Metallurgical Structures of As-Cast and Heat-Treated High-Palladium Dental Alloys

Scanning electron microscope observations and energy-dispersive spectroscopic analyses have been performed on two first-generation and two second-generation high-palladium dental casting alloys. A specimen design simulating a maxillary central incisor coping was employed to conserve metal, while providing thin and thick sections to yield a range of solidification rates. The alloys were centrifugally cast in air, following standard dental laboratory techniques; three castings were prepared for each alloy. Each casting was sectioned to produce two mirror-image specimens, and one specimen received the appropriate oxidation heat treatment, followed by a simulated full porcelain firing sequence. After metallographic polishing, specimens were examined with a scanning electron microscope. The as-cast alloys displayed multi-phase microstructures which could be explained by the rapid solidification conditions and the relevant phase diagrams. The simulated porcelain firing heat treatment caused a variety of bulk microstructural changes in the coping sections, along with formation of complex subsurface oxidation regions which were less thick for the second-generation alloys. Elemental compositions of the palladium solid solution matrix in the heat-treated alloys were in good agreement with nominal alloy compositions provided by the manufacturers. Ruthenium-rich particles found in the microstructures of three alloys are consistent with a proposed mechanism for grain refinement

Metallurgical Structures of As-Cast and Heat-Treated High-Palladium Dental Alloys

Scanning electron microscope observations and energy-dispersive spectroscopic analyses have been performed on two first-generation and two second-generation high-palladium dental casting alloys. A specimen design simulating a maxillary central incisor coping was employed to conserve metal, while providing thin and thick sections to yield a range of solidification rates. The alloys were centrifugally cast in air, following standard dental laboratory techniques; three castings were prepared for each alloy. Each casting was sectioned to produce two mirror-image specimens, and one specimen received the appropriate oxidation heat treatment, followed by a simulated full porcelain firing sequence. After metallographic polishing, specimens were examined with a scanning electron microscope. The as-cast alloys displayed multi-phase microstructures which could be explained by the rapid solidification conditions and the relevant phase diagrams. The simulated porcelain firing heat treatment caused a variety of bulk microstructural changes in the coping sections, along with formation of complex subsurface oxidation regions which were less thick for the second-generation alloys. Elemental compositions of the palladium solid solution matrix in the heat-treated alloys were in good agreement with nominal alloy compositions provided by the manufacturers. Ruthenium-rich particles found in the microstructures of three alloys are consistent with a proposed mechanism for grain refinement

X-Ray Diffraction and Scanning Electron Microscopy Analyses of a Gallium-Based Dental Restorative Alloy

Specimens of a gallium-based dental alloy were prepared with different condensation techniques, with and without the removal of a surface layer, and after aging for 2 hours at 50°, 100° and 150°C. X-ray diffraction at times ranging from 10 minutes to 1 day showed the development of the four matrix phases (ß-Sn, CuGa2, Ga28Ag72, and In4Ag9) during the setting reaction. Scanning electron microscope (SEM) examination of specimens loaded to failure revealed brittle fracture, with greater porosity for hand-condensed specimens, and provided insight into crack propagation processes. Aging increased the amount of ß-Sn in freshly prepared specimens, and removal of the Ga-rich surface layer after condensation decreased the amount of this phase. For specimens stored for 5 weeks at room temperature, aging substantially increased the amount of the CuGa2 phase but caused only moderate increases in the amount of ß-Sn

Mechanical Properties of Dendritic Pd-Cu-Ga Dental Alloys

Three Pd-Cu-Ga dental alloys with very similar nominal compositions and dendritic as-cast microstructures were selected for study: Option (Ney Dental) and Spartan (Williams/lvoclar) contain a small amount of boron, while Spartan Plus (Williams/Ivoclar) is boron-free. Bars of each alloy were tested in tension for the as-cast and simulated porcelain-firing conditions, and values of mechanical properties were measured. Fracture surfaces and microstructures of axially sectioned and etched fracture specimens were observed with the scanning electron microscope (SEM). Except for the elastic modulus, significant differences were typically found in alloy properties. Heat treatment eliminated the dendritic microstructure, decreased strength and increased ductility. Values of mechanical properties depend on the presence (orientation and distribution) of dendrites but not boron content. The amounts of casting porosity in the samples were too small to affect their mechanical properties significantly

Room Temperature Aging of Pd-Cu-Ga Dental Alloys

Specimens of three Pd-Cu-Ga dental alloys cast five years ago and subsequently stored at room temperature were reexamined and observed to have lower amounts of the eutectic constituents in the near-surface region than originally present, along with other microstructural changes. This previously unreported room temperature aging behavior of these alloys is attributed to the presence of high-diffusivity paths in the non-equilibrium ascast eutectic structures and to the essential role of the surface for the vacancy diffusion mechanism. These results may have important clinical significance for the ill vivo corrosion resistance and long-term biocompatibility of the Pd-Cu-Ga alloys

Developing a Robust Geologic Conceptual Model Using Pseudo 3-D P-Wave Seismic Reflection Data

As part of a multiscale hydrogeophysical and modeling study, a pseudo three-dimensional (3-D) seismic surveywas conducted over a contaminant plume at P area, Savannah River site (South Carolina), to enhance the existing geologicmodel by resolving uncertainties in the lithostratigraphic sequence. The geometry of the dissolved phase trichloroethylene plume, based on initial site characterization, appears to be confined to a narrow corridor within the Eocene sand overlying a clay unit approximately 25m(82 ft) below land surface. Processing the seismic data as a 3-D data volume instead of a series of closely spaced two-dimensional lines allowed for better interpretation of the target horizons, the lower clay, and the sand above the clay. Calibrating the seismic data with existing borehole geophysical logs, core data as well as vertical seismic profiling (VSP) data allowed the seismic data to be inverted from two-way travel-time to depth, thereby facilitating full integration of the seismic data into a solid earth model that is the basic part of a site conceptual model. The outcome was the production of realistic horizon surface maps that show that two channel complexes are located on the section, which are not present in the conceptual model, and that the upper and middle clays are not laterally continuous as previously thought. The geometry of the primary channel has been transposed over the map view of the plume to investigate potential relationships between the shape of the plume and the presence of the channel

Effects of Casting Conditions and Annealing on Microstructures and Vickers Hardness of Dendritic Pd-Cu-Ga Dental Alloys

Three Pd-Cu-Ga alloys with as-cast dendritic microstructures and very similar compositions, two containing less than 1 wt% boron and the third boron-free, were cast with normal bench-cooling or rapid-quenching into water. Quenched specimens were also heat treated at temperatures of 1000°, 1200°, 1500° and 1800°F that span the firing cycles for dental porcelain. Similar values of Vickers hardness were observed for all three alloys, suggesting little effect from boron on yield strength. The hardness was relatively insensitive to the experimental conditions, except for heat treatment at 1500° and 1800°F where significant softening occurred with transformation of the microstructure to Pd2Ga and the palladium solid solution

Characterization of an electron conduit between bacteria and the extracellular environment

A number of species of Gram-negative bacteria can use insoluble minerals of Fe(III) and Mn(IV) as extracellular respiratory electron acceptors. In some species of Shewanella, deca-heme electron transfer proteins lie at the extracellular face of the outer membrane (OM), where they can interact with insoluble substrates. To reduce extracellular substrates, these redox proteins must be charged by the inner membrane/periplasmic electron transfer system. Here, we present a spectro-potentiometric characterization of a trans-OM icosa-heme complex, MtrCAB, and demonstrate its capacity to move electrons across a lipid bilayer after incorporation into proteoliposomes. We also show that a stable MtrAB subcomplex can assemble in the absence of MtrC; an MtrBC subcomplex is not assembled in the absence of MtrA; and MtrA is only associated to the membrane in cells when MtrB is present. We propose a model for the modular organization of the MtrCAB complex in which MtrC is an extracellular element that mediates electron transfer to extracellular substrates and MtrB is a trans-OM spanning ß-barrel protein that serves as a sheath, within which MtrA and MtrC exchange electrons. We have identified the MtrAB module in a range of bacterial phyla, suggesting that it is widely used in electron exchange with the extracellular environment

The Center for Environmental Kinetics Analysis: an NSF- and DOE-funded Environmental Molecular Science Institute (EMSI) at Penn State

Physicochemical and microbiological processes taking place at environmental interfaces influence natural processes as well as the transport and fate of environmental contaminants, the remediation of toxic chemicals, and the sequestration of anthropogenic CO2. A team of scientists and engineers has been assembled to develop and apply new experimental and computational techniques to expand our knowledge of environmental kinetics. We are also training a cohort of talented and diverse students to work on these complex problems at multiple length scales and to compile and synthesize the kinetic data. Development of the human resources capable of translating molecular-scale information into parameters that are applicable in real world, field-scale problems of environmental kinetics is a major and relatively unique objective of the Institute's efforts. The EMSI team is a partnership among 10 faculty at The Pennsylvania State University (funded by the National Science Foundation Divisions of Chemistry and Earth Sciences), one faculty member at Juniata College, one faculty member at the University of Florida, and four researchers drawn from Los Alamos National Laboratory, Pacific Northwest National Laboratory, and Lawrence Berkeley National Laboratory (funded by the Department of Energy Division of Environmental Remediation Sciences). Interactions among the applied and academic scientists drives research approaches aimed toward solving important problems of national interest. The Institute is organized into three interest groups (IGs) focusing on the processes of dissolution (DIG), precipitation (PIG), and microbial reactions at surfaces (BIG). Some of the research activity from each IG is highlighted to the right. The IGs interact with each other as each interest group studies reactions across the molecular, microscopic, mesoscopic and, in most cases, field scales. For example, abiotic dissolution and precipitation reactions of Fe oxides as studied in the Dissolution IG provides the baseline for kinetic behavior as the BIG researches the interaction of microorganisms with these same minerals. The attachment of bacteria and redox chemistry that occurs between microorganisms and minerals are critical factors in maintaining groundwater quality and remediation of many toxic waste sites and is one of the main thrusts of research within our EMSI. The IGs also participate in using visualization tools to promote greater understanding of complex environmental data. As a whole, CEKA is also working to compile environmental kinetics data into a cyberinfrastructure and database. The database can be accessed at: http://keystone.ist.psu.edu/

Differential In Vitro Effects of Intravenous versus Oral Formulations of Silibinin on the HCV Life Cycle and Inflammation

Silymarin prevents liver disease in many experimental rodent models, and is the most popular botanical medicine consumed by patients with hepatitis C. Silibinin is a major component of silymarin, consisting of the flavonolignans silybin A and silybin B, which are insoluble in aqueous solution. A chemically modified and soluble version of silibinin, SIL, has been shown to potently reduce hepatitis C virus (HCV) RNA levels in vivo when administered intravenously. Silymarin and silibinin inhibit HCV infection in cell culture by targeting multiple steps in the virus lifecycle. We tested the hepatoprotective profiles of SIL and silibinin in assays that measure antiviral and anti-inflammatory functions. Both mixtures inhibited fusion of HCV pseudoparticles (HCVpp) with fluorescent liposomes in a dose-dependent fashion. SIL inhibited 5 clinical genotype 1b isolates of NS5B RNA dependent RNA polymerase (RdRp) activity better than silibinin, with IC50 values of 40–85 µM. The enhanced activity of SIL may have been in part due to inhibition of NS5B binding to RNA templates. However, inhibition of the RdRps by both mixtures plateaued at 43–73%, suggesting that the products are poor overall inhibitors of RdRp. Silibinin did not inhibit HCV replication in subgenomic genotype 1b or 2a replicon cell lines, but it did inhibit JFH-1 infection. In contrast, SIL inhibited 1b but not 2a subgenomic replicons and also inhibited JFH-1 infection. Both mixtures inhibited production of progeny virus particles. Silibinin but not SIL inhibited NF-κB- and IFN-B-dependent transcription in Huh7 cells. However, both mixtures inhibited T cell proliferation to similar degrees. These data underscore the differences and similarities between the intravenous and oral formulations of silibinin, which could influence the clinical effects of this mixture on patients with chronic liver diseases