Effect of MgO-Cr_(2)O_(3) and Mg0-MgAl_(2)0_(4)-based refractories on refractory-steel interface reaction and cleanliness of pipeline steel

The interaction of MgO-MgAl_(2)O_(4)-based and MgO-Cr_(2)O_(3)-based refractories with X70 molten steel was studied by immersion experiments at 1560℃.The effects of immersion time(30 and 60 min)on the contents of total oxygen(TO),Al,Nb,Si,Mn,and Cr as well as the composition,number density,and size distribution of inclusions in the molten steel were investigated.The influence of the penetration and erosion degree of the molten steel to the refractory on the steel-refractory interface layer was analyzed.The results show that,at 1560℃,the MgO-MgAl_(2)O_(4)-based refractory can better control the contents of TO and the composition of molten steel compared with the MgO-Cr_(2)O_(3)-based refractory.The TO content is only 16×10^(-4) wt.%in the molten steel after reacted with the Mg0-MgAl_(2)O_(4)-based refractory at the end point of refining,4 accounting for 11.5%of that reacted with the MgO-Cr_(2)O_(3)-based refractory(139×10^(-4) wt.%).The number density of inclusions is only 14 mm^(-2),and the average size ofinclusions is only 1.31μm,with thelargest proportion of inclusions in 1-2μm(70%).The Al_(2)O_(3)-MnS-CaO complex inclusions in the original steel changed to complex inclusions dominated by Cr-Nb-Mn-S-O and MgO.Al_(2)O_(3),corresponding to the MgO-Cr_(2)O_(3)-based and MgO-MgAl_(2)O_(4)-based refractories,respectively.The MgO.Al_(2)O_(3) layer was formed at the reaction interface between MgO-MgAl_(2)O_(4)-based refractory and molten steel,which is helpful to restrict the erosion of refractories and the pollution of molten steel.The damage mechanism of the MgO-Cr_(2)O_(3)-based refractory is mainly permeation and chemical reaction,while the damage of the MgO-MgAl_(2)O_(4)-based refractory is mainlyscouring erosion.

Interfacial microstructure and properties of YG11C/42CrMo joint brazed with BCu64MnNi filler metal

Brazing hard alloy to high strength steel, incomplete atomic diffusion and excessive brittle reaction product precipitation at the faying interface are usually suffered because of incomplete understanding the process of the initial interface disappearing and diffusion layer forming and evolving. In this paper , hard alloy YG11C （ WC-11wt. %Co） and high strength steel 42CrMo were picked up as base metals and BCu64MnNi as filler metal to clarify the interfacial microstrncture evolution. The process parameters of dwell time were set as 30 s, 60 s, 120 s, and 300 s and braze temperature were set as 950 ℃, 970 ℃, 990 ℃, 1 010 ℃, the effect of which on the evolution of interfacial microstructure, tensile strength, integrated with fracture morphology analysis, were conducted. The results showed that increasing brazing temperature from 950 ℃ to 970 ℃, no signifwant difference existed in the joint interface, whereas brazed at 990 ℃, the binder phase erosion occurred, i. e. the liquid filler metal etched into Co binder phase of WC-Co base metal, which caused WC particles debonding from the base metal surface and formed an micro-anisotropic zone.. Increase temperature to 1 010 ℃, severe binder erosion happened so as to micropores appear. Through the parameters optimization, the tensile strength can reach to the maximum 589 MPa at temperature of 970 ℃. The dwell time showed similar effect on tensile strength because longer dwell time also caused erosion and porosity owing to long-time diffusion and reaction.

Interfacial Structure and Formation Mechanism of Ultrasonic-assisted Brazed Joint of SiC Ceramics with Al—12Si Filler Metals in Air

Ultrasonic-assisted brazing of SiC ceramics was performed by filling with an Al-12Si alloy at a low tem- perature of 620 ℃ in air. The interracial characteristics and formation mechanism were investigated. The joint shear strength reached 84-94 MPa using the ultrasonic time of 2-16 s. The fracture morphology showed that the fracture path initiated and propagated in the joint alloy. The thin film of amorphous SiO2 that formed on the SiC surface was non-uniformly decomposed and diffused into the liquid Al-12Si alloy under the cavitation erosion effect of ultrasound. Abnormal isolated blocks of A12SiO5 compounds formed at the interface between Al-12Si and a thicker SiO2 layer formed during the thermal oxidation treatment of the SiC ceramic. The SiO2 layer on the SiC ceramic did not hinder or impair the wetting and bonding process, and a stronger bond could form between Al-12Si and SiO2 or SiC in ultrasonic- assisted brazing.