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Sample records for water samples floatation

  1. Ionic liquid foam floatation coupled with ionic liquid dispersive liquid-liquid microextraction for the separation and determination of estrogens in water samples by high-performance liquid chromatography with fluorescence detection.

    Science.gov (United States)

    Zhang, Rui; Wang, Chuanliu; Yue, Qiaohong; Zhou, Tiecheng; Li, Na; Zhang, Hanqi; Hao, Xiaoke

    2014-11-01

    An ionic liquid foam floatation coupled with ionic liquid dispersive liquid-liquid microextraction method was proposed for the extraction and concentration of 17-α-estradiol, 17-β-estradiol-benzoate, and quinestrol in environmental water samples by high-performance liquid chromatography with fluorescence detection. 1-Hexyl-3-methylimidazolium tetrafluoroborate was applied as foaming agent in the foam flotation process and dispersive solvent in microextraction. The introduction of the ion-pairing and salting-out agent NH4 PF6 was beneficial to the improvement of recoveries for the hydrophobic ionic liquid phase and analytes. Parameters of the proposed method including concentration of 1-hexyl-3-methylimidazolium tetrafluoroborate, flow rate of carrier gas, floatation time, types and concentration of ionic liquids, salt concentration in samples, extraction time, and centrifugation time were evaluated. The recoveries were between 98 and 105% with relative standard deviations lower than 7% for lake water and well water samples. The isolation of the target compounds from the water was found to be efficient, and the enrichment factors ranged from 4445 to 4632. This developing method is free of volatile organic solvents compared with regular extraction. Based on the unique properties of ionic liquids, the application of foam floatation, and dispersive liquid-liquid microextraction was widened. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  2. Examining the short-term anxiolytic and antidepressant effect of Floatation-REST.

    Science.gov (United States)

    Feinstein, Justin S; Khalsa, Sahib S; Yeh, Hung-Wen; Wohlrab, Colleen; Simmons, W Kyle; Stein, Murray B; Paulus, Martin P

    2018-01-01

    Floatation-REST (Reduced Environmental Stimulation Therapy) reduces sensory input to the nervous system through the act of floating supine in a pool of water saturated with Epsom salt. The float experience is calibrated so that sensory signals from visual, auditory, olfactory, gustatory, thermal, tactile, vestibular, gravitational and proprioceptive channels are minimized, as is most movement and speech. This open-label study aimed to examine whether Floatation-REST would attenuate symptoms of anxiety, stress, and depression in a clinical sample. Fifty participants were recruited across a spectrum of anxiety and stress-related disorders (posttraumatic stress, generalized anxiety, panic, agoraphobia, and social anxiety), most (n = 46) with comorbid unipolar depression. Measures of self-reported affect were collected immediately before and after a 1-hour float session, with the primary outcome measure being the pre- to post-float change score on the Spielberger State Anxiety Inventory. Irrespective of diagnosis, Floatation-REST substantially reduced state anxiety (estimated Cohen's d > 2). Moreover, participants reported significant reductions in stress, muscle tension, pain, depression and negative affect, accompanied by a significant improvement in mood characterized by increases in serenity, relaxation, happiness and overall well-being (p Floatation-REST may be a promising technique for transiently reducing the suffering in those with anxiety and depression. ClinicalTrials.gov NCT03051074.

  3. Examining the short-term anxiolytic and antidepressant effect of Floatation-REST

    Science.gov (United States)

    Khalsa, Sahib S.; Yeh, Hung-wen; Wohlrab, Colleen; Simmons, W. Kyle; Stein, Murray B.; Paulus, Martin P.

    2018-01-01

    Floatation-REST (Reduced Environmental Stimulation Therapy) reduces sensory input to the nervous system through the act of floating supine in a pool of water saturated with Epsom salt. The float experience is calibrated so that sensory signals from visual, auditory, olfactory, gustatory, thermal, tactile, vestibular, gravitational and proprioceptive channels are minimized, as is most movement and speech. This open-label study aimed to examine whether Floatation-REST would attenuate symptoms of anxiety, stress, and depression in a clinical sample. Fifty participants were recruited across a spectrum of anxiety and stress-related disorders (posttraumatic stress, generalized anxiety, panic, agoraphobia, and social anxiety), most (n = 46) with comorbid unipolar depression. Measures of self-reported affect were collected immediately before and after a 1-hour float session, with the primary outcome measure being the pre- to post-float change score on the Spielberger State Anxiety Inventory. Irrespective of diagnosis, Floatation-REST substantially reduced state anxiety (estimated Cohen’s d > 2). Moreover, participants reported significant reductions in stress, muscle tension, pain, depression and negative affect, accompanied by a significant improvement in mood characterized by increases in serenity, relaxation, happiness and overall well-being (p < .0001 for all variables). In reference to a group of 30 non-anxious participants, the effects were found to be more robust in the anxious sample and approaching non-anxious levels during the post-float period. Further analysis revealed that the most severely anxious participants reported the largest effects. Overall, the procedure was well-tolerated, with no major safety concerns stemming from this single session. The findings from this initial study need to be replicated in larger controlled trials, but suggest that Floatation-REST may be a promising technique for transiently reducing the suffering in those with anxiety and

  4. Examining the short-term anxiolytic and antidepressant effect of Floatation-REST.

    Directory of Open Access Journals (Sweden)

    Justin S Feinstein

    Full Text Available Floatation-REST (Reduced Environmental Stimulation Therapy reduces sensory input to the nervous system through the act of floating supine in a pool of water saturated with Epsom salt. The float experience is calibrated so that sensory signals from visual, auditory, olfactory, gustatory, thermal, tactile, vestibular, gravitational and proprioceptive channels are minimized, as is most movement and speech. This open-label study aimed to examine whether Floatation-REST would attenuate symptoms of anxiety, stress, and depression in a clinical sample. Fifty participants were recruited across a spectrum of anxiety and stress-related disorders (posttraumatic stress, generalized anxiety, panic, agoraphobia, and social anxiety, most (n = 46 with comorbid unipolar depression. Measures of self-reported affect were collected immediately before and after a 1-hour float session, with the primary outcome measure being the pre- to post-float change score on the Spielberger State Anxiety Inventory. Irrespective of diagnosis, Floatation-REST substantially reduced state anxiety (estimated Cohen's d > 2. Moreover, participants reported significant reductions in stress, muscle tension, pain, depression and negative affect, accompanied by a significant improvement in mood characterized by increases in serenity, relaxation, happiness and overall well-being (p < .0001 for all variables. In reference to a group of 30 non-anxious participants, the effects were found to be more robust in the anxious sample and approaching non-anxious levels during the post-float period. Further analysis revealed that the most severely anxious participants reported the largest effects. Overall, the procedure was well-tolerated, with no major safety concerns stemming from this single session. The findings from this initial study need to be replicated in larger controlled trials, but suggest that Floatation-REST may be a promising technique for transiently reducing the suffering in those with

  5. The treatments of soil Rirang by floatation and Acid leaching

    International Nuclear Information System (INIS)

    Kosim-Affandi; Umar-Sarip; Alwi, Guswita; Sri-Sudaryanto

    2000-01-01

    The treatments of soil Rirang by floatation and acid leaching has been carried out to increase high uranium concentrates of materials, separating associated economical minerals and to reduce the gangue minerals which bothering at chemical processing. The physical treatment has been done by ore preparation and floatation using oleic acid and p ine oil , 20 % of pulp at pH 9, condition time at 5 minutes and collections of float fraction was 10 minutes. The chemical processing has been done by dynamic leaching using H 2 SO 4 100 kg/ton, MnO 2 20 kg/ton, 50 % of solid with ore size - 65 mesh, temperature at 80 o C and time of leaching was 8 hours. The result of experiments is as follows : Physical treatment by floatation shown that the concentrates of U increased at sink fraction by (1.5 - 2) times against feed sample for all the samples, and in the float fraction the recovery of molybdenite separation is 58 - 81 % and rare earths is 57 - 80 %. The result of dynamic leaching is 76 - 91 %, and recovery uranium increasing from 81.02 % (mixture samples soil before floatation) to 91.16 % ( mixture samples of float fraction)

  6. The Elicitation of Relaxation and Interoceptive Awareness Using Floatation Therapy in Individuals With High Anxiety Sensitivity.

    Science.gov (United States)

    Feinstein, Justin S; Khalsa, Sahib S; Yeh, Hung-Wen; Al Zoubi, Obada; Arevian, Armen C; Wohlrab, Colleen; Pantino, Marie K; Cartmell, Laci J; Simmons, W Kyle; Stein, Murray B; Paulus, Martin P

    2018-03-09

    Floatation-REST (Reduced Environmental Stimulation Therapy), an intervention that attenuates exteroceptive sensory input to the nervous system, has recently been found to reduce state anxiety across a diverse clinical sample with high levels of anxiety sensitivity (AS). To further examine this anxiolytic effect, the present study investigated the affective and physiological changes induced by Floatation-REST and assessed whether individuals with high AS experienced any alterations in their awareness for interoceptive sensation while immersed in an environment lacking exteroceptive sensation. Using a within-subject crossover design, 31 participants with high AS were randomly assigned to undergo a 90-minute session of Floatation-REST or an exteroceptive comparison condition. Measures of self-reported affect and interoceptive awareness were collected before and after each session, and blood pressure was measured during each session. Relative to the comparison condition, Floatation-REST generated a significant anxiolytic effect characterized by reductions in state anxiety and muscle tension and increases in feelings of relaxation and serenity (p 12 mm Hg). The float environment also significantly enhanced awareness and attention for cardiorespiratory sensations. Floatation-REST induced a state of relaxation and heightened interoceptive awareness in a clinical sample with high AS. The paradoxical nature of the anxiolytic effect in this sample is discussed in relation to Wolpe's theory of reciprocal inhibition and the regulation of distress via sustained attention to present moment visceral sensations such as the breath. Copyright © 2018 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.

  7. Density measurements of small amounts of high-density solids by a floatation method

    International Nuclear Information System (INIS)

    Akabori, Mitsuo; Shiba, Koreyuki

    1984-09-01

    A floatation method for determining the density of small amounts of high-density solids is described. The use of a float combined with an appropriate floatation liquid allows us to measure the density of high-density substances in small amounts. Using the sample of 0.1 g in weight, the floatation liquid of 3.0 g cm -3 in density and the float of 1.5 g cm -3 in apparent density, the sample densities of 5, 10 and 20 g cm -3 are determined to an accuracy better than +-0.002, +-0.01 and +-0.05 g cm -3 , respectively that correspond to about +-1 x 10 -5 cm 3 in volume. By means of appropriate degassing treatments, the densities of (Th,U)O 2 pellets of --0.1 g in weight and --9.55 g cm -3 in density were determined with an accuracy better than +-0.05 %. (author)

  8. Clarifying the Misconception about the Principle of Floatation

    Science.gov (United States)

    Yadav, Manoj K.

    2014-01-01

    This paper aims to clarify the misconception about the violation of the principle of floatation. Improper understanding of the definition of "displaced fluid" by a floating body leads to the misconception. With the help of simple experiments, this article shows that there is no violation of the principle of floatation.

  9. Developing Water Sampling Standards

    Science.gov (United States)

    Environmental Science and Technology, 1974

    1974-01-01

    Participants in the D-19 symposium on aquatic sampling and measurement for water pollution assessment were informed that determining the extent of waste water stream pollution is not a cut and dry procedure. Topics discussed include field sampling, representative sampling from storm sewers, suggested sampler features and application of improved…

  10. Sinking/floatation of pipelines and other objects in liquefied soil under waves

    DEFF Research Database (Denmark)

    Sumer, B. Mutlu; Fredsøe, Jørgen; Christensen, S.

    1999-01-01

    , and the experiments with the structure model (a pipeline, a sphere, and a cube). In the former experiments, the pore-water pressure was measured across the soil depth. The pore-water pressure built up, as the waves progressed. The soil was liquefied for wave heights larger than a critical value. Regarding......This paper presents the results of an experimental study where the sinking and floatation of a pipeline and other objects (namely, a sphere and a cube) in a silt bed was investigated. The bed was exposed to progressive waves. Two kinds of experiments were made: The undisturbed-flow experiments...... the experiments with the structure model, the displacement of the structure (sinking or floatation) was measured simultaneously with the pore-water pressure. The influence of various parameters (such as the initial position of the object, the specific gravity, the soil layer thickness, and the wave height...

  11. The effects of leaching and floatation on the ash fusion temperatures of three selected lignites

    Energy Technology Data Exchange (ETDEWEB)

    Feng-hai Li; Jie-jie Huang; Yi-tian Fang; Yang Wang [Chinese Academy of Sciences, Taiyuan (China). Institute of Coal Chemistry

    2011-07-15

    Experiments have been conducted with Huolinhe (HLH), Xiaolongtan (XLT), and Ethiopian (ET) lignites to investigate the effects of washing with water, acid-leaching, and floatation on their ash fusion temperatures (AFTs). The results show that the AFTs of XLT and ET are elevated by washing with water and floatation, but the AFT of HLH is decreased. The AFTs of all three lignites are increased markedly by acid leaching. A decrease in the total basic composition in ash increases its AFT, and vice versa. Changes in the mineral contents of the coals after treatment contribute to the variations in their AFTs. After washing with water, the lower AFT of HLH is brought about by the increases in the amounts of cordierite and anhydrite, whereas the higher AFT of XLT is caused by the decreases in the amounts of anhydrite and calcite. For the floatation treatment, the decrease of AFT for HLH is due to the reduction in the amount of kaolinite, but the elevation of AFT for XLT or ET is caused by the decrease in the amount of pyrite and the reductions in the amounts of gypsum and xanthoxenite, respectively. For the acid-leaching treatment, a decrease in the amount of pyrite and an increase in the amount of kaolinite result in increases in AFTs for HLH and XLT. Increases in the amounts of kaolinite and cristobalite in FET (ET after floatation), WET (ET after washing with water), and AET (ET after acid-leaching) lead to corresponding increases in the AFTs. 27 refs., 10 figs., 3 tabs.

  12. Reactor water sampling device

    International Nuclear Information System (INIS)

    Sakamaki, Kazuo.

    1992-01-01

    The present invention concerns a reactor water sampling device for sampling reactor water in an in-core monitor (neutron measuring tube) housing in a BWR type reactor. The upper end portion of a drain pipe of the reactor water sampling device is attached detachably to an in-core monitor flange. A push-up rod is inserted in the drain pipe vertically movably. A sampling vessel and a vacuum pump are connected to the lower end of the drain pipe. A vacuum pump is operated to depressurize the inside of the device and move the push-up rod upwardly. Reactor water in the in-core monitor housing flows between the drain pipe and the push-up rod and flows into the sampling vessel. With such a constitution, reactor water in the in-core monitor housing can be sampled rapidly with neither opening the lid of the reactor pressure vessel nor being in contact with air. Accordingly, operator's exposure dose can be reduced. (I.N.)

  13. Separation of monazite from Rirang ore by floatation method

    International Nuclear Information System (INIS)

    Affandi, Kosim; Sjahminan, Mainar

    1995-01-01

    Separation of monazite from Rirang ore has been carried out by means of floatation using oleic acid and pine oil as promoter and frothier reagents, respectively. Several parameters affecting floatation process, i.e. grain size of the ore, pulp pH, and reagents concentration were examnined. The optimal conditions for the process include the use of -100 mesh feed ore, pulp pH 9.0 and 1 kilogram of each oleic acid and pine oil per tonne ore. Based on the conditions, monazite recovery of 90% was achieved with about 20% uranium remain in monazite concentrate. (author). 7 refs, 9tabs, 1 fig

  14. Application of solvent floatation to separation and determination of triazine herbicides in honey by high-performance liquid chromatography.

    Science.gov (United States)

    Wang, Kun; Jiang, Jia; Lv, Xinping; Zang, Shuang; Tian, Sizhu; Zhang, Hanqi; Yu, Aimin; Zhang, Ziwei; Yu, Yong

    2018-03-01

    Based on the foaming property of the honey, a rapid, simple, and effective method solvent floatation (SF) was developed and firstly applied to the extraction and separation of triazine herbicides in honey. The analytes were determined by high-performance liquid chromatography. Some parameters affecting the extraction efficiencies, such as the type and volume of extraction solvent, type of salt, amount of (NH 4 ) 2 SO 4 , pH value of sample solution, gas flow rate, and floatation time, were investigated and optimized. The limits of detection for analytes are in the range of 0.16-0.56 μg kg -1 . The recoveries and relative standard deviations for determining triazines in five real honey samples are in the range of 78.2-112.9 and 0.2-9.2%, respectively.

  15. A pilot study to evaluate the effects of floatation spa treatment on patients with osteoarthritis.

    Science.gov (United States)

    Hill, S; Eckett, M J; Paterson, C; Harkness, E F

    1999-12-01

    To conduct a preliminary investigation of the effects on floatation spa therapy on quality of life in patients with osteoarthritis to see if controlled trials are warranted. Uncontrolled clinical trial. Private floatation spa therapy centre. Fourteen patients with chronic osteoarthritis of the weight-bearing joints, of whom four dropped out. Six weekly sessions of floatation spa therapy. SF36, AIMS2 and MYMOP quality-of-life questionnaires. All patients improved. Differences between baseline and discharge scores showed statistically significant improvement for MYMOP, but not AIMS2 or SF-36. Controlled trials of floatation spa therapy for patients with osteoarthritis are warranted.

  16. Effect of reagent type on the froth floatation of Sokoto phosphate ore

    Directory of Open Access Journals (Sweden)

    U.A. Hassan

    2016-06-01

    Full Text Available Effect of reagent type on the froth floatation of Sokoto phosphate ore for its beneficiation has been established. The samples of the Sokoto phosphate mineral ore used for the research work were sourced from mining locations in Dange-Shuni, Bodinga, Yabo, Wurno, and Rabbah Local Government Areas of Sokoto State. Size-Assay analysis conducted on scrubbed Sokoto Phosphates nodules revealed that nodules had a size distribution with 80% passing 29.3 mm. Flotation Tests using AERO704 (fatty Acid, Alkyl Hydroxamates, Melamine as collectors (alone or mixed with diesel, MIBC as frother, Calcium Hydroxide and Sulphuric Acid as pH regulators and Dextrin, Sodium Silicate and Aluminium Chloride as depressants produced poor P2O5 separation in the flotation products due to very poor liberation associated with very fine mineral grains. Based on the results obtained, AERO704 Collector gave the best result with aP2O5 recovery pH of 10.

  17. Identifying The Target Market For a New Floatation Therapy Service, Flowtion

    OpenAIRE

    Varpomaa, Jerry

    2016-01-01

    The purpose of this thesis was to probe and identify the most potential target market for a new kind of wellness-service for Flowtion, a state-of-the-art floatation therapy center, focusing on floatation tanks. To accomplish the main goal for this thesis, a survey was conducted using “Google Forms”. The survey was spread through social media (Facebook), and as a result 41 people answered. The survey helps Flowtion to define their most potential target segment, their behaviour and profile vari...

  18. Radon measurement in Malaysia water samples

    International Nuclear Information System (INIS)

    Ibrahim, A.B.; Rosli Mahat; Yusof Md Amin

    1995-01-01

    This paper reported the results of the measurement of radon in local water. The water samples collected were rainwater, river water, seawater, well water or ground water at area of State of Selangor and Kuala Lumpur. The samples were collected in scintillation cell ZnS(Ag) through Radon Degassing Unit RDU 200. Alpha activity was counted with scintillation counters RD 200 at energy 5.5 MeV. (author)

  19. Water born pollutants sampling using porous suction samples

    International Nuclear Information System (INIS)

    Baig, M.A.

    1997-01-01

    The common standard method of sampling water born pollutants in the vadoze zone is core sampling and it is followed by extraction of pore fluid. This method does not allow sampling at the same location next time and again later on. There is an alternative approach for sampling fluids (water born pollutants) from both saturated and unsaturated regions of vadose zone using porous suction samplers. There are three types of porous suction samplers, vacuum-operated, pressure-vacuum lysimeters, high pressure vacuum samples. The suction samples are operated in the range of 0-70 centi bars and usually consist of ceramic and polytetrafluorethylene (PTFE). The operation range of PTFE is higher than ceramic cups. These samplers are well suited for in situ and repeated sampling form the same location. This paper discusses the physical properties and operating condition of such samplers to the utilized under our environmental sampling. (author)

  20. Determination of Phthalates in Drinking Water Samples

    African Journals Online (AJOL)

    user

    successfully applied to the analysis of phthalate esters contamination in bottled drinking water samples. ... esters are used in the manufacturing of polyvinyl chloride. (PVC). ... water, soil, air, food products and the human body. (Castillo et al.

  1. Water sample-collection and distribution system

    Science.gov (United States)

    Brooks, R. R.

    1978-01-01

    Collection and distribution system samples water from six designated stations, filtered if desired, and delivers it to various analytical sensors. System may be controlled by Water Monitoring Data Acquisition System or operated manually.

  2. 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)

  3. Selective floatation-spectrophotometric determination of tellurium (4) with papaverine and butyl rhodamine B

    International Nuclear Information System (INIS)

    Skripchuk, V.G.

    1981-01-01

    It is shown, that papaverine reacts with a bromide complex of tellurium (4) to form a compound readily floated by toluene. The floatation is carried out from an aqueous solution, 5.2 M in H 2 SO 4 , 0.2 M in KBr and 5.4x10 -3 M in papaverine. The absorbance is a function of tellurium (4) concentration over a range of 5-100 μg Te/5 ml. Such a highly sensitive reagent as butylrhodamine B can be effectively substituted for papaverine. The floatation results in better selectivity. The method makes it possible to determine tellurium in blister, anodic and cathodic copper without matrix preseparation [ru

  4. Water Sample Points, Navajo Nation, 2000, USACE

    Data.gov (United States)

    U.S. Environmental Protection Agency — This point shapefile presents the locations and results for water samples collected on the Navajo Nation by the US Army Corps of Engineers (USACE) for the US...

  5. Water sampling techniques for continuous monitoring of pesticides in water

    Directory of Open Access Journals (Sweden)

    Šunjka Dragana

    2017-01-01

    Full Text Available Good ecological and chemical status of water represents the most important aim of the Water Framework Directive 2000/60/EC, which implies respect of water quality standards at the level of entire river basin (2008/105/EC and 2013/39/EC. This especially refers to the control of pesticide residues in surface waters. In order to achieve the set goals, a continuous monitoring program that should provide a comprehensive and interrelated overview of water status should be implemented. However, it demands the use of appropriate analysis techniques. Until now, the procedure for sampling and quantification of residual pesticide quantities in aquatic environment was based on the use of traditional sampling techniques that imply periodical collecting of individual samples. However, this type of sampling provides only a snapshot of the situation in regard to the presence of pollutants in water. As an alternative, the technique of passive sampling of pollutants in water, including pesticides has been introduced. Different samplers are available for pesticide sampling in surface water, depending on compounds. The technique itself is based on keeping a device in water over a longer period of time which varies from several days to several weeks, depending on the kind of compound. In this manner, the average concentrations of pollutants dissolved in water during a time period (time-weighted average concentrations, TWA are obtained, which enables monitoring of trends in areal and seasonal variations. The use of these techniques also leads to an increase in sensitivity of analytical methods, considering that pre-concentration of analytes takes place within the sorption medium. However, the use of these techniques for determination of pesticide concentrations in real water environments requires calibration studies for the estimation of sampling rates (Rs. Rs is a volume of water per time, calculated as the product of overall mass transfer coefficient and area of

  6. The WIPP Water Quality Sampling Program

    International Nuclear Information System (INIS)

    Uhland, D.; Morse, J.G.; Colton, D.

    1986-01-01

    The Waste Isolation Pilot Plant (WIPP), a Department of Energy facility, will be used for the underground disposal of wastes. The Water Quality Sampling Program (WQSP) is designed to obtain representative and reproducible water samples to depict accurate water composition data for characterization and monitoring programs in the vicinity of the WIPP. The WQSP is designed to input data into four major programs for the WIPP project: Geochemical Site Characterization, Radiological Baseline, Environmental Baseline, and Performance Assessment. The water-bearing units of interest are the Culebra and Magneta Dolomite Members of the Rustler Formation, units in the Dewey Lake Redbeds, and the Bell Canyon Formation. At least two chemically distinct types of water occur in the Culebra, one being a sodium/potassium chloride water and the other being a calcium/magnesium sulfate water. Water from the Culebra wells to the south of the WIPP site is distinctly fresher and tends to be of the calcium/magnesium sulfate type. Water in the Culebra in the north and around the WIPP site is distinctly fresher and tends to be of the sodium/potassium chloride type and is much higher in total dissolved solids. The program, which is currently 1 year old, will continue throughout the life of the facility as part of the Environmental Monitoring Program

  7. Portable field water sample filtration unit

    International Nuclear Information System (INIS)

    Hebert, A.J.; Young, G.G.

    1977-01-01

    A lightweight back-packable field-tested filtration unit is described. The unit is easily cleaned without cross contamination at the part-per-billion level and allows rapid filtration of boiling hot and sometimes muddy water. The filtration results in samples that are free of bacteria and particulates and which resist algae growth even after storage for months. 3 figures

  8. Water sampling device for detecting fuel failure

    International Nuclear Information System (INIS)

    Masubuchi, Yukio.

    1997-01-01

    A notched portion is formed at the lower end of an outer cap, and an extensible air bag is disposed being in contact with the inner side of the notched portion. A compressed air is sent into the outer gap through an air supply pipe to urge coolants thereby lowering the water level. A portion of the compressed air gets out of the outer gap from the notched portion, and if air bubbles are observed on the surface of coolants in a pressure vessel of a reactor, the outer cap is confirmed to be attached to the upper lattice plate. Compressed air is supplied to the air bag to close the notched portion. Then, coolants are sucked from a water level confirmation pipe. The level of coolants is further lowered, and the compressed air is sucked from the water level confirmation pipe instead of the coolants. Then, the level of the coolants at the inner side of the inner cap is confirmed to be made lower than the upper end of the channel box of a reactor fuel assembly. Then, coolants in the channel box are sampled, as a specimen water, through a water sampling pipe. (I.N.)

  9. PIXE analysis applied to characterized water samples

    International Nuclear Information System (INIS)

    Santos, Maristela S.; Carneiro, Luana Gomes; Medeiros, Geiza; Sampaio, Camilla; Martorell, Ana Beatriz Targino; Gouvea, Stella; Cunha, Kenya Moore Dias da

    2011-01-01

    Araxa, in Brazil, is a naturally high background area located in the State of Minas Gerais with a population of about 93 672 people. Araxa is historical city famous for its mineral water sources and mud from Termas de Araxa spa, which have been used for therapeutic, and recreation purposes. Other important aspect of economy of the city are mining and metallurgic industries. In the Araxa area is located the largest deposit of pyrochlore, a niobium mineral, and also a deposit of apatite, a phosphate mineral both containing Th and U associated to crystal lattice. The minerals are obtained from open pit mines, the minerals are processed in industrial also located in city of Araxa, these plants process the pyrochlore and apatite to obtain the Fe-Nb alloy and the concentrate of phosphate, respectively. Studies were developed in this area to assessment the occupational risk of the workers due to exposure to dust particles during the routine working, however very few studies evaluated the water contamination outside the mines in order to determine the metal (stables elements) concentrations in water and also the concentrations of the radionuclides in water. This paper presents the previous results of a study to identify and determine the concentrations of metals (stables elements) and radionuclides in river around the city. The water from these rivers is used as drinking water and irrigation water. The water samples were collected in different rivers around the Araxa city and the samples were analyzed using PIXE technique. A proton beam of 2 MeV obtained from the van de Graaff electrostatic accelerator was used to induce the characteristic X-rays. S, K, Ca, Cr, Mn, Fe, Ni, Zn, Ba, Pb and U were identified in the mass spectrum of the samples. The elemental mass concentrations were compared using a non-parametric statistical test. The results of the statistical test showed that the elemental mass concentrations did not present the same distribution. These results indicated

  10. Determination of 40K in water samples

    International Nuclear Information System (INIS)

    Delgado, C. E.; Miranda C, L.; Cuevas J, A. K.; Vega C, H. R.

    2014-10-01

    The natural water used for human consumption comes from different sources, which may contain suspended solids in varying proportions. In groundwater, the source of suspended solids is related to the dissolution of mineral strata by the waters and leaching of rocks. Also, the radioactivity could concentrate on the bodies of slow-moving water that eventually could present a risk to ecosystems, as well as for the consumer. The water usually contains several natural radionuclides as: tritium, radon, radio, uranium isotopes, etc. The objective of this study was to evaluate the concentration of 40 K in water from different areas of Zacatecas state (Mexico). Four water samples were taken in triplicate from different areas; the 40 K concentration was measured with a spectrum metric system of gamma radiation with NaI (Tl) scintillation detector of 7.62 cm. In the measuring process a standard was prepared using water and KCl analytic grade where the 40 K concentration is 6.25 mol/Lt adding 250 mg/ml of potassium. Also the system was calibrated in energy using 3 point sources of 137 Cs, diameter 22 Na and 7.62 cm of height, using containers Marinelli and 60 Co. In the obtained spectra was observed that the photon of 1.432 MeV that emits the 40 K when decaying is the most important. The highest concentration was of 123 ± 5.2 Bq/lt and the lowest was of 9 ± 0.4 Bq/lt. Under the standards of drinking water, an amount of 40 K deposits an effective dose which contributes to annual dose received by people. (Author)

  11. Investigative studies on water contamination in Bangladesh. Primary treatment of water samples at the sampling site

    International Nuclear Information System (INIS)

    Sera, K.; Islam, Md. Shafiqul; Takatsuji, T.; Nakamura, T.; Goto, S.; Takahashi, C.; Saitoh, Y.

    2010-01-01

    Arsenic concentration in 13 well waters, 9 pond waters, 10 agricultural waters and a coconut juice taken in Comilla district, Bangladesh, where the problem of arsenic pollution is the most severe, was investigated. High-level arsenic is detected even in the well water which has been kept drinking by the people. Relatively high arsenic concentration was detected for some pond and farm waters even though the sampling was performed just after the rainy season and the waters were expected to be highly diluted. Clear relationship was observed in elemental compositions between the pond water and the coconut juice collected at the edge of the water. These results are expected to become the basic information for evaluating the risk of individual food such as cultured fishes, shrimps and farm products, and for controlling total intakes of arsenic. In order to solve the problem of transportation of water samples internationally, a simple method of target preparation performed at the sampling site was established and its validity was confirmed. All targets were prepared at the sampling sites in this study on the basis of this method. (author)

  12. Water evaporation: a transition path sampling study.

    Science.gov (United States)

    Varilly, Patrick; Chandler, David

    2013-02-07

    We use transition path sampling to study evaporation in the SPC/E model of liquid water. On the basis of thousands of evaporation trajectories, we characterize the members of the transition state ensemble (TSE), which exhibit a liquid-vapor interface with predominantly negative mean curvature at the site of evaporation. We also find that after evaporation is complete, the distributions of translational and angular momenta of the evaporated water are Maxwellian with a temperature equal to that of the liquid. To characterize the evaporation trajectories in their entirety, we find that it suffices to project them onto just two coordinates: the distance of the evaporating molecule to the instantaneous liquid-vapor interface and the velocity of the water along the average interface normal. In this projected space, we find that the TSE is well-captured by a simple model of ballistic escape from a deep potential well, with no additional barrier to evaporation beyond the cohesive strength of the liquid. Equivalently, they are consistent with a near-unity probability for a water molecule impinging upon a liquid droplet to condense. These results agree with previous simulations and with some, but not all, recent experiments.

  13. Study on extraction of uranium from clayey sandstone with floatation-leaching process

    International Nuclear Information System (INIS)

    Meng Guangshou; Zhao Manchang; Wu Peisheng; Song Wenlan; Li Wenxia.

    1985-01-01

    An improved floatation-leaching process is proposed to extract uranium from some clayey sandstone type of ore. By two-step flotation, the ground feed ore can be divided into three urani-ferous sections, i.e., the sulfidic concentrate carrying organic matter, the carbonate concentrate, and the tailings. The sulfidic concentrate is mixed with the tailings and then treated by acid-leaching with the result that 93% uranium extraction can be attained. The excess free acid of the leached slurry is further neutralized with the carbonate concentrate instead of lime commonly used. As a result, approximately 60% uranium extraction can be attained. As a whole, by the flotation-leaching process the acid consumption can be reduced from 200 kg/t down to < 80 kg/t and the uranium extraction can be raised from 85% to 90% as compared with the conventional acid-leaching process

  14. UMTRA project water sampling and analysis plan, Maybell, Colorado

    International Nuclear Information System (INIS)

    1994-06-01

    This water sampling and analysis plan (WSAP) describes planned water sampling activities and provides the regulatory and technical basis for ground water sampling in 1994 at the US Department of Energy's (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project site in Maybell, Colorado. The WSAP identifies and justifies sampling locations, analytical parameters, and sampling frequencies at the site. The ground water data will be used for site characterization and risk assessment. The regulatory basis for the ground water and surface water monitoring activities is derived from the EPA regulations in 40 CFR Part 192 (1993) and the proposed EPA standards of 1987 (52 FR 36000). Sampling procedures are guided by the UMTRA Project standard operating procedures (SOP) (JEG, n.d.), the Technical Approach Document (TAD) (DOE, 1989), and the most effective technical approach for the site. This WSAP also includes a summary and the results of water sampling activities from 1989 through 1992 (no sampling was performed in 1993)

  15. UMTRA water sampling and analysis plan, Green River, Utah

    International Nuclear Information System (INIS)

    Papusch, R.

    1993-12-01

    The purpose of this water sampling and analysis plan (WSAP) is to provide a basis for groundwater and surface water sampling at the Green River Uranium Mill Tailing Remedial Action (UMTRA) Project site. This WSAP identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequency for the monitoring locations

  16. Effect of particle size on the froth floatation of Sokoto phosphate ore

    Directory of Open Access Journals (Sweden)

    U.A. Hassan

    2016-06-01

    Full Text Available Effect of particle size on the froth floatation of Sokoto phosphate ore for its beneficiation has been investigated and established. The research has been conducted using various reagents, pH(s at different sieve size fractions. Bench scale flotation tests were carried out on -250+180μm, -180+106μm, -106+75μm, -75+45μm and -45+38μm particle size fractions after screening in order to determine the optimum flotation feed size distribution using 1 liter Denver flotation cell. The results of the scoping flotation studies using a conditioning Pulp Density of 60%Solids, pH9, 800g/t reagent dosage for AERO704 Promoter (Fatty Acid and flotation pulp density of 28.5% Solids show that +106μm particle size gave the highest assay content of 20.4% P2O5 with a recovery of 76.2% compared to +38μm (19.9%P2O5 and recovery of 43.2% and +180μm (19.4%P2O5 and 24.1% recovery in their floats (concentrates but with no perfect separation as the tailings fraction also contained similar grades with slight differences.

  17. Recovery of Copper from Slow Cooled Ausmelt Furnace Slag by Floatation

    Science.gov (United States)

    Xue, Ping; Li, Guangqiang; Qin, Qingwei

    Ausmelt furnace slag contains about 0.9% Cu (mass %). With increasing the amount of Ausmelt furnace slag, the recovery of copper from it will produce an enormous economic yield. The recovery of copper by floatation from slow cooled Ausmelt furnace slag was studied in this paper. The phases and composition of the slow cooled slag were analyzed. The factors which affected the copper recovery efficiency such as grinding fineness, pH value of flotation medium, different collectors and floating process were investigated. It was shown that the size distribution of the primary grinding and secondary grinding of middling were 75% for particles less than 0.074mm and 82% for particles less than 0.043mm respectively. The closed-circuit experimental results with butyl xanthate as collector in laboratory showed that the copper grade reached 16.11% and the recovery rate of copper reached 69.90% and the copper grade of tailings was only 0.2%.

  18. Par Pond refill water quality sampling

    International Nuclear Information System (INIS)

    Koch, J.W. II; Martin, F.D.; Westbury, H.M.

    1996-08-01

    This study was designed to document anoxia and its cause in the event that the anoxia caused a fish kill. However, no fish kill was observed during this study, and dissolved oxygen and nutrient concentrations generally remained within the range expected for southeastern reservoirs. Par Pond water quality monitoring will continue during the second summer after refill as the aquatic macrophytes become reestablished and nutrients in the sediments are released to the water column

  19. Physico-chemical characteristics of water sample from Aiba Stream ...

    African Journals Online (AJOL)

    This study aimed at assessing the effectiveness of solar distillation in purification of water. The water sample collected from Aiba stream was subjected to double slope solar water distillation unit. The physico- chemical characteristics of the raw sample and the distillate were determined using standard methods. The.

  20. UMTRA project water sampling and analysis plan, Gunnison, Colorado

    International Nuclear Information System (INIS)

    1994-06-01

    This water sampling and analysis plan summarizes the results of previous water sampling activities and the plan for water sampling activities for calendar year 1994. A buffer zone monitoring plan is included as an appendix. The buffer zone monitoring plan is designed to protect the public from residual contamination that entered the ground water as a result of former milling operations. Surface remedial action at the Gunnison Uranium Mill Tailings Remedial Action Project site began in 1992; completion is expected in 1995. Ground water and surface water will be sampled semiannually in 1994 at the Gunnison processing site (GUN-01) and disposal site (GUN-08). Results of previous water sampling at the Gunnison processing site indicate that ground water in the alluvium is contaminated by the former uranium processing activities. Background ground water conditions have been established in the uppermost aquifer (Tertiary gravels) at the Gunnison disposal site. The monitor well locations provide a representative distribution of sampling points to characterize ground water quality and ground water flow conditions in the vicinity of the sites. The list of analytes has been modified with time to reflect constituents that are related to uranium processing activities and the parameters needed for geochemical evaluation. Water sampling will be conducted at least semiannually during and one year following the period of construction activities, to comply with the ground water protection strategy discussed in the remedial action plan (DOE, 1992a)

  1. Analysis of phthalate esters contamination in drinking water samples ...

    African Journals Online (AJOL)

    The optimum condition method was successfully applied to the analysis of phthalate esters contamination in bottled drinking water samples. The concentration of DMP, DEP and DBP in drinking water samples were below allowable levels, while the DEHP concentration in three samples was found to be greater than the ...

  2. Guidelines for sampling fish in inland waters

    National Research Council Canada - National Science Library

    Backiel, Tadeusz; Welcomme, R. L

    1980-01-01

    The book is addressed mainly to Fishery Biologists but it is hoped that Fishing Gear Technologists also can acquire some basic knowledge of sampling problems and procedures which, in turn, can result...

  3. UMTRA project water sampling and analysis plan -- Shiprock, New Mexico

    International Nuclear Information System (INIS)

    1994-02-01

    Water sampling and analysis plan (WSAP) is required for each U.S. Department of Energy (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project site to provide a basis for ground water and surface water sampling at disposal and former processing sites. This WSAP identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequency for the monitoring stations at the Navaho Reservation in Shiprock, New Mexico, UMTRA Project site. The purposes of the water sampling at Shiprock for fiscal year (FY) 1994 are to (1) collect water quality data at new monitoring locations in order to build a defensible statistical data base, (2) monitor plume movement on the terrace and floodplain, and (3) monitor the impact of alluvial ground water discharge into the San Juan River. The third activity is important because the community of Shiprock withdraws water from the San Juan River directly across from the contaminated alluvial floodplain below the abandoned uranium mill tailings processing site

  4. 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)

  5. chemical and microbiological assessment of surface water samples

    African Journals Online (AJOL)

    PROF EKWUEME

    were investigated in this study: Nine samples from different surface water bodies, two samples from two effluent sources ... Ezeagu, Udi, Nkanu, Oji River and some parts of Awgu and Aninri ..... Study of Stream Output from Small Catchments.

  6. Preconcentration NAA for simultaneous multielemental determination in water sample

    International Nuclear Information System (INIS)

    Chatt, A.

    1999-01-01

    Full text: Environment concerns with water, air, land and their interrelationship viz., human beings, fauna and flora. One of the important environmental compartments is water. Elements present in water might face a whole lot of physico-chemical conditions. This poses challenges to measure their total concentrations as well as different species. Preconcentration of the elements present in water samples is a necessary requisites in water analysis. For multi elements concentration measurements, Neutron Activation Analysis (NAA) is one of the preferred analytical techniques due to its sensitivity and selectivity. In this talk preconcentration NAA for multielemental determination in water sample determination will be discussed

  7. Measurement of radioactivity in water samples

    International Nuclear Information System (INIS)

    Richards, L.

    1990-01-01

    Public concern about the levels of radioactivity release to the environment whether authorised discharges or resulting from nuclear accident, has increased in recent years. Consequently there is increasing pressure for reliable data on the distribution of radioactivity and the extent of its intrusion into food chains and water supplies. As a result a number of laboratories not experienced in radioactivity measurements have acquired nucleonic counting equipment. These notes explore the underlying basics and indicate sources of essential data and information which are required for a better understanding of radioactivity measurements. Particular attention is directed to the screening tests which are usually designated ''gross'' alpha and ''gross'' beta activity measurement. (author)

  8. UMTRA project water sampling and analysis plan, Naturita, Colorado

    International Nuclear Information System (INIS)

    1994-04-01

    Surface remedial action is scheduled to begin at the Naturita UMTRA Project processing site in the spring of 1994. No water sampling was performed during 1993 at either the Naturita processing site (NAT-01) or the Dry Flats disposal site (NAT-12). Results of previous water sampling at the Naturita processing site indicate that ground water in the alluvium is contaminated as a result of uranium processing activities. Baseline ground water conditions have been established in the uppermost aquifer at the Dry Flats disposal site. Water sampling activities scheduled for April 1994 include preconstruction sampling of selected monitor wells at the processing site, surface water sampling of the San Miguel River, sampling of several springs/seeps in the vicinity of the disposal site, and sampling of two monitor wells in Coke Oven Valley. The monitor well locations provide sampling points to characterize ground water quality and flow conditions in the vicinity of the sites. The list of analytes has been updated to reflect constituents related to uranium processing activities and the parameters needed for geochemical evaluation. Water sampling will be conducted annually at minimum during the period of construction activities

  9. PCR detection of Burkholderia multivorans in water and soil samples.

    Science.gov (United States)

    Peeters, Charlotte; Daenekindt, Stijn; Vandamme, Peter

    2016-08-12

    Although semi-selective growth media have been developed for the isolation of Burkholderia cepacia complex bacteria from the environment, thus far Burkholderia multivorans has rarely been isolated from such samples. Because environmental B. multivorans isolates mainly originate from water samples, we hypothesized that water rather than soil is its most likely environmental niche. The aim of the present study was to assess the occurrence of B. multivorans in water samples from Flanders (Belgium) using a fast, culture-independent PCR assay. A nested PCR approach was used to achieve high sensitivity, and specificity was confirmed by sequencing the resulting amplicons. B. multivorans was detected in 11 % of the water samples (n = 112) and 92 % of the soil samples (n = 25) tested. The percentage of false positives was higher for water samples compared to soil samples, showing that the presently available B. multivorans recA primers lack specificity when applied to the analysis of water samples. The results of the present study demonstrate that B. multivorans DNA is commonly present in soil samples and to a lesser extent in water samples in Flanders (Belgium).

  10. Microbial Condition of Water Samples from Foreign Fuel Storage Facilities

    International Nuclear Information System (INIS)

    Berry, C.J.

    1998-01-01

    In order to assess the microbial condition of foreign spent nuclear fuel storage facilities and their possible impact on SRS storage basins, twenty-three water samples were analyzed from 12 different countries. Fifteen of the water samples were analyzed and described in an earlier report (WSRC-TR-97-00365 [1]). This report describes nine additional samples received from October 1997 through March 1998. The samples include three from Australia, two from Denmark and Germany and one sample from Italy and Greece. Each water sample was analyzed for microbial content and activity as determined by total bacteria, viable aerobic bacteria, viable anaerobic bacteria, viable sulfate-reducing bacteria, viable acid-producing bacteria and enzyme diversity. The results for each water sample were then compared to all other foreign samples analyzed to date and monthly samples pulled from the receiving basin for off-site fuel (RBOF), at SRS. Of the nine samples analyzed, four samples from Italy, Germany and Greece had considerably higher microbiological activity than that historically found in the RBOF. This microbial activity included high levels of enzyme diversity and the presence of viable organisms that have been associated with microbial influenced corrosion in other environments. The three samples from Australia had microbial activities similar to that in the RBOF while the two samples from Denmark had lower levels of microbial activity. These results suggest that a significant number of the foreign storage facilities have water quality standards that allow microbial proliferation and survival

  11. 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)

  12. Sampling procedure, receipt and conservation of water samples to determine environmental radioactivity

    International Nuclear Information System (INIS)

    Herranz, M.; Navarro, E.; Payeras, J.

    2009-01-01

    The present document informs about essential goals, processes and contents that the subgroups Sampling and Samples Preparation and Conservation believe they should be part of the procedure to obtain a correct sampling, receipt, conservation and preparation of samples of continental, marine and waste water before qualifying its radioactive content.

  13. Radioactivity in waste water samples from COGEMA supplied by Greenpeace

    International Nuclear Information System (INIS)

    Reinen, H.A.J.M.; Kwakman, P.J.M.; Overwater, R.M.W.; Tax, R.B.; Nissan, L.A.

    1999-01-01

    The environmental organization Greenpeace sampled waste water from the reprocessing plant COGEMA in La Hague, France, in May 1999. On request of the Inspection Environmental Hygiene, The Dutch National Institute for Public Health and Environmental Protection (RIVM) determined the radioactivity of the waste water samples. 5 refs

  14. Determination of Phenols in Water Samples using a Supported ...

    African Journals Online (AJOL)

    The sample preparation method was tested for the determination of phenols in river water samples and landfill leachate. Concentrations of phenols in river water were found to be in the range 4.2 μg L–1 for 2-chlorophenol to 50 μg L–1 for 4-chlorophenol. In landfill leachate, 4-chlorophenol was detected at a concentration ...

  15. Measurement of 90Sr in fresh water samples

    International Nuclear Information System (INIS)

    Belanova, A.; Meresova, J.; Svetlik, I.; Tomaskova, L.

    2008-01-01

    This preliminary study show new experimental approach to the determination of the radionuclide 90 Sr in water samples. The new method of dynamic windows utilizing liquid scintillation counting was applied on model and surface water samples. Our results show the demand of separation technique with significantly higher yields. (authors)

  16. Sampling procedure for lake or stream surface water chemistry

    Science.gov (United States)

    Robert Musselman

    2012-01-01

    Surface waters collected in the field for chemical analyses are easily contaminated. This research note presents a step-by-step detailed description of how to avoid sample contamination when field collecting, processing, and transporting surface water samples for laboratory analysis.

  17. UMTRA project water sampling and analysis plan, Grand Junction, Colorado

    International Nuclear Information System (INIS)

    1994-07-01

    Surface remedial action will be completed at the Grand Junction processing site during the summer of 1994. Results of 1993 water sampling indicate that ground water flow conditions and ground water quality at the processing site have remained relatively constant with time. Uranium concentrations in ground water continue to exceed the maximum concentration limits, providing the best indication of the extent of contaminated ground water. Evaluation of surface water quality of the Colorado River indicate no impact from uranium processing activities. No compliance monitoring at the Cheney disposal site has been proposed because ground water in the Dakota Sandstone (uppermost aquifer) is classified as limited-use (Class 111) and because the disposal cell is hydrogeologically isolated from the uppermost aquifer. The following water sampling and water level monitoring activities are planned for calendar year 1994: (i) Semiannual (early summer and late fall) sampling of six existing monitor wells at the former Grand Junction processing site. Analytical results from this sampling will be used to continue characterizing hydrogeochemical trends in background ground water quality and in the contaminated ground water area resulting from source term (tailings) removal. (ii) Water level monitoring of approximately three proposed monitor wells projected to be installed in the alluvium at the processing site in September 1994. Data loggers will be installed in these wells, and water levels will be electronically monitored six times a day. These long-term, continuous ground water level data will be collected to better understand the relationship between surface and ground water at the site. Water level and water quality data eventually will be used in future ground water modeling to establish boundary conditions in the vicinity of the Grand Junction processing site. Modeling results will be used to help demonstrate and document the potential remedial alternative of natural flushing

  18. A Comparison of Soil-Water Sampling Techniques

    Science.gov (United States)

    Tindall, J. A.; Figueroa-Johnson, M.; Friedel, M. J.

    2007-12-01

    The representativeness of soil pore water extracted by suction lysimeters in ground-water monitoring studies is a problem that often confounds interpretation of measured data. Current soil water sampling techniques cannot identify the soil volume from which a pore water sample is extracted, neither macroscopic, microscopic, or preferential flowpath. This research was undertaken to compare values of extracted suction lysimeters samples from intact soil cores with samples obtained by the direct extraction methods to determine what portion of soil pore water is sampled by each method. Intact soil cores (30 centimeter (cm) diameter by 40 cm height) were extracted from two different sites - a sandy soil near Altamonte Springs, Florida and a clayey soil near Centralia in Boone County, Missouri. Isotopically labeled water (O18? - analyzed by mass spectrometry) and bromide concentrations (KBr- - measured using ion chromatography) from water samples taken by suction lysimeters was compared with samples obtained by direct extraction methods of centrifugation and azeotropic distillation. Water samples collected by direct extraction were about 0.25 ? more negative (depleted) than that collected by suction lysimeter values from a sandy soil and about 2-7 ? more negative from a well structured clayey soil. Results indicate that the majority of soil water in well-structured soil is strongly bound to soil grain surfaces and is not easily sampled by suction lysimeters. In cases where a sufficient volume of water has passed through the soil profile and displaced previous pore water, suction lysimeters will collect a representative sample of soil pore water from the sampled depth interval. It is suggested that for stable isotope studies monitoring precipitation and soil water, suction lysimeter should be installed at shallow depths (10 cm). Samples should also be coordinated with precipitation events. The data also indicate that each extraction method be use to sample a different

  19. Monitoring and sampling perched ground water in a basaltic terrain

    International Nuclear Information System (INIS)

    Hubbell, J.M.

    1990-01-01

    Perched ground water zones can provide significant information on water and contaminant movement. This paper presents information about perched ground water obtained from drilling and monitoring at a hazardous and radioactive waste disposal site at the Idaho National Engineering Laboratory. Six of forty-five wells drilled at the Radioactive Waste Management Complex have detected perched water in basalts above sedimentary interbeds. This paper describes the distribution and characteristics of perched ground water. It discusses perched water below the surficial sediments in wells at the RWMC, the characteristics of chemical constituents found in perched water, the implications for contaminant transport in the unsaturated zone of water, and the lateral extent of perched water. Recommendations are made to increase the probability of detecting and sampling low yield perched water zones. 6 refs., 6 figs., 2 tabs

  20. Soil Gas Sample Handling: Evaluation of Water Removal and Sample Ganging

    Energy Technology Data Exchange (ETDEWEB)

    Fritz, Brad G. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Abrecht, David G. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Hayes, James C. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Mendoza, Donaldo P. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2016-10-31

    Soil gas sampling is currently conducted in support of Nuclear Test Ban treaty verification. Soil gas samples are collected and analyzed for isotopes of interest. Some issues that can impact sampling and analysis of these samples are excess moisture and sample processing time. Here we discuss three potential improvements to the current sampling protocol; a desiccant for water removal, use of molecular sieve to remove CO2 from the sample during collection, and a ganging manifold to allow composite analysis of multiple samples.

  1. UMTRA water sampling and analysis plan, Tuba City, Arizona

    International Nuclear Information System (INIS)

    1993-09-01

    The purpose of this document is to provide background, guidance, and justification for fiscal year (FY) 1994 water sampling activities for the uranium mil tailings site at Tuba City, Arizona. This sampling and analysis plan will form the basis for groundwater sampling and analysis work orders to be implemented in FY94

  2. Water sampling device for fuel rod failure monitoring

    International Nuclear Information System (INIS)

    Oogami, Hideaki; Echigoya, Hironori; Matsuoka, Tesshi.

    1991-01-01

    The device of the present invention accurately samples coolants in a channel box as sampling water even if the upper end of the channel box of a fuel assembly is positioned at the same height or lower than the upper end of an upper lattice plate. An existent device comprises an outer cap, an inner cap, an air supply pipe and a water sampling tube. In addition, the device of the present invention comprises a sealing material disposed at the end of the outer cap for keeping liquid sealing with the upper lattice plate and a water level monitoring pipe extended to lower than the inner cap passing through the liquid sealing of the outer cap for sucking the atmosphere in the outer cap. Pressurized air is sent through the air supply pipe, to lower the water level of the coolants in the outer cap and the water level monitoring pipe sucks the pressurized air, by which the inside and the outside of the channel box are partitioned. Subsequently, if the sample water is sampled by a sampling tube, sampling water which enables accurate evaluation for radioactivity concentration in the fuel assembly can be obtained. (I.S.)

  3. Catch me if you can: Comparing ballast water sampling skids to traditional net sampling

    Science.gov (United States)

    Bradie, Johanna; Gianoli, Claudio; Linley, Robert Dallas; Schillak, Lothar; Schneider, Gerd; Stehouwer, Peter; Bailey, Sarah

    2018-03-01

    With the recent ratification of the International Convention for the Control and Management of Ships' Ballast Water and Sediments, 2004, it will soon be necessary to assess ships for compliance with ballast water discharge standards. Sampling skids that allow the efficient collection of ballast water samples in a compact space have been developed for this purpose. We ran 22 trials on board the RV Meteor from June 4-15, 2015 to evaluate the performance of three ballast water sampling devices (traditional plankton net, Triton sampling skid, SGS sampling skid) for three organism size classes: ≥ 50 μm, ≥ 10 μm to Natural sea water was run through the ballast water system and untreated samples were collected using paired sampling devices. Collected samples were analyzed in parallel by multiple analysts using several different analytic methods to quantify organism concentrations. To determine whether there were differences in the number of viable organisms collected across sampling devices, results were standardized and statistically treated to filter out other sources of variability, resulting in an outcome variable representing the mean difference in measurements that can be attributed to sampling devices. These results were tested for significance using pairwise Tukey contrasts. Differences in organism concentrations were found in 50% of comparisons between sampling skids and the plankton net for ≥ 50 μm, and ≥ 10 μm to < 50 μm size classes, with net samples containing either higher or lower densities. There were no differences for < 10 μm organisms. Future work will be required to explicitly examine the potential effects of flow velocity, sampling duration, sampled volume, and organism concentrations on sampling device performance.

  4. UMTRA project water sampling and analysis plan, Tuba City, Arizona

    International Nuclear Information System (INIS)

    1996-02-01

    Planned, routine ground water sampling activities at the U.S. Department of Energy (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project site in Tuba City, Arizona, are described in the following sections of this water sampling and analysis plan (WSAP). This plan identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequency for the stations routinely monitored at the site. The ground water data are used for site characterization and risk assessment. The regulatory basis for routine ground water monitoring at UMTRA Project sites is derived from the U.S. Environmental Protection Agency (EPA) regulations in 40 CFR Part 192 (1994) and the final EPA standards of 1995 (60 FR 2854). Sampling procedures are guided by the UMTRA Project standard operating procedures (SOP) (JEG, n.d.), and the most effective technical approach for the site

  5. Monitoring and sampling perched ground water in a basaltic terrain

    International Nuclear Information System (INIS)

    Hubbell, J.M.

    1990-01-01

    Perched ground water zones are often overlooked in monitoring plans, but they can provide significant information on water and contaminant movement. This paper presents information about perched ground water obtained from drilling and monitoring at a hazardous and radioactive waste disposal site at the Idaho National Engineering Laboratory. Six of forty-five wells drilled at the Radioactive Waste Management Complex have detected perched water in basalts above sedimentary interbeds. Perched water has been detected at depths of 90 and 210 ft below land surface, approximately 370 ft above the regional water table. Eighteen years of water level measurements from one well at a depth of 210 ft indicate a consistent source of water. Water level data indicate a seasonal fluctuation. The maximum water level in this well varies within a 0.5 ft interval, suggesting the water level reaches equilibrium with the inflow to the well at this height. Volatile organic constituents have been detected in concentrations from 1.2 to 1.4 mg/L of carbon tetrachloride. Eight other volatile organics have been detected. The concentrations of organics are consistent with the prevailing theory of movement by diffusion in the gaseous phase. Results of tritium analyses indicate water has moved to a depth of 86 ft in 17 yr. Results of well sampling analyses indicate monitoring and sampling of perched water can be a valuable resource for understanding the hydrogeologic environment of the vadose zone at disposal sites

  6. UMTRA project water sampling and analysis plan, Monument Valley, Arizona

    International Nuclear Information System (INIS)

    1994-04-01

    The Monument Valley Uranium Mill Tailings Remedial Action (UMTRA) Project site in Cane Valley is a former uranium mill that has undergone surface remediation in the form of tailings and contaminated materials removal. Contaminated materials from the Monument Valley (Arizona) UMTRA Project site have been transported to the Mexican Hat (Utah) UMTRA Project site for consolidation with the Mexican Hat tailings. Tailings removal was completed in February 1994. Three geologic units at the site contain water: the unconsolidated eolian and alluvial deposits (alluvial aquifer), the Shinarump Conglomerate (Shinarump Member), and the De Chelly Sandstone. Water quality analyses indicate the contaminant plume has migrated north of the site and is mainly in the alluvial aquifer. An upward hydraulic gradient in the De Chelly Sandstone provides some protection to that aquifer. This water sampling and analysis plan recommends sampling domestic wells, monitor wells, and surface water in April and September 1994. The purpose of sampling is to continue periodic monitoring for the surface program, evaluate changes to water quality for site characterization, and provide data for the baseline risk assessment. Samples taken in April will be representative of high ground water levels and samples taken in September will be representative of low ground water levels. Filtered and nonfiltered samples will be analyzed for plume indicator parameters and baseline risk assessment parameters

  7. Radon in water samples around Ningyo Toge area

    Energy Technology Data Exchange (ETDEWEB)

    Furuta, Sadaaki [Power Reactor and Nuclear Fuel Development Corp., Kamisaibara, Okayama (Japan). Ningyo Toge Works

    1997-02-01

    Radon concentrations of river water and drinking water were surveyed. Water samples were collected from the region around Ningyo-Toge Works which were positioned on a granitic layer having uranium deposit. Each sample was taken using a separating funnel and the radioactivity was counted by liquid scintillation counter (ALOKA, LB-2). Since there were old working places of mine in the region, mine drainages from them were also analyzed. The radon concentration of drinking water from the region ranged from 0.1 to 230 Bq/l. The samples with a higher activity than 100 Bq/l were water from springs or wells and the area of the highest Rn concentration was on a typical granitic layer, suggesting some geographic effects on Rn concentration. Some samples of drinking water had slightly higher levels of Rn, probably due to the utilization of underflow as its source. The mean concentration of Rn became higher in the order; river water, drinking water, mine drainage in the region. In addition, a negative correlation between Rn concentration of water and the river flow rate was observed in this region. (M.N.)

  8. Sampling and Analysis Plan for the 105-N Basin Water

    International Nuclear Information System (INIS)

    R.O. Mahood

    1997-01-01

    This sampling and analysis plan defines the strategy, and field and laboratory methods that will be used to characterize 105-N Basin water. The water will be shipped to the 200 Area Effluent Treatment Facility for treatment and disposal as part of N Reactor deactivation. These analyses are necessary to ensure that the water will meet the acceptance criteria of the ETF, as established in the Memorandum of Understanding for storage and treatment of water from N-Basin (Appendix A), and the characterization requirements for 100-N Area water provided in a letter from ETF personnel (Appendix B)

  9. Validation of single-sample doubly labeled water method

    International Nuclear Information System (INIS)

    Webster, M.D.; Weathers, W.W.

    1989-01-01

    We have experimentally validated a single-sample variant of the doubly labeled water method for measuring metabolic rate and water turnover in a very small passerine bird, the verdin (Auriparus flaviceps). We measured CO 2 production using the Haldane gravimetric technique and compared these values with estimates derived from isotopic data. Doubly labeled water results based on the one-sample calculations differed from Haldane values by less than 0.5% on average (range -8.3 to 11.2%, n = 9). Water flux computed by the single-sample method differed by -1.5% on average from results for the same birds based on the standard, two-sample technique (range -13.7 to 2.0%, n = 9)

  10. Preconcentration of uranium in water samples using dispersive ...

    African Journals Online (AJOL)

    Preconcentration of uranium in water samples using dispersive liquid-liquid micro- extraction coupled with solid-phase extraction and determination with inductively coupled plasma-optical emission spectrometry.

  11. bacteriological analysis of well water samples in sagamu.

    African Journals Online (AJOL)

    Dr Oboro VO

    Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Olabisi Onabanjo University, Ago-Iwoye, Nigeria. *Correspondence. ... All the water samples exceeded the standard limit of the most probable ... or disinfection and this could lead to outbreak of water borne diseases. ... The bottle was brought up to a surface.

  12. Contamination of Ground Water Samples from Well Installations

    DEFF Research Database (Denmark)

    Grøn, Christian; Madsen, Jørgen Øgaard; Simonsen, Y.

    1996-01-01

    Leaching of a plasticizer, N-butylbenzenesulfonamide, from ground water multilevel sampling installations in nylon has been demonstrated. The leaching resulted in concentrations of DOC and apparent AOX, both comparable with those observed in landfill contaminated ground waters. It is concluded...... that nylon should not be used in studies of contamination with organic compounds....

  13. Bacterial contamination of water samples in Gabon, 2013

    Directory of Open Access Journals (Sweden)

    Jonas Ehrhardt

    2017-10-01

    Full Text Available Contamination of water is a major burden in the public health setting of developing countries. We therefore assessed the quality of water samples in Gabon in 2013. The main findings were a contamination rate with coliforms of 13.5% and the detection of a possible environmental reservoir for extended spectrum beta-lactamase-producing bacteria.

  14. Ion Chromatographic Analyses of Sea Waters, Brines and Related Samples

    OpenAIRE

    Nataša Gros

    2013-01-01

    This review focuses on the ion chromatographic methods for the analyses of natural waters with high ionic strength. At the beginning a natural diversity in ionic composition of waters is highlighted and terminology clarified. In continuation a brief overview of other review articles of potential interest is given. A review of ion chromatographic methods is organized in four sections. The first section comprises articles focused on the determination of ionic composition of water samples as com...

  15. Reduction of hexavalent chromium in water samples acidified for preservation

    Science.gov (United States)

    Stollenwerk, K.G.; Grove, D.B.

    1985-01-01

    Reduction of hexavalent chromium, Cr(VI), in water samples, preserved by standard techniques, was investigated. The standard preservation technique for water samples that are to be analyzed for Cr(VI) consists of filtration through a 0.45-??m membrane, acidification to a pH plastic bottles. Batch experiments were conducted to evaluate the effect of H+ concentration, NO2, temperature, and dissolved organic carbon (DOC) on the reduction of Cr(VI) to Cr(III). The rate of reduction of Cr(VI) to Cr(III) increased with increasing NO2, DOC, H+, and temperature. Reduction of Cr(VI) by organic matter occurred in some samples even though the samples were unacidified. Reduction of Cr(VI) is inhibited to an extent by storing the sample at 4??C. Stability of Cr(VI) in water is variable and depends on the other constituents present in the sample. Water samples collected for the determination of Cr(VI) should be filtered (0.45-??m membrane), refrigerated, and analyzed as quickly as possible. Water samples should not be acidified. Measurement of total Cr in addition to Cr(VI) can serve as a check for Cr(VI) reduction. If total Cr is greater than Cr(VI), the possibility that Cr(VI) reduction has occurred needs to be considered.The rate of reduction of Cr(VI) to Cr(III) increased with increasing NO//2, DOC, H** plus , and temperature. Reduction of Cr(VI) by organic matter occurred in some samples even though the samples were unacidified. Reduction of Cr(VI) is inhibited to an extent by storing the sample at 4 degree C. Stability of Cr(VI) in water is variable and depends on the other constituents present in the sample. Water samples collected for the determination of Cr(VI) should be filtered (0. 45- mu m membrane), refrigerated, and analyzed as quickly as possible. Water samples should not be acidified. Measurement of total Cr in addition to Cr(VI) can serve as a check for Cr(VI) reduction. If total Cr is greater than Cr(VI), the possibility that Cr(VI) reduction has occurred needs

  16. UMTRA project water sampling and analysis plan, Mexican Hat, Utah

    International Nuclear Information System (INIS)

    1994-04-01

    The Mexican Hat, Utah, Uranium Mill Tailings Remedial Action (UMTRA) Project site is a former uranium mill that is undergoing surface remediation in the form of on-site tailings stabilization. Contaminated surface materials from the Monument Valley, Arizona, UMTRA Project site have been transported to the Mexican Hat site and are being consolidated with the Mexican Hat tailings. The scheduled completion of the tailings disposal cell is August 1995. Water is found in two geologic units at the site: the Halgaito Shale Formation and the Honaker Trail Formation. The tailings rest on the Halgaito Shale, and water contained in that unit is a result of milling activities and, to a lesser extent, water released from the tailings from compaction during remedial action construction of the disposal cell. Water in the Halgaito Shale flows through fractures and discharges at seeps along nearby arroyos. Flow from the seeps will diminish as water drains from the unit. Ground water in the lower unit, the Honaker Trail Formation, is protected from contamination by an upward hydraulic gradient. There are no nearby water supply wells because of widespread poor background ground water quality and quantity, and the San Juan River shows no impacts from the site. This water sampling and analysis plan (WSAP) recommends sampling six seeps and one upgradient monitor well compared in the Honaker Trail Formation. Samples will be taken in April 1994 (representative of high group water levels) and September 1994 (representative of low ground water levels). Analyses will be performed on filtered samples for plume indicator parameters

  17. Heavy water standards. Qualitative analyses, sample treating, stocking and manipulation

    International Nuclear Information System (INIS)

    Pavelescu, M.; Steflea, D.; Mihancea, I.; Varlam, M.; Irimescu, R.

    1995-01-01

    This paper presents methods and procedures for measuring heavy water concentration, and also sampling, stocking and handling of samples to be analysed. The main concentration analysis methods are: mass spectrometry, for concentrations less then 1%, densitometry, for concentrations within the range 1% - 99% and infrared spectrometry for concentrations above 99%. Procedures of sampling, processing and purification appropriate to these measuring methods were established. 1 Tab

  18. Major inorganic elements in tap water samples in Peninsular Malaysia.

    Science.gov (United States)

    Azrina, A; Khoo, H E; Idris, M A; Amin, I; Razman, M R

    2011-08-01

    Quality drinking water should be free from harmful levels of impurities such as heavy metals and other inorganic elements. Samples of tap water collected from 24 locations in Peninsular Malaysia were determined for inorganic element content. Minerals and heavy metals were analysed by spectroscopy methods, while non-metal elements were analysed using test kits. Minerals and heavy metals determined were sodium, magnesium, potassium, calcium, chromium, manganese, iron, nickel, copper, zinc, arsenic, cadmium and lead while the non-metal elements were fluoride, chloride, nitrate and sulphate. Most of the inorganic elements found in the samples were below the maximum permitted levels recommended by inter-national drinking water standard limits, except for iron and manganese. Iron concentration of tap water from one of the locations was higher than the standard limit. In general, tap water from different parts of Peninsular Malaysia had low concentrations of heavy metals and inorganic elements.

  19. Quality-control design for surface-water sampling in the National Water-Quality Network

    Science.gov (United States)

    Riskin, Melissa L.; Reutter, David C.; Martin, Jeffrey D.; Mueller, David K.

    2018-04-10

    The data-quality objectives for samples collected at surface-water sites in the National Water-Quality Network include estimating the extent to which contamination, matrix effects, and measurement variability affect interpretation of environmental conditions. Quality-control samples provide insight into how well the samples collected at surface-water sites represent the true environmental conditions. Quality-control samples used in this program include field blanks, replicates, and field matrix spikes. This report describes the design for collection of these quality-control samples and the data management needed to properly identify these samples in the U.S. Geological Survey’s national database.

  20. The collection and field chemical analysis of water samples

    International Nuclear Information System (INIS)

    Korte, N.E.; Ealey, D.T.; Hollenbach, M.H.

    1984-01-01

    A successful water sampling program requires a clear understanding of appropriate measurement and sampling procedures in order to obtain reliable field data and representative samples. It is imperative that the personnel involved have a thorough knowledge of the limitations of the techniques being used. Though this seems self-evident, many sampling and field-chemical-analysis programs are still not properly conducted. Recognizing these problems, the Department of Energy contracted with Bendix Field Engineering Corporation through the Technical Measurements Center to develop and select procedures for water sampling and field chemical analysis at waste sites. The fundamental causese of poor field programs are addressed in this paper, largely through discussion of specific field-measurement techniques and their limitations. Recommendations for improvement, including quality-assurance measures, are also presented

  1. A device for fresh water sampling before radioactive measurements

    International Nuclear Information System (INIS)

    Maubert, Henri; Picat, Philippe.

    1982-06-01

    On account of the many field operations carried out by the laboratory, a water sampling device has been developed. This portable autonomous device performs in situ water filtration and concentration on ion exchange resins and activated carbon columns. The device is described and the trapping performance for 8 radionuclides is given. A comparison is made with the so-called evaporation method. The effects of the treatment of the filtrating elements on the radioactive results are studied. This sampling method is very sensitive [fr

  2. Gas-driven pump for ground-water samples

    Science.gov (United States)

    Signor, Donald C.

    1978-01-01

    Observation wells installed for artificial-recharge research and other wells used in different ground-water programs are frequently cased with small-diameter steel pipe. To obtain samples from these small-diameter wells in order to monitor water quality, and to calibrate solute-transport models, a small-diameter pump with unique operating characteristics is required that causes a minimum alternation of samples during field sampling. A small-diameter gas-driven pump was designed and built to obtain water samples from wells of two-inch diameter or larger. The pump is a double-piston type with the following characteristics: (1) The water sample is isolated from the operating gas, (2) no source of electricity is ncessary, (3) operation is continuous, (4) use of compressed gas is efficient, and (5) operation is reliable over extended periods of time. Principles of operation, actual operation techniques, gas-use analyses and operating experience are described. Complete working drawings and a component list are included. Recent modifications and pump construction for high-pressure applications also are described. (Woodard-USGS)

  3. UMTRA project water sampling and analysis plan, Durango, Colorado

    International Nuclear Information System (INIS)

    1994-01-01

    Surface remedial action has been completed at the Uranium Mill Tailings Remedial Action Project in Durango, Colorado. Contaminated soil and debris have been removed from the former processing site and placed in the Bodo Canyon disposal cell. Ground water at the former uranium mill/tailings site and raffinate pond area has been contaminated by the former milling operations. The ground water at the disposal site was not impacted by the former milling operations at the time of the cell's construction. Activities for fiscal 1994 involve ground water sampling and site characterization of the disposal site

  4. Water and steam sampling systems; Provtagningssystem foer vatten och aanga

    Energy Technology Data Exchange (ETDEWEB)

    Hellman, Mats

    2009-10-15

    The supervision of cycle chemistry can be divided into two parts, the sampling system and the chemical analysis. In modern steam generating plants most of the chemical analyses are carried out on-line. The detection limits of these analyzers are pushed downward to the ppt-range (parts per trillion), however the analyses are not more correct than the accuracy of the sampling system. A lot of attention has been put to the analyzers and the statistics to interpret the results but the sampling procedures has gained much less attention. This report aims to give guidance of the considerations to be made regarding sampling systems. Sampling is necessary since most analysis of interesting parameters cannot be carried out in- situ on-line in the steam cycle. Today's on-line instruments for pH, conductivity, silica etc. are designed to meet a water sample at a temperature of 10-30 deg C. This means that the sampling system has to extract a representative sample from the process, transport and cool it down to room temperature without changing the characteristics of the fluid. In the literature research work, standards and other reports can be found. Although giving similar recommendations in most aspects there are some discrepancies that may be confusing. This report covers all parts in the sampling system: Sample points and nozzles; Sample lines; Valves, regulating and on-off; Sample coolers; Temperature, pressure and flow rate control; Cooling water; and Water recovery. On-line analyzers connecting to the sampling system are not covered. This report aims to clarify what guidelines are most appropriate amongst the existing ones. The report should also give guidance to the design of the sampling system in order to achieve representative samples. In addition to this the report gives an overview of the fluid mechanics involved in sampling. The target group of this report is owners and operators of steam generators, vendors of power plant equipment, consultants working in

  5. Sampling art for ground-water monitoring wells in nuclide migration

    International Nuclear Information System (INIS)

    Liu Wenyuan; Tu Guorong; Dang Haijun; Wang Xuhui; Ke Changfeng

    2010-01-01

    Ground-Water sampling is one of the key parts in field nuclide migration. The objective of ground-water sampling program is to obtain samples that are representative of formation-quality water. In this paper, the ground-water sampling standards and the developments of sampling devices are reviewed. We also designed the sampling study projects which include the sampling methods, sampling parameters and the elementary devise of two types of ground-Water sampling devices. (authors)

  6. Filtration recovery of extracellular DNA from environmental water samples

    Science.gov (United States)

    qPCR methods are able to analyze DNA from microbes within hours of collecting water samples, providing the promptest notification and public awareness possible when unsafe pathogenic levels are reached. Health risk, however, may be overestimated by the presence of extracellular ...

  7. Determination of thiobencarb in water samples by gas ...

    African Journals Online (AJOL)

    Homogeneous liquid-liquid microextraction via flotation assistance (HLLME-FA) coupled with gas chromatography-flame ionization detection (GC-FID) was applied for the extraction and determination of thiobencarb in water samples. In this study, a special extraction cell was designed to facilitate collection of the ...

  8. Determination of lead at nanogram level in water samples by ...

    African Journals Online (AJOL)

    A novel method of chemistry applicable to the determination of trace lead in water samples based on the resonance light scattering (RLS) technique has been developed. In dilute phosphoric acid medium, in the presence of a large excess of I-, Pb(II) can form [PbI4]2-, which further reacts with tetrabutyl ammonium bromide ...

  9. preconcentration of uranium in water samples using dispersive

    African Journals Online (AJOL)

    B. S. Chandravanshi

    Atomic Energy Organization of Iran, P.O. Box 14395-836, Tehran, Iran. 2Department of ... A new liquid phase microextraction method based on the dispersion of an extraction solvent into aqueous phase ... optical emission spectrometry, Uranium, Water samples ..... The validation of the presented procedure was performed ...

  10. In situ sampling of interstitial water from lake sediments

    NARCIS (Netherlands)

    Brinkman, Albertus G.; van Raaphorst, Wim; Lijklema, Lambertus

    1982-01-01

    A sampler with a relatively high resolution has been developed, which allows interstitial water to be obtained from lake sediments at well defined depths, without serious disturbance of sediment structure. Oxidation effects are excluded. Sampling time is in the order of a day. Installation requires

  11. Ground-water sample collection and analysis plan for the ground-water surveillance project

    International Nuclear Information System (INIS)

    Bryce, R.W.; Evans, J.C.; Olsen, K.B.

    1991-12-01

    The Pacific Northwest Laboratory performs ground-water sampling activities at the US Department of Energy's (DOE's) Hanford Site in support of DOE's environmental surveillance responsibilities. The purpose of this document is to translate DOE's General Environmental Protection Program (DOE Order 5400.1) into a comprehensive ground-water sample collection and analysis plan for the Hanford Site. This sample collection and analysis plan sets forth the environmental surveillance objectives applicable to ground water, identifies the strategy for selecting sample collection locations, and lists the analyses to be performed to meet those objectives

  12. Algae viability over time in a ballast water sample

    Science.gov (United States)

    Gollasch, Stephan; David, Matej

    2018-03-01

    The biology of vessels' ballast water needs to be analysed for several reasons, one of these being performance tests of ballast water management systems. This analysis includes a viability assessment of phytoplankton. To overcome logistical problems to get algae sample processing gear on board of a vessel to document algae viability, samples may be transported to land-based laboratories. Concerns were raised how the storage conditions of the sample may impact algae viability over time and what the most appropriate storage conditions were. Here we answer these questions with a long-term algae viability study with daily sample analysis using Pulse-Amplitude Modulated (PAM) fluorometry. The sample was analysed over 79 days. We tested different storage conditions: fridge and room temperature with and without light. It seems that during the first two weeks of the experiment the viability remains almost unchanged with a slight downwards trend. In the continuing period, before the sample was split, a slightly stronger downwards viability trend was observed, which occurred at a similar rate towards the end of the experiment. After the sample was split, the strongest viability reduction was measured for the sample stored without light at room temperature. We concluded that the storage conditions, especially regarding temperature and light exposure, have a stronger impact on algae viability compared to the storage duration and that inappropriate storage conditions reduce algal viability. A sample storage time of up to two weeks in a dark and cool environment has little influence on the organism viability. This indicates that a two week time duration between sample taking on board a vessel and the viability measurement in a land-based laboratory may not be very critical.

  13. Water turbine system and method of operation

    Science.gov (United States)

    Costin, Daniel P.

    2010-06-15

    A system for providing electrical power from a current turbine is provided. The system includes a floatation device and a mooring. A water turbine structure is provided having an upper and lower portion wherein the lower portion includes a water fillable chamber. A plurality of cables are used to couple the system where a first cable couples the water turbine to the mooring and a second cable couples the floatation device to the first cable. The system is arranged to allow the turbine structure to be deployed and retrieved for service, repair, maintenance and redeployment.

  14. Collection and preparation of water samples for hydrogeochemical reconnaissance

    International Nuclear Information System (INIS)

    Baucom, E.I.; Ferguson, R.B.; Wallace, R.M.

    1977-01-01

    A method based on ion exchange and neutron activation analysis (NAA) was developed and field-tested to determine uranium over the range 0.02 to 10,000 ppb in natural water using a single procedure. Water samples are filtered in the field using a specially-designed one-liter filter apparatus pressurized to 40 psig with an inert gas. The filtered water is treated with a high purity, mixed cation-anion resin in the hydronium-hydroxide form. All ions are removed from solution under the strong driving force of the neutralization reaction. Anionic, cationic, and natural complexes of uranium can be concentrated with this method. Field tests showed greater than 95 percent recovery of 13 elements analyzed (including greater than 99 percent recovery of uranium) and greater than or equal to 90 percent recovery of 4 other elements. Uranium collected on the resin was quantitatively determined by NAA. Coefficient of variation for sampling plus analysis was less than 20 percent for samples containing more than 0.1 ppb uranium. Advantages of this method include: (1) wide dynamic range, (2) low detection limit for uranium (0.02 ppb), (3) high precision and accuracy, (4) relatively low cost, (5) high-yield recovery from low-level aqueous samples without risk of loss to containers, (6) decreased risk of significant sample contamination compared with other low-level methods, (7) production of stable samples suitable for retrievable storage, and(8) concentration of other ions that can be determined by NAA. This paper presents (1) background regarding development of procedures for sample collection and preparation, (2) results of development programs, (3) description of equipment and field procedures, and (4) preliminary conclusions regarding use of this technology for hydrogeochemical reconnaissance for uranium

  15. Determination of Cs-134 and Cs-137 rain water samples

    International Nuclear Information System (INIS)

    Lima, M.F.; Mazzilli, B.

    1988-01-01

    In order to setting an environmental monitoring program at IPEN, was developed a fast and simple methodology for concentration of Cs-134 and Cs-137 in rain water. This procedure consists in the precipitation of cesium and others cathions of its family (NH 4 + , K + and Rb + ) by ammonium molybdophosphate. The measures of the desintegration rates of Cs-134 and Cs-137 was done by gamma spectrometry in a Ge(Li) detector. After setting up the ideal experimental conditions, the procedure was used to analyze four samples of rain water. (author) [pt

  16. Hexagonal ice in pure water and biological NMR samples

    Energy Technology Data Exchange (ETDEWEB)

    Bauer, Thomas; Gath, Julia; Hunkeler, Andreas; Ernst, Matthias, E-mail: maer@ethz.ch [ETH Zurich, Physical Chemistry (Switzerland); Böckmann, Anja, E-mail: a.bockmann@ibcp.fr [UMR 5086 CNRS, Université de Lyon 1, Institut de Biologie et Chimie des Protéines (France); Meier, Beat H., E-mail: beme@ethz.ch [ETH Zurich, Physical Chemistry (Switzerland)

    2017-01-15

    Ice, in addition to “liquid” water and protein, is an important component of protein samples for NMR spectroscopy at subfreezing temperatures but it has rarely been observed spectroscopically in this context. We characterize its spectroscopic behavior in the temperature range from 100 to 273 K, and find that it behaves like pure water ice. The interference of magic-angle spinning (MAS) as well as rf multiple-pulse sequences with Bjerrum-defect motion greatly influences the ice spectra.

  17. Determination of Sr-90 in rain water samples

    International Nuclear Information System (INIS)

    Lima, M.F.; Cunha, I.I.L.

    1988-01-01

    A work that aim is to establish radiochemical method for the determination of Sr-90 in rain water samples has been studied, as a step in an environmental monitoring program of radioactive elements. The analysis includes the preconcentration of strontium diluted in a large volume sample by precipitation of strontium as carbonate, separation of strontium from interfering elements (calcium, barium and rare earths), separation of strontium from ytrium, precipitation of purified strontium and ytrium respectively as carbonate and oxalate, and counting of Sr-90 and Y-90 activities in a low background anticoincidence beta counter. (author) [pt

  18. Monolith Chromatography as Sample Preparation Step in Virome Studies of Water Samples.

    Science.gov (United States)

    Gutiérrez-Aguirre, Ion; Kutnjak, Denis; Rački, Nejc; Rupar, Matevž; Ravnikar, Maja

    2018-01-01

    Viruses exist in aquatic media and many of them use this media as transmission route. Next-generation sequencing (NGS) technologies have opened new doors in virus research, allowing also to reveal a hidden diversity of viral species in aquatic environments. Not surprisingly, many of the newly discovered viruses are found in environmental fresh and marine waters. One of the problems in virome research can be the low amount of viral nucleic acids present in the sample in contrast to the background ones (host, eukaryotic, prokaryotic, environmental). Therefore, virus enrichment prior to NGS is necessary in many cases. In water samples, an added problem resides in the low concentration of viruses typically present in aquatic media. Different concentration strategies have been used to overcome such limitations. CIM monoliths are a new generation of chromatographic supports that due to their particular structural characteristics are very efficient in concentration and purification of viruses. In this chapter, we describe the use of CIM monolithic chromatography for sample preparation step in NGS studies targeting viruses in fresh or marine water. The step-by-step protocol will include a case study where CIM concentration was used to study the virome of a wastewater sample using NGS.

  19. 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.

  20. An opacity-sampled treatment of water vapor

    Science.gov (United States)

    Alexander, David R.; Augason, Gordon C.; Johnson, Hollis R.

    1989-01-01

    Although the bands of H2O are strong in the spectra of cool stars and calculations have repeatedly demonstrated their significance as opacity sources, only approximate opacities are currently available, due both to the difficulty of accounting for the millions of lines involved and to the inadequacy of laboratory and theoretical data. To overcome these obstacles, a new treatment is presented, based upon a statistical representation of the water vapor spectrum derived from available laboratory data. This statistical spectrum of water vapor employs an exponential distribution of line strengths and random positions of lines whose overall properties are forced to reproduce the mean opacities observed in the laboratory. The resultant data set is then treated by the opacity-sampling method exactly as are all other lines, both molecular and atomic. Significant differences are found between the results of this improved treatment and the results obtained with previous treatments of water-vapor opacity.

  1. GROUND WATER SAMPLING OF VOCS IN THE WATER/CAPILLARY FRINGE AREA FOR VAPOR INTRUSION ASSESSMENT

    Science.gov (United States)

    Vapor intrusion has recently been considered a major pathway for increased indoor air contamination from certain volatile organic contaminants (VOCs). The recent Draft EPA Subsurface Vapor Intrusion Guidance Document states that ground water samples should be obtained from the u...

  2. Monitoring of fluoride in water samples using a smartphone

    Energy Technology Data Exchange (ETDEWEB)

    Levin, Saurabh [Akvo Foundation (Netherlands); Krishnan, Sunderrajan [INREM Foundation (India); Rajkumar, Samuel; Halery, Nischal; Balkunde, Pradeep [Akvo Foundation (Netherlands)

    2016-05-01

    In several parts of India, groundwater is the only reliable, year round source for drinking water. Prevention of fluorosis, a chronic disease resulting from excess intake of fluoride, requires the screening of all groundwater sources for fluoride in endemic areas. In this paper, the authors present a field deployable colorimetric analyzer based on an inexpensive smartphone embedded with digital camera for taking photograph of the colored solution as well as an easy-fit, and compact sample chamber (Akvo Caddisfly). Phones marketed by different smartphone makers were used. Commercially available zirconium xylenol orange reagent was used for determining fluoride concentration. A software program was developed to use with the phone for recording and analyzing the RGB color of the picture. Linear range for fluoride estimation was 0–2 mg l{sup −1}. Around 200 samples, which consisted of laboratory prepared as well as field samples collected from different locations in Karnataka, India, were tested with Akvo Caddisfly. The results showed a significant positive correlation between Ion Selective Electrode (ISE) method and Akvo Caddisfly (Phones A, B and C), with correlation coefficient ranging between 0.9952 and 1.000. In addition, there was no significant difference in the mean fluoride content values between ISE and Phone B and C except for Phone A. Thus the smartphone method is economical and suited for groundwater fluoride analysis in the field. - Highlights: • Fluoride is an inorganic pollutant in ground water, affecting human health. • A colorimetric method for measurement of fluoride in drinking water with smartphone • Measurement is by mixing water with zirconyl xylenol orange complex reagent. • Results are comparable with laboratory-based ion selective fluoride electrode method.

  3. Monitoring of fluoride in water samples using a smartphone

    International Nuclear Information System (INIS)

    Levin, Saurabh; Krishnan, Sunderrajan; Rajkumar, Samuel; Halery, Nischal; Balkunde, Pradeep

    2016-01-01

    In several parts of India, groundwater is the only reliable, year round source for drinking water. Prevention of fluorosis, a chronic disease resulting from excess intake of fluoride, requires the screening of all groundwater sources for fluoride in endemic areas. In this paper, the authors present a field deployable colorimetric analyzer based on an inexpensive smartphone embedded with digital camera for taking photograph of the colored solution as well as an easy-fit, and compact sample chamber (Akvo Caddisfly). Phones marketed by different smartphone makers were used. Commercially available zirconium xylenol orange reagent was used for determining fluoride concentration. A software program was developed to use with the phone for recording and analyzing the RGB color of the picture. Linear range for fluoride estimation was 0–2 mg l"−"1. Around 200 samples, which consisted of laboratory prepared as well as field samples collected from different locations in Karnataka, India, were tested with Akvo Caddisfly. The results showed a significant positive correlation between Ion Selective Electrode (ISE) method and Akvo Caddisfly (Phones A, B and C), with correlation coefficient ranging between 0.9952 and 1.000. In addition, there was no significant difference in the mean fluoride content values between ISE and Phone B and C except for Phone A. Thus the smartphone method is economical and suited for groundwater fluoride analysis in the field. - Highlights: • Fluoride is an inorganic pollutant in ground water, affecting human health. • A colorimetric method for measurement of fluoride in drinking water with smartphone • Measurement is by mixing water with zirconyl xylenol orange complex reagent. • Results are comparable with laboratory-based ion selective fluoride electrode method.

  4. Ion Chromatographic Analyses of Sea Waters, Brines and Related Samples

    Directory of Open Access Journals (Sweden)

    Nataša Gros

    2013-06-01

    Full Text Available This review focuses on the ion chromatographic methods for the analyses of natural waters with high ionic strength. At the beginning a natural diversity in ionic composition of waters is highlighted and terminology clarified. In continuation a brief overview of other review articles of potential interest is given. A review of ion chromatographic methods is organized in four sections. The first section comprises articles focused on the determination of ionic composition of water samples as completely as possible. The sections—Selected Anions, Selected Cations and Metals—follow. The most essential experimental conditions used in different methods are summarized in tables for a rapid comparison. Techniques encountered in the reviewed articles comprise: direct determinations of ions in untreated samples with ion- or ion-exclusion chromatography, or electrostatic ion chromatography; matrix elimination with column-switching; pre-concentration with a chelation ion chromatography and purge-and-trap pre-concentration. Different detection methods were used: non-suppressed conductometric or suppressed conductometric, direct spectrometric or spectrometric after a post-column derivetization, and inductively coupled plasma in combination with optical emission or mass spectrometry.

  5. Micellar electrokinetic chromatographic determination of triazine herbicides in water samples.

    Science.gov (United States)

    Li, Zhi; Zhang, Shuaihua; Yin, Xiaofang; Wang, Chun; Wang, Zhi

    2014-09-01

    Dispersive liquid-liquid microextraction combined with online sweeping preconcentration in micellar electrokinetic chromatography was developed for the simultaneous determination of five triazine herbicides (atrazine, simazine, propazine, prometon and simetryn) in water samples. Several experimental parameters affecting the extraction efficiencies such as the type and volume of both the extraction and dispersive solvents, the addition of salt to sample solution, the extraction time and the pH of the sample solution were investigated. Under optimum conditions, the linearity of the method was good in the range from 0.33 to 20 ng mL(-1) for simazine, propazine, atrazine and simetryn, and from 0.17 to 20 ng mL(-1) for prometon, respectively. The sensitivity enrichment factors were in the range from 1750 to 2100, depending on the compound. The limit of detection (S/N = 3) ranged from 0.05 to 0.10 ng mL(-1). The developed method was successfully applied to the analysis of the five triazines in river, ground and well waters. © The Author [2013]. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  6. Differences in microbial community composition between injection and production water samples of water flooding petroleum reservoirs

    Directory of Open Access Journals (Sweden)

    P. K. Gao

    2015-06-01

    Full Text Available Microbial communities in injected water are expected to have significant influence on those of reservoir strata in long-term water flooding petroleum reservoirs. To investigate the similarities and differences in microbial communities in injected water and reservoir strata, high-throughput sequencing of microbial partial 16S rRNA of the water samples collected from the wellhead and downhole of injection wells, and from production wells in a homogeneous sandstone reservoir and a heterogeneous conglomerate reservoir were performed. The results indicate that a small number of microbial populations are shared between the water samples from the injection and production wells in the sandstone reservoir, whereas a large number of microbial populations are shared in the conglomerate reservoir. The bacterial and archaeal communities in the reservoir strata have high concentrations, which are similar to those in the injected water. However, microbial population abundance exhibited large differences between the water samples from the injection and production wells. The number of shared populations reflects the influence of microbial communities in injected water on those in reservoir strata to some extent, and show strong association with the unique variation of reservoir environments.

  7. Nuclear power plants and the environment. Water samplings and releases

    International Nuclear Information System (INIS)

    Hartmann, Philippe; Bordet, Francois; Chevalier, Christian; Colin, Jean-Luc; Khalanski, Michel

    2013-01-01

    This voluminous and illustrated guide aims at giving detailed information on the nature of waters used by nuclear power plants and of releases, on how these samplings and controls are performed, on the associated risks for the environment and public health, and on how public is informed. After a general overview of these issues, a chapter addresses the protection of nature and biodiversity and the actions performed by EDF in this respect. The next chapter deals with public information. The next chapters discuss the water needs of a nuclear power plant, effluent releases and their impacts. Two chapters are dedicated to the monitoring and control of the environment, and to the various techniques of environmental metrology. Legal and regulatory aspects are then presented

  8. UMTRA Project water sampling and analysis plan, Salt Lake City, Utah. Revision 1

    International Nuclear Information System (INIS)

    1995-06-01

    This water sampling and analysis plan describes planned, routine ground water sampling activities at the US Department of Energy Uranium Mill Tailings Remedial Action Project site in Salt Lake City, Utah. This plan identifies and justifies sampling locations, analytical parameters, detection limits, and sampling frequencies for routine monitoring of ground water, sediments, and surface waters at monitoring stations on the site

  9. Multielement neutron activation analysis of underground water samples

    International Nuclear Information System (INIS)

    Kusaka, Yuzuru; Tsuji, Haruo; Fujimoto, Yuzo; Ishida, Keiko; Mamuro, Tetsuo.

    1980-01-01

    An instrumental neutron activation analysis by gamma-ray spectrometry with high resolution and large volume Ge (Li) detectors followed by data processing with an electronic computer was applied to the multielemental analysis to elucidate the chemical qualities of the underground water which has been widely used in the sake brewing industries in Mikage, Uozaki and Nishinomiya districts, called as miyamizu. The evaporated residues of the water samples were subjected to the neutron irradiations in reactor for 1 min at a thermal flux of 1.5 x 10 12 n.cm -2 .sec -1 and for 30 hrs at a thermal flux of 9.3 x 10 11 n.cm -2 .sec -1 or for 5 hrs at a thermal flux of 3.9 x 10 12 n.cm -2 .sec -1 . Thus, 11 elements in the former short irradiation and 38 elements in the latter two kinds of long irradiation can be analyzed. Conventional chemical analysis including atomic absorption method and others are also applied on the same samples, and putting the all results together, some considerations concerning the geochemical meaning of the analytical values are made. (author)

  10. Determination of 210Pb and 210Po in water samples

    International Nuclear Information System (INIS)

    Ayranov, M.; Tosheva, Z.; Kies, A.

    2004-01-01

    Lead-210 and Polonium-210 are naturally occurring members of the Uranium-238 decay series. They could be found in various environmental samples, such as groundwater, fish and shellfish, contributing an important component of the human natural radiation background. For this reason the development of a fast, reproducible and sensitive method for determination of 210 Pb and 210 Po is of a great concern. The aims of our study were to adopt procedures for radiochemical separation of these radionuclides and radioanalytical methods for their determination. The combination of electrochemical deposition, co-precipitation and extraction chromatography gives the opportunity for fast and effective radiochemical separation of the analytes. Polonium was spontaneously plated on copper disk from the stock solution. Lead was co-precipitated with Fe(OH) 3 and further purified by extraction chromatography on Sr Spec columns. Alpha spectra of polonium were collected on Canberra PIPS detectors with 900 mm 2 active surface. The activities of lead were determined by LSC (Gardian Wallac Oy). The minimum detectable activities for sample size 1000 mL and chemical yield of 88 % for the polonium and 85 % for the lead are presented. The proposed method proved to be fast, accurate and reproducible for routine determination of lead and polonium in environmental water samples. (authors)

  11. Fluorescent determination of graphene quantum dots in water samples

    Energy Technology Data Exchange (ETDEWEB)

    Benítez-Martínez, Sandra; Valcárcel, Miguel, E-mail: qa1meobj@uco.es

    2015-10-08

    This work presents a simple, fast and sensitive method for the preconcentration and quantification of graphene quantum dots (GQDs) in aqueous samples. GQDs are considered an object of analysis (analyte) not an analytical tool which is the most frequent situation in Analytical Nanoscience and Nanotechnology. This approach is based on the preconcentration of graphene quantum dots on an anion exchange sorbent by solid phase extraction and their subsequent elution prior fluorimetric analysis of the solution containing graphene quantum dots. Parameters of the extraction procedure such as sample volume, type of solvent, sample pH, sample flow rate and elution conditions were investigated in order to achieve extraction efficiency. The limits of detection and quantification were 7.5 μg L{sup −1} and 25 μg L{sup −1}, respectively. The precision for 200 μg L{sup −1}, expressed as %RSD, was 2.8%. Recoveries percentages between 86.9 and 103.9% were obtained for two different concentration levels. Interferences from other nanoparticles were studied and no significant changes were observed at the concentration levels tested. Consequently, the optimized procedure has great potential to be applied to the determination of graphene quantum dots at trace levels in drinking and environmental waters. - Highlights: • Development of a novel and simple method for determination of graphene quantum dots. • Preconcentration of graphene quantum dots by solid phase extraction. • Fluorescence spectroscopy allows fast measurements. • High sensitivity and great reproducibility are achieved.

  12. Liquid Water from First Principles: Validation of Different Sampling Approaches

    Energy Technology Data Exchange (ETDEWEB)

    Mundy, C J; Kuo, W; Siepmann, J; McGrath, M J; Vondevondele, J; Sprik, M; Hutter, J; Parrinello, M; Mohamed, F; Krack, M; Chen, B; Klein, M

    2004-05-20

    A series of first principles molecular dynamics and Monte Carlo simulations were carried out for liquid water to assess the validity and reproducibility of different sampling approaches. These simulations include Car-Parrinello molecular dynamics simulations using the program CPMD with different values of the fictitious electron mass in the microcanonical and canonical ensembles, Born-Oppenheimer molecular dynamics using the programs CPMD and CP2K in the microcanonical ensemble, and Metropolis Monte Carlo using CP2K in the canonical ensemble. With the exception of one simulation for 128 water molecules, all other simulations were carried out for systems consisting of 64 molecules. It is found that the structural and thermodynamic properties of these simulations are in excellent agreement with each other as long as adiabatic sampling is maintained in the Car-Parrinello molecular dynamics simulations either by choosing a sufficiently small fictitious mass in the microcanonical ensemble or by Nos{acute e}-Hoover thermostats in the canonical ensemble. Using the Becke-Lee-Yang-Parr exchange and correlation energy functionals and norm-conserving Troullier-Martins or Goedecker-Teter-Hutter pseudopotentials, simulations at a fixed density of 1.0 g/cm{sup 3} and a temperature close to 315 K yield a height of the first peak in the oxygen-oxygen radial distribution function of about 3.0, a classical constant-volume heat capacity of about 70 J K{sup -1} mol{sup -1}, and a self-diffusion constant of about 0.1 Angstroms{sup 2}/ps.

  13. Determination of trihalomethanes in water samples: A review

    Energy Technology Data Exchange (ETDEWEB)

    Perez Pavon, Jose Luis [Departamento de Quimica Analitica, Nutricion y Bromatologia, Facultad de Ciencias Quimicas, Universidad de Salamanca, 37008 Salamanca (Spain)], E-mail: jlpp@usal.es; Herrero Martin, Sara; Garcia Pinto, Carmelo; Moreno Cordero, Bernardo [Departamento de Quimica Analitica, Nutricion y Bromatologia, Facultad de Ciencias Quimicas, Universidad de Salamanca, 37008 Salamanca (Spain)

    2008-11-23

    This article reviews the most recent literature addressing the analytical methods applied for trihalomethanes (THMs) determination in water samples. This analysis is usually performed with gas chromatography (GC) combined with a preconcentration step. The detectors most widely used in this type of analyses are mass spectrometers (MS) and electron capture detectors (ECD). Here, we review the analytical characteristics, the time required for analysis, and the simplicity of the optimised methods. The main difference between these methods lies in the sample pretreatment step; therefore, special emphasis is placed on this aspect. The techniques covered are direct aqueous injection (DAI), liquid-liquid extraction (LLE), headspace (HS), and membrane-based techniques. We also review the main chromatographic columns employed and consider novel aspects of chromatographic analysis, such as the use of fast gas chromatography (FGC). Concerning the detection step, besides the common techniques, the use of uncommon detectors such as fluorescence detector, pulsed discharge photoionization detector (PDPID), dry electrolytic conductivity detector (DELCD), atomic emission detector (AED) and inductively coupled plasma-mass spectrometry (ICP-MS) for this type of analysis is described.

  14. Sampling and analysis for radon-222 dissolved in ground water and surface water

    Science.gov (United States)

    DeWayne, Cecil L.; Gesell, T.F.

    1992-01-01

    Radon-222 is a naturally occurring radioactive gas in the uranium-238 decay series that has traditionally been called, simply, radon. The lung cancer risks associated with the inhalation of radon decay products have been well documented by epidemiological studies on populations of uranium miners. The realization that radon is a public health hazard has raised the need for sampling and analytical guidelines for field personnel. Several sampling and analytical methods are being used to document radon concentrations in ground water and surface water worldwide but no convenient, single set of guidelines is available. Three different sampling and analytical methods - bubbler, liquid scintillation, and field screening - are discussed in this paper. The bubbler and liquid scintillation methods have high accuracy and precision, and small analytical method detection limits of 0.2 and 10 pCi/l (picocuries per liter), respectively. The field screening method generally is used as a qualitative reconnaissance tool.

  15. Sampling trace organic compounds in water: a comparison of a continuous active sampler to continuous passive and discrete sampling methods.

    Science.gov (United States)

    Coes, Alissa L; Paretti, Nicholas V; Foreman, William T; Iverson, Jana L; Alvarez, David A

    2014-03-01

    A continuous active sampling method was compared to continuous passive and discrete sampling methods for the sampling of trace organic compounds (TOCs) in water. Results from each method are compared and contrasted in order to provide information for future investigators to use while selecting appropriate sampling methods for their research. The continuous low-level aquatic monitoring (CLAM) sampler (C.I.Agent® Storm-Water Solutions) is a submersible, low flow-rate sampler, that continuously draws water through solid-phase extraction media. CLAM samplers were deployed at two wastewater-dominated stream field sites in conjunction with the deployment of polar organic chemical integrative samplers (POCIS) and the collection of discrete (grab) water samples. All samples were analyzed for a suite of 69 TOCs. The CLAM and POCIS samples represent time-integrated samples that accumulate the TOCs present in the water over the deployment period (19-23 h for CLAM and 29 days for POCIS); the discrete samples represent only the TOCs present in the water at the time and place of sampling. Non-metric multi-dimensional scaling and cluster analysis were used to examine patterns in both TOC detections and relative concentrations between the three sampling methods. A greater number of TOCs were detected in the CLAM samples than in corresponding discrete and POCIS samples, but TOC concentrations in the CLAM samples were significantly lower than in the discrete and (or) POCIS samples. Thirteen TOCs of varying polarity were detected by all of the three methods. TOC detections and concentrations obtained by the three sampling methods, however, are dependent on multiple factors. This study found that stream discharge, constituent loading, and compound type all affected TOC concentrations detected by each method. In addition, TOC detections and concentrations were affected by the reporting limits, bias, recovery, and performance of each method. Published by Elsevier B.V.

  16. Sampling trace organic compounds in water: a comparison of a continuous active sampler to continuous passive and discrete sampling methods

    Science.gov (United States)

    Coes, Alissa L.; Paretti, Nicholas V.; Foreman, William T.; Iverson, Jana L.; Alvarez, David A.

    2014-01-01

    A continuous active sampling method was compared to continuous passive and discrete sampling methods for the sampling of trace organic compounds (TOCs) in water. Results from each method are compared and contrasted in order to provide information for future investigators to use while selecting appropriate sampling methods for their research. The continuous low-level aquatic monitoring (CLAM) sampler (C.I.Agent® Storm-Water Solutions) is a submersible, low flow-rate sampler, that continuously draws water through solid-phase extraction media. CLAM samplers were deployed at two wastewater-dominated stream field sites in conjunction with the deployment of polar organic chemical integrative samplers (POCIS) and the collection of discrete (grab) water samples. All samples were analyzed for a suite of 69 TOCs. The CLAM and POCIS samples represent time-integrated samples that accumulate the TOCs present in the water over the deployment period (19–23 h for CLAM and 29 days for POCIS); the discrete samples represent only the TOCs present in the water at the time and place of sampling. Non-metric multi-dimensional scaling and cluster analysis were used to examine patterns in both TOC detections and relative concentrations between the three sampling methods. A greater number of TOCs were detected in the CLAM samples than in corresponding discrete and POCIS samples, but TOC concentrations in the CLAM samples were significantly lower than in the discrete and (or) POCIS samples. Thirteen TOCs of varying polarity were detected by all of the three methods. TOC detections and concentrations obtained by the three sampling methods, however, are dependent on multiple factors. This study found that stream discharge, constituent loading, and compound type all affected TOC concentrations detected by each method. In addition, TOC detections and concentrations were affected by the reporting limits, bias, recovery, and performance of each method.

  17. Assessment of Sr-90 in water samples: precision and accuracy

    Energy Technology Data Exchange (ETDEWEB)

    Nisti, Marcelo B.; Saueia, Cátia H.R.; Castilho, Bruna; Mazzilli, Barbara P., E-mail: mbnisti@ipen.br, E-mail: chsaueia@ipen.br, E-mail: bcastilho@ipen.br, E-mail: mazzilli@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2017-11-01

    The study of artificial radionuclides dispersion into the environment is very important to control the nuclear waste discharges, nuclear accidents and nuclear weapons testing. The accidents in Fukushima Daiichi Nuclear Power Plant and Chernobyl Nuclear Power Plant, released several radionuclides in the environment by aerial deposition and liquid discharge, with various level of radioactivity. The {sup 90}Sr was one of the elements released into the environment. The {sup 90}Sr is produced by nuclear fission with a physical half-life of 28.79 years with decay energy of 0.546 MeV. The aims of this study are to evaluate the precision and accuracy of three methodologies for the determination of {sup 90}Sr in water samples: Cerenkov, LSC direct method and with radiochemical separation. The performance of the methodologies was evaluated by using two scintillation counters (Quantulus and Hidex). The parameters Minimum Detectable Activity (MDA) and Figure Of Merit (FOM) were determined for each method, the precision and accuracy were checked using {sup 90}Sr standard solutions. (author)

  18. Verification of spectrophotometric method for nitrate analysis in water samples

    Science.gov (United States)

    Kurniawati, Puji; Gusrianti, Reny; Dwisiwi, Bledug Bernanti; Purbaningtias, Tri Esti; Wiyantoko, Bayu

    2017-12-01

    The aim of this research was to verify the spectrophotometric method to analyze nitrate in water samples using APHA 2012 Section 4500 NO3-B method. The verification parameters used were: linearity, method detection limit, level of quantitation, level of linearity, accuracy and precision. Linearity was obtained by using 0 to 50 mg/L nitrate standard solution and the correlation coefficient of standard calibration linear regression equation was 0.9981. The method detection limit (MDL) was defined as 0,1294 mg/L and limit of quantitation (LOQ) was 0,4117 mg/L. The result of a level of linearity (LOL) was 50 mg/L and nitrate concentration 10 to 50 mg/L was linear with a level of confidence was 99%. The accuracy was determined through recovery value was 109.1907%. The precision value was observed using % relative standard deviation (%RSD) from repeatability and its result was 1.0886%. The tested performance criteria showed that the methodology was verified under the laboratory conditions.

  19. Legionella saoudiensis sp. nov., isolated from a sewage water sample.

    Science.gov (United States)

    Bajrai, Leena Hussein; Azhar, Esam Ibraheem; Yasir, Muhammad; Jardot, Priscilla; Barrassi, Lina; Raoult, Didier; La Scola, Bernard; Pagnier, Isabelle

    2016-11-01

    A Gram-stain-negative, bacilli-shaped bacterial strain, LS-1T, was isolated from a sewage water sample collected in Jeddah, Saudi Arabia. The taxonomic position of strain LS-1T was investigated using a polyphasic taxonomic approach. Phylogenetic analysis based on 16S rRNA gene sequences and those of four other genes indicated that strain LS-1T belongs to the genus Legionella in the family Legionellaceae. Regarding the 16S rRNA gene, the most closely related species are Legionella rowbothamii LLAP-6T (98.6 %) and Legionella lytica L2T (98.5 %). The mip gene sequence of strain LS-1T showed 94 % sequence similarity with that of L. lytica L2T and 93 % similarity with that of L. rowbothamii LLAP-6T. Strain LS-1T grew optimally at a temperature of 32 °C on a buffered charcoal yeast extract (BCYE) agar plate in a 5 % CO2 atmosphere and had a flagellum. The combined phylogenetic, phenotypic and genomic sequence data suggest that strain LS-1T represents a novel species of the genus Legionella, for which the name Legionella saoudiensis sp. nov. is proposed. The type strain is LS-1T (=DSM 101682T=CSUR P2101T).

  20. Methods to maximise recovery of environmental DNA from water samples.

    Directory of Open Access Journals (Sweden)

    Rheyda Hinlo

    Full Text Available The environmental DNA (eDNA method is a detection technique that is rapidly gaining credibility as a sensitive tool useful in the surveillance and monitoring of invasive and threatened species. Because eDNA analysis often deals with small quantities of short and degraded DNA fragments, methods that maximize eDNA recovery are required to increase detectability. In this study, we performed experiments at different stages of the eDNA analysis to show which combinations of methods give the best recovery rate for eDNA. Using Oriental weatherloach (Misgurnus anguillicaudatus as a study species, we show that various combinations of DNA capture, preservation and extraction methods can significantly affect DNA yield. Filtration using cellulose nitrate filter paper preserved in ethanol or stored in a -20°C freezer and extracted with the Qiagen DNeasy kit outperformed other combinations in terms of cost and efficiency of DNA recovery. Our results support the recommendation to filter water samples within 24hours but if this is not possible, our results suggest that refrigeration may be a better option than freezing for short-term storage (i.e., 3-5 days. This information is useful in designing eDNA detection of low-density invasive or threatened species, where small variations in DNA recovery can signify the difference between detection success or failure.

  1. Assessment of Sr-90 in water samples: precision and accuracy

    International Nuclear Information System (INIS)

    Nisti, Marcelo B.; Saueia, Cátia H.R.; Castilho, Bruna; Mazzilli, Barbara P.

    2017-01-01

    The study of artificial radionuclides dispersion into the environment is very important to control the nuclear waste discharges, nuclear accidents and nuclear weapons testing. The accidents in Fukushima Daiichi Nuclear Power Plant and Chernobyl Nuclear Power Plant, released several radionuclides in the environment by aerial deposition and liquid discharge, with various level of radioactivity. The 90 Sr was one of the elements released into the environment. The 90 Sr is produced by nuclear fission with a physical half-life of 28.79 years with decay energy of 0.546 MeV. The aims of this study are to evaluate the precision and accuracy of three methodologies for the determination of 90 Sr in water samples: Cerenkov, LSC direct method and with radiochemical separation. The performance of the methodologies was evaluated by using two scintillation counters (Quantulus and Hidex). The parameters Minimum Detectable Activity (MDA) and Figure Of Merit (FOM) were determined for each method, the precision and accuracy were checked using 90 Sr standard solutions. (author)

  2. chemical and microbiological assessment of surface water samples

    African Journals Online (AJOL)

    PROF EKWUEME

    concentrations and bacteriological content. Evaluation of the results ... and Aninri local government areas of Enugu state. Surface water ... surface water bodies are prone to impacts from ... Coal Measures (Akamigbo, 1987). The geologic map ...

  3. Propagation of errors from a null balance terahertz reflectometer to a sample's relative water content

    International Nuclear Information System (INIS)

    Hadjiloucas, S; Walker, G C; Bowen, J W; Zafiropoulos, A

    2009-01-01

    The THz water content index of a sample is defined and advantages in using such metric in estimating a sample's relative water content are discussed. The errors from reflectance measurements performed at two different THz frequencies using a quasi-optical null-balance reflectometer are propagated to the errors in estimating the sample water content index.

  4. Bacteriological analysis of well water samples in Sagamu | Idowu ...

    African Journals Online (AJOL)

    Majority of the population in semi-urban and urban areas of Nigeria depend on wells as their source of water supply. Due to increasing cases of water-borne diseases in recent times, this study was carried out to examine the microbial quality of well water in Sagamu, Nigeria as a way of safeguarding public health against ...

  5. Real-time analysis of water movement in plant sample

    International Nuclear Information System (INIS)

    Yokota, Harumi; Furukawa, Jun; Tanoi, Keitaro

    2000-01-01

    To know the effect of drought stress on two cultivars of cowpea, drought tolerant (DT) and drought sensitive (DS), and to estimate vanadium treatment on plant activity, we performed real time 18 F labeled water uptake measurement by PETIS. Fluoride-18 was produced by bombarding a cubic ice target with 50 MeV protons using TIARA AVF cyclotron. Then 18 F labeled water was applied to investigate water movement in a cowpea plant. Real time water uptake manner could be monitored by PETIS. After the analysis by PETIS, we also measured the distribution of 18 F in a whole plant by BAS. When a cowpea plant was treated with drought stress, there was a difference in water uptake manner between DT and DS cultivar. When a cowpea plant was treated with V for 20 hours before the water uptake experiment, the total amount of 18 F labeled water absorption was found to be drastically decreased. (author)

  6. Real-time analysis of water movement in plant sample

    Energy Technology Data Exchange (ETDEWEB)

    Yokota, Harumi; Furukawa, Jun; Tanoi, Keitaro [Graduate School, Tokyo Univ. (Japan)

    2000-07-01

    To know the effect of drought stress on two cultivars of cowpea, drought tolerant (DT) and drought sensitive (DS), and to estimate vanadium treatment on plant activity, we performed real time{sup 18}F labeled water uptake measurement by PETIS. Fluoride-18 was produced by bombarding a cubic ice target with 50 MeV protons using TIARA AVF cyclotron. Then {sup 18}F labeled water was applied to investigate water movement in a cowpea plant. Real time water uptake manner could be monitored by PETIS. After the analysis by PETIS, we also measured the distribution of {sup 18}F in a whole plant by BAS. When a cowpea plant was treated with drought stress, there was a difference in water uptake manner between DT and DS cultivar. When a cowpea plant was treated with V for 20 hours before the water uptake experiment, the total amount of {sup 18}F labeled water absorption was found to be drastically decreased. (author)

  7. Development of analytical techniques for water and environmental samples (2)

    Energy Technology Data Exchange (ETDEWEB)

    Eum, Chul Hun; Jeon, Chi Wan; Jung, Kang Sup; Song, Kyung Sun; Kim, Sang Yeon [Korea Institute of Geology Mining and Materials, Taejon (Korea)

    1998-12-01

    The purpose of this study is to develop new analytical methods with good detection limit for toxic inorganic and organic compounds. The analyses of CN, organic acids, particulate materials in environmental samples have been done using several methods such as Ion Chromatography, SPE, SPME, GC/MS, GC/FID, SPLITT (split-flow thin cell fractionation) during the second year of this project. Advantage and disadvantage of several distillation method (by KS, JIS, EPA) for CN analysis in wastewater were investigated. As the results, we proposed new distillation apparatus for CN analysis, which was proved to be simpler, faster and to get better recovery than conventional apparatus. And ion chromatograph/pulsed amperometric detector (IC/PAD) system instead of colorimetry for CN detection was setup to solve matrix interference. And SPE(solid phase extraction) and SPME (solid phase micro extraction) as liquid-solid extraction technique were applied to the analysis of phenols in wastewater. Optimum experimental conditions and factors influencing analytical results were determined. From these results, It could be concluded that C{sub 18} cartridge and polystyrene-divinylbenzene disk in SPE method, polyacrylate fiber in SPME were proper solid phase adsorbent for phenol. Optimum conditions to analyze phenol derivatives simultaneously were established. Also, Continuous SPLITT (Split-flow thin cell) Fractionation (CSF) is a new preparative separation technique that is useful for fractionation of particulate and macromolecular materials. CSF is carried out in a thin ribbon-like channel equipped with two splitters at both inlet and outlet of the channel. In this work, we set up a new CSF system, and tested using polystyrene latex standard particles. And then we fractionated particles contained in air and underground water based on their sedimentation coefficients using CSF. (author). 27 refs., 13 tabs., 31 figs.

  8. Evaluation of storage and filtration protocols for alpine/subalpine lake water quality samples

    Science.gov (United States)

    John L. Korfmacher; Robert C. Musselman

    2007-01-01

    Many government agencies and other organizations sample natural alpine and subalpine surface waters using varying protocols for sample storage and filtration. Simplification of protocols would be beneficial if it could be shown that sample quality is unaffected. In this study, samples collected from low ionic strength waters in alpine and subalpine lake inlets...

  9. Levels of Cadmium in Soil, Sediment and Water Samples from ...

    African Journals Online (AJOL)

    cce

    The agricultural application of phosphate fertilizers represents a direct ... The samples were put into clean plastic containers and sealed. The plastic ... dried samples were ground and homogenized in a porcelain mortar, sieved to 40 mesh size.

  10. Detection of Cryptosporidium and Cyclospora Oocysts from Environmental Water for Drinking and Recreational Activities in Sarawak, Malaysia.

    Science.gov (United States)

    Bilung, Lesley Maurice; Tahar, Ahmad Syatir; Yunos, Nur Emyliana; Apun, Kasing; Lim, Yvonne Ai-Lian; Nillian, Elexson; Hashim, Hashimatul Fatma

    2017-01-01

    Cryptosporidiosis and cyclosporiasis are caused by waterborne coccidian protozoan parasites of the genera Cryptosporidium and Cyclospora, respectively. This study was conducted to detect Cryptosporidium and Cyclospora oocysts from environmental water abstracted by drinking water treatment plants and recreational activities in Sarawak, Malaysia. Water samples (12 each) were collected from Sungai Sarawak Kanan in Bau and Sungai Sarawak Kiri in Batu Kitang, respectively. In addition, 6 water samples each were collected from Ranchan Recreational Park and UNIMAS Lake at Universiti Malaysia Sarawak, Kota Samarahan, respectively. Water physicochemical parameters were also recorded. All samples were concentrated by the iron sulfate flocculation method followed by the sucrose floatation technique. Cryptosporidium and Cyclospora were detected by modified Ziehl-Neelsen technique. Correlation of the parasites distribution with water physicochemical parameters was analysed using bivariate Pearson correlation. Based on the 24 total samples of environmental water abstracted by drinking water treatment plants, all the samples (24/24; 100%) were positive with Cryptosporidium , and only 2 samples (2/24; 8.33%) were positive with Cyclospora . Based on the 12 total samples of water for recreational activities, 4 samples (4/12; 33%) were positive with Cryptosporidium , while 2 samples (2/12; 17%) were positive with Cyclospora . Cryptosporidium oocysts were negatively correlated with dissolved oxygen (DO).

  11. Tritium concentrations in environmental water and food samples collected around the vicinity of the PNPP-1

    International Nuclear Information System (INIS)

    Garcia, T.Y.; Enriquez, S.O.; Duran, E.B.

    1986-01-01

    The natural radioactivity levels of tritium in environmental samples collected around the vicinity and more distant environment of the first Philippine Nuclear Power Plant (PNPP-1) in Bataan were assessed. The samples analyzed consisted of water samples such as seawater, freshwater, drinking water, groundwater and rainwater; and food samples such as cereals, vegetables, fruits; meat, milk fish and crustaceans. Tritium concentrations in water samples were determined by distillation and liquid scintillation counting techniques. The food samples were analyzed for tissue-free water tritium by the freezing-drying method followed by liquid scintillation counting techniques. (Auth.) 13 refs

  12. Evaluation Of Sachet Water Samples In Owerri Metropolis | Nwosu ...

    African Journals Online (AJOL)

    Other surveys revealed that 12 brands had fake manufactures' address, 2 brands had NAFDAC registration number while 3 brands had genuine manufacturers' address on them. It was discovered that the producers packaged the water from their water source without any form of treatment or analysis on it. Key words: ...

  13. Soluble and insoluble pollutants in fog and rime water samples

    Czech Academy of Sciences Publication Activity Database

    Fišák, Jaroslav; Stoyanova, V.; Chaloupecký, Pavel; Řezáčová, Daniela; Tsacheva, Ts.; Kupenova, T.; Marinov, M.

    2009-01-01

    Roč. 4, Sp. Iss. 2 (2009), S123-S130 ISSN 1801-5395 R&D Projects: GA ČR GA205/09/1918; GA AV ČR 1QS200420562 Institutional research plan: CEZ:AV0Z30420517 Keywords : fog water * rime water * pollutant concentration Subject RIV: DG - Athmosphere Sciences, Meteorology

  14. PARASITIC CONTAMINATION OF WELLS DRINKING WATER IN MAZANDARAN PROVINCE

    Directory of Open Access Journals (Sweden)

    Z. Yousefi ، H. Ziaei hezarjaribi ، A. A. Enayati ، R. A. Mohammadpoor

    2009-10-01

    Full Text Available There is a direct relation between the prevalence of some parasitic diseases and the presence of those etiologic agents in water. The purpose of this research was to determine the contamination rate of wells drinking water to parasites in Mazandaran province in the north of Iran. 989 water samples were randomly taken based on the population of towns and number of health centers from 12 cities of Mazandaran province and transferred to the laboratory in sterile containers. Water samples were then filtered and analyzed according to the World Health Organization guidelines. Direct method and Gram staining procedure were used to identify the parasites. If cryptosporidium was seen, floatation (sheather’s sugar and modified Ziehl-Neelsen staining method were performed. Parasites count was undertaken using McMaster counting slide (0.3 mL. 197 out of 989 water samples were contaminated with different parasites. From 197 contaminated samples, 20 different types of parasites were separated of which 53 (26.9% were pathogenic, 100 (50.8% non pathogenic, and 44 non-infective stages of parasites. Distance between wells and sources of contamination, type of water distribution systems, city and chlorination status had significantly statistical relationship with contamination prevalence (p<0.001. According to the results and considering the direct correlation between safe water and human health, proper implementation of providing hygienic drinking water should be enforced.

  15. Storm Water Sampling Data 11-16-17.

    Energy Technology Data Exchange (ETDEWEB)

    Holland, Robert C. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2017-12-01

    In the California Industrial General Permit (IGP) 2014-0057-DWQ for storm water monitoring, effective July 1, 2015, there are 21 contaminants that have been assigned NAL (Numeric Action Level) values, both annual and instantaneous.

  16. Mutagenicity of drinking water sampled from the Yangtze River and Hanshui River (Wuhan section) and correlations with water quality parameters.

    Science.gov (United States)

    Lv, Xuemin; Lu, Yi; Yang, Xiaoming; Dong, Xiaorong; Ma, Kunpeng; Xiao, Sanhua; Wang, Yazhou; Tang, Fei

    2015-03-31

    A total of 54 water samples were collected during three different hydrologic periods (level period, wet period, and dry period) from Plant A and Plant B (a source for Yangtze River and Hanshui River water, respectively), and several water parameters, such as chemical oxygen demand (COD), turbidity, and total organic carbon (TOC), were simultaneously analyzed. The mutagenicity of the water samples was evaluated using the Ames test with Salmonella typhimurium strains TA98 and TA100. According to the results, the organic compounds in the water were largely frame-shift mutagens, as positive results were found for most of the tests using TA98. All of the finished water samples exhibited stronger mutagenicity than the relative raw and distribution water samples, with water samples collected from Plant B presenting stronger mutagenic strength than those from Plant A. The finished water samples from Plant A displayed a seasonal-dependent variation. Water parameters including COD (r = 0.599, P = 0.009), TOC (r = 0.681, P = 0.02), UV254 (r = 0.711, P = 0.001), and total nitrogen (r = 0.570, P = 0.014) exhibited good correlations with mutagenicity (TA98), at 2.0 L/plate, which bolsters the argument of the importance of using mutagenicity as a new parameter to assess the quality of drinking water.

  17. UMTRA Project water sampling and analysis plan: Canonsburg and Burrell, Pennsylvania

    International Nuclear Information System (INIS)

    1994-03-01

    Surface remedial action was completed at the Canonsburg and Burrell UMTRA Project sites in southwestern Pennsylvania in 1985 and 1987, respectively. Results of 1993 water sampling indicate ground water flow conditions and ground water quality at both sites have remained relatively consistent with time. Uranium concentrations in ground water continue to exceed the maximum concentration limit (MCL) at the Canonsburg site; no MCLs are exceeded in ground water at the Burrell site. Surface water quality shows no evidence of impact from the sites

  18. Total and inorganic arsenic in fish samples from Norwegian waters

    DEFF Research Database (Denmark)

    Julshamn, K.; Nilsen, B. M.; Frantzen, S.

    2012-01-01

    The contents of total arsenic and inorganic arsenic were determined in fillet samples of Northeast Arctic cod, herring, mackerel, Greenland halibut, tusk, saithe and Atlantic halibut. In total, 923 individual fish samples were analysed. The fish were mostly caught in the open sea off the coast......-assisted dissolution of the samples. The concentrations found for total arsenic varied greatly between fish species, and ranged from 0.3 to 110 mg kg–1 wet weight. For inorganic arsenic, the concentrations found were very low (...

  19. Mass transfer of H2O between petroleum and water: implications for oil field water sample quality

    International Nuclear Information System (INIS)

    McCartney, R.A.; Ostvold, T.

    2005-01-01

    Water mass transfer can occur between water and petroleum during changes in pressure and temperature. This process can result in the dilution or concentration of dissolved ions in the water phase of oil field petroleum-water samples. In this study, PVT simulations were undertaken for 4 petroleum-water systems covering a range of reservoir conditions (80-185 o C; 300-1000 bar) and a range of water-petroleum mixtures (volume ratios of 1:1000-300:1000) to quantify the extent of H 2 O mass transfer as a result of pressure and temperature changes. Conditions were selected to be relevant to different types of oil field water sample (i.e. surface, downhole and core samples). The main variables determining the extent of dilution and concentration were found to be: (a) reservoir pressure and temperature, (b) pressure and temperature of separation of water and petroleum, (c) petroleum composition, and (d) petroleum:water ratio (PWR). The results showed that significant dilution and concentration of water samples could occur, particularly at high PWR. It was not possible to establish simple guidelines for identifying good and poor quality samples due to the interplay of the above variables. Sample quality is best investigated using PVT software of the type used in this study. (author)

  20. LTRM Water Quality Sampling Strata, UMRS La Grange Reach

    Data.gov (United States)

    Department of the Interior — The data set includes delineation of sampling strata for the six study reaches of the UMRR Program’s LTRM element. Separate strata coverages exist for each of the...

  1. Fiscal 1980 Sunshine Project research report. R and D on preventive technology of scale deposition derived from hot water; 1980 nendo chinetsu nessui kara no scale fuchaku wo boshisuru gijutsu no kenkyu kaihatsu seika hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1981-03-31

    This report summarizes the fiscal 1980 research result on preventive technology of scale deposition derived from hot water. Hot water of Nigori-Gawa, Hokkaido forms CaCO{sub 3} scale just after releasing into ambient air, and scale composed of amorphous silica and calcite at 60 degrees C or less, reaching a peak around pH 8. Deposition increases with a decrease in flow velocity and temperature. Polymerized silica removal experiment was made using Otake hot water and a floatation separator of 1 T/H. No cation and kerosene, and additional 6A-1 (coconut amine) and NS-18 (amine T) were effective for floatation separation. Continuous operation of the floatation separator of 50 T/H and a sludge recycling equipment was carried out as test for practical use. It was confirmed that addition of amine system floatation agent to hot water of 80 degrees C and pH 5 with polymerized silica of 20ppm is effective for reduction of polymerized silica in treatment water to 5ppm or less. The treated water was reinjected into Otake No.6 reinjection well. The sludge recycling equipment was tested for recycling floatation sludge separated, resulting in achievement of an expected target. (NEDO)

  2. Difficulties in obtaining representative samples for compliance with the Ballast Water Management Convention

    Digital Repository Service at National Institute of Oceanography (India)

    Carney, K.J; Basurko, O.C; Pazouki, K.; Marsham, S.; Delany, J; Desai, D.V.; Anil, A.C; Mesbahi, E.

    water, the shape, size and number of ballast tanks and the heterogeneous distribution of organisms within tanks. These factors hinder efforts to obtain samples that truly represent the total ballast water onboard a vessel. A known cell density...

  3. High - velocity water jet impact on concrete samples

    Czech Academy of Sciences Publication Activity Database

    Mádr, V.; Uhlář, R.; Hlaváč, L. M.; Sitek, Libor; Foldyna, Josef; Hela, R.; Bodnárová, L.; Kaličinský, J.

    2009-01-01

    Roč. 2, č. 4 (2009), s. 43-48 ISSN 2067-3809 Institutional research plan: CEZ:AV0Z30860518 Keywords : water jet * concrete * depth of penetration * disintegration volume Subject RIV: JM - Building Engineering http://acta.fih.upt.ro/pdf/2009-4/ACTA-2009-4-08.pdf

  4. Beryllium-10 concentrations in water samples of high northern latitudes

    Energy Technology Data Exchange (ETDEWEB)

    Strobl, C.; Eisenhauer, A.; Schulz, V.; Baumann, S.; Mangini, A. [Heidelberger Akademie der Wissenschaften, Heildelberg (Germany); Kubik, P.W. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1997-09-01

    {sup 10}Be concentrations in the water column of high northern latitudes were not available so far. We present different {sup 10}Be profiles from the Norwegian-Greenland Sea, the Arctic Ocean, and the Laptev Sea. (author) 3 fig., 3 refs.

  5. Identifying potential surface water sampling sites for emerging ...

    African Journals Online (AJOL)

    Emerging chemical pollutants (ECPs) are defined as new chemicals which do not have a regulatory status, but which may have an adverse effect on human health and the environment. The occurrence and concentrations of ECPs in South African water bodies are largely unknown, so monitoring is required in order to ...

  6. Sample container and storage for paclobutrazol monitoring in irrigation water

    Science.gov (United States)

    Paclobutrazol is a plant growth retardant commonly used on greenhouse crops. Residues from paclobutrazol applications can accumulate in recirculated irrigation water. Given that paclobutrazol has a long half-life and potential biological activity in parts per billion concentrations, it would be de...

  7. UMTRA Project water sampling and analysis plan, Grand Junction, Colorado. Revision 1, Version 6

    International Nuclear Information System (INIS)

    1995-09-01

    This water sampling and analysis plan describes the planned, routine ground water sampling activities at the Grand Junction US DOE Uranium Mill Tailings Remedial Action (UMTRA) Project site (GRJ-01) in Grand Junction, Colorado, and at the Cheney Disposal Site (GRJ-03) near Grand Junction. The plan identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequencies for the routine monitoring stations at the sites. Regulatory basis is in the US EPA regulations in 40 CFR Part 192 (1994) and EPA ground water quality standards of 1995 (60 FR 2854). This plan summarizes results of past water sampling activities, details water sampling activities planned for the next 2 years, and projects sampling activities for the next 5 years

  8. Polymeric ionic liquid-based portable tip microextraction device for on-site sample preparation of water samples.

    Science.gov (United States)

    Chen, Lei; Pei, Junxian; Huang, Xiaojia; Lu, Min

    2018-06-05

    On-site sample preparation is highly desired because it avoids the transportation of large-volume samples and ensures the accuracy of the analytical results. In this work, a portable prototype of tip microextraction device (TMD) was designed and developed for on-site sample pretreatment. The assembly procedure of TMD is quite simple. Firstly, polymeric ionic liquid (PIL)-based adsorbent was in-situ prepared in a pipette tip. After that, the tip was connected with a syringe which was driven by a bidirectional motor. The flow rates in adsorption and desorption steps were controlled accurately by the motor. To evaluate the practicability of the developed device, the TMD was used to on-site sample preparation of waters and combined with high-performance liquid chromatography with diode array detection to measure trace estrogens in water samples. Under the most favorable conditions, the limits of detection (LODs, S/N = 3) for the target analytes were in the range of 4.9-22 ng/L, with good coefficients of determination. Confirmatory study well evidences that the extraction performance of TMD is comparable to that of the traditional laboratory solid-phase extraction process, but the proposed TMD is more simple and convenient. At the same time, the TMD avoids complicated sampling and transferring steps of large-volume water samples. Copyright © 2018 Elsevier B.V. All rights reserved.

  9. SEAMIST trademark soil sampling for tritiated water: First year's results

    International Nuclear Information System (INIS)

    Mallon, B.; Martins, S.A.; Houpis, J.L.; Lowry, W.; Cremer, C.D.

    1992-01-01

    SEAMIST trademark is a recently developed sampling system that enables one to measure various soil parameters by means of an inverted, removable, impermeable membrane tube inserted in a borehole. This membrane tube can have various measuring devices installed on it, such as gas ports, adsorbent pads, and electrical sensors. These membrane tubes are made of a laminated polymer. The Lawrence Livermore National Laboratory in Livermore, California, has installed two of these systems to monitor tritium in soil resulting from a leak in an underground storage tank. One tube is equipped with gas ports to sample soil vapor and the other with adsorbent pads to sample soil moisture. Borehole stability was maintained using either sand-filled or air-inflated tubes. Both system implementations yielded concentrations or activities that compared well with the measured concentrations of tritium in the soil taken during borehole construction. In addition, an analysis of the data suggest that both systems prevented the vertical migration of tritium in the boreholes. Also, a neutron probe was successfully used in a blank membrane inserted in one of the boreholes to monitor the moisture in the soil without exposing the probe to the tritium. The neutron log showed excellent agreement with the soil moisture content measured in soil samples taken during borehole construction. This paper describes the two SEAMIST trademark systems used and presents sampling results and comparisons

  10. UMTRA Project water sampling and analysis plan, Gunnison, Colorado: Revision 1

    International Nuclear Information System (INIS)

    1994-11-01

    This water sampling and analysis plan summarizes the results of previous water sampling activities and the plan for future water sampling activities, in accordance with the Guidance Document for Preparing Sampling and Analysis Plans for UMTRA Sites. A buffer zone monitoring plan for the Dos Rios Subdivision is included as an appendix. The buffer zone monitoring plan was developed to ensure continued protection to the public from residual contamination. The buffer zone is beyond the area depicted as contaminated ground water due to former milling operations. Surface remedial action at the Gunnison Uranium Mill Tailings Remedial Action Project site began in 1992; completion is expected in 1995. Ground water and surface water will be sampled semiannually at the Gunnison processing site and disposal site. Results of previous water sampling at the Gunnison processing site indicate that ground water in the alluvium is contaminated by the former uranium processing activities. Background ground water conditions have been established in the uppermost aquifer at the Gunnison disposal site. The monitor well locations provide a representative distribution of sampling points to characterize ground water quality and ground water flow conditions in the vicinity of the sites. The list of analytes has been modified with time to reflect constituents that are related to uranium processing activities and the parameters needed for geochemical evaluation

  11. Total and inorganic arsenic in fish samples from Norwegian waters.

    Science.gov (United States)

    Julshamn, Kaare; Nilsen, Bente M; Frantzen, Sylvia; Valdersnes, Stig; Maage, Amund; Nedreaas, Kjell; Sloth, Jens J

    2012-01-01

    The contents of total arsenic and inorganic arsenic were determined in fillet samples of Northeast Artic cod, herring, mackerel, Greenland halibut, tusk, saithe and Atlantic halibut. In total, 923 individual fish samples were analysed. The fish were mostly caught in the open sea off the coast of Norway, from 40 positions. The determination of total arsenic was carried out by inductively coupled plasma mass spectrometry following microwave-assisted wet digestion. The determination of inorganic arsenic was carried out by high-performance liquid chromatography-ICP-MS following microwave-assisted dissolution of the samples. The concentrations found for total arsenic varied greatly between fish species, and ranged from 0.3 to 110 mg kg(-1) wet weight. For inorganic arsenic, the concentrations found were very low (fish used in the recent EFSA opinion on arsenic in food.

  12. Determination of Phenols in Water Samples using a Supported ...

    African Journals Online (AJOL)

    NJD

    This was achieved by pH adjustments in the sample and acceptor phases. The method was ... during wastewater treatment, since chlorine is added as a disinfectant. ... they give a high degree of selectivity and clean-up, use little or no organic ...

  13. UMTRA Project water sampling and analysis plan, Belfield and Bowman, North Dakota

    International Nuclear Information System (INIS)

    1994-08-01

    Surface remedial action is scheduled to begin at the Belfield and Bowman Uranium Mill Tailings Remedial Action (UMTRA) Project sites in the spring of 1996. Water sampling was conducted in 1993 at both the Belfield processing site and the Bowman processing/disposal site. Results of the sampling at both sites indicate that ground water conditions have remained relatively stable over time. Water sampling activities are not scheduled for 1994 because ground water conditions at the two sites are relatively stable, the 1993 sampling was comprehensive, and surface remediation activities are not scheduled to start until 1996. The next water sampling event is scheduled before the start of remedial activities and will include sampling selected monitor wells at both sites and several domestic wells in the vicinity

  14. Concentration of polycyclic aromatic hydrocarbons in water samples from different stages of treatment

    Science.gov (United States)

    Pogorzelec, Marta; Piekarska, Katarzyna

    2017-11-01

    The aim of this study was to analyze the presence and concentration of selected polycyclic aromatic hydrocarbons in water samples from different stages of treatment and to verify the usefulness of semipermeable membrane devices for analysis of drinking water. For this purpose, study was conducted for a period of 5 months. Semipermeable membrane devices were deployed in a surface water treatment plant located in Lower Silesia (Poland). To determine the effect of water treatment on concentration of PAHs, three sampling places were chosen: raw water input, stream of water just before disinfection and treated water output. After each month of sampling SPMDs were changed for fresh ones and prepared for further analysis. Concentrations of fifteen polycyclic aromatic hydrocarbons were determined by high performance liquid chromatography (HPLC). Presented study indicates that the use of semipermeable membrane devices can be an effective tool for the analysis of aquatic environment, including monitoring of drinking water, where organic micropollutants are present at very low concentrations.

  15. Procedures for field chemical analyses of water samples

    International Nuclear Information System (INIS)

    Korte, N.; Ealey, D.

    1983-12-01

    A successful water-quality monitoring program requires a clear understanding of appropriate measurement procedures in order to obtain reliable field data. It is imperative that the responsible personnel have a thorough knowledge of the limitations of the techniques being used. Unfortunately, there is a belief that field analyses are simple and straightforward. Yet, significant controversy as well as misuse of common measurement techniques abounds. This document describes procedures for field measurements of pH, carbonate and bicarbonate, specific conductance, dissolved oxygen, nitrate, Eh, and uranium. Each procedure section includes an extensive discussion regarding the limitations of the method as well as brief discussions of calibration procedures and available equipment. A key feature of these procedures is the consideration given to the ultimate use of the data. For example, if the data are to be used for geochemical modeling, more precautions are needed. In contrast, routine monitoring conducted merely to recognize gross changes can be accomplished with less effort. Finally, quality assurance documentation for each measurement is addressed in detail. Particular attention is given to recording sufficient information such that decisions concerning the quality of the data can be easily made. Application of the procedures and recommendations presented in this document should result in a uniform and credible water-quality monitoring program. 22 references, 4 figures, 3 tables

  16. Determination of rare earth elements in natural water samples – A review of sample separation, preconcentration and direct methodologies

    Energy Technology Data Exchange (ETDEWEB)

    Fisher, Andrew, E-mail: afisher@plymouth.ac.uk [School of Geography, Earth and Environmental Sciences, Plymouth University, Drake Circus, Plymouth, Devon, PL4 8AA (United Kingdom); Kara, Derya [Department of Chemistry, Art and Science Faculty, Balikesir University, 10100, Balikesir (Turkey)

    2016-09-07

    This review discusses and compares the methods given for the determination of rare earth elements (REE) in natural water samples, including sea, river, lake, tap, ground and waste waters as well as Antarctic ice. Since REE are at very low concentrations in natural waters, numerous different preconcentration methods have been proposed to enable their measurement. These include liquid liquid extraction, dispersive liquid-liquid micro-extraction and solidified floating drop micro-extraction. In addition to liquid-liquid extraction methods, solid phase extraction using commercial resins, resins made in-house, silica-based exchange materials and other solid media is also discussed. These and other techniques such as precipitation/co-precipitation and flotation are compared in terms of speed, preconcentration factors achieved, precision, accuracy and limits of detection (LOD). Some papers have discussed the direct determination of REE in these sample types. Some have used specialised sample introduction systems such as ultrasonic nebulization whereas others have used a standard sample introduction system coupled with inductively coupled plasma mass spectrometry (ICP-MS) detection. These direct methods have also been discussed and compared. - Highlights: • The determination of rare earth elements in waters is reviewed. • Assorted preconcentration techniques are discussed and evaluated. • Detection techniques include atomic spectrometry, potentiometry and spectrophotometry. • Special nebulisers and electrothermal vaporization approaches are reviewed.

  17. 222Rn in water: A comparison of two sample collection methods and two sample transport methods, and the determination of temporal variation in North Carolina ground water

    International Nuclear Information System (INIS)

    Hightower, J.H. III

    1994-01-01

    Objectives of this field experiment were: (1) determine whether there was a statistically significant difference between the radon concentrations of samples collected by EPA's standard method, using a syringe, and an alternative, slow-flow method; (2) determine whether there was a statistically significant difference between the measured radon concentrations of samples mailed vs samples not mailed; and (3) determine whether there was a temporal variation of water radon concentration over a 7-month period. The field experiment was conducted at 9 sites, 5 private wells, and 4 public wells, at various locations in North Carolina. Results showed that a syringe is not necessary for sample collection, there was generally no significant radon loss due to mailing samples, and there was statistically significant evidence of temporal variations in water radon concentrations

  18. [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.

  19. UMTRA Project water sampling and analysis plan, Gunnison, Colorado. Revision 2

    International Nuclear Information System (INIS)

    1995-09-01

    Surface remedial action at the Gunnison Uranium Mill Tailings Remedial Action Project site began in 1992; completion is expected in 1995. Ground water and surface water will be sampled semiannually at the Gunnison processing site (GUN-01) and disposal site (GUN-08). Results of previous water sampling at the Gunnison processing site indicate that ground water in the alluvium is contaminated by the former uranium processing activities. Background ground water conditions have been established in the uppermost aquifer (Tertiary gravels) at the Gunnison disposal site. Semiannual water sampling is scheduled for the spring and fall. Water quality sampling is conducted at the processing site (1) to ensure protection of human health and the environment, (2) for ground water compliance monitoring during remedial action construction, and (3) to define the extent of contamination. At the processing site, the frequency and duration of sampling will be dependent upon the nature and extent of residual contamination and the compliance strategy chosen. The monitor well locations provide a representative distribution of sampling points to characterize ground water quality and ground water flow conditions in the vicinity of the sites. The list of analytes has been modified with time to reflect constituents that are related to uranium processing activities and the parameters needed for geochemical evaluation

  20. Determination of radiocesium in environmental water samples using copper ferro(II)cyanide and sodium tetraphenylborate

    International Nuclear Information System (INIS)

    Popov, L.; Kuleff, I.; Djingova, R.

    2006-01-01

    A procedure for the radiochemical separation and radiochemical purification of radiocesium ( 134 Cs and 137 Cs) in bulk environmental water samples is proposed. Radiocesium was removed from the water by cation-exchange with copper ferro(II)cyanide and was purified by precipitation with sodium tetraphenylborate. The influence of the concentration of potassium in the water sample on the chemical yield was investigated. The validation of the proposed method was carried out by analyzing reference materials. The application of the method was demonstrated with the determination of the concentration of radiocesium in water samples from rivers around NPP 'Kozloduy', Bulgaria, Danube and Ogosta. (author)

  1. Uranium content measurement in drinking water samples using track etch technique

    International Nuclear Information System (INIS)

    Kumar, Mukesh; Kumar, Ajay; Singh, Surinder; Mahajan, R.K.; Walia, T.P.S.

    2003-01-01

    The concentration of uranium has been assessed in drinking water samples collected from different locations in Bathinda district, Punjab, India. The water samples are taken from hand pumps and tube wells. Uranium is determined using fission track technique. Uranium concentration in the water samples varies from 1.65±0.06 to 74.98±0.38 μg/l. These values are compared with safe limit values recommended for drinking water. Most of the water samples are found to have uranium concentration above the safe limit. Analysis of some heavy metals (Zn, Cd, Pb and Cu) in water is also done in order to see if some correlation exists between the concentration of uranium and these heavy metals. A weak positive correlation has been observed between the concentration of uranium and heavy metals of Pb, Cd and Cu

  2. USDA Forest Service national protocols for sampling air pollution-sensitive waters

    Science.gov (United States)

    T. J. Sullivan

    2012-01-01

    The first step in designing a surface water sampling program is identifying one or more problems or questions that require information on water quality. Common water quality problems include nutrient enrichment (from a variety of causes), effects of atmospheric deposition (acidification, eutrophication, toxicity), and effects of major disturbances such as fire or pest...

  3. Evaluation of the Bacterial Status of Water Samples at Umudike Abia ...

    African Journals Online (AJOL)

    77.78%), Proteus spp.(66.67%), Serratia spp.(55.5%) and Vibro spp.(22.2%). The occurrence of the water borne pathogens appeared limited to the stream water samples, hence, continuous consumption without adequate treatment is potentially dangerous. Keywords: Water, rainwater, stream, bacteria, coliforms, pathogen ...

  4. UMTRA Project water sampling and analysis plan, Durango, Colorado. Revision 1

    International Nuclear Information System (INIS)

    1995-09-01

    Planned, routine ground water sampling activities at the US Department of Energy (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project site in Durango, Colorado, are described in this water sampling and analysis plan. The plan identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequency for the routine monitoring stations at the site. The ground water data are used to characterize the site ground water compliance strategies and to monitor contaminants of potential concern identified in the baseline risk assessment (DOE, 1995a). Regulatory basis for routine ground water monitoring at UMTRA Project sites is derived from the US EPA regulations in 40 CFR Part 192 (1994) and EPA standards of 1995 (60 FR 2854). Sampling procedures are guided by the UMTRA Project standard operating procedures (SOP) (JEG, n.d.), the Technical Approach Document (TAD) (DOE, 1989), and the most effective technical approach for the site

  5. Water sampling using a drone at Yugama crater lake, Kusatsu-Shirane volcano, Japan

    Science.gov (United States)

    Terada, Akihiko; Morita, Yuichi; Hashimoto, Takeshi; Mori, Toshiya; Ohba, Takeshi; Yaguchi, Muga; Kanda, Wataru

    2018-04-01

    Remote sampling of water from Yugama crater lake at Kusatsu-Shirane volcano, Japan, was performed using a drone. Despite the high altitude of over 2000 m above sea level, our simple method was successful in retrieving a 250 mL sample of lake water. The procedure presented here is easy for any researcher to follow who operates a drone without additional special apparatus. We compare the lake water sampled by drone with that sampled by hand at a site where regular samplings have previously been carried out. Chemical concentrations and stable isotope ratios are largely consistent between the two techniques. As the drone can fly automatically with the aid of navigation by Global Navigation Satellite System (GNSS), it is possible to repeatedly sample lake water from the same location, even when entry to Yugama crater lake is restricted due to the risk of eruption.[Figure not available: see fulltext.

  6. National Coral Reef Monitoring Program: Water Chemistry of the Coral Reefs in American Samoa from Water Samples collected since 2015

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water samples are collected and analyzed to assess spatial and temporal variation in the seawater carbonate systems of coral reef ecosystems in the Hawaiian and...

  7. UMTRA project water sampling and analysis plan, Salt Lake City, Utah

    International Nuclear Information System (INIS)

    1994-06-01

    Surface remedial action was completed at the Salt Lake City, Utah, Uranium Mill Tailings Remedial Action (UMTRA) Project site in the fall of 1987. Results of water sampling for the years 1992 to 1994 indicate that site-related ground water contamination occurs in the shallow unconfined aquifer (the uppermost aquifer). With respect to background ground water quality, contaminated ground water in the shallow, unconfined aquifer has elevated levels of chloride, sodium, sulfate, total dissolved solids, and uranium. No contamination associated with the former tailings pile occurs in levels exceeding background in ground water in the deeper confined aquifer. This document provides the water sampling and analysis plan for ground water monitoring at the former uranium processing site in Salt Lake City, Utah (otherwise known as the ''Vitro'' site, named after the Vitro Chemical Company that operated the mill). All contaminated materials removed from the processing site were relocated and stabilized in a disposal cell near Clive, Utah, some 85 miles west of the Vitro site (known as the ''Clive'' disposal site). No ground water monitoring is being performed at the Clive disposal site, since concurrence of the remedial action plan by the US Nuclear Regulatory Commission and completion of the disposal cell occurred before the US Environmental Protection Agency issued draft ground water standards in 1987 (52 FR 36000) for cleanup, stabilization, and control of residual radioactive materials at the disposal site. In addition, the likelihood of post-closure impact on the ground water is minimal to nonexistent, due to the naturally poor quality of the ground water. Water sampling activities planned for calendar year 1994 consist of sampling ground water from nine monitor wells to assess the migration of contamination within the shallow unconfined aquifer and sampling ground water from two existing monitor wells to assess ground water quality in the confined aquifer

  8. Enrichment and determination of small amounts of 90Sr/90Y in water samples

    International Nuclear Information System (INIS)

    Mundschenk, H.

    1979-01-01

    Small amounts of 90 Sr/ 90 Y can be concentrated from large volumes of surface water (100 l) by precipitation of the phosphates, using bentonite as adsorber matrix. In the case of samples containing no or nearly no suspended matter (tap water, ground water, sea water), the daughter 90 Y can be extracted directly by using filter beds impregnated with HDEHP. The applicability of both techniques is demonstrated under realistic conditions. (orig.) 891 HP/orig. 892 MKO [de

  9. Determination of pyridine in soil and water samples of a polluted area

    International Nuclear Information System (INIS)

    Peters, R.J.B.; Renesse van Duivenbode, J.A.D. van

    1994-01-01

    A method for the analyses of pyridine in environmental samples is described. For soil samples a distillation procedure followed by an extraction, an acidic extraction or a Soxhlet extraction can be used. For water samples a distillation procedure followed by extraction can be employed. Deuterated pyridine is used as an internal standard and the extracts are analyzed by GC-MS. The recoveries of the methods are higher than 80%; the detection limits for pyridine are 0.01 mg/kg for soil samples and 0.2 μg/l for water samples. (orig.)

  10. Water quality monitoring: A comparative case study of municipal and Curtin Sarawak's lake samples

    Science.gov (United States)

    Anand Kumar, A.; Jaison, J.; Prabakaran, K.; Nagarajan, R.; Chan, Y. S.

    2016-03-01

    In this study, particle size distribution and zeta potential of the suspended particles in municipal water and lake surface water of Curtin Sarawak's lake were compared and the samples were analysed using dynamic light scattering method. High concentration of suspended particles affects the water quality as well as suppresses the aquatic photosynthetic systems. A new approach has been carried out in the current work to determine the particle size distribution and zeta potential of the suspended particles present in the water samples. The results for the lake samples showed that the particle size ranges from 180nm to 1345nm and the zeta potential values ranges from -8.58 mV to -26.1 mV. High zeta potential value was observed in the surface water samples of Curtin Sarawak's lake compared to the municipal water. The zeta potential values represent that the suspended particles are stable and chances of agglomeration is lower in lake water samples. Moreover, the effects of physico-chemical parameters on zeta potential of the water samples were also discussed.

  11. Recovery of diverse microbes in high turbidity surface water samples using dead-end ultrafiltration.

    Science.gov (United States)

    Mull, Bonnie; Hill, Vincent R

    2012-12-01

    Dead-end ultrafiltration (DEUF) has been reported to be a simple, field-deployable technique for recovering bacteria, viruses, and parasites from large-volume water samples for water quality testing and waterborne disease investigations. While DEUF has been reported for application to water samples having relatively low turbidity, little information is available regarding recovery efficiencies for this technique when applied to sampling turbid water samples such as those commonly found in lakes and rivers. This study evaluated the effectiveness of a DEUF technique for recovering MS2 bacteriophage, enterococci, Escherichia coli, Clostridium perfringens, and Cryptosporidium parvum oocysts in surface water samples having elevated turbidity. Average recovery efficiencies for each study microbe across all turbidity ranges were: MS2 (66%), C. parvum (49%), enterococci (85%), E. coli (81%), and C. perfringens (63%). The recovery efficiencies for MS2 and C. perfringens exhibited an inversely proportional relationship with turbidity, however no significant differences in recovery were observed for C. parvum, enterococci, or E. coli. Although ultrafilter clogging was observed, the DEUF method was able to process 100-L surface water samples at each turbidity level within 60 min. This study supports the use of the DEUF method for recovering a wide array of microbes in large-volume surface water samples having medium to high turbidity. Published by Elsevier B.V.

  12. Pesticide residues analysis in water samples of Nagarpur and Saturia Upazila, Bangladesh

    Science.gov (United States)

    Hasanuzzaman, M.; Rahman, M. A.; Islam, M. S.; Salam, M. A.; Nabi, M. R.

    2018-03-01

    Pesticides used to protect the crops from pest attack in the agricultural fields pose harmful effect to the non-target organisms such as human and many other aquatic and terrestrial organisms either directly or indirectly through food chain. The present study was conducted to monitor a total of seven pesticide residues under organochlorine, organophosphorus and carbamate pesticides in three different sources of pond water, paddy field water and tube-well water from Nagarpur Upazila and paddy field water in the company of Dhaleshwari and Gazikhali river water from Saturia Upazila, Bangladesh. A total of 40 water samples were analyzed using high-performance liquid chromatography equipped with ultraviolet detector. Among the organophosphorus pesticides, diazinon was detected in eight water samples at a concentration ranging from 4.11 to 257.91 μg/l whereas, malathion was detected only in one water sample at a concentration of 84.64 μg/l and chlorpyrifos pesticide was also detected only in one water sample and the concentration was 37.3 μg/l. Trace amount of carbaryl was identified but it was below the detection limit. None of the tested water samples was found to be contaminated with DDT or its metabolites (DDE and DDD). The water samples contaminated with the suspected pesticides were above the acceptable limit except for the fish pond samples of Sahabatpur and Dubaria union. To control the misuse of pesticides and to reduce the possible health risk, appropriate control systems of pests such as integrated pest management system should be implemented immediately by the authorities of the country.

  13. First Total Reflection X-Ray Fluorescence round-robin test of water samples: Preliminary results

    Energy Technology Data Exchange (ETDEWEB)

    Borgese, Laura; Bilo, Fabjola [Chemistry for Technologies Laboratory, University of Brescia, Brescia (Italy); Tsuji, Kouichi [Graduate School of Engineering, Osaka City University, Osaka (Japan); Fernández-Ruiz, Ramón [Servicio Interdepartamental de Investigación (SIdI), Laboratorio de TXRF, Universidad Autónoma de Madrid, Madrid (Spain); Margui, Eva [Department of Chemistry, University of Girona, Girona (Spain); Streli, Christina [TU Wien, Atominstitut,Radiation Physics, Vienna (Austria); Pepponi, Giancarlo [Fondazione Bruno Kessler, Povo, Trento (Italy); Stosnach, Hagen [Bruker Nano GmbH, Berlin (Germany); Yamada, Takashi [Rigaku Corporation, Takatsuki, Osaka (Japan); Vandenabeele, Peter [Department of Archaeology, Ghent University, Ghent (Belgium); Maina, David M.; Gatari, Michael [Institute of Nuclear Science and Technology, University of Nairobi, Nairobi (Kenya); Shepherd, Keith D.; Towett, Erick K. [World Agroforestry Centre (ICRAF), Nairobi (Kenya); Bennun, Leonardo [Laboratorio de Física Aplicada, Departamento de Física, Universidad de Concepción (Chile); Custo, Graciela; Vasquez, Cristina [Gerencia Química, Laboratorio B025, Centro Atómico Constituyentes, San Martín (Argentina); Depero, Laura E., E-mail: laura.depero@unibs.it [Chemistry for Technologies Laboratory, University of Brescia, Brescia (Italy)

    2014-11-01

    Total Reflection X-Ray Fluorescence (TXRF) is a mature technique to evaluate quantitatively the elemental composition of liquid samples deposited on clean and well polished reflectors. In this paper the results of the first worldwide TXRF round-robin test of water samples, involving 18 laboratories in 10 countries are presented and discussed. The test was performed within the framework of the VAMAS project, interlaboratory comparison of TXRF spectroscopy for environmental analysis, whose aim is to develop guidelines and a standard methodology for biological and environmental analysis by means of the TXRF analytical technique. - Highlights: • The discussion of the first worldwide TXRF round-robin test of water samples (18 laboratories of 10 countries) is reported. • Drinking, waste, and desalinated water samples were tested. • Data dispersion sources were identified: sample concentration, preparation, fitting procedure, and quantification. • The protocol for TXRF analysis of drinking water is proposed.

  14. Presence of pesticide residues in water, sediment and biological samples taken from aquatic environments in Honduras

    International Nuclear Information System (INIS)

    Meyer, D.E.

    1999-01-01

    The objective of this study was to detect the presence of persistent pesticides in water, sediment and biological samples taken from aquatic environments in Honduras during the period 1995-98. Additionally, the LC 50 for 2 fungicides and 2 insecticides on post-larval Penaeus vannamei was determined in static water bioassays. A total of 80 water samples, 16 sediment samples and 7 biological samples (fish muscle tissue) were analyzed for detection of organochlorine and organophosphate pesticide residues. The results of sample analyses indicate a widespread contamination of Honduran continental and coastal waters with organochlorine pesticides. Most detections were of low ( 50 values and were therefore found to be much more toxic to the post-larval shrimp than the fungicides tridemorph and propiconazole. (author)

  15. A QUANTITATIVE EVALUATION OF THE WATER DISTRIBUTION IN A SOIL SAMPLE USING NEUTRON IMAGING

    Directory of Open Access Journals (Sweden)

    Jan Šácha

    2016-10-01

    Full Text Available This paper presents an empirical method by Kang et al. recently proposed for correcting two-dimensional neutron radiography for water quantification in soil. The method was tested on data from neutron imaging of the water infiltration in a soil sample. The raw data were affected by neutron scattering and by beam hardening artefacts. Two strategies for identifying the correction parameters are proposed in this paper. The method has been further developed for the case of three-dimensional neutron tomography. In a related experiment, neutron imaging is used to record ponded-infiltration experiments in two artificial soil samples. Radiograms, i.e., two-dimensional projections of the sample, were acquired during infiltration. A calculation was made of the amount of water and its distribution within the radiograms, in the form of two-dimensional water thickness maps. Tomograms were reconstructed from the corrected and uncorrected water thickness maps to obtain the 3D spatial distribution of the water content within the sample. Without the correction, the beam hardening and the scattering effects overestimated the water content values close to the perimeter of the sample, and at the same time underestimated the values close to the centre of the sample. The total water content of the entire sample was the same in both cases. The empirical correction method presented in this study is a relatively accurate, rapid and simple way to obtain the quantitatively determined water content from two-dimensional and three-dimensional neutron images. However, an independent method for measuring the total water volume in the sample is needed in order to identify the correction parameters.

  16. Sampling designs and methods for estimating fish-impingement losses at cooling-water intakes

    International Nuclear Information System (INIS)

    Murarka, I.P.; Bodeau, D.J.

    1977-01-01

    Several systems for estimating fish impingement at power plant cooling-water intakes are compared to determine the most statistically efficient sampling designs and methods. Compared to a simple random sampling scheme the stratified systematic random sampling scheme, the systematic random sampling scheme, and the stratified random sampling scheme yield higher efficiencies and better estimators for the parameters in two models of fish impingement as a time-series process. Mathematical results and illustrative examples of the applications of the sampling schemes to simulated and real data are given. Some sampling designs applicable to fish-impingement studies are presented in appendixes

  17. Estimation of uranium in drinking water samples collected from different locations across Tarapur, India

    International Nuclear Information System (INIS)

    Dusane, C.B.; Maity, Sukanta; Sahu, S.K.; Pandit, G.G.

    2015-01-01

    In this study, drinking water samples were collected from different locations across Tarapur, India for screening uranium contents. Uranium concentrations were determined by differential pulse adsorptive stripping voltammetry (DPASV). Uranium concentration in water samples varied in a wide range from 0.6-7.9 μg L -1 . Results were compared with the international water quality guidelines World Health Organization (WHO, 2011) and were found within the permissible limit. Results were also compared with the safe limit values for drinking water recommended by national organization like Atomic Energy Regulatory Board (AERB). (author)

  18. Evaluation of the Purge Water Management System (PWMS) monitor well sampling technology at SRS

    International Nuclear Information System (INIS)

    Hiergesell, R.A.; Cardoso-Neto, J.E.; Williams, D.W.

    1997-01-01

    Due to the complex issues surrounding Investigation Derived Waste (IDW) at SRS, the Environmental Restoration Division has been exploring new technologies to deal with the purge water generated during monitoring well sampling. Standard procedures for sampling generates copious amounts of purge water that must be managed as hazardous waste, when containing hazardous and/or radiological contaminants exceeding certain threshold levels. SRS has obtained Regulator approval to field test an innovative surface release prevention mechanism to manage purge water. This mechanism is referred to as the Purge Water Management System (PWMS) and consists of a collapsible bladder situated within a rigid metal tank

  19. Uranium and thorium determination in water samples taken along River Kura

    International Nuclear Information System (INIS)

    Ahmadov, M.M.; Ibadov, N.A.; Safarova, K.S.; Humbatov, F.Y.; Suleymanov, B.A.

    2014-01-01

    Full text : In the present investigation, uranium and thorium concentration in rivers water of Azerbaijan has been measured using inductively coupled plasma mass spectrometry. The Agilent 7700x series ICP-MS applied for analysis of water samples. This method is based on direct introduction of samples, without any chemical pre-treatment, into an inductively coupled plasma plasma mass spectrometer. Uranium and thorium was determined at the mass mass numbers of 238 and 232 respectively using Bi-209 as internal standard. The main purpose of the study is to measure the level of uranium and thorium in water samples taken along river Kura

  20. Estimating an appropriate sampling frequency for monitoring ground water well contamination

    International Nuclear Information System (INIS)

    Tuckfield, R.C.

    1994-01-01

    Nearly 1,500 ground water wells at the Savannah River Site (SRS) are sampled quarterly to monitor contamination by radionuclides and other hazardous constituents from nearby waste sites. Some 10,000 water samples were collected in 1993 at a laboratory analysis cost of $10,000,000. No widely accepted statistical method has been developed, to date, for estimating a technically defensible ground water sampling frequency consistent and compliant with federal regulations. Such a method is presented here based on the concept of statistical independence among successively measured contaminant concentrations in time

  1. Monitoring the aftermath of Flint drinking water contamination crisis: Another case of sampling bias?

    Science.gov (United States)

    Goovaerts, Pierre

    2017-07-15

    The delay in reporting high levels of lead in Flint drinking water, following the city's switch to the Flint River as its water supply, was partially caused by the biased selection of sampling sites away from the lead pipe network. Since Flint returned to its pre-crisis source of drinking water, the State has been monitoring water lead levels (WLL) at selected "sentinel" sites. In a first phase that lasted two months, 739 residences were sampled, most of them bi-weekly, to determine the general health of the distribution system and to track temporal changes in lead levels. During the same period, water samples were also collected through a voluntary program whereby concerned citizens received free testing kits and conducted sampling on their own. State officials relied on the former data to demonstrate the steady improvement in water quality. A recent analysis of data collected by voluntary sampling revealed, however, an opposite trend with lead levels increasing over time. This paper looks at potential sampling bias to explain such differences. Although houses with higher WLL were more likely to be sampled repeatedly, voluntary sampling turned out to reproduce fairly well the main characteristics (i.e. presence of lead service lines (LSL), construction year) of Flint housing stock. State-controlled sampling was less representative; e.g., sentinel sites with LSL were mostly built between 1935 and 1950 in lower poverty areas, which might hamper our ability to disentangle the effects of LSL and premise plumbing (lead fixtures and pipes present within old houses) on WLL. Also, there was no sentinel site with LSL in two of the most impoverished wards, including where the percentage of children with elevated blood lead levels tripled following the switch in water supply. Correcting for sampling bias narrowed the gap between sampling programs, yet overall temporal trends are still opposite. Copyright © 2017 Elsevier B.V. All rights reserved.

  2. Understanding the origin and evolution of water in the Moon through lunar sample studies.

    Science.gov (United States)

    Anand, Mahesh; Tartèse, Romain; Barnes, Jessica J

    2014-09-13

    A paradigm shift has recently occurred in our knowledge and understanding of water in the lunar interior. This has transpired principally through continued analysis of returned lunar samples using modern analytical instrumentation. While these recent studies have undoubtedly measured indigenous water in lunar samples they have also highlighted our current limitations and some future challenges that need to be overcome in order to fully understand the origin, distribution and evolution of water in the lunar interior. Another exciting recent development in the field of lunar science has been the unambiguous detection of water or water ice on the surface of the Moon through instruments flown on a number of orbiting spacecraft missions. Considered together, sample-based studies and those from orbit strongly suggest that the Moon is not an anhydrous planetary body, as previously believed. New observations and measurements support the possibility of a wet lunar interior and the presence of distinct reservoirs of water on the lunar surface. Furthermore, an approach combining measurements of water abundance in lunar samples and its hydrogen isotopic composition has proved to be of vital importance to fingerprint and elucidate processes and source(s) involved in giving rise to the lunar water inventory. A number of sources are likely to have contributed to the water inventory of the Moon ranging from primordial water to meteorite-derived water ice through to the water formed during the reaction of solar wind hydrogen with the lunar soil. Perhaps two of the most striking findings from these recent studies are the revelation that at least some portions of the lunar interior are as water-rich as some Mid-Ocean Ridge Basalt source regions on Earth and that the water in the Earth and the Moon probably share a common origin. © 2014 The Author(s) Published by the Royal Society. All rights reserved.

  3. Design, analysis, and interpretation of field quality-control data for water-sampling projects

    Science.gov (United States)

    Mueller, David K.; Schertz, Terry L.; Martin, Jeffrey D.; Sandstrom, Mark W.

    2015-01-01

    The process of obtaining and analyzing water samples from the environment includes a number of steps that can affect the reported result. The equipment used to collect and filter samples, the bottles used for specific subsamples, any added preservatives, sample storage in the field, and shipment to the laboratory have the potential to affect how accurately samples represent the environment from which they were collected. During the early 1990s, the U.S. Geological Survey implemented policies to include the routine collection of quality-control samples in order to evaluate these effects and to ensure that water-quality data were adequately representing environmental conditions. Since that time, the U.S. Geological Survey Office of Water Quality has provided training in how to design effective field quality-control sampling programs and how to evaluate the resultant quality-control data. This report documents that training material and provides a reference for methods used to analyze quality-control data.

  4. Ionizing radiation as optimization method for aluminum detection from drinking water samples

    International Nuclear Information System (INIS)

    Bazante-Yamguish, Renata; Geraldo, Aurea Beatriz C.; Moura, Eduardo; Manzoli, Jose Eduardo

    2013-01-01

    The presence of organic compounds in water samples is often responsible for metal complexation; depending on the analytic method, the organic fraction may dissemble the evaluation of the real values of metal concentration. Pre-treatment of the samples is advised when organic compounds are interfering agents, and thus sample mineralization may be accomplished by several chemical and/or physical methods. Here, the ionizing radiation was used as an advanced oxidation process (AOP), for sample pre-treatment before the analytic determination of total and dissolved aluminum by ICP-OES in drinking water samples from wells and spring source located at Billings dam region. Before irradiation, the spring source and wells' samples showed aluminum levels of 0.020 mg/l and 0.2 mg/l respectively; after irradiation, both samples showed a 8-fold increase of aluminum concentration. These results are discussed considering other physical and chemical parameters and peculiarities of sample sources. (author)

  5. Analytical study on the determination of boron in environmental water samples

    International Nuclear Information System (INIS)

    Lopez, F.J.; Gimenez, E.; Hernandez, F.

    1993-01-01

    An analytical study on the determination of boron in environmental water samples was carried out. The curcumin and carmine standard methods were compared with the most recent Azomethine-H method in order to evaluate their analytical characteristics and feasibility for the analysis of boron in water samples. Analyses of synthetic water, ground water, sea water and waste water samples were carried out and a statistical evaluation of the results was made. The Azomethine-H method was found to be the most sensitive (detection limit 0.02 mg l -1 ) and selective (no interference of commonly occurring ions in water was observed), showing also the best precision (relative standard deviation lower than 4%). Moreover, it gave good results for all types of samples analyzed. The accuracy of this method was tested by the addition of known amounts of standard solutions to different types of water samples. The slopes of standard additions and direct calibration graphs were similar and recoveries of added boron ranged from 99 to 107%. (orig.)

  6. Estimation of uranium in different types of water and sand samples by adsorptive stripping voltammetry

    International Nuclear Information System (INIS)

    Bhalke, Sunil; Raghunath, Radha; Mishra, Suchismita; Suseela, B.; Tripathi, R.M.; Pandit, G.G.; Shukla, V.K.; Puranik, V.D.

    2005-01-01

    A method is standardized for the estimation of uranium by adsorptive stripping voltammetry using chloranilic acid (CAA) as complexing agent. The optimum parameters to get best sensitivity and good reproducibility for uranium were 60s adsorption time, pH 1.8, chloranilic acid (2x10 -4 M) and 0.002M EDTA. The peak potential under this condition was found to be -0.03 V. With these optimum parameters a sensitivity of 1.19 nA/nM uranium was observed. Detection limit for this optimum parameter was found to be 0.55 nM. This can be further improved by increasing adsorption time. Using this method, uranium was estimated in different type of water samples such as seawater, synthetic seawater, stream water, tap water, well water, bore well water and process water. This method has also been used for estimation of uranium in sand, organic solvent used for extraction of uranium from phosphoric acid and its raffinate. Sample digestion procedures used for estimation of uranium in various matrices are discussed. It has been observed from the analysis that the uranium peak potentials changes with matrix of the sample, hence, standard addition method is the best method to get reliable and accurate results. Quality assurance of the standardized method is verified by analyzing certified reference water sample from USDOE, participating intercomparison exercises and also by estimating uranium content in water samples both by differential pulse adsorptive stripping voltammetric and laser fluorimetric techniques. (author)

  7. Identification and quantification of pesticide residues in water samples of Dhamrai Upazila, Bangladesh

    Science.gov (United States)

    Hasanuzzaman, M.; Rahman, M. A.; Salam, M. A.

    2017-10-01

    Being agricultural country, different types of pesticides are widely used in Bangladesh to prevent the crop losses due to pest attack which are ultimately drain to the water bodies. The present study was conducted to identify and quantify the organochlorine (DDT, DDE and DDD), organophosphorus (malathion, diazinon and chloropyrifos) and carbamate (carbaryl) residues in water samples of different sources from Dhamrai upazila of Bangladesh using high performance liquid chromatography (HPLC) equipped with ultra violate (UV) detector. Thirty water samples from fish pond, cultivated land and tube-well were collected in winter season to analyze the pesticide residues. Among the organophosphorus pesticides, malathion was present in seven water samples ranging from 42.58 to 922.8 μg/L, whereas diazinon was detected in water sample-8 (WS-8) and the concentration was 31.5 μg/L. None of the tested water samples was found to be contaminated with chlorpyrifos, carbaryl or DDT and its metabolites (DDE and DDD). Except for a tube-well water sample, concentrations of the detected residues are above the acceptable limit for human body as assigned by different organizations. To avoid the possible health hazards, the indiscriminate application of pesticides should be restricted and various substitute products like bio-pesticide should be introduced in a broad scale as soon as possible.

  8. “Nanofiltration” Enabled by Super-Absorbent Polymer Beads for Concentrating Microorganisms in Water Samples

    Science.gov (United States)

    Xie, Xing; Bahnemann, Janina; Wang, Siwen; Yang, Yang; Hoffmann, Michael R.

    2016-01-01

    Detection and quantification of pathogens in water is critical for the protection of human health and for drinking water safety and security. When the pathogen concentrations are low, large sample volumes (several liters) are needed to achieve reliable quantitative results. However, most microbial identification methods utilize relatively small sample volumes. As a consequence, a concentration step is often required to detect pathogens in natural waters. Herein, we introduce a novel water sample concentration method based on superabsorbent polymer (SAP) beads. When SAP beads swell with water, small molecules can be sorbed within the beads, but larger particles are excluded and, thus, concentrated in the residual non-sorbed water. To illustrate this approach, millimeter-sized poly(acrylamide-co-itaconic acid) (P(AM-co-IA)) beads are synthesized and successfully applied to concentrate water samples containing two model microorganisms: Escherichia coli and bacteriophage MS2. Experimental results indicate that the size of the water channel within water swollen P(AM-co-IA) hydrogel beads is on the order of several nanometers. The millimeter size coupled with a negative surface charge of the beads are shown to be critical in order to achieve high levels of concentration. This new concentration procedure is very fast, effective, scalable, and low-cost with no need for complex instrumentation. PMID:26876979

  9. Methods for collecting algal samples as part of the National Water-Quality Assessment Program

    Science.gov (United States)

    Porter, Stephen D.; Cuffney, Thomas F.; Gurtz, Martin E.; Meador, Michael R.

    1993-01-01

    Benthic algae (periphyton) and phytoplankton communities are characterized in the U.S. Geological Survey's National Water-Quality Assessment Program as part of an integrated physical, chemical, and biological assessment of the Nation's water quality. This multidisciplinary approach provides multiple lines of evidence for evaluating water-quality status and trends, and for refining an understanding of the factors that affect water-quality conditions locally, regionally, and nationally. Water quality can be characterized by evaluating the results of qualitative and quantitative measurements of the algal community. Qualitative periphyton samples are collected to develop of list of taxa present in the sampling reach. Quantitative periphyton samples are collected to measure algal community structure within selected habitats. These samples of benthic algal communities are collected from natural substrates, using the sampling methods that are most appropriate for the habitat conditions. Phytoplankton samples may be collected in large nonwadeable streams and rivers to meet specific program objectives. Estimates of algal biomass (chlorophyll content and ash-free dry mass) also are optional measures that may be useful for interpreting water-quality conditions. A nationally consistent approach provides guidance on site, reach, and habitat selection, as well as information on methods and equipment for qualitative and quantitative sampling. Appropriate quality-assurance and quality-control guidelines are used to maximize the ability to analyze data locally, regionally, and nationally.

  10. Use of an Electronic Tongue System and Fuzzy Logic to Analyze Water Samples

    Science.gov (United States)

    Braga, Guilherme S.; Paterno, Leonardo G.; Fonseca, Fernando J.

    2009-05-01

    An electronic tongue (ET) system incorporating 8 chemical sensors was used in combination with two pattern recognition tools, namely principal component analysis (PCA) and Fuzzy logic for discriminating/classification of water samples from different sources (tap, distilled and three brands of mineral water). The Fuzzy program exhibited a higher accuracy than the PCA and allowed the ET to classify correctly 4 in 5 types of water. Exception was made for one brand of mineral water which was sometimes misclassified as tap water. On the other hand, the PCA grouped water samples in three clusters, one with the distilled water; a second with tap water and one brand of mineral water, and the third with the other two other brands of mineral water. Samples in the second and third clusters could not be distinguished. Nevertheless, close grouping between repeated tests indicated that the ET system response is reproducible. The potential use of the Fuzzy logic as the data processing tool in combination with an electronic tongue system is discussed.

  11. Genotoxicity assessment of water sampled from R-11 reservoir by means of allium test

    Energy Technology Data Exchange (ETDEWEB)

    Bukatich, E.; Pryakhin, E. [Urals Research Center for Radiation Medicine (Russian Federation); Geraskin, S. [Russian Institute of Agricultural Radiology and Agroecology (Russian Federation)

    2014-07-01

    The Mayak PA was the first enterprise for the production of weapon-grade plutonium in Russia and it incorporates uranium-graphite reactors for plutonium production and radiochemical facilities for its separation. Radiochemical processing resulted in huge volumes of liquid radioactive wastes of different specific activities. To reduce the radionuclides release into the environment, a system of bypasses and ponds (the Techa Cascade Reservoirs system) to store low-activity liquid wastes has been constructed in the upper reaches of the Techa River. Currently, industrial reservoirs of Mayak PA contain over 350 million m{sup 3} of low-level radioactive liquid wastes with total activity over 7.4 x 10{sup 15} Bq. Reservoir R-11 is the final reservoir in the Techa Cascade Reservoirs system. The average specific activity of main radionuclides in the water of R-11 are: {sup 90}Sr - 1.4x10{sup 3} Bq/l; {sup 137}Cs - 3 Bq/l; {sup 3}H - 7x10{sup 2} Bq/l; α-emitting radionuclides - 2.6 x 10{sup -1} Bq/l. In our study the Allium-test was employed to estimate reservoir R-11 water genotoxic effects. In 2012, 3 water samples were collected in different parts of reservoir R-11. Water samples from the Shershnevskoye reservoir (artificial reservoir on the Miass River designed for Chelyabinsk city water supply) were used as natural control. Samples of distilled and bottled water were used as an additional laboratory control. The common onion, Allium cepa L. (Stuttgarter Riesen) was used. Healthy equal-sized bulbs were soaked for 24 hours at +4±2 deg. C to synchronize cell division. The bulbs were maintained in distilled water at +23 deg. C until roots have grown up to 2±1 mm length and then plunged into water samples. Control samples remained in distilled and bottled water as well as in water samples from the Shershnevskoye reservoir (natural control). Roots of the 18±3 mm length were randomly sampled and fixed in an alcohol/acetic acid mixture. For microscopic analysis, squashed

  12. Prevalence of Cryptosporidium and Giardia lamblia in Water Samples from Jeddah and Makkah Cities

    Directory of Open Access Journals (Sweden)

    Haytham Ahmed Zakai

    2014-01-01

    Full Text Available Water contamination by Giardia lamblia and Cryptosporidium is one of the causes of diarrhoea throughout the world.  A total of 161 and 84 samples were collected from Jeddah and Makkah cities, respectively.  Each sample was concentrated by double centrifugation and the sediment was examined as a wet smear and after staining with Trichrome and Kinyoun stains.  The results showed that 56 (35% and 1 (0.62 % samples of Jeddah were positive for the oocyst of Cryptosporidium and cyst of Giardia, whereas only 21 (25% and 2 (2.4 % samples of Makkah showed positivity for oocysts and cyst of these parasites. Overall Cryptosporidium contamination in bottled water and water from filling stations was 6.8% and 17.4%, respectively. Maximum contamination for Cryptosporidium was recorded in tap water which was 51% and 25% in Jeddah and Makkah, respectively.

  13. Exploring the Legionella pneumophila positivity rate in hotel water samples from Antalya, Turkey.

    Science.gov (United States)

    Sepin Özen, Nevgün; Tuğlu Ataman, Şenay; Emek, Mestan

    2017-05-01

    The genus Legionella is a fastidious Gram-negative bacteria widely distributed in natural waters and man made water supply systems. Legionella pneumophila is the aetiological agent of approximately 90% of reported Legionellosis cases, and serogroup 1 is the most frequent cause of infections. Legionnaires' disease is often associated with travel and continues to be a public health concern at present. The correct water management quality practices and rapid methods for analyzing Legionella species in environmental water is a key point for the prevention of Legionnaires' disease outbreaks. This study aimed to evaluate the positivity rates and serotyping of Legionella species from water samples in the region of Antalya, Turkey, which is an important tourism center. During January-December 2010, a total of 1403 samples of water that were collected from various hotels (n = 56) located in Antalya were investigated for Legionella pneumophila. All samples were screened for L. pneumophila by culture method according to "ISO 11731-2" criteria. The culture positive Legionella strains were serologically identified by latex agglutination test. A total of 142 Legionella pneumophila isolates were recovered from 21 (37.5%) of 56 hotels. The total frequency of L. pneumophila isolation from water samples was found as 10.1%. Serological typing of 142 Legionella isolates by latex agglutination test revealed that strains belonging to L. pneumophila serogroups 2-14 predominated in the examined samples (85%), while strains of L. pneumophila serogroup 1 were less numerous (15%). According to our knowledge, our study with the greatest number of water samples from Turkey demonstrates that L. pneumophila serogroups 2-14 is the most common isolate. Rapid isolation of L. pneumophila from environmental water samples is essential for the investigation of travel related outbreaks and the possible resources. Further studies are needed to have epidemiological data and to determine the types of L

  14. Supplement to the UMTRA project water sampling and analysis plan, Slick Rock, Colorado

    International Nuclear Information System (INIS)

    1995-09-01

    The water sampling and analysis plan (WSAP) provides the regulatory and technical basis for ground water and surface water sampling at the Uranium Mill Tailings Remedial Action (UMTRA) Project Union Carbide (UC) and North Continent (NC) processing sites and the Burro Canyon disposal site near Slick Rock, Colorado. The initial WSAP was finalized in August 1994 and will be completely revised in accordance with the WSAP guidance document (DOE, 1995) in late 1996. This version supplements the initial WSAP, reflects only minor changes in sampling that occurred in 1995, covers sampling scheduled for early 1996, and provides a preliminary projection of the next 5 years of sampling and monitoring activities. Once surface remedial action is completed at the former processing sites, additional and more detailed hydrogeologic characterization may be needed to develop the Ground Water Program conceptual ground water model and proposed compliance strategy. In addition, background ground water quality needs to be clearly defined to ensure that the baseline risk assessment accurately estimated risks from the contaminants of potential concern in contaminated ground water at the UC and NC sites

  15. Microbiology of the surface water samples in the high background radiation areas of Ramsar, Iran

    International Nuclear Information System (INIS)

    Motamedifar, Mohammad; Zamani, Khosrow; Sedigh, Hadi; Mortazavi, Seyed Mohammad Javad; Taeb, Shahram; Haghani, M.; Mortazavi, Seyed Ali Reza; Soofi, Amir

    2014-01-01

    Residents of high background radiation areas of Ramsar have lived in these areas for many generations and received radiation doses much higher than the dose limit recommended by ICRP for radiation workers. The radioactivity of the high background radiation areas of Ramsar is reported to be due to 226 Ra and its decay products, which have been brought to the surface by the waters of hot springs. Over the past years the department has focused on different aspects of the health effects of the elevated levels of natural radiation in Ramsar. This study was aimed to perform a preliminary investigation on the bioeffects of exposure to elevated levels of natural radiation on the microbiology of surface water samples. Water samples were collected from surface water streams in Talesh Mahalleh district, Ramsar as well as a nearby area with normal levels of background radiation. Only two strains of bacteria, that is, Providencia stuartii and Shimwellia blattae, could be isolated from the water samples collected from high background radiation areas, while seven strains (Escherichia coli, Enterobacter asburiae, Klebsiella pneumoniae, Shigella dysenteriae, Buttiauxella agerstis, Tatumella punctuata and Raoultella ornithinolytica) were isolated from the water samples collected from normal background radiation areas. All the bacteria isolated from water samples of high and normal background radiation areas were sensitive to ultraviolet radiation, heat, betadine, alcohol, and deconex. Although other investigators have reported that bacteria isolated from hot springs show radioresistance, the results reported here do not reveal any adaptive response. (author)

  16. Review of robust measurement of phosphorus in river water: sampling, storage, fractionation and sensitivity

    Directory of Open Access Journals (Sweden)

    H. P. Jarvie

    2002-01-01

    Full Text Available This paper reviews current knowledge on sampling, storage and analysis of phosphorus (P in river waters. Potential sensitivity of rivers with different physical, chemical and biological characteristics (trophic status, turbidity, flow regime, matrix chemistry is examined in terms of errors associated with sampling, sample preparation, storage, contamination, interference and analytical errors. Key issues identified include: The need to tailor analytical reagents and concentrations to take into account the characteristics of the sample matrix. The effects of matrix interference on the colorimetric analysis. The influence of variable rates of phospho-molybdenum blue colour formation. The differing responses of river waters to physical and chemical conditions of storage. The higher sensitivities of samples with low P concentrations to storage and analytical errors. Given high variability of river water characteristics in space and time, no single standardised methodology for sampling, storage and analysis of P in rivers can be offered. ‘Good Practice’ guidelines are suggested, which recommend that protocols for sampling, storage and analysis of river water for P is based on thorough site-specific method testing and assessment of P stability on storage. For wider sampling programmes at the regional/national scale where intensive site-specific method and stability testing are not feasible, ‘Precautionary Practice’ guidelines are suggested. The study highlights key areas requiring further investigation for improving methodological rigour. Keywords: phosphorus, orthophosphate, soluble reactive, particulate, colorimetry, stability, sensitivity, analytical error, storage, sampling, filtration, preservative, fractionation, digestion

  17. Guidance document for preparing water sampling and analysis plans for UMTRA Project sites. Revision 1

    International Nuclear Information System (INIS)

    1995-09-01

    A water sampling and analysis plan (WSAP) is prepared for each Uranium Mill Tailings Remedial Action (UMTRA) Project site to provide the rationale for routine ground water sampling at disposal sites and former processing sites. The WSAP identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequency for the routine ground water monitoring stations at each site. This guidance document has been prepared by the Technical Assistance Contractor (TAC) for the US Department of Energy (DOE). Its purpose is to provide a consistent technical approach for sampling and monitoring activities performed under the WSAP and to provide a consistent format for the WSAP documents. It is designed for use by the TAC in preparing WSAPs and by the DOE, US Nuclear Regulatory Commission, state and tribal agencies, other regulatory agencies, and the public in evaluating the content of WSAPS

  18. Soil and Water – What is Detectable through Microbiological Sample Preparation Techniques

    Science.gov (United States)

    The concerns of a potential terrorist’s use of biological agents in soil and ground water are articulated by comparisons to major illnesses in this Country involving contaminated drinking water sources. Objectives are focused on the importance of sample preparation in the rapid, ...

  19. Analysis of trace uranium and plutonium in environmental water sample by ICP-MS

    International Nuclear Information System (INIS)

    Liu Xuemei

    2004-12-01

    The analysis of trace Uranium and Plutonium in environmental water is very important in the environment inspect. The preparation method of water samples are introduced and several common used method are compared. The analysis process and the calibration method with ICP-MS are discussed in detail considering present conditions. (author)

  20. Natural radioactivity in various water samples and radiation dose estimations in Bolu province, Turkey.

    Science.gov (United States)

    Gorur, F Korkmaz; Camgoz, H

    2014-10-01

    The level of natural radioactivity for Bolu province of north-western Turkey was assessed in this study. There is no information about radioactivity measurement reported in water samples in the Bolu province so far. For this reason, gross α and β activities of 55 different water samples collected from tap, spring, mineral, river and lake waters in Bolu were determined. The mean activity concentrations were 68.11 mBq L(-1), 169.44 mBq L(-1) for gross α and β in tap water. For all samples the gross β activity is always higher than the gross α activity. All value of the gross α were lower than the limit value of 500 mBq L(-1) while two spring and one mineral water samples were found to have gross β activity concentrations of greater than 1000 mBq L(-1). The associated age-dependent dose from all water ingestion in Bolu was estimated. The total dose for adults had an average value exceeds the WHO recommended limit value. The risk levels from the direct ingestion of the natural radionuclides in tap and mineral water in Bolu were determinated. The mean (210)Po and (228)Ra risk the value of tap and mineral waters slightly exceeds what some consider on acceptable risk of 10(-4) or less. Copyright © 2014 Elsevier Ltd. All rights reserved.

  1. Stable isotope ratio measurements on highly enriched water samples by means of laser spectrometry

    NARCIS (Netherlands)

    van Trigt, R; Kerstel, E.R.T.; Visser, GH; Meijer, H.A.J.

    2001-01-01

    We demonstrate the feasibility of using laser spectrometry (LS) to analyze isotopically highly enriched water samples (i.e., delta H-2 less than or equal to 15000 parts per thousand, delta O-18 less than or equal to 1200 parts per thousand), as often used in the biomedical doubly labeled water (DLW)

  2. Quality control on the accuracy of the total Beta activity index in different sample matrices water

    International Nuclear Information System (INIS)

    Pujol, L.; Pablo, M. A. de; Payeras, J.

    2013-01-01

    The standard ISO/IEC 17025:2005 of general requirements for the technical competence of testing and calibration laboratories, provides that a laboratory shall have quality control procedures for monitoring the validity of tests and calibrations ago. In this paper, the experience of Isotopic Applications Laboratory (CEDEX) in controlling the accuracy rate of total beta activity in samples of drinking water, inland waters and marine waters is presented. (Author)

  3. Introduction of Flame Atomic Absorption Spectrometry (FAAS) For River Water Samples Analysis

    International Nuclear Information System (INIS)

    Shakirah Abd Shukor; Mohd Suhaimi Hamzah; Shamsiah Abdul Rahman

    2015-01-01

    Metal contamination in water is a major component in the determination of water quality monitoring. In spite of the viability of several other metal ion analysis techniques for river water, atomic absorption spectroscopy (AAS) method is most commonly used due to the reproducibility results, short analysis time, cost effective, lower level detection and robust. Therefore, this article gives an overview on the principles, instrumentation techniques, sample preparations, instrument calibration and data analysis in a simple manner for beginner. (author)

  4. Qualilty, isotopes, and radiochemistry of water sampled from the Upper Moenkopi Village water-supply wells, Coconino County, Arizona

    Science.gov (United States)

    Carruth, Rob; Beisner, Kimberly; Smith, Greg

    2013-01-01

    The Hopi Tribe Water Resources Program has granted contracts for studies to evaluate water supply conditions for the Moenkopi villages in Coconino County, Arizona. The Moenkopi villages include Upper Moenkopi Village and the village of Lower Moencopi, both on the Hopi Indian Reservation south of the Navajo community of Tuba City. These investigations have determined that water supplies are limited and vulnerable to several potential sources of contamination, including the Tuba City Landfill and a former uranium processing facility known as the Rare Metals Mill. Studies are ongoing to determine if uranium and other metals in groundwater beneath the landfill are greater than regional groundwater concentrations. The source of water supply for the Upper Moenkopi Village is three public-supply wells. The wells are referred to as MSW-1, MSW-2, and MSW-3 and all three wells obtain water from the regionally extensive N aquifer. The N aquifer is the principal aquifer in this region of northern Arizona and consists of thick beds of sandstone between less permeable layers of siltstone and mudstone. The relatively fine-grained character of the N aquifer inhibits rapid movement of water and large yields to wells. In recent years, water levels have declined in the three public-supply wells, causing concern that the current water supply will not be able to accommodate peak demand and allow for residential and economic growth. Analyses of major ions, nutrients, selected trace metals, stable and radioactive isotopes, and radiochemistry were performed on the groundwater samples from the three public-supply wells to describe general water-quality conditions and groundwater ages in and immediately surrounding the Upper Moenkopi Village area. None of the water samples collected from the public-supply wells exceeded the U.S. Environmental Protection Agency primary drinking water standards. The ratios of the major dissolved ions from the samples collected from MSW-1 and MSW-2 indicate

  5. Absolute measurement of the isotopic ratio of a water sample with very low deuterium content

    International Nuclear Information System (INIS)

    Hagemann, R.; Nief, G.; Roth, E.

    1968-01-01

    The presence of H 3+ ions which are indistinguishable from HD + ions presents the principal difficulty encountered in the measurement of isotopic ratios of water samples with very low deuterium contents using a mass spectrometer. Thus, when the sample contains no deuterium, the mass spectrometer does not indicate zero. By producing, in situ, from the sample to be measured, water vapor with an isotopic ratio very close to zero using a small distilling column, this difficulty is overcome. This column, its operating parameters, as well as the way in which the measurements are made are described. An arrangement is employed in which the isotopic ratios can be measured with a sensitivity better than 0.01 x 10 -6 . The method is applied to the determination of the isotopic ratios of three low deuterium content water samples. The results obtained permit one to assign to the sample with the lowest deuterium content an absolute value equal to 1.71 ± 0.03 ppm. This water sample is a primary standard from which is determined the isotopic ratio of a natural water sample which serves as the laboratory standard. (author) [fr

  6. Sampling

    CERN Document Server

    Thompson, Steven K

    2012-01-01

    Praise for the Second Edition "This book has never had a competitor. It is the only book that takes a broad approach to sampling . . . any good personal statistics library should include a copy of this book." —Technometrics "Well-written . . . an excellent book on an important subject. Highly recommended." —Choice "An ideal reference for scientific researchers and other professionals who use sampling." —Zentralblatt Math Features new developments in the field combined with all aspects of obtaining, interpreting, and using sample data Sampling provides an up-to-date treat

  7. Physicochemical transformation and algal toxicity of engineered nanoparticles in surface water samples

    International Nuclear Information System (INIS)

    Zhang, Luqing; Li, Jingyi; Yang, Kun; Liu, Jingfu; Lin, Daohui

    2016-01-01

    Most studies on the behavior and toxicity of engineered nanoparticles (NPs) have been conducted in artificial water with well-controlled conditions, which are dramatically different from natural waters with complex compositions. To better understand the fate and toxicity of NPs in the natural water environment, physicochemical transformations of four NPs (TiO_2, ZnO, Ag, and carbon nanotubes (CNTs)) and their toxicities towards a unicellular green alga (Chlorella pyrenoidosa) in four fresh water and one seawater sample were investigated. Results indicated that water chemistry had profound effects on aggregation, dissolution, and algal toxicity of the NPs. The strongest homoaggregation of the NPs was associated with the highest ionic strength, but no obvious correlation was observed between the homoaggregation of NPs and pH or dissolved organic matter content of the water samples. The greatest dissolution of ZnO NPs also occurred in seawater with the highest ionic strength, while the dissolution of Ag NPs varied differently from ZnO NPs. The released Zn"2"+ and especially Ag"+ mainly accounted for the algal toxicity of ZnO and Ag NPs, respectively. The NP-cell heteroagglomeration occurred generally for CNTs and Ag NPs, which contributed to the observed nanotoxicity. However, there was no significant correlation between the observed nanotoxicity and the type of NP or the water chemistry. It was thus concluded that the physicochemical transformations and algal toxicities of NPs in the natural water samples were caused by the combined effects of complex water quality parameters rather than any single influencing factor alone. These results will increase our knowledge on the fate and effects of NPs in the aquatic environment. - Highlights: • Transformation and algal toxicity of four NPs in five surface water samples were studied. • The transformation and toxicity were dependent on the types of NPs and water samples. • No single water parameter alone was

  8. Evaluation of the Validity of Groundwater Samples Obtained Using the Purge Water Management System at SRS

    International Nuclear Information System (INIS)

    Beardsley, C.C.

    1999-01-01

    As part of the demonstration testing of the Purge Water Management System (PWMS) technology at the Savannah River Site (SRS), four wells were equipped with PWMS units in 1997 and a series of sampling events were conducted at each during 1997-1998. Three of the wells were located in A/M Area while the fourth was located at the Old Radioactive Waste Burial Ground in the General Separations Area.The PWMS is a ''closed-loop'', non-contact, system used to collect and return purge water to the originating aquifer after a sampling event without having significantly altered the water quality. One of the primary concerns as to its applicability at SRS, and elsewhere, is whether the PWMS might resample groundwater that is returned to the aquifer during the previous sampling event. The purpose of the present investigation was to compare groundwater chemical analysis data collected at the four test wells using the PWMS vs. historical data collected using the standard monitoring program methodology to determine if the PWMS provides representative monitoring samples.The analysis of the groundwater chemical concentrations indicates that the PWMS sampling methodology acquired representative groundwater samples at monitoring wells ABP-1A, ABP-4, ARP-3 and BGO-33C. Representative groundwater samples are achieved if the PWMS does not resample groundwater that has been purged and returned during a previous sampling event. Initial screening calculations, conducted prior to the selection of these four wells, indicated that groundwater velocities were high enough under the ambient hydraulic gradients to preclude resampling from occurring at the time intervals that were used at each well. Corroborating evidence included a tracer test that was conducted at BGO-33C, the high degree of similarity between analyte concentrations derived from the PWMS samples and those obtained from historical protocol sampling, as well as the fact that PWMS data extend all previously existing concentration

  9. Characterization samples of Tigris river water treated with nano colloidal silver (physically, chemically, microbiologically)

    International Nuclear Information System (INIS)

    Dumboos, H. I.; Beden, S. J.; Zouari, K.; Chkir, N.; Ahmed, H. A.

    2012-12-01

    Many researches of using nano silver in purification of drinking water from bacteria and its effect on stan dared properties as drinking water were established. Two stages accomplished in these projects. First stage include preparation of colloidal silver with characterization process and prepare water samples through sedimentation, filtration process, PH and turbidity measure then treated with colloidal silver in volume ratio (0.1-Λ) ml/100ml. The second stage represent select the better results from stage one and take samples to determine the standard characterization values with chemical, physical and microbiological taste. Results will be compared with Iraq standard certification. (Author)

  10. Determination of natural uranium, thorium and radium isotopes in water and soil samples by alpha spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Hao, Le Cong; Tao, Chau Van; Thong, Luong Van; Linh, Duong Mong [University of Science Ho Chi Minh City (Viet Nam). Faculty of Physics and Engineering Physics; Dong, Nguyen Van [University of Science Ho Chi Minh City (Viet Nam). Faculty of Chemistry

    2011-08-15

    In this study, a simple procedure for the determination of natural uranium, thorium and radium isotopes in water and soil samples by alpha spectroscopy is described. This procedure allows a sequential extraction polonium, uranium, thorium and radium radionuclides from the same sample in two to three days. It was tested and validated with the analysis of certified reference materials from the IAEA. (orig.)

  11. Use of passive sampling devices for monitoring and compliance checking of POP concentrations in water

    NARCIS (Netherlands)

    Lohmann, R.; Booij, K.; Smedes, F.; Vrana, B.

    2012-01-01

    The state of the art of passive water sampling of (nonpolar) organic contaminants is presented. Its suitability for regulatory monitoring is discussed, with an emphasis on the information yielded by passive sampling devices (PSDs), their relevance and associated uncertainties. Almost all persistent

  12. Study of the concentration of 7 Be in samples of rain water

    International Nuclear Information System (INIS)

    Quintero P, E.; Rojas M, V.P.

    2004-01-01

    This work shows the methodology carried out for the determination of 7 Be in samples of rain water and the obtained results of the concentration of having said radionuclide in this sampled matrix during the last five years in the Nuclear Center of Mexico. (Author)

  13. Study of changes in bacterial and viral abundance in formaldehyde - Fixed water samples by epifluorescence microscopy

    Digital Repository Service at National Institute of Oceanography (India)

    Parvathi, A.; Radhakrishnan, S.; Sajila, M.P.; Jacob, B.

    of bacteria and viruses in water samples from Cochin Backwater was determined by SYBR Green I staining and epifluorescence microscopy. The counts were determined for 45 days in samples fixed with 1–6% formaldehyde. The results suggest rapid decline in counts...

  14. PASSIVE SAMPLING OF GROUND WATER MONITORING WELLS WITHOUT PURGING MULTILEVEL WELL CHEMISTRY AND TRACER DISAPPEARANCE

    Science.gov (United States)

    It is essential that the sampling techniques utilized in groundwater monitoring provide data that accurately depicts the water quality of the sampled aquifer in the vicinity of the well. Due to the large amount of monitoring activity currently underway in the U.S.A. it is also im...

  15. Concentration of ions in selected bottled water samples sold in Malaysia

    Science.gov (United States)

    Aris, Ahmad Zaharin; Kam, Ryan Chuan Yang; Lim, Ai Phing; Praveena, Sarva Mangala

    2013-03-01

    Many consumers around the world, including Malaysians, have turned to bottled water as their main source of drinking water. The aim of this study is to determine the physical and chemical properties of bottled water samples sold in Selangor, Malaysia. A total of 20 bottled water brands consisting of `natural mineral (NM)' and `packaged drinking (PD)' types were randomly collected and analyzed for their physical-chemical characteristics: hydrogen ion concentration (pH), electrical conductivity (EC) and total dissolved solids (TDS), selected major ions: calcium (Ca), potassium (K), magnesium (Mg) and sodium (Na), and minor trace constituents: copper (Cu) and zinc (Zn) to ascertain their suitability for human consumption. The results obtained were compared with guideline values recommended by World Health Organization (WHO) and Malaysian Ministry of Health (MMOH), respectively. It was found that all bottled water samples were in accordance with the guidelines set by WHO and MMOH except for one sample (D3) which was below the pH limit of 6.5. Both NM and PD bottled water were dominated by Na + K > Ca > Mg. Low values for EC and TDS in the bottled water samples showed that water was deficient in essential elements, likely an indication that these were removed by water treatment. Minerals like major ions were present in very low concentrations which could pose a risk to individuals who consume this water on a regular basis. Generally, the overall quality of the supplied bottled water was in accordance to standards and guidelines set by WHO and MMOH and safe for consumption.

  16. DETERMINATION OF ORGANOCHLORINE PESTICIDES IN DRINKING WATERS SAMPLED FROM CLUJ AND HUNEDOARA COUNTIES

    Directory of Open Access Journals (Sweden)

    MARIA-ELISABETA LOVÁSZ

    2011-03-01

    Full Text Available Determination of organochlorine pesticides in drinking waterssampled from Cluj and Hunedoara counties. Pesticides are found scattered indifferent environmental factors (water, air, soil wherefrom they are drawn off byvegetal and animal organisms. Water pollution by pesticides results from the plantprotection products industry and also from massive application of these resourcesin agriculture and other branches of economy. Pesticides can reach surface wateralong with dripping waters and by infiltration may reach the groundwater layers,organochlorine pesticides are most often found in the water sources (dieldrin,endrin, DDT, aldrin, lindane, heptachlor, etc. due to their increased persistence inthe external environment. This study followed up the determination oforganochlorine pesticides in 14 drinking water samples collected from the outputof water treatment plants in Cluj and Hunedoara counties that process surfacewater and deep-water sources. For identification of organochlorine pesticides, thegas chromatographic method after liquid-liquid extraction was used, by a gascromatograph Shimadzu GC 2010 with detector ECD (Electron CaptureDetection. There were not detected higher values than the method detection limit(0.01 μg/l in the drinking water samples collected and analyzed for both totalorganochlorine pesticides and components, which were well below the maximumconcentration admitted by Law 452/2002 regarding drinking water quality. Resultsare correlated with the sanitary protection areas for water sources and with the useof agricultural lands in the area. The solution to reduce risk of pesticides use isecological agriculture , which gains increasingly more ground in Romania too.

  17. May 2011 Groundwater and Surface Water Sampling at the Rio Blanco, Colorado, Site (Data Validation Package)

    International Nuclear Information System (INIS)

    2011-01-01

    Annual sampling was conducted at the Rio Blanco, Colorado, site for the Long-Term Hydrologic Monitoring Program May 16-17, 2011, to monitor groundwater and surface water for potential radionuclide contamination. Sampling and analyses were conducted as specified in Sampling and Analysis Plan for the U.S. Department of Energy Office of Legacy Management Sites (LMS/PRO/S04351, continually updated). A duplicate sample was collected from location Johnson Artesian WL. Samples were analyzed by the U.S. Environmental Protection Agency (EPA) Radiation&Indoor Environments National Laboratory in Las Vegas, Nevada. Samples were analyzed for gamma-emitting radionuclides by high-resolution gamma spectrometry, and for tritium using the conventional method. Tritium was not measured using the enrichment method because the EPA laboratory no longer offers that service. Results of this monitoring at the Rio Blanco site demonstrate that groundwater and surface water outside the boundaries have not been affected by project-related contaminants.

  18. Performance of a hydrostatic sampler for collecting samples at the water-sediment interface in lakes

    Directory of Open Access Journals (Sweden)

    Fernando PEDROZO

    2008-02-01

    Full Text Available The water-sediment interface plays a significant role in the determination of the trophic degree of a waterbody. Numerous redox reactions take place there, resulting in the release of contaminants from the sediments to the water column. The aim of the present work was to develop an equipment for collecting samples from the water-sediment interface. Such equipment was to have a simple design, low construction cost, no depth limitations, and high levels of personal safety and to be reliable in the collection of samples. The performance of the hydrostatic sampler thus developed was tested against samples collected either remotely with a corer or directly with syringes by autonomous divers. The hydrostatic sampler permits access to depths where the costs of the traditional diving methodology are expensive, and where working conditions are dangerous for the diver. The hydrostatic sampler provides an additional means of collecting samples from the water-sediment interface, which together with pore-water samples, facilitates the investigation and understanding of chemical mechanisms in lakes, for instance, those that control the P release from sediment to the water column.

  19. [Detecting Thallium in Water Samples using Dispersive Liquid Phase Microextraction-Graphite Furnace Atomic Absorption Spectroscopy].

    Science.gov (United States)

    Zhu, Jing; Li, Yan; Zheng, Bo; Tang, Wei; Chen, Xiao; Zou, Xiao-li

    2015-11-01

    To develope a method of solvent demulsification dispersive liquid phase microextraction (SD-DLPME) based on ion association reaction coupled with graphite furnace atomic absorption spectroscopy (GFAAS) for detecting thallium in water samples. Methods Thallium ion in water samples was oxidized to Tl(III) with bromine water, which reacted with Cl- to form TlCl4-. The ionic associated compound with trioctylamine was obtained and extracted. DLPME was completed with ethanol as dispersive solvent. The separation of aqueous and organic phase was achieved by injecting into demulsification solvent without centrifugation. The extractant was collected and injected into GFAAS for analysis. With palladium colloid as matrix modifier, a two step drying and ashing temperature programming process was applied for high precision and sensitivity. The linear range was 0.05-2.0 microg/L, with a detection limit of 0.011 microg/L. The relative standard derivation (RSD) for detecting Tl in spiked water sample was 9.9%. The spiked recoveries of water samples ranged from 94.0% to 103.0%. The method is simple, sensitive and suitable for batch analysis of Tl in water samples.

  20. White HDPE bottles as source of serious contamination of water samples with Ba and Zn.

    Science.gov (United States)

    Reimann, Clemens; Grimstvedt, Andreas; Frengstad, Bjørn; Finne, Tor Erik

    2007-03-15

    During a recent study of surface water quality factory new white high-density polyethylene (HDPE) bottles were used for collecting the water samples. According to the established field protocol of the Geological Survey of Norway the bottles were twice carefully rinsed with water in the field prior to sampling. Several blank samples using milli-Q (ELGA) water (>18.2 MOmega) were also prepared. On checking the analytical results the blanks returned values of Ag, Ba, Sr, V, Zn and Zr. For Ba and Zn the values (c. 300 microg/l and 95 microg/l) were about 10 times above the concentrations that can be expected in natural waters. A laboratory test of the bottles demonstrated that the bottles contaminate the samples with significant amounts of Ba and Zn and some Sr. Simple acid washing of the bottles prior to use did not solve the contamination problem for Ba and Zn. The results suggest that there may exist "clean" and "dirty" HDPE bottles depending on manufacturer/production process. When collecting water samples it is mandatory to check bottles regularly as a possible source of contamination.

  1. Effects of sterilization treatments on the analysis of TOC in water samples.

    Science.gov (United States)

    Shi, Yiming; Xu, Lingfeng; Gong, Dongqin; Lu, Jun

    2010-01-01

    Decomposition experiments conducted with and without microbial processes are commonly used to study the effects of environmental microorganisms on the degradation of organic pollutants. However, the effects of biological pretreatment (sterilization) on organic matter often have a negative impact on such experiments. Based on the principle of water total organic carbon (TOC) analysis, the effects of physical sterilization treatments on determination of TOC and other water quality parameters were investigated. The results revealed that two conventional physical sterilization treatments, autoclaving and 60Co gamma-radiation sterilization, led to the direct decomposition of some organic pollutants, resulting in remarkable errors in the analysis of TOC in water samples. Furthermore, the extent of the errors varied with the intensity and the duration of sterilization treatments. Accordingly, a novel sterilization method for water samples, 0.45 microm micro-filtration coupled with ultraviolet radiation (MCUR), was developed in the present study. The results indicated that the MCUR method was capable of exerting a high bactericidal effect on the water sample while significantly decreasing the negative impact on the analysis of TOC and other water quality parameters. Before and after sterilization treatments, the relative errors of TOC determination could be controlled to lower than 3% for water samples with different categories and concentrations of organic pollutants by using MCUR.

  2. Set Up of an Automatic Water Quality Sampling System in Irrigation Agriculture

    Directory of Open Access Journals (Sweden)

    Emanuel Heinz

    2013-12-01

    Full Text Available We have developed a high-resolution automatic sampling system for continuous in situ measurements of stable water isotopic composition and nitrogen solutes along with hydrological information. The system facilitates concurrent monitoring of a large number of water and nutrient fluxes (ground, surface, irrigation and rain water in irrigated agriculture. For this purpose we couple an automatic sampling system with a Wavelength-Scanned Cavity Ring Down Spectrometry System (WS-CRDS for stable water isotope analysis (δ2H and δ18O, a reagentless hyperspectral UV photometer (ProPS for monitoring nitrate content and various water level sensors for hydrometric information. The automatic sampling system consists of different sampling stations equipped with pumps, a switch cabinet for valve and pump control and a computer operating the system. The complete system is operated via internet-based control software, allowing supervision from nearly anywhere. The system is currently set up at the International Rice Research Institute (Los Baños, The Philippines in a diversified rice growing system to continuously monitor water and nutrient fluxes. Here we present the system’s technical set-up and provide initial proof-of-concept with results for the isotopic composition of different water sources and nitrate values from the 2012 dry season.

  3. Determination of total alpha index in samples of see water by coprecipitation method

    International Nuclear Information System (INIS)

    Suarez-Navarro, J.A.; Pujol, L.; Pozuelo, M.; Pablo, A. de

    1998-01-01

    An environmental radiological monitoring network in the Spanish sea waters was set up by CEDEX in 1993. Water radioactivity is determined quarterly in eleven sampling points along the Spanish coast. The gross alpha activity is one of the parameters to be determined. The usual method for monitoring the gross alpha activity includes sample evaporation to dryness on a disk and counting using ZnS(Ag) scintillation detector. Nevertheless, the gross alpha activity determination in saline waters, such as sea waters, is troublesome, because mass attenuation is high and a very small of water is needed (0.2 ml). The coprecipitation method allows to analyze 500 ml water samples, so the detection limit is reduced and sensitivity is improved. In this work, the coprecipitation method was used to determine the gross alpha activity in the radiological network of the Spanish coast sea waters during 1996 and 1997. Gross alpha activity was very homogenous. It averaged 0.0844±0.0086 Bq.1''1 and ranged from 0.062 to 0.102 Bq.1''1. In collaboration with CIEMAT a set of samples was analyzed, they averaged 0.0689±0.0074 Bq.1''1 and ranged from 0.056 to 0.082 Bq.1''1. (Author) 5 refs

  4. A rapid and sensitive analytical method for the determination of 14 pyrethroids in water samples.

    Science.gov (United States)

    Feo, M L; Eljarrat, E; Barceló, D

    2010-04-09

    A simple, efficient and environmentally friendly analytical methodology is proposed for extracting and preconcentrating pyrethroids from water samples prior to gas chromatography-negative ion chemical ionization mass spectrometry (GC-NCI-MS) analysis. Fourteen pyrethroids were selected for this work: bifenthrin, cyfluthrin, lambda-cyhalothrin, cypermethrin, deltamethrin, esfenvalerate, fenvalerate, fenpropathrin, tau-fluvalinate, permethrin, phenothrin, resmethrin, tetramethrin and tralomethrin. The method is based on ultrasound-assisted emulsification-extraction (UAEE) of a water-immiscible solvent in an aqueous medium. Chloroform was used as extraction solvent in the UAEE technique. Target analytes were quantitatively extracted achieving an enrichment factor of 200 when 20 mL aliquot of pure water spiked with pyrethroid standards was extracted. The method was also evaluated with tap water and river water samples. Method detection limits (MDLs) ranged from 0.03 to 35.8 ng L(-1) with RSDs values or =0.998. Recovery values were in the range of 45-106%, showing satisfactory robustness of the method for analyzing pyrethroids in water samples. The proposed methodology was applied for the analysis of river water samples. Cypermethrin was detected at concentration levels ranging from 4.94 to 30.5 ng L(-1). Copyright 2010 Elsevier B.V. All rights reserved.

  5. Water-quality assessment of south-central Texas : comparison of water quality in surface-water samples collected manually and by automated samplers

    Science.gov (United States)

    Ging, Patricia B.

    1999-01-01

    Surface-water sampling protocols of the U.S. Geological Survey National Water-Quality Assessment (NAWQA) Program specify samples for most properties and constituents to be collected manually in equal-width increments across a stream channel and composited for analysis. Single-point sampling with an automated sampler (autosampler) during storms was proposed in the upper part of the South-Central Texas NAWQA study unit, raising the question of whether property and constituent concentrations from automatically collected samples differ significantly from those in samples collected manually. Statistical (Wilcoxon signed-rank test) analyses of 3 to 16 paired concentrations for each of 26 properties and constituents from water samples collected using both methods at eight sites in the upper part of the study unit indicated that there were no significant differences in concentrations for dissolved constituents, other than calcium and organic carbon.

  6. Determination of radiocaesium in agriculture-related water samples containing suspended solids using gelling method

    International Nuclear Information System (INIS)

    Matsunami, Hisaya; Shin, Moono; Takahashi, Yoshihiko; Shinano, Takuro; Kitajima, Shiori; Tsuchiya, Takashi

    2015-01-01

    After the TEPCO Fukushima Dai-ichi Nuclear Power Plant accident in 2011, the radiocaesium, which flowed into the paddy fields via irrigation water, have been widely investigated. When the concentration of radiocaesium in the water samples containing suspended solids were directly measured using a high purity germanium detector with a 2 L marinelli beaker, the radiocaesium concentration might be overestimated due to the sedimentation of the suspended solids during the measurement time. In fact, the values obtained by the direct method were higher than those obtained by the filtering method and/or the gelling method in most of the agriculture-related water samples. We concluded that the gelling method using sodium polyacrylate can be widely adapted for the analysis of the total radiocaesium in the agriculture-related water samples because of its many advantage such as simple preparation procedure, accurate analysis values, excellent long-term stability of geometry and low operating cost. (author)

  7. Analysis of bromate in drinking water using liquid chromatography-tandem mass spectrometry without sample pretreatment.

    Science.gov (United States)

    Kosaka, Koji; Asami, Mari; Takei, Kanako; Akiba, Michihiro

    2011-01-01

    An analytical method for determining bromate in drinking water was developed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The (18)O-enriched bromate was used as an internal standard. The limit of quantification (LOQ) of bromate was 0.2 µg/L. The peak of bromate was separated from those of coexisting ions (i.e., chloride, nitrate and sulfate). The relative and absolute recoveries of bromate in two drinking water samples and in a synthesized ion solution (100 mg/L chloride, 10 mg N/L nitrate, and 100 mg/L sulfate) were 99-105 and 94-105%, respectively. Bromate concentrations in 11 drinking water samples determined by LC-MS/MS were water without sample pretreatment.

  8. May 2013 Groundwater and Surface Water Sampling at the Rio Blanco, Colorado, Site (Data Validation Package)

    Energy Technology Data Exchange (ETDEWEB)

    Hutton, Rick [S.M. Stoller Corporation, Broomfield, CO (United States)

    2013-10-01

    Annual sampling was conducted at the Rio Blanco, Colorado, site for the Long-Term Hydrologic Monitoring Program May 14-16, 2013, to monitor groundwater and surface water for potential radionuclide contamination. Sampling and analyses were conducted as specified in Sampling and Analysis Plan for the U.S. Department of Energy Office of Legacy Management Sites (LMS/PRO/S04351, continually updated). A duplicate sample was collected from location CER #1 Black Sulphur. Samples were analyzed for gamma-emitting radionuclides by high-resolution gamma spectrometry and for tritium using the conventional and enrichment methods.

  9. Research on How to Remove Efficiently the Condensate Water of Sampling System

    International Nuclear Information System (INIS)

    Cho, SungHwan; Kim, MinSoo; Choi, HoYoung; In, WonHo

    2015-01-01

    Corrosion was caused in the measurement chamber inside the O 2 and H 2 analyzer, and thus measuring the concentration of O 2 and H 2 was not possible. It was confirmed that the cause of the occurrence of condensate water is due to the temperature difference caused during the process of the internal gas of the disposal and degasifier tank being brought into the analyzer. Thus, a heating system was installed inside and outside of the sampling panel for gas to remove generated condensate water in the analyzer and pipe. For the case where condensate water is not removed by the heating system, drain port is also installed in the sampling panel for gas to collect the condensate water of the sampling system. It was verified that there is a great volume of condensate water existing in the pipe line during the purging process after installing manufactured goods. The condensate water was fully removed by the installed heating cable and drain port. The heating cable was operated constantly at a temperature of 80 to 90 .deg. C, which allows the precise measurement of gas concentration and longer maintenance duration by blocking of the condensate water before being produced. To install instruments for measuring the gas, such as an O 2 and H 2 analyzer etc., consideration regarding whether there condensate water is present due to the temperature difference between the measuring system and analyzer is required

  10. Research on How to Remove Efficiently the Condensate Water of Sampling System

    Energy Technology Data Exchange (ETDEWEB)

    Cho, SungHwan; Kim, MinSoo; Choi, HoYoung; In, WonHo [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2015-10-15

    Corrosion was caused in the measurement chamber inside the O{sub 2} and H{sub 2} analyzer, and thus measuring the concentration of O{sub 2} and H{sub 2} was not possible. It was confirmed that the cause of the occurrence of condensate water is due to the temperature difference caused during the process of the internal gas of the disposal and degasifier tank being brought into the analyzer. Thus, a heating system was installed inside and outside of the sampling panel for gas to remove generated condensate water in the analyzer and pipe. For the case where condensate water is not removed by the heating system, drain port is also installed in the sampling panel for gas to collect the condensate water of the sampling system. It was verified that there is a great volume of condensate water existing in the pipe line during the purging process after installing manufactured goods. The condensate water was fully removed by the installed heating cable and drain port. The heating cable was operated constantly at a temperature of 80 to 90 .deg. C, which allows the precise measurement of gas concentration and longer maintenance duration by blocking of the condensate water before being produced. To install instruments for measuring the gas, such as an O{sub 2} and H{sub 2} analyzer etc., consideration regarding whether there condensate water is present due to the temperature difference between the measuring system and analyzer is required.

  11. Concentration of polycyclic aromatic hydrocarbons in water samples from different stages of treatment

    Directory of Open Access Journals (Sweden)

    Pogorzelec Marta

    2017-01-01

    Full Text Available The aim of this study was to analyze the presence and concentration of selected polycyclic aromatic hydrocarbons in water samples from different stages of treatment and to verify the usefulness of semipermeable membrane devices for analysis of drinking water. For this purpose, study was conducted for a period of 5 months. Semipermeable membrane devices were deployed in a surface water treatment plant located in Lower Silesia (Poland. To determine the effect of water treatment on concentration of PAHs, three sampling places were chosen: raw water input, stream of water just before disinfection and treated water output. After each month of sampling SPMDs were changed for fresh ones and prepared for further analysis. Concentrations of fifteen polycyclic aromatic hydrocarbons were determined by high performance liquid chromatography (HPLC. Presented study indicates that the use of semipermeable membrane devices can be an effective tool for the analysis of aquatic environment, including monitoring of drinking water, where organic micropollutants are present at very low concentrations.

  12. Drinking Water Quality Forecast of Peshawar Valley on the Basis of Sample Data

    International Nuclear Information System (INIS)

    Khan, S.U.; Bangash, F.K.

    2001-01-01

    Microbiological and related parameters of 75 portable water samples collected from source, distribution line and consumer tap in 25 different locations were investigated. The findings were used to forecast statistically the quality of drinking water of hole valley at all three sites and compared with WHO's standards. The study shows that the valley has good water deposits and suitable for drinking purposes however the same quality is not maintained throughout the distribution systems. The presence of total and fecal coliform in the samples collected from distribution line and consumer tap shows the mixing of wastewater through leaky joints and corroded underground supply system. The study also shows poor disinfecting practices in the study area. On the basis of this study we can say that the area got excellent subsoil water deposits but most of the consumers are supplied with water not fit for drinking purposes which is the main cause of Heath problems in the area. (author)

  13. Detection of protozoa in water samples by formalin/ether concentration method.

    Science.gov (United States)

    Lora-Suarez, Fabiana; Rivera, Raul; Triviño-Valencia, Jessica; Gomez-Marin, Jorge E

    2016-09-01

    Methods to detect protozoa in water samples are expensive and laborious. We evaluated the formalin/ether concentration method to detect Giardia sp., Cryptosporidium sp. and Toxoplasma in water. In order to test the properties of the method, we spiked water samples with different amounts of each protozoa (0, 10 and 50 cysts or oocysts) in a volume of 10 L of water. Immunofluorescence assay was used for detection of Giardia and Cryptosporidium. Toxoplasma oocysts were identified by morphology. The mean percent of recovery in 10 repetitions of the entire method, in 10 samples spiked with ten parasites and read by three different observers, were for Cryptosporidium 71.3 ± 12, for Giardia 63 ± 10 and for Toxoplasma 91.6 ± 9 and the relative standard deviation of the method was of 17.5, 17.2 and 9.8, respectively. Intraobserver variation as measured by intraclass correlation coefficient, was fair for Toxoplasma, moderate for Cryptosporidium and almost perfect for Giardia. The method was then applied in 77 samples of raw and drinkable water in three different plant of water treatment. Cryptosporidium was found in 28 of 77 samples (36%) and Giardia in 31 of 77 samples (40%). Theses results identified significant differences in treatment process to reduce the presence of Giardia and Cryptosporidium. In conclusion, the formalin ether method to concentrate protozoa in water is a new alternative for low resources countries, where is urgently need to monitor and follow the presence of theses protozoa in drinkable water. Copyright © 2016 Elsevier Ltd. All rights reserved.

  14. Effects of soil water saturation on sampling equilibrium and kinetics of selected polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Kim, Pil-Gon; Roh, Ji-Yeon; Hong, Yongseok; Kwon, Jung-Hwan

    2017-10-01

    Passive sampling can be applied for measuring the freely dissolved concentration of hydrophobic organic chemicals (HOCs) in soil pore water. When using passive samplers under field conditions, however, there are factors that might affect passive sampling equilibrium and kinetics, such as soil water saturation. To determine the effects of soil water saturation on passive sampling, the equilibrium and kinetics of passive sampling were evaluated by observing changes in the distribution coefficient between sampler and soil (K sampler/soil ) and the uptake rate constant (k u ) at various soil water saturations. Polydimethylsiloxane (PDMS) passive samplers were deployed into artificial soils spiked with seven selected polycyclic aromatic hydrocarbons (PAHs). In dry soil (0% water saturation), both K sampler/soil and k u values were much lower than those in wet soils likely due to the contribution of adsorption of PAHs onto soil mineral surfaces and the conformational changes in soil organic matter. For high molecular weight PAHs (chrysene, benzo[a]pyrene, and dibenzo[a,h]anthracene), both K sampler/soil and k u values increased with increasing soil water saturation, whereas they decreased with increasing soil water saturation for low molecular weight PAHs (phenanthrene, anthracene, fluoranthene, and pyrene). Changes in the sorption capacity of soil organic matter with soil water content would be the main cause of the changes in passive sampling equilibrium. Henry's law constant could explain the different behaviors in uptake kinetics of the selected PAHs. The results of this study would be helpful when passive samplers are deployed under various soil water saturations. Copyright © 2017 Elsevier Ltd. All rights reserved.

  15. Effects of physical and chemical heterogeneity on water-quality samples obtained from wells

    Science.gov (United States)

    Reilly, Thomas E.; Gibs, Jacob

    1993-01-01

    Factors that affect the mass of chemical constituents entering a well include the distributions of flow rate and chemical concentrations along and near the screened or open section of the well. Assuming a layered porous medium (with each layer being characterized by a uniform hydraulic conductivity and chemical concentration), a knowledge of the flow from each layer along the screened zone and of the chemical concentrations in each layer enables the total mass entering the well to be determined. Analyses of hypothetical systems and a site at Galloway, NJ, provide insight into the temporal variation of water-quality data observed when withdrawing water from screened wells in heterogeneous ground-water systems.The analyses of hypothetical systems quantitatively indicate the cause-and-effect relations that cause temporal variability in water samples obtained from wells. Chemical constituents that have relatively uniform concentrations with depth may not show variations in concentrations in the water discharged from a well after the well is purged (evacuation of standing water in the well casing). However, chemical constituents that do not have uniform concentrations near the screened interval of the well may show variations in concentrations in the well discharge water after purging because of the physics of ground-water flow in the vicinity of the screen.Water-quality samples were obtained through time over a 30 minute period from a site at Galloway, NJ. The water samples were analyzed for aromatic hydrocarbons, and the data for benzene, toluene, and meta+para xylene were evaluated for temporal variations. Samples were taken from seven discrete zones, and the flow-weighted concentrations of benzene, toluene, and meta+para xylene all indicate an increase in concentration over time during pumping. These observed trends in time were reproduced numerically based on the estimated concentration distribution in the aquifer and the flow rates from each zone.The results of

  16. Trace element analysis of mineral water samples by PIXE and ICP-MS

    International Nuclear Information System (INIS)

    Kennedy, V.John; Augusthy, A.; Varier, K. M.; Magudapathy, P.; Panchapakesan, S.; Nair, K.G.M.

    1998-01-01

    Trace elements present in bottled mineral water have been studied by PIXE and ICP-MS. Samples from ten different brands of brands of bottled mineral water were prepared by preconcentration techniques. Measurements were carried out using the 2 MeV proton beam obtained from 3 MV Tandem pelletron accelerator at the Institute of Physics, Bhubaneswar. Our results are compared with Indian standard packaged natural mineral water specifications, World Health Organisation (WHO) and European guidelines for drinking water standards. Concentration of aluminum was found to be more in one of the brands. In general, our results are comparable to the above standards. (author)

  17. Concentration and characteristics of depleted uranium in biological and water samples collected in Bosnia and Herzegovina

    International Nuclear Information System (INIS)

    Jia Guogang; Belli, Maria; Sansone, Umberto; Rosamilia, Silvia; Gaudino, Stefania

    2006-01-01

    During Balkan conflicts in 1994-1995, depleted uranium (DU) ordnance was employed and was left in the battlefield. Health concern is related to the risk arising from contamination of the environment with DU penetrators and dust. In order to evaluate the impact of DU on the environment and population in Bosnia and Herzegovina, radiological survey of DU in biological and water samples were carried out over the period 12-24 October 2002. The uranium isotopic concentrations in biological samples collected in Bosnia and Herzegovina, mainly lichens, mosses and barks, were found to be in the range of 0.27-35.7 Bq kg -1 for 238 U, 0.24-16.8 Bq kg -1 for 234 U, and 0.02-1.11 Bq kg -1 for 235 U, showing uranium levels to be higher than in the samples collected at the control site. Moreover, the 236 U in some of the samples was detectable. The isotopic ratios of 234 U/ 238 U showed DU to be detectable in many biological samples at most sites examined, but in very low levels. The presence of DU in the biological samples was as a result of DU contamination in air. The uranium concentrations in water samples collected in Bosnia and Herzegovina were found to be in the range of 0.27-16.2 mBq l -1 for 238 U, 0.41-15.6 mBq l -1 for 234 U and 0.012-0.695 mBq l -1 for 235 U, and two water samples were observed to be DU positive; these values are much lower than those in mineral water found in central Italy and below the WHO guideline for public drinking water. From radiotoxicological point of view, at this moment there is no significant radiological risk related to these investigated sites in terms of possible DU contamination of water and/or plants

  18. Locations of Sampling Stations for Water Quality Monitoring in Water Distribution Networks.

    Science.gov (United States)

    Rathi, Shweta; Gupta, Rajesh

    2014-04-01

    Water quality is required to be monitored in the water distribution networks (WDNs) at salient locations to assure the safe quality of water supplied to the consumers. Such monitoring stations (MSs) provide warning against any accidental contaminations. Various objectives like demand coverage, time for detection, volume of water contaminated before detection, extent of contamination, expected population affected prior to detection, detection likelihood and others, have been independently or jointly considered in determining optimal number and location of MSs in WDNs. "Demand coverage" defined as the percentage of network demand monitored by a particular monitoring station is a simple measure to locate MSs. Several methods based on formulation of coverage matrix using pre-specified coverage criteria and optimization have been suggested. Coverage criteria is defined as some minimum percentage of total flow received at the monitoring stations that passed through any upstream node included then as covered node of the monitoring station. Number of monitoring stations increases with the increase in the value of coverage criteria. Thus, the design of monitoring station becomes subjective. A simple methodology is proposed herein which priority wise iteratively selects MSs to achieve targeted demand coverage. The proposed methodology provided the same number and location of MSs for illustrative network as an optimization method did. Further, the proposed method is simple and avoids subjectivity that could arise from the consideration of coverage criteria. The application of methodology is also shown on a WDN of Dharampeth zone (Nagpur city WDN in Maharashtra, India) having 285 nodes and 367 pipes.

  19. Ground-water sampling of the NNWSI (Nevada Nuclear Waste Storage Investigation) water table test wells surrounding Yucca Mountain, Nevada

    International Nuclear Information System (INIS)

    Matuska, N.A.

    1988-12-01

    The US Geological Survey (USGS), as part of the Nevada Nuclear Waste Storage Investigation (NNWSI) study of the water table in the vicinity of Yucca Mountain, completed 16 test holes on the Nevada Test Site and Bureau of Land Management-administered lands surrounding Yucca Mountain. These 16 wells are monitored by the USGS for water-level data; however, they had not been sampled for ground-water chemistry or isotropic composition. As part of the review of the proposed Yucca Mountain high-level nuclear waste repository, the Desert Research Institute (DRI) sampled six of these wells. The goal of this sampling program was to measure field-dependent parameters of the water such as electrical conductivity, pH, temperature and dissolved oxygen, and to collect samples for major and minor element chemistry and isotopic analysis. This information will be used as part of a program to geochemically model the flow direction between the volcanic tuff aquifers and the underlying regional carbonate aquifer

  20. Characterization of Listeria monocytogenes isolated from Ganges water, human clinical and milk samples at Varanasi, India.

    Science.gov (United States)

    Soni, Dharmendra K; Singh, Rakesh K; Singh, Durg V; Dubey, Suresh K

    2013-03-01

    Listeria monocytogenes isolated from Ganges water, human clinical and milk samples were characterized by antibiotic susceptibility, serotype identification, detection of virulence genes and ERIC- and REP-PCR fingerprint analyses. All isolates were uniformly resistant to ampicillin, except two isolates, and showed variable resistance to gentamicin, cotrimoxazole, ofloxacin, rifampicin and tetracycline. Of the 20 isolates found positive for pathogens, seven (four human and three water isolates) belong to serogroups 4b, 4d and 4e; six (one human and five water isolates) belong to serogroups 1/2c and 3c; four milk isolates belong to serogroups 1/2b and 3b; and three milk isolates belong to serogroups 1/2a and 3a. Two water isolates, all human isolates, except one (Pb1) lacking inlJ gene, and three milk isolates possess inlA, inlC, plcA, prfA, actA, hlyA and iap genes. The remaining water and milk isolates showed variable presence of inlJ, plcA, prfA, and iap genes. ERIC- and REP-PCR based analyses collectively indicated that isolates of human clinical samples belong to identical or similar clone and isolates of water and milk samples belong to different clones. Overall study demonstrates the prevalence of pathogenic L. monocytogenes species in the environmental and clinical samples. Most of the isolates were resistant to commonly used antibiotics. Copyright © 2012 Elsevier B.V. All rights reserved.

  1. Relationship of land use to water quality in the Chesapeake Bay region. [water sampling and photomapping river basins

    Science.gov (United States)

    Correll, D. L.

    1978-01-01

    Both the proportions of the various land use categories present on each watershed and the specific management practices in use in each category affect the quality of runoff waters, and the water quality of the Bay. Several permanent and portable stations on various Maryland Rivers collect volume-integrated water samples. All samples are analyzed for a series of nutrient, particulate, bacterial, herbicide, and heavy metal parameters. Each basin is mapped with respect to land use by the analysis of low-elevation aerial photos. Analyses are verified and adjusted by ground truth surveys. Data are processed and stored in the Smithsonian Institution data bank. Land use categories being investigated include forests/old fields, pastureland, row crops, residential areas, upland swamps, and tidal marshes.

  2. 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.

  3. A confirmatory holding time study for purgeable VOCs in water samples

    International Nuclear Information System (INIS)

    West, O.R.; Bayne, C.K.; Siegrist, R.L.; Holden, W.H.; Bottrell, D.W.

    1996-01-01

    Analyte stability during pre-analytical storage is essential to the accurate quantification contaminants in environmental samples. This is particularly true for volatile organic compounds (VOCS) which can easily volatilize and/or degrade during sample storage. Recognizing this, regulatory agencies require water samples be collected in vials without headspace and stored at 4 degrees C, and that analyses be conducted within 14 days, 2048 even if samples are acid-preserved. Since the selection of a 14-day holding time was largely arbitrary, the appropriateness of this requirement must be re-evaluated. The goal of the study described here was to provide regulatory agencies with the necessary data to extend the maximum holding time for properly preserved VOC water samples to 28 days

  4. May 2012 Groundwater and Surface Water Sampling at the Rio Blanco, Colorado, Site (Data Validation Package)

    International Nuclear Information System (INIS)

    2012-01-01

    Annual sampling was conducted at the Rio Blanco, Colorado, site for the Long-Term Hydrologic Monitoring Program May 9-10, 2012, to monitor groundwater and surface water for potential radionuclide contamination. Sampling and analyses were conducted as specified in Sampling and Analysis Plan for the U.S. Department of Energy Office of Legacy Management Sites (LMS/PRO/S04351, continually updated). A duplicate sample was collected from location Johnson Artesian WL. Samples were analyzed for gamma-emitting radionuclides by high-resolution gamma spectrometry and for tritium using the conventional and enrichment methods. Results of this monitoring at the Rio Blanco site demonstrate that groundwater and surface water outside the site boundaries have not been affected by project-related contaminants.

  5. Preconcentration and determination of heavy metals in water, sediment and biological samples

    Directory of Open Access Journals (Sweden)

    Shirkhanloo Hamid

    2011-01-01

    Full Text Available In this study, a simple, sensitive and accurate column preconcentration method was developed for the determination of Cd, Cu and Pb ions in river water, urine and sediment samples by flame atomic absorption spectrometry. The procedure is based on the retention of the analytes on a mixed cellulose ester membrane (MCEM column from buffered sample solutions and then their elution from the column with nitric acid. Several parameters, such as pH of the sample solution, volume of the sample and eluent and flow rates of the sample were evaluated. The effects of diverse ions on the preconcentration were also investigated. The recoveries were >95 %. The developed method was applied to the determination of trace metal ions in river water, urine and sediment samples, with satisfactory results. The 3δ detection limits for Cu, Pb and Cd were found to be 2, 3 and 0.2 μg dm−3, respectively. The presented procedure was successfully applied for determination of the copper, lead and cadmium contents in real samples, i.e., river water and biological samples.

  6. [Optimization of solid-phase extraction for enrichment of toxic organic compounds in water samples].

    Science.gov (United States)

    Zhang, Ming-quan; Li, Feng-min; Wu, Qian-yuan; Hu, Hong-ying

    2013-05-01

    A concentration method for enrichment of toxic organic compounds in water samples has been developed based on combined solid-phase extraction (SPE) to reduce impurities and improve recoveries of target compounds. This SPE method was evaluated in every stage to identify the source of impurities. Based on the analysis of Waters Oasis HLB without water samples, the eluent of SPE sorbent after dichloromethane and acetone contributed 85% of impurities during SPE process. In order to reduce the impurities from SPE sorbent, soxhlet extraction of dichloromethane followed by acetone and lastly methanol was applied to the sorbents for 24 hours and the results had proven that impurities were reduced significantly. In addition to soxhlet extraction, six types of prevalent SPE sorbents were used to absorb 40 target compounds, the lgK(ow) values of which were within the range of 1.46 and 8.1, and recovery rates were compared. It was noticed and confirmed that Waters Oasis HLB had shown the best recovery results for most of the common testing samples among all three styrenedivinylbenzene (SDB) polymer sorbents, which were 77% on average. Furthermore, Waters SepPak AC-2 provided good recovery results for pesticides among three types of activated carbon sorbents and the average recovery rates reached 74%. Therefore, Waters Oasis HLB and Waters SepPak AC-2 were combined to obtain a better recovery and the average recovery rate for the tested 40 compounds of this new SPE method was 87%.

  7. Comparison of POCIS passive samplers vs. composite water sampling: A case study.

    Science.gov (United States)

    Criquet, Justine; Dumoulin, David; Howsam, Michael; Mondamert, Leslie; Goossens, Jean-François; Prygiel, Jean; Billon, Gabriel

    2017-12-31

    The relevance of Polar Organic Chemical Integrative Samplers (POCIS) was evaluated for the assessment of concentrations of 46 pesticides and 19 pharmaceuticals in a small, peri-urban river with multi-origin inputs. Throughout the period of POCIS deployment, 24h-average water samples were collected automatically, and showed the rapid temporal evolution of concentrations of several micropollutants, as well as permitting the calculation of average concentrations in the water phase for comparison with those estimated from POCIS passive samplers. In the daily water samples, cyproconazol, epoxyconazol and imidacloprid showed high temporal variations with concentrations ranging from under the limit of detection up to several hundreds of ngL -1 . Erythromycin, cyprofloxacin and iopromide also increased rapidly up to tens of ngL -1 within a few days. Conversely, atrazine, caffeine, diclofenac, and to a lesser extent carbamazepine and sucralose, were systematically present in the water samples and showed limited variation in concentrations. For most of the substances studied here, the passive samplers gave reliable average concentrations between the minimal and maximal daily concentrations during the time of deployment. For pesticides, a relatively good correlation was clearly established (R 2 =0.89) between the concentrations obtained by POCIS and those gained from average water samples. A slight underestimation of the concentration by POCIS can be attributed to inappropriate sampling rates extracted from the literature and for our system, and new values are proposed. Considering the all data set, 75% of the results indicate a relatively good agreement between the POCIS and the average water samples concentration (values of the ratio ranging between 0,33 and 3). Note further that this agreement between these concentrations remains valid considering different sampling rates extracted from the literature. Copyright © 2017 Elsevier B.V. All rights reserved.

  8. 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.

  9. Strategies for monitoring the emerging polar organic contaminants in water with emphasis on integrative passive sampling.

    Science.gov (United States)

    Söderström, Hanna; Lindberg, Richard H; Fick, Jerker

    2009-01-16

    Although polar organic contaminants (POCs) such as pharmaceuticals are considered as some of today's most emerging contaminants few of them are regulated or included in on-going monitoring programs. However, the growing concern among the public and researchers together with the new legislature within the European Union, the registration, evaluation and authorisation of chemicals (REACH) system will increase the future need of simple, low cost strategies for monitoring and risk assessment of POCs in aquatic environments. In this article, we overview the advantages and shortcomings of traditional and novel sampling techniques available for monitoring the emerging POCs in water. The benefits and drawbacks of using active and biological sampling were discussed and the principles of organic passive samplers (PS) presented. A detailed overview of type of polar organic PS available, and their classes of target compounds and field of applications were given, and the considerations involved in using them such as environmental effects and quality control were discussed. The usefulness of biological sampling of POCs in water was found to be limited. Polar organic PS was considered to be the only available, but nevertheless, an efficient alternative to active water sampling due to its simplicity, low cost, no need of power supply or maintenance, and the ability of collecting time-integrative samples with one sample collection. However, the polar organic PS need to be further developed before they can be used as standard in water quality monitoring programs.

  10. 129I, 60Co, and 106Ru measurements on water samples from the Hanford project environs

    International Nuclear Information System (INIS)

    Brauer, F.P.; Rieck, H.G. Jr.

    1973-01-01

    Groundwater flow and contamination patterns beneath the Hanford project reservation have been studied since the early days of the project. The measurement of radioactive materials at concentrations much below those required for radiation protection are useful for tracing groundwater movement and detection of potential contamination problems before they are apt to occur. Groundwater samples from a number of wells on or near the Hanford reservation have been analyzed for 129 I by neutron activation analysis and for gamma radioactivity by low-level coincidence gamma-ray spectrometry. The major radionuclides in addition to natural radioactivity detected in the underground waters by gamma-ray spectrometry were 106 Ru and 60 Co. Local river and rain water samples were also analyzed for 129 I and long-lived radionuclides. Special sample collection methods were developed to prevent contamination of the water samples during collection. Anions travel farther than cations in underground water systems since soils are primarily cation exchangers and retain the cations. Anion exchange techniques were used in the field and the laboratory to recover the desired radionuclides. Sample sizes ranged up to several thousand liters. This paper discusses the sample collection methods,analysis methods, and results obtained. The methods used were found to provide high sensitivity for groundwater studies. (auth)

  11. Using SPMDs for monitoring hydrophobic organic compounds in urban river water in Korea compared with using conventional water grab samples

    Science.gov (United States)

    Kim, Un-Jung; Kim, Hee Young; Alvarez, David A.; Lee, In-Seok; Oh, Jeong-Eun

    2014-01-01

    We aimed to verify the effectiveness of semi-permeablemembrane devices (SPMDs) formonitoring hydrophobic organic compounds, such as polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs), that are not easy to detect using conventional grab samples (because of their low concentrations), in water.We used SPMDs and grab samples to monitor PCBs and PBDEs upstream and downstream of a sewage treatment plant (STP) in the Suyeong River in Busan, Korea. Concentrations in three different phases (freely dissolved, apparently dissolved, and particulate) were measured, to investigate the aquatic fate of PCBs and PBDEs. The freely dissolved (SPMD) concentrations were 2–3 times higher than the apparently dissolved and particulate phase (grab sample) concentrations. No meaningful relationships were found between the total PCB and PBDE concentrations of the grab sample and SPMD sample because of the different partitioning behaviors and detection frequencies of the individual chemicals. However, the summed concentrations of specific PCB and PBDE congeners (that were abundant in all samples) in the grab and SPMD samples correlated well (r2 = 0.7451 for PCBs 28 + 52 + 153, r2 = 0.9987 for PBDEs 28 + 47 + 99). The PBDE concentrations measured using SPMDs decreased with increasing distance from the STP, but no apparent dilution effect was found in the grab samples. Our results show that SPMDs could be used to support grab sampling for specific chemicals, or to trace chemical sources (such as STPs) to the aquatic environment.

  12. The determination of levels of mercury, cadmium and lead in water samples from Naivasha area, Kenya

    International Nuclear Information System (INIS)

    Muigai, P.G.; Kamau, G.N.; Kinyua, A.M.

    1995-01-01

    The analysis of mercury, cadmium and lead in water samples from different environments (Lake Naivasha, River Malewa boreholes and Olkaria geothermal wells) in Naivasha region and their possible origins are reported. The levels of mercury and lead in the water samples were above the maximum permissible limits of 0.005 mg/1 and 0.1 mg/1 respectively, as stipulated by the WHO. On the other hand, 83.3% of the samples had cadmium levels above the maximum permissible limit of 0.01mg/1 in drinking water by WHO. The mercury and lead levels were also higher than those previously obtained from different regions of Kenya, while those for cadmium were within the corresponding range. Possible sources of elevated values were the geology of the surrounding area, sewage treatment works, use of phosphate rock fertilizers and lead fuels.(author)

  13. The correlation of arsenic levels in drinking water with the biological samples of skin disorders

    Energy Technology Data Exchange (ETDEWEB)

    Kazi, Tasneem Gul [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan)], E-mail: tgkazi@yahoo.com; Arain, Muhammad Balal [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan)], E-mail: bilal_ku2004@yahoo.com; Baig, Jameel Ahmed [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan)], E-mail: jab_mughal@yahoo.com; Jamali, Muhammad Khan [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan)], E-mail: mkhanjamali@yahoo.com; Afridi, Hassan Imran [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan)], E-mail: hassanimranafridi@yahoo.com; Jalbani, Nusrat [Pakistan Council for Scientific and Industrial Research, University Road Karachi-75280 (Pakistan)], E-mail: nusratjalbani_21@yahoo.com; Sarfraz, Raja Adil [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan)], E-mail: rajaadilsarfraz@gmail.com; Shah, Abdul Qadir [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan)], E-mail: aqshah07@yahoo.com; Niaz, Abdul [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan)], E-mail: niazchemist2k6@yahoo.com

    2009-01-15

    Arsenic (As) poisoning has become a worldwide public health concern. The skin is quite sensitive to As and skin lesions are the most common and earliest nonmalignant effects associated to chronic As exposure. In 2005-2007, a survey was carried out on surface and groundwater arsenic contamination and relationships between As exposure via the drinking water and related adverse health effects (melanosis and keratosis) on villagers resides on the banks of Manchar lake, southern part of Sindh, Pakistan. We screened the population from arsenic-affected villages, 61 to 73% population were identified patients suffering from chronic arsenic toxicity. The effects of As toxicity via drinking water were estimated by biological samples (scalp hair and blood) of adults (males and females), have or have not skin problem (n = 187). The referent samples of both genders were also collected from the areas having low level of As (< 10 {mu}g/L) in drinking water (n = 121). Arsenic concentration in drinking water and biological samples were analyzed using electrothermal atomic absorption spectrometry. The range of arsenic concentrations in lake surface water was 35.2-158 {mu}g/L, which is 3-15 folds higher than World Health Organization [WHO, 2004. Guidelines for drinking-water quality third ed., WHO Geneva Switzerland.]. It was observed that As concentration in the scalp hair and blood samples were above the range of permissible values 0.034-0.319 {mu}g As/g for hair and < 0.5-4.2 {mu}g/L for blood. The linear regressions showed good correlations between arsenic concentrations in water versus hair and blood samples of exposed skin diseased subjects (R{sup 2} = 0.852 and 0.718) as compared to non-diseased subjects (R{sup 2} = 0.573 and 0.351), respectively.

  14. Detection by PCR of pathogenic protozoa in raw and drinkable water samples in Colombia.

    Science.gov (United States)

    Triviño-Valencia, Jessica; Lora, Fabiana; Zuluaga, Juan David; Gomez-Marin, Jorge E

    2016-05-01

    We evaluated the presence of DNA of Giardia, Toxoplasma, and Cryptosporidium by PCR, and of Giardia and Cryptosporidium genera by immunofluorescence antibody test (IFAT), in water samples, before, during, and after plant treatment for drinkable water. We applied this method in 38 samples of 10 l of water taken from each of the water treatment steps and in 8 samples taken at home (only for Toxoplasma PCR) in Quindio region in Colombia. There were 8 positive samples for Cryptosporidium parvum (21 %), 4 for Cryptosporidium hominis (10.5 %), 27 for Toxoplasma gondii (58.6 %), 2 for Giardia duodenalis assemblage A (5.2 %), and 5 for G. duodenalis assemblage B (13.1 %). By IFAT, 23 % were positive for Giardia and 21 % for Cryptosporidium. An almost perfect agreement was found between IFAT and combined results of PCR, by Kappa composite proportion analysis. PCR positive samples were significantly more frequent in untreated raw water for C. parvum (p = 0.02). High mean of fecal coliforms, high pH values, and low mean of chlorine residuals were strongly correlated with PCR positivity for G. duodenalis assemblage B. High pH value was correlated with PCR positivity for C. parvum. Phylogenetic analysis of DNA sequences was possible, showing water and human clinical sequences for Toxoplasma within the same phylogenetic group for B1 repeated sequence. PCR assay is complementary to IFAT assay for monitoring of protozoa in raw and drinkable water, enabling species identification and to look for phylogenetic analysis in protozoa from human and environmental sources.

  15. Removal of impurities from environmental water samples for tritium measurement by means of liquid scintillation counter

    International Nuclear Information System (INIS)

    Sakuma, Yoichi; Noda, Mitsuyasu

    2000-01-01

    Tritium concentration in environmental water samples is usually measured by means of liquid scintillation counting. Before the counting distillation operation is necessarily required to remove impurities, which have possibility of bad influence on the measurement, from the samples. But the operation usually takes long time and it is also troublesome. If you could simplify the purification process, you would be much easily able to measure it. Then, we have studied the probability of replacement the process by filtration aiming to simplify the procedure. We prepared several environmental water samples and also several water samples added quenching materials. These samples were purified by means of the distillation and the filtration and the impurities in them were examined. The purified samples were mixed with scintillation cocktail and the tritium concentration was measured. We added small amount of tritium in the same samples and investigated their scintillation spectra and their ESCR values in order to compare the two purification methods. Two kinds of filters were used for the filtration: 0.45 μm and 0.1 μm pore sized membrane filters. The liquid scintillation counter was LB-3 produced by Aloka Co. and Ltd. The scintillation cocktail was Ultima Gold LLT made by Packard Instrument Co and Ltd. The vial was Polyvial 145 LSD made by Zinsser Analytic Co. and Ltd. As the result, there was no significant difference between the two purification methods then the filtration method is feasible instead of the distillation. (author)

  16. Identifying potential surface water sampling sites for emerging chemical pollutants in Gauteng Province, South Africa

    OpenAIRE

    Petersen, F; Dabrowski, JM; Forbes, PBC

    2017-01-01

    Emerging chemical pollutants (ECPs) are defined as new chemicals which do not have a regulatory status, but which may have an adverse effect on human health and the environment. The occurrence and concentrations of ECPs in South African water bodies are largely unknown, so monitoring is required in order to determine the potential threat that these ECPs may pose. Relevant surface water sampling sites in the Gauteng Province of South Africa were identified utilising a geographic information sy...

  17. Assessment of Heavy Metals in Water Samples of Certain Locations Situated Around Tumkur, Karnataka, India

    Directory of Open Access Journals (Sweden)

    C. Vijaya Bhaskar

    2010-01-01

    Full Text Available Surface water and groundwater samples of certain locations namely Kallambella, Bugudanahalli, Maidala, Honnudike, Kunigal, Kadaba and Hebbur, situated around Tumkur were assessed in the month of September 2008 for pH, EC and heavy metals Cd, Cu, Fe, Hg, Mn, Zn and Ni. The pH vales of surface waters were in alkaline range of 7.8-8.2 and are well within safe limits for crop production. The pH of ground- water was in the range of 7.6-8.4. The conductivity was in the range of 0.20-0.68 mS/cm and 0.34-2.44 mS/cm for surface and groundwaters respectively. High EC value of Kallambella groundwater accounts for its salinity. All surface waters except Honnudike and Hebbur samples contain low concentrations of these metals and are ideal for irrigation. Though the samples from Honnudike, Kadaba and Hebbur have high iron concentration, only Honnudike and Hebbur samples have exceeded the limit of 5 mg/L required for irrigation. In groundwaters the concentrations of all these heavy metals except copper are also well in permissible limits and suitable for drinking. Cu, Fe, Ni and Zn were detected in all the samples and found in the range of 0.094-0.131, 0.958-12.537, 0.020-0.036 and 0.082-1.139 mg/L respectively in surface waters and these are in the range of 0.132-0.142, 0.125-1.014, 0.028-0.036 and 0.003-0.037 mg/L in ground- waters. The elements cadmium, mercury and manganese are absent in all the samples.

  18. Precipitation and ion floatation of molybdenum, tungsten, copper, and cobalt compounds by cetyltrimethylammonium bromide and sodium diethyldithiocarbamate

    International Nuclear Information System (INIS)

    Strizhko, V.S.; Shekhirev, D.V.; Ignatkina, V.A.; Alimova, R.Eh.

    1996-01-01

    Experimental data are presented on application of ion-flotation in purification of low-concentration (less than 10 -3 M) acid solutions from molybdenum, tungsten, copper and cobalt ions. Two collectors, i.e. DEDC and CTMAB have been tested, their optimal consumption is determined. It is shown that CTMAB provides for selective purification from Mo and W ions and allows foam product with little water on flotation in a column to be obtained. But the achieved residual W and Mo concentration of 20 to 10 mg/l require deeper finishing purification in order to meet a sanitary permissible limiting concentration value employing other methods. DEDC provides for sufficient purification from nonferrous metal ions but does not possess selectivity with respect to some metals. The obtained results have shown the possibility to apply ion-flotation in concentration of metal ions in foam product in the process of waste water purification with further finishing purification up to a sanitary permissible limiting concentration value. 14 refs.; 3 figs.; 1 tab

  19. Development of a protocol for sampling and analysis of ballast water in Jamaica

    Directory of Open Access Journals (Sweden)

    Achsah A Mitchell

    2014-09-01

    Full Text Available The transfer of ballast by the international shipping industry has negatively impacted the environment. To design such a protocol for the area, the ballast water tanks of seven bulk cargo vessels entering a Jamaican port were sampled between January 28, 2010 and August 17, 2010. Vessels originated from five ports and used three main routes, some of which conducted ballast water exchange. Twenty-six preserved and 22 live replicate zooplankton samples were obtained. Abundance and richness were higher than at temperate ports. Exchange did not alter the biotic composition but reduced the abundance. Two of the live sample replicates, containing 31.67 and 16.75 viable individuals m-3, were non-compliant with the International Convention for the Control and Management of Ships’ Ballast Water and Sediments. Approximately 12% of the species identified in the ballast water were present in the waters nearest the port in 1995 and 11% were present in the entire bay in 2005. The protocol designed from this study can be used to aid the establishment of a ballast water management system in the Caribbean or used as a foundation for the development of further protocols.

  20. Field sampling of soil pore water to evaluate trace element mobility and associated environmental risk

    Energy Technology Data Exchange (ETDEWEB)

    Moreno-Jimenez, Eduardo, E-mail: eduardo.moreno@uam.es [Departamento de Quimica Agricola, Universidad Autonoma de Madrid, 28049 Madrid (Spain); Beesley, Luke [James Hutton Institute, Craigiebuckler, Aberdeen AB15 8QH (United Kingdom); Lepp, Nicholas W. [35, Victoria Road, Formby, Liverpool L37 7DH (United Kingdom); Dickinson, Nicholas M. [Department of Ecology, Lincoln University, Lincoln 7647, PO Box 84 (New Zealand); Hartley, William [School of Computing, Science and Engineering, University of Salford, Cockcroft Building, Salford, M5 4WT (United Kingdom); Clemente, Rafael [Dep. of Soil and Water Conservation and Organic Waste Management, CEBAS-CSIC, Campus Universitario de Espinardo, PO Box 164, 30100 Espinardo, Murcia (Spain)

    2011-10-15

    Monitoring soil pollution is a key aspect in sustainable management of contaminated land but there is often debate over what should be monitored to assess ecological risk. Soil pore water, containing the most labile pollutant fraction in soils, can be easily collected in situ offering a routine way to monitor this risk. We present a compilation of data on concentration of trace elements (As, Cd, Cu, Pb, and Zn) in soil pore water collected in field conditions from a range of polluted and non-polluted soils in Spain and the UK during single and repeated monitoring, and propose a simple eco-toxicity test using this media. Sufficient pore water could be extracted for analysis both under semi-arid and temperate conditions, and eco-toxicity comparisons could be effectively made between polluted and non-polluted soils. We propose that in-situ pore water extraction could enhance the realism of risk assessment at some contaminated sites. - Highlights: > In situ pore water sampling successfully evaluates trace elements mobility in soils. > Field sampling proved robust for different soils, sites and climatic regimes. > Measurements may be directly related to ecotoxicological assays. > Both short and long-term monitoring of polluted lands may be achieved. > This method complements other widely used assays for environmental risk assessment. - In situ pore water sampling from a wide variety of soils proves to be a beneficial application to monitor the stability of pollutants in soils and subsequent risk through mobility.

  1. Glufosinate ammonium clean-up procedure from water samples using SPE

    Science.gov (United States)

    Tayeb M., A.; Ismail B., S.; Mardiana-Jansar, K.; Ta, Goh Choo; Agustar, Hani Kartini

    2015-09-01

    For the determination of glufosinate ammonium residue in soil and water samples, different solid phase extraction (SPE) sorbent efficiency was studied. Four different SPE sorbents i.e.: CROMABOND PS-H+, CROMABOND PS-OH-, ISOLUTE ENV+, Water Sep-Pak and OASIS HLB were used. Sample clean-up performance was evaluated using high performance liquid chromatography (Agilent 1220 infinity LC) with fluorescence detector. Detection of FMO-derivatives was done at λ ex = 260 nm and λ em= 310 nm. OASIS HLB column was the most suitable for the clean-up in view of the overall feasibility of the analysis.

  2. Adsorptive stripping voltammetric determination of trace amounts of lead in environmental water samples with complicated matrix

    Directory of Open Access Journals (Sweden)

    Grabarczyk M.

    2013-04-01

    Full Text Available A sensitive, simple and fast adsorptive stripping voltammetric procedure for trace determination of lead in environmental water samples has been developed. The method is based on adsorptive accumulation of the Pb(II-cupferron complex onto a hanging mercury drop electrode, followed by the reduction of the adsorbed species by a voltammetric scan using differential pulse modulation. The interference from surface active substances was eliminated by adsorption of interferents onto an Amberlite XAD-16 resin. Optimumconditions for removing the surfactants by mixing the analysed sample with resin were evaluated. The accuracy of the method was tested by analyzing certified reference material (SPS-WW1 Waste Water.

  3. Classification and authentication of unknown water samples using machine learning algorithms.

    Science.gov (United States)

    Kundu, Palash K; Panchariya, P C; Kundu, Madhusree

    2011-07-01

    This paper proposes the development of water sample classification and authentication, in real life which is based on machine learning algorithms. The proposed techniques used experimental measurements from a pulse voltametry method which is based on an electronic tongue (E-tongue) instrumentation system with silver and platinum electrodes. E-tongue include arrays of solid state ion sensors, transducers even of different types, data collectors and data analysis tools, all oriented to the classification of liquid samples and authentication of unknown liquid samples. The time series signal and the corresponding raw data represent the measurement from a multi-sensor system. The E-tongue system, implemented in a laboratory environment for 6 numbers of different ISI (Bureau of Indian standard) certified water samples (Aquafina, Bisleri, Kingfisher, Oasis, Dolphin, and McDowell) was the data source for developing two types of machine learning algorithms like classification and regression. A water data set consisting of 6 numbers of sample classes containing 4402 numbers of features were considered. A PCA (principal component analysis) based classification and authentication tool was developed in this study as the machine learning component of the E-tongue system. A proposed partial least squares (PLS) based classifier, which was dedicated as well; to authenticate a specific category of water sample evolved out as an integral part of the E-tongue instrumentation system. The developed PCA and PLS based E-tongue system emancipated an overall encouraging authentication percentage accuracy with their excellent performances for the aforesaid categories of water samples. Copyright © 2011 ISA. Published by Elsevier Ltd. All rights reserved.

  4. The Alaska Commercial Fisheries Water Quality Sampling Methods and Procedures Manual

    Energy Technology Data Exchange (ETDEWEB)

    Folley, G.; Pearson, L.; Crosby, C. [Alaska Dept. of Environmental Conservation, Soldotna, AK (United States); DeCola, E.; Robertson, T. [Nuka Research and Planning Group, Seldovia, AK (United States)

    2006-07-01

    A comprehensive water quality sampling program was conducted in response to the oil spill that occurred when the M/V Selendang Ayu ship ran aground near a major fishing port at Unalaska Island, Alaska in December 2004. In particular, the sampling program focused on the threat of spilled oil to the local commercial fisheries resources. Spill scientists were unable to confidently model the movement of oil away from the wreck because of limited oceanographic data. In order to determine which fish species were at risk of oil contamination, a real-time assessment of how and where the oil was moving was needed, because the wreck became a continual source of oil release for several weeks after the initial grounding. The newly developed methods and procedures used to detect whole oil during the sampling program will be presented in the Alaska Commercial Fisheries Water Quality Sampling Methods and Procedures Manual which is currently under development. The purpose of the manual is to provide instructions to spill managers while they try to determine where spilled oil has or has not been encountered. The manual will include a meaningful data set that can be analyzed in real time to assess oil movement and concentration. Sections on oil properties and processes will be included along with scientific water quality sampling methods for whole and dissolved phase oil to assess potential contamination of commercial fishery resources and gear in Alaska waters during an oil spill. The manual will present a general discussion of factors that should be considered when designing a sampling program after a spill. In order to implement Alaska's improved seafood safety measures, the spatial scope of spilled oil must be known. A water quality sampling program can provide state and federal fishery managers and food safety inspectors with important information as they identify at-risk fisheries. 11 refs., 7 figs.

  5. Impact of recharge through residual oil upon sampling of underlying ground water

    International Nuclear Information System (INIS)

    Wise, W.R.; Chang, Chichung; Klopp, R.A.; Bedient, P.B.

    1991-01-01

    At an aviation gasoline spill site in Traverse City, Michigan, historical records indicate a positive correlation between significant rainfall events and increased concentrations of slightly soluble organic compounds in the monitoring wells of the site. To investigate the recharge effect on ground water quality due to infiltrating water percolating past residual oil and into the saturated zone, an in situ infiltration experiment was performed at the site. Sampling cones were set at various depths below a circular test area, 13 feet (4 meters) in diameter. Rainfall was simulated by sprinkling the test area at a rate sufficiently low to prevent runoff. The sampling cones for soil-gas and ground water quality were installed in the unsaturated and saturated zones to observed the effects of the recharge process. Infiltrated water was determined to have transported organic constituents of the residual oil, specifically benzene, toluene, ethylbenzene, and ortho-xylene (BTEX), into the ground water beneath the water table, elevating the aqueous concentrations of these constituents in the saturated zone. Soil-gas concentrations of the organic compounds in the unsaturated zone increased with depth and time after the commencement of infiltration. Reaeration of the unconfined aquifer via the infiltrated water was observed. It is concluded that water quality measurements are directly coupled to recharge events for the sandy type of aquifer with an overlying oil phase, which was studied in this work. Ground water sampling strategies and data analysis need to reflect the effect of recharge from precipitation on shallow, unconfined aquifers where an oil phase may be present

  6. A simplified method for low-level tritium measurement in the environmental water samples

    International Nuclear Information System (INIS)

    Sakuma, Yoichi; Yamanishi, Hirokuni; Ogata, Yoshimune

    2004-01-01

    Low level liquid scintillation counting took much time with a lot of doing to distill off the impurities in the sample water before mixing the sample with the liquid scintillation cocktail. In the light of it, we investigated the possibility of an alternative filtration method for sample purification. The tritium concentration in the environmental water has become very low, and the samples have to be treated by electrolysis enrichment with a liquid scintillation analyzer. Using the solid polymer electrolyte enriching device, there is no need to add neither any electrolyte nor the neutralization after the concentration. If we could replace the distillation process with the filtration, the procedure would be simplified very much. We investigated the procedure and we were able to prove that the reverse osmosis (RO) filtration was available. Moreover, in order to rationalize all through the measurement method, we examined the followings: (1) Improvement of the enriching apparatus. (2) Easier measurement of heavy water concentration using a density meter, instead of a mass spectrometer. The concentration of water samples was measured to determine the enrichment rate of tritium during the electrolysis enrichment. (author)

  7. Determination of different contaminants in selective drinking water samples collected from Peshawar valley area

    International Nuclear Information System (INIS)

    Ihsanullah; Khan, M.; Khattak, T.N.; Sattar, A.

    1999-01-01

    Among the pollutants carried through sewage, industrial effluents, fertilizers, pesticides; heavy metals and various pathogenic bacteria are directly related to human/animal diseases. Samples of drinking water were collected from different locations, in the Peshawar area. Cadmium, lead and copper levels in these samples were determined by potentiometric stripping analysis (PSA). The data indicated wide variation in the concentration of these heavy metals. Variation in results is discussed on the basis of some possible sources of contamination. The concentration of cadmium and lead in all the samples was higher compared to the values given in the guideline of World Health Organization (WHO) for drinking water. Copper was below the detection limit in majority of the samples. The values of Cd, Pb and Cu were in the range of 0.023-2.75, 0.025-1.88 and 0-0.67 mg/1 respectively. Various physical quality indices (ph, electrical conductivity and total solids) and pathogenic bacteria (E. coli and total coliforms) were also determined in water samples. Most of the drinking waters was found contaminated with higher levels of Cd and Pb and pathogenic bacteria and hence, considered unfit for drinking purposes. (author)

  8. UMTRA project water sampling and analysis plan, Falls City, Texas. Revision 1

    International Nuclear Information System (INIS)

    1995-09-01

    Planned, routine ground water sampling activities at the US Department of Energy (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project site near Falls City, Texas, are described in this water sampling and analysis plan (WSAP). The following plan identifies and justifies the sampling locations, analytical parameters, and sampling frequency for the routine monitoring stations at the site. The ground water data are used for site characterization and risk assessment. The regulatory basis for routine ground water monitoring at UMTRA Project sites is derived from the US Environmental Protection Agency (EPA) regulations in 40 CFR Part 192. Sampling procedures are guided by the UMTRA Project standard operating procedures (SOP) (JEG, n.d.), the Technical Approach Document (TAD) (DOE, 1989), and the most effective technical approach for the site. The Falls City site is in Karnes County, Texas, approximately 8 miles [13 kilometers southwest of the town of Falls City and 46 mi (74 km) southeast of San Antonio, Texas. Before surface remedial action, the tailings site consisted of two parcels. Parcel A consisted of the mill site, one mill building, five tailings piles, and one tailings pond south of Farm-to-Market (FM) Road 1344 and west of FM 791. A sixth tailings pile designated Parcel B was north of FM 791 and east of FM 1344

  9. Adaptive Kalman Filter Based on Adjustable Sampling Interval in Burst Detection for Water Distribution System

    Directory of Open Access Journals (Sweden)

    Doo Yong Choi

    2016-04-01

    Full Text Available Rapid detection of bursts and leaks in water distribution systems (WDSs can reduce the social and economic costs incurred through direct loss of water into the ground, additional energy demand for water supply, and service interruptions. Many real-time burst detection models have been developed in accordance with the use of supervisory control and data acquisition (SCADA systems and the establishment of district meter areas (DMAs. Nonetheless, no consideration has been given to how frequently a flow meter measures and transmits data for predicting breaks and leaks in pipes. This paper analyzes the effect of sampling interval when an adaptive Kalman filter is used for detecting bursts in a WDS. A new sampling algorithm is presented that adjusts the sampling interval depending on the normalized residuals of flow after filtering. The proposed algorithm is applied to a virtual sinusoidal flow curve and real DMA flow data obtained from Jeongeup city in South Korea. The simulation results prove that the self-adjusting algorithm for determining the sampling interval is efficient and maintains reasonable accuracy in burst detection. The proposed sampling method has a significant potential for water utilities to build and operate real-time DMA monitoring systems combined with smart customer metering systems.

  10. Umbrella sampling of proton transfer in a creatine-water system

    Science.gov (United States)

    Ivchenko, Olga; Bachert, Peter; Imhof, Petra

    2014-04-01

    Proton transfer reactions are among the most common processes in chemistry and biology. Proton transfer between creatine and surrounding solvent water is underlying the chemical exchange saturation transfer used as a contrast in magnetic resonance imaging. The free energy barrier, determined by first-principles umbrella sampling simulations (EaDFT 3 kcal/mol) is in the same order of magnitude as the experimentally obtained activation energy. The underlying mechanism is a first proton transfer from the guanidinium group to the water pool, followed by a second transition where a proton is "transferred back" from the nearest water molecule to the deprotonated nitrogen atom of creatine.

  11. Frequency of hepatitis E and Hepatitis A virus in water sample collected from Faisalabad, Pakistan

    Directory of Open Access Journals (Sweden)

    Tahir Ahmad

    2015-12-01

    Full Text Available Hepatitis E and Hepatitis A virus both are highly prevalent in Pakistan mainly present as a sporadic disease. The aim of the current study is to isolate and characterized the specific genotype of Hepatitis E virus from water bodies of Faisalabad, Pakistan. Drinking and sewage samples were qualitatively analyzed by using RT-PCR. HEV Genotype 1 strain was recovered from sewage water of Faisalabad. Prevalence of HEV and HAV in sewage water propose the possibility of gradual decline in the protection level of the circulated vaccine in the Pakistani population.

  12. Removal of arsenic from ground water samples collected from West Bengal, India

    International Nuclear Information System (INIS)

    Ajith, Nicy; Swain, K.K.; Dalvi, Aditi A.; Verma, R.

    2015-01-01

    Arsenic contamination in ground water is one of the major concerns in many parts of the world including Bangladesh and India. Considering the high toxicity of arsenic, World Health Organization (WHO) has set a provisional guideline value of 10 μg L -1 for arsenic in drinking water. Several methods have been adopted for the removal of arsenic from drinking water. Most of the methods fail to remove As(III), the most toxic form of arsenic. An extra oxidative treatment step is essential for effective removal of total arsenic. Manganese dioxide (MnO 2 ) oxidizes As(III) to As(V). Removal of arsenic from water using manganese dioxide has been reported. During this work, removal of arsenic from ground water samples collected from arsenic contaminated area of West Bengal, India were carried out using MnO 2

  13. Determination of anionic concentrations in ground water samples using ion chromatography

    International Nuclear Information System (INIS)

    Prathibha, P.; Saradhi, I.V.; Pandit, G.G.; Puranik, V.D.

    2011-01-01

    Ion chromatography is a powerful separation technique for the quantitative measurement of anions in aqueous samples as well as in soil, sediment and air particulate samples leached in aqueous solutions. Ion chromatographic technique is developed by making use of suppressed ion conductivity detection (Small et.al.,1975) and it is a rapid multi ion analysis technique. The time, processing and effort required for the analysis of anions is much less compared to other techniques available such as ion selective electrode technique. In the present paper ground water samples collected around New BARC campus, Visakhapatnam are analyzed for anions using Ion chromatograph. The data generated will establish the current baseline status of the ionic contaminants in the study area. Groundwater samples are collected at 13 locations around BARC Vizag campus covering 30 km radius in September, 2009, April and July, 2010. The water samples include samples from hand pump and open wells in villages. The water samples are analyzed for fluoride, chloride, nitrate and sulphate using Metrohm make Ion chromatograph. The fluoride concentration in samples varied from 0.22 to 1.26 ppm, chloride from 18.7 to 810.9, nitrate from 1.34 to 378.5 ppm and sulphate from 13.29 to 250.69 ppm. No significant seasonal variations are observed in the samples collected from various locations except chloride at two locations. Ions Chromatograph is found to be a useful tool for simultaneous analysis of environmental samples with good accuracy where the concentrations of anions vary within an order of magnitude among them themselves. (author)

  14. Infrared thermometry and the crop water stress index. II. Sampling procedures and interpretation

    Energy Technology Data Exchange (ETDEWEB)

    Gardner, B. R. [BP Research, Cleveland, OH (United States); Nielsen, D. C.; Shock, C. C.

    1992-10-15

    Infrared thermometry can be a valuable research and production tool for detecting and quantifying water stress in plants, as shown by a large volume of published research. Users of infrared thermometers (IRT) should be aware of the many equipment, environmental, and plant factors influencing canopy temperature measured by an IRT. The purpose of this paper is to describe factors influencing measured plant temperature, outline sampling procedures that will produce reliable Crop Water Stress Index (CWSI) values, and offer interpretations of CWSI and plant temperatures relative to crop production and other water stress parameters by reviewing previously conducted research. Factors that are considered are IRT condition, configuration, and position; psychrometer location; wind speed; solar radiation; time of day; leaf area and orientation; and appropriate non-water-stressed baseline equation. Standard sampling and CWSI calculation procedures are proposed. Use of CWSI with crops varying in type of response to water stress is described. Previously conducted research on plant temperatures or CWSI is tabulated by crop and water stress parameters measured. The paper provides valuable information to assist interested users of IRTs in making reliable water stress measurements. (author)

  15. Infrared thermometry and the crop water stress index. II. Sampling procedures and interpretation

    International Nuclear Information System (INIS)

    Gardner, B.R.; Nielsen, D.C.; Shock, C.C.

    1992-01-01

    Infrared thermometry can be a valuable research and production tool for detecting and quantifying water stress in plants, as shown by a large volume of published research. Users of infrared thermometers (IRT) should be aware of the many equipment, environmental, and plant factors influencing canopy temperature measured by an IRT. The purpose of this paper is to describe factors influencing measured plant temperature, outline sampling procedures that will produce reliable Crop Water Stress Index (CWSI) values, and offer interpretations of CWSI and plant temperatures relative to crop production and other water stress parameters by reviewing previously conducted research. Factors that are considered are IRT condition, configuration, and position; psychrometer location; wind speed; solar radiation; time of day; leaf area and orientation; and appropriate non-water-stressed baseline equation. Standard sampling and CWSI calculation procedures are proposed. Use of CWSI with crops varying in type of response to water stress is described. Previously conducted research on plant temperatures or CWSI is tabulated by crop and water stress parameters measured. The paper provides valuable information to assist interested users of IRTs in making reliable water stress measurements. (author)

  16. Metal quantification in water and sediment samples of billings reservoir by SR-TXRF

    International Nuclear Information System (INIS)

    Sampaio, Sergio Arnaud; Moreira, Silvana; Vives, Ana Elisa Sirito de

    2007-01-01

    Billings is the largest reservoir water of the metropolitan Sao Paulo area, with approximately 100km 2 of water. Its basin hydrographic occupies more than 500km 2 in six cities. It concentrates the largest industrial park of South America and only its margins are busy for almost a million inhabitants. The quality of its waters is, therefore, constant of concern of the whole society. In this work the Synchrotron Radiation Total Reflection X Ray Fluorescence (SR-TXRF) is applied for the identification and quantification of metals in waters and sediments of the Billings dam. A comparison of the levels of metals found with the maximum permissive limits established by the Brazilian legislation was made. The purpose of social context is to contribute for the preservation of the local springs and the rational use of its waters. For the field work they were chosen 19 collection points, included the margins and the central portion of the dam, in agreement with similar approaches the those adopted by the Company of Technology of Environmental Sanitation of Sao Paulo State (CETESB).The water and sediment samples, as well as the certified and standard samples, were analyzed at Brazilian Synchrotron Light Laboratory (LNLS), Campinas, SP, Brazil. Results indicate that the water and the sediments of the reservoir have concentrations above the legal limits. (author)

  17. Metal quantification in water and sediment samples of billings reservoir by SR-TXRF

    Energy Technology Data Exchange (ETDEWEB)

    Sampaio, Sergio Arnaud; Moreira, Silvana [Universidade Estadual de Campinas (UNICAMP), Campinas, SP (Brazil). Faculdade de Engenharia Civil, Arquitetura e Urbanismo]. E-mails: silvana@fec.unicamp.br; sergioarnaud@hotmail.com; Vives, Ana Elisa Sirito de [Universidade Metodista de Piracicaba (UNIMEP), Santa Barbara D' Oeste, SP (Brazil). Faculdade de Engenharia Civil, Arquitetura e Urbanismo]. E-mail: aesvives@unimep.br

    2007-07-01

    Billings is the largest reservoir water of the metropolitan Sao Paulo area, with approximately 100km{sup 2} of water. Its basin hydrographic occupies more than 500km{sup 2} in six cities. It concentrates the largest industrial park of South America and only its margins are busy for almost a million inhabitants. The quality of its waters is, therefore, constant of concern of the whole society. In this work the Synchrotron Radiation Total Reflection X Ray Fluorescence (SR-TXRF) is applied for the identification and quantification of metals in waters and sediments of the Billings dam. A comparison of the levels of metals found with the maximum permissive limits established by the Brazilian legislation was made. The purpose of social context is to contribute for the preservation of the local springs and the rational use of its waters. For the field work they were chosen 19 collection points, included the margins and the central portion of the dam, in agreement with similar approaches the those adopted by the Company of Technology of Environmental Sanitation of Sao Paulo State (CETESB).The water and sediment samples, as well as the certified and standard samples, were analyzed at Brazilian Synchrotron Light Laboratory (LNLS), Campinas, SP, Brazil. Results indicate that the water and the sediments of the reservoir have concentrations above the legal limits. (author)

  18. Simple Modification of Karl-Fischer Titration Method for Determination of Water Content in Colored Samples

    OpenAIRE

    Eva Tavčar; Erika Turk; Samo Kreft

    2012-01-01

    The most commonly used technique for water content determination is Karl-Fischer titration with electrometric detection, requiring specialized equipment. When appropriate equipment is not available, the method can be performed through visual detection of a titration endpoint, which does not enable an analysis of colored samples. Here, we developed a method with spectrophotometric detection of a titration endpoint, appropriate for moisture determination of colored samples. The reaction takes p...

  19. Program for TI programmable 59 calculator for calculation of 3H concentration of water samples

    International Nuclear Information System (INIS)

    Hussain, S.D.; Asghar, G.

    1982-09-01

    A program has been developed for TI Programmable 59 Calculator of Texas Instruments Inc. to calculate from the observed parameters such as count rate etc. the 3 H (tritium) concentration of water samples processed with/without prior electrolytic enrichment. Procedure to use the program has been described in detail. A brief description of the laboratory treatment of samples and the mathematical equations used in the calculations have been given. (orig./A.B.)

  20. Demonstration/Validation of the Snap Sampler Passive Ground Water Sampling Device

    Science.gov (United States)

    2011-06-01

    purging and sampling protocol. Analytes that were measured at the Pease site included total and dissolved concentrations of arsenic (As), calcium ...samples remain in the original bottle in which they were collected, presumably losses of volatiles and changes in concentrations of dissolved gases or...because of excavation and removal. This has resulted in hydraulically interconnected bedrock and overburden water- bearing zones in much of this area

  1. {sup 222}Rn determination in water and brine samples using liquid scintillation spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Thiago C.; Oliveira, Arno H., E-mail: oliveiratco2010@gmail.com [Universidade Federal de Minas Gerais (DEN/UFMG), Belo Horizonte (Brazil). Departamento de Engenharia Nuclear; Monteiro, Roberto P.G.; Moreira, Rubens M., E-mail: rpgm@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN-CNEN-MG), Belo Horizonte, MG (Brazil)

    2017-07-01

    Liquid scintillation spectrometry (LSC) is the most common technique used for {sup 222}Rn determination in environmental aqueous sample. In this study, the performance of water-miscible (Ultima Gold AB) and immiscible (Optiscint) liquid scintillation cocktails has been compared for different matrices. {sup 241}Am, {sup 90}Sr and {sup 226}Ra standard solutions were used for LSC calibration. {sup 214}Po region was defined as better for both cocktails. Counting efficiency of 76 % and optimum PSA level of 95 for Ultima Gold AB cocktail, and counting efficiency of 82 % and optimum PSA level of 85 for Optiscint cocktail were obtained. Both cocktails showed similar results when applied for {sup 222}Rn activity determination in water and brine samples. However the Optiscint is recommended due to its quenching resistance. Limit of detection of 0.08 and 0.06 Bq l{sup -1} were obtained for water samples using a sample:cocktail ratio of 10:12 mL for Ultima Gold AB and Optiscint cocktails, respectively. Limit of detection of 0.08 and 0.04 Bq l{sup -1} were obtained for brine samples using a sample:cocktail ratio of 8:12 mL for Ultima Gold AB and Optiscint cocktails, respectively. (author)

  2. 222Rn determination in water and brine samples using liquid scintillation spectrometry

    International Nuclear Information System (INIS)

    Oliveira, Thiago C.; Oliveira, Arno H.

    2017-01-01

    Liquid scintillation spectrometry (LSC) is the most common technique used for 222 Rn determination in environmental aqueous sample. In this study, the performance of water-miscible (Ultima Gold AB) and immiscible (Optiscint) liquid scintillation cocktails has been compared for different matrices. 241 Am, 90 Sr and 226 Ra standard solutions were used for LSC calibration. 214 Po region was defined as better for both cocktails. Counting efficiency of 76 % and optimum PSA level of 95 for Ultima Gold AB cocktail, and counting efficiency of 82 % and optimum PSA level of 85 for Optiscint cocktail were obtained. Both cocktails showed similar results when applied for 222 Rn activity determination in water and brine samples. However the Optiscint is recommended due to its quenching resistance. Limit of detection of 0.08 and 0.06 Bq l -1 were obtained for water samples using a sample:cocktail ratio of 10:12 mL for Ultima Gold AB and Optiscint cocktails, respectively. Limit of detection of 0.08 and 0.04 Bq l -1 were obtained for brine samples using a sample:cocktail ratio of 8:12 mL for Ultima Gold AB and Optiscint cocktails, respectively. (author)

  3. The installation of a multiport ground-water sampling system in the 300 Area

    International Nuclear Information System (INIS)

    Gilmore, T.J.

    1989-06-01

    In 1988, the Pacific Northwest Laboratory installed a multiport groundwater sampling system in well 399-1-20, drilled north of the 300 Area on the Hanford Site in southwestern Washington State. The purpose of installing the multiport system is to evaluate methods of determining the vertical distribution of contaminants and hydraulic heads in ground water. Well 399-1-20 is adjacent to a cluster of four Resource Conservation and Recovery Act (RCRA) ground-water monitoring wells. This proximity makes it possible to compare sampling intervals and head measurements between the multiport system and the RCRA monitoring wells. Drilling and installation of the multiport system took 42 working days. Six sampling ports were installed in the upper unconfined aquifer at depths of approximately 120, 103, 86, 74, 56, and 44 feet. The locations of the sampling ports were determined by the hydrogeology of the area and the screened intervals of adjacent ground-water monitoring wells. The system was installed by backfilling sand around the sampling ports and isolating the ports with bentonite seals. The method proved adequate. For future installation, however, development and evaluation of an alternative method is recommended. In the alternative method suggested, the multiport system would be placed inside a cased and screened well, using packers to isolate the sampling zones. 4 refs., 8 figs., 1 tab

  4. Method validation to determine total alpha beta emitters in water samples using LSC

    International Nuclear Information System (INIS)

    Al-Masri, M. S.; Nashawati, A.; Al-akel, B.; Saaid, S.

    2006-06-01

    In this work a method was validated to determine gross alpha and beta emitters in water samples using liquid scintillation counter. 200 ml of water from each sample were evaporated to 20 ml and 8 ml of them were mixed with 12 ml of the suitable cocktail to be measured by liquid scintillation counter Wallac Winspectral 1414. The lower detection limit by this method (LDL) was 0.33 DPM for total alpha emitters and 1.3 DPM for total beta emitters. and the reproducibility limit was (± 2.32 DPM) and (±1.41 DPM) for total alpha and beta emitters respectively, and the repeatability limit was (±2.19 DPM) and (±1.11 DPM) for total alpha and beta emitters respectively. The method is easy and fast because of the simple preparation steps and the large number of samples that can be measured at the same time. In addition, many real samples and standard samples were analyzed by the method and showed accurate results so it was concluded that the method can be used with various water samples. (author)

  5. External quality control in ground-water sampling and analysis at the Hanford Site

    International Nuclear Information System (INIS)

    Hall, S.H.; Juracich, S.P.

    1991-11-01

    At the US Department of Energy's Hanford Site, external Quality Control (QC) for ground-water monitoring is extensive and has included routine submittal of intra- and interlaboratory duplicate samples, blind samples, and several kinds of blank samples. Examination of the resulting QC data for nine of the constituents found in ground water at the Hanford Site shows that the quality of analysis has generally been within the expectations of precision and accuracy that have been established by the US Environmental Protection Agency (EPA). The constituents subjected to review were nitrate, chromium, sodium, fluoride, carbon tetrachloride, tritium, ammonium, trichloroethylene, and cyanide. Of these, the fluoride measurements were notable exceptions and were poor by EPA standards. The review has shown that interlaboratory analysis of duplicate samples yields the most useful QC data for evaluating laboratory performance in determining commonly encountered constituents. For rarely encountered constituents, interlaboratory comparisons may be augmented with blind samples (synthetic samples of known composition). Intralaboratory comparisons, blanks, and spikes should be generally restricted to studies of suspected or known sample contamination and to studies of the adequacy of sampling and analytical procedures

  6. Physiological response of wild dugongs (Dugong dugon) to out-of-water sampling for health assessment

    Science.gov (United States)

    Lanyon, Janet M.; Sneath, Helen L.; Long, Trevor; Bonde, Robert K.

    2010-01-01

    The dugong (Dugong dugon) is a vulnerable marine mammal with large populations living in urban Queensland waters. A mark-recapture program for wild dugongs has been ongoing in southern Queensland since 2001. This program has involved capture and in-water sampling of more than 700 dugongs where animals have been held at the water surface for 5 min to be gene-tagged, measured, and biopsied. In 2008, this program expanded to examine more comprehensively body condition, reproductive status, and the health of wild dugongs in Moreton Bay. Using Sea World's research vessel, captured dugongs were lifted onto a boat and sampled out-of-water to obtain accurate body weights and morphometrics, collect blood and urine samples for baseline health parameters and hormone profiles, and ultrasound females for pregnancy status. In all, 30 dugongs, including two pregnant females, were sampled over 10 d and restrained on deck for up to 55 min each while biological data were collected. Each of the dugongs had their basic temperature-heart rate-respiration (THR) monitored throughout their period of handling, following protocols developed for the West Indian manatee (Trichechus manatus). This paper reports on the physiological response of captured dugongs during this out-of-water operation as indicated by their vital signs and the suitability of the manatee monitoring protocols to this related sirenian species. A recommendation is made that the range of vital signs of these wild dugongs be used as benchmark criteria of normal parameters for other studies that intend to sample dugongs out-of-water.

  7. Robowell: An automated process for monitoring ground water quality using established sampling protocols

    Science.gov (United States)

    Granato, G.E.; Smith, K.P.

    1999-01-01

    Robowell is an automated process for monitoring selected ground water quality properties and constituents by pumping a well or multilevel sampler. Robowell was developed and tested to provide a cost-effective monitoring system that meets protocols expected for manual sampling. The process uses commercially available electronics, instrumentation, and hardware, so it can be configured to monitor ground water quality using the equipment, purge protocol, and monitoring well design most appropriate for the monitoring site and the contaminants of interest. A Robowell prototype was installed on a sewage treatment plant infiltration bed that overlies a well-studied unconfined sand and gravel aquifer at the Massachusetts Military Reservation, Cape Cod, Massachusetts, during a time when two distinct plumes of constituents were released. The prototype was operated from May 10 to November 13, 1996, and quality-assurance/quality-control measurements demonstrated that the data obtained by the automated method was equivalent to data obtained by manual sampling methods using the same sampling protocols. Water level, specific conductance, pH, water temperature, dissolved oxygen, and dissolved ammonium were monitored by the prototype as the wells were purged according to U.S Geological Survey (USGS) ground water sampling protocols. Remote access to the data record, via phone modem communications, indicated the arrival of each plume over a few days and the subsequent geochemical reactions over the following weeks. Real-time availability of the monitoring record provided the information needed to initiate manual sampling efforts in response to changes in measured ground water quality, which proved the method and characterized the screened portion of the plume in detail through time. The methods and the case study described are presented to document the process for future use.

  8. Screening and Quantification of Aliphatic Primary Alkyl Corrosion Inhibitor Amines in Water Samples by Paper Spray Mass Spectrometry.

    Science.gov (United States)

    Jjunju, Fred P M; Maher, Simon; Damon, Deidre E; Barrett, Richard M; Syed, S U; Heeren, Ron M A; Taylor, Stephen; Badu-Tawiah, Abraham K

    2016-01-19

    Direct analysis and identification of long chain aliphatic primary diamine Duomeen O (n-oleyl-1,3-diaminopropane), corrosion inhibitor in raw water samples taken from a large medium pressure water tube boiler plant water samples at low LODs (corrosion inhibitors in an industrial water boiler plant and other related samples in the water treatment industry. This approach was applied for the analysis of three complex water samples including feedwater, condensate water, and boiler water, all collected from large medium pressure (MP) water tube boiler plants, known to be dosed with varying amounts of polyamine and amine corrosion inhibitor components. Polyamine chemistry is widely used for example in large high pressure (HP) boilers operating in municipal waste and recycling facilities to prevent corrosion of metals. The samples used in this study are from such a facility in Coventry waste treatment facility, U.K., which has 3 × 40 tonne/hour boilers operating at 17.5 bar.

  9. Solvent-assisted dispersive solid-phase extraction: A sample preparation method for trace detection of diazinon in urine and environmental water samples.

    Science.gov (United States)

    Aladaghlo, Zolfaghar; Fakhari, Alireza; Behbahani, Mohammad

    2016-09-02

    In this research, a sample preparation method termed solvent-assisted dispersive solid-phase extraction (SA-DSPE) was applied. The used sample preparation method was based on the dispersion of the sorbent into the aqueous sample to maximize the interaction surface. In this approach, the dispersion of the sorbent at a very low milligram level was received by inserting a solution of the sorbent and disperser solvent into the aqueous sample. The cloudy solution created from the dispersion of the sorbent in the bulk aqueous sample. After pre-concentration of the diazinon, the cloudy solution was centrifuged and diazinon in the sediment phase dissolved in ethanol and determined by gas chromatography-flame ionization detector. Under the optimized conditions (pH of solution=7.0, Sorbent: benzophenone, 2%, Disperser solvent: ethanol, 500μL, Centrifuge: centrifuged at 4000rpm for 3min), the method detection limit for diazinon was 0.2, 0.3, 0.3 and 0.3μgL(-1) for distilled water, lake water, waste water and urine sample, respectively. Furthermore, the pre-concentration factor was 363.8, 356.1, 360.7 and 353.38 in distilled water, waste water, lake water and urine sample, respectively. SA-DSPE was successfully used for trace monitoring of diazinon in urine, lake and waste water samples. Copyright © 2016 Elsevier B.V. All rights reserved.

  10. Water Quality Sampling Locations Along the Shoreline of the Columbia River, Hanford Site, Washington

    Energy Technology Data Exchange (ETDEWEB)

    Peterson, Robert E.; Patton, Gregory W.

    2009-12-14

    As environmental monitoring evolved on the Hanford Site, several different conventions were used to name or describe location information for various sampling sites along the Hanford Reach of the Columbia River. These methods range from handwritten descriptions in field notebooks to the use of modern electronic surveying equipment, such as Global Positioning System receivers. These diverse methods resulted in inconsistent archiving of analytical results in various electronic databases and published reports because of multiple names being used for the same site and inaccurate position data. This document provides listings of sampling sites that are associated with groundwater and river water sampling. The report identifies names and locations for sites associated with sampling: (a) near-river groundwater using aquifer sampling tubes; (b) riverbank springs and springs areas; (c) pore water collected from riverbed sediment; and (d) Columbia River water. Included in the listings are historical names used for a particular site and the best available geographic coordinates for the site, as of 2009. In an effort to create more consistency in the descriptive names used for water quality sampling sites, a naming convention is proposed in this document. The convention assumes that a unique identifier is assigned to each site that is monitored and that this identifier serves electronic database management requirements. The descriptive name is assigned for the convenience of the subsequent data user. As the historical database is used more intensively, this document may be revised as a consequence of discovering potential errors and also because of a need to gain consensus on the proposed naming convention for some water quality monitoring sites.

  11. Membrane solid-phase extraction: Field application for isolation of polycyclic aromatic hydrocarbons from water samples

    International Nuclear Information System (INIS)

    Furlong, E.T.; Koleis, J.C.; Gates, P.M.

    1995-01-01

    Solid-phase extraction (SPE) membranes (M-SPE) were used to isolate microgram-per-liter to nanogram-per-liter quantities of polycyclic aromatic hydrocarbons (PAH) in 4- to 8-liter ground-water samples from a crude-oil-contaminated ground-water site near Bemidji, Minnesota. The M-SPE method was evaluated (1) under laboratory conditions using reagent water fortified with individual PAH at 1.23 micrograms per liter, and (2) at the Bemidji site. At the site, ground-water samples were processed and PAH isolated using a M-SPE system connected directly to the well pump. Following sample isolation, all M-SPE samples were extracted using dichloromethane and analyzed by gas chromatography-mass spectrometry with selected-ion monitoring. Operationally, the M-SPE method provided a simple means to isolate PAH on site at the wellhead, particularly for anoxic water samples. Acceptable recoveries, ranging from 56 to over 100 percent, were observed for lower molecular weight PAH (naphthalene to pyrene) using the M-SPE method. Recoveries using M-SPE were somewhat lower, but reproducible, for higher molecular weight PAH (chrysene to benzo[ghi]perylene), ranging from 18 to 56 percent. M-SPE provides the capability to collect and field isolate PAH from a sufficiently large number of samples to identify environmental chemical processes occurring at individual compound concentrations of 50 to 1,200 nanograms per liter. Using M-SPE, the potential for facilitated transport of PAH by in situ-derived dissolved organic carbon (DOC) was evaluated at the site. Plots comparing DOC and PAH concentrations indicate that PAH concentrations increase exponentially with linear increases in DOC concentrations

  12. Determination of radon and radium concentrations in drinking water samples around the city of Kutahya

    International Nuclear Information System (INIS)

    Sahin, L.; Cetinkaya, H.; Murat Sac, M.; Ichedef, M.

    2013-01-01

    The concentration of radium and radon has been determined in drinking water samples collected from various locations of Kutahya city, Turkey. The water samples are taken from public water sources and tap water, with the collector chamber method used to measure the radon and radium concentration. The radon concentration ranges between 0.1 and 48.6±1.7 Bq l -1 , while the radium concentration varies from a minimum detectable activity of -1 in Kutahya city. In addition to the radon and radium levels, parameters such as pH, conductivity and temperature of the water, humidity, pressure, elevation and the coordinates of the sampling points have also been measured and recorded. The annual effective dose from radon and radium due to typical water usage has been calculated. The resulting contribution to the annual effective dose due to radon ingestion varies between 0.3 and 124.2 μSv y -1 ; the contribution to the annual effective dose due to radium ingestion varies between 0 and 143.3 μSv y -1 ; the dose contribution to the stomach due to radon ingestion varies between 0.03 and 14.9 μSv y -1 . The dose contribution due to radon inhalation ranges between 0.3 and 122.5 μSv y -1 , assuming a typical transfer of radon in water to the air. For the overwhelming majority of the Kutahya population, it is determined that the average radiation exposure from drinking water is less than 73.6μmSv y -1 . (authors)

  13. Quantitative Detection of Trace Malachite Green in Aquiculture Water Samples by Extractive Electrospray Ionization Mass Spectrometry.

    Science.gov (United States)

    Fang, Xiaowei; Yang, Shuiping; Chingin, Konstantin; Zhu, Liang; Zhang, Xinglei; Zhou, Zhiquan; Zhao, Zhanfeng

    2016-08-11

    Exposure to malachite green (MG) may pose great health risks to humans; thus, it is of prime importance to develop fast and robust methods to quantitatively screen the presence of malachite green in water. Herein the application of extractive electrospray ionization mass spectrometry (EESI-MS) has been extended to the trace detection of MG within lake water and aquiculture water, due to the intensive use of MG as a biocide in fisheries. This method has the advantage of obviating offline liquid-liquid extraction or tedious matrix separation prior to the measurement of malachite green in native aqueous medium. The experimental results indicate that the extrapolated detection limit for MG was ~3.8 μg·L(-1) (S/N = 3) in lake water samples and ~0.5 μg·L(-1) in ultrapure water under optimized experimental conditions. The signal intensity of MG showed good linearity over the concentration range of 10-1000 μg·L(-1). Measurement of practical water samples fortified with MG at 0.01, 0.1 and 1.0 mg·L(-1) gave a good validation of the established calibration curve. The average recoveries and relative standard deviation (RSD) of malachite green in lake water and Carassius carassius fish farm effluent water were 115% (6.64% RSD), 85.4% (9.17% RSD) and 96.0% (7.44% RSD), respectively. Overall, the established EESI-MS/MS method has been demonstrated suitable for sensitive and rapid (malachite green in various aqueous media, indicating its potential for online real-time monitoring of real life samples.

  14. Report on water quality, sediment and water chemistry data for water and sediment samples collected from source areas to Melton Hill and Watts Bar reservoirs

    International Nuclear Information System (INIS)

    Tomaszewski, T.M.; Bruggink, D.J.; Nunn, D.L.

    1995-01-01

    Contamination of surface water and sediments in the Clinch River and Watts Bar Reservoir (CR/WBR) system as a result of past and present activities by the US Department of Energy (DOE) on the Oak Ridge Reservation (ORR) and also activities by non-ORR facilities are being studied by the Clinch River Environmental Restoration Program (CR-ERP). Previous studies have documented the presence of heavy metals, organics, and radionuclides in the sediments of reservoirs in the vicinity. In support of the CR-ERP, during the summer of 1991, TVA collected and evaluated water and sediment samples from swimming areas and municipal water intakes on Watts Bar Reservoir, Melton Hill Reservoir and Norris Reservoir, which was considered a source of less-contaminated reference or background data. Despite the numerous studies, until the current work documented by this report, relatively few sediment or water samples had been collected by the CR-ERP in the immediate vicinity of contaminant point sources. This work focused on water and sediment samples taken from points immediately downstream from suspected effluent point sources both on and off the ORR. In August and September, 1994, TVA sampled surface water and sediment at twelve locations in melton Hill and Watts Bar Reservoirs

  15. Fast and effective determination of strontium-90 in high volumes water samples

    International Nuclear Information System (INIS)

    Basarabova, B.; Dulanska, S.

    2014-01-01

    A simple and fast method was developed for determination of 90 Sr in high volumes of water samples from vicinity of nuclear power facilities. Samples were taken from the environment near Nuclear Power Plants in Jaslovske Bohunice and Mochovce in Slovakia. For determination of 90 Sr was used solid phase extraction using commercial sorbent Analig R Sr-01 from company IBC Advanced Technologies, Inc.. Determination of 90 Sr was performed with dilute solution of HNO 3 (1.5-2 M) and also tested in base medium with NaOH. For elution of 90 Sr was used eluent EDTA with pH in range 8-9. To achieve fast determination, automation was applied, which brings significant reduction of separation time. Concentration of water samples with evaporation was not necessary. Separation was performed immediately after filtration of analyzed samples. The aim of this study was development of less expensive, time unlimited and energy saving method for determination of 90 Sr in comparison with conventional methods. Separation time for fast-flow with volume of 10 dm 3 of water samples was 3.5 hours (flow-rate approximately 3.2 dm 3 / 1 hour). Radiochemical strontium yield was traced by using radionuclide 85 Sr. Samples were measured with HPGe detector (High-purity Germanium detector) at energy E φ = 514 keV. By using Analig R Sr-01 yields in range 72 - 96 % were achieved. Separation based on solid phase extraction using Analig R Sr-01 employing utilization of automation offers new, fast and effective method for determination of 90 Sr in water matrix. After ingrowth of yttrium samples were measured by Liquid Scintillation Spectrometer Packard Tricarb 2900 TR with software Quanta Smart. (authors)

  16. Evaluation of genotoxicity and cytotoxicity of water samples from the Sinos River Basin, southern Brazil

    Directory of Open Access Journals (Sweden)

    E Bianchi

    Full Text Available Some water bodies in the Sinos River Basin (SRB have been suffering the effects of pollution by residential, industrial and agroindustrial wastewater. The presence of cytotoxic and genotoxic compounds could compromise the water quality and the balance of these ecosystems. In this context, the research aimed to evaluate the genotoxicity and cytotoxicity of the water at four sites along the SRB (in the cities of Santo Antônio da Patrulha, Parobé, Campo Bom and Esteio, using bioassays in fish and cell culture. Samples of surface water were collected and evaluated in vitro using the Astyanax jacuhiensis fish species (micronucleus test and comet assay and the Vero lineage of cells (comet assay and cytotoxicity tests, neutral red - NR and tetrazolium MTT. The micronucleus test in fish showed no significant differences between the sampling sites, and neither did the comet assay and the MTT and NR tests in Vero cells. The comet assay showed an increase in genetic damage in the fish exposed to water samples collected in the middle and lower sections of the basin (Parobé, Campo Bom and Esteio when compared to the upper section of the basin (Santo Antônio da Patrulha. The results indicate contamination by genotoxic substances starting in the middle section of the SRB.

  17. The concentration of Cs, Sr and other elements in water samples collected in a paddy field

    International Nuclear Information System (INIS)

    Ban-nai, Tadaaki; Hisamatsu, Shun'ichi; Yanai-Kudo, Masumi; Hasegawa, Hidenao; Torikai, Yuji

    2000-01-01

    To research elemental concentrations in soil water in a paddy field, samples of the soil water were collected with porous Teflon resin tubes which were buried in the field. The soil water collections were made at various depth, 2.5, 12.5, 25 and 35 cm from the surface in the paddy field, located in Rokkasho, Aomori, once every two weeks during the rice cultivation period, from May to October in 1998. The paddy field was irrigated from May 7th to July 20th, dried from July 20th to August 5th, then again irrigated until September 16th. Drastic changes of the alkaline earth metal elements, Fe and Mn in soil water samples were seen at the beginning and end of the midsummer drainage. The concentrations of Cs, Fe, Mn and NH 4 in soil water samples showed a similar variation pattern to that of alkaline earth metal elements in the waterlogged period. The change of redox potential was considered a possible cause for the concentration variation for these substances. (author)

  18. Supplement to the UMTRA Project water sampling and analysis plan, Maybell, Colorado

    International Nuclear Information System (INIS)

    1995-09-01

    This water sampling and analysis plan (WSAP) supplement supports the regulatory and technical basis for water sampling at the Maybell, Colorado, Uranium Mill Tailings Remedial Action (UMTRA) Project site, as defined in the 1994 WSAP document for Maybell (DOE, 1994a). Further, this supplement serves to confirm our present understanding of the site relative to the hydrogeology and contaminant distribution as well as our intention to continue to use the sampling strategy as presented in the 1994 WSAP document for Maybell. Ground water and surface water monitoring activities are derived from the US Environmental Protection Agency regulations in 40 CFR Part 192 (1994) and 60 CFR 2854 (1 995). Sampling procedures are guided by the UMTRA Project standard operating procedures (JEG, n.d.), the Technical Approach Document (DOE, 1989), and the most effective technical approach for the site. Additional site-specific documents relevant to the Maybell site are the Maybell Baseline Risk Assessment (currently in progress), the Maybell Remedial Action Plan (RAP) (DOE, 1994b), and the Maybell Environmental Assessment (DOE, 1995)

  19. TECHNICAL FACT SHEET: A Systematic Evaluation of Dissolved Metals Loss during Water Sample Filtration

    Science.gov (United States)

    This research study examined how water quality collection and filtration approaches, including commonly used capsule and disc syringe filters, may cause losses in the amounts of soluble lead and copper found in a sample. A variety of commercially available filter materials with a...

  20. New technologies to detect and monitor Phytophthora ramorum in plant, soil, and water samples

    Science.gov (United States)

    Paul Russell; Nathan McOwen; Robert Bohannon

    2013-01-01

    The focus of our research efforts has been to develop methods to quickly identify plants, soil, and water samples infested with Phytophthora spp., and to rapidly confirm the findings using novel isothermal DNA technologies suitable for field use. These efforts have led to the development of a rapid Immunostrip® that reliably detects...

  1. RA-226 concentration in water samples near uranium mines and in marine fishes

    International Nuclear Information System (INIS)

    Porntepkasemsan, B.

    1987-11-01

    Radium-226 and calcium were measured in water samples from the vicinity of three uranium mines and in fish samples collected from Puget sound, Washington State. The radium content of the samples were below the maximum permissible concentration 3 pCi/L for drinking water recommended by the Public Health Service and U.S. Environmental Protection Agency. The mean value of Ra-226 in water was 0.428 pCi/L and ranged from 0.043 to 1.552 pCi/L, whereas calcium content ranged from 3.0 to 190.0 mg/L. Ra-226 concentrations and calcium content in whole fish were 0.833-20.328 pCi/kg wet wt. and 114.1-259.3 mg/g ash, respectively. Results of the study indicated that Ra-226 concentration in water was correlated with calcium concentration but that this correlation was not observed in fish sample except English sole

  2. HYDROLYSIS OF MTBE TO TBA IN GROUND WATER SAMPLES WITH HYDROCHLORIC ACID

    Science.gov (United States)

    Conventional sampling and analytical protocols have poor sensitivity for fuel oxygenates that are alcohols, such as tert-butyl alcohol (TBA). Because alcohols are miscible or highly soluble in water, alcohols are not efficiently transferred to the gas chromatograph for analysis....

  3. Trends in analytical methodologies for the determination of alkylphenols and bisphenol A in water samples.

    Science.gov (United States)

    Salgueiro-González, N; Muniategui-Lorenzo, S; López-Mahía, P; Prada-Rodríguez, D

    2017-04-15

    In the last decade, the impact of alkylphenols and bisphenol A in the aquatic environment has been widely evaluated because of their high use in industrial and household applications as well as their toxicological effects. These compounds are well-known endocrine disrupting compounds (EDCs) which can affect the hormonal system of humans and wildlife, even at low concentrations. Due to the fact that these pollutants enter into the environment through waters, and it is the most affected compartment, analytical methods which allow the determination of these compounds in aqueous samples at low levels are mandatory. In this review, an overview of the most significant advances in the analytical methodologies for the determination of alkylphenols and bisphenol A in waters is considered (from 2002 to the present). Sample handling and instrumental detection strategies are critically discussed, including analytical parameters related to quality assurance and quality control (QA/QC). Special attention is paid to miniaturized sample preparation methodologies and approaches proposed to reduce time- and reagents consumption according to Green Chemistry principles, which have increased in the last five years. Finally, relevant applications of these methods to the analysis of water samples are examined, being wastewater and surface water the most investigated. Copyright © 2017 Elsevier B.V. All rights reserved.

  4. Sample preparation for combined chemical analysis and bioassay application in water quality assessment

    NARCIS (Netherlands)

    Kolkman, A.; Schriks, M.; Brand, W; Bäuerlein, P.S.; van der Kooi, M.M.E.; van Doorn, R.H.; Emke, E.; Reus, A.; van der Linden, S.; de Voogt, P.; Heringa, M.B.

    2013-01-01

    The combination of in vitro bioassays and chemical screening can provide a powerful toolbox to determine biologically relevant compounds in water extracts. In this study, a sample preparation method is evaluated for the suitability for both chemical analysis and in vitro bioassays. A set of 39

  5. Water sampling at the Berge Helene FPSO at Chinguetti field in Mauritania using passive samplers

    NARCIS (Netherlands)

    Korytar, P.; Galien, van der W.

    2007-01-01

    Three rounds of water sampling were performed at the Berge Helene FPSO at the Chinguetti field in Mauritania using passive samplers attached to the FPSO to determine the levels of contamination that could potentially accumulate in organisms. Two rounds were carried out prior to the commencement of

  6. Innovative sampling and extraction methods for the determination of nonsteroidal anti-inflammatory drugs in water.

    Science.gov (United States)

    Tanwar, Shivani; Di Carro, Marina; Magi, Emanuele

    2015-03-15

    Two different innovative approaches were used for the determination of nonsteroidal anti-inflammatory drugs (NSAIDs) in water: stir bar sorptive extraction (SBSE) and passive sampling, followed by electrospray ionization liquid chromatography-tandem mass spectrometry. SBSE was developed by comparing EG-Silicone and PDMS stir bars and optimizing main parameters to attain high preconcentration. Quantitative analysis was carried out by mass spectrometry in negative ionization mode and multiple reaction monitoring. The SBSE-LC-MS/MS method provided satisfactory figures of merit with LOD (7.5-71 ng L(-1)) and LOQ (22.5-213 ng L(-1)). The developed method was successfully applied to real samples collected from river water and wastewater effluents. The obtained results showed the presence of all analytes at trace levels, in a wide range of concentrations. The passive sampling approach was carried out by using Polar Organic Chemical Integrative Sampler (POCIS); samplers were deployed for 15 days in river and tap water, allowing to detect analytes at ultra-trace levels. Time-Weighted Average concentration of NSAIDs in river water was estimated in the range 0.33-0.46 ng L(-1), using the sampling rates previously obtained by means of a simple calibration system. Copyright © 2014 Elsevier B.V. All rights reserved.

  7. Supplement to the UMTRA Project water sampling and analysis plan, Monument Valley, Arizona

    International Nuclear Information System (INIS)

    1995-09-01

    This water sampling and analysis plan (WSAP) supplement supports the regulatory and technical basis for water sampling at the Riverton, Wyoming, Uranium Mill Tailings Remedial Action (UMTRA) Project site, as defined in the 1994 WSAP document for Riverton (DOE, 1994). Further, the supplement serves to confirm the Project's present understanding of the site relative to the hydrogeology and contaminant distribution as well as the intent to continue to use the sampling strategy as presented in the 1994 WSAP document for Riverton. Ground water and surface water monitoring activities are derived from the US Environmental Protection Agency regulations in 40 CFR Part 192 and 60 FR 2854. Sampling procedures are guided by the UMTRA Project standard operating procedures (JEG, n.d.), the Technical Approach Document (DOE, 1989), and the most effective technical approach for the site. Additional site-specific documents relevant to the Riverton site are the Riverton Baseline Risk Assessment (BLRA) (DOE, 1995a) and the Riverton Site Observational Work Plan (SOWP) (DOE, 1995b)

  8. Evaluation of ELISA tests specific for Shiga toxin 1 and 2 in food and water samples

    Science.gov (United States)

    Two enzyme-linked immunosorbent assay (ELISA) kits were evaluated for their effectiveness in detecting and differentiating between Shiga toxin 1 and 2 (Stx1 and Stx2) produced by Shiga toxin-producing E. coli (STEC) inoculated into food and water samples. Each kit incorporated monoclonal antibodies ...

  9. Evaluation of HDPE water sample bottles and PVC sampler tubing used in herbicide dissipation studies.

    Science.gov (United States)

    J. B. Fischer; J. L. Michael; H. L. Gibbs

    2009-01-01

    The recovery of six herbicides (triclopyr, triclopyr ester, sulfometuron methyl, metsulfuron methyl, imazapyr, and hexazinone) was evaluated in two stream water samples, one from Weogufka Creek in the Alabama Piedmont and one from a stagnant stream in the Escambia Experimental Forest near Florida. Simulated field study conditions were...

  10. Corrosion of gadolinium aluminate-aluminium oxide samples in fully desalinated water at 575 K

    International Nuclear Information System (INIS)

    Hattenbach, K.; Zimmermann, H.U.

    1978-07-01

    Corrosion tests have been carried out for 1 1/2 years on gadolinium aluminate/aluminium oxide samples (burnable poison for ship propulsion reactors) with and without cans at 575 K in fully desalinated water. It was found that this substance is highly corrosion-resistant. (orig./HP) [de

  11. Supplement to the UMTRA Project water sampling and analysis plan, Mexican Hat, Utah

    International Nuclear Information System (INIS)

    1995-09-01

    This water sampling and analysis plan (WSAP) supplement supports the regulatory and technical basis for water sampling at the Mexican Hat, Utah, Uranium Mill Tailings Remedial Action (UMTRA) Project site, as defined in the 1994 WSAP document for Mexican Hat (DOE, 1994). Further, the supplement serves to confirm our present understanding of the site relative to the hydrogeology and contaminant distribution as well as our intention to continue to use the sampling strategy as presented in the 1994 WSAP document for Mexican Hat. Ground water and surface water monitoring activities are derived from the US Environmental Protection Agency regulations in 40 CFR Part 192 (1991) and 60 FR 2854 (1995). Sampling procedures are guided by the UMTRA Project standard operating procedures (JEG, n.d.), the Technical Approach Document (DOE, 1989), and the most effective technical approach for the site. Additional site-specific documents relevant to the Mexican Hat site are the Mexican Hat Long-Term Surveillance Plan (currently in progress), and the Mexican Hat Site Observational Work Plan (currently in progress)

  12. Evaluation of polyethersulfone performance for the microextraction of polar chlorinated herbicides from environmental water samples.

    Science.gov (United States)

    Prieto, Ailette; Rodil, Rosario; Quintana, José Benito; Cela, Rafael; Möder, Monika; Rodríguez, Isaac

    2014-05-01

    In this work, the suitability of bulk polyethersulfone (PES) for sorptive microextraction of eight polar, chlorinated phenoxy acids and dicamba from environmental water samples is assessed and the analytical features of the optimized method are compared to those reported for other microextraction techniques. Under optimized conditions, extractions were performed with samples (18 mL) adjusted at pH 2 and containing a 30% (w/v) of sodium chloride, using a tubular PES sorbent (1 cm length × 0.7 mm o.d., sorbent volume 8 µL). Equilibrium conditions were achieved after 3h of direct sampling, with absolute extraction efficiencies ranging from 39 to 66%, depending on the compound. Analytes were recovered soaking the polymer with 0.1 mL of ethyl acetate, derivatized and determined by gas chromatography-mass spectrometry (GC-MS). Achieved quantification limits (LOQs) varied between 0.005 and 0.073 ng mL(-1). After normalization with the internal surrogate (IS), the efficiency of the extraction was only moderately affected by the particular characteristics of different water samples (surface and sewage water); thus, pseudo-external calibration, using spiked ultrapure water solutions, can be used as quantification technique. The reduced cost of the PES polymer allowed considering it as a disposable sorbent, avoiding variations in the performance of the extraction due to cross-contamination problems and/or surface modification with usage. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. 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.

  14. 226Ra, 232Th and 40K analysis in water samples from Assiut, Egypt

    International Nuclear Information System (INIS)

    El-Gamal, H.; Abdel Mageed, A.I.; El-Attar, A.L; Abdel Hamid, M.

    2013-01-01

    The activity concentrations of 226 Ra, 232 Th and 40 K were determined in water samples, using 2”x 2” NaI(Tl) scintillation detector. Water activity ranges from 0.07 to 0.59 Bq L−1 for 226 Ra, 0.05 to 0.37 Bq L−1 for 232 Th and 3.25 to 8.72 Bq L−1 for 40 K with mean values of 2.64, 2.22 and 119.50 Bq L−1, respectively. As far as the measured gamma radionuclides is concerned, the mean annual effective doses for all analyzed samples of water are in the range of 0.02–0.08, 0.03-0.17 and 0.03-0.10 mSv yr -1 for infants, children and adults, respectively, all being lower than the reference level of the committed effective dose recommended by the WHO.

  15. Detection of Flavobacterium psychrophilum from fish tissue and water samples by PCR amplification

    DEFF Research Database (Denmark)

    Wiklund, T.; Madsen, Lone; Bruun, Morten Sichlau

    2000-01-01

    investigation, the possible detection of Fl. psychrophilum from fish tissue and water samples was examined using nested PCR with DNA probes against a sequence of the 16S rRNA genes. The DNA was extracted using Chelex(R) 100 chelating resin. The primers, which were tested against strains isolated from diseased...... fish, healthy fish, fish farm environments and reference strains, proved to be specific for Fl. psychrophilum. The obtained detection limit of Fl. psychrophilum seeded into rainbow trout brain tissue was 0.4 cfu in the PCR tube, corresponding to 17 cfu mg(-1) brain tissue. The PCR-assay proved...... to be more sensitive than agar cultivation of tissue samples from the brain of rainbow trout injected with Fl. psychrophilum. In non-sterile fresh water seeded with Fl. psychrophilum the detection limit of the PCR- assay was 1.7 cfu in the PCR tube, corresponding to 110 cfu ml(-1) water. The PCR...

  16. Radium 226 and lead 210 water extraction from mill tailings samples

    International Nuclear Information System (INIS)

    Fourcade, N.; Zettwoog, P.; Mery, G.

    1994-01-01

    Depositories for waste from the processing of uranium ore may release seepage waters into the environment through their impoundments. Seepage waters, when percolating through the wastes, extract radium 226. In the design or rehabilitation stage of such depositories, the exposure of critical groups of the population to radium 226 from the ground water pathway must be assessed. The same applies to lead 210. The first step is to assess the possibility of extracting the radium 226 and the lead 210 from samples of solid wastes and sludges in laboratory tests using water from the site. Extensive tests of this type were carried out in our laboratories between 1982 and 1991 on samples of mill tailings which had been collected in six installations of COGEMA and its subsidiaries. The main results are presented and analyzed. Physical, chemical and mineralogical factors influencing the leaching rates and the total quantity of water-extractable radium 226 are identified. In the case of a wet storage option, a tentative modelling of the water extraction phenomenon is proposed for the prediction of the source term both in the short term, and in the long term when all more or less soluble salts have been eliminated from the solid wastes

  17. Determination of air-loop volume and radon partition coefficient for measuring radon in water sample.

    Science.gov (United States)

    Lee, Kil Yong; Burnett, William C

    A simple method for the direct determination of the air-loop volume in a RAD7 system as well as the radon partition coefficient was developed allowing for an accurate measurement of the radon activity in any type of water. The air-loop volume may be measured directly using an external radon source and an empty bottle with a precisely measured volume. The partition coefficient and activity of radon in the water sample may then be determined via the RAD7 using the determined air-loop volume. Activity ratios instead of absolute activities were used to measure the air-loop volume and the radon partition coefficient. In order to verify this approach, we measured the radon partition coefficient in deionized water in the temperature range of 10-30 °C and compared the values to those calculated from the well-known Weigel equation. The results were within 5 % variance throughout the temperature range. We also applied the approach for measurement of the radon partition coefficient in synthetic saline water (0-75 ppt salinity) as well as tap water. The radon activity of the tap water sample was determined by this method as well as the standard RAD-H 2 O and BigBottle RAD-H 2 O. The results have shown good agreement between this method and the standard methods.

  18. Determination of air-loop volume and radon partition coefficient for measuring radon in water sample

    International Nuclear Information System (INIS)

    Kil Yong Lee; Burnett, W.C.

    2013-01-01

    A simple method for the direct determination of the air-loop volume in a RAD7 system as well as the radon partition coefficient was developed allowing for an accurate measurement of the radon activity in any type of water. The air-loop volume may be measured directly using an external radon source and an empty bottle with a precisely measured volume. The partition coefficient and activity of radon in the water sample may then be determined via the RAD7 using the determined air-loop volume. Activity ratios instead of absolute activities were used to measure the air-loop volume and the radon partition coefficient. In order to verify this approach, we measured the radon partition coefficient in deionized water in the temperature range of 10-30 deg C and compared the values to those calculated from the well-known Weigel equation. The results were within 5 % variance throughout the temperature range. We also applied the approach for measurement of the radon partition coefficient in synthetic saline water (0-75 ppt salinity) as well as tap water. The radon activity of the tap water sample was determined by this method as well as the standard RAD-H 2 O and BigBottle RAD-H 2 O. The results have shown good agreement between this method and the standard methods. (author)

  19. Letter Report: Stable Hydrogen and Oxygen Isotope Analysis of B-Complex Perched Water Samples

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Brady D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Moran, James J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Nims, Megan K. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Saunders, Danielle L. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2017-04-13

    Fine-grained sediments associated with the Cold Creek Unit at Hanford have caused the formation of a perched water aquifer in the deep vadose zone at the B Complex area, which includes waste sites in the 200-DV-1 Operable Unit and the single-shell tank farms in Waste Management Area B-BX-BY. High levels of contaminants, such as uranium, technetium-99, and nitrate, make this aquifer a continuing source of contamination for the groundwater located a few meters below the perched zone. Analysis of deuterium (2H) and 18-oxygen (18O) of nine perched water samples from three different wells was performed. Samples represent time points from hydraulic tests performed on the perched aquifer using the three wells. The isotope analyses showed that the perched water had δ2H and δ18O ratios consistent with the regional meteoric water line, indicating that local precipitation events at the Hanford site likely account for recharge of the perched water aquifer. Data from the isotope analysis can be used along with pumping and recovery data to help understand the perched water dynamics related to aquifer size and hydraulic control of the aquifer in the future.

  20. An Energy Efficient Adaptive Sampling Algorithm in a Sensor Network for Automated Water Quality Monitoring.

    Science.gov (United States)

    Shu, Tongxin; Xia, Min; Chen, Jiahong; Silva, Clarence de

    2017-11-05

    Power management is crucial in the monitoring of a remote environment, especially when long-term monitoring is needed. Renewable energy sources such as solar and wind may be harvested to sustain a monitoring system. However, without proper power management, equipment within the monitoring system may become nonfunctional and, as a consequence, the data or events captured during the monitoring process will become inaccurate as well. This paper develops and applies a novel adaptive sampling algorithm for power management in the automated monitoring of the quality of water in an extensive and remote aquatic environment. Based on the data collected on line using sensor nodes, a data-driven adaptive sampling algorithm (DDASA) is developed for improving the power efficiency while ensuring the accuracy of sampled data. The developed algorithm is evaluated using two distinct key parameters, which are dissolved oxygen (DO) and turbidity. It is found that by dynamically changing the sampling frequency, the battery lifetime can be effectively prolonged while maintaining a required level of sampling accuracy. According to the simulation results, compared to a fixed sampling rate, approximately 30.66% of the battery energy can be saved for three months of continuous water quality monitoring. Using the same dataset to compare with a traditional adaptive sampling algorithm (ASA), while achieving around the same Normalized Mean Error (NME), DDASA is superior in saving 5.31% more battery energy.

  1. High-resolution passive sampling of dissolved methane in the water column of lakes in Greenland

    Science.gov (United States)

    Goldman, A. E.; Cadieux, S. B.; White, J. R.; Pratt, L. M.

    2013-12-01

    Arctic lakes are important participants in the global carbon cycle, releasing methane in a warming climate and contributing to a positive feedback to climate change. In order to yield detailed methane budgets and understand the implications of warming on methane dynamics, high-resolution profiles revealing methane behavior within the water column need to be obtained. Single day sampling using disruptive techniques has the potential to result in biases. In order to obtain high-resolution, undisturbed profiles of methane concentration and isotopic composition, this study evaluates a passive sampling method over a multi-day equilibration period. Selected for this study were two small lakes (Gatos Research Methane Carbon Isotope Analyzer. PDB sampling and pump sampling resulted in statistically similar concentrations (R2=0.89), ranging from 0.85 to 135 uM from PDB and 0.74 to 143 uM from pump sampling. In anoxic waters of the lake, where concentrations were high enough to yield robust isotopic results on the LGR MCIA, δ13C were also similar between the two methods, yielding -73‰ from PDB and -74‰ from pump sampling. Further investigation will produce results for a second lake and methane carbon and hydrogen isotopic composition for both lakes. Preliminary results for this passive sampling method are promising. We envision the use of this technique in future studies of dissolved methane and expect that it will provide a more finely resolved vertical profile, allowing for a more complete understanding of lacustrine methane dynamics.

  2. An Energy Efficient Adaptive Sampling Algorithm in a Sensor Network for Automated Water Quality Monitoring

    Directory of Open Access Journals (Sweden)

    Tongxin Shu

    2017-11-01

    Full Text Available Power management is crucial in the monitoring of a remote environment, especially when long-term monitoring is needed. Renewable energy sources such as solar and wind may be harvested to sustain a monitoring system. However, without proper power management, equipment within the monitoring system may become nonfunctional and, as a consequence, the data or events captured during the monitoring process will become inaccurate as well. This paper develops and applies a novel adaptive sampling algorithm for power management in the automated monitoring of the quality of water in an extensive and remote aquatic environment. Based on the data collected on line using sensor nodes, a data-driven adaptive sampling algorithm (DDASA is developed for improving the power efficiency while ensuring the accuracy of sampled data. The developed algorithm is evaluated using two distinct key parameters, which are dissolved oxygen (DO and turbidity. It is found that by dynamically changing the sampling frequency, the battery lifetime can be effectively prolonged while maintaining a required level of sampling accuracy. According to the simulation results, compared to a fixed sampling rate, approximately 30.66% of the battery energy can be saved for three months of continuous water quality monitoring. Using the same dataset to compare with a traditional adaptive sampling algorithm (ASA, while achieving around the same Normalized Mean Error (NME, DDASA is superior in saving 5.31% more battery energy.

  3. Results of elemental analyses of water and waterborne sediment samples from the Fairbanks NTMS quadrangle, Alaska

    International Nuclear Information System (INIS)

    Sharp, R.R. Jr.; Aamodt, P.L; Hill, D.E.

    1979-04-01

    During the late spring and then again in late summer, 1977, lake and stream water and bottom sediment samples were collected at a nominal density of one location every 16 km 2 from throughout the approximate 16,500-km 2 area of the Fairbanks NTMS quadrangle, Alaska. These samples were collected using standard procedures by investigators from the University of Alaska, Fairbanks, as part of a special Hydrogeochemical and Stream Sediment Reconnaissance (HSSR) study to identify variance in total uranium contents related to natural factors such as seasonal changes, source types, and geologic/geographic environments. Histograms and statistical summaries of total uranium in a number of sample populations presented herein indicate that water samples collected in late summer have a mean uranium content that is slightly higher than the mean for waters collected in the spring. Dilution and/or evaporative concentration are possible causes for this difference. Sediment samples collected from streams and springs have a slightly higher mean uranium content than those collected from lakes, and this is consistent with HSSR data from other Alaskan areas. The Alaskan investigators will complete a detailed analysis of variance study of these data in the near future and a second open-file report will be forthcoming upon its completion

  4. Summary of Inorganic Compositional Data for Groundwater, Soil-Water, and Surface-Water Samples at the Headgate Draw Subsurface Drip Irrigation Site

    Energy Technology Data Exchange (ETDEWEB)

    Geboy, Nicholas J.; Engle, Mark A.; Schroeder, Karl T.; Zupanic, John W.

    2007-01-01

    As part of a 5-year project on the impact of subsurface drip irrigation (SDI) application of coalbed-methane (CBM) produced waters, water samples were collected from the Headgate Draw SDI site in the Powder River Basin, Wyoming, USA. This research is part of a larger study to understand short- and long-term impacts on both soil and water quality from the beneficial use of CBM waters to grow forage crops through use of SDI. This document provides a summary of the context, sampling methodology, and quality assurance and quality control documentation of samples collected prior to and over the first year of SDI operation at the site (May 2008-October 2009). This report contains an associated database containing inorganic compositional data, water-quality criteria parameters, and calculated geochemical parameters for samples of groundwater, soil water, surface water, treated CBM waters, and as-received CBM waters collected at the Headgate Draw SDI site.

  5. Determination of colloidal and dissolved silver in water samples using colorimetric solid-phase extraction.

    Science.gov (United States)

    Hill, April A; Lipert, Robert J; Porter, Marc D

    2010-03-15

    The increase in bacterial resistance to antibiotics has led to resurgence in the use of silver as a biocidal agent in applications ranging from washing machine additives to the drinking water treatment system on the International Space Station (ISS). However, growing concerns about the possible toxicity of colloidal silver to bacteria, aquatic organisms and humans have led to recently issued regulations by the US EPA and FDA regarding the usage of silver. As part of an ongoing project, we have developed a rapid, simple method for determining total silver, both ionic (silver(I)) and colloidal, in 0.1-1mg/L aqueous samples, which spans the ISS potable water target of 0.3-0.5mg/L (total silver) and meets the US EPA limit of 0.1mg/L in drinking water. The method is based on colorimetric solid-phase extraction (C-SPE) and involves the extraction of silver(I) from water samples by passage through a solid-phase membrane impregnated with the colorimetric reagent DMABR (5-[4-(dimethylamino)benzylidene]rhodanine). Silver(I) exhaustively reacts with impregnated DMABR to form a colored compound, which is quantified using a handheld diffuse reflectance spectrophotometer. Total silver is determined by first passing the sample through a cartridge containing Oxone, which exhaustively oxidizes colloidal silver to dissolved silver(I). The method, which takes less than 2 min to complete and requires only approximately 1 mL of sample, has been validated through a series of tests, including a comparison with the ICP-MS analysis of a water sample from ISS that contained both silver(I) and colloidal silver. Potential earth-bound applications are also briefly discussed. Copyright (c) 2009 Elsevier B.V. All rights reserved.

  6. Daily variations of delta 18O and delta D in daily samplings of air water vapour and rain water in the Amazon Basin

    International Nuclear Information System (INIS)

    Matsui, E.; Salati, E.; Ribeiro, M.N.G.; Tancredi, A.C.F.N.S.; Reis, C.M. dos

    1984-01-01

    The movement of rain water in the soil from 0 to 120 cm depth using delta 18 O weekly variations is studied. A study of the delta D variability in water vapour and rain water samples during precipitation was also done, the samples being collected a 3 minute intervals from the beginning to the end of precipitation. (M.A.C.) [pt

  7. Application of empore TM strontium rad disks to the analysis of radiostrontium in environmental water samples

    International Nuclear Information System (INIS)

    Smith, L.L.; Seely, D.C.; Shannon, R.T.

    1996-01-01

    A solid phase extraction method for analyzing radioactive strontium in surface, ground, and drinking waters is presented. Strontium is simply isolated by pulling an acidified sample aliquot through an Empore TM strontium rad disk with a vacuum, and the disk is subsequently assayed for beta activity. The method is efficient, safe, reliable, and potentially field deployable. Sample preparation and counting source preparation may be condensed into a single procedure, thereby improving efficiency and eliminating many potential sources of laboratory error. Moreover, many of the hazardous chemicals associated with traditional strontium procedures are eliminated. Samples are easily batched, and a one-liter sample may be prepared with as little as 20 min of effort. For a one-liter aqueous sample, up to 3 mg of strontium can be retained by the disks. Chemical and radiometric interferences are discussed. (orig.)

  8. Sensitivity analysis using contribution to sample variance plot: Application to a water hammer model

    International Nuclear Information System (INIS)

    Tarantola, S.; Kopustinskas, V.; Bolado-Lavin, R.; Kaliatka, A.; Ušpuras, E.; Vaišnoras, M.

    2012-01-01

    This paper presents “contribution to sample variance plot”, a natural extension of the “contribution to the sample mean plot”, which is a graphical tool for global sensitivity analysis originally proposed by Sinclair. These graphical tools have a great potential to display graphically sensitivity information given a generic input sample and its related model realizations. The contribution to the sample variance can be obtained at no extra computational cost, i.e. from the same points used for deriving the contribution to the sample mean and/or scatter-plots. The proposed approach effectively instructs the analyst on how to achieve a targeted reduction of the variance, by operating on the extremes of the input parameters' ranges. The approach is tested against a known benchmark for sensitivity studies, the Ishigami test function, and a numerical model simulating the behaviour of a water hammer effect in a piping system.

  9. Pre-concentration of uranium from water samples by dispersive liquid-liquid micro-extraction

    Energy Technology Data Exchange (ETDEWEB)

    Khajeh, Mostafa; Nemch, Tabandeh Karimi [Zabol Univ. (Iran, Islamic Republic of). Dept. of Chemistry

    2014-07-01

    In this study, a simple and rapid dispersive liquid-liquid microextraction (DLLME) was developed for the determination of uranium in water samples prior to high performance liquid chromatography with diode array detection. 1-(2-pyridylazo)-2-naphthol (PAN) was used as complexing agent. The effect of various parameters on the extraction step including type and volume of extraction and dispersive solvents, pH of solution, concentration of PAN, extraction time, sample volume and ionic strength were studied and optimized. Under the optimum conditions, the limit of detection (LOD) and preconcentration factor were 0.3 μg L{sup -1} and 194, respectively. Furthermore, the relative standard deviation of the ten replicate was <2.6%. The developed procedure was then applied to the extraction and determination of uranium in the water samples.

  10. Pre-concentration of uranium from water samples by dispersive liquid-liquid micro-extraction

    International Nuclear Information System (INIS)

    Khajeh, Mostafa; Nemch, Tabandeh Karimi

    2014-01-01

    In this study, a simple and rapid dispersive liquid-liquid microextraction (DLLME) was developed for the determination of uranium in water samples prior to high performance liquid chromatography with diode array detection. 1-(2-pyridylazo)-2-naphthol (PAN) was used as complexing agent. The effect of various parameters on the extraction step including type and volume of extraction and dispersive solvents, pH of solution, concentration of PAN, extraction time, sample volume and ionic strength were studied and optimized. Under the optimum conditions, the limit of detection (LOD) and preconcentration factor were 0.3 μg L -1 and 194, respectively. Furthermore, the relative standard deviation of the ten replicate was <2.6%. The developed procedure was then applied to the extraction and determination of uranium in the water samples.

  11. Radiological study of brackish and fresh water food samples in Lagos and Ondo states, southwestern Nigeria

    International Nuclear Information System (INIS)

    Ojo, T.J.; Ojo, O.C.

    2007-01-01

    Measurement of the average radioactivity concentration in brackish and fresh water food samples in Lagos and Ondo States of Nigeria was carried out using a very sensitive gamma spectroscopic system consisting of a 76 mm x 76 mm Nal (TI) scintillation detector coupled to a computerized ACCUSPEC installation. All the radionuclide detected are traceable to the naturally occurring 4 ''0K and ''2''3''2Th. The average concentrations of ''2''3''8U and ''2''3''2Th were found to be higher in brackish water food samples, 50.92±7.04 Bq/kg and 24.60± 6.47 Bq/kg respectively. The average concentration of ''4''0K was found to be higher in food samples got from freshwater, 738.94±84.81Bq/kg

  12. Variation of the 18O/16O ratio in water samples from branches

    International Nuclear Information System (INIS)

    Foerstel, H.; Huetzen, H.

    1979-06-01

    The studies of the water turnover of plants may use the labelling of water by its natural variation of the 18 O/ 16 O ratio. The basic value of such a study is the isotope ratio in soil water, which is represented by the 18 O/ 16 O ratio in water samples from stem and branches, too. During the water transport from the soil water reservoir to the leaves of trees, no fractionation of the oxygen isotopes occurs. The oxygen isotope ratio within a single twig varies about +- 0 / 00 (variation given as standard deviation of the delta-values), within the stem of a large tree about +- 2 0 / 00 . The results of water from stems of different trees at the site of the Nuclear Research Center Juelich scatter about +- 1 0 / 00 . The delta-values from a larger area (Rur valley-Eifel hills-Mosel valley), which were collected in October 1978 during the end of the vegetation period, showed a standard deviation between +- 2.2 (Rur valley) and +- 3.6 0 / 00 (Eifel hills). The 18 O/ 16 O-delta-values of a beech wood from Juelich site are in the range of - 7.3 and - 10.1 0 / 00 (mean local precipitation 1974 - 1977: - 7.4 0 / 00 ). At the hill site near Cologne (Bergisches Land, late September 1978) we observed an oxygen isotope ratio of - 9.1 0 / 00 (groundwater at the neighbourhood between - 7.6 and 8.7 0 / 00 ). In October 1978 at an area from the Netherlands to the Mosel valley we found delta-values of branch water between - 13.9 (lower Ruhr valley) and - 13.1 (Eifel hills to Mosel valley) in comparison to groundwater samples from the same region: - 7.55 and - 8.39. There was no significant difference between delta-values from various species or locations within this area. Groundwater samples should normally represent the 18 O/ 16 O ratio of local precipitation. The low delta-values of branch water could be due to the rapid uptake of precipitation water of low 18 O content in autumn to the water transport system of plants. (orig.) [de

  13. Sorption of polycyclic aromatic hydrocarbons (PAH) during the filtration of water samples

    International Nuclear Information System (INIS)

    Herbert, M.; Schueth, C.; Pyka, W.

    1992-01-01

    Filtration experiments were preformed for three selected polycyclic aromatic hydrocarbons (PAH-Fluorene, Fluoranthene and Benz(b)-fluoranthene) dissolved in water by varying filter materials, filter-pore sizes and filter equipment. The rate of recovery of PAH depended on the materials and methods applied. Organic filter materials showed a by far stronger sorption than inorganic materials. The losses for organic filters increased up to 100% with decreasing pore-size. The percentage loss was observed to increase with increasing octanol-water distribution coefficient (K OW ). Saturation tests revealed that the amount of water, necessary to saturate the filtration apparatus with and without filter-paper, also increased with the K OW . For BBF several liters would be necessary for saturation. It can be concluded, that the filtration of water samples, analysed for PAH, can lead to considerable errors in the analytical results, particularly for those PAH with log K OW larger than 5. (orig.)

  14. Comparative study of uranium concentration in water samples of SW and NE Punjab, India

    International Nuclear Information System (INIS)

    Saini, Komal; Bajwa, B.S.

    2014-01-01

    Since the commencement of the earth, radiations and natural radioactivity has always been a part of environment. Uranium is heaviest naturally occurring element which is widespread in nature, mainly occurs in granites mineral deposits. The natural weathering of rocks such as granite dissolves the natural uranium, which goes into groundwater by leaching and precipitation called illumination process. People are always exposed to certain amount of uranium from air, water, soil and food as it is usually present in these components. About 85% of ingested uranium enter into human body through drinking water which makes it very important to estimate uranium concentration in potable water. Uranium and some other heavy metals may increase the risk of kidney damage, cancer diseases where experimental evidence suggests that respiratory and reproductive system are also affected by uranium exposure. In the present study comparative study of uranium concentration in potable water samples of SW and NE Punjab has been analysed

  15. The origin of water in the primitive Moon as revealed by the lunar highlands samples

    Science.gov (United States)

    Barnes, Jessica J.; Tartèse, Romain; Anand, Mahesh; McCubbin, Francis M.; Franchi, Ian A.; Starkey, Natalie A.; Russell, Sara S.

    2014-03-01

    The recent discoveries of hydrogen (H) bearing species on the lunar surface and in samples derived from the lunar interior have necessitated a paradigm shift in our understanding of the water inventory of the Moon, which was previously considered to be a ‘bone-dry’ planetary body. Most sample-based studies have focused on assessing the water contents of the younger mare basalts and pyroclastic glasses, which are partial-melting products of the lunar mantle. In contrast, little attention has been paid to the inventory and source(s) of water in the lunar highlands rocks which are some of the oldest and most pristine materials available for laboratory investigations, and that have the potential to reveal the original history of water in the Earth-Moon system. Here, we report in-situ measurements of hydroxyl (OH) content and H isotopic composition of the mineral apatite from four lunar highlands samples (two norites, a troctolite, and a granite clast) collected during the Apollo missions. Apart from troctolite in which the measured OH contents in apatite are close to our analytical detection limit and its H isotopic composition appears to be severely compromised by secondary processes, we have measured up to ˜2200 ppm OH in the granite clast with a weighted average δD of ˜ -105±130‰, and up to ˜3400 ppm OH in the two norites (77215 and 78235) with weighted average δD values of -281±49‰ and -27±98‰, respectively. The apatites in the granite clast and the norites are characterised by higher OH contents than have been reported so far for highlands samples, and have H isotopic compositions similar to those of terrestrial materials and some carbonaceous chondrites, providing one of the strongest pieces of evidence yet for a common origin for water in the Earth-Moon system. In addition, the presence of water, of terrestrial affinity, in some samples of the earliest-formed lunar crust suggests that either primordial terrestrial water survived the aftermath

  16. Analysis of ground water and soil samples from severely arsenic affected blocks of Murshidabad district

    Directory of Open Access Journals (Sweden)

    Manali Biswas

    2017-10-01

    Full Text Available Contamination of groundwater and soil by arsenic is a serious threat to existence of mankind on the globe. Arsenic contaminates soil and groundwater by natural biogeochemical cycles. However, due to anthropogenic activities like indiscriminant use of arsenic in disinfectants, weedicides, medicines and fertilizers, arsenic toxicity is a severe environmental issue, both at national and global level. U.S. Environmental Protection Agency and World Health Organization prescribed the permissible limit of arsenic in drinking water to be 10 µg/l. Exposure to arsenic at higher levels over a considerable period of time leads to skin lesions and cancer, disorders of cardiovascular, respiratory, gastrointestinal, hepatic and renal systems. Murshidabad is one of the severely arsenic affected districts of West Bengal. We have analyzed soil and groundwater samples from some of the highly arsenic affected blocks of Murshidabad district. Both the soil and groundwater samples have an alkaline pH, a characteristic of the presence of arsenic in the tested samples. Unfortunately, the socio-economic conditions of these villages force the residents to use groundwater as the source of drinking water. Presence of considerably high amount of total dissolved solids in water samples make them further unfit for consumption. High amount of phosphate and iron present in some of the water samples takes a toll on the detoxification and excretory system of the body, if those water samples are consumed on a regular manner. Contamination of soil by the aforesaid contaminants results in biomagnification of these pollutants in the food chain. We could also isolate certain potentially arsenic resistant bacteria from the contaminated soil and water samples. At the next level we have surveyed an arsenic affected village to analyze the clinical manifestation of arsenic poisoning. In this village subjects developed rampant skin lesions throughout the body due to exposure to arsenic

  17. Autonomous water sampling for long-term monitoring of trace metals in remote environments.

    Science.gov (United States)

    Kim, Hyojin; Bishop, James K B; Wood, Todd J; Fung, Inez Y

    2012-10-16

    A remotely controlled autonomous method for long-term high-frequency sampling of environmental waters in remote locations is described. The method which preserves sample integrity of dissolved trace metals and major ions for month-long periods employs a gravitational filtration system (GFS) that separates dissolved and particulate phases as samples are collected. The key elements of GFS are (1) a modified "air-outlet" filter holder to maximize filtration rate and thus minimize filtration artifacts; and (2) the direct delivery of filtrate to dedicated bottle sets for specific analytes. Depth and screen filter types were evaluated with depth filters showing best performance. GFS performance is validated using ground, stream, and estuary waters. Over 30 days of storage, samples with GFS treatment had average recoveries of 95 ± 19% and 105 ± 7% of Fe and Mn, respectively; without GFS treatment, average recoveries were only 16% and 18%. Dissolved major cations K, Mg, and Na were stable independent of collection methodology, whereas Ca in some groundwater samples decreased up to 42% without GFS due to CaCO(3) precipitation. In-field performance of GFS equipped autosamplers is demonstrated using ground and streamwater samples collected at the Angelo Coast Range Reserve, California from October 3 to November 4 2011.

  18. Microwave-assisted headspace single-drop microextration of chlorobenzenes from water samples

    Energy Technology Data Exchange (ETDEWEB)

    Vidal, Lorena [Departamento de Quimica Analitica, Nutricion y Bromatologia, Universidad de Alicante, P.O. Box 99, E-03080 Alicante (Spain); Domini, Claudia E. [Departamento de Quimica Analitica, Nutricion y Bromatologia, Universidad de Alicante, P.O. Box 99, E-03080 Alicante (Spain); Grane, Nuria [Departamento de Quimica Analitica, Nutricion y Bromatologia, Universidad de Alicante, P.O. Box 99, E-03080 Alicante (Spain); Psillakis, Elefteria [Department of Environmental Engineering, Technical University of Crete, Polytechneioupolis, GR-73100 Chania, Crete (Greece); Canals, Antonio [Departamento de Quimica Analitica, Nutricion y Bromatologia, Universidad de Alicante, P.O. Box 99, E-03080 Alicante (Spain)]. E-mail: a.canals@ua.es

    2007-05-29

    A one-step and in-situ sample preparation method used for quantifying chlorobenzene compounds in water samples has been developed, coupling microwave and headspace single-drop microextraction (MW-HS-SDME). The chlorobenzenes in water samples were extracted directly onto an ionic liquid single-drop in headspace mode under the aid of microwave radiation. For optimization, a Plackett-Burman screening design was initially used, followed by a mixed-level factorial design. The factors considered were: drop volume, aqueous sample volume, stirring speed, ionic strength, extraction time, ionic liquid type, microwave power and length of the Y-shaped glass-tube. The optimum experimental conditions found from this statistical evaluation were: a 5 {mu}L microdrop of 1-hexyl-3-methylimidazolium hexafluorophosphate exposed for 20 min to the headspace of a 30 mL aqueous sample, irradiated by microwaves at 200 W and placed in a 50 mL spherical flask connected to a 25 cm Y-shaped glass-tube. Under the optimised experimental conditions, the response of a high performance liquid chromatographic system was found to be linear over the range studied and with correlation coefficients ranging between 0.9995 and 0.9999. The method showed a good level of repeatability, with relative standard deviations varying between 2.3 and 8.3% (n = 5). Detection limits were found in the low {mu}g L{sup -1} range varying between 0.016 and 0.039 {mu}g L{sup -1}. Overall, the performance of the proposed method demonstrated the favourable effect of microwave sample irradiation upon HS-SDME. Finally, recovery studies from different types of environmental water samples revealed that matrix had little effect upon extraction.

  19. Microwave-assisted headspace single-drop microextration of chlorobenzenes from water samples

    International Nuclear Information System (INIS)

    Vidal, Lorena; Domini, Claudia E.; Grane, Nuria; Psillakis, Elefteria; Canals, Antonio

    2007-01-01

    A one-step and in-situ sample preparation method used for quantifying chlorobenzene compounds in water samples has been developed, coupling microwave and headspace single-drop microextraction (MW-HS-SDME). The chlorobenzenes in water samples were extracted directly onto an ionic liquid single-drop in headspace mode under the aid of microwave radiation. For optimization, a Plackett-Burman screening design was initially used, followed by a mixed-level factorial design. The factors considered were: drop volume, aqueous sample volume, stirring speed, ionic strength, extraction time, ionic liquid type, microwave power and length of the Y-shaped glass-tube. The optimum experimental conditions found from this statistical evaluation were: a 5 μL microdrop of 1-hexyl-3-methylimidazolium hexafluorophosphate exposed for 20 min to the headspace of a 30 mL aqueous sample, irradiated by microwaves at 200 W and placed in a 50 mL spherical flask connected to a 25 cm Y-shaped glass-tube. Under the optimised experimental conditions, the response of a high performance liquid chromatographic system was found to be linear over the range studied and with correlation coefficients ranging between 0.9995 and 0.9999. The method showed a good level of repeatability, with relative standard deviations varying between 2.3 and 8.3% (n = 5). Detection limits were found in the low μg L -1 range varying between 0.016 and 0.039 μg L -1 . Overall, the performance of the proposed method demonstrated the favourable effect of microwave sample irradiation upon HS-SDME. Finally, recovery studies from different types of environmental water samples revealed that matrix had little effect upon extraction

  20. Evaluation of wastewater contaminant transport in surface waters using verified Lagrangian sampling

    Science.gov (United States)

    Antweiler, Ronald C.; Writer, Jeffrey H.; Murphy, Sheila F.

    2014-01-01

    Contaminants released from wastewater treatment plants can persist in surface waters for substantial distances. Much research has gone into evaluating the fate and transport of these contaminants, but this work has often assumed constant flow from wastewater treatment plants. However, effluent discharge commonly varies widely over a 24-hour period, and this variation controls contaminant loading and can profoundly influence interpretations of environmental data. We show that methodologies relying on the normalization of downstream data to conservative elements can give spurious results, and should not be used unless it can be verified that the same parcel of water was sampled. Lagrangian sampling, which in theory samples the same water parcel as it moves downstream (the Lagrangian parcel), links hydrologic and chemical transformation processes so that the in-stream fate of wastewater contaminants can be quantitatively evaluated. However, precise Lagrangian sampling is difficult, and small deviations – such as missing the Lagrangian parcel by less than 1 h – can cause large differences in measured concentrations of all dissolved compounds at downstream sites, leading to erroneous conclusions regarding in-stream processes controlling the fate and transport of wastewater contaminants. Therefore, we have developed a method termed “verified Lagrangian” sampling, which can be used to determine if the Lagrangian parcel was actually sampled, and if it was not, a means for correcting the data to reflect the concentrations which would have been obtained had the Lagrangian parcel been sampled. To apply the method, it is necessary to have concentration data for a number of conservative constituents from the upstream, effluent, and downstream sites, along with upstream and effluent concentrations that are constant over the short-term (typically 2–4 h). These corrections can subsequently be applied to all data, including non-conservative constituents. Finally, we

  1. Evaluation of wastewater contaminant transport in surface waters using verified Lagrangian sampling.

    Science.gov (United States)

    Antweiler, Ronald C; Writer, Jeffrey H; Murphy, Sheila F

    2014-02-01

    Contaminants released from wastewater treatment plants can persist in surface waters for substantial distances. Much research has gone into evaluating the fate and transport of these contaminants, but this work has often assumed constant flow from wastewater treatment plants. However, effluent discharge commonly varies widely over a 24-hour period, and this variation controls contaminant loading and can profoundly influence interpretations of environmental data. We show that methodologies relying on the normalization of downstream data to conservative elements can give spurious results, and should not be used unless it can be verified that the same parcel of water was sampled. Lagrangian sampling, which in theory samples the same water parcel as it moves downstream (the Lagrangian parcel), links hydrologic and chemical transformation processes so that the in-stream fate of wastewater contaminants can be quantitatively evaluated. However, precise Lagrangian sampling is difficult, and small deviations - such as missing the Lagrangian parcel by less than 1h - can cause large differences in measured concentrations of all dissolved compounds at downstream sites, leading to erroneous conclusions regarding in-stream processes controlling the fate and transport of wastewater contaminants. Therefore, we have developed a method termed "verified Lagrangian" sampling, which can be used to determine if the Lagrangian parcel was actually sampled, and if it was not, a means for correcting the data to reflect the concentrations which would have been obtained had the Lagrangian parcel been sampled. To apply the method, it is necessary to have concentration data for a number of conservative constituents from the upstream, effluent, and downstream sites, along with upstream and effluent concentrations that are constant over the short-term (typically 2-4h). These corrections can subsequently be applied to all data, including non-conservative constituents. Finally, we show how data

  2. Chemical and Microbiological Analysis of Certain Water Sources and Industrial Wastewater Samples in Dakahlia Governorate

    International Nuclear Information System (INIS)

    El-Fadaly, H.; El-Defrawy, M.M.; El-Zawawy, F.; Makia, D.

    1999-01-01

    The chemical analysis included quantitative measurement of electrical conductivity, alkalinity , hardness sulphate, ph, total dissolved solids, chloride, as well as dissolved oxygen was carried out. The microbiological examination for different water sources and industrial wastewater samples was also conducted. some of heavy metals, Co 2+ Cu 2+ Fe 3+ and Mn 2+ were determined in fresh water, while other metals, such as Cr 6+ , Co 2+ , Zn 2+ and Ni 2+ were measured in industrial wastewater. Results of the chemical analysis showed that all measured parameters were found within the limitation either national or international law, except some samples which showed higher values than the permissible limits for some measured parameters. The microbiological analysis exhibited presence of yeasts, fungi and bacteria. Most bacterial isolates were short rod, spore formers as well as coccoid shaped bacteria. The efficiency of water treatment process on the reduction of microbial load was also calculated. Regarding the pathogenic bacteria, data showed that neither water samples nor industrial wastewater contain pathogens when using specific cultivation media for the examination. Furthermore, data proved the possibility of recycling of the tested industrial wastewater on which some microorganisms can grow. Data showed that the percent of heavy metals removal can reach to more than 70% in some cases as a result to bacterial treatment of industrial wastewater

  3. Spectrophotometric determination of mercury in water samples after preconcentration using dispersive liquid-liquid microextraction.

    Science.gov (United States)

    Lemos, Valfredo Azevedo; dos Santos, Liz Oliveira; Silva, Eldevan dos Santos; Vieira, Emanuel Vitor dos Santos

    2012-01-01

    A simple method for the determination of mercury in water samples after preconcentration using dispersive liquid-liquid microextraction is described. The procedure is based on the extraction of mercury in the form of a complex and its subsequent determination by spectrophotometry. The complex is formed between Hg(II) and 2-(2-benzothiazolylazo)-p-cresol. The detection at 650 nm is performed directly in the metal-rich phase, which is spread on a triacetylcellulose membrane. The method eliminates the need to use a cuvet or large quantities of samples and reagents. The parameters that influence the preconcentration were studied, and the analytical characteristics were determined. The enrichment factor and the consumptive index for this method were 64 and 0.16 mL, respectively. The LOD (3.3 microg/L) and LOQ (11.1 microg/L) were also determined. The accuracy of the method was tested by the determination of mercury in certified reference materials BCR 397 (Human Hair) and SRM 2781 (Domestic Sludge). The method was applied to the determination of mercury in samples of drinking water, sea water, and river water.

  4. Radon Concentration And Dose Assessment In Well Water Samples From Karbala Governorate Of Iraq

    Science.gov (United States)

    Al-Alawy, I. T.; Hasan, A. A.

    2018-05-01

    There are numerous studies around the world about radon concentrations and their risks to the health of human beings. One of the most important social characteristics is the use of water wells for irrigation, which is a major source of water pollution with radon gas. In the present study, six well water samples have been collected from different locations in Karbala governorate to investigate radon concentration level using CR-39 technique. The maximum value 4.112±2.0Bq/L was in Al-Hurr (Al-Qarih Al-Easariah) region, and the lowest concentration of radon was in Hay Ramadan region which is 2.156±1.4Bq/L, with an average value 2.84±1.65Bq/L. The highest result of annual effective dose (AED) was in Al-Hurr (Al-Qarih Al-Easariah) region which is equal to 15.00±3.9μSv/y, while the minimum was recorded in Hay Ramadan 7.86±2.8μSv/y, with an average value 10.35±3.1μSv/y. The current results have shown that the radon concentrations in well water samples are lower than the recommended limit 11.1Bq/L and the annual effective dose in these samples are lower than the permissible international limit 1mSv/y.

  5. Direct sampling of chemical weapons in water by photoionization mass spectrometry.

    Science.gov (United States)

    Syage, Jack A; Cai, Sheng-Suan; Li, Jianwei; Evans, Matthew D

    2006-05-01

    The vulnerability of water supplies to toxic contamination calls for fast and effective means for screening water samples for multiple threats. We describe the use of photoionization (PI) mass spectrometry (MS) for high-speed, high-throughput screening and molecular identification of chemical weapons (CW) threats and other hazardous compounds. The screening technology can detect a wide range of compounds at subacute concentrations with no sample preparation and a sampling cycle time of approximately 45 s. The technology was tested with CW agents VX, GA, GB, GD, GF, HD, HN1, and HN3, in addition to riot agents and precursors. All are sensitively detected and give simple PI mass spectra dominated by the parent ion. The target application of the PI MS method is as a routine, real-time early warning system for CW agents and other hazardous compounds in air and in water. In this work, we also present comprehensive measurements for water analysis and report on the system detection limits, linearity, quantitation accuracy, and false positive (FP) and false negative rates for concentrations at subacute levels. The latter data are presented in the form of receiver operating characteristic curves of the form of detection probability P(D) versus FP probability P(FP). These measurements were made using the CW surrogate compounds, DMMP, DEMP, DEEP, and DIMP. Method detection limits (3sigma) obtained using a capillary injection method yielded 1, 6, 3, and 2 ng/mL, respectively. These results were obtained using 1-microL injections of water samples without any preparation, corresponding to mass detection limits of 1, 6, 3, and 2 pg, respectively. The linear range was about 3-4 decades and the dynamic range about 4-5 decades. The relative standard deviations were generally <10% at CW subacute concentrations levels.

  6. Sampling problems and the determination of mercury in surface water, seawater, and air

    International Nuclear Information System (INIS)

    Das, H.A.; van der Sloot, H.A.

    1976-01-01

    Analysis of surface water for mercury comprises the determination of both ionic and organically bound mercury in solution and that of the total mercury content of the suspended matter. Eventually, metallic mercury has to be determined too. Requirements for the sampling procedure are given. A method for the routine determination of mercury in surface water and seawater was developed and applied to Dutch surface waters. The total sample volume is 2500 ml. About 500 ml is used for the determination of the content of suspended matter and the total amount of mercury in the water. The sample is filtered through a bed of previously purified active charcoal at a low flow-rate. The main portion ca. 2000 ml) passes a flow-through centrifuge to separate the solid fraction. One liter is used to separate ''inorganic'' mercury by reduction, volatilization in an airstream and adsorption on active charcoal. The other liter is led through a column of active charcoal to collect all mercury. The procedures were checked with 197 Hg radiotracer both as an ion and incorporated in organic compounds. The mercury is determined by thermal neutron activation, followed by volatilization in a tube furnace and adsorption on a fresh carbon bed. The limit of determination is approximately equal to 1 ng 1 -1 . The rate of desorption from and adsorption on suspended material has been measured as a function of a pH of the solution for Hg +2 and various other ions. It can be concluded that only the procedure mentioned above does not disturb the equilibrium. The separation of mercury from air is obtained by suction of 1 m 3 through a 0.22 μm filter and a charcoal bed. The determination is then performed as in the case of the water samples

  7. Studies on radon concentration in underground water samples in and around Kabini river basin

    International Nuclear Information System (INIS)

    Yashaswini, T.; Ningappa, C.; Niranjan, R.S.; Sannappa, J.

    2017-01-01

    Radon is a radioactive inert gas, a decay product of radium, causes environmental health problems like lung cancer. Radium present in the earth crest continuously releases radon into underground water. From the point view of health, the study of radon concentration level in underground water base line data is important. In the present study, radon concentration in underground water have been measured in 40 underground water samples collected in and around Kabini River of Karnataka State by using Emanometry technique. The radon concentration in the study area varies from 21.2 to 168.2Bq.l -1 with a geometrical mean value of 73.3 Bq.l -1 . The physicochemical parameters of water such as chloride, Fluoride, nitrite, sulphate, TDS are measured in the same samples in order to know about the impact of these parameters on radon concentration and their health risks to the general public. The experimental techniques and results obtained are discussed in the presentation. (author)

  8. Lead in drinking water: sampling in primary schools and preschools in south central Kansas.

    Science.gov (United States)

    Massey, Anne R; Steele, Janet E

    2012-03-01

    Studies in Philadelphia, New York City, Houston, Washington, DC, and Greenville, North Carolina, have revealed high lead levels in drinking water. Unlike urban areas, lead levels in drinking water in suburban and rural areas have not been adequately studied. In the study described in this article, drinking water in primary schools and preschools in five suburban and rural south central Kansas towns was sampled to determine if any exceeded the U.S. Environmental Protection Agency (U.S. EPA) guidance level for schools and child care facilities of 20 parts per billion (ppb). The results showed a total of 32.1% of the samples had detectable lead levels and 3.6% exceeded the U.S. EPA guidance level for schools and child care providers of 20 ppb. These results indicate that about one-third of the drinking water consumed by children age six and under in the five suburban and rural south central Kansas towns studied has some lead contamination, exposing these children to both short-term and long-term health risks. The authors suggest a need for increased surveillance of children's drinking water in these facilities.

  9. Tritium Activity Measurement of Water Samples Using Liquid Scintillation Counter and Electrolytical Enrichment

    International Nuclear Information System (INIS)

    Baresic, J.; Krajcar Bronic, I.; Horvatincic, N.; Obelic, B.; Sironic, A.; Kozar-Logar J.

    2011-01-01

    Tritium (3H) activity of natural waters (precipitation, groundwater, surface waters) has recently become too low to be directly measured by low-level liquid scintillation (LSC) techniques. It is therefore necessary to perform electrolytical enrichment of tritium in such waters prior to LSC measurements. Electrolytical enrichment procedure has been implemented at the Rudjer Boskovic Institute (RBI) Tritium Laboratory in 2008, and since then 19 electrolyses have been completed. The mean enrichment factor E (a ratio between the final and initial 3H activities) after stabilisation of the system is E R BI = 22.5 @ 0.5, and the mean enrichment parameter (which describes the process of water mass reduction during electrolysis) is P R BI 0.949 @ 0.003. These values are comparable with those obtained at the Jo@ef Stefan Institute (JSI) Laboratory for liquid scintillation counting, at the electrolysis equipment of the same producer (AGH University of Science and Technology, Krakow, Poland) after 66 electrolyses carried out under identical conditions since 2007: E J SI = 18.9 @ 1.5, and P J SI = 0.896 @ 0.021. Both RBI and JSI laboratories have Ultra-low-level LSC Quantulus 1220 (Wallac, PerkinElmer) for measurement of 3H activity. A set of water samples having 3H activities in the range from 0 TU (''dead-water'' samples) to 18 000 TU (1 TU 0.118 Bq/L) were measured at both laboratories. Samples having 3H activity <200 TU were electrolytically enriched, while the others were measured directly in LSC. A very good agreement was obtained (correlation coefficient 0.991). Both laboratories participated in the IAEA TRIC2008 international intercomparison exercise. The analyses of reported 3H activity results in terms of z and u parameters showed that all results in both laboratories were acceptable. (author)

  10. A rapid and simple separation method of Tc-99 in water samples

    International Nuclear Information System (INIS)

    Uchida, Shigeo; Tagami, Keiko

    1999-01-01

    Technetium-99 ( 99 Tc) is one of the important elements on safety evaluation of reprocessing plant and waste disposal plant, because it is a long half-life nuclide and large fission yield (about 6%) from 235 U and 239 Pu. We studied in this work a rapid and simple separation method of 99 Tc in water samples by ICP-MS. Tc in 2 litre of inland water or 1.5 litre of sea water sample solutions was condensed and separated by mini-column resin (TEVA·Spec resin) (Eichrom Co., Ltd.). The experimental results showed the best conditions as followed that 1) after controlling 0.1M nitric acid sample solution, passed it through the column, 2) then the inhibitory elements such as Ru are removed by 40 ml of 2M nitric acid solution, and 3) Tc was recovered by 4 ml of 8M nitric acid solution. 95% or more recovery of Tc was obtained. 100% Ru, an inhibited element of ICP-MS, was removed. The elute obtained from 4 ml of 8M nitric acid solution was diluted ten times with pure water and 99 Tc was measured by ICP-MS. The limit of detection of 2 litre inland water and 1.5 litre sea water were 3 mBql -1 and 4 mBql -1 , respectively. The organic compounds were not removed before running to column, because the concentration of organic compounds was not so large. When large amounts of them are contained, they should be removed. If suspended materials absorb Tc, Tc should be changed to TcO 4 - . (S.Y.)

  11. Comparison of marine sampling methods for organic contaminants: Passive samplers, water extractions, and live oyster deployment.

    Science.gov (United States)

    Raub, Kristin B; Vlahos, Penny; Whitney, Michael

    2015-08-01

    Laboratory and field trials evaluated the efficacy of three methods of detecting aquatic pesticide concentrations. Currently used pesticides: atrazine, metolachlor, and diazinon and legacy pesticide dieldrin were targeted. Pesticides were extracted using solid-phase extraction (SPE) of water samples, titanium plate passive samplers coated in ethylene vinyl acetate (EVA) and eastern oysters (Crassostrea viginica) as biosamplers. A laboratory study assessed the extraction efficiencies and precision of each method. Passive samplers yielded the highest precision of the three methods (RSD: 3-14% EVA plates; 19-60% oysters; and 25-56% water samples). Equilibrium partition coefficients were derived. A significant relationship was found between the concentration in oyster tissue and the ambient aquatic concentration. In the field (Housatonic River, CT (U.S.)) water sampling (n = 5) detected atrazine at 1.61-7.31 μg L(-1), oyster sampling (n = 2×15) detected dieldrin at n.d.-0.096 μg L(-1) SW and the passive samplers (n = 5×3) detected atrazine at 0.97-3.78 μg L(-1) SW and dieldrin at n.d.-0.68 μg L(-1) SW. Copyright © 2015 Elsevier Ltd. All rights reserved.

  12. Radiation hazard indices of soil and water samples in Northern Malaysian Peninsula.

    Science.gov (United States)

    Almayahi, B A; Tajuddin, A A; Jaafar, M S

    2012-11-01

    The radioactivity quantity and quality were determined in soil and water samples in Northern Malaysian Peninsula (NMP) using HPGe spectroscopy and GR-135 spectrometer. The (226)Ra, (232)Th and (40)K concentrations in soil samples are 57±2, 68±4 and 427±17 Bq kg(-1), respectively, whereas in water samples were found to be 2.86±0.79, 3.78±1.73 and 152±12 Bq l(-1), respectively. These concentrations are within those reported from literature in other countries in the world. The radiological hazard indices of the samples were also calculated. The mean values obtained from soil samples are 186 Bq kg(-1), 88 nGy h(-1), 108 μSv y(-1), 0.50 and 0.65 for Radium Equivalent Activity (Ra(eq)), Absorbed Dose Rates (D(R)), Annual Effective Dose Rates (ED), External Hazard Index (H(ex)) and Internal Hazard Index (H(in)) respectively, whereas, for water samples were found to be 20, 10, 13, 0.05 and 0.06, respectively. All the health hazard indices are well below their recommended limits, except in two soil sampling sites which were found to be (*)025 (1.1 H(ex)) and (*)026 (1.1 H(ex), 1.6 H(in)). The calculated and the measured gamma dose rates had a good correlation coefficient, R=0.88. Moreover, the average value radon is 20 (in the range of 7-64) Bq m(-3), a positive correlation (R=0.81) was observed between the (222)Rn and (226)Ra concentrations in samples measured by the SNC continuous radon monitor (model 1029, Sun Nuclear Corporation) and HPGe detector, respectively. Some soils in this study with H(in) and H(ex)samples, therefore, water after processing and filtration is safe and suitable for use in household and industrial purposes. Copyright © 2012 Elsevier Ltd. All rights reserved.

  13. Stable isotope characterization of pan-derived and directly sampled atmospheric water vapour

    International Nuclear Information System (INIS)

    Maric, R.; St. Amour, N.A.; Gibson, J.J.; Edwards, T.W.D.

    2002-01-01

    Isotopic characterization of atmospheric water vapour, δ A , and its temporal variability are important prerequisites for quantifying water balance of surface reservoirs and partitioning of evaporation and transpiration fluxes using isotope techniques. Here we present results from a detailed comparison of several methods for determining δ A in field situations, (i) by back-calculation from isotopic and micrometeorological monitoring of a steady-state terminal reservoir (standard Class-A evaporation pan) using boundary-layer mass transfer models [1], (ii) through direct (cryogenic) sampling of ambient atmospheric moisture, and (iii) using the precipitation-equilibrium approximation (i.e., δ A =δ P - ε*)

  14. Procedures for the collection and preservation of groundwater and surface water samples and for the installation of monitoring wells

    International Nuclear Information System (INIS)

    Korte, N.; Kearl, P.

    1984-01-01

    Proper sampling procedures are essential for a successful water-quality monitoring program. It must be emphasized, however, that it is impossible to maintain absolutely in-situ conditions when collecting and preserving a water sample, whether from a flowing stream or an aquifer. Consequently, the most that can reasonably be expected is to collect a best possible sample with minimal disturbance. This document describes procedures for installing monitoring wells and for collecting samples of surface water and groundwater. The discussion of monitoring wells includes mention of multilevel sampling and a general overview of vadose-zone monitoring. Guidelines for well installation are presented in detail. The discussion of water-sample collection contains evaluations of sampling pumps, filtration equipment, and sample containers. Sample-preservation techniques, as published by several government and private sources, are reviewed. Finally, step-by-step procedures for collection of water samples are provided; these procedures address such considerations as necessary equipment, field operations, and written documentation. Separate procedures are also included for the collection of samples for determination of sulfide and for reactive aluminum. The report concludes with a brief discussion of adverse sampling, conditions that may significantly affect the quality of the data. Appendix A presents a rationale for the development and use of statistical considerations in water sampling to ensure a more complete water quality monitoring program. 51 references, 9 figures, 4 tables

  15. Efficient sample preparation method based on solvent-assisted dispersive solid-phase extraction for the trace detection of butachlor in urine and waste water samples.

    Science.gov (United States)

    Aladaghlo, Zolfaghar; Fakhari, Alireza; Behbahani, Mohammad

    2016-10-01

    In this work, an efficient sample preparation method termed solvent-assisted dispersive solid-phase extraction was applied. The used sample preparation method was based on the dispersion of the sorbent (benzophenone) into the aqueous sample to maximize the interaction surface. In this approach, the dispersion of the sorbent at a very low milligram level was achieved by inserting a solution of the sorbent and disperser solvent into the aqueous sample. The cloudy solution created from the dispersion of the sorbent in the bulk aqueous sample. After pre-concentration of the butachlor, the cloudy solution was centrifuged and butachlor in the sediment phase dissolved in ethanol and determined by gas chromatography with flame ionization detection. Under the optimized conditions (solution pH = 7.0, sorbent: benzophenone, 2%, disperser solvent: ethanol, 500 μL, centrifuged at 4000 rpm for 3 min), the method detection limit for butachlor was 2, 3 and 3 μg/L for distilled water, waste water, and urine sample, respectively. Furthermore, the preconcentration factor was 198.8, 175.0, and 174.2 in distilled water, waste water, and urine sample, respectively. Solvent-assisted dispersive solid-phase extraction was successfully used for the trace monitoring of butachlor in urine and waste water samples. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. The Behavior of Corrosion Products in Sampling Systems under Boiling Water Reactor Conditions

    Energy Technology Data Exchange (ETDEWEB)

    Hermansson, Hans-Peter

    1977-08-15

    A high pressure loop has been used to simulate sampling systems employed under BWR conditions. The reliability of the sampling method was studied in a series of six test runs. A variety of parameters that are thought to influence the reliability of the sampling was investigated. These included piping geometry, water oxygen content, flow, temperature and temperature gradients. Amongst other things the results indicate that the loss by deposition of iron containing corrosion products does not exceed 50 %; this figure is only influenced to a minor extent by the above mentioned parameters. The major part of the corrosion products thus deposited is found along the first few meters of the piping and cooler coil. A moderate prolongation of a pipe which is already relatively long should thus be incapable of producing a major influence on the sampling error

  17. Sample preparation of waste water to determine metallic contaminants by X-ray fluorescence spectroscopy

    International Nuclear Information System (INIS)

    Gonzalez Olivos, Javier.

    1987-01-01

    Trace X-ray fluorescence spectroscopy analysis in liquid samples is preceded by sample preparation, which usually consists in the precipitation of the metallic ions and concentration over a thin cellulose filter. The samples preparation of waste water by this method is not efficient, due to the great amount of organic and insoluble matter that they contain. The purpose of this work was to determine the optimal value of pH in order to adsorbe all the insoluble matter contained in a waste water sample in the activated charcoal, so that the metallic ions could be precipitated and concentrated on a thin filter and determinated by X-ray fluorescence spectroscopy. A survey about the adsorption of some ions in activated charcoal in function of the pH was made for the following: Cr 3+ , Fe 3+ , Ni 2+ , Cu 2+ , Zn 2+ , Se 2+ , Hg 2+ , and Pb 2+ . It was observed that at pH 0, the ions are not adsorbed, but Cu 2+ and Zn 2+ are adsorbed in small amount; at pH 14, the ions are adsorbed, excluding Se, which is not adsorbed at any value of pH. If a waste water sample is treated at pH 0 with activated charcoal to adsorbe the organic and insoluble matter, most of the metallic ions are not adsorbed by the activated charcoal and could be precipitated with APDC (ammonium 1-pirrolidine dithio carbamate salt) and concentrated on a thin filter. The analysis of the metallic ions contained on the filter and those adsorbed in the activated charcoal by X-ray fluorescence spectroscopy, gave the total amount of the ions in the sample. (author)

  18. Sampling tritiated water vapor from the atmosphere by an active system using silica gel

    Energy Technology Data Exchange (ETDEWEB)

    Herranz, M. [Department of Nuclear Engineering and Fluid Mechanics, E.T.S.I. de Bilbao, University of the Basque Country (UPV/EHU), Alameda de Urquijo, s/n 48013 Bilbao (Spain); Alegria, N., E-mail: natalia.alegria@ehu.es [Department of Nuclear Engineering and Fluid Mechanics, E.T.S.I. de Bilbao, University of the Basque Country (UPV/EHU), Alameda de Urquijo, s/n 48013 Bilbao (Spain); Idoeta, R.; Legarda, F. [Department of Nuclear Engineering and Fluid Mechanics, E.T.S.I. de Bilbao, University of the Basque Country (UPV/EHU), Alameda de Urquijo, s/n 48013 Bilbao (Spain)

    2011-11-15

    Among the different methods used to collect the tritiated water vapor (HTO) contained in the atmosphere, one of the most worldwide used is its collection using an air pump, which forces the air to pass through a dry silica gel trap. The silica gel is then distilled to remove the water collected, which is measured in a liquid scintillation counting system. In this paper, an analysis of the water collection efficiency of the silica gel has been done as a function of the temperatures involved, the dimensions of the pipe driving the air into the silica gel traps, the air volume passing through the trap and the flow rates used. Among the obtained conclusions, it can be pointed out that placing the traps inside a cooled container, the amount of silica gel needed to collect all the water contained in the air passing through these traps can be estimated using a weather forecast and a psychometric chart. To do this, and as thermal equilibrium between incoming and open air should be established, a suitable design of the sampling system is proposed. - Highlights: > To recollect the atmosphere air tritiated water vapor, an active system was used. > The system is an air pump and three traps with silica gel connected by a rubber pipe. > The silica gel retention depends on the meteorological conditions and the flow rate. > The amount of water collected and the mass of silica gel need were calculated, F.

  19. Analysis of Heavy Metals in Water and Fish (Tilapia sp.) Samples from Tasik Mutiara, Puchong

    International Nuclear Information System (INIS)

    Ismaniza Ismail; Idaliza Mat Saleh

    2012-01-01

    The concentrations of seven heavy metals (Al, As, Cd, Cu, Fe, Pb and Zn) were detected in muscle tissues of Tilapia sp. (black tilapia) collected from the lake of Taman Mutiara, Puchong. Samples were collected for several months in the end of 2009 at three sampling points. Heavy metals in fish and water samples were analyzed by Inductively Coupled Plasma - Optical Emission Spectroscopy (ICP-OES). Only Al, Cu, Fe and Zn were detected in the order Fe > Zn > Al > Cu, whereas concentrations of As, Cd and Pb were below the detection limit. The concentrations of heavy metals in water samples were low and below the detection limit. The levels of heavy metals in the fish samples can be considered as a serious matter of concern as it may be consumed and it signifies the degradation of lake quality. Generally, the sources of heavy metals in the Tasik Mutiara, Puchong could be attributed to the illegal waste dumping activity and discharge from the nearby sewage treatment plant into the lake which promote eutrophication in the lake. It could also be attributed to the Low Dissolved Oxygen (DO) levels in the lake. (author)

  20. UMTRA ground water sampling techniques: Comparison of the traditional and low flow methods

    International Nuclear Information System (INIS)

    1995-07-01

    This report describes the potential changes in water quality data that may occur with the conversion from MBV (multiple bore volume) to LF (low flow) sampling and provides two examples of how such a change might impact Project decisions. The existing scientific literature on LF sampling is reviewed and the new LF data from three UMTRA Uranium Mill Tailings Remedial Action Project sites are evaluated seeking answers to the questions posed above. Several possible approaches, that the UMTRA Project may take to address issues unanswered by the literature are presented and compared, and a recommendation is offered for the future direction of the LF conversion effort

  1. Application of enzyme multibiosensor for toxicity analysis of real water samples of different origin

    Directory of Open Access Journals (Sweden)

    Soldatkin A. P.

    2009-06-01

    Full Text Available Aim. The analysis of toxicity of different water samples with the multibiosensor developed earlier. Methods. The potentiometric multibiosensor with several immobilized enzymes as bioselective elements and the matrix of pH-sensitive field effect transistors as transducers of the biochemical signal into the electric one was applied for the analysis. Results. The bioselective elements of the multibiosensor were developed using acetylcholinesterase, butyryl- cholinesterase, urease, glucose oxidase, and three-enzyme system (invertase, mutarotase, glucose oxidase. The measurement of toxic compounds in water samples of different origin was performed using the constructed sensor. The results obtained were compared with those obtained by the conventional methods of toxic agent’s analysis (atomic absorption spectrometry, thin-film chroma- tography, and atomic absorbic analyser of mercury. Conclusion. A strong conformity between the results obtained with the multibiosensor and traditional methods has been shown.

  2. Statistical Methods and Sampling Design for Estimating Step Trends in Surface-Water Quality

    Science.gov (United States)

    Hirsch, Robert M.

    1988-01-01

    This paper addresses two components of the problem of estimating the magnitude of step trends in surface water quality. The first is finding a robust estimator appropriate to the data characteristics expected in water-quality time series. The J. L. Hodges-E. L. Lehmann class of estimators is found to be robust in comparison to other nonparametric and moment-based estimators. A seasonal Hodges-Lehmann estimator is developed and shown to have desirable properties. Second, the effectiveness of various sampling strategies is examined using Monte Carlo simulation coupled with application of this estimator. The simulation is based on a large set of total phosphorus data from the Potomac River. To assure that the simulated records have realistic properties, the data are modeled in a multiplicative fashion incorporating flow, hysteresis, seasonal, and noise components. The results demonstrate the importance of balancing the length of the two sampling periods and balancing the number of data values between the two periods.

  3. Rapid determination of phenolic compounds in water samples by alternating-current oscillopolarographic titration

    Institute of Scientific and Technical Information of China (English)

    XIAO Jun-ping; WANG Xue-feng; ZHOU Qing-xiang; FAN Xiao-yuan; SU Xian-fa; Bai Hua-hua; DUAN Hai-jing

    2007-01-01

    A rapid, simple and sensitive method was demonstrated for the determination of phenolic compounds in water samples by alternating-current oscillopolarographic titration. With the presence of sulfuric acid, phenol could be transferred into a nitroso-compound by reacting with NaNO2. The titration end-point was obtained by the formation of a sharp cut in the oscillopolarographic with infinitesimal NaNO2 on double platinum electrodes. The results showed that phenol had an excellent linear relationship over the range of 4.82×10-6 -9.65×10-3 mol/L, the RSD of the proposed method was lower than 1.5%, and the spiked recoveries of three real water samples were in the range of 95.6%-106.9%.

  4. Laser Spectroscopic Analysis of Liquid Water Samples for Stable Hydrogen and Oxygen Isotopes

    International Nuclear Information System (INIS)

    2009-01-01

    Stable isotope ratios of hydrogen and oxygen are tracers of choice for water cycle processes in hydrological, atmospheric and ecological studies. The use of isotopes has been limited to some extent because of the relatively high cost of isotope ratio mass spectrometers and the need for specialized operational skills. Here, the results of performance testing of a recently developed laser spectroscopic instrument for measuring stable hydrogen and oxygen isotope ratios of water samples are described, along with a procedure for instrument installation and operation. Over the last four years, the IAEA Water Resources Programme conducted prototype and production model testing of these instruments and this publication is the outcome of those efforts. One of the main missions of the IAEA is to promote the use of peaceful applications of isotope and nuclear methods in Member States and this publication is intended to facilitate the use of laser absorption based instruments for hydrogen and oxygen stable isotope analyses of liquid water samples for hydrological and other studies. The instrument uses off-axis integrated cavity output spectroscopy to measure absolute abundances of 2 HHO, HH 18 O, and HHO via laser absorption. Test results using a number of natural and synthetic water standards and samples with a large range of isotope values demonstrate adequate precision and accuracy (e.g. precisions of 1 per mille for δ 2 H and 0.2 per mille for δ 18 O). The laser instrument has much lower initial and maintenance costs than mass spectrometers and is substantially easier to operate. Thus, these instruments have the potential to bring about a paradigm shift in isotope applications by enabling researchers in all fields to measure isotope ratios by themselves. The appendix contains a detailed procedure for the installation and operation of the instrument. Using the procedure, new users should be able to install the instrument in less than two hours. It also provides step

  5. Iodide-assisted total lead measurement and determination of different lead fractions in drinking water samples.

    Science.gov (United States)

    Zhang, Yuanyuan; Ng, Ding-Quan; Lin, Yi-Pin

    2012-07-01

    Lead and its compounds are toxic and can harm human health, especially the intelligence development in children. Accurate measurement of total lead present in drinking water is crucial in determining the extent of lead contamination and human exposure due to drinking water consumption. The USEPA method for total lead measurement (no. 200.8) is often used to analyze lead levels in drinking water. However, in the presence of high concentration of the tetravalent lead corrosion product PbO(2), the USEPA method was not able to fully recover particulate lead due to incomplete dissolution of PbO(2) particles during strong acid digestion. In this study, a new procedure that integrates membrane separation, iodometric PbO(2) measurement, strong acid digestion and ICP-MS measurement was proposed and evaluated for accurate total lead measurement and quantification of different lead fractions including soluble Pb(2+), particulate Pb(II) carbonate and PbO(2) in drinking water samples. The proposed procedure was evaluated using drinking water reconstituted with spiked Pb(2+), spiked particulate Pb(II) carbonate and in situ formed or spiked PbO(2). Recovery tests showed that the proposed procedure and the USEPA method can achieve 93-112% and 86-103% recoveries respectively for samples containing low PbO(2) concentrations (0.018-0.076 mg Pb per L). For samples containing higher concentrations of PbO(2) (0.089-1.316 mg Pb per L), the USEPA method failed to meet the recovery requirement for total lead (85-115%) while the proposed method can achieve satisfactory recoveries (91-111%) and differentiate the soluble Pb(2+), particulate Pb(II) carbonate and PbO(2).

  6. Derivative activation analysis of phosphorus at ppb levels in water samples

    International Nuclear Information System (INIS)

    Arunachalam, J.; John, A.; Gangadharan, S.

    1991-01-01

    A neutron activation analysis procedure has been developed for the indirect determination of phosphorus as orthophosphate at ppb levels, via the formation of antimonyl phosphomolybdic acid. The complex is adsorbed on Sephadex G-25 resin and the antimony is estimated through NAA, allowing the determination of phosphorus. The procedure provides an easy method to adopt for the routine determination of phosphorus at ≥ 10 ng ml -1 levels with good precision, in water samples. (author) 6 refs.; 5 tabs

  7. Genome Sequence of Legionella massiliensis, Isolated from a Cooling Tower Water Sample.

    Science.gov (United States)

    Pagnier, Isabelle; Croce, Olivier; Robert, Catherine; Raoult, Didier; La Scola, Bernard

    2014-10-16

    We present the draft genome sequence of Legionella massiliensis strain LegA(T), recovered from a cooling tower water sample, using an amoebal coculture procedure. The strain described here is composed of 4,387,007 bp, with a G+C content of 41.19%, and its genome has 3,767 protein-coding genes and 60 predicted RNA genes. Copyright © 2014 Pagnier et al.

  8. Sampling system of atmospheric water vapour for analysis of the γ sub(D) relationship

    International Nuclear Information System (INIS)

    Foloni, L.L.; Villa Nova, N.A.; Salati, E.

    1979-01-01

    The development of a system to water vapour air, for natural isotopic composition analysis of hydrogen is presented. The system uses molecular sieve, type '4A', without cooling agent and permits the choice of a sampling time, variyng from a few minutes to many hours, through the control of the admission of vapour flux. The system has good performance in field conditions, with errors of the order of + -3,0 0 /00 in the γ sub(D)( 0 /00) measurements [pt

  9. UMTRA project water sampling and analysis plan, Old and New Rifle, Colorado

    International Nuclear Information System (INIS)

    1994-07-01

    Surface remedial action at the Rifle, Colorado, Uranium Mill Tailings Remedial Action (UMTRA) Project site began in the spring of 1992. Results of water sampling at the Old and New Rifle processing sites for recent years indicate that ground water contamination occurs in the shallow unconfined alluvial aquifer (the uppermost aquifer) and less extensively in the underlying Wasatch Formation. Uranium and sulfate continue to exceed background ground water concentrations and/or maximum concentration limits at and downgradient from the former processing sites. These constituents provide the best indication of changes in contaminant distribution. Contamination in the uppermost (alluvial) aquifer at New Rifle extends a minimum of approximately 5000 feet (ft) (1,524 meters [m]) downgradient. At Old Rifle, the extent of contamination in the alluvial aquifer is much less (a minimum of approximately 1,000 ft [305 m]), partially due to differences in hydrologic regime. For example, the Old Rifle site lies in a relatively narrow alluvial floodplain; the New Rifle site lies in a broad floodplain. Data gathering for the Rifle baseline risk assessment is under way. The purpose of this effort is to determine with greater precision the background ground water quality and extent of ground water contamination at the processing sites. Historical surface water quality indicates that the Colorado River has not been affected by uranium processing activities. No compliance monitoring of the Estes Gulch disposal cell has been proposed, because ground water in the underlying Wasatch Formation is limited use (Class 111) ground water and because the disposal cell is hydrogeologically isolated from the uppermost aquifer

  10. Sources of variability in the determination by evaporation method of gross alpha activity in water samples

    Energy Technology Data Exchange (ETDEWEB)

    Baeza, A.; Corbacho, J.A. [LARUEX, Caceres (Spain). Environmental Radioactivity Lab.

    2013-07-01

    Determining the gross alpha activity concentration of water samples is one way to screen for waters whose radionuclide content is so high that its consumption could imply surpassing the Total Indicative Dose as defined in European Directive 98/83/EC. One of the most commonly used methods to prepare the sources to measure gross alpha activity in water samples is desiccation. Its main advantages are the simplicity of the procedure, the low cost of source preparation, and the possibility of simultaneously determining the gross beta activity. The preparation of the source, the construction of the calibration curves, and the measurement procedure itself involve, however, various factors that may introduce sufficient variability into the results to significantly affect the screening process. We here identify the main sources of this variability, and propose specific procedures to follow in the desiccation process that will reduce the uncertainties, and ensure that the result is indeed representative of the sum of the activities of the alpha emitters present in the sample. (orig.)

  11. SPME GC/MS determination of organochlorine pesticides in water samples

    Directory of Open Access Journals (Sweden)

    Yerbolat Sailaukhanuly

    2013-05-01

    Full Text Available Headspace solid phase microextraction (HS-SPME in combination with gas chromatography and mass-spectrometry (GC/MS was studied for analysis of water samples. The organochlorine pesticides (OCPs, p,p'-DDT, p,p'-DDD, and p,p'-DDE were collected and analyzed by GC/MS. To select of effective fiber coatings four types of SPME fibers were examined and compared. The parameters effecting the efficiency of HS-SPME such as extraction and pre-incubation time and extraction temperature, effect of solvent nature, ionic strength were studied to obtain optimal parameters. The method was developed using spiked water samples in a concentration range  10 - 500 ng/L. The calibration curve was linear over the studied concentration range with r≥0.9925. The detection limits varied from 1.57 to 2.08 ng/L. An authentic water samples from contaminated lake with OCPs were analyzed by developed method.

  12. Measurement of the deuterium concentration in water samples using a CW chemical deuterium fluoride laser

    International Nuclear Information System (INIS)

    Trautmann, M.

    1979-10-01

    In this study a new method for the determination of the deuterium content in water samples is described. The absorption of the radiation of a CW deuterium fluoride laser by the isotope HDO in the water vapor of the sample is measured by means of an optoacoustic detector (spectrophone). Thereby advantage is taken of the fact that H 2 O hardly absorbs the laser radiation and that D 2 O only exists in negligible concentrations. The isotope ratio of hydrogen can be calculated from the measured relative concentration of HDO. In the course of this investigation the relative absorption cross sections of HDO for the different laser lines were determined. It was thereby established that there exists a very good coincidence of an HDO absorption line with the 2P2 laser line. Using a very sensitive nonresonant spectrophone the relative concentration of HDO in natural water samples could be determined with an accuracy of about 10%. The experiments also demonstrated that with appropriate improvements made to the apparatus and using a second spectrophone as a reference it should be possible to increase this accuracy to 0,1%. (orig.)

  13. Temperature dependence of the calibration factor of radon and radium determination in water samples by SSNTD

    CERN Document Server

    Hunyadi, I; Hakl, J; Baradacs, E; Dezso, Z

    1999-01-01

    The sensitivity of a sup 2 sup 2 sup 6 Ra determination method of water samples by SSNTD was measured as a function of storage temperature during exposure. The method is based on an etched track type radon monitor, which is closed into a gas permeable foil and is immersed in the water sample. The sample is sealed in a glass vessel and stored for an exposure time of 10-30 days. The sensitivity increased more than a factor of two when the storage temperature was raised from 2 deg. C to 30 deg. C. Temperature dependence of the partition coefficient of radon between water and air provides explanation for this dependence. For practical radio- analytical application the temperature dependence of the calibration factor is given by fitting the sensitivity data obtained by measuring sup 2 sup 2 sup 6 Ra standard solutions (in the activity concentration range of 0.1-48.5 kBq m sup - sup 3) at different storage temperatures.

  14. Pumping time required to obtain tube well water samples with aquifer characteristic radon concentrations

    International Nuclear Information System (INIS)

    Ricardo, Carla Pereira; Oliveira, Arno Heeren de

    2011-01-01

    Radon is an inert noble gas, which comes from the natural radioactive decay of uranium and thorium in soil, rock and water. Radon isotopes emanated from radium-bearing grains of a rock or soil are released into the pore space. Radon that reaches the pore space is partitioned between the gaseous and aqueous phases. Thus, the groundwater presents a radon signature from the rock that is characteristic of the aquifer. The characteristic radon concentration of an aquifer, which is mainly related to the emanation, is also influenced by the degree of subsurface degassing, especially in the vicinity of a tube well, where the radon concentration is strongly reduced. Looking for the required pumping time to take a tube well water sample that presents the characteristic radon concentration of the aquifer, an experiment was conducted in an 80 m deep tube well. In this experiment, after twenty-four hours without extraction, water samples were collected periodically, about ten minutes intervals, during two hours of pumping time. The radon concentrations of the samples were determined by using the RAD7 Electronic Radon Detector from Durridge Company, a solid state alpha spectrometric detector. It was realized that the necessary time to reach the maximum radon concentration, that means the characteristic radon concentration of the aquifer, is about sixty minutes. (author)

  15. Measurement of stable isotope ratio of organic carbon in water samples

    International Nuclear Information System (INIS)

    Fujii, Toshihiro; Otsuki, Akira

    1977-01-01

    A new method for the measurement of stable isotope ratios was investigated and applied to organic carbon's isotope ratio measurements in water samples. A few river water samples from Tsuchiura city were tested. After the wet oxidation of organic carbons to carbon dioxide in a sealed ampoule, the isotope ratios were determined with the gas chromatograph-quadrupole mass spectrometer combined with a total organic carbon analyser, under the dynamic conditions. The GC-MS had been equipped with the multiple ion detector-digital integrator system. The ion intensities at m/e 44 and 45 were simultaneously measured at a switching rate of 1 ms. The measurements with carbon dioxide acquired from sodium carbonate (53 μg) gave the isotope ratios with the variation coefficient of 0.62%. However, the variation coefficients obtained from organic carbons in natural water samples were 2 to 3 times as high as that from sodium carbonate. This method is simple and rapid and may be applied to various fields especially in biology and medicine. (auth.)

  16. Development of radiochemical methods for the determination of radionuclides in water samples

    International Nuclear Information System (INIS)

    Vajda, N.; Molnar, Zs.; Bodizs, D.

    2004-01-01

    are high, in the range of 10 -4 -10 -6 Bq/L. 90 Sr and Pu nuclides have been determined in the surveillance wells of the Hungarian nuclear power plant for several years. Ground level measurements have been performed in the area of the future radioactive waste disposal site. Radionuclides of natural origin have typically significantly higher concentrations than those of artificial nuclides, thus methods of moderate sensitivities have been developed/adopted for the determination of U and Th as well as Ra and Po isotopes. Uranium and thorium are separated in a combined procedure by extraction chromatography using an organic phosphonate compound. Ra and Po are consecutively separated from the same sample aliquot, Po is spontaneously deposited onto Ag disc, while from the supernate Ra is co-precipitated with Ba sulfate. Alpha spectrometry is used for the sensitive detection of 238 U, 235 U, 234 U, 232 Th, 230 Th, 228 Th, 210 Po and 226 Ra. Analyzing 100-1000 ml water samples detection limits in the range of 10 -2 -10 -4 Bq/L were obtained. The procedure has been successfully applied for ground level determination in tile area of the future radioactive waste disposal site in Hungary. To increase the accuracy of each method radioactive tracers or stable carriers were added to each sample/each analyte before chelnical processing and results were corrected for chemical losses. Methods were validated by measuring reference materials and performing proficiency tests. (authors)

  17. Sampling method of water sources at study site Taiping, Perak and Pulau Burung, Penang for research on pollutant movement in underground water

    International Nuclear Information System (INIS)

    Mohd Rifaie Mohd Murtadza; Mohd Tadza Abdul Rahman; Kamarudin Samuding; Roslanzairi Mostapa

    2005-01-01

    This paperwork explain the method of water sampling being used to take the water samples from the study sites in Taiping, Perak and Pulau Burung, Pulau Pinang. The sampling involve collecting of water samples for groundwater from boreholes and surface water from canal, river, pond, and ex-mining pond from several locations at the study sites. This study also elaborates the instruments and chemical used. The main purpose of this sampling are to obtain the important water quality parameters such as pH, conductivity, Total Dissolved Solid (TDS), heavy metals, anions, cations, and environmental isotopes delta values (d) for 18O, Deuterium dan Tritium. A correct sampling method according to standard is very important to ensure an accurate and precise results. With this, the data from the laboratory tests result can be fully utilized to make the interpretation of the pollutants movement. (Author)

  18. Detection of toxic compounds in real water samples using a conductometric tyrosinase biosensor

    International Nuclear Information System (INIS)

    Anh, Tuan Mai; Dzyadevych, Sergei V.; Prieur, Nicolas; Duc, Chien Nguyen; Pham, T.D.; Renault, Nicole Jaffrezic; Chovelon, Jean-Marc

    2006-01-01

    A conductometric tyrosinase biosensor for the detection of some toxic compounds including diuron, atrazine, and copper ions was developed. The work of this biosensor is based on the principle of change of conductivity of the enzyme membrane when tyrosinase either interacts with 4-chlorophenol substrate or is inhibited by pollutants. The different samples tested were solutions containing diuron, atrazine, copper, lead and zinc ions, mixtures of copper/atrazine or copper/diuron and real water samples coming from a Vietnamese river. In the last case, classical techniques such as GC-MS or atomic absorption spectrometry were used in order to estimate exact concentration of these species in real water samples. Results have shown that such a biosensor could be used as an early warning system for the detection of these pollutants, as no matrix effect coming from the real sample was observed and no synergetic or antagonist effects were found for the mixture of toxic compounds. In addition, results were coherent with the content of the tyrosinase inhibitors

  19. Detection of toxic compounds in real water samples using a conductometric tyrosinase biosensor

    Energy Technology Data Exchange (ETDEWEB)

    Anh, Tuan Mai [Laboratoire d' Application de la Chimie a l' Environnement, UMR CNRS 5634, Universite Claude Bernard Lyon I, 43 Boulevard du 11 Nov. 1918, 69622 Villeurbanne Cedex (France); International Training Institute for Materials Science (ITIMS), Hanoi University of Technology, 1 Dai Co Viet, Hanoi, Vietnam (Viet Nam); Dzyadevych, Sergei V. [Laboratory of Biomolecular Electronics, Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine, 150 Zabolotnogo Str., Kiev 03143 (Ukraine); Prieur, Nicolas [Institute of Natural Products Chemistry, Vietnam National Centre for Science and Technology, Hoang Quoc Viet Str., Hanoi, Vietnam (Viet Nam); Duc, Chien Nguyen [International Training Institute for Materials Science (ITIMS), Hanoi University of Technology, 1 Dai Co Viet, Hanoi, Vietnam (Viet Nam); Pham, T.D. [International Training Institute for Materials Science (ITIMS), Hanoi University of Technology, 1 Dai Co Viet, Hanoi, Vietnam (Viet Nam); Renault, Nicole Jaffrezic [Ecole Centrale de Lyon, CEGELY, UMR CNRS 5005, 36 Avenue Guy de Collongue, 69134 Ecully Cedex (France); Chovelon, Jean-Marc [Laboratoire d' Application de la Chimie a l' Environnement, UMR CNRS 5634, Universite Claude Bernard Lyon I, 43 Boulevard du 11 Nov. 1918, 69622 Villeurbanne Cedex (France)]. E-mail: chovelon@univ-lyon1.fr

    2006-03-15

    A conductometric tyrosinase biosensor for the detection of some toxic compounds including diuron, atrazine, and copper ions was developed. The work of this biosensor is based on the principle of change of conductivity of the enzyme membrane when tyrosinase either interacts with 4-chlorophenol substrate or is inhibited by pollutants. The different samples tested were solutions containing diuron, atrazine, copper, lead and zinc ions, mixtures of copper/atrazine or copper/diuron and real water samples coming from a Vietnamese river. In the last case, classical techniques such as GC-MS or atomic absorption spectrometry were used in order to estimate exact concentration of these species in real water samples. Results have shown that such a biosensor could be used as an early warning system for the detection of these pollutants, as no matrix effect coming from the real sample was observed and no synergetic or antagonist effects were found for the mixture of toxic compounds. In addition, results were coherent with the content of the tyrosinase inhibitors.

  20. Solid phase extraction for determination of 90Sr in water sample

    International Nuclear Information System (INIS)

    Ometakova, J.

    2009-01-01

    We studied the use of an extraction chromatography for determination of 90 Sr in samples of contaminated water. The aim of the thesis was to compare selected products from the point of view of the strontium yields and time needed. Three commercial products: 3M Empore Strontium Rad Disk, AnaLig, Sr-Resin and two classical methods: liquid-liquid extraction with tributylphosphate and carbonate co-precipitation (to eliminate interferers) were used for separation of 90 Sr. The water sample was used in radiochemical analysis for determination volume activity of 90 Sr. A radiochemical strontium yield was traced by using radionuclide 85 Sr. Samples were counted over a two week period to monitor the ingrowth of 90 Y on TRI CARB LSC counter. Samples were measured using an HPGe detector to find out 85 Sr recoveries at 514 keV line and they were counted directly by Cherenkov counting after the growth of 90 Y using TriCarb LSC counter after a two- week period (author)

  1. Pore water sampling in acid sulfate soils: a new peeper method.

    Science.gov (United States)

    Johnston, Scott G; Burton, Edward D; Keene, Annabelle F; Bush, Richard T; Sullivan, Leigh A; Isaacson, Lloyd

    2009-01-01

    This study describes the design, deployment, and application of a modified equilibration dialysis device (peeper) optimized for sampling pore waters in acid sulfate soils (ASS). The modified design overcomes the limitations of traditional-style peepers, when sampling firm ASS materials over relatively large depth intervals. The new peeper device uses removable, individual cells of 25 mL volume housed in a 1.5 m long rigid, high-density polyethylene rod. The rigid housing structure allows the device to be inserted directly into relatively firm soils without requiring a supporting frame. The use of removable cells eliminates the need for a large glove-box after peeper retrieval, thus simplifying physical handling. Removable cells are easily maintained in an inert atmosphere during sample processing and the 25-mL sample volume is sufficient for undertaking multiple analyses. A field evaluation of equilibration times indicates that 32 to 38 d of deployment was necessary. Overall, the modified method is simple and effective and well suited to acquisition and processing of redox-sensitive pore water profiles>1 m deep in acid sulfate soil or any other firm wetland soils.

  2. UMTRA project water sampling and analysis plan, Ambrosia Lake, New Mexico

    International Nuclear Information System (INIS)

    1994-02-01

    This water sampling and analysis plan (WSAP) provides the basis for ground water sampling at the Ambrosia Lake Uranium Mill Tailings Remedial Action (UMTRA) Project site during fiscal year 1994. It identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequency for the monitoring locations and will be updated annually. The Ambrosia Lake site is in McKinley County, New Mexico, about 40 kilometers (km) (25 miles [mi]) north of Grants, New Mexico, and 1.6 km (1 mi) east of New Mexico Highway 509 (Figure 1.1). The town closest to the tailings pile is San Mateo, about 16 km ( 10 mi) southeast (Figure 1.2). The former mill and tailings pile are in Section 28, and two holding ponds are in Section 33, Township 14 North, Range 9 West. The site is shown on the US Geological Survey (USGS) map (USGS, 1980). The site is approximately 2100 meters (m) (7000 feet [ft]) above sea level

  3. The measurement of tritium in water samples with electrolytic enrichment using liquid scintillation counter

    Directory of Open Access Journals (Sweden)

    Janković Marija M.

    2012-01-01

    Full Text Available Tritium (3H present in the environment decreased in the last decades and nowadays it has low activity concentrations. Measurement of low-level tritium activities in natural waters, e. g. in precipitation, groundwater, and river water requires special techniques for water pretreatment and detection of low-level radioactivity. In order to increase the tritium concentration to an easily measurable level, electrolytic enrichment must be applied. This paper presents the enrichment method performed by electrolysis in a battery of 18 cells, giving an enrichment factor of 5.84 (calculated from 59 electrolyses. The calculated mean values of the separation factor and enrichment parameter were 4.10 and 0.84, respectively. Results for tritium activity in precipitation and surface water collected in Belgrade during 2008 and 2009 are presented. The Radiation and Environmental Protection Department of the Vinča Institute of Nuclear Sciences, participated in the IAEA TRIC2008 international intercomparison exercise. The participation in the intercomparisons for any laboratory doing low-level 3H measurements in the waters is very important and useful. It is considered the best way to check the entire procedure and methods of the measurements and the reliability of the standard used. The analysis of the reported 3H activity results showed that all results for five intercomparison samples, for which electrolytic enrichment were applied prior to the 3H measurement, are acceptable.

  4. Cost-effective sampling of ground water monitoring wells. Revision 1

    International Nuclear Information System (INIS)

    Ridley, M.; Johnson, V.

    1995-11-01

    CS is a systematic methodology for estimating the lowest-frequency sampling schedule for a given groundwater monitoring location which will still provide needed information for regulatory and remedial decision-making. Increases in frequency dictated by remedial actions are left to the judgement of personnel reviewing the recommendations. To become more applicable throughout the life cycle of a ground water cleanup project or for compliance monitoring, several improvements are envisioned, including: chemical signature analysis to identify minimum suites of contaminants for a well, a simple flow and transport model so that sampling of downgradient wells are increased before movement of contamination, and a sampling cost estimation capability. By blending qualitative and quantitative approaches, we hope to create a defensible system while retaining interpretation ease and relevance to decision making

  5. Analytical procedures for determining Pb and Sr isotopic compositions in water samples by ID-TIMS

    Directory of Open Access Journals (Sweden)

    Veridiana Martins

    2008-01-01

    Full Text Available Few articles deal with lead and strontium isotopic analysis of water samples. The aim of this study was to define the chemical procedures for Pb and Sr isotopic analyses of groundwater samples from an urban sedimentary aquifer. Thirty lead and fourteen strontium isotopic analyses were performed to test different analytical procedures. Pb and Sr isotopic ratios as well as Sr concentration did not vary using different chemical procedures. However, the Pb concentrations were very dependent on the different procedures. Therefore, the choice of the best analytical procedure was based on the Pb results, which indicated a higher reproducibility from samples that had been filtered and acidified before the evaporation, had their residues totally dissolved, and were purified by ion chromatography using the Biorad® column. Our results showed no changes in Pb ratios with the storage time.

  6. Radium 226 and uranium isotopes simultaneously determination in water samples using liquid scintillation counter

    International Nuclear Information System (INIS)

    Al-Masri, M.S.; Al-Akel, B.; Saaid, S.; Nashawati, A.

    2007-04-01

    In this work a method has been developed to determine simultaneously Radium 226 and Uranium isotopes in water samples by low back ground Liquid Scintillation Counter. Radium 226 was determined by its progeny Polonium 214 after one month of sample storage in order to achieve the equilibrium between Radium 226 and Polonium 214. Uranium isotopes were determined by subtracting Radium 226 activity from total alpha activity. The method detection limits were 0.049 Bq/L and 0.176 Bq/L for Radium 226 and Uranium isotopes respectively. The repeatability limits were ± 0.32 Bq/L and ± 0.9 Bq/L for Radium 226 and Uranium isotopes respectively. While relative errors were % 9.5 and %18.2 for Radium 226 and Uranium isotopes respectively. On the other hand, the report presented the results of different standard and natural samples.(author)

  7. Flame Photometric Determination of Lithium Contents Down to 10{sup -3} ppm in Water Samples

    Energy Technology Data Exchange (ETDEWEB)

    Joensson, Guenther

    1963-04-15

    A flame photometric method has been developed for determination of submicro contents of lithium in water. The intensity of the emission from lithium increases about three times if 20 % of a mixture of acetone - amyl alcohol (4:1) is added to the sample. Interferences by stray light from sodium present is eliminated with a special absorption filter. Interferences from oxide bands of the alkaline earth metals are completely suppressed after adding aluminium to the sample. With the development of this routine method it is possible by flame photometry to directly determine 0.01 ppm lithium with an error of analysis less than 10 %. Furthermore the investigation shows that, after concentration of the sample by evaporation, contents down to 10{sup -3} ppm can be determined without any difficulty. One person can run up to 50 determinations per day.

  8. Establishing a routine procedure for extraction of water from vegetation samples

    International Nuclear Information System (INIS)

    Varlam, Carmen; Stefanescu, Ioan; Faurescu, Ionut; Vagner, Irina; Faurescu, Denisa

    2008-01-01

    Full text: The Cryogenic Pilot is an experimental project within the nuclear energy national research program, which has the aim of developing technologies for tritium and deuterium separation by cryogenic distillation. The process, used in this installation, is based on a combined method for liquid-phase catalytic exchange (LPCE) and cryogenic distillation. There are two ways that Cryogenic Pilot can interact with the environment: by atmospheric release and by sewage. In order to establish the base line of tritium concentration in the environment around the nuclear facilities we investigated the preparation procedure for different type of samples: soil, hay, apple, grass, milk, meat and water. For azeotropic distillation of all types of samples two solvents were used, toluene and cyclohexane, and all measurements for determination of environmental tritium concentration were carry out using liquid scintillation counting (LSC), with ultra-low level liquid scintillation spectrometer Quantulus 1220 specially designed for environmental samples and low radioactivity. Sample scintillation cocktail ratio was 8:12 ml and liquid scintillation cocktail was UltimaGold LLT. The background determined for control samples prepared ranged between 0.926 Cpm and 1.002 Cpm and counting efficiency between 25.3% and 26.1%. The counting time was 1000 minutes (50 minutes/20 cycles) for each sample, and minimum detectable activity according to ISO 9698 was 8.9 TU, and 9.05 TU, respectively, with a confidence coefficient of 3. (authors)

  9. Analysis and evaluation of compounds from Cichorium intybus aromatic water trade market samples

    Directory of Open Access Journals (Sweden)

    A. Hosseini*

    2017-11-01

    Full Text Available Background and objectives: Cichorium intybus products are one of the best sellers in market Because of their effect on treatment of infection, poisoning, diabetes and allergy. This is the first study about Cichorium intybus market samplephytochemical compounds and the aim of this study was to define a method to recognize the original products. Methods: The sample compounds were extracted by liquid-liquid method and evaluated by GC-MS and compared with the references like Adams 2007. The obtained phytochemical data were analyzed with SPSS and classified by dendrogram method and was compared with the data earned from the standard sample. Results: Forty one compounds were detected. Carvacrol was available in all samples from 1.14 to 39.34%. Also, thymol was present in most of samples from 1.24 to 69.32%. Moreover, we understood that some compounds like pulegone, carvone, carvacrol and piperitenone could be detected in all samples mostly with different percentages. Some linear hydrocarbon was detected in this method along with some other unexpected compounds like cinnamaldehyde. Conclusion: Existence of some impure compounds like: pulegone, carvone, piperitenone and cinnamaldehyde in trade samples showed cleaning of container might not have been proper. Carvacrol and thymol are common compounds to define acceptable standard for Cichorium intybus aromatic water.

  10. Water stable isotope measurements of Antarctic samples by means of IRMS and WS-CRDS techniques

    Science.gov (United States)

    Michelini, Marzia; Bonazza, Mattia; Braida, Martina; Flora, Onelio; Dreossi, Giuliano; Stenni, Barbara

    2010-05-01

    In the last years in the scientific community there has been an increasing interest for the application of stable isotope techniques to several environmental problems such as drinking water safeguarding, groundwater management, climate change, soils and paleoclimate studies etc. For example, the water stable isotopes, being natural tracers of the hydrological cycle, have been extensively used as tools to characterize regional aquifers and to reconstruct past temperature changes from polar ice cores. Here the need for improvements in analytical techniques: the high request for information calls for technologies that can offer a great quantity of analyses in short times and with low costs. Furthermore, sometimes it is difficult to obtain big amount of samples (as is the case for Antarctic ice cores or interstitial water) preventing the possibility to replicate the analyses. Here, we present oxygen and hydrogen measurements performed on water samples covering a big range of isotopic values (from very negative antarctic precipitation to mid-latitude precipitation values) carried out with both the conventional Isotope Ratio Mass Spectrometry (IRMS) technique and with a new method based on laser absorption techniques, the Wavelenght Scanned Cavity Ringdown Spectroscopy (WS-CRDS). This study is focusing on improving the precision of the measurements carried out with WS-CRDS in order to extensively apply this method to Antarctic ice core paleoclimate studies. The WS-CRDS is a variation of the CRDS developed in 1988 by O'Keef and Deacon. In CRDS a pulse of light goes through a box with high reflective inner surfaces; when there is no sample in the box the light beam doesn't find any obstacle in its path, but the reflectivity of the walls is not perfect so eventually there will be an absorption of the light beam; when the sample is injected in the box there is absorption and the difference between the time of absorption without and with sample is proportional to the quantity

  11. High-frequency, long-duration water sampling in acid mine drainage studies: a short review of current methods and recent advances in automated water samplers

    Science.gov (United States)

    Chapin, Thomas

    2015-01-01

    Hand-collected grab samples are the most common water sampling method but using grab sampling to monitor temporally variable aquatic processes such as diel metal cycling or episodic events is rarely feasible or cost-effective. Currently available automated samplers are a proven, widely used technology and typically collect up to 24 samples during a deployment. However, these automated samplers are not well suited for long-term sampling in remote areas or in freezing conditions. There is a critical need for low-cost, long-duration, high-frequency water sampling technology to improve our understanding of the geochemical response to temporally variable processes. This review article will examine recent developments in automated water sampler technology and utilize selected field data from acid mine drainage studies to illustrate the utility of high-frequency, long-duration water sampling.

  12. 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.

  13. Sampling design and procedures for fixed surface-water sites in the Georgia-Florida coastal plain study unit, 1993

    Science.gov (United States)

    Hatzell, H.H.; Oaksford, E.T.; Asbury, C.E.

    1995-01-01

    The implementation of design guidelines for the National Water-Quality Assessment (NAWQA) Program has resulted in the development of new sampling procedures and the modification of existing procedures commonly used in the Water Resources Division of the U.S. Geological Survey. The Georgia-Florida Coastal Plain (GAFL) study unit began the intensive data collection phase of the program in October 1992. This report documents the implementation of the NAWQA guidelines by describing the sampling design and procedures for collecting surface-water samples in the GAFL study unit in 1993. This documentation is provided for agencies that use water-quality data and for future study units that will be entering the intensive phase of data collection. The sampling design is intended to account for large- and small-scale spatial variations, and temporal variations in water quality for the study area. Nine fixed sites were selected in drainage basins of different sizes and different land-use characteristics located in different land-resource provinces. Each of the nine fixed sites was sampled regularly for a combination of six constituent groups composed of physical and chemical constituents: field measurements, major ions and metals, nutrients, organic carbon, pesticides, and suspended sediments. Some sites were also sampled during high-flow conditions and storm events. Discussion of the sampling procedure is divided into three phases: sample collection, sample splitting, and sample processing. A cone splitter was used to split water samples for the analysis of the sampling constituent groups except organic carbon from approximately nine liters of stream water collected at four fixed sites that were sampled intensively. An example of the sample splitting schemes designed to provide the sample volumes required for each sample constituent group is described in detail. Information about onsite sample processing has been organized into a flowchart that describes a pathway for each of

  14. Interstitial water studies on small core samples, Deep Sea Drilling Project, Leg 5

    Science.gov (United States)

    Manheim, F. T.; Chan, K.M.; Sayles, F.L.

    1970-01-01

    Leg 5 samples fall into two categories with respect to interstitial water composition: 1) rapidly deposited terrigenous or appreciably terrigenous deposits, such as in Hole 35 (western Escanaba trough, off Cape Mendocino, California); and, 2) slowly deposited pelagic clays and biogenic muds and oozes. Interstitial waters in the former show modest to slight variations in chloride and sodium, but drastic changes in non-conservative ions such as magnesium and sulfate. The pelagic deposits show only relatively minor changes in both conservative and non-conservative pore fluid constituents. As was pointed out in earlier Leg Reports, it is believed that much of the variation in chloride in pore fluids within individual holes is attributable to the manipulation of samples on board ship and in the laboratory. On the other hand, the scatter in sodium is due in part to analytical error (on the order of 2 to 3 per cent, in terms of a standard deviation), and it probably accounts for most of the discrepancies in total anion and cation balance. All constituents reported here, with the exception of bulk water content, were analyzed on water samples which were sealed in plastic tubes aboard ship and were subsequently opened and divided into weighed aliquots in the laboratory. Analytical methods follow the atomic absorption, wet chemical and emission spectrochemical techniques briefly summarized in previous reports, e.g. Manheim et al., 1969, and Chan and Manheim, 1970. The authors acknowledge assistance from W. Sunda, D. Kerr, C. Lawson and H. Richards, and thank D. Spencer, P. Brewer and E. Degens for allowing the use of equipment and laboratory facilities.

  15. Replica exchange with solute tempering: A method for sampling biological systems in explicit water

    Science.gov (United States)

    Liu, Pu; Kim, Byungchan; Friesner, Richard A.; Berne, B. J.

    2005-09-01

    An innovative replica exchange (parallel tempering) method called replica exchange with solute tempering (REST) for the efficient sampling of aqueous protein solutions is presented here. The method bypasses the poor scaling with system size of standard replica exchange and thus reduces the number of replicas (parallel processes) that must be used. This reduction is accomplished by deforming the Hamiltonian function for each replica in such a way that the acceptance probability for the exchange of replica configurations does not depend on the number of explicit water molecules in the system. For proof of concept, REST is compared with standard replica exchange for an alanine dipeptide molecule in water. The comparisons confirm that REST greatly reduces the number of CPUs required by regular replica exchange and increases the sampling efficiency. This method reduces the CPU time required for calculating thermodynamic averages and for the ab initio folding of proteins in explicit water. Author contributions: B.J.B. designed research; P.L. and B.K. performed research; P.L. and B.K. analyzed data; and P.L., B.K., R.A.F., and B.J.B. wrote the paper.Abbreviations: REST, replica exchange with solute tempering; REM, replica exchange method; MD, molecular dynamics.*P.L. and B.K. contributed equally to this work.

  16. Comparison of filters for concentrating microbial indicators and pathogens in lake-water samples

    Science.gov (United States)

    Francy, Donna S.; Stelzer, Erin A.; Brady, Amie M.G.; Huitger, Carrie; Bushon, Rebecca N.; Ip, Hon S.; Ware, Michael W.; Villegas, Eric N.; Gallardo, Vincent; Lindquist, H.D. Alan

    2013-01-01

    Bacterial indicators are used to indicate increased health risk from pathogens and to make beach closure and advisory decisions; however, beaches are seldom monitored for the pathogens themselves. Studies of sources and types of pathogens at beaches are needed to improve estimates of swimming-associated health risks. It would be advantageous and cost-effective, especially for studies conducted on a regional scale, to use a method that can simultaneously filter and concentrate all classes of pathogens from the large volumes of water needed to detect pathogens. In seven recovery experiments, stock cultures of viruses and protozoa were seeded into 10-liter lake water samples, and concentrations of naturally occurring bacterial indicators were used to determine recoveries. For the five filtration methods tested, the highest median recoveries were as follows: glass wool for adenovirus (4.7%); NanoCeram for enterovirus (14.5%) and MS2 coliphage (84%); continuous-flow centrifugation (CFC) plus Virocap (CFC+ViroCap) for Escherichia coli (68.3%) and Cryptosporidium (54%); automatic ultrafiltration (UF) for norovirus GII (2.4%); and dead-end UF for Enterococcus faecalis (80.5%), avian influenza virus (0.02%), and Giardia (57%). In evaluating filter performance in terms of both recovery and variability, the automatic UF resulted in the highest recovery while maintaining low variability for all nine microorganisms. The automatic UF was used to demonstrate that filtration can be scaled up to field deployment and the collection of 200-liter lake water samples.

  17. Extravascular lung water: its measurement by simultaneous pulmonary and aortic sampling and iterative convolution

    International Nuclear Information System (INIS)

    Giuntini, C.; Fazio, F.

    1975-01-01

    The inadequacy of the apparent distribution volume of THO during the first passage dilution curve (a) to account for the total lung water in in-vitro measurements in dogs and (b) to measure any increase in lung water, even in patients with obvious clinical pulmonary oedema, prompted the present investigation. Tritiated water, THO, as diffusible indicator, and human serum albumin labelled with 131 I, ALB, as intravascular tracer, are injected into the superior vena cava at the junction with the right atrium. In order to clear the aortic blood samples of recirculation, the recirculating tracers must be determined. This is accomplished by pulmonary artery sampling. Iterative convolution of the pulmonary artery dilution curves with suitable test functions eventually yields products of convolution that fit well the corresponding aortic dilution curves of THO and ALB. The test functions that yield the best fit are taken to represent the frequency functions of the transit time from pulmonary artery to aorta of THO and ALB, respectively. By applying the same procedure of iterative convolution to these frequency functions, we obtain the dilution curve of THO in the extravascular lung space. As a result of this analysis: (a) forward extrapolation is less subject to systematic errors such as overestimation of the mean transit time of ALB, i.e. of the tracer that recirculates more; and (b) the distribution volume of THO can be better defined since the dilution of THO in the extravascular lung space may be followed beyond the point of recirculation. The results indicate that both in normal subjects and in patients with left ventricular insufficiency the computed dilution curves of THO in the extravascular lung space have a long tail which is more pronounced in the patients. These findings suggest the existence in the lungs of extravascular water pools that are slowly exchanging with pulmonary water flow. This may depend both on inhomogeneities of perfusion, with lack of it at

  18. Study of lead pollution in air, soil and water samples of Quetta city

    International Nuclear Information System (INIS)

    Khan, M.; Khan, G.M.; Akbar, S.; Panezai, M.A.; Haq, Z.U.

    2011-01-01

    This study briefly presents the collected data of lead pollution in the environment of Quetta City in Balochistan, Pakistan. The samples were collected from different sites. The analysis of lead was carried out in underground water samples, the exhaust of different vehicles, roadside and sewage soils from selected points of Quetta City. The average discharge resulted in deposition by motorcycles (29.12 g/h), cars (44.47 g/h), wagons (176.54 g/h) and buses (141.52 g/h). The maximum deposition was 222.96 g/h from auto-rickshaws. The value for lead in smoke of different vehicles seems quite high when extrapolated to the large number of such vehicles for a longer time. The concentration of lead in roadside soil varied from 73.3 mg/kg (T and T closed colony) to 731.9 mg/kg (Sirki road bus-stop). The average content of lead in sewage soil of City Nala is 1250.6 mg/kg. The level of lead was more than WHO standards for such soils. The lead quantity in all 24 tube- well water samples, was slightly above the WHO standards (10 macro g/L).The results of this study were comparable to similar study in twin cities of Rawalpindi and islamabad. (author)

  19. Reverse flow injection spectrophotometric determination of thiram and nabam fungicides in natural water samples

    International Nuclear Information System (INIS)

    Asghar, M.; Yaqoob, M.; Nabi, A.

    2014-01-01

    A reverse flow injection (rFI) spectrophotometric method is reported for determination of thiram and nabam fungicides in natural water samples. The method is based on the reduction of iron(III) in the presence of thiram/nabam in acidic medium at 60 degree C and formation of iron(II)-ferricyanide complex was measured at 790 nm. The limits of detection (3s blank) were 0.01 and 0.05 micro g mL1 for thiram and nabam respectively with a sample throughput of 60 h1. Calibration graphs were linear over the range of 0.02 - 8.0 micro g mL1 (R2 = 0.9999, n = 8) and 0.1 - 30 micro g mL1 (R2 = 0.9982, n = 10) for thiram and nabam with relative standard deviations (RSDs; n = 3) in the range of 0.8 - 1.6% respectively. Experimental parameters and potential interferences were examined. Thiram and nabam were determined in natural water samples using solid-phase extraction (SPE) procedure and recoveries were in the range of 93+-3 - 105+-2% and 87+-4 - 102+-3% respectively. The results obtained were not significantly different compared with a HPLC method. (author)

  20. Microporous Carbon Spheres Solid Phase Membrane Tip Extraction for the Analysis of Nitrosamines in Water Samples

    International Nuclear Information System (INIS)

    Mohammed Salisu Musa; Wan Aini Wan Ibrahim

    2015-01-01

    A simple solid phase membrane tip extraction (SPMTE) utilizing microporous carbon spheres (MCS) was developed for the analysis of nitrosamines in aqueous samples. The method termed MCS-SPMTE was optimized for various important extraction parameters namely conditioning organic solvent, extraction time, effects of salt addition and pH change, desorption time, desorption solvent and sample volume. Under the optimized conditions, the method indicated good linearity in the range of 10-100 μg/ L with coefficients of determination, r 2 ≥0.9984. The method also demonstrated good reproducibility with % RSDs values ranging from 2.2 - 8.9 (n = 3). Limit of detection (LOD) and limit of quantification (LOQ) for the method ranged from 3.2 - 4.8 μg/ L and 10.9 - 15.9 μg/L respectively. Recoveries for both tap-water and lake water samples spiked at 10 μg/L were in the range of 83.2 - 107.5 %. (author)

  1. HPLC determination of chlorine in air and water samples following precolumn derivatization to 4-bromoacetanilide

    Energy Technology Data Exchange (ETDEWEB)

    Jain, A. (Rani Durgavati Univ., Jabalpur (India). Dept. of Chemistry); Verma, K.K. (Rani Durgavati Univ., Jabalpur (India). Dept. of Chemistry)

    1993-11-01

    Chlorine has been determined in air and water samples by a rapid and sensitive method entailing precolumn derivatization to 4-bromoacetanilide. A mixed potassium bromide - acetanilide reagent was used as a trapping agent for chlorine in air, and for its derivatization. The 4-bromoacetanilide formed was determined by reversed-phase HPLC on an ODS column, using methanol-water, 65:35 (v/v) as mobile phase; detection was at 240 nm. A rectilinear calibration graph was obtained for the range 0.1-30 [mu]g mL[sup -1] chlorine; the limit of detection found to be 0.01 [mu]g mL[sup -1]. The precolumn derivative has been found to have a shelf-life of at least 21 days; this enables the use of the method for samples transported from the field to the analytical laboratory, or the testing of a variety of conditions for chlorine scrubbing studies without the need for immediate analysis of samples. Humic substances do not cause any interference with the proposed method and the presence of nitrite does not lead to artificially high results and consequent misleading conclusions of the presence of high levels of chlorine. (orig.)

  2. HPLC determination of chlorine in air and water samples following precolumn derivatization to 4-bromoacetanilide

    International Nuclear Information System (INIS)

    Jain, A.; Verma, K.K.

    1993-01-01

    Chlorine has been determined in air and water samples by a rapid and sensitive method entailing precolumn derivatization to 4-bromoacetanilide. A mixed potassium bromide - acetanilide reagent was used as a trapping agent for chlorine in air, and for its derivatization. The 4-bromoacetanilide formed was determined by reversed-phase HPLC on an ODS column, using methanol-water, 65:35 (v/v) as mobile phase; detection was at 240 nm. A rectilinear calibration graph was obtained for the range 0.1-30 μg mL -1 chlorine; the limit of detection found to be 0.01 μg mL -1 . The precolumn derivative has been found to have a shelf-life of at least 21 days; this enables the use of the method for samples transported from the field to the analytical laboratory, or the testing of a variety of conditions for chlorine scrubbing studies without the need for immediate analysis of samples. Humic substances do not cause any interference with the proposed method and the presence of nitrite does not lead to artificially high results and consequent misleading conclusions of the presence of high levels of chlorine. (orig.)

  3. Magnetic hydrophilic-lipophilic balance sorbent for efficient extraction of chemical warfare agents from water samples.

    Science.gov (United States)

    Singh, Varoon; Purohit, Ajay Kumar; Chinthakindi, Sridhar; Goud D, Raghavender; Tak, Vijay; Pardasani, Deepak; Shrivastava, Anchal Roy; Dubey, Devendra Kumar

    2016-02-19

    Magnetic hydrophilic-lipophilic balance (MHLB) hybrid resin was prepared by precipitation polymerization using N-vinylpyrrolidone (PVP) and divinylbenzene (DVB) as monomers and Fe2O3 nanoparticles as magnetic material. These resins were successfully applied for the extraction of chemical warfare agents (CWAs) and their markers from water samples through magnetic dispersive solid-phase extraction (MDSPE). By varying the ratios of monomers, resin with desired hydrophilic-lipophilic balance was prepared for the extraction of CWAs and related esters of varying polarities. Amongst different composites Fe2O3 nanoparticles coated with 10% PVP+90% DVB exhibited the best recoveries varying between 70.32 and 97.67%. Parameters affecting the extraction efficiencies, such as extraction time, desorption time, nature and volume of desorption solvent, amount of extraction sorbent and the effect of salts on extraction were investigated. Under the optimized conditions, linearity was obtained in the range of 0.5-500 ng mL(-1) with correlation ranging from 0.9911-0.9980. Limits of detection and limits of quantification were 0.5-1.0 and 3.0-5.0 ng mL(-1) respectively with RSDs varying from 4.88-11.32% for markers of CWAs. Finally, the developed MDSPE method was employed for extraction of analytes from water samples of various sources and the OPCW proficiency test samples. Copyright © 2016 Elsevier B.V. All rights reserved.

  4. Molecular characterization of viable Legionella spp. in cooling tower water samples by combined use of ethidium monoazide and PCR.

    Science.gov (United States)

    Inoue, Hiroaki; Fujimura, Reiko; Agata, Kunio; Ohta, Hiroyuki

    2015-01-01

    Viable Legionella spp. in environmental water samples were characterized phylogenetically by a clone library analysis combining the use of ethidium monoazide and quantitative PCR. To examine the diversity of Legionella spp., six cooling tower water samples and three bath water samples were collected and analyzed. A total of 617 clones were analyzed for their 16S rRNA gene sequences and classified into 99 operational taxonomic units (OTUs). The majority of OTUs were not clustered with currently described Legionella spp., suggesting the wide diversity of not-yet-cultured Legionella groups harbored in cooling tower water environments.

  5. Ten years of radiometric monitoring in water samples in Uruguay potables plants

    International Nuclear Information System (INIS)

    Perruni, P.

    2000-01-01

    The work exposes the summary of having been radiometrics obtained during the last 10 years in several water treatment plants of the national territory, with the purpose of determining if in the total dose to the one that this exposed one naturally the population of the country, is important the contribution of polluting radioactives in the drinkable water, in function of the geographical area and the time of the year. The investigation is framed inside the Program of Control Radiometrics of Products of Fission in waters, floors, foods and aerosols of the Uruguay developed by the Radiochemistry Department, of the Nuclear Research Center, Montevideo (UY) The samples of water filter, they process and they analyze according to laboratory protocols, had duplicated by each plant, parallel with radio-active, white bottom measures and standards. The results net average obtained for each factory, gave below the one it limits of detection: 2 BQ/Kg for geometry Marinelli and 0.02 BQ/g for plane geometry, with 99,3% of dependability (standard 3 deviations), very below the maximum values admitted by International Organisms (WHO, FAO, ICRP) [es

  6. Solid phase extraction for the speciation and preconcentration of inorganic selenium in water samples: a review.

    Science.gov (United States)

    Herrero Latorre, C; Barciela García, J; García Martín, S; Peña Crecente, R M

    2013-12-04

    Selenium is an essential element for the normal cellular function of living organisms. However, selenium is toxic at concentrations of only three to five times higher than the essential concentration. The inorganic forms (mainly selenite and selenate) present in environmental water generally exhibit higher toxicity (up to 40 times) than organic forms. Therefore, the determination of low levels of different inorganic selenium species in water is an analytical challenge. Solid-phase extraction has been used as a separation and/or preconcentration technique prior to the determination of selenium species due to the need for accurate measurements for Se species in water at extremely low levels. The present paper provides a critical review of the published methods for inorganic selenium speciation in water samples using solid phase extraction as a preconcentration procedure. On the basis of more than 75 references, the different speciation strategies used for this task have been highlighted and classified. The solid-phase extraction sorbents and the performance and analytical characteristics of the developed methods for Se speciation are also discussed. Copyright © 2013 Elsevier B.V. All rights reserved.

  7. Alkaline Peptone Water-Based Enrichment Method for mcr-3 From Acute Diarrheic Outpatient Gut Samples

    Directory of Open Access Journals (Sweden)

    Qiaoling Sun

    2018-05-01

    Full Text Available A third plasmid-mediated colistin resistance gene, mcr-3, is increasingly being reported in Enterobacteriaceae and Aeromonas spp. from animals and humans. To investigate the molecular epidemiology of mcr in the gut flora of Chinese outpatients, 152 stool specimens were randomly collected from outpatients in our hospital from May to June, 2017. Stool specimens enriched in alkaline peptone water or Luria-Bertani (LB broth were screened for mcr-1, mcr-2, and mcr-3 using polymerase chain reaction (PCR-based assays. Overall, 19.1% (29/152 and 5.3% (8/152 of the stool samples enriched in alkaline peptone water were PCR-positive for mcr-1 and mcr-3, respectively, while 2.7% (4/152 of samples were positive for both mcr-1 and mcr-3. Strains isolated from the samples that were both mcr-1- and mcr-3-positive were subjected to antimicrobial susceptibility testing by broth microdilution. They were also screened for the presence of other resistance genes by PCR, while multilocus sequence typing and whole-genome sequencing were used to investigate the molecular epidemiology and genetic environment, respectively, of the resistance genes. mcr-3-positive Aeromonas veronii strain 126-14, containing a mcr-3.8-mcr-3-like2 segment, and mcr-1-positive Escherichia coli strain 126-1, belonging to sequence type 1485, were isolated from the sample from a diarrheic butcher with no history of colistin treatment. A. veronii 126-14 had a colistin minimum inhibitory concentration (MIC of 2 µg/mL and was susceptible to antibiotics in common use, while E. coli 126-1 produced TEM-1, CTX-M-55, and CTX-M-14 β-lactamases and was resistant to colistin, ceftazidime, and cefotaxime. Overall, there was a higher detection rate of mcr-3-carrying strains with low colistin MICs from the samples enriched in alkaline peptone water than from samples grown in LB broth.

  8. Correlation of lithium levels between drinking water obtained from different sources and scalp hair samples of adult male subjects.

    Science.gov (United States)

    Baloch, Shahnawaz; Kazi, Tasneem Gul; Afridi, Hassan Imran; Baig, Jameel Ahmed; Talpur, Farah Naz; Arain, Muhammad Balal

    2017-10-01

    There is some evidence that natural levels of lithium (Li) in drinking water may have a protective effect on neurological health. In present study, we evaluate the Li levels in drinking water of different origin and bottled mineral water. To evaluate the association between lithium levels in drinking water with human health, the scalp hair samples of male subjects (25-45 years) consumed drinking water obtained from ground water (GW), municipal treated water (MTW) and bottled mineral water (BMW) from rural and urban areas of Sindh, Pakistan were selected. The water samples were pre-concentrated five to tenfold at 60 °C using temperature-controlled electric hot plate. While scalp hair samples were oxidized by acid in a microwave oven, prior to determined by flame atomic absorption spectrometry. The Li content in different types of drinking water, GW, MTW and BMW was found in the range of 5.12-22.6, 4.2-16.7 and 0.0-16.3 µg/L, respectively. It was observed that Li concentration in the scalp hair samples of adult males consuming ground water was found to be higher, ranged as 292-393 μg/kg, than those who are drinking municipal treated and bottle mineral water (212-268 and 145-208 μg/kg), respectively.

  9. Heavy Metals in Salt and Water Samples from Maharloo Lake and their Comparison with Metal Concentrations in Samples from Sirjan, Lar, and Firoozabad Salt Mines

    Directory of Open Access Journals (Sweden)

    Farahnaz Sabet

    2015-03-01

    Full Text Available Maharloo Lake is one of the most important water ecosystems in Iran, which is nowadays exposed to multiple risks and threats due to poor water management, salt extraction, and heavy metal pollution. In this study, the concentrations of such heavy metals as chromium, copper, zinc, arsenic, cadmium, and lead in both water and salt samples collected from areas in the north and south of the lake were determined by atomic absorption (AA-670G after the samples had been digested. Results showed that metal concentrations in the salt samples taken from both the northern and southern areas had identical mean values in the order of Cr> Cu> As> Cd> Pb. An almost similar pattern was detected in metal concentrations in water samples taken from the same areas but with a slight difference in the way they were ordered (Cr> Cu> As> Pb> Cd. It was found that both water and salt samples collected from the northern areas had higher metal concentrations, except for that of Pb which was slightly lower. Comparison of the mean values of metal concentrations in the Salt Lake and those of Sirjan, Lar, and Firoozabad salt mines revealed that copper, cadmium, and lead had their highest concentrations in the Salt Lake while arsenic and chromium recorded their highest values in samples taken from Lar and Firoozabad salt mines, respectively. Based on these findings, it may be concluded that the increased metal concentrations observed in samples from both northern and southern areas of the lake are due to the sewage and effluents from urban, industrial, and hospital sources in Shiraz disposed into the lake as well as such other human activities as farming in the areas around the lake, especially in the northern stretches. These observations call for preventive measures to avoid further water quality degradation in the area.

  10. Trace analysis of iron in environmental water and snow samples from Poland

    International Nuclear Information System (INIS)

    Golimowski, J.

    1989-01-01

    A voltammetric method for the determination of iron at detection limit of 4 μg/l is described, using the catalytic current of the reduction of the Fe(III)-triethanolamine (TEA) complex in the presence of bromate ions. The determination was performed at a mercury hanging drop electrode without preconcentration, using the TEA alkaline solution as a supporting electrolyte and the differential pulse technique. A peak current for the Fe-(III)-TEA catalytic reduction was observed at a potential of -1.0 V (Ag/AgCl saturated electrode). The influence of TEA, BrO 3 and NaOH concentrations on the peak height was studied. It was found that a 100-fold excess of Mn, a 50-fold excess of Cr(VI) and Zn did not interfere in the determination. This method was applied to the determination of iron in water, snow and waste water samples

  11. Evaluation of lyophilization for the preconcentration of natural water samples prior to neutron activation analysis

    International Nuclear Information System (INIS)

    Harrison, S.H.; LaFleur, P.D.; Zoller, W.H.

    1975-01-01

    Water is preconcentrated by freeze drying using a method which virtually eliminates sample contamination and trace element losses. To test the possibility of losses of volatile elements during the drying process, known quantities of radioactive tracers for 21 elements were added to water, the solutions freeze dried, and the tracer residues counted. The results confirm that at least 95 percent of all but the most volatile elements studied (Hg and I) were retained in the residue. The problem of transferring quantitatively the dry residue from the freeze drying container to an irradiation container was eliminated by designing a freeze drying container that would also serve as an irradiation and counting container. (U.S.)

  12. Data Validation Package - April and July 2015 Groundwater and Surface Water Sampling at the Gunnison, Colorado, Processing Site

    Energy Technology Data Exchange (ETDEWEB)

    Linard, Joshua [Dept. of Energy (DOE), Washington, DC (United States). Office of Legacy Management; Campbell, Sam [Navarro Research and Engineering, Inc., Oak Ridge, TN (United States)

    2016-02-01

    This event included annual sampling of groundwater and surface water locations at the Gunnison, Colorado, Processing Site. Sampling and analyses were conducted as specified in Sampling and Analysis Plan for U.S. Department of Energy Office of Legacy Management Sites. Samples were collected from 28 monitoring wells, three domestic wells, and six surface locations in April at the processing site as specified in the 2010 Ground Water Compliance Action Plan for the Gunnison, Colorado, Processing Site. Domestic wells 0476 and 0477 were sampled in July because the homes were unoccupied in April, and the wells were not in use. Duplicate samples were collected from locations 0113, 0248, and 0477. One equipment blank was collected during this sampling event. Water levels were measured at all monitoring wells that were sampled. No issues were identified during the data validation process that requires additional action or follow-up.

  13. Analytical results for 544 water samples collected in the Attean Quartz Monzonite in the vicinity of Jackman, Maine

    Science.gov (United States)

    Ficklin, W.H.; Nowlan, G.A.; Preston, D.J.

    1983-01-01

    Water samples were collected in the vicinity of Jackman, Maine as a part of the study of the relationship of dissolved constituents in water to the sediments subjacent to the water. Each sample was analyzed for specific conductance, alkalinity, acidity, pH, fluoride, chloride, sulfate, phosphate, nitrate, sodium, potassium, calcium, magnesium, and silica. Trace elements determined were copper, zinc, molybdenum, lead, iron, manganese, arsenic, cobalt, nickel, and strontium. The longitude and latitude of each sample location and a sample site map are included in the report as well as a table of the analytical results.

  14. An easy method for the determination of Ra isotopes and actinide alpha emitters from the same water sample

    International Nuclear Information System (INIS)

    Moron, M.C.; Garcia-Tenorio, R.; Garcia-Montano, E.; Garcia-Leon, M.; Madurga, G.

    1986-01-01

    Radium isotopes and actinide α emitters are easily determined from the same water sample. The Ra fraction is obtained by coprecipitation with Ba, while a Fe coprecipitation is used for the actinides. Both fractions are measured with a gas-flow proportional counter. Additionally the isotopic Ra composition is obtained by measuring at two or three different times the α activity from the Ra-fraction. The method is applied to rain water and drinking water samples. (author)

  15. Analysis of {sup 210}Pb in water samples with plastic scintillation resins

    Energy Technology Data Exchange (ETDEWEB)

    Lluch, E.; Barrera, J. [Department of Analytical Chemistry, University of Barcelona, Martí i Franqués, 1-11, E-08028, Barcelona (Spain); Tarancón, A., E-mail: alex.tarancon@ub.edu [Department of Analytical Chemistry, University of Barcelona, Martí i Franqués, 1-11, E-08028, Barcelona (Spain); Bagán, H. [Department of Pure and Applied Biochemistry, Lund University, Getingevägen 60, Hus II, 22100 SE, Lund (Sweden); García, J.F. [Department of Analytical Chemistry, University of Barcelona, Martí i Franqués, 1-11, E-08028, Barcelona (Spain)

    2016-10-12

    {sup 210}Pb is a radioactive lead isotope present in the environment as member of the {sup 238}U decay chain. Since it is a relatively long-lived radionuclide (T{sub 1/2} = 22.2 years), its analysis is of interest in radiation protection and the geochronology of sediments and artwork. Here, we present a method for analysing {sup 210}Pb using plastic scintillation resins (PSresins) packaged in solid-phase extraction columns (SPE cartridge). The advantages of this method are its selectivity, the low limit of detection, as well as reductions in the amount of time and reagents required for analysis and the quantity of waste generated. The PSresins used in this study were composed of a selective extractant (4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6 in 1-octanol) covering the surface of plastic scintillation microspheres. Once the amount of extractant (1:1/4) and medium of separation (2 M HNO{sub 3}) were optimised, PSresins in SPE cartridges were calibrated with a standard solution of {sup 210}Pb. {sup 210}Pb could be fully separated from its daughters, {sup 210}Bi and {sup 210}Po, with a recovery value of 91(3)% and detection efficiency of 44(3)%. Three spiked water samples (one underground and two river water samples) were analysed in triplicates with deviations lower than 10%, demonstrating the validity of the PS resin method for {sup 210}Pb analysis. - Highlights: • A plastic scintillation resin for selective analysis of {sup 210}Pb has been developed. • A commercial SPE cartridge has been use for separation and scintillation counting. • {sup 210}Pb separation from {sup 210}Bi and {sup 210}Po is achieved with a 91(3)% of recovery. • The method is valid for analysis of {sup 210}Pb in river water samples.

  16. A comparison of surface water natural organic matter in raw filtered water samples, XAD, and reverse osmosis isolates

    Science.gov (United States)

    Maurice, P.A.; Pullin, M.J.; Cabaniss, S.E.; Zhou, Q.; Namjesnik-Dejanovic, K.; Aiken, G.R.

    2002-01-01

    This research compared raw filtered waters (RFWs), XAD resin isolates (XAD-8 and XAD-4), and reverse osmosis (RO) isolates of several surface water samples from McDonalds Branch, a small freshwater fen in the New Jersey Pine Barrens (USA). RO and XAD-8 are two of the most common techniques used to isolate natural organic matter (NOM) for studies of composition and reactivity; therefore, it is important to understand how the isolates differ from bulk (unisolated) samples and from one another. Although, any comparison between the isolation methods needs to consider that XAD-8 is specifically designed to isolate the humic fraction, whereas RO concentrates a broad range of organic matter and is not specific to humics. The comparison included for all samples: weight average molecular weight (Mw), number average molecular weight (Mn), polydispersity (??), absorbance at 280nm normalized to moles C (??280) (RFW and isolates); and for isolates only: elemental analysis, % carbon distribution by 13C NMR, and aqueous FTIR spectra. As expected, RO isolation gave higher yield of NOM than XAD-8, but also higher ash content, especially Si and S. Mw decreased in the order: RO>XAD-8>RFW>XAD-4. The Mw differences of isolates compared with RFW may be due to selective isolation (fractionation), or possibly in the case of RO to condensation or coagulation during isolation. 13C NMR results were roughly similar for the two methods, but the XAD-8 isolate was slightly higher in 'aromatic' C and the RO isolate was slightly higher in heteroaliphatic and carbonyl C. Infrared spectra indicated a higher carboxyl content for the XAD-8 isolates and a higher ester:carboxyl ratio for the RO isolates. The spectroscopic data thus are consistent with selective isolation of more hydrophobic compounds by XAD-8, and also with potential ester hydrolysis during that process, although further study is needed to determine whether ester hydrolysis does indeed occur. Researchers choosing between XAD and RO

  17. Evaluation of methods to sample fecal indicator bacteria in foreshore sand and pore water at freshwater beaches.

    Science.gov (United States)

    Vogel, Laura J; Edge, Thomas A; O'Carroll, Denis M; Solo-Gabriele, Helena M; Kushnir, Caitlin S E; Robinson, Clare E

    2017-09-15

    Fecal indicator bacteria (FIB) are known to accumulate in foreshore beach sand and pore water (referred to as foreshore reservoir) where they act as a non-point source for contaminating adjacent surface waters. While guidelines exist for sampling surface waters at recreational beaches, there is no widely-accepted method to collect sand/sediment or pore water samples for FIB enumeration. The effect of different sampling strategies in quantifying the abundance of FIB in the foreshore reservoir is unclear. Sampling was conducted at six freshwater beaches with different sand types to evaluate sampling methods for characterizing the abundance of E. coli in the foreshore reservoir as well as the partitioning of E. coli between different components in the foreshore reservoir (pore water, saturated sand, unsaturated sand). Methods were evaluated for collection of pore water (drive point, shovel, and careful excavation), unsaturated sand (top 1 cm, top 5 cm), and saturated sand (sediment core, shovel, and careful excavation). Ankle-depth surface water samples were also collected for comparison. Pore water sampled with a shovel resulted in the highest observed E. coli concentrations (only statistically significant at fine sand beaches) and lowest variability compared to other sampling methods. Collection of the top 1 cm of unsaturated sand resulted in higher and more variable concentrations than the top 5 cm of sand. There were no statistical differences in E. coli concentrations when using different methods to sample the saturated sand. Overall, the unsaturated sand had the highest amount of E. coli when compared to saturated sand and pore water (considered on a bulk volumetric basis). The findings presented will help determine the appropriate sampling strategy for characterizing FIB abundance in the foreshore reservoir as a means of predicting its potential impact on nearshore surface water quality and public health risk. Copyright © 2017 Elsevier Ltd. All rights

  18. Determination of 222Rn in water samples from wells and springs in Tokyo by a modified integral counting method

    International Nuclear Information System (INIS)

    Homma, Y.; Murase, Y.; Handa, K.; Murakami, I.

    1997-01-01

    222 Rn in 2L-water samples was extracted with 30 mL toluene, and 21 mL of the toluene solution was transferred into a liquid scintillation vial, in which PPO - 2,5-diphenyloxazole was placed in advance. The total activity of 222 Rn in the water sample was calculated based on the Ostwald's coefficient of solubilities of 222 Rn in toluene and water at the temperature of the sample water and the volume of water and toluene. About 40% of 222 Rn dissolved in 2L-water sample can be collected. After allowing to stand for 3.5 h, the equilibrium mixture of 222 Rn and its daughters was measured with an Aloka liquid scintillation spectrometer using a modified integral counting method which extrapolates the integral counting curve not to the zero pulse-height, but to the zero detection threshold, an average energy required to produce a measurable pulse, of the liquid scintillation spectrometer. The general method which agitates water sample (usually about 10 mL) with a liquid scintillation cocktail is practical when the activity of 222 Rn is high. By adding 10 mL of water sample, however, it is possible also to add variable amounts of quencher. In some cases water sample is preserved with nitric acid. The slope of the integral counting rate curve increases as quench level of the sample increases. Therefore, it is clear that the modified integral counting method gives more accurate 222 Rn concentrations for water samples of strong quench than the conventional integral counting method. 222 Rn sample of 0.2 Bq/L can be determined within an overall uncertainty of 3.1%

  19. 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

  20. A rapid method of radium-226 analysis in water samples using an alpha spectroscopic technique

    International Nuclear Information System (INIS)

    Lim, T.P.

    1981-01-01

    A fast, reliable and accurate method for radium-226 determination in environmental water samples has been devised, using an alpha spectroscopic technique. The correlation between barium-133 and radium-226 in the barium-radium sulphate precipitation mechanism was studied and in the limited experimental recovery range, the coefficient of correlation was r = 0.986. A self-absorption study for various barium carrier concentrations was also undertaken to obtain the least broadening of alpha energy line widths. An optimum value of 0.3 mg barium carrier was obtained for chemical recovery in the range of 85 percent. (auth)

  1. Measurement of tissue free water tritium in biological samples by liquid scintillation counter

    International Nuclear Information System (INIS)

    Wu Zongmei; Zheng Xiaomin

    1993-01-01

    The authors introduced a method of extracting tissue free water tritium (TFWT) by the azeotropic distribution with toluene and of measuring the activity of the TFWT in biological samples by liquid scintillation counter. The TFWT recovery ratio of pine needles (fresh), green vegetables, radish, rice, pork (muscle) and milk is 0.90, 0.95, 0.96, 0.90, 0.52 and 0.85, and TFWT activity is 1.8, 3.2, 1.8, 2.7, 3.3 and 4.0 Bq/L-H 2 O, respectively

  2. Investigation of the effects of various water mediums on desulfurization and deashing of a coal sample by flotation

    Energy Technology Data Exchange (ETDEWEB)

    Ayhan, F.D. [Dicle University, Diyarbakir (Turkey)

    2009-08-15

    The aim of this study was to investigate the effects of various water mediums on desulfurization and deashing of a coal sample using flotation. For this purpose, experimental studies were conducted on a coal sample containing high ash and sulfur contents. The effects of pH, solid concentration, collector amount and frother amount on the flotation were investigated separately in Mediterranean Sea water, Cermik thermal spring water, snow water and tap water. Flotation, results indicated that, when comparing the various water mediums, the following order for the ash content was obtained: snow water < Cermik thermal spring water < tap water < the Mediterranean Sea water. For the reduction of total sulfur, the following order was obtained: snow water > Cermik thermal spring water > Mediterranean Sea water > tap water. When snow water was used as a flotation medium, it was found that a concentrate containing 3.01% total sulfur and 27.64% ash with a total sulfur reduction of 57.06% was obtained from a feed containing 7.01% total sulfur and 4.1.17% ash.

  3. Spatial statistics of hydrography and water chemistry in a eutrophic boreal lake based on sounding and water samples.

    Science.gov (United States)

    Leppäranta, Matti; Lewis, John E; Heini, Anniina; Arvola, Lauri

    2018-06-04

    Spatial variability, an essential characteristic of lake ecosystems, has often been neglected in field research and monitoring. In this study, we apply spatial statistical methods for the key physics and chemistry variables and chlorophyll a over eight sampling dates in two consecutive years in a large (area 103 km 2 ) eutrophic boreal lake in southern Finland. In the four summer sampling dates, the water body was vertically and horizontally heterogenic except with color and DOC, in the two winter ice-covered dates DO was vertically stratified, while in the two autumn dates, no significant spatial differences in any of the measured variables were found. Chlorophyll a concentration was one order of magnitude lower under the ice cover than in open water. The Moran statistic for spatial correlation was significant for chlorophyll a and NO 2 +NO 3 -N in all summer situations and for dissolved oxygen and pH in three cases. In summer, the mass centers of the chemicals were within 1.5 km from the geometric center of the lake, and the 2nd moment radius ranged in 3.7-4.1 km respective to 3.9 km for the homogeneous situation. The lateral length scales of the studied variables were 1.5-2.5 km, about 1 km longer in the surface layer. The detected spatial "noise" strongly suggests that besides vertical variation also the horizontal variation in eutrophic lakes, in particular, should be considered when the ecosystems are monitored.

  4. Uranium and coexisting element behaviour in surface waters and associated sediments with varied sampling techniques used for uranium exploration

    International Nuclear Information System (INIS)

    Wenrich-Verbeek, K.J.

    1977-01-01

    Optimum sampling methods in surface water and associated sediments for use in uranium exploration are being studied at thirty sites in Colorado, New Mexico, Arizona and Utah. For water samples, filtering is recommended to increase sample homogeneity and reproducibility because for most elements studied water samples which were allowed to remain unfiltered until time of analysis contained higher concentrations than field-filtered samples of the same waters. Acidification of unfiltered samples resulted in still higher concentrations. This is predominantly because of leaching of the elements from the suspended fraction. U in water correslates directly with Ca, Mg, Na, K, Ba, B, Li and As. In stream sediments, U and other trace elements are concentrated in the finer size fractions. Accordingly, in prospecting, grain size fractions less than 90 μm (170 mesh) should be analyzed for U. A greater number of elements (21) show a significant positive correlation with U in stream sediments than in water. Results have revealed that anomalous concentrations of U found in water may not be detected in associated sediments and vice versa. Hence, sampling of both surface water and coexisting sediment is strongly recommended

  5. Measurement of the wetting profile in concrete samples with vertical water by gamma radiation transmission method

    International Nuclear Information System (INIS)

    Silva, L.M. da; Rocha, M.C. da; Appoloni, C.R.; Portezan Filho, O.; Lopes, F.; Melquiades, F.L.; Santos, E.A. dos; Santos, A.O. dos; Moreira, A.C.; Poetker, W.E.; Almeida, E. de; Tannous, C.Q.; Kuramoto, R.; Cavalcante, F.H. de M.; Barbieri, P.F.

    2000-01-01

    Samples of concrete for popular habitation (0,1x0,03x0,1 m) and cellular concrete (0,1x0,05x0,1 m) were submitted to water vertical ascending infiltration. The moisture content spatial and temporal evolution of each sample it was monitored in three halfway positions in a same horizontal line, applying the gamma rays transmission method. The data were taken with a 137 Cs (3,7x10 10 Bq, 0662 MeV) source, NaI (Tl) of 2x2' detector coupled to between wetting profiles and concrete strength. The cellular concrete showed a wetting profile compatible to its greater porosity. (author)

  6. Simple Modification of Karl-Fischer Titration Method for Determination of Water Content in Colored Samples

    Science.gov (United States)

    Tavčar, Eva; Turk, Erika; Kreft, Samo

    2012-01-01

    The most commonly used technique for water content determination is Karl-Fischer titration with electrometric detection, requiring specialized equipment. When appropriate equipment is not available, the method can be performed through visual detection of a titration endpoint, which does not enable an analysis of colored samples. Here, we developed a method with spectrophotometric detection of a titration endpoint, appropriate for moisture determination of colored samples. The reaction takes place in a sealed 4 ml cuvette. Detection is performed at 520 nm. Titration endpoint is determined from the graph of absorbance plotted against titration volume. The method has appropriate reproducibility (RSD = 4.3%), accuracy, and linearity (R 2 = 0.997). PMID:22567558

  7. Simple Modification of Karl-Fischer Titration Method for Determination of Water Content in Colored Samples

    Directory of Open Access Journals (Sweden)

    Eva Tavčar

    2012-01-01

    Full Text Available The most commonly used technique for water content determination is Karl-Fischer titration with electrometric detection, requiring specialized equipment. When appropriate equipment is not available, the method can be performed through visual detection of a titration endpoint, which does not enable an analysis of colored samples. Here, we developed a method with spectrophotometric detection of a titration endpoint, appropriate for moisture determination of colored samples. The reaction takes place in a sealed 4 ml cuvette. Detection is performed at 520 nm. Titration endpoint is determined from the graph of absorbance plotted against titration volume. The method has appropriate reproducibility (RSD=4.3%, accuracy, and linearity (2=0.997.

  8. Simple modification of karl-Fischer titration method for determination of water content in colored samples.

    Science.gov (United States)

    Tavčar, Eva; Turk, Erika; Kreft, Samo

    2012-01-01

    The most commonly used technique for water content determination is Karl-Fischer titration with electrometric detection, requiring specialized equipment. When appropriate equipment is not available, the method can be performed through visual detection of a titration endpoint, which does not enable an analysis of colored samples. Here, we developed a method with spectrophotometric detection of a titration endpoint, appropriate for moisture determination of colored samples. The reaction takes place in a sealed 4 ml cuvette. Detection is performed at 520 nm. Titration endpoint is determined from the graph of absorbance plotted against titration volume. The method has appropriate reproducibility (RSD = 4.3%), accuracy, and linearity (R(2) = 0.997).

  9. SPR based immunosensor for detection of Legionella pneumophila in water samples

    Science.gov (United States)

    Enrico, De Lorenzis; Manera, Maria G.; Montagna, Giovanni; Cimaglia, Fabio; Chiesa, Maurizio; Poltronieri, Palmiro; Santino, Angelo; Rella, Roberto

    2013-05-01

    Detection of legionellae by water sampling is an important factor in epidemiological investigations of Legionnaires' disease and its prevention. To avoid labor-intensive problems with conventional methods, an alternative, highly sensitive and simple method is proposed for detecting L. pneumophila in aqueous samples. A compact Surface Plasmon Resonance (SPR) instrumentation prototype, provided with proper microfluidics tools, is built. The developed immunosensor is capable of dynamically following the binding between antigens and the corresponding antibody molecules immobilized on the SPR sensor surface. A proper immobilization strategy is used in this work that makes use of an important efficient step aimed at the orientation of antibodies onto the sensor surface. The feasibility of the integration of SPR-based biosensing setups with microfluidic technologies, resulting in a low-cost and portable biosensor is demonstrated.

  10. A multicenter study of viable PCR using propidium monoazide to detect Legionella in water samples.

    Science.gov (United States)

    Scaturro, Maria; Fontana, Stefano; Dell'eva, Italo; Helfer, Fabrizia; Marchio, Michele; Stefanetti, Maria Vittoria; Cavallaro, Mario; Miglietta, Marilena; Montagna, Maria Teresa; De Giglio, Osvalda; Cuna, Teresa; Chetti, Leonarda; Sabattini, Maria Antonietta Bucci; Carlotti, Michela; Viggiani, Mariagabriella; Stenico, Alberta; Romanin, Elisa; Bonanni, Emma; Ottaviano, Claudio; Franzin, Laura; Avanzini, Claudio; Demarie, Valerio; Corbella, Marta; Cambieri, Patrizia; Marone, Piero; Rota, Maria Cristina; Bella, Antonino; Ricci, Maria Luisa

    2016-07-01

    Legionella quantification in environmental samples is overestimated by qPCR. Combination with a viable dye, such as Propidium monoazide (PMA), could make qPCR (named then vPCR) very reliable. In this multicentre study 717 artificial water samples, spiked with fixed concentrations of Legionella and interfering bacterial flora, were analysed by qPCR, vPCR and culture and data were compared by statistical analysis. A heat-treatment at 55 °C for 10 minutes was also performed to obtain viable and not-viable bacteria. When data of vPCR were compared with those of culture and qPCR, statistical analysis showed significant differences (P 0.05). Overall this study provided a good experimental reproducibility of vPCR but also highlighted limits of PMA in the discriminating capability of dead and live bacteria, making vPCR not completely reliable. Copyright © 2016 Elsevier Inc. All rights reserved.

  11. Preliminary evaluation of new polymer matrix for solid-phase extraction of nonylphenol from water samples.

    Science.gov (United States)

    Guerreiro, António; Soares, Ana; Piletska, Elena; Mattiasson, Bo; Piletsky, Sergey

    2008-03-31

    Molecularly imprinted (MIP) and blank polymers with affinity for nonylphenol were designed using computational modelling. Chromatographic tests demonstrated higher affinity of imprinted polymers towards the template nonylphenol as compared with blank polymers. The performance of both polymers in solid-phase extraction was however very similar. Both blank and imprinted polymers appeared to be suitable for the removal and pre-concentration of nonylphenol from contaminated water samples with 99% efficiency of the recovery. The commercial resins PH(EC) (Biotage) and C18 (Varian) tested in the same conditions used for comparative purposes had recovery rate <84%. The polymer capacity for nonylphenol was 231 mg g(-1) for blank and 228 mg g(-1) for MIP. The synthesised materials can have significance for sample pre-concentration and environmental analysis of this class of compounds.

  12. Determination of 90Sr by liquid scintillation spectrometry in samples of contaminated water

    International Nuclear Information System (INIS)

    Ometakova, J.; Dulanska, S.

    2009-01-01

    On a model sample we optimized conditions of SPE separation of 90 Sr on Empore Sr Rad Disk in term of use eluent reagent and its appropriate concentration. Also the possibility of multiple use of both sorbents Empore Sr Rad Disk and AnaLig Sr-01 was confirmed. Not even after 8 separations radiochemical yield fall below 87%. For separation of 90 Sr from real sample of percolating water of controlled area of Bohunice NPP three commercially available products were used: 3M Empore Strontium Rad Disk, sorbents AnaLig (with different grain size) and Sr-Resin. The aim of this work was to compare the selected products in term of strontium extracts, the time demandingness and the possibility of multiple use of sorbents. For separation of strontium were also used two classical methods, namely liquid extraction with tributyl phosphate and carbonate precipitation due to the exclusion of interferents. (author)

  13. Cloud point extraction, preconcentration and spectrophotometric determination of nickel in water samples using dimethylglyoxime

    Directory of Open Access Journals (Sweden)

    Morteza Bahram

    2013-01-01

    Full Text Available A new and simple method for the preconcentration and spectrophotometric determination of trace amounts of nickel was developed by cloud point extraction (CPE. In the proposed work, dimethylglyoxime (DMG was used as the chelating agent and Triton X-114 was selected as a non-ionic surfactant for CPE. The parameters affecting the cloud point extraction including the pH of sample solution, concentration of the chelating agent and surfactant, equilibration temperature and time were optimized. Under the optimum conditions, the calibration graph was linear in the range of 10-150 ng mL-1 with a detection limit of 4 ng mL-1. The relative standard deviation for 9 replicates of 100 ng mL-1 Ni(II was 1.04%. The interference effect of some anions and cations was studied. The method was applied to the determination of Ni(II in water samples with satisfactory results.

  14. Description of the U.S. Geological Survey's water-quality sampling and water-level monitoring program at the Hallam Nuclear Facility, August through September 1997

    International Nuclear Information System (INIS)

    1997-01-01

    A water-quality and water-level program between the US Department of Energy (USDOE) and the US Geological Survey (USGS) was re-established in August 1997 to (1) collect one set of water-quality samples from 17 of the 19 USDOE monitor wells, and (2) make five water-level measurements during a 2-month period from the 19 USDOE monitor wells at the Hallam Nuclear Facility, Hallam, Nebraska. Data from these wells are presented

  15. Preparation of water and ice samples for 39Ar dating by atom trap trace analysis (ATTA)

    Science.gov (United States)

    Schwefel, R.; Reichel, T.; Aeschbach-Hertig, W.; Wagenbach, D.

    2012-04-01

    Atom trap trace analysis (ATTA) is a new and promising method to measure very rare noble gas radioisotopes in the environment. The applicability of this method for the dating of very old groundwater with 81Kr has already been demonstrated [1]. Recent developments now show its feasibility also for the analysis of 39Ar [2,3], which is an ideal dating tracer for the age range between 50 and 1000 years. This range is of interest in the fields of hydro(geo)logy, oceanography, and glaciology. We present preparation (gas extraction and Ar separation) methods for groundwater and ice samples for later analysis by the ATTA technique. For groundwater, the sample size is less of a limitation than for applications in oceanography or glaciology. Large samples are furthermore needed to enable a comparison with the classical method of 39Ar detection by low-level counting. Therefore, a system was built that enables gas extraction from several thousand liters of water using membrane contactors. This system provides degassing efficiencies greater than 80 % and has successfully been tested in the field. Gas samples are further processed to separate a pure Ar fraction by a gas-chromatographic method based on Li-LSX zeolite as selective adsorber material at very low temperatures. The gas separation achieved by this system is controlled by a quadrupole mass spectrometer. It has successfully been tested and used on real samples. The separation efficiency was found to be strongly temperature dependent in the range of -118 to -130 °C. Since ATTA should enable the analysis of 39Ar on samples of less than 1 ccSTP of Ar (corresponding to about 100 ml of air, 2.5 l of water or 1 kg of ice), a method to separate Ar from small amounts of gas was developed. Titanium sponge was found to absorb 60 ccSTP of reactive gases per g of the getter material with reasonably high absorption rates at high operating temperatures (~ 800 ° C). Good separation (higher than 92 % Ar content in residual gas) was

  16. Transgenic zebrafish reveal tissue-specific differences in estrogen signaling in response to environmental water samples.

    Science.gov (United States)

    Gorelick, Daniel A; Iwanowicz, Luke R; Hung, Alice L; Blazer, Vicki S; Halpern, Marnie E

    2014-04-01

    Environmental endocrine disruptors (EEDs) are exogenous chemicals that mimic endogenous hormones such as estrogens. Previous studies using a zebrafish transgenic reporter demonstrated that the EEDs bisphenol A and genistein preferentially activate estrogen receptors (ERs) in the larval heart compared with the liver. However, it was not known whether the transgenic zebrafish reporter was sensitive enough to detect estrogens from environmental samples, whether environmental estrogens would exhibit tissue-specific effects similar to those of BPA and genistein, or why some compounds preferentially target receptors in the heart. We tested surface water samples using a transgenic zebrafish reporter with tandem estrogen response elements driving green fluorescent protein expression (5xERE:GFP). Reporter activation was colocalized with tissue-specific expression of ER genes by RNA in situ hybridization. We observed selective patterns of ER activation in transgenic fish exposed to river water samples from the Mid-Atlantic United States, with several samples preferentially activating receptors in embryonic and larval heart valves. We discovered that tissue specificity in ER activation was due to differences in the expression of ER subtypes. ERα was expressed in developing heart valves but not in the liver, whereas ERβ2 had the opposite profile. Accordingly, subtype-specific ER agonists activated the reporter in either the heart valves or the liver. The use of 5xERE:GFP transgenic zebrafish revealed an unexpected tissue-specific difference in the response to environmentally relevant estrogenic compounds. Exposure to estrogenic EEDs in utero was associated with adverse health effects, with the potentially unanticipated consequence of targeting developing heart valves.

  17. The influence of the self-absorption on the measure of the total alpha activity in water samples

    International Nuclear Information System (INIS)

    Acena, M.L.; Gonzalez, J.A.; De Pablo, A.

    1981-01-01

    The self-absorption is an important difficulty in measuring α-activities in river water samples. A semiempirical equation for calculating the self-absorption versus sample thickness has been obtained. This equation is valid for the regular saline residues in spanish rivers and for thicknesses lower than 2 mg x cm -2 . This figure sets a limit for the amount of water to be evaporated from the sample. (author)

  18. UMTRA Project water sampling and analysis plan, Canonsburg, Pennsylvania. Revision 1

    International Nuclear Information System (INIS)

    1995-09-01

    Surface remedial action was completed at the US Department of Energy (DOE) Canonsburg and Burrell Uranium Mill Tailings Remedial Action (UMTRA) Project sites in southwestern Pennsylvania in 1985 and 1987, respectively. The Burrell disposal site, included in the UMTRA Project as a vicinity property, was remediated in conjunction with the remedial action at Canonsburg. On 27 May 1994, the Nuclear Regulatory Commission (NRC) accepted the DOE final Long-Term Surveillance Plan (LTSP) (DOE, 1993) for Burrell thus establishing the site under the general license in 10 CFR section 40.27 (1994). In accordance with the DOE guidance document for long-term surveillance (DOE, 1995), all NRC/DOE interaction on the Burrell site's long-term care now is conducted with the DOE Grand Junction Projects Office in Grand Junction, Colorado, and is no longer the responsibility of the DOE UMTRA Project Team in Albuquerque, New Mexico. Therefore, the planned sampling activities described in this water sampling and analysis plan (WSAP) are limited to the Canonsburg site. This WSAP identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequencies for routine monitoring at the Canonsburg site for calendar years 1995 and 1996. Currently, the analytical data further the site characterization and demonstrate that the disposal cell's initial performance is in accordance with design requirements

  19. Occurrence of pesticides and contaminants of emerging concern in surface waters: Influence of surrounding land use and evaluation of sampling methods

    Science.gov (United States)

    Biologically active compounds originating from agricultural, residential, and industrial sources have been detected in surface waters, which have invoked concern of their potential ecological and human health effects. Automated and grab surface water samples, passive water samples - Polar Organic Co...

  20. Microbial diversity in firework chemical exposed soil and water samples collected in Virudhunagar district, Tamil Nadu, India.

    Science.gov (United States)

    Dhasarathan, P; Theriappan, P; Ashokraja, C

    2010-03-01

    Microbial diversity of soil and water samples collected from pyrochemicals exposed areas of Virdhunagar district (Tamil Nadu, India) was studied. Soil and water samples from cultivable area, waste land and city area of the same region were also studied for a comparative acount. There is a remarkable reduction in total heterotrophic bacterial population (THB) in pyrochemicals exposed soil and water samples (42 × 10(4) CFU/g and 5.6 × 10(4) CFU/ml respectively), compared to the THB of cultivable area soil and water samples (98 × 10(7) CFU/g and 38.6 × 10(7) CFU/ml). The generic composition the THB of the pyrochemicals exposed samples too exhibited considerable change compared to other samples. Pseudomonas sp. was the predominant one (41.6%) followed by Achromobacter sp. (25%) in pyrochemical exposed soil and Pseudomonas sp. was the predominant one (25%) in pyrochemical exposed water samples followed by Bacillus sp. (25%) and Micrococcus sp. (16.6%). It was observed that Cornybacterium sp. and Micrococcus sp. were absent completely in pyrochemical exposed soil and Achromobacter sp. was missing in the pyrochemical exposed water samples, which were present in the other samples. The outcome of this study clearly demonstrates that pollutants such as chemicals used in pyrotechniques affect the microbial biodiversity and suitable measures have to be taken to control the pollution level and to save biodiversity.

  1. Data Validation Package October 2016 Groundwater and Surface Water Sampling at the Monticello, Utah, Disposal and Processing Sites January 2017

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, Jason [USDOE Office of Legacy Management (LM), Washington, DC (United States); Smith, Fred [Navarro Research and Engineering, Inc., Grand Junction, CO (United States)

    2017-02-01

    Sampling Period: October 10–12, 2016. This semiannual event includes sampling groundwater and surface water at the Monticello Disposal and Processing Sites. Sampling and analyses were conducted as specified in the Sampling and Analysis Plan for U.S. Department of Energy Office of Legacy Management Sites (LMS/PRO/S04351, continually updated) and Program Directive MNT-2016-01. Samples were collected from 54 of 64 planned locations (16 of 17 former mill site wells, 15 of 18 downgradient wells, 7 of 9 downgradient permeable reactive barrier wells, 3 of 3 bedrock wells, 4 of 7 seeps and wetlands, and 9 of 10 surface water locations).

  2. Reverse polarity capillary zone electrophoresis analysis of nitrate and nitrite in natural water samples

    Energy Technology Data Exchange (ETDEWEB)

    Metcalf, S.G.

    1998-06-11

    This paper describes the application of reverse polarity capillary zone electrophoresis (RPCE) for rapid and accurate determination of nitrate and nitrite in natural water samples. Using hexamethonium bromide (HMB) as an electroosmotic flow modifier in a borate buffer at pH 9.2, the resolution of nitrate and nitrite was accomplished in less than 3 minutes. RPCE was compared with ion chromatographic (IC) and cadmium reduction flow injection analysis (Cd-FIA) methods which are the two most commonly used standard methods for the analysis of natural water samples for nitrate and nitrite. When compared with the ion chromatographic method for the determination of nitrate and nitrite, RPCE reduced analysis time, decreased detection limits by a factor of 10, cut laboratory wastes by more than two orders of magnitude, and eliminated interferences commonly associated with IC. When compared with the cadmium reduction method, RPCE had the advantage of simultaneous determination of nitrate and nitrite, could be used in the presence of various metallic ions that normally interfere in cadmium reduction, and decreased detection limits by a factor of 10.

  3. A multisyringe flow injection method for the determination of thorium in water samples using spectrophotometric detection

    International Nuclear Information System (INIS)

    Guzman-Mar, J.L.; Aracely Hernandez-Ramirez; Lopez-Chuken, U.J.; Lopez-de-Alba, P.L.; Victor Cerda

    2011-01-01

    A fast and simple multisyringe flow injection analysis (MSFIA) method for routine determination of thorium in water samples was developed. The methodology was based on the complexation reaction of thorium with arsenazo (III) at pH 2.0. Thorium concentrations were spectrophotometrically detected at 665 nm. Under optimal conditions, Beer's law was obeyed over the range from 0.2 to 4.5 μg mL -1 thorium, a 3σ detection limit of 0.05 μg mL -1 , and a 10σ quantification limit of 0.2 μg mL -1 were obtained. The relative standard deviations (RSD, %) at 0.5, 2.5 and 4.5 μg mL -1 was 2.8, 1.5 and 0.8%, respectively (n = 10). It was found that most of the common metal ions and anions did not interfere with the thorium determination. The proposed method was successfully applied to its analysis in various water samples. (author)

  4. Quality demonstration of analytica procedure for quantification of 134Cesium and 137Cesium in water samples

    International Nuclear Information System (INIS)

    Santos, T.O.; Farias, E.E.G.; Filho, C.A.S.; França, E.J. de

    2017-01-01

    Intercomparison programs are extremely important in attesting the metrological quality of laboratories, contributing to the improvement of the quality of the analytical procedures adopted and the validation of new analytical methodologies. The objective of this work is to demonstrate the quality of the analyzes of radionuclides Cs-134 and Cs-137 by High Resolution Gamma Spectrometry in water samples of the PNI (National Intercomparison Program). Prior to the start of the analyzes, the vials containing the concentrated samples are shaken for about 10 minutes to ensure homogeneity. A 500 ml aliquot of the concentrated solution is transferred to a beaker for dilution with 1% (v / v) HNO 3 to 4 liters. After being shaken for 30 minutes, 2 liters of this diluted solution are transferred to a Marinelli vessel and then analyzed by High Resolution Gamma Spectrometry (EGAR) using germanium Hyperpure-HPGe detectors. The results obtained are reported to the IRD for analytical performance evaluation. Based on the intercomparison rounds as of year 2011, the SEAMB/CRCN/NE (Environmental Monitoring Service of the Regional Center of Nuclear Sciences of the Northeast) participated in eight rounds of the PNI. All results were within the range of standard deviation evaluation parameter calculated by the IRD. The results obtained demonstrate the analytical capacity of the CRCN-NE for radiometric analyzes in water

  5. A nanosilver-based spectrophotometric method for determination of malachite green in surface water samples.

    Science.gov (United States)

    Sahraei, R; Farmany, A; Mortazavi, S S; Noorizadeh, H

    2013-07-01

    A new spectrophotometric method is reported for the determination of nanomolar level of malachite green in surface water samples. The method is based on the catalytic effect of silver nanoparticles on the oxidation of malachite green by hexacyanoferrate (III) in acetate-acetic acid medium. The absorbance is measured at 610 nm with the fixed-time method. Under the optimum conditions, the linear range was 8.0 × 10(-9)-2.0 × 10(-7) mol L(-1) malachite green with a correlation coefficient of 0.996. The limit of detection (S/N = 3) was 2.0 × 10(-9) mol L(-1). Relative standard deviation for ten replicate determinations of 1.0 × 10(-8) mol L(-1) malachite green was 1.86%. The method is featured with good accuracy and reproducibility for malachite green determination in surface water samples without any pre-concentration and separation step.

  6. Electrochemical detection of a powerful estrogenic endocrine disruptor: ethinylestradiol in water samples through bioseparation procedure.

    Science.gov (United States)

    Martínez, Noelia A; Pereira, Sirley V; Bertolino, Franco A; Schneider, Rudolf J; Messina, Germán A; Raba, Julio

    2012-04-20

    The synthetic estrogen ethinylestradiol (EE2) is an active component of oral contraceptives (OCs), considered as an endocrine disrupting compound (EDC). It is excreted from humans and released via sewage treatment plant effluents into aquatic environments. EDCs are any environmental pollutant chemical that, once incorporated into an organism, affects the hormonal balance of various species including humans. Its presence in the environment is becoming of great importance in water quality. This paper describes the development of an accurate, sensitive and selective method for capture, preconcentration and determination of EE2 present in water samples using: magnetic particles (MPs) as bioaffinity support for the capture and preconcentration of EE2 and a glassy carbon electrode modified with multi-walled carbon nanotubes (MWCNTs/GCE) as detection system. The capture procedure was based on the principle of immunoaffinity, the EE2 being extracted from the sample using the anti-EE2 antibodies (anti-EE2 Ab) which were previously immobilized on MPs. Subsequently the analyte desorption was done employing a sulfuric acid solution and the determination of the EE2 in the pre-concentrated solution was carried out by square wave voltammetry (SWV). This method can be used to determine EE2 in the range of 0.035-70 ng L(-1) with a detection limit (LOD) of 0.01 ng L(-1) and R.S.D.levels. Copyright © 2012 Elsevier B.V. All rights reserved.

  7. Reverse polarity capillary zone electrophoresis analysis of nitrate and nitrite in natural water samples

    International Nuclear Information System (INIS)

    Metcalf, S.G.

    1998-01-01

    This paper describes the application of reverse polarity capillary zone electrophoresis (RPCE) for rapid and accurate determination of nitrate and nitrite in natural water samples. Using hexamethonium bromide (HMB) as an electroosmotic flow modifier in a borate buffer at pH 9.2, the resolution of nitrate and nitrite was accomplished in less than 3 minutes. RPCE was compared with ion chromatographic (IC) and cadmium reduction flow injection analysis (Cd-FIA) methods which are the two most commonly used standard methods for the analysis of natural water samples for nitrate and nitrite. When compared with the ion chromatographic method for the determination of nitrate and nitrite, RPCE reduced analysis time, decreased detection limits by a factor of 10, cut laboratory wastes by more than two orders of magnitude, and eliminated interferences commonly associated with IC. When compared with the cadmium reduction method, RPCE had the advantage of simultaneous determination of nitrate and nitrite, could be used in the presence of various metallic ions that normally interfere in cadmium reduction, and decreased detection limits by a factor of 10

  8. Determination of the uranium concentration in water samples by the technique of fission track recording

    International Nuclear Information System (INIS)

    Geraldo, L.P.

    1979-01-01

    The technique of fission track register was developed for the determination of micrograms of uranium. The Makrofol KG, a synthetic plastic made by Bayer, was used as the detector and the wet method was utilized. The detector calibration curve allows the determination of the uranium concentration in a sample within an interval from 8.0 to 0.4μgU/L, the total error ranging from 3.3% to 29.0% respectively. The method was used in the determination of the uranium content in various water samples, obtained from various sources like rivers, sea etc. in the state of Sao Paulo, Brazil. Results were compared with those obtained by other authors using different methods. The average concentration found in sea waters (3.27 +- 9.12μgU/l) by this method is compatible with the international average accepted value of 3.3μgU/l, irrespective of site and depth. The determination of the uranium content by fission track counting has proved to be very convenient. (Author) [pt

  9. The correlation of arsenic levels in drinking water with the biological samples of skin disorders

    International Nuclear Information System (INIS)

    Kazi, Tasneem Gul; Arain, Muhammad Balal; Baig, Jameel Ahmed; Jamali, Muhammad Khan; Afridi, Hassan Imran; Jalbani, Nusrat; Sarfraz, Raja Adil; Shah, Abdul Qadir; Niaz, Abdul

    2009-01-01

    Arsenic (As) poisoning has become a worldwide public health concern. The skin is quite sensitive to As and skin lesions are the most common and earliest nonmalignant effects associated to chronic As exposure. In 2005-2007, a survey was carried out on surface and groundwater arsenic contamination and relationships between As exposure via the drinking water and related adverse health effects (melanosis and keratosis) on villagers resides on the banks of Manchar lake, southern part of Sindh, Pakistan. We screened the population from arsenic-affected villages, 61 to 73% population were identified patients suffering from chronic arsenic toxicity. The effects of As toxicity via drinking water were estimated by biological samples (scalp hair and blood) of adults (males and females), have or have not skin problem (n = 187). The referent samples of both genders were also collected from the areas having low level of As ( 2 = 0.852 and 0.718) as compared to non-diseased subjects (R 2 = 0.573 and 0.351), respectively

  10. Ionic liquid-based dispersive microextraction of nitro toluenes in water samples

    International Nuclear Information System (INIS)

    Berton, Paula; Regmi, Bishnu P.; Spivak, David A.; Warner, Isiah M.

    2014-01-01

    We describe a method for dispersive liquid-liquid microextraction of nitrotoluene-based compounds. This method is based on use of the room temperature ionic liquid (RTIL) 1-hexyl-4-methylpyridinium bis(trifluoromethylsulfonyl)imide as the accepting phase, and is shown to work well for extraction of 4-nitrotoluene, 2,4-dinitrotoluene, and 2,4,6-trinitrotoluene. Separation and subsequent detection of analytes were accomplished via HPLC with UV detection. Several parameters that influence the efficiency of the extraction were optimized using experimental design. In this regard, a Plackett–Burman design was used for initial screening, followed by a central composite design to further optimize the influencing variables. For a 5-mL water sample, the optimized IL-DLLME procedure requires 26 mg of the RTIL as extraction solvent and 680 μL of methanol as the dispersant. Under optimum conditions, limits of detection (LODs) are lower than 1.05 μg L −1 . Relative standard deviations for 6 replicate determinations at a 4 μg L −1 analyte level are <4.3 % (calculated using peak areas). Correlation coefficients of >0.998 were achieved. This method was successfully applied to extraction and determination of nitrotoluene-based compounds in spiked tap and lake water samples. (author)

  11. Analytical strategies for uranium determination in natural water and industrial effluents samples

    International Nuclear Information System (INIS)

    Santos, Juracir Silva

    2011-01-01

    The work was developed under the project 993/2007 - 'Development of analytical strategies for uranium determination in environmental and industrial samples - Environmental monitoring in the Caetite city, Bahia, Brazil' and made possible through a partnership established between Universidade Federal da Bahia and the Comissao Nacional de Energia Nuclear. Strategies were developed to uranium determination in natural water and effluents of uranium mine. The first one was a critical evaluation of the determination of uranium by inductively coupled plasma optical emission spectrometry (ICP OES) performed using factorial and Doehlert designs involving the factors: acid concentration, radio frequency power and nebuliser gas flow rate. Five emission lines were simultaneously studied (namely: 367.007, 385.464, 385.957, 386.592 and 409.013 nm), in the presence of HN0 3 , H 3 C 2 00H or HCI. The determinations in HN0 3 medium were the most sensitive. Among the factors studied, the gas flow rate was the most significant for the five emission lines. Calcium caused interference in the emission intensity for some lines and iron did not interfere (at least up to 10 mg L -1 ) in the five lines studied. The presence of 13 other elements did not affect the emission intensity of uranium for the lines chosen. The optimized method, using the line at 385.957 nm, allows the determination of uranium with limit of quantification of 30 μg L -1 and precision expressed as RSD lower than 2.2% for uranium concentrations of either 500 and 1000 μg L -1 . In second one, a highly sensitive flow-based procedure for uranium determination in natural waters is described. A 100-cm optical path flow cell based on a liquid-core waveguide (LCW) was exploited to increase sensitivity of the arsenazo 111 method, aiming to achieve the limits established by environmental regulations. The flow system was designed with solenoid micro-pumps in order to improve mixing and minimize reagent consumption, as well as

  12. Correlation of Heavy Element in Sea Water and Sediment Samples from Peninsula of Muria

    International Nuclear Information System (INIS)

    Rosidi; Sukirno

    2007-01-01

    The analysis of heavy metals in marine environmental samples peninsula of Muria in the year 2004 has been carried out by using neutron activation analysis (NAA) method. The objective of this analysis is to know the distribution of heavy metals in the sea water and sediment, which accommodate the recent environmental data in supporting the license of site for the nuclear power plants (NPP). The result of the analysis show that there were only 5 observed elements found in sea water and sediment were Cd, Co, Cr, Sb and Sc. All of heavy metals from sea water (0.002 mg/l) are obviously lower than the threshold value established by environmental minister Act; Kep LH No 51/2004. From the observed data to use software of SPSS version 10, application of the Pearson correlation (r) shows that between Co with Sc was indicator show a highly positive significant correlation (r=0.928), between Cr with Sc was sufficiently positive high (r=0.756), between Cr with Cd was precisely (r=0.611) while Co with Sb shows the significantly low (r=0.429). (author)

  13. Method to determine trace elements in water samples by neutron activation analysis

    International Nuclear Information System (INIS)

    Kueppers, G.; Erdtmann, G.

    1981-05-01

    For the determination of trace elements in water by neutron activation analysis irradiation porcedures and chemical separation procedures have been developed. Irradiation in melted quarz glass ampoules in the presence of a platinum wire (for recombination of the oxyhydrogen gas produced by radiolysis) proved successfull with different variants of the irradiation methods, as long irradiation periods without pressure build-up could be achieved. Possible falsifications of the analysis results were investigated in detail (losses by absorption on vessel walls etc.). The irradiated samples can be measured directly with a gamma ray spectrometer and from the radionuclides found the trace element contents may be calculated. More sensitive determinations are possible if the radionuclides are chemically separated. Procedures for removing the matrix activities, for the separation of the radionuclides in groups of elements and for the isolation of single elements have been developed. For especially sensitive determination of some elements selective separation procedures for antimony, cadmium, selenium, mercury and uranium have been developed. The analytical procedures described have been applied to trace element determinations in river water, glacier ice and water solutions from technical processes. (orig./RB) [de

  14. Water quality monitoring: A comparative case study of municipal and Curtin Sarawak's lake samples

    International Nuclear Information System (INIS)

    Kumar, A Anand; Prabakaran, K; Nagarajan, R; Jaison, J; Chan, Y S

    2016-01-01

    In this study, particle size distribution and zeta potential of the suspended particles in municipal water and lake surface water of Curtin Sarawak's lake were compared and the samples were analysed using dynamic light scattering method. High concentration of suspended particles affects the water quality as well as suppresses the aquatic photosynthetic systems. A new approach has been carried out in the current work to determine the particle size distribution and zeta potential of the suspended particles present in the water samples. The results for the lake samples showed that the particle size ranges from 180nm to 1345nm and the zeta potential values ranges from -8.58 mV to -26.1 mV. High zeta potential value was observed in the surface water samples of Curtin Sarawak's lake compared to the municipal water. The zeta potential values represent that the suspended particles are stable and chances of agglomeration is lower in lake water samples. Moreover, the effects of physico-chemical parameters on zeta potential of the water samples were also discussed. (paper)

  15. Porphyrin-based magnetic nanocomposites for efficient extraction of polycyclic aromatic hydrocarbons from water samples.

    Science.gov (United States)

    Yu, Jing; Zhu, Shukui; Pang, Liling; Chen, Pin; Zhu, Gang-Tian

    2018-03-09

    Stable and reusable porphyrin-based magnetic nanocomposites were successfully synthesized for efficient extraction of polycyclic aromatic hydrocarbons (PAHs) from environmental water samples. Meso-Tetra (4-carboxyphenyl) porphyrin (TCPP), a kind of porphyrin, can connect the copolymer after amidation and was linked to Fe 3 O 4 @SiO 2 magnetic nanospheres via cross-coupling. Several characteristic techniques such as field emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectrometry, vibrating sample magnetometry and a tensiometer were used to characterize the as-synthesized materials. The structure of the copolymer was similar to that of graphene, possessing sp 2 -conjugated carbon rings, but with an appropriate amount of delocalized π-electrons giving rise to the higher extraction efficiency for heavy PAHs without sacrificing the performance in the extraction of light PAHs. Six extraction parameters, including the TCPP:Fe 3 O 4 @SiO 2 (m:m) ratio, the amount of adsorbents, the type of desorption solvent, the desorption solvent volume, the adsorption time and the desorption time, were investigated. After the optimization of extraction conditions, a comparison of the extraction efficiency of Fe 3 O 4 @SiO 2 -TCPP and Fe 3 O 4 @SiO 2 @GO was carried out. The adsorption mechanism of TCPP to PAHs was studied by first-principles density functional theory (DFT) calculations. Combining experimental and calculated results, it was shown that the π-π stacking interaction was the main adsorption mechanism of TCPP for PAHs and that the amount of delocalized π-electrons plays an important role in the elution process. Under the optimal conditions, Fe 3 O 4 @SiO 2 -porphyrin showed good precision in intra-day (<8.9%) and inter-day (<13.0%) detection, low method detection limits (2-10 ng L -1 ), and wide linearity (10-10000 ng L -1 ). The method was applied to simultaneous analysis of 15 PAHs with

  16. Highly efficient detection of paclobutrazol in environmental water and soil samples by time-resolved fluoroimmunoassay

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Zhenjiang, E-mail: lzj1984@ujs.edu.cn [School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013 (China); Wei, Xi [School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013 (China); The Affiliated First People' s Hospital of Jiangsu University, Zhenjiang 212002 (China); Ren, Kewei; Zhu, Gangbing; Zhang, Zhen; Wang, Jiagao; Du, Daolin [School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013 (China)

    2016-11-01

    A fast and ultrasensitive indirect competitive time-resolved fluoroimmunoassay (TRFIA) was developed for the analysis of paclobutrazol in environmental water and soil samples. Paclobutrazol hapten was synthesized and conjugated to bovine serum albumin (BSA) for producing polyclonal antibodies. Under optimal conditions, the 50% inhibitory concentration (IC{sub 50} value) and limit of detection (LOD, IC{sub 20} value) were 1.09 μg L{sup −} {sup 1} and 0.067 μg L{sup −} {sup 1}, respectively. The LOD of TRFIA was improved 30-fold compared to the already reported ELISA. There was almost no cross-reactivity of the antibody with the other structural analogues of triazole compounds, indicating that the antibody had high specificity. The average recoveries from spiked samples were in the range from 80.2% to 104.7% with a relative standard deviation of 1.0–9.5%. The TRFIA results for the real samples were in good agreement with that obtained by high-performance liquid chromatography analyses. The results indicate that the established TRFIA has potential application for screening paclobutrazol in environmental samples. - Highlights: • The approach to design and synthesize the PBZ hapten was more straightforward. • A rapid and ultrasensitive TRFIA was developed and applied to the screening of PBZ. • The TRFIA for real soil samples showed reliability and high correlation with HPLC. • The PBZ TRFIA showed high sensitivity, simple operation, a wide range of quantitative analyses and no radioactive hazards.

  17. Zirconium(IV) functionalized magnetic nanocomposites for extraction of organophosphorus pesticides from environmental water samples.

    Science.gov (United States)

    Jiang, Li; Huang, Tengjun; Feng, Shun; Wang, Jide

    2016-07-22

    The widespread use of organophosphate pesticides (OPPs) in agriculture leads to residue accumulation in the environment which is dangerous to human health and disrupts the ecological balance. In this work, one nanocomposite immobilized zirconium (Zr, IV) was prepared and used as the affinity probes to quickly and selectively extract organophosphorus pesticides (OPPs) from water samples. The Fe3O4-ethylenediamine tetraacetic acid (EDTA)@Zr(IV) nanocomposites (NPs) were prepared by simply mixing Zr(IV) ions with Fe3O4-EDTA NPs synthesized by one-pot chemical co-precipitation method. The immobilized Zr(IV) ions were further utilized to capture OPPs based on their high affinity for the phosphate moiety in OPPs. Coupled with GC-MS, four OPPs were used as models to demonstrate the feasibility of this approach. Under the optimum conditions, the limits of detection for target OPPs were in the range of 0.10-10.30ngmL(-1) with relative standard deviations (RSDs) of 0.61-4.40% (n=3), respectively. The linear ranges were over three orders of magnitudes (correlation coefficients, R(2)>0.9995). The Fe3O4-EDTA@Zr(IV) NPs were successfully applied to extract OPPs samples with recoveries of 86.95-112.60% and RSDs of 1.20-10.42% (n=3) from two spiked real water. By the proposed method, the matrix interference could be effectively eliminated. We hope our finding can provide a promising alternative for the fast extraction of OPPs from complex real samples. Copyright © 2016 Elsevier B.V. All rights reserved.

  18. Use of graphene supported on aminopropyl silica for microextraction of parabens from water samples.

    Science.gov (United States)

    Fumes, Bruno Henrique; Lanças, Fernando Mauro

    2017-03-03

    This paper describes the synthesis, characterization and use of graphene supported on aminopropyl silica through covalent bonds (Si-G) as a sorbent for microextraction by packed sorbent (MEPS). Five parabens (methyl, ethyl, propyl, butyl and benzyl) present in water matrices were used as model compounds for this evaluation. The Si-G phase was compared to other sorbents used in MEPS (C18 and Strata™-X) and also with graphene supported on primary-secondary amine (PSA) silica, where Si-G showed better results. After this, the MEPS experimental parameters were optimized using the Si-G sorbent. The following variables were optimized through univariate experiments: pH (4,7 and 10), desorption solvent (ACN:MeOH (50:50), ACN:H 2 O (40:60), MeOH and ACN) and ionic strength (0, 10 and 20% of NaCl). A factorial design 2 6-2 was then employed to evaluate other variables, such as the sample volume, desorption volume, sampling cycles, wash cycles and desorption cycles, as well as the influence of NaCl% on the extraction performance. The optimized method achieved a linear range of 0.2-20μg/L for most parabens; weighted calibration models were employed during the linearity evaluation to reduce the absolute sum of the residue values and improve R 2 , which ranged from 0.9753 to 0.9849. The method's accuracy was 82.3-119.2%; precision, evaluated as the coefficient of variance for intraday and interday analysis, ranged from 1.5 to 19.2%. After evaluation of the figures of merit, the method was applied to the determination of parabens in water samples. Copyright © 2017 Elsevier B.V. All rights reserved.

  19. Evaluation of the toxicological properties of ground- and surface-water samples from the Aral Sea Basin

    International Nuclear Information System (INIS)

    Bosch, K.; Erdinger, L.; Ingel, F.; Khussainova, S.; Utegenova, E.; Bresgen, N.; Eckl, P.M.

    2007-01-01

    In order to determine whether there is a potential health risk associated with the water supply in the Aral Sea Basin, ground- and surface-water samples were collected in and around Aralsk and from the Aral Sea in 2002. Water samples from Akchi, a small town close to Almaty, served as controls. Bioassays with different toxicological endpoints were employed to assess the general toxicological status. Additionally, the samples were analysed for microbial contamination. The samples were tested in the primary hepatocyte assay for their potential to induce micronuclei and chromosomal aberrations as cumulative indicators for genotoxicity. In parallel, the effects on cell proliferation evidenced by mitotic index and cytotoxicity such as the appearance of necrotic and apoptotic cells, were determined. Furthermore, samples were examined using the Microtox assay for general toxicity. Chemical analysis according to European regulations was performed and soil and water samples were analysed for DDT and DDE. The results obtained indicated no increased cyto- or genotoxic potential of the water samples, nor levels of DDT or DDE exceeding the thresholds levels suggested by WHO. Our data therefore do not support the hypothesis that the contamination of the drinking water in and around Aralsk is responsible for the health effects previously described such as increased rates of liver disease and in particular liver cancer. Microbiological analysis, however, revealed the presence of contamination in most samples analysed

  20. [Monitoring microbiological safety of small systems of water distribution. Comparison of two sampling programs in a town in central Italy].

    Science.gov (United States)

    Papini, Paolo; Faustini, Annunziata; Manganello, Rosa; Borzacchi, Giancarlo; Spera, Domenico; Perucci, Carlo A

    2005-01-01

    To determine the frequency of sampling in small water distribution systems (distribution. We carried out two sampling programs to monitor the water distribution system in a town in Central Italy between July and September 1992; the Poisson distribution assumption implied 4 water samples, the assumption of negative binomial distribution implied 21 samples. Coliform organisms were used as indicators of water safety. The network consisted of two pipe rings and two wells fed by the same water source. The number of summer customers varied considerably from 3,000 to 20,000. The mean density was 2.33 coliforms/100 ml (sd= 5.29) for 21 samples and 3 coliforms/100 ml (sd= 6) for four samples. However the hypothesis of homogeneity was rejected (p-value samples (beta= 0.24) than with 21 (beta= 0.05). For this small network, determining the samples' size according to heterogeneity hypothesis strengthens the statement that water is drinkable compared with homogeneity assumption.

  1. Application of an immobilized ionic liquid for the passive sampling of perfluorinated substances in water.

    Science.gov (United States)

    Wang, Lei; Gong, Xinying; Wang, Ruonan; Gan, Zhiwei; Lu, Yuan; Sun, Hongwen

    2017-09-15

    Ionic liquids have been used to efficiently extract a wide range of polar and nonpolar organic contaminants from water. In this study, imidazole ionic liquids immobilized on silica gel were synthesized through a chemical bonding method, and the immobilized dodecylimidazolium ionic liquid was selected as the receiving phase material in a POCIS (polar organic chemical integrative sampler) like passive sampler to monitor five perfluoroalkyl substances (PFASs) in water. Twenty-one days of integrative accumulation was conducted in laboratory scale experiments, and the accumulated PFASs in the samplers were eluted and analyzed by high performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS). The partitioning coefficients of most PFASs between sampler sorbents and water in the immobilized ionic liquid (IIL)-sampler were higher than those in the HLB-sampler, especially for compounds with shorter alkyl chains. The effects of flow velocity, temperature, dissolved organic matter (DOM) and pH on the uptake of these analytes were also evaluated. Under the experimental conditions, the uptake of PFASs in the IIL-sampler slightly increased with the flow velocity and temperature, while different influences of DOM and pH on the uptake of PFAS homologues with short or long chains were observed. The designed IIL-samplers were applied in the influent and effluent of a wastewater treatment plant. All five PFASs could be accumulated in the samplers, with concentrations ranging from 6.5×10 -3 -3.6×10 -1 nmol/L in the influent and from 1.3×10 -2 -2.2×10 -1 nmol/L in the effluent. The calculated time-weighted average concentrations of most PFASs fit well with the detected concentrations of the active sampling, indicating the applicability of the IIL-sampler in monitoring these compounds in water. Copyright © 2017 Elsevier B.V. All rights reserved.

  2. Analysis of nitrates and nitrites in subsoil and ground water samples in Swaziland

    Directory of Open Access Journals (Sweden)

    A.O. Fadiran

    2005-06-01

    Full Text Available The concentrations of nitrate as nitrogen (NO3–N in mg/L and nitrite as nitrogen (NO2–N in µg/L were determined in water samples from 60 boreholes, 21 shallow wells and 7 springs located in the four regions of the country. For all the 88 sampling points nitrate levels vary within 0.05 plus or minus 0.00 – 28.44 plus or minus 0.80 mg/L NO3–N, out of which 10.22% have mg/L NO3–N ≥ MCL (maximum contaminant level of 10 mg/L NO3–N. Shallow wells recorded the highest NO3–N% ≥ MCL of 20.0% followed by boreholes with NO3–N % ≥ MCL of 8.33% while for springs, the NO3–N % ≥ MCL was zero. On the other hand, NO2–N (μg/L from all the sampling points vary within (ND/0.30 plus or minus 0.00 – 297.0 plus or minus 0.50 μg/L NO2–N, which were far below the recommended MCL of 1 mg/L (= 1000 μg/L.

  3. A high precision mass spectrometer for hydrogen isotopic analysis of water samples

    International Nuclear Information System (INIS)

    Murthy, M.S.; Prahallada Rao, B.S.; Handu, V.K.; Satam, J.V.

    1979-01-01

    A high precision mass spectrometer with two ion collector assemblies and direct on line reduction facility (with uranium at 700 0 C) for water samples for hydrogen isotopic analysis has been designed and developed. The ion source particularly gives high sensitivity and at the same tike limits the H 3 + ions to a minimum. A digital ratiometer with a H 2 + compensator has also been developed. The overall precision obtained on the spectrometer is 0.07% 2sub(sigmasub(10)) value. Typical results on the performance of the spectrometer, which is working since a year and a half are given. Possible methods of extending the ranges of concentration the spectrometer can handle, both on lower and higher sides are discussed. Problems of memory between samples are briefly listed. A multiple inlet system to overcome these problems is suggested. This will also enable faster analysis when samples of highly varying concentrations are to be analyzed. A few probable areas in which the spectrometer will be shortly put to use are given. (auth.)

  4. Site-Wide Integrated Water Monitoring - Defining and Implementing Sampling Objectives to Support Site Closure - 13060

    International Nuclear Information System (INIS)

    Wilborn, Bill; Knapp, Kathryn; Farnham, Irene; Marutzky, Sam

    2013-01-01

    The Underground Test Area (UGTA) activity is responsible for assessing and evaluating the effects of the underground nuclear weapons tests on groundwater at the Nevada National Security Site (NNSS), formerly the Nevada Test Site (NTS), and implementing a corrective action closure strategy. The UGTA strategy is based on a combination of characterization, modeling studies, monitoring, and institutional controls (i.e., monitored natural attenuation). The closure strategy verifies through appropriate monitoring activities that contaminants of concern do not exceed the SDWA at the regulatory boundary and that adequate institutional controls are established and administered to ensure protection of the public. Other programs conducted at the NNSS supporting the environmental mission include the Routine Radiological Environmental Monitoring Program (RREMP), Waste Management, and the Infrastructure Program. Given the current programmatic and operational demands for various water-monitoring activities at the same locations, and the ever-increasing resource challenges, cooperative and collaborative approaches to conducting the work are necessary. For this reason, an integrated sampling plan is being developed by the UGTA activity to define sampling and analysis objectives, reduce duplication, eliminate unnecessary activities, and minimize costs. The sampling plan will ensure the right data sets are developed to support closure and efficient transition to long-term monitoring. The plan will include an integrated reporting mechanism for communicating results and integrating process improvements within the UGTA activity as well as between other U.S. Department of Energy (DOE) Programs. (authors)

  5. Microbial Safety of Low Water Activity Foods: Study of Simulated and Durban Household Samples

    Directory of Open Access Journals (Sweden)

    O. A. Ijabadeniyi

    2017-01-01

    Full Text Available Sixty household low water activity foods were examined and a simulative study was conducted in a high sugar, low aw almond and macadamia butter to determine the survival of Bacillus cereus and Staphylococcus aureus ATCC 25923. Results obtained from 60 low aw samples collected at household level had some significant differences (P≤0,05 within food categories amongst the various tests. Spices had the highest number of aerobic bacteria, aerobic spore-formers, anaerobic spore-formers, and S. aureus. Mean aerobic colony counts for nuts and spices were 2.30 log CFU/g and 4.40 log CFU/g, respectively. Pathogens such as Escherichia coli and Cronobacter sakazakii were present in nuts, whilst Salmonella spp. was present in chocolates. This implies that certain low aw foods may present a public health risk. In the simulative study, temperature and high sucrose concentrations played a significant role in the survival of B. cereus and S. aureus ATCC 25923. B. cereus was found to be more osmotolerant at both reduced and elevated temperatures (18°C and 25°C in the 12% sucrose sample in both butters, whilst S. aureus ATCC 25923 seemed to grow better in sucrose-free samples at both temperatures in both butters. This implies that certain low aw foods may present a public health risk. Also, B. cereus, being a spore-forming bacterium, can be osmotolerant at both reduced and elevated temperatures.

  6. Determination methods of the 90Sr in a sample of contaminated water

    International Nuclear Information System (INIS)

    Ometakova, J.; Silvia Dulanska, S.

    2009-01-01

    The aim of this work was a comparison of selected products from the point of view of the amount of strontium yields, time needed and possibility of multiple use of sorbents. Three commercial products: 3M Empore Stroncium Rad Disk, AnaLig , Sr-Resin and two classical methods: liquid-liquid extraction with tributylphosphate and carbonate coprecipitation (to eliminate interferents) were used for separation of 90 Sr. The model sample was used in radiochemical analysis to check multiple use of 3M Em-pore Stroncium Rad Disk a AnaLig. A radiochemical strontium yield was traced by using radionuclide 85 Sr. The model sample was also used to optimize conditions of strontium separation. The results were used for 90 Sr determination from a sample of permeating groundwater from a supervised zone of a Nuclear Power Plant Jaslovske Bohunice. We have found out that 90 Sr separation with sorbents AnaLig Sr-01, 3M Empore Sr Rad Disk is as effective as with sorbent Sr-Resin in matrices of contaminated water. (authors)

  7. Radiological assessment of coastal marine sediment and water samples, Karachi coast, Pakistan

    International Nuclear Information System (INIS)

    Qureshi, R.M.; Mashiatullah, A.; Akram, M.; Sajjad, M.I.; Shafiq, M.; Javed, T.; Aslam, M.

    1999-04-01

    Concentrations of selective natural radionuclides (/sup 226/Ra, /sup 228/Ra, /sup 40/K) in shallow marine coastal sediments and sea water off Karachi coast, Pakistan, were measured with a hyper pure germanium (HPGe) gamma spectrometer. Sediment and water samples were collected from polluted Layari and Malire River downstream (pre-out fall), Gizri Creek, Layari River out fall in Karachi harbor, Karachi Harbor/ Manora Channel Mains, as well as from open sea (South-East Coast and North-West Coast) within the 10m depth contour. No artificial radionuclides (e.g. /sup 60/Co, /sup 137/Cs and /sup 134/Cs were detected in both water and sediment samples at any of these locations. The activity of /sup 226/Ra in coastal river sediments is found below its limit of detection (<18.35 Bqkg/sup -1/). Activity of /sup 228/Ra in sediments off Karachi Coast ranges between 11.80 +- 3.60 to 37.27+- 4.31 Bqkg/sup -1/. The highest activity was found south of Nuclear Power Station (KANUPP) and the lowest activity was found in the vicinity of Oyster Rocks (open sea). The /sup 226/Ra activity ranges from 19.40+- 5.88 to 67.14 +- 10.02 Bqkg/sup -1/. The activity of /sup 228/Ra in sediments of Manora Channel, South-east Coast of Karachi and the North west coast of Karachi are also in agreement with the IAEA marine sediment standard namely: IAEA-135 (/sup 228/Ra = 36.7 +- 3 Bqkg/sup -1/). The activity of /sup 226/Ra for the South East Coast of Karachi and the North west coast of Karachi are also in agreement with the IAEA marine sediment standard namely: IAEA 135(/sup 226/Ra=23.9 +- 1.1 Bqkg/sup -1/) and Pacific Ocean sediment standard namely: IAEA-368 (/sup 226/Ra=21.4+- 1.1 Bqkg/sup -1/). The /sup 40/K activity in sea sediments varies from 197.7+- 44.24 to 941.90 +- 39.00 Bqkg-1). The highest activity is observed in the vicinity of Oyster Rocks (open sea) along the Clifton coast (South-East Cost of Karachi) and the lowest activity is found south of Nuclear Power Station (KANUPP) along the

  8. Measurement of extremely (2) H-enriched water samples by laser spectrometry: application to batch electrolytic concentration of environmental tritium samples.

    Science.gov (United States)

    Wassenaar, L I; Kumar, B; Douence, C; Belachew, D L; Aggarwal, P K

    2016-02-15

    Natural water samples artificially or experimentally enriched in deuterium ((2) H) at concentrations up to 10,000 ppm are required for various medical, environmental and hydrological tracer applications, but are difficult to measure using conventional stable isotope ratio mass spectrometry. Here we demonstrate that off-axis integrated cavity output (OA-ICOS) laser spectrometry, along with (2) H-enriched laboratory calibration standards and appropriate analysis templates, allows for low-cost, fast, and accurate determinations of water samples having δ(2) HVSMOW-SLAP values up to at least 57,000 ‰ (~9000 ppm) at a processing rate of 60 samples per day. As one practical application, extremely (2) H-enriched samples were measured by laser spectrometry and compared to the traditional (3) H Spike-Proxy method in order to determine tritium enrichment factors in the batch electrolysis of environmental waters. Highly (2) H-enriched samples were taken from different sets of electrolytically concentrated standards and low-level (tritium samples, and all cases returned accurate and precise initial low-level (3) H results. The ability to quickly and accurately measure extremely (2) H-enriched waters by laser spectrometry will facilitate the use of deuterium as a tracer in numerous environmental and other applications. For low-level tritium operations, this new analytical ability facilitated a 10-20 % increase in sample productivity through the elimination of spike standards and gravimetrics, and provides immediate feedback on electrolytic enrichment cell performance. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

  9. Area G perimeter surface-soil and single-stage water sampling. Environmental surveillance for fiscal year 95. Progress report

    International Nuclear Information System (INIS)

    Childs, M.; Conrad, R.

    1997-09-01

    ESH-19 personnel collected soil and single-stage water samples around the perimeter of Area G at Los Alamos National Laboratory (LANL) during FY 95 to characterize possible radionuclide movement out of Area G through surface water and entrained sediment runoff. Soil samples were analyzed for tritium, total uranium, isotopic plutonium, americium-241, and cesium-137. The single-stage water samples were analyzed for tritium and plutonium isotopes. All radiochemical data was compared with analogous samples collected during FY 93 and 94 and reported in LA-12986 and LA-13165-PR. Six surface soils were also submitted for metal analyses. These data were included with similar data generated for soil samples collected during FY 94 and compared with metals in background samples collected at the Area G expansion area

  10. Radiation dose due to radon and heavy metal analysis in drinking water samples of Jammu district, J. and K., India

    International Nuclear Information System (INIS)

    Ajay Kumar; Kaur, Manpreet; Sharma, Sumit; Mehra, Rohit; Sharma, Dinesh Kumar

    2015-01-01

    The aim of this study is to determine the relationship between the contaminant drinking water and its impact on human health. The most contaminants of ground water are heavy metals like arsenic, cadmium, mercury, copper, zinc and etc. These heavy metals particularly cause strong toxicity even at low concentration. Heavy metals are considered to be the major pollutants of water sources. Heavy metal toxicity can result in damaged or reduced mental and central nervous function, lower energy levels and damage to blood composition, lungs, kidneys, liver and other vital organs. Physicochemical parameters such as pH, electrical conductivity, total dissolved solids, salinity and dissolved oxygen were analyzed. For revealing the ground water quality and soil quality in area of Jammu, a total of 40 samples have been collected and analyzed for different kind of heavy metal concentration. These heavy metal concentrations in water samples were analyzed by Atomic Absorption Spectrophotometer (AAS). The results were compared with WHO, ED, ICMR and Indian. The trace metal analysis is not on the exceeding side of the permissible limit in all the samples. Along with the heavy metal concentration in water samples and soil samples, the radon concentration also measured by using RAD7. The values of radon concentration in drinking water samples were also compared within the safe limit recommended by different health agencies. (author)

  11. Detection of Waterborne Protozoa, Viruses, and Bacteria in Groundwater and Other Water Samples in the Kathmandu Valley, Nepal

    Science.gov (United States)

    Haramoto, E.

    2018-03-01

    In this study, the prevalence of various waterborne pathogens in water samples collected in the Kathmandu Valley, Nepal, and the applicability of Escherichia coli as an indicator of pathogen contamination in groundwater were assessed. Fifty-three water samples, including shallow groundwater and river water, were analyzed to examine the presence of protozoan (oo)cysts via fluorescence microscopy and that of viral and bacterial genomes via quantitative PCR. At least one of the seven types of pathogens tested (i.e., Cryptosporidium, Giardia, human adenoviruses, noroviruses of genogroups I and II, group A rotaviruses, and Vibrio cholerae) was detected in 68% (15/22) of the shallow dug well water samples; groundwater in the shallow dug wells was more contaminated compared with that in shallow tube wells (8/15, 53%). River water and sewage samples were contaminated with extremely high concentrations of multiple pathogens, whereas a tap water sample supplied by a water tanker tested positive for human adenoviruses and V. cholerae. The detection of host-specific Bacteroidales genetic markers revealed the effects of human and animal feces on groundwater contamination. The tested pathogens were sometimes detected even in E. coli-negative groundwater samples, indicative of the limitations of using E. coli as an indicator for waterborne pathogens in groundwater.

  12. Effects of water treatment and sample granularity on radiation sensitivity and stability of EPR signals in X-ray irradiated bone samples

    International Nuclear Information System (INIS)

    Ciesielski, Bartlomiej; Krefft, Karolina; Penkowski, Michal; Kaminska, Joanna; Drogoszewska, Barbara

    2014-01-01

    The article describes effects of sample conditions during its irradiation and electron paramagnetic resonance (EPR) measurements on the background (BG) and dosimetric EPR signals in bone. Intensity of the BG signal increased up to two to three times after crushing of bone to sub-millimetre grains. Immersion of samples in water caused about 50 % drop in intensity of the BG component followed by its regrowth in 1-2 months. Irradiation of bone samples produced an axial dosimetric EPR signal (radiation-induced signal) attributed to hydroxyapatite component of bone. This signal was stable and was not affected by water. In samples irradiated in dry conditions, EPR signal similar to the native BG was also generated by radiation. In samples irradiated in wet conditions, this BG-like component was initially much smaller than in bone irradiated as dry, but increased in time, reaching similar levels as in dry-irradiated samples. It is concluded that accuracy of EPR dosimetry in bones can be improved, if calibration of the samples is done by their irradiations in wet conditions. (authors)

  13. Determination of Physicals, Chemical, Biologicals and Radioactivity Parameters of Sediments and Water Samples of Seropan River of First Period

    International Nuclear Information System (INIS)

    Tri Rusmanto; Agus Taftazani

    2007-01-01

    Seropan river water quality as residential water resources can be controlled by physical, chemical, and biological parameters. The water quality with the parameters of temperature, suspended solid (SS), gross β radioactivity, hardwater, COD, BOD, Escherichia Coli have been experimentally conducted. The sediment and water samples have been taken at February and August 2006. Measurement result of Seropan river water quality showed that the temperature was 28°C, maximum SS was 48 mg/L, maximum pH was 6.8 maximum hardwater was 257.49 mg/L, maximum COD was 8 mg/L, maximum BOD was 4.9 mg/L, maximum bacteria E. coli > 2400 mpn/100 mL, maximum water gross β was 0.9071 Bq/L. All the parameters were lower than maximum permissible for water condition that decided by Governor of Yogyakarta Special Province No/214/Kpts/1991 and Public Health Minister of Republic of Indonesia Number 907/Menkes/SK/VlI/2002. Sediment sample can not be evaluated because it was not included yet in the river water quality natural radionuclides gamma transmitter identified in river water samples were Tl-208 and K-40. More element detected in sediment samples, they were, Tl-208, Ac-228, Ra-226, Pb-212, Pb-214, Bi-214, Ac-228, Ac-228 and of K-40. (author)

  14. A Numerical Investigation on the Effect of Gas Pressure on the Water Saturation of Compacted Bentonite-Sand Samples

    Directory of Open Access Journals (Sweden)

    Jiang-Feng Liu

    2017-01-01

    Full Text Available In deep geological disposal for high-level radioactive waste, the generated gas can potentially affect the sealing ability of bentonite buffers. There is a competition between water and gas: the former provides sealing by swelling bentonite, and the latter attempts to desaturate the bentonite buffer. Thus, this study focused on numerically modelling the coupling effects of water and gas on the water saturation and sealing efficiency of compacted bentonite-sand samples. Different gas pressures were applied to the top surface of an upper sample, whereas the water pressure on the bottom side of the lower sample was maintained at 4 MPa. The results indicated that gas pressure did not significantly affect the saturation of the bentonite-sand sample until 2 MPa. At 2 MPa, the degree of water saturation of the upper sample was close to 1.0. As the gas pressure increased, this influence was more apparent. When the gas pressure was 6 MPa or higher, it was difficult for the upper sample to become fully saturated. Additionally, the lower sample was desaturated due to the high gas pressure. This indicated that gas pressure played an important role in the water saturation process and can affect the sealing efficiency of bentonite-based buffer materials.

  15. Detection of viable Helicobacter pylori inside free-living amoebae in wastewater and drinking water samples from Eastern Spain.

    Science.gov (United States)

    Moreno-Mesonero, Laura; Moreno, Yolanda; Alonso, José Luis; Ferrús, M Antonia

    2017-10-01

    Helicobacter pylori is one of the most concerning emerging waterborne pathogens. It has been suggested that it could survive in water inside free-living amoebae (FLA), but nobody has studied this relationship in the environment yet. Thus, we aimed to detect viable H. pylori cells from inside FLA in water samples. Sixty-nine wastewater and 31 drinking water samples were collected. FLA were purified and identified by PCR and sequencing. For exclusively detecting H. pylori inside FLA, samples were exposed to sodium hypochlorite and assayed by specific PMA-qPCR, DVC-FISH and culture. FLA were detected in 38.7% of drinking water and 79.7% of wastewater samples, even after disinfection. In wastewater, Acanthamoeba spp. and members of the family Vahlkampfiidae were identified. In drinking water, Acanthamoeba spp. and Echinamoeba and/or Vermamoeba were present. In 39 (58.2%) FLA-positive samples, H. pylori was detected by PMA-qPCR. After DVC-FISH, 21 (31.3%) samples harboured viable H. pylori internalized cells. H. pylori was cultured from 10 wastewater samples. To our knowledge, this is the first report that demonstrates that H. pylori can survive inside FLA in drinking water and wastewater, strongly supporting the hypothesis that FLA could play an important role in the transmission of H. pylori to humans. © 2017 Society for Applied Microbiology and John Wiley & Sons Ltd.

  16. National Coral Reef Monitoring Program: Water Chemistry of the Coral Reefs in the Northwestern Hawaiian Islands from Water Samples collected in 2015 (NCEI Accession 0160330)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water samples are collected and analyzed to assess spatial and temporal variation in the seawater carbonate systems of coral reef ecosystems in the Hawaiian and...

  17. National Coral Reef Monitoring Program: Water Chemistry of the Coral Reefs in the Hawaiian Archipelago from Water Samples collected since 2013

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water samples are collected and analyzed to assess spatial and temporal variation in the seawater carbonate systems of coral reef ecosystems in the Hawaiian and...

  18. National Coral Reef Monitoring Program: Water Chemistry of the Coral Reefs in the Mariana Archipelago from Water Samples collected in 2014

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water samples are collected and analyzed to assess spatial and temporal variation in the seawater carbonate systems of coral reef ecosystems in the Hawaiian and...

  19. National Coral Reef Monitoring Program: Water Chemistry of the Coral Reefs in the Pacific Remote Island Areas from Water Samples collected in 2015 (NCEI Accession 0159169)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water samples are collected and analyzed to assess spatial and temporal variation in the seawater carbonate systems of coral reef ecosystems in the Hawaiian and...

  20. National Coral Reef Monitoring Program: Water Chemistry of the Coral Reefs in the Pacific Remote Island Areas from Water Samples collected since 2014

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water samples are collected and analyzed to assess spatial and temporal variation in the seawater carbonate systems of coral reef ecosystems in the Hawaiian and...

  1. Just add water: Accuracy of analysis of diluted human milk samples using mid-infrared spectroscopy.

    Science.gov (United States)

    Smith, R W; Adamkin, D H; Farris, A; Radmacher, P G

    2017-01-01

    To determine the maximum dilution of human milk (HM) that yields reliable results for protein, fat and lactose when analyzed by mid-infrared spectroscopy. De-identified samples of frozen HM were obtained. Milk was thawed and warmed (40°C) prior to analysis. Undiluted (native) HM was analyzed by mid-infrared spectroscopy for macronutrient composition: total protein (P), fat (F), carbohydrate (C); Energy (E) was calculated from the macronutrient results. Subsequent analyses were done with 1 : 2, 1 : 3, 1 : 5 and 1 : 10 dilutions of each sample with distilled water. Additional samples were sent to a certified lab for external validation. Quantitatively, F and P showed statistically significant but clinically non-critical differences in 1 : 2 and 1 : 3 dilutions. Differences at higher dilutions were statistically significant and deviated from native values enough to render those dilutions unreliable. External validation studies also showed statistically significant but clinically unimportant differences at 1 : 2 and 1 : 3 dilutions. The Calais Human Milk Analyzer can be used with HM samples diluted 1 : 2 and 1 : 3 and return results within 5% of values from undiluted HM. At a 1 : 5 or 1 : 10 dilution, however, results vary as much as 10%, especially with P and F. At the 1 : 2 and 1 : 3 dilutions these differences appear to be insignificant in the context of nutritional management. However, the accuracy and reliability of the 1 : 5 and 1 : 10 dilutions are questionable.

  2. Free water {sup 3}H concentration in diet samples collected during 1969-88 in Akita, Japan

    Energy Technology Data Exchange (ETDEWEB)

    Hisamatsu, S. [Institute for Environmental Sciences, Rokkasho, Aomori (Japan); Inoue, Y.; Miyamoto, K. [National Inst. of Radiological Sciences, Chiba (Japan); Takizawa, Y. [National Institute for Minamata Disease, Minamata, Kumamoto (Japan)

    2000-05-01

    Fallout {sup 3}H concentrations in diet samples collected during 1969-88 in Akita Prefecture are reported in this paper. Since {sup 3}H is a potential nuclear fuel for fusion reactors in future, its environmental behavior is important for dose assessment of released {sup 3}H from the plants. Tritium in foods is classified into two types; free water {sup 3}H (FWT) and organically-bound {sup 3}H (OBT). The FWT is practically separated by means of freeze-drying, while the OBT is measured with water sample collected by combustion of dried sample. The OBT concentrations in foods and human tissue samples were reported for {sup 3}H originating from nuclear weapon fallout. We already published {sup 3}H concentrations in diet samples collected in Akita City during 1985-88. Although results for the samples collected in U.S.A. and European countries in the 1970s showed higher specific activity of OBT than FWT, our recent results in Japan indicate almost the same specific activity between them. Since the measurements for the samples in 1960s and 1970s are important to understand the long-term movement of {sup 3}H in the environment, we have searched old diet samples. Recently, diet samples collected in Akita Prefecture during 1969-80 were found and obtained for {sup 3}H analysis. The samples were originally gathered for nutrition survey programs and consisted of duplicate diet samples for 1 day from 10-30 persons. Food samples excluding boiled rice which is the staple food was homogenized by electric mixers after adding tap water. Then, the food and the boiled rice samples were stored in a refrigerator at -20degC. Free water in the samples was collected with lyophilization, then {sup 3}H in the water sample was measured after purification with low-level liquid scintillation counters. The free water {sup 3}H concentrations were measured for 57 diet samples (dish excluding boiled rice) and 17 boiled rice samples. The free water {sup 3}H concentrations in diet and rice samples

  3. Improving the Accuracy of the Hyperspectral Model for Apple Canopy Water Content Prediction using the Equidistant Sampling Method.

    Science.gov (United States)

    Zhao, Huan-San; Zhu, Xi-Cun; Li, Cheng; Wei, Yu; Zhao, Geng-Xing; Jiang, Yuan-Mao

    2017-09-11

    The influence of the equidistant sampling method was explored in a hyperspectral model for the accurate prediction of the water content of apple tree canopy. The relationship between spectral reflectance and water content was explored using the sample partition methods of equidistant sampling and random sampling, and a stepwise regression model of the apple canopy water content was established. The results showed that the random sampling model was Y = 0.4797 - 721787.3883 × Z 3 - 766567.1103 × Z 5 - 771392.9030 × Z 6 ; the equidistant sampling model was Y = 0.4613 - 480610.4213 × Z 2 - 552189.0450 × Z 5 - 1006181.8358 × Z 6 . After verification, the equidistant sampling method was verified to offer a superior prediction ability. The calibration set coefficient of determination of 0.6599 and validation set coefficient of determination of 0.8221 were higher than that of the random sampling model by 9.20% and 10.90%, respectively. The root mean square error (RMSE) of 0.0365 and relative error (RE) of 0.0626 were lower than that of the random sampling model by 17.23% and 17.09%, respectively. Dividing the calibration set and validation set by the equidistant sampling method can improve the prediction accuracy of the hyperspectral model of apple canopy water content.

  4. Metal-organic framework based in-syringe solid-phase extraction for the on-site sampling of polycyclic aromatic hydrocarbons from environmental water samples.

    Science.gov (United States)

    Zhang, Xiaoqiong; Wang, Peiyi; Han, Qiang; Li, Hengzhen; Wang, Tong; Ding, Mingyu

    2018-04-01

    In-syringe solid-phase extraction is a promising sample pretreatment method for the on-site sampling of water samples because of its outstanding advantages of portability, simple operation, short extraction time, and low cost. In this work, a novel in-syringe solid-phase extraction device using metal-organic frameworks as the adsorbent was fabricated for the on-site sampling of polycyclic aromatic hydrocarbons from environmental waters. Trace polycyclic aromatic hydrocarbons were effectively extracted through the self-made device followed by gas chromatography with mass spectrometry analysis. Owing to the excellent adsorption performance of metal-organic frameworks, the analytes could be completely adsorbed during one adsorption cycle, thus effectively shortening the extraction time. Moreover, the adsorbed analytes could remain stable on the device for at least 7 days, revealing the potential of the self-made device for on-site sampling of degradable compounds in remote regions. The limit of detection ranged from 0.20 to 1.9 ng/L under the optimum conditions. Satisfactory recoveries varying from 84.4 to 104.5% and relative standard deviations below 9.7% were obtained in real samples analysis. The results of this study promote the application of metal-organic frameworks in sample preparation and demonstrate the great potential of in-syringe solid-phase extraction for the on-site sampling of trace contaminants in environmental waters. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Data Validation Package April 2016 Groundwater and Surface Water Sampling at the Monticello, Utah, Disposal and Processing Sites August 2016

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, Jason [USDOE Office of Legacy Management, Washington, DC (United States); Smith, Fred [Navarro Research and Engineering, Oak Ridge, TN (United States)

    2016-08-01

    This semiannual event includes sampling groundwater and surface water at the Monticello Disposal and Processing Sites. Sampling and analyses were conducted as specified in the Sampling and Analysis Plan for U.S. Department of Energy Office of Legacy Management Sites (LMS/PRO/S04351, continually updated) and Program Directive MNT-2016-01. Complete sample sets were collected from 42 of 48 planned locations (9 of 9 former mill site wells, 13 of 13 downgradient wells, 7 of 9 downgradient permeable reactive barrier wells, 4 of 7 seeps and wetlands, and 9 of 10 surface water locations). Planned monitoring locations are shown in Attachment 1, Sampling and Analysis Work Order. Locations R6-M3, SW00-01, Seep 1, Seep 2, and Seep 5 were not sampled due to insufficient water availability. A partial sample was collected at location R4-M3 due to insufficient water. All samples from the permeable reactive barrier wells were filtered as specified in the program directive. Duplicate samples were collected from surface water location Sorenson and from monitoring wells 92-07 and RlO-Ml. Water levels were measured at all sampled wells and an additional set of wells. See Attachment2, Trip Report for additional details. The contaminants of concern (COCs) for the Monticello sites are arsenic, manganese, molybdenum, nitrate+ nitrite as nitrogen (nitrate+ nitrite as N), selenium, uranium, and vanadium. Locations with COCs that exceeded remediation goals are listed in Table 1 and Table 2. Time-concentration graphs of the COCs for all groundwater and surface water locations are included in Attachment 3, Data Presentation. An assessment of anomalous data is included in Attachment 4.

  6. 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

  7. Intercomparison of radionuclide measurements in Baltic Sea water sample IAEA-299

    International Nuclear Information System (INIS)

    Ballestra, S.; Lopez, J.J.

    1993-03-01

    This report contains the results of the intercomparison exercise on IAEA-299 for the determination of 90 Sr, 134 Cs and 137 Cs concentration in Baltic Sea Water. The participants belong to 8 laboratories located in 6 countries, members of the Helsinki commission. Statistical evaluation of the data reported yields to recommended values for these elements. The elements, their recommended values and confidence intervals are listed here: 90 Sr: 13.6 Bq kg -1 (12.8-14.4); 134 Cs: 6.7 Bq kg -1 (5-8.3); 137 Cs: 70.9 Bq kg -1 (68-72.3). Reference date: 27 June 1991 (sampling date). The data reported by the laboratories of the Baltic Sea States are generally in very good agreement. (author)

  8. Determination of cadmium in real water samples by flame atomic absorption spectrometry after cloud point extraction

    International Nuclear Information System (INIS)

    Naeemullah, A.; Kazi, T.G.

    2011-01-01

    Water pollution is a global threat and it is the leading world wide cause of death and diseases. The awareness of the potential danger posed by heavy metals to the ecosystems and in particular to human health has grown tremendously in the past decades. Separation and preconcentration procedures are considered of great importance in analytical and environmental chemistry. Cloud point is one of the most reliable and sophisticated separation methods for determination of traces quantities of heavy metals. Cloud point methodology was successfully employed for preconcentration of trace quantities of cadmium prior to their determination by flame atomic absorption spectrometry (FAAS). The metals react with 8-hydroxquinoline in a surfactant Triton X-114 medium. The following parameters such as pH, concentration of the reagent and Triton X-114, equilibrating temperature and centrifuging time were evaluated and optimized to enhance the sensitivity and extraction efficiency of the proposed method. Dilution of the surfactant-rich phase with acidified ethanol was performed after phase separation and the cadmium content was measured by FAAS. The validation of the procedure was carried out by spiking addition methods. The method was applied for determination of Cd in water samples of different ecosystems (lake and river). (author)

  9. Alternative sorptive extraction method for gas chromatography determination of halogenated anisoles in water and wine samples

    International Nuclear Information System (INIS)

    Montes, R.; Rodriguez, I.; Rubi, E.; Bollain, M.H.; Cela, R.

    2007-01-01

    An alternative sorptive microextraction method for the determination of five halogenated anisoles in water and wine matrices is proposed. Analytes were concentrated in an inexpensive and disposable piece of bulk polydimethylsiloxane (PDMS), desorbed with a small volume of organic solvent, and determined by gas chromatography with electron-capture detection (GC-ECD) or tandem mass spectrometry (GC-MS/MS). The influence of several factors on the efficiency of extraction and desorption steps was investigated in detail and the observed behaviour justified on the basis of thermodynamics and kinetics of the solid-phase microextraction technique. Under optimised conditions, analytes were first extracted in the headspace (HS) mode, at room temperature, for 2.5 h and then desorbed with 1 mL of n-pentane. This extract was further evaporated to 50 μL. The overall extraction yield of the procedure ranged from 40 to 55% and the limits of quantification remained between 0.5 and 20 ng L -1 , depending on the compound considered and the detection technique. Precision and linearity of the method were excellent for all species with both GC-ECD and GC-MS/MS detection. Matrix effects were evaluated with different water and wine samples; moreover, the suitability of the PDMS sorbent for storage of analytes, under different conditions, was demonstrated

  10. Alternative sorptive extraction method for gas chromatography determination of halogenated anisoles in water and wine samples

    Energy Technology Data Exchange (ETDEWEB)

    Montes, R. [Departamento de Quimica Analitica, Nutricion y Bromatologia, Instituto de Investigacion y Analisis Alimentario, Universidad de Santiago de Compostela, Santiago de Compostela 15782 (Spain); Rodriguez, I. [Departamento de Quimica Analitica, Nutricion y Bromatologia, Instituto de Investigacion y Analisis Alimentario, Universidad de Santiago de Compostela, Santiago de Compostela 15782 (Spain)], E-mail: qnisaac@usc.es; Rubi, E.; Bollain, M.H.; Cela, R. [Departamento de Quimica Analitica, Nutricion y Bromatologia, Instituto de Investigacion y Analisis Alimentario, Universidad de Santiago de Compostela, Santiago de Compostela 15782 (Spain)

    2007-09-05

    An alternative sorptive microextraction method for the determination of five halogenated anisoles in water and wine matrices is proposed. Analytes were concentrated in an inexpensive and disposable piece of bulk polydimethylsiloxane (PDMS), desorbed with a small volume of organic solvent, and determined by gas chromatography with electron-capture detection (GC-ECD) or tandem mass spectrometry (GC-MS/MS). The influence of several factors on the efficiency of extraction and desorption steps was investigated in detail and the observed behaviour justified on the basis of thermodynamics and kinetics of the solid-phase microextraction technique. Under optimised conditions, analytes were first extracted in the headspace (HS) mode, at room temperature, for 2.5 h and then desorbed with 1 mL of n-pentane. This extract was further evaporated to 50 {mu}L. The overall extraction yield of the procedure ranged from 40 to 55% and the limits of quantification remained between 0.5 and 20 ng L{sup -1}, depending on the compound considered and the detection technique. Precision and linearity of the method were excellent for all species with both GC-ECD and GC-MS/MS detection. Matrix effects were evaluated with different water and wine samples; moreover, the suitability of the PDMS sorbent for storage of analytes, under different conditions, was demonstrated.

  11. Method validation using weighted linear regression models for quantification of UV filters in water samples.

    Science.gov (United States)

    da Silva, Claudia Pereira; Emídio, Elissandro Soares; de Marchi, Mary Rosa Rodrigues

    2015-01-01

    This paper describes the validation of a method consisting of solid-phase extraction followed by gas chromatography-tandem mass spectrometry for the analysis of the ultraviolet (UV) filters benzophenone-3, ethylhexyl salicylate, ethylhexyl methoxycinnamate and octocrylene. The method validation criteria included evaluation of selectivity, analytical curve, trueness, precision, limits of detection and limits of quantification. The non-weighted linear regression model has traditionally been used for calibration, but it is not necessarily the optimal model in all cases. Because the assumption of homoscedasticity was not met for the analytical data in this work, a weighted least squares linear regression was used for the calibration method. The evaluated analytical parameters were satisfactory for the analytes and showed recoveries at four fortification levels between 62% and 107%, with relative standard deviations less than 14%. The detection limits ranged from 7.6 to 24.1 ng L(-1). The proposed method was used to determine the amount of UV filters in water samples from water treatment plants in Araraquara and Jau in São Paulo, Brazil. Copyright © 2014 Elsevier B.V. All rights reserved.

  12. Identification of pink-pigmented bacteria isolated from environmental water samples and their biofilm formation abilities.

    Science.gov (United States)

    Furuhata, Katsunori; Kato, Yuko; Goto, Keiichi; Saitou, Keiko; Sugiyama, Jun-Ichi; Hara, Motonobu; Fukuyama, Masahumi

    2008-06-01

    Sixty-seven strains of pink-pigmented bacteria, which were isolated from environmental water samples collected nationwide, were identified by partial 16S rDNA sequence analysis. In addition, the biofilm formation ability of the isolates was experimentally investigated. We could identify only 2 strains at the species level: Pedobacter roseus HS-38 and Runella slithyformis HS-77. The results showed that of the strains tested, 22 strains (32.8%) were Pedobacter spp., which was most frequently identified, followed by 19 strains (28.4%) of Arcicella spp., 16 strains (23.9%) of Deinococcus spp., 5 strains (7.5%) of Roseomonas spp., 4 strains (6.0%) of Flectobacillus spp. and 1 strain (1.5%) of Runella sp. Most isolates showed low similarity values to previously known species, and they were found to be novel species. At a result, it was difficult to identify environmental water-derived pink-pigmented bacteria at the species level. On the other hand, when we measured the absorbance by the