The invention relates to the production of chlorine dioxide (ClO2) and particularly to a suitable electrode element and a catalytic process for the production of chlorine dioxide.
Historically, ClO2 has been commercially prepared by a reaction between a metal chlorate in aqueous solution, such as sodium chlorate (NaClO3), and a relatively strong acid such as sulphuric, phosphoric or hydrochloric acid.
Generally, processes for generating ClO2 make use an alkali chlorate-containing feedstock, usually NaClO3, that also includes a halide salt of alkali metal or other reducing agents. The sodium chlorate feedstock for such a ClO2 production process is typically generated by electrolysis of sodium chloride brine in any well-known manner. When chlorides are used as the reducing agent, the mixture of brine and chlorate is directly fed to one or more reactors where the feedstock contacts a desired acid and reacts to form ClO2. Due to the high amount of acidity required, e.g. 5-10N acid, coupled with the need for a reducing agent, small scale production of ClO2 from NaClO3 is not practiced. Examples of ClO2 generation processes via electrochemical or catalytic reduction of sodium chlorate in strong acid are reported for example in U.S. Pat. Nos. 4,501,824, 426,263, 4,381,290 and 4,362,707. These prior art teachings allow to dispense with the need for a separate reducing agent, still requiring however a chemical supply of acid in the process.
Under one aspect, the invention relates to an electrode element comprising a valve metal substrate; a first catalyst component applied to said substrate, said first catalyst component suitable for evolving oxygen from an aqueous solution under anodic polarisation; a second catalyst component suitable for generating chlorine dioxide from a chlorate solution in acidic environment; said first and second catalyst component being electrically insulated from each other.
By virtue of the above arrangement, the anodic evolution of oxygen with the consequent generation of protons brings about a lowering of the local pH of the solution at the surface of the second catalyst component. In other words, the electrochemical anodic reaction produces the acid concentration suitable for carrying out the catalytic reduction of chlorate to chlorine dioxide without the need of any external addition of acid. The electrode element of the invention is then suitable for generating chlorine dioxide starting from water and a chlorate solution only, thus avoiding the handling of strong mineral acids such as sulphuric acid.
With electrode element it is herewith intended an integral electrode comprising two distinct catalyst components arranged in a single stand-alone piece, the two catalyst components being either spaced apart by means of a suitable insulating spacer, or in intimate contact but electrically insulated from each other.
In one embodiment, the second catalyst component of the electrode element is supported on a ceramic support. The ceramic support, for example, can be in the form a discrete ceramic media such as distillation saddles.
In another embodiment, the second catalyst component of the electrode element is supported on a metallic support.
This second catalyst component can be optionally polarized to a lower potential to enhance the production of chlorine dioxide.
In one embodiment, the second catalyst component of the electrode element is connected to a power supply.
In one embodiment, the first catalyst component of the electrode element comprises noble metal oxides.
In one embodiment, in the electrode element according to the invention the second catalyst component is a mixture of noble metal oxides selected from the group consisting of ruthenium oxide, iridium oxide, palladium oxide, rhodium oxide and platinum oxide. Optionally, the second catalyst component also comprises a valve metal oxide.
In one embodiment, the second catalyst component of the electrode element is in the form of a ceramic or metallic sheet or mesh or of a porous material.
Under another aspect, the invention relates to an electrolytic cell comprising at least one electrode element as described above.
In one embodiment, the electrolytic cell is equipped with electrode elements disposed as an array of intercalated first catalyst components applied to substrates and second catalyst components, the first and second catalyst components being reciprocally insulated.
Under yet another aspect, the invention relates to a process for the generation of chlorine dioxide on a catalyst component comprising the steps of:
Preferably, the solution is electrolyzed at a temperature of 40° C. to 90° C.
The following examples are included to demonstrate particular embodiments of the invention, whose practicability has been largely verified in the claimed range of values. It should be appreciated by those of skill in the art that the compositions and techniques disclosed in the examples which follow represent compositions and techniques discovered by the inventors to function well in the practice of the invention; however, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the scope of the invention.
An electrochemical cell comprising a 0.5 cm-diameter coated titanium rod as the anode was prepared. The coating of the anode consisted of 10 g/m2 of mixed oxides of iridium and tantalum in a 2:1 molar ratio. A coated titanium expanded mesh serving as support for the second catalyst element was wrapped around the rod with a spacer arranged therebetween to provide for electrical insulation. The coating of the titanium mesh consisted of 10 g/m2 of RuO2/RhO2 in a 1:2 molar ratio. A 2M NaClO3 solution was supplied as the electrolyte feedstock. The reaction was carried out at a temperature of 61° C. and at an anode current density of 50 mA/cm2.
The test was run for 5 hours. A sample was taken every one hour and characterised in a UV/VIS Spectrophotometer (Hach DR 5000). The FIGURE shows the increase in chlorine dioxide concentration as a function of time.
The previous description shall not be intended as limiting the invention, which may be used according to different embodiments without departing from the scopes thereof, and whose extent is solely defined by the appended claims.
Throughout the description and claims of the present application, the term “comprise” and variations thereof such as “comprising” and “comprises” are not intended to exclude the presence of other elements, components or additional process steps.
The discussion of documents, acts, materials, devices, articles and the like is included in this specification solely for the purpose of providing a context for the present invention. It is not suggested or represented that any or all of these matters formed part of the prior art base or were common general knowledge in the field relevant to the present invention before the priority date of each claim of this application.
This application is a U.S. national stage of PCT/EP2015/066378 filed on Jul. 17, 2015 which claims the benefit of priority from U.S. Provisional Patent Application No. 62/025,557 filed Jul. 17, 2014 the contents of each of which are incorporated herein by reference.
Filing Document | Filing Date | Country | Kind |
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PCT/EP2015/066378 | 7/17/2015 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
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WO2016/009031 | 1/21/2016 | WO | A |
Number | Name | Date | Kind |
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426263 | Goff | Apr 1890 | A |
3873437 | Pulver | Mar 1975 | A |
4362707 | Hardee et al. | Dec 1982 | A |
4381290 | Hardee et al. | Apr 1983 | A |
4388162 | Sammells et al. | Jun 1983 | A |
4426263 | Hardee | Jan 1984 | A |
4501824 | Hardee et al. | Feb 1985 | A |
6203688 | Lipsztajn et al. | Mar 2001 | B1 |
Number | Date | Country |
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2157827 | Mar 1997 | CA |
Entry |
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B.R. Deshwal & H.K. Lee. “Manufacture of Chlorine Dioxide from Sodium Chlorate: State of the Art” Journal of Industrial and Engineering Chemistry . vol. 11, No. 3. pp. 330-346 (Year: 2005). |
International Search Report and Written Opinion for International Application No. PCT/EP2015/066378 (dated Oct. 19, 2015) (7 Pages). |
International Preliminary Report on Patentability for International Application No. PCT/EP2015/066378 (dated Jul. 22, 2016) (13 Pages). |
Number | Date | Country | |
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20170211194 A1 | Jul 2017 | US |
Number | Date | Country | |
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62025557 | Jul 2014 | US |