/ton.




Once in the high shear mixer, the ozone and pulp suspension are mixed in the high shear mixer in the range of from about 0.01 seconds to 10 seconds, and more preferably in the range of from about 0.1 seconds to 4 seconds. Once the mixing has taken place, the pulp suspension is then passed to a bleaching or reactor station, which is preferably a retention tube, wherein the residence time ranges from about 1 to 10 minutes, more preferably from about 2-5 minutes. It is in the retention tube that the bleaching of the pulp actually t place by the ozone. Because of the use of the high shear mixer, and the short time in which it takes to dissolve the ozone, as well as the low pressures under which the mixing and retention tube can operate, more ozone is available to do the bleaching of the low consistency pulp. Accordingly, the present invention provides surprising results with regard to excellent bleaching.




Referring to

FIG. 1

, there is illustrated a reactor for bleaching pulp at low consistency with ozone by using a pressurized ozone generator. It consists of a medium consistency mixer where ozone is dispersed in the low consistency pulp followed by a retention tube operating at a pressure between 20-60 psig where ozone gradually dissolves and bleaches the pulp.




Air is introduced by line


1


into an air separation unit


2


where oxygen is separated from air. Oxygen passes by line


3


into an ozone generator


4


and is converted to ozone, and this passes through line


5


into a control valve


6


that automatically regulates the gas flow by gas flowmeter


7


. Ozone gas is introduced to the mixer


9


by an inlet line


8


and is dispersed into the low consistency pulp. Pulp slurry passes through line


20


into pump


21


where it is pumped into the mixer


9


and mixed with the ozone-oxygen mixture.




The pulp slurry-gas mixer passes into the column


23


that is held under pressure by a back pressure valve


24


. The ozone-oxygen mixture dissolves and reacts with the pulp slurry before exiting through valve


24


into line


25


.




The pulp slurry-gas mixture flows into a separator vessel


26


where gases are separated from the pulp and flow through line


27


into an ozone destruct unit


28


, where the ozone is destroyed and the remaining gases leave through line


29


. The pulp slurry leaves the separator through line


30


and flows into pump


31


where it is pumped to the next stage through line


32


.





FIG. 2

illustrates a reactor for bleaching pulp at low consistency with ozone by using an ozone compressor. It comprises generally of a medium consistency mixer where ozone is dispersed in the low consistency pulp, followed by a retention tube operating at a pressure between 20-60 psig where ozone gradually dissolves and bleaches the pulp.




Air is introduced by line


100


into an air separation unit


102


where an oxygen rich stream is separated from air. Oxygen passes by line


103


into an ozone generator


104


and is converted to ozone and this passes through line


105


into an ozone compressor


110


where the gas mixture is compressed. From here it flows to a control valve


106


that automatically regulates the gas flow by gas flowmeter


107


. Ozone gas is introduced to the mixer


109


by an inlet line


108


and is dispersed into the low consistency pulp. Pulp slurry passes through line


120


into pump


121


where it is pumped into the mixer


109


via line


122


and mixed with the ozone-oxygen mixture.




The pulp slurry-gas mixture passes into the column


123


that is held under pressure by a back pressure valve


124


. The ozone-oxygen mixture dissolves and reacts with the pulp slurry before exiting through valve


124


into line


125


. The pulp slurry-gas mixture flows into a separator vessel


126


where gases are separated from the pulp and flow through line


127


into an ozone destruct unit


128


, where the ozone is destroyed and the gases leave through line


129


. The pulp slurry leaves the separator through line


130


and flows into pump


131


where it is pumped to the next stage through line


132


.





FIG. 3

illustrates a low consistency ozone bleaching process in accordance with the present invention that includes an ozone bleaching stage before a chlorine dioxide bleaching stages. This uses a pressurized ozone generator to compress ozone before adding it to a mixer. This method avoids the use of a compressor to add compressed ozone to the mixer.




In the process, pulp of medium consistency is pumped through line


252


into a storage tank


251


. The pulp flows down the tank into a dilution zone


250


where it is diluted to a low consistency with dilution water added through nozzles


246


and


247


. Agitators


248


and


249


ensure that mixing is complete. The pulp slurry of consistency about 3% passes through line


220


into pump


221


where it is pumped into the mixer


209


and mixed with the ozone-oxygen mixture. Air is introduced by line


201


into an air separation unit


202


where oxygen is separated from air. Oxygen passes by line


203


into a pressurized ozone generator


204


and is converted to ozone and this oxygen-ozone mixture passes through line


205


into a control valve


206


that automatically regulates the gas flow by gas flowmeter


207


. The ozone-oxygen gas mixture is introduced to the mixer


209


by an inlet line


208


and is dispersed into the low consistency pulp.




The pulp slurry-gas mixture passes into the column


223


, that is held under pressure by a back pressure valve


224


. The ozone-oxygen mixture dissolves and reacts with the pulp slurry before exiting through valve


224


into line


225


. The pulp slurry-gas mixture flows into a separator vessel


226


, where gases are separated from the pulp and flow through line


227


into an ozone destruct unit


228


, where the ozone is destroyed and the resulting gases leave through line


229


. The pulp slurry leaves the separator


226


through line


230


and flows into pump


231


, where it is pumped through line


232


into a mixer


234


where chlorine dioxide is added through line


233


before flowing by line


235


into the bottom of the bleaching tower


236


. The pulp rises to the top of the tower and overflows through line


237


into line


238


to a washer


239


. The pulp is washed with wash water added through line


240


and the washed pulp leaves the washer through line


241


. The dilution water separated from the pulp is collected in storage tank


242


, where it is removed through line


243


by pump


244


and is pumped through line


245


to the nozzles


246


and


247


, where it is added to the dilution zone


250


of the storage tank


251


.





FIG. 4

illustrates a low consistency ozone bleaching process involving an ozone bleaching stage in accordance with the present invention that is carried out before a chlorine dioxide bleaching stage. The process uses a compressor to compress ozone before adding it to the mixer.




In the figure, pulp of medium consistency is pumped through line


352


into a storage tank


351


. The pulp flows down the tank into a dilution zone


350


where it is diluted to a low consistency with dilution water added through nozzles


346


and


347


. Agitators


348


and


349


ensure that mixing is complete. The pulp slurry of consistency about 3% passes through line


320


into pump


321


where it is pumped through line


322


into the mixer


309


and mixed with the ozone-oxygen mixture. Air is introduced by line


301


into an air separation unit


302


where oxygen is separated from air. Oxygen passes by line


303


into an ozone generator


304


and is converted to ozone, and this oxygen-ozone mixture passes through line


305


into an ozone compressor


310


where it is compressed. From here it flows to a control valve


306


that automatically regulates the gas flow by gas flowmeter


307


. The ozone gas mixture is introduced to the mixer


309


by an inlet line


308


and is dispersed into the low consistency pulp.




The pulp slurry-gas mixture passes into the column


323


, which is held under pressure by a back pressure valve


324


. The ozone-oxygen mixture dissolves and reacts with the pulp slurry before exiting through valve


324


into line


325


. The pulp slurry-gas mixture flows into a separator vessel


326


where gases are separated from the pulp and flow through line


327


into an ozone destruct unit


328


, where the ozone is destroyed and the gases leave through line


329


. The pulp slurry leaves the separator through line


330


and flows into pump


331


where it is pumped through line


332


into a mixer


334


where chlorine dioxide is added through line


333


before flowing by line


335


into the bottom of the bleaching tower


336


. The pulp rises to the top of the tower and overflows through line


337


into line


338


to a washer


339


. The pulp is washed with wash water added through line


340


and the washed pulp leaves the washer through line


341


. The dilution water separated from the pulp is collected in storage tank


342


. It is removed through line


343


entering pump


344


and is pumped through line


345


to the nozzles


346


and


347


, where it is added to the dilution zone


350


of the storage tank


351


.





FIG. 5

depicts a low consistency ozone bleaching process stage in accordance with the present invention that is carried out after a chlorine dioxide bleaching stage. The process uses a pressurized ozone generator to produce compressed ozone before adding it to a mixer. This method avoids the use of a compressor to add compressed ozone to the mixer.




Pulp of medium consistency is pumped through line


452


into a storage tank


451


. The pulp flows down the tank into a dilution zone


450


where it is diluted to a low consistency with dilution water added through nozzles


446


and


447


. Agitators


448


and


449


ensure that mixing is complete. The pulp slurry, now of low consistency about 3%, passes through line


420


into pump


421


that discharges through line


422


into a mixer


424


where chlorine dioxide is added through line


423


. The pulp slurry-chlorine dioxide mixture passes through fine


425


into the bottom of tower


426


, where it flows upwards consuming chlorine dioxide and bleaching the pulp. It overflows from the tower


426


in line


427


flowing into pumps


428


, which discharges into mixer


409


where the oxygen-ozone mixture is added.




Air is introduced by line


401


into an air separation unit


402


where oxygen is separated from air. Oxygen passes by line


403


into an ozone generator


404


and is converted to ozone and this passes through line


405


into a control valve


406


that automatically regulates the gas flow by gas flowmeter


407


. Ozone gas is introduced to the mixer


409


by an inlet fine


408


and is dispersed into the low consistency pulp. The pulp slurry-gas mixture passes into the column


429


, which is held under pressure by a back pressure valve


430


. The ozone-oxygen mixture dissolves and reacts with the pulp slurry before exiting through valve


430


into line


431


. The pulp slurry-gas mixture flows into a separator vessel


432


, where gases are separated from the pulp and passed through line


433


into an ozone destruct unit


434


, in which the ozone is destroyed and the resultant gases leave through line


438


. The pulp slurry leaves the separator through line


436


and flows into pump


437


, where it is pumped to the washer


439


through line


460


. The pulp is washed with wash water added through line


440


and leaves through line


441


. The washings are collected in tank


442


and leave through line


443


entering pump


444


and discharges via line


445


through nozzles


446


and


447


into the dilution zone


450


of the medium consistency storage tank


451


.





FIG. 6

illustrates a low consistency ozone bleaching process in accordance with the present invention that is carried out after a chlorine dioxide bleaching step. The process uses a compressor after the ozone generator to compress ozone before adding it to a mixer.




Pulp of medium consistency is pumped through line


552


into a storage tank


551


. The pulp flows down the tank into a dilution zone


550


where it is diluted to a low consistency with dilution water added through nozzles


546


and


547


. Agitators


548


and


549


ensure that mixing is complete. The pulp slurry, now of consistency about 3%, passes through line


520


into pump


521


and discharges through line


522


into a mixer


524


where chlorine dioxide is added through line


523


. The pulp slurry-chlorine dioxide mixture passes through line


525


into the bottom of tower


526


, where it flows upwards consuming chlorine dioxide and bleaching the pulp. It overflows from the tower in line


527


flowing into pump


528


and discharges into mixer


509


where the oxygen-ozone mixture is added. Air is introduced by line


501


into an air separation unit


502


where oxygen is separated from air. Oxygen passes by line


503


into an ozone generator


504


and is converted to ozone, and this passes through line


505


into a compressor


510


where the gas is compressed. The oxygen-ozone mixture passes through control valve


506


, which automatically regulates the gas flow by gas flowmeter


507


. The ozone gas mixture is introduced to the mixer


509


by an inlet line


508


, and is dispersed into the low consistency pulp.




The pulp slurry-gas mixture passes into the column


529


, which is held under pressure by a back pressure valve


530


. The ozone-oxygen mixture dissolves and reacts with the pulp slurry before exiting through valve


530


into line


531


. The pulp slurry-gas mixture flows into a separator vessel


532


, where gases are separated from the pulp and flow through line


533


into an ozone destruct unit


534


, wherein the ozone is destroyed and the resultant gases leave through line


535


. The pulp slurry leaves the separator through line


536


and flows into pump


537


where it is pumped to the washer


539


through line


538


. The pulp is washed with wash water added through line


540


and leaves through line


541


. The washings are collected in tank


542


and leave through line


543


entering pump


544


and discharges via line


545


through nozzles


546


and


547


into the dilution zone


550


of the medium consistency storage tank


551


.




The invention will be illustrated in greater detail by the following specific example. It is understood that the example is given by way of illustration and is not meant to limit the disclosure or the claims to follow. All percentages in the examples, and elsewhere in the specification, are by weight unless otherwise specified.




EXAMPLE 1




It has been found that most pulps bleach well giving increased brightness with little strength loss for an ozone charge of 5 kg of ozone/ton pulp. Taking this is as the basis of a design for a reactor, and assuming ozone is generated at a concentration of 12% w/w, the oxygen requirement is estimated as follows:




O


2


required=100*5/12=41.7 kg/ton of pulp.




This produces a mixture of O


2


+O


3


=5 kg O


3


+36.7 kg O


2


.




The volume of the gases at a pressure of 760 mms Hg, and temperature of 0° C. is 2.76 m


3


O


3


+30.40 m


3


O


2


.




Total gas volume=33.16 m


3


/ton of pulp.




If this is to be dispersed and dissolved in a pulp slurry having a consistency of 3%, volume of pulp slurry=100/3 m


3


/ton of pulp=33.3 m


3


/ton of pulp.




This consists of 1.0 m


3


pulp+32.3 m


3


of dilution water.




Hence it is required to dissolve and disperse 33.16 m


3


of gas in 33.3 m


3


of pulp slurry.




The ratio of gas to pulp slurry=33.16:33.3=about 1:1.




If all the O


3


dissolved in the dilution water, the solubility of the O


3


would have to be 5 kg/32.3 m


3


, or 155 g/m


3


.




If this reaction takes place at 50° C., the solubility of 12% w/w O


3


in water is as follows:

















Total Pressure




Partial Pressure O


3






Solubility O


3








(psia)




(psia)




(g/m


3


)

























14.7




1.22




13.2






24.7




2.05




22.2






164.7




13.67




147.9














If this is compared to dispersing ozone in medium consistency pulp having a consistency of 10%:




Volume=1.0 m


3


pulp+9.0 m


3


dilution water=10.0 m


3


pulp slurry.




If 5 kg O


3


ton of pulp is dispersed and dissolved in the dilution water, O


3


applied=5 kg/9 m


3


=555 g/m


3


.




The gas to liquid ratio at a pressure of 760 mms Hg and 0° C. is 33.16:9, which is 3.7:1.




At a pressure of 150 psig, this ratio becomes 0.33:1




If this medium consistency equipment disperses ozone satisfactorily at a ratio of 0.33:1 for medium consistency pulp, it will be able to do the same for low consistency. Hence to reduce the gas:slurry ratio from 1:1 to 0.33, the gas volume must be reduced by a ratio of 1/0.33 m


3


. This corresponds to a pressure of 30 psig.




Based on the above calculations, it was decided that medium consistency equipment can be used for dispersing ozone into low consistency pulp at a pressure of 30 psig. This was confirmed by testing carried out in the Laboratory as follows:




Laboratory Studies




Trials were carried out in a Quantum Mark-5 Laboratory Mixer/Reactor. This was originally designed and operated with medium consistency pulp. For each run 90 grams of pulp having Kappa No=25.5 was used and a first bleaching stage at a temperature of 40° C. with a constant chlorine dioxide dosage of 14.5 kg/ton was carried out. Following this, 4.0-5.5% w/w ozone-oxygen mixture was then introduced at a pressure of 50-70 psig at a temperature of 40° C. During the ozone addition, the pulp was mixed for 5 seconds at high intensity using a Quantum mixer followed by subsequent intermittent mixing at a lower intensity (using a CSTR) for 5 minutes. The results are shown in Table 1 below:
















TABLE 1












Retention







O


3


Charge




O


3


Consumed




O


3


Reacted




Time




Pressure






(kg/t)




(kg/t)




(%)




(mins)




(psig)











2.4




2.2




93.0




5




46






4.0




3.9




95.0




5




55






6.1




5.8




95.1




5




52






7.3




7.0




95.9




5




65














This illustrates that equipment designed for dispersing gases in medium consistency pulp can also be used successfully for O


3


bleaching of low consistency pulp with high ozone utilization.




EXAMPLE 2




Tests were carried out on a Pilot Plant that was originally designed to use ozone to bleach a medium consistency pulp slurry. It consists of a pump that pumps the pulp into a pressurized high shear mixer. Ozone of concentration 12% w/w is compressed and added to the pulp slurry at the inlet of the mixer. The ozone gas mixture is dispersed in the pulp slurry where it reacts with the lignin. The slurry-gas mixture discharges into a column where the remaining ozone is consumed.




Results for a Softwood Pulp having Kappa No 31, carried out at temperature 40° C. and a pulp consistency of 3.5%, are shown in Table 2 below:
















TABLE 2










Ozone






Ozone






Ozone




Pressure




Pressure




Ozone




Consumed






Charge




inlet




Bottom




Consumed




top






to pulp




Mixer




Tower




in Mixer




Tower






(kg/t)




(psig)




(psig)




(%)




(%)



























6.3




30




20




87




99






6-3




90




80




94




99






6-3




110




100




99




99














These results demonstrate that a Mixer designed for dispersing ozone into a medium consistency pulp slurry can be used successfully for a low consistency pulp slurry and that it is possible to operate at lower pressures with good results.




EXAMPLE 3




Two runs of an ozone stage were performed on a brown stock kraft pulp at low consistency in a Pilot plant using a high intensity mixer. The runs were made to verify if the ozone stage efficiency (degree of delignification) and the consumption were equivalent for low and medium consistency pulp. The pulp used was a softwood kraft with an initial kappa number of 30.8 and ISO brightness of 27.9%.




In each run, the washed pulp was received at 33% consistency and diluted to 3.8% consistency in an agitated feed tank. Pulp slurry was then preheated to 40° C. with the injection of steam in the feed tank. At that temperature, concentrated (98%) sulphuric acid was added to the tank to adjust the pH of the pulp suspension to 2.5 before the ozone stage. Pulp slurry was pumped directly to the hopper of the positive displacement pump. This pump introduced pulp in the high pressure section of the pilot plant, where ozone gas was mixed with the pulp in a Impco high intensity mixer. The flow of the pulp into the high pressure section and the ozone charge and concentration were kept constants.




After compression, the ozone gas stream was introduced into the pulp suspension trough a sintered metal sparger (20 micron porosity) located between the feed pump discharge and the Impco high intensity mixer inlet. The residence time in that mixer was approximately 0.05 second. The conditions for each run are described in Table 3.




The pulp was sampled approximately 1 meter from the ozone injector point after passing through the high intensity mixer. Gas samples were removed at the exit of the high intensity mixer, at the medium consistency pulp sampling point and at the top of the tower. Each gas sample was analyzed for residual concentration by gas chromatography. The ozonated pulp for the second run was analyzed for kappa number (CPPA standard, G.18) and ISO brightness (CPPA standard, E.1). The results are shown in Table 4 below.




The efficiency of delignification was approximately 1 kappa number drop per kg ozone. This observation is comparable to the efficiency observed at medium consistency and demonstrates the successful and efficient use of a high shear mixer with ozone and low consistency pulp.












TABLE 3











Z-stage conditions















Conditions




First Run




Second Run



















Consistency, %




3.8




3.8







Temperature, ° C.




40




40







pH




2.4




2.4







Ozone charge, % o.d. pulp




0.551




0.566







Ozone concentration, %




12.85




13.21







Pressure




30




90







Residence time,




6.4




6.4







min





























TABLE 4














First Run





Second Run


















Results




Bottom




Top




Bottom




Top





















Ozone residual, %




0.072




0.001




0.037




0.001







on o.d. pulp







Ozone consumed, %




0.479




0.550




0.530




0.565







on o.d. pulp







Kappa






27.0




24.1







Brightness ISO, %






31.4




32.2







Viscosity, CP






25.3




23.3













Initial kappa: 30.8 and brightness % ISO: 27.9, 39.5 CP













EXAMPLE 4




The performance of continuously stirred tank reactors (CSTR) of different types was compared to a high shear mixer for delignification efficiency in a D/Z process at low consistency. The performances were compared on the basis of OXE (oxidation equivalent, with 1 OXE=quantity of substance which receives 1 mole electrons when the substance is reduced. ClO


2


=74.12 OXE/Kg and O


3


=125.00 OXE/Kg). All of the CSTRs considered were similar in setup in terms of ozone pressure, concentration and duration.




The various reactors/mixers run, with the results are as follows.




CRL: (D/Z)Ep, SKP, initial kappa No. 23.3, final kappa No. 3.6, 14.0 kg ClO


2


ton for 6.3 kg O


3


/ton




AL: (D/Z)Eop, SKP, initial kappa No. 24.0, final kappa No. 7.9, 8.0 kg ClO


2


/ton, 6.33 kg/O


3


/ton




ECONOTECH: (D/Z)Ep, SKP, initial kappa No. 23.3, final kappa No. 3.6, 14.0 kg ClO


2


/ton, 6.0 kg O


3


/ton




CTP: (D/Z)Ep, SKP, initial kappa No. 25.4, final kappa No. 5.1, 15.0 kg ClO


2


/ton, 5.3 kg O


3


/ton




QUANTUM: (D/Z)Ep, SKP, initial kappa No. 25.5, final kappa No. 4.5, 10.0 kg ClO


2


/ton, 4.0 kg O


3


/ton




ROBIN: (D/Z)Ep, SKP, initial kappa No. 25.4, final kappa No. 9.0, 9.3 kg ClO


2


/ton, 8.1 kg O


3


/ton




The delignification efficiency for the various reactors is graphically depicted in FIG.


7


. The results clearly demonstrate the superiority of using a high shear mixer in connection with ozone at low consistency, as compared to other reactors which are conventionally used with low consistency pulp.




While the invention has been described with preferred embodiments, it is to be understood that variations and modifications may be resorted to as will be apparent to those skilled in the art. Such variations and modifications are to be considered within the purview and the scope of the claims appended hereto.



Claims
  • 1. A process for bleaching pulp with ozone, which comprises:preparing a slurry of cellulosic pulp having a consistency in fibers of from 1 to less than 5 weight %, wherein a temperature of the pulp slurry is in the range of from 20 to 80° C.; adding ozone to the cellulosic pulp under high shear mixing conditions, an amount of the ozone added to the pulp is in the range of from about 2-10 kg/ton of pulp; and maintaining the ozone in contact with the cellulosic fibers under the high shear mixing conditions for a period of time ranging from 0.01-4 seconds thereby consuming 87-99% of the ozone.
  • 2. The process for bleaching pulp of claim 1, wherein after expiration of the time period the cellulosic pulp and any non-consumed portion of the ozone are passed into a pressurized retention tube where the non-consumed portion of the ozone reacts with lignin in the cellulosic pulp.
  • 3. The process for bleaching pulp of claim 1, wherein the cellulosic pulp and any ozone in the retention tube not reacted with the lignin leaves the retention tube through a pressure control valve and is discharged into a separate vessel, where the any ozone not reacted with the lignin in the retention tube is passed into an ozone destruct unit and thereafter vented to the atmosphere, and the cellulosic pulp from the retention tube is passed to a subsequent bleaching stage.
  • 4. The process for bleaching pulp of claim 3, wherein the residence time within the retention tube ranges from 1-10 minutes.
  • 5. The process for bleaching pulp of claim 3, wherein the subsequent bleaching stage involves chlorine dioxide as the bleaching agent.
  • 6. The process for bleaching pulp of claim 1, wherein the ozone used in the process is generated onsite from oxygen in a pressurized ozone generator.
  • 7. The process for bleaching pulp of claim 6, wherein the ozone generator produces ozone from oxygen at a concentration in the range of 10-25%.
  • 8. The process for bleaching pulp of claim 6, wherein the ozone generator operates at a pressure in the range of from about 20-60 psig.
  • 9. The process for bleaching pulp of claim 6, wherein the pulp slurry consistency is in the range of from 3-4 weight %.
  • 10. The process for bleaching pulp of claim 6, wherein the ozone is maintained in contact with the cellulosic fibers under the high shear mixing conditions for a time period ranging from 0.1 to 4 seconds.
  • 11. The process for bleaching pulp of claim 6, wherein after expiration of the time period the cellulosic pulp and any non-consumed portion of the ozone are passed into a pressurized retention tube where the non-consumed portion of the ozone reacts with lignin in the cellulosic pulp, a residence time of the cellulosic pulp within the retention tube ranging from 1-10 minutes.
  • 12. The process of claim 6, in which the ozone generator produces ozone from oxygen at a concentration of from 10-20%.
  • 13. The process of claim 6, wherein the ozone generator is operated at a pressure of from about about 20-60 psig.
  • 14. The process of claim 6, wherein the ozone generator is operated at a pressure of from about about 30-40 psig.
  • 15. The process of claim 1, wherein temperature of the pulp slurry entering the mixing with ozone is in the range of from 40 to 60° C.
  • 16. The process for bleaching pulp of claim 1, wherein the ozone charge added to the pulp is in the range of from about 5-6 kg/ton of pulp.
  • 17. The process for bleaching pulp of claim 1, wherein the pulp slurry consistency is in the range of from 3-4 weight %.
  • 18. The process for bleaching pulp of claim 1, wherein the ozone is maintained in contact with the cellulosic fibers under the high shear mixing conditions for a time period ranging from 0.1 to 4 seconds.
  • 19. A process for bleaching pulp with ozone, which comprises:preparing a slurry of cellulosic pulp having a consistency in fibers of from 1 to less than 5 weight %; adding ozone to the cellulosic pulp under high shear mixing conditions; maintaining the ozone in contact with the cellulosic fibers under the high shear mixing conditions for a period of time ranging from 0.01-4 seconds thereby consuming 87-99% of the ozone; the cellulosic pulp and any non-consumed portion of the ozone are passed into a pressurized retention tube after expiration of the time period, wherein the non-consumed portion of the ozone reacts with lignin in the cellulosic pulp; cellulosic pulp and any ozone in the retention tube not reacted with the lignin is allowed to leave the retention tube through a pressure control valve and is discharged into a separate vessel; and any ozone not reacted with the lignin in the retention tube is passed into an ozone destruct unit and thereafter vented to the atmosphere.
  • 20. The process for bleaching pulp of claim 19, wherein the cellulosic pulp from the retention tube is passed to a subsequent bleaching stage.
  • 21. The process for bleaching pulp of claim 19, wherein the ozone used in the process is generated onsite from oxygen in a pressurized ozone generator.
  • 22. The process for bleaching pulp of claim 21, wherein the ozone generator produces ozone from oxygen at a concentration in the range of 10-25%.
  • 23. The process for bleaching pulp of claim 21, wherein the ozone generator operates at a pressure in the range of from about 20-60 psig.
  • 24. The process of claim 21, in which the ozone generator produces ozone from oxygen at a concentration of from 10-20%.
  • 25. The process of claim 21, wherein the ozone generator is operated at a pressure of from about about 20-60 psig.
  • 26. The process of claim 21, wherein the ozone generator is operated at a pressure of from about about 30-40 psig.
  • 27. The process for bleaching pulp of claim 19, wherein an amount of the ozone added to the pulp is in the range of from about 2-10 kg/ton of pulp.
  • 28. The process for bleaching pulp of claim 27, wherein the amount of the ozone charge added to the pulp is in the range of from about 5-6 kg/ton of pulp.
  • 29. The process for bleaching pulp of claim 19, wherein the pulp slurry consistency is in the range of from 3-4 weight %.
  • 30. The process for bleaching pulp of claim 19, wherein the ozone is maintained in contact with the cellulosic fibers under the high shear mixing conditions for a time period ranging from 0.1 to 4 seconds.
  • 31. The process for bleaching pulp of claim 19, wherein a residence time of the cellulosic fibers within the retention tube is in the range of from 1-10 minutes.
  • 32. The process for bleaching pulp of claim 19, wherein a temperature of the pulp slurry just before undergoing the high shear mixing conditions is in the range of from 20 to 80° C.
  • 33. The process for bleaching pulp of claim 19, wherein the subsequent bleaching stage involves chlorine dioxide as the bleaching agent.
  • 34. The process of claim 19, wherein temperature of the pulp slurry entering the mixing with ozone is in the range of from 40 to 60° C.
Parent Case Info

This application is a continuation of application Ser. No. 10/201,248, filed on Jul. 24, 2002, now U.S. Pat. No. 6,579,412 which is a continuation of Ser. No. 09/559,993, filed Apr. 27, 2000, now abandoned, which is a continuation of Ser. No. 09/074,517 filed May 8, 1998, now abandoned, which is incorporated by reference herein.

US Referenced Citations (4)
Number Name Date Kind
4842690 Gazdik et al. Jun 1989 A
5346588 Sixta et al. Sep 1994 A
5853536 Hornsey et al. Dec 1998 A
6579412 Sundaram et al. Jun 2003 B2
Foreign Referenced Citations (2)
Number Date Country
2078276 Mar 1994 CA
WO 9315264 Aug 1998 WO
Continuations (3)
Number Date Country
Parent 10/201248 Jul 2002 US
Child 10/463156 US
Parent 09/559993 Apr 2000 US
Child 10/201248 US
Parent 09/074517 May 1998 US
Child 09/559993 US