scholarly journals Evaluation of usage-induced degradation of different endodontic file systems

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shekhar Bhatia ◽  
Venkatesh Nagendrababu ◽  
Ove A. Peters ◽  
Amr Fawzy ◽  
Umer Daood
Keyword(s):  
Photoelectron Spectroscopy ◽  
Surface Defects ◽  
File System ◽  
File Systems ◽  
Passive Layer ◽  
Binding Energies ◽  
X Ray Diffraction ◽  
X Ray ◽  
Before And After

AbstractTo evaluate structural profiles and mechanical behaviour of WaveOne Gold (WOG), Twisted File Adaptive (TFA) and XP-endo shaper (XPS) instruments after root canal preparation. Standardized in vitro shaping was performed in presence of 5.25% sodium hypochlorite. File morphology was analyzed using scanning electron microscopy; X-ray diffraction analysis was performed before and after use along with Raman spectroscopy. Nanoindentation was carried out to characterize surface topography. Ni2+ release was measured at 1, 3, 5 and 7 days. X-ray photoelectron spectroscopy (XPS) analysis was done before and after use. After allocating scan line shifts like in WOG, mechanical deformation was shown using first order polynomials. XPS file system showed minimal grooves on surface. SEM of WOG instrument showed scraping surface defects. Hardness varied from 8.11 ± 0.99 GPa in TFA system to 6.7 ± 1.27 GPa and 4.06 ± 4.1 GPa in XPS and WOG. Ni2+ concentration from WOG was 171.2 μg/L. Raman peak at 540–545 cm−1 is attributed to Cr2O3. High resolution of Ti 2p spectrum show distinctive peaks with binding energies dominating in WOG, XPS and TFA file system. XRD exhibited NiTi phases with diffraction peaks. WOG files showed more surface deterioration and less passive layer formation as compared to TFA and XPS systems.

Oxidation of Alloy-X in Subcritical, Transition, and Supercritical Water

CORROSION ◽  
10.5006/3881 ◽  
2021 ◽  
Author(s):  
Zachary Karmiol ◽  
Dev Chidambaram
Keyword(s):  
Supercritical Water ◽  
Photoelectron Spectroscopy ◽  
Focused Ion Beam ◽  
Elevated Temperatures ◽  
Subcritical Water ◽  
Ion Beam ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nickel Based Superalloy ◽  
Before And After

This work investigates the oxidation of a nickel based superalloy, namely Alloy X, in water at elevated temperatures: subcritical water at 261°C and 27 MPa, the transition between subcritical and supercritical water at 374°C and 27 MPa, and supercritical water at 380°C and 27 MPa for 100 hours. The morphology of the sample surfaces were studied using scanning electron microscopy coupled with focused ion beam milling, and the surface chemistry was investigated using X-ray diffraction, Raman spectroscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy before and after exposure studies. Surfaces of all samples were identified to comprise of a ferrite spinel containing aluminum.

Characterization of X-ray irradiated graphene oxide coatings using X-ray diffraction, X-ray photoelectron spectroscopy, and atomic force microscopy

2013 ◽  
Vol 28 (2) ◽  
pp. 68-71 ◽  
Author(s):  
Thomas N. Blanton ◽  
Debasis Majumdar
Keyword(s):  
Atomic Force Microscopy ◽  
Graphene Oxide ◽  
Photoelectron Spectroscopy ◽  
High Energy ◽  
X Ray Diffraction ◽  
Carbon Phase ◽  
X Ray ◽  
Force Microscopy ◽  
Atomic Force ◽  
Before And After

In an effort to study an alternative approach to make graphene from graphene oxide (GO), exposure of GO to high-energy X-ray radiation has been performed. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM) have been used to characterize GO before and after irradiation. Results indicate that GO exposed to high-energy radiation is converted to an amorphous carbon phase that is conductive.

A study of adsorption and absorption mechanisms of copper in palygorskite

Clay Minerals ◽  
2008 ◽  
Vol 43 (2) ◽  
pp. 195-203 ◽  
Author(s):  
Y. F. Cai ◽  
J. Y. Xue
Keyword(s):  
Photoelectron Spectroscopy ◽  
Esr Spectra ◽  
X Ray Diffraction ◽  
X Ray ◽  
Tetrahedral Sites ◽  
Octahedral Cation ◽  
Spin Resonance ◽  
Before And After ◽  
Cu Ions ◽  
Complex Ion

AbstractDesorption experiments performed on four Cu-adsorbed palygorskites suggest that the leached Cu2+ ion originates at the surface and/or net-like interstice of the palygorskite fibres. The leached fraction, calculated from the quantities of adsorbed Cu2+ before and after desorption, is <1%. This may indicate that the majority of Cu is in inaccessible structural sites. X-ray diffraction, X-ray photoelectron spectroscopy, Fourier transform infrared (FTIR) spectroscopy and electron spin resonance (ESR) were used to determine the mineralogical character of the Cu-adsorbed palygorskite. Two photoelectron lines at 932.5 and/or 933.7 eV in the narrow scan Cu 2p3/2 spectra show that Cu adsorbed on the surface of palygorskite is in the Cu+ and Cu2+ state. The stretching vibrations of the octahedral cation shift ~3–5 cm–1 towards a greater wavenumber in the FTIR spectra of Cu-adsorbed palygorskite. It can be deduced that the Cu2+ is trapped in the channel of the palygorskite structure. The ESR spectra of the palygorskite give g values of 2.34, 2.12, 2.08 and 2.05, suggesting that some Cu ions cannot be reached by H+. These results confirm that Cu is adsorbed by palygorskite via three possible mechanisms: (1) the Cu is adsorbed onto the surface or in a net-like interstice, and its oxidation states are +1 and +2; (2) Cu forms a complex ion – [Cu(H2O)4]2+ or [Cu(H2O)6]2+, and is trapped in the channel; or (3) Cu enters into the hexagonal channel of the tetrahedral sites or the unoccupied octahedral sites of palygorskite.

Growth of Calcium Phosphate on Poled Piezoelectric Poly-L-lactic Acid Membrane by a Biomimetic Method

2007 ◽  
Vol 330-332 ◽  
pp. 703-706
Author(s):  
Chun Peng Huang ◽  
Dong Hua Guan ◽  
Kun Tian ◽  
Xin Min Chen ◽  
Lin Niu ◽  
...  
Keyword(s):  
Calcium Phosphate ◽  
Electric Field ◽  
Photoelectron Spectroscopy ◽  
Charged Surface ◽  
X Ray ◽  
Charged Surfaces ◽  
Before And After ◽  
Dc Electric Field ◽  
Biomimetic Method

The bioactivity of poled piezoelectric PLLA membrane was investigated by studying the calcium phosphate formation in vitro using a biomimetic method. Samples (φ10mm) were poled under DC electric field of 8~l0kV/cm at 70°C for 30 min followed by cooling under the electric field. Surface chemistry of the samples before and after poling treatment was studied by X-ray photoelectron spectroscopy (XPS). Poled/unpoled samples were immersed in supersaturated calcification solution (SCS) for periods up to 24 h (36.5°C). The surface morphology and composition of the soaked samples were evaluated by using scanning electron microscope (SEM) and X-ray diffraction analysis (XRD). Poled samples showed two different charged surfaces, negatively-charged surface (N-PLLA) and positively-charged surface (P-PLLA). On the N-PLLA surfaces, SEM together with XRD showed a gradually formed calcium phosphate (Ca-P), while no obvious Ca-P on either P-PLLA or unpoled samples was observed. This study demonstrated that poled piezoelectric PLLA substrates induce substantially higher level of Ca-P formation than electrically neutral substrates and only N-PLLA, however, can improve Ca-P formation after immersion in SCS.

Preparation of the Nano-Hydroxyapatite/Chitosan/Konjac Glucomannan Composite as a Novel Degradable Drug Delivery System

2008 ◽  
Vol 569 ◽  
pp. 357-360
Author(s):  
Gang Zhou ◽  
Yu Bao Li ◽  
Soo Wohn Lee
Keyword(s):  
Drug Delivery ◽  
Drug Delivery System ◽  
Delivery System ◽  
Konjac Glucomannan ◽  
In Vitro Test ◽  
X Ray Diffraction ◽  
X Ray ◽  
Before And After ◽  
Vitro Test

Nano-hydroxyapatite (n-HA)/chitosan (CS)/konjac glucomannan (KGM) composite was prepared by integrating composition and molding. Then, X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used to analyze the physical, chemical and degradable properties of the composite before and after in simulated body fluid (SBF). Moreover, study in vitro test for drug delivery revealed that the amount of released pentoxifylline (1-[5-oxohexyl]-3,7-dimethylxanthine)(PTX) reached a plateau and equaled 80% of the drug loaded in an implant. The newly develop n-HA/CS/KGM composite may serve as a good degradable biomaterial for implantable drug delivery system (IDDS) in bone tissue engineering.

scholarly journals Sorption of Molybdates and Tungstates on Functionalized Montmorillonites: Structural and Textural Features

Materials ◽  
2019 ◽  
Vol 12 (14) ◽  
pp. 2253 ◽  
Author(s):  
Magdalena Tuchowska ◽  
Barbara Muir ◽  
Mariola Kowalik ◽  
Robert P. Socha ◽  
Tomasz Bajda
Keyword(s):  
Photoelectron Spectroscopy ◽  
Low Cost ◽  
Inorganic Compounds ◽  
Ammonium Bromide ◽  
Reaction Products ◽  
X Ray Diffraction ◽  
X Ray ◽  
Before And After ◽  
Mineral Sorbent ◽  
Dimethyl Ammonium

Montmorillonite—the most popular mineral of the smectite group—has been recognized as a low-cost, easily available mineral sorbent of heavy metals and other organic and inorganic compounds that pollute water. The aim of this work was to determine the sorption mechanism and to identify the reaction products formed on the surface of montmorillonite and organo-montmorillonite after sorption of molybdates (Mo(VI)) and tungstates (W(VI)). Montmorillonites are often modified to generate a negative charge on the surface. The main objective of the study was to investigate and compare the features of Na-montmorillonite (Na-M), montmorillonite modified with dodecyl trimethyl ammonium bromide (DDTMA-M), and montmorillonite modified with didodecyl dimethyl ammonium bromide (DDDDMA-M) before and after sorption experiments. The material obtained after sorption was studied by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The XRD pattern showed the presence of a new crystallic phase in the sample that was observed under an SEM as an accumulation of crystals. The FTIR spectra showed bands related to Mo–O and W–O vibration (840 and 940 cm−1, respectively). The obtained results suggest that molybdenum(VI) and tungsten(VI) ions sorb onto the organo-montmorillonite in the form of alkylammonium molybdates and tungstates.

scholarly journals Dehydrogenation/rehydrogenation mechanism in aluminum destabilized lithium borohydride

2009 ◽  
Vol 24 (8) ◽  
pp. 2720-2727 ◽  
Author(s):  
Xuebin Yu ◽  
Guanglin Xia ◽  
Zaiping Guo ◽  
Huakun Liu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Hydrogen Desorption ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Lithium Borohydride ◽  
Hydrogen Storage Properties ◽  
X Ray ◽  
Before And After ◽  
Storage Properties ◽  
Desorption Cycle

LiBH4/Al mixtures with various mol ratios were prepared by ball milling. The hydrogen storage properties of the mixtures were evaluated by differential scanning calorimetry/thermogravimetry analyses coupled with mass spectrometry measurements. The phase compositions and chemical state of elements for the LiBH4/Al mixtures before and after hydrogen desorption and absorption reactions were assessed via powder x-ray diffraction, infrared spectroscopy, and x-ray photoelectron spectroscopy. Dehydrogenation results revealed that LiBH4 could react with Al to form AlB2 and AlLi compounds with a two-step decomposition, resulting in improved dehydrogenation. The rehydrogenation experiments were investigated at 600 °C with various H2 pressure. It was found that intermediate hydride was formed firstly at a low H2 pressure of 30 atm, while LiBH4 could be reformed completely after increasing the pressure to 100 atm. Absorption/desorption cycle results showed that the dehydrogenation temperature increased and the hydrogen capacity degraded with the increase of cycle numbers.

scholarly journals Study of a Hydrogen Inhibition Method with Sodium Tungstate for Wet Aluminum Dust Removal Systems

Coatings ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 431
Author(s):  
Bohan Zhang ◽  
Kaili Xu ◽  
Xin Zheng ◽  
Xiwen Yao ◽  
Yantong Wang ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Sodium Tungstate ◽  
Dust Removal ◽  
Explosion Hazard ◽  
X Ray Diffraction ◽  
Aluminum Particles ◽  
X Ray ◽  
Before And After ◽  
Fire And Explosion ◽  
Hydrogen Inhibition

Hydrogen, which can be produced due to the accumulation of aluminum dust that reacts with water in wet dust removal systems, is a fire and explosion hazard. To reduce hydrogen production, sodium tungstate is used in hydrogen inhibition experiments to inhibit the reaction between aluminum dust and water. The purity of the aluminum powder was 95.15%, analyzed with X-ray fluorescence spectrometry (XRF). Each of the hydrogen inhibition experiments lasted for 12 h. In addition, scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) were used to characterize the surface morphology and composition of particles before and after the experiments. There was nearly no hydrogen produced when the concentration of the sodium tungstate solution reached 100 g/L. The results show that a protective coating containing W element was formed on the surface of the aluminum particles after the reaction with sodium tungstate, and the coating prevented the aluminum particles from contacting with water.

Controlled Crystallization of Tooth-Like Hydroxyapatite under Gelatin Monolayer

2007 ◽  
Vol 330-332 ◽  
pp. 663-666
Author(s):  
Kun Tian ◽  
Dong Hua Guan ◽  
Ping Wu ◽  
Chun Peng Huang ◽  
Lin Niu ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Molar Ratio ◽  
Dentinal Tubule ◽  
X Ray Diffraction ◽  
X Ray ◽  
Whole Process ◽  
Crosslinking Process ◽  
Recognition Theory ◽  
Parallel Direction

Based on the molecular recognition theory, an organic molecules model was designed to induce the hydroxyapatite crystallization, to build a tooth-like calcium phosphate/hydroxyapatite under a controllable way in vitro. The cross-linking of collagen on the dentin surface and gelatin was optimized by varying the molar ratio of N,N-(3-dimethylaminopropyl)- N'-ethyl-carbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS) at a constant EDC concentration. CaCl2 and Na3PO4-12H2O solutions were added after the crosslinking process. The whole process requires repeating the crosslinking and mineralization process for five times. The obtained composite were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) as well as energy dispersive X-ray photoelectron spectroscopy (XPS). The results showed that the dentinal tubule were blocked by neonatal hydroxyapatite layer which has a continuous structure of columns crystal with size of 10-40nm. Furthermore, there was column crystal with parallel direction inside, similar to the crystal array in the top of enamel rod. This study showed that the specific organic molecule model can be used as a potential effective crystal growth modifier.

scholarly journals In vitro bioactivity of glass-ceramic/fibroin composites

2017 ◽  
Vol 11 (2) ◽  
pp. 136-146 ◽  
Author(s):  
Lachezar Radev ◽  
Irena Michailova ◽  
Silviya Stateva ◽  
Diana Zaimova ◽  
Hristo Georgiev ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Inductively Coupled Plasma ◽  
Atomic Emission ◽  
Xrd Analysis ◽  
In Vitro Tests ◽  
In Vitro Bioactivity ◽  
X Ray ◽  
Before And After ◽  
Static Conditions

Bioactive composite materials were prepared by mixing 20 wt.% of silk fibroin (SF) and 80 wt.% of glassceramics from CaO-SiO2-P2O5-MgO system. In vitro bioactivity of the prepared composites was evaluated in 1.5 simulated body fluid (1.5 SBF) in static conditions. The obtained samples before and after in vitro tests were characterized by X-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The changes in 1.5 SBF solutions after soaking the samples were evaluated by inductively coupled plasma atomic emission spectroscopy (ICP-AES). MG63 osteosarcoma cells were used for the biological experiments. The obtained experimental data proved that the synthesized composites exhibit excellent in vitro bioactivity.

Sign in / Sign up

Export Citation Format

Share Document