Manera Matías, Miró Manuel, Estela José Manuel, Cerdà Víctor
Department of Chemistry, Faculty of Sciences, University of the Balearic Islands, Carretera de Valldemossa Km.7.5, E-07122 Palma de Mallorca, Spain.
Anal Chim Acta. 2007 Jan 16;582(1):41-9. doi: 10.1016/j.aca.2006.08.063. Epub 2006 Sep 12.
In this paper, a time-based multi-syringe flow injection (MSFI) approach is proposed for automated disk-based sorbent extraction of three nitro-substituted phenol isomers (2-, 3-, and 4-nitrophenol) followed by on-line simultaneous determination of individual species by diode-array spectrophotometry. The method involves the on-line enrichment of the targeted analytes from an acidic medium containing 0.1 mol L(-1) HCl onto a co-polymeric sorbent material, and the concurrent removal of potentially interfering matrix components. The nitrophenol isomers are subsequently eluted with an alkaline solution (0.7 mol L(-1) NaOH), whereupon the eluate is delivered to a diode-array spectrophotometer for recording of the spectral data in the UV-vis region. Deconvolution of strongly overlapped spectra was conducted with multivariate regression models based on multiple linear regression calibration. The analytical performance of the chemometric algorithm was characterized by relative prediction errors and recoveries. The MSFI manifold was coupled to a multiposition selection valve to set a rugged analyzer that ensures minimum operational maintenance via exploitation of membrane switching protocols. As compared with earlier methods for isolation/pre-concentration of nitro-substituted phenols based on liquid-liquid extraction, the proposed flow-through disk-based system should be regarded as an environmentally friendly approach because the use of harmful organic solvents is circumvented. Under the optimized chemical and physical variables, the 3sigma(blank) detection limits for 2-, 3-, and 4-nitrophenol were 1.2, 3.2 and 0.3 micromol L(-1) for a sample loading volume of 1.5 mL, and the relative standard deviations were < or =5.0%. The flowing system, which is able to handle up to 135 samples automatically, was proven suitable for monitoring trace levels of the target isomers in mineral, tap, and seawater.
本文提出了一种基于时间的多注射器流动注射(MSFI)方法,用于对三种硝基取代酚异构体(2-、3-和4-硝基苯酚)进行基于盘的吸附剂自动萃取,随后通过二极管阵列分光光度法在线同时测定各组分。该方法包括将目标分析物从含有0.1 mol L⁻¹ HCl的酸性介质中在线富集到共聚吸附剂材料上,并同时去除潜在干扰的基质成分。硝基苯酚异构体随后用碱性溶液(0.7 mol L⁻¹ NaOH)洗脱,然后将洗脱液输送到二极管阵列分光光度计中,用于记录紫外-可见区域的光谱数据。基于多元线性回归校准的多元回归模型对严重重叠的光谱进行了去卷积处理。化学计量算法的分析性能通过相对预测误差和回收率来表征。MSFI流路与多位置选择阀相连,以设置一种坚固耐用的分析仪,通过利用膜切换协议确保最低的操作维护。与早期基于液-液萃取的硝基取代酚分离/预浓缩方法相比,所提出的基于盘的流通系统应被视为一种环保方法,因为避免了使用有害有机溶剂。在优化的化学和物理变量下,对于1.5 mL的进样体积,2-、3-和4-硝基苯酚的3σ(空白)检测限分别为1.2、3.2和0.3 μmol L⁻¹,相对标准偏差≤5.0%。该流动系统能够自动处理多达135个样品,已被证明适用于监测矿物水、自来水和海水中痕量水平的目标异构体。