Drage Daniel Simon, Sharkey Martin, Berresheim Harald, Coggins Marie, Harrad Stuart
School of Geography, Earth & Environmental Sciences, University of Birmingham, Birmingham B15 2TT, UK.
Queensland Alliance for Environmental Health Sciences (QAEHS), The University of Queensland, 20 Cornwall Street, Woolloongabba, QLD 4103, Australia.
Toxics. 2023 Jan 6;11(1):55. doi: 10.3390/toxics11010055.
Due to new European legislation, products entering the waste stream containing some perfluoro alkyl substances (PFAS) are subject to "low persistent organic pollutant concentration limits". Concentrations of restricted PFAS must be below this limit for them to be legally recycled or disposed of. A rapid extraction and clean-up method was developed for the determination of 21 PFAS in various polymers used in soft furnishings and upholstery. The optimised method used vortexing and ultrasonication in methanol (0.1% NHOH), followed by a dilution and syringe filter clean-up step. PFAS were subsequently determined via UPLC-TripleTOF/MS. Good recoveries (80-120%) of target analytes were obtained with tall and narrow chromatogram peaks. The method was validated using control matrix samples spiked with target analytes. Repeated measurements of concentrations of target compounds showed good agreement with the spiked concentrations demonstrating good accuracy and precision. The resultant extracts provided low noise levels resulting in low limits of quantification ranging from 0.1 to 0.4 mg/kg. The developed method was applied successfully to real consumer products and it provided various advantages over traditional methods, including a substantially reduced analysis time, consumables and solvent consumption, and a high sample throughput which is critical to comply with implemented and proposed legislation.
由于新的欧洲法规,进入废物流的含有某些全氟烷基物质(PFAS)的产品须符合“低持久性有机污染物浓度限值”。受限PFAS的浓度必须低于此限值,才能合法回收或处置。开发了一种快速萃取和净化方法,用于测定软家具和室内装潢中使用的各种聚合物中的21种PFAS。优化后的方法是在甲醇(0.1% NHOH)中进行涡旋和超声处理,随后进行稀释和注射器过滤净化步骤。随后通过超高效液相色谱-三重四极杆飞行时间质谱联用仪(UPLC-TripleTOF/MS)测定PFAS。目标分析物的回收率良好(80-120%),色谱峰高且窄。该方法使用添加了目标分析物的对照基质样品进行了验证。对目标化合物浓度的重复测量结果与加标浓度显示出良好的一致性,表明具有良好的准确度和精密度。所得提取物的噪声水平较低,定量限范围为0.1至0.4 mg/kg。所开发的方法成功应用于实际消费品,与传统方法相比具有多种优势,包括大幅缩短分析时间、减少耗材和溶剂消耗,以及高样品通量,这对于遵守已实施和拟议的法规至关重要。