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Water Quality Monitoring Report - Noosa Civic - November 2009-2010 - Eenie Creek Rd NOOSAVILLE · 132002.220285
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Work Order EB1014514
Client DUKE ENVIRONMENTAL
Project DE0923
Brief Method Summaries
The analvti,-A procedures used by the Environmental Division have been developed from established internationally recognized procedures such as those published by the US EPA. APHA, AS and NEW In house
d.-veloped procedures are employed in the absence of documented standards or by client request The following report provides brief descriptions of the analytical procedures employed for results reported in the
Certificate of Analysis. Sources from which ALS methods have been developed are provided within the Method Descriptions.
Suspended Solids (High Level) EA025H WATER APHA 21st ed., 2540D A gravimetric procedure employed to determine the amount of 'non-filterable' residue in a
aqueous sample. The prescribed GFC (1.2um) filter is rinsed with deionised water, oven dried and weighed prior to
analysis A well-mixed sample is filtered through a glass fibre filter (1 2um). The residue on the filter paper is
dried at 104+/-2C . This method is compliant with NEPM (1999) Schedule B(3) (Appdx. 2)
Hardness as CaCO3 EA065 WATER APHA 21st ed., 2340 B. This method is compliant with NEPM (1999) Schedule B(3) (Appdx. 2)
Major Cations - Dissolved ED093F WATER APHA 21st ed., 3120: USEPA SW 846 - 6010 The ICPAES technique ionises the 045um filtered sample atoms
emitting a characteristic spectrum This spectrum is then compared against matrix matched standards for
quantification. This method is compliant with NEPM (1999) Schedule B(3) (Appdx. 2)
Dissolved Metals by ICP-MS - Suite A EG020A-F WATER (APHA 21st ed., 3125; USEPA SW846 - 6020, ALS QWI-EN/EGO20): Samples are 0.45 um filtered prior to
analysis The ICPMS technique utilizes a highly efficient argon plasma to ionize selected elements. Ions are then
passed into a high vacuum mass spectrometer, which separates the analytes based on their distinct mass to
charge ratios prior to their measurement by a discrete dynode ion detector.
Ammonia as N by Discrete analyser EK055G WATER APHA 21st ed., 4500-NH3 G Ammonia is determined by direct colorimetry by Discrete Analyser. This method is
compliant with NEPM (1999) Schedule B(3) (Appdx. 2)
Nitrite as N by Discrete Analyser EK057G WATER APHA 21st ed., 4500-NO2- B. Nitrite is determined by direct colourimetry by Discrete Analyser. This method is
compliant with NEPM (1999) Schedule B(3) (Appdx. 2)
Nitrate as N by Discrete Analyser EK058G WATER APHA 21st ed.. 4500-NO3- F. Nitrate is reduced to nitrite by way of a cadmium reduction column followed by
quantification by Discrete Analyser. Nitrite is determined seperately by direct colourimetry and result for Nitrate
calculated as the difference between the two results This method is compliant with NEPM (1999) Schedule B(3)
(Appdx 2)
Nitrite and Nitrate as N (NOx) by Discrete EK059G WATER APHA 21st ed., 4500-NO3- F. Combined oxidised Nitrogen (N02+NO3) is determined by Cadmium Reduction and
Analyser direct colourimetry by Discrete Analyser. This method is compliant with NEPM (1999) Schedule B(3) (Appdx. 2)
Total Kjeldahl Nitrogen as N By Discrete EK061G WATER APHA 21st ed. 4500-Norg D. 25mL water samples are digested using a traditional Kjeldahl digestion followed by
Analyser determination by Discrete Analyser. This method is compliant with NEPM (1999) Schedule B(3) (Appdx. 2)
Total Nitrogen as N (TKN + Nox) By EK062G WATER APHA 21st ed., 4500-Norg / 4500-NO3-. This method is compliant with NEPM (1999) Schedule B(3) (Appdx. 2)
Discrete Analyser
Total Phosphorus as P By Discrete EK067G WATER APHA 21st ed., 4500-P B&F This procedure involves sulphuric acid digestion of a 100mL sample to break
Analyser phosphorus down to orthophosphate. The orthophosphate reacts with ammonium molybdate and antimony
potassium tartrate to form a complex which is then reduced and its concentration measured at 880nm using
Discrete Analyser. This method is compliant with NEPM (1999) Schedule B(3) (Appdx, 2)
Reactive Phosphorus as P-By Discrete EK071G WATER APHA 21st ed., 4500-P F Ammonium molybdate and potassium antimonyl tartrate reacts in acid medium with
Analyser othophosphate to form a heteropoly acid -phosphomolybdic acid - which is reduced to intensely coloured
molybdenum blue by ascorbic acid. Quantification is by Discrete Analyser This method is compliant with NEPM
(1999) Schedule B(3) (Appdx. 2)
Dissolved Organic Carbon EP002 WATER APHA 21st ed., 5310 B. This method is compliant with NEPM (1999) Schedule B(3) (Appdx. 2)
TPH - Semrvolatile Fraction EP071 WATER USEPA SW 846 - 8015A The sample extract is analysed by Capillary GC/FID and quantification is by comparison
against an established 5 point calibration curve of n-Alkane standards. This method is compliant with NEPM
(1999) Schedule B(3) (Appdx. 2)
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