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TRICHLOROETHYLENE: METHOD 1022, Issue 2, dated 15 August 1994 - Page 3 of 4 9.

10.

Determine desorption efficiency (DE) at least once for each lot of sorbent used for sampling in the range of interest. Prepare three tubes at each of five concentrations plus three media blanks. a. Remove and discard back sorbent section of a media blank sampler. b. Inject a known amount (2 to 20 µL) of TCE, or a standard solution thereof in CS 2, directly onto front sorbent section with a microliter syringe. c. Cap the tube. Allow to stand overnight. d. Desorb (steps 5 through 7) and analyze with working standards (steps 11 and 12). e. Prepare a graph of DE vs. mg TCE recovered. Analyze three quality control blind spikes and three analyst spikes to ensure that the calibration graph and DE graph are in control.

MEASUREMENT: 11.

12.

Set gas chromatograph according to manufacturer's recommendations and to conditions given on page 1022-1. Inject sample aliquot manually using solvent flush technique or with autosampler. NOTE: If peak area is above the linear range of the working standards, dilute an aliquot of the desorbed liquid with CS 2, reanalyze, and apply the appropriate dilution factor in calculations. Measure peak area.

CALCULATIONS: 13.

14.

Determine the mass, mg (corrected for DE) of TCE found in the sample front (W f) and back (W b) sorbent sections and in the average media blank front (B f) and back (B b) sorbent sections. NOTE: If W b > W f/10, report breakthrough and possible sample loss. Calculate concentration, C, of TCE in the air volume sampled, V (L):

EVALUATION OF METHOD: Method S336 was issued on June 6, 1975 [4], and validated with generated atmospheres using a calibrated syringe drive [1]. Average recoveries were 92 to 94% (16 samples) in the range 477 to 2025 mg/m 3 for 3.4-L samples. Breakthrough volume of 18.5 L (effluent = 5% of test concentration) occurred after sampling for 99 min at 0.187 L/min from an atmosphere containing 2266 mg/m 3 trichloroethylene in dry air. Desorption efficiency for SKC Lot 105 activated coconut charcoal in the range 1.6 to 6.4 mg per sample averaged 96.4% with Sr = 0.7% (18 samples). n-Octane was used as an internal standard in the chromatographic measurements. The semi-quartile ranges of desorption efficiencies in two rounds of the Proficiency Analytical Testing (PAT) program were 0.97 to 1.0 for charcoal tubes spiked with 0.6 to 1.1 mg trichloroethylene [9].

REFERENCES: [1]

[2] [3]

Documentation of the NIOSH Validation Tests, S336, U.S. Department of Health, Education, and Welfare, Publ. (NIOSH) 77-185 (1977), available at Stock No. PB 274-248 from NTIS, Springfield, VA 22161. UBTL Report for NIOSH Sequence #4266-R (NIOSH, unpublished, March 26, 1984). UBTL Report for NIOSH Sequence #4266-N (NIOSH, unpublished, March 14, 1984).

NIOSH Manual of Analytical Methods (NMAM), Fourth Edition, 8/15/94