Effect of thermomechanical treatment on structure and mechanical properties of Mo-bearing dual phase steel

The effects of hot rolling of a dual phase steel in the (α + γ) range on microstructure and mechanical properties was investigated by using two thermomechanical (TMT) routes. The first consisted of heating A_c3, soaking, cooling to deformation temperature in the (α + γ) range. The second comprises heating to deformation temperature in the (α + γ) range, followed by rolling and quenching. Parameters varied were temperature (with the first route) and extent of deformation (with the second). The microstructures were characterised by optical and transmission electron microscopy. The results indicate a distinct difference in the final structure and properties due to the two different TMT routes. The first TMT route resulted in a greater amount of ferrite, finer lath width of martensite, finer ferrite grain size and increased density of dislocations. The strength properties decreased, the YS/UTS ratio decreased and ductility increased with the increase in the extent and temperature of deformation. However, TMT route 2 resulted in an increase in the amount of martensite, finer ferrite grain size, decrease in the martensite lath width and increased dislocation density. The strength properties increased, YS/UTS ratio increased and ductility decreased with increase in the extent and temperature of deformation.     

In vitro and in vivo dependency of chemokine generation on C5a and TNF-alpha

Under a variety of conditions, alveolar macrophages can generate early response cytokines (TNF-alpha, IL-1), complement components, and chemotactic cytokines (chemokines). In the current studies, we determined the requirements for TNF-alpha and the complement activation product C5a in chemokine production in vitro and in vivo. Two rat CXC chemokines (macrophage inflammatory protein (MIP)-2 and cytokine-induced neutrophil chemoattractant (CINC)) as well as three rat CC chemokines (MIP-1alpha, MIP-1beta, and monocyte chemoattractant protein (MCP)-1) were investigated. Chemokine generation in vitro was studied in rat alveolar macrophages stimulated with IgG immune complexes in the absence or presence of Abs to TNF-alpha or C5a. The rat lung injury model induced by IgG immune complex deposition was employed for in vivo studies. Abs to TNF-alpha or C5a were administered intratracheally or i.v., and effects on chemokine levels in bronchoalveolar lavage fluids were quantitated by ELISA. Both in vitro and in vivo studies demonstrated the requirements for TNF-alpha and C5a for full generation of CXC and CC chemokines. In vitro and in vivo blockade of TNF-alpha or C5a resulted in significantly reduced production of chemokines. Supernatant fluids from in vitro-stimulated macrophages revealed by Western blot analysis the presence of C5a/C5adesArg, indicating intrinsic generation of C5a/C5adesArg by alveolar macrophages and explaining the higher efficiency of intratracheal vs i.v. blockade of C5a in reducing chemokine production. These results underscore the central role of both TNF-alpha and C5a, which appear to function as autocrine activators to promote CXC and CC chemokine generation by alveolar macrophages.