We present a kinetic study of the reaction of ground state silicon atoms with halogenated unsaturated organic compounds (R). Si(33PJ) was generated by the repetitive pulsed irradiation of SiC1, in the presence of excess helium buffer gas and the reactant R in a slow flow system, kinetically equivale
Time-resolved spectroscopy of long-path fluorescence and scattering for measuring total absorption of fluids
โ Scribed by K.-H. Mittenzwey; G. Sinn
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 468 KB
- Volume
- 330
- Category
- Article
- ISSN
- 0003-2670
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โฆ Synopsis
Optical methods are appropriate tools to detect organic micro-pollutants in fluids. A new technique is introduced which uses the decay of interaction processes like fluorescence and elastically scattered radiation by a fluid. Principally two different parameters are determined: (i) the decay-time of the conventional interaction ro, which occurs at relatively short path-lengths of the incidence beam in the fluid, and (ii) the decay-time rMp of the multi-path-saturation interaction originating at long pathlengths, e.g. in multi-path-reflection cuvettes, where the incidence beam is fully absorbed by the fluid. A relation between the decay-time and the absorption coefficient of a fluid is theoretically derived. A simple preliminary experiment is performed considering distilled water polluted with non-fluorescent azobenzene and fluorescent quinine-sulphate. A nitrogen laser has been used to generate the fluorescence and scattering signals. The reciprocal value of the difference between the decay-time of the multi-path and conventional signals, l/(7 MP-rc), yields the total absorption coefficient directly. In comparison to the conventional absorption technique the decay-time method is characterized by a higher sensitivity.
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We present a kinetic study of atomic potassium in its electronic ground state, K(4'SI 21, generated in the "single-shot mode" by pulsed irradiation at elevated temperatures and monitored by time-resolved atomic resonance absorption spectroscopy using the Rydberg doublet at A = 404 nm (K[5'PJ] +K[42S