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Mechanism of persulfate activation with CuO for removing cephalexin and ofloxacin in water

机译:用CuO去除Cephalexin和水中氧氟沙星的过硫酸盐活化机制

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CuO was synthesized by a simple hydrothermal method and investigated as a heterogeneous activator of persulfate for the degradation of cephalexin and ofloxacin. X-ray photo-electron spectroscopy and hydrogen temperature-programmed reduction measurements reveal that CuO contains two types of Cu2+: one has more electron deficiency (named as Cu2+-h) and the other has relatively higher electron density (named as Cu2+-l). Electron paramagnetic resonance and radical scavenging experiments demonstrate that (SO4-)-S-center dot and O-center dot(2)- are responsible for the efficient degradation of cephalexin and ofloxacin, respectively. (SO4-)-S-center dot can be produced through the electron transfer from Cu2+-l to PS and the cleavage of peroxy bond, while O-center dot(2)- can be produced via the electron transfer from PS to Cu2+-h and the cleavage of S-O bond. Finally, the degradation intermediates were identified by liquid chromatograph-mass spectrometry. This study proposed a novel mechanism for the activation of persulfate with CuO, which is useful for the rational design of persulfate activator for controlling the production of active species.
机译:通过一种简单的水热法合成CuO,并作为过硫酸盐的过硫酸盐的异质活化剂进行合成,用于Cephalexin和α氧氟沙星的降解。 X射线照片 - 电子光谱和氢气温度编程的减少测量表明,CuO含有两种类型的Cu2 +:一个具有更多的电子缺陷(命名为Cu2 + -H),另一个具有相对较高的电子密度(命名为Cu2 + -L) 。电子顺磁共振和自由基清除实验表明(SO4 - ) - S中心点和O中心点(2) - 负责分别有效降解头孢氨酸和氧氟沙星的高效降解。 (SO4 - ) - S中心点可以通过来自Cu2 + -L的电子转移来制造和过氧键的切割,同时O中心点(2) - 可以通过从PS到Cu2 +的电子转移产生 - h和so bond的切割。最后,通过液相色谱 - 质谱法鉴定了降解中间体。该研究提出了一种用于激活过硫酸盐的新机制,这对于用于控制活性物质的过硫酸盐活化剂的合理设计是有用的。

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