scholarly journals Homogeneous Incorporation of Gallium into Layered Double Hydroxide Lattice for Potential Radiodiagnostics: Proof-of-Concept

Nanomaterials ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 44
Author(s):  
Do-Gak Jeung ◽  
Tae-Hyun Kim ◽  
Jae-Min Oh
Keyword(s):  
Electron Microscopy ◽  
Layered Double Hydroxide ◽  
Inductively Coupled Plasma ◽  
Hydrothermal Reaction ◽  
Edge Structure ◽  
X Ray ◽  
Inductively Coupled ◽  
Diffraction Patterns ◽  
Double Hydroxide ◽  
X Ray Absorption

Trivalent gallium ion was successfully incorporated into chemically well-defined MgAl-layered double hydroxide (LDH) frameworks through postsynthetic hydrothermal treatment. Quantitative analysis with inductively coupled plasma-mass spectroscopy exhibited that Ga3+ was first incorporated into LDH through partial dissolution-precipitation at the edge of LDH particle and homogeneously distributed throughout the particle by substitution of Ga3+ for Al3+ in LDH frame works. The powder X-ray diffraction patterns showed that the Ga3+ incorporation did not affect the crystal structure without evolution of unexpected impurities. The morphology and surface property of LDH evaluated by scanning electron microscopy and light scattering showed the preservation of physicochemical properties throughout 24 h of hydrothermal reaction. The distribution of incorporated Ga3+ was visualized with energy dispersive spectroscopy-assisted transmission electron microscopy, suggesting the homogeneous location of Ga3+ in an LDH particle. The X-ray absorption near-edge structure and extended X-ray absorption fine structure suggested that the Ga moiety was immobilized in LDH from 0.5 h and readily crystallized upon reaction time.

Microstructure of TiC/Amorphous Hydrocarbon Nanocomposite Coatings

2000 ◽  
Vol 6 (S2) ◽  
pp. 440-441
Author(s):  
D. M. Cao ◽  
J. C. Jiang ◽  
B. Feng ◽  
W. J. Meng
Keyword(s):  
Inductively Coupled Plasma ◽  
High Hardness ◽  
Ceramic Surface ◽  
Edge Structure ◽  
X Ray ◽  
Inductively Coupled ◽  
Transmission Electron ◽  
Wide Range ◽  
Mechanical Components ◽  
X Ray Absorption

Application of an appropriate ceramic surface coating to mechanical components such as bearings and gears can provide longer life and increased performance reliability. Metal-containing hydrocarbon (Me-C:H) coatings possess high hardness, together with low friction and low wear rate. They have also been suggested to adhere better to metallic substrates. This combination of attractive mechanical/tribological properties makes Me-C:H coatings potentially useful for surface modification of a wide range of mechanical components.Using the technique of inductively coupled plasma (ICP) assisted vapor deposition[1], we have synthesized Ti-containing hydrocarbon (Ti-C:H) coatings with a wide range of Ti compositions[2]. Coating mechanical properties such as modulus and hardness have been measured by the technique of nanoindentation and correlated to Ti and hydrogen compositions[2,3].We have performed detailed microstructural examination of Ti-C:H coatings by transmission electron microscopy (TEM), Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy, and X-ray Absorption Near Edge Structure (XANES) spectroscopy.

scholarly journals Seleno-l-Methionine Is the Predominant Organic Form of Selenium in Cupriavidus metallidurans CH34 Exposed to Selenite or Selenate

2006 ◽  
Vol 72 (9) ◽  
pp. 6414-6416 ◽  
Author(s):  
Laure Avoscan ◽  
Richard Collins ◽  
Marie Carriere ◽  
Barbara Gouget ◽  
Jacques Cov�s
Keyword(s):  
Inductively Coupled Plasma ◽  
High Performance ◽  
Organic Form ◽  
Edge Structure ◽  
Cupriavidus Metallidurans Ch34 ◽  
X Ray ◽  
Inductively Coupled ◽  
Cupriavidus Metallidurans ◽  
Plasma Mass Spectrometry ◽  
X Ray Absorption

ABSTRACT The accumulated organic form of selenium previously detected by X-ray absorption near-edge structure (XANES) analyses in Cupriavidus metallidurans CH34 exposed to selenite or selenate was identified as seleno-l-methionine by coupling high-performance liquid chromatography to inductively coupled plasma-mass spectrometry.

scholarly journals Hydrothermal Synthesis of Ni/Al Layered Double Hydroxide Nanorods

2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Yun Zhao ◽  
Fenfei Xiao ◽  
Qingze Jiao
Keyword(s):  
Electron Microscopy ◽  
Reaction Time ◽  
Layered Double Hydroxide ◽  
Hydrothermal Reaction ◽  
Ph Value ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Double Hydroxide ◽  
Scanning Electron

Ni/Al layered double hydroxide (LDH) nanorods were successfully synthesized by the hydrothermal reaction. The crystal structure of the products was characterized by X-ray diffraction (XRD). The morphology of the products was observed using transmission electron microscopy (TEM) and field emission scanning electron microscopy (SEM). The influences of reaction time and pH value on the morphology of the Ni/Al LDHs were investigated. The result showed that the well-crystallized nanorods of Ni/Al LDHs could be obtained when the pH value was about 10.0 with a long reaction time (12–18 h) at 180°C.

scholarly journals An X-ray Absorption Near-Edge Structure (XANES) Study on the Oxidation State of Chromophores in Natural Kunzite Samples from Nuristan, Afghanistan

Minerals ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 463
Author(s):  
Habib Ur Rehman ◽  
Gerhard Martens ◽  
Ying Lai Tsai ◽  
Chawalit Chankhantha ◽  
Pinit Kidkhunthod ◽  
...  
Keyword(s):  
Oxidation State ◽  
Inductively Coupled Plasma ◽  
Oxidation States ◽  
Transition Elements ◽  
Edge Structure ◽  
X Ray ◽  
Inductively Coupled ◽  
Valence States ◽  
Icp Ms ◽  
X Ray Absorption

Kunzite, the pink variety of spodumene is famous and desirable among gemstone lovers. Due to its tenebrescent properties, kunzite always remains a hot research candidate among physicists and mineralogists. The present work is continuing the effort towards value addition to kunzite by enhancing its color using different treatments. Before color enhancement, it is essential to identify the chromophores and their oxidation states. In this paper, the authors investigated the main impurities in natural kunzite from the Nuristan area in Afghanistan and their valence states. Some impurities in the LiAlSi2O6 spodumene structure were identified and quantified by using sensitive techniques, including Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS), UV−VIS and X-ray absorption near-edge structure (XANES). LA-ICP-MS indicated many trace elements as impurities in kunzite, among which Fe and Mn are the main elements responsible for coloration. The oxidation states of these two transition elements were determined by the XANES technique. The study reveals that Mn is present in both Mn2+ and Mn3+ oxidation states, while Fe is present only in Fe3+ oxidation state.

scholarly journals Efflorescent Sulfate Crystallization on Fractured and Polished Colloform Pyrite Surfaces: A Migration Pathway of Trace Elements

Minerals ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 12
Author(s):  
Dimitrina Dimitrova ◽  
Vassilka Mladenova ◽  
Lutz Hecht
Keyword(s):  
Electron Microscopy ◽  
Trace Elements ◽  
Inductively Coupled Plasma ◽  
Microprobe Analysis ◽  
Electron Microprobe Analysis ◽  
X Ray ◽  
Inductively Coupled ◽  
Migration Pathway ◽  
Plasma Mass Spectrometry ◽  
Scanning Electron

The colloform pyrite variety incorporates many trace elements that are released in the environment during rapid oxidation. Colloform pyrite from the Chiprovtsi silver–lead deposit in Bulgaria and its oxidation efflorescent products were studied using X-ray diffractometry, scanning electron microscopy, electron microprobe analysis, and laser ablation inductively coupled plasma mass spectrometry. Pyrite is enriched with (in ppm): Co (0.1–964), Ni (1.8–3858), Cu (2.9–3188), Zn (3.1–77), Ag (1.2–1771), As (8179–52,787), Se (2.7–21.7), Sb (48–17792), Hg (4–2854), Tl (1.7–2336), Pb (13–7072), and Au (0.07–2.77). Gypsum, anhydrite, szomolnokite, halotrichite, römerite, copiapite, aluminocopiapite, magnesiocopiapite, coquimbite, aluminocoquimbite, voltaite, and ammoniomagnesiovoltaite were identified in the efflorescent sulfate assemblage. Sulfate minerals contain not only inherited elements from pyrite (Cr, Fe, Co, Ni, Cu, Zn, Ag, In, As, Sb, Hg, Tl, and Pb), but also newly introduced elements (Na, Mg, Al, Si, P, K, Ca, Sc, Ti, V, Mn, Ga, Rb, Sr, Y, Zr, Sn, Cs, Ba, REE, U, and Th). Voltaite group minerals, copiapite, magnesiocopiapite, and römerite incorporate most of the trace elements, especially the most hazardous As, Sb, Hg, and Tl. Colloform pyrite occurrence in the Chiprovtsi deposit is limited. Its association with marbles would further restrict the oxidation and release of hazardous elements into the environment.

Photocatalytic Oxidation of Alcohols Over Magnetically Recoverable Gold Supported Iron Oxide Nanoparticles

2019 ◽  
Vol 11 (12) ◽  
pp. 1731-1738 ◽  
Author(s):  
Ma Hui ◽  
Wu Juzhen ◽  
Zhao Li ◽  
Zhou Zheng ◽  
Guo Jiahu
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Inductively Coupled Plasma ◽  
Photocatalytic Oxidation ◽  
Organic Dyes ◽  
Atomic Emission ◽  
One Pot ◽  
X Ray ◽  
Inductively Coupled ◽  
Oxidation Of Alcohols

A one-pot simple and efficient synthetic route for the synthesis of Au-loaded Fe2O3 nanoparticles was developed, and this material's photocatalytic activity for visible light assisted oxidation of alcohols and degradation of organic dye were studied. As-synthesized nanostructured catalyst was characterised by powder X-ray diffraction (XRD), transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), SEM-mapping, X-ray photoelectron spectroscopy (XPS), N2 adsorption–desorption isotherm (BET), and inductively coupled plasma-atomic emission spectroscopy (ICP-AES). It was observed that 5–10 nm Au-nanoparticles supported on 10–80 nm Fe2O3 shows boomerang-shaped nanoparticle. Gold loading of 1 wt% shows high conversion and selectivity towards the target product aldehyde. The synthesized nanomaterial also proved to be an excellent photocatalyst for degradation of organic dyes such as methylene blue (MB) and rhodamine B (RhB). The catalyst proved to be noteworthy as it does not loss in its catalytic activity even after five cycles of reuse.

Eyeing the past: synchrotron µ-XANES and XRF imaging of tarnish distribution on 19th century daguerreotypes

2019 ◽  
Vol 26 (5) ◽  
pp. 1679-1686 ◽  
Author(s):  
M. S. Kozachuk ◽  
T. K. Sham ◽  
R. R. Martin ◽  
A. J. Nelson ◽  
I. Coulthard
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Synchrotron Radiation ◽  
National Gallery ◽  
Edge Structure ◽  
X Ray ◽  
The Past ◽  
National Gallery Of Canada ◽  
X Ray Absorption ◽  
Scanning Electron

Louis-Jacques-Mandé Daguerre introduced the first successful photographic process, the daguerreotype, in 1839. Tarnished regions on daguerreotypes supplied by the National Gallery of Canada were examined using scanning electron microscopy energy-dispersive X-ray spectroscopy and synchrotron-radiation analysis. Synchrotron X-ray fluorescence imaging visualized the distribution of sulfur and chlorine, two primary tarnish contributors, and showed that they were associated with the distribution of image particles on the surface. X-ray absorption near-edge structure spectroscopy determined the tarnish to be primarily composed of AgCl and Ag2S. Au2S, Au2SO4, HAuCl4 and HgSO4 were also observed to be minor contributors. Environmental contamination may be a source of these degradation compounds. Implications of these findings will be discussed.

scholarly journals Acetalization of Glycerol with Citral over Heteropolyacids Immobilized on KIT-6

Catalysts ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 81
Author(s):  
José Castanheiro
Keyword(s):  
Electron Microscopy ◽  
Inductively Coupled Plasma ◽  
Fixed Time ◽  
Tungstophosphoric Acid ◽  
X Ray Diffraction ◽  
Glycerol Conversion ◽  
X Ray ◽  
Inductively Coupled ◽  
Catalytic Stability ◽  
Scanning Electron

Glycerol acetalization with citral was studied using a heteropolyacid (tungstophosphoric acid) supported on KIT-6, as a catalyst, at 100 °C. Different catalysts were synthesized. Catalysts were characterized by scanning electron microscopy (SEM), inductively coupled plasma (ICP), X-ray diffraction (XRD), attenuated total refletion-Fourier transform infrared spectroscopy (ATR-FTIR), and potentiometric titrations. At a fixed time, the glycerol conversion increased with the H3PW12O40 (PW) on KIT-6. PW4-KIT-6 material had a higher conversion than other catalysts. The optimization of glycerol’s acetalization with citral was studied under the PW4-KIT-6 catalyst. After 5 h, it was found that, at T = 100 °C, with m = 0.3 g of solid, molar glycerol:citral = 1:2.25, the conversion of glycerol was 89%. Moreover, the PW4-KTI-6 catalyst showed good catalytic stability.

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