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Oligomerization of 3-substituted quinolines by catalytic activity of soybean peroxidase as a wastewater treatment. Product formation and computational studies
被引:14
|作者:
Mashhadi, Neda
[1
]
Taylor, Keith E.
[1
]
Biswas, Nihar
[2
]
Meister, Paul
[1
]
Gauld, James W.
[1
]
机构:
[1] Univ Windsor, Dept Chem & Biochem, 401 Sunset Ave, Windsor, ON N9B 3P4, Canada
[2] Univ Windsor, Dept Civil & Environm Engn, 401 Sunset Ave, Windsor, ON N9B 3P4, Canada
基金:
加拿大自然科学与工程研究理事会;
关键词:
Wastewater treatment;
Soybean peroxidase;
Computational analysis;
Product;
Quinoline;
HORSERADISH-PEROXIDASE;
ELECTROCHEMICAL OXIDATION;
AROMATIC-HYDROCARBONS;
REMOVAL;
POLYMERIZATION;
DERIVATIVES;
POTENTIALS;
METABOLISM;
PROTONS;
LACCASE;
D O I:
10.1016/j.cej.2019.01.184
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Although heterocyclic aromatics make up a vast group of water contaminants, the effect of enzyme on this class of recalcitrant compounds is largely unknown. Here, the feasibility of treatment of selected quinolines with soybean peroxidase is demonstrated and the effects of the most important parameters; pH, enzyme concentration, and peroxide concentration are optimized for each compound. 3-hydroxy and 3-aminoquinoline were found to be substrates amenable to >= 94% removal with pH optima of 8.6 and 5.6, respectively. In order to identify the transformation products of such treatment, the solution and precipitate after enzymatic treatment were analyzed by mass spectrometry to find that the dominant products were dimers and trimers from oxidative radical coupling. In addition, for 3-aminoquinoline azo-linked dimers and trimers were found. Computational techniques used to investigate the influence of redox potential and ionization energy of pollutants on their treatability by SBP showed a possible threshold between substrates and non-substrates. Computed spin densities were used to predict the regiochemistry of the radical coupling reaction.
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页码:340 / 348
页数:9
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