About: Nitrobenzene is a research topic. Over the lifetime, 5285 publications have been published within this topic receiving 83368 citations. The topic is also known as: essence of mirbane & nitrobenzol.
TL;DR: The properties of iron metal that make it useful in remediation of chlorinated solvents may also lead to reduction of other groundwater contaminants such as nitro aromatic compounds (NACs) as mentioned in this paper.
Abstract: The properties of iron metal that make it useful in remediation of chlorinated solvents may also lead to reduction of other groundwater contaminants such as nitro aromatic compounds (NACs). Nitrobenzene is reduced by iron under anaerobic conditions to aniline with nitrosobenzene as an intermediate product. Coupling products such as azobenzene and azoxybenzene were not detected. First-order reduction rates are similar for nitrobenzene and nitrosobenzene, but aniline appearance occurs more slowly (typical pseudo-first-order rate constants 3.5 × 10-2, 3.4 × 10-2, and 8.8 × 10-3 min-1, respectively, in the presence of 33 g/L acid-washed, 18−20 mesh Fluka iron turnings). The nitro reduction rate increased linearly with concentration of iron surface area, giving a specific reaction rate constant (3.9 ± 0.2 × 10-2 min-1 m-2 L). The minimal effects of solution pH or ring substitution on nitro reduction rates, and the linear correlation between nitrobenzene reduction rate constants and the square-root of mixing ra...
TL;DR: Fenton reagent has been used to test the degradation of different organic compounds in aqueous solution and eliminates the toxic substances and increases the biodegradability of the treated water (measured as the ratio BOD5/COD).
TL;DR: Carbon nanotubes (CNTs) have been found to activate persulfates (i.e., peroxymonosulfate and peroxydisulfate) into reactive species that are capable of oxidizing organic compounds in water.
TL;DR: The oxidation kinetics of butyl chloride, nitrobenzene, anisole, and methylmercury in the presence of hydroxyl radical (OH) scavengers were used to determine the rate and quantum efficiency for production of OH from irradiated nitrate ions in water.
Abstract: The oxidation kinetics of butyl chloride, nitrobenzene, anisole, and methylmercury in the presence of hydroxyl radical (OH) scavengers were used to determine the rate and quantum efficiency for production of OH from irradiated nitrate ions in water. The experiments were conducted under steady-state irradiations with monochromatic radiation (313 nm) and with sunlight. The mean quantum efficiency for OH production at 313 nm rises from 0.013 +/- 0.002 at 20 /sup 0/C to 0.017 +/- 0.003 at 30 /sup 0/C in the pH range 6.2-8.2. Results of this study are used to estimate nitrate-induced photooxidation rates of trace organic chemicals under a variety of environmental conditions. 27 references, 6 figures, 2 tables.
TL;DR: An indirect electrochemical method, which is very efficient for the degradation of organic pollutants in water, is described in this paper, which is based on electrocatalytical generation of Fenton's reagent to produce hydroxyl radicals, which are very active toward organic compounds.
Abstract: An indirect electrochemical method, which is very efficient for the degradation of organic pollutants in water, is described. The method, named electro-Fenton, is based on electrocatalytical generation of Fenton's reagent to produce hydroxyl radicals, which are very active toward organic compounds. An industrial pollutant, p-nitrophenol (PNP), was chosen for this study and was eventually mineralized. The major intermediary degradation products such as hydroquinone, benzoquinone, 4-nitrocatechol, 1,2,4-trihydroxybenzene and 3,4,5-trihydroxy- nitrobenzene were unequivocally identified by HPLC and GC-MS methods. The rate constants of the hydroxylation reactions were determined. The mineralization of the initial pollutant and the intermediates formed during electro-Fenton treatment was followed by total organic carbon (TOC) analyses. Dependence of mineralization on the amount of electrical energy consumed is shown by the relative decrease of TOC values. A mineralization reaction mechanism is proposed.