2007
DOI: 10.1016/j.desal.2006.02.061
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Complex extraction and stripping of H acid wastewater

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Cited by 17 publications
(13 citation statements)
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“…When pH < 7 there is a strong anion association action between the trialkylamine extractant and the organic compounds [35]. The extraction mechanism of trialkylamine in kerosene is mainly based on the ion exchange [35]. The extraction reactions can be described as follows:…”
Section: Theorymentioning
confidence: 99%
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“…When pH < 7 there is a strong anion association action between the trialkylamine extractant and the organic compounds [35]. The extraction mechanism of trialkylamine in kerosene is mainly based on the ion exchange [35]. The extraction reactions can be described as follows:…”
Section: Theorymentioning
confidence: 99%
“…The sulfonic group -SO 3 Na of K-2BP in aqueous solutions of organic compounds is in the state of -SO 3 − . When pH < 7 there is a strong anion association action between the trialkylamine extractant and the organic compounds [35]. The extraction mechanism of trialkylamine in kerosene is mainly based on the ion exchange [35].…”
Section: Theorymentioning
confidence: 99%
See 1 more Smart Citation
“…Although naphthalene sulphonates themselves impart a low acute biotoxicity and have neither mutagenic nor carcinogenic effects, their persistence and mobility in the environment as a result of their physicochemical properties such as their high solubility in water and low octanol-water partition coefficient (Lange et al 1998;Li et al 2006) may cause ecological problems. Due to the deactivating nature of their sulphonated functional groupings (R-SO 3 H), naphthalene sulphonates have an extremely low reactivity against electrophilic addition reactions including microbial degradation (Rieger et al 2002).…”
Section: Industrial Significance Sources and Fate In Natural Watersmentioning
confidence: 99%
“…In this study, anion exchange resin was employed to adsorb H‐acid from the wastewater and other pollutants, including T‐acid (1‐naphthylamine‐3,6,8‐trisulphonic acid) and chromotropic acid (1, 8‐dihydroxy‐3, 6‐naphthalene disulphonic acid) [28].…”
Section: Introductionmentioning
confidence: 99%