Abstract

A low-temperature (400 °C) glow plasma nitriding layer on AISI 904L austenitic stainless steel was obtained at various NH3 pressures and studied using electrochemical method, X-ray diffraction, and scanning Kelvin probe. The pressure of NH3 dominated the microstructure of the nitriding layer. The saturation degree of γN controlled corrosion performance and microhardness. Insufficient NH3 pressure (<100 Pa) resulted in discontinuous nitride caking coverage, whereas excessive NH3 pressure (>100 Pa) facilitated the transformation of the nitriding layer to harmful nitrides (CrN) due to a localized overheating effect caused by the over-sputtering current.

Highlights

  • Austenitic stainless steels (ASSs) are employed in many industrial fields due to their corrosion resistance, ease of formability, and weld ability [1,2,3]

  • The black pitting was the cathodic sputtering damage caused by the glow discharge [20,21], and the amount of such pitting decreased with increasing NH3 pressure

  • Compared with that of the 904L ASS matrix, the microhardness of all the specimens subjected to low-temperature glow plasma nitriding (LTN) at different NH3 pressures had greatly improved

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Summary

Introduction

Austenitic stainless steels (ASSs) are employed in many industrial fields due to their corrosion resistance, ease of formability, and weld ability [1,2,3]. The corrosion resistance of ASSs in chloride solution or H2 SO4 /HF has been reported [4,5], whereas the corrosion of stainless steel in HF has received little attention. Polymer materials, such as polytetrafluoroethylene (PTFE), are more widely used in HF-related industries than stainless steel to prevent corrosion, metals are irreplaceable in some cases. The present research originated from an engineering problem in a heat exchanger in the phosphorite exploitation industry. The metal tubes of heat exchangers suffer from HF-containing solvent and mineral particle wear. Stainless steel with high surface hardness can be ideal tube materials

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