Sensor-triggered sampling to determine instantaneous airborne vapor exposure concentrations.

It is difficult to measure transient airborne exposure peaks by means of integrated sampling for organic chemical vapors, even with very short-duration sampling. Selection of an appropriate time to measure an exposure peak through integrated sampling is problematic, and short-duration time-weighted...

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Publicado en:Journal of Occupational & Environmental Hygiene Vol. 15; no. 6; pp. 510 - 518
Autores principales: Smith, Philip A., Simmons, Michael K., Toone, Phillip
Formato: research tables/charts Journal Article
Publicado: Taylor & Francis Ltd Jun2018
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jun2018
      vid: 15
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      pub: Taylor & Francis Ltd
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        10.1080/15459624.2018.1453141
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        atl: Sensor-triggered sampling to determine instantaneous airborne vapor exposure concentrations.
      aug:
        au:
          Smith, Philip A.
          Simmons, Michael K.
          Toone, Phillip
        affil: U.S. Department of Labor - OSHA, Directorate of Technical Support and Emergency Management, Salt Lake Technical Center, Industrial Hygiene Chemistry Division, Sandy, Utah
      sug:
        subj:
          Environmental Exposure
          Toluene Analysis
          Hydrocarbons, Chlorinated Analysis
          Human
          Gas Chromatography-Mass Spectrometry
          Humidity
          Trigger Point
          Precision
          Calibration
          Confidence
          Reliability
          Laboratories
      ab: It is difficult to measure transient airborne exposure peaks by means of integrated sampling for organic chemical vapors, even with very short-duration sampling. Selection of an appropriate time to measure an exposure peak through integrated sampling is problematic, and short-duration time-weighted average (TWA) values obtained with integrated sampling are not likely to accurately determine actual peak concentrations attained when concentrations fluctuate rapidly. Laboratory analysis for integrated exposure samples is preferred from a certainty standpoint over results derived in the field from a sensor, as a sensor user typically must overcome specificity issues and a number of potential interfering factors to obtain similarly reliable data. However, sensors are currently needed to measure intra-exposure period concentration variations (i.e., exposure peaks). In this article, the digitized signal from a photoionization detector (PID) sensor triggered collection of whole-air samples when toluene or trichloroethylene vapors attained pre-determined levels in a laboratory atmosphere generation system. Analysis by gas chromatography-mass spectrometry of whole-air samples (with both 37 and 80% relative humidity) collected using the triggering mechanism with rapidly increasing vapor concentrations showed good agreement with the triggering set point values. Whole-air samples (80% relative humidity) in canisters demonstrated acceptable 17-day storage recoveries, and acceptable precision and bias were obtained. The ability to determine exceedance of a ceiling or peak exposure standard by laboratory analysis of an instantaneously collected sample, and to simultaneously provide a calibration point to verify the correct operation of a sensor was demonstrated. This latter detail may increase the confidence in reliability of sensor data obtained across an entire exposure period.
      pubtype: Academic Journal
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      ougenre: Article
    language: English
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