EPA-RCA: 8091 (by GC-NPD):  Nitroaromatics and Cyclic Ketones in Water, Soil, and Waste by GC-NPD

  • Summary
  • Analytes
  • Revision
  • Data and Sites
Official Method Name
Nitroaromatics and Cyclic Ketones by Gas Chromatography
Current Revision
Revision 0, December 1996
Media
VARIOUS
Instrumentation
Gas Chromatography with Nitrogen - Phosphorus Detection
Method Subcategory
Organic
Method Source
  EPA-RCA
Citation
  SW-846 Online: Test Methods for Evaluating Solid Waste, Physical/Chemical Methods
Brief Method Summary
Samples are extracted and cleaned up (according to sample matrix) and then are directly injected into a gas chromatograph to be analyzed by wide bore capillary columns with either an electron capture detector or nitrogen-phosphorous detector.
Scope and Application
This method determines the concentration of nitroaromatics and cyclic ketones in water, soil, and waste matrices by using wide-bore, open-tubular, capillary column gas chromatography with either electron capture detection or nitrogen-phosphorus detection.
Applicable Concentration Range
Not Available.
Interferences
(A) Memory Interferences: Carryover may occur whenever high and low concentration samples are analyzed in sequence. For prevention, rinse the sample syringe between samples with solvent. Also, unusually concentrated samples should be followed by the analysis of a solvent blank. Additional solvent blanks interspersed with the sample extracts should be analyzed whenever a solvent blank indicates cross-contamination.
(B) Coeluting Compounds: Some compounds coelute on either one or both columns, in which case, they must be reported as coeluting. The samples may be reanalyzed by GC/MS.
(C) Electronegative Compound Interferences: Interferences may be caused by halogenated compounds, phthalates, and other oxygenated compounds, in which case, second column or GC/MS confirmation is necessary to ensure proper analyte identification.
Quality Control Requirements
Refer to Chapter One and Methods 8000, 3500, and 5000 for specific QC procedures. Procedures include: validation of sample preparation, introduction, and analysis, initial demonstration of proficiency, calibration verification, evaluation of retention times, analysis of method blanks, matrix spikes, duplicates, surrogates, and laboratory control samples.
Sample Handling
See the introductory material to this chapter, "Organic Analytes", Section 4.1. Extracts must be stored in the dark at or below 4oC.
Maximum Holding Time
40 days.
Relative Cost
$201 to $400
Sample Preparation Methods
3500, 3510, 3520, 3600, 3620, 3640, 3660