Solid phase extraction of uranium(VI) onto benzoylthiourea-anchored activated carbon

A new solid phase extractant selective for uranium(VI) based on benzoylthiourea anchored to activated carbon was developed via hydroxylation, amidation and reaction with benzoyl isothiocyanate in sequence. Fourier transform infrared spectroscopy and total element analysis proved that benzoylthiourea...

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Veröffentlicht in:Journal of hazardous materials 2010-04, Vol.176 (1), p.119-124
Hauptverfasser: Zhao, Yongsheng, Liu, Chunxia, Feng, Miao, Chen, Zhen, Li, Shuqiong, Tian, Gan, Wang, Li, Huang, Jingbo, Li, Shoujian
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container_end_page 124
container_issue 1
container_start_page 119
container_title Journal of hazardous materials
container_volume 176
creator Zhao, Yongsheng
Liu, Chunxia
Feng, Miao
Chen, Zhen
Li, Shuqiong
Tian, Gan
Wang, Li
Huang, Jingbo
Li, Shoujian
description A new solid phase extractant selective for uranium(VI) based on benzoylthiourea anchored to activated carbon was developed via hydroxylation, amidation and reaction with benzoyl isothiocyanate in sequence. Fourier transform infrared spectroscopy and total element analysis proved that benzoylthiourea had been successfully grafted to the surface of the activated carbon, with a loading capacity of 1.2 mmol benzoylthiourea per gram of activated carbon. The parameters that affect the uranium(VI) sorption, such as contact time, solution pH, initial uranium(VI) concentration, adsorbent dose and temperature, have been investigated. Results have been analyzed by Langmuir and Freundlich isotherm; the former was more suitable to describe the sorption process. The maximum sorption capacity (82 mg/g) for uranium(VI) was obtained at experimental conditions. The rate constant for the uranium sorption by the as-synthesized extractant was 0.441 min −1 from the first order rate equation. Thermodynamic parameters (Δ H 0 = −46.2 kJ/mol; Δ S 0 = −98.0 J/mol K; Δ G 0 = −17.5 kJ/mol) showed the adsorption of an exothermic process and spontaneous nature, respectively. Additional studies indicated that the benzoylthiourea-anchored activated carbon (BT-AC) selectively sorbed uranyl ions in the presence of competing ions, Na +, Co 2+, Sr 2+, Cs + and La 3+.
doi_str_mv 10.1016/j.jhazmat.2009.11.005
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Fourier transform infrared spectroscopy and total element analysis proved that benzoylthiourea had been successfully grafted to the surface of the activated carbon, with a loading capacity of 1.2 mmol benzoylthiourea per gram of activated carbon. The parameters that affect the uranium(VI) sorption, such as contact time, solution pH, initial uranium(VI) concentration, adsorbent dose and temperature, have been investigated. Results have been analyzed by Langmuir and Freundlich isotherm; the former was more suitable to describe the sorption process. The maximum sorption capacity (82 mg/g) for uranium(VI) was obtained at experimental conditions. The rate constant for the uranium sorption by the as-synthesized extractant was 0.441 min −1 from the first order rate equation. Thermodynamic parameters (Δ H 0 = −46.2 kJ/mol; Δ S 0 = −98.0 J/mol K; Δ G 0 = −17.5 kJ/mol) showed the adsorption of an exothermic process and spontaneous nature, respectively. 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Fourier transform infrared spectroscopy and total element analysis proved that benzoylthiourea had been successfully grafted to the surface of the activated carbon, with a loading capacity of 1.2 mmol benzoylthiourea per gram of activated carbon. The parameters that affect the uranium(VI) sorption, such as contact time, solution pH, initial uranium(VI) concentration, adsorbent dose and temperature, have been investigated. Results have been analyzed by Langmuir and Freundlich isotherm; the former was more suitable to describe the sorption process. The maximum sorption capacity (82 mg/g) for uranium(VI) was obtained at experimental conditions. The rate constant for the uranium sorption by the as-synthesized extractant was 0.441 min −1 from the first order rate equation. Thermodynamic parameters (Δ H 0 = −46.2 kJ/mol; Δ S 0 = −98.0 J/mol K; Δ G 0 = −17.5 kJ/mol) showed the adsorption of an exothermic process and spontaneous nature, respectively. 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Additional studies indicated that the benzoylthiourea-anchored activated carbon (BT-AC) selectively sorbed uranyl ions in the presence of competing ions, Na +, Co 2+, Sr 2+, Cs + and La 3+.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>19963318</pmid><doi>10.1016/j.jhazmat.2009.11.005</doi><tpages>6</tpages></addata></record>
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subjects Activated carbon
Adsorption
Applied sciences
Benzoylthiourea
Cations
Charcoal - chemistry
Chemical engineering
Exact sciences and technology
Extraction
Hydrogen-Ion Concentration
Hydroxylation
Kinetics
Mathematical analysis
Pollution
Rate constants
Solid phase extraction
Solid Phase Extraction - methods
Solid phases
Sorption
Surface chemistry
Temperature
Thermodynamics
Thiourea - chemistry
Uranium
Uranium - isolation & purification
title Solid phase extraction of uranium(VI) onto benzoylthiourea-anchored activated carbon
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