2006
DOI: 10.1016/j.jhazmat.2006.03.015
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Recovery of nickel and cobalt from organic acid complexes: Adsorption mechanisms of metal-organic complexes onto aminophosphonate chelating resin

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Cited by 64 publications
(41 citation statements)
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References 19 publications
(31 reference statements)
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“…Under analogous conditions the sorption capacity for Cd(II) was 1.1 eq/dm 3 . Recovery of Ni(II) and Co(II) from organic acid complexes using Purolite S 950 was also studied by Deepatana & Valix (2006). They found that sorption capacities for nickel sulphate(VI) for Dowex M4195 (94.51 mg/g), Amberlite IRC 748 (125.03 mg/g) and Ionac SR-5 (79.26 mg/g) are much higher than those for Purolite S-950 in the case of sorption of Ni(II) complexes with citric acid (18.42 mg/g), malic acid (14.45 mg/g) and lactic acid (19.42 mg/g) mainly due to the steric hindrance.…”
Section: Chelating Ion Exchangers With the Phosphonic And Aminophosphmentioning
confidence: 99%
“…Under analogous conditions the sorption capacity for Cd(II) was 1.1 eq/dm 3 . Recovery of Ni(II) and Co(II) from organic acid complexes using Purolite S 950 was also studied by Deepatana & Valix (2006). They found that sorption capacities for nickel sulphate(VI) for Dowex M4195 (94.51 mg/g), Amberlite IRC 748 (125.03 mg/g) and Ionac SR-5 (79.26 mg/g) are much higher than those for Purolite S-950 in the case of sorption of Ni(II) complexes with citric acid (18.42 mg/g), malic acid (14.45 mg/g) and lactic acid (19.42 mg/g) mainly due to the steric hindrance.…”
Section: Chelating Ion Exchangers With the Phosphonic And Aminophosphmentioning
confidence: 99%
“…Intraparticle diffusion equation : q = k int t 1/2 (5) where Q e and q are the amounts of the metal ions adsorbed (mg g −1 ) at equilibrium and at time t (min), respectively, k 1 (min −1 ), k 2 (g mmol −1 min −1 ) and k int (mmol g −1 min −1/2 ) are the rate constants. The parameters of the three equations were tabulated in Table 3.…”
Section: Adsorption Kineticsmentioning
confidence: 99%
“…doi:10.1016/j.jhazmat.2009.01.020 and chelation [5][6][7]. To develop this promising technology, several researchers have obtained some series of chelating resins through the polymerization of conventional chelating monomers such as acrylic acid, methacrylic acid and vinylpyridine [8][9][10].…”
Section: Introductionmentioning
confidence: 99%
“…However, the use of fungi suffers from certain limitations and these include: (i) the need to add organic compounds as a source of carbon and energy to culture the fungi, which increases the cost of future commercial processes [13], (ii) the formation of chelates, which hinders the recovery of dissolved metals [14] and decreases the amount of leached metals, (iii) the phenomenon of biosorption by the fungal biomass [12,[15][16][17] and (iv) electrosorption effects [18], i.e. the attraction of metal cations in solution through electrostatic interactions between the gangue and the cation.…”
Section: Introductionmentioning
confidence: 99%