Dissolution of UO2(s) in MgCl2-Brines Under Different Redox Conditions.

1992 ◽  
Vol 294 ◽  
Author(s):  
Ignasi Casas ◽  
J. Gimenez ◽  
J. De Pablo ◽  
M.E. Torrero

ABSTRACTThe dissolution of unirradiated UO2(s), with a particle size of 1 mm, has been studied in MgCl2 brines at 298 K under both reducing and oxidizing conditions. Results obtained under reducing conditions (H atmosphere in the presence of a palladium catalyst) show an initial increase of the total uranium concentration in solution and a subsequent decrease until equilibrium (or steady state) values are reached. Results obtained under oxidizing conditions (nominal oxygen partial pressures of 0.05, 0.21 and 1 atm) show two different trends. A relatively fast initial dissolution rate and, after approximately two or three weeks, a slower dissolution rate. X-Ray Photoelectron Spectroscopy (XPS) has shown that the UO2 surface composition changes during the experiment.

2005 ◽  
Vol 284-286 ◽  
pp. 453-456 ◽  
Author(s):  
Isabel B. Leonor ◽  
Hyun Min Kim ◽  
Francisco Balas ◽  
Kawashita Masakazu ◽  
Rui L. Reis ◽  
...  

A bioactive polyethylene polymer substrate can be produced by incorporation of sulfonic functional groups (-SO3H ) on its surface. Variation of the surface potential of the polyethylene modified with -SO3H groups with soaking in SBF were investigated using a laser electrophoresis zeta-potential analyzer. To complement the study using the laser electrophoresis, the surface was examined by X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy with an attached energy dispersive electron probe X-ray analyser (FE-SEM/EDS). It was found that the surface potential of the polyethylene was highly negative charged after soaking in SBF for 0.5 h, increased for higher soaking times (up to 48 h), and then decreased. The negative charge of the polymer at soaking time of 0.5 h is attributed to the presence of –SO3H groups on the surface. The initial increase in the surface potential was attributed to the incorporation of positively charged calcium ions to form a calcium sulphate, and then the subsequent decrease was assigned to the incorporation of negatively charged phosphate ions to form an amorphous calcium phosphate, which eventually transformed into apatite.


1973 ◽  
Vol 51 (10) ◽  
pp. 1670-1672 ◽  
Author(s):  
Norman Stewart McIntyre ◽  
Norman Henry Sagert ◽  
Rita Mary Louise Pouteau ◽  
Warren George Proctor

The surface composition of a series of nickel–chromia catalysts has been examined by X-ray photoelectron spectroscopy. Correlation of the amount of available surface nickel with the activity of the particular catalyst for hydrogen water deuterium isotope exchange is very good. No significant alterations are observed in the valence band spectra as the surface composition changes.


2011 ◽  
Vol 228-229 ◽  
pp. 130-134
Author(s):  
Jian Hua Yang ◽  
Song Li

Ti ions were implanted into H21 steel to improve the surface structure of oxides in H21 steel. The wear characteristics of the implanted steel was measured and compared to the performance of the un-implanted steel by a line-cutting apparatus and an optical interference microscope. The Ti concentration depth profile of the implanted steel was measured by Rutherford backscattering spectroscopy (RBS). The structure and composition of oxides were analyzed by X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD), respectively. The results showed that the improved wear resistance of the implanted steel was mainly due to the structure and composition changes of the surface oxides after Ti ion implantation.


2020 ◽  
Author(s):  
Jennifer A. Rudd ◽  
Ewa Kazimierska ◽  
Louise B. Hamdy ◽  
Odin Bain ◽  
Sunyhik Ahn ◽  
...  

The utilization of carbon dioxide is a major incentive for the growing field of carbon capture. Carbon dioxide could be an abundant building block to generate higher value products. Herein, we describe the use of porous copper electrodes to catalyze the reduction of carbon dioxide into higher value products such as ethylene, ethanol and, notably, propanol. For <i>n</i>-propanol production, faradaic efficiencies reach 4.93% at -0.83 V <i>vs</i> RHE, with a geometric partial current density of -1.85 mA/cm<sup>2</sup>. We have documented the performance of the catalyst in both pristine and urea-modified foams pre- and post-electrolysis. Before electrolysis, the copper electrode consisted of a mixture of cuboctahedra and dendrites. After 35-minute electrolysis, the cuboctahedra and dendrites have undergone structural rearrangement. Changes in the interaction of urea with the catalyst surface have also been observed. These transformations were characterized <i>ex-situ</i> using scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. We found that alterations in the morphology, crystallinity, and surface composition of the catalyst led to the deactivation of the copper foams.


2003 ◽  
Vol 18 (5) ◽  
pp. 1123-1130 ◽  
Author(s):  
V. Oliveira ◽  
R. Vilar

This paper aims to contribute to the understanding of column formation mechanisms in Al2O3–TiC ceramics micromachined using excimer lasers. Chemical and structural characterization of columns grown in Al2O3–TiC composite processed with 200 KrF laser pulses at 10 J/cm2 was carried out by scanning electron microscopy, transmission electron microscopy, x-ray photoelectron spectroscopy, and x-ray diffraction analysis. Fully developed columns consist of a core of unprocessed material surrounded by an outer layer of Al2TiO5, formed in oxidizing conditions, and an inner layer, formed in reducing conditions, composed of TiC and Al3Ti or an AlTi solid solution. Possible mechanisms of column formation are discussed.


Materials ◽  
2018 ◽  
Vol 11 (9) ◽  
pp. 1725 ◽  
Author(s):  
Xiaohong Liu ◽  
Ming Li ◽  
Xuemei Zheng ◽  
Elias Retulainen ◽  
Shiyu Fu

As a type of functional group, azo-derivatives are commonly used to synthesize responsive materials. Cellulose nanocrystals (CNCs), prepared by acid hydrolysis of cotton, were dewatered and reacted with 2-bromoisobuturyl bromide to form a macro-initiator, which grafted 6-[4-(4-methoxyphenyl-azo) phenoxy] hexyl methacrylate (MMAZO) via atom transfer radical polymerization. The successful grafting was supported by Fourier transform infrared spectroscopy (FT-IR) and Solid magnetic resonance carbon spectrum (MAS 13C-NMR). The morphology and surface composition of the poly{6-[4-(4-methoxyphenylazo) phenoxy] hexyl methacrylate} (PMMAZO)-grafted CNCs were confirmed with Transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The grafting rate on the macro-initiator of CNCs was over 870%, and the polydispersities of branched polymers were narrow. The crystal structure of CNCs did not change after grafting, as determined by X-ray diffraction (XRD). The polymer PMMAZO improved the thermal stability of cellulose nanocrystals, as shown by thermogravimetry analysis (TGA). Then the PMMAZO-grafted CNCs were mixed with polyurethane and casted to form a composite film. The film showed a significant light and pH response, which may be suitable for visual acid-alkali measurement and reversible optical storage.


2018 ◽  
Vol 122 (10) ◽  
pp. 2695-2702 ◽  
Author(s):  
E. Antonsson ◽  
C. Raschpichler ◽  
B. Langer ◽  
D. Marchenko ◽  
E. Rühl

2006 ◽  
Vol 600 (18) ◽  
pp. 3749-3752 ◽  
Author(s):  
C. Biswas ◽  
S. Banik ◽  
A.K. Shukla ◽  
R.S. Dhaka ◽  
V. Ganesan ◽  
...  

2014 ◽  
Vol 16 (39) ◽  
pp. 21486-21495 ◽  
Author(s):  
Josephina Werner ◽  
Jan Julin ◽  
Maryam Dalirian ◽  
Nønne L. Prisle ◽  
Gunnar Öhrwall ◽  
...  

The water–vapor interface of aqueous solutions of succinic acid, where pH values and bulk concentrations were varied, has been studied using surface sensitive X-ray photoelectron spectroscopy (XPS) and molecular dynamics (MD) simulations.


Author(s):  
Changqing Liu ◽  
David A. Hutt ◽  
Dezhi Li ◽  
Paul P. Conway

This paper aims to gain an insight into the correlation between the microstructure and surface composition of electroless Ni-P and its behaviour during soldering with Pb free alloys including Sn-3.8Ag-0.7Cu, Sn-3.5Ag and Sn-0.7Cu. Ni-P coatings with different P contents were produced through an industrial process on copper metal substrates. The surface morphology of these coatings was observed by Scanning Electron Microscopy (SEM) and the bulk composition was analyzed by means of Energy Dispersive X-ray analysis (EDX). The mechanical properties of the coatings were evaluated by nano-indentation testing under different maximum loads. However, to understand the behaviour of P in Ni-P coatings and deterioration of the coating surfaces during exposure to air, the surfaces of the coatings were also characterised by X-ray Photoelectron Spectroscopy (XPS) for storage at different temperatures. The dependence of the solderability of Ni-P coatings on the storage time and temperature was investigated by wetting balance testing, using an inactive or active flux with or without an inert N2 atmosphere. Finally, the solderability of Ni-P coatings to Pb free solders is correlated with their composition and microstructure (e.g. surface characteristics).


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