WorldWideScience

Sample records for removing water molecules

  1. STABILIZATION OF THE NEUTRAL PROTEASE OF BACILLUS-STEAROTHERMOPHILUS BY REMOVAL OF A BURIED WATER MOLECULE

    VRIEND, G; BERENDSEN, HJC; VANDERZEE, [No Value; VANDENBURG, B; VENEMA, G; EIJSINK, VGH

    1991-01-01

    Using site-directed mutagenesis, Ala166 in the neutral protease of Bacillus stearothermophilus was changed into Ser. Model building and molecular dynamics simulations of the mutant enzyme indicated that the Ser hydroxyl group fits well in a cavity which contains a water molecule in the wild-type

  2. Tar removal from biosyngas in the biomass gasification process. (Liquid + liquid) equilibrium {water + solvent (paraxylene and methyl hexadecanoate) + model molecules of tar (benzene, toluene, phenol)}

    Bassil, Georgio; Mokbel, Ilham; Abou Naccoul, Ramy; Stephan, Juliette; Jose, Jacques; Goutaudier, Christelle

    2012-01-01

    Highlights: ► (Liquid + liquid) equilibria at atmospheric pressure. ► Solubility of benzene (or toluene or phenol) in paraxylene at (303 to 343) K. ► Solubility of benzene (or toluene or phenol) in methyl palmitate or methyl hexadecanoate at (303 to 343) K. ► Correlation of LLE using NRTL model. - Abstract: Tar is generated in the process by the condensation of the gas resulting from biomass gasification. The objective of this work is a contribution to the database on thermodynamic quantity which will be useful at the operation of tar removal from aqueous medium. With this aim, (liquid + liquid) equilibrium of {water + solvent (paraxylene and methyl hexadecanoate) + model molecules of tar (benzene, toluene, phenol)} was studied at temperatures (303.2, 323.2, and 343.2) K. The data obtained were correlated with the non-random two-liquid (NRTL) model.

  3. Removing water from gels

    Lane, E.S.; Winter, J.A.

    1982-01-01

    Water is removed from a gel material by contacting the gel material with an organic liquid and contacting the organic liquid with a gas such that water is taken up by the gas. The invention, in one embodiment, may be used to dry gel materials whilst maintaining an open porous network therein. In one example, the invention is applied to gel precipitated spheres containing uranium and plutonium. (author)

  4. Removal of bromates from water

    Barlokova, D.; Ilavsky, J.; Marko, I.; Tkacova, J.

    2017-10-01

    Bromates are substances that are usually not present in drinking water. They are obtained by ozone disinfection in the presence of bromine ions in water, as an impurity of sodium hypochlorite, respectively. Because of their specific properties, bromates are classified as vary dangers substances, that can cause serious illnesses in humans. There are several technological processes that have been used to the removal of bromates from water at present. In this article, the removal of the bromates from water by the adsorption using various sorbent materials (activated carbon, zeolite, Klinopur-Mn, Bayoxide E33, GEH, Read-As and Activated alumina) are presented. The effectiveness of selected sorbent materials in the removal of bromates from drinking water moves in the interval from 10 to 40%. Based on laboratory results, the zeolite can be used to reduce the concentration of bromates in water.

  5. Conserved water molecules in bacterial serine hydroxymethyltransferases.

    Milano, Teresa; Di Salvo, Martino Luigi; Angelaccio, Sebastiana; Pascarella, Stefano

    2015-10-01

    Water molecules occurring in the interior of protein structures often are endowed with key structural and functional roles. We report the results of a systematic analysis of conserved water molecules in bacterial serine hydroxymethyltransferases (SHMTs). SHMTs are an important group of pyridoxal-5'-phosphate-dependent enzymes that catalyze the reversible conversion of l-serine and tetrahydropteroylglutamate to glycine and 5,10-methylenetetrahydropteroylglutamate. The approach utilized in this study relies on two programs, ProACT2 and WatCH. The first software is able to categorize water molecules in a protein crystallographic structure as buried, positioned in clefts or at the surface. The other program finds, in a set of superposed homologous proteins, water molecules that occur approximately in equivalent position in each of the considered structures. These groups of molecules are referred to as 'clusters' and represent structurally conserved water molecules. Several conserved clusters of buried or cleft water molecules were found in the set of 11 bacterial SHMTs we took into account for this work. The majority of these clusters were not described previously. Possible structural and functional roles for the conserved water molecules are envisaged. This work provides a map of the conserved water molecules helpful for deciphering SHMT mechanism and for rational design of molecular engineering experiments. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

  6. GLYPHOSATE REMOVAL FROM DRINKING WATER

    Activated-carbon, oxidation, conventional-treatment, filtration, and membrane studies are conducted to determine which process is best suited to remove the herbicide glyphosate from potable water. Both bench-scale and pilot-scale studies are completed. Computer models are used ...

  7. Removal of ciprofloxacin from water by birnessite

    Jiang, Wei-Teh, E-mail: atwtj@mail.ncku.edu.tw [Department of Earth Sciences, National Cheng Kung University, Tainan 70101, Taiwan (China); Chang, Po-Hsiang; Wang, Ya-Siang; Tsai, Yolin; Jean, Jiin-Shuh [Department of Earth Sciences, National Cheng Kung University, Tainan 70101, Taiwan (China); Li, Zhaohui, E-mail: li@uwp.edu [Department of Earth Sciences, National Cheng Kung University, Tainan 70101, Taiwan (China); Department of Geosciences, University of Wisconsin – Parkside, Kenosha, WI 53144 (United States); Krukowski, Keith [Department of Geosciences, University of Wisconsin – Parkside, Kenosha, WI 53144 (United States)

    2013-04-15

    Highlights: ► Ciprofloxacin removal by birnessite was accompanied by interlayer cation exchange. ► Layer expansion and FTIR data suggested ciprofloxacin intercalation into birnessite. ► Adsorption capacity of ciprofloxacin into birnessite was limited by surface area. ► Birnessite in soil systems may provide host for ciprofloxacin accumulation. -- Abstract: With more pharmaceuticals and personal care products detected in the surface and waste waters, studies on interactions between these contaminants and soils or sediments have attracted great attention. In this study, the removal of ciprofloxacin (CIP), a fluoroquinolone antibiotic, by birnessite, a layered manganese oxide, in aqueous solution was investigated by batch studies supplemented by X-ray diffraction (XRD) and Fourier transform infrared analyses. Stoichiometric release of exchangeable cations accompanying CIP removal from water confirmed cation exchange as the major mechanism for CIP uptake by birnessite. Interlayer expansion after CIP adsorption on birnessite as revealed by XRD analyses indicated that intercalation contributed significantly to CIP uptake in addition to external surface adsorption. Correlation of CIP adsorption to specific surface area and cation exchange capacity suggested that the former was the limiting factor for CIP uptake. At the adsorption maximum, CIP molecules formed a monolayer on the birnessite surfaces. The adsorbed CIP could be partially removed using a cationic surfactant at a low initial concentration and mostly removed by AlCl{sub 3} at a higher initial concentration, which further supported the cation exchange mechanism for CIP removal by birnessite. The results indicated that the presence of layered Mn-oxide in the soil and waste water treatment systems may provide host for CIP accumulation.

  8. Removal of ciprofloxacin from water by birnessite

    Jiang, Wei-Teh; Chang, Po-Hsiang; Wang, Ya-Siang; Tsai, Yolin; Jean, Jiin-Shuh; Li, Zhaohui; Krukowski, Keith

    2013-01-01

    Highlights: ► Ciprofloxacin removal by birnessite was accompanied by interlayer cation exchange. ► Layer expansion and FTIR data suggested ciprofloxacin intercalation into birnessite. ► Adsorption capacity of ciprofloxacin into birnessite was limited by surface area. ► Birnessite in soil systems may provide host for ciprofloxacin accumulation. -- Abstract: With more pharmaceuticals and personal care products detected in the surface and waste waters, studies on interactions between these contaminants and soils or sediments have attracted great attention. In this study, the removal of ciprofloxacin (CIP), a fluoroquinolone antibiotic, by birnessite, a layered manganese oxide, in aqueous solution was investigated by batch studies supplemented by X-ray diffraction (XRD) and Fourier transform infrared analyses. Stoichiometric release of exchangeable cations accompanying CIP removal from water confirmed cation exchange as the major mechanism for CIP uptake by birnessite. Interlayer expansion after CIP adsorption on birnessite as revealed by XRD analyses indicated that intercalation contributed significantly to CIP uptake in addition to external surface adsorption. Correlation of CIP adsorption to specific surface area and cation exchange capacity suggested that the former was the limiting factor for CIP uptake. At the adsorption maximum, CIP molecules formed a monolayer on the birnessite surfaces. The adsorbed CIP could be partially removed using a cationic surfactant at a low initial concentration and mostly removed by AlCl 3 at a higher initial concentration, which further supported the cation exchange mechanism for CIP removal by birnessite. The results indicated that the presence of layered Mn-oxide in the soil and waste water treatment systems may provide host for CIP accumulation

  9. Removal of radium from drinking water

    Lauch, R.P.

    1992-08-01

    The report summarizes processes for removal of radium from drinking water. Ion exchange, including strong acid and weak acid resin, is discussed. Both processes remove better than 95 percent of the radium from the water. Weak acid ion exchange does not add sodium to the water. Calcium cation exchange removes radium and can be used when hardness removal is not necessary. Iron removal processes are discussed in relation to radium removal. Iron oxides remove much less than 20 percent of the radium from water under typical conditions. Manganese dioxide removes radium from water when competition for sorption sites and clogging of sites is reduced. Filter sand that is rinsed daily with dilute acid will remove radium from water. Manganese dioxide coated filter sorption removes radium but more capacity would be desirable. The radium selective complexer selectively removes radium with significant capacity if iron fouling is eliminated

  10. Water Distribution and Removal Model

    Y. Deng; N. Chipman; E.L. Hardin

    2005-01-01

    The design of the Yucca Mountain high level radioactive waste repository depends on the performance of the engineered barrier system (EBS). To support the total system performance assessment (TSPA), the Engineered Barrier System Degradation, Flow, and Transport Process Model Report (EBS PMR) is developed to describe the thermal, mechanical, chemical, hydrological, biological, and radionuclide transport processes within the emplacement drifts, which includes the following major analysis/model reports (AMRs): (1) EBS Water Distribution and Removal (WD and R) Model; (2) EBS Physical and Chemical Environment (P and CE) Model; (3) EBS Radionuclide Transport (EBS RNT) Model; and (4) EBS Multiscale Thermohydrologic (TH) Model. Technical information, including data, analyses, models, software, and supporting documents will be provided to defend the applicability of these models for their intended purpose of evaluating the postclosure performance of the Yucca Mountain repository system. The WD and R model ARM is important to the site recommendation. Water distribution and removal represents one component of the overall EBS. Under some conditions, liquid water will seep into emplacement drifts through fractures in the host rock and move generally downward, potentially contacting waste packages. After waste packages are breached by corrosion, some of this seepage water will contact the waste, dissolve or suspend radionuclides, and ultimately carry radionuclides through the EBS to the near-field host rock. Lateral diversion of liquid water within the drift will occur at the inner drift surface, and more significantly from the operation of engineered structures such as drip shields and the outer surface of waste packages. If most of the seepage flux can be diverted laterally and removed from the drifts before contacting the wastes, the release of radionuclides from the EBS can be controlled, resulting in a proportional reduction in dose release at the accessible environment

  11. Water Distribution and Removal Model

    Y. Deng; N. Chipman; E.L. Hardin

    2005-08-26

    The design of the Yucca Mountain high level radioactive waste repository depends on the performance of the engineered barrier system (EBS). To support the total system performance assessment (TSPA), the Engineered Barrier System Degradation, Flow, and Transport Process Model Report (EBS PMR) is developed to describe the thermal, mechanical, chemical, hydrological, biological, and radionuclide transport processes within the emplacement drifts, which includes the following major analysis/model reports (AMRs): (1) EBS Water Distribution and Removal (WD&R) Model; (2) EBS Physical and Chemical Environment (P&CE) Model; (3) EBS Radionuclide Transport (EBS RNT) Model; and (4) EBS Multiscale Thermohydrologic (TH) Model. Technical information, including data, analyses, models, software, and supporting documents will be provided to defend the applicability of these models for their intended purpose of evaluating the postclosure performance of the Yucca Mountain repository system. The WD&R model ARM is important to the site recommendation. Water distribution and removal represents one component of the overall EBS. Under some conditions, liquid water will seep into emplacement drifts through fractures in the host rock and move generally downward, potentially contacting waste packages. After waste packages are breached by corrosion, some of this seepage water will contact the waste, dissolve or suspend radionuclides, and ultimately carry radionuclides through the EBS to the near-field host rock. Lateral diversion of liquid water within the drift will occur at the inner drift surface, and more significantly from the operation of engineered structures such as drip shields and the outer surface of waste packages. If most of the seepage flux can be diverted laterally and removed from the drifts before contacting the wastes, the release of radionuclides from the EBS can be controlled, resulting in a proportional reduction in dose release at the accessible environment. The purposes

  12. ARSENIC REMOVAL FROM DRINKING WATER BY IRON REMOVAL PLANTS

    This report documents a long term performance study of two iron removal water treatment plants to remove arsenic from drinking water sources. Performance information was collected from one system located in midwest for one full year and at the second system located in the farwest...

  13. Removal of mercury from water using pottery

    Helal, A.A.A.

    2006-01-01

    In a previous study, the sorption of radiocobalt by powdered pottery materials was investigated. The use of these materials as immobilization matrix for liquid radioactive waste requires the employment of pottery vessels. Therefore, the present study aims to give detailed investigations of the decontamination of radionuclides and toxic elements using pottery containers. These investigations are equally useful to elucidate how far these vessels can be utilized for water purification through decontamination of toxic and heavy metals. The radionuclide or heavy metal removal capability using pottery pots, as low cost sorbents, has been investigated for both radioactive ( 203 Hg) and stable mercury. The results indicated that Hg 2+ is better removed by pottery from neutral to alkaline solutions. The capacity of the used pottery container (100 ml in volume) for complete removal of mercury was found to reach 3 x 10 -4 mol/l, and the time needed was 8 hours. The sorption process was suggested to occur via adsorption and ion exchange. The effect of presence of humic or fulvic acid, as ligands abundant in water, is also investigated. The results imply that, in absence of humic or fulvic acid the sorption follows the expected behaviour, i.e. sorption sites with similar affinity for mercury. In presence of humic or fulvic acid, additional sorption sites are available by the organic molecule when it is associated to the pottery. (orig.)

  14. PRTR ion exchange vault water removal

    Ham, J.E.

    1995-11-01

    This report documents the removal of radiologically contaminated water from the Plutonium Recycle Test Reactor (PRTR) ion exchange vault. Approximately 57,000 liters (15,000 gallons) of water had accumulated in the vault due to the absence of a rain cover. The water was removed and the vault inspected for signs of leakage. No evidence of leakage was found. The removal and disposal of the radiologically contaminated water decreased the risk of environmental contamination

  15. THE REMOVAL OF GLYPHOSATE FROM DRINKING WATER

    The effectiveness of granulated activated carbon (GAC), packed activated carbon (PAC), conventional treatment, membranes, and oxidation for removing glyphosate from natural waters is evaluated. Results indicate that GAC and PAC are not effective in removing glyphosate, while oxid...

  16. ADSORPTIVE REMOVAL OF FLUORIDE FROM WATER USING ...

    Preferred Customer

    Currently available treatment methods for removal of excess fluoride from water are broadly divided into three ... the application of nanoparticles as sorbents for fluoride removal. Sundaram [26] studied the ... Characterization of adsorbent.

  17. 49 CFR 193.2173 - Water removal.

    2010-10-01

    ... 49 Transportation 3 2010-10-01 2010-10-01 false Water removal. 193.2173 Section 193.2173...: FEDERAL SAFETY STANDARDS Design Impoundment Design and Capacity § 193.2173 Water removal. (a) Impoundment areas must be constructed such that all areas drain completely to prevent water collection. Drainage...

  18. Water Recycling removal using temperature-sensitive hydronen

    Rana B. Gupta

    2002-10-30

    The overall objective of this project was to study the proposed Water Recycling/Removal Using Temperature-Sensitive Hydrogels. The main element of this technology is the design of a suitable hydrogel that can perform needed water separation for pulp and paper industry. The specific topics studied are to answer following questions: (a) Can water be removed using hydrogel from large molecules such as lignin? (b) Can the rate of separation be made faster? (c) What are the molecular interactions with hydrogel surface? (d) Can a hydrogel be designed for a high ionic strength and high temperature? Summary of the specific results are given.

  19. Removal of radionuclides from household water

    Vesterbacka, P.; Turtiainen, T.; Haemaelaeinen, K.; Salonen, L.; Arvela, H.

    2003-10-01

    Research upon methods for removing radionuclides from household water was initiated in Finland in 1995. Three research projects, of which two were carried out with National Technology Agency of Finland and one with CEC, have been completed by the end of 2002. One of the main objectives of the research was to compose a guidebook for consumers and water treatment companies. Radon can be removed from household water by aeration and by activated carbon filtration. Aerators that are well designed and set up can remove over 90% of waterborne radon. The best aerators have achieved removal efficiencies that are nearly 100%. However, setting up an aeration system requires thorough planning. Also, activated carbon filtration removes radon efficiently. The removal efficiencies have been over 90%, often nearly 100%. Depending on the water quality and usage, the carbon batch inside the filter needs to be changed every 2-3 years. Since activated carbon filters emit gamma radiation while in use, they should not be installed inside the dwelling but in a separate building or by the well. It is recommended that uranium be removed from drinking water by anion exchange, which is the most efficient removal method for this purpose. Typically, the removal efficiencies are nearly 100%. The one exception is the so called tap filter, the removal efficiency of which depends on uranium concentration in raw water and the rate of water flow. High saline concentration in water may extricate uranium from ion exchange resin. Changes in plumbing pressure or pH-value do not have any significant influence in uranium retention. Removal efficiencies of lead and polonium vary a lot depending on the chemical form in which they occur in water. They can be reliably removed from water by reverse osmosis only. Other treatment methods, such as ion exchange and activated carbon filtration, remove lead and polonium partly. Lead and polonium are removed more efficiently when they are bound onto smaller particles

  20. Removal of radionuclides from household water

    Vesterbacka, P.; Turtiainen, T.; Haemaelaeinen, K.; Salonen, L.; Arvela, H.

    2007-02-01

    Research upon methods for removing radionuclides from household water was initiated in Finland in 1995. Three research projects, of which two were carried out with National Technology Agency of Finland and one with CEC, have been completed by the end of 2002. One of the main objectives of the research was to compose a guidebook for consumers and water treatment companies. Radon can be removed from household water by aeration and by activated carbon filtration. Aerators that are well designed and set up can remove over 90% of waterborne radon. The best aerators have achieved removal efficiencies that are nearly 100%. However, setting up an aeration system requires thorough planning. Also, activated carbon filtration removes radon efficiently. The removal efficiencies have been over 90%, often nearly 100%. Depending on the water quality and usage, the carbon batch inside the filter needs to be changed every 2 - 3 years. Since activated carbon filters emit gamma radiation while in use, they should not be installed inside the dwelling but in a separate building or by the well. It is recommended that uranium be removed from drinking water by anion exchange, which is the most efficient removal method for this purpose. Typically, the removal efficiencies are nearly 100%. The one exception is the so called tap filter, the removal efficiency of which depends on uranium concentration in raw water and the rate of water flow. High saline concentration in water may extricate uranium from ion exchange resin. Changes in plumbing pressure or pH-value do not have any significant influence in uranium retention. Removal efficiencies of lead and polonium vary a lot depending on the chemical form in which they occur in water. They can be reliably removed from water by reverse osmosis only. Other treatment methods, such as ion exchange and activated carbon filtration, remove lead and polonium partly. Lead and polonium are removed more efficiently when they are bound onto smaller

  1. Nitrate Removal from Ground Water: A Review

    Archna

    2012-01-01

    Full Text Available Nitrate contamination of ground water resources has increased in Asia, Europe, United States, and various other parts of the world. This trend has raised concern as nitrates cause methemoglobinemia and cancer. Several treatment processes can remove nitrates from water with varying degrees of efficiency, cost, and ease of operation. Available technical data, experience, and economics indicate that biological denitrification is more acceptable for nitrate removal than reverse osmosis and ion exchange. This paper reviews the developments in the field of nitrate removal processes which can be effectively used for denitrifying ground water as well as industrial water.

  2. Iron and manganese removal from drinking water

    Pascu, Daniela-Elena; Neagu (Pascu), Mihaela; Alina Traistaru, Gina; Nechifor, Aurelia Cristina; Raluca Miron, Alexandra

    2016-01-01

    The purpose of the present study is to find a suitable method for removal of iron and manganese from ground water, considering both local economical and environmental aspects. Ground water is a highly important source of drinking water in Romania. Ground water is naturally pure from bacteria at a 25 m depth or more. However, solved metals may occur and if the levels are too high, the water is not drinkable. Different processes, such as electrochemical and combined electrochemical-adsorption m...

  3. Norm removal from frac water

    Silva, James Manio; Matis, Hope; Kostedt, IV, William Leonard

    2014-11-18

    A method for treating low barium frac water includes contacting a frac water stream with a radium selective complexing resin to produce a low radium stream, passing the low radium stream through a thermal brine concentrator to produce a concentrated brine; and passing the concentrated brine through a thermal crystallizer to yield road salt.

  4. Removal of oil from water by bentonite

    Moazed, H.; Viraraghavan, T.

    1999-01-01

    Many materials, included activated carbon, peat, coal, fiberglass, polypropylene, organoclay and bentonite have been used for removing oils and grease from water. However, bentonite has been used only rarely for this purpose. In this study Na-bentonite was used to remove oil from oil-in-water emulsions of various kinds such as standard mineral oil, cutting oils, refinery effluent and produced water from production wells at Estevan, Saskatchewan. Removal efficiencies obtained were 85 to 96 per cent for cutting oils, 84 to 86 per cent for produced water and 54 to 87 per cent for refinery effluent. Bentonite proved to be more effective in the removal of oil from oil-in-water emulsions than from actual waste waters; up to 96 percent from oil-in-water emulsions to only 87 per cent from actual waste water. The percentage of oil removed was found to be a function of the amount of bentonite added and the adsorption time up to the equilibrium time. Result also showed that the Langmuir, Freundlich and BET isotherms are well suited to describe the adsorption of oil by bentonite from the various oily waters employed in this study. 15 refs

  5. N-Basin water removal plan

    Nellesen, A.L.

    1997-07-01

    This ALARA review provides a description of the engineering and administrative controls used to manage personnel exposure, control contamination levels, and airborne radioactivity concentrations, while removing water and stabilizing surfaces in the 105-N Fuel Storage Building

  6. Nitrate Removal from Ground Water: A Review

    Archna; Sharma, Surinder K.; Sobti, Ranbir Chander

    2012-01-01

    Nitrate contamination of ground water resources has increased in Asia, Europe, United States, and various other parts of the world. This trend has raised concern as nitrates cause methemoglobinemia and cancer. Several treatment processes can remove nitrates from water with varying degrees of efficiency, cost, and ease of operation. Available technical data, experience, and economics indicate that biological denitrification is more acceptable for nitrate removal than reverse osmosis and ion ex...

  7. Arsenic removal for ceramic water filters

    Mishant Kumar

    2013-02-01

    Full Text Available Arsenic in drinking water is a hazard to human health and is a known carcinogen (Mass 1992. Resource Development International – Cambodia (RDIC has researched, developed, and manufactured simple ceramic water fi lters (CWF which have proved to be extremely effective in removing pathogens from water. These fi lters however, do not remove arsenic from water, which exists in the source water at levels above the World Health Organisation (WHO guideline of 10μg/L. The aims of this literature based study were to investigate conventional and non-conventional arsenic removal processes, and to discuss the options for applying an arsenic removal technology to the CWFs produced by RDIC. It was found that conventional arsenic removal technologies are diffi cult to implement in the context of household water treatment in a developing country. This study suggested that non-conventional arsenic removal technologies shall be more effective and that field studies must be undertaken to verify the success of such methods.

  8. Boron removal from geothermal waters by electrocoagulation

    Yilmaz, A. Erdem [Atatuerk University, Faculty of Engineering, Department of Environmental Engineering., 25240 Erzurum (Turkey)], E-mail: aerdemy@atauni.edu.tr; Boncukcuoglu, Recep [Atatuerk University, Faculty of Engineering, Department of Environmental Engineering., 25240 Erzurum (Turkey); Kocakerim, M. Muhtar [Atatuerk University, Faculty of Engineering, Department of Chemical Engineering, 25240 Erzurum (Turkey); Yilmaz, M. Tolga; Paluluoglu, Cihan [Atatuerk University, Faculty of Engineering, Department of Environmental Engineering., 25240 Erzurum (Turkey)

    2008-05-01

    Most of the geothermal waters in Turkey contain extremely high concentration of boron when they are used for irrigation. The use of geothermal waters for irrigation can results in excess amount deposition of boron in soil. On the other hand, a minimal boron concentration is required for irrigational waters. In this study, electrocoagulation (EC) was selected as a treatment process for the removal of boron from thermal waters obtained from Ilica-Erzurum in Turkey. Current density (CD), pH of solution and temperature of solution were selected as operational parameters. The results showed that boron removal efficiency increased from pH 4.0 to 8.0 and decreased at pH 10.0. Although boron removal efficiency was highest at pH 8.0, energy consumption was very high at this pH value compared to other pH intervals. Boron removal efficiency reached to 95% with increasing current density from 1.5 to 6.0 mA/cm{sup 2}, but energy consumption was also increased in this interval. At higher temperatures of solution, such as 313 and 333 K, boron removal efficiency increased. At optimum conditions, boron removal efficiency in geothermal water reached up to 95%.

  9. Boron removal from geothermal waters by electrocoagulation

    Yilmaz, A. Erdem; Boncukcuoglu, Recep; Kocakerim, M. Muhtar; Yilmaz, M. Tolga; Paluluoglu, Cihan

    2008-01-01

    Most of the geothermal waters in Turkey contain extremely high concentration of boron when they are used for irrigation. The use of geothermal waters for irrigation can results in excess amount deposition of boron in soil. On the other hand, a minimal boron concentration is required for irrigational waters. In this study, electrocoagulation (EC) was selected as a treatment process for the removal of boron from thermal waters obtained from Ilica-Erzurum in Turkey. Current density (CD), pH of solution and temperature of solution were selected as operational parameters. The results showed that boron removal efficiency increased from pH 4.0 to 8.0 and decreased at pH 10.0. Although boron removal efficiency was highest at pH 8.0, energy consumption was very high at this pH value compared to other pH intervals. Boron removal efficiency reached to 95% with increasing current density from 1.5 to 6.0 mA/cm 2 , but energy consumption was also increased in this interval. At higher temperatures of solution, such as 313 and 333 K, boron removal efficiency increased. At optimum conditions, boron removal efficiency in geothermal water reached up to 95%

  10. Removal of arsenic and iron removal from drinking water using coagulation and biological treatment.

    Pramanik, Biplob Kumar; Pramanik, Sagor Kumar; Suja, Fatihah

    2016-02-01

    Effects of biological activated carbon (BAC), biological aerated filter (BAF), alum coagulation and Moringa oleifera coagulation were investigated to remove iron and arsenic contaminants from drinking water. At an initial dose of 5 mg/L, the removal efficiency for arsenic and iron was 63% and 58% respectively using alum, and 47% and 41% respectively using Moringa oleifera. The removal of both contaminants increased with the increase in coagulant dose and decrease in pH. Biological processes were more effective in removing these contaminants than coagulation. Compared to BAF, BAC gave greater removal of both arsenic and iron, removing 85% and 74%, respectively. Longer contact time for both processes could reduce the greater concentration of arsenic and iron contaminants. The addition of coagulation (at 5 mg/L dosage) and a biological process (with 15 or 60 min contact time) could significantly increase removal efficiency, and the maximum removal was observed for the combination of alum and BAC treatment (60 min contact time), with 100% and 98.56% for arsenic and iron respectively. The reduction efficiency of arsenic and iron reduced with the increase in the concentration of dissolved organics in the feedwater due to the adsorption competition between organic molecules and heavy metals.

  11. Radium removal from Australian spa waters

    Dickson, B.L.; Meakins, R.L.; Bland, C.J.

    1982-01-01

    The dissolved radium content of some mineral spring waters in Victoria and Queensland has been found to exceed the maximum permissible concentration in drinking water. Activities in excess of 40 pCi/1 were measured in some bottles. Studies revealed that the dissolved radium content decreased markedly if the spring water was aerated and filtered prior to bottling. The sediment removed contained ferric hydroxide which is a natural scavenging agent for radium. The formation of such sediments in storage tanks and their removal prior to bottling may create a possible radiation hazard

  12. Uranium speciation and removal from well water

    Ayaz, B.; DeVol, T.; Navratil, J.D.

    2001-01-01

    The purpose of this work was to determine the form of uranium present in the well water and to test the effectiveness of common household treatment devices to remove uranium and radium. Batch tests with activated carbon, iron powder, anion exchange resin and cation exchange resin were used to characterize the form of uranium in the drinking water. In the tests, water and the separation materials were first equilibrated, filtered and then analyzed by alpha spectrometry. The results of the batch tests showed that it is possible to remove greater than 90% of the uranium and radium in the drinking water by using any of the sorbents listed above. Simple filtration with 0.1 μm had little to no impact on uranium removal. Results of tests using household treatment devices will also be presented. (authors)

  13. Autodissociation of a water molecule in liquid water

    Geissler, Phillip L.; Dellago, Christoph; Chandler, David; Hutter, Jurg; Parrinello, Michele

    2000-04-01

    The dissociation of a water molecule in liquid water is the fundamental event in acid-base chemistry, determining the pH of water.Because the microscopic dynamics of this autodissociation are difficult to probe, both by experiment and by computer simulation, its mechanism has been unknown. Here we report several autodissociation trajectories generated by ab initio molecular dynamics [1]. These trajectories, which were harvested using transition path sampling [2-4], reveal the mechanism for the first time. Rare fluctuations in solvation energies destabilize an oxygen-hydrogen bond. Through the transfer of one or more protons along a hydrogen bond.

  14. Slow neutron scattering by water molecules

    Stancic, V [Boris Kidric Institute of Nuclear Sciences Vinca, Beograd (Yugoslavia)

    1970-07-01

    In this work some new, preliminary formulae for slow neutron scattering cross section calculation by heavy and light water molecules have been done. The idea was to find, from the sum which exists in well known Nelkin model, other cross sections in a more simple analytical form, so that next approximations may be possible. In order to sum a series it was starting from Euler-Mclaurin formula. Some new summation formulae have been derived there, and defined in two theorems. Extensive calculations, especially during the evaluation of residues, have been made at the CDC 3600 computer. validation of derived formulae was done by comparison with the BNL-325 results. Good agreement is shown. (author)

  15. Slow neutron scattering by water molecules

    Stancic, V.

    1970-01-01

    In this work some new, preliminary formulae for slow neutron scattering cross section calculation by heavy and light water molecules have been done. The idea was to find, from the sum which exists in well known Nelkin model, other cross sections in a more simple analytical form, so that next approximations may be possible. In order to sum a series it was starting from Euler-Mclaurin formula. Some new summation formulae have been derived there, and defined in two theorems. Extensive calculations, especially during the evaluation of residues, have been made at the CDC 3600 computer. validation of derived formulae was done by comparison with the BNL-325 results. Good agreement is shown. (author)

  16. Uranium removal from the water supply

    Miranzadeh, Mohammad Bagher.

    1996-01-01

    Uranium can be naturally occurring radionuclides that contaminate some potable water supplies. Uranium is found both in surface water and ground water supplies. The United States Environmental Protection Agency recently proposed a maximum contaminant of 20 micro gram/liter for uranium because of concerns about its association with kidney disease and cancer. uranium can be removed from the supply by strong base anion-resin. Exhausted resin is regenerated by sodium chloride solution. (Author)

  17. REMOVAL OF HEXAVALENT CHROMIUM FROM DRINKING WATER

    A. R. Asgari ، F. Vaezi ، S. Nasseri ، O. Dördelmann ، A. H. Mahvi ، E. Dehghani Fard

    2008-10-01

    Full Text Available Removal of chromium can be accomplished by various methods but none of them is cost-effective in meeting drinking water standards. For this study, granular ferric hydroxide was used as adsorbent for removal of hexavalent chromium. Besides, the effects of changing contact time, pH and concentrations of competitive anions were determined for different amounts of granular ferric hydroxide. It was found that granular ferric hydroxide has a high capacity for adsorption of hexavalent chromium from water at pH≤7 and in 90 min contact time. Maximum adsorption capacity was determined to be 0.788 mg Cr+6/g granular ferric hydroxide. Although relatively good adsorption of sulfate and chloride had been specified in this study, the interfering effects of these two anions had not been detected in concentrations of 200 and 400 mg/L. The absorbability of hexavalent chromium by granular ferric hydroxide could be expressed by Freundlich isotherm with R2>0.968. However, the disadvantage was that the iron concentration in water was increased by the granular ferric hydroxide. Nevertheless, granular ferric hydroxide is a promising adsorbent for chromium removal, even in the presence of other interfering compounds, because granular ferric hydroxide treatment can easily be accomplished and removal of excess iron is a simple practice for conventional water treatment plants. Thus, this method could be regarded as a safe and convenient solution to the problem of chromium-polluted water resources.

  18. Iron and manganese removal from drinking water

    Daniela-Elena Pascu

    2016-04-01

    Full Text Available The purpose of the present study is to find a suitable method for removal of iron and manganese from ground water, considering bothlocal economical and environmental aspects. Ground water is a highly important source of drinking water in Romania. Ground water is naturally pure from bacteria at a 25 m depth or more. However, solved metals may occur and if the levels are too high, the water is not drinkable. Different processes, such as electrochemical and combined electrochemical-adsorption methods have been applied to determine metals content in accordance to reports of National Water Agency from Romania (ANAR. Every water source contains dissolved or particulate compounds. The concentrations of these compounds can affect health, productivity, compliance requirements, or serviceability and cannot be economically removed by conventional filtration means. In this study, we made a comparison between the electrochemical and adsorption methods (using membranes. Both methods have been used to evaluate the efficiency of iron and manganese removal at various times and temperatures. We used two membrane types: composite and cellulose, respectively. Different approaches, including lowering the initial current density and increasing the initial pH were applied. Reaction kinetics was achieved using mathematical models: Jura and Temkin.

  19. Removal of radium from drinking water

    Clifford, D.A.

    1990-01-01

    The traditional, proven process for radium removal are sodium ion exchange softening, lime softening, and reverse osmosis. The newer, radium-specific column processes include adsorption onto the Dow RSC and BaSO 4 -impregnated alumina. The most promising new radium-specific treatment process for large-scale use is adsorption onto preformed manganese dioxide followed by multimedia or diatomaceous earth filtration The disposal of radium-contaminated wastewaters and sludges from processes under consideration will be a major factor in process selection. The processes of choice for municipal water supply treatment to remove radium are sodium ion exchange softening, lime softening, manganese dioxide adsorption-filtration, and selective adsorption onto the Dow RSC or BaSO 4 -impregnated alumina. Where the water is brackish, reverse osmosis hyperfiltration should also be considered. The radium removal process of choice for whole-house or point-of-entry treatment is sodium ion exchange softening. For point-of-use radium removal, a standard reverse osmosis system including cartridge filtration, activated carbon adsorption, and reverse osmosis hyperfiltration is recommended. Although no cost estimates have been made, the relative costs from most expensive to least expansive, for radium removal in small community water supplies are reverse osmosis, sodium ion exchange softening, lime soda softening, manganese dioxide adsorption-filtration, and the radium-selective adsorbents. 34 refs., 7 figs., 2 tabs

  20. Removal of target odorous molecules on to activated carbon cloths.

    Le Leuch, L M; Subrenat, A; Le Cloirec, P

    2004-01-01

    Activated carbon materials are adsorbents whose physico-chemical properties are interesting for the treatment of odorous compounds like hydrogen sulfide. Indeed, their structural parameters (pore structure) and surface chemistry (presence of heteroatoms such as oxygen, hydrogen, nitrogen, sulfur, phosphorus) play an important role in H2S removal. The cloth texture of these adsorbents (activated carbon cloths) is particularly adapted for dealing with high flows, often found in the treatment of odor emissions. Thus, this paper first presents the influence of these parameters through adsorption isothermal curves performed on several materials. Secondly, tests in a dynamic system are described. They highlight the low critical thickness of the fabric compared to granular activated carbon.

  1. Acceleration induced water removal from ear canals.

    Kang, Hosung; Averett, Katelee; Jung, Sunghwan

    2017-11-01

    Children and adults commonly experience having water trapped in the ear canals after swimming. To remove the water, individuals will shake their head sideways. Since a child's ear canal has a smaller diameter, it requires more acceleration of the head to remove the trapped water. In this study, we theoretically and experimentally investigated the acceleration required to break the surface meniscus of the water in artificial ear canals and hydrophobic-coated glass tubes. In experiments, ear canal models were 3D-printed from a CT-scanned human head. Also, glass tubes were coated with silane to match the hydrophobicity in ear canals. Then, using a linear stage, we measured the acceleration values required to forcefully eject the water from the artificial ear canals and glass tubes. A theoretical model was developed to predict the critical acceleration at a given tube diameter and water volume by using a modified Rayleigh-Taylor instability. Furthermore, this research can shed light on the potential of long-term brain injury and damage by shaking the head to push the water out of the ear canal. This research was supported by National Science Foundation Grant CBET-1604424.

  2. Method of arsenic removal from water

    Gadgil, Ashok

    2010-10-26

    A method for low-cost arsenic removal from drinking water using chemically prepared bottom ash pre-treated with ferrous sulfate and then sodium hydroxide. Deposits on the surface of particles of bottom ash form of activated iron adsorbent with a high affinity for arsenic. In laboratory tests, a miniscule 5 grams of pre-treated bottom ash was sufficient to remove the arsenic from 2 liters of 2400 ppb (parts per billion) arsenic-laden water to a level below 50 ppb (the present United States Environmental Protection Agency limit). By increasing the amount of pre-treated bottom ash, even lower levels of post-treatment arsenic are expected. It is further expected that this invention supplies a very low-cost solution to arsenic poisoning for large population segments.

  3. Water removal characteristics of parallel serpentine channels

    Jiao, K.; Zhou, B.; Quan, P. [Windsor Univ., ON (Canada). Dept. of Mechanical, Automotive and Materials Engineering

    2005-07-01

    A study was conducted in which the liquid water behaviours in parallel serpentine channels with manifolds on the cathode side of a proton exchange membrane (PEM) fuel cell stack were examined. A 3-dimensional, unsteady two-phase flow model within the commercial computational fluid dynamics software package FLUENT was used. Membrane electrode assemblies (MEA) were placed on different sides in the numerical analysis. Several water management issues were identified for this type of fuel cell stack by examining the flow behaviours of liquid water and airflow velocity fields. It was shown that water in the outflow manifold could be blocked by air streams from the gas flow channels, with water flowing continuously into the outflow manifold. It was also shown that the pressure drop along all the unit cells can never increase or decrease at the same pace. Water which adheres to the end wall of both the inlet and outlet manifolds is difficult to remove. It was suggested that faster water drainage can be achieved by keeping the MEA side of the gas flow channels close to the outlet of the outflow manifold. It was also suggested that the collecting and separating effect at the serpentine gas flow channels could improve the water drainage. 8 refs., 10 figs.

  4. REDUCING ARSENIC LEVELS IN DRINKING WATER DURING IRON REMOVAL PROCESSES

    The presentation provides an overview of iron removal technology for the removal of arsenic from drinking water. The presentation is divided into several topic topics: Arsenic Chemistry, Treatment Selection, Treatment Options, Case Studies and Iron Removal Processes. Each topic i...

  5. Organically modified clay removes oil from water

    Alther, G.R.

    1995-01-01

    When bentonite or other clays and zeolite are modified with quaternary amines, they become organophilic. Such modified bentonites are used to remove mechanically emulsified oil and grease, and other sparingly soluble organics. Types of oil found in water can include fats, lubricants, cutting fluids, heavy hydrocarbons such as tars, grease, crude oil, diesel oils; and light hydrocarbons such as kerosene, jet fuel, and gasoline. If the organoclay is granulated, it is placed into a liquid phase carbon filter vessel to remove FOGs (Free Oil and Grease) and chlorinated hydrocarbons. In this application the clay is mixed with anthrazite to prevent early plugging of the filter by oil or grease droplets. In batch systems a powdered organoclay is employed. Organoclay removes mechanically emulsified oil and grease at 5--7 times the rate of activated carbon, or 50% of its dry weight. Oil and grease and other large sparingly soluble chlorinated hydrocarbons and NOMs (Natural Organic Matter) blind the pores of activated carbon (and ion-exchange resins), reducing its effectiveness significantly. It is therefore economically advantageous for the end user to prepolish the water before it enters carbon vessels. Operating costs can often be reduced by 50% or more

  6. Performance of a biomass adapted to oncological ward wastewater vs. biomass from municipal WWTP on the removal of pharmaceutical molecules.

    Hamon, P; Moulin, P; Ercolei, L; Marrot, B

    2018-01-01

    The performance of a biomass adapted to Oncological Ward Wastewater (OWW) in a membrane bioreactor (MBR) was compared with that of a municipal WWTP, on the removal of pharmaceutical molecules and more specifically on their overall resistance and purifying ability in the presence of pharmaceutical cocktails. Sorption and biotransformation mechanisms on two antineoplastics, one antibiotic and a painkiller were evaluated. Sludge acclimated to OWW allowed for a 34% increase in the removal rate and in the minimum inhibition concentration. The percentage of the amounts of specific pharmaceutical compounds removed by biotransformation or by sorption were measured. These results are positive, as they show that the observed removal of pharmaceutical molecules by biomass acclimated to OWW can mostly be attributed to developed biotransformation, unlike the biomass from the municipal WWTP for which sorption is sometimes the only removal mechanism. The biotransformation kinetic and the solid-water distribution coefficients in this study show good agreement with literature data, even for much higher pharmaceutical concentrations in OWW. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. Can Microalgae Remove Pharmaceutical Contaminants from Water?

    Xiong, Jiu-Qiang; Kurade, Mayur B; Jeon, Byong-Hun

    2018-01-01

    The increase in worldwide water contamination with numerous pharmaceutical contaminants (PCs) has become an emerging environmental concern due to their considerable ecotoxicities and associated health issues. Microalgae-mediated bioremediation of PCs has recently gained scientific attention, as microalgal bioremediation is a solar-power driven, ecologically comprehensive, and sustainable reclamation strategy. In this review, we comprehensively describe the current research on the possible roles and applications of microalgae for removing PCs from aqueous media. We summarize several novel approaches including constructing microbial consortia, acclimation, and cometabolism for enhanced removal of PCs by microalgae, which would improve practical feasibility of these technologies. Some novel concepts for degrading PCs using integrated processes and genetic modifications to realize algal-based bioremediation technologies are also recommended. Copyright © 2017 Elsevier Ltd. All rights reserved.

  8. Organically modified clay removes oil from water

    Alther, G.R.

    1995-01-01

    When bentonite or other clays and zeolites are modified with quaternary amines, they become organophilic. Such modified bentonites are used to remove mechanically emulsified oil and grease, and other sparingly soluble organics. If the organoclay is granulated, it is placed into a liquid phase carbon filter vessel to remove FOG's and chlorinated hydrocarbons. In this application the clay is mixed with anthrazite to prevent early plugging of the filter by oil or grease droplets. In batch systems a powered organoclay is employed. Types of oil found in water can include fats, lubricants, cutting fluids, heavy hydrocarbons such as tars, grease, crude oil, diesel oils; and light hydrocarbons such as kerosene, jet fuel, and gasoline

  9. The Development of Magnetic Molecules for the Selective Removal of Contaminants

    Bushart, S.P.; Bradbury, D.; Elder, G.; Duffield, J.; Pascual, I.; Ratcliffe, N.

    2006-01-01

    'Magnetic molecules' are a new type of decontaminant for removing dilute dissolved contaminants from solution. Magnetic molecules have a specific ion exchange function to selectively react with a particular type of ionic contamination in a liquid solution. The magnetic molecules also have a very small magnetic ferritin core (ferritin is an iron-III mammalian storage protein having about 10 nm diameter), which enables the magnetic molecule to be removed from solution by magnetic filtration. The ion exchange function is attached to the magnetic ferritin core by organic reaction sequences. The ion exchange function selectively bonds to a specific type of contaminant ion. For example, ion exchange functions can selectively target radioactive contaminant ions such as cobalt, cesium and plutonium. The procedure for decontamination is that the appropriate magnetic molecule (which targets the contaminant which it is desired to remove) is added to the solution and the solution is then passed through a magnetic filter. The contaminant binds to the magnetic molecule and is then removed by the magnetic filter. The magnetic molecule/contaminant can then be recovered from the magnetic filter by back-washing. Work has been undertaken towards the development of magnetic molecules for use as radioactive decontaminants for radioactive waste management purposes. Previously we have reported on the functionalization of ferritin with the chelating agent DTPA and have shown that this can be used to bind Ca(II) in solution and separate it from Na(I) ions by the process of equilibrium dialysis. Approximately 100 DTPA molecules could be bound to the surface of the ferritin molecule. Synthetic conditions have been optimised, and which will be reported here, ferritin has been functionalized with approximately 1200 DTPA molecules per mole of ferritin and used successfully to achieve a quantitative separation of Co(II) from Cs(I) ions by equilibrium dialysis. This separation has been carried

  10. Fluoride removal from water by nano filtration

    Bejaoui, Imen; Mnif, Amine; Hamrouni, Bechir

    2009-01-01

    As any oligo element, fluoride is necessary and beneficial for human health to low concentrations, but an excess amount of fluoride ions in drinking water has been known to cause undesirable effects, especially tooth and bones fluoro sis. The maximum acceptable concentration of fluoride in drinking water was fixed by the World Health Organization according to the climate in the range of 1 mg.L -1 to 1,2 mg.L -1 . Many methods have been used to remove fluoride from water such as precipitation, adsorption, electrocoagulation and membrane processes. Technologies using membrane processes are being used in many applications, particularly for brackish water desalination. Nano filtration seems to be the best process for a good selective defluorination of fluorinated waters. The main objective of this work was to investigate the retention of fluoride anions by nano filtration. The first part of this study deals with the characterisation of the NF HL2514TF membrane. The influence of various experimental parameters such as initial fluoride content, feed pressure, permeate flux, ionic strength, type of cation associated to fluoride and pH were studied in the second part. Results show that the retention order for the salts tested was TR(Na 2 SO 4 ) > TR(CaCl 2 ) > TR(NaCl), showing a retention sequence inversely proportional to the salt diffusion coefficients in water. It was also shown that charge effects could not be neglected, and a titration experiments confirmed that the NF membrane carry a surplus of negatively charged groups. Fluoride retention exceeds 60 pour cent, and increases with increasing concentration, where the rejection mechanism is related to the dielectric effects. Speigler-Kedem model was applied to experimental results in the aim to determine phenomenological parametersσand P s respectively, the reflexion coefficient of the membrane and the solute permeability of ions. The convective and diffusive parts of the mass transfer were quantified with

  11. On the Several Molecules and Nanostructures of Water

    Cynthia Kolb Whitney

    2012-01-01

    Full Text Available This paper investigates the water molecule from a variety of viewpoints. Water can involve different isotopes of Hydrogen and Oxygen, it can form differently shaped isomer molecules, and, when frozen, it occupies space differently than most other substances do. The tool for conducting the investigation of all this is called ‘Algebraic Chemistry’. This tool is a quantitative model for predicting the energy budget for all sorts of changes between different ionization states of atoms that are involved in chemical reactions and in changes of physical state. The model is based on consistent patterns seen in empirical data about ionization potentials, together with rational scaling laws that can interpolate and extrapolate for situations where no data are available. The results of the investigation of the water molecule include comments, both positive and negative, about technologies involving heavy water, poly water, Brown’s gas, and cold fusion.

  12. Quantum Behavior of Water Molecules Confined to Nanocavities in Gemstones.

    Gorshunov, Boris P; Zhukova, Elena S; Torgashev, Victor I; Lebedev, Vladimir V; Shakurov, Gil'man S; Kremer, Reinhard K; Pestrjakov, Efim V; Thomas, Victor G; Fursenko, Dimitry A; Dressel, Martin

    2013-06-20

    When water is confined to nanocavities, its quantum mechanical behavior can be revealed by terahertz spectroscopy. We place H2O molecules in the nanopores of a beryl crystal lattice and observe a rich and highly anisotropic set of absorption lines in the terahertz spectral range. Two bands can be identified, which originate from translational and librational motions of the water molecule isolated within the cage; they correspond to the analogous broad bands in liquid water and ice. In the present case of well-defined and highly symmetric nanocavities, the observed fine structure can be explained by macroscopic tunneling of the H2O molecules within a six-fold potential caused by the interaction of the molecule with the cavity walls.

  13. Role of water in the tribochemical removal of bare silicon

    Chen, Cheng; Xiao, Chen [Tribology Research Institute, National Traction Power Laboratory, Southwest Jiaotong University, Chengdu 610031 (China); Wang, Xiaodong [Center of Micro/Nano Science and Technology, Jiangsu University, Zhenjiang 212013 (China); Zhang, Peng; Chen, Lei; Qi, Yaqiong [Tribology Research Institute, National Traction Power Laboratory, Southwest Jiaotong University, Chengdu 610031 (China); Qian, Linmao, E-mail: linmao@swjtu.edu.cn [Tribology Research Institute, National Traction Power Laboratory, Southwest Jiaotong University, Chengdu 610031 (China)

    2016-12-30

    Highlights: • The wear of bare silicon against SiO{sub 2} micro-spherical tip is a tribochemical process with participation of water. • The water amount at Si/SiO{sub 2} interface plays a significant role on the wear of bare silicon. • The role of water relies on the hydroxylation by auto-ionized OH{sup −}, the hydrolysis of H{sub 2}O molecules, and the dissolution of SiO{sub m}H{sub n} in water. - Abstract: Nanowear tests of bare silicon against a SiO{sub 2} microsphere were conducted in air (relative humidity [RH] = 0%–89%) and water using an atomic force microscope. Experimental results revealed that the water played an important role in the tribochemical wear of the bare silicon. A hillock-like wear trace with a height of 0.7 nm was generated on the bare silicon surface in dry air. As the RH increased, the wear depth increased and reached the maximum level in water. Analysis of frictional dissipated energy suggested that the wear of the bare silicon was not dominated by mechanical interactions. High-resolution transmission electron microscopy detection demonstrated that the silicon atoms and crystal lattice underneath the worn area maintained integral perfectly and thus further confirmed the tribochemical wear mechanism of the bare silicon. Finally, the role of water in the tribochemical wear of the bare silicon may be explained by the following three aspects: the hydroxylation by hydroxyl ions auto-ionized in water, the hydrolytic reaction of water molecules, and the dissolution of the tribochemical product SiO{sub m}H{sub n} in liquid water. With increasing RH, a greater water amount would adsorb to the Si/SiO{sub 2} interface and induce a more serious tribochemical wear on the bare silicon surface. The results of this paper may provide further insight into the tribochemical removal mechanism of bare monocrystalline silicon and furnish the wider reaction cognition for chemical mechanical polishing.

  14. New Sorbents for Removing Arsenic From Water

    McConchie, D. M.; Genc-Fuhrman, H.; Clark, M. W.; Caldicott, W.; Davies-McConchie, F. G.

    2004-12-01

    Elevated concentrations of arsenic in the drinking water used in many countries, including some of the poorest developing countries, and recognition that consuming this water can have serious consequences for human health, have led to increased investigations of ways to obtain safe water supplies. Finding new groundwater resources is a possible solution but this is a costly strategy that has no guarantee of success, particularly in areas where water is already a scarce commodity. The alternative is to treat water that is already available, but existing technologies are usually too expensive, too difficult to operate and maintain, or not completely effective when used in less developed countries or remote areas. There is therefore, an urgent need to find a simple and effective but inexpensive sorbent for arsenic that can be used to treat large volumes of water under less than ideal conditions. In this paper we present the results of field and laboratory trials that used a new, highly cost-effective, sorbent to remove arsenic from contaminated water. BauxsolT is the name given to the cocktail of minerals prepared by treating caustic bauxite refinery residues with Mg and Ca to produce a substance with a reaction pH of about 8.5, a high acid neutralizing capacity and an excellent ability to trap trace metals, metalloids and some other ionic species. The trapped ions are tightly bound by processes that include; precipitation of low solubility neoformational minerals, isomorphous substitution, solid-state diffusion, and adsorption; it is also an excellent flocculant. Although ordinary BauxsolT has an excellent ability to bind arsenate, and to a lesser extent arsenite, this ability can be further increased for particular water types by using activated BauxsolT or BauxsolT combined with small amounts of other reagents. Field trials conducted at the Gilt Edge Mine, South Dakota, showed that the addition of BauxsolT to highly sulfidic waste rock reduced the arsenic

  15. [The method to remove nitrite from tap water by tea].

    Lu, M; Chen, L; Xian, H

    1997-03-01

    Drinking water (tap water) is polluted in pipelines by bacteria after long distance transportation. The water contains nitrite (NO2-) which is potentially harmful to human health. The nitrite concentrations range from 0.10 to 2.0 mg/L. Our experiment proved that NO2- could not be removed by boiling, but could be removed by tea. As a natural antioxidant, tea contains several antioxidants, such as ascorbic acid and catechins, which removed NO2- from tap water effectively.

  16. Towards ligand docking including explicit interface water molecules.

    Gordon Lemmon

    Full Text Available Small molecule docking predicts the interaction of a small molecule ligand with a protein at atomic-detail accuracy including position and conformation the ligand but also conformational changes of the protein upon ligand binding. While successful in the majority of cases, docking algorithms including RosettaLigand fail in some cases to predict the correct protein/ligand complex structure. In this study we show that simultaneous docking of explicit interface water molecules greatly improves Rosetta's ability to distinguish correct from incorrect ligand poses. This result holds true for both protein-centric water docking wherein waters are located relative to the protein binding site and ligand-centric water docking wherein waters move with the ligand during docking. Protein-centric docking is used to model 99 HIV-1 protease/protease inhibitor structures. We find protease inhibitor placement improving at a ratio of 9:1 when one critical interface water molecule is included in the docking simulation. Ligand-centric docking is applied to 341 structures from the CSAR benchmark of diverse protein/ligand complexes [1]. Across this diverse dataset we see up to 56% recovery of failed docking studies, when waters are included in the docking simulation.

  17. Ophthalmic ester removal in the agar state giant molecule; Kantenjo kobunshi de futarusan esuteru jokyo

    NONE

    1999-10-01

    Matsubara professors of Tokyo College of Pharmacy developed the technique which simply removed phthalic ester from the solution. The property in which the giant molecule called the poly N isopropyl acrylamide cohered like the agar, when 32 degrees C is exceeded, was utilized, and the phthalic ester of poor solubility is taken in the flocculation stage. It is expected with that it can be utilized for wastewater treatment and solicitation quantity thing analysis in the environment. (translated by NEDO)

  18. Transport behavior of water molecules through two-dimensional nanopores

    Zhu, Chongqin; Li, Hui; Meng, Sheng

    2014-01-01

    Water transport through a two-dimensional nanoporous membrane has attracted increasing attention in recent years thanks to great demands in water purification and desalination applications. However, few studies have been reported on the microscopic mechanisms of water transport through structured nanopores, especially at the atomistic scale. Here we investigate the microstructure of water flow through two-dimensional model graphene membrane containing a variety of nanopores of different size by using molecular dynamics simulations. Our results clearly indicate that the continuum flow transits to discrete molecular flow patterns with decreasing pore sizes. While for pores with a diameter ≥15 Å water flux exhibits a linear dependence on the pore area, a nonlinear relationship between water flux and pore area has been identified for smaller pores. We attribute this deviation from linear behavior to the presence of discrete water flow, which is strongly influenced by the water-membrane interaction and hydrogen bonding between water molecules

  19. Structures of water molecules in carbon nanotubes under electric fields

    Winarto,; Takaiwa, Daisuke; Yamamoto, Eiji; Yasuoka, Kenji

    2015-01-01

    Carbon nanotubes (CNTs) are promising for water transport through membranes and for use as nano-pumps. The development of CNT-based nanofluidic devices, however, requires a better understanding of the properties of water molecules in CNTs because they can be very different from those in the bulk. Using all-atom molecular dynamics simulations, we investigate the effect of axial electric fields on the structure of water molecules in CNTs having diameters ranging from (7,7) to (10,10). The water dipole moments were aligned parallel to the electric field, which increases the density of water inside the CNTs and forms ordered ice-like structures. The electric field induces the transition from liquid to ice nanotubes in a wide range of CNT diameters. Moreover, we found an increase in the lifetime of hydrogen bonds for water structures in the CNTs. Fast librational motion breaks some hydrogen bonds, but the molecular pairs do not separate and the hydrogen bonds reform. Thus, hydrogen bonds maintain the water structure in the CNTs, and the water molecules move collectively, decreasing the axial diffusion coefficient and permeation rate

  20. The role of water molecules in computational drug design.

    de Beer, Stephanie B A; Vermeulen, Nico P E; Oostenbrink, Chris

    2010-01-01

    Although water molecules are small and only consist of two different atom types, they play various roles in cellular systems. This review discusses their influence on the binding process between biomacromolecular targets and small molecule ligands and how this influence can be modeled in computational drug design approaches. Both the structure and the thermodynamics of active site waters will be discussed as these influence the binding process significantly. Structurally conserved waters cannot always be determined experimentally and if observed, it is not clear if they will be replaced upon ligand binding, even if sufficient space is available. Methods to predict the presence of water in protein-ligand complexes will be reviewed. Subsequently, we will discuss methods to include water in computational drug research. Either as an additional factor in automated docking experiments, or explicitly in detailed molecular dynamics simulations, the effect of water on the quality of the simulations is significant, but not easily predicted. The most detailed calculations involve estimates of the free energy contribution of water molecules to protein-ligand complexes. These calculations are computationally demanding, but give insight in the versatility and importance of water in ligand binding.

  1. Treatment techniques for the removal of radioactive contaminants from drinking water

    Logsdon, Gary S.

    1978-01-01

    Maximum contaminant levels have been set for radioactive contaminants, as required by the Safe Drinking Water Act (PL 93-523). Treatment techniques are available for removing radium and beta-gamma emitters. Presently-used methods of removing radium-226 are precipitative lime softening (80-90% removal) ion exchange softening (95% removal) and reverse osmosis (95% removal). The 5 p Ci/l limit for radium can be met with conventional technology for raw waters in the 5-100 p Ci/l concentration range. Treatment for removal of beta or gamma emitters must be based upon chemical rather than radioactive characteristics of the contaminant. Reverse osmosis can remove a broad spectrum of ions and molecules from water, so it is the process most likely to be used. The maximum contaminant level for beta and gamma radioactivity is an annual dose equivalent to the total body or any organ not to exceed 4 m rem/year. The fate of radionuclides after removal from drinking water should be considered. Presently radium is disposed with other process wastes at softening plants removing radium. Confinement and disposal as a radioactive waste would be very expensive. (author)

  2. REMOVAL OF ARSENIC FROM DRINKING WATER SUPPLIES BY IRON REMOVAL PROCESS

    This design manual is an in-depth presentation of the steps required to design and operate a water treatment plant for removal of arsenic in the As (V) form from drinking water using an iron removal process. The manual also discusses the capital and operating costs including many...

  3. Methods of removing uranium from drinking water. 1. A literature survey. 2. Present municipal water treatment and potential removal methods

    Drury, J.S.; Michelson, D.; Ensminger, J.T.; Lee, S.Y.; White, S.K.

    1982-12-01

    Literature was searched for methods of removing uranium from drinking water. U.S. manufacturers and users of water-treatment equipment and products were also contacted regarding methods of removing uranium from potable water. Based on the results of these surveys, it was recommended that untreated, partially treated, and finished water samples from municipal water-treatment facilities be analyzed to determine the extent of removal of uranium by presently used procedures, and that additional laboratory studies be performed to determine what changes are needed to maximize the effectiveness of treatments that are already in use in existing water-treatment plants

  4. Arsenic removal in drinking water by reverse osmosis

    Ahmad, Md. Fayej

    2012-01-01

    Arsenic is widely distributed in nature in the air, water and soil. Acute and chronic arsenic exposure by drinking water has been reported in many countries, especially Argentina, Bangladesh, India, Mexico, Mongolia, Thailand and Taiwan. There are many techniques used to remove arsenic from drinking water. Among them reverse osmosis is widely used. Therefore the purpose of this study is to find the conditions favorable for removal of arsenic from drinking water by using reverse osmosis ...

  5. Virus removal efficiency of Cambodian ceramic pot water purifiers.

    Salsali, Hamidreza; McBean, Edward; Brunsting, Joseph

    2011-06-01

    Virus removal efficiency is described for three types of silver-impregnated, ceramic water filters (CWFs) produced in Cambodia. The tests were completed using freshly scrubbed filters and de-ionized (DI) water as an evaluation of the removal efficiency of the virus in isolation with no other interacting water quality variables. Removal efficiencies between 0.21 and 0.45 log are evidenced, which is significantly lower than results obtained in testing of similar filters by other investigators utilizing surface or rain water and a less frequent cleaning regime. Other experiments generally found virus removal efficiencies greater than 1.0 log. This difference may be because of the association of viruses with suspended solids, and subsequent removal of these solids during filtration. Variability in virus removal efficiencies between pots of the same manufacturer, and observed flow rates outside the manufacturer's specifications, suggest tighter quality control and consistency may be needed during production.

  6. Turbidity and microbes removal from water using an electrochemical filter

    Venkateswaran, G.; Gokhale, B.K.; Belapurkar, A.D.; Kumbhar, A.G.; Balaji, V.

    2004-01-01

    An in-house designed and fabricated Electrochemical fibrous graphite filter (ECF) was used to remove turbidity and microbes. The filter was found to be effective in removing sub micron size indium turbidity from RAPS-1 moderator water, iron turbidity from Active Process Cooling Water (APCW) of Kaiga Generating Station and microbial reduction from process cooling water RAPS-2. Unlike conventional turbidity removal by addition of coagulants and biocide chemical additions for purification, ECF is a clean way to remove the turbidity without contaminating the system and is best suited for close loop systems

  7. Water removal from a dry barrier cover system

    Stormont, J.C.; Ankeny, M.D.; Tansey, M.K.

    1994-01-01

    The results of the numerical simulations reveal that horizontal air flow through the coarse with reasonable pressure gradients can remove large quantities of water from the cover system. Initially, the water removal from the cover system is dominated by the evaporation and advection of water vapor out of the coarse layer. Once the coarse layer is dry, removal of water by evaporation near the fine/coarse layer interface reduces the local water content and water potential, and water moves toward the fine-coarse layer interface and becomes available for evaporation. This result is important in that it suggests the fine layer water content may be moderated by air flow in the coarse layer. Incorporating diffusion of water vapor from the fine layer into the coarse layer substantially increases the water movement out of the fine layer

  8. Removal of trace metal contaminants from potable water by electrocoagulation

    Heffron, Joe; Marhefke, Matt; Mayer, Brooke K.

    2016-01-01

    This study investigated the effects of four operational and environmental variables on the removal of trace metal contaminants from drinking water by electrocoagulation (EC). Removal efficiencies for five metals (arsenic, cadmium, chromium, lead and nickel) were compared under varying combinations of electrode material, post-treatment, water composition and pH. Iron electrodes out-performed aluminum electrodes in removing chromium and arsenic. At pH 6.5, aluminum electrodes were slightly more...

  9. Water-assisted dehalogenation of thionyl chloride in the presence of water molecules.

    Yeung, Chi Shun; Ng, Ping Leung; Guan, Xiangguo; Phillips, David Lee

    2010-04-01

    A second-order Møller-Plesset perturbation theory (MP2) and density functional theory (DFT) investigation of the dehalogenation reactions of thionyl chloride is reported, in which water molecules (up to seven) were explicitly involved in the reaction complex. The dehalogenation processes of thionyl chloride were found to be dramatically catalyzed by water molecules. The reaction rate became significantly faster as more water molecules became involved in the reaction complex. The dehalogenation processes can be reasonably simulated by the gas-phase water cluster models, which reveals that water molecules can help to solvate the thionyl chloride molecules and activate the release of the Cl(-) leaving group. The computed activation energies were used to compare the calculations to available experimental data.

  10. Removal of trace metal contaminants from potable water by electrocoagulation

    Heffron, Joe; Marhefke, Matt; Mayer, Brooke K.

    2016-06-01

    This study investigated the effects of four operational and environmental variables on the removal of trace metal contaminants from drinking water by electrocoagulation (EC). Removal efficiencies for five metals (arsenic, cadmium, chromium, lead and nickel) were compared under varying combinations of electrode material, post-treatment, water composition and pH. Iron electrodes out-performed aluminum electrodes in removing chromium and arsenic. At pH 6.5, aluminum electrodes were slightly more effective at removing nickel and cadmium, while at pH 8.5, iron electrodes were more effective for these metals. Regardless of electrode, cadmium and nickel removal efficiencies were higher at pH 8.5 than at pH 6.5. Post-EC treatment using membrane filtration (0.45 μm) enhanced contaminant removal for all metals but nickel. With the exception of lead, all metals exhibited poorer removal efficiencies as the ionic strength of the background electrolyte increased, particularly in the very high-solids synthetic groundwaters. Residual aluminum concentrations were lowest at pH 6.5, while iron residuals were lowest in low ionic strength waters. Both aluminum and iron residuals required post-treatment filtration to meet drinking water standards. EC with post-treatment filtration appears to effectively remove trace metal contaminants to potable water standards, but both reactor and source water parameters critically impact removal efficiency.

  11. Vibrational properties of water molecules adsorbed in different zeolitic frameworks

    Crupi, V; Longo, F; Majolino, D; Venuti, V

    2006-01-01

    The perturbation of water 'sorbed' in samples of zeolites of different structural type, genesis, and cation composition (K-, Na-, Mg- and Ca-rich zeolites), namely the CHA framework of a synthetic K-chabazite, the LTA framework of synthetic Na-A and Mg50-A zeolites, and the NAT framework of a natural scolecite, has been studied by FTIR-ATR spectroscopy, in the -10 to +80 o C temperature range. The aim was to show how differences in the chemical composition and/or in the topology of the zeolite framework and, in particular, the possibility for the guest water molecules to develop guest-guest and/or host-guest interactions, lead to substantial differences in their vibrational dynamical properties. The spectra, collected in the O-H stretching and H 2 O bending mode regions, are complex, with multiple bands being observed. As far as water in the CHA and LTA frameworks is concerned, whose behaviour is governed by the balance of water-water, water-framework and water-extra-framework cations interactions, the assignment of the resolved components of the O-H stretching band has been discussed by fitting the band shapes into individual components attributed to H 2 O molecules engaged in different degrees of hydrogen bonding. A detailed quantitative picture of the connectivity pattern of water, as a function of temperature and according to the chemical and topological properties of the environment, is furnished. The H 2 O bending vibrational bands give additional information that perfectly agrees with the results obtained from the analysis of the O-H stretching spectral region. In the case of scolecite, a small-pored zeolite where water-water interactions are eliminated, the increased complexity observed in the infrared spectra in the O-H stretching and H 2 O bending regions was explained as due to the hydrogen bonding between the water molecules and the network, and also with the extra-framework cation. Furthermore, these observations have been correlated with the different

  12. The effectiveness of conventional water treatment in removing ...

    Algal blooms are a global problem due to various negative effects that can compromise water quality, such as the production of metabolites that are responsible for odour, colour, taste and toxins. In drinking water supplies algae can reduce the aesthetics of potable water when not readily removed by conventional water ...

  13. Analysis of microplastics and their removal from water

    Oladejo, Abiola

    2017-01-01

    Removal of microplastics from water was studied using extraction with oil. The aim of the thesis was to remove microplastics from water using an organic medium, and to analyse the amount of microplastics in the media involved. The separation of different microplastic types was done by conducting experiments in the laboratory. The microplastics were made by grinding and sieving plastics with a grinding machine before adding them to water and oil, which serves as the organic medium. Tw...

  14. TURBIDITY REMOVAL FROM SURFACE WATER USING ...

    User

    2016-06-01

    Jun 1, 2016 ... Plant-based coagulants are potential alternatives to chemical coagulants used in drinking water treatment. ... Conventional water treatment systems involve the use of synthetic ..... Thesis, Royal Institute of Technology (KTH),.

  15. Photoionization of water molecules by high energy photons

    Lara Martini

    2017-07-01

    Full Text Available We theoretically study the photoionization of water molecules by high energy photon impact. We develop a model in which the final state wavefunction is given by a Coulomb continuum wavefunction with effective charges and the water molecule bound states are represented using the Moccia's monocentric wavefunctions. We obtain analytical expressions for the transition matrix element that enable the computation of cross sections by numerical quadratures. We compare our predictions for photon energies between 20 and 300 eV with more elaborated theoretical results and experiments. We obtain a very good agreement with experiments, in particular, at enough high energies where there is a lack of elaborated results due to their high computational cost. Received: 15 March 2017, Accepted: 25 June 2017; Edited by: S. Kais; DOI: http://dx.doi.org/10.4279/PIP.090006 Cite as: L Martini, D I R Boll, O A Fojón, Papers in Physics 9, 090006 (2017

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

    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...

  17. TESTING OF CARBONACEOUS ADSORBENTS FOR REMOVAL OF POLLUTANTS FROM WATER

    RAISA NASTAS

    2012-03-01

    Full Text Available Testing of carbonaceous adsorbents for removal of pollutants from water. Relevant direction for improving of quality of potable water is application of active carbons at various stages of water treatments. This work includes complex research dealing with testing of a broad spectrum of carbonaceous adsorbents for removal of hydrogen sulfide and nitrite ions from water. The role of the surface functional groups of carbonaceous adsorbents, their acid-basic properties, and the influence of the type of impregnated heteroatom (N, O, or metals (Fe, Cu, Ni, on removal of hydrogen sulfide species and nitrite ions have been researched. The efficiency of the catalyst obtained from peach stones by impregnation with Cu2+ ions of oxidized active carbon was established, being recommended for practical purposes to remove the hydrogen sulfide species from the sulfurous ground waters. Comparative analysis of carbonaceous adsorbents reveals the importance of surface chemistry for oxidation of nitrite ions.

  18. Present municipal water treatment and potential removal methods

    Lee, S.Y.; White, S.K.; Bondietti, E.A.

    1982-01-01

    Uranium analyses of raw water, intermediate stage, and treated water samples from 20 municipal water treatment plants indicated that the present treatment practices were not effective in removing uranium from raw waters when the influent concentration was in the range of 0.1 to 16 μg/L uranium. Laboratory batch tests revealed that the water softening and coagulant chemicals commonly used were able to remove more than 90% of the dissolved uranium ( < 100 μg/L) in waters if an optimum pH and dosage were provided. Absorbents, titanium oxide and activated charcoal, were also effective in uranium removal under specific conditions. Strong base anion exchange resin was the most efficient uranium adsorbent, and an anion exchange column is a recommended option for the treatment of private well waters containing uranium at higher than desirable levels

  19. Scattering of thermal neutron by the water molecule

    Rosa, L.P.

    The calculation of the differenctial cross section for scattering of thermal neutrons by water, taking into account the translational, rotational and vibrational motions of the water molecule, is presented according to Nelkin' model. Some modifications are presented which have been introduced in the original method to improve the results and an application has been made to reactor physics, by calculating the thermal neutron flux in a homogenous medium containing water and absorver. Thirty thermal energy groups have been used to compute the spectra. Within the limits of error, better agreement has been obtained between theory and experiments by using a modified Nelkin kernel consisting of substituting the asymptotic formulae for the rotational and vibrational motions by more exact expressions, similar to the Buttler model for heavy water

  20. Factors affecting radon removal from Rn-222 enriched water

    Abulfaraj, W.H.; Mamoon, A.

    1994-01-01

    Continued use of potable well water that has elevated levels of Rn-222 is harmful to human health. activated carbon, aeration and heating can remove radon from treated water. Water artificially enriched with Rn-222 using a pitchblende source was studied in a laboratory scale model under controlled conditions. (author), 3 figs., 3 refs

  1. STICKING OF MOLECULES ON NONPOROUS AMORPHOUS WATER ICE

    He, Jiao; Vidali, Gianfranco [Physics Department, Syracuse University, Syracuse, NY 13244 (United States); Acharyya, Kinsuk, E-mail: gvidali@syr.edu [Department of Chemistry, University of Virginia, Charlottesville, VA 22904 (United States)

    2016-05-20

    Accurate modeling of physical and chemical processes in the interstellar medium (ISM) requires detailed knowledge of how atoms and molecules adsorb on dust grains. However, the sticking coefficient, a number between 0 and 1 that measures the first step in the interaction of a particle with a surface, is usually assumed in simulations of ISM environments to be either 0.5 or 1. Here we report on the determination of the sticking coefficient of H{sub 2}, D{sub 2}, N{sub 2}, O{sub 2}, CO, CH{sub 4}, and CO{sub 2} on nonporous amorphous solid water. The sticking coefficient was measured over a wide range of surface temperatures using a highly collimated molecular beam. We showed that the standard way of measuring the sticking coefficient—the King–Wells method—leads to the underestimation of trapping events in which there is incomplete energy accommodation of the molecule on the surface. Surface scattering experiments with the use of a pulsed molecular beam are used instead to measure the sticking coefficient. Based on the values of the measured sticking coefficient, we suggest a useful general formula of the sticking coefficient as a function of grain temperature and molecule-surface binding energy. We use this formula in a simulation of ISM gas–grain chemistry to find the effect of sticking on the abundance of key molecules both on grains and in the gas phase.

  2. The spontaneous synchronized dance of pairs of water molecules

    Roncaratti, Luiz F.; Cappelletti, David; Pirani, Fernando

    2014-01-01

    Molecular beam scattering experiments have been performed to study the effect of long-range anisotropic forces on the collision dynamics of two small polar molecules. The main focus of this paper is on water, but also ammonia and hydrogen sulphide molecules have been investigated, and some results will be anticipated. The intermolecular distances mainly probed are of the order of 1 nm and therefore much larger than the molecular dimensions. In particular, we have found that the natural electric field gradient, generated by different spatial orientations of the permanent electric dipoles, is able to promote the transformation of free rotations into coupled pendular states, letting the molecular partners involved in the collision complex swinging to and fro around the field direction. This long-ranged concerted motion manifested itself as large increases of the magnitude of the total integral cross section. The experimental findings and the theoretical treatment developed to shed light on the details of the process suggest that the transformation from free rotations to pendular states depends on the rotational level of both molecules, on the impact parameter, on the relative collision velocity, on the dipole moment product and occurs in the time scale of picoseconds. The consequences of this intriguing phenomenon may be important for the interpretation and, in perspective, for the control of elementary chemical and biological processes, given by polar molecules, ions, and free radicals, occurring in several environments under various conditions

  3. The spontaneous synchronized dance of pairs of water molecules

    Roncaratti, Luiz F. [Dipartimento di Chimica, Biologia e Biotecnologie, Università degli Studi di Perugia, 06123 Perugia (Italy); Instituto de Física, Universidade de Brasília, 70910-900 Brasília (Brazil); Cappelletti, David, E-mail: david.cappelletti@unipg.it; Pirani, Fernando [Dipartimento di Chimica, Biologia e Biotecnologie, Università degli Studi di Perugia, 06123 Perugia (Italy)

    2014-03-28

    Molecular beam scattering experiments have been performed to study the effect of long-range anisotropic forces on the collision dynamics of two small polar molecules. The main focus of this paper is on water, but also ammonia and hydrogen sulphide molecules have been investigated, and some results will be anticipated. The intermolecular distances mainly probed are of the order of 1 nm and therefore much larger than the molecular dimensions. In particular, we have found that the natural electric field gradient, generated by different spatial orientations of the permanent electric dipoles, is able to promote the transformation of free rotations into coupled pendular states, letting the molecular partners involved in the collision complex swinging to and fro around the field direction. This long-ranged concerted motion manifested itself as large increases of the magnitude of the total integral cross section. The experimental findings and the theoretical treatment developed to shed light on the details of the process suggest that the transformation from free rotations to pendular states depends on the rotational level of both molecules, on the impact parameter, on the relative collision velocity, on the dipole moment product and occurs in the time scale of picoseconds. The consequences of this intriguing phenomenon may be important for the interpretation and, in perspective, for the control of elementary chemical and biological processes, given by polar molecules, ions, and free radicals, occurring in several environments under various conditions.

  4. Treatment technology for removing radon from small community water supplies

    Kinner, N.E.; Quern, P.A.; Schell, G.S.; Lessard, C.E.; Clement, J.A.

    1989-01-01

    Radon contamination of drinking water primarily affects individual homeowners and small communities using ground-water supplies. Presently, three types of treatment processes have been used to remove radon: granular activated carbon adsorption (GAC), diffused-bubble aeration, and packed-tower aeration. In order to obtain data on these treatment alternatives for small communities water supplies, a field evaluation study was conducted on these three processes as well as on several modifications to aeration of water in storage tanks considered to be low cost/low technology alternatives. The paper presents the results of these field studies conducted at a small mobile home park in rural New Hampshire. The conclusion of the study was that the selection of the appropriate treatment system to remove radon from drinking water depends primarily upon: (1) precent removal of process; (2) capital operating and maintenance costs; (3) safety (radiation); and (4) raw water quality (Fe, Mn, bacteria and organics)

  5. Trace-level mercury removal from surface water

    Klasson, K.T.; Bostick, D.T.

    1998-01-01

    Many sorbents have been developed for the removal of mercury and heavy metals from waters; however, most of the data published thus far do not address the removal of mercury to the target levels represented in this project. The application to which these sorbents are targeted for use is the removal of mercury from microgram-per-liter levels to low nanogram-per-liter levels. Sorbents with thiouronium, thiol, amine, sulfur, and proprietary functional groups were selected for these studies. Mercury was successfully removed from surface water via adsorption onto Ionac SR-4 and Mersorb resins to levels below the target goal of 12 ng/L in batch studies. A thiol-based resin performed the best, indicating that over 200,000 volumes of water could be treated with one volume of resin. The cost of the resin is approximately $0.24 per 1,000 gal of water

  6. Removal method of radium in mine water by filter sand

    Taki, Tomihiro; Naganuma, Masaki

    2003-01-01

    Trace radium is contained in mine water from the old mine road in Ningyo-Toge Environmental Engineering Center, JNC. We observed that filter sand with hydrated manganese oxide adsorbed radium in the mine water safely for long time. The removal method of radium by filter sand cladding with hydrated manganese oxide was studied. The results showed that radium was removed continuously and last for a long time from mine water with sodium hypochlorite solution by passing through the filter sand cladding with hydrated manganese. Only sodium hypochlorite solution was used. When excess of it was added, residue chlorine was used as chlorine disinfection. Filter sand cladding with hydrated manganese on the market can remove radium in the mine water. The removal efficiency of radium is the same as the radium coprecipitation method added with barium chloride. The cost is much lower than the ordinary methods. Amount of waste decreased to about 1/20 of the coprecipitation method. (S.Y.)

  7. performance of water filters towards the removal of selected

    Morohani Merinyo

    sand, ceramic and membrane purifier respectively, while, fluoride removal was found to be 95.5% ... associated diseases in developing countries ... The main drinking water risks in developing ... Tanzania Demographic and Health Survey.

  8. Quantification of the Intracellular Life Time of Water Molecules to Measure Transport Rates of Human Aquaglyceroporins.

    Palmgren, Madelene; Hernebring, Malin; Eriksson, Stefanie; Elbing, Karin; Geijer, Cecilia; Lasič, Samo; Dahl, Peter; Hansen, Jesper S; Topgaard, Daniel; Lindkvist-Petersson, Karin

    2017-12-01

    Orthodox aquaporins are transmembrane channel proteins that facilitate rapid diffusion of water, while aquaglyceroporins facilitate the diffusion of small uncharged molecules such as glycerol and arsenic trioxide. Aquaglyceroporins play important roles in human physiology, in particular for glycerol metabolism and arsenic detoxification. We have developed a unique system applying the strain of the yeast Pichia pastoris, where the endogenous aquaporins/aquaglyceroporins have been removed and human aquaglyceroporins AQP3, AQP7, and AQP9 are recombinantly expressed enabling comparative permeability measurements between the expressed proteins. Using a newly established Nuclear Magnetic Resonance approach based on measurement of the intracellular life time of water, we propose that human aquaglyceroporins are poor facilitators of water and that the water transport efficiency is similar to that of passive diffusion across native cell membranes. This is distinctly different from glycerol and arsenic trioxide, where high glycerol transport efficiency was recorded.

  9. Compositions and methods for removing arsenic in water

    Gadgil, Ashok Jagannth [El Cerrito, CA

    2011-02-22

    Compositions and methods and for contaminants from water are provided. The compositions comprise ferric hydroxide and ferric oxyhydride coated substrates for use in removing the contaminant from the water. Contacting water bearing the contaminant with the substrates can substantially reduce contaminant levels therein. Methods of oxidizing the contaminants in water to facilitate their removal by the ferric hydroxide and ferric oxyhydride coated substrates are also provided. The contaminants include, but are not limited to, arsenic, selenium, uranium, lead, cadmium, nickel, copper, zinc, chromium and vanadium, their oxides and soluble salts thereof.

  10. Removal of Strontium from Drinking Water by Conventional ...

    The United States Environmental Protection Agency Contaminant Candidate List 3 lists strontium as a contaminant for potential regulatory consideration in drinking water. There is very little data available on strontium removal from drinking water. As a result, there is an immediate need to perform treatment studies. The objective of this work is to evaluate the effectiveness of conventional and lime-soda ash softening treatments to remove strontium from surface and ground waters. Conventional drinking water treatment with aluminum and iron coagulants were able to achieve 12% and 5.9% strontium removal at best, while lime softening removed as much as 78% from natural strontium-containing ground water. Systematic fundamental experiments showed that strontium removal during the lime-soda ash softening was related to pH, calcium concentration and dissolved inorganic carbon concentration. Final strontium concentration was also directly associated with initial strontium concentration. Precipitated solids showed well-formed crystals or agglomerates of mixed solids, two polymorphs of calcium carbonate (vaterite and calcite), and strontianite, depending on initial water quality conditions. X-ray diffraction analysis suggested that strontium likely replaced calcium inside the crystal lattice and was likely mainly responsible for removal during lime softening. To inform the public.

  11. Removal of soluble toxic metals from water

    Buckley, L.P.; Vijayan, S.; McConeghy, G.J.; Maves, S.R.; Martin, J.F.

    1990-05-01

    The removal of selected, soluble toxic metals from aqueous solutions has been accomplished using a combination of chemical treatment and ultrafiltration. The process has been evaluated at the bench-scale and is undergoing pilot-scale testing. Removal efficiencies in excess of 95-99% have been realized. The test program at the bench-scale investigated the limitations and established the optimum range of operating parameters for the process, while the tests conducted with the pilot-scale process equipment are providing information on longer-term process efficiencies, effective processing rates, and fouling potential of the membranes. With the typically found average concentrations of the toxic metals in groundwaters at Superfund sites used as the feed solution, the process has decreased levels up to 100-fold or more. Experiments were also conducted with concentrated solutions to determine their release from silica-based matrices. The solidified wastes were subjected to EP Toxicity test procedures and met the criteria successfully. The final phase of the program involving a field demonstration at a uranium tailings site will be outlined

  12. Study on arsenic removal process from water

    B Bayarmaa

    2014-09-01

    Full Text Available In this study a novel adsorbent, iron oxide, is used for As (V or As (III removal. Some ferric oxides have been reported to be effective for arsenic removal. Ferric oxides powder is a good adsorbent material since it’s has magnetic properties and a good adsorption capacity. The main purpose of this study has been focused on to study the relationship between adsorption capacity (ability, performance and the surface characteristics of the ferric oxide. Prepared sample’s capacity was evaluated. The value was 26.1-67.4 mg/g for As (V and 20.5-47.8 mg/g for As (III. pH dependence was evaluated and when pH increasing, adsorption capacity was decreased. The kinetic was evaluated and about 12 hours reached equilibrium and a capacity of 49 mg/g for As (V and 42 mg/g for As(III was gained. The kinetic constants for arsenic adsorption on the ferrihydrite adsorbent’s were fitted.DOI: http://dx.doi.org/10.5564/mjc.v12i0.172 Mongolian Journal of Chemistry Vol.12 2011: 53-55

  13. Materials removal by water jets with high relative velocity

    Schikorr, W.

    1986-01-01

    By way of introduction approaches to the systematic apprehension of the material removal by water jets up to 1000 bar are made. In drilling experiments the effects of jet dynamic are studied, using the controlled disintegration of the jet. Using model-layer-systems the removal of layers by the 'natural' disintegrating fluid-jet is examined. The mechanisms of material removal and the consequences on the praxis of cleaning are discussed. A concept to measure specially the effects of the dynamic jet components is developed. In conclusion aspects of progress in this methods of material removal are discussed. (orig.) [de

  14. Removal of some radionuclides from water by bioaccumulation

    Miskovic, D.; Conkic, L.; Dalmacija, B.; Gantar, M.

    1992-01-01

    First objective of this study was to investigate the application of biologically activated carbon (BAC) as well as its comparison to adsorption, with the aim of removing some radionuclides from water. The isotopes Cs 134 and Cs 137 were bioaccumulated by BAC up to 50%, while the I 131 isotope was only physicochemically adsorbed (about 40%). Also, the process of radionuclides (Cs 137 , Ce 139 , Co 57 , Co 60 ) fixation on blue-green algae (Nostoc sp.) was investigated. The kinetics of the removal of these radionuclides from water was recorded. It was found that after a contact period of about half an hour 40-70% of the activity was removed. (Author)

  15. Removal of oil products from fitters in water treatment plants

    Carlson, B.B.; Olander, M.A.; Arvin, E.

    1996-01-01

    Gasoline and oil spills cause aromatic hydrocarbon pollution of ground water. Benzene, toluene and naphtalene can be found in water wells. The purpose of the experiment was to investigate the filtering of water and biological degradation of aromatics on water treatment filters. These filters were proved to reduce benzene, toluene and naphtalene concentration from 5-12 μg/l to 0,3-0,6 μg/l (86-98 % removal). (EG)

  16. Effect of color removal agent on textiles waste water

    Khomsaton Abu Bakar; Selambakknu, Sarala; Jamaliah Shariff; Ting, Teo Ming; Khairul Zaman Dahlan

    2010-01-01

    The effect of color removal agent (CRA) on textile waste water has been studied. The aim of this work is to determine the optimum condition for CRA to react on the textile waste water and to see the effect of CRA on waste water with different Chemical Oxygen Demand. 8 ml CRA was used to treat 800 mls of sample with various COD ranging between 2500 mg/ l-500 mg/ l. The results showed that CRA totally remove the colour of textile waste water at pH ranging from 6 to 8. At an optimum condition CRA works efficiently on waste water with COD 2300 mg/ l for reduction of suspended solid and turbidity. It also observed, sludge accumulation was depended on COD concentration. Color removal curves for different initial COD concentration also obtained. (author)

  17. Electric dipole moments of nanosolvated acid molecules in water clusters.

    Guggemos, Nicholas; Slavíček, Petr; Kresin, Vitaly V

    2015-01-30

    The electric dipole moments of (H2O)nDCl (n=3-9) clusters have been measured by the beam-deflection method. Reflecting the (dynamical) charge distribution within the system, the dipole moment contributes information about the microscopic structure of nanoscale solvation. The addition of a DCl molecule to a water cluster results in a strongly enhanced susceptibility. There is evidence for a noticeable rise in the dipole moment occurring at n≈5-6. This size is consistent with predictions for the onset of ionic dissociation. Additionally, a molecular-dynamics model suggests that even with a nominally bound impurity an enhanced dipole moment can arise due to the thermal and zero-point motion of the proton and the water molecules. The experimental measurements and the calculations draw attention to the importance of fluctuations in defining the polarity of water-based nanoclusters and generally to the essential role played by motional effects in determining the response of fluxional nanoscale systems under realistic conditions.

  18. Hydrogen bonding characterization in water and small molecules

    Silvestrelli, Pier Luigi

    2017-06-01

    The prototypical hydrogen bond in water dimer and hydrogen bonds in the protonated water dimer, in other small molecules, in water cyclic clusters, and in ice, covering a wide range of bond strengths, are theoretically investigated by first-principles calculations based on density functional theory, considering not only a standard generalized gradient approximation functional but also, for the water dimer, hybrid and van der Waals corrected functionals. We compute structural, energetic, and electrostatic (induced molecular dipole moments) properties. In particular, hydrogen bonds are characterized in terms of differential electron density distributions and profiles, and of the shifts of the centres of maximally localized Wannier functions. The information from the latter quantities can be conveyed to a single geometric bonding parameter that appears to be correlated with the Mayer bond order parameter and can be taken as an estimate of the covalent contribution to the hydrogen bond. By considering the water trimer, the cyclic water hexamer, and the hexagonal phase of ice, we also elucidate the importance of cooperative/anticooperative effects in hydrogen-bonding formation.

  19. Escherichia Coli Removal from Water Using Electrophotocatalytic ...

    Michael Horsfall

    inactivation of bacterial microorganisms in areas with low ... disinfection of water contaminated with fecal indicators such as E. coli ... media, brain heart infusion, sodium chloride, sodium hydroxide ... furnace at temperature 105 and 320°C f0r 60 min. For 2- and .... charge of E. coli logarithmic growth phase might affect the ...

  20. Continuum simulations of water flow past fullerene molecules

    Popadic, A.; Praprotnik, M.; Koumoutsakos, P.

    2015-01-01

    We present continuum simulations of water flow past fullerene molecules. The governing Navier-Stokes equations are complemented with the Navier slip boundary condition with a slip length that is extracted from related molecular dynamics simulations. We find that several quantities of interest...... as computed by the present model are in good agreement with results from atomistic and atomistic-continuum simulations at a fraction of the cost. We simulate the flow past a single fullerene and an array of fullerenes and demonstrate that such nanoscale flows can be computed efficiently by continuum flow...

  1. Selective control of photodissociation in deutereted water molecule HOD

    Adhikari, S.; Deshpande, Sarin; Sarma, Manabendra; Kurkal, Vandana; Mishra, M.K.

    2006-01-01

    Bond dissociation in the deutereted water molecule HOD has been investigated to explore the possibility of selective control of dissociation of O-H and O-D bonds using simple field profiles and initial states that do not require high overtone excitations. Preliminary results indicate that considerable selectivity in dissociation of O-H and O-D bonds can be achieved using fundamental and first overtone excitations only and use of field optimized initial state (FOIST) based scheme with appropriate choice of field parameters and initial states may enhance both selectivity and yield

  2. Removal performance and water quality analysis of paper machine white water in a full-scale wastewater treatment plant.

    Shi, Shuai; Wang, Can; Fang, Shuai; Jia, Minghao; Li, Xiaoguang

    2017-06-01

    Paper machine white water is generally characterized as a high concentration of suspended solids and organic matters. A combined physicochemical-biological and filtration process was used in the study for removing pollutants in the wastewater. The removal efficiency of the pollutant in physicochemical and biological process was evaluated, respectively. Furthermore, advanced technology was used to analyse the water quality before and after the process treatment. Experimental results showed that the removal efficiency of suspend solids (SS) of the system was above 99%, while the physicochemical treatment in the forepart of the system had achieved about 97%. The removal efficiency of chemical oxygen demand (COD) and colour had the similar trend after physicochemical treatment and were corresponding to the proportion of suspended and the near-colloidal organic matter in the wastewater. After biological treatment, the removal efficiency of COD and colour achieved were about 97% and 90%, respectively. Furthermore, molecular weight (MW) distribution analysis showed that after treatment low MW molecules (analysis showed that most humic-like substances were effectively removed during the treatment. The analyses of gas chromatography/mass spectrometry showed that the composition of organic matter in the wastewater was not complicated. Methylsiloxanes were the typical organic components in the raw wastewater and most of them were removed after treatment.

  3. Removal of gadolinium nitrate from heavy water

    Wilde, E.W.

    2000-03-22

    Work was conducted to develop a cost-effective process to purify 181 55-gallon drums containing spent heavy water moderator (D2O) contaminated with high concentrations of gadolinium nitrate, a chemical used as a neutron poison during former nuclear reactor operations at the Savannah River Site (SRS). These drums also contain low level radioactive contamination, including tritium, which complicates treatment options. Presently, the drums of degraded moderator are being stored on site. It was suggested that a process utilizing biological mechanisms could potentially lower the total cost of heavy water purification by allowing the use of smaller equipment with less product loss and a reduction in the quantity of secondary waste materials produced by the current baseline process (ion exchange).

  4. Removal of Pesticides From Water by Nanofiltration

    RIUNGU, N J; HESAMPOUR, M; PIHLAJAMAKI, A; MANTTARI, M; home, P G; NDEGWA, G M

    2012-01-01

    Agricultural activities form the backborne of Kenyas economy. Inorder to control crop losses, pesticides are used and in the recent past, more of the pesticides have been used to increase production. However, the effect of pesticides on the environment is very complex as undesirable transfers occur continually among different environmental sections. This eventually leads to contamination of drinking water source especially for rivers and lakes located near active agriculture practices especia...

  5. Removal of phenol from water : a comparison of energization methods

    Grabowski, L.R.; Veldhuizen, van E.M.; Rutgers, W.R.

    2005-01-01

    Direct electrical energization methods for removal of persistent substances from water are under investigation in the framework of the ytriD-project. The emphasis of the first stage of the project is the energy efficiency. A comparison is made between a batch reactor with a thin layer of water and

  6. USE OF SYNTHETIC ZEOLITES FOR ARSENATE REMOVAL FROM POLLUTANT WATER

    Arsenic is known to be a hazardous contaminant in drinking water that causes arsenical dermatitis and skin cancer. In the present work, the potential use of a variety of synthetic zeolites for removal of arsenic from water below the current and proposed EPA MCL has been examined...

  7. 40 CFR 1065.659 - Removed water correction.

    2010-07-01

    ... water content according to paragraph (b)(1) of this section. (3) You may also use a nominal value of...) Use any of the techniques described in paragraph (b) of this section. (2) If the measurement comes.... (a) If you remove water upstream of a concentration measurement, x, or upstream of a flow measurement...

  8. Turbidity removal from surface water using Tamarindus indica crude ...

    Plant-based coagulants are potential alternatives to chemical coagulants used in drinking water treatment. This paper examined the turbidity removal efficiency of Tamarindus indica fruit crude pulp extract (CPE) towards evaluating a low-cost option for drinking-water treatment. Laboratory analysis was carried out on high ...

  9. Process for removing sulfate anions from waste water

    Nilsen, David N.; Galvan, Gloria J.; Hundley, Gary L.; Wright, John B.

    1997-01-01

    A liquid emulsion membrane process for removing sulfate anions from waste water is disclosed. The liquid emulsion membrane process includes the steps of: (a) providing a liquid emulsion formed from an aqueous strip solution and an organic phase that contains an extractant capable of removing sulfate anions from waste water; (b) dispersing the liquid emulsion in globule form into a quantity of waste water containing sulfate anions to allow the organic phase in each globule of the emulsion to extract and absorb sulfate anions from the waste water and (c) separating the emulsion including its organic phase and absorbed sulfate anions from the waste water to provide waste water containing substantially no sulfate anions.

  10. Molecular dynamics study of water molecule diffusion in oil-paper insulation materials

    Liao Ruijin; Zhu Mengzhao; Yang Lijun; Zhou Xin; Gong Chunyan

    2011-01-01

    Moisture is an important factor that influences the safe operation of transformers. In this study, molecular dynamics was employed to investigate the diffusion behavior of water molecules in the oil-paper insulation materials of transformers. Two oil-cellulose models were built. In the first model, water molecules were initially distributed in oil, and in the second model, water molecules were distributed in cellulose. The non-bonding energies of interaction between water molecules and oil, and between water molecules and cellulose, were calculated by the Dreiding force field. The interaction energy was found to play a dominant role in influencing the equilibrium distribution of water molecules. The radial direction functions of water molecules toward oil and cellulose indicate that the hydrogen bonds between water molecules and cellulose are sufficiently strong to withstand the operating temperature of the transformer. Mean-square displacement analysis of water molecules diffusion suggests that water molecules initially distributed in oil showed anisotropic diffusion; they tended to diffuse toward cellulose. Water molecules initially distributed in cellulose diffused isotropically. This study provides a theoretical contribution for improvements in online monitoring of water in transformers, and for subsequent research on new insulation materials.

  11. Molecular dynamics study of water molecule diffusion in oil-paper insulation materials

    Liao Ruijin [State Key Laboratory of Power Transmission Equipment and System Security and New Technology, Chongqing University, Chongqing 400044 (China); Zhu Mengzhao, E-mail: xiaozhupost@163.co [State Key Laboratory of Power Transmission Equipment and System Security and New Technology, Chongqing University, Chongqing 400044 (China); Yang Lijun; Zhou Xin; Gong Chunyan [State Key Laboratory of Power Transmission Equipment and System Security and New Technology, Chongqing University, Chongqing 400044 (China)

    2011-03-01

    Moisture is an important factor that influences the safe operation of transformers. In this study, molecular dynamics was employed to investigate the diffusion behavior of water molecules in the oil-paper insulation materials of transformers. Two oil-cellulose models were built. In the first model, water molecules were initially distributed in oil, and in the second model, water molecules were distributed in cellulose. The non-bonding energies of interaction between water molecules and oil, and between water molecules and cellulose, were calculated by the Dreiding force field. The interaction energy was found to play a dominant role in influencing the equilibrium distribution of water molecules. The radial direction functions of water molecules toward oil and cellulose indicate that the hydrogen bonds between water molecules and cellulose are sufficiently strong to withstand the operating temperature of the transformer. Mean-square displacement analysis of water molecules diffusion suggests that water molecules initially distributed in oil showed anisotropic diffusion; they tended to diffuse toward cellulose. Water molecules initially distributed in cellulose diffused isotropically. This study provides a theoretical contribution for improvements in online monitoring of water in transformers, and for subsequent research on new insulation materials.

  12. Heavy metal removal from waste waters by ion flotation

    Polat, Hürriyet; Erdoğan, D.

    2007-01-01

    Flotation studies were carried out to investigate the removal of heavy metals such as copper (II), zinc (II), chromium (III) and silver (I) from waste waters. Various parameters such as pH, collector and frother concentrations and airflow rate were tested to determine the optimum flotation conditions. Sodium dodecyl sulfate and hexadecyltrimethyl ammonium bromide were used as collectors. Ethanol and methyl isobutyl carbinol (MIBC) were used as frothers. Metal removal reached about 74% under o...

  13. Removal of arsenic from drinking water by natural adsorbents

    MD SHAHNOOR ALAM KHAN

    2017-01-01

    The presence of arsenic in groundwater has been reported in many countries across the world and it is a serious threat to public health. The aim of this study was to identify prospective natural materials with high arsenic adsorption capacity and durable hydraulic property to produce adequate flow of water. The comparative study identified Skye sand as the best natural adsorbent. The prototype household filter with Skye sand achieved complete removal of arsenic and iron. Arsenic removal by du...

  14. Treatment technology for removing radon from small community water supplies

    Kinner, N.E.; Quern, P.A.; Schell, G.S.; Lessard, C.E.; Clement, J.A.

    1990-01-01

    This paper reports on the selection of an appropriate treatment system to remove radon from drinking water which depends primarily upon percent removal; capital and operating and maintenance costs; safety; raw water quality with respect to parameters such as Fe, Mn, bacteria, and organics. The radon removal efficiency of the diffused bubble and packed tower aeration exceeded 99% at A:W ratios of 15:1 and 5:1, respectively; the GAC system averaged 81 ± 7.7%. Though our field evaluations indicated that GAC systems may not be as efficient as aeration systems, the system tested was operated above design requirements for most of the study period. Other researchers have found removals of greater than 99% with GAC point-of-entry applications. Therefore, each of these processes has the potential to consistently remove 99% of the radon applied. However, even this percent removal may not be sufficient to meet an MCL in the range of 200 to 1000 pCi/L if the raw water contained more than 20,000 to 100,000 pCi/L, respectively

  15. Computational study of ibuprofen removal from water by adsorption in realistic activated carbons.

    Bahamon, Daniel; Carro, Leticia; Guri, Sonia; Vega, Lourdes F

    2017-07-15

    Molecular simulations using the Grand Canonical Monte Carlo (GCMC) method have been performed in order to obtain physical insights on how the interaction between ibuprofen (IBP) and activated carbons (ACs) in aqueous mixtures affects IBP removal from water by ACs. A nanoporous carbon model based on units of polyaromatic molecules with different number of rings, defects and polar-oxygenated sites is described. Individual effects of factors such as porous features and chemical heterogeneities in the adsorbents are investigated and quantified. Results are in good agreement with experimental adsorption data, highlightening the ability of GCMC simulation to describe the macroscopic adsorption performance in drug removal applications, while also providing additional insights into the IBP/water adsorption mechanism. The simulation results allow finding the optimal type of activated carbon material for separating this pollutant in water treatment. Copyright © 2017 Elsevier Inc. All rights reserved.

  16. Novel Photocatalytic Reactor Development for Removal of Hydrocarbons from Water

    Morgan Adams

    2008-01-01

    Full Text Available Hydrocarbons contamination of the marine environment generated by the offshore oil and gas industry is generated from a number of sources including oil contaminated drill cuttings and produced waters. The removal of hydrocarbons from both these sources is one of the most significant challenges facing this sector as it moves towards zero emissions. The application of a number of techniques which have been used to successfully destroy hydrocarbons in produced water and waste water effluents has previously been reported. This paper reports the application of semiconductor photocatalysis as a final polishing step for the removal of hydrocarbons from two waste effluent sources. Two reactor concepts were considered: a simple flat plate immobilised film unit, and a new rotating drum photocatalytic reactor. Both units proved to be effective in removing residual hydrocarbons from the effluent with the drum reactor reducing the hydrocarbon content by 90% under 10 minutes.

  17. Mixed Matrix Composite Membranes Containing POSS Molecules for Carbon Dioxide Removal Application

    Rini, Eki Listya

    2011-05-10

    CO2 removal by membrane processes is considerably potential for several applications such as natural gas and synthesis gas purification, enhanced oil recovery application, and carbon dioxide capture in combat against global warming. Dense polymeric membranes are commonly utilized for these type of gas separation applications. Nevertheless, the intrinsic properties of dense polymeric membranes, which commonly characterize by the low gas permeability versus high gas selectivity trade–off or vice versa, is less desirable. In order to meet the increased demand of CO2 removal, a strategy to improve the gas separation performance of a polymeric membrane is investigated in this study. With this regard, mixed matrix membranes in which inorganic non porous fillers are incorporated into a polymeric matrix were prepared to achieve the aforementioned objective. The mixed matrix membranes were prepared from Pebax® block copolymers and PEG POSS® molecules. These hybrid membranes were formed as both dense and multilayer composite membranes. The dense transparent membranes with well–dispersed fillers could be obtained by variation of the solvent mixture. The DSC analyses showed that incorporation of PEG POSS® into Pebax® matrix altered the thermal properties of the matrix. The multilayer composite membranes were then prepared from a PTMSP gutter layer deposited on a PAN porous support and an adjacent hybrid Pebax®/PEG POSS® as the top layer. These hybrid multilayer composite membranes exhibited an enhanced CO2 selectiv4 ity by a factor of two relative to the pure Pebax®. In these hybrid systems, the CO2 separation was presumably enhanced by the high ether oxides content from PEG POSS® that has high affinities for CO2. For particular composition of Pebax® and PEG POSS® concentrations, the PTMSP gutter layer harnessed the CO2 selectivity without losing the CO2 permeation rate. At the same time, these membrane, however, suffered severe adhesion between the gutter layer

  18. PHOSPHATES REMOVAL FROM REJECT WATER FROM DIGESTION OF SLUDGE

    Elżbieta Sperczyńska

    2016-06-01

    Full Text Available The aim of the research work was to evaluate if coagulants used on technical scale are useful in phosphates removal from reject water. Effectiveness of phosphorus compounds removal from reject water from digestion of sewage sludge was examined. Selected prehydrolysed alkaline aluminium polychlorides were used. The results were compared to the ones obtained with aluminium sulphate. Reject water from digestion of sewage sludge form WWTP of 100 000 PE were examined. Commercial agents – prehydrolysed PAX 18, PAX XL10, PAX-XL1905 as well as aluminium sulphate were used. Various doses of coagulants: 0.7; 1.0; 1.5 – time higher than stoichiometric dose were applied. Stoichiometric dose was calculated based on chemical reaction of insoluble aluminium phosphate formation. Concentrations of Kiejdahl nitrogen (891 mgNKj/dm3, phosphates (125 mgPO43-/dm3 and organic compounds - COD (592 mgO2/dm3 in reject water were very high. The effectiveness of coagulation process increased as the doses of chemical agents increased. The most effective doses were the highest ones used during the experiment. The most effective agent was PAX 18 (96% removal efficiency. As the phosphates concentration decreased COD content declined simultaneously. Maximum COD removal (47% was obtained when highly alkaline PAX XL 1905 was used. Use of the lowest dose of Al2(SO43 allowed for 50% phosphates removal, whereas the lowest dose of PAX 18 decreased phosphates concentration by 83%.

  19. Fluoride Removal from Water by Reverse Osmosis Membrane

    Sara Namavar

    2013-09-01

    Full Text Available As fluoride concentration in drinking water is one of the effective parameters in human health, finding the way to remove excess amount of fluoride from drinking water is very important in water supply projects. Today, with developing in technology and finding new methods, the use of membrane technology for producing fresh water get improved. In this study the efficiency of reverse osmosis method to remove fluoride from water was investigated. Initial concentration of fluoride, sulfate and electrical conductivity in feed water and the effect of associated cation with fluoride ion were studied. All tests adapted from “Standard Methods for Examination of Water and Wastewater”. Determination of fluoride concentration was done according the standard SPANDS method by using a spectrophotometer DR/5000. Obtain results show that with increasing in concentration of fluoride and sulfate and electrical conductivity in feed water the efficiency of RO membrane to remove fluoride reduced. In addition, this efficiency for CaF2 was higher than NaF.

  20. Molecular multipole moments of water molecules in ice Ih

    Batista, E.R.; Xantheas, S.S.; Jonsson, H.

    1998-01-01

    We have used an induction model including dipole, dipole endash quadrupole, quadrupole endash quadrupole polarizability and first hyperpolarizability as well as fixed octopole and hexadecapole moments to study the electric field in ice. The self-consistent induction calculations gave an average total dipole moment of 3.09 D, a 67% increase over the dipole moment of an isolated water molecule. A previous, more approximate induction model study by Coulson and Eisenberg [Proc. R. Soc. Lond. A 291, 445 (1966)] suggested a significantly smaller average value of 2.6 D. This value has been used extensively in recent years as a reference point in the development of various polarizable interaction potentials for water as well as for assessment of the convergence of water cluster properties to those of bulk. The reason for this difference is not due to approximations made in the computational scheme of Coulson and Eisenberg but rather due to the use of less accurate values for the molecular multipoles in these earlier calculations. copyright 1998 American Institute of Physics

  1. Colloids removal from water resources using natural coagulant: Acacia auriculiformis

    Abdullah, M.; Roslan, A.; Kamarulzaman, M. F. H.; Erat, M. M.

    2017-09-01

    All waters, especially surface waters contain dissolved, suspended particles and/or inorganic matter, as well as several biological organisms, such as bacteria, algae or viruses. This material must be removed because it can affect the water quality that can cause turbidity and colour. The objective of this study is to develop water treatment process from Seri Alam (Johor, Malaysia) lake water resources by using natural coagulant Acacia auriculiformis pods through a jar test experiment. Jar test is designed to show the effectiveness of the water treatment. This process is a laboratory procedure that will simulate coagulation/flocculation with several parameters selected namely contact time, coagulant dosage and agitation speed. The most optimum percentage of colloids removal for each parameter is determined at 0.2 g, 90 min and 80 rpm. FESEM (Field-emission Scanning Electron Microscope) observed the small structures of final floc particles for optimum parameter in this study to show that the colloids coagulated the coagulant. All result showed that the Acacia auriculiformis pods can be a very efficient coagulant in removing colloids from water.

  2. Uranium removal from water by five aquatic plants

    Hu Nan; Ding Dexin; Li Guangyue; Wang Yongdong; Li Le; Zheng Jifang

    2012-01-01

    Hydroponic solution culture experiments were conducted on the growth of Eichhornia crassipes, Lemna minor L, Azolla imbircata, Potamogeton crispus, and Alligator alternanthera Herb in water with 0.15, 1.50 and 15.00 mg . L -1 concentrations of uranium, and on the uranium removal from the water by the aquatic plants. For the 21 days of hydroponic solution culture experiments, Azolla imbircata exhibited the strongest resistance to uranium and its growth inhibition rates induced by the water with 0.15, 1.50 and 15.00 mg · L -1 concentrations of uranium were 4.56%, 2.48%, 6.79%, respectively, and the uranium removal rates from the water by the plant amounted to 94%, 97% and 92%, respectively. Further experiments revealed that the most uranium removal could be achieved when 7.5 g Azolla imbircata was grown in 1 L of water, and the time required for the plant to reduce the uranium concentration in water with 1.25, 2.50, 5.00 and 10.00 mg · L -l concentrations of uranium below that stipulated in the national emission standards of China were 17, 19, 23 and 25 days, respectively. The results have laid foundation for further studies of phytoremediation of uranium contaminated water. (authors)

  3. Approximative Krieger-Nelkin orientation averaging and anisotropy of water molecules vibrations

    Markovic, M.I.

    1974-01-01

    Quantum-mechanics approach of water molecules dynamics should be taken into account for precise theoretical calculation of differential scattering cross sections of neutrons. Krieger and Nelkin have proposed an approximate method for averaging orientation of molecules regarding directions of incoming and scattered neutron. This paper shows that this approach can be successfully applied for general shape of water molecule vibration anisotropy

  4. Using Iron-Manganese Co-Oxide Filter Film to Remove Ammonium from Surface Water.

    Zhang, Ruifeng; Huang, Tinglin; Wen, Gang; Chen, Yongpan; Cao, Xin; Zhang, Beibei

    2017-07-19

    An iron-manganese co-oxide filter film (MeO x ) has been proven to be a good catalyst for the chemical catalytic oxidation of ammonium in groundwater. Compared with groundwater, surface water is generally used more widely and has characteristics that make ammonium removal more difficult. In this study, MeO x was used to remove ammonium from surface water. It indicated that the average ammonium removal efficiency of MeO x was greater than 90%, even though the water quality changed dramatically and the water temperature was reduced to about 6-8 °C. Then, through inactivating microorganisms, it showed that the removal capability of MeO x included both biological (accounted for about 41.05%) and chemical catalytic oxidation and chemical catalytic oxidation (accounted for about 58.95%). The investigation of the characterizations suggested that MeO x was formed by abiotic ways and the main elements on the surface of MeO x were distributed homogenously. The analysis of the catalytic oxidation process indicated that ammonia nitrogen may interact with MeO x as both ammonia molecules and ammonium ions and the active species of O₂ were possibly • O and O₂ - .

  5. Removal and recovery of tritium from light and heavy water

    Butler, J.P.; Hammerli, M.

    1979-01-01

    A method and apparatus for removing tritium from light water are described, comprising contacting tritiated feed water in a catalyst column in countercurrent flow with hydrogen gas originating from an electrolysis cell so as to enrich this feed water with tritium from the electrolytic hydrogen gas and passing the tritium enriched water to an electrolysis cell wherein the electrolytic hydrogen gas is generated and then fed upwards through the catalyst column or recovered as product. The tritium content of the hydrogen gas leaving the top of the enricher catalyst column is further reduced in a stripper column containing catalyst which transfers the tritium to a countercurrent flow of liquid water. Anodic oxygen and water vapour from the anode compartment may be fed to a drier and condensed electrolyte recycled with a slip stream or recovered as a further tritium product stream. A similar method involving heavy water is also described. (author)

  6. Removal of Arsenic from Drinking Water by Adsorption and Coagulation

    Zhang, M.; Sugita, H.; Hara, J.; Takahashi, S.

    2013-12-01

    Removal of arsenic from drinking water has been an important issue worldwide, which has attracted greater attentions in recent years especially for supplying safe drinking water in developing countries. Although many kinds of treatment approaches that are available or applicable both in principle and practice, such as adsorption, coagulation, membrane filtration, ion exchange, biological process, electrocoagulation and so on, the first 2 approaches (i.e., adsorption and coagulation) are most promising due to the low-cost, high-efficiency, simplicity of treating systems, and thus can be practically used in developing countries. In this study, a literature survey on water quality in Bangladesh was performed to understand the ranges of arsenic concentration and pH of groundwater in Bangladesh. A series of tests were then organized and performed to investigate the effects of arsenic concentration, arsenic forms, pH, chemical compositions of the materials used for adsorption and coagulation, particle size distribution and treatment time on quality of treated water. The experimental results obtained in the study illustrated that both adsorption and coagulation can be used to effectively reduce the concentrations of either arsenic (V) or arsenic (III) from the contaminated water. Coagulation of arsenic with a magnesium-based material developed in this study can be very effective to remove arsenic, especially arsenic (V), from contaminated water with a concentration of 10 ppm to an undetectable level of 0.002 ppm by ICP analyses. Compared to arsenic (III), arsenic (V) is easier to be removed. The materials used for adsorption and coagulation in this study can remove arsenic (V) up to 9 mg/g and 6 mg/g, and arsenic (III) up to 4 mg/g and 3 mg/g, respectively, depending on test conditions and compositions of the materials being used. The control of pH during treatment can be a challenging technical issue for developing both adsorbent and coagulant. Keywords: Water Treatment

  7. Removal of some radionuclides from water by bioaccumulation

    Miskovic, D.; Conkic, L.; Dalmacija, B.; Gantar, M. (Trg D. Obradvica 3, Novi Sad (Yugoslavia). Faculty of Sciences)

    1992-01-01

    First objective of this study was to investigate the application of biologically activated carbon (BAC) as well as its comparison to adsorption, with the aim of removing some radionuclides from water. The isotopes Cs[sup 134] and Cs[sup 137] were bioaccumulated by BAC up to 50%, while the I[sup 131] isotope was only physicochemically adsorbed (about 40%). Also, the process of radionuclides (Cs[sup 137], Ce[sup 139], Co[sup 57], Co[sup 60]) fixation on blue-green algae (Nostoc sp.) was investigated. The kinetics of the removal of these radionuclides from water was recorded. It was found that after a contact period of about half an hour 40-70% of the activity was removed. (Author).

  8. Fluoride removal studies in water using natural materials : technical ...

    Excess fluoride in water causes health hazards to the natural environment. The removal of fluoride was attempted using natural materials such as red soil, charcoal, brick, fly-ash and serpentine. Each material was set up in a column for a known volume and the defluoridation capacities of these materials were studied with ...

  9. Fluoride removal from rural spring water using wood ash

    Makhado, R

    2006-05-01

    Full Text Available This paper presents an overview of a report on an investigation on the use of cheap wood ash as an effective means of removing excess fluoride from drinking water used by an impoverished rural community of the Didi village in Limpopo province....

  10. Removal of organic compounds from shale gas flowback water

    Butkovskyi, Andrii; Faber, Ann-Hélène; Wang, Yue; Grolle, Katja; Hofman-Caris, Roberta; Bruning, Harry; Van Wezel, Annemarie P.; Rijnaarts, Huub H M

    2018-01-01

    Ozonation, sorption to granular activated carbon and aerobic degradation were compared as potential treatment methods for removal of dissolved organic carbon (DOC) fractions and selected organic compounds from shale gas flowback water after pre-treatment in dissolved air flotation unit. Flowback

  11. Removal of antibiotics from surface and distilled water in conventional water treatment processes

    Adams, C.; Wang, Y.; Loftin, K.; Meyer, M.

    2002-01-01

    Conventional drinking water treatment processes were evaluated under typical water treatment plant conditions to determine their effectiveness in the removal of seven common antibiotics: carbadox, sulfachlorpyridazine, sulfadimethoxine, sulfamerazine, sulfamethazine, sulfathiazole, and trimethoprim. Experiments were conducted using synthetic solutions prepared by spiking both distilled/ deionized water and Missouri River water with the studied compounds. Sorption on Calgon WPH powdered activated carbon, reverse osmosis, and oxidation with chlorine and ozone under typical plant conditions were all shown to be effective in removing the studied antibiotics. Conversely, coagulation/flocculation/sedimentation with alum and iron salts, excess lime/soda ash softening, ultraviolet irradiation at disinfection dosages, and ion exchange were all relatively ineffective methods of antibiotic removal. This study shows that the studied antibiotics could be effectively removed using processes already in use many water treatment plants. Additional work is needed on by-product formation and the removal of other classes of antibiotics.

  12. Carbon Nanotubes Technology for Removal of Arsenic from Water

    Ali Naghizadeh

    2012-08-01

    Full Text Available Please cite this article as: Naghizadeh A, Yari AR, Tashauoei HR, Mahdavi M, Derakhshani E, Rahimi R, Bahmani P. Carbon nanotubes technology for removal of arsenic from water. Arch Hyg Sci 2012;1(1:6-11. Aims of the Study: This study was aimed to investigate the adsorption mechanism of the arsenic removal from water by using carbon nanotubes in continuous adsorption column. Materials & Methods: Independent variables including carbon nanotubes dosage, contact time and breakthrough point were carried out to determine the influence of these parameters on the adsorption capacity of the arsenic from water. Results: Adsorption capacities of single wall and multiwall carbon nanotubes were about 148 mg/g and 95 mg/g respectively. The experimental data were analyzed using Langmuir and Freundlich isotherm models and equilibrium data indicate the best fit obtained with Langmuir isotherm model. Conclusions: Carbon nanotubes can be considered as a promising adsorbent for the removal of arsenic from large volume of aqueous solutions. References: 1. Lomaquahu ES, Smith AH. Feasibility of new epidemiology studies on arsenic exposures at low levels. AWWA Inorganic Contaminants Workshop. San Antonio; 1998. 2. Burkel RS, Stoll RC. Naturally occurring arsenic in sandstone aquifer water supply wells of North Eastern Wisconsin. Ground Water Monit Remediat 1999;19(2:114-21. 3. Mondal P, Majumder CB, Mohanty B. Laboratory based approaches for arsenic remediation from contaminated water: recent developments. J Hazard Mater 2006;137(1: 464-79. 4. Meenakshi RCM. Arsenic removal from water: a review. Asian J Water Environ Pollut 2006;3(1:133-9. 5. Wickramasinghe SR, Binbing H, Zimbron J, Shen Z, Karim MN. Arsenic removal by coagulation and filtration: comparison of ground waters from United States and Bangladesh. Desalination 2004;169:231-44. 6. Hossain MF. Arsenic contamination in Bangladesh-an overview. Agric Ecosyst Environ 2006;113(1-4:1-16. 7. USEPA, Arsenic. Final

  13. Pollutants in drinking water - sources, harmful effects and removal procedures

    Qadeer, R.

    2005-01-01

    The underground water resources available for human consumption are being continuously contaminated by the natural sources and anthropogenic activities. The pollutants include toxic microorganism, inorganic and organic chemicals and radionuclide etc. This is an acute problem in our country, where free style way of disposal of industrial effluents into the natural water bodies contaminates the surface and ground water. These contaminants make their way into human body through contaminated drinking water, which leads to the malfunctioning of the body organs. Details of some pollutants present in drinking water, their source and harmful effects on human beings are reviewed in this communication Merits and demerits of methods used to remove the pollutants from drinking water are also discussed. (author)

  14. Sorbents for phosphate removal from agricultural drainage water

    Lyngsie, Gry

    Subsurface transport of phosphate (P) from fertilized agricultural fields to freshwaters may lead to eutrophication and reduced biodiversity in inland waters. Mitigation of eutrophic waters is difficult and costly. Reduction of P export to surface waters using filters installed in agricultural...... drains comprising P sorbing materials (PSM) may be a more efficient and cost-effective way to improve water quality. Several materials have been proposed as PSMs for use for cleaning agricultural drainage water. The objective of the present study was to provide data on sorption behavior among a variety...... of PSMs in order to select a material that can quickly remove P from runoff water at both base and peak flow. This was done by screening 15 “local” PSMs’ for their ability to sorb and retain low orthophosphate concentrations (0-161 µM) at short equilibration time (

  15. Distribution of binding energies of a water molecule in the water liquid-vapor interface

    Chempath, Shaji [Los Alamos National Laboratory; Pratt, Lawrence R [TULANE UNIV

    2008-01-01

    Distributions of binding energies of a water molecule in the water liquid-vapor interface are obtained on the basis of molecular simulation with the SPC/E model of water. These binding energies together with the observed interfacial density profile are used to test a minimally conditioned Gaussian quasi-chemical statistical thermodynamic theory. Binding energy distributions for water molecules in that interfacial region clearly exhibit a composite structure. A minimally conditioned Gaussian quasi-chemical model that is accurate for the free energy of bulk liquid water breaks down for water molecules in the liquid-vapor interfacial region. This breakdown is associated with the fact that this minimally conditioned Gaussian model would be inaccurate for the statistical thermodynamics of a dilute gas. Aggressive conditioning greatly improves the performance of that Gaussian quasi-chemical model. The analogy between the Gaussian quasi-chemical model and dielectric models of hydration free energies suggests that naive dielectric models without the conditioning features of quasi-chemical theory will be unreliable for these interfacial problems. Multi-Gaussian models that address the composite nature of the binding energy distributions observed in the interfacial region might provide a mechanism for correcting dielectric models for practical applications.

  16. Alternative technology for arsenic removal from drinking water

    Purenović Milovan

    2007-01-01

    Full Text Available Arsenic is a naturally occurring element in water, food and air. It is known as a poison, but in very small quantities it is showed to be an essential element. Actual problem in the world is arsenic removal from drinking water using modern and alternative technology, especially because EPA's and other international standards have reduced MCL from 50 to 10 ug/1. Because of rivers and lakes pollution, in a number of plants for natural water purification, average concentrations of arsenic in water are up to 100 ug/1. According to MCL, present technologies are unadjusted for safely arsenic removal for concentrations below of 10 ug/1. This fact has inspired many companies to solve this problem adequately, by using an alternative technologies and new process able materials. In this paper the observation of conventional and the alternative technologies will be given, bearing in mind complex chemistry and electrochemistry of arsenic, formation of colloidal arsenic, which causes the biggest problems in water purification technologies. In this paper many results will be presented, which are obtained using the alternative technologies, as well as the newest results of original author's investigations. Using new nanomaterials, on Pilot plant "VALETA H2O-92", concentration of arsenic was removed far below MLC value.

  17. Removal of organic pollutants from produced water using Fenton oxidation

    Afzal Talia

    2018-01-01

    Full Text Available Produced water (PW is the largest stream of wastewater from oil and gas exploration. It is highly polluted and requires proper treatment before disposal. The main objective of this study was to investigate the effectiveness of Fenton oxidation in degradation of organic matter in PW. The role of operating factors viz., H2O2 concentration (0.12 × 10-3 moles/L to 3 moles/L, [H2O2]/[Fe2+] molar ratio (2 to 75, and reaction time (30 to 200 minutes, on COD removal was determined through a series of batch experiments conducted in acidic environment at room temperature. The experiments were conducted with 500 mL PW samples in 1L glass beakers covered on the outside with aluminum foil to protect them from sunlight. Pre-decided amounts of ferrous sulfate heptahydrate (FeSO4.7H2O and hydrogen peroxide (H2O2 were added to initiate the Fenton reaction. An increase in COD removal was observed with increase in reaction time and [H2O2]/[Fe2+] molar ratio. COD removal also increased with H2O2 concentration up to 0.01 moles/L; further increase in H2O2 concentration decreased the COD removal efficiency. Over 90% COD removal was achieved under optimum reaction conditions. The study indicates that Fenton oxidation is effective for remediation of PW in terms of organic matter removal.

  18. Removal of organic pollutants from produced water using Fenton oxidation

    Afzal, Talia; Hasnain Isa, Mohamed; Mustafa, Muhammad Raza ul

    2018-03-01

    Produced water (PW) is the largest stream of wastewater from oil and gas exploration. It is highly polluted and requires proper treatment before disposal. The main objective of this study was to investigate the effectiveness of Fenton oxidation in degradation of organic matter in PW. The role of operating factors viz., H2O2 concentration (0.12 × 10-3 moles/L to 3 moles/L), [H2O2]/[Fe2+] molar ratio (2 to 75), and reaction time (30 to 200 minutes), on COD removal was determined through a series of batch experiments conducted in acidic environment at room temperature. The experiments were conducted with 500 mL PW samples in 1L glass beakers covered on the outside with aluminum foil to protect them from sunlight. Pre-decided amounts of ferrous sulfate heptahydrate (FeSO4.7H2O) and hydrogen peroxide (H2O2) were added to initiate the Fenton reaction. An increase in COD removal was observed with increase in reaction time and [H2O2]/[Fe2+] molar ratio. COD removal also increased with H2O2 concentration up to 0.01 moles/L; further increase in H2O2 concentration decreased the COD removal efficiency. Over 90% COD removal was achieved under optimum reaction conditions. The study indicates that Fenton oxidation is effective for remediation of PW in terms of organic matter removal.

  19. Zeolites for nitrosamine and pharmaceutical removal from demineralised and surface water: Mechanisms and efficacy

    De Ridder, David J.

    2012-03-01

    Zeolites with a high Si/Al ratio can be used as selective adsorbents in water treatment, targeting organic micropollutants which are removed poorly with activated carbon. Due to size exclusion, many Natural Organic Matter (NOM) components cannot access the pores, thus limiting adsorption competition between organic micropollutant and NOM. Furthermore, zeolite channel diameters are close to molecule diameters, which results in strong van der Waals interaction. MOR200 and ZSM5, the two most hydrophobic zeolites, showed the highest removal of neutral nitrosamines in demineralised water, with higher efficacy than activated carbon. DAY and MOR30, which were relatively hydrophilic zeolites, did not show appreciable removal of any of the nitrosamines. When nitrosamines were adsorbed from surface water, there was no influence of competition with, or pore blockage by, NOM components on nitrosamine removal for ZSM5 zeolite, in contrast to activated carbon. Repulsion of negatively charged pharmaceuticals was significant for ZSM5, which had a Si/Al ratio of 80. MOR200 had a Si/Al ratio of 200, indicating a lower Al content than ZSM5 and, as such, a lower negative surface charge. Charge effects were not observed for MOR200. A relationship was found between the Stokes diameter of the pharmaceuticals and nitrosamines, and their removal by ZSM5 and MOR200, indicating that a "close fit" adsorption mechanism is more likely than hydrophobic interaction in these zeolites. Due to their selective nature, adsorption on zeolites should only be considered as an additional treatment step to existing processes, dedicated for the removal of specific organic micropollutants. Less specific treatment techniques, such as activated carbon filtration, are still required to ensure a broad barrier for organic micropollutants in water treatment. © 2012 Elsevier B.V. All rights reserved.

  20. Experiments on aerosol removal by high-pressure water spray

    Corno, Ada del, E-mail: delcorno@rse-web.it [RSE, Power Generation Technologies and Materials Dept, via Rubattino 54, I-20134 Milano (Italy); Morandi, Sonia, E-mail: morandi@rse-web.it [RSE, Power Generation Technologies and Materials Dept, via Rubattino 54, I-20134 Milano (Italy); Parozzi, Flavio, E-mail: parozzi@rse-web.it [RSE, Power Generation Technologies and Materials Dept, via Rubattino 54, I-20134 Milano (Italy); Araneo, Lucio, E-mail: lucio.araneo@polimi.it [Politecnico di Milano, Department of Energy, via Lambruschini 4A, I-20156 Milano (Italy); CNR-IENI, via Cozzi 53, I-20125 Milano (Italy); Casella, Francesco, E-mail: francesco2.casella@mail.polimi.it [Politecnico di Milano, Department of Energy, via Lambruschini 4A, I-20156 Milano (Italy)

    2017-01-15

    Highlights: • Experimental research to measure the efficiency of high-pressure sprays in capturing aerosols if applied to a filtered containment venting system in case of severe accident. • Cloud of monodispersed SiO{sub 2} particles with sizes 0.5 or 1.0 μm and initial concentration in the range 2–90 mg/m{sup 3}. • Carried out in a chamber 0.5 × 1.0 m and 1.5 m high, with transparent walls equipped with a high pressure water spray with single nozzle. • Respect to low-pressure sprays, removal efficiency turned out significant: the half-life for 1 μm particles with a removal high-pressure spray system is orders of magnitude shorter than that with a low-pressure sprays system. - Abstract: An experimental research was managed in the framework of the PASSAM European Project to measure the efficiency of high-pressure sprays in capturing aerosols when applied to a filtered containment venting system in case of severe accident. The campaign was carried out in a purposely built facility composed by a scrubbing chamber 0.5 × 1.0 m and 1.5 m high, with transparent walls to permit the complete view of the aerosol removal process, where the aerosol was injected to form a cloud of specific particle concentration. The chamber was equipped with a high pressure water spray system with a single nozzle placed on its top. The test matrix consisted in the combination of water pressure injections, in the range 50–130 bar, on a cloud of monodispersed SiO{sub 2} particles with sizes 0.5 or 1.0 μm and initial concentration ranging between 2 and 99 mg/m{sup 3}. The spray was kept running for 2 min and the efficiency of the removal was evaluated, along the test time, using an optical particle sizer. With respect to low-pressure sprays, the removal efficiency turned out much more significant: the half-life for 1 μm particles with a removal high-pressure spray system is orders of magnitude shorter than that with a low-pressure spray system. The highest removal rate was

  1. Removal of Sulfate from Waste Water by Activated Carbon

    Mohammed Sadeq Salman

    2009-01-01

    Activated carbon was Produced from coconut shell and was used for removing sulfate from industrial waste water in batch Processes. The influence of various parameter were studied such as pH (4.5 9.) , agitation time (0 120)min and adsorbent dose (2 10) gm.The Langmuir and frandlich adsorption capacity models were been investigated where showed there are fitting with langmmuir model with squre regression value ( 0.76). The percent of removal of sulfate (22% - 38%) at (PH=7) in the isotherm ...

  2. Heavy metal removal from waste waters by ion flotation.

    Polat, H; Erdogan, D

    2007-09-05

    Flotation studies were carried out to investigate the removal of heavy metals such as copper (II), zinc (II), chromium (III) and silver (I) from waste waters. Various parameters such as pH, collector and frother concentrations and airflow rate were tested to determine the optimum flotation conditions. Sodium dodecyl sulfate and hexadecyltrimethyl ammonium bromide were used as collectors. Ethanol and methyl isobutyl carbinol (MIBC) were used as frothers. Metal removal reached about 74% under optimum conditions at low pH. At basic pH it became as high as 90%, probably due to the contribution from the flotation of metal precipitates.

  3. Experiments on aerosol removal by high-pressure water spray

    Corno, Ada del; Morandi, Sonia; Parozzi, Flavio; Araneo, Lucio; Casella, Francesco

    2017-01-01

    Highlights: • Experimental research to measure the efficiency of high-pressure sprays in capturing aerosols if applied to a filtered containment venting system in case of severe accident. • Cloud of monodispersed SiO_2 particles with sizes 0.5 or 1.0 μm and initial concentration in the range 2–90 mg/m"3. • Carried out in a chamber 0.5 × 1.0 m and 1.5 m high, with transparent walls equipped with a high pressure water spray with single nozzle. • Respect to low-pressure sprays, removal efficiency turned out significant: the half-life for 1 μm particles with a removal high-pressure spray system is orders of magnitude shorter than that with a low-pressure sprays system. - Abstract: An experimental research was managed in the framework of the PASSAM European Project to measure the efficiency of high-pressure sprays in capturing aerosols when applied to a filtered containment venting system in case of severe accident. The campaign was carried out in a purposely built facility composed by a scrubbing chamber 0.5 × 1.0 m and 1.5 m high, with transparent walls to permit the complete view of the aerosol removal process, where the aerosol was injected to form a cloud of specific particle concentration. The chamber was equipped with a high pressure water spray system with a single nozzle placed on its top. The test matrix consisted in the combination of water pressure injections, in the range 50–130 bar, on a cloud of monodispersed SiO_2 particles with sizes 0.5 or 1.0 μm and initial concentration ranging between 2 and 99 mg/m"3. The spray was kept running for 2 min and the efficiency of the removal was evaluated, along the test time, using an optical particle sizer. With respect to low-pressure sprays, the removal efficiency turned out much more significant: the half-life for 1 μm particles with a removal high-pressure spray system is orders of magnitude shorter than that with a low-pressure spray system. The highest removal rate was detected with 1

  4. Biostimulation strategies to enhance manganese removal in drinking water biofilters

    Breda, Inês Lousinha Ribeiro; Ramsay, Loren; Søborg, Ditte

    to national drinking water criteria. The period during which virgin filter media matures into a fully functional biofilter is designated as the start-up period. The duration of a start-up for efficient manganese removal varies from weeks to more than a year. The aim of this study was to investigate...... growth and activity of specific bacteria. Biostimulation of virgin media to enhance initial manganese removal using different amendments strategies is possible especially in the early stages of filter development whereas autocatalytic processes appear to become dominant with time. The complex...

  5. La3+-modified activated alumina for fluoride removal from water

    Cheng, Jiemin; Meng, Xiaoguang; Jing, Chuanyong; Hao, Jumin

    2014-01-01

    Graphical abstract: - Highlights: • A La 3+ -modified activated alumina adsorbent was prepared for effective removal F − . • SEM/EDS and EXAFS analyses determined the formation of La(OH) 3 coating on the AA. • The La-AA had much high adsorption rate and capacity than the AA. • The La-AA was promising adsorbent for effective removal of F − from water. - Abstract: A La 3+ -modified activated alumina (La-AA) adsorbent was prepared for effective removal of fluoride from water. The surface properties of adsorbent were characterized with zeta potential analysis, SEM-EDS and EXAFS. Batch and column experiments were conducted to evaluate improvement of F − removal by the La-AA. SEM/EDS and EXAFS analyses determined the formation of La(OH) 3 coating on the AA and strong bonding interactions between La 3+ and the Al atoms. The points of zero charge (pH PZC ) of AA and La-AA were at pH 8.94 and 9.57, respectively. Batch experimental results indicated that the La-AA had much higher adsorption rate and capacity than the AA. The F − adsorption processes on La-AA and AA followed the pseudo-second-order kinetics and the Langmuir isotherm. Column filtration results shows that the La-AA and AA treated 270 and 170 bed volumes of the F − -spiked tap water, respectively, before F − breakthrough occurred. The results demonstrated that the La-AA was a promising adsorbent for effective removal of F − from water

  6. Rapid and accurate prediction and scoring of water molecules in protein binding sites.

    Gregory A Ross

    Full Text Available Water plays a critical role in ligand-protein interactions. However, it is still challenging to predict accurately not only where water molecules prefer to bind, but also which of those water molecules might be displaceable. The latter is often seen as a route to optimizing affinity of potential drug candidates. Using a protocol we call WaterDock, we show that the freely available AutoDock Vina tool can be used to predict accurately the binding sites of water molecules. WaterDock was validated using data from X-ray crystallography, neutron diffraction and molecular dynamics simulations and correctly predicted 97% of the water molecules in the test set. In addition, we combined data-mining, heuristic and machine learning techniques to develop probabilistic water molecule classifiers. When applied to WaterDock predictions in the Astex Diverse Set of protein ligand complexes, we could identify whether a water molecule was conserved or displaced to an accuracy of 75%. A second model predicted whether water molecules were displaced by polar groups or by non-polar groups to an accuracy of 80%. These results should prove useful for anyone wishing to undertake rational design of new compounds where the displacement of water molecules is being considered as a route to improved affinity.

  7. Laser removal of water repellent treatments on limestone

    Gomez-Heras, Miguel; Alvarez de Buergo, Monica; Rebollar, Esther; Oujja, Mohamed; Castillejo, Marta; Fort, Rafael

    2003-12-15

    Protective and water repellent treatments are applied on stone materials used on buildings or sculptures of artistic value to reduce water intrusion without limiting the natural permeability to water vapour of the material. The effect of the wavelength associated with the laser removal of two water repellent treatments applied on limestone, Paraloid B-72, a copolymer of methyl acrylate and ethyl methacrylate, and Tegosivin HL-100, a modified polysiloxane resin, was investigated by using the four harmonics of a Q-switched Nd:YAG laser (1064, 532, 355 and 266 nm). The modifications induced on the surface of limestone samples by laser irradiation were studied using colorimetry, roughness measurements and scanning electron microscopy (SEM). The removal of the treatments was found to be dependent on the laser irradiation conditions and on the characteristics of the coatings. The fundamental laser radiation was effective in removing both treatments, but thermal alteration processes were induced on the constituent calcite crystals. The best results were obtained by irradiation in the near UV at 355 nm.

  8. Removal of arsenic from contaminated water using coagulation enhanced microfiltration

    Volchek, K.; Velicogna, D.; Dumouchel, A.; Wong, W.P.; Brown, C.E.

    2002-01-01

    Results of an innovative arsenic removal process were presented. The process is based on a combination of coagulation and microfiltration processes. Coagulation-Enhanced Microfiltration (CEMF) may eventually become a full-scale commercial technology. This study focused on the process with respect to groundwater treatment because of the importance of arsenic contamination in drinking water. Most experiments were bench-scale using tap water spiked with arsenic. Ferric chloride, which is commonly used in arsenic removal processes was also added. In addition, some tests were conducted on actual arsenic-contaminated water from the effluent treatment plant of a former mining site in Ontario. Results indicate a high arsenic removal efficiency in both spiked and actual water solutions. The microfiltration significantly reduced the level of arsenic in the treatment. This paper described the characteristics of membrane separation. It also presented information regarding chemically enhanced membrane filtration and coagulation-enhanced microfiltration. Bench-scale tests were conducted with both tubular membranes and with immersed capillary membranes. The effect of iron to arsenic ratios on the effectiveness of the system was also tested. It was recommended that future research should include a field study of the process on a pilot-scale to optimize process parameters and to accurately determine the cost of the process. 16 refs., 8 tabs., 9 figs

  9. Aluminium removal from water after defluoridation with the electrocoagulation process.

    Sinha, Richa; Mathur, Sanjay; Brighu, Urmila

    2015-01-01

    Fluoride is the most electronegative element and has a strong affinity for aluminium. Owing to this fact, most of the techniques used for fluoride removal utilized aluminium compounds, which results in high concentrations of aluminium in treated water. In the present paper, a new approach is presented to meet the WHO guideline for residual aluminium concentration as 0.2 mg/L. In the present work, the electrocoagulation (EC) process was used for fluoride removal. It was found that aluminium content in water increases with an increase in the energy input. Therefore, experiments were optimized for a minimum energy input to achieve the target value (0.7 mg/L) of fluoride in resultant water. These optimized sets were used for further investigations of aluminium control. The experimental investigations revealed that use of bentonite clay as coagulant in clariflocculation brings down the aluminium concentration of water below the WHO guideline. Bentonite dose of 2 g/L was found to be the best for efficient removal of aluminium.

  10. Removing efficiency of radon from water by different methods

    Muellerova, M.; Holy, K.; Gulasova, Z.; Polaskova, A.

    2008-01-01

    In this contribution problem of radon removing from water samples by different methods was tested. Lowest efficiency of deemanation was achieved at tossing of water from one vessel into the other. For increasing of efficiency deemanation of radon use of needle-bath principle was also used. Low efficiency deemanation was found at trapping of radon from sample of water by toluene (83 ± 5) %, too. Reversal highest efficiency deemanation of radon from water was reached at aerating by argon (95 ± 6)%. It is shown, that reduction of volume activity of radon in water under 0.1 Bq/dm l - 3 is big problem. Suppression of this limit will claim use of more completion and sophistic approaches. (author)

  11. Survival of fish upon removal of cyanide from water

    Gacsi, Mariann; Czegeny, Ildiko; Nagy, Gabor; Banfalvi, Gaspar

    2005-01-01

    The effects of potassium cyanide and the removal of cyanide from water in vivo on the survival of fish were investigated. This research was initiated because of the catastrophe that took place at the end of January 2000 in the Carpathian basin, when an enormous amount of cyanide pollution swept through the Samos and Tisza rivers, and then to the Danube. Since nothing was done against the disaster, we have suggested a chemical solution to remove cyanide from waterways (Chem. Innovat. 30 (2000b) 53). Based on experiments, we describe that the most effective and harmless way to remove cyanide and to save the lives of fish from 40 to 160x the lethal doses of cyanide is to use carbogen gas containing 5% carbon dioxide and 95% oxygen followed by aeration with air

  12. A Single-Molecule Propyne Trap: Highly Efficient Removal of Propyne from Propylene with Anion-Pillared Ultramicroporous Materials.

    Yang, Lifeng; Cui, Xili; Yang, Qiwei; Qian, Siheng; Wu, Hui; Bao, Zongbi; Zhang, Zhiguo; Ren, Qilong; Zhou, Wei; Chen, Banglin; Xing, Huabin

    2018-03-01

    Propyne/propylene (C 3 H 4 /C 3 H 6 ) separation is a critical process for the production of polymer-grade C 3 H 6 . However, optimization of the structure of porous materials for the highly efficient removal of C 3 H 4 from C 3 H 6 remains challenging due to their similar structures and ultralow C 3 H 4 concentration. Here, it is first reported that hybrid ultramicroporous materials with pillared inorganic anions (SiF 6 2- = SIFSIX, NbOF 5 2- = NbOFFIVE) can serve as highly selective C 3 H 4 traps for the removal of trace C 3 H 4 from C 3 H 6 . Especially, it is revealed that the pyrazine-based ultramicroporous material with square grid structure for which the pore shape and functional site disposition can be varied in 0.1-0.5 Å scale to match both the shape and interacting sites of guest molecule is an interesting single-molecule trap for C 3 H 4 molecule. The pyrazine-based single-molecule trap enables extremely high C 3 H 4 uptake under ultralow concentration (2.65 mmol g -1 at 3000 ppm, one C 3 H 4 per unit cell) and record selectivity over C 3 H 6 at 298 K (>250). The single-molecule binding mode for C 3 H 4 within ultramicroporous material is validated by X-ray diffraction experiments and modeling studies. The breakthrough experiments confirm that anion-pillared ultramicroporous materials set new benchmarks for the removal of ultralow concentration C 3 H 4 (1000 ppm on SIFSIX-3-Ni, and 10 000 ppm on SIFSIX-2-Cu-i) from C 3 H 6 . © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Removal of arsenic from drinking water using rice husk

    Asif, Zunaira; Chen, Zhi

    2017-06-01

    Rice husk adsorption column method has proved to be a promising solution for arsenic (As) removal over the other conventional methods. The present work investigates the potential of raw rice husk as an adsorbent for the removal of arsenic [As(V)] from drinking water. Effects of various operating parameters such as diameter of column, bed height, flow rate, initial arsenic feed concentration and particle size were investigated using continuous fixed bed column to check the removal efficiency of arsenic. This method shows maximum removal of As, i.e., 90.7 % under the following conditions: rice husk amount 42.5 g; 7 mL/min flow rate in 5 cm diameter column at the bed height of 28 cm for 15 ppb inlet feed concentration. Removal efficiency was increased from 83.4 to 90.7 % by reducing the particle size from 1.18 mm to 710 µm for 15 ppb concentration. Langmuir and Freundlich isotherm models were employed to discuss the adsorption behavior. The effect of different operating parameters on the column adsorption was determined using breakthrough curves. In the present study, three kinetic models Adam-Bohart, Thomas and Yoon-Nelson were applied to find out the saturated concentration, fixed bed adsorption capacity and time required for 50 % adsorbate breakthrough, respectively. At the end, solidification was done for disposal of rice husk.

  14. Membrane Bioprocesses for Pharmaceutical Micropollutant Removal from Waters

    Matthias de Cazes

    2014-10-01

    Full Text Available The purpose of this review work is to give an overview of the research reported on bioprocesses for the treatment of domestic or industrial wastewaters (WW containing pharmaceuticals. Conventional WW treatment technologies are not efficient enough to completely remove all pharmaceuticals from water. Indeed, these compounds are becoming an actual public health problem, because they are more and more present in underground and even in potable waters. Different types of bioprocesses are described in this work: from classical activated sludge systems, which allow the depletion of pharmaceuticals by bio-degradation and adsorption, to enzymatic reactions, which are more focused on the treatment of WW containing a relatively high content of pharmaceuticals and less organic carbon pollution than classical WW. Different aspects concerning the advantages of membrane bioreactors for pharmaceuticals removal are discussed, as well as the more recent studies on enzymatic membrane reactors to the depletion of these recalcitrant compounds.

  15. Radon-removal techniques for small community public water supplies

    Kinner, N.E.; Malley, J.P.; Clement, J.A.; Quern, P.A.; Schell, G.S.

    1990-08-01

    The report presents the results of an evaluation, performed by the University of New Hampshire--Environmental Research Group (ERG), of radon removal in small community water supplies using full-scale granular activated carbon adsorption, diffused bubble aeration and packed tower aeration. Various low technology alternatives, such as loss in a distribution system and addition of coarse bubble aeration to a pilot-scale atmospheric storage tank were also evaluated. The report discusses each of the treatment alternatives with respect to their radon removal efficiency, potential problems (i.e., waste disposal, radiation exposure and intermedia pollution), and economics in small community applications. In addition, several sampling methods, storage times, scintillation cocktails and extraction procedures currently used in the liquid scintillation technique for analysis of radon in water were compared

  16. Removal of uranium from water media by bentonite and zeolite

    Viglasova, E.; Krajnak, A.; Galambos, M.; Rosskopfova, O.

    2014-01-01

    The removal and recovery of uranium from contaminated surface, environment and ground water, as result of nuclear industries, has attracted more and more attentions. Several methods are available for removing of uranium, but adsorption among the others, is the most attractive. In case of management of radioactive waste, the adsorption of radionuclides plays significant role. Among the natural sorbents applied to the adsorption of uranium zeolites and bentonites offer a number of advantages. The main aims of this work are investigations of adsorption properties of Greek zeolite Metaxades and Greek bentonite Kimolos during adsorption of uranium from water solutions, comparison of their adsorption characteristics, fitting with isotherms (Freundlich, Langmuir and DR isotherm) and its behaviour during kinetics process influenced by temperature. (authors)

  17. Fast Rotational Diffusion of Water Molecules in a 2D Hydrogen Bond Network at Cryogenic Temperatures

    Prisk, T. R.; Hoffmann, C.; Kolesnikov, A. I.; Mamontov, E.; Podlesnyak, A. A.; Wang, X.; Kent, P. R. C.; Anovitz, L. M.

    2018-05-01

    Individual water molecules or small clusters of water molecules contained within microporous minerals present an extreme case of confinement where the local structure of hydrogen bond networks are dramatically altered from bulk water. In the zinc silicate hemimorphite, the water molecules form a two-dimensional hydrogen bond network with hydroxyl groups in the crystal framework. Here, we present a combined experimental and theoretical study of the structure and dynamics of water molecules within this network. The water molecules undergo a continuous phase transition in their orientational configuration analogous to a two-dimensional Ising model. The incoherent dynamic structure factor reveals two thermally activated relaxation processes, one on a subpicosecond timescale and another on a 10-100 ps timescale, between 70 and 130 K. The slow process is an in-plane reorientation of the water molecule involving the breaking of hydrogen bonds with a framework that, despite the low temperatures involved, is analogous to rotational diffusion of water molecules in the bulk liquid. The fast process is a localized motion of the water molecule with no apparent analogs among known bulk or confined phases of water.

  18. Clinoptilolite in Drinking Water Treatment for Ammonia Removal

    H. M. Abd El-Hady

    2001-01-01

    Full Text Available In most countries today the removal of ammonium ions from drinking water has become almost a necessity. The natural zeolite clinoptiloliteis mined commercially in many parts of the world. It is a selective exchanger for the ammonium cation, and this has prompted its use in water treatment, wastewater treatment, swimming pools and fish farming. The work described in this paper provides dynamic data on cation exchange processes in clinoptilolite involving the NH4 +, Ca+2 and Mg+2 cations. We used material of natural origin – clinoptilolite from Nižný Hrabovec in Slovakia (particle-size 3–5 mm. The breakthrough capacity was determined by dynamic laboratory investigations, and we investigated the influence of thermal pretreatment of clinoptilolite and the concentration of regenerant solution (2, 5, and 10% NaCl. The concentrations of ammonium ion inputs in the tap water that we used were 10, 5, and 2 mg NH4 + l_1 and down to levels below 0.5 mg NH4 + l_1. The experimental results show that repeated pretreatment sufficiently improves the zeolite’s properties, and the structure of clinoptilolite remains unchanged during the loading and regeneration cycles. Ammonium removal capacities were increased by approximately 40 % and 20 % for heat-treated zeolite samples. There was no difference between the regenerates for 10% and 5% NaCl. We conclude that the use of zeolite is an attractive and promising method for ammonium removal.

  19. Aluminum-Based Water Treatment Residue Reuse for Phosphorus Removal

    Lai Yoke Lee

    2015-04-01

    Full Text Available Aluminum-based water treatment residue (Al-WTR generated during the drinking water treatment process is a readily available recycled material with high phosphorus (P adsorption capacity. The P adsorption capacity of Al-WTR generated from Singapore’s water treatment plant was evaluated with reference to particle size range, adsorption pH and temperature. Column tests, with WTR amendments in sand with and without compost, were used to simulate the bioretention systems. The adsorption rate decreased with increasing WTR sizes. Highest P adsorption capacity, 15.57 mg PO43−-P/g WTR, was achieved using fine WTR particles (>50% particles at less than 0.30 mm. At pH 4, the contact time required to reduce effluent P concentration to below the detectable range was half compared with pH 7 and 9. The adsorption rate observed at 40 ± 2 °C was 21% higher compared with that at 30 ± 2 °C. Soil mixes amended with 10% WTR and compost were able to maintain consistently high (90% total phosphorus (TP removal efficiency at a TP load up to 6.45 g/m3. In contrast, TP removal efficiencies associated with columns without WTR amendment decreased to less than 45% as the TP load increased beyond 4.5 g/m3. The results showed that WTR application is beneficial for enhanced TP removal in bioretention systems.

  20. Use of polymeric resins for removing contaminants from oily waters

    Clarisse, M.D.; Queiros, Y.G.C.; Mauro, A.C.; Lucas, E.F. [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Inst. de Macromoleculas; Barbosa, C.C.R. [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil); Barbosa, L.C.F.; Louvisse, A.M.T. [PETROBRAS, Rio de Janeiro, RJ (Brazil). Centro de Pesquisas (CENPES)

    2004-07-01

    Polymeric resins are being tried as an alternative material for treating oily waters from the petroleum industry, which have already been treated by conventional methods. The objective of this work has been to evaluate the purification degree of synthetic oily waters when treated in fixed bed columns packed with polymeric resins made up of hydrophilic and lipophilic moieties. The analysis used for characterizing the total grease and oil content (TOG) was fluorimetry. Starting oily waters of average TOG 40 ppm were prepared. Data obtained from eluted waters did not outweigh 1% of the TOG values of starting solutions. The kinetic study showed that the contaminant removal efficiency depends on the system elution flow rate; optimum removal values were reached at a 7.0 mL/min flow rate. High efficiency and speed in the purification process were obtained at this optimum flow rate. The passage of a water volume 1,000 times the volume of the column bed was not sufficient to observe its saturation level. (author)

  1. Density, distribution, and orientation of water molecules inside and outside carbon nanotubes.

    Thomas, J A; McGaughey, A J H

    2008-02-28

    The behavior of water molecules inside and outside 1.1, 2.8, 6.9, and 10.4 nm diameter armchair carbon nanotubes (CNTs) is predicted using molecular dynamics simulations. The effects of CNT diameter on mass density, molecular distribution, and molecular orientation are identified for both the confined and unconfined fluids. Within 1 nm of the CNT surface, unconfined water molecules assume a spatially varying density profile. The molecules distribute nonuniformly around the carbon surface and have preferred orientations. The behavior of the unconfined water molecules is invariant with CNT diameter. The behavior of the confined water, however, can be correlated to tube diameter. Inside the 10.4 nm CNT, the molecular behavior is indistinguishable from that of the unconfined fluid. Within the smaller CNTs, surface curvature effects reduce the equilibrium water density and force water molecules away from the surface. This effect changes both the molecular distribution and preferred molecular orientations.

  2. Arsenic removal from water using iron-coated seaweeds.

    Vieira, Bárbara R C; Pintor, Ariana M A; Boaventura, Rui A R; Botelho, Cidália M S; Santos, Sílvia C R

    2017-05-01

    Arsenic is a semi-metal element that can enter in water bodies and drinking water supplies from natural deposits and from mining, industrial and agricultural practices. The aim of the present work was to propose an alternative process for removing As from water, based on adsorption on a brown seaweed (Sargassum muticum), after a simple and inexpensive treatment: coating with iron-oxy (hydroxides). Adsorption equilibrium and kinetics were studied and modeled in terms of As oxidation state (III and V), pH and initial adsorbate concentration. Maximum adsorption capacities of 4.2 mg/g and 7.3 mg/g were obtained at pH 7 and 20 °C for arsenite and arsenate, respectively. When arsenite was used as adsorbate, experimental evidences pointed to the occurrence of redox reactions involving As(III) oxidation to As(V) and Fe(III) reduction to Fe(II), with As(V) uptake by the adsorbent. The proposed adsorption mechanism was then based on the assumption that arsenate was the adsorbed arsenic species. The most relevant drawback found in the present work was the considerable leaching of iron to the solution. Arsenite removal from a mining-influenced water by adsorption plus precipitation was studied and compared to a traditional process of coagulation/flocculation. Both kinds of treatment provided practically 100% of arsenite removal from the contaminated water, leading at best in 12.9 μg/L As after the adsorption and precipitation assays and 14.2 μg/L after the coagulation/flocculation process. Copyright © 2017 Elsevier Ltd. All rights reserved.

  3. Pore diffusion limits removal of monochloramine in treatment of swimming pool water using granular activated carbon.

    Skibinski, Bertram; Götze, Christoph; Worch, Eckhard; Uhl, Wolfgang

    2018-04-01

    Overall apparent reaction rates for the removal of monochloramine (MCA) in granular activated carbon (GAC) beds were determined using a fixed-bed reactor system and under conditions typical for swimming pool water treatment. Reaction rates dropped and quasi-stationary conditions were reached quickly. Diffusional mass transport in the pores was shown to be limiting the overall reaction rate. This was reflected consistently in the Thiele modulus, in the effect of temperature, pore size distribution and of grain size on the reaction rates. Pores <2.5 times the diameter of the monochloramine molecule were shown to be barely accessible for the monochloramine conversion reaction. GACs with a significant proportion of large mesopores were found to have the highest overall reactivity for monochloramine removal. Copyright © 2017 Elsevier Ltd. All rights reserved.

  4. Drugs in Your Drinking Water: Removing Pharmaceutical Pollution

    Richardson, K.

    2017-12-01

    Pharmaceuticals, mostly estrogen-based hormones and antibiotics, are increasingly polluting waterways and contaminating municipal drinking water sources. A 2008 study funded by the American Water Works Association Research Foundation and the WateReuse Foundation tested 19 drinking water treatment plants across the United States. The study found pharmaceuticals and metabolites at all of the locations tested. These plants provide drinking water for over 28 million Americans - yet only five states test for pharmaceuticals. A 2007 US Government Accountability Office study of male smallmouth bass showed ovarian tissue in their gonads and concluded the combination of EDCs (Endocrine Disrupting Chemicals) likely caused the feminization of the male fish. The purpose of this project is to determine whether bivalves can effectively remove pharmaceuticals as well as other CECs (Contaminants of Emerging Concern).Pharmaceuticals, specifically ibuprofen, were found to be resistant to chemical and mechanical filtration methods, such as coffee grounds and activated carbon, so biological filtration methods are used. Three types of common mollusks (Sphaeriidae `fingernail clams', freshwater mussels, scallops) will be used to assess the potential for biological remediation of the chemical pollutants. Fifteen specimens of each species will be used - a total of 45 individuals. Each group of five will be introduced to either an NSAID (ibuprofen), oil (vegetable) or hormone (estrogen, pending approval). This creates an array of 3 species and 3 contaminants, for a 3x3 grid of nine sample groups. Water is contaminated with pollutant levels similar to EPA measurements. The concentration will be measured before and after the introduction of the specimens using a UV spectrophotometer, at regular time intervals. As mollusks are capable of filtering up to two liters of water a day, the 37.8 liter tanks are filtered at a rate of 10 liters a day. A successful trial of bivalves reducing and

  5. PAMAM dendrimers and graphene: materials for removing aromatic contaminants from water.

    DeFever, Ryan S; Geitner, Nicholas K; Bhattacharya, Priyanka; Ding, Feng; Ke, Pu Chun; Sarupria, Sapna

    2015-04-07

    We present results from experiments and atomistic molecular dynamics simulations on the remediation of naphthalene by polyamidoamine (PAMAM) dendrimers and graphene oxide (GrO). Specifically, we investigate 3rd-6th generation (G3-G6) PAMAM dendrimers and GrO with different levels of oxidation. The work is motivated by the potential applications of these emerging nanomaterials in removing polycyclic aromatic hydrocarbon contaminants from water. Our experimental results indicate that GrO outperforms dendrimers in removing naphthalene from water. Molecular dynamics simulations suggest that the prominent factors driving naphthalene association to these seemingly disparate materials are similar. Interestingly, we find that cooperative interactions between the naphthalene molecules play a significant role in enhancing their association to the dendrimers and GrO. Our findings highlight that while selection of appropriate materials is important, the interactions between the contaminants themselves can also be important in governing the effectiveness of a given material. The combined use of experiments and molecular dynamics simulations allows us to comment on the possible factors resulting in better performance of GrO in removing polyaromatic contaminants from water.

  6. Iron coated pottery granules for arsenic removal from drinking water.

    Dong, Liangjie; Zinin, Pavel V; Cowen, James P; Ming, Li Chung

    2009-09-15

    A new media, iron coated pottery granules (ICPG) has been developed for As removal from drinking water. ICPG is a solid phase media that produces a stable Fe-Si surface complex for arsenic adsorption. Scanning electron microscopy (SEM) was used to document the physical attributes (grain size, pore size and distribution, surface roughness) of the ICPG media. Several advantages of the ICPG media such as (a) its granular structure, (b) its ability to absorb As via the F(0) coating on the granules' surface; (c) the inexpensive preparation process for the media from clay material make ICPG media a highly effective media for removing arsenic at normal pH. A column filtration test demonstrated that within the stability region (flow rate lower than 15L/h, EBCT >3 min), the concentration of As in the influent was always lower than 50 microg/L. The 2-week system ability test showed that the media consistently removed arsenic from test water to below the 5 microg/L level. The average removal efficiencies for total arsenic, As(III), and As(V) for a 2-week test period were 98%, 97%, and 99%, respectively, at an average flow rate of 4.1L/h and normal pH. Measurements of the Freundlich and Langmuir isotherms at normal pH show that the Freundlich constants of the ICPG are very close to those of ferric hydroxide, nanoscale zero-valent iron and much higher than those of nanocrystalline titanium dioxide. The parameter 1/n is smaller than 0.55 indicating a favorable adsorption process [K. Hristovski, A. Baumgardner, P. Westerhoff, Selecting metal oxide nanomaterials for arsenic removal in fixed bed columns: from nanopowders to aggregated nanoparticle media, J. Hazard. Mater. 147 (2007) 265-274]. The maximum adsorption capacity (q(e)) of the ICPG from the Langmuir isotherm is very close to that of nanoscale zero-valent indicating that zero-valent iron is involved in the process of the As removal from the water. The results of the toxicity characteristic leaching procedure (TCLP

  7. Iron coated pottery granules for arsenic removal from drinking water

    Dong Liangjie; Zinin, Pavel V.; Cowen, James P.; Ming, Li Chung

    2009-01-01

    A new media, iron coated pottery granules (ICPG) has been developed for As removal from drinking water. ICPG is a solid phase media that produces a stable Fe-Si surface complex for arsenic adsorption. Scanning electron microscopy (SEM) was used to document the physical attributes (grain size, pore size and distribution, surface roughness) of the ICPG media. Several advantages of the ICPG media such as (a) its granular structure, (b) its ability to absorb As via the F(0) coating on the granules' surface; (c) the inexpensive preparation process for the media from clay material make ICPG media a highly effective media for removing arsenic at normal pH. A column filtration test demonstrated that within the stability region (flow rate lower than 15 L/h, EBCT >3 min), the concentration of As in the influent was always lower than 50 μg/L. The 2-week system ability test showed that the media consistently removed arsenic from test water to below the 5 μg/L level. The average removal efficiencies for total arsenic, As(III), and As(V) for a 2-week test period were 98%, 97%, and 99%, respectively, at an average flow rate of 4.1 L/h and normal pH. Measurements of the Freundlich and Langmuir isotherms at normal pH show that the Freundlich constants of the ICPG are very close to those of ferric hydroxide, nanoscale zero-valent iron and much higher than those of nanocrystalline titanium dioxide. The parameter 1/n is smaller than 0.55 indicating a favorable adsorption process [K. Hristovski, A. Baumgardner, P. Westerhoff, Selecting metal oxide nanomaterials for arsenic removal in fixed bed columns: from nanopowders to aggregated nanoparticle media, J. Hazard. Mater. 147 (2007) 265-274]. The maximum adsorption capacity (q e ) of the ICPG from the Langmuir isotherm is very close to that of nanoscale zero-valent indicating that zero-valent iron is involved in the process of the As removal from the water. The results of the toxicity characteristic leaching procedure (TCLP) analysis

  8. Water hyacinths and alligator weeds for removal of silver, cobalt, and strontium from polluted waters

    Wolverton, B. C.; Mcdonald, R. C.

    1975-01-01

    Water hyacinths and alligator weeds demonstrated the ability to rapidly remove heavy metals from an aqueous system by root absorption and concentration. Water hyacinths demonstrated the ability to remove 0.439 mg of silver, 0.568 mg of cobalt, and 0.544 mg of strontium in an ionized form per gram of dry plant material in a 24-hour period. Alligator weeds removed a maximum of 0.439 mg of silver, 0.130 mg of cobalt, and 0.161 mg of strontium per gram of dry plant material per day.

  9. Diclofenac removal from water with ozone and activated carbon.

    Beltrán, Fernando J; Pocostales, Pablo; Alvarez, Pedro; Oropesa, Ana

    2009-04-30

    Diclofenac (DCF) has been treated in water with ozone in the presence of various activated carbons. Activated carbon-free ozonation or single ozonation leads to a complete degradation of DCF in less than 15 min while in the presence of activated carbons higher degradation rates of TOC and DCF are noticeably achieved. Among the activated carbons used, P110 Hydraffin was found the most suitable for the catalytic ozonation of DCF. The influence of pH was also investigated. In the case of the single ozonation the increasing pH slightly increases the TOC removal rate. This effect, however, was not so clear in the presence of activated carbons where the influence of the adsorption process must be considered. Ecotoxicity experiments were performed, pointing out that single ozonation reduces the toxicity of the contaminated water but catalytic ozonation improved those results. As far as kinetics is concerned, DCF is removed with ozone in a fast kinetic regime and activated carbon merely acts as a simple adsorbent. However, for TOC removal the ozonation kinetic regime becomes slow. In the absence of the adsorbent, the apparent rate constant of the mineralization process was determined at different pH values. On the other hand, determination of the rate constant of the catalytic reaction over the activated carbon was not possible due to the effect of mass transfer resistances that controlled the process rate at the conditions investigated.

  10. Removal of emerging micropollutants from water using cyclodextrin.

    Nagy, Zsuzsanna Magdolna; Molnár, Mónika; Fekete-Kertész, Ildikó; Molnár-Perl, Ibolya; Fenyvesi, Éva; Gruiz, Katalin

    2014-07-01

    Small scale laboratory experiment series were performed to study the suitability of a cyclodextrin-based sorbent (ß-cyclodextrin bead polymer, BCDP) for modelling the removal of micropollutants from drinking water and purified waste water using simulated inflow test solutions containing target analytes (ibuprofen, naproxen, ketoprofen, bisphenol-A, diclofenac, β-estradiol, ethinylestradiol, estriol, cholesterol at 2-6 μg/L level). This work was focused on the preliminary evaluation of BCDP as a sorbent in two different model systems (filtration and fluidization) applied for risk reduction of emerging micropollutants. For comparison different filter systems combined with various sorbents (commercial filter and activated carbon) were applied and evaluated in the filtration experiment series. The spiked test solution (inflow) and the treated outflows were characterized by an integrated methodology including chemical analytical methods gas chromatography-tandem mass spectrometry (GC-MS/MS) and various environmental toxicity tests to determine the efficiency and selectivity of the applied sorbents. Under experimental conditions the cyclodextrin-based filters used for purification of drinking water in most cases were able to absorb more than 90% of the bisphenol-A and of the estrogenic compounds. Both the analytical chemistry and toxicity results showed efficient elimination of these pollutants. Especially the toxicity of the filtrate decreased considerably. Laboratory experiment modelling post-purification of waste water was also performed applying fluidization technology by ß-cyclodextrin bead polymer. The BCDP removed efficiently from the spiked test solution most of the micropollutants, especially the bisphenol-A (94%) and the hormones (87-99%) The results confirmed that the BCDP-containing sorbents provide a good solution to water quality problems and they are able to decrease the load and risk posed by micropollutants to the water systems. Copyright © 2014

  11. Point-of-entry removal of radon from drinking water

    Lowry, J.D.; Brutsaert, W.F.; Mc Enerney, T.; Molk, C.

    1987-01-01

    Two processes were investigated in the laboratory to determine their efficiency for removing radon from household water supplies. Granular activated carbon (GAC) adsorption was found to be extremely effective as a result of an adsorption-decay steady state that is established quickly and continues for years. The GAC bed, however, adsorbs radon progeny as the radon decays, and it becomes a source of gamma radiation. This problem is believed to be manageable for the vast majority of potential applications. Diffused bubble aeration was found to be as effective as GAC, with removals of greater than 99 percent being practical. Although more costly than GAC, aeration does not have the problem of gamma activity buildup

  12. Chemical reactions of water molecules on Ru(0001) induced by selective excitation of vibrational modes

    Mugarza, Aitor; Shimizu, Tomoko K.; Ogletree, D. Frank; Salmeron, Miquel

    2009-05-07

    Tunneling electrons in a scanning tunneling microscope were used to excite specific vibrational quantum states of adsorbed water and hydroxyl molecules on a Ru(0 0 0 1) surface. The excited molecules relaxed by transfer of energy to lower energy modes, resulting in diffusion, dissociation, desorption, and surface-tip transfer processes. Diffusion of H{sub 2}O molecules could be induced by excitation of the O-H stretch vibration mode at 445 meV. Isolated molecules required excitation of one single quantum while molecules bonded to a C atom required at least two quanta. Dissociation of single H{sub 2}O molecules into H and OH required electron energies of 1 eV or higher while dissociation of OH required at least 2 eV electrons. In contrast, water molecules forming part of a cluster could be dissociated with electron energies of 0.5 eV.

  13. Influence of orientation averaging on the anisotropy of thermal neutrons scattering on water molecules

    Markovic, M. I.; Radunovic, J. B.

    1976-01-01

    Determination of spatial distribution of neutron flux in water, most frequently used moderator in thermal reactors, demands microscopic scattering kernels dependence on cosine of thermal neutrons scattering angle when solving the Boltzmann equation. Since spatial orientation of water molecules influences this dependence it is necessary to perform orientation averaging or rotation-vibrational intermediate scattering function for water molecules. The calculations described in this paper and the obtained results showed that methods of orientation averaging do not influence the anisotropy of thermal neutrons scattering on water molecules, but do influence the inelastic scattering

  14. Removal of Arsenic from Drinking Water Using Modified Activated Alumina

    Mohammad Mosaferi

    2005-09-01

    Full Text Available Considering contamination of drinking water to arsenic in some villages ofIran. In order to develop a simple method for household water treatment in rural areas, efficiency of  modified activated alumina with iron compounds- a product of Alcan Company with trade name of AAFS-50- was studied Equilibrium batch experiments were carried out using shaker incubator and arsenic was analyzed with SDDC method. Effects of initial concentration of arsenic, adsorbent dose, oxidation state of arsenic, pH and oxidation with chlorine on adsorption were studied. Correlation coefficient of Freundlich and Laungmuier  isotherms  for As(V and As(III were 0.964 , 0.991 and 0.970, 0.978 respectively . These results show that adsorption of arsenic on modified activated alumina is compatible with both models specially Laungmuier models. Removal efficiency of As(V at 0.5 ,1 and 2 hr increased with doubling the adsorbent dose from 44.8 to 72%, 69.6 to 90.8 and 92.4 to 98% ; respectively. Experiments using different concentrations of arsenic showed that adsorption of arsenic on activated alumina are a first order reaction that is, rate of reaction is dependent on intial; concentration of arsenic. Removal efficiency for concentration of 0.250 mg/L of arsenic, with increasing of reaction time from 15 min to 60 min, increased 1.54 times and reached from 61% to 94%. During 2hrs, removal of As(V and As(III were 96% and 16% respectively. Using 1.5 mg/L Chlorine as oxidant agent, removal of As(III was increased to 94%. In the case of pH effect, rate of adsorption increased for arsenite, with increasing of pH to 8 and decreased with more increasing, so that adsorption at pH 14 was equal to pH 2. For arsenate, the most adsorption was observed at pH between 6 to 8 . These results show that by using the studied activated alumina, there will not be need for adjustment of pH and the activated alumina used in this study could have application as a safe adsorbent for removal of

  15. REMOVING AGGRESSIVE CARBON DIOXIDE FROM WATER USING MELAPHYRE BED

    Magdalena Maria Michel

    2017-09-01

    Full Text Available The experiment was based on filtration of the highly aggressive water through the melaphyre bed. The quartz bed was non-reactive reference material. The aim of this work was to determine the ability of the melaphyre to remove aggressive CO2 during the chemical reaction. It was noted that a decrease of acidity of the filtrate in comparison to the feed and an increase of its alkalinity and pH. It was calculated that until the moment of exhaustion of the de-acidifying properties of the melaphyre, maximum amount of bound CO2 added to the water was 29.7 g CO2/L of the bed, and maximum amount of the aggressive CO2 removed from the water was 33.3 g CO2/L of the bed. Regarding very high content of the aggressive CO2 (116 mg/L average in the feed only 28.76% of this component was subject to transformation into bound and affiliated CO2 in the filtrate. For the melaphyre bed the CO2 loss from the experiment system following from desorption was 7.80% of the total load of CO2 added with the feed. On the quartz bed the loss was slightly lower 4.56%.

  16. REMOVAL OF ARSENIC IN DRINKING WATER: ARS CFU-50 APC ELECTROFLOCCULATION AND FILTRATION WATER TREATMENT SYSTEM

    ETV testing of the ARS CFU-50 APC Electroflocculation and Filtration Water Treatment System (ARS CFU-50 APC) for arsenic removal was conducted at the Town of Bernalillo Well #3 site from April 18 through May 2, 2006. The source water was chlorinated groundwater from two supply w...

  17. The mechanism of 2-dimensional manipulation of DNA molecules by water and ethanol flows

    Shen Zigang; Huang Yibo; Li Bin; Zhang Yi

    2007-01-01

    Due to its unique physical and chemical properties, DNA has recently become a promising material for building blocks in nanofabrication. Many researches focus on how to use DNA molecules as a template for nanowires. Molecular Combing technique is one of important methods to manipulate DNA molecules by using a water meniscus and form specific DNA nano-structures on surfaces. In this paper, by employing a modified molecular combing technique, special patterns of DNA molecules was formed, and the interaction between liquid flows or meniscus and DNA molecules was analyzed, and the mechanism of manipulating DNA molecules by liquid was studied. (authors)

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

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

    2011-01-01

    Exposure to arsenic through drinking water poses a threat to human health. Electrocoagulation is a water treatment technology that involves electrolytic oxidation of anode materials and in-situ generation of coagulant. The electrochemical generation of coagulant is an alternative to using chemical coagulants, and the process can also oxidize As(III) to As(V). Batch electrocoagulation experiments were performed in the laboratory using iron electrodes. The experiments quantified the effects of pH, initial arsenic concentration and oxidation state, and concentrations of dissolved phosphate, silica and sulfate on the rate and extent of arsenic removal. The iron generated during electrocoagulation precipitated as lepidocrocite (γ-FeOOH), except when dissolved silica was present, and arsenic was removed by adsorption to the lepidocrocite. Arsenic removal was slower at higher pH. When solutions initially contained As(III), a portion of the As(III) was oxidized to As(V) during electrocoagulation. As(V) removal was faster than As(III) removal. The presence of 1 and 4 mg/L phosphate inhibited arsenic removal, while the presence of 5 and 20 mg/L silica or 10 and 50 mg/L sulfate had no significant effect on arsenic removal. For most conditions examined in this study, over 99.9% arsenic removal efficiency was achieved. Electrocoagulation was also highly effective at removing arsenic from drinking water in field trials conducted in a village in Eastern India. By using operation times long enough to produce sufficient iron oxide for removal of both phosphate and arsenate, the performance of the systems in field trials was not inhibited by high phosphate concentrations. Copyright © 2010 Elsevier Ltd. All rights reserved.

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

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

    2010-02-01

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

  20. Community Responses to the Removal of Bottled Water on a University Campus

    Mikhailovich, Katja; Fitzgerald, Robert

    2014-01-01

    Purpose: This paper aimed to examine the impact of the removal of bottled water on the campus community. This paper presents the findings of a survey conducted at the first Australian university to remove single-use bottled water from sale on a small regional university campus. The removal of bottled water from sale at the university formed part…

  1. Removal of fluoride from water using aluminium containing compounds

    M. Karthikeyan; K. P. Elango

    2009-01-01

    Batch adsorption studies were undertaken to assess the suitability of aluminium titanate (AT) and bismuth aluminate (BA) to remove fluoride ions from water.The effect of pH,dose of adsorbent,contact time,initial concentration,co-ions and temperature on fluoride removal efficiency were studied.The amounts of fluoride ions adsorbed,at 30℃ from 4 mg/L of fluoride ion solution,by AT and BA are 0.85 and 1.55 mg/g,respectively.The experimental data fitted well to the Freundlich and Langmuir isotherms.Thermodynamic parameters such as △H~0,△S~0 and △G~0 indicated that the removal of fluoride ions by AT is exothermic and non-spontaneous while that by BA is endothermic and spontaneous.Furrier transform infrared (FT-IR) analysis and X-ray diffraction (XRD) patterns of the adsorbent before and after adsorption indicated that fluoride ions are chemisorbed by these adsorbents.

  2. Removal of Foodborne Pathogen Biofilms by Acidic Electrolyzed Water

    Qiao Han

    2017-06-01

    Full Text Available Biofilms, which are complex microbial communities embedded in the protective extracellular polymeric substances (EPS, are difficult to remove in food production facilities. In this study, the use of acidic electrolyzed water (AEW to remove foodborne pathogen biofilms was evaluated. We used a green fluorescent protein-tagged Escherichia coli for monitoring the efficiency of AEW for removing biofilms, where under the optimal treatment conditions, the fluorescent signal of cells in the biofilm disappeared rapidly and the population of biofilm cells was reduced by more than 67%. Additionally, AEW triggered EPS disruption, as indicated by the deformation of the carbohydrate C-O-C bond and deformation of the aromatic rings in the amino acids tyrosine and phenylalanine. These deformations were identified by EPS chemical analysis and Raman spectroscopic analysis. Scanning electron microscopy (SEM images confirmed that the breakup and detachment of biofilm were enhanced after AEW treatment. Further, AEW also eradicated biofilms formed by both Gram-negative bacteria (Vibrio parahaemolyticus and Gram-positive bacteria (Listeria monocytogenes and was observed to inactivate the detached cells which are a potential source of secondary pollution. This study demonstrates that AEW could be a reliable foodborne pathogen biofilm disrupter and an eco-friendly alternative to sanitizers traditionally used in the food industry.

  3. A biosystem for removal of metal ions from water

    Kilbane, J.J. II.

    1990-01-01

    The presence of heavy metal ions in ground and surface waters constitutes a potential health risk and is an environmental concern. Moreover, processes for the recovery of valuable metal ions are of interest. Bioaccumulation or biosorption is not only a factor in assessing the environmental risk posed by metal ions; it can also be used as a means of decontamination. A biological system for the removal and recovery of metal ions from contaminated water is reported here. Exopolysaccharide-producing microorganisms, including a methanotrophic culture, are demonstrated to have superior metal binding ability, compared with other microbial cultures. This paper describes a biosorption process in which dried biomass obtained from exopolysaccharide-producing microorganisms is encapsulated in porous plastic beads and is used for metal ion binding and recovery. 22 refs., 13 figs.

  4. Removal of chlorinated ethylenes from drinking water by radiation treatments

    Gehringer, P.; Proksch, E.; Eschweiler, H.; Szinovatz, W.

    1990-01-01

    Per- and trichloroethylene dissolved in sub-ppm amounts in Vienna City drinking water are decomposed under γ-irradiations according to first-order rate laws. Doses D 90 necessary for a 90% pollutant removal are 255 Gy (perchloroethylene) and 120 Gy (trichloroethylene). For other waters D 90 values increase with increasing concentration of organic and inorganic solutes present, especially of bicarbonate. Main decomposition products are Cl - , CO 2 and (for trichloroethylene only) HCOOH. The additional presence of 0.5 to 10 ppm ozone decreases the D 90 values by factors up to ten; they can be as low as 33 Gy (perchloroethylene) or even 12 Gy (trichloroethylene). The rate laws, however, are no longer of first, but of higher order. (author)

  5. Removal of actinides from dilute waste waters using polymer filtration

    Smith, B.F.; Robison, T.W.; Gibson, R.R.

    1995-01-01

    More stringent US Department of Energy discharge regulations for waste waters containing radionuclides (30 pCi/L total alpha) require the development of new processes to meet the new discharge limits for actinide metal ions, particularly americium and plutonium, while minimizing waste. We have been investigating a new technology, polymer filtration, that has the potential for effectively meeting these new limits. Traditional technology uses basic iron precipitation which produces large amounts of waste sludge. The new technology is based on using water-soluble chelating polymers with ultrafiltration for physical separation. The actinide metal ions are selectively bound to the polymer and can not pass through the membrane. Small molecules and nonbinding metals pass through the membrane. Advantages of polymer filtration technology compared to ion, exchange include rapid kinetics because the binding is occurring in a homogenous solution and no mechanical strength requirement on the polymer. We will present our results on the systematic development of a new class of water-soluble chelating polymers and their binding ability from dilute acid to near neutral waters

  6. Removing NDMA (N,N-dimethylnitrosamine) from natural waters

    Mezyk, S.P.; Cooper, W.J.; Bartels, D.M.

    2003-01-01

    Nitrosoamines are ubiquitous in water environments, and are of concern as they are potent carcinogens. In particular, N,N-dimethylnitrosamine (NDMA, (CH 3 ) 2 NNO) is volatile, and therefore has been detected around factories producing secondary amines or rocket fuel, in areas near industrial plants that use dimethylamine in organic synthesis, and even in foods and beverages that contain nitrite or which have been exposed to nitrous oxides. Various technologies have been suggested for removing trace levels of NDMA contamination from aqueous systems. However, Advanced Oxidation Technologies (AOTs), such as ozone, UV/ozone, and UV/H 2 O 2 , which use oxidation via the hydroxyl radical ( . OH), or heterogeneous catalysis by TiO 2 , sonolysis, or the electron beam process, which produce a mixture of oxidizing . OH radicals with reducing hydrated electrons (e - aq ) and hydrogen atoms ( . H), may also produce unwanted stable products in the treatment. Some of these stable products, such as secondary amines, allow regeneration of NDMA to occur. To ensure that any process applied to NDMA contaminated water occurs efficiently and quantitatively a complete understanding of the chemistry involved under the conditions of use is necessary. This requires mathematical modeling of the process, which in turn needs reaction rate constants and mechanisms. In this study, absolute rate constants at room temperature for the reaction of the hydroxyl radical, hydrated electron, and hydrogen atom with NDMA in water have been determined using electron pulse radiolysis and absorption spectroscopy, (e - aq and . OH) and EPR free induction decay attenuation ( . H) measurements. The specific values of (4.30± 0.12) x 10 8 , (1.41 ± 0.02) x 10 10 , and (2.01 ± 0.03) x 10 8 M -1 s -1 , respectively, demonstrate that the reductive destruction of this nitrosoamine would be the dominant removal pathway in any remediation process. Based on these data we have begun modeling the large-scale electron

  7. Iron oxide hydroxide nanoflower assisted removal of arsenic from water

    Raul, Prasanta Kumar, E-mail: prasanta.drdo@gmail.com [Defence Research Laboratory, Post Bag No. 2, Tezpur 784001, Assam (India); Devi, Rashmi Rekha; Umlong, Iohborlang M. [Defence Research Laboratory, Post Bag No. 2, Tezpur 784001, Assam (India); Thakur, Ashim Jyoti [Department of Chemical Sciences, Tezpur University, Napaam, Tezpur 784028, Assam (India); Banerjee, Saumen; Veer, Vijay [Defence Research Laboratory, Post Bag No. 2, Tezpur 784001, Assam (India)

    2014-01-01

    Graphical abstract: Non-magnetic polycrystalline iron oxide hydroxide nanoparticle with flower like morphology is found to play as an effective adsorbent media to remove As(III) from 300 μg L{sup −1} to less than 10 μg L{sup −1} from drinking water over wide range of pH. TEM image clearly reveals that the nanoparticle looks flower like morphology with average particle size less than 20 nm. The maximum sorption capacity of the sorbent is found to be 475 μg g{sup −1} for arsenic at room temperature and the data fitted to different isotherm models indicate the heterogeneity of the adsorbent surface. The material can be regenerated up to 70% using dilute hydrochloric acid and it would be utilized for de-arsenification purposes. - Highlights: • The work includes synthesis of iron oxide hydroxide nanoflower and its applicability for the removal of arsenic from water. • The nanoparticle was characterized using modern instrumental methods like FESEM, TEM, BET, XRD, etc. • The maximum sorption capacity of the sorbent is found to be 475 μg g{sup −1} for arsenic at room temperature. • The sorption is multilayered on the heterogeneous surface of the nano adsorbent. • The mechanism of arsenic removal of IOH nanoflower follows both adsorption and ion-exchange. - Abstract: Non-magnetic polycrystalline iron oxide hydroxide nanoparticle with flower like morphology is found to play as an effective adsorbent media to remove As(III) from 300 μg L{sup −1} to less than 10 μg L{sup −1} from drinking water over wide range of pH. The nanoparticle was characterized by X-ray powder diffraction analysis (XRD), BET surface area, FTIR, FESEM and TEM images. TEM image clearly reveals flower like morphology with average particle size less than 20 nm. The nanoflower morphology is also supported by FESEM images. The maximum sorption capacity of the sorbent is found to be 475 μg g{sup −1} for arsenic and the data fitted to different isotherm models indicate the

  8. Removal of toxic chemicals from water with activated carbon

    Dawson, V.K.; Marking, L.L.; Bills, T.D.

    1976-01-01

    Activated carbon was effective in removing fish toxicants and anesthetics from water solutions. Its capacity to adsorb 3-trifluoromethyl-4-nitrophenol (TFM), antimycin, NoxfishA? (5% rotenone), Dibrorms, juglone, MSa??222, and benzocaine ranged from 0.1 to 64 mg per gram of carbon. The adsorptive capacity (end point considered as a significant discharge) of activated carbon for removal of TFM was determined at column depths of 15, 30, and 60 cm; temperatures of 7, 12, 17, and 22 C; pH's of 6.5, 7.5, 8.5, and 9.5; and flow rates of 50, 78, 100, 200, and 940 ml/min. Adsorptive capacity increased when the contact time was increased by reducing the flow rate or increasing the column depth. The adsorptive capacity was not significantly influenced by temperature but was substantially higher at pH 6.5 than at the other pH's tested. A practical and efficient filter for purifying chemically treated water was developed.

  9. Removal of Metal Nanoparticles Colloidal Solutions by Water Plants

    Olkhovych, Olga; Svietlova, Nataliia; Konotop, Yevheniia; Karaushu, Olena; Hrechishkina, Svitlana

    2016-11-01

    The ability of seven species of aquatic plants ( Elodea canadensis, Najas guadelupensis, Vallisneria spiralis L., Riccia fluitans L., Limnobium laevigatum, Pistia stratiotes L., and Salvinia natans L.) to absorb metal nanoparticles from colloidal solutions was studied. It was established that investigated aquatic plants have a high capacity for removal of metal nanoparticles from aqueous solution (30-100%) which indicates their high phytoremediation potential. Analysis of the water samples content for elements including the mixture of colloidal solutions of metal nanoparticles (Mn, Cu, Zn, Ag + Ag2O) before and after exposure to plants showed no significant differences when using submerged or free-floating hydrophytes so-called pleuston. However, it was found that the presence of submerged hydrophytes in aqueous medium ( E. canadensis, N. guadelupensis, V. spiralis L., and R. fluitans L.) and significant changes in the content of photosynthetic pigments, unlike free-floating hydrophytes ( L. laevigatum, P. stratiotes L., S. natans L.), had occur. Pleuston possesses higher potential for phytoremediation of contaminated water basins polluted by metal nanoparticles. In terms of removal of nanoparticles among studied free-floating hydrophytes, P. stratiotes L. and S. natans L. deserve on special attention.

  10. Inorganic arsenic removal in rice bran by percolating cooking water.

    Signes-Pastor, Antonio J; Carey, Manus; Meharg, Andrew A

    2017-11-01

    Rice bran, a by-product of milling rice, is highly nutritious but contains very high levels of the non-threshold carcinogen inorganic arsenic (i-As), at concentrations around 1mg/kg. This i-As content needs to be reduced to make rice bran a useful food ingredient. Evaluated here is a novel approach to minimizing rice bran i-As content which is also suitable for its stabilization namely, cooking bran in percolating arsenic-free boiling water. Up to 96% of i-As removal was observed for a range of rice bran products, with i-As removal related to the volume of cooking water used. This process reduced the copper, potassium, and phosphorus content, but had little effect on other trace- and macro-nutrient elements in the rice bran. There was little change in organic composition, as assayed by NIR, except for a decrease in the soluble sugar and an increase, due to biomass loss, in dietary fiber. Copyright © 2017 Elsevier Ltd. All rights reserved.

  11. APPLICATION OF POWDERY ACTIVATED CARBONS FOR REMOVAL IBUPROFEN FROM WATER

    Alicja Puszkarewicz

    2017-07-01

    Full Text Available The paper presents results of studies on the use of adsorptive properties of selected powdered activated carbons (Norit SA Super and Carbopol MB5 for removal of ibuprofen from water. The tests were performed on non-flow conditions, series depending on the type and dose of powdered adsorbents. The research was carried out on a model solution of ibuprofen at initial concentration C0 = 20 mg/dm3, at 200 C. Froundlich and Langmuir adsorption isotherms were used. Lagergrene kinetic models (PFO and Ho (PSO were used to describe adsorption kinetics. Both carbons exhibited a higher affinity for the adsorbent at a pH above 7. The better adsorbent was the Norit SA Super, for which, the highest adsorption capacity q = 0.448 g/g was achieved with dose D = 35 mg/dm3. The effectiveness of adsorption (decrease of ibuprofen in water was 78%. Total removal of ibuprofen was obtained for a dose of carbon D = 200 mg/dm3. With respect to Carbopol, the highest adsorption capacity (q = 0.353 g / g was achieved at a dose of 30 mg / dm3, resulting in a 53% efficiency. Studies have shown that both tested powdered activated carbons have contributed to effective cleaning of aqueous solutions containing ibuprofen.

  12. ETV REPORT: REMOVAL OF ARSENIC IN DRINKING WATER ORCA WATER TECHNOLOGIES KEMLOOP 1000 COAGULATION AND FILTRATION WATER TREATMENT SYSTEM

    Verification testing of the ORCA Water Technologies KemLoop 1000 Coagulation and Filtration Water Treatment System for arsenic removal was conducted at the St. Louis Center located in Washtenaw County, Michigan, from March 23 through April 6, 2005. The source water was groundwate...

  13. Sorptive removal of tetracycline from water by palygorskite

    Chang, Po-Hsiang; Li, Zhaohui; Yu, Tsai-Luen; Munkhbayer, Sandagdori; Kuo, Tzu-Hsing; Hung, Yu-Chiao; Jean, Jiin-Shuh; Lin, Kao-Hung

    2009-01-01

    Extensive use of pharmaceuticals and growth hormone in farm animal and live stocks has resulted in their frequent detection in soils, groundwater, and wastewater. The fate and transport of these compounds are strongly affected by their sorptive behavior to the soil minerals and humic materials. In this research, we conducted the sorption of tetracycline (TC), a common antibiotic, on palygorskite (PFL-1), a fibrous clay mineral of high surface area and high sorptivity towards organic compounds. The results showed that the sorption capacity of TC on PFL-1 was as high as 210 mmol/kg at pH 8.7. The sorption was relatively fast and reached equilibrium in 2 h. Solution pH and ionic strength had significant effects on TC sorption. The sorption of TC by palygorskite is endothermic and the free energy of sorption is in the range of -10 to -30 kJ/mol, suggesting a strong physical sorption. The X-ray diffraction patterns before and after TC sorption revealed no changes in d-spacing and intensity under different pH and initial TC concentrations, indicating that the sorbed TC molecules are on the external surface of the mineral in contrast to intercalation of TC into swelling clays, such as montmorillonite. The small positive value of entropy change suggested that TC molecules are in disordered arrangement on palygorskite surfaces. Surface sorption of TC on PFL-1 is further supported by the derivative of gravimetric analysis and by the calculation of the amount of TC sorption normalized to the surface area. The results suggest that palygorskite could be a good candidate to remove TC from wastewater containing higher amounts of TC.

  14. Implication of Crystal Water Molecules in Inhibitor Binding at ALR2 Active Site

    Hymavati

    2012-01-01

    Full Text Available Water molecules play a crucial role in mediating the interaction between a ligand and a macromolecule. The solvent environment around such biomolecule controls their structure and plays important role in protein-ligand interactions. An understanding of the nature and role of these water molecules in the active site of a protein could greatly increase the efficiency of rational drug design approaches. We have performed the comparative crystal structure analysis of aldose reductase to understand the role of crystal water in protein-ligand interaction. Molecular dynamics simulation has shown the versatile nature of water molecules in bridge H bonding during interaction. Occupancy and life time of water molecules depend on the type of cocrystallized ligand present in the structure. The information may be useful in rational approach to customize the ligand, and thereby longer occupancy and life time for bridge H-bonding.

  15. Effectiveness of table top water pitcher filters to remove arsenic from drinking water.

    Barnaby, Roxanna; Liefeld, Amanda; Jackson, Brian P; Hampton, Thomas H; Stanton, Bruce A

    2017-10-01

    Arsenic contamination of drinking water is a serious threat to the health of hundreds of millions of people worldwide. In the United States ~3 million individuals drink well water that contains arsenic levels above the Environmental Protection Agency (EPA) maximum contaminant level (MCL) of 10μg/L. Several technologies are available to remove arsenic from well water including anion exchange, adsorptive media and reverse osmosis. In addition, bottled water is an alternative to drinking well water contaminated with arsenic. However, there are several drawbacks associated with these approaches including relatively high cost and, in the case of bottled water, the generation of plastic waste. In this study, we tested the ability of five tabletop water pitcher filters to remove arsenic from drinking water. We report that only one tabletop water pitcher filter tested, ZeroWater®, reduced the arsenic concentration, both As 3+ and As 5+ , from 1000μg/L to water and its use reduces plastic waste associated with bottled water. Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.

  16. Grafted cellulose for PAHs removal present in industrial discharge waters

    Euvrard, Elise; Druart, Coline; Poupeney, Amandine; Crini, Nadia; Vismara, Elena; Lanza, Tommaso; Torri, Giangiacomo; Gavoille, Sophie; Crini, Gregorio

    2014-05-01

    Keywords: cellulose; biosorbent; PAHs; polycontaminated wastewaters; trace levels. Polycyclic aromatic hydrocarbons (PAHs), chemicals essentially formed during incomplete combustion of organic materials from anthropogenic activities, were present in all compartments of the ecosystem, air, water and soil. Notably, a part of PAHs found in aquatic system was introduced through industrial discharge waters. Since the Water Framework Directive has classified certain PAHs as priority hazardous substances, industrials are called to take account this kind of organic pollutants in their global environmental concern. Conventional materials such as activated carbons definitively proved their worth as finishing treatment systems but remained costly. In this study, we proposed to use cellulose grafted with glycidyl methacrylate [1] for the removal of PAHs present in discharge waters of surface treatment industries. Firstly, to develop the device, we worked with synthetic solutions containing 16 PAHs at 500 ng/L. Two types of grafted cellulose were tested over a closed-loop column with a concentration of 4g cellulose/L: cellulose C2 with a hydroxide group and cellulose C4 with an amine group. No PAH was retained by the raw cellulose whereas abatement percentages of PAHs were similar between C2 and C4 (94% and 98%, respectively, for the sum of the 16 PAHs) with an experiment duration of 400 min (corresponding to about 20 cycles through grafted cellulose). Secondly, to determine the shorter time to abate the amount maximum of PAHs through the system, a kinetic was realized from 20 min (one cycle) to 400 min with C4. The steady state (corresponding to about 95% of abatement of the total PAHs) was reached at 160 min. Finally, the system was then tested with real industrial discharge waters containing both mineral and organic compounds. The results indicated that the abatement percentage of PAHs was similar between C2 and C4, corroborating the tests with synthetic solution. In return

  17. Phosphate removal from water using lithium intercalated gibbsite.

    Wang, Shan-Li; Cheng, Chia-Yi; Tzou, Yu-Min; Liaw, Ren-Bao; Chang, Ta-Wei; Chen, Jen-Hshuan

    2007-08-17

    In this study, lithium intercalated gibbsite (LIG) was investigated for its effectiveness at removing phosphate from water and the mechanisms involved. LIG was prepared through intercalating LiCl into gibbsite giving a structure of [LiAl2(OH)6]+ layers with interlayer Cl- and water. The results of batch adsorption experiments showed that the adsorption isotherms at various pHs exhibited an L-shape and could be fitted well using the Langmuir model. The Langmuir adsorption maximum was determined to be 3.0 mmol g(-1) at pH 4.5 and decreased with increasing pH. The adsorption of phosphate was mainly through the displacement of the interlayer Cl- ions in LIG. In conjunction with the anion exchange reaction, the formation of surface complexes or precipitates could also readily occur at lower pH. The adsorption decreased with increasing pH due to decreased H(2)PO(4)(-)/HPO4(2-) molar ratio in solution and positive charges on the edge faces of LIG. Anion exchange is a fast reaction and can be completed within minutes; on the contrary, surface complexation is a slow process and requires days to reach equilibrium. At lower pH, the amount of adsorbed phosphate decreased significantly as the ionic strength was increased from 0.01 to 0.1M. The adsorption at higher pH showed high selectivity toward divalent HPO4(2-) ions with an increase in ionic strength having no considerable effect on the phosphate adsorption. These results suggest that LIG may be an effective scavenger for removal of phosphate from water.

  18. Effects of water removal on a Hawaiian stream ecosystem

    Kinzie, R. A.; Chong, C.; Devrell, J.; Lindstrom, D.; Wolff, R.

    2006-01-01

    A 3-year study of Wainiha River on Kaua'i, Hawai'i, was carried out to determine the impact that water removal had on key stream ecosystem parameters and functions. The study area included a diversion dam for a hydroelectric plant that removes water at an elevation of 213 m and returns it to the stream about 6 km downstream at an elevation of 30 m. There were two high-elevation sites, one with undiverted flow and one with reduced flow, and two low-elevation sites, one with reduced flow and one with full flow restored. Monthly samples were taken of instream and riparian invertebrates and plants. When samples from similar elevations were compared, dewatered sites had lower concentrations of benthic photosynthetic pigments than full-flow sites, and benthic ash-free dry mass (AFDM) was higher at the two low-elevation sites regardless of flow. Benthic chlorophyll a (chl a) and AFDM were higher in summer months than in the winter. Benthic invertebrate abundance was highest at the full-flow, low-elevation site and benthic invertebrate biomass was highest at the full-flow, high-elevation site. Season had only marginal effects on abundance and biomass of benthic invertebrates. Diversity of benthic invertebrates was higher at the more-downstream sites. Abundance of drifting invertebrates was highest at the site above the diversion dam and generally higher in winter than in summer months. Biomass of drifting invertebrates was also highest at the above-dam site but there was little seasonal difference. Almost all parameters measured were lowest at the site just downstream of the diversion dam. The biotic parameters responded only weakly to flows that had occurred up to 1 month before the measurements were made. Flow, elevation, and season interact in complex ways that impact ecosystem parameters and functions, but water diversion can override all these environmental factors. ?? 2006 by University of Hawai'i Press All rights reserved.

  19. Phosphate removal from water using lithium intercalated gibbsite

    Wang, S.-L.; Cheng, C.-Y.; Tzou, Y.-M.; Liaw, R.-B.; Chang, T.-W.; Chen, J.-H.

    2007-01-01

    In this study, lithium intercalated gibbsite (LIG) was investigated for its effectiveness at removing phosphate from water and the mechanisms involved. LIG was prepared through intercalating LiCl into gibbsite giving a structure of [LiAl 2 (OH) 6 ] + layers with interlayer Cl - and water. The results of batch adsorption experiments showed that the adsorption isotherms at various pHs exhibited an L-shape and could be fitted well using the Langmuir model. The Langmuir adsorption maximum was determined to be 3.0 mmol g -1 at pH 4.5 and decreased with increasing pH. The adsorption of phosphate was mainly through the displacement of the interlayer Cl - ions in LIG. In conjunction with the anion exchange reaction, the formation of surface complexes or precipitates could also readily occur at lower pH. The adsorption decreased with increasing pH due to decreased H 2 PO 4 - /HPO 4 2- molar ratio in solution and positive charges on the edge faces of LIG. Anion exchange is a fast reaction and can be completed within minutes; on the contrary, surface complexation is a slow process and requires days to reach equilibrium. At lower pH, the amount of adsorbed phosphate decreased significantly as the ionic strength was increased from 0.01 to 0.1 M. The adsorption at higher pH showed high selectivity toward divalent HPO 4 2- ions with an increase in ionic strength having no considerable effect on the phosphate adsorption. These results suggest that LIG may be an effective scavenger for removal of phosphate from water

  20. Theoretical investigation of the ultrafast dissociation of core-ionized water and uracil molecules immersed in liquid water

    Stia, C.R.; Fojon, O.A. [Instituto de Fisica Rosario - CONICET-Universidad Nacional de Rosario, Rosario (Argentina); Gaigeot, M.P. [Laboratoire Analyse et Modelisation pour la Biologie et l' Environnement, LAMBE, UMR-CNRS 8587, Universite d' Evry-Val-d' Essonne, 91 - Evry (France); Institut Universitaire de France, 75 - Paris (France); Vuilleumier, R. [Departement de chimie, Ecole Normale Superieure, 75 - Paris (France); Herve du Penhoat, M.A.; Politis, M.F. [Institut de Mineralogie et de Physique des Milieux Condenses, IMPMC, UMR-CNRS 7590, Universite Pierre et Marie Curie, 75 - Paris (France)

    2010-10-15

    We present a series of ab initio density functional based calculations of the fragmentation dynamics of core-ionized biomolecules. The computations are performed for pure liquid water, aqueous and isolated Uracil. Core ionization is described by replacing the 1s{sup 2} pseudopotential of one atom of the target molecule (C, N or O) with a pseudopotential for a 1s{sup 1} core-hole state. Our results predict that the dissociation of core-ionized water molecules may be reached during the lifetime of inner-shell vacancy (less than 10 fs), leading to OH bond breakage as a primary outcome. We also observe a second fragmentation channel in which total Coulomb explosion of the ionized water molecule occurs. Fragmentation pathways are found similar for pure water or when the water molecule is in the primary hydration shell of the uracil molecule. In the latter case, the proton may be transferred towards the uracil oxygen atoms. When the core hole is located on the uracil molecule, ultrafast dissociation is only observed in the aqueous environment and for nitrogen-K vacancies, resulting in proton transfers towards the hydrogen-bonded water molecule. (authors)

  1. Femtosecond spectroscopic study of the solvation of amphiphilic molecules by water

    Rezus, Y.L.A.; Bakker, H.J.

    2008-01-01

    We use polarization-resolved mid-infrared pump-probe spectroscopy to study the aqueous solvation of proline and N-methylacetamide. These molecules serve as models to study the solvation of proteins. We monitor the orientational dynamics of partly deuterated water molecules (HDO) that are present at

  2. Dynamics of water molecules in the active-site cavity of human cytochromes P450

    Rydberg, Patrik; Rod, Thomas Holm; Olsen, Lars

    2007-01-01

    We have studied the dynamics of water molecules in six crystal structures of four human cytochromes P450, 2A6, 2C8, 2C9, and 3A4, with molecular dynamics simulations. In the crystal structures, only a few water molecules are seen and the reported sizes of the active-site cavity vary a lot....... In the simulations, the cavities are completely filled with water molecules, although with approximately 20% lower density than in bulk water. The 2A6 protein differs from the other three in that it has a very small cavity with only two water molecules and no exchange with the surroundings. The other three proteins...... channels, through which there is a quite frequent exchange of water molecules (one molecule is exchanged every 30-200 ps), except in 2A6. Most of the channels are observed also in the crystal structures, but two to three channels in each protein open only during the simulations. There are no water...

  3. Structural Arrangement of Water Molecules around Highly Charged Nanoparticles: Molecular Dynamics Simulation

    Kim, Eunae; Yeom, Min Sun

    2014-01-01

    Molecular dynamics simulations were performed to understand the structural arrangement of water molecules around highly charged nanoparticles under aqueous conditions. The effect of two highly charged nanoparticles on the solvation charge asymmetry has been examined. We calculated the radial distribution functions of the components of water molecules around nanoparticles which have four charge types at two different salt concentrations. Even though the distributions of water molecules surrounding a sodium ion and a chloride ion are hardly affected by the charges of nanoparticles and the salt concentrations, those around highly charged nanoparticles are strongly influenced by the charges of nanoparticles, but hardly by the charges of nanoparticles and salt concentrations. We find that the distributions of hydrogen atoms in water molecules around one highly charged nanoparticle are dependent on the magnitude of the nanoparticle charge

  4. Quantum Electric Dipole Lattice - Water Molecules Confined to Nanocavities in Beryl

    Dressel, Martin; Zhukova, Elena S.; Thomas, Victor G.; Gorshunov, Boris P.

    2018-02-01

    Water is subject to intense investigations due to its importance in biological matter but keeps many of its secrets. Here, we unveil an even other aspect by confining H2O molecules to nanosize cages. Our THz and infrared spectra of water in the gemstone beryl evidence quantum tunneling of H2O molecules in the crystal lattice. The water molecules are spread out when confined in a nanocage. In combination with low-frequency dielectric measurements, we were also able to show that dipolar coupling among the H2O molecules leads towards a ferroelectric state at low temperatures. Upon cooling, a ferroelectric soft mode shifts through the THz range. Only quantum fluctuations prevent perfect macroscopic order to be fully achieved. Beside the significance to life science and possible application, nanoconfined water may become the prime example of a quantum electric dipolar lattice.

  5. Identification of intrinsic catalytic activity for electrochemical reduction of water molecules to generate hydrogen

    Shinagawa, Tatsuya; Takanabe, Kazuhiro

    2015-01-01

    Insufficient hydronium ion activities at near-neutral pH and under unbuffered conditions induce diffusion-limited currents for hydrogen evolution, followed by a reaction with water molecules to generate hydrogen at elevated potentials. The observed

  6. Ceramic membrane ozonator for soluble organics removal from produced water

    Siagian, U. W. R.; Dwipramana, A. S.; Perwira, S. B.; Khoiruddin; Wenten, I. G.

    2018-01-01

    In this work, the performance of ozonation for degradation of soluble organic compounds in produced water was investigated. Tubular ceramic membrane diffuser (with and without a static mixer in the lumen side) was used to facilitate contact between ozone and produced water. The ozonation was conducted at ozone flow rate of 8 L.min-1, ozone concentration of 0.4 ppm, original pH of the solution, and pressure of 1.2 bar, while the flow rates of the produced water were varied (192, 378 and 830 mL.min-1). It was found that the reduction of benzene, toluene, ethylbenzene, and xylene were 85%, 99%, 85%, and 95%, respectively. A lower liquid flow rate in a laminar state showed a better component reduction due to the longer contacting time between the liquid and the gas phase. The introduction of the static mixer in the lumen side of the membrane as a turbulence promoter provided a positive effect on the performance of the membrane diffuser. The twisted static mixer exhibited the better removal rate than the spiral static mixer.

  7. Dispersion of C(60) in natural water and removal by conventional drinking water treatment processes.

    Hyung, Hoon; Kim, Jae-Hong

    2009-05-01

    The first objective of this study is to examine the fate of C(60) under two disposal scenarios through which pristine C(60) is introduced to water containing natural organic matter (NOM). A method based on liquid-liquid extraction and HPLC to quantify nC(60) in water containing NOM was also developed. When pristine C(60) was added to water either in the form of dry C(60) or in organic solvent, it formed water stable aggregates with characteristics similar to nC(60) prepared by other methods reported in the literature. The second objective of this study is to examine the fate of the nC(60) in water treatment processes, which are the first line of defense against ingestion from potable water -- a potential route for direct human consumption. Results obtained from jar tests suggested that these colloidal aggregates of C(60) were efficiently removed by a series of alum coagulation, flocculation, sedimentation and filtration processes, while the efficiency of removal dependent on various parameters such as pH, alkalinity, NOM contents and coagulant dosage. Colloidal aggregates of functionalized C(60) could be well removed by the conventional water treatment processes but with lesser efficiency compared to those made of pristine C(60).

  8. Pollution of water sources and removal of pollutants by advanced drinking-water treatment in China.

    Wang, L; Wang, B

    2000-01-01

    The pollution of water resources and drinking water sources in China is described in this paper with basic data. About 90% of surface waters and over 60% of drinking water sources in urban areas have been polluted to different extents. The main pollutants present in drinking water sources are organic substances, ammonia nitrogen, phenols, pesticides and pathogenic micro-organisms, some of which cannot be removed effectively by the traditional water treatment processes like coagulation, sedimentation, filtration and chlorination, and the product water usually does not meet Chinese national drinking water standards, when polluted source water is treated. In some drinking-water plants in China, advanced treatment processes including activated carbon filtration and adsorption, ozonation, biological activated carbon and membrane separation have been employed for further treatment of the filtrate from a traditional treatment system producing unqualified drinking water, to make final product water meet the WHO guidelines and some developed countries' standards, as well as the Chinese national standards for drinking water. Some case studies of advanced water treatment plants are described in this paper as well.

  9. Removing NDMA (N,N-dimethylnitrosamine) from natural waters

    Mezyk, S P [California State University Long Beach, (United States); Cooper, W J [University of North Carolina at Wilmington, (United States); Bartels, D M [Argonne National Laboratory, (United States)

    2003-07-01

    Nitrosoamines are ubiquitous in water environments, and are of concern as they are potent carcinogens. In particular, N,N-dimethylnitrosamine (NDMA, (CH{sub 3}){sub 2} NNO) is volatile, and therefore has been detected around factories producing secondary amines or rocket fuel, in areas near industrial plants that use dimethylamine in organic synthesis, and even in foods and beverages that contain nitrite or which have been exposed to nitrous oxides. Various technologies have been suggested for removing trace levels of NDMA contamination from aqueous systems. However, Advanced Oxidation Technologies (AOTs), such as ozone, UV/ozone, and UV/H{sub 2}O{sub 2} , which use oxidation via the hydroxyl radical ({sup .}OH), or heterogeneous catalysis by TiO{sub 2} , sonolysis, or the electron beam process, which produce a mixture of oxidizing {sup .}OH radicals with reducing hydrated electrons (e{sup -}{sub aq} ) and hydrogen atoms ({sup .} H), may also produce unwanted stable products in the treatment. Some of these stable products, such as secondary amines, allow regeneration of NDMA to occur. To ensure that any process applied to NDMA contaminated water occurs efficiently and quantitatively a complete understanding of the chemistry involved under the conditions of use is necessary. This requires mathematical modeling of the process, which in turn needs reaction rate constants and mechanisms. In this study, absolute rate constants at room temperature for the reaction of the hydroxyl radical, hydrated electron, and hydrogen atom with NDMA in water have been determined using electron pulse radiolysis and absorption spectroscopy, (e{sup -}{sub aq} and {sup .}OH) and EPR free induction decay attenuation ({sup .}H) measurements. The specific values of (4.30{+-} 0.12) x 10 8 , (1.41 {+-} 0.02) x 10 10 , and (2.01 {+-} 0.03) x 10{sup 8} M{sup -1} s{sup -1} , respectively, demonstrate that the reductive destruction of this nitrosoamine would be the dominant removal pathway in any

  10. Removal of natural radionuclides from drinking water from private wells in Finland

    Huikuri, Pia; Salonen, Laina; Turtiainen, Tuukka

    1999-01-01

    Removal of natural radionuclides is often necessary in Finland when household water is taken from a drilled well. Removal of radionuclides by various methods from Finnish groundwaters were studied in a EU-research project, TENAWA. The results indicated that radon can be removed very efficiently (up to 99%) by applying aeration or granular activated carbon (GAC) filtration. Uranium and radium were also removed (over 94%) by using strong base anion (SBA) and strong acid cation (SAC) resins. The capability of reverse osmosis (RO) equipment to remove radionuclides was over 90% for uranium, radium and polonium. The water quality analyses indicated that water quality remained mostly good during the water treatment. (au)

  11. Efficiency of water removal from water/ethanol mixtures using supercritical carbon dioxide

    M. A. Rodrigues

    2006-06-01

    Full Text Available Techniques involving supercritical carbon dioxide have been successfully used for the formation of drug particles with controlled size distributions. However, these processes show some limitations, particularly in processing aqueous solutions. A diagram walking algorithm based on available experimental data was developed to evaluate the effect of ethanol on the efficiency of water removal processes under different process conditions. Ethanol feeding was the key parameter resulting in a tenfold increase in the efficiency of water extraction.

  12. Adsorptionof polar organic molecules at oil/water interfaces

    Aveyard, R; Chapman, J

    1975-03-15

    A study has been made of the adsorption of several esters of dicarboxylic acids at the alkane/water and the air/water interface. The adsorption of n-butanol and n-heptanol at the air/water surface also has been investigated. The surface pressure (pi) -surface area (A) isotherms are compared for the various films, and standard free energies of adsorption have been determined. Attempts have been made to fit the pi, A isotherms using surface equations of state based on the models, of both a 2-dimensional gas and a 2-dimensional solution. The solution model has proved reasonably successful for fairly dilute films at the air/water surface. At higher coverages, an equation derived by Smith for liquid expanded monolayers gives a moderately good description of films of heptanol on water. A simple application of the solution model on adsorbed monolayers at the liquid; liquid interface met with little success. However, it is found that 2-dimensional gas equations describe such systems surprisingly well for fairly low surface concentrations. (20 refs.)

  13. Roles of water molecules in bacteria and viruses

    Cox, C. S.

    1993-02-01

    In addition to water, microbes mainly comprise lipids, carbohydrates, proteins and nucleic acids. Their structure and function singularly and conjointly is affected by water activity. Desiccation leads to dramatic lipid phase changes whereas carbohydrates, proteins and nucleic acids initially suffer spontaneous, reversible low activation energy Maillard reactions forming products that more slowly re-arrange, cross-link etc. to give non-native states. While initial products spontaneously may reverse to native states by raising water activity, later products only do so through energy consumption and enzymatic activity eg. repair. Yet, native states of lipid membranes and associated enzymes are required to generate energy. Consequently, good reserves of high energy compounds (e.g. ATP) and of membrane stabilisers (e.g. trehalose) may be expected to enhance survival following drying and rehydration (e.g. anhydrobiotic organisms).

  14. Removal of glyphosate herbicide from water using biopolymer membranes.

    Carneiro, Rafael T A; Taketa, Thiago B; Gomes Neto, Reginaldo J; Oliveira, Jhones L; Campos, Estefânia V R; de Moraes, Mariana A; da Silva, Camila M G; Beppu, Marisa M; Fraceto, Leonardo F

    2015-03-15

    Enormous amounts of pesticides are manufactured and used worldwide, some of which reach soils and aquatic systems. Glyphosate is a non-selective herbicide that is effective against all types of weeds and has been used for many years. It can therefore be found as a contaminant in water, and procedures are required for its removal. This work investigates the use of biopolymeric membranes prepared with chitosan (CS), alginate (AG), and a chitosan/alginate combination (CS/AG) for the adsorption of glyphosate present in water samples. The adsorption of glyphosate by the different membranes was investigated using the pseudo-first order and pseudo-second order kinetic models, as well as the Langmuir and Freundlich isotherm models. The membranes were characterized regarding membrane solubility, swelling, mechanical, chemical and morphological properties. The results of kinetics experiments showed that adsorption equilibrium was reached within 4 h and that the CS membrane presented the best adsorption (10.88 mg of glyphosate/g of membrane), followed by the CS/AG bilayer (8.70 mg of glyphosate/g of membrane). The AG membrane did not show any adsorption capacity for this herbicide. The pseudo-second order model provided good fits to the glyphosate adsorption data on CS and CS/AG membranes, with high correlation coefficient values. Glyphosate adsorption by the membranes could be fitted by the Freundlich isotherm model. There was a high affinity between glyphosate and the CS membrane and moderate affinity in the case of the CS/AG membrane. Physico-chemical characterization of the membranes showed low values of solubility in water, indicating that the membranes are stable and not soluble in water. The SEM and AFM analysis showed evidence of the presence of glyphosate on CS membranes and on chitosan face on CS/AG membranes. The results showed that the glyphosate herbicide can be adsorbed by chitosan membranes and the proposed membrane-based methodology was successfully used to

  15. Removal of cadmium and lead from water by activated carbon

    Abdel-Shafy, H.I.; Abdel-Sabour, M.F.; El-Gamal, I.M.; Abo-El-Wafa, O.

    1989-01-01

    Adsorption of cadmium and lead from water by carbon was studied using powdered or granular carbon. The studied water artificially contaminated by cadmium and lead amounting to 1 mg/dm 3 each. Batch as well as continuous system were carried out. The batch system was used to determine the time to maintain equilibrium followed by adsorption isotherm. Results obtained by using the powered carbon were found to match with Freundlich's equation where 1/n was 2.12 and 2.096 for Cd and Pb, respectively. Corresponding constants (K) were 4.2·10 -2 and 76.0·10 -2 . The amount of powdered activated carbon required to reduce residual Cd and Pb concentration to 0.01 mg/dm 3 for each are 26.98 and 2.86 mg, respectively. Similar batch system study was carried out for the granular carbon. When granular carbon was used in a continuous system, two different contact times, namely 10 to 20 min were examined. The results obtained showed that increasing the contact time from 10 to 20 min increases the metal to carbon removal efficiency. The overall results indicated that the breakthrough point for either Cd or Pb is the reverse of their adsorption as indicated by K value. (author). 22 refs, 10 figs, 7 tabs

  16. Contamination of boreholes water by 76 pesticides molecules in the ...

    user2

    to be the cause of the degradation of the quality of sur- face and ground waters ... network and the nature of the soil generally clay lateritic with high permeability. .... 0.006 0.008 0.004 0.004 0.004 0.007 0.008 0.004 0.004 0.004 Malathion.

  17. Comparison of biological activated carbon (BAC) and membrane bioreactor (MBR) for pollutants removal in drinking water treatment.

    Tian, J Y; Chen, Z L; Liang, H; Li, X; Wang, Z Z; Li, G B

    2009-01-01

    Biological activated carbon (BAC) and membrane bioreactor (MBR) were systematically compared for the drinking water treatment from slightly polluted raw water under the same hydraulic retention time (HRT) of 0.5 h. MBR exhibited excellent turbidity removal capacity due to the separation of the membrane; while only 60% of influent turbidity was intercepted by BAC. Perfect nitrification was achieved by MBR with the 89% reduction in ammonia; by contrast, BAC only eliminated a moderate amount of influent ammonia (by 54.5%). However, BAC was able to remove more dissolved organic matter (DOM, especially for organic molecules of 3,000 approximately 500 Daltons) and corresponding disinfection by-product formation potential (DBPFP) in raw water than MBR. Unfortunately, particulate organic matter (POM) was detected in the BAC effluent. On the other hand, BAC and MBR displayed essentially the same capacity for biodegradable organic matter (BOM) removal. Fractionation of DOM showed that the removal efficiencies of hydrophobic neutrals, hydrophobic acids, weakly hydrophobic acids and hydrophilic organic matter through BAC treatment were 11.7%, 8.8%, 13.9% and 4.8% higher than that through MBR; while MBR achieved 13.8% higher hydrophobic bases removal as compared with BAC.

  18. 7 CFR 701.53 - Debris removal and water for livestock.

    2010-01-01

    ... 7 Agriculture 7 2010-01-01 2010-01-01 false Debris removal and water for livestock. 701.53 Section... RELATED PROGRAMS PREVIOUSLY ADMINISTERED UNDER THIS PART § 701.53 Debris removal and water for livestock..., and for providing water for livestock. [71 FR 30265, May 26, 2006] ...

  19. Autotrophic nitrogen removal process in a potable water treatment biofilter that simultaneously removes Mn and NH4(+)-N.

    Cai, Yan'an; Li, Dong; Liang, Yuhai; Zeng, Huiping; Zhang, Jie

    2014-11-01

    Ammonia (NH4(+)-N) removal pathways were investigated in a potable water treatment biofilter that simultaneously removes manganese (Mn) and NH4(+)-N. The results indicated a significant loss of nitrogen in the biofilter. Both the completely autotrophic nitrogen removal over nitrite (CANON) process and nitrification were more likely to contribute to NH4(+)-N removal. Moreover, the model calculation results demonstrated that the CANON process contributed significantly to the removal of NH4(+)-N. For influent NH4(+)-N levels of 1.030 and 1.749mg/L, the CANON process contribution was about 48.5% and 46.6%, respectively. The most important finding was that anaerobic ammonia oxidation (ANAMMOX) bacteria were detectable in the biofilter. It is interesting that the CANON process was effective even for such low NH4(+)-N concentrations. Copyright © 2014 Elsevier Ltd. All rights reserved.

  20. Hydroxyl and water molecule orientations in trypsin: Comparison to molecular dynamics structures

    McDowell, R.S.; Kossiakoff, A.A. [Genentech, Inc., South San Francisco, CA (United States)

    1994-12-31

    A comparison is presented of experimentally observed hydroxyl and water hydrogens in trypsin determined from neutron density maps with the results of a 140ps molecular dynamics (MD) simulation. Experimental determination of hydrogen and deuterium atom positions in molecules as large as proteins is a unique capability of neutron diffraction. The comparison addresses the degree to which a standard force-field approach can adequately describe the local electrostatic and van der Waals forces that determine the orientations of these hydrogens. Neutron densities, derived from 2.1{Angstrom} D{sub 2}O-H{sub 2}O difference Fourier maps, provide a database of 27 well-ordered hydroxyl hydrogens. Most of the simulated hydroxyl orientations are within a standard deviation of the experimentally-observed positions, including several examples in which both the simulation and the neutron density indicate that a hydroxyl group is shifted from a {open_quote}standard{close_quote} rotamer. For the most highly ordered water molecules, the hydrogen distributions calculated from the trajectory were in good agreement with neutron density; simulated water molecules that displayed multiple hydrogen bonding networks had correspondingly broadened neutron density profiles. This comparison was facilitated by development of a method to construct a pseudo 2{Angstrom} density map based on the hydrogen atom distributions from the simulation. The degree of disorder of internal water molecules is shown to result primarily from the electrostatic environment surrounding that water molecule as opposed to the cavity size available to the molecule. A method is presented for comparing the discrete observations sampled in a dynamics trajectory with the time- averaged data obtained from X-ray or neutron diffraction studies. This method is particularly useful for statically-disordered water molecules, in which the average location assigned from a trajectory may represent a site of relatively low occupancy.

  1. Modelling of decay heat removal using large water pools

    Munther, R.; Raussi, P.; Kalli, H.

    1992-01-01

    The main task for investigating of passive safety systems typical for ALWRs (Advanced Light Water Reactors) has been reviewing decay heat removal systems. The reference system for calculations has been represented in Hitachi's SBWR-concept. The calculations for energy transfer to the suppression pool were made using two different fluid mechanics codes, namely FIDAP and PHOENICS. FIDAP is based on finite element methodology and PHOENICS uses finite differences. The reason choosing these codes has been to compare their modelling and calculating abilities. The thermal stratification behaviour and the natural circulation was modelled with several turbulent flow models. Also, energy transport to the suppression pool was calculated for laminar flow conditions. These calculations required a large amount of computer resources and so the CRAY-supercomputer of the state computing centre was used. The results of the calculations indicated that the capabilities of these codes for modelling the turbulent flow regime are limited. Output from these codes should be considered carefully, and whenever possible, experimentally determined parameters should be used as input to enhance the code reliability. (orig.). (31 refs., 21 figs., 3 tabs.)

  2. ARSENIC REMOVAL FROM DRINKING WATER BY IRON REMOVAL. USEPA DEMONSTRATION PROJECT AT CLIMAX, MN. PROJECT SUMMARY

    This document is an eight page summary of the final report on arsenic demonstration project at Climax, MN (EPA/600/R-06/152). The objectives of the project are to evaluate the effectiveness of the Kinetico iron removal system in removing arsenic to meet the new arsenic maximum co...

  3. Water-mediated influence of a crowded environment on internal vibrations of a protein molecule.

    Kuffel, Anna; Zielkiewicz, Jan

    2016-02-14

    The influence of crowding on the protein inner dynamics is examined by putting a single protein molecule close to one or two neighboring protein molecules. The presence of additional molecules influences the amplitudes of protein fluctuations. Also, a weak dynamical coupling of collective velocities of surface atoms of proteins separated by a layer of water is detected. The possible mechanisms of these phenomena are described. The cross-correlation function of the collective velocities of surface atoms of two proteins was decomposed into the Fourier series. The amplitude spectrum displays a peak at low frequencies. Also, the results of principal component analysis suggest that the close presence of an additional protein molecule influences the high-amplitude, low-frequency modes in the most prominent way. This part of the spectrum covers biologically important protein motions. The neighbor-induced changes in the inner dynamics of the protein may be connected with the changes in the velocity power spectrum of interfacial water. The additional protein molecule changes the properties of solvation water and in this way it can influence the dynamics of the second protein. It is suggested that this phenomenon may be described, at first approximation, by a damped oscillator driven by an external random force. This model was successfully applied to conformationally rigid Choristoneura fumiferana antifreeze protein molecules.

  4. Rethinking Rice Preparation for Highly Efficient Removal of Inorganic Arsenic Using Percolating Cooking Water.

    Carey, Manus; Jiujin, Xiao; Gomes Farias, Júlia; Meharg, Andrew A

    2015-01-01

    A novel way of cooking rice to maximize the removal of the carcinogen inorganic arsenic (Asi) is presented here. In conventional rice cooking water and grain are in continuous contact, and it is known that the larger the water:rice cooking ratio, the more Asi removed by cooking, suggesting that the Asi in the grain is mobile in water. Experiments were designed where rice is cooked in a continual stream of percolating near boiling water, either low in Asi, or Asi free. This has the advantage of not only exposing grain to large volumes of cooking water, but also physically removes any Asi leached from the grain into the water receiving vessel. The relationship between cooking water volume and Asi removal in conventional rice cooking was demonstrated for the rice types under study. At a water-to-rice cooking ratio of 12:1, 57±5% of Asi could be removed, average of 6 wholegrain and 6 polished rice samples. Two types of percolating technology were tested, one where the cooking water was recycled through condensing boiling water steam and passing the freshly distilled hot water through the grain in a laboratory setting, and one where tap water was used to cook the rice held in an off-the-shelf coffee percolator in a domestic setting. Both approaches proved highly effective in removing Asi from the cooking rice, with up to 85% of Asi removed from individual rice types. For the recycled water experiment 59±8% and 69±10% of Asi was removed, on average, compared to uncooked rice for polished (n=27) and wholegrain (n=13) rice, respectively. For coffee percolation there was no difference between wholegrain and polished rice, and the effectiveness of Asi removal was 49±7% across 6 wholegrain and 6 polished rice samples. The manuscript explores the potential applications and further optimization of this percolating cooking water, high Asi removal, discovery.

  5. FORMATION OF ORGANIC MOLECULES AND WATER IN WARM DISK ATMOSPHERES

    Najita, Joan R. [National Optical Astronomy Observatory, 950 N. Cherry Avenue, Tucson, AZ 85719 (United States); Adamkovics, Mate; Glassgold, Alfred E. [Astronomy Department, University of California, Berkeley, CA 94720 (United States)

    2011-12-20

    Observations from Spitzer and ground-based infrared spectroscopy reveal significant diversity in the molecular emission from the inner few AU of T Tauri disks. We explore theoretically the possible origin of this diversity by expanding on our earlier thermal-chemical model of disk atmospheres. We consider how variations in grain settling, X-ray irradiation, accretion-related mechanical heating, and the oxygen-to-carbon ratio can affect the thermal and chemical properties of the atmosphere at 0.25-40 AU. We find that these model parameters can account for many properties of the detected molecular emission. The column density of the warm (200-2000 K) molecular atmosphere is sensitive to grain settling and the efficiency of accretion-related heating, which may account, at least in part, for the large range in molecular emission fluxes that have been observed. The dependence of the atmospheric properties on the model parameters may also help to explain trends that have been reported in the literature between molecular emission strength and mid-infrared color, stellar accretion rate, and disk mass. We discuss whether some of the differences between our model results and the observations (e.g., for water) indicate a role for vertical transport and freezeout in the disk midplane. We also discuss how planetesimal formation in the outer disk (beyond the snowline) may imprint a chemical signature on the inner few AU of the disk and speculate on possible observational tracers of this process.

  6. FORMATION OF ORGANIC MOLECULES AND WATER IN WARM DISK ATMOSPHERES

    Najita, Joan R.; Ádámkovics, Máté; Glassgold, Alfred E.

    2011-01-01

    Observations from Spitzer and ground-based infrared spectroscopy reveal significant diversity in the molecular emission from the inner few AU of T Tauri disks. We explore theoretically the possible origin of this diversity by expanding on our earlier thermal-chemical model of disk atmospheres. We consider how variations in grain settling, X-ray irradiation, accretion-related mechanical heating, and the oxygen-to-carbon ratio can affect the thermal and chemical properties of the atmosphere at 0.25-40 AU. We find that these model parameters can account for many properties of the detected molecular emission. The column density of the warm (200-2000 K) molecular atmosphere is sensitive to grain settling and the efficiency of accretion-related heating, which may account, at least in part, for the large range in molecular emission fluxes that have been observed. The dependence of the atmospheric properties on the model parameters may also help to explain trends that have been reported in the literature between molecular emission strength and mid-infrared color, stellar accretion rate, and disk mass. We discuss whether some of the differences between our model results and the observations (e.g., for water) indicate a role for vertical transport and freezeout in the disk midplane. We also discuss how planetesimal formation in the outer disk (beyond the snowline) may imprint a chemical signature on the inner few AU of the disk and speculate on possible observational tracers of this process.

  7. Cyclic process of simazine removal from waters by adsorption on zeolite H-Y and its regeneration by thermal treatment

    Sannino, Filomena; Ruocco, Silvia; Marocco, Antonello; Esposito, Serena; Pansini, Michele

    2012-01-01

    Highlights: ► Bringing agrochemical concentration below the law limit allowed in wastewaters. ► Regenerating the adsorbent which can be used again in the cyclic process. ► Destroying the agrochemical molecules by combustion. - Abstract: Removal of the agrochemical simazine from polluted waters through adsorption by zeolite Y in its protonic form was studied. The investigated parameters were: pH, time, initial simazine concentration and solid/liquid ratio. An iterative process of simazine removal from waters is proposed, featuring: (i) final agrochemical concentration well below 0.05 mg/dm 3 , the maximum concentration allowed by Italian laws in wastewaters; (ii) regeneration of the adsorbent by a few minutes thermal treatment in air at about 500 °C, which results in the combustion of simazine without damage of the adsorbent; (iii) destruction of the agrochemical compound by combustion.

  8. Cyclic process of simazine removal from waters by adsorption on zeolite H-Y and its regeneration by thermal treatment

    Sannino, Filomena, E-mail: fsannino@unina.it [Dipartimento di Scienze del Suolo, della Pianta, dell' Ambiente e delle Produzioni Animali, Universita di Napoli ' Federico II' , Via Universita 100, 80055 Portici (Italy); Ruocco, Silvia [Dipartimento di Scienze del Suolo, della Pianta, dell' Ambiente e delle Produzioni Animali, Universita di Napoli ' Federico II' , Via Universita 100, 80055 Portici (Italy); Marocco, Antonello; Esposito, Serena; Pansini, Michele [Laboratorio Materiali - Dipartimento di Meccanica, Strutture, Ambiente e Territorio - Universita di Cassino - Via Di Biasio 43 - 03043 Cassino (Italy)

    2012-08-30

    Highlights: Black-Right-Pointing-Pointer Bringing agrochemical concentration below the law limit allowed in wastewaters. Black-Right-Pointing-Pointer Regenerating the adsorbent which can be used again in the cyclic process. Black-Right-Pointing-Pointer Destroying the agrochemical molecules by combustion. - Abstract: Removal of the agrochemical simazine from polluted waters through adsorption by zeolite Y in its protonic form was studied. The investigated parameters were: pH, time, initial simazine concentration and solid/liquid ratio. An iterative process of simazine removal from waters is proposed, featuring: (i) final agrochemical concentration well below 0.05 mg/dm{sup 3}, the maximum concentration allowed by Italian laws in wastewaters; (ii) regeneration of the adsorbent by a few minutes thermal treatment in air at about 500 Degree-Sign C, which results in the combustion of simazine without damage of the adsorbent; (iii) destruction of the agrochemical compound by combustion.

  9. Synthesis and characterization of iron nano particles for the arsenic removal in water

    Gutierrez M, O. E.

    2011-01-01

    The synthesis of iron nanoparticles for the removal of metallic ions in polluted waters has been during the last years study topic for different world organizations. This work presents a synthesis method of conditioned coal with iron nanoparticles starting from the use of leaves of pineapple crown, with the purpose of using it in arsenic removal processes in aqueous phase. For the synthesis of this material, the leaves of the pineapple crown were used like supports structure of the iron nanoparticles. First, the pyrolysis appropriate temperature was determined. For the preparation of the support material, this had contact with a ferric nitrate and hexamine solution, because the preparation of the material and the coal synthesis were realized during the pyrolysis process, where the hexamine molecules and the ferric nitrate react, causing the reduction of the iron particles and their dispersion on the support material, obtaining as product a conditioned coal with iron nanoparticles. For the characterization of the materials were used techniques as: Scanning electron microscopy, Transmission electron microscopy, X-Rays Diffraction), X-Ray photoelectron spectroscopy and Moessbauer spectroscopy; moreover was determined the isoelectric point and the density of surface sites. The arsenic sorption capacity of the materials was evaluated by means of the methodology type lots where was determined the sorption kinetics and isotherms in terms of arsenic concentration and mass. (Author)

  10. Removal efficiency of water purifier and adsorbent for iodine, cesium, strontium, barium and zirconium in drinking water.

    Sato, Itaru; Kudo, Hiroaki; Tsuda, Shuji

    2011-01-01

    The severe incident of Fukushima Daiichi Nuclear Power Station has caused radioactive contamination of environment including drinking water. Radioactive iodine, cesium, strontium, barium and zirconium are hazardous fission products because of the high yield and/or relatively long half-life. In the present study, 4 pot-type water purifiers and several adsorbents were examined for the removal effects on these elements from drinking water. Iodide, iodate, cesium and barium were removed by all water purifiers with efficiencies about 85%, 40%, 75-90% and higher than 85%, respectively. These efficiencies lasted for 200 l, which is near the recommended limits for use of filter cartridges, without decay. Strontium was removed with initial efficiencies from 70% to 100%, but the efficiencies were slightly decreased by use. Zirconium was removed by two models, but hardly removed by the other models. Synthetic zeolite A4 efficiently removed cesium, strontium and barium, but had no effect on iodine and zirconium. Natural zeolite, mordenite, removed cesium with an efficiency as high as zeolite A4, but the removal efficiencies for strontium and barium were far less than those of zeolite A4. Activated carbon had little removal effects on these elements. In case of radioactive contamination of tap water, water purifiers may be available for convenient decontamination of drinking water in the home.

  11. Activated soil filters for removal of biocides from contaminated run-off and waste-waters

    Bester, Kai; Banzhaf, Stefan; Burkhardt, Michael

    2011-01-01

    -Octyl-isothiazolinone, Dichloro-n-octylisothiazolinone). However, this removal is a considerable improvement compared to direct discharge into surface waters or infiltration into soil without appropriate removal. In the last experiment the removal efficiencies of the different layers were studied. Though the peat layer...

  12. REMOVAL OF BERYLLIUM FROM DRINKING WATER BY CHEMICAL COAGULATION AND LIME SOFTENING

    The effectiveness of conventional drinking water treatment and lime softening was evaluated for beryllium removal from two drinking water sources. ar test studies were conducted to determine how common coagulants (aluminum sulfate and ferric chloride and lime softening performed ...

  13. Nanofiltration vs. reverse osmosis for the removal of emerging organic contaminants in water reuse

    Yangali-Quintanilla, Victor; Maeng, Sungkyu; Fujioka, Takahiro; Kennedy, Maria Dolores; Li, Zhenyu; Amya, Gary

    2011-01-01

    Reverse osmosis (RO) in existing water reuse facilities is a water industry standard. However, that approach may be questioned taking into consideration that "tight" NF can be equal or "better" than RO. NF can achieve the same removals of RO

  14. Subsurface iron and arsenic removal for drinking water treatment in Bangladesh

    Van Halem, D.

    2011-01-01

    Arsenic contamination of shallow tube well drinking water is an urgent health problem in Bangladesh. Current arsenic mitigation solutions, including (household) arsenic removal options, do not always provide a sustainable alternative for safe drinking water. A novel technology, Subsurface Arsenic

  15. Performance of water filters towards the removal of selected ...

    Organic matter removal was found to be 47%, 43%, 53%, 43.4% for bio-sand, slow sand, ceramic and membrane purifier respectively, while, fluoride removal was found to be 95.5% for bone char filter. Furthermore, filters were also assessed in terms of media availability, buying costs, operation, benefits/ effectiveness ...

  16. Influence of the effective mass of water molecule on thermal neutron scattering

    Markovic, M.

    1981-01-01

    The influence of the effective water molecule mass on the thermal neutron scattering on the nucleus of the hydrogen atom has been investigated. Besides the actual water molecule mass (M = 18) the investigations have been carried out with its two effective values (M1 = 16 and M2 = 20). The differential and total cross sections have been calculated for the incident thermal neutron energy E o = 1 eV. Investigation results show different prominence of the quantum effects and for M2 the appearance of peaks in the quasielastic scattering. (author)

  17. Sulphate Removal from Water by Carbon Residue from Biomass Gasification: Effect of Chemical Modification Methods on Sulphate Removal Efficiency

    Hanna Runtti

    2016-02-01

    Full Text Available Sulphate removal from mine water is a problem because traditional chemical precipitation does not remove all sulphates. In addition, it creates lime sediment as a secondary waste. Therefore, an inexpensive and environmental-friendly sulphate removal method is needed in addition to precipitation. In this study, carbon residues from a wood gasification process were repurposed as precursors to a suitable sorbent for SO42- ion removal. The raw material was modified using ZnCl2, BaCl2, CaCl2, FeCl3, or FeCl2. Carbon residues modified with FeCl3 were selected for further consideration because the removal efficiency toward sulphate was the highest. Batch sorption experiments were performed to evaluate the effects of the initial pH, initial SO42- ion concentration, and contact time on sulphate removal. The removal of SO42- ions using Fe-modified carbon residue was notably higher compared with unmodified carbon residue and commercially available activated carbon. The sorption data exhibited pseudo-second-order kinetics. The isotherm analysis indicated that the sorption data of Fe-modified carbon residues can be represented by the bi-Langmuir isotherm model.

  18. Removal of radionuclides from household water; Metoder foer avlaegsnande av radionuklider fraan hushaallsvatten

    Vesterbacka, P.; Turtiainen, T.; Haemaelaeinen, K.; Salonen, L.; Arvela, H.

    2007-02-15

    Research upon methods for removing radionuclides from household water was initiated in Finland in 1995. Three research projects, of which two were carried out with National Technology Agency of Finland and one with CEC, have been completed by the end of 2002. One of the main objectives of the research was to compose a guidebook for consumers and water treatment companies. Radon can be removed from household water by aeration and by activated carbon filtration. Aerators that are well designed and set up can remove over 90% of waterborne radon. The best aerators have achieved removal efficiencies that are nearly 100%. However, setting up an aeration system requires thorough planning. Also, activated carbon filtration removes radon efficiently. The removal efficiencies have been over 90%, often nearly 100%. Depending on the water quality and usage, the carbon batch inside the filter needs to be changed every 2 - 3 years. Since activated carbon filters emit gamma radiation while in use, they should not be installed inside the dwelling but in a separate building or by the well. It is recommended that uranium be removed from drinking water by anion exchange, which is the most efficient removal method for this purpose. Typically, the removal efficiencies are nearly 100%. The one exception is the so called tap filter, the removal efficiency of which depends on uranium concentration in raw water and the rate of water flow. High saline concentration in water may extricate uranium from ion exchange resin. Changes in plumbing pressure or pH-value do not have any significant influence in uranium retention. Removal efficiencies of lead and polonium vary a lot depending on the chemical form in which they occur in water. They can be reliably removed from water by reverse osmosis only. Other treatment methods, such as ion exchange and activated carbon filtration, remove lead and polonium partly. Lead and polonium are removed more efficiently when they are bound onto smaller

  19. Shear-stress-induced structural arrangement of water molecules in nanoscale Couette flow with slipping at wall boundary

    Lin, Jau-Wen

    2014-01-01

    This study investigated the structuring of water molecules in a nanoscale Couette flow with the upper plate subjected to lateral forces with various magnitudes and water slipping against a metal wall. It was found that when the upper plate is subjected to a force, the water body deforms into a parallelepiped. Water molecules in the channel are then gradually arranged into lattice positions, creating a layered structure. The structural arrangement of water molecules is caused by the water molecules accommodating themselves to the increase in energy under the application of a lateral force on the moving plate. The ordering arrangement of water molecules increases the rotational degree of freedom, allowing the molecules to increase their Coulomb potential energy through polar rotation that accounts for the energy input through the upper plate. With a force continuously applied to the upper plate, the water molecules in contact with the upper plate move forward until slip between the water and upper plate occurs. The relation between the structural arrangement of water molecules, slip at the wall, and the shear force is studied. The relation between the slip and the locking/unlocking of water molecules to metal atoms is also studied

  20. Costs of Arsenic Removal Technologies for Small Water Systems: U.S. EPA Arsenic Removal Technology Demonstration Program

    As part of the Arsenic Rule Implementation Research Program, between July 2003 and July 2011, the U.S. environmental Protection Agency (EPA) conducted 50 full-scale demonstration projects on treatment systems removing arsenic from drinking water in 26 states throughout the U.S. ...

  1. Removal of aqueous nC60 fullerene from water by low pressure membrane filtration

    Floris, R.; Nijmeijer, K.; Cornelissen, E. R.

    2016-01-01

    The potential environmental and health risks of engineered nanoparticles such as buckminsterfullerene C60 in water require their removal during the production of drinking water. We present a study focusing on (i) the removal mechanism and (ii) the elucidation of the role of the membrane pore size

  2. Removal of micropollutants from aerobically treated grey water via ozone and activated carbon

    Hernandez Leal, L.; Temmink, B.G.; Zeeman, G.; Buisman, C.J.N.

    2011-01-01

    Ozonation and adsorption onto activated carbon were tested for the removal micropollutants of personal care products from aerobically treated grey water. MilliQ water spiked with micropollutants (100–1600 µgL-1) was ozonated at a dosing rate of 1.22. In 45 min, this effectively removed (>99%):

  3. Exploratory study on prevaporation membranes for removal of water from water-crude oil emulsions

    1989-01-11

    The main objective of this study was to explore the feasibility of removing water from oil/water and water/oil emulsions by means of prevaporation. Simulated oil/water and water/oil emulsions were prepared by mixing water and kerosene of various concentrations and stabilized by adding sodium lauryl sulfate. Preliminary experiments were conducted on 12 membranes fabricated from two different materials. One membrane of each type of material was chosen for further work based on the results of preliminary tests, in which two different kinds of membranes, cellulose and polyvinylalcohol, were used. All experiments were carried out under two different down-stream pressures and various temperatures. The tests showed clearly that permeation rate increases at increasing temperatures. It was demonstrated that over 97% of water can be recovered from synthetic oil emulsions. The results also proved that both cellulose and polyvinylalcohol membranes produced permeates relatively free of oil even when the synthetic or crude oil emulsions had oil content higher than 90%. The study concluded that prevaporation was effective, but more extensive studies on various field oil emulsions with improved membrane material and systems were necessary due to the complex and site-specific characteristics of the actual field emulsions. 3 figs., 8 tabs.

  4. Micropollutant removal from black water and grey water sludge in a UASB-GAC reactor.

    Butkovskyi, A; Sevenou, L; Meulepas, R J W; Hernandez Leal, L; Zeeman, G; Rijnaarts, H H M

    2018-02-01

    The effect of granular activated carbon (GAC) addition on the removal of diclofenac, ibuprofen, metoprolol, galaxolide and triclosan in a up-flow anaerobic sludge blanket (UASB) reactor was studied. Prior to the reactor studies, batch experiments indicated that addition of activated carbon to UASB sludge can decrease micropollutant concentrations in both liquid phase and sludge. In continuous experiments, two UASB reactors were operated for 260 days at an HRT of 20 days, using a mixture of source separated black water and sludge from aerobic grey water treatment as influent. GAC (5.7 g per liter of reactor volume) was added to one of the reactors on day 138. No significant difference in COD removal and biogas production between reactors with and without GAC addition was observed. In the presence of GAC, fewer micropollutants were washed out with the effluent and a lower accumulation of micropollutants in sludge and particulate organic matter occurred, which is an advantage in micropollutant emission reduction from wastewater. However, the removal of micropollutants by adding GAC to a UASB reactor would require more activated carbon compared to effluent post-treatment. Additional research is needed to estimate the effect of bioregeneration on the lifetime of activated carbon in a UASB-GAC reactor.

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

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

    2015-01-01

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

  6. Trace Elements Removal from Waster water by Ceratophyllum ...

    Michael Horsfall

    Submerged aquatic plants can be used for the removal of Trace elements. The aim of this study was ... such as electroplating, metal finishing, textile, storage batteries, lead .... metals, Randomized Complete Block Design was used. Statistical ...

  7. Transport of water molecules through noncylindrical pores in multilayer nanoporous graphene.

    Shahbabaei, Majid; Kim, Daejoong

    2017-08-09

    In this study, molecular dynamics (MD) simulations are used to examine the water transport properties through asymmetric hourglass-shaped pores in multilayer nanoporous graphene with a constant interlayer separation of 6 Å. The properties of the tested asymmetric hourglass-shaped pores [with the models having long cone (l 1 , -P) and short cone (l 2 , +P) entrances] are compared to a symmetric pore model. The study findings indicate that the water occupancy increases across the asymmetric pore (l 1 , -P) compared to (l 2 , +P), because of the length effect. The asymmetric pore, (l 1 , -P), yields higher flux compared to (l 2 , +P) and even the symmetric model, which can be attributed to the increase in the hydrogen bonds. In addition, the single-file water molecules across the narrowest pore diameter inside the (l 2 , +P) pore exhibit higher viscosity compared to those in the (l 1 , -P) pore because of the increase in the water layering effect. Moreover, it is found that the permeability inside the multilayer hourglass-shaped pore depends on the length of the flow path of the water molecules before approaching the layer with the smallest pore diameter. The probability of dipole orientation exhibits wider distribution inside the (l 1 , -P) system compared to (l 2 , +P), implying an enhanced formation of hydrogen bonding of water molecules. This results in the fast flow of water molecules. The MD trajectory shows that the dipole orientation across the single-layer graphene has frequently flipped compared to the dipole orientation across the pores in multilayer graphene, which is maintained during the whole simulation time (although the dipole orientation has flipped for a few picoseconds at the beginning of the simulation). This can be attributed to the energy barrier induced by the individual layer. The diffusion coefficient of water molecules inside the (l 2 , +P) system increases with pressure difference, however, it decreases inside the (l 1 , -P) system because

  8. Zirconium-Based Metal–Organic Framework for Removal of Perrhenate from Water

    Banerjee, Debasis; Xu, Wenqian; Nie, Zimin; Johnson, Lewis E. V.; Coghlan, Campbell; Sushko, Maria L.; Kim, Dongsang; Schweiger, Michael J.; Kruger, Albert A.; Doonan, Christian J.; Thallapally, Praveen K.

    2016-09-06

    Efficient removal of pertechnetate (TcO4-) anions from liquid waste or melter off-gas solution for alternative treatment is one of the promising options to manage 99Tc in legacy nuclear waste. Safe immobilization of 99Tc is of major importance due to its long half-life (t1/2= 2.13 × 105 yrs) and environmental mobility. Different types of inorganic and solid state ion-exchange materials such as layered double hydroxides have been shown to absorb TcO4- anions from water. However, both high capacity and selectivity have yet to be achieved in a single material. Herein, we show that a protonated version of an ultra-stable zirconium based metal-organic framework can adsorb perrhenate (ReO4-) anions, a non-radioactive sur-rogate for TcO4-, from water even in the presence of other common anions. Synchrotron based powder X-ray diffraction and molecular simulations were used to identify the position of the adsorbed ReO4- (surrogate for TcO4-) molecule within the framework.

  9. Zirconium-Based Metal–Organic Framework for Removal of Perrhenate from Water

    Banerjee, Debasis; Xu, Wenqian; Nie, Zimin; Johnson, Lewis E. V.; Coghlan, Campbell; Sushko, Maria L.; Kim, Dongsang; Schweiger, Michael J.; Kruger, Albert A.; Doonan, Christian J.; Thallapally, Praveen K.

    2016-09-06

    Efficient removal of pertechnetate (TcO4 -) anions from liquid waste or melter off-gas solution for alternative treatment is one of the promising options to manage 99Tc in legacy nuclear waste. Safe immobilization of 99Tc is of major importance due to its long half-life (t1/2= 2.13 × 105 yrs) and environmental mobility. Different types of inorganic and solid state ion-exchange materials such as layered double hydroxides have been shown to absorb TcO4 - anions from water. However, both high capacity and selectivity have yet to be achieved in a single material. Herein, we show that a protonated version of an ultra-stable zirconium based metalorganic framework can adsorb perrhenate (ReO4 -) anions, a non-radioactive surrogate for TcO4 -, from water even in the presence of other common anions. Synchrotron based powder X-ray diffraction and molecular simulations were used to identify the position of the adsorbed ReO4 - (surrogate for TcO4 -) molecule within the framework.

  10. Removal and recovery of heavy metals of residual water industrial

    Gil P, Edison

    1999-01-01

    On the next work the state of the art about the different methods and technologies for the present removal and recovery of heavy metals for the de-contamination and control of industrial wastewater is presented. Further more, it is introduce a removal alternative for chromium (III) and chromium (V I) using a solid waste material as an adsorbent, obtaining successful results which makes this proposal circumscribe into the clean technology program and residues bag

  11. Removal of different fractions of NOM foulants during demineralized water backwashing

    Li, Sheng

    2012-09-01

    The effectiveness of demineralized water backwashing on fouling by different fractions of NOM was investigated in this study. Two types of natural surface water (Schie canal and Biesbosch reservoir) were tested to confirm the improvement of demineralized water backwashing on fouling control, and LC-OCD analysis was conducted on Schie canal water to find out which fraction of NOM was removed with those backwashes. Results derived from natural waters showed that demineralized water backwashing substantially improved UF fouling control. LC-OCD analyses showed both UF permeate and demineralized water backwashes were effective on removing part of biopolymers, but demineralized water is also effective for humic substances and a limited amount of low molecular weight substances. However, based on the LC-OCD results, even demineralized water backwashing is not effective to remove all humic substances and biopolymers rejected on the UF membranes. © 2012 Elsevier B.V. All rights reserved.

  12. Identification of intrinsic catalytic activity for electrochemical reduction of water molecules to generate hydrogen

    Shinagawa, Tatsuya

    2015-01-01

    Insufficient hydronium ion activities at near-neutral pH and under unbuffered conditions induce diffusion-limited currents for hydrogen evolution, followed by a reaction with water molecules to generate hydrogen at elevated potentials. The observed constant current behaviors at near neutral pH reflect the intrinsic electrocatalytic reactivity of the metal electrodes for water reduction. This journal is © the Owner Societies.

  13. REMOVING BIOMASS FROM WATER PONDS AND SMALL WATER RESERVOIRS BY USING NON-WOVEN FILTERS

    Jakub Nieć

    2015-10-01

    Full Text Available Small water bodies, for example garden ponds, play many functions in the environment, including biocenotic, hydrological, climatic, sozological, landfill-creative, and aesthetic. Due to their small size, these reservoirs are sensitive to external and internal factors, they are also a common natural contaminants receivers. Nonwoven filters have been investigated for several years as a useful device for treatment of domestic wastewater pre-treated in a septic tank. The aim of this study was to verify the possibility of using this type of filters for water originating from small water body purification. The effectiveness of filters were tested on the water originating from the garden pond, contained high levels of nutrients and intensive algal bloom. Research was carried out on three filters (each filter consisted of four geotextile TS 20 layers. Basic water quality indicators: total suspended solids, turbidity, COD and BOD5, temperature, pH and dissolved oxygen were measured. The research results can be considered as satisfactory in terms of mechanical treatment (removal of turbidity and total suspended solids. An important positive effect of the filters was the oxygenation of the treated water, which is especially important for fish.

  14. Effects of Water Molecule on CO Oxidation by OH: Reaction Pathways, Kinetic Barriers, and Rate Constants.

    Zhang, Linyao; Yang, Li; Zhao, Yijun; Zhang, Jiaxu; Feng, Dongdong; Sun, Shaozeng

    2017-07-06

    The water dilute oxy-fuel combustion is a clean combustion technology for near-zero emission power; and the presence of water molecule could have both kinetic and dynamic effects on combustion reactions. The reaction OH + CO → CO 2 + H, one of the most important elementary reactions, has been investigated by extensive electronic structure calculations. And the effects of a single water molecule on CO oxidation have been studied by considering the preformed OH(H 2 O) complex reacts with CO. The results show little change in the reaction pathways, but the additional water molecule actually increases the vibrationally adiabatic energy barriers (V a G ). Further thermal rate constant calculations in the temperature range of 200 to 2000 K demonstrate that the total low-pressure limit rate constant for the water assisted OH(H 2 O) + CO → CO 2 + H 2 O + H reaction is 1-2 orders lower than that of the water unassisted one, which is consistent with the change of V a G . Therefore, the hydrated radical OH(H 2 O) would actually slow down the oxidation of CO. Meanwhile, comparisons show that the M06-2X/aug-cc-pVDZ method gives a much better estimation in energy and thus is recommended to be employed for direct dynamics simulations.

  15. Integration or segregation: how do molecules behave at oil/water interfaces?

    Moore, F G; Richmond, G L

    2008-06-01

    It has been over 250 years since Benjamin Franklin, fascinated with the wave-stilling effect of oil on water, performed his famous oil-drop experiments; nevertheless, the behavior of water molecules adjacent to hydrophobic surfaces continues to fascinate today. In the 18th century, the calming of the seas seemed the most pertinent application of such knowledge; today, we understand that oil-on-water phenomena underlie a range of important chemical, physical, and biological processes, including micelle and membrane formation, protein folding, chemical separation, oil extraction, nanoparticle formation, and interfacial polymerization. Beyond classical experiments of the oil-water interface, recent interest has focused on deriving a molecular-level picture of this interface or, more generally, of water molecules positioned next to any hydrophobic surface. This Account summarizes more than a decade's work from our laboratories aimed at understanding the nature of the hydrogen bonding occurring between water and a series of organic liquids in contact. Although the common perception is that water molecules and oil molecules positioned at the interface between the immiscible liquids want nothing to do with one another, we have found that weak interactions between these hydrophilic and hydrophobic molecules lead to interesting interfacial behavior, including highly oriented water molecules and layering of the organic medium that extends several molecular layers deep into the bulk organic liquid. For some organic liquids, penetration of oriented water into the organic layer is also apparent, facilitated by molecular interactions established at the molecularly thin region of first contact between the two liquids. The studies involve a combined experimental and computational approach. The primary experimental tool that we have used is vibrational sum frequency spectroscopy (VSFS), a powerful surface-specific vibrational spectroscopic method for measuring the molecular

  16. Significantly improving trace thallium removal from surface waters during coagulation enhanced by nanosized manganese dioxide.

    Huangfu, Xiaoliu; Ma, Chengxue; Ma, Jun; He, Qiang; Yang, Chun; Jiang, Jin; Wang, Yaan; Wu, Zhengsong

    2017-02-01

    Thallium (Tl) is an element of high toxicity and significant accumulation in human body. There is an urgent need for the development of appropriate strategies for trace Tl removal in drinking water treatment plants. In this study, the efficiency and mechanism of trace Tl (0.5 μg/L) removal by conventional coagulation enhanced by nanosized manganese dioxide (nMnO 2 ) were explored in simulated water and two representative surface waters (a river water and a reservoir water obtained from Northeast China). Experimental results showed that nMnO 2 significantly improve Tl(I) removal from selected waters. The removal efficiency was dramatically higher in the simulated water, demonstrating by less than 0.1 μg/L Tl residual. The enhancement of trace Tl removal in the surface waters decreased to a certain extent. Both adjusting water pH to alkaline condition and preoxidation of Tl(I) to Tl(III) benefit trace Tl removal from surface waters. Data also indicated that competitive cation of Ca 2+ decreased the efficiency of trace Tl removal, resulting from the reduction of Tl adsorption on nMnO 2 . Humic acid could largely low Tl removal efficiency during nMnO 2 enhanced coagulation processes. Trace elemental Tl firstly adsorbed on nMnO 2 and then removed accompanying with nMnO 2 settling. The information obtained in the present study may provide a potential strategy for drinking water treatment plants threatened by trace Tl. Copyright © 2016 Elsevier Ltd. All rights reserved.

  17. Nanofiltration vs. reverse osmosis for the removal of emerging organic contaminants in water reuse

    Yangali-Quintanilla, Victor

    2011-10-01

    Reverse osmosis (RO) in existing water reuse facilities is a water industry standard. However, that approach may be questioned taking into consideration that "tight" NF can be equal or "better" than RO. NF can achieve the same removals of RO membranes when dealing with emerging organic contaminants (pharmaceuticals, pesticides, endocrine disruptors and others). Experiments using 18 emerging contaminants were performed using membranes NF200 and NF90 at bench-scale units, and for a more complete study, results of NF and RO pilot and full-scale experiments where compared to our experimental results. The removal results showed that NF can remove many emerging contaminants. The average removal by tight NF was 82% for neutral contaminants and 97% for ionic contaminants. The average removal by RO was 85% for neutral contaminants and 99% for ionic contaminants. Aquifer recharge and recovery (ARR) followed by NF can effectively remove emerging contaminants with removals over 90% when loose NF membranes are used.

  18. Study the properties of activated carbon and oxyhydroxide aluminum as sorbents for removal humic substances from natural waters

    Shiyan, L N; Machekhina, K I; Gryaznova, E N

    2016-01-01

    The present work relates to the problem of high-quality drinking water supply using processes of adsorption on activated carbon and aluminum oxyhydroxide for removal humic- type organic substances. Also the paper reports on sorbtion properties of the activeted carbon Norit SA UF and oxyhydroxide aluminum for removal humic substances. It was found out that the maximum adsorption capacity of activated carbon to organic substances is equal to 0.25 mg/mg and aluminum oxyhydroxide is equal to 0.3 mg/mg. It is shown that the maximum adsorption capacity of activated carbon Norit SA UF to iron (III) ions is equal to 0.0045 mg/mg and to silicon ions is equal to 0.024 mg/mg. Consequently, the aluminum oxyhydroxide has better adsorption characteristics in comparison with the activated carbon for removal of humic substances, iron and silicon ions. It is associated with the fact that activated carbon has a large adsorption surface, and this is due to its porous structure, but not all molecules can enter into these pores. Therefore, the fibrous structure of aluminum oxyhydroxide promotes better sorption capacity. The presented results suggest that activated carbon Norit SA UF and aluminum oxyhydroxide can be used as sorbents for removal humic substances or other organic substances from groundwater and natural waters. (paper)

  19. Water Transport and Removal in PEMFC Gas Flow Channel with Various Water Droplet Locations and Channel Surface Wettability

    Yanzhou Qin

    2018-04-01

    Full Text Available Water transport and removal in the proton exchange membrane fuel cell (PEMFC is critically important to fuel cell performance, stability, and durability. Water emerging locations on the membrane-electrode assembly (MEA surface and the channel surface wettability significantly influence the water transport and removal in PEMFC. In most simulations of water transport and removal in the PEMFC flow channel, liquid water is usually introduced at the center of the MEA surface, which is fortuitous, since water droplet can emerge randomly on the MEA surface in PEMFC. In addition, the commonly used no-slip wall boundary condition greatly confines the water sliding features on hydrophobic MEA/channel surfaces, degrading the simulation accuracy. In this study, water droplet is introduced with various locations along the channel width direction on the MEA surface, and water transport and removal is investigated numerically using an improved model incorporating the sliding flow property by using the shear wall boundary condition. It is found that the water droplet can be driven to the channel sidewall by aerodynamics when the initial water location deviates from the MEA center to a certain amount, forming the water corner flow in the flow channel. The channel surface wettability on the water transport is also studied and is shown to have a significant impact on the water corner flow in the flow channel.

  20. Use of high energy radiation in decomposition and removal of organic water pollutants

    Toelgyessy, P.

    1990-01-01

    The present review deals with the radiation chemistry of dilute aqueous solutions of organic substances emphasizing the possibility of use of high energy radiation in waste water treatment. Effects of radiation on biodegradability, toxicity to water organisms and changes in molecules of solutes showing resistance to biochemical degradation and toxicity to water organisms are discussed. (author) 31 refs

  1. Removing uranium from drinking water by metal hydroxides and anion-exchange resin

    Lee, S.Y.; Bondietti, E.A.

    1983-01-01

    Results of bench-scale testing on uranium removal from a natural water that was chosen as a good representative of uranium-bearing waters indicated that conventional coagulant and lime softening treatment removes more than 85 percent of dissolved uranium (83 μg U/L) when an optimum pH and dosage were provided. A strong base anion-exchange column is a recommended option for the treatment of private well waters containing uranium at higher than desirable levels

  2. Development of improved low-cost ceramic water filters for viral removal in the Haitian context

    Guerrero Latorre, Laura; Rusiñol Arantegui, Marta; Hundesa Gonfa, Ayalkibet; Garcia Vallès, Maite; Martínez Manent, Salvador; Joseph, Osnick; Bofill Mas, Silvia; Gironès Llop, Rosina

    2015-01-01

    Household-based water treatment (HWT) is increasingly being promoted to improve water quality and, therefore, health status in low-income countries. Ceramic water filters (CWFs) are used in many regions as sustainable HWT and have been proven to meet World Health Organization (WHO) microbiological performance targets for bacterial removal (24 log); however, the described viral removal efficiencies are insufficient to significantly reduce the associated risk of viral infection. With the object...

  3. Application of carbon nanotube technology for removal of contaminants in drinking water: A review

    Upadhyayula, Venkata K.K.; Deng, Shuguang; Mitchell, Martha C.; Smith, Geoffrey B.

    2009-01-01

    Carbon nanotube (CNT) adsorption technology has the potential to support point of use (POU) based treatment approach for removal of bacterial pathogens, natural organic matter (NOM), and cyanobacterial toxins from water systems. Unlike many microporous adsorbents, CNTs possess fibrous shape with high aspect ratio, large accessible external surface area, and well developed mesopores, all contribute to the superior removal capacities of these macromolecular biomolecules and microorganisms. This article provides a comprehensive review on application of CNTs as adsorbent media to concentrate and remove pathogens, NOM, and cyanobacterial (microcystin derivatives) toxins from water systems. The paper also surveys on consideration of CNT based adsorption filters for removal of these contaminants from cost, operational and safety standpoint. Based on the studied literature it appears that POU based CNT technology looks promising, that can possibly avoid difficulties of treating biological contaminants in conventional water treatment plants, and thereby remove the burden of maintaining the biostability of treated water in the distribution systems.

  4. Removal of arsenic from potable water by adsorptive media treatment techniques

    Yousuf, S.; Khan, S.; Aslam, M.T.; Khan, A.R.

    2012-01-01

    Summary: This study was conducted to investigate the arsenic removal efficiency of different adsorptive media from water. Different naturally occurring materials such as bauxite, plastic clay, plaster of Paris, lime, alum, and alumina etc. were used for the development of media to remove arsenic As/sup +5/ present in the artificially contaminated water. Different ratios of the selected materials were combined and ignited at 9000 C to enhance its arsenic removing efficiency. It was found that the media bauxite, plastic clay, lime (1:1:1) has a maximum removal (99%) of As +5 species from aqueous media and can be used on- site to reduce the arsenic contamination of potable water. Furthermore, the materials used in this experiment were cheaply and abundantly available within the country. The method is very simple and economically viable, for removal of arsenic from potable water. (author)

  5. Oxytetracycline removal from water by novel microbial embedding gel beads

    Wu, Nan; Pan, Peng; Zeng, Ming; Wang, Wei; Xu, Chenshan; Zhang, Zongpeng; Liu, Xinyuan; Wang, Yichao

    2018-01-01

    As a common antibiotic in aquatic environment, excessive oxytetracycline (OTC) is urgent to be removed due to its great biological toxicity. Compared with the traditional activated sludge, microbial embedding can enhance the treating efficiency. In this study, novel microbial embedding gel beads were produced with the additional agent of cyclodextrin (CD). Results show that CD could increase the mass transfer of OTC into gel beads, possibly because of its strong affinity for organic matters. In terms of OTC biodegradation, gel beads with CD were comparable to gel beads without CD, while the former’s sucrose removal efficiency was higher than the latter. The biodegradation of OTC only occurred in the presence of sucrose. The respiration test also confirmed these findings. Overall, the produced novel gel beads modified with CD could improve the removal performance of OTC.

  6. Fractionation of hydrogen and oxygen isotopes between hydrated and free water molecules in aqueous urea solution

    Kakiuchi, M.; Matsuo, S.

    1985-01-01

    Ratios of D/H and 18 O/ 16 O in the vapor phase in equilibrium with aqueous urea solution with different urea molalities were measured at 15 and 25 0 C. Under the assumption that urea solutions consist of two species, i.e., the urea-water cluster and free water, the results are interpreted to give the average hydration number, i.e., the number of water molecules per urea molecule in the urea-water cluster. Good agreement was obtained for the hydration number estimated independently from hydrogen and oxygen isotopic fractions. On the basis of hydrogen isotopic data at 25 0 C, the average hydration number of urea in the cluster is 6.3 +/- 0.8 at 2.1 m and 2.75 +/- 0.08 at saturation (20.15 m). The corresponding average hydration numbers based on oxygen isotopic data were calculated to be 6.7 +/- 2.4 at 2.1 m and 2.75 +/- 0.25 at urea saturation. HD 16 O is enriched in the urea-water cluster and H 2 18 O is enriched in free water. Isotopic partitioning between the cluster and free water is markedly different from those between hydration spheres and free water in aqueous electrolyte solutions. 29 references, 6 figures, 5 tables

  7. Structure and dynamics of water and lipid molecules in charged anionic DMPG lipid bilayer membranes

    Rønnest, A. K.; Peters, Günther H.J.; Hansen, Flemming Yssing

    2016-01-01

    Molecular dynamics simulations have been used to investigate the influence of the valency of counter-ions on the structure of freestanding bilayer membranes of the anionic 1,2-dimyristoyl-sn-glycero-3-phosphoglycerol (DMPG) lipid at 310 K and 1 atm. At this temperature, the membrane is in the fluid...... compared to experimental results and used to determine an average diffusion constant for all water molecules in the system. On extrapolating the diffusion constants inferred experimentally to a temperature of 310 K, reasonable agreement with the simulations is obtained. However, the experiments do not have...... the sensitivity to confirm the diffusion of a small component of water bound to the lipids as found in the simulations. In addition, the orientation of the dipole moment of the water molecules has been determined as a function of their depth in the membrane. Previous indirect estimates of the electrostatic...

  8. Oil and grease (O&G removal from commercial kitchen waste water using carbonised grass as a key media

    Rahmat Siti Nazahiyah

    2017-01-01

    Full Text Available Oil and grease (O&G are usually found in kitchen waste water. O&G are poorly soluble in water and can cause serious problems during the wastewater treatment. Adsorption is a fundamental process in the treatment of kitchen waste water and very economical. Activated carbon is the most effective adsorbent for this application. Therefore, the aim of the current study is to determine the potential of four materials (i.e. sand, gravel, carbonised grass (CG and clay powder as filter media for O&G removal. The CGs were originated from “Elephant Grass” and it is a fast growing plant with significant potential as carbon. The clay acts as a magnet, drawing the oil molecules out of the water and causing them to attach to the surfaces of the clay. In the current study, two filters were developed with different media materials to get the best percentage removal. Filters 1 and 2 were filled with sand, gravel and CG, and sand, gravel, CG and powder clay, respectively. Three samples were taken during peak hour between April and May 2016. The initial O&G concentration varied from 101.37 mg/l to 248.30 mg/l and the final concentration varied from none to 22.57 mg/l for both filters. The percentage removal (% of O&G were between 90.9 and 97.3 (Filter 1 and between 94.3 and 100 (Filter 2. Overall, both filters could efficiently remove O&G in the waste water and the quality of the carbonised grass proved to be as good as carbon produced from other traditional sources.

  9. Partition Coefficients of Organic Molecules in Squalane and Water/Ethanol Mixtures by Molecular Dynamics Simulations

    Lundsgaard, Rasmus; Kontogeorgis, Georgios; Economou, Ioannis G.

    2011-01-01

    coefficient can be estimated for both a small hydrophilic and a hydrophobic organic molecules between squalane (used here to mimic low density poly ethylene) and water/ethanol solutes using thermodynamic integration to calculate the free energy of solvation. Molecular dynamics simulations are performed, using...... the GROMACS software, by slowly decoupling of firstly the electrostatic and then the Lennard–Jones interactions between molecules in the simulation box. These calculations depend very much on the choice of force field. Two force fields have been tested in this work, the TraPPE-UA (united-atom) and the OPLS...

  10. Non-biological removal of organic pollutants from water

    Mersmann, A.; Kutzer, S.; Kajszika, H.; Wintrich, H.

    1995-01-01

    Contaminants present in waste water, seepage water and ground water include salts, heavy metals and organic compounds of low biodegradability. This paper considers the wide range of physico-chemical processes available for separation of such compounds from water and points out their optimal and economic range of application. Main subjects are desorption processes (air/steam stripping), adsorption processes (activated carbon, polymeric resins) and membrane separation processes. Alternative water treatment technologies (evaporation, distillation, liquid-liquid-extraction, oxidation, flocculation and precipitation) and combined processes are presented and discussed. (orig.) [de

  11. Measurements of water molecule density by tunable diode laser absorption spectroscopy in dielectric barrier discharges with gas-water interface

    Tachibana, Kunihide; Nakamura, Toshihiro; Kawasaki, Mitsuo; Morita, Tatsuo; Umekawa, Toyofumi; Kawasaki, Masahiro

    2018-01-01

    We measured water molecule (H2O) density by tunable diode-laser absorption spectroscopy (TDLAS) for applications in dielectric barrier discharges (DBDs) with a gas-water interface. First, the effects of water temperature and presence of gas flow were tested using a Petri dish filled with water and a gas injection nozzle. Second, the TDLAS system was applied to the measurements of H2O density in two types of DBDs; one was a normal (non-inverted) type with a dielectric-covered electrode above a water-filled counter electrode and the other was an inverted type with a water-suspending mesh electrode above a dielectric-covered counter electrode. The H2O density in the normal DBD was close to the density estimated from the saturated vapor pressure, whereas the density in the inverted DBD was about half of that in the former type. The difference is attributed to the upward gas flow in the latter type, that pushes the water molecules up towards the gas-water interface.

  12. Optimization of Photooxidative Removal of Phenazopyridine from Water

    Saeid, Soudabeh; Behnajady, Mohammad A.; Tolvanen, Pasi; Salmi, Tapio

    2018-05-01

    The photooxidative removal of analgesic pharmaceutical compound phenazopyridine (PhP) from aqueous solutions by UV/H2O2 system with a re-circulated photoreactor was investigated. Response surface methodology (RSM) was employed to optimize the effect of operational parameters on the photooxidative removal efficiency. The investigated variables were: the initial PhP and H2O2 concentrations, irradiation time, volume of solution and pH. The analysis of variance (ANOVA) of quadratic model demonstrated that the described model was highly significant. The predicted values of the photooxidative removal efficiency were found to be in a fair agreement with experimental values ( R 2 = 0.9832, adjusted R 2 = 0.9716). The model predicted that the optimal reaction conditions for a maximum removal of PhP (>98%) were: initial PhP concentration less than 23 mg L-1, initial concentration of H2O2 higher than 470 mg L-1, solution volume less than 500 mL, pH close to 2 and irradiation time longer than 6 min.

  13. Mo and Ni Removal from Drinking Water Using Zeolitic Tuff from Jordan

    Khalil M. Ibrahim

    2016-11-01

    Full Text Available Mo and Ni metals could be hazardous in natural waters. The initial Mo and Ni concentration in the sampled domestic drinking water of north Jordan is 550 and 110 μg/L, respectively. The efficiency of using natural faujasite–phillipsite and phillipsite–chabazite tuffs in removing Mo and Ni from contaminated drinking water was tested. Batch experiments using different weights of the adsorbent were conducted at different contact times to determine the optimum conditions. The maximal uptake capacity of Mo from drinking water was equivalent to 440–420 μg/g adsorbent. The maximum removal efficiency of Mo by faujasite–phillipsite, phillipsite–chabazite, and the modified surfactant phillipsite–chabazite tuffs were 80%, 76%, and 78%, respectively. The proportional relationship between contact time and removal efficiency of Ni from water samples was observed. The maximum removal efficiency of Ni by the zeolitic tuffs is up to 90% compared to the original groundwater sample.

  14. Local area water removal analysis of a proton exchange membrane fuel cell under gas purge conditions.

    Lee, Chi-Yuan; Lee, Yu-Ming; Lee, Shuo-Jen

    2012-01-01

    In this study, local area water content distribution under various gas purging conditions are experimentally analyzed for the first time. The local high frequency resistance (HFR) is measured using novel micro sensors. The results reveal that the liquid water removal rate in a membrane electrode assembly (MEA) is non-uniform. In the under-the-channel area, the removal of liquid water is governed by both convective and diffusive flux of the through-plane drying. Thus, almost all of the liquid water is removed within 30 s of purging with gas. However, liquid water that is stored in the under-the-rib area is not easy to remove during 1 min of gas purging. Therefore, the re-hydration of the membrane by internal diffusive flux is faster than that in the under-the-channel area. Consequently, local fuel starvation and membrane degradation can degrade the performance of a fuel cell that is started from cold.

  15. Evaluation of the Efficiency of Clay Pots in Removal of Water Impurities

    K Naddafi , AH Mahvi, S Nasseri, M Mokhtari, H Zeraati

    2005-04-01

    Full Text Available Recently, inexpensive technologies for drinking water supply in small communities are highly considered in developing countries. One of these technologies is the application of ceramic filters that are usually made of diatomaceous earth or clay soil. This research was carried out to determine the efficiency of clay pots (as a filter in removing water impurities. Pilot and the related clay parts were manufactured and its efficiency in removing TDS, hardness, NO3-, color and turbidity was measured by passing water through the clay pipes. The results showed that the clay filters had not the potential to remove hardness, EC, TDS and nitrate of water. However, they showed excellent efficiency in turbidity removal (≥ 90% and could significantly decrease the color of the water (≥ 60%.

  16. Performance of alum and assorted coagulants in turbidity removal of muddy water

    Malik, Qasim H.

    2018-03-01

    Coagulation is a primary and cost effective process in water treatment plants. Under optimum conditions, not only it effectively removes turbidity but also results in reduced sludge volume and subsequently minimizes sludge management costs. Highly turbid water from streams, canals, rivers and rain run offs was run through jar test for turbidity removal. The brown water with 250NTU turbidity when coagulated with alum and assorted coagulants proved that maximum turbidity removal was witnessed using alum dose of 0.25 g/l at ph 6 with a sedimentation time of 30 min.

  17. Experimental Investigation on the Material Removal of the Ultrasonic Vibration Assisted Abrasive Water Jet Machining Ceramics

    Tao Wang

    2017-01-01

    Full Text Available The ultrasonic vibration activated in the abrasive water jet nozzle is used to enhance the capability of the abrasive water jet machinery. The experiment devices of the ultrasonic vibration assisted abrasive water jet are established; they are composed of the ultrasonic vibration producing device, the abrasive supplying device, the abrasive water jet nozzle, the water jet intensifier pump, and so on. And the effect of process parameters such as the vibration amplitude, the system working pressure, the stand-off, and the abrasive diameter on the ceramics material removal is studied. The experimental result indicates that the depth and the volume removal are increased when the ultrasonic vibration is added on abrasive water jet. With the increase of vibration amplitude, the depth and the volume of material removal are also increased. The other parameters of the ultrasonic vibration assisted abrasive water jet also have an important role in the improvement of ceramic material erosion efficiency.

  18. EFFICIENCY OF DOMESTIC REVERSE OSMOSIS IN REMOVAL OF TRIHALOMETHANES FROM DRINKING WATER

    S. Mazloomi ، R. Nabizadeh ، S. Nasseri ، K. Naddafi ، S. Nazmara ، A. H. Mahvi

    2009-10-01

    Full Text Available The reaction of disinfectants with natural organic matters existing in water lead to the formation of Disinfection By-Products. Potentially hazardous and carcinogenic characteristics of trihalomethanes (THMs are recognized. Thus removal of THMs or its precursors are necessary for human health. The aim of this study was to study the efficiency of domestic reverse osmosis (RO in removal of trihalomethanes from drinking water. A pilot scale of RO system with Polyamide membrane as Spiral-Wound, Tape wrapping module was used. Feed solution was made by using of pure chloroform. The samples containing chloroform were analyzed using a gas chromatograph equipped with a flame ionization detector. By increasing the flow, the removal rate of chloroform decreased and with declining removal of EC, the removal of chloroform declined too. In this research, at the worst condition, the efficiency of the pilot scale reverse osmosis reached to 80 % removal of chloroform.

  19. Applicability of MIEX(®)DOC process for organics removal from NOM laden water.

    Karpinska, Anna M; Boaventura, Rui A R; Vilar, Vítor J P; Bilyk, Andrzej; Molczan, Marek

    2013-06-01

    The aim of this study was to evaluate applicability of ion exchange process for organics removal from Douro River surface water at the intake of Lever water treatment plant using magnetized ion exchange resin MIEX®. Qualitative analysis of the natural organic matter present in the surface water and prediction of its amenability to removal in conventional coagulation process were assessed. Results obtained in MIEX®DOC process kinetic batch experiments allowed determination of ion exchange efficiency in dissolved organic carbon (DOC), UV absorbing organics, and true color removal. The data were compared with the efficiencies of the conventional unit processes for organics removal at Lever WTP. MIEX®DOC process revealed to be more efficient in DOC removal than conventional treatment achieving the efficiencies in the range of 61-91 %, lowering disinfection by-products formation potential of the water. DOC removal efficiency at Lever WTP depends largely on the raw water quality and ranges from 28 % for water of moderated quality to 89 % of significantly deteriorated quality. In this work, MIEX®DOC process was also used as a reference method for the determination of contribution of anionic fraction to dissolved organic matter and selectivity of the unit processes at Lever WTP for its removal.

  20. Efficiency of lead removal from drinking water using cationic resin Purolite

    Ashour Mohammad Merganpour

    2015-01-01

    Full Text Available Background: Today, issues such as water shortage, difficulties and costs related to supplying safe water, and anomalous concentrations of heavy metals in groundwater and surface water resources, doubled the necessity of access to technical methods on removing these pollutants from water resources. Methods: In this lab study, cationic resin Purolite S-930 (with co-polymer styrene di-vinyl benzene structure was used for lead removal from drinking water containing up to 22 μg/L. Using statistical analysis and designing a full factorial experiment are the most important effective parameters on lead removal obtained through ion exchange process. Results: Analysis of response and interaction parameters of ion exchange showed that the resin column height has maximum and pH value has minimum effect on the efficiency of lead removal from aquatic environment. Trinary interaction of “effective size, flow rate, resin column high” has the most important for lead removal efficiency in this system. So the maximum efficiency was obtained at the mesh = 40, bed height =1.6 meter, and pH= 6.5. At the best operation conditions, ability to remove 95.42% of lead concentration can be achieved. Conclusion: Using the resin Purolite S-930 during 21-day service with 91.12% of mean lead removal ratio from drinking water is an economic and technical feasibility.

  1. Removal of heavy metals from water with forest based materials

    James D. McSweeny; Roger M. Rowell; George C. Chen; Thomas L. Eberhardt; Soo-Hong Min

    2006-01-01

    For 1.5 to 2.5 billion people in the world, clean water is a critical issue (Lepkowski 1999). In the U.S., it is estimated that 90% of all Americans live within 10 miles of a body of contaminated water (Hogue, 2000). The development of filters to clean our water supply is big business. It is estimated that global spending on filtration (including dust collectors, air...

  2. Oil adsorbing package, also procedure to remove oil from a water surface

    1971-05-01

    A method is given to remove oil from water to prevent water pollution. Use is made of an oil-adsorbing packet having a specific gravity which is lower than the specific gravity of water. The hull is manufactured from any material which is not a water-insoluble nonpolar material. The hull is partly permeable to water and encloses a solid oil-adsorbing compound having a large adsorbing surface. (10 claims)

  3. QSPR Study of the Retention/release Property of Odorant Molecules in Water Using Statistical Methods

    Assia Belhassan

    2017-10-01

    Full Text Available An integrated approach physicochemistry and structures property relationships has been carried out to study the odorant molecules retention/release phenomenon in the water. This study aimed to identify the molecular properties (molecular descriptors that govern this phenomenon assuming that modifying the structure leads automatically to a change in the retention/release property of odorant molecules. ACD/ChemSketch, MarvinSketch, and ChemOffice programs were used to calculate several molecular descriptors of 51 odorant molecules (15 alcohols, 11 aldehydes, 9 ketones and 16 esters. A total of 37 molecules (2/3 of the data set were placed in the training set to build the QSPR models, whereas the remaining, 14 molecules (1/3 of the data set constitute the test set. The best descriptors were selected to establish the quantitative structure property relationship (QSPR of the retention/release property of odorant molecules in water using multiple linear regression (MLR, multiple non-linear regression (MNLR and an artificial neural network (ANN methods. We propose a quantitative model according to these analyses. The models were used to predict the retention/release property of the test set compounds, and agreement between the experimental and predicted values was verified. The descriptors showed by QSPR study are used for study and designing of new compounds. The statistical results indicate that the predicted values are in good agreement with the experimental results. To validate the predictive power of the resulting models, external validation multiple correlation coefficient was calculated and has both in addition to a performant prediction power, a favorable estimation of stability. DOI: http://dx.doi.org/10.17807/orbital.v9i4.978 

  4. Calcium carbonate in the removal of iron and lead from dilute waste water

    Hautala, E; Randall, J; Goodban, A; Waiss, A Jr

    1977-01-01

    The utility of powdered CaCO/sub 3/ in the removal of lead and iron from dilute aqueous waste waters has been demonstrated and the results successfully applied to treat industrial waste water from a lead battery plant. The reclaimed water is suitable for recycling to the plant and is now being utilized with consequent economic advantages.

  5. Removal of trace organics from water by pervaporation : a technical and economic analysis

    Nijhuis, Herman Henk

    1990-01-01

    Volatile organic hydrocarbons in ground water, surface water or waste water are a continuous threat to the public health. Often traditional purification techniques cannot be applied to remove these components from aqueous solutions. In this thesis the technical and economic feasibility of

  6. ETV REPORT: REMOVAL OF CHEMICAL CONTAMINANTS IN DRINKING WATER — PALL/KINETICO PUREFECTA DRINKING WATER TREATMENT SYSTEM

    The Pall/Kinetico Purefecta™ POU drinking water treatment system was tested for removal of aldicarb, benzene, cadmium, carbofuran, cesium, chloroform, dichlorvos, dicrotophos, fenamiphos, mercury, mevinphos, oxamyl, strontium, and strychnine. The Purefecta™ employs several compon...

  7. Study of Phytoremediation Capability in Sulfate Removal from Water

    Milad Tafazoli

    2014-07-01

    Full Text Available Phytoremediation is known as a pollutants method with low cost, without operational complexity, with low energy consumption and no need for sludge disposal. In this study, hydroponic cultivation was chosen for estimation of sulfate removal as a significant sulfur compound in effluents on two fenny plants: pampas grass and bamboo.In this case, the plants were examined under two different retention times and after determining the optimum time (7 days, the main experiments were done for evaluating the plants removal efficiency and sulfate mass absorbance by plants. For better analysis, T-Test and ANOVA with significant influence (p < 0.05% were also done. Finally, the removal efficiency in pampas grass for all concentrations of 50, 200, 300, 600, 900, 1200, 1500 and 3000 mg/L were 44, 36, 34.22, 30.55, 15.93, 9.72, 7.77 and 4.44 percent, respectively, which were up to two times higher for the bamboos.

  8. The effective removal method of copper and cyanide in waste water of metal plating factories

    Jae, Won Mok; Hong, Zong Doo; Kim, Myun Sup

    1988-01-01

    To investigate the effective removal method of cooper and cyanide compounds in metal plating waste water, removal ratio of cooper and cyanide compounds in solution are measured with varying pH, concentration and contact time. As results of the present experiment, cyanide compounds in the solution are removed to 0.03mg/l or less with 5% NaOCl solution. The present result is satisfied to environmental disposal standards. The removal ratio against pH values show 99% over pH8. As results of neutral precipitation method, copper including solution are removed to 99% at pH8 in short time. The removal ratios of cyanide mixed copper solution against pH values show high efficiency(over 95%) at pH8 and 11 and removal ratios are decreased at pH10.(Author)

  9. INTERACTIVE WORKSHOP ON ARSENIC REMOVAL FROM DRINKING WATER

    In 2005, EPA's Office of Water and Office of Research and Development collaborated to present eleven arsenic training events. The workshops provided in-depth treatment technology training to help those affected; state drinking water staff, design engineers, system owners and cert...

  10. Granular activated carbon to remove agrichemicals from water

    Many growers capture and reuse irrigation water in ponds or flood irrigation tanks. Agrichemical residues can potentially build up over time and affect future crops irrigated with residue-laden water. One key chemical of concern is paclobutrazol, which is very persistent, with a half-life of around ...

  11. Molecular Dynamics Study of Water Molecules in Interlayer of 14 ^|^Aring; Tobermorite

    Yoon, Seyoon

    2013-01-01

    The molecular structure and dynamics of interlayer water of 14 Å tobermorite are investigated based on molecular dynamics (MD) simulations. Calculated structural parameters of the interlayer water configuration are in good agreement with current knowledge of the refined structure. The MD simulations provide detailed information on the position and mobility of the hydrogen and oxygen of interlayer water, as well as its self-diffusion coefficient, through the interlayer of 14 Å tobermorite. Comparison of the MD simulation results at 100 and 300 K demonstrates that water molecules in the interlayer maintain their structure but change their mobility. The dominant configuration and self-diffusion coefficient of interlayer water are obtained in this study. Copyright © 2013 Japan Concrete Institute.

  12. Removing Dissolved Silica from Waste Water with Catechol and Active Carbon

    Sasan, Koroush [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Nanoscale Sciences Dept.; Brady, Patrick [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Advanced Nuclear Energy Program; Krumhansl, James L. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Geosciences Dept.; Nenoff, Tina M. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Physical Chemical and Nano Sciences Center

    2017-01-01

    Fresh water scarcity is going to be a global great challenge in the near future because of the increasing population. Our water resources are limited and, hence, water treatment and recycling methods are the only alternatives for fresh water procurement in the upcoming decades. Water treatment and recycling methods serve to remove harmful or problematic constituents from ground, surface and waste waters prior to its consumption, industrial supply, or other uses. Scale formation in industrial and domestic installations is still an important problem during water treatment. In water treatment, silica scaling is a real and constant concern for plant operations. The focus of this study is on the viability of using a combination of catechol and active carbon to remove dissolved silica from concentrated cooling tower water (CCTW). Various analytical methods, such as ICP-MS and UV-vis, were used to understand the structure-property relationship between the material and the silica removal results. UV-Vis indicates that catechol can react with silica ions and form a silica-catecholate complex. The speciation calculation of catechol and silica shows that catechol and silica bind in the pH range of 8 – 10; there is no evidence of linkage between them in neutral and acidic pHs. The silica removal results indicate that using ~4g/L of catechol and 10g/L active carbon removes up to 50% of the dissolved silica from the CCTW.

  13. Coagulation effectiveness of graphene oxide for the removal of turbidity from raw surface water.

    Aboubaraka, Abdelmeguid E; Aboelfetoh, Eman F; Ebeid, El-Zeiny M

    2017-08-01

    This study presents the performance of graphene oxide (GO) as a coagulant in turbidity removal from naturally and artificially turbid raw surface water. GO is considered an excellent alternative to alum, the more common coagulant used in water treatment processes, to reduce the environmental release of aluminum. Effects of GO dosage, pH, and temperature on its coagulation ability were studied to determine the ideal turbidity removal conditions. The turbidity removal was ≥95% for all levels of turbid raw surface water (20, 100, and 200 NTU) at optimum conditions. The role of alkalinity in inducing turbidity removal by GO coagulation was much more pronounced upon using raw surface water samples compared with that using artificially turbid deionized water samples. Moreover, GO demonstrated high-performance removal of biological contaminants such as algae, heterotrophic bacteria, and fecal coliform bacteria by 99.0%, 98.8% and 96.0%, respectively, at a dosage of 40 mg/L. Concerning the possible environmental release of GO into the treated water following filtration process, there was no residual GO in a wide range of pH values. The outcomes of the study highlight the excellent coagulation performance of GO for the removal of turbidity and biological contaminants from raw surface water. Copyright © 2017 Elsevier Ltd. All rights reserved.

  14. Nanoparticle Zere-valent Iron Affect on As (V Removal from Drinking Water

    Hamed Koohpayehzadeh

    2012-10-01

    Full Text Available Arsenic which is present in the underground and surface water is one of the most toxic elements threating human health and animals. Arsenic has been removed in different type of ways. In this study Arsenic removal from drinking water and its decreasing rates were investigated by NZVI (nanoparticle zerovalent iron to standard limit (I.e.  0.01 mg/lit . The tests were conducted on reactor containing 100 ml water containing 1mg/L. Arsenic by virtue of Batch method. The mixture was executed in mixing was done an Oultrasnic device in order to have better mixture and complete distribution of nanoparticles in water. Then the arsenic was removed from the water by VATMAN paper of 0.45 Hm. The remained arsenic in the water was measured by ICP device. In this article the influence of the parameters including mixture time , PH ,NZVI and arcenic doses were examined . Having perfomed many tests the results showed that 1 mg arsenic can be removed 100 percent by 0.05 g NZVI in 8 min. It is possible to remove by 98 percent arsenic in 5-10 PH range. Iron nanopaticle way is an effective and rapid way to remove arsenic from water and various conditions have not considerable effect on it.

  15. Use of biochar amendments for removing bacteria from simulated tile-drainage waters

    The addition of biochar has been shown to increase bacterial removal rates by several orders of magnitude in sand-packed columns, suggesting that biochar may be a suitable amendment for use in end-of-tile filter systems to remove indicator and pathogenic microorganisms in tile-drainage waters. Addit...

  16. Centrifuge experiments for removal of aluminium turbidity from Dhruva heavy water

    Shetiya, R.S.; Unny, V.K.P.; Nayak, A.P.

    1989-01-01

    Aluminium turbidity and associated radioactivity was observed in the moderator cum coolant system of Dhruva during initial power operation. Ion exchange resin beds of the purification system were not able to remove aluminium turbidity and radioactivity of system heavy water. Centrifuge technique was used as a convenient alternative method to remove the turbidity and radioactivity. (author)

  17. Use of Bentonite in residual waters of tanneries for the removal of Cr(III)

    Echavarria Isaza, Adriana; Moreno Casaf, Monica; Ramirez Ochoa, Claudia; Tamayo Martinez, Claudia; Saldarriaga Molina, Carlos

    1998-01-01

    An efficient procedure is reported for Cr(III) removal from tannery waste waters by means of natural and chemically treated bentonites. The best result was obtained using 20 mL of effluent with 7.5 grams of Bentonite. With this quantity it was removed the total amount of chromium III present in the sample

  18. Structure and dynamics of water and lipid molecules in charged anionic DMPG lipid bilayer membranes

    Rønnest, A. K.; Peters, G. H.; Hansen, F. Y.; Taub, H.; Miskowiec, A.

    2016-01-01

    Molecular dynamics simulations have been used to investigate the influence of the valency of counter-ions on the structure of freestanding bilayer membranes of the anionic 1,2-dimyristoyl-sn-glycero-3-phosphoglycerol (DMPG) lipid at 310 K and 1 atm. At this temperature, the membrane is in the fluid phase with a monovalent counter-ion and in the gel phase with a divalent counter-ion. The diffusion constant of water as a function of its depth in the membrane has been determined from mean-square-displacement calculations. Also, calculated incoherent quasielastic neutron scattering functions have been compared to experimental results and used to determine an average diffusion constant for all water molecules in the system. On extrapolating the diffusion constants inferred experimentally to a temperature of 310 K, reasonable agreement with the simulations is obtained. However, the experiments do not have the sensitivity to confirm the diffusion of a small component of water bound to the lipids as found in the simulations. In addition, the orientation of the dipole moment of the water molecules has been determined as a function of their depth in the membrane. Previous indirect estimates of the electrostatic potential within phospholipid membranes imply an enormous electric field of 10 8 –10 9 V m −1 , which is likely to have great significance in controlling the conformation of translocating membrane proteins and in the transfer of ions and molecules across the membrane. We have calculated the membrane potential for DMPG bilayers and found ∼1 V (∼2 ⋅ 10 8 V m −1 ) when in the fluid phase with a monovalent counter-ion and ∼1.4 V (∼2.8 ⋅ 10 8 V m −1 ) when in the gel phase with a divalent counter-ion. The number of water molecules for a fully hydrated DMPG membrane has been estimated to be 9.7 molecules per lipid in the gel phase and 17.5 molecules in the fluid phase, considerably smaller than inferred experimentally for 1,2-dimyristoyl-sn-glycero-3

  19. Structure and dynamics of water and lipid molecules in charged anionic DMPG lipid bilayer membranes

    Rønnest, A. K.; Peters, G. H.; Hansen, F. Y., E-mail: flemming@kemi.dtu.dk [Department of Chemistry, Technical University of Denmark, IK 207 DTU, DK-2800 Lyngby (Denmark); Taub, H.; Miskowiec, A. [Department of Physics and Astronomy and the University of Missouri Research Reactor,University of Missouri, Columbia, Missouri 65211 (United States)

    2016-04-14

    Molecular dynamics simulations have been used to investigate the influence of the valency of counter-ions on the structure of freestanding bilayer membranes of the anionic 1,2-dimyristoyl-sn-glycero-3-phosphoglycerol (DMPG) lipid at 310 K and 1 atm. At this temperature, the membrane is in the fluid phase with a monovalent counter-ion and in the gel phase with a divalent counter-ion. The diffusion constant of water as a function of its depth in the membrane has been determined from mean-square-displacement calculations. Also, calculated incoherent quasielastic neutron scattering functions have been compared to experimental results and used to determine an average diffusion constant for all water molecules in the system. On extrapolating the diffusion constants inferred experimentally to a temperature of 310 K, reasonable agreement with the simulations is obtained. However, the experiments do not have the sensitivity to confirm the diffusion of a small component of water bound to the lipids as found in the simulations. In addition, the orientation of the dipole moment of the water molecules has been determined as a function of their depth in the membrane. Previous indirect estimates of the electrostatic potential within phospholipid membranes imply an enormous electric field of 10{sup 8}–10{sup 9} V m{sup −1}, which is likely to have great significance in controlling the conformation of translocating membrane proteins and in the transfer of ions and molecules across the membrane. We have calculated the membrane potential for DMPG bilayers and found ∼1 V (∼2 ⋅ 10{sup 8} V m{sup −1}) when in the fluid phase with a monovalent counter-ion and ∼1.4 V (∼2.8 ⋅ 10{sup 8} V m{sup −1}) when in the gel phase with a divalent counter-ion. The number of water molecules for a fully hydrated DMPG membrane has been estimated to be 9.7 molecules per lipid in the gel phase and 17.5 molecules in the fluid phase, considerably smaller than inferred experimentally for 1

  20. Water molecule-enhanced CO2 insertion in lanthanide coordination polymers

    Luo Liushan; Huang Xiaoyuan; Wang Ning; Wu Hongyan; Chen Wenbin; Feng Zihao; Zhu Huiping; Peng Xiaoling; Li Yongxian; Huang Ling; Yue Shantang; Liu Yingliang

    2009-01-01

    Two new lanthanide coordination polymers H 2 N(CH 3 ) 2 .[Eu III 2 (L 1 ) 3 (L 2 )] (1, L 1 =isophthalic acid dianion, L 2 =formic acid anion) and [La III (2,5-PDC)(L 2 )](2, 2,5-PDC=2,5-pyridinedicarboxylate dianion) were synthesized under solvothermal conditions. It is of interest that the formic ligand (L 2 ) is not contained in the stating materials, but arises from the water molecule-enhanced CO 2 insertion during the solvothermal process. Both of the two compounds exhibit complicated three dimensional sandwich-like frameworks. - Graphical abstract: Two new lanthanide coordination polymers involving water molecule-enhanced CO 2 insertion resulting in the formation of formic anion and dimethylammonium cation were synthesized under solvothermal conditions.

  1. Zeolites for nitrosamine and pharmaceutical removal from demineralised and surface water: Mechanisms and efficacy

    De Ridder, David J.; Verberk, J. Q J C; Heijman, Sebastiaan G J; Amy, Gary L.; Van Dijk, Johannis C.

    2012-01-01

    Zeolites with a high Si/Al ratio can be used as selective adsorbents in water treatment, targeting organic micropollutants which are removed poorly with activated carbon. Due to size exclusion, many Natural Organic Matter (NOM) components cannot

  2. Mercury removal from water streams through the ion exchange membrane bioreactor concept.

    Oehmen, Adrian; Vergel, Dario; Fradinho, Joana; Reis, Maria A M; Crespo, João G; Velizarov, Svetlozar

    2014-01-15

    Mercury is a highly toxic heavy metal that causes human health problems and environmental contamination. In this study, an ion exchange membrane bioreactor (IEMB) process was developed to achieve Hg(II) removal from drinking water and industrial effluents. Hg(II) transport through a cation exchange membrane was coupled with its bioreduction to Hg(0) in order to achieve Hg removal from concentrated streams, with minimal production of contaminated by-products observed. This study involves (1) membrane selection, (2) demonstration of process effectiveness for removing Hg from drinking water to below the 1ppb recommended limit, and (3) process application for treatment of concentrated water streams, where >98% of the Hg was removed, and the throughput of contaminated water was optimised through membrane pre-treatment. The IEMB process represents a novel mercury treatment technology with minimal generation of contaminated waste, thereby reducing the overall environmental impact of the process. Copyright © 2013 Elsevier B.V. All rights reserved.

  3. Naturally occurring radionuclides in drinking water before and after radon removal

    Swedjemark, G.A.; Linden, A.

    1998-06-01

    Radon removal can, with a good effect, be used to remove radon from well water. The short-lived radon progeny have been investigated in the raw and cleaned water from six private wells where radon removal based on aeration and recirculation of the water have been installed. The results from this pilot study indicate that the short-lived radon progeny in some cases follow the water to the tap for consumption to such an extent that the problem should be considered. The extent of the study is not sufficient for general conclusions. However, it is important to stress that the effective dose from the short-lived progeny is always lower than it would have been from the radon, when no radon is removed

  4. Advanced Product Water Removal and Management (APWR) Fuel Cell System, Phase I

    National Aeronautics and Space Administration — The proposed innovation is a passive, self-regulating, gravity-independent Advanced Product Water Removal and management (APWR) system for incorporation into Polymer...

  5. Advanced Product Water Removal and Management (APWR) Fuel Cell System, Phase II

    National Aeronautics and Space Administration — The proposed innovation is a passive, self-regulating, gravity-independent Advanced Product Water Removal (APWR) system for Polymer Electrolyte Membrane (PEM)...

  6. QSAR models for the removal of organic micropollutants in four different river water matrices

    Sudhakaran, Sairam; Calvin, James; Amy, Gary L.

    2012-01-01

    Ozonation is an advanced water treatment process used to remove organic micropollutants (OMPs) such as pharmaceuticals and personal care products (PPCPs). In this study, Quantitative Structure Activity Relationship (QSAR) models, for ozonation

  7. A Review of Removal of Pollutants from Water/Wastewater Using Different Types of Nanomaterials

    M. T. Amin

    2014-01-01

    Full Text Available The rapidly increasing population, depleting water resources, and climate change resulting in prolonged droughts and floods have rendered drinking water a competitive resource in many parts of the world. The development of cost-effective and stable materials and methods for providing the fresh water in adequate amounts is the need of the water industry. Traditional water/wastewater treatment technologies remain ineffective for providing adequate safe water due to increasing demand of water coupled with stringent health guidelines and emerging contaminants. Nanotechnology-based multifunctional and highly efficient processes are providing affordable solutions to water/wastewater treatments that do not rely on large infrastructures or centralized systems. The aim of the present study is to review the possible applications of the nanoparticles/fibers for the removal of pollutants from water/wastewater. The paper will briefly overview the availability and practice of different nanomaterials (particles or fibers for removal of viruses, inorganic solutes, heavy metals, metal ions, complex organic compounds, natural organic matter, nitrate, and other pollutants present in surface water, ground water, and/or industrial water. Finally, recommendations are made based on the current practices of nanotechnology applications in water industry for a stand-alone water purification unit for removing all types of contaminants from wastewater.

  8. Removing the impact of water abstractions on flow duration curves

    Masoero, Alessandro; Ganora, Daniele; Galeati, Giorgio; Laio, Francesco; Claps, Pierluigi

    2015-04-01

    Changes and interactions between human system and water cycle are getting increased attention in the scientific community. Commonly discharge data needed for water resources studies were collected close to urban or industrial settlements, thus in environments where the interest for surveying was not merely scientific, but also for socio-economical purposes. Working in non-natural environments we must take into account human impacts, like the one due to water intakes for irrigation or hydropower generation, while assessing the actual water availability and variability in a river. This can became an issue in alpine areas, where hydropower exploitation is heavy and it is common to have water abstraction before a gauge station. To have a gauge station downstream a water intake can be useful to survey the environmental flow release and to record the maximum flood values, which should not be affected by the water abstraction. Nevertheless with this configuration we are unable to define properly the water volumes available in the river, information crucial to assess low flows and investigate drought risk. This situation leads to a substantial difference between observed data (affected by the human impact) and natural data (as would have been without abstraction). A main issue is how to correct these impacts and restore the natural streamflow values. The most obvious and reliable solution would be to ask for abstraction data to water users, but these data are hard to collect. Usually they are not available, because not public or not even collected by the water exploiters. A solution could be to develop a rainfall-run-off model of the basin upstream the gauge station, but this approach needs a great number of data and parameters Working in a regional framework and not on single case studies, our goal is to provide a consistent estimate of the non-impacted statistics of the river (i.e. mean value, L-moments of variation and skewness). We proposed a parsimonious method, based

  9. Technologies for Arsenic Removal from Water: Current Status and Future Perspectives

    Nina Ricci Nicomel

    2015-12-01

    Full Text Available This review paper presents an overview of the available technologies used nowadays for the removal of arsenic species from water. Conventionally applied techniques to remove arsenic species include oxidation, coagulation-flocculation, and membrane techniques. Besides, progress has recently been made on the utility of various nanoparticles for the remediation of contaminated water. A critical analysis of the most widely investigated nanoparticles is presented and promising future research on novel porous materials, such as metal organic frameworks, is suggested.

  10. Technologies for Arsenic Removal from Water: Current Status and Future Perspectives.

    Nicomel, Nina Ricci; Leus, Karen; Folens, Karel; Van Der Voort, Pascal; Du Laing, Gijs

    2015-12-22

    This review paper presents an overview of the available technologies used nowadays for the removal of arsenic species from water. Conventionally applied techniques to remove arsenic species include oxidation, coagulation-flocculation, and membrane techniques. Besides, progress has recently been made on the utility of various nanoparticles for the remediation of contaminated water. A critical analysis of the most widely investigated nanoparticles is presented and promising future research on novel porous materials, such as metal organic frameworks, is suggested.

  11. Removal of Perfluorinated Compounds From Water using Nanoscale Zero-Valent Iron

    Arvaniti, Olga S.; Hwang, Yuhoon; Andersen, Henrik Rasmus; Nikolaos, Thomaidis S.; Athanasios, Stasinakis S.

    2014-01-01

    Perfluorinated Compounds (PFCs) are persistent micropollutants that have been detected in various environmental and biological matrices, worldwide. During the last decade, these compounds have also been detected in municipal wastewater and tap water. Due to the stability of C-F bond, the application of biological and conventional physicochemical treatment methods does not seem to remove sufficient these compounds from water and wastewater. In the current study, the removal efficiency of four ...

  12. REMOVAL OF URANIUM FROM DRINKING WATER BY CONVENTIONAL TREATMENT METHODS

    The USEPA currently does not regulate uranium in drinking water but will be revising the radionuclide regulations during 1989 and will propose a maximum contaminant level for uranium. The paper presents treatment technology information on the effectiveness of conventional method...

  13. Produced water treatment for beneficial use : emulsified oil removal

    Waisi, Basma

    2016-01-01

    The development of novel carbon material, high accessible surface area, interconnected porosity, and stable nanofiber nonwoven media for emulsified oil droplets separation from oily wastewater, in particular for oilfields produced water treatment, is discussed in this thesis. Firstly, the quantity

  14. Removal of waterborne bacteria from surface water and ...

    2013-06-24

    Jun 24, 2013 ... use of disinfectants such as chlorine and iodine), solar disin- fection and natural ... By using a list of selection and evaluation criteria, 5 household water ..... were conducted by Momba and co-authors (2010b). The authors.

  15. Removal of Animal Antibiotics for Potable Water Reclamation: A Review

    Chang, Rita

    2015-01-01

    Important classes of antibiotics that are used to treat bacterial infections in humans are also being used in food-producing animals. The overuse of antibiotics for animal food production is becoming an issue of growing concern as it promotes antibacterial resistance, compromising their efficacy and effectiveness. Low concentrations of antibiotics from feedlot runoff and wastewater discharges have been reported in surface waters and groundwaters used as drinking water sources. The presence of...

  16. Investigation of the Hydantoin Monomer and its Interaction with Water Molecules

    Gruet, Sébastien; Perez, Cristobal; Schnell, Melanie

    2017-06-01

    Hydantoin (Imidazolidine-2,4-dione, C_3H_4N_2O_2) is a five-membered heterocyclic compound of astrobiological interest. This molecule has been detected in carbonaceous chondrites [1], and its formation can rise from the presence of glycolic acid and urea, two prebiotic molecules [2]. The hydrolysis of hydantoin under acidic conditions can also produce glycine [3], an amino acid actively searched for in the interstellar medium. Spectroscopic data of hydantoin is very limited and mostly dedicated to the solid phase. The high resolution study in gas phase is restricted to the work recently published by Ozeki et al. reporting the pure rotational spectra of the ground state and two vibrational states of the molecule in the millimeter-wave region (90-370 GHz)[4]. Using chirped-pulse Fourier-transform microwave (CP-FTMW) spectroscopy, we recorded the jet-cooled rotational spectra of hydantoin with water between 2 to 8 GHz. We observed the ground state of hydantoin monomer and several water complexes with one or two water molecules. All the observed species exhibit a hyperfine structure due to the two nitrogen atoms present in the molecule, which were fully resolved and analyzed. Additional experiments with a ^{18}O enriched water sample were realized to determine the oxygen-atom positions of the water monomers. These experiments yielded accurate structural information on the preferred water binding sites. The observed complexes and the interactions that hold them together, mainly strong directional hydrogen bonds, will be presented and discussed. [1] Shimoyama, A. and Ogasawara, R., Orig. Life Evol. Biosph., 32, 165-179, 2002. DOI:10.1023/A:1016015319112. [2] Menor-Salván, C. and Marín-Yaseli, M.R., Chem. Soc. Rev., 41(16), 5404-5415, 2012. DOI:10.1039/c2cs35060b. [3] De Marcellus P., Bertrand M., Nuevo M., Westall F. and Le Sergeant d'Hendecourt L., Astrobiology. 11(9), 847-854, 2011. DOI:10.1089/ast.2011.0677. [4] Ozeki, H., Miyahara R., Ihara H., Todaka S., Kobayashi

  17. Facile synthesis of Cu(II) impregnated biochar with enhanced adsorption activity for the removal of doxycycline hydrochloride from water.

    Liu, Su; Xu, Wei-Hua; Liu, Yun-Guo; Tan, Xiao-Fei; Zeng, Guang-Ming; Li, Xin; Liang, Jie; Zhou, Zan; Yan, Zhi-Li; Cai, Xiao-Xi

    2017-08-15

    In this study, the effect factors and mechanisms of doxycycline hydrochloride (DOX) adsorption on copper nitrate modified biochar (Cu-BC) was investigated. Cu-BC absorbent was synthesized through calcination of peanut shells biomass at 450°C and then impregnation with copper nitrate. The Cu-BC has exhibited excellent sorption efficiency about 93.22% of doxycycline hydrochloride from aqueous solution, which was double higher than that of the unmodified biochar. The experimental results suggest that the adsorption efficiency of DOX on the Cu-BC is dominated by the strong complexation, electrostatic interactions between DOX molecules and the Cu-BC samples. Comprehensively considering the cost, efficiency and the application to realistic water, the Cu-BC hold the significant potential for enhancing the effectiveness to remove DOX from water. Copyright © 2017 Elsevier B.V. All rights reserved.

  18. Nuclear reactor with makeup water assist from residual heat removal system

    Corletti, M.M.; Schulz, T.L.

    1993-12-07

    A pressurized water nuclear reactor uses its residual heat removal system to make up water in the reactor coolant circuit from an in-containment refueling water supply during staged depressurization leading up to passive emergency cooling by gravity feed from the refueling water storage tank, and flooding of the containment building. When depressurization commences due to inadvertence or a manageable leak, the residual heat removal system is activated manually and prevents flooding of the containment when such action is not necessary. Operation of the passive cooling system is not impaired. A high pressure makeup water storage tank is coupled to the reactor coolant circuit, holding makeup coolant at the operational pressure of the reactor. The staged depressurization system vents the coolant circuit to the containment, thus reducing the supply of makeup coolant. The level of makeup coolant can be sensed to trigger opening of successive depressurization conduits. The residual heat removal pumps move water from the refueling water storage tank into the coolant circuit as the coolant circuit is depressurized, preventing reaching the final depressurization stage unless the makeup coolant level continues to drop. The residual heat removal system can also be coupled in a loop with the refueling water supply tank, for an auxiliary heat removal path. 2 figures.

  19. Nuclear reactor with makeup water assist from residual heat removal system

    Corletti, Michael M.; Schulz, Terry L.

    1993-01-01

    A pressurized water nuclear reactor uses its residual heat removal system to make up water in the reactor coolant circuit from an in-containment refueling water supply during staged depressurization leading up to passive emergency cooling by gravity feed from the refueling water storage tank, and flooding of the containment building. When depressurization commences due to inadvertence or a manageable leak, the residual heat removal system is activated manually and prevents flooding of the containment when such action is not necessary. Operation of the passive cooling system is not impaired. A high pressure makeup water storage tank is coupled to the reactor coolant circuit, holding makeup coolant at the operational pressure of the reactor. The staged depressurization system vents the coolant circuit to the containment, thus reducing the supply of makeup coolant. The level of makeup coolant can be sensed to trigger opening of successive depressurization conduits. The residual heat removal pumps move water from the refueling water storage tank into the coolant circuit as the coolant circuit is depressurized, preventing reaching the final depressurization stage unless the makeup coolant level continues to drop. The residual heat removal system can also be coupled in a loop with the refueling water supply tank, for an auxiliary heat removal path.

  20. Nuclear reactor with makeup water assist from residual heat removal system

    Corletti, M.M.; Schulz, T.L.

    1993-01-01

    A pressurized water nuclear reactor uses its residual heat removal system to make up water in the reactor coolant circuit from an in-containment refueling water supply during staged depressurization leading up to passive emergency cooling by gravity feed from the refueling water storage tank, and flooding of the containment building. When depressurization commences due to inadvertence or a manageable leak, the residual heat removal system is activated manually and prevents flooding of the containment when such action is not necessary. Operation of the passive cooling system is not impaired. A high pressure makeup water storage tank is coupled to the reactor coolant circuit, holding makeup coolant at the operational pressure of the reactor. The staged depressurization system vents the coolant circuit to the containment, thus reducing the supply of makeup coolant. The level of makeup coolant can be sensed to trigger opening of successive depressurization conduits. The residual heat removal pumps move water from the refueling water storage tank into the coolant circuit as the coolant circuit is depressurized, preventing reaching the final depressurization stage unless the makeup coolant level continues to drop. The residual heat removal system can also be coupled in a loop with the refueling water supply tank, for an auxiliary heat removal path. 2 figures

  1. Nitrogen and Organics Removal during Riverbank Filtration along a Reclaimed Water Restored River in Beijing, China

    Weiyan Pan

    2018-04-01

    Full Text Available Reclaimed water has been widely used to restore rivers and lakes in water scarce areas as well as in Beijing municipality, China. However, refilling the rivers with reclaimed water may result in groundwater pollution. A three-year field monitoring program was conducted to assess the effect of a riverbank filtration (RBF system on the removal of nitrogen and organics from the Qingyang River of Beijing, which is replenished with reclaimed water. Water samples from the river, sediment, and groundwater were collected for NO3-N, NH4-N, and chemical oxygen demand (COD was measured. The results indicate that about 85% of NO3-N was removed from the riverbed sediments. Approximate 92% of NH4-N was removed during the infiltration of water from river to aquifer. On average, 54% of COD was removed by RBF. The attenuation of NO3-N through RBF to the groundwater varied among seasons and was strongly related to water temperature. On the other hand, no obvious temporal variability was identified in the removal of COD. These results suggest that the RBF system is an effective barrier against NO3-N, NH4-N and COD in the Qingyang River, as well as those rivers with similar geological and climatic conditions refilled with reclaimed water.

  2. Treatment techniques for removing natural radionuclides from drinking water. Final report of the TENAWA project

    Annanmaeki, M.; Turtiainen, T.

    2000-01-01

    TENAWA project (Treatment Techniques for Removing Natural Radionuclides from Drinking Water) was carried out on a cost-shared basic with the European Commission (CEC) under the supervision of Directorate-General XII, Radiation Protection Unit. TENAWA project was started because in several European countries ground water supplies may contain high amounts of natural radionuclides. During the project both laboratory and field research was performed in order to test the applicability of different equipment and techniques for removing natural radionuclides from drinking water. The measurable objectives of the project were: to give recommendations on the most suitable methods for removing radon ( 222 Rn), uranium ( 238,234 U), radium ( 226 , 228 Ra), lead ( 210 Pb) and polonium ( 210 Po) from drinking water of different qualities (i.e. soft, hard, iron-, manganese- and humus-rich, acidic) to test commercially available equipment for its ability to remove radionuclides; to find new materials, absorbents and membranes effective in the removal of radionuclides and to issue guidelines for the treatment and disposal of radioactive wastes produced in water treatment. Radon could be removed efficiently (>95%) from domestic water supplies by both aeration and granular activated carbon (GAC) filtration. Defects in technical reliability or radon removal efficiency were observed in some aerators. The significant drawback of GAC filtration was the elevated gamma dose rates (up to 120 μSv/h) near the filter and the radioactivity of spent GAC. Aeration was found to be a suitable method for removing radon at waterworks, too. The removal efficiencies at waterworks where the aeration process was designed to remove radon or carbon dioxide were 67-99%. If the aeration process was properly designed, removal efficiencies higher than 95% could be attained. Uranium could best be removed (>95%) with strong basic anion exchange resins and radium by applying strong acidic cation exchange resins

  3. Treatment techniques for removing natural radionuclides from drinking water. Final report of the TENAWA project

    Annanmaeki, M.; Turtiainen, T. [eds.

    2000-01-01

    TENAWA project (Treatment Techniques for Removing Natural Radionuclides from Drinking Water) was carried out on a cost-shared basic with the European Commission (CEC) under the supervision of Directorate-General XII, Radiation Protection Unit. TENAWA project was started because in several European countries ground water supplies may contain high amounts of natural radionuclides. During the project both laboratory and field research was performed in order to test the applicability of different equipment and techniques for removing natural radionuclides from drinking water. The measurable objectives of the project were: to give recommendations on the most suitable methods for removing radon ({sup 222}Rn), uranium ({sup 238,234}U), radium ({sup 226}, {sup 228}Ra), lead ({sup 210}Pb) and polonium ({sup 210}Po) from drinking water of different qualities (i.e. soft, hard, iron-, manganese- and humus-rich, acidic) to test commercially available equipment for its ability to remove radionuclides; to find new materials, absorbents and membranes effective in the removal of radionuclides and to issue guidelines for the treatment and disposal of radioactive wastes produced in water treatment. Radon could be removed efficiently (>95%) from domestic water supplies by both aeration and granular activated carbon (GAC) filtration. Defects in technical reliability or radon removal efficiency were observed in some aerators. The significant drawback of GAC filtration was the elevated gamma dose rates (up to 120 {mu}Sv/h) near the filter and the radioactivity of spent GAC. Aeration was found to be a suitable method for removing radon at waterworks, too. The removal efficiencies at waterworks where the aeration process was designed to remove radon or carbon dioxide were 67-99%. If the aeration process was properly designed, removal efficiencies higher than 95% could be attained. Uranium could best be removed (>95%) with strong basic anion exchange resins and radium by applying strong

  4. Paracetamol and salicylic acid removal from contaminated water by microalgae.

    Escapa, C; Coimbra, R N; Paniagua, S; García, A I; Otero, M

    2017-12-01

    The biomass growth, pharmaceutical removal and light conversion efficiency of Chlorella sorokiniana under the presence of paracetamol (PC) and salicylic acid (SaC) were assessed and compared at two different concentrations of these pharmaceuticals (I: 25 mg l -1 , II: 250 mg l -1 ). Microalgae were resistant to these concentrations and, moreover, their growth was significantly stimulated (p ≤ 0.05) under these drugs (biomass concentration increased above 33% PCI, 35% SaCI, 13% PCII and 45% SaCII, as compared with the respective positive controls). At the steady state of the semicontinuous culture, C. sorokiniana showed removal efficiencies above 41% and 69% for PCI and PCII, respectively; and above 93% and 98% for SaCI and SaCII, respectively. Under an irradiance of 370 μE m -2  s -1 , higher quantum yields were reached by microalgae under the presence of drugs, either at dose I or II, than by the respective positive controls. These results point to C. sorokiniana as a robust strain for the bioremediation of paracetamol and salicylic acid concentrated wastewaters. Copyright © 2016 Elsevier Ltd. All rights reserved.

  5. Removal of radioactive waste waters by calcium phosphate precipitation

    Raicevic, S.; Vukovic, Z.; Mandic, M.

    1997-01-01

    The kinetics of removal of radioactive strontium by coprecipitation and sorption with amorphous calcium phosphate (ACP) which transformed into stable crystalline hydroxyapatite (HA) were investigated. The advantage of phosphate precipitation is a possibility not only for removal of radioactive strontium but also for incorporation of a strontium ion into stable structure of HA. calcium phosphate was precipitated from highly saturated solution by fast reagent mixing. Kinetic experiments were performed using strontium nitrate solution labeled with 8 5 Sr. The amount of radionuclide uptake by the solid phase was determined radiometrically at different time intervals. It was found that ACP phase firmly retains coprecipitated impurities up to 150 min, of reaction time when partial rejection of strontium into the solution occurred. In sorption experiments after prolonged time of equilibrium the firm incorporation of 8 5 Sr stable crystalline structure of HA was detected. The incorporation of 8 5 Sr into crystalline HA was analysed in detail in the paper /S. Raicevic, et. al., J. Radioanal. Nucl. Chem., Articles, Vol. 204, No 2, 1996/ (author)

  6. Simulating daily water temperatures of the Klamath River under dam removal and climate change scenarios

    Perry, Russell W.; Risley, John C.; Brewer, Scott J.; Jones, Edward C.; Rondorf, Dennis W.

    2011-01-01

    A one-dimensional daily averaged water temperature model was used to simulate Klamath River temperatures for two management alternatives under historical climate conditions and six future climate scenarios. The analysis was conducted for the Secretarial Determination on removal of four hydroelectric dams on the Klamath River. In 2012, the Secretary of the Interior will determine if dam removal and implementation of the Klamath Basin Restoration Agreement (KBRA) (Klamath Basin Restoration Agreement, 2010) will advance restoration of salmonid fisheries and is in the public interest. If the Secretary decides dam removal is appropriate, then the four dams are scheduled for removal in 2020.

  7. A Raman spectroscopy study on the effects of intermolecular hydrogen bonding on water molecules absorbed by borosilicate glass surface

    Li, Fabing; Li, Zhanlong; Wang, Ying; Wang, Shenghan; Wang, Xiaojun; Sun, Chenglin; Men, Zhiwei

    2018-05-01

    The structural forms of water/deuterated water molecules located on the surface of borosilicate capillaries have been first investigated in this study on the basis of the Raman spectral data obtained at different temperatures and under atmospheric pressure for molecules in bulk and also for molecules absorbed by borosilicate glass surface. The strongest two fundamental bands locating at 3063 cm-1 (2438 cm-1) in the recorded Raman spectra are assigned here to the Osbnd H (Osbnd D) bond stretching vibrations and they are compared with the corresponding bands observed at 3124 cm-1 (2325 cm-1) in the Raman spectrum of ice Ih. Our spectroscopic observations have indicated that the structure of water and deuterated water molecules on borosilicate surface is similar to that of ice Ih (hexagonal phase of ice). These observations have also indicated that water molecules locate on the borosilicate surface so as to construct a bilayer structure and that strong and weak intermolecular hydrogen bonds are formed between water/deuterated molecules and silanol groups on borosilicate surface. In accordance with these findings, water and deuterated water molecules at the interface of capillary have a higher melting temperature.

  8. Slurried solid media for simultaneous water purification and carbon dioxide removal from gas mixtures

    Aines, Roger D.; Bourcier, William L.; Viani, Brian

    2013-01-29

    A slurried solid media for simultaneous water purification and carbon dioxide removal from gas mixtures includes the steps of dissolving the gas mixture and carbon dioxide in water providing a gas, carbon dioxide, water mixture; adding a porous solid media to the gas, carbon dioxide, water mixture forming a slurry of gas, carbon dioxide, water, and porous solid media; heating the slurry of gas, carbon dioxide, water, and porous solid media producing steam; and cooling the steam to produce purified water and carbon dioxide.

  9. Removal of chromium (VI) from water by micro-alloyed aluminium ...

    This paper deals with Cr(VI) ion removal from water, by micro-alloyed aluminium composite (MAlC), under flow conditions. In a water environment the MAlC acts as a strong reducing agent. Dissolving it in water is accompanied by the generation of Al(III) ions and reduction of water to H2, with OH- ions. The final product is ...

  10. Removal of virus to protozoan sized particles in point-of-use ceramic water filters.

    Bielefeldt, Angela R; Kowalski, Kate; Schilling, Cherylynn; Schreier, Simon; Kohler, Amanda; Scott Summers, R

    2010-03-01

    The particle removal performance of point-of-use ceramic water filters (CWFs) was characterized in the size range of 0.02-100 microm using carboxylate-coated polystyrene fluorescent microspheres, natural particles and clay. Particles were spiked into dechlorinated tap water, and three successive water batches treated in each of six different CWFs. Particle removal generally increased with increasing size. The removal of virus-sized 0.02 and 0.1 microm spheres were highly variable between the six filters, ranging from 63 to 99.6%. For the 0.5 microm spheres removal was less variable and in the range of 95.1-99.6%, while for the 1, 2, 4.5, and 10 microm spheres removal was >99.6%. Recoating four of the CWFs with colloidal silver solution improved removal of the 0.02 microm spheres, but had no significant effects on the other particle sizes. Log removals of 1.8-3.2 were found for natural turbidity and spiked kaolin clay particles; however, particles as large as 95 microm were detected in filtered water. Copyright 2009 Elsevier Ltd. All rights reserved.

  11. Fluorescence spectroscopy as a tool for determination of organic matter removal efficiency at water treatment works

    M. Z. Bieroza

    2010-04-01

    Full Text Available Organic matter (OM in drinking water treatment is a common impediment responsible for increased coagulant and disinfectant dosages, formation of carcinogenic disinfection-by products, and microbial re-growth in distribution system. The inherent heterogeneity of OM implies the utilization of advanced analytical techniques for its characterization and assessment of removal efficiency. Here, the application of simple fluorescence excitation-emission technique to OM characterization in drinking water treatment is presented. The fluorescence data of raw and clarified water was obtained from 16 drinking water treatment works. The reduction in fulvic-like fluorescence was found to significantly correlate with OM removal measured with total organic carbon (TOC. Fluorescence properties, fulvic- and tryptophan-like regions, were found to discriminate OM fractions of different removal efficiencies. The results obtained in the study show that fluorescence spectroscopy provides a rapid and accurate characterization and quantification of OM fractions and indication of their treatability in conventional water treatment.

  12. Phytoremediation to remove nutrients and improve eutrophic stormwaters using water lettuce (Pistia stratiotes L.).

    Lu, Qin; He, Zhenli L; Graetz, Donald A; Stoffella, Peter J; Yang, Xiaoe

    2010-01-01

    Water quality impairment by nutrient enrichment from agricultural activities has been a concern worldwide. Phytoremediation technology using aquatic plants in constructed wetlands and stormwater detention ponds is increasingly applied to remediate eutrophic waters. The objectives of this study were to evaluate the effectiveness and potential of water lettuce (Pistia stratiotes L.) in removing nutrients including nitrogen (N) and phosphorus (P) from stormwater in the constructed water detention systems before it is discharged into the St. Lucie Estuary, an important surface water system in Florida, using phytoremediation technologies. In this study, water lettuce (P. stratiotes) was planted in the treatment plots of two stormwater detention ponds (East and West Ponds) in 2005-2007 and water samples from both treatment and control plots were weekly collected and analyzed for water quality properties including pH, electrical conductivity, turbidity, suspended solids, and nutrients (N and P). Optimum plant density was maintained and plant samples were collected monthly and analyzed for nutrient contents. Water quality in both ponds was improved, as evidenced by decreases in water turbidity, suspended solids, and nutrient concentrations. Water turbidity was decreased by more than 60%. Inorganic N (NH(4) (+) and NO(3) (-)) concentrations in treatment plots were more than 50% lower than those in control plots (without plant). Reductions in both PO(4) (3-) and total P were approximately 14-31%, as compared to the control plots. Water lettuce contained average N and P concentrations of 17 and 3.0 g kg(-1), respectively, and removed 190-329 kg N ha(-1) and 25-34 kg P ha(-1) annually. Many aquatic plants have been used to remove nutrients from eutrophic waters but water lettuce proved superior to most other plants in nutrient removal efficiency, owing to its rapid growth and high biomass yield potential. However, the growth and nutrient removal potential are affected by many

  13. Brazilian clay organophilization aiming its use in oil / water removal

    Mota, M.F.; Lima, W.S.; Oliveira, G.C.; Silva, M.M.; Rodrigues, M.G.F.

    2012-01-01

    Clays when subjected to modification with the addition of organic surfactant are called organoclays acquire hydrophobic character, they have an affinity for organic compounds. The organoclays can be used as adsorbents are considered promising agents in environmental control. The objective is to prepare organoclays clays from commercial use in order to remove organic contaminants. The clay used was gray, as polycationic, supplied by Süd-Chemie company and the quaternary ammonium salt was cetyltrimethylammonium bromide (Cetremide). The fresh samples and organoclay were characterized by the technique of X-ray diffraction (XRD), Cation Exchange Capacity, testing expansion and affinity with organic compounds: Swelling of Foster and adsorption capacity. The results showed appropriate conditions organophilic process. Through XRD confirmed the increase in basal spacing for the modified clay in relation to the clay in nature. (author)

  14. Dyes removal from water using low cost absorbents

    Giraldo, S.; Ramirez, A. P.; Ulloa, M.; Flórez, E.; Y Acelas, N.

    2017-12-01

    In this study, the removal capacity of low cost adsorbents during the adsorption of Methylene Blue (MB) and Congo Red (CR) at different concentrations (50 and 100mg·L-1) was evaluated. These adsorbents were produced from wood wastes (cedar and teak) by chemical activation (ZnCl2). Both studied materials, Activated Cedar (AC) and activated teak (AT) showed a good fit of their experimental data to the pseudo second order kinetic model and Langmuir isotherms. The maximum adsorption capacities for AC were 2000.0 and 444.4mg·g-1 for MB and CR, respectively, while for AT, maximum adsorption capacities of 1052.6 and 86.4mg·g-1 were found for MB and CR, respectively.

  15. Tests of some methods to remove I-131 from contaminated tap water

    Tagami, Keiko; Uchida, Shigeo

    2011-01-01

    Following the Fukushima Daiichi Nuclear Power Plant accident, iodine-131 concentrations in tap water higher than 100 Bq L"-"1 were reported by several local governments in the Kanto Plain in March 2011. To remove iodine-131 from tap water, five methods were tested in this study, that is, (1) boiling, (2) adding charcoals from oak or bamboo, (3) activated charcoals, (4) water purifiers, and (5) reverse osmosis (RO) treatments. Boiling was shown to be not effective in removing iodine-131 from tap water; indeed even higher concentrations may result from the liquid-volume reduction accompanying this process. Adding charcoals and activated charcoal treatment could not remove iodine-131, because no reduction of iodine-131 was observed in tap water samples after these treatments. Only limited effect was found with water purifiers with first several portions; no effect was expected with further water treatment. On the other hand, the RO showed high iodine-131 removal percentage of more than 95%, although the method needs about 5-10 L water to obtain 1 L of RO treated water. (author)

  16. Nutrient Removal of Grey Water from Wet Market Using Sequencing Batch Reactor

    Omar Danial; Mohd Razman Salim; Salmiati

    2016-01-01

    Fresh water scarcity has become an important issue in this world today. Water reuse is known as one of the strategies to overcome this problem. Grey water is one of the sources of reused water. Several researches were carried out on water reuse, but limited attention was focused on reusing grey water from wet market, which contains high nutrient and organic matters. This study was carried out on nutrient removal from grey water using sequencing batch reactor (SBR). The grey water sample was taken from a wet market (Pasar Peladang, Skudai). About 1L of grey water was fed into the reactor with a total volume of 4L. Anoxic-aerobic phase were divided with a ratio of 30 % - 70 % of total time respectively. Mixing was maintained at 30 rpm during the start of each cycle until settling phase to achieve uniform condition. Influent and effluent were set for 30 minutes. The SBR was operated with 3 cycles/ day, temperature 30 degree Celsius, cycle time 8 hours and hydraulic retention time (HRT) 1.2 days. Aeration at 35 L/ min was induced for ammonia conversion and assisting nitrification.. The results show that the bacteria growing in alternating anoxic/ aerobic systems could remove organic substrates and nutrient. The COD, Total Nitrogen and Total Phosphorus removal efficiencies were maximum at the levels of 94 %, 88 % and 70 % respectively. Anaerobic-Aerobic-Anoxic phase was proposed to increase the removal percentage. (author)

  17. Dry body weight: water and sodium removal targets in PD

    Krediet, Raymond T.

    2006-01-01

    BACKGROUND/AIMS: Cardiovascular mortality is high in peritoneal dialysis patients. This may be due to the presence of hypertension and fluid overload. Dietary intake of water and sodium are likely to be important, especially in anuric patients. METHODS: A review of the literature on assessment of

  18. Removal of Oil Spills from Salt Water by Magnesium, Calcium ...

    Magnesium, calcium carbonates and oxides that are widely used in cement industries were employed in studying sorption of petroleum oil spills from salt water at different condition parameters such as temperature, loading weight, degree of salinity. Treatment of magnesium, calcium carbonates and oxides by dodecyl ...

  19. Removal of ammonia from tarry water using a tubular furnace

    V.V. Grabko; V.A. Kofanova; V.M. Li; M.A. Solov' ev [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

    2009-07-15

    An ammonia-processing system without the use of live steam from OAO Alchevskkoks plant's supply network is considered. Steam obtained from the wastewater that leaves the ammonia column is used to process the excess tarry water, with the release of volatile ammonia.

  20. Removal of waterborne bacteria from surface water and ...

    In this study 5 household water-treatment devices/systems (HWTS) were constructed using inexpensive local materials (sand, gravel, zeolites and clays). They included the silver-impregnated porous pot filter (SIPP), the ceramic candle filter (CCF), the conventional biosand filter (BSF-S), a modified biosand filter with zeolites ...

  1. Turbidity and microbial load removal from river water using ...

    Several serious problems associated with the use of aluminum salts as coagulants in water and wastewater treatment, including Alzheimer's disease and related health problems have necessitated the need for alternative cost effective and more environmentally acceptable coagulants. The objective of this study, therefore, ...

  2. Kinetics of trace metal removal from tidal water by mangrove sediments under different redox conditions

    Suzuki, K.N.; Machado, E.C.; Machado, W.; Bellido, A.V.B.; Bellido, L.F.; Osso, J.A.; Lopes, R.T.

    2014-01-01

    The extent in which redox conditions can affect the removal kinetics of 58 Co and 65 Zn from tidal water by mangrove sediments was evaluated in microcosm experiments, simulating a tidal flooding period of 6 h. The average half-removal time (t 1/2 ) of 58 Co from overlaying water was slightly higher (7.3 h) under an N 2 -purged water column than under an aerated water column (5.4 h). A lower difference was found for 65 Zn (1.9 h vs. 1.5 h, respectively). Average removals of 58 Co activities from water were 54.6% (N 2 treatment) and 43.5% (aeration treatment), whereas these values were 88.0% and 92.7% for 65 Zn, respectively. Very contrasting sorption kinetics of different radiotracers occurred, while more oxidising conditions favoured only a slightly higher removal. Average 58 Co and 65 Zn inventories within sediments were 30.4% and 18.8% higher in the aeration treatment, respectively. A stronger particle-reactive behaviour was found for 65 Zn that was less redox-sensitive and more efficiently removed by sediments than 58 Co. - Highlights: ► Radiotracer experiments evidenced the role of mangrove sediments in trapping trace metals. ► Very contrasting removal kinetics from tidal water were observed for 65 Zn and 58 Co. ► Nearly 40%–50% of 58 Co activities and nearly 90% of 65 Zn activities in overlying water were removed. ► 65 Zn showed a stronger particle-reactive behaviour than observed for 58 Co. ► 58 Co was more sensitive to redox conditions in tidal water than observed for 65 Zn

  3. The effect of magnesium on partial sulphate removal from mine water as gypsum.

    Tolonen, Emma-Tuulia; Rämö, Jaakko; Lassi, Ulla

    2015-08-15

    The aim of this research was to investigate the effect of magnesium on the removal efficiency of sulphate as gypsum from mine water. The precipitation conditions were simulated with MINEQL + software and the simulation results were compared with the results from laboratory jar test experiments. Both the simulation and the laboratory results showed that magnesium in the mine water was maintaining sulphate in a soluble form as magnesium sulphate (MgSO4) at pH 9.6. Thus magnesium was preventing the removal of sulphate as gypsum (CaSO4·2H2O). However, change in the lime precipitation pH from 9.6 to 12.5 resulted in magnesium hydroxide (Mg(OH)2) precipitation and improved sulphate removal. Additionally, magnesium hydroxide could act as seed crystals for gypsum precipitation or co-precipitate sulphate further enhancing the removal of sulphate from mine water. Copyright © 2015 Elsevier Ltd. All rights reserved.

  4. Single-Molecule Imaging of DNAs with Sticky Ends at Water/Fused Silica Interface

    Isailovic, Slavica [Iowa State Univ., Ames, IA (United States)

    2005-01-01

    Total internal reflection fluorescence microscopy (TIRFM) was used to study intermolecular interactions of DNAs with unpaired (sticky) ends of different lengths at water/fused silica interface at the single-molecule level. Evanescent field residence time, linear velocity and adsorption/desorption frequency were measured in a microchannel for individual DNA molecules from T7, Lambda, and PSP3 phages at various pH values. The longest residence times and the highest adsorption/desorption frequencies at the constant flow at pH 5.5 were found for PSP3 DNA, followed by lower values for Lambda DNA, and the lowest values for T7 DNA. Since T7, Lambda, and PSP3 DNA molecules contain none, twelve and nineteen unpaired bases, respectively, it was concluded that the affinity of DNAs for the surface increases with the length of the sticky ends. This confirms that hydrophobic and hydrogen-bonding interactions between sticky ends and fused-silica surface are driving forces for DNA adsorption at the fused-silica surface. Described single-molecule methodology and results therein can be valuable for investigation of interactions in liquid chromatography, as well as for design of DNA hybridization sensors and drug delivery systems.

  5. Modeling the Release Kinetics of Poorly Water-Soluble Drug Molecules from Liposomal Nanocarriers

    Stephan Loew

    2011-01-01

    Full Text Available Liposomes are frequently used as pharmaceutical nanocarriers to deliver poorly water-soluble drugs such as temoporfin, cyclosporine A, amphotericin B, and paclitaxel to their target site. Optimal drug delivery depends on understanding the release kinetics of the drug molecules from the host liposomes during the journey to the target site and at the target site. Transfer of drugs in model systems consisting of donor liposomes and acceptor liposomes is known from experimental work to typically exhibit a first-order kinetics with a simple exponential behavior. In some cases, a fast component in the initial transfer is present, in other cases the transfer is sigmoidal. We present and analyze a theoretical model for the transfer that accounts for two physical mechanisms, collisions between liposomes and diffusion of the drug molecules through the aqueous phase. Starting with the detailed distribution of drug molecules among the individual liposomes, we specify the conditions that lead to an apparent first-order kinetic behavior. We also discuss possible implications on the transfer kinetics of (1 high drug loading of donor liposomes, (2 attractive interactions between drug molecules within the liposomes, and (3 slow transfer of drugs between the inner and outer leaflets of the liposomes.

  6. Natural organic matter removal by ion exchange at different positions in the drinking water treatment lane

    A. Grefte

    2013-01-01

    Full Text Available To guarantee a good water quality at the customers tap, natural organic matter (NOM should be (partly removed during drinking water treatment. The objective of this research was to improve the biological stability of the produced water by incorporating anion exchange (IEX for NOM removal. Different placement positions of IEX in the treatment lane (IEX positioned before coagulation, before ozonation or after slow sand filtration and two IEX configurations (MIEX® and fluidized IEX (FIX were compared on water quality as well as costs. For this purpose the pre-treatment plant at Loenderveen and production plant Weesperkarspel of Waternet were used as a case study. Both, MIEX® and FIX were able to remove NOM (mainly the HS fraction to a high extent. NOM removal can be done efficiently before ozonation and after slow sand filtration. The biological stability, in terms of assimilable organic carbon, biofilm formation rate and dissolved organic carbon, was improved by incorporating IEX for NOM removal. The operational costs were assumed to be directly dependent of the NOM removal rate and determined the difference between the IEX positions. The total costs for IEX for the three positions were approximately equal (0.0631 € m−3, however the savings on following treatment processes caused a cost reduction for the IEX positions before coagulation and before ozonation compared to IEX positioned after slow sand filtration. IEX positioned before ozonation was most cost effective and improved the biological stability of the treated water.

  7. Use of Moringa oleifera seeds for the removal of turbidity of water supply

    Gustavo Lopes Muniz

    2015-04-01

    Full Text Available Water used for human consumption may contain various impurities and solid particles in suspension that increase its turbidity level. Moringa oleifera Lam is a plant that has the potential to be used as coagulating agent in removing turbidity. The objective of this work was to evaluate the efficiency of Moringa oleifera seeds used in shells and without shells in the removal of turbidity from waters with different degrees of turbidity. Waters were used with 70, 250 and 400 initial NTU obtained synthetically. The extract of moringa seeds was prepared using unshelled and shelled seeds, seeking a simplified procedure and practice. The sedimentation times and dose of coagulant solution used were based on existing recommendations in the literature. All treatments were performed with three replicates and the averages depicted in graphs. The results showed that the use of extract of moringa seeds in shells was more efficient than with unshelled seeds in the removal of turbidity of all treatments and that the shelled seeds removed more than 99% of the initial turbidity of the water samples. Furthermore, there was a direct relationship between turbidity removal efficiency and the level of initial turbidity of the samples. The seeds were more efficient in removing turbidity of the water with a higher level of initial turbidity.

  8. The Use of Activated Alumina and Magnetic Field for the Removal Heavy Metals from Water

    Ewa Szatyłowicz

    2018-05-01

    Full Text Available The objective of this work was to verify the granular activated alumina (AA sorption properties, during the process of removing copper, lead and cadmium from water, and to monitor the impact of magnetic field (MF on the effectiveness of removing copper, lead and cadmium from water. Activated alumina adsorption is known to be an effective and inexpensive technology for the removal of selenium and arsenic from water and was suggested by EPA as a BAT for point-of-use applications. The removal of copper, lead and cadmium from water using AA and impact of magnetic field was less reported. Pilot tests showed that the use of AA sorption materials with MF impact could possibly decrease the copper, lead and cadmium content in the model water. The MF had also a positive effect on the efficiency of removal copper, lead and cadmium on AA. Increasing the efficiency of heavy metals removal in the samples had been exposed magnetic field varied from 1.9% to 8.2% compared to the control samples.

  9. Practices that Prevent the Formation of Cyanobacterial Blooms in Water Resources and remove Cyanotoxins during Physical Treatment of Drinking Water

    This book chapter presents findings of different studies on the prevention and elimination of cyanobacterial blooms in raw water resources as well as the removal of cyanotoxins during water treatment with physical processes. Initially,treatments that can be applied at the source ...

  10. Structural analysis on mutation residues and interfacial water molecules for human TIM disease understanding

    2013-01-01

    Background Human triosephosphate isomerase (HsTIM) deficiency is a genetic disease caused often by the pathogenic mutation E104D. This mutation, located at the side of an abnormally large cluster of water in the inter-subunit interface, reduces the thermostability of the enzyme. Why and how these water molecules are directly related to the excessive thermolability of the mutant have not been investigated in structural biology. Results This work compares the structure of the E104D mutant with its wild type counterparts. It is found that the water topology in the dimer interface of HsTIM is atypical, having a "wet-core-dry-rim" distribution with 16 water molecules tightly packed in a small deep region surrounded by 22 residues including GLU104. These water molecules are co-conserved with their surrounding residues in non-archaeal TIMs (dimers) but not conserved across archaeal TIMs (tetramers), indicating their importance in preserving the overall quaternary structure. As the structural permutation induced by the mutation is not significant, we hypothesize that the excessive thermolability of the E104D mutant is attributed to the easy propagation of atoms' flexibility from the surface into the core via the large cluster of water. It is indeed found that the B factor increment in the wet region is higher than other regions, and, more importantly, the B factor increment in the wet region is maintained in the deeply buried core. Molecular dynamics simulations revealed that for the mutant structure at normal temperature, a clear increase of the root-mean-square deviation is observed for the wet region contacting with the large cluster of interfacial water. Such increase is not observed for other interfacial regions or the whole protein. This clearly suggests that, in the E104D mutant, the large water cluster is responsible for the subunit interface flexibility and overall thermolability, and it ultimately leads to the deficiency of this enzyme. Conclusions Our study

  11. Removing Arsenic from Contaminated Drinking Water in Rural Bangladesh: Recent Fieldwork Results and Policy Implications

    Mathieu, Johanna L.; Gadgil, Ashok J.; Kowolik, Kristin; Addy, Susan E.A.

    2009-09-17

    ARUBA (Arsenic Removal Using Bottom Ash) has proven effective at removing high concentrations of arsenic from drinking water in Bangladesh. During fieldwork in four sub-districts of the country, ARUBA reduced arsenic levels ranging from 200 to 900 ppb to below the Bangladesh standard of 50 ppb. The technology is cost-effective because the substrate--bottom ash from coal fired power plants--is a waste material readily available in South Asia. In comparison to similar technologies, ARUBA uses less media for arsenic removal due to its high surface area to volume ratio. Hence, less waste is produced. A number of experiments were conducted in Bangladesh to determine the effectiveness of various water treatment protocols. It was found that (1) ARUBA removes more than half of the arsenic from water within five minutes of treatment, (2) ARUBA, that has settled at the bottom of a treatment vessel, continues to remove arsenic for 2-3 days, (3) ARUBA's arsenic removal efficiency can be improved through sequential partial dosing (adding a given amount of ARUBA in fractions versus all at once), and (4) allowing water to first stand for two to three days followed by treatment with ARUBA produced final arsenic levels ten times lower than treating water directly out of the well. Our findings imply a number of tradeoffs between ARUBA's effective arsenic removal capacity, treatment system costs, and waste output. These tradeoffs, some a function of arsenic-related policies in Bangladesh (e.g., waste disposal regulations), must be considered when designing an arsenic removal system. We propose that the most attractive option is to use ARUBA in communityscale water treatment centers, installed as public-private partnerships, in Bangladeshi villages.

  12. Mixing of alcohol and water molecules studied by neutron probe. Structure and dynamics

    Yoshida, Koji

    2001-01-01

    Structure of water/alcohol mixing solution was studied by three methods such as an isotope-exchanged neutron scattering method, RISM (Reference Interaction Site Model) integral equation and a neutron spin echo method. The principle of methods, experiments and results were reported. The results of experiments of water/tert-butyl alcohol (TBA) solution by the isotope-exchange neutron scattering method showed TBA molecule associated with each other through end methyl group. Especially this effect was the largest at x TBA = 0.06 and decreased with increasing the concentration of TBA. However, hydrogen bonding of TBA was very rare at x TBA = 0.06. By the partial radial distribution function obtained from RISM integral equation, it indicated that the structure of pure TBA became chain structure by hydrogen bond but changed to the structure contacted directly each hydrophobic group with increasing the concentration of water. Water/2-butoxyethanol (BE) mixing solution was measured by a neutron spin echo method. The activation energy of the diffusion coefficients obtained agreed to the energy of hydrogen bonding. The temperature response of diffusion coefficients showed the inverse of the experimental results obtained by the dynamic light scattering method. The difference between two measurement methods was different time scale and space scale. Namely, the object of the neutron scattering method is nano meter and nano second, but one of light scattering method many times over. It was proved from the above results that there was the cluster consisted of the same kind of molecule in the homogeneous two components solution, but the cluster was not stable and constantly exchanged with molecule, where the production and decay of the cluster is repeated at about nano sec. (S.Y.)

  13. Comparison of Water Turbidity Removal Efficiencies of Descurainia Sophia Seed Extract and Ferric chloride

    Mazyar Peyda

    2016-03-01

    Full Text Available Background Turbidity removal using inorganic coagulants such as iron and aluminum salts in water treatment processes causes environmental and human health concern. Historically, the use of natural coagulant to purify turbid water has been practiced for a long time. Recent research indicates that Descurainia Sophia seed can be effectively used as a natural coagulant to remove water turbidity. Method: In this work, turbidity removal efficiency of Descurainia Sophia seed extract was compared with Ferric chloride. Experiments were performed in laboratory scale. The coagulation experiments were done with kaolin as a model soil to produce turbidity in distilled water. The turbidity removal efficiency of Descurainia Sophia seed extract and Ferric chloride were conducted with jar test apparatus. In all experiments, initial turbidity was kept constant 100(NTU. Optimum combination of independent variables was used to compare two different types of coagulants. Result: The obtained results showed that Ferric chloride could remove 89.75% of the initial turbidity, while in case of Descurainia Sophia this value was 43.13%. The total organic carbon (TOC analysis of the treated water using seed extract showed an increased concentration of TOC equal to 0.99 mg/L. Conclusions: This research has shown that Descurainia Sophia seed extract has an acceptable potential in the coagulation/flocculation process to treat turbid water.

  14. Manganese removal from mine waters - investigating the occurrence and importance of manganese carbonates

    Bamforth, Selina M.; Manning, David A.C.; Singleton, Ian; Younger, Paul L.; Johnson, Karen L.

    2006-01-01

    Manganese is a common contaminant of mine water and other waste waters. Due to its high solubility over a wide pH range, it is notoriously difficult to remove from contaminated waters. Previous systems that effectively remove Mn from mine waters have involved oxidising the soluble Mn(II) species at an elevated pH using substrates such as limestone and dolomites. However it is currently unclear what effect the substrate type has upon abiotic Mn removal compared to biotic removal by in situ micro-organisms (biofilms). In order to investigate the relationship between substrate type, Mn precipitation and the biofilm community, net-alkaline Mn-contaminated mine water was treated in reactors containing one of the pure materials: dolomite, limestone, magnesite and quartzite. Mine water chemistry and Mn removal rates were monitored over a 3-month period in continuous-flow reactors. For all substrates except quartzite, Mn was removed from the mine water during this period, and Mn minerals precipitated in all cases. In addition, the plastic from which the reactor was made played a role in Mn removal. Manganese oxyhydroxides were formed in all the reactors; however, Mn carbonates (specifically kutnahorite) were only identified in the reactors containing quartzite and on the reactor plastic. Magnesium-rich calcites were identified in the dolomite and magnesite reactors, suggesting that the Mg from the substrate minerals may have inhibited Mn carbonate formation. Biofilm community development and composition on all the substrates was also monitored over the 3-month period using denaturing gradient gel electrophoresis (DGGE). The DGGE profiles in all reactors showed no change with time and no difference between substrate types, suggesting that any microbiological effects are independent of mineral substrate. The identification of Mn carbonates in these systems has important implications for the design of Mn treatment systems in that the provision of a carbonate-rich substrate

  15. Impacts of grass removal on wetting and actual water repellency in a sandy soil

    Oostindie, K.; Dekker, L.W.; Wesseling, J.G.; Geissen, V.; Ritsema, C.J.

    2016-01-01

    Soil water content and actual water repellency were assessed for soil profiles at two sites in a bare and grasscovered plot of a sand pasture, to investigate the impact of the grass removal on both properties. The soil of the plots was sampled six times in vertical transects to a depth of 33 cm

  16. URANIUM REMOVAL FROM DRINKING WATER USING A SMALL FULL-SCALE SYSTEM

    This report presents background and history of water quality, the basis for design and nine months of actual operating data for a small, full-scale strong-base ion exchange system that is used to remove uranium from a water supply serving a school in Jefferson County, CO. Informa...

  17. Removal of Uranium in Drinking Water: Brimac Environmental Services, Inc. Brimac HA 216 Adsorptive Media

    The Brimac HA 216 Adsorptive Media was tested for uranium (U) removal from a drinking water source (well water) at Grappone Toyota located in Bow, New Hampshire. The HA 216 media is a hydroxyapatite-based material. A pilot unit, consisting of a TIGG Corporation Cansorb® C-5 ste...

  18. Removal of charged micropollutants from water by ion-exchange polymers - Effects of competing electrolytes

    Bauerlein, P.S.; ter Laak, T.L.|info:eu-repo/dai/nl/304831026; Hofman-Caris, R.C.; Droge, S.T.J.|info:eu-repo/dai/nl/304834017

    2012-01-01

    A wide variety of environmental compounds of concern, e.g. pharmaceuticals or illicit drugs, are acids or bases that may predominantly be present as charged species in drinking water sources. These charged micropollutants may prove difficult to remove by currently used water treatment steps (e.g.

  19. ARSENIC REMOVAL FROM DRINKING WATER BY COAGULATION/FILTRATION AND LIME SOFTENING PLANTS

    This report documents a long term performance (one year) study of 3 water treatment plants to remove arsenic from drinking water sources. The 3 plants consisted of 2 conventional coagulation/filtration plants and 1 lime softening plant. The study involved the collecting of weekly...

  20. Fluoride Removal From Drinking Water by Electrocoagulation Using Iron and Aluminum Electrodes

    Takdastan; Emami Tabar; Neisi; Eslami

    2014-01-01

    Background Existence of fluoride in drinking water above the permissible level causes human skeletal fluorosis. Objectives Electrocoagulation by iron and aluminum electrodes was proposed for removing fluoride from drinking water. Materials and Methods Effects of different operating conditions such as treatment time, initial pH, applied voltage, type and number of electrodes, the sp...

  1. Combined ion exchange / biological denitrification for nitrate removal from ground water

    Hoek, van der J.P.

    1988-01-01

    This thesis deals with the development of a new process for nitrate removal from ground water. High nitrate concentrations in ground water are a result of fertilization in agriculture. According to a directive of the European Community the maximum admissible concentration of nitrate in

  2. Stover removal effects on seasonal soil water availability under full and deficit irrigation

    Removing corn (Zea mays L.) stover for livestock feed or bioenergy feedstock may impact water availability in the soil profile to support crop growth. The role of stover in affecting soil profile water availability will depend on annual rainfall inputs as well as irrigation level. To assess how res...

  3. Experimental Application of an Advanced Separation Process for NOM Removal from Surface Drinking Water Supply

    Arianna Callegari

    2017-10-01

    Full Text Available Natural organic matter (NOM in drinking water supplies significantly impacts on water supply quality and treatment, due to observed reactivity with many dissolved and particulate species. Several technologies are used nowadays to remove NOM from the water supply. The evolution of water-related directives, and progressively more restrictive standards for drinking water, however, call for the investigation of advanced, more efficient, and cost-effective water treatment processes. This paper contains a brief overview on the state-of-the-art methods for NOM removal from supply waters, and describes the experimental application of an advanced technology, tested and validated at the pilot scale on the water supply source of a town in Poland. The process allowed significant removal of natural organic matter (about 50% as Dissolved Organic Carbon and turbidity (from 50% to 90%, however, these results requested significant additions of powdered activated carbon. The key to success of this type of process is a correct setup with the identification of optimal types and dosages of reagents. Based on the results of the tests conducted it is foreseeable that this technology could be used onsite, not only for removal of NOM, but also of other hard-to-tackle pollutants potentially contained in the freshwater supply and not presently considered.

  4. Microbial Community Profile of a Lead Service Line Removed from a Drinking Water Distribution System▿

    White, Colin; Tancos, Matthew; Lytle, Darren A.

    2011-01-01

    A corroded lead service line was removed from a drinking water distribution system, and the microbial community was profiled using 16S rRNA gene techniques. This is the first report of the characterization of a biofilm on the surface of a corroded lead drinking water service line. The majority of phylotypes have been linked to heavy-metal-contaminated environments. PMID:21652741

  5. Autotrophic nitrogen removal from low strength waste water at low temperature

    Hendrickx, T.L.G.; Wang, Y.; Kampman, C.; Zeeman, G.; Temmink, B.G.; Buisman, C.J.N.

    2012-01-01

    Direct anaerobic treatment of municipal waste waters allows for energy recovery in the form of biogas. A further decrease in the energy requirement for waste water treatment can be achieved by removing the ammonium in the anaerobic effluent with an autotrophic process, such as anammox. Until now,

  6. Nitrogen Removal from Digested Black Water by One-stage Partial Nitritation and Anammox

    Vlaeminck, S.E.; Terada, Akihiko; Smets, Barth F.

    2009-01-01

    This study assessed the technical feasibility to treat digested black water from vacuum toilets (> 1000 mg NH4+-N L-1) in a lab-scale oxygen-limited autotrophic nitrification/denitrification (OLAND) rotating biological contactor. After an adaptation period of 2.5 months, a stable. nitrogen removal...... conversion was very low, in contrast to the high specific AnAOB activity. DGGE analysis showed that the dominant AerAOB and AnAOB species were resistant to the transition from synthetic medium to digested black water. This study demonstrates high-rate nitrogen removal from digested black water by one...

  7. Overview of technologies for removal of methyl tert-butyl ether (MTBE) from water.

    Levchuk, Irina; Bhatnagar, Amit; Sillanpää, Mika

    2014-04-01

    Wide use of methyl tert-butyl ether (MTBE) as fuel oxygenates leads to worldwide environment contamination with this compound basically due to fuel leaks from storage or pipelines. Presence of MTBE in drinking water is of high environmental and social concern. Existing methods for MTBE removal from water have a number of limitations which can be possibly overcome in the future with use of emerging technologies. This work aims to provide an updated overview of recent developments in technologies for MTBE removal from water. Copyright © 2014. Published by Elsevier B.V.

  8. Ozone-assisted Regeneration of Magnetic Carbon Nanotubes for Removing Organic Water Pollutants

    Ateia, Mohamed; Ceccato, Marcel; Budi, Akin

    2018-01-01

    (MCNTs) after they have been used to remove organic pollutants from water. We ran MCNT through multiple regeneration cycles (i.e. magnetic collection → ozone regeneration → washing with ethanol then water) to adsorb atrazine. The results of our adsorption experiments show that the atrazine removal...... consecutive regeneration cycles. Additionally, we used a three layer graphite slab as a model system for CNTs and performed density functional theory (DFT) calculations to determine the free energy of adsorption and the free energy of solvation of atrazine and its byproducts in water and ethanol. The results...

  9. Procedure to remove a dirt and/or oil film from water

    Jager, T; Jager, G P.A.; Jager, K L.E.

    1970-12-11

    A procedure is described to remove dirt and/or oil films from a water surface. A number of rotating wiper scoops moves through the water. The top of the polluted water is brought into motion by the scoops and directed to a gutter system where it is removed. The advantage of the system is that the wiper scoops can be lowered selectively to the depth of the pollutant, thereby avoiding moving large quantities of unnecessary unpolluted liquid which later has to be separated. (12 claims)

  10. Effect of CaCO3(S) nucleation modes on algae removal from alkaline water.

    Choi, Jin Yong; Kinney, Kerry A; Katz, Lynn E

    2016-02-29

    The role of calcite heterogeneous nucleation was studied in a particle coagulation treatment process for removing microalgae from water. Batch experiments were conducted with Scenedesmus sp. and Chlorella sp. in the presence and absence of carbonate and in the presence and absence of Mg to delineate the role of CaCO 3(S) nucleation on microalgae removal. The results indicate that effective algae coagulation (e.g., up to 81 % algae removal efficiency) can be achieved via heterogeneous nucleation with CaCO 3(S) ; however, supersaturation ratios between 120 and 200 are required to achieve at least 50% algae removal, depending on ion concentrations. Algae removal was attributed to adsorption of Ca 2+ onto the cell surface which provides nucleation sites for CaCO 3(S) precipitation. Bridging of calcite particles between the algal cells led to rapid aggregation and formation of larger flocs. However, at higher supersaturation conditions, algae removal was diminished due to the dominance of homogeneous nucleation of CaCO 3(S) . Removal of algae in the presence of Ca 2+ and Mg 2+ required higher supersaturation values; however, the shift from heteronucleation to homonucleation with increasing supersaturation was still evident. The results suggest that water chemistry, pH, ionic strength, alkalinity and Ca 2+ concentration can be optimized for algae removal via coagulation-sedimentation.

  11. Combining Ferric Salt and Cactus Mucilage for Arsenic Removal from Water.

    Fox, Dawn I; Stebbins, Daniela M; Alcantar, Norma A

    2016-03-01

    New methods to remediate arsenic-contaminated water continue to be studied, particularly to fill the need for accessible methods that can significantly impact developing communities. A combination of cactus mucilage and ferric (Fe(III)) salt was investigated as a flocculation-coagulation system to remove arsenic (As) from water. As(V) solutions, ferric nitrate, and mucilage suspensions were mixed and left to stand for various periods of time. Visual and SEM observations confirmed the flocculation action of the mucilage as visible flocs formed and settled to the bottom of the tubes within 3 min. The colloidal suspensions without mucilage were stable for up to 1 week. Sample aliquots were tested for dissolved and total arsenic by ICP-MS and HGAFS. Mucilage treatment improved As removal (over Fe(III)-only treatment); the system removed 75-96% As in 30 min. At neutral pH, removal was dependent on Fe(III) and mucilage concentration and the age of the Fe(III) solution. The process is fast, achieving maximum removal in 30 min, with the majority of As removed in 10-15 min. Standard jar tests with 1000 μg/L As(III) showed that arsenic removal and settling rates were pH-dependent; As removal was between 52% (high pH) and 66% (low pH).

  12. Development of iron-based nanoparticles for Cr(VI removal from drinking water

    Vourlias G.

    2013-01-01

    Full Text Available A great deal of research over recent decades has been motivated by the requirement to lower the concentration of chromium in drinking water. This study has been conducted to determine the feasibility of iron-based nanoparticles for chromium removal from contaminated water. Single Fe, Fe3O4 and binary Fe/Fe3O4 nanoparticles were grown at the 45-80 nm size range using the solar physical vapor deposition technique and tested as potential hexavalent chromium removing agents from aqueous solutions. Due to their higher electron donation ability compared to the Fe3O4 ones, single Fe nanoparticles exhibited the highest Cr(VI removal capacity of more than 3 µg/mg while maintaining a residual concentration 50 µg/L, equal to the regulation limit for drinking water. In combination to their facile and fast magnetic separation, the applicability of the studied particles in water treatment facilities should be considered.

  13. Evaluating the Performance of Iron Nano-particle Resin in Removing Fluoride from Water

    Amir Hossein Mahvi

    2011-01-01

    Full Text Available Excessive amounts of fluoride in drinking water pose serious health problems. It is, therefore, essential to remove it from drinking water by appropriate water treatment processes down to standard levels for preventing the health risks associated. The aim of this study was to determine the performance of a kind of hybrid sorbent resin in removing fluoride from water. Batch experiments were performed to investigate adsorption isotherms and the effects of experimental parameters such as contact time (5-120 min and pH (3-9. Results revealed that fluoride adsorption rate was initially rapid but continued at a slower rate before it reached equilibrium in 120 min. Optimum fluoride removal was observed at a pH range of 3-5.5. The data obtained from the experiments were fitted with Langmiur model.

  14. Using Ultraviolet Irradiation for Removal of Malathion Pesticide in Water

    M Shayeghi

    2012-06-01

    Full Text Available Background: Organophosphorus pesticides are one of the most consumable poisons. Such poisons can enter water sources by different routes. Since consuming some drinking water containing an amount of poison higher than the standard level, causes undesirable effects on human health. This research aimed to study the effectiveness of elimi­nating malathion from water by ultraviolet irradiation (UV mercury lamp with a medium pressure.Methods: In this experimental- applied study, variants of initial pHs and initial concentrations and exposure times were investigated. Initial concentrations of malathion were 0.5, 1 and 2 mg/l. The samples were then exposed to UV irradiation interruptedly the time periods of 10, 20, 30, 40, 50 and 60 minutes. The UV lamp used in the reactor was medium pressure (irradiation intensity= 200 W/m2. The amounts of malathion were determined before and after the irradiation by HPLC instrument. Moreover, the results obtained from the study were analyzed using SPSS software and ANOVA and t-test statistical trials.Results: The minimum reduction occurs at 10 min (%46 and the maximum reduction in 60 min (% 87.25 (P< 0.05. In addition, the effectiveness of irradiation process decreases with increasing the poison concentration (P< 0.001. However, the efficiency of the process increases with pH increase.Conclusion: The results show the most effectiveness were achieved at 60 min and 0.5 mg/l and pH= 9. Therefore, the application of UV reactors could be considered as an appropriate method.

  15. Influence of the water molecules near surface of viral protein on virus activation process

    O, Shepelenko S; S, Salnikov A; V, Rak S; P, Goncharova E; B, Ryzhikov A, E-mail: shep@vector.nsc.r, E-mail: shep@ngs.r [Federal State Research Institution State Research Center of Virology and Biotechnology VECTOR of the Federal Service for Surveillance in Consumer Rights Protection and Human Well-being (FSRI SRC VB VECTOR) Koltsovo, Novosibirsk Region (Russian Federation)

    2009-06-01

    The infection of a cell with influenza virus comprises the stages of receptor binding to the cell membrane, endocytosis of virus particle, and fusion of the virus envelope and cell endosome membrane, which is determined by the conformational changes in hemagglutinin, a virus envelope protein, caused by pH decrease within the endosome. The pH value that induces conformation rearrangements of hemagglutinin molecule considerably varies for different influenza virus strains, first and foremost, due to the differences in amino acid structure of the corresponding proteins. The main goal of this study was to construct a model making it possible to assess the critical pH value characterizing the fusogenic activity of influenza virus hemagglutinin from the data on hemagglutinin structure and experimental verification of this model. Under this model, we assume that when the electrostatic force between interacting hemagglutinin molecules in the virus envelop exceeds a certain value, the hemagglutinin HA1 subunits are arranged so that they form a cavity sufficient for penetration of water molecules. This event leads to an irreversible hydration of the inner fragments of hemagglutinin molecule in a trimer and to the completion of conformational changes. The geometry of electrostatic field in hemagglutinin trimer was calculated taking into account the polarization effects near the interface of two dielectrics, aqueous medium and protein macromolecule. The critical pH values for the conformational changes in hemagglutinin were measured by the erythrocyte hemolysis induced by influenza virus particles when decreasing pH. The critical pH value conditionally separating the pH range into the regions with and without the conformational changes was calculated for several influenza virus H1N1 and H3N2 strains based on the data on the amino acid structure of the corresponding hemagglutinin molecules. Comparison of the theoretical and experimental values of critical pH values for

  16. Arsenic removal in water by means of coagulation-flocculation processes

    Franco, M. F.; Carro P, M. E.

    2014-01-01

    Arsenic and arsenical compounds are considered as carcinogenic and risky for humans according to epidemiological evidence related with the ingestion of arsenical water during a long period. In many places the only source of drinking water contains arsenic and, therefore, removal strategies have to be investigated. This work shows experimental results of coagulation-flocculation processes implemented to evaluate the efficiency in the removal of arsenic from drinking water. The main objectives include the evaluation of the relevant aspect that controls the removal efficiency. Experimental tests were performed with coagulant concentrations from 5 to 500 mg/L, solid particle concentrations from 0 to 6000 mg/L, and initial arsenic concentrations from 0.5 to 5 mg/L. These variables were simultaneously varied in more than 100 experiments. The efficiency in remediation ranged from 0% to 95%. Removal efficiency near 95% was obtained when using ferric chloride as coagulant, and was close to 80% when using aluminium sulfate as coagulant in arsenate solutions. The remediation efficiency decreased significantly when the ferric chloride concentration was higher than 50 mg/L in relation to the obtained results for aluminum sulfate for different type and concentration of soil particles. The highest removal efficiency were obtained at ph between 3 and 5 in oxidized solutions. Obtained results simulated by means of multiple linear regression analysis (R>0.90) allow determining that the main parameters that control the removal of arsenic from drinking water are coagulant concentration, ph, and solid particles concentration. Conversely, particle mineralogy and coagulant type have less significant effect on the removal by means of coagulation-flocculation mechanisms. Obtained results are relevant for the removal of As in water treatment plants as well as for the development of small scale filters. The samples were studied by scanning electron microscopy and energy dispersive X

  17. Biotreatment of produced waters for volume reduction and contaminant removal

    Negri, M.C.; Hinchman, R.R. [Argonne National Lab., IL (United States); Mollock, J. [Devon Energy Corp., Oklahoma City, OK (United States)

    1997-10-01

    Produced water is wastewater that is brought to the surface from natural gas wells during natural gas production. Its constituents, mostly salt, with traces of hydrocarbons and heavy metals, are a significant disposal problem. Argonne National Laboratory (ANL), in partnership with the Gas Research Institute (GRI), has developed a low-cost, low-tech method, in which green plants are used to reduce the volume of produced water. The authors have designed an engineered bioreactor system, which is modeled after natural saline wetland ecosystems. The plant bioreactor system maximizes plant evapotranspiration to reduce wastewater volume and, concurrently, may function as a biological filter to enhance contaminant degradation and immobilization in the root/rhizosphere zone. Halophyte plant species having high salt tolerance and high transpiration rates were selected after they tested them in greenhouse experiments. Models obtained by using their greenhouse findings reduced the volume of the wastewater (up to 6% salt) by 75% in about 8 days. A field demonstration of the bioreactor, designed on the basis of the results from the greenhouse study, is successfully under way at a natural gas well site in Oklahoma. The process could offer the petroleum industry a low-cost biological alternative to existing expensive options.

  18. Ab Initio Density Functional Theory Investigation of the Interaction between Carbon Nanotubes and Water Molecules during Water Desalination Process

    Loay A. Elalfy

    2013-01-01

    Full Text Available Density functional theory calculations using B3LYP/3-21G level of theory have been implemented on 6 carbon nanotubes (CNTs structures (3 zigzag and 3 armchair CNTs to study the energetics of the reverse osmosis during water desalination process. Calculations of the band gap, interaction energy, highest occupied molecular orbital, lowest unoccupied molecular orbital, electronegativity, hardness, and pressure of the system are discussed. The calculations showed that the water molecule that exists inside the CNT is about 2-3 Å away from its wall. The calculations have proven that the zigzag CNTs are more efficient for reverse osmosis water desalination process than armchair CNTs as the reverse osmosis process requires pressure of approximately 200 MPa for armchair CNTs, which is consistent with the values used in molecular dynamics simulations, while that needed when using zigzag CNTs was in the order of 60 MPa.

  19. The adsorption and dissociation of water molecule on goethite (010) surface: A DFT approach

    Zhou, Long, E-mail: shuweixia@ouc.edu.cn [Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, College of Chemistry and Chemical Engineering (China); Xiu, Fangyuan [Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, College of Chemistry and Chemical Engineering (China); Qiu, Meng [Qingdao Institute of Bioenergy and Bioprocess Technology (China); Xia, Shuwei; Yu, Liangmin [Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, College of Chemistry and Chemical Engineering (China)

    2017-01-15

    Graphical abstract: The optimized structure of hydrated goethite (010) surface with medium water coverage (water density about 6.7 H{sub 2}O/nm{sup 2}). - Highlights: • Stable adsorption and dissociation structure of H{sub 2}O on goethite (010) surface was investigated by DFT. • Reasonable path for water dissociation was proposed by transitional state analysis. • The mechanism of water adsorption on goethite and binding nature were revealed by PDOS. - Abstract: Using density functional theory (DFT) calculation, we investigate the configuration, stability and electronic properties of fresh cleaved (010) goethite surface (Pnma) and this surface exposed to water monolayer at low, medium and high coverage. Water is predicted to be chemisorbed to the surface, together with the surface reconstruction. The interaction energy of the most stable configuration of both low and medium coverage per water molecule is almost the same (−1.17 eV), while that of high coverage is much lower (less than 1.03 eV). It indicates that highly hydrated surface is less stable. PDOS analysis reveals the adsorption of H{sub 2}O is due to the formation of Fe−O bond, caused by overlapping of Fe's 3d and O's 2p orbitals. Dissociation processes at low and medium water coverage are non-spontaneous; while at high coverage, it can undertake spontaneously both thermodynamically and dynamically. The dissociation paths of all three water coverage are the similar. The proton from one adsorbed water is likely to dissociate to bind to the vicinal surface μ{sub 3}−O as an intermediate product; the proton belonged to μ{sub 3}−O transferred to the neighbor surface μ{sub 2}−O as the dissociative configuration.

  20. Multipole moments of water molecules in clusters and ice Ih from first principles calculations

    Batista, E.R.; Xantheas, S.S.; Jonsson, H.

    1999-01-01

    We have calculated molecular multipole moments for water molecules in clusters and in ice Ih by partitioning the charge density obtained from first principles calculations. Various schemes for dividing the electronic charge density among the water molecules were used. They include Bader close-quote s zero flux surfaces and Voronoi partitioning schemes. A comparison was also made with an induction model including dipole, dipole-quadrupole, quadrupole-quadrupole polarizability and first hyperpolarizability as well as fixed octopole and hexadecapole moments. We have found that the different density partitioning schemes lead to widely different values for the molecular multipoles, illustrating how poorly defined molecular multipoles are in clusters and condensed environments. For instance, the magnitude of the molecular dipole moment in ice Ih ranges between 2.3 D and 3.1 D depending on the partitioning scheme used. Within each scheme, though, the value for the molecular dipole moment in ice is larger than in the hexamer. The magnitude of the molecular dipole moment in the clusters shows a monotonic increase from the gas phase value to the one in ice Ih, with the molecular dipole moment in the water ring hexamer being smaller than the one in ice Ih for all the partitioning schemes used. copyright 1999 American Institute of Physics

  1. Factors influencing arsenic and nitrate removal from drinking water in a continuous flow electrocoagulation (EC) process

    Kumar, N. Sanjeev; Goel, Sudha

    2010-01-01

    An experimental study was conducted under continuous flow conditions to evaluate some of the factors influencing contaminant removal by electrocoagulation (EC). A bench-scale simulation of drinking water treatment was done by adding a filtration column after a rectangular EC reactor. Contaminant removal efficiency was determined for voltages ranging from 10 to 25 V and a comparative study was done with distilled water and tap water for two contaminants: nitrate and arsenic(V). Maximum removal efficiency was 84% for nitrate at 25 V and 75% for arsenic(V) at 20 V. No significant difference in contaminant removal was observed in tap water versus distilled water. Increase in initial As(V) concentration from 1 ppm to 2 ppm resulted in a 10% increase in removal efficiency. Turbidity in the EC reactor effluent was 52 NTU and had to be filtered to achieve acceptable levels of final turbidity (5 NTU) at steady-state. The flow regime in the continuous flow reactor was also evaluated in a tracer study to determine whether it is a plug flow reactor (PFR) or constantly stirred tank reactor (CSTR) and the results show that this reactor was close to an ideal CSTR, i.e., it was fairly well-mixed.

  2. Factors influencing arsenic and nitrate removal from drinking water in a continuous flow electrocoagulation (EC) process

    Kumar, N. Sanjeev [Civil Engineering Department, IIT Kharagpur, Kharagpur 721302 (India); Goel, Sudha, E-mail: sudhagoel@civil.iitkgp.ernet.in [Civil Engineering Department, IIT Kharagpur, Kharagpur 721302 (India)

    2010-01-15

    An experimental study was conducted under continuous flow conditions to evaluate some of the factors influencing contaminant removal by electrocoagulation (EC). A bench-scale simulation of drinking water treatment was done by adding a filtration column after a rectangular EC reactor. Contaminant removal efficiency was determined for voltages ranging from 10 to 25 V and a comparative study was done with distilled water and tap water for two contaminants: nitrate and arsenic(V). Maximum removal efficiency was 84% for nitrate at 25 V and 75% for arsenic(V) at 20 V. No significant difference in contaminant removal was observed in tap water versus distilled water. Increase in initial As(V) concentration from 1 ppm to 2 ppm resulted in a 10% increase in removal efficiency. Turbidity in the EC reactor effluent was 52 NTU and had to be filtered to achieve acceptable levels of final turbidity (5 NTU) at steady-state. The flow regime in the continuous flow reactor was also evaluated in a tracer study to determine whether it is a plug flow reactor (PFR) or constantly stirred tank reactor (CSTR) and the results show that this reactor was close to an ideal CSTR, i.e., it was fairly well-mixed.

  3. Zinc peroxide nanomaterial as an adsorbent for removal of Congo red dye from waste water.

    Chawla, Sneha; Uppal, Himani; Yadav, Mohit; Bahadur, Nupur; Singh, Nahar

    2017-01-01

    In the past decade, various natural byproducts, advanced metal oxide composites and photocatalysts have been reported for removal of dyes from water. Although these materials are useful for select applications, they have some limitations such as use at fixed temperature, ultra violet (UV) light and the need for sophisticated experimental set up. These materials can remove dyes up to a certain extent but require long time. To overcome these limitations, a promising adsorbent zinc peroxide (ZnO 2 ) nanomaterial has been developed for the removal of Congo red (CR) dye from contaminated water. ZnO 2 is highly efficient even in the absence of sunlight to remove CR from contaminated water upto the permissible limits set by the World Health Organization (WHO) and the United States- Environmental Protection Agency (US-EPA). The adsorbent has a specific property to adjust the pH of the test solution within 6.5-7.5 range irrespective of acidic or basic nature of water. The adsorption capacity of the material for CR dye was 208mgg -1 within 10min at 2-10pH range. The proposed material could be useful for the industries involved in water purification. The removal of CR has been confirmed by spectroscopic and microscopic techniques. The adsorption data followed a second order kinetics and Freundlich isotherm. Copyright © 2016 Elsevier Inc. All rights reserved.

  4. Studies on the removal of arsenic (III) from water by a novel hybrid material

    Mandal, Sandip; Padhi, T.; Patel, R.K.

    2011-01-01

    Highlights: → The removal of As (III) is about 98% at pH 7 with the hybrid material (ZrO-EA). → The hybrid material exhibits specific surface area of 201.62 m 2 /g. → The adsorption of arsenic (III) from aqueous solution by the hybrid material is spontaneous. → The material could be easily regenerated with sodium hydroxide at pH 12. - Abstract: The present work provides a method for removal of the arsenic (III) from water. An ion-exchanger hybrid material zirconium (IV) oxide-ethanolamine (ZrO-EA) is synthesized and characterized which is subsequently used for the removal of selective arsenic (III) from water containing 10,50,100 mg/L of arsenic (III) solution. The probable practical application for arsenic removal from water by this material has also been studied. The various parameters affecting the removal process like initial concentration of As (III), adsorbent dose, contact time, temperature, ionic strength, and pH are investigated. From the data of results, it is indicated that, the adsorbent dose of 0.7 mg/L, contact time 50 min after which the adsorption process comes to equilibrium, temperature (25 ± 2), solution pH (5-7), which are the optimum conditions for adsorption. The typical adsorption isotherms are calculated to know the suitability of the process. The column studies showed 98% recovery of arsenic from water especially at low concentration of arsenic in water samples.

  5. pH induced polychromatic UV treatment for the removal of a mixture of SMX, OTC and CIP from water

    Avisar, D.; Lester, Y.; Mamane, H.

    2010-01-01

    Water and wastewater effluents contain a vast range of chemicals in mixtures that have different chemical structures and characteristics. This study presents a treatment technology for the removal of mixtures of antibiotic residues (sulfamethoxazole (SMX), oxtetracycline (OTC) and ciprofloxacin (CIP)) from contaminated water. The treatment combines pH modification of the water to an optimal value, followed by a photolytic treatment using direct polychromatic ultraviolet (UV) irradiation by medium pressure UV lamp. The pH adjustment of the treated water leads to structural modifications of the pollutant's molecule thus may enhance direct photolysis by UV light. Results showed that an increase of water pH from 5 to 7 leads to a decrease in degradation rate of SMX and an increase in degradation rate of OTC and CIP, when studied separately and not in a mixture. Thus, the optimal pH values for UV photodegradation in a mixture, involve initial photolysis at pH 5 and then gradually changing the pH from 5 to 7 during the UV exposure. For example, this resulted in 99% degradation of SMX at pH 5 and enhanced degradation of OTC and CIP from 54% and 26% to 91% and 96% respectively when pH was increased from 5 to 7. Thus the pH induced photolytic treatment has a potential in improving treatment of antibiotics in mixtures.

  6. pH induced polychromatic UV treatment for the removal of a mixture of SMX, OTC and CIP from water

    Avisar, D., E-mail: droravi@post.tau.ac.il [Hydro-chemistry Laboratory, Geography and the Environment, Tel Aviv University, Tel Aviv 69978 (Israel); Lester, Y. [Hydro-chemistry Laboratory, Geography and the Environment, Tel Aviv University, Tel Aviv 69978 (Israel); School of Mechanical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv 69978 (Israel); Mamane, H. [School of Mechanical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv 69978 (Israel)

    2010-03-15

    Water and wastewater effluents contain a vast range of chemicals in mixtures that have different chemical structures and characteristics. This study presents a treatment technology for the removal of mixtures of antibiotic residues (sulfamethoxazole (SMX), oxtetracycline (OTC) and ciprofloxacin (CIP)) from contaminated water. The treatment combines pH modification of the water to an optimal value, followed by a photolytic treatment using direct polychromatic ultraviolet (UV) irradiation by medium pressure UV lamp. The pH adjustment of the treated water leads to structural modifications of the pollutant's molecule thus may enhance direct photolysis by UV light. Results showed that an increase of water pH from 5 to 7 leads to a decrease in degradation rate of SMX and an increase in degradation rate of OTC and CIP, when studied separately and not in a mixture. Thus, the optimal pH values for UV photodegradation in a mixture, involve initial photolysis at pH 5 and then gradually changing the pH from 5 to 7 during the UV exposure. For example, this resulted in 99% degradation of SMX at pH 5 and enhanced degradation of OTC and CIP from 54% and 26% to 91% and 96% respectively when pH was increased from 5 to 7. Thus the pH induced photolytic treatment has a potential in improving treatment of antibiotics in mixtures.

  7. Application of cyclodextrin nanoporous polymers in the removal of organic pollutants from water

    2009-01-01

    M.Sc. The removal of organic pollutants from industrial and municipal water is a great challenge to water providers worldwide. Some of these pollutants are very toxic and pose serious health risks to both humans and animals. Additionally, the presence of organic pollutants in the water often leads to the corrosion of turbines used for power generation at power stations. This obviously makes the power generation process less efficient and thus has cost implications, especially for the end u...

  8. Silica coated magnetite nanoparticles for removal of heavy metal ions from polluted waters

    Dash, Monika

    2013-01-01

    Magnetic removal of Hg2+ and other heavy metal ions like Cd2+, Pb2+ etc. using silica coated magnetite particles from polluted waters is a current topic of active research to provide efficient water recycling and long term high quality water. The technique used to study the bonding characteristics of such kind of nanoparticles with the heavy metal ions is a very sensitive hyperfine specroscopy technique called the perturbed angular correlation technique (PAC).

  9. An overview on the removal of synthetic dyes from water by electrochemical advanced oxidation processes.

    Nidheesh, P V; Zhou, Minghua; Oturan, Mehmet A

    2018-04-01

    Wastewater containing dyes are one of the major threats to our environment. Conventional methods are insufficient for the removal of these persistent organic pollutants. Recently much attention has been received for the oxidative removal of various organic pollutants by electrochemically generated hydroxyl radical. This review article aims to provide the recent trends in the field of various Electrochemical Advanced Oxidation Processes (EAOPs) used for removing dyes from water medium. The characteristics, fundamentals and recent advances in each processes namely anodic oxidation, electro-Fenton, peroxicoagulation, fered Fenton, anodic Fenton, photoelectro-Fenton, sonoelectro-Fenton, bioelectro-Fenton etc. have been examined in detail. These processes have great potential to destroy persistent organic pollutants in aqueous medium and most of the studies reported complete removal of dyes from water. The great capacity of these processes indicates that EAOPs constitute a promising technology for the treatment of the dye contaminated effluents. Copyright © 2018 Elsevier Ltd. All rights reserved.

  10. Nano-adsorbents for the removal of metallic pollutants from water and wastewater.

    Sharma, Y C; Srivastava, V; Singh, V K; Kaul, S N; Weng, C H

    2009-05-01

    Of the variety of adsorbents available for the removal of heavy and toxic metals, activated carbon has been the most popular. A number of minerals, clays and waste materials have been regularly used for the removal of metallic pollutants from water and industrial effluents. Recently there has been emphasis on the application of nanoparticles and nanostructured materials as efficient and viable alternatives to activated carbon. Carbon nanotubes also have been proved effective alternatives for the removal of metallic pollutants from aqueous solutions. Because of their importance from an environmental viewpoint, special emphasis has been given to the removal of the metals Cr, Cd, Hg, Zn, As, and Cu. Separation of the used nanoparticles from aqueous solutions and the health aspects of the separated nanoparticles have also been discussed. A significant number of the latest articles have been critically scanned for the present review to give a vivid picture of these exotic materials for water remediation.

  11. Pilot scale test of a produced water-treatment system for initial removal of organic compounds

    Sullivan, Enid J [Los Alamos National Laboratory; Kwon, Soondong [UT-AUSTIN; Katz, Lynn [UT-AUSTIN; Kinney, Kerry [UT-AUSTIN

    2008-01-01

    A pilot-scale test to remove polar and non-polar organics from produced water was performed at a disposal facility in Farmington NM. We used surfactant-modified zeolite (SMZ) adsorbent beds and a membrane bioreactor (MBR) in combination to reduce the organic carbon content of produced water prior to reverse osmosis (RO). Reduction of total influent organic carbon (TOC) to 5 mg/L or less is desirable for efficient RO system operation. Most water disposed at the facility is from coal-bed gas production, with oil production waters intermixed. Up to 20 gal/d of produced water was cycled through two SMZ adsorbent units to remove volatile organic compounds (BTEX, acetone) and semivolatile organic compounds (e.g., napthalene). Output water from the SMZ units was sent to the MBR for removal of the organic acid component of TOC. Removal of inorganic (Mn and Fe oxide) particulates by the SMZ system was observed. The SMZ columns removed up to 40% of the influent TOC (600 mg/L). BTEX concentrations were reduced from the initial input of 70 mg/L to 5 mg/L by the SMZ and to an average of 2 mg/L after the MBR. Removal rates of acetate (input 120-170 mg/L) and TOC (input up to 45 mg/L) were up to 100% and 92%, respectively. The water pH rose from 8.5 to 8.8 following organic acid removal in the MBR; this relatively high pH was likely responsible for observed scaling of the MBR internal membrane. Additional laboratory studies showed the scaling can be reduced by metered addition of acid to reduce the pH. Significantly, organic removal in the MBR was accomplished with a very low biomass concentration of 1 g/L throughout the field trial. An earlier engineering evaluation shows produced water treatment by the SMZ/MBR/RO system would cost from $0.13 to $0.20 per bbl at up to 40 gpm. Current estimated disposal costs for produced water are $1.75 to $4.91 per bbl when transportation costs are included, with even higher rates in some regions. Our results suggest that treatment by an SMZ

  12. Continuum Navier-Stokes modelling of water ow past fullerene molecules

    Walther, J. H.; Popadic, A.; Koumoutsakos, P.

    We present continuum simulations of water flow past fullerene molecules. The governing Navier-Stokes equations are complemented with the Navier slip boundary condition with a slip length that is extracted from related molecular dynamics simulations. We find that several quantities of interest...... as computed by the present model are in good agreement with results from atomistic and atomistic-continuum simulations at a fraction of the computational cost. We simulate the flow past a single fullerene and an array of fullerenes and demonstrate that such nanoscale flows can be computed efficiently...

  13. Continuum Navier-Stokes modelling of water flow past fullerene molecules

    Walther, J. H.; Popadic, A.; Koumoutsakos, P.

    We present continuum simulations of water flow past fullerene molecules. The governing Navier-Stokes equations are complemented with the Navier slip boundary condition with a slip length that is extracted from related molecular dynamics simulations. We find that several quantities of interest...... as computed by the present model are in good agreement with results from atomistic and atomistic-continuum simulations at a fraction of the computational cost. We simulate the flow past a single fullerene and an array of fullerenes and demonstrate that such nanoscale flows can be computed efficiently...

  14. Novel flow-through bioremediation system for removing nitrate from nursery discharge water.

    Chris Wilson, P; Albano, Joseph P

    2013-11-30

    Nitrate losses in surface runoff water from nursery production areas can be significant. This study evaluated the potential use of microbial-based (denitrification), flow-through bioreactors for their nitrate-remediation ability. Duplicate bioreactor systems were constructed at a local foliage plant nursery. Each bioreactor system consisted of four 242 L tanks with connections alternating between bottom and top. Each tank was filled with approximately 113 L of Kaldness media to provide surface area for attachment of native microflora. Molasses was supplied as a carbon source for denitrification and water flow rates through the systems ranged from 5 to 18 L min(-1) during tests. Automatic water samplers were used to collect composite samples every 15 min from both the inflow and the exit flow water. Results indicate consistent removal of 80-100% of the nitrate flowing into the systems. Accumulation of ammoniacal and nitrite nitrogen did not occur, indicating that the nitrate-nitrogen was removed from the water, and not simply transformed into another water-soluble species. Occasions where removal rates were less than 80% were usually traced to faulty delivery of the carbon source. Results indicate that modular microbial-based bioremediation systems may be a useful tool for helping water managers meet stringent nitrogen water quality regulations, especially at nurseries with limited space for expansion of water retention facilities. Copyright © 2013 Elsevier Ltd. All rights reserved.

  15. Arsenic removal from drinking water by a household sand filter in Vietnam--effect of filter usage practices on arsenic removal efficiency and microbiological water quality.

    Nitzsche, Katja Sonja; Lan, Vi Mai; Trang, Pham Thi Kim; Viet, Pham Hung; Berg, Michael; Voegelin, Andreas; Planer-Friedrich, Britta; Zahoransky, Jan; Müller, Stefanie-Katharina; Byrne, James Martin; Schröder, Christian; Behrens, Sebastian; Kappler, Andreas

    2015-01-01

    Household sand filters are applied to treat arsenic- and iron-containing anoxic groundwater that is used as drinking water in rural areas of North Vietnam. These filters immobilize poisonous arsenic (As) via co-oxidation with Fe(II) and sorption to or co-precipitation with the formed Fe(III) (oxyhydr)oxides. However, information is lacking regarding the effect of the frequency and duration of filter use as well as of filter sand replacement on the residual As concentrations in the filtered water and on the presence of potentially pathogenic bacteria in the filtered and stored water. We therefore scrutinized a household sand filter with respect to As removal efficiency and the presence of fecal indicator bacteria in treated water as a function of filter operation before and after sand replacement. Quantification of As in the filtered water showed that periods of intense daily use followed by periods of non-use and even sand replacement did not significantly (psand replacement, CFUs of Escherichia coli of sand filters regarding As removal, but indicate a potential risk for human health arising from the enrichment of coliform bacteria during filtration and from E. coli cells that are introduced by sand replacement. Copyright © 2014 Elsevier B.V. All rights reserved.

  16. Experiences on removal of sodium-water reaction products in SWAT-3

    Tanabe, H.; Hiroi, H.; Sato, M.; Otaka, J.

    2002-01-01

    This report summarizes experiences and information concerning the removal of sodium water reaction products (SMRP) obtained through large leak tests of the Steam Generator Safety Test Facility (SWAT-3) at PNC/OEC, which were conducted to validate the safety design of steam generators of a prototype LMFBR Monju. The following three problems are discussed here: (1) drainability of SWRP, (2) removal of SWRP by using a cold trap, and (3) steam cleaning of SWRP. (author)

  17. Removal of emulsified oil in residual waters by means of dissolved air flotation

    Echeverri Londono, Carlos Alberto

    1996-01-01

    In this article is consigned a theoretical and experimental study on the treatment of industrial residual waters with emulsified oil, through the flotation process for dissolved air (FAD), changing some operation parameters and some importance topics, related with the process. The experimental results and the theoretical pattern, show that the removal of oil depends fundamentally on the chemical pretreatment. Efficiencies of removal of oil up of 99% they were obtained, using the dissolved air flotation with the help of coagulants

  18. An innovative bovine odorant binding protein-based filtering cartridge for the removal of triazine herbicides from water.

    Bianchi, Federica; Basini, Giuseppina; Grolli, Stefano; Conti, Virna; Bianchi, Francesco; Grasselli, Francesca; Careri, Maria; Ramoni, Roberto

    2013-01-01

    Odorant binding protein (OBP) is a multi-functional scavenger for small hydrophobic molecules dissolved in the mucus lining the nasal epithelia of mammals, characterized by broad ligand binding specificity towards a large number of structurally unrelated natural and synthetic molecules of different chemical classes. Here, we demonstrate for the first time the application of OBP as the active element of an innovative filtering matrix for the removal of environmental pollutants such as triazine herbicides from water samples. The filtering device, obtained by coupling histidine-tagged bovine OBP to a nickel nitrilotriacetic acid (Ni-NTA) agarose resin, was characterized in terms of retention capacity for the herbicides atrazine, simazine, and propazine. Analysis of these herbicides at trace levels with solid-phase microextraction followed by gas chromatography-mass spectrometry using the selected ion monitoring mode proved the capabilities of the proposed device for the decontamination of surface and groundwater samples in the 0.2-2,300 μg/L concentration range, obtaining a reduction in the triazine content greater than 97 %, thus suggesting its possible use for the potabilization of water.

  19. Investigation of the Effect of Water Removal from Wells Surrounding Parishan Lake on Groundwater and Surface Water Levels

    Shafiei, M.; Raini Sarjaz, M.; Fazloli, R.; Gholami Sefidkouhi, M. A.

    2017-01-01

    In recent decades the human impacts on global warming and, its consequences, climate change, stirred up earth ecosystems balance and has created many problems all over the world. Unauthorized underground water removal, especially in arid and semi-arid regions of Iran, along with recent decade drought occurrences significantly lowered underground and surface water levels. To investigate the impacts of water removal from surrounding wells in Parishan Lake water level, during 1996 to 2009 interval, 8 buffer layers surrounding the lake were mapped in ArcGIS 9.3 environment. Each buffer layer wells and their total annual discharges were determined. Using SPSS 16 software, the regression equations between wells water levels and water discharges were computed. By employing Thiessen function and creating Thiessen network (TIN) around observation wells, decline of groundwater levels was evaluated. Finally regression equations between wells discharges and groundwater level declines were created. The findings showed that there are highly significant correlations (p ≤ 0.01), in all buffer layers, between water levels and wells discharges. Investigation of the observation wells surrounding lake showed that severe groundwater level declines has been started since the beginning of the first decade of the 21st century. Using satellite images in ArcGIS 9.3 environment it was confirmed that lake’s area has been reduced significantly. In conclusion, it is obvious that human interferences on lake’s natural ecosystem by digging unauthorized wells and removing underground water more than annual recharges significantly impacted surface and groundwater levels.

  20. Explicit Consideration of Water Molecules to Study Vibrational Circular DICHROÎSM of Monosaccharide's

    Moussi, Sofiane; Ouamerali, Ourida

    2014-06-01

    Carbohydrates have multiples roles in biological systems. It has been found that the glycoside bond is fundamentally important in many aspects of chemistry and biology and forms the basis of carbohydrate chemistry. That means the stereochemical information, namely, glycosidic linkages α or β, gives an significant features of the carbohydrate glycosidation position of the glycosylic acceptor. For these reasons, much effort was made for the synthesis and analysis of the glycoside bond. Vibrational circular dichroism VCD has some advantages over conventional electronic circular dichroism (ECD) due to the applicability to all organic molecules and the reliability of ab initio quantum calculation. However, for a molecule with many chiral centers such as carbohydrates, determination of the absolute configuration tends to be difficult because the information from each stereochemical center is mixed and averaged over the spectrum. In the CH stretching region, only two VCD studies on carbohydrates have been reported and spectra--structure correlation, as determined for the glycoside band, remains to be investigated. T. Taniguchi and collaborators report that methyl glycosides exhibit a characteristic VCD peak, the sign of which solely reflects the C-1 absolute configuration. This work is a theoretical contribution to study the behaviour of VCD spectrum's of the monosaccharides when the water molecules are taken explicitly. This study is focused on six different monosaccharides in theirs absolute configuration R and S. We used the method of density functional theory DFT by means of the B3LYP hybrid functional and 6-31G * basis set.

  1. Biological nitrate removal processes from drinking water supply-a review.

    Mohseni-Bandpi, Anoushiravan; Elliott, David Jack; Zazouli, Mohammad Ali

    2013-12-19

    This paper reviews both heterotrophic and autotrophic processes for the removal of nitrate from water supplies. The most commonly used carbon sources in heterotrophic denitrification are methanol, ethanol and acetic acid. Process performance for each feed stock is compared with particular reference nitrate and nitrite residual and to toxicity potential. Autotrophic nitrate removal has the advantages of not requiring an organic carbon source; however the slow growth rate of autotrophic bacteria and low nitrate removal rate have contributed to the fact that relatively few full scale plants are in operation at the present time.

  2. Removal of benzaldehyde from a water/ethanol mixture by applying scavenging techniques

    Mitic, Aleksandar; Skov, Thomas; Gernaey, Krist V.

    2017-01-01

    A presence of carbonyl compounds is very common in the food industry. The nature of such compounds is to be reactive and thus many products involve aldehydes/ketones in their synthetic routes. By contrast, the high reactivity of carbonyl compounds could also lead to formation of undesired compounds......, such as genotoxic impurities. It can therefore be important to remove carbonyl compounds by implementing suitable removal techniques, with the aim of protecting final product quality. This work is focused on benzaldehyde as a model component, studying its removal from a water/ethanol mixture by applying different...

  3. Nanofiltration vs. reverse osmosis for the removal of emerging organic contaminants in water reuse

    Yangali-Quintanilla, Victor

    2011-01-01

    Reverse osmosis (RO) in existing water reuse facilities is a water industry standard. However, that approach may be questioned taking into consideration that "tight" NF can be equal or "better" than RO. NF can achieve the same removals of RO membranes when dealing with emerging organic contaminants (pharmaceuticals, pesticides, endocrine disruptors and others). Experiments using 18 emerging contaminants were performed using membranes NF200 and NF90 at bench-scale units, and for a more complete study, results of NF and RO pilot and fullscale experiments where compared to our experimental results. The removal results showed that NF can remove many emerging contaminants. The average removal by tight NF was 82% for neutral contaminants and 97% for ionic contaminants. The average removal by RO was 85% for neutral contaminants and 99% for ionic contaminants. Aquifer recharge and recovery (ARR) followed by NF can effectively remove emerging contaminants with removals over 90% when loose NF membranes are used. © 2011 2011 Desalination Publications. All rights reserved.

  4. Study of the Efficiency of Arsenic Removal from Drinking Water by Granular Ferric Hydroxide (GFH

    .R. Asgari

    2008-04-01

    Full Text Available Background and ObjectivePollution of surface and ground water to arsenic (As has been reported from many parts of the world and in some regions of Iran especially in Kurdistan province. Natural pollution of water to As is in fact dependent to geological characteristics of a region. To day, various methods have been recommended for As removal that each of which has special advantages and drawbacks. Granular ferric hydroxide (GFH is a relatively new adsorbent available in market which is principally introduced for As removal.MethodsThis study was an applied survey in which the effects of changing contact time, As concentration, adsorbent weight, pH as well as the effect of sulfate and chloride ions in arsenic removal were determined. Moreover, the model of absorption by GFH was studied and compared with Freundlich and Langmuir models. Raw data were analyzed by Excel and SPSS softwares. ResultsResults showed that As adsorption by GFH imitate both the Freundlich and Langmuir equations (with R2 >0.95. Optimum PH was 7.5 and duration of the process about 30 minutes was sufficient for optimum removal of As. It was also found that efficiency of As removal was high when small amounts of adsorbent were used. Furthermore, sulfate and chloride ions in concentrations used in this study had no noticeable effect on As removal and Fe added during process remains in the water more than the standard value (0.3 mg/l.ConclusionAccording to this study, GFH could be considered as a suitable adsorbent for As removal from polluted water resources because of its high performance without any needs to PH adjustment. However, there are few drawbacks such as Fe addition and relatively high initial cost. Keywords: Arsenic, Granular Ferric Hydroxide (GFH, Adsorption, Drinking Water

  5. Occurrence of illicit drugs in water and wastewater and their removal during wastewater treatment.

    Yadav, Meena K; Short, Michael D; Aryal, Rupak; Gerber, Cobus; van den Akker, Ben; Saint, Christopher P

    2017-11-01

    This review critically evaluates the types and concentrations of key illicit drugs (cocaine, amphetamines, cannabinoids, opioids and their metabolites) found in wastewater, surface water and drinking water sources worldwide and what is known on the effectiveness of wastewater treatment in removing such compounds. It is also important to amass information on the trends in specific drug use as well as the sources of such compounds that enter the environment and we review current international knowledge on this. There are regional differences in the types and quantities of illicit drug consumption and this is reflected in the quantities detected in water. Generally, the levels of illicit drugs in wastewater effluents are lower than in raw influent, indicating that the majority of compounds can be at least partially removed by conventional treatment processes such as activated sludge or trickling filters. However, the literature also indicates that it is too simplistic to assume non-detection equates to drug removal and/or mitigation of associated risks, as there is evidence that some compounds may avoid detection via inadequate sampling and/or analysis protocols, or through conversion to transformation products. Partitioning of drugs from the water to the solids fraction (sludge/biosolids) may also simply shift the potential risk burden to a different environmental compartment and the review found no information on drug stability and persistence in biosolids. Generally speaking, activated sludge-type processes appear to offer better removal efficacy across a range of substances, but the lack of detail in many studies makes it difficult to comment on the most effective process configurations and operations. There is also a paucity of information on the removal effectiveness of alternative treatment processes. Research is also required on natural removal processes in both water and sediments that may over time facilitate further removal of these compounds in receiving

  6. Nitrate removal from drinking water with a focus on biological methods: a review.

    Rezvani, Fariba; Sarrafzadeh, Mohammad-Hossein; Ebrahimi, Sirous; Oh, Hee-Mock

    2017-05-31

    This article summarizes several developed and industrial technologies for nitrate removal from drinking water, including physicochemical and biological techniques, with a focus on autotrophic nitrate removal. Approaches are primarily classified into separation-based and elimination-based methods according to the fate of the nitrate in water treatment. Biological denitrification as a cost-effective and promising method of biological nitrate elimination is reviewed in terms of its removal process, applicability, efficiency, and associated disadvantages. The various pathways during biological nitrate removal, including assimilatory and dissimilatory nitrate reduction, are also explained. A comparative study was carried out to provide a better understanding of the advantages and disadvantages of autotrophic and heterotrophic denitrification. Sulfur-based and hydrogen-based denitrifications, which are the most common autotrophic processes of nitrate removal, are reviewed with the aim of presenting the salient features of hydrogenotrophic denitrification along with some drawbacks of the technology and research areas in which it could be used but currently is not. The application of algae-based water treatment is also introduced as a nature-inspired approach that may broaden future horizons of nitrate removal technology.

  7. THE EFFICIENCY OF ELECTROCOAGULATION PROCESS USING ALUMINUM ELECTRODES IN REMOVAL OF HARDNESS FROM WATER

    M. Malakootian ، N. Yousefi

    2009-04-01

    Full Text Available There are various techniques for removal of water hardness each with its own special advantages and disadvantages. Electrochemical or electrocoagulation method due to its simplicity has gained a great attention and is used for removal of various ions and organic matters. The aim of the present study was to investigate the efficiency of this technique in removal of water hardness under different conditions. This experimental study was performed using a pilot plant. The applied pilot was comprised of a reservoir containing aluminum sheet electrodes. The electrodes were connected as monopolar and a power supply was used for supplying direct electrical current. Drinking water of Kerman (southeast of Iran was used in the experiments. The efficiency of the system in three different pH, voltages and time intervals were determined. Results showed the efficiency of 95.6% for electrocoagulation technique in hardness removal. pH and electrical potential had direct effect on hardness removal in a way that the highest efficiency rate was obtained in pH=10.1, potential difference of 20 volt and detention time of 60 minutes. Considering the obtained efficiency in the present study, electrocoagulation technique may be suggested as an effective alternative technique in hardness removal.

  8. Potential of duckweed (Lemna minor) for removal of nitrogen and phosphorus from water under salt stress.

    Liu, Chunguang; Dai, Zheng; Sun, Hongwen

    2017-02-01

    Duckweed plays a major role in the removal of nitrogen (N) and phosphorus (P) from water. To determine the effect of salt stress on the removal of N and P by duckweed, we cultured Lemna minor, a common species of duckweed, in N and P-rich water with NaCl concentrations ranging from 0 to 100 mM for 24 h and 72 h, respectively. The results show that the removal capacity of duckweed for N and P was reduced by salt stress. Higher salt stress with longer cultivation period exerts more injury to duckweed and greater inhibition of N and P removal. Severe salt stress (100 mM NaCl) induced duckweed to release N and P and even resulted in negative removal efficiencies. The results indicate that L. minor should be used to remove N and P from water with salinities below 75 mM NaCl, or equivalent salt stress. Copyright © 2016 Elsevier Ltd. All rights reserved.

  9. Removal of bacteria and viruses from waters using layered double hydroxide nanocomposites

    Song Jin et al

    2007-01-01

    Full Text Available We have identified synthetic layered double hydroxides (LDH nanocomposites as an effective group of material for removing bacteria and viruses from water. In this study, LDH nanocomposites were synthesized and tested for removing biological contaminants. LDH was used to remove MS2 and X174 (indicator viruses, and Escherichia coli (an indicator bacterium from synthetic groundwater and to remove mixed communities of heterotrophic bacteria from raw river water. Our results indicate that LDH composed of magnesium–aluminium or zinc–aluminium has a viral and bacterial adsorption efficiency ≥99% at viral concentrations between 5.9×106 and 9.1×106 plaque forming units (pfu/L and bacterial concentrations between 1.6×1010 and 2.6×1010 colony forming units (cfu/L when exposed to LDH in a slurry suspension system. Adsorption densities of viruses and bacteria to LDH in suspension ranged from 1.4×1010 to 2.1×1010 pfu/kg LDH and 3.2×1013–5.2×1013 cfu/kg LDH, respectively. We also tested the efficiency of LDH in removing heterotrophic bacteria from raw river water. While removal efficiencies were still high (87–99%, the adsorption capacities of the two kinds of LDH were 4–5 orders of magnitude lower than when exposed to synthetic groundwater, depending on if the LDH was in suspension or a packed column, respectively.

  10. Nutrient removal from Chinese coastal waters by large-scale seaweed aquaculture

    Xiao, Xi; Agusti, Susana; Lin, Fang; Li, Ke; Pan, Yaoru; Yu, Yan; Zheng, Yuhan; Wu, Jiaping; Duarte, Carlos M.

    2017-01-01

    China is facing intense coastal eutrophication. Large-scale seaweed aquaculture in China is popular, now accounting for over 2/3's of global production. Here, we estimate the nutrient removal capability of large-scale Chinese seaweed farms to determine its significance in mitigating eutrophication. We combined estimates of yield and nutrient concentration of Chinese seaweed aquaculture to quantify that one hectare of seaweed aquaculture removes the equivalent nutrient inputs entering 17.8 ha for nitrogen and 126.7 ha for phosphorus of Chinese coastal waters, respectively. Chinese seaweed aquaculture annually removes approximately 75,000 t nitrogen and 9,500 t phosphorus. Whereas removal of the total N inputs to Chinese coastal waters requires a seaweed farming area 17 times larger than the extant area, one and a half times more of the seaweed area would be able to remove close to 100% of the P inputs. With the current growth rate of seaweed aquaculture, we project this industry will remove 100% of the current phosphorus inputs to Chinese coastal waters by 2026. Hence, seaweed aquaculture already plays a hitherto unrealized role in mitigating coastal eutrophication, a role that may be greatly expanded with future growth of seaweed aquaculture.

  11. Nutrient removal from Chinese coastal waters by large-scale seaweed aquaculture

    Xiao, Xi

    2017-04-21

    China is facing intense coastal eutrophication. Large-scale seaweed aquaculture in China is popular, now accounting for over 2/3\\'s of global production. Here, we estimate the nutrient removal capability of large-scale Chinese seaweed farms to determine its significance in mitigating eutrophication. We combined estimates of yield and nutrient concentration of Chinese seaweed aquaculture to quantify that one hectare of seaweed aquaculture removes the equivalent nutrient inputs entering 17.8 ha for nitrogen and 126.7 ha for phosphorus of Chinese coastal waters, respectively. Chinese seaweed aquaculture annually removes approximately 75,000 t nitrogen and 9,500 t phosphorus. Whereas removal of the total N inputs to Chinese coastal waters requires a seaweed farming area 17 times larger than the extant area, one and a half times more of the seaweed area would be able to remove close to 100% of the P inputs. With the current growth rate of seaweed aquaculture, we project this industry will remove 100% of the current phosphorus inputs to Chinese coastal waters by 2026. Hence, seaweed aquaculture already plays a hitherto unrealized role in mitigating coastal eutrophication, a role that may be greatly expanded with future growth of seaweed aquaculture.

  12. Electrochemical filtration for turbidity removal in industrial cooling/process water systems

    Kumbhar, A.G.; Venkateswaran, G.

    2008-01-01

    Water samples of large cooling water reservoirs may look visibly clear and transparent, but still may contain sub-micron size particles at sub-parts-per-million levels. Deposition of these particles on heat exchanger surfaces, reduces the heat transfer efficiency in power industry. In nuclear power plants, additionally it creates radiation exposure problems due to activation of fine metallic turbidity in the reactor core and its subsequent transfer to out-of-core surfaces. Sub-micron filtration creates back high-pressure problem. Zeta filters available commercially are prescribed for separating either positively or negatively charged particles. They are of once-use and throw-type. Precipitation surface modified ion exchangers impart chemical impurities to the system. Thus, sub-micron size and dilute turbidity removal from large volumes of waters such as heat exchanger cooling water in nuclear and power industry poses a problem. Electro deposition of the turbidity causing particles, on porous carbon/graphite felt electrodes, is one of the best suited methods for turbidity removal from large volumes of water due to the filter's high permeability, inertness to the system and regenerability resulting in low waste generation. Initially, active indium turbidity removal from RAPS-1 heavy water moderator system, and microbes removal from heat exchanger cooling lake water of RAPS 1 and 2 were demonstrated with in-house designed and fabricated prototype electrochemical filter (ECF). Subsequently, a larger size, high flow filter was fabricated and deployed for iron turbidity removal from active process waters system of Kaiga Generation Station unit 1 and silica and iron turbidity removal from cooling water pond used for heat exchanger of a high temperature high pressure (HTHP) loop at WSCD, Kalpakkam. The ECF proved its exclusive utility for sub-micron size turbidity removal and microbes removal. ECF maneuverability with potential and current for both positively and

  13. Using Magnetically Responsive Tea Waste to Remove Lead in Waters under Environmentally Relevant Conditions

    Yeo, Siang Yee; Choi, Siwon; Dien, Vivian; Sow-Peh, Yoke Keow; Qi, Genggeng; Hatton, T. Alan; Doyle, Patrick S.; Thio, Beng Joo Reginald

    2013-01-01

    We report the use of a simple yet highly effective magnetite-waste tea composite to remove lead(II) (Pb2+) ions from water. Magnetite-waste tea composites were dispersed in four different types of water–deionized (DI), artificial rainwater, artificial groundwater and artificial freshwater–that mimic actual environmental conditions. The water samples had varying initial concentrations (0.16–5.55 ppm) of Pb2+ ions and were mixed with the magnetite-waste tea composite for at least 24 hours to allow adsorption of the Pb2+ ions to reach equilibrium. The magnetite-waste tea composites were stable in all the water samples for at least 3 months and could be easily removed from the aqueous media via the use of permanent magnets. We detected no significant leaching of iron (Fe) ions into the water from the magnetite-waste tea composites. The percentage of Pb adsorbed onto the magnetite-waste tea composite ranged from ~70% to 100%; the composites were as effective as activated carbon (AC) in removing the Pb2+ ions from water, depending on the initial Pb concentration. Our prepared magnetite-waste tea composites show promise as a green, inexpensive and highly effective sorbent for removal of Pb in water under environmentally realistic conditions.

  14. Performance of Electrocoagulation Process in the Removal of Total Coliform and Hetrotrophic Bacteria from Surface Water

    Jamshid Derayat

    2015-03-01

    Full Text Available Electrocoagulation is an electrochemical method for the treatment of water and wastewater. The present cross-sectional study was designed to investigate the removal efficiency of total coliform and heterotrophic bacteria from surface water using the process. For this purpose, water samples were taken from the drinking water intake at Suleiman-Shahsonghur Dam. The electrocoagulation process was carried out in a Plexiglas reactor in the batch mode with Al and Fe used electrodes. The experiment design was carried out using the Design Expert Software (Stat-Ease Inc., Ver. 6.0.6. After each run, the values of metals dissolved due to anode electrode dissolution were measured using the Inductively Coupled Plasma (ICP and the results were analyzed using the RSM model. Results revealed maximum removal efficiencies of 100% and 89.1% for total coliform and heterotrophic bacteria using the Al electrode, respectively. Also, maximum removal efficiencies using the Fe electrode for the same pollutants were 100% and 76.1%. The measurements clearly indicate that the quantities of Al and Fe released in water were higher than the recommended values. While the electrocoagulation process showed to be effective in removing microbial agents from surface waters, the high concentrations of dissolved metals due to the dissolution of the anode electrode seem to remain a health problem that requires optimal conditions to be determined for acheiving standard concentrations of the dissolved metals.

  15. Removal of Water-Soluble Extractives Improves the Enzymatic Digestibility of Steam-Pretreated Softwood Barks.

    Frankó, Balázs; Carlqvist, Karin; Galbe, Mats; Lidén, Gunnar; Wallberg, Ola

    2018-02-01

    Softwood bark contains a large amounts of extractives-i.e., soluble lipophilic (such as resin acids) and hydrophilic components (phenolic compounds, stilbenes). The effects of the partial removal of water-soluble extractives before acid-catalyzed steam pretreatment on enzymatic digestibility were assessed for two softwood barks-Norway spruce and Scots pine. A simple hot water extraction step removed more than half of the water-soluble extractives from the barks, which improved the enzymatic digestibility of both steam-pretreated materials. This effect was more pronounced for the spruce than the pine bark, as evidenced by the 30 and 11% glucose yield improvement, respectively, in the enzymatic digestibility. Furthermore, analysis of the chemical composition showed that the acid-insoluble lignin content of the pretreated materials decreased when water-soluble extractives were removed prior to steam pretreatment. This can be explained by a decreased formation of water-insoluble "pseudo-lignin" from water-soluble bark phenolics during the acid-catalyzed pretreatment, which otherwise results in distorted lignin analysis and may also contribute to the impaired enzymatic digestibility of the barks. Thus, this study advocates the removal of extractives as the first step in the processing of bark or bark-rich materials in a sugar platform biorefinery.

  16. Using Magnetically Responsive Tea Waste to Remove Lead in Waters under Environmentally Relevant Conditions

    Yeo, Siang Yee

    2013-06-20

    We report the use of a simple yet highly effective magnetite-waste tea composite to remove lead(II) (Pb2+) ions from water. Magnetite-waste tea composites were dispersed in four different types of water–deionized (DI), artificial rainwater, artificial groundwater and artificial freshwater–that mimic actual environmental conditions. The water samples had varying initial concentrations (0.16–5.55 ppm) of Pb2+ ions and were mixed with the magnetite-waste tea composite for at least 24 hours to allow adsorption of the Pb2+ ions to reach equilibrium. The magnetite-waste tea composites were stable in all the water samples for at least 3 months and could be easily removed from the aqueous media via the use of permanent magnets. We detected no significant leaching of iron (Fe) ions into the water from the magnetite-waste tea composites. The percentage of Pb adsorbed onto the magnetite-waste tea composite ranged from ~70% to 100%; the composites were as effective as activated carbon (AC) in removing the Pb2+ ions from water, depending on the initial Pb concentration. Our prepared magnetite-waste tea composites show promise as a green, inexpensive and highly effective sorbent for removal of Pb in water under environmentally realistic conditions.

  17. Improvement of NOM Removal from Water Resources by Modifying the Coagulation Process

    F Vaezi, A Mohagheghian, J Nouri, MR Eshraghian, A Ghasri

    2005-01-01

    Full Text Available As a result of the regulations on DBPs, interest in NOM removal is increasing and many water treatment plants in developed countries have started to measure the concentration of TOC in their finished waters. Promulgation of the rules will substantially increase these efforts in other countries too. Since the cost of TOC (and DBPs determination was high, it was decided to study the traditional analysis of COD as a surrogate measure to detect the organic constituents in raw water and the extent to which optimized coagulation with ferric chloride can increase COD removal. The two water samples studied belonged to Karaj and Jajrood Rivers. For both samples the observed values of COD removal by coagulation at lower pH (about 1-1.5 pH values less than the regular pH were about 85-95 percent without making water turbidity unacceptable. In order to determine the effects of organic content on coagulation, synthetic samples were also prepared with much higher COD values. Again, considerable increases in COD removal have been observed for most of these samples only by decreasing 0.5-2 pH value. The results indicated that a modified coagulation process without need to much increasing the amount of coagulant can be developed for these water samples.

  18. Winter Maintenance Wash-Water Heavy Metal Removal Pilot Scale Evaluation

    Christopher M. Miller

    2016-01-01

    Full Text Available To encourage sustainable engineering practices, departments of transportation are interested in reusing winter maintenance truck wash water as part of their brine production and future road application. Traffic-related metals in the wash water, however, could limit this option. The objective of this work was to conduct a pilot scale evaluation of heavy metal (copper, zinc, iron, and lead removal in a filtration unit (maximum flow rate of 45 L/minute containing proprietary (MAR Systems Sorbster® media. Three different trials were conducted and approximately 10,000 L of wash water collected from a winter maintenance facility in Ohio was treated with the pilot unit. Lab studies were also performed on six wash-water samples from multiple facilities to assess particle size removal and estimate settling time as a potential removal mechanism during wash-water storage. Pilot unit total metal removal efficiencies were 79%, 77%, 63%, and 94% for copper, zinc, iron, and lead, respectively. Particle settling calculation estimates for copper and zinc show that 10 hours in storage can also effectively reduce heavy metal concentrations in winter maintenance wash water in excess of 70%. These pilot scale results show promise for reducing heavy metal concentrations to an acceptable level for reuse.

  19. The removal of uranium from mining waste water using algal/microbial biomass

    Kalin, Margarete; Wheeler, W.N.; Meinrath, G.

    2004-01-01

    We describe a three step process for the removal of uranium (U) from dilute waste waters. Step one involves the sequestration of U on, in, and around aquatic plants such as algae. Cell wall ligands efficiently remove U(VI) from waste water. Growing algae continuously renew the cellular surface area. Step 2 is the removal of U-algal particulates from the water column to the sediments. Step 3 involves reducing U(VI) to U(IV) and transforming the ions into stable precipitates in the sediments. The algal cells provide organic carbon and other nutrients to heterotrophic microbial consortia to maintain the low E H , within which the U is transformed. Among the microorganisms, algae are of predominant interest for the ecological engineer because of their ability to sequester U and because some algae can live under many extreme environments, often in abundance. Algae grow in a wide spectrum of water qualities, from alkaline environments (Chara, Nitella) to acidic mine drainage waste waters (Mougeotia, Ulothrix). If they could be induced to grow in waste waters, they would provide a simple, long-term means to remove U and other radionuclides from U mining effluents. This paper reviews the literature on algal and microbial adsorption, reduction, and transformation of U in waste streams, wetlands, lakes and oceans

  20. Magnetite nanoparticles coated glass wool for As(V) removal from drinking water

    Kango, Sarita; Kumar, Rajesh, E-mail: rajesh.kumar@juit.ac.in [Department of Physics and Materials Science, Jaypee University of Information Technology, Waknaghat, District Solan (H.P.)- 173 234 (India)

    2015-08-28

    Arsenic (As) removal from contaminated groundwater is a key environmental concern worldwide. In this study, glass wool was coated with magnetite nanoparticles under argon gas flow and magnetite coated glass wool have been investigated for application as an adsorbent for As(V) removal from water. The adsorbent was characterized by using Scanning Electron Microscopy (SEM) and arsenic contaminated water treated with adsorbent was analyzed by Inductively Coupled Plasma Mass Spectroscopy (ICP-MS). The ICP-MS results showed that 10 g/L of adsorbent removed 99.4% of As(V) within 5 hours at pH-7 and initial arsenic concentration of 360µg/L. Adsorption kinetics data fitted well in pseudo-first-order kinetics model with high correlation coefficient (R{sup 2} = 0.995). As magnetite nanoparticles coated glass wool showed favorable adsorption behavior for As(V), it can be a promising tool for water purification.

  1. Magnetite nanoparticles coated glass wool for As(V) removal from drinking water

    Kango, Sarita; Kumar, Rajesh

    2015-01-01

    Arsenic (As) removal from contaminated groundwater is a key environmental concern worldwide. In this study, glass wool was coated with magnetite nanoparticles under argon gas flow and magnetite coated glass wool have been investigated for application as an adsorbent for As(V) removal from water. The adsorbent was characterized by using Scanning Electron Microscopy (SEM) and arsenic contaminated water treated with adsorbent was analyzed by Inductively Coupled Plasma Mass Spectroscopy (ICP-MS). The ICP-MS results showed that 10 g/L of adsorbent removed 99.4% of As(V) within 5 hours at pH-7 and initial arsenic concentration of 360µg/L. Adsorption kinetics data fitted well in pseudo-first-order kinetics model with high correlation coefficient (R 2 = 0.995). As magnetite nanoparticles coated glass wool showed favorable adsorption behavior for As(V), it can be a promising tool for water purification

  2. Removal of NO and SO2 in Corona Discharge Plasma Reactor with Water Film

    贺元吉; 董丽敏; 杨嘉祥

    2004-01-01

    In this paper, a novel type of a corona discharge plasma reactor was designed, which consists of needle-plate-combined electrodes, in which a series of needle electrodes are placed in a glass container filled with flue gas, and a plate electrode is immersed in the water. Based on this model, the removal of NO and SO2 was tested experimentally. In addition, the effect of streamer polarity on the reduction of SO2 and NO was investigated in detail. The experimental results show that the corona wind formed between the high-voltage needle electrode and the water by corona discharge enhances the cleaning efficiency of the flue gas because of the presence of water,and the cleaning efficiency will increase with the increase of applied dc voltage within a definite range. The removal efficiency of SO2 up to 98%, and about 85% of NOx removal under suitable conditions is obtained in our experiments.

  3. Removal of arsenic species from drinking water by Iranian natural and synthetic zeolites

    Menhaje-Bena, R.; Kazemian, H.; Shahtaheri, S.J.; Ghazi-Khansari, M.

    2003-01-01

    The main objective of this study was to find a relatively inexpensive method for removal of arsenic species from drinking water. The uptake capability of Iron (II) modified natural clinoptilolites and relevant synthetic zeolites A and P was investigated toward inorganic arsenic species from drinking water. Results obtained from sorption experiments, using a batch (static) technique showed that, among the investigated zeolites, modified synthetic zeolite A was the most selective sorbent for removal of arsenate and arsenite from drinking water. Through this study the influencing of factories including temperature, concentration, pH, particle size and interferences was evaluated on removal of arsenic species. The synthetic zeolites and their modified forms were also characterized, using XRD, XRF and thermal analysis techniques. (authors)

  4. Removal of Natural Organic Matter from Two Types of Humic Ground Waters by Nanofiltration

    Alborzfar, Maryam; Jonsson, Gunnar Eigil; Grøn, Christian

    1998-01-01

    and inorganic water chemistry types. Accumulated NOM was removed with an alkaline detergent recovering the initial membrane productivity by 90%, whereas the inorganic precipitation was removed with an acidic detergent followed by the alkaline detergent, recovering the initial productivity completely. A spiral......) of 200-500 D and a feed spacer of 0.75 mm in diamond configuration demonstrated superior NOM removal for both waters. Membrane productivity decline was observed due to the accumulation of NOM on the membrane surface or the precipitation of inorganic salts such as calcite (CaCO3), dependent upon NOM...... wound NF membrane with a nominal MWCO of 180 D and a feed spacer of 1.25 mm in parallel configuration exhibited the same product water quality, but a higher and more stable membrane productivity than the first membrane. High cross flow and low operating pressure reduced the membrane productivity decline...

  5. Preparation and characterisation of core-shell CNTs@MIPs nanocomposites and selective removal of estrone from water samples.

    Gao, Ruixia; Su, Xiaoqian; He, Xiwen; Chen, Langxing; Zhang, Yukui

    2011-01-15

    This paper reports the preparation of carbon nanotubes (CNTs) functionalized with molecularly imprinted polymers (MIPs) for advanced removal of estrone. CNTs@Est-MIPs nanocomposites with a well-defined core-shell structure were obtained using a semi-covalent imprinting strategy, which employed a thermally reversible covalent bond at the surface of silica-coated CNTs for a large-scale production. The morphology and structure of the products were characterised by transmission electron microscopy and Fourier transform infrared spectroscopy. The adsorption properties were demonstrated by equilibrium rebinding experiments and Scatchard analysis. The results demonstrate that the imprinted nanocomposites possess favourable selectivity, high capacity and fast kinetics for template molecule uptake, yielding an adsorption capacity of 113.5 μmol/g. The synthetic process is quite simple, and the different batches of synthesized CNTs@Est-MIPs nanocomposites showed good reproducibility in template binding. The feasibility of removing estrogenic compounds from environmental water using the CNTs@Est-MIPs nanocomposites was demonstrated using water samples spiked with estrone. Copyright © 2010 Elsevier B.V. All rights reserved.

  6. REMOVAL OF NATURAL ORGANIC MATTER USING ELECTROCOAGULATION AS A FIRST STEP FOR DESALINATION OF BRACKISH WATER

    Wasinton Simanjuntak

    2011-07-01

    Full Text Available In the present study, electrocoagulation method was employed to remove natural organic matter from brackish water. This study explores the potential of brackish water as a source of potable water. Two electrochemical variables, potential and contact time, were tested to determine their effect on the treatment efficiency defined in terms of the reduction of the absorbance at the wavelength of 254 nm (A254. Both potential and contact time were found to influence the removal efficiency of the method, and the best result was obtained from the experiment using the potential of 8 V and contact time of 60 min, resulting in 69.5% reduction of the absorbance. Very clean treated water was produced with much lower conductivity (12.06 mS/cm as compared to that obtained for the sea water sample from a location near to the sampling site (133.9 mS/cm.

  7. An innovative carbonate coprecipitation process for the removal of zinc and manganese from mining impacted waters

    Sibrell, P.L.; Chambers, M.A.; Deaguero, A.L.; Wildeman, T.R.; Reisman, D.J.

    2007-01-01

    Although mine drainage is usually thought of as acidic, there are many cases where the water is of neutral pH, but still contains metal species that can be harmful to human or aquatic animal health, such as manganese (Mn) and zinc (Zn). Typical treatment of mine drainage waters involves pH adjustment, but this often results in excessive sludge formation and removal of nontoxic species such as magnesium and calcium. Theoretical consideration of the stability of metal carbonate species suggests that the target metals could be removed from solution by coprecipitation with calcium carbonate. The U.S. Geological Survey has developed a limestone-based process for remediation of acid mine drainage that increases calcium carbonate saturation. This treatment could then be coupled with carbonate coprecipitation as an innovative method for removal of toxic metals from circumneutral mine drainage waters. The new process was termed the carbonate coprecipitation (CCP) process. The CCP process was tested at the laboratory scale using a synthetic mine water containing 50 mg/L each of Mn and Zn. Best results showed over 95% removal of both Mn and Zn in less than 2 h of contact in a limestone channel. The process was then tested on a sample of water from the Palmerton zinc superfund site, near Palmerton, Pennsylvania, containing over 300 mg/L Zn and 60 mg/L Mn. Treatment of this water resulted in removal of over 95% of the Zn and 40% of the Mn in the limestone channel configuration. Because of the potential economic advantages of the CCP process, further research is recommended for refinement of the process for the Palmerton water and for application to other mining impacted waters as well. ?? Mary Ann Liebert, Inc.

  8. In field arsenic removal from natural water by zero-valent iron assisted by solar radiation

    Cornejo, Lorena; Lienqueo, Hugo; Arenas, Maria; Acarapi, Jorge; Contreras, David; Yanez, Jorge; Mansilla, Hector D.

    2008-01-01

    An in situ arsenic removal method applicable to highly contaminated water is presented. The method is based in the use of steel wool, lemon juice and solar radiation. The method was evaluated using water from the Camarones River, Atacama Desert in northern Chile, in which the arsenic concentration ranges between 1000 and 1300 μg L -1 . Response surface method analysis was used to optimize the amount of zero-valent iron (steel wool) and the citrate concentration (lemon juice) to be used. The optimal conditions when using solar radiation to remove arsenic from natural water from the Camarones river are: 1.3 g L -1 of steel wool and one drop (ca. 0.04 mL) of lemon juice. Under these conditions, removal percentages are higher than 99.5% and the final arsenic concentration is below 10 μg L -1 . This highly effective arsenic removal method is easy to use and inexpensive to implement. - An in situ arsenic removal method applicable to highly contaminated waters by using zero-valent iron, citrate and solar radiation was developed

  9. Comparative study of different types of granular activated carbon in removing medium level radon from water

    Alabdula'aly, A.I.; Maghrawy, H.B.

    2011-01-01

    Granular activated carbon (GAC) has proven its effectiveness in removing radon from water supplies. Laboratory and pilot plant studies were carried out using three different types of activated carbons (F-300, F-400, and HD-4000) to remove radon from water supply. From the experimental kinetic study, the data indicated that at least 6 h are needed to attain equilibrium between radon activity adsorbed onto carbon and its concentration in the aqueous phase. Also, it showed that HD-4000 has higher capacity for removing radon than the other two investigated carbons F-300 and F-400. The adsorption isotherms were satisfactorily explained by Freundlich equation. In the pilot plant study, the performance of the three activated carbons in removing radon at medium concentration (∼111 Bq dm -3 ) was evaluated over 60 days of continuous water flow. Four empty-bed contact times (EBCTs) corresponding to four bed depths were continuously monitored and the corresponding steady state adsorption-decay constant values were calculated and the efficiency of each carbon was used to provide a facet for comparison. The γ-radiation exposure rate distribution throughout each GAC bed was measured and compared. This study, despite paucity of literature in this field, is useful for designing a GAC adsorption system for the removal of medium level radon concentration from water supplies. (author)

  10. Preozonation Effect on Total Organic Carbon Removal in Surface Water Treatment

    Ali Torabian

    2006-06-01

    Full Text Available In drinking water treatment, preozonation is often applied in order to control the microorganisms and taste and odor causing materials, which may influence organics removal by preoxidation and adsorption. Using commercial and natural water humic substances, the positive effect of preozonation as an aid to coagulation-flocculation of these compounds was confirmed by removal of TOC removal in Tehranpars Water Treatment Plant in Tehran. These experiments were conducted as bench-scale studies through a series of jar tests using different pH coagulant dosages and total organic carbon concentration of approximately 4, 8 and 12 mg/L. In addition to TOC removal, the existence of an optimum preozonation dose (OPZD was also confirmed. Experiments show that preozonation can improve coagulation and flocculation depending on influent TOC concentration of raw water. The results demonstrate different effects of preozonation on removal of influent TOC. Preozonation showed a positive effect on a system with low influent TOC and very low molecular weight (noncolloidal humic substances.

  11. In field arsenic removal from natural water by zero-valent iron assisted by solar radiation

    Cornejo, Lorena [Departamento de Quimica, Facultad de Ciencias, Universidad de Tarapaca, Casilla 7-D, Arica (Chile); Laboratorio de Investigaciones Medioambientales de Zonas Aridas, LIMZA, Centro de Investigaciones del Hombre en el Desierto, CIHDE, Arica (Chile)], E-mail: lorenacp@uta.cl; Lienqueo, Hugo; Arenas, Maria [Departamento de Quimica, Facultad de Ciencias, Universidad de Tarapaca, Casilla 7-D, Arica (Chile); Acarapi, Jorge [Departamento de Quimica, Facultad de Ciencias, Universidad de Tarapaca, Casilla 7-D, Arica (Chile); Laboratorio de Investigaciones Medioambientales de Zonas Aridas, LIMZA, Centro de Investigaciones del Hombre en el Desierto, CIHDE, Arica (Chile); Contreras, David; Yanez, Jorge; Mansilla, Hector D. [Facultad de Ciencias Quimicas, Universidad de Concepcion, Casilla 160C, Concepcion (Chile)

    2008-12-15

    An in situ arsenic removal method applicable to highly contaminated water is presented. The method is based in the use of steel wool, lemon juice and solar radiation. The method was evaluated using water from the Camarones River, Atacama Desert in northern Chile, in which the arsenic concentration ranges between 1000 and 1300 {mu}g L{sup -1}. Response surface method analysis was used to optimize the amount of zero-valent iron (steel wool) and the citrate concentration (lemon juice) to be used. The optimal conditions when using solar radiation to remove arsenic from natural water from the Camarones river are: 1.3 g L{sup -1} of steel wool and one drop (ca. 0.04 mL) of lemon juice. Under these conditions, removal percentages are higher than 99.5% and the final arsenic concentration is below 10 {mu}g L{sup -1}. This highly effective arsenic removal method is easy to use and inexpensive to implement. - An in situ arsenic removal method applicable to highly contaminated waters by using zero-valent iron, citrate and solar radiation was developed.

  12. REMOVAL OF CHROMIUM FROM AQUEOUS SOLUTION USING LOCALLY AVAILABLE INEXPENSIVE TARO AND WATER HYACINTH AS BIOSORBENT

    Shahjalal Khandaker

    2016-04-01

    Full Text Available In this investigation, locally available and inexpensive Taro and Water Hyacinth were used as biosorbents to remove chromium from synthetic wastewater. The removal of this metal ion from water in the batch and column method have been studied and discussed. Adsorption kinetics and equilibrium isotherm studies were also carried out. The material exhibits good adsorption capacity and the data follow both Freundlich and Langmuir models. Scanning Electronic Microscopic image was also used to understand the surface characteristics of biosorbent before and after biosorption studies. Effects of various factors such as pH, adsorbent dose, adsorbate initial concentration, particle size etc. were analyzed. The initial concentrations of chromium were considered 5-30mgL-1 in batch method and only 4mgL-1 in column method. The maximum chromium adsorbed was 1.64 mgg-1 and 4.44 mgg-1 in Batch method and 1.15 mgg-1 and 0.75 mgg-1 in Column method. Batch and Column desorption and regeneration studies were conducted. Column desorption studies indicated that both of these biosorbents could be reused for removing heavy metals. Results of the laboratory experiments show that the performance of Taro and Water Hyacinth prove that they can effectively be used as low cost biosorbents for the removal of chromium from wastewater.KEYWORDS:   adsorption; chromium removal; Taro; water hyacinth; batch method; column studies

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

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

    2015-01-01

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

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

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

    2015-10-15

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

  15. Application of nanofiltration for the removal of carbamazepine, diclofenac and ibuprofen from drinking water sources.

    Vergili, I

    2013-09-30

    Pharmaceutical active compounds (PhACs) are persistent during the process used to treat drinking water and, because drinking water treatment plants are not specifically designed to remove PhACs, these compounds are found in drinking water. Although there are currently no regulations or drinking water directives for PhACs, precautionary principles suggest ensuring maximal removal of PhACs through improved or existing treatment techniques. This study was designed to investigate the performance of a nanofiltration membrane in cross-flow filtration equipment for the removal of three PhACs [carbamazepine (CBZ), diclofenac (DIC) and ibuprofen (IBU)] that were spiked in water taken from a drinking water treatment plant using surface water. Because of their low solubilities, high log Kow values, low dipole moments and negative charges, higher rejection values were obtained for DIC and IBU. Low to moderate rejection values were most likely due to the small molecular sizes of the PhACs (i.e., MW water. Flux declines obtained from DIC studies was attributed to the adsorption of DIC ions inside the membrane pores, which decreases the flux. The most evident change in the FT-IR spectrum after nanofiltration was the appearance of new intense bands at 1072 cm(-1) and 1011 cm(-1), indicating the deposition of calcium salts on the membrane surface. Copyright © 2013 Elsevier Ltd. All rights reserved.

  16. Water and oxygen induced degradation of small molecule organic solar cells

    Hermenau, Martin; Riede, Moritz; Leo, Karl

    2011-01-01

    Small molecule organic solar cells were studied with respect to water and oxygen induced degradation by mapping the spatial distribution of reaction products in order to elucidate the degradation patterns and failure mechanisms. The active layers consist of a 30 nm bulk heterojunction formed......,4′-diamine p-doped with C60F36 (MeO-TPD:C60F36), which acted as hole transporting layer. Indium-tin-oxide (ITO) and aluminum served as hole and electron collecting electrode, respectively. Time-of-flight secondary ion mass spectrometry (TOF-SIMS) and X-ray photoelectron spectroscopy (XPS) in conjunction...... of aluminum oxide at the BPhen/Al interface, and diffusion of water into the ZnPc:C60 layer where ZnPc becomes oxidized. Finally, diffusion from the electrodes was found to have no or a negligible effect on the device lifetime....

  17. Nitrogen removal and greenhouse gas emissions from constructed wetlands receiving tile drainage water.

    Groh, Tyler A; Gentry, Lowell E; David, Mark B

    2015-05-01

    Loss of nitrate from agricultural lands to surface waters is an important issue, especially in areas that are extensively tile drained. To reduce these losses, a wide range of in-field and edge-of-field practices have been proposed, including constructed wetlands. We re-evaluated constructed wetlands established in 1994 that were previously studied for their effectiveness in removing nitrate from tile drainage water. Along with this re-evaluation, we measured the production and flux of greenhouse gases (GHGs) (CO, NO, and CH). The tile inlets and outlets of two wetlands were monitored for flow and N during the 2012 and 2013 water years. In addition, seepage rates of water and nitrate under the berm and through the riparian buffer strip were measured. Greenhouse gas emissions from the wetlands were measured using floating chambers (inundated fluxes) or static chambers (terrestrial fluxes). During this 2-yr study, the wetlands removed 56% of the total inlet nitrate load, likely through denitrification in the wetland. Some additional removal of nitrate occurred in seepage water by the riparian buffer strip along each berm (6.1% of the total inlet load, for a total nitrate removal of 62%). The dominant GHG emitted from the wetlands was CO, which represented 75 and 96% of the total GHG emissions during the two water years. The flux of NO contributed between 3.7 and 13% of the total cumulative GHG flux. Emissions of NO were 3.2 and 1.3% of the total nitrate removed from wetlands A and B, respectively. These wetlands continue to remove nitrate at rates similar to those measured after construction, with relatively little GHG gas loss. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

  18. Enteric virus removal from water by coal-based sorbents: development of low-cost water filters

    Chaudhuri, M.; Sattar, S.A.

    1986-01-01

    Using poliovirus type 1 (Sabin) and dechlorinated tap water, several coal-based sorbents were tested for their capacity to remove viruses from water. The sorbents included bituminous coal from Giridih, India, pretreated/impregnated with either alum, ferric hydroxide, lime or manganese dioxide. Filtrasorb-400, commercially available active carbon, was used as a reference. In batch tests, with input virus concentration of 2.34-2.83x10/sup 6/ PFU/1 and sorbent concentration of 10 g/l, alum pretreated coal removed about 96% of the virus when pH of the water was between 6.3 and 8.9. Virus sorption was rapid and a plateau was reached in 30 min. Compared with the active carbon, alum pretreated coal exhibited greater sorption energy and about one log higher limiting poliovirus sorption capacity. Downflow column study indicated the potential of alum pretreated coal as a filter media for removing enteric viruses from water. A previous study showed this sorbent to be capable of removing enteric bacteria as well. Water filters prepared from such low-cost material may prove useful for domestic use in rural areas of India and other developing countries. 19 refs.

  19. Potential for water salvage by removal of non-native woody vegetation from dryland river systems

    Doody, T.M.; Nagler, P.L.; Glenn, E.P.; Moore, G.W.; Morino, K.; Hultine, K.R.; Benyon, R.G.

    2011-01-01

    Globally, expansion of non-native woody vegetation across floodplains has raised concern of increased evapotranspiration (ET) water loss with consequent reduced river flows and groundwater supplies. Water salvage programs, established to meet water supply demands by removing introduced species, show little documented evidence of program effectiveness. We use two case studies in the USA and Australia to illustrate factors that contribute to water salvage feasibility for a given ecological setting. In the USA, saltcedar (Tamarix spp.) has become widespread on western rivers, with water salvage programs attempted over a 50-year period. Some studies document riparian transpiration or ET reduction after saltcedar removal, but detectable increases in river base flow are not conclusively shown. Furthermore, measurements of riparian vegetation ET in natural settings show saltcedar ET overlaps the range measured for native riparian species, thereby constraining the possibility of water salvage by replacing saltcedar with native vegetation. In Australia, introduced willows (Salix spp.) have become widespread in riparian systems in the Murray-Darling Basin. Although large-scale removal projects have been undertaken, no attempts have been made to quantify increases in base flows. Recent studies of ET indicate that willows growing in permanently inundated stream beds have high transpiration rates, indicating water savings could be achieved from removal. In contrast, native Eucalyptus trees and willows growing on stream banks show similar ET rates with no net water salvage from replacing willows with native trees. We conclude that water salvage feasibility is highly dependent on the ecohydrological setting in which the non-native trees occur. We provide an overview of conditions favorable to water salvage. Copyright ?? 2011 John Wiley & Sons, Ltd.

  20. Monitoring the prevalence of nitrosamines in South African waters and their removal using cyclodextrin polyurethanes

    Mhlongo, Sthembile H.; Mamba, Bhekie B.; Krause, Rui W.

    The prevalence of nitrosamines, especially N-nitrosodimethylamine (NDMA), was monitored in three South African water supplies. NDMA a disinfection by-product (DBP) and potent carcinogen, has recently been detected in many drinking water supplies internationally. Besides direct industrial or human-derived contamination, nitrosodimethylamine can be formed through a chemical reaction between monochloroamine and an organic based compound such as dimethylamine which is frequently detected in surface water. It has been suggested that chloramination of surface waters with a high concentration of dissolved organic carbon (DOC) could result in elevated NDMA formation. Growing evidence suggests that NDMA occurs more frequently and at higher concentrations in drinking water systems that practise chloramination compared to systems that use chlorination. In gauging the extent of water contamination by nitrosamines in water distribution systems, especially NDMA, water samples collected from three different water treatment plants that practise chemical drinking water disinfection were qualitatively analysed for the presence of nitrosamines. Solid phase microextraction (SPME) was employed in the extraction of nitrosamines from the water samples and gas chromatography-mass spectrometry (GC-MS), was used in the analysis of the water samples. Trace amounts of NDMA were detected at one of the water treatment plants and in the distribution network. The application of water-insoluble cyclodextrin (CD) polymers in the removal of nitrosamines and potential amine precursors from the water samples was tested. Quantitative removal of NDMA (based on peak area) from the water samples was achieved which suggests that in the water treatment train the use of these nanosponges can be applied in the mitigation of trace contaminants such as NDMA.

  1. Conserved hydrogen bonds and water molecules in MDR HIV-1 protease substrate complexes

    Liu, Zhigang [Wayne State Univ., Detroit, MI (United States); Case Western Reserve Univ., Cleveland, OH (United States); Harbor Hospital Baltimore, MD (United States); Wang, Yong [Wayne State Univ., Detroit, MI (United States); Yedidi, Ravikiran S. [Wayne State Univ., Detroit, MI (United States); National Institutes of Health, Bethesda, MD (United States); Dewdney, Tamaria G. [Wayne State Univ., Detroit, MI (United States); Reiter, Samuel J. [Wayne State Univ., Detroit, MI (United States); Brunzelle, Joseph S. [Northwestern Univ. Feinberg School of Medicine, Chicago, IL (United States); Kovari, Iulia A. [Wayne State Univ., Detroit, MI (United States); Kovari, Ladislau C. [Wayne State Univ., Detroit, MI (United States)

    2012-12-19

    Success of highly active antiretroviral therapy (HAART) in anti-HIV therapy is severely compromised by the rapidly developing drug resistance. HIV-1 protease inhibitors, part of HAART, are losing their potency and efficacy in inhibiting the target. Multi-drug resistant (MDR) 769 HIV-1 protease (resistant mutations at residues 10, 36, 46, 54, 62, 63, 71, 82, 84, 90) was selected for the present study to understand the binding to its natural substrates. The nine crystal structures of MDR769 HIV-1 protease substrate hepta-peptide complexes were analyzed in order to reveal the conserved structural elements for the purpose of drug design against MDR HIV-1 protease. Our structural studies demonstrated that highly conserved hydrogen bonds between the protease and substrate peptides, together with the conserved crystallographic water molecules, played a crucial role in the substrate recognition, substrate stabilization and protease stabilization. Additionally, the absence of the key flap-ligand bridging water molecule might imply a different catalytic mechanism of MDR769 HIV-1 protease compared to that of wild type (WT) HIV-1 protease.

  2. Tuning dissociation using isoelectronically doped graphene and hexagonal boron nitride: Water and other small molecules

    Al-Hamdani, Yasmine S. [Thomas Young Centre and London Centre for Nanotechnology, 17–19 Gordon Street, London WC1H 0AH (United Kingdom); Department of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ (United Kingdom); Alfè, Dario [Thomas Young Centre and London Centre for Nanotechnology, 17–19 Gordon Street, London WC1H 0AH (United Kingdom); Department of Earth Sciences, University College London, Gower Street, London WC1E 6BT (United Kingdom); Lilienfeld, O. Anatole von [Institute of Physical Chemistry and National Center for Computational Design and Discovery of Novel Materials (MARVEL), Department of Chemistry, University of Basel, Klingelbergstrasse 80, CH-4056 Basel (Switzerland); Michaelides, Angelos, E-mail: angelos.michaelides@ucl.ac.uk [Thomas Young Centre and London Centre for Nanotechnology, 17–19 Gordon Street, London WC1H 0AH (United Kingdom); Department of Physics and Astronomy, University College London, Gower Street, London WC1E 6BT (United Kingdom)

    2016-04-21

    Novel uses for 2-dimensional materials like graphene and hexagonal boron nitride (h-BN) are being frequently discovered especially for membrane and catalysis applications. Still however, a great deal remains to be understood about the interaction of environmentally and industrially relevant molecules such as water with these materials. Taking inspiration from advances in hybridising graphene and h-BN, we explore using density functional theory, the dissociation of water, hydrogen, methane, and methanol on graphene, h-BN, and their isoelectronic doped counterparts: BN doped graphene and C doped h-BN. We find that doped surfaces are considerably more reactive than their pristine counterparts and by comparing the reactivity of several small molecules, we develop a general framework for dissociative adsorption. From this a particularly attractive consequence of isoelectronic doping emerges: substrates can be doped to enhance their reactivity specifically towards either polar or non-polar adsorbates. As such, these substrates are potentially viable candidates for selective catalysts and membranes, with the implication that a range of tuneable materials can be designed.

  3. Method of removing tritium in exhaust water in a nuclear equipment

    Iwamoto, T

    1976-05-12

    A method is claimed to increase the efficiency of removing tritium from waste water through adsorption treatment. Steam is produced by heating waste water containing tritium, and it is passed through a tube filled with an adsorbent such as activated alumina, silica gel or zeolite. When a control limiting value is reached by the concentration of tritium within the steam, the flow of steam is stopped, and the adsorption tube is removed from the path of steam flow. Thereafter, another adsorption tube containing the afore-said adsorbent is provided in the steam flow path, and the steam is then allowed to flow again.

  4. Conditioned of process of water removal product radioactive and non-radioactive genesis

    Shevchenko, O.L.

    2011-01-01

    The analysis mode of soluble organic matter in natural humic water drainage channels left bank of Pripyat and its dependence on the hydrodynamic and hydrological factors. Proved the existence of the concentration of 90 Sr in the water on the content of fulvic acid in it. Quantified removal of humic acids of groundwater and surface runoff. Emphasizes the primary role in the removal of humic substances and significant - in the mobilization of 90 Sr processes of secondary swamping of the surface watershed and eutrophication of waterways, which have acquired extensive development on the alienation of the territory for 25 years after the Chernobyl disaster.

  5. Exploratory study on pervaporation membranes for removal of water from water-crude oil emulsions: Final report

    1989-01-01

    Study to explore the feasibility of removing water from oil/water (O/W) and water/oil (W/O) emulsions by means of pervaporation. Initial study involved preparation of simulated O/W and W/O emulsions prepared by mixing water and kerosene of various concentrations and stabilized by adding sodium lauryl sulfate. Preliminary experiments were conducted on 12 membranes fabricated from 2 different materials. One membrane of each type of material was chosen for further work based on the results of the preliminary tests. All experiments were carried out under 2 different downstream pressures and various temperatures.

  6. Identification of Carboxylate, Phosphate, and Phenoxide Functionalities in Deprotonated Molecules Related to Drug Metabolites via Ion-Molecule Reactions with water and Diethylhydroxyborane

    Zhu, Hanyu; Ma, Xin; Kong, John Y.; Zhang, Minli; Kenttämaa, Hilkka I.

    2017-10-01

    Tandem mass spectrometry based on ion-molecule reactions has emerged as a powerful tool for structural elucidation of ionized analytes. However, most currently used reagents were designed to react with protonated analytes, making them suboptimal for acidic analytes that are preferentially detected in negative ion mode. In this work we demonstrate that the phenoxide, carboxylate, and phosphate functionalities can be identified in deprotonated molecules by use of a combination of two reagents, diethylmethoxyborane (DEMB) and water. A novel reagent introduction setup that allowed DEMB and water to be separately introduced into the ion trap region of the mass spectrometer was developed to facilitate fundamental studies of this reaction. A new reagent, diethylhydroxyborane (DEHB), was generated inside the ion trap by hydrolysis of DEMB on introduction of water. Most carboxylates and phenoxides formed a DEHB adduct, followed by addition of one water molecule and subsequent ethane elimination (DEHB adduct +H2O - CH3CH3) as the major product ion. Phenoxides with a hydroxy group adjacent to the deprotonation site and phosphates formed a DEHB adduct, followed by ethane elimination (DEHB adduct - CH3CH3). Deprotonated molecules with strong intramolecular hydrogen bonds or without the aforementioned functionalities, including sulfates, were unreactive toward DEHB/H2O. Reaction mechanisms were explored via isotope labeling experiments and quantum chemical calculations. The mass spectrometry method allowed the differentiation of phenoxide-, carboxylate-, phosphate-, and sulfate-containing analytes. Finally, it was successfully coupled with high-performance liquid chromatography for the analysis of a mixture containing hymecromone, a biliary spasm drug, and its three possible metabolites. [Figure not available: see fulltext.

  7. Removal of Fe(II) from tap water by electrocoagulation technique

    Ghosh, D.; Solanki, H. [Department of Chemical Engineering, Indian Institute of Technology, Guwahati 781039 (India); Purkait, M.K. [Department of Chemical Engineering, Indian Institute of Technology, Guwahati 781039 (India)], E-mail: mihir@iitg.ernet.in

    2008-06-30

    Electrocoagulation (EC) is a promising electrochemical technique for water treatment. In this work electrocoagulation (with aluminum as electrodes) was studied for iron Fe(II) removal from aqueous medium. Different concentration of Fe(II) solution in tap water was considered for the experiment. During EC process, various amorphous aluminum hydroxides complexes with high sorption capacity were formed. The removal of Fe(II) was consisted of two principal steps; (a) oxidation of Fe(II) to Fe(III) and (b) subsequent removal of Fe(III) by the freshly formed aluminum hydroxides complexes by adsorption/surface complexation followed by precipitation. Experiments were carried out with different current densities ranging from 0.01 to 0.04 A/m{sup 2}. It was observed that the removal of Fe(II) increases with current densities. Inter electrode distance was varied from 0.005 to 0.02 m and was found that least inter electrode distance is suitable in order to achieve higher Fe(II) removal. Other parameters such as conductivity, pH and salt concentration were kept constant as per tap water quality. Satisfactory iron removal of around 99.2% was obtained at the end of 35 min of operation from the initial concentration of 25 mg/L Fe(II). Iron concentration in the solution was determined using Atomic absorption spectrophotometer. By products obtained from the electrocoagulation bath were analyzed by SEM image and corresponding elemental analysis (EDAX). Cost estimation for the electrocoagulation was adopted and explained well. Up to 15 mg/L of initial Fe(II) concentration, the optimum total cost was 6.05 US$/m{sup 3}. The EC process for removing Fe(II) from tap water is expected to be adaptable for household use.

  8. Removal of Fe(II) from tap water by electrocoagulation technique

    Ghosh, D.; Solanki, H.; Purkait, M.K.

    2008-01-01

    Electrocoagulation (EC) is a promising electrochemical technique for water treatment. In this work electrocoagulation (with aluminum as electrodes) was studied for iron Fe(II) removal from aqueous medium. Different concentration of Fe(II) solution in tap water was considered for the experiment. During EC process, various amorphous aluminum hydroxides complexes with high sorption capacity were formed. The removal of Fe(II) was consisted of two principal steps; (a) oxidation of Fe(II) to Fe(III) and (b) subsequent removal of Fe(III) by the freshly formed aluminum hydroxides complexes by adsorption/surface complexation followed by precipitation. Experiments were carried out with different current densities ranging from 0.01 to 0.04 A/m 2 . It was observed that the removal of Fe(II) increases with current densities. Inter electrode distance was varied from 0.005 to 0.02 m and was found that least inter electrode distance is suitable in order to achieve higher Fe(II) removal. Other parameters such as conductivity, pH and salt concentration were kept constant as per tap water quality. Satisfactory iron removal of around 99.2% was obtained at the end of 35 min of operation from the initial concentration of 25 mg/L Fe(II). Iron concentration in the solution was determined using Atomic absorption spectrophotometer. By products obtained from the electrocoagulation bath were analyzed by SEM image and corresponding elemental analysis (EDAX). Cost estimation for the electrocoagulation was adopted and explained well. Up to 15 mg/L of initial Fe(II) concentration, the optimum total cost was 6.05 US$/m 3 . The EC process for removing Fe(II) from tap water is expected to be adaptable for household use

  9. Evaluating of arsenic(V) removal from water by weak-base anion exchange adsorbents.

    Awual, M Rabiul; Hossain, M Amran; Shenashen, M A; Yaita, Tsuyoshi; Suzuki, Shinichi; Jyo, Akinori

    2013-01-01

    Arsenic contamination of groundwater has been called the largest mass poisoning calamity in human history and creates severe health problems. The effective adsorbents are imperative in response to the widespread removal of toxic arsenic exposure through drinking water. Evaluation of arsenic(V) removal from water by weak-base anion exchange adsorbents was studied in this paper, aiming at the determination of the effects of pH, competing anions, and feed flow rates to improvement on remediation. Two types of weak-base adsorbents were used to evaluate arsenic(V) removal efficiency both in batch and column approaches. Anion selectivity was determined by both adsorbents in batch method as equilibrium As(V) adsorption capacities. Column studies were performed in fixed-bed experiments using both adsorbent packed columns, and kinetic performance was dependent on the feed flow rate and competing anions. The weak-base adsorbents clarified that these are selective to arsenic(V) over competition of chloride, nitrate, and sulfate anions. The solution pH played an important role in arsenic(V) removal, and a higher pH can cause lower adsorption capacities. A low concentration level of arsenic(V) was also removed by these adsorbents even at a high flow rate of 250-350 h(-1). Adsorbed arsenic(V) was quantitatively eluted with 1 M HCl acid and regenerated into hydrochloride form simultaneously for the next adsorption operation after rinsing with water. The weak-base anion exchange adsorbents are to be an effective means to remove arsenic(V) from drinking water. The fast adsorption rate and the excellent adsorption capacity in the neutral pH range will render this removal technique attractive in practical use in chemical industry.

  10. Control of unidirectional transport of single-file water molecules through carbon nanotubes in an electric field.

    Su, Jiaye; Guo, Hongxia

    2011-01-25

    The transport of water molecules through nanopores is not only crucial to biological activities but also useful for designing novel nanofluidic devices. Despite considerable effort and progress that has been made, a controllable and unidirectional water flow is still difficult to achieve and the underlying mechanism is far from being understood. In this paper, using molecular dynamics simulations, we systematically investigate the effects of an external electric field on the transport of single-file water molecules through a carbon nanotube (CNT). We find that the orientation of water molecules inside the CNT can be well-tuned by the electric field and is strongly coupled to the water flux. This orientation-induced water flux is energetically due to the asymmetrical water-water interaction along the CNT axis. The wavelike water density profiles are disturbed under strong field strengths. The frequency of flipping for the water dipoles will decrease as the field strength is increased, and the flipping events vanish completely for the relatively large field strengths. Most importantly, a critical field strength E(c) related to the water flux is found. The water flux is increased as E is increased for E ≤ E(c), while it is almost unchanged for E > E(c). Thus, the electric field offers a level of governing for unidirectional water flow, which may have some biological applications and provides a route for designing efficient nanopumps.

  11. Rapid removal of fine particles from mine water using sequential processes of coagulation and flocculation

    Jang, M.; Lee, H.J.; Shim, Y. [Korean Mine Reclamation Corporation MIRECO, Seoul (Republic of Korea)

    2010-07-01

    The processes of coagulation and flocculation using high molecular weight long-chain polymers were applied to treat mine water having fine flocs of which about 93% of the total mass was less than 3.02 {mu} m, representing the size distribution of fine particles. Six different combinations of acryl-type anionic flocculants and polyamine-type cationic coagulants were selected to conduct kinetic tests on turbidity removal in mine water. Optimization studies on the types and concentrations of the coagulant and flocculant showed that the highest rate of turbidity removal was obtained with 10 mg L{sup -1} FL-2949 (coagulant) and 12 mg L{sup -1} A333E (flocculant), which was about 14.4 and 866.7 times higher than that obtained with A333E alone and that obtained through natural precipitation by gravity, respectively. With this optimized condition, the turbidity of mine water was reduced to 0 NTU within 20 min. Zeta potential measurements were conducted to elucidate the removal mechanism of the fine particles, and they revealed that there was a strong linear relationship between the removal rate of each pair of coagulant and flocculant application and the zeta potential differences that were obtained by subtracting the zeta potential of flocculant-treated mine water from the zeta potential of coagulant-treated mine water. Accordingly, through an optimization process, coagulation-flocculation by use of polymers could be advantageous to mine water treatment, because the process rapidly removes fine particles in mine water and only requires a small-scale plant for set-up purposes owing to the short retention time in the process.

  12. Pharmaceuticals as emerging contaminants and their removal from water. A review.

    Rivera-Utrilla, José; Sánchez-Polo, Manuel; Ferro-García, María Ángeles; Prados-Joya, Gonzalo; Ocampo-Pérez, Raúl

    2013-10-01

    The main objective of this study was to conduct an exhaustive review of the literature on the presence of pharmaceutical-derived compounds in water and on their removal. The most representative pharmaceutical families found in water were described and related water pollution issues were analyzed. The performances of different water treatment systems in the removal of pharmaceuticals were also summarized. The water treatment technologies were those based on conventional systems (chlorine, chlorine dioxide, wastewater treatment plants), adsorption/bioadsorption on activated carbon (from lotus stalks, olive-waste cake, coal, wood, plastic waste, cork powder waste, peach stones, coconut shell, rice husk), and advanced oxidation processes by means of ozonation (O₃, O₃/H₂O₂, O₃/activated carbon, O₃/biological treatment), photooxidation (UV, UV/H₂O₂, UV/K₂S₂O₈, UV/TiO₂, UV/H₂O₂/TiO₂, UV/TiO₂/activated carbon, photo-Fenton), radiolysis (e-Beam, ⁶⁰Co, ¹³⁷Cs. Additives used: H₂O₂, SO₃²⁻, HCO₃⁻, CH₃₋OH, CO₃²⁻, or NO₃⁻), and electrochemical processes (Electrooxidation without and with active chlorine generation). The effect of these treatments on pharmaceutical compounds and the advantages and disadvantages of different methodologies used were described. The most important parameters of the above water treatment systems (experimental conditions, removal yield, pharmaceutical compound mineralization, TOC removal, toxicity evolution) were indicated. The key publications on pharmaceutical removal from water were summarized. Copyright © 2013 Elsevier Ltd. All rights reserved.

  13. Rapid removal of fine particles from mine water using sequential processes of coagulation and flocculation.

    Jang, Min; Lee, Hyun-Ju; Shim, Yonsik

    2010-04-01

    The processes of coagulation and flocculation using high molecular weight long-chain polymers were applied to treat mine water having fine flocs of which about 93% of the total mass was less than 3.02 microm, representing the size distribution of fine particles. Six different combinations of acryl-type anionic flocculants and polyamine-type cationic coagulants were selected to conduct kinetic tests on turbidity removal in mine water. Optimization studies on the types and concentrations of the coagulant and flocculant showed that the highest rate of turbidity removal was obtained with 10 mg L(-1) FL-2949 (coagulant) and 12 mg L(-1) A333E (flocculant), which was about 14.4 and 866.7 times higher than that obtained with A333E alone and that obtained through natural precipitation by gravity, respectively. With this optimized condition, the turbidity of mine water was reduced to 0 NTU within 20 min. Zeta potential measurements were conducted to elucidate the removal mechanism of the fine particles, and they revealed that there was a strong linear relationship between the removal rate of each pair of coagulant and flocculant application and the zeta potential differences that were obtained by subtracting the zeta potential of flocculant-treated mine water from the zeta potential of coagulant-treated mine water. Accordingly, through an optimization process, coagulation-flocculation by use of polymers could be advantageous to mine water treatment, because the process rapidly removes fine particles in mine water and only requires a small-scale plant for set-up purposes owing to the short retention time in the process.

  14. Removal of lead and fluoride from contaminated water using exhausted coffee grounds based bio-sorbent.

    Naga Babu, A; Reddy, D Srinivasa; Kumar, G Suresh; Ravindhranath, K; Krishna Mohan, G V

    2018-07-15

    Water pollution by industrial and anthropogenic actives has become a serious threat to the environment. World Health Organization (WHO) has identified that lead and fluoride amid the environmental pollutants are most poisonous water contaminants with devastating impact on the human race. The present work proposes a study on economical bio-adsorbent based technique using exhausted coffee grounds in the removal of lead and fluoride contaminants from water. The exhausted coffee grounds gathered from industrial wastes have been acid-activated and examined for their adsorption capacity. The surface morphology and elemental characterization of pre-and-post adsorption operations by FESEM, EDX and FTIR spectral analysis confirmed the potential of the exhausted coffee ground as successful bio-sorbent. However, thermodynamic analysis confirmed the adsorption to be spontaneous physisorption with Langmuir mode of homogenous monolayer deposition. The kinetics of adsorption is well defined by pseudo second order model for both lead and fluoride. A significant quantity of lead and fluoride is removed from the synthetic contaminated water by the proposed bio-sorbent with the respective sorption capabilities of 61.6 mg/g and 9.05 mg/g. However, the developed bio-sorbent is also recyclable and is capable of removing the lead and fluoride from the domestic and industrial waste-water sources with an overall removal efficiency of about 90%. Copyright © 2018 Elsevier Ltd. All rights reserved.

  15. Application of cellulose nanofibers to remove water-based flexographic inks from wastewaters.

    Balea, Ana; Monte, M Concepción; de la Fuente, Elena; Negro, Carlos; Blanco, Ángeles

    2017-02-01

    Water-based or flexographic inks in paper and plastic industries are more environmentally favourable than organic solvent-based inks. However, their use also creates new challenges because they remain dissolved in water and alter the recycling process. Conventional deinking technologies such as flotation processes do not effectively remove them. Adsorption, coagulation/flocculation, biological and membrane processes are either expensive or have negative health impacts, making the development of alternative methods necessary. Cellulose nanofibers (CNF) are biodegradable, and their structural and mechanical properties are useful for wastewater treatment. TEMPO-oxidised CNF have been evaluated for the decolourisation of wastewaters that contained copper phthalocyanine blue, carbon black and diarlyide yellow pigments. CNF in combination with a cationic polyacrylamide (cPAM) has also been tested. Jar-test methodology was used to evaluate the efficiency of the different treatments and cationic/anionic demand, turbidity and ink concentration in waters were measured. Results show that dual-component system for ink removal has a high potential as an alternative bio-based adsorbent for the removal of water-based inks. In addition, experiments varying CNF and cPAM concentrations were performed to optimise the ink-removal process. Ink concentration reductions of 100%, 87.5% and 83.3% were achieved for copper phthalocyanine blue, carbon black and diarlyide yellow pigments, respectively. Flocculation studies carried out show the decolourisation mechanism during the dual-component treatment of wastewaters containing water-based inks.

  16. [Interactions of DNA bases with individual water molecules. Molecular mechanics and quantum mechanics computation results vs. experimental data].

    Gonzalez, E; Lino, J; Deriabina, A; Herrera, J N F; Poltev, V I

    2013-01-01

    To elucidate details of the DNA-water interactions we performed the calculations and systemaitic search for minima of interaction energy of the systems consisting of one of DNA bases and one or two water molecules. The results of calculations using two force fields of molecular mechanics (MM) and correlated ab initio method MP2/6-31G(d, p) of quantum mechanics (QM) have been compared with one another and with experimental data. The calculations demonstrated a qualitative agreement between geometry characteristics of the most of local energy minima obtained via different methods. The deepest minima revealed by MM and QM methods correspond to water molecule position between two neighbor hydrophilic centers of the base and to the formation by water molecule of hydrogen bonds with them. Nevertheless, the relative depth of some minima and peculiarities of mutual water-base positions in' these minima depend on the method used. The analysis revealed insignificance of some differences in the results of calculations performed via different methods and the importance of other ones for the description of DNA hydration. The calculations via MM methods enable us to reproduce quantitatively all the experimental data on the enthalpies of complex formation of single water molecule with the set of mono-, di-, and trimethylated bases, as well as on water molecule locations near base hydrophilic atoms in the crystals of DNA duplex fragments, while some of these data cannot be rationalized by QM calculations.

  17. A review of cyanobacteria and cyanotoxins removal/inactivation in drinking water treatment.

    Westrick, Judy A; Szlag, David C; Southwell, Benjamin J; Sinclair, James

    2010-07-01

    This review focuses on the efficiency of different water treatment processes for the removal of cyanotoxins from potable water. Although several investigators have studied full-scale drinking water processes to determine the efficiency of cyanotoxin inactivation, many of the studies were based on ancillary practice. In this context, "ancillary practice" refers to the removal or inactivation of cyanotoxins by standard daily operational procedures and without a contingency operational plan utilizing specific treatment barriers. In this review, "auxiliary practice" refers to the implementation of inactivation/removal treatment barriers or operational changes explicitly designed to minimize risk from toxin-forming algae and their toxins to make potable water. Furthermore, the best drinking water treatment practices are based on extension of the multibarrier approach to remove cyanotoxins from water. Cyanotoxins are considered natural contaminants that occur worldwide and specific classes of cyanotoxins have shown regional prevalence. For example, freshwaters in the Americas often show high concentrations of microcystin, anatoxin-a, and cylindrospermopsin, whereas Australian water sources often show high concentrations of microcystin, cylindrospermopsin, and saxitoxins. Other less frequently reported cyanotoxins include lyngbyatoxin A, debromoaplysiatoxin, and beta-N-methylamino-L-alanine. This review focuses on the commonly used unit processes and treatment trains to reduce the toxicity of four classes of cyanotoxins: the microcystins, cylindrospermopsin, anatoxin-a, and saxitoxins. The goal of this review is to inform the reader of how each unit process participates in a treatment train and how an auxiliary multibarrier approach to water treatment can provide safer water for the consumer.

  18. Nuclear reactor with makeup water assist from residual heat removal system

    Schulz, T.L.; Corletti, M.M.

    1994-01-01

    A pressurized water nuclear reactor uses its residual heat removal system to make up water in the reactor coolant circuit by pumping water from an in-containment refueling water storage tank during staged depressurization of the coolant circuit, the final stage including passive emergency cooling by gravity feed from the refueling water storage tank to the coolant circuit and to flood the containment building. When depressurization commences due to inadvertence or a manageable leak, the residual heat removal system is activated manually and avoids the final stage of depressurization with its flooding of the containment when such action is not necessary, but does not prevent the final stage when it is necessary. A high pressure makeup water storage tank coupled to the reactor coolant circuit holds makeup coolant at the operational pressure of the reactor. The staged depressurization system vents the coolant circuit to the containment, thus reducing the supply of makeup coolant. The level of makeup coolant can be sensed to trigger opening of successive depressurization conduits. The residual heat removal system can also be coupled in a loop with the refueling water supply tanks for cooling the tank. (Author)

  19. Effect of Co-Contaminant on Denitrification Removal of Nitrate in Drinking Water

    Arzu KILIÇ

    2012-12-01

    Full Text Available In recent years, nitrogenous fertilizers used in agriculture, unconscious and without treatment wastewater is discharged led to an increase in groundwater nitrate pollution. In many countries, nitrate concentration in the ground waters used as drinking water source exceeded the maximum allowable concentration of 10 mg/L NO3-N. According to a study, some wells in the Harran Plain contain nitrate as high as 180 mg/L NO3--N and the average concentration for whole plain is 35 mg/L NO3--N (Yesilnacar et al., 2008. Additionally, increased water consumption, unconscious use of fertilizers and pesticides has led to the emergence of co-contaminant in drinking water. Recently, hazardous to human health co-contaminant such as arsenic, pesticides, perchlorate, selenate, chromate, uranium are observed in the nitrate pollution drinking water. There are many processes used for the removal of nitrate. The physical–chemical technologies that can be used for nitrate removal are reverse osmosis, ion exchange and electrodialysis (Alvarez et al., 2007. Important disadvantages of these processes are their poor selectivity, high operation and maintenance costs and the generation of brine wastes after treatment. Consequently, biological treatment processes to convert nitrates to benign dinitrogen gas, could be an interesting alternative for the remediation of groundwater contaminated with nitrates. The aim of this article, effective and cheap method for the removal of nitrate from drinking water biological denitrification is to examine the usability of contaminated drinking water with co-contaminant pollutions.

  20. PVP capped silver nanocubes assisted removal of glyphosate from water-A photoluminescence study.

    Sarkar, Sumit; Das, Ratan

    2017-10-05

    Glyphosate [N-phosphono-methylglycine (PMG)] is the most used herbicide worldwide and it has been reported very recently that Glyphosate is very harmful and can produce lots of diseases such as alzheimer and parkinson's disease, depression, cancer, infertility including genotoxic effects. As it is mostly present in stable water body and ground water system, its detection and removal is very important. Here, we have shown a fluorescence technique for the removal of glyphosate from water using chemically synthesized polyvinylpyrrolidone (PVP) silver nanocrystals. Transmission Electron Microscopy (TEM) study shows the average size of silver nanocrystals of 100nm approximately with a morphology of cubic shape. Glyphosate does not show absorption in the visible region. But both glyphosate and silver nanocrystals show strong fluorescence in the visible region. So, photoluminescence study has been successfully utilized to detect the glyphosate in water samples and on treating the glyphosate contaminated water sample with silver nanocrystals, the sample shows no emission peak of glyphosate at 458nm. Thus, this approach is a promising and very rapid method for the detection and removal of glyphosate from water samples on treatment with silver nanocubes. NMR spectra further confirms that the silver nanocrystals treated contaminated water samples are glyphosate free. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Removal of tetracycline from contaminated water by Moringa oleifera seed preparations.

    Santos, Andréa F S; Matos, Maria; Sousa, Ângela; Costa, Cátia; Nogueira, Regina; Teixeira, José A; Paiva, Patrícia M G; Parpot, Pier; Coelho, Luana C B B; Brito, António G

    2016-01-01

    The aim of this study was to evaluate tetracycline antibiotic (TA) removal from contaminated water by Moringa oleifera seed preparations. The composition of synthetic water approximate river natural contaminated water and TA simulated its presence as an emerging pollutant. Interactions between TA and protein preparations (extract; fraction and lectin) were also evaluated. TA was determined by solid-phase extraction followed by high-performance liquid chromatography-mass spectrometry. Moringa extract and flour removed TA from water. The extract removed TA in all concentrations, and better removal (40%) was obtained with 40 mg L(-1); seed flour (particles  5 mm (0.50 g L(-1)) removed 55% of antibiotic. Interactions between TA and seed preparations were assayed by haemagglutinating activity (HA). Specific HA (SHA) of extract (pH 7) was abolished with tetracycline (5 mg L(-1)); fraction (75%) and lectin HA (97%) were inhibited with TA. Extract SHA decreased by 75% at pH 8. Zeta potential (ZP) of extract 700 mg L(-1) and tetracycline 50 mg L(-1) , pH range 5-8, showed different results. Extract ZP was more negative (-10.73 to -16.00 mV) than tetracycline ZP (-0.27 to -20.15 mV); ZP difference was greater in pH 8. The focus of this study was achieved since Moringa preparations removed TA from water and compounds interacting with tetracycline involved at least lectin-binding sites. This is a natural process, which do not promote environmental damage.

  2. Removal of natural organic matter in drinking water treatment by coagulation: A comprehensive review.

    Sillanpää, Mika; Ncibi, Mohamed Chaker; Matilainen, Anu; Vepsäläinen, Mikko

    2018-01-01

    Natural organic matter (NOM) is a complex matrix of organic substances produced in (or channeled to) aquatic ecosystems via various biological, geological and hydrological cycles. Such variability is posing a serious challenge to most water treatment technologies, especially the ones designed to treat drinking water supplies. Lately, in addition to the fluctuating composition of NOM, a substantial increase of its concentration in fresh waters, and also municipal wastewater effluents, has been reported worldwide, which justifies the urgent need to develop highly efficient and versatile water treatment processes. Coagulation is among the most applied processes for water and wastewater treatment. The application of coagulation to remove NOM from drinking water supplies has received a great deal of attention from researchers around the world because it was efficient and helped avoiding the formation of disinfection by products (DBPs). Nonetheless, with the increased fluctuation of NOM in water (concentration and composition), the efficiency of conventional coagulation was substantially reduced, hence the need to develop enhanced coagulation processes by optimizing the operating conditions (mainly the amount coagulants and pH), developing more efficient inorganic or organic coagulants, as well as coupling coagulation with other water treatment technologies. In the present review, recent research studies dealing with the application of coagulation for NOM removal from drinking water supplies are presented and compared. In addition, integration schemes combining coagulation and other water treatment processes are presented, including membrane filtration, oxidation, adsorption and others processes. Copyright © 2017 Elsevier Ltd. All rights reserved.

  3. Chitosan Coagulation to Improve Microbial and Turbidity Removal by Ceramic Water Filtration for Household Drinking Water Treatment

    Abebe, Lydia S.; Chen, Xinyu; Sobsey, Mark D.

    2016-01-01

    The use of porous ceramic filters is promoted globally for household water treatment, but these filters are ineffective in removing viruses from water. In order to increase virus removal, we combine a promising natural coagulant, chitosan, as a pretreatment for ceramic water filters (CWFs) and evaluate the performance of this dual barrier water treatment system. Chitosan is a non-toxic and biodegradable organic polymer derived by simple chemical treatments from chitin, a major source of which is the leftover shells of crustacean seafoods, such as shrimp, prawns, crabs, and lobsters. To determine the effectiveness of chitosan, model test water was contaminated with Escherichia coli K011 and coliphage MS2 as a model enteric bacterium and virus, respectively. Kaolinite clay was used to model turbidity. Coagulation effectiveness of three types of modified chitosans was determine at various doses ranging from 5 to 30 mg/L, followed by flocculation and sedimentation. The pre-treated supernatant water was then decanted into the CWF for further treatment by filtration. There were appreciable microbial removals by chitosan HCl, acetate, and lactate pretreatment followed by CWF treatment, with mean reductions (95% CI) between 4.7 (±1.56) and 7.5 (±0.02) log10 for Escherichia coli, and between 2.8 (±0.10) and 4.5 (±1.04) log10 for MS2. Turbidity reduction with chitosan treatment and filtration consistently resulted in turbidities turbidity standards of the US EPA and guidance by the World Health Organization (WHO). According to WHO health-based microbial removal targets for household water treatment technology, chitosan coagulation achieved health protective targets for both viruses and bacteria. Therefore, the results of this study support the use of chitosan to improve household drinking water filtration processes by increasing virus and bacteria reductions. PMID:26927152

  4. Chitosan Coagulation to Improve Microbial and Turbidity Removal by Ceramic Water Filtration for Household Drinking Water Treatment

    Lydia S. Abebe

    2016-02-01

    Full Text Available The use of porous ceramic filters is promoted globally for household water treatment, but these filters are ineffective in removing viruses from water. In order to increase virus removal, we combine a promising natural coagulant, chitosan, as a pretreatment for ceramic water filters (CWFs and evaluate the performance of this dual barrier water treatment system. Chitosan is a non-toxic and biodegradable organic polymer derived by simple chemical treatments from chitin, a major source of which is the leftover shells of crustacean seafoods, such as shrimp, prawns, crabs, and lobsters. To determine the effectiveness of chitosan, model test water was contaminated with Escherichia coli K011 and coliphage MS2 as a model enteric bacterium and virus, respectively. Kaolinite clay was used to model turbidity. Coagulation effectiveness of three types of modified chitosans was determine at various doses ranging from 5 to 30 mg/L, followed by flocculation and sedimentation. The pre-treated supernatant water was then decanted into the CWF for further treatment by filtration. There were appreciable microbial removals by chitosan HCl, acetate, and lactate pretreatment followed by CWF treatment, with mean reductions (95% CI between 4.7 (±1.56 and 7.5 (±0.02 log10 for Escherichia coli, and between 2.8 (±0.10 and 4.5 (±1.04 log10 for MS2. Turbidity reduction with chitosan treatment and filtration consistently resulted in turbidities < 1 NTU, which meet turbidity standards of the US EPA and guidance by the World Health Organization (WHO. According to WHO health-based microbial removal targets for household water treatment technology, chitosan coagulation achieved health protective targets for both viruses and bacteria. Therefore, the results of this study support the use of chitosan to improve household drinking water filtration processes by increasing virus and bacteria reductions.

  5. The use of capacitive deionization with carbon aerogel electrodes to remove inorganic contaminants from water

    Farmer, J.C.; Fix, D.V.; Mack, G.V.; Pekala, R.W.; Poco, J.F.

    1995-01-01

    The capacitive deionization of water with a stack of carbon aerogel electrodes has been successfully demonstrated for the first time. Unlike ion exchange, one of the more conventional deionization processes, no chemicals were required for regeneration of the system. Electricity was used instead. Water with various anions and cations was pumped through the electrochemical cell. After polarization, ions were electrostatically removed from the water and held in the electric double layers formed at electrode surfaces. The water leaving the cell was purified, as desired

  6. Phosphonate removal from discharged circulating cooling water using iron-carbon micro-electrolysis.

    Zhou, Zhen; Qiao, Weimin; Lin, Yangbo; Shen, Xuelian; Hu, Dalong; Zhang, Jianqiao; Jiang, Lu-Man; Wang, Luochun

    2014-01-01

    Phosphonate is a commonly used corrosion and scale inhibitor for a circulating cooling water (CCW) system. Its discharge could cause eutrophication of receiving waters. The iron-carbon (Fe/C) micro-electrolysis technology was used to degrade and remove phosphonate from discharged CCW. The influences of initial pH, Fe/C ratio (FCR) and temperature on phosphonate removal were investigated in a series of batch tests and optimized by response surface methodology. The quadratic model of phosphonate removal was obtained with satisfactory degrees of fitness. The optimum conditions with total phosphorus removal efficiency of 95% were obtained at pH 7.0, FCR of 1.25, and temperature of 45 °C. The phosphonate removal mechanisms were also studied. Phosphonate removal occurred predominantly via two consecutive reactive phases: the degradation of phosphonate complexes (Ca-phosphonate) and the precipitation of Fe/C micro-electrolysis products (PO₄(3-), Ca²⁺ and Fe³⁺).

  7. Recycling of drinking water treatment residue as an additional medium in columns for effective P removal from eutrophic surface water.

    Wang, Changhui; Wu, Yu; Bai, Leilei; Zhao, Yaqian; Yan, Zaisheng; Jiang, Helong; Liu, Xin

    2018-07-01

    This study assesses the feasibility of recycling drinking water treatment residue (DWTR) to treat eutrophic surface water in a one-year continuous flow column test. Heat-treated DWTR was used as an additional medium (2%-4%) in columns in case excessive organic matter and N were released from the DWTR to surface water. The results indicated that with minimal undesirable effects on other water properties, DWTR addition substantially enhanced P removal, rendering P concentrations in treated water oligotrophic and treated water unsuitable for Microcystis aeruginosa breeding. Long-term stable P removal by DWTR-column treatment was mainly attributed to the relatively low P levels in raw water (cycles and multiple pollution control (e.g., Dechloromonas, Geobacter, Leucobacter, Nitrospira, Rhodoplanes, and Sulfuritalea); an apparent decrease in Mycobacterium with potential pathogenicity was observed in DWTR-columns. Regardless, limited denitrification of DWTR-columns was observed as a result of low bioavailability of C in surface water. This finding indicates that DWTR can be used with other methods to ensure denitrification for enhanced treatment effects. Overall, the use of DWTR as an additional medium in column systems can potentially treat eutrophic surface water. Copyright © 2018 Elsevier Ltd. All rights reserved.

  8. Finite-bias electronic transport of molecules in a water solution

    Rungger, Ivan; Chen, X.; Sanvito, Stefano; Schwingenschlö gl, Udo

    2010-01-01

    The effects of water wetting conditions on the transport properties of molecular nanojunctions are investigated theoretically by using a combination of empirical-potential molecular-dynamics and first-principles electronic-transport calculations. These are at the level of the nonequilibrium Green’s-function method implemented for self-interaction corrected density-functional theory. We find that water effectively produces electrostatic gating to the molecular junction with a gating potential determined by the time-averaged water dipole field. Such a field is large for the polar benzene-dithiol molecule, resulting in a transmission spectrum shifted by about 0.6 eV with respect to that of the dry junction. The situation is drastically different for carbon nanotubes (CNTs). In fact, because of their hydrophobic nature the gating is almost negligible so that the average transmission spectrum of wet Au/CNT/Au junctions is essentially the same as that in dry conditions. This suggests that CNTs can be used as molecular interconnects also in water-wet situations, for instance, as tips for scanning tunnel microscopy in solution or in biological sensors.

  9. Finite-bias electronic transport of molecules in a water solution

    Rungger, Ivan

    2010-06-04

    The effects of water wetting conditions on the transport properties of molecular nanojunctions are investigated theoretically by using a combination of empirical-potential molecular-dynamics and first-principles electronic-transport calculations. These are at the level of the nonequilibrium Green’s-function method implemented for self-interaction corrected density-functional theory. We find that water effectively produces electrostatic gating to the molecular junction with a gating potential determined by the time-averaged water dipole field. Such a field is large for the polar benzene-dithiol molecule, resulting in a transmission spectrum shifted by about 0.6 eV with respect to that of the dry junction. The situation is drastically different for carbon nanotubes (CNTs). In fact, because of their hydrophobic nature the gating is almost negligible so that the average transmission spectrum of wet Au/CNT/Au junctions is essentially the same as that in dry conditions. This suggests that CNTs can be used as molecular interconnects also in water-wet situations, for instance, as tips for scanning tunnel microscopy in solution or in biological sensors.

  10. ETV REPORT: REMOVAL OF CHEMICAL CONTAMINANTS IN DRINKING WATER – WATTS PREMIER INC. WP-4V DRINKING WATER TREATMENT SYSTEM

    The Watts Premier WP-4V POU drinking water treatment system was tested for removal of aldicarb, benzene, cadmium, carbofuran, cesium, chloroform, dichlorvos, dicrotophos, fenamiphos, mercury, mevinphos, oxamyl, strontium, and strychnine. The WP-4V employs a reverse osmosis (RO) m...

  11. Removal of calcium and magnesium ions from shale gas flowback water by chemically activated zeolite.

    Chang, Haiqing; Liu, Teng; He, Qiping; Li, Duo; Crittenden, John; Liu, Baicang

    2017-07-01

    Shale gas has become a new sweet spot of global oil and gas exploration, and the large amount of flowback water produced during shale gas extraction is attracting increased attention. Internal recycling of flowback water for future hydraulic fracturing is currently the most effective, and it is necessary to decrease the content of divalent cations for eliminating scaling and maintaining effectiveness of friction reducer. Zeolite has been widely used as a sorbent to remove cations from wastewater. This work was carried out to investigate the effects of zeolite type, zeolite form, activation chemical, activation condition, and sorption condition on removal of Ca 2+ and Mg 2+ from shale gas flowback water. Results showed that low removal of Ca 2+ and Mg 2+ was found for raw zeolite 4A and zeolite 13X, and the efficiency of the mixture of both zeolites was slightly higher. Compared with the raw zeolites, the zeolites after activation using NaOH and NaCl greatly improved the sorption performance, and there was no significant difference between dynamic activation and static activation. Dynamic sorption outperformed static sorption, the difference exceeding 40% and 7-70% for removal of Ca 2+ and Mg 2+ , respectively. Moreover, powdered zeolites outperformed granulated zeolites in divalent cation removal.

  12. Removal of emerging perfluorooctanoic acid and perfluorooctane sulfonate contaminants from lake water.

    Pramanik, Biplob Kumar; Pramanik, Sagor Kumar; Sarker, Dipok Chandra; Suja, Fatihah

    2017-08-01

    Perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) are the major polyfluoroalkyl substances (PFASs) contaminating global water environment. This study investigated the efficiency of granular activated carbon (GAC), ultrafiltration (UF) and nanofiltration (NF) treatment for removing PFOS and PFOA contaminants from lake water. NF gave greater removal of all contaminant types (in terms of organic matter, PFOS and PFOA) than GAC treatment which in turn was greater than UF treatment. The lower removal by UF was due to larger pore size of the membrane compared to the size of the target contaminants. For all treatment processes, lower pH (4) in the feedwater showed greater rejection of the organics and selected PFASs. This was likely due to increase in the electrostatic repulsion between solute and sorbent. It could be observed that on increasing the concentration of organics in the feed solution, the rejection of PFOA/PFOS decreased which was due to competition between organics and PFOS/PFOA for binding sites on the membrane/activated carbon surface. It was also noted that protein content led to greater influence for lower rejection of the PFOA/PFOS than carbohydrate or DOC content. This study demonstrated the potential use of membrane processes for removing emerging persistent organic pollutant removal from lake water.

  13. Removal of emerging contaminants in sewage water subjected to advanced oxidation with ozone.

    Ibáñez, M; Gracia-Lor, E; Bijlsma, L; Morales, E; Pastor, L; Hernández, F

    2013-09-15

    Advanced oxidation processes (AOP) based on ozone treatments, assisted by ultrasounds, have been investigated at a pilot-plant scale in order to evaluate the removal of emerging contaminants in sewage water. Around 60 emerging contaminants, mainly pharmaceuticals from different therapeutically classes and drugs of abuse, have been determined in urban wastewater samples (treated and untreated) by LC-MS/MS. In a first step, the removal efficiency of these contaminants in conventional sewage water treatment plants was evaluated. Our results indicate that most of the compounds were totally or partially removed during the treatment process of influent wastewater. Up to 30 contaminants were quantified in the influent and effluent samples analysed, being antibiotics, anti-inflammatories, cholesterol lowering statin drugs and angiotensin II receptor antagonists the most frequently detected. Regarding drugs of abuse, cocaine and its metabolite benzoylecgonine were the most frequent. In a second step, the effectiveness of AOP in the removal of emerging contaminants remaining in the effluent was evaluated. Ozone treatments have been proven to be highly efficient in the removal, notably decreasing the concentrations for most of the emerging contaminants present in the water samples. The use of ultrasounds, alone or assisting ozone treatments, has been shown less effective, being practically unnecessary. Copyright © 2013 Elsevier B.V. All rights reserved.

  14. Simultaneous removal of water and BTEX from feed gas for a cryogenic plant

    Jones, S.; Lee, S.; Evans, M.; Chen, R.

    1999-07-01

    The removal of water and benzene, toluene, ethyl benzene, xylene (BTEX) from the feed gas of a cryogenic plant is critical in order to avoid precipitation of these components in the cold section of the plant. The design of the Hannibal Gas Plant in Sfax, Tunisia, accomplishes the removal of water and BTEX simultaneously. The plant receives 7.1 million Nm{sub 3}/day of feed gas and produces high heating value pipeline quality sales gas by removing nitrogen in the cold box. A methyl diethanol amine (MDEA) treating system at the front end of the plant is designed to remove carbon dioxide. The glycol system takes the saturated gas from the MDEA contactor and reduces the water content to 7 lb/MMscf. The glycol system is also designed to remove more than half of the BTEX from the feed gas so that these aromatic components will not precipitate in the cold section of the plant. GPA experimental data were used to fit the interaction parameters for the computer simulator used to design the glycol system. The results of the plant performance test verify the validity of the design.

  15. Perchlorate: Health Effects and Technologies for Its Removal from Water Resources

    Thiruvenkatachari Viraraghavan

    2009-04-01

    Full Text Available Perchlorate has been found in drinking water and surface waters in the United States and Canada. It is primarily associated with release from defense and military operations. Natural sources include certain fertilizers and potash ores. Although it is a strong oxidant, perchlorate is very persistent in the environment. At high concentrations perchlorate can affect the thyroid gland by inhibiting the uptake of iodine. A maximum contaminant level has not been set, while a guidance value of 6 ppb has been suggested by Health Canada. Perchlorate is measured in environmental samples primarily by ion chromatography. It can be removed from water by anion exchange or membrane filtration. Biological and chemical processes are also effective in removing this species from water.

  16. Arsenic removal from water using low-cost adsorbents: A comparative study

    Rajaković Ljubinka V.

    2011-01-01

    Full Text Available Inorganic arsenic removal from water using low-cost adsorbents is presented in this paper. Selective removal of As(III and As(V from water was performed with natural materials (zeolite, bentonite, sepiolite, pyrolusite and limonite and industrial by-products (waste filter sand as a water treatment residual and blast furnace slag from steel production; all inexpensive and locally available. Kinetic and equilibrium studies were realized using batch system techniques under conditions that are likely to occur in real water treatment systems. The natural zeolite and the industrial by-products were found to be good and inexpensive sorbents for arsenic while bentonite and sepiolite clays showed little affinity towards arsenic. The highest maximum sorption capacities were obtained for natural zeolite, 4.07 mg As(V g-1, and waste iron slag, 4.04 mg As(V g-1.

  17. Subsurface iron and arsenic removal for shallow tube well drinking water supply in rural Bangladesh.

    van Halem, D; Olivero, S; de Vet, W W J M; Verberk, J Q J C; Amy, G L; van Dijk, J C

    2010-11-01

    Subsurface iron and arsenic removal has the potential to be a cost-effective technology to provide safe drinking water in rural decentralized applications, using existing shallow tube wells. A community-scale test facility in Bangladesh was constructed for injection of aerated water (∼1 m(3)) into an anoxic aquifer with elevated iron (0.27 mmolL(-1)) and arsenic (0.27μmolL(-1)) concentrations. The injection (oxidation) and abstraction (adsorption) cycles were monitored at the test facility and simultaneously simulated in the laboratory with anoxic column experiments. Dimensionless retardation factors (R) were determined to represent the delayed arrival of iron or arsenic in the well compared to the original groundwater. At the test facility the iron removal efficacies increased after every injection-abstraction cycle, with retardation factors (R(Fe)) up to 17. These high removal efficacies could not be explained by the theory of adsorptive-catalytic oxidation, and therefore other ((a)biotic or transport) processes have contributed to the system's efficacy. This finding was confirmed in the anoxic column experiments, since the mechanism of adsorptive-catalytic oxidation dominated in the columns and iron removal efficacies did not increase with every cycle (stable at R(Fe)=∼8). R(As) did not increase after multiple cycles, it remained stable around 2, illustrating that the process which is responsible for the effective iron removal did not promote the co-removal of arsenic. The columns showed that subsurface arsenic removal was an adsorptive process and only the freshly oxidized adsorbed iron was available for the co-adsorption of arsenic. This indicates that arsenic adsorption during subsurface treatment is controlled by the amount of adsorbed iron that is oxidized, and not by the amount of removed iron. For operational purposes this is an important finding, since apparently the oxygen concentration of the injection water does not control the subsurface arsenic

  18. Application of chitosan/polyacrylamide nanofibres for removal of chromate and phosphate in water

    Nthumbi, Richard M.; Catherine Ngila, J.; Moodley, Brenda; Kindness, Andrew; Petrik, Leslie

    Water pollution is an intractable environmental problem in South Africa. Management of the water resource is vital in order to address the water scarcity issues. Research on remediation of contaminated water has focused mainly on the removal of heavy metals such as Pb, Cd, Zn, Hg and Cu and neglected other inorganic pollutants. In this work we focus on the removal of anions, namely chromate and phosphate. Chromium is extensively used in the textile, leather and metallurgy industries and contaminates surface water and groundwater when inadequately treated industrial effluents are discharged. Chromium has been associated with irregular sugar metabolism, nosebleeds and ulcers, and it is also carcinogenic. The phosphate ion is an essential micronutrient responsible for healthy plant growth. However, excess phosphate intake stimulates rapid growth of photosynthetic algae and cyanobacteria, resulting in eutrophication. This phenomenon (algal bloom) causes other organisms to die due to reduced oxygen in the water. In order to offer remediation measures, this study reports the use of electrospun nanofibres for the removal of chromate and phosphate anions. Adsorption experiments were carried out using nanofibres electrospun from chitosan and polyacrylamide polymer blends, cross-linked with glutaraldehyde. Quantification of chromium was done using ICP-OES while UV-Vis spectrophotometry was used for the determination of phosphates. Batch adsorption experiments were done to determine optimum adsorption parameters such as pH, contact time, temperature and initial analyte concentration. Removal of the ions using a flow-adsorption technique through a micro-column was performed. The experimental data obtained were analysed using Langmuir and Freundlich models to study the adsorption mechanisms. The nanofibres had an adsorption capacity for Cr(VI) and PO43- of 0.26 mg g-1 and 392 mg g-1, respectively, and removal efficiencies of 93% and 97.4%, in the same order, in synthetic water

  19. Novel sandwich structure adsorptive membranes for removal of 4-nitrotoluene from water

    Guo, Yuexin [College of Chemistry, Beijing Normal University, Beijing 100875 (China); School of Pharmacy, North China University of Science and Technology, Tangshan 063000 (China); Jia, Zhiqian, E-mail: zhqjia@bnu.edu.cn [College of Chemistry, Beijing Normal University, Beijing 100875 (China)

    2016-11-05

    Highlights: • Novel sandwich PES-SPES/PS-PDVB/PTFE adsorptive membranes were prepared. • The removal efficiency for 4-nitrotoluene is greater than 95% after five recycles. • The membrane showed higher adsorption capacity than that of mixed matrix membrane. - Abstract: Novel sandwich PES-SPES/PS-PDVB/PTFE adsorptive membranes were prepared by a filtration/immersion precipitation method and employed for the removal of 4-nitrotoluene from water. The static adsorption thermodynamics, kinetics, dynamic adsorption/desorption and membrane reusability were investigated. The results showed that the Freundlich model describes the adsorption isotherm satisfactorily. With increased PS-PDVB content, the maximum static adsorption capacity, partition coefficient, apparent adsorption rate constant, and dynamic adsorption capacity all significantly increased. The sandwich membranes showed much higher removal efficiency and adsorption capacity than those of mixed matrix membranes. With respect to dynamics adsorption/desorption, the sandwich membranes exhibited excellent reusability, with a removal efficiency greater than 95% even after five recycles.

  20. Orbiting Water Molecules Dance to Tune Of Galaxy's "Central Engine," Astronomers Say

    2000-01-01

    A disk of water molecules orbiting a supermassive black hole at the core of a galaxy 60 million light-years away is "reverberating" in response to variations in the energy output from the galaxy's powerful "central engine" close to the black hole, astronomers say. The team of astronomers used the National Science Foundation's (NSF) Very Large Array (VLA) radio telescope in New Mexico and the 100-meter-diameter radio telescope of the Max Planck Institute for Radio Astronomy at Effelsberg, Germany, to observe the galaxy NGC 1068 in the constellation Cetus. They announced their findings today at the American Astronomical Society's meeting in Atlanta. The water molecules, in a disk some 5 light-years in diameter, are acting as a set of giant cosmic radio-wave amplifiers, called masers. Using energy radiated by the galaxy's "central engine," the molecules strengthen, or brighten, radio emission at a particular frequency as seen from Earth. "We have seen variations in the radio 'brightness' of these cosmic amplifiers that we believe were caused by variations in the energy output of the central engine," said Jack Gallimore, an astronomer at the National Radio Astronomy Observatory (NRAO) in Charlottesville, VA. "This could provide us with a valuable new tool for learning about the central engine itself," he added. Gallimore worked with Stefi Baum of the Space Telescope Science Institute in Baltimore, MD; Christian Henkel of the Max Planck Institute for Radio Astronomy in Bonn, Germany; Ian Glass of the South African Astronomical Observatory; Mark Claussen of the NRAO in Socorro, NM; and Almudena Prieto of the European Southern Observatory in Munich, Germany. "Our observations show that NGC 1068 is the second-known case of a giant disk of water molecules orbiting a supermassive black hole at a galaxy's core," Gallimore said. The first case was the galaxy NGC 4258 (Messier 106), whose disk of radio-amplifying water molecules was measured by the NSF's Very Long Baseline

  1. Removal of lead and zinc ions from water by low cost adsorbents.

    Mishra, P C; Patel, R K

    2009-08-30

    In this study, activated carbon, kaolin, bentonite, blast furnace slag and fly ash were used as adsorbent with a particle size between 100 mesh and 200 mesh to remove the lead and zinc ions from water. The concentration of the solutions prepared was in the range of 50-100 mg/L for lead and zinc for single and binary systems which are diluted as required for batch experiments. The effect of contact time, pH and adsorbent dosage on removal of lead and zinc by adsorption was investigated. The equilibrium time was found to be 30 min for activated carbon and 3h for kaolin, bentonite, blast furnace slag and fly ash. The most effective pH value for lead and zinc removal was 6 for activated carbon. pH value did not effect lead and zinc removal significantly for other adsorbents. Adsorbent doses were varied from 5 g/L to 20 g/L for both lead and zinc solutions. An increase in adsorbent doses increases the percent removal of lead and zinc. A series of isotherm studies was undertaken and the data evaluated for compliance was found to match with the Langmuir and Freundlich isotherm models. To investigate the adsorption mechanism, the kinetic models were tested, and it follows second order kinetics. Kinetic studies reveals that blast furnace slag was not effective for lead and zinc removal. The bentonite and fly ash were effective for lead and zinc removal.

  2. Removal of Heavy Metals from Drinking Water by Magnetic Carbon Nanostructures Prepared from Biomass

    Muneeb Ur Rahman Khattak, Muhammad; Zahoor, Muhammad; Muhammad, Bakhtiar; Khan, Farhat Ali; Ullah, Riaz; AbdEI-Salam, Naser M.

    2017-01-01

    Heavy metals contamination of drinking water has significant adverse effects on human health due to their toxic nature. In this study a new adsorbent, magnetic graphitic nanostructures were prepared from watermelon waste. The adsorbent was characterized by different instrumental techniques (surface area analyzer, FTIR, XRD, EDX, SEM, and TG/DTA) and was used for the removal of heavy metals (As, Cr, Cu, Pb, and Zn) from water. The adsorption parameters were determined for heavy metals adsorpti...

  3. Oil palm biomass-based adsorbents for the removal of water pollutants--a review.

    Ahmad, Tanweer; Rafatullah, Mohd; Ghazali, Arniza; Sulaiman, Othman; Hashim, Rokiah

    2011-07-01

    This article presents a review on the role of oil palm biomass (trunks, fronds, leaves, empty fruit bunches, shells, etc.) as adsorbents in the removal of water pollutants such as acid and basic dyes, heavy metals, phenolic compounds, various gaseous pollutants, and so on. Numerous studies on adsorption properties of various low-cost adsorbents, such as agricultural wastes and its based activated carbons, have been reported in recent years. Studies have shown that oil palm-based adsorbent, among the low-cost adsorbents mentioned, is the most promising adsorbent for removing water pollutants. Further, these bioadsorbents can be chemically modified for better efficiency and can undergo multiple reuses to enhance their applicability at an industrial scale. It is evident from a literature survey of more than 100 recent papers that low-cost adsorbents have demonstrated outstanding removal capabilities for various pollutants. The conclusion is been drawn from the reviewed literature, and suggestions for future research are proposed.

  4. Removal of decay heat by specially designed isolation condensers for advanced heavy water reactors

    Dhawan, M L; Bhatia, S K [Reactor Engineering Division, Bhabha Atomic Research Centre, Mumbai (India)

    1994-06-01

    For Advanced Heavy Water Reactor (AHWR), removal of decay heat and containment heat is being considered by passive means. For this, special type of isolation condensers are designed. Isolation condensers when submerged in a pool of water, are the best choice because condensation of high temperature steam is an extremely efficient heat transfer mechanism. By the use of isolation condensers, not only heat is removed but also pressure and temperature of the system are automatically controlled without losing the coolant and without using conventional safety relief valves. In this paper, design optimisation studies of isolation condensers of different types with natural circulation for the removal of core decay heat for AHWR is presented. (author). 8 refs., 2 figs.

  5. Chitosan membrane development and design of equipment for the removal of heavy metals from water

    Mora Molina, Jesus; Chaves Barquero, Luis; Araya Marchena, Mario; Starbird Perez, Ricardo

    2012-01-01

    A filtration technique has compared with 1,75% m/v chitosan membranes, crosslinked with glutaraldehyde (0,08% m/v) and without cross link, to quantify the removal capacity of chromium, copper and cadmium ions of model solutions. In addition, a simple and low cost equipment was developed to use with prepared membranes. The main goal has been to use biodegradable materials for removing heavy metals from water, through a low energy consumption, cheap, and applicable to specific problems. Two data sheets were prepared for the membranes and was found that chromium was the metal with the highest removal from water, by using a crosslinked membrane. Metal adsorption was best adjusted to the Freundlich isotherm model, better than Langmuir isotherm model. However, no correlation has been found between pore size of the membranes and crosslinking degree. (author) [es

  6. Chitosan membrane development and design of equipment for the removal of heavy metals from water

    Mora Molina, Jesus; Starbird Perez, Ricardo; Chaves Barquero, Luis; Araya Marchena, Mario

    2011-01-01

    A filtration technique has compared with 1,75% m/v chitosan membranes, crosslinked with glutaraldehyde (0,08% m/v) and without cross link, to quantify the removal capacity of chromium, copper and cadmium ions of model solutions. In addition, a simple and low cost equipment was developed to use with prepared membranes. The main goal has been to use biodegradable materials for removing heavy metals from water, through a low energy consumption, cheap, and applicable to specific problems. Two data sheets were prepared for the membranes and was found that chromium was the metal with the highest removal from water, by using a crosslinked membrane. Metal adsorption was best adjusted to the Freundlich isotherm model, better than Langmuir isotherm model. However, no correlation has been found between pore size of the membranes and crosslinking degree. (author) [es

  7. Arsenic removal methods for drinking water in the developing countries: technological developments and research needs.

    Kabir, Fayzul; Chowdhury, Shakhawat

    2017-11-01

    Arsenic pollution of drinking water is a concern, particularly in the developing countries. Removal of arsenic from drinking water is strongly recommended. Despite the availability of efficient technologies for arsenic removal, the small and rural communities in the developing countries are not capable of employing most of these technologies due to their high cost and technical complexity. There is a need for the "low-cost" and "easy to use" technologies to protect the humans in the arsenic affected developing countries. In this study, arsenic removal technologies were summarized and the low-cost technologies were reviewed. The advantages and disadvantages of these technologies were identified and their scopes of applications and improvements were investigated. The costs were compared in context to the capacity of the low-income populations in the developing countries. Finally, future research directions were proposed to protect the low-income populations in the developing countries.

  8. Removal of Perfluorinated Compounds From Water using Nanoscale Zero-Valent Iron

    Arvaniti, Olga S.; Hwang, Yuhoon; Andersen, Henrik Rasmus

    Perfluorinated Compounds (PFCs) are persistent micropollutants that have been detected in various environmental and biological matrices, worldwide. During the last decade, these compounds have also been detected in municipal wastewater and tap water. Due to the stability of C-F bond......, the application of biological and conventional physicochemical treatment methods does not seem to remove sufficient these compounds from water and wastewater. In the current study, the removal efficiency of four PFCs using three different types of nanoscale zero-valent iron (nZVI) was investigated. Influencing...... factors such as, initial pH solution, reaction temperature and nZVI dosage were also studied. According to the results, target compounds were removed in the presence of chemically synthesized nZVI modified with Mg-aminoclay (MgAC) than under commercial iron powder and chemically synthesized uncoated n...

  9. Relationship between diffusivity of water molecules inside hydrating tablets and their drug release behavior elucidated by magnetic resonance imaging.

    Kikuchi, Shingo; Onuki, Yoshinori; Kuribayashi, Hideto; Takayama, Kozo

    2012-01-01

    We reported previously that sustained release matrix tablets showed zero-order drug release without being affected by pH change. To understand drug release mechanisms more fully, we monitored the swelling and erosion of hydrating tablets using magnetic resonance imaging (MRI). Three different types of tablets comprised of polyion complex-forming materials and a hydroxypropyl methylcellulose (HPMC) were used. Proton density- and diffusion-weighted images of the hydrating tablets were acquired at intervals. Furthermore, apparent self-diffusion coefficient maps were generated from diffusion-weighted imaging to evaluate the state of hydrating tablets. Our findings indicated that water penetration into polyion complex tablets was faster than that into HPMC matrix tablets. In polyion complex tablets, water molecules were dispersed homogeneously and their diffusivity was relatively high, whereas in HPMC matrix tablets, water molecule movement was tightly restricted within the gel. An optimal tablet formulation determined in a previous study had water molecule penetration and diffusivity properties that appeared intermediate to those of polyion complex and HPMC matrix tablets; water molecules were capable of penetrating throughout the tablets and relatively high diffusivity was similar to that in the polyion complex tablet, whereas like the HPMC matrix tablet, it was well swollen. This study succeeded in characterizing the tablet hydration process. MRI provides profound insight into the state of water molecules in hydrating tablets; thus, it is a useful tool for understanding drug release mechanisms at a molecular level.

  10. Carbonate effects on hexavalent uranium removal from water by nanocrystalline titanium dioxide

    Wazne, Mahmoud; Meng, Xiaoguang; Korfiatis, George P.; Christodoulatos, Christos

    2006-01-01

    A novel nanocrystalline titanium dioxide was used to treat depleted uranium (DU)-contaminated water under neutral and alkaline conditions. The novel material had a total surface area of 329 m 2 /g, total surface site density of 11.0 sites/nm 2 , total pore volume of 0.415 cm 3 /g and crystallite size of 6.0 nm. It was used in batch tests to remove U(VI) from synthetic solutions and contaminated water. However, the capacity of the nanocrystalline titanium dioxide to remove U(VI) from water decreased in the presence of inorganic carbonate at pH > 6.0. Adsorption isotherms, Fourier transform infrared (FTIR) spectroscopy, and surface charge measurements were used to investigate the causes of the reduced capacity. The surface charge and the FTIR measurements suggested that the adsorbed U(VI) species was not complexed with carbonate at neutral pH values. The decreased capacity of titanium dioxide to remove U(VI) from water in the presence of carbonate at neutral to alkaline pH values was attributed to the aqueous complexation of U(VI) by inorganic carbonate. The nanocrystalline titanium dioxide had four times the capacity of commercially available titanium dixoide (Degussa P-25) to adsorb U(VI) from water at pH 6 and total inorganic carbonate concentration of 0.01 M. Consequently, the novel material was used to treat DU-contaminated water at a Department of Defense (DOD) site

  11. Removal of two antibacterial compounds triclocarban and triclosan in a waste water treatment plant

    This study investigates the fate of Triclocarban (TCC) and Triclosan (TCS) in a waste water treatment plant (WWTP). Our goal was to identify the most effective removal step and to determine the amount on the solid phase versus degraded. Our influent contained higher TCS than TCC concentrations (8....

  12. Synthesis and characterization of a mesoporous hydrous zirconium oxide used for arsenic removal from drinking water

    Bortun, Anatoly; Bortun, Mila; Pardini, James; Khainakov, Sergei A.; Garcia, Jose R.

    2010-01-01

    Powder (20-50 μm) mesoporous hydrous zirconium oxide was prepared from a zirconium salt granular precursor. The effect of some process parameters on product morphology, porous structure and adsorption performance has been studied. The use of hydrous zirconium oxide for selective arsenic removal from drinking water is discussed.

  13. REMOVAL OF MTBE FROM WATER BY MEMBRANE-BASED PERVAPORATION TECHNOLOGY

    The ability of pervaporation to remove methyl t-butyl ether (MTBE) from water has been evaluated at both bench- and pilot-scales. In pervaporation, a liquid stream containing two or more components is placed in contact with one side of a non-porous polymeric membrane while a vac...

  14. Fluoride Removal From Drinking Water by Electrocoagulation Using Iron and Aluminum Electrodes

    Takdastan

    2014-07-01

    Full Text Available Background Existence of fluoride in drinking water above the permissible level causes human skeletal fluorosis. Objectives Electrocoagulation by iron and aluminum electrodes was proposed for removing fluoride from drinking water. Materials and Methods Effects of different operating conditions such as treatment time, initial pH, applied voltage, type and number of electrodes, the spaces between aluminum and iron electrodes, and energy consumption during electrocoagulation were investigated in the batch reactor. Variable concentrations of fluoride solution were prepared by mixing proper amounts of sodium fluoride with deionized water. Results Experimental results showed that aluminum electrode is more effective in fluoride removal than iron, as in 40 minutes and initial pH of 7.5 at 20 V, the fluoride removal process reached to 97.86%. The final recommendable limit of fluoride (1.5 mg/L was obtained in 10 minutes at 20 V with the aluminum electrode. Conclusions In electrocoagulation with iron and aluminum electrodes, increase of voltage, number of electrodes and reaction time as well as decrease of the spaces between electrodes, enhanced the fluoride removal efficiency from drinking water. In addition the effect of pH and initial concentration of fluoride varied with types of electrodes.

  15. Removal of geosmin and 2-methylisorboneol (2-MIB) in water from ...

    Geosmin and 2-methylisorboneol (2-MIB) are major organic pollutants ... The use of granular activated carbon (GAC) in the removal of geosmin and 2-MIB is ... were extracted from water samples by solid phase micro-extraction (SPME) and ...

  16. Multi-weight isotherm results for mercury removal in upper East Fork Popular Creek water

    Bostick, D.A.; Klasson, K.T.

    1998-02-01

    Many sorbents have been developed for the removal of mercury and heavy metals from waters; however, the majority of data published to date do not address the removal of mercury to the target levels represented in this project. The application to which these sorbents are targeted for use is the removal of mercury from microgram-per-liter levels to low nanogram-per-liter levels. Sorbents with thiouronium, thiol, amine, sulfur, and proprietary functional groups were selected for these studies. The initial mercury content in the majority of the batch samples was significantly augmented so that the equilibrium concentration was similar to that found in the original stream sample for at least one sample. Mercury was successfully removed from actual water via adsorption onto Ionac SR-4 (by Sybron Chemicals, Inc.), Keyle:X (by SolmeteX), and Mersorb (by Nucon International, Inc.) resins to levels below the target goal of 12 ng/L. A thiol-based resin (Ionac SR-4) performed the best, indicating that over 200,000 volumes of water could be treated with one volume of resin. The cost of the resin is approximately $0.24 per 1000 gal of water

  17. Aging assessment of Residual Heat Removal systems in Boiling Water Reactors

    Lofaro, R.J.; Aggarwal, S.

    1992-01-01

    The effects of aging on Residual Heat Removal systems in Boiling Water Reactors have been studied as part of the Nuclear Plant Aging Research Program. The aging phenomena has been characterized by analyzing operating experience from various national data bases. In addition, actual plant data was obtained to supplement and validate the data base findings

  18. Arsenic removal by coagulation using ferric chloride and chitosan from water

    Farid Hesami

    2013-01-01

    Conclusions: Chitosan as natural coagulant aid improved arsenic removal efficiency by coagulation process using FeCl 3 . This method can be used for regions with drinking water contaminated with initial arsenic concentration less than 1 000 μg/l.

  19. Multifunctional Silver Coated E-33/Iron Oxide Water Filters: Inhibition of Biofilm Growth and Arsenic Removal

    Bayoxide® E33 (E-33, Goethite) is a widely used commercial material for arsenic adsorption. It is a mixture of iron oxyhydroxide and oxides. E-33 is primarily used to remove arsenic from water and to a lesser extent, other anions, but generally lacks multifunctuality. It is a non...

  20. ARSENIC REMOVAL FROM DRINKING WATER BY ION EXCHANGE AND ACTIVATED ALUMINA PLANTS

    This report documents a long term performance study of two ion exchange (IE) and two activated alumina (AA) treatment plants to remove arsenic from drinking water. Performance information was collected on these systems that are located in the northeast for one full year. The stud...