共查询到19条相似文献,搜索用时 93 毫秒
1.
串联液质联用仪测定水中全氟辛酸和全氟辛烷磺酸的影响因素分析 总被引:1,自引:0,他引:1
《化学世界》2017,(1)
对HPLC-MS/MS方法测定水中全氟辛酸(PFOA)和全氟辛烷磺酸(PFOS)过程中PFOA和PFOS峰面积的影响因素进行了研究。结果表明在一定的分析条件下PFOA和PFOS分别在保留时间2.08和2.33min处出现明显的色谱峰,随着样品的pH值升高,PFOA和PFOS峰面积逐渐增大,pH值为5.0的情况下,PFOA和PFOS峰面积达到极大值,随pH值增大呈现减小趋势。pH值5.0下PFOA峰面积比pH值1.5下PFOA峰面积大60.3%,相应的PFOS峰面积大32.5%。相同pH值情况下,PFOA、PFOS浓度与峰面积呈良好线性关系。水、甲醇、乙腈作为稀释溶剂对PFOA和PFOS峰面积没有明显影响。聚四氟乙烯、混合纤维等对PFOA和PFOS没有吸附,但尼龙滤膜对PFOA和PFOS有较强吸附。计算结果表明磺酸基与酰胺基团的结合能略大于羧基与酰胺基团的结合能,这可能是尼龙对PFOS吸附能力大于对PFOA吸附能力的原因之一。 相似文献
2.
3.
4.
5.
6.
7.
8.
10.
全氟辛酸(PFOA)和全氟辛烷磺酸(PFOS)是一类新型难降解的持久性污染物。由于在环境中有很高的生物蓄积性、多种毒性和持久稳定性,近年来PFOA/PFOS去除技术的相关研究得到国内外学者的广泛关注和重视。针对PFOA/PFOS在环境中的污染状况及各种去除技术的研究进展进行了综述,并对当前各种去除技术存在的问题进行了分析和探讨。 相似文献
11.
12.
合成一系列全氟辛酸二价盐(M(PFOA)_2,M~(2+)=Mg~(2+),Ca~(2+),Sr~(2+),Ba~(2+))和全氟丁酸二价盐(M(PFBA)_2),并测定其在水、二甲基亚砜(DMSO)和乙二醇(EG)中的表面张力,同时测定了全氟辛酸(PFOA)和全氟丁酸(PFBA)分别与三价金属盐(LaCl_3和FeCl_3)组成的混合物在水溶液中的表面张力。结果表明,与相应的钾盐相比,M(PFOA)_2和M(PFBA)_2具有更高的表面活性,而全氟羧酸(PFOA或PFBA)与三价金属盐的混合物未见表面活性显著提高。M(PFOA)_2可作为降低PFOA盐使用量的重要方法加以应用。 相似文献
13.
Synthesis of a perfluorooctanoic acid molecularly imprinted polymer for the selective removal of perfluorooctanoic acid in an aqueous environment 下载免费PDF全文
Perfluorooctanoic acid (PFOA) contamination in the environment is a global problem. The aqueous phase is the main medium for PFOA because of its moderate solubility. Adsorption is a feasible way to remove PFOA because of its chemical and biological stability. In this study, a new type of molecularly imprinted polymer (MIP) for the selective adsorption of PFOA in aqueous solutions was synthesized by the precipitation polymerization method with PFOA as the template molecule after optimization. The adsorption kinetics and isotherms of the MIP adsorbent toward PFOA were studied, and the effects of the pH and cations on the adsorption were investigated with batch experiments. The results show that acrylamide (AAM) was the best functional monomer, and the optimal molar ratio of PFOA to AAM to ethylene glycol dimethacrylate (crosslinker) was 1:6:25. The optimized MIP adsorbent had a high affinity for PFOA, and the uptake percentage by the MIP adsorbent was 1.3–2.5 times that of the nonimprinted polymer (NIP) when PFOA existed alone. A maximum PFOA sorption capacity of 5.45 mg/g based on the Langmuir isotherm model was achieved with the MIP adsorbent. The MIP adsorbent exhibited a high selectivity for PFOA over competitive compounds (other perfluorinated alkyl carboxylic and sulfonic acids), whereas the NIP did not. Approximately 90% of the PFOA in the mixture was removed by the MIP adsorbent; this was 18 times that of the NIP. Moreover, the regenerability of the MIP adsorbent was confirmed in five sequential adsorption–desorption cycles without a significant reduction in the PFOA uptake. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43192. 相似文献
14.
15.
《分离科学与技术》2012,47(10):1473-1478
The abundance of perfluorooctanoic acid (PFOA) in the aquatic environment makes it important to understand the influence of important parameters affecting the partition of PFOA onto sediment. With a focus on the influence by dissolved organic matter (DOM), we investigated the sorption of PFOA to river sediment downstream of a semiconductor and optoelectronic industrial complex that discharged wastewater with a considerable amount of PFOA in it. The dominant components of the sediment were silica oxide (~14%) and iron oxide (~2%). The sorption density of PFOA was not significantly affected by solution pH and ionic strength. The combinations of low pH-high ionic strength and high pH-low ionic strength favored partitioning of PFOA to the sediment. The sorption density of PFOA to sediment ranged from 0.41 to 1.43 µg/m2, with the presence of DOM in the aqueous phase reducing the affinity of PFOA toward the sediment. The sorption of PFOA seemed to be facilitated not by electrostatic but by hydrophobic interactions. The PFOA-sediment sorption equilibration required a duration exceeding 12 d. This study revealed DOM as an important solution-specific parameter in sorption studies. The influence of DOM on PFOA sorption provides a useful reference to understand PFOA partition in the aqueous environment. Supplemental materials are available for this article. Go to the publisher's online edition of Separation Science & Technology to view the free supplemental file. 相似文献
16.
17.
18.
Huu-Tuan Do Lan-Anh Phan Thi Ngoc Han Dao Nguyen Chao-Wei Huang Quyet Van Le Van-Huy Nguyen 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2020,95(10):2569-2578
A perfluorooctanoic acid (PFOA), as the most important representative of perfluorocarboxylic acids (PFCAs), is environmentally persistent and bioaccumulative. Among treatment techniques for PFOA decomposition, photocatalytic degradation of PFOA has received considerable attention. A series of candidate photocatalytic materials, including TiO2-, carbonaceous-, Ga2O3-, In2O3-based, etc., have been successfully proposed to eliminate PFOA. Overall, there are two types of mechanisms for photocatalytic degradation of PFCAs, including conventional mechanism and charge transfer mechanism. For a conventional mechanism, the mechanism of PFOA photodegradation over bulk TiO2 via two pathways: photo-redox and β-scission. For the charge transfer mechanism, the PFOA degradation pathway in water-soluble H3PW12O40 is mainly via charge-transfer excited complex ([PW12O40]3−*). Finally, attention on critical challenges and prospects for photodegradation of PFOA are also intensified. © 2020 Society of Chemical Industry 相似文献