EPA-EAD: 1640:  Trace Elements in Ambient Waters by On-Line Chelation

  • Summary
  • Analytes
  • Revision
  • Data and Sites
Official Method Name
Determination of Trace Elements in Ambient Waters by On-Line Chelation Preconcentration and Inductively Coupled Plasma-Mass Spectrometry
Current Revision
April 1997
Media
WATER
Instrumentation
Inductively Coupled Plasma - Mass Spectrometry
Method Subcategory
Inorganic
Method Source
  EPA-EAD
Citation
  EPA Method Guidance CD-ROM (includes MCAWW Methods, and most current EPA Methods)
Brief Method Summary
A sample is acidified and solubilized by gentle refluxing (if total recoverable elements are desired). Elements in a sample are preconcentrated using an iminodiacetate functionalized chelating resin. Group I and II metals, as well as most anions, are selectively separated from the analytes by elution with ammonium acetate at pH 5.5. The elements are subsequently eluted into a simplified matrix consisting of dilute nitric acid and are determined by ICP-MS using a directly coupled on-line configuration.
Scope and Application
This method determines dissolved elements in ambient waters at EPA water quality criteria (WQC) levels. It may also be used for determination of total recoverable element concentrations in these waters.
Applicable Concentration Range
Not Available.
Interferences
(A) Contamination by carryover.
(B) Contamination of apparatus by direct and indirect contact.
(C) Contamination by airborne particulate matter.
(D) Isobaric elemental interferences.
(E) Wing overlap of m/z peaks.
(F) Isobaric polyatomic ion interferences of similar m/z's
(G) Physical interferences.
(H) Competing chelators.
Quality Control Requirements
The minimum requirements consist of an initial demonstration of laboratory capability, analysis of samples spiked with metals of interest to evaluate and document data quality, and analysis of standards and blanks as tests of continued performance.
Sample Handling
Collect samples as described in EPA Method 1669. For dissolved metals, samples and field blanks are filtered through a 0.45 um capsule filter at the field site. Preservation of samples and field blanks for both dissolved and total recoverable elements may be performed in the field when the samples are collected or in the laboratory. Preservation involves the addition of 10% HNO3 to bring the sample to pH < 2. For samples received at neutral pH, approximately 5 mL of 10% HNO3 per liter will be required. Store preserved sample for a minimum of 48 hours at 0-4oC. Sample bottles should be stored in polyethylene bags at 0-4oC until analysis.
Maximum Holding Time
6 months (after preservation)
Relative Cost
$51 to $200
Sample Preparation Methods
None.