Analysis of CoCrMo Surface Oxide Removal by Alumina Blasting before Porcelain Firing in Dental Restorations

2012 ◽  
Vol 730-732 ◽  
pp. 9-14 ◽  
Author(s):  
Bruno Henriques ◽  
Filipe Silva ◽  
Delfim Soares
Keyword(s):  
Heat Treatment ◽  
Surface Roughness ◽  
Chemical Composition ◽  
High Alumina ◽  
X Ray ◽  
Dental Restorations ◽  
Ceramic Bond ◽  
Xrf Scanning ◽  
Oxide Removal

The purpose of this work was to perform a chemical and mechanical characterization of a preoxidized CoCrMo alumina blasted surface. This is a commonly performed surface treatment used in metal-porcelain systems for dental restorations to remove oxides formed during preoxidation heat treatment from the metal’s surface. CoCrMo dental alloy’s specimens produced by lost wax process were examined in terms of chemical composition using X-Ray fluorescence spectroscopy (XRF), Scanning Electron Microscopy (SEM) and Energy Dispersive X-Ray Spectroscopy (EDS); in terms of mechanical characteristics through the means of a microhardness test and in terms of surface roughness using a profilometer. It was investigated the chemical composition of various surface conditions: non-preoxidized, preoxidized, ground oxidized surface and sandblasted oxidized surface. After alumina blasting, the oxides level on metal’s surface remained high. Alumina blasting treatment (Ø110 µm) produced an 84% increase of CoCrMo surface hardening and an increase in surface roughness (Ra=0.58 µm). It was found alumina contaminants on the metal’s surface. Therefore, it was concluded that alumina blasting do not entirely removes the oxide layer formed during preoxidation heat treatment. It produced a chemical and mechanical surface modification that can influence the metal-ceramic bond strength.

scholarly journals Nanotechnology in Roman Opaque Red Glass from the 2nd Century AD. Archaeometric Investigation in Red Sectilia from the Decoration of the Lucius Verus Villa in Rome

Heritage ◽  
2019 ◽  
Vol 2 (3) ◽  
pp. 2597-2611 ◽  
Author(s):  
Mario Bandiera ◽  
Patrice Lehuédé ◽  
Marco Verità ◽  
Luis Alves ◽  
Isabelle Biron ◽  
...  
Keyword(s):  
Chemical Composition ◽  
Chemical Characterization ◽  
Second Step ◽  
Colorimetric Analysis ◽  
Historical Sources ◽  
Pixe Analysis ◽  
X Ray ◽  
Colorimetric Measurements ◽  
Shed Light

This work aims to characterise the chemical composition of Roman opaque red glass sectilia dated to the 2nd century A.D and to shed light on Roman glassmaking production of different shades of red, from red to reddish-brown. Due to the lack of technical historical sources for this period many questions about technological aspects still remain. In this project a multi-disciplinary approach is in progress to investigate the red glass sectilia with several red hues from the Imperial Villa of Lucius Verus (161–169 A.D.) in Rome. First, colorimetric measurements were taken to identify the various red hues. The second step was chemical characterization of the samples and the identification of crystalline colouring phases. Particle Induced X-Ray Emission (PIXE) analysis was used to investigate the chemical composition of these glass samples, while the crystalline phases were identified by Raman Spectroscopy and Scanning Electrons Microscope with Energy Dispersive X-ray Spectrometry (SEM-EDS). Using SEM-EDS nanoparticles were detected as a colouring agent, the chemical composition and the morphology of which has been studied in depth. This information has been compared with the colorimetric analysis to establish any correlation with the different colour hues.

scholarly journals Synthesis and characterization of apatite silicated powders with wet precipitation method

2021 ◽  
Vol 234 ◽  
pp. 00106
Author(s):  
Houda Labjar ◽  
Hassan Chaair
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Analytical Techniques ◽  
Precipitation Method ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wet Precipitation ◽  
Scanning Electron

The synthesis of apatite silicated Ca10(PO4)6-x(SiO4)x(OH)2-x (SiHA) with 0≤x≤2 was investigated using a wet precipitation method followed by heat treatment using calcium carbonate CaCO3 and phosphoric acid H3PO4 and silicon tetraacetate SiC8H20O4 (TEOS) in medium of water ethanol, with three different silicate concentrations. After drying, the samples are ground and then characterized by different analytical techniques like X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron Microscopy (SEM) and chemical analysis.

Characterization of Surface Roughness

2000 ◽  
Vol 6 (S2) ◽  
pp. 916-917
Author(s):  
John C. Russ
Keyword(s):  
Surface Roughness ◽  
Chemical Deposition ◽  
Irregular Surfaces ◽  
X Ray ◽  
Surface Areas ◽  
Raster Scan ◽  
Vertical Displacements ◽  
Physical And Chemical ◽  
Deposition Techniques

Because of the session at this Microscopy and Microanalysis 2000 meeting concerned with the microanalysis of irregular surfaces, it seems appropriate to briefly review the methods used for the characterization of rough surfaces. This includes both mathematical tools for the concise description of surface roughness, and instruments used to acquire the necessary data. These methods are widely used in industry to characterize and specify the roughness of surfaces prepared by various machining, grinding, polishing, chemical etching, and physical and chemical deposition techniques, and to correlate the surface roughness with performance.Historically, surface roughness has been measured by performing a linear traverse with a mechanical stylus that is sensitive to vertical displacements of nm but with a lateral resolution on the order of pm, which is quite similar to the dimensions of the region analyzed by X-ray microanalysis. Recently, more comprehensive characterizations have been obtained using a raster scan over surface areas.

Characterization of aluminosilicate (mullite) precursors prepared by a mechanochemical process

1998 ◽  
Vol 13 (8) ◽  
pp. 2184-2189 ◽  
Author(s):  
J. Temuujin ◽  
K. Okada ◽  
K. J. D. MacKenzie
Keyword(s):  
Heat Treatment ◽  
Nmr Spectra ◽  
Spinel Phase ◽  
Mas Nmr ◽  
X Ray Diffraction ◽  
Hydrated Alumina ◽  
X Ray ◽  
New Si ◽  
Grinding Time

Aluminosilicate precursors were prepared by mechanochemical treatment of gibbsitesilica gel mixtures. The effect of grinding on their structure and thermal behavior has been examined by 27Al and 29Si MAS NMR, x-ray diffraction (XRD), differential thermal analysis-thermogravimetry (DTA-TG), and Fourier transform infrared (FTIR). After 8 h grinding, the hydrated alumina was completely changed to an amorphous phase which showed a new exothermic DTA peak at about 980 °C due to the formation of γ–Al2O3 or spinel phase. This behavior was related to changes in the Al and Si environments, as deduced from the MAS NMR spectra. With increased grinding time, some 4-coordinated Al appears, together with an Al resonance at about 30 ppm. Simultaneously, a new Si resonance appears at about −90 ppm, indicating a greater degree of homogeneity in the ground samples. Mullite crystallizes at 1200 °C from samples ground for 8–20 h, its XRD intensity increasing with increased milling times, in agreement with the NMR, DTA, and FTIR data. Changes in the Al and Si environments during heat treatment, as reflected by the NMR spectra, are also reported.

Neodymium Incorporation in Zirconolite-Based Glass-Ceramics

2000 ◽  
Vol 663 ◽  
Author(s):  
P. Loiseau ◽  
D. Caurant ◽  
N. Baffier ◽  
C. Fillet
Keyword(s):  
Heat Treatment ◽  
Glass Ceramics ◽  
Fission Products ◽  
Treatment Temperature ◽  
Spent Fuel ◽  
X Ray Diffraction ◽  
Parent Glass ◽  
X Ray ◽  
Spin Resonance

ABSTRACTThe investigations on enhanced reprocessing of nuclear spent fuel, and notably on separating the long-lived minor actinides, such as Am and Cm, from the other fission products have led to the development of highly durable specific matrices such as glass-ceramics for their immobilization. This study deals with the characterization of zirconolite (CaZrTi2O7) based glass-ceramics synthesized by devitrification of an aluminosilicate parent glass. Trivalent actinide ions were simulated by neodymium, which is a paramagnetic local probe. Glass-ceramics with Nd2O3 contents ranging from 0 to 10 weight % were prepared by heat treatment of a parent glass at two different growth temperatures: 1050° and 1200°C. X-ray diffraction (XRD), energy dispersive X-ray analysis (EDX) and electron spin resonance (ESR) measurements clearly indicate that Nd3+ ions are partly incorporated in zirconolite crystals formed in the bulk of the glass-ceramic samples. The amount of neodymium in the crystalline phase was estimated using ESR results and was found to decrease with increasing either heat treatment temperature or total Nd2O3 content.

scholarly journals Effect of Liquid Ga on Metal Surfaces: Characterization of Morphology and Chemical Composition of Metals Heated in Liquid Ga

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Eun Je Lee ◽  
Min Goo Hur ◽  
Jeong Mun Son ◽  
Jeong Hoon Park ◽  
Seung Dae Yang
Keyword(s):  
Electron Microscope ◽  
Chemical Composition ◽  
Chemical Resistance ◽  
Maximum Amount ◽  
Liquid Gallium ◽  
Heating Process ◽  
X Ray ◽  
Metal Foils ◽  
Scanning Electron

This study investigates the effect of liquid gallium (Ga) on metal foils made of titanium (Ti), niobium (Nb), and molybdenum (Mo). The Ti, Nb, and Mo foils were heated in liquid Ga at 120°C for a maximum of two weeks. After heating, the changes in the morphology and the chemical composition of the metal foils were analyzed by using a field emission scanning electron microscope, energy-dispersive X-ray spectrometer, X-ray diffractometer, and X-ray photoelectron spectrometer. The results of the analysis indicated that the Nb foil showed the minimum adhesion of liquid Ga to the surface while the maximum amount of liquid Ga was observed to adhere to the Ti foil. In addition, the Nb foil was oxidized and the Mo foil was reduced during the heating process. Considering these effects, we conclude that Mo may be used as an alternative encapsulation material for Ga in addition to Nb, which is used as the conventional encapsulation material, due to its chemical resistance against oxidation in hot liquid Ga.

Influence of Heat Treatment on Structure and Properties of the Cast Magnesium Alloys

2006 ◽  
Vol 15-17 ◽  
pp. 491-496 ◽  
Author(s):  
Tomasz Tański ◽  
Leszek Adam Dobrzański ◽  
Lubomír Čížek
Keyword(s):  
Heat Treatment ◽  
Chemical Composition ◽  
Magnesium Alloys ◽  
Diffraction Method ◽  
Hardness Measurement ◽  
X Ray ◽  
Qualitative And Quantitative ◽  
Cast Alloys ◽  
Cast Magnesium Alloys ◽  
Cast Magnesium

In this paper is presented the structure and proprieties of the cast magnesium alloys as cast state and after heat treatment cooled with different cooling rate, depending on the cooling medium (furnace, water, air). For investigations samples in shape of 250x150x25 mm plates were used. The presented results concern X-ray qualitative and quantitative microanalysis as well as qualitative and quantitative X-ray diffraction method, tensile tests, hardness measurement. In the analysed alloys a structure of α %solid solution and fragile phase β (Mg17Al12) occurred mainly on grain borders as well as eutectic and phase AlMnFe, Mg2Si. Investigation are carried out for the reason of chemical composition influence and precipitation processes influence to the structure and mechanical properties of the magnesium cast alloys with different chemical composition in as cast alloys and after heat treatment.

scholarly journals CALCIUM OXIDE CHARACTERISTICS PREPARED FROM AMBUNTEN’S CALCINED LIMESTONE

2018 ◽  
Vol 5 (1) ◽  
pp. 65 ◽  
Author(s):  
Fatimatul Munawaroh ◽  
Laila Khamsatul Muharrami ◽  
Triwikantoro Triwikantoro ◽  
Zaenal Arifin
Keyword(s):  
Calcium Carbonate ◽  
Chemical Composition ◽  
Calcium Oxide ◽  
Crystalline Phase ◽  
Wave Number ◽  
Test Results ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxide Characteristics

<pre>Calcium oxide (CaO) and calcium carbonate (CaCO3) are widely used in industry. CaO and CaCO3 can be synthesized or derived from limestone. The purpose of this study to determine the characteristics of CaO calcined limestone from Ambunten Sumenep. Lime in calcined at 850 ° C for 6 hours. Characterization of X-ray fluorescence (XRF) was conducted to determine the chemical composition of limestone, X-ray diffraction test (XRD) to find the lime crystalline phase and FTIR test to determine the absorption of wave number. XRF test results showed that the limestone chemical composition consisted of Ca of 95.37% as the dominant element, Mg of 4.1%, Fe 0.17% and Y by 0.39%. The XRD test results showed that the limestone crystal phase is ankerite (Ca [Fe, Mg] [CO3] 2) and after the calcined phase calcination is vaterite (Ca [OH] 2), calcite (CaO) and calcite (CaCO3). While the FTIR test results show that the CaO spectra are seen at 3741.24, 1417.12 and 874.14 cm</pre><sup>-1</sup><pre>.</pre>

scholarly journals Elaboration and characterization of new phosphate glasses based on natural phosphate and red clay: influence of the chemical composition on the chemical durability

2019 ◽  
Vol 9 (3) ◽  
pp. 222-235 ◽  
Author(s):  
Oumaima Jamal Eddine ◽  
Mehdi El Bouchti ◽  
Omar Cherkaoui ◽  
Hassan Hannache ◽  
Said Gmouh
Keyword(s):  
Chemical Composition ◽  
Structural Investigation ◽  
Fluorescence Analysis ◽  
Chemical Durability ◽  
Phosphate Glasses ◽  
Red Clay ◽  
Natural Phosphate ◽  
X Ray ◽  
Quenching Method

New phosphate glass formulations based on Moroccan natural phosphate minerals alone or with Moroccan red clay additive (containing the P2O5-SiO2-CaO-Al2O3-MgO-Fe2O3-K2O-Na2O-TiO2 complex) have been successfully prepared by the quenching method. The chemical composition of each of the elaborated phosphate glasses was determined by X-ray fluorescence analysis (XRF). These investigated phosphate glasses have an excellent homogeneity as was verified by SEM. Their amorphous behavior was confirmed by XRD and DSC. The increase in density and glass transition temperature due to the addition of clay is believed to be related to the crosslinking of the phosphate chains. Structural investigation of these phosphate glasses was carried out using FTIR and Raman spectroscopies. The results obtained show that the composition of these glasses contains a mixture of ultraphosphate and polyphosphate structural units. The concentrations of this mixture depending on the initial composition of the glass components. A correlation between the chemical composition and the chemical durability of the investigated glasses was studied. The results showed that the dissolution rate of the glasses decreases by increasing the clay composition up to a point. This can be explained by assuming the formation of oxygen bridges and strong bonds within the various glasses.

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