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Nitrobenzene

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.


Papers
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Journal ArticleDOI
TL;DR: A more practical non-Pd cathodic electrocatalyst could be prepared and applied for electrocatalytic reduction of refractory pollutants in water and wastewater, and extend the promising applications of TiO2 in the fields of environmental science.
Abstract: TiO2 is a typical semiconductor and has been extensively used as an effective photocatalyst for environmental pollution control. But it could not be used as an electrochemical reductive catalyst because of its low electric conductivity and electrocatalytic activity. In this work, however, we demonstrate that TiO2 can act as an excellent cathodic electrocatalyst when its crystal shape, exposed facet and oxygen-stoichiometry are finely tailored by the local geometric and electronic structures. The defect-engineered TiO2–x single crystals dominantly exposed by high-energy {001} facets exhibits a high cathodic activity and great stability for electrochemical reduction of nitrobenzene, a typical refractory pollutant with high toxicity in environment. The single crystalline structure, the high-energy {001} facet and the defective oxygen vacancy of the defect-engineered TiO2–x single crystals are found to be mainly responsible for their cathodic superiority. With the findings in this work, a more practical non-P...

101 citations

Journal ArticleDOI
TL;DR: In this article, the authors used convolution analysis to evaluate the thermodynamic and kinetic parameters of two charge transfer systems at the water/nitrobenzene interface: Cs+ ion transfer and the electron transfer between ferrocene in nitrobenzinene and hexacyanoferrate(III) in water.

101 citations

Journal ArticleDOI
TL;DR: In this article, the first time 100% selectivity was established for the continuous gas phase hydrogenation of p-CNB to p-chloroaniline for reaction over a series of oxide and carbon supported Ni catalysts under mild reaction conditions.
Abstract: We have established for the first time 100% selectivity in the continuous gas phase hydrogenation of p-chloronitrobenzene (p-CNB) to p-chloroaniline for reaction over a series of oxide and carbon supported Ni catalysts (6 ± 2%, w/w) under mild reaction conditions (T = 393 K, P = 1 atm). Catalyst activation by temperature programmed reduction (TPR) is addressed, BET area and H2 uptake measurements provided and mean metal particle sizes evaluated by transmission electron micrographic (TEM) analysis. The following activity sequence has been determined: Ni/Al2O3 > Ni/SiO2 > Ni/Activated Carbon > Ni/graphite. Pd/Al2O3, as an alternative catalyst, delivered an appreciably higher activity but with the production of nitrobenzene (principal product) and aniline (secondary product), i.e. hydrodechlorination with subsequent –NO2 reduction prevailed. Exclusive formation of the corresponding haloaniline is also demonstrated for the hydrogenation of o-chloronitrobenzene, m-chloronitrobenzene and p-bromonitrobenzene over Ni/Al2O3. A lower hydrogenation rate is established for p-CNB relative to nitrobenzene, consistent with a halogen substituent deactivation effect. While the Ni catalysts suffered a loss of activity with time-on-stream, exclusive selectivity to the haloamine product was maintained. These preliminary results can serve as a basis for the development of a cleaner, high throughput production of commercially important haloamines.

101 citations

Journal ArticleDOI
TL;DR: In this article, surface and interfacial tension in systems formed by Brazilian crude oil n-pentane insolubles (C5I) and n-heptane (C7I) in the aromatic solvents toluene, pyridine, and nitrobenzene were measured at room temperature using the ring method and employing an automatic tensiometer.
Abstract: Data on the behavior of crude oil n-pentane- and n-heptane-insoluble fractions in aromatic solvent systems were obtained. Surface and interfacial tensions in systems formed by Brazilian crude oil n-pentane insolubles (C5I) and n-heptane insolubles (C7I) in the aromatic solvents toluene, pyridine, and nitrobenzene were measured at room temperature using the ring method and employing an automatic tensiometer. The results indicated possible asphaltene aggregation as well as the probable existence of critical micelle concentrations for both C5I and C7I fractions in each of the three solvents considered. Critical micelle concentrations measured for the C5I fraction in toluene and pyridine solutions were consistently higher than those in systems containing the C7I fraction, indicating a lower association tendency in the C5I fraction. Average molecular areas for asphaltenes adsorbed at different interfaces estimated from surface tension measurements were found to be in agreement with literature values and appear...

100 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023171
2022342
2021123
2020129
2019123
2018146