Localisation of electrochemical oxidation processes in nickel and cobalt hexacyanoferrates investigated by analysis of the multiplet patterns in X-ray photoelectron spectra

2001 ◽  
Vol 3 (4) ◽  
pp. 562-569 ◽  
Author(s):  
Stefan Sauter ◽  
Gunther Wittstock ◽  
Rüdiger Szargan
Keyword(s):  
Electrochemical Oxidation ◽  
Photoelectron Spectra ◽  
X Ray ◽  
Oxidation Processes ◽  
Cobalt Hexacyanoferrates

scholarly journals Enhancement of the Activity of Electrochemical Oxidation of BPS by Nd-Doped PbO2 Electrodes: Performance and Mechanism

Water ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1317
Author(s):  
Yan Zhang ◽  
Zhili Ni ◽  
Jie Yao
Keyword(s):  
Energy Consumption ◽  
Electrochemical Oxidation ◽  
Energy Dispersive Spectrometer ◽  
X Ray Diffraction ◽  
Bisphenol S ◽  
X Ray ◽  
Oxidation Processes ◽  
Duty Cycles ◽  
Pbo2 Electrode ◽  
Pbo2 Electrodes

The electrochemical oxidation processes have attracted tremendous attention on the destruction of toxic and non-biodegradable organics. A series of neodymium (Nd)-doped PbO2 electrodes (Ti/PbO2-Nd) were synthesized through a pulse electrodeposition method, and its activity of bisphenol S (BPS) removal was further examined. The morphologies and structures were characterized by the X-ray diffraction (XRD), scanning electron microscopy (SEM) and an energy dispersive spectrometer (EDS). The performance, energy consumption and mechanism of electrochemical oxidation of BPS by Ti/PbO2-Nd electrode were also discussed. Compared to the traditional Ti/PbO2 electrode, the Ti/PbO2-Nd enables finer crystal particles, facilitating the oxygen evolution overpotential (OEP) from 1.41V to 1.55V and the generation of hydroxyl radicals (•OH). Moreover, lower duty cycles during the preparation of the electrode also contribute to the tapering size of crystals. The results show that the Ti/PbO2-Nd electrode exhibits relatively high activity in the anodic oxidation of BPS. Over 95% of BPS could be removed with the current density of 15 mA cm−2. Moreover, the energy consumption of BPS degradation on Ti/PbO2-Nd electrode is 60.26 kWh m−3, much lower than that on Ti/PbO2 electrode (95.45 kWh m−3). To conclude, the Ti/PbO2-Nd electrode has been proven to be a promising material for BPS removal.

scholarly journals Modification of Wood with Monoethanolamino-borate by The Data of X-Ray Photoelectron Spectroscopy

2018 ◽  
Vol 196 ◽  
pp. 04005
Author(s):  
Irina Stepina ◽  
Irina Kotlyarova
Keyword(s):  
Particle Size ◽  
Photoelectron Spectroscopy ◽  
Model Compound ◽  
Hydrolytic Stability ◽  
Photoelectron Spectra ◽  
Wood Cellulose ◽  
Rapid Loss ◽  
X Ray ◽  
Wood Protection ◽  
Cellulose Materials

The difficulty of wood protection from biocorrosion and fire is due to the fact that modifiers in use are washed out from the surface of the substrate under the influence of environmental factors. This results in a rapid loss of the protective effect and other practically important wood characteristics caused by the modification. To solve this problem is the aim of our work. Here, monoethanolaminoborate is used as a modifier, where electron-donating nitrogen atom provides a coordination number equal to four to a boron atom, which determines the hydrolytic stability of the compounds formed. Alpha-cellulose ground mechanically to a particle size of 1 mm at most was used as a model compound for the modification. X-ray photoelectron spectra were recorded on the XSAM-800 spectrometer (Kratos, UK). Prolonged extraction of the modified samples preceded the registration of the photoelectron spectra to exclude the fixation of the modifier molecules unreacted with cellulose. As a result of the experiment, boron and nitrogen atoms were found in the modified substrate, which indicated the hydrolytic stability of the bonds formed between the modifier molecules and the substrate. Therefore monoethanolaminoborate can be considered as a non-extractable modifier for wood-cellulose materials.

scholarly journals Impact of high temperatures on aluminoceladonite studied by Mössbauer, Raman, X-ray diffraction and X-ray photoelectron spectroscopy

2021 ◽  
Author(s):  
Mariola Kądziołka-Gaweł ◽  
Maria Czaja ◽  
Mateusz Dulski ◽  
Tomasz Krzykawski ◽  
Magdalena Szubka
Keyword(s):  
Photoelectron Spectroscopy ◽  
Integral Intensity ◽  
Photoelectron Spectra ◽  
X Ray Diffraction ◽  
Structural Reorganization ◽  
Oh Groups ◽  
X Ray ◽  
Al Content ◽  
Integral Intensity Ratio ◽  
Higher Temperature

AbstractMössbauer, Raman, X-ray diffraction and X-ray photoelectron spectroscopies were used to examine the effects of temperature on the structure of two aluminoceladonite samples. The process of oxidation of Fe2+ to Fe3+ ions started at about 350 °C for the sample richer in Al and at 300 °C for the sample somewhat lower Al-content. Mössbauer results show that this process may be associated with dehydroxylation or even initiate it. The first stage of dehydroxylation takes place at a temperature > 350 °C when the adjacent OH groups are replaced with a single residual oxygen atom. Up to ~500 °C, Fe ions do not migrate from cis-octahedra to trans-octahedra sites, but the coordination number of polyhedra changes from six to five. This temperature can be treated as the second stage of dehydroxylation. The temperature dependence on the integral intensity ratio between bands centered at ~590 and 705 cm−1 (I590/I705) clearly reflects the temperature at which six-coordinated polyhedra are transformed into five-coordinated polyhedra. X-ray photoelectron spectra obtained in the region of the Si2p, Al2p, Fe2p, K2p and O1s core levels, highlighted a route to identify the position of Si, Al, K and Fe cations in a structure of layered silicates with temperature. All the measurements show that the sample with a higher aluminum content and a lower iron content in octahedral sites starts to undergo a structural reorganization at a relatively higher temperature than the less aluminum-rich sample does. This suggests that iron may perform an important role in the initiation of the dehydroxylation of aluminoceladonites.

X-RAY PHOTOELECTRON SPECTRA OF PHOSPHORUS YLIDES. PROBING THE PHOSPHORUS-CARBON YLIDE BOND

1974 ◽  
Vol 3 (5) ◽  
pp. 405-408 ◽  
Author(s):  
Manabu Seno ◽  
Shinji Tsuchiya ◽  
Teruzo Asahara
Keyword(s):  
Photoelectron Spectra ◽  
Phosphorus Ylides ◽  
X Ray

scholarly journals Chemisorbed Oxygen or Surface Oxides Steer the Selectivity in Pd Electrocatalytic Propene Oxidation Observed by Operando Pd Ledge X‐ray Absorption Spectroscopy

2021 ◽  
Author(s):  
Sergey Koroidov ◽  
Anna Winiwarter ◽  
Oscar Alfonso Diaz-Morales ◽  
Mikaela Gorlin ◽  
Joakim Halldin Stenlid ◽  
...  
Keyword(s):  
Electrochemical Oxidation ◽  
Absorption Spectroscopy ◽  
Propene Oxidation ◽  
X Ray ◽  
Chemisorbed Oxygen ◽  
Oxidation Of Hydrocarbons ◽  
Surface Oxides ◽  
X Ray Absorption

Controlled electrochemical oxidation of hydrocarbons to desired products is an attractive approach in catalysis. Here we study the electrochemical propene oxidation under operando conditions using Pd L‐edge X‐ray absorption spectroscopy...

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