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通过水/液态二氧化碳双相体系实现长链全氟羧酸的高效光化学分解。

Efficient photochemical decomposition of long-chain perfluorocarboxylic acids by means of an aqueous/liquid CO2 biphasic system.

作者信息

Hori Hisao, Yamamoto Ari, Kutsuna Shuzo

机构信息

National Institute of Advanced Industrial Science and Technology (AIST), AIST Tsukuba West, 16-1 Onogawa, Tsukuba 305-8569, Japan.

出版信息

Environ Sci Technol. 2005 Oct 1;39(19):7692-7. doi: 10.1021/es050753r.

Abstract

Photochemical decomposition of persistent and bioaccumulative long-chain (C9-C11) perfluorocarboxylic acids (PFCAs) with persulfate ion (S2O8(2-)) in an aqueous/liquid CO2 biphasic system was examined to develop a technique to neutralize stationary sources of the long-chain PFCAs. The long-chain PFCAs, namely, perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), and perfluoroundecanoic acid (PFUA), which are used as emulsifying agents and as surface treatment agents in industry, are relatively insoluble in water but are soluble in liquid CO2; therefore, introduction of liquid CO2 to the aqueous photoreaction system reduces the interference of colloidal PFCA particles. When the biphasic system was used to decompose these PFCAs, the extent of reaction was 6.4-51 times as high as that achieved in the absence of CO2. In the biphasic system, PFNA, PFDA, and PFUA (33.5-33.6 micromol) in 25.0 mL of water were 100%, 100%, and 77.1% decomposed, respectively, after 12 h of irradiation with a 200-W xenon-mercury lamp; F- ions were produced as a major product, and short-chain PFCAs, which are less bioaccumulative than the original PFCAs, were minor products. All of the initial S2O8(2-) was transformed to SO42-. The system also efficiently decomposed PFCAs at lower concentrations (e.g., 4.28-16.7 micromol of PFDA in 25.0 mL) and was successfully applied to decompose PFNA in floor wax.

摘要

研究了在水/液态二氧化碳双相体系中,过硫酸根离子(S2O8(2-))对持久性和生物累积性长链(C9 - C11)全氟羧酸(PFCA)的光化学分解作用,以开发一种中和长链PFCA固定源的技术。长链PFCA,即全氟壬酸(PFNA)、全氟癸酸(PFDA)和全氟十一酸(PFUA),在工业中用作乳化剂和表面处理剂,它们相对难溶于水,但可溶于液态二氧化碳;因此,将液态二氧化碳引入水性光反应体系可减少胶体PFCA颗粒的干扰。当使用双相体系分解这些PFCA时,反应程度比无二氧化碳时高6.4 - 51倍。在双相体系中,25.0 mL水中的PFNA、PFDA和PFUA(33.5 - 33.6 μmol)在200 W氙汞灯照射12小时后,分别有100%、100%和77.1%被分解;主要产物为F - 离子,生物累积性比原始PFCA低的短链PFCA为次要产物。所有初始的S2O8(2-)都转化为了SO42-。该体系还能有效分解较低浓度的PFCA(例如,25.0 mL中含4.28 - 16.7 μmol的PFDA),并成功应用于分解地板蜡中的PFNA。

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