WorldWideScience

Sample records for chemistry water

  1. Water Chemistry: Seeking Information

    Science.gov (United States)

    Delfino, Joseph J.

    1977-01-01

    A survey of the available literature in water chemistry is presented. Materials surveyed include: texts, reference books, bibliographic resources, journals, American Chemical Society publications, proceedings, unpublished articles, and reports. (BT)

  2. Water Chemistry Laboratory Manual.

    Science.gov (United States)

    Jenkins, David; And Others

    This manual of laboratory experiments in water chemistry serves a dual function of illustrating fundamental chemical principles of dilute aqueous systems and of providing the student with some familiarity with the chemical measurements commonly used in water and wastewater analysis. Experiments are grouped in categories on the basis of similar…

  3. Supramolecular Chemistry in Water

    NARCIS (Netherlands)

    Oshovsky, Gennady V.; Reinhoudt, David N.; Verboom, Willem

    2007-01-01

    Supramolecular chemistry in water is a constantly growing research area because noncovalent interactions in aqueous media are important for obtaining a better understanding and control of the major processes in nature. This Review offers an overview of recent advances in the area of water-soluble sy

  4. Green chemistry oriented organic synthesis in water.

    Science.gov (United States)

    Simon, Marc-Olivier; Li, Chao-Jun

    2012-02-21

    The use of water as solvent features many benefits such as improving reactivities and selectivities, simplifying the workup procedures, enabling the recycling of the catalyst and allowing mild reaction conditions and protecting-group free synthesis in addition to being benign itself. In addition, exploring organic chemistry in water can lead to uncommon reactivities and selectivities complementing the organic chemists' synthetic toolbox in organic solvents. Studying chemistry in water also allows insight to be gained into Nature's way of chemical synthesis. However, using water as solvent is not always green. This tutorial review briefly discusses organic synthesis in water with a Green Chemistry perspective.

  5. Updating the EPRI guidelines (water chemistry)

    Energy Technology Data Exchange (ETDEWEB)

    Jones, R.L.; Welty, C.S.; Wood, C.J.

    1988-03-01

    Significant improvements in water chemistry have been achieved in recent years at US nuclear plants, at least in part as a result of implementing water chemistry guidelines. These guidelines were prepared by industry committees, comprised of utilities and NSSS vendors and chaired by EPRI.

  6. Fog water chemistry in Shanghai

    Science.gov (United States)

    Li, Pengfei; Li, Xiang; Yang, Chenyu; Wang, Xinjun; Chen, Jianmin; Collett, Jeffrey L., Jr.

    2011-08-01

    With the aim of understanding the fog chemistry in a Chinese megacity, twenty-six fog water samples were collected in urban Shanghai from March 2009 to March 2010. The following parameters were measured: pH, electrical conductivity (EC), ten inorganic major ions ( SO42-, NO3-, NO2-, F -, Cl -, Na +, K +, Ca 2+, Mg 2+, NH4+) and four major organic acids (CH 3COO -, HCOO -, CO42-, MSA). The total ionic concentration (TIC) and EC of fog samples were one or two orders of magnitude higher than those often found in Europe, North America and other Asian countries. Pollutants were expected to be mainly from local sources, including factories, motor vehicle emissions and civil construction. Non-local sources such as moderate- and long-range transport of sea salt also contributed to pollution levels in fog events as indicated by back trajectory analysis. The pH of the fog water collected during the monitoring period varied from 4.68 to 6.58; acidic fogs represented about 30.8% of the total fog events during this period. The fog water was characterized by high concentrations of SO42- (20.0% of measured TIC), NO3- (17.1%), NH4+ (28.3%) and Ca 2+ (14.4%). SO42- and NO3-, the main precursors of fog acidity, were related to burning fossil fuels and vehicle emissions, respectively. NH4+, originating from the scavenging of gaseous ammonia and particulate ammonium nitrate and ammonium sulfate, and Ca 2+, originating from the scavenging of coarse particles, acted as acid neutralizers and were the main cause for the relatively high pH of fogs in Shanghai. The ratio of ( SO42- + NO3-)/( NH4+ + Ca 2+) was lower than 1, indicating the alkaline nature of the fog water. A high ratio of NO3-/ SO42- and low ratio of HCOO -/CH 3COO - were consistent with large contributions from vehicular emissions that produce severe air pollution in megacities.

  7. Interstellar water chemistry: from laboratory to observations

    CERN Document Server

    van Dishoeck, Ewine F; Neufeld, David A

    2013-01-01

    Water is observed throughout the universe, from diffuse interstellar clouds to protoplanetary disks around young stars, and from comets in our own solar system and exoplanetary atmospheres to galaxies at high redshifts. This review summarizes the spectroscopy and excitation of water in interstellar space as well as the basic chemical processes that form and destroy water under interstellar conditions. Three major routes to water formation are identified: low temperature ion-molecule chemistry, high-temperature neutral-neutral chemistry and gas-ice chemistry. The rate coefficients of several important processes entering the networks are discussed in detail; several of them have been determined only in the last decade through laboratory experiments and theoretical calculations. Astronomical examples of each of the different chemical routes are presented using data from powerful new telescopes, in particular the Herschel Space Observatory. Basic chemical physics studies remain critically important to analyze ast...

  8. Inorganic chemistry: Deconstructing water oxidation

    Science.gov (United States)

    Cook, Sarah A.; Borovik, A. S.

    2013-04-01

    During photosynthesis, the oxygen-evolving complex oxidizes water to produce molecular oxygen. Now, a possible role for the calcium ion in this complex has been proposed based on the electrochemical properties of a series of synthetic heterometallic clusters.

  9. Montane wetland water chemistry, Uinta Mountains, Utah

    Science.gov (United States)

    Severson, K. S.; Matyjasik, M.; Ford, R. L.; Hernandez, M. W.; Welsh, S. B.; Summers, S.; Bartholomew, L. M.

    2009-12-01

    This study attempts to determine the relationship between surface and groundwater chemistry and wetland characteristics within the Reader Lakes watershed, Uinta Mountains. The dominant rock type in the study area is quartz sandstone of the Hades Pass formation, Unita Mountain Group (Middle Proterozoic). Minor amounts of interbedded arkose and illite-bearing shale are also present. Water chemistry data have been collected from more than one hundred locations during the 2008 and 2009 summer seasons. The Reader Creek watershed is approximately 9.8 km long and about 3.5 km wide in the central portion of the basin. Direct precipitation is the primary source of groundwater recharge and the area is typically covered by snow from November until May. Four distinct wetland complexes, designated as the upper, middle, lower and the sloping fen, constitute the major wetland environments in the study area. The chemistry of the melt water from the high-elevation snowfield is affected by weathering of incorporated atmospheric dust and surface rocks. Total dissolved solids in both years were between 7 and 9 mg/L. Major anions include HCO3 (averaging 4.0 mg/L), SO4 (1.3 mg/L), NO3 (0.9 mg/L), Cl (0.8 mg/L), F (0.07 mg/L), PO4 (0.03 mg/L), and Br(0.015 mg/L). Major cations include Na (1.1 mg/L), Ca (1.0 mg/L), K (0.28 mg/L), and Mg (0.15 mg/L). Groundwater concentrations in the lower meadow, as measured in piezomters, are distinctly different, with the following maximum concentrations of anions: HCO3 (36.7 mg/L), SO4 (5.0 mg/L), Cl (3.4 mg/L), NO3 (0.9 mg/L), PO4 (0.28 mg/L), F (0.23 mg/L), Br (0.12 mg/L), and cations: Ca (22 mg/L), Na (4.6 mg/L), Mg (3.4 mg/L), and K (1.8 mg/L)- with a maximum value of 83 mg/L for total dissolved solids. Waters in Reader Creek, the main trunk channel, are typically sodium-potassium and sodium -potassium bicarbonate, with some calcium-bicarbonate, mostly in the middle part of the watershed. Groundwater from springs is sodium-potassium in the upper

  10. Water chemistry model development at Total EandP Canada: modeling uncertainty in ore chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Kaminsky, H.A.W.; Yoo, A.; Schaffer, M. [Total EandP Canada Ltd. (Canada)

    2011-07-01

    In oil sands mining operations, water chemistry is a key factor as it plays a role in the bitumen recovery and water discharge to the environment. Total Canada have developed a new water chemistry model combining the previous models developed by Rogers and Kasperski and making modifications to improve reliability of the results. Two challenges had to be addressed in the development of this model: making sure that the data used were appropriate, and accurately modeling uncertainty. The aim of this paper is to present the modifications made to the model and other water chemistry models. Laboratory tests were conducted using the double leach and the standard leach methods. Results showed that the standard leach method provides more accurate measurement on batch extraction tests. This paper outlined the challenges of developing a new prediction model; further tests are needed to determine the best method to use in describing ore chemistry.

  11. Water chemistry at RBMK plants: Problems and solutions

    Energy Technology Data Exchange (ETDEWEB)

    Mamet, V.; Yurmanov, V. [VNIIAES (Russian Federation)

    2002-07-01

    After around 15 years of operation RBMK-1000 units undergo a major refit, which includes safety system upgrading, fuel tube replacement, etc. The above upgrading has created problems for water chemistry. In particular, in late 80's in-core insertion time of the portion of control rods was reduced 10-fold thanks to a transfer from water to filming cooling of scram channels. Scram channels are cooled with inner surface water film cooling and nitrogen is injected into heads via special pipelines. Such cooling system modernization ensures fast insertion of absorber rods. The above upgrade intensified nitric acid radiolytic generation in water coolant and pH{sub 25} value shift to acid conditions (up to 4.5). The results of corrosion tests in such conditions proved the necessity to improve water chemistry to ensure corrosion protection of scram/control rod and circuit components, especially those made out of aluminium alloy. Since 1990 the new revision of the RBMK-1000 water chemistry standard specified the new normal operational limit and action levels for possible temporary deviations of pH{sub 25} value. RBMK plant specific measures were implemented at RBMK plants to meet the above requirements of the 1990 revision of the RBMK-1000 water chemistry standard. Clean-up systems of the above circuit were upgraded to ensure intensive absorption of nitric acid from water and pH{sub 25} maintenance in a slightly acid area. (authors)

  12. Water chemistry: fifty years of change and progress.

    Science.gov (United States)

    Brezonik, Patrick L; Arnold, William A

    2012-06-05

    Water chemistry evolved from early foundations in several related disciplines. Although it is difficult to associate a precise date to its founding, several events support the argument that the field as we know it today developed in the mid-20th century--at the dawn of the "environmental era"--that is, ∼1960. The field in its modern incarnation thus is about 50 years old. In celebration of this half-centenary, we examine here the origins of water chemistry, how the field has changed over the past 50 years, and the principal driving forces for change, focusing on both the "practice" of water chemistry and ways that teaching the subject has evolved.

  13. Par Pond Fish, Water, and Sediment Chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Paller, M.H. [Westinghouse Savannah River Company, AIKEN, SC (United States); Wike, L.D.

    1996-06-01

    The objectives of this report are to describe the Par Pond fish community and the impact of the drawdown and refill on the community, describe contaminant levels in Par Pond fish, sediments, and water and indicate how contaminant concentrations and distributions were affected by the drawdown and refill, and predict possible effects of future water level fluctuations in Par Pond.

  14. Environmental Chemistry: Air and Water Pollution.

    Science.gov (United States)

    Stoker, H. Stephen; Seager, Spencer L.

    This is a book about air and water pollution whose chapters cover the topics of air pollution--general considerations, carbon monoxide, oxides of nitrogen, hydrocarbons and photochemical oxidants, sulfur oxides, particulates, temperature inversions and the greenhouse effect; and water pollution--general considerations, mercury, lead, detergents,…

  15. Water chemistry of Lake Albano (Italy)

    Science.gov (United States)

    Cioni, Roberto; Guidi, Massimo; Raco, Brunella; Marini, Luigi; Gambardella, Barbara

    2003-02-01

    Lake Albano was stratified at the time of our survey, in December 1997, in agreement with previous observations [Martini et al., Geochem. J. 28 (1994) 173-184; Cioni et al., Report for the Civil Protection Department (1995); Pedreschi, Accad. Lucch. Sci. Lett. Arti (1995) 39]. In the absence of phenomena induced by seismic activity, either local or regional, lake stratification may be perturbed by cooling of shallow waters below ˜8.5°C. Circulation is expected to homogenize lake waters and eventually to trigger gas exsolution when total gas pressure exceeds hydrostatic pressure. In December 1997, total gas pressure in lake water was very close to atmospheric pressure (0.9-1.3 bar) at all depths, possibly due to the occurrence of a recent episode of circulation and presumed gas exsolution. The state of saturation of Lake Albano waters and the similarity of the relative concentrations of Na, K, Mg, and Ca in lake waters, local groundwaters, and local volcanic rocks indicate that Na, K, Mg, and Ca concentrations in Lake Albano waters are mainly governed by incongruent dissolution of local volcanic rocks, coupled with minor calcite precipitation at shallow depths.

  16. Apparatus for ground water chemistry investigations in field caissons

    Energy Technology Data Exchange (ETDEWEB)

    Cokal, E.J.; Stallings, E.; Walker, R.; Nyhan, J.W.; Polzer, W.L.; Essington, E.H.

    1985-01-01

    Los Alamos is currently in its second season of ground water chemistry and hydrology experimentation in a field facility that incorporates clusters of six, 3-meter-diameter by 6-meter-deep, soil-filled caissons and required ancillaries. Initial experience gained during the 1983 field season indicated the need for further development of the technology of this type of experimentation supporting hydrologic waste management research. Uniform field application of water/matrix solutions to the caisson, matrix and tracer solution blending/storage, and devices for ground water sampling are discussed.

  17. Radiation Chemistry in Ammonia-Water Ices

    Science.gov (United States)

    Loeffler, M. J.; Raut, U.; Baragiola, R. A.

    2010-01-01

    We studied the effects of 100 keV proton irradiation on films of ammonia-water mixtures between 20 and 120 K. Irradiation destroys ammonia, leading to the formation and trapping of H2, N2 NO, and N2O, the formation of cavities containing radiolytic gases, and ejection of molecules by sputtering. Using infrared spectroscopy, we show that at all temperatures the destruction of ammonia is substantial, but at higher temperatures (120 K), it is nearly complete (approximately 97% destroyed) after a fluence of 10(exp 16) ions per square centimeter. Using mass spectroscopy and microbalance gravimetry, we measure the sputtering yield of our sample and the main components of the sputtered flux. We find that the sputtering yield depends on fluence. At low temperatures, the yield is very low initially and increases quadratically with fluence, while at 120 K the yield is constant and higher initially. The increase in the sputtering yield with fluence is explained by the formation and trapping of the ammonia decay products, N2 and H2 which are seen to be ejected from the ice at all temperatures.

  18. Reacting chemistry at the air-water interface

    Science.gov (United States)

    Murakami, Tomoyuki; Morgan, Thomas; Huwel, Lutz; Graham, William

    2016-09-01

    Plasma interaction with gas-liquid interfaces is becoming increasingly important in biological applications, chemical analysis and medicine. It introduces electrons, new ionic species and reactive species and contributes to chemical and electrical self-organization at the interface. To provide insight into the associated physics and chemistry at work in the evolution of the plasma in the air-water interface (AWI), a time-dependent one-dimensional modelling has been developed. The numerical simulation is used to solve the kinetic equations and help identify the important reaction mechanisms and describe the phenomena associated with hundreds of reacting pathways in gas-phase and liquid-phase AWI chemistry. This work was partly supported by JSPS KAKENHI Grant Number 16K04998.

  19. Water chemistry management of research reactor in JAERI

    Energy Technology Data Exchange (ETDEWEB)

    Yoshijima, Tetsuo [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    1998-10-01

    The JRR-3M cooling system consists of four systems, namely; (1) primary cooling system, (2) heavy water cooling system, (3) helium system and (4) secondary cooling system. The heavy water is used for reflector and pressurized with helium gas. Water chemistry management of the JRR-3M cooling systems is one of the important subject for the safety operation. The main objects are to prevent the corrosion of cooling system and fuel elements, to suppress the plant radiation build-up and to minimize the generation of radioactive waste. All measured values were within the limits of specifications and JRR-3M reactor was operated with safety in 1996. Spent fuels of JRR-3M reactor are stored in the spent fuel pool. This pool water has been analyzed to prevent corrosion of aluminum cladding of spent fuels. Water chemistry of spent fuel pool water is applied to the prevention of corrosion of aluminum alloys including fuel cladding. The JRR-2 reactor was eternally stopped in December 1996 and is now under decommissioning. The JRR-2 reactor is composed of heavy water tank, fuel guide tube and horizontal experimental hole. These are constructed of aluminum alloy and biological shield and upper shield are constructed of concrete. Three types of corrosion of aluminum alloy were observed in the JRR-2. The Alkaline corrosion of aluminum tube occurred in 1972 because of the mechanical damage of the aluminum fuel guide tube which is used for fuel handling. Modification of the reactor top shield was started in 1974 and completed in 1975. (author)

  20. Acid-base chemistry of frustrated water at protein interfaces.

    Science.gov (United States)

    Fernández, Ariel

    2016-01-01

    Water molecules at a protein interface are often frustrated in hydrogen-bonding opportunities due to subnanoscale confinement. As shown, this condition makes them behave as a general base that may titrate side-chain ammonium and guanidinium cations. Frustration-based chemistry is captured by a quantum mechanical treatment of proton transference and shown to remove same-charge uncompensated anticontacts at the interface found in the crystallographic record and in other spectroscopic information on the aqueous interface. Such observations are untenable within classical arguments, as hydronium is a stronger acid than ammonium or guanidinium. Frustration enables a directed Grotthuss mechanism for proton transference stabilizing same-charge anticontacts.

  1. Simulation of Water Chemistry using and Geochemistry Code, PHREEQE

    Energy Technology Data Exchange (ETDEWEB)

    Chi, J.H. [Korea Electric Power Research Institute, Taejeon (Korea)

    2001-07-01

    This report introduces principles and procedures of simulation for water chemistry using a geochemistry code, PHREEQE. As and example of the application of this code, we described the simulation procedure for titration of an aquatic sample with strong acid to investigate the state of Carbonates in aquatic solution. Major contents of this report are as follows; Concepts and principles of PHREEQE, Kinds of chemical reactions which may be properly simulated by PHREEQE, The definition and meaning of each input data, An example of simulation using PHREEQE. (author). 2 figs., 1 tab.

  2. Ferruginous conditions dominated later neoproterozoic deep-water chemistry.

    Science.gov (United States)

    Canfield, Donald E; Poulton, Simon W; Knoll, Andrew H; Narbonne, Guy M; Ross, Gerry; Goldberg, Tatiana; Strauss, Harald

    2008-08-15

    Earth's surface chemical environment has evolved from an early anoxic condition to the oxic state we have today. Transitional between an earlier Proterozoic world with widespread deep-water anoxia and a Phanerozoic world with large oxygen-utilizing animals, the Neoproterozoic Era [1000 to 542 million years ago (Ma)] plays a key role in this history. The details of Neoproterozoic Earth surface oxygenation, however, remain unclear. We report that through much of the later Neoproterozoic (<742 +/- 6 Ma), anoxia remained widespread beneath the mixed layer of the oceans; deeper water masses were sometimes sulfidic but were mainly Fe2+-enriched. These ferruginous conditions marked a return to ocean chemistry not seen for more than one billion years of Earth history.

  3. Comparison of French and German NPP water chemistry programs

    Energy Technology Data Exchange (ETDEWEB)

    Staudt, U. [VGB Powertech (Germany); Odar, S. [Framatome ANP GmbH (Germany); Stutzmann, A. [EDF/GDL (France)

    2002-07-01

    PWRs in the western hemisphere obey basically the same rules concerning design, choice of material and operational mode. In spite of these basic similarities, the manufacturers of PWRs in different countries developed different solutions in respect to single components in the steam/water cycle. Looking specifically at France and Germany, the difference in the tubing material of the steam generators (Inconel 600/690 chosen by Framatome and Incoloy 800 chosen by the former Siemens KWU) led to specific differences in the respective chemistry programs and in some respect to different 'philosophies' in operating the water/steam cycle. Compared to this, basic differences in operating the reactor coolant system cannot be observed. Nevertheless specific solutions as zinc injection and the use of enriched B-10 are applied in German PWRs. The application of such measures arises from a specific dose rate situation in older PWRs (zinc injection) or from economic reasons mainly (B-10). (authors)

  4. Once-through steam generator (OTSG) materials and water chemistry. [PWR

    Energy Technology Data Exchange (ETDEWEB)

    Pocock, F.J.; Levstek, D.F.

    1974-01-01

    Materials and water chemistry research results associated with the development of the Oconee-1 Reactor steam generator are presented. A summary of water chemistry data acquired during preoperational testing and power operation to date is also included. These data confirm the operational practicality of the nuclear once-through concept using volatile water treatment and high purity condensate demineralized feedwater.

  5. Introduction to Chemistry for Water and Wastewater Treatment Plant Operators. Water and Wastewater Training Program.

    Science.gov (United States)

    South Dakota Dept. of Environmental Protection, Pierre.

    Presented are basic concepts of chemistry necessary for operators who manage drinking water treatment plants and wastewater facilities. It includes discussions of chemical terms and concepts, laboratory procedures for basic analyses of interest to operators, and discussions of appropriate chemical calculations. Exercises are included and answer…

  6. Impact of reactor water chemistry on cladding performance

    Energy Technology Data Exchange (ETDEWEB)

    Cox, B. [University of Toronto, Centre for Nuclear Engineering, Toronto, Ontario (Canada)

    1997-07-01

    Water chemistry may have a major impact on fuel cladding performance in PWRs. If the saturation temperature on the surface of fuel cladding is exceeded, either because of the thermal hydraulics of the system, or because of crud deposition, then LiOH concentration can occur within thick porous oxide films on the cladding. This can degrade the protective film and accelerate the corrosion rate of the cladding. If sufficient boric acid is also present in the coolant then these effects may be mitigated. This is normally the case through most of any reactor fuel cycle. Extensive surface boiling may disrupt this equilibrium because of the volatility of boric acid in steam. Under such conditions severe cladding corrosion can ensue. The potential for such effects on high burnup cladding in CANDU reactors, where bone acid is not present in the primary coolant, is discussed. (author)

  7. Pore water chemistry in the beach sands of central Tamil Nadu, India

    Digital Repository Service at National Institute of Oceanography (India)

    Chandrasekar, N.; Gujar, A.R.; Loveson, V.J.; Rajamanickam, G.V.; Moscow, S.; Manickaraj, D; Chandrasekaran, R.; Chaturvedi, S.K.; Mahesh, R.; Sudha, V.; Josephine, P; Deepa, V.

    As the pore water chemistry- has been considered as one of the prominent base parameters to infer the impact of coastal mining in introducing environmental deterioration, a study in pore water chemistry is planned here along the beaches for a length...

  8. Photosynthetic water oxidation: insights from manganese model chemistry.

    Science.gov (United States)

    Young, Karin J; Brennan, Bradley J; Tagore, Ranitendranath; Brudvig, Gary W

    2015-03-17

    Catalysts for light-driven water oxidation are a critical component for development of solar fuels technology. The multielectron redox chemistry required for this process has been successfully deployed on a global scale in natural photosynthesis by green plants and cyanobacteria using photosystem II (PSII). PSII employs a conserved, cuboidal Mn4CaOX cluster called the O2-evolving complex (OEC) that offers inspiration for artificial O2-evolution catalysts. In this Account, we describe our work on manganese model chemistry relevant to PSII, particularly the functional model [Mn(III/IV)2(terpy)2(μ-O)2(OH2)2](NO3)3 complex (terpy = 2,2';6',2″-terpyridine), a mixed-valent di-μ-oxo Mn dimer with two terminal aqua ligands. In the presence of oxo-donor oxidants such as HSO5(-), this complex evolves O2 by two pathways, one of which incorporates solvent water in an O-O bond-forming reaction. Deactivation pathways of this catalyst include comproportionation to form an inactive Mn(IV)Mn(IV) dimer and also degradation to MnO2, a consequence of ligand loss when the oxidation state of the complex is reduced to labile Mn(II) upon release of O2. The catalyst's versatility has been shown by its continued catalytic activity after direct binding to the semiconductor titanium dioxide. In addition, after binding to the surface of TiO2 via a chromophoric linker, the catalyst can be oxidized by a photoinduced electron-transfer mechanism, mimicking the natural PSII process. Model oxomanganese complexes have also aided in interpreting biophysical and computational studies on PSII. In particular, the μ-oxo exchange rates of the Mn-terpy dimer have been instrumental in establishing that the time scale for μ-oxo exchange of high-valent oxomanganese complexes with terminal water ligands is slower than O2 evolution in the natural photosynthetic system. Furthermore, computational studies on the Mn-terpy dimer and the OEC point to similar Mn(IV)-oxyl intermediates in the O-O bond

  9. Multiscale Modeling of Chemistry in Water: Are We There Yet?

    Science.gov (United States)

    Bulo, Rosa E; Michel, Carine; Fleurat-Lessard, Paul; Sautet, Philippe

    2013-12-10

    This paper critically evaluates the state of the art in combined quantum mechanical/molecular mechanical (QM/MM) approaches to the computational description of chemistry in water and supplies guidelines for the setup of customized multiscale simulations of aqueous processes. We differentiate between structural and dynamic performance, since some tasks, e.g., the reproduction of NMR or UV-vis spectra, require only structural accuracy, while others, i.e., reaction mechanisms, require accurate dynamic data as well. As a model system for aqueous solutions in general, the approaches were tested on a QM water cluster in an environment of MM water molecules. The key difficulty is the description of the possible diffusion of QM molecules into the MM region and vice versa. The flexible inner region ensemble separator (FIRES) approach constrains QM solvent molecules within an active (QM) region. Sorted adaptive partitioning (SAP), difference-based adaptive solvation (DAS), and buffered-force (BF) are all adaptive approaches that use a buffer zone in which solvent molecules gradually adapt from QM to MM (or vice versa). The costs of SAP and DAS are relatively high, while BF is fast but sacrifices conservation of both energy and momentum. Simulations in the limit of an infinitely small buffer zone, where DAS and SAP become equivalent, are discussed as well and referred to as ABRUPT. The best structural accuracy is obtained with DAS, BF, and ABRUPT, all three of similar quality. FIRES performs very well for dynamic properties localized deep within the QM region. By means of elimination DAS emerges as the best overall compromise between structural and dynamic performance. Eliminating the buffer zone (ABRUPT) improves efficiency and still leads to surprisingly good results. While none of the many new flavors are perfect, all together this new field already allows accurate description of a wide range of structural and dynamic properties of aqueous solutions.

  10. Handbook of green chemistry, green solvents, reactions in water

    CERN Document Server

    Anastas, Paul T

    2014-01-01

    There has been dramatic growth in the community of researchers and industrialists working in the area of Green Chemistry. There has been an increasing recognition by a wide-range of scientists and engineers in the chemical enterprise that the framework of Green Chemistry is relevant and enabling to their work. There has been a significant body of work that has accumulated over the past decade that details the breakthroughs, innovation and creativity within Green Chemistry and Engineering. While there have been edited volumes on Green Chemistry that collect a limited number of papers often o

  11. Delineating ground water recharge from leaking irrigation canals using water chemistry and isotopes.

    Science.gov (United States)

    Harvey, F E; Sibray, S S

    2001-01-01

    Across the Great Plains irrigation canals are used to transport water to cropland. Many of these canals are unlined, and leakage from them has been the focus of an ongoing legal, economic, and philosophical debate as to whether this lost water should be considered waste or be viewed as a beneficial and reasonable use since it contributes to regional ground water recharge. While historically there has been much speculation about the impact of canal leakage on local ground water, actual data are scarce. This study was launched to investigate the impact of leakage from the Interstate Canal, in the western panhandle of Nebraska, on the hydrology and water quality of the local aquifer using water chemistry and environmental isotopes. Numerous monitoring wells were installed in and around a small wetland area adjacent to the canal, and ground water levels were monitored from June 1992 until January 1995. Using the water level data, the seepage loss from the canal was estimated. In addition, the canal, the monitoring wells, and several nearby stock and irrigation wells were sampled for inorganic and environmental isotope analysis to assess water quality changes, and to determine the extent of recharge resulting from canal leakage. The results of water level monitoring within study wells indicates a rise in local ground water levels occurs seasonally as a result of leakage during periods when the canal is filled. This rise redirects local ground water flow and provides water to nearby wetland ecosystems during the summer months. Chemical and isotopic results were used to delineate canal, surface, and ground water and indicate that leaking canal water recharges both the surface alluvial aquifer and upper portions of the underlying Brule Aquifer. The results of this study indicate that lining the Interstate Canal could lower ground water levels adjacent to the canal, and could adversely impact the local aquifer.

  12. Produced water chemistry data for samples from four petroleum wells, Southern San Joaquin Valley, California, 2014

    Science.gov (United States)

    Davis, Tracy A.; Kulongoski, Justin; McMahon, Peter B.

    2016-01-01

    The U.S. Geological Survey (USGS) in cooperation with the California State Water Resources Control Board collected produced water samples from four petroleum wells in the southern San Joaquin Valley on November 5, 2014. This digital dataset contains the site information, analyzing laboratories and methods, and water chemistry and quality control results for these samples. Water chemistry results include concentrations of dissolved hydrocarbon gases and their isotopic composition; concentrations of inorganic constituents including salinity, major ions, and nutrients; dissolved organic carbon; and stable isotopes of water and strontium dissolved in water. Samples were analyzed by 5 laboratories operated or contracted by the USGS.

  13. Malheur NWR: Initial Survey Instructions for Water Chemistry/Quality Collection of Water Bodies in Malheur National Wildlife Refuge

    Data.gov (United States)

    US Fish and Wildlife Service, Department of the Interior — This survey provides the baseline understanding of aquatic health in our rivers, lakes, and marshes. The Refuge staff lacks consistent water chemistry measurements,...

  14. Evolution of the water chemistry of Lake Orta after liming

    Directory of Open Access Journals (Sweden)

    Gabriele A. TARTARI

    2001-02-01

    Full Text Available Since 1963 Lake Orta has been an emblematic case of industrial pollution by heavy metals and acidifying compounds (ammonium sulphate, to the extent that up to 1989 it was the largest acidified deep lake in the world. The low pH values of between 3.9 and 4.4 helped to keep high the levels of toxic compounds in solution, such as copper, aluminium, zinc and nickel. The liming performed in 1989-1990 brought the pH back to neutral values, determining the precipitation of the metals and the recovery of normal chemical conditions. The main results of researches conducted continuously on the lake water chemistry from 1988 to March 2000 are as follows. The whole water mass has been completely neutralised since the beginning of 1991; pH subsequently rose until in 1999-2000 it reached the values (6.7-6.9 units of the years when the lake was in a natural condition. The alkaline reserve showed a continuous increase after the lake water was neutralised, until March 2000, when total alkalinity values levelled off at 0.19 meq l-1. The increase in pH has allowed a full recovery of nitrification processes; in fact, during the liming period the concentration of ammonium was drastically reduced, by over 80%; ammonium has been practically absent since the end of 1992, and it may be affirmed that the primary cause of the acidification of the lake has been completely removed. The nitrate content in the lake has almost halved compared with the mean concentrations measured before the liming; in March 2000 mean values of 2.0 mg N l-1 were measured, and it is likely that these values will fall further in the next few years, to below 1.5 mg N l-1. The concentrations of toxic metals have shown a progressive reduction, to the extent that in 1999 the content of copper and aluminium was close to zero in the whole water mass. The situation of Lake Orta has therefore improved enormously, and is now very similar to the original condition of the lake before it was polluted

  15. Major ion chemistry of the Son River, India: Weathering processes, dissolved fluxes and water quality assessment

    Indian Academy of Sciences (India)

    Chinmaya Maharana; Sandeep Kumar Gautam; Abhay Kumar Singh; Jayanth K Tripathi

    2015-08-01

    River Son, draining diverse lithologies in the subtropical climate of the peninsular sub-basin of the Ganga basin, is one of the major tributaries of the Ganga River. The chemistry of major ions in the surface water of the Son River was studied in detail to determine various source(s) and processes controlling its water chemistry, seasonal and spatial variations in water chemistry, dissolved fluxes and chemical denudation rate (CDR). The study shows that Ca2+, Mg2+ and HCO$^{-}_{3}$ are major ionic species in the river water. Most of the measured parameters exhibit a relatively lower concentration in the post-monsoon as compared to pre-monsoon season. The water chemistry highlights the influence of continental weathering aided by secondary contributions from ground water, saline/alkaline soils and anthropogenic activities in the catchment. Results also reflect the dominance of carbonate weathering over silicate weathering in controlling water composition. The Son River delivers about 4.2 million tons of dissolved loads annually to the Ganga River, which accounts for ∼6% of the total annual load carried by the Ganga River to the Bay of Bengal. The average CDR of the Son River is 59.5 tons km−2 yr−1, which is less than the reported 72 tons km−2 yr−1 of the Ganga River and higher than the global average of 36 tons km−2 yr−1. The water chemistry for the pre-monsoon and post-monsoon periods shows a strong seasonal control on solute flux and CDR values. The water chemistry indicates that the Son River water is good to excellent in quality for irrigation and also suitable for drinking purposes.

  16. An evaluation of design characteristics for the water chemistry for SMART

    Energy Technology Data Exchange (ETDEWEB)

    Choi, B. S.; Kim, J. P.; Kim, H. Y.; Yoon, J. H.; Lee, D. J

    1998-07-01

    SMART does not have boron as a chemical shim using boron and does not operate purification system in power operation. However, the water chemistry applied in SMART still needs to meet the integrity and reliable operation requirements. This report reviews the corrosion resistance of the construction materials for SMART and the chemistry operating parameters qualitatively by comparing with those of PWR. The review shows that the construction materials for SMART, such as titanium alloys for steam generator tube materials and zirconium alloy for fuel cladding have good guarantee the integrity and reliability of the primary circuit and fuel cladding as well as the secondary circuit. This review results can be utilized as input data for SMART chemistry design, such as chemistry design guide, and chemistry manual. (author). 25 refs., 8 tabs., 17 figs

  17. Water chemistry of surface waters affected by the Fourmile Canyon wildfire, Colorado, 2010-2011

    Science.gov (United States)

    McCleskey, R. Blaine; Writer, Jeffrey H.; Murphy, Sheila F.

    2012-01-01

    In September 2010, the Fourmile Canyon fire burned about 23 percent of the Fourmile Creek watershed in Boulder County, Colo. Water-quality sampling of Fourmile Creek began within a month after the wildfire to assess its effects on surface-water chemistry. Water samples were collected from five sites along Fourmile Creek (above, within, and below the burned area) monthly during base flow, twice weekly during snowmelt runoff, and at higher frequencies during storm events. Stream discharge was also monitored. Water-quality samples were collected less frequently from an additional 6 sites on Fourmile Creek, from 11 tributaries or other inputs, and from 3 sites along Boulder Creek. The pH, electrical conductivity, temperature, specific ultraviolet absorbance, total suspended solids, and concentrations (dissolved and total) of major cations (calcium, magnesium, sodium, and potassium), anions (chloride, sulfate, alkalinity, fluoride, and bromide), nutrients (nitrate, ammonium, and phosphorus), trace metals (aluminum, arsenic, boron, barium, beryllium, cadmium, cobalt, chromium, copper, iron, mercury, lithium, manganese, molybdenum, nickel, lead, rubidium, antimony, selenium, strontium, vanadium, and zinc), and dissolved organic carbon are here reported for 436 samples collected during 2010 and 2011.

  18. An Environmental Chemistry Experiment: The Determination of Radon Levels in Water.

    Science.gov (United States)

    Welch, Lawrence E.; Mossman, Daniel M.

    1994-01-01

    Describes a radiation experiment developed to complement a new environmental chemistry laboratory curriculum. A scintillation counter is used to measure radon in water. The procedure relies on the fact that toluene will preferentially extract radon from water. Sample preparation is complete in less than 90 minutes. Because the level of…

  19. Water and Life in the International Year of Chemistry

    Science.gov (United States)

    Bernal, Pedro J.

    2011-01-01

    This commentary talks about the worldwide health impact of lack of access to potable water. Household water treatment and storage (HWTS) is described as one approach to improving potable water accessibility in which students and educators can make a contribution to alleviate the problem of lack of access. The author suggests that, as chemists,…

  20. Water chemistry influences the toxicity of silver to the green-lipped mussel Perna viridis.

    Science.gov (United States)

    Vijayavel, Kannappan

    2010-08-01

    The study determined the influence and relative importance of water chemistry parameters (pH, alkalinity, hardness) on the acute toxicity of silver to the green mussel Perna viridis. A preliminary bioassay revealed that 4 mg L(-1) of silver caused 50% mortality (LC50) in 96 h for mussels placed in seawater with pH 8.5, hardness 1,872 mg L(-1), and alkalinity 172 mg L(-1). Mortality of mussels increased with decreasing pH and increasing hardness and alkalinity variables. In contrast the mortality decreased with increasing pH and decreasing hardness and alkalinity values. The water chemistry also affected the concentration of silver in experimental seawater and bioaccumulation of silver in mussels. The results revealed that the chemical properties of seawater must be considered while conducting toxicity tests with metals like silver. The possible explanations for the influence of water chemistry on silver toxicity to P. viridis are discussed.

  1. Radon, volatile organic compounds and water chemistry in springs around Popocatepetl volcano, Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Segovia, N.; Pena, P.; Lopez, M.B.E.; Cisniega, G. [Inst. Nacional de Investigaciones Nucleares, Mexico D.F. (Mexico); Valdes, C.; Armienta, M.A.; Mena, M. [Inst. de Geofisica, UNAM, Ciudad Univ., Mexico D.F. (Mexico)

    2003-07-01

    Popocatepetl volcano is a high-risk active volcano in Central Mexico where the highest population density in the country is settled. Radon in the soil and groundwater together with water chemistry from samples of nearby springs is analysed as a function of the 2002-2003 volcanic activity. Soil radon indicated fluctuations related both to the meteorological and sporadic explosive events. Groundwater radon showed essentially differences in concentration due to the specific characteristics of the studied springs. Water chemistry showed also stability along the monitoring period indicating differences between springs. No anthropogenic pollution from volatile organic compounds was observed. (orig.)

  2. Interstitial water chemistry and nutrients fluxes from tropical intertidal sediment

    Digital Repository Service at National Institute of Oceanography (India)

    Ram, A.; Zingde, M.D.

    downwards with chlorinity. A continuous build-up of NH4 +-N in the interstitial waters unlike other nutrients was evident. Markedly high N:P molar ratios in surficial sections suggested the removal of PO4 3--P from interstitial water. The fluxes of all...

  3. Effects of selected water chemistry variables on copper pitting propagation in potable water

    Energy Technology Data Exchange (ETDEWEB)

    Ha Hung, E-mail: hmh2n@virginia.edu [Center for Electrochemical Science and Engineering, Department of Materials Science and Engineering, University of Virginia, Charlottesville, VA (United States); Taxen, Claes [SWEREA-KIMAB, Stockholm (Sweden); Williams, Keith [Department of Physics, University of Virginia, Charlottesville, VA (United States); Scully, John [Center for Electrochemical Science and Engineering, Department of Materials Science and Engineering, University of Virginia, Charlottesville, VA (United States)

    2011-07-01

    Highlights: > The effects of water composition on pit propagation kinetics on Cu were separated from pit initiation and stabilization using the artificial pit method in a range of dilute HCO{sub 3}{sup -}, SO{sub 4}{sup 2-} and Cl{sup -}-containing waters. > The effective polarization and Ohmic resistance of pits were lower in SO4{sup 2-}-containing solutions and greater in Cl{sup -}-containing solutions. > Relationship between the solution composition and the corrosion product identity and morphology were found. > These, in turn controlled the corrosion product Ohmic resistance and subsequently the pit growth rate. - Abstract: The pit propagation behavior of copper (UNS C11000) was investigated from an electrochemical perspective using the artificial pit method. Pit growth was studied systematically in a range of HCO{sub 3}{sup -}, SO{sub 4}{sup 2-} and Cl{sup -} containing-waters at various concentrations. Pit propagation was mediated by the nature of the corrosion products formed both inside and over the pit mouth (i.e., cap). Certain water chemistry concentrations such as those high in sulfate were found to promote fast pitting that could be sustained over long times at a fixed applied potential but gradually stifled in all but the lowest concentration solutions. In contrast, Cl{sup -} containing waters without sulfate ions resulted in slower pit growth and eventual repassivation. These observations were interpreted through understanding of the identity, amount and porosity of corrosion products formed inside and over pits. These factors controlled their resistive nature as characterized using electrochemical impedance spectroscopy. A finite element model (FEM) was developed which included copper oxidation kinetics, transport by migration and diffusion, Cu(I) and Cu(II) solid corrosion product formation and porosity governed by equilibrium thermodynamics and a saturation index, as well as pit current and depth of penetration. The findings of the modeling were

  4. Analytical chemistry in water quality monitoring during manned space missions

    Science.gov (United States)

    Artemyeva, Anastasia A.

    2016-09-01

    Water quality monitoring during human spaceflights is essential. However, most of the traditional methods require sample collection with a subsequent ground analysis because of the limitations in volume, power, safety and gravity. The space missions are becoming longer-lasting; hence methods suitable for in-flight monitoring are demanded. Since 2009, water quality has been monitored in-flight with colorimetric methods allowing for detection of iodine and ionic silver. Organic compounds in water have been monitored with a second generation total organic carbon analyzer, which provides information on the amount of carbon in water at both the U.S. and Russian segments of the International Space Station since 2008. The disadvantage of this approach is the lack of compound-specific information. The recently developed methods and tools may potentially allow one to obtain in-flight a more detailed information on water quality. Namely, the microanalyzers based on potentiometric measurements were designed for online detection of chloride, potassium, nitrate ions and ammonia. The recent application of the current highly developed air quality monitoring system for water analysis was a logical step because most of the target analytes are the same in air and water. An electro-thermal vaporizer was designed, manufactured and coupled with the air quality control system. This development allowed for liberating the analytes from the aqueous matrix and further compound-specific analysis in the gas phase.

  5. Sterilization Resistance of Bacterial Spores Explained with Water Chemistry.

    Science.gov (United States)

    Friedline, Anthony W; Zachariah, Malcolm M; Middaugh, Amy N; Garimella, Ravindranath; Vaishampayan, Parag A; Rice, Charles V

    2015-11-01

    Bacterial spores can survive for long periods without nutrients and in harsh environmental conditions. This survival is influenced by the structure of the spore, the presence of protective compounds, and water retention. These compounds, and the physical state of water in particular, allow some species of bacterial spores to survive sterilization schemes with hydrogen peroxide and UV light. The chemical nature of the spore core and its water has been a subject of some contention and the chemical environment of the water impacts resistance paradigms. Either the spore has a glassy core, where water is immobilized along with other core components, or the core is gel-like with mobile water diffusion. These properties affect the movement of peroxide and radical species, and hence resistance. Deuterium solid-state NMR experiments are useful for examining the nature of the water inside the spore. Previous work in our lab with spores of Bacillus subtilis indicate that, for spores, the core water is in a more immobilized state than expected for the gel-like core theory, suggesting a glassy core environment. Here, we report deuterium solid-state NMR observations of the water within UV- and peroxide-resistant spores from Bacillus pumilus SAFR-032. Variable-temperature NMR experiments indicate no change in the line shape after heating to 50 °C, but an overall decrease in signal after heating to 100 °C. These results show glass-like core dynamics within B. pumilus SAFR-032 that may be the potential source of its known UV-resistance properties. The observed NMR traits can be attributed to the presence of an exosporium containing additional labile deuterons that can aid in the deactivation of sterilizing agents.

  6. Cloud water chemistry and the production of sulfates in clouds

    Science.gov (United States)

    Hegg, D. A.; Hobbs, P. V.

    1981-01-01

    Measurements are presented of the pH and ionic content of water collected in clouds over western Washington and the Los Angeles Basin. Evidence for sulfate production in some of the clouds is presented. Not all of the sulfur in the cloud water was in the form of sulfate. However, the measurements indicate that the production of sulfate in clouds is of considerable significance in the atmosphere. Comparison of field measurements with model results show reasonable agreement and suggest that the production of sulfate in cloud water is a consequence of more than one conversion mechanism.

  7. SPENT NUCLEAR FUEL STORAGE BASIN WATER CHEMISTRY: ELECTROCHEMICAL EVALUATION OF ALUMINUM CORROSION

    Energy Technology Data Exchange (ETDEWEB)

    Hathcock, D

    2007-10-30

    The factors affecting the optimal water chemistry of the Savannah River Site spent fuel storage basin must be determines in order to optimize facility efficiency, minimize fuel corrosion, and reduce overall environmental impact from long term spent nuclear fuel storage at the Savannah River Site. The Savannah River National Laboratory is using statistically designed experiments to study the effects of NO{sub 3}{sup -}, SO{sub 4}{sup 2-}, and Cl{sup -} concentrations on alloys commonly used not only as fuel cladding, but also as rack construction materials The results of cyclic polarization pitting and corrosion experiments on samples of Al 6061 and 1100 alloys will be used to construct a predictive model of the basin corrosion and its dependence on the species in the basin. The basin chemistry model and corrosion will be discussed in terms of optimized water chemistry envelope and minimization of cladding corrosion.

  8. Results of ground-water, surface-water, and water-chemistry monitoring, Black Mesa area, northeastern Arizona, 1994

    Science.gov (United States)

    Littin, G.R.; Monroe, S.A.

    1995-01-01

    The Black Mesa monitoring program is designed to document long-term effects of ground-water pumping from the N aquifer by industrial and municipal users. The N aquifer is the major source of water in the 5,400-square-mile Black Mesa area, and the ground water occurs under confined and unconfined conditions. Monitoring activities include continuous and periodic measurements of (1) ground-water pumpage from the confined and unconfined areas of the aquifer, (2) ground-water levels in the confined and unconfined areas of the aquifer, (3) surface-water discharge, and (4) chemistry of the ground water and surface water. In 1994, ground-water withdrawals for industrial and municipal use totaled about 7,000 acre-feet, which is an 8-percent increase from the previous year. Pumpage from the confined part of the aquifer increased by about 9 percent to 5,400 acre-feet, and pumpage from the unconfined part of the aquifer increased by about 2 percent to 1,600 acre-feet. Water-level declines in the confined area during 1994 were recorded in 10 of 16 wells, and the median change was a decline of about 2.3 feet as opposed to a decline of 3.3 feet for the previous year. The median change in water levels in the unconfined area was a rise of 0.1 foot in 1994 as opposed to a decline of 0.5 foot in 1993. Measured low-flow discharge along Moenkopi Wash decreased from 3.0 cubic feet per second in 1993 to 2.9 cubic feet per second in 1994. Eleven low-flow measurements were made along Laguna Creek between Tsegi, Arizona, and Chinle Wash to determine the amount of discharge that would occur as seepage from the N aquifer under optimal base-flow conditions. Discharge was 5.6 cubic feet per second near Tsegi and 1.5 cubic feet per second above the confluence with Chinle Wash. Maximum discharge was 5.9 cubic feet per second about 4 miles upstream from Dennehotso. Discharge was measured at three springs. The changes in discharge at Burro and Whisky Springs were small and within the uncertainty of

  9. Chemistry of snow and lake water in Antarctic region

    Indian Academy of Sciences (India)

    Kaushar Ali; Sunil Sonbawane; D M Chate; Devendraa Siingh; P S P Rao; P D Safai; K B Budhavant

    2010-12-01

    Surface snow and lake water samples were collected at different locations around Indian station at Antarctica, Maitri, during December 2004-March 2005 and December 2006-March 2007.Samples were analyzed for major chemical ions. It is found that average pH value of snow is 6.1. Average pH value of lake water with low chemical content is 6.2 and of lake water with high chemical content is 6.5.The Na+ and Cl− are the most abundantly occurring ions at Antarctica. Considerable amount of SO$^{2-}_{4}$ is also found in the surface snow and the lake water which is attributed to the oxidation of DMS produced by marine phytoplankton.Neutralization of acidic components of snow is mainly done by NH$^{+}_{4}$ and Mg2+. The Mg2+, Ca2+ and K+ are nearly equally effective in neutralizing the acidic components in lake water.The NH$^{+}_{4}$ and SO$^{2-}_{4}$ occur over the Antarctica region mostly in the form of (NH4)2SO4.

  10. Removal of sediment and bacteria from water using green chemistry.

    Science.gov (United States)

    Buttice, Audrey L; Stroot, Joyce M; Lim, Daniel V; Stroot, Peter G; Alcantar, Norma A

    2010-05-01

    Although nearly all newly derived water purification methods have improved the water quality in developing countries, few have been accepted and maintained for long-term use. Field studies indicate that the most beneficial methods use indigenous resources, as they are both accessible and accepted by communities they help. In an effort to implement a material that will meet community needs, two fractions of mucilage gum were extracted from the Opuntia ficus-indica cactus and tested as flocculation agents against sediment and bacterial contamination. As diatomic ions are known to affect both mucilage and promote cell aggregation, CaCl(2) was studied in conjunction and compared with mucilage as a bacteria removal method. To evaluate performance, ion-rich waters that mimic natural water bodies were prepared. Column tests containing suspensions of the sediment kaolin exhibited particle flocculation and settling rates up to 13.2 cm/min with mucilage versus control settling rates of 0.5 cm/min. Bacillus cereus tests displayed flocculation and improved settling times with mucilage concentrations lower than 5 ppm and removal rates between 97 and 98% were observed for high bacteria concentration tests (>10(8) cells/ml). This natural material not only displays water purification abilities, but it is also affordable, renewable and readily available.

  11. Coagulation chemistries for silica removal from cooling tower water.

    Energy Technology Data Exchange (ETDEWEB)

    Nyman, May Devan; Altman, Susan Jeanne; Stewart, Tom

    2010-02-01

    The formation of silica scale is a problem for thermoelectric power generating facilities, and this study investigated the potential for removal of silica by means of chemical coagulation from source water before it is subjected to mineral concentration in cooling towers. In Phase I, a screening of many typical as well as novel coagulants was carried out using concentrated cooling tower water, with and without flocculation aids, at concentrations typical for water purification with limited results. In Phase II, it was decided that treatment of source or make up water was more appropriate, and that higher dosing with coagulants delivered promising results. In fact, the less exotic coagulants proved to be more efficacious for reasons not yet fully determined. Some analysis was made of the molecular nature of the precipitated floc, which may aid in process improvements. In Phase III, more detailed study of process conditions for aluminum chloride coagulation was undertaken. Lime-soda water softening and the precipitation of magnesium hydroxide were shown to be too limited in terms of effectiveness, speed, and energy consumption to be considered further for the present application. In Phase IV, sodium aluminate emerged as an effective coagulant for silica, and the most attractive of those tested to date because of its availability, ease of use, and low requirement for additional chemicals. Some process optimization was performed for coagulant concentration and operational pH. It is concluded that silica coagulation with simple aluminum-based agents is effective, simple, and compatible with other industrial processes.

  12. Understanding the interplay between water chemistry and electrochemical properties of copper

    Science.gov (United States)

    Cong, Hongbo

    The pitting behavior of UNS C11000 copper was investigated in a synthetic potable water found to cause pitting using both driven electrochemical methods and under natural conditions at OCP. The latter was monitored with coupled multi-electrode arrays (CMEA). Tests were also conducted in several HCO 3-, SO42- and Cl- containing-waters with systematic variations in the concentrations of these species. Empirical equations that forecast pitting (EPit) and repassivation (ERp) potential as a function of selected water chemistry variables were developed. OCP was a strong function of water chemistry, pH and time. Maximum OCPs were found to increase with both pH and Cl2. Empirical equations that forecast the OCP as a function of pH and Cl2 were also developed. Natural pitting was tested in different pH synthetic waters (6-10) at various Cl2 levels (0-5 ppm). The CMEA method successfully detected the formation of persistent anodes (pitting sites) in pH ≥7 synthetic waters compared to formation of switchable anodes at pH 6. A pitting factor was determined as a function of water chemistry. Pit events were statistically analyzed and potential excursions were compared to EPit and E Rp. Natural pitting events occurred on a percentage of electrodes once the OCP rose above ERp and this could be rationalized based on the statistical spread in EPit. Pits stopped growing once the OCP dropped below ERp Pitting severity increased with Cl2 level and pH. The cathodic capacity of adjacent cathodic sites as a function of water chemistry and the nature of the cathodic sites was also factored into this analysis. Lastly, the possible roles of deposited aluminum solids in pit initiation were also examined using several diagnostic methods.

  13. Photocatalytic water splitting with acridine dyes: Guidelines from computational chemistry

    Science.gov (United States)

    Liu, Xiaojun; Karsili, Tolga N. V.; Sobolewski, Andrzej L.; Domcke, Wolfgang

    2016-01-01

    The photocatalytic splitting of water into Hrad and OHrad radicals in hydrogen-bonded chromophore-water complexes has been explored with computational methods for the chromophores acridine orange (AO) and benzacridine (BA). These dyes are strong absorbers within the range of the solar spectrum. It is shown that low-lying charge-transfer excited states exist in the hydrogen-bonded AOsbnd H2O and BAsbnd H2O complexes which drive the transfer of a proton from water to the chromophore, which results in AOHradsbnd OHrad or BAHradsbnd OHrad biradicals. The AOHrad and BAHrad radicals possess bright ππ∗ excited states with vertical excitation energies near 3.0 eV which are predissociated by a low-lying repulsive πσ∗ state. The conical intersections of the πσ∗ state with the ππ∗ excited states and the ground state provide a mechanism for the photodetachment of the H-atom by a second photon. Our results indicate that AO and BA are promising chromophores for water splitting with visible light.

  14. Integrating Biology, Chemistry, and Mathematics to Evaluate Global Water Problems

    Science.gov (United States)

    Kosal, Erica; Lawrence, Carol; Austin, Rodney

    2010-01-01

    An interdisciplinary and context-driven course focused on global water issues was developed and taught at the college level. Students designed a semester-long research project, collected and analyzed data, and ultimately presented their results and conclusions to the larger community. As a result of the course, students' science literacy improved…

  15. Ground-Water, Surface-Water, and Water-Chemistry Data, Black Mesa Area, Northeastern Arizona - 2006-07

    Science.gov (United States)

    Truini, Margot; Macy, J.P.

    2008-01-01

    The N aquifer is the major source of water in the 5,400 square-mile Black Mesa area in northeastern Arizona. Availability of water is an important issue in northeastern Arizona because of continued water requirements for industrial and municipal use and the needs of a growing population. Precipitation in the Black Mesa area is typically about 6 to 14 inches per year. The water-monitoring program in the Black Mesa area began in 1971 and is designed to provide information about the long-term effects of ground-water withdrawals from the N aquifer for industrial and municipal uses. This report presents results of data collected for the monitoring program in the Black Mesa area from January 2006 to September 2007. The monitoring program includes measurements of (1) ground-water withdrawals, (2) ground-water levels, (3) spring discharge, (4) surface-water discharge, and (5) ground-water chemistry. Periodic testing of ground-water withdrawal meters is completed every 4 to 5 years. The Navajo Tribal Utility Authority (NTUA) yearly totals for the ground-water metered withdrawal data were unavailable in 2006 due to an up-grade within the NTUA computer network. Because NTUA data is often combined with Bureau of Indian Affairs data for the total withdrawals in a well system, withdrawals will not be published in this year's annual report. From 2006 to 2007, annually measured water levels in the Black Mesa area declined in 3 of 11 wells measured in the unconfined areas of the N aquifer, and the median change was 0.0 feet. Measurements indicated that water levels declined in 8 of 17 wells measured in the confined area of the aquifer. The median change for the confined area of the aquifer was 0.2 feet. From the prestress period (prior to 1965) to 2007, the median water-level change for 30 wells was -11.1 feet. Median water-level changes were 2.9 feet for 11 wells measured in the unconfined areas and -40.2 feet for 19 wells measured in the confined area. Spring flow was measured

  16. A spatial and seasonal assessment of river water chemistry across North West England.

    Science.gov (United States)

    Rothwell, J J; Dise, N B; Taylor, K G; Allott, T E H; Scholefield, P; Davies, H; Neal, C

    2010-01-15

    This paper presents information on the spatial and seasonal patterns of river water chemistry at approximately 800 sites in North West England based on data from the Environment Agency regional monitoring programme. Within a GIS framework, the linkages between average water chemistry (pH, sulphate, base cations, nutrients and metals) catchment characteristics (topography, land cover, soil hydrology, base flow index and geology), rainfall, deposition chemistry and geo-spatial information on discharge consents (point sources) are examined. Water quality maps reveal that there is a clear distinction between the uplands and lowlands. Upland waters are acidic and have low concentrations of base cations, explained by background geological sources and land cover. Localised high concentrations of metals occur in areas of the Cumbrian Fells which are subjected to mining effluent inputs. Nutrient concentrations are low in the uplands with the exception sites receiving effluent inputs from rural point sources. In the lowlands, both past and present human activities have a major impact on river water chemistry, especially in the urban and industrial heartlands of Greater Manchester, south Lancashire and Merseyside. Over 40% of the sites have average orthophosphate concentrations >0.1mg-Pl(-1). Results suggest that the dominant control on orthophosphate concentrations is point source contributions from sewage effluent inputs. Diffuse agricultural sources are also important, although this influence is masked by the impact of point sources. Average nitrate concentrations are linked to the coverage of arable land, although sewage effluent inputs have a significant effect on nitrate concentrations. Metal concentrations in the lowlands are linked to diffuse and point sources. The study demonstrates that point sources, as well as diffuse sources, need to be considered when targeting measures for the effective reduction in river nutrient concentrations. This issue is clearly important

  17. Relations between topography, wetlands, vegetation cover and stream water chemistry in boreal headwater catchments in Sweden

    Directory of Open Access Journals (Sweden)

    J.-O. Andersson

    2008-05-01

    Full Text Available A large part of the spatial variation of stream water chemistry is found in headwater streams and small catchments. To understand the dominant processes, taking place in small and heterogeneous catchments, spatial and temporal data with high resolution is needed. In most cases available map data has too low quality and resolution to successfully be used in environmental assessments and modelling. In this study 18 forested catchments (1–4 km2 were selected within a 120×50 km area in the county of Värmland in western Sweden. The aim was to test if topographic and vegetation variables derived from official datasets were correlated to stream water chemistry, represented by DOC, Al, Fe and Si content. A GIS was used to analyse the elevation characteristics, generate topographic indices and calculate the percentage of wetlands and a number of vegetation classes. The results clearly show that the topography has a major influence on the occurrence of wetlands, which has a major influence on stream water chemistry. There were very strong correlations between mean slope and percentage wetland, percentage wetland and DOC, mean slope and DOC and mean topographic wetness index and DOC. The conclusion was that official topographic data, despite uncertain or low quality and resolution, could be useful in the prediction of headwater chemistry in boreal forested catchments.

  18. Governing chemistry of cellulose hydrolysis in supercritical water.

    Science.gov (United States)

    Cantero, Danilo A; Bermejo, M Dolores; Cocero, M José

    2015-03-01

    At extremely low reaction times (0.02 s), cellulose was hydrolyzed in supercritical water (T=400 °C and P=25 MPa) to obtain a sugar yield higher than 95 wt%, whereas the 5-hydroxymethylfurfural (5-HMF) yield was lower than 0.01 wt %. If the reaction time was increased to 1 s, the main product was glycolaldehyde (60 wt%). Independently of the reaction time, the yield of 5-HMF was always lower than 0.01 wt%. To evaluate the reaction mechanism of biomass hydrolysis in pressurized water, several parameters (temperature, pressure, reaction time, and reaction medium) were studied for different biomasses (cellulose, glucose, fructose, and wheat bran). It was found that the H(+) and OH(-) ion concentration in the reaction medium as a result of water dissociation is the determining factor in the selectivity. The reaction of glucose isomerization to fructose and the further dehydration to 5-HMF are highly dependent on the ion concentration. By an increase in the pOH/pH value, these reactions were minimized to allow control of 5-HMF production. Under these conditions, the retroaldol condensation pathway was enhanced, instead of the isomerization/dehydration pathway.

  19. Dominant processes controlling water chemistry of the Pecos River in American southwest

    Science.gov (United States)

    Yuan, Fasong; Miyamoto, Seiichi

    2005-09-01

    Here we show an analysis of river flow and water chemistry data from eleven gauging stations along the Pecos River in eastern New Mexico and western Texas, with time spanning 1959-2002. Analysis of spatial relationship between the long-term average flow and total dissolved solids (TDS) concentration allows us to illuminate four major processes controlling river chemistry, namely saline water addition, evaporative concentration with salt gain or loss, dilution with salt gain or loss, and salt storage. Of the 10 river reaches studied, six reaches exhibit the process dominated by evaporative concentration or freshwater dilution with little change in salt load. Four reaches show considerable salt gains or losses that are induced by surface-ground water interactions. This analysis suggests that the evaporative concentration and freshwater dilution are the prevailing mechanisms, but local processes (e.g., variations in hydrologic flowpath and lithologic formation) also play an important role in regulating the hydrochemistry of the Pecos River.

  20. Kinugasa reactions in water: from green chemistry to bioorthogonal labelling.

    Science.gov (United States)

    Chigrinova, Mariya; MacKenzie, Douglas A; Sherratt, Allison R; Cheung, Lawrence L W; Pezacki, John Paul; Pezacki, Paul

    2015-04-16

    The Kinugasa reaction has become an efficient method for the direct synthesis of β-lactams from substituted nitrones and copper(I) acetylides. In recent years, the reaction scope has been expanded to include the use of water as the solvent, and with micelle-promoted [3+2] cycloadditions followed by rearrangement furnishing high yields of β-lactams. The high yields of stable products under aqueous conditions render the modified Kinugasa reaction amenable to metabolic labelling and bioorthogonal applications. Herein, the development of methods for use of the Kinugasa reaction in aqueous media is reviewed, with emphasis on its potential use as a bioorthogonal coupling strategy.

  1. Kinugasa Reactions in Water: From Green Chemistry to Bioorthogonal Labelling

    Directory of Open Access Journals (Sweden)

    Mariya Chigrinova

    2015-04-01

    Full Text Available The Kinugasa reaction has become an efficient method for the direct synthesis of β-lactams from substituted nitrones and copper(I acetylides. In recent years, the reaction scope has been expanded to include the use of water as the solvent, and with micelle-promoted [3+2] cycloadditions followed by rearrangement furnishing high yields of β-lactams. The high yields of stable products under aqueous conditions render the modified Kinugasa reaction amenable to metabolic labelling and bioorthogonal applications. Herein, the development of methods for use of the Kinugasa reaction in aqueous media is reviewed, with emphasis on its potential use as a bioorthogonal coupling strategy.

  2. Vertical Gradients in Water Chemistry and Age in the Northern High Plains Aquifer, Nebraska, 2003

    Science.gov (United States)

    McMahon, P.B.; Böhlke, J.K.; Carney, C.P.

    2007-01-01

    The northern High Plains aquifer is the primary source of water used for domestic, industrial, and irrigation purposes in parts of Colorado, Kansas, Nebraska, South Dakota, and Wyoming. Despite the aquifer's importance to the regional economy, fundamental ground-water characteristics, such as vertical gradients in water chemistry and age, remain poorly defined. As part of the U.S. Geological Survey's National Water-Quality Assessment Program, water samples from nested, short-screen monitoring wells installed in the northern High Plains aquifer were analyzed for major ions, nutrients, trace elements, dissolved organic carbon, pesticides, stable and radioactive isotopes, dissolved gases, and other parameters to evaluate vertical gradients in water chemistry and age in the aquifer. Chemical data and tritium and radiocarbon ages show that water in the aquifer was chemically and temporally stratified in the study area, with a relatively thin zone of recently recharged water (less than 50 years) near the water table overlying a thicker zone of older water (1,800 to 15,600 radiocarbon years). In areas where irrigated agriculture was an important land use, the recently recharged ground water was characterized by elevated concentrations of major ions and nitrate and the detection of pesticide compounds. Below the zone of agricultural influence, major-ion concentrations exhibited small increases with depth and distance along flow paths because of rock/water interactions. The concentration increases were accounted for primarily by dissolved calcium, sodium, bicarbonate, sulfate, and silica. In general, the chemistry of ground water throughout the aquifer was of high quality. None of the approximately 90 chemical constituents analyzed in each sample exceeded primary drinking-water standards. Mass-balance models indicate that changes in ground-water chemistry along flow paths in the aquifer can be accounted for by small amounts of feldspar and calcite dissolution; goethite and

  3. Spatiotemporal dynamics of spring and stream water chemistry in a high-mountain area

    Energy Technology Data Exchange (ETDEWEB)

    Zelazny, Miroslaw, E-mail: miroslaw.zelazny@uj.edu.pl [Jagiellonian University, Institute of Geography and Spatial Management, Department of Hydrology, 7 Gronostajowa Str., 30-387 Cracow (Poland); Astel, Aleksander, E-mail: astel@apsl.edu.pl [Environmental Chemistry Research Unit, Biology and Environmental Protection Institute, Pomeranian Academy, 22a Arciszewskiego Str., Slupsk, 76-200 (Poland); Wolanin, Anna [Jagiellonian University, Institute of Geography and Spatial Management, Department of Hydrology, 7 Gronostajowa Str., 30-387 Cracow (Poland); Malek, Stanislaw, E-mail: rlmalek@cyf-kr.edu.pl [Department of Forest Ecology, Forest Faculty, Agricultural University of Cracow, 46 29 Listopada Ave., Cracow, 31-425 (Poland)

    2011-05-15

    The present study deals with the application of the self-organizing map (SOM) technique in the exploration of spatiotemporal dynamics of spring and stream water samples collected in the Chocholowski Stream Basin located in the Tatra Mountains (Poland). The SOM-based classification helped to uncover relationships between physical and chemical parameters of water samples and factors determining the quality of water in the studied high-mountain area. In the upper part of the Chocholowski Stream Basin, located on the top of the crystalline core of the Tatras, concentrations of the majority of ionic substances were the lowest due to limited leaching. Significantly higher concentration of ionic substances was detected in spring and stream samples draining sedimentary rocks. The influence of karst-type springs on the quality of stream water was also demonstrated. - Highlights: > We use SOM approach to explore physiochemical data for mountain waters. > Geologic structure and hydrological events impact water chemistry. > Limited leaching, typical of crystalline core, reflects in low water mineralization. > Sedimentary rocks are susceptible for leaching. > Eutrophication has not been shown to be a threat in the Chocholowska Valley. - Spatiotemporal dynamics of spring and stream water chemistry in unique high-mountain area was evaluated by the self-organizing map technique.

  4. Geohydrological characterization, water-chemistry, and ground-water flow simulation model of the Sonoma Valley area, Sonoma County, California

    Science.gov (United States)

    Farrar, Christopher D.; Metzger, Loren F.; Nishikawa, Tracy; Koczot, Kathryn M.; Reichard, Eric G.; Langenheim, V.E.

    2006-01-01

    The Sonoma Valley, located about 30 miles north of San Francisco, is one of several basins in Sonoma County that use a combination of ground water and water delivered from the Russian River for supply. Over the past 30 years, Sonoma Valley has experienced rapid population growth and land-use changes. In particular, there has been a significant increase in irrigated agriculture, predominantly vineyards. To provide a better understanding of the ground-water/surface-water system in Sonoma Valley, the U.S. Geological Survey compiled and evaluated existing data, collected and analyzed new data, and developed a ground-water flow model to better understand and manage the ground-water system. The new data collected include subsurface lithology, gravity measurements, groundwater levels, streamflow gains and losses, temperature, water chemistry, and stable isotopes. Sonoma Valley is drained by Sonoma Creek, which discharges into San Pablo Bay. The long-term average annual volume of precipitation in the watershed is estimated to be 269,000 acre-feet. Recharge to the ground-water system is primarily from direct precipitation and Sonoma Creek. Discharge from the ground-water system is predominantly outflow to Sonoma Creek, pumpage, and outflow to marshlands and to San Pablo Bay. Geologic units of most importance for groundwater supply are the Quaternary alluvial deposits, the Glen Ellen Formation, the Huichica Formation, and the Sonoma Volcanics. In this report, the ground-water system is divided into three depth-based geohydrologic units: upper (less than 200 feet below land surface), middle (between 200 and 500 feet), and lower (greater than 500 feet). Synoptic streamflow measurements were made along Sonoma Creek and indicate those reaches with statistically significant gains or losses. Changes in ground-water levels in wells were analyzed by comparing historical contour maps with the contour map for 2003. In addition, individual hydrographs were evaluated to assess temporal

  5. Water-stable fac-{TcO₃}⁺ complexes - a new field of technetium chemistry.

    Science.gov (United States)

    Braband, Henrik

    2011-01-01

    The development of technetium chemistry has been lagging behind that of its heavier congener rhenium, primarily because the inherent radioactivity of all Tc isotopes has limited the number of laboratories that can study the chemistry of this fascinating element. Although technetium is an artificial element, it is not rare. Significant amounts of the isotope (99)Tc are produced every day as a fission byproduct in nuclear power plants. Therefore, a fundamental understanding of the chemistry of (99)Tc is essential to avoid its release into the environment. In this article the chemistry of technetium at its highest oxidation state (+VII) is reviewed with a special focus on recent developments which make water-stable complexes of the general type [TcO(3)(tacn-R)](+) (tacn-R = 1,4,7-triazacyclononane or derivatives) accessible. Complexes containing the fac-{TcO(3)}(+) core display a unique reactivity. In analogy to [OsO(4)] and [RuO(4)], complexes containing the fac-{TcO(3)}(+) core undergo with alkenes metal-mediated, vicinal cis-dihydroxylation reactions (alkene-glycol interconversion) in water via a (3+2)-cycloaddition reaction. Therefore, water-stable fac-{(99m)TcO(3)}(+) complexes pave the way for a new labeling strategy for radiopharmaceutical applications, based on (3+2)-cycloaddition reactions. This new concept for the labeling of biomolecules with small [(99m)TcO(3)(tacn-R)](+)-type complexes by way of a (3+2)-cycloaddition with alkenes is discussed in detail. The herein reported developments in high-valent technetium chemistry create a new field of research with this artificial element. This demonstrates the potential of fundamental research to provide new impetus of innovation for the development of new methods for radiopharmaceutical applications.

  6. On the pore water chemistry effect on spectral induced polarization measurements in the presence of pyrite

    Science.gov (United States)

    Placencia-Gómez, Edmundo; Slater, Lee D.

    2016-12-01

    In order to expand the application of the induced polarization (IP) method as a technique for monitoring metallic mineral dissolution and precipitation mechanisms, we studied the effects of variations in pore water chemistry on the spectral induced polarization (SIP) response of a mixture of silica-sand and pyrite particles in the laboratory. We investigated the dependence of the SIP response on both pore water conductivity and pH for various chemical compositions: redox-passive (P) versus redox-active (A) ions, using CaCl2 as P-ions, and FeSO4 and FeCl3 as A-ion brines. The effect of pore water chemistry was evaluated by means of a recently proposed volumetric specific capacitance model. The SIP response (IP-effect) was primarily determined by the pore water conductivity and the specific capacitance was only weakly dependent on the chemical composition and pHw. We found that the specific capacitance varies to first order over a limited range and approximates a single value (≈ 302 F m- 3 in average). However, variations in the specific capacitance as a function of active versus inactive ion chemistry might be important to consider when using IP to monitor specific mineral dissolution and precipitation processes.

  7. Simulation of stratospheric water vapor trends: impact on stratospheric ozone chemistry

    Directory of Open Access Journals (Sweden)

    A. Stenke

    2005-01-01

    Full Text Available A transient model simulation of the 40-year time period 1960 to 1999 with the coupled climate-chemistry model (CCM ECHAM4.L39(DLR/CHEM shows a stratospheric water vapor increase over the last two decades of 0.7 ppmv and, additionally, a short-term increase after major volcanic eruptions. Furthermore, a long-term decrease in global total ozone as well as a short-term ozone decline in the tropics after volcanic eruptions are modeled. In order to understand the resulting effects of the water vapor changes on lower stratospheric ozone chemistry, different perturbation simulations were performed with the CCM ECHAM4.L39(DLR/CHEM feeding the water vapor perturbations only to the chemistry part. Two different long-term perturbations of lower stratospheric water vapor, +1 ppmv and +5 ppmv, and a short-term perturbation of +2 ppmv with an e-folding time of two months were applied. An additional stratospheric water vapor amount of 1 ppmv results in a 5–10% OH increase in the tropical lower stratosphere between 100 and 30 hPa. As a direct consequence of the OH increase the ozone destruction by the HOx cycle becomes 6.4% more effective. Coupling processes between the HOx-family and the NOx/ClOx-family also affect the ozone destruction by other catalytic reaction cycles. The NOx cycle becomes 1.6% less effective, whereas the effectiveness of the ClOx cycle is again slightly enhanced. A long-term water vapor increase does not only affect gas-phase chemistry, but also heterogeneous ozone chemistry in polar regions. The model results indicate an enhanced heterogeneous ozone depletion during antarctic spring due to a longer PSC existence period. In contrast, PSC formation in the northern hemisphere polar vortex and therefore heterogeneous ozone depletion during arctic spring are not affected by the water vapor increase, because of the less PSC activity. Finally, this study shows that 10% of the global total ozone decline in the transient model run

  8. Design study of water chemistry control system for IASCC irradiation test

    Energy Technology Data Exchange (ETDEWEB)

    Mori, Yuichiro; Ide, Hiroshi; Nabeya, Hideaki [Japan Atomic Energy Research Inst., Oarai, Ibaraki (Japan). Oarai Research Establishment; Tsukada, Takashi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    2002-02-01

    In relation to the aging of Light Water Reactor (LWR), the Irradiation Assisted Stress Corrosion Cracking (IASCC) has been regarded as a significant and urgent issue for the reliability of in-core components of LWR, and the irradiation research on the IASCC is now under schedule. With the progress of the irradiation research on reactor materials, well-controlled environment conditions during irradiation testing are required. Especially for irradiation testing of IASCC studies, water chemistry control is essential in addition to the control of neutron fluence and irradiation temperature. According to these requirements, at the Japan Atomic Energy Research Institute (JAERI), an irradiation testing facility that simulates in-core environment of Boiling Water Reactor (BWR) has been designed to be installed in the Japan Materials Testing Reactor (JMTR). This facility is composed of the Saturated Temperature Capsules (SATCAP) that are installed into the JMTR's core to irradiate material specimens, the Water Control Unit that is able to supply high-temperature and high-pressure chemical controlled water to SATCAP, and other components. This report describes the design study of water chemistry control system of the Water Control Unit. The design work has been performed in the fiscal year 1999. (author)

  9. Introduction of Mass Spectrometry in an First-Semester General Chemistry Laboratory Course: Quantification of Mtbe or Dmso in Water

    Science.gov (United States)

    Solow, Mike

    2004-01-01

    Quantification of a contaminant in water provides the first-year general chemistry students with a tangible application of mass spectrometry. The relevance of chemistry to assessing and solving environmental problems is highlighted for students when they perform mass spectroscopy experiments.

  10. 2015 AAAR Conference Symposium: "The Role of Water in Aerosol Chemistry"

    Energy Technology Data Exchange (ETDEWEB)

    McNeill, V. Faye [Columbia Univ., New York, NY (United States); Weber, Rodney [Georgia Inst. of Technology, Atlanta, GA (United States)

    2015-10-16

    The DOE-sponsored symposium, "The Role of Water in Aerosol Chemistry" was held at the 2015 Annual meeting of AAAR. The funding supported, in part, travel, lodging, and registration expenses for invited symposium speakers, and travel and lodging expenses allowing students to attend and make presentations at a special conference symposium that focuses on topics of interest to the U.S. DOE Atmospheric System Research (ASR) program.

  11. Radon, water chemistry and pollution check by volatile organic compounds in springs around Popocatepetl volcano, Mexico

    OpenAIRE

    Mena, M.; Cisniega, G.; Lopez, B.; M. A. Armienta; Valdés, C; Peña, P.; N. Segovia

    2005-01-01

    Popocatepetl volcano is a high-risk active volcano in Central Mexico where the highest population density in the country is settled. Radon in the soil and groundwater together with water chemistry from samples of nearby springs were analysed as a function of the 2002-2003 volcanic activity. The measurements of soil radon indicated fluctuations related to both the meteorological and sporadic explosive events. Groundwater radon showed essential differences in concentration d...

  12. Organic peroxide and OH formation in aerosol and cloud water: laboratory evidence for this aqueous chemistry

    Directory of Open Access Journals (Sweden)

    Y. B. Lim

    2015-06-01

    Full Text Available Aqueous chemistry in atmospheric waters (e.g., cloud droplets or wet aerosols is well accepted as an atmospheric pathway to produce secondary organic aerosol (SOAaq. Water-soluble organic compounds with small carbon numbers (C2-C3 are precursors for SOAaq and products include organic acids, organic sulfates, and high molecular weight compounds/oligomers. Fenton reactions and the uptake of gas-phase OH radicals are considered to be the major oxidant sources for aqueous organic chemistry. However, the sources and availability of oxidants in atmospheric waters are not well understood. The degree to which OH is produced in the aqueous phase affects the balance of radical and non-radical aqueous chemistry, the properties of the resulting aerosol, and likely its atmospheric behavior. This paper demonstrates organic peroxide formation during aqueous photooxidation of methylglyoxal using ultra high resolution Fourier Transform Ion Cyclotron Resonance electrospray ionization mass spectrometry (FTICR-MS. Organic peroxides are known to form through gas-phase oxidation of volatile organic compounds. They contribute secondary organic aerosol (SOA formation directly by forming peroxyhemiacetals, and epoxides, and indirectly by enhancing gas-phase oxidation through OH recycling. We provide simulation results of organic peroxide/peroxyhemiacetal formation in clouds and wet aerosols and discuss organic peroxides as a source of condensed-phase OH radicals and as a contributor to aqueous SOA.

  13. Wildfires and water chemistry: effect of metals associated with wood ash.

    Science.gov (United States)

    Cerrato, José M; Blake, Johanna M; Hirani, Chris; Clark, Alexander L; Ali, Abdul-Mehdi S; Artyushkova, Kateryna; Peterson, Eric; Bixby, Rebecca J

    2016-08-10

    The reactivity of metals associated with ash from wood collected from the Valles Caldera National Preserve, Jemez Mountains, New Mexico, was assessed through a series of laboratory experiments. Microscopy, spectroscopy, diffraction, and aqueous chemistry measurements were integrated to determine the chemical composition of wood ash and its effect on water chemistry. Climate change has caused dramatic impacts and stresses that have resulted in large-scale increases in wildfire activity in semi-arid areas of the world. Metals and other constituents associated with wildfire ash can be transported by storm event runoff and negatively affect the water quality in streams and rivers. Differences among ash from six tree species based on total concentrations of metals such as Ca, Al, Mg, Fe, and Mn were identified using non-metric multidimensional analysis. Metal-bearing carbonate and oxide phases were quantified by X-ray diffraction analyses and X-ray spectroscopy analyses. These metal-bearing carbonate phases were readily dissolved in the first 30 minutes of reaction with 18 MΩ water and 10 mM HCO3(-) in laboratory batch experiments which resulted in the release of metals and carbonates in the ash, causing water alkalinity to increase. However, metal concentrations decreased over the course of the experiment, suggesting that metals re-adsorb to ash. Our results suggest that the dissolution of metal-bearing carbonate and oxide phases in ash and metal re-adsorption to ash are relevant processes affecting water chemistry after wildfire events. These results have important implications to better understand the impact of wildfire events on water quality.

  14. Hydrogeochemical processes controlling water and dissolved gas chemistry at the Accesa sinkhole (southern Tuscany, central Italy

    Directory of Open Access Journals (Sweden)

    Franco Tassi

    2014-05-01

    Full Text Available The 38.5 m deep Lake Accesa is a sinkhole located in southern Tuscany (Italy that shows a peculiar water composition, being characterized by relatively high total dissolved solids (TDS values (2 g L-1 and a Ca(Mg-SO4 geochemical facies. The presence of significant amounts of extra-atmospheric gases (CO2 and CH4, which increase their concentrations with depth, is also recognized. These chemical features, mimicking those commonly shown by volcanic lakes fed by hydrothermal-magmatic reservoirs, are consistent with those of mineral springs emerging in the study area whose chemistry is produced by the interaction of meteoric-derived waters with Mesozoic carbonates and Triassic evaporites. Although the lake has a pronounced thermocline, water chemistry does not show significant changes along the vertical profile. Lake water balance calculations demonstrate that Lake Accesa has >90% of its water supply from sublacustrine springs whose subterranean pathways are controlled by the local structural assessment that likely determined the sinking event, the resulting funnel-shape being then filled by the Accesa waters. Such a huge water inflow from the lake bottom (~9·106 m3 yr-1 feeds the lake effluent (Bruna River and promotes the formation of water currents, which are able to prevent the establishment of a vertical density gradient. Consequently, a continuous mixing along the whole vertical water column is established. Changes of the drainage system by the deep-originated waters in the nearby former mining district have strongly affected the outflow rates of the local mineral springs; thus, future intervention associated with the ongoing remediation activities should carefully be evaluated to preserve the peculiar chemical features of Lake Accesa.

  15. Hydrogen chloride heterogeneous chemistry on frozen water particles in subsonic aircraft plume. Laboratory studies and modelling

    Energy Technology Data Exchange (ETDEWEB)

    Persiantseva, N.V.; Popovitcheva, O.B.; Rakhimova, T.V. [Moscow State Univ. (Russian Federation)

    1997-12-31

    Heterogeneous chemistry of HCl, as a main reservoir of chlorine content gases, has been considered after plume cooling and ice particle formation. The HCl, HNO{sub 3}, N{sub 2}O{sub 5} uptake efficiencies by frozen water were obtained in a Knudsen-cell flow reactor at the subsonic cruise conditions. The formation of ice particles in the plume of subsonic aircraft is simulated to describe the kinetics of gaseous HCl loss due to heterogeneous processes. It is shown that the HCl uptake by frozen water particles may play an important role in the gaseous HCl depletion in the aircraft plume. (author) 14 refs.

  16. Understanding the Role of Water on Electron-Initiated Processes and Radical Chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Garrett, Bruce C [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Colson, Steven D [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Dixon, David A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Laufer, Allan H [US Department of Energy Office of Science Office of Basic Energy Sciences; Ray, Douglas [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2003-06-10

    On September 26–28, 2002, a workshop entitled “Understanding the Role of Water on Electron-Initiated Processes and Radical Chemistry” was held to assess new research opportunities in electron-driven processes and radical chemistry in aqueous systems. Of particular interest was the unique and complex role that the structure of water plays in influencing these processes. Novel experimental and theoretical approaches to solving long-standing problems in the field were explored. A broad selection of participants from universities and the national laboratories contributed to the workshop, which included scientific and technical presentations and parallel sessions for discussions and report writing.

  17. Steam chemistry - interaction of chemical species with water, steam, and materials during evaporation, superheating, and condensation. Proceedings

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1999-07-01

    Topics of this proceedings are: steam chemistry, supercritical water, effects of chemicals in steam (acetic acid, formic acid, phosphoric acid or other impurities); solubility and deposition, condensation processes and effect of impurities; nucleation; gas-liquid interfaces; steam treatment. (SR)

  18. Assessing Changes in Water Chemistry Along the Mountain to Urban Gradient

    Science.gov (United States)

    Gabor, R. S.; Brooks, P. D.; Neilson, B. T.; Barnes, M. L.; Stout, T.; Millington, M. R.; Gelderloos, A.; Tennant, H.; Eiriksson, D.

    2015-12-01

    Throughout the western US, growing population centers rely on mountain watersheds that are already sensitive to hydrologic stressors. We examined rivers along Utah's Wasatch Front over a range of spatial and discharge scales, confusing on the mountain-to-urban transition to identify how urbanization impacts water resources. The rivers we studied all originate in canyons with impact level ranging from minimal human disturbance to roads and open grazing cattle. Each river enters an urban area after leaving the canyon, where there is significantly more anthropogenic impact on the system. As part of an interdisciplinary effort with the iUTAH project, sample sites were selected at intervals along each river and a variety of measurements were made, including basic water chemistry along with discharge, water isotopes, nutrients, and organic matter analysis. By combining physical and chemical parameters we were able to quantify groundwater influence in gaining reaches and how those differ between the mountain and urban environments. We also identified how the urban system impacted hydrologic and biogeochemical processes in the catchment. For example, in Red Butte Creek discharge tripled through gaining reached in the canyon with only small corresponding changes in conductivity or nitrate levels. However in the urban stretch a gaining reach that tripled the discharge corresponded with a doubling in the conductivity and order of magnitude increase in nitrate. The fact that we first see this change in chemistry during a gaining reach, and not in an area full of storm culverts, suggests that urban impact to stream chemistry predominately occurs through the groundwater. Further work will incorporate ecological and climatic data along with the hydrologic and chemical datasets to identify how controls on water resources change along the mountain to urban gradient. By combining this physical information with sociological data we can identify green infrastructure solutions to

  19. Glycol-Water Interactions and co-existing phases and Temperature Dependent Solubility. An Example Of Carbon-Hydrogen Chemistry In Water

    CERN Document Server

    Michael, Fredrick

    2010-01-01

    Recently there has been great interest in Glycol-Water chemistry and solubility and temperature dependent phase dynamics. The Glycol-Water biochemistry of interactions is present in plant biology and chemistry, is of great interest to chemical engineers and biochemists as it is a paradigm of Carbon-Hydrogen Water organic chemistry. There is an interest moreover in formulating a simpler theory and computation model for the Glycol-Water interaction and phase dynamics, that is not fully quantum mechanical yet has the high accuracy available from a fully quantum mechanical theory of phase transitions of fluids and Fermi systems. Along these lines of research interest we have derived a Lennard-Jones -like theory of interacting molecules-Water in a dissolved adducts of Glycol-Water system interacting by Hydrogen bonds whose validity is supported at the scale of interactions by other independent molecular dynamics investigations that utilize force fields dependent on their experimental fittings to the Lennard-Jones ...

  20. Hydrothermal activity in the Lau back-arc basin: Sulfides and water chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Fouquet, Y.; Charlou, J.L.; Donval, J.P.; Foucher, J.P. (Institut Francais de Recherche et d' Exploitation de la Mer, Plouzane (France)); von Stackelberg, U.; Wiedicke, M. (Bundesanstalt fur Geowissenschaften und Rohstoffe, Hannover (Germany)); Erzinger, J. (Justus-Liebig-Universitat, Giessen (Germany)); Herzig, P. (Rheinish-Westfalische Technische Hochschule, Aachen (Germany)); Muhe, R. (Universitat Kiel (Germany)); Soakai, S. (Ministry of Lands Survey and Natural Resources, Nuku' Alofa (Tonga)); Whitechurch, H. (Ecole et Observatoire de Physique du Globe de Strasbourg (France))

    1991-04-01

    The submersible Nautile completed 22 dives during the Nautilau cruise (R/V Nadir, April 17-May 10, 1989) for a detailed investigation of the southern Lau basin near Tonga. The objective of the scientific team from France, Germany, and Tonga was to understand the process of sea-floor ore formation associated with hydrothermal circulation along the Valu Fa back-arc ridge behind the Tonga-Kermadec trench. The four diving areas, between lat21{degree}25'S and 22{degree}40'S in water{approximately}2000 m deep, were selected on the basis of results from cruises of the R/V Jean Charcot and R/V Sonne. The Nadir cruise provided proof of hydrothermal activity-in all for areas, over more than 100 km-as indicated by the widespread occurence of hydrothermal deposits and by heat flow, conductivity, and temperature measurements near the sea bottom. The most spectacular findings were high-temperature white and black smokers and associated fauna and ore deposits. Hydrothermal water chemistry and sulfide composition data presented here indicate that this hydrothermal field is very different from the hydrothermal fields in oceanic ridges. This difference is seen in water chemistry of the hydrothermal fluid (pH=2 and high metal content) and the chemical composition of sulfides (enrichment in Ba, As, and Pb).

  1. Does water chemistry limit the distribution of New Zealand mud snails in Redwood National Park?

    Science.gov (United States)

    Vazquez, Ryan; Ward, Darren M.; Sepulveda, Adam

    2016-01-01

    New Zealand mud snails (NZMS) are exotic mollusks present in many waterways of the western United States. In 2009, NZMS were detected in Redwood Creek in Redwood National Park, CA. Although NZMS are noted for their ability to rapidly increase in abundance and colonize new areas, after more than 5 years in Redwood Creek, their distribution remains limited to a ca. 300 m reach. Recent literature suggests that low specific conductivity and environmental calcium can limit NZMS distribution. We conducted laboratory experiments, exposing NZMS collected from Redwood Creek to both natural waters and artificial treatment solutions, to determine if low conductivity and calcium concentration limit the distribution of NZMS in Redwood National Park. For natural water exposures, we held NZMS in water from their source location (conductivity 135 μS/cm, calcium 13 mg/L) or water from four other locations in the Redwood Creek watershed encompassing a range of conductivity (77–158 μS/cm) and calcium concentration (4 months) in the lowest conductivity waters from Redwood Creek and all but the lowest-conductivity treatment solutions, regardless of calcium concentration. However, reproductive output was very low in all natural waters and all low-calcium treatment solutions. Our results suggest that water chemistry may inhibit the spread of NZMS in Redwood National Park by reducing their reproductive output.

  2. Temporal variations of geyser water chemistry in the Upper Geyser Basin, Yellowstone National Park, USA

    Science.gov (United States)

    Hurwitz, Shaul; Hunt, Andrew G.; Evans, William C.

    2012-01-01

    Geysers are rare features that reflect a delicate balance between an abundant supply of water and heat and a unique geometry of fractures and porous rocks. Between April 2007 and September 2008, we sampled Old Faithful, Daisy, Grand, Oblong, and Aurum geysers in Yellowstone National Park's Upper Geyser Basin and characterized temporal variations in major element chemistry and water isotopes (δ18O, δD, 3H). We compare these temporal variations with temporal trends of Geyser Eruption Intervals (GEI). SiO2 concentrations and geothermometry indicate that the geysers are fed by waters ascending from a reservoir with temperatures of ∼190 to 210°C. The studied geysers display small and complex chemical and isotopic seasonal variations, and geysers with smaller volume display larger seasonal variations than geysers with larger volumes. Aurum and Oblong Geysers contain detectable tritium concentrations, suggesting that erupted water contains some modern meteoric water. We propose that seasonal GEI variations result from varying degrees of evaporation, meteoric water recharge, water table fluctuations, and possible hydraulic interaction with the adjacent Firehole River. We demonstrate that the concentrations of major dissolved species in Old Faithful Geyser have remained nearly constant since 1884 despite large changes in Old Faithful's eruption intervals, suggesting that no major changes have occurred in the hydrothermal system of the Upper Geyser Basin for >120 years. Our data set provides a baseline for monitoring future changes in geyser activity that might result from varying climate, earthquakes, and changes in heat flow from the underlying magmatic system.

  3. Cumulative soil chemistry changes from land application of saline-sodic waters

    Energy Technology Data Exchange (ETDEWEB)

    Ganjegunte, G.K.; King, L.A.; Vance, G.F. [University of Wyoming, Laramie, WY (United States). Department for Renewable Resources

    2008-09-15

    Management of large volumes (60,000 ha-m) of co-production water associated with coal bed natural gas (CBNG) water extraction is a potential concern in the Powder River Basin (PRB) of Wyoming and Montana due to elevated water salinity and sodicity levels. Land application of saline-sodic CBNG water is a common water management method being practiced in the PRB, which can result in deterioration in soil quality. The objective of this study was to evaluate effects from 1 to 4 yr of land application with CBNG water on soil chemical properties at six study sites (fine to loamy, mixed to smectitic, mesic, Ustic Ardisols and Entisols) in the Wyoming PRB region. Changes in chemistry of soils collected from six depths irrigated with CBNG water were compared with representative non-irrigated soils. Applications of CBNG water significantly increased soil EC, SAR, and ESP values (up to 21, 74, and 24 times, respectively) compared with non-irrigated soils. Differences in soil chemical properties between an irrigated and non-irrigated coarse-textured soil were less than that of fine-textured soils, emphasizing texture as an important factor for salinity buildup. Pretreatment of CBNG water using a sulfur burner and application of gypsum and elemental S soil amendments reduced soil pH but did not prevent the build-up of salts and sodium. Study results suggest that current CBNG water management strategies are not as effective as projected. Additional research is needed to develop management strategies appropriate for mitigating adverse effects of CBNG water irrigation.

  4. Cumulative soil chemistry changes from land application of saline-sodic waters.

    Science.gov (United States)

    Ganjegunte, Girisha K; King, Lyle A; Vance, George F

    2008-01-01

    Management of large volumes (60,000 ha-m) of co-production water associated with coal bed natural gas (CBNG) water extraction is a potential concern in the Powder River Basin (PRB) of Wyoming and Montana due to elevated water salinity and sodicity levels. Land application of saline-sodic CBNG water is a common water management method being practiced in the PRB, which can result in deterioration in soil quality. The objective of this study was to evaluate effects from 1 to 4 yr of land application with CBNG water on soil chemical properties at six study sites (fine to loamy, mixed to smectitic, mesic, Ustic Ardisols and Entisols) in the Wyoming PRB region. Changes in chemistry of soils collected from six depths irrigated with CBNG water were compared with representative nonirrigated soils. Applications of CBNG water significantly increased soil EC, SAR, and ESP values (up to 21, 74, and 24 times, respectively) compared with nonirrigated soils. Differences in soil chemical properties between an irrigated and nonirrigated coarse-textured soil were less than that of fine-textured soils, emphasizing texture as an important factor for salinity buildup. Pretreatment of CBNG water using a sulfur burner and application of gypsum and elemental S soil amendments reduced soil pH but did not prevent the build-up of salts and sodium. Study results suggest that current CBNG water management strategies are not as effective as projected. Additional research is needed to develop management strategies appropriate for mitigating adverse effects of CBNG water irrigation.

  5. Source Water Flow Pathways In Forested, Mountain, Headwater Streams: A Link Between Sediment Movement Patterns And Stream Water Chemistry.

    Science.gov (United States)

    Martin, S.; Conklin, M. H.; Liu, F.

    2015-12-01

    Three years of continuous and discrete sediment and water quality data, from four forested, mountain, headwater catchments in the Sierra Nevada, is used to identify water sources, determine the importance of sub-surface flow pathways, detect any changes in source waters due to seasonal variation or drought, and link flow pathways with observed patterns of in-channel sediment movement within the study watersheds. Patterns in stream chemistry and turbidity point to infiltration as the dominant flow pathway within these catchments. Data support a flow pathway conceptual model in which precipitation water infiltrates into the shallow or deeper subsurface, increasing the hydraulic head of the water table and pushing pre-event water into the stream ahead of event water. Study catchments contain perennial streams and are characterized by a Mediterranean climate with a distinct wet and dry season. Sites are located in the rain-snow transition zone with snow making up 40 to 60 percent of average annual precipitation. Barring human disturbances such as logging/grazing (compaction) or fire (hydrophobicity), catchment soils have high infiltration capacities. Springs and seeps maintain baseflow during the summer low-flow season, and shifting chemical signals within the streams indicate the increased importance of sub-surface water sources during drought years. End-member mixing analysis was conducted to identify possible water end members. Turbidity hysteresis patterns described by previous studies show in-channel sources are dominant for discharge events year round, and there is no difference in fine sediment delivery to streams with or without a soil protecting layer of snow on the land surface. The dominance of sub-surface water sources and evidence for infiltration flow fits with turbidity data, as little material is reaching the stream due to erosive overland flow. An understanding of flow pathways provides a foundation for sustainable land use management in forested

  6. Tectonic, climatic and hydrothermal control on sedimentation and water chemistry of northern Lake Malawi (Nyasa), Tanzania

    Science.gov (United States)

    Branchu, Philippe; Bergonzini, Laurent; Delvaux, Damien; De Batist, Marc; Golubev, Vladimir; Benedetti, Marc; Klerkx, Jean

    2005-11-01

    This paper presents a multi-disciplinary characterisation of processes that influence sedimentation and lake water chemistry in the northern part of the Lake Malawi (or Lake Nyasa), East Africa. This characterisation is based on geophysical (heat-flow), tectonic, hydrological, hydrochemical (major elements, stable isotopes) and sedimentological (seismic profiles, core mineralogy) studies of data acquired from 1990 to 1994 during the CASIMIR project (Comparative Analysis of Sedimentary Infill Mechanisms in Rifts). Sub-surface activity is expressed through seismic and volcanic activity, as well as elevated heat-flow values, both beneath the lake and the surrounding area; hydrothermal activity is observed in the watershed however it was not clearly identified in the sub-lacustrine environment. Relatively high heat-flow values (80-90 mW/m 2) and the chemical composition of hydrothermal fluids in hot springs suggest the presence of a magmatic body at depth. The influence of Quaternary tectonic activity on sedimentary dynamics and infilling is observed not only on land but also in the lake through high-resolution seismic profiles. The main feature is a general tilting of the Kyela Plain as shown by a shift in the river course. The Quaternary stacking pattern of seven sedimentary sequences identified on a grid of high-resolution seismic reflection profiles represents a complete long-term lake-level cycle, from a lake lowstand at about 320 m below the present level to the present-day lake highstand. The North-Kiwira and Songwe River delta systems, composed of a number of stacked lobes, were developed in response to the interplay between gradual lake-level rise, tectonic movement and sediment input. The river dynamics is also recorded in a short core by a mineralogical evolution probably due to a decrease of detrital inputs from the Songwe River in response to hydroclimatic changes. Such changes are very important as this northern part of the watershed is considered as a

  7. Research in Physical Chemistry and Chemical Education: Part A--Water Mediated Chemistry of Oxidized Atmospheric Compounds Part B--The Development of Surveying Tools to Determine How Effective Laboratory Experiments Contribute to Student Conceptual Understanding

    Science.gov (United States)

    Maron, Marta Katarzyna

    2011-01-01

    This dissertation is a combination of two research areas, experimental physical chemistry, Chapters I to V, and chemical education, Chapters VI to VII. Chapters I to V describe research on the water-mediated chemistry of oxidized atmospheric molecules and the impact that water has on the spectra of these environmental systems. The role of water…

  8. Relation of water chemistry of the Edwards aquifer to hydrogeology and land use, San Antonio Region, Texas

    Science.gov (United States)

    Buszka, Paul M.

    1987-01-01

    Water-chemistry data from the Edwards aquifer for 1976-85, consisting of nearly 1,500 chemical analyses from 280 wells and 3 springs, were used to statistically evaluate relations among ground-water chemistry, hydrogeology, and land use. Five land uses associated with sampled wells were classified on the basis of published information and field surveys. Four major subareas of the aquifer were defined to reflect the relative susceptibility of ground water to contamination originating from human activities using hydrogeologic and tritium data.

  9. Chemosensory deprivation in juvenile coho salmon exposed to dissolved copper under varying water chemistry conditions.

    Science.gov (United States)

    McIntyre, Jenifer K; Baldwin, David H; Meador, James P; Scholz, Nathaniel L

    2008-02-15

    Dissolved copper is an important nonpoint source pollutant in aquatic ecosystems worldwide. Copper is neurotoxic to fish and is specifically known to interfere with the normal function of the peripheral olfactory nervous system. However,the influence of water chemistry on the bioavailability and toxicity of copper to olfactory sensory neurons is not well understood. Here we used electrophysiological recordings from the olfactory epithelium of juvenile coho salmon (Oncorhynchus kisutch) to investigate the impacts of copper in freshwaters with different chemical properties. In low ionic strength artificial fresh water, a short-term (30 min) exposure to 20 microg/L dissolved copper reduced the olfactory response to a natural odorant (10(-5) M L-serine) by 82%. Increasing water hardness (0.2-1.6 mM Ca) or alkalinity (0.2-3.2 mM HCO3-) only slightly diminished the inhibitory effects of copper. Moreover, the loss of olfactory function was not affected by a change in pH from 8.6 to 7.6. By contrast, olfactory capacity was partially restored by increasing dissolved organic carbon (DOC; 0.1-6.0 mg/L). Given the range of natural water quality conditions in the western United States, water hardness and alkalinity are unlikelyto protect threatened or endangered salmon from the sensory neurotoxicity of copper. However, the olfactory toxicity of copper may be partially reduced in surface waters that have a high DOC content.

  10. Microbiology of broiler carcasses and chemistry of chiller water as affected by water reuse.

    Science.gov (United States)

    Northcutt, J K; Smith, D; Huezo, R I; Ingram, K D

    2008-07-01

    A study was conducted to determine the effects of treating and reusing poultry chiller water in a commercial poultry processing facility. Broiler carcasses and chiller water were obtained from a commercial processing facility which had recently installed a TOMCO Pathogen Management System to recycle water in sections 2 and 3 of two 3-compartment chillers. In this system, reused water is blended with fresh water to maintain the chiller volume. Carcasses were sampled prechill and postchill (final exit), and chiller water was sampled from the beginning and end of each of the 3 sections. Carcasses were subjected to a whole carcass rinse (WCR) in 0.1% peptone. Numbers of Escherichia coli (EC), coliforms (CF), and Campylobacter (CPY) were determined from the WCR and chiller water samples. Prevalence of Salmonella (SAL) was also determined on the WCR and chiller water samples. On average, prechill levels of bacteria recovered from rinses were 2.6, 2.9, and 2.6 log10 cfu/mL for EC, CF, and CPY, respectively. Ten out of 40 (25%) prechill carcasses were positive for SAL. After chilling, numbers of EC, CF, and CPY recovered from carcass rinses decreased by 1.5, 1.5, and 2.0 log10 cfu/mL, respectively. However, 9 out of 40 (22%) postchill carcasses were positive for SAL. When the chiller water samples were tested, counts of EC, CF, and CPY were found only in water collected from the first section of the chiller (inlet and outlet). Two of 4 water samples collected from the inlet of the first section tested positive for SAL. This study shows that fresh and reused water can be used to cool poultry in chiller systems to achieve a reduction in numbers of bacteria (EC, CF, and CPY) or equivalent prevalence (SAL) of bacteria recovered from broiler carcasses.

  11. Water as Life, Death, and Power: Building an Integrated Interdisciplinary Course Combining Perspectives from Anthropology, Biology, and Chemistry

    Science.gov (United States)

    Willermet, Cathy; Mueller, Anja; Juris, Stephen J.; Drake, Eron; Upadhaya, Samik; Chhetri, Pratik

    2013-01-01

    In response to a request from a campus student organization, faculty from three fields came together to develop and teach an integrated interdisciplinary course on water issues and social activism. This course, "Water as Life, Death, and Power", brought together topics from the fields of anthropology, biology and chemistry to explore…

  12. Hydrogeologic controls of surface-water chemistry in the Adirondack region of New York State

    Science.gov (United States)

    Peters, N.E.; Driscoll, C.T.

    1987-01-01

    Relationships between surface-water discharge, water chemistry, and watershed geology were investigated to evaluate factors affecting the sensitivity of drainage waters in the Adirondack region of New York to acidification by atmospheric deposition. Instantaneous discharge per unit area was derived from relationships between flow and staff-gage readings at 10 drainage basins throughout the region. The average chemical composition of the waters was assessed from monthly samples collected from July 1982 through July 1984. The ratio of flow at the 50-percent exceedence level to the flow at the 95-percent exceedence level of flow duration was negatively correlated with mean values of alkalinity or acid-neutralizing capacity (ANC), sum of basic cations (SBC), and dissolved silica, for basins containing predominantly aluminosilicate minerals and little or no carbonate-bearing minerals. Low ratios are indicative of systems in which flow is predominately derived from surface- and ground-water storage, whereas high ratios are characteristic of watersheds with variable flow that is largely derived from surface runoff. In an evaluation of two representative surface-water sites, concentrations of ANC, SBC, and dissolved silica, derived primarily from soil mineral weathering reactions. decreased with increasing flow. Furthermore, the ANC was highest at low flow when the percentage of streamflow derived from ground water was maximum. As flow increased, the ANC decreased because the contribution of dilute surface runoff and lateral flow through the shallow acidic soil horizons to total flow increased. Basins having relatively high ground-water contributions to total flow, in general, have large deposits of thick till or stratified drift. A major factor controlling the sensitivity of these streams and lakes to acidification is the relative contribution of ground water to total discharge. ?? 1987 Martinus Nijhoff/Dr W. Junk Publishers.

  13. Modeling water chemistry change and contaminant transport in riverbank filtration systems

    Science.gov (United States)

    Mustafa, Shaymaa; Bahar, Arifah; Aziz, Zainal Abdul; Suratman, Saim

    2016-06-01

    Riverbank filtration system is river water treatment approach based on natural removal of contaminants due to physical, chemical and biological processes. In this article, an analytical model is developed by using Green's function method to simulate the effects of pumping well and microbial activity that occurs in riverbed sediments on contaminant transport and evolution of water chemistry. The model is tested with data collected previously for RBF site in France. The results are compared with numerical simulation conducted in the literature by using finite difference method. Graphically, it is noticed that both numerical and analytical results have almost the same behavior. Also it is found that the model can simulate the decreasing of one pollutant concentration at the zone where the bacteria starts to consume this pollutant.

  14. Trends in the chemistry of atmospheric deposition and surface waters in the Lake Maggiore catchment

    Directory of Open Access Journals (Sweden)

    M. Rogora

    2001-01-01

    Full Text Available The Lake Maggiore catchment is the area of Italy most affected by acid deposition. Trend analysis was performed on long-term (15-30 years series of chemical analyses of atmospheric deposition, four small rivers draining forested catchments and four high mountain lakes. An improvement in the quality of atmospheric deposition was detected, due to decreasing sulphate concentration and increasing pH. Similar trends were also found in high mountain lakes and in small rivers. Atmospheric deposition, however, is still providing a large and steady flux of nitrogen compounds (nitrate and ammonium which is causing increasing nitrogen saturation in forest ecosystems and increasing nitrate levels in rivers. Besides atmospheric deposition, an important factor controlling water acidification and recovery is the weathering of rocks and soils which may be influenced by climate warming. A further factor is the episodic deposition of Saharan calcareous dust which contributes significantly to base cation deposition. Keywords: trend, atmospheric deposition, nitrogen, stream water chemistry.

  15. Water chemistry in heat and cold supply (district heating/cooling)

    Energy Technology Data Exchange (ETDEWEB)

    Deelen-Bremer, Marga van; Vos, Frank de; Heijboer, Rob [KEMA Nederland B.V. (Netherlands)

    2010-07-01

    District heating is seen as an important pillar in the CO{sub 2} reduction. Since the Kyoto protocol with the target for reduction of greenhouse gases, a renewed interest in district heating is visible. District heating and increasingly district cooling can be used for heating/cooling of houses, but also for large buildings and greenhouses. Combined heat and power (CHP), waste incinerator, but also rest heat of industry can provide the heat for district heating. On the other hand cold surface water, groundwater, but also rest heat can be used for district cooling. With the growing heat/cold supply market, also an even larger growth in cases of damages in district heating systems is wittnessed. Damages were chemistry can play an preventing role. A good conditioning of the district heating water, combined with proper monitoring, will safeguard the integrity of the system. (orig.)

  16. Physical chemistry of water droplets in wafer cleaning with low water use

    NARCIS (Netherlands)

    Donck, J.C.J. van der; Bakker, J.; Smeltink, J.A.; Kolderweij, R.B.J.; Zon, B.C.M.B. van der; Kleef, M.H. van

    2015-01-01

    Reduction of water and energy consumption is of importance for keeping viable industry in Europe. In 2012 the Eniac project Silver was started in order to reduce water and energy consumption in the semiconductor industry by 10% [1]. Cleaning of wafers is one of the key process steps that require a h

  17. On the interaction between fuel crud and water chemistry in nuclear power plants

    Energy Technology Data Exchange (ETDEWEB)

    Jiaxin Chen [Studsvik Material AB, Nykoeping (Sweden)

    2000-01-01

    This report has surveyed the current understanding about the characteristics of fuel crud, its deposition and dissolution behaviour, the influences of water chemistry, and the radioactivity transport in nuclear power plants. The references were mainly sought for from the International Nuclear Information System (INIS) database and some internal reports of Studsvik Material AB. The characteristics of fuel crud from discharged fuel rods have been extensively investigated over the last three decades. Fuel crud mainly consists of iron, nickel and chromium oxides. For BWR fuel crud the main phases are hematite and nonstoichiometric nickel ferrite spinels. For PWR fuel crud the main phases are nonstoichiometric nickel ferrite and nickel metal or nickel oxide. Fuel crud is usually thin and relatively porous in the outer layer but dense in the inner layer. Important information is lacking about the adhesion property of crud particles or agglomerates on fuel rods. Little, if any, information is reported about the characteristics of fuel crud before discharging in pool. It is uncertain if the fuel crud can, after pool discharge, largely preserve its characteristics appearing during reactor operation. Deposition behaviour of corrosion products on fuel rods, in both solid particles and ionic forms in reactor water, has been well studied in the simulated reactor water environments without irradiation. The influences on deposition rate of pH, heat flux, particle size, crud concentration, and flow rate have also been studied in detail. Most of the experimental observations may be qualitatively explained by the theories developed. However, the importance of each influencing parameter remains largely unknown in the complicated reactor water environments, because irradiation, among various influencing factors, may play an important role. The behaviour of crud dissolution has been extensively studied in various reactor water environments. Generally speaking, the more easily crud

  18. Anthropogenic impact on water chemistry and benthic macroinvertebrate associated changes in a southern Nigeria stream.

    Science.gov (United States)

    Arimoro, Francis O; Odume, O Nelson; Uhunoma, Samson I; Edegbene, Augustine O

    2015-02-01

    The Ogba River in southern Nigeria is an important water resource for its riparian communities. This study evaluates impact of anthropogenic influences on the Ogba River using water chemistry and macroinvertebrate data sets obtained over a period of 6 months between January and June 2012. Four stations, stations 1-4, characterised by various human activities were chosen along the river. Organic wastes from domestic and industrial sources were the major point sources of pollutants. Station 2 where the municipal wastewater drains into the river had elevated values of flow velocity, BOD5, sulphate, phosphate, nitrate and sodium. Based on the canonical correspondence analysis (CCA), 5-day biochemical oxygen demand (BOD5), sulphate, nitrate and phosphate were the main factors that help to shape the macroinvertebrate assemblage structure of the Ogba River. Macroinvertebrates clustered strongly by stations than by seasons indicating that water quality differences between the stations were responsible for the observed differences in the biotic assemblage. The preponderance of naidid oligochaetes, baetid nymphs and certain tolerant dipteran taxa including chironomids and ceratopogonids at all four stations was an indication that the entire water body was stressed. The odonates were the single most abundant taxa; their dominance could be attributed to the vegetative nature of the stream, favouring odonate colonisation. Overall, the responses of macroinvertebrates to stress were reflected by the different assemblage structures recorded at the four study stations. Substrate and microhabitat obliteration and poor water quality appeared to be the factors responsible for the observed assemblage structure in the Ogba River.

  19. Impact of Water Chemistry, Pipe Material and Stagnation on the Building Plumbing Microbiome.

    Directory of Open Access Journals (Sweden)

    Pan Ji

    Full Text Available A unique microbiome establishes in the portion of the potable water distribution system within homes and other buildings (i.e., building plumbing. To examine its composition and the factors that shape it, standardized cold water plumbing rigs were deployed at the treatment plant and in the distribution system of five water utilities across the U.S. Three pipe materials (copper with lead solder, CPVC with brass fittings or copper/lead combined pipe were compared, with 8 hour flush cycles of 10 minutes to simulate typical daily use patterns. High throughput Illumina sequencing of 16S rRNA gene amplicons was employed to profile and compare the resident bulk water bacteria and archaea. The utility, location of the pipe rig, pipe material and stagnation all had a significant influence on the plumbing microbiome composition, but the utility source water and treatment practices were dominant factors. Examination of 21 water chemistry parameters suggested that the total chlorine concentration, pH, P, SO42- and Mg were associated with the most of the variation in bulk water microbiome composition. Disinfectant type exerted a notably low-magnitude impact on microbiome composition. At two utilities using the same source water, slight differences in treatment approaches were associated with differences in rare taxa in samples. For genera containing opportunistic pathogens, Utility C samples (highest pH of 9-10 had the highest frequency of detection for Legionella spp. and lowest relative abundance of Mycobacterium spp. Data were examined across utilities to identify a true universal core, special core, and peripheral organisms to deepen insight into the physical and chemical factors that shape the building plumbing microbiome.

  20. Remote assessment of instantaneous changes in water chemistry after liming in a Nova Scotia catchment

    Science.gov (United States)

    Angelidis, Christine

    2013-04-01

    Remote assessment of instantaneous changes in water chemistry after liming in a Nova Scotia catchment ANGELIDIS, C.1, STERLING, S.1, BREEN, A.2, BIAGI, K.1., and CLAIR, T.A.1 1Dalhousie University, christine.angelidis@dal.ca, 2Bluenose Coastal Action Foundation, andrew@coastalaction.org Southwestern Nova Scotia has some of the most acidic freshwaters in North America due to its location downwind of the major emission sources in eastern Canada and the US and due to a resistant geology which offers little acid buffering capacity (Clair et al. 2007). Because of the poor buffering and regionally high runoff values, hydrological events such as snowmelt and rain storms are frequent and can cause sudden changes in water chemistry which can have devastating effects on freshwater biota due to increases in acidity and metals (Dennis and Clair in press). Clair et al. (2001) have estimated the potential frequency of acidic episodes in this region based on a number of hydrological factors, though the technology available at the time to monitor short-term changes was not dependable. Recent advances in equipment have made the assessment of the frequency and severity of acidic episodes easier and more accurate, allowing better interpretation and prediction of hydrogeochemical changes with variations in weather and deposition patterns. Here we take advantage of these recent advances to monitor water chemistry in an experimental catchment, and explore the response to catchment liming. Catchment liming is one way of mitigating the effects of acid deposition in sensitive areas. We limed a 50 ha catchment at a rate of 5 t/ha in the Gold River watershed of southwest Nova Scotia to examine the interactions between application of lime with the geological and climatological conditions of this region and acid episode frequency. In order to assess changes of episode frequency caused by liming, we established two mobile environmental monitoring platforms in the catchment: a control site

  1. H02 WETLAND TREATMENT SYSTEM WATER CHEMISTRY SAMPLING AND RESULTS REPORT

    Energy Technology Data Exchange (ETDEWEB)

    Bach, M; Michael Serrato, M; Eric Nelson, E

    2008-02-15

    The H-02 Wetland Treatment System (Figure 1) is used to remove heavy metals (e.g., copper and zinc) from the H-Area process and storm water discharge. Routine flow enters an equalization basin by inlets on either the east (Location 1) or west end (Location 2). The west end influent constitutes 75% of the average flow into the basin which has an average residence time of approximately 3 days at low pool (i.e., 120 gal/min. through a volume of 0.5 million gallons). The water then exits via the basin outlet on the east end. Next, the water flows to a splitter box (Location 3) which evenly separates the flow between two wetland cells for a design flow of 60 gal/min. per wetland cell with a residence time in the cell of approximately 2 days. The wetland effluent is then combined (Location 4) and flows through a spillway before reaching the National Pollution Discharge Elimination System (NPDES) measurement point near Road 4. During initial operation, it was observed that the pH of the water leaving the equalization basin was elevated compared to the influent pH. Furthermore, the elevated pH remained through the wetland cells so that there was an average pH of 10 leaving the wetland cells during the daytime which exceeds the upper NPDES limit of 8.5. The purpose of the current study was to evaluate the cause of the increase in pH within the equalization basin of the H-02 Wetland Treatment System. Possible mechanisms included algal activity and inorganic chemistry interactions (e.g., interactions with the clay and/or bentonite liner). Water quality parameters were evaluated throughout the H-02 Wetland Treatment system and over time in order to determine the cause of high pH values measured in the basin and wetland. Fluctuations in dissolved oxygen (DO) and accompanying changes in pH would be expected in systems where algae are an influencing factor. An unexpected increase or decrease in the concentration of inorganic substances may indicate operational changes or an

  2. Oxide/Water Interfaces: How the Surface Chemistry Modifies the Electronic Energy Alignment

    Science.gov (United States)

    Sprik, Michiel

    2014-03-01

    The minimum of the d-electron conduction band of an aqueous transition metal oxide electrode is typically no more than a few 100 mV away from the standard hydrogen electrode (SHE). Because of this favourable alignment of the electronic energy levels (near) metallic transition metal oxides with partly filled d bands can be used as electrocatalysts while the compounds with finite electronic gap can be used as photocatalysts. However, because of their ionic character, transition metal-oxide surfaces also show amphiphilic acid-base activity. At low pH the basic sites are protonated and at high pH the acidic sites deprotonated creating an electrical double layer with corresponding surface potential. The alignment of the electronic energy levels, and by implication their redox activity, is therefore pH dependent. In fact, even in absence of protonic surface charge, the coordination with water molecules is already capable of shifting the electronic energy levels of the oxide by 1 eV or more. Computation of the electronic energies in transition metal oxide electrodes requires therefore a detailed modeling of their aqueous surface chemistry. The solvation energy of the proton is the common energy reference for both redox potentials on the SHE scale and acidity constants (pKa). Computation of the H+ solvation energy is therefore a key component in a unified treatment of redox and acid-base chemistry. In this talk we outline the Density Functional Theory based Molecular Dynamics (DFTMD) method we have developed for this purpose. The central tool of our approach is a method for reversible insertion of protons in the aqueous part of the DFTMD model system. As an illustration we discuss the application to the rutile TiO2/water and MnO2/water interface.

  3. Fracture control of ground water flow and water chemistry in a rock aquitard.

    Science.gov (United States)

    Eaton, Timothy T; Anderson, Mary P; Bradbury, Kenneth R

    2007-01-01

    There are few studies on the hydrogeology of sedimentary rock aquitards although they are important controls in regional ground water flow systems. We formulate and test a three-dimensional (3D) conceptual model of ground water flow and hydrochemistry in a fractured sedimentary rock aquitard to show that flow dynamics within the aquitard are more complex than previously believed. Similar conceptual models, based on regional observations and recently emerging principles of mechanical stratigraphy in heterogeneous sedimentary rocks, have previously been applied only to aquifers, but we show that they are potentially applicable to aquitards. The major elements of this conceptual model, which is based on detailed information from two sites in the Maquoketa Formation in southeastern Wisconsin, include orders of magnitude contrast between hydraulic diffusivity (K/S(s)) of fractured zones and relatively intact aquitard rock matrix, laterally extensive bedding-plane fracture zones extending over distances of over 10 km, very low vertical hydraulic conductivity of thick shale-rich intervals of the aquitard, and a vertical hydraulic head profile controlled by a lateral boundary at the aquitard subcrop, where numerous surface water bodies dominate the shallow aquifer system. Results from a 3D numerical flow model based on this conceptual model are consistent with field observations, which did not fit the typical conceptual model of strictly vertical flow through an aquitard. The 3D flow through an aquitard has implications for predicting ground water flow and for planning and protecting water supplies.

  4. Mineralogical Diversity in Lake Pavin: Connections with Water Column Chemistry and Biomineralization Processes

    Directory of Open Access Journals (Sweden)

    Jennyfer Miot

    2016-03-01

    Full Text Available As biominerals are good tracers of microbial interactions with the environment, they may provide signatures of microbial evolution and paleoenvironmental conditions. Since modern analogues of past environments help with defining proxies and biosignatures, we explored microbe mineral interactions in the water column of a maar lake, located in France: Lake Pavin. This lake is considered as a potential Precambrian ocean analogue, as it is ferruginous and meromictic, i.e., stratified with a superficial O2-rich layer (mixolimnion and a deeper permanently anoxic layer (monimolimnion. We combined bulk chemical analyses of dissolved and particulate matter in combination with electron microscopy analyses of the particulate matter at different depths along the water column. The mineralogy changed along with water chemistry, and most of the minerals were intimately associated with microorganisms. Evolution of the redox conditions with depth leads to the successive precipitation of silica and carbonates, Mn-bearing, Fe-bearing and S-containing phases, with a predominance of phosphates in the monimolimnion. This scheme parallels the currently-assessed changes of microbial diversity with depth. The present results corroborate previous studies that suggested a strong influence of microbial activity on mineralogical diversity through extracellular and intracellular biomineralization. This paper reports detailed data on mineralogical profiles of the water column and encourages extended investigation of these processes.

  5. Lake Bolsena (Central Italy: an updating study on its water chemistry

    Directory of Open Access Journals (Sweden)

    Piero BRUNI

    2004-02-01

    Full Text Available In spite of its importance as regards size (volume 9.2 106 m3, max depth 151 m and as a source of drinking water, Lake Bolsena has not been studied from a hydrochemical point of view since the second half of the 60s, when a group of researchers from the Istituto Italiano di Idrobiologia co-ordinated a complete study of the limnology of the Latium lakes Bolsena, Albano, Vico, and Bracciano. In the following years analyses were performed sporadically; since the 90s, temperature and oxygen profiles and other studies were made by the Associazione Lago di Bolsena. Based on chemical profiles made in 2001-2003, this paper discusses the present chemical composition of Lake Bolsena waters, and compares them with those of other volcanic lakes in Latium (Bracciano, Albano, Nemi and Vico. The paper briefly considers the main factors influencing the water chemistry of Lake Bolsena, the variations observed from the analyses of the 60s, and the main sources of risk to water quality.

  6. Wettability and surface chemistry of crystalline and amorphous forms of a poorly water soluble drug.

    Science.gov (United States)

    Puri, Vibha; Dantuluri, Ajay K; Kumar, Mahesh; Karar, N; Bansal, Arvind K

    2010-05-12

    The present study compares energetics of wetting behavior of crystalline and amorphous forms of a poorly water soluble drug, celecoxib (CLB) and attempts to correlate it to their surface molecular environment. Wettability and surface free energy were determined using sessile drop contact angle technique and water vapor sorption energetics was measured by adsorption calorimetry. The surface chemistry was elucidated by X-ray photoelectron spectroscopy (XPS) and crystallographic evaluation. The two solid forms displayed distinctly different wetting with various probe liquids and in vitro dissolution media. The crystalline form surface primarily exhibited dispersive surface energy (47.3mJ/m(2)), while the amorphous form had a slightly reduced dispersive (45.2mJ/m(2)) and a small additional polar (4.8mJ/m(2)) surface energy. Calorimetric measurements, revealed the amorphous form to possess a noticeably high differential heat of absorption, suggesting hydrogen bond interactions between its polar energetic sites and water molecules. Conversely, the crystalline CLB form was found to be inert to water vapor sorption. The relatively higher surface polarity of the amorphous form could be linked to its greater oxygen-to-fluorine surface concentration ratio of 1.27 (cf. 0.62 for crystalline CLB), as determined by XPS. The crystallographic studies of the preferred cleavage plane (020) of crystalline CLB further supported its higher hydrophobicity. In conclusion, the crystalline and amorphous forms of CLB exhibited disparate surface milieu, which in turn can have implications on the surface mediated events.

  7. Investigation of adsorption of surfactant at the air-water interface with quantum chemistry method

    Institute of Scientific and Technical Information of China (English)

    CHEN MeiLing; WANG ZhengWu; WANG HaiJun; ZHANG GeXin; TAO FuMing

    2007-01-01

    Density functional theory (DFT) of quantum chemistry was used to optimize the configuration of the anionic surfactant complexes CH3(CH2)7OSO-3(H2O)n (n=0-6) and calculate their molecular frequencies at the B3LYP/6-311+G* level. The interaction of CH3(CH2)7OSO-3 with 1 to 6 water molecules was investigated at the air-water interface with DFT. The results revealed that the hydration shell was formed in the form of H-bond between the hydrophilic group of CH3(CH2)7OSO-3 and 6 waters. The strength of H-bonds belongs to medium. Binding free energy revealed that the hydration shell was stable. The increase of the number of water molecules will cause increases of the total charge of hydrophilic group and S10-O9-C8 bond angle, but decreases of the alkyl chain length and the bond lengths of S10-O11,S10-O12 as well as S10-O13, respectively.

  8. A pinch of salt is all it takes: chemistry at the frozen water surface.

    Science.gov (United States)

    Kahan, Tara F; Wren, Sumi N; Donaldson, D James

    2014-05-20

    Chemical interactions at the air-ice interface are of great importance to local atmospheric chemistry but also to the concentrations of pollutants deposited onto natural snow and ice. However, the study of such processes has been hampered by the lack of general, surface-specific probes. Even seemingly basic chemical properties, such as the local concentration of chemical compounds, or the pH at the interface, have required the application of assumptions about solute distributions in frozen media. The measurements that have been reported have tended for the most part to focus on entire ice or snow samples, rather than strictly the frozen interface with the atmosphere. We have used glancing-angle laser spectroscopy to interrogate the air-ice interface; this has yielded several insights into the chemical interactions there. The linear fluorescence and Raman spectra thus measured have the advantage of easy interpretability; careful experimentation can limit their probe depth to that which is relevant to atmospheric heterogeneous processes. We have used these techniques to show that the environment at the interface between air and freshwater ice surfaces is distinct from that at the interface between air and liquid water. Acids such as HCl that adsorb to ice surfaces from the gas phase result in significantly different pH responses than those at liquid water surfaces. Further, the solvation of aromatic species is suppressed at freshwater ice surfaces compared with that at liquid water surfaces, leading to extensive self-association of aromatics at ice surfaces. Photolysis kinetics of these species are much faster than at liquid water surfaces; this can sometimes (but not always) be explained by red shifts in the absorption spectra of self-associated aromatics increasing the extent to which solar radiation is absorbed. The environment presented by frozen saltwater surfaces, in contrast, appears to be reasonably well-described by liquid water. The extent of hydrogen

  9. Water Chemistry Control System for Recovery of Damaged and Degraded Spent Fuel

    Energy Technology Data Exchange (ETDEWEB)

    Sindelar, R.; Fisher, D.; Thomas, J.

    2011-02-18

    The International Atomic Energy Agency (IAEA) and the government of Serbia have led the project cosponsored by the U.S, Russia, European Commission, and others to repackage and repatriate approximately 8000 spent fuel elements from the RA reactor fuel storage basins at the VIN?A Institute of Nuclear Sciences to Russia for reprocessing. The repackaging and transportation activities were implemented by a Russian consortium which includes the Sosny Company, Tekhsnabeksport (TENEX) and Mayak Production Association. High activity of the water of the fuel storage basin posed serious risk and challenges to the fuel removal from storage containers and repackaging for transportation. The risk centered on personnel exposure, even above the basin water, due to the high water activity levels caused by Cs-137 leached from fuel elements with failed cladding. A team of engineers from the U.S. DOE-NNSA's Global Threat Reduction Initiative, the Vinca Institute, and the IAEA performed the design, development, and deployment of a compact underwater water chemistry control system (WCCS) to remove the Cs-137 from the basin water and enable personnel safety above the basin water for repackaging operations. Key elements of the WCCS system included filters, multiple columns containing an inorganic sorbent, submersible pumps and flow meters. All system components were designed to be remotely serviceable and replaceable. The system was assembled and successfully deployed at the Vinca basin to support the fuel removal and repackaging activities. Following the successful operations, the Cs-137 is now safely contained and consolidated on the zeolite sorbent used in the columns of the WCCS, and the fuel has been removed from the basins. This paper reviews the functional requirements, design, and deployment of the WCCS.

  10. Effect of water chemistry upsets on the dynamics of corrective reagent dosing systems at thermal power stations

    Science.gov (United States)

    Voronov, V. N.; Yegoshina, O. V.; Bolshakova, N. A.; Yarovoi, V. O.; Latt, Aie Min

    2016-12-01

    Typical disturbances in the dynamics of a corrective reagent dosing system under unsteady-state conditions during the unsatisfactory operation of a chemical control system with some water chemistry upsets at thermal and nuclear power stations are considered. An experimental setup representing a physical model for the water chemistry control system is described. The two disturbances, which are most frequently encountered in water chemistry control practice, such as a breakdown or shutdown of temperature compensation during pH measurement and an increase in the heat-transfer fluid flow rate, have been modeled in the process of study. The study of the effect produced by the response characteristics of chemical control analyzers on the operation of a reagent dosing system under unsteady-state conditions is important for the operative control of a water chemistry regime state. The effect of temperature compensation during pH measurement on the dynamics of an ammonia-dosing system in the manual and automatic cycle chemistry control modes has been studied. It has been demonstrated that the reading settling time of a pH meter in the manual ammonia- dosing mode grows with a breakdown in temperature compensation and a simultaneous increase in the temperature of a heat-transfer fluid sample. To improve the efficiency of water chemistry control, some systems for the quality control of a heat-transfer fluid by a chemical parameter with the obligatory compensation of a disturbance in its flow rate have been proposed for use. Experimental results will possibly differ from industrial data due to a great length of sampling lines. For this reason, corrective reagent dosing systems must be adapted to the conditions of a certain power-generating unit in the process of their implementation.

  11. Microbial metabolism alters pore water chemistry and increases consolidation of oil sands tailings.

    Science.gov (United States)

    Arkell, Nicholas; Kuznetsov, Petr; Kuznetsova, Alsu; Foght, Julia M; Siddique, Tariq

    2015-01-01

    Tailings produced during bitumen extraction from surface-mined oil sands ores (tar sands) comprise an aqueous suspension of clay particles that remain dispersed for decades in tailings ponds. Slow consolidation of the clays hinders water recovery for reuse and retards volume reduction, thereby increasing the environmental footprint of tailings ponds. We investigated mechanisms of tailings consolidation and revealed that indigenous anaerobic microorganisms altered porewater chemistry by producing CO and CH during metabolism of acetate added as a labile carbon amendment. Entrapped biogenic CO decreased tailings pH, thereby increasing calcium (Ca) and magnesium (Mg) cations and bicarbonate (HCO) concentrations in the porewater through dissolution of carbonate minerals. Soluble ions increased the porewater ionic strength, which, with higher exchangeable Ca and Mg, decreased the diffuse double layer of clays and increased consolidation of tailings compared with unamended tailings in which little microbial activity was observed. These results are relevant to effective tailings pond management strategies.

  12. Effects on water chemistry, benthic invertebrates and brown trout following forest fertilization in central Sweden

    Energy Technology Data Exchange (ETDEWEB)

    Goethe, L.; Soederberg, H.; Sjoelander, E. (County Administrative Board of Vaesternorrland, Haernoesand (Sweden). Environmental Unit); Nohrstedt, H.Oe. (Inst. for Forest Improvement, Uppsala (Sweden))

    1993-01-01

    Two coniferous forest drainage areas in central Sweden were partially fertilized with ammonium nitrate and calcium ammonium nitrate respectively, both at a dose of 150 kg N per ha. During the following years observations were made on stream water chemistry, invertebrates and brown trout (Salmo trutta L.). Upstream stations were used as controls. Very high concentrations of inorganic N (up to 45 mg l[sup -1]) were recorded immediately after the fertilization. Thereafter, concentration decreased rapidly but remained elevated during the whole study period. Acidity conditions (pH, alkalinity, aluminium) were unaffected by both treatments. The only registered effect on the benthic fauna was a three- to five-fold increase of drifting invertebrates during the first four-five days after the treatment. However, this did not reduce the population density at the treated stations. No effects on population of trout were recorded. (22 refs., 6 figs., 3 tabs.).

  13. Stream Water and Soil Water Chemistry Following the Table Mountain Wildfire, Washington

    Science.gov (United States)

    Roccanova, V. J.; Gazis, C. A.

    2013-12-01

    Severe wildfire occurrence in the Western United States increased throughout the 20th century and has continued to increase into the 21st century. Global climate change resulting from natural and anthropogenic sources is considered a contributor to this increase in wildfire severity. Fire suppression techniques developed in the early 20th century are also a factor in increased severe wildfire occurrence as they augment available fuel loads. Biomass burning releases nutrients that are held within trees and plants. Nitrogen, phosphorous, and calcium levels have been documented as increasing in stream waters as a result of wildfire. As severe wildfire occurrence increases, so does the likelihood that stream, and to a lesser extent groundwater, will be loaded with nutrients and sediments as a result of wildfire activity. Increased nutrient loads can cause algal blooms that deplete streams of oxygen, important to aquatic plants and animals that reside in these streams. These changes in water quality can also affect humans who depend on these streams for irrigation and drinking water purposes. The Table Mountain wildfire in Washington State was started by a lightning strike that occurred at approximately 8:00 PM on Saturday September 8th, 2012. The fire burned for approximately one month and was declared to be 100% contained on Friday October 5th, 2012. Over this period the fire burned a total of 171 square kilometers of forest. In this study multiple stream and soil water samples were collected from three types of area in the winter through summer following the fire: severely burned, moderately burned, and unburned. All areas sampled have similar bedrock and vegetation cover. These samples were analyzed for major ions and trace element concentrations. Select samples will also be analyzed for strontium isotope ratios. The results of these geochemical analyses will be presented. Because calcium and strontium have similar properties, their concentrations can be combined

  14. Supramolecular organic frameworks: engineering periodicity in water through host-guest chemistry.

    Science.gov (United States)

    Tian, Jia; Chen, Lan; Zhang, Dan-Wei; Liu, Yi; Li, Zhan-Ting

    2016-05-11

    The development of homogeneous, water-soluble periodic self-assembled structures comprise repeating units that produce porosity in two-dimensional (2D) or three-dimensional (3D) spaces has become a topic of growing interest in the field of supramolecular chemistry. Such novel self-assembled entities, known as supramolecular organic frameworks (SOFs), are the result of programmed host-guest interactions, which allows for the thermodynamically controlled generation of monolayer sheets or a diamondoid architecture with regular internal cavities or pores under mild conditions. This feature article aims at propagating the conceptually novel SOFs as a new entry into conventional supramolecular polymers. In the first section, we will describe the background of porous solid frameworks and supramolecular polymers. We then introduce the self-assembling behaviour of several multitopic flexible molecules, which is closely related to the design of periodic SOFs from rigid multitopic building blocks. This is followed by a brief discussion of cucurbit[8]uril (CB[8])-encapsulation-enhanced aromatic stacking in water. The three-component host-guest pattern based on this stacking motif has been utilized to drive the formation of most of the new SOFs. In the following two sections, we will highlight the main advances in the construction of 2D and 3D SOFs and the related functional aspects. Finally, we will offer our opinions on future directions for both structures and functions. We hope that this article will trigger the interest of researchers in the field of chemistry, physics, biology and materials science, which should help accelerate the applications of this new family of soft self-assembled organic frameworks.

  15. Vertical Gradients in Water Chemistry and Age in the Southern High Plains Aquifer, Texas, 2002

    Science.gov (United States)

    McMahon, P.B.; Böhlke, J.K.; Lehman, T.M.

    2004-01-01

    The southern High Plains aquifer is the primary source of water used for domestic, industrial, and irrigation purposes in parts of New Mexico and Texas. Despite the aquifer's importance to the overall economy of the southern High Plains, fundamental ground-water characteristics, such as vertical gradients in water chemistry and age, remain poorly defined. As part of the U.S. Geological Survey's National Water-Quality Assessment Program, water samples from nested, short-screen monitoring wells installed in the southern High Plains aquifer at two locations (Castro and Hale Counties, Texas) were analyzed for field parameters, major ions, nutrients, trace elements, dissolved organic carbon, pesticides, stable and radioactive isotopes, and dissolved gases to evaluate vertical gradients in water chemistry and age in the aquifer. Tritium measurements indicate that recent (post-1953) recharge was present near the water table and that deeper water was recharged before 1953. Concentrations of dissolved oxygen were largest (2.6 to 5.6 milligrams per liter) at the water table and decreased with depth below the water table. The smallest concentrations were less than 0.5 milligram per liter. The largest major-ion concentrations generally were detected at the water table because of the effects of overlying agricultural activities, as indicated by postbomb tritium concentrations and elevated nitrate and pesticide concentrations at the water table. Below the zone of agricultural influence, major-ion concentrations exhibited small increases with depth and distance along flow paths because of rock/water interactions and mixing with water from the underlying aquifer in rocks of Cretaceous age. The concentration increases primarily were accounted for by dissolved sodium, bicarbonate, chloride, and sulfate. Nitrite plus nitrate concentrations at the water table were 2.0 to 6.1 milligrams per liter as nitrogen, and concentrations substantially decreased with depth in the aquifer to a

  16. Multivariate Statistical Analysis of Water Chemistry in Evaluating the Origin of Contamination in Many Devils Wash, Shiprock, New Mexico

    Energy Technology Data Exchange (ETDEWEB)

    None, None

    2012-12-31

    This report evaluates the chemistry of seep water occurring in three desert drainages near Shiprock, New Mexico: Many Devils Wash, Salt Creek Wash, and Eagle Nest Arroyo. Through the use of geochemical plotting tools and multivariate statistical analysis techniques, analytical results of samples collected from the three drainages are compared with the groundwater chemistry at a former uranium mill in the Shiprock area (the Shiprock site), managed by the U.S. Department of Energy Office of Legacy Management. The objective of this study was to determine, based on the water chemistry of the samples, if statistically significant patterns or groupings are apparent between the sample populations and, if so, whether there are any reasonable explanations for those groupings.

  17. Plasma Discharges in Gas Bubbles in Liquid Water: Breakdown Mechanisms and Resultant Chemistry

    Science.gov (United States)

    Gucker, Sarah M. N.

    The use of atmospheric pressure plasmas in gases and liquids for purification of liquids has been investigated by numerous researchers, and is highly attractive due to their strong potential as a disinfectant and sterilizer. However, the fundamental understanding of plasma production in liquid water is still limited. Despite the decades of study dedicated to electrical discharges in liquids, many physical aspects of liquids, such as the high inhomogeneity of liquids, complicate analyses. For example, the complex nonlinearities of the fluid have intricate effects on the electric field of the propagating streamer. Additionally, the liquid material itself can vaporize, leading to discontinuous liquid-vapor boundaries. Both can and do often lead to notable hydrodynamic effects. The chemistry of these high voltage discharges on liquid media can have circular effects, with the produced species having influence on future discharges. Two notable examples include an increase in liquid conductivity via charged species production, which affects the discharge. A second, more complicated scenario seen in some liquids (such as water) is the doubling or tripling of molecular density for a few molecule layers around a high voltage electrode. These complexities require technological advancements in optical diagnostics that have only recently come into being. This dissertation investigates several aspects of electrical discharges in gas bubbles in liquids. Two primary experimental configurations are investigated: the first allows for single bubble analysis through the use of an acoustic trap. Electrodes may be brought in around the bubble to allow for plasma formation without physically touching the bubble. The second experiment investigates the resulting liquid phase chemistry that is driven by the discharge. This is done through a dielectric barrier discharge with a central high voltage surrounded by a quartz discharge tube with a coil ground electrode on the outside. The plasma

  18. Water chemistry in Kuji river. Its spatial and seasonal variations in major ions and organic substances

    Energy Technology Data Exchange (ETDEWEB)

    Niina, Toshiaki; Matsunaga, Takeshi; Amano, Hikaru [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    1996-02-01

    As a basic research with a aim to clarify the migration behavior of radionuclides in rivers, the characteristics of dissolved ions and organic substances in river water, which characteristics may affect the behavior, was investigated. The investigation was carried out for the Kuji river in the northern Kanto district (Japan) comprising four sampling campaigns in 1994 for 10 locations from the upstream to the downstream. Concentrations of major ions, iron and manganese species and organic substances were analyzed in laboratory. Values of temperature of the water, pH, conductivity, dissolved oxygen were measured in the field. This investigation was conducted mainly under low water flow conditions of the river, while a limited number of campaigns were under high flow conditions due to precipitation events. The concentrations of major inorganic ions increased steadily toward the down-stream, resulting in approximately two times increase for the traveling distance of 100 km. They showed a seasonal variation that they were highest in the spring and lowest in the autumn when there were most concentrated precipitation events in a year. The constituents were mainly Na{sup +}, Ca{sup 2+}, SO{sub 4}{sup 2-} and HCO{sub 3}{sup -}, and were similar for every sampling locations and seasons. Concentrations of dissolved organic substances (carbon compounds) were lowest in the upstream and increased about twice in the downstream as well as major inorganic ions. Their level was 1-3 mg/l, which can be ranked as relatively lower in general values for fresh water environments. They were highest in the spring (average over the locations: 2.2 mg/l) and lowest in the autumn (1.3 mg/l) and also in the winter (1.3 mg/l). These results will be useful as a basic understanding of spatial and seasonal variations of river water chemistry, especially related to the organic substances which can bind with radionuclides to make a mobile complex. (author).

  19. Effects of water chemistry on arsenic removal from drinking water by electrocoagulation.

    Science.gov (United States)

    Wan, Wei; Pepping, Troy J; Banerji, Tuhin; Chaudhari, Sanjeev; Giammar, Daniel E

    2011-01-01

    Exposure to arsenic through drinking water poses a threat to human health. Electrocoagulation is a water treatment technology that involves electrolytic oxidation of anode materials and in-situ generation of coagulant. The electrochemical generation of coagulant is an alternative to using chemical coagulants, and the process can also oxidize As(III) to As(V). Batch electrocoagulation experiments were performed in the laboratory using iron electrodes. The experiments quantified the effects of pH, initial arsenic concentration and oxidation state, and concentrations of dissolved phosphate, silica and sulfate on the rate and extent of arsenic removal. The iron generated during electrocoagulation precipitated as lepidocrocite (γ-FeOOH), except when dissolved silica was present, and arsenic was removed by adsorption to the lepidocrocite. Arsenic removal was slower at higher pH. When solutions initially contained As(III), a portion of the As(III) was oxidized to As(V) during electrocoagulation. As(V) removal was faster than As(III) removal. The presence of 1 and 4 mg/L phosphate inhibited arsenic removal, while the presence of 5 and 20 mg/L silica or 10 and 50 mg/L sulfate had no significant effect on arsenic removal. For most conditions examined in this study, over 99.9% arsenic removal efficiency was achieved. Electrocoagulation was also highly effective at removing arsenic from drinking water in field trials conducted in a village in Eastern India. By using operation times long enough to produce sufficient iron oxide for removal of both phosphate and arsenate, the performance of the systems in field trials was not inhibited by high phosphate concentrations.

  20. Impact of long term wetting on pore water chemistry in a peat bog in Ontario, Canada

    Science.gov (United States)

    Schaper, Jonas; Blodau, Christian; Holger Knorr, Klaus

    2013-04-01

    Peatlands of the northern hemisphere store a remarkable amount of carbon but also contribute to global methane emissions. As large areas in the boreal and subarctic zone are considered to undergo significant climate change it is necessary to understand how these ecosystems react to altered environmental conditions. Since not only temperatures but also precipitation is likely to increase in these regions, it is of particular interest to understand the impact of raised water tables and changing local hydrological flow patterns on peatlands' carbon cycle. We chose a pristine bog that was partly flooded by a reservoir lake created 60 years ago in Ontario, Canada. Water management in the reservoir resulted in seasonal flooding, shifting hydrological flow patterns and vegetation gradients. The impact of partial flooding on pore water chemistry and DIC and CH4 concentrations were studied within surface peat layers. Samples were taken with pore water peepers along the vegetation- and flooding gradient. Turnover rates of DIC and methane were calculated from obtained concentration profiles and peat porosity under the assumption that transport is dominated by diffusion. Values of pH changed remarkably from 4 within the undisturbed bog part to almost 8 at the lake shore. Ca2+ and Mg2+ were the only ions that showed significant distribution patterns with readily increasing concentrations towards the lake water body. CH4 and DIC concentrations also increased towards the lake and peaked in around 100 cm depth right at the shore with maximum concentrations being 2766 μmol L-1 for CH4 and 7543 μmol L-1 for DIC, respectively. Turnover rates also increased towards the shore albeit some uncertainty lies in this finding as steady state condition required for calculations were probably not established and transport was not only dominated by diffusion. Maximum CH4 production rates were modeled to be 36 nmol cm-3 d-1 and maximum DIC production was calculated to 64 nmol cm-3 d-1. Ca2

  1. An Introduction to Boiler Water Chemistry for the Marine Engineer: A Text of Audio-Tutorial Instruction.

    Science.gov (United States)

    Schlenker, Richard M.; And Others

    Presented is a manuscript for an introductory boiler water chemistry course for marine engineer education. The course is modular, self-paced, audio-tutorial, contract graded and combined lecture-laboratory instructed. Lectures are presented to students individually via audio-tapes and 35 mm slides. The course consists of a total of 17 modules -…

  2. Improved prediction of vegetation composition in NW European softwater lakes by combining location, water and sediment chemistry

    DEFF Research Database (Denmark)

    Pulido Pérez, Cristina; Jensen, Kaj Sand; Lucassen, Esther C.H.E.T.;

    2012-01-01

    composition. This complex analysis can also account for high sediment variability in the littoral zone of individual lakes, by using site-specific physico-chemical sediment factors, and offer better predictions of vegetation composition when lake water chemistry is relatively homogeneous among lakes within...

  3. Enhanced Control of PWR Primary Coolant Water Chemistry Using Selective Separation Systems for Recovery and Recycle of Enriched Boric Acid

    Energy Technology Data Exchange (ETDEWEB)

    Ken Czerwinski; Charels Yeamans; Don Olander; Kenneth Raymond; Norman Schroeder; Thomas Robison; Bryan Carlson; Barbara Smit; Pat Robinson

    2006-02-28

    The objective of this project is to develop systems that will allow for increased nuclear energy production through the use of enriched fuels. The developed systems will allow for the efficient and selective recover of selected isotopes that are additives to power water reactors' primary coolant chemistry for suppression of corrosion attack on reactor materials.

  4. Preliminary assessment of water chemistry related to groundwater flooding in Wawarsing, New York, 2009-11

    Science.gov (United States)

    Brown, Craig J.; Eckhardt, David A.; Stumm, Frederick; Chu, Anthony

    2012-01-01

    Water-quality samples collected in an area prone to groundwater flooding in Wawarsing, New York, were analyzed and assessed to better understand the hydrologic system and to aid in the assessment of contributing water sources. Above average rainfall over the past decade, and the presence of a pressurized water tunnel that passes about 700 feet beneath Wawarsing, could both contribute to groundwater flooding. Water samples were collected from surface-water bodies, springs, and wells and analyzed for major and trace inorganic constituents, dissolved gases, age tracers, and stable isotopes. Distinct differences in chemistry exist between tunnel water and groundwater in unconsolidated deposits and in bedrock, and among groundwater samples collected from some bedrock wells during high head pressure and low head pressure of the Rondout-West Branch Tunnel. Samples from bedrock wells generally had relatively higher concentrations of sulfate (SO42-), strontium (Sr), barium (Ba), and lower concentrations of calcium (Ca) and bicarbonate (HCO3-), as compared to unconsolidated wells. Differences in stable-isotope ratios among oxygen-18 to oxygen-16 (δ18O), hydrogen-2 to hydrogen-1 (δ2H), sulfur-34 to sulfur-32(δ34S) of SO42-, Sr-87 to Sr-86 (87Sr/86Sr), and C-13 to C-12 (δ13C) of dissolved inorganic carbon (DIC) indicate a potential for distinguishing water in the Delaware-West Branch Tunnel from native groundwater. For example, 87Sr/86Sr ratios were more depleted in groundwater samples from most bedrock wells, as compared to samples from surface-water sources, springs, and wells screened in unconsolidated deposits in the study area. Age-tracer data provided useful information on pathways of the groundwater-flow system, but were limited by inherent problems with dissolved gases in bedrock wells. The sulfur hexafluoride (SF6) and (or) chlorofluorocarbons (CFCs) apparent recharge years of most water samples from wells screened in unconsolidated deposits and springs ranged

  5. Environmental chemistry. Seventh edition

    Energy Technology Data Exchange (ETDEWEB)

    Manahan, S.E. [Univ. of Missouri, Columbia, MO (United States)

    1999-11-01

    This book presents a basic understanding of environmental chemistry and its applications. In addition to providing updated materials in this field, the book emphasizes the major concepts essential to the practice of environmental chemistry. Topics of discussion include the following: toxicological chemistry; toxicological chemistry of chemical substances; chemical analysis of water and wastewater; chemical analysis of wastes and solids; air and gas analysis; chemical analysis of biological materials and xenobiotics; fundamentals of chemistry; and fundamentals of organic chemistry.

  6. Properties, performance and associated hazards of state-of-the-art durable water repellent (DWR) chemistry for textile finishing.

    Science.gov (United States)

    Holmquist, H; Schellenberger, S; van der Veen, I; Peters, G M; Leonards, P E G; Cousins, I T

    2016-05-01

    Following the phase-out of long-chain per- and polyfluoroalkyl substances (PFASs), the textile industry had to find alternatives for side-chain fluorinated polymer based durable water repellent (DWR) chemistries that incorporated long perfluoroalkyl side chains. This phase-out and subsequent substitution with alternatives has resulted in a market where both fluorinated and non-fluorinated DWRs are available. These DWR alternatives can be divided into four broad groups that reflect their basic chemistry: side-chain fluorinated polymers, silicones, hydrocarbons and other chemistries (includes dendrimer and inorganic nanoparticle chemistries). In this critical review, the alternative DWRs are assessed with regards to their structural properties and connected performance, loss and degradation processes resulting in diffuse environmental emissions, and hazard profiles for selected emitted substances. Our review shows that there are large differences in performance between the alternative DWRs, most importantly the lack of oil repellence of non-fluorinated alternatives. It also shows that for all alternatives, impurities and/or degradation products of the DWR chemistries are diffusively emitted to the environment. Our hazard ranking suggests that hydrocarbon based DWR is the most environmentally benign, followed by silicone and side-chain fluorinated polymer-based DWR chemistries. Industrial commitments to reduce the levels of impurities in silicone based and side-chain fluorinated polymer based DWR formulations will lower the actual risks. There is a lack of information on the hazards associated with DWRs, in particular for the dendrimer and inorganic nanoparticle chemistries, and these data gaps must be filled. Until environmentally safe alternatives, which provide the required performance, are available our recommendation is to choose DWR chemistry on a case-by-case basis, always weighing the benefits connected to increased performance against the risks to the

  7. Ground Water Chemistry Changes before Major Earthquakes and Possible Effects on Animals

    Science.gov (United States)

    Grant, Rachel A.; Halliday, Tim; Balderer, Werner P.; Leuenberger, Fanny; Newcomer, Michelle; Cyr, Gary; Freund, Friedemann T.

    2011-01-01

    Prior to major earthquakes many changes in the environment have been documented. Though often subtle and fleeting, these changes are noticeable at the land surface, in water, in the air, and in the ionosphere. Key to understanding these diverse pre-earthquake phenomena has been the discovery that, when tectonic stresses build up in the Earth’s crust, highly mobile electronic charge carriers are activated. These charge carriers are defect electrons on the oxygen anion sublattice of silicate minerals, known as positive holes, chemically equivalent to O− in a matrix of O2−. They are remarkable inasmuch as they can flow out of the stressed rock volume and spread into the surrounding unstressed rocks. Travelling fast and far the positive holes cause a range of follow-on reactions when they arrive at the Earth’s surface, where they cause air ionization, injecting massive amounts of primarily positive air ions into the lower atmosphere. When they arrive at the rock-water interface, they act as •O radicals, oxidizing water to hydrogen peroxide. Other reactions at the rock-water interface include the oxidation or partial oxidation of dissolved organic compounds, leading to changes of their fluorescence spectra. Some compounds thus formed may be irritants or toxins to certain species of animals. Common toads, Bufo bufo, were observed to exhibit a highly unusual behavior prior to a M6.3 earthquake that hit L’Aquila, Italy, on April 06, 2009: a few days before the seismic event the toads suddenly disappeared from their breeding site in a small lake about 75 km from the epicenter and did not return until after the aftershock series. In this paper we discuss potential changes in groundwater chemistry prior to seismic events and their possible effects on animals. PMID:21776211

  8. Evolution of water chemistry in natural acidic environments in Yangmingshan, Taiwan.

    Science.gov (United States)

    Ezoe, Yuka; Lin, Cheng-Huang; Noto, Masami; Watanabe, Yoshihiro; Yoshimura, Kazuhisa

    2002-08-01

    In Yangmingshan National Park, located in the northern part of the Taiwan Island, there is a very rare area where fish (Channa asiatica) live in spite of acid environments. The origin of the acid in local acid ponds and rivers and the evolution of the water chemistry are discussed on the basis of sulfur stable isotope ratios and chemical equilibria. One of the sources of the acid is sulfuric acid, which is derived from the oxidation of hydrogen sulfide in volcanic gas gushing out from fumaroles around the area and from acid deposition supplied from Taipei City. It is also derived from the oxidation of pyrite: the sulfur stable isotope ratios of delta 34S of +1@1000 to +4@1000 (relative to CDT) of sulfate in acid pond waters (pH 3-4) could be related to those of hydrogen sulfide in volcanic gas, pyrite in local pond sediments and soils, and sulfate in rain water. One acid source is sulfuric and hydrochloric acids arising in springs from geothermal activity: the delta 34S values were characterised by +13@1000 to +17@1000 sulfate-S, which was provided by a disproportionation reaction of sulfur dioxide in the depths. Another acid source could be the oxidation of iron(II). Under acidic conditions, the water-rock reaction gives rise to high concentrations of aluminium and iron. While flowing down surface streams, iron(II) is oxidised to iron(III) and then hydrolysed to cause further acidification under oxic conditions. The concentrations of iron and aluminium are controlled by redox and dissolution equilibria.

  9. Addressing the complexity of water chemistry in environmental fate modeling for engineered nanoparticles.

    Science.gov (United States)

    Sani-Kast, Nicole; Scheringer, Martin; Slomberg, Danielle; Labille, Jérôme; Praetorius, Antonia; Ollivier, Patrick; Hungerbühler, Konrad

    2015-12-01

    Engineered nanoparticle (ENP) fate models developed to date - aimed at predicting ENP concentration in the aqueous environment - have limited applicability because they employ constant environmental conditions along the modeled system or a highly specific environmental representation; both approaches do not show the effects of spatial and/or temporal variability. To address this conceptual gap, we developed a novel modeling strategy that: 1) incorporates spatial variability in environmental conditions in an existing ENP fate model; and 2) analyzes the effect of a wide range of randomly sampled environmental conditions (representing variations in water chemistry). This approach was employed to investigate the transport of nano-TiO2 in the Lower Rhône River (France) under numerous sets of environmental conditions. The predicted spatial concentration profiles of nano-TiO2 were then grouped according to their similarity by using cluster analysis. The analysis resulted in a small number of clusters representing groups of spatial concentration profiles. All clusters show nano-TiO2 accumulation in the sediment layer, supporting results from previous studies. Analysis of the characteristic features of each cluster demonstrated a strong association between the water conditions in regions close to the ENP emission source and the cluster membership of the corresponding spatial concentration profiles. In particular, water compositions favoring heteroaggregation between the ENPs and suspended particulate matter resulted in clusters of low variability. These conditions are, therefore, reliable predictors of the eventual fate of the modeled ENPs. The conclusions from this study are also valid for ENP fate in other large river systems. Our results, therefore, shift the focus of future modeling and experimental research of ENP environmental fate to the water characteristic in regions near the expected ENP emission sources. Under conditions favoring heteroaggregation in these

  10. Ground water chemistry changes before major earthquakes and possible effects on animals.

    Science.gov (United States)

    Grant, Rachel A; Halliday, Tim; Balderer, Werner P; Leuenberger, Fanny; Newcomer, Michelle; Cyr, Gary; Freund, Friedemann T

    2011-06-01

    Prior to major earthquakes many changes in the environment have been documented. Though often subtle and fleeting, these changes are noticeable at the land surface, in water, in the air, and in the ionosphere. Key to understanding these diverse pre-earthquake phenomena has been the discovery that, when tectonic stresses build up in the Earth's crust, highly mobile electronic charge carriers are activated. These charge carriers are defect electrons on the oxygen anion sublattice of silicate minerals, known as positive holes, chemically equivalent to O- in a matrix of O2-. They are remarkable inasmuch as they can flow out of the stressed rock volume and spread into the surrounding unstressed rocks. Travelling fast and far the positive holes cause a range of follow-on reactions when they arrive at the Earth's surface, where they cause air ionization, injecting massive amounts of primarily positive air ions into the lower atmosphere. When they arrive at the rock-water interface, they act as •O radicals, oxidizing water to hydrogen peroxide. Other reactions at the rock-water interface include the oxidation or partial oxidation of dissolved organic compounds, leading to changes of their fluorescence spectra. Some compounds thus formed may be irritants or toxins to certain species of animals. Common toads, Bufo bufo, were observed to exhibit a highly unusual behavior prior to a M6.3 earthquake that hit L'Aquila, Italy, on April 06, 2009: a few days before the seismic event the toads suddenly disappeared from their breeding site in a small lake about 75 km from the epicenter and did not return until after the aftershock series. In this paper we discuss potential changes in groundwater chemistry prior to seismic events and their possible effects on animals.

  11. Organic geochemistry and pore water chemistry of sediments from Mangrove Lake, Bermuda

    Science.gov (United States)

    Hatcher, P.G.; Simoneit, B.R.T.; MacKenzie, F.T.; Neumann, A.C.; Thorstenson, D.C.; Gerchakov, S.M.

    1982-01-01

    Mangrove Lake, Bermuda, is a small coastal, brackish-water lake that has accumulated 14 m of banded, gelatinous, sapropelic sediments in less than 104 yr. Stratigraphic evidence indicates that Mangrove Lake's sedimentary environment has undergone three major depositional changes (peat, freshwater gel, brackish-water gel) as a result of sea level changes. The deposits were examined geochemically in an effort to delineate sedimentological and diagenetic changes. Gas and pore water studies include measurements of sulfides, ammonia, methane, nitrogen gas, calcium, magnesium, chloride, alkalinity, and pH. Results indicate that sulfate reduction is complete, and some evidence is presented for bacterial denitrification and metal sulfide precipitation. The organic-rich sapropel is predominantly algal in origin, composed mostly of carbohydrates and insoluble macromolecular organic matter called humin with minor amounts of proteins, lipids, and humic acids. Carbohydrates and proteins undergo hydrolysis with depth in the marine sapropel but tend to be preserved in the freshwater sapropel. The humin, which has a predominantly aliphatic structure, increases linearly with depth and composes the greatest fraction of the organic matter. Humic acids are minor components and are more like polysaccharides than typical marine humic acids. Fatty acid distributions reveal that the lipids are of an algal and/or terrestrial plant source. Normal alkanes with a total concentration of 75 ppm exhibit two distribution maxima. One is centered about n-C22 with no odd/even predominance, suggestive of a degraded algal source. The other is centered at n-C31 with a distinct odd/even predominance indicative of a vascular plant origin. Stratigraphic changes in the sediment correlate to observed changes in the gas and pore water chemistry and the organic geochemistry. ?? 1982.

  12. Ground Water Chemistry Changes before Major Earthquakes and Possible Effects on Animals

    Directory of Open Access Journals (Sweden)

    Friedemann T. Freund

    2011-06-01

    Full Text Available Prior to major earthquakes many changes in the environment have been documented. Though often subtle and fleeting, these changes are noticeable at the land surface, in water, in the air, and in the ionosphere. Key to understanding these diverse pre-earthquake phenomena has been the discovery that, when tectonic stresses build up in the Earth’s crust, highly mobile electronic charge carriers are activated. These charge carriers are defect electrons on the oxygen anion sublattice of silicate minerals, known as positive holes, chemically equivalent to O– in a matrix of O2–. They are remarkable inasmuch as they can flow out of the stressed rock volume and spread into the surrounding unstressed rocks. Travelling fast and far the positive holes cause a range of follow-on reactions when they arrive at the Earth’s surface, where they cause air ionization, injecting massive amounts of primarily positive air ions into the lower atmosphere. When they arrive at the rock-water interface, they act as •O radicals, oxidizing water to hydrogen peroxide. Other reactions at the rock-water interface include the oxidation or partial oxidation of dissolved organic compounds, leading to changes of their fluorescence spectra. Some compounds thus formed may be irritants or toxins to certain species of animals. Common toads, Bufo bufo, were observed to exhibit a highly unusual behavior prior to a M6.3 earthquake that hit L’Aquila, Italy, on April 06, 2009: a few days before the seismic event the toads suddenly disappeared from their breeding site in a small lake about 75 km from the epicenter and did not return until after the aftershock series. In this paper we discuss potential changes in groundwater chemistry prior to seismic events and their possible effects on animals.

  13. "Click" and Olefin Metathesis Chemistry in Water at Room Temperature Enabled by Biodegradable Micelles.

    Science.gov (United States)

    Lipshutz, Bruce H; Bošković, Zarko; Crowe, Christopher S; Davis, Victoria K; Whittemore, Hannah C; Vosburg, David A; Wenzel, Anna G

    2013-11-12

    The two laboratory reactions focus on teaching several concepts associated with green chemistry. Each uses a commercial, nontoxic, and biodegradable surfactant, TPGS-750-M, to promote organic reactions within the lipophilic cores of nanoscale micelles in water. These experiments are based on work by K. Barry Sharpless (an azide-alkyne "click" reaction) and Robert Grubbs (an olefin cross-metathesis reaction); both are suitable for an undergraduate organic laboratory. The copper-catalyzed azide-alkyne [3+2] cycloaddition of benzyl azide and 4-tolylacetylene is very rapid: the triazole product is readily isolated by filtration and is characterized by thin-layer chromatography and melting point analysis. The ruthenium-catalyzed olefin cross-metathesis reaction of benzyl acrylate with 1-hexene is readily monitored by thin-layer chromatography and gas chromatography. The metathesis experiment comparatively evaluates the efficacy of a TPGS-750-M/water medium relative to a traditional reaction performed in dichloromethane (a common solvent used for olefin metathesis).

  14. “Click” and Olefin Metathesis Chemistry in Water at Room Temperature Enabled by Biodegradable Micelles

    Science.gov (United States)

    Lipshutz, Bruce H.; Bošković, Zarko; Crowe, Christopher S.; Davis, Victoria K.; Whittemore, Hannah C.; Vosburg, David A.; Wenzel, Anna G.

    2013-01-01

    The two laboratory reactions focus on teaching several concepts associated with green chemistry. Each uses a commercial, nontoxic, and biodegradable surfactant, TPGS-750-M, to promote organic reactions within the lipophilic cores of nanoscale micelles in water. These experiments are based on work by K. Barry Sharpless (an azide–alkyne “click” reaction) and Robert Grubbs (an olefin cross-metathesis reaction); both are suitable for an undergraduate organic laboratory. The copper-catalyzed azide–alkyne [3+2] cycloaddition of benzyl azide and 4-tolylacetylene is very rapid: the triazole product is readily isolated by filtration and is characterized by thin-layer chromatography and melting point analysis. The ruthenium-catalyzed olefin cross-metathesis reaction of benzyl acrylate with 1-hexene is readily monitored by thin-layer chromatography and gas chromatography. The metathesis experiment comparatively evaluates the efficacy of a TPGS-750-M/water medium relative to a traditional reaction performed in dichloromethane (a common solvent used for olefin metathesis). PMID:24324282

  15. Interactions between hydrology and water chemistry shape bacterioplankton biogeography across boreal freshwater networks.

    Science.gov (United States)

    Niño-García, Juan Pablo; Ruiz-González, Clara; Del Giorgio, Paul A

    2016-07-01

    Disentangling the mechanisms shaping bacterioplankton communities across freshwater ecosystems requires considering a hydrologic dimension that can influence both dispersal and local sorting, but how the environment and hydrology interact to shape the biogeography of freshwater bacterioplankton over large spatial scales remains unexplored. Using Illumina sequencing of the 16S ribosomal RNA gene, we investigate the large-scale spatial patterns of bacterioplankton across 386 freshwater systems from seven distinct regions in boreal Québec. We show that both hydrology and local water chemistry (mostly pH) interact to shape a sequential structuring of communities from highly diverse assemblages in headwater streams toward larger rivers and lakes dominated by fewer taxa. Increases in water residence time along the hydrologic continuum were accompanied by major losses of bacterial richness and by an increased differentiation of communities driven by local conditions (pH and other related variables). This suggests that hydrology and network position modulate the relative role of environmental sorting and mass effects on community assembly by determining both the time frame for bacterial growth and the composition of the immigrant pool. The apparent low dispersal limitation (that is, the lack of influence of geographic distance on the spatial patterns observed at the taxonomic resolution used) suggests that these boreal bacterioplankton communities derive from a shared bacterial pool that enters the networks through the smallest streams, largely dominated by mass effects, and that is increasingly subjected to local sorting of species during transit along the hydrologic continuum.

  16. REDOX CHEMISTRY OF MOLYBDENUM IN NATURAL WATERS AND ITS INVOLVEMENT IN BIOLOGICAL EVOLUTION

    Directory of Open Access Journals (Sweden)

    Deli eWang

    2012-12-01

    Full Text Available The transition element molybdenum (Mo possesses diverse valances (+II to +VI, and is involved in forming cofactors in more than 60 enzymes in biology. Redox switching of the element in these enzymes catalyzes a series of metabolic reactions in both prokaryotes and eukaryotes, and the element therefore plays a fundamental role in the global carbon, nitrogen, and sulfur cycling. In the present oxygenated waters, oxidized Mo(VI predominates thermodynamically, whilst reduced Mo species are mainly confined within specific niches including cytoplasm. Only recently has the reduced Mo(V been separated from Mo(VI in sulfidic mats and even in some reducing waters. Given the presence of reduced Mo(V in contemporary anaerobic habitats, it seems that reduced Mo species were present in the ancient reducing ocean (probably under both ferrigenous and sulfidic conditions, prompting the involvement of Mo in enzymes including nitrogenase and nitrate reductase. During the global transition to oxic conditions, reduced Mo species were constrained to specific anaerobic habitats, and efficient uptake systems of oxidized Mo(VI became a selective advantage both for prokaryotic and eukaryotic cells. Some prokaryotes are still able to directly utilize reduced Mo if any exists in ambient environments. In total, this mini-review describes the redox chemistry and biogeochemistry of Mo over the Earth’s history.

  17. Water-soluble chemistry and weathering characteristics of some tills in Western Dronning Maud Land, Antarctica

    Directory of Open Access Journals (Sweden)

    Lintinen, P.

    1997-12-01

    Full Text Available The water-soluble chemistry and weathering characteristics of tills were studied on three nunataks with differing bedrock characteristics in the Vestfjella and Heimefrontfjella areas of the Western Dronning Maud Land, Antarctica. The chemical analyses were performed using ion chromatography and ICP-AES. The relative weathering characteristics of the till surface boulders was assessed in study locations. No colour differences were observed in test pits dug in Basen and Utpostane nunataks at Vestfjella, whereas the till in Mygehenget nunatak at Heimefrontfjella has a pronounced soil profile in which the surface part has a banded rusty brown and light-coloured accumulations. The highest concentrations of readily soluble ions were recorded in the Mygehenget samples characterized by high (SO42- (5800-39000 ppm and Mg concentrations (540-6000 ppm, while the Basen samples had the highest concentrations of Fe2+(23-390 ppm, Al3+ (60-1000 ppm and Si4+ (23-1700 ppm and the Utpostane samples the lowest ones. The SO4/Na+, Na+/CI- and Mg2+/Na+ ratios for the samples differ markedly from those typically encountered in sea water. The presence of the highest concentrations of many of the analysed ions in the Mygehenget soil samples is in line with the advanced weathering of the surface boulders. The high Fe2+ , Si4+ and Al3+ concentrations in the Basen samples may be attributable to the weathering of olivine alteration products.

  18. Water chemistry in 179 randomly selected Swedish headwater streams related to forest production, clear-felling and climate.

    Science.gov (United States)

    Löfgren, Stefan; Fröberg, Mats; Yu, Jun; Nisell, Jakob; Ranneby, Bo

    2014-12-01

    From a policy perspective, it is important to understand forestry effects on surface waters from a landscape perspective. The EU Water Framework Directive demands remedial actions if not achieving good ecological status. In Sweden, 44 % of the surface water bodies have moderate ecological status or worse. Many of these drain catchments with a mosaic of managed forests. It is important for the forestry sector and water authorities to be able to identify where, in the forested landscape, special precautions are necessary. The aim of this study was to quantify the relations between forestry parameters and headwater stream concentrations of nutrients, organic matter and acid-base chemistry. The results are put into the context of regional climate, sulphur and nitrogen deposition, as well as marine influences. Water chemistry was measured in 179 randomly selected headwater streams from two regions in southwest and central Sweden, corresponding to 10 % of the Swedish land area. Forest status was determined from satellite images and Swedish National Forest Inventory data using the probabilistic classifier method, which was used to model stream water chemistry with Bayesian model averaging. The results indicate that concentrations of e.g. nitrogen, phosphorus and organic matter are related to factors associated with forest production but that it is not forestry per se that causes the excess losses. Instead, factors simultaneously affecting forest production and stream water chemistry, such as climate, extensive soil pools and nitrogen deposition, are the most likely candidates The relationships with clear-felled and wetland areas are likely to be direct effects.

  19. Using official map data on topography, wetlands and vegetation cover for prediction of stream water chemistry in boreal headwater catchments

    Directory of Open Access Journals (Sweden)

    J.-O. Andersson

    2009-04-01

    Full Text Available A large part of the spatial variation of stream water chemistry can be related to inputs from headwater streams. In order to understand and analyse the dominant processes taking place in small and heterogeneous catchments, accurate data with high spatial and temporal resolution is necessary. In most cases, the quality and resolution of available map data are considered too poor to be used in environmental assessments and modelling of headwater stream chemistry. In this study 18 forested catchments (1–4 km2 were selected within a 120×50 km region in the county of Värmland in western Sweden. The aim was to test if topographic and vegetation variables derived from official datasets were correlated to stream water chemistry, primarily the concentration of dissolved organic carbon (DOC, but also Al, Fe and Si content. GIS was used to analyse the elevation characteristics, generate topographic indices, and calculate the percentage of wetlands and a number of vegetation classes. The results clearly show that topography has a major influence on stream water chemistry. There were strong correlations between mean slope and percentage wetland, percentage wetland and DOC, mean slope and DOC, and a very strong correlation between mean topographic wetness index (TWI and DOC. The conclusion was that official topographic data, despite uncertain or of low quality and resolution, could be useful in the prediction of headwater DOC-concentration in boreal forested catchments.

  20. Pore water chemistry reveals gradients in mineral transformation across a model basaltic hillslope

    Science.gov (United States)

    Pohlmann, Michael; Dontsova, Katerina; Root, Robert; Ruiz, Joaquin; Troch, Peter; Chorover, Jon

    2016-06-01

    The extent of weathering incongruency during soil formation from rock controls local carbon and nutrient cycling in ecosystems, as well as the evolution of hydrologic flow paths. Prior studies of basalt weathering, including those that have quantified the dynamics of well-mixed, bench-scale laboratory reactors or characterized the structure and integrated response of field systems, indicate a strong influence of system scale on weathering rate and trajectory. For example, integrated catchment response tends to produce lower weathering rates than do well mixed reactors, but the mechanisms underlying these disparities remain unclear. Here we present pore water geochemistry and physical sensor data gathered during two controlled rainfall-runoff events on a large-scale convergent model hillslope mantled with 1 m uniform depth of granular basaltic porous media. The dense sampler and sensor array (1488 samplers and sensors embedded in 330 m3 of basalt) showed that rainfall-induced dissolution of basaltic glass produced supersaturation of pore waters with respect to multiple secondary solids including allophane, gibbsite, ferrihydrite, birnessite and calcite. The spatial distribution of saturation state was heterogeneous, suggesting an accumulation of solutes leading to precipitation of secondary solids along hydrologic flow paths. Rapid dissolution of primary silicates was widespread throughout the entire hillslope, irrespective of up-gradient flowpath length. However, coherent spatial variations in solution chemistry and saturation indices were observed in depth profiles and between distinct topographic regions of the hillslope. Colloids (110-2000 nm) enriched in iron (Fe), aluminum (Al), and phosphorus (P) were mobile in soil pore waters.

  1. Application, chemistry, and environmental implications of contaminant-immobilization amendments on agricultural soil and water quality.

    Science.gov (United States)

    Udeigwe, Theophilus K; Eze, Peter N; Teboh, Jasper M; Stietiya, Mohammed H

    2011-01-01

    Contaminants such as nitrogen (N), phosphorus (P), dissolved organic carbon (DOC), arsenic (As), heavy metals, and infectious pathogens are often associated with agricultural systems. Various soil and water remediation techniques including the use of chemical amendments have been employed to reduce the risks associated with these contaminants. This paper reviews the use of chemical amendments for immobilizing principal agricultural contaminants, the chemistry of contaminant immobilization, and the environmental consequences associated with the use of these chemical products. The commonly used chemical amendments were grouped into aluminum-, calcium-, and iron-containing products. Other products of interest include phosphorus-containing compounds and silicate clays. Mechanisms of contaminant immobilization could include one or a combination of the following: surface precipitation, adsorption to mineral surfaces (ion exchange and formation of stable complexes), precipitation as salts, and co-precipitation. The reaction pH, redox potential, clay minerals, and organic matter are potential factors that could control contaminant-immobilization processes. Reviews of potential environmental implications revealed that undesirable substances such as trace elements, fluoride, sulfate, total dissolved solids, as well as radioactive materials associated with some industrial wastes used as amendment could be leached to ground water or lost through runoff to receiving water bodies. The acidity or alkalinity associated with some of the industrial-waste amendments could also constitute a substantial environmental hazard. Chemical amendments could introduce elements capable of inducing or affecting the activities of certain lithotrophic microbes that could influence vital geochemical processes such as mineral dissolution and formation, weathering, and organic matter mineralization.

  2. Seasonal dynamics of water and air chemistry in an indoor chlorinated swimming pool.

    Science.gov (United States)

    Zare Afifi, Mehrnaz; Blatchley, Ernest R

    2015-01-01

    Although swimming is known to be beneficial in terms of cardiovascular health, as well as for some forms of rehabilitation, swimming is also known to present risks to human health, largely in the form of exposure to microbial pathogens and disinfection byproducts (DBPs). Relatively little information is available in the literature to characterize the seasonal dynamics of air and water chemistry in indoor chlorinated swimming pools. To address this issue, water samples were collected five days per week from an indoor chlorinated swimming pool facility at a high school during the academic year and once per week during summer over a fourteen-month period. The samples were analyzed for free and combined chlorine, urea, volatile DBPs, pH, temperature and total alkalinity. Membrane Introduction Mass Spectrometry (MIMS) was used to identify and measure the concentrations of eleven aqueous-phase volatile DBPs. Variability in the concentrations of these DBPs was observed. Factors that influenced variability included bather loading and mixing by swimmers. These compounds have the ability to adversely affect water and air quality and human health. A large fraction of the existing literature regarding swimming pool air quality has focused on trichloramine (NCl₃). For this work, gas-phase NCl₃ was analyzed by an air sparging-DPD/KI method. The results showed that gas-phase NCl₃ concentration is influenced by bather loading and liquid-phase NCl₃ concentration. Urea is the dominant organic-N compound in human urine and sweat, and is known to be an important precursor for producing NCl₃ in swimming pools. Results of daily measurements of urea indicated a link between bather load and urea concentration in the pool.

  3. Dissolved organic matter conformation and its interaction with pyrene as affected by water chemistry and concentration.

    Science.gov (United States)

    Pan, Bo; Ghosh, Saikat; Xing, Baoshan

    2008-03-01

    Water chemistry and concentration of dissolved organic matter (DOM) have been reported to affect DOM conformation and binding properties with hydrophobic organic contaminants (HOCs). However, relationship between DOM conformation and its binding properties remains unclear. We designed a multibag equilibration system (MBES) to investigate the variation of carbon-normalized sorption coefficients (K(DOC)) of pyrene at different DOM concentrations based on an identical free solute concentration at different pHs and in the presence of Al ions. In addition, we studied the conformation of DOM under different conditions via atomic force microscopy (AFM) imaging, dynamic light scattering, and zeta potential measurements. Zeta potential measurements indicated that intra- and intermolecular interaction was facilitated at low pH or with the presence of Al ions, and a more organized molecular aggregate (such as a micelle-like structure) could form, thus, enhancing K(DOC). As DOM concentration increased, DOM molecular aggregation was promoted in a way reducing K(DOC). This research is a first attempt to correlate DOM conformation with K(DOC). Aggregation of DOM molecules resulting from increased zeta potential (less negative) generally led to an increased K(DOC). Further study in this area will provide valuable information on HOC-DOM interactions, thus, leading to more accurate predictions of K(DOC).

  4. Mineralogy and pore water chemistry of a boiler ash from a MSW fluidized-bed incinerator.

    Science.gov (United States)

    Bodénan, F; Guyonnet, D; Piantone, P; Blanc, P

    2010-07-01

    This paper presents an investigation of the mineralogy and pore water chemistry of a boiler ash sampled from a municipal solid waste fluidized-bed incinerator, subject to 18 months of dynamic leaching in a large percolation column experiment. A particular focus is on the redox behaviour of Cr(VI) in relation to metal aluminium Al(0), as chromium may represent an environmental or health hazard. The leaching behaviour and interaction between Cr(VI) and Al(0) are interpreted on the basis of mineralogical evolutions observed over the 18-month period and of saturation indices calculated with the geochemical code PhreeqC and reviewed thermodynamic data. Results of mineralogical analyses show in particular the alteration of mineral phases during leaching (e.g. quartz and metal aluminium grains), while geochemical calculations suggest equilibria of percolating fluids with respect to specific mineral phases (e.g. monohydrocalcite and aluminium hydroxide). The combination of leaching data on a large scale and mineralogical analyses document the coupled leaching behaviour of aluminium and chromium, with chromium appearing in the pore fluids in its hexavalent and mobile state once metal aluminium is no longer available for chromium reduction.

  5. Results from an in-situ pore water chemistry experiment in opalinus clay: evidence of microbially mediated anaerobic redox processes

    Energy Technology Data Exchange (ETDEWEB)

    Wersin, P.; Mettler, S. [NAGRA - National Cooperative for the Disposal of Radioactive Waste, Wettingen (Switzerland); Canniere, P. de [SCK-CEN, Mol (Belgium); Pearson, F.J. [Ground-Water Geochemistry, New Bern (United States); Gaucher, E. [BRGM, 75 - Paris (France); Hohener, P. [BioRem, CH (Switzerland); Eichinger, L. [Hydroisotop, Schweitenkirchen (Germany); Mader, U. [Bern Univ., CH (Switzerland); Vinsot, A. [Agence Nationale pour la Gestion des Dechets Radioactifs (ANDRA), 92 - Chatenay Malabry (France); Gabler, H.E. [Federal Institute for Geosciences and Natural Resources (BGR), Hannover (Germany); Hama, K. [JNC - Japan Nuclear Cycle Development Institute (JNC) Horonobe (Japan); Hernan, P. [ENRESA, Madrid (Spain)

    2005-07-01

    Low permeability argillaceous rocks are considered potential host rocks for radioactive waste disposal in a number of countries. Characterisation of pore water chemistry is important for assessing radionuclide behaviour, but technically challenging because of intimate clay-water association. The application of different techniques, such as in-situ extraction, squeezing and leaching has led to improved understanding. However, because of potential experimental artefacts (e.g. degassing of CO{sub 2}, ingress of O{sub 2} ), significant uncertainties remain, especially with regard to pH/pCO{sub 2} and Eh conditions. Moreover, the pore water chemistry may be perturbed by the drilling procedure itself, thus leading to oxidation and biodegradation effects. In order to reduce uncertainties mentioned above and to gain deeper insight into geochemical processes regulating pH and Eh, the internationally supported Pore water Chemistry (PC) experiment was started at the Mont Terri Rock Laboratory in 2002. The basis of the study is an in-situ experiment employing the diffusive equilibration method. The field study was complemented with lab investigations which include chemical analyses for principal inorganic solutes, for reduced sulphur species and for a variety of specific organic compounds, gas measurements of core samples and a core infiltration study based on advective displacement. (authors)

  6. A teacher as researcher study of high school chemistry student ideas about the particulate nature of water

    Science.gov (United States)

    Kruckeberg, Robert Fredrick

    The objective of this study was to advance the pedagogical content knowledge base for teaching high school chemistry by conducting qualitative research on students' scientific understanding of water prior to, during, and after formal instruction on the particulate nature of matter. The study was conducted within a constructivist theoretical framework, with an emphasis on John Dewey's pragmatic social constructivism. The teacher-as-researcher conducted three sets of clinical interviews based on three related contexts: representation of water in the liquid state, interaction of water with a solute, and water vaporizing and condensing. Interviews and class work were analyzed to determine the extent to which students used the particulate nature of matter to reorganize their understanding of water. Findings present student responses in terms of four different aspects of the particulate model, where students frequently emphasized certain aspects of the model to the exclusion of others. These aspects were identified as "Simple Particles," "Mechanical Kinetic," "Differential Chemical", and "Electrostatic Interactive." Students exhibited significant difficulty in extending micro-mechanical aspects of the model into an electrostatic-interactive understanding of water. Applications of the particulate model were often highly context dependent. Students showed a variety of unique, alternative interpretations of the particulate nature of water that were supported by rich qualitative interview responses. Student difficulties understanding the particulate nature of water were attributed to alternative conceptions prior to instruction as well as the content and sequencing of the traditional biology-chemistry-physics science curriculum. The study recommends changes in curriculum sequencing, improved instruction in the nature of science and scientific models, and the need for introducing students to ideas in physics, especially electrostatics, prior to the study of introductory

  7. Degradation of Environmental Contaminants with Water-Soluble Cobalt Catalysts: An Integrative Inorganic Chemistry Investigation

    Science.gov (United States)

    Evans, Alexandra L.; Messersmith, Reid E.; Green, David B.; Fritsch, Joseph M.

    2011-01-01

    We present an integrative laboratory investigation incorporating skills from inorganic chemistry, analytical instrumentation, and physical chemistry applied to a laboratory-scale model of the environmental problem of chlorinated ethylenes in groundwater. Perchloroethylene (C[subscript 2]Cl[subscript 4], PCE) a common dry cleaning solvent,…

  8. Water physics and chemistry data from moored current meter and bottle casts in the Coastal Waters of New Jersey as part of the Mesa New York Bight (MESA - NYB) project, 05 November 1973 to 06 June 1974 (NODC Accession 7500931)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Coastal Waters of New Jersey from November 5, 1973 to June 6,...

  9. Water physics and chemistry data from moored current meter and bottle casts in the Coastal Waters of New Jersey as part of the Mesa New York Bight (MESA - NYB) project, 27 August 1973 - 27 November 1974 (NODC Accession 7600777)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Coastal Waters of New Jersey from August 27, 1973 to November 7,...

  10. Water physics and chemistry data from moored current meter and bottle casts in the Coastal Waters of New Jersey as part of the Mesa New York Bight (MESA - NYB) project, 21 May 1963 - 08 July 1975 (NODC Accession 7601561)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Coastal Waters of New Jersey from May 21, 1963 to July 8, 1975....

  11. Water physics and chemistry data from moored current meter and bottle casts in the Coastal Waters of New Jersey as part of the Mesa New York Bight (MESA - NYB) project, 08 March 1974 - 13 May 1974 (NODC Accession 7501210)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Coastal Waters of New Jersey from March 8, 1974 to May 13, 1974....

  12. Water physics and chemistry data from moored current meter and bottle casts in the Coastal Waters of New Jersey as part of the Mesa New York Bight (MESA - NYB) project, 10 April 1978 - 09 August 1978 (NODC Accession 7900249)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Coastal Waters of New Jersey from April 10, 1978 to August 9,...

  13. Water physics and chemistry data from moored current meter and bottle casts in the Coastal Waters of New Jersey as part of the Mesa New York Bight (MESA - NYB) project from 12 April 1976 - 13 September 1976 (NODC Accession 7700770)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Coastal Waters of New Jersey from April 12, 1976 to September 13,...

  14. Water physics and chemistry data from moored current meter and bottle casts in the Coastal Waters of New Jersey as part of the Mesa New York Bight (MESA - NYB) project, 09 April 1979 - 23 August 1979 (NODC Accession 8100440)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Coastal Waters of New Jersey from April 9, 1979 to August 23,...

  15. Adventures in STEM: Lessons in Water Chemistry From Elementary School to Graduate School

    Science.gov (United States)

    Dittrich, T. M.

    2014-12-01

    I will present the accumulation of over 10 years of experience teaching STEM subjects to students ranging from 1st grade to graduate school. I was fortunate to gain a lot of valuable teaching experience while in graduate school in Boulder, CO and so many of my experiences center on opportunities for connecting with students in the field in CO. 3rd-5th grade field hikes - While helping at Jamestown Elementary School, I led hikes with a 3-5th grade class to an abandoned flourospar mine where the students were able to pick up beautiful purple fluorite crystals from the ground while discussing how mining works. During the hike back, we used field meters to measure the pH and conductivity of the stream and discussed the need to balance society's need for metals with the harmful effects of acid mine drainage. 9th, 10th grade STEM Academy at Skyline High School - During an NSF-sponsored fellowship, I had the opportunity to teach a STEM class to 9th and 10th graders where we used the engineering design process to a) design a tool to help a handicapped 3rd grader use the drinking fountain by herself and b) design a treatment system for cleaning up acid mine drainage. Undergraduate and Graduate Environmental Water Chemistry Field Trip - Students had the opportunity to tour two local mine sites to collect contaminated water that would be used in class for alkalinity titrations and pH, sulfate, and hardness measurements. They also collected water samples upstream and at multiple points downstream of a wastewater treatment plan and measured and graphed the dissolved oxygen "sag" in the river. My main teaching philosophy has two parts: 1) assume the students know nothing and 2) assume the students are even smarter than you think you are. This informs my approach to field trips by always starting from the beginning, but also not oversimplifying the topic. 1st graders on their best day can be very similar to graduate students on their worst.

  16. The Irminger Sea and the Iceland Sea time series measurements of sea water carbon and nutrient chemistry 1983–2008

    Directory of Open Access Journals (Sweden)

    J. Olafsson

    2010-03-01

    Full Text Available This paper describes the ways and means of assembling and quality controling the Irminger Sea and Iceland Sea time-series biogeochemical data which are included in the CARINA data set. The Irminger Sea and the Iceland Sea are hydrographically different regions where measurements of sea water carbon and nutrient chemistry were started in 1983. The sampling is seasonal, four times a year. The carbon chemistry is studied with measurements of the partial pressure of carbon dioxide in seawater, pCO2, and total dissolved inorganic carbon, TCO2. The carbon chemistry data are for surface waters only until 1991 when water column sampling was initiated. Other measured parameters are salinity, dissolved oxygen and the inorganic nutrients nitrate, phosphate and silicate. Because of the CARINA criteria for secondary quality control, depth >1500 m, the IRM-TS could not be included in the routine QC and the IS-TS only in a limited way. However, with the information provided here, the quality of the data can be assessed, e.g. on the basis of the results obtained with the use of reference materials.

  17. The Irminger Sea and the Iceland Sea time series measurements of sea water carbon and nutrient chemistry 1983–2006

    Directory of Open Access Journals (Sweden)

    J. Olafsson

    2009-10-01

    Full Text Available This paper describes the ways and means of assembling and quality controling the Irminger Sea and Iceland Sea time-series biogeochemical data which are included in the CARINA data set. The Irminger Sea and the Iceland Sea are hydrographically different regions where measurements of sea water carbon and nutrient chemistry were started in 1983. The sampling is seasonal, four times a year. The carbon chemistry is studied with measurements of the partial pressure of carbon dioxide in seawater, pCO2, and total dissolved inorganic carbon, TCO2. The carbon chemistry data are for surface waters only until 1994 when water column sampling was initiated. Other measured parameters are salinity, dissolved oxygen and the inorganic nutrients nitrate, phosphate and silicate. Because of the CARINA criteria for secondary quality control, depth >1500 m, the IRM-TS could not be included in the routine QC and the IS-TS only in a limited way. However, with the information provided here, the quality of the data can be assessed e.g. on the basis of the results obtained with the use of reference materials.

  18. Groundwater, surface-water, and water-chemistry data, Black Mesa area, northeastern Arizona—2012–2013

    Science.gov (United States)

    Macy, Jamie P.; Truini, Margot

    2016-03-02

    The Navajo (N) aquifer is an extensive aquifer and the primary source of groundwater in the 5,400-square-mile Black Mesa area in northeastern Arizona. Availability of water is an important issue in northeastern Arizona because of continued water requirements for industrial and municipal use by a growing population and because of low precipitation in the arid climate of the Black Mesa area. Precipitation in the area typically is between 6 and 14 inches per year.The U.S. Geological Survey water-monitoring program in the Black Mesa area began in 1971 and provides information about the long-term effects of groundwater withdrawals from the N aquifer for industrial and municipal uses. This report presents results of data collected as part of the monitoring program in the Black Mesa area from January 2012 to September 2013. The monitoring program includes measurements of (1) groundwater withdrawals, (2) groundwater levels, (3) spring discharge, (4) surface-water discharge, and (5) groundwater chemistry.In calendar year 2012, total groundwater withdrawals were 4,010 acre-ft, industrial withdrawals were 1,370 acre-ft, and municipal withdrawals were 2,640 acre-ft. Total withdrawals during 2012 were about 45 percent less than total withdrawals in 2005 because of Peabody Western Coal Company’s discontinued use of water to transport coal in a coal slurry pipeline. From 2011 to 2012 total withdrawals decreased by 10 percent; industrial withdrawals decreased by approximately 1 percent, and total municipal withdrawals decreased by 15 percent.From 2012 to 2013, annually measured water levels in the Black Mesa area declined in 6 of 16 wells that were available for comparison in the unconfined areas of the N aquifer, and the median change was 0.8 feet. Water levels declined in 5 of 16 wells measured in the confined area of the aquifer. The median change for the confined area of the aquifer was 0.3 feet. From the prestress period (prior to 1965) to 2013, the median water

  19. Groundwater, surface-water, and water-chemistry data, Black Mesa area, northeastern Arizona: 2011-2012

    Science.gov (United States)

    Macy, Jamie P.; Unema, Joel A.

    2014-01-01

    The Navajo (N) aquifer is an extensive aquifer and the primary source of groundwater in the 5,400-square-mile Black Mesa area in northeastern Arizona. Availability of water is an important issue in northeastern Arizona because of continued water requirements for industrial and municipal use by a growing population and because of low precipitation in the arid climate of the Black Mesa area. Precipitation in the area typically is between 6 and 14 inches per year. The U.S. Geological Survey water-monitoring program in the Black Mesa area began in 1971 and provides information about the long-term effects of groundwater withdrawals from the N aquifer for industrial and municipal uses. This report presents results of data collected as part of the monitoring program in the Black Mesa area from January 2011 to September 2012. The monitoring program includes measurements of (1) groundwater withdrawals, (2) groundwater levels, (3) spring discharge, (4) surface-water discharge, and (5) groundwater chemistry. In 2011, total groundwater withdrawals were 4,480 acre-ft, industrial withdrawals were 1,390 acre-ft, and municipal withdrawals were 3,090 acre-ft. Total withdrawals during 2011 were about 39 percent less than total withdrawals in 2005 because of Peabody Western Coal Company’s discontinued use of water to transport coal in a slurry. From 2010 to 2011 total withdrawals increased by 11 percent; industrial withdrawals increased by approximately 19 percent, and total municipal withdrawals increased by 8 percent. From 2011 to 2012, annually measured water levels in the Black Mesa area declined in 8 of 15 wells that were available for comparison in the unconfined areas of the N aquifer, and the median change was -0.1 feet. Water levels declined in 9 of 18 wells measured in the confined area of the aquifer. The median change for the confined area of the aquifer was 0.0 feet. From the prestress period (prior to 1965) to 2012, the median water-level change for 34 wells in both

  20. Understanding flood-induced water chemistry variability extracting temporal patterns with the LDA method

    Science.gov (United States)

    Aubert, A. H.; Tavenard, R.; Emonet, R.; De Lavenne, A.; Malinowski, S.; Guyet, T.; Quiniou, R.; Odobez, J.; Merot, P.; Gascuel-odoux, C.

    2013-12-01

    Studying floods has been a major issue in hydrological research for years, both in quantitative and qualitative hydrology. Stream chemistry is a mix of solutes, often used as tracers, as they originate from various sources in the catchment and reach the stream by various flow pathways. Previous studies (for instance (1)) hypothesized that stream chemistry reaction to a rainfall event is not unique but varies seasonally, and according to the yearly meteorological conditions. Identifying a typology of flood temporal chemical patterns is a way to better understand catchment processes at the flood and seasonal time scale. We applied a probabilistic model (Latent Dirichlet Allocation or LDA (2)) mining recurrent sequential patterns from a dataset of floods. A set of 472 floods was automatically extracted from a daily 12-year long record of nitrate, dissolved organic carbon, sulfate and chloride concentrations. Rainfall, discharge, water table depth and temperature are also considered. Data comes from a long-term hydrological observatory (AgrHys, western France) located at Kervidy-Naizin. From each flood, a document has been generated that is made of a set of "hydrological words". Each hydrological word corresponds to a measurement: it is a triplet made of the considered variable, the time at which the measurement is made (relative to the beginning of the flood), and its magnitude (that can be low, medium or high). The documents and the number of pattern to be mined are used as input data to the LDA algorithm. LDA relies on spotting co-occurrences (as an alternative to the more traditional study of correlation) between words that appear within the flood documents. It has two nice properties that are its ability to easily deal with missing data and its additive property that allows a document to be seen as a mixture of several flood patterns. The output of LDA is a set of patterns easily represented in graphics. These patterns correspond to typical reactions to rainfall

  1. Disentangling the effects of water chemistry and substratum structure on moss-dwelling unicellular and multicellular micro-organisms in spring-fens

    Directory of Open Access Journals (Sweden)

    Michal HORSÁK

    2011-09-01

    Full Text Available Water chemistry is known to be one of the most important factors controlling species composition of many macro-organisms in wetlands. It is unclear to what extent micro-organisms respond to water chemistry as compared to chemistry-mediated substratum structure. We explored how the assemblages of different groups of micro-organisms in bryophyte tufts of spring-fens were determined by water chemistry and substratum structure. The aim was to compare unicellular autotrophic diatoms, unicellular heterotrophic testate amoebae and multicellular heterotrophic monogonont rotifers. Assemblages of all three groups showed a strong compositional gradient correlated with water pH and conductivity, calcium concentration and dominance of Sphagnum. While a second strong gradient in species composition of diatoms and testate amoebae was explained by factors such as substratum structure and water content, that of rotifers remained unexplained. Unlike the other two groups, testate amoeba assemblages were significantly determined by phosphates. Nitrates and iron were important species composition determinants for diatoms. Rotifers differed from the other groups in that they did not respond significantly to silica, iron or nutrients. When variation caused by substratum characteristics and water chemistry were partitioned out, testate amoebae were controlled more by substratum, while rotifers and diatoms were controlled more by water chemistry. Variation explained by individual effects of substratum or water chemistry, as compared to shared effects, was much lower for rotifers than for testate amoebae and diatoms. Our results show that, in semi-terrestrial ecosystems, pH and calcium concentrations are generally the main drivers of variation in species composition of unicellular and multicellular microorganisms, mirroring well described patterns for macro-organisms, providing support for general ecological hypotheses. Other water chemistry variables differed between

  2. Trait modality distribution of aquatic macrofauna communities as explained by pesticides and water chemistry.

    Science.gov (United States)

    Ieromina, O; Musters, C J M; Bodegom, P M; Peijnenburg, W J G M; Vijver, M G

    2016-08-01

    Analyzing functional species' characteristics (species traits) that represent physiological, life history and morphological characteristics of species help understanding the impacts of various stressors on aquatic communities at field conditions. This research aimed to study the combined effects of pesticides and other environmental factors (temperature, dissolved oxygen, dissolved organic carbon, floating macrophytes cover, phosphate, nitrite, and nitrate) on the trait modality distribution of aquatic macrofauna communities. To this purpose, a field inventory was performed in a flower bulb growing area of the Netherlands with significant variation in pesticides pressures. Macrofauna community composition, water chemistry parameters and pesticide concentrations in ditches next to flower bulb fields were determined. Trait modalities of nine traits (feeding mode, respiration mode, locomotion type, resistance form, reproduction mode, life stage, voltinism, saprobity, maximum body size) likely to indicate pesticides impacts were analyzed. According to a redundancy analysis, phosphate -and not pesticides- constituted the main factor structuring the trait modality distribution of aquatic macrofauna. The functional composition could be ascribed for 2-4 % to pesticides, and for 3-11 % to phosphate. The lack of trait responses to pesticides may indicate that species may have used alternative strategies to adapt to ambient pesticides stress. Biomass of animals exhibiting trait modalities related to feeding by predation and grazing, presence of diapause form or dormancy, reproduction by free clutches and ovoviviparity, life stage of larvae and pupa, was negatively correlated to the concentration of phosphate. Hence, despite the high pesticide pollution in the area, variation in nutrient-related stressors seems to be the dominant driver of the functional composition of aquatic macrofauna assembly in agricultural ditches.

  3. NWFSC OA facility water chemistry - Ocean acidification species exposure experimental facility

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — We have developed a unique facility for conducting high-quality experiments on marine organisms in seawater with controlled carbon chemistry conditions. The...

  4. Role of Water in Electron-Initiated Processes and Radical Chemistry: Issues and Scientific Advances

    Energy Technology Data Exchange (ETDEWEB)

    Garrett, Bruce C.; Dixon, David A.; Camaioni, Donald M.; Chipman, Daniel M.; Johnson, Mark A.; Jonah, Charles D.; Kimmel, Greg A.; Miller, John H.; Rescigno, Tom; Rossky, Peter J.; Xantheas, Sotiris S.; Colson, Steve D.; Laufer, Allan H.; Ray, Douglas; Barbara, Paul F.; Bartels, David M.; Bowen, Kit H.; Becker, Kurt H.; Bradforth, Stephen E.; Carmichael, Ian; Coe, James V.; Corrales, L. Rene; Cowin, James P.; Dupuis, Michel; Eisenthal, Kenneth B.; Franz, James A.; Gutowski, Maciej S.; Jordon, Kenneth D.; Kay, Bruce D.; La Verne, Jay A.; Lymar, Sergei V.; Madey, Theodore E.; Mccurdy, C. W.; Meisel, Dan; Mukamel, Shaul; Nilsson, Anders R.; Orlando, Thomas M.; Petrik, Nikolay G.; Pimblott, Simon M.; Rustad, James R.; Schenter, Gregory K.; Singer, Sherwin J.; Tokmakoff, Andrei; Wang, Lai-Sheng; Wittig, Curt; Zwier, Timothy S.

    2005-01-12

    An understanding of electron-initiated processes in aqueous systems and the subsequent radical chemistry these processes induce is significant in such diverse fields as waste remediation and environmental cleanup, radiation processing, nuclear reactors, and medical diagnosis and therapy. We review the state of the art in the physical chemistry and chemical physics of electron-initiated processes in aqueous systems and raise critical research issues and fundamental questions that remain unanswered.

  5. Water physics and chemistry data from bottle casts from the DELAWARE from 10 May 1967 to 01 June 1967 (NODC Accession 7000769)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected from bottle casts from the DELAWARE from 10 May 1967 to 01 June 1967. Data were submitted by the National Marine...

  6. Water physics and chemistry data from bottle casts from the AQUALAB from 14 October 1968 to 11 December 1968 (NODC Accession 7100270)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected from bottle casts from the AQUALAB from 14 October 1968 to 11 December 1968. Data were submitted by the Southern...

  7. Water physics and chemistry data from bottle casts from the MISS FLETA from the 14 August 1962 to 06 December 1962 (NODC Accession 6900648)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected from bottle casts from the MISS FLETA from 14 August 1962 to 06 December 1962. Data were submitted by the Rosenstiel...

  8. Water physics and chemistry data from STD casts from THELMA DALE II and other platforms from 09 August 1954 to 05 March 1959 (NODC Accession 7101380)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected from STD casts from THELMA DALE II and other platforms from 09 August 1954 to 05 March 1959. Data were submitted by...

  9. Hydrology and water chemistry of the Benton Lake basin with emphasis on the fate of dissolved solids at Benton Lake National Wildlife Refuge, west-central Montana

    Data.gov (United States)

    US Fish and Wildlife Service, Department of the Interior — This report is on a hydro geochemical study of the Benton Lake basin, in Benton Lake National Wildlife Refige. Toe hydrology and water chemistry of the Benton Lake...

  10. Water physics and chemistry data from bottle casts from the CHESAPEAKE L/S and other platforms from 28 November 1955 to 31 December 1956 (NODC Accession 6800101)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected from bottle casts from the CHESAPEAKE L/S and other platforms from 28 November 1955 to 31 December 1956. Data were...

  11. Water physics and chemistry data from bottle casts from the AMIGO as part of the SEAGRANT project from 19 January 1972 to 20 April 1973 (NODC Accession 7400540)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected from bottle casts from the AMIGO from 19 January 1972 to 20 April 1973. Data were submitted by the Moss Landing...

  12. Water physics and chemistry data from bottle casts from the MICMAC R/V from the 28 January 1970 to 21 April 1970 (NODC Accession 7100666)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected from bottle casts from the MICMAC Stanford R/V from 28 January 1970 to 21 April 1970. Data were submitted by the...

  13. High temporal resolution water chemistry information for catchment understanding and management

    Science.gov (United States)

    Reaney, S. M.; Deasy, C.; Ockenden, M.; Perks, M.; Quinton, J.

    2013-12-01

    Many rivers and lakes are currently not meeting their full ecological potential due to environmental pressures including non-point source pollution from the catchment. These pressures include sediment, nitrogen and phosphorus from agriculture and other sources. Each of these pollutants is transferred through the landscape with different hydrological processes and along different pathways. Therefore, to effectively select and spatially target mitigation actions in the landscape, an understanding of the dominant hydrological processes and dynamics which are causing the transfer of material is required. Recent advances in environmental monitoring have enabled the collection of new rich datasets with a high temporal sampling frequency. In the UK, these techniques have been implemented in the Defra Demonstration Test Catchments project and with Natural England for targeted site investigations. Measurements include weather, hydrological flows, sediment, oxygen isotopes, nitrogen and phosphorus from a combination of in-field labs, water chemistry sondes and storm samplers. The detailed time series data can then be analysed to give insights into catchment processes through the analysis of the measured process dynamics. For example, evidence of the transfer of material along surface (or pipe) flow paths can be found from the co-incident timing of the sediment and flow record, or the timing of temperature variations after a storm event can give insight into the contribution of shallow groundwater. Given this evidence of catchment hydrological dynamics it is possible to determine the probable pathways which are transferring pollutants and hence it is possible to select suitable mitigation options in the landscape to improve the river or lake. For example, evidence of a pollutant transfer occurring as shallow soil flows suggests that buffer strips would not be an effective solution since these measures intercept surface pathways. Information on catchment residence time not

  14. Ditch blocking, water chemistry and organic carbon flux: evidence that blanket bog restoration reduces erosion and fluvial carbon loss.

    Science.gov (United States)

    Wilson, Lorraine; Wilson, Jared; Holden, Joseph; Johnstone, Ian; Armstrong, Alona; Morris, Michael

    2011-05-01

    The potential for restoration of peatlands to deliver benefits beyond habitat restoration is poorly understood. There may be impacts on discharge water quality, peat erosion, flow rates and flood risk, and nutrient fluxes. This study aimed to assess the impact of drain blocking, as a form of peatland restoration, on an upland blanket bog, by measuring water chemistry and colour, and loss of both dissolved (DOC) and particulate organic carbon (POC). The restoration work was designed to permit the collection of a robust experimental dataset over a landscape scale, with data covering up to 3 years pre-restoration and up to 3 years post-restoration. An information theoretic approach to data analyses provided evidence of a recovery of water chemistry towards more 'natural' conditions, and showed strong declines in the production of water colour. Drain blocking led to increases in the E4:E6 ratio, and declines in specific absorbance, suggesting that DOC released from blocked drains consisted of lighter, less humic and less decomposed carbon. Whilst concentrations of DOC showed slight increases in drains and streams after blocking, instantaneous yields of both DOC and POC declined markedly in streams over the first year post-restoration. Attempts were made to estimate total annual fluvial organic carbon fluxes for the study site, and although errors around these estimates remain considerable, there is strong evidence of a large reduction in aquatic organic carbon flux from the peatland following drain-blocking. Potential mechanisms for the observed changes in water chemistry and organic carbon release are discussed, and we highlight the need for more detailed information, from more sites, to better understand the full impacts of peatland restoration on carbon storage and release.

  15. Hydrogeologic framework refinement, ground-water flow and storage, water-chemistry analyses, and water-budget components of the Yuma area, southwestern Arizona and southeastern California

    Science.gov (United States)

    Dickinson, Jesse E.; Land, Michael; Faunt, Claudia C.; Leake, S.A.; Reichard, Eric G.; Fleming, John B.; Pool, D.R.

    2006-01-01

    The ground-water and surface-water system in the Yuma area in southwestern Arizona and southeastern California is managed intensely to meet water-delivery requirements of customers in the United States, to manage high ground-water levels in the valleys, and to maintain treaty-mandated water-quality and quantity requirements of Mexico. The following components in this report, which were identified to be useful in the development of a ground-water management model, are: (1) refinement of the hydrogeologic framework; (2) updated water-level maps, general ground-water flow patterns, and an estimate of the amount of ground water stored in the mound under Yuma Mesa; (3) review and documentation of the ground-water budget calculated by the Bureau of Reclamation, U.S. Department of the Interior (Reclamation); and (4) water-chemistry characterization to identify the spatial distribution of water quality, information on sources and ages of ground water, and information about the productive-interval depths of the aquifer. A refined three-dimensional digital hydrogeologic framework model includes the following hydrogeologic units from bottom to top: (1) the effective hydrologic basement of the basin aquifer, which includes the Pliocene Bouse Formation, Tertiary volcanic and sedimentary rocks, and pre-Tertiary metamorphic and plutonic rocks; (2) undifferentiated lower units to represent the Pliocene transition zone and wedge zone; (3) coarse-gravel unit; (4) lower, middle, and upper basin fill to represent the upper, fine-grained zone between the top of the coarse-gravel unit and the land surface; and (5) clay A and clay B. Data for the refined model includes digital elevation models, borehole lithology data, geophysical data, and structural data to represent the geometry of the hydrogeologic units. The top surface of the coarse-gravel unit, defined by using borehole and geophysical data, varies similarly to terraces resulting from the down cutting of the Colorado River. Clay A

  16. Impact of volcanic plume emissions on rain water chemistry during the January 2010 Nyamuragira eruptive event: implications for essential potable water resources.

    Science.gov (United States)

    Cuoco, Emilio; Tedesco, Dario; Poreda, Robert J; Williams, Jeremy C; De Francesco, Stefano; Balagizi, Charles; Darrah, Thomas H

    2013-01-15

    On January 2, 2010 the Nyamuragira volcano erupted lava fountains extending up to 300 m vertically along an ~1.5 km segment of its southern flank cascading ash and gas on nearby villages and cities along the western side of the rift valley. Because rain water is the only available potable water resource within this region, volcanic impacts on drinking water constitutes a major potential hazard to public health within the region. During the 2010 eruption, concerns were expressed by local inhabitants about water quality and feelings of physical discomfort (e.g. nausea, bloating, indigestion, etc.) after consuming rain water collected after the eruption began. We present the elemental and ionic chemistry of drinking water samples collected within the region on the third day of the eruption (January 5, 2010). We identify a significant impact on water quality associated with the eruption including lower pH (i.e. acidification) and increases in acidic halogens (e.g. F(-) and Cl(-)), major ions (e.g. SO(4)(2-), NH(4)(+), Na(+), Ca(2+)), potentially toxic metals (e.g. Al(3+), Mn(2+), Cd(2+), Pb(2+), Hf(4+)), and particulate load. In many cases, the water's composition significantly exceeds World Health Organization (WHO) drinking water standards. The degree of pollution depends upon: (1) ash plume direction and (2) ash plume density. The potential negative health impacts are a function of the water's pH, which regulates the elements and their chemical form that are released into drinking water.

  17. Aespoe Hard Rock Laboratory. Prototype Repository. Analyses of microorganisms, gases and water chemistry in buffer and backfill, 2009

    Energy Technology Data Exchange (ETDEWEB)

    Lydmark, Sara (Microbial Analytics Sweden AB (Sweden))

    2010-09-15

    The Prototype repository is an international project to build and study a full-scale model of the planned Swedish final repository for spent nuclear fuel. The Prototype repository differs from a real storage in that it is drained. For example, this makes the swelling pressure lower in the Prototype repository compared with a real storage. The project is being conducted at the Aespoe Hard Rock Laboratory (HRL) in crystalline rock at a depth of approximately 450 m. A monitoring programme is investigating the evolution of the water chemistry, gas, and microbial activity at the site, and one of the specific aims is to monitor the microbial consumption of oxygen in situ in the Prototype repository. This document describes the results of the analyses of microbes, gases, and chemistry inside and outside the Prototype in 2009. Hydrogen, helium, nitrogen, oxygen, carbon monoxide, carbon dioxide, methane, ethane, and ethene were analysed in the following sampling points in the Prototype repository: KBU10001, KBU10002, KBU10004, KBU10006, KBU10008, KFA01 and KFA04. Where the sampling points in the Prototype delivered pore water, the water was analysed for amount of ATP (i.e., the biovolume), cultivable heterotrophic aerobic bacteria (CHAB), sulphate-reducing bacteria (SRB), methane-oxidizing bacteria (MOB), autotrophic acetogens (AA) and in some cases iron-reducing bacteria (IRB). Cultivation methods were also compared with qPCR molecular techniques to evaluate these before next year's decommission of the Prototype repository. The collected pore water from the Prototype repository was subject to chemistry analysis (as many analyses were conducted as the amount of water allowed). In addition, groundwater from two borehole sections in the rock surrounding the Prototype was analysed regarding its gas composition, microbiology and redox. Chemistry data from a previous investigation of the groundwater outside the Prototype repository were compared with the pore water

  18. Influence of changing water sources and mineral chemistry on the everglades ecosystem

    Science.gov (United States)

    McCormick, P.V.; Harvey, J.W.; Crawford, E.S.

    2011-01-01

    Human influences during the previous century increased mineral inputs to the Florida Everglades by changing the sources and chemistry of surface inflows. Biogeochemical responses to this enrichment include changes in the availability of key limiting nutrients such as P, the potential for increased turnover of nutrient pools due to accelerated plant decomposition, and increased rates of mercury methylation associated with sulfate enrichment. Mineral enrichment has also been linked to the loss of sensitive macrophyte species, although dominant Everglades species appear tolerant of a broad range of mineral chemistry. Shifts in periphyton community composition and function provide an especially sensitive indicator of mineral enrichment. Understanding the influence of mineral chemistry on Everglades processes and biota may improve predictions of ecosystem responses to ongoing hydrologic restoration efforts and provide guidelines for protecting remaining mineral-poor areas of this peatland. Copyright ?? 2011 Taylor & Francis Group, LLC.

  19. The ion chemistry of surface and ground waters in the Taklimakan Desert of Tarim Basin, western China

    Institute of Scientific and Technical Information of China (English)

    ZHU BingQi; YANG XiaoPing

    2007-01-01

    The physio-chemical and chemical features of water in natural conditions are controlled by the weathering of bedrocks, local climate, landforms and other geo-environmental parameters. In order to understand the characteristics of water and the origins of the dissolved loads in the rivers and in the ground waters of the Taklimakan Desert, western China, we studied the ions in the water samples collected from rivers and wells. We collected water samples from four rivers (Keriya River, Cele River, Tumiya River and Yulongkashi River) in the southern desert and ground water samples from many parts of the desert. Major cations and anions were measured using ion-chromatograph and titration with HCl. The total dissolved solids (TDS), pH and conductivity were examined on site by a portable multi-parameter analyzer. The data show that the water in the rivers of southern Taklimakan is still of fresh water quality and slight alkalinity, although the TDS is comparatively higher than that of many other rivers of the world. The ground water is fresh to slightly saline, with TDS a little higher than that of river water in the study area. The concentration of ions is slightly different between the four rivers in the southern Taklimakan. However, the chemistries of ground water in all samples are to a large degree controlled by sodium and chloride. The ions in the ground water are concluded to be mainly from dissolving of evaporites, consistent with the dry climate in the region, whereas the ions in the rivers are mainly from rock weathering. Low-level human imprints are recognized in the ground water samples also.

  20. Water-Chemistry Evolution and Modeling of Radionuclide Sorption and Cation Exchange during Inundation of Frenchman Flat Playa

    Energy Technology Data Exchange (ETDEWEB)

    Hershey, Ronald; Cablk, Mary; LeFebre, Karen; Fenstermaker, Lynn; Decker, David

    2013-08-01

    valuable information about chemical processes occurring during inundation as the water disappeared. Important observations from water-chemistry analyses included: 1) total dissolved solids (TDS) and chloride ion (Cl-) concentrations were very low (TDS: < 200 mg/L and Cl-: < 3.0 mg/L, respectively) for all water samples regardless of time or areal extent; 2) all dissolved constituents were at concentrations well below what might be expected for evaporating shallow surface waters on a playa, even when 98 to 99 percent of the water had disappeared; 3) the amount of evaporation for the last water samples collected at the end of inundation, estimated with the stable isotopic ratios δ2H or δ18O, was approximately 60 percent; and 4) water samples analyzed by gamma spectroscopy did not show any man-made radioactivity; however, the short scanning time (24 hours) and relative chemical diluteness of the water samples (TDS ranged between 39 and 190 mg/L) may have contributed to none being detected. Additionally, any low-energy beta emitting radionuclides would not have been detected by gamma spectroscopy. From these observations, it was apparent that a significant portion of water on the playa did not evaporate, but rather infiltrated into the subsurface (approximately 40 percent). Consistent with this water chemistry-based conclusion is particle-size analysis of two archived Frenchman Flat playa soils samples, which showed low clay content in the near surface soil that also suggested infiltration. Infiltration of water from the playa during inundation into the subsurface does not necessarily imply that groundwater recharge is occurring, but it does provide a mechanism for moving residual radionuclides downward into the subsurface of Frenchman Flat playa. Water-mineral geochemical reactions were modeled so that changes in the water chemistry could be identified and the extent of reactions quantified. Geochemical modeling showed that evaporation; equilibrium with atmospheric carbon

  1. Water chemistry, seepage investigation, streamflow, reservoir storage, and annual availability of water for the San Juan-Chama Project, northern New Mexico, 1942-2010

    Science.gov (United States)

    McKean, Sarah E.; Anderholm, Scott K.

    2014-01-01

    The Albuquerque Bernalillo County Water Utility Authority supplements the municipal water supply for the Albuquerque metropolitan area, in central New Mexico, with surface water diverted from the Rio Grande. The U.S. Geological Survey, in cooperation with the Albuquerque Bernalillo County Water Utility Authority, undertook this study in which water-chemistry data and historical streamflow were compiled and new water-chemistry data were collected to characterize the water chemistry and streamflow of the San Juan-Chama Project (SJCP). Characterization of streamflow included analysis of the variability of annual streamflow and comparison of the theoretical amount of water that could have been diverted into the SJCP to the actual amount of water that was diverted for the SJCP. Additionally, a seepage investigation was conducted along the channel between Azotea Tunnel Outlet and the streamflow-gaging station at Willow Creek above Heron Reservoir to estimate the magnitude of the gain or loss in streamflow resulting from groundwater interaction over the approximately 10-mile reach. Generally, surface-water chemistry varied with streamflow throughout the year. Streamflow ranged from high flow to low flow on the basis of the quantity of water diverted from the Rio Blanco, Little Navajo River, and Navajo River for the SJCP. Vertical profiles of the water temperature over the depth of the water column at Heron Reservoir indicated that the reservoir is seasonally stratified. The results from the seepage investigations indicated a small amount of loss of streamflow along the channel. Annual variability in streamflow for the SJCP was an indication of the variation in the climate parameters that interact to contribute to streamflow in the Rio Blanco, Little Navajo River, Navajo River, and Willow Creek watersheds. For most years, streamflow at Azotea Tunnel Outlet started in March and continued for approximately 3 months until the middle of July. The majority of annual streamflow

  2. The impact of river infiltration on the chemistry of shallow groundwater in a reclaimed water irrigation area

    Science.gov (United States)

    Yin, Shiyang; Wu, Wenyong; Liu, Honglu; Bao, Zhe

    2016-10-01

    Reclaimed water reuse is an effective method of alleviating agricultural water shortages, which entails some potential risks for groundwater. In this study, the impacts of wastewater reuse on groundwater were evaluated by combination of groundwater chemistry and isotopes. In reclaimed water infiltration, salt composition was affected not only by ion exchange and dissolution equilibrium but also by carbonic acid equilibrium. The dissolution and precipitation of calcites and dolomites as well as exchange and adsorption between Na and Ca/Mg were simultaneous, leading to significant changes in Na/Cl, (Ca + Mg)/Cl, electrical conductivity (EC) and sodium adsorption ratio (SAR). The reclaimed water was of the Na-Mg-Ca-HCO3-Cl type, and groundwater recharged by reclaimed water was of the Na-Mg-HCO3 and Mg-Na-HCO3 types. The hydrogeological conditions characterized by sand-clay alternation led to both total nitrogen (TN) and total phosphorus (TP) removal efficiencies > 95%, and there was no significant difference in those contents between aquifers recharged by precipitation and reclamation water. > 40 years of long-term infiltration and recharge from sewage and reclaimed water did not cause groundwater contamination by nitrogen, phosphorus and heavy metals. These results indicate that characteristics of the study area, such as the lithologic structure with sand-clay alternation, relatively thick clay layer, and relatively large groundwater depth have a significant role in the high vulnerability.

  3. Inorganic ground-water chemistry at an experimental New Albany Shale (Devonian-Mississippian) in situ gasification site

    Science.gov (United States)

    Branam, T.D.; Comer, J.B.; Shaffer, N.R.; Ennis, M.V.; Carpenter, S.H.

    1991-01-01

    Experimental in situ gasification of New Albany Shale (Devonian-Mississippian) has been conducted in Clark County. Analyses of ground water sampled from a production well and nine nearby monitoring wells 3 months after a brief in situ gasification period revealed changes in water chemistry associated with the gasification procedure. Dissolved iron, calcium and sulphate in ground water from the production well and wells as much as 2 m away were significantly higher than in ground water from wells over 9 m away. Dissolved components in the more distant wells are in the range of those in regional ground water. Thermal decomposition of pyrite during the gasification process generated the elevated levels of iron and sulphate in solution. High concentrations of calcium indicate buffering by dissolution of carbonate minerals. While iron quickly precipitates, calcium and sulphate remain in the ground water. Trends in the concentration of sulphate show that altered ground water migrated mostly in a south-westerly direction from the production well along natural joints in the New Albany Shale. ?? 1991.

  4. Direct Measurement of Cloud Condensation Nuclei Chemistry using a New Microfluidic Instrument During the CalWater 2011 Campaign

    Science.gov (United States)

    Noblitt, S. D.; Roberts, G. C.; Corrigan, C.; Creamean, J.; Collins, D. B.; Cahill, J. F.; Prather, K. A.; Collett, J. L.; Henry, C.

    2011-12-01

    The CalWater 2011 campaign took place in the California Sierra Nevada with the objective of determining the effects atmospheric rivers and aerosols have on California precipitation. To meet this goal, the role of chemistry on atmospheric aerosols' ability to act as cloud condensation nuclei (CCN) needed to be evaluated because not all aerosols are CCN active. To date, direct measurement of ambient CCN chemistry has been difficult or unobtainable because of the difficulty in obtaining a well-defined CCN population, small aerosol masses, and low measurement flow rates. To address this need, a miniature CCN collector was employed that directly deposits CCN-active aerosol into an aqueous sample solution in a microfluidic device. Microchip electrophoresis (MCE) then performs chemical analysis on the soluble CCN components, and concentrations of water-soluble inorganic anions were obtained. Additional instruments were run alongside the CCN-MCE system to obtain a more complete characterization of the aerosol, including MCE coupled to a collector for all water condensation nuclei (WCN), two aerosol time-of-flight mass spectrometers (ATOFMS), optical CCN counters, condensation particle counters, and aerosol sizing instrumentation. The work discussed here will describe the operation of the CCN-MCE instrument and show the preliminary results obtained for CCN chemistry measurements at the Sugar Pine Reservoir during CalWater 2011. The prototype CCN-MCE analyzer permits online monitoring at a single, constant supersaturation. The outlet stream of the CCN system inertially impacts wetted CCN particles into a buffer-filled sample reservoir for immediate electrophoretic analysis, requiring CCN-MCE system collects aerosols at ~0.05 lpm and deposits them into ~20 μL of solution, providing detection limits of ~0.1 μg per cubic meter with 10 min of sampling. Because of the low (mostly rural) aerosol concentrations monitored at the Sugar Pine Reservoir, a poorer time resolution of ~1

  5. The springs of Lake Patzcuaro: chemistry, salt-balance, and implications for the water balance of the lake

    Energy Technology Data Exchange (ETDEWEB)

    Bischoff, James L.; Israde-Alcantara, Isabel; Garduno-Monroy, Victor H.; Shanks III, Wayne C

    2004-11-01

    Lake Patzcuaro, the center of the ancient Tarascan civilization located in the Mexican altiplano west of the city of Morelia, has neither river input nor outflow. The relatively constant lake-salinity over the past centuries indicates the lake is in chemical steady state. Springs of the south shore constitute the primary visible input to the lake, so influx and discharge must be via sub-lacustrine ground water. The authors report on the chemistry and stable isotope composition of the springs, deeming them representative of ground-water input. The springs are dominated by Ca, Mg and Na, whereas the lake is dominated by Na. Combining these results with previously published precipitation/rainfall measurements on the lake, the authors calculate the chemical evolution from spring water to lake water, and also calculate a salt balance of the ground-water-lake system. Comparing Cl and {delta}{sup 18}O compositions in the springs and lake water indicates that 75-80% of the spring water is lost evaporatively during evolution toward lake composition. During evaporation Ca and Mg are lost from the water by carbonate precipitation. Each liter of spring water discharging into the lake precipitates about 18.7 mg of CaCO{sub 3}. Salt balance calculations indicate that ground water input to the lake is 85.9 x 10{sup 6} m{sup 3}/a and ground water discharge from the lake is 23.0 x 10{sup 6} m{sup 3}/a. Thus, the discharge is about 27% of the input, with the rest balanced by evaporation. A calculation of time to reach steady-state ab initio indicates that the Cl concentration of the present day lake would be reached in about 150 a.

  6. The springs of Lake Pátzcuaro: chemistry, salt-balance, and implications for the water balance of the lake

    Science.gov (United States)

    Bischoff, James L.; Israde-Alcántara, Isabel; Garduno-Monroy, Victor H.; Shanks, Wayne C.

    2004-01-01

    Lake Pa??tzcuaro, the center of the ancient Tarascan civilization located in the Mexican altiplano west of the city of Morelia, has neither river input nor outflow. The relatively constant lake-salinity over the past centuries indicates the lake is in chemical steady state. Springs of the south shore constitute the primary visible input to the lake, so influx and discharge must be via sub-lacustrine ground water. The authors report on the chemistry and stable isotope composition of the springs, deeming them representative of ground-water input. The springs are dominated by Ca, Mg and Na, whereas the lake is dominated by Na. Combining these results with previously published precipitation/rainfall measurements on the lake, the authors calculate the chemical evolution from spring water to lake water, and also calculate a salt balance of the ground-water-lake system. Comparing Cl and ??18O compositions in the springs and lake water indicates that 75-80% of the spring water is lost evaporatively during evolution toward lake composition. During evaporation Ca and Mg are lost from the water by carbonate precipitation. Each liter of spring water discharging into the lake precipitates about 18.7 mg of CaCO3. Salt balance calculations indicate that ground water input to the lake is 85.9??106 m3/a and ground water discharge from the lake is 23.0??106 m3/a. Thus, the discharge is about 27% of the input, with the rest balanced by evaporation. A calculation of time to reach steady-state ab initio indicates that the Cl concentration of the present day lake would be reached in about 150 a. ?? 2004 Elsevier Ltd. All rights reserved.

  7. Conducting water chemistry of the secondary coolant circuit of VVER-based nuclear power plant units constructed without using copper containing alloys

    Science.gov (United States)

    Tyapkov, V. F.

    2014-07-01

    The secondary coolant circuit water chemistry with metering amines began to be put in use in Russia in 2005, and all nuclear power plant units equipped with VVER-1000 reactors have been shifted to operate with this water chemistry for the past seven years. Owing to the use of water chemistry with metering amines, the amount of products from corrosion of structural materials entering into the volume of steam generators has been reduced, and the flow-accelerated corrosion rate of pipelines and equipment has been slowed down. The article presents data on conducting water chemistry in nuclear power plant units with VVER-1000 reactors for the secondary coolant system equipment made without using copper-containing alloys. Statistical data are presented on conducting ammonia-morpholine and ammonia-ethanolamine water chemistries in new-generation operating power units with VVER-1000 reactors with an increased level of pH. The values of cooling water leaks in turbine condensers the tube system of which is made of stainless steel or titanium alloy are given.

  8. Characterization of the hydrology, water chemistry, and aquatic communities of selected springs in the St. Johns River Water Management District, Florida, 2004

    Science.gov (United States)

    Phelps, G.G.; Walsh, Stephen J.; Gerwig, Robert M.; Tate, William B.

    2006-01-01

    The hydrology, water chemistry, and aquatic communities of Silver Springs, De Leon Spring, Gemini Springs, and Green Spring in the St. Johns River Water Management District, Florida, were studied in 2004 to provide a better understanding of each spring and to compile data of potential use in future water-management decisions. Ground water that discharges from these and other north-central Florida springs originates from the Upper Floridan aquifer of the Floridan aquifer system, a karstic limestone aquifer that extends throughout most of the State's peninsula. This report summarizes data about flow, water chemistry, and aquatic communities, including benthic invertebrates, fishes, algae, and aquatic macrophytes collected by the U.S. Geological Survey, the St. Johns River Water Management District, and the Florida Department of Environmental Protection during 2004, as well as some previously collected data. Differences in water chemistry among these springs reflect local differences in water chemistry in the Upper Floridan aquifer. The three major springs sampled at the Silver Springs group (the Main Spring, Blue Grotto, and the Abyss) have similar proportions of cations and anions but vary in nitrate and dissolved oxygen concentrations. Water from Gemini Springs and Green Spring has higher proportions of sodium and chloride than the Silver Springs group. Water from De Leon Spring also has higher proportions of sodium and chloride than the Silver Springs group but lower proportions of calcium and bicarbonate. Nitrate concentrations have increased over the period of record at all of the springs except Green Spring. Compounds commonly found in wastewater were found in all the springs sampled. The most commonly detected compound was the insect repellant N,N'-diethyl-methyl-toluamide (DEET), which was found in all the springs sampled except De Leon Spring. The pesticide atrazine and its degradate 2-chloro-4-isopropylamino-6-amino-s-triazine (CIAT) were detected in water

  9. Characterizing interactions between surface water and groundwater in the Jialu River basin using major ion chemistry and stable isotopes

    Directory of Open Access Journals (Sweden)

    L. Yang

    2012-11-01

    Full Text Available The Jialu River, a secondary tributary of the Huaihe River, has been severely contaminated from major contaminant sources, such as a number of untreated or lightly treated sewage waste in some cities. Groundwater along the river is not an isolated component of the hydrologic system, but is instead connected with the surface water. This study aims to investigate temporal and spatial variations in water chemistry affected by humans and to characterize the relationships between surface water (e.g. reservoirs, lakes and rivers and groundwater near the river in the shallow Quaternary aquifer. Concentration of Cl in north Zhengzhou City increased prominently due to the discharge of a large amount of domestic water. Nitrate and potassium show maximum concentrations in groundwater in Fugou County. These high levels can be attributed to the use of a large quantity of fertilizer over this region. Most surface water appeared to be continuously recharged from the surrounding groundwater (regional wells based on comparison surface water with groundwater levels, stable-isotopes and major ion signatures. However, the groundwater of a transitional well (location SY3 seemed to be recharged by river water via bank infiltration in September 2010. Fractional contributions of river water to the groundwater were calculated based on isotopic and chemical data using a mass-balance approach. Results show that the groundwater was approximately composed of 60–70% river water. These findings should be useful for a better understanding of hydrogeological processes at the river-aquifer interface and ultimately benefit water management in the future.

  10. Does water chemistry affect the dietary uptake and toxicity of silver nanoparticles by the freshwater snail Lymnaea stagnalis?

    Science.gov (United States)

    López-Serrano Oliver, Ana; Croteau, Marie-Noële; Stoiber, Tasha L.; Tejamaya, Mila; Römer, Isabella; Lead, Jamie R.; Luoma, Samuel N.

    2014-01-01

    Silver nanoparticles (AgNPs) are widely used in many applications and likely released into the aquatic environment. There is increasing evidence that Ag is efficiently delivered to aquatic organisms from AgNPs after aqueous and dietary exposures. Accumulation of AgNPs through the diet can damage digestion and adversely affect growth. It is well recognized that aspects of water quality, such as hardness, affect the bioavailability and toxicity of waterborne Ag. However, the influence of water chemistry on the bioavailability and toxicity of dietborne AgNPs to aquatic invertebrates is largely unknown. Here we characterize for the first time the effects of water hardness and humic acids on the bioaccumulation and toxicity of AgNPs coated with polyvinyl pyrrolidone (PVP) to the freshwater snail Lymnaea stagnalis after dietary exposures. Our results indicate that bioaccumulation and toxicity of Ag from PVP-AgNPs ingested with food are not affected by water hardness and by humic acids, although both could affect interactions with the biological membrane and trigger nanoparticle transformations. Snails efficiently assimilated Ag from the PVP-AgNPs mixed with diatoms (Ag assimilation efficiencies ranged from 82 to 93%). Rate constants of Ag uptake from food were similar across the entire range of water hardness and humic acid concentrations. These results suggest that correcting regulations for water quality could be irrelevant and ineffective where dietary exposure is important.

  11. Microelectrodes Based investigation of the Impacts of Water Chemistry on Copper and Iron Corrosion

    Science.gov (United States)

    The effect of bulk drinking water quality on copper and iron pipe corrosion has been extensively studied. Despite past research, many have argued that bulk water quality does not necessarily reflect water quality near the water-metal interface and that such knowledge is necessary...

  12. DIWA trademark. AREVA's approach of intelligent computer-aided support of water chemistry monitoring in power plants

    Energy Technology Data Exchange (ETDEWEB)

    Fandrich, Joerg [AREVA NP GmbH, Erlangen (Germany)

    2011-07-01

    The complexity of power plant operation makes stringent demands on the chemical quality of the coolant in process systems and loops. Optimal water chemistry ensures high corrosion resistance of these systems and is thus essential for safe and economic long term plant operation. The market offers a huge variety of commercial software packages for water chemistry control. Most of these computer programs have to be considered as data analysis or, respectively, data acquisition programs. Some of them require manual data input (Laboratory Information Management Systems), others are capable of performing a fully automated data acquisition. However, the plant operator typically is left alone with the actual interpretation of all collected and validated data, which would be the main characteristic feature of an analysis (or monitoring) system. The data validation is typical being performed by means of numerical methods in the broadest sense. This activity requires a long working experience and specific skills by the plant chemistry operator. True diagnostic systems need to be significantly more advanced. They contain the capability of data interpretation and derivation of specific diagnoses. This is combined with additional explanations on how the diagnoses were derived. Additionally, further recommendations are offered on how to proceed to reach the normal operational behavior as soon as possible. AREVA's DIWA trademark system features a fuzzy logic expert system that is based on expert knowledge. It is built on symptoms, which are combined in rules as part of the fuzzy tool set. These components can be edited without programming knowledge, which significantly reduces training efforts. It makes the system more robust, more compact and simpler compared to other so-called expert systems. DIWA trademark represents the knowledge in a natural way, in which other conventional expert system may have difficulties or need a larger set of rule algorithms. (orig.)

  13. Analysis of meteorological data and water chemistry of Latir Lakes, Taos County, New Mexico, 1985-88

    Science.gov (United States)

    Anderholm, S.K.; Roybal, R.G.; Risser, D.W.; Somers, Georgene

    1994-01-01

    Data were analyzed to determine the chemistry of atmospheric deposition and water of the Latir Lakes in Taos County New Mexico, from 1985 to 1988. The Latir Lakes consist of a series of nine paternoster lakes that range in altitude from 11,061 to 11,893 feet above sea level. The pH of wet precipitation generally ranged from 4.6 to 5.5 and the specific conductance of wet precipitation ranged from 1 to 18 microsiemens per centimeter at 25 degrees Celsius from December 1985 through September 1988. Snowpack chemistry data indicate a change in the specific conductance, pH, and alkalinity of the snowpack from month to month. The dominant cation in the snowpack is calcium, and the dominant anions are nitrate and sulfate. The samples having the smallest values of specific conductance generally did not contain measurable alkalinity. When the snowpack starts to melt in the spring, specific conductance of the entire snowpack decreases, consistent with the hypothesis that the initial fluid draining from the snowpack transports a large amount of dissolved material out of the snowpack. Water chemistries in the Latir Lakes are similar although specific conductance increases downstream from lake 9 to lake 1. Calcium is the dominant cation and the ions that produce alkalinity are the dominant anions. Concentrations of sodium, magnesium, chloride, and sulfate do not vary substantially from year to year or during the year in a particular lake. Alkalinity and calcium concentration, however, do vary from year to year and during the year. The pH of outflow from the Latir Lakes varies from lake to lake and from year to year. In 1986, the range in pH in the lakes was less than 1 unit in mid-June, but was greater than 2.5 units by late October. The pH generally was larger than 7.0 in all of the lakes and was as large as 9.9 in several of the lakes during the period of study. The pH of outflow water generally increases from early spring to late summer in the Latir Lakes, and snowmelt does

  14. The effects of human land use on flow regime and water chemistry of headwater streams in the highlands of Chiapas

    Directory of Open Access Journals (Sweden)

    Castillo M.M.

    2013-03-01

    Full Text Available We studied the effects of land use changes on flow regime and water chemistry of headwater streams in the highlands of Chiapas, a region in southern Mexico that has experienced high rates of deforestation in the last decades. Samples for water chemistry were collected and discharge was measured between September 2007 and August 2008 at eight streams that differed in the land uses of their riparian and catchment areas, including streams draining protected forested areas. Streams with high forest cover (>70% in their catchments maintained flow through the year. Streams draining more disturbed catchments exhibited reduced or no flow for 4 − 6 months during the dry season. Nitrate concentrations were lower at streams draining forested catchments while highest concentrations were measured where conventional agriculture covered a high proportion of the catchment and riparian zone. Highest phosphorus concentrations occurred at the catchment where poultry manure was applied as fertilizer. Differences between forest streams and those draining disturbed areas were correlated with the proportion of forest and agriculture in the riparian zone. Variation in stream variables among sampling dates was lower at the forest sites than at the more disturbed study streams. Conversion of forest into agriculture and urban areas is affecting flow regime and increasing nutrient concentrations, although the magnitude of the impacts are influenced by the type of agricultural practices and the alteration of the riparian zone.

  15. Analysis of Pipe Wall-thinning Caused by Water Chemistry Change in Secondary System of Nuclear Power Plant

    Energy Technology Data Exchange (ETDEWEB)

    Yun, Hun; Hwang, Kyeongmo [KEPCO E and C, Gimcheon (Korea, Republic of); Moon, Seung-Jae [Hanyang University, Seoul (Korea, Republic of)

    2015-12-15

    Pipe wall-thinning by flow-accelerated corrosion (FAC) is a significant and costly damage of secondary system piping in nuclear power plants (NPPs). All NPPs have their management programs to ensure pipe integrity from wall-thinning. This study analyzed the pipe wall-thinning caused by changing the amine, which is used for adjusting the water chemistry in the secondary system of NPPs. The pH change was analyzed according to the addition of amine. Then, the wear rate calculated in two different amines was compared at the steam cycle in NPPs. As a result, increasing the pH at operating temperature (Hot pH) can reduce the rate of FAC damage significantly. Wall-thinning is affected by amine characteristics depending on temperature and quality of water.

  16. Effects of herbicides and freshwater discharge on water chemistry, toxicity and benthos in a Uruguayan sandy beach.

    Science.gov (United States)

    Sauco, Sebastián; Eguren, Gabriela; Heinzen, Horacio; Defeo, Omar

    2010-01-01

    Environmental water chemistry analysis and microcosm toxicity bioassays (MTB) were performed to assess lethality of herbicides on the mole crab Emerita brasiliensis in a sandy beach affected by a freshwater discharge (Andreoni canal) from rice crops. A 5-yr macrocosm field sampling (MFS) was conducted to evaluate freshwater effects on population abundance. Propanil was only detected at the inner portion of the Andreoni canal (IAC), whereas quinclorac and clomazone were found at the IAC and at the canal mouth (CM). A major propanil metabolite was detected at the CM. Herbicides were undetectable at 13km from the CM. MTB showed an increased susceptibility to propanil with decreasing crab sizes. The MFS showed a drastic decrease in abundance towards the freshwater discharge, concurrently with decreasing salinities. The triad approach that included water analyses, toxicological experiments and long-term field sampling allowed rejecting relationships between herbicide exposure and mole crab lethal effects.

  17. Interactions between groundwater and surface water in a Virginia coastal plain watershed. 2. Acid-base chemistry

    Science.gov (United States)

    O'Brien, A. K.; Eshleman, K.N.; Pollard, J.S.

    1994-01-01

    At the Reedy Creek watershed sulphate concentrations were higher and alkalinity lower in the groundwater in the hillslope than in the stream. Sulphate concentrations and alkalinity observed in groundwater in the wetland were usually between those of the hillslope and stream. These data suggest that the wetland is a sink for sulphate and acidity; sulphate reduction may be an important mechanism for generating alkalinity in the wetland. The DOC concentrations were higher in the stream and wetland groundwater than in hillslope groundwater. No consistent spatial patterns in sulphate concentrations were observed in surface water chemistry under base flow conditions. Stream discharge was found to be positively correlated with base flow sulphate concentrations and inversely correlated with alkalinity. A sulphate mass balance indicated that approximately 30% of the estimated 24.9 kg SO42-/ha yr wet atmospheric input was exported from the watershed as sulphate in stream runoff in the water year 1990. -from Authors

  18. Mine-water chemistry: the good, the bad and the ugly

    Energy Technology Data Exchange (ETDEWEB)

    Banks, B.; Banks, S.B. [Norges Geologiske Undersoekelse, Trondheim (Norway); Younger, P.L. [Newcastle Univ. (United Kingdom). Dept. of Civil Engineering; Arnesen, R.T.; Iversen, E.R. [Norwegian Inst. for Water Research (NIVA), Oslo (Norway)

    1997-10-01

    Contaminative mine drainage waters have become one of the major hydrogeological and geochemical problems arising from mankind`s intrusion into the geosphere. Mine drainage waters in Scandinavia and the United Kingdom are of three main types: (1) saline formation waters; (2) acidic, heavy-metal-containing, sulphate waters derived from pyrite oxidation, and (3) alkaline, hydrogen-sulphide-containing, heavy-metal-poor waters resulting from buffering reactions and/or sulphate reduction. Mine waters are not merely to be perceived as problems, they can be regarded as industrial or drinking water sources and have been used for sewage treatment, tanning and industrial metals extraction. Mine-water problems may be addressed by isolating the contaminant source, by suppressing the reactions releasing contaminants, or by active or passive water treatment. Innovative treatment techniques such as galvanic suppression, application of bactericides, neutralising or reducing agents (pulverised fly ash-based grouts, cattle manure, whey, brewers` yeast) require further research. (orig.)

  19. Effect of resuspension on the release of heavy metals and water chemistry in anoxic and oxic sediments

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, Kyung-Yup; Kim, Hong-Seok; Hwang, Inseong [School of Civil and Environmental Engineering, Pusan National University, Busan (Korea, Republic of)

    2011-10-15

    Two types of river sediments with contrasting characteristics (anoxic or oxic) were resuspended and the release of heavy metals and changes in water chemistry were investigated. During resuspension of the anoxic sediment, the dissolved oxygen (DO) concentration and redox potential of the water layer decreased abruptly within the first 1 min, followed by increases toward the end of the resuspension period. Heavy metals were released rapidly in the first 6 h, probably due to the oxidation of acid volatile sulfide (AVS) of the anoxic sediment, and then the aqueous phase concentrations of the heavy metals decreased due to resorption onto the sediment until the 12-h point. During resuspension of the oxic sediment, the DO concentration and redox potential remained relatively constant in the oxic ranges. The heavy metals were released from the oxic sediment gradually during a 24-h resuspension period. The temporal maximum concentrations of Ni, Cu, Zn, and Cd in the aqueous phases in both experiments frequently exceeded the USEPA water quality criteria or the water quality guidelines of Australia and New Zealand. This suggests that a resuspension event could bring about temporal water quality deterioration in the two sediment environments. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  20. Aespoe Hard Rock Laboratory. Prototype repository. Analyses of microorganisms, gases, and water chemistry in buffer and backfill, 2010

    Energy Technology Data Exchange (ETDEWEB)

    Lydmark, Sara [Microbial Analytics Sweden AB, Moelnlycke (Sweden)

    2011-06-15

    The prototype repository (hereafter, 'Prototype') is an international project to build and study a fullscale model of the planned Swedish final repository for spent nuclear fuel. However, the Prototype differs from a real storage in that it is drained, which makes the swelling pressure lower in the Prototype than in a real storage facility. The heat from the radioactive decay is simulated by electrical heaters. The project is being conducted at the Aespoe Hard Rock Laboratory (HRL) in crystalline rock at a depth of approximately 450 m. A monitoring programme is investigating the evolution of the water chemistry, gas, and microbial activity at the site, and a specific aim is to monitor the microbial consumption of oxygen in situ in the Prototype. This document describes the results of the analyses of microbes, gases, and chemistry inside the Prototype in 2010. Hydrogen, helium, nitrogen, oxygen, carbon monoxide, carbon dioxide, methane, ethane, and ethene were analysed at the following sampling points in the Prototype: KBU10001, KBU10002, KBU10004, KBU10008, and KFA04. Where the sampling points in the Prototype delivered pore water, the water was analysed for amount of ATP (i.e. the biovolume), culturable heterotrophic aerobic bacteria (CHAB), sulphate-reducing bacteria (SRB), methane-oxidizing bacteria (MOB), and iron-reducing bacteria (IRB). The pore water collected from the Prototype was subject to as many chemical analyses as the amount of water allowed. Chemical analyses were also performed on pore water from two additional sampling points, KBU10005 and KBU10006. Chemical data from a previous investigation of the groundwater outside the Prototype were compared with the pore water chemistry. The improved sampling and analysis protocols introduced in 2007 worked very well. The International Progress Report (IPR) 08-01 (Eriksson 2008) revealed that many of the hydrochemical sampling points differ greatly from each other. The 16 sampling points were

  1. Research in physical chemistry and chemical education: Part A: Water Mediated Chemistry of Oxidized Atmospheric Compounds Part B: The Development of Surveying Tools to Determine How Effective Laboratory Experiments Contribute to Student Conceptual Understanding

    Science.gov (United States)

    Maron, Marta Katarzyna

    This dissertation is a combination of two research areas, experimental physical chemistry, Chapters I to V, and chemical education, Chapters VI to VII. Chapters I to V describe research on the water-mediated chemistry of oxidized atmospheric molecules and the impact that water has on the spectra of these environmental systems. The role of water in the Earth's atmosphere has been of considerable interest due to its ability to impact chemistry and climate. Oxidized atmospheric molecules in the presence of water have the ability to form hydrogen bonded water complexes. The spectroscopic investigation of nitric acid-water complexes, outlined in Chapter III, was undertaken to characterize intermolecular hydrogen bonds in a water-restricted environment at ambient temperatures. Additionally, this characterization of nitric acid-water complexes allowed for the comparison of calculated overtone OH-stretching vibrational band frequencies, intensities, and anharmonicities of intermolecular hydrogen-bonded water complexes with experimental observations. Oxidized organic molecules, such as aldehydes and ketones, in addition to forming hydrogen-bonded water complexes can undergo a hydration reaction of the carbonyl group and form germinal diols in the presence of water. This chemistry has been studied extensively in bulk aqueous media, however little is known about this process in the gas-phase at low water concentrations. The focus of the studies outlined in Chapters IV and V is motivated by the ability of pyruvic acid and formaldehyde to form germinal diols and water complexes in water-restricted environment. This water-mediated chemistry changes the physical and chemical properties of these organic molecules, therefore, impacting the partitioning between gas and particle phase, as well as the chemistry and photochemistry of oxidized organic molecules in the Earth's atmosphere. The results presented in this dissertation may help resolve the significant discrepancy between

  2. Geologic, water-chemistry, and hydrologic data from multiple-well monitoring sites and selected water-supply wells in the Santa Clara Valley, California, 1999-2003

    Science.gov (United States)

    Newhouse, M.W.; Hanson, R.T.; Wentworth, C.M.; Everett, Rhett; Williams, C.F.; Tinsley, J.C.; Noce, T.E.; Carkin, B.A.

    2004-01-01

    To better identify the three-dimensional geohydrologic framework of the Santa Clara Valley, lithologic, geologic, geophysical, geomechanical, hydraulic, and water-chemistry data were collected from eight ground-water multiple-well monitoring sites constructed in Santa Clara County, California, as part of a series of cooperative studies between the U.S. Geological Survey and the Santa Clara Valley Water District. The data are being used to update and improve the three-dimensional geohydrologic framework of the basin and to address issues related to water supply, water chemistry, sequence stratigraphy, geology, and geological hazards. This report represents a compilation of data collected from 1999 to 2003, including location and design of the monitoring sites, cone penetrometer borings, geologic logs, lithologic logs, geophysical logs, core analysis, water-chemistry analysis, ground-water-level measurements, and hydraulic and geomechanical properties from wells and core samples. Exploratory cone penetrometer borings taken in the upper 17 to 130 feet at six of the monitoring sites identified the base of Holocene as no deeper than 75 feet in the central confined area and no deeper than 35 feet in the southern unconfined areas of the valley. Generalized lithologic characterization from the monitoring sites indicates about four to six different aquifer units separated by relatively fine-grained units occur within the alluvial deposits shallower than 860 feet deep. Analysis of geophysical logs indicates that coarse-grained units varied in thickness between 10 and 25 feet in the southeastern unconfined area of the valley and between 50 and 200 feet in the south-central and southwestern areas of the valley. Deviations from temperature-gradient logs indicate that the majority of horizontal ground-water flow occurs above a depth of 775 feet in the south central and above 510 feet in the southeastern areas of the valley. Bulk physical properties from more than 1,150 feet of

  3. Influence of water chemistry on the acute toxicity of copper and zinc to the cladoceran Ceriodaphnia cf dubia.

    Science.gov (United States)

    Hyne, Ross V; Pablo, Fleur; Julli, Moreno; Markich, Scott J

    2005-07-01

    This study determined the influence of key water chemistry parameters (pH, alkalinity, dissolved organic carbon [DOC], and hardness) on the aqueous speciation of copper and zinc and its relationship to the acute toxicity of these metals to the cladoceran Ceriodaphnia cf dubia. Immobilization tests were performed for 48-h in synthetic or natural waters buffered at various pH values from 5.5 to 8.4 (other chemical parameters held constant). The toxicity of copper to C. cf dubia decreased fivefold with increasing pH, whereas the toxicity of zinc increased fivefold with increasing pH. The effect of DOC on copper and zinc toxicity to C. cf dubia was determined using natural fulvic acid in the synthetic water. Increasing DOC was found to decrease linearly the toxicity of copper, with the mean effect concentration of copper that immobilized 50% of the cladocerans (EC50) value 45 times higher at 10 mg/L, relative to 0.1 mg/L DOC at pH 6.5. In contrast, the addition of 10 mg/L DOC only resulted in a very small (1.3-fold) reduction in the toxicity of zinc to C. cf dubia. Copper toxicity to C. cf dubia generally did not vary as a function of hardness, whereas zinc toxicity was reduced by a factor of only two, with an increase in water hardness from 44 to 374 mg CaCO3/L. Increasing bicarbonate alkalinity of synthetic waters (30-125 mg/L as CaCO3) decreased the toxicity of copper up to fivefold, which mainly could be attributed to the formation of copper-carbonate complexes, in addition to a pH effect. The toxicity of copper added to a range of natural waters with varying DOC content, pH, and hardness was consistent with the toxicity predicted using the data obtained from the synthetic waters.

  4. The influence of EI-21 redox ion-exchange resins on the secondary-coolant circuit water chemistry of vehicular nuclear power installations

    Science.gov (United States)

    Moskvin, L. N.; Rakov, V. T.

    2015-06-01

    The results obtained from testing the secondary-coolant circuit water chemistry of full-scale land-based prototype bench models of vehicular nuclear power installations equipped with water-cooled water-moderated and liquid-metal reactor plants are presented. The influence of copper-containing redox ionexchange resins intended for chemically deoxygenating steam condensate on the working fluid circulation loop's water chemistry is determined. The influence of redox ion-exchange resins on the water chemistry is evaluated by generalizing an array of data obtained in the course of extended monitoring using the methods relating to physicochemical analysis of the quality of condensate-feedwater path media and the methods relating to metallographic analysis of the state of a faulty steam generator's tube system surfaces. The deoxygenating effectiveness of the normal state turbine condensate vacuum deaeration system is experimentally determined. The refusal from applying redox ion-exchange resins in the condensate polishing ion-exchange filters is formulated based on the obtained data on the adverse effect of copper-containing redox ionexchange resins on the condensate-feedwater path water chemistry and based on the data testifying a sufficient effect from using the normal state turbine condensate vacuum deaeration system. Data on long-term operation of the prototype bench model of a vehicular nuclear power installation without subjecting the turbine condensate to chemical deoxygenation are presented.

  5. Variability in the chemistry of private drinking water supplies and the impact of domestic treatment systems on water quality.

    Science.gov (United States)

    Ander, E L; Watts, M J; Smedley, P L; Hamilton, E M; Close, R; Crabbe, H; Fletcher, T; Rimell, A; Studden, M; Leonardi, G

    2016-12-01

    Tap water from 497 properties using private water supplies, in an area of metalliferous and arsenic mineralisation (Cornwall, UK), was measured to assess the extent of compliance with chemical drinking water quality standards, and how this is influenced by householder water treatment decisions. The proportion of analyses exceeding water quality standards were high, with 65 % of tap water samples exceeding one or more chemical standards. The highest exceedances for health-based standards were nitrate (11 %) and arsenic (5 %). Arsenic had a maximum observed concentration of 440 µg/L. Exceedances were also high for pH (47 %), manganese (12 %) and aluminium (7 %), for which standards are set primarily on aesthetic grounds. However, the highest observed concentrations of manganese and aluminium also exceeded relevant health-based guidelines. Significant reductions in concentrations of aluminium, cadmium, copper, lead and/or nickel were found in tap waters where households were successfully treating low-pH groundwaters, and similar adventitious results were found for arsenic and nickel where treatment was installed for iron and/or manganese removal, and successful treatment specifically to decrease tap water arsenic concentrations was observed at two properties where it was installed. However, 31 % of samples where pH treatment was reported had pH water regulations), suggesting widespread problems with system maintenance. Other examples of ineffectual treatment are seen in failed responses post-treatment, including for nitrate. This demonstrates that even where the tap waters are considered to be treated, they may still fail one or more drinking water quality standards. We find that the degree of drinking water standard exceedances warrant further work to understand environmental controls and the location of high concentrations. We also found that residents were more willing to accept drinking water with high metal (iron and manganese) concentrations than

  6. Comparison of surface water chemistry and weathering effects of two lake basins in the Changtang Nature Reserve, China.

    Science.gov (United States)

    Wang, Rui; Liu, Zhaofei; Jiang, Liguang; Yao, Zhijun; Wang, Junbo; Ju, Jianting

    2016-03-01

    The geochemistry of natural waters in the Changtang Nature Reserve, northern Tibet, can help us understand the geology of catchments, and provide additional insight in surface processes that influence water chemistry such as rock weathering on the Qinghai-Tibet Plateau. However, severe natural conditions are responsible for a lack of scientific data for this area. This study represents the first investigation of the chemical composition of surface waters and weathering effects in two lake basins in the reserve (Lake Dogaicoring Qiangco and Lake Longwei Co). The results indicate that total dissolved solids (TDS) in the two lakes are significantly higher than in other gauged lakes on the Qinghai-Tibet Plateau, reaching 20-40g/L, and that TDS of the tectonic lake (Lake Dogaicoring Qiangco) is significantly higher than that of the barrier lake (Lake Longwei Co). Na(+) and Cl(-) are the dominant ions in the lake waters as well as in the glacier-fed lake inflows, with chemical compositions mainly affected by halite weathering. In contrast, ion contents of inflowing rivers fed by nearby runoff are lower and concentrations of dominant ions are not significant. Evaporite, silicate, and carbonate weathering has relatively equal effects on these rivers. Due to their limited scope, small streams near the lakes are less affected by carbonate than by silicate weathering.

  7. Spatial and temporal analysis of water chemistry records (1958-2000) in the Huanghe (Yellow River) basin

    Science.gov (United States)

    Chen, Jingsheng; Wang, Feiyue; Meybeck, Michel; He, Dawei; Xia, Xinghui; Zhang, Litian

    2005-09-01

    The chemistry of major dissolved ions (Ca2+, Mg2+, Na+ + K+, HCO3-, SO42-, Cl-) and dissolved silica (SiO2) in the river water of the Huanghe (Yellow River), China, was studied from historical records at 100 stations in the drainage basin for the period 1958-2000 (not all the parameters were continuously monitored during the entire period). This river system (750,000 km2) presents an exceptional temporal and spatial water chemistry variability compared to other major rivers. The total dissolved solid (TDS) concentration of the Huanghe varied over 2 to 3 orders of magnitude throughout the basin, with a median TDS concentration of 452 mg/L, which is about 4 times the world spatial median value (WSM). In particular, the concentrations of Na+ + K+, SO42-, and Cl- were 10-20 times higher than in other major world rivers. Similar to the Changjiang (Yangtze River) and many other Himalayan rivers, the TDS at a given station is seasonally variable and inversely related to river runoff with a variation factor less than 2.0, despite a water dilution of fourfold to fivefold in the summer flood season. In addition to chemical weathering of sedimentary rocks, evaporation and fractional crystallization were found to be the major natural process controlling the major element chemistry of the Huanghe, owing to the abundance of loess and clastic rocks under arid and semiarid climates. A persistent increasing trend from year to year has been observed in the concentrations of TDS and all the salts except for HCO3- at all main-channel stations except for the uppermost Lanzhou. The rate of increase in the TDS concentration was the highest in the middle reaches (10.52 mg/L yr-1 at Toudaoguai) and remained to be unusually high in the lower reaches (5.5 mg/L yr-1 at Stations Luokou and Lijin). The increasing trend coincided with a significant decrease in water discharge at most of the main-channel stations in the past 40 years, and is attributed to increasing regulations of reservoirs and

  8. Synthesis of a Two-Dimensional Covalent Organic Monolayer through Dynamic Imine Chemistry at the Air/Water Interface.

    Science.gov (United States)

    Dai, Wenyang; Shao, Feng; Szczerbiński, Jacek; McCaffrey, Ryan; Zenobi, Renato; Jin, Yinghua; Schlüter, A Dieter; Zhang, Wei

    2016-01-01

    A two-dimensional covalent organic monolayer was synthesized from simple aromatic triamine and dialdehyde building blocks by dynamic imine chemistry at the air/water interface (Langmuir-Blodgett method). The obtained monolayer was characterized by optical microscopy, scanning electron microscopy, and atomic force microscopy, which unambiguously confirmed the formation of a large (millimeter range), unimolecularly thin aromatic polyimine sheet. The imine-linked chemical structure of the obtained monolayer was characterized by tip-enhanced Raman spectroscopy, and the peak assignment was supported by spectra simulated by density functional theory. Given the modular nature and broad substrate scope of imine formation, the work reported herein opens up many new possibilities for the synthesis of customizable 2D polymers and systematic studies of their structure-property relationships.

  9. Characterization of Passive Film Formed on 304 SS in Simu-lated Alkaline Water Chemistries Containing Sulfur at 300℃

    Institute of Scientific and Technical Information of China (English)

    夏大海; 孙毅飞; 范洪强

    2015-01-01

    Passivity degradation of 304 stainless steel(SS) in simulated alkaline water chemistries at 300,℃was investigated using polarization curve, scanning electron microscope, time-of-flight secondary ion mass spectrome-try(SIMS) and X-ray photoelectron spectroscopy(XPS). Experimental results indicated that 304,SS was self-passive in the test solution and the thickness of passive film was about 500 nm. Hydroxide was enriched in the outer layer whereas oxide was enriched in the inner layer. Sulfur in thiosulfate could be reduced into lower valence of sulfur and enter the passive film so that the composition of passive film was modified by sulfur. Fe and Cr were enriched in the passive film whereas Ni was depleted in the passive film.

  10. One year water chemistry monitoring of the flooding of the Meirama open pit (NW Spain)

    Science.gov (United States)

    Delgado, J.; Juncosa, R.; Vázquez, A.; Fernández-Bogo, S.

    2009-04-01

    In December, 2007, after 30 years of operations, the mine of Meirama finished the extraction of brown lignite. Starting in April 2008, the flooding of the open pit has started and this is leading to the formation of a large mining lake (~2 km2 surface and up to 180 m depth) in which surface (river and rain water) and ground waters are involved. Since the beginning of the flooding, lake waters are weekly sampled and analyzed for temperature, pH, redox, EC, TDS, TSS, DO,DIC, DOC, turbidity, alkalinity/acidity as well as nearly 40 inorganic chemical components. Stable water isotopes (deuterium and oxygen) are also being recorded. In order to better understand the dynamic chemical evolution of lake waters, the chemical characteristics of rain water as well as a series of lake tributaries and ground waters are also being measured. Since the beginning of the flooding process, the chemical quality of lake water has experienced an interesting evolution that obeys to a variety of circumstances. The silicic geologic substratum of the catchment determines that both ground and surface waters have a rather low alkalinity. Moreover, the presence of disseminated sulfides (mainly pyrite) within the schistous materials of the mine slopes and internal rock dumps provokes a significant acidic load. From April to October 2008, the lake waters had only the contribution of rain and ground waters. Since the beginning of October, a significant volume of surface waters has been derived to the mine hole. Taking pH as indicator, the first water body had a rather acidic pH (~3) which was progressively amended with the addition of a certain amount of lime to reach an upper value of ~8 by late August. The diminution in the addition of lime up to its elimination, in December, has conducted to the progressive acidification of the lake. At present, an instrumented floating deck is being deployed in the lake. This device will serve as a base point where it is planned to locate a series of

  11. Mukilteo water sensor time series - Field work coupling measurements of carbon chemistry and distribution of free-living organisms

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — To estimate the carbon chemistry conditions experienced by free-living organisms, we will conduct coupled biological/carbon chemistry sampling for key zooplankton...

  12. Thermal chemistry of hydrazine on clean and oxygen- and water-predosed Cu(110) single-crystal surfaces

    Science.gov (United States)

    Yao, Yunxi; Zaera, Francisco

    2016-08-01

    The chemistry of hydrazine on Cu(110) single-crystal surfaces was probed under ultrahigh vacuum (UHV) conditions by temperature-programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS). Survey TPD experiments identified molecular nitrogen and ammonia as the main desorbing products from thermal activation of the adsorbate, but small amounts of diazene and NH2· radicals were also detected. At saturation coverage, N2 production leads NH3 desorption by approximately 10 K (with TPD peaks at 350 K versus 360 K, respectively), indicating a preference for dehydrogenation over N-N bond scission steps, and additional nitrogen was seen at even lower temperatures (320 K) in experiments starting with even higher doses of hydrazine. On the other hand, the formation of NH3 and NH2·, which desorb in a wide range of temperatures between approximately 300 K and 700 K, dominates in experiments with low N2H4 doses, presumably because a stronger interaction of the N-N bond with the metal in the flat adsorption geometry expected at such low coverages. Dosing at room temperature seems to also facilitate the dissociative adsorption, albeit via dehydrogenation steps that lead to the subsequent production of more significant amounts of diazene and of molecular hydrogen (in addition to N2, NH3, and NH2·). Preadsorption of oxygen on the Cu(110) surface helps stabilize the hydrazine, increasing its desorption temperature and helping with the low-temperature (320 K) production of N2. Coadsorption of hydrazine with water leads to facile proton exchange, as indicated by the production of NH2D in TPD experiments with N2H4 + D2O. This isotope scrambling must occur at cryogenic temperatures because all water desorbs from the surface below 200 K and no other changes in surface chemistry are observed after that. The implications of all this chemistry to practical applications that may use hydrazine in surface reactions with copper, including its use as a reducing agent in atomic layer

  13. Trends and seasonality in stream water chemistry in two moorland catchments of the Upper River Wye, Plynlimon

    Directory of Open Access Journals (Sweden)

    B. Reynolds

    1997-01-01

    Full Text Available Stream water chemistry in the Cyff and Gwy subcatchments within the headwaters of the River Wye has been monitored regularly since 1980. In the Gwy, which is a predominantly semi-natural grassland catchment, land use has remained relatively static over the monitoring period, whilst the Cyff catchment is more buffered because of base cation inputs from agricultural improvement and ground water sources. Using a variety of statistical techniques, the long-term data are examined for evidence of trends after eliminating seasonal effects. The results highlight some of the difficulties associated with the analysis of longterm water quality data which show considerable variability over a variety of timescales. Some of this variability can be explained in terms of hydrochemical responses to climatic extremes and episodic events such as large atmospheric inputs of seasalts. The long-term fluctuations in solute concentration underline the continuing need for maintaining consistent long-term monitoring at sensitive upland sites if underlying trends related to gradual changes in pollutant deposition or climate are to be detected with any certainty.

  14. Removal of graphene oxide nanomaterials from aqueous media via coagulation: Effects of water chemistry and natural organic matter.

    Science.gov (United States)

    Duan, Lin; Hao, Rongjie; Xu, Zhu; He, Xizhen; Adeleye, Adeyemi S; Li, Yao

    2017-02-01

    With the increasing use of graphene oxide (GO) nanomaterials, its possible environmental release and human effects have received much attention. As GO may enter drinking or wastewater treatment systems like other carbonaceous nanomaterials, and have potential impact on human and/or environmental health, its removal efficiency during water treatment is important and requires investigation. In this study, the removal efficiency of GO during water treatment procedure via coagulation was evaluated, and the effects of solution chemistry and natural organic matter on the coagulation-based removal of GO nanomaterials were investigated. The results indicate that the removal efficiency of GO with alum coagulation can reach 80% with 20 mg/L alum dosage at neutral pH, and will not change significantly with higher concentration of alum. The coagulation mechanism and efficiency were strongly affected by the Al species in aqueous phase, which are controlled by pH. Co-existing cations (e.g. Na) may have minimal effect on GO removal efficiency, and the presence of humic acid (HA) suppresses coagulation remarkably at alum concentrations below 40 mg/L. The results from this study provide critical information for predicting the removal efficiency of GO nanomaterials during alum coagulation phase of water treatment procedure.

  15. Phosphorus in Cold-Water Corals as a Proxy for Seawater Nutrient Chemistry

    Science.gov (United States)

    Montagna, Paolo; McCulloch, Malcolm; Taviani, Marco; Mazzoli, Claudio; Vendrell, Begoña

    2006-06-01

    Phosphorus is a key macronutrient being strongly enriched in the deep ocean as a result of continuous export and remineralization of biomass from primary production. We show that phosphorus incorporated within the skeletons of the cosmopolitan cold-water coral Desmophyllum dianthus is directly proportional to the ambient seawater phosphorus concentration and thus may serve as a paleo-oceanographic proxy for variations in ocean productivity as well as changes in the residence times and sources of deep-water masses. The application of this tool to fossil specimens from the Mediterranean reveals phosphorus-enriched bottom waters at the end of the Younger Dryas period.

  16. Theoretical investigations of metallic surfaces for water chemistry; Theoretische Untersuchungen metallischer Oberflaechen fuer die Wasserstoffchemie

    Energy Technology Data Exchange (ETDEWEB)

    Schnur, Sebastian

    2010-11-19

    Properties of the metal-water interface have been addressed by periodic density functional theory calculations, in particular with respect to the electronic and geometric structures of water bilayers on several transition metal surfaces. The structure and the vibrational spectra of water bilayers at room temperatures have been studied performing ab initio molecular dynamics simulations. In order to model varying electrode potentials, an explicite counter electrode has been implemented in a periodic density functional theory code, and first preliminary results using this implementation will be presented. (orig.)

  17. The chemistry and isotopic composition of waters in the low-enthalpy geothermal system of Cimino-Vico Volcanic District, Italy

    Science.gov (United States)

    Battistel, Maria; Hurwitz, Shaul; Evans, William C.; Barbieri, Maurizio

    2016-12-01

    Geothermal energy exploration is based in part on interpretation of the chemistry, temperature, and discharge rate of thermal springs. Here we present the major element chemistry and the δD, δ18O, 87Sr/86Sr and δ11B isotopic ratio of groundwater from the low-enthalpy geothermal system near the city of Viterbo in the Cimino-Vico volcanic district of west-Central Italy. The geothermal system hosts many thermal springs and gas vents, but the resource is still unexploited. Water chemistry is controlled by mixing between low salinity,HCO3-rich fresh waters (extraction of boron but also promotes conductive cooling, partially masking the heat present in the reservoir. Overall data from this study is consistent with previous studies that concluded that the geothermal system has a large energy potential.

  18. Willapa NWR: Initial Survey Instructions for Tidal Restoration Monitoring - Water Chemistry

    Data.gov (United States)

    US Fish and Wildlife Service, Department of the Interior — Through an active role in local, state, and federal partnerships, the refuge staff works to maintain the ecological integrity and water quality of the Willapa Bay...

  19. Chemistry, Toxicity and Health Risk Assessment of Drinking Water Disinfection ByProducts

    Science.gov (United States)

    Disinfection byproducts (DBPs) are formed by the reaction of oxidizing chemicals (such as chlorine, ozone and chloramines) used to control waterborne pathogens with natural organic material and other substances in water. DBP mixture composition varies as a function of geographic ...

  20. Spatiotemporal assessment of water chemistry in intermittently open/closed coastal lakes of Southern Baltic

    Science.gov (United States)

    Astel, Aleksander M.; Bigus, Katarzyna; Obolewski, Krystian; Glińska-Lewczuk, Katarzyna

    2016-12-01

    Ionic profile, pH, electrolytic conductivity, chemical oxygen demand and concentration of selected heavy metals (Ni, Cu, Zn, Fe and Mn) were determined in water of 11 intermittently closed and open lakes and lagoons (ICOLLs) located in Polish coastline. Multidimensional data set was explored by the use of the self-organizing map (SOM) technique to avoid supervised and predictable division for fully isolated, partially and fully connected lakes. Water quality assessment based on single parameter's mean value allowed classification of majority of lakes to first or second class of purity according to regulation presenting classification approach applicable to uniform parts of surface waters. The SOM-based grouping revealed seven clusters comprising water samples of similar physico-chemical profile. Fully connected lakes were characterized by the highest concentration of components characteristic for sea salts (NaCl, MgCl2, MgSO4, CaSO4, K2SO4 and MgBr2), however spring samples from Łebsko were shifted to another cluster suggesting that intensive surface run-off and fresh-water inflow through Łupawa river decreases an impact of sea water intrusions. Forecasted characteristic of water collected in Resko Przymorskie lake was disturbed by high contamination by nitrites indicating accidental and local contamination due to usage of sodium nitrite for the curing of meat. Some unexpected sources of contamination was discovered in intermittently open and closed lakes. Presumably Zn contamination is due to use of wood preservatives to protect small wooden playgrounds or camping places spread around one of the lake, while increased concentration of Ni could be connected with grass and vegetation burning. Waters of Jamno lake are under the strongest anthropogenic impact due to inefficient removal of phosphates by waste water treatment plant and contamination by Fe and Mn caused by backwashing of absorption filters. Generally, the quality of ICOLLs' water was diversified, while

  1. Environmental Characteristics of Groundwater: an Application of PCA to Water Chemistry Analysis in Yulin

    Institute of Scientific and Technical Information of China (English)

    DONG Dong-lin; HUANG Song-lin; WU Qiang; ZHANG Rui; SONG Ying-xia; CHEN Shu-ke; LI Pei; LIU Shou-qiang; BI Cen-cen; LV Zhen-qi

    2007-01-01

    For our investigation into the water quality in Yulin city, we collected 76 typical water samples to be tested for particle quality. By applying a Romani type classification method the groundwater of Yulin city was classified into nine categories by type, i.e., Ca-HCO3, Na-HCO3, Na-HCO3-SO4-Cl, Na-HCO3-SO4, Na-Cl, Na-Cl-HCO3, Na-CaHCO3, Ca-Cl-HCO3 and Ca-HCO3-SO4-Cl. A principal component analysis was carried out in order to analyze the groundwater environment. From this analysis we considered that the information collected could be represented by 21 indices from which we extracted seven principal components, which, respectively, accounted for 37.4%, 13.0%, 8.1%,7.2%, 6.3%, 5.9% and 4.6% of the total variation. The results show that the groundwater environment of this region is largely determined by characteristic components of the natural groundwater background. One part of the water was polluted by leaching/eluviation of solid waste generated from coal mining. Another part of the ground water was contaminated by acid mine water from the coal layer and from improper irrigation. In addition, geological and hydrogeological conditions also cause changes in the water environment.

  2. Identifying biotic integrity and water chemistry relations in nonwadeable rivers of Wisconsin: Toward the development of nutrient criteria

    Science.gov (United States)

    Weigel, B.M.; Robertson, D.M.

    2007-01-01

    We sampled 41 sites on 34 nonwadeable rivers that represent the types of rivers in Wisconsin, and the kinds and intensities of nutrient and other anthropogenic stressors upon each river type. Sites covered much of United States Environmental Protection Agency national nutrient ecoregions VII-Mostly Glaciated Dairy Region, and VIII-Nutrient Poor, Largely Glaciated upper Midwest. Fish, macroinvertebrates, and three categories of environmental variables including nutrients, other water chemistry, and watershed features were collected using standard protocols. We summarized fish assemblages by index of biotic integrity (IBI) and its 10 component measures, and macroinvertebrates by 2 organic pollution tolerance and 12 proportional richness measures. All biotic and environmental variables represented a wide range of conditions, with biotic measures ranging from poor to excellent status, despite nutrient concentrations being consistently higher than reference concentrations reported for the regions. Regression tree analyses of nutrients on a suite of biotic measures identified breakpoints in total phosphorus (~0.06 mg/l) and total nitrogen (~0.64 mg/l) concentrations at which biotic assemblages were consistently impaired. Redundancy analyses (RDA) were used to identify the most important variables within each of the three environmental variable categories, which were then used to determine the relative influence of each variable category on the biota. Nutrient measures, suspended chlorophyll a, water clarity, and watershed land cover type (forest or row-crop agriculture) were the most important variables and they explained significant amounts of variation within the macroinvertebrate (R 2 = 60.6%) and fish (R 2 = 43.6%) assemblages. The environmental variables selected in the macroinvertebrate model were correlated to such an extent that partial RDA analyses could not attribute variation explained to individual environmental categories, assigning 89% of the explained

  3. Aespoe Hard Rock Laboratory. Prototype repository. Analyses of microorganisms, gases, and water chemistry in buffer and backfill, 2010

    Energy Technology Data Exchange (ETDEWEB)

    Lydmark, Sara [Microbial Analytics Sweden AB, Moelnlycke (Sweden)

    2011-06-15

    The prototype repository (hereafter, 'Prototype') is an international project to build and study a fullscale model of the planned Swedish final repository for spent nuclear fuel. However, the Prototype differs from a real storage in that it is drained, which makes the swelling pressure lower in the Prototype than in a real storage facility. The heat from the radioactive decay is simulated by electrical heaters. The project is being conducted at the Aespoe Hard Rock Laboratory (HRL) in crystalline rock at a depth of approximately 450 m. A monitoring programme is investigating the evolution of the water chemistry, gas, and microbial activity at the site, and a specific aim is to monitor the microbial consumption of oxygen in situ in the Prototype. This document describes the results of the analyses of microbes, gases, and chemistry inside the Prototype in 2010. Hydrogen, helium, nitrogen, oxygen, carbon monoxide, carbon dioxide, methane, ethane, and ethene were analysed at the following sampling points in the Prototype: KBU10001, KBU10002, KBU10004, KBU10008, and KFA04. Where the sampling points in the Prototype delivered pore water, the water was analysed for amount of ATP (i.e. the biovolume), culturable heterotrophic aerobic bacteria (CHAB), sulphate-reducing bacteria (SRB), methane-oxidizing bacteria (MOB), and iron-reducing bacteria (IRB). The pore water collected from the Prototype was subject to as many chemical analyses as the amount of water allowed. Chemical analyses were also performed on pore water from two additional sampling points, KBU10005 and KBU10006. Chemical data from a previous investigation of the groundwater outside the Prototype were compared with the pore water chemistry. The improved sampling and analysis protocols introduced in 2007 worked very well. The International Progress Report (IPR) 08-01 (Eriksson 2008) revealed that many of the hydrochemical sampling points differ greatly from each other. The 16 sampling points were

  4. Water-chemistry data collected in and near Kaloko-Honokohau National Historical Park, Hawaii, 2012–2014

    Science.gov (United States)

    Tillman, Fred D; Oki, Delwyn S.; Johnson, Adam G.

    2014-01-01

    Kaloko-Honokōhau National Historical Park (KAHO) on western Hawaiʻi was established in 1978 to preserve, interpret, and perpetuate traditional Native Hawaiian culture and activities, including the preservation of a variety of culturally and ecologically significant water resources that are vital to this mission. KAHO water bodies provide habitat for 1 threatened, 11 endangered, and 3 candidate threatened or endangered species. These habitats are sustained by, and in the case of ʻAimakapā Fishpond and the anchialine pools, entirely dependent on, groundwater from the Keauhou aquifer system. Development of inland impounded groundwater in the Keauhou aquifer system may affect the coastal freshwater-lens system on which KAHO depends, if the inland impounded-groundwater and coastal freshwater-lens systems are hydrologically connected. This report documents water-chemistry results from a U.S. Geological Survey study that collected and analyzed water samples from 2012 to 2014 from 25 sites in and near KAHO to investigate potential geochemical indicators in water that might indicate the presence or absence of a hydrologic connection between the inland impounded-groundwater and coastal freshwater-lens systems in the area. Samples were collected under high-tide and low-tide conditions for KAHO sites, and in dry-season and wet-season conditions for all sites. Samples were collected from two ocean sites, two fishponds, three anchialine pools, and three monitoring wells within KAHO. Two additional nearshore wells were sampled on property adjacent to and north of KAHO. Additional samples from the freshwater-lens system were collected from six inland wells located upslope from KAHO, including three production wells. Seven production wells in the inland impounded-groundwater system also were sampled. Water samples were analyzed for major ions, selected trace elements, rare-earth elements, strontium-isotope ratio, and stable isotopes of water. Precipitation samples from five

  5. Monitoring of heavy metal load - by mosses or rain water chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Ruoho-Airola, T. [Finnish Meteorological Inst., Helsinki (Finland); Maekelae, K. [National Board of Waters and the Environment, Helsinki (Finland)

    1995-12-31

    The deposition of heavy metals is usually determined from precipitation chemistry but the moss technique has been increasingly used, particularly in the Nordic countries. Some international monitoring programmes, e.g. UN/ECE Integrated Monitoring, give them as alternative methods. However, their comparability has not been sufficiently determined. This study compares the two monitoring methods for Pb, Cd, Cu and Zn, which have different sources. The metal industry is an important source of Pb and Cd emissions. Long- range transport as well as traffic and local emissions are also important sources for Pb. The use of fertilizers and fossil fuels also result in Cd emissions. Cu and Zn are emitted from metal industries and local sources. Unlike Pb and Cd, Cu and Zn are essential elements for living organisms. Cu and Zn are needed in many enzymes and Zn in proteins. Mosses are thought to take all their nutrients from the air. The deposition of heavy metals is also effectively retained by mosses and may be used to indicate levels of heavy metal deposition. In northern countries the mosses are isolated from air (and therefore also from deposition) by snow in winter. In this study both the bulk deposition of the whole year (later `total deposition`) and the bulk deposition of the snow-free period (later `bare ground deposition`) are compared to the metal concentrations in mosses. (author)

  6. Surface chemistry of rare-earth oxide surfaces at ambient conditions: reactions with water and hydrocarbons

    Science.gov (United States)

    Külah, Elçin; Marot, Laurent; Steiner, Roland; Romanyuk, Andriy; Jung, Thomas A.; Wäckerlin, Aneliia; Meyer, Ernst

    2017-01-01

    Rare-earth (RE) oxide surfaces are of significant importance for catalysis and were recently reported to possess intrinsic hydrophobicity. The surface chemistry of these oxides in the low temperature regime, however, remains to a large extent unexplored. The reactions occurring at RE surfaces at room temperature (RT) in real air environment, in particular, in presence of polycyclic aromatic hydrocarbons (PAHs), were not addressed until now. Discovering these reactions would shed light onto intermediate steps occurring in automotive exhaust catalysts before reaching the final high operational temperature and full conversion of organics. Here we first address physical properties of the RE oxide, nitride and fluoride surfaces modified by exposure to ambient air and then we report a room temperature reaction between PAH and RE oxide surfaces, exemplified by tetracene (C18H12) on a Gd2O3. Our study evidences a novel effect – oxidation of higher hydrocarbons at significantly lower temperatures (~300 K) than previously reported (>500 K). The evolution of the surface chemical composition of RE compounds in ambient air is investigated and correlated with the surface wetting. Our surprising results reveal the complex behavior of RE surfaces and motivate follow-up studies of reactions between PAH and catalytic surfaces at the single molecule level. PMID:28327642

  7. Multivariate statistical analysis of surface water chemistry: A case study of Gharasoo River, Iran

    Directory of Open Access Journals (Sweden)

    MH Sayadi

    2014-09-01

    Full Text Available Regional water quality is a hot spot in the environmental sciences for inconsistency of pollutants. In this paper, the surface water quality of the Gharasoo River in western Iran is assessed incorporating multivariate statistical techniques. Parameters like EC, TDS, pH, HCO3-, Cl-, SO4 2-, Ca2+, Mg2+ and Na+ were analyzed. Principal component and factor analysis is showed the parameters generated 3 significant factors, which explained 73.06% of the variance in data sets. Factor 1 may be derived from agricultural activities and subsequent release of EC, TDS, SO4 2- and Na+ to the water. Factor 2 could be influenced by domestic pollution and explained the deliverance of HCO3-, Cl- and Mg2+ into the water. Factor 3 contains hydro-geochemical variable Ca2+ and pH, originating from mineralization of the geological components of bed sediments and soils of watershed area. Likewise, the clustering analysis generated 3 groups of the stations as the groups had similar characteristic features. Pearson correlation analysis showed significant correlations between HCO3- and Mg2+ (0.775, Ca2+ (0.552 as well as TDS and Na+ (0.726. With reference to multivariate statistical analyses it can be concluded that the agricultural, domestic and hydro-geochemical sources are releasing the pollutants into the Gharasoo River water.

  8. Field testing of lake water chemistry with a portable and an AUV-based mass spectrometer.

    Science.gov (United States)

    Hemond, Harry F; Mueller, Amy V; Hemond, Michael

    2008-10-01

    Two mass spectrometers (MS) are tested for the measurement of volatile substances, such as hydrocarbons and metabolic gases, in natural waters. KOALA is a backpackable MS operated from above the water surface, in which samples are pumped through a flow cell using a syringe. NEREUS is an underwater instrument hosted by an autonomous underwater vehicle (AUV) that is linked to a communications network to provide chemical data in real time. The mass analyzers of the two MS are nearly identical cycloids, and both use flat-plate membrane inlets. Testing took place in an eutrophic, thermally stratified lake exhibiting steep chemical gradients and significant levels of methane. KOALA provided rapid multispecies analysis of dissolved gases, with a detection limit for methane of 0.1 ppm (readily extendable to 0.01 ppm) and savings of time of at least a factor of 10 compared to that of conventional analysis. The AUV-mounted NEREUS additionally provided rapid spatial coverage and the capability of performing chemical surveys autonomously. Tests demonstrated the need for temperature control of a membrane inlet when steep thermal gradients are present in a water body, as well as the benefits of co-locating all sensors on the AUV to avoid interference from chemically different waters entering and draining from the free-flooding outer hull. The ability to measure dissolved volatiles provided by MS offers potential for complementarity with ionic sensors in the study of natural waters, such as in the case of the carbonate system.

  9. Water oxidation chemistry of a synthetic dinuclear ruthenium complex containing redox-active quinone ligands.

    Science.gov (United States)

    Isobe, Hiroshi; Tanaka, Koji; Shen, Jian-Ren; Yamaguchi, Kizashi

    2014-04-21

    We investigated theoretically the catalytic mechanism of electrochemical water oxidation in aqueous solution by a dinuclear ruthenium complex containing redox-active quinone ligands, [Ru2(X)(Y)(3,6-tBu2Q)2(btpyan)](m+) [X, Y = H2O, OH, O, O2; 3,6-tBu2Q = 3,6-di-tert-butyl-1,2-benzoquinone; btpyan =1,8-bis(2,2':6',2″-terpyrid-4'-yl)anthracene] (m = 2, 3, 4) (1). The reaction involves a series of electron and proton transfers to achieve redox leveling, with intervening chemical transformations in a mesh scheme, and the entire molecular structure and motion of the catalyst 1 work together to drive the catalytic cycle for water oxidation. Two substrate water molecules can bind to 1 with simultaneous loss of one or two proton(s), which allows pH-dependent variability in the proportion of substrate-bound structures and following pathways for oxidative activation of the aqua/hydroxo ligands at low thermodynamic and kinetic costs. The resulting bis-oxo intermediates then undergo endothermic O-O radical coupling between two Ru(III)-O(•) units in an anti-coplanar conformation leading to bridged μ-peroxo or μ-superoxo intermediates. The μ-superoxo species can liberate oxygen with the necessity for the preceding binding of a water molecule, which is possible only after four-electron oxidation is completed. The magnitude of catalytic current would be limited by the inherent sluggishness of the hinge-like bending motion of the bridged μ-superoxo complex that opens up the compact, hydrophobic active site of the catalyst and thereby allows water entry under dynamic conditions. On the basis of a newly proposed mechanism, we rationalize the experimentally observed behavior of electrode kinetics with respect to potential and discuss what causes a high overpotential for water oxidation by 1.

  10. Chemistry of ground water in the Silver Springs basin, Florida, with an emphasis on nitrate

    Science.gov (United States)

    Phelps, G.G.

    2004-01-01

    The Silver Springs group, in central Marion County, Florida, has a combined average discharge rate of 796 cubic feet per second and forms the headwaters of the Silver River. The springs support a diverse ecosystem and are an important cultural and economic resource. Concentrations of nitrite-plus-nitrate (nitrate-N) in water from the Main Spring increased from less than 0.5 milligrams per liter (mg/L) in the 1960s to about 1.0 mg/L in 2003. The Upper Floridan aquifer supplies the ground water to support spring discharge. This aquifer is at or near land surface in much of the ground-water basin; nutrients leached at land surface can easily percolate downward into the aquifer. Sources of nitrogen in ground water in the Silver Springs basin include atmospheric deposition, fertilizers used by agricultural and urban activities, and human and animal wastes. During 2000-2001, 56 wells in the area contributing recharge to Silver Springs were sampled for major ions, nutrients, and some trace constituents. Selected wells also were sampled for a suite of organic constituents commonly found in domestic and industrial wastewater and for the ratio of nitrogen isotopes (15N/14N) to better understand the sources of nitrate. Wells were selected to be representative of both confined and unconfined conditions of the Upper Floridan aquifer, as well as a variety of land-use types. Data from this study were compared to data collected from 25 wells in 1989-90. Concentrations of nitrate-N in ground water during this study ranged from less than the detection limit of 0.02 to 12 mg/L, with a median of 1.2 mg/L. For data from 1989-90, the range was from less than 0.02 to 3.6 mg/L, with a median of 1.04 mg/L. Water from wells in agricultural land-use areas had the highest median nitrate-N concentration (1.7 mg/L), although it is uncertain if the 12 mg/L maximum concentration was influenced by land-use activities or proximity to a septic tank. The median value for all urban land-use areas was

  11. The acute toxicity of major ion salts to Ceriodaphnia dubia: I. Influence of background water chemistry

    Science.gov (United States)

    The ions Na+, K+, Ca2+, Mg2+, Cl-, SO42-, and HCO3-/CO32- (referred to as “major ions”) are present in all fresh waters and are physiologically required by aquatic organisms, but can be increased to harmful levels by a variety of anthropogenic activities that speed ge...

  12. Effects of water chemistry on the chronic toxicity of lead to the cladoceran, Ceriodaphnia dubia.

    Science.gov (United States)

    Mager, Edward M; Brix, Kevin V; Gerdes, Robert M; Ryan, Adam C; Grosell, Martin

    2011-03-01

    As the first step toward parameterization of a chronic lead (Pb) biotic ligand model (BLM) for Ceriodaphnia dubia, 7-d toxicity tests were performed in waters modified to evaluate the influences of hardness, DOM (as Suwannee River NOM and Aldrich humic acid (HA)), pH (buffered with 4 mM MOPS) and alkalinity on the chronic toxicity of Pb. Calculated EC(20)s for the control base water test and each of the most extreme modified test waters were as follows in μg L(-1) Pb (95% confidence interval): base water control=45 (14-53), 5 mM CaSO(4)=22 (12-30), 32 mg L(-1) DOM=523 (388-573), 2.5 mM NaHCO(3)=73 (21-120) and pH 6.4 buffered with MOPS=3.9 μg L(-1) Pb (1-5). Results indicate that hardness does not protect against chronic toxicity of Pb to C. dubia, whereas HA does protect at the highest concentration tested (597 μM). Additionally, our findings suggest that low pH increases the chronic toxicity of Pb whereas increased alkalinity is protective. The findings reported herein support the need for a chronic Pb BLM as an alternative approach to hardness-based regulations.

  13. EFFECTS OF WATER CHEMISTRY ON COPPER TOXICITY - WHAT'S MISSING FROM CURRENT MODELS?

    Science.gov (United States)

    Current models for the acute toxicity of cationic metals to aquatic organisms focus on the binding of free metal ions to gill surfaces. This binding, and the resultant toxicity, can be reduced by metal-complexing ligands in the exposure water, which lower the activity of the free...

  14. Relationship between water chemistry and sediment mineralogy in the Cerro Prieto geothermal field: a preliminary report

    Energy Technology Data Exchange (ETDEWEB)

    Valette-Silver, J.N. (Univ. de Perpignan, France); Thompson, J.M.; Ball, J.W.

    1981-01-01

    The chemical compositions of waters collected from the Cerro Prieto geothermal production wells and hydrothermal emanations are different. Compared to the Cerro Prieto well waters, the surficial waters generally contain significantly less potassium, slightly less calcium and chloride, and significantly more magnesium and sulfate. In comparison to the unaltered sediments, the changes in the mineralogy of the altered sediments appear to be controlled by the type of emanation (well, spring, mud pot, geyser, fumarole, or cold pool). However, an increase in quartz and potassium feldspar percentages seems to be characteristic of the majority of the sediments in contact with geothermal fluids. Preliminary attempts to model the chemical processes occurring in the Cerro Prieto geothermal field using chemical equilibrium calculations are reported. For this purpose the chemical compositions of thermal waters (well and surficial emanation) were used as input data to make calculations with SOLMNEQ and WATEQ2 computer programs. Then the theoretical mineral composition of altered sediments was predicted and compared to the mineralogy actually observed in the solid samples.

  15. Support on water chemistry and processes for nuclear power plant auxiliary systems

    Energy Technology Data Exchange (ETDEWEB)

    Chocron, M.; Becquart, E.; La Gamma, A.M.; Schoenbrod, B. [Unidad de Actividad Quimica, Gcia. Centro Atomico Constituyentes, Comision Nacional de Energia, Buenos Aires (Argentina); Allemandi, W.; Fernandez, A.N.; Ovando, L. [Central Nuclear Embalse, Nucleoelectrica Argentina S.A. (Argentina)

    2002-07-01

    In particular PHWRs have a system devoted to the purification and upgrading of the collected heavy water leaks. The purification train is fed with different degradation ratios (D{sub 2}O/H{sub 2}O), activities and impurities. The water is distilled in a packed bed column filled with a mesh type packing. The mesh wire is made of a bronze substrate covered by copper oxides whose current composition has been determined by Moessbauer spectroscopy. With the purpose of minimizing the column stack corrosion, the water is pre-treated in a train consisting of an activated charcoal bed-strong cationic-anionic resin and a final polishing mixed bed resin. Ionic chemicals like acetic acid (whose provenance is suspected to come from the air treatment/D{sub 2}O recovery system where the regeneration is performed at high temperature) are detected by the conductivity and ion chromatography when they concentrate at the column bottom. Traces of oils are retained by the charcoal bed but some compounds extracted by the aqueous phase are suspected to be responsible for the resins fouling or precursors of potentially aggressive agents inside the distillation column. Those species have been detected and identified by gaseous chromatography-mass spectrometry (GC-MS). In the present work, the identification, evaluation of alternatives for the retention and results compared to the original products present in the water upgrading purification train have been summarized. (authors)

  16. Water in IRC+10216: a genuine formation process by shock-induced chemistry in the inner wind

    CERN Document Server

    Cherchneff, Isabelle

    2010-01-01

    Context: The presence of water in the wind of the extreme carbon star IRC+10216 has been confirmed by the Herschel telescope. The regions where the high-J H2O lines have been detected are close to the star at radii r \\geq 15 R\\ast. Aims: We investigate the formation of water and related molecules in the periodically-shocked inner layers of IRC+10216 where dust also forms and accelerates the wind. Methods: We describe the molecular formation by a chemical kinetic network involving carbon-and oxygen-based molecules. We then apply this network to the physical conditions pertaining to the dust-formation zone which experiences the passage of pulsation- driven shocks between 1 and 5 R\\ast. We solve for a system of stiff, coupled, ordinary, and differential equations. Results: Non-equilibrium chemistry prevails in the dust-formation zone. H2O forms quickly above the photosphere from the synthesis of hydroxyl OH induced by the thermal fragmentation of CO in the hot post-shock gas. The derived abundance with respect t...

  17. Adirondack lakes survey: An interpretive analysis of fish communities and water chemistry, 1984--1987

    Energy Technology Data Exchange (ETDEWEB)

    Baker, J.P. (Baker (Joan P.), Raleigh, NC (USA)); Gherini, S.A.; Munson, R.K. (Tetra Tech, Inc., Pasadena, CA (USA)); Christensen, S.W. (Oak Ridge National Lab., TN (USA)); Driscoll, C.T. (Syracuse Univ., NY (USA)); Gallagher, J. (Adirondack Lakes Survey Corp., Ray Brook, NY (USA)); Newton, R.M. (Smith Coll., Northampton, MA (USA)); Reckhow, K.H. (Duke Univ., Durham, NC (USA)); Schofield, C.L. (Co

    1990-01-01

    The Adirondack Lakes Survey Corporation (ALSC) was formed as a cooperative effort of the New York State Department of Environmental Conservation and the Empire State Electric Energy Research Corporation to better characterize the chemical and biological status of Adirondack lakes. Between 1984 and 1987, the ALSC surveyed 1469 lakes within the Adirondack ecological zone. As a follow-up to the survey, the ALSC sponsored a series of interpretive analyses of the ALSC data base. The primary objectives of these analyses were as follows: Evaluate the influence of mineral acids (from acidic deposition) and nonmineral acids (natural organic acids) on lake pH levels; classify Adirondack lakes according to lake and watershed features expected to influence their responsiveness to changes in acidic deposition; evaluate the sensitivity of Adirondack lakes to changes in environmental conditions, such as changes in mineral acids or dissolved organic carbon concentrations; identify lake characteristics important in explaining the observed present-day status of fish communities in Adirondack lakes, in particular the relative importance of lake acidity; evaluate changes that have occurred over time in Adirondack fish communities and probable causes for these trends by using the available historical data on fish communities in the Adirondacks and the ALSC data base; and determine the degree to which the existing fish resource might be at risk from continued acidic deposition, or might recover if acidity levels were reduced. The basic approach examined relationships observed in the ALSC data base among watershed characteristics, lake chemistry, and fish status. Individual reports are processed separately for the data bases.

  18. Effects of catchment and riparian landscape setting on water chemistry and seasonal evolution of water quality in the upper Han River basin, China.

    Directory of Open Access Journals (Sweden)

    Siyue Li

    Full Text Available Six-year (2005-2010 evolution of water chemistry (Cl(-, NO(3(-, SO(4(2-, HCO(3(-, Na(+, K(+, Ca(2+ and Mg(2+ and their interactions with morphological properties (i.e., slope and area, land cover, and hydrological seasonality were examined to identify controlling factors and processes governing patterns of stream water quality in the upper Han River, China. Correlation analysis and stepwise multiple regression models revealed significant correlations between ions (i.e., Cl(-, SO(4(2-, Na(+ and K(+ and land cover (i.e., vegetation and bare land over the entire catchment in both high- and low-flow periods, and in the buffer zone the correlation was much more stronger in the low-flow period. Catchment with steeper slope (>15° was negatively correlated with major ions, largely due to multicollinearity of basin characteristics. Land cover within the buffer zone explained slightly less of major elements than at catchment scale in the rainy season, whereas in the dry season, land cover along the river networks in particular this within 100 m riparian zone much better explained major elements rather than this over the entire catchment. Anthropogenic land uses (i.e., urban and agriculture however could not explain water chemical variables, albeit EC, TDS, anthropogenic markers (Cl(-, NO(3(-, SO(4(2, Na(+, K(+ and Ca(2+ significantly increased during 2005-2010, which was corroborated by principal component analyses (PCA that indicated anthropogenic inputs. Observations demonstrated much higher solute concentrations in the industrial-polluted river. Our results suggested that seasonal evolution of water quality in combined with spatial analysis at multiple scales should be a vital part of identifying the controls on spatio-temporal patterns of water quality.

  19. PREFACE: Water Interfaces in Physics Chemistry and Biology: a multi-disciplinary approach

    Science.gov (United States)

    Bellissent-Funel, Marie-Claire; Dore, John

    2009-07-01

    This 5-day meeting, sponsored by the European Science Foundation (ESF) in partnership with the Fonds zur Förderung der wissenschaftlichen Forschung in Österreich (FWF) was organised by Marie-Claire Bellissent-Funel (Lab. Léon Brillouin (CEA-CNRS), CEA Saclay) and John Dore (School of Physical Sciences, University of Kent). It took place in the Universitatszcentrum (University of Innsbruck), in the ski resort of Obergurgl, Austria, from 8-13 December 2007. The main aim of the meeting was to bring together various groups working on the characteristics of water in a wide range of different conditions, particularly in relation to the difference in behaviour of bulk water and water in close proximity to an interface. Another focus was on the properties of 'solid water' and the free time during the afternoon provided a good opportunity for studying ice interfaces in a different context as the snow conditions were good for ski-ing! An outline of the programme is contained in the PDF file associated with this preface. There was a wide representation encompassing 30 countries and 130 scientists drawn from different science disciplines. Furthermore there was a good range of young scientists, who made an excellent contribution to the poster session. There were, of course, many animated discussions away from the conference room and the feedback forms showed that almost everyone (96%!) felt that they had enjoyed the sessions and had learned something new. There was support for a further conference on this theme in the future. Inevitably, many of the speakers presented information that was in preparation for publication elsewhere and therefore our compilation of some papers in this brief report is not fully representative of the range of topics discussed at the meeting. Further information on specific work reported at the meeting can be obtained by following the author list through the Web of Science or by contacting the authors directly. We report eight short papers from the

  20. Effect of ditching operations on stream-water chemistry in a boreal forested catchment.

    Science.gov (United States)

    Aström, M; Aaltonen, E K; Koivusaari, J

    2001-11-12

    The effects of ditching of boreal forest land on stream-water quality and quantity was assessed by comparing, over a 4-year-period, the physicochemical properties of the water in two small streams (western Finland), one whose catchment was ditched for forestry halfway through the sampling period and another nearby (control) stream whose catchment was not ditched ('paired catchment method'). While the artificial drainage did not have any significant effect on the hydrograph, it resulted in an increase in the aquatic concentrations of Mn, Ca, Mg, suspended material and alkalinity, a decrease in the concentrations of TOC and H3O+, while for Al and Fe there was a change in control mechanisms. The concentration and control changes after ditching are related to changes in hydrological pathways and to the exposure of both organic (peat) and inorganic (mineral soil) layers on the ditch slopes.

  1. Seasonal variations of hydrogen peroxide and water vapor on Mars: Further indications of heterogeneous chemistry

    Science.gov (United States)

    Encrenaz, T.; Greathouse, T. K.; Lefèvre, F.; Montmessin, F.; Forget, F.; Fouchet, T.; DeWitt, C.; Richter, M. J.; Lacy, J. H.; Bézard, B.; Atreya, S. K.

    2015-06-01

    We have completed our seasonal monitoring of hydrogen peroxide and water vapor on Mars using ground-based thermal imaging spectroscopy, by observing the planet in March 2014, when water vapor is maximum, and July 2014, when, according to photochemical models, hydrogen peroxide is expected to be maximum. Data have been obtained with the Texas Echelon Cross Echelle Spectrograph (TEXES) mounted at the 3 m-Infrared Telescope Facility (IRTF) at Maunakea Observatory. Maps of HDO and H2O2 have been obtained using line depth ratios of weak transitions of HDO and H2O2 divided by CO2. The retrieved maps of H2O2 are in good agreement with predictions including a chemical transport model, for both the March data (maximum water vapor) and the July data (maximum hydrogen peroxide). The retrieved maps of HDO are compared with simulations by Montmessin et al. (2005, J. Geophys. Res., 110, 03006) and H2O maps are inferred assuming a mean martian D/H ratio of 5 times the terrestrial value. For regions of maximum values of H2O and H2O2, we derive, for March 1 2014 (Ls = 96°), H2O2 = 20+/-7 ppbv, HDO = 450 +/-75 ppbv (45 +/-8 pr-nm), and for July 3, 2014 (Ls = 156°), H2O2 = 30+/-7 ppbv, HDO = 375+/-70 ppbv (22+/-3 pr-nm). In addition, the new observations are compared with LMD global climate model results and we favor simulations of H2O2 including heterogeneous reactions on water-ice clouds.

  2. Decadal oscillations of the aquatic chemistry of river waters in Latvia

    Science.gov (United States)

    Porshnov, Dmitry; Klavins, Maris

    2016-10-01

    Water quality changes of surface waters can be used to assess human impact intensity, but of importance is to consider also impacts of climate change/variability and naturally occurring changes of environmental quality. In Latvia, during the recent decades a major reduction of anthropogenic pressure has happened due to restructuring of economy and industrial production, resulting in major decrease of loading of many groups of pollutants. However, trends and driving factors for other groups of substances have not been much studied. Long term (1980-2012) results of hydrochemical monitoring, performed in rivers of Latvia, are analysed during this study in connection with long-term sets of hydrological and heliophysical data, using standard statistical approaches. Our results indicate that variation of some hydrochemical values, for example COD and total Fe, show clearly visible decadal oscillated character, while variation of some other values, for example phosphate P and total P, show some individual characteristics of decadal oscillations. These results indicate the presence of a large scale, geochemical and geophysical significant process: multiannual pulse of catchment, driven by variation of solar irradiance through complex interactions between global atmospheric circulation, groundwater and surface waterbodies. The process described in our study is significant from a geochemical point of view and must be taken into account in prediction of water quality and quantity. Impacts of natural processes should be considered in the planning of environmental policy.

  3. A computational chemistry investigation of the mechanism of the water-assisted decomposition of trichloroethylene oxide.

    Science.gov (United States)

    Huang, Jinqing; Yeung, Chi Shun; Ma, Jiani; Gayner, Emma R; Phillips, David Lee

    2014-03-06

    Trichloroethylene oxide is a downstream product in the oxidative metabolism of trichloroethylene (TCE) and it may be involved in cytochrome P450 inactivation, protein function destruction, and nucleic acid base alkalization. To explore the hydrolysis mechanism of the decomposition of TCE oxide, an investigation using Second-order Møller-Plesset perturbation theory in conjunction with density functional theory has been conducted to analyze the effect of the water solvation shell on probable reaction steps. The decomposition of TCE oxide is accelerated by coordinated water molecules (up to seven), which reveals that water molecules can help to solvate the TCE oxide molecule and activate the release of the Cl(-) leaving group. After the opening of the epoxide ring, several pathways are proposed to account for the dehalogenation step along with the formation of CO as well as three carboxylic acids (formic acid, glyoxylic acid, and dichloroacetic acid). The predominant pathways were examined by comparing the computed activation energies for the formation of the products to each other for the possible reaction steps examined in this work. After rationally analyzing the computational results, the ring-opening reaction has been identified as the rate-determining step. The rate constant estimated for the TCE oxide decomposition from the calculations performed here was found to be reasonably consistent with previous experimental observations reported in the literature.

  4. In-plant material test experience under hydrogen water chemistry at a Japanese BWR plant

    Energy Technology Data Exchange (ETDEWEB)

    Ando, Masami; Koshiishi, Masato; Kato, Takahiko [Hitachi Ltd., Ibaraki (Japan). Hitachi Works; Abe, Ayumi; Sekiguchi, Masahiko; Takiguchi, Hideki

    1999-07-01

    Hydrogen injection technology has been applied to Japanese domestic aged BWR plants since 1994 to mitigate corrosive environment regarding Intergranular Stress Corrosion Cracking (IGSCC) of Reactor Internals (RINs). The Tsuruga Unit-1 plant has also been operated with this technology since 1997, considering suppression of radiation increase in the main steam piping system besides mitigation of corrosive environment in the reactor; the hydrogen injection rate in the feed water was about 0.5 ppm. In order to confirm the effects of the hydrogen injection on suppression of SCC susceptibility of the RIN materials, several in-plant material tests have been conducted using the reactor water clean up system (RWCU). Cyclic-Slow Strain Rate Tensile (C-SSRT) test, Slow Strain Rate Tensile (SSRT) test and Compact Tension (CT) test were performed in the test facilities which were installed at the sampling line from the RWCU. Evaluation of SCC life by means of the C-SSRT test was the first application as an accelerated SCC test for in-plant material tests. It was confirmed that the hydrogen injection in the feed water has a good mitigation effects on IGSCC performance of the RIN materials. Results will be discussed from a viewpoint of the test condition such as total oxidant, ECP, conductivity and loading/unloading. (author)

  5. Calculation of Pourbaix Diagrams for C22 in Various Well Water Chemistries

    Energy Technology Data Exchange (ETDEWEB)

    Kaufman, L

    2002-10-02

    Design and Fabrication of the Waste Package for the Yucca Mountain Waste Package represents a formidable challenge of the total knowledge that exists today concerning the properties of a wide variety of materials systems. During the past few years considerable successes have been achieved by employing the techniques of the new ''Computational Thermodynamics'' CT[1 ] to address some of the most critical problems of phase stability with substantial success. In particular, phase stability in Alloy C22 which is a complex 10 component alloy in order to define the temperature dependence of the solidification, welding, heat treatment and transformation kinetics of the condensed liquid, fcc. Sigma, P-Phase and Ni{sub 2}Cr phases are very well described when the modern CT software and databases are applied. The present report provides a description of current progress in the application of this technique to define and detail the corrosion behavior of C-22 by using the Thermo-Calc software and data bases to apply the classic methods devised in the last century by Marcell Pourbaix[2] to C-22 in Simulated J-13 well waters (SAW) simulated acidic waters, SCW, simulated concentrated water and (BSW).The advantages of such a development is that it could provide substantial insight into methods for predicting corrosion behavior in critical components of the Waste Package that will have to function predictably for many tens of thousands of years.

  6. Seasonality of Water Chemistry, Carbonate Production, and Biometric Features of Two Species of Chara in a Shallow Clear Water Lake

    Directory of Open Access Journals (Sweden)

    Andrzej Pukacz

    2014-01-01

    Full Text Available The objective of this study was to analyze the temporal variability of biometric features and the carbonate production of two charophytes: Chara polyacantha A. Braun and Chara rudis A. Braun against the background of the physical-chemical properties of water. The investigation was carried out in a small, mid-forest Lake Jasne (western Poland. It is a polymictic, mesotrophic, hardwater ecosystem dominated by charophyte vegetation. Each month, 10 individuals of each species were characterized in terms of morphometric features, fresh and dry weight, and the percentage of calcium carbonate. Additionally, physical-chemical parameters of the water were studied. The results of physical-chemical analyses indicated similar habitat conditions for both species. Despite smaller dry weight C. polyacantha was characterized by greater morphological variability and higher rates of growth and percentage share of calcium carbonate in dry mass than C. rudis. The percentage of calcium carbonates in dry mass did not differ significantly between the species and exceeded 60%, reaching the maximum (76% in C. polyacantha in July and August. For both species, distinct correlations between the structure of biomass and morphological features were found. The obtained results show the great importance of charophyte vegetation in carbon cycling and functioning of lake ecosystems.

  7. Singlet oxygen chemistry in water. 2. Photoexcited sensitizer quenching by O2 at the water-porous glass interface.

    Science.gov (United States)

    Giaimuccio, Jovan; Zamadar, Matibur; Aebisher, David; Meyer, Gerald J; Greer, Alexander

    2008-12-11

    Insight into the O2 quenching mechanism of a photosensitizer (static or dynamic) would be useful for the design of heterogeneous systems to control the mode of generation of 1O2 in water. Here, we describe the use of a photosensitizer, meso-tetra(N-methyl-4-pyridyl)porphine (1), which was adsorbed onto porous Vycor glass (PVG). A maximum loading of 1.1 x 10(-6) mol 1 per g PVG was achieved. Less than 1% of the PVG surface was covered with photosensitizer 1, and the penetration of 1 reaches a depth of 0.32 mm along all faces of the glass. Time-resolved measurements showed that the lifetime of triplet 1*-ads was 57 microseconds in water. Triplet O2 quenched the transient absorption of triplet 1*-ads; for samples containing 0.9 x 10(-6)-0.9 x 10(-8) mol 1 adsorbed per g PVG, the Stern-Volmer constant, K(D), ranged from 23,700 to 32,100 M(-1). The adduct formation constant, Ks, ranged from 1310 to 510 M(-1). The amplitude of the absorption at 470 nm decreased slightly (by about 0.1) with increased O2 concentrations. Thus, the quenching behavior of triplet 1*-ads by O2 was proposed to be strongly dependent on dynamic quenching. Only approximately 10% of the quenching was attributed to the static quenching mechanism. The quenching of triplet 1*-ads was similar to that observed for photosensitizers in homogeneous solution which are often quenched dynamically by O2.

  8. Controls on the water chemistry of some springs in a volcanic terrain, Nayarit, Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Hemming, N.G.

    1985-01-01

    Dissolution and alteration of minerals and glass in fresh rock, and the extensive occurrence of amorphous residues and precipitates in the weathered rock, control the spring water composition of two volcanoes located in the northwestern segment of the Mexican Volcanic Belt. SEM photomicrographs reveal dissolution and alteration features on phenocrysts that include crystallographically oriented etch pits, and high Al and Fe residues. Vessicles in glass appear to be coalescing to form large voids. Amorphous products are Al-Fe-Si oxides and hydroxides and include allophane and other pseudo-crystalline products. No clay minerals occur in concentrations above the detection limit of an XRD. Silica, sodium and potassium are released into solution at the fresh rock/weathered rock interface. Silica appears to reach a maximum of 100 ppm due to buffering by amorphous silica precipitates. Sinks for potassium may occur deep in the weathering profile on some rock types as Na/K released upon weathering is significantly lower than that found in solution. The anomolously high concentrations of magnesium and calcium in the groundwater and weathered rock, is an indication that they are being released along the flow path and may be adsorbed onto clay-size material where the water emerges through the soil zone.

  9. Low-temperature chemistry between water and hydroxyl radicals: H/D isotopic effects

    CERN Document Server

    Lamberts, T; Puletti, F; Ioppolo, S; Cuppen, H M; Linnartz, H

    2015-01-01

    Sets of systematic laboratory experiments are presented -- combining Ultra High Vacuum cryogenic and plasma-line deposition techniques -- that allow us to compare H/D isotopic effects in the reaction of H2O (D2O) ice with the hydroxyl radical OD (OH). The latter is known to play a key role as intermediate species in the solid-state formation of water on icy grains in space. The main finding of our work is that the reaction H2O + OD --> OH + HDO occurs and that this may affect the HDO/H2O abundances in space. The opposite reaction D2O + OH --> OD + HDO is much less effective, and also given the lower D2O abundances in space not expected to be of astronomical relevance. The experimental results are extended to the other four possible reactions between hydroxyl and water isotopes and are subsequently used as input for Kinetic Monte Carlo simulations. This way we interpret our findings in an astronomical context, qualitatively testing the influence of the reaction rates.

  10. Water nano-hydrodynamics: The interplay between interfacial viscosity, slip and chemistry

    Science.gov (United States)

    Chiu, Hsiang-Chih; Ortiz-Young, Deborah; Riedo, Elisa

    2012-02-01

    The understanding and the ability to manipulate fluids at the nanoscale is a matter of continuously growing scientific and technological interest. Fluid flow in nano-confined geometries is relevant for biology, polymer science and geophysics. The applications range from gene sequencing to protein segregation, cell sorting, sensors, nanotribology and diffusion through porous media. Here, we present experiments which show how the interfacial viscosity of water strongly depends on the wetting properties of the confining surfaces. This dependence is fully explained by considering water slippage at the stationary solid surface. The interfacial viscous forces as a function of six surfaces with different wettability are fitted with a modified form of the Newtonian definition of viscosity, which takes into consideration the fluid slip. This simple relationship can explain the viscosity measurements and permits us to extract a ``slip parameter'' for each investigated surface. This slip parameter is found to increase with the static contact angle of the solid surface as expected from previous work, bringing clear evidence of the relationship between viscosity and slip.

  11. A mini review on the chemistry and catalysis of the water gas shift reaction

    CERN Document Server

    Zhao, Zhun

    2014-01-01

    Water gas shift (WGS) reaction is a chemical reaction in which carbon monoxide reacts with water vapor to form carbon dioxide and hydrogen. It is an important reaction industrially used in conjunction with steam reforming of hydrocarbons for the production of high purity hydrogen. Grenoble et al examined the roles of both active metals and metal oxide support on the kinetics of the WGS reaction. They found out that the turn over numbers of various Al2O3 supported transition metals decreased in the trend of Cu, Re, Co, Ru, Ni, Pt, Os, Au, Fe, Pd, Rh, and Ir, which corresponds nicely to the observed volcano shaped correlation between catalytic activities and respective CO adsorption heat. This is a strong indication that CO gets activated on the metal surface during the reaction and different metals have different activation energies. The authors also observed that the turn over number of Pt/Al2O3 was one order of magnitude higher than that of Pt/SiO2, indicating a strong support effect, which the authors ascri...

  12. Water channel proteins: from their discovery in 1985 in Cluj-Napoca, Romania, to the 2003 Nobel Prize in Chemistry.

    Science.gov (United States)

    Benga, Gh

    2006-10-30

    small indeed, of The New Land was Columbus; later, others, including Amerigo Vespucci (from whom the name derived), have better "seen" and in the subsequent years many explorers discovered the complexity of the Americas. Consequently, the initial discovery of the first water channel by Benga's group must be properly credited; the omission of Gheorghe Benga from the 2003 Nobel Prize in Chemistry (half of which was awarded to Peter Agre "for the discovery of the water channels") was a new mistake in the award of Nobel Prizes. Benga's claim is presented on the web site of the Ad Astra Association (www.ad-astra.ro/benga). As can be seen on this site his recognition as a discoverer of the first water channel protein from the human RBC membrane is growing. Thousands of science-related professionals from hundreds of academic and research units, as well as participants in several international scientific events, have signed as supporters of Benga; his priority is also mentioned in several comments on the 2003 Nobel Prize as presented on the site.

  13. Chemistry and isotopic composition of precipitation and surface waters in Khumbu valley (Nepal Himalaya): N dynamics of high elevation basins.

    Science.gov (United States)

    Balestrini, Raffaella; Polesello, Stefano; Sacchi, Elisa

    2014-07-01

    We monitored the chemical and isotopic compositions of wet depositions, at the Pyramid International Laboratory (5050 ma.s.l.), and surrounding surface waters, in the Khumbu basin, to understand precipitation chemistry and to obtain insights regarding ecosystem responses to atmospheric inputs. The major cations in the precipitation were NH4(+) and Ca(2+), whereas the main anion was HCO3(-), which constituted approximately 69% of the anions, followed by NO3(-), SO4(2-) and Cl(-). Data analysis suggested that Na(+), Cl(-) and K(+) were derived from the long-range transport of marine aerosols. Ca(2+), Mg(2+) and HCO3(-) were related to rock and soil dust contributions and the NO3(-) and SO4(2-) concentrations were derived from anthropogenic sources. Furthermore, NH4(+) was derived from gaseous NH3 scavenging. The isotopic composition of weekly precipitation ranged from -1.9 to -23.2‰ in δ(18)O, and from -0.8 to -174‰ in δ(2)H, with depleted values characterizing the central part of the monsoon period. The chemical composition of the stream water was dominated by calcite and/or gypsum dissolution. However, the isotopic composition of the stream water did not fully reflect the composition of the monsoon precipitation, which suggested that other water sources contributed to the stream flow. Precipitation contents for all ions were the lowest ones among those measured in high elevation sites around the world. During the monsoon periods the depositions were not substantially influenced by anthropogenic inputs, while in pre- and post-monsoon seasons the Himalayas could not represent an effective barrier for airborne pollution. In the late monsoon phase, the increase of ionic contents in precipitation could also be due to a change in the moisture source. The calculated atmospheric N load (0.30 kg ha(-1) y(-1)) was considerably lower than the levels that were measured in other high-altitude environments. Nevertheless, the NO3(-) concentrations in the surface waters

  14. A STUDY ON LEGIONELLA PNEUMOPHILA, WATER CHEMISTRY, AND ATMOSPHERIC CONDITIONS IN COOLING TOWERS AT THE SAVANNAH RIVER SITE

    Energy Technology Data Exchange (ETDEWEB)

    Smith, C.; Brigmon, R.

    2009-10-20

    elevated Legionella concentrations when the dew point temperature was high--a summertime occurrence. However, analysis of the three years of Legionella monitoring data of the 14 different SRS Cooling Towers demonstrated that elevated concentrations are observed at all temperatures and seasons. The objective of this study is to evaluate the ecology of L. pneumophila including serogroups and population densities, chemical, and atmospheric data, on cooling towers at SRS to determine whether relationships exist among water chemistry, and atmospheric conditions. The goal is to more fully understand the conditions which inhibit or encourage L. pneumophila growth and supply this data and associated recommendations to SRS Cooling Tower personnel for improved management of operation. Hopefully this information could then be used to help control L. pneumophila growth more effectively in SRS cooling tower water.

  15. Atmospheric Deposition and Surface-Water Chemistry in Mount Rainier and North Cascades National Parks, U.S.A., Water Years 2000 and 2005-2006

    Science.gov (United States)

    Clow, David W.; Campbell, Donald H.

    2008-01-01

    High-elevation aquatic ecosystems in Mount Rainier and North Cascades National Parks are highly sensitive to atmospheric deposition of nitrogen and sulfur. Thin, rocky soils promote fast hydrologic flushing rates during snowmelt and rain events, limiting the ability of basins to neutralize acidity and assimilate nitrogen deposited from the atmosphere. Potential effects of nitrogen and sulfur deposition include episodic or chronic acidification of terrestrial and aquatic ecosystems. In addition, nitrogen deposition can cause eutrophication of water bodies and changes in species composition in lakes and streams. This report documents results of a study performed by the U.S. Geological Survey, in cooperation with the National Park Service, of the effects of atmospheric deposition of nitrogen and sulfur on surface-water chemistry in Mount Rainier and North Cascades National Parks. Inorganic nitrogen in wet deposition was highest in the vicinity of North Cascades National Park, perhaps due to emissions from human sources and activities in the Puget Sound area. Sulfur in wet deposition was highest near the Pacific coast, reflecting the influence of marine aerosols. Dry deposition generally accounted for less than 30 percent of wet plus dry inorganic nitrogen and sulfur deposition, but occult deposition (primarily fog) represents a potentially substantial unmeasured component of total deposition. Trend analyses indicate inorganic nitrogen in wet deposition was relatively stable during 1986-2005, but sulfur in wet deposition declined substantially during that time, particularly after 2001, when emissions controls were added to a large powerplant in western Washington. Surface-water sulfate concentrations at the study site nearest the powerplant showed a statistically significant decrease between 2000 and 2005-06, but there was no statistically significant change in alkalinity, indicating a delayed response in surface-water alkalinity. Seasonal patterns in surface-water

  16. Participation in the 2001 IAEA interlaboratory comparison on geothermal water chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Joe, Kih Soo; Choi, Kwang Soon; Han, Sun Ho; Suh, Moo Yul; Jeon, Young Shin; Choi, Ke Chun; Pyo, Hyung Yul; Kim, Yong Bok; Kim, Jong Gu; Kim, Won Ho [Korea Atomic Energy Research Institute, Taejeon (Korea)

    2002-04-01

    Korea Atomic Energy Research Institute Analytical laboratory participated in the 2001 IAEA Interlaboratory Comparison on chemical analysis of Geothermal Water containing high salinity organized by IAEA Hydrology Laboratory(INT/0/060). 14 items such as pH, electroconductivity, HCO{sub 3}, Cl, F, SO{sub 4}, SiO{sub 2}, B, Li, Na, K, Ca, Mg were analyzed. The result of this program showed that Korea Atomic Energy Research Institute laboratory was ranked within 15% range from top level. Major analytical methods were applied for this activity such as ICP-AES, AAS, IC, pH meter, conductometer and acid titration. 8 refs., 48 figs., 9 tabs. (Author)

  17. Spatio-temporal variation in stream water chemistry in a tropical urban watershed

    Directory of Open Access Journals (Sweden)

    Alonso Ramírez

    2014-06-01

    Full Text Available Urban activities and related infrastructure alter the natural patterns of stream physical and chemical conditions. According to the Urban Stream Syndrome, streams draining urban landscapes are characterized by high concentrations of nutrients and ions, and might have elevated water temperatures and variable oxygen concentrations. Here, we report temporal and spatial variability in stream physicochemistry in a highly urbanized watershed in Puerto Rico. The main objective of the study was to describe stream physicochemical characteristics and relate them to urban intensity, e.g., percent impervious surface cover, and watershed infrastructure, e.g., road and pipe densities. The Río Piedras Watershed in the San Juan Metropolitan Area, Puerto Rico, is one of the most urbanized regions on the island. The Río Piedras presented high solute concentrations that were related to watershed factors, such as percent impervious cover. Temporal variability in ion concentrations lacked seasonality, as did all other parameters measured except water temperature, which was lower during winter and highest during summer, as expected based on latitude. Spatially, stream physicochemistry was strongly related to watershed percent impervious cover and also to the density of urban infrastructure, e.g., roads, pipe, and building densities. Although the watershed is serviced by a sewage collection system, illegal discharges and leaky infrastructure are probably responsible for the elevated ion concentration found. Overall, the Río Piedras is an example of the response of a tropical urban watershed after major sewage inputs are removed, thus highlighting the importance of proper infrastructure maintenance and management of runoff to control ion concentrations in tropical streams.

  18. Spent fuel dissolution rates as a function of burnup and water chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Gray, W.J.

    1998-06-01

    To help provide a source term for performance-assessment calculations, dissolution studies on light-water-reactor (LWR) spent fuel have been conducted over the past few years at Pacific Northwest National Laboratory in support of the Yucca Mountain Site Characterization Project. This report describes that work for fiscal years 1996 through mid-1998 and includes summaries of some results from previous years for completeness. The following conclusions were based on the results of various flowthrough dissolution rate tests and on tests designed to measure the inventories of {sup 129}I located within the fuel/cladding gap region of different spent fuels: (1) Spent fuels with burnups in the range 30 to 50 MWd/kgM all dissolved at about the same rate over the conditions tested. To help determine whether the lack of burnup dependence extends to higher and lower values, tests are in progress or planned for spent fuels with burnups of 13 and {approximately} 65 MWd/kgM. (2) Oxidation of spent fuel up to the U{sub 4}O{sub 9+x} stage does not have a large effect on intrinsic dissolution rates. However, this degree of oxidation could increase the dissolution rates of relatively intact fuel by opening the grain boundaries, thereby increasing the effective surface area that is available for contact by water. From a disposal viewpoint, this is a potentially more important consideration than the effect on intrinsic rates. (3) The gap inventories of {sup 129}I were found to be smaller than the fission gas release (FGR) for the same fuel rod with the exception of the rod with the highest FGR. Several additional fuels would have to be tested to determine whether a generalized relationship exists between FGR and {sup 129}I gap inventory for US LWR fuels.

  19. Making Water Chemistry Data From Volcano-Hydrothermal Systems Accessible Using Open Source Tools

    Science.gov (United States)

    Venezky, D. Y.; Mariner, R. H.; Hurwitz, S.; Evans, W. C.

    2004-12-01

    Chemical and isotopic data collected over several decades by the U.S. Geological Survey from volcano-hydrothermal systems were recently organized into a web-accessible database for public use. The data were collected by members of the Barnes and/or Mariner projects and were supplemented with data from samples submitted for analysis by other researchers with similar interests. The data are primarily chemical and isotopic analyses of waters (thermal, mineral, or fresh) and associated gas (free and/or dissolved) collected from hot springs, mineral springs, cold springs, geothermal wells, fumaroles, and gas seeps. Additional data for a few streams, lakes, and oil wells are included. The web site follows a multi-stage design, first allowing for basic access to the MySQL database, then a user-friendly GIS (Geographic Information System) interface, and finally access to additional documentation and searching features. The initial web pages allow the user to choose the type of data (site, physical parameters, major and minor dissolved constituents, dissolved and free gas composition, water isotopes, and other isotopes) and the sample location. The data are then shown in a table that can be downloaded in several formats. The second stage of the project added an open-source GIS package called WorldKit, which gives easy-to-code and easy-to-use clickable icons on a base map using XML (Extensible Markup Language). WorldKit is also adding a zoom interface (zoomify) that uses new technology to reduce the display time. The final stage of the project involves more complex queries, alternative data presentation, and integrated background information. The more complex queries allow users to select multiple types of data from multiple sites. The data can be found at http://hotspringchem.wr.usgs.gov/.

  20. Effect of water chemistry on environmentally assisted cracking of alloy 600 in simulated primary side PWR environments

    Energy Technology Data Exchange (ETDEWEB)

    Koenig, M. [Studsvik Nuvlear (Sweden); Lidar, P. [GSE Power Systems (Sweden); Engstroem, J. [Ringhals NPP (Sweden); Gott, K. [SKI Sweden (Sweden)

    2002-07-01

    Environmental aspects of crack growth due to intergranular stress corrosion cracking (IGSCC) of Alloy 600 in simulated primary side PWR environments have been studied. The purpose of the study was to quantify the effects of the water chemistry (Li, B and H{sub 2} concentrations, and the pH-value by adding KOH) on the crack growth rate, da/dt. 12.5 mm thick compact tension (CT) specimens were used for testing at a constant maximum stress intensity factor in the range of 26-32 MPa{open_square}m. The crack growth was continuously monitored using a direct current potential drop system. Intergranular crack growth due to IGSCC was dominant in the specimens, although there were also small fractions of transgranular cracking. Multivariate analysis was used on the results from the present work together with results from previous tests on the same material. Temperature and the stress intensity were also included as factors in the analysis. A partial least squares regression was developed and interaction effects between the factors were found to affect the crack growth rate. The Partial Least Square regression predicts the observed crack growth rates reasonably well. (authors)

  1. Toxicity of TiO2 nanoparticles to Escherichia coli: effects of particle size, crystal phase and water chemistry.

    Science.gov (United States)

    Lin, Xiuchun; Li, Jingyi; Ma, Si; Liu, Gesheng; Yang, Kun; Tong, Meiping; Lin, Daohui

    2014-01-01

    Controversial and inconsistent results on the eco-toxicity of TiO2 nanoparticles (NPs) are commonly found in recorded studies and more experimental works are therefore warranted to elucidate the nanotoxicity and its underlying precise mechanisms. Toxicities of five types of TiO2 NPs with different particle sizes (10∼50 nm) and crystal phases were investigated using Escherichia coli as a test organism. The effect of water chemistry on the nanotoxicity was also examined. The antibacterial effects of TiO2 NPs as revealed by dose-effect experiments decreased with increasing particle size and rutile content of the TiO2 NPs. More bacteria could survive at higher solution pH (5.0-10.0) and ionic strength (50-200 mg L(-1) NaCl) as affected by the anatase TiO2 NPs. The TiO2 NPs with anatase crystal structure and smaller particle size produced higher content of intracellular reactive oxygen species and malondialdehyde, in line with their greater antibacterial effect. Transmission electron microscopic observations showed the concentration buildup of the anatase TiO2 NPs especially those with smaller particle sizes on the cell surfaces, leading to membrane damage and internalization. These research results will shed new light on the understanding of ecological effects of TiO2 NPs.

  2. Toxicity of TiO2 nanoparticles to Escherichia coli: effects of particle size, crystal phase and water chemistry.

    Directory of Open Access Journals (Sweden)

    Xiuchun Lin

    Full Text Available Controversial and inconsistent results on the eco-toxicity of TiO2 nanoparticles (NPs are commonly found in recorded studies and more experimental works are therefore warranted to elucidate the nanotoxicity and its underlying precise mechanisms. Toxicities of five types of TiO2 NPs with different particle sizes (10∼50 nm and crystal phases were investigated using Escherichia coli as a test organism. The effect of water chemistry on the nanotoxicity was also examined. The antibacterial effects of TiO2 NPs as revealed by dose-effect experiments decreased with increasing particle size and rutile content of the TiO2 NPs. More bacteria could survive at higher solution pH (5.0-10.0 and ionic strength (50-200 mg L(-1 NaCl as affected by the anatase TiO2 NPs. The TiO2 NPs with anatase crystal structure and smaller particle size produced higher content of intracellular reactive oxygen species and malondialdehyde, in line with their greater antibacterial effect. Transmission electron microscopic observations showed the concentration buildup of the anatase TiO2 NPs especially those with smaller particle sizes on the cell surfaces, leading to membrane damage and internalization. These research results will shed new light on the understanding of ecological effects of TiO2 NPs.

  3. Multi-linear regression analysis, preliminary biotic ligand modeling, and cross species comparison of the effects of water chemistry on chronic lead toxicity in invertebrates.

    Science.gov (United States)

    Esbaugh, A J; Brix, K V; Mager, E M; De Schamphelaere, K; Grosell, M

    2012-03-01

    The current study examined the chronic toxicity of lead (Pb) to three invertebrate species: the cladoceran Ceriodaphnia dubia, the snail Lymnaea stagnalis and the rotifer Philodina rapida. The test media consisted of natural waters from across North America, varying in pertinent water chemistry parameters including dissolved organic carbon (DOC), calcium, pH and total CO(2). Chronic toxicity was assessed using reproductive endpoints for C. dubia and P. rapida while growth was assessed for L. stagnalis, with chronic toxicity varying markedly according to water chemistry. A multi-linear regression (MLR) approach was used to identify the relative importance of individual water chemistry components in predicting chronic Pb toxicity for each species. DOC was an integral component of MLR models for C. dubia and L. stagnalis, but surprisingly had no predictive impact on chronic Pb toxicity for P. rapida. Furthermore, sodium and total CO(2) were also identified as important factors affecting C. dubia toxicity; no other factors were predictive for L. stagnalis. The Pb toxicity of P. rapida was predicted by calcium and pH. The predictive power of the C. dubia and L. stagnalis MLR models was generally similar to that of the current C. dubia BLM, with R(2) values of 0.55 and 0.82 for the respective MLR models, compared to 0.45 and 0.79 for the respective BLMs. In contrast the BLM poorly predicted P. rapida toxicity (R(2)=0.19), as compared to the MLR (R(2)=0.92). The cross species variability in the effects of water chemistry, especially with respect to rotifers, suggests that cross species modeling of invertebrate chronic Pb toxicity using a C. dubia model may not always be appropriate.

  4. Insights from gas and water chemistry on the geothermal system of the Domuyo volcanic complex (Patagonia, Argentina)

    Science.gov (United States)

    Tassi, F.; Liccioli, C.; Chiodini, G.; Agusto, M.; Caselli, A. T.; Caliro, S.; Vaselli, O.; Pecoraino, G.

    2015-12-01

    This study focuses on the geochemistry of geothermal fluids discharging from the western flank of the Domuyo volcanic complex (Argentina), which is hosted within an extensional basins that interrupts the Andes at latitudes comprises between 35° and 39°S. The analytical results of gas and water samples collected during three sampling campaigns (2013, 2014 and 2015) are presented and discussed in order to: i) evaluate the equilibrium temperature(s) of the main fluid reservoir, ii) provide information on the origin of the fluid discharges and the secondary processes controlling their chemistry. Geothermometry based on the chemical composition of thermal waters indicates a maximum equilibrium temperature of 220 °C. This temperature, coupled with the measured amount of discharged Cl, suggest that the total energy released from this system is 1.1±0.2 GW. Atmospheric gases from a thick shallow aquifer contaminate most gas emissions, masking the chemical features of the deep fluid component, with the only exception of a jet fumarole located at 3,000 m a.s.l. (Bramadora). The H2O-CO2-CH4-H2-CO-C3H6-C3H8 composition of this gas emission was used to construct a geochemical conceptual model showing that the hydrothermal reservoir is liquid-dominated and thermally stratified, with temperatures ranging from 180 to 270 °C. The helium isotopic ratios (up to 6.8 Ra) and the δ13C-CO2 values (from -7.05 to -7.75 ‰ V-PDB) indicate that mantle degassing represents the dominant primary source for this dormant volcano. These results highlight the huge potential of this system as energy resource for the region. Accordingly, the regional authorities have recently planned and approved an investigation project aimed to provide further insights into the fluid geochemistry and the geostructural assessment in this promising area.

  5. Removal of triazine-based pollutants from water by carbon nanotubes: Impact of dissolved organic matter (DOM) and solution chemistry.

    Science.gov (United States)

    Engel, Maya; Chefetz, Benny

    2016-12-01

    Adsorption of organic pollutants by carbon nanotubes (CNTs) in the environment or removal of pollutants during water purification require deep understanding of the impacts of the presence of dissolved organic matter (DOM). DOM is an integral part of environmental systems and plays a key role affecting the behavior of organic pollutants. In this study, the effects of solution chemistry (pH and ionic strength) and the presence of DOM on the removal of atrazine and lamotrigine by single-walled CNTs (SWCNTs) was investigated. The solubility of atrazine slightly decreased (∼5%) in the presence of DOM, whereas that of lamotrigine was significantly enhanced (by up to ∼70%). Simultaneous introduction of DOM and pollutant resulted in suppression of removal of both atrazine and lamotrigine, which was attributed to DOM-pollutant competition or blockage of adsorption sites by DOM. However the decrease in removal of lamotrigine was also a result of its complexation with DOM. Pre-introduction of DOM significantly reduced pollutant adsorption by the SWCNTs, whereas introduction of DOM after the pollutant resulted in the release of adsorbed atrazine and lamotrigine from the SWCNTs. These data imply that DOM exhibits higher affinity for the adsorption sites than the triazine-based pollutants. In the absence of DOM atrazine was a more effective competitor than lamotrigine for adsorption sites in SWCNTs. However, competition between pollutants in the presence of DOM revealed lamotrigine as the better competitor. Our findings help unravel the complex DOM-organic pollutant-CNT system and will aid in CNT-implementation in water-purification technologies.

  6. ICON-ART-ISO: Implementing water isotopologues into the new chemistry-transport model ICON-ART

    Science.gov (United States)

    Eckstein, Johannes; Ruhnke, Roland; Pfahl, Stephan; Rieger, Daniel; Reinert, Daniel

    2016-04-01

    The stable isotopologues of water can help to understand processes that an airmass has undergone and that have influenced the distribution of water in its different states in the airmass. Measurements alone, by their limited temporal or spatial resolution, are often an insufficient tool for unraveling these processes. An atmospheric model capable of simulating the distribution of HDO and H218O at a high spatio-temporal resolution can therefore be very useful for the interpretation of data and the study of processes. Here, we present ICON-ART-ISO, the implementation of HDO and H218O into the new chemistry-transport model ICON-ART. The core of the model is the new ICOsahedral Non-hydrostatic (ICON) modelling framework (Zaengl et al, 2014, Q. J. R. Meteorol. Soc.), a global model which allows to locally increase resolution. It is used for numerical weather prediction at the German Weather Service (DWD), but is also suitable for climate modelling. The model system ICON-ART (Aerosols and Reactive Trace gases, Rieger et al, 2015 (GMD)) is a two-way coupled extension to ICON, which allows to study the influence of aerosols and trace gases on the state of the atmosphere. We set up ICON-ART-ISO within this framework, following the implementation of COSMOiso (Pfahl et al., 2012 (ACP)), the isotope-enabled version of the COSMO model, the predecessor of ICON. In order to include the isotopologues in the model, the water cycle is doubled diagnostically to mirror all processes dealing with water onto HDO and H218O. Processes where isotopic fractionation has to be considered are the evaporation, the grid-scale formation of clouds and precipitation and processes related to convection. Evaporation is limited to the ocean surfaces in a first step. To consider grid-scale precipitation, the isotopologues have been implemented into the two-moment microphysical scheme by Seifert and Beheng, 2005 (Meteorol. Atmos. Phys.), an extensive scheme considering many processes and four ice

  7. Aspects of the physics and chemistry of water radiolysis by fast neutrons and fast electrons in nuclear reactors

    Energy Technology Data Exchange (ETDEWEB)

    McCracken, D.R. [Atomic Energy of Canada Limited, Chalk River, Ontario (Canada); Tsang, K.T. [Atomic Energy of Canada Limited, Mississauga, Ontario (Canada); Laughton, P.J

    1998-09-01

    Detailed radiation physics calculations of energy deposition have been done for the coolant of CANDU reactors and Pressurized Water Reactors (PWRs). The geometry of the CANDU fuel channel was modelled in detail. Fluxes and energy-deposition rates for neutrons, recoil ions, photons, and fast electrons have been calculated using MCNP4B, WIMS-AECL, and specifically derived energy-transfer factors. These factors generate the energy/flux spectra of recoil ions from fast-neutron energy/flux spectra. The energy spectrum was divided into 89 discrete ranges (energy bins).The production of oxidizing species and net coolant radiolysis can be suppressed by the addition of hydrogen to the coolant of nuclear reactors. It is argued that the net dissociation of coolant by gamma rays is suppressed by lower levels of excess hydrogen than when dissociation is by ion recoils. This has consequences for the modelling of coolant radiolysis by homogeneous kinetics. More added hydrogen is required to stop water radiolysis by recoil ions acting alone than if recoil ions and gamma rays acted concurrently in space and time. Homogeneous kinetic models and experimental data suggest that track overlap is very inefficient in providing radicals from gamma-ray tracks to recombine molecular products in ion-recoil tracks. An inhomogeneous chemical model is needed that incorporates ionizing-particle track structure and track overlap. Such a model does not yet exist, but a number of limiting cases using homogeneous kinetics are discussed. There are sufficient uncertainties and contradictions in the data relevant to the radiolysis of reactor coolant that the relatively high CHC's (critical hydrogen concentration) observed in NRU reactor experiments (compared to model predictions) may be explainable by errors in fundamental data and understanding of water radiolysis under reactor conditions. The radiation chemistry program at CRL has been focused to generate quantitative water-radiolysis data in a

  8. Indicators: Soil Chemistry

    Science.gov (United States)

    The chemical makeup of the soil can provide information on wetland condition, wetland water quality and services being provided by the wetland ecosystem. Analyzing soil chemistry reveals if the soil is contaminated with a toxic chemical or heavy metal.

  9. Influences of water chemistry on the acute toxicity of lead to Pimephales promelas and Ceriodaphnia dubia.

    Science.gov (United States)

    Mager, Edward M; Esbaugh, Andrew J; Brix, Kevin V; Ryan, Adam C; Grosell, Martin

    2011-01-01

    The acute toxicity of lead (Pb) was examined for fathead minnows (Pimephales promelas; 96-h) and daphnids (Ceriodaphnia dubia; 48-h) in waters modified for hardness (as CaSO₄), dissolved organic carbon (DOC; as Aldrich humic acid) and alkalinity (as NaHCO₃) for parameterization of an acute freshwater biotic ligand model (BLM). Additionally, acute (96-h) and chronic (30-d) bioassays were performed for P. promelas to more clearly define the influence of pH (5.5-8.3) on Pb toxicity as modified by addition of HCl or NaOH using an automated titration system. Results indicate that Ca(2+) is protective against acute Pb toxicity to P. promelas but not C. dubia. Strong protection was afforded by DOC and NaHCO(3) against acute Pb toxicity to P. promelas, whereas milder protection was observed for C. dubia with both parameters. Dissolved Pb LC50s from the P. promelas pH bioassays revealed a complex effect of pH on Pb toxicity, likely explained in part by Pb speciation and the competitive interaction of H(+) with ionic Pb(2+). Chronic pH bioassays also demonstrated that 30-d growth is not impaired in fathead minnows at relevant Pb concentrations. The findings reported herein suggest that development of separate BLMs for P. promelas and C. dubia should be considered.

  10. Integrated Ecological River Health Assessments, Based on Water Chemistry, Physical Habitat Quality and Biological Integrity

    Directory of Open Access Journals (Sweden)

    Ji Yoon Kim

    2015-11-01

    Full Text Available This study evaluated integrative river ecosystem health using stressor-based models of physical habitat health, chemical water health, and biological health of fish and identified multiple-stressor indicators influencing the ecosystem health. Integrated health responses (IHRs, based on star-plot approach, were calculated from qualitative habitat evaluation index (QHEI, nutrient pollution index (NPI, and index of biological integrity (IBI in four different longitudinal regions (Groups I–IV. For the calculations of IHRs values, multi-metric QHEI, NPI, and IBI models were developed and their criteria for the diagnosis of the health were determined. The longitudinal patterns of the river were analyzed by a self-organizing map (SOM model and the key major stressors in the river were identified by principal component analysis (PCA. Our model scores of integrated health responses (IHRs suggested that mid-stream and downstream regions were impaired, and the key stressors were closely associated with nutrient enrichment (N and P and organic matter pollutions from domestic wastewater disposal plants and urban sewage. This modeling approach of IHRs may be used as an effective tool for evaluations of integrative ecological river health..

  11. Water chemistry and electrical conductivity database for rivers in Yellowstone National Park, Wyoming

    Science.gov (United States)

    Clor, Laura E.; McCleskey, R. Blaine; Huebner, Mark A.; Lowenstern, Jacob B.; Heasler, Henry P.; Mahony, Dan L.; Maloney, Tim; Evans, William C.

    2012-01-01

    Chloride flux has been used to estimate heat flow in volcanic environments since the method was developed in New Zealand by Ellis and Wilson (1955). The method can be applied effectively at Yellowstone, because nearly all of the water discharged from its thermal features enters one of four major rivers (the Madison, Yellowstone, Snake, and Falls Rivers) that drain the park, and thus integration of chloride fluxes from all these rivers provides a means to monitor the total heat flow from the entire Yellowstone volcanic system (Fournier and others, 1976; Fournier, 1979). Fournier (1989) summarized the results and longterm heat-flow trends from Yellowstone, and later efforts that applied the chloride inventory method to estimate heat flow were described by Ingebritsen and others (2001) and Friedman and Norton (2007). Most recently, the U.S. Geological Survey (USGS), in conjunction with the National Park Service, has provided publicly accessible reports on solute flux, based on periodic sampling at selected locations (Hurwitz and others, 2007a,b). While these studies have provided a wealth of valuable data, winter travel restrictions and the great distances between sites present significant logistical challenges and have limited collection to a maximum of 28 samples per site annually.

  12. Electron-induced chemistry of methyl chloride caged within amorphous solid water

    Science.gov (United States)

    Horowitz, Yonatan; Asscher, Micha

    2013-10-01

    The interaction of low energy electrons (1.0-25 eV) with methyl-chloride (CD3Cl) molecules, caged within Amorphous Solid Water (ASW) films, 10-120 monolayer (ML) thick, has been studied on top of a Ru(0001) substrate under Ultra High Vacuum (UHV) conditions. While exposing the ASW film to 3 eV electrons a static electric field up to 8 × 108 V/m is developed inside the ASW film due to the accumulation of trapped electrons that produce a plate capacitor voltage of exactly 3 V. At the same time while the electrons continuously strike the ASW surface, they are transmitted through the ASW film at currents of ca. 3 × 10-7 A. These electrons transiently attach to the caged CD3Cl molecules leading to C-Cl bond scission via Dissociative Electron Attachment (DEA) process. The electron induced dissociation cross sections and product formation rate constants at 3.0 eV incident electrons at ASW film thicknesses of 10 ML and 40 ML were derived from model simulations supported by Thermal Programmed Desorption (TPD) experimental data. For 3.0 eV electrons the CD3Cl dissociation cross section is 3.5 × 10-16 cm2, regardless of ASW film thickness. TPD measurements reveal that the primary product is deuterated methane (D3CH) and the minor one is deuterated ethane (C2D6).

  13. The Tianjin geothermal field (north-eastern China): Water chemistry and possible reservoir permeability reduction phenomena

    Energy Technology Data Exchange (ETDEWEB)

    Minissale, Angelo; Montegrossi, Giordano; Orlando, Andrea [Institute of Geosciences and Earth Resources, National Research Council of Italy (CNR), Via G. La Pira 4, 50121 Florence (Italy); Borrini, Daniele; Tassi, Franco [Department of Earth Sciences, University of Florence, Via G. La Pira 4, 50121 Florence (Italy); Vaselli, Orlando [Institute of Geosciences and Earth Resources, National Research Council of Italy (CNR), Via G. La Pira 4, 50121 Florence (Italy); Department of Earth Sciences, University of Florence, Via G. La Pira 4, 50121 Florence (Italy); Huertas, Antonio Delgado [Estacion Experimental de Zaidin (CSIC), Prof. Albareda 1, 18008 Granada (Spain); Yang, Jincheng; Cheng, Wanquing [Aode Renewable Energy Research Institute, 90 Weijin South Road, Nankai District, 300381 Tianjin (China); Tedesco, Dario [Department of Environmental Sciences, Second University of Naples, Via Vivaldi 43, Caserta 81100 (Italy); Institute of Environmental Geology and Geo Engineering (CNR), Piazzale A. Moro 5, Roma 00100 (Italy); Poreda, Robert [Department of Earth and Environmental Sciences, University of Rochester, 227 Hutchison Hall, Rochester, NY 14627 (United States)

    2008-08-15

    Injection of spent (cooled) thermal fluids began in the Tianjin geothermal district, north-eastern China, at the end of the 1990s. Well injectivities declined after 3-4 years because of self-sealing processes that reduced reservoir permeability. The study focuses on the factors that may have caused the observed decrease in permeability, using chemical and isotopic data on fluids (water and gas) and mineral phases collected from production and injection wells. The results of data processing and interpretation indicate that (1) it is very unlikely that calcite and silica precipitation is taking place in the reservoir; (2) the Fe- and Zn-rich mineral phases (e.g. sulfides, hydroxides and silicates) show positive saturation indexes; (3) SEM and XRD analyses of filtered material reveal that the latter mineral phases are common; (4) visual observation of casings and surface installations, and of corrosion products, suggests that a poor quality steel was used in their manufacture; (5) significant quantities of solids (e.g. quartz and feldspar crystals) are carried by the geothermal fluid; (6) seasonal changes in fluid composition lead to a reduction in casing corrosion during the summer. It was concluded that the decrease in injectivity in the Tianjin wells is caused only in part by the oxidation of casings, downhole pumps, and surface installations, triggered by free oxygen in the injected fluids; the utilization of better quality steels should drastically reduce this type of corrosion. Self-sealing of pores and fractures by reservoir formation solids and by the Fe-corrosion products suspended in the injected fluids seems to be a more important phenomenon, whose effect could be greatly reduced by installing filtering devices at all sites. (author)

  14. Wood-ash addition on a drained forest peatland in Southern Sweden - Effects on water chemistry; Tillfoersel av biobra ensleaska i tallskog paa en dikad torvmark i soedra Sverige - Effekter paa vattenkemin

    Energy Technology Data Exchange (ETDEWEB)

    Ring, Eva; Broemssen, Claudia von; Losjoe, Katarina; Sikstroem Ulf

    2012-02-15

    Wood ash can be used for forest fertilization on peatlands or for nutrient compensation following intensive harvesting. This project was performed in order to investigate effects on water chemistry of applying wood ash to a Scots pine stand on a drained peatland. Ditch-water chemistry was monitored before and after the application of wood ash. Furthermore, groundwater was collected and chemically analyzed both from the ash-treated peatland and from an adjacent untreated reference peatland. Both short term (a few months) and more long term effects (up to three years after application) were detected on water chemistry

  15. The effect of variable discharge on the inorganic chemistry downstream of a waste water treatment plant, Boulder Creek, Colorado

    Science.gov (United States)

    Antweiler, R. C.; Writer, J. H.; Murphy, S. F.

    2012-12-01

    Researchers investigating the effect of wastewater treatment plant (WWTP) effluent on streams often assume that the magnitude of this effect is constant over time. However, discharge of WWTP effluent frequently follows a distinctive diel pattern. WWTP effluent discharge into Boulder Creek, Colorado, for example, varies by almost 200% over the course of a day. Due to this variation, downstream concentrations of chloride, boron and gadolinium (commonly used "conservative tracers") exhibit major changes over a 24-hour period. In order to determine how effluent discharge variability affects stream chemistry, we performed an evaluation of discharge and inorganic chemistry of the City of Boulder's WWTP and Boulder Creek upstream and downstream of the WWTP (representing a 5.4-km reach). Sodium bromide and Rhodamine WT were used to confirm that the same parcel of water was sampled as it moved downstream. The behavior of inorganic constituents fell into three distinct categories, showing conservative behavior, in-stream loss, or in-stream gain. Accounting for variable effluent discharge, the following inorganic constituents behaved conservatively: Cl, SO4, HCO3, F, B, Ba, Ca, Gd, K, Mg, Rb, Co, Cu, Mo, NO3, P and PO4, Sb, SiO2, Sr and Zn. Inorganic compounds which showed evidence of in-stream loss were Bi, Cr, Cs, Ga, Ge, Hg, Se, and Sn. For these elements, the typical pattern was an almost immediate loss: by the time the water had traveled to the first downstream sampling site, 2.3-km below the WWTP, in-stream reactions appeared to have ceased, and a constant flux was observed at all subsequent sites. We speculate that the near-immediate rates represent precipitation and/or adsorption caused by the change in pH and temperature of the mixing zone. Inorganic constituents that showed evidence of in-stream gain were: Al, As, Cd, Fe, I, Li, Mn, Nb, Pb, Re, Th, U, V, W, and all the rare-earth elements (except Gd). As with the in-stream loss group, most of the reactions occurred

  16. Contrasting roles of water chemistry, lake morphology, land-use, climate and spatial processes in driving phytoplankton richness in the Danish landscape

    DEFF Research Database (Denmark)

    Özkan, Korhan; Jeppesen, Erik; Søndergaard, Martin;

    2013-01-01

    were performed on permuted data 1,000 times. The local environment was described by lake water chemistry, lake morphology, land-use in lake catchments, and climate. Analysis of the effects of four groups of environmental factors on the richness of the main groups of phytoplankton revealed contrasting...... patterns. Lake water chemistry was the strongest predictor of phytoplankton richness for all groups, while lake morphology also had a strong influence on Bacillariophyceae, Cyanobacteria, Dinophyceae, and Euglenophyceae richness. Climate and land-use in catchments contributed only little to the explained...... variation in phytoplankton richness, although both factors had a significant effect on Bacillariophyceae richness. Notably, total nitrogen played a more important role for phytoplankton richness than total phosphorus. Overall, models accounted for ca. 30% of the variation in genus richness for all...

  17. Conference on the Physics, Chemistry and Biology of Water (3rd) Held in West Dover, Vermont on October 16-19, 2008 (Abstracts)

    Science.gov (United States)

    2008-10-27

    confinement, photocatalytic water splitting, recyclable hydrogen, thermoluminescence, nanofluids, nanochannels. aqueous hydroxide ion transport , IR...11:50 Andrei Tokmakoff MIT The dynamics of aqueous hydroxide ion transport from 2D IR spectroscopy 12:25 Lunch TOGETHER Session F-II Short-range...aqueous solutions of Homeopathic Medicine V.Elia and E.Napoli Department of Chemistry University "Federico IT’ of Naples , Complesso Universitario di

  18. A synthesis of atmospheric mercury depletion event chemistry linking atmosphere, snow and water

    Directory of Open Access Journals (Sweden)

    A. Steffen

    2007-07-01

    Full Text Available It was discovered in 1995 that, during the spring time, unexpectedly low concentrations of gaseous elemental mercury (GEM occurred in the Arctic air. This was surprising for a pollutant known to have a long residence time in the atmosphere; however conditions appeared to exist in the Arctic that promoted this depletion of mercury (Hg. This phenomenon is termed atmospheric mercury depletion events (AMDEs and its discovery has revolutionized our understanding of the cycling of Hg in Polar Regions while stimulating a significant amount of research to understand its impact to this fragile ecosystem. Shortly after the discovery was made in Canada, AMDEs were confirmed to occur throughout the Arctic, sub-Artic and Antarctic coasts. It is now known that, through a series of photochemically initiated reactions involving halogens, GEM is converted to a more reactive species and is subsequently associated to particles in the air and/or deposited to the polar environment. AMDEs are a means by which Hg is transferred from the atmosphere to the environment that was previously unknown. In this article we review the history of Hg in Polar Regions, the methods used to collect Hg in different environmental media, research results of the current understanding of AMDEs from field, laboratory and modeling work, how Hg cycles around the environment after AMDEs, gaps in our current knowledge and the future impacts that AMDEs may have on polar environments. The research presented has shown that while considerable improvements in methodology to measure Hg have been made the main limitation remains knowing the speciation of Hg in the various media. The processes that drive AMDEs and how they occur are discussed. As well, the roles that the snow pack, oceans, fresh water and the sea ice play in the cycling of Hg are presented. It has been found that deposition of Hg from AMDEs occurs at marine coasts and not far inland and that a fraction of the deposited Hg does not

  19. Physical and biological controls on the carbonate chemistry of coral reef waters: effects of metabolism, wave forcing, sea level, and geomorphology.

    Directory of Open Access Journals (Sweden)

    James L Falter

    Full Text Available We present a three-dimensional hydrodynamic-biogeochemical model of a wave-driven coral-reef lagoon system using the circulation model ROMS (Regional Ocean Modeling System coupled with the wave transformation model SWAN (Simulating WAves Nearshore. Simulations were used to explore the sensitivity of water column carbonate chemistry across the reef system to variations in benthic reef metabolism, wave forcing, sea level, and system geomorphology. Our results show that changes in reef-water carbonate chemistry depend primarily on the ratio of benthic metabolism to the square root of the onshore wave energy flux as well as on the length and depth of the reef flat; however, they are only weakly dependent on channel geometry and the total frictional resistance of the reef system. Diurnal variations in pCO(2, pH, and aragonite saturation state (Ω(ar are primarily dependent on changes in net production and are relatively insensitive to changes in net calcification; however, net changes in pCO(2, pH, and Ω(ar are more strongly influenced by net calcification when averaged over 24 hours. We also demonstrate that a relatively simple one-dimensional analytical model can provide a good description of the functional dependence of reef-water carbonate chemistry on benthic metabolism, wave forcing, sea level, reef flat morphology, and total system frictional resistance. Importantly, our results indicate that any long-term (weeks to months net offsets in reef-water pCO(2 relative to offshore values should be modest for reef systems with narrow and/or deep lagoons. Thus, the long-term evolution of water column pCO(2 in many reef environments remains intimately connected to the regional-scale oceanography of offshore waters and hence directly influenced by rapid anthropogenically driven increases in pCO(2.

  20. RETENTION OF HUMIC ACID FROM WATER BY NANOFILTRATION MEMBRANE AND INFLUENCE OF SOLUTION CHEMISTRY ON MEMBRANE PERFORMANCE

    Directory of Open Access Journals (Sweden)

    M. A. Zazouli, S. Nasseri, A. H. Mahvi, M. Gholami, A. R. Mesdaghinia, M. Younesian

    2008-01-01

    Full Text Available The objectives of this research were to investigate the rejection efficiency of salt and hydrophobic fraction of natural organic matter, to study the flux decline behavior with a spiral wound nanofiltration membrane, and also to survey the influence of water chemistry on membrane performance. Experiments were conducted using a cross flow pilot-scale membrane unit with a full circulation mode. Humic acid was used as hydrophobic organic matter and NaCl as background electrolyte. Results showed that flux reduction increased with increasing ionic strength and humic acid concentration, and with lower pH. The rejection efficiency of organic and salt decreased with the decrease in pH and increase in ionic strength, because of osmotic pressure increase, leading to permeate flux decline and decrease in salt rejection. In addition, the improved salt rejection was likely due to Donnan exclusion by humic material close to membrane surfaces. The average rejection efficiency of humic acid and salt ranged between 91.2%-95.25% and 63.6%-80%, respectively. Dissolved organic carbon concentration was less than 0.57mg/L in permeate for all experiments. With increasing organic concentration, the charge of the membrane surface has become more negative due to the adsorption of organic foulants on the membrane surface, and thus increased the electrostatic repulsion. However, the increasing surface charge had the potential to result in a larger molecular weight cut-off of a fouled membrane due to membrane swelling which can lead to lower rejection solutes. Therefore, results of this study indicated that membrane fouling may significantly affect the rejection of organic and ion solute.

  1. Effects of low-level radioactive-waste disposal on water chemistry in the unsaturated zone at a site near Sheffield, Illinois, 1982-84

    Science.gov (United States)

    Peters, C.A.; Striegl, R.G.; Mills, P.C.; Healy, R.W.

    1992-01-01

    A 1982-84 field study defined the chemistry of water collected from the unsaturated zone at a low-level radioactive-waste disposal site near Sheffield, Bureau County, Illinois. Chemical data were evaluated to determine the principal naturally occurring geochemical reactions in the unsaturated zone and to evaluate waste-induced effects on pore-water chemistry. Samples of precipitation, unsaturated-zone pore water, and saturated-zone water were analyzed for specific conductance, pH, alkalinity, major cations and anions, dissolved organic carbon, gross alpha and beta radiation, and tritium. Little change in concentration of most major constituents in the unsaturated-zone water was observed with respect to depth or distance from disposal trenches. Tritium and dissolved organic carbon concentrations were, however, dependent on proximity to trenches. The primary reactions, both on- site and off-site, were carbonate and clay dissolution, cation exchange, and the oxidation of pyrite. The major difference between on-site and off-site inorganic water chemistry resulted from the removal of the Roxana Silt and the Radnor Till Member of the Glasford Formation from on-site. Off-site, the Roxana Silt contributed substantial quantities of sodium to solution from montmorillonite dissolution and associated cation-exchange reactions. The Radnor Till Member provided exchange surfaces for magnesium. Precipitation at the site had an ionic composition of calcium zinc sulfate and an average pH of 4.6. Within 0.3 meter of the land surface, infiltrating rain water or snowmelt changed to an ionic canposition of calcium sulfate off-site and calcium bicarbonate on-site and had an average pH of 7.9; below that depth, pH averaged 7.5 and the ionic composition generally was calcium magnesium bicarbonate. Alkalinity and specific conductance differed primarily according to composition of geologic materials. Tritium concentrations ranged from 0.2 (detection limit) to 1,380 nanocuries per liter. The

  2. Water physics and chemistry data from bottle casts from the GERDA as part of the Rosenstiel School of Marine and Atmospheric Science (RSMAS) project from 20 July 1955 to 29 May 1957 (NODC Accession 7000057)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected from bottle casts from the GERDA from 20 July 1955 to 29 May 1957. Data were collected as part of the Rosenstiel...

  3. Water physics and chemistry data from moored current meter and bottle casts in the New York Bight as part of the North East Monitoring Program (NEMP) project, 10 April 1984 - 31 October 1984 (NODC Accession 8500225)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the New York Bight from April 10, 1984 to October 31, 1984. Data were...

  4. Water physics and chemistry data from XBT casts from the OCEAN PRINCE and other platforms as part of the Ocean Dumping project from 04 December 1976 to 27 October 1977 (NODC Accession 7800049)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected from XBT casts from the OCEAN PRINCE and other platforms from 04 December 1976 to 27 October 1977. Data were...

  5. Water physics and chemistry data from moored current meter and bottle casts in the Gulf of Mexico as part of the Brine Disposal project, 04 December 1979 - 11 June 1980 (NODC Accession 8000476)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Gulf of Mexico from December 4, 1979 to June 11, 1980. Data were...

  6. Water physics and chemistry data from moored current meter and bottle casts in the Northwest Atlantic Ocean as part of the North East Monitoring Program (NEMP) project, 02 September 1980 - 06 September 1980 (NODC Accession 8100628)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Northwest Atlantic Ocean from September 2, 1980 to September 6,...

  7. Water physics and chemistry data from moored current meter and bottle casts in the Northwest Atlantic Ocean as part of the North East Monitoring Program (NEMP) project, 03 June 1981 - 09 June 1981 (NODC Accession 8100724)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Northwest Atlantic Ocean from June 3, 1981 to June 9, 1981. Data...

  8. Water physics and chemistry data from bottle casts from MULTIPLE SHIPS and other platforms from the NW Atlantic (limit-40 W) from 10 January 1951 to 18 April 1957 (NODC Accession 7200385)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected from bottle casts from MULTIPLE SHIPS and other platforms from NW Atlantic (limit-40 W) from 10 January 1951 to 18...

  9. Water physics and chemistry data from moored current meter and bottle casts in the Northwest Atlantic Ocean as part of the North East Monitoring Program (NEMP) project, 27 July 1982 - 02 August 1982 (NODC Accession 8400002)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Northwest Atlantic Ocean from July 27, 1982 to August 2, 1982....

  10. Water physics and chemistry data from moored current meter and bottle casts in the Northwest Atlantic Ocean as part of the North East Monitoring Program (NEMP) project, 15 April 1981 - 20 April 1981 (NODC Accession 8100656)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Northwest Atlantic Ocean from April 15, 1981 to April 20, 1981....

  11. Water physics and chemistry data from moored current meter and bottle casts in the Northwest Atlantic Ocean as part of the North East Monitoring Program (NEMP) project, 21 April 1980 - 18 July 1980 (NODC Accession 8100501)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Water physics and chemistry data were collected using moored current meter and bottle casts in the Northwest Atlantic Ocean from April 21, 1980 to July 18, 1980....

  12. The influence of fish cage aquaculture on pelagic carbon flow and water chemistry in tidally dominated mangrove estuaries of peninsular Malaysia.

    Science.gov (United States)

    Alongi, D M; Chong, V C; Dixon, P; Sasekumar, A; Tirendi, F

    2003-05-01

    The impact of floating net cages culturing the seabass, Lates calcarifer, on planktonic processes and water chemistry in two heavily used mangrove estuaries in Malaysia was examined. Concentrations of dissolved inorganic and particulate nutrients were usually greater in cage vs. adjacent (approximately 100 m) non-cage waters, although most variability in water-column chemistry related to water depth and tides. There were few consistent differences in plankton abundance, production or respiration between cage and non-cage sites. Rates of primary production were low compared with rates of pelagic mineralization reflecting high suspended loads coupled with large inputs of organic matter from mangrove forests, fishing villages, fish cages, pig farms and other industries within the catchment. Our preliminary sampling did not reveal any large-scale eutrophication due to the cages. A crude estimate of the contribution of fish cage inputs to the estuaries shows that fish cages contribute only approximately 2% of C but greater percentages of N (32-36%) and P (83-99%) to these waters relative to phytoplankton and mangrove inputs. Isolating and detecting impacts of cage culture in such heavily used waterways--a situation typical of most mangrove estuaries in Southeast Asia--are constrained by a background of large, highly variable fluxes of organic material derived from extensive mangrove forests and other human activities.

  13. The chemistry and isotopic composition of waters in the low-enthalpy geothermal system of Cimino-Vico Volcanic District, Italy

    Science.gov (United States)

    Battistel, Maria; Hurwitz, Shaul; Evans, William; Barbieri, Maurizio

    2017-01-01

    Geothermal energy exploration is based in part on interpretation of the chemistry, temperature, and discharge rate of thermal springs. Here we present the major element chemistry and the δD, δ18O, 87Sr/86Sr and δ11B isotopic ratio of groundwater from the low-enthalpy geothermal system near the city of Viterbo in the Cimino-Vico volcanic district of west-Central Italy. The geothermal system hosts many thermal springs and gas vents, but the resource is still unexploited. Water chemistry is controlled by mixing between low salinity,HCO3-rich fresh waters (<24.2°C) flowing in shallow volcanic rocks and SO4-rich thermal waters (25.3°C to 62.2°C) ascending from deep, high permeability Mesozoic limestones. The (equivalent) SO4/Cl (0.01–0.02), Na/Cl (2.82–5.83) and B/Cl ratios (0.02–0.38) of thermal waters differs from the ratios in other geothermal systems from Central Italy, probably implying a lack of hydraulic continuity across the region. The δ18O (−6.6‰ to −5.9‰) and δD (−40.60‰ to −36.30‰) isotopic composition of spring water suggest that the recharge area for the geothermal system is the summit region of Mount Cimino. The strontium isotope ratios (87Sr/86Sr) of thermal waters (0.70797–0.70805) are consistent with dissolution of the Mesozoic evaporite-carbonate units that constitute the reservoir, and the ratios of cold fresh waters mainly reflect shallow circulation through the volcanic cover and some minor admixture (<10%) of thermal water as well. The boron isotopic composition (δ11B) of fresh waters (−5.00 and 6.12‰) is similar to that of the volcanic cover, but the δ11B of thermal waters (−8.37‰ to −4.12‰) is a mismatch for the Mesozoic reservoir rocks and instead reflects dissolution of secondary boron minerals during fluid ascent through flysch units that overlie the reservoir. A slow and tortuous ascent enhances extraction of boron but also promotes conductive cooling, partially masking the heat present in the

  14. Spring runoff water-chemistry data from the Standard Mine and Elk Creek, Gunnison County, Colorado, 2010

    Science.gov (United States)

    Manning, Andrew H.; Verplanck, Philip L.; Mast, M. Alisa; Marsik, Joseph; McCleskey, R. Blaine

    2011-01-01

    Water samples were collected approximately every two weeks during the spring of 2010 from the Level 1 portal of the Standard Mine and from two locations on Elk Creek. The objective of the sampling was to: (1) better define the expected range and timing of variations in pH and metal concentrations in Level 1 discharge and Elk Creek during spring runoff; and (2) further evaluate possible mechanisms controlling water quality during spring runoff. Samples were analyzed for major ions, selected trace elements, and stable isotopes of oxygen and hydrogen (oxygen-18 and deuterium). The Level 1 portal sample and one of the Elk Creek samples (EC-CELK1) were collected from the same locations as samples taken in the spring of 2007, allowing comparison between the two different years. Available meteorological and hydrologic data suggest that 2010 was an average water year and 2007 was below average. Field pH and dissolved metal concentrations in Level 1 discharge had the following ranges: pH, 2.90 to 6.23; zinc, 11.2 to 26.5 mg/L; cadmium, 0.084 to 0.158 mg/L; manganese, 3.23 to 10.2 mg/L; lead, 0.0794 to 1.71 mg/L; and copper, 0.0674 to 1.14 mg/L. These ranges were generally similar to those observed in 2007. Metal concentrations near the mouth of Elk Creek (EC-CELK1) were substantially lower than in 2007. Possible explanations include remedial efforts at the Standard Mine site implemented after 2007 and greater dilution due to higher Elk Creek flows in 2010. Temporal patterns in pH and metal concentrations in Level 1 discharge were similar to those observed in 2007, with pH, zinc, cadmium, and manganese concentrations generally decreasing, and lead and copper generally increasing during the snowmelt runoff period. Zinc and cadmium concentrations were inversely correlated with flow and thus apparently dilution-controlled. Lead and copper concentrations were inversely correlated with pH and thus apparently pH-controlled. Zinc, cadmium, and manganese concentrations near the

  15. Colour Chemistry

    Science.gov (United States)

    Griffiths, J.; Rattee, I. D.

    1973-01-01

    Discusses the course offerings in pure color chemistry at two universities and the three main aspects of study: dyestuff chemistry, color measurement, and color application. Indicates that there exists a constant challenge to ingenuity in the subject discipline. (CC)

  16. Chemistry Dashboard

    Science.gov (United States)

    The Chemistry Dashboard is part of a suite of dashboards developed by EPA to help evaluate the safety of chemicals. The Chemistry Dashboard provides access to a variety of information on over 700,000 chemicals currently in use.

  17. Chemistry Notes

    Science.gov (United States)

    School Science Review, 1976

    1976-01-01

    Described are eight chemistry experiments and demonstrations applicable to introductory chemistry courses. Activities include: measure of lattice enthalpy, Le Chatelier's principle, decarboxylation of soap, use of pocket calculators in pH measurement, and making nylon. (SL)

  18. Biophysical chemistry.

    Science.gov (United States)

    Häussinger, Daniel; Pfohl, Thomas

    2010-01-01

    Biophysical chemistry at the Department of Chemistry, University of Basel, covers the NMR analysis of protein-protein interaction using paramagnetic tags and sophisticated microscopy techniques investigating the dynamics of biological matter.

  19. Heterocyclic chemistry

    OpenAIRE

    Hemming, Karl

    2011-01-01

    Recent progress in the synthesis of heterocyclic compounds is presented\\ud 2010 offered highlights in pericyclic chemistry, particularly 1,3-dipolar cycloaddition chemistry, asymmetric synthesis, gold catalysis, organocatalysis, hydroamination, C–H activation and multicomponent reactions.

  20. Combinatorial chemistry

    DEFF Research Database (Denmark)

    Nielsen, John

    1994-01-01

    An overview of combinatorial chemistry is presented. Combinatorial chemistry, sometimes referred to as `irrational drug design,' involves the generation of molecular diversity. The resulting chemical library is then screened for biologically active compounds.......An overview of combinatorial chemistry is presented. Combinatorial chemistry, sometimes referred to as `irrational drug design,' involves the generation of molecular diversity. The resulting chemical library is then screened for biologically active compounds....

  1. Positronium chemistry

    CERN Document Server

    Green, James

    1964-01-01

    Positronium Chemistry focuses on the methodologies, reactions, processes, and transformations involved in positronium chemistry. The publication first offers information on positrons and positronium and experimental methods, including mesonic atoms, angular correlation measurements, annihilation spectra, and statistical errors in delayed coincidence measurements. The text then ponders on positrons in gases and solids. The manuscript takes a look at the theoretical chemistry of positronium and positronium chemistry in gases. Topics include quenching, annihilation spectrum, delayed coincidence

  2. Collaboration Between Environmental Water Chemistry Students and Hazardous Waste Treatment Specialists on the University of Colorado-Boulder Campus

    Science.gov (United States)

    Dittrich, T. M.

    2012-12-01

    semester, the students conduct a bench-scale laboratory exercise where they study part of the treatment process. Several small start-up companies are testing components in the lab, which adds to the colaboration of the project.; Figure 1. Students in Environmental Water Chemistry lab conducting a titration.

  3. Forensic chemistry.

    Science.gov (United States)

    Bell, Suzanne

    2009-01-01

    Forensic chemistry is unique among chemical sciences in that its research, practice, and presentation must meet the needs of both the scientific and the legal communities. As such, forensic chemistry research is applied and derivative by nature and design, and it emphasizes metrology (the science of measurement) and validation. Forensic chemistry has moved away from its analytical roots and is incorporating a broader spectrum of chemical sciences. Existing forensic practices are being revisited as the purview of forensic chemistry extends outward from drug analysis and toxicology into such diverse areas as combustion chemistry, materials science, and pattern evidence.

  4. Removal of Aromatic Pollutant Surrogate from Water by Recyclable Magnetite-Activated Carbon Nanocomposite: An Experiment for General Chemistry

    Science.gov (United States)

    Furlan, Ping Y.; Melcer, Michael E.

    2014-01-01

    A general chemistry laboratory experiment using readily available chemicals is described to introduce college students to an exciting class of nanocomposite materials. In a one-step room temperature synthetic process, magnetite nanoparticles are embedded onto activated carbon matrix. The resultant nanocomposite has been shown to combine the…

  5. Electrochemical Performance of Alloy 690 Under ETA and AVT Water Chemistry Condition%690合金在ETA和AVT水工况下的电化学特性

    Institute of Scientific and Technical Information of China (English)

    朱志平; 赵永福; 周瑜; 郭小翠; 邓奕鹏

    2012-01-01

    采用Tafel极化曲线法和电化学阻抗法研究了690合金在乙醇胺(ETA)和全挥发处理(AVT)两种水工况下的电化学行为,并着重考察了pH值、温度、Cl-和SO42-对690合金电化学性能的影响.结果表明,在两种不同水工况下,pH值升高会提高690合金的耐蚀性,而温度升高和Cl-,SO42-的加入则均会加速690合金的腐蚀.在相同条件下,690合金与ETA水工况有更好的兼容性,ETA的缓蚀性能优于NH3.%The electrochemical corrosion behavior of alloy 690 in environments of ethanolamine(ETA) and all volatile treatment(AVT) water chemistry was studied by means of Tafel polarization curves and electrochemical impedance spectroscopy(EIS) with a particular emphasis on the effect of pH,temperature,Cl-and SO42-on the electrochemical performance of alloy 690.The results showed that under the two different water chemistry conditions,the increase of pH value would enhance the corrosion resistance of the alloy while the elevation of the temperature and the addition Cl-and SO42-would accelerate the corrosion of alloy 690.Under the same conditions,ETA water chemistry environment had a better compatibility with alloy 690 and ETA exhibited better inhibition efficiency than NH3.

  6. Underground water chemistry and the multi varied statistics as a tool for validation of radionuclides origin in underground waters; Quimica de aguas subterraneas e estatistica multivariada como ferramentas para validar a origem de radionuclideos em aguas subterraneas

    Energy Technology Data Exchange (ETDEWEB)

    Lauria, Dejanira C. [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil); Almeida, Rodrigo M.R. de [Universidade Federal Fluminense (UFF), Niteroi, RJ (Brazil). Dept. de Engenharia Civil

    2005-03-15

    Vulnerability assessment to delineate areas that are more susceptible to contamination from anthropogenic sources has become an important element for sensible resource management and land use planning. This paper address a groundwater survey in an area where intensive agricultural activity takes place with the aim of evaluating factors affecting groundwater quality. For this study, 25 samples of ground water were collected from dug wells and major ion concentrations, radioactive isotopes and physic-chemical parameters were determined. As a result of the analysis around 73% of the samples had levels of contaminants, as NO{sub 3}{sup -}, Fe and radioactivity that exceed the maximum contaminant level for tap water. The ground water clustering based on water chemistry pointed out the land fertilization as one of the factors that could be responsible for the water contamination. (author)

  7. Techniques for detecting effects of urban and rural land-use practices on stream-water chemistry in selected watersheds in Texas, Minnesota,and Illinois

    Science.gov (United States)

    Walker, J.F.

    1993-01-01

    Although considerable effort has been expended during the past two decades to control nonpoint-source contamination of streams and lakes in urban and rural watersheds, little has been published on the effectiveness of various management practices at the watershed scale. This report presents a discussion of several parametric and nonparametric statistical techniques for detecting changes in water-chemistry data. The need for reducing the influence of natural variability was recognized and accomplished through the use of regression equations. Traditional analyses have focused on fixed-frequency instantaneous concentration data; this report describes the use of storm load data as an alternative.

  8. Understanding the Atomic-Level Chemistry and Structure of Oxide Deposits on Fuel Rods in Light Water Nuclear Reactors Using First Principles Methods

    Science.gov (United States)

    Rak, Zs.; O'Brien, C. J.; Brenner, D. W.; Andersson, D. A.; Stanek, C. R.

    2016-09-01

    The results of recent studies are discussed in which first principles calculations at the atomic level have been used to expand the thermodynamic database for science-based predictive modeling of the chemistry, composition and structure of unwanted oxides that deposit on the fuel rods in pressurized light water nuclear reactors. Issues discussed include the origin of the particles that make up deposits, the structure and properties of the deposits, and the forms by which boron uptake into the deposits can occur. These first principles approaches have implications for other research areas, such as hydrothermal synthesis and the stability and corrosion resistance of other materials under other extreme conditions.

  9. Thermodynamics of forming water clusters at various temperatures and pressures by Gaussian-2, Gaussian-3, complete basis set-QB3, and complete basis set-APNO model chemistries; implications for atmospheric chemistry.

    Science.gov (United States)

    Dunn, Meghan E; Pokon, Emma K; Shields, George C

    2004-03-03

    The Gaussian-2, Gaussian-3, complete basis set- (CBS-) QB3, and CBS-APNO methods have been used to calculate Delta H degrees and Delta G degrees values for neutral clusters of water, (H(2)O)(n), where n = 2-6. The structures are similar to those determined from experiment and from previous high-level calculations. The thermodynamic calculations by the G2, G3, and CBS-APNO methods compare well against the estimated MP2(CBS) limit. The cyclic pentamer and hexamer structures release the most heat per hydrogen bond formed of any of the clusters. While the cage and prism forms of the hexamer are the lowest energy structures at very low temperatures, as temperature is increased the cyclic structure is favored. The free energies of cluster formation at different temperatures reveal interesting insights, the most striking being that the cyclic trimer, cyclic tetramer, and cyclic pentamer, like the dimer, should be detectable in the lower troposphere. We predict water dimer concentrations of 9 x 10(14) molecules/cm(3), water trimer concentrations of 2.6 x 10(12) molecules/cm(3), tetramer concentrations of approximately 5.8 x 10(11) molecules/cm(3), and pentamer concentrations of approximately 3.5 x 10(10) molecules/cm(3) in saturated air at 298 K. These results have important implications for understanding the gas-phase chemistry of the lower troposphere.

  10. Quality of water and chemistry of bottom sediment in the Rillito Creek basin, Tucson, Arizona, 1992-93

    Science.gov (United States)

    Tadayon, Saeid

    1995-01-01

    Physical and chemical data were collected from four surface-water sites, six ground-water sites, and two bottom-sediment sites during 1992-93. Specific conductance, hardness, alkalinity, and dissolved- solids concentrations generally were higher in ground water than in surface water. The median concentrations of dissolved major ions, with the exception of potassium, were higher in ground water than in surface water. In surface water and ground water, calcium was the dominant cation, and bicarbonate was the dominant anion. Concentrations of dissolved nitrite and nitrite plus nitrate in surface water and ground water did not exceed the U.S. Environmental Protection Agency maximum contaminant levels of 1 and 10 milligrams per liter for drinking water, respectively. Ammonium plus organic nitrogen in bottom sediment was detected at the highest concentration of any nitrogen species. Median values for most of the dissolved trace elements in surface water and ground water were below the detection levels. Dissolved trace elements in surface water and ground water did not exceed the U.S. Environmental Protection Agency maximum contaminant levels for drinking water. Trace-element concentrations in bottom sediment were similar to trace-element concentrations reported for soils of the western conterminous United States. Several organochlorine pesticides and priority pollutants were detected in surface-water and bottom-sediment samples; however, they did not exceed water-quality standards. Pesticides or priority pollutants were not detected in ground-water samples.

  11. Oskarshamn site investigation. Hydrogeochemical monitoring programme for core and percussion drilled boreholes 2009. Summary of ground water chemistry results from spring and autumn sampling

    Energy Technology Data Exchange (ETDEWEB)

    Regander, Claes; Bergman, Bo (Sweco Environment AB (Sweden))

    2010-09-15

    This report summarises the results obtained in 2009 from the hydrogeochemical monitoring programme for core and percussion drilled boreholes. During 2009 groundwater sampling has been performed in monitored (permanently installed) boreholes in two sampling periods, spring (May-June), and autumn (October-November). Both in spring and autumn groundwater sampling was carried out in the following 12 sections; HLX28:2, HLX35:2, HLX37:1, HLX39:1, KLX08:4, KLX10:2, KLX10:5, KLX12A:2, KLX15A:3, KLX15A:6, KLX18A:3, KLX19A:3. The programme started in 2005 and since then water sampling has been performed twice every year. The objective of the hydrogeochemical monitoring programme is to determine the groundwater composition in selected sections chosen for this purpose. In 2009 the sampling of core drilled borehole sections has been conducted in time series, where each borehole section has been sampled at seven occasions. Percussion drilled borehole sections has been sampled at three occasions. The final sample in each section was taken when the electric conductivity had reached a stable level. Obtained results from the activities presented here include groundwater chemistry data in accordance with SKB chemistry class 5 including options and SKB chemistry reduced class 5. SKB chemistry reduced class 5 includes analysis of pH, electric conductivity, alkalinity, density, drill water (uranine), major cations (Chapter 5.4), F-, Br-, Cl-, SO{sub 4}2-, Fe(II)/Fe(tot), HS-, DOC, TOC and the isotopes delta2H, delta18O and 3H. Options for SKB chemistry class 5 include even lanthanoids and other trace elements, As, In, I, environmental metals, NH{sub 4}+, nutrient salts and the isotopes delta34S, delta37Cl, 87Sr/86Sr, 10B/11B, delta13C, 226Ra, 222Rn, 238U, 234U, 230Th and 232Th. All data from the activity are stored in the SICADA database

  12. Questa baseline and pre-mining ground-water quality investigation. 20. Water chemistry of the Red River and selected seeps, tributaries, and precipitation, Taos County, New Mexico, 2000-2004

    Science.gov (United States)

    Verplanck, P.L.; McCleskey, R.B.; Nordstrom, D.K.

    2006-01-01

    As part of a multi-year project to infer the pre-mining ground-water quality at Molycorp's Questa mine site, surface-water samples of the Red River, some of its tributaries, seeps, and snow samples were collected for analysis of inorganic solutes and of water and sulfate stable isotopes in selected samples. The primary aim of this study was to document diel, storm event, and seasonal variations in water chemistry for the Red River and similar variations in water chemistry for Straight Creek, a natural analog site similar in topography, hydrology, and geology to the mine site for inferring pre-mining water-quality conditions. Red River water samples collected between 2000 and 2004 show that the largest variations in water chemistry occur during late summer rainstorms, often monsoonal in nature. Within hours, discharge of the Red River increased from 8 to 102 cubic feet per second and pH decreased from 7.80 to 4.83. The highest concentrations of metals (iron, aluminum, zinc, manganese) and sulfate also occur during such events. Low-pH and high-solute concentrations during rainstorm runoff are derived primarily from alteration 'scar' areas of naturally high mineralization combined with steep topography that exposes continually altered rock because erosion is too rapid for vegetative growth. The year 2002 was one of the driest on record, and Red River discharge reflected the low seasonal snow pack. No snowmelt peak appeared in the hydrograph record, and a late summer storm produced the highest flow for the year. Snowmelt was closer to normal during 2003 and demonstrated the dilution effect of snowmelt on water chemistry. Two diel sampling events were conducted for the Red River, one during low flow and the other during high flow, at two locations, at the Red River gaging station and just upstream from Molycorp's mill site. No discernible diel trends were observed except for dissolved zinc and manganese at the upstream site during low flow. Straight Creek drainage water

  13. Aquatic Plant Control Research Program. Effects of Water Chemistry on Aquatic Plants. Growth and Photosynthesis of Myriophyllum spicatum L.

    Science.gov (United States)

    1986-05-01

    A D-A±69 98 AQUATIC PLANT CONTROL RESEARCH PRGRAM EFFECTS OF N*TER 1 I CHEMISTRY ON AQUA .(U) ARMY ENGINEER NATERNAYS I EXPERIMENT STATION VICKSBURG...photosynthesis should be clearly resolved. Objective and Scope 6. The objective of this report is to evaluate the effects of major cation and inorganic...carbon levels on the growth and photosynthesis of M. spicaturn. A secondary objective is to evaluate the relationship between growth and

  14. Computational chemistry

    OpenAIRE

    2000-01-01

    Computational chemistry has come of age. With significant strides in computer hardware and software over the last few decades, computational chemistry has achieved full partnership with theory and experiment as a tool for understanding and predicting the behavior of a broad range of chemical, physical, and biological phenomena. The Nobel Prize award to John Pople and Walter Kohn in 1998 highlighted the importance of these advances in computational chemistry. With massively parallel computers ...

  15. Organic chemistry

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2003-08-15

    This book with sixteen chapter explains organic chemistry on linkage isomerism such as alkane, cycloalkane, alkene, aromatic compounds, stereo selective isomerization, aromatic compounds, stereo selective isomerization, organic compounds, stereo selective isomerization, organic halogen compound, alcohol, ether, aldehyde and ketone, carboxylic acid, dicarboxylic acid, fat and detergent, amino, carbohydrate, amino acid and protein, nucleotide and nucleic acid and spectroscopy, a polymer and medical chemistry. Each chapter has introduction structure and characteristic and using of organic chemistry.

  16. Bioinorganic Chemistry

    OpenAIRE

    Bertini, Ivano; Gray, Harry B.; Lippard, Stephen J.; Valentine, Joan Selverstone

    1994-01-01

    This book covers material that could be included in a one-quarter or one-semester course in bioinorganic chemistry for graduate students and advanced undergraduate students in chemistry or biochemistry. We believe that such a course should provide students with the background required to follow the research literature in the field. The topics were chosen to represent those areas of bioinorganic chemistry that are mature enough for textbook presentation. Although each chapter presents material...

  17. Effects of hydrogen water chemistry on corrosion fatigue behavior of cold-worked 304L stainless steel in simulated BWR coolant environments

    Energy Technology Data Exchange (ETDEWEB)

    Chiang, M.F., E-mail: mfchiang@iner.gov.tw [Institute of Nuclear Energy Research, Division of Nuclear Fuels and Materials, Lungtan, Taoyuan 325, Taiwan (China); Young, M.C.; Huang, J.Y. [Institute of Nuclear Energy Research, Division of Nuclear Fuels and Materials, Lungtan, Taoyuan 325, Taiwan (China)

    2011-04-15

    Corrosion fatigue behavior of stainless steel 304L (SS304L) in a simulated BWR coolant with hydrogen injection was investigated. Hydrogen water chemistry slightly mitigated the corrosion fatigue degradation of the as-received SS304L specimens, but, on the contrary, it slightly increased the corrosion fatigue crack growth rates (CFCGRs) of the cold-worked specimens. All the CFCGR-tested specimens showed similar fracture features, except for the amounts of deposited corrosion debris. The results indicated that decreasing the oxygen concentration of water environment is not an effective measure to suppress the fatigue crack growth rate of cold-worked SS304L. The CFCGRs of the SS304L were determined by an interaction between corrosion, oxide-induced crack closure and cold work in corrosive environments. At a specific level of reduction, cold work could enhance the corrosion fatigue resistance of SS304 both in the air-saturated and HWC coolant environments.

  18. Effects of hydrogen water chemistry on corrosion fatigue behavior of cold-worked 304L stainless steel in simulated BWR coolant environments

    Science.gov (United States)

    Chiang, M. F.; Young, M. C.; Huang, J. Y.

    2011-04-01

    Corrosion fatigue behavior of stainless steel 304L (SS304L) in a simulated BWR coolant with hydrogen injection was investigated. Hydrogen water chemistry slightly mitigated the corrosion fatigue degradation of the as-received SS304L specimens, but, on the contrary, it slightly increased the corrosion fatigue crack growth rates (CFCGRs) of the cold-worked specimens. All the CFCGR-tested specimens showed similar fracture features, except for the amounts of deposited corrosion debris. The results indicated that decreasing the oxygen concentration of water environment is not an effective measure to suppress the fatigue crack growth rate of cold-worked SS304L. The CFCGRs of the SS304L were determined by an interaction between corrosion, oxide-induced crack closure and cold work in corrosive environments. At a specific level of reduction, cold work could enhance the corrosion fatigue resistance of SS304 both in the air-saturated and HWC coolant environments.

  19. Chemistry Technology

    Data.gov (United States)

    Federal Laboratory Consortium — Chemistry technology experts at NCATS engage in a variety of innovative translational research activities, including:Design of bioactive small molecules.Development...

  20. Effect of nitrogen and water treatment on leaf chemistry in horsenettle (Solanum carolinense), and relationship to herbivory by flea beetles (Epitrix spp.) and tobacco hornworm (Manduca sexta).

    Science.gov (United States)

    Cipollini, Martin L; Paulk, Eric; Cipollini, Donald F

    2002-12-01

    We studied the interaction between plants (horsenettle; Solanum carolinense) and herbivorous insects (flea beetles; Epitrix spp., and tobacco hornworm; Manduca sexta) by focusing on three questions: (1) Does variation in nitrogen availability affect leaf chemistry as predicted by the carbon-nutrient balance (CNB) hypothesis? (2) Does variation in plant treatment and leaf chemistry affect insect feeding? (3) Is there an interaction between the insect herbivores that is mediated by variation in leaf chemistry? For three successive years (1998-2001), we grew a set of clones of 10 maternal plants under two nitrogen treatments and two water treatments. For each plant in the summer of 2000, we assayed herbivory by hornworms in both indoor (detached leaf) and outdoor (attached leaf) assays, as well as ambient flea beetle damage. Estimates of leaf material consumed were made via analysis of digitized leaf images. We also assayed leaves for total protein, phenolic, and glycoalkaloid content, and for trypsin inhibitor, polyphenol oxidase, and peroxidase activity. Despite strong effects of nitrogen treatment on growth and reproduction, only total protein responded as predicted by CNB. Leaf phenolic levels were increased by nitrogen treatment, polyphenol oxidase activity was decreased, and other leaf parameters were unaffected. Neither hornworm nor flea beetle herbivory could be related to plant treatment or genotype or to variation in any of the six leaf chemical parameters. A negative relationship between flea beetle and hornworm herbivory was found, but was not apparently mediated by any of the measured leaf chemicals. Because leaf resistance was maintained in low nitrogen plants at the apparent expense of growth and reproduction, our results support the concept of a fitness cost of defense, as predicted by the optimal defense hypothesis.

  1. Chemistry and origin of deep ground water in crystalline rocks; Kemi och genes av djupa grundvatten i kristallint berg

    Energy Technology Data Exchange (ETDEWEB)

    Lagerblad, B. [Swedish Cement and Concrete Research Inst., Stockholm (Sweden)

    1995-11-01

    This report discusses the interactions between water and crystalline rocks and its consequences for the chemical composition of the water. It also treats how flows of different types of water are modified by the rock, and the possible consequences for the ground water near a nuclear waste repository. The focus of the work is the changes in composition that ground water gets at deep levels in the rock. Data from Finnsjoen and Aespoe in Sweden show higher salinity in deep rock, which has been interpreted as a result of marine inflow of water during glaciation. Data from other, deeper boreholes in Finland, Canada, Russia, England and Sweden show that the increasing salinity is a rule and very high at great depths, higher than marine water can produce. Therefore, the deep waters from Finnsjoen and Aespoe are probably very old, and the high salinity a result from geological processes. Differing cation and isotopic composition than seawater also indicate geologic water. Differing theories on the origin of the ground water should be regarded in the safety analysis for a repository. 36 refs, 3 figs, 1 tab.

  2. Evaluation of groundwater chemistry and its impact on drinking and irrigation water quality in the eastern part of the Central Arabian graben and trough system, Saudi Arabia

    Science.gov (United States)

    Zaidi, Faisal K.; Mogren, Saad; Mukhopadhyay, Manoj; Ibrahim, Elkhedr

    2016-08-01

    The present study deals with the assessment of groundwater with respect to the main hydrological processes controlling its chemistry and its subsequent impact on groundwater quality for drinking and irrigation purposes in the eastern part of the Central Arabian graben and trough system. Groundwater samples were collected from 73 bore wells tapping the Cretaceous Biyadh and Wasia sandstone aquifers. The main groundwater facies in the area belong to the mixed Casbnd Mgsbnd SO4/Cl type and the SO4sbnd Cl type. Prolonged rock water interaction has resulted in high TDS (average of 2131 mg/l) and high EC (average of 2725 μS/cm) of the groundwater. The average nitrate (56.38 mg/l) value in the area is higher than the WHO prescribed limits of 50 mg/l in drinking water and is attributed to agricultural activities. The Drinking Water Quality Index (DWQI) shows that 33% of the water samples fall within the excellent to good category whereas the remaining samples fall in the poor to unsuitable for drinking category. In terms of Sodium Adsorption Ratio (SAR), Sodium percentage (Na %) and Residual Sodium Carbonate (RSC) the groundwater is suitable for irrigation however the high salinity values can adversely affect the plant physiology.

  3. Strontium isotope ({sup 87}SR/{sup 86}SR) chemistry in produced oilfield waters : the IEA Weyburn CO{sub 2} Monitoring and Storage Project

    Energy Technology Data Exchange (ETDEWEB)

    Quattrocchi, F.; Bencini, R.; Cinti, D.; Galli, G.; Pizzino, L.; Voltattorni, N. [Istituto Nazionale di Geofisica e Vulcanologia, Rome (Italy); Barbieri, M. [La Sapienza Univ., Rome (Italy). IGAG-CNR; Durocher, K.; Shevalier, M. [Calgary Univ., AB (Canada). Dept. of Geology and Geophysics; Gunter, W.D.; Perkins, E.H. [Alberta Research Council, Edmonton, AB (Canada)

    2005-07-01

    A water-alternating-gas (WAG) enhanced oil recovery (EOR) technique is used at the Weyburn Field in southern Saskatchewan, the site of an international project on carbon sequestration. Carbon dioxide (CO{sub 2}) and water are injected into the Midale Formation of the Weyburn Field. In 2001, Italy's Istituto Nazionale di Geofisica e Vulcanologia (INGV) conducted geochemical monitoring of the Weyburn Field oil waters in conjunction with the University of Calgary and the Alberta Research Council. In addition to the main chemistry and gas chemistry, approximately 25 strontium isotopic ratios ({sup 87}Sr/{sup 86}Sr) were analysed in order to improve the knowledge about the CO{sub 2} storage potential. The main reason for monitoring produced fluid and gas isotopes is to quantify water-gas-rock reactions in the reservoir and to better predict the long-term storage of CO{sub 2} in the subsurface. This paper described in detail the methodology used to measure the {sup 87}Sr/{sup 86}Sr ratio. The areas characterized by lowest values of the Sr isotopic ratio represented contamination zones of Mississippian Midale fluids by re-injected Mannville make-up water. These zones had lower Sr isotopic values that coincided with the highest injection volumes of Cretaceous water used for industrial flooding. Concurrently, the average field-wide {sup 87}Sr/{sup 86}Sr values were approaching Mississippian host-rock values, pointing towards areas of the field characterized by higher carbonate dissolution, as a result of continue CO{sub 2} injection. Both injected CO{sub 2} and carbonate mineral dissolution in the reservoir have been traced. Injected CO{sub 2} has a distinctive {delta}{sup 13}C signature of -21 per cent, a value that remained stable through 2 years of up to 10 per cent CO{sub 2} recycling. Therefore, the second strontium isotope scenario fits well with the {delta}{sup 13}C data. The Sr isotopic ratio in produced fluids increases with time, indicating input from

  4. Determination of concentration of radon, volatile organic compounds (VOC) and water chemistry in springs near to Popocatepetl volcano; Determinacion de la concentracion de radon, VOCs y Quimica del agua en manantiales cercanos al volcan Popocatepetl

    Energy Technology Data Exchange (ETDEWEB)

    Pena, P.; Segovia, N.; Lopez M, B.E.; Cisniega, G. [ININ, A.P. 18-1027, 11801 Mexico D.F. (Mexico); Valdes, C.; Armienta, M.A.; Mena, M. [Instituto de Geofisica, UNAM, 04510 Mexico D.F. (Mexico)

    2004-07-01

    Popocatepetl volcano is a high-risk active volcano in Central Mexico where the highest population density in the country is settled. Radon in the soil and groundwater together with water chemistry from samples of nearby springs is analysed as a function of the 2002-2003 volcanic activity. Soil radon indicated fluctuations related both the meteorological parameters and sporadic explosive events. Groundwater radon showed essentially differences in concentration due to the specific characteristics of the studied springs. Water chemistry showed stability along the monitoring period indicating also differences between springs. No anthropogenic pollution from volatile organic compounds was observed. (Author)

  5. Chemistry and dissolved gases of matrix pore water and fluid inclusions in Olkiluoto bedrock from drillhole ONK-PH9

    Energy Technology Data Exchange (ETDEWEB)

    Eichinger, F.; Haemmerli, J.; Waber, H.N.; Diamond, L.W. [Univ. of Bern (Switzerland). Inst. of Geological Sciences; Smellie, J.A.T. [Conterra AB, Stockholm (Sweden)

    2013-05-15

    Matrix pore water and gas dissolved in matrix pore water in drillcore samples from drillhole ONK-PH9 have been successfully characterised for their chemical and isotopic composition. Based on the comparison of natural tracers in matrix pore water and adjacent fracture groundwater, conclusions about the palaeohydrogeological history of the encountered system are drawn. The investigations are based on naturally saturated core samples from the subhorizontal drillhole ONK-PH9 which was drilled from the ONKALO access tunnel at a vertical depth of 306 m into the bedrock intersecting the water-conducting hydrogeological zone HZ20B. Pore water samples were taken from this highly transmissive water-conducting zone and the adjacent low transmissive bedrock along a continuous eleven metre long profile. Additional samples have been collected at intervals between five and ten metres until 100 m drillhole length (DHL)

  6. Influence of drainage status on soil and water chemistry, litter decomposition and soil respiration in central Amazonian forests on sandy soils

    Directory of Open Access Journals (Sweden)

    Antônio Ocimar Manzi

    2011-04-01

    Full Text Available Central Amazonian rainforest landscape supports a mosaic of tall terra firme rainforest and ecotone campinarana, riparian and campina forests, reflecting topography-induced variations in soil, nutrient and drainage conditions. Spatial and temporal variations in litter decomposition, soil and groundwater chemistry and soil CO2 respiration were studied in forests on sandy soils, whereas drought sensitivity of poorly-drained valley soils was investigated in an artificial drainage experiment. Slightly changes in litter decomposition or water chemistry were observed as a consequence of artificial drainage. Riparian plots did experience higher litter decomposition rates than campina forest. In response to a permanent lowering of the groundwater level from 0.1 m to 0.3 m depth in the drainage plot, topsoil carbon and nitrogen contents decreased substantially. Soil CO2 respiration decreased from 3.7±0.6 µmol m-2 s-1 before drainage to 2.5±0.2 and 0.8±0.1 µmol m-2 s-1 eight and 11 months after drainage, respectively. Soil respiration in the control plot remained constant at 3.7±0.6 µmol m-2 s-1. The above suggests that more frequent droughts may affect topsoil carbon and nitrogen content and soil respiration rates in the riparian ecosystem, and may induce a transition to less diverse campinarana or short-statured campina forest that covers areas with strongly-leached sandy soil.

  7. Water chemistry and dissolved organic carbon trends in lakes from Canada's Atlantic Provinces: no recovery from acidification measured after 25 years of lake monitoring

    Energy Technology Data Exchange (ETDEWEB)

    Clair, Thomas A.; Dennis, Ian F.; Vet, Robert

    2011-04-15

    In North America industries emitting sulphur oxides have caused acid precipitation leading to modifications in water chemistry conditions. Atlantic Canada is seriously affected by this problem because of its poorly buffering soils and bedrock. Previous studies were conducted showing that compared to other regions of the world, Atlantic Canada's lakes do not have the same chemical trends; thus the aim of this study was to re-analyse Atlantic Canada's lake chemistry with additional data to see if it was changing. This research was carried out on 91 acid sensitive lakes situated in Nova Scotia and Newfoundland with data collected from 1983 to 2007. Results showed an increase in ANCc over the first years despite a decrease in acid deposition and no increase of pH and base cations detected in the lakes. This study showed an increase in Gran titration ANC in the last years which they correlated to a regional increase in annual air temperatures.

  8. An alternative chemistry for both operational and layup protection of high-pressure steam-water cycles using an organic filming amine

    Energy Technology Data Exchange (ETDEWEB)

    Verib, George J. [FirstEnergy Corp., Akron, OH (United States)

    2011-05-15

    Current economic conditions have caused many fossil-fired units to cycle load where previous operation had been a constant-load operation. At best, this operation has become a low-load, or minimum-load, operation during off electric demand periods and full-load operation during peak-load periods. At the most demanding times, the operation of these units has been a daily startup-shutdown situation. Current cycle chemistry guidelines have not minimized corrosion and have not provided protection of unit equipment during economic reserve off periods. Current unit protection strategies are limited since the units must be operationally ready if called upon to generate. The FirstEnergy Corp. has been using an alternative proprietary, organic filming amine to protect units during operation and short-term non-operational periods. This proprietary chemistry has shown the ability to successfully and significantly reduce corrosion throughout the steam-water cycle during transient load situations and during non-operational periods. (orig.)

  9. Characterizing interactions between surface water and groundwater in the Jialu River basin using major ion chemistry and stable isotopes

    Directory of Open Access Journals (Sweden)

    L. Yang

    2012-05-01

    Full Text Available The Jialu River, a secondary tributary of the Huaihe River, has been severely contaminated for the major contaminant sources, such as a number of untreated or lightly treated sewage wastes in some cities. Groundwater along the river is not an isolated component of the hydrologic system, but instead connected with the surface water. This study aims to characterize the relationships between surface water (e.g. reservoirs, lakes and rivers and groundwater near the river in the shallow Quaternary aquifer. The concentration of Cl in North Zhengzhou City increased prominently due to the discharge of a large amount of domestic water. Nitrate and potassium show maximum concentrations in groundwater in Fugou County. These high levels can be attributed to the use of a large quantity of fertilizer over this region. The regional well had water with a constant stable isotopic signature, which illustrates that the groundwater never or rarely receive recharge from surface water. However, the groundwater of transitional well (location SY3 seemed to be recharged by river water via bank infiltration in September 2010. Fractional contributions of river water to the groundwater were calculated based on isotopic and chemical data using a mass-balance approach. Results show that the groundwater was approximately composed of 60–70% river water. These findings would be useful for a better understanding of hydrogeological processes at the river-aquifer interface and ultimately benefit water management in the future.

  10. Quantum chemistry

    CERN Document Server

    Lowe, John P

    1993-01-01

    Praised for its appealing writing style and clear pedagogy, Lowe's Quantum Chemistry is now available in its Second Edition as a text for senior undergraduate- and graduate-level chemistry students. The book assumes little mathematical or physical sophistication and emphasizes an understanding of the techniques and results of quantum chemistry, thus enabling students to comprehend much of the current chemical literature in which quantum chemical methods or concepts are used as tools. The book begins with a six-chapter introduction of standard one-dimensional systems, the hydrogen atom,

  11. Shallow groundwater and soil chemistry response to 3 years of subsurface drip irrigation using coalbed-methane-produced water

    Energy Technology Data Exchange (ETDEWEB)

    Bern, C. R.; Boehlke, A. R.; Engle, M. A.; Geboy, N. J.; Schroeder, K. T.; Zupancic, J. W.

    2013-10-04

    Disposal of produced waters, pumped to the surface as part of coalbed methane (CBM) development, is a significant environmental issue in the Wyoming portion of the Powder River Basin, USA. High sodium adsorption ratios (SAR) of the waters could degrade agricultural land, especially if directly applied to the soil surface. One method of disposing of CBM water, while deriving beneficial use, is subsurface drip irrigation (SDI), where acidified CBM waters are applied to alfalfa fields year-round via tubing buried 0.92 m deep. Effects of the method were studied on an alluvial terrace with a relatively shallow depth to water table (~3 m). Excess irrigation water caused the water table to rise, even temporarily reaching the depth of drip tubing. The rise corresponded to increased salinity in some monitoring wells. Three factors appeared to drive increased groundwater salinity: (1) CBM solutes, concentrated by evapotranspiration; (2) gypsum dissolution, apparently enhanced by cation exchange; and (3) dissolution of native Na–Mg–SO{sub 4} salts more soluble than gypsum. Irrigation with high SAR (24) water has increased soil saturated paste SAR up to 15 near the drip tubing. Importantly though, little change in SAR has occurred at the surface.

  12. Nutrient sampling slam: high resolution surface-water sampling in streams reveals patterns in groundwater chemistry and flow paths

    Science.gov (United States)

    The groundwater–surface water interface (GSWI), consisting of shallow groundwater adjacent to stream channels, is a hot spot for nitrogen removal processes, a storage zone for other solutes, and a target for restoration activities. Characterizing groundwater-surface water intera...

  13. Shallow groundwater and soil chemistry response to 3 years of subsurface drip irrigation using coalbed-methane-produced water

    Science.gov (United States)

    Bern, Carleton R.; Boehlke, Adam R.; Engle, Mark A.; Geboy, Nicholas J.; Schroeder, K.T.; Zupancic, J.W.

    2013-01-01

    Disposal of produced waters, pumped to the surface as part of coalbed methane (CBM) development, is a significant environmental issue in the Wyoming portion of the Powder River Basin, USA. High sodium adsorption ratios (SAR) of the waters could degrade agricultural land, especially if directly applied to the soil surface. One method of disposing of CBM water, while deriving beneficial use, is subsurface drip irrigation (SDI), where acidified CBM waters are applied to alfalfa fields year-round via tubing buried 0.92 m deep. Effects of the method were studied on an alluvial terrace with a relatively shallow depth to water table (∼3 m). Excess irrigation water caused the water table to rise, even temporarily reaching the depth of drip tubing. The rise corresponded to increased salinity in some monitoring wells. Three factors appeared to drive increased groundwater salinity: (1) CBM solutes, concentrated by evapotranspiration; (2) gypsum dissolution, apparently enhanced by cation exchange; and (3) dissolution of native Na–Mg–SO4 salts more soluble than gypsum. Irrigation with high SAR (∼24) water has increased soil saturated paste SAR up to 15 near the drip tubing. Importantly though, little change in SAR has occurred at the surface.

  14. Water-level fluctuations influence sediment porewater chemistry and methylmercury production in a flood-control reservoir.

    Science.gov (United States)

    Reservoirs typically have elevated fish mercury (Hg) levels compared to natural lakes and rivers. A unique feature of reservoirs is water-level management which can result in sediment exposure to the air. The objective of this study is to identify how reservoir water-level fluct...

  15. Water Chemistry Impacts on Arsenic Mobilization from Arsenopyrite Dissolution and Secondary Mineral Precipitation: Implications for Managed Aquifer Recharge

    Science.gov (United States)

    Managed Aquifer Recharge (MAR) is one water reuse technique with the potential to meet growing water demands. However, MAR sites have encountered arsenic remobilization resulting from recharge operations. To combat this challenge, it is important to identify the mechanism of arse...

  16. The influence of modified water chemistries on metal oxide films, activity build-up and stress corrosion cracking of structural materials in nuclear power plants

    Energy Technology Data Exchange (ETDEWEB)

    Maekelae, K.; Laitinen, T.; Bojinov, M. [VTT Manufacturing Technology, Espoo (Finland)

    1999-03-01

    The primary coolant oxidises the surfaces of construction materials in nuclear power plants. The properties of the oxide films influence significantly the extent of incorporation of actuated corrosion products into the primary circuit surfaces, which may cause additional occupational doses for the maintenance personnel. The physical and chemical properties of the oxide films play also an important role in different forms of corrosion observed in power plants. This report gives a short overview of the factors influencing activity build-up and corrosion phenomena in nuclear power plants. Furthermore, the most recent modifications in the water chemistry to decrease these risks are discussed. A special focus is put on zinc water chemistry, and a preliminary discussion on the mechanism via which zinc influences activity build-up is presented. Even though the exact mechanisms by which zinc acts are not yet known, it is assumed that Zn may block the diffusion paths within the oxide film. This reduces ion transport through the oxide films leading to a reduced rate of oxide growth. Simultaneously the number of available adsorption sites for {sup 60}Co is also reduced. The current models for stress corrosion cracking assume that the anodic and the respective cathodic reactions contributing to crack growth occur partly on or in the oxide films. The rates of these reactions may control the crack propagation rate and therefore, the properties of the oxide films play a crucial role in determining the susceptibility of the material to stress corrosion cracking. Finally, attention is paid also on the novel techniques which can be used to mitigate the susceptibility of construction materials to stress corrosion cracking. (orig.) 127 refs.

  17. Introductory Chemistry

    OpenAIRE

    Baron, Mark; Gonzalez-Rodriguez, Jose; Stevens, Gary; Gray, Nathan; Atherton, Thomas; Winn, Joss

    2010-01-01

    Teaching and Learning resources for the 1st Year Introductory Chemistry course (Forensic Science). 30 credits. These are Open Educational Resources (OER), made available for re-use under a Creative Commons license.

  18. Nuclear Chemistry.

    Science.gov (United States)

    Chemical and Engineering News, 1979

    1979-01-01

    Provides a brief review of the latest developments in nuclear chemistry. Nuclear research today is directed toward increased activity in radiopharmaceuticals and formation of new isotopes by high-energy, heavy-ion collisions. (Author/BB)

  19. Materials Chemistry

    CERN Document Server

    Fahlman, Bradley D

    2011-01-01

    The 2nd edition of Materials Chemistry builds on the strengths that were recognized by a 2008 Textbook Excellence Award from the Text and Academic Authors Association (TAA). Materials Chemistry addresses inorganic-, organic-, and nano-based materials from a structure vs. property treatment, providing a suitable breadth and depth coverage of the rapidly evolving materials field. The 2nd edition continues to offer innovative coverage and practical perspective throughout. After briefly defining materials chemistry and its history, seven chapters discuss solid-state chemistry, metals, semiconducting materials, organic "soft" materials, nanomaterials, and materials characterization. All chapters have been thoroughly updated and expanded with, for example, new sections on ‘soft lithographic’ patterning, ‘click chemistry’ polymerization, nanotoxicity, graphene, as well as many biomaterials applications. The polymer and ‘soft’ materials chapter represents the largest expansion for the 2nd edition. Each ch...

  20. Photocatalytic Treatment of Desalination Concentrate Using Optical Fibers Coated With Nanostructured Thin Films: Impact of Water Chemistry and Seasonal Climate Variations.

    Science.gov (United States)

    Lin, Lu; Wang, Huiyao; Luo, Hongmei; Xu, Pei

    2016-05-01

    Treatment of desalination concentrate can reduce concentrate volume for disposal, increase water recovery and convert waste to resource. However, concentrate treatment is costly and energy intensive due to high concentrations of salt and recalcitrant organic matter in concentrate. Photocatalytic oxidation provides a novel energy neutral technology for concentrate treatment by degrading organic contaminants. Polymer-assisted hydrothermal deposition method was used to synthesize innovative pure and Fe-doped TiO2 mixed-phase nanocomposite thin films on side-glowing optical fibers (SOFs). The properties of the photocatalysts-coated SOF were characterized by surface morphology, nanostructure, crystallite size and phase and zeta potential. Photodegradation efficiency and durability of the photocatalysts treating different types of desalination concentrate was studied under natural sunlight. Synthetic solutions and reverse osmosis (RO) concentrates from brackish water and municipal wastewater desalination facilities were tested to elucidate the impact of water chemistry, operating conditions and seasonal climate variations (solar irradiation intensity and temperature) on photocatalytic efficiency. High ionic strength and divalent electrolyte ions in RO concentrate accelerated photocatalytic process, whereas the presence of carbonate species and organic matter hindered photodegradation. Outdoor testing of immobilized continuous-flow photoreactors suggested that the catalyst-coated SOFs can utilize a wide spectrum of natural sunlight and achieved durable photocatalytic performance.

  1. Summit crater lake observations, and the location, chemistry, and pH of water samples near Mount Chiginagak volcano, Alaska: 2004-2012

    Science.gov (United States)

    Schaefer, Janet R.; Scott, William E.; Evans, William C.; Wang, Bronwen; McGimsey, Robert G.

    2013-01-01

    maximum depth of 45 m (resulting pH ~2.9), and preventing the annual salmon run in the King Salmon River. A simultaneous release of gas and acidic aerosols from the crater caused widespread vegetation damage along the flow path. Since 2005, we have been monitoring the crater lake water that continues to flow into Mother Goose Lake by collecting surface water samples for major cation and anion analysis, measuring surface-water pH of affected drainages, and photo-documenting the condition of the summit crater lake. This report describes water sampling locations, provides a table of chemistry and pH measurements, and documents the condition of the summit crater between 2004 and 2011. In September 2013, the report was updated with results of water-chemistry samples collected in 2011 and 2012, which were added as an addendum.

  2. Green Chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Collison, Melanie

    2011-05-15

    Green chemistry is the science of chemistry used in a way that will not use or create hazardous substances. Dr. Rui Resendes is working in this field at GreenCentre Canada, an offshoot of PARTEQ Innovations in Kingston, Ontario. GreenCentre's preliminary findings suggest their licensed product {sup S}witchable Solutions{sup ,} featuring 3 classes of solvents and a surfactant, may be useful in bitumen oil sands extraction.

  3. Cluster Chemistry

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    @@ Cansisting of eight scientists from the State Key Laboratory of Physical Chemistry of Solid Surfaces and Xiamen University, this creative research group is devoted to the research of cluster chemistry and creation of nanomaterials.After three-year hard work, the group scored a series of encouraging progresses in synthesis of clusters with special structures, including novel fullerenes, fullerene-like metal cluster compounds as well as other related nanomaterials, and their properties study.

  4. Near shore water chemistry data from Island of Hawaii and Lanai 1988-2011 (NODC Accession 0104398)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Coastal water quality was measured at seven shoreline locations on the west side of the Island of Hawaii and one site on Lanai, Hawaii during 1988-2011. Each...

  5. Groundwater contamination and the relationship between water chemistry and biotic components in a karst system (Bihor Mountains, Romania

    Directory of Open Access Journals (Sweden)

    Laura Epure

    2014-12-01

    Full Text Available The physical and chemical characteristics, microbial contaminat ion, and meiofauna of the Ocoale-Gheţar-Dobreşti karst system (Bihor Mountains, Romania were studied in order to assess the natural water quality by an interdisciplinary study. A total of 60 water samples were collected seasonally from 7 sites. Physico-chemical results showed a typical composition of karst waters, except for one site, where Ca2+ was absent, pH was very low, and the abundance and diversity of meiofauna were highest, demonstrating life support even for the most sensitive animals. No significant chemical pollution was found, but microbial contamination occurred in all samples, according to the national water quality standards of the analyzed springs. The Canonical Correlation Analysis and the Canonical Correspondence Analysis performed showed a strong connection between pH, nitrates and faecal pollution, indicating also a direct connection between microbial contaminants and dissolved oxygen.

  6. Water Planets in the Habitable Zone: Atmospheric Chemistry, Observable Features, and the case of Kepler-62e and -62f

    CERN Document Server

    Kaltenegger, L; Rugheimer, S

    2013-01-01

    Water planets in the habitable zone are expected to have distinct geophysics and geochemistry of their surfaces and atmospheres. We explore these properties motivated by two key questions: whether such planets could provide habitable conditions and whether they exhibit discernable spectral features that distinguish a water planet from a rocky Earth-like planet. We show that the recently discovered planets Kepler-62e and -62f are the first viable candidates for habitable zone water planet. We use these planets as test cases for discussing those differences in detail. We generate atmospheric spectral models and find that potentially habitable water planets show a distinctive spectral fingerprint in transit depending on their position in the habitable zone.

  7. Water quality in the vicinity of Mosquito Creek Lake, Trumbull County, Ohio, in relation to the chemistry of locally occurring oil, natural gas, and brine

    Science.gov (United States)

    Barton, G.J.; Burruss, R.C.; Ryder, R.T.

    1998-01-01

    Environmental samples collected in the Mosquito Creek Lake area were used to characterize water quality in relation to the chemistry of locally occurring oil, natural gas, and brine and to establish baseline water quality. Mosquito Creek Lake (a manmade reservoir) and the shallow bedrock aquifers near the lake are major sources of potable water in central Trumbull County. The city of Warren relies on the lake as a sole source of potable water. Some of the lake bottom may be in direct hydraulic connection with the underlying aquifers. The city of Cortland, along the southeastern shore of the lake, relies on the Cussewago Sandstone aquifer as a sole source of potable water. This aquifer subcrops beneath the glacio-fluvial sediments that underlie the lake. Nearly all residential homes around the lake, with the exception of homes in the city of Cortland, rely on domestic supply wells as a source of potable water. Oil and natural gas exploration and production have been ongoing in the Mosquito Creek Lakearea since the discovery of the historic Mecca Oil Pool in the Mississippian Berea and Cussewago Sandstones in 1860. Since the late 1970' s, the major drilling objective and zone of production is the Lower Silurian Clinton sandstone. The oil and natural gas resources of the Mosquito Creek Lake area, including reservoir pressure, production history, and engineering and abandonment practices are described in this report. The chemical and isotopic characteristics of the historic Mecca oil and natural gas are very different than those of the Clinton sandstone oil and natural gas. Gas chromatograms show that Mecca oil samples are extensively altered by biodegradation, whereas Clinton sandstone oils are not. Extensive alteration of Mecca oil is consistent with their occurrence at very shallow depths (less than 100 ft below land surface) where microbial activity can affect their composition. Also, the carbon-isotope composition of dissolved methane gas from Berea and Cussewago

  8. Double-sided Microfluidic Device for Speciation Analysis of Iron in Water Samples: Towards Greener Analytical Chemistry.

    Science.gov (United States)

    Youngvises, Napaporn; Thanurak, Porapichcha; Chaida, Thanatcha; Jukmunee, Jaroon; Alsuhaimi, Awadh

    2015-01-01

    Microfluidics minimize the amounts of reagents and generate less waste. While microdevices are commonly single-sided, producing a substrate with microchannels on multiple surfaces would increase their usefulness. Herein, a polymethymethacrylate substrate incorporating microchannel structures on two sides was sandwiched between two polydimethylsiloxane sheets to create a multi-analysis device, which was used for the spectrophotometric analysis of the ferrous ion (Fe(2+)) and the ferric ion (Fe(3+)), by utilizing colorimetric detection. To monitor the signals from both channel networks, dual optical sensors were integrated into the system. The linear ranges for Fe(2+) and Fe(3+) analyses were 0.1 - 20 mg L(-1) (R(2) = 0.9988) and 1.0 - 40 mg L(-1) (R(2) = 0.9974), respectively. The detection limits for Fe(2+) and Fe(3+) were 0.1 and 0.5 mg L(-1), respectively. The percent recoveries of Fe(2+) and Fe(3+) were 93.5 - 104.3 with an RSD analytical chemistry applications.

  9. Element concentrations in mosses and surface waters of western Canadian mires relative to precipitation chemistry and hydrology

    Energy Technology Data Exchange (ETDEWEB)

    Malmer, N. (Dept. of Ecology, Plant Ecology, Lund Univ., Lund (SE)); Horton, D.G. (Dept. of Botany, the Univ. of Iowa, Iowa City (US)); Vitt, D.H. (Dept. of Botany, the Univ. of Alberta, Edmonton, Alberta (CA))

    1992-01-01

    Concentrations of N, P, S, Na, K, Mg, Ca, Mn, Fe, Cu, Cd, Zn, Pb, Al, and AIA (acid insoluble ash) in mosses (three Sphagnum species and Tomenthypnum nitens, all hummock species) from a variety of mires, both ombrotrophic and minerotrophic, in the coastal western and central parts of Canada are considered in relation to surface water pH and concentrations of Na{sup +}, K{sup +}, Mg{sup 2+}, Ca{sup 2+}, Cl{sup -}, and SO{sub 4}{sup 2-}. Distinct west-east concentration gradients were present for most elements in both mosses and water, but there were correlations between surface water and moss concentrations only for Ca and Mg. On ombrotrophic sites and sites characterized by poor fen vegetation, wet deposition is the main source of elements in the surface water. On rich fen sites, additional Ca and Mg from surrounding soils change the elemental proportions. We conclude that hydrochemically the limit between poor and rich fen sites is more decisive than between bog and fen. The increase in Ca may give brown mosses a competitive advantage over Sphagnum. Moss concentrations of Na and Mg are the only ones decreasing inland. The constancy or inland increase of moss elemental concentrations may depend on either an increasing atmospheric supply (e.g. Pb), differences in moss growth rates (Especially N, P, and K) or site conditions related to the water regime (e.g. Fe and Al). (au).

  10. A Monte-Carlo step-by-step simulation code of the non-homogeneous chemistry of the radiolysis of water and aqueous solutions. Part I: theoretical framework and implementation.

    Science.gov (United States)

    Plante, Ianik

    2011-08-01

    The importance of the radiolysis of water in irradiation of biological systems has motivated considerable theoretical and experimental work in the radiation chemistry of water and aqueous solutions. In particular, Monte-Carlo simulations of radiation track structure and non-homogeneous chemistry have greatly contributed to the understanding of experimental results in radiation chemistry of heavy ions. Actually, most simulations of the non-homogeneous chemistry are done using the Independent Reaction Time (IRT) method, a very fast technique. The main limitation of the IRT method is that the positions of the radiolytic species are not calculated as a function of time, which is needed to simulate the irradiation of more complex systems. Step-by-step (SBS) methods, which are able to provide such information, have been used only sparsely because these are time consuming in terms of calculation. Recent improvements in computer performance now allow the regular use of the SBS method in radiation chemistry. In the present paper, the first of a series of two, the SBS method is reviewed in detail. To these ends, simulation of diffusion of particles and chemical reactions in aqueous solutions is reviewed, and implementation of the program is discussed. Simulation of model systems is then performed to validate the adequacy of stepwise diffusion and reaction schemes. In the second paper, radiochemical yields of simulated radiation tracks calculated by the SBS program in different conditions of LET, pH, and temperature are compared with results from the IRT program and experimental data.

  11. Reduced European emissions of S and N--effects on air concentrations, deposition and soil water chemistry in Swedish forests.

    Science.gov (United States)

    Pihl Karlsson, Gunilla; Akselsson, Cecilia; Hellsten, Sofie; Karlsson, Per Erik

    2011-12-01

    Changes in sulphur and nitrogen pollution in Swedish forests have been assessed in relation to European emission reductions, based on measurements in the Swedish Throughfall Monitoring Network. Measurements were analysed over 20 years with a focus on the 12-year period 1996 to 2008. Air concentrations of SO(2) and NO(2), have decreased. The SO(4)-deposition has decreased in parallel with the European emission reductions. Soil water SO(4)-concentrations have decreased at most sites but the pH, ANC and inorganic Al-concentrations indicated acidification recovery only at some of the sites. No changes in the bulk deposition of inorganic nitrogen could be demonstrated. Elevated NO(3)-concentrations in the soil water occurred at irregular occasions at some southern sites. Despite considerable air pollution emission reductions in Europe, acidification recovery in Swedish forests soils is slow. Nitrogen deposition to Swedish forests continues at elevated levels that may lead to leaching of nitrate to surface waters.

  12. Linking ground-water age and chemistry data along flow paths: Implications for trends and transformations of nitrate and pesticides

    Science.gov (United States)

    Tesoriero, Anthony J.; Saad, David A.; Burow, Karen R.; Frick, Elizabeth A.; Puckett, Larry J.; Barbash, Jack E.

    2007-10-01

    Tracer-based ground-water ages, along with the concentrations of pesticides, nitrogen species, and other redox-active constituents, were used to evaluate the trends and transformations of agricultural chemicals along flow paths in diverse hydrogeologic settings. A range of conditions affecting the transformation of nitrate and pesticides (e.g., thickness of unsaturated zone, redox conditions) was examined at study sites in Georgia, North Carolina, Wisconsin, and California. Deethylatrazine (DEA), a transformation product of atrazine, was typically present at concentrations higher than those of atrazine at study sites with thick unsaturated zones but not at sites with thin unsaturated zones. Furthermore, the fraction of atrazine plus DEA that was present as DEA did not increase as a function of ground-water age. These findings suggest that atrazine degradation occurs primarily in the unsaturated zone with little or no degradation in the saturated zone. Similar observations were also made for metolachlor and alachlor. The fraction of the initial nitrate concentration found as excess N 2 (N 2 derived from denitrification) increased with ground-water age only at the North Carolina site, where oxic conditions were generally limited to the top 5 m of saturated thickness. Historical trends in fluxes to ground water were evaluated by relating the times of recharge of ground-water samples, estimated using chlorofluorocarbon concentrations, with concentrations of the parent compound at the time of recharge, estimated by summing the molar concentrations of the parent compound and its transformation products in the age-dated sample. Using this approach, nitrate concentrations were estimated to have increased markedly from 1960 to the present at all study sites. Trends in concentrations of atrazine, metolachlor, alachlor, and their degradates were related to the timing of introduction and use of these compounds. Degradates, and to a lesser extent parent compounds, were detected

  13. Nitrogen chemistry in surface waters and wet deposition at high altitude in the Sagarmatha (Mt Everest) National Park.

    Science.gov (United States)

    Balestrini, R.; Polesello, S.; Rusconi, M.

    2012-04-01

    The knowledge of the nitrogen cycle is mainly based on studies conducted in relatively human-altered zones located in the north-western hemisphere. Therefore it is of great interest to identify the limits of natural variations of nitrogen in ecosystems that have not experienced the nitrogen pollution, and have undergone minor alterations from human activities. Among the alpine environments of the world, the region of Mount Everest, is a unique ecosystem with a degree of biodiversity among the highest existing, but characterized by a recognized fragility and low resilience. The extreme climate, the slow growing seasons and the thin soils make this ecosystem very sensitive to any environmental change. A yearly sampling campaign was conducted in the Sagarmatha National Park (Nepal) during the monsoon season in 2008 to collect surface water samples at high elevation from 4300 to 5500 m asl. In addition during 2007 and 2008 the sampling of wet deposition was carried on at 5050 m asl at the Nepal Climate Observatory - Pyramid ABC site. The nitrate concentration in the running waters fell in the lower range of the values reported for comparable environments in Europe. As well, the wet deposition load of nitrogen was remarkable lower than those observed in high elevation areas in Europe and North America. A comparison among running waters, precipitations and small lakes, located in the same area, revealed significant higher nitrate concentrations in running waters compared to the other two matrixes. Conversely, ammonia level resulted higher in the rain compared to surface waters. The spatial and temporal variation of the chemical species in running waters were analyzed taking in account the use of soil in the basins and the hydrological regime.

  14. Influence of water chemistry on the distribution of an acidophilic protozoan in an acid mine drainage system at the abandoned Green Valley coal mine, Indiana, USA

    Energy Technology Data Exchange (ETDEWEB)

    Brake, S.S.; Dannelly, H.K.; Connors, K.A.; Hasiotis, S.T. [Indiana State University, Terre Haute, IN (United States). Dept. of Geography Geology & Anthropology

    2001-07-01

    Euglena mutabilis, a benthic photosynthetic protozoan that intracellularly sequesters Fe, is variably abundant in the main effluent channel that contains acid mine drainage (AMD) discharging from the Green Valley coal mine site in western Indiana. Samples of effluent (pH 3.0-4.6) taken from the main channel and samples of contaminated stream water (pH 3.3 to 8.0) collected from an adjacent stream were analyzed to evaluate the influence of water chemistry on E. mutabilis distribution. E. mutabilis communities were restricted to areas containing unmixed effluent with the thickest (up to 3 mm) benthic communities residing in effluent containing high concentrations of total Fe (up to 12110 mg/l), SO{sub 4}(up to 2940 mg/l), Al (up to 1846 mg/l), and Cl (up to 629 mg/l). Communities were also present, but much less abundant, in areas with effluent containing lower concentrations of these same constituents. In effluent where SO{sub 4} was most highly concentrated, E. mutabilis was largely absent, suggesting that extremely high concentrations of SO{sub 4} may have an adverse effect on this potentially beneficial Fe-mediating, acidophilic protozoan.

  15. Linking local riverbed flow patterns and pore-water chemistry to hydrogeologic and geomorphic features across scales

    Science.gov (United States)

    Ibrahim, T. G.; Thornton, S.; Surridge, B.; Wainwright, J.

    2009-12-01

    The groundwater-surface water interface (GSI) is a critical environmental hotspot, a key area influencing the fate of carbon, nutrients and contaminants of surface and subsurface origin, and a zone of ecological importance. Policy seeking to mitigate issues relating to dissolved contaminants and to improve stream health, increasingly recognizes its significance, particularly in the context of integrated management of streams and aquifers. Techniques assessing riverbed flow and solute patterns are often limited to the local scale. When related to the multi-scale pattern of hydrogeologic and geomorphic features controlling stream, hyporheic and groundwater fluxes, they can improve larger scale predictions of flow and solute behaviour at the GSI. This study develops a conceptual model of riverbed flow and solute patterns, and tests it in a 4th order stream in the UK. It assesses the interaction between large scale subsurface flowpaths, driven by the distribution of bedrock outcrops, and the expansion and closure of alluvial deposits, and small-scale hyporheic flowpaths, driven by riffle-pool sequences. It uses two networks of riverbed mini-piezometers and multi-level samplers: network 1, across fifteen sites in a 7.2 km length of river in unconstrained (open alluvial valley), asymmetric (bedrock outcropping on one bank) and constrained (bedrock on both banks) contexts; and network 2, across six riffle-pool sequences in a 350-m reach, at the transition between asymmetric/unconstrained and constrained contexts. Subsurface flowpaths and stream-water infiltration were deduced by relating vertical exchange fluxes to stream and pore-water patterns of conservative natural tracers. Biogeochemical processes were highlighted using reactive natural tracers. At network 2, measurements of surface water profiles and riverbed coring were also undertaken, and dissolved metal concentrations in the first 15 cm of sediments assessed using gel probes. Network 1 was sampled twice. Monthly

  16. The one-dimensional compression method for extraction of pore water from unsaturated tuff and effects on pore-water chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Higgins, J.D.; Burger, P.A. [Colorado School of Mines, Golden, CO (United States); Yang, L.C. [Geological Survey, Denver, CO (United States)

    1997-12-31

    Study of the hydrologic system at Yucca Mountain, Nevada, requires extraction of pore-water samples from unsaturated tuff bedrock. Two generations of compression cells have been designed and tested for extracting representative, unaltered pore-water samples from unsaturated tuff cores. The one-dimensional compression cell has a maximum compressive stress rating of 552 MPa. Results from 86 tests show that the minimum degree of saturation for successful extraction of pore water was about 14% for non welded tuff and about 61% for densely welded tuff. The high-pressure, one-dimensional compression cell has a maximum compressive stress rating of 827 MPa. Results from 109 tests show that the minimum degree of saturation for successful extraction of pore water was about 7.5% for non welded tuff and about 34% for densely welded tuff. Geochemical analyses show that, in general, there is a decrease in ion concentration of pore waters as extraction pressures increase. Only small changes in pore-water composition occur during the one-dimensional extraction test.

  17. Polymer Chemistry

    Science.gov (United States)

    Williams, Martha; Roberson, Luke; Caraccio, Anne

    2010-01-01

    This viewgraph presentation describes new technologies in polymer and material chemistry that benefits NASA programs and missions. The topics include: 1) What are Polymers?; 2) History of Polymer Chemistry; 3) Composites/Materials Development at KSC; 4) Why Wiring; 5) Next Generation Wiring Materials; 6) Wire System Materials and Integration; 7) Self-Healing Wire Repair; 8) Smart Wiring Summary; 9) Fire and Polymers; 10) Aerogel Technology; 11) Aerogel Composites; 12) Aerogels for Oil Remediation; 13) KSC's Solution; 14) Chemochromic Hydrogen Sensors; 15) STS-130 and 131 Operations; 16) HyperPigment; 17) Antimicrobial Materials; 18) Conductive Inks Formulations for Multiple Applications; and 19) Testing and Processing Equipment.

  18. Dynamical variations in groundwater chemistry influenced by intermittent water delivery at the lower reaches of the Tarim River

    Institute of Scientific and Technical Information of China (English)

    CHENYongjin; CHENYaning; LIUJiazhen; LIWeihong; IJun; XUChangchun

    2005-01-01

    The water of Bosten Lake was released to lower reaches of the Tarim River for 5 times from 2000 to 2002. The changes of total dissolved solid (TDS) and the major ions (SO42-, Cl-, Na-,Ca2+, Mg2- and HCO3- ) were analyzed during this period. It was found out that TDS and the concentrations of the major ions initially and quickly increased and then decreased, but finally increased again. These changes were different at different distances from the river, which indicated that the groundwater changes relied on the distance from the river. In addition, the salt in groundwater was only diluted but not removed by the water. It was suggested that ecological measures should be sought to really promote the quality of the groundwater at the lower reaches of the Tarim River.

  19. A green chemistry of graphene: photochemical reduction towards monolayer graphene sheets and the role of water adlayers.

    Science.gov (United States)

    Li, Xin-Hao; Chen, Jie-Sheng; Wang, Xinchen; Schuster, Manfred E; Schlögl, Robert; Antonietti, Markus

    2012-04-01

    Clean sheets: Stable aqueous dispersions of graphene sheets (GSs) are obtained by exposing graphene oxide to irradiation with light at room temperature, without using any chemical additives. The photochemical reduction method is sustainable and scalable, repairs a majority of defects in the graphene layers, and can be used to fine-tune surface functional groups. Interestingly, the aqueous GS dispersions are stable without any added surfactant. The existence of a water layer that is strongly bound to GS is evidenced.

  20. Environmentally-assisted cracking behaviour in the transition region of an Alloy182/SA 508 Cl.2 dissimilar metal weld joint in simulated boiling water reactor normal water chemistry environment

    Science.gov (United States)

    Seifert, H. P.; Ritter, S.; Shoji, T.; Peng, Q. J.; Takeda, Y.; Lu, Z. P.

    2008-08-01

    The stress corrosion cracking (SCC) and corrosion fatigue behaviour perpendicular and parallel to the fusion line in the transition region between the Alloy 182 Nickel-base weld metal and the adjacent SA 508 Cl.2 low-alloy reactor pressure vessel (RPV) steel of a simulated dissimilar metal weld joint was investigated under boiling water reactor normal water chemistry conditions. A special emphasis was placed to the question whether a fast growing interdendritic SCC crack in the highly susceptible Alloy 182 weld metal can easily cross the fusion line and significantly propagate into the adjacent low-alloy RPV steel. Cessation of interdendritic SCC crack growth was observed in high-purity or sulphate-containing oxygenated water under constant or periodical partial unloading conditions for those parts of the crack front, which reached the fusion line. In chloride containing water, on the other hand, the interdendritic SCC crack in the Alloy 182 weld metal very easily crossed the fusion line and further propagated with a very high rate as a transgranular crack into the heat-affected zone and base metal of the adjacent low-alloy steel. The observed SCC cracking behaviour at the interface correlates excellently with the field experience of such dissimilar metal weld joints, where SCC cracking was usually confined to the Alloy 182 weld metal.

  1. Effect of Agricultural Practices on Hydrology and Water Chemistry in a Small Irrigated Catchment, Yakima River Basin, Washington

    Science.gov (United States)

    McCarthy, Kathleen A.; Johnson, Henry M.

    2009-01-01

    The role of irrigation and artificial drainage in the hydrologic cycle and the transport of solutes in a small agricultural catchment in central Washington's Yakima Valley were explored using hydrologic, chemical, isotopic, age-dating, and mineralogical data from several environmental compartments, including stream water, ground water, overland flow, and streambed pore water. A conceptual understanding of catchment hydrology and solute transport was developed and an inverse end-member mixing analysis was used to further explore the effects of agriculture in this small catchment. The median concentrations of major solutes and nitrates were similar for the single field site and for the catchment outflow site, indicating that the net effects of transport processes for these constituents were similar at both scales. However, concentrations of nutrients were different at the two sites, suggesting that field-scale variations in agricultural practices as well as nearstream and instream biochemical processes are important components of agricultural chemical transformation and transport in this catchment. This work indicates that irrigation coupled with artificial drainage networks may exacerbate the ecological effects of agricultural runoff by increasing direct connectivity between fields and streams and minimizing potentially mitigating effects (denitrification and dilution, for example) of longer subsurface pathways.

  2. Oxidizing dissolution of spent MOX47 fuel subjected to water radiolysis: Solution chemistry and surface characterization by Raman spectroscopy

    Science.gov (United States)

    Jégou, C.; Caraballo, R.; De Bonfils, J.; Broudic, V.; Peuget, S.; Vercouter, T.; Roudil, D.

    2010-04-01

    The mechanisms of oxidizing dissolution of spent MOX fuel (MIMAS TU2®) subjected to water radiolysis were investigated experimentally by leaching spent MOX47 fuel samples in pure water at 25 °C under different oxidizing conditions (with and without external gamma irradiation); the leached surfaces were characterized by Raman spectroscopy. The highly oxidizing conditions resulting from external gamma irradiation significantly increased the concentration of plutonium (Pu(V)) and uranium (U(VI)) compared with a benchmark experiment (without external irradiation). The oxidation behavior of the plutonium-enriched aggregates differed significantly from that of the UO 2 matrix after several months of leaching in water under gamma irradiation. The plutonium in the aggregates appears to limit fuel oxidation. The only secondary phases formed and identified to date by Raman spectroscopy are uranium peroxides that generally precipitate on the surface of the UO 2 grains. Concerning the behavior of plutonium, solution analysis results appear to be compatible with a conventional explanation based on an equilibrium with a Pu(OH) 4(am) phase. The fission product release - considered as a general indicator of matrix alteration - from MOX47 fuel also increases under external gamma irradiation and a change in the leaching mode is observed. Diffusive leaching was clearly identified, coinciding with the rapid onset of steady-state actinide concentrations in the bulk solution.

  3. Environmental control technology survey of selected US strip mining sites. Volume 2A: Ohio: water quality impacts and overburden chemistry of Ohio study site

    Energy Technology Data Exchange (ETDEWEB)

    Bogner, J E; Henricks, J D; Olsen, R D; Schubert, J P; Sobek, A A; Wilkey, M L; Johnson, D O

    1979-05-01

    An intensive study of water, overburden, and coal chemistry was conducted at a large surface mine in Ohio from May 1976 through July 1977. Sampling sites were chosen to include the final mine effluent at the outflow of a large settling pond and chemically-treated drainage from a coal storage pile. Samples were collected semimonthly and analyzed for total dissolved solids, total suspended solids, alkalinity, acidity, sulfate, chloride, and 16 metals. Field measurements included pH, flow rate, dissolved oxygen, and specific conductance. The final effluent, where sampled, generally complied with Office of Surface Mining reclamation standards for pH, iron, and total suspended solids. Comparison of the final effluent with water quality of an unnamed tributary above the mine suggested that elevated values for specific conductance, total dissolved solids, sulfate, calcium, magnesium, manganese, and zinc were attributable to the mine operation. In general, there were observable seasonal variations in flow rates that correlated positively to suspended solids concentrations and negatively to concentrations of dissolved constituents in the final effluent. Drainage from the coal storage pile contained elevated levels of acidity and dissolved metals which were not reduced significantly by the soda ash treatment. The storage pile drainage was diluted, however, by large volumes of alkaline water in the settling pond. Analysis of overburden and coal indicated that the major impact of mine drainage was pyrite oxidation and hydrolysis in the Middle Kittanning Coal and in the Lower Freeport Shale overlying the coal. However, the presence of a calcite-cemented section in the Upper Freeport Sandstone contributed substantial self-neutralizing capacity to the overburden section, resulting in generally alkaline drainage at this site.

  4. Scale-dependent effects of land cover on water physico-chemistry and diatom-based metrics in a major river system, the Adour-Garonne basin (South Western France)

    Energy Technology Data Exchange (ETDEWEB)

    Tudesque, Loïc, E-mail: loic.tudesque@univ-tlse3.fr [CNRS, Université Paul Sabatier, ENFA, UMR5174 EDB (Laboratoire Évolution and Diversité Biologique), 118 route de Narbonne, F-31062 Toulouse (France); Université Toulouse 3 Paul Sabatier, CNRS, UMR5174 EDB, F-31062 Toulouse (France); Tisseuil, Clément [CNRS, Université Paul Sabatier, ENFA, UMR5174 EDB (Laboratoire Évolution and Diversité Biologique), 118 route de Narbonne, F-31062 Toulouse (France); Université Toulouse 3 Paul Sabatier, CNRS, UMR5174 EDB, F-31062 Toulouse (France); Lek, Sovan, E-mail: sovan.lek@univ-tlse3.fr [CNRS, Université Paul Sabatier, ENFA, UMR5174 EDB (Laboratoire Évolution and Diversité Biologique), 118 route de Narbonne, F-31062 Toulouse (France); Université Toulouse 3 Paul Sabatier, CNRS, UMR5174 EDB, F-31062 Toulouse (France)

    2014-01-01

    The scale dependence of ecological phenomena remains a central issue in ecology. Particularly in aquatic ecology, the consideration of the accurate spatial scale in assessing the effects of landscape factors on stream condition is critical. In this context, our study aimed at assessing the relationships between multi-spatial scale land cover patterns and a variety of water quality and diatom metrics measured at the stream reach level. This investigation was conducted in a major European river system, the Adour-Garonne river basin, characterized by a wide range of ecological conditions. Redundancy analysis (RDA) and variance partitioning techniques were used to disentangle the different relationships between land cover, water-chemistry and diatom metrics. Our results revealed a top-down “cascade effect” indirectly linking diatom metrics to land cover patterns through water physico-chemistry, which occurred at the largest spatial scales. In general, the strength of the relationships between land cover, physico-chemistry, and diatoms was shown to increase with the spatial scale, from the local to the basin scale, emphasizing the importance of continuous processes of accumulation throughout the river gradient. Unexpectedly, we established that the influence of land cover on the diatom metric was of primary importance both at the basin and local scale, as a result of discontinuous but not necessarily antagonist processes. The most detailed spatial grain of the Corine land cover classification appeared as the most relevant spatial grain to relate land cover to water chemistry and diatoms. Our findings provide suitable information to improve the implementation of effective diatom-based monitoring programs, especially within the scope of the European Water Framework Directive. - Highlights: •The spatial scale dependence of the “cascade effect” in a river system has been demonstrated. •The strength of the relationships between land cover and diatoms through

  5. The role of water in unconventional in situ energy resource extraction technologies: Chapter 7 in Food, energy, and water: The chemistry connection

    Science.gov (United States)

    Gallegos, Tanya J.; Bern, Carleton R.; Birdwell, Justin E.; Haines, Seth S.; Engle, Mark A.

    2015-01-01

    Global trends toward developing new energy resources from lower grade, larger tonnage deposits that are not generally accessible using “conventional” extraction methods involve variations of subsurface in situ extraction techniques including in situ oil-shale retorting, hydraulic fracturing of petroleum reservoirs, and in situ recovery (ISR) of uranium. Although these methods are economically feasible and perhaps result in a smaller above-ground land-use footprint, there remain uncertainties regarding potential subsurface impacts to groundwater. This chapter provides an overview of the role of water in these technologies and the opportunities and challenges for water reuse and recycling.

  6. Inorganic and organic ground-water chemistry in the Canal Creek area of Aberdeen Proving Ground, Maryland

    Science.gov (United States)

    Lorah, M.M.; Vroblesky, D.A.

    1989-01-01

    Groundwater chemical data were collected from November 1986 through April 1987 in the first phase of a 5-year study to assess the possibility of groundwater contamination in the Canal Creek area of Aberdeen Proving Ground, Maryland. Water samples were collected from 87 observation wells screened in Coastal Plain sediments; 59 samples were collected from the Canal Creek aquifer, 18 from the overlying surficial aquifer, and 10 from the lower confined aquifer. Dissolved solids, chloride, iron, manganese, fluoride, mercury, and chromium are present in concentrations that exceed the Federal maximum contaminant levels for drinking water. Elevated chloride and dissolved-solids concentrations appear to be related from contaminant plumes but also could result from brackish-water intrusion. Excessive concentrations of iron and manganese were the most extensive water quality problems found among the inorganic constituents and are derived from natural dissolution of minerals and oxide coatings in the aquifer sediments. Volatile organic compounds are present in the Canal Creek and surficial aquifers, but samples from the lower confined aquifer do not show any evidence of contamination by inorganic or organic chemicals. The volatile organic contaminants detected in the groundwater and their maximum concentrations (in micrograms/L) include 1,1,2,2- tetrachloroethane (9,000); carbon tetrachloride (480); chloroform (460); 1,1,2-trichloroethane (80); 1,2-dichloroethane (990); 1,1-dichloroethane (3.1); tetrachloroethylene (100); trichloroethylene (1,800); 1,2-trans- dichloroethylene (1,200); 1,1-dichloroethylene (4.4); vinyl chloride (140); benzene (70); and chlorobenzene (39). On the basis of information on past activities in the study area, some sources of the volatile organic compounds include: (1) decontaminants and degreasers; (2) clothing-impregnating operations; (3) the manufacture of impregnite material; (4) the manufacture of tear gas; and (5) fuels used in garages and at

  7. F- and H-Area Seepage Basins Water Treatment System Process Optimization and Alternative Chemistry Ion Exchange/Sorbent Material Screening Clearwell Overflow Study

    Energy Technology Data Exchange (ETDEWEB)

    Serkiz, S.M.

    2000-08-30

    This study investigated alternative ion exchange/sorbent materials and polishing chemistries designed to remove specific radionuclides not removed during the neutralization/precipitation/clarification process.

  8. Water-chemistry data for selected springs, geysers, and streams in Yellowstone National Park, Wyoming, 2006-2008

    Science.gov (United States)

    Ball, James W.; McMleskey, R. Blaine; Nordstrom, D. Kirk

    2010-01-01

    Water analyses are reported for 104 samples collected from numerous thermal and non-thermal features in Yellowstone National Park (YNP) during 2006-2008. Water samples were collected and analyzed for major and trace constituents from 10 areas of YNP including Apollinaris Spring and Nymphy Creek along the Norris-Mammoth corridor, Beryl Spring in Gibbon Canyon, Norris Geyser Basin, Lower Geyser Basin, Crater Hills, the Geyser Springs Group, Nez Perce Creek, Rabbit Creek, the Mud Volcano area, and Washburn Hot Springs. These water samples were collected and analyzed as part of research investigations in YNP on arsenic, antimony, iron, nitrogen, and sulfur redox species in hot springs and overflow drainages, and the occurrence and distribution of dissolved mercury. Most samples were analyzed for major cations and anions, trace metals, redox species of antimony, arsenic, iron, nitrogen, and sulfur, and isotopes of hydrogen and oxygen. Analyses were performed at the sampling site, in an on-site mobile laboratory vehicle, or later in a U.S. Geological Survey laboratory, depending on stability of the constituent and whether it could be preserved effectively. Water samples were filtered and preserved on-site. Water temperature, specific conductance, pH, emf (electromotive force or electrical potential), and dissolved hydrogen sulfide were measured on-site at the time of sampling. Dissolved hydrogen sulfide was measured a few to several hours after sample collection by ion-specific electrode on samples preserved on-site. Acidity was determined by titration, usually within a few days of sample collection. Alkalinity was determined by titration within 1 to 2 weeks of sample collection. Concentrations of thiosulfate and polythionate were determined as soon as possible (generally a few to several hours after sample collection) by ion chromatography in an on-site mobile laboratory vehicle. Total dissolved iron and ferrous iron concentrations often were measured on-site in the

  9. Water-Chemistry Data for Selected Springs, Geysers, and Streams in Yellowstone National Park, Wyoming, 2003-2005

    Science.gov (United States)

    Ball, James W.; McCleskey, R. Blaine; Nordstrom, D. Kirk; Holloway, JoAnn M.

    2008-01-01

    Water analyses are reported for 157 samples collected from numerous hot springs, their overflow drainages, and Lemonade Creek in Yellowstone National Park (YNP) during 2003-2005. Water samples were collected and analyzed for major and trace constituents from ten areas of YNP including Terrace and Beryl Springs in the Gibbon Canyon area, Norris Geyser Basin, the West Nymph Creek thermal area, the area near Nymph Lake, Hazle Lake, and Frying Pan Spring, Lower Geyser Basin, Washburn Hot Springs, Mammoth Hot Springs, Potts Hot Spring Basin, the Sulphur Caldron area, and Lemonade Creek near the Solfatara Trail. These water samples were collected and analyzed as part of research investigations in YNP on arsenic, antimony, and sulfur redox distribution in hot springs and overflow drainages, and the occurrence and distribution of dissolved mercury. Most samples were analyzed for major cations and anions, trace metals, redox species of antimony, arsenic, iron, nitrogen, and sulfur, and isotopes of hydrogen and oxygen. Analyses were performed at the sampling site, in an on-site mobile laboratory vehicle, or later in a U.S. Geological Survey laboratory, depending on stability of the constituent and whether it could be preserved effectively. Water samples were filtered and preserved onsite. Water temperature, specific conductance, pH, Eh (redox potential relative to the Standard Hydrogen Electrode), and dissolved hydrogen sulfide were measured onsite at the time of sampling. Acidity was determined by titration, usually within a few days of sample collection. Alkalinity was determined by titration within 1 to 2 weeks of sample collection. Concentrations of thiosulfate and polythionate were determined as soon as possible (generally minutes to hours after sample collection) by ion chromatography in an on-site mobile laboratory vehicle. Total dissolved-iron and ferrous-iron concentrations often were measured onsite in the mobile laboratory vehicle. Concentrations of dissolved

  10. The effects of cold rolling orientation and water chemistry on stress corrosion cracking behavior of 316L stainless steel in simulated PWR water environments

    Science.gov (United States)

    Chen, Junjie; Lu, Zhanpeng; Xiao, Qian; Ru, Xiangkun; Han, Guangdong; Chen, Zhen; Zhou, Bangxin; Shoji, Tetsuo

    2016-04-01

    Stress corrosion cracking behaviors of one-directionally cold rolled 316L stainless steel specimens in T-L and L-T orientations were investigated in hydrogenated and deaerated PWR primary water environments at 310 °C. Transgranular cracking was observed during the in situ pre-cracking procedure and the crack growth rate was almost not affected by the specimen orientation. Locally intergranular stress corrosion cracks were found on the fracture surfaces of specimens in the hydrogenated PWR water. Extensive intergranular stress corrosion cracks were found on the fracture surfaces of specimens in deaerated PWR water. More extensive cracks were found in specimen T-L orientation with a higher crack growth rate than that in the specimen L-T orientation with a lower crack growth rate. Crack branching phenomenon found in specimen L-T orientation in deaerated PWR water was synergistically affected by the applied stress direction as well as the preferential oxidation path along the elongated grain boundaries, and the latter was dominant.

  11. Smart Cities Will Need Chemistry

    Directory of Open Access Journals (Sweden)

    Alexandru WOINAROSCHY

    2016-06-01

    Full Text Available A smart city is a sustainable and efficient urban centre that provides a high quality of life to its inhabitants through optimal management of its resources. Chemical industry has a key role to play in the sustainable evolution of the smart cities. Additionally, chemistry is at the heart of all modern industries, including electronics, information technology, biotechnology and nano-technology. Chemistry can make the smart cities project more sustainable, more energy efficient and more cost effective. There are six broad critical elements of any smart city: water management systems; infrastructure; transportation; energy; waste management and raw materials consumption. In all these elements chemistry and chemical engineering are deeply involved.

  12. Crystal chemistry of amphiboles: implications for oxygen fugacity and water activity in lithospheric mantle beneath Victoria Land, Antarctica

    Science.gov (United States)

    Bonadiman, C.; Nazzareni, S.; Coltorti, M.; Comodi, P.; Giuli, G.; Faccini, B.

    2014-03-01

    Amphibole is the hydrous metasomatic phase in spinel-bearing mantle xenoliths from Baker Rocks, Northern Victoria Land, Antarctica. It occurs in veins or in disseminated form in spinel lherzolites. Both types derive from reaction between metasomatic melts and the pristine paragenesis of the continental lithospheric mantle beneath Northern Victoria Land. To determine the effective role of water circulation during the metasomatic process and amphibole formation, six amphibole samples were fully characterized. Accurate determination of the site population and the state of dehydrogenation in each of these amphiboles was carried out using single-crystal X-ray diffraction, electron microprobe and secondary ion mass spectroscopy on the same single crystal. The Fe3+/ΣFe ratio was determined by X-ray absorption near edge spectroscopy on amphibole powder. The degree of dehydrogenation determined by SIMS is 0.870-0.994 O3(O2-) a.p.f.u., primary and ascribed to the Ti-oxy component of the amphibole, as indicated by atom site populations; post-crystallization H loss is negligible. Estimates of aH2O (0.014-0.054) were determined from the dehydration equilibrium among end-member components assuming that amphiboles are in equilibrium with the anhydrous peridotitic phases. A difference up to 58 % in determination of aH2O can be introduced if the chemical formula of the amphiboles is calculated based on 23 O a.p.f.u. without knowing the effective amount of dehydrogenation. The oxygen fugacity of the Baker Rocks amphibole-bearing mantle xenoliths calculated based upon the dissociation constant of water (by oxy-amphibole equilibrium) is between -2.52 and -1.32 log units below the fayalite-magnetite-quartz (FMQ) buffer. These results are systematically lower and in a narrow range of values relative to those obtained from anhydrous olivine-orthopyroxene-spinel equilibria ( fO2 between -1.98 and -0.30 log units). A comparative evaluation of the two methods suggests that when amphibole

  13. Water-Chemistry Data for Selected Springs, Geysers, and Streams in Yellowstone National Park, Wyoming, 1999-2000

    Science.gov (United States)

    Ball, James W.; McCleskey, R. Blaine; Nordstrom, D. Kirk; Holloway, JoAnn M.; Verplanck, Philip L.; Sturtevant, Sabin A.

    2002-01-01

    Sixty-seven water analyses are reported for samples collected from 44 hot springs and their overflow drainages and two ambient-temperature acid streams in Yellowstone National Park (YNP) during 1990-2000. Thirty-seven analyses are reported for 1999, 18 for June of 2000, and 12 for September of 2000. These water samples were collected and analyzed as part of research investigations in YNP on microbially mediated sulfur oxidation in stream water, arsenic and sulfur redox speciation in hot springs, and chemical changes in overflow drainages that affect major ions, redox species, and trace elements. Most samples were collected from sources in the Norris Geyser Basin. Two ambient-temperature acidic stream systems, Alluvium and Columbine Creeks and their tributaries in Brimstone Basin, were studied in detail. Analyses were performed at or near the sampling site, in an on-site mobile laboratory truck, or later in a USGS laboratory, depending on stability of the constituent and whether or not it could be preserved effectively. Water temperature, specific conductance, pH, Eh, dissolved oxygen (D.O.), and dissolved H2S were determined on-site at the time of sampling. Alkalinity, acidity, and F were determined within a few days of sample collection by titration with acid, titration with base, and ion-selective electrode or ion chromatography (IC), respectively. Concentrations of S2O3 and SxO6 were determined as soon as possible (minutes to hours later) by IC. Concentrations of Br, Cl, NH4, NO2, NO3, SO4, Fe(II), and Fe(total) were determined within a few days of sample collection. Densities were determined later in the USGS laboratory. Concentrations of Li and K were determined by flame atomic absorption spectrometry. Concentrations of Al, As(total), B, Ba, Be, Ca, Cd, Co, Cr, Cu, Fe(total), K, Li, Mg, Mn, Na, Ni, Pb, Se, Si, Sr, V, and Zn were determined by inductively-coupled plasma-optical emission spectrometry. Trace concentrations of Cd, Cr, Cu, Pb, and Sb were

  14. The water chemistry of some shallow lakes in Northern Patagonia and their nitrogen status in comparison with remote lakes in different regions of the globe

    Directory of Open Access Journals (Sweden)

    Rosario MOSELLO

    2008-08-01

    Full Text Available Eighteen small shallow lakes located in the Northern Patagonian Lake District, in southern South America, were sampled in 2001 and analysed for the main chemical variables (pH, conductivity, alkalinity, major ions and nutrients. The study lakes span a wide geographical and altitudinal range and belong partly to the Pacific and partly to the Atlantic watershed. The main aim of this study was to investigate the relationships between water chemistry and physical/geographical properties of these lakes. Secondly, the nitrogen content of the lakes was considered in detail, and results compared to those obtained in previous studies carried out in other remote areas of the globe (the Central Southern Alps in Italy, the Sierra da Estrela region in Portugal, the Svalbard Islands in the Arctic, the Khumbu-Himal region in Nepal, and the Terra Nova Bay area in Antarctica. In the Alps, lakes are characterised by markedly high nitrogen concentrations, manly as nitrate, due to the high inputs of nitrogen compounds from downwind sources like the Po Plain in Northern Italy. Conversely, lakes at remote locations such as the Andes, Antarctica and Himalaya are characterised by a low nitrogen content, mainly as organic nitrogen. This status is related to the limited atmospheric inputs of nitrogen affecting these regions.

  15. Dragonfly Mercury Project—A citizen science driven approach to linking surface-water chemistry and landscape characteristics to biosentinels on a national scale

    Science.gov (United States)

    Eagles-Smith, Collin A.; Nelson, Sarah J.; Willacker,, James J.; Flanagan Pritz, Colleen M.; Krabbenhoft, David P.

    2016-02-29

    Mercury is a globally distributed pollutant that threatens human and ecosystem health. Even protected areas, such as national parks, are subjected to mercury contamination because it is delivered through atmospheric deposition, often after long-range transport. In aquatic ecosystems, certain environmental conditions can promote microbial processes that convert inorganic mercury to an organic form (methylmercury). Methylmercury biomagnifies through food webs and is a potent neurotoxicant and endocrine disruptor. The U.S. Geological Survey (USGS), the University of Maine, and the National Park Service (NPS) Air Resources Division are working in partnership at more than 50 national parks across the United States, and with citizen scientists as key participants in data collection, to develop dragonfly nymphs as biosentinels for mercury in aquatic food webs. To validate the use of these biosentinels, and gain a better understanding of the connection between biotic and abiotic pools of mercury, this project also includes collection of landscape data and surface-water chemistry including mercury, methylmercury, pH, sulfate, and dissolved organic carbon and sediment mercury concentration. Because of the wide geographic scope of the research, the project also provides a nationwide “snapshot” of mercury in primarily undeveloped watersheds.

  16. Dependence of crack growth kinetics on dendrite orientation and water chemistry for Alloy 182 weld metal in high-temperature water

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Zhanpeng, E-mail: zplu@shu.edu.cn [Institute of Materials Science, School of Materials Science and Engineering, Shanghai University, Shanghai 200072 (China); New Industry Creation Hatchery Center, Tohoku University, Sendai 980-8579 (Japan); Chen, Junjie [Institute of Materials Science, School of Materials Science and Engineering, Shanghai University, Shanghai 200072 (China); Shoji, Tetsuo [New Industry Creation Hatchery Center, Tohoku University, Sendai 980-8579 (Japan); Meng, Fanjiang [Shanghai Nuclear Engineering Research & Design Institute, Shanghai 200233 (China)

    2015-03-15

    Highlights: • SCC paths along dendrite directions in both T–S and T–L specimens of Alloy 182. • Higher SCC growth rates in T–S orientation specimen than in T–L orientation specimen. • CGR increased with increasing dissolved oxygen. • Apparently negative da/dt curve by ACPD in hydrogen saturated water. - Abstract: Stress corrosion cracking growth rates of Alloy 182 weld metals in T–S and T–L orientations in 288 °C pure water with various dissolved oxygen and hydrogen concentrations were measured. Extensive inter-dendritic stress corrosion cracking paths on the side surfaces and fracture surfaces were observed. The crack growth path in the T–S orientation specimen was perpendicular to the applied loading direction, and parallel to the loading direction in the T–L specimen. Crack growth rates of the T–S specimen were significantly higher than those of the T–L specimen under the same test conditions. The crack growth rate decreased significantly with decreasing dissolved oxygen concentration. Adding dissolved hydrogen in water caused an apparent decrease of the alternating current potential drop signal during crack growth monitoring.

  17. Structure of large nitrate-water clusters at ambient temperatures: simulations with effective fragment potentials and force fields with implications for atmospheric chemistry.

    Science.gov (United States)

    Miller, Yifat; Thomas, Jennie L; Kemp, Daniel D; Finlayson-Pitts, Barbara J; Gordon, Mark S; Tobias, Douglas J; Gerber, R Benny

    2009-11-19

    Structural properties of large NO(3)(-).(H(2)O)(n) (n = 15-500) clusters are studied by Monte Carlo simulations using effective fragment potentials (EFPs) and by classical molecular dynamics simulations using a polarizable empirical force field. The simulation results are analyzed with a focus on the description of hydrogen bonding and solvation in the clusters. In addition, a comparison between the electronic structure based EFP and the classical force field description of the 32 water cluster system is presented. The EFP simulations, which focused on the cases of n = 15 and 32, show an internal, fully solvated structure and a "surface adsorbed" structure for the 32 water cluster at 300 K, with the latter configuration being more probable. The internal solvated structure and the "surface adsorbed" structure differ considerably in their hydrogen bonding coordination numbers. The force field based simulations agree qualitatively with these results, and the local geometry of NO(3)(-) and solvation at the surface-adsorbed site in the force field simulations are similar to those predicted using EFPs. Differences and similarities between the description of hydrogen bonding of the anion in the two approaches are discussed. Extensive classical force field based simulations at 250 K predict that long time scale stability of "internal" NO(3)(-), which is characteristic of extended bulk aqueous interfaces, emerges only for n > 300. Ab initio Møller-Plesset perturbation theory is used to test the geometries of selected surface and interior anions for n = 32, and the results are compared to the EFP and MD simulations. Qualitatively, all approaches agree that surface structures are preferred over the interior structures for clusters of this size. The relatively large aqueous clusters of NO(3)(-) studied here are of comparable size to clusters that lead to new particle formation in air. Nitrate ions on the surface of such clusters may have significantly different photochemistry

  18. Effects of water chemistry on decolorization in three photochemical processes: Pro and cons of the UV/AA process.

    Science.gov (United States)

    Wu, Bingdang; Yin, Ran; Zhang, Guoyang; Yu, Chao; Zhang, Shujuan

    2016-11-15

    The poor selectivity of hydroxyl radicals is a major restriction in the practical application of the UV/H2O2 process for dyeing wastewater treatment. As an alternative, the target-selective UV/acetylacetone (AA) process was found highly efficient for dye decolorization. For the proper selection and application of the two photochemical processes, the effects of water matrices, including common inorganic anions (Cl(-), SO4(2-), NO3(-), HCO3(-)), natural organic matter, metal cations (Mg(2+), Mn(2+), Cu(2+), Fe(3+), Cr(3+)), and temperature, on the photo-degradation of an azo dye, Acid Orange 7 (AO7), were systematically investigated. The experimental results demonstrate that the UV/AA process was more sensitive to inner filter effect. NO3(-), Cu(2+), and Fe(3+) were all detrimental to the UV/AA process, whereas at certain concentrations they were beneficial to the UV/H2O2 process. However, even with severe inhibitory effects, the decolorization efficiency of the UV/AA process was still several times higher than that of the UV/H2O2 process. The results are helpful for us to better understand the mechanisms behind the UV/AA process and may shed light on the application of UV-based advanced oxidation processes for wastewater treatment.

  19. The Romanian perspective on geothermal energy resources. The chemistry of the geothermal waters from Oradea Triassic aquifer

    Directory of Open Access Journals (Sweden)

    Ruxandra M. Petrescu-Mag

    2009-01-01

    Full Text Available In 2008, the European Commission put forward a proposal for a new directive (COM (200830 on renewable energies to replace the existing measures adopted in 2001. According to the proposal, each member state should increase its share of renewable energies - such as solar, wind or hydro - in an effort to boost the EU's share from 8.5% today to 20% by 2020. According to Cohuţ & Bendea (2000 in Romania are over 200 wells drilled to depths between 800 and 3500 m that encountered geothermalresources at temperatures from 40 to 120 °C. These wells have a total thermal capacity of about 480 Mwt. The Oradea aquifer was identified between 1963-1964 by the drills 4005 and 4006. To establish the content of the major elements of the geothermal waters from the production wells from Oradea, the geothermal fluids were sampled and analyzed during six months (since October 2007 to March 2008, by using ion chromatographic (IC method. In this period of the year, the geothermal installations are used at the maximum capacity.

  20. Long-term changes in precipitation and stream water chemistry in small forest and moorland catchments at Beddgelert Forest, north Wales

    Directory of Open Access Journals (Sweden)

    B. Reynolds

    2004-01-01

    Full Text Available Changes in the chemistry of bulk precipitation and stream water between 1982 and 2000 are described for small moorland and forest catchments located within Beddgelert Forest in north Wales. Two forest catchments were partially clearfelled in 1984 (D2; 68% and D4; 28% whilst a third (D3 remained as an unfelled control until autumn / winter 1998/99 when partial felling took place in the headwaters. Over the monitoring period, the annual mean pH of bulk precipitation increased from 4.6 to 5.1 whilst the annual mean non-seasalt sulphate concentration decreased from 0.53 mg S l-1 in 1985 to 0.24 mg S l-1 in 2000. Since 1985, the annual wet deposition flux of non-seasalt sulphur decreased by 50% to 8.4 kg S ha-1 yr–1 in 2000. Annual mean inorganic nitrogen concentrations and annual wet deposition fluxes have remained relatively unchanged since 1982. The decrease in atmospheric sulphur deposition is reflected by decreased annual mean concentrations of non-seasalt sulphur, acidity, aluminium and calcium in all four streams irrespective of clearfelling activities. Annual variations in nitrate-N and potassium concentrations in the forest streams, largely determined by pulses of leaching following forest clearance, had no effect on stream acidity. In common with UK upland catchments, annual mean concentrations of dissolved organic carbon have increased from about 1 mg C l-1 in 1985 to between 1.5 and 2 mg C l-1 in 2000, although there is considerable year to year variability. Two boreholes drilled adjacent to catchments D3 and D4 have confirmed the presence of alkaline, base rich groundwater at Beddgelert. Although the boreholes are only 150 m apart, there are large differences in chemistry suggesting that different groundwater reservoirs have been intercepted providing further evidence of the complexity and heterogeneity of groundwater systems in upland catchments. Keywords: acid deposition, acidification, recovery, forestry, clearfelling, trends

  1. Hydrogeology, water chemistry, and transport processes in the zone of contribution of a public-supply well in Albuquerque, New Mexico, 2007-9

    Science.gov (United States)

    Bexfield, Laura M.; Jurgens, Bryant C.; Crilley, Dianna M.; Christenson, Scott C.

    2012-01-01

    The National Water-Quality Assessment Program (NAWQA) of the U.S. Geological Survey began a series of groundwater studies in 2001 in representative aquifers across the Nation in order to increase understanding of the factors that affect transport of anthropogenic and natural contaminants (TANC) to public-supply wells. One of 10 regional-scale TANC studies was conducted in the Middle Rio Grande Basin (MRGB) in New Mexico, where a more detailed local-scale study subsequently investigated the hydrogeology, water chemistry, and factors affecting the transport of contaminants in the zone of contribution of one 363-meter (m) deep public-supply well in Albuquerque. During 2007 through 2009, samples were collected for the local-scale study from 22 monitoring wells and 3 public-supply (supply) wells for analysis of major and trace elements, arsenic speciation, nutrients, dissolved organic carbon, volatile organic compounds (VOCs), dissolved gases, stable isotopes, and tracers of young and old water. To study groundwater chemistry and ages at various depths within the aquifer, the monitoring wells were divided into three categories: (1) each shallow well was screened across the water table or had a screen midpoint within 18.3 m of the water level in the well; (2) each intermediate well had a screen midpoint between about 27.1 and 79.6 m below the water level in the well; and (3) each deep well had a screen midpoint about 185 m or more below the water level in the well. The 24-square-kilometer study area surrounding the "studied supply well" (SSW), one of the three supply wells, consists of primarily urban land within the MRGB, a deep alluvial basin with an aquifer composed of unconsolidated to moderately consolidated deposits of sand, gravel, silt, and clay. Conditions generally are unconfined, but are semiconfined at depth. Groundwater withdrawals for public supply have substantially changed the primary direction of flow from northeast to southwest under predevelopment

  2. Computational chemistry

    Science.gov (United States)

    Arnold, J. O.

    1987-01-01

    With the advent of supercomputers, modern computational chemistry algorithms and codes, a powerful tool was created to help fill NASA's continuing need for information on the properties of matter in hostile or unusual environments. Computational resources provided under the National Aerodynamics Simulator (NAS) program were a cornerstone for recent advancements in this field. Properties of gases, materials, and their interactions can be determined from solutions of the governing equations. In the case of gases, for example, radiative transition probabilites per particle, bond-dissociation energies, and rates of simple chemical reactions can be determined computationally as reliably as from experiment. The data are proving to be quite valuable in providing inputs to real-gas flow simulation codes used to compute aerothermodynamic loads on NASA's aeroassist orbital transfer vehicles and a host of problems related to the National Aerospace Plane Program. Although more approximate, similar solutions can be obtained for ensembles of atoms simulating small particles of materials with and without the presence of gases. Computational chemistry has application in studying catalysis, properties of polymers, all of interest to various NASA missions, including those previously mentioned. In addition to discussing these applications of computational chemistry within NASA, the governing equations and the need for supercomputers for their solution is outlined.

  3. Free Radical Chemistry of Disinfection Byproducts 1: Kinetics of Hydrated Electron and Hydroxyl Radical Reactions with Halonitromethanes in Water

    Energy Technology Data Exchange (ETDEWEB)

    B. J. Mincher; R. V. Fox; S. P. Mezyk; T. Helgeson; S. K. Cole; W. J. Cooper; P. R. Gardinali

    2006-01-01

    Halonitromethanes are disinfection-byproducts formed during ozonation and chlorine/chloramine treatment of waters that contain bromide ion and natural organic matter. In this study, the chemical kinetics of the free-radical-induced degradations of a series of halonitromethanes were determined. Absolute rate constants for hydroxyl radical, OH, and hydrated electron, eaq-, reaction with both chlorinated and brominated halonitromethanes were measured using the techniques of electron pulse radiolysis and transient absorption spectroscopy. The bimolecular rate constants obtained, k (M-1 s-1), for eaq-/OH, respectively, were the following: chloronitromethane (3.01 ± 0.40) × 1010/(1.94 ± 0.32) × 108; dichloronitromethane (3.21 ± 0.17) × 1010/(5.12 ± 0.77) × 108; bromonitromethane (3.13 ± 0.06) × 1010/(8.36 ± 0.57) × 107; dibromonitromethane (3.07 ± 0.40) × 1010/(4.75 ± 0.98) × 108; tribromonitromethane (2.29 ± 0.39) × 1010/(3.25 ± 0.67) × 108; bromochloronitromethane (2.93 ± 0.47) × 1010/(4.2 ± 1.1) × 108; bromodichloronitromethane (2.68 ± 0.13) × 1010/(1.02 ± 0.15) × 108; and dibromochloronitromethane (2.95 ± 0.43) × 1010 / (1.80 ± 0.31) × 108 at room temperature and pH ~7. Comparison data were also obtained for hydroxyl radical reaction with bromoform (1.50 ± 0.05) × 108, bromodichloromethane (7.11 ± 0.26) × 107, and chlorodibromomethane (8.31 ± 0.25) × 107 M-1 s-1, respectively. These rate constants are compared to recently obtained data for trichloronitromethane and bromonitromethane, as well as to other established literature data for analogous compounds.

  4. Interpretation of trends in acidic deposition and surface water chemistry in Scotland during the past three decades

    Directory of Open Access Journals (Sweden)

    R. Harriman

    2001-01-01

    . Interpretation of chemical and biological trends was clearly influenced by the choice of the time series, especially in relation to deposition and climatic changes. Nevertheless, all the fresh waters included in this study are currently in the best ecological condition since the 1970s in the context of recovery from acidification. Keywords: deposition, trends, acidification, forestry, recovery, fish, climate

  5. Theoretical chemistry periodicities in chemistry and biology

    CERN Document Server

    Eyring, Henry

    1978-01-01

    Theoretical Chemistry: Periodicities in Chemistry and Biology, Volume 4 covers the aspects of theoretical chemistry. The book discusses the stably rotating patterns of reaction and diffusion; the chemistry of inorganic systems exhibiting nonmonotonic behavior; and population cycles. The text also describes the mathematical modeling of excitable media in neurobiology and chemistry; oscillating enzyme reactions; and oscillatory properties and excitability of the heart cell membrane. Selected topics from the theory of physico-chemical instabilities are also encompassed. Chemists, mechanical engin

  6. Antiscaling efficacy of CaCO3 and CaSO4 on polyethylene glycol (PEG)-modified reverse osmosis membranes in the presence of humic acid: interplay of membrane surface properties and water chemistry.

    Science.gov (United States)

    Ray, Jessica R; Wong, Whitney; Jun, Young-Shin

    2017-02-15

    Mineral scaling persists in many water treatment processes. More specifically, it can significantly reduce the efficacy of aromatic polyamide (PA) membranes during reverse osmosis (RO) water treatment. Previous studies have integrated hydrophilic materials, such as polyethylene glycol (PEG), onto RO membranes to combat scaling from generally hydrophobic feed water constituents; however, there are still outstanding knowledge gaps regarding the interplay of the modified membrane surface chemistry and the water chemistry in complex RO feed waters. In this work, we have investigated the mechanisms of hydrophilic PEG-grafted PA membranes in reducing mineral scaling from calcium carbonate (CaCO3) and calcium sulfate (CaSO4) in the presence of humic acid (HA). Based on surface and solution analyses, we found that colloidal formation was significantly reduced on PA-PEG surfaces in systems without HA. When HA was introduced, CaCO3 scaling was reduced on both virgin and PA-PEG membrane surfaces; while, interestingly, synergistic PEG-HA-CaSO4 interactions increased CaSO4 colloidal formation on PA-PEG membranes. Promoted CaSO4 formation results from a high negative surface charge near the PEG-modified membrane surface when HA and SO4(2-) are present, attracting more Ca(2+) to form CaSO4. The results of this work provide new information about colloidal formation at water-membrane interfaces for designing better PEG and PEG-based scale-resistant desalination membranes.

  7. Surface chemistry

    CERN Document Server

    Desai, KR

    2008-01-01

    The surface Chemistry of a material as a whole is crucially dependent upon the Nature and type of surfaces exposed on crystallites. It is therefore vitally important to independently Study different, well - defined surfaces through surface analytical techniques. In addition to composition and structure of surface, the subject also provides information on dynamic light scattering, micro emulsions, colloid Stability control and nanostructures. The present book endeavour to bring before the reader that the understanding and exploitation of Solid state phenomena depended largely on the ability to

  8. Organometallic chemistry in non-classical environments.

    Science.gov (United States)

    Dyson, Paul J

    2011-01-01

    A summary of our on-going research on organometallic chemistry is provided with an emphasis on the function, reactivity and mechanisms of organometallic compounds in water, ionic liquids and in living systems. The role of organometallic compounds in both catalysis and medicinal chemistry are briefly described.

  9. Chemical experiment - the basis in learning chemistry

    Directory of Open Access Journals (Sweden)

    N. Dalabayeva

    2012-12-01

    Full Text Available Particular classification and method carrying out chemical experiment and their place in learning chemistry was considered. And also was showed that an application of kinds of chemical experiments competence develops in learning at the decision of experimental problems in chemistry. Features of solubility of firm substances in water are discussed at the chemical experiment and the process of dissolution.

  10. Chemical experiment - the basis in learning chemistry

    OpenAIRE

    N. Dalabayeva

    2012-01-01

    Particular classification and method carrying out chemical experiment and their place in learning chemistry was considered. And also was showed that an application of kinds of chemical experiments competence develops in learning at the decision of experimental problems in chemistry. Features of solubility of firm substances in water are discussed at the chemical experiment and the process of dissolution.

  11. An introduction to serious nuclear accident chemistry

    OpenAIRE

    Mark Russell St. John Foreman

    2015-01-01

    A review of the chemistry occurring inside a nuclear power plant during a serious reactor accident is presented. This includes some aspects of the behavior of nuclear fuel, its cladding, cesium and iodine. This review concentrates on the chemistry of an accident in a water-cooled reactor loaded with uranium dioxide or mixed metal oxide fuel.

  12. The discovery by Gh. Benga of the first water channel protein in 1985 in Cluj-Napoca, Romania, A few years before P. Agre (2003 Nobel Prize in Chemistry).

    Science.gov (United States)

    Cucuianu, M

    2006-01-01

    The first water channel protein, now called aquaporin 1, was identified or "seen" in situ in the human red blood cell membrane by Benga's group in 1985. It was again "seen" when it was by chance purified by Agre'group in 1988 and was again identified when its main feature, the water transport property, was found by Agre's group in 1992. Consequently, the omission of Gh. Benga from the 2003 Nobel Prize in Chemistry (half of which was awarded to P. Agre "for the discovery of the water channels") is a new mistake in the award of Nobel Prizes. The growing recognition of the priority of Gh. Benga over P. Agre in the discovery of water channels is documented in this paper.

  13. Science Update: Inorganic Chemistry

    Science.gov (United States)

    Rawls, Rebecca

    1978-01-01

    This first in a series of articles describing the state of the art of various branches of chemistry reviews inorganic chemistry, including bioinorganic, photochemistry, organometallic, and solid state chemistries. (SL)

  14. Phoenix's Wet Chemistry Lab

    Science.gov (United States)

    2008-01-01

    This is an illustration of soil analysis on NASA's Phoenix Mars Lander's Wet Chemistry Lab (WCL) on board the Microscopy, Electrochemistry, and Conductivity Analyzer (MECA) instrument. By dissolving small amounts of soil in water, WCL will attempt to determine the pH, the abundance of minerals such as magnesium and sodium cations or chloride, bromide and sulfate anions, as well as the conductivity and redox potential. The Phoenix Mission is led by the University of Arizona, Tucson, on behalf of NASA. Project management of the mission is by NASA's Jet Propulsion Laboratory, Pasadena, Calif. Spacecraft development is by Lockheed Martin Space Systems, Denver.

  15. Phoenix's Wet Chemistry Lab

    Science.gov (United States)

    2008-01-01

    This is an illustration of the analytical procedure of NASA's Phoenix Mars Lander's Wet Chemistry Lab (WCL) on board the Microscopy, Electrochemistry, and Conductivity Analyzer (MECA) instrument. By dissolving small amounts of soil in water, WCL can determine the pH, the abundance of minerals such as magnesium and sodium cations or chloride, bromide and sulfate anions, as well as the conductivity and redox potential. The Phoenix Mission is led by the University of Arizona, Tucson, on behalf of NASA. Project management of the mission is by NASA's Jet Propulsion Laboratory, Pasadena, Calif. Spacecraft development is by Lockheed Martin Space Systems, Denver.

  16. Astronomical chemistry.

    Science.gov (United States)

    Klemperer, William

    2011-01-01

    The discovery of polar polyatomic molecules in higher-density regions of the interstellar medium by means of their rotational emission detected by radioastronomy has changed our conception of the universe from essentially atomic to highly molecular. We discuss models for molecule formation, emphasizing the general lack of thermodynamic equilibrium. Detailed chemical kinetics is needed to understand molecule formation as well as destruction. Ion molecule reactions appear to be an important class for the generally low temperatures of the interstellar medium. The need for the intrinsically high-quality factor of rotational transitions to definitively pin down molecular emitters has been well established by radioastronomy. The observation of abundant molecular ions both positive and, as recently observed, negative provides benchmarks for chemical kinetic schemes. Of considerable importance in guiding our understanding of astronomical chemistry is the fact that the larger molecules (with more than five atoms) are all organic.

  17. Combustion chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Brown, N.J. [Lawrence Berkeley Laboratory, CA (United States)

    1993-12-01

    This research is concerned with the development and use of sensitivity analysis tools to probe the response of dependent variables to model input variables. Sensitivity analysis is important at all levels of combustion modeling. This group`s research continues to be focused on elucidating the interrelationship between features in the underlying potential energy surface (obtained from ab initio quantum chemistry calculations) and their responses in the quantum dynamics, e.g., reactive transition probabilities, cross sections, and thermal rate coefficients. The goals of this research are: (i) to provide feedback information to quantum chemists in their potential surface refinement efforts, and (ii) to gain a better understanding of how various regions in the potential influence the dynamics. These investigations are carried out with the methodology of quantum functional sensitivity analysis (QFSA).

  18. Advanced Chemistry Laboratory

    Data.gov (United States)

    Federal Laboratory Consortium — Description/History: Chemistry laboratory The Advanced Chemistry Laboratory (ACL) is a unique facility designed for working with the most super toxic compounds known...

  19. Science Update: Inorganic Chemistry.

    Science.gov (United States)

    Rawls, Rebecca

    1981-01-01

    Describes areas of inorganic chemistry which have changed dramatically in the past year or two, including photochemistry, electrochemistry, organometallic complexes, inorganic reaction theory, and solid state chemistry. (DS)

  20. Plasma chemistry and organic synthesis

    Science.gov (United States)

    Tezuka, M.

    1980-01-01

    The characteristic features of chemical reactions using low temperature plasmas are described and differentiated from those seen in other reaction systems. A number of examples of applications of plasma chemistry to synthetic reactions are mentioned. The production of amino acids by discharge reactions in hydrocarbon-ammonia-water systems is discussed, and its implications for the origins of life are mentioned.

  1. B-Li水化学对核电金属材料腐蚀的影响%Effect of B-Li Water Chemistry on Corrosion of Metal Materials of Nuclear Power Plant

    Institute of Scientific and Technical Information of China (English)

    宋利君; 刘飞华; 李成涛; 李岩; 鲁俊东

    2014-01-01

    This paper represented the development trend of primary B-Li water chemistry conditions in pressurized water reactor nuclear power plant,and the functions of water chemistry in the corrosion products and dose rate.The effect of B concentration,Li concentration and pH on the PWSCC sensitivity,the crack propagation rate and the corrosion product release rate of nickel-based alloys,stainless steel,and zirconium alloy had been reviewed.The advantage of enriched boric acid application in nuclear power plant was also analyzed.The higher pH value of primary water chemistry have the benefit of reducing corrosion of metal materials in nuclear power plant,and improve the safety and reliability of nuclear power plants.%本文阐述了压水堆核电站一回路B-Li水化学工况控制的发展趋势,及其对腐蚀产物、降低剂量率的作用;概括了B浓度、Li浓度及 pH 值对镍基合金、不锈钢、锆合金的 PWSCC敏感性、裂纹扩展速率、腐蚀产物释放速率等性能的影响;分析了核电站应用富集硼酸的积极作用。一回路水化学控制在较高pH 有利于减少核电站金属材料的腐蚀,提高核电站的安全与可靠性。

  2. The dissolution rate of unirratiated uranium dioxide under repository conditions: The influence of fuel and water chemistry, dissolved oxygen, and temperature

    Science.gov (United States)

    Casella, Amanda J.

    The dissolution rate of both unirradiated UO2 and spent fuel has been studied by numerous countries as part of the performance assessments of proposed geologic repositories. The effects of variables such as temperature, dissolved oxygen, and water and fuel chemistry on the dissolution rates of the fuel are necessary to provide a quantitative estimate of the potential dose over geologic time frames. The primary objective of this research was to determine the influence these parameters have on the dissolution rate of unirradiated UO2 under Yucca Mountain repository conditions and compare them to the current Yucca Mountain Model. Fuels containing between 0 and 8 wt% Gd2O3-doped UO2 were tested in a single-pass flow-through setup. These tests have verified that in bicarbonate solutions as temperature increased the dissolution rate increased. However, the presence of silicate in the feedwater altered the system and lowered the dissolution rate at higher temperatures. Pure UO 2 samples exhibited a dependence on the dissolved oxygen concentration, which in the current experiments was varied from 3.0 to 8.7 ppm. The significance of this dissolved oxygen dependence increased with rising temperature. At 75ºC the powder samples had a maximum dependence of 0.7, although the fragment samples had a much larger dependence up to 2.2. For the case of the Gd2O3-doped samples, there was minimal oxygen dependence at any temperature. The Gd2O3-dopant stabilized the fuel matrix, which lowered the dissolution rates by over an order of magnitude at the higher dopant levels. This effect in lowering the dissolution rate was more pronounced at higher temperatures, and additional dopant continued to decrease the dissolution rate up to the 4 wt% Gd2O3-doped UO2 tested. The dissolution rates for pure UO2 compared reasonably well with the Yucca Mountain Model for tests performed at 50ºC and 75ºC, but were found to be approximately half the values predicted by the model at 25ºC. After long

  3. Origin and evolution of oilfield brines from Tertiary strata in western Qaidam Basin: Constraints from 87Sr/86Sr, δD, δ18O, δ34S and water chemistry

    Institute of Scientific and Technical Information of China (English)

    FAN Qishun; MA Haizhou; LAI Zhongping; TAN Hongbing; LI Tingwei

    2010-01-01

    Chemistry of major and minor elements, 87Sr/86Sr, δD, δ18O and δ34S of brines were measured from Tertiary strata and Quaternary salt lakes in the western Qaidam Basin. The water chemistry data show that all oilfield brines are CaCl2 type. They were enriched in Ca2+, B3+, Li+, Sr2+, Br-, and were depleted in Mg2+, SO42-, which indicated that these brines had the characteristics of deeply circulated water. The relationship between δD and δ18O shows that all data of these brines decline towards the Global Meteoric Water Line (GWL) and Qaidam Meteoric Water Line (QWL), and that the intersection between oilfield brines and Meteoric Water Lines was close to the local spring and fresh water in the piedmont in the western Qaidam Basin. The results suggest that oilfield brines has initially originated from meteoric water, and then might be affected by water-rock metamorphose, because most oilfield brines distribute in the range of metamorphosing water. The 87Sr/86Sr values of most oilfield brines range from 0.71121 to 0.71194, and was less than that in salt lake water (>0.712), but close to that of halite in the study area. These imply that salt dissolution occurred in the process of migration. In addition, all oilfield brines have obviously much positive δ34S values (ranging from 26.46‰ to 54.57‰) than that of salt lake brines, which was caused by bacterial sulfate reduction resulting in positive shift of δ34S value and depleteed SO42- in oilfield brines. Combined with water chemical data and δD, δ18O, 87Sr/86Sr, δ34S values, we concluded that oilfield brines mainly originate from the deeply circulated meteoric waters, and then are affected by salt dissolution, water-rock metamorphose, sulfate reduction and dolomitization during the process of migration. These processes alter the chemical compositions of oilfield brines and accumulate rich elements (such as B, Li, Sr, Br, K and so on) for sustainable utilization of salt lake resources in the Qaidam Basin.

  4. The Origin of Carbon-bearing Volatiles in Surprise Valley Hot Springs in the Great Basin: Carbon Isotope and Water Chemistry Characterizations

    Science.gov (United States)

    Fu, Qi; Socki, Richard A.; Niles, Paul B.; Romanek, Christopher; Datta, Saugata; Darnell, Mike; Bissada, Adry K.

    2013-01-01

    There are numerous hydrothermal fields within the Great Basin of North America, some of which have been exploited for geothermal resources. With methane and other carbon-bearing compounds being observed, in some cases with high concentrations, however, their origins and formation conditions remain unknown. Thus, studying hydrothermal springs in this area provides us an opportunity to expand our knowledge of subsurface (bio)chemical processes that generate organic compounds in hydrothermal systems, and aid in future development and exploration of potential energy resources as well. While isotope measurement has long been used for recognition of their origins, there are several secondary processes that may generate variations in isotopic compositions: oxidation, re-equilibration of methane and other alkanes with CO2, mixing with compounds of other sources, etc. Therefore, in addition to isotopic analysis, other evidence, including water chemistry and rock compositions, are necessary to identify volatile compounds of different sources. Surprise Valley Hot Springs (SVHS, 41 deg 32'N, 120 deg 5'W), located in a typical basin and range province valley in northeastern California, is a terrestrial hydrothermal spring system of the Great Basin. Previous geophysical studies indicated the presence of clay-rich volcanic and sedimentary rocks of Tertiary age beneath the lava flows in late Tertiary and Quaternary. Water and gas samples were collected for a variety of chemical and isotope composition analyses, including in-situ pH, alkalinity, conductivity, oxidation reduction potential (ORP), major and trace elements, and C and H isotope measurements. Fluids issuing from SVHS can be classified as Na-(Cl)-SO4 type, with the major cation and anion being Na+ and SO4(2-), respectively. Thermodynamic calculation using ORP and major element data indicated that sulfate is the most dominant sulfur species, which is consistent with anion analysis results. Aquifer temperatures at depth

  5. The Origin of Carbon-bearing Volatiles in Surprise Valley Hot Springs in the Great Basin: Carbon Isotope aud Water Chemistry Characterizations

    Science.gov (United States)

    Fu, Qi; Socki, Richard A.; Niles, Paul B.; Romanek, Christopher; Datta, Saugata; Darnell, Mike; Bissada, Adry K.

    2013-01-01

    There are numerous hydrothermal fields within the Great Basin of North America, some of which have been exploited for geothermal resources. With methane and other carbon-bearing compounds being observed, in some cases with high concentrations, however, their origins and formation conditions remain unknown. Thus, studying hydrothermal springs in this area provides us an opportunity to expand our knowledge of subsurface (bio)chemical processes that generate organic compounds in hydrothermal systems, and aid in future development and exploration of potential energy resources as well. While isotope measurement has long been used for recognition of their origins, there are several secondary processes that may generate variations in isotopic compositions: oxidation, re-equilibration of methane and other alkanes with CO2, mixing with compounds of other sources, etc. Therefore, in addition to isotopic analysis, other evidence, including water chemistry and rock compositions, are necessary to identify volatile compounds of different sources. Surprise Valley Hot Springs (SVHS, 41º32'N, 120º5'W), located in a typical basin and range province valley in northeastern California, is a terrestrial hydrothermal spring system of the Great Basin. Previous geophysical studies indicated the presence of clay-rich volcanic and sedimentary rocks of Tertiary age beneath the lava flows in late Tertiary and Quaternary. Water and gas samples were collected for a variety of chemical and isotope composition analyses, including in-situ pH, alkalinity, conductivity, oxidation reduction potential (ORP), major and trace elements, and C and H isotope measurements. Fluids issuing from SVHS can be classified as Na-(Cl)-SO4 type, with the major cation and anion being Na+ and SO4 2-, respectively. Thermodynamic calculation using ORP and major element data indicated that sulfate is the most dominant sulfur species, which is consistent with anion analysis results. Aquifer temperatures at depth estimated

  6. The Origin of Carbon-bearing Volatiles in Surprise Valley Hot Springs in the Great Basin: Carbon Isotope and Water Chemistry Characterizations

    Science.gov (United States)

    Fu, Q.; Socki, R.; Niles, P. B.; Romanek, C. S.; Datta, S.; Darnell, M.; Bissada, A. K.

    2013-12-01

    There are numerous hydrothermal fields within the Great Basin of North America, some of which have been exploited for geothermal resources. With methane and other carbon-bearing compounds being observed, however, their origins and formation conditions remain unknown. Thus, studying hydrothermal springs in this area provides us an opportunity to understand subsurface (bio)chemical processes that generate organic compounds, and aid in future development and exploration of potential energy resources as well. While isotope measurement has long been used for identification of their origins, there are secondary processes that may generate variations in isotopic compositions: oxidation, re-equilibration of methane and other alkanes with CO2, mixing with compounds of other sources, etc. Therefore, in addition to isotopic analysis, other lines of evidence, including water chemistry and rock compositions, are necessary to identify origins of volatile compounds. Surprise Valley Hot Springs (SVHS, 41°32'N, 120°5'W), located in a typical basin and range province in northeastern California, is a terrestrial hydrothermal spring system of the Great Basin. Previous geophysical studies indicated the presence of clay-rich volcanic and sedimentary rocks of Tertiary age beneath the lava flows during late Tertiary and Quaternary. Water and gas samples were collected for a variety of chemical and isotope composition analyses, including in-situ pH, alkalinity, oxidation reduction potential (ORP), major and trace elements, and C and H isotope measurements. Fluids issuing from SVHS can be classified as Na-(Cl)-SO4 type, with the major cation and anion being Na+ and SO42-, respectively. Thermodynamic calculation using ORP and major element data indicated that sulfate is the most dominant sulfur species, which is consistent with anion analysis results. Aquifer temperatures at depth estimated by both dissolved SiO2 and Na-K-Ca geothermometers are in the range of 125.0 to 135.4 °C, and

  7. Using Mole Ratios of Electrolytic Products of Water for Analysis of Household Vinegar: An Experiment for the Undergraduate Physical Chemistry Laboratory

    Science.gov (United States)

    Dabke, Rajeev B.; Gebeyehu, Zewdu

    2012-01-01

    A simple 3-h physical chemistry undergraduate experiment for the quantitative analysis of acetic acid in household vinegar is presented. The laboratory experiment combines titration concept with electrolysis and an application of the gas laws. A vinegar sample was placed in the cathode compartment of the electrolysis cell. Electrolysis of water…

  8. Water

    Science.gov (United States)

    ... www.girlshealth.gov/ Home Nutrition Nutrition basics Water Water Did you know that water makes up more ... to drink more water Other drinks How much water do you need? top Water is very important, ...

  9. 2nd European Meeting on Environmental Chemistry

    OpenAIRE

    Lichtfouse, Eric; Elbisser, Brigitte

    2001-01-01

    International audience; ORAL SESSIONS: AIR POLLUTION - ORGANIC POLLUTANTS, WATER AND FOOD POLLUTION - ORGANIC POLLUTANTS, SOIL POLLUTION - TOXIC METALS, ANALYTICAL METHODS FOR ENVIRONMENTAL SCIENCE, GREEN CHEMISTRY, ECOTOXICOLOGY, STABLE ISOTOPES FOR ENVIRONMENTAL SCIENCE, WATER POLLUTION - TOXIC METALS, ANALYTICAL METHODS FOR ENVIRONMENTAL SCIENCE, SOIL POLLUTION - ORGANIC POLLUTANTSPOSTER SESSIONS: AIR POLLUTION - TOXIC METALS, AIR POLLUTION - ORGANIC POLLUTANTS, WATER POLLUTION - TOXIC MET...

  10. Nitrogen Compounds in Radiation Chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Sims, H.E. [NNL Sellafield (United Kingdom); Dey, G.R. [Radiation and Photochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Vaudey, C.E.; Peaucelle, C. [Institut de Physique Nucleaire de Lyon - IPNL, 69 - Lyon (France); Boucher, J.L. [Lab. de Chimie et Biochimie Pharmacologiques et Toxicologiques, UMR 8601 CNRS 45 rue des Saints Peres, 75270 Paris cedex 06, Univ Paris 5, 75 (France); Toulhoat, N. [Institut de Physique Nucleaire de Lyon (France); Commissariat a l' Energie Atomique CEA/DEN, Centre de Saclay (France); Bererd, N. [Institut de Physique Nucleaire de Lyon (France); IUT Departement Chimie, Universite Claude Bernard Lyon 1 (France); Koppenol, W.H. [Department of Chemistry and Applied Biosciences, ETH Zurich (Switzerland); Janata, E. [Helmholtz-Zentrum fuer Materialien und Energie, Solar Energy Research, Berlin (Germany); Dauvois, V.; Durand, D.; Legand, S.; Roujou, J.L.; Doizi, D.; Dannoux, A.; Lamouroux, C. [Laboratoire de Speciation des Radionucleides et des Molecules, DEN/DPC/Service d' Etude du Comportement des Radionucleides, CEA Saclay, 91 - Gif sur yvette (France)

    2009-07-01

    Water radiolysis in presence of N{sub 2} is probably the topic the most controversy in the field of water radiolysis. It still exists a strong discrepancy between the different reports of ammonia formation by water radiolysis in presence of N{sub 2} and moreover in absence of oxygen there is no agreement on the formation or not of nitrogen oxide like NO{sub 2}- and NO{sub 3}-. These discrepancies come from multiple sources: - the complexity of the reaction mechanisms where nitrogen is involved - the experimental difficulties - and, the irradiation conditions. The aim of the workshop is to capitalize the knowledge needed to go further in simulations and understanding the problems caused (or not) by the presence of nitrogen / water in the environment of radioactive materials. Implications are evident in terms of corrosion, understanding of biological systems and atmospheric chemistry under radiation. Topics covered include experimental and theoretical approaches, application and fundamental researches: - Nitrate and Ammonia in radiation chemistry in nuclear cycle; - NOx in biological systems and atmospheric chemistry; - Formation of Nitrogen compounds in Nuclear installations; - Nitrogen in future power plant projects (Gen4, ITER...) and large particle accelerators. This document gathers the transparencies available for 7 of the presentations given at this workshop. These are: - H.E SIMS: 'Radiation Chemistry of Nitrogen Compounds in Nuclear Power Plant'; - G.R. DEY: 'Nitrogen Compounds Formation in the Radiolysis of Aqueous Solutions'; - C.E. VAUDEY et al.: 'Radiolytic corrosion of nuclear graphite studied with the dedicated gas irradiation cell of IPNL'; - J.L. BOUCHER: 'Roles and biosynthesis of NO in eukaryotes and prokaryotes'; - W.H. KOPPENOL: 'Chemistry of NOx'; - E. JANATA: 'Yield of OH in N{sub 2}O saturated aqueous solution'; - V. DAUVOIS: 'Analytical strategy for the study of radiolysis gases'

  11. The Chemistry of Planet Formation

    Science.gov (United States)

    Oberg, Karin I.

    2017-01-01

    Exo-planets are common, and they span a large range of compositions. The origins of the observed diversity of planetary compositions is largely unconstrained, but must be linked to the planet formation physics and chemistry. Among planets that are Earth-like, a second question is how often such planets form hospitable to life. A fraction of exo-planets are observed to be ‘physically habitable’, i.e. of the right temperature and bulk composition to sustain a water-based prebiotic chemistry, but this does not automatically imply that they are rich in the building blocks of life, in organic molecules of different sizes and kinds, i.e. that they are chemically habitable. In this talk I will argue that characterizing the chemistry of protoplanetary disks, the formation sites of planets, is key to address both the origins of planetary bulk compositions and the likelihood of finding organic matter on planets. The most direct path to constrain the chemistry in disks is to directly observe it. In the age of ALMA it is for the first time possible to image the chemistry of planet formation, to determine locations of disk snowlines, and to map the distributions of different organic molecules. Recent ALMA highlights include constraints on CO snowline locations, the discovery of spectacular chemical ring systems, and first detections of more complex organic molecules. Observations can only provide chemical snapshots, however, and even ALMA is blind to the majority of the chemistry that shapes planet formation. To interpret observations and address the full chemical complexity in disks requires models, both toy models and astrochemical simulations. These models in turn must be informed by laboratory experiments, some of which will be shown in this talk. It is thus only when we combine observational, theoretical and experimental constraints that we can hope to characterize the chemistry of disks, and further, the chemical compositions of nascent planets.

  12. IN-PACKAGE CHEMISTRY ABSTRACTION

    Energy Technology Data Exchange (ETDEWEB)

    E. Thomas

    2005-07-14

    This report was developed in accordance with the requirements in ''Technical Work Plan for Postclosure Waste Form Modeling'' (BSC 2005 [DIRS 173246]). The purpose of the in-package chemistry model is to predict the bulk chemistry inside of a breached waste package and to provide simplified expressions of that chemistry as a function of time after breach to Total Systems Performance Assessment for the License Application (TSPA-LA). The scope of this report is to describe the development and validation of the in-package chemistry model. The in-package model is a combination of two models, a batch reactor model, which uses the EQ3/6 geochemistry-modeling tool, and a surface complexation model, which is applied to the results of the batch reactor model. The batch reactor model considers chemical interactions of water with the waste package materials, and the waste form for commercial spent nuclear fuel (CSNF) waste packages and codisposed (CDSP) waste packages containing high-level waste glass (HLWG) and DOE spent fuel. The surface complexation model includes the impact of fluid-surface interactions (i.e., surface complexation) on the resulting fluid composition. The model examines two types of water influx: (1) the condensation of water vapor diffusing into the waste package, and (2) seepage water entering the waste package as a liquid from the drift. (1) Vapor-Influx Case: The condensation of vapor onto the waste package internals is simulated as pure H{sub 2}O and enters at a rate determined by the water vapor pressure for representative temperature and relative humidity conditions. (2) Liquid-Influx Case: The water entering a waste package from the drift is simulated as typical groundwater and enters at a rate determined by the amount of seepage available to flow through openings in a breached waste package.

  13. Green chemistry: A tool in Pharmaceutical Chemistry

    OpenAIRE

    Smita Talaviya; Falguni Majumdar

    2012-01-01

    Green chemistry expresses an area of research developing from scientific discoveries about pollution awareness and it utilizes a set of principles that reduces or eliminates the use or generation of hazardous substances in all steps of particular synthesis or process. Chemists and medicinal scientists can greatly reduce the risk to human health and the environment by following all the valuable principles of green chemistry. The most simple and direct way to apply green chemistry in pharmaceut...

  14. From Matter to Life:Chemistry?Chemistry!

    Institute of Scientific and Technical Information of China (English)

    Jean-Marie; LEHN

    2007-01-01

    1 Results Animate as well as inanimate matter,living organisms as well as materials,are formed of molecules and of the organized entities resulting from the interaction of molecules with each other.Chemistry provides the bridge between the molecules of inanimate matter and the highly complex molecular architectures and systems which make up living organisms. Synthetic chemistry has developed a very powerful set of methods for constructing ever more complex molecules.Supramolecular chemistry seeks to con...

  15. Coordination Chemistry in Water of a Free and a Lipase-Embedded Cationic NCN-Pincer Platinum Center with Neutral and Ionic Triarylphosphines

    NARCIS (Netherlands)

    Wieczorek, B.; Snelders, D.J.M.; Dijkstra, H.P.; Versluis, C.; Lutz, M.; Spek, A.L.; Egmond, M.R.; Klein Gebbink, R.J.M.; van Koten, G.

    2012-01-01

    The coordination chemistry in aqueous media was studied for the platinum center of low-molecular-weight cationic NCN-pincer platinum complexes [RC6H2(CH2NMe2)2-3,5-Pt(H2O)-4]+ (R = −(CH2)3P(═O)(OEt)(OC6H4NO2-4) (1(OH2)), H (2(OH2))) as well as of the platinum center of the NCN-pincer platinum cation

  16. Constitutional dynamic chemistry: bridge from supramolecular chemistry to adaptive chemistry.

    Science.gov (United States)

    Lehn, Jean-Marie

    2012-01-01

    Supramolecular chemistry aims at implementing highly complex chemical systems from molecular components held together by non-covalent intermolecular forces and effecting molecular recognition, catalysis and transport processes. A further step consists in the investigation of chemical systems undergoing self-organization, i.e. systems capable of spontaneously generating well-defined functional supramolecular architectures by self-assembly from their components, thus behaving as programmed chemical systems. Supramolecular chemistry is intrinsically a dynamic chemistry in view of the lability of the interactions connecting the molecular components of a supramolecular entity and the resulting ability of supramolecular species to exchange their constituents. The same holds for molecular chemistry when the molecular entity contains covalent bonds that may form and break reversibility, so as to allow a continuous change in constitution by reorganization and exchange of building blocks. These features define a Constitutional Dynamic Chemistry (CDC) on both the molecular and supramolecular levels.CDC introduces a paradigm shift with respect to constitutionally static chemistry. The latter relies on design for the generation of a target entity, whereas CDC takes advantage of dynamic diversity to allow variation and selection. The implementation of selection in chemistry introduces a fundamental change in outlook. Whereas self-organization by design strives to achieve full control over the output molecular or supramolecular entity by explicit programming, self-organization with selection operates on dynamic constitutional diversity in response to either internal or external factors to achieve adaptation.The merging of the features: -information and programmability, -dynamics and reversibility, -constitution and structural diversity, points to the emergence of adaptive and evolutive chemistry, towards a chemistry of complex matter.

  17. Green chemistry: A tool in Pharmaceutical Chemistry

    Directory of Open Access Journals (Sweden)

    Smita Talaviya

    2012-07-01

    Full Text Available Green chemistry expresses an area of research developing from scientific discoveries about pollution awareness and it utilizes a set of principles that reduces or eliminates the use or generation of hazardous substances in all steps of particular synthesis or process. Chemists and medicinal scientists can greatly reduce the risk to human health and the environment by following all the valuable principles of green chemistry. The most simple and direct way to apply green chemistry in pharmaceuticals is to utilize eco-friendly, non-hazardous, reproducible and efficient solvents and catalysts in synthesis of drug molecules, drug intermediates and in researches involving synthetic chemistry. Microwave synthesis is also an important tool of green chemistry by being an energy efficient process.

  18. Environmental chemistry: Volume A

    Energy Technology Data Exchange (ETDEWEB)

    Yen, T.F.

    1999-08-01

    This is an extensive introduction to environmental chemistry for engineering and chemical professionals. The contents of Volume A include a brief review of basic chemistry prior to coverage of litho, atmo, hydro, pedo, and biospheres.

  19. Advanced Chemistry Laboratory

    Data.gov (United States)

    Federal Laboratory Consortium — Description/History: Chemistry laboratoryThe Advanced Chemistry Laboratory (ACL) is a unique facility designed for working with the most super toxic compounds known...

  20. Organometallic Chemistry of Molybdenum.

    Science.gov (United States)

    Lucas, C. Robert; Walsh, Kelly A.

    1987-01-01

    Suggests ways to avoid some of the problems students have learning the principles of organometallic chemistry. Provides a description of an experiment used in a third-year college chemistry laboratory on molybdenum. (TW)

  1. Chemistry for Potters.

    Science.gov (United States)

    Denio, Allen A.

    1980-01-01

    Relates pottery making to chemistry by providing chemical information about clay, its origin, composition, properties, and changes that occur during firing; also describes glaze compositions, examples of redox chemistry, salt glazing, crystalline glazes, and problems in toxicity. (CS)

  2. CHINESE JOURNAL OF CHEMISTRY

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    @@Chinese Journal of Chemistry is an international journal published in English by the Chinese Chemical Society with its editorial office hosted by Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences.

  3. Amine chemistry. Update on impact on resin

    Energy Technology Data Exchange (ETDEWEB)

    Bachman, Gregory; Kellogg, Douglas [Siemens Industry, Inc., Rockford, IL (United States). Technology and Lab Services; Wilkes, Marty [Siemens Industry, Inc., Rockford, IL (United States). Water Technologies Div.

    2012-03-15

    Impurity removal in the steam cycle and the associated prevention of corrosion and/or fouling of system components are the goals of ion exchange resins. However, in many instances (such as a switch to amine chemistry or a change in product specifications), resins do not remove, and, in fact, contribute impurities to the steam cycle. This paper reviews recent data compiled to determine the direct and indirect effects of amines on ion exchange resins used in the power industry. Water chemistries have improved in recent years, in large part due to changes in chemistry and resins, but it is necessary to continue to develop products, processes and techniques to reduce impurities and improve overall water chemistry in power plant systems. (orig.)

  4. Organic chemistry experiment

    Energy Technology Data Exchange (ETDEWEB)

    Mun, Seok Sik

    2005-02-15

    This book deals with organic chemistry experiments, it is divided five chapters, which have introduction, the way to write the experiment report and safety in the laboratory, basic experiment technic like recrystallization and extraction, a lot of organic chemistry experiments such as fischer esterification, ester hydrolysis, electrophilic aromatic substitution, aldol reaction, benzoin condensation, wittig reaction grignard reaction, epoxidation reaction and selective reduction. The last chapter introduces chemistry site on the internet and way to find out reference on chemistry.

  5. Green Chemistry and Education.

    Science.gov (United States)

    Hjeresen, Dennis L.; Schutt, David L.; Boese, Janet M.

    2000-01-01

    Many students today are profoundly interested in the sustainability of their world. Introduces Green Chemistry and its principles with teaching materials. Green Chemistry is the use of chemistry for pollution prevention and the design of chemical products and processes that are environmentally benign. (ASK)

  6. Understanding the molecular-level chemistry of water plasmas and the effects of surface modification and deposition on a selection of oxide substrates

    Science.gov (United States)

    Trevino, Kristina J.

    2011-12-01

    This dissertation first examines electrical discharges used to study wastewater samples for contaminant detection and abatement. Two different water samples contaminated with differing concentrations of either methanol (MeOH) or methyl tert-butyl ether (MTBE) were used to follow breakdown mechanisms. Emission from CO* was used to monitor the contaminant and for molecular breakdown confirmation through actinometric OES as it can only arise from the carbon-based contaminant in either system. Detection was achieved at concentrations as low as 0.01 ppm, and molecular decomposition was seen at a variety of plasma parameters. This dissertation also explores the vibrational (thetaV), rotational (thetaR) and translational (thetaT) temperatures for a range of diatomic species in different plasma systems. For the majority of the plasma species studied, thetaV are much higher than thetaR and thetaT. This suggests that more energy is partitioned into the vibrational degrees of freedom in our plasmas. The thetaR reported are significantly lower in all the plasma systems studied and this is a result of radical equilibration to the plasma gas temperature. thetaT values show two characteristics; (1) they are less than the thetaV and higher than the theta R and (2) show varying trends with plasma parameters. Radical energetics were examined through comparison of thetaR, thetaT, and thetaV, yielding significant insight on the partitioning of internal and kinetic energies in plasmas. Correlations between energy partitioning results and corresponding radical surface scattering coefficients obtained using our imaging of radicals interacting with surfaces (IRIS) technique are also presented. Another aspect of plasma process chemistry, namely surface modification via plasma treatment, was investigated through characterization of metal oxides (SiOxNy, nat-SiO2, and dep-SiO2) following their exposure to a range of plasma discharges. Here, emphasis was placed on the surface wettability

  7. The chemistry of subcritical water reactions of a hardwood derived lignin and lignin model compounds with nitrogen, hydrogen, carbon monoxide and carbon dioxide

    Science.gov (United States)

    Hill Bembenic, Meredith A.

    Biofuels, like cellulosic ethanol, may only be cost effective if the lignin byproduct is upgraded to value-added products. However, lignin's inherent aromatic structure and interunit crosslinkages hinder effective conversion. High temperature H2O is considered for lignin conversion, because H2O exhibits unusual properties at higher temperatures (particularly at its supercritical point of 374°C and 3205 psi) including a decreased ion product and a decreased static dielectric constant (similar to those of polar organic solvents at room temperature) such that there is a high solubility for organic compounds, like lignin. Much of the research concerning lignin and supercritical H2O has focused on further decomposition to gases (e.g., H2, CH4, and CO2) where nearly no char formation is expected in the presence of a catalyst. However, the conditions required for supercritical H2O are difficult to maintain, catalysts can be expensive, and gases are not favorable to the current liquid fuel infrastructure. Reactions using Organosolv lignin, subcritical H2O (365°C) and various industrial gases (N2, H2, CO, and CO2 at an initial pressure of 500 psi) for 30 min. were examined to determine both lignin's potential to generate value-added products (e.g., monomer compounds and methanol) and the role (if any) of the H2O and the gases during the reactions. The behavior of H2O at reaction temperature and pressure is expected to be similar to the behavior of supercritical H 2O without the need to maintain supercritical conditions. Different characterization techniques were used for the products collected including primarily GC/FID-TCD of the evolved gases, GC/MS analysis of the organic liquids, solid phase microextraction analysis of the water, and solid state 13C-NMR analysis of the residues. The reactor pressure at temperature was shown to influence the reactivity of the H2O and lignin, and the highest conversions (≈54--62%) were obtained when adding a gas. However, the

  8. In-Package Chemistry Abstraction

    Energy Technology Data Exchange (ETDEWEB)

    E. Thomas

    2004-11-09

    This report was developed in accordance with the requirements in ''Technical Work Plan for: Regulatory Integration Modeling and Analysis of the Waste Form and Waste Package'' (BSC 2004 [DIRS 171583]). The purpose of the in-package chemistry model is to predict the bulk chemistry inside of a breached waste package and to provide simplified expressions of that chemistry as function of time after breach to Total Systems Performance Assessment for the License Application (TSPA-LA). The scope of this report is to describe the development and validation of the in-package chemistry model. The in-package model is a combination of two models, a batch reactor model that uses the EQ3/6 geochemistry-modeling tool, and a surface complexation model that is applied to the results of the batch reactor model. The batch reactor model considers chemical interactions of water with the waste package materials and the waste form for commercial spent nuclear fuel (CSNF) waste packages and codisposed waste packages that contain both high-level waste glass (HLWG) and DOE spent fuel. The surface complexation model includes the impact of fluid-surface interactions (i.e., surface complexation) on the resulting fluid composition. The model examines two types of water influx: (1) the condensation of water vapor that diffuses into the waste package, and (2) seepage water that enters the waste package from the drift as a liquid. (1) Vapor Influx Case: The condensation of vapor onto the waste package internals is simulated as pure H2O and enters at a rate determined by the water vapor pressure for representative temperature and relative humidity conditions. (2) Water Influx Case: The water entering a waste package from the drift is simulated as typical groundwater and enters at a rate determined by the amount of seepage available to flow through openings in a breached waste package. TSPA-LA uses the vapor influx case for the nominal scenario for simulations where the waste

  9. Synthesis and Coordination Chemistry of a Phosphine-Decorated Fluorescein: "Double Turn-On" Sensing of Gold(III) Ions in Water.

    Science.gov (United States)

    Christianson, Anna M; Gabbaï, François P

    2016-06-20

    Although phosphine ligands are ubiquitous in transition metal chemistry, few reports of fluorescent phosphines exist that explore the effect of metal coordination on the photophysical properties of a phosphine-bound fluorescent group. The coordination chemistry of a derivative of fluorescein decorated with an o-phenylene-linked phosphine group has been studied with late transition metals. An Au(I) complex of the phosphine-decorated fluorescein has been structurally characterized, showing that the metal center is held closely over the plane of the fluorophore. Despite the presence of the heavy metal center, however, the phosphine-gold complex displays greatly increased fluorescence compared to the free ligand, in which photoelectron transfer from the lone-pair-bearing phosphine causes low emission. The phosphine-decorated fluorescein ligand was tested in a simple sensing system for metal ions in aqueous solution and shows a "turn-on" response to Au, Ag, and Hg, with an especially dramatic response to Au(III) species. The selectivity for Au(III) was determined to be the result of a "double turn-on" response that is both reaction- and coordination-based.

  10. Surface chemistry essentials

    CERN Document Server

    Birdi, K S

    2013-01-01

    Surface chemistry plays an important role in everyday life, as the basis for many phenomena as well as technological applications. Common examples range from soap bubbles, foam, and raindrops to cosmetics, paint, adhesives, and pharmaceuticals. Additional areas that rely on surface chemistry include modern nanotechnology, medical diagnostics, and drug delivery. There is extensive literature on this subject, but most chemistry books only devote one or two chapters to it. Surface Chemistry Essentials fills a need for a reference that brings together the fundamental aspects of surface chemistry w

  11. The New Color of Chemistry: Green Chemistry

    Directory of Open Access Journals (Sweden)

    Zuhal GERÇEK

    2012-01-01

    Full Text Available Green chemistry which is the new application of chemistry rules provides solutions to problems that mankind is faced with climate changes, sustainable agriculture, energy, toxics, depletion of natural sources e.g. designing new chemicals and processes that production and utilization of hazardous matters. So, it is the indispensible tool for sustainable development. Current and future chemists should consider the human health and ecological issues in their professional life. In order to provide a solution for this requirement, green chemistry rules and under standings should be primarily taken in the university curriculum and at all educational levels.

  12. Hydrogeology and Water Quality of the Pepacton Reservoir Watershed in Southeastern New York. Part 3. Responses of Stream Base-Flow Chemistry to Hydrogeologic Factors and Nonpoint-Sources of Contamination

    Science.gov (United States)

    Heisig, Paul M.; Phillips, Patrick J.

    2004-01-01

    quality, and stream base-flow water quality. Chloride and sodium, which are relatively conservative constituents, showed strong linear relations with annual estimates of road-salt application during all four sampling periods. Nonconservative constituents, such as the nutrients nitrate and orthophosphate, showed linear relations with manure production rate among farmed basins, but only at specific times of the year because of losses through biologic activity. Nitrate showed the strongest relation in winter because losses to biological activity were at a minimum. Orthophosphate showed the strongest relation in early summer, when hydrologic and chemical conditions appear to favor release from sediments. Atmospheric nitrogen deposition is an additional source of nitrogen that can be released from mature or stressed forested basins. Detections of herbicides (atrazine, metolachlor, simazine) and herbicide degradates ( Metolachlor ESA, alachlor ESA, deethylatrazine) in base flow were closely correlated with subbasins in which corn was grown during the study. Atrazine was detected at the farmed index site only in early summer, after application and two rain storms. This detection corresponded to the peak orthophosphate concentration. In contrast, metolachlor ESA was detected in nearly all farmedindex- subbasin samples and peaked in late summer, when percent base-flow contributions from farmed valley-bottom areas were likely highest. The implications of this study are that seasonal and more frequent base-flow surveys of water chemistry from small stream basins can help refine the understanding of local hydrogeologic systems and define the effects of nonpointsource contamination on base-flow water quality. The concentration of most nonpoint sources in valley-bottom or lower-hillside areas helped indicate the relative contributions of water from hillside and valley-bottom areas at different times of year. The positive correlations between the intensity of nonpoint-

  13. Geohydrology and water chemistry of abandoned uranium mines and radiochemistry of spoil-material leachate, Monument Valley and Cameron areas, Arizona and Utah

    Science.gov (United States)

    Longsworth, S.A.

    1994-01-01

    Uranium mines in the Monument Valley area were established predominately in channel-fill deposits within the Shinarump Member of the Chinle Formation. The Shinarump Member yields ground water to wells and may yield water to the Moonlight and Radium Hill mines. In the study area near Cameron, uranium was mined from channel-fill deposits within the Petrified Forest Member of the Chinle Formation. Units of the Petrified Forest Member do not yield ground water to wells in the area, but fractures in the lower part of the Petrified Forest Member are probable pathways for upward flow of water from the Shinarump Member. Most of the mines receive water from surface inflow of rainfall runoff, but ground water also may be transmitted to open pits and drill holes in the subsurface through fractures or along faults in the Petrified Forest Member. Uranium-238 activities in shallow ground water from mines ranged from 150 to 14,000 picocuries per liter. Radionuclide activities in well and spring water were less than in shallow ground water near mines; however, in some samples, radionuclide activities in wells and springs were greater than activities in pit water. Uranium concentrations in leachate samples ranged from 20 to 7,700 micrograms per liter. Batch tests were done with material that was 2.00 millimeters and smaller. The radiochemistry of leachate from coarser material was not determined, and the specific rate and magnitude of radionuclide leaching depends on site-specific conditions that include the amounts of oxygen and organic material present, temperature, spoil mineralogy, and local ground-water composition.

  14. Developing and Implementing Inquiry-Based, Water Quality Laboratory Experiments for High School Students to Explore Real Environmental Issues Using Analytical Chemistry

    Science.gov (United States)

    Mandler, Daphna; Blonder, Ron; Yayon, Malka; Mamlok-Naaman, Rachel; Hofstein, Avi

    2014-01-01

    This paper describes the rationale and the implementation of five laboratory experiments; four of them, intended for high-school students, are inquiry-based activities that explore the quality of water. The context of water provides students with an opportunity to study the importance of analytical methods and how they influence our everyday…

  15. Evaluation of isotope migration: land burial. Water chemistry at commercially operated low-level radioactive waste disposal sites. Progress report No. 7, October--December 1977

    Energy Technology Data Exchange (ETDEWEB)

    Colombo, P.; Weiss, A. J.; Francis, A. J.

    1978-01-01

    Trench water samples from the commercial low-level radioactive waste disposal sites at Maxey Flats, Kentucky, and West Valley, New York, were collected, and the bacterial populations were enumerated. The range of bacterial populations in six trench water samples were 400 to 24,000 aerobic and 90 to 15,000 anaerobic bacteria/ml. Most of the bacteria isolated from the anaerobic culture plates were facultative anaerobes, although a few strict anaerobes were also present. Mixed bacterial populations isolated from the trench waters were able to grow anaerobically utilizing the carbon and nitrogen sources present in the trench waters. Trench waters supplemented with mineral salts supported only a modest increase in growth of these bacteria. The results of this study indicate that bacteria are active in the trenches, and the radioactivity and organic compounds present in the trenches are not toxic to these bacteria.

  16. The problem of optimizing the water chemistry used in the primary coolant circuit of a nuclear power station equipped with VVER reactors under the conditions of longer fuel cycle campaigns and increased capacity of power units

    Science.gov (United States)

    Sharafutdinov, R. B.; Kharitonova, N. L.

    2011-05-01

    It is shown that the optimal water chemistry of the primary coolant circuit must be substantiated while introducing measures aimed at increasing the power output in operating power units and for the project called AES-2006/AES TOI (a typical optimized project of a nuclear power station with enhanced information support). The experience gained from operation of PWR reactors with an elongated fuel cycle at an increased level of power is analyzed. Conditions under which boron compounds are locally concentrated on the fuel rod surfaces (the hideout phenomenon) and axial offset anomaly occurs are enlisted, and the influence of lithium on the hideout in the pores of deposits on the surfaces of fuel assemblies is shown.

  17. The New Color of Chemistry: Green Chemistry

    OpenAIRE

    Zuhal GERÇEK

    2012-01-01

    Green chemistry which is the new application of chemistry rules provides solutions to problems that mankind is faced with climate changes, sustainable agriculture, energy, toxics, depletion of natural sources e.g. designing new chemicals and processes that production and utilization of hazardous matters. So, it is the indispensible tool for sustainable development. Current and future chemists should consider the human health and ecological issues in their professional life. In order to provid...

  18. Enhancing resistance to burnout via coolant chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Tu, J. P.; Dinh, T. N.; Theofanous, T. G. [Univ. of California, Santa Barbara (United States)

    2003-07-01

    Boiling Crisis (BC) on horizontal, upwards-facing copper and steel surfaces under the influence of various coolant chemistries relevant to reactor containment waters is considered. In addition to Boric Acid (BA) and TriSodium Phosphate (TSP), pure De-Ionized Water (DIW) and Tap Water (TW) are included in experiments carried out in the BETA facility. The results are related to a companion paper on the large scale ULPU facility.

  19. Improvement of chemical monitoring of water-chemistry conditions at thermal power stations based on electric conductivity and pH measurements

    Science.gov (United States)

    Larin, A. B.; Larin, B. M.

    2016-05-01

    The increased requirements to the quality of the water heat conductor for working superhigh (SHP) and supercritical (SCP) pressure power plants and promising units, including combined-cycle gas turbine (CCGT) units and power plants with ultrasupercritical parameters (USCPs), can largely be satisfied through specific electric conductivity and pH measurements for cooled heat conductor samples combined with calculations of ionic equilibria and indirect measurements of several specified and diagnostic parameters. The possibility of calculating the ammonia and chloride concentrations and the total concentration of hardness and sodium cations in the feed water of drum-type boilers and the phosphate and salt contents in boiler water was demonstrated. An equation for evaluating the content of potentially acid substances in the feed water of monotube boilers was suggested. The potential of the developed procedure for evaluating the state of waterchemistry conditions (WCCs) in power plants with CCGT units was shown.

  20. The chemistry and isotopic composition of waters in the low-enthalpy geothermal system of Cimino-Vico Volcanic District, Italy

    DEFF Research Database (Denmark)

    Battistel, Maria; Hurwitz, Shaul; Evans, William C.

    2016-01-01

    a lack of hydraulic continuity across the region. The δ18O (− 6.6‰ to − 5.9‰) and δD (− 40.60‰ to − 36.30‰) isotopic composition of spring water suggest that the recharge area for the geothermal system is the summit region of Mount Cimino. The strontium isotope ratios (87Sr/86Sr) of thermal waters (0...

  1. Concrete durability: physical chemistry of the water attack; Durabilite du beton: physico-chimie de l`alteration par l`eau

    Energy Technology Data Exchange (ETDEWEB)

    Faucon, P.

    1997-01-22

    Cement paste constitutes an basic medium, thermodynamically stable for high pH`s. For this reason, water constitutes an aggressive environment. For hydraulic structures, or nuclear waste disposal, water must be considered as a `chemical loading`. In the short- and medium-term water-degradation of cement paste is principally due to transport of matter between the healthy zone and the aggressive solution through diffusion of ionic species from the interstitial solution of the cement paste. In the long-term, dissolution of the surface may occur. Various cement pastes were prepared and leached with continually demineralized water. After a critical time, which depends on the type of paste, the dissolution of the surface layer in contact with water will control the degradation kinetics. The diffusive and chemical properties of the degraded layer are therefore fundamental for the prediction of the long-term behaviour of concrete in water. {sup 29}Si Magic Angle Spinning Nuclear Magnetic Resonance (MAS NMR) combined with {sup 27}A1 MAS NMR and {sup 57}Fe Moessbauer spectroscopy indicate that the superficial layer is formed by a CSH with a molecular structure near from the tobermorite mineral. Nuclear magnetic resonance techniques allow us to demonstrate the fundamental role of cationic substitutions occurring in the CSH during degradation on the superficial layer solubility. Our experimental results were used to model the cement paste behaviour taking into account the diffusion and the dissolution of the material. (author).

  2. Twenty-year inter-annual trends and seasonal variations in precipitation and stream water chemistry at the Bear Brook Watershed in Maine, USA.

    Science.gov (United States)

    Navrátil, Tomas; Norton, Stephen A; Fernandez, Ivan J; Nelson, Sarah J

    2010-12-01

    Mean annual concentration of SO4(-2) in wet-only deposition has decreased between 1988 and 2006 at the paired watershed study at Bear Brook Watershed in Maine, USA (BBWM) due to substantially decreased emissions of SO(2). Emissions of NO(x) have not changed substantially, but deposition has declined slightly at BBWM. Base cations, NH4+, and Cl(-) concentrations were largely unchanged, with small irregular changes of <1 μeq L(-1) per year from 1988 to 2006. Precipitation chemistry, hydrology, vegetation, and temperature drive seasonal stream chemistry. Low flow periods were typical in June-October, with relatively greater contributions of deeper flow solutions with higher pH; higher concentrations of acid-neutralizing capacity, Si, and non-marine Na; and low concentrations of inorganic Al. High flow periods during November-May were typically dominated by solutions following shallow flow paths, which were characterized by lower pH and higher Al and DOC concentrations. Biological activity strongly controlled NO3- and K(+). They were depressed during the growing season and elevated in the fall. Since 1987, East Bear Brook (EB), the reference stream, has been slowly responding to reduced but still elevated acid deposition. Calcium and Mg have declined fairly steadily and faster than SO4(-2), with consequent acidification (lower pH and higher inorganic Al). Eighteen years of experimental treatment with (NH(4))(2)SO(4) enhanced acidification of West Bear Brook's (WB) watershed. Despite the manipulation, NH4+ concentration remained below detection limits at WB, while leaching of NO3- increased. The seasonal pattern for NO3- concentrations in WB, however, remained similar to EB. Mean monthly concentrations of SO4(-2) have increased in WB since 1989, initially only during periods of high flow, but gradually also during base flow. Increases in mean monthly concentrations of Ca(2+), Mg(2+), and K(+) due to the manipulation occurred from 1989 until about 1995, during the

  3. Orbital interactions in chemistry

    CERN Document Server

    Albright, Thomas A; Whangbo, Myung-Hwan

    2013-01-01

    Explains the underlying structure that unites all disciplines in chemistry Now in its second edition, this book explores organic, organometallic, inorganic, solid state, and materials chemistry, demonstrating how common molecular orbital situations arise throughout the whole chemical spectrum. The authors explore the relationships that enable readers to grasp the theory that underlies and connects traditional fields of study within chemistry, thereby providing a conceptual framework with which to think about chemical structure and reactivity problems. Orbital Interactions

  4. Hydrogeologic Investigation, Water Chemistry Analysis, and Model Delineation of contributing Areas for City of Tallahassee Public-Supply Wells, Tallahassee, Florida

    Science.gov (United States)

    Davis, J. Hal; Katz, Brian G.

    2007-01-01

    Ground water from the Upper Floridan aquifer is the sole source of water supply for Tallahassee, Florida, and the surrounding area. The City of Tallahassee (the City) currently operates 28 water-supply wells; 26 wells are distributed throughout the City and 2 are located in Woodville, Florida. Most of these wells yield an ample supply of potable water; however, water from several wells has low levels of tetrachloroethylene (PCE). The City removes the PCE from the water by passing it through granular-activated carbon units before distribution. To ensure that water-supply wells presently free of contamination remain clean, it is necessary to understand the ground-water flow system in sufficient detail to protect the contributing areas. Ground-water samples collected from four public-supply wells were analyzed for tritium (3H), chlorofluorocarbons (CFCs), and sulfur hexafluoride (SF6). Using data for the CFC compounds, apparent ground-water ages ranged from 7 to 31 years. For SF6, the apparent ages tended to be about 5 to 10 years younger than those from CFCs. Apparent ages based on the tritium/tritiogenic helium-3 (3H/3Hetrit) method ranged from 26 to 33 years. The three dating methods indicate that the apparent age of ground water generally decreases from northern to southern Leon County. This southward trend of decreasing ages is consistent with increasing amounts of recharge that occur as ground water moves from north to south. The ground-water age data derived by geochemical and tracer analyses were used in combination with the flow model and particle tracking to determine an effective porosity for the Hawthorn clays and Upper Floridan aquifer. The effective porosities for the Upper Floridan aquifer that resulted in best model matches were averaged to produce an effective porosity of 7 percent, and the effective porosities for the Hawthorn clays that resulted in a match were averaged to produce an effective porosity of 22 percent. Probabilistic contributing areas

  5. Chemistry of fog waters in California's Central Valley - Pt. 3: concentrations and speciation of organic and inorganic nitrogen

    Energy Technology Data Exchange (ETDEWEB)

    Qi Zhang; Anastasio, C. [University of California, Davis, CA (United States). Atmospheric Science Program, Department of Land, Air and Water Resources

    2001-07-01

    Although organic nitrogen (ON) has been found to be a ubiquitous and significant component in wet and dry deposition, almost nothing is known about its concentration or composition in fog waters. To address this gap, we have investigated the concentration and composition of ON in fog waters collected in Davis, in California's Central Valley. Significant quantities of dissolved organic nitrogen (DON) were found in these samples, with a median concentration of 303{mu}M N (range=120-1630{mu}M N). DON typically represented approximately 16% of the total dissolved nitrogen (inorganic+organic) in Davis fog waters. The median concentration of nitrogen in free amino acids and alkyl amines was 16{mu}M N (range=3.8-120{mu}M N), which accounted for 3.4% of the DON in Davis fogs. Thus, although the absolute concentrations of free amino compounds were significant, they were only a minor component of the DON pool. Combined amino nitrogen (e.g., proteins and peptides) was present at higher concentrations and accounted for 6.1-29 per cent (median=16%) of DON. Overall, free and combined amino compounds typically accounted for a median value of 22% of DON in the fog waters. The high concentrations of DON found, and the fact that amino and other N-containing organic compounds can serve as nitrogen sources for microorganisms and plants, indicate that atmospheric ON compounds likely play an important role in nitrogen cycling in the Central Valley. In addition, due to the basicity of some N functional groups, ON compounds likely contribute to the previously observed acid buffering capacity of Central Valley fog waters. Finally, a comparison of fog waters with fine particles (PM{sub 2.5}) collected from the same site during the same period of time indicated that the median concentrations (mol Nm{sup -3}-air) of total water-soluble ON, free amino nitrogen and total amino nitrogen were very similar in the fog water and PM{sub 2.5}. Given the high water solubility of many organic N

  6. Group theory and chemistry

    CERN Document Server

    Bishop, David M

    1993-01-01

    Group theoretical principles are an integral part of modern chemistry. Not only do they help account for a wide variety of chemical phenomena, they simplify quantum chemical calculations. Indeed, knowledge of their application to chemical problems is essential for students of chemistry. This complete, self-contained study, written for advanced undergraduate-level and graduate-level chemistry students, clearly and concisely introduces the subject of group theory and demonstrates its application to chemical problems.To assist chemistry students with the mathematics involved, Professor Bishop ha

  7. Green Chemistry Pedagogy

    Science.gov (United States)

    Kolopajlo, Larry

    2017-02-01

    This chapter attempts to show how the practice of chemistry teaching and learning is enriched by the incorporation of green chemistry (GC) into lectures and labs. To support this viewpoint, evidence from a wide range of published papers serve as a cogent argument that GC attracts and engages both science and nonscience students, enhances chemistry content knowledge, and improves the image of the field, while preparing the world for a sustainable future. Published pedagogy associated with green and sustainable chemistry is critically reviewed and discussed.

  8. Advances in quantum chemistry

    CERN Document Server

    Sabin, John R

    2013-01-01

    Advances in Quantum Chemistry presents surveys of current topics in this rapidly developing field that has emerged at the cross section of the historically established areas of mathematics, physics, chemistry, and biology. It features detailed reviews written by leading international researchers. This volume focuses on the theory of heavy ion physics in medicine.Advances in Quantum Chemistry presents surveys of current topics in this rapidly developing field that has emerged at the cross section of the historically established areas of mathematics, physics, chemistry, and biology. It features

  9. Science Update: Analytical Chemistry.

    Science.gov (United States)

    Worthy, Ward

    1980-01-01

    Briefly discusses new instrumentation in the field of analytical chemistry. Advances in liquid chromatography, photoacoustic spectroscopy, the use of lasers, and mass spectrometry are also discussed. (CS)

  10. Water

    Science.gov (United States)

    Leopold, Luna Bergere; Baldwin, Helene L.

    1962-01-01

    What do you use water for?If someone asked you this question you would probably think right away of water for drinking. Then you would think of water for bathing, brushing teeth, flushing the toilet. Your list would get longer as you thought of water for cooking, washing the dishes, running the garbage grinder. Water for lawn watering, for play pools, for swimming pools, for washing the car and the dog. Water for washing machines and for air conditioning. You can hardly do without water for fun and pleasure—water for swimming, boating, fishing, water-skiing, and skin diving. In school or the public library, you need water to wash your hands, or to have a drink. If your home or school bursts into flames, quantities of water are needed to put it out.In fact, life to Americans is unthinkable without large supplies of fresh, clean water. If you give the matter a little thought, you will realize that people in many countries, even in our own, may suffer from disease and dirt simply because their homes are not equipped with running water. Imagine your own town if for some reason - an explosion, perhaps - water service were cut off for a week or several weeks. You would have to drive or walk to a neighboring town and bring water back in pails. Certainly if people had to carry water themselves they might not be inclined to bathe very often; washing clothes would be a real chore.Nothing can live without water. The earth is covered by water over three-fourths of its surface - water as a liquid in rivers, lakes and oceans, and water as ice and snow on the tops of high mountains and in the polar regions. Only one-quarter of our bodies is bone and muscle; the other three-fourths is made of water. We need water to live, and so do plants and animals. People and animals can live a long time without food, but without water they die in a few days. Without water, everything would die, and the world would turn into a huge desert.

  11. TOC in water/steam cycles. Zittau Colloquium on Power Plant Chemistry; TOC in Wasser/Dampf-Kreislaeufen. Zittauer Kraftwerkschemisches Kolloquium

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2000-07-01

    Many power plants use treated surface water as boiler feedwater and have difficulties in keeping within the limits for organic substances in feedwater (TOC < 200 ppb) or acid conductivity in steam condensate (< 0.2 {mu}S/cm). The characteristics of surface water and the role of organic substances in boiler feedwater are explained and discussed. [German] Viele Kraftwerke bereiten fuer die Erzeugung von Kesselspeisewasser Oberflaechenwasser auf und haben Probleme, die Richtlinien fuer organische Stoffe im Speisewasser (TOC < 200 ppb) oder Saeure-Leitfaehigkeit in Dampfkondensaten (< 0,2 {mu}S/cm) einzuhalten. Die besonderen Eigenschaften von Oberflaechenwaessern und die Bedeutung organischer Stoffe in Kesselspeisewasser werden erlaeutert und diskutiert. (orig.)

  12. Assessment of surface water chemistry and algale biodiversity in the Bay of Mostaganem and the Cheliff estuary: North-western Algeria

    OpenAIRE

    Fatima kies

    2015-01-01

    Anthropogenic activities have led to water quality deterioration in many parts of the word, especially in Northwest Algeria. The current work investigated the spatiotemporal variations of water quality in the Cheliff River, samples for physico-chemical were performed at different periods from 2004 to 2007, the results chowed that nitrate (NO3-) intake is very high especially in the month of February 2006 (26 mg/l) and February 2007 (37 mg/l), nitrite (NO2-) values also exceed the standard fo...

  13. Catalysis in the Service of Green Chemistry: Nobel Prize-Winning Palladium-Catalysed Cross-Couplings, Run in Water at Room Temperature

    Science.gov (United States)

    Lipshutz, Bruce H.; Taft, Benjamin R.; Abela, Alexander R.; Ghorai, Subir; Krasovskiy, Arkady; Duplais, Christophe

    2012-01-01

    Palladium-catalysed cross-couplings, in particular Heck, Suzuki-Miyaura and Negishi reactions developed over three decades ago, are routinely carried out in organic solvents. However, alternative media are currently of considerable interest given an increasing emphasis on making organic processes ‘greener’; for example, by minimising organic waste in the form of organic solvents. Water is the obvious leading candidate in this regard. Hence, this review focuses on the application of micellar catalysis, in which a ‘designer’ surfactant enables these award-winning coupling reactions to be run in water at room temperature. PMID:23555153

  14. Aqueous-phase chemistry and bactericidal effects from an air discharge plasma in contact with water: evidence for the formation of peroxynitrite through a pseudo-second-order post-discharge reaction of H2O2 and HNO2

    Science.gov (United States)

    Lukes, P.; Dolezalova, E.; Sisrova, I.; Clupek, M.

    2014-02-01

    The formation of transient species (OH·, NO2·, NO radicals) and long-lived chemical products (O3, H2O2, NO_{3}^{-} , NO_{2}^{-} ) produced by a gas discharge plasma at the gas-liquid interface and directly in the liquid was measured in dependence on the gas atmosphere (20% oxygen mixtures with nitrogen or with argon) and pH of plasma-treated water (controlled by buffers at pH 3.3, 6.9 or 10.1). The aqueous-phase chemistry and specific contributions of these species to the chemical and biocidal effects of air discharge plasma in water were evaluated using phenol as a chemical probe and bacteria Escherichia coli. The nitrated and nitrosylated products of phenol (4-nitrophenol, 2-nitrophenol, 4-nitrocatechol, 4-nitrosophenol) in addition to the hydroxylated products (catechol, hydroquinone, 1,4-benzoquinone, hydroxy-1,4-benzoquinone) evidenced formation of NO2·, NO· and OH· radicals and NO+ ions directly by the air plasma at the gas-liquid interface and through post-discharge processes in plasma-activated water (PAW) mediated by peroxynitrite (ONOOH). Kinetic study of post-discharge evolution of H2O2 and NO_{2}^{-} in PAW has demonstrated excellent fit with the pseudo-second-order reaction between H2O2 and NO_{2}^{-} . The third-order rate constant k = 1.1 × 103 M-2 s-1 for the reaction NO_{2}^{-} +H_{2}O_{2}+H^{+}\\to ONOOH+H_{2}O was determined in PAW at pH 3.3 with the rate of ONOOH formation in the range 10-8-10-9 M s-1. Peroxynitrite chemistry was shown to significantly participate in the antibacterial properties of PAW. Ozone presence in PAW was proved indirectly by pH-dependent degradation of phenol and detection of cis,cis-muconic acid, but contribution of ozone to the inactivation of bacteria by the air plasma was negligible.

  15. Water chemistry at Hontomín-Huermeces (Burgos, Spain): insights for a pre-, intra- and post-CO2 injection geochemical monitoring.

    Science.gov (United States)

    Nisi, Barbara; Vaselli, Orlando; Tassi, Franco; de Elio, Javier; Delgado Huertas, António; Mazadiego, Luis Felipe; Ortega, Marcelo F.

    2013-04-01

    In this study, the very first geochemical and isotopic data related to surface and spring waters and dissolved gases in the area of Hontomín-Huermeces (Burgos, Spain) are presented and discussed. Hontomín-Huermeces was selected as a pilot site for the injection of pure (>99 %) CO2. Injection and monitoring wells are planned to be drilled close to 6 oil wells completed in the 1980's. Stratigraphical logs indicate the presence of a confined saline aquifer at the depth of about 1,500 m into which less than 100,000 tons of liquid CO2 will be injected, possibly starting in 2013. The chemical and isotopic features of the spring waters suggest the occurrence of a shallow aquifer having a Ca2+(Mg2+)-HCO3- composition, relatively low salinity (Total Dissolved Solids ≈800 mg/L) and a meteoric isotopic signature. Some spring waters close to the oil wells are characterized by relatively high concentrations of NO3- (up to 123 mg/L), unequivocally indicating anthropogenic contamination that adds to the main water-rock interaction processes. The latter can be referred to Ca-Mg-carbonate and, at a minor extent, Al-silicate dissolution, being the outcropping sedimentary rocks characterized by Palaeozoic to Quaternary rocks. Anomalous concentrations of Cl-, SO42-, As, B and Ba were measured in two springs discharging a few hundreds meters from the oil wells and in the Rio Ubierna, possibly indicative of mixing processes, although at very low extent, between deep and shallow aquifers. Gases dissolved in spring waters show relatively high concentrations of atmospheric species, such as N2, O2 and Ar, and isotopically negative CO2 (migration of the injected CO2 into near-surface environments.

  16. Relationships between benthic macroinvertebrate community structure and geospatial habitat, in-stream water chemistry, and surfactants in the effluent-dominated Trinity River, Texas, USA.

    Science.gov (United States)

    Slye, Jaime L; Kennedy, James H; Johnson, David R; Atkinson, Sam F; Dyer, Scott D; Ciarlo, Michael; Stanton, Kathleen; Sanderson, Hans; Nielsen, Allen M; Price, Bradford B

    2011-05-01

    Over the past 20 years, benthic macroinvertebrate community structure studies have been conducted on the upper Trinity River, Texas, USA, which is dominated by municipal wastewater treatment plant (WWTP) and industrial effluents. The Trinity River is located in the Dallas-Fort Worth metropolitan area, and is the most highly populated and industrialized watershed in Texas. As such, the Trinity River represents a near-worst-case scenario to examine the environmental effects of domestic-municipal and industrial effluents on aquatic life. A 1987 to 1988 study concluded that many stretches of the river supported a diverse benthic community structure; however, a decline in taxa richness occurred immediately downstream of WWTPs. A 2005 study designed to parallel the 1987 to 1988 efforts evaluated how changes in water quality, habitat, and increased urbanization impacted benthic community structure. Physicochemical measurements, habitat quality, geospatial variables, and benthic macroinvertebrates were collected from 10 sites. Surfactants were measured and toxic units (TUs) were calculated for surface water and pore water as indicators of domestic/household use of cleaning products. Total TUs indicated a low potential for biological impacts. Toxic unit distribution was not dependent on WWTP location and did not correlate with any benthic variable. Eight environmental parameters were determined to be useful for predicting changes in benthic macroinvertebrate community structure: surfactant surface water TUs (SWTU), in-stream habitat cover, and surface water total organic carbon were the top three parameters. Abundance, taxa richness, and taxa similarity in 2005 had increased since the earlier study throughout the immediate vicinity of the metropolitan area.

  17. Water

    Science.gov (United States)

    ... Lead Poisoning Prevention Training Center (HHLPPTC) Training Tracks Water Language: English Español (Spanish) Recommend on Facebook Tweet Share Compartir For information about lead in water in Flint, MI, please visit http://www.phe. ...

  18. Computational chemistry at the petascale: Are we there yet?

    Science.gov (United States)

    Aprá, E.; Harrison, R. J.; Shelton, W. A.; Tipparaju, V.; Vázquez-Mayagoitia, A.

    2009-07-01

    We have run computational chemistry calculations approaching the Petascale level of performance (~ 0.5 PFlops). We used the Coupled Cluster CCSD(T) module of the computational chemistry code NWChem to evaluate accurate energetics of water clusters on a 1.4 PFlops Cray XT5 computer.

  19. River chemistry as a monitor of Yosemite Park mountain hydroclimates

    Science.gov (United States)

    Peterson, David; Smith, Richard; Hager, Stephen; Hicke, Jeffrey A.; Dettinger, Michael; Huber, King

    2005-01-01

    High-frequency, high-altitude measurements of water chemistry provide insights into processes relating to the hydrology, climate, and geochemistry of mountain catchments. When such observations are combined with stream stage, temperature, snow, weather, and other surface hydroclimate measurements, they are particularly useful in allowing connections between climate, river discharge, river chemistry, and ecosystems to be discerned.

  20. Aqueous Solution Chemistry on Mars

    Science.gov (United States)

    Quinn, R.; Hecht, M.; Kounaves, S.; Young, S.; West, S.; Fisher, A.; Grunthaner, P.

    2007-12-01

    Currently en route to Mars, the Phoenix mission carries four wet chemistry cells designed to perform basic solution chemistry on martian soil. The measurement objectives are typical of those that would be performed on an unknown sample on Earth, including detection of common anions and cations, total conductivity, pH, redox potential, cyclic voltammetry (CV), etc. Both the challenge and the novelty arise from the necessity to perform these measurements with severely constrained resources in a harsh and (literally) alien environment. Sensors for all measurements are integrated into a common "beaker," with the ability to perform a two-point calibration of some sensors using a pair of low-concentration solutions. Sulfate measurement is performed with a crude titration. While most measurements use ion selective electrodes, halide interferences are resolved by independent chronopotentiometry (CP) measurements. No preconditioning of the soil-water mixture is possible, nor is any physical characterization of the introduced soil sample beyond coarse visual inspection. Among the idiosyncrasies of the measurement is the low external pressure, which requires that the analysis be performed close to the boiling point of water under an atmosphere consisting almost entirely of water vapor. Despite these liabilities, however, extensive laboratory characterization has validated the basic approach, and protocols for both CV and CP have been developed and tested. Enhancing the value of the measurement is the suite of coordinated observations, such as microscopy and evolved gas analysis, to be performed by other Phoenix instruments.

  1. Chemistry in Microfluidic Channels

    Science.gov (United States)

    Chia, Matthew C.; Sweeney, Christina M.; Odom, Teri W.

    2011-01-01

    General chemistry introduces principles such as acid-base chemistry, mixing, and precipitation that are usually demonstrated in bulk solutions. In this laboratory experiment, we describe how chemical reactions can be performed in a microfluidic channel to show advanced concepts such as laminar fluid flow and controlled precipitation. Three sets of…

  2. Exercises in Computational Chemistry

    DEFF Research Database (Denmark)

    Spanget-Larsen, Jens

    2016-01-01

    A selection of HyperChem© PC-exercises in computational chemistry. Answers to most questions are appended (Roskilde University 2014-16).......A selection of HyperChem© PC-exercises in computational chemistry. Answers to most questions are appended (Roskilde University 2014-16)....

  3. Physical Chemistry of Molecular

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    @@ Established in 2009, the group consists of six researchers and more than 70 research assistants and graduate students from the CAS Key Laboratory of Molecular Nanostructures and Nanotechnologies at the CAS Institute of Chemistry.Its research focuses on the physical chemistry involved in molecular assembly, molecular nanostructures, functional nanomaterials and conceptual nano-devices.

  4. The Breath of Chemistry

    DEFF Research Database (Denmark)

    Josephsen, Jens

    The present preliminary text is a short thematic presentation in biological inorganic chemistry meant to illustrate general and inorganic (especially coordination) chemistry in biochemistry. The emphasis is on molecular models to explain features of the complicated mechanisms essential to breathing...

  5. Bioorganic and bioinorganic chemistry.

    Science.gov (United States)

    Constable, Edwin C; Housecroft, Catherine E; Creus, Marc; Gademann, Karl; Giese, Bernd; Ward, Thomas R; Woggon, Wolf D; Chougnet, Antoinette

    2010-01-01

    The interdisciplinary projects in bioinorganic and bioorganic chemistry of the Department of Chemistry, University of Basel led to the preparation of new systems that mimic biologically important processes and to the discovery of compounds from natural sources which are very promising with respect to medical applications. The advances in these areas are reported here.

  6. Mathematics and Chemistry

    Science.gov (United States)

    Henson, R.; Stumbles, A.

    1977-01-01

    The relationship between mathematics and chemistry has been changing rapidly in recent years. Some chemistry teachers have experienced difficulties in their teaching with the introduction of modern mathematics in the schools. Some suggestions for reinforcing the concepts and language of modern mathematics are put forth. (Author/MA)

  7. Chemistry of americium

    Energy Technology Data Exchange (ETDEWEB)

    Schulz, W.W.

    1976-01-01

    Essential features of the descriptive chemistry of americium are reviewed. Chapter titles are: discovery, atomic and nuclear properties, collateral reading, production and uses, chemistry in aqueous solution, metal, alloys, and compounds, and, recovery, separation, purification. Author and subject indexes are included. (JCB)

  8. Structure and intermolecular vibrations of 7-azaindole-water 2:1 complex in a supersonic jet expansion: Laser-induced fluorescence spectroscopy and quantum chemistry calculation

    Indian Academy of Sciences (India)

    Montu K Hazra; Moitrayee Mukherjee; V Ramanathan; Tapas Chakraborty

    2012-01-01

    Laser-induced fluorescence spectra of a 2:1 complex between 7-azaindole and water, known as `non-reactive dimer’ of the molecule, have been measured in a supersonic jet expansion. The dispersed fluorescence spectrum of the electronic origin band of the complex shows a very large number of low-frequency vibrational features corresponding to different intermolecular modes of the complex in the ground electronic state. Geometries of several possible isomeric structures of the complex and their vibrational frequencies at harmonic approximation were calculated by electronic structure theory method at MP2/6-31G∗∗ level. An excellent agreement is observed between the measured and calculated intermolecular vibrational mode frequencies for the energetically most favoured structure of the complex, where the water molecule is inserted within one of the two N$\\cdots$H-N hydrogen bonds of the 7AI dimer.

  9. Adaptive chemistry of bifunctional gold nanoparticles at the air/water interface. A synchrotron X-ray study of giant amphiphiles

    DEFF Research Database (Denmark)

    Nørgaard, K.; Weygand, M.J.; Kjær, K.

    2004-01-01

    A series of ligand stabilized gold nanoparticles with diameters close to 3 nm were studied as Langmuir monolayers at the air/water interface by synchrotron X-ray diffraction and reflectivity. Alkylthiols with different length and/or terminal functional group (hydrophilic or hydrophobic) were...... of environmental responsiveness, as they adapt to an amphiphilic distribution of ligands around the gold core when spread at the water surface. Likewise nanoparticles of mixed long and short alkyl chains respond to lateral pressure by adopting a structure where the short alkyl chains determine the in-plane nearest...... introduced into the ligand shell by ligand place exchange reactions. Synchrotron grazing incidence X-ray diffraction (GIXD) and specular X-ray reflectivity reveal the well known hexagonally packed monolayers. In addition the mixed hydrophilic/ hydrophobic ligand shell nanoparticles show a high degree...

  10. The roles of counterion and water in a stereoselective cysteine-catalyzed Rauhut-Currier reaction: a challenge for computational chemistry.

    Science.gov (United States)

    Osuna, Sílvia; Dermenci, Alpay; Miller, Scott J; Houk, K N

    2013-10-11

    The stereoselective Rauhut-Currier (RC) reaction catalyzed by a cysteine derivative has been explored computationally with density functional theory (M06-2X). Both methanethiol and a chiral cysteine derivative were studied as nucleophiles. The complete reaction pathway involves rate-determining elimination of the thiol catalyst from the Michael addition product. The stereoselective Rauhut-Currier reaction, catalyzed by a cysteine derivative as a nucleophile, has also been studied in detail. This reaction was experimentally found to be extremely sensitive to the reaction conditions, such as the number of water equivalents and the effect of potassium counterion. The E1cB process for catalyst elimination has been explored computationally for the eight possible stereoisomers. The effect of explicit water solvation and the presence of counterion (either K(+) or Na(+) ) has been studied for the lowest energy enantiomer pair (1S, 2R, 3S)/(1R, 2S, 3R).

  11. Solution chemistry of a water-soluble eta2-H2 ruthenium complex: evidence for coordinated H2 acting as a hydrogen bond donor.

    Science.gov (United States)

    Szymczak, Nathaniel K; Zakharov, Lev N; Tyler, David R

    2006-12-13

    The ability of an eta2-H2 ligand to participate in intermolecular hydrogen bonding in solution has long been an unresolved issue. Such species are proposed to be key intermediates in numerous important reactions such as the proton-transfer pathway of H2 production by hydrogenase enzymes. We present the synthesis of several new water-soluble ruthenium coordination complexes including an eta2-H2 complex that is surprisingly inert to substitution by water. The existence of dihydrogen hydrogen bonding (DHHB) was experimentally probed by monitoring the chemical shift of H-bonded Ru-(H2) complexes using NMR spectroscopy, by UV-visible spectroscopy, and by monitoring the rotational dynamics of a hydrogen-bonding probe molecule. The results provide strong evidence that coordinated H2 can indeed participate in intermolecular hydrogen bonding to bulk solvent and other H-bond acceptors.

  12. Organozinc Chemistry Enabled by Micellar Catalysis. Palladium-Catalyzed Cross-Couplings between Alkyl and Aryl Bromides in Water at Room Temperature.

    Science.gov (United States)

    Duplais, Christophe; Krasovskiy, Arkady; Lipshutz, Bruce H

    2011-11-28

    Negishi-like cross-couplings between (functionalized) alkyl and aryl bromides are described. Despite the fact that organozinc reagents are intolerant of water, their formation as well as their use in an aqueous micellar environment is discussed herein. Each component of this complex series of events leading up to C-C bond formation has an important role which has been determined insofar as the type of zinc, amine ligand, surfactant, and palladium catalyst are concerned. In particular, the nature of the surfactant has been found to be crucial in order to obtain synthetically useful results involving highly reactive, moisture-sensitive organometallics. Neither organic solvent nor heat is required for these cross-couplings to occur; just add water.

  13. Porewater chemistry in compacted bentonite

    Energy Technology Data Exchange (ETDEWEB)

    Muurinen, A.; Lehikoinen, J. [VTT Chemical Technology, Espoo (Finland)

    1999-03-01

    In this study, the porewater chemistry in compacted bentonite, considered as an engineered barrier in the repository of spent fuel, has been studied in interaction experiments. Many parameters, like the composition and density of bentonite, composition of the solution, bentonite-to-water ratio (B/W), surrounding conditions and experimental time have been varied in the experiments. At the end of the interaction the equilibrating solution, the porewaters squeezed out of the bentonite samples, and bentonites themselves were analyzed to give information for the interpretation and modelling of the interaction. Equilibrium modelling was performed with the HYDRAQL/CE computer code 33 refs.

  14. Continuous Chemistry in Ice Cores

    DEFF Research Database (Denmark)

    Kjær, Helle Astrid

    on parameters involved in the study of photolysis as a source of in situ CO2. The concentration of organic substances in Greenland ice is poorly known due to their low levels and the fact that only a few studies evaluate the concentrations of specific organic compounds. Light does not penetrate deep...... depth was found as a function of wavelength. Further, by computational chemistry hybrid density functional methods (DFT), the four most common conformers of pyruvic acid were investigated in both gas, water and ice using the DFT model CAM-B3LYP with dielectric medium methods. A de rease of the energy...

  15. Biosynthetic inorganic chemistry.

    Science.gov (United States)

    Lu, Yi

    2006-08-25

    Inorganic chemistry and biology can benefit greatly from each other. Although synthetic and physical inorganic chemistry have been greatly successful in clarifying the role of metal ions in biological systems, the time may now be right to utilize biological systems to advance coordination chemistry. One such example is the use of small, stable, easy-to-make, and well-characterized proteins as ligands to synthesize novel inorganic compounds. This biosynthetic inorganic chemistry is possible thanks to a number of developments in biology. This review summarizes the progress in the synthesis of close models of complex metalloproteins, followed by a description of recent advances in using the approach for making novel compounds that are unprecedented in either inorganic chemistry or biology. The focus is mainly on synthetic "tricks" learned from biology, as well as novel structures and insights obtained. The advantages and disadvantages of this biosynthetic approach are discussed.

  16. Alcohol combustion chemistry

    KAUST Repository

    Sarathy, Mani

    2014-10-01

    Alternative transportation fuels, preferably from renewable sources, include alcohols with up to five or even more carbon atoms. They are considered promising because they can be derived from biological matter via established and new processes. In addition, many of their physical-chemical properties are compatible with the requirements of modern engines, which make them attractive either as replacements for fossil fuels or as fuel additives. Indeed, alcohol fuels have been used since the early years of automobile production, particularly in Brazil, where ethanol has a long history of use as an automobile fuel. Recently, increasing attention has been paid to the use of non-petroleum-based fuels made from biological sources, including alcohols (predominantly ethanol), as important liquid biofuels. Today, the ethanol fuel that is offered in the market is mainly made from sugar cane or corn. Its production as a first-generation biofuel, especially in North America, has been associated with publicly discussed drawbacks, such as reduction in the food supply, need for fertilization, extensive water usage, and other ecological concerns. More environmentally friendly processes are being considered to produce alcohols from inedible plants or plant parts on wasteland. While biofuel production and its use (especially ethanol and biodiesel) in internal combustion engines have been the focus of several recent reviews, a dedicated overview and summary of research on alcohol combustion chemistry is still lacking. Besides ethanol, many linear and branched members of the alcohol family, from methanol to hexanols, have been studied, with a particular emphasis on butanols. These fuels and their combustion properties, including their ignition, flame propagation, and extinction characteristics, their pyrolysis and oxidation reactions, and their potential to produce pollutant emissions have been intensively investigated in dedicated experiments on the laboratory and the engine scale

  17. Rapid Screening of Carboxylic Acids from Waste and Surface Waters by ESI-MS/MS Using Barium Ion Chemistry and On-Line Membrane Sampling

    Science.gov (United States)

    Duncan, Kyle D.; Volmer, Dietrich A.; Gill, Chris G.; Krogh, Erik T.

    2016-03-01

    Negative ion tandem mass spectrometric analysis of aliphatic carboxylic acids often yields only non-diagnostic ([M - H]-) ions with limited selective fragmentation. However, carboxylates cationized with Ba2+ have demonstrated efficient dissociation in positive ion mode, providing structurally diagnostic product ions. We report the application of barium adducts followed by collision induced dissociation (CID), to improve selectivity for rapid screening of carboxylic acids in complex aqueous samples. The quantitative MS/MS method presented utilizes common product ions of [M - H + Ba]+ precursor ions. The mechanism of product ion formation is investigated using isotopically labeled standards and a series of structurally related carboxylic acids. The results suggest that hydrogen atoms in the β and γ positions yield common product ions ([BaH]+ and [BaOH]+). Furthermore, the diagnostic product ion at m/z 196 serves as a qualifying ion for carboxylate species. This methodology has been successfully used in conjunction with condensed phase membrane introduction mass spectrometry (CP-MIMS), with barium acetate added directly to the methanol acceptor phase. The combination enables rapid screening of carboxylic acids directly from acidified water samples (wastewater effluent, spiked natural waters) using a capillary hollow fiber PDMS membrane immersion probe. We have applied this technique for the direct analysis of complex naphthenic acid mixtures spiked into natural surface waters using CP-MIMS. Selectivity at the ionization and tandem mass spectrometry level eliminate isobaric interferences from hydroxylated species present within the samples, which have been observed in negative electrospray ionization.

  18. Rapid Screening of Carboxylic Acids from Waste and Surface Waters by ESI-MS/MS Using Barium Ion Chemistry and On-Line Membrane Sampling.

    Science.gov (United States)

    Duncan, Kyle D; Volmer, Dietrich A; Gill, Chris G; Krogh, Erik T

    2016-03-01

    Negative ion tandem mass spectrometric analysis of aliphatic carboxylic acids often yields only non-diagnostic ([M - H](-)) ions with limited selective fragmentation. However, carboxylates cationized with Ba(2+) have demonstrated efficient dissociation in positive ion mode, providing structurally diagnostic product ions. We report the application of barium adducts followed by collision induced dissociation (CID), to improve selectivity for rapid screening of carboxylic acids in complex aqueous samples. The quantitative MS/MS method presented utilizes common product ions of [M - H + Ba](+) precursor ions. The mechanism of product ion formation is investigated using isotopically labeled standards and a series of structurally related carboxylic acids. The results suggest that hydrogen atoms in the β and γ positions yield common product ions ([BaH](+) and [BaOH](+)). Furthermore, the diagnostic product ion at m/z 196 serves as a qualifying ion for carboxylate species. This methodology has been successfully used in conjunction with condensed phase membrane introduction mass spectrometry (CP-MIMS), with barium acetate added directly to the methanol acceptor phase. The combination enables rapid screening of carboxylic acids directly from acidified water samples (wastewater effluent, spiked natural waters) using a capillary hollow fiber PDMS membrane immersion probe. We have applied this technique for the direct analysis of complex naphthenic acid mixtures spiked into natural surface waters using CP-MIMS. Selectivity at the ionization and tandem mass spectrometry level eliminate isobaric interferences from hydroxylated species present within the samples, which have been observed in negative electrospray ionization.

  19. Determining alpha-tocopherol distributions between the oil, water, and interfacial regions of macroemulsions: novel applications of electroanalytical chemistry and the pseudophase kinetic model.

    Science.gov (United States)

    Gunaseelan, K; Romsted, Laurence S; Gallego, Maria-Jose Pastoriza; González-Romero, Elisa; Bravo-Díaz, Carlos

    2006-11-16

    The assumptions of the pseudophase model for chemical reactivity in homogeneous microemulsions are used to determine the distribution of alpha-tocopherol (TOC) in macroemulsions from changes in the observed rate constant (k(obs)) for reaction between 4-hexadecylarenediazonium ion (16-ArN2+) probe and TOC with increasing surfactant concentration. Two partition constants are needed to describe the distribution of TOC or other antioxidant (AO) or polar uncharged molecule between the oil and interfacial (P(O)(I)) and the water and interfacial (P(W)(I)) regions of stirred fluid emulsions. The observed rate constants are measured electrochemically. Here we report values of P(O)(I) and P(W)(I) for the distribution of TOC in octane/acidic water/C12E6 (hexaethylene glycol monododecyl ether) and octane/acidic water/C12E4 (Brij 30, tetraethylene glycol dodecyl ether) emulsions obtained by fitting two kinetic data sets with an equation based on the pseudophase model and solving two equations in two unknowns. The partition constants were used to estimate the %TOC in each region of the emulsions. In 1:1 oil:water C12E6 emulsions, at 2% volume fraction of C12E6, 73% of TOC is in the interfacial region, 26% in the octane and about 1% in the water. The distributions of TOC in C12E4 emulsions are similar. The combined electrochemical-pseudophase model approach is applicable to any AO or other compound that reacts with 16-ArN2+. The second-order rate constant, k(I), for reaction in the interfacial region of the emulsions is also estimated from the kinetic data and is about the same for both surfactants (k(I) approximately 0.1-0.2 M(-1)s(-1)) showing that the medium properties of the interfacial regions of C12E6 and C12E4 emulsions are similar. Comparison of these rate constants for a variety of AOs may provide a scale of AO efficiency that is independent of AO distribution between the oil, interfacial and aqueous regions of emulsions.

  20. The 2005 catastrophic acid crater lake drainage, lahar, and acidic aerosol formation at Mount Chiginagak volcano, Alaska, USA: Field observations and preliminary water and vegetation chemistry results

    Science.gov (United States)

    Schaefer, J.R.; Scott, W.E.; Evans, William C.; Jorgenson, J.; McGimsey, R.G.; Wang, B.

    2008-01-01

    A mass of snow and ice 400-m-wide and 105-m-thick began melting in the summit crater of Mount Chiginagak volcano sometime between November 2004 and early May 2005, presumably owing to increased heat flux from the hydrothermal system, or possibly from magma intrusion and degassing. In early May 2005, an estimated 3.8??106 m3 of sulfurous, clay-rich debris and acidic water, with an accompanying acidic aerosol component, exited the crater through a tunnel at the base of a glacier that breaches the south crater rim. Over 27 km downstream, the acidic waters of the flood inundated an important salmon spawning drainage, acidifying Mother Goose Lake from surface to depth (approximately 0.5 km3 in volume at a pH of 2.9 to 3.1), killing all aquatic life, and preventing the annual salmon run. Over 2 months later, crater lake water sampled 8 km downstream of the outlet after considerable dilution from glacial meltwater was a weak sulfuric acid solution (pH = 3.2, SO4 = 504 mg/L, Cl = 53.6 mg/L, and F = 7.92 mg/L). The acid flood waters caused severe vegetation damage, including plant death and leaf kill along the flood path. The crater lake drainage was accompanied by an ambioructic flow of acidic aerosols that followed the flood path, contributing to defoliation and necrotic leaf damage to vegetation in a 29 km2 area along and above affected streams, in areas to heights of over 150 m above stream level. Moss species killed in the event contained high levels of sulfur, indicating extremely elevated atmospheric sulfurcontent. The most abundant airborne phytotoxic constituent was likely sulfuric acid aerosols that were generated during the catastrophic partial crater lake drainage event. Two mechanisms of acidic aerosol formation are proposed: (1) generation of aerosol mist through turbulent flow of acidic water and (2) catastrophic gas exsolution. This previously undocumented phenomenon of simultaneous vegetationdamaging acidic aerosols accompanying drainage of an acidic crater

  1. Bioinorganic Chemistry of the Alkali Metal Ions.

    Science.gov (United States)

    Kim, Youngsam; Nguyen, Thuy-Tien T; Churchill, David G

    2016-01-01

    The common Group 1 alkali metals are indeed ubiquitous on earth, in the oceans and in biological systems. In this introductory chapter, concepts involving aqueous chemistry and aspects of general coordination chemistry and oxygen atom donor chemistry are introduced. Also, there are nuclear isotopes of importance. A general discussion of Group 1 begins from the prevalence of the ions, and from a comparison of their ionic radii and ionization energies. While oxygen and water molecule binding have the most relevance to biology and in forming a detailed understanding between the elements, there is a wide range of basic chemistry that is potentially important, especially with respect to biological chelation and synthetic multi-dentate ligand design. The elements are widely distributed in life forms, in the terrestrial environment and in the oceans. The details about the workings in animal, as well as plant life are presented in this volume. Important biometallic aspects of human health and medicine are introduced as well. Seeing as the elements are widely present in biology, various particular endogenous molecules and enzymatic systems can be studied. Sodium and potassium are by far the most important and central elements for consideration. Aspects of lithium, rubidium, cesium and francium chemistry are also included; they help in making important comparisons related to the coordination chemistry of Na(+) and K(+). Physical methods are also introduced.

  2. Annual Report 1984. Chemistry Department

    DEFF Research Database (Denmark)

    Funck, Jytte; Nielsen, Ole John

    This report contains a brief survey of the main activities in the Chemistry Department. All articles and reports published and lectures given in 1984 are presented. The facilities and equipment are mentioned briefly. The activities are divided into the following groups: radioisotope chemistry, an......, analytical- and organic chemistry, environmental chemistry, polymer chemistry, geochemistry and waste disposal, radical chemistry, positron annihilation, mineral processing, and general.......This report contains a brief survey of the main activities in the Chemistry Department. All articles and reports published and lectures given in 1984 are presented. The facilities and equipment are mentioned briefly. The activities are divided into the following groups: radioisotope chemistry...

  3. Gases (CH4, CO2 and N2 and pore water chemistry in the surface sediments of Lake Orta, Italy: acidification effects on C and N gas cycling

    Directory of Open Access Journals (Sweden)

    Donald D. ADAMS

    2001-02-01

    Full Text Available Lake Orta, a subalpine, warm monomictic lake in northwestern Italy was heavily polluted from rayon factory discharges of ammonium and copper since 1926. In the 1950s accumulations of contaminants resulted in whole lake pHs of 3.8-4.0 from ammonium oxidation. Partial remediation started in the 1950s, but by 1985-89 the water remained acidified at pHs of 4.0. Artificial liming (14,500 t in 1989-90 resulted in improved water quality and substantial recovery of the biological community. Sediment gases, sampled in 1989 before liming, from the lake's four basins showed severe inhibition of methanogenesis (CH4 = 0.0-0.15 mM in the surface sediments (0.5-5 cm of the southern basin, location of the plant effluent, as compared to the deep central and northern basins (0.9-1.4 mM. Four years after liming, cores collected in 1994 near the 1989 southern basin sites showed a slight change in surface sediment methane (0.07-0.82 mM, yet suggested continual sediment toxicity, at least to carbon cycling through methanogenesis. Calculations of diffuse flux of CH4 at the sediment-water interface (SWI in 1989 were 6.6-7.4 mM m-2 day-1 for the central and northern basins and 0.13 for the southern basin. CH4 fluxes increased 16x to 2 mM m-2 day-1 in 1994 in the southern basin, possibly from remediation of near surface sediments. The impact of pollution on denitrification (formation of sediment N2 gas was not so obvious since two processes could counteract each other (high NO3 - stimulating denitrification versus possible negative effects from acidity and metals. The calculated flux of N2 from the southern basin sediments increased 5x four years after liming compared to the period of acidification, suggesting possible toxicity towards denitrifiers during the earlier period. Core overlying water (0.68 mM exhibited N2 concentrations close to saturation, while most surface sediments were twice as much (1.5 mM. Surface (0-6 cm sediment N2 was similar at most sites, with the

  4. Water-Chemistry and On-Site Sulfur-Speciation Data for Selected Springs in Yellowstone National Park, Wyoming, 1996-1998

    Science.gov (United States)

    Ball, James W.; Nordstrom, Kirk D.; McCleskey, R. Blaine; Schoonen, Martin A.A.; Xu, Yong

    2001-01-01

    Fifty-eight water analyses are reported for samples collected from 19 hot springs and their overflow drainages and one ambient-temperature acid stream in Yellowstone National Park (YNP) during 1996-98. These water samples were collected and analyzed as part of research investigations on microbially mediated sulfur oxidation in stream waters and sulfur redox speciation in hot springs in YNP and chemical changes in overflow drainages that affect major ions, redox species, and trace elements. The research on sulfur redox speciation in hot springs is a collaboration with the State University of New York at Stony Brook, Northern Arizona University, and the U.S. Geological Survey (USGS). One ambient-temperature acidic stream system, Alluvium Creek and its tributaries in Brimstone Basin, was studied in detail. Analyses were performed adjacent to the sampling site, in an on-site mobile laboratory truck, or later in a USGS laboratory, depending on stability and preservability of the constituent. Water temperature, specific conductance, pH, Eh, dissolved oxygen (D.O.), and dissolved H2S were determined on-site at the time of sampling. Alkalinity and F were determined within a few days of sample collection by titration and by ion-selective electrode, respectively. Concentrations of S2O3 and SxO6 were determined as soon as possible (minutes to hours later) by ion chromatography (IC). Concentrations of Cl, SO4, and Br were determined by IC within a few days of sample collection. Concentrations of Fe(II) and Fe(total) were determined by ultraviolet/visible spectrophotometry within a few days of sample collection. Densities were determined later in the USGS laboratory. Concentrations of Li, Na, and K were determined by flame atomic absorption (Li) and emission (Na, K) spectrometry. Concentrations of Al, As(total), B, Ba, Be, Ca, Cd, Co, Cr, Cu, Fe(total), Mg, Mn, Ni, Pb, Si, Sr, V, and Zn were determined by inductively-coupled plasma optical emission spectrometry. Trace

  5. Radiation Chemistry Section

    Energy Technology Data Exchange (ETDEWEB)

    None

    1973-12-31

    collaboration with Desalination and Effluent Engineering Division. Preliminary experiments with a valved-out test section in TAPS established the feasibility of achieving chemical decontamination. The initial Water Chemistry in RAPP-1 prior to and after criticality was closely observed and the data were analyzed. Opportunity was also taken during this period to observe the addition and removal of boric acid to the moderator system. In a joint program with the Metallurgy and the Reactor Operations Divisions the hot conditioning of the primary heat transport system of RAPP was followed by chemical and metallurgical evaluation of coupons especially installed for that purpose. In order to keep a close watch on material compatibility, the composition of crud samples from the primary heat transport was evaluated by several techniques. (auth)

  6. Presidential Green Chemistry Challenge: 2011 Designing Greener Chemicals Award

    Science.gov (United States)

    Presidential Green Chemistry Challenge 2011 award winner, Sherwin-Williams, developed water-based acrylic alkyd paints with VOCs that can be made from recycled soda bottle (PET), acrylics, and soybean oil.

  7. Buffer Capacity, Ecosystem Feedbacks, and Seawater Chemistry under Global Change

    Directory of Open Access Journals (Sweden)

    Robert J. Toonen

    2013-09-01

    Full Text Available Ocean acidification (OA results in reduced seawater pH and aragonite saturation state (Ωarag, but also reduced seawater buffer capacity. As buffer capacity decreases, diel variation in seawater chemistry increases. However, a variety of ecosystem feedbacks can modulate changes in both average seawater chemistry and diel seawater chemistry variation. Here we model these effects for a coastal, reef flat ecosystem. We show that an increase in offshore pCO2 and temperature (to 900 µatm and + 3 °C can increase diel pH variation by as much as a factor of 2.5 and can increase diel pCO2 variation by a factor of 4.6, depending on ecosystem feedbacks and seawater residence time. Importantly, these effects are different between day and night. With increasing seawater residence time and increasing feedback intensity, daytime seawater chemistry becomes more similar to present-day conditions while nighttime seawater chemistry becomes less similar to present-day conditions. Recent studies suggest that carbonate chemistry variation itself, independent of the average chemistry conditions, can have important effects on marine organisms and ecosystem processes. Better constraining ecosystem feedbacks under global change will improve projections of coastal water chemistry, but this study shows the importance of considering changes in both average carbonate chemistry and diel chemistry variation for organisms and ecosystems.

  8. Gas phase ion chemistry

    CERN Document Server

    Bowers, Michael T

    1979-01-01

    Gas Phase Ion Chemistry, Volume 1 covers papers on the advances of gas phase ion chemistry. The book discusses the advances in flow tubes and the measurement of ion-molecule rate coefficients and product distributions; the ion chemistry of the earth's atmosphere; and the classical ion-molecule collision theory. The text also describes statistical methods in reaction dynamics; the state selection by photoion-photoelectron coincidence; and the effects of temperature and pressure in the kinetics of ion-molecule reactions. The energy distribution in the unimolecular decomposition of ions, as well

  9. Mathematics for physical chemistry

    CERN Document Server

    Mortimer, Robert G

    2013-01-01

    Mathematics for Physical Chemistry is the ideal supplementary text for practicing chemists and students who want to sharpen their mathematics skills while enrolled in general through physical chemistry courses. This book specifically emphasizes the use of mathematics in the context of physical chemistry, as opposed to being simply a mathematics text. This 4e includes new exercises in each chapter that provide practice in a technique immediately after discussion or example and encourage self-study. The early chapters are constructed around a sequence of mathematical topics, wit

  10. Experiments in physical chemistry

    CERN Document Server

    Wilson, J M; Denaro, A R

    1968-01-01

    Experiments in Physical Chemistry, Second Edition provides a compilation of experiments concerning physical chemistry. This book illustrates the link between the theory and practice of physical chemistry. Organized into three parts, this edition begins with an overview of those experiments that generally have a simple theoretical background. Part II contains experiments that are associated with more advanced theory or more developed techniques, or which require a greater degree of experimental skill. Part III consists of experiments that are in the nature of investigations wherein these invest

  11. Spatially Resolved Artificial Chemistry

    DEFF Research Database (Denmark)

    Fellermann, Harold

    2009-01-01

    Although spatial structures can play a crucial role in chemical systems and can drastically alter the outcome of reactions, the traditional framework of artificial chemistry is a well-stirred tank reactor with no spatial representation in mind. Advanced method development in physical chemistry has...... made a class of models accessible to the realms of artificial chemistry that represent reacting molecules in a coarse-grained fashion in continuous space. This chapter introduces the mathematical models of Brownian dynamics (BD) and dissipative particle dynamics (DPD) for molecular motion and reaction...

  12. Fluorine in medicinal chemistry.

    Science.gov (United States)

    Swallow, Steven

    2015-01-01

    Since its first use in the steroid field in the late 1950s, the use of fluorine in medicinal chemistry has become commonplace, with the small electronegative fluorine atom being a key part of the medicinal chemist's repertoire of substitutions used to modulate all aspects of molecular properties including potency, physical chemistry and pharmacokinetics. This review will highlight the special nature of fluorine, drawing from a survey of marketed fluorinated pharmaceuticals and the medicinal chemistry literature, to illustrate key concepts exploited by medicinal chemists in their attempts to optimize drug molecules. Some of the potential pitfalls in the use of fluorine will also be highlighted.

  13. Characterizing Hydraulic Properties and Ground-Water Chemistry in Fractured-Rock Aquifers: A User's Manual for the Multifunction Bedrock-Aquifer Transportable Testing Tool (BAT3)

    Science.gov (United States)

    Shapiro, Allen M.

    2007-01-01

    A borehole testing apparatus has been designed to isolate discrete intervals of a bedrock borehole and conduct hydraulic tests or collect water samples for geochemical analyses. This borehole testing apparatus, referred to as the Multifunction Bedrock-Aquifer Transportable Testing Tool (BAT3), includes two borehole packers, which when inflated can form a pressure-tight seal against smooth borehole walls; a pump apparatus to withdraw water from between the two packers; a fluid-injection apparatus to inject water between the two packers; pressure transducers to monitor fluid pressure between the two packers, as well as above and below the packers; flowmeters to monitor rates of fluid withdrawal or fluid injection; and data-acquisition equipment to record and store digital records from the pressure transducers and flowmeters. The generic design of this apparatus was originally discussed in United States Patent Number 6,761,062 (Shapiro, 2004). The prototype of the apparatus discussed in this report is designed for boreholes that are approximately 6 inches in diameter and can be used to depths of approximately 300 feet below land surface. The apparatus is designed to fit in five hard plastic boxes that can be shipped by overnight freight car-riers. The equipment can be assembled rapidly once it is removed from the shipping boxes, and the length of the test interval (the distance between the two packers) can be adjusted to account for different borehole conditions without reconfiguring the downhole components. The downhole components of the Multifunction BAT3 can be lowered in a borehole using steel pipe or a cable; a truck mounted winch or a winch and tripod can be used for this purpose. The equipment used to raise and lower the downhole components of the Multifunction BAT3 must be supplied on site, along with electrical power, a compressor or cylinders of compressed gas to inflate the packers and operate downhole valves, and the proper length of tubing to connect the

  14. Characterization of the cell surface and cell wall chemistry of drinking water bacteria by combining XPS, FTIR spectroscopy, modeling, and potentiometric titrations.

    Science.gov (United States)

    Ojeda, Jesús J; Romero-Gonzalez, María E; Bachmann, Robert T; Edyvean, Robert G J; Banwart, Steven A

    2008-04-15

    Aquabacterium commune, a predominant member of European drinking water biofilms, was chosen as a model bacterium to study the role of functional groups on the cell surface that control the changes in the chemical cell surface properties in aqueous electrolyte solutions at different pH values. Cell surface properties of A. commune were examined by potentiometric titrations, modeling, X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared (FTIR) spectroscopy. By combining FTIR data at different pH values and potentiometric titration data with thermodynamic model optimization, the presence, concentration, and changes of organic functional groups on the cell surface (e.g., carboxyl, phosphoryl, and amine groups) were inferred. The pH of zero proton charge, pH(zpc) = 3.7, found from titrations of A. commune at different electrolyte concentrations and resulting from equilibrium speciation calculations suggests that the net surface charge is negative at drinking water pH in the absence of other charge determining ions. In situ FTIR was used to describe and monitor chemical interactions between bacteria and liquid solutions at different pH in real time. XPS analysis was performed to quantify the elemental surface composition, to assess the local chemical environment of carbon and oxygen at the cell wall, and to calculate the overall concentrations of polysaccharides, peptides, and hydrocarbon compounds of the cell surface. Thermodynamic parameters for proton adsorption are compared with parameters for other gram-negative bacteria. This work shows how the combination of potentiometric titrations, modeling, XPS, and FTIR spectroscopy allows a more comprehensive characterization of bacterial cell surfaces and cell wall reactivity as the initial step to understand the fundamental mechanisms involved in bacterial adhesion to solid surfaces and transport in aqueous systems.

  15. Influence of water chemistry and natural organic matter on active and passive uptake of inorganic mercury by gills of rainbow trout (Oncorhynchus mykiss)

    Energy Technology Data Exchange (ETDEWEB)

    Klinck, Joel [Department of Biology, Wilfrid Laurier University, Waterloo, Ont., N2L 3C5 (Canada); Dunbar, Michael [Department of Biology, Wilfrid Laurier University, Waterloo, Ont., N2L 3C5 (Canada); Brown, Stephanie [Department of Biology, Wilfrid Laurier University, Waterloo, Ont., N2L 3C5 (Canada); Nichols, Joel [Department of Biology, Wilfrid Laurier University, Waterloo, Ont., N2L 3C5 (Canada); Winter, Anna [Department of Biology, Wilfrid Laurier University, Waterloo, Ont., N2L 3C5 (Canada); Hughes, Christopher [Department of Biology, Wilfrid Laurier University, Waterloo, Ont., N2L 3C5 (Canada); Playle, Richard C. [Department of Biology, Wilfrid Laurier University, Waterloo, Ont., N2L 3C5 (Canada)]. E-mail: rplayle@wlu.ca

    2005-03-25

    To distinguish physiologically regulated uptake from passive uptake of inorganic Hg in fish, rainbow trout (Oncorhynchus mykiss) were exposed to inorganic Hg (0.5, 1, or 2 {mu}M total Hg) in ion-poor water with various treatments. Addition of ions to the water (mM concentrations of Ca, K, Cl) did not consistently alter Hg accumulation by trout gills, although there was a trend to higher Hg accumulation at higher ion concentrations. The apical Ca channel blockers Verapamil and lanthanum also did not consistently affect Hg accumulation by trout gills. Pre-treatment of trout with the Na channel blocker Phenamil decreased Hg uptake by about half. These results suggest a combination of physiologically regulated and passive uptake of Hg by trout gills. Strong complexing agents of Hg (EDTA, NTA, ethylenediamine, cysteine) decreased Hg-binding by trout gills in a dose-dependent manner. From these data, a conditional equilibrium binding constant for Hg to the gills was estimated as log K {sub Hg-gill} = 18.0, representing very strong binding of Hg to the gills. This value is a first step in creating a biotic ligand model (BLM) for inorganic Hg and fish. Natural organic matter (2-10 mg C/L) also decreased Hg-binding by trout gills, although mM concentrations of Na, K, and Cl interfered with this effect. At low concentrations of these ions, natural organic matter samples isolated from various sources bound Hg to similar degrees, as judged by Hg accumulation by trout gills. A conditional binding constant to natural organic matter (NOM) was estimated as log K {sub Hg-NOM} = 18.0 with about 0.5 {mu}mol binding sites per mg C, representing strong binding of Hg to NOM.

  16. Assessment of surface water chemistry and algale biodiversity in the Bay of Mostaganem and the Cheliff estuary: North-western Algeria

    Directory of Open Access Journals (Sweden)

    Fatima kies

    2015-03-01

    Full Text Available Anthropogenic activities have led to water quality deterioration in many parts of the word, especially in Northwest Algeria. The current work investigated the spatiotemporal variations of water quality in the Cheliff River, samples for physico-chemical were performed at different periods from 2004 to 2007, the results chowed that nitrate (NO3- intake is very high especially in the month of February 2006 (26 mg/l and February 2007 (37 mg/l, nitrite (NO2- values also exceed the standard for samples taken at the estuary (and the sea, ie 0.96 mg/l in the month of February 2006 and 0.98 mg/l in April 2007;the Ammonium (NH4+ contributions are due to the River because the value recorded at the estuary (4.22 in February 2006 ;silicate (SiO2 varies greatly depending on the River flow resulting from soil leaching SOUR to the estuary where we see the maximum values of 20.10 mg/l in the month of February 2007 and 19.1 mg/l in March 2005. The recorded values of elements phosphorus (PO4--- are high and very variable from 0.01 to 1.90 mg/l for the River, 0.01- 0.80 mg/l for the estuary and 0- 0.49 mg/l for the sea. The analyzed biological confirmed a total of 41 phytoplankton speciesand31 macroalgae species. So, Aquatic ecosystems are particulury vulnerable to environmental change and many are, at present, severely degraded.

  17. Chrysophyte cyst-inferred variability of warm season lake water chemistry and climate in northern Poland: training set and downcore reconstruction

    Science.gov (United States)

    Hernández-Almeida, Iván; Grosjean, Martin; Tylmann, Wojciech; Bonk, Alicja

    2014-05-01

    Transfer Functions based on modern training sets are well established and powerful tools in quantitative paleolimnology and environmental/climate reconstructions. Lake sediments are excellent natural archive to reconstruct long-term climate and environmental fluctuations. In this sense, the project 'Climate of northern Poland during the last 1000 years: Constraining the future with the past' (CLIMPOL) aims to develop quantitative climate reconstruction in northern Poland during the last millennium using lake sediments. The Polish training set consists of Chrysophyte cyst (golden brown algae, class Chrysophyceae) sediment trap and surface sediment samples, and data for 19 environmental variables collected from 50 lakes in northern Poland. Canonical correspondence analyses (CCA) revealed that water electric conductivity, total nitrogen, total phosphorous, turbidity, cation and anion compositions (Ca2+, HCO3-) contributed significantly to explaining chrysophytes distribution in the lakes of the training set. A quantitative transfer function was then developed to estimate Ca2+ (log10 transformed) from modern chrysophyte cysts assemblages using weighted-averaging regression (WA) with classical deshrinking. The bootstrapped regression coefficient (R2boot) was 0.68, with a root-mean square error of prediction (RMSEP) of 0.143 (log10 units). The calibration model was applied to a varved sedimentary sequence (AD 1898-2010) from Lake Żabińskie, Masurian Lakeland (NE Poland). Cyst-inferred lake water Ca2+ concentrations were significantly correlated with zonal wind speed (m•s-1) (R=0.50; padjcysts assemblages in Polish lakes respond to hydrochemical factors driven by climate variability.

  18. Chemistry for Kids.

    Science.gov (United States)

    Sato, Sanae; Majoros, Bela

    1988-01-01

    Reports two methods for interesting children in chemistry. Describes a method for producing large soap bubbles and films for study. Examines the use of simple stories to explain common chemical concepts with example given. Lists titles of available stories. (ML)