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.
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页码:37 / 48
页数:12
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