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Perfluorooctane sulfonate (PFOS) removal with Pd-0Fe(0) nanoparticles: Adsorption or aqueous Fe-complexation, not transformation?

机译:用Pd-0 / nFe(0)纳米颗粒去除全氟辛烷磺酸(PFOS):吸附或水Fe复合,不是转化?

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PFOS removal at 6 and 21days (d) when reacted with palladium coated zero valent iron nanoparticles (Pd0Fe0 NPs) was quantified as a function of pH (3.6, 5.5, and 8.7) and temperature (22, 45 and 70 degrees C). PFOS concentrations were measured in aqueous phases and NP extracts. The greatest PFOS removal occurred at 6 d with the lowest pH and highest temperature; however, recovered PFOS increased at 21 d. Furthermore, neither F- nor SO42- (from SO32- cleavage) generation was observed indicating the absence of PFOS transformation. X-ray diffraction analysis of PFOS-reacted NPs at 45 degrees C revealed generation of FeO(OH) on the NPs at 21 d, which was concomitant with subsequent increases in PFOS recovery. Under anaerobic conditions, strongly adsorbing Fe(OH)(3) is formed which can then transform to less sorptive FeO(OH) via Fe2+ catalyzed transformation. In the process of exploring causes for apparent PFOS removal with Pd0Fe0 NPs, PFOS as well as other perfluoroalkyl acids (PFAAs) were found to form aqueous-phase complexes with Fe(II/III) which can reduce their quantifiable levels. PFOS-Fe complexation was greater with Fe(III) and increased with Fe concentration and decreasing pH. Complexation was also greater for longer chain perfluoroalkyl acids and complexation of PFNA was greater than for PFOS. (C) 2017 Elsevier B.V. All rights reserved.
机译:当与钯包覆的零价铁纳米颗粒(Pd0 / nFe0 NPs)反应时,在第6天和第21天(d)的PFOS去除量随pH(3.6、5.5和8.7)和温度(22、45和70摄氏度)的变化而定量。在水相和NP提取物中测量PFOS浓度。在最低pH和最高温度的6 d内,最大的PFOS去除率最高。但是,回收的全氟辛烷磺酸在21天时有所增加。此外,未观察到F-或SO42-(来自SO32-裂解)的产生,表明不存在PFOS转化。在45摄氏度下对PFOS反应的NP进行X射线衍射分析表明,在21 d时在NP上生成了FeO(OH),这与随后PFOS回收率的提高同时发生。在厌氧条件下,形成强烈吸附的Fe(OH)(3),然后可以通过Fe2 +催化的转化转化为吸附性较弱的FeO(OH)。在探索用Pd0 / nFe0 NP去除明显的PFOS的原因的过程中,发现PFOS以及其他全氟烷基酸(PFAA)与Fe(II / III)形成了水相复合物,可以降低其定量水平。 PFOS-Fe的络合度随Fe(III)的增加而增加,随Fe浓度的增加和pH的降低而增加。长链全氟烷基酸的络合度也更大,PFNA的络合度比PFOS更大。 (C)2017 Elsevier B.V.保留所有权利。

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