2013
DOI: 10.1007/s10853-013-7248-2
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Nitriding behaviour of maraging steel: experiments and modelling

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Cited by 19 publications
(7 citation statements)
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“…Thermo-chemical treatment is based on the diffusion change of the chemical composition of SL in order to obtain the required functional properties of tools. SL modification processes include nitriding and sulfonitriding (Baranowska et al 2007), (Lesz et al 2010), (Małdziński et al 2010), (Ratajski et al 2009), (Cernan et al 2012), (Sato et al 2012), (Selg et al 2013). Two variants of mechanical processes combined with sulfonitriding treatment were-grinding or hard turning and slide burnishing with 130 N force, respectively.…”
Section: Tool Steelsmentioning
confidence: 99%
“…Thermo-chemical treatment is based on the diffusion change of the chemical composition of SL in order to obtain the required functional properties of tools. SL modification processes include nitriding and sulfonitriding (Baranowska et al 2007), (Lesz et al 2010), (Małdziński et al 2010), (Ratajski et al 2009), (Cernan et al 2012), (Sato et al 2012), (Selg et al 2013). Two variants of mechanical processes combined with sulfonitriding treatment were-grinding or hard turning and slide burnishing with 130 N force, respectively.…”
Section: Tool Steelsmentioning
confidence: 99%
“…A number of studies have previously employed denitriding in flowing H 2 -atmosphere of nitrided ferritic specimens. 17,25,41,4547 In most of these investigations, higher prenitriding temperatures and longer prenitriding times than in the current study were employed, e.g. prenitriding at 580 °C for 24 h with a nitriding potential of 0.104 atm −½ in Hosmani et al 45 .…”
Section: Resultsmentioning
confidence: 98%
“…This includes the excess nitrogen dissolved in the ferrite matrix due to the expansion of the ferrite matrix by the precipitate-strain field, the so-called mobile excess nitrogen; 37,38 (iii) adsorbed/segregated nitrogen: due to the usually nano-sized nature of the nitride precipitates and the corresponding, very large, coherent precipitate/matrix interfacial area, considerable nitrogen can be adsorbed at the precipitate–matrix interfaces; this is the so-called immobile excess nitrogen. 37,38 In order to quantitatively describe the nitriding process (see, e.g., Schacherl et al , 38 Meijering, 39 van Landeghem et al , 40 Selg et al , 41 and Jung et al 42 ), knowledge of the respective amounts of excess nitrogen is required. Previous analyses of absorbed nitrogen of types (i–iii) have been performed in Hosmani et al , 17 Podgurski et al , 22 Biglari et al , 25 Jack, 43 Podgurski and Davis, 44 Hosmani et al , 45 Hosmani et al , 46 Jung et al 47 .…”
Section: Introductionmentioning
confidence: 99%
“…The large volumetric misfit of nitride precipitates and ferrite matrix (see Table 1) leads to a considerable tendency for the nitrided zone to expand. However, as the nitride zone is constrained by its adherence to the (rigid) unnitrided core, high compressive (residual) macrostress is present parallel to the surface in the surface adjacent region ( Ref 24,48,78,79). Upon relaxation of the nitrided zone, e.g., by DC (Ref 24), the compressive macrostress at the surface relaxes, and may even turn to a tensile macrostress, if the relaxed region is ''on top'' of a ''freshly nitrided'' region [see Fig.…”
Section: Macro-and Microstresses/strains In the Nitrided Microstructurementioning
confidence: 99%