ON THE ROLE OF PERHYDROXYL RADICAL AS AN OXIDIZING AGENT

Author(s):  
A. Nadezhdin ◽  
H.B. Dunford
RSC Advances ◽  
2015 ◽  
Vol 5 (4) ◽  
pp. 3104-3112 ◽  
Author(s):  
R. E. Rojas-Hernandez ◽  
M. A. Rodriguez ◽  
J. F. Fernandez

Well-controlled fuel/oxidizing agent ratio allows to synthesize nanostructured strontium aluminates lamellar particles with high luminescence properties.


2016 ◽  
Vol 69 (11) ◽  
pp. 1677-1682 ◽  
Author(s):  
Moonkyong Na ◽  
In Ho Kang ◽  
Jeong Hyun Moon ◽  
Wook Bahng
Keyword(s):  

1978 ◽  
Vol 133 (3) ◽  
pp. 1150-1155 ◽  
Author(s):  
K A Hibberd ◽  
P B Berget ◽  
H R Warner ◽  
J A Fuchs

1988 ◽  
Vol 135 (1) ◽  
pp. 301-315
Author(s):  
J. R. Bailey ◽  
W. R. Driedzic

Cardiac myoglobin plays a role in oxygen consumption and has a protective effect during periods of hypoxia, but little is known about the role of myoglobin during periods of ischaemia. Myoglobin-rich sea raven hearts and myoglobin-poor ocean pout hearts were isolated and perfused at varying flow rates and under conditions of low and high oxygen demand to assess the role of myoglobin in oxygen extraction. In the myoglobin-rich hearts, oxygen extraction remained constant over the flow range. In the myoglobin-poor hearts, oxygen extraction was significantly elevated, relative to controls, at the lower flow rates but decreased as the flow rate increased. In hearts where myoglobin was inactivated by an oxidizing agent, oxygen extraction was similar to that observed in myoglobin-poor hearts. Under conditions of high oxygen demand, myoglobin-rich hearts again showed a constant oxygen extraction over the flow range. Myoglobin-inactivated hearts had a significantly elevated oxygen extraction at low flows, and this decreased as flow rate increased. These data suggest that myoglobin renders oxygen extraction by fish hearts independent of the rate of perfusion.


2019 ◽  
Vol 8 (1) ◽  
pp. 288-296 ◽  
Author(s):  
Alif Duereh ◽  
Chokchai Boonchuay ◽  
Piyapong Buahom ◽  
Surat Areerat

Abstract Molecular weight reduction of natural rubber (NR) with hydrogen peroxide (H2O2) oxidizing agent is limited in biphasic water-toluene systems that is attributed to mass transfer. In this work, CO2 was applied to the (aqueous H2O2)-(toluene-NR) systems with the objective of improving reaction efficiency. Experiments were performed on the reaction system with CO2 at 12 MPa and at reaction temperatures and times of 60°C–80°C and 1 h–10 h to evaluate the reaction kinetics. CO2 could enhance the NR molecular weight reduction by lowering the activation energy (from 121 kJ·mol−1 to 38 kJ·mol−1). The role of CO2 in the reaction system seems to be the formation of oxidative peroxycarbonic acid intermediate and promotion of mass transport due to the reduction in the toluene-NR viscosity and interfacial tension. The epoxidized liquid NRs (M̅n=4.9×103 g·mol−1) obtained from NR molecular weight reduction was further processed to prepare hydroxyl telechelic NR (M̅n=1.0×103 g·mol−1) and biobased polyurethane.


1982 ◽  
Vol 34 (04) ◽  
pp. 937-946 ◽  
Author(s):  
Ronald H. Carson ◽  
Robert D. Norris ◽  
Richard Schellinger

Metals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 575
Author(s):  
Viet Nhan Hoa Nguyen ◽  
Si Jeong Song ◽  
Man Seung Lee

Platinum group metals (PGMs) are important for the manufacture of advanced materials in the field of catalysts and electronic devices. Since the chemical properties of PGMs are very similar to each other, hydrometallurgical processes should be employed to recover PGMs with high purity from either ores or secondary resources. In hydrometallurgical processes for PGMs, the first step is the dissolution of PGMs. For this purpose, inorganic acid solutions with oxidizing agents are generally employed. In this work, nonaqueous solvent leaching systems with a relatively cheap price were employed to investigate the dissolution of pure palladium (Pd) metal. The solvent leaching systems consisted of concentrated hydrochloric acid solution and commercial extractants such as tributyl phosphate (TBP), 7-hydroxydodecan-6-one oxime (LIX 63), and di-n-octyl sulfide (DOS) in the presence of H2O2 as an oxidizing agent. Among the three systems, TBP showed the best efficiency for the dissolution of Pd. The effect of several parameters like TBP concentration, temperature, time, stirring speed and the weight ratio of Pd to TBP/HCl/H2O2 was explored. The dissolution percentage of Pd by the HCl–H2O2–TBP system was higher than by the HCl–H2O–H2O2 system at the same concentration of HCl and H2O2. The role of TBP in enhancing the dissolution of Pd was discussed on the basis of the interaction between HCl and TBP. Compared to aqueous systems, mass transfer is important in the dissolution of Pd metal by the solvent leaching system. Optimum conditions for the complete dissolution of Pd were obtained.


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