Sakurai Kenji, Eba Hiromi, Inoue Katsuaki, Yagi Naoto
National Institute for Materials Science, Tsukuba, Ibaraki, Japan.
Anal Chem. 2002 Sep 1;74(17):4532-5. doi: 10.1021/ac025720y.
The present paper reports significant enhancement of the detection power for total-reflection X-ray fluorescence (TXRF). The employment of an efficient wavelength-dispersive spectrometer rather than a conventional Si(Li) detector, as well as the use of a quasi-monochromatic undulator X-ray source, completely changed the quality of X-ray florescence spectra. The energy resolution is 20 times better, which effectively contributes to reducing the low-energy tail of the scattering background and to separating neighboring X-ray florescence peaks. Another advantage is its capability with respect to high-counting-rate measurements, which ensure the detection of weak signals from trace materials. The absolute and relative detection limit for nickel are 3.1 x 10(-16) g and 3.1 ppt (pg/g) for a 0.1-microL droplet of pure water, respectively, which is nearly 50 times better than the current best data achieved by conventional energy-dispersive TXRF using a Si(Li) detector system.
本文报道了全反射X射线荧光光谱法(TXRF)检测能力的显著提高。采用高效的波长色散光谱仪而非传统的Si(Li)探测器,以及使用准单色波荡器X射线源,彻底改变了X射线荧光光谱的质量。能量分辨率提高了20倍,这有效地减少了散射背景的低能尾部,并有助于分离相邻的X射线荧光峰。另一个优点是它能够进行高计数率测量,从而确保检测到痕量物质的微弱信号。对于0.1微升的纯水液滴,镍的绝对检测限和相对检测限分别为3.1×10(-16)克和3.1 ppt(皮克/克),这比使用Si(Li)探测器系统的传统能量色散TXRF目前获得的最佳数据要好近50倍。