scholarly journals Are multiple oxygen species selective in ethylene epoxidation on silver?

2018 ◽  
Vol 9 (4) ◽  
pp. 990-998 ◽  
Author(s):  
Emilia A. Carbonio ◽  
Tulio C. R. Rocha ◽  
Alexander Yu. Klyushin ◽  
Igor Píš ◽  
Elena Magnano ◽  
...  

We show atomic oxygen on an unreconstructed Ag(110) surface has a O 1s binding energy ≤ 528 eV and its stable at low coverages. Our findings point to the idea of multiple selective oxygen species in ethylene epoxidation on Ag.

2017 ◽  
Vol 121 (41) ◽  
pp. 22985-22994 ◽  
Author(s):  
Mustafa Karatok ◽  
Evgeny I. Vovk ◽  
Ali Vala Koc ◽  
Emrah Ozensoy

2003 ◽  
Vol 67 (23) ◽  
Author(s):  
V. I. Bukhtiyarov ◽  
M. Hävecker ◽  
V. V. Kaichev ◽  
A. Knop-Gericke ◽  
R. W. Mayer ◽  
...  

2015 ◽  
Vol 801 (2) ◽  
pp. 120 ◽  
Author(s):  
Jiao He ◽  
Jianming Shi ◽  
Tyler Hopkins ◽  
Gianfranco Vidali ◽  
Michael J. Kaufman

1992 ◽  
Vol 259 ◽  
Author(s):  
Satish Bedge ◽  
Joseph McFadyen ◽  
H. Henry Lamb

ABSTRACTRemoval of adsorbed organic contaminants from Si surfaces by reaction with molecular O3 and photo-generated atomic oxygen species in a UHV-compatible photochemical reactor was investigated. Treatment of contaminated wafers with externally generated O3 at 25°C was effective in removing adsorbed organics, but surface cleaning rates were enhanced by simultaneous 254-nm UV irradiation of the reactor contents. In situ photo-generation of O3 and atomic oxygen species by 185- and 254-nm irradiation of O2 gave comparable results. A simplified gas-phase kinetics model describing O3 generation by a low-pressure Hg lamp was developed and used to gain insight into the effects of relative humidity and O2 partial pressure on steady-state O3 concentrations.


1994 ◽  
Vol 9 (11) ◽  
pp. 2919-2924 ◽  
Author(s):  
Takeshi Tsuchida ◽  
Hideaki Takahashi

X-ray photoelectron spectra of hydrated aluminas (boehmite, diaspore, bayerite, and gibbsite), transition aluminas (y, δ, η, θ, X, and k –Al2O3) and corundum (α-Al2O3) have been studied for spectral characterization of each compound. The O1s spectra are shifted 0.2–1.2 eV to higher binding energy (Eb) in the order of α-Al2O3 < boehmite, diaspore < bayerite, gibbsite, and this agrees with the order of bulk OH/Al molar ratio in samples. The Eb and FWHM values of O1s spectra of transition aluminas depend on the ratio OH/O, i.e., the amount of OH− ions chemisorbed on them, and tend to decrease toward those of α-Al2O3 with increasing calcination temperature. Therefore, it is considered that an attracting effect of the proton on valence electrons in the hydroxyl oxygen causes the increased binding energy between core electrons and oxygen atomic nuclei. The broad O1s spectra of boehmite and diaspore can be deconvoluted into equal contribution from the two oxygen species in O2− and OH− ions in their structures.


2021 ◽  
Author(s):  
Kelath Murali Manoj ◽  
Abhinav Parashar ◽  
Vivian David Jacob ◽  
Daniel Andrew Gideon

Hemoglobin (Hb) transports oxygen via blood to various cells of the body and it is the most abundant protein found in erythrocytes. Herein, we propose an evidence-based hypothesis that Hb has a hitherto undiscovered function of serving as a murzyme (a redox enzyme working along the principles of murburn concept), catalyzing the synthesis of ATP in RBC, using diffusible reactive oxygen species (DROS). We support our hypothesis with theoretical arguments, earlier experimental findings and in silico explorations. The current work explains earlier reported in situ experimental findings/suggestions of 2,3-bisphosphoglycerate (BPG) and ADP binding at the same locus. We demonstrate that this interaction site is located at the heme cavity entrance with the binding energy in the order of BPG &gt; NADH &gt; ADP ~ ATP &gt; AMP, thereby explaining important physiological outcomes. The findings pose significant implications in routine physiology and pathologies like sickle cell anemia and thalassemia.


2019 ◽  
Vol 621 ◽  
pp. A75 ◽  
Author(s):  
Christian Eistrup ◽  
Catherine Walsh

Context. Detection of abundant O2 at 1–10% relative to H2O ice in the comae of comets 1P/Halley and 67P/Churyumov-Gerasimenko has motivated attempts to explain the origin of the high O2 ice abundance. Recent chemical modelling of the outer, colder regions of a protoplanetary disk midplane has shown production of O2 ice at the same abundance as that measured in the comet. Aims. We aim to carry out a thorough investigation to constrain the conditions under which O2 ice could have been produced through kinetic chemistry in the pre-solar nebula midplane. Methods. We have utilised an updated chemical kinetics code to evolve chemistry under pre-solar nebula midplane conditions. Four different chemical starting conditions and the effects of various chemical parameters have been tested. Results. Using the fiducial network, and for either reset conditions (atomic initial abundances) or atomic oxygen only conditions, the abundance level of O2 ice measured in the comets can be reproduced at an intermediate time, after 0.1–2 Myr of evolution, depending on ionisation level. When including O3 chemistry, the abundance of O2 ice is much lower than the cometary abundance (by several orders of magnitude). We find that H2O2 and O3 ices are abundantly produced (at around the level of O2 ice) in disagreement with their respective abundances or upper limits from observations of comet 67P. Upon closer investigation of the parameter space, and varying parameters for grain–surface chemistry, it is found that for temperatures 15–25 K, densities of 109−1010 cm−3, and a barrier for quantum tunnelling set to 2 Å, the measured level of O2 ice can be reproduced with the new chemical network, including an updated binding energy for atomic oxygen (1660 K). However, the abundances of H2O2 and O3 ices still disagree with the observations. A larger activation energy for the O + O2 → O3 reaction (Eact > 1000 K) helps to reproduce the non-detection of O3 ice in the comet, as well as reproducing the observed abundances of H2O2 and O2 ices. The only other case in which the O2 ice matches the observed abundance, and O3 and H2O2 ice are lower, is the case when starting with an appreciable amount of oxygen locked in O2. Conclusions. The parameter space investigation revealed a sweet spot for production of O2 ice at an abundance matching those in 67P and 1P, and O3 and H2O2 ice abundances matching those in 67P. This means that there is a radial region in the pre-solar nebula from 120–150 AU, within which O2 could have been produced in situ via ice chemistry on grain surfaces. However, it is apparent that there is a high degree of sensitivity of the chemistry to the assumed chemical parameters (e.g. binding energy, activation barrier width, and quantum tunnelling barrier). Hence, because the more likely scenario starting with a percentage of elemental oxygen locked in O2 also reproduces the O2 ice abundance in 67P at early stages, this supports previous suggestions that the cometary O2 ice could have a primordial origin.


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