Activation analysis in water chemistry

International Nuclear Information System (INIS)

Szabo, A.; Toth, A.

1978-01-01

The potential applications of activation analysis in water chemistry are discussed. The principle, unit operations, the radiation sources and measuring instruments of activation analysis are described. The sensitivity of activation analysis is given in tabulated form for some elements of major importance in water chemistry and the elements readily accessible to determination by measurement of the spontaneous gamma radiation are listed. A few papers selected from the recent international professional literature are finally reviewed, in which the authors report on the results obtained by activation analysis applied to water chemistry. (author)

PWR secondary water chemistry guidelines: Revision 3

International Nuclear Information System (INIS)

Lurie, S.; Bucci, G.; Johnson, L.; King, M.; Lamanna, L.; Morgan, E.; Bates, J.; Burns, R.; Eaker, R.; Ward, G.; Linnenbom, V.; Millet, P.; Paine, J.P.; Wood, C.J.; Gatten, T.; Meatheany, D.; Seager, J.; Thompson, R.; Brobst, G.; Connor, W.; Lewis, G.; Shirmer, R.; Gillen, J.; Kerns, M.; Jones, V.; Lappegaard, S.; Sawochka, S.; Smith, F.; Spires, D.; Pagan, S.; Gardner, J.; Polidoroff, T.; Lambert, S.; Dahl, B.; Hundley, F.; Miller, B.; Andersson, P.; Briden, D.; Fellers, B.; Harvey, S.; Polchow, J.; Rootham, M.; Fredrichs, T.; Flint, W.

1993-05-01

An effective, state-of-the art secondary water chemistry control program is essential to maximize the availability and operating life of major PWR components. Furthermore, the costs related to maintaining secondary water chemistry will likely be less than the repair or replacement of steam generators or large turbine rotors, with resulting outages taken into account. The revised PWR secondary water chemistry guidelines in this report represent the latest field and laboratory data on steam generator corrosion phenomena. This document supersedes Interim PWR Secondary Water Chemistry Recommendations for IGA/SCC Control (EPRI report TR-101230) as well as PWR Secondary Water Chemistry Guidelines--Revision 2 (NP-6239)

Extant or Absent: Formation Water in New York State Drinking Water Wells

Science.gov (United States)

Christian, K.; Lautz, L. K.

2013-12-01

The current moratorium on hydraulic fracturing in New York State (NYS) provides an opportunity to collect baseline shallow groundwater quality data pre-hydraulic fracturing, which is essential for determining the natural variability of groundwater chemistry and to evaluate future claims of impaired groundwater quality if hydraulic fracturing occurs in the State. Concerns regarding the future environmental impact of shale gas extraction in NYS include potential shallow groundwater contamination due to migration of methane or formation water from shale gas extraction sites. Treatment, storage and disposal of saline flowback fluids after gas extraction could also be a source of water contamination. In this study, we combine southern NYS shallow groundwater chemistry data from Project Shale-Water Interaction Forensic Tools (SWIFT, n=60), the National Uranium Resource Evaluation program (NURE, n=684), and the USGS 305(b) Ambient Groundwater Quality Monitoring program (USGS, n=89) to examine evidence of formation water mixing with groundwater using the methodology of Warner et al. (2012). Groundwater characterized as low salinity (20 mg/L Cl-). A plot of bromide versus chloride shows high salinity groundwater samples with Br/Cl ratios >0.0001 fall on the mixing line between low salinity groundwater and Appalachian Basin formation water. Based on the observed linear relationship between bromide and chloride, it appears there is up to 1% formation water mixing with shallow groundwater in the region. The presence of formation water in shallow groundwater would indicate the existence of natural migratory pathways between deep formation wells and shallow groundwater aquifers. A plot of sodium versus chloride also illustrates a linear trend for Type D waters (R^2= 0.776), but the relationship is weaker than that for bromide versus chloride (R^2= 0.924). Similar linear relationships are not observed between other ions and chloride, including Mg, Ca, and Sr. If high salinity

Water chemistry guidance in nuclear power plants in Japan

International Nuclear Information System (INIS)

Uchida, Shunsuke; Okada, Hidetoshi; Suzuki, Hiroaki; Naitoh, Masanori

2012-01-01

Water chemistry plays important roles in safe and reliable plant operation which are very critical for future power rate increases as well as aging plant management. Water chemistry control is required to satisfy the need for improved integrity of target materials, and at the same time it must be optimal for all materials and systems in a plant. Optimal water chemistry can be maintained by expert engineers who are knowledgeable about plant water chemistry, who have sufficient experience with plant operation, and whose knowledge is based on fundamental technologies. One of the latest subjects in the field of water chemistry is achieving suitable technical transfers, in which the achievements and experience with plant water chemistry accumulated by experts are successfully transferred to the next generation of engineers. For this purpose, documents on experience with water chemistry are being compiled as the guidance for water chemistry control and water chemistry standards, e.g., standards for chemical analysis procedures and guidance for water chemistry control procedures. This paper introduces the latest activities in Japan in establishing water chemistry guidance involving water chemistry standards, guidance documents and their supporting documents. (orig.)

BWR water chemistry guidelines and PWR primary water chemistry guidelines in Japan – Purpose and technical background

Energy Technology Data Exchange (ETDEWEB)

Kawamura, Hirotaka, E-mail: kawamuh@criepi.denken.or.jp [Central Research Institute of Electric Power Industry (Japan); Hirano, Hideo [Central Research Institute of Electric Power Industry (Japan); Katsumura, Yousuke [University of Tokyo (Japan); Uchida, Shunsuke [Tohoku University (Japan); Mizuno, Takayuki [Mie University (Japan); Kitajima, Hideaki; Tsuzuki, Yasuo [Japan Nuclear Safety Institute (Japan); Terachi, Takumi [Institute of Nuclear Safety System, Inc. (Japan); Nagase, Makoto; Usui, Naoshi [Hitachi-GE Nuclear Energy, Ltd. (Japan); Takagi, Junichi; Urata, Hidehiro [Toshiba Corporation (Japan); Shoda, Yasuhiko; Nishimura, Takao [Mitsubishi Heavy Industry, Ltd. (Japan)

2016-12-01

Highlights: • Framework of BWR/PWR water chemistry Guidelines in Japan are presented. • Guideline necessity, definitions, philosophy and technical background are mentioned. • Some guideline settings for control parameters and recommendations are explaines. • Chemistry strategy is also mentioned. - Abstract: After 40 years of light water reactor (LWR) operations in Japan, the sustainable development of water chemistry technologies has aimed to ensure the highest coolant system component integrity and fuel reliability performance for maintaining LWRs in the world; additionally, it aimed to achieve an excellent dose rate reduction. Although reasonable control and diagnostic parameters are utilized by each boiling water reactor (BWR) and pressurized water reactor (PWR) owner, it is recognized that specific values are not shared among everyone involved. To ensure the reliability of BWR and PWR operation and maintenance, relevant members of the Atomic Energy Society of Japan (AESJ) decided to establish guidelines for water chemistry. The Japanese BWR and PWR water chemistry guidelines provide strategies to improve material and fuel reliability performance as well as to reduce dosing rates. The guidelines also provide reasonable “control values”, “diagnostic values” and “action levels” for multiple parameters, and they stipulate responses when these levels are exceeded. Specifically, “conditioning parameters” are adopted in the Japanese PWR primary water chemistry guidelines. Good practices for operational conditions are also discussed with reference to long-term experience. This paper presents the purpose, technical background and framework of the preliminary water chemistry guidelines for Japanese BWRs and PWRs. It is expected that the guidelines will be helpful as an introduction to achieve safety and reliability during operations.

BWR water chemistry impurity studies

International Nuclear Information System (INIS)

Ljungberg, L.G.; Korhonen, S.; Renstroem, K.; Hofling, C.G.; Rebensdorff, B.

1990-03-01

Laboratory studies were made on the effect of water impurities on environmental cracking in simulated BWR water of stainless steel, low alloy steel and nickel-base alloys. Constant elongation rate tensile (CERT) tests were run in simulated normal water chemistry (NWC), hydrogen water chemistry (HWC), or start-up environment. Sulfate, chloride and copper with chloride added to the water at levels of a fraction of a ppM were found to be extremely deleterious to all kinds of materials except Type 316 NG. Other detrimental impurities were fluoride, silica and some organic acids, although acetic acid was beneficial. Nitrate and carbon dioxide were fairly inoccuous. Corrosion fatigue and constant load tests on compact tension specimens were run in simulated normal BWR water chemistry (NWC) or hydrogen water chemistry (HWC), without impurities or with added sulfate or carbon dioxide. For sensitized Type 304 SS in NWC, 0.1 ppM sulfate increased crack propagation rates in constant load tests by up to a factor of 100, and in fatigue tests up to a factor of 10. Also, cracking in Type 316 nuclear grade SS and Alloy 600 was enhanced, but to a smaller degree. Carbon dioxide was less detrimental than sulfate. 3 figs., 4 tabs

Water chemistry experiences with VVERs at Kudankulam

International Nuclear Information System (INIS)

Rout, D.; Upadhyaya, T.C.; Ravindranath; Selvinayagam, P.; Sundar, R.S.

2015-01-01

Kudankulam Nuclear Power Project - 1 and 2 (Kudankulam NPP - 1 and 2) are pressurised water cooled VVERs of 1000 MWe each. Kudankulam NPP Unit - 1 is presently on its first cycle of operation and Kudankulam NPP Unit - 2 is on the advanced stage of commissioning with the successful completion of hot run related Functional tests. Water Chemistry aspects during various phases of commissioning of Kudankulam NPP Unit - 1 such as Hot Run, Boric acid flushing, initial fuel Loading (IFL), First approach to Criticality (FAC) are discussed. The main objectives of the use of controlled primary water chemistry programme during the hot functional tests are reviewed. The importance of the relevant water chemistry parameters were ensured to have the quality of the passive layer formed on the primary coolant system surfaces. The operational experiences during the 1 st cycle of operation of primary water chemistry, radioactivity transport and build-up are presented. The operational experience of some VVER units in the field of the primary water chemistry, radioactivity transport and build-up are presented as a comparison to VVER at Kudankulam NPP. The effects of the initial passivated layer formed on metal surfaces during hot run, activated corrosion products levels in the primary coolant under controlled water chemistry regime and the contamination/radiation situation are discussed. This report also includes the water chemistry related issues of secondary water systems. (author)

PWR secondary water chemistry diagnostic system

International Nuclear Information System (INIS)

Miyazaki, S.; Hattori, T.; Yamauchi, S.; Kato, A.; Suganuma, S.; Yoshikawa, T.

1989-01-01

Water chemistry control is one of the most important tasks in order to maintain the reliability of plant equipments and extend operating life of the plant. We developed an advanced water chemistry management system which is able to monitor and diagnose secondary water chemistry. A prototype system had been installed at one plant in Japan since Nov. 1986 in order to evaluate system performance and man-machine interface. The diagnosis system has been successfully tested off line using synthesized plant data for various cases. We are continuing to improve the applicability and develop new technology which make it evaluate steam generator crevice chemistry. (author)

Understanding the acquisition and regulation mechanisms of the water chemistry in a clay formation: the CEC/ANDRA Archimede-argile project

International Nuclear Information System (INIS)

Merceron, T.; Mossmann, J.R.; Neerdael, B.; Canniere, P. de; Beaucaire, C.; Toulhoat, P.; Daumas, S.; Bianchi, A.; Christen, R.

1993-01-01

Clay formations are candidate host environments to high level radioactive waste repository. The radioelements could be partially released from the waste into the host geological formation after a very long time. Understanding behaviour of the natural chemical species is considered as a fundamental prerequisite before the disturbed system will be studied. Additional laboratory studies are also essential in order to forecast, by analogy, the behaviour of radioelements released from the radioactive waste repository. The ARCHIMEDE-ARGILE project has two main goals. The first is to gain an understanding of the mechanisms of acquisition and regulation of the water chemistry in a clay environment. This step is essential to predict both the behaviour and the migration in solution of artificial elements which are initially absent in the clay formation. The second is to test and validate in clay the measured physico chemical parameters which are the basis for the geochemical modelling of the behaviour of the natural and artificial radioelements. The paper presents the main results previously obtained on granitic waters and the research strategy established for the ARCHIMEDE project. (authors). 2 figs., 2 refs

Water chemistry guidelines for BWRs

International Nuclear Information System (INIS)

Bilanin, W.J.; Jones, R.L.; Welty, C.S.

1984-01-01

Guidelines for BWR water chemistry control have been prepared by a committee of experienced utility industry personnel sponsored by the BWR Owners Group on IGSCC Research and coordinated by the Electric Power Research Institute. The guidelines are based on extensive plant operational experience and laboratory research data. The purpose of the guidelines is to provide guidance to the electric utility industry on water chemistry control to help reduce corrosion, especially stress corrosion cracking, in boiling water reactors

EPRI BWR Water Chemistry Guidelines Revision

International Nuclear Information System (INIS)

Garcia, Susan E.; Giannelli, Joseph F.

2014-01-01

BWRVIP-190: BWR Water Chemistry Guidelines – 2008 Revision has been revised. The revision committee consisted of U.S. and non-U.S. utilities (members of the BWR Vessel and Internals Protection (BWRVIP) Mitigation Committee), reactor system manufacturers, fuel suppliers, and EPRI and industry experts. The revised document, BWRVIP-190 Revision 1, was completely reformatted into two volumes, with a simplified presentation of water chemistry control, diagnostic and good practice parameters in Volume 1 and the technical bases in Volume 2, to facilitate use. The revision was developed in parallel and in coordination with preparation of the Fuel Reliability Guidelines Revision 1: BWR Fuel Cladding Crud and Corrosion. Guidance is included for plants operating under normal water chemistry (NWC), moderate hydrogen water chemistry (HWC-M), and noble metal application (GE-Hitachi NobleChem™) plus hydrogen injection. Volume 1 includes significant changes to BWR feedwater and reactor water chemistry control parameters to provide increased assurance of intergranular stress corrosion cracking (IGSCC) mitigation of reactor materials and fuel reliability during all plant conditions, including cold shutdown (≤200°F (93°C)), startup/hot standby (>200°F (93°C) and ≤ 10%) and power operation (>10% power). Action Level values for chloride and sulfate have been tightened to minimize environmentally assisted cracking (EAC) of all wetted surfaces, including those not protected by hydrogen injection, with or without noble metals. Chemistry control guidance has been enhanced to minimize shutdown radiation fields by clarifying targets for depleted zinc oxide (DZO) injection while meeting requirements for fuel reliability. Improved tabular presentations of parameter values explicitly indicate levels at which actions are to be taken and required sampling frequencies. Volume 2 provides the technical bases for BWR water chemistry control for control of EAC, flow accelerated corrosion

Condensate and feedwater systems, pumps, and water chemistry. Volume seven

International Nuclear Information System (INIS)

Anon.

1986-01-01

Subject matter includes condensate and feedwater systems (general features of condensate and feedwater systems, condenser hotwell level control, condensate flow, feedwater flow), pumps (principles of fluid flow, types of pumps, centrifugal pumps, positive displacement pumps, jet pumps, pump operating characteristics) and water chemistry (water chemistry fundamentals, corrosion, scaling, radiochemistry, water chemistry control processes, water pretreatment, PWR water chemistry, BWR water chemistry, condenser circulating water chemistry

Water chemistry in boiling water reactors - A Leibstadt-specific overview

International Nuclear Information System (INIS)

Sarott, F.-A.

2005-01-01

The boiling water reactor (BWR) consists of two main water circuits: the water-steam cycle and the main cooling water system. In the introduction, the goals and tasks of the BWR plant chemistry are described. The most important objectives are the prevention of system degradation by corrosion and the minimisation of radiation fields. Then a short description of the BWR operation principle, including the water steam cycle, the transport of various impurities by the steam, removing impurities from the condensate, the reactor water clean-up system, the balance of plant and the main cooling water system, is given. Subsequently, the focus is set on the water-steam cycle chemistry. In order to fulfil the somewhat contradictory requirements, the chemical parameters must be well balanced. This is achieved by the water chemistry control method called 'normal water chemistry'. Other additional methods are used for the solution to different problems. The 'zinc addition method' is applied to reduce high radiation levels around the recirculation loops. The 'hydrogen water chemistry method' and the 'noble metal chemical addition method' are used to protect the reactor core components and piping made of stainless steel against stress corrosion cracking. This phenomenon has been observed for about 40 years and is partly due to the strong oxidising conditions in the BWR water. Both mitigation methods are used by the majority of the BWR plants all over the world (including the two Swiss NPPs Muehleberg and Leibstadt). (author)

Developments in nuclear power plant water chemistry

International Nuclear Information System (INIS)

Fruzetti, K.; Wood, C.J.

2007-01-01

This paper illustrates the changing role of water chemistry in current operation of nuclear power plants. Water chemistry was sometimes perceived as the cause of materials problems, such as denting in PWR steam generators and intergranular stress corrosion cracking in BWRs. However, starting in the last decade, new chemistry options have been introduced to mitigate stress corrosion cracking and reduce fuel performance concerns. In BWRs and PWRs alike, water chemistry has evolved to successfully mitigate many problems as they have developed. The increasing complexity of the chemistry alternatives, coupled with the pressures to increase output and reduce costs, have demonstrated the need for new approaches to managing plant chemistry, which are addressed in the final part of this paper. (orig.)

Water states and types of water in materials from different argillaceous formations

International Nuclear Information System (INIS)

Fernandez, A.M.; Melon, A.

2010-01-01

Document available in extended abstract form only. Depending of their structure and degree of compaction, clays can be hydrated by a variable amount of water molecules in the inter-lamellar space and on external surfaces. Due to the fact that the structure and nature of water molecules (properties of liquid water) is influenced by the clay surfaces; different types of waters are involved in clayey systems (internal/external water, adsorbed/free water) giving a double porosity structure. The water volume accessible to ions is a key parameter in order to determine the pore water chemistry affecting the radionuclide transport in clay-rocks. In the case of argillaceous formations, natural consolidation induces significant physical and structural changes to clays as a function of time, leading to a progressive compaction and agglomeration of particles, reduction of crystallinity and an increase of micro-strain, which affects both the tetrahedral and octahedral layers. Structure and dynamics of water are modified when water molecules are close to interfaces or confined in porous spaces. At high degrees of compaction, the diffusive transport of the solvated ions and the solvent molecules in clays is substantially retarded compared with the free electrolyte solution because of the surface complexation of ions and the strong ordering of solvent molecules at the solid-liquid interface. Besides, mud-rocks contain a variable amount of different types of clays, such as illite, kaolinite, chlorites, smectite and illite/smectite mixed layers; as well as other main and accessory minerals which influence also the amount of water adsorbed and types of waters in these systems. Structural and dynamic properties of water confined among basal planes of clays have been extensively studied by means of water adsorption isotherms, neutron scattering, molecular dynamics (MD) and Monte- Carlo simulations. However, most of the works are related to purified clays and dispersed systems. In real

Chemistry in water reactors

International Nuclear Information System (INIS)

Hermansson, H.P.; Norring, K.

1994-01-01

The international conference Chemistry in Water Reactors was arranged in Nice 24-27/04/1994 by the French Nuclear Energy Society. Examples of technical program areas were primary chemistry, operational experience, fundamental studies and new technology. Furthermore there were sessions about radiation field build-up, hydrogen chemistry, electro-chemistry, condensate polishing, decontamination and chemical cleaning. The conference gave the impression that there are some areas that are going to be more important than others during the next few years to come. Cladding integrity: Professor Ishigure from Japan emphasized that cladding integrity is a subject of great concern, especially with respect to waterside corrosion, deposition and release of crud. Chemistry control: The control of the iron/nickel concentration quotient seems to be not as important as previously considered. The future operation of a nuclear power plant is going to require a better control of the water chemistry than achievable today. One example of this is solubility control via regulation in BWR. Trends in USA: means an increasing use of hydrogen, minimization of SCC/IASCC, minimization of radiation fields by thorough chemistry control, guarding fuel integrity by minimization of cladding corrosion and minimization of flow assisted corrosion. Stellite replacement: The search for replacement materials will continue. Secondary side crevice chemistry: Modeling and practical studies are required to increase knowledge about the crevice chemistry and how it develops under plant operation conditions. Inhibitors: Inhibitors for IGSCC and IGA as well for the primary- (zinc) as for the secondary side (Ti) should be studied. The effects and mode of operation of the inhibitors should be documented. Chemical cleaning: of heat transfer surfaces will be an important subject. Prophylactic cleaning at regular intervals could be one mode of operation

Advances in water chemistry control for BWRs and PWRs

International Nuclear Information System (INIS)

Wood, C.J.

1997-01-01

This paper is an overview of the effects of water chemistry developments on the current operation of nuclear power plants in the United States, and the mitigation of corrosion-related degradation processes and radiation field build-up processes through the use of advanced water chemistry. Recent modifications in water chemistry to control and reduce radiation fields are outlined, including revisions to the EPRI water chemistry guidelines for BWRs and PWR primary and secondary systems. The change from a single water chemistry specification for all plants to a set of options, from which a plant-specific chemistry programme can be defined, is described. (author)

EPRI PWR primary water chemistry guidelines revision

International Nuclear Information System (INIS)

McElrath, Joel; Fruzzetti, Keith

2014-01-01

EPRI periodically updates the PWR Primary Water Chemistry Guidelines as new information becomes available and as required by NEI 97-06 (Steam Generator Program Guidelines) and NEI 03-08 (Guideline for the Management of Materials Issues). The last revision of the PWR water chemistry guidelines identified an optimum primary water chemistry program based on then-current understanding of research and field information. This new revision provides further details with regard to primary water stress corrosion cracking (PWSCC), fuel integrity, and shutdown dose rates. A committee of industry experts, including utility specialists, nuclear steam supply system (NSSS) and fuel vendor representatives, Institute of Nuclear Power Operations (INPO) representatives, consultants, and EPRI staff collaborated in reviewing the available data on primary water chemistry, reactor water coolant system materials issues, fuel integrity and performance issues, and radiation dose rate issues. From the data, the committee updated the water chemistry guidelines that all PWR nuclear plants should adopt. The committee revised guidance with regard to optimization to reflect industry experience gained since the publication of Revision 6. Among the changes, the technical information regarding the impact of zinc injection on PWSCC initiation and dose rate reduction has been updated to reflect the current level of knowledge within the industry. Similarly, industry experience with elevated lithium concentrations with regard to fuel performance and radiation dose rates has been updated to reflect data collected to date. Recognizing that each nuclear plant owner has a unique set of design, operating, and corporate concerns, the guidelines committee has retained a method for plant-specific optimization. Revision 7 of the Pressurized Water Reactor Primary Water Chemistry Guidelines provides guidance for PWR primary systems of all manufacture and design. The guidelines continue to emphasize plant

Water chemistry control at FBTR

International Nuclear Information System (INIS)

Panigrahi, B.S.; Jambunathan, D.; Suresh Kumar, K.V.; Ramanathan, V.; Srinivasan, G.; Ramalingam, P.V.

2008-01-01

Condenser cooling and service water systems together serve as the cooling water system of Fast Breeder Test Reactor (FBTR). Palar river water serves as the make-up to the cooling water system. Initially, the service water system alone was commissioned in phases depending upon the arrival of auxiliary equipments at site. During this period, the water was not treated chemically and it also inadvertently remained stagnant for some time in some systems. Thereafter, a threshold chemical treatment was started. However, pin-hole leaks and reduced flow through the heat exchangers were observed and therefore chemical cleaning of headers was done and small diameter pipelines were replaced. Following this a full fledged chemistry control with proprietary formulations was initiated. Later the condenser cooling system was commissioned and the chemical treatment was reviewed. With adoption of improved monitoring methodology and treatment formulation satisfactory corrosion control (< 3 mpy) with minimum deposition problem in this system could be achieved. The primary coolant (primary sodium) of FBTR transfers the nuclear heat to the secondary coolant (secondary sodium) that in turn transfers heat to water in Once Through Steam Generator (OTSG) to generate superheated steam (480 deg C at 125 bar). Efficient water chemistry control plays the vital role in minimizing corrosion related failures of steam generator tubes and ensuring steam generator tube integrity. Therefore, the technical specifications of chemistry parameters of feed/steam water at FBTR are made very stringent to maintain the purity of water at the best attainable level. To meet this stringent feed water and steam quality specifications, online monitoring techniques have been employed in the steam/water circuit to get continuous information about the purity. These monitors have helped significantly in achieving the required feed water quality and running the steam generator for more than 25000 hours without any tube

A review of boiling water reactor water chemistry: Science, technology, and performance

International Nuclear Information System (INIS)

Fox, M.J.

1989-02-01

Boiling water reactor (BWR) water chemistry (science, technology, and performance) has been reviewed with an emphasis on the relationships between BWR water quality and corrosion fuel performance, and radiation buildup. A comparison of Nuclear Regulatory Commission (NRC) Regulatory Guide 1.56, the Boiling Water Reactor Owners Group (BWROG) Water Chemistry Guidelines, and Plant Technical Specifications showed that the BWROG Guidelines are more stringent than the NRC Regulatory Guide, which is almost identical to Plant Technical Specifications. Plant performance with respect to BWR water chemistry has shown dramatic improvements in recent years. Up until 1979 BWRs experienced an average of 3.0 water chemistry incidents per reactor-year. Since 1979 the water chemistry technical specifications have been violated an average of only 0.2 times per reactor-year, with the most recent data from 1986-1987 showing only 0.05 violations per reactor-year. The data clearly demonstrate the industry-wide commitment to improving water quality in BWRs. In addition to improving water quality, domestic BWRs are beginning to switch to hydrogen water chemistry (HWC), a remedy for intergranular stress corrosion cracking. Three domestic BWRs are presently operating on HWC, and fourteen more have either performed HWC mini tests or are in various stages of HWC implementation. This report includes a detailed review of HWC science and technology as well as areas in which further research on BWR chemistry may be needed. 43 refs., 30 figs., 8 tabs

Advances in high temperature water chemistry and future issues

International Nuclear Information System (INIS)

Millett, P.J.

2005-01-01

This paper traces the development of advances in high temperature water chemistry with emphasis in the field of nuclear power. Many of the water chemistry technologies used in plants throughout the world today would not have been possible without the underlying scientific advances made in this field. In recent years, optimization of water chemistry has been accomplished by the availability of high temperature water chemistry codes such as MULTEQ. These tools have made the science of high temperature chemistry readily accessible for engineering purposes. The paper closes with a discussion of what additional scientific data and insights must be pursued in order to support the further development of water chemistry technologies for the nuclear industry. (orig.)

The water chemistry of CANDU PHW reactors

International Nuclear Information System (INIS)

LeSurf, J.E.

1978-01-01

This review will discuss the chemistry of the three major water circuits in a CANDU-PHW reactor, viz., the Primary Heat Transport (PHT) water, the moderator and the boiler water. An important consideration for the PHT chemistry is the control of corrosion and of the transport of corrosion products to minimize the growth of radiation fields. In new reactors the PHT will be allowed to boil, requiring reconsideration of the methods used to radiolytic oxygen and elevate the pH. Separation of the moderator from the PHT in the pressure-tubed CANDU design permits better optimization of the chemistry of each system, avoiding the compromises necessary when the same water serves both functions. Major objectives in moderator chemistry are to control (a) the radiolytic decomposition of D 2 0; (b) the concentration of soluble neutron poisons added to adjust reactivity; and (c) the chemistry of shutdown systems. The boiler water and its feed water are treated to avoid boiler tube corrosion, both during normal operation and when perturbations are caused to the feed by, for example, leaks in the condenser tubes which permit ingress of untreated condenser cooling water. Development of a system for automatic analysis and control of feed water to give rapid, reliable response to abnormal conditions is a novel feature which has been developed for incorporation in future CANDU-PHW reactors. (author)

Water chemistry control to meet the advanced design and operation of light water reactors

International Nuclear Information System (INIS)

Shirai, Hiroshi; Uchida, Shunsuke; Naitoh, Masanori; Okada, Hidetoshi; Sato, Masatoshi

2014-01-01

Water chemistry control is one of the key technologies to establish safe and reliable operation of nuclear power plants. The road maps on R and D plans for water chemistry of nuclear power systems in Japan have been proposed along with promotion of R and D related water chemistry improvement for the advanced application of light water reactors (LWRs). The technical trends were divided into four categories, dose rate reduction, structural integrity, fuel integrity and radioactive waste reduction, and latest technical break through for each category was shown for the advanced application of LWRs. At the same time, the technical break through and the latest movements for regulation of water chemistry were introduced for each of major organizations related to nuclear engineering in the world. The conclusions were summarized as follows; 1. Water chemistry improvements might contribute to achieve the advanced application of LWRs, while water chemistry should be often changed to achieve the advanced application of LWRs. 2. Only one solution for water chemistry control was not obtained for achieving the advanced application of LWRs, but miscellaneous solutions were possible for achieving one. Optimal water chemistry control was desired for having the good practices for satisfying multi-targets at the same time and it was much affected by the plant unique systems and operational history. 3. That meant it was difficult to determine water chemistry regulation targets for achieving application of LWRs but it was necessary to prepare suitable guideline for good achievement of application of LWRs. That meant the guideline should be recommendation for good practice in the plant. 4. The water chemistry guide line should be modified along with progress of plant operation and water chemistry and related technologies. (author)

Optimization of secondary side water chemistry in TQNPC

International Nuclear Information System (INIS)

Fang Lan

2007-01-01

This article briefly introduces the types of corrosion that may be happened on steam generator heat exchange tubes in Qinshan CANDU6 nuclear power station and chemical effects on corrosion. The water chemistry optimization on minimzing deposition and corrosion of steam generators are introduced. The article summarizes the experiences of plant chemistry control and morpholine operation, providing guidance for optimizing secondary side water chemistry in the future, giving reference on selection of secondary side alkali agent and setting water chemistry specifications for other nuclear power stations. (authors)

Survey of Water Chemistry and Corrosion of NPP

Energy Technology Data Exchange (ETDEWEB)

Jung, Ki Sok; Hong, Bong Geon

2008-06-15

Status of water chemistry of nuclear power plant and materials corrosion has been surveyed. For PWR, system chemistry of primary coolant and secondary coolant as well as the related corrosion of materials was surveyed. For BWR, system chemistry as whole has been surveyed with its accompanying corrosion problems. Radiolysis of coolant water and activation of corrosion products also was surveyed. Future NPP such as supercritical water cooled reactor and fusion reactor has also been surveyed for their water chemistry and corrosion problems. As a result, proposal for some research items has been suggested. Some related corrosion research techniques and electrochemical fundamentals are also presented.

Survey of Water Chemistry and Corrosion of NPP

International Nuclear Information System (INIS)

Jung, Ki Sok; Hong, Bong Geon

2008-06-01

Status of water chemistry of nuclear power plant and materials corrosion has been surveyed. For PWR, system chemistry of primary coolant and secondary coolant as well as the related corrosion of materials was surveyed. For BWR, system chemistry as whole has been surveyed with its accompanying corrosion problems. Radiolysis of coolant water and activation of corrosion products also was surveyed. Future NPP such as supercritical water cooled reactor and fusion reactor has also been surveyed for their water chemistry and corrosion problems. As a result, proposal for some research items has been suggested. Some related corrosion research techniques and electrochemical fundamentals are also presented

Water chemistry and corrosion control of cladding and primary circuit components. Proceedings of a technical committee meeting

International Nuclear Information System (INIS)

1999-12-01

Corrosion is the principal life limiting degradation mechanism in nuclear steam supply systems, especially taking into account the trends to increase fuel burnup, thermal rate and cycle length. Primary circuit components of water cooled power reactors have an impact on Zr-based alloys behaviour due to crud (primary circuit corrosion products) formation, transport and deposition on heat transfer surfaces. Crud deposits influence water chemistry, radiation and thermal hydraulic conditions near cladding surface, and by this way-Zr-based alloy corrosion. During the last decade, significant improvements were achieved in the reduction of the corrosion and dose rates by changing the cladding material for one more resistant to corrosion or by the improvement of water chemistry conditions. However, taking into account the above mentioned tendency for heavier fuel duties, corrosion and water chemistry, control will remain a serious task to work with for nuclear power plant operators and scientists, as well as development of generally accepted corrosion model of Zr-based alloys in a water environment in a new millennium. Upon the recommendation of the International Working Group on Water Reactor Fuel Performance and Technology, water chemistry and corrosion of cladding and primary circuit components are in the focus of the IAEA activities in the area of fuel technology and performance. At present the IAEA performs two co-ordinated research projects (CRPs): on On-line High Temperature Monitoring of Water Chemistry and Corrosion (WACOL) and on Activity Transport in Primary Circuits. Two CRPs deal with hydrogen and hydride degradation of the Zr-based alloys. A state-of-the-art review entitled: 'Waterside Corrosion of Zirconium Alloys in Nuclear Power Plants' was published in 1998. Technical Committee meetings on the subject were held in 1985 (Cadarache, France), 1989 (Portland, USA), 1993 (Rez, Czech Republic). During the last few years extensive exchange of experience in

Chemistry and Star Formation: A Love-Hate Relationship

Science.gov (United States)

Jiménez-Serra, Izaskun; Zhang, Qizhou; Patel, Nimesh; Lu, Xing; Wang, Ke; Testi, Leonardo; Caselli, Paola; Martin-Pintado, Jesus

2014-06-01

The development of the broad bandwidth receivers at the Submillimeter Array (SMA) a decade ago opened up the possibility to observe tens of molecular lines at high angular resolution simultaneously. The unprecedented wealth of molecular line data provided by the SMA allowed for the first time detailed studies of the chemistry in star-forming regions. These studies have revealed that chemistry is a useful tool to pin down the internal physical structure and the physical processes involved in the process of low-mass and high-mass star formation. In this talk, I will review the most important advances in our understanding of the star-formation process through chemistry thanks to the SMA, and I will present the challenges that will be faced in the next decade in this field of research thanks to the advent of new instrumentation such as the Atacama Large Millimeter/Submillimeter Array and the Square Kilometer Array.

Combustion chemistry and formation of pollutants; Chimie de la combustion et formation des polluants

Energy Technology Data Exchange (ETDEWEB)

NONE

1996-12-31

This book of proceedings reports on 7 papers on combustion chemistry and formation of pollutants presented during the workshop organized by the `Combustion and Flames` section of the French society of thermal engineers. The chemistry of combustion is analyzed in various situations such as: turbojet engines, spark ignition engines, industrial burners, gas turbines etc... Numerical simulation is used to understand the physico-chemical processes involved in combustion, to describe the kinetics of oxidation, combustion and flame propagation, and to predict the formation of pollutants. (J.S.)

Development of Database and Lecture Book for Nuclear Water Chemistry

International Nuclear Information System (INIS)

Maeng, Wan Young; Kim, U. C.; Na, J. W.; Choi, B. S.; Lee, E. H.; Kim, K. H.; Kim, K. M.; Kim, S. H.; Im, K. S.

2010-02-01

In order to establish a systematic and synthetic knowledge system of nuclear water chemistry, we held nuclear water chemistry experts group meetings. We discussed the way of buildup and propagation of nuclear water chemistry knowledge with domestic experts. We obtained a lot of various opinions that made the good use of this research project. The results will be applied to continuous buildup of domestic nuclear water chemistry knowledge database. Lessons in water chemistry of nuclear power plants (NPPs) have been opened in Nuclear Training and education Center, KAERI to educate the new generation who are working and will be working at the department of water chemistry of NPPs. The lessons were 17 and lesson period was from 12th May through 5th November. In order to progress the programs, many water chemistry experts were invited. They gave lectures to the younger generation once a week for 2 h about their experiences obtained during working on water chemistry of NPPs. The number of attendance was 290. The lessons were very effective and the lesson data will be used to make database for continuous use

Green rust formation controls nutrient availability in a ferruginous water column

DEFF Research Database (Denmark)

Zegeye, Asfaw; Bonneville, Steeve; Benning, Liane G.

2013-01-01

a mechanism for reconstructing ancient ocean chemistry. Such reconstructions depend, however, on precise knowledge of the iron minerals formed in the water column. Here, we combine mineralogical and geochemical analyses to demonstrate formation of the mixed-valence iron mineral, green rust, in ferruginous...

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

Current status of regulatory aspects relating to water chemistry in Japanese NPPs

International Nuclear Information System (INIS)

Sato, Masatoshi

2014-01-01

In nuclear power plants, water chemistry of cooling water is carefully monitored and controlled to keep integrity of structures, systems and components, and to reduce occupational radiation exposures. As increasing demand for advanced application of light water cooled reactors, water chemistry control plays more important roles on plant reliability. The road maps on R and D for water chemistry of nuclear power systems have been proposed along with promotion of R and D related water chemistry in Japan. In academic and engineering societies, non-governmental standards for water chemistry are going to be established. In the present paper, recent trends of water chemistry in Japan have been surveyed. The effects of water chemistry on plant safety and radiation exposures have been discussed. In addition, possible contributions of regulation regarding water chemistry control have been confirmed. Major water chemistry regulatory aspects relating to reactor safety and radiation safety are also outlined in this paper. (author)

Water Chemistry Section: progress report (1981-82)

International Nuclear Information System (INIS)

Dharwadkar, S.R.; Ramshesh, V.

1983-01-01

The activities of the Water Chemistry Section of the Bhabha Atomic Research Centre (BARC), Bombay, during the years 1981 and 1982 are reported in the form of individual summaries. The research activities of the Section cover the following areas: (1) chemistry and thermodynamics of nuclear materials, (2) crystal structure of organo-metallic complexes using X-ray diffraction, (3) thermophysical and phase transition studies, (4) solid state chemistry and thermochemical studies, (5) water and steam chemistry of heavy water plants and phwr type reactors, and (6) uranium isotope exchange studies. A survey is also given of: (i) the Section's participation in advisory and consultancy services in nuclear and thermal power stations, (ii) training activities, and (iii) assistance in chemical analysis by various techniques to other units of BARC and outside agencies. A list of publications and lectures by the staff during the report period is included. (M.G.B.)

Water chemistry and materials degradation in LWR'S

International Nuclear Information System (INIS)

Haenninen, H.; Toerroenen, K.; Aaltonen, P.

1994-01-01

Water chemistry plays a major role in corrosion, in erosion corrosion and in activity transport in NPPs; it impacts upon the operational safety of LWRs in two main ways: integrity of pressure boundary materials and activity transport and out-of-core radiation fields. A good control of water chemistry can significantly reduce these problems and improve plant safety, but economic pressures are leading to more rigorous operating conditions: fuel burnups are to be increased, higher efficiencies are to be achieved by running at higher temperatures and plant lifetimes are to be extended. Typical water chemistry specifications used in PWR and BWR plants are presented and the chemistry optimization is discussed. The complex interplay of metallurgical, mechanical and environmental factors in environmental sensitive cracking is shown, with details on studies for carbon steels, stainless steels and nickel base alloys. 20 refs., 8 figs., 4 tabs

Closed cooling water chemistry guidelines revision

International Nuclear Information System (INIS)

McElrath, Joel; Breckenridge, Richard

2014-01-01

This second revision of the Closed Cooling Water Chemistry Guideline addresses the use of chemicals and monitoring methods to mitigate corrosion, fouling, and microbiological growth in the closed cooling-water (CCW) systems of nuclear and fossil-fueled power plants. This revision has been endorsed by the utility chemistry community and represents another step in developing a more proactive chemistry program to limit or control closed cooling system degradation with increased consideration of corporate resources and plant-specific design and operating concerns. These guidelines were developed using laboratory data, operating experience, and input from organizations and utilities within and outside of the United States of America. It is the intent of the Revision Committee that these guidelines are applicable to all nuclear and fossil-fueled generating stations around the world. A committee of industry experts—including utility specialists, Institute of Nuclear Power Operations representatives, water-treatment service-company representatives, consultants, a primary contractor, and EPRI staff—collaborated in reviewing available data on closed cooling-water system corrosion and microbiological issues. Recognizing that each plant owner has a unique set of design, operating, and corporate concerns, the Guidelines Committee developed a methodology for plant-specific optimization. The guideline provides the technical basis for a reasonable but conservative set of chemical treatment and monitoring programs. The use of operating ranges for the various treatment chemicals discussed in this guideline will allow a power plant to limit corrosion, fouling, and microbiological growth in CCW systems to acceptable levels. The guideline now includes closed cooling chemistry regimes proven successful in use in the international community. The guideline provides chemistry constraints for the use of phosphates control, as well as pure water with pH control. (author)

An Investigation into Water Chemistry in Primary Coolant Circuit of an Advanced Boiling Water Reactor

International Nuclear Information System (INIS)

Wu, Bing-Jhen; Yeh, Tsung-Kuang; Wang, Mei-Ya; Sheu, Rong-Jiun

2012-09-01

To ensure operation safety, an optimization on the coolant chemistry in the primary coolant circuit of a nuclear reactor is essential no matter what type or generation the reactor belongs to. For a better understanding toward the water chemistry in an advanced boiling water reactor (ABWR), such as the one being constructed in the northern part of Taiwan, and for a safer operation of this ABWR, we conducted a proactive, thorough water chemistry analysis prior to the completion of this reactor in this study. A numerical simulation model for water chemistry analyses in ABWRs has been developed, based upon the core technology we established in the past. This core technology for water chemistry modeling is basically an integration of water radiolysis, thermal-hydraulics, and reactor physics. The model, by the name of DEMACE - ABWR, is an improved version of the original DEMACE model and was used for radiolysis and water chemistry prediction in the Longmen ABWR in Taiwan. Predicted results pertinent to the water chemistry variation and the corrosion behavior of structure materials in the primary coolant circuit of this ABWR under rated-power operation were reported in this paper. (authors)

U.S. experience with hydrogen water chemistry in boiling water reactors

International Nuclear Information System (INIS)

Cowan, R.L.; Head, R.A.; Indig, M.E.; Ruiz, C.P.; Simpson, J.L.

1988-01-01

Hydrogen water chemistry in boiling water reactors is currently being adopted by many utilities in the U.S., with eleven units having completed preimplementation test programs, four units operating permanently with hydrogen water chemistry, and six other units in the process of installing permanent equipment. Intergranular stress corrosion cracking protection is required for the recirculation piping system and other regions of the BWR systems. The present paper explores progress in predicting and monitoring hydrogen water chemistry response in these areas. Testing has shown that impurities can play an important role in hydrogen water chemistry. Evaluation of their effects are also performed. Both computer modeling and in plant measurements show that each plant will respond uniquely to feedwater hydrogen addition. Thus, each plant has its own unique hydrogen requirement for recirculation system protecion. Furthermore, the modeling, and plant measurements show that different regions of the BWR respond differently to hydrogen injection. Thus, to insure protection of components other than the recirculation systems may require more (or less) hydrogen demand than indicated by the recirculation system measurements. In addition, impurities such as copper can play a significant role in establishing hydrogen demand. (Nogami, K.)

Development of water chemistry diagnosis system for BWR primary loop

International Nuclear Information System (INIS)

Nagase, Makoto; Asakura, Yamato; Sakagami, Masaharu; Uchida, Shunsuke; Ohsumi, Katsumi.

1988-01-01

The prototype of a water chemistry diagnosis system for BWR primary loop has been developed. Its purposes are improvement of water chemistry control and reduction of the work burden on plant chemistry personnel. It has three main features as follows. (1) Intensifying the observation of water chemistry conditions by variable sampling intervals based on the on-line measured data. (2) Early detection of water chemistry data trends using a second order regression curve which is calculated from the measured data, and then searching the cause of anomaly if anything (3) Diagnosis of Fe concentration in feedwater using model simulations, in order to lower the radiation level in the primary system. (author)

Operating experience with steam generator water chemistry in Japanese PWR plants

International Nuclear Information System (INIS)

Onimura, K.; Hattori, T.

1991-01-01

Since the first PWR plant in Japan started its commercial operation in 1970, seventeen plants are operating as of the end of 1990. First three units initially applied phosphate treatment as secondary water chemistry control and then changed to all volatile treatment (AVT) due to phosphate induced wastage of steam generator tubing. The other fourteen units operate exclusively under AVT. In Japan, several corrosion phenomena of steam generator tubing, resulted from secondary water chemistry, have been experienced, but occurrence of those phenomena has decreased by means of improvement on impurity management, boric acid treatment and high hydrazine operation. Recently secondary water chemistry in Japanese plants are well maintained in every stage of operation. This paper introduces brief summary of the present status of steam generators and secondary water chemistry in Japan and ongoing activities of investigation for future improvement of reliability of steam generator. History and present status of secondary water chemistry in Japanese PWRs were introduced. In order to get improved water chemistry, the integrity of secondary system equipments is essential and the improvement in water chemistry has been achieved with the improvement in equipments and their usage. As a result of those efforts, present status of secondary water is excellent. However, further development for crevice chemistry monitoring technique and an advanced water chemistry data management system is desired for the purpose of future improvement of reliability of steam generator

Chemistry management of generator stator water system

International Nuclear Information System (INIS)

Sankar, N.; Santhanam, V.S.; Ayyar, S.R.; Umapathi, P.; Jeena, P.; Hari Krishna, K.; Rajendran, D.

2015-01-01

Chemistry management of water cooled turbine generators with hollow copper conductors is very essential to avoid possible re-deposition of released copper oxides on stator windings, which otherwise may cause flow restrictions by partial plugging of copper hollow conductors and impair cooling. The phenomenon which is of more concern is not strictly of corrosion failure, but the consequences caused by the re-deposition of copper oxides that were formed by reaction of copper with oxygen. There were also some Operating experiences (OE) related to Copper oxide fouling in the system resulting shut down/off-line of plants. In Madras Atomic Power Station (MAPS), the turbine generator stator windings are of Copper material and cooled by demineralized water passing through the hollow conductors. The heated water from the stator is cooled by process water. A part of the stator water is continuously passed through a mixed bed polisher to remove any soluble ionic contaminants to maintain the purity of system water and also maintain copper content as low as possible to avoid possible re-deposition of released copper oxides on stator windings. The chemistry regime employed is neutral water with dissolved oxygen content between 1000-2000 ppb. Chemistry management of Stator water system was reviewed to know its effectiveness. Detailed chemical analyses of the spent resins from the polishing unit were carried out in various campaigns which indicated only part exhaustion of the polishing unit resins and reasonably low levels of copper entrapment in the resins, thus highlighting the effectiveness of the in-practice chemistry regime. (author)

Colour chemistry in water

OpenAIRE

Cardona, Maria

2015-01-01

Atmospheric carbon dioxide (CO2) levels have increased dramatically in the last few decades. Famous for causing global warming, CO2 is also resulting in the acidification of seas and oceans. http://www.um.edu.mt/think/colour-chemistry-in-water/

Experience of Ko-Ri Unit 1 water chemistry

International Nuclear Information System (INIS)

Tae Il Lee

1983-01-01

The main focus is placed on operational experience in secondary system water chemistry (especially the steam generator) of the Ko-Ri nuclear power plant Unit 1, Republic of Korea, but primary side chemistry is also discussed. The major concern of secondary water chemistry in a PWR is that the condition of the steam generator be well maintained. Full flow deep bed condensate polishers have recently been installed and operation started in July 1982. Boric acid treatment of the steam generator was stopped and only the all volatile treatment method was used thereafter. A review of steam generator integrity, the chemistry control programme, secondary water quality, etc. is considered to be of great value regarding the operation of Unit 1 and future units now under startup testing or construction in the Republic of Korea. (author)

VGB primary and secondary side water chemistry guidelines for PWR plants

International Nuclear Information System (INIS)

Neder, H.; Wolter, D.; Staudt, U.

2007-01-01

The recent revision of the VGB Water Chemistry Guidelines was issued in 2005 and published in the second half of 2006. These guidelines are based on the primary and secondary side operating chemistry experience with all Siemens designed pressurized water reactors gained since the beginning of the 1980s. These guidelines cover For the primary side chemistry Modified lithium boron chemistry, Zinc chemistry for dose rate reduction, Enriched boric acid (EBA) chemistry for high duty core design For the secondary side chemistry High all-volatile treatment (AVT) chemistry (high pH operation) Oxygen injection in the secondary side Especially for the secondary side chemistry, compared with the water chemistry guidelines of other organizations worldwide, these Guidelines are less stringent, providing more operational flexibility to the plant operation, and can be applied for all new designs of steam generators with egg-crates or broached hole tube supports and with I 690TT or I 800 tubing materials. This paper gives an overview of the 2006 revision of the VGB Water Chemistry Guidelines for PWR plants and describes the fundamental goals of water chemistry operation strategies. In addition, the reasons for the selected control parameters and action levels, to achieve an adequate plant performance, are presented based on the operating experience. (orig.)

Assessment of EPRI water chemistry guidelines for new nuclear power plants

International Nuclear Information System (INIS)

Reid Richard; Kim Karen; McCree, Anisa; Eaker, Richard; Sawochka, Steve; Giannelli, Joe

2012-09-01

Water chemistry control technologies for nuclear power plants have been significantly enhanced over the past few decades to improve material and equipment reliability and fuel performance, and to minimize radionuclide production and transport. Chemistry Guidelines have been developed by the Electric Power Research Institute (EPRI) for currently operating plants and have been intermittently revised over the past twenty-five years for the protection of systems and components and for radiation management. As new plants are being designed for improved safety and increased power production, it is important to ensure that the designs consider implementation of state-of-the-art, industry developed water chemistry controls. In parallel, the industry will need to consider and update water chemistry guidelines as well as plant startup and operational strategies based on the advanced plant designs. EPRI has performed assessments of water chemistry control guidance or assumptions provided in design and licensing documents for several advanced plant designs. These designs include: Westinghouse AP1000 Pressurized Water Reactor AREVA US-EPR Pressurized Water Reactor Mitsubishi Nuclear Energy Systems/Mitsubishi Heavy Industries Advanced Pressurized Water Reactor Korea Hydro and Nuclear Power APR1400 Pressurized Water Reactor Toshiba Advanced Boiling Water Reactor (ABWR) General Electric-Hitachi Economic Simplified Boiling Water Reactor (ESBWR) The intent of these assessments was to identify key design differences in each of the new plant designs relative to the current operating fleet and to identify differences in water chemistry specifications or design assumptions provided in design and licensing documents for the plants in comparison to current EPRI Water Chemistry Guidelines. This paper provides a summary of the key results of these assessments. The fundamental design and operation of the advanced plants is similar to the currently operating fleet. As such, the new plants are

Technical Basis for Water Chemistry Control of IGSCC in Boiling Water Reactors

Science.gov (United States)

Gordon, Barry; Garcia, Susan

Boiling water reactors (BWRs) operate with very high purity water. However, even the utilization of near theoretical conductivity water cannot prevent intergranular stress corrosion cracking (IGSCC) of sensitized stainless steel, wrought nickel alloys and nickel weld metals under oxygenated conditions. IGSCC can be further accelerated by the presence of certain impurities dissolved in the coolant. The goal of this paper is to present the technical basis for controlling various impurities under both oxygenated, i.e., normal water chemistry (NWC) and deoxygenated, i.e., hydrogen water chemistry (HWC) conditions for mitigation of IGSCC. More specifically, the effects of typical BWR ionic impurities (e.g., sulfate, chloride, nitrate, borate, phosphate, etc.) on IGSCC propensities in both NWC and HWC environments will be discussed. The technical basis for zinc addition to the BWR coolant will also provided along with an in-plant example of the most severe water chemistry transient to date.

Secondary-water chemistry at Millstone 2

International Nuclear Information System (INIS)

Putkey, T.A.; Pearl, W.L.; Sawochka, S.G.

1983-04-01

Secondary system chemistry and steam generator corrosion observations at the Millstone 2 pressurized water reactor are summarized. Condenser retubing and retrofit of full-flow condensate polishers led to significant improvements in steam generator blowdown chemistry following observations of denting after one year of operation at elevated blowdown chloride levels. Notwithstanding the chemistry improvements, denting has continued but at a much reduced rate. In addition, extensive pitting of the Alloy 600 tubing between the tubesheet and first support plate has been reported recently

WWER water chemistry related to fuel cladding behaviour

Energy Technology Data Exchange (ETDEWEB)

Kysela, J; Zmitko, M [Nuclear Research Inst. plc., Rez (Czech Republic); Vrtilkova, V [Nuclear Fuel Inst., Prague (Czech Republic)

1997-02-01

Operational experience in WWER primary water chemistry and corrosion related to the fuel cladding is reviewed. Insignificant corrosion of fuel cladding was found which is caused by good corrosion resistance of Zr1Nb material and relatively low coolant temperature at WWER-440 reactor units. The differences in water chemistry control is outlined and an attention to the question of compatibility of Zircaloys with WWER water chemistry is given. Some results of research and development in field of zirconium alloy corrosion behaviour are discussed. Experimental facility for in-pile and out-of-pile cladding material corrosion testing is shown. (author). 14 refs, 5 figs, 3 tabs.

Primary water chemistry of VVERs-operating experience

International Nuclear Information System (INIS)

Kysela, Jan; Zmitko, Milan; Petrecky, Igor

1998-01-01

VVER units are operated in mixed boron-potassium-ammonia water chemistry. Several modifications of the water chemistry, differing in boron-potassium co-ordination and in the way how hydrogen concentration is produced and maintain in the coolant, is used. From the operational experience point of view VVER units do not show any significant problems connected with the primary coolant chemistry. The latest results indicate that dose rate levels are slowly returning to the former ones. An improvement of the radiation situation observed last two years is supported by the surface activity measurements. However, the final conclusion on the radiation situation can be made only after evaluation of the several following cycles. Further investigation is also needed to clarify a possible effect of modified water chemistry and shut-down chemistry on radioactivity build-up and dose rate level at Dukovany units. Structure materials composition has a significant effect on radiation situation in the units. It concerns mainly of cobalt content in SG material. There is no clear evidence of possible effect of the SG shut-down regimes on the radiation situation in the units even if the dose rate and surface activity data show wide spread for the individual reactor loops. (S.Y.)

Coolant circuit water chemistry of the Paks Nuclear Power Plant

International Nuclear Information System (INIS)

Tilky, Peter; Doma, Arpad

1985-01-01

The numerous advantages of the proper selection of water chemistry parameters including low corrosion rate of the structural materials, hence the low-level activity build-up, depositions, radiation doses were emphasized. Major characteristics of water chemistry applied to the primary coolant of pressurized water reactors including neutral, slightly basic and strong basic ones are discussed. Boric acid is widely used to control reactivity. Primary coolant water chemistry of WWER type reactors which is based on the addition of ammonia and potassium hydroxide to boric acid is compared with that of other reactors. The demineralization of the total condensate of the steam turbines became a general trend in the water chemistry of the secondary coolant circuits. (V.N.)

Modeling UTLS water vapor: Transport/Chemistry interactions

International Nuclear Information System (INIS)

Gulstad, Line

2005-01-01

This thesis was initially meant to be a study on the impact on chemistry and climate from UTLS water vapor. However, the complexity of the UTLS water vapor and its recent changes turned out to be a challenge by it self. In the light of this, the overall motivation for the thesis became to study the processes controlling UTLS water vapor and its changes. Water vapor is the most important greenhouse gas, involved in important climate feedback loops. Thus, a good understanding of the chemical and dynamical behavior of water vapor in the atmosphere is crucial for understanding the climate changes in the last century. Additionally, parts of the work was motivated by the development of a coupled climate chemistry model based on the CAM3 model coupled with the Chemical Transport Model Oslo CTM2. The future work will be concentrated on the UTLS water vapor impact on chemistry and climate. We are currently studying long term trends in UTLS water vapor, focusing on identification of the different processes involved in the determination of such trends. The study is based on natural as well as anthropogenic climate forcings. The ongoing work on the development of a coupled climate chemistry model will continue within our group, in collaboration with Prof. Wei-Chyung Wang at the State University of New York, Albany. Valuable contacts with observational groups are established during the work on this thesis. These collaborations will be continued focusing on continuous model validation, as well as identification of trends and new features in UTLS water vapor, and other tracers in this region. (Author)

Exoplanetary Atmospheres—Chemistry, Formation Conditions, and Habitability

Science.gov (United States)

Agúndez, Marcelino; Moses, Julianne I; Hu, Yongyun

2016-01-01

Characterizing the atmospheres of extrasolar planets is the new frontier in exoplanetary science. The last two decades of exoplanet discoveries have revealed that exoplanets are very common and extremely diverse in their orbital and bulk properties. We now enter a new era as we begin to investigate the chemical diversity of exoplanets, their atmospheric and interior processes, and their formation conditions. Recent developments in the field have led to unprecedented advancements in our understanding of atmospheric chemistry of exoplanets and the implications for their formation conditions. We review these developments in the present work. We review in detail the theory of atmospheric chemistry in all classes of exoplanets discovered to date, from highly irradiated gas giants, ice giants, and super-Earths, to directly imaged giant planets at large orbital separations. We then review the observational detections of chemical species in exoplanetary atmospheres of these various types using different methods, including transit spectroscopy, Doppler spectroscopy, and direct imaging. In addition to chemical detections, we discuss the advances in determining chemical abundances in these atmospheres and how such abundances are being used to constrain exoplanetary formation conditions and migration mechanisms. Finally, we review recent theoretical work on the atmospheres of habitable exoplanets, followed by a discussion of future outlook of the field. PMID:28057962

Exoplanetary Atmospheres-Chemistry, Formation Conditions, and Habitability.

Science.gov (United States)

Madhusudhan, Nikku; Agúndez, Marcelino; Moses, Julianne I; Hu, Yongyun

2016-12-01

Characterizing the atmospheres of extrasolar planets is the new frontier in exoplanetary science. The last two decades of exoplanet discoveries have revealed that exoplanets are very common and extremely diverse in their orbital and bulk properties. We now enter a new era as we begin to investigate the chemical diversity of exoplanets, their atmospheric and interior processes, and their formation conditions. Recent developments in the field have led to unprecedented advancements in our understanding of atmospheric chemistry of exoplanets and the implications for their formation conditions. We review these developments in the present work. We review in detail the theory of atmospheric chemistry in all classes of exoplanets discovered to date, from highly irradiated gas giants, ice giants, and super-Earths, to directly imaged giant planets at large orbital separations. We then review the observational detections of chemical species in exoplanetary atmospheres of these various types using different methods, including transit spectroscopy, Doppler spectroscopy, and direct imaging. In addition to chemical detections, we discuss the advances in determining chemical abundances in these atmospheres and how such abundances are being used to constrain exoplanetary formation conditions and migration mechanisms. Finally, we review recent theoretical work on the atmospheres of habitable exoplanets, followed by a discussion of future outlook of the field.

Biogeochemical processes in a clay formation in situ experiment: Part E - Equilibrium controls on chemistry of pore water from the Opalinus Clay, Mont Terri Underground Research Laboratory, Switzerland

Energy Technology Data Exchange (ETDEWEB)

Pearson, F.J., E-mail: fjpearson@gmail.com [Ground-Water Geochemistry, 5108 Trent Woods Dr., New Bern, NC 28562 (United States); Tournassat, Christophe; Gaucher, Eric C. [BRGM, B.P. 36009, 45060 Orleans Cedex 2 (France)

2011-06-15

Highlights: > Equilibrium models of water-rock reactions in clay rocks are reviewed. > Analyses of pore waters of the Opalinus Clay from boreholes in the Mont Terri URL, Switzerland, are tabulated. > Results of modelling with various mineral controls are compared with the analyses. > Best agreement results with calcite, dolomite and siderite or daphnite saturation, Na-K-Ca-Mg exchange and/or kaolinite, illite, quartz and celestite saturation. > This approach allows calculation of the chemistry of pore water in clays too impermeable to yield water samples. - Abstract: The chemistry of pore water (particularly pH and ionic strength) is an important property of clay rocks being considered as host rocks for long-term storage of radioactive waste. Pore waters in clay-rich rocks generally cannot be sampled directly. Instead, their chemistry must be found using laboratory-measured properties of core samples and geochemical modelling. Many such measurements have been made on samples from the Opalinus Clay from the Mont Terri Underground Research Laboratory (URL). Several boreholes in that URL yielded water samples against which pore water models have been calibrated. Following a first synthesis report published in 2003, this paper presents the evolution of the modelling approaches developed within Mont Terri URL scientific programs through the last decade (1997-2009). Models are compared to the composition of waters sampled during dedicated borehole experiments. Reanalysis of the models, parameters and database enabled the principal shortcomings of the previous modelling efforts to be overcome. The inability to model the K concentrations correctly with the measured cation exchange properties was found to be due to the use of an inappropriate selectivity coefficient for Na-K exchange; the inability to reproduce the measured carbonate chemistry and pH of the pore waters using mineral-water reactions alone was corrected by considering clay mineral equilibria. Re

Water chemistry and behavior of materials in PWRs and BWRs

Energy Technology Data Exchange (ETDEWEB)

Aaltonen, P; Hanninen, H [VTT Manufacturing Technology, Espoo (Finland)

1997-09-01

Water chemistry plays a major role in corrosion and in activity transport in NPP`s. Although a full understanding of all mechanisms involved in corrosion does not exist, controlling of the water chemistry has achieved good results in recent years. Water chemistry impacts upon the operational safety of LWR`s in two main ways: integrity of pressure boundary materials and, activity transport and out-of-core radiation fields. This paper will describe application of water chemistry control in operating reactors to prevent corrosion. Some problems experienced in LWR`s will be reviewed for the design of the nuclear heating reactors (NHR). (author). 18 refs, 10 figs, 5 tabs.

Water chemistry and behavior of materials in PWRs and BWRs

International Nuclear Information System (INIS)

Aaltonen, P.; Hanninen, H.

1997-01-01

Water chemistry plays a major role in corrosion and in activity transport in NPP's. Although a full understanding of all mechanisms involved in corrosion does not exist, controlling of the water chemistry has achieved good results in recent years. Water chemistry impacts upon the operational safety of LWR's in two main ways: integrity of pressure boundary materials and, activity transport and out-of-core radiation fields. This paper will describe application of water chemistry control in operating reactors to prevent corrosion. Some problems experienced in LWR's will be reviewed for the design of the nuclear heating reactors (NHR). (author). 18 refs, 10 figs, 5 tabs

Chemistry of the water in thermal power plants

International Nuclear Information System (INIS)

Freier, R.K.

1984-01-01

This textbook and practical manual gives a comprehensive review of the scientific knowledge of water as operating substance and of the chemistry of water in thermal power plants. The fundamentals of water chemistry and of the conventional and nuclear water/steam circuit are described. The contents of the chapters are: 1. The atom, 2. The chemical bond, 3. The dissolving capacity of water, 4. Operational parameters and their measurement, 5. Corrosion, 6. The water/steam coolant loop of conventional plants (WSC), 7. The pressurized water reactor (PWR), 8. The boiling water reactor (BWR), 9. The total and partial desalination properties of ion exchangers, 10. The cooling water, 11. The failure of Harrisburg in a simple presentation. (HK) [de

Coupling between water chemistry and thermal output at unsaturated repositories

International Nuclear Information System (INIS)

Walton, J.; LeMone, D.; Casey, D.

1995-01-01

This paper summarizes issues in predicting thermohydrology in the near field of a deep geological repository and the implications for performance assessment. Predicted thermohydrology depends on waste package design, and particularly on backfill materials. The coupling between solute concentrations and thermal gradients leads to a prediction of highly variable water chemistry in the near field which is radically different than the initial, undisturbed water chemistry; however, most analyses to date assume that waste package chemistry is approximately the same as initial pore water chemistry. Several alternative, simplified approaches for performance assessment are discussed

Areva's water chemistry guidebook with chemistry guidelines for next generation plants (AREVA EPRTM reactors)

International Nuclear Information System (INIS)

Ryckelynck, N.; Chahma, F.; Caris, N.; Guillermier, P.; Brun, C.; Caron-Charles, M.; Lamanna, L.; Fandrich, J.; Jaeggy, M.; Stellwag, B.

2012-09-01

Over the years, AREVA globally has maintained a strong expertise in LWR water chemistry and has been focused on minimizing short-term and long-term detrimental effects of chemistry for startup, operation and shutdown chemistry for all key plant components (material integrity and reliability, promote optimal thermal performances, etc.) and fuel. Also AREVA is focused on minimizing contamination and equipment/plant dose rates. Current Industry Guidelines (EPRI, VGB, etc.) provide utilities with selected chemistry guidance for the current operating fleet. With the next generation of PWR plants (e.g. AREVA's EPR TM reactor), materials of construction and design have been optimized based on industry lessons learned over the last 50+ years. To support the next generation design, AREVA water chemistry experts, have subsequently developed a Chemistry Guidebook with chemistry guidelines based on an analysis of the current international practices, plant operating experience, R and D data and calculation codes now available and/or developed by AREVA. The AREVA LWR chemistry Guidebook can be used to help resolve utility and safety authority questions and addresses regulation requirement questions/issues for next generation plants. The Chemistry Guidebook provides water chemistry guidelines for primary coolant, secondary side circuit and auxiliary systems during startup, normal operation and shutdown conditions. It also includes conditioning and impurity limits, along with monitoring locations and frequency requirements. The Chemistry Guidebook Guidelines will be used as a design reference for AREVA's next generation plants (e.g. EPR TM reactor). (authors)

Characterisation of the inorganic chemistry of surface waters in ...

African Journals Online (AJOL)

The main purpose of this study was to determine a simple inorganic chemistry index that can be used for all surface waters in South Africa, in order to characterise the inorganic chemistry of surface waters. Water quality data collected up until 1999 from all sample monitoring stations (2 068 monitoring stations, 364 659 ...

Water chemistry at RBMK plants: Problems and solutions

International Nuclear Information System (INIS)

Mamet, V.; Yurmanov, V.

2002-01-01

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 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 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 25 maintenance in a slightly acid area. (authors)

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)

Physics and Chemistry of Star and Planet Formation in the Alma ERA

Science.gov (United States)

Bergin, Edwin

2014-06-01

ALMA will open up new avenues of exploration encompassing the wide range of star formation in our galaxy and peering into the central heart of planet-forming circumstellar disks. As we seek to explore the origins of stars and planets molecular emission will be at the front and center of many studies probing gas physics and chemistry. In this talk I will discus some of the areas where we can expect significant advances due to the increased sensitivity and superb spatial resolution of ALMA. In star-forming cores, a rich chemistry is revealed that may be the simpler molecular precursors to more complex organics, such as amino acids, seen within primitive rocks in our own solar system. ALMA will provide new information regarding the relative spatial distribution within a given source for a host of organics, sampling tens to hundreds of transitions of a variety of molecules, including presumably new ones. In this area there is a rich synergy with existing ground and space-based data, including Herschel/Spitzer. Here the increased sampling of sources to be enabled by ALMA should bring greater clarity toward the key products of interstellar chemistry and further constrain processes. On smaller Solar System scales, for over a decade most observations of planet-forming disks focused on the dust thermal continuum emission as a probe of the gas content and structure. ALMA will enable reliable and direct studies of gas to explore the evolving physics of planet-formation, the gas dissipation timescales (i.e. the upper limit to the timescale for giant planet birth), and also the chemistry. It is this chemistry that sets the composition of gas giants and also influences the ultimate composition of water and organic materials that are delivered to terrestrial worlds. Here I will show how we can use molecular emission to determine the gas thermal structure of a disk system and the total gas content - key astrophysical quantities. This will also enable more constrained chemical

Safety aspects of water chemistry in light water reactors

International Nuclear Information System (INIS)

1988-12-01

The goals of the water chemistry control programmes are to maximize operational safety and the availability and operating life of primary system components, to maximize fuel integrity, and to control radiation buildup. To achieve these goals an effective corporate policy should be developed and implemented. Essential management responsibilities are: Recognizing of the long-term benefits of avoiding or minimizing: a) system corrosion; b) fuel failure; and c) radiation buildup. The following control or diagnostic parameters are suitable performance indicators: for PWR primary coolant circuits: pH of reactor water (by operating temperature); Concentration of chlorides in reactor water; Hydrogen (or oxygen) in reactor water. For PWR secondary coolant circuits: pH in feedwater; Cation productivity in steam generator blowdown; Iron concentration in feedwater; Oxygen concentration in condensate. And BWR coolant circuits: Conductivity of reactor water; Concentration of chlorides in reactor water; Iron concentration in feedwater; Copper concentration in feedwater. The present document represents a review of the developments in some Member States on how to implement a reasonable water chemistry programme and how to assess its effectiveness through numerical indicators. 12 figs, 20 tabs

Water chemistry

International Nuclear Information System (INIS)

Hofstetter, K.J.; Baston, V.F.

1986-01-01

Prior to the accident, the coolants in the primary and secondary systems were within normal chemistry specifications for an operating pressurized water reactor with once-through steam generators. During and immediately after the accident, additional boric acid and sodium hydroxide were added to the primary coolant for control of criticality and radioiodine solubility. A primary to secondary leak developed contaminating the water in one steam generator. For about 5 years after the accident, the primary coolant was maintained at 3800 +. 100 ppm boron and 1000 +. 100 ppm sodium concentrations. Dissolved oxygen was maintained 7.5, corrosion caused by increased dissolved oxygen levels (up to 8 ppm) and higher chloride ion content (up to 5 ppm) is minimized. Chemical control of dissolved oxygen was discontinued and the coolant was processed. Prior to removal of the reactor vessel head, the boron concentration in the coolant was increased to ≅ 5000 ppm to support future defueling operations. Decontamination of the accident generated water is described in terms of contaminated water management. In addition, the decontamination and chemical lay-up conditions for the secondary system are presented along with an overview of chemical management at TMI-2

Effect of Water Chemistry Factors on Flow Accelerated Corrosion : pH, DO, Hydrazine

International Nuclear Information System (INIS)

Lee, Eun Hee; Kim, Kyung Mo; Kim, Hong Pyo

2013-01-01

Flow accelerated corrosion(FAC) of the carbon steel piping in pressurized water reactors(PWRs) has been major issue in nuclear industry. Severe accident at Surry Unit 2 in 1986 initiated the worldwide interest in this area. Major parameters influencing FAC are material composition, microstructure, water chemistry, and hydrodynamics. Qualitative behaviors of FAC have been well understood but quantitative data about FAC have not been published for proprietary reason. In order to minimize the FAC in PWRs, the optimal method is to control water chemistry factors. Chemistry factors influencing FAC such as pH, corrosion potential, and hydrazine contents were reviewed in this paper. FAC rate decreased with pH up to 10 because magnetite solubility decreased with pH. Corrosion potential is generally controlled dissolved oxygen (DO) and hydrazine in secondary water. DO increased corrosion potential. FAC rate decreased with DO by stabilizing magnetite at low DO concentration or by formation of hematite at high DO concentration. Even though hydrazine is generally used to remove DO, hydrazine itself thermally decomposed to ammonia, nitrogen, and hydrogen raising pH. Hydrazine could react with iron and increased FAC rate. Effect of hydrazine on FAC is rather complex and should be careful in FAC analysis. FAC could be managed by adequate combination of pH, corrosion potential, and hydrazine

Variability in chemistry of surface and soil waters of an ...

African Journals Online (AJOL)

Water chemistry is important for the maintenance of wetland structure and function. Interpreting ecological patterns in a wetland system therefore requires an in-depth understanding of the water chemistry of that system. We investigated the spatial distribution of chemical solutes both in soil pore water and surface water, ...

PWR water chemistry controls: a perspective on industry initiatives and trends relative to operating experience and the EPRI PWR water chemistry guidelines

International Nuclear Information System (INIS)

Fruzzetti, K.; Choi, S.; Haas, C.; Pender, M.; Perkins, D.

2010-01-01

An effective PWR water chemistry control program must address the following goals: Minimize materials degradation (e.g., PWSCC, corrosion of fuel, corrosion damage of steam generator (SG) tubes); Maintain fuel integrity and good performance; Minimize corrosion product transport (e.g., transport and deposition on the fuel, transport into the SGs where it can foul tube surfaces and create crevice environments for the concentration of corrosive impurities); Minimize dose rates. Water chemistry control must be optimized to provide overall improvement considering the sometimes variant constraints of the goals listed above. New technologies are developed for continued mitigation of materials degradation, continued fuel integrity and good performance, continued reduction of corrosion product transport, and continued minimization of plant dose rates. The EPRI chemistry program, in coordination with other EPRI programs, strives to improve these areas through application of chemistry initiatives, focusing on these goals. This paper highlights the major initiatives and issues with respect to PWR primary and secondary system chemistry and outlines the recent, on-going, and proposed work to effectively address them. These initiatives are presented in light of recent operating experience, as derived from EPRI's PWR chemistry monitoring and assessment program, and EPRI's water chemistry guidelines. (author)

Nitrogen Compounds in Radiation Chemistry

International Nuclear Information System (INIS)

Sims, H.E.; Dey, G.R.; Vaudey, C.E.; Peaucelle, C.; Boucher, J.L.; Toulhoat, N.; Bererd, N.; Koppenol, W.H.; Janata, E.; Dauvois, V.; Durand, D.; Legand, S.; Roujou, J.L.; Doizi, D.; Dannoux, A.; Lamouroux, C.

2009-01-01

Water radiolysis in presence of N 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 2 and moreover in absence of oxygen there is no agreement on the formation or not of nitrogen oxide like NO 2 - and NO 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 2 O saturated aqueous solution'; - V. DAUVOIS: 'Analytical strategy for the study of radiolysis gases'

Experience of water chemistry and radiation levels in Swedish BWRs

International Nuclear Information System (INIS)

Ivars, R.; Elkert, J.

1981-01-01

From the BWR operational experience in Sweden it has been found that the occupational radiation exposures have been comparatively low in an international comparison. One main reason for the favourable conditions is the good water chemistry performance. This paper deals at first with the design considerations of water chemistry and materials selection. Next, the experience of water chemistry and radiation levels are provided. Finally, some methods to further reduce the radiation sources are discussed. (author)

Present status and recent improvements of water chemistry at Russian VVER plants

International Nuclear Information System (INIS)

Mamet, V.; Yurmanov, V.

2001-01-01

Water chemistry is an important contributor to reliable plant operation, safety barrier integrity, plant component lifetime, radiation safety, environmental impact. Primary and secondary water chemistry guidelines of Russian VVER plants have been modified to meet the new safety standards. At present 14 VVER units of different generation are in operation at 5 Russian NPPs. There are eight 4-loop pressurised water reactors VVER-1000 (1000 MWe) and six 6-loop pressurised water reactors VVER-440 (440 MWe). Generally, water chemistry at East European VVER plants (about 40 VVER-440 and VVER-1000 units in Ukraine, Bulgaria, Slovakia, Czech Republic, Hungary, Finland and Armenia) is similar to water chemistry at Russian VVER plants. Due to similar design and structural materials some water chemistry improvements were introduced at East European plants after they has been successfully implemented at Russian plants and vice versa. Some water chemistry improvements will be implemented at modern VVER plants under construction in Ukraine, Slovakia, Czech Republic, Iran, China, India. (R.P.)

Water chemistry: cause and control of corrosion degradation in nuclear power plants

International Nuclear Information System (INIS)

Kain, Vivekanand

2008-01-01

The corrosion degradation of a material is directly determined by the water chemistry, material (composition, fabrication procedure and microstructure) and by the stress/strain in the material under operating conditions. Water chemistry plays an important role in both uniform corrosion and localized forms of corrosion of materials. Once we understand how water chemistry is contributing to corrosion of a material, it is logical to modify/change that water chemistry to control the corrosion degradation. In nuclear power plants, different water chemistries have been used in different components/systems. This paper will cover the origin of corrosion degradation in the Primary Heat Transport system of different reactor types, Steam Generator tubing, secondary circuit pipelines, service water pipelines and auxiliary systems and establish the role of water chemistry in causing corrosion degradation. The history of changes in water chemistry adopted in these systems to control corrosion degradation is also described. It is shown by examples that there is an obvious limitation in changing water chemistry to control corrosion degradation and in those cases, a change of material or change of the state of stresses/fabrication procedure becomes necessary. The role of water chemistry as a causative factor and also as a controlling parameter on particular types of corrosion degradation e.g. stress corrosion cracking, flow accelerated corrosion, pitting, crevice corrosion is illustrated. It will be shown that increase in dissolved oxygen content (due to radiolysis in nuclear reactors) is sufficient to make even the de-mineralized water to cause stress corrosion cracking in Boiling Water Reactors. Hydrogen Water Chemistry (by hydrogen injection) to control dissolved oxygen is shown to control the stress corrosion cracking. However, it is not possible to control dissolved oxygen at all parts of the Boiling Water Reactors. Therefore, a further refinement in terms of noble metal

Some aspects of primary and secondary water chemistry in CANDU reactors

International Nuclear Information System (INIS)

LeSurf, J.E.

1978-09-01

A brief review of the water chemistry in various circuits of CANDU reactors is given. Then, five particular aspects of recent work are highlighted: (i) Radiation Field Growth: in-reactor and out-reactor studies have related water chemistry to corrosion product deposition on fuel sheaths and subsequent contamination of out-core surfaces. (ii) Metal Oxide Solubility: novel techniques are being used to measure the solubilities of metal oxides at primary circuit conditions. (iii) Decontamination: the use of heavy water as coolant in CANDU reactors led to the development of a unique decontamination strategy and technique, called CAN-DECON, which has attracted the attention of operators of light-water reactors. (iv) Steam Generator Corrosion: mathematical modelling of the water chemistry in the bulk and crevice regions of nuclear steam generators, supported by chemical experiments, has shown why sea water ingress from leaking condensers can be damaging, and has provided a rapid way to evaluate alternative boiler water chemistries. (v) Automatic Control of Feedwater Chemistry: on-line automatic chemical analysis and computer control of feedwater chemistry provides All Volatile Treatment for normal operation with pure feedwater, and carefully controlled sodium phosphate addition when there is detectable sea-water ingress from leaking condensers. (author)

Control of water chemistry in operating reactors

International Nuclear Information System (INIS)

Riess, R.

1997-01-01

Water chemistry plays a major role in fuel cladding corrosion and hydriding. Although a full understanding of all mechanisms involved in cladding corrosion does not exist, controlling the water chemistry has achieved quite some progress in recent years. As an example, in PWRs the activity transport is controlled by operating the coolant under higher pH-values (i.e. the ''modified'' B/Li-Chemistry). On the other hand, the lithium concentration is limited to a maximum value of 2 ppm in order to avoid an acceleration of the fuel cladding corrosion. In BWR plants, for example, the industry has learned on how to limit the copper concentration in the feedwater in order to limit CILC (Copper Induced Localized Corrosion) on the fuel cladding. However, economic pressures are leading to more rigorous operating conditions in power reactors. Fuel burnups are to be increased, higher efficiencies are to be achieved, by running at higher temperatures, plant lifetimes are to be extended. In summary, this paper will describe the state of the art in controlling water chemistry in operating reactors and it will give an outlook on potential problems that will arise when going to more severe operating conditions. (author). 3 figs, 6 tabs

Control of water chemistry in operating reactors

Energy Technology Data Exchange (ETDEWEB)

Riess, R [Siemens AG Unternehmensbereich KWU, Erlangen (Germany)

1997-02-01

Water chemistry plays a major role in fuel cladding corrosion and hydriding. Although a full understanding of all mechanisms involved in cladding corrosion does not exist, controlling the water chemistry has achieved quite some progress in recent years. As an example, in PWRs the activity transport is controlled by operating the coolant under higher pH-values (i.e. the ``modified`` B/Li-Chemistry). On the other hand, the lithium concentration is limited to a maximum value of 2 ppm in order to avoid an acceleration of the fuel cladding corrosion. In BWR plants, for example, the industry has learned on how to limit the copper concentration in the feedwater in order to limit CILC (Copper Induced Localized Corrosion) on the fuel cladding. However, economic pressures are leading to more rigorous operating conditions in power reactors. Fuel burnups are to be increased, higher efficiencies are to be achieved, by running at higher temperatures, plant lifetimes are to be extended. In summary, this paper will describe the state of the art in controlling water chemistry in operating reactors and it will give an outlook on potential problems that will arise when going to more severe operating conditions. (author). 3 figs, 6 tabs.

Cycle water chemistry based on film forming amines at power plants: evaluation of technical guidance documents

Science.gov (United States)

Dyachenko, F. V.; Petrova, T. I.

2017-11-01

Efficiency and reliability of the equipment in fossil power plants as well as in combined cycle power plants depend on the corrosion processes and deposit formation in steam/water circuit. In order to decrease these processes different water chemistries are used. Today the great attention is being attracted to the application of film forming amines and film forming amine products. The International Association for the Properties of Water and Steam (IAPWS) consolidated the information from all over the World, and based on the research studies and operating experience of researchers and engineers from 21 countries, developed and authorized the Technical Guidance Document: “Application of Film Forming Amines in Fossil, Combined Cycle, and Biomass Power Plants” in 2016. This article describe Russian and International technical guidance documents for the cycle water chemistries based on film forming amines at fossil and combined cycle power plants.

Primary Water Chemistry Control during a Planned Outage at Bruce Power

International Nuclear Information System (INIS)

Ma, Guoping; Nashiem, Rod; Matheson, Shane; Yabar, Berman; Harper, Bill; Roberts, John G.

2012-09-01

Bruce Power has developed a comprehensive outage water chemistry program, which includes both primary and secondary chemistry requirements during planned outages. The purpose of the program is to emphasize the chemistry requirements during outages and subsequent start-ups in order to maintain the integrity of the systems, minimise activity transport and radiation fields, reduce the Carbon-14 release, and to ensure that the requirements are integrated with the outage management program. Prior to a planned outage, Station Chemical Technical Sections identify outage chemistry requirements to Operations and Outage Planning and ensure that work necessary to correct system chemistry issues is within outage work scope. The outage water chemistry program provides direction for establishing alternative sampling locations as demanded by the system configuration during the outage and identifies outage prerequisites for nuclear system purification capabilities. These requirements are contained in an outage checklist. The paper mainly highlights the primary water chemistry issues and chemistry control strategies during planned outages and discusses challenges and successes. (authors)

What are today's choices for PWRs water chemistry?

International Nuclear Information System (INIS)

Berge, P.

1998-01-01

Water chemistry has always been, from the very beginning of operation of power Pressurized Water Reactors (PWRs), an important factor in determining the integrity of many reactor components. For both the primary and secondary coolant circuits, the parameters to control the quality of the chemistry have been subject to changes in time. These changes were dictated mainly by corrosion problems which required an adjustment of the chemistry, before any modification could be made in the design or the selection of materials for the subsequently built reactors or replacement components. The situation today, despite 40 years of experience, still leaves open different options for the specifications of the chemistry of the circuits. These options are sometimes due to differences in design or materials of the circuits, but more often, to the perception by the plant chemists, of the role of the chemistry on the different phenomena which could affect the operation of their plant. Paul Cohen, who was well known in the nuclear industry for the early development of the chemistry in PWRs in the USA, used to say, 'if the head chemist has changed in a plant, the chemistry will change'. The purpose of this lecture is to discuss some of the options which are offered to the chemist in compliance with the basic principles of the chemistry guidelines. (J.P.N.)

Contribution of water chemistry and fish condition to otolith chemistry: comparisons across salinity environments.

Science.gov (United States)

Izzo, C; Doubleday, Z A; Schultz, A G; Woodcock, S H; Gillanders, B M

2015-06-01

This study quantified the per cent contribution of water chemistry to otolith chemistry using enriched stable isotopes of strontium ((86) Sr) and barium ((137) Ba). Euryhaline barramundi Lates calcarifer, were reared in marine (salinity 40), estuarine (salinity 20) and freshwater (salinity 0) under different temperature treatments. To calculate the contribution of water to Sr and Ba in otoliths, enriched isotopes in the tank water and otoliths were quantified and fitted to isotope mixing models. Fulton's K and RNA:DNA were also measured to explore the influence of fish condition on sources of element uptake. Water was the predominant source of otolith Sr (between 65 and 99%) and Ba (between 64 and 89%) in all treatments, but contributions varied with temperature (for Ba), or interactively with temperature and salinity (for Sr). Fish condition indices were affected independently by the experimental rearing conditions, as RNA:DNA differed significantly among salinity treatments and Fulton's K was significantly different between temperature treatments. Regression analyses did not detect relations between fish condition and per cent contribution values. General linear models indicated that contributions from water chemistry to otolith chemistry were primarily influenced by temperature and secondly by fish condition, with a relatively minor influence of salinity. These results further the understanding of factors that affect otolith element uptake, highlighting the necessity to consider the influence of environment and fish condition when interpreting otolith element data to reconstruct the environmental histories of fish. © 2015 The Fisheries Society of the British Isles.

Water chemistry experience of nuclear power plants in Japan

International Nuclear Information System (INIS)

Ishigure, Kenkichi; Abe, Kenji; Nakajima, Nobuo; Nagao, Hiroyuki; Uchida, Shunsuke.

1989-01-01

Japanese LWRs have experienced several troubles caused by corrosions of structural materials in the past ca. 20 years of their operational history, among which are increase in the occupational radiation exposures, intergranular stress corrosion cracking (IGSCC) of stainless steel piping in BWR, and steam generator corrosion problems in PWR. These problems arised partly from the improper operation of water chemistry control of reactor coolant systems. Consequently, it has been realized that water chemistry control is one of the most important factors to attain high availability and reliability of LWR, and extensive researches and developments have been conducted in Japan to achieve the optimum water chemistry control, which include the basic laboratory experiments, analyses of plant operational data, loop tests in operating plants and computer code developments. As a result of the continuing efforts, the Japanese LWR plants have currently attained a very high performance in their operation with high availability and low occupational radiation exposures. A brief review is given here on the R and D of water chemistry in Japan. (author)

Influence of water chemistry on fuel cladding behaviour. Proceedings of a technical committee meeting

International Nuclear Information System (INIS)

1997-02-01

For the purpose of the meeting water chemistry included the actual practice, the water chemistry monitoring and the on-going research. Corrosion included also hydriding, recent observations made in reactors, modelling and the recent research carried out. Fifty seven participants representing twenty countries attended the thirty formal presentations and the subsequent discussions. The thirty papers presented were split into five sessions covering, Reactor experience, Mechanism and Modelling, Oxidation and hydriding, On-line monitoring of water chemistry and the review of existing and advanced water chemistries. Four panel discussions including ''Corrosion mechanism and Modelling'', ''Corrosion and Hydriding'', ''Plant Experience and Loop Experiments'', Water Chemistry, Current Practice and Emerging Solutions'' and ''On-line Monitoring of Water Chemistry and Corrosion'' were organized. The main points of discussion focussed on the optimization of water chemistry, the compatibility of potassium water chemistry with the utilization of Zircaloy 4 or the utilization of zirconium niobium cladding with lithium water chemistry. The effect of the fabrication route and of the cladding composition (Sn content) on the corrosion kinetics, the state of the art and the correlative gaps in cladding corrosion modelling and the recent developments of on-line monitoring of water chemistry together with examination of suitable developments, were also discussed. Refs, figs, tabs

Influence of water chemistry on fuel cladding behaviour. Proceedings of a technical committee meeting

Energy Technology Data Exchange (ETDEWEB)

NONE

1997-02-01

For the purpose of the meeting water chemistry included the actual practice, the water chemistry monitoring and the on-going research. Corrosion included also hydriding, recent observations made in reactors, modelling and the recent research carried out. Fifty seven participants representing twenty countries attended the thirty formal presentations and the subsequent discussions. The thirty papers presented were split into five sessions covering, Reactor experience, Mechanism and Modelling, Oxidation and hydriding, On-line monitoring of water chemistry and the review of existing and advanced water chemistries. Four panel discussions including ``Corrosion mechanism and Modelling``, ``Corrosion and Hydriding``, ``Plant Experience and Loop Experiments``, Water Chemistry, Current Practice and Emerging Solutions`` and ``On-line Monitoring of Water Chemistry and Corrosion`` were organized. The main points of discussion focussed on the optimization of water chemistry, the compatibility of potassium water chemistry with the utilization of Zircaloy 4 or the utilization of zirconium niobium cladding with lithium water chemistry. The effect of the fabrication route and of the cladding composition (Sn content) on the corrosion kinetics, the state of the art and the correlative gaps in cladding corrosion modelling and the recent developments of on-line monitoring of water chemistry together with examination of suitable developments, were also discussed. Refs, figs, tabs.

BWR chemistry control status: a summary of industry chemistry status relative to the BWR water chemistry guidelines

International Nuclear Information System (INIS)

Garcia, S.E.; Giannelli, J.F.; Jarvis, M.L.

2010-01-01

The EPRI Boiling Water Reactor (BWR) Water Chemistry Guidelines were revised and issued in October 2008. The 2008 Revision of the Guidelines continues to focus on intergranular stress corrosion cracking (IGSCC), which can limit the service life of susceptible materials and components exposed to water chemistry environments. The 2008 Revision also places increased emphasis on fuel performance and meeting the industry goal of zero fuel failures by 2010. As an industry consensus document, the Guidelines were created to provide proactive water chemistry control strategies for mitigating IGSCC, maintaining fuel integrity and controlling radiation fields. The Guidelines provide a technically-based framework for an effective BWR water chemistry program. This paper provides an overview of industry experience relative to the Guidelines. Over the past few years, many BWR units have implemented noble metal chemical application technologies either during plant hot or cold shutdown or at normal power operating conditions. This paper explores plant experience with optimized water chemistry, implementation of various additive chemistries such as noble metal application and zinc addition, and compliance with the Guidelines recommendations. Depleted zinc oxide addition has been broadly applied across the BWR fleet since the 1980s. The guidance for zinc addition has been revised in the Guidelines to reflect concerns with fuel performance. While zinc addition is a successful method for shutdown dose rate control, concerns still exist for high zinc deposition on fuel surfaces, especially when feedwater iron is elevated and as fuel cores are being driven to provide maximum power output over longer fuel cycles. Recent plant experience has shown that the utilization of online noble metal application and continued zinc addition may provide additional benefits for radiation control. Dose rate experiences at plants utilizing the online noble metal application technology and zinc addition

BWR chemistry control status: a summary of industry chemistry status relative to the BWR water chemistry guidelines

Energy Technology Data Exchange (ETDEWEB)

Garcia, S.E., E-mail: sgarcia@epri.com [Electric Power Research Inst. (EPRI), Palo Alto, California (United States); Giannelli, J.F.; Jarvis, M.L., E-mail: jgiannelli@finetech.com [Finetech, Inc., Parsippany, NJ (United States)

2010-07-01

The EPRI Boiling Water Reactor (BWR) Water Chemistry Guidelines were revised and issued in October 2008. The 2008 Revision of the Guidelines continues to focus on intergranular stress corrosion cracking (IGSCC), which can limit the service life of susceptible materials and components exposed to water chemistry environments. The 2008 Revision also places increased emphasis on fuel performance and meeting the industry goal of zero fuel failures by 2010. As an industry consensus document, the Guidelines were created to provide proactive water chemistry control strategies for mitigating IGSCC, maintaining fuel integrity and controlling radiation fields. The Guidelines provide a technically-based framework for an effective BWR water chemistry program. This paper provides an overview of industry experience relative to the Guidelines. Over the past few years, many BWR units have implemented noble metal chemical application technologies either during plant hot or cold shutdown or at normal power operating conditions. This paper explores plant experience with optimized water chemistry, implementation of various additive chemistries such as noble metal application and zinc addition, and compliance with the Guidelines recommendations. Depleted zinc oxide addition has been broadly applied across the BWR fleet since the 1980s. The guidance for zinc addition has been revised in the Guidelines to reflect concerns with fuel performance. While zinc addition is a successful method for shutdown dose rate control, concerns still exist for high zinc deposition on fuel surfaces, especially when feedwater iron is elevated and as fuel cores are being driven to provide maximum power output over longer fuel cycles. Recent plant experience has shown that the utilization of online noble metal application and continued zinc addition may provide additional benefits for radiation control. Dose rate experiences at plants utilizing the online noble metal application technology and zinc addition

Primary water chemistry for NPP with VVER-TOI

International Nuclear Information System (INIS)

Susakin, S.N.; Brykov, S.I.; Zadonsky, N.V.; Bystrova, O.S.

2012-09-01

Nowadays within the framework of development of the nuclear power industry in Russia the VVER-TOI reactor is under designing (Standard optimized design). The given design provides for improvement of operation safety level, of technical-economic, operational and load-follow characteristics, and for the raise of competitive capacity of reactor plant and NPP as a whole. In VVER-TOI reactor plant design the primary water chemistry has been improved considering operation experience of VVER reactor plants and a possibility of RP operation under load-follow modes from the viewpoint of meeting the following requirements: - suppression of generation of oxidizing radiolytic products under power operation; - assurance of corrosion resistance of structural materials of equipment and pipelines throughout the NPP design service life; - minimization of deposits on surfaces of the reactor core fuel rods and on heat exchange surface of steam generators; - minimization of accumulation of activated corrosion products; - minimization of the amount of radioactive processing waste. In meeting these requirements an important role is devoted to suppression of generation of oxidizing radiolytic products owing to accumulation of hydrogen in the primary coolant. At NPP with VVER-1000 reactor the ammonia-potassium water chemistry is used wherein the hydrogen accumulation is provided at the expense of ammonia proportioning. Usage of ammonia leads to generation of additional amount of radioactive processing waste and to increased irregularity of maintaining the water chemistry under the daily load-follow modes. In VVER TOI design the primary water chemistry is improved by replacing the proportioning of ammonia with the proportioning of gaseous hydrogen. Different process schemes were considered that provide for a possibility of hydrogen accumulation and maintaining owing to direct proportioning of gaseous hydrogen. The obtained results showed that transition to the potassium water chemistry

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.

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)

1998-12-31

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.

Development of a diagnostic expert system for secondary water chemistry

International Nuclear Information System (INIS)

Suganuma, S.; Ishikawa, S.; Kato, A.; Yamauchi, S.; Hattori, T.; Yoshikawa, T.; Miyamoto, S.

1990-01-01

Water chemistry control for the secondary side of the PWR plants is one of the most important tasks for maintaining the reliability of plant equipment and for extending the operating life of the plant. Water chemistry control should be maintained according to the plant chemist' considered judgement which is based on continual experienced observation. Mitsubishi Heavy Industries (MHI) has been developing a comprehensive data management and diagnosis system, which continuously observes the secondary water chemistry data with on-line monitors, immediately diagnosing causes whenever any symptoms of abnormality are detected and does the necessary data management, in order to support plant staff to controll water chemistry. This system has the following three basic functions: data management, diagnosis and simulation. This paper presents the outline of the total system, and then describes in detail the procedure of diagnosis, the structure of the knowledge and its validation process

On the mechanism of water cluster-ion formation in carbon dioxide

International Nuclear Information System (INIS)

Warneck, P.; Rakshit, A.B.

1981-01-01

A drift chamber mass spectrometer has been used to study the formation of water cluster-ions in carbon dioxide containing traces of water vapour. The dominant reaction sequences were identified up to the fourth generation of daughter ions starting with CO 2 + . The subsequent reaction mechanism remains uncertain and several possibilities are discussed. The final ions are H 3 O + H 2 O and H 3 O + (H 2 O) 2 . The significance of the reaction schemes to the radiation chemistry of carbon dioxide is pointed out. (orig.)

Water chemistry - one of the key technologies for safe and reliable nuclear power plant operation

International Nuclear Information System (INIS)

Uchida, S.; Otoha, K.; Ishigure, K.

2006-01-01

Full text: Full text: Water chemistry control is one of the key technologies to establish safe and reliable operation of nuclear power plants. Continuous and collaborative efforts of plant manufacturers and plant operator utilities have been focused on optimal water chemistry control, for which, a trio of requirements for water chemistry, a) better reliability of reactor structures and fuels, b) lower occupational exposure, and c) fewer radwaste sources, should be simultaneously satisfied. The research committee related to water chemistry of the Atomic Energy Society of Japan has played important roles to enhance improvement in water chemistry control, to share knowledge and experience with water chemistry among plant operators and manufacturers, to establish common technological bases for plant water chemistry and then to transfer them to the next generation related to water chemistry. Furthermore, the committee has tried to contribute to arranging R and D proposals for further improvement in water chemistry control through road map planning

Water chemistry control practices and data of the European BWR fleet

International Nuclear Information System (INIS)

Stellwag, B.; Laendner, A.; Weiss, S.; Huettner, F.

2010-01-01

Nineteen BWR plants are in operation in Europe, nine built by ASEA Atom, six by Siemens KWU and four by General Electric. This paper gives an overview of water chemistry operation practices and parameters of the European BWR plants. General design characteristics of the plants are described. Chemistry control strategies and underlying water chemistry guidelines are summarized. Chemistry data are presented and discussed with regard to plant design characteristics. The paper is based on a contract of the European BWR Forum with AREVA on a chemistry sourcebook for member plants. The survey of chemistry data was conducted for the years 2002 to 2008. (author)

Reactor water chemistry control

International Nuclear Information System (INIS)

Kundu, A.K.

2010-01-01

Tarapur Atomic Power Station - 1 and 2 (TAPS) is a twin unit Boiling Water Reactors (BWRs) built in 1960's and operating presently at 160MWe. TAPS -1 and 2 are one of the vintage reactors operating in the world and belongs to earlier generation of BWRs has completed 40 years of successful, commercial and safe operation. In 1980s, both the reactors were de-rated from 660MWth to 530MWth due to leaks in the Secondary Steam Generators (SSGs). In BWR the feed water acts as the primary coolant which dissipates the fission heat and thermalises the fast neutrons generated in the core due to nuclear fission reaction and under goes boiling in the Reactor Pressure Vessel (RPV) to produce steam. Under the high reactor temperature and pressure, RPV and the primary system materials are highly susceptible to corrosion. In order to avoid local concentration of the chemicals in the RPV of BWR, chemical additives are not recommended for corrosion prevention of the system materials. So to prevent corrosion of the RPV and the primary system materials, corrosion resistant materials like stainless steel (of grade SS304, SS304L and SS316LN) is used as the structural material for most of the primary system components. In case of feed water system, main pipe lines are of carbon steel and the heater shell materials are of carbon steel lined with SS whereas the feed water heater tubes are of SS-304. In addition to the choice of materials, another equally important factor for corrosion prevention and corrosion mitigation of the system materials is maintaining highly pure water quality and strict water chemistry regime for both the feed water and the primary coolant, during operation and shutdown of the reactor. This also helps in controlled migration of corrosion product to and from the reactor core and to reduce radiation field build up across the primary system materials. Experience in this field over four decades added to the incorporation of modern techniques in detection of low

A prototype expert system 'SMART' for water chemistry control in reactor water circuits

International Nuclear Information System (INIS)

Rangarajan, S.; Narasimhan, S.V.

1998-01-01

The operational safety of a power plant depends mainly on the material compatibility of the system materials with the environment. However, for an operating plant, the material is almost fixed and hence one can improve the safety by controlling the surrounding environment. From the economy point of view, the plant availability factor as well as plant life extension (PLEX) are important considerations and these necessitate a systematic approach for continuous parametric monitoring, rapid data analysis and diagnosis for controlling the water chemistry regime. A prototype expert system 'SMART' was developed in BASIC language. The expert system consists of four modules. The DATA HANDLER module controls all the data handling functions and graphical display of the data parameters. It also generates weekly and monthly reports of the water chemistry data. The DATA INTERPRETER module compares the experimental data with the theoretically calculated values and predicts the presence of impurity ingress in the system. The CHEMISTRY EXPERT contains the knowledge base about the various sub-systems. All the water chemistry specifications are translated in the form of IF... THEN.. rules and are stored in this module. The expert system inferences with the forward chain reasoning mechanism to identify the diagnostic parameters by consulting the knowledge base and applying the appropriate rules. The ACTION EXPERT module collects all the diagnostic parameters and suggests the operator, the remedial actions/counter measures that should be taken immediately. This rule based system can be expanded to accommodate different water chemistry regimes. (author)

The secondary water chemistry and its quality specification of PWR steam generators

International Nuclear Information System (INIS)

Zhang Guiqin.

1984-01-01

Reasonably organizing the secondary water chemistry of a steam generator is of great importance for improving thermal-hydraulic characteristics and avoiding or alleviating probability of its internals failures by corrosion. In this paper emphasis is put on importance and task of the secondary water chemistry, the meaning and the control demand for feedwater and boiler water specification. At the same time, the current situation on the secondary water chemistry of PWR steam generators is reviewed generally. (Author)

Chemical evolution of formation waters in the Palm Valley gas field, Northern Territory

International Nuclear Information System (INIS)

Andrew, A.S.; Giblin, A.M.

2000-01-01

The chemical composition and evolution of formation waters associated with gas production in the Palm Valley field, Northern Territory, has important implications for reservoir management, saline water disposal, and gas reserve calculations. Historically, the occurrence of saline formation water in gas fields has been the subject of considerable debate. A better understanding of the origin, chemical evolution and movement of the formation water at Palm Valley has important implications for future reservoir management, disposal of highly saline water and accurate gas reserves estimation. Major and trace element abundance data suggest that a significant component of the highly saline water from Palm Valley has characteristics that may have been derived from a modified evaporated seawater source such as an evaporite horizon. The most dilute waters probably represent condensate and the variation in the chemistry of the intermediate waters suggests they were derived from a mixture of the condensate with the highly saline brine. The chemical and isotopic results raise several interrelated questions; the ultimate source of the high salinity and the distribution of apparently mixed compositions. In this context several key observation are highlighted. Strontium concentrations are extremely high in the brines; although broadly similar in their chemistry, the saline fluids are neither homogeneous nor well mixed; the 87 Sr/ 86 Sr ratios in the brines are higher than the signatures preserved in the evaporitic Bitter Springs Formation, and all other conceivably marine-related evaporites (Strauss, 1993); the 87 Sr/ 86 Sr ratios in the brines are lower than those measured from groundmass carbonates in the host rocks, and that the 87 Sr/ 86 Sr ratios of the brines are similar, but still somewhat higher than those measured in vein carbonates from the reservoir. It is concluded that the high salinity brine entered the reservoir during the Devonian uplift and was subsequently

Structural material anomaly detection system using water chemistry data

International Nuclear Information System (INIS)

Asakura, Yamato; Nagase, Makoto; Uchida, Shunsuke; Ohsumi, Katsumi.

1992-01-01

The concept of an advanced water chemistry diagnosis system for detection of anomalies and preventive maintenance of system components is proposed and put into a concrete form. Using the analogy to a medical inspection system, analyses of water chemistry change will make it possible to detect symptoms of anomalies in system components. Then, correlations between water chemistry change and anomaly occurrence in the components of the BWR primary cooling system are analyzed theoretically. These fragmentary correlations are organized and reduced to an algorithm for the on-line diagnosis system using on-line monitoring data, pH and conductivity. By using actual plant data, the on-line diagnosis model system is verified to be applicable for early and automatic finding of the anomaly cause and for timely supply of much diagnostic information to plant operators. (author)

Effect of Formative Quizzes on Teacher Candidates’ Learning in General Chemistry

OpenAIRE

Yalaki, Yalcin; Bayram, Zeki

2015-01-01

Formative assessment or assessment for learning is one of the most emphasized educational innovations around the world. Two of the common strategies that could be used in formative assessment are use of summative tests for formative purposes and comment only marking. We utilized these strategies in the form of formative quizzes in a general chemistry course and measured its effect on students’ learning. The results of our weak-experimental design, which was conducted with 124 pre-service elem...

Carbonate chemistry, water quality, coral measurements

Data.gov (United States)

U.S. Environmental Protection Agency — Carbonate chemistry parameters (pH, total alkalinity, and pCO2), water quality parameters (Temperature, salinity, Ca, Mg, PO4, NH3 and NO3) as well as all coral...

Geochemistry of water in the Fort Union formation of the northern Powder River basin, southeastern Montana

Science.gov (United States)

Lee, Roger W.

1981-01-01

Shallow water in the coal-bearing Paleocene Fort Union Formation of southeastern Montana was investigated to provide a better understanding of its geochemistry. Springs, wells less than 200 feet deep, and wells greater than 200 feet deep were observed to have different water qualities. Overall, the ground water exists as two systems: a mosaic of shallow, chemically dynamic, and localized recharge-discharge cells superimposed on a deeper, chemically static regional system. Water chemistry is highly variable in the shallow system; whereas, waters containing sodium and bicarbonate characterize the deeper system. Within the shallow system, springs and wells less than 200 feet deep show predominantly sodium and sulfate enrichment processes from recharge to discharge. These processes are consistent with the observed aquifer mineralogy and aqueous chemistry. However, intermittent mixing with downward moving recharge waters or upward moving deeper waters, and bacterially catalyzed sulfate reduction, may cause apparent reversals in these processes.

Recent experience in water chemistry control at PWR plants

International Nuclear Information System (INIS)

Makino, Ichiro

2000-01-01

At present, 23 units of PWRs are under operation in all of Japan, among which 11 units are operated by the Kansai Electric Power Co., Inc. (KEP). Plant availability in KEP's PWRs has been improved for the past several years, through their successive stable operation. Recently, a focus is given not only to maintenance of plant integrity, but also to preventive maintenance and water chemistry control. Various measures have been carried out to enhance exposure reduction of the primary water chemistry control in the Japanese PWRs. As a result, environmental dose equivalent rate is decreasing. A secondary system is now under excellent condition because of application of diversified measures for prevention of the SG tube corrosion. At present, the water chemistry control measures which take into account of efficient chemistry control and plant aging deterioration prevention, are being examined to use for both primary and secondary systems in Japanese PWRs, to further enhance their plant integrity and availability. And, some of them are currently being actually applied. (G.K.)

Water chemistry of the JMTR IASCC irradiation loop system

International Nuclear Information System (INIS)

Hanawa, Satoshi; Oogiyanagi, Jin; Mori, Yuichiro; Saito, Junichi; Tsukada, Takashi

2006-01-01

Irradiation assisted stress corrosion cracking (IASCC) is recognized as an important degradation issue of the core-internal material for aged Boiling Water Reactors (BWRs). Therefore, irradiation loop system has been developed and installed in the Japan Materials Testing Reactor to perform the IASCC irradiation test. In the IASCC irradiation test, water chemistry of irradiation field is one of the most important key parameters because it affects initiation and propagation of cracks. This paper summarizes the measurement and evaluation method of water chemistry of IASCC irradiation loop system. (author)

Assessment of EPRI water chemistry guidelines for new nuclear power plants

Energy Technology Data Exchange (ETDEWEB)

Kim, K.; Fruzzetti, K.; Garcia, S. [Electric Power Research Inst., Palo Alto, California (United States); Eaker, R. [Richard W. Eaker, LLC, Matthews, North Carolina (United States); Giannelli, J.; Tangen, J. [Finetech, Inc., Parsippany, New Jersey (United States); Gorman, J.; Marks, C. [Dominion Engineering, Inc., Reston, Virginia (United States); Sawochka, S. [NWT Corp., San Jose, California (United States)

2010-07-01

Water chemistry control technologies for nuclear power plants have been significantly enhanced over the past few decades to improve material and equipment reliability and fuel performance, and to minimize radionuclide production and transport. Chemistry Guidelines have been developed by the Electric Power Research Institute (EPRI) for current operating plants and have been intermittently revised over the past twenty-five years for the protection of systems and components and for radiation management. As new plants are being designed for improved safety and increased power production, it is important to ensure that the designs consider implementation of industry approved water chemistry controls. In parallel, the industry will need to consider and develop updated water chemistry guidelines as well as plant startup and operational strategies based on the advanced plant designs. In 2010, EPRI began to assess chemistry control strategies at advanced plants, based on the Design Control Documents (DCDs), Combined Construction and Operating License Applications (COLA), and operating experiences (where they exist) against current Water Chemistry Guidelines. Based on this assessment, differences between planned chemistry operations at new plants and the current Guidelines will be identified. This assessment will form the basis of future activities to address these differences. The project will also assess and provide, as feasible, water chemistry guidance for startup and hot functional testing of the new plants. EPRI will initially assess the GE-Hitachi/Toshiba ABWR and the Westinghouse AP1000 designs. EPRI subsequently plans to assess other plant designs such as the AREVA U.S. EPR, Mitsubishi Heavy Industries (MHI) U.S. APWR, and GE-Hitachi (GE-H) ESBWR. This paper discusses the 2010 assessments of the ABWR and AP1000. (author)

Assessment of EPRI water chemistry guidelines for new nuclear power plants

International Nuclear Information System (INIS)

Kim, K.; Fruzzetti, K.; Garcia, S.; Eaker, R.; Giannelli, J.; Tangen, J.; Gorman, J.; Marks, C.; Sawochka, S.

2010-01-01

Water chemistry control technologies for nuclear power plants have been significantly enhanced over the past few decades to improve material and equipment reliability and fuel performance, and to minimize radionuclide production and transport. Chemistry Guidelines have been developed by the Electric Power Research Institute (EPRI) for current operating plants and have been intermittently revised over the past twenty-five years for the protection of systems and components and for radiation management. As new plants are being designed for improved safety and increased power production, it is important to ensure that the designs consider implementation of industry approved water chemistry controls. In parallel, the industry will need to consider and develop updated water chemistry guidelines as well as plant startup and operational strategies based on the advanced plant designs. In 2010, EPRI began to assess chemistry control strategies at advanced plants, based on the Design Control Documents (DCDs), Combined Construction and Operating License Applications (COLA), and operating experiences (where they exist) against current Water Chemistry Guidelines. Based on this assessment, differences between planned chemistry operations at new plants and the current Guidelines will be identified. This assessment will form the basis of future activities to address these differences. The project will also assess and provide, as feasible, water chemistry guidance for startup and hot functional testing of the new plants. EPRI will initially assess the GE-Hitachi/Toshiba ABWR and the Westinghouse AP1000 designs. EPRI subsequently plans to assess other plant designs such as the AREVA U.S. EPR, Mitsubishi Heavy Industries (MHI) U.S. APWR, and GE-Hitachi (GE-H) ESBWR. This paper discusses the 2010 assessments of the ABWR and AP1000. (author)

BWR plant-to-fleet water chemistry trends -- Past and present

International Nuclear Information System (INIS)

Baston, V.F.; Sundberg, L.L.; Huff, J.M.

1995-01-01

Good water chemistry control is important for the integrity and satisfactory performance of BWRs. A historical review of selected chemistry performance indicators (e.g., conductivity) illustrates the improved chemistry control today relative to that in the past as well as the ability to evaluate these operational indicators

Real time water chemistry monitoring and diagnostics

International Nuclear Information System (INIS)

Gaudreau, T.M.; Choi, S.S.

2002-01-01

EPRI has produced a real time water chemistry monitoring and diagnostic system. This system is called SMART ChemWorks and is based on the EPRI ChemWorks codes. System models, chemistry parameter relationships and diagnostic approaches from these codes are integrated with real time data collection, an intelligence engine and Internet technologies to allow for automated analysis of system chemistry. Significant data management capabilities are also included which allow the user to evaluate data and create automated reporting. Additional features have been added to the system in recent years including tracking and evaluation of primary chemistry as well as the calculation and tracking of primary to secondary leakage in PWRs. This system performs virtual sensing, identifies normal and upset conditions, and evaluates the consistency of on-line monitor and grab sample readings. The system also makes use of virtual fingerprinting to identify the cause of any chemistry upsets. This technology employs plant-specific data and models to determine the chemical state of the steam cycle. (authors)

Optimization of Water Chemistry to Ensure Reliable Water Reactor Fuel Performance at High Burnup and in Ageing Plant (FUWAC)

International Nuclear Information System (INIS)

2011-10-01

This report presents the results of the Coordinated Research Project (CRP) on Optimization of Water Chemistry to Ensure Reliable Water Reactor Fuel Performance at High Burnup and in Ageing Plants (FUWAC, 2006-2009). It provides an overview of the results of the investigations into the current state of water chemistry practice and concerns in the primary circuit of water cooled power reactors including: corrosion of primary circuit materials; deposit composition and thickness on the fuel; crud induced power shift; fuel oxide growth and thickness; radioactivity buildup in the reactor coolant system (RCS). The FUWAC CRP is a follow-up to the DAWAC CRP (Data Processing Technologies and Diagnostics for Water Chemistry and Corrosion Control in Nuclear Power Plants 2001-2005). The DAWAC project improved the data processing technologies and diagnostics for water chemistry and corrosion control in nuclear power plants (NPPs). With the improved methods for controlling and monitoring water chemistry now available, it was felt that a review of the principles of water chemistry management should be undertaken in the light of new materials, more onerous operating conditions, emergent issues such as CIPS, also known as axial offset anomaly (AOA) and the ageing of operating power plant. In the framework of this CRP, water chemistry specialists from 16 nuclear utilities and research organizations, representing 15 countries, exchanged experimental and operational data, models and insights into water chemistry management. The CD-ROM attached to this IAEA-TECDOC includes the report itself, detailed progress reports of three Research Coordination Meetings (RCMs) (Annexes I-III) and the reports and presentations made during the project by the participants.

Reactor water chemistry relevant to coolant-cladding interaction

International Nuclear Information System (INIS)

1987-09-01

The report is a summary of the work performed in a frame of a Coordinated Research Program organized by the IAEA and carried out from 1981 till 1986. It consists of a survey on our knowledge on coolant-cladding interaction: the basic phenomena, the relevant parameters, their control and the modelling techniques implemented for their assessment. Based upon the results of this Coordinated Research Program, the following topics are reviewed on the report: role of water chemistry in reliable operation of nuclear power plants; water chemistry specifications and their control; behaviour of fuel cladding materials; corrosion product behaviour and crud build-up in reactor circuits; modelling of corrosion product behaviour. This report should be of interest to water chemistry supervisors at the power plants, to experts in utility engineering departments, to fuel designers, to R and D institutes active in the field and to the consultants of these organizations. A separate abstract was prepared for each of the 3 papers included in the Annex of this document. Refs, figs, tabs

Pore-water chemistry effects on the compressibility behaviour of Boom Clay

International Nuclear Information System (INIS)

Deng, Y.F.; Cui, Y.J.; Tang, A.M.; Nguyen, X.P.; Li, X.L.; Maarten, V.G.

2010-01-01

Document available in extended abstract form only. Boom clay is a thick deposit of over-consolidated marine clay, and belongs to the Oligocene series. Its hydraulic conductivity has been investigated since many years in Belgium within the site characterization program related to the performance assessment of potential geological disposal of high-level radioactive waste in this formation. Recently, the work of Wemaere et al. (2008) shows a significant variability of the hydraulic conductivity of the Boom clay. Indeed, they performed measurements on soil cores taken from four distant boreholes at various depths. The vertical hydraulic conductivity was found to vary from 3 x 10 -12 to 10 x 10 -12 m/s. It is suspected that this variability would be partly related to the water chemistry effects. Indeed, De Craen et al. (2006) shows that the pore-water chemical composition of soil cores taken from the Essen site is significantly different from that at the Mol site. If the pore water chemistry has strong effect on the hydraulic conductivity, its effect on the mechanical behaviour needs to be investigated too. The aim of this paper is to verify whether there are significant effects of pore-water chemistry on the soil compressibility. This study would be helpful to transpose the knowledge obtained from the Mol site to other sites of Boom clay formation where the geochemical components are different from the former site, as the hydro-mechanical characteristics of Boom clay at the Mol site has been widely investigated since the last decades. Two soil cores were taken from the Essen site at a depth of 227 m (Ess83) and 240 m (Ess96). Based on the geochemical analysis presented by De Craen et al. (2006), synthetic water having similar chemical composition of the in-situ pore-water was prepared. The identification geotechnical characteristics of these cores are shown in Table 2. It can be observed that the clay content (particle size < 2 μm) is relatively high (more than 50

Water chemistry technology. One of the key technologies for safe and reliable nuclear power plant operation

International Nuclear Information System (INIS)

Uchida, Shunsuke; Katsumura, Yosuke

2013-01-01

Water chemistry control is one of the key technologies to establish safe and reliable operation of nuclear power plants. Continuous and collaborative efforts of plant manufacturers and plant operator utilities have been focused on optimal water chemistry control, for which, a trio of requirements for water chemistry should be simultaneously satisfied: (1) better reliability of reactor structures and fuel rods; (2) lower occupational exposure and (3) fewer radwaste sources. Various groups in academia have carried out basic research to support the technical bases of water chemistry in plants. The Research Committee on Water Chemistry of the Atomic Energy Society of Japan (AESJ), which has now been reorganized as the Division of Water Chemistry (DWC) of AESJ, has played important roles to promote improvements in water chemistry control, to share knowledge about and experiences with water chemistry control among plant operators and manufacturers and to establish common technological bases for plant water chemistry and then to transfer them to the next generation of plant workers engaged in water chemistry. Furthermore, the DWC has tried and succeeded arranging R and D proposals for further improvement in water chemistry control through roadmap planning. In the paper, major achievements in plant technologies and in basic research studies of water chemistry in Japan are reviewed. The contributions of the DWC to the long-term safe management of the damaged reactors at the Fukushima Daiichi Nuclear Power Plant until their decommissioning are introduced. (author)

Sodium-water clusters and their role in radiation chemistry

International Nuclear Information System (INIS)

Dhar, S.; Kestner, N.R.

1988-01-01

Studies of sodium-water clusters are presented which could serve as models for the recently suggested intermediate species in the radiation chemistry of water. The ionization potentials and the lower excited states of sodium with n-water molecules are calculated by ab initio quantum chemistry methods. The ionization potential calculated at the SCF level for the water monomer is 4.10 eV, which becomes 4.34 at the MP2 correlation level. The experimental value is 4.379 ± 0.002 eV. Structural data is presented for the lower members of the sodium with n-water clusters. In addition the Hartree-Fock calculations indicate that there should be some strong charge transfer to solvent transitions at higher energies. (author)

Dynamic combinatorial chemistry with diselenides and disulfides in water

DEFF Research Database (Denmark)

Rasmussen, Brian; Sørensen, Anne; Gotfredsen, Henrik

2014-01-01

Diselenide exchange is introduced as a reversible reaction in dynamic combinatorial chemistry in water. At neutral pH, diselenides are found to mix with disulfides and form dynamic combinatorial libraries of diselenides, disulfides, and selenenylsulfides. This journal is......Diselenide exchange is introduced as a reversible reaction in dynamic combinatorial chemistry in water. At neutral pH, diselenides are found to mix with disulfides and form dynamic combinatorial libraries of diselenides, disulfides, and selenenylsulfides. This journal is...

Expert system for diagnostics and status monitoring of NPP water chemistry condition

International Nuclear Information System (INIS)

Shvedova, M.N.; Kritski, V.G.; Zakharova, S.V.; Benediktov, V.B.; Nikolaev, F.V.

2002-01-01

Water chemistry condition (WCC) has been the subject of constant study and improvement up to the present day. It is connected with the presence of a direct relationship between the violation of water chemistry regulation on the one hand and components reliability of the circuit's equipment and cost-effectiveness of their operation on the other. It dictates the necessity to apply different optimization methods in the field of monitoring and use of information analytical and diagnostic systems to assess WCC quality, control and support. LI ''VNIPIET'' employees have, for several years, been developing an expert diagnostic system for supporting WCC and status monitoring of RBMK - reactor NPPs [2]. This system has not only conveniently organized the traditional functions of information acquisition and storage, a complete presentation of information in the form of tables, graphs of a dynamical changes of parameters and formation regular reports, diagnostic functions and issuing recommendations on WCC correction, but it also allows the assessment of confidence in the diagnosis made, relying on a wide range of numerical estimates, which were calculated by the use of expert data, and to make a credible prediction of an existing situation development. (authors)

Environmental and legal aspects of cooling water chemistry

International Nuclear Information System (INIS)

Hoffmann, H.J.

1988-01-01

The discharge and management of cooling water and waste water are subject to a number of ecological and legal requirements. For example, waste heat and cooling water constituents may affect surface bodies of water, or waste water discharge may have adverse effects on surface water and ground water. Waste water and cooling water discharge are subject to the Water Management Act (WHG) and the Waste Water Act, with about 50 administrative regulations. The requirements on water chemistry and analysis are gone into. (orig./HP) [de

Design Features of the SMART Water Chemistry

International Nuclear Information System (INIS)

Byung Seon Choi; Seong Hoon Kim; Juhyeon Yoon; Doo Jeong Lee; Yoon Yeong Bae; Sung Kyun Zee

2004-01-01

The design features for the primary water chemistry for the SMART are introduced from the viewpoint of the system characteristics and the chemical design concept. The most essential differences in water chemistry between the commercially operating PWRs and SMART are characterized by the presence of boron in the water and the operating mode of the purification system. SMART is a soluble boron free reactor, and the ammonia is used as a pH reagent. The material for SMART steam generator is also different from the standard material of the commercially operating PWRs: titanium alloy for the steam generator tubes. In SMART hydrogen gas which suppresses a generation of oxidizing species by the radiolysis processes in the reactors is not added to the primary coolant, but is normally generated from the radiolysis of the ammonia as the coolant passes through the core. Ammonia is added once per shift because SMART reactor has no letdown and charging system during power operation. Because of these competing processes, the concentrations of hydrogen, nitrogen and ammonia in the primary coolant are in equilibrium, which depend on the decomposition and/or combination rate of the ammonia. The level of permissible oxygen concentration in the primary coolant can be ensured by both suppression of the water radiolysis through maintaining a high enough hydrogen concentration in the primary coolant and by a restriction of the oxygen ingress into the primary coolant with the makeup water. The ammonia chemistry in SMART reactor eliminates the need for hydrogen injection for the control of the dissolved oxygen in the primary coolant because of spontaneous generation of hydrogen and nitrogen produced by the reaction of the ammonia decomposition. (authors)

PWR Secondary Water Chemistry Control Status: A Summary of Industry Initiatives, Experience and Trends Relative to the EPRI PWR Secondary Water Chemistry Guidelines

International Nuclear Information System (INIS)

Fruzzetti, Keith; Choi, Samuel

2012-09-01

The latest revision of the EPRI Pressurized Water Reactor (PWR) Secondary Water Chemistry Guidelines was issued in February 2009. The Guidelines continue to focus on minimizing stress corrosion cracking (SCC) of steam generator tubes, as well as minimizing degradation of other major components / subsystems of the secondary system. The Guidelines provide a technically-based framework for a plant-specific and effective PWR secondary water chemistry program. With the issuance of Revision 7 of the Guidelines in 2009, many plants have implemented changes that allow greater flexibility on startup. For example, the previous Guidelines (Revision 6) contained a possible low power hold at 5% power and a possible mid power hold at approximately 30% power based on chemistry constraints. Revision 7 has established a range over which a plant-specific value can be chosen for the possible low power hold (between 5% and 15%) and mid power hold (between 30% and 50%). This has provided plants the ability to establish significant plant evolutions prior to reaching the possible power hold; such as establishing seal steam to the condenser, placing feed pumps in service, or initiating forward flow of heater drains. The application of this flexibility in the industry will be explored. This paper also highlights the major initiatives and industry trends with respect to PWR secondary chemistry; and outlines the recent work to effectively address them. These will be presented in light of recent operating experience, as derived from EPRI's PWR Chemistry Monitoring and Assessment (CMA) program (which contains more than 400 cycles of operating chemistry data). (authors)

Advanced water chemistry management in power plants

International Nuclear Information System (INIS)

Regis, V.; Sigon, F.

1995-01-01

Advanced water management based on low external impact cycle chemistry technologies and processes, effective on-line water control and monitoring, has been verified to improve water utilization and to reduce plant liquid supply and discharge. Simulations have been performed to optimize system configurations and performances, with reference to a 4 x 320 MWe/once-through boiler/AVT/river cooled power plant, to assess the effectiveness of membrane separation technologies allowing waste water reuse, to enhance water management system design and to compare these solutions on a cost/benefit analysis. 6 refs., 3 figs., 3 tabs

Standard and hydrazine water chemistry in primary circuit of VVER 440 units

International Nuclear Information System (INIS)

Burclova, J.

1992-01-01

Standard ammonia-potassium-boron water chemistry of 8 units with VVER 440 in CSFR is discussed as well as the corrosion product activity in the coolant during steady state and shut-down period and surface activity, dose rate build-up and occupational radiation exposure. Available data on hydrazine application (USSR, Hungary) indicate the possibility of the radiation field decreasing. Nevertheless the detailed analysis of 55 cycles of operation under standard water chemistry in Czechoslovakia allows to expect the comparable results for both water chemistries. (author)

Water and complex organic chemistry in the cold dark cloud Barnard 5: Observations and Models

Science.gov (United States)

Wirström, Eva; Charnley, Steven B.; Taquet, Vianney; Persson, Carina M.

2015-08-01

Studies of complex organic molecule (COM) formation have traditionally been focused on hot cores in regions of massive star formation, where chemistry is driven by the elevated temperatures - evaporating ices and allowing for endothermic reactions in the gas-phase. As more sensitive instruments have become available, the types of objects known to harbour COMs like acetaldehyde (CH3CHO), dimethyl ether (CH3OCH3), methyl formate (CH3OCHO), and ketene (CH2CO) have expanded to include low mass protostars and, recently, even pre-stellar cores. We here report on the first in a new category of objects harbouring COMs: the cold dark cloud Barnard 5 where non-thermal ice desorption induce complex organic chemistry entirely unrelated to local star-formation.Methanol, which only forms efficiently on the surfaces of dust grains, provide evidence of efficient non-thermal desorption of ices in the form of prominent emission peaks offset from protostellar activity and high density tracers in cold molecular clouds. A study with Herschel targeting such methanol emission peaks resulted in the first ever detection of gas-phase water offset from protostellar activity in a dark cloud, at the so called methanol hotspot in Barnard 5.To model the effect a transient injection of ices into the gas-phase has on the chemistry of a cold, dark cloud we have included gas-grain interactions in an existing gas-phase chemical model and connected it to a chemical reaction network updated and expanded to include the formation and destruction paths of the most common COMs. Results from this model will be presented.Ground-based follow-up studies toward the methanol hotspot in B5 have resulted in the detection of a number of COMs, including CH2CO, CH3CHO, CH3OCH3, and CH3OCHO, as well as deuterated methanol (CH2DOH). Observations have also confirmed that COM emission is extended and not localised to a core structure. The implications of these observational and theoretical studies of B5 will be discussed

Automated Water Chemistry Control at University of Virginia Pools.

Science.gov (United States)

Krone, Dan

1997-01-01

Describes the technologically advanced aquatic and fitness center at the University of Virginia. Discusses the imprecise water chemistry control at the former facility and its intensive monitoring requirements. Details the new chemistry control standards initiated in the new center, which ensure constant chlorine and pH levels. (RJM)

Brunswick-2 water chemistry. Interim report

International Nuclear Information System (INIS)

Miller, A.D.

1981-04-01

This study summarizes and interprets the nearly half million data points obtained through January of 1978 from the continuous monitoring equipment and data acquisition computers at Brunswick-2. Dissolved oxygen, specific conductance, and pH levels of 12 separate sample points were measured and correlated to plant operation, leading to a more complete understanding of the water chemistry of boiling water reactors. The measured parameters were characterized for various reactor power levels, startups, shutdowns, resin intrusions, etc

Water Chemistry Control in Reducing Corrosion and Radiation Exposure at PWR Reactor

International Nuclear Information System (INIS)

Febrianto

2006-01-01

Water chemistry control plays an important role in relation to plant availability, reliability and occupational radiation exposures. Radiation exposures of nuclear plant workers are determined by the radiation rate dose and by the amount maintenance and repair work time Water chemistry has always been, from beginning of operation of power Pressurized Water Reactor, an important factor in determining the integrity of reactor components, fuel cladding integrity and minimize out of core radiation exposures. For primary system, the parameters to control the quality of water chemistry have been subject to change in time. Reactor water coolant pH need to be optimally controlled and be operated in range pH 6.9 to 7.4. At pH lower than 6.9, cause increasing the radiation exposure level and increasing coolant water pH higher than 7.4 will decrease radiation exposure level but increasing risk to fuel cladding and steam generator tube. Since beginning 90 decade, PWR water coolant pH tend to be operated at pH 7.4. This paper will discuss concerning water chemistry development in reducing corrosion and radiation exposure dose in PWR reactor. (author)

Development of High Temperature Chemistry Measurement System for Establishment of On-Line Water Chemistry Surveillance Network in Nuclear Power Plant

International Nuclear Information System (INIS)

Yeon, Jei Won; Kim, Won Ho; Song, Kyu Seok; Joo, Ki Soo; Choi, Ke Chon; Ha, Yeong Keong; Ahn, Hong Joo; Im, Hee Jung; Maeng, Wan Young

2010-07-01

An integrated high-temperature water chemistry sensor (pH, E redox ) was developed for the establishment of the on-line water chemistry surveillance system in nuclear power plants. The basic performance of the integrated sensor was confirmed in high-temperature (280 .deg. C, 150kg/m 2 ) lithium borate solutions by using the relationship between the concentration of lithium ion and pH-E redox values. Especially, the effects of various environmental factors such as temperature, pressure, and flow rate on YSZ-based pH electrode were evaluated for ensuring the accuracy of high-temperature pH measurement. And the relationships between each water chemistry factor (pH, redox potential, electrical conductivity) were induced for enhancing the credibility of water chemistry measurement. In addition, on the basis of the evaluation of a nuclear plant design company, we suggested potential installation positions of the measurement system in a nuclear power plant

Non-equilibrium chemistry and cooling in simulations of galaxy formation

NARCIS (Netherlands)

Richings, Alexander James

2015-01-01

In this thesis we used numerical simulations to explore the role that chemistry plays in galaxy formation. Simulations of galaxies often assume chemical equilibrium, where the chemical reactions between ions and molecules have reached a steady state. However, this assumption may not be valid if the

Water chemistry and endangered white-clawed Crayfish: a literature review and field study of water chemistry association in Austropotamobius pallipes

Directory of Open Access Journals (Sweden)

Haddaway N.R.

2015-01-01

Full Text Available Populations of the endangered white-clawed crayfish (Austropotamobius pallipes have rapidly declined in distribution and density in recent decades as a result of invasive crayfish, disease and habitat degradation. The species is thought to be particularly sensitive to water chemistry, and has been proposed as a bio-indicator of water quality. Here we detail the results of a systematic review of the literature regarding the chemistry of waterbodies inhabited by white-clawed crayfish, along with a wide-scale field study of the chemistry of crayfish-inhabited waterbodies in the UK. We use these data to examine potentially significant variables influencing crayfish distribution. Several variables appear to have thresholds that affect crayfish distribution; crayfish presence was associated with high dissolved oxygen, low conductivity, ammonium, sodium, and phosphate, and to a lesser extent low sulphate, nitrate, and total suspended solids. Some variables (magnesium, potassium, sodium, sulphate, nitrate, and total suspended solids may be tolerated at moderate to high concentrations in isolation (indicated by the presence of some populations in high levels of these variables, but suites of chemical conditions may act synergistically in situ and must be considered together. Recent efforts to conserve white-clawed crayfish have included relocations to Ark Sites; novel protected habitats with reduced risk of the introduction of disease, invasive crayfish and habitat degradation. We use our findings to propose the first detailed guidelines for common water chemistry variables of potential Ark Sites for the conservation of the species throughout its European range.

History of the water chemistry for the few tube test model

International Nuclear Information System (INIS)

Moss, S.A.; Simpson, J.L.

1979-09-01

The water chemistry activities carried out in support of the Few Tube Test are described. This test was conducted to provide design confirmation data for the Clinch River Breeder Reactor Project (CRBRP) steam generators. Proposed CRBRP chemistry was followed; all volatile treatment (AVT) of water was carried out with on-line monitoring capability

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.S.; Chandrasekaran, R.; Chaturvedi, S.K.; Mahesh, R.; Sudha, V.; Josephine, P.J.; 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...

Solution chemistry

Energy Technology Data Exchange (ETDEWEB)

None

1973-07-01

Research progress is reported on studies in heavy element chemistry. Topics considered are: synergistic complexes of plutonyl ion; water uptake in synergistic systems; formation constants of some uranyl BETA -diketone complexes; thermodynamic acid dissociation constants of BETA -diketones; thermodynamic formation constants of uranyl BETA -diketonates; thiocyanate complexes of some trivalent lanthanides and actinides; stability constants of actinide complexes using dinonyl naphthalenesulfonic acid extraction; TBP extraction of actinides; stability constants of complexes of Pu(III) with 5- sulfosalicycllc acid; and solvent extraction behavior of Pu( VII). (DHM)

Water chemistry: protecting the industry's investment. Making or breaking plant operations

International Nuclear Information System (INIS)

Anon.

1983-01-01

Good water chemistry is a good way to preserve the life of steam generators and other plant components. Pipe cracks in boiling-water reactors, tube pitting, denting and cracking in pressurized-water reactors are all problems that are surfacing due to poor water chemistry, i.e., the lack of water purity. Water is essential to power generation and is corrosive under the best of conditions. But to a metal system filled with water and subject to high pressure, high temperature, and impurities such as chlorides, the potential for rapid and permanent damage rises to serious proportions. In addition, radiation levels increase from corrosive products circulated through the reactor vessel

Ground water chemistry and water-rock interaction at Olkiluoto

International Nuclear Information System (INIS)

Pitkaenen, P.; Front, K.

1992-02-01

Bedrock investigations for the final repository for low- and intermediate level wastes (VLJ repository) generated at the Olkiluoto (TVO-I and TVO-II) nuclear power plant, stareted in 1980. Since 1988 the area has been investigated for the final disposal of spent nuclear fuel. In the report the geochemistry at the nuclear waste investigation site, Olkiluoto, is evaluated. The hydrogeological data are collected from boreholes drilled down to 1000-m depth into Proterozoic crystalline bedrock. The interpretation is based on groundwater chemistry and isotope data, mineralogical data, and the structure and hydrology of the bedrock, using correlation diagrams and thermodynamic calculations (PHREEQE). The hydrogeochemistry and major processes controlling the groundwater chemistry are discussed. The groundwater types are characterized by water-rock interaction but they also show features of other origins. The fresh and brackish waters are contaminated by varying amounts of young meteoric water and brackish seawater. The saline water contains residues of possibly ancient hydrothermal waters, imprints of which are occasionally seen in the rock itself. Different mixing phenomenas are indicated by the isotope contents (O-l8/H-2, H-3) and the Ca/Cl, Na/Cl, HCO 3 /Cl, SO 4 /Cl, Br/Cl, SI(calcite)/SI(dolomite) ratios. The interaction between bedrock and groundwater is reflected by the behaviour of pH, Eh, Ca, Mg, Na, K, Fe, HCO 3 and S0 4 . Dissolution and precipitation of calcite and pyrite, and aluminosilicate hydrolysis play the major role in defining the groundwater composition of the above components

Research activities at nuclear research institute in water chemistry and corrosion

International Nuclear Information System (INIS)

Kysela, Jan

2000-01-01

Research activities at Nuclear Research Institute Rez (NRI) are presented. They are based on former heavy water reactor program and now on pressurized reactors VVER types which are operated on Czech republic. There is LVR-15 research reactor operated in NRI. The reactor and its experimental facilities is utilized for water chemistry and corrosion studies. NRI services for power plants involve water chemistry optimalization, radioactivity build-up, fuel corrosion and structural materials corrosion tests. (author)

Water at surfaces with tunable surface chemistries

Science.gov (United States)

Sanders, Stephanie E.; Vanselous, Heather; Petersen, Poul B.

2018-03-01

Aqueous interfaces are ubiquitous in natural environments, spanning atmospheric, geological, oceanographic, and biological systems, as well as in technical applications, such as fuel cells and membrane filtration. Where liquid water terminates at a surface, an interfacial region is formed, which exhibits distinct properties from the bulk aqueous phase. The unique properties of water are governed by the hydrogen-bonded network. The chemical and physical properties of the surface dictate the boundary conditions of the bulk hydrogen-bonded network and thus the interfacial properties of the water and any molecules in that region. Understanding the properties of interfacial water requires systematically characterizing the structure and dynamics of interfacial water as a function of the surface chemistry. In this review, we focus on the use of experimental surface-specific spectroscopic methods to understand the properties of interfacial water as a function of surface chemistry. Investigations of the air-water interface, as well as efforts in tuning the properties of the air-water interface by adding solutes or surfactants, are briefly discussed. Buried aqueous interfaces can be accessed with careful selection of spectroscopic technique and sample configuration, further expanding the range of chemical environments that can be probed, including solid inorganic materials, polymers, and water immiscible liquids. Solid substrates can be finely tuned by functionalization with self-assembled monolayers, polymers, or biomolecules. These variables provide a platform for systematically tuning the chemical nature of the interface and examining the resulting water structure. Finally, time-resolved methods to probe the dynamics of interfacial water are briefly summarized before discussing the current status and future directions in studying the structure and dynamics of interfacial water.

Inhibition and anti-inhibition effects of positronium formation in cyclohexane and their relation to radiation chemistry

International Nuclear Information System (INIS)

Ito, Y.; Miyake, Y.; Tabata, Y.

1982-01-01

Positronium formation in cyclohexane has been studied using C 2 H 5 Br or CCl 4 as an inhibitor and C 6 F 6 as an anti-inhibitor. The results are analyzed using an empirical formula which is well established in radiation chemistry for electron scavenging reactions in cyclohexane. The reactivity parameters derived from the radiation chemistry are shown to successfully reproduce the experimental results. Very close correlation between positronium formation and radiation chemistry is evident, and the spur reaction model of positronium formation is corroborated. From a simple model of the positron spur in which only a single ion pair and a positron is assumed, it is estimated that about 75% of the spur electron combines with the positron. (author)

Primary water chemistry monitoring from the point of view of radiation build-up

International Nuclear Information System (INIS)

Horvath, G.L.; Civin, V.; Pinter, T.

1997-01-01

Basic operational principles of a computer code system calculating the primary circuit corrosion product activities based on actual measured plant chemistry data are presented. The code system consists of two parts: FeSolub.prg: calculates the characteristic iron solubilities based on actual primary water chemistry (H 3 BO 3 KOH, ... etc.) and plant load (MW) data. A developed solubility calculation method has been applied fitted to magnetite solubility data of several authors; RADTRAN.exe: calculates primary circuit water and surface corrosion product activities based on results of FeSolub.prg or planned water chemistry data up to the next shutdown. The computer code system is going to be integrated into a general primary water chemistry monitoring and surveillance system. (author). 15 refs, 4 figs, 3 tabs

New design architecture decisions on water chemistry support systems at new VVER plants

International Nuclear Information System (INIS)

Kumanina, V.E.; Yurmanova, A.V.

2010-01-01

Major goals of nuclear power plant design upgrading are reduction of cost and construction time with unconditional safety assurance. Main ways of further improvement of nuclear power plant design are as follows: review of the results of research engineering and development and of new technologies; harmonization with international codes and standards; justified liberalization of conservatism based on operating experience and use of improved design codes. Operational experience of Russian and foreign NPPs has shown that the designs of new NPPs could be improved by upgrading water chemistry support systems. Some new design solutions for water chemistry support systems are currently implemented at new WWER plants such as Bushehr, Kudankulam, Belene, Balakovo Units 5 and 6, AES-2006 project. The paper highlights the improvements of the following systems and processes: low temperature high pressure primary coolant clean-up system; primary system surface preconditioning during pre-start hot functional testing; steam generator blowdown cleanup system; secondary water chemistry; phosphate water chemistry in intermediate cooling circuits and other auxiliary systems; alternator cooling system water chemistry; steam generator cleanup and decontamination systems. (author)

Optimization of Water Chemistry to Ensure Reliable Water Reactor Fuel Performance at High Burnup and in Ageing Plant (FUWAC). Additional Information

International Nuclear Information System (INIS)

2011-10-01

This report presents the results of the Coordinated Research Project (CRP) on Optimization of Water Chemistry to Ensure Reliable Water Reactor Fuel Performance at High Burnup and in Ageing Plants (FUWAC, 2006-2009). It provides an overview of the results of the investigations into the current state of water chemistry practice and concerns in the primary circuit of water cooled power reactors including: corrosion of primary circuit materials; deposit composition and thickness on the fuel; crud induced power shift; fuel oxide growth and thickness; radioactivity buildup in the reactor coolant system (RCS). The FUWAC CRP is a follow-up to the DAWAC CRP (Data Processing Technologies and Diagnostics for Water Chemistry and Corrosion Control in Nuclear Power Plants 2001-2005). The DAWAC project improved the data processing technologies and diagnostics for water chemistry and corrosion control in nuclear power plants (NPPs). With the improved methods for controlling and monitoring water chemistry now available, it was felt that a review of the principles of water chemistry management should be undertaken in the light of new materials, more onerous operating conditions, emergent issues such as CIPS, also known as axial offset anomaly (AOA) and the ageing of operating power plant. In the framework of this CRP, water chemistry specialists from 16 nuclear utilities and research organizations, representing 15 countries, exchanged experimental and operational data, models and insights into water chemistry management. This CD-ROM attached to the printed IAEA-TECDOC includes the report itself, detailed progress reports of three Research Coordination Meetings (RCMs) (Annexes I-III) and the reports and presentations made during the project by the participants.

Primary water chemistry control at units of Paks Nuclear Power Plant

International Nuclear Information System (INIS)

Schunk, J.; Patek, G.; Pinter, T.; Tilky, P.; Doma, A.; Osz, J.

2010-01-01

The primary water chemistry of the four identical units of Paks Nuclear Power Plant has been developed based on Western-type PWR units, taking into consideration some Soviet-Russian modifications. The political changes in 90s have also influenced the water chemistry specifications and directions. At PWR units the transition operational modes have been developed while in case of VVER units - in lack of central uniform regulation - this question has become the competence and responsibility of each individual plant. This problem has resulted in separate water chemistry developments with a considerable time delay. The needs for life-time extensions all over the World have made the development of start-up and shut-down chemistry procedures extremely important, since they considerably influence the long term and safe operation of plants. The uniformly structured limit value system, the principles applied for the system development, and the logic schemes for actions to be taken are discussed in the paper, both for normal operation and transition modes. (author)

Primary Water Chemistry Control at Units of Paks Nuclear Power Plant

Energy Technology Data Exchange (ETDEWEB)

Schunk, J.; Pinter, G. Patek T.; Tilky, P.; Doma, A. [Paks Nuclear Power Plant Co. Ltd., Paks (Hungary); Osz, J. [Budapest University of Technology and Economics, Budapest (Hungary)

2013-03-15

The primary water chemistry of the four identical units of Paks Nuclear Power Plant has been developed based on Western type PWR units, taking into consideration some Russian modifications. The political changes in the 1990s have also influenced the water chemistry specifications and directions. At PWR units the transition operational modes have been developed while in case of WWER units - in lack of central uniform regulation - this question has become the competence and responsibility of each individual plant. This problem has resulted in separate water chemistry developments with a considerable time delay. The need for lifetime extensions worldwide has made the development of startup and shutdown chemistry procedures extremely important, since they considerably influence the long term and safe operation of plants. The uniformly structured limit value system, the principles applied for the system development, and the logic schemes for actions to be taken are discussed in the paper, both for normal operation and transition modes. (author)

VVER operational experience - effect of preconditioning and primary water chemistry on radioactivity build-up

International Nuclear Information System (INIS)

Zmitko, M.; Kysela, J.; Dudjakova, K.; Martykan, M.; Janesik, J.; Hanus, V.; Marcinsky, P.

2004-01-01

The primary coolant technology approaches currently used in VVER units are reviewed and compared with those used in PWR units. Standard and modified water chemistries differing in boron-potassium control are discussed. Preparation of the VVER Primary Water Chemistry Guidelines in the Czech Republic is noted. Operational experience of some VVER units, operated in the Czech Republic and Slovakia, in the field of the primary water chemistry, and radioactivity transport and build-up are presented. In Mochovce and Temelin units, a surface preconditioning (passivation) procedure has been applied during hot functional tests. The main principles of the controlled primary water chemistry applied during the hot functional tests are reviewed and importance of the water chemistry, technological and other relevant parameters is stressed regarding to the quality of the passive layer formed on the primary system surfaces. The first operational experience obtained in the course of beginning of these units operation is presented mainly with respect to the corrosion products coolant and surface activities. Effect of the initial passivation performed during hot functional tests and the primary water chemistry on corrosion products radioactivity level and radiation situation is discussed. (author)

Predicted effect of power uprating on the water chemistry of commercial boiling water reactors

International Nuclear Information System (INIS)

Yeh, Tsung-Kuang; Wang, Mei-Ya; Chu, Charles F.; Chang Ching

2009-01-01

The approach of power uprating has been adopted by operators of light water reactors in the past few decades in order to increase the power generation efficiency of nuclear reactors. The power uprate strategy is apparently applicable to the three nuclear reactors in Taiwan as well. When choosing among the three types of power uprating, measurement uncertainty, stretch power uprating, and extended power uprating, a deliberate and thorough evaluation is required before a final decision and an optimal selection can be made. One practical way of increasing the reactor power is to deliberately adjust the fuel loading pattern and the control rod pattern and thus to avoid replacing the primary coolant pump with a new one of larger capacity. The power density of the reactor will increase with increasing power, but the mass flow rate in the primary coolant circuit (PCC) of a light water reactor will slightly increase (usually by less than 5 %) or even remain unchanged. Accordingly, an uprated power would induce higher neutron and gamma photon dose rates in the reactor coolant but have a minor or no effect on the mass flow rate of the primary coolant. The radiolysis product concentrations and the electrochemical corrosion potential (ECP) values differ largely in the PCC of a boiling water reactor (BWR). It is very difficult to measure the water chemistry data directly at various locations of an actual reactor. Thus the impact of power uprating on the water chemistry of a BWR operating under hydrogen water chemistry (HWC) can only be theoretically evaluated through computer modelling. In this study, the DEMACE computer code was modified to investigate the impact of power uprating on the water chemistry under a fixed mass flow rate in the primary coolant circuit of a BWR/6 type plant. Simulations were carried out for hydrogen concentrations in feedwater ranging from 0.0 to 2.0 mg . kg -1 and for power levels ranging from 100 % to 120 %. The responses of water chemistry and ECP

Groundwater fluxes into a submerged sinkhole area, Central Italy, using radon and water chemistry

Energy Technology Data Exchange (ETDEWEB)

Tuccimei, P. [Dipartimento di Scienze Geologiche, Universita ' Roma Tre' , Largo San Leonardo Murialdo 1, 00146 Rome (Italy)]. E-mail: tuccimei@uniroma3.it; Salvati, R. [Dipartimento di Scienze Geologiche, Universita ' Roma Tre' , Largo San Leonardo Murialdo 1, 00146 Rome (Italy); Capelli, G. [Dipartimento di Scienze Geologiche, Universita ' Roma Tre' , Largo San Leonardo Murialdo 1, 00146 Rome (Italy); Delitala, M.C. [Dipartimento di Scienze Geologiche, Universita ' Roma Tre' , Largo San Leonardo Murialdo 1, 00146 Rome (Italy); Primavera, P. [Dipartimento di Scienze Geologiche, Universita ' Roma Tre' , Largo San Leonardo Murialdo 1, 00146 Rome (Italy)

2005-10-15

The groundwater contribution into Green Lake and Black Lake (Vescovo Lakes Group), two cover collapse sinkholes in Pontina Plain (Central Italy), was estimated using water chemistry and a {sup 222}Rn budget. These data can constrain the interactions between sinkholes and deep seated fluid circulation, with a special focus on the possibility of the bedrock karst aquifer feeding the lake. The Rn budget accounted for all quantifiable surface and subsurface input and output fluxes including the flux across the sediment-water interface. The total value of groundwater discharge into Green Lake and Black Lake ({approx}540 {+-} 160 L s{sup -1}) obtained from the Rn budget is lower than, but comparable with historical data on the springs group discharge estimated in the same period of the year (800 {+-} 90 L s{sup -1}). Besides being an indirect test for the reliability of the Rn-budget 'tool', it confirms that both Green and Black Lake are effectively springs and not simply 'water filled' sinkholes. New data on the water chemistry and the groundwater fluxes into the sinkhole area of Vescovo Lakes allows the assessment of the mechanism responsible for sinkhole formation in Pontina Plain and suggests the necessity of monitoring the changes of physical and chemical parameters of groundwater below the plain in order to mitigate the associated risk.

Groundwater fluxes into a submerged sinkhole area, Central Italy, using radon and water chemistry

International Nuclear Information System (INIS)

Tuccimei, P.; Salvati, R.; Capelli, G.; Delitala, M.C.; Primavera, P.

2005-01-01

The groundwater contribution into Green Lake and Black Lake (Vescovo Lakes Group), two cover collapse sinkholes in Pontina Plain (Central Italy), was estimated using water chemistry and a 222 Rn budget. These data can constrain the interactions between sinkholes and deep seated fluid circulation, with a special focus on the possibility of the bedrock karst aquifer feeding the lake. The Rn budget accounted for all quantifiable surface and subsurface input and output fluxes including the flux across the sediment-water interface. The total value of groundwater discharge into Green Lake and Black Lake (∼540 ± 160 L s -1 ) obtained from the Rn budget is lower than, but comparable with historical data on the springs group discharge estimated in the same period of the year (800 ± 90 L s -1 ). Besides being an indirect test for the reliability of the Rn-budget 'tool', it confirms that both Green and Black Lake are effectively springs and not simply 'water filled' sinkholes. New data on the water chemistry and the groundwater fluxes into the sinkhole area of Vescovo Lakes allows the assessment of the mechanism responsible for sinkhole formation in Pontina Plain and suggests the necessity of monitoring the changes of physical and chemical parameters of groundwater below the plain in order to mitigate the associated risk

Primary water chemistry monitoring from the point of view of radiation build-up

Energy Technology Data Exchange (ETDEWEB)

Horvath, G L [Institute for Electrical Power Research, Budapest (Hungary); Civin, V [Hungarian Electricity Generating Board, Budapest (Hungary); Pinter, T [Nuclear Power Plant PAKS, Budapest (Hungary)

1997-02-01

Basic operational principles of a computer code system calculating the primary circuit corrosion product activities based on actual measured plant chemistry data are presented. The code system consists of two parts: FeSolub.prg: calculates the characteristic iron solubilities based on actual primary water chemistry (H{sub 3}BO{sub 3}KOH, ... etc.) and plant load (MW) data. A developed solubility calculation method has been applied fitted to magnetite solubility data of several authors; RADTRAN.exe: calculates primary circuit water and surface corrosion product activities based on results of FeSolub.prg or planned water chemistry data up to the next shutdown. The computer code system is going to be integrated into a general primary water chemistry monitoring and surveillance system. (author). 15 refs, 4 figs, 3 tabs.

Water chemistry of Atucha II PHWVR. Design concepts and evolution

International Nuclear Information System (INIS)

Chocron, Mauricio; Rodriguez, Ivanna; Duca, Jorge; Fernandez, Ricardo; Rico, Jorge

2007-01-01

Full text: Atucha II is a pressurized heavy water vessel reactor designed by Siemens-KWU, currently part of AREVA NP, of 745 MWe and similar to Atucha I, which has been in operation over 25 years. The primary heat transport system (PHTS) is composed by vertical channels (277-313 C degrees) that allocate the fuel elements while the moderator circuit is composed by a partially separated circuit (142-173 C degrees). The moderation power is transferred to the feedwater through the moderator heat exchangers (HX). These HXs operate as the last, high pressure water-steam cycle heaters as well. Materials (with exception of fuel channels and fuel sheaths which are made of zirconium alloys) are all austenitic steels while cobalt containing alloys have been all replaced at the design stage. Steam generator and moderator HX tubing are Alloy 800 made. The core is operated without boron except with the first fresh nucleus. The secondary circuit or Balance of plant (BOP) is similar in conception to that of a PWR but the moderator HXs. It is entirely built of ferrous alloys, has a feedwater-deaerator tank and moisture separator. The energy sink is the Rio de la Plata River. The Reactors Chemistry Department, Chemistry Division, National Atomic Energy Commission, in its character of R and D institution has been committed by CNA II-N.A.S.A Project to prepare the water chemistry specifications, water chemistry engineering and manuals, considering the type of reactor, design and construction aspects and operation characteristics, taking into account the current state-of-the art and worldwide standards. This includes conceptual aspects and implementation and operative aspects as well. This documentation will be released after a designer's review as it has been stated in the respective agreement. Respecting the confidentiality agreement between CNEA and NASA and the confidentiality regarding handling original documentation provided by the designer, it is considered illustrative to

Variation of the effectiveness of hydrogen water chemistry in a boiling water reactor during power coastdown operations

International Nuclear Information System (INIS)

Yeh Tsungkuang; Wang Meiya; Chu, Charles F.; Chang Ching

2009-01-01

A theoretical model was adapted to evaluate the impact of power coastdown on the water chemistry of a commercial boiling water reactor (BWR) in this work. In principle, the power density of a nuclear reactor upon a power level decrease would immediately be lowered, followed by water chemistry variations due to reduced radiolysis of water and extended coolant residence times in the core and near-core regions. It is currently a common practice for a commercial BWR to adopt hydrogen water chemistry (HWC) for corrosion mitigation. The optimal feedwater hydrogen concentration may be different after a power coastdown is implemented in a BWR. A computer code DEMACE was used in the current study to investigate the impact of various power coastdown levels on major radiolytic species concentrations and electrochemical corrosion potential (ECP) behavior of components in the primary coolant circuit of a domestic reactor operating under either normal water chemistry or HWC. Our analyses indicated that under a rated core flow rate the chemical species concentrations and the ECP did not vary monotonously with decreases in reactor power level at a fixed feedwater hydrogen concentration. In particular, ECP variations basically followed the patterns of hydrogen peroxide in the select regions and exhibited high values at power level of 90% for Reactor X. (author)

The Influence of Geology and Other Environmental Factors on Stream Water Chemistry and Benthic Invertebrate Assemblages

OpenAIRE

Olson, John R.

2012-01-01

Catchment geology is known to influence water chemistry, which can significantly affect both species composition and ecosystem processes in streams. However, current predictions of how stream water chemistry varies with geology are limited in both scope and precision, and we have not adequately tested the specific mechanisms by which water chemistry influences stream biota. My dissertation research goals were to (1) develop empirical models to predict natural base-flow water chemistry from ca...

Effect of Water Chemistry Variations on Corrosion of Zr-Alloys for BWR Applications

International Nuclear Information System (INIS)

Kim, Young-Jin; Yang- Lin, Pi; Lutz, Dan; Kucuk, Aylin; Cheng, Bo

2012-09-01

Two reference water chemistry conditions (60 ppb Zn and 60 μg/cm 2 Pt/Rh with either 500 ppb O 2 and 500 ppb H 2 O 2 , or 150 ppb H 2 ) were chosen for testing at 300 deg. C in refreshed autoclaves. For each reference water chemistry, the potential effects due to three chemical impurities of interest to BWRs (33 ppm Na, 10 ppm Li, and 10 ppm EHC fluid) were evaluated. Zircaloy-2 and GNF-Ziron (a Zr-based alloy with higher Fe additions than Zircaloy-2) cladding tubes were tested and the effects of tubing process variation and pre-filming were investigated. Tested channel materials included Zircaloy-2, Zircaloy-4, GNF-Ziron and NSF (a Zr-based alloy with Sn, Nb and Fe additions). The corrosion weight gain and hydrogen absorption were measured up to 12 months of exposure for a given water chemistry condition. Tests under 150 ppb H 2 based water chemistry, with or without chemical impurities, generally resulted in greater amounts of corrosion after 12 month exposure compared with 500 ppb O 2 and 500 ppb H 2 O 2 based water chemistries. Of the added chemical impurities, only 33 ppm Na addition produced slightly increased corrosion. Under various test conditions, the presence of a thin pre-film resulted in some initial corrosion benefits, but the benefits were no longer evident after 12 months exposure; however, slight hydrogen benefits remained. For GNF-Ziron cladding, hydrogen absorption was generally lower compared with similarly processed Zircaloy-2 under 150 ppb H 2 based water chemistry, when corrosion was generally higher. Of the channel material tested, NSF developed the lowest level of hydrogen absorption, particularly under 150 ppb H 2 based water chemistries. (authors)

The Role of Water Chemistry in Marine Aquarium Design: A Model System for a General Chemistry Class

Science.gov (United States)

Keaffaber, Jeffrey J.; Palma, Ramiro; Williams, Kathryn R.

2008-01-01

Water chemistry is central to aquarium design, and it provides many potential applications for discussion in undergraduate chemistry and engineering courses. Marine aquaria and their life support systems feature many chemical processes. A life support system consists of the entire recirculation system, as well as the habitat tank and all ancillary…

Student Perceptions of Online Homework Use for Formative Assessment of Learning in Organic Chemistry

Science.gov (United States)

Richards-Babb, Michelle; Curtis, Reagan; Georgieva, Zornitsa; Penn, John H.

2015-01-01

Use of online homework as a formative assessment tool for organic chemistry coursework was examined. Student perceptions of online homework in terms of (i) its ranking relative to other course aspects, (ii) their learning of organic chemistry, and (iii) whether it improved their study habits and how students used it as a learning tool were…

Medium pressure boiler water chemistry optimization using neutralizing amines mixture reagent AMINAT™ PK-2 at CEPP “Borovichi Refractories Plant” of JSC “BKO”

Science.gov (United States)

Guseva, O. V.; Butakova, M. V.; Orlov, K. A.; Vinogradov, S. V.; Pavlenko, L. S.

2017-11-01

An overview of the neutralizing amine based reagent AMINAT PK-2 usage for water chemistry of steam boilers for medium pressure boiler was given. Long term experiment showed that new reagent allows to decrease corrosion rate comparing with old water chemistry based on ammonia only. Two dosage schemes in different cycle places discussed. Scheme with two points on injection showed better results. Results of corrosion rates experiments and photos of tubes inner surfaces are presented. Based on fuel savings due to reducing scale formation the total annual economy for last year was 5.1 million Russian roubles.

A preliminary analysis of water chemistry of the Mkuze Wetland ...

African Journals Online (AJOL)

In order to investigate the water chemistry of this system, water samples were collected throughout the study area from surface water, groundwater, pan and reed swamp sites, as well as a rainwater sample. These were analysed for chloride, sodium, potassium, calcium, magnesium, iron and silicon. Four main water bodies ...

Operating experience in correcting severe secondary chemistry upsets by controlling makeup water organics (TOC)

International Nuclear Information System (INIS)

Flint, W.G.; Mc Intosh, R.J.

1986-01-01

In this paper following observations are presented: conductivity and chloride excursions in steam condensate were directly linked to makeup water quality. Data strongly suggests that the breakdown of makeup water organics was responsible for substandard condensate water quality; although the short-term effects of gross organic contamination have been documented, the longer term consequences of continuous exposure by moderate organic levels needs to be addressed; a greater understanding of the organic removal efficiency of the various water purification technologies is essential to controlling TOC contamination; and a much better understanding of makeup plant chemistry and the interrelationship of makeup water contamination and plant chemistry has proven essential to optimizing plant performance and guaranteeing the best possible steam chemistry. The role of the chemistry group as an active participant in operations has been proven at Kewaunee Nuclear Plant

High Energy Radical Chemistry Formation of HCN- rich Atmospheres on early Earth

Czech Academy of Sciences Publication Activity Database

Ferus, Martin; Kubelík, Petr; Knížek, Antonín; Pastorek, Adam; Sutherland, J.D.; Civiš, Svatopluk

2017-01-01

Roč. 7, č. 1 (2017), č. článku 6275. ISSN 2045-2322 R&D Projects: GA ČR GA17-05076S; GA MŠk(CZ) LM2015083; GA MŠk LG15013 Grant - others:Akademie věd - GA AV ČR(CZ) R200401521 Institutional support: RVO:61388955 Keywords : high-power laser * transform emission-spectroscopy * induced dielectric-breakdown * prebiotic organic-synthesis * nucleobase formation Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 4.259, year: 2016

Experience on KKNPP VVER 1000 MWe water chemistry

International Nuclear Information System (INIS)

Ganesh, S.; Selvaraj, S.; Balasubramanian, M.R.; Selvavinayagam, P.; Pillai, Suresh Kumar

2015-01-01

Kudankulam Nuclear Power Project consists of pressurized water reactor (VVER) 2 x 1000 MWe constructed in collaboration with Russian Federation at Kudankulam in Tirunelveli District, Tamilnadu. Unit - 1 attained criticality on July 13 th 2013 and the unit was synchronized to grid on 22 nd October 2013. This paper highlights experience gained on water chemistry regime for primary and secondary circuit. (author)

Classifying hot water chemistry: Application of MULTIVARIATE STATISTICS

OpenAIRE

Sumintadireja, Prihadi; Irawan, Dasapta Erwin; Rezky, Yuanno; Gio, Prana Ugiana; Agustin, Anggita

2016-01-01

This file is the dataset for the following paper "Classifying hot water chemistry: Application of MULTIVARIATE STATISTICS". Authors: Prihadi Sumintadireja1, Dasapta Erwin Irawan1, Yuano Rezky2, Prana Ugiana Gio3, Anggita Agustin1

A physico-chemical characterisation technique for determining the pore-water chemistry in argillaceous rocks

International Nuclear Information System (INIS)

Baeyens, B.; Bradbury, M.H.

1991-09-01

A prerequisite for carrying out credible sorption studies is the definition of an aqueous phase composition which is in equilibrium with the solid phase. Experimental methods and data analysis procedures are described which enable an equilibrium water composition to be produced for argillaceous rocks which is not dependent on liquid to solid (L:S) ratios. Since a Valanginian marl formation is under consideration by Nagra as a potential rock for the disposal of low and short-lived medium level radioactive waste in Switzerland, samples of this material were chosen for this investigation. Aqueous phase and nickel ethylenediamine extraction experiments were carried out at different L:S ratios under controlled atmosphere conditions (P CO 2 =10 -2 bar, O 2 ≤ 5 ppm ). The results from these tests and petrographical examinations were combined to define the system in terms of the physico-chemical characteristics of the clay mineral component (CEC and cation occupancies) and the identities of highly soluble and solubility limited phases in the marl. The geochemical code PHREEQE was used in conjunction with the Gapon equations to calculate the pore water composition. This work clearly showed that pore water chemistries obtained from aqueous extracts alone may lead to an arbitrary water chemistry in argillaceous rock systems, particularly with respect to ionic composition and ionic strength, which may have important consequences for radionuclide speciation and sorption studies. (author) 11 figs., 12 tabs., 25 refs

Hot functional test chemistry - long term experience

International Nuclear Information System (INIS)

Vonkova, K.; Kysela, J.; Marcinsky, M.; Martykan, M.

2010-01-01

Primary circuit materials undergo general corrosion in high temperature, deoxygenated, neutral or mildly alkaline solutions to form thin oxide films. These oxide layers (films) serve as protective film and mitigate the further corrosion of primary materials. Inner chromium-rich oxide layer has low cation diffusion coefficients and thus control iron and nickel transport from the metal surface to the outer layer and their dissolution into the coolant. Much less corrosion products are generated by the compact, integral and stable oxide (passivation) layer. For the latest Czech and Slovak stations commissioned (Temelin and Mochovce) a modified Hot Functional Test (HFT) chemistry was developed in the NRI Rez. Chromium rich surface layer formatted due to modified HTF chemistry ensures lower corrosion rates and radiation field formation and thus also mitigates crud formation during operation. This procedure was also designed to prepare the commissioned unit for the further proper water chemistry practise. Mochovce 1 (SK) was the first station commissioned using these recommendations in 1998. Mochovce 2 (1999) and Temelin 1 and 2 (CZ - 2000 and 2002) were subsequently commissioned using these guidelines too. The main principles of the controlled primary water chemistry applied during the hot functional tests are reviewed and importance of the water chemistry, technological and other relevant parameters is stressed regarding to the quality of the passive layer formed on the primary system surfaces. Samples from Mochovce indicated that duplex oxide layers up to 20 μm thick were produced, which were mainly magnetite substituted with nickel and chromium (e.g. 60-65% Fe, 18-28% Cr, 9-12% Ni, <1% Mn and 1-2% Si on a stainless steel primary circuit sample). Long term operation experience from both nuclear power plants are discussed in this paper. Radiation field, occupational radiation exposure and corrosion layers evolution during the first c. ten years of operation are

Role of photoexcited nitrogen dioxide chemistry on ozone formation and emission control strategy over the Pearl River Delta, China

Science.gov (United States)

A new hydroxyl radical formation pathway via photo-excited nitrogen dioxide chemistry is incorporated into a chemistry-only box model as well as a 3D air quality model to examine its potential role on ozone formation and emission control strategy over the Pearl River Delta region...

Design, Implementation, and Evaluation of a Flipped Format General Chemistry Course

Science.gov (United States)

Weaver, Gabriela C.; SturtevantHannah G.

2015-01-01

Research has consistently shown that active problem-solving in a collaborative environment supports more effective learning than the traditional lecture approach. In this study, a flipped classroom format was implemented and evaluated in the chemistry majors' sequence at Purdue University over a period of three years. What was formerly lecture…

Managing the water chemistry of a CANDU reactor with an expert system

International Nuclear Information System (INIS)

Lamirande, S.; Roberge, P.R.

1990-01-01

The aim of this project was to capture the expertise of Ontario Hydro in the water chemistry of the heat transport system (HTS) of the CANDU nuclear reactor and transform it into an Expert System prototype. The end product is an Expert System which can realistically diagnose situations and recommend proper courses of action based on the user's water chemistry analysis

Irradiation capability of Japanese materials test reactor for water chemistry experiments

International Nuclear Information System (INIS)

Hanawa, Satoshi; Hata, Kuniki; Chimi, Yasuhiro; Nishiyama, Yutaka; Nakamura, Takehiko

2012-09-01

Appropriate understanding of water chemistry in the core of LWRs is essential as chemical species generated due to water radiolysis by neutron and gamma-ray irradiation govern corrosive environment of structural materials in the core and its periphery, causing material degradation such as stress corrosion cracking. Theoretical model calculation such as water radiolysis calculation gives comprehensive understanding of water chemistry at irradiation field where we cannot directly monitor. For enhancement of the technology, accuracy verification of theoretical models under wide range of irradiation conditions, i.e. dose rate, temperature etc., with well quantified in-pile measurement data is essential. Japan Atomic Energy Agency (JAEA) has decided to launch water chemistry experiments for obtaining data that applicable to model verification as well as model benchmarking, by using an in-pile loop which will be installed in the Japan Materials Testing Reactor (JMTR). In order to clarify the irradiation capability of the JMTR for water chemistry experiments, preliminary investigations by water radiolysis / ECP model calculations were performed. One of the important irradiation conditions for the experiments, i.e. dose rate by neutron and gamma-ray, can be controlled by selecting irradiation position in the core. In this preliminary study, several representative irradiation positions that cover from highest to low absorption dose rate were chosen and absorption dose rate at the irradiation positions were evaluated by MCNP calculations. As a result of the calculations, it became clear that the JMTR could provide the irradiation conditions close to the BWR. The calculated absorption dose rate at each irradiation position was provided to water radiolysis calculations. The radiolysis calculations were performed under various conditions by changing absorption dose rate, water chemistry of feeding water etc. parametrically. Qualitatively, the concentration of H 2 O 2 , O 2 and

Chemistry in production of heavy water and industrial solvents

International Nuclear Information System (INIS)

Thomas, P.G.

2015-01-01

Industries are the temples of modern science built on the robust foundation of science and technology. The genesis of giant chemical industries is from small laboratories where the scientific thoughts are fused and transformed into innovative technologies Heavy water production is an energy intensive giant chemical industry where various hazardous and flammable chemicals are handled, extreme operating conditions are maintained and various complex chemical reactions are involved. Chemistry is the back bone to all chemical industrial activities and plays a lead role in heavy water production also. Heavy Water Board has now mastered the technology of design, construction, operation and maintenance of Heavy Water plants as well as fine tuning of the process make it more cost effective and environment friendly. Heavy Water Board has ventured into diversified activities intimately connected with our three stages of Nuclear Power Programme. Process development for the production of nuclear grade solvents for the front end and back end of our nuclear fuel cycle is one area where we have made significant contributions. Heavy Water Board has validated, modified and fine-tuned the synthesis routes for TBP, D2EHPA, TOPO, TAPO TIAP, DNPPA, D2EHPA-II, DHOA etc and these solvents were accepted by end users. Exclusive campaigns were carried out in laboratory scale, bench scale and pilot plant scale before scaling up to industrial scale. The process chemistry is understood very well and chemical parameters were monitored in every step of the synthesis. It is a continual improvement cycle where fine tuning is carried out for best quality and yield of product at lowest cost. In this presentation, an attempt is made to highlight the role of chemistry in the production of Heavy Water and industrial solvents

Influence of climate on alpine stream chemistry and water sources

Science.gov (United States)

Foks, Sydney; Stets, Edward; Singha, Kamini; Clow, David W.

2018-01-01

The resilience of alpine/subalpine watersheds may be viewed as the resistance of streamflow or stream chemistry to change under varying climatic conditions, which is governed by the relative size (volume) and transit time of surface and subsurface water sources. Here, we use end‐member mixing analysis in Andrews Creek, an alpine stream in Rocky Mountain National Park, Colorado, from water year 1994 to 2015, to explore how the partitioning of water sources and associated hydrologic resilience change in response to climate. Our results indicate that four water sources are significant contributors to Andrews Creek, including snow, rain, soil water, and talus groundwater. Seasonal patterns in source‐water contributions reflected the seasonal hydrologic cycle, which is driven by the accumulation and melting of seasonal snowpack. Flushing of soil water had a large effect on stream chemistry during spring snowmelt, despite making only a small contribution to streamflow volume. Snow had a large influence on stream chemistry as well, contributing large amounts of water with low concentrations of weathering products. Interannual patterns in end‐member contributions reflected responses to drought and wet periods. Moderate and significant correlations exist between annual end‐member contributions and regional‐scale climate indices (the Palmer Drought Severity Index, the Palmer Hydrologic Drought Index, and the Modified Palmer Drought Severity Index). From water year 1994 to 2015, the percent contribution from the talus‐groundwater end member to Andrews Creek increased an average of 0.5% per year (p < 0.0001), whereas the percent contributions from snow plus rain decreased by a similar amount (p = 0.001). Our results show how water and solute sources in alpine environments shift in response to climate variability and highlight the role of talus groundwater and soil water in providing hydrologic resilience to the system.

An evaluation of water quality in private drinking water wells near natural gas extraction sites in the Barnett Shale formation.

Science.gov (United States)

Fontenot, Brian E; Hunt, Laura R; Hildenbrand, Zacariah L; Carlton, Doug D; Oka, Hyppolite; Walton, Jayme L; Hopkins, Dan; Osorio, Alexandra; Bjorndal, Bryan; Hu, Qinhong H; Schug, Kevin A

2013-09-03

Natural gas has become a leading source of alternative energy with the advent of techniques to economically extract gas reserves from deep shale formations. Here, we present an assessment of private well water quality in aquifers overlying the Barnett Shale formation of North Texas. We evaluated samples from 100 private drinking water wells using analytical chemistry techniques. Analyses revealed that arsenic, selenium, strontium and total dissolved solids (TDS) exceeded the Environmental Protection Agency's Drinking Water Maximum Contaminant Limit (MCL) in some samples from private water wells located within 3 km of active natural gas wells. Lower levels of arsenic, selenium, strontium, and barium were detected at reference sites outside the Barnett Shale region as well as sites within the Barnett Shale region located more than 3 km from active natural gas wells. Methanol and ethanol were also detected in 29% of samples. Samples exceeding MCL levels were randomly distributed within areas of active natural gas extraction, and the spatial patterns in our data suggest that elevated constituent levels could be due to a variety of factors including mobilization of natural constituents, hydrogeochemical changes from lowering of the water table, or industrial accidents such as faulty gas well casings.

Formation and Dimerization of NO2 A General Chemistry Experiment

Science.gov (United States)

Hennis, April D.; Highberger, C. Scott; Schreiner, Serge

1997-11-01

We have developed a general chemistry experiment which illustrates Gay-Lussac's law of combining volumes. Students are able to determine the partial pressures and equilibrium constant for the formation and dimerization of NO2. The experiment can be carried out in about 45 minutes with students working in groups of two. The experiment readily provides students with data that can be manipulated with a common spreadsheet.

Nitrate pollution and surface water chemistry in Shimabara, Nagasaki Prefecture, Japan

Science.gov (United States)

Nakagawa, K.; Amano, H.

2017-12-01

Shimabara city has been experiencing serious nitrate pollution in groundwater. To evaluate nitrate pollution and water chemistry in surface water, water samples were collected at 42 sampling points in 15 rivers in Shimabara including a part of Unzen city from January to February 2017. Firstly, spatial distribution of water chemistry was assessed by describing stiff and piper-trilinear diagrams using major ions concentrations. Most of the samples showed Ca-HCO3 or Ca-(NO3+SO4) water types. It corresponds to groundwater chemistry. Some samples were classified into characteristic water types such as Na-Cl, (Na+K)-HCO3, and Ca-Cl. These results indicate sea water mixing and anthropogenic pollution. At the upstream of Nishi-river, although water chemistry showed Ca-HCO3, ions concentrations were higher than that of the other rivers. It indicates that this site was affected by the peripheral anthropogenic activities. Secondly, nitrate-pollution assessment was performed by using NO3-, NO2-, coprostanol (5β(H)-Cholestan-3β-ol), and cholestanol (5α(H)-Cholestan-3β-ol). NO2-N was detected at the 2 sampling points and exceeded drinking standard 0.9 mg L-1 for bottle-fed infants (WHO, 2011). NO3-N + NO2-N concentrations exceeded Japanese drinking standard 10 mg L-1 at 18 sampling points. The highest concentration was 27.5 mg L-1. Higher NO3-N levels were observed in the rivers in the northern parts of the study area. Coprostanol has been used as a fecal contamination indicator, since it can be found in only feces of higher animals. Coprostanol concentrations at 8 sampling points exceeded 700 ng L-1 (Australian drinking water standard). Coprostanol has a potential to distinguish the nitrate pollution sources between chemical fertilizer or livestock wastes, since water samples with similar NO3-N + NO2-N concentration showed distinct coprostanol concentration. The sterols ratio (5β/ (5β+5α)) exceeded 0.5 at 18 sampling points. This reveals that fecal pollution has occurred.

Water chemistry controlled aggregation and photo-transformation of silver nanoparticles in environmental waters.

Science.gov (United States)

Yin, Yongguang; Yang, Xiaoya; Zhou, Xiaoxia; Wang, Weidong; Yu, Sujuan; Liu, Jingfu; Jiang, Guibin

2015-08-01

The inevitable release of engineered silver nanoparticles (AgNPs) into aquatic environments has drawn great concerns about its environmental toxicity and safety. Although aggregation and transformation play crucial roles in the transport and toxicity of AgNPs, how the water chemistry of environmental waters influences the aggregation and transformation of engineered AgNPs is still not well understood. In this study, the aggregation of polyvinylpyrrolidone (PVP) coated AgNPs was investigated in eight typical environmental water samples (with different ionic strengths, hardness, and dissolved organic matter (DOM) concentrations) by using UV-visible spectroscopy and dynamic light scattering. Raman spectroscopy was applied to probe the interaction of DOM with the surface of AgNPs. Further, the photo-transformation and morphology changes of AgNPs in environmental waters were studied by UV-visible spectroscopy, inductively coupled plasma mass spectrometry, and transmission electron microscopy. The results suggested that both electrolytes (especially Ca(2+) and Mg(2+)) and DOM in the surface waters are key parameters for AgNP aggregation, and sunlight could accelerate the morphology change, aggregation, and further sedimentation of AgNPs. This water chemistry controlled aggregation and photo-transformation should have significant environmental impacts on the transport and toxicity of AgNPs in the aquatic environments. Copyright © 2015. Published by Elsevier B.V.

Operational experience, evolution and developments in water chemistry in Indian Nuclear Power Plants - an overview

International Nuclear Information System (INIS)

Prasad, Y.S.R.

2000-01-01

Lessons learnt from the experiences at nuclear power plants have enriched the understanding of corrosion behaviour in water systems. The need for proper water chemistry control not only during operation but also during fabrication and preoperational tests is clearly seen. It should not be construed that maintenance of proper water chemistry is a panacea for all corrosion and other associated problems. Unless adequate care is taken in selection of material and sound design and fabrication practices are followed, no regime of water chemistry can help in eliminating failure due to corrosion

Bottled water, spas, and early years of water chemistry

Science.gov (United States)

Back, William; Landa, Edward R.; Meeks, Lisa

1995-01-01

Although hot springs have been used and enjoyed for thousands of years, it was not until the late 1700s that they changed the course of world civilization by being the motivation for development of the science of chemistry. The pioneers of chemistry such as Priestley, Cavendish, Lavoisier, and Henry were working to identify and generate gases, in part, to determine their role in carbonated beverages. In the 18th century, spas in America were developed to follow the traditional activities of popular European spas. However, they were to become a dominant political and economic force in American history on three major points: (1) By far the most important was to provide a place for the leaders of individual colonies to meet and discuss the need for separation from England and the necessity for the Revolutionary War; (2) the westward expansion of the United States was facilitated by the presence of hot springs in many locations that provided the economic justification for railroads and settlement; and (3) the desire for the preservation of hot springs led to the establishment of the National Park Service. Although mineral springs have maintained their therapeutic credibility in many parts of the world, they have not done so in the United States. We suggest that the American decline was prompted by: (1) the establishment of The Johns Hopkins School of Medicine in 1893; (2) enactment of the Pure Food and Drug Act of 1907; and (3) the remarkable achievement of providing safe water supplies for American cities by the end of the 1920s. The current expanding market for bottled water is based in part on bottled water being an alternative beverage Ito alcohol and sweetened drinks and the inconsistent palatability and perceived health hazards of some tap waters.

Water Chemistry and Chemistry Monitoring at Thermal and Nuclear Power Plants: Problems and Tasks (Based on Proceedings of Conferences)

Science.gov (United States)

Larin, B. M.

2018-02-01

In late May-early June 2017, two international science and technology conferences on problems of water chemistry and chemistry monitoring at thermal and nuclear power plants were held. The participants of both the first conference held at OAO VTI and the second conference that took place at NITI formulated the problems of the development of the regulatory base and implementation of promising water treatment technologies and outlined the ways of improving the water chemistry and chemistry monitoring at TPPs and NPPs for the near future. It was pointed out that the new amine-containing VTIAMIN agent developed by OAO VTI had been successfully tested on the power-generating units equipped with steam-gas plants to establish the minimum excess of the film-forming amine in the power-generating unit circuit that ensures the protection of the metal as 5-10 μg/dm3. A flow-injection technique for the analysis of trace concentrations of chlorides was proposed; the technique applied to the condensate of the 1000-MW steam turbine of the NPP power-generating unit yields the results comparable with the results obtained by the ion chromatography and the potentiometric method using the solver electrode. The participants of the conferences were demonstrated new Russian instruments to analyze the water media at the TPPs and NPPs, including the total organic carbon analyzer and the analyzer of mineral impurities in the condensate and feed water, that won a gold medal at the 45th International Exhibition of Inventions held in Geneva this April.

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.

Do airborne microbes matter for atmospheric chemistry and cloud formation?

Science.gov (United States)

Konstantinidis, Konstantinos T

2014-06-01

The role of airborne microbial cells in the chemistry of the atmosphere and cloud formation remains essentially speculative. Recent studies have indicated that microbes might be more important than previously anticipated for atmospheric processes. However, more work and direct communication between microbiologists and atmospheric scientists and modellers are necessary to better understand and model bioaerosol-cloud-precipitation-climate interactions. © 2014 Society for Applied Microbiology and John Wiley & Sons Ltd.

Secondary water chemistry control practices and results of the Japanese PWR plants

International Nuclear Information System (INIS)

Maeda, Akihiro; Shoda, Yasuhiko; Ishihara, Nobuo; Murata, Kazutoyo; Fujiwara, Hiroyuki; Hayakawa, Hitoshi; Matsuda, Tadashi

2012-09-01

In Japan, since the start of the operation of the first PWR plant, Mihama Unit-1 in 1970, 24 PWR plants have been built by 2010, and all of them are in operation. Due to the plant-specific needs of management, and by flexibly incorporating the state-of-the-art insights into the design, the system configurations of the plants vary so many as 15 types. Meanwhile, the geographical feature of Japan makes all the Japanese PWR plants to have condensers cooled by sea water, and all the plants have a common system with a full-flow Condensate Polisher System (CPS). To prevent corrosion, continued improvements of the secondary water chemistry management has been performed like other countries, and one of the major features of the Japanese PWR plants is an enhanced provision for the condenser leakage. The water quality of SG (Steam Generator) has been significantly improved by the provision for the sea water leakage, in combination with other improvements in water chemistry management. Also in Japan, almost all of the treatments of the spent polisher resin and the wastewater are performed within the power plant sites. To facilitate the treatment of the waste water and the regeneration of the spent resins, either ammonia or ETA (Ethanol Amine) is selected as the pH adjustment agent for the secondary system water. Also at the ammonia treatment, high pH accomplishes the inhibition of the piping wall thinning and the lower iron transportation into SGs. In addition, the iron transported into the SG is removed by the chemical conditioning treatment called ASCA (Advanced Scale Conditioning Agent). This provides the effective recovery of the SG heat-transfer performance, and the improved SG support plate BEC (Broached Egg Crate) hole blockage rates. Basically in Japan, the secondary water chemistry management has been improved based on a single basic specification, for the variety of the plant configurations, with the plant-specific investigations and analyses. This paper summarizes

Rock-Bound Arsenic Influences Ground Water and Sediment Chemistry Throughout New England

Science.gov (United States)

Robinson, Gilpin R.; Ayotte, Joseph D.

2007-01-01

The information in this report was presented at the Northeastern Region Geological Society of America meeting held March 11-14, 2007, in Durham, New Hampshire. In the New England crystalline bedrock aquifer, concentrations of arsenic that exceed the drinking water standard of 10 ?g/L occur most frequently in ground water from wells sited in specific metamorphic and igneous rock units. Geochemical investigations indicate that these geologic units typically have moderately elevated whole-rock concentrations of arsenic compared to other rocks in the region. The distribution of ground water wells with As > 5 ?g/L has a strong spatial correlation with specific bedrock units where average whole-rock concentrations of arsenic exceed 1.1 mg/kg and where geologic and geochemical factors produce high pH ground water. Arsenic concentrations in stream sediments collected from small drainages reflect the regional distribution of this natural arsenic source and have a strong correlation with both rock chemistry and the distribution of bedrock units with elevated arsenic chemistry. The distribution of ground water wells with As > 5 ?g/L has a strong spatial correlation with the distribution of stream sediments where concentrations of arsenic exceed 6 mg/kg. Stream sediment chemistry also has a weak correlation with the distribution of agricultural lands where arsenical pesticides were used on apple, blueberry, and potato crops. Elevated arsenic concentrations in bedrock wells, however, do not correlate with agricultural areas where arsenical pesticides were used. These results indicate that both stream sediment chemistry and the solubility and mobility of arsenic in ground water in bedrock are influenced by host-rock arsenic concentrations. Stream sediment chemistry and the distribution of geologic units have been found to be useful parameters to predict the areas of greatest concern for elevated arsenic in ground water and to estimate the likely levels of human exposure to

The Effect of Water Chemistry on the Removal of Arsenic from Drinking Water During Iron Removal Treatment

Science.gov (United States)

This research investigates the effects of water chemistry, oxidant type and concentration on the removal of iron and arsenic from drinking water. The research will be conducted using one of the National Risk Management Research Laboratory’s Water Supply and Water Resources Divisi...

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)

Effect of condenser water in-leakage on steam generator water chemistry

International Nuclear Information System (INIS)

Balakrishnan, P.V.

1978-01-01

Corrosive environments may be generated within steam genrators from condenser cooling water in-leakage. Theoretical as well as experimental evaluation of the aggressiveness of such environments is being carried out for the condenser-cooling waters used at CANDU-PHW nuclear power stations. Calculations have shown that highly concentrated chloride solutions - acidic in the case of sea-water in-leakage, and alkaline in the rest of the cases considered - would be produced within the steam generator. Experiments in a model boiler showed that sea-water in-leakage caused rapid corrosion of carbon steel components when only AVT (all volatile treatment) was used for water chemistry control. Use of a non-volatile reagent, as in the congruent phosphate treatment, avoided the rapid corrosion of carbon steel. On the basis of our studies, congruent phosphate treatment during sea water in-leakage appears desirable. (author)

Size distribution dynamics reveal particle-phase chemistry in organic aerosol formation

Science.gov (United States)

Shiraiwa, Manabu; Yee, Lindsay D.; Schilling, Katherine A.; Loza, Christine L.; Craven, Jill S.; Zuend, Andreas; Ziemann, Paul J.; Seinfeld, John H.

2013-01-01

Organic aerosols are ubiquitous in the atmosphere and play a central role in climate, air quality, and public health. The aerosol size distribution is key in determining its optical properties and cloud condensation nucleus activity. The dominant portion of organic aerosol is formed through gas-phase oxidation of volatile organic compounds, so-called secondary organic aerosols (SOAs). Typical experimental measurements of SOA formation include total SOA mass and atomic oxygen-to-carbon ratio. These measurements, alone, are generally insufficient to reveal the extent to which condensed-phase reactions occur in conjunction with the multigeneration gas-phase photooxidation. Combining laboratory chamber experiments and kinetic gas-particle modeling for the dodecane SOA system, here we show that the presence of particle-phase chemistry is reflected in the evolution of the SOA size distribution as well as its mass concentration. Particle-phase reactions are predicted to occur mainly at the particle surface, and the reaction products contribute more than half of the SOA mass. Chamber photooxidation with a midexperiment aldehyde injection confirms that heterogeneous reaction of aldehydes with organic hydroperoxides forming peroxyhemiacetals can lead to a large increase in SOA mass. Although experiments need to be conducted with other SOA precursor hydrocarbons, current results demonstrate coupling between particle-phase chemistry and size distribution dynamics in the formation of SOAs, thereby opening up an avenue for analysis of the SOA formation process. PMID:23818634

Size distribution dynamics reveal particle-phase chemistry in organic aerosol formation.

Science.gov (United States)

Shiraiwa, Manabu; Yee, Lindsay D; Schilling, Katherine A; Loza, Christine L; Craven, Jill S; Zuend, Andreas; Ziemann, Paul J; Seinfeld, John H

2013-07-16

Organic aerosols are ubiquitous in the atmosphere and play a central role in climate, air quality, and public health. The aerosol size distribution is key in determining its optical properties and cloud condensation nucleus activity. The dominant portion of organic aerosol is formed through gas-phase oxidation of volatile organic compounds, so-called secondary organic aerosols (SOAs). Typical experimental measurements of SOA formation include total SOA mass and atomic oxygen-to-carbon ratio. These measurements, alone, are generally insufficient to reveal the extent to which condensed-phase reactions occur in conjunction with the multigeneration gas-phase photooxidation. Combining laboratory chamber experiments and kinetic gas-particle modeling for the dodecane SOA system, here we show that the presence of particle-phase chemistry is reflected in the evolution of the SOA size distribution as well as its mass concentration. Particle-phase reactions are predicted to occur mainly at the particle surface, and the reaction products contribute more than half of the SOA mass. Chamber photooxidation with a midexperiment aldehyde injection confirms that heterogeneous reaction of aldehydes with organic hydroperoxides forming peroxyhemiacetals can lead to a large increase in SOA mass. Although experiments need to be conducted with other SOA precursor hydrocarbons, current results demonstrate coupling between particle-phase chemistry and size distribution dynamics in the formation of SOAs, thereby opening up an avenue for analysis of the SOA formation process.

Water chemistry data acquisition, processing, evaluation and diagnostic systems in Light Water Reactors: Future improvement of plant reliability and safety

International Nuclear Information System (INIS)

Uchida, S.; Takiguchi, H.; Ishigure, K.

2006-01-01

Data acquisition, processing and evaluation systems have been applied in major Japanese PWRs and BWRs to provide (1) reliable and quick data acquisition with manpower savings in plant chemical laboratories and (2) smooth and reliable information transfer among chemists, plant operators, and supervisors. Data acquisition systems in plants consist of automatic and semi-automatic instruments for chemical analyses, e. g., X-ray fluorescence analysis and ion chromatography, while data processing systems consist of PC base-sub-systems, e.g., data storage, reliability evaluation, clear display, and document preparation for understanding the plant own water chemistry trends. Precise and reliable evaluations of water chemistry data are required in order to improve plant reliability and safety. For this, quality assurance of the water chemistry data acquisition system is needed. At the same time, theoretical models are being applied to bridge the gaps between measured water chemistry data and the information desired to understand the interaction of materials and cooling water in plants. Major models which have already been applied for plant evaluation are: (1) water radiolysis models for BWRs and PWRs; (2) crevice radiolysis model for SCC in BWRs; and (3) crevice pH model for SG tubing in PWRs. High temperature water chemistry sensors and automatic plant diagnostic systems have been applied in only restricted areas. ECP sensors are gaining popularity as tools to determine the effects of hydrogen injection in BWR systems. Automatic plant diagnostic systems based on artificial intelligence will be more popular after having sufficient experience with off line diagnostic systems. (author)

Chemistry of reference waters of the crystalline basement of Northern Switzerland for safety assessment studies

International Nuclear Information System (INIS)

Pearson, F.J. Jr.; Scholtis, A.

1993-08-01

The chemistry of groundwater in formations being considered as host rocks for nuclear waste repositories must be known to assess the performance of those repositories, and as media for laboratory experiments. Two potential repository siting areas in the crystalline basement of northern Switzerland are being assessed. This report gives the chemistry of water in both areas for reference use in this assessment. The western area is in the region defined by the Kaisten, Leuggern, Boettstein, and Zurzach boreholes. The western reference water is based on samples from the Leuggern, Boettstein, and Zurzach boreholes. Kaisten water is of higher salinity (1.3 g/l). The concentration ranges of the reference water include Kaisten values, however. High quality samples and analyses, particularly from long term sampling at Zurzach and Leuggern, define the concentration ranges of many trace elements. The definition of this water assumes saturation with respect to calcite, baryte, fluorites, chalcedony, and kaolinite. The reference pe is based on the assumption that dissolved iron concentrations are controlled by the solubility of the mineral goethite, and is consistent with other redox indicators such as the measured Pt-electrode potential and the ratio of dissolved As(V) to As(III). The eastern area is characterized by the Siblingen boreholes. The eastern reference water is a Na-HCO 3 -SO 4 -(Cl) type with a total dissolved solids content of about 0.5 g/l. Only three samples taken during borehole drilling are available to define this water, so it can be specified in less detail and with less precision than the western water. Its definition assumes saturation with respect to calcite, baryte, and fluorites. The samples permit only a broad definition of its oxidation potential and content of redox-sensitive metals such as Fe, As, Mn, and U. Trace element data for the most part are lacking. (author) figs., tabs., 28 refs

Steam turbine chemistry in light water reactor plants

International Nuclear Information System (INIS)

Svoboda, Robert; Haertel, Klaus

2008-01-01

Steam turbines in boiling water reactor (BWR) and pressurized water reactor (PWR) power plants of various manufacturers have been affected by corrosion fatigue and stress corrosion cracking. Steam chemistry has not been a prime focus for related research because the water in nuclear steam generating systems is considered to be of high purity. Steam turbine chemistry however addresses more the problems encountered in fossil fired power plants on all volatile treatment, where corrosive environments can be formed in zones where wet steam is re-evaporated and dries out, or in the phase transition zone, where superheated steam starts to condense in the low-pressure (LP) turbine. In BWR plants the situation is aggravated by the fact that no alkalizing agents are used in the cycle, thus making any anionic impurity immediately acidic. This is illustrated by case studies of pitting corrosion of a 12 % Cr steel gland seal and of flow-oriented corrosion attack on LP turbine blades in the phase transition zone. In PWR plants, volatile alkalizing agents are used that provide some buffering of acidic impurities, but they also produce anionic decomposition products. (orig.)

Optimum Water Chemistry in radiation field buildup control

Energy Technology Data Exchange (ETDEWEB)

Lin, Chien, C. [Vallecitos Nuclear Center, Pleasanton, CA (United States)

1995-03-01

Nuclear utilities continue to face the challenGE of reducing exposure of plant maintenance personnel. GE Nuclear Energy has developed the concept of Optimum Water Chemistry (OWC) to reduce the radiation field buildup and minimize the radioactive waste production. It is believed that reduction of radioactive sources and improvement of the water chemistry quality should significantly reduce both the radiation exposure and radwaste production. The most important source of radioactivity is cobalt and replacement of cobalt containing alloy in the core region as well as in the entire primary system is considered the first priority to achieve the goal of low exposure and minimized waste production. A plant specific computerized cobalt transport model has been developed to evaluate various options in a BWR system under specific conditions. Reduction of iron input and maintaining low ionic impurities in the coolant have been identified as two major tasks for operators. Addition of depleted zinc is a proven technique to reduce Co-60 in reactor water and on out-of-core piping surfaces. The effect of HWC on Co-60 transport in the primary system will also be discussed.

The influence of water chemistry and biocide additions on the response of an on-line biofilm monitor

International Nuclear Information System (INIS)

Licina, G.J.; Nekoksa, G.

1995-01-01

Microbiologically influenced corrosion (MIC) is a significant cause of degradation of piping and heat transfer surfaces in cooling water systems. The interaction between the metabolic processes of microorganisms attached to metallic surfaces and corrosion processes can lead to localized corrosion and rapid penetration of piping and heat exchanger tubes. On-line Monitoring of biofilm formation on Metallic Surfaces is a key both for automatic control equipment and for system operators so that mitigation activities can be initiated well before the structural integrity of piping or components is jeopardized. In addition, tracking of biofilm activity on line provides feedback useful for evaluating the effectiveness of biocide additions and optimizing the concentrations and addition schedules of biocides and other control chemicals. A probe has been developed to provide a method for determining the onset of biofilm formation on metal surfaces and tracking biofilm activity on line in a power plant or industrial environment; in fresh water and seawater environments. Experience with the system in a variety of water chemistries, and system responses to biofilm growth and subsequent destruction by biocide additions are described

Water chemistry in WWER reactors

International Nuclear Information System (INIS)

Yurmanov, V.A.; Mamet, V.A.; Shestakov, Yu.M.; Amosov, M.M.

1997-01-01

In this paper ''Water Chemistry in WWER Reactors'', are briefly described the 30 WWERs in Russian and the Ukraine, and are pointed out the essential differences between the 440s and 1000s. The primary coolant in the six loops of the former type operates at 270-290 deg. C, while the four loops of the latter type are at 290-320 deg. C. Performance of the fuel has been generally good with some fission product activities emanating from tramp uranium. Incidents causing unusually high fission product levels were overheating of the 16th fuel load at Kola NPP in 1990 by a reduced coolant flow, and fuel defects at Novovoronezh NPP resulting from deposits of carbon and corrosion products. Organic carbon, depositing from the coolant in regions of high turbulence (i.e. at the spacer grids), provokes corrosion product deposition. The source of the organic is not known. New chemistry guidelines have been implemented since 1992-93 for Russian and Ukrainian WWERs. These include higher pH T values (7.0-7.1 as opposed to 6.6-6.9) and tighter controls on oxygen and impurities. Lower dose rates in steam generator channels are reported. Significant reduction in operator doses are achieved by these methods coupled with a ''soft decontamination'' involving changing the KOH concentration and, hence, the pH T before shutdown. The benefits of hydrazine treatment for deoxygenating feedwater and coolant prior to start up, for injecting before shutdown and for general chemistry control on radiation fields are described. (author). 7 refs, 9 figs, 8 tabs

Water chemistry in WWER reactors

Energy Technology Data Exchange (ETDEWEB)

Yurmanov, V A; Mamet, V A; Shestakov, Yu M; Amosov, M M [All-Russian Scientific Research Inst. for Nuclear Power Plants Operation, Moscow (Russian Federation)

1997-02-01

In this paper ``Water Chemistry in WWER Reactors``, are briefly described the 30 WWERs in Russian and the Ukraine, and are pointed out the essential differences between the 440s and 1000s. The primary coolant in the six loops of the former type operates at 270-290 deg. C, while the four loops of the latter type are at 290-320 deg. C. Performance of the fuel has been generally good with some fission product activities emanating from tramp uranium. Incidents causing unusually high fission product levels were overheating of the 16th fuel load at Kola NPP in 1990 by a reduced coolant flow, and fuel defects at Novovoronezh NPP resulting from deposits of carbon and corrosion products. Organic carbon, depositing from the coolant in regions of high turbulence (i.e. at the spacer grids), provokes corrosion product deposition. The source of the organic is not known. New chemistry guidelines have been implemented since 1992-93 for Russian and Ukrainian WWERs. These include higher pH{sub T} values (7.0-7.1 as opposed to 6.6-6.9) and tighter controls on oxygen and impurities. Lower dose rates in steam generator channels are reported. Significant reduction in operator doses are achieved by these methods coupled with a ``soft decontamination`` involving changing the KOH concentration and, hence, the pH{sub T} before shutdown. The benefits of hydrazine treatment for deoxygenating feedwater and coolant prior to start up, for injecting before shutdown and for general chemistry control on radiation fields are described. (author). 7 refs, 9 figs, 8 tabs.

Technical specifications for PWR secondary water chemistry

International Nuclear Information System (INIS)

Weeks, J.R.; van Rooyen, D.

1977-08-01

The bases for establishing Technical Specifications for PWR secondary water chemistry are reviewed. Whereas extremely stringent control of secondary water needs to be maintained to prevent denting in some units, sound bases for establishing limits that will prevent stress corrosion, wastage, and denting do not exist at the present time. This area is being examined very thoroughly by industry-sponsored research programs. Based on the evidence available to date, short term control limits are suggested; establishment of these or other limits as Technical Specifications is not recommended until the results of the research programs have been obtained and evaluated

Variation of the Effectiveness of Hydrogen Water Chemistry in a Boiling Water Reactor during Startup Operations

International Nuclear Information System (INIS)

Yeh, Tsung-Kuang; Wang, Mei-Ya

2012-09-01

For mitigating intergranular stress corrosion cracking (IGSCC) in an operating boiling water reactor (BWR), the technology of hydrogen water chemistry (HWC) aiming at coolant chemistry improvement has been adopted worldwide. However, the hydrogen injection system employed in this technology was designed to operate only at power levels greater than 30% of the rated power or at coolant temperatures of greater than 450 deg. F. This system is usually in an idle and standby mode during a startup operation. The coolant in a BWR during a cold shutdown normally contains a relatively high level of dissolved oxygen from intrusion of atmospheric air. Accordingly, the structural materials in the primary coolant circuit (PCC) of a BWR could be exposed to a strongly oxidizing environment for a short period of time during a subsequent startup operation. At some plants, the feasibility of hydrogen water chemistry during startup operations has been studied, and its effectiveness on suppressing SCC initiation was evaluated. It is technically difficult to directly procure water chemistry data at various locations of an operating reactor. Accordingly, the impact of startup operation on water chemistry in the PCC of a BWR operating under normal water chemistry (NWC) or HWC can only be theoretically evaluated through computer modelling. In this study, a well-developed computer code DEMACE was used to investigate the variations in redox species concentration and in electrochemical corrosion potential (ECP) of components in the PCC of a domestic BWR during startup operations in the presence of HWC. Simulations were carried out for [H2] FW s ranging from 0.0 to 2.0 parts per million (ppm) and for power levels ranging from 2.5% to 11.3% during startup operations. Our analyses indicated that for power levels with steam generation in the core, a higher power level would tend to promote a more oxidizing coolant environment for the structural components and therefore lead to less HWC

Collaborative routes to clarifying the murky waters of aqueous supramolecular chemistry.

Science.gov (United States)

Cremer, Paul S; Flood, Amar H; Gibb, Bruce C; Mobley, David L

2017-12-19

On planet Earth, water is everywhere: the majority of the surface is covered with it; it is a key component of all life; its vapour and droplets fill the lower atmosphere; and even rocks contain it and undergo geomorphological changes because of it. A community of physical scientists largely drives studies of the chemistry of water and aqueous solutions, with expertise in biochemistry, spectroscopy and computer modelling. More recently, however, supramolecular chemists - with their expertise in macrocyclic synthesis and measuring supramolecular interactions - have renewed their interest in water-mediated non-covalent interactions. These two groups offer complementary expertise that, if harnessed, offer to accelerate our understanding of aqueous supramolecular chemistry and water writ large. This Review summarizes the state-of-the-art of the two fields, and highlights where there is latent chemical space for collaborative exploration by the two groups.

Collaborative routes to clarifying the murky waters of aqueous supramolecular chemistry

Science.gov (United States)

Cremer, Paul S.; Flood, Amar H.; Gibb, Bruce C.; Mobley, David L.

2018-01-01

On planet Earth, water is everywhere: the majority of the surface is covered with it; it is a key component of all life; its vapour and droplets fill the lower atmosphere; and even rocks contain it and undergo geomorphological changes because of it. A community of physical scientists largely drives studies of the chemistry of water and aqueous solutions, with expertise in biochemistry, spectroscopy and computer modelling. More recently, however, supramolecular chemists -- with their expertise in macrocyclic synthesis and measuring supramolecular interactions -- have renewed their interest in water-mediated non-covalent interactions. These two groups offer complementary expertise that, if harnessed, offer to accelerate our understanding of aqueous supramolecular chemistry and water writ large. This Review summarizes the state-of-the-art of the two fields, and highlights where there is latent chemical space for collaborative exploration by the two groups.

IAEA interlaboratory exercise for water chemistry

International Nuclear Information System (INIS)

Joe, Kih Soo; Choi, Kwang Soon; Han, Sun Ho; Suh, Moo Yul; Jeon, Young Shin; Choi, Ke Chun; Kim, Yong Bok; Kim, Jong Gu; Kim, Won Ho

2003-09-01

KAERI Analytical laboratory participated in the IAEA Interlaboratory exercise for water chemistry of groundwater(RAS/8/084). 13 items such as pH, electroconductivity, HCO 3 , Cl, SO 4 , SiO 2 , B, Li, Na, K, Ca, Mg and NH 3 were analyzed. The result of this exercise showed that KAERI laboratory was ranked on the top level of the participants. Major analytical methods applied for this activity were ICP-AES, AAS, IC, pH meter, conductometer and acid titration

Relationships between water and gas chemistry in mature coalbed methane reservoirs of the Black Warrior Basin

Science.gov (United States)

Pashin, Jack C.; McIntyre-Redden, Marcella R.; Mann, Steven D.; Kopaska-Merkel, David C.; Varonka, Matthew S.; Orem, William H.

2014-01-01

Water and gas chemistry in coalbed methane reservoirs of the Black Warrior Basin reflects a complex interplay among burial processes, basin hydrodynamics, thermogenesis, and late-stage microbial methanogenesis. These factors are all important considerations for developing production and water management strategies. Produced water ranges from nearly potable sodium-bicarbonate water to hypersaline sodium-chloride brine. The hydrodynamic framework of the basin is dominated by structurally controlled fresh-water plumes that formed by meteoric recharge along the southeastern margin of the basin. The produced water contains significant quantities of hydrocarbons and nitrogen compounds, and the produced gas appears to be of mixed thermogenic-biogenic origin.Late-stage microbial methanogenesis began following unroofing of the basin, and stable isotopes in the produced gas and in mineral cements indicate that late-stage methanogenesis occurred along a CO2-reduction metabolic pathway. Hydrocarbons, as well as small amounts of nitrate in the formation water, probably helped nourish the microbial consortia, which were apparently active in fresh to hypersaline water. The produced water contains NH4+ and NH3, which correlate strongly with brine concentration and are interpreted to be derived from silicate minerals. Denitrification reactions may have generated some N2, which is the only major impurity in the coalbed gas. Carbon dioxide is a minor component of the produced gas, but significant quantities are dissolved in the formation water. Degradation of organic compounds, augmented by deionization of NH4+, may have been the principal sources of hydrogen facilitating late-stage CO2 reduction.

The chemistry of salt-affected soils and waters

Science.gov (United States)

Knowledge of the chemistry of salt affected soils and waters is necessary for management of irrigation in arid and semi-arid regions. In this chapter we review the origin of salts in the landscape, the major chemical reactions necessary for prediction of the soil solution composition, and the use of...

Expert System for Diagnostics and Status Monitoring of NPP Water Chemistry Condition

International Nuclear Information System (INIS)

Shvedova, M.N.; Kritski, V.G.; Zakharova, S.V.; Nikolaev, F.V.; Benediktov, V.B.

2002-01-01

Water chemistry condition (WCC) has been the subject of constant study and improvement up to the present day. It is connected with the presence of a direct relationship between the violation of water chemistry regulation on the one hand and components reliability of the circuit's equipment and cost-effectiveness of their operation on the other. It dictates the necessity to apply different optimization methods in the field of monitoring and use of information - analytical and diagnostic systems to assess WCC quality, control and support. By now NPP experts have broad experience in revealing and removing the causes of WCC disturbances. However this knowledge is often of an intuitive, non-classified nature, scattered among various working documents, which makes their transfer difficult. Based on what has been mentioned above, special attention is currently being paid to the problem of creating expert diagnostic systems for supporting the optimum WCC. The existing developments in this field (DIWA, Smart chem Works, the water quality control system at the Onagava NPP etc. [1,3,4,5] are based on wide use of experts' knowledge. Such expert diagnostic systems for supporting WCC refer to the new generation of intellectual control methods, which allow the incorporation of the latest achievements both in the field of water chemistry simulation and in the field of artificial intelligence and computer technologies. LI 'VNIPIET' employees have, for several years, been developing an expert diagnostic system for supporting WCC and status monitoring of RBMK - reactor NPPs [2]. This system has not only conveniently organized the traditional functions of information acquisition and storage, a complete presentation of information in the form of tables, graphs of a dynamical changes of parameters and formation regular reports, diagnostic functions and issuing recommendations on WCC correction, but it also allows the assessment of confidence in the diagnosis made, relying on a wide

Water Chemistry Control Technology to Improve the Performance of Nuclear Power Plants for Extended Fuel Cycles

International Nuclear Information System (INIS)

Maeng, W. Y.; Na, J. W.; Lee, E. H.

2010-07-01

Ο To Develop the technology to manage the problems of AOA and radiation, corrosion as long term PWR operation. Ο To Establish the advanced water chemical operating systems. - Development of the proper water chemistry guidelines for long term PWR operation. AOA(Axial Offest Anomaly) has been reported in many PWR plants in the world, including Korea, especially in the plants of higher burn-up and longer cycle operation or power up-rate. A test loop has been designed and made by KAERI, in order to investigate and mitigate AOA problems in Korea. This project included the study of hydrodynamic simulation and the modeling about AOA. The analysis of radioactive crud was performed to investigate of NPPs primary water chemical effect on AOA and to reduce the radioactive dose rate. The high temperature measurement system was developed to on-line monitor of water chemistry in nuclear power plants. The effects of various environmental factors such as temperature, pressure, and flow rate on YSZ-based pH electrode were evaluated for ensuring the accuracy of high-temperature pH measurement. The inhibition technology for fouling and SCC of SG tube was evaluated to establish the water chemistry technology of corrosion control of nuclear system. The high temperature and high pressure crevice chemistry analysis test loop was manufactured to develop the water chemistry technology of crevice chemistry control

Water analysis

International Nuclear Information System (INIS)

Garbarino, J.R.; Steinheimer, T.R.; Taylor, H.E.

1985-01-01

This is the twenty-first biennial review of the inorganic and organic analytical chemistry of water. The format of this review differs somewhat from previous reviews in this series - the most recent of which appeared in Analytical Chemistry in April 1983. Changes in format have occurred in the presentation of material concerning review articles and the inorganic analysis of water sections. Organic analysis of water sections are organized as in previous reviews. Review articles have been compiled and tabulated in an Appendix with respect to subject, title, author(s), citation, and number of references cited. The inorganic water analysis sections are now grouped by constituent using the periodic chart; for example, alkali, alkaline earth, 1st series transition metals, etc. Within these groupings the references are roughly grouped by instrumental technique; for example, spectrophotometry, atomic absorption spectrometry, etc. Multiconstituent methods for determining analytes that cannot be grouped in this manner are compiled into a separate section sorted by instrumental technique. References used in preparing this review were compiled from nearly 60 major journals published during the period from October 1982 through September 1984. Conference proceedings, most foreign journals, most trade journals, and most government publications are excluded. References cited were obtained using the American Chemical Society's Chemical Abstracts for sections on inorganic analytical chemistry, organic analytical chemistry, water, and sewage waste. Cross-references of these sections were also included. 860 references

Technical basis for hydrogen-water chemistry: Laboratory studies of water chemistry effects on SCC [stress-corrosion-cracking

International Nuclear Information System (INIS)

Kassner, T.F.; Ruther, W.E.; Soppet, W.K.

1986-10-01

The influence of different impurities, viz., oxyacids and several chloride salts, on the stress-corrosion-cracking (SCC) of sensitized Type 304 stainless steel (SS) was investigated in constant-extension-rate-tensile (CERT) tests in 289 0 C water at a low dissolved-oxygen concentration ( 0 C in low-oxygen environments with and without sulfate at low concentrations. In these experiments, the crack growth behavior of the materials was correlated with the type and concentration of the impurities and the electrochemical potentials of Type 304 SS and platinum electrodes in the simulated hydrogen-water chemistry environments. The information suggests that better characterization of water quality, through measurement of the concentrations of individual species (SO 4 2- , NO 3 - , Cu 2+ , etc.) coupled with measurements of the corrosion and redox potentials at high temperatures will provide a viable means to monitor and ultimately improve the performance of BWR system materials

Scientific basis for the choice of primary/secondary water chemistry

International Nuclear Information System (INIS)

Garnsey, R.

1988-01-01

The purpose of this paper is to illustrate the common scientific basis for the chemistry control strategies which have been developed. The evolution of chemistry control philosophies in some plant designs are outlined as examples. The essential requirement of water chemistry control is to preserve integrity of the circuit under all the environmental conditions experienced within that circuit. There may be specific additional requirements, as in the case of a PWR primary circuit, where boron concentration is used to control reactivity. The crucial requirement or concern can vary. In the primary circuit of a light water reactor the crucial requirement is to supress the activation and transportation of corrosion products and so minimize radiation fields around the circuit. On the secondary side of recirculating steam generators the critical requirement has been to preserve the integrity of generator tubing. In once-through steam generators the critical requirement may be the control of pressure losses associated with corrosion product deposits in the steam generator and the integrity of the turbine in addition to boiler integrity. (Nogami, K.)

Investigating the pore-water chemistry effects on the volume change behaviour of Boom clay

Science.gov (United States)

Deng, Y. F.; Cui, Y. J.; Tang, A. M.; Nguyen, X. P.; Li, X. L.; Van Geet, M.

The Essen site has been chosen as an alternative site for nuclear waste disposal in Belgium. The soil formation involved at this site is the same as at Mol site: Boom clay. However, owing to its geographical situation closer to the sea, Boom clay at Essen presents a pore water salinity 4-5 times higher than Boom clay at Mol. This study aims at studying the effects of pore water salinity on the hydro-mechanical behaviour of Boom clay. Specific oedometer cells were used allowing “flushing” the pore water in soil specimen by synthetic pore water or distilled water. The synthetic pore water used was prepared with the chemistry as that for the site water: 5.037 g/L for core Ess83 and 5.578 g/L for core Ess96. Mechanical loading was then carried out on the soil specimen after flushing. The results show that water salinity effect on the liquid limit is negligible. The saturation or pore water replacement under the in situ effective stress of 2.4 MPa does not induce significant volume change. For Ess83, hydro-mechanical behaviour was found to be slightly influenced by the water salinity; on the contrary, no obvious effect was identified on the hydro-mechanical behaviour of Ess96. This can be attributed to the higher smectite content in Ess83 than in Ess96.

The research of materials and water chemistry for supercritical water-cooled reactors in Research Centre Rez

International Nuclear Information System (INIS)

Zychova, Marketa; Fukac, Rostislav; Vsolak, Rudolf; Vojacek, Ales; Ruzickova, Mariana; Vonkova, Katerina

2012-09-01

Research Centre Rez (CVR) is R and D company based in the Czech Republic. It was established as the subsidiary of the Nuclear Research Institute Rez plc. One of the main activities of CVR is the research of materials and chemistry for the generation IV reactor systems - especially the supercritical water-cooled one. For these experiments is CVR equipped by a supercritical water loop (SCWL) and a supercritical water autoclave (SCWA) serving for research of material and Supercritical Water-cooled Reactor (SCWR) environment compatibility experiments. SCWL is a research facility designed to material, water chemistry, radiolysis and other testing in SCWR environment, SCWA serves for complementary and supporting experiments. SCWL consists of auxiliary circuits (ensuring the required parameters as temperature, pressure and chemical conditions in the irradiation channel, purification and measurements) and irradiation channel (where specimens are exposed to the SCWR environment). The design of the loop is based on many years of experience with loop design for various types of corrosion/water chemistry experiments. Designed conditions in the test area of SCWL are 600 deg. C and 25 MPa. SCWL was designed in 2008 within the High Performance Light Water Reactor Phase 2 project and built during 2008 and 2009. The trial operations were performed in 2010 and 2011 and were divided into three phases - the first phase to verify the functionality of auxiliary circuits of the loop, the second phase to verify the complete facility (auxiliary circuits and functional irradiation channel internals) and the third phase to verify the feasibility of corrosion tests with the complete equipment and specimens. All three trial operations were very successful - designed conditions and parameters were reached. (authors)

Oxide/water interfaces: how the surface chemistry modifies interfacial water properties

International Nuclear Information System (INIS)

Gaigeot, Marie-Pierre; Sprik, Michiel; Sulpizi, Marialore

2012-01-01

The organization of water at the interface with silica and alumina oxides is analysed using density functional theory-based molecular dynamics simulation (DFT-MD). The interfacial hydrogen bonding is investigated in detail and related to the chemistry of the oxide surfaces by computing the surface charge density and acidity. We find that water molecules hydrogen-bonded to the surface have different orientations depending on the strength of the hydrogen bonds and use this observation to explain the features in the surface vibrational spectra measured by sum frequency generation spectroscopy. In particular, ‘ice-like’ and ‘liquid-like’ features in these spectra are interpreted as the result of hydrogen bonds of different strengths between surface silanols/aluminols and water. (paper)

Proceedings of the water chemistry and materials performance conference

International Nuclear Information System (INIS)

Barber, D.

1986-01-01

The proceedings contain 11 papers dealing with primary and secondary side water chemistry in CANDU reactors, with the associated problems of activity transport and steam generator corrosion, and also with the use of decontaminating solutions. The individual papers have been abstracted separately

Proceedings of the water chemistry and materials performance conference

Energy Technology Data Exchange (ETDEWEB)

Barber, D [ed.; Atomic Energy of Canada Ltd., Sheridan Park, ON (Canada). CANDU Operations

1987-12-31

The proceedings contain 11 papers dealing with primary and secondary side water chemistry in CANDU reactors, with the associated problems of activity transport and steam generator corrosion, and also with the use of decontaminating solutions. The individual papers have been abstracted separately.

Water chemistry related problems in captive power plant of Heavy Water Plant [Manuguru

International Nuclear Information System (INIS)

Prasada Rao, G.; Mohapatra, C.

2000-01-01

This study is intended to improve the power generating capacity of Turbo Generator-3 in CPP. It was observed that steam flow through TG-3 was not as per rated; however there were no abnormal vibrations. After stopping and opening the turbine, deposits were found on turbine blade. Turbine blade scales were analysed for all the stages, HP, middle, LP, casings. Boiler drum water, feed water, DM water, filter water chemistry were studied. LP blade scale mainly consists of silica, whereas HP blade scale consists of iron oxide, sodium phosphate, silica etc. It was concluded that less generating capacity of power was because of scaling on turbine blade. (author)

The hydrochemistry of glacial Ebba River (Petunia Bay, Central Spitsbergen): Groundwater influence on surface water chemistry

Science.gov (United States)

Dragon, Krzysztof; Marciniak, Marek; Szpikowski, Józef; Szpikowska, Grażyna; Wawrzyniak, Tomasz

2015-10-01

The article presents the investigation of surface water chemistry changes of the glacial Ebba River (Central Spitsbergen) during three melting seasons of 2008, 2009 and 2010. The twice daily water chemistry analyses allow recognition of the surface water chemistry differentiation. The surface water chemistry changes are related to the river discharge and changes in the influence of different water balance components during each melting season. One of the most important process that influence river water component concentration increase is groundwater inflow from active layer occurring on the valley area. The significance of this process is the most important at the end of the melting season when temperatures below 0 °C occur on glaciers (resulting in a slowdown of melting of ice and snow and a smaller recharge of the river by the water from the glaciers) while the flow of groundwater is still active, causing a relatively higher contribution of groundwater to the total river discharge. The findings presented in this paper show that groundwater contribution to the total polar river water balance is more important than previously thought and its recognition allow a better understanding of the hydrological processes occurring in a polar environment.

Apparatus for ground water chemistry investigations in field caissons

International Nuclear Information System (INIS)

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

Effect of water chemistry on deposition for PWR plant operation

International Nuclear Information System (INIS)

Le Calvar, Marc; Bretelle, J. L.; Cailleaux, J. P.; Lacroix, R.; Guivarch, M.; Gay, N.; Taunier, S.; Gressier, F.; Varry, P.; Corredera, G.; Alos-Ramos, O.; Dijoux, M.

2012-09-01

For Pressurized Water Reactor (PWR) operation, water chemistry guidelines, specifications and associated surveillance programs are key to avoid deposition of oxides. Deposition of oxides can be detrimental by disrupting results of flow measurements, decreasing the thermal exchange capacity, or even by impairing safety. This paper describes the most important cases of deposition, their consequences for operation, and the implemented improvements to avoid their reoccurrence. Deposition that led to a Crud Induced Power Shift (CIPS) is also described. In the primary and in the secondary sides, orifice plates are typically used for measuring feedwater flow rate in nuclear power plants. Feedwater flow rates are used for control purposes and are important safety parameters as they are used to determine the plant's operating power level. Fouling of orifice plates in the primary side has been found during surveillance testing. For reactor coolant pumps, the formation of deposits on the seal No.1 can cause abnormally high or low leak rates through the seal. The leak rate through this seal must be carefully maintained within a prescribed range during plant operation. In the secondary side, orifice plate fouling has been the cause of feedwater flow/reference thermal power drift. For the steam generators (SG), magnetite deposition has led to fouling of the tube bundle, clogging of the quadri-foiled support plate holes and hard sludge formation on the base plate. For the generators, copper hollow conductors are widely used. Buildup of copper oxides on the interior walls of copper conductors has caused insufficient heat transfer. All these deposition cases have received adequate attention, understanding and response via improvement of our surveillance programs. (authors)

Mutual complementation between water chemistry and isotope techniques

International Nuclear Information System (INIS)

Matthess, G.

1976-01-01

In the water chemistry and isotope methods which applied together enable more extensive statements to be made than each on its own, the following regions of cooperation are brought out: 1) Isotopes as conservative indicators a) microbial decomposition of organic substances in the anaerobic and aerobic region; b) precipitation and coprecipitation; c) mechanical filtration, adsorption and coprecipitation; d) gas exchange; e) dilution by infiltration; 2) geochemical observations as additional basis for isotope investigations; 3) the investigation of the water content substances as additional help to isotope hydrology. (HK/LH) [de

Materials behavior in alternate (hydrogen) water chemistry in the Ringhals-1 boiling water reactor

International Nuclear Information System (INIS)

Ljungberg, L.G.; Cubicciotti, D.; Trolle, M.

1986-01-01

In-plant studies on the intergranular stress corrosion cracking (IGSCC) of sensitized austenitic stainless steel (SS) have been performed at the Swedish Ringhals-1 boiling water reactor (BWR). The studies have covered the present [full-temperature (normal)] water chemistry (PWC) and the alternate (primary) water chemistry (AWC) with hydrogen addition. The test techniques applied were constant extension rate testing (CERT) and electrochemical potential (ECP) measurements. The program was covered by extensive environment monitoring. The results verify earlier laboratory studies which show that sensitized austenitic SS is susceptible to IGSCC in PWC, but not in AWC. Other pressure-bearing BWR construction materials are not adversely affected by AWC. The boundary conditions in Ringhals-1 have been established for an AWC, which is defined as an environment that does not produce IGSCC in sensitized SS. The results are compared with a similar program at Dresden-2, and the points of agreement and discordance in the results are discussed. The relevance of ECP measurements for the control of AWC is discussed

Aqueous chemistry of chlorine: chemistry, analysis, and environmental fate of reactive oxidant species

Energy Technology Data Exchange (ETDEWEB)

Jolley, R.L.; Carpenter, J.H.

1982-01-01

This report reviews (1) the chemistry of chlorine relative to its reactions in fresh, estuarine, and marine waters and the formation of reactive oxidant species; (2) the current status of chemical analysis of reactive chlorine species and chlorine-produced oxidant species relative to analysis of low concentrations (microgram-per-liter range) and determination of accuracy and precision of methods; and (3) the environmental fate of chlorine and chlorine-produced oxidant species.

An evaluation of selection criteria on primary water chemistry parameters for SMART

International Nuclear Information System (INIS)

Choi, B. S.; Kim, S. H.; Yun, J. H.; Bae, Y. Y.; Gee, S. G.

2003-01-01

The selection criteria on the primary water chemistry of SMART by comparing the chemical design features with those of the current operating PWRs is analyzed. The most essential differences in water chemistry between the PWRs and SMART reactor is characterized by the presence of boron in water. SMART is boron free reactor, and the ammonia is used as a pH reagent. In SMART reactor hydrogen gas is not added to the primary coolant, but is normally generated from the radiolysis of ammonia of the coolant passes through the core. Ammonia is added once per shift because SMART reactor has no letdown and charging system during power operation. Because of these competing processes, the concentrations of hydrogen, nitrogen and ammonia in the primary coolant are steady state concentrations, which depend on the decomposition/combination rate of ammonia. Ammonia chemistry in SMART reactor has many advantages in that no hydrogen gas injection is needed to control the dissolved oxygen in primary coolant because of spontaneous generation of hydrogen and nitrogen produced by the reaction of ammonia decomposition

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, Robert 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

Decontamination flange film characterization for a boiling water reactor under hydrogen water chemistry

International Nuclear Information System (INIS)

Baston, V.F.; Garbauskas, M.F.; Bozeman, J.

1996-01-01

Stainless steel artifacts removed from a boiling water reactor class 4 plant that operated under hydrogen water chemistry and experienced a difficult decontamination were submitted for oxide film characterization. The results reported for the corrosion film composition and structure are consistent with existing theoretical concepts for stainless steel corrosion, spinel structure site preferences (octahedral or tetrahedral) for transition metal ions, and potential-pH diagrams. The observed zinc effects on film stability and lower cobalt incorporation are also consistent with these theoretical concepts

Biofilm formation in a hot water system

DEFF Research Database (Denmark)

Bagh, L.K.; Albrechtsen, Hans-Jørgen; Arvin, Erik

2002-01-01

The biofilm formation rate was measured in situ in a hot water system in an apartment building by specially designed sampling equipment, and the net growth of the suspended bacteria was measured by incubation of water samples with the indigeneous bacteria. The biofilm formation rate reached......, in the sludge, or in the water from the distribution system was negligible. This indicated that bacterial growth took place on the inner surfaces in the hot water system and biofilm formation and detachment of bacteria could account for most of the suspended bacteria actually measured in hot water. Therefore...

Fundamental R and D program on water chemistry of supercritical pressure water under radiation field

International Nuclear Information System (INIS)

Katsumura, Yosuke; Kiuchi, Kiyoshi; Wada, Yoichi; Yotsuyanagi, Tadasu

2003-01-01

In a supercritical water-cooled reactor, property of water changes significantly around the critical point. It is expected that irradiation and change of water property will affect the chemistry and material corrosion. Deep understanding of interactions between supercritical water and materials under irradiation is important. However, comprehensive data on radiolysis, kinetics, corrosion and thermodynamics have not been obtained due to the severe experimental condition. To get such data by experiments and computer simulations, a national program funded by Ministry of Education, Culture, Sports, Science and Technology (MEXT) has been started since December 2002. (author)

Stepwise Inquiry into Hard Water in a High School Chemistry Laboratory

Science.gov (United States)

Kakisako, Mami; Nishikawa, Kazuyuki; Nakano, Masayoshi; Harada, Kana S.; Tatsuoka, Tomoyuki; Koga, Nobuyoshi

2016-01-01

This study focuses on the design of a learning program to introduce complexometric titration as a method for determining water hardness in a high school chemistry laboratory. Students are introduced to the different properties and reactions of hard water in a stepwise manner so that they gain the necessary chemical knowledge and conceptual…

Surface chemistry and corrosion behavior of Inconel 625 and 718 in subcritical, supercritical, and ultrasupercritical water

Energy Technology Data Exchange (ETDEWEB)

Rodriguez, David; Merwin, Augustus; Karmiol, Zachary; Chidambaram, Dev, E-mail: dcc@unr.edu

2017-05-15

Highlights: • Mixtures of oxides containing Ni, Fe, Cr and Nb formed on the surface. • Short term exposure tests observed breakdown of native film. • Formation of a Fe rich oxide layer on Inconel 718 prevents mass loss. - Abstract: Corrosion behavior of Inconel 625 and 718 in subcritical, supercritical and ultrasupercritical water was studied as a function of temperature and time. The change in the chemistry of the as-received surface film on Inconel 625 and 718 after exposure to subcritical water at 325 °C and supercritical water at 425 °C and 527.5 °C for 2 h was studied. After exposure to 325 °C subcritical water, the CrO{sub 4}{sup 2−} based film formed; however minor quantities of NiFe{sub x}Cr{sub 2-x}O{sub 4} spinel compounds were observed. The oxide film formed on both alloys when exposed to supercritical water at 425 °C consisted of NiFe{sub x}Cr{sub 2-x}O{sub 4} spinel. The surface films on both alloys were identified as NiFe{sub 2}O{sub 4} when exposed to supercritical water at 527.5 °C. To characterize the fully developed oxide layer, studies were conducted at test solution temperatures of 527.5 and 600 °C. Samples were exposed to these temperatures for 24, 96, and 200 h. Surface chemistry was analyzed using X-ray diffraction, as well as Raman and X-ray photoelectron spectroscopies. Inconel 718 exhibited greater mass gain than Inconel 625 for all temperatures and exposure times. The differences in corrosion behavior of the two alloys are attributed to the lower content of chromium and increased iron content of Inconel 718 as compared to Inconel 625.

Surface chemistry and corrosion behavior of Inconel 625 and 718 in subcritical, supercritical, and ultrasupercritical water

International Nuclear Information System (INIS)

Rodriguez, David; Merwin, Augustus; Karmiol, Zachary; Chidambaram, Dev

2017-01-01

Highlights: • Mixtures of oxides containing Ni, Fe, Cr and Nb formed on the surface. • Short term exposure tests observed breakdown of native film. • Formation of a Fe rich oxide layer on Inconel 718 prevents mass loss. - Abstract: Corrosion behavior of Inconel 625 and 718 in subcritical, supercritical and ultrasupercritical water was studied as a function of temperature and time. The change in the chemistry of the as-received surface film on Inconel 625 and 718 after exposure to subcritical water at 325 °C and supercritical water at 425 °C and 527.5 °C for 2 h was studied. After exposure to 325 °C subcritical water, the CrO_4"2"− based film formed; however minor quantities of NiFe_xCr_2_-_xO_4 spinel compounds were observed. The oxide film formed on both alloys when exposed to supercritical water at 425 °C consisted of NiFe_xCr_2_-_xO_4 spinel. The surface films on both alloys were identified as NiFe_2O_4 when exposed to supercritical water at 527.5 °C. To characterize the fully developed oxide layer, studies were conducted at test solution temperatures of 527.5 and 600 °C. Samples were exposed to these temperatures for 24, 96, and 200 h. Surface chemistry was analyzed using X-ray diffraction, as well as Raman and X-ray photoelectron spectroscopies. Inconel 718 exhibited greater mass gain than Inconel 625 for all temperatures and exposure times. The differences in corrosion behavior of the two alloys are attributed to the lower content of chromium and increased iron content of Inconel 718 as compared to Inconel 625.

Road maps on research and development plans for water chemistry of nuclear power systems

International Nuclear Information System (INIS)

Uchida, Shunsuke; Katsumura, Yosuke; Fuse, Motomasa; Takamori, Kenro; Tsuchiuchi, Yoshihiro; Maeda, Noriyoshi

2008-01-01

Water chemistry of nuclear power plants has played an important role in reduction of personnel doses, structural materials and fuel integrity assurance, and reduction of radioactive wastes production. Further contributions are requested for advanced utilization of the LWR, advanced fuels and aging management of plants. Since water chemistry has an effect on all structure and materials immersed and at the same time affected by them, the optimum control not sticking to specific issues and covering the whole plant is required for these requests. Taking account of roles and activities of the industry, governmental institutes and academia, road maps on research and development plans for water chemistry were compiled into identified eleven items with targets and counter measures taken, such as common basic technologies, dose reduction, SCC mitigation, fuel cans corrosion/hydrogen absorption mitigation, condition based maintenance and flow accelerated corrosion mitigation. (T. Tanaka)

Development of Iridium Solid-state Reference Electrode for the Water Chemistry Status Measurement in Nuclear Power Plants

International Nuclear Information System (INIS)

Ku, Heekwon; Lim, Dongseok; Cho, Jaeseon

2013-01-01

The result of ECP measurement of piping material in nuclear power plant at low temperature using the developed iridium (SSRE) reference electrode is approximately -0.370V. Based on the various results of this study, the developed iridium (SSRE) reference electrode can be applied to the water chemistry environments of nuclear power plant. Various metallic materials used in a nuclear power plant have been exposed to a variety of water chemistry environments and the corrosion of metallic materials occurs due to the reactions between metal structures and water chemistry environments. Therefore, the management of the water chemistry factors is needed to prevent corrosion. The chemical factors affecting the corrosion are pH and Electrochemical Corrosion Potential (ECP). The world-wide studies suggest that ECP and pH are effective indicators for preventing the material damage from water chemistry condition. ECP and pH should be measured as the reference electrodes, and should show stable potential characteristics with fast responses. In this study, the iridium reference electrodes using a solid-state metal oxide electrode has been developed to measure effective indicators such as ECP and pH. The iridium (SSRE) reference electrode for the ECP measurement in water chemistry environment of nuclear power plants has been developed. A calibration for water chemistry measurement was performed by potential measurement of iridium (SSRE) reference electrode with Ag/AgCl (SSRE) reference electrode. The result exhibited a stable potential for 117 hours and a super-Nernst ian response with 63.12mV/p H. In this study, the iridium (SSRE) reference electrode shows super-Nernst ian characteristic and it may be caused by the property of electrolytically coated iridium oxide. Considering the long-term stability of the developed electrode, it is possible to apply as a reference electrode through calibration procedure

Substantial secondary organic aerosol formation in a coniferous forest: observations of both day- and nighttime chemistry

OpenAIRE

A. K. Y. Lee; J. P. D. Abbatt; W. R. Leaitch; S.-M. Li; S. J. Sjostedt; S. J. Sjostedt; J. J. B. Wentzell; J. Liggio; A. M. Macdonald

2016-01-01

Substantial biogenic secondary organic aerosol (BSOA) formation was investigated in a coniferous forest mountain region at Whistler, British Columbia. A largely biogenic aerosol growth episode was observed, providing a unique opportunity to investigate BSOA formation chemistry in a forested environment with limited influence from anthropogenic emissions. Positive matrix factorization of aerosol mass spectrometry (AMS) measurement identifie...

Methanol Formation via Oxygen Insertion Chemistry in Ices

Science.gov (United States)

Bergner, Jennifer B.; Öberg, Karin I.; Rajappan, Mahesh

2017-08-01

We present experimental constraints on the insertion of oxygen atoms into methane to form methanol in astrophysical ice analogs. In gas-phase and theoretical studies this process has previously been demonstrated to have a very low or nonexistent energy barrier, but the energetics and mechanisms have not yet been characterized in the solid state. We use a deuterium UV lamp filtered by a sapphire window to selectively dissociate O2 within a mixture of O2:CH4 and observe efficient production of CH3OH via O(1D) insertion. CH3OH growth curves are fit with a kinetic model, and we observe no temperature dependence of the reaction rate constant at temperatures below the oxygen desorption temperature of 25 K. Through an analysis of side products we determine the branching ratio of ice-phase oxygen insertion into CH4: ˜65% of insertions lead to CH3OH, with the remainder leading instead to H2CO formation. There is no evidence for CH3 or OH radical formation, indicating that the fragmentation is not an important channel and that insertions typically lead to increased chemical complexity. CH3OH formation from O2 and CH4 diluted in a CO-dominated ice similarly shows no temperature dependence, consistent with expectations that insertion proceeds with a small or nonexistent barrier. Oxygen insertion chemistry in ices should therefore be efficient under low-temperature ISM-like conditions and could provide an important channel to complex organic molecule formation on grain surfaces in cold interstellar regions such as cloud cores and protoplanetary disk midplanes.

Methanol Formation via Oxygen Insertion Chemistry in Ices

Energy Technology Data Exchange (ETDEWEB)

Bergner, Jennifer B. [Harvard University Department of Chemistry and Chemical Biology, 10 Oxford Street, Cambridge, MA 02138 (United States); Öberg, Karin I.; Rajappan, Mahesh [Harvard-Smithsonian Center for Astrophysics, 60 Garden Street, Cambridge, MA 02138 (United States)

2017-08-10

We present experimental constraints on the insertion of oxygen atoms into methane to form methanol in astrophysical ice analogs. In gas-phase and theoretical studies this process has previously been demonstrated to have a very low or nonexistent energy barrier, but the energetics and mechanisms have not yet been characterized in the solid state. We use a deuterium UV lamp filtered by a sapphire window to selectively dissociate O{sub 2} within a mixture of O{sub 2}:CH{sub 4} and observe efficient production of CH{sub 3}OH via O({sup 1}D) insertion. CH{sub 3}OH growth curves are fit with a kinetic model, and we observe no temperature dependence of the reaction rate constant at temperatures below the oxygen desorption temperature of 25 K. Through an analysis of side products we determine the branching ratio of ice-phase oxygen insertion into CH{sub 4}: ∼65% of insertions lead to CH{sub 3}OH, with the remainder leading instead to H{sub 2}CO formation. There is no evidence for CH{sub 3} or OH radical formation, indicating that the fragmentation is not an important channel and that insertions typically lead to increased chemical complexity. CH{sub 3}OH formation from O{sub 2} and CH{sub 4} diluted in a CO-dominated ice similarly shows no temperature dependence, consistent with expectations that insertion proceeds with a small or nonexistent barrier. Oxygen insertion chemistry in ices should therefore be efficient under low-temperature ISM-like conditions and could provide an important channel to complex organic molecule formation on grain surfaces in cold interstellar regions such as cloud cores and protoplanetary disk midplanes.

Discharge, sediment, and water chemistry in Clear Creek, western Nevada, water years 2013–16

Science.gov (United States)

Huntington, Jena M.; Riddle, Daniel J.; Paul, Angela P.

2018-05-01

Clear Creek is a small stream that drains the eastern Carson Range near Lake Tahoe, flows roughly parallel to the Highway 50 corridor, and discharges to the Carson River near Carson City, Nevada. Historical and ongoing development in the drainage basin is thought to be affecting Clear Creek and its sediment-transport characteristics. Previous studies from water years (WYs) 2004 to 2007 and from 2010 to 2012 evaluated discharge, selected water-quality parameters, and suspended-sediment concentrations, loads, and yields at three Clear Creek sampling sites. This report serves as a continuation of the data collection and analyses of the Clear Creek discharge regime and associated water-chemistry and sediment concentrations and loads during WYs 2013–16.Total annual sediment loads ranged from 870 to 5,300 tons during WYs 2004–07, from 320 to 1,770 tons during WYs 2010–12, and from 50 to 200 tons during WYs 2013–16. Ranges in annual loads during the three study periods were not significantly different; however, total loads were greater during 2004–07 than they were during 2013–16. Annual suspended-sediment loads in WYs 2013–16 showed no significant change since WYs 2010–12 at sites 1 (U.S. Geological Survey reference site 10310485; Clear Creek above Highway 50, near Spooner Summit, Nevada) or 2 (U.S. Geological Survey streamgage 10310500; Clear Creek above Highway 50, near Spooner Summit, Nevada), but significantly lower loads at site 3 (U.S. Geological Survey site 10310518; Clear Creek at Fuji Park, at Carson City, Nevada), supporting the theory of sediment deposition between sites 2 and 3 where the stream gradient becomes more gradual. Currently, a threshold discharge of about 3.3 cubic feet per second is required to mobilize streambed sediment (bedload) from site 2 in Clear Creek. Mean daily discharge was significantly lower in 2010–12 than in 2004–07 and also significantly lower in 2013–16 than in 2010–12. During this study, lower bedload, and

Actinide/crown ether chemistry

International Nuclear Information System (INIS)

Benning, M.M.

1988-01-01

A structural survey of actinide/crown ether compounds was conducted in order to investigate the solid state chemistry of these complexes. Several parameters - the metal size, crown type, counterion, solvent systems and reaction and crystallization conditions - were varied to correlate their importance in complexation. Under atmospheric conditions, two types of complexes were isolated, those containing only hydrogen-bonded crown interactions and instances where the crown interacts directly with the metal center. In both cases, water seems to play a very important role. When coordinated to the metal, water molecules exhibit the necessary donor properties required for the formation of hydrogen-bonded contacts. The water molecules also provide fierce competition with the crown ethers for metal-binding sites and in most cases prohibit the formation of complexes in which direct metal-ligand association exists. The results of this study indicate that direct interaction between the metal atoms and the crown ethers, in the presence of water, can only occur with polyether conformations which limit the steric replusions within the metal coordination sphere

Dictionary of water chemistry. English/German/French. Woerterbuch der Wasserchemie. Deutsch/Englisch/Franzoesisch

Energy Technology Data Exchange (ETDEWEB)

Ammon, F von

1985-01-01

This dictionary presents a compilation of the most important terms related to water composition and quality. Technical terms used to describe water purification and other technical processes are also included. In fact, terms come from all areas of water chemistry: they concern water sampling, water analysis and its statistical interpretation, the evalutation of results as indicators for planing and operating water purification and waste-water plants.

Ammonia role in WWER primary circuit water chemistry optimization

International Nuclear Information System (INIS)

Kritskij, V.G.; Stjagkin, P.S.; Chvedova, M.N.; Slobodov, A.A.

1999-01-01

Ammonia influence on iron crud's solubility at 300 deg. C and different relations of boric acid and alkaline cation sum are considered. Reduction of dose rate on WWER-440 steam generators at average ammonia concentration increasing is empirically explained. Practical recommendations on optimization of WWER primary circuit water chemistry are given. (author)

The chemistry of water reactor fuel

International Nuclear Information System (INIS)

Potter, P.E.

1990-01-01

In this paper, the authors discuss features of the changes in chemical constitution which occur in fuel and fuel rods for water reactors during operation and in fault conditions. The fuel for water reactors consists of pellets of urania (UO 2 ) clad in Zircaloy. An essential step in the prediction of the fate of all the radionuclides in a fault or accident is to possess a detailed knowledge of their chemical behavior at all stages of the development of such incidents. In this paper, the authors consider: the chemical constitution of fuel during operation at temperatures corresponding to rather low ratings, together with a quite detailed discussion of the chemistry within the fuel-clad gap; the behavior of fuel subjected to higher temperatures and ratings than those of contemporary fuel; and the changes in constitution on failure of fuel rods in fault or accident conditions

High temperature on-line monitoring of water chemistry and corrosion control in water cooled power reactors. Report of a co-ordinated research project 1995-1999

International Nuclear Information System (INIS)

2002-07-01

This report documents the results of the Co-ordinated Research Project (CRP) on High Temperature On-line Monitoring of Water Chemistry and Corrosion in Water Cooled Power Reactors (1995-1999). This report attempts to provide both an overview of the state of the art with regard to on-line monitoring of water chemistry and corrosion in operating reactors, and technical details of the important contributions made by programme participants to the development and qualification of new monitoring techniques. The WACOL CRP is a follow-up to the WACOLIN (Investigations on Water Chemistry Control and Coolant Interaction with Fuel and Primary Circuit Materials in Water Cooled Power Reactors) CRP conducted by the IAEA from 1986 to 1991. The WACOLIN CRP, which described chemistry, corrosion and activity-transport aspects, clearly showed the influence of water chemistry on corrosion of both fuel and reactor primary-circuit components, as well as on radiation fields. It was concluded that there was a fundamental need to monitor water-chemistry parameters in real time, reliably and accurately. The objectives of the WACOL CRP were to establish recommendations for the development, qualification and plant implementation of methods and equipment for on-line monitoring of water chemistry and corrosion. Chief investigators from 18 organizations representing 15 countries provided a variety of contributions aimed at introducing proven monitoring techniques into plants on a regular basis and filling the gaps between plant operator needs and available monitoring techniques. The CRP firmly demonstrated that in situ monitoring is able to provide additional and valuable information to plant operators, e.g. ECP, high temperature pH and conductivity. Such data can be obtained promptly, i.e. in real time and with a high degree of accuracy. Reliable techniques and sensor devices are available which enable plant operators to obtain additional information on the response of structural materials in

Water-rock interaction and chemistry of groundwaters from the Canadian Shield

International Nuclear Information System (INIS)

Frape, S.K.; Fritz, P.; McNutt, R.H.

1984-01-01

The chemical and isotopic compositions of groundwaters in the crystalline rocks of the Canadian Shield reflect different degrees of rock-water interactions. The chemistry of the shallow, geochemically immature ground waters and especially of the major cations is controlled by local rock compositions, whereby dissolution reactions dominate. Conservative constituents, such as chloride and bromide, however, are not entirely a result of such reactions but appear to be readily added from leachable salts during the initial stages of the geochemical evolution of these waters. Their concentration changes little as major cations increase, until concentrations of Total Dissolved Solids (TDS) reach 3000 to 5000 mg l -1 . The isotopic composition of these shallow waters reflects local, present day precipitations. In contrast to the shallow groundwaters, the isotopic and chemical compositions of the deep, saline waters and brines are determined by extensive, low-temperature rock-water interactions. This is documented in major ion chemistries, 18 O contents and strontium isotopic compositions. These data indicate that the deep brines have been contained in hydrologically isolated pockets. The almost total loss of primary compositions make discussions on the origin of these brines very speculative. However, all brines from across the Canadian Shield have a very similar chemical composition, which probably reflects a common geochemical history. (author)

Effect of water chemistry on corrosion of stainless steel and deposition of corrosion products in high temperature pressurised water

International Nuclear Information System (INIS)

Morrison, Jonathan; Cooper, Christopher; Ponton, Clive; Connolly, Brian; Banks, Andrew

2012-09-01

temperatures between 200 and 300 deg. C. Finally, it has been recognised that there is an electrokinetic component to the deposition occurring within flow restrictions, but very few investigations have been performed to study the electrokinetic behaviour at a geometric flow restriction. Work that has been previously attempted has focused on electrokinetics of crud deposition in the secondary side water chemistry. This electrokinetic behaviour, manifested as a streaming current, is believed to be influential in the electrochemical reactions occurring at flow restrictions resulting in the formation of the observed crud deposits. As part of this programme a high velocity (up to 30 ms -1 ) flow rate loop operating at high temperature (up to 315 deg. C) and pressure (up to 150 bar) has been constructed to study the deposition of material at a flow restriction of known geometry under simulated primary side water chemistry, temperature and pressure conditions. Furthermore, to assist in the understanding of measured streaming currents present as a function of desired geometries, preliminary experiments utilising a second 'cold' loop will be performed, where water of up to 373 K will be flowed at high velocity through an instrumented sample section. (authors)

Effects of using presentation formats that accommodate the learner's multiple intelligences on the learning of freshman college chemistry concepts

Science.gov (United States)

Brown Wright, Gloria Aileen

Howard Gardner's Theory of Multiple Intelligences identifies linguistic, spatial and logical-mathematical intelligences as necessary for learning in the physical sciences. He has identified nine intelligences which all persons possess to varying degrees, and says that learning is most effective when learners receive information in formats that correspond to their intelligence strengths. This research investigated the importance of the multiple intelligences of students in first-year college chemistry to the learning of chemistry concepts. At three pre-selected intervals during the first-semester course each participant received a tutorial on a chemistry topic, each time in a format corresponding to a different one of the three intelligences, just before the concept was introduced by the class lecturer. At the end of the experiment all subjects had experienced each of the three topics once and each format once, after which they were administered a validated instrument to measure their relative strengths in these three intelligences. The difference between a pre- and post-tutorial quiz administered on each occasion was used as a measure of learning. Most subjects were found to have similar strengths in the three intelligences and to benefit from the tutorials regardless of format. Where a difference in the extent of benefit occurred the difference was related to the chemistry concept. Data which indicate that students' preferences support these findings are also included and recommendations for extending this research to other intelligences are made.

Water chemistry in PWR

International Nuclear Information System (INIS)

Abe, Kenji

1987-01-01

This article outlines major features and basic concept of the secondary system of PWR's and water properties control measures adopted in recent PWR plants. The secondary system of a PWR consists of a condenser cooling pipe (aluminum-brass, titanium, or stainless steel), low-pressure make-up water heating pipe (aluminum-brass or stainless steel), high-ressure make-up water heating pipe (cupro-nickel or stainless steel), steam generator heat-transfer pipe (Inconel 600 or 690), and bleed/drain pipe (carbon steel, low alloy steel or stainless steel). Other major pipes and equipment are made of carbon steel or stainless steel. Major troubles likely to be caused by water in the secondary system include reduction in wall thickness of the heat-transfer pipe, stress corrosion cracking in the heat-transfer pipe, and denting. All of these are caused by local corrosion due to concentration of purities contained in water. For controlling the water properties in the secondary system, it is necessary to prevent impurities from entering the system, to remove impurities and corrosion products from the system, and to prevent corrosion of apparatus making up the system. Measures widely adopted for controlling the formation of IGA include the addition of boric acid for decreasing the concentration of free alkali and high hydrazine operation for providing a highly reducing atmospere. (Nogami, K.)

Substantial secondary organic aerosol formation in a coniferous forest: observations of both day- and nighttime chemistry

Directory of Open Access Journals (Sweden)

A. K. Y. Lee

2016-06-01

Full Text Available Substantial biogenic secondary organic aerosol (BSOA formation was investigated in a coniferous forest mountain region in Whistler, British Columbia. A largely biogenic aerosol growth episode was observed, providing a unique opportunity to investigate BSOA formation chemistry in a forested environment with limited influence from anthropogenic emissions. Positive matrix factorization of aerosol mass spectrometry (AMS measurement identified two types of BSOA (BSOA-1 and BSOA-2, which were primarily generated by gas-phase oxidation of monoterpenes and perhaps sesquiterpenes. The temporal variations of BSOA-1 and BSOA-2 can be explained by gas–particle partitioning in response to ambient temperature and the relative importance of different oxidation mechanisms between day and night. While BSOA-1 arises from gas-phase ozonolysis and nitrate radical chemistry at night, BSOA-2 is likely less volatile than BSOA-1 and consists of products formed via gas-phase oxidation by OH radical and ozone during the day. Organic nitrates produced through nitrate radical chemistry can account for 22–33 % of BSOA-1 mass at night. The mass spectra of BSOA-1 and BSOA-2 have higher values of the mass fraction of m/z 91 (f91 compared to the background organic aerosol. Using f91 to evaluate BSOA formation pathways in this unpolluted, forested region, heterogeneous oxidation of BSOA-1 is a minor production pathway of BSOA-2.

Measuring restoration progress using pore- and surface-water chemistry across a chronosequence of formerly afforested blanket bogs.

Science.gov (United States)

Gaffney, Paul P J; Hancock, Mark H; Taggart, Mark A; Andersen, Roxane

2018-08-01

During the restoration of degraded bogs and other peatlands, both habitat and functional recovery can be closely linked with nutrient cycling, which is reflected in pore- and surface-water chemistry. Several peatland restoration studies have shown that the time required for recovery of target conditions is slow (>10 years); for heavily-impacted, drained and afforested peatlands of northern Scotland, recovery time is unknown. We monitored pore- and surface-water chemistry across a chronosequence of formerly drained, afforested bog restoration sites spanning 0-17 years, using a space-for-time substitution, and compared them with open blanket bog control sites. Our aims were to measure rate of recovery towards bog conditions and to identify the best suite of water chemistry variables to indicate recovery. Our results show progress in recovery towards bog conditions over a 0-17 year period post-restoration. Elements scavenged by trees (Mg, Na, S) completely recovered within that period. Many water chemistry variables were affected by the restoration process itself, but recovered within 11 years, except ammonium (NH 4 + ), Zn and dissolved organic carbon (DOC) which remained elevated (when compared to control bogs) 17 years post restoration. Other variables did not completely recover (water table depth (WTD), pH), exhibiting what we term "legacy" effects of drainage and afforestation. Excess N and a lowered WTD are likely to slow the recovery of bog vegetation including key bog plants such as Sphagnum mosses. Over 17 years, we measured near-complete recovery in the chemistry of surface-water and deep pore-water but limited progress in shallow pore-water. Our results suggest that at least >17 years are required for complete recovery of water chemistry to bog conditions. However, we expect that newer restoration methods including conifer harvesting (stem plus brash) and the blocking of plough furrows (to increase the WTD) are likely to accelerate the restoration process

Effects of iron on arsenic speciation and redox chemistry in acid mine water

Science.gov (United States)

Bednar, A.J.; Garbarino, J.R.; Ranville, J.F.; Wildeman, T.R.

2005-01-01

Concern about arsenic is increasing throughout the world, including areas of the United States. Elevated levels of arsenic above current drinking-water regulations in ground and surface water can be the result of purely natural phenomena, but often are due to anthropogenic activities, such as mining and agriculture. The current study correlates arsenic speciation in acid mine drainage and mining-influenced water with the important water-chemistry properties Eh, pH, and iron(III) concentration. The results show that arsenic speciation is generally in equilibrium with iron chemistry in low pH AMD, which is often not the case in other natural-water matrices. High pH mine waters and groundwater do not always hold to the redox predictions as well as low pH AMD samples. The oxidation and precipitation of oxyhydroxides deplete iron from some systems, and also affect arsenite and arsenate concentrations through sorption processes. ?? 2004 Elsevier B.V. All rights reserved.

Chemistry of cost effective water treatment programme in HWP (Manuguru)

International Nuclear Information System (INIS)

Mohapatra, C.; Laxmana Prasad, K.

2008-01-01

In order to develop a water treatment programme following points must be kept in mind: Effectiveness to achieve desired water quality objectives; Compliance with regulatory requirements; Cost minimization; Safety; Easy operation and protection to equipments. Heavy Water Plant (Manuguru) laboratory has developed treatment programs to treat raw water and cooling water which satisfy the above requirements and has been in use for last several years successfully without any problem. These treatment programs have been given to other plants in Heavy Water Board for implementation. This paper describes the chemistry of the treatment program and cost minimization achieved. Further these treatments have helped the plant in achieving ΦZero Discharge and indirectly reduced the production cost. The chemistry parameters are monitored regularly to ascertain the effectiveness of these treatments. The areas where significant benefits derived are raw water treatment using polyelectrolyte instead of inorganic coagulant (alum), change over of regenerant of cation exchangers from hydrochloric acid to sulfuric acid and development of in-house cooling water treatment formulation. The advantages and cost effectiveness of these treatments are discussed in detail. Further these treatments helped the plant in achieving Zero discharge and indirectly reduced production cost of heavy water. The dosage of 3 ppm of polyelectrolyte can replace 90 ppm alum at turbidity level of 300 NTU of raw water which has resulted in cost saving of Rs. 15 - 20 Lakhs in a year besides other advantages. The changeover of regenerant from HCl to H 2 SO 4 will result in cost saving of at least Rs. 1.4 Crore a year along with other advantages. The change over of proprietary formulation to in-house formulation in cooling water treatment has resulted a saving about Rs. 11 Lakhs a year. To achieve the above objectives in a sustainable way the performance results are being monitored (author)

Fog water chemistry in the Namib desert, Namibia

Science.gov (United States)

Eckardt, Frank D.; Schemenauer, Robert S.

This study documents the ion concentrations and ion enrichment relative to sea water, in Namib Desert fog water, with the purpose of establishing its suitability for future fogwater collection schemes, while also examining claims that Namib Desert fog water carries exceptionally high concentrations of sulphate, which may be responsible for the formation of gypsum deposits in the desert. The work suggests that Namibian fog water is at least as clean as has been reported from other coastal deserts in South America and Arabia, and provides a source of very clean water for the coastal desert region of south-western Africa. It does not appear that fog is an efficient sulphur source for the formation of the gypsum deposits, unless rare events with high concentrations of marine sulphur compounds occur.

Flow Accelerated Corrosion: Effect of Water Chemistry and Database Construction

Energy Technology Data Exchange (ETDEWEB)

Lee, Eun Hee; Kim, Kyung Mo; Lee, Gyeong Geun; Kim, Dong Jin [KAERI, Daejeon (Korea, Republic of)

2016-05-15

Flow accelerated corrosion (FAC) of carbon steel piping in pressurized water reactors (PWRs) has been a major issue in nuclear industry. Severe accidents at Surry Unit 2 in 1986 and Mihama Unit 3 in 2004 initiated the world wide interest in this area. FAC is a dissolution process of the protective oxide layer on carbon steel or low-alloy steel when these parts are exposed to flowing water (single-phase) or wet steam (two-phase). In a single-phase flow, a scalloped, wavy, or orange peel and in a two-phase flow, tiger striping is observed, respectively. FAC is affected by many parameters, like material composition, pH, dissolved oxygen (DO), flow velocity, system pressure, and steam quality. This paper describes the water chemistry factors influencing on FAC and the database is then constructed using literature data. In order to minimize FAC in NPPs, the optimal method is to control water chemistry parameters. However, quantitative data about FAC have not been published for proprietary reason even though qualitative behaviors of FAC have been well understood. A database was constructed using experimental data in literature. Accurate statistical analysis will be performed using this database to identify the relationship between the FAC rate and test environment.

DOE fundamentals handbook: Chemistry

International Nuclear Information System (INIS)

1993-01-01

This handbook was developed to assist nuclear facility operating contractors in providing operators, maintenance personnel, and the technical staff with the necessary fundamentals training to ensure a basic understanding of chemistry. This volume contains the following modules: reactor water chemistry (effects of radiation on water chemistry, chemistry parameters), principles of water treatment (purpose; treatment processes [ion exchange]; dissolved gases, suspended solids, and pH control; water purity), and hazards of chemicals and gases (corrosives [acids, alkalies], toxic compounds, compressed gases, flammable/combustible liquids)

["Chemistry of Concepts”and “Historical Sense”. On Philosophical Concept Formation].

Science.gov (United States)

Blättler, Christine

2015-06-01

"Chemistry of Concepts" and "Historical Sense". On Philosophical Concept Formation. The question concerning concepts and their relations to objects and words has had a long and controversial history. Recently, it is challenged by an anew turn towards objects and an emphasized object-oriented ontology. The article argues that one reason for this is the reduction of concepts towards pure rational constructions and offers arguments for alternative understandings. In this context, the article proposes a re-reading of Nietzsche's particular approach and shows that Nietzsche's thought is decisively shaped by the sciences of his time, especially physiology and chemistry. Before the background of the recent increase in research interest on Nietzsche and the sciences the article examines place and function of the sciences related to the genealogy and justification of concepts. Opposing a strong naturalist reading it makes a plea for understanding Nietzsche's epistemological critique concerning concepts systematically as a triple one: philological, physiological, and historical. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Variance in water chemistry parameters in isolated wetlands of Florida, USA, and relationships with macroinvertebrate and diatom community structure

Science.gov (United States)

Eighty small isolated wetlands throughout Florida were sampled in 2005 to explore within-site variability of water chemistry parameters and relate water chemistry to macroinvertebrate and diatom community structure. Three samples or measures of water were collected within each si...

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

Chemistry teacher initial formation under the eye of the coordinators of the courses

Directory of Open Access Journals (Sweden)

Roberta Guimarães Corrêa

2016-05-01

Full Text Available Despite the recognition of the need for change and the constant production of studies on initial formation, the degree courses still have questions that need to be discussed. These issues are related to the difficulty to overcome the lack of teachers in basic education and the type of formation offered in undergraduate courses, which does not seem to meet the current Brazilian educational demands. This paper presents data from a qualitative study conducted with coordinators of seven higher education institutions in the state of São Paulo. Despite the different institutional realities presented in this work, the difficulty of effectively contribute to the formation of chemistry teachers is common to all the institutions. Lack of interest in initial formation teacher’s courses, evasion problems, relationship between the initial formation of chemical teachers and chemistry’s professionals and the lack of commitment of teachers marked the reports of the coordinators of the courses.

Covalent-Bond Formation via On-Surface Chemistry.

Science.gov (United States)

Held, Philipp Alexander; Fuchs, Harald; Studer, Armido

2017-05-02

In this Review article pioneering work and recent achievements in the emerging research area of on-surface chemistry is discussed. On-surface chemistry, sometimes also called two-dimensional chemistry, shows great potential for bottom-up preparation of defined nanostructures. In contrast to traditional organic synthesis, where reactions are generally conducted in well-defined reaction flasks in solution, on-surface chemistry is performed in the cavity of a scanning probe microscope on a metal crystal under ultrahigh vacuum conditions. The metal first acts as a platform for self-assembly of the organic building blocks and in many cases it also acts as a catalyst for the given chemical transformation. Products and hence success of the reaction are directly analyzed by scanning probe microscopy. This Review provides a general overview of this chemistry highlighting advantages and disadvantages as compared to traditional reaction setups. The second part of the Review then focuses on reactions that have been successfully conducted as on-surface processes. On-surface Ullmann and Glaser couplings are addressed. In addition, cyclodehydrogenation reactions and cycloadditions are discussed and reactions involving the carbonyl functionality are highlighted. Finally, the first examples of sequential on-surface chemistry are considered in which two different functionalities are chemoselectively addressed. The Review gives an overview for experts working in the area but also offers a starting point to non-experts to enter into this exciting new interdisciplinary research field. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Relationships between precipitation and surface water chemistry in three Carolina bays

International Nuclear Information System (INIS)

Monegue, R.L.; Jagoe, C.H.

1995-01-01

Carolina Bays are shallow freshwater wetlands, the only naturally occurring lentic systems on the southeastern coastal plain. Bays are breeding sites for many amphibian species, but data on precipitation/surface water relationships and long-term chemical trends are lacking. Such data are essential to interpret major fluctuations in amphibian populations. Surface water and bulk precipitation were sampled bi-weekly for over two years at three bays along a 25 km transect on the Savannah River Site in South Carolina. Precipitation chemistry was similar at all sites; average pH was 4.56, and the major ions were H + (30.8 % of total), and SO 4 (50.3% of total). H + was positively correlated with SO 4 , suggesting the importance of anthropogenic acids to precipitation chemistry. All three bays, Rainbow Bay (RB), Thunder Bay (TB), and Ellenton Bay (EB), contained soft (specific conductivity 5--90 microS/cm), acidic water (pH 4.0--5.9) with DOM from 4--40 mg/L. The major cation for RB, TB, and EB, respectively, was: Mg (30.8 % of total); Na (27% of total); and Ca (34.2% of total). DOM was the major anion for all bays, and SO 4 represented 13 to 28 % of total anions. H + was not correlated to DOM or SO, in RB; H + was positively correlated to DOM and SO 4 in TB, and negatively correlated to DOM and SO 4 in EB. Different biogeochemical processes probably control pH and other chemical variables in each bay. While surface water H + was not directly correlated with precipitation H + , NO 3 , or SO 4 , precipitation and shallow groundwater are dominant water sources for these bays. Atmospheric inputs of anthropogenic acids and other chemicals are important factors influencing bay chemistry

Experimental and numerical study of deposit formation in secondary side SG TSP by electrokinetic approach

International Nuclear Information System (INIS)

Guillodo, Michael; Foucault, Marc; Ryckelynck, Natacha; Chahma, Farah; Guingo, Mathieu; Mansour, Carine; Alos-Ramos, Olga; Corredera, Geraldine

2012-09-01

Corrosion products deposit formation observed in PWR steam generators (SGs) - related to SG free span fouling and SG clogging - is now reported since several years. SG clogging is a localized phenomenon observed between the leading edge of the Tube Support Plate (TSP) and SG tubing materials. Based on visual inspections, it was found that the gaps between SG tubing material and TSP at the lower part of the broached holes were getting progressively blocked. Therefore, for safe operation, most affected PWRs had to be operated at reduced power. TSP blockage was mainly observed for low-pH water chemistry conditioning, which directly depends on the operating water chemistry. The TSP blockage mechanism is complex due to the localized conditions in which flow pattern change, chemistry and electrochemical conditions are not well understood. Electrokinetic considerations could be pointed out to explain the coupling of chemistry, materials and thermohydraulic (T/H) conditions. In this frame AREVA and EDF have launched a long-term R and D program in order to understand the mechanisms driving the formation of SG clogging. This study based on parametric laboratory tests aims to assess the role of secondary water chemistry, material and T/H conditions on deposit formation. The experimental approach focused on electrokinetic measurements of metallic substrates and on the assessment of oxidation properties of materials in secondary side chemistry. An overall analysis of recent results is presented to address SG deposit formation in secondary water chemistry for various conditioning amines - morpholine, ethanolamine and dimethylamine. To complete the study, the experimental results have been correlated to CFD simulations of particle deposition, by means of stochastic Lagrangian models. These calculations have in particular reproduced correctly the location of the most important particle deposit (the leading edge of the test tube), and have stressed the influence of the

Effect of water chemistry improvement on flow accelerated corrosion in light-water nuclear reactor

International Nuclear Information System (INIS)

Sugino, Wataru; Ohira, Taku; Nagata, Nobuaki; Abe, Ayumi; Takiguchi, Hideki

2009-01-01

Flow Accelerated Corrosion (FAC) of Carbon Steel (CS) piping has been one of main issues in Light-Water Nuclear Reactor (LWRs). Wall thinning of CS piping due to FAC increases potential risk of pipe rupture and cost for inspection and replacement of damaged pipes. In particular, corrosion products generated by FAC of CS piping brought steam generator (SG) tube corrosion and degradation of thermal performance, when it intruded and accumulated in secondary side of PWR. To preserve SG integrity by suppressing the corrosion of CS, High-AVT chemistry (Feedwater pH9.8±0.2) has been adopted to Tsuruga-2 (1160 MWe PWR, commercial operation in 1987) in July 2005 instead of conventional Low-AVT chemistry (Feedwater pH 9.3). By the High-AVT adoption, the accumulation rate of iron in SG was reduced to one-quarter of that under conventional Low-AVT. As a result, a tendency to degradation of the SG thermal efficiency was improved. On the other hand, it was clarified that High-AVT is ineffective against Flow Accelerated Corrosion (FAC) at the region where the flow turbulence is much larger. By contrast, wall thinning of CS feed water pipes due to FAC has been successfully controlled by oxygen treatment (OT) for long time in BWRs. Because Magnetite film formed on CS surface under AVT chemistry has higher solubility and porosity in comparison with Hematite film, which is formed under OT. In this paper, behavior of the FAC under various pH and dissolved oxygen concentration are discussed based on the actual wall thinning rate of BWR and PWR plant and experimental results by FAC test-loop. And, it is clarified that the FAC is suppressed even under extremely low DO concentration such as 2ppb under AVT condition in PWR. Based on this result, we propose the oxygenated water chemistry (OWC) for PWR secondary system which can mitigate the FAC of CS piping without any adverse effect for the SG integrity. Furthermore, the applicability and effectiveness of this concept developed for FAC

Steam Generator Owners Group PWR secondary water chemistry guidelines

International Nuclear Information System (INIS)

Welty, C.S. Jr.; Green, S.J.

1985-01-01

In 1981 the Steam Generator Owners Group (SGOG), a group of domestic and foreign pressurized water reactor (PWR) owners, developed and issued the PWR secondary water chemistry guidelines. The guidelines were prepared in response to the growing recognition that a majority of the problems causing reduced steam generator reliability (e.g., denting, wasteage, pitting, etc.) were related to secondary (steam) side water purity. The guidelines were subsequently issued as an Electric Power Research Institute (EPRI) report. In 1984 they were revised to reflect industry experience in adopting the original issuance and to incorporate new information on causes of corrosion damage. The guidelines have been endorsed and their adoption recommended by the SGOG

IAEA programme on water chemistry in nuclear power plants

International Nuclear Information System (INIS)

Nechaev, A.F.; Skjoeldebrand, R.

1988-01-01

The paper reviews the past future efforts of the IAEA, directed to ensure optimal water chemistry regimes in nuclear power plants. Corrosion of structural materials resulting from the interaction of the coolant with the internal surfaces comprising the primary heat transfer and auxiliary circuits of water reactors, creates two main problems. The first is an operational problem resulting in an increase in the core pressure drop or overheating of the fuel elements induced by crud buildup on the fuel cladding. The second problem is related to occupational radiation exposures arising from contamination of out-of-flux surfaces by corrosion products activated in the reactor core. These are the problems of reliability and safety which together with economics could be considered as the 'three whales' of nuclear power. The main goals of international cooperation in reactor water chemistry are: (1) to create a balanced and well-grounded methodological basis for corresponding regulatory and engineering solutions on a national level and (2) to improve 'the models and predictive capability of specialists for conditions that are different from or perhaps just beyond the realm of experience'. Continuing efforts are required to guarantee the highest reliability and safety standards under favorable economic indices of nuclear power plants, and to obtain understanding of such significant potential for solving the remaining problems. (Nogami, K.)

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…

Variability in chemistry of surface and soil waters of an ...

African Journals Online (AJOL)

2017-01-01

Jan 1, 2017 ... processing in the Okavango Delta, Botswana. Keotshephile ... 4Climate System Analysis Group, University of Cape Town, South Africa ... input and final fate of solutes is of critical ecological importance ... a wetland system therefore requires an in-depth understanding of the water chemistry of that system.

Chemistry in water reactors: operating experience and new developments. 2 volumes

International Nuclear Information System (INIS)

1994-01-01

These proceedings of the International conference on chemistry in water reactors (Operating experience and new developments), Volume 1, are divided into 8 sessions bearing on: (session 1) Primary coolant activity, corrosion products (5 conferences), (session 2) Dose reduction (4 conferences), (session 3) New developments (4 conferences), poster session: Primary coolant chemistry (16 posters), (session 4) Decontamination (5 conferences), poster session (2 posters), (session 5) BWR-Operating experience (3 conferences), (session 6) BWR-Modelling of operating experience (4 conferences), (session 7) BWR-Basic studies (4 conferences), (session 8) BWR-New technologies (3 conferences)

Identifying and Remediating High Water Production Problems in Basin-Centered Formations

Energy Technology Data Exchange (ETDEWEB)

R.L. Billingsley

2005-12-01

Through geochemical analyses of produced waters, petrophysics, and reservoir simulation we developed concepts and approaches for mitigating unwanted water production in tight gas reservoirs and for increasing recovery of gas resources presently considered noncommercial. Only new completion research (outside the scope of this study) will validate our hypothesis. The first task was assembling and interpreting a robust regional database of historical produced-water analyses to address the production of excessive water in basin-centered tight gas fields in the Greater Green (GGRB ) and Wind River basins (WRB), Wyoming. The database is supplemented with a sampling program in currently active areas. Interpretation of the regional water chemistry data indicates most produced waters reflect their original depositional environments and helps identify local anomalies related to basement faulting. After the assembly and evaluation phases of this project, we generated a working model of tight formation reservoir development, based on the regional nature and occurrence of the formation waters. Through an integrative approach to numerous existing reservoir concepts, we synthesized a generalized development scheme organized around reservoir confining stress cycles. This single overarching scheme accommodates a spectrum of outcomes from the GGRB and Wind River basins. Burial and tectonic processes destroy much of the depositional intergranular fabric of the reservoir, generate gas, and create a rock volume marked by extremely low permeabilities to gas and fluids. Stress release associated with uplift regenerates reservoir permeability through the development of a penetrative grain bounding natural fracture fabric. Reservoir mineral composition, magnitude of the stress cycle and local tectonics govern the degree, scale and exact mechanism of permeability development. We applied the reservoir working model to an area of perceived anomalous water production. Detailed water analyses

Kiche: A simulation tool for kinetics of iodine chemistry in the containment of light water reactors under severe accident conditions (Contract research)

International Nuclear Information System (INIS)

Moriyama, Kiyofumi; Maruyama, Yu; Nakamura, Hideo

2011-03-01

An iodine chemistry simulation tool, Kiche, was developed for analyses of chemical kinetics relevant to iodine volatilization in the containment vessel of light water reactors (LWRs) during a severe accident. It consists of a Fortran code to solve chemical kinetics models, reaction databases written in plain text format, and peripheral tools to convert the reaction databases into Fortran codes to solve corresponding ordinary differential equation sets. Potential advantages of Kiche are the text format reaction database separated from the code that provides flexibility of the chemistry model, and, being a Fortran code which is relatively easily coupled with other Fortran codes such as severe accident analysis codes. This document describes the model, solution method, code structure, and examples of application of Kiche for simulation of experiments. The calculation results by the present model agreed well with the experimental data and it indicates the model properly includes the most important processes in the volatilization of iodine from irradiated iodide solutions with or without organic impurities. The appendixes give practical information for the usage of Kiche. (author)

On-line water chemistry monitoring for corrosion prevention in ageing nuclear power plants

International Nuclear Information System (INIS)

Aaltonen, P.; Jaernstroem, R.; Kvarnstroem, R.; Chanfreau, E.

1991-01-01

General corrosion and consequently radiation buildup in nuclear power plants are controlled by the selection of material and the chemical environment. In power plants useful information concerning the kinetics of chemical reactions can be obtained by using high temperature, high pressure measurements for pH, conductivity and electrochemical potentials (ECP) of construction materials or redox-potential. The rates of general or uniform corrosion of materials in contact with the primary coolant are quite low and do not compromise the integrity of the primary circuit. Chemistry control should be applied in the first hand to minimize the dissolution and the transport and subsequent deposition of activated corrosion products to out-of-core regions. A computerized monitoring system for high temperature high pressure pH and electrochemical potential (ECP) has been in continuous use at the Loviisa power plant since 1988. Special emphasis has been put on learning the effect of pH and ECP control during cooldown process in order to further reduce background radiation buildup. During the shutdown for refueling outage in summer 1989 the high temperature water chemistry parameters were monitored. In addition to the high temperature water chemistry parameters concentrations of dissolved corrosion products as well as the activities of the corrosion products were measured. In this paper the results obtained through simultaneous monitoring of water chemistry parameters and concentrations of dissolved corrosion products as well as the activity measurements are presented and discussed. (author)

Disinfection by-product formation of UV treated swimming pool water

DEFF Research Database (Denmark)

Spiliotopoulou, Aikaterini; Hansen, Kamilla Marie Speht; Andersen, Henrik Rasmus

2015-01-01

Water samples from 3 indoor swimming pool facilities were tested to evaluate UV-induced effects on swimming pool water chemistry. Concentration change of several DBPs was investigated in experiments including medium pressure UV treatment with and without chlorine and post-UV chlorination. Post-UV...

A Water Chemistry Perspective on Flowback Reuse with Several Case Studies, March 30, 2011

Science.gov (United States)

This presentation discusses the reuse of frac flowback from a water chemistry perspective. Two examples of flowback reuse, where a minimal water treatment has been used, describe the rationale for why the practice is considered acceptable.

In-Package Chemistry Abstraction

Energy Technology Data Exchange (ETDEWEB)

P.S. Domski

2003-07-21

The work associated with the development of this model report was performed in accordance with the requirements established in ''Technical Work Plan for Waste Form Degradation Modeling, Testing, and Analyses in Support of SR and LA'' (BSC 2002a). The in-package chemistry model and in-package chemistry model abstraction are developed to predict the bulk chemistry inside of a failed waste package and to provide simplified expressions of that chemistry. The purpose of this work is to provide the abstraction model to the Performance Assessment Project and the Waste Form Department for development of geochemical models of the waste package interior. The scope of this model report is to describe the development and validation of the in-package chemistry model and in-package chemistry model abstraction. The in-package chemistry model will consider chemical interactions of water with the waste package materials and the waste form for commercial spent nuclear fuel (CSNF) and codisposed high-level waste glass (HLWG) and N Reactor spent fuel (CDNR). The in-package chemistry model includes two sub-models, the first a water vapor condensation (WVC) model, where water enters a waste package as vapor and forms a film on the waste package components with subsequent film reactions with the waste package materials and waste form--this is a no-flow model, the reacted fluids do not exit the waste package via advection. The second sub-model of the in-package chemistry model is the seepage dripping model (SDM), where water, water that may have seeped into the repository from the surrounding rock, enters a failed waste package and reacts with the waste package components and waste form, and then exits the waste package with no accumulation of reacted water in the waste package. Both of the submodels of the in-package chemistry model are film models in contrast to past in-package chemistry models where all of the waste package pore space was filled with water. The

In-Package Chemistry Abstraction

International Nuclear Information System (INIS)

P.S. Domski

2003-01-01

The work associated with the development of this model report was performed in accordance with the requirements established in ''Technical Work Plan for Waste Form Degradation Modeling, Testing, and Analyses in Support of SR and LA'' (BSC 2002a). The in-package chemistry model and in-package chemistry model abstraction are developed to predict the bulk chemistry inside of a failed waste package and to provide simplified expressions of that chemistry. The purpose of this work is to provide the abstraction model to the Performance Assessment Project and the Waste Form Department for development of geochemical models of the waste package interior. The scope of this model report is to describe the development and validation of the in-package chemistry model and in-package chemistry model abstraction. The in-package chemistry model will consider chemical interactions of water with the waste package materials and the waste form for commercial spent nuclear fuel (CSNF) and codisposed high-level waste glass (HLWG) and N Reactor spent fuel (CDNR). The in-package chemistry model includes two sub-models, the first a water vapor condensation (WVC) model, where water enters a waste package as vapor and forms a film on the waste package components with subsequent film reactions with the waste package materials and waste form--this is a no-flow model, the reacted fluids do not exit the waste package via advection. The second sub-model of the in-package chemistry model is the seepage dripping model (SDM), where water, water that may have seeped into the repository from the surrounding rock, enters a failed waste package and reacts with the waste package components and waste form, and then exits the waste package with no accumulation of reacted water in the waste package. Both of the submodels of the in-package chemistry model are film models in contrast to past in-package chemistry models where all of the waste package pore space was filled with water. The current in

Formation waters of the Norwegian Continental Shelf

Energy Technology Data Exchange (ETDEWEB)

McCartney, R. A.; Rein, E.

2006-03-15

New and previously published analyses of formation waters for the Norwegian Continental Shelf (NCS) have been evaluated and interpreted to determine the compositional distribution of formation waters in the region and factors controlling their compositions, and also to obtain information on subsurface fluid flow. Formation waters in the region are Na-Cl and Na-Ca-Cl-type waters that display a wide range of salinity (2500-212000 mg/kg Cl). Generally, the concentrations of most dissolved constituents are positively correlated with Cl so that their distribution in formation waters largely reflects the variations shown by salinity. Exceptions are SO4 which is generally low (less than 40 mg/l) regardless of Cl, and HCO3 and in-situ pH which are negatively correlated with Cl. The main factors determining the compositions of the formation waters are mixing of meteoric water (probably late-Jurassic to Eocene), ancient seawater and primary brine together with diagenetic reactions that have affected each of these components individually as well as mixtures of them. Evaluation of the distribution of salinity has helped us identify where vertical and/or lateral migration of brine from the evaporites has occurred. This has in turn provided us with information on the presence of leak-points and vertical mixing, although further investigation of the location of evaporites and basin palaeohydrogeology are required to determine whether regional lateral advection has occurred in the past. The results of this study may benefit oil exploration and production activities in the NCS including constraint of hydrocarbon migration models, economic evaluation of undrilled prospects, scale management and compartmentalisation studies. (Author)

Water Chemistry and Clad Corrosion/Deposition Including Fuel Failures. Proceedings of a Technical Meeting

International Nuclear Information System (INIS)

2013-03-01

Corrosion is a principal life limiting degradation mechanism in nuclear steam supply systems, particularly taking into account the trends in increasing fuel burnup, thermal ratings and cycle length. Further, many plants have been operating with varying water chemistry regimes for many years, and issues of crud (deposition of corrosion products on other surfaces in the primary coolant circuit) are of significant concern for operators. At the meeting of the Technical Working Group on Fuel Performance and Technology (TWGFPT) in 2007, it was recommended that a technical meeting be held on the subject of water chemistry and clad corrosion and deposition, including the potential consequences for fuel failures. This proposal was supported by both the Technical Working Group on Advanced Technologies for Light Water Reactors (TWG-LWR) and the Technical Working Group on Advanced Technologies for Heavy Water Reactors (TWG-HWR), with a recommendation to hold the meeting at the National Nuclear Energy Generating Company ENERGOATOM, Ukraine. This technical meeting was part of the IAEA activities on water chemistry, which have included a series of coordinated research projects, the most recent of which, Optimisation of Water Chemistry to Ensure Reliable Water Reactor Fuel Performance at High Burnup and in Ageing Plant (FUWAC) (IAEATECDOC-1666), concluded in 2010. Previous technical meetings were held in Cadarache, France (1985), Portland, Oregon, USA (1989), Rez, Czech Republic (1993), and Hluboka nad Vltavou, Czech Republic (1998). This meeting focused on issues associated with the corrosion of fuel cladding and the deposition of corrosion products from the primary circuit onto the fuel assembly, which can cause overheating and cladding failure or lead to unplanned power shifts due to boron deposition in the clad deposits. Crud deposition on other surfaces increases radiation fields and operator dose and the meeting considered ways to minimize the generation of crud to avoid

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

International Nuclear Information System (INIS)

Ha Hung; Taxen, Claes; Williams, Keith; Scully, John

2011-01-01

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 3 - , SO 4 2- and Cl - -containing waters. → The effective polarization and Ohmic resistance of pits were lower in SO4 2- -containing solutions and greater in Cl - -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 3 - , SO 4 2- and Cl - 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 - 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 in good agreement with artificial pit experiments

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

International Nuclear Information System (INIS)

Zelazny, Miroslaw; Astel, Aleksander; Wolanin, Anna; Malek, Stanislaw

2011-01-01

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.

Steam water cycle chemistry of liquid metal cooled innovative nuclear power reactors

International Nuclear Information System (INIS)

Yurmanov, Victor; Lemekhov, Vadim; Smykov, Vladimir

2012-09-01

selection of chemistry controls is vital for NPPs with liquid metal cooled reactors. This paper highlights principles and approaches to chemistry controls in steam/water cycles of future NPPs with innovative liquid metal cooled reactors. The recommendations on how to arrange chemistry controls in steam/water cycles of future NPPs with innovative liquid metal cooled reactors are based taking into account: - the experience with operation of fossil power industry; - secondary side water chemistry of lead-bismuth eutectics cooled nuclear reactors at submarines; - steam/water cycles of NPPs with sodium cooled fast breeders BN-350 and BN-600; - secondary water chemistry at conventional NPPs with WER, RBMK and some other reactors. (authors)

Student Perceptions of Online Homework Use for Formative Assessment of Learning in Organic Chemistry.

Science.gov (United States)

Richards-Babb, Michelle; Curtis, Reagan; Georgieva, Zomitsa; Penn, John H

2015-11-10

Use of online homework as a formative assessment tool for organic chemistry coursework was examined. Student perceptions of online homework in terms of (i) its ranking relative to other course aspects, (ii) their learning of organic chemistry, and (iii) whether it improved their study habits and how students used it as a learning tool were investigated. Our students perceived the online homework as one of the more useful course aspects for learning organic chemistry content. We found a moderate and statistically significant correlation between online homework performance and final grade. Gender as a variable was ruled out since significant gender differences in overall attitude toward online homework use and course success rates were not found. Our students expressed relatively positive attitudes toward use of online homework with a majority indicating improved study habits (e.g., study in a more consistent manner). Our students used a variety of resources to remediate incorrect responses (e.g., class materials, general online materials, and help from others). However, 39% of our students admitted to guessing at times, instead of working to remediate incorrect responses. In large enrollment organic chemistry courses, online homework may act to bridge the student-instructor gap by providing students with a supportive mechanism for regulated learning of content.

Data processing technologies and diagnostics for water chemistry and corrosion control in nuclear power plants (DAWAC). Report of a coordinated research project 2001-2005

International Nuclear Information System (INIS)

2006-06-01

This publication provides information on the current status and development trends in monitoring, diagnostics and control of water chemistry and corrosion of core and primary circuit materials in water cooled power reactors. It summarizes the results of an IAEA Coordinated Research Project and focuses on the methods for development, qualification and implementation of water chemistry expert systems at nuclear power plants. These systems are needed to have full benefit from using on-line sensors in real time mode when sensor signals, and other chemistry and operational data, are collected and continuously analysed with data acquisition and evaluation software. Technical knowledge was acquired in water chemistry control techniques (grab sampling, on-line monitoring, data collecting and processing, etc), plant chemistry and corrosion diagnostics, plant monitoring (corrosion, chemistry, activity) and plant chemistry improvement (analytical models and practices). This publication covers contributions from leading experts in water chemistry/corrosion, representing organizations from 16 countries with the largest nuclear capacities

WATER CHEMISTRY IN DIFFERENTLY FERTILIZED CARP POUNDS

Directory of Open Access Journals (Sweden)

Krešimir Fašaić

1997-07-01

Full Text Available Water chemistry in carp ponds - fry carp ponds, each of them 2.5 acres big and 1.5 meter deep, as well as in inflow water in the ponds was researched. Fourty days old carp fingerlings were bread in the ponds; stock density of the three day old larvae was 1,000.000 ind˙ha-1. The fingerlings were fed with trouvit and flour. In the ponds and the inflow water the following chemical parameters were examined: : 02, C02, CaC03-, RC03-, outgoing of KMn04, N02-, N03-, NR4+, urea, PO43-, P205 and pH. During the breeding season substantial deviations of all the chemical parameters were stated, but within values that satisfy the needs of the carp ponds. The applied quantity of the mineral fertilizer did not cause a very explicit eutrophication of water in the treated ponds. Certain differences in the quantity of the respective chemical indicators in the fertilized pond variants compared to the nonfertilized variant were insignificant (P**0.05, except the pH value, which increased significantly in the fertilized variants (P<0.05. Compared with the inflow water, in all experimental ponds the quantity of the mineral nitrogen and phosphorus fractions (P<0.05, (P<0.05 has increased. (Tables 5 and 6

Steel corrosion products solubility under conditions simulating various water chemistry parameters in power plants

International Nuclear Information System (INIS)

Slobodov, A.A.; Kritskij, V.G.; Zarembo, V.I.; Puchkov, L.V.

1988-01-01

To simulate construction material corrosion product mass transfer model in power plant circuits calculation of iron oxide and hydroxide solubility, depending on water chemistry parameters: temperature, pH-value, content of dissolved in water hydrogen and oxygen, is carried out

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.

Effects of water chemistry and fluid dynamics on wall thinning behavior. Part 1. Development of FAC model focused on water chemistry and composition of material

International Nuclear Information System (INIS)

Fujiwara, Kazutoshi; Domae, Masafumi; Ohta, Joji; Yoneda, Kimitoshi; Inada, Fumio

2009-01-01

Flow Accelerated Corrosion (FAC), which is one of the important subjects at fossil and nuclear power plans, is caused by the accelerated dissolution of protective oxide film due to the turbulent flow. The influence factors on FAC such as water chemistry, material, and fluid dynamics are closely related to the oxide property so that the risk of FAC can be reduced by the suitable control of water chemistry. There are some FAC models and evaluation codes of FAC rate. Some of them are used in wall thinning management of nuclear power plant in some country. Nevertheless, these FAC codes include many empirical parameters so that some uncertainty to evaluate the synergistic effectiveness of factors are the controversial point for the application of FAC code to wall thinning management in Japanese nuclear power plant. In this study, a FAC model that can evaluate the effect of temperature, NH3 concentration, chromium content, and dissolved oxygen concentration on FAC rate was developed by considering the diffusion of dissolved species. The critical dissolved oxygen concentration, which can inhibit FAC, was also calculated by this model. (author)

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.

Using formative feedback to identify and support first-year chemistry students with missing or misconceptions. A Practice Report

Directory of Open Access Journals (Sweden)

Gwen Lawrie

2013-08-01

Full Text Available Students entering tertiary studies possess a diverse range of prior experiences in their academic preparation for tertiary chemistry so academics need tools to enable them to respond to issues in diversity in conceptual models possessed by entering students. Concept inventories can be used to provide formative feedback to help students identify concepts that they need to address to improve construction of subsequent understanding enabling their learning.Modular, formative learning activities that can be administered inside or outside of class in first year chemistry courses have been developed. These activities address key missing and mis-conceptions possessed by incoming student. Engagement in these learning activities by students and academics will help shift the culture of diagnostic and formative assessment within the tertiary context and address issues around the secondary/tertiary transition. This diagnostic/intervention framework is currently being trialed across five Australian tertiary institutions encompassing a large heterogeneous sample of students.

Formation and fates of nitrosamines and their formation potentials from a surface water source to drinking water treatment plants in Southern Taiwan.

Science.gov (United States)

Chen, Wei-Hsiang; Wang, Chung-Ya; Huang, Tsung-Hsien

2016-10-01

Nitrosamines are toxic and emerging disinfection byproducts. In this study, three drinking water treatment plants (DWTPs) in southern Taiwan treating the same source water in Gaoping River with comparable technologies were selected. The objective was to evaluate the formation and fates of six nitrosamines and their formation potentials (FPs) from a surface water source to drinking water. Albeit decreased further downstream in the river, four nitrosamine-FPs were observed in the source water due to anthropogenic pollution in the upstream areas. In the DWTPs, nitrosamines were formed and NDMA was the main species. While high organic carbon concentrations indicated elevated nitrosamine-FPs in the source water, NDMA formation in the DWTPs was more positively associated with reductions of water parameters that quantify organic matters with double bonded ring structures. Although precursor removal via pre-oxidation is a viable approach to limit nitrosamine formation during post-disinfection, this study clearly indicates that a great portion of NDMA in treated water has been formed in the 1st oxidation step of drinking water treatment. The pre-oxidation simulations in the lab demonstrated the impact of pre-chlorination on nitrosamine formation. Given the limited removal in conventional treatment processes, avoiding nitrosamine-FPs in sources and/or nitrosamine formation during pre-oxidation become important issues to control the threats of nitrosamines in drinking water. Under current circumstance in which pre-oxidation is widely used to optimize the treatment effectiveness in many DWTPs, its adverse effect by forming nitrosamines needs to be carefully minimized and using technologies other than pre-chlorination (e.g., pre-ozonation) may be considered. Copyright © 2016 Elsevier Ltd. All rights reserved.

Some aspects of correction additions optimisation of water chemistry regime of Kozloduy NPP power units 3 and 4

International Nuclear Information System (INIS)

Topalova, I.

2005-01-01

Optimization of the water-chemistry regime is a major corrective measure for minimization of the corrosion processes of the nuclear power unit equipment. Research done in NPP Kozloduy III - IV power units concerning the migration of the corrosion products in the water of secondary circuit as well as the connection between corrosion processes and fluctuation in parameters of the applied water-chemistry regime are reported. Analysis of the dependences obtained lead to conclusions for optimization of the water chemistry regime of secondary circuit and minimization of the corrosion processes and improvement of corrosion condition of metal surfaces. The research is done for the circuit of each of the 8 turbines of the two power units for a period of 10 days. Data received is quantitatively representative /40-50 points/ for performing of analysis and reaching certain conclusions for the water chemistry regime and development of corrosion processes. Dependence of iron and copper concentration in the work medium on the pH, ammonia and hydrazine concentration as well as the dependence of pH on ammonia concentration in case of different quantity and composition of corrosion products on the different power units' equipment metal surfaces are shown. (author)

Stream water chemistry in watersheds receiving different atmospheric inputs of H+, NH4+, NO3-, and SO42-1

Science.gov (United States)

Stottlemyer, R.

1997-01-01

Weekly precipitation and stream water samples were collected from small watersheds in Denali National Park, Alaska, the Fraser Experimental Forest, Colorado, Isle Royale National Park, Michigan, and the Calumet watershed on the south shore of Lake Superior, Michigan. The objective was to determine if stream water chemistry at the mouth and upstream stations reflected precipitation chemistry across a range of atmospheric inputs of H+, NH4+, NO3-, and SO42-. Volume-weighted precipitation H+, NH4+, NO3-, and SO42- concentrations varied 4 to 8 fold with concentrations highest at Calumet and lowest in Denali. Stream water chemistry varied among sites, but did not reflect precipitation chemistry. The Denali watershed, Rock Creek, had the lowest precipitation NO3- and SO42- concentrations, but the highest stream water NO3and SO42- concentrations. Among sites, the ratio of mean monthly upstream NO3- concentration to precipitation NO3- concentration declined (p 90 percent inputs) across inputs ranging from 0.12 to > 6 kg N ha-1 y-1. Factors possibly accounting for the weak or non-existent signal between stream water and precipitation ion concentrations include rapid modification of meltwater and precipitation chemistry by soil processes, and the presence of unfrozen soils which permits winter mineralization and nitrification to occur.

Aquatic Chemistry

International Nuclear Information System (INIS)

Kim, Dong Yeun; Kim, Oh Sik; Kim, Chang Guk; Park, Cheong Gil; Lee, Gwi Hyeon; Lee, Cheol Hui

1987-07-01

This book deals aquatic chemistry, which treats water and environment, chemical kinetics, chemical balance like dynamical characteristic, and thermodynamics, acid-base chemistry such as summary, definition, kinetics, and PH design for mixture of acid-base chemistry, complex chemistry with definition, and kinetics, precipitation and dissolution on summary, kinetics of precipitation and dissolution, and balance design oxidation and resolution with summary, balance of oxidation and resolution.

Water formation via HCl oxidation on Cu(1 0 0)

Energy Technology Data Exchange (ETDEWEB)

Suleiman, Ibrahim A., E-mail: isuleman@taibahu.edu.sa [College of Engineering, Taibah University, Yanbu 41911 (Saudi Arabia); Radny, Marian W. [School of Mathematical and Physical Sciences, The University of Newcastle, Callaghan, NSW 2308 (Australia); Institute of Physics, Poznan University of Technology, 62-956 Poznan (Poland); Gladys, Michael J.; Smith, Phillip V. [School of Mathematical and Physical Sciences, The University of Newcastle, Callaghan, NSW 2308 (Australia); Mackie, John C. [School of Engineering, The University of Newcastle, Callaghan, NSW 2308 (Australia); School of Chemistry, The University of Sydney (Australia); Stockenhuber, Michael; Kennedy, Eric M. [School of Engineering, The University of Newcastle, Callaghan, NSW 2308 (Australia); Dlugogorski, Bogdan Z. [School of Engineering, The University of Newcastle, Callaghan, NSW 2308 (Australia); School of Engineering and Information Technology, Murdoch University, Perth (Australia)

2014-04-01

Graphical abstract: This work investigates water formation on the Cu(1 0 0) surface via HCl oxidation using density functional theory and periodic slabs. We show that there are two different pathways for water formation on the surface depending on the temperature and oxygen coverage. - Highlights: • Pre-adsorbed chlorine increases the stability of water on Cu(1 0 0). • Two different pathways describe water formation on Cu(1 0 0) via HCl oxidation. • The mechanism of H{sub 2}O formation depends on the temperature and oxygen coverage. - Abstract: Using density functional theory and periodic slabs, we have studied water formation via HCl oxidation on the Cu(1 0 0) surface. We show that while adsorbed chlorine increases the stability of water on the Cu(1 0 0) surface, water molecules dissociate immediately when located next to an oxygen atom. We also show that these competing interactions, when arising from HCl reacting with oxygen on Cu(1 0 0), lead to water formation according to two different pathways depending on the temperature and oxygen coverage.

Assessment of rain water chemistry in the Lucknow metropolitan city

Science.gov (United States)

Sharma, Purnima; Rai, Vibhuti

2018-05-01

Lucknow metropolitan city is one of the most populated cities of India, which have been facing many problems such as chaotic urbanization, overpopulation, water scarcity, waterlogging, etc., among these water scarcity is one of the important problem. Rain water harvesting is a futuristic tool for mitigation of water scarcity problem through conservation and storage of rain water. This rain water can be used for all purposes by human beings, thus it is necessary to check the chemistry of rain water. The rain water samples were collected from the five zones of Lucknow city. For the comparative study, water samples have been collected from two different dates first from first rainfall and second after 3 days of interval in the second rainfall. The heavy metal concentrations were found in both first and second rainfall water samples in all zones of Lucknow city. The concentration of chromium, cadmium and lead were found to be sufficiently high in several samples. These heavy metals show the concentration above the permissible limit as set by WHO, which can cause various adverse health impacts.

Primary water chemistry improvement for radiation exposure reduction at Japanese PWR Plants

Energy Technology Data Exchange (ETDEWEB)

Nishizawa, Eiichi [Omiya Technical Institute, Saitama-ken (Japan)

1995-03-01

Radiation exposure during the refueling outages at Japanese Pressurized Water Reactor (PWR) Plants has been gradually decreased through continuous efforts keeping the radiation dose rates at relatively low level. The improvement of primary water chemistry in respect to reduction of the radiation sources appears as one of the most important contributions to the achieved results and can be classified by the plant operation conditions as follows

From trace chemistry to single atom chemistry

International Nuclear Information System (INIS)

Adloff, J.P.

1993-01-01

Hot atom chemistry in the vast majority of experimental works deals with the trace amount of radioactive matters. Accordingly, the concept of trace chemistry is at the heart of hot atom chemistry. Some aspects of the chemistry at trace scale and at subtrace scale are presented together with the related problems of speciation and the complication which may arise due to the formation of radio colloids. The examples of 127 I(n,γ) 128 I and 132 Te (β - ) 132 I are shown, and the method based on radioactivity was used. The procedure of separating the elements in pitchblende is shown as the example of the chemistry of traces. 13 27 Al+ 2 4 He→ 0 1 n+ 15 30 P and 15 30 P→ 14 30 Si+e + +V are shown, and how to recognize the presence of radioactive colloids is explained. The formation of radiocolloids is by the sorption of a trace radioelement on pre-existing colloidal impurity or the self-condensation of monomeric species. The temporal parameters of the nature of reactions at trace concentration are listed. The examples of Class A and Class B reactions are shown. The kinetics of reactions at trace level, radon concentration, anthropogenic Pu and natural Pu in environment, the behavior of Pu atoms and so on are described. (K.I.)

PWR secondary water chemistry study

International Nuclear Information System (INIS)

Pearl, W.L.; Sawochka, S.G.; Copley, S.E.; Siegwarth, D.P.

1981-01-01

Secondary water chemistry studies have been performed at ten operating PWRs for the past several years. The program includes seven PWRs with recirculating U-tube steam generators, and three once-through steam generator (OTSG) PWRs. Program results indicate that during periods of minimal condenser inleakage, condensate polishers do not remove significant quantities of sodium, chloride and sulfate. At higher inlet impurity levels, demineralizer removal efficiencies improve markedly. Corrosion product removal efficiencies generally are 60 to 95% depending on system design and operating practices. Significant quantities of sodium and chloride 'hide out' in steam generators with a portion returning during transients, particularly during plant shutdowns. In OTSG PWRs, a significant portion of the total sodium and chloride transported via the steam is removed with the moisture separator drains (MSD) and returned to the OTSG when MSDs are pumped forward. Partial return of MSDs to the condenser would result in reduced feedwater and steam impurity levels. (author)

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.

A coordination chemistry approach for modeling trace element adsorption

International Nuclear Information System (INIS)

Bourg, A.C.M.

1986-01-01

The traditional distribution coefficient, Kd, is highly dependent on the water chemistry and the surface properties of the geological system being studied and is therefore quite inappropriate for use in predictive models. Adsorption, one of the many processes included in Kd values, is described here using a coordination chemistry approach. The concept of adsorption of cationic trace elements by solid hydrous oxides can be applied to natural solids. The adsorption process is thus understood in terms of a classical complexation leading to the formation of surface (heterogeneous) ligands. Applications of this concept to some freshwater, estuarine and marine environments are discussed. (author)

Formation rate of water masses in the Japan Sea

International Nuclear Information System (INIS)

Kawamura, Hideyuki; Ito, Toshimichi; Yoon, Jong-Hwan

2007-01-01

Water masses in the subsurface and the intermediate layer are actively formed due to strong winter convection in the Japan Sea. It is probable that some fraction of pollution is carried into the layer below the sea surface together with these water masses, so it is important to estimate the formation rate and turnover time of water masses to study the fate of pollutants. The present study estimates the annual formation rate and the turnover time of water masses using a three-dimensional ocean circulation model and a particle chasing method. The total annual formation rate of water masses below the sea surface amounted to about 3.53±0.55 Sv in the Japan Sea. Regarding representative intermediate water masses, the annual formation rate of the Upper portion of the Japan Sea Proper Water (UJSPW) and the Japan Sea Intermediate Water (JSIW) were estimated to be about 0.38±0.11 and 1.43±0.16 Sv, respectively, although there was little evidence of the formation of deeper water masses below a depth of about 1500 m in a numerical experiment. An estimate of turnover time shows that the UJSPW and the JSIW circulate in the intermediate layer of the Japan Sea with timescales of about 22.1 and 2.2 years, respectively. (author)

NATO Advanced Study Institute on Pollutants from Combustion Formation and Impact on Atmospheric Chemistry

CERN Document Server

2000-01-01

This volume is based on the lectures presented at the NATO Advanced Study Institute: (ASI) «Pollutants Formation from Combustion. Formation Mechanisms and Impact on th th Atmospheric Chemistry» held in Maratea, Italy, from 13 to 26 september 1998. Preservation of the environment is of increasing concern in individual countries but also at continental or world scales. The structure of a NATO ASI which involve lecturers and participants of different nationalities was thought as especially well suited to address environmental issues. As combustion is known to substantially contribute to the damaging of the atmosphere, it was natural to concentrate the ASI program on reviewing the currently available knowledge of the formation mechanisms of the main pollutants liberated by combustion systems. In most situations, pollutants are present as trace components and their formation and removal is strongly conditioned by the chemical reactions initiated by fuel consumption. Therefore specific lectures were aimed at defi...

Using computer simulations to improve concept formation in chemistry

African Journals Online (AJOL)

The goal of this research project was to investigate whether computer simulations used as a visually-supporting teaching strategy, can improve concept formation with regard to molecules and chemical bonding, as found in water. Both the qualitative and quantitative evaluation of responses supported the positive outcome ...

Brine Pockets in the Icy Shell on Europa: Distribution, Chemistry, and Habitability

Science.gov (United States)

Zolotov, M. Yu; Shock, E. L.; Barr, A. C.; Pappalardo, R. T.

2004-01-01

On Earth, sea ice is rich in brine, salt, and gas inclusions that form through capturing of seawater during ice formation. Cooling of the ice over time leads to sequential freezing of captured sea-water, precipitation of salts, exsolution of gases, and formation of brine channels and pockets. Distribution and composition of brines in sea ice depend on the rate of ice formation, vertical temperature gradient, and the age of the ice. With aging, the abundance of brine pockets decreases through downward migration. De- spite low temperatures and elevated salinities, brines in sea ice provide a habitat for photosynthetic and chemosynthetic organisms. On Europa, brine pockets and channels could exist in the icy shell that may be from a few km to a few tens of km thick and is probably underlain by a water ocean. If the icy shell is relatively thick, convection could develop, affecting the temperature pattern in the ice. To predict the distribution and chemistry of brine pockets in the icy shell we have combined numerical models of the temperature distribution within a convecting shell, a model for oceanic chemistry, and a model for freezing of Europan oceanic water. Possible effects of brine and gas inclusions on ice rheology and tectonics are discussed.

Analysis of realization of the water chemistry modes in the NPP with the RBMK-1000 and main directions of their improvement

International Nuclear Information System (INIS)

Kritskij, V.G.; Tyapkov, V.F.; Belous, V.N.; Egorova, T.M.; Gost'kov, V.V.; Tishkov, V.M.; Yatsko, O.V.

2005-01-01

Paper deals with the analysis of normalization of the RBMK reactor NPP water chemistry conditions. One analyzed the imposed restrictions at deviation of the normalized parameters from the ones recommended for the normal operating conditions. Paper contains data on water chemistry management and describes measures to improve radiation situation near NPP reactor equipment. One studied the reasons of corrosion damage of the RBMK-1000 reactor NPP pipelines and the ways to prevent them via optimization and improvement of water chemistry conditions [ru

Study on the influence of water chemistry on fuel cladding behaviour of LWR in Japan

International Nuclear Information System (INIS)

Mishima, Y.

1983-01-01

This article presents the results of the study on the influence of water chemistry on fuel cladding behaviour, which has been performed for more than ten years on BWRs and PWRs in Japan. The post irradiation examination (P.I.E.) program of commercial reactor fuel assembly which was explained at Tokyo meeting in 1981 includes an investigation of the characteristics and build-up conditions of crud deposited on mainly BWR fuel cladding. This article also provides a summary of the results of the investigation and shows how the results are utilized for establishing effective water chemistry measures

Chemistry and mineralogy of some Plio-Pleistocene tuffs from the Shungura Formation, southwest Ethiopia

Science.gov (United States)

Martz, A. M.; Brown, F. H.

1981-09-01

The Shungura Formation of southwestern Ethiopia has yielded many tens of thousands of vertebrate fossils including hominids and microvertebrates, and in addition has also yielded fossil wood, pollen, and invertebrates. Widespread tuffs have made subdivision and detailed mapping of the formation possible, have provided material for potassium-argon dating, and have allowed direct lithostratigraphic correlation with the Koobi Fora Formation in northern Kenya. The basis for correlation between the two formations is the distinctive chemistry of the tuffs, but systematic chemical variation within some tuffs invalidates some statistical correlation techniques. Here chemical analysis of glass separates and minerals from tuffs of the Shungura and Usno Formations are presented which may allow further ties to be established when data become available on other tuffs of the Koobi Fora Formation. The tuffs consist primarily of glass, but also contain phenocrysts of anorthoclase, hedenbergitic pyroxene, sodic amphibole, ilmenite, titanomagnetite, chevkinite, quartz, zircon, and rarely orthopyroxene and plagioclase. The glasses show evidence of alkali loss during hydration, and are not now peralkaline, although it is likely that they were initially. The source volcanoes were most likely situated within the Ethiopian rift valley, or on its margins.

Overview of VVER water chemistry

International Nuclear Information System (INIS)

Ganesh, S.; Selvaraj, S.; Balasubramanian, M.R.; Selvavinayagam, P.; Sundar, R.S.

2007-01-01

Kudankulam Nuclear Power project is having twin units of 1000MWe of VVER type. This paper highlights the different analytical techniques that are followed to maintain the system chemistry within the technical specifications. This paper also briefs the different chemicals that are added to the systems and how they are monitored. Basic differences with respect to chemistry between a PHWR and VVER are also highlighted in this paper. (author)

5. International seminar on primary and secondary side water chemistry of nuclear power plants

International Nuclear Information System (INIS)

2001-01-01

The major subjects of the meetings are: water chemistry of primary and secondary coolant circuits of PWR type reactors (mainly WWER types), corrosion of steam generators, decontamination processes, treatment of radioactive waste waters and related subjects. All the 29 papers were individually indexed and abstracted for the INIS database. (R.P.)

5. International seminar on primary and secondary side water chemistry of nuclear power plants

Energy Technology Data Exchange (ETDEWEB)

NONE

2001-07-01

The major subjects of the meetings are: water chemistry of primary and secondary coolant circuits of PWR type reactors (mainly WWER types), corrosion of steam generators, decontamination processes, treatment of radioactive waste waters and related subjects. All the 29 papers were individually indexed and abstracted for the INIS database. (R.P.)

Influence of intermittent water releases on groundwater chemistry at the lower reaches of the Tarim River, China.

Science.gov (United States)

Chen, Yong-jin; Chen, Ya-ning; Liu, Jia-zhen; Zhang, Er-xun

2009-11-01

Based on the data of the depths and the chemical properties of groundwater, salinity in the soil profile, and the basic information on each delivery of water collected from the years 2000 to 2006, the varied character of groundwater chemistry and related factors were studied. The results confirmed the three stages of the variations in groundwater chemistry influenced by the intermittent water deliveries. The factors that had close relations to the variations in groundwater chemistry were the distances of monitoring wells from the water channel, the depths of the groundwater, water flux in watercourse, and the salinities in soils. The relations between chemical variation and groundwater depths indicated that the water quality was the best with the groundwater varying from 5 to 6 m. In addition, the constructive species in the study area can survive well with the depth of groundwater varying from 5 to 6 m, so the rational depth of groundwater in the lower reaches of the Tarim River should be 5 m or so. The redistribution of salts in the soil profile and its relations to the chemical properties and depths of groundwater revealed the linear water delivery at present combining with surface water supply in proper sections would promote water quality optimized and speed up the pace of ecological restoration in the study area.

Investigation of primary cooling water chemistry following the partial meltdown of Pu-Be neutron source in Tehran Research Reactor Core (TRR)

Energy Technology Data Exchange (ETDEWEB)

Aghoyeh, Reza Gholizadeh [School of Research and Development of Nuclear Reactors and Accelerators, Nuclear Science and Technology Research Institute (NSTRI), Atomic Energy Organization of Iran (AEOI), P.O. Box: 14155-1339, Tehran (Iran, Islamic Republic of); Khalafi, Hossein, E-mail: hkhalafi@aeoi.org.i [School of Research and Development of Nuclear Reactors and Accelerators, Nuclear Science and Technology Research Institute (NSTRI), Atomic Energy Organization of Iran (AEOI), P.O. Box: 14155-1339, Tehran (Iran, Islamic Republic of)

2011-03-15

Research highlights: Effect of Pu-Be neutron source meltdown in core on reactor water chemistry. Water chemistry of primary cooling before, during and after of above incident was compared. Training importance. Management of nuclear incident and accident. - Abstract: Effect of Pu-Be neutron source meltdown in core on reactor water chemistry was main aim of this study. Leaving the neutron source in the core after reactor power exceeds a few hundred Watts was the main reason for its partial meltdown. Water chemistry of primary cooling before, during and after of above incident was compared. Activity of some radio-nuclides such as Ba-140, La-140, I-131, I-132, Te-132 and Xe-135 increased. Other radio-nuclides such as Nd-147, Xe-133, Sr-91, I-133 and I-135 are also detected which were not existed before this incident.

Chemistry of water and steam in power plants and related technologies. Glossary of terms and definitions English - German; German - English

Energy Technology Data Exchange (ETDEWEB)

Schmitz, H.P.; Teutenberg, U.

2006-07-01

This new edition of a technical dictionary is an evaluation of the technical terms found in the domestic and foreign literature and in information brochures of specialist firms, directives, guidelines, standards, etc. This dictionary contains more than 3,000 terms mainly with definitions with respect to the chemistry of water and steam in power plants along with the related types of water (untreated water, feedwater and boiler water, make-up water, waste water) and the water treatment processes (ion exchange, membrane process, etc.), water conditioning and chemical analysis, internal cleaning of steam generating plants (e.g. flushing, boiling-out, pre-operational and operational acid cleaning, steam blowing) as well as fundamentals of water chemistry. The technical knowledge of the authors, Heinz-Peter Schmitz, FDBR, with more than 25 years professional experience as translator/official in charge of documentation and Ulrich Teutenberg, Babcock/Hitachi with more than 30 years professional experience as senior consultant for water chemistry and commissioning is reflected in this dictionary. Part 1 contains the English-German version, Part 2 the German-English version. (orig.)

A novel bedside diagnostic test for methanol poisoning using dry chemistry for formate.

Science.gov (United States)

Hovda, Knut Erik; Gadeholt, Gaut; Evtodienko, Vladimir; Jacobsen, Dag

2015-11-01

The standard diagnostic approach to methanol poisoning is chromatographic measurement of methanol on centrally placed stationary equipment. Methanol poisoning in places where such equipment is unavailable is thus often not diagnosed. Methanol is metabolized to a toxic metabolite, formate; the presence of this compound indicates methanol poisoning. We have developed an enzymatic test for formate and modified it into a portable dry chemistry system that could be used anywhere. The method consists of two enzymatic steps: Formation of NADH from NAD by formate dehydrogenase, and subsequent use of NADH as a reductant of a tetrazolium into a formazan dye that can be quantified photometrically or visually. The photometer gave a good correlation of R(2) = 0.9893 in serum and R(2) = 0.9949 in whole blood, showing an instrumental detection limit of less than 1 mM (4.5 mg/dL). The visual readings showed a correlation of R(2) = 0.8966. Users experienced some difficulty in separating the negative control from the low positives. We have documented the feasibility of an affordable formate strip test for bedside diagnosis of methanol poisoning and for screening of metabolic acidosis of unknown origin. Visual reading is possible, but a reader will improve reliability at lower levels of formate. Future studies are necessary to study the sensitivity and specificity towards other causes of metabolic acidosis and other acids present in human blood.

On the Formation of Interstellar Water Ice: Constraints from a Search for Hydrogen Peroxide Ice in Molecular Clouds

Science.gov (United States)

Smith, R. G.; Charnely, S. B.; Pendleton, Y. J.; Wright, C. M.; Maldoni, M. M.; Robinson, G.

2011-01-01

Recent surface chemistry experiments have shown that the hydrogenation of molecular oxygen on interstellar dust grains is a plausible formation mechanism, via hydrogen peroxide (H2O2), for the production of water (H2O) ice mantles in the dense interstellar medium. Theoretical chemistry models also predict the formation of a significant abundance of H2O2 ice in grain mantles by this route. At their upper limits, the predicted and experimental abundances are sufficiently high that H2O2 should be detectable in molecular cloud ice spectra. To investigate this further, laboratory spectra have been obtained for H2O2/H2O ice films between 2.5 and 200 micron, from 10 to 180 K, containing 3%, 30%, and 97% H2O2 ice. Integrated absorbances for all the absorption features in low-temperature H2O2 ice have been derived from these spectra. For identifying H2O2 ice, the key results are the presence of unique features near 3.5, 7.0, and 11.3 micron. Comparing the laboratory spectra with the spectra of a group of 24 protostars and field stars, all of which have strong H2O ice absorption bands, no absorption features are found that can definitely be identified with H2O2 ice. In the absence of definite H2O2 features, the H2O2 abundance is constrained by its possible contribution to the weak absorption feature near 3.47 micron found on the long-wavelength wing of the 3 micron H2O ice band. This gives an average upper limit for H2O2, as a percentage of H2O, of 9% +/- 4%. This is a strong constraint on parameters for surface chemistry experiments and dense cloud chemistry models.

PWR primary system chemistry control during hot functional testing

International Nuclear Information System (INIS)

Reid, Richard D.; Little, Michael J.

2014-01-01

Hot Functional Testing (HFT) involves a number of pre-operational exercises performed to confirm the operability of plant systems at conditions expected during both normal and off-normal operation of a pressurized water reactor (PWR), including operability of safety systems. While the primary purposes of HFT are to demonstrate operability of plant systems and satisfy regulatory requirements, chemistry control during HFT is important to long-term integrity and performance of plant systems. Specifically, HFT is the first time plant equipment is exposed to high temperature water and the chemistry maintained during HFT can impact the passivation layers that form on wetted surfaces and long-term release of metals from these surfaces. Metals released from the inner surfaces of steam generator tubing and reactor coolant loop piping become activated in the core and can redeposit on ex-core surfaces. Because HFT is performed before fuel is loaded in the core, HFT provides an opportunity to produce a passive layer on primary surfaces that is free of activated corrosion products, resistant to metals release during subsequent plant operation, and also resistant to incorporation of activated corrosion products (once fuel is loaded in the core). Thus, maintaining desirable primary chemistry control during HFT is important for source term management, minimization of future shutdown activity releases, minimization of dose rates, and asset preservation. This paper presents an overview of passive film formation in the austenitic stainless steel and high nickel alloys that make up the majority of the primary circuit in advanced PWR designs. Based on this information, a summary is provided of the effects on passive film formation of key chemistry parameters that may be controlled during HFT. (author)

Primary circuit water chemistry during shutdown period at Kalinin NPP

International Nuclear Information System (INIS)

Gorbatenko, S.; Otchenashev, G.; Yurmanov, V.

2005-01-01

The primary circuit water chemistry feature at Kalinin NPP is using of special up-dated regime during the period of unit shutdown for refueling. The main objective of up-dated regime is removing from the circuit long time living corrosion products on SVO-2 ion exchange filters with the purpose of dose rates reduction from the equipment and in such a way reduction of maintenance personnel overexposure. (N.T.)

Mercury Redox Chemistry in Waters of the Eastern Asian Seas: From Polluted Coast to Clean Open Ocean.

Science.gov (United States)

Ci, Zhijia; Zhang, Xiaoshan; Yin, Yongguang; Chen, Jinsheng; Wang, Shiwei

2016-03-01

We performed incubation experiments using seawaters from representative marine environments of the eastern Asian seas to determine the mercury (Hg) available for photoreduction (Hgr(II)), to investigate the Hg redox reaction kinetics, and to explore the effect of environmental factors and water chemistry on the Hg redox chemistry. Results show that Hgr(II) accounted for a considerable fraction of total Hg (THg) (%Hgr(II)/THg: 24.90 ± 10.55%, n = 27) and positively correlated with THg. Filtration decreased the Hgr(II) pool of waters with high suspended particulate matter (SPM). The positive linear relationships were found between pseudo-first order rate constants of gross Hg(II) photoreduction (kr) and gross Hg(0) photo-oxidation (ko) with photosynthetically active radiation (PAR). Under the condition of PAR of 1 m mol m(-2) s(-1), the kr were significantly (p < 0.05) lower than ko (kr/ko: 0.86 ± 0.22). The Hg(0) dark oxidation were significantly higher than the Hg(II) dark reduction. The Hg(II) dark reduction was positively correlated to THg, and the anaerobic condition favored the Hg(II) dark reduction. Filtration significantly influenced the Hg photoredox chemistry of waters with high SPM. UVB radiation was important for both Hg(II) photoreduction and Hg(0) photo-oxidation, and the role of other wavebands in photoinduced transformations of Hg varied with the water chemistry.

Parametric tests of the effects of water chemistry impurities on corrosion of Zr-alloys under simulated BWR condition

Energy Technology Data Exchange (ETDEWEB)

Shimada, S; Ito, K [Nippon Nuclear Fuel Development Co. Ltd., Oarai, Ibaraki (Japan); Lin, C C [GE Nucklear Energy (United States); Cheng, B [Electric Power Research Inst. (United States); Ikeda, T [Toshiba Corp. (Japan); Oguma, M [Hitachi, Ltd (Japan); Takei, T [Tokyo Electric Power Co., Inc. (Japan); Vitanza, C; Karlsen, T M [Institutt for Energiteknikk, Halden (Norway). OECD Halden Reaktor Projekt

1997-02-01

The Halden BWR corrosion test loop was constructed to evaluate the impact of water chemistry variables, heat flux and boiling condition on corrosion performance of Zr-alloys in a simulated BWR environment. The loop consists of two in-core rigs, one for testing fuel rod segments and the other for evaluating water chemistry variables utilizing four miniautoclaves. Ten coupon specimens are enclosed in each miniautoclave. The Zr-alloys for the test include Zircaloy-2 having different nodular corrosion resistance and five new alloys. The first and second of the six irradiation tests planned in this program were completed. Post-irradiation examination of those test specimens have shown that the test loop is capable of producing nodular corrosion on the fuel rod cladding tested under the reference chemistry condition. The miniautoclave tests showed that nodular corrosion could be formed without flux and boiling under some water chemistry conditions and the new alloys, generally, had higher corrosion resistance than the Zircaloy in high oxygen environments. (author). 5 refs, 4 figs, 5 tabs.

Impact of chemical oxidation and water acidification on the mineralogical and physico-chemical properties of the Tournemire argillaceous formation

International Nuclear Information System (INIS)

Charpentier, D.

2001-11-01

The French Institute for Protection and Nuclear Safety (IPSN) has selected a site near Tournemire (France) for research programmes on deep geological waste disposal in clay-rich rock formation. A railway tunnel was built about 100 years ago through the thick indurated Toarcian argillite of the Tournemire Massif and two galleries were constructed five years ago. They are used to study the evolution of rock mineralogical composition, texture, water content and water-rock interactions in the excavated disturbed zone. Multi-scale and multi-technique investigations were carried out on the evolution of physical and mineralogical rock properties. Experiments and numerical modelling were used to predict changes due to water-rock interactions and subsequent rock mineralogy and water chemistry modifications. The argillite consists of detrital clay-rich layers and carbonate layers. Pyrites are always present in significant amounts (2 to 2.5 %). The rock presents very low porosity and very low water content (around 3 %). Leaching experiments show that the interstitial water is Na and SO 4 -rich and Cl-poor. The tunnel and galleries digging induces fracture formation. In the altered samples, the clay particles show a better orientation in the stratification plan, which increases the porosity. The oxidation effect yields to mineralogical transformation on the surfaces of the argillite: oxidation of pyrite, dissolution of calcite, dissolution of illite layers in interstratified I/S and formation of gypsum, Fe-oxi/hydroxides, celestite and jarosite. During cycles of hydration/dehydration, condensation water interacts with the argillite and quickly becomes Ca and SO 4 -rich. The local dissolution of clay particles leads to an increase of the chloride and potassium water content. These phenomena are important for the consideration of the underground work stability, especially the evolution of the water-rock equilibria during the re-hydration of the excavated disturbed zones. (author)

NDMA formation kinetics from three pharmaceuticals in four water matrices.

Science.gov (United States)

Shen, Ruqiao; Andrews, Susan A

2011-11-01

N, N-nitrosodimethylamine (NDMA) is an emerging disinfection by-product (DBP) that has been widely detected in many drinking water systems and commonly associated with the chloramine disinfection process. Some amine-based pharmaceuticals have been demonstrated to form NDMA during chloramination, but studies regarding the reaction kinetics are largely lacking. This study investigates the NDMA formation kinetics from ranitidine, chlorphenamine, and doxylamine under practical chloramine disinfection conditions. The formation profile was monitored in both lab-grade water and real water matrices, and a statistical model is proposed to describe and predict the NDMA formation from selected pharmaceuticals in various water matrices. The results indicate the significant impact of water matrix components and reaction time on the NDMA formation from selected pharmaceuticals, and provide fresh insights on the estimation of ultimate NDMA formation potential from pharmaceutical precursors. Copyright © 2011 Elsevier Ltd. All rights reserved.

Impact of water chemistry on surface charge and aggregation of polystyrene microspheres suspensions.

Science.gov (United States)

Lu, Songhua; Zhu, Kairuo; Song, Wencheng; Song, Gang; Chen, Diyun; Hayat, Tasawar; Alharbi, Njud S; Chen, Changlun; Sun, Yubing

2018-07-15

The discharge of microplastics into aquatic environment poses the potential threat to the hydrocoles and human health. The fate and transport of microplastics in aqueous solutions are significantly influenced by water chemistry. In this study, the effect of water chemistry (i.e., pH, foreign salts and humic acid) on the surface charge and aggregation of polystyrene microsphere in aqueous solutions was conducted by batch, zeta potentials, hydrodynamic diameters, FT-IR and XPS analysis. Compared to Na + and K + , the lower negative zeta potentials and larger hydrodynamic diameters of polystyrene microspheres after introduction of Mg 2+ were observed within a wide range of pH (2.0-11.0) and ionic strength (IS, 0.01-500mmol/L). No effect of Cl - , HCO 3 - and SO 4 2- on the zeta potentials and hydrodynamic diameters of polystyrene microspheres was observed at low IS concentrations (10mmol/L). The zeta potentials of polystyrene microspheres after HA addition were decreased at pH2.0-11.0, whereas the lower hydrodynamic diameters were observed at pH<4.0. According to FT-IR and XPS analysis, the change in surface properties of polystyrene microspheres after addition of hydrated Mg 2+ and HA was attributed to surface electrostatic and/or steric repulsions. These investigations are crucial for understanding the effect of water chemistry on colloidal stability of microplastics in aquatic environment. Copyright © 2018 Elsevier B.V. All rights reserved.

Evaluating the effects of variable water chemistry on bacterial transport during infiltration.

Science.gov (United States)

Zhang, Haibo; Nordin, Nahjan Amer; Olson, Mira S

2013-07-01

Bacterial infiltration through the subsurface has been studied experimentally under different conditions of interest and is dependent on a variety of physical, chemical and biological factors. However, most bacterial transport studies fail to adequately represent the complex processes occurring in natural systems. Bacteria are frequently detected in stormwater runoff, and may present risk of microbial contamination during stormwater recharge into groundwater. Mixing of stormwater runoff with groundwater during infiltration results in changes in local solution chemistry, which may lead to changes in both bacterial and collector surface properties and subsequent bacterial attachment rates. This study focuses on quantifying changes in bacterial transport behavior under variable solution chemistry, and on comparing the influences of chemical variability and physical variability on bacterial attachment rates. Bacterial attachment rate at the soil-water interface was predicted analytically using a combined rate equation, which varies temporally and spatially with respect to changes in solution chemistry. Two-phase Monte Carlo analysis was conducted and an overall input-output correlation coefficient was calculated to quantitatively describe the importance of physiochemical variation on the estimates of attachment rate. Among physical variables, soil particle size has the highest correlation coefficient, followed by porosity of the soil media, bacterial size and flow velocity. Among chemical variables, ionic strength has the highest correlation coefficient. A semi-reactive microbial transport model was developed within HP1 (HYDRUS1D-PHREEQC) and applied to column transport experiments with constant and variable solution chemistries. Bacterial attachment rates varied from 9.10×10(-3)min(-1) to 3.71×10(-3)min(-1) due to mixing of synthetic stormwater (SSW) with artificial groundwater (AGW), while bacterial attachment remained constant at 9.10×10(-3)min(-1) in a constant

Current status of water chemistry in Japan

Energy Technology Data Exchange (ETDEWEB)

Ishigure, K. [Saitama Inst. of Tech. (Japan)

2002-07-01

At present 28 BWRs including 2 ABWRs and 23 PWRs are in operation in Japan and generated 36.8{open_square} of total electric power in 1998. Totally 4 BWRs, of which two are ABWRs, are now under construction, and one BWR together with one ABWR is in the stage of planning. One gas-cooled reactor (Tokai-1) was shut down permanently in 1998 and last year entered into decommissioning stage. According to the Japanese 2001 plan of electric power supply, 13 nuclear power plants newly constructed are to start operation in the next 10 years. In this paper the recent status of water chemistry technology in Japanese nuclear power plants is briefly summarized together with a touch upon the activities in the fundamental research. (author)

Current status of water chemistry in Japan

International Nuclear Information System (INIS)

Ishigure, K.

2002-01-01

At present 28 BWRs including 2 ABWRs and 23 PWRs are in operation in Japan and generated 36.8□ of total electric power in 1998. Totally 4 BWRs, of which two are ABWRs, are now under construction, and one BWR together with one ABWR is in the stage of planning. One gas-cooled reactor (Tokai-1) was shut down permanently in 1998 and last year entered into decommissioning stage. According to the Japanese 2001 plan of electric power supply, 13 nuclear power plants newly constructed are to start operation in the next 10 years. In this paper the recent status of water chemistry technology in Japanese nuclear power plants is briefly summarized together with a touch upon the activities in the fundamental research. (author)

The role of water chemistry and geomorphic control in the presence of Didymosphenia geminata in Quebec

Science.gov (United States)

Gillis, C.; Gabor, R. S.; Cullis, J. D.; Ran, L.; Hassan, M. A.

2010-12-01

Didymosphenia geminata (didymo), an invasive diatom, was first officially observed and identified in the Matapedia River in Eastern Quebec in July 2006. This Atlantic salmon fishing river has several characteristics shown to favor didymo's ability to form thick, extensive benthic mats, including stable flow and oligotrophic nutrient conditions. Since the incursion, rapid colonization and inter-catchment transfer processes were observed, notably in surrounding watersheds on the Gaspé Peninsula as well as in northern New-Brunswick. All affected watersheds share favorable characteristics for didymo growth, including high light, low nutrient waters, and stable substrate. The nearby North Shore of the St. Lawrence, which also contains rivers with conditions that would favor didymo growth, has not yet shown didymo presence. This system provides a comparison to identify necessary parameters for didymo growth, with differences primarily due to geology-driven water chemistry. Pre-incursion water chemistry was compared between the two regions. Rivers in the region where didymo is present displayed a high alkalinity and corresponding higher pH, due to increases concentrations of magnesium and calcium, than rivers in regions where didymo has not appeared. Also, rivers with didymo show a lower amount of color-causing compounds, such as organic carbon, and clearer water, which supports the theory that high light levels encourage didymo growth. In addition to water chemistry, channel morphology, bed stability and flow patterns are also believed to be key elements in determining the presence of this benthic diatom. In 2007, channel morphology, bed texture, bankfull depth and width, local bed slope and didymo presence were surveyed on a 65 km stretch of the Matapedia River. Relative frequency of didymo presence showed that didymo blooms are most likely to appear in cobble-riffles than in any other morphologies. In fact, cobble riffles promote didymo establishment due to shallow

Comet Halley and interstellar chemistry

International Nuclear Information System (INIS)

Snyder, L.E.

1989-01-01

How complex is the chemistry of the interstellar medium? How far does it evolve and how has it interacted with the chemistry of the solar system? Are the galactic chemical processes destroyed, preserved, or even enhanced in comets? Are biogenic molecules formed in space and have the formation mechanisms interacted in any way with prebiotic organic chemical processes on the early earth? Radio molecular studies of comets are important for probing deep into the coma and nuclear region and thus may help answer these questions. Comets are believed to be pristine samples of the debris left from the formation of the solar system and may have been the carrier between interstellar and terrestrial prebiotic chemistries. Recent observations of Comet Halley and subsequent comets have given the author an excellent opportunity to study the relationship between interstellar molecular chemistry and cometary chemistry

THE CHEMISTRY OF POPULATION III SUPERNOVA EJECTA. I. FORMATION OF MOLECULES IN THE EARLY UNIVERSE

International Nuclear Information System (INIS)

Cherchneff, Isabelle; Dwek, Eli

2009-01-01

We study the formation and destruction of molecules in the ejecta of Population III supernovae (SNe) using a chemical kinetic approach to follow the evolution of molecular abundances from day 100 to day 1000 after explosion. The chemical species included in the study range from simple diatomic molecules to more complex dust precursor species. All relevant molecule formation and destruction processes that are unique to the SN environment are considered. Our work focuses on zero-metallicity progenitors with masses of 20, 170, and 270 M sun , and we study the effect of different levels of heavy element mixing and the inward diffusion of hydrogen and helium on the ejecta chemistry. We show that the ejecta chemistry does not reach a steady state within the relevant timespan (∼3 yr) for molecule formation, thus invalidating previous results relying on this assumption. The primary species formed in the harsh SN environment are O 2 , CO, SiS, and SO. The SiO, formed as early as 200 days after explosion, is rapidly depleted by the formation of silica molecular precursors in the ejecta. The rapid conversion of CO to C 2 and its thermal fractionation at temperatures above 5000 K allow for the formation of carbon chains in the oxygen-rich zone of the unmixed models, providing an important pathway for the formation of carbon dust in hot environments where the C/O ratio is less than 1. We show that the fully mixed ejecta of a 170 M sun progenitor synthesizes 11.3 M sun of molecules, whereas 20 M sun and 270 M sun progenitors produce 0.78 M sun and 3.2 M sun of molecules, respectively. The admixing of 10% of hydrogen into the fully mixed ejecta of the 170 M sun progenitor increases its molecular yield to ∼47 M sun . The unmixed ejecta of a 170 M sun progenitor SN without hydrogen penetration synthesizes ∼37 M sun of molecules, whereas its 20 M sun counterpart produces ∼1.2 M sun . This smaller efficiency at forming molecules is due to the large fraction of He + in the

Determination of water saturation in subsurface earth formations adjacent well boreholes

International Nuclear Information System (INIS)

Scott, Hubert D.

1982-01-01

There is provided a method of determining the water saturation of an earth formation surrounding a well borehole, comprising the steps of: (a) bombarding the earth formation with repetitive pulses of fast neutrons which are slowed down and thereafter engage in neutron capture reactions with materials in the vicinity of the borehole; (b) obtaining by use of a germanium gamma ray detector gamma ray spectra of the materials in the vicinity of the borehole; (c) obtaining from the gamma ray spectra a measure of the relative presence of chlorine to that of hydrogen in the formation; (d) obtaining a measure of apparent formation water salinity from the measure of relative presence of chlorine to hydrogen in the formation; and (e) obtaining the water saturation of the formation utilizing the apparent formation water salinity

Effect of water flow rate and water chemistry on corrosion environment in reactor pressure vessel bottom of BWRs

Energy Technology Data Exchange (ETDEWEB)

Ichikawa, Nagayoshi; Hemmi, Yukio; Takagi, Junichi; Urata, Hidehiro [Toshiba Corp., Kawasaki, Kanagawa (Japan)

1999-07-01

To evaluate the corrosion environment at the bottom of the reactor pressure vessel in a BWR and the effect of hydrogen water chemistry on the corrosion of materials in the region, measurements of the corrosion potential of Type-304 stainless steel and nickel base alloy were made in a laboratory test loop. The effect of water chemistry on the corrosion potential of nickel base alloy is found to be similar to the effect on Type-304 stainless steel. Flow analysis and precise evaluations of the corrosion potential of materials in the bottom region were implemented. Corrosion potentials throughout the region were evaluated from the flow analysis results. At the jet pump outlet and shroud support leg, a rather large amount of hydrogen had to be added to reduce the potential. Conversely, a small amount of hydrogen was enough in the case of the stub tube of the control rod drive guide tubing and the ICM housings located in the center of the bottom region. (author)

Effect of water flow rate and water chemistry on corrosion environment in reactor pressure vessel bottom of BWRs

International Nuclear Information System (INIS)

Ichikawa, Nagayoshi; Hemmi, Yukio; Takagi, Junichi; Urata, Hidehiro

1999-01-01

To evaluate the corrosion environment at the bottom of the reactor pressure vessel in a BWR and the effect of hydrogen water chemistry on the corrosion of materials in the region, measurements of the corrosion potential of Type-304 stainless steel and nickel base alloy were made in a laboratory test loop. The effect of water chemistry on the corrosion potential of nickel base alloy is found to be similar to the effect on Type-304 stainless steel. Flow analysis and precise evaluations of the corrosion potential of materials in the bottom region were implemented. Corrosion potentials throughout the region were evaluated from the flow analysis results. At the jet pump outlet and shroud support leg, a rather large amount of hydrogen had to be added to reduce the potential. Conversely, a small amount of hydrogen was enough in the case of the stub tube of the control rod drive guide tubing and the ICM housings located in the center of the bottom region. (author)

Natural Pathogen Control Chemistry to Replace Toxic Treatment of Microbes and Biofilm in Cooling Towers

Science.gov (United States)

Brouse, Lon; Brouse, Richard; Brouse, Daniel

2017-01-01

Application of toxic antibacterial agents is considered necessary to control prevalent fresh water microorganisms that grow in evaporative cooling water systems, but can adversely affect the environment and human health. However, natural antibacterial water chemistry has been applied in industrial cooling water systems for over 10 years to inhibit microorganisms with excellent results. The water chemistry method concentrates natural minerals in highly-softened water to produce elevated pH and dissolved solids, while maintaining low calcium and magnesium content. The method provides further benefits in water conservation, and generates a small volume of non-toxic natural salt concentrate for cost efficient separation and disposal if required. This report describes the antimicrobial effects of these chemistry modifications in the cooling water environment and the resultant collective inhibition of microbes, biofilm, and pathogen growth. This article also presents a novel perspective of parasitic microbiome functional relationships, including “Trojan Protozoans” and biofilms, and the function of polyvalent metal ions in the formation and inhibition of biofilms. Reducing global dependence on toxic antibacterial agents discharged to the environment is an emerging concern due to their impact on the natural microbiome, plants, animals and humans. Concurrently, scientists have concluded that discharge of antibacterial agents plays a key role in development of pathogen resistance to antimicrobials as well as antibiotics. Use of natural antibacterial chemistry can play a key role in managing the cooling water environment in a more ecologically sustainable manner. PMID:28420074

Chemistry which created Green River Formation oil shale

Energy Technology Data Exchange (ETDEWEB)

Smith, J.W.

1983-01-01

The genesis pattern presented for Green River Formation oil shale explains the major observation. Deposition of relatively large quantities of hydrogen-rich organic matter in the oil shales is a natural consequence of the chemical conditions (basic water and reducing atmosphere) and the physical limitation of clastic materials developed in the stratified ancient Lake Uinta. Stability of the stratification produced the continuous deposition of the organic matter and its uniformity over the deposit. Authigenic formation of the oil-shale minerals proceeds naturally from the lake stratification, and the varve production stems from the seasonable development of organic matter. The lake's stratification produced uniform deposition over the entire area it covered, making the correlatable lateral persistence of the thin laminations a natural consequence. As the lake developed, the attack on aluminosilicates by sodium carbonate in the lower layer produced a silicate skeleton protected by aluminum trihydroxide. On deposition, this aluminum-rich skeleton formed illite in quantity. As the lake became more basic, the protecting aluminum hydroxide coating dissolved amphoterically and illite production dropped at a specific point. Continual build-up of sodium carbonate and aluminate ion in the water of the lake's lower layer reached conditions which precipitated dawsonite and crystallized nahcolite in the sediment as a result of CO/sub 2/ production from organic matter. (JMT)

Advanced studies in chemistry control with morpholine

International Nuclear Information System (INIS)

Riddle, J.M.

1992-07-01

Prior studies at Beaver Valley Unit 1 and at Prairie Island found that the substitution of morpholine for ammonia reduced corrosion and iron transport in the feedtrain of pressurized water reactors. The benefits of using morpholine encouraged other utilities to consider morpholine water chemistry. Calvert Cliffs Unit 1 was the first domestic PWR with deep-bed condensate polishers to use morpholine water chemistry. Typically a bed is operated in the hydrogen cycle for eight to ten days, followed by an additional 25 days in the morpholine cycle. Morpholine reduced feedwater iron levels by 28 percent. With morpholine treatment at Calvert Cliffs Unit 1, corrosion product transport in feedwater was reduced by a factor of 1.3 -- 1.4. Morpholine treatment at higher levels at Prairie Island Unit 2 provided a factor of 2.3 reduction in feedwater iron transport, in agreement with data from Electricity de France. EdF data show that the factor increases as the pH for ammonia chemistry is reduced from 9.5. When possible, the factors were compared at a pH of 9.2 for morpholine at room temperature. Aqueous solutions of morpholine thermally decompose at increasing rates with temperature above about 288 degree C (550 degree F). Oxygen and several metal oxides appear to increase the rate of decomposition to a small extent. Acetate, formate, and various amines, including ammonia, are the principal decomposition products

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.

Role of aldehyde chemistry and NOx concentrations in secondary organic aerosol formation

Directory of Open Access Journals (Sweden)

P. O. Wennberg

2010-08-01

Full Text Available Aldehydes are an important class of products from atmospheric oxidation of hydrocarbons. Isoprene (2-methyl-1,3-butadiene, the most abundantly emitted atmospheric non-methane hydrocarbon, produces a significant amount of secondary organic aerosol (SOA via methacrolein (a C4-unsaturated aldehyde under urban high-NOx conditions. Previously, we have identified peroxy methacryloyl nitrate (MPAN as the important intermediate to isoprene and methacrolein SOA in this NOx regime. Here we show that as a result of this chemistry, NO2 enhances SOA formation from methacrolein and two other α, β-unsaturated aldehydes, specifically acrolein and crotonaldehyde, a NOx effect on SOA formation previously unrecognized. Oligoesters of dihydroxycarboxylic acids and hydroxynitrooxycarboxylic acids are observed to increase with increasing NO2/NO ratio, and previous characterizations are confirmed by both online and offline high-resolution mass spectrometry techniques. Molecular structure also determines the amount of SOA formation, as the SOA mass yields are the highest for aldehydes that are α, β-unsaturated and contain an additional methyl group on the α-carbon. Aerosol formation from 2-methyl-3-buten-2-ol (MBO232 is insignificant, even under high-NO2 conditions, as PAN (peroxy acyl nitrate, RC(OOONO2 formation is structurally unfavorable. At atmospherically relevant NO2/NO ratios (3–8, the SOA yields from isoprene high-NOx photooxidation are 3 times greater than previously measured at lower NO2/NO ratios. At sufficiently high NO2 concentrations, in systems of α, β-unsaturated aldehydes, SOA formation from subsequent oxidation of products from acyl peroxyl radicals+NO2 can exceed that from RO2+HO2 reactions under the same inorganic seed conditions, making RO2+NO2 an important channel for SOA formation.

Role of aldehyde chemistry and NOx concentrations in secondary organic aerosol formation

Science.gov (United States)

Chan, A. W. H.; Chan, M. N.; Surratt, J. D.; Chhabra, P. S.; Loza, C. L.; Crounse, J. D.; Yee, L. D.; Flagan, R. C.; Wennberg, P. O.; Seinfeld, J. H.

2010-08-01

Aldehydes are an important class of products from atmospheric oxidation of hydrocarbons. Isoprene (2-methyl-1,3-butadiene), the most abundantly emitted atmospheric non-methane hydrocarbon, produces a significant amount of secondary organic aerosol (SOA) via methacrolein (a C4-unsaturated aldehyde) under urban high-NOx conditions. Previously, we have identified peroxy methacryloyl nitrate (MPAN) as the important intermediate to isoprene and methacrolein SOA in this NOx regime. Here we show that as a result of this chemistry, NO2 enhances SOA formation from methacrolein and two other α, β-unsaturated aldehydes, specifically acrolein and crotonaldehyde, a NOx effect on SOA formation previously unrecognized. Oligoesters of dihydroxycarboxylic acids and hydroxynitrooxycarboxylic acids are observed to increase with increasing NO2/NO ratio, and previous characterizations are confirmed by both online and offline high-resolution mass spectrometry techniques. Molecular structure also determines the amount of SOA formation, as the SOA mass yields are the highest for aldehydes that are α, β-unsaturated and contain an additional methyl group on the α-carbon. Aerosol formation from 2-methyl-3-buten-2-ol (MBO232) is insignificant, even under high-NO2 conditions, as PAN (peroxy acyl nitrate, RC(O)OONO2) formation is structurally unfavorable. At atmospherically relevant NO2/NO ratios (3-8), the SOA yields from isoprene high-NOx photooxidation are 3 times greater than previously measured at lower NO2/NO ratios. At sufficiently high NO2 concentrations, in systems of α, β-unsaturated aldehydes, SOA formation from subsequent oxidation of products from acyl peroxyl radicals+NO2 can exceed that from RO2+HO2 reactions under the same inorganic seed conditions, making RO2+NO2 an important channel for SOA formation.

Water regime of steam power plants

International Nuclear Information System (INIS)

Oesz, Janos

2011-01-01

The water regime of water-steam thermal power plants (secondary side of pressurized water reactors (PWR); fossil-fired thermal power plants - referred to as steam power plants) has changed in the past 30 years, due to a shift from water chemistry to water regime approach. The article summarizes measures (that have been realised by chemists of NPP Paks) on which the secondary side of NPP Paks has become a high purity water-steam power plant and by which the water chemistry stress corrosion risk of heat transfer tubes in the VVER-440 steam generators was minimized. The measures can also be applied to the water regime of fossil-fired thermal power plants with super- and subcritical steam pressure. Based on the reliability analogue of PWR steam generators, water regime can be defined as the harmony of construction, material(s) and water chemistry, which needs to be provided in not only the steam generators (boiler) but in each heat exchanger of steam power plant: - Construction determines the processes of flow, heat and mass transfer and their local inequalities; - Material(s) determines the minimal rate of general corrosion and the sensitivity for local corrosion damage; - Water chemistry influences the general corrosion of material(s) and the corrosion products transport, as well as the formation of local corrosion environment. (orig.)

Experimental proposals for procedures to investigate the water chemistry, sorption and transport properties of marl

International Nuclear Information System (INIS)

Bradbury, M.H.; Baeyens, B.; Alexander, W.R.

1990-11-01

The aim of this report is to describe a framework within which laboratory studies on groundwater chemistry, sorption and transport properties might be conducted on samples from rock formations being considered as potential 'host rocks' for the disposal of radioactive waste. Here, Valanginian marl, has been taken as a specific example, but the general principles should be applicable to other systems. Some brief notes are given on sampling and handling procedures and mineralogical characterisation. This is followed by a detailed discussion of the procedures considered necessary to determine a groundwater chemistry of a specific rock matrix. The methods described are particularly appropriate to rocks such as marl i.e. low water content rocks (essentially 'dry') with appreciable clay and carbonate contents. An important conclusion drawn is that simple aqueous phase extractions at different liquid to solid ratios, followed by extrapolation procedures, are not always appropriate and can lead to incorrect water compositions. Some of the uncertainties and difficulties inherently involved in determining sorption parameters from batch, infiltration and diffusion based methods are presented. These methods are then individually discussed in greater detail with some illustrative examples. In the relatively few studies where sorption has been measured in crushed rock tests and compared with the results from intact rock experiments, it is often found that there are discrepancies. An outline for an experiment is described in which results from the two types of test could be quantitatively related to one another via cation exchange capacity measurements. Using this method it might be possible to explain the reasons for such discrepancies. Finally, a brief discussion is given on the possible consequences for experimental studies of gas in Valanginian marl and the swelling of the clay rich components. (author) 8 figs., 4 tabs., 46 refs

Optimum coolant chemistry in BWRs

International Nuclear Information System (INIS)

Lin, C.C.; Cowan, R.L.; Kiss, E.

2004-01-01

LWR water chemistry parameters are directly or indirectly related to the plant's operational performance and for a significant amount of Operation and Maintenance (O and M) costs. Obvious impacts are the operational costs associated with water treatment, monitoring and associated radwaste generation. Less obvious is the important role water chemistry plays in the magnitude of drywell shutdown dose rates, fuel corrosion performance and, (probably most importantly) materials degradation such as from stress corrosion cracking of piping and Reactor Pressure Vessel (RPV) internal components. To improve the operational excellence of the BWR and to minimize the impact of water chemistry on O and M costs. General Electric has developed the concept of Optimum Water Chemistry (OWC). The 'best practices' and latest technology findings from the U.S., Asia and Europe are integrated into the suggested OWC Specification. This concept, together with cost effective ways to meet the requirement, are discussed. (author)

The Environmental Impact of Oilfield Formation Water on a ...

African Journals Online (AJOL)

A comparative analysis of the physico-chemical parameters of treated oilfield formation water and that of a freshwater stream with no previous history of pollution from oil exploration activities was determined. The environmental impact resulting from the discharge of treated oilfield formation water into freshwater samples ...

Seasonal change in precipitation, snowpack, snowmelt, soil water and streamwater chemistry, northern Michigan

Science.gov (United States)

Stottlemyer, R.; Toczydlowski, D.

1999-01-01

We have studied weekly precipitation, snowpack, snowmelt, soil water and streamwater chemistry throughout winter for over a decade in a small (176 ha) northern Michigan watershed with high snowfall and vegetated by 60 to 80 year-old northern hardwoods. In this paper, we examine physical, chemical, and biological processes responsible for observed seasonal change in streamwater chemistry based upon intensive study during winter 1996-1997. The objective was to define the contributions made to winter and spring streamwater chemical concentration and flux by processes as snowmelt, over-winter forest floor and surface soil mineralization, immobilization, and exchange, and subsurface flowpath. The forest floor and soil were unfrozen beneath the snowpack which permitted most snowmelt to enter. Over-winter soil mineralization and other biological processes maintain shallow subsurface ion and dissolved organic carbon (DOC) reservoirs. Small, but steady, snowmelt throughout winter removed readily mobilized soil NO3- which resulted in high over-winter streamwater concentrations but little flux. Winter soil water levels and flowpaths were generally deep which increased soil water and streamwater base cation (C(B)), HCO3-, and Si concentrations. Spring snowmelt increased soil water levels and removal of ions and DOC from the biologically active forest floor and shallow soils. The snowpack solute content was a minor component in determining streamwater ion concentration or flux during and following peak snowmelt. Exchangeable ions, weakly adsorbed anions, and DOC in the forest floor and surface soils dominated the chemical concentration and flux in soil water and streamwater. Following peak snowmelt, soil microbial immobilization and rapidly increased plant uptake of limiting nutrients removed nearly all available nitrogen from soil water and streamwater. During the growing season high evapotranspiration increased subsurface flowpath depth which in turn removed weathering

Soil water and xylem chemistry in declining sugar maple stands in Pennsylvania

Science.gov (United States)

David R. DeWalle; Bryan R. Swistock; William E. Sharpe

1999-01-01

Evidence is accumulating that decline of sugar maple, Acer saccharum Marsh., in northern Pennsylvania may be related to overall site fertility as reflected in the chemistry of soil water and bolewood xylem. In this paper we discuss factors related to varying site fertility, including effects of soil liming, past glacialion, topographic position and...

Gas-phase hydrolysis of triplet SO2: A possible direct route to atmospheric acid formation

Science.gov (United States)

Donaldson, D. James; Kroll, Jay A.; Vaida, Veronica

2016-07-01

Sulfur chemistry is of great interest to the atmospheric chemistry of several planets. In the presence of water, oxidized sulfur can lead to new particle formation, influencing climate in significant ways. Observations of sulfur compounds in planetary atmospheres when compared with model results suggest that there are missing chemical mechanisms. Here we propose a novel mechanism for the formation of sulfurous acid, which may act as a seed for new particle formation. In this proposed mechanism, the lowest triplet state of SO2 (3B1), which may be accessed by near-UV solar excitation of SO2 to its excited 1B1 state followed by rapid intersystem crossing, reacts directly with water to form H2SO3 in the gas phase. For ground state SO2, this reaction is endothermic and has a very high activation barrier; our quantum chemical calculations point to a facile reaction being possible in the triplet state of SO2. This hygroscopic H2SO3 molecule may act as a condensation nucleus for water, giving rise to facile new particle formation (NPF).

Experimental interstellar organic chemistry: Preliminary findings

Science.gov (United States)

Khare, B. N.; Sagan, C.

1971-01-01

In a simulation of interstellar organic chemistry in dense interstellar clouds or on grain surfaces, formaldehyde, water vapor, ammonia and ethane are deposited on a quartz cold finger and ultraviolet-irradiated in high vacuum at 77K. The HCHO photolytic pathway which produces an aldehyde radical and a superthermal hydrogen atom initiates solid phase chain reactions leading to a range of new compounds, including methanol, ethanol, acetaldehyde, acetonitrile, acetone, methyl formate, and possibly formic acid. Higher nitriles are anticipated. Genetic relations among these interstellar organic molecules (e.g., the Cannizzaro and Tischenko reactions) must exist. Some of them, rather than being synthesized from smaller molecules, may be degradation products of larger organic molecules, such as hexamethylene tetramine, which are candidate consitituents of the interstellar grains. The experiments reported here may also be relevant to cometary chemistry.

Formation of brominated trihalomethanes in chlorinated drinking-water from Lake Constance

International Nuclear Information System (INIS)

Petri, M.; Stabel, H.H.

1994-01-01

The formation of trihalomethanes (THMs) in raw water and drinking water from Lake Constance containing low amounts of DOC and bromide was studied with special emphasis on brominated trihalomethanes (Br-THMs). If the raw water was ozonated prior to chlorination, the formation of THMs was reduced by 37%, and if a rapid sandfiltration was interposed, the THM-formation was again slightly enhanced. The percentage of Br-THMs on total-THMs increased from 16% to 35% during the treatment process. In the drinking water distribution system of BWV the formation of Br-THMs and CHCl 3 was studied with respect to residence time and post-chlorination. Unless the post-chlorination was performed, the THM-formation in the distribution system resembled that obtained from laboratory studies, except for small amounts of THMs being purged due to transport in the mains and residence in the reservoirs. Post-chlorination increased CHCl 3 - and the CHBrCl 2 -formation, but there was no effect on the formation of CHBr 2 Cl and CHBr 3 . However, the total THM-concentration in the drinking water never exceeded the German drinking water standard of 10 μg/L. (orig.) [de

Characterization of Formation Water Constituents and the Effect of ...

African Journals Online (AJOL)

Michael Horsfall

ABSTRACT: The research work examined the constituents of formation water and fresh water dilution effects from a land location in the Niger Delta Area of Nigeria. Some selected physicochemical and microbiological analyses were determined at ambient temperature (82oF) and formation temperature (185oF). Analysis of ...

Water chemistry and soil radon survey at the Poas volcano (Costa Rica

Directory of Open Access Journals (Sweden)

J. L. Seidel

2005-06-01

Full Text Available Radon-in-soil monitoring at the Poas volcano (Costa Rica has been performed together with water chemistry from the hot crater lake since 1981 and 1983 respectively. The results are discussed as a function of the eruptive evolution of the volcano over a 13 years period (1981-1994. It is shown that no definitely clear precursory radon signals have been recorded. On the contrary, ionic species concentrations are likely to be considered good precursors, together with the temperature variations of the crater lake water.

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.

Geochemical of clay formations : study of Spanish clay REFERENCE

International Nuclear Information System (INIS)

Turrero, M. J.; Pena, J.

2003-01-01

Clay rocks are investigated in different international research programs in order to assess its feasibility for the disposal of high level radioactive wastes. This is because different sepcific aspects: they have low hydraulic conductivity (10''-11-10''-15 m/s), a high sorption capacity, self-sealing capacity of facults and discontinuities and mechanical resistance. Several research programs on clay formations are aimed to study the chemistry of the groundwater and the water-rock reactions that control it: e. g. Boom Clay (Mol, Belgium), Oxford Clay /Harwell, United Kingdom), Toarcian Clay (Tournemire, France), Palfris formation (Wellenberg, Switzerland), Opalinus Clay (Bure, France). Based on these studies, considerable progress in the development of techniques for hydrologic, geochemical and hydrogeochemical characterization of mudstones has been accomplished (e. g. Beaufais et al. 1994, De Windt el al. 1998. Thury and Bossart 1999, Sacchi and Michelot 2000) with important advances in the knowledge of geochemical process in these materials (e. g. Reeder et al. 1993, Baeyens and Brandbury 1994, Beaucaire et al. 2000, Pearson et al., 2003).Furtermore, geochemical modeling is commonly used to simulate the evolution of water chemistry and to understand quantitatively the processes controlling the groundwater chemistry (e. g. Pearson et al. 1998, Tempel and Harrison 2000, Arcos et al., 2001). The work presented here is part of a research program funded by Enresa in the context of its R and D program. It is focused on the characterization of a clay formation (reference Argillaceous Formation, RAF) located within the Duero Basin (north-centralSpain). The characterisation of th ephysical properties,, fluid composition, mineralogy, water-rock reaction processes, geochemical modelling and sorption properties of the clays from the mentioned wells is the main purpose of this work. (Author)

Solvent extraction: the coordination chemistry behind extractive metallurgy.

Science.gov (United States)

Wilson, A Matthew; Bailey, Phillip J; Tasker, Peter A; Turkington, Jennifer R; Grant, Richard A; Love, Jason B

2014-01-07

The modes of action of the commercial solvent extractants used in extractive hydrometallurgy are classified according to whether the recovery process involves the transport of metal cations, M(n+), metalate anions, MXx(n-), or metal salts, MXx into a water-immiscible solvent. Well-established principles of coordination chemistry provide an explanation for the remarkable strengths and selectivities shown by most of these extractants. Reagents which achieve high selectivity when transporting metal cations or metal salts into a water-immiscible solvent usually operate in the inner coordination sphere of the metal and provide donor atom types or dispositions which favour the formation of particularly stable neutral complexes that have high solubility in the hydrocarbons commonly used in recovery processes. In the extraction of metalates, the structures of the neutral assemblies formed in the water-immiscible phase are usually not well defined and the cationic reagents can be assumed to operate in the outer coordination spheres. The formation of secondary bonds in the outer sphere using, for example, electrostatic or H-bonding interactions are favoured by the low polarity of the water-immiscible solvents.

Alternative water chemistry for the primary loop of PWR plants

Energy Technology Data Exchange (ETDEWEB)

Henzel, N [Siemens AG Unternehmensbereich KWU, Erlangen (Germany)

1997-02-01

Advanced fuel element concepts (longer cycles, higher burnup, increased rod power) call for more reactivity binding capacity and, moreover, might produce higher void fractions, particularly in the hot channel. Thus, on the one hand, more alcalizing agent is needed to maintain a high coolant pH according to the approved ``modified boron-lithium mode of operation`` in the presence of more boric acid (chemical shim); on the other hand, increasing enrichment of coolant constituents due to local boiling (higher void fraction), which must not result in accelerated corrosion of fuel cladding and structural materials, imposes enhanced requirements on both, materials technology and water chemistry. At present, the use of boric acid enriched in B10 (the isotope effective in terms of reactivity control) appears to advantageously compromise in capturing more neutrons with less total boron while maintaining or even slightly reducing lithium concentrations at the same time. There is no feasible alternative for boric acid used as the chemical shim and for hydrogen gas as the reducing agent used to suppress oxygen formation by water radiolysis. Systematic screening as performed in phase 1 of a recent project proved potassium hydroxide to be the only potential candidate to favourably replace lithium 7 hydroxide as an alcalizing agent. Unfortunately, the results of pertinent comparative corrosion tests are not unambiguous, and available operational experience with potassium hydroxide in WWER plants is not readily applicable to western world-type PWR plants. Therefore, a switch-over from lithium to potassium can be envisaged only subsequent to a comprehensive qualification program which is planned to be the objective of phase 2 of the project. This program should also comprise zinc addition tests in order to confirm the alleged positive impact of this element on corrosion rates and activity buildup. (Abstract Truncated)

Predicting hydrocarbon potential of an earth formation underlying water

International Nuclear Information System (INIS)

Damaison, G.J.; Kaplan, I.R.

1981-01-01

A method for the on-site collection and examination of small concentrations of a carbonaceous gas, e.g. methane, dissolved in a body of water overlying an earth formation to predict hydrocarbon potential of the earth formation under the body of water, the formation being a source of carbonaceous gas, comprises at a known geographic location sampling the water at a selected flow rate and at a selected depth; continuously vacuum separating the water into liquid and gas phases; separating a selected carbonaceous gas from interfering gas species in the presence of an air carrier vented to atmosphere at a known flow rate; and quantitatively oxidizing the selected gas and then cryogenically trapping an oxidant thereof in the presence of said air carrier to provide for an accurate isotopic examination. (author)

Water chemistry experience following an extensive power up-rate in Oskarshamn 3 BWR

International Nuclear Information System (INIS)

Wegemar, Boerje; Nilsson, Jimmy; Lejon Johan; Bergfors, Asa; Arnberg, Bo

2012-09-01

The Swedish Oskarshamn 3 BWR plant, operated by OKG, was first connected to the grid in 1985. The plant has been power up-rated in two steps; from the original design, 3020 MWth, to 3300 MWth (109%, 1989) and recently to 3900 MWth (129%, 2009). Westinghouse Electric Sweden AB (former ASEA-Atom, OEM of the plant) was rewarded a major contract in the recently implemented up-rating project, the PULS project. The PULS project is quite unique since no operating experience has to date been reported from a similar major power up-rate in a BWR plant. Water chemistry experience from the first period of operation following the implementation of the PULS project is reported and discussed in the paper. Reported chemistry and radiochemistry measurements in feedwater (FW) and reactor water (RW) include corrosion products, activated corrosion products, dissolved oxygen and impurities like chloride, sulfate etc. Furthermore, a comparison of water quality prior to implementation of the PULS project is included. Several process systems have been modified, one of them being the condensate cleanup system (CCU), a Pre-coat filter system. The design criteria for the CCU system include the filter run-lengths, pressure drop before back-washing and requirements on water chemistry quality. The paper describes in some detail the CCU system modifications being implemented in order to fulfil the design criterion. CCU cleanup efficiency, operating temperature and influence of hydrogen peroxide on the CCU resin are all important issues being covered in the paper. As for the latter, it is well known that oxygen and hydrogen peroxide (from radiolysis in the core region) might cause partial deterioration of CCU standard cation resin resulting in increased RW sulfate concentrations. This aspect is covered in the paper as well. The reactor water cleanup system (RWCU) in Oskarshamn 3 consists of deep bed ion exchange filters (mixed bed filter). The purpose of RWCU is to maintain a low level of

BWR and PWR chemistry operating experience and perspectives

International Nuclear Information System (INIS)

Fruzzetti, K.; Garcia, S.; Lynch, N.; Reid, R.

2014-01-01

It is well recognized that proper control of water chemistry plays a critical role in ensuring the safe and reliable operation of Boiling Water Reactors (BWRs) and Pressurized Water Reactors (PWRs). State-of-the-art water chemistry programs reduce general and localized corrosion of reactor coolant system, steam cycle equipment, and fuel cladding materials; ensure continued integrity of cycle components; and reduce radiation fields. Once a particular nuclear plant component has been installed or plant system constructed, proper water chemistry provides a global tool to mitigate materials degradation problems, thereby reducing the need for costly repairs or replacements. Recognizing the importance of proper chemistry control and the value in understanding the relationship between chemistry guidance and actual operating experience, EPRI continues to collect, monitor, and evaluate operating data from BWRs and PWRs around the world. More than 900 cycles of valuable BWR and PWR operating chemistry data has been collected, including online, startup and shutdown chemistry data over more than 10 years (> 20 years for BWRs). This paper will provide an overview of current trends in BWR and PWR chemistry, focusing on plants in the U.S.. Important chemistry parameters will be highlighted and discussed in the context of the EPRI Water Chemistry Guidelines requirements (i.e., those parameters considered to be of key importance as related to the major goals identified in the EPRI Guidelines: materials integrity; fuel integrity; and minimizing plant radiation fields). Perspectives will be provided in light of recent industry initiatives and changes in the EPRI BWR and PWR Water Chemistry Guidelines. (author)

On 2D water chemistry

International Nuclear Information System (INIS)

Shimkevich, Alexander; Shimkevich, Inessa

2012-09-01

The micro-structural behaviour of density fluctuations in liquid water shows that the hydrogen-bonds lifetime is 1-20 ps whereas the broken-bonds lifetime is about 0.1 ps. Therefore spontaneously broken bonds will probably reform to give the original hydrogen bond configuration, but their coherent breakage in molecular cluster will lead to rotation of water molecules around the remaining hydrogen bonds. Our model for topological structure of dense part of liquid water in its density fluctuations as helical tetrahedral clusters is useful for explanation of liquid-water structural anomalies including the high quantity of hydrogen bonds with tetrahedral orientation in non-ordered liquid matrix. The topology of such the clusters is essentially differed from topology of crystalline ice. From this and only this point of view, water can be considered as a two-structural liquid because the formation and decay of such the clusters has dynamic character and is natural consequence of condensed-matter density fluctuations. At a hydrogen-steam (or oxygen-steam) mixture is injected in aqueous solution, it is possible to obtain the stable gaseous nano-bubbles. Such the nano-fluid can convert the liquid water in the non-stoichiometric state, H 2 O 1 ± z , and (without impurity addition) change its Reduction-Oxidation (Redox) potential. In this connection, we offer to use Fermi level of electron energy in the aqueous solution for correct expressing Redox potential of non-stoichiometric water. If Fermi level will be about in the middle of the band gap, the average number of electrons per quantum state of a reducing agent will be zero and the same factor for the oxidizing one will be unity that is the chemical activity of these agents will be zero. At the same time, the liquid-water non-stoichiometric composition, H 2 O 1 ± z , is varied in the very narrow range of z ≤ 10 -6 . Therefore it is important monitoring the Redox potential (Fermi level) online by precise sensor having

On the chemistry of the lightest exotic atoms

International Nuclear Information System (INIS)

Horvath, D.

1980-01-01

The chemical aspects of formation of three hydrogen-like exotic atoms, positronium, muonium and pionic hydrogen are discussed. For positronium two formation mechanisms, the Ore model with hot-atom reactions, and the spur reaction model are set against experimental observations in solutions. The use of pionic hydrogen atoms in obtaining information on the bond properties of hydrogen is illustrated by recent experiments performed in JINR. The use of negative pions in chemistry is demonstrated by electronic structure investigations performed in Dubna. The probability W that in a chemical system containing bound hydrogen atoms a stopped negative pion is captured by a proton reflects the bond properties of hydrogen. Recent results haVe shown that the hydrogen bond formation in liquid water and the coordination of water molecules in aquacomplexes lead to significant decreases in probability W for water. A comparison of the chemical uses of the exotic atoms shows that positronium and muonium inform us on intermolecular level probing a small environment of a few molecules while the pionic hydrogen atoms deliver information on the chemical bond of hydrogen, i.e. on intramolecular level

Influence of hydrazine primary water chemistry on corrosion of fuel cladding and primary circuit components

International Nuclear Information System (INIS)

Iourmanov, V.; Pashevich, V.; Bogancs, J.; Tilky, P.; Schunk, J.; Pinter, T.

1999-01-01

Earlier at Paks 1-4 NPP standard ammonia chemistry was in use. The following station performance indicators were improved when hydrazine primary water chemistry was introduced: occupational radiation exposures of personnel; gamma-radiation dose rates near primary system components during refuelling and maintenance outages. The reduction of radiation exposures and radiation fields were achieved without significant expenses. Recent results of experimental studies allowed to explain the mechanism of hydrazine dosing influence on: corrosion rate of structure materials in primary coolant; behaviour of soluble and insoluble corrosion products including long-life corrosion-induced radionuclides in primary system during steady-state and transient operation modes; radiolytic generation of oxidising radiolytic products in core and its corrosion activity in primary system; radiation situation during refuelling and maintenance outages; foreign material degradation and removal (including corrosion active oxidant species) from primary system during abnormal events. Operational experience and experimental data have shown that hydrazine primary water chemistry allows to reduce corrosion wear and thereby makes it possible to extend the life-time of plant components in primary system. (author)

Water Transfer Characteristics during Methane Hydrate Formation Processes in Layered Media

Directory of Open Access Journals (Sweden)

Yousheng Deng

2011-08-01

Full Text Available Gas hydrate formation processes in porous media are always accompanied by water transfer. To study the transfer characteristics comprehensively, two kinds of layered media consisting of coarse sand and loess were used to form methane hydrate in them. An apparatus with three PF-meter sensors detecting water content and temperature changes in media during the formation processes was applied to study the water transfer characteristics. It was experimentally observed that the hydrate formation configurations in different layered media were similar; however, the water transfer characteristics and water conversion ratios were different.

Ground water chemistry and water-rock interaction at Kivetty

International Nuclear Information System (INIS)

Pitkaenen, P.; Leino-Forsman, H.

1992-10-01

The geochemistry of the groundwater at one of the investigation areas for nuclear waste, Kivetty (Kongingas) in central Finland is evaluated. The hydrogeological data is collected from boreholes drilled down to 1000-m depth into crystalline bedrock. The interpretation is based on groundwater chemistry and isotope data, mineralogical data and the structure and hydrology of the bedrock, using correlation diagrams and thermodynamic calculations (PHREEQE). The hydrogeochemistry and major processes controlling the groundwater chemistry are discussed

Relative effect of solder flux chemistry on the humidity related failures in electronics

DEFF Research Database (Denmark)

Verdingovas, Vadimas; Jellesen, Morten Stendahl; Ambat, Rajan

2015-01-01

Purpose - This paper aims to investigate the effect of no-clean flux chemistry with various weak organic acids (WOAs) as activators on the corrosion reliability of electronics with emphasis on the hygroscopic nature of the residue. Design/methodology/approach - The hygroscopicity of flux residue...... in the impedance measurements were observed. Practical implications - The findings are attributed to the deliquescence RH of the WOA(s) in the flux and chemistry of water-layer formation. The results show the importance of WOA type in relation to its solubility and deliquescence RH on the corrosion reliability...

NDMA formation during drinking water treatment: A multivariate analysis of factors influencing formation.

Science.gov (United States)

Leavey-Roback, Shannon L; Sugar, Catherine A; Krasner, Stuart W; Suffet, Irwin H Mel

2016-05-15

The formation of the carcinogen N-nitrosodimethylamine (NDMA) during drinking water treatment has raised concerns in the drinking water industry. Many bench-scale laboratory tests and pilot plant studies have been completed to try to determine which factors during water treatment increase or decrease the amount of NDMA formed in drinking water. This study used data from over 20 drinking water treatment plants in the United States and Canada to determine which factors are most highly correlated with the NDMA concentration in delivered water using a mixed effects model with a random intercept. This type of analysis has not been used previously with trihalomethane (THM) models due to the fact that those studies did not sample such a large number and range of plants as was done in this NDMA study. Ultraviolet absorbance at 254 nm (UV254) in the plant influent and pre-chlorination time used at the plant were highly correlated in all models with NDMA concentration in finished water as well as the percentage change between NDMA formation potential in the plant influent and actual formation in the finished water. Specifically, an increase in UV254 absorbance in a model was associated with an increase in NDMA and an increase in pre-chlorination time in a model was associated with a decrease in NDMA. Other water quality parameters including sucralose concentration in the plant influent, polyDADMAC polymer dose, pH, and chlorine-to-ammonia weight ratio used in the plant were also correlated with NDMA concentration in the distribution system. Lastly, NDMA precursor loading was correlated with the use of polyDADMAC (where precursors were added) and the use of ozone and granular activated carbon (GAC) treatment (where precursors were removed). Copyright © 2016 Elsevier Ltd. All rights reserved.

Numerical simulation of water and sand blowouts when penetrating through shallow water flow formations in deep water drilling

Science.gov (United States)

Ren, Shaoran; Liu, Yanmin; Gong, Zhiwu; Yuan, Yujie; Yu, Lu; Wang, Yanyong; Xu, Yan; Deng, Junyu

2018-02-01

In this study, we applied a two-phase flow model to simulate water and sand blowout processes when penetrating shallow water flow (SWF) formations during deepwater drilling. We define `sand' as a pseudo-component with high density and viscosity, which can begin to flow with water when a critical pressure difference is attained. We calculated the water and sand blowout rates and analyzed the influencing factors from them, including overpressure of the SWF formation, as well as its zone size, porosity and permeability, and drilling speed (penetration rate). The obtained data can be used for the quantitative assessment of the potential severity of SWF hazards. The results indicate that overpressure of the SWF formation and its zone size have significant effects on SWF blowout. A 10% increase in the SWF formation overpressure can result in a more than 90% increase in the cumulative water blowout and a 150% increase in the sand blowout when a typical SWF sediment is drilled. Along with the conventional methods of well flow and pressure control, chemical plugging, and the application of multi-layer casing, water and sand blowouts can be effectively reduced by increasing the penetration rate. As such, increasing the penetration rate can be a useful measure for controlling SWF hazards during deepwater drilling.

Theoretical chemistry in Belgium a topical collection from theoretical chemistry accounts

CERN Document Server

Champagne, Benoît; De Proft, Frank; Leyssens, Tom

2014-01-01

Readers of this volume can take a tour around the research locations in Belgium which are active in theoretical and computational chemistry. Selected researchers from Belgium present research highlights of their work. Originally published in the journal Theoretical Chemistry Accounts, these outstanding contributions are now available in a hardcover print format. This volume will be of benefit in particular to those research groups and libraries that have chosen to have only electronic access to the journal. It also provides valuable content for all researchers in theoretical chemistry.

Chemistry of Technetium

International Nuclear Information System (INIS)

Omori, Takashi

2001-01-01

Since the late 1970's the coordination chemistry of technetium has been developed remarkably. The background of the development is obviously related to the use of technetium radiopharmaceuticals for diagnosis in nuclear medicine. Much attention has also been denoted to the chemical behavior of environmental 99 Tc released from reprocessing plants. This review covers the several aspects of technetium chemistry, including production of radioisotopes, analytical chemistry and coordination chemistry. In the analytical chemistry, separation of technetium, emphasizing chromatography and solvent extraction, is described together with spectrophotometric determination of technetium. In the coordination chemistry of technetium, a characteristic feature of the chemistry of Tc(V) complexes is referred from the view point of the formation of a wide variety of highly stable complexes containing the Tc=O or Tc≡N bond. Kinetic studies of the preparation of Tc(III) complexes using hexakis (thiourea) technetium(III) ion as a starting material are summarized, together with the base hydrolysis reactions of Tc(III), Tc(IV) and Tc(V) complexes. (author)

The development of a neutralizing amines based reagent for maintaining the water chemistry for medium and high pressures steam boilers

Science.gov (United States)

Butakova, M. V.; Orlov, K. A.; Guseva, O. V.

2017-11-01

An overview of the development for neutralizing amine based reagent for water chemistry of steam boilers for medium and high pressures was given. Total values of the neutralization constants and the distribution coefficients of the compositions selected as a main criteria for reagent composition. Experimental results of using this new reagent for water chemistry in HRSG of power plant in oil-production company are discussed.

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 groundwater chemistry along flow paths in the aquifer can be accounted for by small amounts of feldspar and calcite dissolution; goethite

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.

Seasonal Variation in Water Chemistry Parameters in the Clayburn - Willband Watershed, Abbotsford, British Columbia.

Science.gov (United States)

Gillies, S. L.; Marsh, S. J.; Peucker-Ehrenbrink, B.; Janmaat, A.; Bourdages, M.; Paulson, D.; Bogaerts, P.; Robertson, K.; Clemence, E.; Smith, S.; Yakemchuk, A.; Faber, A.

2017-12-01

Faculty and students from the University of the Fraser Valley (UFV) have conducted time series sampling of the Fraser River at Fort Langley and six Fraser Valley tributaries as a member of the Global Rivers Observatory (GRO, www.globalrivers.org) coordinated by Woods Hole Oceanographic Institution and Woods Hole Research Center. The Clayburn - Willband - Stoney watershed has become a focus of the sampling being conducted by faculty and students from the Geography and Biology Departments at UFV. Water chemistry data (water temperature, dissolved oxygen, conductivity, pH and turbidity) and samples (nutrients, major ions and bacteria) have been collected weekly from sites on these creeks. These watersheds are threatened by increasing urban development, increasing idustrial activity, and expansion of agricultural landuse within the watershed. Documenting the seasonal changes in the water chemistry as measured during the onset of the heavy fall and winter precipitation events, the wet and cool winters and springs, and the hot and dry summers will assist in attempts to protect these important salmon spawning streams from anthropogenic activity.

Application of hydrogen water chemistry to moderate corrosive circumstances around the reactor pressure vessel bottom of boiling water reactors

International Nuclear Information System (INIS)

Shunsuke Uchida; Eishi Ibe; Katsumi Ohsumi

1994-01-01

Application of hydrogen water chemistry to moderate corrosive circumstances is a promising approach to preserve structural integrities of major components and structures in the primary cooling system of BWRs. The benefits of HWC application are usually accompanied by several disadvantages. After evaluating merits and demerits of HWC application, it is concluded that optimal amounts of hydrogen injected into the feed water can moderate corrosive circumstances, in the region to be preserved, without serious disadvantages. (authors). 1 fig., 4 refs

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

International Nuclear Information System (INIS)

2012-01-01

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.

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.

Hydrogen water chemistry for BWRs: A status report on the EPRI development program