In vitro degradation behavior of Fe–20Mn–1.2 C alloy in three different pseudo-physiological solutions

E Mouzou, C Paternoster, R Tolouei, A Purnama… - Materials Science and …, 2016 - Elsevier
E Mouzou, C Paternoster, R Tolouei, A Purnama, P Chevallier, D Dube, F Prima
Materials Science and Engineering: C, 2016Elsevier
High manganese austenitic steels such as Fe–20Mn–1.2 C alloys are among the most
promising candidates for biodegradable stents applications due to their high strength, high
ductility and their chemical composition. In the current work, 14 day static in-vitro tests were
performed in controlled atmosphere to assess the degradation behavior in three common
pseudo-physiological solutions, ie commercial Hanks'(CH), modified Hanks'(MH) and
albumin-enriched Dulbecco's modified phosphate buffered saline (DPBS) solutions. The …
Abstract
High manganese austenitic steels such as Fe–20Mn–1.2C alloys are among the most promising candidates for biodegradable stents applications due to their high strength, high ductility and their chemical composition. In the current work, 14 day static in-vitro tests were performed in controlled atmosphere to assess the degradation behavior in three common pseudo-physiological solutions, i.e. commercial Hanks' (CH), modified Hanks' (MH) and albumin-enriched Dulbecco's modified phosphate buffered saline (DPBS) solutions. The degraded samples surfaces as well as the degradation products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR).
Degradation of material and degradation products are shown to be strongly dependent on the test medium due to the presence of different ionic species such as HCO3, CO32 −, Cl, Ca2 + or phosphate groups. In both MH and CH solutions, the increased content of HCO3 ions seems to promote MnCO3 crystal growth on sample surfaces whereas the presence of albumin and high content of phosphate ions promotes the formation of an amorphous layer rich in phosphates, iron and manganese.
Elsevier
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