CA2484557A1 - Low consistency oxygen delignification process - Google Patents
Low consistency oxygen delignification process Download PDFInfo
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- CA2484557A1 CA2484557A1 CA002484557A CA2484557A CA2484557A1 CA 2484557 A1 CA2484557 A1 CA 2484557A1 CA 002484557 A CA002484557 A CA 002484557A CA 2484557 A CA2484557 A CA 2484557A CA 2484557 A1 CA2484557 A1 CA 2484557A1
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- Prior art keywords
- slurry
- pulp
- oxygen
- mixing
- pulp slurry
- Prior art date
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 title claims abstract description 47
- 239000001301 oxygen Substances 0.000 title claims abstract description 47
- 229910052760 oxygen Inorganic materials 0.000 title claims abstract description 47
- 238000000034 method Methods 0.000 title claims abstract description 37
- 239000002002 slurry Substances 0.000 claims abstract description 31
- 239000013055 pulp slurry Substances 0.000 claims abstract description 27
- 239000000835 fiber Substances 0.000 claims abstract description 10
- 239000011541 reaction mixture Substances 0.000 claims abstract description 9
- 239000007789 gas Substances 0.000 claims description 12
- 239000003518 caustics Substances 0.000 claims description 11
- 229920005610 lignin Polymers 0.000 claims description 7
- 239000007844 bleaching agent Substances 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 238000005406 washing Methods 0.000 claims description 5
- 229910052979 sodium sulfide Inorganic materials 0.000 claims description 3
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 21
- 239000003513 alkali Substances 0.000 abstract description 6
- 239000011122 softwood Substances 0.000 abstract description 4
- 239000011121 hardwood Substances 0.000 abstract description 3
- 230000014759 maintenance of location Effects 0.000 description 6
- 239000007787 solid Substances 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 150000003464 sulfur compounds Chemical class 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 229910001882 dioxygen Inorganic materials 0.000 description 2
- VDQVEACBQKUUSU-UHFFFAOYSA-M disodium;sulfanide Chemical compound [Na+].[Na+].[SH-] VDQVEACBQKUUSU-UHFFFAOYSA-M 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012263 liquid product Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-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
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/147—Bleaching ; Apparatus therefor with oxygen or its allotropic modifications
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Paper (AREA)
Abstract
The present invention provides for a method for delignifying softwood or hardwood pulp in a fiber line of a pulp and papermaking system having a slurry at low consistency by adding to the pulp slurry oxygen and adding this pulp slurry reaction mixture to a reaction system comprising an efficient mixer and contact tank. The reaction system is preferably physically located after the knotters and before the brown stock washers to make more effective use the residual alkali and heat content in the incoming black liquor.
Description
LOW CONSISTENCY OXYGEN DELIGNIF'ICATION PROCESS
This application claims priority from US Provisional Patent Application Serial No. 60/ 514,946 filed October 28, 2003.
BACKGROUND OF THE INVENTION
The present invention relates to a method for delignifying softwood or hardwood pulp in a slurry at low consistency using a reaction device and oxygen.
Oxygen delignification of cellulosic material is generally practiced at medium consistency (8 to 16%) a region where it has been determined makes it both relatively easy to operate and economical. In such operations partially delignified pulp is reacted with oxygen in the presence of alkali ( pH >
11 ) using high shear mixers and pressurized upflow reactors with retention times of 20 to 60 minutes at pressure in excess of 90 psi and temperatures as high as 110° C. The high shear mixers facilitate the contacting of the pulp slurry with the oxygen containing gas in a very turbulent state lasting a few seconds prior to entering the pressurized vessels.
Using such equipment in single and two-stage configurations have resulted in reported delignification of up to 45%. However, many of such systems perform below 40% kappa reduction due to less than optimal contacting of oxygen with the pulp. In addition, implementation of medium consistency oxygen delignification require high capital expenditures for high shear mixers, medium consistency pumps and large contact towers and have thus far excluded many mills from economically modifying their processes and taking advantage of this technology. Low consistency oxygen delignification has not been practiced Commercially due to cost of chemicals and steam that would be required.
Oxygen delignification systems have traditionally been located after the brownstock washers on a fiber line where the slurry is relatively cold and have been stripped of all caustic thus requiring the addition of the full complement of steam and caustic. As a result of the high capital cost, energy costs and anticipated higher cost of chemicals, low consistency, or below 8% cellulosic material, oxygen delignification has not been practiced commercially.
SUMMARY OF THE INVENTION
The present invention provides a method for delignifying softwood or hard wood pulp in a slurry at low consistency by adding to the pulp slurry oxygen and adding this pulp slurry reaction mixture to a reaction system comprising an efficient mixer and contact tank. Preferably the pulp is removed from the brownstock processing section ( between the blow tank and the bleach section of the papermaking system. The reaction system is physically located after the knotters and before the brown stock washers to make more effective use of the residual alkali and heat content in the incoming black liquor. The physical location of the reaction system can be at a convenient position along the papermaking system; only the pulp slurry that is removed is "fixed" in that it is removed from the point between the knotters and the brown stock washers.
For purposes of the present invention, "low consistency" is defined as that pulp containing less than 8% by weight of cellulosic material.
In practicing the methods of the present invention, the reaction system may also be physically located and the pulp slurry drawn from the section of the fiber line after the digester and before the brown stack washers , or in between any two stages of a multi-stage brownstock washing step.
The hot pulp slurry is taken from the knotters with the black liquor still present. The black liquor results from cooking pulpwood in an aqueous solution in the sulfate or kraft papermaking process. Steam may be added to heat the slurry as well as caustic which can be used to adjust the pH. Oxygen is injected into the mixture which is then sent to the gas liquid mixer. The pulp slurry containing the oxygen is mixed at conditions of temperature and pressure whereby the oxygen begins to react with the lignin to effect delignification. This reaction mixture is then sent from the mixer to a retention tank which is also capable of being kept at pressure, where the delignification reaction will continue further. The reaction products are then sent into a blow tank or a gas-liquid separator where reaction gases and unused oxygen gas is disengaged or removed from the liquid product and scrubbed and either vented to the atmosphere or recycled.
The invention may be implemented as a retrofit in existing mills as well as new ones at relatively IoW capital cost. The placement of the system takes advantage of the residual caustic and heat that will be present in the slurry as it leaves the knotters. Furthermore a low consisfiency oxygen delignification reaction will be easier to control compared to operations at medium and high consistencies of pulp. Accordingly low consistency oxygen delignification before the brown stock washers of a fiber line is achieved.
The reactor assembly consists of a controlled cavitation device or other efficient mixing device, coupled with a residence tank.
The heat and alkali requirements for the delignification reaction will be obtained primarily from the residual alkali and heat content in the incoming black liquor and an oxygen containing gas.
This application claims priority from US Provisional Patent Application Serial No. 60/ 514,946 filed October 28, 2003.
BACKGROUND OF THE INVENTION
The present invention relates to a method for delignifying softwood or hardwood pulp in a slurry at low consistency using a reaction device and oxygen.
Oxygen delignification of cellulosic material is generally practiced at medium consistency (8 to 16%) a region where it has been determined makes it both relatively easy to operate and economical. In such operations partially delignified pulp is reacted with oxygen in the presence of alkali ( pH >
11 ) using high shear mixers and pressurized upflow reactors with retention times of 20 to 60 minutes at pressure in excess of 90 psi and temperatures as high as 110° C. The high shear mixers facilitate the contacting of the pulp slurry with the oxygen containing gas in a very turbulent state lasting a few seconds prior to entering the pressurized vessels.
Using such equipment in single and two-stage configurations have resulted in reported delignification of up to 45%. However, many of such systems perform below 40% kappa reduction due to less than optimal contacting of oxygen with the pulp. In addition, implementation of medium consistency oxygen delignification require high capital expenditures for high shear mixers, medium consistency pumps and large contact towers and have thus far excluded many mills from economically modifying their processes and taking advantage of this technology. Low consistency oxygen delignification has not been practiced Commercially due to cost of chemicals and steam that would be required.
Oxygen delignification systems have traditionally been located after the brownstock washers on a fiber line where the slurry is relatively cold and have been stripped of all caustic thus requiring the addition of the full complement of steam and caustic. As a result of the high capital cost, energy costs and anticipated higher cost of chemicals, low consistency, or below 8% cellulosic material, oxygen delignification has not been practiced commercially.
SUMMARY OF THE INVENTION
The present invention provides a method for delignifying softwood or hard wood pulp in a slurry at low consistency by adding to the pulp slurry oxygen and adding this pulp slurry reaction mixture to a reaction system comprising an efficient mixer and contact tank. Preferably the pulp is removed from the brownstock processing section ( between the blow tank and the bleach section of the papermaking system. The reaction system is physically located after the knotters and before the brown stock washers to make more effective use of the residual alkali and heat content in the incoming black liquor. The physical location of the reaction system can be at a convenient position along the papermaking system; only the pulp slurry that is removed is "fixed" in that it is removed from the point between the knotters and the brown stock washers.
For purposes of the present invention, "low consistency" is defined as that pulp containing less than 8% by weight of cellulosic material.
In practicing the methods of the present invention, the reaction system may also be physically located and the pulp slurry drawn from the section of the fiber line after the digester and before the brown stack washers , or in between any two stages of a multi-stage brownstock washing step.
The hot pulp slurry is taken from the knotters with the black liquor still present. The black liquor results from cooking pulpwood in an aqueous solution in the sulfate or kraft papermaking process. Steam may be added to heat the slurry as well as caustic which can be used to adjust the pH. Oxygen is injected into the mixture which is then sent to the gas liquid mixer. The pulp slurry containing the oxygen is mixed at conditions of temperature and pressure whereby the oxygen begins to react with the lignin to effect delignification. This reaction mixture is then sent from the mixer to a retention tank which is also capable of being kept at pressure, where the delignification reaction will continue further. The reaction products are then sent into a blow tank or a gas-liquid separator where reaction gases and unused oxygen gas is disengaged or removed from the liquid product and scrubbed and either vented to the atmosphere or recycled.
The invention may be implemented as a retrofit in existing mills as well as new ones at relatively IoW capital cost. The placement of the system takes advantage of the residual caustic and heat that will be present in the slurry as it leaves the knotters. Furthermore a low consisfiency oxygen delignification reaction will be easier to control compared to operations at medium and high consistencies of pulp. Accordingly low consistency oxygen delignification before the brown stock washers of a fiber line is achieved.
The reactor assembly consists of a controlled cavitation device or other efficient mixing device, coupled with a residence tank.
The heat and alkali requirements for the delignification reaction will be obtained primarily from the residual alkali and heat content in the incoming black liquor and an oxygen containing gas.
The amount of oxygen present can be an excess so as to react with some of the organic acids in the black liquor to reduce the heat value of the black liquor, and to react with sulfur compounds in the black liquor to reduce or eliminate the potential for total reduced sulfur (TRS) emissions.
A further advantage of the present invention is that un-oxidized white liquor is employed as the source of needed alkali. Additionally the excess oxygen is employed to oxidize some of the sulfur compounds in the white liquor.
BRIEF DESCRIPTION OF THE DRAWINGS
The figure is a schematic representation of an oxygen delignification process according to the practice of the present invention.
DETAILED DESCRIPTION OF THE INVENTION
The present invention provides for the low consistency oxygen delignification of pulp and comprises the following steps:
Taking pulp slurry at consistencies between 2 to 8% from the fiber line, at an appropriate location;
The pulp slurry drawn from the fiber line may be removed between the knotters and the brown stock washers, or before the brown stock washers and after the digester, or in between any two stages of a multi-stage brownstock washing step.
When necessary, adding a small amount of caustic to bring the slurry pH to at least 11 to 12;
Adding steam (when needed) to bring slurry temperature to between 5 85° C to 120° C;
Introducing the slurry and an oxygen containing gas into a high efficiency mixer for intense mixing under pressure of between 20 and 160 psig for up to 2 minutes;
Sending the slurry and oxygen mixture to a holding tank and maintaining it under pressure of 20 to 160 psig far 5 to 30 minutes;
Sending the reaction mixture to a disengagement tank where the reaction gases are separated from the slurry and sent for treatment and disposal; and Sending the slurry to the next stage in the bleach line of the papermaking process, which could be the screens or brown stock washers.
In the embodiment shown in Figure 1, pulp slurry from the knotters is contacted with oxygen in the presence of caustic, temperature and allowed a short residence time in a retention tank for the oxygen to react with and delignify the pulp. The oxygen also reacts with the organic solid in the black liquor resulting in a reduction of the heat value of the black liquor going to the recovery boiler. Additional reactions take place between the oxygen and sulfur compounds in the liquor, thus reducing or eliminating potential sources of total reduced sulfur (TRS) emissions by the pulp mill.
In the process, pulp slurry from the knotters with the black liquor still present and at a consistency of between 2 to 8% is transferred by a pump 30 through pipelines 10 and 40 to a steam mixer 50. Caustic, if needed may be added to the pulp slurry through side pipe 20 to maintain the pH of the pulp slurry between 11 and 12. At the steam mixer, steam is added to the pulp slurry through pipe line 130 to bring the temperature of the slurry to between 90 and 110° C before it flows into the efficient mixing device which could be a cavitation, type reactor 70 through line 60. Oxygen containing gas is introduced through a side inlet 140 and enters the efficient mixing device with the pulp slurry stream.
The pulp slurry and the oxygen containing gas are brought into intimate contact by the shearing and cavitation and mechanical forces generated as the rotor rotates at a high speed in the mixing device 70. The contacting is performed under suitable conditions of temperature and pressure whereby the oxygen begins to react with the lignin under caustic conditions to effect delignification. The reaction mixture proceeds through pipe line 80 into a retention tank 90 where under conditions of temperature, pressure and time the delignification reaction is continued further.
In order for the reaction to proceed as mentioned above, an oxygen containing gas must be used. Preferably oxygen with a minimum purity of 93% is employed. The preferred total reaction pressure should be not less than 80 psig and more preferably above 90 psig. The preferred minimum reaction temperature is 90° C but could be as high as 110° C.
The residence time of the reaction mixture in the retention tank is not less than 10 minutes but preferably up to 30 minutes. The reaction mixture is vVithdrawn through outlet 100 into a blow tank or gas-liquid separator 110 where reaction gases and unused oxygen gas disengages from the liquid product and is scrubbed and vented. The pulp sl~srry is withdrawn through line 120 and sent to the washing stage of the bleach line of the pulp and papermaking process.
A further advantage of the present invention is that un-oxidized white liquor is employed as the source of needed alkali. Additionally the excess oxygen is employed to oxidize some of the sulfur compounds in the white liquor.
BRIEF DESCRIPTION OF THE DRAWINGS
The figure is a schematic representation of an oxygen delignification process according to the practice of the present invention.
DETAILED DESCRIPTION OF THE INVENTION
The present invention provides for the low consistency oxygen delignification of pulp and comprises the following steps:
Taking pulp slurry at consistencies between 2 to 8% from the fiber line, at an appropriate location;
The pulp slurry drawn from the fiber line may be removed between the knotters and the brown stock washers, or before the brown stock washers and after the digester, or in between any two stages of a multi-stage brownstock washing step.
When necessary, adding a small amount of caustic to bring the slurry pH to at least 11 to 12;
Adding steam (when needed) to bring slurry temperature to between 5 85° C to 120° C;
Introducing the slurry and an oxygen containing gas into a high efficiency mixer for intense mixing under pressure of between 20 and 160 psig for up to 2 minutes;
Sending the slurry and oxygen mixture to a holding tank and maintaining it under pressure of 20 to 160 psig far 5 to 30 minutes;
Sending the reaction mixture to a disengagement tank where the reaction gases are separated from the slurry and sent for treatment and disposal; and Sending the slurry to the next stage in the bleach line of the papermaking process, which could be the screens or brown stock washers.
In the embodiment shown in Figure 1, pulp slurry from the knotters is contacted with oxygen in the presence of caustic, temperature and allowed a short residence time in a retention tank for the oxygen to react with and delignify the pulp. The oxygen also reacts with the organic solid in the black liquor resulting in a reduction of the heat value of the black liquor going to the recovery boiler. Additional reactions take place between the oxygen and sulfur compounds in the liquor, thus reducing or eliminating potential sources of total reduced sulfur (TRS) emissions by the pulp mill.
In the process, pulp slurry from the knotters with the black liquor still present and at a consistency of between 2 to 8% is transferred by a pump 30 through pipelines 10 and 40 to a steam mixer 50. Caustic, if needed may be added to the pulp slurry through side pipe 20 to maintain the pH of the pulp slurry between 11 and 12. At the steam mixer, steam is added to the pulp slurry through pipe line 130 to bring the temperature of the slurry to between 90 and 110° C before it flows into the efficient mixing device which could be a cavitation, type reactor 70 through line 60. Oxygen containing gas is introduced through a side inlet 140 and enters the efficient mixing device with the pulp slurry stream.
The pulp slurry and the oxygen containing gas are brought into intimate contact by the shearing and cavitation and mechanical forces generated as the rotor rotates at a high speed in the mixing device 70. The contacting is performed under suitable conditions of temperature and pressure whereby the oxygen begins to react with the lignin under caustic conditions to effect delignification. The reaction mixture proceeds through pipe line 80 into a retention tank 90 where under conditions of temperature, pressure and time the delignification reaction is continued further.
In order for the reaction to proceed as mentioned above, an oxygen containing gas must be used. Preferably oxygen with a minimum purity of 93% is employed. The preferred total reaction pressure should be not less than 80 psig and more preferably above 90 psig. The preferred minimum reaction temperature is 90° C but could be as high as 110° C.
The residence time of the reaction mixture in the retention tank is not less than 10 minutes but preferably up to 30 minutes. The reaction mixture is vVithdrawn through outlet 100 into a blow tank or gas-liquid separator 110 where reaction gases and unused oxygen gas disengages from the liquid product and is scrubbed and vented. The pulp sl~srry is withdrawn through line 120 and sent to the washing stage of the bleach line of the pulp and papermaking process.
By practicing the methods of the present invention, bleaching can be done with much less capital, specifically by not having to build, own, operate and maintain separate pressure towers for traditional oxygen delignification.
Un-oxidized white liquor can be used as the source of caustic as the oxidation of the white liquor also takes place in the mixer. Also, the exothermic heat of reaction of oxidation of white liquor raises the temperature of the pulp resulting in steam savings for oxygen delignification and most of the oxygen delignification reactions can be done at the existing pulp temperature.
Oxygen delignification before the brown stock washers lowers the BTU
value of the black liquor allowing for increased capacity of steam limited recovery boilers. Additionally, less oxidized white liquor will be needed in this sequence than traditional two stage oxygen delignification thus taking the load off the lime kiln and other white liquor systems.
The black liquor produced will have a lower viscosity because of the reaction of the oxygen with the Na2S and a portion of the dissolved lignin allowing for a higher percentage solids firing in the recovery boiler.
Methanal and other alcohols present in the black liquor before the brown stock washers will react to form a reducing environment in the pulp. With the availability of hydrogen limited, the side reactions that hurt pulp strength will also be limited.
Indeed pulp strength may increase.
The following is an example of a practice of the invention in accordance with the embodiment illustrated in FIG 1. In this example a side stream of softwood slurry at a consistency of 2.5°fo and containing residual black liquor was withdrawn with a Gould's pump 30 at a flow rate of 50 gallons per minute (gpm) through a side pipe 10 on the stock line going from the knotters to the first brown stock (BS) washers. The pH of the slurry was above 11.5 and so no additional caustic was added. Slurry temperature was 87° C. The slurry was heated to 90° C adding low-pressure steam through pipe 130 and mixed into the slurry with the steam mixer 50. Pure oxygen was added to the slurry through a side pipe 140 at a rate of 60 pounds per hour before it entered a high efficiency gas-liquid mixer9 in this case a controlled cavitation reactor 70. The slurry and gas were mixed for a few seconds at about 90 pounds per square inch (psi) in the reactor 70, the stock was transferred into a retention tank 90 and kept for 10 minutes and was finally returned to the bleach line just before the first BS washer. The pulp Kappa #
is the amount of lignin in the pulp sample. Samples were taken from the exit slurry stream for analysis. The following results were obtained:
Table 1 Inlet Outlet _ % Reduction ~
__ __ 16.5 37 Pul Ka a #~ 25.8 ~
Na2S, mglkg 21000 <200 ( non detect)almost 100 solids Dissolved Lignin,32.1 29.1 9.3 As % solids Comparatively, for conventional single stage oxygen delignification systems operating under similar conditions of temperature and pressure on a 10% consistency pulp, residence times of 40 minutes and higher will be required to achieve the 37% delignification.
While this invention has been described with respect to particular embodiments thereof, it is apparent that numerous other forms and modifications of this invention will be obvious to those skilled in the art.
The appended claims and this invention generally should be construed to cover all such obvious forms and modifications which are within the true spirit and scope of the present invention.
Un-oxidized white liquor can be used as the source of caustic as the oxidation of the white liquor also takes place in the mixer. Also, the exothermic heat of reaction of oxidation of white liquor raises the temperature of the pulp resulting in steam savings for oxygen delignification and most of the oxygen delignification reactions can be done at the existing pulp temperature.
Oxygen delignification before the brown stock washers lowers the BTU
value of the black liquor allowing for increased capacity of steam limited recovery boilers. Additionally, less oxidized white liquor will be needed in this sequence than traditional two stage oxygen delignification thus taking the load off the lime kiln and other white liquor systems.
The black liquor produced will have a lower viscosity because of the reaction of the oxygen with the Na2S and a portion of the dissolved lignin allowing for a higher percentage solids firing in the recovery boiler.
Methanal and other alcohols present in the black liquor before the brown stock washers will react to form a reducing environment in the pulp. With the availability of hydrogen limited, the side reactions that hurt pulp strength will also be limited.
Indeed pulp strength may increase.
The following is an example of a practice of the invention in accordance with the embodiment illustrated in FIG 1. In this example a side stream of softwood slurry at a consistency of 2.5°fo and containing residual black liquor was withdrawn with a Gould's pump 30 at a flow rate of 50 gallons per minute (gpm) through a side pipe 10 on the stock line going from the knotters to the first brown stock (BS) washers. The pH of the slurry was above 11.5 and so no additional caustic was added. Slurry temperature was 87° C. The slurry was heated to 90° C adding low-pressure steam through pipe 130 and mixed into the slurry with the steam mixer 50. Pure oxygen was added to the slurry through a side pipe 140 at a rate of 60 pounds per hour before it entered a high efficiency gas-liquid mixer9 in this case a controlled cavitation reactor 70. The slurry and gas were mixed for a few seconds at about 90 pounds per square inch (psi) in the reactor 70, the stock was transferred into a retention tank 90 and kept for 10 minutes and was finally returned to the bleach line just before the first BS washer. The pulp Kappa #
is the amount of lignin in the pulp sample. Samples were taken from the exit slurry stream for analysis. The following results were obtained:
Table 1 Inlet Outlet _ % Reduction ~
__ __ 16.5 37 Pul Ka a #~ 25.8 ~
Na2S, mglkg 21000 <200 ( non detect)almost 100 solids Dissolved Lignin,32.1 29.1 9.3 As % solids Comparatively, for conventional single stage oxygen delignification systems operating under similar conditions of temperature and pressure on a 10% consistency pulp, residence times of 40 minutes and higher will be required to achieve the 37% delignification.
While this invention has been described with respect to particular embodiments thereof, it is apparent that numerous other forms and modifications of this invention will be obvious to those skilled in the art.
The appended claims and this invention generally should be construed to cover all such obvious forms and modifications which are within the true spirit and scope of the present invention.
Claims (22)
1. A method for delignifying pulp in a slurry at low consistency from a fiber line of a papermaking system comprising adding oxygen to said slurry and mixing said slurry under conditions of temperature and pressure whereby said oxygen reacts with the lignin present in said pulp.
2. The method as claimed in claim 1 wherein the temperature of said slurry is about 85° C to about 120° C.
3. The method as claimed in claim 1 wherein the pressure of said mixing is about 20 to about 160 psig.
4. The method as claimed in claim 1 wherein said mixing occurs for up to 2 minutes.
5. The method as claimed in claim 1 wherein said pulp slurry contains black liquor.
6. The method as claimed in claim 1 wherein said mixing occurs in a gas liquid mixer.
7. The method as claimed in claim 6 wherein said mixer is a controlled cavitation device.
8. The method as claimed in claim 6 wherein said mixer further comprises a residence tank.
9. The method as claimed in claim 1 wherein said treated slurry is returned to said bleach line.
10 10. The method as claimed in claim 1 wherein said pulp slurry is drawn from said fiber line from a point selected from the group consisting of after the knotters and before the brown stock washers; after the digester and before the brown stock washers; and between any two stages of a multi-stage brownstock washing step.
11. A method for delignifying pulp slurry from a papermaking process fiber line comprising the steps:
a) directing said slurry to a mixing device;
b) adding oxygen to said slurry;
c) mixing said slurry and oxygen under temperature and pressure conditions to cause delignification;
d) directing said delignified reaction mixture to a holding tank; and e) directing said delignified reaction mixture to said papermaking process.
a) directing said slurry to a mixing device;
b) adding oxygen to said slurry;
c) mixing said slurry and oxygen under temperature and pressure conditions to cause delignification;
d) directing said delignified reaction mixture to a holding tank; and e) directing said delignified reaction mixture to said papermaking process.
12. The method as claimed in claim 11 wherein said pulp slurry is drawn from said fiber line from a point selected from the group consisting of after the knotters and before the brown stock washers; after the digester and before the brown stock washers; and between any two stages of a multi-step brownstock washing step.
13. The method as claimed in claim 11 further comprising adding caustic to said slurry.
14. The method as claimed in claim 11 further comprising adding steam to said slurry.
15. The method as claimed in claim 11 wherein said pulp slurry contains about 2 to about 8% by weight pulp.
16. The method as claimed in claim 11 wherein the pH of said pulp slurry is about at least 11.
17. The method as claimed in claim 11 wherein the temperature of said pulp slurry is about 85 to about 120° C.
18. The method as claimed in claim 11 wherein said mixing is at a pressure of about 20 to about 160 psig for up to 2 minutes.
19. The method as claimed in claim 11 wherein said pulp slurry is maintained at a pressure of about 20 to about 160 psig for about 5 to about 30 minutes in said holding tank.
20. The method as claimed in claim 11 wherein said pulp slurry contains black liquor.
21. The method as claimed in claims 20 further comprising reacting the Na2S in said black liquor with oxygen.
22. The method as claimed in claim 21 wherein said oxygen reacts with lignin present in said black liquor.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US51494603P | 2003-10-28 | 2003-10-28 | |
US60/514,946 | 2003-10-28 | ||
US10/898,101 | 2004-07-23 | ||
US10/898,101 US20050087315A1 (en) | 2003-10-28 | 2004-07-23 | Low consistency oxygen delignification process |
Publications (1)
Publication Number | Publication Date |
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CA2484557A1 true CA2484557A1 (en) | 2005-04-28 |
Family
ID=34426326
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CA002484557A Abandoned CA2484557A1 (en) | 2003-10-28 | 2004-10-13 | Low consistency oxygen delignification process |
Country Status (4)
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US (1) | US20050087315A1 (en) |
EP (1) | EP1528149A1 (en) |
AU (1) | AU2004222766A1 (en) |
CA (1) | CA2484557A1 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050150618A1 (en) * | 2000-05-17 | 2005-07-14 | Bijan Kazem | Methods of processing lignocellulosic pulp with cavitation |
US20050067122A1 (en) * | 2000-05-17 | 2005-03-31 | Bijan Kazem | Methods of processing lignocellulosic pulp with cavitation |
US7507014B1 (en) | 2005-08-05 | 2009-03-24 | Hydro Dynamics, Inc. | Controlled cavitation device with easy disassembly and cleaning |
US20080167204A1 (en) * | 2007-01-09 | 2008-07-10 | Billy Ray Slabaugh | Process for Enhancing Fluid Hydration |
US20080268302A1 (en) * | 2007-01-17 | 2008-10-30 | Mccall Joe | Energy production systems and methods |
WO2008089321A2 (en) * | 2007-01-17 | 2008-07-24 | Joe Mccall | Apparatus and methods for production of biodiesel |
US20160002858A1 (en) * | 2014-07-03 | 2016-01-07 | Linde Aktiengesellschaft | Methods for the oxygen-based delignification of pulp |
DE102020002445A1 (en) | 2020-04-23 | 2021-10-28 | Messer Austria Gmbh | Method and device for the production of bleached pulp |
IL297704A (en) | 2020-04-30 | 2022-12-01 | Hydro Dynamics Inc | System and method for treatment of plants for synthesis of compounds therefrom |
Family Cites Families (28)
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US3832273A (en) * | 1972-05-15 | 1974-08-27 | Carborundum Co | Composite refractory articles |
FI48764C (en) * | 1973-05-30 | 1977-07-26 | Ahlstroem Oy | Method and apparatus for bleaching cellulose pulp with molecular weight. |
US3951733A (en) * | 1974-11-06 | 1976-04-20 | International Paper Company | Delignification and bleaching of wood pulp with oxygen |
US4198266A (en) * | 1977-10-12 | 1980-04-15 | Airco, Inc. | Oxygen delignification of wood pulp |
US4248662A (en) * | 1979-01-22 | 1981-02-03 | The Black Clawson Company | Oxygen pulping with recycled liquor |
US4295926A (en) * | 1979-06-15 | 1981-10-20 | Weyerhaeuser Company | Method and apparatus for treating pulp with oxygen |
US4294654A (en) * | 1980-03-21 | 1981-10-13 | International Paper Company | Delignification and bleaching of lignocellulosic pulp via photo-oxygenation |
CA1186106A (en) * | 1981-11-02 | 1985-04-30 | Edward F. Elton | Process and apparatus for the oxygen delignification of pulp |
AT380496B (en) * | 1984-06-27 | 1986-05-26 | Steyrermuehl Papier | METHOD AND REACTOR FOR DELIGNIFYING CELLULAR WITH OXYGEN |
DE3428352A1 (en) * | 1984-08-01 | 1986-02-13 | Degussa Ag, 6000 Frankfurt | METHOD FOR DELIGNIFICATION AND BLEACHING OF CELLULAS |
NO872836L (en) * | 1987-02-12 | 1988-08-15 | Sigurd Fongen | PRESSURE DEVICING PRESSURE FOR FIBER SUSPENSIONS. |
SE465730C (en) * | 1988-03-17 | 2001-10-08 | Kvaerner Pulping Tech | Procedure for delignification of fibrous cellulose pulp |
NO882815L (en) * | 1988-06-24 | 1989-12-27 | Sigurd Fongen | PROCEDURE FOR CELLULOUS PREPARATION AND DELIGNIFICATION, WHEATING, DE-INKING AND CLEANING OF CELLULOSE FIBER AND DEVICE FOR CARRYING OUT THE PROCEDURE. |
US4946556A (en) * | 1989-04-25 | 1990-08-07 | Kamyr, Inc. | Method of oxygen delignifying wood pulp with between stage washing |
US5352332A (en) * | 1991-01-28 | 1994-10-04 | Maples Gerald E | Process for recycling bleach plant filtrate |
FI92725C (en) * | 1991-09-09 | 1994-12-27 | Ahlstroem Oy | Method for making cooking liquor |
US5690786A (en) * | 1991-11-26 | 1997-11-25 | Air Products And Chemicals Inc. | Process for the treatment of pulp with oxygen and steam using ejectors |
US5460696A (en) * | 1993-08-12 | 1995-10-24 | The Boc Group, Inc. | Oxygen delignification method incorporating wood pulp mixing apparatus |
US5439556A (en) * | 1993-08-16 | 1995-08-08 | The Boc Group, Inc. | Oxidation of white liquor using a packing column |
FR2719854B1 (en) * | 1994-05-11 | 1996-06-21 | Atochem Elf Sa | Process for the preparation of delignified and bleached chemical paper pulps. |
US6514380B1 (en) * | 1995-03-08 | 2003-02-04 | Andritz Oy | Treatment of chemical pulp |
SE505141C2 (en) * | 1995-10-23 | 1997-06-30 | Sunds Defibrator Ind Ab | Oxygen delignification of pulp in two stages with high loading of alkali and oxygen and temperature below 90 C in the first step |
US6319357B1 (en) * | 1995-10-23 | 2001-11-20 | Valmet Fibertech Aktiebolag | Method for two-stage oxygen bleaching and delignification of chemical pulp |
US20050067122A1 (en) * | 2000-05-17 | 2005-03-31 | Bijan Kazem | Methods of processing lignocellulosic pulp with cavitation |
US20050150618A1 (en) * | 2000-05-17 | 2005-07-14 | Bijan Kazem | Methods of processing lignocellulosic pulp with cavitation |
US6627784B2 (en) * | 2000-05-17 | 2003-09-30 | Hydro Dynamics, Inc. | Highly efficient method of mixing dissimilar fluids using mechanically induced cavitation |
CA2526333C (en) * | 2003-05-19 | 2011-12-06 | Hydro Dynamics, Inc. | Method and apparatus for conducting a chemical reaction in the presence of cavitation and an electrical current |
WO2005021050A1 (en) * | 2003-08-22 | 2005-03-10 | Hydro Dynamics, Inc. | Method and apparatus for irradiating fluids |
-
2004
- 2004-07-23 US US10/898,101 patent/US20050087315A1/en not_active Abandoned
- 2004-10-13 CA CA002484557A patent/CA2484557A1/en not_active Abandoned
- 2004-10-20 AU AU2004222766A patent/AU2004222766A1/en not_active Abandoned
- 2004-10-22 EP EP04256503A patent/EP1528149A1/en not_active Withdrawn
Also Published As
Publication number | Publication date |
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US20050087315A1 (en) | 2005-04-28 |
EP1528149A1 (en) | 2005-05-04 |
AU2004222766A1 (en) | 2005-05-12 |
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