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Removal of typical perfluorinated surfactants from water using some conventional adsorbents

机译:使用某些常规吸附剂从水中去除典型的全氟表面活性剂

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Perfluorinated surfactants such as Perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) have increasingly attracted global concerns in recent years due to their global distribution, persistence, strong bioaccumulation and potential toxicity. They had been detected in wastewater, surface water, groundwater and even tap water throughout the world. In 2009, PFOS has been listed as one of persistent organic pollutants in COP4. As industrial wastewater has been implicated as a point source for PFOS and PFOA entering into natural waters, source control of PFOS and PFOA release into water environment becomes crucial. Some conventional techniques including biological degradation, oxidation and reduction are difficult to destruct PFOS and PFOA in ambient environments due to their stable properties, while adsorption would be an effective technique to remove them from aqueous solution.In this study, the feasibility of using powder activated carbon (PAC), granular activated carbon (GAC) and different resins to remove PFOS and PFOA from water was investigated. The sorption behaviors including sorption kinetics, isotherms, effect of solution pH and temperature were studied in detail, and the possible sorption mechanisms were discussed.In the sorption kinetics, it was found that the adsorption of PFOS and PFOA on the GAC very slow and the sorption equilibrium was achieved after at least 168 h, while the sorption equilibrium time was only about 4 h using the PAC, indicating that the adsorbent size significantly affected the sorption velocity of PFOS and PFOA. In contrast, the sorption kinetic of PFOS and PFOA on the resins was dependent on their matrix and functional groups. The resin matrix had significant impact on the sorption kinetic. The adsorption of PFOS on the polystyrene divinylbenzene based anion exchange resins such as AI400 was very slow and the sorption equilibrium was not obtained after 10 days, which was due to the strong hydrophobic property of the matrix and the difficult diffusion of PFOS molecules into the intraparticle pores. When the polyacrylic ester based anion exchange resins such as IRA67 were used to remove PFOS, the sorption equilibrium was achieved after 48 h, while the sorption equilibrium on the nonionic resin XAD7 was reached after 24 h. The functional groups including quaternary ammonium and polyamine on the resins were favorable for PFOS removal. The resin pores had little effect on the sorption kinetic of PFOS. The sorption kinetics of PFOS and PFOA on the activated carbon and resins can be described well using the pseudo-second-order and Elovich equation, and the intraparticle diffusion model can well fit their sorption on the GAC and AI400 in the initial stage.
机译:近年来,全氟表面活性剂(例如全氟辛烷磺酸盐(PFOS)和全氟辛酸盐(PFOA))因其全球分布,持久性,强大的生物蓄积性和潜在毒性而日益引起全球关注。在全世界的废水,地表水,地下水甚至自来水中都检测到了它们。 2009年,全氟辛烷磺酸被列为第四届缔约方会议的持久性有机污染物之一。由于工业废水被认为是全氟辛烷磺酸和全氟辛烷磺酸进入自然水体的重要来源,因此全氟辛烷磺酸和全氟辛烷磺酸向水环境的排放源头控制变得至关重要。由于其稳定的性能,一些常规技术(包括生物降解,氧化和还原)在环境中很难破坏PFOS和PFOA,而吸附将是从水溶液中去除它们的有效技术。 在这项研究中,研究了使用粉末活性炭(PAC),颗粒状活性炭(GAC)和不同的树脂从水中去除PFOS和PFOA的可行性。详细研究了吸附行为,包括吸附动力学,等温线,溶液pH和温度的影响,并探讨了可能的吸附机理。 在吸附动力学中,发现PFOS和PFOA在GAC上的吸附非常缓慢,并且在至少168 h后才达到吸附平衡,而使用PAC的吸附平衡时间仅为约4 h,这表明吸附剂粒径显着影响全氟辛烷磺酸和全氟辛烷磺酸的吸附速度。相反,PFOS和PFOA在树脂上的吸附动力学取决于它们的基质和官能团。树脂基质对吸附动力学有显着影响。 PFOS在基于聚苯乙烯二乙烯基苯的阴离子交换树脂(如AI400)上的吸附非常缓慢,并且在10天后未达到吸附平衡,这是由于基质的强疏水性以及PFOS分子难以扩散到颗粒内引起的毛孔。当使用聚丙烯酸酯基阴离子交换树脂(例如IRA67)去除PFOS时,在48小时后达到吸附平衡,而在24小时后达到非离子树脂XAD7的吸附平衡。树脂上的季铵盐和多胺等官能团对于PFOS的去除非常有利。树脂孔对全氟辛烷磺酸的吸附动力学影响很小。 PFOS和PFOA在活性炭和树脂上的吸附动力学可以使用拟二阶和Elovich方程很好地描述,并且颗粒内扩散模型可以很好地拟合它们在初始阶段对GAC和AI400的吸附。

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