Effects of titania nanoparticles on phosphorus fractions and its release in resuspended sediments under UV irradiation

被引:17
|
作者
Luo, Zhuanxi [1 ]
Wang, Zhenhong [2 ]
Li, Qingzhao [1 ]
Pan, Qikun [1 ]
Yan, Changzhou [1 ]
机构
[1] Chinese Acad Sci, Inst Urban Environm, Key Lab Urban Environm & Hlth, Xiamen 361021, Peoples R China
[2] Zhangzhou Normal Univ, Dept Chem & Environm Sci, Zhangzhou 363000, Peoples R China
关键词
Nanoparticle; TiO2; Photolysis; Photocatalysis; Organic matter; DISSOLVED ORGANIC-CARBON; PHOTOCATALYTIC DEGRADATION; ENGINEERED NANOPARTICLES; PHOTOCHEMICAL PRODUCTION; PARTICLE-SIZE; LOWER REACHES; DIOXIDE; LAKE; TIO2; ADSORPTION;
D O I
10.1016/j.jhazmat.2009.09.077
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Little is known about the effects of nano-TiO2 On the transformation and transport of phosphorus (P) in resuspended sediments. Chemical sequential extraction was used to investigate P fractions and its release in resuspended sediments under the influence of nano-TiO2 and UV irradiation. The results showed that the contents of sediment P in all fractions decreased with increasing nano-TiO2 concentration in UV irradiation, while increased in the dark controls. Furthermore, P release from all fractions was greater in UV irradiation than in the controls. Elevated concentrations (10-50 mg L-1) of nano-TiO2 in UV irradiation significantly facilitated the release of P from organic and Fe oxide fractions, possibly resulting from the partial photo-degradation of organic matter and photochemical transformation of Fe oxides. Apparently, nano-TiO2 in UV irradiation did not immobilize the loosely sorbed P and reductant soluble P release from the resuspended sediments, possible because (1) some of P released from those fractions were refurnished by the P released from OM; (2) photocatalysis of nano-TiO2 reduced binding capacity of the resuspended sediments. Our results suggest that the photocatalysis of nano-TiO2 may offer the potential to regulate the transformation and transport of sediment P in the aquatic environment. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:477 / 483
页数:7
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