13.060.60 - Examination of physical properties of water
ICS 13.060.60 Details
Examination of physical properties of water
Untersuchung von Wasser auf physikalische Eigenschaften
Détermination des propriétés physiques de l'eau
Preiskava fizikalnih lastnosti vode
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This document specifies the determination of radium-226 (226Ra) activity concentration in non-saline
water samples by extraction of its daughter radon-222 (222Rn) and its measurement using liquid
scintillation analysis.
The test method described in this document, using currently available scintillation counters, has a
detection limit of approximately 50 mBq·l−1. This method is not applicable to the measurement of other
radium isotopes.
- Standard24 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies the determination of radium-226 (226Ra) activity concentration in non-saline
water samples by extraction of its daughter radon-222 (222Rn) and its measurement using liquid
scintillation analysis.
The test method described in this document, using currently available scintillation counters, has a
detection limit of approximately 50 mBq·l−1. This method is not applicable to the measurement of other
radium isotopes.
- Standard24 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies methods to determine 226Ra concentration by inductively coupled plasma mass spectrometry (ICP-MS). The mass concentrations obtained can be converted into activity concentrations. The method is applicable to test samples of drinking water, rainwater, surface and ground water, after proper sampling and handling, and test sample preparation. The detection limit depends on the sample volume, the instrument used, the background count rate, the detection efficiency, the counting time and the chemical yield. The detection limit of the method described in this document, using currently available equipment, is approximately 10 mBq·l-1, which is better than the WHO criteria for safe consumption of drinking water (1 Bq·l-1). This method covers the measurement of 226Ra in water at activity concentrations between 0,001 Bq·l−1 and 100 Bq·l−1. Samples with concentrations higher than 1 Bq·l−1 can be measured if a dilution is performed. The method described in this document is applicable in the event of an emergency situation. In this method, filtration of the test sample is necessary. The analysis of 226Ra adsorbed to suspended matter is not covered by this method. The analysis of the insoluble fraction requires a mineralization step that is not covered by this document. In this case, the measurement is made on the different phases obtained. It is the user’s responsibility to ensure the validity of this test method for the water samples tested.
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This document specifies a method for the simultaneous measurement of 3H and 14C in water samples by liquid scintillation counting of a source obtained by mixing the water sample with a hydrophilic scintillation cocktail. The method presented in this document is considered a screening method because of the potential presence of interfering radionuclides in the test sample. However, if the sample is known to be free of interfering radionuclides then 3H and 14C can be measured quantitatively. The method can be used for any type of environmental study or monitoring. This method is applicable to test samples of supply/drinking water, rainwater, surface and ground water, marine water, as well as cooling water, industrial water, domestic, and industrial wastewater having an activity concentration ranging from 5 Bq∙l-1 to 106 Bq∙l-1 (upper limit of the liquid scintillation counters for direct counting). For higher activity concentrations, the sample can be diluted to obtain a test sample within this range.
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This document specifies a test method to determine the activity concentration of 227Ac in all types of waters by alpha spectrometry. The test method is applicable to test samples of supply/drinking water, rainwater, surface and ground water, marine water, as well as cooling water, industrial water, domestic, and industrial wastewater after proper sampling and handling and test sample preparation (see ISO 5667-1, ISO 5667-3, ISO 5667-10). Filtration of the test sample is necessary. The detection limit depends on the sample volume, the instrument used, the background count rate, the detection efficiency, the counting time, the chemical yield, and the progeny ingrowth. The method described in this document, using currently available alpha spectrometry apparatus, has a detection limit of approximately 0,03 Bq·l−1, when directly measuring the alpha peak of 227Ac. This detection limit is lower than the WHO criteria for safe consumption of drinking water for any actinide alpha emitter (0,1 Bq·l−1).[4] This value can be achieved with a counting time of 48 h for a sample volume of 1 l. Only a small fraction of 227Ac decays through alpha emissions (~1,42 %). An option to lower the detection limit of the method is to wait, let the progenies of 227Ac grow in, and measure an alpha progeny peak of 227Ac (e.g. 215Po). This is a longer technique, but a lower detection limit of approximately 0,000 2 Bq·l−1 can be obtained by re-counting the sample approximately 90 days after purification. The sample can be re-counted before 90 days, but with a higher detection limit. The test method(s) described in this document can be used during planned, existing and emergency exposure situations as well as for wastewaters and liquid effluents with specific modifications that can increase the overall uncertainty, detection limit and threshold. For an emergency situation, it is preferable to reduce the counting time rather than the sample volume. The analysis of 227Ac adsorbed to suspended matter is not covered by this document.
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ISO 13164-4:2015 describes a test method for the determination of radon-222 (222Rn) activity concentration in non-saline waters by extraction and liquid scintillation counting.
The radon-222 activity concentrations, which can be measured by this test method utilizing currently available instruments, are at least above 0,5 Bq l−1 for a 10 ml test sample and a measuring time of 1 h.
This test method can be used successfully with drinking water samples and it is the responsibility of the laboratory to ensure the validity of this test method for water samples of untested matrices.
Annex A gives indication on the necessary counting conditions to meet the required detection limits for drinking water monitoring.
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This document specifies the method and the conditions for the determination of 232Th activity concentration in samples of environmental water (including sea waters) and waste waters before release to the environment using alpha spectrometry and 229Th as a recovery tracer. A chemical separation allows to separate and purify thorium from a test portion of the sample. The general principles outlined in this document can be applied for the analysis of other alpha-emitting thorium isotopes such as 228Th and 230Th in aqueous samples.
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This document describes a test method for the determination of radon-222 (222Rn) activity concentration in non-saline waters by extraction and liquid scintillation counting.
The 222Rn activity concentrations, which can be measured by this test method utilizing currently available instruments, are above 0,5 Bq·l−1 which is the typical detection limit for a 10 ml test sample and a measuring time of 1 h.
It is the responsibility of the laboratory to ensure the validity of this test method for water samples of untested matrices.
Annex A gives indication on the necessary counting conditions to meet the required detection limits for drinking water monitoring.
- Standard25 pagesEnglish languagesale 10% offe-Library read for1 day
This document describes a test method for the determination of radon-222 (222Rn) activity concentration in non-saline waters by extraction and liquid scintillation counting. The 222Rn activity concentrations, which can be measured by this test method utilizing currently available instruments, are above 0,5 Bq·l−1 which is the typical detection limit for a 10 ml test sample and a measuring time of 1 h. It is the responsibility of the laboratory to ensure the validity of this test method for water samples of untested matrices. Annex A gives indication on the necessary counting conditions to meet the required detection limits for drinking water monitoring.
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This document specifies a test method for measuring actinides (238Pu, 239+240Pu, 241Am, 242Cm, 243+244Cm and 237Np) in water samples by alpha spectrometry following a chemical separation. This method can be used for any type of environmental study or monitoring after appropriate sampling and handling, and test sample preparation. The detection limit of the test method is 5 × 10−3 Bq·l-1 to 5 × 10−4 Bq·l-1 for a volume of test portion between 0,1 l to 5 l with a counting time of two to ten days. This is lower than the WHO criteria for safe consumption of drinking water (1 Bq·l-1 or 10 Bq·l-1 depending on radionuclide).[4] The method described in this document is applicable in the event of an emergency situation.
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This document specifies a test method to determine radium-226 (226Ra) activity concentration in all types of water by emanometry.
The test method specified is suitable for the determination of the soluble, suspended and total 226Ra activity concentration in all types of water with soluble 226Ra activity concentrations greater than 0,02 Bq l−1.
The decay chains of 238U and 232Th are given in Annex A. Figure A.1 shows the 238U and its decay chain.
- Standard25 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies the determination of radium-226 (226Ra) activity concentration in non-saline water samples by extraction of its daughter radon-222 (222Rn) and its measurement using liquid scintillation analysis. The test method described in this document, using currently available scintillation counters, has a detection limit of approximately 50 mBq·l−1. This method is not applicable to the measurement of other radium isotopes.
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This document specifies a test method to determine radium-226 (226Ra) activity concentration in all types of water by emanometry.
The test method specified is suitable for the determination of the soluble, suspended and total 226Ra activity concentration in all types of water with soluble 226Ra activity concentrations greater than 0,02 Bq l−1.
The decay chains of 238U and 232Th are given in Annex A. Figure A.1 shows the 238U and its decay chain.
- Standard25 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies a method for the measurement of 210Pb in all types of waters by liquid scintillation counting (LSC).
The method is applicable to test samples of supply/drinking water, rainwater, surface and ground water, as well as cooling water, industrial water, domestic, and industrial wastewater after proper sampling and handling, and test sample preparation. Filtration of the test sample is necessary. Lead‑210 activity concentration in the environment can vary and usually ranges from 2 mBq l-1 to 300 mBq l-1 [27][28].
Using currently available liquid scintillation counters, the limit of detection of this method for 210Pb is generally of the order of 20 mBq l-1 to 50 mBq l-1, which is lower than the WHO criteria for safe consumption of drinking water (100 mBq l−1).[4][6] These values can be achieved with a counting time between 180 min and 720 min for a sample volume from 0,5 l to 1,5 l. Higher activity concentrations can be measured by either diluting the sample or using smaller sample aliquots or both. The method presented in this document is not intended for the determination of an ultra-trace amount of 210Pb.
The range of application depends on the amount of dissolved material in the water and on the performance characteristics of the measurement equipment (background count rate and counting efficiency).
The method described in this document is applicable to an emergency situation.
The analysis of Pb adsorbed to suspended matter is not covered by this method.
It is the user’s responsibility to ensure the validity of this test method for the water samples tested.
- Standard30 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies a test method to determine radium-226 (226Ra) activity concentration in all types of water by emanometry. The test method specified is suitable for the determination of the soluble, suspended and total 226Ra activity concentration in all types of water with soluble 226Ra activity concentrations greater than 0,02 Bq l−1. The decay chains of 238U and 232Th are given in Annex A. Figure A.1 shows the 238U and its decay chain.
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This document specifies the determination of nickel-59 and nickel-63 (59Ni and 63Ni) activity concentration in samples of all types of water using liquid scintillation counting (LSC). Using currently available liquid scintillation counters, this test method can measure 59Ni activity concentrations of 50 mBq·l−1 and 63Ni activity concentrations of 20 mBq·l−1 with a counting time of 200 min and a sample volume of 1,5 l. NOTE These performance indicators are wholly dependent on the measurement regimes in individual laboratories; in particular, the detection limits for 59Ni are entirely dependent on the levels of 63Ni that can be present. The range of application depends on the amount of dissolved material in the water and on the performance characteristics of the measurement equipment (background count rate and detection efficiency). It is the laboratory’s responsibility to ensure the suitability of this test method for the water samples tested.
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This document specifies the determination of nickel-59 and nickel-63 (59Ni and 63Ni) activity concentration in samples of all types of water using inductively coupled plasma mass spectrometry (ICP-MS). Using currently available ICP-MS, this test method can measure 59Ni activity concentrations of 300 mBq⋅l−1 and 63Ni activity concentrations of 200 Bq⋅l−1. These values can be achieved with a sample volume of 1,0 l. Higher activity concentrations can be measured by either diluting the sample or using smaller sample aliquots or both. NOTE These performance indicators are wholly dependent on the measurement regimes in individual laboratories; in particular, the detection limit is influenced by amount of stable nickel present. The range of application depends on the amount of dissolved material in the water and on the performance characteristics of the measurement equipment (background count rate and counting efficiency). It is the laboratory’s responsibility to ensure the suitability of this test method for the water samples tested.
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This document specifies a method for the measurement of 210Pb in all types of waters by liquid
scintillation counting (LSC).
The method is applicable to test samples of supply/drinking water, rainwater, surface and ground water,
as well as cooling water, industrial water, domestic, and industrial wastewater after proper sampling
and handling, and test sample preparation. Filtration of the test sample is necessary. Lead‑210 activity
concentration in the environment can vary and usually ranges from 2 mBq l
-1 to 300 mBq l
-1 [27][28].
Using currently available liquid scintillation counters, the limit of detection of this method for 210Pb
is generally of the order of 20 mBq l
-1 to 50 mBq l
-1, which is lower than the WHO criteria for safe
consumption of drinking water (100 mBq l−1).[4][6]
These values can be achieved with a counting time
between 180 min and 720 min for a sample volume from 0,5 l to 1,5 l. Higher activity concentrations
can be measured by either diluting the sample or using smaller sample aliquots or both. The method
presented in this document is not intended for the determination of an ultra-trace amount of 210Pb.
The range of application depends on the amount of dissolved material in the water and on the
performance characteristics of the measurement equipment (background count rate and counting
efficiency).
The method described in this document is applicable to an emergency situation.
The analysis of Pb adsorbed to suspended matter is not covered by this method.
It is the user’s responsibility to ensure the validity of this test method for the water samples tested.
- Standard30 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies conditions for the determination of 90Sr and 89Sr activity concentration in samples of environmental water using liquid scintillation counting (LSC) or proportional counting (PC).
The method is applicable to test samples of drinking water, rainwater, surface and ground water, marine water, as well as cooling water, industrial water, domestic, and industrial wastewater after proper sampling and handling, and test sample preparation. Filtration of the test sample and a chemical separation are required to separate and purify strontium from a test portion of the sample.
The detection limit depends on the sample volume, the instrument used, the sample count time, the background count rate, the detection efficiency and the chemical yield. The method described in this document, using currently available LSC counters, has a detection limit of approximately 10 mBq l−1 and 2 mBq l−1 for 89Sr and 90Sr, respectively, which is lower than the WHO criteria for safe consumption of drinking water (100 Bq·l−1 for 89Sr and 10 Bq·l−1 for 90Sr)[3]. These values can be achieved with a counting time of 1 000 min for a sample volume of 2 l.
The methods described in this document are applicable in the event of an emergency situation. When fallout occurs following a nuclear accident, the contribution of 89Sr to the total amount of radioactive strontium is not negligible. This document provides test methods to determine the activity concentration of 90Sr in presence of 89Sr.
The analysis of 90Sr and 89Sr adsorbed to suspended matter is not covered by this method.
It is the user’s responsibility to ensure the validity of this test method selected for the water samples tested.
- Standard51 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies a method for the physical pre-treatment and conditioning of water samples and the determination of the activity concentration of various radionuclides emitting gamma-rays with energies between 40 keV and 2 MeV, by gamma‑ray spectrometry according to the generic test method described in ISO 20042.
The method is applicable to test samples of drinking water, rainwater, surface and ground water as well as cooling water, industrial water, domestic and industrial wastewater after proper sampling, sample handling, and test sample preparation (filtration when necessary and taking into account the amount of dissolved material in the water). This method is only applicable to homogeneous samples or samples which are homogeneous via timely filtration.
The lowest limit that can be measured without concentration of the sample or by using only passive shield of the detection system is about 5·10-2 Bq/l for e.g. 137Cs.1 The upper limit of the activity corresponds to a dead time of 10 %. Higher dead times may be used but evidence of the accuracy of the dead-time correction is required.
Depending on different factors, such as the energy of the gamma-rays, the emission probability per nuclear disintegration, the size and geometry of the sample and the detector, the shielding, the counting time and other experimental parameters, the sample may require to be concentrated by evaporation if activities below 5·10-2 Bq/l need to be measured. However, volatile radionuclides (e.g. radon and radioiodine) can be lost during the source preparation.
This method is suitable for application in emergency situations.
1The sample geometry: 3l Marinelli beaker; detector: GE HP N relative efficiency 55 % ; counting time: 18h.
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This document specifies a method for the measurement of 14C activity concentration in all types of water samples by liquid scintillation counting (LSC) either directly on the test sample or following a chemical separation.
The method is applicable to test samples of supply/drinking water, rainwater, surface and ground water, marine water, as well as cooling water, industrial water, domestic, and industrial wastewater.
The detection limit depends on the sample volume, the instrument used, the sample counting time, the background count rate, the detection efficiency and the chemical recovery. The method described in this document, using currently available liquid scintillation counters and suitable technical conditions, has a detection limit as low as 1 Bq∙l−1, which is lower than the WHO criteria for safe consumption of drinking water (100 Bq·l-1). 14C activity concentrations can be measured up to 106 Bq∙l-1 without any sample dilution.
It is the user’s responsibility to ensure the validity of this test method for the water samples tested.
- Standard32 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies conditions for the determination of 90Sr and 89Sr activity concentration in
samples of environmental water using liquid scintillation counting (LSC) or proportional counting (PC).
The method is applicable to test samples of drinking water, rainwater, surface and ground water,
marine water, as well as cooling water, industrial water, domestic, and industrial wastewater after
proper sampling and handling, and test sample preparation. Filtration of the test sample and a chemical
separation are required to separate and purify strontium from a test portion of the sample.
The detection limit depends on the sample volume, the instrument used, the sample count time, the
background count rate, the detection efficiency and the chemical yield. The method described in this
document, using currently available LSC counters, has a detection limit of approximately 10 mBq l−1
and 2 mBq l−1 for 89Sr and 90Sr, respectively, which is lower than the WHO criteria for safe consumption
of drinking water (100 Bq·l−1 for 89Sr and 10 Bq·l−1 for 90Sr)[3]. These values can be achieved with a
counting time of 1 000 min for a sample volume of 2 l.
The methods described in this document are applicable in the event of an emergency situation.
When fallout occurs following a nuclear accident, the contribution of 89Sr to the total amount of
radioactive strontium is not negligible. This document provides test methods to determine the activity
concentration of 90Sr in presence of 89Sr.
The analysis of 90Sr and 89Sr adsorbed to suspended matter is not covered by this method.
It is the user’s responsibility to ensure the validity of this test method selected for the water samples
tested.
- Standard51 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies a method for the physical pre-treatment and conditioning of water samples
and the determination of the activity concentration of various radionuclides emitting gamma-rays with
energies between 40 keV and 2 MeV, by gamma‑ray spectrometry according to the generic test method
described in ISO 20042.
The method is applicable to test samples of drinking water, rainwater, surface and ground water as well
as cooling water, industrial water, domestic and industrial wastewater after proper sampling, sample
handling, and test sample preparation (filtration when necessary and taking into account the amount
of dissolved material in the water). This method is only applicable to homogeneous samples or samples
which are homogeneous via timely filtration.
The lowest limit that can be measured without concentration of the sample or by using only passive
shield of the detection system is about 5·10-2 Bq/l for e.g. 137Cs1). The upper limit of the activity
corresponds to a dead time of 10 %. Higher dead times may be used but evidence of the accuracy of the
dead-time correction is required.
Depending on different factors, such as the energy of the gamma-rays, the emission probability per
nuclear disintegration, the size and geometry of the sample and the detector, the shielding, the counting
time and other experimental parameters, the sample may require to be concentrated by evaporation
if activities below 5·10-2 Bq/l need to be measured. However, volatile radionuclides (e.g. radon and
radioiodine) can be lost during the source preparation.
This method is suitable for application in emergency situations.
- Standard37 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies a method for the measurement of 14C activity concentration in all types of
water samples by liquid scintillation counting (LSC) either directly on the test sample or following a
chemical separation.
The method is applicable to test samples of supply/drinking water, rainwater, surface and ground water,
marine water, as well as cooling water, industrial water, domestic, and industrial wastewater.
The detection limit depends on the sample volume, the instrument used, the sample counting time, the
background count rate, the detection efficiency and the chemical recovery. The method described in
this document, using currently available liquid scintillation counters and suitable technical conditions,
has a detection limit as low as 1 Bq∙l−1, which is lower than the WHO criteria for safe consumption of
drinking water (100 Bq·l-1). 14C activity concentrations can be measured up to 106 Bq∙l-1 without any
sample dilution.
It is the user’s responsibility to ensure the validity of this test method for the water samples tested.
- Standard32 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies conditions for the determination of 90Sr and 89Sr activity concentration in samples of environmental water using liquid scintillation counting (LSC) or proportional counting (PC). The method is applicable to test samples of drinking water, rainwater, surface and ground water, marine water, as well as cooling water, industrial water, domestic, and industrial wastewater after proper sampling and handling, and test sample preparation. Filtration of the test sample and a chemical separation are required to separate and purify strontium from a test portion of the sample. The detection limit depends on the sample volume, the instrument used, the sample count time, the background count rate, the detection efficiency and the chemical yield. The method described in this document, using currently available LSC counters, has a detection limit of approximately 10 mBq l−1 and 2 mBq l−1 for 89Sr and 90Sr, respectively, which is lower than the WHO criteria for safe consumption of drinking water (100 Bq·l−1 for 89Sr and 10 Bq·l−1 for 90Sr)[3]. These values can be achieved with a counting time of 1 000 min for a sample volume of 2 l. The methods described in this document are applicable in the event of an emergency situation. When fallout occurs following a nuclear accident, the contribution of 89Sr to the total amount of radioactive strontium is not negligible. This document provides test methods to determine the activity concentration of 90Sr in presence of 89Sr. The analysis of 90Sr and 89Sr adsorbed to suspended matter is not covered by this method. It is the user’s responsibility to ensure the validity of this test method selected for the water samples tested.
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This document specifies a method for the measurement of 210Pb in all types of waters by liquid scintillation counting (LSC). The method is applicable to test samples of supply/drinking water, rainwater, surface and ground water, as well as cooling water, industrial water, domestic, and industrial wastewater after proper sampling and handling, and test sample preparation. Filtration of the test sample is necessary. Lead‑210 activity concentration in the environment can vary and usually ranges from 2 mBq l-1 to 300 mBq l-1 [27][28]. Using currently available liquid scintillation counters, the limit of detection of this method for 210Pb is generally of the order of 20 mBq l-1 to 50 mBq l-1, which is lower than the WHO criteria for safe consumption of drinking water (100 mBq l−1).[4][6] These values can be achieved with a counting time between 180 min and 720 min for a sample volume from 0,5 l to 1,5 l. Higher activity concentrations can be measured by either diluting the sample or using smaller sample aliquots or both. The method presented in this document is not intended for the determination of an ultra-trace amount of 210Pb. The range of application depends on the amount of dissolved material in the water and on the performance characteristics of the measurement equipment (background count rate and counting efficiency). The method described in this document is applicable to an emergency situation. The analysis of Pb adsorbed to suspended matter is not covered by this method. It is the user’s responsibility to ensure the validity of this test method for the water samples tested.
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This standard specifies a method for the measurement of iron-55 and nickel-63 (55Fe and 63Ni)in all types of waters by liquid scintillation counting (LSC).
The detection limit depends on the sample volume and the instrument used. The test method described in this standard is based on currently available LSC counters.
- Standard30 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies a method for the physical pre-treatment and conditioning of water samples and the determination of the activity concentration of various radionuclides emitting gamma-rays with energies between 40 keV and 2 MeV, by gamma‑ray spectrometry according to the generic test method described in ISO 20042. The method is applicable to test samples of drinking water, rainwater, surface and ground water as well as cooling water, industrial water, domestic and industrial wastewater after proper sampling, sample handling, and test sample preparation (filtration when necessary and taking into account the amount of dissolved material in the water). This method is only applicable to homogeneous samples or samples which are homogeneous via timely filtration. The lowest limit that can be measured without concentration of the sample or by using only passive shield of the detection system is about 5·10-2 Bq/l for e.g. 137Cs.1 The upper limit of the activity corresponds to a dead time of 10 %. Higher dead times may be used but evidence of the accuracy of the dead-time correction is required. Depending on different factors, such as the energy of the gamma-rays, the emission probability per nuclear disintegration, the size and geometry of the sample and the detector, the shielding, the counting time and other experimental parameters, the sample may require to be concentrated by evaporation if activities below 5·10-2 Bq/l need to be measured. However, volatile radionuclides (e.g. radon and radioiodine) can be lost during the source preparation. This method is suitable for application in emergency situations. 1The sample geometry: 3l Marinelli beaker; detector: GE HP N relative efficiency 55 % ; counting time: 18h.
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This document specifies a method for the measurement of 14C activity concentration in all types of water samples by liquid scintillation counting (LSC) either directly on the test sample or following a chemical separation. The method is applicable to test samples of supply/drinking water, rainwater, surface and ground water, marine water, as well as cooling water, industrial water, domestic, and industrial wastewater. The detection limit depends on the sample volume, the instrument used, the sample counting time, the background count rate, the detection efficiency and the chemical recovery. The method described in this document, using currently available liquid scintillation counters and suitable technical conditions, has a detection limit as low as 1 Bq∙l−1, which is lower than the WHO criteria for safe consumption of drinking water (100 Bq·l-1). 14C activity concentrations can be measured up to 106 Bq∙l-1 without any sample dilution. It is the user’s responsibility to ensure the validity of this test method for the water samples tested.
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This document specifies a test method for the determination of iron-55 (55Fe) activity concentration in samples of all types of water using liquid scintillation counting (LSC). Using currently available liquid scintillation counters, this test method can measure the 55Fe activity concentrations in the range from the limit of detection up to 120 mBq l-1. These values can be achieved with a counting time between 7 200 s and 10 800 s for a sample volume from 0,5 l to 1,5 l. Higher activity concentrations can be measured by either diluting the sample or using smaller sample aliquots or both. NOTE These performance indicators are wholly dependent on the measurement regimes in individual laboratories; in particular, the detection limits are influenced by amount of stable iron present. The range of application depends on the amount of dissolved material in the water and on the performance characteristics of the measurement equipment (background count rate and counting efficiency). It is the laboratory’s responsibility to ensure the suitability of this test method for the water samples tested.
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This document provides guidelines for testing laboratories wanting to use rapid test methods on water samples that may be contaminated following a nuclear or radiological emergency incident. In an emergency situation, consideration should be given to:
— taking into account the specific context for the tests to be performed, e.g. a potentially high level of contamination;
— using or adjusting, when possible, radioactivity test methods implemented during routine situations to obtain a result rapidly or, for tests not performed routinely, applying specific rapid test methods previously validated by the laboratory, e.g. for 89Sr determination;
— preparing the test laboratory to measure a large number of potentially contaminated samples.
The aim of this document is to ensure decision makers have reliable results needed to take actions quickly and minimize the radiation dose to the public.
Measurements are performed in order to minimize the risk to the public by checking the quality of water supplies. For emergency situations, test results are often compared to operational intervention levels.
NOTE Operational intervention levels (OILs) are derived from IAEA Safety Standards[8] or national authorities[9].
A key element of rapid analysis can be the use of routine methods but with a reduced turnaround time. The goal of these rapid measurements is often to check for unusual radioactivity levels in the test sample, to identify the radionuclides present and their activity concentration levels and to establish compliance of the water with intervention levels[10][11][12]. It should be noted that in such circumstances, validation parameters evaluated for routine use (e.g. reproducibility, precision, etc.) may not be applicable to the modified rapid method. However, due to the circumstances arising after an emergency, the modified method may still be fit-for-purpose although uncertainties associated with the test results need to be evaluated and may increase from routine analyses.
The first steps of the analytical approach are usually screening methods based on gross alpha and gross beta test methods (adaptation of ISO 10704 and ISO 11704) and gamma spectrometry (adaptation of ISO 20042, ISO 10703 and ISO 19581). Then, if required[13], test method standards for specific radionuclides (see Clause 2) are adapted and applied (for example, 90Sr measurement according to ISO 13160) as proposed in Annex A.
This document refers to published ISO documents. When appropriate, this document also refers to national standards or other publicly available documents.
Screening techniques that can be carried out directly in the field are not part of this document.
- Standard29 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies a method for the measurement of 210Po in all types of waters by alpha spectrometry.
The method is applicable to test samples of supply/drinking water, rainwater, surface and ground water, marine water, as well as cooling water, industrial water, domestic, and industrial wastewater after proper sampling and handling, and test sample preparation. Filtration of the test sample may be required.
The detection limit depends on the sample volume, the instrument used, the counting time, the background count rate, the detection efficiency and the chemical yield. The method described in this document, using currently available alpha spectrometry apparatus, has a detection limit of approximately 5 mBq l−1, which is lower than the WHO criteria for safe consumption of drinking water (100 mBq l−1). This value can be achieved with a counting time of 24 h for a sample volume of 500 ml.
The method described in this document is also applicable in an emergency situation.
The analysis of 210Po adsorbed to suspended matter in the sample is not covered by this method.
If suspended material has to be removed or analysed, filtration using a 0,45 μm filter is recommended. The analysis of the insoluble fraction requires a mineralization step that is not covered by this document [13]. In this case, the measurement is made on the different phases obtained. The final activity is the sum of all the measured activity concentrations.
It is the user's responsibility to ensure the validity of this test method for the water samples tested.
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This standard describes the requirements for rapid testing of water samples under emergency situations in laboratories:
- taking into account a special context for analyses, e.g. an unknown and unusual contamination;
- using or adapting if possible radioactivity measurements methods used in routine to get a result
rapidly or applying specific rapid methods previously tested by the laboratory, e.g. for 89Sr determination ;
- preparing the laboratory to analyse a large number of potentially contaminated samples.
The focus thereby is on cases where rapid radioactivity test methods are applied for all kind of waters. The first steps of the analytical strategy is often based on gross alpha and gross beta as screening methods (adaptation of ISO 10704 and ISO 11704) and gamma spectrometry (adaptation of ISO 10703). Then if necessary, specific radionuclides standards are adapted and applied (for example, Strontium 90 measurement following ISO 13160).
This guideline refers to a number of ISO standards. If appropriate, it will also refer to national or other
publically available standards.
Screening techniques that can be carried out on site are not part of this guide.
- Standard29 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies a method for the measurement of 210Po in all types of waters by alpha
spectrometry.
The method is applicable to test samples of supply/drinking water, rainwater, surface and ground
water, marine water, as well as cooling water, industrial water, domestic, and industrial wastewater
after proper sampling and handling, and test sample preparation. Filtration of the test sample may be
required.
The detection limit depends on the sample volume, the instrument used, the counting time, the
background count rate, the detection efficiency and the chemical yield. The method described in
this document, using currently available alpha spectrometry apparatus, has a detection limit of
approximately 5 mBq l−1, which is lower than the WHO criteria for safe consumption of drinking water
(100 mBq l−1). This value can be achieved with a counting time of 24 h for a sample volume of 500 ml.
The method described in this document is also applicable in an emergency situation.
The analysis of 210Po adsorbed to suspended matter in the sample is not covered by this method.
If suspended material has to be removed or analysed, filtration using a 0,45 μm filter is recommended.
The analysis of the insoluble fraction requires a mineralization step that is not covered by this document
[13]. In this case, the measurement is made on the different phases obtained. The final activity is the
sum of all the measured activity concentrations.
It is the user’s responsibility to ensure the validity of this test method for the water samples tested.
- Standard28 pagesEnglish languagesale 10% offe-Library read for1 day
ISO 13164-3:2013 specifies a test method for the determination of radon-222 activity concentration in a sample of water following its transfer from the aqueous phase to the air phase by degassing and its detection. It gives recommendations for rapid measurements performed within less than 1 h.
The radon-222 activity concentrations, which can be measured by this test method utilizing currently available instruments, range from 0,1 Bq l−1 to several hundred thousand becquerels per litre for a 100 ml test sample.
This test method is used successfully with drinking water samples. The laboratory is responsible for ensuring the validity of this test method for water samples of untested matrices.
This test method can be applied on field sites or in the laboratory.
Annexes A and B give indications on the necessary counting conditions to meet the required sensitivity for drinking water monitoring
- Standard31 pagesEnglish languagesale 10% offe-Library read for1 day
ISO 13164-1:2013 gives general guidelines for sampling, packaging, and transporting of all kinds of water samples, for the measurement of the activity concentration of radon-222.
The test methods fall into two categories: a) direct measurement of the water sample without any transfer of phase (see ISO 13164‑2); b) indirect measurement involving the transfer of the radon-222 from the aqueous phase to another phase (see ISO 13164‑3).
The test methods can be applied either in the laboratory or on site.
The laboratory is responsible for ensuring the suitability of the test method for the water samples tested.
- Standard33 pagesEnglish languagesale 10% offe-Library read for1 day
ISO 13164-2:2013 specifies a test method for the determination of radon-222 activity concentration in a sample of water following the measurement of its short-lived decay products by direct gamma-spectrometry of the water sample.
The radon-222 activity concentrations, which can be measured by this test method utilizing currently available gamma-ray instruments, range from a few becquerels per litre to several hundred thousand becquerels per litre for a 1 l test sample.
This test method can be used successfully with drinking water samples. The laboratory is responsible for ensuring the validity of this test method for water samples of untested matrices.
An annex gives indications on the necessary counting conditions to meet the required sensitivity for drinking water monitoring.
- Standard21 pagesEnglish languagesale 10% offe-Library read for1 day
ISO 13165-3:2016 specifies the determination of radium-226 (226Ra) activity concentration in all types of water by coprecipitation followed by gamma-spectrometry (see ISO 18589‑3).
The method described is suitable for determination of soluble 226Ra activity concentrations greater than 0,02 Bq l−1 using a sample volume of 1 l to 100 l of any water type.
For water samples smaller than a volume of 1 l, direct gamma-spectrometry can be performed following ISO 10703 with a higher detection limit.
NOTE This test method also allows other isotopes of radium, 223Ra, 224Ra, and 228Ra, to be determined.
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This document specifies the determination of radium-226 (226Ra) and radium-228 (228Ra) activity concentrations in drinking water samples by chemical separation of radium and its measurement using liquid scintillation counting.
Massic activity concentrations of 226Ra and 228Ra which can be measured by this test method utilizing currently available liquid scintillation counters go down to 0,01 Bq/kg for 226Ra and 0,06 Bq/kg for 228Ra for a 0,5 kg sample mass and a 1 h counting time in a low background liquid scintillation counter[8].
The test method can be used for the fast detection of contamination of drinking water by radium in emergency situations.
- Standard37 pagesEnglish languagesale 10% offe-Library read for1 day
This document provides guidelines for testing laboratories wanting to use rapid test methods on water samples that may be contaminated following a nuclear or radiological emergency incident. In an emergency situation, consideration should be given to: — taking into account the specific context for the tests to be performed, e.g. a potentially high level of contamination; — using or adjusting, when possible, radioactivity test methods implemented during routine situations to obtain a result rapidly or, for tests not performed routinely, applying specific rapid test methods previously validated by the laboratory, e.g. for 89Sr determination; — preparing the test laboratory to measure a large number of potentially contaminated samples. The aim of this document is to ensure decision makers have reliable results needed to take actions quickly and minimize the radiation dose to the public. Measurements are performed in order to minimize the risk to the public by checking the quality of water supplies. For emergency situations, test results are often compared to operational intervention levels. NOTE Operational intervention levels (OILs) are derived from IAEA Safety Standards[8] or national authorities[9]. A key element of rapid analysis can be the use of routine methods but with a reduced turnaround time. The goal of these rapid measurements is often to check for unusual radioactivity levels in the test sample, to identify the radionuclides present and their activity concentration levels and to establish compliance of the water with intervention levels[10][11][12]. It should be noted that in such circumstances, validation parameters evaluated for routine use (e.g. reproducibility, precision, etc.) may not be applicable to the modified rapid method. However, due to the circumstances arising after an emergency, the modified method may still be fit-for-purpose although uncertainties associated with the test results need to be evaluated and may increase from routine analyses. The first steps of the analytical approach are usually screening methods based on gross alpha and gross beta test methods (adaptation of ISO 10704 and ISO 11704) and gamma spectrometry (adaptation of ISO 20042, ISO 10703 and ISO 19581). Then, if required[13], test method standards for specific radionuclides (see Clause 2) are adapted and applied (for example, 90Sr measurement according to ISO 13160) as proposed in Annex A. This document refers to published ISO documents. When appropriate, this document also refers to national standards or other publicly available documents. Screening techniques that can be carried out directly in the field are not part of this document.
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This document specifies the conditions for the determination of uranium isotope activity concentration in samples of environmental water (including sea waters) using alpha-spectrometry and 232U as a yield tracer. A chemical separation is required to separate and purify uranium from a test portion of the sample.
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This document specifies a method for the measurement of 210Po in all types of waters by alpha spectrometry. The method is applicable to test samples of supply/drinking water, rainwater, surface and ground water, marine water, as well as cooling water, industrial water, domestic, and industrial wastewater after proper sampling and handling, and test sample preparation. Filtration of the test sample may be required. The detection limit depends on the sample volume, the instrument used, the counting time, the background count rate, the detection efficiency and the chemical yield. The method described in this document, using currently available alpha spectrometry apparatus, has a detection limit of approximately 5 mBq l−1, which is lower than the WHO criteria for safe consumption of drinking water (100 mBq l−1). This value can be achieved with a counting time of 24 h for a sample volume of 500 ml. The method described in this document is also applicable in an emergency situation. The analysis of 210Po adsorbed to suspended matter in the sample is not covered by this method. If suspended material has to be removed or analysed, filtration using a 0,45 μm filter is recommended. The analysis of the insoluble fraction requires a mineralization step that is not covered by this document [13]. In this case, the measurement is made on the different phases obtained. The final activity is the sum of all the measured activity concentrations. It is the user's responsibility to ensure the validity of this test method for the water samples tested.
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This document specifies a method for the measurement of 99Tc in all types of water by inductively coupled plasma mass spectrometry (ICP-MS).
The method is applicable to test samples of supply/drinking water, rainwater, surface and ground water, as well as cooling water, industrial water, domestic, and industrial wastewater after proper sampling and handling and test sample preparation. A filtration of the test sample is necessary.
The detection limit depends on the sample volume and the instrument used. The method described in this document, using currently available ICP-MS, has a detection limit of approximately 0,2 ng·kg−1 to 0,5 ng·kg−1 (0,1 Bq·kg−1 to 0,3 Bq·kg−1), which is much lower than the WHO criteria for safe consumption of drinking water (100 Bq·l−1)[3]. The method presented in this document is not intended for the determination of ultra-trace amount of 99Tc.
The mass concentration values in this document are expressed by sample mass unit instead of sample volume unit as it is usually the case in similar standards. The reason is that 99Tc is measured in various matrix types such as fresh water or sea water, which have significant differences in density. The mass concentration values can be easily converted to sample volume unit by measuring the sample volume. However, it increases the uncertainty on the mass concentration result.
The method described in this document is applicable in the event of an emergency situation, but not if 99mTc is present at quantities that could cause interference.
The analysis of Tc adsorbed to suspended matter is not covered by this method.
It is the user's responsibility to ensure the validity of this test method for the water samples tested.
- Standard31 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies a method for the measurement of 99Tc in all types of waters by liquid scintillation counting (LSC).
The method is applicable to test samples of supply/drinking water, rainwater, surface and ground water, as well as cooling water, industrial water, domestic, and industrial wastewater after proper sampling and handling, and test sample preparation. A filtration of the test sample is necessary.
The detection limit depends on the sample volume and the instrument used. The method described in this document, using currently available LSC instruments, has a detection limit of approximately 5 Bq·kg−1 to 20 Bq·kg−1, which is lower than the WHO criteria for safe consumption of drinking water (100 Bq l−1)[3]. These values can be achieved with a counting time of 30 min for a sample volume varying between 14 ml to 40 ml. The method presented in this document is not intended for the determination of ultra-trace amount of 99Tc.
The activity concentration values in this document are expressed by sample mass unit instead of sample volume unit as it is usually the case in similar standards. The reason is that 99Tc is measured in various matrix types such as fresh water or sea water, which have significant differences in density. The activity concentration values can be easily converted to sample volume unit by measuring the sample volume. However, it increases the uncertainty on the activity concentration result.
The method described in this document is applicable in the event of an emergency situation, but not if 99mTc is present at quantities that could cause interference and not if 99mTc is used as a recovery tracer.
The analysis of Tc adsorbed to suspended matter is not covered by this method.
It is the user's responsibility to ensure the validity of this test method for the water samples tested.
- Standard30 pagesEnglish languagesale 10% offe-Library read for1 day
ISO 13164-3:2013 specifies a test method for the determination of radon-222 activity concentration in a sample of water following its transfer from the aqueous phase to the air phase by degassing and its detection. It gives recommendations for rapid measurements performed within less than 1 h.
The radon-222 activity concentrations, which can be measured by this test method utilizing currently available instruments, range from 0,1 Bq l−1 to several hundred thousand becquerels per litre for a 100 ml test sample.
This test method is used successfully with drinking water samples. The laboratory is responsible for ensuring the validity of this test method for water samples of untested matrices.
This test method can be applied on field sites or in the laboratory.
Annexes A and B give indications on the necessary counting conditions to meet the required sensitivity for drinking water monitoring
- Standard31 pagesEnglish languagesale 10% offe-Library read for1 day
ISO 13164-1:2013 gives general guidelines for sampling, packaging, and transporting of all kinds of water samples, for the measurement of the activity concentration of radon-222.
The test methods fall into two categories: a) direct measurement of the water sample without any transfer of phase (see ISO 13164‑2); b) indirect measurement involving the transfer of the radon-222 from the aqueous phase to another phase (see ISO 13164‑3).
The test methods can be applied either in the laboratory or on site.
The laboratory is responsible for ensuring the suitability of the test method for the water samples tested.
- Standard33 pagesEnglish languagesale 10% offe-Library read for1 day
ISO 13165-3:2016 specifies the determination of radium-226 (226Ra) activity concentration in all types of water by coprecipitation followed by gamma-spectrometry (see ISO 18589‑3).
The method described is suitable for determination of soluble 226Ra activity concentrations greater than 0,02 Bq l−1 using a sample volume of 1 l to 100 l of any water type.
For water samples smaller than a volume of 1 l, direct gamma-spectrometry can be performed following ISO 10703 with a higher detection limit.
NOTE This test method also allows other isotopes of radium, 223Ra, 224Ra, and 228Ra, to be determined.
- Standard22 pagesEnglish languagesale 10% offe-Library read for1 day
ISO 13164-2:2013 specifies a test method for the determination of radon-222 activity concentration in a sample of water following the measurement of its short-lived decay products by direct gamma-spectrometry of the water sample.
The radon-222 activity concentrations, which can be measured by this test method utilizing currently available gamma-ray instruments, range from a few becquerels per litre to several hundred thousand becquerels per litre for a 1 l test sample.
This test method can be used successfully with drinking water samples. The laboratory is responsible for ensuring the validity of this test method for water samples of untested matrices.
An annex gives indications on the necessary counting conditions to meet the required sensitivity for drinking water monitoring.
- Standard21 pagesEnglish languagesale 10% offe-Library read for1 day
This document specifies the determination of radium-226 (226Ra) and radium-228 (228Ra) activity concentrations in drinking water samples by chemical separation of radium and its measurement using liquid scintillation counting. Massic activity concentrations of 226Ra and 228Ra which can be measured by this test method utilizing currently available liquid scintillation counters go down to 0,01 Bq/kg for 226Ra and 0,06 Bq/kg for 228Ra for a 0,5 kg sample mass and a 1 h counting time in a low background liquid scintillation counter[8]. The test method can be used for the fast detection of contamination of drinking water by radium in emergency situations.
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This document specifies a test method for the determination of gross beta activity concentration in non-saline waters. The method covers non-volatile radionuclides with maximum beta energies of approximately 0,3 MeV or higher. Measurement of low energy beta emitters (e.g. 3H, 228Ra, 210Pb, 14C, 35S and 241Pu) and some gaseous or volatile radionuclides (e.g. radon and radioiodine) might not be included in the gross beta quantification using the test method described in this document.
This test method is applicable to the analysis of raw and drinking waters. The range of application depends on the amount of total soluble salts in the water and on the performance characteristics (background count rate and counting efficiency) of the counter used.
It is the laboratory's responsibility to ensure the suitability of this method for the water samples tested.
- Standard21 pagesEnglish languagesale 10% offe-Library read for1 day