ASTM: D6592:  Water Quality by Chemiluminesence

  • Summary
  • Analytes
  • Revision
  • Data and Sites
Official Method Name
Standard Test Method for Portable Chemiluminescent Water Quality Determination
Current Revision
Current edition approved March 10, 2001. Published May 2001.
Media
WATER
Instrumentation
Portable Luminometer
Method Subcategory
Organic
Method Source
  ASTM
Citation
  Annual Book of ASTM Standards, Section 11, Water and Environmental Technology, Volume 11.02, Water (I)
Brief Method Summary
This analytical test method is an enhanced chemiluminescent method based on the procedure of Whitehead et al. Luminol is oxidized by a complex formed between an oxidant and peroxidase (HRP) to form a luminol radical. This decomposes via an endoperoxide intermediate to form the excited state 3-aminophthalate dianion which decays to its ground state with the emission of light. The presence of enhancers results in a steady output of luminol radicals during the reaction (see Fig. 1 in the method). Contaminating substances (such as sewage, silage effluent, heavy metals, detergents, cyanides and pesticides containing organic residues) react with the assay reagents by scavenging radicals from the luminol or enhancer radicals, or by inhibiting the catalytic action of HRP. This results in a reduction of light output to a degree which is proportional to the amount of contaminant present. Light output is measured using a portable luminometer, which detects light by means of a silicon photodiode.
Scope and Application
This test method covers the detection of water and wastewater contaminants which inhibit chemiluminescence. This test method may be applied to ambient waters including but not exclusively river water and water from sewage treatment plants. It is the responsibility of the user of this standard to ensure the validity of the test method for waters of untested matrices.
Applicable Concentration Range
0-100 %
Interferences
Particulate Matter - Samples containing a high degree of particulate matter can interfere with the test. Particulate or suspended matter may be removed by centrifugation or membrane filtration if components of interest are not altered.
Quality Control Requirements
Before this test method is applied to the analysis of samples, the analyst must establish quality control by the procedures recommended in Practice D 4210 and Guide D 3856.
Quality control (QC) requirements are the initial demonstration of laboratory capability followed by regular analyses of quality control standard material. Other criteria may be more appropriate in a given situation depending on the data quality objectives.
Sample Handling
Collect all samples in accordance with Specification D 1192 and Practice D 3370, as applicable.
Samples must be collected in glass or plastic containers that are clean and flee from artifacts and or interferences. The suitability of the containers should be demonstrated for each new lot by performing a container blank.
Preserve samples by cooling to 4oC for up to 24 h after sampling. If it is necessary to hold samples for longer than 24 hours, it is the responsibility of the user of the test to determine the maximum holding time for individual samples.
Maximum Holding Time
24 hours
Relative Cost
Less than $50
Sample Preparation Methods