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Maruthamuthu, S. et al. - Teesside's Research Repository

Maruthamuthu, S. et al. - Teesside's Research Repository

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Formation of CuO at the m<strong>et</strong><strong>al</strong> surface is the critic<strong>al</strong> step for the occurrence of stress<br />

corrosion cracking (SCC) that was noticed on XRD which supports with the observation<br />

made by Mori <strong>et</strong> <strong>al</strong> (2005).<br />

The present study supports the observation made by Pope <strong>et</strong> <strong>al</strong>., (1984) who<br />

suggested that many organisms form NH3 from the m<strong>et</strong>abolism of amino acids. These<br />

NH4 ions in solution may play a role in the corrosion of copper <strong>al</strong>loys. Nitrogenase<br />

enzyme is the major causative factor for the production of ammonia (Smith <strong>et</strong> <strong>al</strong>., 1999).<br />

Nitrogenase works at room temperature where nitrogen gas requires reduced ferredoxin<br />

or flavodoxin and ATP as substrates. Reduced ferredoxin or flavodoxin transfers<br />

electrons to the azoferredoxin. At the expense of energy from ATP hydrolysis the<br />

potenti<strong>al</strong> of redox groups of the enzyme is lowered further and fin<strong>al</strong>ly a super-reduced<br />

molybdoferredoxin is formed, which binds N2 and reduces it stepwise to ammonia. The<br />

binding of the dinitrogen molecule occurs probably by insertion into a m<strong>et</strong><strong>al</strong>-hydride<br />

bond involving molybdenum (Gottssch<strong>al</strong>k, 1985). A MO = N-NH2 group functions<br />

probably form as an intermediates. Only the azoferredoxin component of nitrogenase has<br />

ATP-binding sites and ATP hydrolysis is primarily associated with the formation of a<br />

super-reductant. Using cell-free nitrogenase preparations, the reduction of N2 has been<br />

found to be coupled to the hydrolysis of an enormous amount of ATP, in the order of 16<br />

ATP per N2.<br />

N2 + 6H + 16 ATP 2NH3 + 16 ADP +16 Pi<br />

It is <strong>al</strong>so well known that iron sulphate is a good passivator for cupronickel,<br />

which adsorbs on the m<strong>et</strong><strong>al</strong> surface and improves passivity. Some anodic spots on the<br />

m<strong>et</strong><strong>al</strong> surface will be affected by ammonia and undergo pitting corrosion. AFM study<br />

supports the observation made in SEM and reve<strong>al</strong>s that the formed pit depth was in the<br />

range of 1000 nm within 5 days. Subsequently the ammonic<strong>al</strong> solution enhances the<br />

attack at the grain boundaries and accelerates intergranular corrosion without any stress.<br />

It concludes that Bacillus sp. may encourage intergranular attack without any stress in<br />

cooling water system. The mechanism has been explained in figure 14. When the <strong>al</strong>loys<br />

stressed in tension is <strong>al</strong>so exposed to a corrosive environment, the ensuring loc<strong>al</strong>ized<br />

15

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