The pitting corrosion of three duplex steels (DSS), SAF2205, SAF2507, Z3CN20.09M thermally aged at 350 - 500 ℃ for 5500 h was investigated by the means of electrochemical techniques. The pitting potential (Ep) of thermally aged Z3CN20.09M specimens decreased with increasing of ageing temperature, however, the Ep of SAF2205 and SAF2507 thermally aged specimens decreased first and reached the lowest value at 450 ℃ and then increased slightly. The electrochemical impedance spectroscopy results are coincident with the potentiodynamic polarisation testing results. The variation in the charge transfer resistance of specimens coincided with the Ep values. There is little influence of low temperature (below 350 ℃) on resistance to pitting of SAF2205 and SAF2507 DSS. But, the pitting resistance of them degrades drastically ageing at higher temperature above 450 ℃. The deterioration in pitting resistance of thermally aged DSS specimens mainly attributes to the precipitation of Cr-rich α′ phases which affected by temperature markedly. At the range of 350 -500 ℃, the temperature the higher, the precipitation of Cr-rich α′ phases the more. The formation of G phases and the healing process during the long thermal ageing at 500 ℃ is the other reasons for the change in pitting resistance.

An in vitro experiment was conducted to study the effects of chitosan on the secretion of cytokines and expression of inducible nitric oxide synthase mRNA in peritoneal macrophages of broiler chicken. In the experiment, peritoneal macrophages were incubated for 24 h in culture medium supplemented with 0 (control), 40, 80, 160 and 320 µg/mL chitosan. The results showed that chitosan tended to increase quadratically the levels of interleukin-1 (P = 0.093) and interleukin-2 (P = 0.106) in the culture fluid of peritoneal macrophage. Chitosan also significantly enhanced inducible nitric oxide synthase mRNA expression of peritoneal macrophage in a quadratic dose-dependent manner (P < 0.05) and tended to promote quadratically the secretion of nitric oxide (P = 0.053) and inducible nitric oxide synthase (P = 0.157) in peritoneal macrophages. This result implied that one of the mechanisms by which chitosan modulated immune functions in chickens might be chitosan activating expression of inducible nitric oxide synthase and then improving the secretion of nitric oxide.