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Interference The stray current is direct currents flowing in the earth from a source other than that associated

with the affected pipeline. To cause corrosion on a pipeline, the stray current must flow onto a pipeline in one area flow along the pipeline to another area and leaves the pipeline. Causing corrosion at area the current leaves. Sources of stray current include: 1. Impressed current cathodic protection system. 2. DC transit system. 3. DC mining and welding. 4. High voltage DC transmission lines Stray Current from CP Installations. Impressed current CP system can cause stray current interference on adjacent pipelines depending on the location of groundbed, the location of the pipeline. Potential of the foreign pipeline will change along with the power on and off of the protected Pipeline

Reducing Stray Current Interference The first step is to determine whether the second structure is adversely affected. This is done by noting if any changes occurs in the steel-to-soil potential of the unprotected structure when the cathodic protection current is switched from off to on. If the steel-to-soil potential becomes more positive, e.g. by 50mV or more when the cathodic protection is switched on, the unprotected structure is liable to increased corrosion as a result of the operation of the protected system. Methods of reducing the interference includes: Bonds between the offending and affected pipelines. Using of galvanic anode or add T/R at point of crossing Using coatings or shields. Drainage bonds The bond resistance is made such that the foreign line potential with affecting T/R on is the same as was observed and recorded for it with the T/R off prior to the installation of the bond. In other words, the foreign line potential will not be affected by the operation of the protected .pipeline CP system

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Measurement of potential between a pipeline and a copper sulfate reference electrode (CSE) is the most frequent test performed in the corrosion industry. All discussions in this book that deal with potential measurements will be referenced to the cse Potentials reveal several things about the pipeline being evaluated. These include a general idea of the extent to which corrosion has progressed, the location of hot spots where corrosion is most severe, and the location of areas that are subject to stray current

electrolysis.

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Galvanic Series of Metals Against CSE 1. Carbon,graphite,coke: 0.30v 2. Platinum: 0 to 0.1v 3. Mill scale on steel: -0.20v 4. High silicon cast iron: -0.20v 5. Copper,brass,bronze: -0.20v 6. Mild steel in concrete: -0.20v 7. Lead: -0.50v 8. Cast iron: -0.50v 9. Mild steel (rusted): -0.20v to 0.50v 10. Mild steel (clean and shiny): -0.50v to 0.80v 11. Commercially pure aluminum: -0.80v 12. Aluminum alloy (5% Zn): -1.05v 13. Zinc: -1.10v 14. Magnesium alloy (6%AL,3%Zn,0.15%Mn): -1.60v Commercially pure magnesium: -1.75 .15

Cathodic Protection Method


Impressed Current cathodic Protection
Impressed Current: Direct current supplied by a cathodic protection system utilizing an external power source With this method, the structure is placed in an electric circuit with a direct-power supply and an anode groundbed.Current is forced to flow from the electrolyte to the structure The system usually consists of AC converter, .groundbed,Reference cell and connection cables

Impressed Current Cathodic Protection Component


T/R: convert AC to DC and supply power to the CP system. Anodebed: Transfer the current to the environment: . Reference cells and cables

Application: Current from out side source is impressed on the pipeline by using of a groundbed and a power source.
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Advantage: It can be used in high soil resistivity with large current demand.. Limitations: 1. Need power source and more maintenance work. 2. Corrosion interference can be a problem. Anode materials: 1. Silicon iron 2. Mixed metal oxide .Platinized titanium etc .3
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Applications of Impressed Current Cathodic Protection :Typical uses of impressed current are for large current requirements, particularly for bare or poorly coated structures in all electrolyte resistivities as an economical way of protecting structures having dissipated galvanic anodes to overcome stray current or cathodic interference problems for protection of large heat exchanger water boxes, oil heater-treaters, and other vessels for interiors of water storage tanks for exterior bottoms (both primary and secondary) of above ground storage tanks for underground storage tanks for underwater components of off shore structures

. for foundation piles and sheet piling, both underground and in the water

Sacrificial Anode Cathodic Protection


Application: It is by making use of corrosion cell of dissimilar metals. Advantage:
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It can be used flexibly , easy installation and less maintenance work. Limitations: 1. Small current out put,used in place where current is small. 2. Used in low soil resistivity area. Anode materials: 1. Magnesium anode 2. Zinc anode Aluminum anode .3
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Anode and cathode ratio

If the anode is relatively small, corrosion will be severe. If the anodic area is relatively large compared with the cathode, corrosion will be relatively .mild

Polarization Electrode reactions are assumed to induce deviations from equilibrium due to the passage of an electrical current through an electrochemical cell causing a change in the electrode potential. This .electrochemical phenomenon is referred to as polarization As current flow continues over time, polarization occurs at both the anode and cathode. Polarization lowers the potential difference between the anode and cathode areas and, by Ohm's Law, the current, I, drops and the corrosion rate decreases until an equilibrium is reached between :polarization and depolarizing effects. Depolarizers include dissolved oxygen microbiological activity . water flow

Depending on the type of resistance that limits the reaction rate, we are talking about three different kinds of polarization activation polarization concentration polarization and resistance (ohmic) polarization or IR Drop Lead immersed in H2SO4 Magnesium exposed to natural waters Iron immersed in a chromate solution

Zinc in H2SO4 Iron exposed to natural waters

Crevice Corrosion
Concentration cells form due to differences in metal (or dissolved gases) ion concentration in the electrolyte between two .(regions of (same) metal piece(s Metal in contact with more concentrated electrolyte becomes cathode, metal in contact with more dilute solution becomes anode and .corrodes Electrons flow from the low-oxygen area on the metal which acts as the anode to the high-oxygen .area on the metal which acts as the cathode

FIGURE 18.15 On this plate, which was immersed in seawater, crevice corrosion has occurred at the regions that were .covered by washers

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