EXPERIMENTAL
1, 10-phenanthroline (AR, Merck), propanol (AR, Qualigens), K2Cr2O7 (AR, BDH), sodium dodecyl sulphate (SDS) (AR, SRL), TX-100 (AR, SRL) and all other chemicals used were of highest degree of purity available commercially. All the solutions were prepared in double distilled water. Solutions of the oxidant and reaction mixtures containing the known quantities of the substrate(s) (i.e. propanol), promoter (1,10-phenanthroline) under the kinetic conditions [propanol]T>>[Cr(VI)]T acid and other necessary chemicals were separately thermostated (±0 ℃). The reaction was initiated by the requisite amounts of the oxidant with the reaction mixture. Progress of the reaction is monitored by following the rate of disappearance of Cr(VI). The concentration of Cr(VI) at different time intervals was measured by a titrimetric quenching technique using excess of standard Mohr’s solution and unreacted Fe(II) was estimated by a standard Ce(IV) solution using ferroin indicator.10a The pseudo first order rate constants were calculated from the slopes of the plot of log [Cr(VI)]t versus time t, which were linear at least for three half lives. The scanned spectra, spectrum after completion of the reaction and other spectra were recorded with a UV-VIS spectrophotometer [UV-1800 and UV-VIS NIR-3600 (SHIMADZU)]. Quartz cuvettes of path length 1 cm were used. Under the experimental conditions, the possibility of decomposition of the surfactants by Cr(VI) was investigated and the rate of decomposition in this path was kinetically negligible.
References
- Pawar, B.; Padalkar,V; Phatangare, K.; Nirmalkar, S.; Chaskar, A. Catal. Sci. Technol. 2011, 1, 1641. https://doi.org/10.1039/c1cy00278c
- Minkler, S. R. K.; Lipshutz, B. H.; Krause, N. Angew. Chem. 2011, 123, 7966. https://doi.org/10.1002/ange.201101396
- Dwars, T.; Paetzold, E.; Oehme, G. Angew. Chem. 2005, 117, 7338. https://doi.org/10.1002/ange.200501365
- Nishikata, T.; Lipshutz, B. H. Chem. Commun. 2009, 6472.
- Saha, R.; Ghosh, A.; Saha, B. J. Coord. Chem. 2011, 64, 3729. https://doi.org/10.1080/00958972.2011.630463
- Milano-Brusco, J. S.; Nowothnick, H.; Schwarze, M.; Schomacker, R. Ind. Eng. Chem. Res. 2010, 49, 1098. https://doi.org/10.1021/ie900753t
- Schwuger, M. J.; Stickdorn, K.; Schomacker, R. Chem. Rev. 1995, 95, 849. https://doi.org/10.1021/cr00036a003
- M. Gratzel, K. Kalyanasundaram, Eds. Kinetics and Catalysis in Microheterogeneous Systems; Marcel Dekker: New York, 1991.
- Sudaram, S.; Raghavan, P. S. Chromium-VI reagents: Synthetic Application; Springer: 2011.
- Saha, R.; Nandi, R.; Saha, B. J. Coord. Chem. 2011, 64, 1782. https://doi.org/10.1080/00958972.2011.583646
- Saha, B.; Orvig, C. Coord. Chem. Rev. 2010, 254, 2959. https://doi.org/10.1016/j.ccr.2010.06.005
- Meenakshisundaram, S. P.; Gopalkrishnan, M.; Nagarjan, S.; Sarathi, N. Catal. Commun. 2007, 8, 713. https://doi.org/10.1016/j.catcom.2006.08.033
- Madal, J; Chowdhury, K. M.; Paul, K.; Saha, B. J. Coord. Chem. 2010, 63, 99. https://doi.org/10.1080/00958970903302723
- Chowdhury, K. M.; Madal, J; Saha, B. J. Coord. Chem. 2009, 62, 1871. https://doi.org/10.1080/00958970802687547
- Islam, M.; Saha, B.; Das, A.K. J. Mol. Catal A: Chem. 2007, 266, 21 https://doi.org/10.1016/j.molcata.2006.10.042
- Islam, M.; Saha, B.; Das, A.K. J. Mol. Catal. A: Chem. 2005, 236, 260. https://doi.org/10.1016/j.molcata.2005.04.019
- Bayen, R.; Islam, M.; Saha, B.; Das, A. K. Carbohydr. Res. 2005, 340, 2163. https://doi.org/10.1016/j.carres.2005.07.002
- Meenakshisundaram, S.; Sarathi, N. Trans. Met. Chem. 2006, 31, 369.
- Meenakshisundaram, S.; Markkandan, R. Trans. Met. Chem. 2004, 29, 308. https://doi.org/10.1023/B:TMCH.0000020374.24384.38
- Khan, Z.; Masan, S.; Ud-Din, Raju, Kabir. Trans. Met. Chem. 2003, 28, 881. https://doi.org/10.1023/A:1026303415289
- Ghosh, S. K.; Basu, A.; Saha, R.; Ghosh, A.; Mukherjee, K.; Saha, B. J. Coord. Chem. (Revised Manuscript has been sent for consideration).
- Madal, J.; Chowdhury, K. M.; Paul, K. K.; Saha, B. Open Catal. J. 2008, 1, 1. https://doi.org/10.2174/1876214X00801010001
Cited by
- Hetero-aromatic Nitrogen Base Promoted Cr(VI) Oxidation of Butanal in Aqueous Micellar Medium at Room Temperature and Atmospheric Pressure vol.45, pp.1, 2016, https://doi.org/10.1007/s10953-016-0434-5
- Suitable combination of promoter and micellar catalyst for kilo fold rate acceleration on benzaldehyde to benzoic acid conversion in aqueous media at room temperature: A kinetic approach vol.109, 2013, https://doi.org/10.1016/j.saa.2013.02.019
- Choice of suitable micellar catalyst for 2,2′-bipyridine-promoted chromic acid oxidation of glycerol to glyceraldehyde in aqueous media at room temperature vol.41, pp.5, 2015, https://doi.org/10.1007/s11164-013-1415-6
- Combination of best promoter and micellar catalyst for chromic acid oxidation of 1-butanol to 1-butanal in aqueous media at room temperature vol.124, 2014, https://doi.org/10.1016/j.saa.2013.12.101
- Employment of different spectroscopic tools for the investigation of chromium(VI) oxidation of acetaldehyde in aqueous micellar medium vol.129, pp.5, 2017, https://doi.org/10.1007/s12039-017-1276-4
- Micellar effect on hetero-aromatic nitrogen base promoted chromic acid oxidation of 1.3-propanediol in aqueous media at room temperature vol.225, 2017, https://doi.org/10.1016/j.molliq.2016.11.033
- Combination of Best Promoter and Micellar Catalyst for Cr(VI) Oxidation of Lactose to Lactobionic Acid in Aqueous Medium at Room Temperature vol.51, pp.4, 2014, https://doi.org/10.3139/113.110314
- Rate enhancement via micelle encapsulation for room temperature metal catalyzed Ce(IV) oxidation of formaldehyde to formic acid in aqueous medium at atmospheric pressure: A kinetic approach vol.186, 2013, https://doi.org/10.1016/j.molliq.2013.07.003
- Micellar Catalysis on 1,10-Phenanthroline Promoted Chromic Acid Oxidation of Ethane-1,2-diol in Aqueous Media at Room Temperature vol.56, pp.6, 2012, https://doi.org/10.5012/jkcs.2012.56.6.720
- Selection of Suitable Micellar Catalyst for 1,10-Phenanthroline Promoted Chromic Acid Oxidation of Formic Acid in Aqueous Media at Room Temperature vol.57, pp.6, 2013, https://doi.org/10.5012/jkcs.2013.57.6.703
- Suitable combination of promoter and micellar catalyst for kilo fold rate acceleration on propanol to propionaldehyde conversion in aqueous media vol.20, pp.1, 2014, https://doi.org/10.1016/j.jiec.2013.03.028
- Combination of the most efficient promoter and micellar catalyst for rate enhancement of chromic acid oxidation on 2-butanol to 2-butanone conversion in aqueous media at room temperature vol.41, pp.11, 2015, https://doi.org/10.1007/s11164-014-1908-y
- Micellar Catalysis of Chromic Acid Oxidation of Methionine to Industrially Important Methylthiol in Aqueous Media at Room Temperature vol.50, pp.2, 2013, https://doi.org/10.3139/113.110237
- Optimal Process Condition for Room Temperature Hetero-Aromatic Nitrogen Base Promoted Chromic Acid Oxidation ofp-Chlorobenzaldehyde top-Chlorobenzoic Acid in Aqueous Micellar Medium at Atmospheric Pressure vol.53, pp.1, 2016, https://doi.org/10.3139/113.110414
- A review on the advancement of ether synthesis from organic solvent to water vol.6, pp.73, 2016, https://doi.org/10.1039/C6RA12914E
- Rate enhancement via micelle encapsulation for room temperature metal catalyzed Ce(IV) oxidation of p-chlorobenzaldehyde to p-chlorobenzoic acid in aqueous medium at atmospheric pressure vol.190, 2014, https://doi.org/10.1016/j.molliq.2013.10.029
- Combination of Best Promoter and Micellar Catalyst for Chromic Acid Oxidation of D-Mannitol to Mannose in Aqueous Media vol.50, pp.4, 2013, https://doi.org/10.3139/113.110256