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The phase and composition depth distributions of a low-energy (0.7 keV), high-flux (2.5 mA/cm2) N implanted fcc AISI 304 stainless steel held at 400 °C have been investigated by step-wise Ar+ beam sputter removal in conjunction with conversion electron Mössbauer spectroscopy and x-ray diffraction (XRD). A metastable, fcc, high-N phase (γN), with both magnetic and paramagnetic characteristics, was found to be distributed in the N implanted layer generated by the low-energy, elevated temperature, implantation conditions. The magnetic γN was found to be ferromagnetic and was distributed in the highest N concentration region of the implanted layer (the top 0.5 μm) while the paramagnetic γN becomes predominant below 0.5 μm, where the N content is only slightly lower. The ferromagnetic state is linked to large lattice expansions due to high N contents (∼30 at.%) as determined by XRD and electron microprobe. The relatively uniform XRD N distribution to a depth of ∼1 μm suggests a sensitive dependence of the magnetic γN phase stability on N concentration and degree of lattice expansion. The XRD results also show that the N contents and depths depend on the polycrystalline grain orientation relative to the ion beam direction. The N was found to diffuse deeper in the (200) oriented polycrystalline grains compared to the (111) oriented grains and the N contents were significantly higher in the (200) planes relative to the (111) planes. The effect of compressive residual stresses (∼2 GPa) is considered. The scanning electron microscopy (SEM) analysis reveals quite clearly the uniform nature of the γN layers with a reasonably well defined interface between the γN layer and the substrate, suggesting uniform N contents with uniform layer thicknesses within a given grain. However, they also show significant variations in the γN layer thickness from one grain to the next along the N implanted layer, clearly supporting the XRD findings of the variation in N diffusivity with grain orientation.

We investigated the short-term (4 weeks)color stability of light-cure and dual-cure resin cements. Sixty disk-shaped test specimens of adhesive resin cement (10 × 1 mm) were prepared. One feldspathic porcelain test specimen (12 × 14 × 0.8 mm) was prepared from a prefabricated ceramic block. The feldspathic sample was placed on the resin cement disk and all the measurements were performed without cementation. Specific color coordinate differences (ΔL, Δa, and Δb), and the total color differences (ΔE) were calculated after immersion in distilled water for different periods. Data were compared using one-way analysis of variance (

CoCrMo alloys are used as orthopedic implant materials because of their excellent mechanical and corrosion properties. However, when placed in vivo, these alloys release Co, Cr, Mo ions to host tissues, which may give rise to significant health concerns over time. Nitrogen ion implantation can be used to form protective layers on the surface of CoCrMo orthopedic alloys by modifying the near surface layers of these materials. In this study, medical grade CoCrMo alloy (IS0 5832-12) was ion implanted with 60 keV nitrogen ions to a high dose of 1.9 × 10 18 ions/ cm 2 at substrate temperatures of 100, 200 and 400°C. The N implanted layer microstructures, implanted layer phases, and thicknesses were studied by a combination of Bragg-Brentano (θ/2θ) and grazing incidence (Seeman-Bohlin) X-ray diffraction (XRD and GIXRD) and crosssectional scanning electron microscopy (SEM). Atomic force microscopy (AFM) was used for roughness analysis of N implanted as well as aspolished surfaces. Static immersion tests were performed to investigate metal ion release into simulated body fluid (SBF) by electrothermal atomic absorption spectrometry (ETAAS) and inductively coupled plasma optical emission spectrometry (ICP-OES). XRD and SEM analyses indicated that the N implanted layers were ∼ 150-450 nm thick and composed of the (Co,Cr,Mo) 2+x N nitride phase and a high N concentration Co-based FCC phase, γ N depending on the substrate temperature. ETAAS analysis results showed that in vitro exposure of the N implanted surfaces resulted in higher levels of cobalt ion release into the simulated body fluid compared to the untreated, polished alloy. The higher Co release from the N implanted specimens is attributed to the nature of the implanted layer phases as well as to the rougher surfaces associated with the N implanted specimens compared to the relatively smooth surface of the untreated material. SEM analysis of N implanted and untreated specimens after immersion tests clearly indicated calcium phosphate formation on the as-polished CoCrMo alloy, indicating a degree of bioactivity of the untreated metal surface which is absent in the N implanted specimens.