Institute of Optics and Atomic Physics, Technical University of Berlin, Germany.
Mar Pollut Bull. 2012 Mar;64(3):614-26. doi: 10.1016/j.marpolbul.2011.12.008. Epub 2012 Jan 16.
A field operable surface enhanced Raman scattering (SERS) sensor system was applied for the first time under real conditions for the detection of polycyclic aromatic hydrocarbons (PAHs) as markers for petroleum hydrocarbons in the Gulf of Gdańsk (Baltic Sea). At six stations, seawater samples were taken, and the sensor system was applied in situ simultaneously. These measurements were compared to the results of conventional GC/MS laboratory analysis of the PAH concentrations in the seawater samples. For a PAH concentration above 150 ng(12PAH)l(-1), there was agreement between the SERS sensor and the GC/MS determinations. A standard addition experiment yielded a PAH concentration of 900 ng l(-1) at the Gdańsk Harbor, which was of the same order as the GC/MS determinations of 12PAHs (200 ng(12PAH)l(-1)). The high SERS detection limit for seawater samples is explained by the competition for PAHs between the sensor membrane and particulate matter surfaces. Thus, the SERS sensor can be applied, e.g., as a non-quantitative alarm sensor for relatively high PAH concentrations in heavily polluted waters. The spectral unmixing procedure applied for Gdańsk Harbor water confirmed the presence of phenanthrene at the highest concentration ([Phe]=140 ngl(-1)) and of Chr (2.7 ng l(-1)), but it did not detect the other PAHs present in the Gdańsk Harbor water, as determined by GC/MS. When compared to the past literature and databases, the SERS spectra indicated the presence of a mixture of molecules consisting of carotenoids, n-alkanes, amines or fatty acids, and benzimidazoles at the coastal station ZN2. The spectra in the offshore direction indicated carboxylic acids. Interpretation of the farthest offshore in situ SERS measurements is difficult, principally due to the limited availability of reference spectra. The detection of the lower PAH concentrations commonly found in Baltic coastal water needs further research and development to obtain better sensitivity of the SERS sensor. However, the high analytical specificity of the SERS sensor also allows the detection of other chemical species that require the development of a SERS/Raman library for specific in situ spectral interpretation.
首次在真实条件下应用现场可操作的表面增强拉曼散射(SERS)传感器系统,用于检测波罗的海格但斯克湾(Gulf of Gdańsk)作为石油烃标志物的多环芳烃(PAHs)。在六个站位采集了海水样本,并同时原位应用传感器系统。这些测量结果与海水样本中 PAH 浓度的常规 GC/MS 实验室分析结果进行了比较。对于浓度高于 150 ng(12PAH)l(-1)的 PAH,SERS 传感器和 GC/MS 测定结果一致。在格但斯克港进行的标准添加实验得出的 PAH 浓度为 900 ng l(-1),与 GC/MS 测定的 12PAHs(200 ng(12PAH)l(-1))浓度相当。海水样本的高 SERS 检测限是由于传感器膜和颗粒物表面之间对 PAHs 的竞争造成的。因此,SERS 传感器可以应用于例如,作为受污染严重水域中相对较高 PAH 浓度的非定量警报传感器。应用于格但斯克港水域的光谱解混程序证实了水中菲的浓度最高([Phe]=140 ngl(-1))和 Chr(2.7 ng l(-1))的存在,但未检测到 GC/MS 测定的格但斯克港水中存在的其他 PAHs。与过去的文献和数据库相比,SERS 光谱表明,在近岸站 ZN2 存在由类胡萝卜素、正烷烃、胺或脂肪酸和苯并咪唑组成的分子混合物。在近海方向的光谱表明存在羧酸。对最偏远的原位 SERS 测量的解释很困难,主要是由于参考光谱的有限可用性。需要进一步的研究和开发来提高 SERS 传感器的灵敏度,以检测波罗的海沿海水中常见的较低 PAH 浓度。然而,SERS 传感器的高分析特异性还允许检测其他需要为特定原位光谱解释开发 SERS/Raman 库的化学物质。