The purpose of this study is to investigate the electrochemical properties of Fe44Cr16Mo16C18B6amorphous alloy coating fabricated using high velocity oxygen fuel (HVOF) technology in 2.0M HCl and NaOH solution at room temperature(25°C). Based on the potentiodynamic polarization curves and Electrochemical Impedance Spectroscopy(EIS) testing results of coating in aqueous solutions of HCl and NaOH, the corrosion resistance of Fe44Cr16Mo16C18B6amorphous alloy coating in HCl solution was superior to that in NaOH solution. The icorrwas 1.487×10-5A·cm-2in HClsolution and 1.107×10-4A·cm-2in NaOH solution, while the Rtreach to 5.789×104Ω·cm2and 9780Ω·cm2, respectively. On the other hand, these corrosion phenomenon could be better interpreted by R(Q(R(RQW)))(RL) and R(RL)(Q(R(CW))) equivalent circuit model, which were different from that of other Fe-based amorphous alloys in HCl and NaOH solution, respectively.

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Various structure scales at the surface of SS400 hot rolled strip were fabricated by heat treatment processes involving different temperatures. A simulation about the effect of various temperatures on the oxide scale structure during the coiling process was carried out. The structure and corrosion behavior of different oxide scales formed at the surface of hot rolled strip were investigated in sodium bisulfite (NaHSO3) solution by scanning electron microscope (SEM), X-ray diffraction (XRD), polarization curves and electrochemical impedance spectroscopy (EIS). The scale prepared at 550 °C is mainly composed of one layer of Fe3O4 phase. The scales prepared at 600 °C and 700 °C consist of the outer thin Fe2O3 layer and the inner (Fe3O4+Fe particles) layer. The scale prepared at 650 °C is mainly composed of Fe3O4 phase as well as a spot of Fe2O3 phase. The thickness of scale prepared at 650°C is observed to be more homogeneous than that of other scales and the bonding between the scale and substrate is found to be very strong. The experimental results clearly reveal that the hot rolled strip with scale prepared at 650 °C exhibits the most excellent corrosion resisting property in 0.01 mol/L NaHSO3 solution.

A series of wedge shape Fe24+XCo24-XCr15Mo14C15B6Y2 (x=0,2,4,6,8) samples were prepared by copper mold suction casting method. The effects of high Co contents on glass forming ability (GFA) and mechanical properties of Fe24+XCo24-X Cr15Mo14C15B6Y2 bulk metallic glasses (BMG) were investigated, respectively. The glass forming ability of bulk amorphous Fe24+XCo24-XCr15Mo14C15B6Y2 (x=0,2,4,6,8) and Fe41Co7Cr15Mo14C15B6Y2 alloys have been researched. Simultaneously, the thermal conductivity parameters of those alloys were tested. The maximum thickness of amorphous region of wedge-shaped samples are dm =7.80 mm for Fe28Co20Cr15Mo14C15B6Y2, dm =7.10 mm for Fe41Co7Cr15Mo14C15B6Y2 and the thermal conductivity are λ=7.11 w.m-1.k-1 and 7.19 w.m-1.k-1, the thermal diffusivity are α=1.875 mm2/s and 1.905 mm2/s for Fe28Co20Cr15Mo14C15B6Y2 and Fe41Co7Cr15Mo14C15B6Y2 BMGs, respectively. The glass forming ability of Fe28Co20Cr15Mo14C15B6Y2 alloy is bigger than that of well known Fe41Co7Cr15Mo14C15B6Y2 alloy. With the change of Co content, the Vickers hardness of Fe24+XCo24-XCr15Mo14C15B6Y2 (x=0,2,4,6,8) change from 1292 to 1322Hv.

Fe41Co7Cr15Mo14C15B6Y2(at%) bulk metallic glass was prepared by copper mold casting. Nano-crystalline Fe41Co7Cr15Mo14C15B6Y2alloys were obtained by annealing. The influence of heat treatment at different temperatures in the alloy microstructure was identified by X-ray diffraction (XRD), and a comparative study of the electrochemical corrosion behaviors of amorphous and amorphous/nanocrystalline alloys was performed by potentiodynamic polarization method and electrochemical impedance spectroscopy (EIS) in 1.5M HCI solution, and the corrosion morphologies of the samples were observed by scanning electron microscopy (SEM). The results show amorphous alloy plays excellent anti-corrosion ability than that of the heat-treated samples, and the anti-corrosion ability of amorphous/nanocrystalline alloys decrease with the increasing of heat-treatment temperature.