Efficient analysis of polycyclic aromatic hydrocarbons by dispersive-µ-solid-phase extraction using silica-based nanostructured sorbent phases coupled to gas chromatography-mass spectrometry

IF 5.2 Q1 CHEMISTRY, ANALYTICAL
Camila Scheid , Wendell Mello , Silvio Buchner , Edilson Valmir Benvenutti , Monique Deon , Josias Merib
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引用次数: 2

Abstract

In this study, SBA-15 mesoporous silica has been investigated as sorbent phase for the extraction and determination of 10 polycyclic aromatic hydrocarbons (PAHs) in environmental water samples for the first time. The extraction step was performed through a dispersive-µ-solid-phase extraction (D-µ-SPE) followed by gas chromatography coupled to mass spectrometry (GC-MS). In particular, the surface of SBA-15 was chemically bonded to different functional groups (aminopropyl, phenyl, octyl and octadecyl), and the extraction efficiency of each sorbent phase was investigated. The sorbent phase was synthesized and characterized by transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), N2 sorption analysis (Brunauer–Emmett–Teller), and thermogravimetric analysis (TGA). The optimized extraction conditions consisted of using 2 mg of the sorbent SBA-15/C8, 2 mL of sample, 2 min of vortex, 4 min of stirring in orbital shaker and 1 min of centrifugation; the desorption step was performed with 25 µL of ACN:acetone (50:50 v/v), vortex for 2 min, 8 min of stirring in orbital shaker and 3 min of centrifugation. The proposed method was validated, with determination coefficients higher than 0.99 for all analytes; LODs and LOQs ranged from 0.15 to 3.03 μg L−1 and from 0.5 to 10.0 μg L−1, respectively; intraday precision ranged from 2.6 to 12.1%; interday precision varied from 4.5 to 25.3%; and accuracy ranged from 92.0 to 112.3 %. This methodology was successfully applied for the analysis of eight groundwater samples from monitoring wells of gas stations in São Paulo. Moreover, according to AGREEprep metrics, the proposed method can be considered sustainable according to the concepts of green analytical chemistry.

Abstract Image

基于硅基纳米结构吸附相的分散微固相萃取-气相色谱-质谱联用技术高效分析多环芳烃
本研究首次以SBA-15介孔二氧化硅为吸附相,提取并测定了环境水样中的10种多环芳烃。提取步骤通过分散-µ-固相萃取(D-µ-SPE)进行,然后进行气相色谱-质谱联用(GC-MS)。特别是,SBA-15的表面与不同的官能团(氨基丙基、苯基、辛基和十八烷基)化学键合,并研究了每个吸附相的萃取效率。合成了吸附剂相,并通过透射电子显微镜(TEM)、傅立叶变换红外光谱(FTIR)、N2吸附分析(Brunauer–Emmett–Teller)和热重分析(TGA)对其进行了表征。优化的提取条件包括使用2 mg吸附剂SBA-15/C8、2 mL样品、2分钟涡流、4分钟在轨道振荡器中搅拌和1分钟离心;解吸步骤用25µL ACN:丙酮(50:50v/v)进行,涡旋2分钟,在轨道振荡器中搅拌8分钟,离心3分钟。所提出的方法得到了验证,所有分析物的测定系数均高于0.99;LOD和LOQ分别为0.15至3.03μg L−1和0.5至10.0μg L–1;日内精密度在2.6%至12.1%之间;日间精密度在4.5%至25.3%之间;准确率为92.0~112.3%。该方法已成功应用于分析圣保罗加油站监测井的8个地下水样本。此外,根据AGREEprep指标,根据绿色分析化学的概念,所提出的方法可以被认为是可持续的。
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CiteScore
3.50
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