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The corrosion behaviour of WE43 magnesium alloys using the mini cell system was studied. Voltammetry and impedance spectroscopy were applied to study on the one hand the effect of microstructure of the working electrode and on the other hand the effect of proteins in the electrolyte. Two types of alloy samples were produced (i) by permanent mould casting and (ii) by gas atomization followed by extrusion. The results showed that the microstructure was strongly influenced by the production process. The extruded samples showed an improved homogeneity of phase distribution compared with cast samples as it was aimed for. Due to increased homogeneity it was expected to find higher corrosion resistance. However, the electrochemical results are contradictory and suggest an additional phase in the extruded microstructure. Using energy dispersive X-ray spectroscopy (EDX) the secondary magnesium rare earths (RE) phase of extruded samples showed differing composition than of cast samples as well as additional oxide phases. After the samples were electrochemically investigated in cell medium with and without fetal calf serum (FCS), an impact of FCS was detected in voltammetry due to the length of the polarisation curve. As the tip of the mini cell in contact with the working electrode is small, developing gases tend to spread on the working electrode and break the contact of liquid to the counter electrode; which results in disrupting the current flow. This effect was more pronounced when rising the voltage and was found reduced when using electrolytes with FCS. Impedance spectra were slightly deformed by FCS, seen as a kinetic effect but not as a basic differing corrosion reaction. The insight into the effects of FCS was provided by the mini cell system as this system enables to collect entire series of measurements. In contrast of two single measurements, those series reflected the slight difference caused by FCS. The focus of the electrochemical corrosion study was set on the first half hour of immersion.
Statement of problems: Computer-aided design/computer-assisted machining systems offer the possibility of fabricating restorations from one machinable ceramic block. Whether multishaded blocks improve esthetic results and are a viable alternative to individually stained ceramics has not been fully determined.
Purpose: The aim of this investigation was to examine the effect of multishaded blocks on the esthetic appearance of all-ceramic CEREC crowns and compare these crowns with single-shade and stained restorations.
Material and methods: Ten subjects were included in this study. For each subject, 6 different crowns were milled with the use of a CEREC machine. One crown was milled from each of the following machinable ceramic materials: CEREC Vitablocs Mark II in classic colors; Vitablocs Mark II in 3D-Master colors; Vitablocs Mark II in either classic or 3D-Master colors, with additional staining; Megadenta Bloxx multishaded; Mark II experimental multilayer; and an experimental multilayer leucite ceramic. Three independent examiners assessed the esthetic appearance of crowns fabricated to match each subject's anterior tooth shade. A scale of 1 to 6 was used to score the shade match and esthetic adaptation of each crown, with 1 representing excellent characteristics and 3.5 serving as the threshold for clinical acceptability. The examiners' scores were averaged, and the mean values were analyzed with the Wilcoxon signed rank test (P<or=.05).
Results: Only individually stained Mark II restorations achieved a mean score below the threshold of 3.5 for all 10 subjects. These restorations were significantly more esthetic (P<or=.05) than restorations fabricated from all other materials except the Mark II experimental multilayer ceramic. The second best results were obtained for crowns made from single-shaded Mark II 3D-Master blocks: 6 out of 10 restorations were scored below 3.5. Two of the layered materials (Mark II experimental and Bloxx) followed with 5 acceptable restorations out of 10.
Conclusion: Within the limitations of this study, the results provide no evidence that multicolored machinable ceramics improve the esthetics of all-ceramic crowns.
Mg and Mg alloys are becoming more and more of interest for several applications. In the case of biomaterial applications, a special interest exists due to the fact that a predictable degradation should be given. Various investigations were made to characterize and predict the corrosion behavior in vitro and in vivo. Mostly, the simple oxidation of Mg to Mg2+ ions connected with adequate hydrogen development is assumed, and the negative difference effect (NDE) is attributed to various mechanisms and electrochemical results. The aim of this paper is to compare the different views on the corrosion pathway of Mg or Mg alloys and to present a neglected pathway based on thermodynamic data as a guideline for possible reactions combined with experimental observations of a delay of visible hydrogen evolution during cyclic voltammetry. Various reaction pathways are considered and discussed to explain these results, like the stability of the Mg+ intermediate state, the stability of MgH2 and the role of hydrogen overpotential. Finally, the impact of MgH2 formation is shown as an appropriate base for the prediction of the degradation behavior and calculation of the corrosion rate of Mg and Mg alloys.
Bioresorbable materials are under investigation due to their promising properties for applications as implant material. This study is about the degradation and bioactivity behaviour of magnesium foils, which allegorize dental membranes. The degradation behaviour including pitting corrosion during immersion tests can be precisely observed using micro-computed tomography. Using the bioactivity test according to Kokubo, it is shown that magnesium has strong Ca-phosphate layer formation correlated with high degradation. Therefore, magnesium foils appear to hold a great potential for bone implant application.
The bond between methacrylic polymer adhesives and dental restoratives is not perfect and may fail either in the short or in the long term. This study aims to evaluate the effects of particle incorporation in a self-etch model adhesive on mechanical and physical properties that are relevant during application and service. Filled adhesives containing 5, 10, 15 or 25 wt% glass fillers were compared to their unfilled counterpart in terms of water sorption and solubility; viscosity and dynamic viscosity during polymerization were recorded using rheological measurements and compared to FTIR analysis of the real-time degree of cure. Elastic modulus and ultimate tensile strength measurements were performed in uniaxial tension; the energy to fracture was used to calculate the fracture toughness of the adhesives. Finally, the experimental adhesives were applied on dentin substrate to test the bond strength using the microtensile test. Results showed that the incorporation of 5–10 wt% nanofiller to self-etching dental adhesives is efficient in accelerating the polymerization reaction and increasing the degree of cure without compromising the film viscosity for good wettability or water sorption and solubility. Fillers increased the elastic modulus, tensile strength and fracture toughness to a plateau between 5 and 15 wt% filler concentration, and despite the tendency to form agglomerations, active crack pinning/deflection toughening mechanisms have been observed. The bond strength between resin composite and dentin was also improved when adhesives with up to 10 wt% fillers were used, with no additional improvements with further packing. The use of fillers to reinforce dental adhesives may therefore be of great practical benefit by improving curing and mechanical properties.
The characterization of oxygen diffusion zone in titanium and the effect of this zone on macroscopic properties are still of high interest for a base to predict and to enhance life time of titanium and titanium alloy components. The aim of this study was to contribute to the understanding of the impact of oxygen on fatigue properties of oxygen diffusion hardened Ti and Ti alloys. Oxygen diffusion hardening implies two process steps, first the oxidation of the surface and secondly the diffusion of oxygen into metal matrix. Due to the one-step treatment used in this study the oxidation step could take place easily avoiding scaling and grain boundary diffusion. In spite of this precaution, the fatigue properties in the present study were found to be decreased after the performed oxygen diffusion hardening. The reason for the reduction of mechanical properties were claimed to be oxide clusters on the surface acting as crack initiation sites. Comparison and discussion with literature revealed varying partially contradictory fatigue results. Therefore precise analysis of the fatigue failure is necessary as a base for further development of the oxygen diffusion hardening.
A proposal for the classification of dental alloys according to their resistance to corrosion
(2007)
Objectives
The purpose of this study was to establish a method to compare and classify dental alloys in relation to their resistance to corrosion.
Methods
Alloy samples and pure metal samples were prepared and tested in chemical and electrochemical corrosion according to ISO 10271. For electrochemical test, the rest potential versus time and a potentiodynamic scan were recorded. After chemical corrosion test, the ions released were analyzed by ICP (induced coupled plasma) spectroscopy.
Results
High gold alloys had a similar polarization curve than gold. The same effect was observed for Pd–base alloys, their curves were similar to the one of palladium. The ions released during chemical corrosion were non-precious metallic ions. Thereby Ni–Cr alloys were found to release the most ions. Au–Pt alloys showed the highest release of ions compared with other precious alloys but low compared with Ni–Cr. Electrochemical corrosion was more aggressive than chemical corrosion and every type of elements was etched, the higher the precious metal content, the higher the resistance to corrosion of the alloy.
Discussion
Using the recorded data, a classification system for electrochemical corrosion was developed and discussed to judge the results. Hereby were gold and zinc used as reference materials. The applied classification system defines five classes and it is proposed that alloys of class V are not acceptable. For chemical corrosion resistance, three classes were distinguished according to the quantity of metallic ions released and it is proposed that class III (100–1000 μg/cm2 week) is not acceptable. Palladium and Pd–base alloys showed a higher electrochemical and chemical corrosion resistance than gold.