4.7 Article

Optimization and evaluation of multi-bed adsorbent tube method in collection of volatile organic compounds

Journal

ATMOSPHERIC RESEARCH
Volume 202, Issue -, Pages 187-195

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.atmosres.2017.11.026

Keywords

VOCs; Method optimization; Thermal desorption; Adsorbent tube; Ozone precursor

Funding

  1. National Key Research and Development Program of China [2016YFA0203000]
  2. National Science Foundation of China [41401567, 41503117, 41573138]
  3. Chinese Academy of Sciences [XDB05000000]
  4. Chinese Academy of Sciences

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The feasibility of using adsorbent tubes to collect volatile organic compounds (VOCs) has been demonstrated since the 1990's and standardized as Compendium Method TO-17 by the U.S. Environmental Protection Agency (U.S EPA). This paper investigates sampling and analytical variables on concentrations of 57 ozone (O-3) precursors (C-2-C-12 aliphatic and aromatic VOCs) specified for the Photochemical Assessment Monitoring Station (PAMS). Laboratory and field tests examined multi-bed adsorbent tubes containing a sorbate combination of Tenax TA, Carbograph 1 TD, and Carboxen 1003. Analyte stabilities were influenced by both collection tube temperature and ambient O-3 concentrations. Analytes degraded during storage, while blank levels were elevated by passive adsorption. Adsorbent tube storage under cold temperatures (- 10 degrees C) in a preservation container filled with solid silica gel and anhydrous calcium sulfate (CaSO4) ensured sample integrity. A high efficiency (> 99%) O-3 scrubber (i.e., copper coil tube filled with saturated potassium iodide [KM removed O-3 (i.e., < 200 ppbv) from the air stream with a sampling capacity of 30 h. Water vapor scrubbers interfered with VOC measurements. The optimal thermal desorption-gas chromatography/mass spectrometry (TD-GC/MS) desorption time of 8 min was found at 330 degrees C. Good linearity (R-2 > 0.995) was achieved for individual analyte calibrations (with the exception of acetylene) for mixing ratios of 0.08-1.96 ppbv. The method detection limits (MDLs) were below 0.055 ppbv for a 3 L sample volume. Replicate analyses showed relative standard deviations (RSDs) of < 10%, with the majority of the analytes within < 5%.

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