Study of Microstructure and Binder Removal in an Additive-manufactured Composite Sample

2026

Closed access Metadata (CSL-JSON)
DOI 10.52209/1609-1825_2026_2_35
Data confidence 70 medium
How this score is calculated

It is built from checkable properties of the record itself: whether the article has a DOI, how many independent sources confirmed its data, whether the required fields are filled in, and how recent the latest confirmation is. Disagreement between sources and a missing identifier lower it. A value of 80 or above means the record was published without further checking; 60 to 79 means it is published at reduced confidence, with a manual check advisable. A record verified by an editor by hand is never pushed below 90 by a recalculation. This scores our data about the article, not the article itself.

Abstract

The application of a specially developed metal composite material using LDPE polymer as a binder in additive technology is described. Nitrogen environments can facilitate the formation of chromium nitride (Cr2N), particularly at temperatures between 500-600°C, adversely affecting the material's corrosion resistance. Following binder removal, the sintering process involves heating the loosely packed particles to a temperature between 70-90% of the metal powder's melting point, facilitating the powder's dense fusion and consolidation. In the metallographic study, the austenitic grain structure was shown, and the average size was 7±3 μm. Using this raw material in additive technology, a sample was developed and annealing and ripening processes were carried out in a hydrogen atmosphere up to 1387°C based on the removal of the binder in the developed sample. Complete degradation of the polymer was achieved at 500°C, with residual mass percentage (R) analysis from TGA curves revealing 94.5% steel powder, which corresponds to the expected 94.2% mass composition. Phase analysis showed the presence of an austenitic phase, which confirmed that treatment in a hydrogen-reducing atmosphere effectively protected the samples from oxidation and additional impurities. The uncontrolled cooling rate was quite slow (1-2°C/min), which allowed the powder to continue growing until it reached the recrystallization point. As a result of the microstructure analysis of the prepared sample, a level of 250 MPa and a nano-indentation hardness of 4.87 GPa were achieved. Density after sintering is 91-93%.