S. Li et al., COMPOUND LAYER GROWTH AND COMPOUND LAYER POROSITY OF AUSTENITE PLASMANITROCARBURISED NONALLOYED STEEL, Surface & coatings technology, 71(2), 1995, pp. 112-120
Compound layer growth and compound layer porosity of an austenite plas
ma nitrocarburised slowly cooled AISI 1020 steel sample were studied b
y controlling the plasma nitrocarburising atmosphere with nitrogen, hy
drogen and methane content in the following proportions: 25 vol.% N-2,
73.25 vol.% H-2, 1.75 vol.% CH4 at 600 degrees C. During the initial
stage of plasma nitrocarburising, highly porous surface structures are
formed similar to those described as ''the open structure of a piece
of coral'' observed in salt bath nitrocarburising. For a 9 min treated
sample a triple layer composed of cementile, compound layer and nitro
gen austenite is formed, which further develops into epsilon iron nitr
ide containing a compound layer and the dissociated nitrogen austenite
sublayer. Porosity is mainly nucleated and grows at the grain boundar
ies, the carbon-enriched region and places where alpha-iron forms. The
structures of quenched and annealed samples were also examined. Pure
epsilon compound top layer can be retained after quenching. This layer
is unstable at this gas composition and transforms to gamma', alpha-i
ron (and Fe3C) containing epsilon during slow cooling. Annealing enhan
ces the core property of the plain carbon steel by transforming the ma
rtensite and residual nitrogen austenite into bainite.