EP0197981A1 - Catalytic polymer electrode for cathodic protection and cathodic protection system comprising same. - Google Patents
Catalytic polymer electrode for cathodic protection and cathodic protection system comprising same.Info
- Publication number
- EP0197981A1 EP0197981A1 EP19850904921 EP85904921A EP0197981A1 EP 0197981 A1 EP0197981 A1 EP 0197981A1 EP 19850904921 EP19850904921 EP 19850904921 EP 85904921 A EP85904921 A EP 85904921A EP 0197981 A1 EP0197981 A1 EP 0197981A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- catalytic
- polymer
- valve metal
- electrode
- anode
- 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.)
- Granted
Links
- 230000003197 catalytic effect Effects 0.000 title claims abstract description 100
- 229920000642 polymer Polymers 0.000 title claims abstract description 77
- 238000004210 cathodic protection Methods 0.000 title claims abstract description 29
- 239000002245 particle Substances 0.000 claims abstract description 42
- 239000002923 metal particle Substances 0.000 claims abstract description 23
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 22
- 229920001940 conductive polymer Polymers 0.000 claims abstract description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 20
- 239000002322 conducting polymer Substances 0.000 claims abstract description 20
- 239000003054 catalyst Substances 0.000 claims abstract description 18
- 229910052751 metal Inorganic materials 0.000 claims abstract description 15
- 239000002184 metal Substances 0.000 claims abstract description 15
- 238000004519 manufacturing process Methods 0.000 claims abstract description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 4
- 239000001301 oxygen Substances 0.000 claims abstract description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 17
- 239000010936 titanium Substances 0.000 claims description 15
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 14
- 229910052719 titanium Inorganic materials 0.000 claims description 14
- 239000010970 precious metal Substances 0.000 claims description 13
- 229910052707 ruthenium Inorganic materials 0.000 claims description 11
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 10
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 239000000835 fiber Substances 0.000 claims description 8
- 238000003825 pressing Methods 0.000 claims description 7
- 229910052715 tantalum Inorganic materials 0.000 claims description 7
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 7
- 239000004416 thermosoftening plastic Substances 0.000 claims description 7
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 6
- 229920000098 polyolefin Polymers 0.000 claims description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 5
- 239000010411 electrocatalyst Substances 0.000 claims description 5
- 229910052741 iridium Inorganic materials 0.000 claims description 5
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 5
- 239000010955 niobium Substances 0.000 claims description 5
- 229910052758 niobium Inorganic materials 0.000 claims description 5
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 5
- 229910052763 palladium Inorganic materials 0.000 claims description 5
- 229910052697 platinum Inorganic materials 0.000 claims description 5
- 229910052703 rhodium Inorganic materials 0.000 claims description 5
- 239000010948 rhodium Substances 0.000 claims description 5
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 5
- 229910052726 zirconium Inorganic materials 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 claims description 4
- 238000007254 oxidation reaction Methods 0.000 claims description 4
- 229920000178 Acrylic resin Polymers 0.000 claims description 2
- 239000004925 Acrylic resin Substances 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- 238000001816 cooling Methods 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 150000008282 halocarbons Chemical class 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 239000000758 substrate Substances 0.000 claims 2
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 239000004020 conductor Substances 0.000 claims 1
- 229910044991 metal oxide Inorganic materials 0.000 claims 1
- 150000004706 metal oxides Chemical class 0.000 claims 1
- 229910001925 ruthenium oxide Inorganic materials 0.000 claims 1
- WOCIAKWEIIZHES-UHFFFAOYSA-N ruthenium(iv) oxide Chemical compound O=[Ru]=O WOCIAKWEIIZHES-UHFFFAOYSA-N 0.000 claims 1
- 229910000831 Steel Inorganic materials 0.000 abstract description 9
- 239000010959 steel Substances 0.000 abstract description 9
- 239000011150 reinforced concrete Substances 0.000 abstract description 5
- 239000007789 gas Substances 0.000 abstract description 3
- 239000000446 fuel Substances 0.000 abstract description 2
- 238000003860 storage Methods 0.000 abstract description 2
- 239000004567 concrete Substances 0.000 description 8
- 230000007797 corrosion Effects 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- 229920000049 Carbon (fiber) Polymers 0.000 description 5
- 230000003213 activating effect Effects 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000004917 carbon fiber Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 229910001294 Reinforcing steel Inorganic materials 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000002787 reinforcement Effects 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000005553 drilling Methods 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000914 Metallic fiber Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229910019891 RuCl3 Inorganic materials 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 239000011231 conductive filler Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229910021397 glassy carbon Inorganic materials 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000011440 grout Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000412 polyarylene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- YBCAZPLXEGKKFM-UHFFFAOYSA-K ruthenium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Ru+3] YBCAZPLXEGKKFM-UHFFFAOYSA-K 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F13/00—Inhibiting corrosion of metals by anodic or cathodic protection
- C23F13/02—Inhibiting corrosion of metals by anodic or cathodic protection cathodic; Selection of conditions, parameters or procedures for cathodic protection, e.g. of electrical conditions
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F2201/00—Type of materials to be protected by cathodic protection
- C23F2201/02—Concrete, e.g. reinforced
Definitions
- the present invention relates to catalytic polymer electrodes which comprise an electrocatalyst applied to a current conducting polymer body forming an electrode base.
- catalytic polymer electrodes which comprise an electrocatalyst applied to a current conducting polymer body forming an electrode base.
- Use of the catalytic polymer electrode in an impressed-current cathodic protection system and a method of making the catalytic polymer electrode are also disclosed.
- cathodic protection is effective to prevent corrosion of reinforcing steel in concrete bridge decks, support structures, and parking garages, which are subject to extensive damage by corrosion of the steel reinforcement due to the presence of salt and moisture in the normally alkaline concrete environment.
- Such damage of reinforced concrete by corrosion results more particularly from the practice of spreading large amounts of salt on roads in winter, while coastal structures are attacked by seawater and salt spray.
- a known type of polymer anode commercially availiable for use in impressed-current cathodic protection systems consists of a carbon loaded, current conducting polymer body with a copper core and operates at a current density limited to a maximum of about 0.02 A/m 2 to avoid causing damage to the polymer anode surface.
- Another type of anode which is used for cathodic protection of reinforcing steel consists of carbon fibers which are placed in a groove in the concrete, the groove then being filled with a grout of electronically conductive carbon-loaded backfill.
- the use of carbon presents serious limitations, since this material is subject to high operating voltages and therefore a limited lifetime as an anode. This is a serious limitation since replacement of anodes embedded in concrete is very difficult.
- This type of anode also has a high electronic resistivity, so that current can be carried longitudinally only over very short distances through the carbon fibers.
- anodes which are traditionally used for impressed current cathodic protection are constructed of platinized titanium or platinized tantalum with a more electronically conductive copper core. Such electrodes are often used for cathodic protection of underground pipelines, well casings, ship hulls, jetties, drilling rigs, and oil platforms. These electrodes are expensive and must therfore be used at a higher current density, up 2 to 1000 A/m in some cases. The expense of such platinized titanium or tantalum electrodes entails special design problems since a very low current density must be applied to the structure being cathodically protected. This results in a mismatch of current density between anode and cathode. Various system designs attempt to accomodate this mismatch, usually by installation of small anodes at certain locations which are intended to protect large structures over great distances. Unfortunately, this often leads to unforeseen current density disparities and inadequate protection of more distant parts of the structure.
- An object of the invention is to provide long life catalytic polymer electrodes which comprise an electrocatalyst applied to the surface of a current conducting polymer body forming an electrode base.
- Another object of the invention is to provide a catalytic polymeric anode which presents substantially the same advantages as known carbon loaded, current conducting polymeric anodes for cathodic protection systems, but which can operate at a significantly reduced potential with an extended service life at a higher current density.
- a further object of the invention is to provide such a catalytic polymeric anode with a long service life which is more particularly suitable for the cathodic protection of reinforced concrete structures, such as bridge decks, parking garages, and coastal structures exposed to seawater and salt spray.
- Another object of the invention is to provide such a catalytic polymeric anode which is more particularly suitable for the cathodic protection of underground pipelines, well casings, ship hulls, jetties, drilling rigs, oil platforms, and the like.
- a catalytic polymer electrode is provided with catalytic valve metal particles which are fixed to the surface of a current conducting polymer body forming an electrode base.
- the catalytic polymer electrode according to the invention may comprise an electrode base formed of any suitable current conducting polymer body.
- a carbon loaded polymer may advantageously form a current conducting polymer body to provide such an electrode base.
- the catalytic polymer electrode according to the invention will preferably comprise an electrode base consisting of a current conducting body made from thermoplastic polymer compounds.
- the preferred thermoplastic resins include: polyolefins such as polymers of ethylene and/or propylene; halocarbon polymers such as polyvinyl chloride, polyvinylidene fluoride and halogen substituted olefinic polymers; styrenic polymers such as polystyrene, and copolymers of styrene with acryonitrile, etc; polyamides such as polycaprolactam; the thermoplastic polyesters; and the acrylic resins such as polyacrylates and polymethacrylates.
- thermoplastics including polyimides; polyarylene resins, such as polycarbonates, polysulfones and polyphenylene oxides and sulfides; and various heterocyclic resins may also be used.
- the invention provides a particularly simple method of manufacturing such a catalytic polymer electrode with an extended service life.
- the polymer electrode is made by heating a current conducting body of thermoplastic polymer so as to produce an electrode base with a softened external layer of the thermoplastic polymer and pressing catalytic valve metal particles onto said softened external layer of the polymer.
- the catalytic valve metal particles may advantageously be heated before pressing. The pressing being carried out so that upon cooling a uniform outer layer of said catalytic valve metal particles anchored to the surface of the electrode base is obtained.
- the carbon loaded polymer forming the electrode body is admixed with up to 50% by weight of conductive fibers such as carbon or metallic fibers the polymer electrode obtained upon extrusion of such material around a metallic core, heating of the current conducting body and pressing the catalytic valve metal particles has advantageous properties.
- Such electrodes are found to sustain high electrical currents while avoiding an excessive voltage drop within the electrode.
- the amount of fibers may be as high as 50 weight %, the best results are obtained when the amount of fibers in the carbon loaded polymer is kept in the range of 5 to 30% by weight of the polymer. This is based on finding that the polymer body made with more than 50% of fibers loses its mechanical properties and when the amount of fibers is kept below 5% the conductivity of the polymer body is not adequate.
- Various conductive fibers may be employed eg. carbon, glassy carbon, nickel, copper, aluminium or stainless steel fibers.
- an electrode base of thermoplastic polymer is particularly advantageous in that it allows a catalytic polymer electrode to be produced according to the invention by this extremely simple and reproducible method, while ensuring an excellent fixation and electrical connection of said catalytic particles to the surface of the electrode base.
- the catalytic polymer electrode according to the invention may thus be produced in a highly simplified manner in the form of a continuous electrode of any suitable cross-section, for example in the form of a wire, rod, strip, or sheet.
- the electrode base formed of current conducting, carbon loaded polymer will advantageously comprise an internal metallic reinforcing core, preferably a copper core, which is embedded in the carbon loaded polymer body, in order to allow the catalytic polymer electrode to conduct a,sufficiently high electrical current while avoiding an excessive voltage drop within the electrode.
- the catalytic particles used in the invention will advantageously consist of one of the valve metals: titanium, niobium, tantalum, zirconium, or an alloy thereof which exhibits subtantially the same anodic film-forming properties as these valve metals.
- Catalytic particles of titanium sponge which have an irregular size and shape and are readily deformable may be advantageously pressed into a coherent layer adhering to the electrode base formed of a current conducting polymer body.
- catalytic valve metal particles are advantageously activated with an electrocatalyst which provides a reduced oxygen potential and which may comprise at least one precious metal selected from the group consisting of ruthenium, palladium, iridium, platinum, and rhodium in the metallic state or, preferably, as an oxide.
- a catalytic polymer anode according to the invention provided good results with catalytic particles of titanium sponge comprising a ruthenium based catalyst.
- a very small amount of precious metal may thus be applied to the catalytic valve metal particles and the proportion of precious metal applied may advantageously be at most in the order of 1% by weight of said catalytic particles, but a proportion of precious metal considerably below 1% may be advantageously applied in accordance with the invention.
- This proportion of precious metal applied may preferably lie in the range from 0.1% to about 1.0%, but may if necessary amount up to about 5%.
- the catalytic valve metal particles may be advantageously applied according to the invention with a particle loading in the order of 10 to 100 grams per square meter of the electrode base surface to which they are applied, but this loading may amount to up to 500 grams per square meter or more in some cases.
- the catalytic particles employed according to the invention may be prepared in any suitable manner, for example by a process as described in U.S. Patent
- the catalytic particles may be simply applied, fixed, and electrically connected by pressing them onto the surface of a heated thermoplastic polymer body forming the anode base. These particles may thus be applied by means of rollers, or by drawing the polymer body through a die.
- Catalytic polymer electrodes according to the invention are especially suitable as anodes in impressed current cathodic protection systems in which current
- the catalytic polymer anode of the invention is particularly effective in protecting buried or submerged steel strucures such as gas and oil pipelines.
- catalytic anode can operate at a much higher current density and a much lower potential than the conventional polymer anode.
- catalytic valve metal particles such as are applied according to the invention retain their catalytic activity under extremely harsh anodic corrosion conditions during operation at a many times higher anode current density.
- the catalytic anode according to the invention may thus be expected to exhibit a long service life in cathodic protection systems due to the fact that it can operate at a much lower potential and can thereby protect the current conducting polymer body from damage by oxidation during operation at a relatively high anode current density.
- the activated polymer anode of the invention may be in the form of cable, sheet, wire,, perforated plate or any other convenient form.
- the active catalytic material e.g. RuO-
- the preferred form is the cable.
- the invention may further be illustrated by the fo1lowing examples:
- a catalytic polymer anode was made by applying catalytic titanium particles to an anode base consisting of a conventional current conducting polymer anode of carbon loaded polyolefin with a copper core, which is a conventional, wire-shaped polymer anode (diameter 1 cm) commercially available for • impressed-current cathodic protection.
- the polymer anode body was heated to 120°C for 10 minutes and catalytic titanium particles were then pressed with a roller onto the softened anode surface, which provided good adherence of the catalytic particles to the anode surface.
- the catalytic particles thus applied consisted of activated titanium sponge with a particle size in the range from 300 to 840 micrometers.
- sponge particles were activated by impregnation with an activating solution comprising 2.38 g RuCl 3 .aq.(40 wt % Ru) , and 3.36 g tetra-ortho-butyl titanate dissolved in 3.2 ml concentrated HC1 and 80 ml butylalcohol, then drying at 100°C in air for 120 minutes, and heat treating the dried particles in air at 300°C for 30 minutes, at 425°C for 30 minutes, and finally at 500°C for 10 minutes.
- This activating treatment was carried out 2 times and the catalytic particles thus obtained contained 1 % Ru by weight of Ti.
- the catalytic anode thus obtained was tested in a concrete block containing a steel reinforcement bar, and compared with a conventional polymer anode (without catalyst) as described above.
- the catalytic anode and the conventional polymer anode were symmetrically positioned in the same vertical plane and on op'posite sides of a vertical steel reinforcement bar (at 5 cm from the steel bar), and each anode was provided with a reference electrode (Ag/AgCl) for measuring its single electrode potential (S.E.P).
- a block of concrete (9x13x30 cm) containing 3 8.8 kg/m of NaCl was then cast around the anodes and the steel bar so that they were embedded while their top ends projected from the concrete block for connection to a
- the described catalytic anode operated for 30 days at a constant potential of 0.390 V vs. CSE (Copper Sulfate Electrode) .
- CSE Copper Sulfate Electrode
- the conventional polymer anode exhibited a potential which rose from about 1 V to about 2 V vs. CSE in the first 8 days, decreased slightly to 1.8 V after 20 days, then increased slowly once more to 2.0 V after 30 days.
- the catalytic anode thus operated at a constant potential up to about 1.6 V lower than the non-catalytic anode, while it may be noted that the anode current density applied in this test is several times higher than that at which the described conventional polymer anode can be operated with a satisfactory service life.
- the catalytic anode according to the invention may thus be expected to exhibit a long service life in cathodic protection systems, due to the fact that it can operate at a much lower potential, and can thereby protect the current conducting polymer body from damage by oxidation during operation at a relatively high anode current density.
- the catalytic anode according to the invention may be expected to be functional up to about 500 A/m 2 .
- a catalytic polymer anode 150 meters long was made by applying catalytic particles to an anode base consisting of a carbon loaded polyolefin with a copper core.
- the anode base was first prepared by extruding Union Carbide conductive thermoplastic compound DHDA 7707 around a conductive copper core of #16 A G wire (US standard for wire size) .
- Catalyst was prepared by activating 500 grams of titanium sponge with a particle size in the range of 300 to 840 micrometers. After rinsing in acetone and drying at 120 C, the titanium particles were activated by mixing with an activating solution comprising 17.31 grams
- RuCl- aq. (43 wt.% Ru) in 250ml acetone drying for 2 hours, prebaking at 340°C for 30 minutes, and postbaking 5 at 400°C for 40 minutes. This activating treatment was carried out two times and the catalytic particles thus obtained contained 3% Ru by weight of titanium.
- Catalyst was then continuously applied in a separate step by passing the anode base through a tube furnace at
- a catalytic polymer anode 100 meters long was made by applying catalytic particles to an anode base consisting of carbon loaded polyolefin with a copper core.
- the anode base was first prepared by extruding Union Carbide conductive thermoplastic compound DHOA 7707 around a conductive copper core of #8 AWG wire.
- Catalyst particles were prepared and were applied to the anode base as described in Example II. An anode thus prepared was catalyzed with 300 grams of said particles per square meter of anode surface.
- a catalytic polymer anode was prepared by applying catalytic particles to an anode base consisting of a modified carbon loaded polyolefin with a copper core.
- the anode, base was prepared by extruding a mixture of Union Carbide conductive thermoplastic compound DHDA 7707 with 15% by weight of added carbon fibers around a conductive copper core of #8 AWG wire. Addition of the carbon fibers had the effect of lowering the volumetric resistivity of the polymeric phase from 20 ohm-centimeters to 0.20 ohm-centimeters making possible operation at higher current density.
- Catalytic particles containing 3% Ru by weight of- titanium were prepared as described in Example II, and were then applied to the surface of the anode base by heating the anode base to 120 C for 10 minutes and rolling the catalytic titanium particles onto the softened anode surface.
- the anode thus prepared contained 380 grams of said particles per square meter of anode surface.
- Catalytic polymer electrodes according to the invention are especially suitable as anodes in impressed current cathodic protection systems to prevent corrosion damage of reinforced concrete structures, such as bridge decks, support members, parking garages, or buried or submerged steel strucures such as gas and oil pipelines, offshore production platforms, fuel storage tanks, well casings.
- reinforced concrete structures such as bridge decks, support members, parking garages, or buried or submerged steel strucures
- gas and oil pipelines such as gas and oil pipelines, offshore production platforms, fuel storage tanks, well casings.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Prevention Of Electric Corrosion (AREA)
- Catalysts (AREA)
Abstract
Une électrode polymère catalytique comprend un corps polymère conducteur de courant formant une base d'électrode pourvue de particules de métal "soupape" catalytique fixées sur sa surface. Un corps conducteur de courant en un polymère thermoplastique rempli de carbone est chauffé pour ramollir sa surface externe et les particules de métal "soupape" catalytique sont pressées contre sa surface ramollie et fixées de la sorte sur la surface du corps polymère. Une telle électrode polymère catalytique utilisée en tant qu'anode dans un système de protection cathodique à courant appliqué comprend un catalyseur pour obtenir un potentiel réduit d'oxygène. De telles anodes polymères catalytiques peuvent être appliquées dans des systèmes de protection cathodique à courant appliqué de structures en béton armé, telles que des tabliers supérieurs de ponts, des organes de support, des garages à parkings, ou de structures d'acier enfouies, telles que des pipelines de gaz ou pétrole, des plates-formes de production de haute mer, des citernes de stockage de combustible, des revêtements de puits.A catalytic polymer electrode includes a current conducting polymer body forming an electrode base provided with catalytic "valve" metal particles attached to its surface. A current conducting body of a thermoplastic polymer filled with carbon is heated to soften its external surface and the particles of catalytic "valve" metal are pressed against its softened surface and thus fixed on the surface of the polymer body. Such a catalytic polymer electrode used as an anode in an applied current cathodic protection system comprises a catalyst to obtain a reduced oxygen potential. Such catalytic polymer anodes can be applied in applied current cathodic protection systems of reinforced concrete structures, such as bridge decks, support members, parking garages, or buried steel structures, such as as gas or oil pipelines, offshore production platforms, fuel storage tanks, well linings.
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT85904921T ATE50603T1 (en) | 1984-10-01 | 1985-09-19 | CATALYTIC POLYMER ELECTRODE FOR CATODIC PROTECTION AND CATHODIC PROTECTION SYSTEM INCLUDING THESE ELECTRODE. |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US65663484A | 1984-10-01 | 1984-10-01 | |
US77244385A | 1985-09-06 | 1985-09-06 | |
US772443 | 1985-09-06 | ||
US656634 | 1985-09-06 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0197981A1 true EP0197981A1 (en) | 1986-10-22 |
EP0197981B1 EP0197981B1 (en) | 1990-02-28 |
Family
ID=27097221
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19850904921 Expired EP0197981B1 (en) | 1984-10-01 | 1985-09-19 | Catalytic polymer electrode for cathodic protection and cathodic protection system comprising same |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0197981B1 (en) |
AU (1) | AU4960285A (en) |
BR (1) | BR8506959A (en) |
CA (1) | CA1278775C (en) |
DE (1) | DE3576174D1 (en) |
WO (1) | WO1986002106A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4957612A (en) * | 1987-02-09 | 1990-09-18 | Raychem Corporation | Electrodes for use in electrochemical processes |
GB9115184D0 (en) * | 1991-07-12 | 1991-08-28 | Jennings Winch Foundry Co Ltd | Anodes for cathodic protection |
WO1997044505A1 (en) * | 1996-05-22 | 1997-11-27 | Delektorsky Alexandr Alexeevic | Grounding anode, composition therefor and method for preparing this composition |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4381983A (en) * | 1980-06-02 | 1983-05-03 | Ppg Industries, Inc. | Solid polymer electrolyte cell |
GB2085031B (en) * | 1980-08-18 | 1983-11-16 | Diamond Shamrock Techn | Modified lead electrode for electrowinning metals |
DE3036066A1 (en) * | 1980-09-25 | 1982-05-06 | Hoechst Ag, 6000 Frankfurt | Bonding electrode to fluorine contg. copolymer electrolysis membrane - by applying electrode powder to membrane and pressing opt. with heating |
US4473450A (en) * | 1983-04-15 | 1984-09-25 | Raychem Corporation | Electrochemical method and apparatus |
-
1985
- 1985-09-19 BR BR8506959A patent/BR8506959A/en unknown
- 1985-09-19 EP EP19850904921 patent/EP0197981B1/en not_active Expired
- 1985-09-19 DE DE8585904921T patent/DE3576174D1/en not_active Expired - Fee Related
- 1985-09-19 WO PCT/US1985/001812 patent/WO1986002106A1/en active IP Right Grant
- 1985-09-19 AU AU49602/85A patent/AU4960285A/en not_active Abandoned
- 1985-09-26 CA CA000491617A patent/CA1278775C/en not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
---|
See references of WO8602106A1 * |
Also Published As
Publication number | Publication date |
---|---|
BR8506959A (en) | 1986-12-23 |
EP0197981B1 (en) | 1990-02-28 |
WO1986002106A1 (en) | 1986-04-10 |
AU4960285A (en) | 1986-04-17 |
DE3576174D1 (en) | 1990-04-05 |
CA1278775C (en) | 1991-01-08 |
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