2-Chloroaniline is widely used in polymer, rubber, pharmaceutical and dye industries[1].
Determination of 2-chloroaniline in polymer industrial wastewater has been examined using HPLC with on-line microdialysis[2].
Degradation of 2-chloroaniline in water by ozonation as well as by photolysis (UV-light of 254 nm) and radiolysis (γ-rays) in the presence of ozone has been investigated[3].
Journal of chromatography. A, 733(1-2), 19-34 (1996-05-10)
The environmental analysis of amines is important to preserve human health because these compounds often have toxic effects. Gas chromatography (GC) of free amines is generally unsatisfactory owing to the adsorption and decomposition of the solutes on the column. Derivatization
Journal of hazardous materials, 170(2-3), 1041-1049 (2009-06-16)
The aim of the present work is to investigate the effect of a prolonged leaching test (more than a year) on the microstructure of solidified cementitious wasteforms. A set of four different cement-based monoliths (Ap, Bp, Cp and Dp) was
Journal of hazardous materials, 157(2-3), 599-604 (2008-02-22)
Fuel oil fly ash has been tested as low-cost carbon-based adsorbent of 2-chlorophenol (CP), 2-chloroaniline (CA) and methylene blue (MB) from aqueous solutions. In all the cases the adsorption was found to be of cooperative type. Different adsorption capacities were
Journal of the American Chemical Society, 132(40), 14048-14051 (2010-09-23)
The Pd-catalyzed condensation of 2-bromostyrene and 2-chloroaniline derivatives yields stable diphenylamine intermediates, which are selectively converted to five-, six-, or seven-membered heteroaromatics (indoles, carbazoles, acridines, and dibenzazepines). The selectivity of these intramolecular transformations is uniquely ligand-controlled and offers efficient routes
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