2015
DOI: 10.1007/s10953-015-0418-x
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Ternary Liquid–Liquid Equilibria for the System 2-Methoxy-2-methylpropane + m-Cresol + Water at 298.15 and 313.15 K: Experimental Data and Correlation

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Cited by 13 publications
(8 citation statements)
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“…Wastewater containing such a high concentration of phenol must be pretreated to reduce phenolic content before the wastewater flows into the biochemical treatment section . For removing and recycling phenol from wastewater, solvent extraction is one of the most effective and economical methods to deal with it. The extraction process can be carried out continuously or intermittently, and the amount of treated water is relatively large.…”
Section: Introductionmentioning
confidence: 99%
“…Wastewater containing such a high concentration of phenol must be pretreated to reduce phenolic content before the wastewater flows into the biochemical treatment section . For removing and recycling phenol from wastewater, solvent extraction is one of the most effective and economical methods to deal with it. The extraction process can be carried out continuously or intermittently, and the amount of treated water is relatively large.…”
Section: Introductionmentioning
confidence: 99%
“…The key problem to design a liquid-liquid extraction process is to develop an appropriate extractant with low water solubility, low price and high efficiency to separate cresols from water. However, such study or data is quite scarce at present, with just a few solvents (or extractants) having been reported [20][21][22][23][24]: at 298.2 K, the distribution coefficient (D) and selectivity (S) of methyl tert-butyl ether for cresols are 800~1200 and 3500~13700, those of methyl isopropyl ketone are 390~1450 and 1300~7800 and those of methyl propyl ketone are 530~1450 and 1900~8900. As a polar organic solvent, Mesityl oxide have shown high efficiency in extracting phenol from the aqueous solution [26].…”
Section: Introductionmentioning
confidence: 99%
“…Hence, quite a few studies have been performed for such purpose. Lv et al reported the LLE data of ternary systems (methyl butyl ketone (MBK) + cresols + water) at (298.2 and 313.2) K. LLE data for the ternary systems methyl isobutyl ketone (MIBK) + o - or p -cresol + water, butyl acetate + o - or p -cresol + water, and isoamyl acetate + o - or p -cresol + water at 303.2 K were published by Telkikar et al Luo et al studied the LLE of ternary systems of methyl tert -butyl ether + o -, m -, p -cresol + water, and Martin et al studied the water + o -, m -, or p -cresol + heptane or octane systems. Among these extractants, MIBK has been used in some industrial plants.…”
Section: Introductionmentioning
confidence: 99%