A'/> Development and microstructure characterization of single and duplex nitriding of UNS S31803 duplex stainless steel
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Development and microstructure characterization of single and duplex nitriding of UNS S31803 duplex stainless steel

机译:单层和双面氮化的开发和微观结构特征,UNS31803双相不锈钢

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Abstract In this work, the development of a duplex nitriding (DN) surface treatment combining High Temperature Gas Nitriding (HTGN) and Low Temperature Plasma Nitriding (LTPN) is reported. The microstructure and hardness variation of the duplex treated steel is compared with the properties obtained during single HTGN and single LTPN of UNS S31803 stainless steel. Single LTPN of UNS S31803 was carried out in an Active Screen Plasma Nitriding reactor, at 400°C for 20h, in a 75% N2+25% H2 atmosphere. Single HTGN of UNS S31803 was carried out at 1200°C, under a 0.1MPa high purity N2 gas atmosphere, during 8h. The developed duplex nitriding (DN) surface treatment consists of a combination of both, HTGN and LTPN treatments, carried out in the same conditions described above. The microstructure of the as received material was composed by ferrite and austenitic stringers, aligned in the rolling direction. The results showed that LTPN of the UNS S31803 duplex stainless steel promotes the formation of a duplex modulated structure composed by 2.5μm thick, 1510±52HV hard, expanded ferrite (αN) regions, and 3.0μm thick, 1360±81HV hard, expanded austenite (γN) regions on ferrite and austenite grains, respectively. Intense coherent ε-Fe3N nitride precipitation inside expanded ferrite was observed. ε-Fe3N nitrides precipitated with an orientation relationship [111] αN//[120] ε-Fe3N, leading to increased microhardness of the expanded ferrite regions. After the first step of the duplex nitriding treatment (HTGN) a 550μm thick, 330HV hard, nitrogen rich, fully austenitic layer formed at the surface of the specimens, by transformation of ferrite stringers into austenite. The second nitriding step (LTPN) led to the formation of a homogeneous expanded austenite layer, 1227±78HV on top of the thick fully austenitic layer, formed during the first step. The duplex treatment resulted in a more homogeneous, precipitate-free, microstructure and a better transition between the mechanical properties of the hardened outermost layer and the softer substrate. Highlights ? LTPN of 31803 DSS forms a nitrided layer composed by expanded γN and αN phases. ? During LTPN, ε-Fe3N nitrides precipitate in αN with
机译:<![CDATA [ 抽象 在这项工作中,一个双工氮化的发展(DN)的表面处理组合高温气体渗氮(HTGN)低温报道离子渗氮(LTPN)。双面处理的钢的显微组织和硬度变化比较了单HTGN期间获得和UNS S31803不锈钢的单一LTPN属性。 UNS S31803的单LTPN物在活性屏离子渗氮反应器中进行,在400 ℃20 小时,在75%的N2 + 25%H 2气氛。 <:HSP SP = “0.25”/ CE>℃,下一个0.1 兆帕高纯度Ñ 2 气气氛下,在8 小时。所开发的双工氮化(DN)的表面处理是由两者的组合的,HTGN和上述LTPN处理,在相同的条件下进行 所述所接收材料的显微组织是由铁素体和奥氏体桁条,在滚动方向上排列构成的。表明,UNS S31803的LTPN双相不锈钢的结果促进了2.5组成的双链体调制结构的形成微米厚,1510 ± 52 HV硬,膨胀铁氧体(αN)区,和3.0 微米厚,1360 ± 81 HV硬,膨胀奥氏体(γñ)上的铁素体和奥氏体晶粒,分别的区域。激烈相干ε - 铁 3 观察到膨胀的铁素体内部Ñ氮化物沉淀。 ε - 铁 3 Ñ氮化物与取向关系[111]α沉淀的N- // [120]ε - 铁 3 N,从而增加所述膨胀铁氧体区的显微硬度。双工氮化处理(HTGN)的第一个步骤后的550 微米厚,330 HV硬,富氮气,完全奥氏体层形成在试样的表面上,由铁素体桁条转变成奥氏体。第二氮化工序(LTPN)导致了均匀的扩张奥氏体层的形成中,1227 ± 78 HV在厚完全奥氏体层,在第一步骤中形成的顶部。双面处理导致更均匀的,无析出,微观结构和硬化最外层的机械性能和较软的衬底之间的更好的过渡。 亮点 <?CE:对ID = “P0005” 视图= “所有”> 31803 DSS的LTPN形成由扩大γ构成的氮化层ñ 和α名词 期间LTPN,ε - 铁 3 ñ氮化物沉淀在α Ñ使用

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