Nitrogen-doped TiO2 suspensions in photocatalytic degradation of mecoprop and (4-chloro-2-methylphenoxy)acetic acid herbicides using various light sources
被引:24
作者:
Abramovic, Bijana F.
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Univ Novi Sad, Fac Sci, Dept Chem, Novi Sad 21000, SerbiaUniv Novi Sad, Fac Sci, Dept Chem, Novi Sad 21000, Serbia
Abramovic, Bijana F.
[1
]
Sojic, Daniela V.
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Univ Novi Sad, Fac Sci, Dept Chem, Novi Sad 21000, SerbiaUniv Novi Sad, Fac Sci, Dept Chem, Novi Sad 21000, Serbia
Sojic, Daniela V.
[1
]
Anderluh, Vesna B.
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Univ Novi Sad, Fac Sci, Dept Chem, Novi Sad 21000, SerbiaUniv Novi Sad, Fac Sci, Dept Chem, Novi Sad 21000, Serbia
Anderluh, Vesna B.
[1
]
Abazovic, Nadica D.
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Vinca Inst Nucl Sci, Belgrade 11001, SerbiaUniv Novi Sad, Fac Sci, Dept Chem, Novi Sad 21000, Serbia
Abazovic, Nadica D.
[2
]
Comor, Mirjana I.
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Vinca Inst Nucl Sci, Belgrade 11001, SerbiaUniv Novi Sad, Fac Sci, Dept Chem, Novi Sad 21000, Serbia
Comor, Mirjana I.
[2
]
机构:
[1] Univ Novi Sad, Fac Sci, Dept Chem, Novi Sad 21000, Serbia
The work describes a study of the oxidation power of nitrogen-doped titanium dioxide (TiO2) suspensions for photocatalytic degradation of the herbicides RS-2-(4-chloro-o-tolyloxy) prop ionic acid (mecoprop) and (4-chloro-2methylphenoxy)acetic acid (MCPA) using various light sources. The nitrogen-doped TiO2 crystalline nanopowder was synthesized by calcination of the hydrolysis product of titanium tetraisopropoxide in ammonia. The product was an anatase crystal phase with mean particle diameter 7-15 nm and specific surface area of 121 +/- 1 m(2) g(-1). It showed visible-light photocatalytic activity at about 530 rim. Although nitrogen concentration in nitrogen-doped TiO2 is low (<1 atomic %), it appeared to be about 1.5 times more efficient than TiO2 Degussa P25 when artificial visible light was used for mecoprop and MCPA degradation, and about six times compared to direct photolysis. It was found that the optimal content of nitrogen-doped TiO2 was 4 mg cm(-3). The photodegradation of the herbicide aromatic ring takes place simultaneously with chloride evolution, whereby the reaction in both cases follows first-order kinetics.