2015
DOI: 10.1016/j.apsusc.2015.06.072
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A novel collector 2-ethyl-2-hexenoic hydroxamic acid: Flotation performance and adsorption mechanism to ilmenite

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Cited by 62 publications
(13 citation statements)
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“…According to [1], hydroxamic acid (HA), represented by the general formula, R-CO-NHOH, is a compound derived from oxoacid by replacing the –OH in it by –NHOH, and its hydrocarbyl derivatives. The HAs are much weaker acids as compared with the corresponding carboxylic acids despite having identical carbon chains, however, they possess stronger abilities for selectively chelating metal ions [2]. As a metal binding group, HA are also widely used as a metalloenzyme inhibitor, including tyrosinase inhibitors [3], histone deacetylase inhibitors [4,5,6,7], and HIV-integrase inhibitors [8].…”
Section: Introductionmentioning
confidence: 99%
“…According to [1], hydroxamic acid (HA), represented by the general formula, R-CO-NHOH, is a compound derived from oxoacid by replacing the –OH in it by –NHOH, and its hydrocarbyl derivatives. The HAs are much weaker acids as compared with the corresponding carboxylic acids despite having identical carbon chains, however, they possess stronger abilities for selectively chelating metal ions [2]. As a metal binding group, HA are also widely used as a metalloenzyme inhibitor, including tyrosinase inhibitors [3], histone deacetylase inhibitors [4,5,6,7], and HIV-integrase inhibitors [8].…”
Section: Introductionmentioning
confidence: 99%
“…There is a significant decrease in the recovery of pyrrhotite using sodium butyl xanthate (SBX) as a collector when ET = 24 h [19,23]. Hydroxamic acids, R-CO-NHOH (R, alkyl/aryl group), are much weaker acids than the corresponding carboxylic acids, in the identical carbon chain, but possess stronger abilities in selectively chelating metal ions [24]. Hydroxamic acids can chelate with metal cations (e.g., Cu 2+ , Fe 3+ , Al 3+ ) to form hydrophobic metal chelates [24,25], and the chelation reaction for hydroximic acids to metal cation can form an "O, N" four-ring chelate and/or an "O, O" five-ring chelate (the chelate products are shown in Figure 1).…”
Section: Introductionmentioning
confidence: 99%
“…Hydroxamic acids, R-CO-NHOH (R, alkyl/aryl group), are much weaker acids than the corresponding carboxylic acids, in the identical carbon chain, but possess stronger abilities in selectively chelating metal ions [24]. Hydroxamic acids can chelate with metal cations (e.g., Cu 2+ , Fe 3+ , Al 3+ ) to form hydrophobic metal chelates [24,25], and the chelation reaction for hydroximic acids to metal cation can form an "O, N" four-ring chelate and/or an "O, O" five-ring chelate (the chelate products are shown in Figure 1). Since the tension of the four-ring chelate is relatively high, and the stability is poor, the chelate product is mainly a five-ring chelate.…”
Section: Introductionmentioning
confidence: 99%
“…Currently, most REEs are extracted from bastnaesite ((Ce,La)CO 3 F) (Chelgani et al, 2015;Yosry, 1990), which is recovered from rare earth ores by flotation. Typically, hydroxamic acids are used as bastnaesite collectors (Xu, 2015;Ren, 1997;Mousumi and Venugopal, 2016). Research into the mechanism of interaction between hydroxamic acids and bastnaesite is important for improving the recoveries of bastnaesite.…”
mentioning
confidence: 99%