On-line and in-situ detection of lead aerosols by plasma-spectroscopy and laser-excited atomic fluorescence spectroscopy

被引:96
作者
Neuhauser, RE
Panne, U
Niessner, R
Petrucci, GA
Cavalli, P
Omenetto, N
机构
[1] UNIV MUNICH,INST HYDROCHEM,D-81377 MUNICH,GERMANY
[2] COMMISS EUROPEAN COMMUNITIES,JOINT RES CTR,INST ENVIRONM,I-21020 ISPRA,VARESE,ITALY
关键词
ultrafine aerosols; lead; laser-induced plasma; LIBS; laser excited atomic fluorescence; LEAF; plasma spectroscopy;
D O I
10.1016/S0003-2670(97)00244-4
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A set-up for on-line and size-segregated detection of lead in ultrafine aerosols was developed. Lead nitrate aerosols with particle diameters between 10 and 300 nm were generated by ultrasonic nebulization of aqueous PbO(NO3)(2)-solutions. A differential mobility particle sizer (DMPS) was used for size-resolved mass calibration. Either a miniaturized acetylene-air-flame or a laser-induced plasma (LIP) was employed for atomization. Lead was detected with a spectrograph and a gateable, intensified CCD-camera by atomic emission spectroscopy (AES) and laser excited atomic fluorescence (LEAF). Due to the lower sensitivity, for LIP-AES no size-resolved calibration was possible and for calibration with polydisperse aerosols a detection limit of 155 mu g m(-3) was found for lead. With LEAF and flame atomization, a linear calibration curve was obtained with on-line detection limits of 47 ng m(-3) for lead. No dependence of the detection limit on the particle diameter was observed. For LEAF with a laser-induced plasma as atom source, a correlation between the detection limit and the particle diameter was found. The detection limit increased from 55 ng m(-3) for a particle diameter of 48 nm to 130 ng m(-3) for a particle diameter of 300 nm. The increasing detection limit with increasing particle diameter was probably due to the incomplete atomization of larger particles in the colder periphery of the plasma.
引用
收藏
页码:37 / 48
页数:12
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