CA2429908C - An electrolytic process for the generation of stable solutions of chlorine dioxide - Google Patents
An electrolytic process for the generation of stable solutions of chlorine dioxide Download PDFInfo
- Publication number
- CA2429908C CA2429908C CA2429908A CA2429908A CA2429908C CA 2429908 C CA2429908 C CA 2429908C CA 2429908 A CA2429908 A CA 2429908A CA 2429908 A CA2429908 A CA 2429908A CA 2429908 C CA2429908 C CA 2429908C
- Authority
- CA
- Canada
- Prior art keywords
- chlorine dioxide
- solution
- chlorite
- effluent
- sodium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/24—Halogens or compounds thereof
- C25B1/26—Chlorine; Compounds thereof
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/24—Halogens or compounds thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Water Treatment By Electricity Or Magnetism (AREA)
Abstract
Chlorine dioxide gas dissolved in water is produced by passing a solution of stabilized chlorine dioxide or a sodium chlorite solution, with or without added sodium chloride, through an electrolytic cell having an anode and cathode, in the absence of a semi-permeable membrane but in the presence of a buffer. An anolyte with a pH below 10 is produced so that disproportination of the ClO2 in not appreciable.
Description
An Electrolytic Process for the Generation of Stable Solutions of Chlorine Dioxide Field of Invention This invention relates to a method of preparing chlorine dioxide in an electrolytic flow reactor. In particular, it relates to a method of preparing a stable solution of chlorine dioxide which will not disproportionate into chlorate and chlorite ions.
BACKGROUND OF THE INVENTION
Description of the Prior Art Early attempts by Logan (U.S. Patent 2,163,793) to produce chlorine dioxide (C1O2) by the electrolysis of sodium chlorite solution containing sodium chloride gave a 72% conversion of the chlorite to chlorine dioxide. However, the solution leaving the electrolytic cell had a pH of 11-12 due to the following reactions:
Na+ + e- - Na Na + H2O - NaOH + H2 The sodium hydroxide was the cause of the very high pH, which in turn caused the rapid decrease in C1O2 concentration due to the following rapid, irreversible, disproportionation reaction:
BACKGROUND OF THE INVENTION
Description of the Prior Art Early attempts by Logan (U.S. Patent 2,163,793) to produce chlorine dioxide (C1O2) by the electrolysis of sodium chlorite solution containing sodium chloride gave a 72% conversion of the chlorite to chlorine dioxide. However, the solution leaving the electrolytic cell had a pH of 11-12 due to the following reactions:
Na+ + e- - Na Na + H2O - NaOH + H2 The sodium hydroxide was the cause of the very high pH, which in turn caused the rapid decrease in C1O2 concentration due to the following rapid, irreversible, disproportionation reaction:
2 C1O2 + 2 OH- - C1O3- + C1O2- + H2O
Hence, if one intended to use the solution resulting from the above electrolysis as a deodorizer or disinfectant, the solution is practically useless due to the rapid loss Of C102, concentration. Also, as shown in the above equation, the hydroxyl ion concentration tends to decrease thereby gradually lowering the pH of the disproportionating solution.
This deficiency has been overcome in various patents by using a semi-permeable membrane between the anode and cathode. The theory of this approach has been elucidated by Kascur in U.S.
Patent 5,084,149, filed 4/4/91.
The semi-permeable membrane separates the effluents from each electrode. The chlorine dioxide produced at the anode has a pH
of 2- 3. The sodium hydroxide produced at the cathode has a pH
of 12 - 13. The chlorine dioxide stream from the anode is very stable at that pH and useful as a deodorant or disinfectant.
However, it is very expensive to generate C1O2 using this system.
It is not cost effective for the small applications for which it was intended. This is due in part to the membrane cost and the membrane's sensitivity to divalent ions, the complicated design and cost of the cell and power supply, and the necessity to periodically dispose of the by-products, sodium hydroxide and hydrogen.
The industry had developed on-site chemical generators which use sodium chlorite and chlorine gas as reactants to produce chlorine dioxide by oxidation of the sodium chlorite. These generators are used in applications where large quantities of chlorine dioxide are required. However, the use of chlorine as a reactant has come into disfavor due to the hazards of storing large amounts of chlorine gas. It is possible to substitute a combination of sodium hypochlorite (NaOCl) and an acid as a feed for the on-site chemical generators. However, the cost of generating C1O2 is increased appreciably.
Another approach to the generation of chlorine dioxide is to react sodium chlorite (NaC1O2) with acid such as hydrochloric acid. However, this system has the disadvantage of slow reaction kinetics and more importantly, a theoretical yield of only 80% due to the conversion of 1 mole of sodium chlorite to sodium chloride according to the following equation:
NaC1O2 + 4 HC1 - 4 C1O2 + 5 NaCl + 2 H2 0 Japanese Patent 1866 (1956) claims the electrolysis of an equal mixture by weight of sodium chlorite and sodium chloride with a copper or nickel cathode and a graphite anode. The overall equation for this reaction is:
2 NaC1O2 + 2 NaCl + H2O -, 2 C102 + 2 NaOH + H2 + 2 NaCl The yield is 72%. The hydrogen, sodium chloride and sodium hydroxide by-products are in contact with the chlorine dioxide, which results in an almost instantaneous loss of the chlorine dioxide due to the disproportionation reaction shown above, which is caused by the high pH of the sodium hydroxide containing effluent which renders the stream useless as a disinfectant/deodorizer due to the rapid loss of chlorine dioxide.
Japanese Patent 2316 (1956) discloses an electrochemical reduction of chlorates to chlorine dioxide in four compartments separated by ion exchange membranes using a porous carbon anode and an iron cathode.
U.S. Patent 4,248,681 (issued February 3, 1981 to Sweeney) discloses an electrolytic process in two sealed compartments separated by a Nafion R membrane using salt as the feed. A
mixture of chlorine and chlorine dioxide is produced. Pure chlorine dioxide is never produced. British Patent No.714,828 (published Sept. 1, 1954) describes the electrolysis of a chlorite solution containing a water-soluble salt of an inorganic oxy-acid other than sulfuric acid.
Electrolysis of a chlorite solution containing a water-soluble metal sulfate is disclosed in U.S. Patent 2,717,237 (issued September 6, 1955 to Rempelin).
Control of the concentration of sodium chlorite in the anolyte at 0.8 - 5% by means of a photometer is disclosed in U.S. Patent No. 4,542,008 (issued September 17, 1985 to Capuano). A
permselective membrane and electrodes containing an electrochemically active coating are used.
A particularly complicated electrolytic system has been patented by Halox in U.S. Patents 5,419,816, 5,609,742 and 5,705,050.
Hence, if one intended to use the solution resulting from the above electrolysis as a deodorizer or disinfectant, the solution is practically useless due to the rapid loss Of C102, concentration. Also, as shown in the above equation, the hydroxyl ion concentration tends to decrease thereby gradually lowering the pH of the disproportionating solution.
This deficiency has been overcome in various patents by using a semi-permeable membrane between the anode and cathode. The theory of this approach has been elucidated by Kascur in U.S.
Patent 5,084,149, filed 4/4/91.
The semi-permeable membrane separates the effluents from each electrode. The chlorine dioxide produced at the anode has a pH
of 2- 3. The sodium hydroxide produced at the cathode has a pH
of 12 - 13. The chlorine dioxide stream from the anode is very stable at that pH and useful as a deodorant or disinfectant.
However, it is very expensive to generate C1O2 using this system.
It is not cost effective for the small applications for which it was intended. This is due in part to the membrane cost and the membrane's sensitivity to divalent ions, the complicated design and cost of the cell and power supply, and the necessity to periodically dispose of the by-products, sodium hydroxide and hydrogen.
The industry had developed on-site chemical generators which use sodium chlorite and chlorine gas as reactants to produce chlorine dioxide by oxidation of the sodium chlorite. These generators are used in applications where large quantities of chlorine dioxide are required. However, the use of chlorine as a reactant has come into disfavor due to the hazards of storing large amounts of chlorine gas. It is possible to substitute a combination of sodium hypochlorite (NaOCl) and an acid as a feed for the on-site chemical generators. However, the cost of generating C1O2 is increased appreciably.
Another approach to the generation of chlorine dioxide is to react sodium chlorite (NaC1O2) with acid such as hydrochloric acid. However, this system has the disadvantage of slow reaction kinetics and more importantly, a theoretical yield of only 80% due to the conversion of 1 mole of sodium chlorite to sodium chloride according to the following equation:
NaC1O2 + 4 HC1 - 4 C1O2 + 5 NaCl + 2 H2 0 Japanese Patent 1866 (1956) claims the electrolysis of an equal mixture by weight of sodium chlorite and sodium chloride with a copper or nickel cathode and a graphite anode. The overall equation for this reaction is:
2 NaC1O2 + 2 NaCl + H2O -, 2 C102 + 2 NaOH + H2 + 2 NaCl The yield is 72%. The hydrogen, sodium chloride and sodium hydroxide by-products are in contact with the chlorine dioxide, which results in an almost instantaneous loss of the chlorine dioxide due to the disproportionation reaction shown above, which is caused by the high pH of the sodium hydroxide containing effluent which renders the stream useless as a disinfectant/deodorizer due to the rapid loss of chlorine dioxide.
Japanese Patent 2316 (1956) discloses an electrochemical reduction of chlorates to chlorine dioxide in four compartments separated by ion exchange membranes using a porous carbon anode and an iron cathode.
U.S. Patent 4,248,681 (issued February 3, 1981 to Sweeney) discloses an electrolytic process in two sealed compartments separated by a Nafion R membrane using salt as the feed. A
mixture of chlorine and chlorine dioxide is produced. Pure chlorine dioxide is never produced. British Patent No.714,828 (published Sept. 1, 1954) describes the electrolysis of a chlorite solution containing a water-soluble salt of an inorganic oxy-acid other than sulfuric acid.
Electrolysis of a chlorite solution containing a water-soluble metal sulfate is disclosed in U.S. Patent 2,717,237 (issued September 6, 1955 to Rempelin).
Control of the concentration of sodium chlorite in the anolyte at 0.8 - 5% by means of a photometer is disclosed in U.S. Patent No. 4,542,008 (issued September 17, 1985 to Capuano). A
permselective membrane and electrodes containing an electrochemically active coating are used.
A particularly complicated electrolytic system has been patented by Halox in U.S. Patents 5,419,816, 5,609,742 and 5,705,050.
These patents describe a system in which the anode and cathode are separated by cation exchange membrane. In addition, the space between the anode and the cation exchange membrane is packed with a cation exchange resin, which must be replaced when spent. It is obvious that this cell is complicated and costly to construct and maintenance costs are high due to the need to replace the cation exchange membrane and cation exchange resin.
Also the unit has capacity limitations due to the packing and cell construction.
SUMMARY OF THE INVENTION
The present invention provides a simple, inexpensive system for the generation of chlorine dioxide, without membranes or ion-exchange resins. It comprises a pipe cell wherein stabilized chlorine dioxide or chlorite solution, used as the reactant, flows through the cell from bottom to top (up-flow) and where a buffer system is used to control the pH of the effluent.
More particularly, there is described an electrolytic process for generating a stable solution of chlorine dioxide, which process comprises the steps of:
a) preparing an aqueous solution containing chlorite ions in a concentration of about 10 to about 80,000 ppm;
b) adding at least one of a buffering agent and an acid to the aqueous chlorite solution in an amount sufficient to control the pH of the chlorine dioxide solution at a pH of about 9.5 or below after electrolysis;
c) up flowing the at least one of the buffered and acidified aqueous chlorite solution through an electrolytic cell containing an anode and a cathode, but no membrane, at a voltage of about 1 volt to about 12 volts to electrolyze the chlorite to chlorine dioxide and generate the stable solution of chlorine dioxide; and d) removing the stable solution of chlorine dioxide as the effluent from the top of the electrolytic cell.
The cathode consists of an outer stainless steel pipe. The anode consists of a carbon electrode or a dimensionally stable anode. The anode is positioned in the center of the pipe and insulated from the cathode. The power supply can be a DC source of 3-12 volts. A low cost D.C. power supply is adequate for this application.
The improvement in this system is the production of a continuous stream of chlorine dioxide gas dissolved in an aqueous solution at a pH below 10 due to the presence of the buffer. The resulting solution is stable and will not disproportionate on standing.
The electrolytic cell is shown in Figure 1. The outer wall of the cell comprises a metal pipe, such as a stainless steel pipe with tab 1 welded onto the surface to act as a connector for the electrical connection (cathode 2). The anode 3 is positioned in the center of the pipe and insulated from the cathode 2 by plastic caps 4 and 5 at both ends of the stainless steel pipe.
The anode 3 is either carbon plated with lead dioxide or a dimensionally stable anode (i.e., a metal such as titanium coated with a precious metal such as platinum, palladium, or iridium). The flow of liquid is into the bottom of the cell and out of the outlet 6 at the top of the vertically mounted pipe flow cell. A source of DC voltage is connected, negative to the cathode and positive to the anode. No membrane, asbestos barrier or resin bed is required in this simple cell design.
The electrolyte is a stabilized chlorine dioxide or a sodium chlorite solution having a concentration between 0.01 - 5.0 %
wt. of total available chlorine dioxide. A buffer such as NaH2PO4, is added to the electrolyte to control its conductivity and the pH of the resulting electrolyzed solution. Optionally, but preferably, 0.5-2.5% wt. of sodium chloride is added to impart further control to the conductivity of the electrolyte.
The mixture (i.e., electrolyte, buffer and optionally sodium chloride) is then passed through the cell at various flow rates and applied voltage to attain high conversions to C102.
The reactions occurring in this cell at the cathode are sodium ions acquiring an electron (e) and being reduced to sodium metal.
Na+ + e- -- Na The sodium metal then immediately reacts with water to produce sodium hydroxide and hydrogen as shown in equation below.
2Na + 2H20 --> 2NaOH + H2O
Chlorine is formed at the anode by the reaction:
2C1- - 2e- ~ C12 In the reaction at the anode the chlorite ion loses an electron to form chlorine dioxide as shown in the following equation:
C102- - e- -- C102 or chlorine immediately reacts with sodium chlorite to form chlorine dioxide plus sodium chloride as shown in the following DOCSTOR: 1922715\1 equation:
2 NaC102 + C12 --a. 2 C102 + 2 NaCl Another possible reaction in the electrolytic cell is the reduction of chlorate ion to chlorine dioxide in an acid medium by the following reaction:
NaC103 + 2 HC1 -, C102 + % C12 + H2O + NaCl The resulting chlorine then reacts with some of the sodium chlorite to form more C102 as follows:
2 NaC102 + C12 -> 2 C102 + 2 NaCl The key to producing a useful solution of chlorine dioxide from a pipe cell of the type shown in Figure I is to add a buffer to the electrolyte solution to control the pH of the effluent to a pH below 10, preferably in the pH range of 8-9, but possibly as low as 5. This is accomplished by the addition of various buffers which have the capacity to absorb appreciable amounts of hydroxyl ion and to prevent the pH from rising to a level which will allow the disproportionation reaction to take place. This is illustrated below.
H3 B03 + 3 NaOH -* Na3BO3 + 3H20 Likewise, phosphate, citrate, and carbonate buffers can be-used in the same manner, thusly:
NaH2PO4 + NaOH -> Na2HPO4 + H2O
Na2HPO4 + NaOH -3 Na3PO4 + H2O
or NaHCO3 + NaOH -, Na2CO3 + H2O
Citric acid, being a. tribasic acid reacts in the same manner, acting as a buffer.
Sufficient buffer is added to absorb all of the NaOH which can be generated by high, conversions of stabilized chlorine dioxide DOCSTOR: 1922715\1 sold under the Trade-marks - Anthium Dioxcide, Purogene Professional, Carnebon 200, Cryocide 20, Purogene or Oxine, or buffered chlorite to chlorine dioxide.
For example, in 2% stabilized chlorine dioxide, one would expect about 0.03 moles of NaOH per 100 grams of solution to be generated on electrolysis, requiring about 0.6 grams of boric acid to control the pH.
In like manner, the pipe cell will produce hypobromous acid from a feed of sodium bromide, sodium chloride and a buffer to control the final solution pH according to the following equations:
Na+ + e- - Na Na + H2O -3, NaOH + %H2 2C1- - 2e- -> C12 C12 + H2O - HOC1 + HC1 HOC1 + NaBr -, HOBr + NaCl Bromine generated from the electrolysis of bromide ion will react with water to produce additional HOBr. As in the case of sodium chlorite electrolysis, buffers are used to control the pH
of the effluent electrolyte, preferably in the range of pH 5 -9.
COMPARATIVE EXAMPLES
An electrolyte solution was prepared by mixing 9 grams of 80%
technical sodium chlorite, 22.5 grams of sodium chloride, and 3.0 liters, of water. This solution was passed through a Pepcon cell which has a lead oxide- stabilized graphite anode and a stainless steel cathode at a rate of 92 cc/min. A D.C. power source supplied 6 volts and the current was 6.4 amps. Under DOCSTOR: 1922715\1 these conditions, the cell produced 525 ppm of free chlorine dioxide from a total available chlorine dioxide content of 1,406 ppm at a pH of 11.7. The conversion of chlorite to chlorine dioxide was 37%. However, the effluent solution was useless for disinfection or odor control as shown by the fact that the color of the solution disappeared almost immediately indicating that the disproportionation reaction was taking place rapidly. Free chlorine dioxide is the molecular chlorine dioxide in the form of a water soluble yellow gas. Total available chlorine dioxide is the amount of free chlorine dioxide which could be generated from a given chlorite solution if it was all converted to C102.
Numerous other experiments were conducted under the same conditions, with essentially the same results, as shown in Table I.
For example, a solution made up by dissolving 3 grams of 80%
technical sodium chlorite and 15 grams of sodium chloride in 3 liters of water was passed through the Pepcon cell at 106 cc/min. The cell drew a current of 3.2-3.3 amps at 6 volts DC.
The total available chlorine dioxide before electrolysis was 564 ppm at a pH of 7.2. After electrolysis, the pH of the solution was 11.1, the free chlorine dioxide was 310 ppm and the total available chlorine dioxide was 430 ppm. This gave a conversion of 55% based on the original total available chlorine dioxide and 72% based on the total available chlorine dioxide available in the effluent from the cell. In 30 minutes the color had almost disappeared from the solution (20 ppm free) and the pH
had decreased to 8.48, indicating that the disproportionation reaction had occured.
Since the disproportionation reaction does not occur to any extent at lower pH, the cell was then operated with a solution designed to maintain the pH below 7-8. This approach is wherein the invention lies. Several systems should be considered for control of the effluent pH, namely potassium acid phthalate, boric acid, sodium bicarbonate, and sodium dihydrogen phosphate plus any other system capable of pH control. Examples of the use of each of these systems are given in Table I, Runs 14-18.
The pH of the effluents from these runs are in the range of 5-9.
No loss of chlorine dioxide was noted over time due to the disproportionation reaction. In addition, periodic removal of sodium hydroxide from the cathode was not required (as with the membrane cell) since the sodium hydroxide and hydrogen produced is in the pipe cell's effluent. In small cells the hydrogen production is not a problem but in larger cells it should be vented from the cell electrolyte.
Of course, a similar result can be obtained by omitting the buffers used in Runs 14-18 and then adjusting the pH of the effluent by adding acid but this adds an extra step to the process and requires complicated equipment to add acid to a controlled pH. Additionally, the disproportation reaction takes place until the pH is lowered, resulting in some loss of chlorine dioxide.
The electrolysis of a 2% stabilized chlorine dioxide is carried out by adding an appreciable quantity of a reagent (2 to 20 grams per liter, preferably 10 gpl) which is capable of forming a buffer with the ingredients of Carnebon 200TM, such boric acid, sodium dihydrogen phosphate, potassium acid phthalate, or sodium bicarbonate, etc. This solution is then passed through a Pepcon 20 amp. laboratory cell at the optimum rate of flow to give maximum conversion to free chlorine dioxide. The conversion is at least 60% and the pH of the resulting solution is below 10, preferably in the range of 8 - 9.
This pH range prevents the disproportionation of chlorine dioxide to chlorate and chlorite. The Pepcon cell has a lead oxide stabilized graphite anode and a stainless steel cathode.
The applied voltage can vary between 3 -12 volts D.C. The pipe cell is identical to the Pepcon cell except that the anode is a dimensionally stable anode as described above.
A less desirable alternative is to add acid or buffers to the effluent to reduce the pH from 11 - 12 down to 8 - 9, rather than including them in the cell feed. This approach will prevent the disproportionation reaction from proceeding, but there is some loss due to the speed of the reaction before the buffering takes effect.
Another alternative is to pass the effluent through an acid ion exchange resin to lower the pH of the solution to 8 - 9 to prevent the undesirable disproportination reaction from taking place. Another possible approach to pH control is dilution with neutral or acidic water.
EXAMPLES
Example 1.
A solution of Anthium Dioxcide , containing 50,000 ppm stabilized chlorine dioxide was run through the flow cell shown in Figure I
at a flow rate of about 50 cc/minute. The voltage was 6 volts and the current was 5 amperes. The Anthium Dioxcide contains a sodium carbonate - sodium bicarbonate buffer. The conversion was high, as evidenced by the dark orange color of the effluent.
The run was terminated immediately due to the high concentration of chlorine dioxide being generated and no quantitative data was determined for this run.
Example 2.
Carnebon 200 , which contains 20,000 ppm stabilized chlorine dioxide is run through the flow cell at a rate of 30 cc/minute, 6 volts and 4.8 amperes. The Carnebon 200 contains a sodium carbonate - bicarbonate buffer. It is further buffered by addition of 10 grams/liter of boric acid before the electrolysis. The effluent from the cell is diluted 3/1 with deionized water. The diluted stream should then contain about 3000 ppm free C1O2 and a have pH of 8.3. The solution is stable at this pH with no tendency to disproportionate.
Example 3.
The electrolysis is repeated under the conditions shown in Example 2 except that the boric acid buffer is omitted. The amperes observed in this example will be slightly reduced and on dilution the solution will have, only about 2500 ppm free 0102 and the pH should be about 8.9. The solution will not lose its yellow color, which would indicate disproporination and a decreased chlorine dioxide concentration.
Example 4.
Carnebon 200 is diluted 1/1 with deionized water to give a feed solution containing 10,000 ppm total available chlorine dioxide.
This solution is then passed through the flow cell of Figure 1 at a rate of 25 cc/minute, at 6 volts and 4.3 amperes. After electrolysis, the solution should be immediately diluted 1/1 with deionized water and should contain a Cl02 concentration of about 3000 ppm free C1O2 and have pH of 8.9. No decolorization of the solution should be observed on standing.
Example 5.
A solution of 1 gram per liter of sodium chlorite, 5 grams per liter of sodium chloride, and 2 grams per liter of potassium hydrogen phthalate (KHP) was prepared. This solution was passed through the electrolysis cell at a rate of 125 cc/min. at 6 volts, giving a current of 2.9 amps. The resulting undiluted solution had a free chlorine dioxide concentration of 350 ppm and a total available chlorine dioxide concentration giving an 85% conversion. The solution had a pH of 5.6, was stable and did not disproportionate to chlorite and chlorate.
Example 6.
The solution of Example 5. was passed through the same cell at a rate of 150 cc/min. and a current of 3 amperes. The resulting solution had a free chlorine dioxide content of 330 ppm and a total available chlorine dioxide content of 421 ppm for a conversion of 78%.
Example 7.
A solution of 1 gram per liter of sodium chlorite, 5 grams per liter of sodium chloride, and 2 grams per liter of boric acid was prepared. This solution was passed through the cell at a rate of 100 cc/min. at 6 volts and 2.6 amperes current. The effluent had a free chlorine dioxide content of 350 ppm and a total available chlorine dioxide content of 389 ppm for a conversion of 90%. The pH of the solution was 8.3. This solution showed no tendency to disproportionate.
Example 8.
A solution of 1 gram per liter of sodium chlorite, 5 grams per liter of sodium chloride, and 2 grams per liter of sodium bicarbonate was passed through the cell at a rate of 100 cc/min.
at 6 volts and 3 amperes current. The effluent from the cell had a pH of 8.9, a free chlorine dioxide content of 150 ppm and a total available chlorine dioxide content of 364 ppm for a conversion of 41%. The solution was stable in color.
Example 9.
A solution containing 1 gram per liter of sodium chlorite and 5 grams per liter of sodium chloride was electrolyzed at a feed rate of 106 cc/min. at 6 volts and 3.2 amperes. The effluent from the cell had a pH of 11.1, a free chlorine dioxide content of 310 ppm and a total available chlorine dioxide content of 430 ppm for a conversion of 72%. The high pH effluent began to immediately disproportionate to chlorite and chlorate. Very quickly this solution became colorless indicating complete loss of the free chlorine dioxide in solution.
Example 10.
Example 2 is repeated except that 10 grams per liter of sodium chloride is added to the Carnebon 200 stabilized chlorine dioxide solution before electrolysis. The electrolysis conditions are repeated exactly as in Example 2. After dilution with 3 parts water to 1 part of the cell effluent electrolyte should have 4000 ppm free chlorine dioxide and a pH of 8.3, with no tendency to disproportionate.
Example 11.
Example 9 is repeated using an eductor downstream from the cell.
Municipal water is supplied to the eductor and the effluent from the cell is fed into the throat of the eductor. The flow rates of the effluent stream and the municipal water stream are adjusted so that the final concentration of the free chlorine dioxide is 5 ppm. The pH of the total stream should be about 9.5 and the color of the solution should be stable. No appreciable disproportination should occur.
Example 12.
Example 11 is repeated but an acid or an acidic buffer is added to the throat of the eductor in an amount sufficient to give a pH in the range of 7 to 8.9. The color of the solution should be stable and should contain 5 ppm free chlorine dioxide and should show no decrease.
Example 13.
A solution containing 31,400 ppm of sodium chlorate is mixed 1:1 by volume with 20,000 ppm of stabilized chlorine dioxide, to provide a solution containing 15,704 ppm of sodium chlorate and 13,422 ppm of sodium chlorite. Two grams per liter of potassium acid phthalate is added to this solution. It is passed through a Pepcon cell at a rate of 150 cc/minute at a voltage of 6 volts and a current of about 4.5 amperes. When 1 part of the effluent from the cell is diluted with 4 parts water, the concentration of free (molecular) chlorine dioxide should be about 3000 ppm.
This indicates some reduction of the chlorate to chlorine dioxide as well as the oxidation of chlorite to chlorine dioxide in the same electrolytic cell.
Example 14.
A total of 60 parts of salt water obtained from the ocean (about 30,000 ppm sodium chloride) is mixed with 40 parts of 2%
stabilized chlorine dioxide to give a feed solution containing about 8,000 ppm total available chlorine dioxide and 18,000 ppm sodium chloride as a feed solution for a 5-5M Cloropac0 unit (Electrolytic Hypochlorite Generation Cell). This cell is designed, when operated at a feed rate of 20 gallons per minute to produce 0.5 lbs. per hour of sodium hypochlorite at a concentration of 50 ppm. The effluent from this cell should have a pH of about 8.9 and a free chlorine dioxide content of 500 ppm and 50ppm of sodium hypochlorite. After dilution, this solution can be used as an antimicrobial in the water used for cooling, ballast water, effluent sewage treatment and the main on-board seawater flow. The effluent from this cell can also be used in the condenser cooling in power plants and offshore oil drilling and production facilities to control marine growth.
Slower feed rates will tend to give higher conversions to chlorine dioxide and sodium hypochlorite. When seawater feed is used, it should be noted that additional buffer should be added to control the pH of the effluent in the presence of the generated sodium hypochlorite. If fresh water, containing no salt, is used to dilute the stabilized chlorine dioxide or neat stabilized chlorine dioxide alone is used as feed without the chloride, no additional buffer may be required and chlorine dioxide alone will result, with no co-produced sodium hypochlorite.
Example 15. A solution containing 5 grams/liter of sodium chlorite, 7.5 grams per liter of sodium chloride, and 10 grams per liter of sodium dihydrogen phosphate was passed through the pipe cell having a dimensionally stable center anode at a rate of 30 gallons per day at 12 volts and 20 amps. The temperature of the cell electrolyte was 12 degrees Centigrade and the pH was 6.2. The molecular chlorine dioxide content of the solution was 1252 ppm from a total available C1O2 content of 2197 ppm, giving a conversion of 57% (Run #5 in Table I). At this pH there was no tendency towards disproportionation of the chlorine dioxide to chlorate and chlorite.
Example 16. A solution containing 5.0 grams per liter of stabilized chlorine dioxide and 10 grams per liter of NaH2PO4 was electrolyzed through the same cell as in Example 15 at a rate of 17.5 ml per minute, giving a residence time of 13.1 minutes for the solution in the cell. The voltage was 12 and the current was 9 amps, giving a cell effluent having a pH of 5.9 and 720 ppm of free (molecular) 0102 from a solution having a total available C1O2 content for a 60.9% conversion. Again there was no loss of chlorine dioxide through disproportionation.
Example 17. A solution containing 6.0 grams per liter of sodium chloride, 1.0 gram per liter of sodium bromide and 2.0 grams of potassium hydrogen phthalate is passed through the pipe cell at a rate of 200 ml. per minute. The voltage in the cell was 12 volts and the current was 7.0 amps. The amount of HOBr produced in the solution was 1336 ppm at a pH of 5.7.
Also the unit has capacity limitations due to the packing and cell construction.
SUMMARY OF THE INVENTION
The present invention provides a simple, inexpensive system for the generation of chlorine dioxide, without membranes or ion-exchange resins. It comprises a pipe cell wherein stabilized chlorine dioxide or chlorite solution, used as the reactant, flows through the cell from bottom to top (up-flow) and where a buffer system is used to control the pH of the effluent.
More particularly, there is described an electrolytic process for generating a stable solution of chlorine dioxide, which process comprises the steps of:
a) preparing an aqueous solution containing chlorite ions in a concentration of about 10 to about 80,000 ppm;
b) adding at least one of a buffering agent and an acid to the aqueous chlorite solution in an amount sufficient to control the pH of the chlorine dioxide solution at a pH of about 9.5 or below after electrolysis;
c) up flowing the at least one of the buffered and acidified aqueous chlorite solution through an electrolytic cell containing an anode and a cathode, but no membrane, at a voltage of about 1 volt to about 12 volts to electrolyze the chlorite to chlorine dioxide and generate the stable solution of chlorine dioxide; and d) removing the stable solution of chlorine dioxide as the effluent from the top of the electrolytic cell.
The cathode consists of an outer stainless steel pipe. The anode consists of a carbon electrode or a dimensionally stable anode. The anode is positioned in the center of the pipe and insulated from the cathode. The power supply can be a DC source of 3-12 volts. A low cost D.C. power supply is adequate for this application.
The improvement in this system is the production of a continuous stream of chlorine dioxide gas dissolved in an aqueous solution at a pH below 10 due to the presence of the buffer. The resulting solution is stable and will not disproportionate on standing.
The electrolytic cell is shown in Figure 1. The outer wall of the cell comprises a metal pipe, such as a stainless steel pipe with tab 1 welded onto the surface to act as a connector for the electrical connection (cathode 2). The anode 3 is positioned in the center of the pipe and insulated from the cathode 2 by plastic caps 4 and 5 at both ends of the stainless steel pipe.
The anode 3 is either carbon plated with lead dioxide or a dimensionally stable anode (i.e., a metal such as titanium coated with a precious metal such as platinum, palladium, or iridium). The flow of liquid is into the bottom of the cell and out of the outlet 6 at the top of the vertically mounted pipe flow cell. A source of DC voltage is connected, negative to the cathode and positive to the anode. No membrane, asbestos barrier or resin bed is required in this simple cell design.
The electrolyte is a stabilized chlorine dioxide or a sodium chlorite solution having a concentration between 0.01 - 5.0 %
wt. of total available chlorine dioxide. A buffer such as NaH2PO4, is added to the electrolyte to control its conductivity and the pH of the resulting electrolyzed solution. Optionally, but preferably, 0.5-2.5% wt. of sodium chloride is added to impart further control to the conductivity of the electrolyte.
The mixture (i.e., electrolyte, buffer and optionally sodium chloride) is then passed through the cell at various flow rates and applied voltage to attain high conversions to C102.
The reactions occurring in this cell at the cathode are sodium ions acquiring an electron (e) and being reduced to sodium metal.
Na+ + e- -- Na The sodium metal then immediately reacts with water to produce sodium hydroxide and hydrogen as shown in equation below.
2Na + 2H20 --> 2NaOH + H2O
Chlorine is formed at the anode by the reaction:
2C1- - 2e- ~ C12 In the reaction at the anode the chlorite ion loses an electron to form chlorine dioxide as shown in the following equation:
C102- - e- -- C102 or chlorine immediately reacts with sodium chlorite to form chlorine dioxide plus sodium chloride as shown in the following DOCSTOR: 1922715\1 equation:
2 NaC102 + C12 --a. 2 C102 + 2 NaCl Another possible reaction in the electrolytic cell is the reduction of chlorate ion to chlorine dioxide in an acid medium by the following reaction:
NaC103 + 2 HC1 -, C102 + % C12 + H2O + NaCl The resulting chlorine then reacts with some of the sodium chlorite to form more C102 as follows:
2 NaC102 + C12 -> 2 C102 + 2 NaCl The key to producing a useful solution of chlorine dioxide from a pipe cell of the type shown in Figure I is to add a buffer to the electrolyte solution to control the pH of the effluent to a pH below 10, preferably in the pH range of 8-9, but possibly as low as 5. This is accomplished by the addition of various buffers which have the capacity to absorb appreciable amounts of hydroxyl ion and to prevent the pH from rising to a level which will allow the disproportionation reaction to take place. This is illustrated below.
H3 B03 + 3 NaOH -* Na3BO3 + 3H20 Likewise, phosphate, citrate, and carbonate buffers can be-used in the same manner, thusly:
NaH2PO4 + NaOH -> Na2HPO4 + H2O
Na2HPO4 + NaOH -3 Na3PO4 + H2O
or NaHCO3 + NaOH -, Na2CO3 + H2O
Citric acid, being a. tribasic acid reacts in the same manner, acting as a buffer.
Sufficient buffer is added to absorb all of the NaOH which can be generated by high, conversions of stabilized chlorine dioxide DOCSTOR: 1922715\1 sold under the Trade-marks - Anthium Dioxcide, Purogene Professional, Carnebon 200, Cryocide 20, Purogene or Oxine, or buffered chlorite to chlorine dioxide.
For example, in 2% stabilized chlorine dioxide, one would expect about 0.03 moles of NaOH per 100 grams of solution to be generated on electrolysis, requiring about 0.6 grams of boric acid to control the pH.
In like manner, the pipe cell will produce hypobromous acid from a feed of sodium bromide, sodium chloride and a buffer to control the final solution pH according to the following equations:
Na+ + e- - Na Na + H2O -3, NaOH + %H2 2C1- - 2e- -> C12 C12 + H2O - HOC1 + HC1 HOC1 + NaBr -, HOBr + NaCl Bromine generated from the electrolysis of bromide ion will react with water to produce additional HOBr. As in the case of sodium chlorite electrolysis, buffers are used to control the pH
of the effluent electrolyte, preferably in the range of pH 5 -9.
COMPARATIVE EXAMPLES
An electrolyte solution was prepared by mixing 9 grams of 80%
technical sodium chlorite, 22.5 grams of sodium chloride, and 3.0 liters, of water. This solution was passed through a Pepcon cell which has a lead oxide- stabilized graphite anode and a stainless steel cathode at a rate of 92 cc/min. A D.C. power source supplied 6 volts and the current was 6.4 amps. Under DOCSTOR: 1922715\1 these conditions, the cell produced 525 ppm of free chlorine dioxide from a total available chlorine dioxide content of 1,406 ppm at a pH of 11.7. The conversion of chlorite to chlorine dioxide was 37%. However, the effluent solution was useless for disinfection or odor control as shown by the fact that the color of the solution disappeared almost immediately indicating that the disproportionation reaction was taking place rapidly. Free chlorine dioxide is the molecular chlorine dioxide in the form of a water soluble yellow gas. Total available chlorine dioxide is the amount of free chlorine dioxide which could be generated from a given chlorite solution if it was all converted to C102.
Numerous other experiments were conducted under the same conditions, with essentially the same results, as shown in Table I.
For example, a solution made up by dissolving 3 grams of 80%
technical sodium chlorite and 15 grams of sodium chloride in 3 liters of water was passed through the Pepcon cell at 106 cc/min. The cell drew a current of 3.2-3.3 amps at 6 volts DC.
The total available chlorine dioxide before electrolysis was 564 ppm at a pH of 7.2. After electrolysis, the pH of the solution was 11.1, the free chlorine dioxide was 310 ppm and the total available chlorine dioxide was 430 ppm. This gave a conversion of 55% based on the original total available chlorine dioxide and 72% based on the total available chlorine dioxide available in the effluent from the cell. In 30 minutes the color had almost disappeared from the solution (20 ppm free) and the pH
had decreased to 8.48, indicating that the disproportionation reaction had occured.
Since the disproportionation reaction does not occur to any extent at lower pH, the cell was then operated with a solution designed to maintain the pH below 7-8. This approach is wherein the invention lies. Several systems should be considered for control of the effluent pH, namely potassium acid phthalate, boric acid, sodium bicarbonate, and sodium dihydrogen phosphate plus any other system capable of pH control. Examples of the use of each of these systems are given in Table I, Runs 14-18.
The pH of the effluents from these runs are in the range of 5-9.
No loss of chlorine dioxide was noted over time due to the disproportionation reaction. In addition, periodic removal of sodium hydroxide from the cathode was not required (as with the membrane cell) since the sodium hydroxide and hydrogen produced is in the pipe cell's effluent. In small cells the hydrogen production is not a problem but in larger cells it should be vented from the cell electrolyte.
Of course, a similar result can be obtained by omitting the buffers used in Runs 14-18 and then adjusting the pH of the effluent by adding acid but this adds an extra step to the process and requires complicated equipment to add acid to a controlled pH. Additionally, the disproportation reaction takes place until the pH is lowered, resulting in some loss of chlorine dioxide.
The electrolysis of a 2% stabilized chlorine dioxide is carried out by adding an appreciable quantity of a reagent (2 to 20 grams per liter, preferably 10 gpl) which is capable of forming a buffer with the ingredients of Carnebon 200TM, such boric acid, sodium dihydrogen phosphate, potassium acid phthalate, or sodium bicarbonate, etc. This solution is then passed through a Pepcon 20 amp. laboratory cell at the optimum rate of flow to give maximum conversion to free chlorine dioxide. The conversion is at least 60% and the pH of the resulting solution is below 10, preferably in the range of 8 - 9.
This pH range prevents the disproportionation of chlorine dioxide to chlorate and chlorite. The Pepcon cell has a lead oxide stabilized graphite anode and a stainless steel cathode.
The applied voltage can vary between 3 -12 volts D.C. The pipe cell is identical to the Pepcon cell except that the anode is a dimensionally stable anode as described above.
A less desirable alternative is to add acid or buffers to the effluent to reduce the pH from 11 - 12 down to 8 - 9, rather than including them in the cell feed. This approach will prevent the disproportionation reaction from proceeding, but there is some loss due to the speed of the reaction before the buffering takes effect.
Another alternative is to pass the effluent through an acid ion exchange resin to lower the pH of the solution to 8 - 9 to prevent the undesirable disproportination reaction from taking place. Another possible approach to pH control is dilution with neutral or acidic water.
EXAMPLES
Example 1.
A solution of Anthium Dioxcide , containing 50,000 ppm stabilized chlorine dioxide was run through the flow cell shown in Figure I
at a flow rate of about 50 cc/minute. The voltage was 6 volts and the current was 5 amperes. The Anthium Dioxcide contains a sodium carbonate - sodium bicarbonate buffer. The conversion was high, as evidenced by the dark orange color of the effluent.
The run was terminated immediately due to the high concentration of chlorine dioxide being generated and no quantitative data was determined for this run.
Example 2.
Carnebon 200 , which contains 20,000 ppm stabilized chlorine dioxide is run through the flow cell at a rate of 30 cc/minute, 6 volts and 4.8 amperes. The Carnebon 200 contains a sodium carbonate - bicarbonate buffer. It is further buffered by addition of 10 grams/liter of boric acid before the electrolysis. The effluent from the cell is diluted 3/1 with deionized water. The diluted stream should then contain about 3000 ppm free C1O2 and a have pH of 8.3. The solution is stable at this pH with no tendency to disproportionate.
Example 3.
The electrolysis is repeated under the conditions shown in Example 2 except that the boric acid buffer is omitted. The amperes observed in this example will be slightly reduced and on dilution the solution will have, only about 2500 ppm free 0102 and the pH should be about 8.9. The solution will not lose its yellow color, which would indicate disproporination and a decreased chlorine dioxide concentration.
Example 4.
Carnebon 200 is diluted 1/1 with deionized water to give a feed solution containing 10,000 ppm total available chlorine dioxide.
This solution is then passed through the flow cell of Figure 1 at a rate of 25 cc/minute, at 6 volts and 4.3 amperes. After electrolysis, the solution should be immediately diluted 1/1 with deionized water and should contain a Cl02 concentration of about 3000 ppm free C1O2 and have pH of 8.9. No decolorization of the solution should be observed on standing.
Example 5.
A solution of 1 gram per liter of sodium chlorite, 5 grams per liter of sodium chloride, and 2 grams per liter of potassium hydrogen phthalate (KHP) was prepared. This solution was passed through the electrolysis cell at a rate of 125 cc/min. at 6 volts, giving a current of 2.9 amps. The resulting undiluted solution had a free chlorine dioxide concentration of 350 ppm and a total available chlorine dioxide concentration giving an 85% conversion. The solution had a pH of 5.6, was stable and did not disproportionate to chlorite and chlorate.
Example 6.
The solution of Example 5. was passed through the same cell at a rate of 150 cc/min. and a current of 3 amperes. The resulting solution had a free chlorine dioxide content of 330 ppm and a total available chlorine dioxide content of 421 ppm for a conversion of 78%.
Example 7.
A solution of 1 gram per liter of sodium chlorite, 5 grams per liter of sodium chloride, and 2 grams per liter of boric acid was prepared. This solution was passed through the cell at a rate of 100 cc/min. at 6 volts and 2.6 amperes current. The effluent had a free chlorine dioxide content of 350 ppm and a total available chlorine dioxide content of 389 ppm for a conversion of 90%. The pH of the solution was 8.3. This solution showed no tendency to disproportionate.
Example 8.
A solution of 1 gram per liter of sodium chlorite, 5 grams per liter of sodium chloride, and 2 grams per liter of sodium bicarbonate was passed through the cell at a rate of 100 cc/min.
at 6 volts and 3 amperes current. The effluent from the cell had a pH of 8.9, a free chlorine dioxide content of 150 ppm and a total available chlorine dioxide content of 364 ppm for a conversion of 41%. The solution was stable in color.
Example 9.
A solution containing 1 gram per liter of sodium chlorite and 5 grams per liter of sodium chloride was electrolyzed at a feed rate of 106 cc/min. at 6 volts and 3.2 amperes. The effluent from the cell had a pH of 11.1, a free chlorine dioxide content of 310 ppm and a total available chlorine dioxide content of 430 ppm for a conversion of 72%. The high pH effluent began to immediately disproportionate to chlorite and chlorate. Very quickly this solution became colorless indicating complete loss of the free chlorine dioxide in solution.
Example 10.
Example 2 is repeated except that 10 grams per liter of sodium chloride is added to the Carnebon 200 stabilized chlorine dioxide solution before electrolysis. The electrolysis conditions are repeated exactly as in Example 2. After dilution with 3 parts water to 1 part of the cell effluent electrolyte should have 4000 ppm free chlorine dioxide and a pH of 8.3, with no tendency to disproportionate.
Example 11.
Example 9 is repeated using an eductor downstream from the cell.
Municipal water is supplied to the eductor and the effluent from the cell is fed into the throat of the eductor. The flow rates of the effluent stream and the municipal water stream are adjusted so that the final concentration of the free chlorine dioxide is 5 ppm. The pH of the total stream should be about 9.5 and the color of the solution should be stable. No appreciable disproportination should occur.
Example 12.
Example 11 is repeated but an acid or an acidic buffer is added to the throat of the eductor in an amount sufficient to give a pH in the range of 7 to 8.9. The color of the solution should be stable and should contain 5 ppm free chlorine dioxide and should show no decrease.
Example 13.
A solution containing 31,400 ppm of sodium chlorate is mixed 1:1 by volume with 20,000 ppm of stabilized chlorine dioxide, to provide a solution containing 15,704 ppm of sodium chlorate and 13,422 ppm of sodium chlorite. Two grams per liter of potassium acid phthalate is added to this solution. It is passed through a Pepcon cell at a rate of 150 cc/minute at a voltage of 6 volts and a current of about 4.5 amperes. When 1 part of the effluent from the cell is diluted with 4 parts water, the concentration of free (molecular) chlorine dioxide should be about 3000 ppm.
This indicates some reduction of the chlorate to chlorine dioxide as well as the oxidation of chlorite to chlorine dioxide in the same electrolytic cell.
Example 14.
A total of 60 parts of salt water obtained from the ocean (about 30,000 ppm sodium chloride) is mixed with 40 parts of 2%
stabilized chlorine dioxide to give a feed solution containing about 8,000 ppm total available chlorine dioxide and 18,000 ppm sodium chloride as a feed solution for a 5-5M Cloropac0 unit (Electrolytic Hypochlorite Generation Cell). This cell is designed, when operated at a feed rate of 20 gallons per minute to produce 0.5 lbs. per hour of sodium hypochlorite at a concentration of 50 ppm. The effluent from this cell should have a pH of about 8.9 and a free chlorine dioxide content of 500 ppm and 50ppm of sodium hypochlorite. After dilution, this solution can be used as an antimicrobial in the water used for cooling, ballast water, effluent sewage treatment and the main on-board seawater flow. The effluent from this cell can also be used in the condenser cooling in power plants and offshore oil drilling and production facilities to control marine growth.
Slower feed rates will tend to give higher conversions to chlorine dioxide and sodium hypochlorite. When seawater feed is used, it should be noted that additional buffer should be added to control the pH of the effluent in the presence of the generated sodium hypochlorite. If fresh water, containing no salt, is used to dilute the stabilized chlorine dioxide or neat stabilized chlorine dioxide alone is used as feed without the chloride, no additional buffer may be required and chlorine dioxide alone will result, with no co-produced sodium hypochlorite.
Example 15. A solution containing 5 grams/liter of sodium chlorite, 7.5 grams per liter of sodium chloride, and 10 grams per liter of sodium dihydrogen phosphate was passed through the pipe cell having a dimensionally stable center anode at a rate of 30 gallons per day at 12 volts and 20 amps. The temperature of the cell electrolyte was 12 degrees Centigrade and the pH was 6.2. The molecular chlorine dioxide content of the solution was 1252 ppm from a total available C1O2 content of 2197 ppm, giving a conversion of 57% (Run #5 in Table I). At this pH there was no tendency towards disproportionation of the chlorine dioxide to chlorate and chlorite.
Example 16. A solution containing 5.0 grams per liter of stabilized chlorine dioxide and 10 grams per liter of NaH2PO4 was electrolyzed through the same cell as in Example 15 at a rate of 17.5 ml per minute, giving a residence time of 13.1 minutes for the solution in the cell. The voltage was 12 and the current was 9 amps, giving a cell effluent having a pH of 5.9 and 720 ppm of free (molecular) 0102 from a solution having a total available C1O2 content for a 60.9% conversion. Again there was no loss of chlorine dioxide through disproportionation.
Example 17. A solution containing 6.0 grams per liter of sodium chloride, 1.0 gram per liter of sodium bromide and 2.0 grams of potassium hydrogen phthalate is passed through the pipe cell at a rate of 200 ml. per minute. The voltage in the cell was 12 volts and the current was 7.0 amps. The amount of HOBr produced in the solution was 1336 ppm at a pH of 5.7.
Claims (15)
1. An electrolytic process for generating a stable solution of chlorine dioxide, which process comprises the steps of:
a) preparing an aqueous solution containing chlorite ions in a concentration of about 10 to about 80,000 ppm;
b) adding a buffering agent or an acid to the aqueous chlorite solution in an amount sufficient to control the pH
of the chlorine dioxide solution at a pH of about 9.5 or below after electrolysis;
c) up flowing the buffered or acidified aqueous chlorite solution through an electrolytic cell containing an anode and a cathode, but no membrane, at a voltage of about 1 volt to about 12 volts to electrolyze the chlorite to chlorine dioxide and generate the stable solution of chlorine dioxide; and d) removing the stable solution of chlorine dioxide as the effluent from the top of the electrolytic cell.
a) preparing an aqueous solution containing chlorite ions in a concentration of about 10 to about 80,000 ppm;
b) adding a buffering agent or an acid to the aqueous chlorite solution in an amount sufficient to control the pH
of the chlorine dioxide solution at a pH of about 9.5 or below after electrolysis;
c) up flowing the buffered or acidified aqueous chlorite solution through an electrolytic cell containing an anode and a cathode, but no membrane, at a voltage of about 1 volt to about 12 volts to electrolyze the chlorite to chlorine dioxide and generate the stable solution of chlorine dioxide; and d) removing the stable solution of chlorine dioxide as the effluent from the top of the electrolytic cell.
2. An electrolytic process for generating a stable solution of chlorine dioxide, which process comprises the steps of:
a) preparing an aqueous solution containing a chlorite and a chlorate, and a buffering agent or an acid capable of maintaining the pH at below about 7.0 after electrolysis;
b) up flowing the buffered or acidified aqueous solution through an electrolytic cell which comprises an anode and a cathode, but no membrane, at a voltage of about 1 volt to about 12 volts to electrolyze the chlorite solution and generate the stable solution of chlorine dioxide; and c) removing the stable solution of chlorine dioxide as the effluent from the top of the electrolytic cell.
a) preparing an aqueous solution containing a chlorite and a chlorate, and a buffering agent or an acid capable of maintaining the pH at below about 7.0 after electrolysis;
b) up flowing the buffered or acidified aqueous solution through an electrolytic cell which comprises an anode and a cathode, but no membrane, at a voltage of about 1 volt to about 12 volts to electrolyze the chlorite solution and generate the stable solution of chlorine dioxide; and c) removing the stable solution of chlorine dioxide as the effluent from the top of the electrolytic cell.
3. An electrolytic process for generating a stable solution of chlorine dioxide, which process comprises the steps of:
a) preparing an aqueous solution of stabilized chlorine dioxide, which contains about 10 to about 80,000 ppm of chlorite ions as the sodium salt and contains a buffering agent in an amount sufficient to adjust the pH of the solution before electrolysis to about 8.5 to about 9.5.
b) up flowing the buffered aqueous solution through an electrolytic cell containing an anode and a cathode, but no membrane, at a voltage of about 1 volt to about 12 volts to electrolyze the sodium chlorite and generate the stable solution of chlorine dioxide; and c) removing the stable solution of chlorine dioxide as the effluent from the top of the electrolytic cell.
a) preparing an aqueous solution of stabilized chlorine dioxide, which contains about 10 to about 80,000 ppm of chlorite ions as the sodium salt and contains a buffering agent in an amount sufficient to adjust the pH of the solution before electrolysis to about 8.5 to about 9.5.
b) up flowing the buffered aqueous solution through an electrolytic cell containing an anode and a cathode, but no membrane, at a voltage of about 1 volt to about 12 volts to electrolyze the sodium chlorite and generate the stable solution of chlorine dioxide; and c) removing the stable solution of chlorine dioxide as the effluent from the top of the electrolytic cell.
4. An electrolytic process for generating a stable solution of chlorine dioxide, which process comprises the steps of:
a) preparing an aqueous solution of sodium chlorite ions in a concentration of about 10 to about 80,000 ppm as sodium chlorite;
b) up flowing the aqueous chlorite solution through an electrolytic cell containing an anode and a cathode, but no membrane, at a voltage of about one volt to about 12 volts to electrolyze the sodium chlorite and generate the stable solution of chlorine dioxide; and c) removing the solution of chlorine dioxide as the effluent from the top of the electrolytic cell; and d) immediately mixing the chlorine dioxide-containing effluent with a solid buffering agent or with a solution containing a buffering agent, which buffering agent is capable of maintaining the chlorine dioxide solution at a pH
below about 9.5 to form the stable solution of chlorine dioxide.
a) preparing an aqueous solution of sodium chlorite ions in a concentration of about 10 to about 80,000 ppm as sodium chlorite;
b) up flowing the aqueous chlorite solution through an electrolytic cell containing an anode and a cathode, but no membrane, at a voltage of about one volt to about 12 volts to electrolyze the sodium chlorite and generate the stable solution of chlorine dioxide; and c) removing the solution of chlorine dioxide as the effluent from the top of the electrolytic cell; and d) immediately mixing the chlorine dioxide-containing effluent with a solid buffering agent or with a solution containing a buffering agent, which buffering agent is capable of maintaining the chlorine dioxide solution at a pH
below about 9.5 to form the stable solution of chlorine dioxide.
5. The process of Claim 1, 2, 3, or 4, further comprising the step of diluting the stable solution of chlorine dioxide to a concentration which is effective for disinfecting, sanitizing, or deodorizing.
6. The process of Claim 1 or 2, wherein the chlorite ions are from an alkali metal chlorite or alkaline earth metal chlorite.
7. The process of Claim 6, wherein the alkali metal chlorite is sodium chlorite.
8. The process of Claim 6, wherein the alkaline earth metal chlorite is calcium chlorite.
9. The process of Claim 1, 2, 3, or 4, wherein the buffering agent is an alkali metal citrate, acetate, phosphate, borate, or carbonate.
10. The process of Claim 1, 2, 3, or 4, wherein the electrolytic cell contains a dimensionally stable metal anode.
11. The process of Claim 10, wherein the metal anode is titanium coated with a precious metal.
12. The process of Claim 11, wherein the precious metal is platinum, palladium, or iridium.
13. The process of Claim 1, 2, 3, or 4, wherein the electrolytic cell is designed for the production of chlorine from sea water or solutions containing sodium chloride.
14. The process of Claim 13, wherein the electrolytic cell is designed for the production of sodium hypochlorite from sea water.
15. The process of Claim 1, 2, or 3, further comprising the step of adjusting the pH of the effluent by adding at least one of an acid or a buffering agent, or by passing the effluent through an acid ion exchange resin, or by diluting the effluent with neutral or acidic water.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2000/032406 WO2003025252A1 (en) | 2001-01-16 | 2001-01-16 | An electrolytic process for the generation of stable solutions of chlorine dioxide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2429908A1 CA2429908A1 (en) | 2003-03-27 |
| CA2429908C true CA2429908C (en) | 2011-05-17 |
Family
ID=21742032
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2429908A Expired - Fee Related CA2429908C (en) | 2001-01-16 | 2001-01-16 | An electrolytic process for the generation of stable solutions of chlorine dioxide |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP1370715A1 (en) |
| CA (1) | CA2429908C (en) |
| WO (1) | WO2003025252A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100377991C (en) * | 2003-05-19 | 2008-04-02 | 宝洁公司 | Compositions, devices and methods for stabilizing and increasing the efficacy of halogen dioxide solutions |
| KR100542895B1 (en) * | 2003-12-22 | 2006-01-11 | 재단법인 포항산업과학연구원 | Method for controlling ballast water using effect of NaOCl produced electrolysis of natural seawater and an apparatus for the same |
| EP1979269A4 (en) | 2005-12-22 | 2013-01-02 | Taiji Biomedical Inc | Chlorite formulations, and methods of preparation and use thereof |
| CN101623238B (en) * | 2008-07-11 | 2013-02-13 | 黄冰燃 | Long-acting deodorization composition for animals and preparation method thereof |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5429723A (en) * | 1987-10-27 | 1995-07-04 | Cogent Limited | Hypobromination of water |
| US5320806A (en) * | 1990-01-05 | 1994-06-14 | Allegan, Inc. | Methods to disinfect contact lenses |
| US6306281B1 (en) * | 1999-11-30 | 2001-10-23 | Joseph Matthew Kelley | Electrolytic process for the generation of stable solutions of chlorine dioxide |
-
2001
- 2001-01-16 CA CA2429908A patent/CA2429908C/en not_active Expired - Fee Related
- 2001-01-16 EP EP00993769A patent/EP1370715A1/en not_active Ceased
- 2001-01-16 WO PCT/US2000/032406 patent/WO2003025252A1/en active Application Filing
Also Published As
| Publication number | Publication date |
|---|---|
| WO2003025252A1 (en) | 2003-03-27 |
| EP1370715A1 (en) | 2003-12-17 |
| CA2429908A1 (en) | 2003-03-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6306281B1 (en) | Electrolytic process for the generation of stable solutions of chlorine dioxide | |
| US5965004A (en) | Chlorine dioxide generation for water treatment | |
| US5174868A (en) | Chlorine dioxide generation from chloric acid | |
| US4456510A (en) | Process for manufacturing chlorine dioxide | |
| US4542008A (en) | Electrochemical chlorine dioxide process | |
| US4405465A (en) | Process for the removal of chlorate and hypochlorite from spent alkali metal chloride brines | |
| EP0612685B1 (en) | Process for producing chlorine dioxide | |
| EP0698000B1 (en) | Chlorine dioxide generation for water treatment | |
| US10046990B2 (en) | Electrolytic method of generating chloride dioxide with improved theoretical yield | |
| US5122240A (en) | Electrochemical processing of aqueous solutions | |
| US5935393A (en) | Apparatus for producing hypochlorite | |
| CA1214429A (en) | Removal of chlorate from electrolyte cell brine | |
| FI90790B (en) | Combined process for the production of chlorine dioxide and sodium hydroxide | |
| US6740223B2 (en) | Electrolytic process for the production of chlorine dioxide | |
| US5419818A (en) | Process for the production of alkali metal chlorate | |
| RU2104247C1 (en) | Method of preparing chlorine dioxide (variants) | |
| US8216443B2 (en) | Process for producing alkali metal chlorate | |
| US20020130048A1 (en) | Process for the production of hydrogen peroxide solution | |
| CA2429908C (en) | An electrolytic process for the generation of stable solutions of chlorine dioxide | |
| US5851374A (en) | Process for production of chlorine dioxide | |
| KR20150036485A (en) | Electrochemical generation of chlorinated urea derivatives | |
| EP0532535B2 (en) | Electrochemical production of acid chlorate solutions | |
| JPH0938655A (en) | Electrolytic hypochlorous bactericide water containing ozone, its production and device therefor | |
| US5284553A (en) | Chlorine dioxide generation from chloric acid | |
| JPH05179475A (en) | Production of hypochlorite |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |
Effective date: 20170116 |