EPA: 8318 A:  N-methylcarbamates in soil, water, and waste matrices by high performance liquid chromatography (HPLC)

  • Summary
  • Analytes
  • Revision
  • Data and Sites
Official Method Name
EPA Method 8318A: N-methylcarbamates by high performance liquid chromatography (HPLC)
Current Revision
Revision 1, February 2007
Media
VARIOUS
Instrumentation
High Performance Chromatography with Post Column Derivitization and Fluorescence Detection
Method Subcategory
Organic
Method Source
  EPA
Citation
  SW-846 Online: Test Methods for Evaluating Solid Waste, Physical/Chemical Methods
Brief Method Summary
N-methylcarbamates are extracted from samples using various 3500 series extraction methods, or other methods that are appropriate for the sample matrix. Extracts may be subjected to an optional cleanup procedure designed to remove interferences. During cleanup, the solvent is exchanged to methanol for analysis. Extracts are analyzed by HPLC, on a C-18 reversed-phase column. After separation, the target analytes are hydrolyzed and derivatized post-column, then quantitated.
Scope and Application
This method covers the determination of N-methylcarbamates in soil, water, and waste matrices
Applicable Concentration Range
Not given
Interferences
(A) Solvents, reagents, glassware, and other sample processing hardware contamination: Analyze method blanks, distill reagents and solvents in all-glass systems if necessary. (B) Fluorescent compounds, primarily alkyl amines and compounds which yield primary alkyl amines upon base hydrolysis: No remedy. (C) Coeluting compounds that are fluorescence quenchers may result in negative interferences: No remedy. (D) Also refer to Methods 3500 and 8000.
Quality Control Requirements
Mixed QC standard, method blank, laboratory control sample (LCS), (optional) surrogates, matrix spike, and matrix spike duplicate, solvent blank, clean refence matrix, calibration verification standards,
Sample Handling
Preserve immediately (acidify to pH 4-5 with 0.1 N chloroacetic acid). Store samples at 6 ˚C out of direct sunlight from the time of collection through analysis.
Maximum Holding Time
7 days for extraction after collection, 40 days for analysis after extraction
Relative Cost
Sample Preparation Methods
Various 3500 series extraction methods, other methods, some of which given here.