Recovery of chlorine dioxide from gas streams

Information

  • Patent Grant
  • 6322768
  • Patent Number
    6,322,768
  • Date Filed
    Tuesday, October 13, 1998
    26 years ago
  • Date Issued
    Tuesday, November 27, 2001
    23 years ago
Abstract
A method for recovering chlorine dioxide from a gas. The method involves contacting gas containing chlorine dioxide with an alkaline metal base and peroxide to form an alkaline metal chlorite solution, and oxidizing the alkaline metal chlorite solution to generate chlorine dioxide.
Description




FIELD OF THE INVENTION




This invention relates to a method for recovering chlorine dioxide from gases, such as those that are vented in a plant that uses chlorine dioxide as a bleaching agent.




BACKGROUND OF THE INVENTION




Chlorine dioxide has been commonly used for bleaching pulp since the late 1950s. The process is referred to as the “D” stage of a pulp bleach plant and involves reacting pulp in water with bubbles of chlorine dioxide gas. This causes highly selective destruction of lignin without significant accompanying degradation of cellulose or hemicellulose. The strength of the pulp is preserved, while the pulp is stably brightened. Such bleaching of pulp is described in the following references: The Bleaching of Pulp (Rudra P. Singh, Ed. Tappi Press, 3


rd


ed. 1991); Gary A. Smook, Handbook for Pulp & Paper Technologists (Angus Wilde Publications, 2d ed., 1992); Christopher J. Biermann, Handbook of Pulping and Papermaking (Academic Press, 2d ed., 1996); Sven A Rydholm, Pulping Processes (Robert E. Krieger Publishing Co. 1985).




However, part of the chlorine dioxide that is used in the bleaching process becomes entrained in vent gas that is recovered from various locations in the bleach plant. Since chlorine dioxide is an environmental contaminant whose release is subject to regulatory limitations, it must be removed from the vent gas. This is normally accomplished using a scrubber that employs compounds or solutions that destroy the gaseous chlorine dioxide. Suitable chemicals for destroying chlorine dioxide gas include each of sodium thiosulfate, sulfur dioxide, caustic solution, and sulfide. For example, as described in U.S. Pat. No. 5,326,546, chlorine dioxide gas can be removed from a gas stream using a scrubbing solution containing sodium thiosulfate and an inorganic base, such as sodium hydroxide.




Such chemical treatment, however, is expensive. Furthermore, chlorine dioxide that is destroyed in vent gas must be replaced in the D stage of the bleaching operation.




There is therefore a need for a method that avoids loss of chlorine dioxide in vent gas generated in a bleaching operation, and minimizes the need for expensive scrubbing chemicals.




SUMMARY OF THE INVENTION




In one embodiment, the invention relates to a method for recovering chlorine dioxide from a gas stream which involves the steps of:




a) contacting the chlorine dioxide in the gas stream with an alkaline metal base and peroxide to form an alkaline metal chlorite solution; and




b) oxidizing the alkaline metal chlorite solution to generate chlorine dioxide.




In another embodiment, the invention relates to a method for scrubbing chlorine dioxide from bleach plant vent gas involving contacting the chlorine dioxide with alkaline metal base and peroxide in a vent gas scrubber to form alkaline metal chlorite solution, and removing the alkaline metal chlorite solution from the scrubber.











BRIEF DESCRIPTION OF THE DRAWING





FIG. 1

is a flow chart depicting scrubbing of vent gas containing chlorine dioxide to produce alkaline metal chlorite solution, and introduction of the alkaline metal chlorite solution into the bleach plant D stage to regenerate chlorine dioxide.











DETAILED DESCRIPTION OF THE INVENTION




All patents, patent applications, and publications cited herein are hereby incorporated by reference.




The present invention allows chlorine dioxide to be recovered from bleach plant gases, producing a substantial cost savings resulting from a reduced need for chlorine dioxide in the D stage of the bleach plant. Furthermore, the invention avoids use of expensive scrubbing chemicals that would otherwise be required to remove the chlorine dioxide from the vent gas. The invention also avoids possible release of environmentally harmful emissions, such as those containing sulfur.




According to the invention, chlorine dioxide that is entrained in a gas, such as vent gas from a bleach plant, is contacted with an alkaline metal base and peroxide to form an alkaline metal chlorite solution. This process normally takes place in a scrubber at a pH greater than 10, and an oxidation reduction potential (ORP) of less than 100. The alkaline metal chlorite solution is then oxidized to form chlorine dioxide, preferably by introduction into the D stage of the pulp bleaching process.




In a preferred embodiment of the invention, the following chemical process takes place:






ClO


2


+NaOH+1/2H


2


O


2


→NaClO


2


+H


2


O+1/2O


2


  (1)








5/4NaClO


2


+1/2H


2


SO


4


→ClO


2


+1/2H


2


O+NaSO


4


+1/4 NaCl.  (2)






In this embodiment, sodium hydroxide is employed as the alkaline metal base, and reaction (1) occurs in a scrubbing apparatus. For example, the sodium hydroxide can be introduced as a 20% solution in combination with a 5% peroxide solution in liquid that is introduced into one or more scrubbers employed at a bleach plant. Sodium chlorite solution formed according to reaction (1) in the scrubber is then removed and added in reaction (2) so as to generate chlorine dioxide. For example, the sodium chlorite solution can be introduced at a point of suction of a D stage mixer that combines pulp with chlorine dioxide, wherein the chlorine dioxide contacts sulfuric acid in the bleaching solution, and generates chlorine dioxide according to the reaction shown.




It is, however, possible, according to the invention, to contact the alkaline metal chlorite solution with acid in any manner that forms chlorine dioxide. For example, the chlorite solution can be added to the pulp before, or after, the pulp enters a pulp/chlorine dioxide mixer. Preferably, however, the chlorite solution is added at a point in the process such that it is well mixed with the acid. It is also possible, according to the invention, to recover alkaline metal chlorite solution from chlorine dioxide generated outside the bleach plant, and add the chlorite solution to the D stage. The invention also encompasses obtaining chlorite solution from a bleach plant scrubber, and oxidizing the chlorite outside of the D stage to generate chlorine dioxide. Preferably, both the scrubbing to obtain chlorite solution and the oxidation of chlorite solution occur at the bleach plant.




Any suitable acid can be employed in the reaction with alkaline metal chlorite solution to regenerate chlorine dioxide, including, without limitation, sulfuric acid, hydrochloric acid, and nitric acid.




Suitable alkaline metal bases for contacting with the chlorine dioxide gas in the scrubber include, without limitation, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium monoxide, and potassium monoxide. Sodium hydroxide is preferred.




It is also possible, according to the invention, to add the alkaline metal chlorite solution, e.g, sodium chlorite solution, in a bleaching solution of the D stage wherein the chlorite contacts chlorine that has been added to the bleaching stage. In this embodiment, for example, chlorine dioxide can be formed according to the following reaction:






NaClO


2


+Cl


2


→ClO


2


+NaCl







FIG. 1

is flow chart depicting a typical arrangement for removing chlorine dioxide from bleach plant gases according to the invention, and regenerating it in the bleach plant D stage. Caustic


1


and peroxide


3


are fed into a scrubber for vent gases


5


that are released from the bleach plant. These gases include chlorine dioxide, such as that which may be released from a chlorine dioxide generator, chlorine dioxide storage units, or chlorine dioxide sewers.




These chlorine dioxide containing gases are contacted in the scrubber with a solution containing the caustic and peroxide. The solution is recirculated counter-currently to the gases in a packed particle column.




The caustic


1


is generally in a concentration of 0.1 to 50%, preferably between about 5 and 25%, and most preferably about 20%. The peroxide


3


is generally in a concentration of 0.1 to 20%, preferably between about 2 and 10%, and most preferably about 5%.




The gases released from the plant


9


have sufficient chlorine dioxide removed from them to meet appropriate regulatory standards. Preferably more than 95% of the chorine dioxide is removed, most preferably more than about 99%, by the method of the invention.




While the method of the invention is intended to remove chlorine dioxide from vent gases in amounts that render the vent gas environmentally safe, the scrubber is preferably supplied with a backup system


19


of scrubbing chemicals that can be used as an alternate, or additional, means of removing the chlorine dioxide. For example, sodium thiosulfate, weak wash, white liquor, or SO


2


solution, can be employed in a conventional scrubbing reaction.




Sodium chlorite solution is removed from the scrubber through line


7


and maintained in a storage tank, from which it can be pumped to the D stage of the bleaching process. The sodium chlorite solution is brought through line


11


to the D stage mixer, to which is also fed pulp


13


and a mixture of chlorine dioxide and sulfuric acid


15


. The chlorite solution can be added at any part of the D stage but is preferably added at the D


0


stage, which has a lower pH than later D stages. Preferably the chlorite solution is contacted with the sulfuric acid at a pH lower than 3.0, and most preferably about 2.5. The chlorite solution contained in the mixture


17


is oxidized to form chlorine dioxide.




The following Example is intended to illustrate the invention, and not to be construed as limiting its scope.




EXAMPLE




The method of the invention was employed in a bleach plant that used two scrubbers for removal of chlorine dioxide from bleach plant vent gases. The scrubbers had previously employed a 20% solution of sodium hydroxide and a 30% solution of sodium thiosulfate as scrubbing chemicals at total flow rates to the two scrubbers of 1.5 gallon per minute (gpm) of the sodium hydroxide solution and 6 gpm of the sodium thiosulfate solution. These solutions were replaced with a 20% solution of sodium hydroxide and a 5% solution of peroxide fed at total flow rates to the two scrubbers of 4 gpm of the sodium hydroxide solution and 3 gpm of the hydrogen peroxide solution, in combination with 2 gpm of water.




Use of the sodium hydroxide and peroxide combination was found to result in a decrease in chlorine dioxide in the scrubber input and output gases of from 84 lbs./hr. to 0.1 lbs./hr. in one scrubber (i.e., more than 99% removal from the vent gas), and from 37 lbs./hr. to 1.6 lbs./hr. in the other scrubber (i.e., more than 95% removal from the vent gas). These levels were acceptable under the appropriate regulatory standards, and were comparable to those achieved using the conventional chemicals. The cost of scrubbing with sodium hydroxide and peroxide was substantially lower than the cost of using the conventional scrubbing chemicals.




The sodium chlorite solution formed in the scrubbers was removed and brought to a storage tank, from which it was pumped to the pulp/chlorine dioxide mixer for the D


0


stage of the bleach plant at a rate of less than 10 gpm. Sulfuric acid was fed to the D


0


stage in a density of about 72 lbs./cubic ft. as required to obtain a pH of about 2.3. Chlorine dioxide was fed to the D


0


stage at a rate sufficient to obtain a concentration of between 1 and 2% based on bone dry weight of the brown stock fed to the D


0


stage, as required to adequately bleach the brown stock.




Samples of the sodium chlorite solution were recovered and tested to determine the concentration of the chlorine dioxide solution generated in the D


0


stage. Chlorine dioxide was found to be present in concentrations varying from 4.5 to 5.5 g/l. While this was more dilute than the approximately 8 to 8.5 g/l concentration of “virgin liquor” chlorine dioxide conventionally used, it was adequate for bleaching pulp. The method of the invention was estimated to be capable of suppling about 1000 lbs. of the 32,000 lbs./day of ClO


2


used in the D stage of the plant.




This experiment demonstrated that the method of the invention successfully uses inexpensive scrubbing chemicals to remove chlorine dioxide from bleach plant vent gas, and recovers chlorine dioxide for use in the D stage of the bleach plant.



Claims
  • 1. In a method for recovering chlorine dioxide entrained in vent gas from a cellulose pulp bleaching process employing chlorine dioxide as a bleaching agent, the improvement comprising:a) contacting a chlorine dioxide containing gas vented from a cellulose pulp bleaching process with an alkaline metal base and peroxide to form an alkaline metal chlorite solution; and b) oxidizing the alkaline metal chlorite solution with a mixture of chlorine dioxide and an acid in the presence of pulp to produce chlorine dioxide.
  • 2. The method of claim 1, wherein said alkaline metal base is an alkaline metal hydroxide.
  • 3. The method of claim 1, wherein said alkaline metal base is alkaline metal carbonate.
  • 4. The method of claim 1, wherein said alkaline metal base is selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium monoxide, and potassium monoxide.
  • 5. The method of claim 1, wherein the alkaline metal chlorite solution and the mixture of chlorine dioxide and the acid are reacted at a pH lower than 3.0.
  • 6. A method for recovering chlorine dioxide from bleach plant vent gas comprising:a) contacting bleach plant vent gas containing chlorine dioxide with an alkaline metal base and hydrogen peroxide in a bleach plant vent gas scrubber to form an alkaline metal chlorite solution; and b) contacting the alkaline metal chlorite solution with a mixture of chlorine dioxide and an acid in the presence of pulp to produce chlorine dioxide.
  • 7. The method of claim 6, wherein the acid is sulfuric acid.
  • 8. The method of claim 6 wherein the acid is selected from the group consisting of hydrochloric acid and nitric acid.
  • 9. The method of claim 6, wherein said alkaline metal base is sodium hydroxide.
  • 10. A method of claim 6, wherein the alkaline metal chlorite solution and the mixture of chlorine dioxide and the acid are reacted at a pH lower than 3.0.
  • 11. A method for scrubbing chlorine dioxide from bleach plant vent gas comprising:a) contacting chlorine dioxide in the bleach plant vent gas with alkaline metal base and peroxide in a vent gas scrubber to form an alkaline metal chlorite solution; b) removing the alkaline metal chlorite solution from the scrubber; and c) reacting the alkaline metal chlorite solution with a mixture of chlorine dioxide and an acid in the presence of the pulp.
  • 12. The method of claim 11, wherein said alkaline metal base is sodium hydroxide, and said alkaline metal chlorite solution comprises sodium chlorine.
  • 13. The method of claim 11, wherein the alkaline metal chlorite solution and the mixture of chlorine dioxide and the acid are reacted at a pH lower than 3.0.
Parent Case Info

This application claims priority under 35 U.S.C. §119 from provisional application Ser. No. 60/102,335, filed Sep. 29, 1998, entitled “Recovery of Chlorine Dioxide from Gas Streams”, which application is hereby incorporated by reference.

US Referenced Citations (71)
Number Name Date Kind
2036311 White Apr 1936
2036375 Vincent Aug 1936
2169066 Cunningham Aug 1939
2332180 Soule Oct 1943
2616783 Wagner Nov 1952
3450493 Du Bellay et al. Jun 1969
3619350 Marchfelder Nov 1971
3755068 Rapson Aug 1973
3789108 Rapson Jan 1974
3829557 Winfield Aug 1974
3925540 Hatherly Dec 1975
3929975 Winfield Dec 1975
4070233 Matsuura Jan 1978
4079123 Fuller et al. Mar 1978
4081520 Swindells et al. Mar 1978
4105751 Caillol Aug 1978
4129484 Larson Dec 1978
4145401 Swindells et al. Mar 1979
4154809 Swindells et al. May 1979
4156713 Fuller May 1979
4216195 Jaszka et al. Aug 1980
4234446 Ramras Nov 1980
4251502 Forster Feb 1981
4414193 Fredette et al. Nov 1983
4465658 Fredette Aug 1984
4473540 Fredette Sep 1984
4590057 Hicks May 1986
4618479 Santillie et al. Oct 1986
4627969 Fredette et al. Dec 1986
4678653 Norell et al. Jul 1987
4678654 Holmstrom et al. Jul 1987
4678655 Twardowski Jul 1987
4770868 Norell Sep 1988
4795535 Bolduc et al. Jan 1989
4795619 Lerner Jan 1989
4904461 Yant et al. Feb 1990
4931268 Fredette et al. Jun 1990
4938943 Norell Jul 1990
4961918 Norell et al. Oct 1990
4978517 Norell et al. Dec 1990
4986973 Svedin et al. Jan 1991
5002746 Norell Mar 1991
5061471 Sundblad et al. Oct 1991
5066477 Sell et al. Nov 1991
5091166 Engstrom et al. Feb 1992
5091167 Engstrom et al. Feb 1992
5093097 Engstrom Mar 1992
5143580 Basta et al. Sep 1992
5145660 Wicksrom Sep 1992
5149442 Engstrom et al. Sep 1992
5154910 Engstrom Oct 1992
5165910 Oikawa et al. Nov 1992
5174868 Lipsztajn et al. Dec 1992
5227031 Sundblad Jul 1993
5273733 Winters et al. Dec 1993
5284553 Lipsztajn et al. Feb 1994
5326546 Rosenblatt et al. Jul 1994
5364604 Spink et al. Nov 1994
5366714 Bigauskas Nov 1994
5380517 Sokol Jan 1995
5545389 Winters et al. Aug 1996
5565180 Spink Oct 1996
5565182 Sokol Oct 1996
5589031 Farnstrand et al. Dec 1996
5674466 Dahl et al. Oct 1997
5676920 Lipsztajn Oct 1997
5770171 Sundblad et al. Jun 1999
5792316 Tsai Aug 1998
5851374 Cowley et al. Dec 1998
5858322 Gray Jan 1999
5895638 Tenney Apr 1999
Foreign Referenced Citations (3)
Number Date Country
53-66892 Jun 1978 JP
63-8203 Jan 1988 JP
55-098965 Jul 1980 JP
Non-Patent Literature Citations (6)
Entry
Jacobson, “Encyclopedia of Chemical Reactions”, vol. II, pp. 687, 726, 1948 (no month).*
Translation of JP 55-98, 965, Jul. 1980.*
The Bleaching of Pulp (Rudra P. Singh, Ed. Tappi Press, 3rd ed. 1991, pp. 20-21, 305-306). (no month).
Gary A. Smook, Handbook for Pulp & Paper Technologists Angus Wilde Publications, 2d ed., 1992, pp. 178-179. (no month).
Christopher J. Biermann, Handbook of Pulping and Papermaking (Academic Press, 2d ed., 1996, pp. 129, 132-133, 381). (no month).
Sven A. Rydholm, Pulping Processes (Robert E. Krieger Publishing Co. 1985, pp. 972-987). no month.
Provisional Applications (1)
Number Date Country
60/102335 Sep 1998 US