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In situ hydrothermal growth of a dual-ligand metal-organic framework film on a stainless steel fiber for solid-phase microextraction of polycyclic aromatic hydrocarbons in environmental water samples

机译:在不锈钢纤维上原位水热生长双配位金属有机骨架膜,用于固相微萃取环境水样中的多环芳烃

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摘要

Effective enrichment and determination of polycyclic aromatic hydrocarbons (PAHs) in environmental aqueous solutions is still a major challenge because of their poor solubility and low concentration in the environmental matrix. Solid-phase microextraction (SPME) has been proven to be an effective technique for analyzing trace analytes from environmental samples. Herein, we report the fabrication of a dualligand metal-organic framework (MOF) bio-MOF-1-coated stainless steel fiber via an in situ growth approach for SPME of six PAHs in water samples. Such MOF-based SPME in combination with gas chromatography (GC) gave enhancement factors of 3104-5980, ranges of 10-100 mu g L-1 for Nap, Ace, and Fle, 2.5-100 mu g L-1 for Phen, 0.1-100 mu g L-1 for FluA and Pyr, detection limits (S/N = 3) of 0.02-5.57 mg L-1, and quantitation limits (S/N = 10) of 0.14-17.2 mu g L-1 for the studied PAHs. The recoveries obtained by spiking 10 mu g L-1 PAHs in water samples ranged from 80% to 115%. The results showed that p-p interaction with biphenyldicarboxylate and pi-complexation between aromatic rings and the pyrimidine in the pores of bio-MOF-1 play significant roles in the extraction of PAHs.
机译:在环境水溶液中有效富集和测定多环芳烃(PAHs)仍然是一个主要挑战,因为它们在环境基质中的溶解性差和浓度低。固相微萃取(SPME)已被证明是一种分析环境样品中痕量分析物的有效技术。在此,我们报告了通过原位生长方法对水样品中的六个PAHs进行双配体金属有机骨架(MOF)生物-MOF-1涂层不锈钢纤维的制造。将此类基于MOF的SPME与气相色谱(GC)结合使用可得出增强因子3104-5980,Nap,Ace和Fle的L-1范围为10-100μgL-1,Phen的2.5-100μgL-1, FluA和Pyr为0.1-100μg L-1,检出限(S / N = 3)为0.02-5.57 mg L-1,定量限(S / N = 10)为0.14-17.2μgL-1用于研究的PAH。在水样中加标10微克L-1 PAHs所获得的回收率在80%至115%之间。结果表明,在生物MOF-1的孔中,与联苯二甲酸的p-p相互作用以及芳香环与嘧啶之间的pi络合在PAHs的提取中起重要作用。

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