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ELSEVIER Wear186187 (1995)493496 WEAR Erosion of material used in petroleum production R. Hamzah, D.J. Stephenson *, J.E. Strutt School of Industrial and Manufacturing Science, Cranjeld University, Cranjield, Bedford MK43 OAL, UK Abstract Erosion<orrosion arising from sand production is increasingly recognised as a significant problem in petroleum production. When erosion and corrosion interact, they do so in such a complex manner that it is difficult to determine the rate of metal loss with sufficient accuracy for reliable prediction of equipment lifetimes. An experimental programme was carried out to study the interaction between the erosion and corrosion under typical petroleum production conditions. A C-Mn steel has been exposed to environments simulating wet and dry CO2 conditions. Erosion has been simulated by the introduction of sand particles (50-300 /.m) and the influence of impact angle, velocity, particle loading and temperature has been investigated. The results demonstrated that for C-Mn steels there is a significant interaction between erosion and corrosion with the rate of metal loss from pure corrosion to erosion/corrosion increasing by 2 orders of magnitude. The use of wet CO* increases the rate of metal loss by factor of 2-4. It has been shown that the metal recession rate at low velocity is dominated by the formation and removal of surface corrosion products. Keywords: Petroleum production; Erosion; Corrosion; Sand 1. Introduction Erosion+orrosion arising from sand production is increas- ingly recognised as a significant cause of equipment failure in petroleum production. It is believed that the combined results of erosion and corrosion would increase rates of metal loss. Typical examples of equipment failures such as the permanent choke and the blast joint of the production tubing shown in Fig. 1 are common forms of failure [ 11. From the experience of petroleum production in Malaysia and other parts of the world, the implementation of sand production controls, such as gravel-packing completions, and prone reservoirs may still produce sand up to 5 pounds per thousand barrels (pptb) [ 2,3]. This is equivalent to sand flux rates of 0.01 g mm-* h-’ in 1 in tubing (see Fig. 2) [ I]. With the introduction of a threshold limit of safe sand pro- duction of between 10 and 20 pptb. (0.1-0.2 g mm-* h- ’ for 2 in tubing and >0.5 g mm-* h-’ for 1 in tubing) by some companies, considerable metal loss rates may take place which may render the previously assumed safe practice as unsafe. 2. Experimental A series of experiments was conducted to determine the rates of corrosion, erosion and erosion-corrosion in dry and * Corresponding author. Elsevier Science S.A. SSDIOO43-1648(95)07127-X wet CO, environments on typical steels used in petroleum production. The autoclave shown in Fig. 3 and centrifugal erosion rig shown in Fig. 4 were used for the tests [ I]. A wet CO2 environment was introduced by feeding water and CO, gas into the test chamber and using an ultrasonic atomizer to simulate a wet gaseous environment. Mains water was used which contained typically 5 ppm oxygen. However, by forming an ultrafine mist of water droplets, rapid equili- bration with the CO, environment ensured that the activity of oxygen in the water on the surface of specimens was extremely low. This was confirmed by the corrosion scales which were greyish black, typical of ferrous carbonate films. Fig. 1. Erosion/corrosion in oilfields: (a) permanent choke; (b) production tubing. 494 R. Hamzah et al. /Wear 186-187 (1995) 493-496 g/mm_2/h. l.OE+OZ E l.OE-03 --- li_-_-~ii 1 10 100 1000 10000 LB./lOOOEBL(~~tb). _.._ + 1’ Tubing -+ 2’ TubinQ -se 3’ Tubing 9 4’ Tubing Fig. 2. Sand flux rates conversion. F”,“.C, _ ?? ?? i . L.“., d bP.c,m.n ?? ?? Fig. 3. The autoclave for corrosion test. Fig. 4. The centrifugal erosion-corrosion test rig Tests were conducted at 20 and 80 “C with a positive pres- sure inside the chamber of approximately 0.5 bar(g) achieved by controlling a regulator valve from a gas bottle supplying 99.95% purity CO, gas. Tests were carried out with exposure times of between 5 and 30 h, flux rates of 0.5, 0.1, 0.05 and 0.01 g mm-’ h- ’ and particles velocities of 20, 50, 80 and 150 m s ~ i The specimens were arranged such that the rates of metal loss at 15”, 30”, 45”, 60” and 90” impact angles could be calculated. The rates of metal loss for these tests were esti- mated by the weight loss method. 3. Results and discussion Typical erosion and erosion-corrosion rates vs. impact angle, as shown in Figs. 5 and 6, were obtained from the tests [ 11. It is clearly shown that the presence of the corrosive environment (Fig. 6) increases the rate of purely erosive metal loss (Fig. 5) by a factor of 2-4. As expected, the rate of metal loss increases with increas- ing sand flux rate. The value of velocity exponent obtained from the experiments was found to be between 2.5 and 2.9 in agreement with values obtained by previous workers [4- 61. For carbon manganese steels, at low velocities ( < 50 m SK’), the erosion mechanism is essentially domi- nated by scale formation and removal. However, as the veloc- ity of particles increases beyond 50 m s- ’ at sand flux rates above 0.5 g mm-’ h-i, the erosion process becomes domi- nated by substrate erosion. Wet CO, corrosion is generally regarded as film free at temperatures below about 40-60 “C. However, the erosion results indicate that the corrosion products do form even at 20 “C. The corrosion products believed to form in wet CO, between 20 and 80 “C are those of ferrous bicarbonate and ferrous carbonate [ 7-91. At these temperatures, they are soft in nature and loosely adherent to the surface. Corrosion rates are greatly reduced by the presence of a scale as ferrous ion concentrations reach their saturation level beneath the bicarbonate or carbonate layer [ 10,111, effec- tively polarising the anodic dissolution process. However, when sand particles impact the surface, the growing scale is removed locally depolarising the anodic sites and accelerat- ing the corrosion rate. This process is repeated for every particle impact on the surface. It has been found that the difference between the wet and dry erosion rates for X52 greatly exceed the rate of CO, corrosion as measured by conventional corrosion tests, indi- cating that there is a strong synergism between the erosion and corrosion processes. 4. Conclusion The following conclusions have been drawn from the experiments related to sand erosion corrosion of oilfield mate- rials and environments. R. Hamzah et al. /Wear 186-187 (1995) 493-496 495 1. 2. 3. 4. /A _f_P---- ,.OE-01 i /-- ___.___-. .__ -+_-_ I.OE-02 F ,.OE-03 II:lli 16 30 46 60 75 90 0 15 30 46 80 76 90 0 lmpol An9l.4, 9s.a. r----- --- Dw Atmos..Flux’O.O~/mm2/~T’2OC.X52 Dry Almo~..Vp-Wml9,T-ZOC.X52 Fig. 5. Erosion rates for X52. Flux. ghnm-2lh - 0.60 4 0.10 A+ 0.06 --g 0.0, (b) Fig. 6. Erosion-corrosion rates for X52 - ATTy.?OC -s co2.2oc ff co2.aoc -__ J OIAtm..W*t CO2 . ZOCIBOC.“9-~Omls.F.0.06 When sand is produced the rates of metal loss are greatly accelerated. The rate of corrosion itself is accelerated beyond that expected for the process fluid conditions as fresh metal surface is continually exposed to the corrosive environ- ment due to repeated impact by sand particles. The particles do not need to acquire high kinetic energy or velocity in order to remove the soft corrosion products as encountered in a sweet corrosion situation. At high velocity, > 50 m s- ‘, mechanical erosion of the substrate is the predominantprocess and velocity expo- nents in the range 2.5-2.9 have been measured. Acknowledgements The authors wish to thank PETRONAS, The Malaysian National Oil Company for the financial support of the project, PETRONAS Carigali Sdn. Bhd./Baram Delta Operations for making their resources available in obtaining the field data. References [ l] R. Hamzah, Ph.D. Thesis, Cranfield University. [2] H.B. Heng, Sarawak Shell Berhad: An overview of gravel-packed completions, SPE Production Eng., (May 1987) 81-88. 496 R. Hamzah et al. / Wear 186-187 (1995) 493-496 [3] R. Boni, Petronas Carigali Sdn. Bhd./Baram Delta operations, Rep. on the SIPM Progress Meet. on Sand Control and Perforating, The Hague, June 28-30, 1993. [4] I. Finnie, Erosion of surfaces by solid particles, Wear, 3 (1960) 87- 103. [5] G.P. Tilly, A two stage mechanismofductileerosion, Wear, 23 (1973) 63-79. [6] G.P. Tilly and W. Sage, The interaction of particle and material behaviour in erosion processes, Wear, 16 (1970) 447465. [7] W.F. Rogers, and J.A. Rowe, Corrosion effects of hydrogen sulphide and carbon dioxide in oil production, Proc. 4th. World Petroleum Congress, Texas, 1955, Paper 3, pp. 479-499. [8] C. De Waard and D.E. Milliams, Prediction of carbonic acid corrosion in natural gas pipelines, 1st Int. Conf on Internal and External Protection of Pipes, University of Durham, 1975, Paper Fl, [9] G.I. Ogundele and W.E. White, Some observations on corrosion of carbon steel in aqueous environments containing carbon dioxide, Corrosion-NACE, 42 (2) (Feb. 1986) 71-78. [ 101 J.O’M. Bokris, D. Drazic and A.R. Despic, The electrode kinetics of deposition and dissolution of iron, Electrochim. Acta, 4 (1961) 325- 361. [I 11 R. Jasinski, Corrosion of NIO-type steel by CO,/water mixtures, Corrosion-NACE, 43 (4) (April 1987) 214-218.
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