Chemical Mechanism and Efficiency of the Sulfur Chemiluminescence Detector

1994 ◽  
Vol 48 (7) ◽  
pp. 848-851 ◽  
Author(s):  
Richard L. Benner ◽  
Donald H. Stedman

The sulfur chemiluminescence detector (SCD) is a sensitive, highly selective sulfur detection system based on reaction in hydrogen/air combustion followed by extraction and low-pressure chemiluminescence. This report documents investigations into the fundamental chemical processes occurring in the SCD. The conclusion from this work is that ozone reacts with sulfur monoxide (SO) to form electronically excited SO2. A gas-phase titration of the SO formed indicates that approximately four of every 1000 sulfur-containing molecules entering the flame arrive at the reaction cell as SO. This new understanding of the SCD will allow future studies to concentrate on optimization of instrumental performance based on the appropriate chemical mechanism.

1992 ◽  
Vol 46 (6) ◽  
pp. 948-952 ◽  
Author(s):  
Harold R. Martin ◽  
Robert J. Glinski

Gases from a hydrogen-rich, sulfur-dioxide-containing, hydrogen/oxygen flame were drawn into a reduced-pressure reaction vessel and reacted with ozone. Spectroscopic analysis of the low-pressure chemiluminescence showed that electronically excited sulfur dioxide is the principal emitter exploited in the new sulfur chemiluminescence detector (SCD). Sulfur dioxide phosphorescence was found to contribute significantly to the total emission, suggesting that the technique could be enhanced by detecting more of the phosphorescence at higher total pressures. A calibration plot of signal vs. sulfur dioxide concentration was found to have a slight positive curvature. Interferences from NO2* and OH* were spectroscopically characterized; it is suggested that these could be minimized in the SCD by judicious choice of the wavelength discrimination filter. Utilization of a microwave discharge was similarly efficient at producing the chemiluminescence.


Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2768 ◽  
Author(s):  
Sergei V. Makarov ◽  
Attila K. Horváth ◽  
Anna S. Makarova

Oxidation of sulfide to sulfate is known to consist of several steps. Key intermediates in this process are the so-called small oxoacids of sulfur (SOS)—sulfenic HSOH (hydrogen thioperoxide, oxadisulfane, or sulfur hydride hydroxide) and sulfoxylic S(OH)2 acids. Sulfur monoxide can be considered as a dehydrated form of sulfoxylic acid. Although all of these species play an important role in atmospheric chemistry and in organic synthesis, and are also invoked in biochemical processes, they are quite unstable compounds so much so that their physical and chemical properties are still subject to intense studies. It is well-established that sulfoxylic acid has very strong reducing properties, while sulfenic acid is capable of both oxidizing and reducing various substrates. Here, in this review, the mechanisms of sulfide oxidation as well as data on the structure and reactivity of small sulfur-containing oxoacids, sulfur monoxide, and its precursors are discussed.


1999 ◽  
Vol 33 (4) ◽  
pp. 625-632 ◽  
Author(s):  
Douglas L. MacTaggart ◽  
Sherry O. Farwell ◽  
Julia R. Burdge ◽  
Zhong-Tao Cai ◽  
Timothy J. Haakenson ◽  
...  

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