The role of acetic acid in FeCO3 scale deposition on CO2 corrosion of API X65 carbon steel under high temperatures

Author(s):  
Bernardo Augusto Farah Santos ◽  
Rhuan Costa Souza ◽  
Maria Eduarda Dias Serenario ◽  
Eugenio Pena Mendes Junior ◽  
Thiago Araujo Simões ◽  
...  

The formation/deposition of hydrate and scale in gas production and transportation pipeline has continue to be a major challenge in the oil and gas industry. Pipeline transport is one of the most efficient, reliable and safer means of transporting petroleum products from the well sites to either the refineries or to the final destinations. Acetic acid (HAc), is formed in the formation water which also present in oil and gas production and transportation processes. Acetic acid aids corrosion in pipelines and in turn aids the formation and deposition of scales which may eventually choke off flow. Most times, Monethylene Glycol (MEG) is added into the pipeline as an antifreeze and anticorrosion agent. Some laboratory experiments have shown that the MEG needs to be separated from unwanted substance such as HAc that are present in the formation water to avoid critical conditions in the pipeline. Internal pipeline corrosion slows and decreases the production of oil and gas when associated with free water and reacts with CO2 and organic acid by lowering the integrity of the pipe. In this study, the effect of Mono-Ethylene Glycol (MEG) and Acetic acid (HAc) on the corrosion rate of X-80 grade carbon steel in CO2 saturated brine were evaluated at 25oC and 80oC using 3.5% NaCl solution in a semi-circulation flow loop set up. Weight loss and electrochemical measurements using the linear polarization resistance (LPR) and electrochemical impedance spectroscope (EIS) were used in measuring the corrosion rate as a function of HAc and MEG concentrations. The results obtained so far shows an average corrosion rate increases from 0.5 to 1.8 mm/yr at 25oC, and from 1.2 to 3.5 mm/yr at 80oC in the presence of HAc. However, there are decrease in corrosion rate from 1.8 to 0.95 mm/yr and from 3.5 to 1.6mm/yr respectively at 25oC and 80oC on addition of 20% and 80% MEG concentrations to the solution. It is also noted that the charge transfer with the electrochemical measurements (EIS) results is the main corrosion controlling mechanism under the test conditions. The higher temperature led to faster film dissolution and higher corrosion rate in the presence of HAc. The EIS results also indicate that the charge transfer controlled behaviour was as a result of iron carbonate layer accelerated by the addition of different concentrations of MEG to the system. Key words: CO2 corrosion, Carbon steel, MEG, HAc, Inhibition, Environment.


2008 ◽  
Vol 39 (6) ◽  
pp. 873-877 ◽  
Author(s):  
Peter C. Okafor ◽  
Bruce Brown ◽  
Srdjan Nesic

2008 ◽  
Vol 10 (2) ◽  
pp. 200-203 ◽  
Author(s):  
J. Amri ◽  
E. Gulbrandsen ◽  
R.P. Nogueira

2019 ◽  
Vol 156 ◽  
pp. 58-70 ◽  
Author(s):  
Amir Shamsa ◽  
Richard Barker ◽  
Yong Hua ◽  
Evgeny Barmatov ◽  
Trevor L. Hughes ◽  
...  
Keyword(s):  

2010 ◽  
Vol 42 (9) ◽  
pp. 1483-1488 ◽  
Author(s):  
Z. F. Yin ◽  
Z. Q. Bai ◽  
W. J. Zhou ◽  
Bin Li

2008 ◽  
Vol 55 (3) ◽  
pp. 130-134 ◽  
Author(s):  
Dong Liu ◽  
ZhenYu Chen ◽  
XingPeng Guo

CORROSION ◽  
10.5006/3569 ◽  
2020 ◽  
Author(s):  
MARIANA FOLENA ◽  
Richard Barker ◽  
Frederick Pessu ◽  
JOSE ANTONIO PONCIANO GOMES ◽  
Anne Neville

Based on a review of both literature and field data, it is apparent that the role of acetic acid (HAc) in oilfield brines is both extremely complex and somewhat controversial. Although it is commonly believed that the presence of this organic compound enhances both the general and the localized corrosion rate of carbon steel, HAc has recently been reported to also act as a weak general corrosion inhibitor in specific aqueous environments. These observations prompted a study into whether such behavior is apparent in a CO<sub>2</sub> top-of-line corrosion (TLC) scenario i.e. when HAc dissolves into condensed water which forms on the upper internal wall of carbon steel pipelines during wet-gas stratified flow. Four different water condensation rates/temperature TLC conditions were selected to investigate the role of HAc on both the kinetics and mechanism of carbon steel dissolution. A miniature three-electrode setup was developed to characterize the real-time TLC response through the implementation of electrochemical measurements. Surface analysis techniques (microscopy and profilometry) were also performed to complement the electrochemical results. Collective consideration of the corrosion response and condensate chemistry indicates that similar effects were observed compared to those reported in the literature for bulk aqueous environments, in that the introduction of HAc can result in either accentuation or a minimal/inhibitive effect on general corrosion depending upon the operating conditions. The minimal/inhibitive effects of HAc were apparent at a surface temperature of 20.5<sup>o</sup>C and water condensation rate of 0.5ml/m<sup>2</sup>.s as no significant increase in corrosion was observed despite a significant reduction in condensate pH being generated due to the presence of HAc. X-ray photo-electron spectroscopy analysis of the inhibited steel specimen in the presence of HAc revealed the presence of iron acetate on the steel surface which may have been at least partially responsible for the observed inhibitive effect. Extended duration experiments over 96h revealed that both general and localized corrosion are not significantly affected by HAc addition at low temperature whilst the level of degradation increases at higher surface temperature over longer periods.


Planta Medica ◽  
2009 ◽  
Vol 75 (09) ◽  
Author(s):  
FM de-Faria ◽  
A Luiz-Ferreira ◽  
ACA Almeida ◽  
V Barbastefano ◽  
MA Silva ◽  
...  

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