Department of Soil and Water Conservation and Organic Waste Management, Centro de Edafología y Biología Aplicada del Segura, CSIC, PO Box 4195, 30080 Murcia, Spain; Department of Soil Science, Federal University of Lavras, Department of Soil Science , PO Box 3037, 37200-000 Lavras, Minas Gerais, Brazil.
Chemosphere. 2013 Nov;93(10):2311-8. doi: 10.1016/j.chemosphere.2013.08.023. Epub 2013 Sep 10.
Solid phase microextraction (SPME) is a fast, cheap and solvent free methodology widely used for environmental analysis. A SPME methodology has been optimized for the analysis of VOCs in a range of matrices covering different soils of varying textures, organic matrices from manures and composts from different origins, and biochars. The performance of the technique was compared for the different matrices spiked with a multicomponent VOC mixture, selected to cover different VOC groups of environmental relevance (ketone, terpene, alcohol, aliphatic hydrocarbons and alkylbenzenes). VOC recovery was dependent on the nature itself of the VOC and the matrix characteristics. The SPME analysis of non-polar compounds, such as alkylbenzenes, terpenes and aliphatic hydrocarbons, was markedly affected by the type of matrix as a consequence of the competition for the adsorption sites in the SPME fiber. These non-polar compounds were strongly retained in the biochar surfaces limiting the use of SPME for this type of matrices. However, this adsorption capacity was not evident when biochar had undergone a weathering/aging process through composting. Polar compounds (alcohol and ketone) showed a similar behavior in all matrices, as a consequence of the hydrophilic characteristics, affected by water content in the matrix. SPME showed a good performance for soils and organic matrices especially for non-polar compounds, achieving a limit of detection (LD) and limit of quantification (LQ) of 0.02 and 0.03 ng g(-1) for non-polar compounds and poor extraction for more hydrophilic and polar compounds (LD and LQ higher 310 and 490 ng g(-1)). The characteristics of the matrix, especially pH and organic matter, had a marked impact on SPME, due to the competition of the analytes for active sites in the fiber, but VOC biodegradation should not be discarded in matrices with active microbial biomass.
固相微萃取(SPME)是一种快速、廉价且无需溶剂的方法,广泛应用于环境分析。已经优化了一种 SPME 方法,用于分析不同质地的土壤、不同来源的粪便和堆肥中的有机基质以及生物炭中的挥发性有机化合物(VOC)。该技术的性能已在不同基质中进行了比较,这些基质中加入了一种多组分 VOC 混合物,以涵盖环境相关的不同 VOC 组(酮、萜烯、醇、脂肪族烃和烷基苯)。VOC 的回收取决于 VOC 的性质和基质的特性。SPME 对非极性化合物(如烷基苯、萜烯和脂肪族烃)的分析受到基质类型的显著影响,这是由于 SPME 纤维中的吸附位点竞争所致。这些非极性化合物在生物炭表面上强烈保留,限制了 SPME 在这种类型的基质中的使用。然而,当生物炭通过堆肥经历风化/老化过程时,这种吸附能力就不明显了。极性化合物(醇和酮)在所有基质中表现出相似的行为,这是由于亲水性特征,受基质中水分含量的影响。SPME 对土壤和有机基质表现出良好的性能,特别是对非极性化合物,实现了非极性化合物的检测限(LD)和定量限(LQ)分别为 0.02 和 0.03 ng g(-1),而对更亲水和极性化合物的提取效果较差(LD 和 LQ 分别高于 310 和 490 ng g(-1))。基质的特性,特别是 pH 值和有机物,对 SPME 有显著影响,这是由于分析物在纤维中的活性位点竞争所致,但在具有活性微生物生物量的基质中,不应排除 VOC 生物降解的可能性。