Measuring environmental change in forest ecosystems by repeated soil sampling: A North American perspective

Science.gov (United States)

Gregory B. Lawrence; Ivan J. Fernandez; Daniel D. Richter; Donald S. Ross; Paul W. Hazlett; Scott W. Bailey; Rock Ouimet; Richard A. F. Warby; Arthur H. Johnson; Henry Lin; James M. Kaste; Andrew G. Lapenis; Timothy J. Sullivan

2013-01-01

Environmental change is monitored in North America through repeated measurements of weather, stream and river flow, air and water quality, and most recently, soil properties. Some skepticism remains, however, about whether repeated soil sampling can effectively distinguish between temporal and spatial variability, and efforts to document soil change in forest...

Measurements of 222Rn and 226Ra Levels in environmental samples by using liquid scintillation counter

International Nuclear Information System (INIS)

Moustafa, A.S.

2004-01-01

The advantageous of liquid scintillation counting technique for 6 Ra determination compared with other methods are the high counting efficiency and the easier sample preparation, with no need for sample pre-concentration. In this work, liquid scintillation counting system was used to measure 222 Rn and 226 Ra levels in environmental samples. The liquid scintillation cocktail was prepared in the laboratory and was found efficient for measuring 222 Rn. Soil, sediment and TENORM samples were dried, grind, sieved and added to hydrochloric acid, in a standard scintillation vial, preloaded with the liquid scintillation cocktail. By measuring 222 Rn levels in the prepared vials, at different intervals of time after preparation, 222 Rn and 226 Ra levels were determined

Practical reporting times for environmental samples

International Nuclear Information System (INIS)

Bayne, C.K.; Schmoyer, D.D.; Jenkins, R.A.

1993-02-01

Preanalytical holding times for environmental samples are specified because chemical and physical characteristics may change between sampling and chemical analysis. For example, the Federal Register prescribes a preanalytical holding time of 14 days for volatile organic compounds in soil stored at 4 degrees C. The American Society for Testing Materials (ASTM) uses a more technical definition that the preanalytical holding time is the day when the analyte concentration for an environmental sample falls below the lower 99% confidence interval on the analyte concentration at day zero. This study reviews various holding time definitions and suggest a new preanalytical holding time approach using acceptable error rates for measuring an environmental analyte. This practical reporting time (PRT) approach has been applied to nineteen volatile organic compounds and four explosives in three environmental soil samples. A PRT nomograph of error rates has been developed to estimate the consequences of missing a preanalytical holding time. This nomograph can be applied to a large class of analytes with concentrations that decay linearly or exponentially with time regardless of sample matrices and storage conditions

Practical reporting times for environmental samples

Energy Technology Data Exchange (ETDEWEB)

Bayne, C.K.; Schmoyer, D.D.; Jenkins, R.A.

1993-02-01

Preanalytical holding times for environmental samples are specified because chemical and physical characteristics may change between sampling and chemical analysis. For example, the Federal Register prescribes a preanalytical holding time of 14 days for volatile organic compounds in soil stored at 4{degrees}C. The American Society for Testing Materials (ASTM) uses a more technical definition that the preanalytical holding time is the day when the analyte concentration for an environmental sample falls below the lower 99% confidence interval on the analyte concentration at day zero. This study reviews various holding time definitions and suggest a new preanalytical holding time approach using acceptable error rates for measuring an environmental analyte. This practical reporting time (PRT) approach has been applied to nineteen volatile organic compounds and four explosives in three environmental soil samples. A PRT nomograph of error rates has been developed to estimate the consequences of missing a preanalytical holding time. This nomograph can be applied to a large class of analytes with concentrations that decay linearly or exponentially with time regardless of sample matrices and storage conditions.

Isotope dilution analysis of environmental samples

International Nuclear Information System (INIS)

Tolgyessy, J.; Lesny, J.; Korenova, Z.; Klas, J.; Klehr, E.H.

1986-01-01

Isotope dilution analysis has been used for the determination of several trace elements - especially metals - in a variety of environmental samples, including aerosols, water, soils, biological materials and geological materials. Variations of the basic concept include classical IDA, substoichiometric IDA, and more recently, sub-superequivalence IDA. Each variation has its advantages and limitations. A periodic chart has been used to identify those elements which have been measured in environmental samples using one or more of these methods. (author)

Environmental 90Sr measurements

Science.gov (United States)

Paul, M.; Berkovits, D.; Cecil, L.D.; Feldstein, H.; Hershkowitz, A.; Kashiv, Y.; Vogt, S.

1997-01-01

90Sr (T1/2 = 28.5 years) is a long-lived radionuclide produced in nuclear fission. Fast radiochemical detection of 90Sr in environmental samples is not feasible using current analytical methods. Accelerator Mass Spectrometry (AMS) measurements of 90Sr were made with the Rehovot 14UD Pelletron accelerator at a terminal voltage of 11 or 12 MV using our standard detection system. Injection of hydride ions (SrH3-) was chosen owing to high beam intensity and low Coulomb explosion effects. 90Sr ions were identified and discriminated from isobaric 90Zr by measuring time of flight, total energy and three independent energy-loss signals in an ionization chamber. A reference sample and a ground-water sample were successfully measured. The detection limit determined for a laboratory blank by the residual counts in the 90Sr region is 90Sr/Sr = 3 ?? 10-13, corresponding in practice to (2-4) ?? 10790Sr atoms or about 0.5-1 pCi/L in environmental water samples.

Environmental surveillance master sampling schedule

Energy Technology Data Exchange (ETDEWEB)

Bisping, L E

1992-01-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest Laboratory (PNL) for the US Department of Energy (DOE). This document contains the planned schedule for routine sample collection for the Surface Environmental Surveillance Project (SESP) and Ground-Water Monitoring Project. Samples for radiological analyses include Air-Particulate Filter, gases and vapor; Water/Columbia River, Onsite Pond, Spring, Irrigation, and Drinking; Foodstuffs/Animal Products including Whole Milk, Poultry and Eggs, and Beef; Foodstuffs/Produce including Leafy Vegetables, Vegetables, and Fruit; Foodstuffs/Farm Products including Wine, Wheat and Alfalfa; Wildlife; Soil; Vegetation; and Sediment. Direct Radiation Measurements include Terrestrial Locations, Columbia River Shoreline Locations, and Onsite Roadway, Railway and Aerial, Radiation Surveys.

Effects of holding time and measurement error on culturing Legionella in environmental water samples.

Science.gov (United States)

Flanders, W Dana; Kirkland, Kimberly H; Shelton, Brian G

2014-10-01

Outbreaks of Legionnaires' disease require environmental testing of water samples from potentially implicated building water systems to identify the source of exposure. A previous study reports a large impact on Legionella sample results due to shipping and delays in sample processing. Specifically, this same study, without accounting for measurement error, reports more than half of shipped samples tested had Legionella levels that arbitrarily changed up or down by one or more logs, and the authors attribute this result to shipping time. Accordingly, we conducted a study to determine the effects of sample holding/shipping time on Legionella sample results while taking into account measurement error, which has previously not been addressed. We analyzed 159 samples, each split into 16 aliquots, of which one-half (8) were processed promptly after collection. The remaining half (8) were processed the following day to assess impact of holding/shipping time. A total of 2544 samples were analyzed including replicates. After accounting for inherent measurement error, we found that the effect of holding time on observed Legionella counts was small and should have no practical impact on interpretation of results. Holding samples increased the root mean squared error by only about 3-8%. Notably, for only one of 159 samples, did the average of the 8 replicate counts change by 1 log. Thus, our findings do not support the hypothesis of frequent, significant (≥= 1 log10 unit) Legionella colony count changes due to holding. Copyright © 2014 The Authors. Published by Elsevier Ltd.. All rights reserved.

Determination of technetium-99 in environmental samples: A review

International Nuclear Information System (INIS)

Shi Keliang; Hou Xiaolin; Roos, Per; Wu Wangsuo

2012-01-01

Highlights: ► The source term, physicochemical properties, environmental distribution and behaviour of 99 Tc are presented. ► Various sample pre-treatment and pre-concentration techniques of technetium are discussed. ► Chemical separation and purification techniques for 99 Tc in environmental samples are reviewed. ► Measurement techniques for 99 Tc in environmental level and automated analytical methods are reviewed. ► The reported analytical methods of 99 Tc are critically compared to provide overall information. - Abstract: Due to the lack of a stable technetium isotope, and the high mobility and long half-life, 99 Tc is considered to be one of the most important radionuclides in safety assessment of environmental radioactivity as well as nuclear waste management. 99 Tc is also an important tracer for oceanographic research due to the high technetium solubility in seawater as TcO 4 − . A number of analytical methods, using chemical separation combined with radiometric and mass spectrometric measurement techniques, have been developed over the past decades for determination of 99 Tc in different environmental samples. This article summarizes and compares recently reported chemical separation procedures and measurement methods for determination of 99 Tc. Due to the extremely low concentration of 99 Tc in environmental samples, the sample preparation, pre-concentration, chemical separation and purification for removal of the interferences for detection of 99 Tc are the most important issues governing the accurate determination of 99 Tc. These aspects are discussed in detail in this article. Meanwhile, the different measurement techniques for 99 Tc are also compared with respect to advantages and drawbacks. Novel automated analytical methods for rapid determination of 99 Tc using solid extraction or ion exchange chromatography for separation of 99 Tc, employing flow injection or sequential injection approaches are also discussed.

Sampling and chemical analysis in environmental samples around Nuclear Power Plants and some environmental samples

Energy Technology Data Exchange (ETDEWEB)

Cho, Yong Woo; Han, Man Jung; Cho, Seong Won; Cho, Hong Jun; Oh, Hyeon Kyun; Lee, Jeong Min; Chang, Jae Sook [KORTIC, Taejon (Korea, Republic of)

2002-12-15

Twelve kinds of environmental samples such as soil, seawater, underground water, etc. around Nuclear Power Plants(NPPs) were collected. Tritium chemical analysis was tried for the samples of rain water, pine-needle, air, seawater, underground water, chinese cabbage, a grain of rice and milk sampled around NPPs, and surface seawater and rain water sampled over the country. Strontium in the soil that sere sampled at 60 point of district in Korea were analyzed. Tritium were sampled at 60 point of district in Korea were analyzed. Tritium were analyzed in 21 samples of surface seawater around the Korea peninsular that were supplied from KFRDI(National Fisheries Research and Development Institute). Sampling and chemical analysis environmental samples around Kori, Woolsung, Youngkwang, Wooljin Npps and Taeduk science town for tritium and strontium analysis was managed according to plans. Succeed to KINS after all samples were tried.

New methodological approaches to the simultaneous measurement of the 90Sr and 137Cs activity in environmental samples

Directory of Open Access Journals (Sweden)

M. V. Zheltonozhska

2012-12-01

Full Text Available Nonradiochemical method of measurement of 90Sr and137Cs activity in environmental samples is proposed. This method is based on spectrometrical investigation of electrons accompanied the decay of the 90Sr and137Cs. Accounting for the contribution to the total activity of the samples from the zones with the density of the contamination 1 - 5 Кu/km2 the 40K electrons allowed to improve the accuracy of the measurements for the samples of small rodents up to 15 - 20 % (the ratio of A (137Cs/A (90Sr was from 2 to 100, for samples of soil up to 10 - 15 % (the change of activity in these samples was ten thousand times. The results of the spectrometric measurements were confirmed by the traditional radiochemical research.

Collection and preparation of samples for Agency's programme of intercalibration methods and procedures for measurement of environmental radioactivity

International Nuclear Information System (INIS)

Patel, B.

1975-12-01

In the period of 1971-1975 several samples of marine sediment and organisms were collected from the Bombay Harbour Bay as well as from the vicinity of the Tarapur nuclear power station in order to supply the materials for preparing intercalibration samples for radionuclides measurements. All samples collected were freeze-dried and homogenized prior to the dispatch to the Monaco Laboratory, where final homogenization and the homogeneity tests were carried out. Altogether 2 marine organisms and 3 marine sediments were supplied during this period. The materials supplied were proved to be useful to prepare intercalibration samples for radionuclide measurements in the levels for monitoring operations. Based on these materials several intercalibration exercises were successfully conducted. This work thus formed a basis for bringing the better comparability of radionuclide measurements in marine environmental samples in an international scale

Determination of technetium-99 in environmental samples: A review

DEFF Research Database (Denmark)

Shi, Keliang; Hou, Xiaolin; Roos, Per

2012-01-01

Due to the lack of a stable technetium isotope, and the high mobility and long half-life, 99Tc is considered to be one of the most important radionuclides in safety assessment of environmental radioactivity as well as nuclear waste management. 99Tc is also an important tracer for oceanographic...... research due to the high technetium solubility in seawater as TcO4−. A number of analytical methods, using chemical separation combined with radiometric and mass spectrometric measurement techniques, have been developed over the past decades for determination of 99Tc in different environmental samples....... This article summarizes and compares recently reported chemical separation procedures and measurement methods for determination of 99Tc. Due to the extremely low concentration of 99Tc in environmental samples, the sample preparation, pre-concentration, chemical separation and purification for removal...

Environmental radioactivity measurement intercomparison exercise 1990

International Nuclear Information System (INIS)

Jerome, S.M.

1991-05-01

In a recent national intercomparison exercise, 49 laboratories involved in making environmental radioactivity measurements took part in the analysis of samples supplied by the National Physical Laboratory (NPL) in the United Kingdom. There were two sets of samples; one containing pure β-emitters and one containing β/γ-emitters. Two thirds of the participants measured the β/γ-emitter sample only, the remainder measured both. The results are presented. (author)

Criteria for requesting specific radionuclide analysis through gross α and gross β concentration measurements in environmental samples

International Nuclear Information System (INIS)

Ferreira, E.G.

1988-01-01

This paper suggests some criteria for the decision to proceed with the analysis of specific radionuclides based on results of the determination of gross α and β concentrations in environmental samples of aerosols, water, dairy and agricultural products, soil and sediments. The samples considered are provenient from the environmental surveillance of uranium mining and milling facilities as well as the mining and processing plants of monazite sands. The radionuclides to be analysed are those considered to be the most critical to human health, that is: U-nat; Th-nat; Th-230; Ra-228; Ra-226; Po-210; Pb-210. The measured gross α and β concentrations will be compared with the Maximum Allowable Concentrations for some defined radionuclides. Radiochemical analysis of specific radionuclides may then become necessary, depending upon the results of this comparison. The main goal of the proposed guide is to simplify and to discipline the execution of environmental surveillance programs in a safe and economical way, avoiding unnecessary analysis. (author) [pt

The measure of radiocarbon in the drating of environmental samples

International Nuclear Information System (INIS)

Ruiz Pessenda, L.C.; Camargo, P.B. de

1990-01-01

An analytical system for radiocarbon dating of environmental samples (charcoal, shell, wood, etc.) using low level liquid scintillation spectrometry has been developed and optimized at Center for Nuclear Energy in Agriculture of the University of Sao Paulo. Physical and chemical pretreatment of samples to remove oils, resins, carbonates and fulvic and humic acids; the benzene synthesis of NBS oxalic acid standard, calcium carbonate P.A. and marble and the results of benzene yield; the optimization of radiocarbon counting window; the effect of scintillators PPO-POPOP and butyl PBD on the efficiency of detection and background of radiocarbon, are described. Samples of charcoal, shell and wood, previously dated at the radiocarbon laboratories of Centre des Faibles Radioactives, France, and Instituto de Geociencias of USP, are analysed for preliminary laboratory intercomparison. (author) [pt

Gamma-ray self-attenuation corrections in environmental samples

International Nuclear Information System (INIS)

Robu, E.; Giovani, C.

2009-01-01

Gamma-spectrometry is a commonly used technique in environmental radioactivity monitoring. Frequently the bulk samples that should be measured differ with respect to composition and density from the reference sample used for efficiency calibration. Correction factors should be applied in these cases for activity measurement. Linear attenuation coefficients and self-absorption correction factors have been evaluated for soil, grass and liquid sources with different densities and geometries.(authors)

Evaluating the reproducibility of environmental radioactivity monitoring data through replicate sample analysis

International Nuclear Information System (INIS)

Lindeken, C.L.; White, J.H.; Silver, W.J.

1978-01-01

At the Lawrence Livermore Laboratory, about 10% of the sampling effort in the environmental monitoring program represents replicate sample collection. Replication of field samples was initiated as part of the quality assurance program for environmental monitoring to determine the reproducibility of environmental measurements. In the laboratory these replicates are processed along with routine samples. As all components of variance are included in analysis of such field samples, comparison of the analytical data from replicate analyses provides a basis for estimating the overall reproducibility of the measurements. The replication study indicates that the reproducibility of environmental radioactivity monitoring data is subject to considerably more variability than is indicated by the accompanying counting errors. The data are also compared with analyses of duplicate aliquots from a well mixed sample or with duplicate aliquots of samples with known radionuclide content. These comparisons show that most of the variability is associated with the collection and preparation of the sample rather than with the analytical procedures

Determination of Pu, Am and Cm in Environmental Samples

Energy Technology Data Exchange (ETDEWEB)

Lujaniene, G. [SRI Centre for Physical Sciences and Technology, Vilnius (Lithuania)

2013-07-15

The determination of actinides in the environmental samples at a lower detection limit is required for monitoring purposes and for environmental research. The method for Pu, Am and Cm measurements in soil and sediment samples provides high recoveries and good decontamination from interfering radionuclides. The main steps of the method involve digestion of the samples, separation of radionuclides from matrix using the TOPO /cyclohexane extraction and final purification using extraction Eichrom resins (TEVA, TRU). The accuracy and precision of Pu, Am and Cm analyses were tested using IAEA RM No 135, NIST SRM No 4350b, No 4357 and in intercomparison runs organized by the Riso National Laboratory, Denmark, and in the proficiency tests organized by National Physical Laboratory, UK. The method was applied for measurement of radionuclides in aerosol samples (ashes {approx}30 g), bottom sediments (50-80 g dr. wt) and soil (including Chernobyl soil) samples. (author)

Empirical insights and considerations for the OBT inter-laboratory comparison of environmental samples

International Nuclear Information System (INIS)

Kim, Sang-Bog; Roche, Jennifer

2013-01-01

Organically bound tritium (OBT) is an important tritium species that can be measured in most environmental samples, but has only recently been recognized as a species of tritium in these samples. Currently, OBT is not routinely measured by environmental monitoring laboratories around the world. There are no certified reference materials (CRMs) for environmental samples. Thus, quality assurance (QA), or verification of the accuracy of the OBT measurement, is not possible. Alternatively, quality control (QC), or verification of the precision of the OBT measurement, can be achieved. In the past, there have been differences in OBT analysis results between environmental laboratories. A possible reason for the discrepancies may be differences in analytical methods. Therefore, inter-laboratory OBT comparisons among the environmental laboratories are important and would provide a good opportunity for adopting a reference OBT analytical procedure. Due to the analytical issues, only limited information is available on OBT measurement. Previously conducted OBT inter-laboratory practices are reviewed and the findings are described. Based on our experiences, a few considerations were suggested for the international OBT inter-laboratory comparison exercise to be completed in the near future. -- Highlights: ► Inter-laboratory OBT comparisons would provide a good opportunity for developing reference OBT analytical procedures. ► The measurement of environmental OBT concentrations has a higher associated uncertainty. ► Certified reference materials for OBT in environmental samples are required

Sample preparation of environmental samples using benzene synthesis followed by high-performance LSC

International Nuclear Information System (INIS)

Filippis, S. De; Noakes, J.E.

1991-01-01

Liquid scintillation counting (LSC) techniques have been widely employed as the detection method for determining environmental levels of tritium and 14 C. Since anthropogenic and nonanthropogenic inputs to the environment are a concern, sampling the environment surrounding a nuclear power facility or fuel reprocessing operation requires the collection of many different sample types, including agriculture products, water, biota, aquatic life, soil, and vegetation. These sample types are not suitable for the direct detection of tritium of 14 C for liquid scintillation techniques. Each sample type must be initially prepared in order to obtain the carbon or hydrogen component of interest and present this in a chemical form that is compatible with common chemicals used in scintillation counting applications. Converting the sample of interest to chemically pure benzene as a sample preparation technique has been widely accepted for processing samples for radiocarbon age-dating applications. The synthesized benzene is composed of the carbon or hydrogen atoms from the original sample and is ideal as a solvent for LSC with excellent photo-optical properties. Benzene synthesis followed by low-background scintillation counting can be applied to the preparation and measurement of environmental samples yielding good detection sensitivities, high radionuclide counting efficiency, and shorter preparation time. The method of benzene synthesis provides a unique approach to the preparation of a wide variety of environmental sample types using similar chemistry for all samples

Environmental surveillance master sampling schedule

International Nuclear Information System (INIS)

Bisping, L.E.

1995-02-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest Laboratory (PNL) for the U.S. Department of Energy (DOE). This document contains the planned 1994 schedules for routine collection of samples for the Surface Environmental Surveillance Project (SESP), Drinking Water Project, and Ground-Water Surveillance Project. Samples are routinely collected for the SESP and analyzed to determine the quality of air, surface water, soil, sediment, wildlife, vegetation, foodstuffs, and farm products at Hanford Site and surrounding communities. The responsibility for monitoring onsite drinking water falls outside the scope of the SESP. PNL conducts the drinking water monitoring project concurrent with the SESP to promote efficiency and consistency, utilize expertise developed over the years, and reduce costs associated with management, procedure development, data management, quality control, and reporting. The ground-water sampling schedule identifies ground-water sampling .events used by PNL for environmental surveillance of the Hanford Site. Sampling is indicated as annual, semi-annual, quarterly, or monthly in the sampling schedule. Some samples are collected and analyzed as part of ground-water monitoring and characterization programs at Hanford (e.g. Resources Conservation and Recovery Act (RCRA), Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA), or Operational). The number of samples planned by other programs are identified in the sampling schedule by a number in the analysis column and a project designation in the Cosample column. Well sampling events may be merged to avoid redundancy in cases where sampling is planned by both-environmental surveillance and another program

Environmental surveillance master sampling schedule

Energy Technology Data Exchange (ETDEWEB)

Bisping, L.E.

1995-02-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest Laboratory (PNL) for the U.S. Department of Energy (DOE). This document contains the planned 1994 schedules for routine collection of samples for the Surface Environmental Surveillance Project (SESP), Drinking Water Project, and Ground-Water Surveillance Project. Samples are routinely collected for the SESP and analyzed to determine the quality of air, surface water, soil, sediment, wildlife, vegetation, foodstuffs, and farm products at Hanford Site and surrounding communities. The responsibility for monitoring onsite drinking water falls outside the scope of the SESP. PNL conducts the drinking water monitoring project concurrent with the SESP to promote efficiency and consistency, utilize expertise developed over the years, and reduce costs associated with management, procedure development, data management, quality control, and reporting. The ground-water sampling schedule identifies ground-water sampling .events used by PNL for environmental surveillance of the Hanford Site. Sampling is indicated as annual, semi-annual, quarterly, or monthly in the sampling schedule. Some samples are collected and analyzed as part of ground-water monitoring and characterization programs at Hanford (e.g. Resources Conservation and Recovery Act (RCRA), Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA), or Operational). The number of samples planned by other programs are identified in the sampling schedule by a number in the analysis column and a project designation in the Cosample column. Well sampling events may be merged to avoid redundancy in cases where sampling is planned by both-environmental surveillance and another program.

Measurements of tritium (HTO, TFWT, OBT) in environmental samples at varying distances from a nuclear generating station

Energy Technology Data Exchange (ETDEWEB)

Kotzer, T.G.; Workman, W.J.G

1999-12-01

Concentrations of tritium have been measured in environmental samples (vegetation, water, soil, air) from sites distal and proximal to a CANDU nuclear generating station in Southern Ontario (OPG-Pickering). Levels of tissue-free water tritium (TFWT) and organically bound tritium (OBT) in vegetation are as high as 24,000 TU immediately adjacent to the nuclear generating station and rapidly decrease to levels of tritium which are comparable to natural ambient concentrations for tritium in the environment (approximately {<=} 60 TU). Tritium concentrations (OBT, TFTW) have also been measured in samples of vegetation and tree rings growing substantial distances away from nuclear generating stations and are within a factor of 1 to 2 of the ambient levels of tritium measured in precipitation in several parts of Canada (approximately {<=}30 TU). (author)

Measurements of tritium (HTO, TFWT, OBT) in environmental samples at varying distances from a nuclear generating station

International Nuclear Information System (INIS)

Kotzer, T.G.; Workman, W.J.G.

1999-12-01

Concentrations of tritium have been measured in environmental samples (vegetation, water, soil, air) from sites distal and proximal to a CANDU nuclear generating station in Southern Ontario (OPG-Pickering). Levels of tissue-free water tritium (TFWT) and organically bound tritium (OBT) in vegetation are as high as 24,000 TU immediately adjacent to the nuclear generating station and rapidly decrease to levels of tritium which are comparable to natural ambient concentrations for tritium in the environment (approximately ≤ 60 TU). Tritium concentrations (OBT, TFTW) have also been measured in samples of vegetation and tree rings growing substantial distances away from nuclear generating stations and are within a factor of 1 to 2 of the ambient levels of tritium measured in precipitation in several parts of Canada (approximately ≤30 TU). (author)

Gaseous radiocarbon measurements of small samples

International Nuclear Information System (INIS)

Ruff, M.; Szidat, S.; Gaeggeler, H.W.; Suter, M.; Synal, H.-A.; Wacker, L.

2010-01-01

Radiocarbon dating by means of accelerator mass spectrometry (AMS) is a well-established method for samples containing carbon in the milligram range. However, the measurement of small samples containing less than 50 μg carbon often fails. It is difficult to graphitise these samples and the preparation is prone to contamination. To avoid graphitisation, a solution can be the direct measurement of carbon dioxide. The MICADAS, the smallest accelerator for radiocarbon dating in Zurich, is equipped with a hybrid Cs sputter ion source. It allows the measurement of both, graphite targets and gaseous CO 2 samples, without any rebuilding. This work presents experiences dealing with small samples containing 1-40 μg carbon. 500 unknown samples of different environmental research fields have been measured yet. Most of the samples were measured with the gas ion source. These data are compared with earlier measurements of small graphite samples. The performance of the two different techniques is discussed and main contributions to the blank determined. An analysis of blank and standard data measured within years allowed a quantification of the contamination, which was found to be of the order of 55 ng and 750 ng carbon (50 pMC) for the gaseous and the graphite samples, respectively. For quality control, a number of certified standards were measured using the gas ion source to demonstrate reliability of the data.

Measuring the environmental literacy of teachers | Swanepoel ...

African Journals Online (AJOL)

The crucial role that teachers' environmental literacy plays in realising the goals of environmental education and the importance of the ability, to determine their level of environmental literacy, are argued. A measuring instrument was developed in this regard and was applied to a sample of teachers. An analysis of the results ...

Natural Radioactivity Pattern of Surabaya Water Environmental Samples

International Nuclear Information System (INIS)

Rosidi; Agus Taftazani

2007-01-01

The gross β radioactivity and natural radionuclide of Surabaya environmental samples pattern have been evaluated. The environmental samples were chosen randomly at 12 locations. The environment samples were water (fresh, estuary and coastal), sediment, eichhornia crassipes (Mart) Solms, Mangrove (Rhizophora stylosa), (Moolgarda delicatus) fish and (Johnius (Johnieops) borneensis) (Sharpnose hammer croaker) fish. The water sample was evaporated; the sediment sample was dried and ground; the biotic samples was burnt at the temperature 500 °C ; The gross β measurement using GM detector and the radionuclides has been identified by γ spectrometer. From the investigation results could be concluded that the natural radioactivity of environmental samples was very low. gross-β of water samples were lower than the threshold value of local government regulation of Surabaya no: 2 year 2004 (1 Bq/L). The distribution of gross-β activity of eichhornia crassipes (Mart) Solms was higher than the other biotic, water and sediment samples as well as the accumulation of radionuclides in the water organism was taken place. The result of identification using γ spectrometer has detected 7 of radionuclides, i.e 210 Pb, 212 Pb, 214 Pb, 208 Tl, 214 Bi, 228 Ac, and 40 K in all sample. The distribution factor of sediment F D was less than bioaccumulation factor of biotic F B and it indicates that there the radionuclide accumulation migration follows the pattern of water - sediment - biotic sample. (author)

Application of ICP-MS in Environmental Sampling Analysis for Safeguards

International Nuclear Information System (INIS)

Eko Pudjadi; Petrus Zacharias; Budi Prayitno

2004-01-01

Environmental samples measured by ICP-MS were analyzed for safeguards. There are two isotopes in environmental sampling that is used to find out the origin of nuclear materials and verify undeclared nuclear activities. Uranium isotopes are 234 U, 235 U, 236 U and 238 U and Plutonium isotopes are 239 Pu, 240 Pu, 241 Pu and 242 Pu. Uranium isotopes are used to verify an existing of nuclear power plants, enrichment plants or reprocessing plants. Plutonium isotopes are used to clarify global fallout from nuclear weapon testing and accident of nuclear facility or military purposes. The high sensitivity of ICP-MS can detect the isotopic fingerprint and trace elements in ppb concentration; ICP-MS has been applied to measure 235 U isotopic ratio and 240 Pu/ 239 Pu isotopic ratios. The sensitivity of ICP-MS is high precision and low operational cost in environmental sampling and can be considered in nuclear power design based on safeguards for development countries. (author)

Screening of IAEA environmental samples for fissile material content

International Nuclear Information System (INIS)

Hembree, Doyle M. Jr.; Carter, Joel A.; Devault, Gerald L.; Whitaker, J. Michael; Glasgow, David

2001-01-01

Full text: Analysis of environmental samples for the International Atomic Energy Agency (IAEA) Strengthened Safeguards Systems program requires that stringent measures be taken to control contamination. To facilitate contamination control, it is extremely useful to have some estimate of the fissile content of a given sample prior to beginning sample preparation and analysis. This is particularly true for laboratories that employ clean rooms during sample preparation. A review of the analytical results for samples submitted between January 1, 1999 and September 1, 2000 revealed that the total uranium content values ranged from 0.2 to greater than 500,000 ng/sample. Poor estimates of the uranium or plutonium content in the samples have caused some of the laboratories in the IAEA Network of Analytical Laboratories (NWAL) to experience clean laboratory contamination, sample cross contamination, and non-ideal uranium spike additions. This has led to significant increases in analysis costs (e.g., recertification of clean rooms after removing contamination, and rerunning samples) and degradation in data quality. A number of methods have been proposed for screening environmental samples for fissile material content, including gamma spectrometry, x-ray fluorescence, kinetic phosphorimetry (KPA), and inductively coupled plasma-mass spectrometry (ICP-MS). Gamma spectrometry and x-ray fluorescence are suitable for screening samples with microgram or greater quantities of uranium. ICP-MS and KPA are used successfully in some DOE NWAL laboratories to screen environmental samples. A neutron activation analysis (NAA) method that offers numerous advantages over other screening techniques for environmental samples has recently been proposed. Fissile materials such as 239 Pu and 235 U can be made to undergo fission in the intense neutron field to which they are exposed during neutron activation analysis (NAA). Some of the fission products emit neutrons referred to as 'delayed

Empirical insights and considerations for the OBT inter-laboratory comparison of environmental samples.

Science.gov (United States)

Kim, Sang-Bog; Roche, Jennifer

2013-08-01

Organically bound tritium (OBT) is an important tritium species that can be measured in most environmental samples, but has only recently been recognized as a species of tritium in these samples. Currently, OBT is not routinely measured by environmental monitoring laboratories around the world. There are no certified reference materials (CRMs) for environmental samples. Thus, quality assurance (QA), or verification of the accuracy of the OBT measurement, is not possible. Alternatively, quality control (QC), or verification of the precision of the OBT measurement, can be achieved. In the past, there have been differences in OBT analysis results between environmental laboratories. A possible reason for the discrepancies may be differences in analytical methods. Therefore, inter-laboratory OBT comparisons among the environmental laboratories are important and would provide a good opportunity for adopting a reference OBT analytical procedure. Due to the analytical issues, only limited information is available on OBT measurement. Previously conducted OBT inter-laboratory practices are reviewed and the findings are described. Based on our experiences, a few considerations were suggested for the international OBT inter-laboratory comparison exercise to be completed in the near future. Crown Copyright © 2013. Published by Elsevier Ltd. All rights reserved.

Environmental surveillance master sampling schedule

International Nuclear Information System (INIS)

Bisping, L.E.

1997-01-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest National Laboratory (PNNL)(a) for the US Department of Energy (DOE). This document contains the planned 1997 schedules for routine collection of samples for the Surface Environmental Surveillance Project (SESP) and Drinking Water Monitoring Project. In addition, Section 3.0, Biota, also reflects a rotating collection schedule identifying the year a specific sample is scheduled for collection. The purpose of these monitoring projects is to evaluate levels of radioactive and nonradioactive pollutants in the Hanford environs, as required in DOE Order 5400.1, General Environmental Protection Program, and DOE Order 5400.5, Radiation Protection of the Public and the Environment. The sampling methods will be the same as those described in the Environmental Monitoring Plan, US Department of Energy, Richland Operations Office, DOE/RL91-50, Rev. 1, US Department of Energy, Richland, Washington

An analysis of combined standard uncertainty for radiochemical measurements of environmental samples

International Nuclear Information System (INIS)

Berne, A.

1996-01-01

It is anticipated that future data acquisitions intended for use in radiological risk assessments will require the incorporation of uncertainty analysis. Often, only one aliquot of the sample is taken and a single determination is made. Under these circumstances, the total uncertainty is calculated using the open-quotes propagation of errorsclose quotes approach. However, there is no agreement in the radioanalytical community as to the exact equations to use. The Quality Assurance/Metrology Division of the Environmental Measurements Laboratory has developed a systematic process to compute uncertainties in constituent components of the analytical procedure, as well as the combined standard uncertainty (CSU). The equations for computation are presented here, with examples of their use. They have also been incorporated into a code for use in the spreadsheet application, QuattroPro trademark. Using the spreadsheet with appropriate inputs permits an analysis of the variations in the CSU as a function of several different variables. The relative importance of the open-quotes counting uncertaintyclose quotes can also be ascertained

Soil sampling for environmental contaminants

International Nuclear Information System (INIS)

2004-10-01

The Consultants Meeting on Sampling Strategies, Sampling and Storage of Soil for Environmental Monitoring of Contaminants was organized by the International Atomic Energy Agency to evaluate methods for soil sampling in radionuclide monitoring and heavy metal surveys for identification of punctual contamination (hot particles) in large area surveys and screening experiments. A group of experts was invited by the IAEA to discuss and recommend methods for representative soil sampling for different kinds of environmental issues. The ultimate sinks for all kinds of contaminants dispersed within the natural environment through human activities are sediment and soil. Soil is a particularly difficult matrix for environmental pollution studies as it is generally composed of a multitude of geological and biological materials resulting from weathering and degradation, including particles of different sizes with varying surface and chemical properties. There are so many different soil types categorized according to their content of biological matter, from sandy soils to loam and peat soils, which make analytical characterization even more complicated. Soil sampling for environmental monitoring of pollutants, therefore, is still a matter of debate in the community of soil, environmental and analytical sciences. The scope of the consultants meeting included evaluating existing techniques with regard to their practicability, reliability and applicability to different purposes, developing strategies of representative soil sampling for cases not yet considered by current techniques and recommending validated techniques applicable to laboratories in developing Member States. This TECDOC includes a critical survey of existing approaches and their feasibility to be applied in developing countries. The report is valuable for radioanalytical laboratories in Member States. It would assist them in quality control and accreditation process

Environmental surveillance master sampling schedule

International Nuclear Information System (INIS)

Bisping, L.E.

1994-02-01

This document contains the planned 1994 schedules for routine collection of samples for the Surface Environmental Surveillance Project (SESP), Drinking Water Project, and Ground-Water Surveillance Project. Samples are routinely collected for the SESP and analyzed to determine the quality of air, surface water, soil, sediment, wildlife, vegetation, foodstuffs, and farm products at Hanford Site and surrounding communities. The responsibility for monitoring the onsite drinking water falls outside the scope of the SESP. The Hanford Environmental Health Foundation is responsible for monitoring the nonradiological parameters as defined in the National Drinking Water Standards while PNL conducts the radiological monitoring of the onsite drinking water. PNL conducts the drinking water monitoring project concurrent with the SESP to promote efficiency and consistency, utilize the expertise developed over the years, and reduce costs associated with management, procedure development, data management, quality control and reporting. The ground-water sampling schedule identifies ground-water sampling events used by PNL for environmental surveillance of the Hanford Site

Environmental surveillance master sampling schedule

Energy Technology Data Exchange (ETDEWEB)

Bisping, L.E.

1994-02-01

This document contains the planned 1994 schedules for routine collection of samples for the Surface Environmental Surveillance Project (SESP), Drinking Water Project, and Ground-Water Surveillance Project. Samples are routinely collected for the SESP and analyzed to determine the quality of air, surface water, soil, sediment, wildlife, vegetation, foodstuffs, and farm products at Hanford Site and surrounding communities. The responsibility for monitoring the onsite drinking water falls outside the scope of the SESP. The Hanford Environmental Health Foundation is responsible for monitoring the nonradiological parameters as defined in the National Drinking Water Standards while PNL conducts the radiological monitoring of the onsite drinking water. PNL conducts the drinking water monitoring project concurrent with the SESP to promote efficiency and consistency, utilize the expertise developed over the years, and reduce costs associated with management, procedure development, data management, quality control and reporting. The ground-water sampling schedule identifies ground-water sampling events used by PNL for environmental surveillance of the Hanford Site.

Environmental gamma-ray measurements using in situ and core sampling techniques

International Nuclear Information System (INIS)

Dickson, H.W.; Kerr, G.D.; Perdue, P.T.; Abdullah, S.A.

1976-01-01

Dose rates from natural radionuclides and 137 Cs in soils of the Oak Ridge area have been determined from in situ and core sample measurements. In situ γ-ray measurements were made with a transportable spectrometer. A tape of spectral data and a soil core sample from each site were returned to ORNL for further analysis. Information on soil composition, density and moisture content and on the distribution of cesium in the soil was obtained from the core samples. In situ spectra were analyzed by a computer program which identified and assigned energies to peaks, integrated the areas under the peaks, and calculated radionuclide concentrations based on a uniform distribution in the soil. The assumption of a uniform distribution was adequate only for natural radionuclides, but simple corrections can be made to the computer calculations for man-made radionuclides distributed on the surface or exponentially in the soil. For 137 Cs a correction was used based on an exponential function fitted to the distribution measured in core samples. At typical sites in Oak Ridge, the dose rate determined from these measurements was about 5 μrad/hr. (author)

Fast radiochemical procedure to measure neptunium, plutonium, americium and curium in environmental samples for application in environmental monitoring and in radioecology research

International Nuclear Information System (INIS)

Pimpel, M.; Schuettelkopf, H.

1984-01-01

A radiochemical method is described by which Np, Pu, Am and Cm in environmental samples can be determined. The transuranium elements are dissolved with acids out of the ashed material. Np/Pu is separated from Am/Cm by sequential extraction using TOPO/cyclohexane. The two fractions are radiochemically purified. Np-237, Pu-239+240, Pu-238 and Pu-236 as well as Am-243, Am-241, Cm-244 and Cm-242 are measured by alpha spectrometery. Pu-236, Am-243 and Np-239 are used to determine the respective yields. A fast method of Np-239 preparation is described. The chemical yields range from 60 to 90%. The detection limit attained per nuclide is 10 fCi/sample. 20 reference, 1 table

Intrepretation of work area and environmental sampling

International Nuclear Information System (INIS)

Ritter, P.D.; Alvarez, J.L.; Novick, V.J.

1985-01-01

Meaningful interpretation of widely variable airborne contamination measurements is a difficult problem. Exposure limits, action levels, etc., are rigid interpretations of inherently variable environmental or workplace conditions, and are useful for control and regulatory compliance evaluations. Such limits force actions to reduce contamination, but have limited usefulness as benchmarks for evaluating isolated or nonrepresentative measurements. This paper deals with interpretation of exposure based on nonrepresentative sampling. The use of hard limits for interpreting measurements of legal record simplifies judgment during cursory audits; more aggressive questioning of the validity of these records may effectively invalidate them in a courtroom situation

Method validation and uncertainty evaluation of organically bound tritium analysis in environmental sample.

Science.gov (United States)

Huang, Yan-Jun; Zeng, Fan; Zhang, Bing; Chen, Chao-Feng; Qin, Hong-Juan; Wu, Lian-Sheng; Guo, Gui-Yin; Yang, Li-Tao; Shang-Guan, Zhi-Hong

2014-08-01

The analytical method for organically bound tritium (OBT) was developed in our laboratory. The optimized operating conditions and parameters were established for sample drying, special combustion, distillation, and measurement on a liquid scintillation spectrometer (LSC). Selected types of OBT samples such as rice, corn, rapeseed, fresh lettuce and pork were analyzed for method validation of recovery rate reproducibility, the minimum detection concentration, and the uncertainty for typical low level environmental sample was evaluated. The combustion water recovery rate of different dried environmental sample was kept at about 80%, the minimum detection concentration of OBT ranged from 0.61 to 0.89 Bq/kg (dry weight), depending on the hydrogen content. It showed that this method is suitable for OBT analysis of environmental sample with stable recovery rate, and the combustion water yield of a sample with weight about 40 g would provide sufficient quantity for measurement on LSC. Copyright © 2014 Elsevier Ltd. All rights reserved.

Efficiency corrections in determining the 137Cs inventory of environmental soil samples by using relative measurement method and GEANT4 simulations

International Nuclear Information System (INIS)

Li, Gang; Liang, Yongfei; Xu, Jiayun; Bai, Lixin

2015-01-01

The determination of 137 Cs inventory is widely used to estimate the soil erosion or deposition rate. The generally used method to determine the activity of volumetric samples is the relative measurement method, which employs a calibration standard sample with accurately known activity. This method has great advantages in accuracy and operation only when there is a small difference in elemental composition, sample density and geometry between measuring samples and the calibration standard. Otherwise it needs additional efficiency corrections in the calculating process. The Monte Carlo simulations can handle these correction problems easily with lower financial cost and higher accuracy. This work presents a detailed description to the simulation and calibration procedure for a conventionally used commercial P-type coaxial HPGe detector with cylindrical sample geometry. The effects of sample elemental composition, density and geometry were discussed in detail and calculated in terms of efficiency correction factors. The effect of sample placement was also analyzed, the results indicate that the radioactive nuclides and sample density are not absolutely uniform distributed along the axial direction. At last, a unified binary quadratic functional relationship of efficiency correction factors as a function of sample density and height was obtained by the least square fitting method. This function covers the sample density and height range of 0.8–1.8 g/cm 3 and 3.0–7.25 cm, respectively. The efficiency correction factors calculated by the fitted function are in good agreement with those obtained by the GEANT4 simulations with the determination coefficient value greater than 0.9999. The results obtained in this paper make the above-mentioned relative measurements more accurate and efficient in the routine radioactive analysis of environmental cylindrical soil samples. - Highlights: • Determination of 137 Cs inventory in environmental soil samples by using relative

Analytical Methodology for the Determination of Radium Isotopes in Environmental Samples

International Nuclear Information System (INIS)

2010-01-01

Reliable, comparable and 'fit for purpose' results are an essential requirement for any decision based on analytical measurements. For the analyst, the availability of tested and validated analytical procedures is an extremely important tool for production of such analytical measurements. For maximum utility, such procedures should be comprehensive, clearly formulated, and readily available to both the analyst and the customer for reference. Since 2004, the environment programme of the IAEA has included activities aimed at the development of a set of procedures for the determination of radionuclides in terrestrial environmental samples. Measurements of radium isotopes are important for radiological and environmental protection, geochemical and geochronological investigations, hydrology, etc. The suite of isotopes creates and stimulates continuing interest in the development of new methods for determination of radium in various media. In this publication, the four most routinely used analytical methods for radium determination in biological and environmental samples, i.e. alpha spectrometry, gamma spectrometry, liquid scintillation spectrometry and mass spectrometry, are reviewed

Experience with environmental sampling at gas centrifuge enrichment plants

International Nuclear Information System (INIS)

Ekenstam, G. af; Bush, W.; Janov, J.; Kuhn, E.; Ryjinski, M.

2001-01-01

Environmental sampling has been used routinely by the IAEA since 1996 after the IAEA Board of Governors approved it in March 1995 as a new technique to strengthen safeguards and improve efficiency. In enrichment plants it is used to confirm that there has been no production of highly enriched uranium (HEU), or production of uranium at above the declared enrichment. The use of environmental sampling is based on the assumption that every process, no matter how leak tight, will release small amounts of process material to the environment. Even though these releases of nuclear material are extremely small in gas centrifuge enrichment plants, and well below levels of concern from a health physics and safety standpoint, they are detectable and their analysis provides an indication of the enrichment of the material that has been processed in the plant. The environmental samples at enrichment plants are collected by swiping selected areas of the plant with squares of cotton cloth (10x10 cm) from sampling kits prepared in ultra clean condition. The squares of cotton cloth sealed in plastic bags are sent for analysis to the Network Analytical Laboratories. The analysis includes the measurement of the uranium isotopic composition in uranium-containing particles by Thermal lonization Mass Spectroscopy (TIMS) or Secondary ION Mass Spectroscopy (SIMS). Since the implementation of environmental sampling, swipes have been collected from 240 sampling points at three gas centrifuge plants of URENCO, which have a total throughput of more than 8,000 tonnes of uranium per year. The particle analysis results generally reflected the known operational history of the plants and confirmed that they had only been operated to produce uranium with enrichment less than 5% 235 U. The information about the content of the minor isotopes 234 U and 236 U also indicates that depleted and recycled uranium were sometimes used as feed materials in some plants. An example is given of the TIMS particle

Resonance ionization mass spectrometry system for measurement of environmental samples

International Nuclear Information System (INIS)

Pibida, L.; McMahon, C.A.; Noertershaeuser, W.; Bushaw, B.A.

2002-01-01

A resonance ionization mass spectrometry (RIMS) system has been developed at the National Institute of Standards and Technology (NIST) for sensitive and selective determination of radio-cesium in the environment. The overall efficiency was determined to be 4x10-7 with a combined (laser and mass spectrometer) selectivity of 108 for both 135Cs and 137Cs with respect to 133Cs. RIMS isotopic ratio measurements of 135Cs/ 137Cs were performed on a nuclear fuel burn-up sample and compared to measurements on a similar system at Pacific Northwest National Laboratory (PNNL) and to conventional thermal ionization mass spectrometry (TIMS). Results of preliminary RIMS investigations on a freshwater lake sediment sample are also discussed

The influence of uncertainties of measurements in laboratory performance evaluation by intercomparison program in radionuclide analyses of environmental samples

International Nuclear Information System (INIS)

Tauhata, L.; Vianna, M.E.; Oliveira, A.E. de; Clain, A.F.; Ferreira, A.C.M.; Bernardes, E.M.

2000-01-01

The accuracy and precision of results of the radionuclide analyses in environmental samples are widely claimed internationally due to its consequences in the decision process coupled to evaluation of environmental pollution, impact, internal and external population exposure. These characteristics of measurement of the laboratories can be shown clearly using intercomparison data, due to the existence of a reference value and the need of three determinations for each analysis. In intercomparison studies accuracy in radionuclide assays in low-level environmental samples has usually been the main focus in performance evaluation and it can be estimated by taking into account the deviation between the experimental laboratory mean value and the reference value. The laboratory repeatability of measurements or their standard deviation is seldom included in performance evaluation. In order to show the influence of the uncertainties in performance evaluation of the laboratories, data of 22 intercomparison runs which distributed 790 spiked environmental samples to 20 Brazilian participant laboratories were compared, using the 'Normalised Standard Deviation' as statistical criteria for performance evaluation of U.S.EPA. It mainly takes into account the laboratory accuracy and the performance evaluation using the same data classified by normalised standard deviation modified by a weight reactor that includes the individual laboratory uncertainty. The results show a relative decrease in laboratory performance in each radionuclide assay: 1.8% for 65 Zn, 2.8% for 40 K, 3.4 for 60 Co, 3.7% for 134 Cs, 4.0% for 137 Cs, 4.4% for Th and U nat , 4.5% for 3 H, 6.3% for 133 Ba, 8.6% for 90 Sr, 10.6% for Gross Alpha, 10.9% for 106 Ru, 11.1% for 226 Ra, 11.5% for Gross Beta and 13.6% for 228 Ra. The changes in the parameters of the statistical distribution function were negligible and the distribution remained as Gaussian type for all radionuclides analysed. Data analyses in terms of

Sampling method of environmental radioactivity monitoring

International Nuclear Information System (INIS)

1984-01-01

This manual provides sampling methods of environmental samples of airborne dust, precipitated dust, precipitated water (rain or snow), fresh water, soil, river sediment or lake sediment, discharged water from a nuclear facility, grains, tea, milk, pasture grass, limnetic organisms, daily diet, index organisms, sea water, marine sediment, marine organisms, and that for tritium and radioiodine determination for radiation monitoring from radioactive fallout or radioactivity release by nuclear facilities. This manual aims at the presentation of standard sampling procedures for environmental radioactivity monitoring regardless of monitoring objectives, and shows preservation method of environmental samples acquired at the samplingpoint for radiation counting for those except human body. Sampling techniques adopted in this manual is decided by the criteria that they are suitable for routine monitoring and any special skillfulness is not necessary. Based on the above-mentioned principle, this manual presents outline and aims of sampling, sampling position or object, sampling quantity, apparatus, equipment or vessel for sampling, sampling location, sampling procedures, pretreatment and preparation procedures of a sample for radiation counting, necessary recording items for sampling and sample transportation procedures. Special attention is described in the chapter of tritium and radioiodine because these radionuclides might be lost by the above-mentioned sample preservation method for radiation counting of less volatile radionuclides than tritium or radioiodine. (Takagi, S.)

Fallout Concentration Various Environmental Samples in Indonesia

International Nuclear Information System (INIS)

Sutarman

2001-01-01

The testing of nuclear weapons have been carried out by the advanced countries, such as United States, Russian Federation, United Kingdom, France, China, India and Pakistan, since about 1945 until 1998. Nuclear weapons tests were conducted at various locations, on and above the earth's surface or underground or on and under the ocean's surface. Nuclear explosions caused the radionuclides of fission product, such as 131 l, 89 Sr, 90 Sr, 134 Cs, 137 Cs, and 239 Pu released to the atmospheric layer. In the atmospheric layer, the long-lived radionuclides, i.e, 90 Sr dan 137 Cs will be distributed into the environment as the fallout radionuclides, and deposited in the various environmental samples (soil, water, and biota). In general, at several locations in Indonesia the 90 Sr and 137 Cs in the various environmental samples still can be detected. The data of measurement results of 90 Sr and 137 Cs concentrations were generally lower than that from some countries in the northern hemisphere. (author)

Hanford Site Environmental Surveillance Master Sampling Schedule

International Nuclear Information System (INIS)

Bisping, L.E.

1999-01-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest National Laboratory (PNNL) for the U.S. Department of Energy (DOE). Sampling is conducted to evaluate levels of radioactive and nonradioactive pollutants in the Hanford environs, as required in DOE Order 5400.1, ''General Environmental protection Program,'' and DOE Order 5400.5, ''Radiation Protection of the Public and the Environment.'' The sampling methods are described in the Environmental Monitoring Plan, United States Department of Energy, Richland Operations Office, DOE/RL-91-50, Rev.2, U.S. Department of Energy, Richland, Washington. This document contains the CY1999 schedules for the routine collection of samples for the Surface Environmental Surveillance Project (SESP) and Drinking Water Monitoring Project. Each section includes the sampling location, sample type, and analyses to be performed on the sample. In some cases, samples are scheduled on a rotating basis and may not be collected in 1999 in which case the anticipated year for collection is provided. In addition, a map is included for each media showing approximate sampling locations

Environmental surveillance master sampling schedule

Energy Technology Data Exchange (ETDEWEB)

Bisping, L.E.

1993-01-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest Laboratory (PNL) for the US Department of Energy (DOE). Samples are routinely collected and analyzed to determine the quality of air, surface water, ground water, soil, sediment, wildlife, vegetation, foodstuffs, and farm products at Hanford Site and surrounding communities. This document contains the planned schedule for routine sample collection for the Surface Environmental Surveillance Project (SESP) and Drinking Water Project, and Ground-Water Surveillance Project.

Applications of Liquid-Phase Microextraction in the Sample Preparation of Environmental Solid Samples

Directory of Open Access Journals (Sweden)

Helena Prosen

2014-05-01

Full Text Available Solvent extraction remains one of the fundamental sample preparation techniques in the analysis of environmental solid samples, but organic solvents are toxic and environmentally harmful, therefore one of the possible greening directions is its miniaturization. The present review covers the relevant research from the field of application of microextraction to the sample preparation of environmental solid samples (soil, sediments, sewage sludge, dust etc. published in the last decade. Several innovative liquid-phase microextraction (LPME techniques that have emerged recently have also been applied as an aid in sample preparation of these samples: single-drop microextraction (SDME, hollow fiber-liquid phase microextraction (HF-LPME, dispersive liquid-liquid microextraction (DLLME. Besides the common organic solvents, surfactants and ionic liquids are also used. However, these techniques have to be combined with another technique to release the analytes from the solid sample into an aqueous solution. In the present review, the published methods were categorized into three groups: LPME in combination with a conventional solvent extraction; LPME in combination with an environmentally friendly extraction; LPME without previous extraction. The applicability of these approaches to the sample preparation for the determination of pollutants in solid environmental samples is discussed, with emphasis on their strengths, weak points and environmental impact.

Applications of liquid-phase microextraction in the sample preparation of environmental solid samples.

Science.gov (United States)

Prosen, Helena

2014-05-23

Solvent extraction remains one of the fundamental sample preparation techniques in the analysis of environmental solid samples, but organic solvents are toxic and environmentally harmful, therefore one of the possible greening directions is its miniaturization. The present review covers the relevant research from the field of application of microextraction to the sample preparation of environmental solid samples (soil, sediments, sewage sludge, dust etc.) published in the last decade. Several innovative liquid-phase microextraction (LPME) techniques that have emerged recently have also been applied as an aid in sample preparation of these samples: single-drop microextraction (SDME), hollow fiber-liquid phase microextraction (HF-LPME), dispersive liquid-liquid microextraction (DLLME). Besides the common organic solvents, surfactants and ionic liquids are also used. However, these techniques have to be combined with another technique to release the analytes from the solid sample into an aqueous solution. In the present review, the published methods were categorized into three groups: LPME in combination with a conventional solvent extraction; LPME in combination with an environmentally friendly extraction; LPME without previous extraction. The applicability of these approaches to the sample preparation for the determination of pollutants in solid environmental samples is discussed, with emphasis on their strengths, weak points and environmental impact.

Sorption models and their application in environmental samples

International Nuclear Information System (INIS)

Kamel, Nariman H.M.

2008-01-01

Full text: Naturally occurring radioactive materials (NORM) were found in some environmental soils not high enough to pose problems for human health. The health may be affected by increasing of NORM at some environmental soils. Four soil samples obtained from certain coastal regions in Egypt. Naturally occurring radioactive materials (NORM) of the uranium ( 238 U) series, thorium ( 232 Th) series and the radioactive isotope of potassium ( 40 K) were measured. The soil samples were selected from the situations where the radionuclide concentrations are significantly higher than the average level of other sites. It were chemically analyzed for the uranium, silicon aluminum and iron. The cation exchange capacity (CEC) were determined, it was found lower in the presence of Fe-silicates suggested that Fe-hydroxide had precipitin at the exchangeable edge sites of the clay minerals. The pH of the solid particles at which the net total surface charge is zero was known as the point of zero charge (PZC). The PZC is very important in determining the affinity of the soil samples for different cations and anions. The aim of this work is to determine the natural radiological hazardous of radionuclide at four environmental coastal soil samples in Egypt. The point of zero surface charge was determined using titration tests. Sorption model was developed for this purpose. (author)

A radiochemical procedure for a low-level measurement of ''241Am in environmental samples using a supported functional organo phosphorus extractant

International Nuclear Information System (INIS)

Gasco, C.; Anton, M. P.; Alvarez, A.; Navarro, N.; Salvador, S.

1994-01-01

The transuranides analysis in environmental samples is carried out by CIEMAT using standardized methods based on sequential separation with ionic-exchange resins. The americium fraction is purified through a two-layer ion exchange column and lately in an anion-exchange column in nitric acid methanol medium. The technique is time consuming and the results are not completely satisfactory (low recovery and loss of a-resolution) for some samples. The chemical compound CMPO (octyl(phenyl)-N,N-diisobutyl carbomoylmethyiphosphine oxide) dissolved in TPB (tributyl phosphate) and supported on an inert substrate has been tested directly for ''241Am analysis by a large number of laboratories. A new method that combines both procedures has been developed. The details of the improved procedure are described in this paper. The advantages of its application to environmental samples (urine, faeces and sediments) are discussed. The utilization of standard samples, with americium certified concentrations confirms the reliability of our measurements. (Author) 8 refs

Environmental Measurements Laboratory (EML) procedures manual

International Nuclear Information System (INIS)

Chieco, N.A.; Bogen, D.C.; Knutson, E.O.

1990-11-01

Volume 1 of this manual documents the procedures and existing technology that are currently used by the Environmental Measurements Laboratory. A section devoted to quality assurance has been included. These procedures have been updated and revised and new procedures have been added. They include: sampling; radiation measurements; analytical chemistry; radionuclide data; special facilities; and specifications. 228 refs., 62 figs., 37 tabs. (FL)

Concentration and speciation of radionuclides in environmental samples

International Nuclear Information System (INIS)

Testa, C.; Desideri, D.; Meli, M.A.; Roselli, C.

2000-01-01

The paper will describe three examples dealing with the measure of some natural (U, Th, 2 10Pb, 4 0K) and artificial ( 1 37Cs, 9 0Sr, 2 39 +2 40Pu, 2 41Am) radionuclides in environmental samples such as mosses, sediments, soils. Extraction chromatography, liquid extraction, selective precipitation and electroplating were used to isolate the radionuclides, except for gamma emitters which were detected by gamma spectrometry. Alpha spectrometry were used to measure the alpha emitters and low background beta detector to measure the beta emitters

Nuclear analytical techniques and their application to environmental samples

International Nuclear Information System (INIS)

Lieser, K.H.

1986-01-01

A survey is given on nuclear analytical techniques and their application to environmental samples. Measurement of the inherent radioactivity of elements or radionuclides allows determination of natural radioelements (e.g. Ra), man-made radioelements (e.g. Pu) and radionuclides in the environment. Activation analysis, in particular instrumental neutron activation analysis, is a very reliable and sensitive method for determination of a great number of trace elements in environmental samples, because the most abundant main constituents are not activated. Tracer techniques are very useful for studies of the behaviour and of chemical reactions of trace elements and compounds in the environment. Radioactive sources are mainly applied for excitation of characteristic X-rays (X-ray fluorescence analysis). (author)

Applications of Liquid-Phase Microextraction in the Sample Preparation of Environmental Solid Samples

OpenAIRE

Helena Prosen

2014-01-01

Solvent extraction remains one of the fundamental sample preparation techniques in the analysis of environmental solid samples, but organic solvents are toxic and environmentally harmful, therefore one of the possible greening directions is its miniaturization. The present review covers the relevant research from the field of application of microextraction to the sample preparation of environmental solid samples (soil, sediments, sewage sludge, dust etc.) published in the last decade. Several...

Hanford Site Environmental Surveillance Master Sampling Schedule

International Nuclear Information System (INIS)

Bisping, L.E.

2000-01-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest National Laboratory (PNNL) for the U.S. Department of Energy (DOE). Sampling is conducted to evaluate levels of radioactive and nonradioactive pollutants in the Hanford environs, as required in DOE Order 5400.1, General Environmental Protection Program: and DOE Order 5400.5, Radiation Protection of the Public and the Environment. The sampling design is described in the Operations Office, Environmental Monitoring Plan, United States Department of Energy, Richland DOE/RL-91-50, Rev.2, U.S. Department of Energy, Richland, Washington. This document contains the CY 2000 schedules for the routine collection of samples for the Surface Environmental Surveillance Project (SESP) and Drinking Water Monitoring Project. Each section includes sampling locations, sample types, and analyses to be performed. In some cases, samples are scheduled on a rotating basis and may not be collected in 2000 in which case the anticipated year for collection is provided. In addition, a map showing approximate sampling locations is included for each media scheduled for collection

A practical method for determining γ-ray full-energy peak efficiency considering coincidence-summing and self-absorption corrections for the measurement of environmental samples after the Fukushima reactor accident

Energy Technology Data Exchange (ETDEWEB)

Shizuma, Kiyoshi, E-mail: shizuma@hiroshima-u.ac.jp [Graduate School of Engineering, Hiroshima University, Higashi-Hiroshima 739-8527 (Japan); Oba, Yurika; Takada, Momo [Graduate School of Integrated Arts and Sciences, Hiroshima University, Higashi-Hiroshima 739-8521 (Japan)

2016-09-15

A method for determining the γ-ray full-energy peak efficiency at positions close to three Ge detectors and at the well port of a well-type detector was developed for measuring environmental volume samples containing {sup 137}Cs, {sup 134}Cs and {sup 40}K. The efficiency was estimated by considering two correction factors: coincidence-summing and self-absorption corrections. The coincidence-summing correction for a cascade transition nuclide was estimated by an experimental method involving measuring a sample at the far and close positions of a detector. The derived coincidence-summing correction factors were compared with those of analytical and Monte Carlo simulation methods and good agreements were obtained. Differences in the matrix of the calibration source and the environmental sample resulted in an increase or decrease of the full-energy peak counts due to the self-absorption of γ-rays in the sample. The correction factor was derived as a function of the densities of several matrix materials. The present method was applied to the measurement of environmental samples and also low-level radioactivity measurements of water samples using the well-type detector.

A simple method of correcting for variation of sample thickness in the determination of the activity of environmental samples by gamma spectrometry

International Nuclear Information System (INIS)

Galloway, R.B.

1991-01-01

Gamma ray spectrometry is a well established method of determining the activity of radioactive components in environmental samples. It is usual to maintain precisely the same counting geometry in measurements on samples under investigation as in the calibration measurements on standard materials of known activity, thus avoiding perceived uncertainties and complications in correcting for changes in counting geometry. However this may not always be convenient if, as on some occasions, only a small quantity of sample material is available for analysis. A procedure which avoids re-calibration for each sample size is described and is shown to be simple to use without significantly reducing the accuracy of measurement of the activity of typical environmental samples. The correction procedure relates to the use of cylindrical samples at a constant distance from the detector, the samples all having the same diameter but various thicknesses being permissible. (author)

Hanford site environmental surveillance master sampling schedule

International Nuclear Information System (INIS)

Bisping, L.E.

1998-01-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest National Laboratory (PNNL) for the U.S. Department of Energy (DOE). Sampling is conducted to evaluate levels of radioactive and nonradioactive pollutants in the Hanford environs, as required in DOE Order 5400.1 open-quotes General Environmental Protection Program,close quotes and DOE Order 5400.5, open-quotes Radiation Protection of the Public and the Environment.close quotes The sampling methods are described in the Environmental Monitoring Plan, United States Department of Energy, Richland Operations Office, DOE/RL91-50, Rev. 2, U.S. Department of Energy, Richland, Washington. This document contains the 1998 schedules for routine collection of samples for the Surface Environmental Surveillance Project (SESP) and Drinking Water Monitoring Project. Each section of this document describes the planned sampling schedule for a specific media (air, surface water, biota, soil and vegetation, sediment, and external radiation). Each section includes the sample location, sample type, and analyses to be performed on the sample. In some cases, samples are scheduled on a rotating basis and may not be planned for 1998 in which case the anticipated year for collection is provided. In addition, a map is included for each media showing sample locations

Determination of plutonium isotopes (238Pu, 239Pu, 240Pu, 241Pu) in environmental samples using radiochemical separation combined with radiometric and mass spectrometric measurements.

Science.gov (United States)

Xu, Yihong; Qiao, Jixin; Hou, Xiaolin; Pan, Shaoming; Roos, Per

2014-02-01

This paper reports an analytical method for the determination of plutonium isotopes ((238)Pu, (239)Pu, (240)Pu, (241)Pu) in environmental samples using anion exchange chromatography in combination with extraction chromatography for chemical separation of Pu. Both radiometric methods (liquid scintillation counting and alpha spectrometry) and inductively coupled plasma mass spectrometry (ICP-MS) were applied for the measurement of plutonium isotopes. The decontamination factors for uranium were significantly improved up to 7.5 × 10(5) for 20 g soil compared to the level reported in the literature, this is critical for the measurement of plutonium isotopes using mass spectrometric technique. Although the chemical yield of Pu in the entire procedure is about 55%, the analytical results of IAEA soil 6 and IAEA-367 in this work are in a good agreement with the values reported in the literature or reference values, revealing that the developed method for plutonium determination in environmental samples is reliable. The measurement results of (239+240)Pu by alpha spectrometry agreed very well with the sum of (239)Pu and (240)Pu measured by ICP-MS. ICP-MS can not only measure (239)Pu and (240)Pu separately but also (241)Pu. However, it is impossible to measure (238)Pu using ICP-MS in environmental samples even a decontamination factor as high as 10(6) for uranium was obtained by chemical separation. © 2013 Elsevier B.V. All rights reserved.

Tritium sampling and measurement

International Nuclear Information System (INIS)

Wood, M.J.; McElroy, R.G.; Surette, R.A.; Brown, R.M.

1993-01-01

Current methods for sampling and measuring tritium are described. Although the basic techniques have not changed significantly over the last 10 y, there have been several notable improvements in tritium measurement instrumentation. The design and quality of commercial ion-chamber-based and gas-flow-proportional-counter-based tritium monitors for tritium-in-air have improved, an indirect result of fusion-related research in the 1980s. For tritium-in-water analysis, commercial low-level liquid scintillation spectrometers capable of detecting tritium-in-water concentrations as low as 0.65 Bq L-1 for counting times of 500 min are available. The most sensitive method for tritium-in-water analysis is still 3He mass spectrometry. Concentrations as low as 0.35 mBq L-1 can be detected with current equipment. Passive tritium-oxide-in-air samplers are now being used for workplace monitoring and even in some environmental sampling applications. The reliability, convenience, and low cost of passive tritium-oxide-in-air samplers make them attractive options for many monitoring applications. Airflow proportional counters currently under development look promising for measuring tritium-in-air in the presence of high gamma and/or noble gas backgrounds. However, these detectors are currently limited by their poor performance in humidities over 30%. 133 refs

Environmental surveillance master sampling schedule

International Nuclear Information System (INIS)

Bisping, L.E.

1991-01-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest Laboratory (PNL) for the US Department of Energy (DOE). This document contains the planned schedule for routine sample collection for the Surface Environmental Surveillance Project (SESP) and Ground-Water Monitoring Project. The routine sampling plan for the SESP has been revised this year to reflect changing site operations and priorities. Some sampling previously performed at least annually has been reduced in frequency, and some new sampling to be performed at a less than annual frequency has been added. Therefore, the SESP schedule reflects sampling to be conducted in calendar year 1991 as well as future years. The ground-water sampling schedule is for 1991. This schedule is subject to modification during the year in response to changes in Site operation, program requirements, and the nature of the observed results. Operational limitations such as weather, mechanical failures, sample availability, etc., may also require schedule modifications. Changes will be documented in the respective project files, but this plan will not be reissued. The purpose of these monitoring projects is to evaluate levels of radioactive and nonradioactive pollutants in the Hanford evirons

Environmental surveillance master sampling schedule

Energy Technology Data Exchange (ETDEWEB)

Bisping, L.E.

1991-01-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest Laboratory (PNL) for the US Department of Energy (DOE). This document contains the planned schedule for routine sample collection for the Surface Environmental Surveillance Project (SESP) and Ground-Water Monitoring Project. The routine sampling plan for the SESP has been revised this year to reflect changing site operations and priorities. Some sampling previously performed at least annually has been reduced in frequency, and some new sampling to be performed at a less than annual frequency has been added. Therefore, the SESP schedule reflects sampling to be conducted in calendar year 1991 as well as future years. The ground-water sampling schedule is for 1991. This schedule is subject to modification during the year in response to changes in Site operation, program requirements, and the nature of the observed results. Operational limitations such as weather, mechanical failures, sample availability, etc., may also require schedule modifications. Changes will be documented in the respective project files, but this plan will not be reissued. The purpose of these monitoring projects is to evaluate levels of radioactive and nonradioactive pollutants in the Hanford evirons.

GY SAMPLING THEORY IN ENVIRONMENTAL STUDIES 2: SUBSAMPLING ERROR MEASUREMENTS

Science.gov (United States)

Sampling can be a significant source of error in the measurement process. The characterization and cleanup of hazardous waste sites require data that meet site-specific levels of acceptable quality if scientifically supportable decisions are to be made. In support of this effort,...

Environmental radioactivity measurements Using a compton suppression spectrometer

International Nuclear Information System (INIS)

Sharshar, T.; Elnimr, T.

1998-01-01

The natural and artificial radioactivities of some environmental samples such as soil and vegetables have been studied through gamma-ray spectroscopy with a new constructed compton suppression spectrometer (CSS). The spectrometer consists of a 10% p-type HPGe detector as a main detector, an annular NE-102 A plastic scintillator as a guard detector, and a fast-slow coincidence system employing standard electronic modules for anti-compton operation. This study shows that CSS is a powerful tool for measuring the low level activities of environmental samples

A radiochemical procedure for a low-level measurement of ''241 Am in environmental samples using a supported functional organo phosphorus extractant

International Nuclear Information System (INIS)

Gasco, C.; Anton, M.A.; Alvarez, A.; Navarro, N.; Salvador, S.

1994-01-01

The transuranides analysis in environmental samples is carried out by CIEMAT using standardized methods based on sequential separation with ionic-exchange resins. The americium fraction is purified through a two-layer ion exchange column and lately in an anion-exchange column in nitric acid methanol medium. The technique is time-consuming and the results are not completely satisfactory (low recovery and loss of alpha-resolution) for some samples. The chemical compound CMPO (octyl(phenyl).N,N-diisobutyl carbomoylmethyiphosphine oxide) dissolved in TPB (tributyl phosphate) and supported on an inert substrate has been tested directly for ''241 Am analysis by a large number of laboratories. A new method that combines both procedures has been developed. The details of the improved procedure are described in this paper. The advantages of its application to environmental samples (urine, faeces and sediments) are discussed. The utilization of standard, with americium certified concentrations confirms the reliability of our measurements

DOE methods for evaluating environmental and waste management samples

Energy Technology Data Exchange (ETDEWEB)

Goheen, S.C.; McCulloch, M.; Thomas, B.L.; Riley, R.G.; Sklarew, D.S.; Mong, G.M.; Fadeff, S.K. [eds.

1994-10-01

DOE Methods for Evaluating Environmental and Waste Management Samples (DOE Methods) is a resource intended to support sampling and analytical activities for the evaluation of environmental and waste management samples from U.S. Department of Energy (DOE) sites. DOE Methods is the result of extensive cooperation from all DOE analytical laboratories. All of these laboratories have contributed key information and provided technical reviews as well as significant moral support leading to the success of this document. DOE Methods is designed to encompass methods for collecting representative samples and for determining the radioisotope activity and organic and inorganic composition of a sample. These determinations will aid in defining the type and breadth of contamination and thus determine the extent of environmental restoration or waste management actions needed, as defined by the DOE, the U.S. Environmental Protection Agency, or others. The development of DOE Methods is supported by the Analytical Services Division of DOE. Unique methods or methods consolidated from similar procedures in the DOE Procedures Database are selected for potential inclusion in this document. Initial selection is based largely on DOE needs and procedure applicability and completeness. Methods appearing in this document are one of two types, {open_quotes}Draft{close_quotes} or {open_quotes}Verified{close_quotes}. {open_quotes}Draft{close_quotes} methods that have been reviewed internally and show potential for eventual verification are included in this document, but they have not been reviewed externally, and their precision and bias may not be known. {open_quotes}Verified{close_quotes} methods in DOE Methods have been reviewed by volunteers from various DOE sites and private corporations. These methods have delineated measures of precision and accuracy.

DOE methods for evaluating environmental and waste management samples

International Nuclear Information System (INIS)

Goheen, S.C.; McCulloch, M.; Thomas, B.L.; Riley, R.G.; Sklarew, D.S.; Mong, G.M.; Fadeff, S.K.

1994-10-01

DOE Methods for Evaluating Environmental and Waste Management Samples (DOE Methods) is a resource intended to support sampling and analytical activities for the evaluation of environmental and waste management samples from U.S. Department of Energy (DOE) sites. DOE Methods is the result of extensive cooperation from all DOE analytical laboratories. All of these laboratories have contributed key information and provided technical reviews as well as significant moral support leading to the success of this document. DOE Methods is designed to encompass methods for collecting representative samples and for determining the radioisotope activity and organic and inorganic composition of a sample. These determinations will aid in defining the type and breadth of contamination and thus determine the extent of environmental restoration or waste management actions needed, as defined by the DOE, the U.S. Environmental Protection Agency, or others. The development of DOE Methods is supported by the Analytical Services Division of DOE. Unique methods or methods consolidated from similar procedures in the DOE Procedures Database are selected for potential inclusion in this document. Initial selection is based largely on DOE needs and procedure applicability and completeness. Methods appearing in this document are one of two types, open-quotes Draftclose quotes or open-quotes Verifiedclose quotes. open-quotes Draftclose quotes methods that have been reviewed internally and show potential for eventual verification are included in this document, but they have not been reviewed externally, and their precision and bias may not be known. open-quotes Verifiedclose quotes methods in DOE Methods have been reviewed by volunteers from various DOE sites and private corporations. These methods have delineated measures of precision and accuracy

Tritium analysis in environmental samples around Nuclear Power Plants and nationwide surveillance of radionuclides in some environmental samples(meat and drinking water)

Energy Technology Data Exchange (ETDEWEB)

Cho, Yong Woo; Han, Man Jung; Cho, Seong Won; Cho, Hong Jun; Oh, Hyeon Kyun; Lee, Jeong Min; Chang, Jae Sook [KORTIC, Taejon (Korea, Republic of)

2001-12-15

12 kind of environmental samples such as soil, underground water, seawater, etc. around the Nuclear Power Plants(NPP) and surface seawater around the Korea peninsula were sampled, For the samples of rain, pine-needle, air, seawater, underground water, chinese cabbage, grain of rice and milk sampled around NPP, and surface seawater and rain sampled all around country, tritium concentration was measured, The tritium concentration in the tap water and the gamma activity in the domestic and imported beef that were sampled at ward in the large city in Korea(Seoul, Pusan, Taegu, Taejun, Inchun, Kwangju) were analyzed for the meat and drinking waters. As the results of analyzing, tritium concentration in rain and tap water were very low all around country, but a little higher around the NPP than general surrounding. At the Wolsung NPP, tritium concentration was descend according to distance from the stack. Tritium activity of surface seawater around the Korea peninsula was also, very low. The measured radioactive elements in the beef is the same as the radioactive elements on the earth surface.

Sample preparation method for ICP-MS measurement of 99Tc in a large amount of environmental samples

International Nuclear Information System (INIS)

Kondo, M.; Seki, R.

2002-01-01

Sample preparation for measurement of 99 Tc in a large amount of soil and water samples by ICP-MS has been developed using 95m Tc as a yield tracer. This method is based on the conventional method for a small amount of soil samples using incineration, acid digestion, extraction chromatography (TEVA resin) and ICP-MS measurement. Preliminary concentration of Tc has been introduced by co-precipitation with ferric oxide. The matrix materials in a large amount of samples were more sufficiently removed with keeping the high recovery of Tc than previous method. The recovery of Tc was 70-80% for 100 g soil samples and 60-70% for 500 g of soil and 500 L of water samples. The detection limit of this method was evaluated as 0.054 mBq/kg in 500 g soil and 0.032 μBq/L in 500 L water. The determined value of 99 Tc in the IAEA-375 (soil sample collected near the Chernobyl Nuclear Reactor) was 0.25 ± 0.02 Bq/kg. (author)

Determination of 90Sr in environmental samples by microwave assisted digestion - chromatographic separation

International Nuclear Information System (INIS)

Torres, J.M.; Llaurado, M.; Rauret, G.

1998-01-01

The stages involved in the determination of 90 Sr in environmental samples are: sample attack, radiochemical separation (of both 90 Sr and its progeny 90 Y) and measurement. For the determination of 90 Sr, the introduction of microwave-assisted digestion methods has improved acid attack by drastically decreasing both digestion time and the volume of acidic reagents. Recent studies describe many applications of microwave-assisted methods for the determination of inorganic and organometallic compounds in several matrices. We have recently studied the microwave-assisted digestion of soils for the 90 Sr determination. The presented work extends the application of microwaves for the 90 Sr determination to other environmental samples such as sediments, vegetation and milk. An open-focused microwave system, which accepts large samples intakes usually required for radioanalytical chemistry due to the low level content of radionuclides in environmental samples, was used. This system can handle up to 10 g of sample intake which, in many cases, is enough to have acceptable limits of detection. Different digestion procedures are optimised for each matrix studied, paying special attention to the microwave power, the time of digestion and the volume of acidic reagents. Once the sample is in solution a new separation procedure using a specific resin -Sr.Spec- is applied and the measurement is performed by liquid scintillation. The results obtained are compared with a previously optimised method based on liquid-liquid extraction of 90 Y and Cerenkov radiation measurement

The procedures manual of the Environmental Measurements Laboratory. Volume 2, 28. edition

Energy Technology Data Exchange (ETDEWEB)

Chieco, N.A. [ed.

1997-02-01

This report contains environmental sampling and analytical chemistry procedures that are performed by the Environmental Measurements Laboratory. The purpose of environmental sampling and analysis is to obtain data that describe a particular site at a specific point in time from which an evaluation can be made as a basis for possible action.

Development of environmental sample analysis techniques for safeguards

International Nuclear Information System (INIS)

Magara, Masaaki; Hanzawa, Yukiko; Esaka, Fumitaka

1999-01-01

JAERI has been developing environmental sample analysis techniques for safeguards and preparing a clean chemistry laboratory with clean rooms. Methods to be developed are a bulk analysis and a particle analysis. In the bulk analysis, Inductively-Coupled Plasma Mass Spectrometer or Thermal Ionization Mass Spectrometer are used to measure nuclear materials after chemical treatment of sample. In the particle analysis, Electron Probe Micro Analyzer and Secondary Ion Mass Spectrometer are used for elemental analysis and isotopic analysis, respectively. The design of the clean chemistry laboratory has been carried out and construction will be completed by the end of March, 2001. (author)

Determination of 241Am and 244Cm in environmental samples

International Nuclear Information System (INIS)

Bonino, N.O.; Grinman, A.D.R.; Serdeiro, N.H.

1998-01-01

The present technique describes a method to separate, purify and measure low levels of americium and curium in different environmental samples such as sediments, soils, water, vegetables, and air filters. The determination of radionuclides in theses environmental matrices have analytical problems, since a simple method doesn't exist for the purification, which is indispensable for its later measuring alpha spectrometry. The developed technique consist on taking an aliquot of the sample to analyze, to add tracer as americium 243 and curium 242, and to dissolve the matrix in a such way to have a clear solution. For the isolation of the americium and curium of the other actinides ar used as separation techniques: precipitation with Fe 3+ , anionic and cationic exchange, and extraction with a appropriate organic solvent. The purification of the americium and curium is followed by the electrodeposition habitually used. The measurement is carried out by alpha spectrometry with a detector of implanted ion. The detection limit for this techniques is of 0,002 Bq/l or 0,2 mBq in the case of filters. (author)

Measurement of environmental radioactivity in Toki district

International Nuclear Information System (INIS)

1981-11-01

When the Institute of Plasma Physics, Nagoya University, expressed the hope to move into Toki district, the environmental problems accompanying the movement were discussed. The effect of the radioactivity leaking from the nuclear facility on human bodies must be far smaller than that of natural radiation, and for the purpose, the amount and fluctuation range of the natural radiation in the district must be known. The initial objectives of this cooperative research were to study on environmental radiation and to make a Geiger counter for the measurement. In 1981, a scintillation counter will be completed, and using a multi-channel pulse height analyzer, the nuclides which are the source of environmental radiation emission will be identified, and the tritium in natural water will be detected. Thus, the evaluation of environmental radiation can be carried out, and the situation before the movement of the research facility can be grasped. In this paper, the natural radioactivity in earth, atmosphere and water and cosmic ray, artificial radioactivity, and environmental radiation exposure dose are reported. Also, the manufacture of a GM counter measuring instrument and the measurements of cosmic ray background, typical earth samples and environmental radioactivity with the GM counter are reported. The related data are attached. (Kako, I.)

Measurement of curium in marine samples

Science.gov (United States)

Schneider, D. L.; Livingston, H. D.

1984-06-01

Measurement of environmentally small but detectable amounts of curium requires reliable, accureate, and sensitive analytical methods. The radiochemical separation developed at Woods Hole is briefly reviewed with specific reference to radiochemical interferences in the alpha spectrometric measurement of curium nuclides and to the relative amounts of interferences expected in different oceanic regimes and sample types. Detection limits for 242 Cm and 244 Cm are ultimately limited by their presence in the 243Am used as curium yield monitor. Environmental standard reference materials are evaluated with regard to curium. The marine literature is reviewed and curium measurements are discussed in relation to their source of introduction to the environment. Sources include ocean dumping of low-level radioactive wastes and discharges from nuclear fuel reporcessing activities, In particular, the question of a detectable presence of 244Cm in global fallout from nuclear weapons testing is addressed and shown to be essentially negligible. Analyses of Scottish coastal sedimantes show traces of 242Cm and 244Cm activity which are believed to originate from transport from sources in the Irish Sea.

An Environmentally Friendly, Cost-Effective Determination of Lead in Environmental Samples Using Anodic Stripping Voltammetry

Science.gov (United States)

Goldcamp, Michael J.; Underwood, Melinda N.; Cloud, Joshua L.; Harshman, Sean

2008-01-01

Contamination of the environment with heavy metals such as lead presents many health risks. Simple, effective, and field-portable methods for the measurement of toxic metals in environmental samples are vital tools for evaluating the risks that these contaminants pose. This article describes the use of new developments in anodic stripping…

Hanford Environmental Monitoring Program schedule for samples, analyses, and measurements for calendar year 1985

International Nuclear Information System (INIS)

Blumer, P.J.; Price, K.R.; Eddy, P.A.; Carlile, J.M.V.

1984-12-01

This report provides the CY 1985 schedule of data collection for the routine Hanford Surface Environmental Monitoring and Ground-Water Monitoring Programs at the Hanford Site. The purpose is to evaluate and report the levels of radioactive and nonradioactive pollutants in the Hanford environs, as required in DOE Order 5484.1. The routine sampling schedule provided herein does not include samples scheduled to be collected during FY 1985 in support of special studies, special contractor support programs, or for quality control purposes. In addition, the routine program outlined in this schedule is subject to modification during the year in response to changes in site operations, program requirements, or unusual sample results

Helium-3 mass spectrometry for low-level tritium analysis of environmental samples

International Nuclear Information System (INIS)

Surano, K.A.; Hudson, G.B.; Failor, R.A.; Sims, J.M.; Holland, R.C.; MacLean, S.C.; Garrison, J.C.

1991-04-01

Helium-3 ( 3 He) mass spectrometry for the analysis of low-level tritium ( 3 H) concentrations in environmental sample matrices was compared with conventional low-level β-decay counting methods. The mass-spectrometry method compared favorably, equaling or surpassing conventional decay-counting methods with respect to most criteria. Additional research and method refinements may make 3 He mass spectrometry the method of choice for routine, low-level to very-low-level 3 H measurements in a wide variety of environmental samples in the future

DOE methods for evaluating environmental and waste management samples

International Nuclear Information System (INIS)

Goheen, S.C.; McCulloch, M.; Thomas, B.L.; Riley, R.G.; Sklarew, D.S.; Mong, G.M.; Fadeff, S.K.

1993-03-01

DOE Methods for Evaluating Environmental and Waste Management Samples (DOE Methods) provides applicable methods in use by. the US Department of Energy (DOE) laboratories for sampling and analyzing constituents of waste and environmental samples. The development of DOE Methods is supported by the Laboratory Management Division (LMD) of the DOE. This document contains chapters and methods that are proposed for use in evaluating components of DOE environmental and waste management samples. DOE Methods is a resource intended to support sampling and analytical activities that will aid in defining the type and breadth of contamination and thus determine the extent of environmental restoration or waste management actions needed, as defined by the DOE, the US Environmental Protection Agency (EPA), or others

DOE methods for evaluating environmental and waste management samples.

Energy Technology Data Exchange (ETDEWEB)

Goheen, S C; McCulloch, M; Thomas, B L; Riley, R G; Sklarew, D S; Mong, G M; Fadeff, S K [eds.; Pacific Northwest Lab., Richland, WA (United States)

1994-04-01

DOE Methods for Evaluating Environmental and Waste Management Samples (DOE Methods) provides applicable methods in use by. the US Department of Energy (DOE) laboratories for sampling and analyzing constituents of waste and environmental samples. The development of DOE Methods is supported by the Laboratory Management Division (LMD) of the DOE. This document contains chapters and methods that are proposed for use in evaluating components of DOE environmental and waste management samples. DOE Methods is a resource intended to support sampling and analytical activities that will aid in defining the type and breadth of contamination and thus determine the extent of environmental restoration or waste management actions needed, as defined by the DOE, the US Environmental Protection Agency (EPA), or others.

Methodology of testing environmental samples from the area surrounding radioactive waste deposits

International Nuclear Information System (INIS)

Kropikova, S.; Pastuchova, D.

1979-01-01

Methods are described of environmental sample investigation in the area surrounding radioactive waste deposits, namely monitoring ground water, surface water, sediments, water flows and catchments, vegetation and soil. Methods of sample preparation, and methods of radionuclides determination in mixtures are also discussed, as are spot activity measurement methods. (author)

Measurement of the tritium concentration in the fractionated distillate from environmental water samples.

Science.gov (United States)

Atkinson, Robert; Eddy, Teresa; Kuhne, Wendy; Jannik, Tim; Brandl, Alexander

2014-09-01

Standard procedures for the measurement of tritium in water samples often require distillation of an appropriate sample aliquot. This distillation process may result in a fractionation of tritiated water and regular light water due to the vapor pressure isotope effect, introducing either a bias or an additional contribution to the total tritium measurement uncertainty. The current study investigates the relative change in vapor pressure isotope effect in the course of the distillation process, distinguishing it from and extending previously published measurements. The separation factor as a quantitative measure of the vapor pressure isotope effect is found to assume values of 1.04 ± 0.036, 1.05 ± 0.026, and 1.07 ± 0.038, depending on the vigor of the boiling process during distillation of the sample. A lower heat setting in the experimental setup, and therefore a less vigorous boiling process, results in a larger value for the separation factor. For a tritium measurement in water samples where the first 5 mL are discarded, the tritium concentration could be underestimated by 4-7%. Copyright © 2014 Elsevier Ltd. All rights reserved.

The uses of neutron capture γ-rays in environmental pollution measurements

International Nuclear Information System (INIS)

Abdel-Haleem, A.S.; Abdel-Samad, M.A.; Zaghloul, R.A.; Hassan, A.M.

1996-01-01

A neutron capture γ-ray spectroscopy facility using an isotopic neutron source, 252 Cf, has been installed and used for investigation of some environmental samples. The facility is designed and calibrated for measurement of the prompt γ-ray spectra due to thermal neutron capture. Qualitative analysis studies of some local environmental samples have been carried out using some developed analytical programs. The experimental results of the environmental pollutant analysis are discussed. (author)

A semi-empirical approach to calculate gamma activities in environmental samples

International Nuclear Information System (INIS)

Palacios, D.; Barros, H.; Alfonso, J.; Perez, K.; Trujillo, M.; Losada, M.

2006-01-01

We propose a semi-empirical method to calculate radionuclide concentrations in environmental samples without the use of reference material and avoiding the typical complexity of Monte-Carlo codes. The calculation of total efficiencies was carried out from a relative efficiency curve (obtained from the gamma spectra data), and the geometric (simulated by Monte-Carlo), absorption, sample and intrinsic efficiencies at energies between 130 and 3000 keV. The absorption and sample efficiencies were determined from the mass absorption coefficients, obtained by the web program XCOM. Deviations between computed results and measured efficiencies for the RGTh-1 reference material are mostly within 10%. Radionuclide activities in marine sediment samples calculated by the proposed method and by the experimental relative method were in satisfactory agreement. The developed method can be used for routine environmental monitoring when efficiency uncertainties of 10% can be sufficient.(Author)

The Development of Low-Level Measurement Capabilities for Total and Isotopic Uranium in Environmental Samples at Brazilian and Argentine Laboratories by ABACC

International Nuclear Information System (INIS)

Guidicini, Olga M.; Olsen, Khris B.; Hembree, Doyle M.; Carter, Joel A.; Whitaker, Michael; Hayes, Susan M.

2005-01-01

accurately measuring both the quantity and isotopic composition of uranium at the levels expected in typical environmental samples (i.e., nanogram quantities).

Quantification of uncertainty in gamma spectrometric analysis of food and environmental samples

International Nuclear Information System (INIS)

Yii Mei Wo; Zaharudin Ahmad; Norfaizal Mohamed

2005-01-01

Gamma Spectrometry is widely used to determine the activity of gamma-ray emitter radionuclide inside a sample. Reporting the activity of the measurement for a sample should not be a single value only but it shall be associated with a reasonable uncertainty value since disintegration of radionuclide is a random/spontaneous process. This paper will focus on how the uncertainty was estimated, quantified and calculated, when measuring the activity of Cs-134 and Cs-137 in food and Ra-226, Ra-228 and K-40 in the environmental samples. (Author)

Ash contents of foodstuff samples in environmental radioactivity analysis

International Nuclear Information System (INIS)

Oikawa, Shinji; Ohta, Hiroshi; Hayano, Kazuhiko; Nonaka, Nobuhiro

2004-01-01

Statistical data of the ash content in various environmental samples obtained from an environmental radioactivity survey project commissioned by the Japanese government of Science and Technology Agency (at present Ministry of Education, Culture, Sports, Sciences and Technology) during the past 10 years are expressed for establishing a standard of ash content in environmental samples based on radioactivity analysis. The ash content for some kinds of environmental samples such as dietary food, milk, Japanese radish, spinach, fish, green tea and potato was reviewed in the light of statistical and stochastic viewpoints. For all of the samples reviewed in this paper, the coefficient of variation varied from 4.7% for milk to 36.3% for cabbage. Dietary food and milk samples were reviewed more than 1900 and 1400 samples, respectively. Especially, ash content of dietary food depended mainly on the dietary culture reflected on the period. However it showed an almost invariant distribution within 18.7% of coefficient of variation during the past 10 years. Pretreatment of environmental samples especially ashing processes are important from the viewpoint on environmental radioactivity analysis, which is one of the especial fields in analytical chemistry. Statistical reviewed data obtained in this paper may be useful for sample preparation. (author)

Determination of strontium-90 in the environmental samples at PINSTECH

International Nuclear Information System (INIS)

Perveen, N.; Aziz, A.

1979-01-01

Strontium-90 a bone seeking radionuclide and a long lived beta emitter is one of the toxic radionuclides detected in the environment arising mainly from the fall out from nuclear detonations. Its concentration in various environmental media such as air, precipitation, surface water, vegetables and other items of diet was measured. This report describes the method of collection, treatment and radiochemical analyses of environmental samples for the determination of Sr-90. The levels of Sr-90 concentration in these media are also recorded. (authors)

Three-phase double-arc plasma for spectrochemical analysis of environmental samples.

Science.gov (United States)

Mohamed, M M; Ghatass, Z F; Shalaby, E A; Kotb, M M; El-Raey, M

2000-12-01

A new instrument, which uses a three-phase current to support a double-arc argon plasma torch for evaporation, atomization and excitation of solid or powder samples, is described. The sampling arc is ignited between the first and second electrode while the excitation arc is ignited between the second and third electrode. Aerosol generated from the sample (first electrode) is swept by argon gas, through a hole in the second electrode (carbon tubing electrode), into the excitation plasma. A tangential stream of argon gas is introduced through an inlet orifice as a coolant gas for the second electrode. This gas stream forces the excitation arc discharge to rotate reproducibly around the electrode surface. Discharge rotation increases the stability of the excitation plasma. Spectroscopic measurements are made directly in the current-carrying region of the excitation arc. An evaluation of each parameter influencing the device performance was performed. Analytical calibration curves were obtained for Fe, Al, K, and Pb. Finally, the present technique was applied for the analysis of environmental samples. The present method appears to have significant, low cost analytical utility for environmental measurements.

Self-absorption corrections for gamma ray spectral measurements of 210Pb in environmental samples

International Nuclear Information System (INIS)

Miller, K.M.

1987-01-01

Theoretical considerations and experimental data are used to demonstrate the basic behaviour of the self-absorption effect of a sample matrix in gamma ray spectrometry, particularly as it relates to the analysis of 210 Pb in environmental media. The results indicate that it may not be appropriate to apply the commonly used self-absorption function in all cases. (orig.)

Quality assurance programme for environmental radioactivity measurements at the Hong Kong observatory

International Nuclear Information System (INIS)

Wong, M.C.; Mok, H.Y.

1999-01-01

The Hong Kong Observatory (HKO) runs an Environmental Radiation Monitoring Programme (ERMP) to monitor the environmental radiation levels in Hong Kong. In the ERMP, about 400 environmental samples are delivered to the HKO Radiation Laboratory each year for alpha, beta and gamma measurements. The quality of the radiation measurements is assured through an internal quality assurance programme and inter-laboratory comparison exercises

Influence of sample temperature and environmental humidity on measurements of benzene in ambient air by transportable GC-PID

Directory of Open Access Journals (Sweden)

C. Romero-Trigueros

2017-10-01

Full Text Available Calibration of in situ analysers of air pollutants is usually done with dry standards. In this paper, the influence of sample temperature and environmental humidity on benzene measurements by gas chromatography coupled with a photoionisation detector (GC-PID is studied. Two reference gas mixtures (40 and 5 µg m−3 nominal concentration benzene in air were subjected to two temperature cycles (20/5/20 °C and 20/35/20 °C and measured with two identical GC-PIDs. The change in sample temperature did not produce any significant change in readings. Regarding ambient humidity, the chromatographs were calibrated for benzene with dry gases and subjected to measure reference standards with humidity (20 and 80 % at 20 °C. When measuring a concentration of 0.5 µg m−3 benzene in air, the levels of humidity tested did not produce any significant interference in measurements taken with any of the analysers. However, when measuring a concentration of 40 µg m−3, biases in measurements of 18 and 21 % for each respective analyser were obtained when the relative humidity of the sample was 80 % at 20 °C. Further tests were carried out to study the nature of this interference. Results show that humidity interference depends on both the amount fractions of water vapour and benzene. If benzene concentrations in an area are close to its annual limit value (5 µg m−3, biases of 2.2 % can be expected when the absolute humidity is 8.6 g cm−3 – corresponding to a relative humidity of 50 % at 20 °C. This can be accounted for in the uncertainty budget of measurements with no need for corrections. If benzene concentrations are above the annual limit value, biases become higher. Thus, in these cases, actions should be taken to reduce the humidity interference, as an underestimation of benzene concentrations may cause a mismanagement of air quality in these situations.

Teaching environmental physics with a field measurement campaign

International Nuclear Information System (INIS)

Boman, Johan; Dynefors, Bertil; Kuehlmann-Berenzon, Sharon

2003-01-01

With 15 years of experience of teaching environmental physics, we still need to develop our curriculum. In this paper we present our findings from teaching environmental physics in close association with mathematical statistics in an applied field measurement campaign. Here not only environmental physics is taught, but also the concept of experimental planning, design, implementation, and evaluation of a field measurement campaign. The field measurement gives the students the opportunity to follow the whole process starting from experimental planning, including formulating the questions to answer, through design of the experiment, sample collection, analysis, and evaluation, together with the writing of a final report. All possible aspects of the problem that the students are working on can be carefully investigated, but the emphasis has been on understanding the whole process of carrying out a field campaign. This holistic view gives the students more interest in and better motivation for exploring the subject. This course gave the students insight into the field of interdisciplinary environmental research, promoted their creativity, and also gave the teachers a feeling of satisfaction

Osmium in environmental samples from Northeast Sweden

International Nuclear Information System (INIS)

Rodushkin, Ilia; Engstroem, Emma; Soerlin, Dieke; Ponter, Christer; Baxter, Douglas C.

2007-01-01

Osmium (Os) concentrations and 187 Os/ 188 Os isotope abundance ratios are presented for sedimentary materials, soils, humus, plants, mushrooms, mosses and lichens collected in the vicinity of the town of Lulea, Northeast Sweden, the data for biological specimens being the first reported. Contributions from sampling and varying exposure time to the observed environmental variability were evaluated. Sedimentary materials (from both fresh and brackish water) are most elevated in radiogenic 187 Os, followed by inorganic soil horizons, mushrooms and humus. The Os isotopic compositions of plants, mosses and lichens are much less radiogenic, with mean 187 Os/ 188 Os lying within a relatively narrow 0.3-0.6 range. Significant temporal variations in Os concentrations and isotopic compositions of plant samples are attributed to integrative uptake of airborne Os with non-radiogenic composition. Measured Os concentrations in biological matrices increase in the order: small shrub leaves (blueberry and lingonberry) ≤ spruce needles ≤ mushrooms ≤ tree leaves ≤ pine needles 4 ) in the environment. Though the Os content of samples from Northeast Sweden does not differ significantly from matrix-matched international reference materials (not certified for Os) of abiotic origin, the estimates of gaseous OsO 4 concentrations are roughly an order of magnitude higher than have been reported for particle-bound Os in other studies. The pronounced spatial variations between relatively closely situated sites in mean 187 Os/ 188 Os ratios for samples of the same species (presumably with the same dominating uptake mechanism) point to the presence of different local Os sources. This study therefore demonstrates that emissions of Os from automobile catalytic converters are not the only source of contemporary environmental contamination

Measurement of polybrominated diphenyl ethers in environmental matrix standard reference materials

Energy Technology Data Exchange (ETDEWEB)

Stapleton, H.; Schantz, M.; Wise, S. (National Institute of Standards and Technology)

2004-09-15

Polybrominated diphenyl ethers (PBDEs) are a class of emerging contaminants of concern as many studies have now demonstrated that these compounds are bioaccumulative, persistent and increasing in concentration in the environment. PBDEs are being detected in almost every environmental sample examined, and they have even been measured in samples collected in the Arctic, further demonstrating their persistence and potential for long range transport. More and more studies are continuing to examine the fate and transport of these flame retardant compounds in environmental samples and as such, reference materials are needed to provide quality control on these measurements. The National Institute of Standards and Technology (NIST) supports a national Standard Reference Material (SRM) program for measurement of organic contaminants such as PCBs, PAHs and chlorinated pesticides in environmental matrices. This current study was undertaken to provide reference measurements for PBDEs in selected SRMs that are currently used by various laboratories throughout the United States. These SRMs include matrices such as marine mammal blubber, lake trout tissue, mussel tissue, sediment, house dust and human serum. We report here reference values for 22 PBDE congeners that have been quantified in these seven types of SRMs.

The analysis study of plutonium in the environmental sample by mass spectrum combined with isotopic dilution

International Nuclear Information System (INIS)

Han Jun; Fu Zhonghua; Mao Xingen; Meng Fanben

2004-01-01

The technology of the rhenium filament carbonization was used to increase the ionization efficiency in this paper. The plutonium in the environmental sample was analyzed by Mass Spectrum combined with isotope dilution. Analysis of the 239 Pu blank in the process: The analysis of 239 Pu from the chemical process was carried out in order to establish the influence of the 239 Pu introduced from the process. The analysis results were shown in Table 1 sample 1 was not gone through the process, sample 2 and sample 3 were gone through the process. It was clear that there was no influence of the 239 Pu from the process within the deviation. Results and Discussions: The environmental samples which were dealed with the chemical method were prepared the sample of mass spectrum, The atomic ratio of the 239 Pu and 242 Pu in the environmental samples was measured by Mass Spectrum. The atomic ratio in the tracer 242 Pu was 0.01476±0.00007.The results for nuclide content in environment were given in Table 2. The content of 239 Pu in the tracer was high, so the existing of 239 Pu in the environmental samples can be determined by the changing of the atomic ratio of 242 Pu to 239 Pu. It was clear that there was 239 Pu in the environmental samples except the cypress leaves-2 and the pine leaves-3 within the deviation, and the content of 239 Pu were given in Table 2. Conclusion: a. Plutonium was separated and purified from the impurity by the anion-exchange and the electrodeposition, it was possible to provide the eligible mass spectrum sample. b. The measurement of plutonium in the environmental samples was not influenced by the flow of the background in the experiment. c. As the technology of the rhenium carbonization was used to increase the ionization efficiency, the content of plutonium which was about 10 -13 g in the environmental sample could be quantitatively analyzed by Mass Spectrum combined with isotope dilution. (authors)

Tentative reference method for measurement of tritium in environmental waters. Environmental monitoring series

International Nuclear Information System (INIS)

1975-12-01

A tentative reference method for the measurement of tritium in potable and nonpotable environmental water is described. Water samples are treated with sodium hydroxide and potassium permanganate and then a water fraction is separated from interferences by distillation. Two distillation procedures are described, a simple aqueous distillation for samples from potable water sources, and an aqueous-azeotropic-benzene distillation for nonpotable water sources. Alliquots of a designated distillate fraction are measured for tritium activity by liquid scintillation detection. Distillation recovery and counting efficiency factors are determined with tritium standards. Results are reported in picocuries per milliliter

Development of low-level environmental sampling capabilities for uranium at Brazilian and Argentine laboratories by ABACC

International Nuclear Information System (INIS)

Guidicini, Olga Mafra; Hembree Junior, Doyle M.; Carter, Joel A.; Hayes, Susan; Whitaker, Michael; Olsen, Khris

2003-01-01

The Brazilian-Argentine Agency for Accounting and Control of Nuclear Materials (ABACC) with assistance from the U.S. Department of Energy (DOE) began a program to evaluate environmental sampling capabilities at laboratories in Argentina and Brazil in June 1998. The program included staff training conducted in South America and the United States. Several laboratory evaluation exercises were also conducted using standard swipe samples prepared by the International Atomic Energy Agency (IAEA) and a National Institute of Standards and Technology Standard Reference Material 1547, Peach Leaves. The results of these exercises demonstrated that several laboratories were capable of accurately determining the total uranium and uranium isotopic distribution in the peach leaves. To build on these successes, another exercise using standard swipe samples prepared by the IAEA was conducted. A total of 8 sets of 15 swipe samples were prepared and distributed to the six ABACC support laboratories and to two of DOE's Network of Analytical Laboratories (NWAL) that support IAEA's environmental sampling program Throughout this project, the ABACC laboratories have shown steady progress in contamination control and improvements to the accuracy and precision of their measurements. The results of the latest exercises demonstrate that ABACC now has support laboratories in both Argentina and Brazil that have the capability to measure both the amount and isotopic composition of uranium at levels expected in typical environmental samples (i.e., sub-microgram quantities). This presentation will discuss the final results for the exercise with uranium swipe samples and discuss future activities to develop measurement capabilities for total and isotopic plutonium in environmental samples. (author)

New trends in sample preparation techniques for environmental analysis.

Science.gov (United States)

Ribeiro, Cláudia; Ribeiro, Ana Rita; Maia, Alexandra S; Gonçalves, Virgínia M F; Tiritan, Maria Elizabeth

2014-01-01

Environmental samples include a wide variety of complex matrices, with low concentrations of analytes and presence of several interferences. Sample preparation is a critical step and the main source of uncertainties in the analysis of environmental samples, and it is usually laborious, high cost, time consuming, and polluting. In this context, there is increasing interest in developing faster, cost-effective, and environmentally friendly sample preparation techniques. Recently, new methods have been developed and optimized in order to miniaturize extraction steps, to reduce solvent consumption or become solventless, and to automate systems. This review attempts to present an overview of the fundamentals, procedure, and application of the most recently developed sample preparation techniques for the extraction, cleanup, and concentration of organic pollutants from environmental samples. These techniques include: solid phase microextraction, on-line solid phase extraction, microextraction by packed sorbent, dispersive liquid-liquid microextraction, and QuEChERS (Quick, Easy, Cheap, Effective, Rugged and Safe).

Evaluation of Brazilian intercomparison program data from 1991 to 1995 of radionuclide assays in environmental samples

International Nuclear Information System (INIS)

Vianna, Maria Elizabeth Couto M.; Tauhata, Luiz; Oliveira, Antonio Eduardo de; Oliveira, Josue Peter de; Clain, Almir Faria; Ferreira, Ana Cristina M.

1998-01-01

Historical radioanalytical data from the Institute of Radiation Protection and Dosimetry (IRD) national intercomparison program from 1991 to 1995 were analyzed to evaluate the performance of sixteen Brazilian laboratories in radionuclide analyses in environmental samples. Data are comprised of measurements of radionuclides in 435 spiked environmental samples distributed in fifteen intercomparison runs comprised of 955 analyses. The general and specific radionuclide performances of the participating laboratories were evaluated relative to the reference value. Data analysis encourages improvements in beta emitter measurements

Efficiency corrections in determining the (137)Cs inventory of environmental soil samples by using relative measurement method and GEANT4 simulations.

Science.gov (United States)

Li, Gang; Liang, Yongfei; Xu, Jiayun; Bai, Lixin

2015-08-01

The determination of (137)Cs inventory is widely used to estimate the soil erosion or deposition rate. The generally used method to determine the activity of volumetric samples is the relative measurement method, which employs a calibration standard sample with accurately known activity. This method has great advantages in accuracy and operation only when there is a small difference in elemental composition, sample density and geometry between measuring samples and the calibration standard. Otherwise it needs additional efficiency corrections in the calculating process. The Monte Carlo simulations can handle these correction problems easily with lower financial cost and higher accuracy. This work presents a detailed description to the simulation and calibration procedure for a conventionally used commercial P-type coaxial HPGe detector with cylindrical sample geometry. The effects of sample elemental composition, density and geometry were discussed in detail and calculated in terms of efficiency correction factors. The effect of sample placement was also analyzed, the results indicate that the radioactive nuclides and sample density are not absolutely uniform distributed along the axial direction. At last, a unified binary quadratic functional relationship of efficiency correction factors as a function of sample density and height was obtained by the least square fitting method. This function covers the sample density and height range of 0.8-1.8 g/cm(3) and 3.0-7.25 cm, respectively. The efficiency correction factors calculated by the fitted function are in good agreement with those obtained by the GEANT4 simulations with the determination coefficient value greater than 0.9999. The results obtained in this paper make the above-mentioned relative measurements more accurate and efficient in the routine radioactive analysis of environmental cylindrical soil samples. Copyright © 2015 Elsevier Ltd. All rights reserved.

Technical Note: New methodology for measuring viscosities in small volumes characteristic of environmental chamber particle samples

Directory of Open Access Journals (Sweden)

L. Renbaum-Wolff

2013-01-01

Full Text Available Herein, a method for the determination of viscosities of small sample volumes is introduced, with important implications for the viscosity determination of particle samples from environmental chambers (used to simulate atmospheric conditions. The amount of sample needed is < 1 μl, and the technique is capable of determining viscosities (η ranging between 10⁻³ and 10³ Pascal seconds (Pa s in samples that cover a range of chemical properties and with real-time relative humidity and temperature control; hence, the technique should be well-suited for determining the viscosities, under atmospherically relevant conditions, of particles collected from environmental chambers. In this technique, supermicron particles are first deposited on an inert hydrophobic substrate. Then, insoluble beads (~1 μm in diameter are embedded in the particles. Next, a flow of gas is introduced over the particles, which generates a shear stress on the particle surfaces. The sample responds to this shear stress by generating internal circulations, which are quantified with an optical microscope by monitoring the movement of the beads. The rate of internal circulation is shown to be a function of particle viscosity but independent of the particle material for a wide range of organic and organic-water samples. A calibration curve is constructed from the experimental data that relates the rate of internal circulation to particle viscosity, and this calibration curve is successfully used to predict viscosities in multicomponent organic mixtures.

Radiochemical separation of actinides for their determination in environmental samples and waste products

Energy Technology Data Exchange (ETDEWEB)

Gleisberg, B [Nuclear Engineering and Analytics Rossendorf, Inc. (VKTA), Dresden (Germany)

1997-03-01

The determination of low level activities of actinides in environmental samples and waste products makes high demands on radiochemical separation methods. Artificial and natural actinides were analyzed in samples form the surrounding areas of NPP and of uranium mines, incorporation samples, solutions containing radioactive fuel, solutions and solids resutling from the process, and in wastes. The activities are measured by {alpha}-spectrometry and {gamma}-spectrometry. (DG)

Determination of /sup 240/Pu//sup 239/Pu ratio in the environmental samples based on the measurement of Lx/. cap alpha. -ray activity ratio

Energy Technology Data Exchange (ETDEWEB)

Komura, K.; Sakanoue, M.; Yamamoto, M.

1984-06-01

The determination of the /sup 240/Pu//sup 239/Pu isotopic ratio in environmental samples has been attempted by the measurement of the Lx/..cap alpha..-ray activity ratio using a Ge-LEPS (low-energy photon spectrometer) and a surface-barrier Si detector. By this method, interesting data were obtained for various samples collected from Thule, Greenland, Bikini Atoll and Nagasaki, as well as for some soils collected from near and off-site locations of atomic power stations.

Osmium in environmental samples from Northeast Sweden

Energy Technology Data Exchange (ETDEWEB)

Rodushkin, Ilia [Division of Applied Geology, Lulea University of Technology, S-971 87 Lulea (Sweden); ALS Laboratory Group, ALS Analytica AB, Aurorum 10, S-977 75 Lulea (Sweden)], E-mail: ilia.rodushkin@alsglobal.com; Engstroem, Emma [Division of Applied Geology, Lulea University of Technology, S-971 87 Lulea (Sweden); Soerlin, Dieke; Ponter, Christer; Baxter, Douglas C. [ALS Laboratory Group, ALS Analytica AB, Aurorum 10, S-977 75 Lulea (Sweden)

2007-11-01

Osmium (Os) concentrations and {sup 187}Os/{sup 188}Os isotope abundance ratios are presented for sedimentary materials, soils, humus, plants, mushrooms, mosses and lichens collected in the vicinity of the town of Lulea, Northeast Sweden, the data for biological specimens being the first reported. Contributions from sampling and varying exposure time to the observed environmental variability were evaluated. Sedimentary materials (from both fresh and brackish water) are most elevated in radiogenic {sup 187}Os, followed by inorganic soil horizons, mushrooms and humus. The Os isotopic compositions of plants, mosses and lichens are much less radiogenic, with mean {sup 187}Os/{sup 188}Os lying within a relatively narrow 0.3-0.6 range. Significant temporal variations in Os concentrations and isotopic compositions of plant samples are attributed to integrative uptake of airborne Os with non-radiogenic composition. Measured Os concentrations in biological matrices increase in the order: small shrub leaves (blueberry and lingonberry) {<=} spruce needles {<=} mushrooms {<=} tree leaves {<=} pine needles < mosses << lichens. The concentrations found in three different species of plant were used to provide the first estimates of gaseous osmium tetroxide (OsO{sub 4}) in the environment. Though the Os content of samples from Northeast Sweden does not differ significantly from matrix-matched international reference materials (not certified for Os) of abiotic origin, the estimates of gaseous OsO{sub 4} concentrations are roughly an order of magnitude higher than have been reported for particle-bound Os in other studies. The pronounced spatial variations between relatively closely situated sites in mean {sup 187}Os/{sup 188}Os ratios for samples of the same species (presumably with the same dominating uptake mechanism) point to the presence of different local Os sources. This study therefore demonstrates that emissions of Os from automobile catalytic converters are not the only

Gamma spectrometric analyses of environmental samples at PINSTECH

International Nuclear Information System (INIS)

Faruq, M.U.; Parveen, N.; Ahmed, B.; Aziz, A.

1979-01-01

Gamma spectrometric analyses of air and other environmental samples from PINSTECH were carried out. Air particulate samples were analyzed by a Ge(Li) detector on a computer-based multichannel analyzer. Other environmental samples were analyzed by a Na(T1) scintillation detector spectrometer and a multichannel analyzer with manual analysis. Concentration of radionuclides in the media was determined and the sources of their production were identified. Age of the fall out was estimated from the ratios of the fission products. (authors)

Radionuclide determination in environmental samples by inductively coupled plasma mass spectrometry

International Nuclear Information System (INIS)

Lariviere, Dominic; Taylor, Vivien F.; Evans, R. Douglas; Cornett, R. Jack

2006-01-01

The determination of naturally occurring and anthropogenic radionuclides in the environment by inductively coupled plasma mass spectrometry has gained recognition over the last fifteen years, relative to radiometric techniques, as the result of improvement in instrumental performance, sample introduction equipment, and sample preparation. With the increase in instrumental sensitivity, it is now possible to measure ultratrace levels (fg range) of many radioisotopes, including those with half-lives between 1 and 1000 years, without requiring very complex sample pre-concentration schemes. However, the identification and quantification of radioisotopes in environmental matrices is still hampered by a variety of analytical issues such as spectral (both atomic and molecular ions) and non-spectral (matrix effect) interferences and instrumental limitations (e.g., abundance sensitivity). The scope of this review is to highlight recent analytical progress and issues associated with the determination of radionuclides by inductively coupled plasma mass spectrometry. The impact of interferences, instrumental limitations (e.g., degree of ionization, abundance sensitivity, detection limits) and low sample-to-plasma transfer efficiency on the measurement of radionuclides by inductively coupled plasma mass spectrometry will be described. Solutions that overcome these issues will be discussed, highlighting their pros and cons and assessing their impact on the measurement of environmental radioactivity. Among the solutions proposed, mass and chemical resolution through the use of sector-field instruments and chemical reactions/collisions in a pressurized cell, respectively, will be described. Other methods, such as unique sample introduction equipment (e.g., laser ablation, electrothermal vaporisation, high efficiency nebulization) and instrumental modifications/optimizations (e.g., instrumental vacuum, radiofrequency power, guard electrode) that improve sensitivity and performance

Sampling quality assurance guidance in support of EM environmental sampling and analysis activities

International Nuclear Information System (INIS)

1994-05-01

This document introduces quality assurance guidance pertaining to the design and implementation of sampling procedures and processes for collecting environmental data for DOE's Office of EM (Environmental Restoration and Waste Management)

TECHNIQUES WITH POTENTIAL FOR HANDLING ENVIRONMENTAL SAMPLES IN CAPILLARY ELECTROPHORESIS

Science.gov (United States)

An assessment of the methods for handling environmental samples prior to capillary electrophoresis (CE) is presented for both aqueous and solid matrices. Sample handling in environmental analyses is the subject of ongoing research at the Environmental Protection Agency's National...

Conformity Assessment in Nuclear Material and Environmental Sample Analysis

International Nuclear Information System (INIS)

Aregbe, Y.; Jakopic, R.; Richter, S.; Venchiarutti, C.

2015-01-01

Safeguards conclusions are based to a large extent on comparison of measurement results between operator and safeguards laboratories. Measurement results must state traceability and uncertainties to be comparable. Recent workshops held at the IAEA and in the frame of the European Safeguards Research and Development Association (ESARDA), reviewed different approaches for Nuclear Material Balance Evaluation (MBE). Among those, the ''bottom-up'' approach requires assessment of operators and safeguards laboratories measurement systems and capabilities. Therefore, inter-laboratory comparisons (ILCs) with independent reference values provided for decades by JRC-IRMM, CEA/CETAMA and US DOE are instrumental to shed light on the current state of practice in measurements of nuclear material and environmental swipe samples. Participating laboratories are requested to report the measurement results with associated uncertainties, and have the possibility to benchmark those results against independent and traceable reference values. The measurement capability of both the IAEA Network of Analytical Laboratories (NWAL) and the nuclear operator's analytical services participating in ILCs can be assessed against the independent reference values as well as against internationally agreed quality goals, in compliance with ISO 13528:2005. The quality goals for nuclear material analysis are the relative combined standard uncertainties listed in the ITV2010. Concerning environmental swipe sample analysis, the IAEA defined measurement quality goals applied in conformity assessment. The paper reports examples from relevant inter-laboratory comparisons, looking at laboratory performance according to the purpose of the measurement and the possible use of the result in line with the IUPAC International Harmonized Protocol. Tendencies of laboratories to either overestimate and/or underestimate uncertainties are discussed using straightforward graphical tools to evaluate

Hanford Site Environmental Surveillance Master Sampling Schedule for Calendar Year 2008

Energy Technology Data Exchange (ETDEWEB)

Bisping, Lynn E.

2008-01-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by Pacific Northwest National Laboratory for the U.S. Department of Energy. Sampling is conducted to evaluate levels of radioactive and nonradioactive pollutants in the Hanford environs, as required in DOE Order 450.1, "Environmental Protection Program," and DOE Order 5400.5, "Radiation Protection of the Public and the Environment." The environmental surveillance sampling design is described in the "Hanford Site Environmental Monitoring Plan, United States Department of Energy, Richland Operations Office." This document contains the calendar year 2008 schedule for the routine collection of samples for the Surface Environmental Surveillance Project and Drinking Water Monitoring Project. Each section includes sampling locations, sampling frequencies, sample types, and analyses to be performed. In some cases, samples are scheduled on a rotating basis. If a sample will not be collected in 2008, the anticipated year for collection is provided. Maps showing approximate sampling locations are included for media scheduled for collection in 2008.

Determination of Sr-90 in environmental samples using solid phase extraction disk

International Nuclear Information System (INIS)

Zal U'yun Wan Mahmood

2002-01-01

A method is described for determination of Sr-90 in environmental samples using solid phase extraction disk (Empore TM Strontium Rad Disk) and GM counter. To determine the optimum condition for capacity of Empore TM Strontium Rad Disk, its characterization studies such as the effects Sr content, acidity (molarity) of acids, presence of Ca 2+ and other major ions (Na + , Mg 2+ etc), influence of interference (Pb and Bi) and others were carried out. An optimized the using of Empore TM Strontium Rad Disk for determination of Sr-90 was validated by application to environmental samples. Quantitative recoveries above 95%for Sr (stable) were recorded in 6M HCl condition. Typical environmental samples may contain an assortment of anionic and cationic species, but in general, Empore TM Strontium Rad Disk has enough capacity to effectively separate Sr for wide variety of aqueous solutions. Sr recovery in a matrix-free or the content of matrix less than 300 mg/sample is typically greater than 99% is reported in this research work. In particular, sample, which may contain interference such as Pb and Bi would require an addition separation step before processing to ensure an accurate measurement of Sr. In this research work, radiotracer 85 Sr was used to monitor the behavior of Sr and calculation its recovery. For analytical methods that can count Y-90, the Sr-90 activity/concentration in environmental sample was calculated. The concentration of Sr-90 in ash sample (Quality Controled Sample) of 276 ± 18 Bq/kg ash was determined from Y-90 activity. The relative percent difference of 1.1% was achievable for Empore TM Sr-Rad Disk methods when compared to the conventional method (fumed-HNO 3 method) - 279 ± 11 Bq/kg ash. (Author)

Efficiency of tritium measurement in the environmental water by electrolysis enrichment

Energy Technology Data Exchange (ETDEWEB)

Koganezawa, T.; Iida, T. [Nagoya Univ., Graduate School of Engineering, Nagoya, Aichi (Japan); Sakuma, Y.; Yamanishi, H. [National Inst. for Fusion Science, Toki, Gifu (Japan); Ogata, Y. [Nagoya Univ., School of Health Sciences, Nagoya, Aichi (Japan); Tsuji, N. [Japan Air-conditioning Service Co. and Ltd., Nagoya, Aichi (Japan); Kakiuchi, M. [Gakushuin Univ., Faculty of Science, Tokyo (Japan); Satake, H. [Toyama Univ., Faculty of Science, Toyama (Japan)

2002-06-01

Now tritium concentration in the environmental water is 0.5-2 Bq{center_dot}L{sup -1} in Japan. Tritium concentration cannot be measured accurately by liquid scintillation method, because the minimum detectable limits of liquid scintillation method is 0.5 Bq{center_dot}L{sup -1}. Therefore, one needs to enrich tritium concentration in the environmental water. Although the most popular method for tritium enrichment is electrolysis, the electrolysis takes much time and labor for distilling sample water at before and after the electrolysis. The purpose of this study is to investigate the possibility of more convenient method for tritium measurement. The method substitutes filtration for distillation at before electrolysis and omits distillation at after electrolysis. The method enables by using the electrolysis with solid polymer electrode. We performed two kinds of experiment to confirm the possibility of the method. First, impurities eluted from electrolysis installation with ultra pure water as sample was measured. Some impurities were eluted into the sample, but they brought noneffective quenching. Secondly, we applied new method to the environmental waters. Substituting for distillation, two filtration, 0.1 {mu}m filtration and reverse osmosis method, were investigated. Impurities in the samples by the filtrations were somewhat higher than that by the distillation, they brought noneffective quenching. We, however, observed distemper of the electrolysis happened by electrolysing filtered sample. Distillation is substituted filtration at before enrichment and omitted at after enrichment, leaving the influence of quenching out of consideration. (author)

Efficiency of tritium measurement in the environmental water by electrolysis enrichment

International Nuclear Information System (INIS)

Koganezawa, T.; Iida, T.; Sakuma, Y.; Yamanishi, H.; Ogata, Y.; Tsuji, N.; Kakiuchi, M.; Satake, H.

2002-01-01

Now tritium concentration in the environmental water is 0.5-2 Bq·L -1 in Japan. Tritium concentration cannot be measured accurately by liquid scintillation method, because the minimum detectable limits of liquid scintillation method is 0.5 Bq·L -1 . Therefore, one needs to enrich tritium concentration in the environmental water. Although the most popular method for tritium enrichment is electrolysis, the electrolysis takes much time and labor for distilling sample water at before and after the electrolysis. The purpose of this study is to investigate the possibility of more convenient method for tritium measurement. The method substitutes filtration for distillation at before electrolysis and omits distillation at after electrolysis. The method enables by using the electrolysis with solid polymer electrode. We performed two kinds of experiment to confirm the possibility of the method. First, impurities eluted from electrolysis installation with ultra pure water as sample was measured. Some impurities were eluted into the sample, but they brought noneffective quenching. Secondly, we applied new method to the environmental waters. Substituting for distillation, two filtration, 0.1 μm filtration and reverse osmosis method, were investigated. Impurities in the samples by the filtrations were somewhat higher than that by the distillation, they brought noneffective quenching. We, however, observed distemper of the electrolysis happened by electrolysing filtered sample. Distillation is substituted filtration at before enrichment and omitted at after enrichment, leaving the influence of quenching out of consideration. (author)

Reproducibility of measurement of the environmental carbon-14 samples prepared by the gel suspension method

International Nuclear Information System (INIS)

Ohura, Hirotaka; Wakabayashi, Genichiro; Nakamura, Kouji; Okai, Tomio; Matoba, Masaru; Kakiuchi, Hideki; Momoshima, Noriyuki; Kawamura, Hidehisa.

1997-01-01

Simple liquid scintillation counting technique for the assay of 14 C in the environment was developed. This technique was done by using gel suspension method, in which sample preparation is very simple and requires no special equipments. The reproducibility of this technique was considered and it was shown that the gel suspension method had enough reproducibility to monitor the environmental 14 C. (author)

National comparison on volume sample activity measurement methods

International Nuclear Information System (INIS)

Sahagia, M.; Grigorescu, E.L.; Popescu, C.; Razdolescu, C.

1992-01-01

A national comparison on volume sample activity measurements methods may be regarded as a step toward accomplishing the traceability of the environmental and food chain activity measurements to national standards. For this purpose, the Radionuclide Metrology Laboratory has distributed 137 Cs and 134 Cs water-equivalent solid standard sources to 24 laboratories having responsibilities in this matter. Every laboratory has to measure the activity of the received source(s) by using its own standards, equipment and methods and report the obtained results to the organizer. The 'measured activities' will be compared with the 'true activities'. A final report will be issued, which plans to evaluate the national level of precision of such measurements and give some suggestions for improvement. (Author)

Diagnostic herd sensitivity using environmental samples

DEFF Research Database (Denmark)

Vigre, Håkan; Josefsen, Mathilde Hartmann; Seyfarth, Anne Mette

either at farm or slaughter. Three sample matrices were collected; dust samples (5 environmental swabs), nasal swabs (10 pools with 5 animals per pool) and air samples (1 filter). Based on the assumption that MRSA occurred in all 48 herds the overall herd sensitivity was 58% for nasal swabs, 33% for dust....... In our example, the prevalence of infected pigs in each herd was estimated from the pooled samples of nasal swabs. Logistic regression was used to estimate the effect of animal prevalence on the probability to detect MRSA in the dust and air samples at herd level. The results show a significant increase...

Determination of short-lived trace elements in environmental samples by neutron activation analysis

International Nuclear Information System (INIS)

Wardani, S.; Sihombing, E.; Hamzah, A.; Rochidi; Hery, P.S.; Hartaman, S.; Iman, J.

1998-01-01

Concentration of a short-lived trace elements in environmental samples were determined by neutron activation analysis, a counting loss often occur due to the high counting rate. A Pile-Up Rejecter (PUR) electric circuit was installed in counting a short-lived trace elements by a γ-ray spectrometer in order to correct a counting loss. The samples were irradiated for 30∼60 seconds at neutron flux of 3.5 x 10 12 n.cm -2 .s -1 , then the samples cooled for 120 second and counted for 180 second using this system. The nuclides concentration in the varieties environmental samples have a difference analysis result, was more accurate and precise, which the measured result would be 30 % more higher by PUR system than the result would be counted using a conventional γ-ray spectrometry method

Middlesex Sampling Plant environmental report for calendar year 1989, Middlesex, New Jersey

International Nuclear Information System (INIS)

1990-05-01

The environmental monitoring program, which began in 1980, was continued in 1989 at the former Middlesex Sampling Plant (MSP) site, located in the Borough of Middlesex, New Jersey. The MSP site is part of the Formerly Utilized Sites Remedial Action Program (FUSRAP), a Department of Energy (DOE) program to decontaminate or otherwise control sites where residual radioactive materials remain either from the early years of the nation's atomic energy program or from commercial operations causing conditions that Congress has authorized DOE to remedy. The monitoring program at MSP measures radon concentrations in air; external gamma radiation levels; and uranium and radium concentrations in surface water, groundwater, and sediment. Additionally, several nonradiological parameters are measured in groundwater samples. To verify that the site is in compliance with the DOE radiation protection standard (100 mrem/yr) and to assess its potential effect on public health, the radiation dose was calculated for a hypothetical maximally exposed individual. This report presents the findings of the environmental monitoring program conducted in the area of the Middlesex Sampling Plant (MSP) site during calendar year 1989. 17 refs., 16 figs., 16 tabs

Middlesex Sampling Plant environmental report for calendar year 1989, Middlesex, New Jersey

Energy Technology Data Exchange (ETDEWEB)

1990-05-01

The environmental monitoring program, which began in 1980, was continued in 1989 at the former Middlesex Sampling Plant (MSP) site, located in the Borough of Middlesex, New Jersey. The MSP site is part of the Formerly Utilized Sites Remedial Action Program (FUSRAP), a Department of Energy (DOE) program to decontaminate or otherwise control sites where residual radioactive materials remain either from the early years of the nation's atomic energy program or from commercial operations causing conditions that Congress has authorized DOE to remedy. The monitoring program at MSP measures radon concentrations in air; external gamma radiation levels; and uranium and radium concentrations in surface water, groundwater, and sediment. Additionally, several nonradiological parameters are measured in groundwater samples. To verify that the site is in compliance with the DOE radiation protection standard (100 mrem/yr) and to assess its potential effect on public health, the radiation dose was calculated for a hypothetical maximally exposed individual. This report presents the findings of the environmental monitoring program conducted in the area of the Middlesex Sampling Plant (MSP) site during calendar year 1989. 17 refs., 16 figs., 16 tabs.

Detection of the actinides and cesium from environmental samples

Science.gov (United States)

Snow, Mathew Spencer

Detection of the actinides and cesium in the environment is important for a variety of applications ranging from environmental remediation to safeguards and nuclear forensics. The utilization of multiple different elemental concentrations and isotopic ratios together can significantly improve the ability to attribute contamination to a unique source term and/or generation process; however, the utilization of multiple elemental "signatures" together from environmental samples requires knowledge of the impact of chemical fractionation for various elements under a variety of environmental conditions (including predominantly aqueous versus arid conditions). The research reported in this dissertation focuses on three major areas: 1. Improving the understanding of actinide-mineral interactions at ultra-low concentrations. Chapter 2 reports a batch sorption and modeling study of Np(V) sorption to the mineral goethite from attomolar to micromolar concentrations. 2. Improving the detection capabilities for Thermal Ionization Mass Spectrometry (TIMS) analyses of ultra-trace cesium from environmental samples. Chapter 4 reports a new method which significantly improves the chemical yields, purification, sample processing time, and ultimately, the detection limits for TIMS analyses of femtogram quantities of cesium from a variety of environmental sample matrices. 3. Demonstrating how actinide and cesium concentrations and isotopic ratios from environmental samples can be utilized together to determine a wealth of information including environmental transport mechanisms (e.g. aqueous versus arid transport) and information on the processes which generated the original material. Chapters1, 3 and 5 demonstrate these principles using Pu, Am, Np, and Cs concentrations and isotopic ratios from contaminated soils taken near the Subsurface Disposal Area (SDA) of Idaho National Laboratory (INL) (a low level radioactive waste disposal site in southeastern Idaho).

169 Résumé Abstract Measure of uranium in some samples of ...

African Journals Online (AJOL)

youness

puits et par activation neutronique. Mots-clés : Uranium, Radioactivité naturelle, Coraux, Coquilles de mollusques, lichens, travertins, Carbonates. Abstract. Measure of uranium in some samples of natural deposits in Morocco: environmental implications. In this work, we report the measurement results of uranium content in.

Contributions for the application of a phoswich detector on the analysis of environmental samples

International Nuclear Information System (INIS)

Dalaqua Junior, L.

1989-01-01

The characteristics of a phoswich detector and the parameters of the pulse shape descrimination system are evaluated aiming the application on environmental analysis by direct low level gamma ray spectrometry. The calibration curves and adjustments for the pulse discrimination, detector resolution and homogeneity measurements are presented. Background reduction and the 210 Pb detection eficiency on evaporated sources are evaluated. The results obtained demonstrates the application potentiality on the analysis of environmental samples due to a high detection eficiency and good geometry conditions to the measurements. (author) [pt

Cesium-137 and natural radionuclides in soils from southern Brazil and soils and others environmental samples from Antarctic

International Nuclear Information System (INIS)

Schuch, L.A.

1993-04-01

This work presents a study of environmental artificial and natural radioactivity levels in soil samples from the Southern Brazil and in soils and other environmental samples form Antarctica. Artificial radioactivity was determined by measuring Cs-137 which is a 30.1 year half-life man-made radionuclide produced in the past by atmospheric tests of nuclear weapons. Natural radioactivity was determined by measuring some radionuclides belonging to Th-232 and U-238 natural radioactive families, and of K-40 concentrations. Several types of soils from Southern Brazil; and soil samples, marine sediments, lichens, mosses and algae collected at King George and other nearby islands (South Shetland Archipelago, Antarctica) were analyzed. A gamma-ray spectrometer was used to measure radioactivity levels of the collected samples and its overall characteristics are analyzed in this work. (author)

Environmental sample accounting at the Savannah River Plant

International Nuclear Information System (INIS)

Zeigler, C.C.; Wood, M.B.

1978-01-01

At the Savannah River Plant Environmental Monitoring Laboratories, a computer-based systematic accounting method was developed to ensure that all scheduled samples are collected, processed through the laboratory, and counted without delay. The system employs an IBM 360/195 computer with a magnetic tape master file, an online disk file, and cathode ray tube (CRT) terminals. Scheduling and accounting are accomplished using computer-generated schedules, bottle labels, and output/ input cards. A printed card is issued for the collecting, analyzing, and counting of each scheduled sample. The card also contains information for the personnel who are to perform the work, e.g., sample location, aliquot to be processed, and procedure to be used. Manual entries are made on the card when each step in the process is completed. Additional pertinent data such as the reason a sample is not collected, the need for a nonstandard aliquot, and field measurement results are keypunched and then read into the computer files as required. The computer files are audited daily and summaries showing samples not processed in pre-established normal schedules are provided. The progress of sample analyses is readily determined at any time using the CRT terminal. Historic data are maintained on magnetic tape, and workload summaries showing the number of samples and number of determinations per month are issued. (author)

Development of a simplified method for Tritium measurement in the environmental water

International Nuclear Information System (INIS)

Sakuma, Y.; Yamanishi, H.; Iida, T.; Koganezawa, T.; Kakiuchi, M.; Satake, H.

2002-01-01

In Japan the tritium concentrations in the environmental water figure out at approximately 0.5-2Bq/kg-H 2 O and tends to get a little lower than at the moment. The least detectable limit enabled to count by the liquid scintillation counter attained to merely 0.4Bq/kg-H 2 O. It can survey that it is likely to have been impossible to immediately measure a tritium concentration in an environmental water by the liquid scintillation method. Although there can be some alternative methods, the liquid scintillation together with electrolysis enrichment must be the most effective measurement because we do not need to change any useful managements. We already reported that an immediate counting by the liquid scintillation method for the measurement of environmental samples such as rain, river and tap waters, the membrane filtration was an available alternative way to the distillation of the low level water samples

Environmental Measurements Laboratory. Environmental report, September 1, 1980-March 1, 1981

International Nuclear Information System (INIS)

Hardy, E.P. Jr.

1981-01-01

This report presents current information from the EML environmental programs, the Air Monitoring Section of the Bhabha Atomic Research Centre in India, the NASA Lewis Research Center and the Radiological and Environmental Research Division at Argonne National Laboratory. The initial section consists of interpretive reports and notes dealing with global movement of radioactive debris from nuclear tests, vertical distribution of short-lived radionuclides in the lower stratosphere at the end of 1980, stratospheric radionuclide and trace gas inventories, plutonium isotopes in stratospheric filtered air, sulfur dioxide measurements in New York City, estimates of lead, manganese, aluminum and iron in atmospheric deposition at American Samoa, chemical composition of deposition at seven US locations, intercomparison of trace element analyses of commercially available reference materials, evaluation of analytical methods for polycyclic aromatic hydrocarbons in sediment, and quality control assessments of radionuclide analyses of surface air filters, biological and deposition samples and of chemical analyses of precipitation. Subsequent sections include tabulations of Sr-90 fallout, chemical constituents of wet and dry deposition, radionuclides and trace metals in surface air, radioactivity and trace gases sampled in the stratosphere by aircraft and balloons, Sr-90 in San Francisco and New York diet, milk and tap water, and Cs-137 in Chicago foods. A bibliography of recent publications related to environmental studies is also presented

Assessment of PDMS-water partition coefficients: implications for passive environmental sampling of hydrophobic organic compounds

Science.gov (United States)

DiFilippo, Erica L.; Eganhouse, Robert P.

2010-01-01

Solid-phase microextraction (SPME) has shown potential as an in situ passive-sampling technique in aquatic environments. The reliability of this method depends upon accurate determination of the partition coefficient between the fiber coating and water (Kf). For some hydrophobic organic compounds (HOCs), Kf values spanning 4 orders of magnitude have been reported for polydimethylsiloxane (PDMS) and water. However, 24% of the published data examined in this review did not pass the criterion for negligible depletion, resulting in questionable Kf values. The range in reported Kf is reduced to just over 2 orders of magnitude for some polychlorinated biphenyls (PCBs) when these questionable values are removed. Other factors that could account for the range in reported Kf, such as fiber-coating thickness and fiber manufacturer, were evaluated and found to be insignificant. In addition to accurate measurement of Kf, an understanding of the impact of environmental variables, such as temperature and ionic strength, on partitioning is essential for application of laboratory-measured Kf values to field samples. To date, few studies have measured Kf for HOCs at conditions other than at 20 degrees or 25 degrees C in distilled water. The available data indicate measurable variations in Kf at different temperatures and different ionic strengths. Therefore, if the appropriate environmental variables are not taken into account, significant error will be introduced into calculated aqueous concentrations using this passive sampling technique. A multiparameter linear solvation energy relationship (LSER) was developed to estimate log Kf in distilled water at 25 degrees C based on published physicochemical parameters. This method provided a good correlation (R2 = 0.94) between measured and predicted log Kf values for several compound classes. Thus, an LSER approach may offer a reliable means of predicting log Kf for HOCs whose experimental log Kf values are presently unavailable. Future

Development of analytical techniques for safeguards environmental samples at JAEA

International Nuclear Information System (INIS)

Sakurai, Satoshi; Magara, Masaaki; Usuda, Shigekazu; Watanabe, Kazuo; Esaka, Fumitaka; Hirayama, Fumio; Lee, Chi-Gyu; Yasuda, Kenichiro; Inagawa, Jun; Suzuki, Daisuke; Iguchi, Kazunari; Kokubu, Yoko S.; Miyamoto, Yutaka; Ohzu, Akira

2007-01-01

JAEA has been developing, under the auspices of the Ministry of Education, Culture, Sports, Science and Technology of Japan, analytical techniques for ultra-trace amounts of nuclear materials in environmental samples in order to contribute to the strengthened safeguards system. Development of essential techniques for bulk and particle analysis, as well as screening, of the environmental swipe samples has been established as ultra-trace analytical methods of uranium and plutonium. In January 2003, JAEA was qualified, including its quality control system, as a member of the JAEA network analytical laboratories for environmental samples. Since 2004, JAEA has conducted the analysis of domestic and the IAEA samples, through which JAEA's analytical capability has been verified and improved. In parallel, advanced techniques have been developed in order to expand the applicability to the samples of various elemental composition and impurities and to improve analytical accuracy and efficiency. This paper summarizes the trace of the technical development in environmental sample analysis at JAEA, and refers to recent trends of research and development in this field. (author)

Environmental methodology. Sampling and preparing fresh water organisms. Measuring of emitting radionuclides

International Nuclear Information System (INIS)

Foulquier, Luc; Philippot, J.C.; Baudin-Jaulent, Yvette.

1982-05-01

This paper provides some initial responses to questions asked by users of radioecological documents. By using aquatic plants and fish drawn ''in situ'' the authors' results often reveal very low activity levels; they make a point of knowing how to deal with such levels, since the fundamental objective is to interpret transfer mechanisms. The establishment of the environmental level of radioactivity requires that the write-ups produced demonstrate the use of reproducible methods, and contain results for which the extent of reliability is clearly specified. Aquatic plants and fish are, among all fresh water organisms, the most interesting links in the study of artificial and natural radioactivity. By systematically using concrete examples, this work reaffirms the precautions that should be taken in a site study. Once the objective is clearly defined, the properties to give to the sampling can be specified [fr

Improved sample preparation and counting techniques for enhanced tritium measurement sensitivity

Science.gov (United States)

Moran, J.; Aalseth, C.; Bailey, V. L.; Mace, E. K.; Overman, C.; Seifert, A.; Wilcox Freeburg, E. D.

2015-12-01

Tritium (T) measurements offer insight to a wealth of environmental applications including hydrologic tracking, discerning ocean circulation patterns, and aging ice formations. However, the relatively short half-life of T (12.3 years) limits its effective age dating range. Compounding this limitation is the decrease in atmospheric T content by over two orders of magnitude (from 1000-2000 TU in 1962 to testing in the 1960's. We are developing sample preparation methods coupled to direct counting of T via ultra-low background proportional counters which, when combined, offer improved T measurement sensitivity (~4.5 mmoles of H2 equivalent) and will help expand the application of T age dating to smaller sample sizes linked to persistent environmental questions despite the limitations above. For instance, this approach can be used to T date ~ 2.2 mmoles of CH4 collected from sample-limited systems including microbial communities, soils, or subsurface aquifers and can be combined with radiocarbon dating to distinguish the methane's formation age from C age in a system. This approach can also expand investigations into soil organic C where the improved sensitivity will permit resolution of soil C into more descriptive fractions and provide direct assessments of the stability of specific classes of organic matter in soils environments. We are employing a multiple step sample preparation system whereby organic samples are first combusted with resulting CO2 and H2O being used as a feedstock to synthesize CH4. This CH4 is mixed with Ar and loaded directly into an ultra-low background proportional counter for measurement of T β decay in a shallow underground laboratory. Analysis of water samples requires only the addition of geologic CO2 feedstock with the sample for methane synthesis. The chemical nature of the preparation techniques enable high sample throughput with only the final measurement requiring T decay with total sample analysis time ranging from 2 -5 weeks

Evaluation of environmental samples containing heavy hydrocarbon components in environmental forensic investigations

Energy Technology Data Exchange (ETDEWEB)

Raia, J.C.; Blakley, C.R.; Fuex, A.N.; Villalanti, D.C.; Fahrenthold, P.D. [Triton Anal Corp, Houston, TX (United States)

2004-03-01

This article presents a procedure to evaluate and characterize environmental samples containing mixtures of hydrocarbons over a wide boiling range of materials that include fuels and other products used in commerce. The range of the method extends to the higher boiling and heavier molecular weight hydrocarbon products in the range of motor oil, bunker fuel, and heavier residue materials. The procedure uses the analytical laboratory technique of high-temperature simulated distillation along with mathematical regression of the analytical data to estimate the relative contribution of individual products in mixtures of hydrocarbons present in environmental samples. An analytical technique to determine hydrocarbon-type distributions by gas chromatography-mass spectrometry with nitric oxide ionization spectrometry evaluation is also presented. This type of analysis allows complex hydrocarbon mixtures to be classified by their chemical composition, or types of hydrocarbons that include paraffins, cycloparaffins, monoaromatics, and polycyclic aromatic hydrocarbons. Characteristic hydrocarbon patterns for example, in the relative distribution of polycyclic aromatic hydrocarbons are valuable for determining the potential origin of materials present in environmental samples. These methods provide quantitative data for hydrocarbon components in mixtures as a function of boiling range and 'hydrocarbon fingerprints' of the types of materials present. This information is valuable in assessing environmental impacts of hydrocarbons at contaminated sites and establishing the liabilities and cost allocations for responsible parties.

Middlesex Sampling Plant: Annual environmental report for calendar year 1990, Middlesex, New Jersey

International Nuclear Information System (INIS)

1991-09-01

Environmental monitoring of the US Department of Energy's (DOE) Middlesex Sampling Plant (MSP) and surrounding area began in 1980. MSP is part of the Formerly Utilized Sites Remedial Action Program (FUSRAP), a DOE program to decontaminate or otherwise control sites where residual radioactive materials remain from the early years of the nation's atomic energy program or from commercial operations causing conditions that Congress has authorized DOE to remedy. The environmental monitoring program at MSP includes sampling networks for radon concentrations in air; external gamma radiation exposure; and radium-226, thorium-232, and total uranium concentrations in surface water, sediment, and groundwater. Additionally, several nonradiological parameters were measured in groundwater, surface water, and sediment. 14 refs., 17 figs., 29 tabs

Analysis of polychlorinated n-alkanes in environmental samples.

Science.gov (United States)

Santos, F J; Parera, J; Galceran, M T

2006-10-01

Polychlorinated n-alkanes (PCAs), also known as chlorinated paraffins (CPs), are highly complex technical mixtures that contain a huge number of structural isomers, theoretically more than 10,000 diastereomers and enantiomers. As a consequence of their persistence, tendency to bioaccumulation, and widespread and unrestricted use, PCAs have been found in aquatic and terrestrial food webs, even in rural and remote areas. Recently, these compounds have been included in regulatory programs of several international organizations, including the US Environmental Protection Agency and the European Union. Consequently, there is a growing demand for reliable methods with which to analyze PCAs in environmental samples. Here, we review current trends and recent developments in the analysis of PCAs in environmental samples such as air, water, sediment, and biota. Practical aspects of sample preparation, chromatographic separation, and detection are covered, with special emphasis placed on analysis of PCAs using gas chromatography-mass spectrometry. The advantages and limitations of these techniques as well as recent improvements in quantification procedures are discussed.

Environmental sampling accounting at the Savannah River Plant

International Nuclear Information System (INIS)

Zeigler, C.C.; Wood, M.B.

1978-06-01

At the Savannah River Plant Environmental Monitoring Laboratories, a computer-based systematic accounting method was developed to ensure that all scheduled samples are collected, processed through the laboratory, and counted without delay. The system employs an IBM 360/195 computer with a magnetic tape master file, an on-line disk file, and cathode ray tube (CRT) terminals. Scheduling and accounting are accomplished by using computer-generated schedules, collection labels, and output/input cards. For each scheduled sample and analysis, a printed card is issued for collection, laboratory analysis, and counting. The cards also contain information needed by personnel performing the jobs, such as sample location, aliquot to be processed, or procedure number. Manual entries are made on the cards when each step in the process is completed. Additional pertinent data are also manually entered on the cards; e.g., entries are made explaining why a sample is not collected, the sample aliquot in the event a nonstandard aliquot is processed, field measurement results, and analytical results. These manually entered data are keypunched and read into the computer files. The computer files are audited daily, and summaries of samples not processed in pre-established normal time intervals are issued. The progress of sample analyses can also be readily determined at any time using the CRT terminal. Historic data are also maintained on magnetic tape and workload summaries are issued showing the number of samples and number of determinations per month

Determination of 36Cl in environmental samples collected in the JCO by AMS

International Nuclear Information System (INIS)

Seki, R.; Tsukuba Univ., Ibaraki; Arai, D.; Nagashima, Y.; Takahashi, T.; Matsuhiro, T.; Imanaka, T.

2003-01-01

Long-lived chlorine, 36 Cl (T 1/2 = 301,000 y) in environmental samples has been measured by the AMS system installed in Tandem Accelerator Center, University of Tsukuba. A tri-carbon-molecular 12 C 3 - pilot beam method is used to stabilize the terminal voltage of the tandem. A small amount of pure carbon graphite is well mixed into a AgCl target material for creating Cl - and 12 C 3 - in the ion source. A 36 S isobaric interference in the system is eliminated to determine 36 Cl in environmental samples by chemical procedure. Some samples containing chlorine such as soil, chemical reagents and table salt have been collected in the JCO criticality accident site and analyzed to detect neutron-induced 36 Cl. The experimental result has been compared with a theoretical calculation. (author)

Political measures for promoting environmental technology

International Nuclear Information System (INIS)

2006-01-01

Environmental technology can contribute to solving many environmental challenges and to industrial development. Measures to support the development and use of such technologies can be regulatory, economic or administrative, and usually one needs to use a combination of different measures in order to reach both a better environment and industrial development. For industrial development other measures than those administered by environmental authorities will be of importance. The environmental authorities therefore need to acquire knowledge about these measures and the bodies administering them, and develop an operative cooperation with these actors

Environmental Measurements and Modeling

Science.gov (United States)

Environmental measurement is any data collection activity involving the assessment of chemical, physical, or biological factors in the environment which affect human health. Learn more about these programs and tools that aid in environmental decisions

Direct separation of plutonium by thermochromatography from environmental samples

International Nuclear Information System (INIS)

Wacker, L.; Kraehenbuehl, U.

2002-01-01

A thermochromatographic separation was performed on plutonium from environmental soil samples. This procedure was investigated with the goal to measure low concentrations of plutonium by inductively coupled plasma-mass spectrometry (ICP-MS). The soil sample was chlorinated by thionylchloride as reactive gas at a temperature of 1400 K. The volatile chlorides were separated chromatographically and deposited in a temperature gradient tube filled with quartz grains. Results about the deposition behaviour of the elements were obtained. Two different formalisms based on the thermodynamic functions are used to describe the experimental data. One formula is used to describe the deposition behaviour of microscopic amounts of plutonium (adsorption), the other formula for macroamounts of the main matrix elements (desublimation). The calculated values are in a reasonable agreement with the experimental data. A determination of plutonium content was successfully made for a referenced sea sediment (IAEA-135) after the thermochromatographic sample preparation for ICP-MS. (orig.)

Progress in the methods for analyses and measurements of environmental radionuclides

International Nuclear Information System (INIS)

1984-01-01

The tenth seminar on environment of the National Institute of Radiological Sciences was held in Chiba on December 9 and 10, 1982, under the joint auspices with Japan Health Physics Society. The recent progress of the measuring techniques for environmental radiation substances is remarkable. The Japanese data on environmental radiation presented to the UN Scientific Committee on the Effect of Atomic Radiation have obtained very high esteem because the data have been reliable due to the progress of measuring techniques. However, this field is in steady progress and changes rapidly, therefore, this seminar was planned. In this report, the history of the analysis and measurement of environmental radioactivity, the method of sampling and pretreatment operation for such environmental specimens as gaseous radionuclides, atmospheric floating dust, soil, agricultural products, sea water and sea bottom sediment, marine life, foods and living bodies, the progress of chemical separation process, the automation of analysis and measurement, the progress of the analysis of low level nuclides with long half-value period, the manual for the analysis and measurement, the quality of the analysis and measurement and its assurance are described. (Kako, I.)

o-TOF ICPMS analysis of environmental, food and biological samples

International Nuclear Information System (INIS)

Krejcova, A.; Cernohorsky, T.; Ludvikova, I.; Pouzar, M.; Capova, L.

2009-01-01

Full text: o-TOF ICPMS was used for inorganic analysis of environmental, food and biological samples. The method validity was proved by analysis of spiked samples, reference materials, by determination without/with internal standards and the standard addition technique. The technique was shown to be powerful, and reliable for analysis of the samples mentioned, and high sample throughput enables environmental or biological screening studies. Independent of the number of elements analyzed, complete analysis and whole mass spectra are gained from a small sample amount in a very short time. (author)

Measurement of environmental tritium for isotope hydrology studies

International Nuclear Information System (INIS)

1973-01-01

The Section of Isotope Hydrology of the IAEA Division of Research and Laboratories gains valuable hydrological information from studies of the concentration of environmental tritium in precipitation, surface and groundwater samples from various sites around the world. This photo story shows the steps in the measurement of these very low levels of tritium in water as performed in the Isotope Hydrology Laboratory of the Agency. (author)

Influence of short-term sampling parameters on the uncertainty of the Lden environmental noise indicator

International Nuclear Information System (INIS)

Mateus, M; Carrilho, J Dias; Da Silva, M Gameiro

2015-01-01

The present study deals with the influence of the sampling parameters on the uncertainty of noise equivalent level in environmental noise measurements. The study has been carried out through the test of different sampling strategies doing resampling trials over continuous monitoring noise files obtained previously in an urban location in the city of Coimbra, in Portugal. On short term measurements, not only the duration of the sampling episodes but also its number have influence on the uncertainty of the result. This influence is higher for the time periods where sound levels suffer a greater variation, such as during the night period. In this period, in case both parameters (duration and number of sampling episodes) are not carefully selected, the uncertainty level can reach too high values contributing to a loss of precision of the measurements. With the obtained data it was investigated the sampling parameters influence on the long term noise indicator uncertainty, calculated according the Draft 1st CD ISO 1996-2:2012 proposed method. It has been verified that this method allows the possibility of defining a general methodology which enables the setting of the parameters once the precision level is fixed. For the three reference periods defined for environmental noise (day, evening and night), it was possible to derive a two variable power law representing the uncertainty of the determined values as a function of the two sampling parameters: duration of sampling episode and number of episodes

Environmental radiation measurements using lithium fluoride thermoluminescence dosemeters

Energy Technology Data Exchange (ETDEWEB)

Driscoll, C.M.H.; Green, B.M.R.; McKinlay, A.F.; Richards, D.J. (National Radiological Protection Board, Harwell (UK))

1984-01-01

The National Radiological Protection Board is involved in a large scale environmental survey of radiation levels in homes throughout the United Kingdom. Passive radon and gamma ray dosemeters are posted to a representative sample of households. Lithium fluoride thermoluminescence dosemeters are used to assess natural gamma radiation and are left in the measurement location for a period of six months before being returned to the Board for processing. As a preliminary to the national survey, the Board has been engaged on several limited surveys in regions of igneous and sedimentary geology. Experience gained in these limited surveys and from standardisation studies using environmental dosemeters are reported.

Hanford Site Environmental Surveillance Master Sampling Schedule for Calendar Year 2006

Energy Technology Data Exchange (ETDEWEB)

Bisping, Lynn E.

2006-01-27

This document contains the calendar year 2006 schedules for the routine and non-routine collection of samples for the Surface Environmental Surveillance Project (SESP) and Drinking Water Monitoring Project. Each section includes sampling locations, sample types, and analyses to be performed. In some cases, samples are scheduled on a rotating basis and may not be collected in 2006 in which case the anticipated year for collection is provided. The project document package (PDP) for Surface Environmental Surveillance contains the milestone control log for the issuing of CY06 Environmental Surveillance Master Sampling Schedule WBS 4.2.3.21.3.03, milestone: RL00430306 (4830106-12).

Transuranium analysis methodologies for biological and environmental samples

International Nuclear Information System (INIS)

Wessman, R.A.; Lee, K.D.; Curry, B.; Leventhal, L.

1978-01-01

Analytical procedures for the most abundant transuranium nuclides in the environment (i.e., plutonium and, to a lesser extent, americium) are available. There is a lack of procedures for doing sequential analysis for Np, Pu, Am, and Cm in environmental samples, primarily because of current emphasis on Pu and Am. Reprocessing requirements and waste disposal connected with the fuel cycle indicate that neptunium and curium must be considered in environmental radioactive assessments. Therefore it was necessary to develop procedures that determine all four of these radionuclides in the environment. The state of the art of transuranium analysis methodology as applied to environmental samples is discussed relative to different sample sources, such as soil, vegetation, air, water, and animals. Isotope-dilution analysis with 243 Am ( 239 Np) and 236 Pu or 242 Pu radionuclide tracers is used. Americium and curium are analyzed as a group, with 243 Am as the tracer. Sequential extraction procedures employing bis(2-ethyl-hexyl)orthophosphoric acid (HDEHP) were found to result in lower yields and higher Am--Cm fractionation than ion-exchange methods

Sampling artifacts in measurement of elemental and organic carbon: Low-volume sampling in indoor and outdoor environments

Science.gov (United States)

Olson, David A.; Norris, Gary A.

Experiments were completed to determine the extent of artifacts from sampling elemental carbon (EC) and organic carbon (OC) under sample conditions consistent with personal sampling. Two different types of experiments were completed; the first examined possible artifacts from oils used in personal environmental monitor (PEM) impactor plates, and the second examined artifacts from microenvironmental sampling using different sampling media combinations (quartz, Teflon, XAD denuder, and electrostatic precipitator). The effectiveness of front and backup filters was evaluated for most sampling configurations. Mean total carbon concentrations from sampling configurations using impactor oils were not statistically different from the control case (using a sharp cut cyclone). Three microenvironments were tested (kitchen, library, and ambient); carbon concentrations were highest in the kitchen using a front quartz filter (mean OC of 16.4 μg m -3). The lowest front quartz filter concentrations were measured in the library using XAD denuders (mean OC of 3.6 μg m -3). Denuder removal efficiencies (average of 82% for total carbon) were lower compared with previous ambient studies and may indicate that indoor sources influenced denuder efficiency during sample collection. The highest carbon concentrations from backup quartz filters were measured using the Teflon-quartz combination.

Environmental monitoring master sampling schedule: January--December 1989

International Nuclear Information System (INIS)

Bisping, L.E.

1989-01-01

Environmental monitoring of the Hanford Site is conducted by the Pacific Northwest Laboratory (PNL) for the US Department of Energy (DOE). This document contains the planned schedule for routine sample collection for calendar year 1989 for the Surface and Ground-Water Environmental Monitoring Projects. This schedule is subject to modification during the year in response to changes in Site operations, program requirements, and the nature of the observed results. Operational limitations such as weather, mechanical failures, sample availability, etc., may also require schedule modifications. Changes will be documented in the respective project files, but this plan will not be reissued. This schedule includes routine ground-water sampling performed by PNL for Westinghouse Hanford Company, but does not include samples that may be collected in 1989 to support special studies or special contractor projects, or for quality control. The sampling schedule for Site-wide chemical monitoring is not included here, because it varies each quarter as needed, based on past results and operating needs. This schedule does not include Resource Conservation and Recovery Act ground-water sampling performed by PNL for Hanford Site contractors, nor does it include sampling that may be done by other DOE Hanford contractors

Determination of 90Sr in environmental samples with resonance ionization spectroscopy in collinear geometry

International Nuclear Information System (INIS)

Zimmer, K.; Stenner, J.; Kluge, H.J.; Lantzsch, J.; Monz, L.; Otten, E.W.; Passler, G.; Schwalbach, R.; Schwarz, M.; Stevens, H.; Wendt, K.; Herrmann, G.; Niess, S.; Trautmann, N.; Walter, K.; Bushaw, B.A.

1994-01-01

A new, fast technique for trace analysis of the radioactive isotopes 89 Sr and 90 Sr in environmental samples has been developed. Conventional mass separation is combined with resonance ionization spectroscopy in collinear geometry, which provides high selectivity and sensitivity. In addition, a chemical separation procedure for sample preparation has been developed. The described technique was used to determine the 90 Sr content in ∼ 870 m 3 air samples collected near Munich during and shortly after the Chernobyl reactor accident in April 1986. The content of 90 Sr was measured to be 1.4 mBq per m 3 , corresponding to 1.6 x 10 9 atoms of 90 Sr per sample. This value is in good agreement with the results of radiochemical measurements. (orig.)

A study on antimony determination in environmental samples by neutron activation analysis: validation of the methodology and determination of the uncertainty of the measurement

International Nuclear Information System (INIS)

Matsubara, Tassiane Cristina Martins

2011-01-01

Antimony is an element found in low concentrations in the environment. However, its determination has attracted great interest due to the knowledge of its toxicity and increasing application in industry. The determination of antimony has been a challenge for researchers since this element is found in low concentrations which make its analysis a difficult task. Therefore, although neutron activation analysis (NAA) is an appropriate method for the determination of various elements in different types of matrix, in the case of Sb its analysis presents some difficulties, mainly due to spectral interferences. The objective of this research was to validate the NAA method for Sb determination in environmental samples. To establish appropriate conditions for Sb determinations, preliminary assays were carried out for further analysis of certified reference materials (CRM). The experimental procedure was to irradiate samples with a synthetic Sb standard for a period of 8 or 16 hours in the IEA-R1 nuclear research reactor, followed by gamma ray spectrometry. The quantification of Sb was performed by measuring the radioactive isotopes of 122 Sb and '1 24 Sb. The results of preliminary assays indicated the presence of Sb in Whatman no 40 filter paper used in the preparation of the synthetic standard, but at very low concentrations, which could be considered negligible. In the case of the plastic material used in bags for the sample irradiation, it should be chosen carefully, because depending on the thickness, they may contain Sb. The analyses of the stability of the diluted Sb standard solution showed no change in the Sb concentration within eight months after its preparation. Results obtained in the analysis of certified reference materials indicated the interference of 76 As and also of 134 Cs and 152 Eu in the Sb determinations by measuring '1 22 Sb, due to the proximity of the gamma ray energies. The high activity of '2 4 Na can also mask the peak of 122 Sb hindering its

Environmental monitoring master sampling schedule, January--December 1990

Energy Technology Data Exchange (ETDEWEB)

Bisping, L.E.

1990-01-01

Environmental monitoring of the Hanford Site is conducted by the Pacific Northwest Laboratory (PNL) for the US Department of Energy (DOE). This document contains the planned schedule for routine sample collection for calendar year 1990 for the Environment Surveillance and Ground-Water Monitoring Projects. This schedule is subject to modification during the year in response to changes in Site operations, program requirements, and the nature of the observed results. Operational limitations such as weather, mechanical failures, sample availability, etc., may also require schedule modifications. Changes will be documented in the respective project files, but this plan will not be reissued. The purpose of these monitoring projects is to evaluate levels of radioactive and nonradioactive pollutants in the Hanford environs. This schedule includes ground-water sampling performed by PNL for environmental surveillance of the Hanford Site.

ICP-MS measurements of iodine and bromine in environmental samples collected along the Kuji River, Japan

International Nuclear Information System (INIS)

Kushita, Kouhei N.; Amano, Hikaru

2003-01-01

From a viewpoint of monitoring the distribution and transfer of long-lived radioiodine ( 129 I) and possible hazardous brominated substances, I and Br contents in various environmental samples collected in the Kuji River area, Japan, were studied by ICP-MS. The feature of the change in concentrations of I and Br, as well as those of other general properties such as pH etc., in Kuji River watershed were coincident with each other. It is considered from the obtained data that the environmental conditions, especially those of the soil of the area, mainly control the distribution of I and Br in the river water. The circulation characteristics of I and Br showed different features in different transfer media, which could be ascribed to the different chemical properties of these elements in each media. It was also shown that the distributions of I and Br are varied even within a small zone of about 20 km width around a high mountain of this area, which is also considered to reflect the environmental characteristics of the district. (author)

A new measurement method for quantification and speciation of technetium-99 in sample at environmental concentrations

International Nuclear Information System (INIS)

Kasprzak, L.M.; Aubert, C.; Cossonnet, C.; Fattahi, M.

2006-01-01

Technetium-99 is a pure β- emitter and important long half-lived multi-valent radionuclide to be considered in radiation protection of the environment and the public. It a fission product of both 235 U and 239 Pu with approximately a 6% yield. The most stable and very mobile form of Tc is the pertechnetate anion (TcO 4 - ). Therefore, environmental monitoring requires the knowledge of the redox and chemical properties of this element in order to predict its behaviour and transfer in the environment. Given the extremely low concentration of 99 Tc in the environment (10 -10 M to 10 -12 M), its determination currently necessitates an enrichment and separation from the sample matrix prior to instrumental measurement. To this end, the development of a suitable analytical technique is required. The advantages of Capillary Electrophoresis (CE) as a powerful separation technique can be combined with the atomic specificity, multi-elemental character and extremely high sensitivity of an inductively coupled plasma mass spectrometer (ICP-MS) for trace metal-speciation studies in different fields of interest. However, the coupling of both commercially available instruments deserves particular attention if separative resolution, high analyte transport efficiency and sensitive detection are to be achieved. In, that technical vein, the interface itself may be considered as the 'key to success'. Several attempts to develop interfaces for CE-ICP-MS have been described over the last few years. However, the 99 Tc quantification by ICP-MS can be disturbed by isobaric overlaps 99 Ru and interferences induced by the matrix, including those associated with hydride formation ( 98 Mo 1 H (23.8%), 98 Ru 1 H (1.9%)). The aim of the present study was to develop a rapid and efficient method for the determination of 99 Tc in environmental samples by CE-ICP-MS without preliminary classical radiochemical separation to eliminate the interfering elements. In this paper, we describe the development

Environmental Audit of the Environmental Measurements Laboratory (EML)

International Nuclear Information System (INIS)

1992-02-01

This document contains the findings identified during the Environmental Audit of the Environmental Measurements Laboratory (EML), conducted from December 2 to 13, 1991. The Audit included the EML facility located in a fifth-floor General Services Administration (GSA) office building located in New York City, and a remote environmental monitoring station located in Chester, New Jersey. The scope of this Environmental Audit was comprehensive, covering all areas of environmental activities and waste management operations, with the exception of the National Environmental Policy Act (NEPA), which is the responsibility of the DOE Headquarters Office of NEPA Oversight. Compliance with applicable Federal, state, and local requirements; applicable DOE Orders; and internal facility requirements was addressed

Environmental sampling: Issues for the cut-off regime

International Nuclear Information System (INIS)

Fearey, B.L.

1995-01-01

The fissile material cut-off treaty (FMCT) initiative under the Conference on Disarmament mandate is envisioned to include certain aspects of environmental sampling and monitoring. One of the intents of this treaty is to bring certain non-NPT signatories (e.g., threshold states) under this treaty agreement along with the nuclear weapon states (NWSs). This paper provides a brief overview of some of the relevant issues that may be involved in the implementation and use of environmental monitoring for (1) verification of the cut-off regime declarations, (2) the detection of undeclared activities, and, (3) application in non-routine inspections. The intent is to provide backstopping information important for treaty negotiators. Specific issues addressed within this paper include signature sampling, differences in the proposed detection regime, potential signature integrators, specific examples and spoofing concerns. Many of these issues must be carefully considered and weighed in order to create a credibly verifiable inspection regime. Importantly, the cut-off treaty must enable nondiscriminatory implementation, while carefully assuring that nonproliferation treaty requirements are maintained (i.e., preventing unintentional release of critical weapons design information--potentially through environmental sampling and analysis)

Use of Statistics for Data Evaluation in Environmental Radioactivity Measurements

International Nuclear Information System (INIS)

Sutarman

2001-01-01

Counting statistics will give a correction on environmental radioactivity measurement result. Statistics provides formulas to determine standard deviation (S B ) and minimum detectable concentration (MDC) according to the Poisson distribution. Both formulas depend on the background count rate, counting time, counting efficiency, gamma intensity, and sample size. A long time background counting results in relatively low S B and MDC that can present relatively accurate measurement results. (author)

Middlesex Sampling Plant annual environmental report for calendar year 1991, Middlesex, New Jersey

International Nuclear Information System (INIS)

1992-09-01

This document describes the environmental monitoring program at the-Middlesex Sampling Plant (MSP) and surrounding area, implementation of the program, and monitoring results for 1991. Environmental monitoring of MSP began in 1980 when Congress added the site to the US Department of Energy's (DOE) Formerly Utilized Sites Remedial Action Program (FUSRAP). FUSRAP is a DOE program to decontaminate or otherwise control sites where residual radioactive materials remain from the early years of the nation's atomic energy program or from commercial operations causing conditions that Congress has authorized DOE to remedy. The environmental monitoring program at MSP includes sampling networks for radon and thoron concentrations in air; external gamma radiation exposure; and radium-226, thorium-232, and total uranium concentrations in surface water, sediment,, and groundwater. Additionally, several nonradiological parameters are measured in groundwater, surface water, and sediment. Results of environmental monitoring during 1991 indicate that most concentrations were well below applicable guidelines. The potential radiation dose calculated for a hypothetical maximally exposed individual, based on a conservative but realistic exposure scenario, is 2.3 mrem (milliroentgen equivalent man) per year, which is less than an individual would receive while traveling in an airplane at 12,000 meters for five hours. During 1991, there were no nonroutine releases from the site; MSP was in compliance with applicable regulations for releases from the site. Site activities included environmental monitoring, site maintenance, onsite characterization for the MSP remedial investigation, and additional sediment sampling at the plant outfall to determine the source of the elevated levels of radium-226 and thorium-232

[DOE method for evaluating environmental and waste management samples: Revision 1, Addendum 1

Energy Technology Data Exchange (ETDEWEB)

Goheen, S.C.

1995-04-01

The US Dapartment of Energy`s (DOE`s) environmental and waste management (EM) sampling and analysis activities require that large numbers of samples be analyzed for materials characterization, environmental surveillance, and site-remediation programs. The present document, DOE Methods for Evaluating Environmental and Waste Management Samples (DOE Methods), is a supplemental resource for analyzing many of these samples.

[DOE method for evaluating environmental and waste management samples: Revision 1, Addendum 1

International Nuclear Information System (INIS)

Goheen, S.C.

1995-04-01

The US Dapartment of Energy's (DOE's) environmental and waste management (EM) sampling and analysis activities require that large numbers of samples be analyzed for materials characterization, environmental surveillance, and site-remediation programs. The present document, DOE Methods for Evaluating Environmental and Waste Management Samples (DOE Methods), is a supplemental resource for analyzing many of these samples

Self-attenuation of gamma rays during radioactivity concentration analysis of environmental samples

International Nuclear Information System (INIS)

Watson, D.; Dharmasiri, J.; Akber, R.

2001-01-01

Gamma spectroscopy using HPGe detector systems is a readily used technique for routine analysis of radioactivity in environmental samples. The systems are generally calibrated using standards of known radioactivity and composition. Radioactivity in environmental samples is generally distributed in the bulk of the material. When a sample of finite thickness is analysed through gamma spectroscopy, a proportion of the gamma rays emitted from the sample is either stopped or scattered from the sample material itself. These processes of self-absorption and self-attenuation depend upon the physical and elemental composition of the sample and the energy of the gamma radiation. Since environmental samples vary in composition, instrument calibration using a fixed matrix composition may not be valid for a diversity of samples. We selected and analysed five sample matrices to investigate the influence of self-absorption and self-attenuation in environmental samples. Our selection consisted of bentonite and kaolin representing clay, quartz representing silica, ash representing prepared biota, and analytical grade MnO 2 representing a co-precipitant used for extractive radioactivity from aqueous samples. Our findings show that within 5% of uncertainty the silica based standards can be used to cover the environmental samples of varying clay (silica content). The detection efficiency for ash and MnO 2 could be different particularly in the 30 - 100 keV energy range. The differences in sample behaviour can be explained on the basis of atomic number, mass number and density

Detection and Molecular Characterization of Gemycircularvirus from Environmental Samples in Brazil.

Science.gov (United States)

da Silva Assis, Matheus Ribeiro; Vieira, Carmen Baur; Fioretti, Julia Monassa; Rocha, Mônica Simões; de Almeida, Pedro Ivo Neves; Miagostovich, Marize Pereira; Fumian, Tulio Machado

2016-12-01

Gemycircularvirus (GemyCV) is a group of viruses which has been recently proposed as a new viral genus detected in fecal and environmental samples around the world. GemyCVs have been detected in human blood, brain tissue, cerebrospinal fluid, and stool sample. In the present study, we demonstrate for the first time, through molecular detection and characterization, the presence of GemyCVs in environmental samples from Brazil. Our results show a percentage of positivity ranging from 69 (25/36) to 97 % (35/36) in river water samples collected in Manaus, Amazon region, and wastewater from a wastewater treatment plant located in Rio de Janeiro, respectively, revealing GemyCVs as an important environmental contaminant.

DOE methods for evaluating environmental and waste management samples

International Nuclear Information System (INIS)

Goheen, S.C.; McCulloch, M.; Thomas, B.L.; Riley, R.G.; Sklarew, D.S.; Mong, G.M.; Fadeff, S.K.

1994-04-01

DOE Methods for Evaluating Environmental and Waste Management Samples (DOE Methods) is a resource intended to support sampling and analytical activities for the evaluation of environmental and waste management samples from U.S. Department of Energy (DOE) sites. DOE Methods is the result of extensive cooperation from all DOE analytical laboratories. All of these laboratories have contributed key information and provided technical reviews as well as significant moral support leading to the success of this document. DOE Methods is designed to encompass methods for collecting representative samples and for determining the radioisotope activity and organic and inorganic composition of a sample. These determinations will aid in defining the type and breadth of contamination and thus determine the extent of environmental restoration or waste management actions needed, as defined by the DOE, the U.S. Environmental Protection Agency, or others. The development of DOE Methods is supported by the Laboratory Management Division of the DOE. Methods are prepared for entry into DOE Methods as chapter editors, together with DOE and other participants in this program, identify analytical and sampling method needs. Unique methods or methods consolidated from similar procedures in the DOE Procedures Database are selected for potential inclusion in this document. Initial selection is based largely on DOE needs and procedure applicability and completeness. Methods appearing in this document are one of two types. open-quotes Draftclose quotes or open-quotes Verified.close quotes. open-quotes Draftclose quotes methods that have been reviewed internally and show potential for eventual verification are included in this document, but they have not been reviewed externally, and their precision and bias may not be known. open-quotes Verifiedclose quotes methods in DOE Methods have been reviewed by volunteers from various DOE sites and private corporations

Code Betal to calculation Alpha/Beta activities in environmental samples

International Nuclear Information System (INIS)

Romero, L.; Travesi, A.

1983-01-01

A codes, BETAL, was developed, written in FORTRAN IV, to automatize calculations and presentations of the result of the total alpha-beta activities measurements in environmental samples. This code performs the necessary calculations for transformation the activities measured in total counts, to pCi/1., bearing in mind the efficiency of the detector used and the other necessary parameters. Further more, it appraise the standard deviation of the result, and calculus the Lower limit of detection for each measurement. This code is written in iterative way by screen-operator dialogue, and asking the necessary data to perform the calculation of the activity in each case by a screen label. The code could be executed through any screen and keyboard terminal, (whose computer accepts Fortran IV) with a printer connected to the said computer. (Author) 5 refs

The procedures manual of the Environmental Measurements Laboratory. Volume 1, 28. edition

Energy Technology Data Exchange (ETDEWEB)

Chieco, N.A. [ed.

1997-02-01

This manual covers procedures and technology currently in use at the Environmental Measurements Laboratory. An attempt is made to be sure that all work carried out will be of the highest quality. Attention is focused on the following areas: quality assurance; sampling; radiation measurements; analytical chemistry; radionuclide data; special facilities; and specifications.

The procedures manual of the Environmental Measurements Laboratory. Volume 1, 28. edition

International Nuclear Information System (INIS)

Chieco, N.A.

1997-02-01

This manual covers procedures and technology currently in use at the Environmental Measurements Laboratory. An attempt is made to be sure that all work carried out will be of the highest quality. Attention is focused on the following areas: quality assurance; sampling; radiation measurements; analytical chemistry; radionuclide data; special facilities; and specifications

How to take environmental samples for stable isotope analyses

International Nuclear Information System (INIS)

Rogers, K.M.

2009-01-01

It is possible to analyse a diverse range of samples for environmental investigations. The main types are soil/sediments, vegetation, fauna, shellfish, waste and water. Each type of samples requires different storage and collection methods. Outlined here are the preferred methods of collection to ensure maximum sample integrity and reliability. (author).

How to take environmental samples for stable isotope analyses

International Nuclear Information System (INIS)

Rogers, K.M.

2013-01-01

It is possible to analyse a diverse range of samples for environmental investigations. The main types are soil/sediments, vegetation, fauna, shellfish, waste and water. Each type of samples requires different storage and collection methods. Outlined here are the preferred methods of collection to ensure maximum sample integrity and reliability. (author).

How to take environmental samples for stable isotope analyses

International Nuclear Information System (INIS)

Rogers, K.M.

2012-01-01

It is possible to analyse a diverse range of samples for environmental investigations. The main types are soil/sediments, vegetation, fauna, shellfish, waste and water. Each type of samples requires different storage and collection methods. Outlined here are the preferred methods of collection to ensure maximum sample integrity and reliability. (author).

How to take environmental samples for stable isotope analyses

International Nuclear Information System (INIS)

Rogers, K.M.

2009-01-01

It is possible to analyse a diverse range of samples for environmental investigations. The main types are soil/sediments, vegetation, fauna, shellfish, waste and water. Each type of samples requires different storage and collection methods. Outlined here are the preferred methods of collection to ensure maximum sample integrity and reliability. (author)

Least-squares resolution of gamma-ray spectra in environmental samples

International Nuclear Information System (INIS)

Kanipe, L.G.; Seale, S.K.; Liggett, W.S.

1977-08-01

The use of ALPHA-M, a least squares computer program for analyzing NaI (Tl) gamma spectra of environmental samples, is evaluated. Included is a comprehensive set of program instructions, listings, and flowcharts. Two other programs, GEN4 and SIMSPEC, are also described. GEN4 is used to create standard libraries for ALPHA-M, and SIMSPEC is used to simulate spectra for ALPHA-M analysis. Tests to evaluate the standard libraries selected for use in analyzing environmental samples are provided. An evaluation of the results of sample analyses is discussed

Determination of technetium-99 in environmental and radioactive waste samples

International Nuclear Information System (INIS)

Ferencova, M.; Peter Tkac, P.

2007-01-01

Technetium is known for its high mobility in a soil-water system in non-reducing aerobic condition and also high bio-availability for plants, because the most stable form of technetium in natural surface environment is pertechnetate which is highly soluble. The chemical form of technetium changes with environmental conditions. Concentration of technetium in the environment is very low, therefore many separation steps are needed for technetium determination. It has been developed a method for the routine determination of technetium-99 from environmental matrices and radioactive wastes using technetium-99m as an internal yield monitor. Technetium-99 is extracted from the soil samples with nitric acid. Many contaminants are co-precipitated with ferric hydroxide and technetium in the supernatant is pre-concentrated and further purified using anion exchange chromatography. Final separation of technetium was achieved by extraction with tetraphenylarsonium chloride in chloroform from sulphuric acid or pure water. The chemical yield is determined through the measurement of technetium-99m by scintillation counting system and the technetium-99 activity is measured using proportional counter after decay of the technetium-99m activity. Typical recoveries for this method are in the order 50-60 % (authors)

AAS determination of total mercury content in environmental samples

International Nuclear Information System (INIS)

Moskalova, M.; Zemberyova, M.

1997-01-01

Two methods for determination of total mercury content in environmental samples soils, and sediments, were compared. Dissolution procedure of soils, sediments, and biological material under elevated pressure followed by determination of mercury by cold vapour atomic absorption spectrometry using a MHS-1 system and direct total mercury determination without any chemical pretreatment from soil samples using a Trace Mercury Analyzer TMA-254 were compared. TMA-254 was also applied for the determination of mercury in various further standard reference materials. Good agreement with certified values of environmental reference materials was obtained. (authors)

Estimation of Uncertainty in Aerosol Concentration Measured by Aerosol Sampling System

Energy Technology Data Exchange (ETDEWEB)

Lee, Jong Chan; Song, Yong Jae; Jung, Woo Young; Lee, Hyun Chul; Kim, Gyu Tae; Lee, Doo Yong [FNC Technology Co., Yongin (Korea, Republic of)

2016-10-15

FNC Technology Co., Ltd has been developed test facilities for the aerosol generation, mixing, sampling and measurement under high pressure and high temperature conditions. The aerosol generation system is connected to the aerosol mixing system which injects SiO{sub 2}/ethanol mixture. In the sampling system, glass fiber membrane filter has been used to measure average mass concentration. Based on the experimental results using main carrier gas of steam and air mixture, the uncertainty estimation of the sampled aerosol concentration was performed by applying Gaussian error propagation law. FNC Technology Co., Ltd. has been developed the experimental facilities for the aerosol measurement under high pressure and high temperature. The purpose of the tests is to develop commercial test module for aerosol generation, mixing and sampling system applicable to environmental industry and safety related system in nuclear power plant. For the uncertainty calculation of aerosol concentration, the value of the sampled aerosol concentration is not measured directly, but must be calculated from other quantities. The uncertainty of the sampled aerosol concentration is a function of flow rates of air and steam, sampled mass, sampling time, condensed steam mass and its absolute errors. These variables propagate to the combination of variables in the function. Using operating parameters and its single errors from the aerosol test cases performed at FNC, the uncertainty of aerosol concentration evaluated by Gaussian error propagation law is less than 1%. The results of uncertainty estimation in the aerosol sampling system will be utilized for the system performance data.

Speciation of organotin compounds in environmental samples by GC-ICPMS

International Nuclear Information System (INIS)

Vahcic, M.; Milacic, R.; Scancar, J.

2009-01-01

Full text: Analytical procedure using 15 m GC column was applied for simultaneous speciation of OTCs in various environmental samples. Methyl-, butyl-, phenyl- and octyl- tin species were quantitatively determined. different extraction reagents and conditions were studied. OTCs species were derivatized by NaBEt 4 and extracted into isooctane or hexane. The applied analytical procedure considerably shortened analytical time and enabled simultaneous determination of 12 OTCs in environmental samples. (author)

Establishing adequate conditions for mercury determination in environmental samples by INAA

International Nuclear Information System (INIS)

Perez, Caroline; Santos, Eliane C.; Saiki, Mitiko

2017-01-01

Mercury (Hg) is a toxic element released into the environment mainly by anthropic activities. Consequently, the improvement for Hg determination in environmental samples is of great interest. Instrumental Neutron Activation Analysis (INAA) is considered an adequate method to determine several elements. However, Hg determination by INAA is often hampered by its volatility, which causes losses. The aim of this study was to establish adequate irradiation conditions for Hg determination in environmental samples by INAA. The following parameters were evaluated: irradiation time, container for irradiation and spectral gamma ray interferences. For the study, aliquots of certified reference materials (CRMs) and tree bark samples were irradiated together with Hg synthetic standard at the IEA-R1 nuclear research reactor. Gamma ray activities of 1 97 Hg and 203 Hg were measured in a spectrometer coupled to a HGe detector. Results obtained indicated that polyethylene capsules or envelopes can be used as container for sample irradiation and the Hg impurities in these containers were negligible. Irradiation time of one hour was adequate for Hg determination and in long irradiations of 8 h problems of spectral interference of 198 Au and 75 Se were observed. In addition, Hg loss during the irradiation of 1 h and after irradiation was not observed. Quality control of Hg results, obtained in the CRMs analyses using one hour of irradiation, indicated good precision and accuracy with |Z score| < 2. The experimental conditions established in this study were applied to tree bark samples. Detection limits for Hg of these analyses were between 0.14 and 1.9 μg g -1 . (author)

Environmental sample banking-research and methodology

International Nuclear Information System (INIS)

Becker, D.A.

1976-01-01

The National Bureau of Standards (NBS), in cooperation with the Environment Protection Agency and the National Science Foundation, is engaged in a research program establishing methodology for environmental sample banking. This program is aimed toward evaluating the feasibility of a National Environment Specimen Bank (NESB). The capability for retrospective chemical analyses to evaluate changes in our environment would provide useful information. Much of this information could not be obtained using data from previously analyzed samples. However, to assure validity for these stored samples, they must be sampled, processed and stored under rigorously evaluated, controlled and documented conditions. The program currently under way in the NBS Analytical Chemistry Division has 3 main components. The first is an extension survey of available literature concerning problems of contamination, losses and storage. The components of interest include trace elements, pesticides, other trace organics (PCBs, plasticizers, etc.), radionuclides and microbiological species. The second component is an experimental evaluation of contamination and losses during sampling and sample handling. Of particular interest here is research into container cleaning methodology for trace elements, with respect to adsorption, desorption, leaching and partial dissolution by various sample matrices. The third component of this program is an evaluation of existing methodology for long-term sample storage

Environmental Measurements Laboratory. Environmental report, September 1, 1981-March 1, 1982

International Nuclear Information System (INIS)

Hardy, E.P. Jr.; Toonkel, L.E.

1982-01-01

This report presents current information from the EML environmental programs, the Radiological and Environmental Research Division at Argonne National Laboratory and the Los Alamos National Laboratory. Two reports on radionuclide data quality assurance are presented in the initial section: one dealing with fallout and biological samples and the other with filtered air samples. These are followed by a report on stratospheric tritium injection by the October 1980 Chinese test. The second section presents recent data from EML progams strontium-90 fallout, radionuclides and trace metals in surface air, radioactivity and trace gases sampled in the stratosphere by aircraft and balloons, strontium-90 in San Francisco and New York diet, milk, and tap water, and cesium-137 in tap water. The third section presents data from Argonne National Laboratory on cesium-137 in Chicago food and from Los Alamos National Laboratory on tritium in the stratosphere. A bibliography of recent publications related to environmental studies is presented. Each section has been abstracted and indexed individually for ERA/EDB

Environmental Measurements Laboratory annual report, calendar year 1980

International Nuclear Information System (INIS)

Volchok, H.L.

1981-05-01

The 1980 Annual Report is presented as a series of abstracts, organized by broad programmatic headings under the five technical Laboratory Divisions and one Branch. In addition, a short section appears at the end of the report describing the organization, staff, outside activities and our publications and presentations for the year. Research performaed by the Environmental Studies Division is reported under the following categories: high altitude sampling program, deposition and surface air, and the biosphere. Measurement methods research and air quality field studies are reported by the Aerosol Studies Division. The Radiation Physics Division reported research on radiation transport theory, radiation dosimetry, environmental radioactivity, and the assessment of non-nuclear energy technologies. Research in the Analytical Chemistry Division is reported on quality assurance, analytical support of research projects, analytical development for research projects, and programmatic research. The Instrumentation Division reported research on the development of instrumentation in various categories. The Applied Mathematics Branch reported results of programs for aerosol studies, analytical chemistry, environmental studies, and radiation physics

Gamma-spectrometry of extended sources for analysing environmental samples

International Nuclear Information System (INIS)

Jarosievitz, B.

1996-01-01

Measurements of the environmental activity concentration by gamma spectrometers require the determination of the full-energy-peak efficiency as a function of photon energy over the detector range. This can be done by experiments or by calculation. For simple cases, experiments are straightforward, but if the decay scheme is complex, cascade effects modify detection efficiency. Also, actual detection efficiency depends on the detection geometry. All these effects are treated as corrections or modifications of the simple value cases which are especially relevant when applied to large volume of environmental samples. In this thesis calculations are made, using the GEANT MC program, for realistic experimental situations that have been performed, and these calculations are validated. The calculational and experimental results have been compared, and if it proves to be satisfactory, the results can be relied on even for cases when no direct experimental observation is possible. The general problems of gamma spectroscopy and correction problems are discussed. The two main tools, the experimental setup and the simulation program are described. A careful checking of the simulation results and the consequences are presented. (R.P.)

Use of plasma-source multicollector magnetic-sector mass spectrometry for uranium and plutonium analysis in environmental samples

International Nuclear Information System (INIS)

Price Russ, G.; Williams, Ross

2001-01-01

Full text: The ability to detect and isotopically characterize uranium and plutonium in environmental samples is of primary importance in the search for nuclear proliferation. The utility of isotope ratio measurements for environmental monitoring is limited by sample preparation costs, measurement precision, and sensitivity. This is particularly true for wide-area monitoring where the number of samples required varies inversely with obtainable precision and sensitivity. Historically isotopic measurements have been made by thermal ionization mass spectrometry (TIMS). While requiring extensive sample preparation, no other technique matched its precision and sensitivity for such measurements. Inductively-coupled-plasma, magnetic-sector, multicollector, mass spectrometry offers the prospect of extending the state-of-the-art to higher precision while increasing sensitivity and reducing costs through more rapid analysis and reduced sample preparation. At LLNL this technique is being implemented in the form of an IsoProbe (Micromass, UK). This paper will present data for both standards and IAEA supplied samples demonstrating the power and limitations of the technique. The precision and sensitivity of the IsoProbe results will be compared to TIMS performance for comparable samples. For 48 determinations of natural uranium, using the double spike to correct for bias, a relative standard deviation of 0.04% (1σ) for 238 U/ 235 U has been obtained in a preliminary study. This is a substantial improvement over the TIMS result of 0.1% reported at the previous conference. Further improvements can be expected as we gain a better understanding of the background peaks occurring in the IsoProbe spectra. (author)

The importance of sound methodology in environmental DNA sampling

Science.gov (United States)

T. M. Wilcox; K. J. Carim; M. K. Young; K. S. McKelvey; T. W. Franklin; M. K. Schwartz

2018-01-01

Environmental DNA (eDNA) sampling - which enables inferences of species’ presence from genetic material in the environment - is a powerful tool for sampling rare fishes. Numerous studies have demonstrated that eDNA sampling generally provides greater probabilities of detection than traditional techniques (e.g., Thomsen et al. 2012; McKelvey et al. 2016; Valentini et al...

Measurement of technetium-99 in soil samples collected in Marshall Islands

Energy Technology Data Exchange (ETDEWEB)

Tagami, K.; Uchida, S. [National Inst. of Radiological Sciences, Environmental and Toxicological Sciences Research Group, Chiba (Japan)

2000-07-01

Extraction techniques for recovery of technetium-99 ({sup 99}Tc) for ICP-MS measurements were evaluated using soil samples collected from the Marshall Islands. The results of three different extraction techniques were compared: (M1) acid leaching of Tc from ashed soil; (M2) acid leaching of Tc from raw dry soil; and (M3) Tc volatilization from ashed soil using a combustion apparatus. Total Tc recoveries varied considerably between the extraction techniques but each method yielded similar analytical results for {sup 99}Tc. Applications of these extraction techniques to a series of environmental samples and ICP-MS measurements have yielded first data on the {sup 99}Tc content of Marshall Islands soil samples contaminated with close-in radioactive fallout from nuclear weapons testing. The {sup 99}Tc activity concentration in the soil samples ranged between 0.1 and 1.1 mBq/g-dw. The limit of detection for {sup 99}Tc by ICP-MS was 0.17 mBq per sample or 0.014 mBq/g-dw under standard operating conditions. (author)

Measurement of technetium-99 in soil samples collected in Marshall Islands

International Nuclear Information System (INIS)

Tagami, K.; Uchida, S.

2000-01-01

Extraction techniques for recovery of technetium-99 ( 99 Tc) for ICP-MS measurements were evaluated using soil samples collected from the Marshall Islands. The results of three different extraction techniques were compared: (M1) acid leaching of Tc from ashed soil; (M2) acid leaching of Tc from raw dry soil; and (M3) Tc volatilization from ashed soil using a combustion apparatus. Total Tc recoveries varied considerably between the extraction techniques but each method yielded similar analytical results for 99 Tc. Applications of these extraction techniques to a series of environmental samples and ICP-MS measurements have yielded first data on the 99 Tc content of Marshall Islands soil samples contaminated with close-in radioactive fallout from nuclear weapons testing. The 99 Tc activity concentration in the soil samples ranged between 0.1 and 1.1 mBq/g-dw. The limit of detection for 99 Tc by ICP-MS was 0.17 mBq per sample or 0.014 mBq/g-dw under standard operating conditions. (author)

A new measurement method for quantification and speciation of technetium-99 in sample at environmental concentrations

Energy Technology Data Exchange (ETDEWEB)

Kasprzak, L.M. [IRSN/DEI/STEME/LMRE, ORSAY, F-91400 (France); SUBATECH, EMN-IN2P3/CNRS-Universit Nantes, F-44307 (France); Aubert, C.; Cossonnet, C. [IRSN/DEI/STEME/LMRE, ORSAY, F-91400 (France); Fattahi, M. [SUBATECH, EMN-IN2P3/CNRS-Universit Nantes, F-44307 (France)

2006-07-01

Technetium-99 is a pure {beta}- emitter and important long half-lived multi-valent radionuclide to be considered in radiation protection of the environment and the public. It a fission product of both {sup 235}U and {sup 239}Pu with approximately a 6% yield. The most stable and very mobile form of Tc is the pertechnetate anion (TcO{sub 4}{sup -}). Therefore, environmental monitoring requires the knowledge of the redox and chemical properties of this element in order to predict its behaviour and transfer in the environment. Given the extremely low concentration of {sup 99}Tc in the environment (10{sup -10} M to 10{sup -12} M), its determination currently necessitates an enrichment and separation from the sample matrix prior to instrumental measurement. To this end, the development of a suitable analytical technique is required. The advantages of Capillary Electrophoresis (CE) as a powerful separation technique can be combined with the atomic specificity, multi-elemental character and extremely high sensitivity of an inductively coupled plasma mass spectrometer (ICP-MS) for trace metal-speciation studies in different fields of interest. However, the coupling of both commercially available instruments deserves particular attention if separative resolution, high analyte transport efficiency and sensitive detection are to be achieved. In, that technical vein, the interface itself may be considered as the 'key to success'. Several attempts to develop interfaces for CE-ICP-MS have been described over the last few years. However, the {sup 99}Tc quantification by ICP-MS can be disturbed by isobaric overlaps {sup 99}Ru and interferences induced by the matrix, including those associated with hydride formation ({sup 98}Mo{sup 1}H (23.8%), {sup 98}Ru{sup 1}H (1.9%)). The aim of the present study was to develop a rapid and efficient method for the determination of {sup 99}Tc in environmental samples by CE-ICP-MS without preliminary classical radiochemical separation to

Hanford Site Environmental Surveillance Master Sampling Schedule for Calendar Year 2010

Energy Technology Data Exchange (ETDEWEB)

Bisping, Lynn E.

2010-01-08

Environmental surveillance of the Hanford Site and surrounding areas is conducted by Pacific Northwest National Laboratory for the U.S. Department of Energy (DOE). Sampling is conducted to evaluate levels of radioactive and nonradioactive pollutants in the Hanford Site environs per regulatory requirements. This document contains the calendar year 2010 schedule for the routine collection of samples for the Surface Environmental Surveillance Project and the Drinking Water Monitoring Project. Each section includes sampling locations, sampling frequencies, sample types, and analyses to be performed. In some cases, samples are scheduled on a rotating basis. If a sample will not be collected in 2010, the anticipated year for collection is provided. Maps showing approximate sampling locations are included for media scheduled for collection in 2010.

Wet-digestion of environmental sample using silver-mediated electrochemical method

International Nuclear Information System (INIS)

Kuwabara, Jun

2010-01-01

An application of silver-mediated electrochemical method to environmental samples as the effective digestion method for iodine analysis was tried. Usual digestion method for 129 I in many type of environmental sample is combustion method using quartz glass tube. Chemical yield of iodine on the combustion method reduce depending on the type of sample. The silver-mediated electrochemical method is expected to achieve very low loss of iodine. In this study, dried kombu (Laminaria) sample was tried to digest with electrochemical cell. At the case of 1g of sample, digestion was completed for about 24 hours under the electric condition of <10V and <2A. After the digestion, oxidized species of iodine was reduced to iodide by adding sodium sulfite. And then the precipitate of silver iodide was obtained. (author)

Determination of [sup 90]Sr in environmental samples with resonance ionization spectroscopy in collinear geometry

Energy Technology Data Exchange (ETDEWEB)

Zimmer, K. (Inst. fuer Physik, Univ. Mainz (Germany)); Stenner, J. (Inst. fuer Physik, Univ. Mainz (Germany)); Kluge, H.J. (Inst. fuer Physik, Univ. Mainz (Germany)); Lantzsch, J. (Inst. fuer Physik, Univ. Mainz (Germany)); Monz, L. (Inst. fuer Physik, Univ. Mainz (Germany)); Otten, E.W. (Inst. fuer Physik, Univ. Mainz (Germany)); Passler, G. (Inst. fuer Physik, Univ. Mainz (Germany)); Schwalbach, R. (Inst. fuer Physik, Univ. Mainz (Germany)); Schwarz, M. (Inst. fuer Physik, Univ. Mainz (Germany)); Stevens, H. (Inst. fuer Physik, Univ. Mainz (Germany)); Wendt, K. (Inst. fuer Physik, Univ. Mainz (Germany)); Herrmann, G. (Inst. fuer Kernchemie, Univ. Mainz (Germany)); Niess, S. (Inst. fuer Kernchemie, Univ. Mainz (Germany)); Trautmann, N. (Inst. fuer Kernchemie, Univ. Mainz (Germany)); Walter, K. (Inst. fuer Kernchemie, Univ. Mainz (Germany)); Bushaw, B.A. (Pacific Northwest Lab., Richland, WA (United States))

1994-08-01

A new, fast technique for trace analysis of the radioactive isotopes [sup 89]Sr and [sup 90]Sr in environmental samples has been developed. Conventional mass separation is combined with resonance ionization spectroscopy in collinear geometry, which provides high selectivity and sensitivity. In addition, a chemical separation procedure for sample preparation has been developed. The described technique was used to determine the [sup 90]Sr content in [approx] 870 m[sup 3] air samples collected near Munich during and shortly after the Chernobyl reactor accident in April 1986. The content of [sup 90]Sr was measured to be 1.4 mBq per m[sup 3], corresponding to 1.6 x 10[sup 9] atoms of [sup 90]Sr per sample. This value is in good agreement with the results of radiochemical measurements. (orig.)

Current status of JAERI program on development of ultra-trace-analytical technology for safeguards environmental samples

International Nuclear Information System (INIS)

Adachi, T.; Usuda, S.; Watanabe, K.

2001-01-01

Full text: In order to contribute to the strengthened safeguards system based on the Program 93+2 of the IAEA, Japan Atomic Energy Research Institute (JAERI) is developing analytical technology for ultra-trace amounts of nuclear materials in environmental samples, and constructed the CLEAR facility (Clean Laboratory for Environmental Analysis and Research) for this purpose. The development of the technology is carried out, at existing laboratories for time being, in the following fields: screening, bulk analysis and particle analysis. The screening aims at estimating the amounts of nuclear materials in environmental samples to be introduced into the clean rooms, and is the first step to avoid cross-contamination among the samples and contamination of the clean rooms themselves. In addition to ordinary radiation spectrometry, Compton suppression technique was applied to low energy γ- and X-ray measurements, and sufficient reduction in background level has been demonstrated. Another technique in examination is imaging-plate method, which is a kind of autoradiography and suitable for determination of radioactive-particle distribution in the samples as well as for semiquantitative determination. As for the bulk analysis, the efforts are temporally made on uranium in swipe samples. Preliminary examination for optimization of sample pre-treatment conditions is in progress. At present, ashing by low-temperature-plasma method gives better results than high-temperature ashing or acid leaching. For the isotopic ratio measurement, instrumental performance of inductively-coupled plasma mass spectrometry (ICP-MS) are mainly examined because sample preparation for ICP-MS is simpler than that for thermal ionization mass spectrometry (TIMS). It was found by our measurement that the swipe material (TexWipe TX304, usually used by IAEA) contains un-negligible uranium blank with large deviation (2-6 ng/sheet). This would introduce significant uncertainty in the trace analysis. JAERI

A comparison between the measurements of Kr-85 in environmental samples by liquid scintillation and proportional counters

International Nuclear Information System (INIS)

Heras Iniquez, M.C.; Perez Garcia, M.M.

1983-01-01

The most used methods for the measurement of Kr-81 beta-activity after their concentration and aisolation are the liquid scintillation counting and the proportional counter. In this work the beta activity of concentrated and aisolated Kr-85 samples measured in collaboration with the Max-Planck Institut fur Kernphyslk, Aussenstelle Freiburg. Samples taken both In Madrid and Frelburg are measured by proportional counters in the Max-Planck lnstitut, Freibury and by liquid scintillation counting in JEN, Madrid. The comparison of both measurements do not show appreciable discrepancy between the results obtained to both techniques. (Author)

Fluoroquinolone antibiotics in environmental waters: sample preparation and determination.

Science.gov (United States)

Speltini, Andrea; Sturini, Michela; Maraschi, Federica; Profumo, Antonella

2010-04-01

The aim of this review is to provide a general overview on the analytical methods proposed in the last decade for trace fluoroquinolone (FQ) determination in environmental waters. A large number of studies have been developed on this topic in reason of the importance of their monitoring in the studies of environmental mobility and potential degradation pathways. Every step of the analysis has been carefully considered, with a particular attention to sample preparation, in relationship with the problems involved in the analysis of real matrices. The different strategies to minimise interference from organic matter and to achieve optimal sensitivity, especially important in those samples with lower FQ concentrations, were also highlighted. Results and progress in this field have been described and critically commented. Moreover, a worldwide overview on the presence of FQs in the environmental waters has been reported.

ENVIRONMENTAL SAMPLING USING LOCATION SPECIFIC AIR MONITORING IN BULK HANDLING FACILITIES

Energy Technology Data Exchange (ETDEWEB)

Sexton, L.; Hanks, D.; Degange, J.; Brant, H.; Hall, G.; Cable-Dunlap, P.; Anderson, B.

2011-06-07

Since the introduction of safeguards strengthening measures approved by the International Atomic Energy Agency (IAEA) Board of Governors (1992-1997), international nuclear safeguards inspectors have been able to utilize environmental sampling (ES) (e.g. deposited particulates, air, water, vegetation, sediments, soil and biota) in their safeguarding approaches at bulk uranium/plutonium handling facilities. Enhancements of environmental sampling techniques used by the IAEA in drawing conclusions concerning the absence of undeclared nuclear materials or activities will soon be able to take advantage of a recent step change improvement in the gathering and analysis of air samples at these facilities. Location specific air monitoring feasibility tests have been performed with excellent results in determining attribute and isotopic composition of chemical elements present in an actual test-bed sample. Isotopic analysis of collected particles from an Aerosol Contaminant Extractor (ACE) collection, was performed with the standard bulk sampling protocol used throughout the IAEA network of analytical laboratories (NWAL). The results yielded bulk isotopic values expected for the operations. Advanced designs of air monitoring instruments such as the ACE may be used in gas centrifuge enrichment plants (GCEP) to detect the production of highly enriched uranium (HEU) or enrichments not declared by a State. Researchers at Savannah River National Laboratory in collaboration with Oak Ridge National Laboratory are developing the next generation of ES equipment for air grab and constant samples that could become an important addition to the international nuclear safeguards inspector's toolkit. Location specific air monitoring to be used to establish a baseline environmental signature of a particular facility employed for comparison of consistencies in declared operations will be described in this paper. Implementation of air monitoring will be contrasted against the use of smear

An environmental sample chamber for reliable scanning transmission x-ray microscopy measurements under water vapor

Energy Technology Data Exchange (ETDEWEB)

Kelly, Stephen T.; Nigge, Pascal; Prakash, Shruti; Gilles, Mary K. [Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720 (United States); Laskin, Alexander; Wang, Bingbing [William R. Wiley Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352 (United States); Tyliszczak, Tolek [Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, California 94720 (United States); Leone, Stephen R. [Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720 (United States); Department of Chemistry and Department of Physics, University of California, Berkeley, California 94720 (United States)

2013-07-15

We have designed, fabricated, and tested a compact gas-phase reactor for performing in situ soft x-ray scanning transmission x-ray microscopy (STXM) measurements. The reactor mounts directly to the existing sample holder used in the majority of STXM instruments around the world and installs with minimal instrument reconfiguration. The reactor accommodates many gas atmospheres, but was designed specifically to address the needs of measurements under water vapor. An on-board sensor measures the relative humidity and temperature inside the reactor, minimizing uncertainties associated with measuring these quantities outside the instrument. The reactor reduces x-ray absorption from the process gas by over 85% compared to analogous experiments with the entire STXM instrument filled with process gas. Reduced absorption by the process gas allows data collection at full instrumental resolution, minimizes radiation dose to the sample, and results in much more stable imaging conditions. The reactor is in use at the STXM instruments at beamlines 11.0.2 and 5.3.2.2 at the Advanced Light Source.

Standardizing measurement, sampling and reporting for public exposure assessments

Energy Technology Data Exchange (ETDEWEB)

Rochedo, Elaine R.R. [Instituto de Radioprotecao e Dosimetria, Comissao Nacional de Energia Nuclear, Av. Salvador Allende s/No. CEP 22780-160 Rio de Janeiro, RJ (Brazil)], E-mail: elaine@ird.gov.br

2008-11-15

UNSCEAR assesses worldwide public exposure from natural and man-made sources of ionizing radiation based on information submitted to UNSCEAR by United Nations Member States and from peer reviewed scientific literature. These assessments are used as a basis for radiation protection programs of international and national regulatory and research organizations. Although UNSCEAR describes its assessment methodologies, the data are based on various monitoring approaches. In order to reduce uncertainties and improve confidence in public exposure assessments, it would be necessary to harmonize the methodologies used for sampling, measuring and reporting of environmental results.

Hanford Site Environmental Surveillance Master Sampling Schedule for Calendar Year 2009

Energy Technology Data Exchange (ETDEWEB)

Bisping, Lynn E.

2009-01-20

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest National Laboratory for the U.S. Department of Energy. Sampling is conducted to evaluate levels of radioactive and nonradioactive pollutants in the Hanford environs, as required in DOE Order 450.1 and DOE Order 5400.5. This document contains the calendar year 2009 schedule for the routine collection of samples for the Surface Environmental Surveillance Project and Drinking Water Monitoring Project. Each section includes sampling locations, sampling frequencies, sample types, and analyses to be performed. In some cases, samples are scheduled on a rotating basis. If a sample will not be collected in 2009, the anticipated year for collection is provided. Maps showing approximate sampling locations are included for media scheduled for collection in 2009.

Neutron-induced prompt gamma-ray analysis of Gulf marine environmental samples

International Nuclear Information System (INIS)

Yonezawa, C.; Matsue, H.; Adachi, T.; Hoshi, M.; Tachikawa, E.; Povinec, P.P.; Fowler, S.W.; Baxter, M.S.

1999-01-01

Multi-element composition and isotopic characteristics of the oil and contaminated materials, and measurement of historical records of marine environmental condition using annual bands in coral samples have been investigated in the program. Elemental analyses have been carried out by the PGA together with INAA and ICP-MS to obtain accurate and precise elemental characteristics of oil, marine sediment and bivalves. Fifteen elements including light elements of H, B, N, Si and Ca which cannot be determined by INAA and ICP-MS, were determined by the PGA. Altogether 43 elements were determined

Sequim Marine Research Laboratory routine environmental measurements during CY-1978

International Nuclear Information System (INIS)

Houston, J.R.; Blumer, P.J.

1979-03-01

Environmental data collected during 1978 in the vicinity of the Marine Research Laboratory show continued compliance with all applicable state and federal regulations and furthermore show no detectable change from conditions that existed in previous years. Samples collected for radiological analysis included soil, drinking water, bay water, clams, and seaweed. Radiation dose rates at 1 meter aboveground were also measured

Solid-phase extraction and determination of trace elements in environmental samples using naphthalene adsorbent

International Nuclear Information System (INIS)

Pourreza, N.

2004-01-01

Naphthalene co-precipitated with quaternary ammonium salt such as tetraoctyl ammonium bromide and methyltrioctyl ammonium chloride have been used as adsorbent for solid phase extraction of metal ions such as Hg, Cd and Fe. The metal ions are retained on the adsorbent in a column as their complexes with suitable ligands and eluted by an eluent before instrumental measurements. The optimization of the procedures for solid phase extraction and consequent determination of trace elements and application to environmental samples especially water samples will be discussed. (author)

Joint sampling programme-Verification of data obtained in environmental monitoring

Energy Technology Data Exchange (ETDEWEB)

Lauria, D.C. [Instituto de Radioprotecao e Dosimetria, Comissao Nacional de Energia Nuclear, Av. Salvador Allende s/no., CEP 22780-160, Rio de Janeiro, RJ (Brazil)], E-mail: dejanira@ird.gov.br; Martins, N.S.F.; Vasconcellos, M.L.H.; Zenaro, R.; Peres, S.S.; Pires do Rio, M.A. [Instituto de Radioprotecao e Dosimetria, Comissao Nacional de Energia Nuclear, Av. Salvador Allende s/no., CEP 22780-160, Rio de Janeiro, RJ (Brazil)

2008-11-15

The objective of the Environmental Radiological Monitoring Control programme carried out by the Institute of Radiation Protection and Dosimetry (IRD) in Brazil is to verify the licensee's compliance with the requirements for environmental monitoring of Brazilian facilities. The Joint Sampling Programme (JSP) is just one part of the control programme. In order to verify that the data reported by the licensees is representative and legitimate, this programme verifies sampling procedures, accuracy and precision of the data and the changes in the environmental conditions. This paper discusses the main findings of this programme that allowed IRD to optimize its available resources to control the monitoring of the eight facilities in Brazil.

Establishing adequate conditions for mercury determination in environmental samples by INAA

Energy Technology Data Exchange (ETDEWEB)

Perez, Caroline; Santos, Eliane C.; Saiki, Mitiko, E-mail: caroline.perez@usp.br [Instituto de Pesquisas Energéticas e Nucleares (IPEN/CNEN-SP), São Paulo, SP (Brazil)

2017-07-01

Mercury (Hg) is a toxic element released into the environment mainly by anthropic activities. Consequently, the improvement for Hg determination in environmental samples is of great interest. Instrumental Neutron Activation Analysis (INAA) is considered an adequate method to determine several elements. However, Hg determination by INAA is often hampered by its volatility, which causes losses. The aim of this study was to establish adequate irradiation conditions for Hg determination in environmental samples by INAA. The following parameters were evaluated: irradiation time, container for irradiation and spectral gamma ray interferences. For the study, aliquots of certified reference materials (CRMs) and tree bark samples were irradiated together with Hg synthetic standard at the IEA-R1 nuclear research reactor. Gamma ray activities of 1{sup 97}Hg and {sup 203}Hg were measured in a spectrometer coupled to a HGe detector. Results obtained indicated that polyethylene capsules or envelopes can be used as container for sample irradiation and the Hg impurities in these containers were negligible. Irradiation time of one hour was adequate for Hg determination and in long irradiations of 8 h problems of spectral interference of {sup 198}Au and {sup 75}Se were observed. In addition, Hg loss during the irradiation of 1 h and after irradiation was not observed. Quality control of Hg results, obtained in the CRMs analyses using one hour of irradiation, indicated good precision and accuracy with |Z score| < 2. The experimental conditions established in this study were applied to tree bark samples. Detection limits for Hg of these analyses were between 0.14 and 1.9 μg g{sup -1}. (author)

Rapid and Automated Determination of Plutonium and Neptunium in Environmental Samples

DEFF Research Database (Denmark)

Qiao, Jixin

This thesis presents improved analytical methods for rapid and automated determination of plutonium and neptunium in environmental samples using sequential injection (SI) based chromatography and inductively coupled plasma mass spectrometry (ICP-MS). The progress of methodology development...... and optimization for rapid determination of plutonium in environmental samples using SIextraction chromatography prior to inductively coupled plasma mass spectrometry (Paper III); (3) Development of an SI-chromatographic method for simultaneous determination of plutonium and neptunium in environmental samples...... for rapid and simultaneous determination of plutonium and neptunium within an SI system (Paper VI). The results demonstrate that the developed methods in this study are reliable and efficient for accurate assays of trace levels of plutonium and neptunium as demanded in different situations including...

The use of EURACHEM guide for comparison of two 210Pb determination methods in solid environmental samples

International Nuclear Information System (INIS)

Al-Masri, M. S.; Hassan, M.; Amin, Y.

2008-07-01

Two techniques for determination of 210 Pb in solid environmental samples have been validated and compared according to Eurachem Guide on method validation. The first technique depended on determination of 210 Po, which equilibrium with 210 Pb, by platting it onto a rotating silver disc. Then, Alpha counting of 210 Po was done using an alpha spectrometer. On the other hand, according to its decay scheme, 210 Pb was measured directly through gamma spectrometry by measuring the 46.5 keV. Detection limits, reproducibility and recovery coefficient were the main validation parameters. In addition, uncertainties of measurement were estimated and compared for the two techniques. The comparison results have shown that, the activity of 210 Pb in the environmental samples can choose which technique is appropriated. It was found that Eurachem Guide and comparison of quality statistical validation parameters can be a good tool for selection of the appropriate method for the application. (Authors)

Infrared characterization of environmental samples by pulsed photothermal spectroscopy

International Nuclear Information System (INIS)

Seidel, W.; Foerstendorf, H.; Heise, K.H.; Nicolai, R.; Schamlott, A.; Ortega, J.M.; Glotin, F.; Prazeres, R.

2004-01-01

Low concentration of toxic radioactive metals in environmental samples often limits the interpretation of results of infrared studies investigating the interaction processes between the metal ions and environmental compartments. For the first time, we could show that photothermal infrared spectroscopy performed with a pulsed free electron laser can provide reliable infrared spectra throughout a distinct spectral range of interest. In this model investigation, we provide vibrational absorption spectra of a rare earth metal salt dissolved in a KBr matrix and a natural calcite sample obtained by photothermal beam deflection (PTBD) technique and FT-IR (Fourier-transform infrared) spectroscopy, respectively. General agreement was found between all spectra of the different recording techniques. Spectral deviations were observed with samples containing low concentration of the rare earth metal salt indicating a lower detection limit of the photothermal method as compared to conventional FT-IR spectroscopy. (authors)

Qualitative and quantitative analysis of environmental samples by laser-induced breakdown spectrometry

International Nuclear Information System (INIS)

Zorov, N B; Popov, A M; Zaytsev, S M; Labutin, T A

2015-01-01

The key achievements in the determination of trace amounts of components in environmental samples (soils, ores, natural waters, etc.) by laser-induced breakdown spectrometry are considered. Unique capabilities of this method make it suitable for rapid analysis of metals and alloys, glasses, polymers, objects of cultural heritage, archaeological and various environmental samples. The key advantages of the method that account for its high efficiency are demonstrated, in particular, a small amount of analyzed material, the absence of sample preparation, the possibility of local and remote analysis of either one or several elements. The use of chemometrics in laser-induced breakdown spectrometry for qualitative sample classification is described in detail. Various approaches to improving the figures of merit of quantitative analysis of environmental samples are discussed. The achieved limits of detection for most elements in geochemical samples are critically evaluated. The bibliography includes 302 references

Rapid and automated determination of plutonium and neptunium in environmental samples

International Nuclear Information System (INIS)

Qiao, J.

2011-03-01

This thesis presents improved analytical methods for rapid and automated determination of plutonium and neptunium in environmental samples using sequential injection (SI) based chromatography and inductively coupled plasma mass spectrometry (ICP-MS). The progress of methodology development in this work consists of 5 subjects stated as follows: 1) Development and optimization of an SI-anion exchange chromatographic method for rapid determination of plutonium in environmental samples in combination of inductively coupled plasma mass spectrometry detection (Paper II); (2) Methodology development and optimization for rapid determination of plutonium in environmental samples using SI-extraction chromatography prior to inductively coupled plasma mass spectrometry (Paper III); (3) Development of an SI-chromatographic method for simultaneous determination of plutonium and neptunium in environmental samples (Paper IV); (4) Investigation of the suitability and applicability of 242 Pu as a tracer for rapid neptunium determination using anion exchange chromatography in an SI-network coupled with inductively coupled plasma mass spectrometry (Paper V); (5) Exploration of macro-porous anion exchange chromatography for rapid and simultaneous determination of plutonium and neptunium within an SI system (Paper VI). The results demonstrate that the developed methods in this study are reliable and efficient for accurate assays of trace levels of plutonium and neptunium as demanded in different situations including environmental risk monitoring and assessment, emergency preparedness and surveillance of contaminated areas. (Author)

Rapid and automated determination of plutonium and neptunium in environmental samples

Energy Technology Data Exchange (ETDEWEB)

Qiao, J.

2011-03-15

This thesis presents improved analytical methods for rapid and automated determination of plutonium and neptunium in environmental samples using sequential injection (SI) based chromatography and inductively coupled plasma mass spectrometry (ICP-MS). The progress of methodology development in this work consists of 5 subjects stated as follows: 1) Development and optimization of an SI-anion exchange chromatographic method for rapid determination of plutonium in environmental samples in combination of inductively coupled plasma mass spectrometry detection (Paper II); (2) Methodology development and optimization for rapid determination of plutonium in environmental samples using SI-extraction chromatography prior to inductively coupled plasma mass spectrometry (Paper III); (3) Development of an SI-chromatographic method for simultaneous determination of plutonium and neptunium in environmental samples (Paper IV); (4) Investigation of the suitability and applicability of 242Pu as a tracer for rapid neptunium determination using anion exchange chromatography in an SI-network coupled with inductively coupled plasma mass spectrometry (Paper V); (5) Exploration of macro-porous anion exchange chromatography for rapid and simultaneous determination of plutonium and neptunium within an SI system (Paper VI). The results demonstrate that the developed methods in this study are reliable and efficient for accurate assays of trace levels of plutonium and neptunium as demanded in different situations including environmental risk monitoring and assessment, emergency preparedness and surveillance of contaminated areas. (Author)

Analysis procedure for americium in environmental samples

International Nuclear Information System (INIS)

Holloway, R.W.; Hayes, D.W.

1982-01-01

Several methods for the analysis of 241 Am in environmental samples were evaluated and a preferred method was selected. This method was modified and used to determine the 241 Am content in sediments, biota, and water. The advantages and limitations of the method are discussed. The method is also suitable for 244 Cm analysis

Application of semiempirical expressions to the alpha and beta radiometry of environmental depositions samples

International Nuclear Information System (INIS)

Perez Tamayo, L.

1996-01-01

Were applied two semiempirical equations exponential beta absorption and Bragg-Kleeman approximation complementary to experimental corrections for beta backscattering and auto absorption of beta and alpha radiations in measurements of environmental depositions samples In the first case was verified the validity of mentioned corrections with an application boundary to mass greater than 300 Pb-210 (0.015 mg/cm 2 ) In the second case, the Bragg-Kleeman approximation combined with the experimental beta corrections, bring a judgment to determine the fundamental alpha and beta emisors samples which results the Pb-210 group

Sampling methods for recovery of human enteric viruses from environmental surfaces.

Science.gov (United States)

Turnage, Nicole L; Gibson, Kristen E

2017-10-01

Acute gastroenteritis causes the second highest infectious disease burden worldwide. Human enteric viruses have been identified as leading causative agents of acute gastroenteritis as well as foodborne illnesses in the U.S. and are generally transmitted by fecal-oral contamination. There is growing evidence of transmission occurring via contaminated fomite including food contact surfaces. Additionally, human enteric viruses have been shown to remain infectious on fomites over prolonged periods of time. To better understand viral persistence, there is a need for more studies to investigate this phenomenon. Therefore, optimization of surface sampling methods is essential to aid in understanding environmental contamination to ensure proper preventative measures are being applied. In general, surface sampling studies are limited and highly variable among recovery efficiencies and research parameters used (e.g., virus type/density, surface type, elution buffers, tools). This review aims to discuss the various factors impacting surface sampling of viruses from fomites and to explore how researchers could move towards a more sensitive and standard sampling method. Copyright © 2017 Elsevier B.V. All rights reserved.

Radiological analyses of Marshall Islands environmental samples, 1974--1976

International Nuclear Information System (INIS)

Greenhouse, N.A.; Miltenberger, R.P.; Cua, F.T.

1977-01-01

Results are reported from the radiological analysis of environmental samples collected in the Marshall Islands during 1974 through 1976. Most of the samples were collected on or near the Bikini Atoll and included plants, soil, fish, catchment water, and sediments, with emphasis on local marine and terrestrial food items. Data are presented from γ spectral analysis and the content of 90 Sr and transuranic elements in the samples

Quality assurance of external exposure measurement for national survey of environmental natural radioactive level

International Nuclear Information System (INIS)

Yue Qingyu

1995-01-01

This paper summarizes the quality assurance work of external exposure measurement for national survey of environmental natural radioactive level. It mainly introduces instrumentation used in external exposure measurement and its properties, the measurement results of three times of national in-site intercomparison, and in-site sample check results of measurement results from 29 provinces, cities and autonomous regions and Wuhan, Baotou cities

Radiochemistry methods in DOE Methods for Evaluating Environmental and Waste Management Samples: Addressing new challenges

International Nuclear Information System (INIS)

Fadeff, S.K.; Goheen, S.C.; Riley, R.G.

1994-01-01

Radiochemistry methods in Department of Energy Methods for Evaluating Environmental and Waste Management Samples (DOE Methods) add to the repertoire of other standard methods in support of U.S. Department of Energy environmental restoration and waste management (DOE/EM) radiochemical characterization activities. Current standard sources of radiochemistry methods are not always applicable for evaluating DOE/EM samples. Examples of current sources include those provided by the US Environmental Protection Agency, the American Society for Testing and Materials, Standard Methods for the Examination of Water and Wastewater, and Environmental Measurements Laboratory Procedures Manual (HASL-300). The applicability of these methods is generally limited to specific matrices (usually water), low-level radioactive samples, and a limited number of analytes. DOE Methods complements these current standard methods by addressing the complexities of EM characterization needs. The process for determining DOE/EM radiochemistry characterization needs is discussed. In this context of DOE/EM needs, the applicability of other sources of standard radiochemistry methods is defined, and gaps in methodology are identified. Current methods in DOE Methods and the EM characterization needs they address are discussed. Sources of new methods and the methods incorporation process are discussed. The means for individuals to participate in (1) identification of DOE/EM needs, (2) the methods incorporation process, and (3) submission of new methods are identified

ICP-MS applications for the analysis of geological materials and environmental samples

International Nuclear Information System (INIS)

Bendl, J.

1997-01-01

This work deals with applications of inductively coupled plasma - mass spectrometry applications for the analysis of geological materials and environmental samples. There are instrumentation, calibration, alternatives of sample introduction, interferences, trace elements analysis, rare earth elements and uranium and thorium, precious metals, isotopic analysis and environmental analysis discussed

Hanford Site Environmental Surveillance Master Sampling Schedule for Calendar Year 2005

Energy Technology Data Exchange (ETDEWEB)

Bisping, Lynn E.

2005-01-19

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest National Laboratory (PNNL) for the U.S. Department of Energy (DOE). Sampling is conducted to evaluate levels of radioactive and nonradioactive pollutants in the Hanford environs. This document contains the calendar year 2005 schedules for the routine and non-routine collection of samples for the Surface Environmental Surveillance Project (SESP) and Drinking Water Monitoring Project.

Radiation Target Area Sample Environmental Chamber (RTASEC), Phase I

Data.gov (United States)

National Aeronautics and Space Administration — Payload Systems Inc. proposes the Radiation Target Area Sample Environmental Chamber (RTASEC) as an innovative approach enabling radiobiologists to investigate the...

Mounting Thin Samples For Electrical Measurements

Science.gov (United States)

Matus, L. G.; Summers, R. L.

1988-01-01

New method for mounting thin sample for electrical measurements involves use of vacuum chuck to hold a ceramic mounting plate, which holds sample. Contacts on mounting plate establish electrical connection to sample. Used to make electrical measurements over temperature range from 77 to 1,000 K and does not introduce distortions into magnetic field during Hall measurements.

Measurement of technetium-99 in Marshall Islands soil samples by ICP-MS

Science.gov (United States)

Tagami; Uchida; Hamilton; Robison

2000-07-01

Extraction techniques for recovery of technetium-99 (99Tc) for Inductively Coupled Plasma Mass Spectrometry (ICP-MS) measurements were evaluated using soil samples collected from the Marshall Islands. The results of three different extraction techniques were compared: (MI) acid leaching of Tc from ashed soil; (M2) acid leaching of Tc from raw dry soil; and (M3) Tc volatilization from ashed soil using a combustion apparatus. Total Tc recoveries varied considerably between the extraction techniques but each method yielded similar analytical results for 99Tc. Applications of these extraction techniques to a series of environmental samples and ICP-MS measurements have yielded first data on the 99Tc content of Marshall Islands soil samples contaminated with close-in radioactive fallout from nuclear weapons testing. The 99Tc activity concentration in the soil samples ranged between 0.1 and 1.1 mBq g(-1) dry weight (dw). The limit of detection for 99Tc by ICP-MS was 0.17 mBq per sample or 0.014 mBq g(-1) dw under standard operating conditions.

Measurement of technetium-99 in Marshall Islands soil samples by ICP-MS

International Nuclear Information System (INIS)

Tagami, K.; Uchida, S.; Hamilton, T.; Robison, W.

2000-01-01

Extraction techniques for recovery of technetium-99 ( 99 Tc) for Inductively Coupled Plasma Mass Spectrometry (ICP-MS) measurements were evaluated using soil samples collected from the Marshall Islands. The results of three different extraction techniques were compared: (M1) acid leaching of Tc from ashed soil; (M2) acid leaching of Tc from raw dry soil; and (M3) Tc volatilization from ashed soil using a combustion apparatus. Total Tc recoveries varied considerably between the extraction techniques but each method yielded similar analytical results for 99 Tc. Applications of these extraction techniques to a series of environmental samples and ICP-MS measurements have yielded first data on the 99 Tc content of Marshall Islands soil samples contaminated with close-in radioactive fallout from nuclear weapons testing. The 99 Tc activity concentration in the soil samples ranged between 0.1 and 1.1 mBq g -1 dry weight (dw). The limit of detection for 99 Tc by ICP-MS was 0.17 mBq per sample or 0.014 mBq g -1 dw under standard operating conditions

A study on identification of bacteria in environmental samples using single-cell Raman spectroscopy: feasibility and reference libraries.

Science.gov (United States)

Baritaux, Jean-Charles; Simon, Anne-Catherine; Schultz, Emmanuelle; Emain, C; Laurent, P; Dinten, Jean-Marc

2016-05-01

We report on our recent efforts towards identifying bacteria in environmental samples by means of Raman spectroscopy. We established a database of Raman spectra from bacteria submitted to various environmental conditions. This dataset was used to verify that Raman typing is possible from measurements performed in non-ideal conditions. Starting from the same dataset, we then varied the phenotype and matrix diversity content included in the reference library used to train the statistical model. The results show that it is possible to obtain models with an extended coverage of spectral variabilities, compared to environment-specific models trained on spectra from a restricted set of conditions. Broad coverage models are desirable for environmental samples since the exact conditions of the bacteria cannot be controlled.

Environmental radioactivity intercomparison measurements

International Nuclear Information System (INIS)

2000-01-01

In the context of the North Cotentin radioecological group set up in 1997 by the Ministry of the Environment and the Ministry of the Secretariat d'Etat a la Sante, the Swiss Federal Office of Public health, a national organization of independent status with respect to nuclear energy, conducted a series of measurements in the north Cotentin in 1998. Some sites proposed by local association 'Angry mothers' were examined in particular. This association has now taken the initiative to organize a large scale international intercomparison, ' North Cotentin 2000', in the vicinity of local nuclear installations. Besides the scientific aspect of the intercomparison, a specific aim of this intercomparison consists in providing to the local population with a real opportunity for direct exchange with participating international teams. The primary concern of the workshop is the determination, by in situ gamma spectrometry, of both natural and artificial concentrations and resulting ambient dose rates at selected marine ( beach) and terrestrial sites. A particular aim of the workshop also is to test the capacity of mobile teams to produce reliable results in the field of low level measurements on trace of special radionuclides (I 129 , Sr 90 , H 3 , C 14 , and alpha emitters) from environmental samples, using both direct ( in situ) and differed ( laboratory methods). an overview of the results obtained will be prepared for the benefit of the public. (N.C.)

Sampling, storage and sample preparation procedures for X ray fluorescence analysis of environmental materials

International Nuclear Information System (INIS)

1997-06-01

X ray fluorescence (XRF) method is one of the most commonly used nuclear analytical technique because of its multielement and non-destructive character, speed, economy and ease of operation. From the point of view of quality assurance practices, sampling and sample preparation procedures are the most crucial steps in all analytical techniques, (including X ray fluorescence) applied for the analysis of heterogeneous materials. This technical document covers recent modes of the X ray fluorescence method and recent developments in sample preparation techniques for the analysis of environmental materials. Refs, figs, tabs

The application of x-ray fluorescence and diffraction to the characterization of environmental assessment samples

International Nuclear Information System (INIS)

Censullo, A.C.; Briden, F.E.

1982-01-01

Some of the results of tests on environmental assessment samples are reported on. The utility of the J.W. Criss fundamental parameters computer program is evaluated for samples in which only one standard per element was used and where the standard matrix did not strictly resemble the unknown matrix. The environmental significance of a sample is dependent not only on its elemental composition, but also on the species or phases which the elements comprise. X-ray powder diffraction may be used to advantage for speciation. Multi-phase environmental assessment samples are amenable to XRD interpretation. Some results of the application of the Joint Committee on Power Diffraction Standards computer interpretatin of typical environmental samples are discussed. They were shown to contribute to the specification of the complex samples that are encountered in environmental assessments

Time efficiency of tritium measurement in the environmental water by electrolysis enrichment (2)

International Nuclear Information System (INIS)

Ogata, Y.; Koganezawa, T.; Iida, T.

2003-01-01

Now the electrolysis enrichment is necessary for tritium measurement of the environmental water in Japan. Generally, the electrolysis needs distilling the sample water before and after the electrolysis. To save the time to measure, it was investigated that a possibility of the omission of the distillation after the electrolysis and of the substitution the filtration for the distillation before the electrolysis. The electrolysis was carried out with a device using solid polymer electrolyte layer, which was recently developed in Japan. Initially, impurities eluted from the device were measured by enrichment of ultra pure water. Although some impurities eluted from the layer, the concentrations were so low that the enriched water brought ineffectual quenching for the liquid scintillation counting. Secondly, two filtration methods, i.e.; micro filtration with the pore size of 0.1 μm and reverse osmosis, were applied to eliminate the impurities in the environmental waters before the electrolysis. Although the impurity concentrations in the samples by the filtrations were higher than those by the distillation, the filtered water brought only slight quenching. However, the frequent electrolysis of the water treated with the micro filtration caused degradation of the electrolysis cell. Consequently, the distillation after the electrolysis may omit, and the reverse osmosis treatment may alternate the distillation before the electrolysis. Improving the treatment will not only save the time and labor but also reduce the error with the treatment. The measurement technique proposed here will take 25 hours to measure one sample using the electrolysis device produced commercially. A hypothetic electrolysis device of which final sample volume were 20 cm 3 could allow the measuring time of 10 hours. (author)

Intercomparison of Environmental Nuclear Radiation Measuring

Institute of Scientific and Technical Information of China (English)

GAO; Fei; NI; Ning; HOU; Jin-bing; SONG; Ming-zhe

2015-01-01

In 2015,Radiation Metrology Division of China Institute of Atomic Energy organized an environmental monitoring of nuclear radiation measuring intercomparison,and 9laboratories attended.The intercomparison included environmental level dosemeters and protection level

Environmental pollution measurements and countermeasures

International Nuclear Information System (INIS)

Schuetz, M.

1994-01-01

This book gives the interested layman an insight into fundamental processes of ecology and closes the gap between theory and practice. The practical part shows how measuring instruments for environmental applications work, how errors of measurement can be avoided, and how to make use of the measured results. (orig./EF) [de

Measuring environmental attitudes of elementary school students

Science.gov (United States)

John C. Benjamin; George H. Moeller; Douglas A. Morrison

1977-01-01

A modified semantic differential was developed to measure environmental attitudes of sixth-graders. Classes were selected to represent different socioeconomic and residence backgrounds and degrees of previous exposure to structured environmental programs. Results indicate that: exposure to environmental education fosters favorable environmental attitudes; socioeconomic...

Determination of uranium and its isotopic ratios in environmental samples

International Nuclear Information System (INIS)

Flues Szeles, M.S.M.

1990-01-01

A method for the determination of uranium and its isotopic ratios ( sup(235)U/ sup(238)U and sup(234U/ sup(238)U) is established in the present work. The method can be applied in environmental monitoring programs of uranium enrichment facilities. The proposed method is based on the alpha spectrometry technique which is applied after a purification of the sample by using an ionic exchange resin. The total yield achieved was (91 + 5)% with a precision of 5%, an accuracy of 8% and a lower limit of detection of 7,9 x 10 sup(-4)Bq. The uranium determination in samples containing high concentration of iron, which is an interfering element present in environmental samples, particularly in soil and sediment, was also studied. The results obtained by using artificial samples containing iron and uranium in the ratio 1000:1, were considered satisfactory. (author)

Environmental distributions and the practical utilisation of detection limited environment measurement data

International Nuclear Information System (INIS)

Daniels, W.M.; Higgins, N.A.

2002-01-01

This study investigated methods of providing summary statistics for measurements of radioactive contamination in food when the available measurements are incomplete. Several techniques to calculate, for instance, the mean level of contamination when a significant number of samples are found to have less than the minimum level reported by measurements, are discussed. To support the estimation of summary statistics the study identifies physical processes that give rise to observed distributions, eg lognormal for the range of radioactivity levels found in environmental and food samples. The improved estimates possible by application of the methods reviewed will allow the Food Standards Agency to gain a better understanding of the levels of radioactivity in the environment and if required direct effort to minimising the most significant uncertainties in these estimates. The Ministry of Agriculture, Fisheries and Food, Radiological Safety and Nutrition Division (now part of the Food Standards Agency) funded this study, under contract RP0342. This work was undertaken under the Environmental Assessments and Emergency Response Group's Quality Management System, which has been approved by Lloyd's Register Quality Assurance to the Quality Management Standards ISO 9001:2000 and TickIT Guide Issue 5, certificate number 956546. (author)

Direct detection of Mycobacterium avium in environmental water and scale samples by loop-mediated isothermal amplification.

Science.gov (United States)

Nishiuchi, Yukiko; Tamaru, Aki; Suzuki, Yasuhiko; Kitada, Seigo; Maekura, Ryoji; Tateishi, Yoshitaka; Niki, Mamiko; Ogura, Hisashi; Matsumoto, Sohkichi

2014-06-01

We previously demonstrated the colonization of Mycobacterium avium complex in bathrooms by the conventional culture method. In the present study, we aimed to directly detect M. avium organisms in the environment using loop-mediated isothermal amplification (LAMP), and to demonstrate the efficacy of LAMP by comparing the results with those obtained by culture. Our data showed that LAMP analysis has detection limits of 100 fg DNA/reaction for M. avium. Using an FTA(®) elute card, DNA templates were extracted from environmental samples from bathrooms in the residences of 29 patients with pulmonary M. avium disease. Of the 162 environmental samples examined, 143 (88%) showed identical results by both methods; 20 (12%) and 123 (76%) samples were positive and negative, respectively, for M. avium. Of the remaining 19 samples (12%), seven (5%) and 12 (7%) samples were positive by the LAMP and culture methods, respectively. All samples that contained over 20 colony forming units/primary isolation plate, as measured by the culture method, were also positive by the LAMP method. Our data demonstrate that the combination of the FTA elute card and LAMP can facilitate prompt detection of M. avium in the environment.

PIXE - Analysis for environmental and biological samples

International Nuclear Information System (INIS)

Baptista, G.B.

1980-04-01

The usefulness and accuracy of PIXE as an analytical tool in the study of trace elements in environmental samples of the Brazilian Cerrado are discussed. The report lists actual and forthcoming publications resulting from the study. The mechanism of exchange of elements in solution in water to aerosols has been investigated. For details of the procedure the reader is referred to an earlier report

Comparison of accelerator mass spectrometric measurement with liquid scintillation counting measurement for the determination of 14C in environmental samples

International Nuclear Information System (INIS)

Yasuike, Kaeko; Yamada, Yoshimune; Amano, Hikaru

2010-01-01

The concentrations of organically-bound 14 C in tree-ring cellulose of a Japanese Black Pine grown in Shika-machi (37.0 deg. N, 136.8 deg. E) and those of a Japanese Cedar grown in Kanazawa (36.5 deg. N, 136.7 deg. E), Japan, were analyzed for the ring-years from 1989 to 1998 by the accelerator mass spectrometric measurement. The results were compared with those of the same samples analyzed by the liquid scintillation counting measurement to determine the reliability of liquid scintillation counting measurement. An important result of this study is that the sensitivity and reproducibility of accelerator mass spectrometric measurement was almost equal to that of liquid scintillation counting measurement.

Relationship between accuracy and number of samples on statistical quantity and contour map of environmental gamma-ray dose rate. Example of random sampling

International Nuclear Information System (INIS)

Matsuda, Hideharu; Minato, Susumu

2002-01-01

The accuracy of statistical quantity like the mean value and contour map obtained by measurement of the environmental gamma-ray dose rate was evaluated by random sampling of 5 different model distribution maps made by the mean slope, -1.3, of power spectra calculated from the actually measured values. The values were derived from 58 natural gamma dose rate data reported worldwide ranging in the means of 10-100 Gy/h rates and 10 -3 -10 7 km 2 areas. The accuracy of the mean value was found around ±7% even for 60 or 80 samplings (the most frequent number) and the standard deviation had the accuracy less than 1/4-1/3 of the means. The correlation coefficient of the frequency distribution was found 0.860 or more for 200-400 samplings (the most frequent number) but of the contour map, 0.502-0.770. (K.H.)

Materials and Methods for Streamlined Laboratory Analysis of Environmental Samples, FY 2016 Report

Energy Technology Data Exchange (ETDEWEB)

Addleman, Raymond S. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Naes, Benjamin E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); McNamara, Bruce K. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Olsen, Khris B. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Chouyyok, Wilaiwan [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Willingham, David G. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Spigner, Angel C. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2016-11-30

evaluation). • Explored improvements to carbonate-peroxide rapid uranium extraction chemistry. • Evaluated new sampling materials and methods (in collaboration with ORNL). • Demonstrated successful ES extractions from standard and novel swipes for a wide range uranium compounds of interest including UO₂F₂ and UO₂(NO₃)₂, U₃O₈ and uranium ore concentrate. • Completed initial discussions with commercial suppliers of PTFE swipe materials. • Submitted one manuscript for publication. Two additional drafts are being prepared. Principal progress and accomplishments on Task 2, Optimize Materials and Methods for Direct SIMS Environmental Sample Analysis, are listed below. • Designed a SIMS swipe sample holder that retrofits into existing equipment and provides simple, effective, and rapid mounting of ES samples for direct assay while enabling automation and laboratory integration. • Identified preferred conductive sampling materials with better performance characteristics. • Ran samples on the new PNNL NWAL equivalent Cameca 1280 SIMS system. • Obtained excellent agreement between isotopic ratios for certified materials and direct SIMS assay of very low levels of LEU and HEU UO₂F₂ particles on carbon fiber sampling material. Sample activities range from 1 to 500 CPM (uranium mass on sample is dependent upon specific isotope ratio but is frequently in the subnanogram range). • Found that the presence of the UF molecular ions, as measured by SIMS, provides chemical information about the particle that is separate from the uranium isotopics and strongly suggests that those particles originated from an UF6 enrichment activity. • Submitted one manuscript for publication. Another manuscript is in preparation.

Implementation of Mass Spectrometry for Bulk Analysis of Environmental and Nuclear Material Inspection Samples

International Nuclear Information System (INIS)

Bulyha, S.; Cunningham, A.; Koepf, A.; Macsik, Z.; Poths, J.

2015-01-01

In the frame of the ECAS project (Enhancing Capabilities of Safeguards Analytical Services) the IAEA Office of Safeguards Analytical Services has implemented the latest-generation inductively coupled plasma mass spectrometers, or ICP-MS, for (i) bulk analysis of uranium and plutonium isotopes in environmental inspection samples and (ii) impurity analyzes in uranium samples. The measurement accuracy for n(U-235)/ n(U-238) ratios has been improved by approximately five times with the new multi-collector ICP-MS equipment. Use of modern ICP-MS enabled also an improvement of instrumental detection limits for U-233 and U-236 and Pu isotopes by at least one order of magnitude in comparison to the values, which had been achieved with the previously used methods. The improved accuracy and precision for isotope ratio measurements is mainly due to the higher sensitivity and the possibility to simultaneously detect several U isotopes with a multi-collector detector block. Implementation of the ICP-MS has also demonstrated a possibility for an increased sample throughput. In parallel to the implementation of the ICP-MS, a new version of the ''modified total evaporation'' (MTE) method has been developed for isotopic analysis of uranium samples by multi-collector thermal ionization mass spectrometry (TIMS). The MTE method provides a measurement performance which is, in particular for minor uranium isotopes, by several orders of magnitude superior compared to the commonly used ''total evaporation'' method. The new mass spectrometric techniques significantly improve the capability of the IAEA safeguards laboratories to detect the presence of non-natural uranium and plutonium isotopes in environmental swipe samples and to identify previously imperceptible differences in nuclear ''signatures''. Thus, they enhance the IAEA's ability to obtain independent, timely and quality-assured safeguards-relevant data and ensure

Reliability of environmental sampling culture results using the negative binomial intraclass correlation coefficient.

Science.gov (United States)

Aly, Sharif S; Zhao, Jianyang; Li, Ben; Jiang, Jiming

2014-01-01

The Intraclass Correlation Coefficient (ICC) is commonly used to estimate the similarity between quantitative measures obtained from different sources. Overdispersed data is traditionally transformed so that linear mixed model (LMM) based ICC can be estimated. A common transformation used is the natural logarithm. The reliability of environmental sampling of fecal slurry on freestall pens has been estimated for Mycobacterium avium subsp. paratuberculosis using the natural logarithm transformed culture results. Recently, the negative binomial ICC was defined based on a generalized linear mixed model for negative binomial distributed data. The current study reports on the negative binomial ICC estimate which includes fixed effects using culture results of environmental samples. Simulations using a wide variety of inputs and negative binomial distribution parameters (r; p) showed better performance of the new negative binomial ICC compared to the ICC based on LMM even when negative binomial data was logarithm, and square root transformed. A second comparison that targeted a wider range of ICC values showed that the mean of estimated ICC closely approximated the true ICC.

210Pb and 210Po determination in environmental samples using liquid scintillation counting and alpha spectrometry

International Nuclear Information System (INIS)

Sanchez, D.P.; Sanchez, A.M.; Vargas, M.J.

2002-01-01

A simple radiochemical procedure has been developed to determine 210 Pb and 210 Po in environmental samples. After adding 209 Po tracer and Pb carrier, an aliquot of the sample is decomposed by microwave digestion or by evaporation with mineral acids (depending on the expected activity of the sample). Part of the leaching solution must be used for 210 Po determination, preparing a polonium source by spontaneous deposition onto a nickel disk. The quantitative recoveries are determined using a standard 209 Po tracer, and the activity concentration is determined by isotopic dilution alpha spectrometry. The remaining part of the leaching solution is used for 210 Pb determination by means of two alternative methods: lead can be retained from 1.5 M HCl by the DOWEX 1 X 8, Cl - form resin in a chromatographic column, and stripped with deionised water, or it can be separated by solvent extraction as a lead bromide complex with the organic compound ALIQUAT-336 in toluene (this second method is used preferably in water samples). The Pb source for measurement is prepared by precipitation as oxalate and the chemical recovery determined by gravimetry. The activity concentration of 210 Pb is calculated from the spectra measured with a liquid scintillation spectrometer. Several certified material samples supplied by IAEA were analysed to check the procedure. The measured values for 210 Pb and 210 Po were in good agreement with the certified values presenting deviations lower than 5%. Several environmental samples (river and well waters and also sediments) from zones impacted by Uranium mine exploitation were analysed using the described procedure. The mean yields of Pb and Po were (70 ± 10)% and (81 ± 7)% for waters and (70 ± 12)% and (77 ± 8)% for sediments. (author)

Evaluation of the uncertainty of environmental measurements of radioactivity

International Nuclear Information System (INIS)

Heydorn, K.

2003-01-01

Full text: The almost universal acceptance of the concept of uncertainty has led to its introduction into the ISO 17025 standard for general requirements to testing and calibration laboratories. This means that not only scientists, but also legislators, politicians, the general population - and perhaps even the press - expect to see all future results associated with an expression of their uncertainty. Results obtained by measurement of radioactivity have routinely been associated with an expression of their uncertainty, based on the so-called counting statistics. This is calculated together with the actual result on the assumption that the number of counts observed has a Poisson distribution with equal mean and variance. Most of the nuclear scientific community has therefore assumed that it already complied with the latest ISO 17025 requirements. Counting statistics, however, express only the variability observed among repeated measurements of the same sample under the same counting conditions, which is equivalent to the term repeatability used in quantitative analysis. Many other sources of uncertainty need to be taken into account before a statement of the uncertainty of the actual result can be made. As the first link in the traceability chain calibration is always an important uncertainty component in any kind of measurement. For radioactivity measurements in particular we find that counting geometry assumes the greatest importance, because it is often not possible to measure a standard and a control sample under exactly the same conditions. In the case of large samples we have additional uncertainty components associated with sample heterogeneity and its influence on self-absorption and counting efficiency. In low-level environmental measurements we have an additional risk of sample contamination, but the most important contribution to uncertainty is usually the representativity of the sample being analysed. For uniform materials this can be expressed by the

Use of immunomagnetic separation for the detection of Desulfovibrio vulgaris from environmental samples

Energy Technology Data Exchange (ETDEWEB)

Chakraborty, R.; Hazen, T.C.; Joyner, D.C.; Kusel, K.; Singer, M.E.; Sitte, J.; Torok, T.

2011-04-15

Immunomagnetic separation (IMS) has proved highly efficient for recovering microorganisms from heterogeneous samples. Current investigation targeted the separation of viable cells of the sulfate-reducing bacterium, Desulfovibrio vulgaris. Streptavidin-coupled paramagnetic beads and biotin labeled antibodies raised against surface antigens of this microorganism were used to capture D. vulgaris cells in both bioreactor grown laboratory samples and from extremely low-biomass environmental soil and subsurface drilling samples. Initial studies on detection, recovery efficiency and viability for IMS were performed with laboratory grown D. vulgaris cells using various cell densities. Efficiency of cell isolation and recovery (i.e., release of the microbial cells from the beads following separation) was followed by microscopic imaging and acridine orange direct counts (AODC). Excellent recovery efficiency encouraged the use of IMS to capture Desulfovibrio spp. cells from low-biomass environmental samples. The environmental samples were obtained from a radionuclide-contaminated site in Germany and the chromium (VI)-contaminated Hanford site, an ongoing bioremediation project of the U.S. Department of Energy. Field deployable IMS technology may greatly facilitate environmental sampling and bioremediation process monitoring and enable transcriptomics and proteomics/metabolomics-based studies directly on cells collected from the field.

Evaluation of the readsorption of plutonium and americium in dynamic fractionations of environmental solid samples

DEFF Research Database (Denmark)

Petersen, Roongrat; Hou, Xiaolin; Hansen, Elo Harald

2008-01-01

A dynamic extraction system exploiting sequential injection (SI) for sequential extractions incorporating a specially designed extraction column is developed to fractionate radionuclides in environmental solid samples such as soils and sediments. The extraction column can contain a large amount...... of soil sample (up to 5 g), and under optimal operational conditions it does not give rise to creation of back pressure. Attention has been placed on studies of the readsorption problems during sequential extraction using a modified Standards, Measurements and Testing (SM&T) scheme with 4-step sequential...

[Detection of Cryptospordium spp. in environmental water samples by FTA-PCR].

Science.gov (United States)

Zhang, Xiao-Ping; Zhu, Qian; He, Yan-Yan; Jiang, Li; Jiang, Shou-Fu

2011-02-01

To establish a FTA-polymeras chain reaction (FTA-PCR) method in detection of Cryptospordium spp. in different sources of water. The semi automated immunomagnetic separation (IMS) of Cryptospordium oocysts in environmental water samples was performed firstly, and then genomic DNA of Cryptospordium oocysts was extracted by FTA filters disk. Oligonucleotide primers were designed based on the DNA fragment of the 18 S rRNA gene from C. parvum. Plate DNA was amplified with primers in PCR. The control DNA samples from Toxoplasma gondii,Sarcocystis suihominis, Echinococcus granulosus, and Clonorchis sinensis were amplified simultaneously. All PCR products were detected by agar electrophoresis dyed with ethidium bromide. The 446 bp fragment of DNA was detected in all samples of C. parvum, C. andersoni, and C. baileyi, while it was not detected in control groups in laboratory. No positive samples were found from 10 samples collected from tape water in 5 districts of Shanghai City by FTA-PCR. Nine positive samples were detected totally from 70 different environmental water samples, there were 0 out of 15 samples from the source of tape water, 2 out of 25 from the Huangpu River, 5 out of 15 from rivers around the animal farmers, 1 out of 9 from output water of contaminating water treatment factory, 1 out of 6 from the out gate of living contaminating water. The 446 bp fragment was detected from all the amplified positive water samples. FTA-PCR is an efficient method for gene detection of Cryptospordium oocysts, which could be used in detection of environmental water samples. The contamination degree of Cryptospordium oocysts in the river water around animal farms is high.

Environmental monitoring at the nuclear power plants and Studsvik 1992-1993. Results from measurements of radionuclide contents of environmental samples, and from random checks by SSI

International Nuclear Information System (INIS)

Bengtson, P.; Larsson, C.M.; Simenstad, P.; Suomela, J.

1995-09-01

Marine samples from the vicinity of the plants show elevated radionuclide concentrations, caused by discharges from the plants. Very low concentrations are noted in terrestrial samples. At several locations, the effects of the Chernobyl disaster still dominates. Control samples measured by SSI have confirmed the measurements performed by the operators. 8 refs, 6 tabs, 46 figs

Method of quantitative analysis of fluorine in environmental samples using a pure-Ge detector

International Nuclear Information System (INIS)

Sera, K.; Terasaki, K.; Saitoh, Y.; Itoh, J.; Futatsugawa, S.; Murao, S.; Sakurai, S.

2004-01-01

We recently developed and reported a three-detector measuring system making use of a pure-Ge detector combined with two Si(Li) detectors. The efficiency curve of the pure-Ge detector was determined as relative efficiencies to those of the existing Si(Li) detectors and accuracy of it was confirmed by analyzing a few samples whose elemental concentrations were known. It was found that detection of fluorine becomes possible by analyzing prompt γ-rays and the detection limit was found to be less than 0.1 ppm for water samples. In this work, a method of quantitative analysis of fluorine has been established in order to investigate environmental contamination by fluorine. This method is based on the fact that both characteristic x-rays from many elements and 110 keV prompt γ-rays from fluorine can be detected in the same spectrum. The present method is applied to analyses of a few environmental samples such as tealeaves, feed for domestic animals and human bone. The results are consistent with those obtained by other methods and it is found that the present method is quite useful and convenient for investigation studies on regional pollution by fluorine. (author)

The determination of plutonium isotopes in environmental samples

International Nuclear Information System (INIS)

Siripirom, Lopchai.

1983-01-01

The concentration of plutonium in environmental samples such as soil, water, and surface air in the middle part of Thailand were studied. The surface air were collected only at the fifth floor of the Office of Atomic Energy for Peace (OAEP). Plutonium-242 was used as a tracer. Soil and air samples were dissolved by pyrosulphate fusion, and plutonium was co-precipitated with barium sulfate. Then dissolved the precipitate in perchloric acid. Plutonium was extracted out by using solvent bis-(2-ethylhexyl) phosphoric acid (HDEHP). Plutonium in water samples were coprecipitated with iron (III) hydroxide and were dissolved in 8 M. nitric acid. Then the plutonium was separated out by using anion exchange resin, Dowex 1x4. After the solvent extraction or the anion exchange, plutonium was coprecipitated with cerous hydroxide. The activities of plutonium were measured by a surface barrier detector for about 24 hours. Lower limit of detection for 1,440 minutes is 0.012 pCi. These studies showed that only plutonium-239, 240 was observed. The range of activities of plutonium-239, 240 in soil were 0.002-0.157 pCi/g (dry), in water were 0.1-81 f Ci/l, and in air were 7-330 a Ci/m 3 . However, the plutonium concentrations in these studies are far below the maximum permissible concentration (MPC) recommended by International Commission on Radiological Protection (ICRP) for general population which is equal to 3x10 8 f Ci/l of water and 5x10 6 a Ci/m 3 of air

Measurement of technetium-99 in Marshall Islands soil samples by ICP-MS

Energy Technology Data Exchange (ETDEWEB)

Tagami, K. E-mail: k_tagami@nirs.go.jp; Uchida, S.; Hamilton, T.; Robison, W

2000-07-15

Extraction techniques for recovery of technetium-99 ({sup 99}Tc) for Inductively Coupled Plasma Mass Spectrometry (ICP-MS) measurements were evaluated using soil samples collected from the Marshall Islands. The results of three different extraction techniques were compared: (M1) acid leaching of Tc from ashed soil; (M2) acid leaching of Tc from raw dry soil; and (M3) Tc volatilization from ashed soil using a combustion apparatus. Total Tc recoveries varied considerably between the extraction techniques but each method yielded similar analytical results for {sup 99}Tc. Applications of these extraction techniques to a series of environmental samples and ICP-MS measurements have yielded first data on the {sup 99}Tc content of Marshall Islands soil samples contaminated with close-in radioactive fallout from nuclear weapons testing. The {sup 99}Tc activity concentration in the soil samples ranged between 0.1 and 1.1 mBq g{sup -1} dry weight (dw). The limit of detection for {sup 99}Tc by ICP-MS was 0.17 mBq per sample or 0.014 mBq g{sup -1} dw under standard operating conditions.

An Optimized Method for Quantification of Pathogenic Leptospira in Environmental Water Samples.

Science.gov (United States)

Riediger, Irina N; Hoffmaster, Alex R; Casanovas-Massana, Arnau; Biondo, Alexander W; Ko, Albert I; Stoddard, Robyn A

2016-01-01

Leptospirosis is a zoonotic disease usually acquired by contact with water contaminated with urine of infected animals. However, few molecular methods have been used to monitor or quantify pathogenic Leptospira in environmental water samples. Here we optimized a DNA extraction method for the quantification of leptospires using a previously described Taqman-based qPCR method targeting lipL32, a gene unique to and highly conserved in pathogenic Leptospira. QIAamp DNA mini, MO BIO PowerWater DNA and PowerSoil DNA Isolation kits were evaluated to extract DNA from sewage, pond, river and ultrapure water samples spiked with leptospires. Performance of each kit varied with sample type. Sample processing methods were further evaluated and optimized using the PowerSoil DNA kit due to its performance on turbid water samples and reproducibility. Centrifugation speeds, water volumes and use of Escherichia coli as a carrier were compared to improve DNA recovery. All matrices showed a strong linearity in a range of concentrations from 106 to 10° leptospires/mL and lower limits of detection ranging from Leptospira in environmental waters (river, pond and sewage) which consists of the concentration of 40 mL samples by centrifugation at 15,000×g for 20 minutes at 4°C, followed by DNA extraction with the PowerSoil DNA Isolation kit. Although the method described herein needs to be validated in environmental studies, it potentially provides the opportunity for effective, timely and sensitive assessment of environmental leptospiral burden.

Environmental Sampling FY03 Annual Report - Understanding the Movement of Mercury on the INEEL

International Nuclear Information System (INIS)

Michael L. Abbott

2003-01-01

Environmental mercury measurements were started in Fy-01 at the Idaho National Engineering Laboratory (INEEL) to monitor downwind impacts from on-going waste treatment operations at the Idaho Nuclear Technology and Engineering Center (INTEC) and to improve our scientific understanding of mercury fate and transport in this region. This document provides a summary of the sampling done in FY04. Continuous total gaseous mercury (TGM) measurements were made using a Tekran Model 2537A mercury vapor analyzer during October 2002 and from February through July 2003. The equipment was deployed in a self-contained field trailer at the Experimental Field Station (EFS) four kilometers downwind (northeast) of INTEC. Mercury surface-to-air flux measurements were made in October 2002 and from February through May 2003 to better understand the fate of the estimated 1500 kg of mercury emitted from 36 years of calciner operations at INTEC and to improve our scientific understanding of mercury environmental cycling in this region. Flux was measured using an INEEL-designed dynamic flux chamber system with a Tekran automated dual sampling (TADS) unit. Diel flux was positively correlated with solar radiation (r = 0.65), air temperature (r = 0.64), and wind speed (r = 0.38), and a general linear model for flux prediction at the INEEL was developed. Reactive gaseous mercury (RGM) was measured at EFS in July using a Tekran Model 1130 mercury speciation unit. Based on comparisons with other published data around the U.S., mercury air concentrations and surface flux rates directly downwind from INTEC were not distinguishable from remote area (non-industrial) background levels during the monitoring period

Performance Measurement und Environmental Performance Measurement

OpenAIRE

Sturm, Anke

2000-01-01

Die Zielsetzung der vorliegenden Dissertationsschrift besteht in der Entwicklung einer systematisierten Vorgehensweise, eines Controllingmodells, zur unternehmensinternen Umweltleistungsmessung. Das entwickelte Environmental Performance Measurement (EPM)-Modell umfaßt die fünf Stufen Festlegung der Ziele der Umweltleistungsmessung (1. Stufe), Erfassung der Umwelteinflüsse nach der ökologischen Erfolgsspaltung (2. Stufe), Bewertung der Umwelteinflüsse auf der Grundlage des qualitätszielbezogen...

Towards integrating environmental performance in divisional performance measurement

Directory of Open Access Journals (Sweden)

Collins C Ngwakwe

2014-08-01

Full Text Available This paper suggests an integration of environmental performance measurement (EPM into conventional divisional financial performance measures as a catalyst to enhance managers’ drive toward cleaner production and sustainable development. The approach is conceptual and normative; and using a hypothetical firm, it suggests a model to integrate environmental performance measure as an ancillary to conventional divisional financial performance measures. Vroom’s motivation theory and other literature evidence indicate that corporate goals are achievable in an environment where managers’ efforts are recognised and thus rewarded. Consequently the paper suggests that environmentally motivated managers are important to propel corporate sustainability strategy toward desired corporate environmental governance and sustainable economic development. Thus this suggested approach modestly adds to existing environmental management accounting (EMA theory and literature. It is hoped that this paper may provide an agenda for further research toward a practical application of the suggested method in a firm.

Radionuclides concentration in marine environmental samples along the coast of Vietnam

International Nuclear Information System (INIS)

Nguyen Trong Ngo; Nguyen Thanh Binh; Nguyen Van Phuc; Le Nhu Sieu; Truong Y; Mai Thi Huong; Nguyen Thi Linh; Nguyen Mong Sinh; Phan Son Hai; Le Ngoc Chung; Dang Duc Nhan; Nguyen Quang Long; Nguyen Hao Quang; Tran Tuyet Mai

2009-01-01

Studies on radioactivity inventories in environmental samples are necessary as they will serve as baseline data for assessing any environmental impact usage of nuclear-based activities. Approximately 700 data on 238 U, 232 Th, 226 Ra, 90 Sr, 137 Cs, 239,240 Pu activity concentrations in 150 samples i.e. sea water, sediment, fish, mollusc, crustaceans, oyster and weeds samples collected from 7 various locations in Vietnam (Hai Phong, Nghe An, Khanh Hoa, Ninh Thuan, Binh Thuan, Vung Tau, Tien Giang) throughout 1999-2008 are summarised and presented in this paper. Generally, the levels of artificial radionuclides in the studied marine environmental samples are lower as compared to other Asia-Pacific countries while naturally occurred radionuclides activity concentrations obtained were found to be in accordance with respective data from other studies within Pacific region. The radionuclides bioaccumulation factors studied in Red laver and oyster were mostly found to be high; therefore, further reinvestigation should be done for these biota that will be used as bio-fingerprint indicators in monitoring the marine environment from nuclear-based pollutions. The data set obtained from this study is available to the Asia-Pacific Marine Radioactivity Database. (author)

Optimisation of the measurement protocols of 129I and 129I/127I. Methodology establishment for the measurement in environmental matrices

International Nuclear Information System (INIS)

Frechou, C.

2000-01-01

129 I, is a natural long-lived isotope, with a half-life of 15,7 million years, also artificially produced in nuclear power plant. It is then released in the liquid and gaseous effluents of the nuclear fuel reprocessing plants. 129 I is integrated in all biological compartments at different activity levels, depending on their distance from the emission source and their ability to metabolize iodine. Performances of the different 129 I and 129 I/ 127 I measurement techniques available: Radiochemical Neutron Activation Analysis, Accelerator Mass Spectrometry, direct γ-X spectrometry and liquid scintillation were evaluated. Associated radiochemical preparation steps of the two first techniques were optimized and adapted to the characteristics of the major environmental matrices. In a first step, the radiochemical protocols were developed and validated. In a second step, intercomparison exercises have been lead on various environmental samples presenting different 129 I activity levels. They showed the good agreement between the results given by the three techniques on different environmental matrices with activities between 0,2 and 200 Bq.kg -1 dry weight. As a conclusion, a methodology for the measurement of 129 I and 129 I/ 127 I ratio in environmental samples is proposed. It includes a decisional diagram taking into account the characteristics of the matrices, the detection limits and the answer delay. A study on the losses of 129 I during the calcination of an algae was lead by direct γ-X spectrometry and application studies were made to measure 129 I levels in different biological compartments issued from various locations: 129 I activity interspecific variation in different species of seaweeds from the French channel coast under the relative influence of La Hague, 129 I levels in bovine thyroids from the Cotentin area and 129 I in vegetal samples collected around the nuclear reprocessing plant of Marcoule. (author)

An overview of sample preparation procedures for LC-MS multiclass antibiotic determination in environmental and food samples.

Science.gov (United States)

Moreno-Bondi, María Cruz; Marazuela, María Dolores; Herranz, Sonia; Rodriguez, Erika

2009-10-01

Antibiotics are a class of pharmaceuticals that are of great interest due to the large volumes of these substances that are consumed in both human and veterinary medicine, and due to their status as the agents responsible for bacterial resistance. They can be present in foodstuffs and in environmental samples as multicomponent chemical mixtures that exhibit a wide range of mechanisms of action. Moreover, they can be transformed into different metabolites by the action of microorganisms, as well as by other physical or chemical means, resulting in mixtures with higher ecotoxicities and risks to human health than those of the individual compounds. Therefore, there is growing interest in the availability of multiclass methods for the analysis of antimicrobial mixtures in environmental and food samples at very low concentrations. Liquid chromatography (LC) has become the technique of choice for multiclass analysis, especially when coupled to mass spectrometry (LC-MS) and tandem MS (LC-MS(2)). However, due to the complexity of the matrix, in most cases an extraction step for sample clean-up and preconcentration is required before analysis in order to achieve the required sensitivities. This paper reviews the most recent developments and applications of multiclass antimicrobial determination in environmental and food matrices, emphasizing the practical aspects of sample preparation for the simultaneous extraction of antimicrobials from the selected samples. Future trends in the application of LC-MS-based techniques to multiclass antibiotic analysis are also presented.

Middlesex Sampling Plant [MSP] annual site environmental report, calendar year 1988

International Nuclear Information System (INIS)

1989-04-01

The environmental monitoring program, which began in 1980, was continued in 1988 at the former Middlesex Sampling Plant (MSP) site, located in the Borough of Middlesex, New Jersey. The MSP site is part of the Formerly Utilized Site Remedial Action Program (FUSRAP), a Department of Energy (DOE) program to decontaminate or otherwise control sites where residual radioactive materials remain either from the early years of the nation's atomic energy program or from commercial operations causing conditions that Congress has mandated DOE to remedy. The environmental monitoring program is carried out by Bechtel National, Inc. (BNI), project management contractor for FUSRAP. The monitoring program at the MSP measures radon concentrations in air; external gamma radiation levels; and uranium and radium concentrations in surface water, groundwater, and sediment. To verify that the site is in compliance with the DOE radiation protection standard (100 mrem/yr) and to assess its potential effect on public health, the radiation dose was calculated for a hypothetical maximally exposed individual. Results of the 1988 monitoring show that the MSP is in compliance with applicable DOE radiation protection standards and with applicable requirements specified by New Jersey Department of Environmental Protection groundwater permits. 17 refs., 15 figs., 21 tabs

The sampling and analysing methods of radionuclides used in the Nordic countries for environmental samples

International Nuclear Information System (INIS)

Taipale, Tarja K.

1985-01-01

The Radioecology Group under the Nordic Liaison Committee for Atomic Energy has considered it to be of great importance to improve the comparability of environmental radioactivity measurements in the Nordic countries, a basic requirement for co-ordinated research programmes. In case of emergency, good comparability between the results obtained will be required for mutual assistance. Therefore several intercomparison exercises have been carried out between the laboratories measuring environmental radioactivity. The exercises have proved very useful and have led to a more comprehensive and systematic survey of the environmental measurement methodology used so far by the Nordic laboratories. Furthermore it is considered necessary to make some recommendations or even to reach an agreement on how to present the results in order to make the comparison of, at least, monitoring data easier. This report is based on the answers received from the participating laboratories to a questionnaire sent by the Finnish Centre for Radiation and Nuclear Safety, Helsinki

The sampling and analysing methods of radionuclides used in the Nordic countries for environmental samples

Energy Technology Data Exchange (ETDEWEB)

Taipale, Tarja K [ed.

1985-01-01

The Radioecology Group under the Nordic Liaison Committee for Atomic Energy has considered it to be of great importance to improve the comparability of environmental radioactivity measurements in the Nordic countries, a basic requirement for co-ordinated research programmes. In case of emergency, good comparability between the results obtained will be required for mutual assistance. Therefore several intercomparison exercises have been carried out between the laboratories measuring environmental radioactivity. The exercises have proved very useful and have led to a more comprehensive and systematic survey of the environmental measurement methodology used so far by the Nordic laboratories. Furthermore it is considered necessary to make some recommendations or even to reach an agreement on how to present the results in order to make the comparison of, at least, monitoring data easier. This report is based on the answers received from the participating laboratories to a questionnaire sent by the Finnish Centre for Radiation and Nuclear Safety, Helsinki.

The role of NAA in the environmental studies. Quantitative determination of heavy metals pollutant on environmental samples

International Nuclear Information System (INIS)

Sutisna; Yusuf, Saeful; Fisli, Adel; Rukihati; Wardhani, Sri; Th Rina M

2003-01-01

The neutron activation analysis technique was applied in the elemental analysis of environmental samples to solve an environmental pollution problem. We focused our study in the analysis of heavy metal which has potentially become a pollutant. The environmental samples analyzed were some water, sediment and an air particulate matter. The tap water sample was collected from five samplings points located at region of Serpong and Muria. Meanwhile the river water samples were taken from five samplings points of Ciliwung River. Eight samplings points of Cisadane river estuary located at Tanjung Burung were selected to collect sediment samples. Air particulate samples were collected from Jakarta Metropolitan and Serpong using high volume air sampler. Trace elements analyses of water samples were done using a combination of INAA and pre-concentration stage prior irradiation. All samples were irradiated at GA. Siwabessy reactor located at Serpong using a thermal neutron flux of about 10 12 n.cm -2 .sec -1 . After cooling time, the samples irradiated were counted by a high resolution HPGe detector coupled to a multichannel analyzer. The quantitative analyses have been done using a comparative method to a fresh laboratory standard and we used some standard references materials to validate our analytical result. The obtained result from the tap water analysis show that the elements of As, Cr, Co, Cd, Mn, Sb and Zn could be determine quantitatively and they have a concentration range from about 0.02 μg/L to 103.9 μg/L. The analysis result of Ciliwung river water samples show that elements of Ag, As, Co, Cu, Fe, Hg, Mn, V and Zn are present in the range of 2.4 μg/L to about 1365.8 μg/L. Meanwhile some important elements were obtained in the sediments samples taken from Cisadane River estuary such as Ce (40.4 - 63.6 mg/kg), Co (15.2 - 40.2 mg/kg), Cr (21.6 - 57.8 mg/kg), Eu (1.2 - 1.8 mg/kg), Fe (7.0 - 16.8 mg/kg), Mn (887 - 1810 mg/kg) and V (160 - 558 mg/kg). Finally the

Environmental radioactivity measurement. Ispra 1990

International Nuclear Information System (INIS)

Dominici, G.; Risposi, L.

1992-01-01

In this report there are briefly described the measurements of environmental radioactivity performed during 1990 by the site survey group of the Radioprotection Division at the Joint Research Centre Ispra Establishment. Data are give on the concentrations of Sr-90, Cs-137, HTO and other radionuclides in precipitation, air, waters, herbage, milk and radioactive effluents. The environmental contamination is mainly a consequence of the nuclear accident of Chernobyl

Nuclear techniques for analysis of environmental samples

International Nuclear Information System (INIS)

1986-12-01

The main purposes of this meeting were to establish the state-of-the-art in the field, to identify new research and development that is required to provide an adequate framework for analysis of environmental samples and to assess needs and possibilities for international cooperation in problem areas. This technical report was prepared on the subject based on the contributions made by the participants. A separate abstract was prepared for each of the 9 papers

Neutron activation analysis of 127I and 129I environmental samples

International Nuclear Information System (INIS)

Takeishi, Minoru; Namiki, Atsushi; Ishida, Junichiro; Iwai, Makoto

1987-01-01

The analytical method of 127 I and 129 I in environmental samples has been studied and the background levels of these nuclides in soils, seaweeds and milk were measured. The analytical method consists of the combustion technique and neutron activation analysis (N.A.A.). The iodine was separated from samples by ignition at about 1,000 deg C in a quartz combustion apparatus with an oxygen and a nitrogen stream, and was absorbed by small amounts of active charcoal. The iodine was then purified through the carbontetrachloride extraction method and the PdI 2 decomposition method. Irradiation was conducted by JRR-4 (n th : 8 x 10 13 n/cm 2 · sec) for 40 min. After irradiation, the iodine was purified by the solvent extraction method same as pre-irradiation extraction. Each activity of 126 I and 130 I, which was produced by 127 I(n,2n) 126 I and 129 I(n,γ) 130 I reaction respectively, was measured by γ-spectrometry using a Ge-detector. The lower detection limits of 129 I by this method were 4 x 10 -7 Bq/g for dry soil, 7 x 10 -8 Bq/g for fresh seaweeds and 7 x 10 -6 Bq/l for fresh milk, respectively. The relative standard deviation of 129 I measurements in soil and milk were less than 10 %. (author)

Systematic review and consensus guidelines for environmental sampling of Burkholderia pseudomallei.

Directory of Open Access Journals (Sweden)

Direk Limmathurotsakul

Full Text Available Burkholderia pseudomallei, a Tier 1 Select Agent and the cause of melioidosis, is a Gram-negative bacillus present in the environment in many tropical countries. Defining the global pattern of B. pseudomallei distribution underpins efforts to prevent infection, and is dependent upon robust environmental sampling methodology. Our objective was to review the literature on the detection of environmental B. pseudomallei, update the risk map for melioidosis, and propose international consensus guidelines for soil sampling.An international working party (Detection of Environmental Burkholderia pseudomallei Working Party (DEBWorP was formed during the VIth World Melioidosis Congress in 2010. PubMed (January 1912 to December 2011 was searched using the following MeSH terms: pseudomallei or melioidosis. Bibliographies were hand-searched for secondary references. The reported geographical distribution of B. pseudomallei in the environment was mapped and categorized as definite, probable, or possible. The methodology used for detecting environmental B. pseudomallei was extracted and collated. We found that global coverage was patchy, with a lack of studies in many areas where melioidosis is suspected to occur. The sampling strategies and bacterial identification methods used were highly variable, and not all were robust. We developed consensus guidelines with the goals of reducing the probability of false-negative results, and the provision of affordable and 'low-tech' methodology that is applicable in both developed and developing countries.The proposed consensus guidelines provide the basis for the development of an accurate and comprehensive global map of environmental B. pseudomallei.

Hanford Site Environmental Surveillance Master Sampling Schedule for Calendar Year 2011

Energy Technology Data Exchange (ETDEWEB)

Bisping, Lynn E.

2011-01-21

This document contains the calendar year 2011 schedule for the routine collection of samples for the Surface Environmental Surveillance Project and the Drinking Water Monitoring Project. Each section includes sampling locations, sampling frequencies, sample types, and analyses to be performed. In some cases, samples are scheduled on a rotating basis. If a sample will not be collected in 2011, the anticipated year for collection is provided. Maps showing approximate sampling locations are included for media scheduled for collection in 2011.

A sensitive analytical procedure for monitoring acrylamide in environmental water samples by offline SPE-UPLC/MS/MS.

Science.gov (United States)

Togola, Anne; Coureau, Charlotte; Guezennec, Anne-Gwenaëlle; Touzé, Solène

2015-05-01

The presence of acrylamide in natural systems is of concern from both environmental and health points of view. We developed an accurate and robust analytical procedure (offline solid phase extraction combined with UPLC/MS/MS) with a limit of quantification (20 ng L(-1)) compatible with toxicity threshold values. The optimized (considering the nature of extraction phases, sampling volumes, and solvent of elution) solid phase extraction (SPE) was validated according to ISO Standard ISO/IEC 17025 on groundwater, surface water, and industrial process water samples. Acrylamide is highly polar, which induces a high variability during the SPE step, therefore requiring the use of C(13)-labeled acrylamide as an internal standard to guarantee the accuracy and robustness of the method (uncertainty about 25 % (k = 2) at limit of quantification level). The specificity of the method and the stability of acrylamide were studied for these environmental media, and it was shown that the method is suitable for measuring acrylamide in environmental studies.

Spectrophotometric Determination of Boron in Environmental Water Samples

International Nuclear Information System (INIS)

San San; Khin Win Kyi; Kwaw Naing

2002-02-01

The present paper deals with the study on the methods for the determination of boron in the environmental water samples. The standard methods which are useful for this determination are discussed thoroughly in this work. Among the standard methods approved by American Public Health Association, the carmine method was selected for this study. Prior to the determination of boron in the water samples, the precision and accuracy of the methods of choice were examined by using standard boron solutions. The determination of Boron was carried out by using water samples, waste water from Aquaculture Research Centre, University of Yangon, the Ayeyarwady River water near Magway Myathalon Pagoda in Magway Division, ground water from Sanchaung Township, and tap water from Universities' Research Centre, University of Yangon. Analyses of these water samples were done and statistical treatment of the results was carried out. (author)

Radioisotope Sample Measurement Techniques in Medicine and Biology. Proceedings of the Symposium on Radioisotope Sample Measurement Techniques

International Nuclear Information System (INIS)

1965-01-01

The medical and biological applications of radioisotopes depend on two basically different types of measurements, those on living subjects in vivo and those on samples in vitro. The International Atomic Energy Agency has in the past held several meetings on in vivo measurement techniques, notably whole-body counting and radioisotope scanning. The present volume contains the Proceedings of the first Symposium the Agency has organized to discuss the various aspects of techniques for sample measurement in vitro. The range of these sample measurement techniques is very wide. The sample may weigh a few milligrams or several hundred grams, and may be in the gaseous, liquid or solid state. Its radioactive content may consist of a single, known radioisotope or several unknown ones. The concentration of radioactivity may be low, medium or high. The measurements may be made manually or automatically and any one of the many radiation detectors now available may be used. The 53 papers presented at the Symposium illustrate the great variety of methods now in use for radioactive- sample measurements. The first topic discussed is gamma-ray spectrometry, which finds an increasing number of applications in sample measurements. Other sections of the Proceedings deal with: the use of computers in gamma-ray spectrometry and multiple tracer techniques; recent developments in activation analysis where both gamma-ray spectrometry and computing techniques are applied; thin-layer and paper radio chromatographic techniques for use with low energy beta-ray emitters; various aspects of liquid scintillation counting techniques in the measurement of alpha- and beta-ray emitters, including chemical and colour quenching; autoradiographic techniques; calibration of equipment; and standardization of radioisotopes. Finally, some applications of solid-state detectors are presented; this section may be regarded as a preview of important future developments. The meeting was attended by 203 participants

Development for ultra-trace analysis method of U and Pu in safeguards environmental samples at the clean facility

International Nuclear Information System (INIS)

Takahashi, Masato; Magara, Masaaki; Sakurai, Satoshi

2002-01-01

Based on the strengthen safeguard program of the IAEA to detect undeclared nuclear activities and nuclear materials, the method of precise and accurate isotope ratio determination for uranium and plutonium in the environmental samples (cotton swipes) has been developed at JAERI. The samples should be treated in clean environment in order to secure the analytical reliability by eliminating external contamination from the samples containing trace amount of uranium and plutonium. Since the measurement by ICP-MS is favorable to bulk analysis from view points of analytical capacity and operation simplicity, we have studied sample preparation procedures for the trace amount of uranium and plutonium to be applied to ICP-MS. Up to the present, interfering factors involved during analytical processes and the ICP-MS measurement of uranium and plutonium were examined. As a result, uranium isotope measurement more than 100 pg became possible at JAERI clean facility by diminishing uranium blank introduced in the entire sample treatment procedure. And also, the estimation of plutonium recovery yield and uranium decontamination factor suggested the possibility in plutonium isotope measurement more than 100 fg. (author)

New developments in the extraction and determination of parabens in cosmetics and environmental samples. A review

International Nuclear Information System (INIS)

Ocaña-González, Juan Antonio; Villar-Navarro, Mercedes; Ramos-Payán, María; Fernández-Torres, Rut; Bello-López, Miguel Angel

2015-01-01

Highlights: • The analysis of parabens in cosmetics and environmental samples is reviewed. • Literature in this field from 1980 to 2003 is briefly discussed. • Determination and extraction methods in the last decade are discussed in-depth. - Abstract: Parabens are a family of synthetic esters of p-hydroxibenzoic acid widely used as preservatives in cosmetics and health-care products, among other daily-use commodities. Recently, their potential endocrine disrupting effects have raised concerns about their safety and their potential effects as emerging pollutants, leading to the regulation of the presence of parabens in commercial products by national and trans-national organizations. Also, this has led to an interest in developing sensible and reliable methods for their determination in environmental samples, cosmetics and health-care products. This paper is a comprehensive up-to-date review of the literature concerning the determination of parabens in environmental samples and cosmetic and health-care products. A brief revision of the literature concerning the traditional determination of parabens (1980–2003) is included, followed by an in-depth revision of the recent developments in both measurement and extraction methods for parabens in the last years (2003–2013). Finally, possible future perspectives in this field are proposed

New developments in the extraction and determination of parabens in cosmetics and environmental samples. A review

Energy Technology Data Exchange (ETDEWEB)

Ocaña-González, Juan Antonio; Villar-Navarro, Mercedes [Department of Analytical Chemistry, Faculty of Chemistry, Universidad de Sevilla, c/Prof. García González, s/n. 41012 Seville (Spain); Ramos-Payán, María [Department of Analytical Chemistry, Faculty of Chemistry, Universidad de Sevilla, c/Prof. García González, s/n. 41012 Seville (Spain); Department of Analytical Chemistry, Lineberguer Cancer Center, The University of North Carolina at Chapel Hill, NC (United States); Fernández-Torres, Rut [Department of Analytical Chemistry, Faculty of Chemistry, Universidad de Sevilla, c/Prof. García González, s/n. 41012 Seville (Spain); Research Centre of Health and Environment (CYSMA), University of Huelva (Spain); Bello-López, Miguel Angel, E-mail: mabello@us.es [Department of Analytical Chemistry, Faculty of Chemistry, Universidad de Sevilla, c/Prof. García González, s/n. 41012 Seville (Spain)

2015-02-09

Highlights: • The analysis of parabens in cosmetics and environmental samples is reviewed. • Literature in this field from 1980 to 2003 is briefly discussed. • Determination and extraction methods in the last decade are discussed in-depth. - Abstract: Parabens are a family of synthetic esters of p-hydroxibenzoic acid widely used as preservatives in cosmetics and health-care products, among other daily-use commodities. Recently, their potential endocrine disrupting effects have raised concerns about their safety and their potential effects as emerging pollutants, leading to the regulation of the presence of parabens in commercial products by national and trans-national organizations. Also, this has led to an interest in developing sensible and reliable methods for their determination in environmental samples, cosmetics and health-care products. This paper is a comprehensive up-to-date review of the literature concerning the determination of parabens in environmental samples and cosmetic and health-care products. A brief revision of the literature concerning the traditional determination of parabens (1980–2003) is included, followed by an in-depth revision of the recent developments in both measurement and extraction methods for parabens in the last years (2003–2013). Finally, possible future perspectives in this field are proposed.

Environmental Uncertainty, Performance Measure Variety and Perceived Performance in Icelandic Companies

DEFF Research Database (Denmark)

Rikhardsson, Pall; Sigurjonsson, Throstur Olaf; Arnardottir, Audur Arna

and the perceived performance of the company. The sample was the 300 largest companies in Iceland and the response rate was 27%. Compared to other studies the majority of the respondents use a surprisingly high number of different measures – both financial and non-financial. This made testing of the three......The use of performance measures and performance measurement frameworks has increased significantly in recent years. The type and variety of performance measures in use has been researched in various countries and linked to different variables such as the external environment, performance...... measurement frameworks, and management characteristics. This paper reports the results of a study carried out at year end 2013 of the use of performance measures by Icelandic companies and the links to perceived environmental uncertainty, management satisfaction with the performance measurement system...

Estimating the uncertainty from sampling in pollution crime investigation: The importance of metrology in the forensic interpretation of environmental data.

Science.gov (United States)

Barazzetti Barbieri, Cristina; de Souza Sarkis, Jorge Eduardo

2018-07-01

The forensic interpretation of environmental analytical data is usually challenging due to the high geospatial variability of these data. The measurements' uncertainty includes contributions from the sampling and from the sample handling and preparation processes. These contributions are often disregarded in analytical techniques results' quality assurance. A pollution crime investigation case was used to carry out a methodology able to address these uncertainties in two different environmental compartments, freshwater sediments and landfill leachate. The methodology used to estimate the uncertainty was the duplicate method (that replicates predefined steps of the measurement procedure in order to assess its precision) and the parameters used to investigate the pollution were metals (Cr, Cu, Ni, and Zn) in the leachate, the suspect source, and in the sediment, the possible sink. The metal analysis results were compared to statutory limits and it was demonstrated that Cr and Ni concentrations in sediment samples exceeded the threshold levels at all sites downstream the pollution sources, considering the expanded uncertainty U of the measurements and a probability of contamination >0.975, at most sites. Cu and Zn concentrations were above the statutory limits at two sites, but the classification was inconclusive considering the uncertainties of the measurements. Metal analyses in leachate revealed that Cr concentrations were above the statutory limits with a probability of contamination >0.975 in all leachate ponds while the Cu, Ni and Zn probability of contamination was below 0.025. The results demonstrated that the estimation of the sampling uncertainty, which was the dominant component of the combined uncertainty, is required for a comprehensive interpretation of the environmental analyses results, particularly in forensic cases. Copyright © 2018 Elsevier B.V. All rights reserved.

Measuring Values in Environmental Research: A Test of an Environmental Portrait Value Questionnaire

Science.gov (United States)

Bouman, Thijs; Steg, Linda; Kiers, Henk A. L.

2018-01-01

Four human values are considered to underlie individuals’ environmental beliefs and behaviors: biospheric (i.e., concern for environment), altruistic (i.e., concern for others), egoistic (i.e., concern for personal resources) and hedonic values (i.e., concern for pleasure and comfort). These values are typically measured with an adapted and shortened version of the Schwartz Value Survey (SVS), to which we refer as the Environmental-SVS (E-SVS). Despite being well-validated, recent research has indicated some concerns about the SVS methodology (e.g., comprehensibility, self-presentation biases) and suggested an alternative method of measuring human values: The Portrait Value Questionnaire (PVQ). However, the PVQ has not yet been adapted and applied to measure values most relevant to understand environmental beliefs and behaviors. Therefore, we tested the Environmental-PVQ (E-PVQ) – a PVQ variant of E-SVS –and compared it with the E-SVS in two studies. Our findings provide strong support for the validity and reliability of both the E-SVS and E-PVQ. In addition, we find that respondents slightly preferred the E-PVQ over the E-SVS (Study 1). In general, both scales correlate similarly to environmental self-identity (Study 1), energy behaviors (Studies 1 and 2), pro-environmental personal norms, climate change beliefs and policy support (Study 2). Accordingly, both methodologies show highly similar results and seem well-suited for measuring human values underlying environmental behaviors and beliefs. PMID:29743874

Neutron activation analysis for environmental sample in Thailand

International Nuclear Information System (INIS)

Busamongkol, Arporn; Nouchpramool, Sunun; Bunprapob, Supamatthree; Sumitra, Tatchai

2003-01-01

Neutron Activation Analysis has been applied for the trace elements analysis in environmental samples. Thirty three samples of airborne particulate were collected every week at Ongkharak Nuclear Research Center (ONRC) during the period of June 1998 to March 1999. The Ti, I, Mg, Na, V, K, Cl, Al, Mn, Ca, As, Sm, Sb, Br, La, Ce, Th, Cr, Cs, Sc, Rb, Fe, Zn and Co were analyzed by Neutron Activation Analysis utilizing 2 MW TRIGA MARK III research reactor. The certified reference materials 1632a and 1633a from National Bureau of Standard were select as standard. (author)

Hanford Site Environmental Surveillance Master Sampling Schedule for Calendar Year 2007

Energy Technology Data Exchange (ETDEWEB)

Bisping, Lynn E.

2007-01-31

This document contains the calendar year 2007 schedule for the routine collection of samples for the Surface Environmental Surveillance Project and Drinking Water Monitoring Project. Each section includes sampling locations, sampling frequencies, sample types, and analyses to be performed. In some cases, samples are scheduled on a rotating basis and may not be collected in 2007 in which case the anticipated year for collection is provided. Maps showing approximate sampling locations are included for media scheduled for collection in 2007.

A method to combine non-probability sample data with probability sample data in estimating spatial means of environmental variables

NARCIS (Netherlands)

Brus, D.J.; Gruijter, de J.J.

2003-01-01

In estimating spatial means of environmental variables of a region from data collected by convenience or purposive sampling, validity of the results can be ensured by collecting additional data through probability sampling. The precision of the pi estimator that uses the probability sample can be

Quality assurance and reference material requirements and considerations for environmental sample analysis in nuclear forensics

International Nuclear Information System (INIS)

Swindle, D.W. Jr.; Perrin, R.E.; Goldberg, S.A.; Cappis, J.

2002-01-01

Full text: High-sensitivity nuclear environmental sampling and analysis techniques have been proven in their ability to verify declared nuclear activities, as well as to assist in the detection of undeclared nuclear activities and facilities. Following the Gulf War, the capability and revealing power of environmental sampling and analysis techniques to support international safeguards was demonstrated and subsequently adopted by the International Atomic Energy Agency (IAEA) as routine safeguards measures in safeguards inspections and verifications. In addition to having been proved useful in international safeguards, environmental sampling and analysis techniques have demonstrated their utility in identifying the origins of 'orphaned' nuclear material, as well as the origin of intercepted smuggled nuclear material. Today, environmental sampling and analysis techniques are now being applied in six broad areas to support nonproliferation, disarmament treaty verification, national and international nuclear security, and environmental stewardship of weapons production activities. Consequently, more and more laboratories around the world are establishing capabilities or expanding capabilities to meet these growing applications, and as such requirements for quality assurance and control are increasing. The six areas are: 1) Nuclear safeguards; 2) Nuclear forensics/illicit trafficking; 3) Ongoing monitoring and verification (OMV); 4) Comprehensive Test Ban Treaty (CTBT); 5) Weapons dismantlement/materials disposition; and 6) Research and development (R and D)/environmental stewardship/safety. Application of environmental sampling and analysis techniques and resources to illicit nuclear material trafficking, while embodying the same basic techniques and resources, does have unique requirements for sample management, handling, protocols, chain of custody, archiving, and data interpretation. These requirements are derived from needs of how data from nuclear forensics

A study on aluminum determination in environmental samples by Neutron Activation Analysis

International Nuclear Information System (INIS)

Noyori, Amanda

2017-01-01

Aluminum determinations are of great interest since this element is toxic to humans and it is widely distributed in the environment. Besides, the determinations of this element by conventional analytical methods present difficulties due to sample contamination during the analyses. Neutron activation analysis (NAA) for Al determination presents advantages of fast analyses and of high sensitivity. However, NAA of Al does present problems of P and Si nuclear reaction interferences. Aluminum is determined by measuring 28 Al, formed in the reaction 27 Al (n, γ) 28 Al, the same radioisotope formed in reactions 31 P (n, α) 28 Al and 28 Si (n, p) 28 Al. The purpose of this study was to determine Al in environmental samples by NAA correcting these interferences using correction factors, and determining P and Si concentrations in the samples. In this study, certified reference materials and biomonitor samples (tree barks and lichen) were analyzed. Experimental procedure consisted of irradiating an aliquot of the sample at the IEA-R1 nuclear research reactor together with Al standard, followed by gamma ray spectrometry. Phosphorus was determined by measuring beta radiation of 32 P using a Geiger-Müller counter. Silicon was determined by epithermal neutron activation analysis and measuring 29 Al formed in the reaction 29 Si (n, p) 29 Al. Results obtained in the determination of Al, P and Si in the certified reference materials showed good precision and accuracy with |Z-score| ≤ 2. Aluminum results in the biomonitor samples varied from to 253 to 15783 μg g -1 . In the case of P its concentrations varied from 283 to 1946 μg g -1 . Silicon determinations in biomonitors varied from 0.11 to 7.8 %. The interference contribution rates in the analyses of the biomonitor samples were of the order of 2.0 % and this contribution depends on the relation between concentrations of interfering elements and of Al in the sample. Detection limit values of Al in the biomonitor analyses

A Bayesian approach to assess data from radionuclide activity analyses in environmental samples

International Nuclear Information System (INIS)

Barrera, Manuel; Lourdes Romero, M.; Nunez-Lagos, Rafael; Bernardo, Jose M.

2007-01-01

A Bayesian statistical approach is introduced to assess experimental data from the analyses of radionuclide activity concentration in environmental samples (low activities). A theoretical model has been developed that allows the use of known prior information about the value of the measurand (activity), together with the experimental value determined through the measurement. The model has been applied to data of the Inter-laboratory Proficiency Test organised periodically among Spanish environmental radioactivity laboratories that are producing the radiochemical results for the Spanish radioactive monitoring network. A global improvement of laboratories performance is produced when this prior information is taken into account. The prior information used in this methodology is an interval within which the activity is known to be contained, but it could be extended to any other experimental quantity with a different type of prior information available

The role of NAA in the environmental studies. Quantitative determination of heavy metals pollutant on environmental samples

Energy Technology Data Exchange (ETDEWEB)

Sutisna; Yusuf, Saeful; Fisli, Adel; Rukihati; Wardhani, Sri; Th Rina M [National Nuclear Energy Agency of Indonesia, Kawasan Puspiptek, Serpong (Indonesia)

2003-03-01

The neutron activation analysis technique was applied in the elemental analysis of environmental samples to solve an environmental pollution problem. We focused our study in the analysis of heavy metal which has potentially become a pollutant. The environmental samples analyzed were some water, sediment and an air particulate matter. The tap water sample was collected from five samplings points located at region of Serpong and Muria. Meanwhile the river water samples were taken from five samplings points of Ciliwung River. Eight samplings points of Cisadane river estuary located at Tanjung Burung were selected to collect sediment samples. Air particulate samples were collected from Jakarta Metropolitan and Serpong using high volume air sampler. Trace elements analyses of water samples were done using a combination of INAA and pre-concentration stage prior irradiation. All samples were irradiated at GA. Siwabessy reactor located at Serpong using a thermal neutron flux of about 10{sup 12} n.cm{sup -2}.sec{sup -1}. After cooling time, the samples irradiated were counted by a high resolution HPGe detector coupled to a multichannel analyzer. The quantitative analyses have been done using a comparative method to a fresh laboratory standard and we used some standard references materials to validate our analytical result. The obtained result from the tap water analysis show that the elements of As, Cr, Co, Cd, Mn, Sb and Zn could be determine quantitatively and they have a concentration range from about 0.02 {mu}g/L to 103.9 {mu}g/L. The analysis result of Ciliwung river water samples show that elements of Ag, As, Co, Cu, Fe, Hg, Mn, V and Zn are present in the range of 2.4 {mu}g/L to about 1365.8 {mu}g/L. Meanwhile some important elements were obtained in the sediments samples taken from Cisadane River estuary such as Ce (40.4 - 63.6 mg/kg), Co (15.2 - 40.2 mg/kg), Cr (21.6 - 57.8 mg/kg), Eu (1.2 - 1.8 mg/kg), Fe (7.0 - 16.8 mg/kg), Mn (887 - 1810 mg/kg) and V (160 - 558

Preparation of in-house calibration source for the use in radioactivity analysis of the environmental samples. Consideration of homogeneity

International Nuclear Information System (INIS)

Aba, A.; Ismaeel, A.

2013-01-01

An in-house reference material has been prepared in Kuwait Institute for Scientific Research radioecology laboratory, for quality control purposes of gamma spectrometer systems. The material contains a known amount of uranium ore reference material (prepared by the International Atomic Energy Agency and coded as IAEA-RGU-1) which is mixed with marine sediment collected from Kuwait bay. The IAEA-RGU-1 has been certified that it is in equilibrium state with the decay daughters, and stable to be used for quality control purposes. Nevertheless, the homogeneous distribution of the doped material with the prepared source should be verified. This has been examined using gamma spectrometry measurements in conjunction with analysis of variance statistical tools, Dixon, box plots and Grubbs tests. The calculated total uncertainty has been utilized to establish the recommended specific activity ranges of 226 Ra, 224 Th, 214 Pb, 214 Bi and 210 Pb radioisotopes in the prepared source. The obtained results showed that the estimated uncertainty arising from the sample inhomogeneity has a significant contribution in the total uncertainty. The stability control charts of the ultra-low background gamma spectrometry system demonstrated the suitability of the prepared material for the purpose of quality control. However, the emitted gamma-rays from the prepared source covers the required energy range for determination of natural and artificial radionuclides in different species of environmental samples such as marine sediment, soil samples, and samples contaminated by naturally occurring radioactive material produced by oil industry. In addition, the material might be used for system calibration in case its traceability is proven. The experimental data revealed the significance of the homogeneity in preparing environmental samples for radioactivity measurements; in particular when small sample quantities of environmental samples are required to be analyzed. (author)

Laser-Assisted Sampling Techniques in Combination with ICP-MS: A Novel Approach for Particle Analysis at the IAEA Environmental Samples Laboratory

International Nuclear Information System (INIS)

Dzigal, N.; Chinea-Cano, E.

2015-01-01

Researchers have found many applications for lasers. About two decades ago, scientists started using lasers as sample introduction instruments for mass spectrometry measurements. Similarly, lasers as micro-dissection tools have also been increasingly on demand in the fields of life sciences, materials science, forensics, etc. This presentation deals with the interception of these aforementioned laser-assisted techniques to the field of particle analysis. Historically, the use of a nanosecond laser to ablate material has been used in materials science. Recently, it has been proven that in the analysis of particulate materials the disadvantages associated with the utilization of nanosecond lasers such as overheating and melting of the sample are suppressed when using femtosecond lasers. Further, due to the length of a single laser shot, fs-LA allows a more controlled ablation to occur and therefore the sample plasma is more homogeneous and less mass-fractionation events are detected. The use of laser micro-dissection devices enables the physical segmentation of microsized artefacts previously performed by a laborious manual procedure. By combining the precision of the laser cutting inherent to the LMD technique together with a particle identification methodology, one can increase the efficiency of single particle isolation. Further, besides the increase in throughput of analyses, this combination enhances the signal-to-noise ratio by removing matrix particles effectively. Specifically, this contribution describes the use of an Olympus+MMI laser microdissection device in improving the sample preparation of environmental swipe samples and the installation of an Applied Spectra J200 fs-LA/LIBS (laser ablation/laser inducedbreakdown spectroscopy) system as a sample introduction device to a quadrupole mass spectrometer, the iCap Q from Thermofisher Scientific at the IAEA Environmental Samples Laboratory are explored. Preliminary results of the ongoing efforts for the

Demonstration and determination of submicroscopic particles of uranium in environmental samples

International Nuclear Information System (INIS)

Sihelska, K.; Lorincik, J.; Sus, F.; Vesela, D.

2016-01-01

In this work laboratories of the Centrum vyzkumu Rez, Ltd are presented. Fission track analysis (FTA) is used for analysis of uranium in environmental samples. Treatment of samples for FTA is described and some results ar presented. The method of SIMS is used, too.

Isotope dilution and sampling factors of the quality assurance and TQM of environmental analysis

International Nuclear Information System (INIS)

Macasek, F.

1999-01-01

Sampling and preparatory treatment of environmental objects is discussed from the view of their information content, functional speciation of the pollutant, statistical distribution treatment and uncertainty assessment. During homogenization of large samples, a substantial information may be lost and validity of environmental information becomes vague. Isotope dilution analysis is discussed as the most valuable tool for both validity of analysis and evaluation of samples variance. Data collection for a non-parametric statistical treatment of series of 'non-representative' sub-samples, and physico-chemical speciation of analyte may actually better fulfill criteria of similarity and representativeness. Large samples are often required due to detection limits of analysis, but the representativeness of environmental samples should by understood not only by the mean analyte concentration, but also by its spatial and time variance. Hence, heuristic analytical scenarios and interpretation of results must be designed by cooperation of environmentalists and analytical chemists. (author)

State of the art of environmentally friendly sample preparation approaches for determination of PBDEs and metabolites in environmental and biological samples: A critical review.

Science.gov (United States)

Berton, Paula; Lana, Nerina B; Ríos, Juan M; García-Reyes, Juan F; Altamirano, Jorgelina C

2016-01-28

Green chemistry principles for developing methodologies have gained attention in analytical chemistry in recent decades. A growing number of analytical techniques have been proposed for determination of organic persistent pollutants in environmental and biological samples. In this light, the current review aims to present state-of-the-art sample preparation approaches based on green analytical principles proposed for the determination of polybrominated diphenyl ethers (PBDEs) and metabolites (OH-PBDEs and MeO-PBDEs) in environmental and biological samples. Approaches to lower the solvent consumption and accelerate the extraction, such as pressurized liquid extraction, microwave-assisted extraction, and ultrasound-assisted extraction, are discussed in this review. Special attention is paid to miniaturized sample preparation methodologies and strategies proposed to reduce organic solvent consumption. Additionally, extraction techniques based on alternative solvents (surfactants, supercritical fluids, or ionic liquids) are also commented in this work, even though these are scarcely used for determination of PBDEs. In addition to liquid-based extraction techniques, solid-based analytical techniques are also addressed. The development of greener, faster and simpler sample preparation approaches has increased in recent years (2003-2013). Among green extraction techniques, those based on the liquid phase predominate over those based on the solid phase (71% vs. 29%, respectively). For solid samples, solvent assisted extraction techniques are preferred for leaching of PBDEs, and liquid phase microextraction techniques are mostly used for liquid samples. Likewise, green characteristics of the instrumental analysis used after the extraction and clean-up steps are briefly discussed. Copyright © 2015 Elsevier B.V. All rights reserved.

Study on trace element determination in liver samples of great-white-egret Ardea alba Linnaeus, 1758 (Ardeidae, Aves) for environmental contamination biomionitoring

International Nuclear Information System (INIS)

Silva, Rita de Cassia A.; Saiki, Mitiko

2009-01-01

Predatory birds such as herons have been used as bioindicators of pollution since they are at the top of their food webs. The tissues of these animals are analyzed for assessing environmental pollution caused by toxic elements. In the present study, adequate experimental conditions were established for determination of trace elements concentrations in the liver samples of Great-white-egret (Ardea alba Linnaeus, 1758) for further application of this specimens as a bioindicator of environmental contamination. Four liver samples were collected from Greatwhite- egrets found in the metropolitan region of Sao Paulo and were they analyzed by the method of neutron activation analysis (NAA). Concentrations of the elements Br, Co, Cs, Fe, Na, Rb, Se and Zn were measured in these liver tissues. The findings of this present study demonstrated that the established procedure for liver sample treatment was appropriate to obtain a homogeneous sample. The method of neutron activation analysis (NAA) was very promising for liver sample analysis for evaluation of environmental contamination. (author)

Study on trace element determination in liver samples of great-white-egret Ardea alba Linnaeus, 1758 (Ardeidae, Aves) for environmental contamination biomionitoring

Energy Technology Data Exchange (ETDEWEB)

Silva, Rita de Cassia A.; Saiki, Mitiko, E-mail: rcsilva@ipen.b, E-mail: mitiko@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

2009-07-01

Predatory birds such as herons have been used as bioindicators of pollution since they are at the top of their food webs. The tissues of these animals are analyzed for assessing environmental pollution caused by toxic elements. In the present study, adequate experimental conditions were established for determination of trace elements concentrations in the liver samples of Great-white-egret (Ardea alba Linnaeus, 1758) for further application of this specimens as a bioindicator of environmental contamination. Four liver samples were collected from Greatwhite- egrets found in the metropolitan region of Sao Paulo and were they analyzed by the method of neutron activation analysis (NAA). Concentrations of the elements Br, Co, Cs, Fe, Na, Rb, Se and Zn were measured in these liver tissues. The findings of this present study demonstrated that the established procedure for liver sample treatment was appropriate to obtain a homogeneous sample. The method of neutron activation analysis (NAA) was very promising for liver sample analysis for evaluation of environmental contamination. (author)

A comparison of some radionuclide contents in environmental samples

International Nuclear Information System (INIS)

Shiraishi, Kunio; Muramatsu, Yasuyuki; Nakajima, Toshiyuki; Yamamoto, Masayoshi; Los, I.P.; Kamarikov, I.Yu.; Buzinny, M.G.

1992-01-01

Global contamination by radionuclides was likely induced through the Chernobyl nuclear accident in 1986. Environmental samples such as fish, milk, total diet samples etc., collected in Kiev, in the vicinity of Chernobyl, and Mito city, Japan, were analyzed for six selected radionuclides. After samples were dry-ashed, radioactivities of Cs-137, Cs-134, K-40, Co-60, and Mn-54 were determined by gamma-ray spectroscopy with a germanium detector. Strontium-90 was determined by low-background beta-spectrometry after chemical separations by fuming nitric acid. Concentrations of radioactivities in the Kiev samples, in the vicinity of the Chernobyl, are shown below. For comparison, values obtained in Japan, including literature values, are shown in parentheses. Radioactivities in airborne dust were: Sr-90, 63 mBq/m 3 (0.001-0.1); Cs-137, 26 mBg/m 3 (0.001-1); Cs-134, 4 mBq/m 3 ; Co-60, 4 mBq/m 3 ; Mn-54, 2 mBq/m 3 . Radioactivities of milk were as follows; Sr-90, 0.25-1.2 Bq/liter (0.01-0.1); Cs-137, 6-77 Bq/liter (0.01-1); Cs-134, 2-8 Bq/liter. Radioactivities of Sr-90 and Cs-137 for fish (carp), were found to be 3-75 Bq/kg-fresh (0.76-0.98) and 46-2130 Bq/kg-fresh (<0.8), respectively. It was observed that the daily intake of Sr-90 and Cs-137 were 0.25 Bq (0.1) and 0.43 Bq (0.1) per person, respectively. Due to the small number of samples analyzed it is premature to draw a firm conclusion from this study. However, the levels of radionuclides in environmental samples were found to differ between Kiev and Mito with wide ranges depending on the samples. (author)

Advances in Radiocarbon Measurement of Water Samples

Energy Technology Data Exchange (ETDEWEB)

Janovics, R.; Molnar, M.; Major, I. [Institute of Nuclear Research (ATO MKI), Hungarian Academy of Sciences, H-4001 Debrecen (Hungary); Svetlik, I. [Department of Radiation Dosimetry, Nuclear Physics Institute AS CR, Prague (Czech Republic); Wacker, L. [Institute for Particle Physics, ETH Hoenggerberg, Zuerich (Switzerland)

2013-07-15

In this paper two very different and novel methods for the {sup 14}C measurement of water samples are presented. The first method uses direct absorption into a scintillation cocktail and a following liquid scintillation measurement. Typical sample size is 20-40 L and overall uncertainty is {+-} 2% for modern samples. It is a very cost effective and easy to use method based on a novel and simple static absorption process for the CO{sub 2} extracted from groundwater. The other very sensitive method is based on accelerator mass spectrometry (AMS) using a gas ion source. With a MICADAS type AMS system we demonstrated that you can routinely measure the {sup 14}C content of 1 mL of water sample with better than 1% precision (for a modern sample). This direct {sup 14}C AMS measurement of water takes less than 20 minutes including sample preparation. (author)

Stability of mercury concentration measurements in archived soil and peat samples

Science.gov (United States)

Navrátil, Tomáš; Burns, Douglas; Nováková, Tereza; Kaňa, Jiří; Rohovec, Jan; Roll, Michal; Ettler, Vojtěch

2018-01-01

Archived soil samples can provide important information on the history of environmental contamination and by comparison with recently collected samples, temporal trends can be inferred. Little previous work has addressed whether mercury (Hg) concentrations in soil samples are stable with long-term storage under standard laboratory conditions. In this study, we have re-analyzed using cold vapor atomic adsorption spectroscopy a set of archived soil samples that ranged from relatively pristine mountainous sites to a polluted site near a non-ferrous metal smelter with a wide range of Hg concentrations (6 - 6485 µg kg-1). Samples included organic and mineral soils and peats with a carbon content that ranged from 0.2 to 47.7%. Soil samples were stored in polyethylene bags or bottles and held in laboratory rooms where temperature was not kept to a constant value. Mercury concentrations in four subsets of samples were originally measured in 2000, 2005, 2006 and 2007, and re-analyzed in 2017, i.e. after 17, 12, 11 and 10 years of storage. Statistical analyses of either separated or lumped data yielded no significant differences between the original and current Hg concentrations. Based on these analyses, we show that archived soil and peat samples can be used to evaluate historical soil mercury contamination.

An environmental impact measure for nuclear fuel cycle evaluation

International Nuclear Information System (INIS)

Ahn, Joonhong

2004-01-01

Review of the models and measures for repository performance assessment has revealed that dedicated measures for environmental impacts need to be developed for the purpose of nuclear-fuel-cycle evaluation from the viewpoint of environmental impact minimization. The present study proposes the total toxicity index of released radionuclides that have accumulated in the region exterior to the repository as an environmental impact measure. The measure is quantitatively evaluated by a radionuclide transport model that incorporates the effects of canister-array configuration and the initial mass loading in the waste canister. With the measure, it is demonstrated that the environmental impact of the repository can be effectively reduced by reduction of the initial mass loading and change in the canister-array configuration in the repository. Environmental impacts of the mill tailings and the depleted uranium are as important as those from the high-level radioactive wastes repository. For a fair comparison of various fuel cycles, the sum of these impacts should be compared. (author)

Determination of uranium isotopes in environmental samples by anion exchange in sulfuric and hydrochloric acid media

International Nuclear Information System (INIS)

Popov, L.

2016-01-01

Method for determination of uranium isotopes in various environmental samples is presented. The major advantages of the method are the low cost of the analysis, high radiochemical yields and good decontamination factors from the matrix elements, natural and man-made radionuclides. The separation and purification of uranium is attained by adsorption with strong base anion exchange resin in sulfuric and hydrochloric acid media. Uranium is electrodeposited on a stainless steel disk and measured by alpha spectrometry. The analytical method has been applied for the determination of concentrations of uranium isotopes in mineral, spring and tap waters from Bulgaria. The analytical quality was checked by analyzing reference materials. - Highlights: • The method allows cost-effective determination of U isotopes. • High amounts of environmental samples can be analyzed. • High chemical yields, energy resolution and decontamination factors were achieved. • Uranium isotope concentrations in mineral waters from Bulgaria are presented.

Measuring the environmental awareness of young farmers

Science.gov (United States)

Kountios, G.; Ragkos, A.; Padadavid, G.; Hadjimitsis, D.

2017-09-01

Young farmers in Europe, especially the beneficiaries of Common Agricultural Policy (CAP) funding schemes, are considered as the ones who could ensure the sustainability of the European Model of Agriculture. Economic efficiency and competitiveness, aversion of depopulation of rural areas and environmental protection constitute some of the key objectives of the CAP and young farmers are expected to play a role to all of them. This study proposes a way of measuring the potential of young farmers to contribute to the latter objectives of the CAP by estimating their environmental attitudes. Data from a questionnaire survey of 492 Greek young farmers were used to design a latent construct measuring their environmental attitudes. The latent construct was designed by means of an Explanatory Factor Analysis (EFA) using the responses to a set of 12 Likert-scale items. The results the EFA yielded a latent construct with three factors related to "Environmental pollution and policies (EPP)", "Environmental factors and food quality (EFF)" and "Farming practices and the environment". These results were validated through a CFA where 8 items in total were categorized in the three factors (latent variables). The utilization of the latent construct for the effective implementation of CAP measures could ameliorate the relationships of agriculture and environment in general.

Zoonotic pathogens isolated from wild animals and environmental samples at two California wildlife hospitals.

Science.gov (United States)

Siembieda, Jennifer L; Miller, Woutrina A; Byrne, Barbara A; Ziccardi, Michael H; Anderson, Nancy; Chouicha, Nadira; Sandrock, Christian E; Johnson, Christine K

2011-03-15

To determine types and estimate prevalence of potentially zoonotic enteric pathogens shed by wild animals admitted to either of 2 wildlife hospitals and to characterize distribution of these pathogens and of aerobic bacteria in a hospital environment. Cross-sectional study. Fecal samples from 338 animals in 2 wildlife hospitals and environmental samples from 1 wildlife hospital. Fecal samples were collected within 24 hours of hospital admission. Environmental samples were collected from air and surfaces. Samples were tested for zoonotic pathogens via culture techniques and biochemical analyses. Prevalence of pathogen shedding was compared among species groups, ages, sexes, and seasons. Bacterial counts were determined for environmental samples. Campylobacter spp, Vibrio spp, Salmonella spp, Giardia spp, and Cryptosporidium spp (alone or in combination) were detected in 105 of 338 (31%) fecal samples. Campylobacter spp were isolated only from birds. Juvenile passerines were more likely to shed Campylobacter spp than were adults; prevalence increased among juvenile passerines during summer. Non-O1 serotypes of Vibrio cholerae were isolated from birds; during an oil-spill response, 9 of 10 seabirds screened were shedding this pathogen, which was also detected in environmental samples. Salmonella spp and Giardia spp were isolated from birds and mammals; Cryptosporidium spp were isolated from mammals only. Floors of animal rooms had higher bacterial counts than did floors with only human traffic. Potentially zoonotic enteric pathogens were identified in samples from several species admitted to wildlife hospitals, indicating potential for transmission if prevention is not practiced.

Dielectrophoretic sample preparation for environmental monitoring of microorganisms: Soil particle removal.

Science.gov (United States)

Fatoyinbo, Henry O; McDonnell, Martin C; Hughes, Michael P

2014-07-01

Detection of pathogens from environmental samples is often hampered by sensors interacting with environmental particles such as soot, pollen, or environmental dust such as soil or clay. These particles may be of similar size to the target bacterium, preventing removal by filtration, but may non-specifically bind to sensor surfaces, fouling them and causing artefactual results. In this paper, we report the selective manipulation of soil particles using an AC electrokinetic microfluidic system. Four heterogeneous soil samples (smectic clay, kaolinitic clay, peaty loam, and sandy loam) were characterised using dielectrophoresis to identify the electrical difference to a target organism. A flow-cell device was then constructed to evaluate dielectrophoretic separation of bacteria and clay in a continous flow through mode. The average separation efficiency of the system across all soil types was found to be 68.7% with a maximal separation efficiency for kaolinitic clay at 87.6%. This represents the first attempt to separate soil particles from bacteria using dielectrophoresis and indicate that the technique shows significant promise; with appropriate system optimisation, we believe that this preliminary study represents an opportunity to develop a simple yet highly effective sample processing system.

Radioactivity measurements of soil samples from Raichur of Karnataka, India

International Nuclear Information System (INIS)

Rajesh, S.; Kerur, B.R.; Anilkumar, S.

2016-01-01

Radiations present in environment comprise the terrestrial and extraterrestrial radiations. Natural radioactivity measurement, radiation monitoring of the region, dose assessment and interpretation of radiological related parameters are crucial aspects from the public awareness and environmental safety point of view. It is found that values of the radiological parameters obtained for samples in the study area were found within acceptable or permissible limits. The estimated gamma absorbed dose rate was found to be in the range 32 - 162 nGy h -1 . Higher dose rate than that of the normal dose rate were observed in the regions where granitic, granitic gneiss and schist outcrops were prominent area

Environmentally development sustainable Measurement

International Nuclear Information System (INIS)

Correa Pinzon, Hector Jaime

1996-01-01

One of the topics of more present time in the national and international environment has to do with the environment and all circumstances that surround it. The public accountants are involved direct or indirectly with the environmental handling, this profession has a great incidence in many aspects of this topic. The environmental development has to do with several such aspects as inequality and poverty, the incalculable human resource, the same environment, the social, political and cultural aspects and some indicators that have to do with the same development. All the proposals that they have to do with the environmental development they don't stop to be simply index normalized, it is to include non-monetary elements of the well being toward the leading of the development politicians. Such events as environmental costs, environmental control, industrial processes, human resources and others of great importance possess continuous and permanent relationship with the public accounting. For this reason it has been to analyze environmental aspects, with the purpose of investigating what documentation and advances exist in other countries, to be able to show some light to the interested, and this way to develop some hypotheses that can be in turn elements of integration technician-accountant jointly. The measurements of the entrance and the total product of nation, they give an extremely imperfect indication of their well -being. Besides the holes so well well-known of their covering, as the domestic work not remunerated, it is necessary to know at least another group of information to be able to emit a conclusive trial about the tendencies of the human well-being

Measuring environmental sustainability in agriculture: A composite environmental impact index approach.

Science.gov (United States)

Sabiha, Noor-E; Salim, Ruhul; Rahman, Sanzidur; Rola-Rubzen, Maria Fay

2016-01-15

The present study develops a composite environmental impact index (CEII) to evaluate the extent of environmental degradation in agriculture after successfully validating its flexibility, applicability and relevance as a tool. The CEII tool is then applied to empirically measure the extent of environmental impacts of High Yield Variety (HYV) rice cultivation in three districts of north-western Bangladesh for a single crop year (October, 2012-September, 2013). Results reveal that 27 to 69 per cent of the theoretical maximum level of environmental damage is created due to HYV rice cultivation with significant regional variations in the CEII scores, implying that policy interventions are required in environmentally critical areas in order to sustain agriculture in Bangladesh. Copyright © 2015 Elsevier Ltd. All rights reserved.

Middlesex Sampling Plant environmental report for calendar year 1992, 239 Mountain Avenue, Middlesex, New Jersey

International Nuclear Information System (INIS)

1993-05-01

This report describes the environmental surveillance program at the Middlesex Sampling Plant (MSP) and provides the results for 1992. The site, in the Borough of Middlesex, New Jersey, is a fenced area and includes four buildings and two storage piles that contain 50,800 m 3 of radioactive and mixed hazardous waste. More than 70 percent of the MSP site is paved with asphalt. The MSP facility was established in 1943 by the Manhattan Engineer District (MED) to sample, store, and/or ship uranium, thorium, and beryllium ores. In 1955 the Atomic Energy Commission (AEC), successor to MED, terminated the operation and later used the site for storage and limited sampling of thorium residues. In 1967 AEC activities ceased, onsite structures were decontaminated, and the site was certified for unrestricted use under criteria applicable at that time. In 1980 the US Department of Energy (DOE) initiated a multiphase remedial action project to clean up several vicinity properties onto which contamination from the plant had migrated. Material from these properties was consolidated into the storage piles onsite. Environmental surveillance of MSP began in 1980 when Congress added the site to DOE's Formerly Utilized Sites Remedial Action Program. The environmental surveillance program at MSP includes sampling networks for radon and thoron in air; external gamma radiation exposure; and radium-226, radium-228, thorium-230, thorium-232, and total uranium in surface water, sediment, and groundwater. Additionally, chemical analyses are performed to detect metals and organic compounds in surface water and groundwater and metals in sediments. This program assists in fulfilling th DOE policy of measuring and monitoring effluents from DOE activities and calculating hypothetical doses

Comparison of three analytical methods to measure the size of silver nanoparticles in real environmental water and wastewater samples

Energy Technology Data Exchange (ETDEWEB)

Chang, Ying-jie [Department of Agricultural Chemistry, National Taiwan University, Taipei 106, Taiwan (China); Shih, Yang-hsin, E-mail: yhs@ntu.edu.tw [Department of Agricultural Chemistry, National Taiwan University, Taipei 106, Taiwan (China); Su, Chiu-Hun [Material and Chemical Research Laboratories, Industrial Technology Research Institute, Hsinchu 310, Taiwan (China); Ho, Han-Chen [Department of Anatomy, Tzu-Chi University, Hualien 970, Taiwan (China)

2017-01-15

Highlights: • Three emerging techniques to detect NPs in the aquatic environment were evaluated. • The pretreatment of centrifugation to decrease the interference was established. • Asymmetric flow field flow fractionation has a low recovery of NPs. • Hydrodynamic chromatography is recommended to be a low-cost screening tool. • Single particle ICPMS is recommended to accurately measure trace NPs in water. - Abstract: Due to the widespread application of engineered nanoparticles, their potential risk to ecosystems and human health is of growing concern. Silver nanoparticles (Ag NPs) are one of the most extensively produced NPs. Thus, this study aims to develop a method to detect Ag NPs in different aquatic systems. In complex media, three emerging techniques are compared, including hydrodynamic chromatography (HDC), asymmetric flow field flow fractionation (AF4) and single particle inductively coupled plasma-mass spectrometry (SP-ICP-MS). The pre-treatment procedure of centrifugation is evaluated. HDC can estimate the Ag NP sizes, which were consistent with the results obtained from DLS. AF4 can also determine the size of Ag NPs but with lower recoveries, which could result from the interactions between Ag NPs and the working membrane. For the SP-ICP-MS, both the particle size and concentrations can be determined with high Ag NP recoveries. The particle size resulting from SP-ICP-MS also corresponded to the transmission electron microscopy observation (p > 0.05). Therefore, HDC and SP-ICP-MS are recommended for environmental analysis of the samples after our established pre-treatment process. The findings of this study propose a preliminary technique to more accurately determine the Ag NPs in aquatic environments and to use this knowledge to evaluate the environmental impact of manufactured NPs.

Comparison of three analytical methods to measure the size of silver nanoparticles in real environmental water and wastewater samples

International Nuclear Information System (INIS)

Chang, Ying-jie; Shih, Yang-hsin; Su, Chiu-Hun; Ho, Han-Chen

2017-01-01

Highlights: • Three emerging techniques to detect NPs in the aquatic environment were evaluated. • The pretreatment of centrifugation to decrease the interference was established. • Asymmetric flow field flow fractionation has a low recovery of NPs. • Hydrodynamic chromatography is recommended to be a low-cost screening tool. • Single particle ICPMS is recommended to accurately measure trace NPs in water. - Abstract: Due to the widespread application of engineered nanoparticles, their potential risk to ecosystems and human health is of growing concern. Silver nanoparticles (Ag NPs) are one of the most extensively produced NPs. Thus, this study aims to develop a method to detect Ag NPs in different aquatic systems. In complex media, three emerging techniques are compared, including hydrodynamic chromatography (HDC), asymmetric flow field flow fractionation (AF4) and single particle inductively coupled plasma-mass spectrometry (SP-ICP-MS). The pre-treatment procedure of centrifugation is evaluated. HDC can estimate the Ag NP sizes, which were consistent with the results obtained from DLS. AF4 can also determine the size of Ag NPs but with lower recoveries, which could result from the interactions between Ag NPs and the working membrane. For the SP-ICP-MS, both the particle size and concentrations can be determined with high Ag NP recoveries. The particle size resulting from SP-ICP-MS also corresponded to the transmission electron microscopy observation (p > 0.05). Therefore, HDC and SP-ICP-MS are recommended for environmental analysis of the samples after our established pre-treatment process. The findings of this study propose a preliminary technique to more accurately determine the Ag NPs in aquatic environments and to use this knowledge to evaluate the environmental impact of manufactured NPs.

Development of a direct observation Measure of Environmental Qualities of Activity Settings.

Science.gov (United States)

King, Gillian; Rigby, Patty; Batorowicz, Beata; McMain-Klein, Margot; Petrenchik, Theresa; Thompson, Laura; Gibson, Michelle

2014-08-01

The aim of this study was to develop an observer-rated measure of aesthetic, physical, social, and opportunity-related qualities of leisure activity settings for young people (with or without disabilities). Eighty questionnaires were completed by sets of raters who independently rated 22 community/home activity settings. The scales of the 32-item Measure of Environmental Qualities of Activity Settings (MEQAS; Opportunities for Social Activities, Opportunities for Physical Activities, Pleasant Physical Environment, Opportunities for Choice, Opportunities for Personal Growth, and Opportunities to Interact with Adults) were determined using principal components analyses. Test-retest reliability was determined for eight activity settings, rated twice (4-6wk interval) by a trained rater. The factor structure accounted for 80% of the variance. The Kaiser-Meyer-Olkin Measure of Sampling Adequacy was 0.73. Cronbach's alphas for the scales ranged from 0.76 to 0.96, and interrater reliabilities (ICCs) ranged from 0.60 to 0.93. Test-retest reliabilities ranged from 0.70 to 0.90. Results suggest that the MEQAS has a sound factor structure and preliminary evidence of internal consistency, interrater, and test-retest reliability. The MEQAS is the first observer-completed measure of environmental qualities of activity settings. The MEQAS allows researchers to assess comprehensively qualities and affordances of activity settings, and can be used to design and assess environmental qualities of programs for young people. © 2014 Mac Keith Press.

Quality assurance program for determining the radioactivity in environmental samples at the Institute of Nuclear Energy Research in Taiwan

International Nuclear Information System (INIS)

Gone, J.K.; Wang, T.W.

2000-01-01

Interest in determining radioactivity in environmental samples has increased considerably in recent years after the Chernobyl accident in 1986. Environmental monitoring programs have been set up in different countries to measure the trace amount of radionuclides in the environment, and quality of the analytical results on these samples is important because the regulation and safety concerns. A good quality assurance program is essential to provide accurate information for the regulatory body and environmentalists to set proper reactions to protect the environment, and a good analytical result is also important for scientists to determine the transfer of radionuclides between environmental matrices. The Institute of Nuclear Energy Research (lNER) in Taiwan has been working on radionuclide analysis in environmental samples for years, and it's environmental media radioanalytical laboratory (EMRAL) has recently upgraded its quality assurance program for the international standard ISO/lEC guide 25 requirements. The general requirements of lSO/lEC guide 25 has been adapted by the Chinese National Laboratory Accreditation (CNLA) of Taiwan, and CNLA is also a member of International Laboratory Accreditation Cooperation (ILAC) and Asia Pacific Laboratory Accreditation Cooperation (APLAC). This paper summarizes the quality assurance program of lNER's EMRAL. It covers both management and technical sections. These sections have ensured the quality of INER's EMRAL, and they can be applied to different laboratories in the future. (author)

Quality assurance program for determining the radioactivity in environmental samples at the Institute of Nuclear Energy Research in Taiwan

Energy Technology Data Exchange (ETDEWEB)

Gone, J.K. [TRR-II Project Team, Institute of Nuclear Energy Research, Taoyuan, Taiwan (China); Wang, T.W. [Division of Health Physics, Institute of Nuclear Energy Research, Taoyuan, Taiwan (China)

2000-05-01

Interest in determining radioactivity in environmental samples has increased considerably in recent years after the Chernobyl accident in 1986. Environmental monitoring programs have been set up in different countries to measure the trace amount of radionuclides in the environment, and quality of the analytical results on these samples is important because the regulation and safety concerns. A good quality assurance program is essential to provide accurate information for the regulatory body and environmentalists to set proper reactions to protect the environment, and a good analytical result is also important for scientists to determine the transfer of radionuclides between environmental matrices. The Institute of Nuclear Energy Research (lNER) in Taiwan has been working on radionuclide analysis in environmental samples for years, and it's environmental media radioanalytical laboratory (EMRAL) has recently upgraded its quality assurance program for the international standard ISO/lEC guide 25 requirements. The general requirements of lSO/lEC guide 25 has been adapted by the Chinese National Laboratory Accreditation (CNLA) of Taiwan, and CNLA is also a member of International Laboratory Accreditation Cooperation (ILAC) and Asia Pacific Laboratory Accreditation Cooperation (APLAC). This paper summarizes the quality assurance program of lNER's EMRAL. It covers both management and technical sections. These sections have ensured the quality of INER's EMRAL, and they can be applied to different laboratories in the future. (author)

Separation Techniques for Quantification of Radionuclides in Environmental Samples

Directory of Open Access Journals (Sweden)

Dusan Galanda

2009-01-01

Full Text Available The reliable and quantitative measurement of radionuclides is important in order to determine environmental quality and radiation safety, and to monitor regulatory compliance. We examined soil samples from Podunajske Biskupice, near the city of Bratislava in the Slovak Republic, for the presence of several natural (238U, 232Th, 40K and anthropogenic (137Cs, 90Sr, 239Pu, 240Pu, 241Am radionuclides. The area is adjacent to a refinery and hazardous waste processing center, as well as the municipal incinerator plant, and so might possess an unusually high level of ecotoxic metals. We found that the levels of both naturally occurring and anthropogenic radionuclides fell within the expected ranges, indicating that these facilities pose no radiological threat to the local environment. During the course of our analysis, we modified existing techniques in order to allow us to handle the unusually large and complex samples that were needed to determine the levels of 239Pu, 240Pu, and 241Am activity. We also rated three commercial techniques for the separation of 90Sr from aqueous solutions and found that two of them, AnaLig Sr-01 and Empore Extraction Disks, were suitable for the quantitative and reliable separation of 90Sr, while the third, Sr-Spec Resin, was less so. The main criterion in evaluating these methods was the chemical recovery of 90Sr, which was less than we had expected. We also considered speed of separation and additional steps needed to prepare the sample for separation.

Pursuit of improvement in uranium bulk analysis at the clear facility for safeguards environmental samples

International Nuclear Information System (INIS)

Sakurai, S.; Takahashi, M.; Sakakibara, T.; Magara, M.; Kurosawa, S.; Esaka, F.; Takai, K.; Watanabe, K.; Usuda, S.; Adachi, T.

2002-01-01

Full text: In order to contribute to the IAEA strengthened safeguards system, a project started in Japan Atomic Energy Research Institute (JAERI) in 1998. Consequently, a clean room facility called as CLEAR, the Clean Laboratory for Environmental Analysis and Research, was constructed in June 2001 at JAERI Tokai and the analytical techniques of ultra-trace nuclear materials in environmental samples are being developed. As for the bulk analysis, performance of inductively-coupled plasma mass spectrometry (ICP-MS) was mainly examined because sample preparation for ICP-MS is simpler than that for thermal ionization mass spectrometry (TIMS). Interference of polyatomic ion (such as PtAr + ) and coexisting element (such as Na) on the uranium ions, as well as mass bias caused by ICP-MS operating conditions, has been investigated for precise measurement on uranium isotope ratio. The authors have also studied on the uranium blanks during sample treatment process. The blank value below 10 pg uranium per sample treatment was obtained: dominant origins were elution from Teflon vessel surface in acid heating process of the sample to dry up. The work is in progress to minimize the blank. Compared with the process blank and the minimum uranium amount for isotope ratio measurement by ICP-MS (ca. 10 pg for natural uranium), the swipe cotton (Texwipe-304) which is currently used for IAEA Environmental Sampling includes much more amount of natural uranium in several nano-grams. If the amount of uranium collected on Texwipe-304 is small, sensitive and reliable measurement on isotope ratio will be impossible by bulk analysis. The authors are seeking alternative swipe materials with less amount of uranium. Recently, one of the authors devised an effective technique for recovery of uranium-containing particles from Texwipe-304. The technique, named as Vacuum Suction Method, uses a combination of polycarbonate membrane filters and a macro-pipette tip, which is connected to a vacuum pump

Environmental Measurements Laboratory 1994 annual report

Energy Technology Data Exchange (ETDEWEB)

Chieco, N.A. [ed.; Krey, P.W.; Beck, H.L.

1995-08-01

This report summarizes the activities of the Environmental Measurements Laboratory (EML) for the calendar year 1994 and it serves as an annual report to the Director of the Office of Energy Research (ER), the Associate Director and staff of the Office of Health and Environmental Research (OHER), the manager and staff of the Chicago Field Office, and the authors colleagues. Emphasized are the progress and accomplishments of the year, rather than future plans or expectations. The technical summaries are grouped according to the following seven general program areas: environmental radiation and radioactivity; radiation transport and dosimetry; environmental radon, thoron, and related aerosols; atmospheric and surface pollutant studies related to global climate change; atmospheric chemistry; metrology, consultation, and emergency response; environmental management. EML`s mission is to address important scientific questions concerning human health and environmental impacts. Through its multidisciplinary staff, EML conducts experimental and theoretical research on radioactive and other energy-related pollutants, and provides DOE and other federal agencies with the in-house capability to respond effectively and efficiently with regard to quality assurance activities, environmental issues and related national security issues.

Environmental Measurements Laboratory 1994 annual report

International Nuclear Information System (INIS)

Chieco, N.A.; Krey, P.W.; Beck, H.L.

1995-08-01

This report summarizes the activities of the Environmental Measurements Laboratory (EML) for the calendar year 1994 and it serves as an annual report to the Director of the Office of Energy Research (ER), the Associate Director and staff of the Office of Health and Environmental Research (OHER), the manager and staff of the Chicago Field Office, and the authors colleagues. Emphasized are the progress and accomplishments of the year, rather than future plans or expectations. The technical summaries are grouped according to the following seven general program areas: environmental radiation and radioactivity; radiation transport and dosimetry; environmental radon, thoron, and related aerosols; atmospheric and surface pollutant studies related to global climate change; atmospheric chemistry; metrology, consultation, and emergency response; environmental management. EML's mission is to address important scientific questions concerning human health and environmental impacts. Through its multidisciplinary staff, EML conducts experimental and theoretical research on radioactive and other energy-related pollutants, and provides DOE and other federal agencies with the in-house capability to respond effectively and efficiently with regard to quality assurance activities, environmental issues and related national security issues

Legacy Risk Measure for Environmental Waste

International Nuclear Information System (INIS)

Eide, S. A.; Nitschke, R. L.

2002-01-01

The Idaho National Engineering and Environmental Laboratory (INEEL) is investigating the development of a comprehensive and quantitative risk model framework for environmental management activities at the site. Included are waste management programs (high-level waste, transuranic waste, low-level waste, mixed low-level waste, spent nuclear fuel, and special nuclear materials), major environmental restoration efforts, major decontamination and decommissioning projects, and planned long-term stewardship activities. Two basic types of risk estimates are included: risks from environmental management activities, and long-term legacy risks from wastes/materials. Both types of risks are estimated using the Environment, Safety, and Health Risk Assessment Program (ESHRAP) developed at the INEEL. Given these two types of risk calculations, the following evaluations can be performed: risk evaluation of an entire program (covering waste/material as it now exists through disposal or other e nd states); risk comparisons of alternative programs or activities; comparisons of risk benefit versus risk cost for activities or entire programs; ranking of programs or activities by risk; ranking of wastes/materials by risk; evaluation of site risk changes with time as activities progress; and integrated performance measurement using indicators such as injury/death and exposure rates. This paper discusses the definition and calculation of legacy risk measures and associated issues. The legacy risk measure is needed to support three of the seven types of evaluations listed above: comparisons of risk benefit versus risk cost, ranking of wastes/materials by risk, and evaluation of site risk changes with time

Measurement of environmental radioactivity. Ispra 1977

International Nuclear Information System (INIS)

Dominici, G.

1979-01-01

In this report there are briefly described the measurements of environmental radioactivity performed during 1977 by the site survey group of the Protection Division of the Euratom joint Research Centre - Ispra Establishement. Data are given on the concentrations of 90 Sr, 137 Cs and other radionuclides in precipitation, air, waters, herbage, milk and radioactive effluents. The environmental contamination is mainly world-wide fall out

Measurements of environmental radioactivity, Ispra 1988

International Nuclear Information System (INIS)

Dominici, G.

1989-01-01

In this report there are briefly described the measurements of environmental radioactivity performed during 1988 by the site survey group of the Radioprotection Division at the Joint Research Centre Ispra Establishment. Data are given on the concentrations of Sr-90, Cs-137, and other radionuclides in precipitation, air, waters, herbage, milk and radioactive effluents. The environmental contamination is mainly a consequence of the nuclear accident of Chernobyl

Measurement of environmental radioactivity. Ispra 1976

International Nuclear Information System (INIS)

Dominici, G.

1977-01-01

In this report there are briefly described the measurements of environmental radioactivity performed during 1976 by the site survey group of the Protection Division of the Euratom Joint Research Centre - Ispra Establisment. Data are given on the concentrations of 90 Sr, 137 Cs and other radionuclides in precipitation, air, waters, herbage milk and radioactive effluents. The environmental contamination is mainly world-wide fall out

Mercury in Environmental and Biological Samples Using Online Combustion with Sequential Atomic Absorption and Fluorescence Measurements: A Direct Comparison of Two Fundamental Techniques in Spectrometry

Science.gov (United States)

Cizdziel, James V.

2011-01-01

In this laboratory experiment, students quantitatively determine the concentration of an element (mercury) in an environmental or biological sample while comparing and contrasting the fundamental techniques of atomic absorption spectrometry (AAS) and atomic fluorescence spectrometry (AFS). A mercury analyzer based on sample combustion,…

The effects of environmental variability and spatial sampling on the three-dimensional inversion problem.

Science.gov (United States)

Bender, Christopher M; Ballard, Megan S; Wilson, Preston S

2014-06-01

The overall goal of this work is to quantify the effects of environmental variability and spatial sampling on the accuracy and uncertainty of estimates of the three-dimensional ocean sound-speed field. In this work, ocean sound speed estimates are obtained with acoustic data measured by a sparse autonomous observing system using a perturbative inversion scheme [Rajan, Lynch, and Frisk, J. Acoust. Soc. Am. 82, 998-1017 (1987)]. The vertical and horizontal resolution of the solution depends on the bandwidth of acoustic data and on the quantity of sources and receivers, respectively. Thus, for a simple, range-independent ocean sound speed profile, a single source-receiver pair is sufficient to estimate the water-column sound-speed field. On the other hand, an environment with significant variability may not be fully characterized by a large number of sources and receivers, resulting in uncertainty in the solution. This work explores the interrelated effects of environmental variability and spatial sampling on the accuracy and uncertainty of the inversion solution though a set of case studies. Synthetic data representative of the ocean variability on the New Jersey shelf are used.

Modern systems for environmental radioactivity measurements

International Nuclear Information System (INIS)

Cimpean, A.; Borodeanu, C.

1995-01-01

The system for environmental radioactivity measurements with automatic data transmission represents a better solution for nuclear safety assurance. The 'intelligent probe' will be of real use for surveying the environmental radioactivity. The probes work independently. They measure the dose rate and store the data in their internal memory. Many such probes can be spread all over a large area. They are able to measure dose rate from the background level up to high catastrophic levels. A central computer 'asks' periodically the probes to send their stored data. This computer stores the data from many probes over a long time. It can show in 'windows' manner the dose rate from any probe (either in a numerical or graphical way), the position on a map of every probe and the corresponding results of the measurements. In can alert, if an alarm threshold is crossed or it can print on a printer the data for any single probe. (author)

An overview of human biomonitoring of environmental chemicals in the Canadian Health Measures Survey: 2007-2019.

Science.gov (United States)

Haines, Douglas A; Saravanabhavan, Gurusankar; Werry, Kate; Khoury, Cheryl

2017-03-01

Human biomonitoring (HBM) is used to indicate and quantify exposure by measuring environmental chemicals, their metabolites or reaction products in biological specimens. The biomonitoring component of the Canadian Health Measures Survey (CHMS) is the most comprehensive initiative providing general population HBM data in Canada. The CHMS is an ongoing cross-sectional direct measures survey implemented in 2-year cycles. It provides nationally-representative data on health, nutritional status, environmental exposures, and related risks and protective characteristics. The survey follows a robust planning, design and sampling protocol as well as a comprehensive quality assurance and quality control regime implemented for all aspect of the survey to ensure the validity of the HBM results. HBM blood and urine data are available for CHMS cycles 1 (2007-2009), 2 (2009-2011) and 3 (2012-2013). Field collection has been completed for cycle 4 (2014-2015), with cycle 5 (2016-2017) in progress and cycle 6 planning (2018-2019) being finalized. Biomonitoring results for 279 chemicals are expected over the six cycles of the CHMS (220 in individual blood, urine or hair samples, and 59 in pooled serum samples). The chemicals include metals and trace elements, polychlorinated biphenyls (PCBs), organochlorines, flame retardants, perfluoroalkyl substances, volatile organic compounds (VOCs) and metabolites, environmental phenols, triclocarban, acrylamide, pesticides (e.g., triazines, carbamates, organophosphates, phenoxy, pyrethroids) and/or their metabolites, chlorophenols, polycyclic aromatic hydrocarbon (PAH) metabolites, phthalates and alternate plasticizer metabolites, and tobacco biomarkers. Approximately one half of the chemicals measured in individual blood and urine samples over the first three cycles were detected in more than 60% of samples. CHMS biomonitoring data have been used to establish baseline HBM concentrations in Canadians; inform public health, regulatory risk

Assessment of the Capability of the NGDS Prototype to Replace the JBAIDS for Environmental Sample Analysis

Science.gov (United States)

2016-11-01

Diagnostic System (JBAIDS) for environmental sample analysis. JUPITR ATD and USAF members analyzed environmental samples using the FilmArray...requires 60+ min for sample preparation, whereas the FilmArray system (right) uses highly multiplexed assay pouches that require ᝺ min for sample...supported the evaluation of the BDCoE by analyzing spiked DFU samples using the Joint Biological Agent Identification and Diagnostic System (JBAIDS) and the

Intelligent sampling for the measurement of structured surfaces

International Nuclear Information System (INIS)

Wang, J; Jiang, X; Blunt, L A; Scott, P J; Leach, R K

2012-01-01

Uniform sampling in metrology has known drawbacks such as coherent spectral aliasing and a lack of efficiency in terms of measuring time and data storage. The requirement for intelligent sampling strategies has been outlined over recent years, particularly where the measurement of structured surfaces is concerned. Most of the present research on intelligent sampling has focused on dimensional metrology using coordinate-measuring machines with little reported on the area of surface metrology. In the research reported here, potential intelligent sampling strategies for surface topography measurement of structured surfaces are investigated by using numerical simulation and experimental verification. The methods include the jittered uniform method, low-discrepancy pattern sampling and several adaptive methods which originate from computer graphics, coordinate metrology and previous research by the authors. By combining the use of advanced reconstruction methods and feature-based characterization techniques, the measurement performance of the sampling methods is studied using case studies. The advantages, stability and feasibility of these techniques for practical measurements are discussed. (paper)

Nontuberculous Mycobacteria Isolation from Clinical and Environmental Samples in Iran: Twenty Years of Surveillance

Directory of Open Access Journals (Sweden)

Ali Akbar Velayati

2015-01-01

Full Text Available Nontuberculous mycobacteria (NTM are opportunistic pathogens that are widely distributed in the environment. There is a lack of data on species distribution of these organisms from Iran. This study consists of a review of NTM articles published in Iran between the years 1992 and 2014. In this review, 20 articles and 14 case reports were identified. Among the 20 articles, 13 (65% studies focused on NTM isolates from clinical specimens, 6 (30% studies examined NTM isolates from environmental samples, and one (5% article included both clinical and environmental isolates. M. fortuitum (229/997; 23% was recorded as the most prevalent and rapid growing mycobacteria (RGM species in both clinical (28% and environmental (19% isolated samples (P < 0.05. Among slow growing mycobacteria (SGM, M. simiae (103/494; 21% demonstrated a higher frequency in clinical samples whereas in environmental samples it was M. flavescens (44/503; 9%. These data represent information from 14 provinces out of 31 provinces of Iran. No information is available in current published data on clinical or environmental NTM from the remaining 17 provinces in Iran. These results emphasize the potential importance of NTM as well as the underestimation of NTM frequency in Iran. NTM is an important clinical problem associated with significant morbidity and mortality in Iran. Continued research is needed from both clinical and environmental sources to help clinicians and researchers better understand and address NTM treatment and prevention.

Nontuberculous Mycobacteria Isolation from Clinical and Environmental Samples in Iran: Twenty Years of Surveillance.

Science.gov (United States)

Velayati, Ali Akbar; Farnia, Parissa; Mozafari, Mohadese; Mirsaeidi, Mehdi

2015-01-01

Nontuberculous mycobacteria (NTM) are opportunistic pathogens that are widely distributed in the environment. There is a lack of data on species distribution of these organisms from Iran. This study consists of a review of NTM articles published in Iran between the years 1992 and 2014. In this review, 20 articles and 14 case reports were identified. Among the 20 articles, 13 (65%) studies focused on NTM isolates from clinical specimens, 6 (30%) studies examined NTM isolates from environmental samples, and one (5%) article included both clinical and environmental isolates. M. fortuitum (229/997; 23%) was recorded as the most prevalent and rapid growing mycobacteria (RGM) species in both clinical (28%) and environmental (19%) isolated samples (P < 0.05). Among slow growing mycobacteria (SGM), M. simiae (103/494; 21%) demonstrated a higher frequency in clinical samples whereas in environmental samples it was M. flavescens (44/503; 9%). These data represent information from 14 provinces out of 31 provinces of Iran. No information is available in current published data on clinical or environmental NTM from the remaining 17 provinces in Iran. These results emphasize the potential importance of NTM as well as the underestimation of NTM frequency in Iran. NTM is an important clinical problem associated with significant morbidity and mortality in Iran. Continued research is needed from both clinical and environmental sources to help clinicians and researchers better understand and address NTM treatment and prevention.

Results of environmental radio hygienic measurements in Hungary in 2002

International Nuclear Information System (INIS)

Edit Bokori; Andor Kerekes; Judit Guczi; Capote-Cuellar Antonio; Ibolya Maschek; Gyula Szabo; Agota Ugron

2004-01-01

The laboratories of the Radiological Monitoring and Data Acquisition Network act within the organizational frame of the National Public Health and Medical Officers Service (NPHMOS). The tasks of the network are defined by the duties of Ministry of Health, Social and Family Affairs in the field of environmental radiation protection and radiation hygiene under normal situation and radiological emergency, as well. The monitoring program includes the measurements of samples and radionuclides necessary for estimation of the radiation burden of population. On the basis of measurements and dose assessment it can be stated that the effective dose of the Hungarian population from man-made sources (3.6 μSv x y -1 ) is almost three orders of magnitude lower than the dose from natural radiation sources. (author)

Measurement of strontium-89 and strontium-90 in environmental waters. A tentative reference method

International Nuclear Information System (INIS)

1976-03-01

A tentative reference method for the measurement of 89 Sr and 90 Sr in environmental waters is described. Samples of environmental water sources are collected, preserved with acid-strontium carrier, and analyzed for 89 Sr and/or 90 Sr. The isotopes are separated from the sample water by precipitating with stable strontium carrier as carbonate. The strontium carbonate is dissolved, 90 Sr separated, the strontium reprecipitated as carbonate, filtered, and counted for the combined 89 Sr and 90 Sr activity. The 90 y is allowed to grow in from the 90 y activity; the strontium carbonate is redissolved; the 90 y is separated, precipitated, and counted for the 90 Sr determination. The 89 Sr activity is then determined by difference of the total 89 Sr and 90 y and the separate 90 Sr activities. Recoveries are determined from the added and found (recovered) strontium carrier. Counting efficiencies are determined with prepared standard reference samples. Results are reported in pCi/liter

Environmental radiation monitoring around the nuclear facilities

International Nuclear Information System (INIS)

Lee, H.D.; Lee, Y.B.; Lee, W.Y.; Park, D.W.; Chung, B.G.

1980-01-01

For the KAERI site, various environmental samples were collected three times a month, and the natural environmental radiation levels were also measured at each sampling point. Measurements for gross alpha and beta radioactivities of the samples were routinely measured for all samples. Strontium-90 concentrations were also analysed for the fallout and air samples collected daily basis on the roof of the main building. Accumulated exposure including the possibility of determination of low level environmental radiation field by employing thermoluminescent dosimeter, CaSO 4 : Dsub(y)-0.4 teflon disc type, at 6 posts in on-site of the KAERI. As for Kori site, at 19 points of ON, OFF-site, and at the same time the environmental radiation exposure rate at each sampling point were measured. Several environmental samples such as surface soil, pine needles, water samples, milk sample and pasture samples were collected and analysed on a quarterly basis. As a result of the survey it can be said that no significant release of radiation to the environment due to the operations of nuclear facilities including research reactor at the KAERI and power reactor at the Kori has been found during the period of the survey and monitoring. (author)

Environmental and emergency response capabilities of Los Alamos Scientific Laboratory's radiological air sampling program

International Nuclear Information System (INIS)

Gunderson, T.C.

1980-05-01

Environmental and emergency response radiological air sampling capabilities of the Environmental Surveillance Group at Los Alamos Scientific Laboratory are described. The air sampling program provides a supplementary check on the adequacy of containment and effluent controls, determines compliance with applicable protection guides and standards, and assesses potential environmental impacts on site environs. It also allows evaluation of potential individual and total population doses from airborne radionuclides that may be inhaled or serve as a source of external radiation. The environmental program is sufficient in scope to detect fluctuations and long-term trends in atmospheric levels of radioactivity originating onsite. The emergency response capabilities are designed to respond to both onsite unplanned releases and atmospheric nuclear tests

Environmental Measurements Laboratory, annual report 1995

Energy Technology Data Exchange (ETDEWEB)

Krey, P.W.; Heit, M. [eds.

1996-07-01

This report summarizes the activities of the Environmental Measurements Laboratory (EML) for the calendar year 1995 and serves as an annual report to the Director of the Office of Energy Research (ER), the Associate Director and staff of the Office of Health and Environmental Research (OHER), the Manager and staff of the Chicago Operations Office, and our colleagues. Emphasized are the progress and accomplishments of the year, rather than future plans or expectations. The technical summaries are grouped according to the following seven research program areas: (1) Environmental Radiation and Radioactivity; (2) Radiation Transport and Dosimetry; (3) Environmental Radon, Thoron, and Related Aerosols; (4) Atmospheric and Surface Pollutant Studies Related to Global Climate Change; (5) Atmospheric Chemistry; and (6) Metrology, Consultation, and Emergency Response Environmental Management The mission of EML is to address important scientific questions concerning human health and environmental impacts. Through its multidisciplinary staff, EML conducts experimental and theoretical research on radioactive and other energy-related pollutants and provides DOE and other federal agencies with the in-house capability to respond effectively and efficiently with regard to quality assurance activities, environmental issues, and related national security issues.

Environmental Measurements Laboratory, annual report 1995

International Nuclear Information System (INIS)

Krey, P.W.; Heit, M.

1996-07-01

This report summarizes the activities of the Environmental Measurements Laboratory (EML) for the calendar year 1995 and serves as an annual report to the Director of the Office of Energy Research (ER), the Associate Director and staff of the Office of Health and Environmental Research (OHER), the Manager and staff of the Chicago Operations Office, and our colleagues. Emphasized are the progress and accomplishments of the year, rather than future plans or expectations. The technical summaries are grouped according to the following seven research program areas: (1) Environmental Radiation and Radioactivity; (2) Radiation Transport and Dosimetry; (3) Environmental Radon, Thoron, and Related Aerosols; (4) Atmospheric and Surface Pollutant Studies Related to Global Climate Change; (5) Atmospheric Chemistry; and (6) Metrology, Consultation, and Emergency Response Environmental Management The mission of EML is to address important scientific questions concerning human health and environmental impacts. Through its multidisciplinary staff, EML conducts experimental and theoretical research on radioactive and other energy-related pollutants and provides DOE and other federal agencies with the in-house capability to respond effectively and efficiently with regard to quality assurance activities, environmental issues, and related national security issues

Automated image analysis for quantitative fluorescence in situ hybridization with environmental samples.

Science.gov (United States)

Zhou, Zhi; Pons, Marie Noëlle; Raskin, Lutgarde; Zilles, Julie L

2007-05-01

When fluorescence in situ hybridization (FISH) analyses are performed with complex environmental samples, difficulties related to the presence of microbial cell aggregates and nonuniform background fluorescence are often encountered. The objective of this study was to develop a robust and automated quantitative FISH method for complex environmental samples, such as manure and soil. The method and duration of sample dispersion were optimized to reduce the interference of cell aggregates. An automated image analysis program that detects cells from 4',6'-diamidino-2-phenylindole (DAPI) micrographs and extracts the maximum and mean fluorescence intensities for each cell from corresponding FISH images was developed with the software Visilog. Intensity thresholds were not consistent even for duplicate analyses, so alternative ways of classifying signals were investigated. In the resulting method, the intensity data were divided into clusters using fuzzy c-means clustering, and the resulting clusters were classified as target (positive) or nontarget (negative). A manual quality control confirmed this classification. With this method, 50.4, 72.1, and 64.9% of the cells in two swine manure samples and one soil sample, respectively, were positive as determined with a 16S rRNA-targeted bacterial probe (S-D-Bact-0338-a-A-18). Manual counting resulted in corresponding values of 52.3, 70.6, and 61.5%, respectively. In two swine manure samples and one soil sample 21.6, 12.3, and 2.5% of the cells were positive with an archaeal probe (S-D-Arch-0915-a-A-20), respectively. Manual counting resulted in corresponding values of 22.4, 14.0, and 2.9%, respectively. This automated method should facilitate quantitative analysis of FISH images for a variety of complex environmental samples.

Determination of 129I/127I isotope ratios in liquid solutions and environmental soil samples by ICP-MS with hexapole collision cell

OpenAIRE

Izmer, A. V.; Boulyga, S. F.; Becker, J. S.

2003-01-01

The determination of I-129 in environmental samples at ultratrace levels is very difficult by ICP-MS due to a high noise caused by Xe impurities in argon plasma gas (interference of Xe-129(+)), possible (IH2+)-I-127 interference and an insufficient abundance ratio sensitivity of the ICP mass spectrometer for I-129/I-127 isotope ratio measurement. A sensitive, powerful and fast analytical technique for iodine isotope ratio measurements in aqueous solutions and contaminated soil samples directl...

Evaluation of environmental sampling methods for detection of Salmonella enterica in a large animal veterinary hospital.

Science.gov (United States)

Goeman, Valerie R; Tinkler, Stacy H; Hammac, G Kenitra; Ruple, Audrey

2018-04-01

Environmental surveillance for Salmonella enterica can be used for early detection of contamination; thus routine sampling is an integral component of infection control programs in hospital environments. At the Purdue University Veterinary Teaching Hospital (PUVTH), the technique regularly employed in the large animal hospital for sample collection uses sterile gauze sponges for environmental sampling, which has proven labor-intensive and time-consuming. Alternative sampling methods use Swiffer brand electrostatic wipes for environmental sample collection, which are reportedly effective and efficient. It was hypothesized that use of Swiffer wipes for sample collection would be more efficient and less costly than the use of gauze sponges. A head-to-head comparison between the 2 sampling methods was conducted in the PUVTH large animal hospital and relative agreement, cost-effectiveness, and sampling efficiency were compared. There was fair agreement in culture results between the 2 sampling methods, but Swiffer wipes required less time and less physical effort to collect samples and were more cost-effective.

The Revised Perceived Environmental Control Measure: A Review and Analysis.

Science.gov (United States)

Smith-Sebasto, N. J.

1992-01-01

A study reveals the need for extensive refinement of the Revised Perceived Environmental Control Measure purported in the past to be a reliable and valid instrument to measure the relationship between the psychological construct, "locus of control," and environmental action or environmentally responsible behavior. (MCO)

The French National Network for the Measurement of Environmental Radioactivity

International Nuclear Information System (INIS)

Jaunet, P.

2010-01-01

After Chernobyl accident in 1986, the government began to implement mechanisms to ensure the quality of measurements of environmental radioactivity and to assure the transparency of information on environmental radioactivity monitoring results. Within this context, the French National Network for the Measurement of Environmental Radioactivity (RNM), is created in 2002 under the Public Health Code. This network is developed under the auspices of ASN in collaboration with IRSN and in partnership with government departments, major nuclear licensees, health agencies and environmental protection associations. In order to centralize information on environmental radioactivity and to provide access to measurement results, a single database that includes an the results of measurements of radioactivity in the environment on the national territory is build and a new web-site www.mesure-radioactivite.fr is launched. It provides quick and easy access to this database. The quality of measurements is performed by a laboratory system through an ASN decision. Novel initiative in Europe, the French National Network for the Measurement of Environmental Radioactivity web-site gives the user keys to understand the measurement results on the radiological state of the environment. The site will be improved over the time taking into account the feedback of the users. (author)

Rapid determination of strontium-90 in environmental samples by single Cerenkov counting using two different colour quench curves

Energy Technology Data Exchange (ETDEWEB)

Torres, J.M.; Garcia, J.F.; Llaurado, M.; Rauret, G. [Barcelona Univ. (Spain). Dept. de Quimica Analitica

1996-11-01

The validation of the Cerenkov radiation measurement of {sup 90}Y to determine the activity concentration of {sup 90}Sr in environmental samples is described. Liquid-liquid extraction with di-2-ethyhexylphosphoric acid in toluene was used to separate {sup 90}Y from {sup 90}Sr. Optimum conditions for Cerenkov counting (low-level counting option, counting windows, mass of solution to be measured) were established. The need for a counting efficiency correction by using a colour quench curve is stated to be essential, otherwise a significant error may occur. Two different colour quench curves (counting efficiency versus the channel ratio or spectral index parameter) were used and the results were compared. The method was applied to 12 environmental matrices: sea-water, algae, carobs, milk, almonds, hake, honey, shellfish, lamb meat, sardine, pork meat and shore sand. No significant differences were observed on using either of the two colour quench curves for any of these environmental matrices. In order to validate the proposed method, a certified soil reference material (CRM IAEA-375) was used, together with participation in an interlaboratory exercise to determine {sup 90}Sr in a natural water sample. Again, efficiency correction was performed by using either of the two colour quench curves and in both instances the calculated {sup 90}Sr activity concentration was in good agreement with the known values. (Author).

A Procedure for the Sequential Determination of Radionuclides in Environmental Samples. Liquid Scintillation Counting and Alpha Spectrometry for 90Sr, 241Am and Pu Radioisotopes

International Nuclear Information System (INIS)

2014-01-01

Since 2004, IAEA activities related to the terrestrial environment have aimed at the development of a set of procedures to determine radionuclides in environmental samples. Reliable, comparable and ‘fit for purpose’ results are an essential requirement for any decision based on analytical measurements. For the analyst, tested and validated analytical procedures are extremely important tools for the production of analytical data. For maximum utility, such procedures should be comprehensive, clearly formulated and readily available for reference to both the analyst and the customer. This publication describes a combined procedure for the sequential determination of 90 Sr, 241 Am and Pu radioisotopes in environmental samples. The method is based on the chemical separation of strontium, americium and plutonium using ion exchange chromatography, extraction chromatography and precipitation followed by alpha spectrometric and liquid scintillation counting detection. The method was tested and validated in terms of repeatability and trueness in accordance with International Organization for Standardization (ISO) guidelines using reference materials and proficiency test samples. Reproducibility tests were performed later at the IAEA Terrestrial Environment Laboratory. The calculations of the massic activity, uncertainty budget, decision threshold and detection limit are also described in this publication. The procedure is introduced for the determination of 90 Sr, 241 Am and Pu radioisotopes in environmental samples such as soil, sediment, air filter and vegetation samples. It is expected to be of general use to a wide range of laboratories, including the Analytical Laboratories for the Measurement of Environmental Radioactivity (ALMERA) network for routine environmental monitoring purposes

Measurement of neutron activation in concrete samples

International Nuclear Information System (INIS)

Zagar, T.; Ravnik, M.

2000-01-01

The results of activation studies of ordinary and barytes concrete samples relevant for research reactor decommissioning are given. Five important long-lived radioactive isotopes ( 54 Mn, 60 Co, 65 Zn, 133 Ba, and 152 Eu) were identified from the gamma-ray spectra measured in the irradiated concrete samples. Activation of these samples was also calculated using ORIGEN2 code. Comparison of calculated and measured results is given. (author)

A data acquisition system for indentification of 90Sr/ 90Y in environmental samples

International Nuclear Information System (INIS)

Medin, G.; Brajnik, D.; Starcic, M.; Stanovnik, A.

1996-01-01

Often, in the stage of research and development of new techniques for detection of ionizing radiation, elaborate electronic systems are required. In this paper, we describe the relatively complex detector and electronic system used for a relatively simple but nevertheless demanding measurement of the beta emitting radionuclides 90 Sr/ 90 Y in environmental samples. The detection limit of 1 Bq in a thin, disc-shaped sample, was obtained by careful elimination of background. Contribution of other radionuclides in the sample, were eliminated or at least considerably reduced by using a silica aerogel as Cherenkov radiator and thin multiwire chamber in coincidence. Cosmic ray signals were reduced by large scintillation counters in anticoincidence. Finally, persisting RF pick-up signals were eliminated by using the signal from a wire antenna and identical MWPC preamplifier and discriminator for a veto to the master coincidence. For each accepted event, both timing and pulse height information was recorded with a personal computer

Moving your laboratories to the field – Advantages and limitations of the use of field portable instruments in environmental sample analysis

Energy Technology Data Exchange (ETDEWEB)

Gałuszka, Agnieszka, E-mail: Agnieszka.Galuszka@ujk.edu.pl [Geochemistry and the Environment Division, Institute of Chemistry, Jan Kochanowski University, 15G Świętokrzyska St., 25-406 Kielce (Poland); Migaszewski, Zdzisław M. [Geochemistry and the Environment Division, Institute of Chemistry, Jan Kochanowski University, 15G Świętokrzyska St., 25-406 Kielce (Poland); Namieśnik, Jacek [Department of Analytical Chemistry, Chemical Faculty, Gdańsk University of Technology (GUT), 11/12 G. Narutowicz St., 80-233 Gdańsk (Poland)

2015-07-15

The recent rapid progress in technology of field portable instruments has increased their applications in environmental sample analysis. These instruments offer a possibility of cost-effective, non-destructive, real-time, direct, on-site measurements of a wide range of both inorganic and organic analytes in gaseous, liquid and solid samples. Some of them do not require the use of reagents and do not produce any analytical waste. All these features contribute to the greenness of field portable techniques. Several stationary analytical instruments have their portable versions. The most popular ones include: gas chromatographs with different detectors (mass spectrometer (MS), flame ionization detector, photoionization detector), ultraviolet–visible and near-infrared spectrophotometers, X-ray fluorescence spectrometers, ion mobility spectrometers, electronic noses and electronic tongues. The use of portable instruments in environmental sample analysis gives a possibility of on-site screening and a subsequent selection of samples for routine laboratory analyses. They are also very useful in situations that require an emergency response and for process monitoring applications. However, quantification of results is still problematic in many cases. The other disadvantages include: higher detection limits and lower sensitivity than these obtained in laboratory conditions, a strong influence of environmental factors on the instrument performance and a high possibility of sample contamination in the field. This paper reviews recent applications of field portable instruments in environmental sample analysis and discusses their analytical capabilities. - Highlights: • Field portable instruments are widely used in environmental sample analysis. • Field portable instruments are indispensable for analysis in emergency response. • Miniaturization of field portable instruments reduces resource consumption. • In situ analysis is in agreement with green analytical chemistry

Moving your laboratories to the field – Advantages and limitations of the use of field portable instruments in environmental sample analysis

International Nuclear Information System (INIS)

Gałuszka, Agnieszka; Migaszewski, Zdzisław M.; Namieśnik, Jacek

2015-01-01

The recent rapid progress in technology of field portable instruments has increased their applications in environmental sample analysis. These instruments offer a possibility of cost-effective, non-destructive, real-time, direct, on-site measurements of a wide range of both inorganic and organic analytes in gaseous, liquid and solid samples. Some of them do not require the use of reagents and do not produce any analytical waste. All these features contribute to the greenness of field portable techniques. Several stationary analytical instruments have their portable versions. The most popular ones include: gas chromatographs with different detectors (mass spectrometer (MS), flame ionization detector, photoionization detector), ultraviolet–visible and near-infrared spectrophotometers, X-ray fluorescence spectrometers, ion mobility spectrometers, electronic noses and electronic tongues. The use of portable instruments in environmental sample analysis gives a possibility of on-site screening and a subsequent selection of samples for routine laboratory analyses. They are also very useful in situations that require an emergency response and for process monitoring applications. However, quantification of results is still problematic in many cases. The other disadvantages include: higher detection limits and lower sensitivity than these obtained in laboratory conditions, a strong influence of environmental factors on the instrument performance and a high possibility of sample contamination in the field. This paper reviews recent applications of field portable instruments in environmental sample analysis and discusses their analytical capabilities. - Highlights: • Field portable instruments are widely used in environmental sample analysis. • Field portable instruments are indispensable for analysis in emergency response. • Miniaturization of field portable instruments reduces resource consumption. • In situ analysis is in agreement with green analytical chemistry

Environmental radiation monitoring from the decommission of TRIGA

Energy Technology Data Exchange (ETDEWEB)

Choi, Geun Sik; Lee, Chang Woo

2000-03-01

Environmental radiation monitoring was carried out with measurement of environmental radiation and environmental radioactivity analysis around TRIGA Research Reactor. The results of environmental radiation monitoring around TRIGA Research Reactor are the follows: The average level of environmental radiation measured by potable ERM and accumulated radiation dose by TLD was almost same level compared with thepast years. Gross {beta} radioactivity in environmental samples showed a environmental level. {gamma}-radionuclides in water samples were not detected. but only radionuclide K-40, which is natural radionuclide, was detected in the all samples and Cs-137 was detected in the surface soil and discharge sediment. (author)

Environmental radioactivity measurements in north-western Greece following the Fukushima nuclear accident

International Nuclear Information System (INIS)

Ioannides, K.; Stamoulis, K.; Papachristodoulou, C.

2013-01-01

The impact of the Fukushima nuclear accident in north–western Greece was assessed through an environmental monitoring programme activated by the Nuclear Physics Laboratory of the University of Ioannina. Measurements of 131 I were carried out in atmospheric particulate, ovine milk and grass samples. In daily aerosol samplings, radioiodine was first detected on March 25-26, 2011 and reached maximum levels, up to 294 μBq m -3 , between April 2 and April 4, 2011. In ovine milk samples, 131 I concentrations ranged from 2.0 to 2.7 Bq L -1 between April 2 and April 6, 2011, while an average activity of 2.7 Bq kg -1 was measured in grass samples on April 4, 2011. The 134,137 Cs isotopes were below detection limits in all samples and could only be determined in the air, by analysis of multiple daily filters. A maximum average activity concentration of 137 Cs amounting to 24 μBq m -3 was measured during the period from April 5 to April 9, 2011, with the 134 Cs/ 137 Cs activity ratio being close to unity. Activity concentrations were consistent with measurements conducted in other parts of the country and were well below those reported in May 1986 after the Chernobyl accident. The committed effective dose to the whole body and to the thyroid gland from inhalation of 131 I was estimated for the adult and infant population and was found to be of no concern for the public health. (author)

Robust weak measurements on finite samples

International Nuclear Information System (INIS)

Tollaksen, Jeff

2007-01-01

A new weak measurement procedure is introduced for finite samples which yields accurate weak values that are outside the range of eigenvalues and which do not require an exponentially rare ensemble. This procedure provides a unique advantage in the amplification of small nonrandom signals by minimizing uncertainties in determining the weak value and by minimizing sample size. This procedure can also extend the strength of the coupling between the system and measuring device to a new regime

Environmental radioactivity. Measurement and monitoring

International Nuclear Information System (INIS)

2009-11-01

The contribution on environmental radioactivity covers the following issues: natural and artificial radioactivity; continuous monitoring of radioactivity; monitoring authorities and measurement; radioactivity in the living environment; radioactivity in food and feeding stuff; radioactivity of game meat and wild-growing mushrooms; radioactivity in mines; radioactivity in the research center Rossendorf.

Self-attenuation correction in the environmental sample gamma spectrometry; Correcao de auto-absorcao na espectrometria gama de amostras ambientais

Energy Technology Data Exchange (ETDEWEB)

Venturini, Luzia; Nisti, Marcelo B. [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)

1997-10-01

Self-attenuation corrections were calculated for gamma ray spectrometry of environmental samples with densities from 0.42 g/ml up to 1.59 g/ml, measured in Marinelli beakers and polyethylene flasks. These corrections are to be used when the counting efficiency is calculated for water measured in the same geometry. The model of Debertin for Marinelli beaker, numerical integration and experimental linear attenuation coefficients were used. (author). 3 refs., 4 figs., 6 tabs.

Stability of metal ions in aqueous environmental samples

International Nuclear Information System (INIS)

Rattonetti, A.

1976-01-01

The time lapse between the collection of aqueous environmental samples and the analysis affects the original ionic concentration. Studies have proven the nonionic species in a water sample have more of an effect on the veracity of an analysis than the ''container wall'' effect, and that adjustment to a pH of 2 at sample collection time is a ''Pyrrhic victory.'' Lead, for example, will commonly increase an order of magnitude when unfiltered samples are adjusted to a pH of 2 upon collection. This effect is greatest when elemental ions are present in the ng ml -1 range and lessens as the original ionic concentration increases. Data are presented that behooves filtration of stream water and rainwater samples prior to any acidification step. The need to acidify the resulting filtrate is also discussed. Lithium, sodium, potassium, cesium, magnesium, calcium, strontium, manganese, iron, copper, silver, zinc, cadmium, aluminum, indium, and lead are examined. The insoluble phase retained on the filter can be digested with acid and also analyzed. The separate analysis of the filtrate and filter will give a true representation of the occurrence of these metals in nature. Flame and flameless atomic aborption and emission are used to perform the trace analyses

Best-Matched Internal Standard Normalization in Liquid Chromatography-Mass Spectrometry Metabolomics Applied to Environmental Samples.

Science.gov (United States)

Boysen, Angela K; Heal, Katherine R; Carlson, Laura T; Ingalls, Anitra E

2018-01-16

The goal of metabolomics is to measure the entire range of small organic molecules in biological samples. In liquid chromatography-mass spectrometry-based metabolomics, formidable analytical challenges remain in removing the nonbiological factors that affect chromatographic peak areas. These factors include sample matrix-induced ion suppression, chromatographic quality, and analytical drift. The combination of these factors is referred to as obscuring variation. Some metabolomics samples can exhibit intense obscuring variation due to matrix-induced ion suppression, rendering large amounts of data unreliable and difficult to interpret. Existing normalization techniques have limited applicability to these sample types. Here we present a data normalization method to minimize the effects of obscuring variation. We normalize peak areas using a batch-specific normalization process, which matches measured metabolites with isotope-labeled internal standards that behave similarly during the analysis. This method, called best-matched internal standard (B-MIS) normalization, can be applied to targeted or untargeted metabolomics data sets and yields relative concentrations. We evaluate and demonstrate the utility of B-MIS normalization using marine environmental samples and laboratory grown cultures of phytoplankton. In untargeted analyses, B-MIS normalization allowed for inclusion of mass features in downstream analyses that would have been considered unreliable without normalization due to obscuring variation. B-MIS normalization for targeted or untargeted metabolomics is freely available at https://github.com/IngallsLabUW/B-MIS-normalization .

Rapid filtration separation-based sample preparation method for Bacillus spores in powdery and environmental matrices.

Science.gov (United States)

Isabel, Sandra; Boissinot, Maurice; Charlebois, Isabelle; Fauvel, Chantal M; Shi, Lu-E; Lévesque, Julie-Christine; Paquin, Amélie T; Bastien, Martine; Stewart, Gale; Leblanc, Eric; Sato, Sachiko; Bergeron, Michel G

2012-03-01

Authorities frequently need to analyze suspicious powders and other samples for biothreat agents in order to assess environmental safety. Numerous nucleic acid detection technologies have been developed to detect and identify biowarfare agents in a timely fashion. The extraction of microbial nucleic acids from a wide variety of powdery and environmental samples to obtain a quality level adequate for these technologies still remains a technical challenge. We aimed to develop a rapid and versatile method of separating bacteria from these samples and then extracting their microbial DNA. Bacillus atrophaeus subsp. globigii was used as a simulant of Bacillus anthracis. We studied the effects of a broad variety of powdery and environmental samples on PCR detection and the steps required to alleviate their interference. With a benchmark DNA extraction procedure, 17 of the 23 samples investigated interfered with bacterial lysis and/or PCR-based detection. Therefore, we developed the dual-filter method for applied recovery of microbial particles from environmental and powdery samples (DARE). The DARE procedure allows the separation of bacteria from contaminating matrices that interfere with PCR detection. This procedure required only 2 min, while the DNA extraction process lasted 7 min, for a total of sample preparation procedure allowed the recovery of cleaned bacterial spores and relieved detection interference caused by a wide variety of samples. Our procedure was easily completed in a laboratory facility and is amenable to field application and automation.

Determination of 129I in environmental samples by AMS and NAA using an anion exchange resin disk

Science.gov (United States)

Suzuki, Takashi; Banba, Shigeru; Kitamura, Toshikatsu; Kabuto, Shoji; Isogai, Keisuke; Amano, Hikaru

2007-06-01

We have developed a new extraction method for the measurement of 129I by accelerator mass spectrometry (AMS) utilizing an anion exchange resin disk. In comparison to traditional methods such as solvent extraction and ion exchange, this method provides for simple and quick sample handling. This extraction method was tested on soil, seaweed and milk samples, but because of disk clogging, the milk samples and some of the seaweed could not be applied successfully. Using this new extraction method to prepare samples for AMS analysis produced isotope ratios of iodine in good agreement with neutron activation analysis (NAA). The disk extraction method which take half an hour is faster than previous techniques, such as solvent extraction or ion exchange which take a few hours. The combination of the disk method and the AMS measurement is a powerful tool for the determination of 129I. Furthermore, these data will be available for the environmental monitoring before and during the operation of a new nuclear fuel reprocessing plant in Japan.

Determination of 129I in environmental samples by AMS and NAA using an anion exchange resin disk

International Nuclear Information System (INIS)

Suzuki, Takashi; Banba, Shigeru; Kitamura, Toshikatsu; Kabuto, Shoji; Isogai, Keisuke; Amano, Hikaru

2007-01-01

We have developed a new extraction method for the measurement of 129 I by accelerator mass spectrometry (AMS) utilizing an anion exchange resin disk. In comparison to traditional methods such as solvent extraction and ion exchange, this method provides for simple and quick sample handling. This extraction method was tested on soil, seaweed and milk samples, but because of disk clogging, the milk samples and some of the seaweed could not be applied successfully. Using this new extraction method to prepare samples for AMS analysis produced isotope ratios of iodine in good agreement with neutron activation analysis (NAA). The disk extraction method which take half an hour is faster than previous techniques, such as solvent extraction or ion exchange which take a few hours. The combination of the disk method and the AMS measurement is a powerful tool for the determination of 129 I. Furthermore, these data will be available for the environmental monitoring before and during the operation of a new nuclear fuel reprocessing plant in Japan

Environmental measures for Escuintla No. 3 unit thermal power project

Energy Technology Data Exchange (ETDEWEB)

Quisquinay, Carlos; Fabian Rosales, Alejandro [Instituto Nacional de Electrificacion, (Guatemala)

1997-12-31

The environmental measures in relation to the project implementation was studied with reference to the Japanese Standards and incorporated in the Implementation Program. This report is prepared however, to review the environmental measures for the project in more detail as to the allowable standards and regulations concerning the measures for the environmental pollution. The authors present the environmental conditions around the Escuintla Power Station in Guatemala; the measures for environmental pollution and evaluation; the measures for prevention of air pollution and diffusion calculations (estimation and assessment of environmental impacts) [Espanol] Las medidas ambientales con relacion a la consolidacion del proyecto, se estudiaron con referencia a los Estandares Japoneses e incorporados en el Programa de Consolidacion. Sin embargo, este reporte ha sido preparado para revisar las medidas ambientales para el proyecto mas detalladamente, con relacion a los estandares y reglamentaciones admisibles concernientes a las medidas de contaminacion ambiental. Los autores presentan las condiciones ambientales en los alrededores de la Central Termoelectrica de Escuintla de Guatemala; las medidas para la prevencion de la contaminacion del aire y los calculos de difusion (estimacion y evaluacion del impacto ambiental)

Environmental measures for Escuintla No. 3 unit thermal power project

Energy Technology Data Exchange (ETDEWEB)

Quisquinay, Carlos; Fabian Rosales, Alejandro [Instituto Nacional de Electrificacion, (Guatemala)

1996-12-31

The environmental measures in relation to the project implementation was studied with reference to the Japanese Standards and incorporated in the Implementation Program. This report is prepared however, to review the environmental measures for the project in more detail as to the allowable standards and regulations concerning the measures for the environmental pollution. The authors present the environmental conditions around the Escuintla Power Station in Guatemala; the measures for environmental pollution and evaluation; the measures for prevention of air pollution and diffusion calculations (estimation and assessment of environmental impacts) [Espanol] Las medidas ambientales con relacion a la consolidacion del proyecto, se estudiaron con referencia a los Estandares Japoneses e incorporados en el Programa de Consolidacion. Sin embargo, este reporte ha sido preparado para revisar las medidas ambientales para el proyecto mas detalladamente, con relacion a los estandares y reglamentaciones admisibles concernientes a las medidas de contaminacion ambiental. Los autores presentan las condiciones ambientales en los alrededores de la Central Termoelectrica de Escuintla de Guatemala; las medidas para la prevencion de la contaminacion del aire y los calculos de difusion (estimacion y evaluacion del impacto ambiental)

Radon and radon daughter measurements and methods utilized by EPA's Eastern Environmental Radiation Facility

International Nuclear Information System (INIS)

Phillips, C.R.

1977-01-01

The Eastern Environmental Radiation Facility (EERF), Office of Radiation Programs, has the responsibility for conducting the Environmental Protection Agency's study of the radiological impact of the phosphate industry. Numerous measurements in structures constructed on land reclaimed from phosphate mining showed that working levels in these structures range from 0.001 to 0.9 WL. Sampling is performed by drawing air through a 0.8 micrometer pore size, 25 mm diameter filter at a flow rate of 10 to 15 liters/minute for from 5 to 20 minutes, depending on the daughter levels anticipated. The detection system consists of a ruggedized silicon surface barrier detector (450 mm 2 -100 micrometer depletion) connected through an appropriate pre-amplifier-amplifier to a 1024-channel multichannel analyzer. Other measurement methods are also discussed

Measurement of Iodine-129 concentration in environmental water samples around Fukushima area - Role of river system in the global iodine cycle

Science.gov (United States)

Matsuzaki, Hiroyuki; Tokuyama, Hironori; Miyake, Yasuto; Honda, Maki; Yamagata, Takeyasu; Muramatsu, Yasuyuki

2013-04-01

According to Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident, vast amount of radioactive nuclides including radioactive iodine were spilled out into the environment. There is no question about that detailed observation of distribution of radioactive nuclides and evaluation of the radiation exposure of residents is extremely important. On the other hand, from the view of an elemental dynamics in the environment, this event can be considered as a spike of the radioactive isotope. It is also the case for the iodine. A rare isotope Iodine-129 was widely distributed in a very short time by the FDNPP accident. Iodine-129 directly landing on the soil surface had been trapped in the upper layer of the soil and the depth profile should indicate the migration in and the interaction with the soil. If Iodine-129 was trapped in the woods, it seems to take rather longer time to landing on the ground. Either way, a certain portion of the Iodine-129 should be moving downward and finally washed out by the groundwater or river with a certain rate and transported into the sea. The concentration of Iodine-129 in environmental water samples taken from rivers and ponds are considered to reflect the iodine transportation process by the fluvial system. For the detailed discussion of the role of the fluvial system in the global iodine cycle, Iodine-129 concentration of various water samples collected from Fukushima area was measured by means of Accelerator Mass Spectrometry. The results ranged from 3E06 atoms/L to 3E09 atoms/L. Samples from Abukuma area (South West of FDNPP) showed lower concentration. On the other hand, samples collected from North West part (Iitate village and Minami Soma region) showed higher concentration (more than 1E8 atoms/L). Delayed enhancement of Iodine-129 concentration over a year in river systems surrounded by woods was also observed which is considered to correspond to the delayed release from the woods.

Device for radioactivity measurement of liquid samples

International Nuclear Information System (INIS)

Lamaziere, J.

1983-01-01

The device for low activity gamma measurements comprises an automatic changer for sample transfer from a conveyor to a measuring chamber. The conveyor includes a horizontal table were are regularly distributed sample holders. A lift allows a vertical motion of a plate for the exposition in front of a detector [fr

Isotope Enrichment Detection by Laser Ablation - Laser Absorption Spectrometry: Automated Environmental Sampling and Laser-Based Analysis for HEU Detection

International Nuclear Information System (INIS)

Anheier, Norman C.; Bushaw, Bruce A.

2010-01-01

The global expansion of nuclear power, and consequently the uranium enrichment industry, requires the development of new safeguards technology to mitigate proliferation risks. Current enrichment monitoring instruments exist that provide only yes/no detection of highly enriched uranium (HEU) production. More accurate accountancy measurements are typically restricted to gamma-ray and weight measurements taken in cylinder storage yards. Analysis of environmental and cylinder content samples have much higher effectiveness, but this approach requires onsite sampling, shipping, and time-consuming laboratory analysis and reporting. Given that large modern gaseous centrifuge enrichment plants (GCEPs) can quickly produce a significant quantity (SQ ) of HEU, these limitations in verification suggest the need for more timely detection of potential facility misuse. The Pacific Northwest National Laboratory (PNNL) is developing an unattended safeguards instrument concept, combining continuous aerosol particulate collection with uranium isotope assay, to provide timely analysis of enrichment levels within low enriched uranium facilities. This approach is based on laser vaporization of aerosol particulate samples, followed by wavelength tuned laser diode spectroscopy to characterize the uranium isotopic ratio through subtle differences in atomic absorption wavelengths. Environmental sampling (ES) media from an integrated aerosol collector is introduced into a small, reduced pressure chamber, where a focused pulsed laser vaporizes material from a 10 to 20-(micro)m diameter spot of the surface of the sampling media. The plume of ejected material begins as high-temperature plasma that yields ions and atoms, as well as molecules and molecular ions. We concentrate on the plume of atomic vapor that remains after the plasma has expanded and then cooled by the surrounding cover gas. Tunable diode lasers are directed through this plume and each isotope is detected by monitoring absorbance

210Pb and 210Po determination in environmental samples using liquid scintillation counting and alpha spectrometry

International Nuclear Information System (INIS)

Perez Sanchez, D.; Martin Sanchez, A.; Jurado Vargas, M.

2003-01-01

A simple radiochemical procedure has been developed to determine 210 Pb and 210 Po in environmental samples from the same matrix. Sediment samples are decomposed by leaching with mineral acids or by microwave digestion, while water samples are pre-concentrated. One part of the resulting solution, spiked with 209 Po, is used for 210 Po determination by spontaneous deposition onto nickel disks (a-spectrometry). The other part is assayed for 210 Pb, separating the Pb either by anion-exchange (sediment samples), or by solvent extraction (water samples). The 210 Pb source is finally prepared by precipitation as oxalate and the chemical recovery determined by gravimetry. The 210 Pb activity concentration is determined by liquid scintillation. A standard sediment sample supplied by IAEA and spiked water samples were analysed to check the procedure. The 210 Pb and 210 Po measurements agreed well with the certifications, deviations being less than 10%. The mean recoveries for Pb and Po were (70±12)% and (77±8)% for sediments, and (70±10)% and (81±7)% for waters, respectively. (author)

Design of a radioactive gas sampling system for NESHAP compliance measurements of 41Ar

International Nuclear Information System (INIS)

Newton, G.J.; McDonald, M.J.; Ghanbari, F.; Hoover, M.D.; Barr, E.B.

1994-01-01

United States Department of Energy facilities are required to comply with the U.S. Environmental Protection Agency, National Emission Standard for Hazardous Air Pollutants (NESHAP) 40 CFR, part 61, subpart H. Compliance generally requires confirmatory measurements of emitted radionuclides. Although a number of standard procedures exist for extractive sampling of particle-associated radionuclides, sampling approaches for radioactive gases are less defined. Real-time, flow-through sampling of radioactive gases can be done when concentrations are high compared to interferences from background radiation. Cold traps can be used to collect and concentrate condensible effluents in applications where cryogenic conditions can be established and maintained. Commercially available gas-sampling cylinders can be used to capture grab samples of contaminated air under ambient or compressed conditions, if suitable sampling and control hardware are added to the cylinders. The purpose of the current study was to develop an efficient and compact set of sampling and control hardware for use with commercially available gas-sampling cylinders, and to demonstrate its use in NESHAP compliance testing of 41 Ar at two experimental research reactors

Identification and assay of radionuclides in the environmental samples following Chernobyl reactor accident

International Nuclear Information System (INIS)

Prakash, S.

1987-01-01

In India radioactivity was detected from 2 May 1986 onwards. A variety of samples were assayed for radionuclides in the environmental samples originating from the Chernobyl reactor accident. These are: Cotton swipe samples from aircrafts, air filters, milk, goat thyroids, grass, vegetables and tap waters. The results are presented in the paper

Political measures for promoting environmental technology; Virkemidler for aa fremme miljoeteknologi

Energy Technology Data Exchange (ETDEWEB)

NONE

2006-07-01

Environmental technology can contribute to solving many environmental challenges and to industrial development. Measures to support the development and use of such technologies can be regulatory, economic or administrative, and usually one needs to use a combination of different measures in order to reach both a better environment and industrial development. For industrial development other measures than those administered by environmental authorities will be of importance. The environmental authorities therefore need to acquire knowledge about these measures and the bodies administering them, and develop an operative cooperation with these actors.

Potential Use of Passive Sampling for Environmental Monitoring of Petroleum E&P Operations

Science.gov (United States)

Traditional environmental monitoring relies on water or soil samples being taken at various time increments and sent to offsite laboratories for analysis. Reliance on grab samples generally captures limited “snapshots” of environmental contaminant concentrations, is time intensive, costly, and generates residual waste from excess sample and/or reagents used in the analysis procedures. As an alternative, we are evaluating swellable organosilica sorbents to create passive sampling systems for monitoring applications. Previous work has focused on absorption and detection of fuels, chlorinated solvents, endocrine disruptors, explosives, pesticides, fluorinated chemicals, and metals including Ba, Sr, Hg, Pb, Fe, Cu, and Zn. The advantages of swellable organosilica are that the material cancapture target compounds for an extended periods of time, does not absorb natural organic matter, and resists biofilm formation since the sorbent possesses an animated surface morphology.

Green Aspects of Techniques for the Determination of Currently Used Pesticides in Environmental Samples

OpenAIRE

Maciej Tankiewicz; Jacek Namieśnik; Jolanta Stocka; Marek Biziuk

2011-01-01

Pesticides are among the most dangerous environmental pollutants because of their stability, mobility and long-term effects on living organisms. Their presence in the environment is a particular danger. It is therefore crucial to monitor pesticide residues using all available analytical methods. The analysis of environmental samples for the presence of pesticides is very difficult: the processes involved in sample preparation are labor-intensive and time-consuming. To date, it has been standa...

Improved sample preparation method for environmental plutonium analysis by ICP-SFMS and alpha-spectrometry

International Nuclear Information System (INIS)

Varga, Z.; Stefanka, Z.; Suranyi, G.; Vajda, N.

2007-01-01

A rapid and simple sample preparation method for plutonium determination in environmental samples by inductively coupled plasma sector field mass spectrometry (ICP-SFMS) and alpha-spectrometry is described. The developed procedure involves a selective CaF 2 co-precipitation for preconcentration followed by extraction chromatographic separation. The proposed method effectively eliminates the possible interferences in mass spectrometric analysis and also removes interfering radionuclides that may disturb alpha-spectrometric measurement. For 239 Pu, 240 Pu and 241 Pu limits of detection of 9.0 fg x g -1 (0.021 mBq), 1.7 fg x g -1 (0.014 mBq) and 3.1 fg x g -1 (11.9 mBq) were achieved by ICP-SFMS, respectively, and 0.02 mBq by alpha-spectrometry. Results of certified reference materials agreed well with the recommended values. (author)

Levels of tritium concentration in the environmental samples around JAERI TOKAI

International Nuclear Information System (INIS)

Matsuura, K.; Sasa, Y.; Nakamura, C.; Katagiri, H.

1995-01-01

By the operation of research reactors, tritium-handling facilities, nuclear power plants, and a reprocessing facility around JAERI TOKAI, tritium is released into the environment in compliance with the regulatory standards. To investigate the levels of tritium concentration in environmental samples around JAERI, rain, air (vapor and hydrogen gas), and tissue-free water of pine needles were measured and analyzed from 1984 to 1993. Sampling locations were determined by taking into consideration wind direction, distance from nuclear facilities, and population distribution. The NAKA site (about 6 km west-northwest from the Tokai site) was also selected as a reference point. Rain and tissue-free water of pine needles were sampled monthly. For air samples, sampling was carried out for two weeks by using the continuous tritium sampler. After the pretreatment of samples, tritium concentrations were measured by a low background liquid scintillation counter (detection limit 0.8 Bq/l). Annual mean tritium concentrations in rain observed at six points for 10 years was 0.8 to 8.9 Bq/l, which decreased with distance from the nuclear facilities. Tritium concentrations in rain obtained at Chiba City were around 0.8 Bq/l (1987-1988) and those at the NAKA site were 0.8 to 3.8 Bq/l. Annual mean HTO concentrations in air at three points for 10 years were 9.2 x 10 -2 to 1.1 Bq/m 3 , although HT concentrations in air, ranging from 1.7 x 10 -2 to 5.8 x 10 -2 Bq/m 3 , were not influenced by the operation of the nuclear facilities. Annual mean tritium concentrations in tissue-free water of pine needles at four points for 10 years were 1.4 to 31 Bq/l. Those at the NAKA site ranging from 1.4 to 6.2 Bq/l were in good agreement with the reported value by Takashima of 0.78 to 3.0 Bq/l at twenty-one locations in Japan. Monthly mean HTO concentrations in air for 10 years showed a good correlation with absolute humidity, while other samples showed no seasonal variation. Higher level tritium

Improved analytical sensitivity for uranium and plutonium in environmental samples: Cavity ion source thermal ionization mass spectrometry

International Nuclear Information System (INIS)

Ingeneri, Kristofer; Riciputi, L.

2001-01-01

Following successful field trials, environmental sampling has played a central role as a routine part of safeguards inspections since early 1996 to verify declared and to detect undeclared activity. The environmental sampling program has brought a new series of analytical challenges, and driven a need for advances in verification technology. Environmental swipe samples are often extremely low in concentration of analyte (ng level or lower), yet the need to analyze these samples accurately and precisely is vital, particularly for the detection of undeclared nuclear activities. Thermal ionization mass spectrometry (TIMS) is the standard method of determining isotope ratios of uranium and plutonium in the environmental sampling program. TIMS analysis typically employs 1-3 filaments to vaporize and ionize the sample, and the ions are mass separated and analyzed using magnetic sector instruments due to their high mass resolution and high ion transmission. However, the ionization efficiency (the ratio of material present to material actually detected) of uranium using a standard TIMS instrument is low (0.2%), even under the best conditions. Increasing ionization efficiency by even a small amount would have a dramatic impact for safeguards applications, allowing both improvements in analytical precision and a significant decrease in the amount of uranium and plutonium required for analysis, increasing the sensitivity of environmental sampling