2011
DOI: 10.3103/s1068364x11080072
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Extractive rectification by means of sulfolane in chemical technology: A review

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Cited by 5 publications
(5 citation statements)
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“…Formally, sulfolane is a cyclic sulfone, containing a four-membered carbon ring and sulfonyl functional group (R2SO2) with a sulfur atom double-bonded to two oxygen atoms with a quite large dipole moment (μ=4.7 debye), dielectric constant (ευ=43.4) and low vapor pressure [12,13]. The structure of sulfolane with its zwitterionic and dritterionic resonance structures is illustrated in [14,15]. Sulfolane is the preferred solvent for these processes due to its satisfactory selectivity for the aromatics of interest, low boiling temperature and its capacity for dissolving large quantities of aromatics in relatively low quantities of solvent -the sulfolane extraction process is less expensive to operate than similar processes using other solvents.…”
Section: Beware Of Sulfolanementioning
confidence: 99%
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“…Formally, sulfolane is a cyclic sulfone, containing a four-membered carbon ring and sulfonyl functional group (R2SO2) with a sulfur atom double-bonded to two oxygen atoms with a quite large dipole moment (μ=4.7 debye), dielectric constant (ευ=43.4) and low vapor pressure [12,13]. The structure of sulfolane with its zwitterionic and dritterionic resonance structures is illustrated in [14,15]. Sulfolane is the preferred solvent for these processes due to its satisfactory selectivity for the aromatics of interest, low boiling temperature and its capacity for dissolving large quantities of aromatics in relatively low quantities of solvent -the sulfolane extraction process is less expensive to operate than similar processes using other solvents.…”
Section: Beware Of Sulfolanementioning
confidence: 99%
“…In fact, pure sulfolane under standard operating conditions is considered to be a stable compound and non-aggressive to steel, but sulfolane systems, if contaminated by traces of oxygen and at typical process conditions (170-180ºC), may lead to sulfolane decomposition and formation of Due to its combination of physical and chemical properties (inertness and stability), sulfolane is a selective solvent in liquid-liquid and liquid-vapour extraction processed, used for the removal of close-boiling alkanes from cycloalkanes (C 5 -C 10 derived from petroleum fractions) or for the separation of compounds with different degree of saturation and polarity in the extractive rectification of arenes (BTX-benzene, toluene, xylene) from non-aromatic saturated hydrocarbon mixtures) [14,15]. Sulfolane is the preferred solvent for these processes due to its satisfactory selectivity for the aromatics of interest, low boiling temperature and its capacity for dissolving large quantities of aromatics in relatively low quantities of solvent-the sulfolane extraction process is less expensive to operate than similar processes using other solvents.…”
Section: Beware Of Sulfolanementioning
confidence: 99%
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“…Regarding the operational costs and limitations of SFL-containing soil/water chemical and/or biological remediation, a key question should be raised about the reasons for unintentional sulfolane leakages into the ecosystem as the extractive liquid is industrially used and regenerated in the closed loop [21]. Moreover, under standard operating conditions, pure SFL is regarded to be non-aggressive to steel, however, small quantities of oxidizing agents (e.g., chlorates, nitrates, peroxides), oxygen or water can induce corrosion processes with the formation of aggressive (by)-products, for instance, SO 2 that is subsequently oxidized to H 2 SO 3 [22].…”
Section: Introductionmentioning
confidence: 99%
“…Due to its satisfactory selectivity, low boiling temperature, and its capacity for dissolving large quantities of aromatics, sulfolane is the preferred solvent for liquid-liquid and liquid-vapor extraction processes when separating compounds with various degrees of saturation and polarity in the extractive rectification of BTX (benzene, toluene, xylene) mixture from the non-aromatic saturated hydrocarbons [8,9,10].…”
Section: Introductionmentioning
confidence: 99%