Microstructural Characterization and Mechanical Properties of L-PBF Processed 316 L at Cryogenic Temperature.

Laser powder bed fusion (L-PBF) has attracted great interest in the aerospace and medical sectors because it can produce complex and lightweight parts with high accuracy. Austenitic stainless steel alloy 316 L is widely used in many applications due to its good mechanical properties and high corrosion resistance over a wide temperature range. In this study, L-PBF-processed 316 L was investigated for its suitability in aerospace applications at cryogenic service temperatures and the behavior at cryogenic temperature was compared with room temperature to understand the properties and microstructural changes within this temperature range. Tensile tests were performed at room temperature and at -196 °C to study the mechanical performance and phase changes. The microstructure and fracture surfaces were characterized using scanning electron microscopy, and the phases were analyzed by X-ray diffraction. The results showed a significant increase in the strength of 316 L at -196 °C, while its ductility remained at an acceptable level. The results indicated the formation of ε and α martensite during cryogenic testing, which explained the increase in strength. Nanoindentation revealed different hardness values, indicating the different mechanical properties of austenite (γ), strained austenite, body-centered cubic martensite (α), and hexagonal close-packed martensite (ε) formed during the tensile tests due to mechanical deformation.

A novel method for producing electron transparent films of interfaces between cells and biomaterials.

Transmission electron microscopy (TEM) investigations of intact interfaces of cells and brittle biomaterials have proven difficult using common TEM preparation techniques. This paper describes a technique to fabricate thin sections for TEM investigation of intact interfaces between human monocytes and sintered hydroxylapatite by the use of focused ion beam (FIB) microscopy. The interfaces were examined using energy filtered TEM.

A comparative study of the bioactivity of three materials for dental applications.

OBJECTIVES: The aim of this work was to investigate the in vitro bioactivity of two different experimental dental luting cement formulations based on calcium aluminate (CA) in comparison with glass ionomer cement (GIC). One of the CA-based formulations was a hybrid between CA and GIC. METHODS: Samples were submerged in phosphate buffered saline and stored at 37 degrees C for four periods of time: 1 h, 1 day, 7 days and 4 weeks. After storage the samples were analyzed in order to investigate if a surface layer of hydroxyapatite had formed. The analysis techniques used included grazing incidence X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy and transmission electron microscopy. RESULTS: Both the CA-containing formulations were found to be bioactive. The highest degree of bioactivity was found on the sample with only CA as active substance. A relatively thick and totally covering layer was already formed after 24 h. On the hybrid material hydroxyapatite was found after 7 days. The GIC showed no bioactivity during the test period. SIGNIFICANCE: The utilization of a bioactive material for tooth restorations will give an opportunity for remineralization and a natural and durable seal of the tooth-material interface. Materials based on CA exhibit bioactivity.

Formation and adhesion of biomimetic hydroxyapatite deposited on titanium substrates.

This study has been carried out to investigate the bioactivity of rutile and to deposit hydroxyapatite (HA) on heat-treated titanium through a biomimetic method. Biomimetic deposition of HA has gained large interest because of its low deposition temperature and good step coverage; however, it demands a substrate with bioactive properties. Commercially pure titanium is not bioactive but it can acquire bioactive properties through various surface treatments. In the present study, titanium plates were heat-treated at 800 degrees C to achieve rutile TiO(2) surfaces. These samples were immersed in a phosphate-buffered saline solution for seven days in order to deposit a HA layer on the surface. The rutile TiO(2) surfaces were found to be highly bioactive: after seven days of immersion, a layer of HA several micrometers thick covered the plates. The HA surfaces were confirmed by electron microscopy and X-ray diffraction. A scratch test was used to assess the adhesion of the HA coatings. This is a standard method to provide a measure of the coating-to-substrate adhesion and was found to be a useful method to test the thin HA coatings deposited on the bioactive surfaces. The critical pressure of the layer was estimated to be 2.4+/-0.1GPa.