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Corrosion resistance of duplex stainless Steel UNS S32101 and super austenitic stainless Steel UNS NO8031 (alloy 31) was investigated in crevice conditions in a corrosive environment (saline brine, T = 60 °C, C02-flow rate 3-5 L/h, normal pressure) using electrochemical and metallographic techniques. Rectangular rubber was used to form a metal/non-metal-crevice configuration.
Potentiodynamic measurements have been carried out in order to determine critical pitting and repassivation potentials. Potentiostatic measurements at different Potentials have been performed and the dependence of pit depth on the potential applied in crevice conditions was investigated. It was shown that the repassivation potential of duplex stainless Steel S32101 coincides with its corrosion potential. Strang pitting corrosion occurred after potentiodynamic measurements with pit depths up to 100 pm. Otherwise, stainless Steel UNS NO8031 shows about 0.5 V difference between the free corrosion potential and the repassivation potential and did not show any signs of pitting corrosion after polarization measurements. Slight rouging effects have been observed. By potentiostatic measurements on duplex stainless Steel S32101 potentials slightly more positive than the corrosion Potentials causing strong pitting corrosion, and pit depths up to 650 pm were measured. Super austenitic stainless Steel UNS NO8031 did not exhibit any signs of pitting corrosion even by applying potentials much more positive than the corrosion potential.
Within the project COORAL (German acronym for ''C02 purity for capture and storage") studies on pipeline steels exposed to circulating supercritical impure C02 have been carried out. For this purpose, a loop consisting of compressors, flow meter and two autoclaves was constructed. In order to simulate the real conditions in pipelines, impurities such as H20, CO, S02, N02 and 02 were added to the C02 stream before compression. Exposure experiments were carried out with Steel specimens placed in the autoclaves. Carbon Steel L360NB, pure iron X20Cr13, X46Cr13, X2CrMnNiN22-5-2 and alloy 31 have been exposed to circulating (flow rate 4 L/min) supercritical impure C02 for one week at 60 °C and 10 MPa Surface analysis and weight loss experiments in order to determine the corrosion products and the corrosion rates showed that the impurities cause corrosion problems. Slight general corrosion by L360NB and soft iron was observed. The initiation of pitting corrosion was observed at the surfaces of the materials X20Cr13, X46Cr13, X2CrMnNiN22-5-2. No visible signs of corrosion have been observed on alloy 31.
The process chain for Carbon Capture and Sequestration (CCS) includes tubing for injection of CO2 into saline aquifers. The compressed CO2 is likely to contain specific impurities; small concentrations of SO2 and NO2 in combination with oxygen and humidity are most harmful. In addition, CO2 saturated brine is supposed to rise in the well when the injection process is interrupted. The material selection has to ensure that neither CO2 nor brine or a combination of both will leak out of the inner tubing. In this comprehensive paper the investigated materials range from low-alloy steels and 13% Cr steels up to high-alloy materials. Electrochemical tests as well as long term exposure tests were performed in CO2, in brine and combination of both; pressure was up to 100 bar, temperature up to 60 °C. Whereas the CO2 stream itself can be handled using low alloy steels, combinations of CO2 and brine require more resistant materials to control the strong tendency to pitting corrosion. The corrosion behavior of heat-treated steels depends on factors such as microstructure and carbon content. For different sections of the injection tube, appropriate materials should be used to guarantee safety and consider cost effectiveness.
Within the project COORAL (German acronym for 'CO2 purity for capture and storage') first studies on piping steels exposed to CO2 and artificial brine with high chloride concentration have been carried out. Corrosion behavior of martensitic Cr13 steel (1.4034) was investigated in a corrosive environment (artificial saline brine, T = 60 °C, CO2-flow rate 3 – 5 L/h, atmospheric pressure, exposure times from 1 h up to 14 days) using electrochemical and metallographic techniques. Different corrosion kinetics were observed as a function of exposure times and chloride concentration in the artificial brine. In CO2-saturated brine pitting corrosion was observed at free corrosion potential, whereas in the brine without addition of NaCl a stable passive layer built up. Predictions about corrosion mechanism are made and verified by means of surface analytical techniques.