Microbiologically influenced corrosion can cause pitting, de alloying, enhanced erosion corrosion, enhanced galvanic corrosion, stress corrosion cracking, and hydrogen embrittlement. MIC has been documented to take place in seawater, fresh water, distilled / de mineralized water, hydrocarbon fuels, process chemicals, foods, soils, human plasma, saliva, and sewage.
Microbiologically influenced corrosion can cause pitting, de alloying, enhanced erosion corrosion, enhanced galvanic corrosion, stress corrosion cracking, and hydrogen embrittlement. MIC has been documented to take place in seawater, fresh water, distilled / de mineralized water, hydrocarbon fuels, process chemicals, foods, soils, human plasma, saliva, and sewage.
Copyright:
Attribution Non-Commercial (BY-NC)
Available Formats
Download as DOC, PDF, TXT or read online from Scribd
Microbiologically influenced corrosion can cause pitting, de alloying, enhanced erosion corrosion, enhanced galvanic corrosion, stress corrosion cracking, and hydrogen embrittlement. MIC has been documented to take place in seawater, fresh water, distilled / de mineralized water, hydrocarbon fuels, process chemicals, foods, soils, human plasma, saliva, and sewage.
Copyright:
Attribution Non-Commercial (BY-NC)
Available Formats
Download as DOC, PDF, TXT or read online from Scribd
corrosion that is caused by the presence and activities of microorganisms — that is, organisms that cannot be seen individually with the unaided human eye, including micro algae, bacteria, and fungi [4] . Microbiologically influenced corrosion can cause various forms of localized corrosion, including pitting, de alloying, enhanced erosion corrosion, enhanced galvanic corrosion, stress corrosion cracking, and hydrogen embrittlement. As a result of MIC, corrosion can occur at locations where it would not be predicted, and it can occur at very high rates. All engineering alloys, with the exception of titanium and high chromium – nickel alloys, have been reported to undergo MIC. Furthermore, MIC has been documented to take place in seawater, fresh water, distilled/de mineralized water, hydrocarbon fuels, process chemicals, foods, soils, human plasma, saliva, and sewage. Although sulfate - reducing bacteria (SRBs), active only in anaerobic (oxygen - free) environments, are a very common cause of corrosion and have been extensively studied, MIC can also be caused by other types of microorganisms — for example, Thiobacilli [sulfur - oxidizing bacteria (SOB), which oxidize sulfur compounds to sulfuric acid] and other acid - producing microorganisms, including both bacteria and fungi. Microbes can adhere to metal surfaces forming a bio film, consisting of a community of microorganisms, leading to corrosion. When the acidic products of bacterial action are trapped at the bio film – metal interface, their impact on corrosion is intensified. Although iron does not corrode appreciably in de aerated water, the corrosion rate in some natural de aerated environments is found to be abnormally high. These high rates have been traced to the presence of sulfate - reducing bacteria (e.g., Desulfovibrio desulfuricans ). Their relation to an observed accelerated corrosion rate in soils low in dissolved oxygen was first observed by von Wolzogen The bacteria are curved, measuring about 1 x 4 µm, and are found in many waters and soils. They thrive only under anaerobic conditions in the pH range of about 5.5 – 8.5. Certain varieties multiply in fresh waters and in soils containing sulfates, others flourish in brackish waters and seawater, and still others are stated to exist in deep soils at temperatures as high as 60 – 80 °C
Sulfate - reducing bacteria easily reduce
inorganic sulfates to sulfides in the presence of hydrogen or organic matter, and they are aided in this process by the presence of an iron surface. The aid that iron provides in this reduction is probably to supply hydrogen, which is normally adsorbed on the metal surface and which the bacteria use in reducing SO4 For each equivalent of hydrogen atoms they consume, one equivalent of Fe² enters solution to form rust and FeS. The bacteria, therefore, probably act essentially as depolarizers.
A possible reaction sequence can be outlined
as follows:
Anode: 4Fe → 4Fe2 + 8e‾
(7.7) Cathode: 8H2O + 8e‾ → 8Hads on Fe +8OH‾ (7.8)
formed in the proportion of 3 moles to 1 mole. Analysis of a rust in which sulfate - reducing bacteria were active shows this approximate ratio of oxide to sulfide. Qualitatively, the action of sulfate - reducing bacteria as the cause of corrosion in a water initially free of sulfides can be detected by adding a few drops of hydrochloric acid to the rust and noting the smell of hydrogen sulfide. In addition to the cathodic reaction listed in (7.8) , other cathodic reactions could be considered, such as the reduction of H2S: 2H2S +2e‾ → 2HS‾+H2 (7.12)
Severe damage by sulfate - reducing bacteria
has occurred particularly in oil – well casing, buried pipelines, water - cooled rolling mills, and pipe from deep water wells. Within 2 years, well water in the U.S. Midwest caused failure of a galvanized water pipe 50 mm (2 in.) in diameter by action of sulfate - reducing bacteria, whereas municipal water using similar wells, but which was chlorinated beforehand, was much less corrosive. A combination of low temperature and low humidity is one approach to controlling the growth of bacteria, but fungi may be capable of growing under such conditions Regular cleaning is a good practice to prevent bio film formation and subsequent corrosion. Chlorination is used to eliminate bacteria that cause corrosion, but this treatment can produce byproducts that are environmentally unacceptable. Aeration of water reduces activity of anaerobic bacteria since they are unable to thrive in the presence of dissolved O2 . Addition of certain biocides can be beneficial, but microorganisms are capable of becoming resistant to specific chemicals after long - term use. Eradication of microbial populations may be achieved by combining several chemicals or by increasing the concentration of a biocide