Multifunctional capacity of CoMnFe-LDH/LDO activated peroxymonosulfate for p-arsanilic acid removal and inorganic arsenic immobilization: Performance and surface-bound radical mechanism

2022 ◽  
Vol 806 ◽  
pp. 150379
Author(s):  
Cheng Ye ◽  
Jing Deng ◽  
Lingyi Huai ◽  
Anhong Cai ◽  
Xiao Ling ◽  
...  
2021 ◽  
Author(s):  
Qiang Peng ◽  
Wenze Xu ◽  
Weixiao Qi ◽  
Chengzhi Hu ◽  
Huijuan Liu ◽  
...  

Abstract Phenylarsonic acid compounds, which were widely used in poultry and swine production, are emerging contaminants due to their considerable solubility in water and the highly toxic inorganic arsenic species forming potential during their biotic and abiotic degradation in the natural environment. Herein, we investigated the optimal conditions to treat typical organoarsenic contaminants ( p -arsanilic acid ( p -ASA) and phenylarsonic acid (PAA)) in aqueous solution based on Fenton-coagulation process for oxidizing them and capturing the released inorganic arsenic, and elucidated the influence mechanism of substituted amino group on removal. Results showed that the pH value and the dosage of H 2 O 2 and Fe 2+ significantly influenced the performance of the oxidation and coagulation processes. The optimal conditions for removing 20mg L -1 -As in this research were: 40mg L -1 Fe 2+ and 60mg L -1 H 2 O 2 (the mass ratio of Fe 2+ /H 2 O 2 = 1.5), initial solution pH of 3.0 and final solution pH of 5.0 adjusting after 30 min Fenton oxidation reaction. Meanwhile, the substituted amino group observably influence the oxidation and coagulation performance of phenylarsonic acid compounds. Amino group could make phenylarsonic acid compounds more easily be attacked by ·HO and supply more binding sites for forming complexes with Fe 3+ hydrolysates, resulting in higher oxidation rate and better coagulation performance.


Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
C Ubonnuch ◽  
S Ruangwises ◽  
N Ruangwises ◽  
W Gritsanapan
Keyword(s):  

1961 ◽  
Vol 20 (4) ◽  
pp. 768-773 ◽  
Author(s):  
I. D. Smith ◽  
E. M. Kiggins ◽  
H. S. Perdue ◽  
J. C. Holper ◽  
D. V. Frost

2020 ◽  
Author(s):  
Josh MacMillan ◽  
Katherine Marczenko ◽  
Erin Johnson ◽  
Saurabh Chitnis

The addition of Sb-H bonds to alkynes was reported recently as a new hydroelementation reaction that exclusively yields anti-Markovnikov <i>Z</i>-olefins from terminal acetylenes. We examine four possible mechanisms that are consistent with the observed stereochemical and regiochemical outcomes. A comprehensive analysis of solvent, substituent, isotope, additive, and temperature effects on hydrostibination reaction rates definitively refutes three ionic mechanisms involving closed-shell charged intermediates. Instead the data support a fourth pathway featuring neutral radical Sb<sup>II</sup> and Sb<sup>III</sup> intermediates. Density Functional Theory (DFT) calculations are consistent this model, predicting an activation barrier that is within 1 kcal mol<sup>-1</sup> of the experimental value (Eyring analysis) and a rate limiting step that is congruent with experimental kinetic isotope effect. We therefore conclude that hydrostibination of arylacetylenes is initiated by the generation of stibinyl radicals, which then participate in a cycle featuring Sb<sup>II</sup> and Sb<sup>III</sup> intermediates to yield the observed <i>Z</i>-olefins as products. This mechanistic understanding will enable rational evolution of hydrostibination as a methodology for accessing challenging products such as <i>E</i>-olefins.


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