A cataluminescence gas sensor based on nanosized V2O5 for tert-butyl mercaptan

被引:39
|
作者
Zhang, Huili [1 ]
Zhang, Lichun [1 ]
Hu, Jing [1 ]
Cai, Pingyang [1 ]
Lv, Yi [1 ]
机构
[1] Sichuan Univ, Key Lab Green Chem & Technol MOE, Coll Chem, Chengdu 610064, Peoples R China
关键词
Cataluminescence; Gas sensor; Vanadium pentoxide; Tert-butyl mercaptan; ORGANIC SULFUR-COMPOUNDS; SOLID-PHASE MICROEXTRACTION; CHEMILUMINESCENCE DETECTOR; THERMAL-DESORPTION; ARRAY; AIR; CHROMATOGRAPHY; MECHANISM; OXIDATION; CATALYSTS;
D O I
10.1016/j.talanta.2010.05.040
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This work proposed a gas sensor for the determination of tert-butyl mercaptan. one of the highly toxic volatile sulfur compounds, which was based on cataluminescence emission during its catalytic oxidation on the surface of nanosized V2O5. The cataluminescence characteristics and the optimum conditions, including the morphology of sensing material, the wavelength of cataluminescence emission, the oxygen flow rate and working temperature were investigated in detail. Under the optimized conditions, the calibration curve of the relative cataluminescence intensity versus the concentration of tert-butyl mercaptan vapor was made, with the linear range of 5.6-196 mu g mL(-1) and the detection limit of 0.5 mu g mL(-1) (S/N = 3). The relative standard deviation (R.S.D.) (n = 5) of relative cataluminescence intensity for 84 mu g mL(-1) tertbutyl mercaptan was 3.6%. There is no or weak response to some common substances, such as formic acid, alcohol (methanol, ethanol, propanol, isopropanol, n-butanol. isoamyl alcohol), o-dichlorobenzene. acetonitrile, ethyl acetate, aldehyde (formaldehyde, acetaldehyde and propanal), 1,2-dichloroethane and ammonia. Furthermore, the proposed sensor was successfully used for determining tert-butyl mercaptan in four artificial samples, with a good recovery. The results demonstrated that the proposed gas sensor had a promising capability for the tert-butyl mercaptan in routine monitoring. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:733 / 738
页数:6
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