“…According to Tale et al . , the reaction of CAN with HCl generates in situ molecular chlorine, causing oxidative conversion of iodoarenes to (dichloroiodo) arenes. Similarly, Hwu and King concluded that CAN is responsible for enhanced destruction of other functional groups in the presence of acids like hydrogen chloride, hydrogen bromide, acetic acid, etc.…”
Oxidative degradation of azo chromophore based C. I. Reactive Blue 171 dye having recalcitrant triazine and naphthalene rings in the structure was attempted using ceric ammonium nitrate (CAN) as an oxidant. The extent of decolorization was evaluated, which was found to be maximum (93.1%) at pH 6.5 and CAN dosage 0.19 mM for 50 mg/L dye solution in 1 h. The COD removal was 30.9%. The kinetic study of dye degradation exhibited pseudo-firstorder kinetics. The effect of temperature was described by the Arrhenius equation and the activation energy was found to be 33.8 kJ/mol. The intermediates formed by the CAN treatment were analyzed by TLC, FTIR and HPLC, which indicated the breaking of bonds of the dye. GC/MS analysis indicated formation of smaller sulfonate fragments by azo bond cleavage. The degradation pathway for the dye pollutant has been predicted based on the characterization of the degradation products formed. Phytotoxicity, as analyzed by ANOVA, indicated results comparable with distilled water, revealing extensive reduction in toxicity of the dye upon CAN treatment. Thus, oxidative treatment with CAN gives effective decolorization, partial mineralization and extensive reduction in the toxicity of the dye RB 171, which allows safe reuse of the treated dye solution for irrigation purpose.
“…According to Tale et al . , the reaction of CAN with HCl generates in situ molecular chlorine, causing oxidative conversion of iodoarenes to (dichloroiodo) arenes. Similarly, Hwu and King concluded that CAN is responsible for enhanced destruction of other functional groups in the presence of acids like hydrogen chloride, hydrogen bromide, acetic acid, etc.…”
Oxidative degradation of azo chromophore based C. I. Reactive Blue 171 dye having recalcitrant triazine and naphthalene rings in the structure was attempted using ceric ammonium nitrate (CAN) as an oxidant. The extent of decolorization was evaluated, which was found to be maximum (93.1%) at pH 6.5 and CAN dosage 0.19 mM for 50 mg/L dye solution in 1 h. The COD removal was 30.9%. The kinetic study of dye degradation exhibited pseudo-firstorder kinetics. The effect of temperature was described by the Arrhenius equation and the activation energy was found to be 33.8 kJ/mol. The intermediates formed by the CAN treatment were analyzed by TLC, FTIR and HPLC, which indicated the breaking of bonds of the dye. GC/MS analysis indicated formation of smaller sulfonate fragments by azo bond cleavage. The degradation pathway for the dye pollutant has been predicted based on the characterization of the degradation products formed. Phytotoxicity, as analyzed by ANOVA, indicated results comparable with distilled water, revealing extensive reduction in toxicity of the dye upon CAN treatment. Thus, oxidative treatment with CAN gives effective decolorization, partial mineralization and extensive reduction in the toxicity of the dye RB 171, which allows safe reuse of the treated dye solution for irrigation purpose.
“…[309][310][311] For instance, the reaction of 1 with CAN and cyclodienes in acetonitrile resulted in the formation of 1,4-and 1,2-furonaphthoquinones (151)(152)(153)(154), as presented in Scheme 41. CAN, a well know one-electron oxidant, 307,308 easily handled and soluble in various solvents, is very useful in many reactions.…”
Section: Synthesis Of Other Heterocycles From Lawsone (1)mentioning
confidence: 99%
“…CAN, a well know one-electron oxidant, 307,308 easily handled and soluble in various solvents, is very useful in many reactions. [309][310][311] For instance, the reaction of 1 with CAN and cyclodienes in acetonitrile resulted in the formation of 1,4-and 1,2-furonaphthoquinones (151)(152)(153)(154), as presented in Scheme 41. 312 Additionally, manganese(III) acetate dihydrate can promote the radical cyclization of 1 with alkenes, leading selectively to 1,4-furonaphthoquinones (155a-d) in excellent yields (Scheme 41).…”
Section: Synthesis Of Other Heterocycles From Lawsone (1)mentioning
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.