Title of article :
Effects of Molybdenum Additions on the Structure, Depth, and Austenite Grain Size of the Case of Carburized 0.13% Carbon Steels
Author/Authors :
Shorowordi، Kazi Md. نويسنده , , Bepari، Md. Mohar Ali نويسنده ,
Abstract :
Carbon (0.13%) steel samples containing about 0.48% molybdenum (Mo) singly and in combination with nickel (Ni) were carburized in a natural Titas gas atmosphere at a temperature of 1223 K (950 °C) and at a pressure of about 0.10 MPa (15 psia) for time periods ranging from 1-4 h followed by slow cooling in the furnace. Their microstructure was studied by optical microscopy. The austenite grain size of the case and the case depths were determined. It was found that Mo and Ni alone and in combination decrease the thickness of the cementite network near the surface of the carburized case of the steels. However, Ni is found to be more effective than Mo in decreasing the thickness of cementite network. Both Mo and Ni enhance the formation of Widmanstatten cementite plates at the grain boundary and within the grains near the surface of the carburized steels. However, Ni alone is more effective than Mo in the formation of Widmanstatten cementite plates. In the presence of Ni, Mo is much more effective in the formation of Widmanstatten cementite plates than Mo in absence of Ni. It was also revealed that both Mo and Ni increased the case depth. Ni is more effective than Mo in increasing the case depth. The combined effect of Mo and Ni is much greater than that of either Mo or Ni alone in increasing case depth. Mo as Mo carbide (Mo2C) particles refined the austenite grain size of the carburized case. Ni in solution was not found to have any effect in restricting grain growth of austenite, but the presence of Ni enhances the austenite grain size refining effect of Mo in the carburized case.
Keywords :
stereochemistry , Triorganylstannyl , Aliphatic Substrates , Carbonylation , (alpha)Carbon , Cycloalkyl Halides , EWG , Neopentyl , Nitroalkanes , Nitrogen Nucleophiles , Carbanions , Phosphorus Nucleophiles , sp2 Carbons , Cumyl , Nitrobenzyl , sp3 Carbons , Heterocyclic Analogues , Radicals Intermediates , Trihalides , Photostimulated Reactions , Geminal Dihalides , Regiochemistry , Alicyclic Aliphatic Substrates , Oxygen , Sulfur Nucleophiles