WorldWideScience

Sample records for aqueous liquid waste

  1. Investigation and development of liquid-liquid extraction systems for the removal of pertechnetate from aqueous nuclear waste stream simulants

    Science.gov (United States)

    Gansle, Kristina Marie Rohal

    1998-11-01

    The solvent extraction behavior of perrhenate (ReO 4-) and pertechnetate (TcO4- ) from aqueous nuclear waste stream simulants was examined using the anion-exchange reagent Aliquat-336 nitrate. The extraction tendencies of ReO 4- followed those of TcO4- from both acidic and basic media, demonstrating that ReO4 - was a suitable nonradioactive surrogate for TcO4 -. For ICP-AES analysis of Re in high salt solutions, a V-groove nebulizer and 1:1 dilution of the sample and standards with 0.1% Triton X-100 surfactant reduced deposition of solids within the sample introduction system, thus minimizing memory effects. A new approach to waste remediation technology, Redox-Recyclable Extraction and Recovery (R2ER), was also studied. The redox-active species 1,1',3,3'-tetrakis(2-methyl-2-hexyl)ferrocene (HEP) was oxidized to its cationic form for extraction of TcO4 - or ReO4- from aqueous waste and reduced to its neutral form for recovery of the anion. The thermodynamics of liquid-liquid interfacial electron transfer for the oxidation/activation of HEP were shown to be controlled by three factors: the reduction potentials of the redox-active species in the aqueous and organic phases and the transfer of an ion across the liquid-liquid interface. The deactivation/reduction rate of HEP+NO3- by iron was affected by organic solvent diluent and improved by treating the iron with hexanes and 1 M HCl. The volume of solid secondary-waste in the R2ER cycle was reduced by a factor of 3000. In complete extraction/recovery cycles, HEP+NO3- in 2-nonanone removed greater than 99% TcO4- from the 101-SY, 103-SY, 1 M HCl and 1 M NaOH/1.5 M NaNO3 Hanford Tank waste simulants. Another redox-active extractant, bis(hydridotris(1-pyrazolyl)borato)iron(III) nitrate (FeTp2+NO3-), was also selective for ReO4- remediation from simulated aqueous waste. Organic solutions of the alkyl substituted ferricenium extractants were not stable in the presence of nucleophilic anions and/or reducing agents. HEP+NO3

  2. Liquid secondary waste. Waste form formulation and qualification

    Energy Technology Data Exchange (ETDEWEB)

    Cozzi, A. D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Dixon, K. L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Hill, K. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); King, W. D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Nichols, R. L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-03-01

    The Hanford Site Effluent Treatment Facility (ETF) currently treats aqueous waste streams generated during Site cleanup activities. When the Hanford Tank Waste Treatment and Immobilization Plant (WTP) begins operations, a liquid secondary waste (LSW) stream from the WTP will need to be treated. The volume of effluent for treatment at the ETF will increase significantly. Washington River Protection Solutions is implementing a Secondary Liquid Waste Immobilization Technology Development Plan to address the technology needs for a waste form and solidification process to treat the increased volume of waste planned for disposal at the Integrated Disposal Facility IDF). Waste form testing to support this plan is composed of work in the near term to demonstrate the waste form will provide data as input to a performance assessment (PA) for Hanford’s IDF.

  3. Extraction of Theanine from Waste Liquid of Tea Polyphenol Production in Aqueous Two-phase Systems with Cationic and Anionic Surfactants

    Institute of Scientific and Technical Information of China (English)

    ZHANG Junwei; WANG Yan; PENG Qijun

    2013-01-01

    Extraction of theanine from waste liquid of tea polyphenol production was studied in aqueous surfactant two-phase system (ASTP) with cationic suffactant (CTAB) and anionic surfactant (SDS).Results indicate that the region of ASTP is narrow and there is only a two-phase region of cationic surfactant.The increase in concentrations of NaBr and Na2SO4 are beneficial to the formation of ASTP.Theanine concentration in the bottom phase increases with increasing concentration of theanine,whereas the partition coefficient and extraction rate only change a little when the concentration of theanine is above 0.2 g· L-1.With the increase of SDS concentration,the phase ratio and the partition coefficient decrease,while the extraction efficiency of theanine increases and the concentration of theaninc changes a little in the range from 2.4/7.5 to 2.8/7.2 for SDS/CTAB ratio.The temperature has a notable effect on the concentration of theanine in the bottom phase,partition coefficient and extraction rate of theanine.The increase of waste liquid decreases the phase ratio,increases the concentration and extraction rate of theanine in the bottom phase,since the protein and the saccharide enter the bottom phase with theanine.

  4. Bioprocessing of a stored mixed liquid waste

    Energy Technology Data Exchange (ETDEWEB)

    Wolfram, J.H.; Rogers, R.D. [Idaho National Engineering Lab., Idaho Falls, ID (United States); Finney, R. [Mound Applied Technologies, Miamisburg, OH (United States)] [and others

    1995-12-31

    This paper describes the development and results of a demonstration for a continuous bioprocess for mixed waste treatment. A key element of the process is an unique microbial strain which tolerates high levels of aromatic solvents and surfactants. This microorganism is the biocatalysis of the continuous flow system designed for the processing of stored liquid scintillation wastes. During the past year a process demonstration has been conducted on commercial formulation of liquid scintillation cocktails (LSC). Based on data obtained from this demonstration, the Ohio EPA granted the Mound Applied Technologies Lab a treatability permit allowing the limited processing of actual mixed waste. Since August 1994, the system has been successfully processing stored, {open_quotes}hot{close_quotes} LSC waste. The initial LSC waste fed into the system contained 11% pseudocumene and detectable quantities of plutonium. Another treated waste stream contained pseudocumene and tritium. Data from this initial work shows that the hazardous organic solvent, and pseudocumene have been removed due to processing, leaving the aqueous low level radioactive waste. Results to date have shown that living cells are not affected by the dissolved plutonium and that 95% of the plutonium was sorbed to the biomass. This paper discusses the bioprocess, rates of processing, effluent, and the implications of bioprocessing for mixed waste management.

  5. Aqueous Corrosion Rates for Waste Package Materials

    Energy Technology Data Exchange (ETDEWEB)

    S. Arthur

    2004-10-08

    The purpose of this analysis, as directed by ''Technical Work Plan for: Regulatory Integration Modeling and Analysis of the Waste Form and Waste Package'' (BSC 2004 [DIRS 171583]), is to compile applicable corrosion data from the literature (journal articles, engineering documents, materials handbooks, or standards, and national laboratory reports), evaluate the quality of these data, and use these to perform statistical analyses and distributions for aqueous corrosion rates of waste package materials. The purpose of this report is not to describe the performance of engineered barriers for the TSPA-LA. Instead, the analysis provides simple statistics on aqueous corrosion rates of steels and alloys. These rates are limited by various aqueous parameters such as temperature (up to 100 C), water type (i.e., fresh versus saline), and pH. Corrosion data of materials at pH extremes (below 4 and above 9) are not included in this analysis, as materials commonly display different corrosion behaviors under these conditions. The exception is highly corrosion-resistant materials (Inconel Alloys) for which rate data from corrosion tests at a pH of approximately 3 were included. The waste package materials investigated are those from the long and short 5-DHLW waste packages, 2-MCO/2-DHLW waste package, and the 21-PWR commercial waste package. This analysis also contains rate data for some of the materials present inside the fuel canisters for the following fuel types: U-Mo (Fermi U-10%Mo), MOX (FFTF), Thorium Carbide and Th/U Carbide (Fort Saint Vrain [FSVR]), Th/U Oxide (Shippingport LWBR), U-metal (N Reactor), Intact U-Oxide (Shippingport PWR, Commercial), aluminum-based, and U-Zr-H (TRIGA). Analysis of corrosion rates for Alloy 22, spent nuclear fuel, defense high level waste (DHLW) glass, and Titanium Grade 7 can be found in other analysis or model reports.

  6. Advanced methods for the treatment of organic aqueous wastes: wet air oxidation and wet peroxide oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Debellefontaine, Hubert; Chakchouk, Mehrez; Foussard, Jean Noel [Institut National des Sciences Appliquees (INSA), 31 - Toulouse (France). Dept. de Genie des Procedes Industriels; Tissot, Daniel; Striolo, Phillipe [IDE Environnement S.A., Toulouse (France)

    1993-12-31

    There is a growing concern about the problems of wastes elimination. Various oxidation techniques are suited for elimination of organic aqueous wastes, however, because of the environmental drawbacks of incineration, liquid phase oxidation should be preferred. `Wet Air Oxidation` and `Wet Peroxide Oxidation`are alternative processes which are discussed in this paper. 17 refs., 13 figs., 4 tabs.

  7. Aqueous extraction of pectin from sisal waste.

    Science.gov (United States)

    Santos, Jener David G; Espeleta, Alexandre F; Branco, Alexsandro; de Assis, Sandra A

    2013-02-15

    In this work, sisal waste was used as a source of pectin. Sisal is known worldwide as a source of hard fibres, and Brazil is the largest producer of sisal, producing more than 246,000 tonnes. However, the process of removing the fibres of the sisal leaf generates 95% waste. This study investigated the effect of the liquid/solid ratio (%), time (min), and temperature (°C) on the yield of the pectin obtained from sisal waste by attractive environmentally friendly process. A statistical Box-Behnken design was applied to determine the important effects and interactions of these independent variables on the yield of pectin, the dependent variable. Significant models were obtained. The yield of the extracted pectin ranged from 4.61 to 19.2%. The conditions that produced the highest yield (19.2%) were a temperature of 85 °C, extraction time of 60 min and a liquid/solid ratio of 2%.

  8. Aqueous Solutions of Ionic Liquids: Microscopic Assembly.

    Science.gov (United States)

    Vicent-Luna, Jose Manuel; Dubbeldam, David; Gómez-Álvarez, Paula; Calero, Sofia

    2016-02-01

    Aqueous solutions of ionic liquids are of special interest, due to the distinctive properties of ionic liquids, in particular, their amphiphilic character. A better understanding of the structure-property relationships of such systems is hence desirable. One of the crucial molecular-level interactions that influences the macroscopic behavior is hydrogen bonding. In this work, we conduct molecular dynamics simulations to investigate the effects of ionic liquids on the hydrogen-bond network of water in dilute aqueous solutions of ionic liquids with various combinations of cations and anions. Calculations are performed for imidazolium-based cations with alkyl chains of different lengths and for a variety of anions, namely, [Br](-), [NO3](-), [SCN](-) [BF4](-), [PF6](-), and [Tf2N](-). The structure of water and the water-ionic liquid interactions involved in the formation of a heterogeneous network are analyzed by using radial distribution functions and hydrogen-bond statistics. To this end, we employ the geometric criterion of the hydrogen-bond definition and it is shown that the structure of water is sensitive to the amount of ionic liquid and to the anion type. In particular, [SCN](-) and [Tf2N](-) were found to be the most hydrophilic and hydrophobic anions, respectively. Conversely, the cation chain length did not influence the results.

  9. Electrochemical treatment of liquid wastes

    Energy Technology Data Exchange (ETDEWEB)

    Hobbs, D.T. [Savannah River Technology Center, Aiken, SC (United States)

    1997-10-01

    Under this task, electrochemical treatment processes are being evaluated and developed for the destruction of organic compounds and nitrates/nitrites and the removal of other hazardous species from liquid wastes stored throughout the DOE complex. This technology targets the (1) destruction of nitrates, nitrites and organic compounds; (2) removal of radionuclides; and (3) removal of RCRA metals. The development program consists of five major tasks: (1) evaluation of electrochemical reactors for the destruction and removal of hazardous waste components, (2) development and validation of engineering process models, (3) radioactive laboratory-scale tests, (4) demonstration of the technology in an engineering-scale reactor, and (5) analysis and evaluation of test data. The development program team is comprised of individuals from national laboratories, academic institutions, and private industry. Possible benefits of this technology include: (1) improved radionuclide separation as a result of the removal of organic complexants, (2) reduction in the concentrations of hazardous and radioactive species in the waste (e.g., removal of nitrate, mercury, chromium, cadmium, {sup 99}Tc, and {sup 106}Ru), (3) reduction in the size of the off-gas handling equipment for the vitrification of low-level waste (LLW) by reducing the source of NO{sub x} emissions, (4) recovery of chemicals of value (e.g. sodium hydroxide), and (5) reduction in the volume of waste requiring disposal.

  10. Supported liquid inorganic membranes for nuclear waste separation

    Energy Technology Data Exchange (ETDEWEB)

    Bhave, Ramesh R; DeBusk, Melanie M; DelCul, Guillermo D; Delmau, Laetitia H; Narula, Chaitanya K

    2015-04-07

    A system and method for the extraction of americium from radioactive waste solutions. The method includes the transfer of highly oxidized americium from an acidic aqueous feed solution through an immobilized liquid membrane to an organic receiving solvent, for example tributyl phosphate. The immobilized liquid membrane includes porous support and separating layers loaded with tributyl phosphate. The extracted solution is subsequently stripped of americium and recycled at the immobilized liquid membrane as neat tributyl phosphate for the continuous extraction of americium. The sequestered americium can be used as a nuclear fuel, a nuclear fuel component or a radiation source, and the remaining constituent elements in the aqueous feed solution can be stored in glassified waste forms substantially free of americium.

  11. Electrochemical treatment of liquid wastes

    Energy Technology Data Exchange (ETDEWEB)

    Hobbs, D.

    1996-10-01

    Electrochemical treatment processes are being evaluated and developed for the destruction of organic compounds and nitrates/nitrites and the removal of other hazardous species from liquid wastes stored throughout the DOE complex. This activity consists of five major tasks: (1) evaluation of different electrochemical reactors for the destruction and removal of hazardous waste components, (2) development and validation of engineering process models, (3) radioactive laboratory-scale tests, (4) demonstration of the technology in an engineering-scale size reactor, and (5) analysis and evaluation of testing data. The development program team is comprised of individuals from federal, academic, and private industry. Work is being carried out in DOE, academic, and private industrial laboratories.

  12. Batch liquid-liquid extraction of phenol from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Palma, M.S.A.; Shibata, C. [Department of Biochemical Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, University of Sao Paulo, Sao Paulo-SP (Brazil); Paiva, J.L. [Department of Chemical Engineering, Polytechnical School, University of Sao Paulo, Sao Paulo-SP (Brazil); Zilli, M. [Department of Chemical and Process Engineering, University of Genoa, Genoa (Italy); Converti, A.

    2010-01-15

    The aim of this work is the study of batch liquid-liquid extraction of phenol from aqueous solutions in a bench-scale well-mixed reactor. The influence of the ratio of phase volumes, temperature, and rotational speed on phenol removal (0.72-1.1 % w/w) was investigated using methyl isobutyl ketone as an extracting solvent. For this purpose, the ratio of phase volumes were set at 0.1 and 0.2, the temperature at 10, 20, and 30 C, and the rotational speed at 300, 400, and 500 rpm. A physical model based on the material balance of the phases as well as the equation of mass flux between the phases allowed the estimation of the overall coefficient of mass transfer coupled with the superficial area. Moreover, it proved to fit, satisfactorily well, the experimental data of residual phenol concentration in the organic phase versus time under all the conditions investigated. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  13. Solid and Liquid Waste Drying Bag

    Science.gov (United States)

    Litwiller, Eric (Inventor); Hogan, John A. (Inventor); Fisher, John W. (Inventor)

    2009-01-01

    Method and system for processing waste from human activities, including solids, liquids and vapors. A fluid-impermeable bag, lined with a liquid-impermeable but vapor-permeable membrane, defining an inner bag, is provided. A vacuum force is provided to extract vapors so that the waste is moved toward a selected region in the inner bag, extracted vapors, including the waste vapors and vaporized portions of the waste liquids are transported across the membrane, and most or all of the solids remain within the liner. Extracted vapors are filtered, and sanitized components thereof are isolated and optionally stored. The solids remaining within the liner are optionally dried and isolated for ultimate disposal.

  14. Treatment of mixed radioactive liquid wastes at Argonne National Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Vandegrift, G.F.; Chamberlain, D.B.; Conner, C. [and others

    1994-03-01

    Aqueous mixed waste at Argonne National Laboratory (ANL) is traditionally generated in small volumes with a wide variety of compositions. A cooperative effort at ANL between Waste Management (WM) and the Chemical Technology Division (CMT) was established, to develop, install, and implement a robust treatment operation to handle the majority of such wastes. For this treatment, toxic metals in mixed-waste solutions are precipitated in a semiautomated system using Ca(OH){sub 2} and, for some metals, Na{sub 2}S additions. This step is followed by filtration to remove the precipitated solids. A filtration skid was built that contains several filter types which can be used, as appropriate, for a variety of suspended solids. When supernatant liquid is separated from the toxic-metal solids by decantation and filtration, it will be a low-level waste (LLW) rather than a mixed waste. After passing a Toxicity Characteristic Leaching Procedure (TCLP) test, the solids may also be treated as LLW.

  15. Removal of fluoride ions from aqueous solution by waste mud

    Energy Technology Data Exchange (ETDEWEB)

    Kemer, Baris; Ozdes, Duygu; Gundogdu, Ali; Bulut, Volkan N.; Duran, Celal [Karadeniz Technical University, Faculty of Arts and Sciences, Department of Chemistry, 61080 Trabzon (Turkey); Soylak, Mustafa, E-mail: soylak@erciyes.edu.tr [Erciyes University, Faculty of Arts and Sciences, Department of Chemistry, 38039 Kayseri (Turkey)

    2009-09-15

    The present study was carried out to assess the ability of original waste mud (o-WM) and different types of activated waste mud which are acid-activated (a-WM) and precipitated waste mud (p-WM), in order to remove excess of fluoride from aqueous solution by using batch technique. The p-WM exhibited greater performance than the others. Adsorption studies were conducted as a function of pH, contact time, initial fluoride concentration, adsorbent concentration, temperature, etc. Studies were also performed to understand the effect of some co-existing ions present in aqueous solutions. Adsorption process was found to be almost independent of pH for all types of waste mud. Among the kinetic models tested for p-WM, pseudo-second-order model fitted the kinetic data well with a perfect correlation coefficient value of 1.00. It was found that the adequate time for the adsorption equilibrium of fluoride was only 1 h. Thermodynamic parameters including the Gibbs free energy ({Delta}G{sup o}), enthalpy ({Delta}H{sup o}), and entropy ({Delta}S{sup o}) revealed that adsorption of fluoride ions on the p-WM was feasible, spontaneous and endothermic in the temperature range of 0-40 deg. C. Experimental data showed a good fit with the Langmuir and Freundlich adsorption isotherm models. Results of this study demonstrated the effectiveness and feasibility of WM for removal of fluoride ions from aqueous solution.

  16. 40 CFR 761.269 - Sampling liquid PCB remediation waste.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Sampling liquid PCB remediation waste..., AND USE PROHIBITIONS Cleanup Site Characterization Sampling for PCB Remediation Waste in Accordance with § 761.61(a)(2) § 761.269 Sampling liquid PCB remediation waste. (a) If the liquid is single...

  17. BIOGAS PRODUCTION FROM TOFU LIQUID WASTE ON TREATED AGRICULTURAL WASTES

    OpenAIRE

    Budy Rahmat; Tedi Hartoyo; Yaya Sunarya

    2014-01-01

    The Tofu Liquid Waste (TLW) as a pollution might be processed into biogas which was environmentally friendly and had potential to replace burning wood or oil. However, the waste could not directly be employed as the biogas substrate due to the high nitrogen content which was not suitable to the methanogen microorganism on the biogas digester and did not produce biogas. It was therefore necessary to adapt the carbon-nitrogen ratio in TLW with the addition of other organic materials that had a ...

  18. Liquid Secondary Waste Grout Formulation and Waste Form Qualification

    Energy Technology Data Exchange (ETDEWEB)

    Um, Wooyong [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Williams, B. D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Snyder, Michelle M. V. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Wang, Guohui [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2016-05-23

    This report describes the results from liquid secondary waste (LSW) grout formulation and waste form qualification tests performed at Pacific Northwest National Laboratory (PNNL) for Washington River Protection Solutions (WRPS) to evaluate new formulations for preparing a grout waste form with high-sulfate secondary waste simulants and the release of key constituents from these grout monoliths. Specific objectives of the LSW grout formulation and waste form qualification tests described in this report focused on five activities: 1.preparing new formulations for the LSW grout waste form with high-sulfate LSW simulants and solid characterization of the cured LSW grout waste form 2.conducting the U.S. Environmental Protection Agency (EPA) Method 1313 leach test (EPA 2012) on the grout prepared with the new formulations, which solidify sulfate-rich Hanford Tank Waste Treatment and Immobilization Plant (WTP) off-gas condensate secondary waste simulant, using deionized water (DIW) 3.conducting the EPA Method 1315 leach tests (EPA 2013) on the grout monoliths made with the new dry blend formulations and three LSW simulants (242-A evaporator condensate, Environmental Restoration Disposal Facility (ERDF) leachate, and WTP off-gas condensate) using two leachants, DIW and simulated Hanford Integrated Disposal Facility (IDF) Site vadose zone pore water (VZPW) 4.estimating the 99Tc desorption Kd (distribution coefficient) values for 99Tc transport in oxidizing conditions to support the IDF performance assessment (PA) 5.estimating the solubility of 99Tc(IV)-bearing solid phases for 99Tc transport in reducing conditions to support the IDF PA.

  19. CHARACTERISATION OF SOLID AND LIQUID PINEAPPLE WASTE

    Directory of Open Access Journals (Sweden)

    Abdullah Abdullah

    2011-07-01

    Full Text Available The pineapple waste is contain high concentration of biodegradable organic material and suspended solid. As a result it has a high BOD and extremes of pH conditions. The pineapple wastes juice contains mainly sucrose, glucose, fructose and other nutrients. The characterisation this waste is needed to reduce it by  recycling to get raw material or  for  conversion into useful product of higher value added products such as organic acid, methane , ethanol, SCP and enzyme. Analysis of sugar indicates that liquid waste contains mainly sucrose, glucose and fructose.  The dominant sugar was fructose, glucose and sucrose.  The fructose and glucose levels were similar to each other, with fructose usually slightly higher than glucose. The total sugar and citric acid content were 73.76 and 2.18 g/l. The sugar content in solid waste is glucose and fructose was 8.24 and 12.17 %, no sucrose on this waste

  20. Conversion of cellulosic wastes to liquid fuels

    Energy Technology Data Exchange (ETDEWEB)

    Kuester, J.L.

    1980-09-01

    The current status and future plans for a project to convert waste cellulosic (biomass) materials to quality liquid hydrocarbon fuels is described. The basic approach is indirect liquefaction, i.e., thermal gasification followed by catalytic liquefaction. The indirect approach results in separation of the oxygen in the biomass feedstock, i.e., oxygenated compounds do not appear in the liquid hydrocarbon fuel product. The process is capable of accepting a wide variety of feedstocks. Potential products include medium quality gas, normal propanol, diesel fuel and/or high octane gasoline. A fluidized bed pyrolysis system is used for gasification. The pyrolyzer can be fluidized with recycle pyrolysis gas, steam or recycle liquefaction system off gas or some combination thereof. Tars are removed in a wet scrubber. Unseparated pyrolysis gases are utilized as feed to a modified Fischer-Tropsch reactor. The liquid condensate from the reactor consists of a normal propanol-water phase and a paraffinic hydrocarbon phase. The reactor can be operated to optimize for either product. The following tasks were specified in the statement of work for the contract period: (1) feedstock studies; (2) gasification system optimization; (3) waste stream characterization; and (4) liquid fuels synthesis. In addition, several equipment improvements were implemented.

  1. Thermoreversible (Ionic-Liquid-Based) Aqueous Biphasic Systems.

    Science.gov (United States)

    Passos, Helena; Luís, Andreia; Coutinho, João A P; Freire, Mara G

    2016-02-04

    The ability to induce reversible phase transitions between homogeneous solutions and biphasic liquid-liquid systems, at pre-defined and suitable operating temperatures, is of crucial relevance in the design of separation processes. Ionic-liquid-based aqueous biphasic systems (IL-based ABS) have demonstrated superior performance as alternative extraction platforms, and their thermoreversible behaviour is here disclosed by the use of protic ILs. The applicability of the temperature-induced phase switching is further demonstrated with the complete extraction of two value-added proteins, achieved in a single-step. It is shown that these temperature-induced mono(bi)phasic systems are significantly more versatile than classical liquid-liquid systems which are constrained by their critical temperatures. IL-based ABS allow to work in a wide range of temperatures and compositions which can be tailored to fit the requirements of a given separation process.

  2. Liquid / liquid biphasic electrochemistry in ultra-turrax dispersed acetonitrile / aqueous electrolyte systems

    Energy Technology Data Exchange (ETDEWEB)

    Watkins, John D. [Department of Chemistry, University of Bath, Claverton Down, Bath, BA2 7AY (United Kingdom); Amemiya, Fumihiro; Atobe, Mahito [Tokyo Institute of Technology, Department of Electronic Chemistry, Yokohama, Kanagawa 2268502 (Japan); Bulman-Page, Philip C. [School of Chemistry, University of East Anglia, Norwich, Norfolk NR4 7TJ (United Kingdom); Marken, Frank, E-mail: F.Marken@bath.ac.u [Department of Chemistry, University of Bath, Claverton Down, Bath, BA2 7AY (United Kingdom)

    2010-12-01

    Unstable acetonitrile | aqueous emulsions generated in situ with ultra-turrax agitation are investigated for applications in dual-phase electrochemistry. Three modes of operation for liquid / liquid aqueous-organic electrochemical processes are demonstrated with no intentionally added electrolyte in the organic phase based on (i) the formation of a water-soluble product in the aqueous phase in the presence of the organic phase, (ii) the formation of a product and ion transfer at the liquid / liquid-electrode triple phase boundary, and (iii) the formation of a water-insoluble product in the aqueous phase which then transfers into the organic phase. A three-electrode electrolysis cell with ultra-turrax agitator is employed and characterised for acetonitrile / aqueous 2 M NaCl two phase electrolyte. Three redox systems are employed in order to quantify the electrolysis cell performance. The one-electron reduction of Ru(NH{sub 3}){sub 6}{sup 3+} in the aqueous phase is employed to determine the rate of mass transport towards the electrode surface and the effect of the presence of the acetonitrile phase. The one-electron oxidation of n-butylferrocene in acetonitrile is employed to study triple phase boundary processes. Finally, the one-electron reduction of cobalticenium cations in the aqueous phase is employed to demonstrate the product transfer from the electrode surface into the organic phase. Potential applications in biphasic electrosynthesis are discussed.

  3. Magnetic Adsorption Method for the Treatment of Metal Contaminated Aqueous Waste

    Energy Technology Data Exchange (ETDEWEB)

    G. B. Cotten (Parsons); J. D. Navratil (INEEL); H. B. Eldredge (U of Idaho)

    1999-03-01

    There have been many recent developments in separation methods used for treating radioactive and non-radioactive metal bearing liquid wastes. These methods have included adsorption, ion exchange, solvent extraction and other chemical and physical techniques. To date very few, if any, of these processes can provide a low cost and environmentally benign solution. Recent research into the use of magnetite for wastewater treatment indicates the potential for magnetite both cost and environment drivers. A brief review of recent work in using magnetite as a sorbent is presented as well as recent work performed in our laboratory using supported magnetite in the presence of an external magnetic field. The application to groundwater and other aqueous waste streams is discussed. Recent research has focused on supporting magnetite in an economical (as compared to the magnetic polymine-epichlorohydrine resin) and inert (non-reactive, chemically or otherwise) environment that promotes both adsorption and satisfactory flow characteristics.

  4. Development of characterization protocol for mixed liquid radioactive waste classification

    Energy Technology Data Exchange (ETDEWEB)

    Zakaria, Norasalwa, E-mail: norasalwa@nuclearmalaysia.gov.my [Waste Technology Development Centre, Malaysian Nuclear Agency, 43000 Kajang, Selangor (Malaysia); Wafa, Syed Asraf [Radioisotop Technology and Innovation, Malaysian Nuclear Agency, 43000 Kajang, Selangor (Malaysia); Wo, Yii Mei [Radiochemistry and Environment, Malaysian Nuclear Agency, 43000 Kajang, Selangor (Malaysia); Mahat, Sarimah [Material Technology Group, Malaysian Nuclear Agency, 43000 Kajang, Selangor (Malaysia)

    2015-04-29

    Mixed liquid organic waste generated from health-care and research activities containing tritium, carbon-14, and other radionuclides posed specific challenges in its management. Often, these wastes become legacy waste in many nuclear facilities and being considered as ‘problematic’ waste. One of the most important recommendations made by IAEA is to perform multistage processes aiming at declassification of the waste. At this moment, approximately 3000 bottles of mixed liquid waste, with estimated volume of 6000 litres are currently stored at the National Radioactive Waste Management Centre, Malaysia and some have been stored for more than 25 years. The aim of this study is to develop a characterization protocol towards reclassification of these wastes. The characterization protocol entails waste identification, waste screening and segregation, and analytical radionuclides profiling using various analytical procedures including gross alpha/ gross beta, gamma spectrometry, and LSC method. The results obtained from the characterization protocol are used to establish criteria for speedy classification of the waste.

  5. Adsorption of phenol and reactive dye from aqueous solution on activated carbons derived from solid wastes.

    Science.gov (United States)

    Nakagawa, Kyuya; Namba, Akio; Mukai, Shin R; Tamon, Hajime; Ariyadejwanich, Pisit; Tanthapanichakoon, Wiwut

    2004-04-01

    Activated carbons were produced from several solid wastes, namely, waste PET, waste tires, refuse derived fuel and wastes generated during lactic acid fermentation from garbage. Activated carbons having various pore size distributions were obtained by the conventional steam-activation method and via the pre-treatment method (i.e., mixture of raw materials with a metal salt, carbonization and acid treatment prior to steam-activation) that was proposed by the authors. The liquid-phase adsorption characteristics of organic compounds from aqueous solution on the activated carbons were determined to confirm the applicability of these carbons, where phenol and a reactive dye, Black5, were employed as representative adsorbates. The hydrophobic surface of the carbons prepared was also confirmed by water vapor adsorption. The characteristics of a typical commercial activated carbon were also measured and compared. It was found that the activated carbons with plentiful mesopores prepared from PET and waste tires had quite high adsorption capacity for large molecules. Therefore they are useful for wastewater treatment, especially, for removal of bulky adsorbates.

  6. The analysis of aqueous mixtures using liquid chromatography-electrospray mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Steven [Iowa State Univ., Ames, IA (United States)

    1999-02-12

    The focus of this dissertation is the use of chromatographic methods coupled with electrospray mass spectrometry (ES-MS) for the determination of both organic and inorganic compounds in aqueous solutions. The combination of liquid chromatography (LC) methods and ES-MS offers one of the foremost methods for determining compounds in complex aqueous solutions. In this work, LC-ES-MS methods are devised using ion exclusion chromatography, reversed phase chromatography, and ion exchange chromatography, as well as capillary electrophoresis (CE). For an aqueous sample, these LC-ES-MS and CE-ES-MS techniques require no sample preparation or analyte derivatization, which makes it possible to observe a wide variety of analytes as they exist in solution. The majority of this work focuses on the use of LC-ES-MS for the determination of unknown products and intermediates formed during electrochemical incineration (ECI), an experimental waste remediation process. This report contains a general introduction to the project and the general conclusions. Four chapters have been removed for separate processing. Titles are: Chapter 2: Determination of small carboxylic acids by ion exclusion chromatography with electrospray mass spectrometry; Chapter 3: Electrochemical incineration of benzoquinone in aqueous media using a quaternary metal oxide electrode in the absence of a soluble supporting electrolyte; Chapter 4: The determination of electrochemical incineration products of 4-chlorophenol by liquid chromatography-electrospray mass spectrometry; and Chapter 5: Determination of small carboxylic acids by capillary electrophoresis with electrospray mass spectrometry.

  7. Modeling Non-aqueous Phase Liquid Displacement Process

    Institute of Scientific and Technical Information of China (English)

    Yang Zhenqing; Shao Changjin; Zhou Guanggang; Qiu Chao

    2007-01-01

    A pore-network model physically based on pore level multiphase flow was used to study the water-non-aqueous phase liquid (NAPL) displacement process, especially the effects of wettability, water-NAPL interfacial tension, the fraction of NAPL-wet pores, and initial water saturation on the displacement. The computed data show that with the wettability of the mineral surfaces changing from strongly water-wet to NAPL-wet, capillary pressure and the NAPL relative permeability gradually decrease, while water-NAPL interfacial tension has little effect on water relative permeability, but initial water saturation has a strong effect on water and NAPL relative permeabilities. The analytical results may help to understand the micro-structure displacement process of non-aqueous phase liquid and to provide the theoretical basis for controlling NAPL migration.

  8. BIOGAS PRODUCTION FROM TOFU LIQUID WASTE ON TREATED AGRICULTURAL WASTES

    Directory of Open Access Journals (Sweden)

    Budy Rahmat

    2014-01-01

    Full Text Available The Tofu Liquid Waste (TLW as a pollution might be processed into biogas which was environmentally friendly and had potential to replace burning wood or oil. However, the waste could not directly be employed as the biogas substrate due to the high nitrogen content which was not suitable to the methanogen microorganism on the biogas digester and did not produce biogas. It was therefore necessary to adapt the carbon-nitrogen ratio in TLW with the addition of other organic materials that had a lower nitrogen content so it would be a suitable substrate for generating biogas. The research was aimed to evaluate the addition of the other organic material on the TLW to increase the biogas production. The results showed that TLW combined with sheep dung, cabbage waste, bamboo leaves and paddy straw respectively produced biogas as much as 14,183, 7,250, 2,400, 895 cm3 in 20 days. The 4 treatments gave the same quality of biogas, which was determined using the water boiling test. The pH fluctuation during the process was in the right pH for anaerobic digestion, thus it was not the limiting factor.

  9. Future radioactive liquid waste streams study

    Energy Technology Data Exchange (ETDEWEB)

    Rey, A.S.

    1993-11-01

    This study provides design planning information for the Radioactive Liquid Waste Treatment Facility (RLWTF). Predictions of estimated quantities of Radioactive Liquid Waste (RLW) and radioactivity levels of RLW to be generated are provided. This information will help assure that the new treatment facility is designed with the capacity to treat generated RLW during the years of operation. The proposed startup date for the RLWTF is estimated to be between 2002 and 2005, and the life span of the facility is estimated to be 40 years. The policies and requirements driving the replacement of the current RLW treatment facility are reviewed. Historical and current status of RLW generation at Los Alamos National Laboratory are provided. Laboratory Managers were interviewed to obtain their insights into future RLW activities at Los Alamos that might affect the amount of RLW generated at the Lab. Interviews, trends, and investigation data are analyzed and used to create scenarios. These scenarios form the basis for the predictions of future RLW generation and the level of RLW treatment capacity which will be needed at LANL.

  10. The reformation of liquid hydrocarbons in an aqueous discharge reactor

    KAUST Repository

    Zhang, Xuming

    2015-04-21

    We present an aqueous discharge reactor for the reformation of liquid hydrocarbons. To increase a dielectric constant of a liquid medium, we added distilled water to iso-octane and n-dodecane. As expected, we found decreased discharge onset voltage and increased discharge power with increased water content. Results using optical emission spectroscopy identified OH radicals and O atoms as the predominant oxidative reactive species with the addition of water. Enriched CH radicals were also visualized, evidencing the existence of cascade carbon-carbon cleavage and dehydrogenation processes in the aqueous discharge. The gaseous product consisted primarily of hydrogen, carbon monoxide, and unsaturated hydrocarbons. The composition of the product was readily adjustable by varying the volume of water added, which demonstrated a significant difference in composition with respect to the tested liquid hydrocarbon. In this study, we found no presence of CO2 emissions or the contamination of the reactor by solid carbon deposition. These findings offer a new approach to the reforming processes of liquid hydrocarbons and provide a novel concept for the design of a practical and compact plasma reformer. © 2015 IOP Publishing Ltd.

  11. Biosorption of arsenic from aqueous solution using dye waste.

    Science.gov (United States)

    Nigam, Shubha; Vankar, Padma S; Gopal, Krishna

    2013-02-01

    The purpose of this study is to examine on removal of arsenic from water by biosorption through potential application of herbal dye wastes. Four different flower dye residues (after extraction of natural dye) viz. Hibiscus rosasinensis, Rosa rosa, Tagetes erecta, and Canna indica were utilized successfully for the removal of arsenic from aqueous solution. Batch studies were carried out for various parameters viz. pH, sorbent dose, contact time, initial metal ion concentration, and temperature. Data were utilized for isothermal, kinetic, and thermodynamic studies. Scanning electron microscopy (SEM), energy-dispersive x-ray spectroscopy (EDAX), and Fourier transform infrared (FTIR) analyses of biomass were performed. The results showed that 1 g/100 ml for 5.0-5.5 h contact time at pH 6.0-7.5 with agitation rate 150 rpm provided 98, 96, 92, and 85 % maximum absorption of arsenic by R. rosa, H. rosasinensis, T. erecta, and C. indica, respectively, at initial concentration of 500 ppb. Data followed Langmuir isotherm showing sorption to be monolayer on heterogeneous surface of biosorbent. Negative values of ΔG° indicated spontaneous nature, whereas ΔH° indicates exothermic nature of system followed by pseudo-first-order adsorption kinetics. FTIR results showed apparent changes in functional group regions after metal chelation. SEM and EDAX analyses showed the changes in surface morphology of all test biosorbents. Herbal dye wastes, used as biosorbent, exhibited significant (85-98 %) removal of arsenic from aqueous solution. Hence, these biosorbents are cost-effective, easily available, eco-friendly, and comparatively more effective than other biosorbents already in use. These may be used to remove arsenic and other toxic metals from water.

  12. 20 CFR 654.406 - Excreta and liquid waste disposal.

    Science.gov (United States)

    2010-04-01

    ... 20 Employees' Benefits 3 2010-04-01 2010-04-01 false Excreta and liquid waste disposal. 654.406 Section 654.406 Employees' Benefits EMPLOYMENT AND TRAINING ADMINISTRATION, DEPARTMENT OF LABOR SPECIAL RESPONSIBILITIES OF THE EMPLOYMENT SERVICE SYSTEM Housing for Agricultural Workers Housing Standards § 654.406 Excreta and liquid waste disposal....

  13. Internal Mainland Nuclear Power Liquid Waste Treatment Technology

    Institute of Scientific and Technical Information of China (English)

    YOU; Xin-feng; ZHANG; Zhen-tao; ZHENG; Wen-jun; WANG; Lei; YANG; Lin-yue; HUA; Xiao-hui; ZHENG; Yu; YANG; Yong-gang; WU; Yan

    2013-01-01

    Taohuajiang power station is the first internal mainland nuclear power station,and it adopts AP1000nuclear technology belongs to the Westinghouse Electric Corporation.To ensure the safety of the environment around the station and satisfy the radio liquid waste discharge standards,our team has researched the liquid waste treatment technology for the internal mainland nuclear power plant.According

  14. Olefin Epoxidation in Aqueous Phase Using Ionic-Liquid Catalysts.

    Science.gov (United States)

    Cokoja, Mirza; Reich, Robert M; Wilhelm, Michael E; Kaposi, Marlene; Schäffer, Johannes; Morris, Danny S; Münchmeyer, Christian J; Anthofer, Michael H; Markovits, Iulius I E; Kühn, Fritz E; Herrmann, Wolfgang A; Jess, Andreas; Love, Jason B

    2016-07-21

    Hydrophobic imidazolium-based ionic liquids (IL) act as catalysts for the epoxidation of unfunctionalized olefins in water using hydrogen peroxide as oxidant. Although the catalysts are insoluble in both the substrate and in water, surprisingly, they are very well soluble in aqueous H2 O2 solution, owing to perrhenate-H2 O2 interactions. Even more remarkably, the presence of the catalyst also boosts the solubility of substrate in water. This effect is crucially dependent on the cation design. Hence, the imidazolium perrhenates enable both the transfer of hydrophobic substrate into the aqueous phase, and serve as actual catalysts, which is unprecedented. At the end of the reaction and in absence of H2 O2 the IL catalyst forms a third phase next to the lipophilic product and water and can easily be recycled.

  15. Low-liquid pretreatment of corn stover with aqueous ammonia.

    Science.gov (United States)

    Li, Xuan; Kim, Tae Hyun

    2011-04-01

    A low-liquid pretreatment method of corn stover using aqueous ammonia was studied to reduce the severity and liquid throughput associated with the pretreatment step for ethanol production. Corn stover was treated at 0.5-50.0 wt.% of ammonia loading, 1:0.2-5.0 (w/w) of solid-to-liquid ratio, 30 °C for 4-12 weeks. The effects of these conditions on the composition and enzyme digestibility of pretreated corn stover were investigated. Pretreatment of corn stover at 30°C for four weeks using 50 wt.% of ammonia loading and 1:5 solid-to-liquid ratio resulted in 55% delignification and 86.5% glucan digestibility with 15 FPU cellulase+30 CBU β-glucosidase/g-glucan. Simultaneous saccharification and fermentation of corn stover treated at 30 °C for four weeks using 50 wt.% ammonia loading and 1:2 solid-to-liquid ratio gave an ethanol yield of 73% of the theoretical maximum based on total carbohydrates (glucan+xylan) present in the untreated material.

  16. Fluidized bed combustion of pesticide-manufacture liquid wastes

    Directory of Open Access Journals (Sweden)

    SAŠA MILETIĆ

    2010-04-01

    Full Text Available Industrial liquid wastes can be in the form of solutions, suspensions, sludges, scums or waste oil and have organic properties. The objective of this work was to demonstrate the technical feasibility of a fluidized bed as a clean technology for burning liquid waste from a pesticide production plant. The combustion of liquid waste mixtures, obtained from realistic samples, was investigated in a pilot scale fluidized bed with quartz sand particles of 0.63–1.25 mm in diameter and 2610 kg/m3 in density at 800–950 °C. To ensure complete combustion of liquid waste and additional fuel, the combustion chamber was supplied with excess air and the U/UmF (at ambient temperature was in between 1.1 and 2.3. In the fluidized bed chamber, liquid waste, additional liquid fuel and air can be brought into intense contact sufficient to permit combustion in bed without backfire problems. The experimental results show that the fluidized bed furnace offers excellent thermal uniformity and temperature control. The results of the combustion tests showed that degradation of liquid wastes can be successfully realized in a fluidized bed with no harmful gaseous emissions by ensuring that the temperatures of both the bed and the freeboard are not lower than 900 °C.

  17. Evaluation of mercury in the liquid waste processing facilities

    Energy Technology Data Exchange (ETDEWEB)

    Jain, Vijay [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Shah, Hasmukh [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Occhipinti, John E. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Wilmarth, William R. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Edwards, Richard E. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2015-08-13

    This report provides a summary of Phase I activities conducted to support an Integrated Evaluation of Mercury in Liquid Waste System (LWS) Processing Facilities. Phase I activities included a review and assessment of the liquid waste inventory and chemical processing behavior of mercury using a system by system review methodology approach. Gaps in understanding mercury behavior as well as action items from the structured reviews are being tracked. 64% of the gaps and actions have been resolved.

  18. Membrane Treatment of Liquid Salt Bearing Radioactive Wastes

    Energy Technology Data Exchange (ETDEWEB)

    Dmitriev, S. A.; Adamovich, D. V.; Demkin, V. I.; Timofeev, E. M.

    2003-02-25

    The main fields of introduction and application of membrane methods for preliminary treatment and processing salt liquid radioactive waste (SLRW) can be nuclear power stations (NPP) and enterprises on atomic submarines (AS) utilization. Unlike the earlier developed technology for the liquid salt bearing radioactive waste decontamination and concentrating this report presents the new enhanced membrane technology for the liquid salt bearing radioactive waste processing based on the state-of-the-art membrane unit design, namely, the filtering units equipped with the metal-ceramic membranes of ''TruMem'' brand, as well as the electrodialysis and electroosmosis concentrators. Application of the above mentioned units in conjunction with the pulse pole changer will allow the marked increase of the radioactive waste concentrating factor and the significant reduction of the waste volume intended for conversion into monolith and disposal. Besides, the application of the electrodialysis units loaded with an ion exchange material at the end polishing stage of the radioactive waste decontamination process will allow the reagent-free radioactive waste treatment that meets the standards set for the release of the decontaminated liquid radioactive waste effluents into the natural reservoirs of fish-farming value.

  19. Fast Tritium Separation From the Low Level Radioactive Liquid Waste

    Institute of Scientific and Technical Information of China (English)

    LIANG; Xiao-hu; YANG; Su-liang; YANG; Lei; YANG; Jin-ling

    2012-01-01

    <正>Due to the needed of high efficiency monitoring and controlling of the waste water generated from the spent fuel reprocessing process, analyzing work need to be done quickly. Tritium is an important nuclide in the liquid waste and its content must be determined. But the existing tritium analysis method

  20. Aqueous biphasic systems involving alkylsulfate-based ionic liquids

    Energy Technology Data Exchange (ETDEWEB)

    Deive, Francisco J. [Instituto de Tecnologia Quimica e Biologica, UNL, Av. Republica, Apartado 127, 2780-901 Oeiras (Portugal); Department of Chemical Engineering, University of Vigo, P.O. Box 36310, Vigo (Spain); Rodriguez, Ana [Department of Chemical Engineering, University of Vigo, P.O. Box 36310, Vigo (Spain); Marrucho, Isabel M., E-mail: imarrucho@itqb.unl.pt [Instituto de Tecnologia Quimica e Biologica, UNL, Av. Republica, Apartado 127, 2780-901 Oeiras (Portugal); Rebelo, Luis P.N. [Instituto de Tecnologia Quimica e Biologica, UNL, Av. Republica, Apartado 127, 2780-901 Oeiras (Portugal)

    2011-11-15

    Highlights: > K{sub 3}PO{sub 4}, K{sub 2}CO{sub 3}, Na{sub 2}CO{sub 3}, and (NH{sub 4}){sub 2}SO{sub 4} act as phase promoter in aqueous solutions of ILs. > Remarkable influence of alkyl-chain length on solubility curves of alkylsulfate-based ILs. > Merchuck correlation was used for describing these systems. > {Delta}S{sub hyd} and Hofmeister series were used to discuss the different salting out effects. - Abstract: The specific effects of K{sub 3}PO{sub 4}, K{sub 2}CO{sub 3}, Na{sub 2}CO{sub 3}, and (NH{sub 4}){sub 2}SO{sub 4}, as high charge-density inorganic salts and thus inducers of the formation of aqueous biphasic systems (ABS) containing several ethyl-methylimidazolium alkylsulfate ionic liquids, C{sub 2}MIM C{sub n}SO{sub 4} (n = 2, 4, 6, or 8), have been assessed at T = 298.15 K. The results are analyzed in the light of the Hofmeister series. The influence of different alkyl chain lengths in the anion, together with the ability of the selected inorganic salts to induce the formation of ABS, is discussed. Phase diagrams have been determined through turbidimetry, including tie lines assignments from mass phase ratios according to the lever - arm rule. The Merchuck equation was satisfactorily used to correlate the solubility curve.

  1. Radioactive Liquid Waste Treatment Facility: Environmental Information Document

    Energy Technology Data Exchange (ETDEWEB)

    Haagenstad, H.T.; Gonzales, G.; Suazo, I.L. [Los Alamos National Lab., NM (United States)

    1993-11-01

    At Los Alamos National Laboratory (LANL), the treatment of radioactive liquid waste is an integral function of the LANL mission: to assure U.S. military deterrence capability through nuclear weapons technology. As part of this mission, LANL conducts nuclear materials research and development (R&D) activities. These activities generate radioactive liquid waste that must be handled in a manner to ensure protection of workers, the public, and the environment. Radioactive liquid waste currently generated at LANL is treated at the Radioactive Liquid Waste Treatment Facility (RLWTF), located at Technical Area (TA)-50. The RLWTF is 30 years old and nearing the end of its useful design life. The facility was designed at a time when environmental requirements, as well as more effective treatment technologies, were not inherent in engineering design criteria. The evolution of engineering design criteria has resulted in the older technology becoming less effective in treating radioactive liquid wastestreams in accordance with current National Pollutant Discharge Elimination System (NPDES) and Department of Energy (DOE) regulatory requirements. Therefore, to support ongoing R&D programs pertinent to its mission, LANL is in need of capabilities to efficiently treat radioactive liquid waste onsite or to transport the waste off site for treatment and/or disposal. The purpose of the EID is to provide the technical baseline information for subsequent preparation of an Environmental Impact Statement (EIS) for the RLWTF. This EID addresses the proposed action and alternatives for meeting the purpose and need for agency action.

  2. Valorization of Waste Lipids through Hydrothermal Catalytic Conversion to Liquid Hydrocarbon Fuels with in Situ Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Dongwook; Vardon, Derek R.; Murali, Dheeptha; Sharma, Brajendra K.; Strathmann, Timothy J.

    2016-03-07

    We demonstrate hydrothermal (300 degrees C, 10 MPa) catalytic conversion of real waste lipids (e.g., waste vegetable oil, sewer trap grease) to liquid hydrocarbon fuels without net need for external chemical inputs (e.g., H2 gas, methanol). A supported bimetallic catalyst (Pt-Re/C; 5 wt % of each metal) previously shown to catalyze both aqueous phase reforming of glycerol (a triacylglyceride lipid hydrolysis coproduct) to H2 gas and conversion of oleic and stearic acid, model unsaturated and saturated fatty acids, to linear alkanes was applied to process real waste lipid feedstocks in water. For reactions conducted with an initially inert headspace gas (N2), waste vegetable oil (WVO) was fully converted into linear hydrocarbons (C15-C17) and other hydrolyzed byproducts within 4.5 h, and H2 gas production was observed. Addition of H2 to the initial reactor headspace accelerated conversion, but net H2 production was still observed, in agreement with results obtained for aqueous mixtures containing model fatty acids and glycerol. Conversion to liquid hydrocarbons with net H2 production was also observed for a range of other waste lipid feedstocks (animal fat residuals, sewer trap grease, dry distiller's grain oil, coffee oil residual). These findings demonstrate potential for valorization of waste lipids through conversion to hydrocarbons that are more compatible with current petroleum-based liquid fuels than the biodiesel and biogas products of conventional waste lipid processing technologies.

  3. Biosorption of uranium in radioactive liquid organic waste by coconut fiber

    Energy Technology Data Exchange (ETDEWEB)

    Marumo, Julio Takehiro; Ferreira, Eduardo Gurzoni Alvares; Vieira, Ludmila Cabreira; Ferreira, Rafael Vicente de Padua, E-mail: jtmarumo@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Silva, Edson Antonio da, E-mail: edson.silva2@unioeste.br [Universidade Estadual do Oeste do Parana (UNIOESTE), Toledo, PR (Brazil)

    2013-07-01

    Radioactive liquid organic waste needs special attention because the available treatment processes are often expensive and difficult to be managed. Biosorption is a potential technique since it allies low cost with relatively high efficiency. Biosorption has been defined as the property of certain biomolecules to bind and remove selected ions or other molecules from aqueous solutions. Biosorption using vegetable biomass from agricultural waste has become a very attractive technique because it involves the removal of heavy metal ions by low cost biosorbent. This technique could be employed in the treatment of radioactive liquid wastes. Among the biosorbent reported in the literature, coconut fiber (Cocos nucifera L.) is highlighted due to the large number of functional groups in its composition. The aim of this study was to assess the potential of coconut fiber to remove uranium from radioactive liquid organic waste. This work was divided into three stages: 1) Preparation and activation of the coconut fiber; 2) Physical characterization of the biomass, 3) Batch biosorption experiments. Two forms of coconut fiber were tested, raw and activated. The activation was performed with dilute HNO3 and NaOH solutions. The parameters evaluated for physical characterization of biomass were morphological characteristics of coconut fiber, real and apparent density and surface area. The biomass was suspended in 10 ml of solutions prepared with distillate water and radioactive liquid waste for 2 hours in the proportion of 0.2% w/v. After the contact time, the coconut fiber was removed by filtration and the supernatant, analyzed by inductively coupled plasma optical emission spectrometry (ICP-OES).The results were evaluated using Langmuir and Freundlich isotherms. The maximum capacity for the raw coconut fiber was lower than the activated one, removing only 1.14mg/g against 2.61mg/g. These results suggest that biosorption with coconut fiber in activated form can be applied in the

  4. Behavior of supercooled aqueous solutions stemming from hidden liquid-liquid transition in water

    Science.gov (United States)

    Biddle, John W.; Holten, Vincent; Anisimov, Mikhail A.

    2014-08-01

    A popular hypothesis that explains the anomalies of supercooled water is the existence of a metastable liquid-liquid transition hidden below the line of homogeneous nucleation. If this transition exists and if it is terminated by a critical point, the addition of a solute should generate a line of liquid-liquid critical points emanating from the critical point of pure metastable water. We have analyzed thermodynamic consequences of this scenario. In particular, we consider the behavior of two systems, H2O-NaCl and H2O-glycerol. We find the behavior of the heat capacity in supercooled aqueous solutions of NaCl, as reported by Archer and Carter [J. Phys. Chem. B 104, 8563 (2000)], to be consistent with the presence of the metastable liquid-liquid transition. We elucidate the non-conserved nature of the order parameter (extent of "reaction" between two alternative structures of water) and the consequences of its coupling with conserved properties (density and concentration). We also show how the shape of the critical line in a solution controls the difference in concentration of the coexisting liquid phases.

  5. Corrosion experience in calcination of liquid nuclear waste

    Energy Technology Data Exchange (ETDEWEB)

    Zimmerman, C A

    1980-01-01

    The Waste Calcining Facility (WCF) at the Idaho National Engineering Laboratory became operational in 1963. Since that time, approximately 13,337,137 litres (3,523,375 gallons) of liquid nuclear wastes, generated during the reprocessing of spent nuclear fuel materials, have been reduced to dry granular solids. The volume reduction is about seven or eight gallons of liquid waste to one gallon of dry granular solids. This paper covers some of the corrosion experiences encountered in over fifteen years of operating that calcination facility. 7 figures, 7 tables.

  6. Non-aqueous phase liquid spreading during soil vapor extraction

    Science.gov (United States)

    Kneafsey, Timothy J.; Hunt, James R.

    2004-02-01

    Many non-aqueous phase liquids (NAPLs) are expected to spread at the air-water interface, particularly under non-equilibrium conditions. In the vadose zone, this spreading should increase the surface area for mass transfer and the efficiency of volatile NAPL recovery by soil vapor extraction (SVE). Observations of spreading on water wet surfaces led to a conceptual model of oil spreading vertically above a NAPL pool in the vadose zone. Analysis of this model predicts that spreading can enhance the SVE contaminant recovery compared to conditions where the liquid does not spread. Experiments were conducted with spreading volatile oils hexane and heptane in wet porous media and capillary tubes, where spreading was observed at the scale of centimeters. Within porous medium columns up to a meter in height containing stagnant gas, spreading was less than ten centimeters and did not contribute significantly to hexane volatilization. Water film thinning and oil film pinning may have prevented significant oil film spreading, and thus did not enhance SVE at the scale of a meter. The experiments performed indicate that volatile oil spreading at the field scale is unlikely to contribute significantly to the efficiency of SVE.

  7. APPLICATION OF PULSE COMBUSTION TO INCINERATION OF LIQUID HAZARDOUS WASTE

    Science.gov (United States)

    The report gives results of a study to determine the effect of acoustic pulsations on the steady-state operation of a pulse combustor burning liquid hazardous waste. A horizontal tunnel furnace was retrofitted with a liquid injection pulse combustor that burned No. 2 fuel oil. Th...

  8. Sorption Potentials of Waste Tyre for Some Heavy Metals (Pb Cd in Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Austin Kanayo ASIAGWU

    2009-07-01

    Full Text Available An investigation into the adsorption potential of activated and inactivated waste tyre powders for some heavy metals (Pb2+ and Cd2+ in their aqueous solution has been studied. The result indicated that inactivated waste tyre is a good non-conventional adsorbent for the removal of Cd from aqueous solution. A total of 93.3% of Cadmium contents was removed. The inactivated waste type proved a good adsorbent for the removal of Pb2+ 5g of 500mm activated tyre removed over 86.66% of Pb2+ from solution.

  9. ICPP radioactive liquid and calcine waste technologies evaluation. Interim report

    Energy Technology Data Exchange (ETDEWEB)

    Murphy, J.A.; Pincock, L.F.; Christiansen, I.N.

    1994-06-01

    The Department of Energy (DOE) has received spent nuclear fuel (SNF) at the Idaho Chemical Processing Plant (ICPP) for interim storage since 1951 and reprocessing since 1953. Until recently, the major activity of the ICPP has been the reprocessing of SNF to recover fissile uranium; however, changing world events have raised questions concerning the need to recover and recycle this material. In April 1992, DOE chose to discontinue reprocessing SNF for uranium recovery and shifted its focus toward the management and disposition of radioactive wastes accumulated through reprocessing activities. Currently, 1.8 million gallons of radioactive liquid wastes (1.5 million gallons of radioactive sodium-bearing liquid wastes and 0.3 million gallons of high-level liquid waste) and 3,800 cubic meters (m{sup 3}) of calcine waste are in inventory at the ICPP. Legal drivers and agreements exist obligating the INEL to develop, demonstrate, and implement technologies for safe and environmentally sound treatment and interim storage of radioactive liquid and calcine waste. Candidate treatment processes and waste forms are being evaluated using the Technology Evaluation and Analysis Methodology (TEAM) Model. This process allows decision makers to (1) identify optimum radioactive waste treatment and disposal form alternatives; (2) assess tradeoffs between various optimization criteria; (3) identify uncertainties in performance parameters; and (4) focus development efforts on options that best satisfy stakeholder concerns. The Systems Analysis technology evaluation presented in this document supports the DOE in selecting the most effective radioactive liquid and calcine waste management plan to implement in compliance with established regulations, court orders, and agreements.

  10. Dynamic Mass Transfer of Hemoglobin at the Aqueous/Ionic-Liquid Interface Monitored with Liquid Core Optical Waveguide.

    Science.gov (United States)

    Chen, Xuwei; Yang, Xu; Zeng, Wanying; Wang, Jianhua

    2015-08-04

    Protein transfer from aqueous medium into ionic liquid is an important approach for the isolation of proteins of interest from complex biological samples. We hereby report a solid-cladding/liquid-core/liquid-cladding sandwich optical waveguide system for the purpose of monitoring the dynamic mass-transfer behaviors of hemoglobin (Hb) at the aqueous/ionic liquid interface. The optical waveguide system is fabricated by using a hydrophobic IL (1,3-dibutylimidazolium hexafluorophosphate, BBimPF6) as the core, and protein solution as one of the cladding layer. UV-vis spectra are recorded with a CCD spectrophotometer via optical fibers. The recorded spectra suggest that the mass transfer of Hb molecules between the aqueous and ionic liquid media involve accumulation of Hb on the aqueous/IL interface followed by dynamic extraction/transfer of Hb into the ionic liquid phase. A part of Hb molecules remain at the interface even after the accomplishment of the extraction/transfer process. Further investigations indicate that the mass transfer of Hb from aqueous medium into the ionic liquid phase is mainly driven by the coordination interaction between heme group of Hb and the cationic moiety of ionic liquid, for example, imidazolium cation in this particular case. In addition, hydrophobic interactions also contribute to the transfer of Hb.

  11. Extraction of proteins with ionic liquid aqueous two-phase system based on guanidine ionic liquid.

    Science.gov (United States)

    Zeng, Qun; Wang, Yuzhi; Li, Na; Huang, Xiu; Ding, Xueqin; Lin, Xiao; Huang, Songyun; Liu, Xiaojie

    2013-11-15

    Eight kinds of green ionic liquids were synthesized, and an ionic liquid aqueous two-phase system (ILATPS) based on 1,1,3,3-tetramethylguandine acrylate (TMGA) guanidine ionic liquid was first time studied for the extraction of proteins. Single factor experiments proved that the extraction efficiency of bovine serum albumin (BSA) was influenced by the mass of IL, K2HPO4 and BSA, also related to the separation time and temperature. The optimum conditions were determined through orthogonal experiment by the five factors described above. The results showed that under the optimum conditions, the extraction efficiency could reach up to 99.6243%. The relative standard deviations (RSD) of extraction efficiencies in precision experiment, repeatability experiment and stability experiment were 0.8156% (n=5), 1.6173% (n=5) and 1.6292% (n=5), respectively. UV-vis and FT-IR spectra confirmed that there were no chemical interactions between BSA and ionic liquid in the extraction process, and the conformation of the protein was not changed after extraction. The conductivity, DLS and TEM were combined to investigate the microstructure of the top phase and the possible mechanism for the extraction. The results showed that hydrophobic interaction, hydrogen bonding interaction and the salt out effect played important roles in the transferring process, and the aggregation and embrace phenomenon was the main driving force for the separation. All these results proved that guanidine ionic liquid-based ATPSs have the potential to offer new possibility in the extraction of proteins.

  12. Measurement and Monte Carlo Calculation of Waste Drum Filled With Radioactive Aqueous Solution

    Institute of Scientific and Technical Information of China (English)

    XU; Li-jun; ZHANG; Wei-dong; YE; Hong-sheng; LIN; Min; CHEN; Xi-lin; GUO; Xiao-qing

    2012-01-01

    <正>Theoretically the best calibrating source of gamma scan system (SGS) is a waste drum filled with uniform distribution of medium and radioactive nuclides. However, in reality, waste drums usually full of solid substance, which are difficult to be prepared in a completely uniformly distributed state. To reduce measurement uncertainty of the radioactivity of waste drums prepared using the method of shell source, a waste drum filled with radioactive aqueous solution was prepared. Besides, its radioactivity was measured by a SGS device and calculated using Monte Carlo method to verify the exact geometric model, which

  13. Single Molecule Electrochemical Detection in Aqueous Solutions and Ionic Liquids.

    Science.gov (United States)

    Byers, Joshua C; Paulose Nadappuram, Binoy; Perry, David; McKelvey, Kim; Colburn, Alex W; Unwin, Patrick R

    2015-10-20

    Single molecule electrochemical detection (SMED) is an extremely challenging aspect of electroanalytical chemistry, requiring unconventional electrochemical cells and measurements. Here, SMED is reported using a "quad-probe" (four-channel probe) pipet cell, fabricated by depositing carbon pyrolytically into two diagonally opposite barrels of a laser-pulled quartz quadruple-barreled pipet and filling the open channels with electrolyte solution, and quasi-reference counter electrodes. A meniscus forms at the end of the probe covering the two working electrodes and is brought into contact with a substrate working electrode surface. In this way, a nanogap cell is produced whereby the two carbon electrodes in the pipet can be used to promote redox cycling of an individual molecule with the substrate. Anticorrelated currents generated at the substrate and tip electrodes, at particular distances (typically tens of nanometers), are consistent with the detection of single molecules. The low background noise realized in this droplet format opens up new opportunities in single molecule electrochemistry, including the use of ionic liquids, as well as aqueous solution, and the quantitative assessment and analysis of factors influencing redox cycling currents, due to a precisely known gap size.

  14. Straining soft colloids in aqueous nematic liquid crystals

    Science.gov (United States)

    Mushenheim, Peter C.; Pendery, Joel S.; Weibel, Douglas B.; Spagnolie, Saverio E.; Abbott, Nicholas L.

    2016-05-01

    Liquid crystals (LCs), because of their long-range molecular ordering, are anisotropic, elastic fluids. Herein, we report that elastic stresses imparted by nematic LCs can dynamically shape soft colloids and tune their physical properties. Specifically, we use giant unilamellar vesicles (GUVs) as soft colloids and explore the interplay of mechanical strain when the GUVs are confined within aqueous chromonic LC phases. Accompanying thermal quenching from isotropic to LC phases, we observe the elasticity of the LC phases to transform initially spherical GUVs (diameters of 2-50 µm) into two distinct populations of GUVs with spindle-like shapes and aspect ratios as large as 10. Large GUVs are strained to a small extent (R/r minor radii, respectively), consistent with an LC elasticity-induced expansion of lipid membrane surface area of up to 3% and conservation of the internal GUV volume. Small GUVs, in contrast, form highly elongated spindles (1.54 materials and suggest previously unidentified designs of LC-based responsive and reconfigurable materials.

  15. Removal of phenols from aqueous solutions by emulsion liquid membranes.

    Science.gov (United States)

    Reis, M Teresa A; Freitas, Ondina M F; Agarwal, Shiva; Ferreira, Licínio M; Ismael, M Rosinda C; Machado, Remígio; Carvalho, Jorge M R

    2011-09-15

    The present study deals with the extraction of phenols from aqueous solutions by using the emulsion liquid membranes technique. Besides phenol, two derivatives of phenol, i.e., tyrosol (2-(4-hydroxyphenyl)ethanol) and p-coumaric acid (4-hydroxycinnamic acid), which are typical components of the effluents produced in olive oil plants, were selected as the target solutes. The effect of the composition of the organic phase on the removal of solutes was examined. The influence of pH of feed phase on the extraction of tyrosol and p-coumaric was tested for the membrane with Cyanex 923 as an extractant. The use of 2% Cyanex 923 allowed obtaining a very high extraction of phenols (97-99%) in 5-6 min of contact time for either single solute solutions or for their mixtures. The removal efficiency of phenol and p-coumaric acid attained equivalent values by using the system with 2% isodecanol, but the removal rate of tyrosol was found greatly reduced. The extraction of tyrosol and p-coumaric acid from their binary mixture was also analysed for different operating conditions like the volume ratio of feed phase to stripping phase (sodium hydroxide), the temperature and the initial concentration of solute in the feed phase.

  16. Radioactive liquid waste treatment for decontamination and decommissioning of TRIGA research reactors

    Energy Technology Data Exchange (ETDEWEB)

    Park, Seung Kook; Chung, K.H

    1999-04-01

    All of operated radioactive liquid waste will be stored by using existing collection tank and temporally transfer piping system before dismantle the TRIGA research reactors. In this paper, there are presented and discussed as follows; 1.The status of operated radioactive liquid waste. 2. The radioactive liquid waste during dismantle the reactor. 3. Radiological status of radioactive liquid waste. 4. The classification criteria and method radioactive liquid waste. 6. The collection and transportation of radioactive liquid waste. (Author). 13 refs., 13 tabs., 8 figs.

  17. Liquid and Gaseous Waste Operations Department Annual Operating Report, CY 1993

    Energy Technology Data Exchange (ETDEWEB)

    Maddox, J.J.; Scott, C.B.

    1994-02-01

    This report summarizes the activities of the waste management operations section of the liquid and gaseous waste operations department at ORNL for 1993. The process waste, liquid low-level waste, gaseous waste systems activities are reported, as well as the low-level waste solidification project. Upgrade activities is the various waste processing and treatment systems are summarized. A maintenance activity overview is provided, and program management, training, and other miscellaneous activities are covered.

  18. Technical report on treatment of radioactive slurry liquid waste

    Energy Technology Data Exchange (ETDEWEB)

    Jeong, Gyeong Hwan; Jo, Eun Sung; Park, Seung Kook; Jung, Ki Jung

    1999-06-01

    By literature survey, this report deals with the technology on typical pre-treatment and filtration of radioactive slurry liquid waste, produced during the operation of TRIGA Mark-II, III research reactor, and produced during the decommission/decontamination of TRIGA Mark-II, III research reactor. It is reviewed pre-treatment procedure, both physical and chemical that optimise the dewatering characteristics, and also surveyed types of dewatering devices based on centrifuges, vacuum and pressure filters with particular reference to various combined field approaches using two or more complementary driving forces to achieve better performance. Dewatering operations and devises on filtration of radioactive slurry liquid waste are also analysed. (author)

  19. Transfer Kinetics at the Aqueous/Non-Aqueous Phase Liquid Interface. A Statistical Mechanic Approach

    Science.gov (United States)

    Doss, S. K.; Ezzedine, S.; Ezzedine, S.; Ziagos, J. P.; Hoffman, F.; Gelinas, R. J.

    2001-05-01

    Many modeling efforts in the literature use a first-order, linear-driving-force model to represent the chemical dissolution process at the non-aqueous/aqueous phase liquid (NAPL/APL) interface. In other words, NAPL to APL phase flux is assumed to be equal to the difference between the solubility limit and the "bulk aqueous solution" concentrations times a mass transfer coefficient. Under such assumptions, a few questions are raised: where, in relation to a region of pure NAPL, does the "bulk aqueous solution" regime begin and how does it behave? The answers are assumed to be associated with an arbitrary, predetermined boundary layer, which separates the NAPL from the surrounding solution. The mass transfer rate is considered to be, primarily, limited by diffusion of the component through the boundary layer. In fact, compositional models of interphase mass transfer usually assume that a local equilibrium is reached between phases. Representing mass flux as a rate-limiting process is equivalent to assuming diffusion through a stationary boundary layer with an instantaneous local equilibrium and linear concentration profile. Some environmental researchers have enjoyed success explaining their data using chemical engineering-based correlations. Correlations are strongly dependent on the experimental conditions employed. A universally applicable theory for NAPL dissolution in natural systems does not exist. These correlations are usually expressed in terms of the modified Sherwood number as a function of Reynolds, Peclet, and Schmidt numbers. The Sherwood number may be interpreted as the ratio between the grain size and the thickness of the Nernst stagnant film. In the present study, we show that transfer kinetics at the NAPL/APL interface under equilibrium conditions disagree with approaches based on the Nernst stagnant film concept. It is unclear whether local equilibrium assumptions used in current models are suitable for all situations.A statistical mechanic

  20. Primitive Liquid Water of the Solar System in an Aqueous Altered Carbonaceous Chondrite

    Science.gov (United States)

    Tsuchiyama, A.; Miyake, A.; Kitayama, A.; Matsuno, J.; Takeuchi, A.; Uesugi, K.; Suzuki, Y.; Nakano, T.; Zolensky, M. E.

    2016-01-01

    Non-destructive 3D observations of the aqueous altered CM chondrite Sutter's Mill using scanning imaging x-ray microscopy (SIXM) showed that some of calcite and enstatite grains contain two-phase inclusion, which is most probably composed of liquid water and bubbles. This water should be primitive water responsible for aqueous alteration in an asteroid in the early solar system.

  1. Modelling aqueous corrosion of nuclear waste phosphate glass

    Science.gov (United States)

    Poluektov, Pavel P.; Schmidt, Olga V.; Kascheev, Vladimir A.; Ojovan, Michael I.

    2017-02-01

    A model is presented on nuclear sodium alumina phosphate (NAP) glass aqueous corrosion accounting for dissolution of radioactive glass and formation of corrosion products surface layer on the glass contacting ground water of a disposal environment. Modelling is used to process available experimental data demonstrating the generic inhibiting role of corrosion products on the NAP glass surface.

  2. Solid waste removes toxic liquid waste: adsorption of chromium(VI) by iron complexed protein waste.

    Science.gov (United States)

    Fathima, Nishtar Nishad; Aravindhan, Rathinam; Rao, Jonnalagadda Raghava; Nair, Balachandran Unni

    2005-04-15

    The leather processing industry generates huge amounts of wastes, both in solid and liquid form. Fleshing from animal hides/skins is one such waste that is high in protein content. In this study, raw fleshing has been complexed with iron and is used for removal of chromium(VI). The effect of pH and the initial concentration of chromium(VI) on the removal of Cr(IV) by iron treated fleshing is presented. Iron treatment is shown to greatly improve adsorption of the fleshing for hexavalent chromium. The ultimate adsorption capacity of iron treated fleshing is 51 mg of chromium(VI) per gram of fleshing. That of untreated fleshing is 9 mg/g such that iron treatment increases the adsorption capacity of fleshing by 10-fold. The measured adsorption kinetics is well described by a pseudo-second-order kinetic model. The uptake of chromium(VI) by fleshing is best described by the Langmuir adsorption isotherm model. X-ray photoelectron spectroscopic (XPS) studies show that the iron is incorporated into the protein matrix. Shifts in XPS spectra suggest that dichromate binding occurs with iron at active adsorption sites and that iron treated fleshing removes chromium(VI) without reducing it to chromium(III).

  3. Secondary and lyotropic liquid crystal membranes for improved aqueous separations

    Science.gov (United States)

    Nemade, Parag Ramesh

    An effective membrane separation process should have high flux (i.e., volume filtered per unit membrane surface area per unit time) and selectivity (i.e., passage of the desired species and rejection of undesired species). This dissertation examined two approaches, secondary membranes and lyotropic liquid crystal membranes, for improving flux and selectivity in aqueous liquid separations. The first part of my work emphasizes the use of pre-deposited secondary membranes and backflushing for controlling membrane fouling in microfiltration and ultrafiltration of biological mixtures. Use of secondary membranes increased the permeate flux in microfiltration by several fold. Protein transmission is also enhanced due to the presence of the secondary membrane, and the amount of protein recovered is more than twice that obtained during filtration of protein-only solutions under otherwise identical conditions. In ultrafiltration, the flux enhancement due to secondary membranes is 50%, or less. For the second part of my research, I developed and evaluated polymerized lyotropic liquid crystal (LLC) thin-film composite membranes. LLC assemblies provide an opportunity to make nanoporous polymer membranes with precise control over chemical and structural features on the nanometer scale, which is currently lacking in commercial reverse osmosis (RO) and nanofiltration (NF) membranes available today. These LLC composite membranes are prepared by photopolymerization of solution-cast films of LLC monomer on an ultrafiltration support membrane. These LLC membranes appeared to exhibit almost linearly increasing ionic rejection based on ionic diameter. LLC monomer was modified to achieve a 15% reduction in channel diameter, through the use of a larger multivalent Eu3+ cation as the carboxylate counterion. However, the monomers synthesized required use of solvents such as tetrahydrofuran, which resulted in the dissolution and damage of the support membranes used. Therefore, this direction

  4. Iraq liquid radioactive waste tanks maintenance and monitoring program plan.

    Energy Technology Data Exchange (ETDEWEB)

    Dennis, Matthew L.; Cochran, John Russell; Sol Shamsaldin, Emad (Iraq Ministry of Science and Technology)

    2011-10-01

    The purpose of this report is to develop a project management plan for maintaining and monitoring liquid radioactive waste tanks at Iraq's Al-Tuwaitha Nuclear Research Center. Based on information from several sources, the Al-Tuwaitha site has approximately 30 waste tanks that contain varying amounts of liquid or sludge radioactive waste. All of the tanks have been non-operational for over 20 years and most have limited characterization. The program plan embodied in this document provides guidance on conducting radiological surveys, posting radiation control areas and controlling access, performing tank hazard assessments to remove debris and gain access, and conducting routine tank inspections. This program plan provides general advice on how to sample and characterize tank contents, and how to prioritize tanks for soil sampling and borehole monitoring.

  5. Pilot studies to achieve waste minimization and enhance radioactive liquid waste treatment at the Los Alamos National Laboratory Radioactive Liquid Waste Treatment Facility

    Energy Technology Data Exchange (ETDEWEB)

    Freer, J.; Freer, E.; Bond, A. [and others

    1996-07-01

    The Radioactive and Industrial Wastewater Science Group manages and operates the Radioactive Liquid Waste Treatment Facility (RLWTF) at the Los Alamos National Laboratory (LANL). The RLWTF treats low-level radioactive liquid waste generated by research and analytical facilities at approximately 35 technical areas throughout the 43-square-mile site. The RLWTF treats an average of 5.8 million gallons (21.8-million liters) of liquid waste annually. Clarifloculation and filtration is the primary treatment technology used by the RLWTF. This technology has been used since the RLWTF became operable in 1963. Last year the RLWTF achieved an average of 99.7% removal of gross alpha activity in the waste stream. The treatment process requires the addition of chemicals for the flocculation and subsequent precipitation of radionuclides. The resultant sludge generated during this process is solidified in drums and stored or disposed of at LANL.

  6. Solvent extraction of radionuclides from aqueous tank waste

    Energy Technology Data Exchange (ETDEWEB)

    Bonnesen, P.; Sachleben, R.; Moyer, B. [Oak Ridge National Lab., TN (United States)

    1996-10-01

    The purpose of this task is to develop an efficient solvent-extraction and stripping process to remove the fission products {sup 99}Tc, {sup 90}Sr, and {sup 137}Cs from alkaline tank waste, such as those stored at Hanford and Oak Ridge. As such, this task expands on FY 1995`s successful development of a solvent-extraction and stripping process for technetium separation from alkaline tank-waste solutions. This process now includes the capability of removing both technetium and strontium simultaneously. In this form, the process has been named SRTALK and will be developed further in this program as a prelude to developing a system capable of removing technetium, strontium, and cesium.

  7. Basic Ionic Liquid: A Reusable Catalyst for Knoevenagel Condensation in Aqueous Media

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    An efficient, environmentally friendly procedure was developed for the condensation of aldehydes/ketones and activated methylene compounds with basic ionic liquid as thecatalyst in water. This basic ionic liquid catalyst has a very high activity for Knoevenagel condensation to give the corresponding products in 70% -97% isolated yields under mild conditions. The basic ionic liquid catalyst in aqueous system can be reused for six times without any significant loss of activity.

  8. Sampling and analysis of radioactive liquid wastes and sludges in the Melton Valley and evaporator facility storage tanks at ORNL

    Energy Technology Data Exchange (ETDEWEB)

    Sears, M.B.; Botts, J.L.; Ceo, R.N.; Ferrada, J.J.; Griest, W.H.; Keller, J.M.; Schenley, R.L.

    1990-09-01

    The sampling and analysis of the radioactive liquid wastes and sludges in the Melton Valley Storage Tanks (MVSTs), as well as two of the evaporator service facility storage tanks at ORNL, are described. Aqueous samples of the supernatant liquid and composite samples of the sludges were analyzed for major constituents, radionuclides, total organic carbon, and metals listed as hazardous under the Resource Conservation and Recovery Act (RCRA). Liquid samples from five tanks and sludge samples from three tanks were analyzed for organic compounds on the Environmental Protection Agency (EPA) Target Compound List. Estimates were made of the inventory of liquid and sludge phases in the tanks. Descriptions of the sampling and analytical activities and tabulations of the results are included. The report provides data in support of the design of the proposed Waste Handling and Packaging Plant, the Liquid Low-Level Waste Solidification Project, and research and development activities (R D) activities in developing waste management alternatives. 7 refs., 8 figs., 16 tabs.

  9. Generation projection of solid and liquid radioactive wastes and spent radioactive sources in Mexico; Proyeccion de generacion de desechos radiactivos solidos, liquidos y fuentes radiactivas gastadas en Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Garcia A, E.; Hernandez F, I. Y.; Fernandez R, E. [Universidad Politecnica del Valle de Toluca, Km 5.7 Carretera Almoloya de Juarez, Estado de Mexico (Mexico); Monroy G, F.; Lizcano C, D., E-mail: fabiola.monroy@inin.gob.mx [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2014-10-15

    This work is focused to project the volumes of radioactive aqueous liquid wastes and spent radioactive sources that will be generated in our country in next 15 years, solids compaction and radioactive organic liquids in 10 years starting from the 2014; with the purpose of knowing the technological needs that will be required for their administration. The methodology involves six aspects to develop: the definition of general objectives, to specify the temporary horizon of projection, data collection, selection of the prospecting model and the model application. This approach was applied to the inventory of aqueous liquid wastes, as well as radioactive compaction organic and solids generated in Mexico by non energy applications from the 2001 to 2014, and of the year 1997 at 2014 for spent sources. The applied projection models were: Double exponential smoothing associating the tendency, Simple Smoothing and Lineal Regression. For this study was elected the first forecast model and its application suggests that: the volume of the compaction solid wastes, aqueous liquids and spent radioactive sources will increase respectively in 152%, 49.8% and 55.7%, while the radioactive organic liquid wastes will diminish in 13.15%. (Author)

  10. RECOVERY OF MERCURY FROM CONTAMINATED LIQUID WASTES

    Energy Technology Data Exchange (ETDEWEB)

    Robin M. Stewart

    1999-09-29

    Mercury was widely used in U.S. Department of Energy (DOE) weapons facilities, resulting in a broad range of mercury-contaminated wastes and wastewaters. Some of the mercury contamination has escaped to the local environment, particularly at the Y-12 Plant in Oak Ridge, Tennessee, where approximately 330 metric tons of mercury were discharged to the environment between 1953 and 1963 (TN & Associates, 1998). Effective removal of mercury contamination from water is a complex and difficult problem. In particular, mercury treatment of natural waters is difficult because of the low regulatory standards. For example, the Environmental Protection Agency has established a national ambient water quality standard of 12 parts-per-trillion (ppt), whereas the standard is 1.8 ppt in the Great Lakes Region. In addition, mercury in the environment is typically present in several different forms, but sorption processes are rarely effective with more than one or two of these forms. To meet the low regulatory discharge limits, an effective sorption process must be able to address all forms of mercury present in the water. One approach is to apply different sorbents in series depending on the mercury speciation and the regulatory discharge limits. ADA Technologies, Inc. has developed four new sorbents to address the variety of mercury species present in industrial discharges and natural waters. Three of these sorbents have been field tested on contaminated creek water at the Y-12 Plant. Two of these sorbents have been successfully demonstrated very high removal efficiencies for soluble mercury species, reducing mercury concentrations at the outlet of a pilot-scale system to less than 12 ppt for as long as six months. The other sorbent tested at the Y-12 Plant targeted colloidal mercury not removed by standard sorption or filtration processes. At the Y-12 Plant, colloidal mercury appears to be associated with iron, so a sorbent that removes mercury-iron complexes in the presence of a

  11. Using benchmarking to minimize common DOE waste streams. Volume 1, Methodology and liquid photographic waste

    Energy Technology Data Exchange (ETDEWEB)

    Levin, V.

    1994-04-01

    Finding innovative ways to reduce waste streams generated at Department of Energy (DOE) sites by 50% by the year 2000 is a challenge for DOE`s waste minimization efforts. This report examines the usefulness of benchmarking as a waste minimization tool, specifically regarding common waste streams at DOE sites. A team of process experts from a variety of sites, a project leader, and benchmarking consultants completed the project with management support provided by the Waste Minimization Division EM-352. Using a 12-step benchmarking process, the team examined current waste minimization processes for liquid photographic waste used at their sites and used telephone and written questionnaires to find ``best-in-class`` industrv partners willing to share information about their best waste minimization techniques and technologies through a site visit. Eastman Kodak Co., and Johnson Space Center/National Aeronautics and Space Administration (NASA) agreed to be partners. The site visits yielded strategies for source reduction, recycle/recovery of components, regeneration/reuse of solutions, and treatment of residuals, as well as best management practices. An additional benefit of the work was the opportunity for DOE process experts to network and exchange ideas with their peers at similar sites.

  12. Idaho Nuclear Technology and Engineering Center Newly Generated Liquid Waste Demonstration Project Feasibility Study

    Energy Technology Data Exchange (ETDEWEB)

    Herbst, A.K.

    2000-02-01

    A research, development, and demonstration project for the grouting of newly generated liquid waste (NGLW) at the Idaho Nuclear Technology and Engineering Center is considered feasible. NGLW is expected from process equipment waste, decontamination waste, analytical laboratory waste, fuel storage basin waste water, and high-level liquid waste evaporator condensate. The potential grouted waste would be classed as mixed low-level waste, stabilized and immobilized to meet RCRA LDR disposal in a grouting process in the CPP-604 facility, and then transported to the state.

  13. Boron Removal in Radioactive Liquid Waste by Forward Osmosis Membrane

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, Dooseong; Choi, Hei Min; Lee, Kune Woo; Moon Jeikwon [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2014-05-15

    These wastes contain about 0.3-0.8 wt% boric acid and have been concentrated through an evaporation treatment. Boric acid tends to crystallize owing to its solubility, and to plug the evaporator. The volume reduction obtained through evaporation is limited by the amount of boric acid in the waste. As an emerging technology, forward osmosis (FO) has attracted growing interest in wastewater treatment and desalination. FO is a membrane process in which water flows across a semi-permeable membrane from a feed solution of lower osmotic pressure to a draw solution of higher osmotic pressure. However, very few studies on the removal of boron by FO have been performed. The objective of this study is to evaluate the possibility of boron separation in radioactive liquid waste by FO. In this study, the performance of FO was investigated to separate boron in the simulated liquid waste under the factors such as pH, osmotic pressure, ionic strength of the solution, and membrane characteristic. The boron separation in radioactive borate liquid waste was investigated with an FO membrane. When the feed solution containing boron is treated by the FO membrane, the boron permeation depends on the type of membrane, membrane orientation, pH of the feed solution, salt and boron concentration in the feed solution, and osmotic pressure of the draw solution. The boron flux begins to decline from pH 7, and increases with an increase in the osmotic driving force. The boron flux of the CTA-ES and ALFD membrane orientation is higher than those of the CTA-NW and ALFF orientation, respectively. The boron permeation rate is constant regardless of the osmotic pressure and membrane orientation. The boron flux decreases slightly with the salt concentration, but it is not heavily influenced at a low salt concentration.

  14. RECOVERY OF CARBOXYLIC ACIDS FROM AQUEOUS SOLUTIONS BY LIQUID-LIQUID EXTRACTION WITH A TRIISOOCTYLAMINE DILUENT SYSTEM

    Directory of Open Access Journals (Sweden)

    G. Malmary

    2001-12-01

    Full Text Available Tertiary alkylamines in solution with organic diluents are attractive extractants for the recovery of carboxylic acids from dilute aqueous phases. The aim of this study was to investigate the mechanism for extraction of organic acids from water by a long-chain aliphatic tertiary amine. In order to attain this objective, we studied the liquid-liquid equilibria between the triisooctylamine + 1-octanol + n-heptane system as solvent and an aqueous solution of an individual carboxylic acid such as citric, lactic and malic acids. The experiments showed that the partition coefficient for a particular organic acid depends on the kind of solute, notably when the acid concentration in the aqueous phase is low. A mathematical model, where both chemical association and physical distribution are taken into consideration, is proposed. The model suggests that the various complexes obtained between amine and organic acids contribute to the distribution of the solute between the coexisting phases in equilibrium.

  15. Comparison of alkaline industrial wastes for aqueous mineral carbon sequestration through a parallel reactivity study.

    Science.gov (United States)

    Noack, Clinton W; Dzombak, David A; Nakles, David V; Hawthorne, Steven B; Heebink, Loreal V; Dando, Neal; Gershenzon, Michael; Ghosh, Rajat S

    2014-10-01

    Thirty-one alkaline industrial wastes from a wide range of industrial processes were acquired and screened for application in an aqueous carbon sequestration process. The wastes were evaluated for their potential to leach polyvalent cations and base species. Following mixing with a simple sodium bicarbonate solution, chemistries of the aqueous and solid phases were analyzed. Experimental results indicated that the most reactive materials were capable of sequestering between 77% and 93% of the available carbon under experimental conditions in four hours. These materials - cement kiln dust, spray dryer absorber ash, and circulating dry scrubber ash - are thus good candidates for detailed, process-oriented studies. Chemical equilibrium modeling indicated that amorphous calcium carbonate is likely responsible for the observed sequestration. High variability and low reactive fractions render many other materials less attractive for further pursuit without considering preprocessing or activation techniques.

  16. Development of tropine-salt aqueous two-phase systems and removal of hydrophilic ionic liquids from aqueous solution.

    Science.gov (United States)

    Wu, Haoran; Yao, Shun; Qian, Guofei; Song, Hang

    2016-08-26

    A novel aqueous two-phase systems (ATPS) composed of a small molecule organic compound tropine and an organic or inorganic salt aqueous solution has been developed for the first time. The phase behavior of tropine-salt ATPS was systemically investigated and the phase equilibrium data were measured in different temperatures and concentrations and correlated by the Merchuk equation with satisfactory results. The detection of the conductivity and particle size proved the formation of micelle in the process of forming tropine-salt ATPS. The separation application of the ATPS was assessed with the removal of hydrophilic benzothiazolium-based ionic liquids (ILs) from aqueous solution. The result showed that ILs were effectively extracted into the top tropine-rich phase. Finally, ILs in the top tropine-rich phase were further separated by the means of adsorption-desorption with DM301 macroporous resin and ethanol. The method of novel tropine-salt ATPS combined with adsorption-desorption is demonstrated a promising alternative thought and approach for the removal or recovery of hydrophilic compounds from aqueous media and also could provide a potential application for bio-separation.

  17. Dissociation of equimolar mixtures of aqueous carboxylic acids in ionic liquids: role of specific interactions.

    Science.gov (United States)

    Shukla, Shashi Kant; Kumar, Anil

    2015-04-30

    Hammett acidity function observes the effect of protonation/deprotonation on the optical density/absorbance of spectrophotometric indicator. In this work, the Hammett acidity, H0, of equimolar mixtures of aqueous HCOOH, CH3COOH, and CH3CH2COOH was measured in 1-methylimidazolium-, 1-methylpyrrolidinium-, and 1-methylpiperidinium-based protic ionic liquids (PILs) and 1-butyl-3-methylimidazolium-based aprotic ionic liquid (AIL) with formate (HCOO(-)) anion. Higher H0 values were observed for the equimolar mixtures of aqueous carboxylic acids in protic ionic liquids compared with those of the aprotic ionic liquid because of the involvement of the stronger specific interactions between the conjugate acid of ionic liquid and conjugate base of carboxylic acids as suggested by the hard-soft acid base (HSAB) theory. The different H0 values for the equimolar mixtures of aqueous carboxylic acids in protic and aprotic ionic liquids were noted to depend on the activation energy of proton transfer (Ea,H(+)). The higher activation energy of proton transfer was obtained in AIL, indicating lower ability to form specific interactions with solute than that of PILs. Thermodynamic parameters determined by the "indicator overlapping method" further confirmed the involvement of the secondary interactions in the dissociation of carboxylic acids. On the basis of the thermodynamic parameter values, the potential of different ionic liquids in the dissociation of carboxylic acids was observed to depend on the hydrogen bond donor acidity (α) and hydrogen bond acceptor basicity (β), characteristics of specific interactions.

  18. Removal of lead from aqueous solution using waste tire rubber ash as an adsorbent

    OpenAIRE

    Mousavi,H. Z.; Hosseynifar,A.; Jahed,V.; S. A. M. Dehghani

    2010-01-01

    The purpose of this study was to investigate the possibility of the utilization of waste tire rubber ash (WTRA) as a low cost adsorbent for removal of lead (II) ion from aqueous solution. The effect of different parameters (such as contact time, sorbate concentration, adsorbent dosage, pH of the medium and temperature) were investigated. The sorption process was relatively fast and equilibrium was reached after about 90 min of contact. The experimental data were analyzed by the Freundlich iso...

  19. Removal and recovery of toxic metal ions from aqueous waste sites using polymer pendant ligands

    Energy Technology Data Exchange (ETDEWEB)

    Fish, D. [Lawrence Berkeley National Lab., CA (United States)

    1996-10-01

    The purpose of this project is to investigate the use of polymer pendant ligand technology to remove and recover toxic metal ions from DOE aqueous waste sites. Polymer pendant lgiands are organic ligands, anchored to crosslinked, modified divinylbenzene-polystyrene beads, that can selectively complex metal ions. The metal ion removal step usually occurs through a complexation or ion exchange phenomena, thus recovery of the metal ions and reuse of the beads is readily accomplished.

  20. Aqueous liquid scintillation counting with fluor-containing nanosuspensions

    Energy Technology Data Exchange (ETDEWEB)

    Weekley, James C.; Wuenschel, Sara; Rosenstiel, Paul E.; Mumper, Russell J.; Jay, Michael E-mail: jay@email.uky.edu

    2004-06-01

    A microemulsion comprised of water, Brij 78, pentanol and styrene into which PPO and bis-MSB had been dissolved was prepared. Polymerization of the styrene resulted in a suspension of fluor-containing polystyrene nanoparticles (<100 nm). After a concentration step, the aqueous nanosuspension was able to detect {sup 14}C with counting efficiencies over 50% of those of a commercially available scintillation cocktail. Monte Carlo calculations demonstrated that the size and concentration of the nanoparticles were appropriate for optimum detection efficiency.

  1. LIQUID DYES'CHARACTERISTICS IN DYEING WASTE PAPER PULP AND THEIR APPLICATION

    Institute of Scientific and Technical Information of China (English)

    XiaopingWang; gangChen; AiminTang; HongweiZhang

    2004-01-01

    In this paper, some liquid dyes were used to dye the waste paper pulp (OCC pulp and waste cement sack paper pulp), and their dyeing characteristics were analyzed, The liquid dyes include liquid basic yellow, liquid basic blue, liquid basic red, liquid basic orange, liquid basic brown and liquid direct black. We found that, each dye had its own dyeing characteristic while dyeing the waste paper pulp. Generally different types of liquid dyes were combined to dye the waste paper pulp, which the adding process must be noticed. We also observed that a black pigment could be applied together withsaid liquid dyes to dye or adjust the color of the bottom sheet for the fireproof board. We could also achieve the same dyeing result through different combinations of different dyes.

  2. LIQUID DYES'CHARACTERISTICS IN DYEING WASTE PAPER PULP AND THEIR APPLICATION

    Institute of Scientific and Technical Information of China (English)

    Xiaoping Wang; gang Chen; Aimin Tang; Hongwei Zhang

    2004-01-01

    In this paper, some liquid dyes were used to dye the waste paper pulp (OCC pulp and waste cement sack paper pulp), and their dyeing characteristics were analyzed, The liquid dyes include liquid basic yellow, liquid basic blue, liquid basic red, liquid basic orange, liquid basic brown and liquid direct black. We found that, each dye had its own dyeing characteristic while dyeing the waste paper pulp.Generally different types of liquid dyes were combined to dye the waste paper pulp, which the adding process must be noticed. We also observed that a black pigment could be applied together with said liquid dyes to dye or adjust the color of the bottom sheet for the fireproof board. We could also achieve the same dyeing result through different combinations of different dyes.

  3. Modeling of Vapor-Liquid-Solid Equilibria in Acidic Aqueous Solutions

    DEFF Research Database (Denmark)

    Christensen, Søren Gregers; Thomsen, Kaj

    2003-01-01

    The phase behavior (vapor - liquid equilibria (VLE) and solid - liquid equilibria (SLE)) and thermal properties of aqueous solutions of ions like (K+, Na+, NH4+, Ca2+, Cl-) in the presence of phosphoric acid (H3PO4, H2PO4-, HPO42- ) and nitric acid (HNO3, NO3-) are described by means of the Exten......The phase behavior (vapor - liquid equilibria (VLE) and solid - liquid equilibria (SLE)) and thermal properties of aqueous solutions of ions like (K+, Na+, NH4+, Ca2+, Cl-) in the presence of phosphoric acid (H3PO4, H2PO4-, HPO42- ) and nitric acid (HNO3, NO3-) are described by means...

  4. The Effect of Liquid Crystalline Structures on Antiseizure Properties of Aqueous Solutions of Ethoxylated Alcohols

    OpenAIRE

    2010-01-01

    Aqueous solutions of ethoxylated alcohols which form lyotropic liquid crystals at high concentrations (40–80%) were selected as model lubricating substances. Microscopic studies under polarized light and viscosity measurements were carried out in order to confirm the presence of liquid crystalline structures in the case of alcohol solutions with ethoxylation degrees of 3, 5, 7 and 10. Microscopic images and viscosity coefficient values characteristic of various mesophases were obtained. As ex...

  5. Immobilization of Rose Waste Biomass for Uptake of Pb(II) from Aqueous Solutions.

    Science.gov (United States)

    Ansari, Tariq Mahmood; Hanif, Muhammad Asif; Mahmood, Abida; Ijaz, Uzma; Khan, Muhammad Aslam; Nadeem, Raziya; Ali, Muhammad

    2011-01-01

    Rosa centifolia and Rosa gruss an teplitz distillation waste biomass was immobilized using sodium alginate for Pb(II) uptake from aqueous solutions under varied experimental conditions. The maximum Pb(II) adsorption occurred at pH 5. Immobilized rose waste biomasses were modified physically and chemically to enhance Pb(II) removal. The Langmuir sorption isotherm and pseudo-second-order kinetic models fitted well to the adsorption data of Pb(II) by immobilized Rosa centifolia and Rosa gruss an teplitz. The adsorbed metal is recovered by treating immobilized biomass with different chemical reagents (H(2)SO(4), HCl and H(3)PO(4)) and maximum Pb(II) recovered when treated with sulphuric acid (95.67%). The presence of cometals Na, Ca(II), Al(III), Cr(III), Cr(VI), and Cu(II), reduced Pb(II) adsorption on Rosa centifolia and Rosa gruss an teplitz waste biomass. It can be concluded from the results of the present study that rose waste can be effectively used for the uptake of Pb(II) from aqueous streams.

  6. Corrosion behavior of technetium waste forms exposed to various aqueous environments

    Energy Technology Data Exchange (ETDEWEB)

    Kolman, David Gary [Los Alamos National Laboratory; Jarvinen, Gordon [Los Alamos National Laboratory; Mausolf, Edward [UNIV OF NEVADA; Czerwinski, Ken [UNIV OF NEVADA; Poineau, Frederic [UNIV OF NEVADA

    2009-01-01

    Technetium is a long-lived beta emitter produced in high yields from uranium as a waste product in spent nuclear fuel and has a high degree of environmental mobility as pertechnetate. It has been proposed that Tc be immobilized into various metallic waste forms to prevent Tc mobility while producing a material that can withstand corrosion exposed to various aqueous medias to prevent the leachability of Tc to the environment over long periods of time. This study investigates the corrosion behavior of Tc and Tc alloyed with 316 stainless steel and Zr exposed to a variety of aqueous media. To date, there is little investigative work related to Tc corrosion behavior and less related to potential Tc containing waste forms. Results indicate that immobilizing Tc into stainless steel-zirconium alloys can be a promising technique to store Tc for long periods of time while reducing the need to separately store used nuclear fuel cladding. Initial results indicate that metallic Tc and its alloys actively corrode in all media. We present preliminary corrosion rates of 100% Tc, 10% Tc - 90% SS{sub 85%}Zr{sub 15%}, and 2% Tc - 98% SS{sub 85%}Zr{sub 15%} in varying concentrations of nitric acid and pH 10 NaOH using the resistance polarization method while observing the trend that higher concentrations of Tc alloyed to the sample tested lowers the corrosion rate of the proposed waste package.

  7. Recovery of uranium and plutonium from Redox off-standard aqueous waste streams

    Energy Technology Data Exchange (ETDEWEB)

    Holm, C.H.; Matheson, A.R.

    1949-12-31

    In the operation of countercurrent extraction columns as in the Redox process, it is possible, and probable, that from unexpected behaviour of a column, operator error, colloid formation, etc., there will result from time to time excessive losses of uranium and plutonium in the overall process. These losses will naturally accumulate in the waste streams, particularly in the aqueous waste streams. If the loss is excessively high, and such lost material can be recovered by some additional method, then if economical and within reason, the recovered materials ran be returned to a ISF column for further processing. The objective of this work has been to develop such a method to recover uranium and plutonium from such off-standard waste streams in a form whereby the uranium send plutonium can be returned to the process line and subsequently purified and separated.

  8. Glass transition of aqueous solutions involving annealing-induced ice recrystallization resolves liquid-liquid transition puzzle of water.

    Science.gov (United States)

    Zhao, Li-Shan; Cao, Ze-Xian; Wang, Qiang

    2015-10-27

    Liquid-liquid transition of water is an important concept in condensed-matter physics. Recently, it was claimed to have been confirmed in aqueous solutions based on annealing-induced upshift of glass-liquid transition temperature, T(g) . Here we report a universal water-content, X(aqu) , dependence of T(g) for aqueous solutions. Solutions with X(aqu)>X(cr)(aqu)vitrify/devitrify at a constant temperature, ~T(g) , referring to freeze-concentrated phase with X(aqu)left behind ice crystallization. Those solutions with X(aqu)recrystallization is stabilized at . Experiments on aqueous glycerol and 1,2,4-butanetriol solutions in literature were repeated, and the same samples subject to other annealing treatments equally reproduce the result. The upshift of T(g) by annealing is attributable to freeze-concentrated phase of solutions instead of 'liquid II phase of water'. Our work also provides a reliable method to determine hydration formula and to scrutinize solute-solvent interaction in solution.

  9. Removal of cesium using coconut fiber in raw and modified forms for the treatment of radioactive liquid wastes

    Energy Technology Data Exchange (ETDEWEB)

    Jesus, Nella N.M. de; Nobre, Vanessa B.; Potiens Junior, Ademar J.; Sakata, Solange K., E-mail: sksakata@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Di Vitta, Patricia B. [Universidade de Sao Paulo (USP), SP (Brazil). Instituto de Quimica

    2013-07-01

    Sorption is one of the most studied methods to reduce the volume of radioactive waste streams. Cesium-137 is a radioisotope formed by the fission of uranium and it can cause health problems due to its easy assimilation by cells. The aim of this study is to evaluate the potential of coconut fiber in removing cesium from radioactive liquid wastes; this process can help in disposing radioactive waste. The experiments were performed in batch and the particle size of the fiber ranged between 0.30 mm and 0.50 mm. The fiber was treated with hydrogen peroxide in alkaline medium. The following parameters were analyzed: contact time, pH and concentration of cesium ions in aqueous solution. After the experiments the samples were filtered and cesium remaining in solution was quantified by inductively coupled plasma optical emission spectrometry. (author)

  10. Modeling of vapor-liquid-solid equilibrium in gas - aqueous electrolyte systems

    DEFF Research Database (Denmark)

    Thomsen, Kaj; Rasmussen, Peter

    1999-01-01

    A thermodynamic model for the description of vapor-liquid-solid equilibria is introduced. This model is a combination of the extended UNIQUAC model for electrolytes and the Soave-Redlich-Kwong cubic equation of state. The model has been applied to aqueous systems containing ammonia and/or carbon...

  11. Effects of solid-liquid separation and storage on monensin attenuation in dairy waste management systems

    Science.gov (United States)

    Hafner, Sarah C.; Watanabe, Naoko; Harter, Thomas; Bergamaschi, Brian; Parikh, Sanjai J.

    2017-01-01

    Environmental release of veterinary pharmaceuticals has been of regulatory concern for more than a decade. Monensin is a feed additive antibiotic that is prevalent throughout the dairy industry and is excreted in dairy waste. This study investigates the potential of dairy waste management practices to alter the amount of monensin available for release into the environment. Analysis of wastewater and groundwater from two dairy farms in California consistently concluded that monensin is most present in lagoon water and groundwater downgradient of lagoons. Since the lagoons represent a direct source of monensin to groundwater, the effect of waste management, by mechanical screen separation and lagoon aeration, on aqueous monensin concentration was investigated through construction of lagoon microcosms. The results indicate that monensin attenuation is not improved by increased solid-liquid separation prior to storage in lagoons, as monensin is rapidly desorbed after dilution with water. Monensin is also shown to be easily degraded in lagoon microcosms receiving aeration, but is relatively stable and available for leaching under typical anaerobic lagoon conditions.

  12. Effects of solid-liquid separation and storage on monensin attenuation in dairy waste management systems.

    Science.gov (United States)

    Hafner, Sarah C; Watanabe, Naoko; Harter, Thomas; Bergamaschi, Brian A; Parikh, Sanjai J

    2017-04-01

    Environmental release of veterinary pharmaceuticals has been of regulatory concern for more than a decade. Monensin is a feed additive antibiotic that is prevalent throughout the dairy industry and is excreted in dairy waste. This study investigates the potential of dairy waste management practices to alter the amount of monensin available for release into the environment. Analysis of wastewater and groundwater from two dairy farms in California consistently concluded that monensin is most present in lagoon water and groundwater downgradient of lagoons. Since the lagoons represent a direct source of monensin to groundwater, the effect of waste management, by mechanical screen separation and lagoon aeration, on aqueous monensin concentration was investigated through construction of lagoon microcosms. The results indicate that monensin attenuation is not improved by increased solid-liquid separation prior to storage in lagoons, as monensin is rapidly desorbed after dilution with water. Monensin is also shown to be easily degraded in lagoon microcosms receiving aeration, but is relatively stable and available for leaching under typical anaerobic lagoon conditions.

  13. Liquid high-level waste storage - can we tolerate it?

    Energy Technology Data Exchange (ETDEWEB)

    Taylor, P. [Terramares Group (United Kingdom)

    1996-12-31

    High-level radioactive waste from reprocessing is stored at British Nuclear Fuel`s Sellafield site in High Active Storage Tanks (HAST`s), which require constant cooling and ventilation. The author argues that, containing as they do, about 100 times the caesium 137 released during the Chernobyl accident, these containment tanks represent an unacceptably high risk of a major release of caesium 137, a volatile gamma-emitter with a half-life of about 30 years. It is readily transferred into food chains and difficult to remove from soils, tarmac and concrete. Still worse, it is argued, are the tens of thousands of cancers and other biological radiation effects likely to occur as a result of such a release. He argues for the vitrification of all such highly active liquid wastes, which would slow further reprocessing down to accommodate the current backlog. (UK).

  14. Aqueous solutions of acidic ionic liquids for enhanced stability of polyoxometalate-carbon supercapacitor electrodes

    Science.gov (United States)

    Hu, Chenchen; Zhao, Enbo; Nitta, Naoki; Magasinski, Alexandre; Berdichevsky, Gene; Yushin, Gleb

    2016-09-01

    Nanocomposites based on polyoxometalates (POMs) nanoconfined in microporous carbons have been synthesized and used as electrodes for supercapacitors. The addition of the pseudocapacitance from highly reversible redox reaction of POMs to the electric double-layer capacitance of carbon lead to an increase in specific capacitance of ∼90% at 1 mV s-1. However, high solubility of POM in traditional aqueous electrolytes leads to rapid capacity fading. Here we demonstrate that the use of aqueous solutions of protic ionic liquids (P-IL) as electrolyte instead of aqueous sulfuric acid solutions offers an opportunity to significantly improve POM cycling stability. Virtually no degradation in capacitance was observed in POM-based positive electrode after 10,000 cycles in an asymmetric capacitor with P-IL aqueous electrolyte. As such, POM-based carbon composites may now present a viable solution for enhancing energy density of electrical double layer capacitors (EDLC) based on pure carbon electrodes.

  15. Tea Wastes Efficiency on Removal of Cd(II From Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Mehrdad Cheraghi

    2016-07-01

    Full Text Available Background & Aims of the Study: Heavy metals, such as cadmium (Cd(II, enter into the environment and cause health hazard due to their toxicity and bioaccumulation in the human body. Therefore, they must be removed from water. In recent years, much attention has been focused on the use of material residues as low-cost adsorbents for the removal of heavy metal ions from aqueous solutions. The aim of this paper is the assessment of tea wastes efficiency on removal of Cd(II from aqueous solutions. Materials and Methods: The present study was conducted in experimental scale. In this paper, tea wastes were prepared and used as an adsorbent for the removal of Cd(II ions from water. In batch tests, the effect of parameters like pH (1.0-8.0, initial metal concentration (100-800 mg L-1, contact time (15-120 min, adsorbent dose (1.0-5.0 g and temperature (25-55 °C on the adsorption process was studied. Results: The results demonstrated that the maximum percentage of Cd(II adsorption was found at pH 6.0 and the equilibrium was achieved after 60 min with 3.0 g tea wastes. The experimental isotherm data were analyzed, using the Langmuir and Freundlich models and it was found that the removal process followed the Langmuir isotherm. In addition, the adsorption kinetics followed the pseudo-second-order kinetic model. The maximum adsorption capacity calculated by Langmuir fitting was 71.4 mg g−1. Conclusion: The results suggest that tea wastes could be employed as an effective material for the removal of Cd(II ions from aqueous solutions and the maximum adsorption capacity was found to be 71.4 mg g−1.

  16. Processing liquid organic wastes at the NNL Preston laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Coppersthwaite, Duncan; Greenwood, Howard; Docrat, Tahera; Allinson, Sarah; Sultan, Ruqayyah; May, Sarah [National Nuclear Laboratory Preston, Lancashire (United Kingdom)

    2013-07-01

    Organic compounds of various kinds have been used in the nuclear industry for numerous duties in uranium chemical, metal and ceramic processing plants. In the course of the various operations undertaken, these organic compounds have become contaminated with uranic material, either accidentally or as an inevitable part of the process. Typically, the chemical/physical form and/or concentration of the uranic content of the organics has prevented disposal. In order to address the issue of contaminated liquid organic wastes, the National Nuclear Laboratory (NNL) has developed a suite of treatments designed to recover uranium and to render the waste suitable for disposal. The developed processes are operated at industrial scale via the NNL Preston Laboratory Residue Processing Plant. The Oil Waste Leaching (OWL) Process is a fully industrialised process used for the treatment of contaminated oils with approximately 200 tonnes of uranium contaminated oil being treated to date. The process was originally developed for the treatment of contaminated tributyl phosphate and odourless kerosene which had been adsorbed onto sawdust. However, over the years, the OWL process has been refined for a range of oils including 'water emulsifiable' cutting oils, lubricating oils, hydraulic oils/fluids and 'Fomblin' (fully fluorinated) oils. Chemically, the OWL process has proved capable of treating solvents as well as oils but the highly volatile/flammable nature of many solvents has required additional precautions compared with those required for oil treatment. These additional precautions led to the development of the Solvent Treatment Advanced Rig (STAR), an installation operated under an inert atmosphere. STAR is a small 'module' (100 dm{sup 3} volume) which allows the treatment of both water miscible and immiscible solvents. This paper discusses the challenges associated with the treatment of liquid organic wastes and the process developments which have

  17. Effect of liquid waste discharges from steam generating facilities

    Energy Technology Data Exchange (ETDEWEB)

    McGuire, H.E. Jr.

    1977-09-01

    This report contains a summary of the effects of liquid waste discharges from steam electric generating facilities on the environment. Also included is a simplified model for use in approximately determining the effects of these discharges. Four basic fuels are used in steam electric power plants: three fossil fuels--coal, natural gas, and oil; and uranium--presently the basic fuel of nuclear power. Coal and uranium are expected to be the major fuels in future years. The following power plant effluents are considered: heat, chlorine, copper, total dissolved solids, suspended solids, pH, oil and grease, iron, zinc, chrome, phosphorus, and trace radionuclides.

  18. Selion offers a unique system for treating liquid nuclear waste

    Energy Technology Data Exchange (ETDEWEB)

    Tusa, E.; Kurki, H. [ed.

    1998-07-01

    Studies on the treatment of liquid nuclear waste have been conducted actively in the IVO Group since the early 1980s. And the work has borne fruit: the CsTreat and SrTreat ion exchange products, developed by the IVO Group, were launched three years ago. The ion exchangers have already been in full use at a number of sites throughout the world. In addition, they are currently being tested at many nuclear research institutes and power plants in the USA, Japan and Europe

  19. Bilayer membrane permeability of ionic liquid-filled block copolymer vesicles in aqueous solution.

    Science.gov (United States)

    Bai, Zhifeng; Zhao, Bin; Lodge, Timothy P

    2012-07-19

    The bilayer membrane permeability of block copolymer vesicles ("polymersomes") with ionic liquid interiors dispersed in water is quantified using fluorescence quenching. Poly((1,2-butadiene)-b-ethylene oxide) (PB-PEO) block copolymer vesicles in water with their interiors filled with a common hydrophobic ionic liquid, 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide, were prepared containing a hydrophobic dye, Nile Red, by intact migration of dye-encapsulated vesicles from the ionic liquid to water at room temperature. A small quencher molecule, dichloroacetamide, was added to the aqueous solution of the dye-loaded vesicles, and the permeation of the quencher passing through the membrane into the interior was determined from the fluorescence quenching kinetics. Rapid permeation of the quencher across the nanoscale membrane was observed, consistent with the high fluidity of the liquid polybutadiene membrane. Two different PB-PEO copolymers were employed, in order to vary the thickness of the solvophobic membrane. A significant increase in membrane permeability was also observed with decreasing membrane thickness, which is tentatively attributable to differences in quencher solubility in the membranes. Quantitative migration of the vesicles from the aqueous phase back to an ionic liquid phase was achieved upon heating. These microscopically heterogeneous and thermoresponsive vesicles with permeable and robust membranes have potential as recyclable nanoreactors, in which the high viscosity and capital expense of an ionic liquid reaction medium can be mitigated, while retaining the desirable features of ionic liquids as reaction media, and facile catalyst recovery.

  20. Low-temperature liquid-liquid extraction of phenols from aqueous solutions with hydrophilic mixtures of extractants

    Science.gov (United States)

    Rudakov, O. B.; Khorokhordina, E. A.; Preobrazhenskii, M. A.; Rudakova, L. V.

    2016-08-01

    The volume ratios in acetonitrile-ethyl acetate (90 : 10, 95 : 5), acetonitrile-isopropanol-ethyl acetate (70 : 15 : 15, 80 : 5 : 15), and isopropanol-1-butanol (50 : 50) mixtures were determined. Their mixing with water (1 : 1) and storage at-10°C led to partitioning into two immiscible liquid phases without formation of the ice phase. The mixtures were shown to be useful as hydrophilic extractants in low-temperature liquidliquid extraction of phenol from aqueous solutions.

  1. Effect of Na2O on aqueous dissolution of nuclear waste glasses

    Science.gov (United States)

    Farooqi, Rahmat Ullah; Hrma, Pavel

    2017-04-01

    Sodium oxide is present in the majority of commercial and waste glasses as a viscosity-reducing component. In some nuclear waste glasses, its source is the waste itself. As such, it can limit the waste loading because of its deleterious effect on the resistance of the glass to attack by aqueous media. The maximum tolerable content of Na2O in glass depends on the presence and concentration of components that interact with it. To assess the acceptability limits of Na2O in the composition region of nuclear waste glasses, we formulated 11 baseline compositions by varying the content of oxides of Si, B, Al, Ca, Zr, and Li. In each of these compositions, we varied the Na2O fraction from 8-16 mass% to 23-30 mass%. To each of 146 glasses thus formulated, we applied the seven-day Product Consistency Test (PCT) to determine normalized B and Na releases (ri, where i ≡ B or Na). Fitting approximation functions ln(ri/gm-2) = Σbijgj to ri data (gj is the j-th component mass fraction and bij the corresponding component coefficient), we showed that the rB (and, consequently, the initial glass alteration rate) was proportional to the glass component mass fractions in the order Al2O3role that PCT data may play in understanding the evolution of the glass alteration process is discussed.

  2. Aqueous nitrate waste treatment: Technology comparison, cost/benefit, and market analysis

    Energy Technology Data Exchange (ETDEWEB)

    1994-01-01

    The purpose of this analysis is to provide information necessary for the Department of Energy (DOE) to evaluate the practical utility of the Nitrate to Ammonia and Ceramic or Glass (NAC/NAG/NAX) process, which is under development in the Oak Ridge National Laboratory. The NAC/NACx/NAX process can convert aqueous radioactive nitrate-laden waste to a glass, ceramic, or grout solid waste form. The tasks include, but are not limited to, the following: Identify current commercial technologies to meet hazardous and radiological waste disposal requirements. The technologies may be thermal or non-thermal but must be all inclusive (i.e., must convert a radionuclide-containing nitrate waste with a pH around 12 to a stable form that can be disposed at permitted facilities); evaluate and compare DOE-sponsored vitrification, grouting, and minimum additive waste stabilization projects for life-cycle costs; compare the technologies above with respect to material costs, capital equipment costs, operating costs, and operating efficiencies. For the NAC/NAG/NAX process, assume aluminum reactant is government furnished and ammonia gas may be marketed; compare the identified technologies with respect to frequency of use within DOE for environmental management applications with appropriate rationale for use; Assess the potential size of the DOE market for the NAC/NAG/NAX process; assess and off-gas issues; and compare with international technologies, including life-cycle estimates.

  3. Research program on development of advanced treatment technology for americium-containing aqueous waste in NUCEF

    Energy Technology Data Exchange (ETDEWEB)

    Mineo, Hideaki; Matsumura, Tatsuro; Tsubata, Yasuhiro [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    1996-10-01

    A research program was prepared on the development of an advanced treatment process for the americium-containing concentrated aqueous waste in NUCEF, than allows americium recovery for the reuse and the reduction of TRU waste generation. A preliminary analysis was conducted on the separation requirements based on the components estimated for the waste. An R and D strategy was proposed from the view to reduce TRU waste generated in the processing that the highest priority is given on the control of TRU leakage such as americium into the effluent stream after americium recovery and the minimization of salt used in the separation over the decontamination of impurities from americium. The extraction chromatographic method was selected as a candidate technology for americium separation under the principle to use reagents that are functional in acidic conditions such as bidentate extractants of DHEDECMP, CMPO or diamides, considering the larger flexibilities in process modification and possible multi-component separation with compact equipment and the past achievements on the recovery of kg quantities of americium. Major R and D items extracted are screening and evaluation of extractants for americium and plutonium, optimization of separation conditions, selection of denitration method, equipment developments and development of solidification methods of discarded americium after reuse and of various kinds of separation residues. In order to cope these items, four steps of R and D program were proposed, i.e., fundamental experiment in beaker-scale on screening and evaluation of extractants, flowsheet study in bench-scale using simulated and small amount of americium aqueous waste solution to evaluate candidate process, americium recovery test in iron-shielded cell to be installed in NUCEF. It is objected to make recovery of 100g orders of americium used for research on fundamental TRU fuel properties. (J.P.N.)

  4. Removal of Pb (II from Aqueous Solutions Using Waste Tea Leaves

    Directory of Open Access Journals (Sweden)

    Mehrdad Cheraghi

    2015-03-01

    Full Text Available Background: The presence of lead in natural waters has become an important issue around the world. Lead has been identified as a highly toxic metal that can cause severe environmental and public health problems and its decontamination is of utmost importance. The aim of this work was to evaluate the adsorption of lead (Pb(II on waste tea leaves as a cheap purification method. Methods: In this experimental study, prepared waste tea leaves were used as adsorbent for the removal of Pb (II from aqueous solutions. Adsorption experiments were carried out as batch studies at different contact time, pH, amount of adsorbent, initial metal concentration and temperature. Results: The results showed that maximum removal efficiency was observed at pH 6. Also the adsorption of Pb (II ions increased with decreasing initial metal concentration. The Langmuir isotherm model fits well with the equilibrium adsorption isotherm data and its calculated maximum monolayer adsorption capacity was 166.6 mg g-1 at a temperature of 25±0.1˚C. The kinetic data obtained have been analyzed using pseudo-first-order and pseudo-second-order models. The best fitted kinetic model was found to be pseudo-second-order. Conclusion: The results suggest that tea wastes could be employed as cheap material for the removal of lead from aqueous solutions.

  5. Removal of methylene blue from aqueous solution using cotton stalk, cotton waste and cotton dust

    Energy Technology Data Exchange (ETDEWEB)

    Ertas, Murat [Department of Forest Industrial Engineering, Faculty of Forestry, Kahramanmaras Sutcu Imam University, 46060 Kahramanmaras (Turkey); Acemioglu, Bilal, E-mail: acemioglu@kilis.edu.tr [Department of Chemistry, Faculty of Science and Arts, Kilis 7 Aralik University, 79000 Kilis (Turkey); Alma, M. Hakki [Department of Forest Industrial Engineering, Faculty of Forestry, Kahramanmaras Sutcu Imam University, 46060 Kahramanmaras (Turkey); Usta, Mustafa [Department of Forest Industrial Engineering, Faculty of Forestry, Karadeniz Technical University, 61080 Trabzon (Turkey)

    2010-11-15

    In this study, cotton stalk (CS), cotton waste (CW) and cotton dust (CD) was used as sorbents to remove methylene blue (MB) from aqueous solution by batch sorption technique. Effects of initial dye concentration, solution pH, solution temperature and sorbent dose on sorption were studied. It was seen that the removal of methylene blue increased with increasing initial dye concentration (from 25 to 100 mg/l), solution pH (from 5 to 10), solution temperature (from 20 to 50 deg. C) and sorbent dose (from 0.25 to 1.50 g/50 ml). The maximum dye removal was reached at 90 min. Sorption isotherms were analyzed by Langmuir and Freundlich models at different temperatures of 20, 30, 40 and 50 deg. C, and the results were discussed in detail. Moreover, the thermodynamics of sorption were also studied. It was found that the values of standard free energy ({Delta}G{sup o}) were positive for cotton stalk and negative for cotton waste and cotton dust. The values of standard enthalpy ({Delta}H{sup o}) and entropy ({Delta}S{sup o}) were found to be positive, and the obtained results were interpreted in detail. The results of this study showed that cotton stalk, cotton waste and cotton dust could be employed as effective and low-cost materials for the removal of dyes from aqueous solution.

  6. Real-time alpha monitoring of a radioactive liquid waste stream at Los Alamos National Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, J.D.; Whitley, C.R.; Rawool-Sullivan, M. [Los Alamos National Lab., NM (United States)

    1995-12-31

    This poster display concerns the development, installation, and testing of a real-time radioactive liquid waste monitor at Los Alamos National Laboratory (LANL). The detector system was designed for the LANL Radioactive Liquid Waste Treatment Facility so that influent to the plant could be monitored in real time. By knowing the activity of the influent, plant operators can better monitor treatment, better segregate waste (potentially), and monitor the regulatory compliance of users of the LANL Radioactive Liquid Waste Collection System. The detector system uses long-range alpha detection technology, which is a nonintrusive method of characterization that determines alpha activity on the liquid surface by measuring the ionization of ambient air. Extensive testing has been performed to ensure long-term use with a minimal amount of maintenance. The final design was a simple cost-effective alpha monitor that could be modified for monitoring influent waste streams at various points in the LANL Radioactive Liquid Waste Collection System.

  7. Removal of lead from aqueous solution using waste tire rubber ash as an adsorbent

    Directory of Open Access Journals (Sweden)

    H. Z. Mousavi

    2010-03-01

    Full Text Available The purpose of this study was to investigate the possibility of the utilization of waste tire rubber ash (WTRA as a low cost adsorbent for removal of lead (II ion from aqueous solution. The effect of different parameters (such as contact time, sorbate concentration, adsorbent dosage, pH of the medium and temperature were investigated. The sorption process was relatively fast and equilibrium was reached after about 90 min of contact. The experimental data were analyzed by the Freundlich isotherm and the Langmuir isotherm. Equilibrium data fitted well with the Langmuir model with maximum adsorption capacity of 22.35 mg/g. The adsorption kinetics was investigated and the best fit was achieved by a first-order equation. The results of the removal process show that the Pb (II ion adsorption on WTRA is an endothermic and spontaneous process. The procedure developed was successfully applied for the removal of lead ions in aqueous solutions.

  8. Usefulness of Activated Carbon Prepared from Industrial Wastes in the Removal of Nickel from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    R. Rajalakshmi

    2009-01-01

    Full Text Available Elimination of heavy metals like nickel from waste water is an important subject in view of public health. In the present study, an attempt has been made to study the applicability of industrial by-products as potential metal adsorbents to remove nickel from aqueous solutions and polluted water. A direct proportionality between the percentage of Ni(II removal and adsorbent dosage was noted. Maximum removal ⁄ recovery of nickel was achieved at pH range of 10-12 for all adsorbents. An optimum temperature of 40 °C for efficient removal of Ni(II was observed. The effect of nickel adsorption was affected by salinity. The adsorption isotherm data confirmed to Freundlich and Langmuir isotherms. Conformation of data to the Lagergren᾽s rate equation indicated first order kinetics. The suitability of the industrial by-products in the successful removal of nickel from aqueous solution is quite obvious from the study.

  9. Production of furfural from waste aqueous hemicellulose solution of hardwood over ZSM-5 zeolite.

    Science.gov (United States)

    Gao, Hongling; Liu, Haitang; Pang, Bo; Yu, Guang; Du, Jian; Zhang, Yuedong; Wang, Haisong; Mu, Xindong

    2014-11-01

    This study aimed to produce furfural from waste aqueous hemicellulose solution of a hardwood kraft-based dissolving pulp production processing in a green method. The maximum furfural yield of 82.4% and the xylose conversion of 96.8% were achieved at 463K, 1.0g ZSM-5, 1.05g NaCl and organic solvent-to-aqueous phase ratio of 30:15 (V/V) for 3h. The furfural yield was just 51.5% when the same concentration of pure xylose solution was used. Under the optimized condition, furfural yield was still up to 67.1% even after the fifth reused of catalyst. Catalyst recycling study showed that ZSM-5 has a certain stability and can be efficiently reused.

  10. Getters for Tc and I Removal from Liquid Waste

    Science.gov (United States)

    Qafoku, N. P.; Asmussen, M.; Lawter, A.; Neeway, J.; Smith, G.

    2015-12-01

    A cementitious waste form, Cast Stone, is being evaluated as a possible supplemental waste form for the low activity waste (LAW) at the Hanford Site, which contains significant amounts of radioactive 99Tc and 129I, as part of the tank waste cleanup mission. To improve the retention of Tc and/or I in Cast Stone, materials with a high affinity for Tc and/or I, termed "getters," can be added to decrease the rate of contaminant release and diffusivity, and improve Cast Stone performance. A series of kinetic batch sorption experiments was performed to determine the effectiveness of the getter materials. Several Tc getters [blast furnace slag, Sn (II) apatite, SnCl2, nanoporous Sn phosphate, KMS-2 (a potassium-metal-sulfide), and Sn(II) hydroxyapatite] and I getters [layered Bi hydroxide, natural argentite mineral, synthetic argentite, Ag-impregnated carbon, and Ag-exchanged zeolite] were tested in different solution media, 18.2 MΩ DI H2O and a caustic LAW waste simulant containing 6.5 M Na or 7.8 M Na. The experiments were conducted at room temperature in the presence or absence of air. Results indicated that most Tc getters (with the exception of KMS-2) performed better in the DI H2O solution than in the 6.5 and 7.8 M Na LAW simulant. In addition, Tc sequestration may be affected by the presence of other redox sensitive elements that were present in the LAW simulant, such as Cr. The Tc getter materials have been examined through various solid-state characterization techniques such as XRD, SEM/EDS, XANES and EXAFS which provided evidence for plausible mechanisms of aqueous Tc removal. The results indicated that the Tc precipitates differ depending on the getter material and that Tc(VII) is reduced to Tc(IV) in most of the getters but to a differing extents. For the I getters, Ag-exchanged zeolite and synthetic argentite were the most effective ones. The other I getters showed limited effectiveness for sorbing I under the high ionic strength and caustic conditions of

  11. Aqueous reactive species induced by a surface air discharge: Heterogeneous mass transfer and liquid chemistry pathways

    Science.gov (United States)

    Liu, D. X.; Liu, Z. C.; Chen, C.; Yang, A. J.; Li, D.; Rong, M. Z.; Chen, H. L.; Kong, M. G.

    2016-01-01

    Plasma-liquid interaction is a critical area of plasma science and a knowledge bottleneck for many promising applications. In this paper, the interaction between a surface air discharge and its downstream sample of deionized water is studied with a system-level computational model, which has previously reached good agreement with experimental results. Our computational results reveal that the plasma-induced aqueous species are mainly H+, nitrate, nitrite, H2O2 and O3. In addition, various short-lived aqueous species are also induced, regardless whether they are generated in the gas phase first. The production/loss pathways for aqueous species are quantified for an air gap width ranging from 0.1 to 2 cm, of which heterogeneous mass transfer and liquid chemistry are found to play a dominant role. The short-lived reactive oxygen species (ROS) and reactive nitrogen species (RNS) are strongly coupled in liquid-phase reactions: NO3 is an important precursor for short-lived ROS, and in turn OH, O2− and HO2 play a crucial role for the production of short-lived RNS. Also, heterogeneous mass transfer depends strongly on the air gap width, resulting in two distinct scenarios separated by a critical air gap of 0.5 cm. The liquid chemistry is significantly different in these two scenarios. PMID:27033381

  12. Aqueous reactive species induced by a surface air discharge: Heterogeneous mass transfer and liquid chemistry pathways.

    Science.gov (United States)

    Liu, D X; Liu, Z C; Chen, C; Yang, A J; Li, D; Rong, M Z; Chen, H L; Kong, M G

    2016-04-01

    Plasma-liquid interaction is a critical area of plasma science and a knowledge bottleneck for many promising applications. In this paper, the interaction between a surface air discharge and its downstream sample of deionized water is studied with a system-level computational model, which has previously reached good agreement with experimental results. Our computational results reveal that the plasma-induced aqueous species are mainly H(+), nitrate, nitrite, H2O2 and O3. In addition, various short-lived aqueous species are also induced, regardless whether they are generated in the gas phase first. The production/loss pathways for aqueous species are quantified for an air gap width ranging from 0.1 to 2 cm, of which heterogeneous mass transfer and liquid chemistry are found to play a dominant role. The short-lived reactive oxygen species (ROS) and reactive nitrogen species (RNS) are strongly coupled in liquid-phase reactions: NO3 is an important precursor for short-lived ROS, and in turn OH, O2(-) and HO2 play a crucial role for the production of short-lived RNS. Also, heterogeneous mass transfer depends strongly on the air gap width, resulting in two distinct scenarios separated by a critical air gap of 0.5 cm. The liquid chemistry is significantly different in these two scenarios.

  13. Behavior of Supercooled Aqueous Solutions Stemming from Hidden Liquid-Liquid Transition in Water

    OpenAIRE

    Biddle, John W.; Holten, Vincent; Anisimov, Mikhail A.

    2014-01-01

    A popular hypothesis that explains the anomalies of supercooled water is the existence of a metastable liquid-liquid transition hidden below the line of homogeneous nucleation. If this transition exists and if it is terminated by a critical point, the addition of a solute should generate a line of liquid-liquid critical points emanating from the critical point of pure metastable water. We have analyzed thermodynamic consequences of this scenario. In particular, we consider the behavior of two...

  14. Influence of surfactant tail branching and organization on the orientation of liquid crystals at aqueous-liquid crystal interfaces.

    Science.gov (United States)

    Lockwood, Nathan A; de Pablo, Juan J; Abbott, Nicholas L

    2005-07-19

    We have examined the influence of two aspects of surfactant structure--tail branching and tail organization--on the orientational ordering (so-called anchoring) of water-immiscible, thermotropic liquid crystals in contact with aqueous surfactant solutions. First, we evaluated the influence of branches in surfactant tails on the anchoring of nematic liquid crystals at water-liquid crystal interfaces. We compared interfaces that were laden with one of three linear surfactants (sodium dodecyl sulfate, sodium dodecanesulfonate, and isomerically pure linear sodium dodecylbenzenesulfonate) to interfaces laden with branched sodium dodecylbenzenesulfonate. We carried out these experiments at 60 degrees C, above the Krafft temperatures of all the surfactants studied, and used the liquid crystal TL205 (a mixture of cyclohexane-fluorinated biphenyls and fluorinated terphenyls), which forms a nematic phase at 60 degrees C. Linear surfactants caused TL205 to assume a perpendicular orientation (homeotropic anchoring) above a threshold concentration of surfactant and parallel orientation (planar anchoring) at lower concentrations. In contrast, branched sodium dodecylbenzenesulfonate caused planar anchoring of TL205 at all concentrations up to the critical micelle concentration of the surfactant. Second, we used sodium dodecanesulfonate and a commercial linear sodium dodecylbenzenesulfonate to probe the influence of surfactant tail organization on the orientations of liquid crystals at water-liquid crystal interfaces. Commercial linear sodium dodecylbenzenesulfonate, which comprises a mixture of ortho and para isomers, has been previously characterized to form less ordered monolayers than sodium dodecanesulfonate at oil-water interfaces at room temperature. We found sodium dodecanesulfonate to cause homeotropic anchoring of both TL205 and 4'-pentyl-4-cyanobiphenyl (5CB, nematic at room temperature), whereas commercial linear sodium dodecylbenzenesulfonate caused predominantly

  15. Innovative Process for Comprehensive Treatment of Liquid Radioactive Waste - 12551

    Energy Technology Data Exchange (ETDEWEB)

    Penzin, R.A.; Sarychev, G.A. [All-Russia Scientific Research Institute of Chemical Technology (VNIIKHT), Moscow, 115409 (Russian Federation)

    2012-07-01

    ;Fukushima-1', personnel faces the necessity to take emergency measures and to use marine water for cooling of reactor zone in contravention of the technological regulations. In these cases significant amount of liquid radioactive wastes of complex physicochemical composition is being generated, the purification of which by traditional methods is close to impossible. According to the practice of elimination of the accident after-effects at NPP 'Fukushima' there are still no technical means for the efficient purification of liquid radioactive wastes of complex composition like marine water from radionuclides. Therefore development of state-of-the-art highly efficient facilities capable of fast and safe purification of big amounts of liquid radioactive wastes of complex physicochemical composition from radionuclides turns to be utterly topical problem. Cesium radionuclides, being extremely dangerous for the environment, present over 90% of total radioactivity contained in liquid radioactive wastes left as a result of accidents at nuclear power objects. For the purpose of radiation accidents aftereffects liquidation VNIIHT proposes to create a plant for LRW reprocessing, consisting of 4 major technological modules: Module of LRW pretreatment to remove mechanical and organic impurities including oil products; Module of sorption purification of LWR by means of selective inorganic sorbents; Module of reverse osmotic purification and desalination; Module of deep evaporation of LRW concentrates. The first free modules are based on completed technological and designing concepts implemented by VNIIHT in the framework of LLRW Project in the period of 2000-2001 in Russia for comprehensive treatment of LWR of atomic fleet. These industrial plants proved to be highly efficient and secure during their long operation life. Module of deep evaporation is a new technological development. It will ensure conduction of evaporation and purification of LRW of different physicochemical

  16. Characterization of electrochemically deposited films from aqueous and ionic liquid cobalt precursors toward hydrogen evolution reactions

    Energy Technology Data Exchange (ETDEWEB)

    Dushatinski, Thomas; Huff, Clay; Abdel-Fattah, Tarek M., E-mail: fattah@cnu.edu

    2016-11-01

    Highlights: • Co films deposition via aqueous and ionic liquid Precursors. • Hydrogen evolution produced from reactive surfaces. • Co deposited films characterized by SEM, AFM, EDX and XRD techniques. - Abstract: Electrodepositions of cobalt films were achieved using an aqueous or an ethylene glycol based non-aqueous solution containing choline chloride (vitamin B4) with cobalt chloride hexahydrate precursor toward hydrogen evolution reactions from sodium borohydride (NaBH{sub 4}) as solid hydrogen feedstock (SHF). The resulting cobalt films had reflectivity at 550 nm of 2.2% for aqueously deposited films (ACoF) and 1.3% for non-aqueously deposited films (NCoF). Surface morphology studied by scanning electron microscopy showed a positive correlation between particle size and thickness. The film thicknesses were tunable between >100 μm and <300 μm for each film. The roughness (Ra) value measurements by Dektak surface profiling showed that the NCoF (Ra = 165 nm) was smoother than the ACoF (Ra = 418 nm). The NCoFs and ACoFs contained only α phase (FCC) crystallites. The NCoFs were crystalline while the ACoFs were largely amorphous from X-ray diffraction analysis. The NCoF had an average Vickers hardness value of 84 MPa as compared to 176 MPa for ACoF. The aqueous precursor has a single absorption maximum at 510 nm and the non-aqueous precursor had three absorption maxima at 630, 670, and 695 nm. The hydrogen evolution reactions over a 1 cm{sup 2} catalytic surface with aqueous NaBH{sub 4} solutions generated rate constants (K) = equal to 4.9 × 10{sup −3} min{sup −1}, 4.6 × 10{sup −3} min{sup −1}, and 3.3 × 10{sup −3} min{sup −1} for ACoF, NCoF, and copper substrate respectively.

  17. Optimization and Application of Liquid Chromatography Determination of Dispersive Liquid-liquid Microextraction Purified Astaxanthin in Shrimp Waste

    Institute of Scientific and Technical Information of China (English)

    ZHU Tao; ROW Kyung-ho

    2013-01-01

    A new molecularly imprinted solid-phase extraction(MISPE) monolithic cartridge was synthesized,and MISPE-DLLME(DLLME=dispersive liquid-liquid microextraction) was developed for purification of astaxanthin in shrimp waste.The eluent(methanol) from MISPE was used as the dispersive solvent in subsequent DLLME for further purifying and enriching the analyte prior to high-performance liquid chromatography(HPLC) analysis.The mobile phase was methanol-acetonitrile-water-dichloromethane(85:5:5:5,volume ratio),flow rate was 0.7 mL/min and UV wavelength was 476 nm.Under optimal conditions,good linearity was obtained in a range of 0.2-200.0 μg/mL(r2=0.9998) with a limit of detection(LOD) of 0.08 μg/mL,and the extraction recoveries at three spiked levels ranged from 88.3%-92.5% with a relative standard deviation(RSD) less than 4.3%.Moreover,the mean contents of astaxanthin in the three batches of shrimp waste were 95.9,85.4 and 77.2 μg/g,respectively.This method combining the advantages of MISPE and DLLME results in high selectivity and low cost,which was applied to determining the astaxanthin level in shrimp waste samples.

  18. Removal of arsenate and arsenite from aqueous solution by waste cast iron.

    Science.gov (United States)

    Choi, Nag-Choul; Kim, Song-Bae; Kim, Soon-Oh; Lee, Jae-Won; Park, Jun-Boum

    2012-01-01

    The removal of As(III) and As(V) from aqueous solution was investigated using waste cast iron, which is a byproduct of the iron casting process in foundries. Two types of waste cast iron were used in the experiment: grind precipitate dust (GPD) and cast iron shot (CIS). The X-ray diffraction analysis indicated the presence of Feo on GPD and CIS. Batch experiments were performed under different concentrations of As(III) and As(V) and at various initial pH levels. Results showed that waste cast iron was effective in the removal of arsenic. The adsorption isotherm study indicated that the Langmuir isotherm was better than the Freundlich isotherm at describing the experimental result. In the adsorption of both As(IH) and As(V), the adsorption capacity of GPD was greater than CIS, mainly due to the fact that GPD had higher surface area and weight percent of Fe than CIS. Results also indicated the removal of As(III) and As(V) by GPD and CIS was influenced by the initial solution pH, generally decreasing with increasing pH from 3.0 to 10.5. In addition, both GPD and CIS were more effective at the removal of As(III) than As(V) under given experimental conditions. This study demonstrates that waste cast iron has potential as a reactive material to treat wastewater and groundwater containing arsenic.

  19. Extraction of copper(II) ions from aqueous solutions with a methimazole-based ionic liquid.

    Science.gov (United States)

    Reyna-González, Juan M; Torriero, Angel A J; Siriwardana, Amal I; Burgar, Iko M; Bond, Alan M

    2010-09-15

    The recently synthesized ionic liquid (IL) 2-butylthiolonium bis(trifluoromethanesulfonyl)amide, [mimSBu][NTf(2)], has been used for the extraction of copper(II) from aqueous solution. The pH of the aqueous phase decreases upon addition of [mimSBu](+), which is attributed to partial release of the hydrogen attached to the N(3) nitrogen atom of the imidazolium ring. The presence of sparingly soluble water in [mimSBu][NTf(2)] also is required in solvent extraction studies to promote the incorporation of Cu(II) into the [mimSBu][NTf(2)] ionic liquid phase. The labile copper(II) system formed by interacting with both the water and the IL cation component has been characterized by cyclic voltammetry as well as UV-vis, Raman, and (1)H, (13)C, and (15)N NMR spectroscopies. The extraction process does not require the addition of a complexing agent or pH control of the aqueous phase. [mimSBu][NTf(2)] can be recovered from the labile copper-water-IL interacting system by washing with a strong acid. High selectivity of copper(II) extraction is achieved relative to that of other divalent cobalt(II), iron(II), and nickel(II) transition-metal cations. The course of microextraction of Cu(2+) from aqueous media into the [mimSBu][NTf(2)] IL phase was monitored in situ by cyclic voltammetry using a well-defined process in which specific interaction with copper is believed to switch from the ionic liquid cation component, [mimSBu], to the [NTf(2)] anion during the course of electrochemical reduction from Cu(II) to Cu(I). The microextraction-voltammetry technique provides a fast and convenient method to determine whether an IL is able to extract electroactive metal ions from an aqueous solution.

  20. Solubilization of benzene, toluene, and xylene (BTX) in aqueous micellar solutions of amphiphilic imidazolium ionic liquids.

    Science.gov (United States)

    Łuczak, Justyna; Jungnickel, Christian; Markiewicz, Marta; Hupka, Jan

    2013-05-09

    Water-soluble ionic liquids may be considered analogues to cationic surfactants with a corresponding surface activity and ability to create organized structures in aqueous solutions. For the first time, the enhanced solubility of the aromatic hydrocarbons, benzene, toluene, and xylene, in aqueous micellar systems of 1-alkyl-3-methylimidazolium chlorides was investigated. Above a critical micelle concentration, a gradual increase in the concentration of aromatic hydrocarbons in the miceller solution was observed. This phenomenon was followed by means of the molar solubilization ratio, the micellar/water partition coefficient, and the number of solubilizate molecules per IL micelle. The molar solubilization ratio for ionic liquid micelles was found to be significantly higher when compared to that of ionic surfactants of similar chain length. The incorporation of the hydrocarbon into the micelle affects also an increase of the aggregation number.

  1. Probing Ionic Liquid Aqueous Solutions Using Temperature of Maximum Density Isotope Effects

    Directory of Open Access Journals (Sweden)

    Mohammad Tariq

    2013-03-01

    Full Text Available This work is a new development of an extensive research program that is investigating for the first time shifts in the temperature of maximum density (TMD of aqueous solutions caused by ionic liquid solutes. In the present case we have compared the shifts caused by three ionic liquid solutes with a common cation—1-ethyl-3-methylimidazolium coupled with acetate, ethylsulfate and tetracyanoborate anions—in normal and deuterated water solutions. The observed differences are discussed in terms of the nature of the corresponding anion-water interactions.

  2. Marangoni effect of cracked liquid film of an aqueous electrolyte flowing over a vertical heated plate

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    An experimental investigation was performed on Marangoni effect of cracked liquid film of aqueous Na2SO4 flowing over a vertical heated plate by using a sensitive infrared imaging technique. The results show that the thermal and solutal Marangoni effects, which result from the non-uniform distributions of surface temperature and concentration of the film, respectively, occur in the streamwise and transverse directions of the film, generating different influences on the film heat transfer. Taking account of the Marangoni number (Ma) and the solution concentration (c0), a correlation of the Nusselt number (Nu) for the cracked liquid film is proposed.

  3. Liquid Phase Micro-Extraction of Linear Alkylbenzene Sulfonate Anionic Surfactants in Aqueous Samples

    OpenAIRE

    2011-01-01

    Hollow fiber liquid phase micro-extraction (LPME) of linear alkylbenzene sulfonates (LAS) from aqueous samples was studied. Ion pair extraction of C10, C11, C12 and C13 homologues was facilitated with trihexylamine as ion-pairing agent, using di-n-hexylether as solvent for the supported liquid membrane (SLM). Effects of extraction time, acceptor buffer concentration, stirring speed, sample volume, NaCl and humic acids were studied. At 10–50 μg L−1 linear R2-coefficients were 0.99 for C10 and ...

  4. Shifts in the temperature of maximum density (TMD) of ionic liquid aqueous solutions.

    Science.gov (United States)

    Tariq, M; Esperança, J M S S; Soromenho, M R C; Rebelo, L P N; Lopes, J N Canongia

    2013-07-14

    This work investigates for the first time shifts in the temperature of maximum density (TMD) of water caused by ionic liquid solutes. A vast amount of high-precision volumetric data--more than 6000 equilibrated (static) high-precision density determination corresponding to ∼90 distinct ionic liquid aqueous solutions of 28 different types of ionic liquid--allowed us to analyze the TMD shifts for different homologous series or similar sets of ionic solutes and explain the overall effects in terms of hydrophobic, electrostatic and hydrogen-bonding contributions. The differences between the observed TMD shifts in the -2 temperatures are discussed taking into account the different types of possible solute-water interactions that can modify the structure of the aqueous phase. The results also reveal different insights concerning the nature of the ions that constitute typical ionic liquids and are consistent with previous results that established hydrophobic and hydrophilic scales for ionic liquid ions based on their specific interactions with water and other probe molecules.

  5. Cellulose/Gold Nanocrystal Hybrids via an Ionic Liquid/Aqueous Precipitation Route

    Directory of Open Access Journals (Sweden)

    Andreas Taubert

    2009-11-01

    Full Text Available Injection of a mixture of HAuCl4 and cellulose dissolved in the ionic liquid (IL 1-butyl-3-methylimidazolium chloride [Bmim]Cl into aqueous NaBH4 leads to colloidal gold nanoparticle/cellulose hybrid precipitates. This process is a model example for a very simple and generic approach towards (noble metal/cellulose hybrids, which could find applications in sensing, sterile filtration, or as biomaterials.

  6. Waste Tank Organic Safety Project: Analysis of liquid samples from Hanford waste tank 241-C-103

    Energy Technology Data Exchange (ETDEWEB)

    Pool, K.H.; Bean, R.M.

    1994-03-01

    A suite of physical and chemical analyses has been performed in support of activities directed toward the resolution of an Unreviewed Safety Question concerning the potential for a floating organic layer in Hanford waste tank 241-C-103 to sustain a pool fire. The analysis program was the result of a Data Quality Objectives exercise conducted jointly with staff from Westinghouse Hanford Company and Pacific Northwest Laboratory (PNL). The organic layer has been analyzed for flash point, organic composition including volatile organics, inorganic anions and cations, radionuclides, and other physical and chemical parameters needed for a safety assessment leading to the resolution of the Unreviewed Safety Question. The aqueous layer underlying the floating organic material was also analyzed for inorganic, organic, and radionuclide composition, as well as other physical and chemical properties. This work was conducted to PNL Quality Assurance impact level III standards (Good Laboratory Practices).

  7. Decontamination of liquid radioactive waste by thorium phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Rousselle, J.; Grandjean, S.; Dacheux, N.; Genet, M

    2004-07-01

    In the field of the complete reexamination of the chemistry of thorium phosphate and of the improvement of the homogeneity of Thorium Phosphate Diphosphate (TPD, Th{sub 4}(PO{sub 4}){sub 4}P{sub 2}O{sub 7}) prepared at high temperature, several crystallized compounds were prepared as initial powdered precursors. Due to the very low solubility products associated to these phases, their use in the field of the efficient decontamination of high-level radioactive liquid waste containing actinides (An) was carefully considered. Two main processes (called 'oxalate' and 'hydrothermal' chemical routes) were developed through a new concept combining the decontamination of liquid waste and the immobilization of the actinides in a ceramic matrix (TPD). In phosphoric media ('hydrothermal route'), the key-precursor was the Thorium Phosphate Hydrogen Phosphate hydrate (Th{sub 2}(PO{sub 4}){sub 2}(HPO{sub 4}). H{sub 2}O, TPHP, solubility product log(K{sub S,0}{sup 0}) {approx} - 67). The replacement of thorium by other tetravalent actinides (U, Np, Pu) in the structure, leading to the preparation of Th{sub 2-x/2}An{sub x/2}(PO{sub 4}){sub 2}(HPO{sub 4}). H{sub 2}O solid solutions, was examined. A second method was also considered in parallel to illustrate this concept using the more well-known precipitation of oxalate as the initial decontamination step. For this method, the final transformation to single phase TPD containing actinides was purchased by heating a mixture of phosphate ions with the oxalate precipitate at high temperature. (authors)

  8. Cloud Point and Liquid-Liquid Equilibrium Behavior of Thermosensitive Polymer L61 and Salt Aqueous Two-Phase System.

    Science.gov (United States)

    Rao, Wenwei; Wang, Yun; Han, Juan; Wang, Lei; Chen, Tong; Liu, Yan; Ni, Liang

    2015-06-25

    The cloud point of thermosensitive triblock polymer L61, poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO), was determined in the presence of various electrolytes (K2HPO4, (NH4)3C6H5O7, and K3C6H5O7). The cloud point of L61 was lowered by the addition of electrolytes, and the cloud point of L61 decreased linearly with increasing electrolyte concentration. The efficacy of electrolytes on reducing cloud point followed the order: K3C6H5O7 > (NH4)3C6H5O7 > K2HPO4. With the increase in salt concentration, aqueous two-phase systems exhibited a phase inversion. In addition, increasing the temperature reduced the concentration of salt needed that could promote phase inversion. The phase diagrams and liquid-liquid equilibrium data of the L61-K2HPO4/(NH4)3C6H5O7/K3C6H5O7 aqueous two-phase systems (before the phase inversion but also after phase inversion) were determined at T = (25, 30, and 35) °C. Phase diagrams of aqueous two-phase systems were fitted to a four-parameter empirical nonlinear expression. Moreover, the slopes of the tie-lines and the area of two-phase region in the diagram have a tendency to rise with increasing temperature. The capacity of different salts to induce aqueous two-phase system formation was the same order as the ability of salts to reduce the cloud point.

  9. Review of Potential Candidate Stabilization Technologies for Liquid and Solid Secondary Waste Streams

    Energy Technology Data Exchange (ETDEWEB)

    Pierce, Eric M.; Mattigod, Shas V.; Westsik, Joseph H.; Serne, R. Jeffrey; Icenhower, Jonathan P.; Scheele, Randall D.; Um, Wooyong; Qafoku, Nikolla

    2010-01-30

    Pacific Northwest National Laboratory has initiated a waste form testing program to support the long-term durability evaluation of a waste form for secondary wastes generated from the treatment and immobilization of Hanford radioactive tank wastes. The purpose of the work discussed in this report is to identify candidate stabilization technologies and getters that have the potential to successfully treat the secondary waste stream liquid effluent, mainly from off-gas scrubbers and spent solids, produced by the Hanford Tank Waste Treatment and Immobilization Plant (WTP). Down-selection to the most promising stabilization processes/waste forms is needed to support the design of a solidification treatment unit (STU) to be added to the Effluent Treatment Facility (ETF). To support key decision processes, an initial screening of the secondary liquid waste forms must be completed by February 2010.

  10. Using Surfer 8® to Interpret Light Non-Aqueous Phase Liquid Monitoring Data: A Case Study

    OpenAIRE

    Biesterveld, Andrew C.; Schneiter, R. Wane; Marsh, Raymond W.

    2004-01-01

    Remediation of aviation fuel present in the subsurface as light non-aqueous phase liquid (LNAPL) occurred from 1982 to 1996 at a facility in an industrial section of a small city in eastern Asia. An undetermined amount of the aviation fuel had leaked from underground storage tanks into the unconfined aquifer for an unknown, but extended, period. The release was discovered in 1981, and 57 monitoring wells were eventually constructed, along with a non-aqueous phase liquid r...

  11. Value added liquid products from waste biomass pyrolysis using pretreatments.

    Science.gov (United States)

    Das, Oisik; Sarmah, Ajit K

    2015-12-15

    Douglas fir wood, a forestry waste, was attempted to be converted into value added products by pretreatments followed by pyrolysis. Four different types of pretreatments were employed, namely, hot water treatment, torrefaction, sulphuric acid and ammonium phosphate doping. Subsequently, pyrolysis was done at 500°C and the resulting bio-oils were analysed for their chemical composition using Karl Fischer titration, thermogravimetry, ion exchange, and gas chromatography. Pretreatment with acid resulted in the highest yield of bio-oil (~60%). The acid and salt pretreatments were responsible for drastic reduction in the lignin oligomers and enhancement of water content in the pyrolytic liquid. The quantity of xylose/mannose reduced as a result of pretreatments. Although, the content of fermentable sugars remained similar across all the pretreatments, the yield of levoglucosan increased. Pretreatment of the biomass with acid yielded the highest amount of levoglucosan in the bio-oil (13.21%). The acid and salt pretreatments also elevated the amount of acetic acid in the bio-oils. Addition of acid and salt to the biomass altered the interaction of cellulose-lignin in the pyrolysis regime. Application of pretreatments should be based on the intended end use of the liquid product having a desired chemical composition.

  12. Electrochemical treatment of 2,4-dinitrophenol aqueous wastes using boron-doped diamond anodes

    Energy Technology Data Exchange (ETDEWEB)

    Canizares, P. [Department of Chemical Engineering, Facultad de Ciencias Quimicas, Universidad de Castilla-La Mancha, Campus Universitario s/n, 13071 Ciudad Real (Spain); Saez, C. [Department of Chemical Engineering, Facultad de Ciencias Quimicas, Universidad de Castilla-La Mancha, Campus Universitario s/n, 13071 Ciudad Real (Spain); Lobato, J. [Department of Chemical Engineering, Facultad de Ciencias Quimicas, Universidad de Castilla-La Mancha, Campus Universitario s/n, 13071 Ciudad Real (Spain); Rodrigo, M.A. [Department of Chemical Engineering, Facultad de Ciencias Quimicas, Universidad de Castilla-La Mancha, Campus Universitario s/n, 13071 Ciudad Real (Spain)]. E-mail: manuel.rodrigo@uclm.es

    2004-10-15

    The electrochemical oxidation of 2,4-dinitrophenol (2,4-DNP) aqueous wastes has been studied using both, bulk electrolysis and voltammetric techniques. To carry out the bulk electrolysis, a bench-scale plant with a single compartment electrochemical flow cell was used. Boron-doped diamond (BDD) materials were used as the anode and stainless steel (AISI 304) as the cathode. According to the obtained results, a simple mechanistic model has been proposed. The oxidation of 2,4-DNP leads to the appearance of phenol and quinonic compounds and to the release of the nitro groups from the aromatic ring, in a first step. In a second step, these organics are transformed into carboxylic acids (mainly maleic and oxalic acid). The process ends with the formation of carbon dioxide (CO{sub 2}). The effects of the waste characteristics (composition and pH) and of the operation parameters of the process (temperature and current density) have also been studied in this work. The complete removal of the organic compounds contained in the waste has been obtained in all essays.

  13. The Effect of Liquid Crystalline Structures on Antiseizure Properties of Aqueous Solutions of Ethoxylated Alcohols

    Directory of Open Access Journals (Sweden)

    Anna Bak

    2010-01-01

    Full Text Available Aqueous solutions of ethoxylated alcohols which form lyotropic liquid crystals at high concentrations (40–80% were selected as model lubricating substances. Microscopic studies under polarized light and viscosity measurements were carried out in order to confirm the presence of liquid crystalline structures in the case of alcohol solutions with ethoxylation degrees of 3, 5, 7 and 10. Microscopic images and viscosity coefficient values characteristic of various mesophases were obtained. As expected, the viscosity of LLCs decreases considerably with an increase in shearing rate which is characteristic of liquid crystals being non-Newtonian liquids. Antiseizure properties were determined by means of a four-ball machine (T-02 Tester and characterized by scuffing load (Pt, seizure load (Poz and limiting pressure of seizure (poz. Alcohol ethoxylates forming mesophases in aqueous solutions have the strongest effect on the Pt values which are several times higher than those measured in the presence of water. Ethoxylates with higher degrees of ethoxylation exhibit higher values of scuffing load. Those changes have been interpreted as a result of higher cloud points at which those compounds lose their amphiphilic properties. In general, the presence of mesophases in the bulk phase and particularly in the surface phase may lead to the formation of a lubricant film which separates the frictionally cooperating elements of a friction pair. The antiseizure efficiency of alcohol solutions is highest up to the load value which does not exceed the scuffing load value.

  14. The effect of liquid crystalline structures on antiseizure properties of aqueous solutions of ethoxylated alcohols.

    Science.gov (United States)

    Sulek, Marian Wlodzimierz; Bak, Anna

    2010-01-12

    Aqueous solutions of ethoxylated alcohols which form lyotropic liquid crystals at high concentrations (40-80%) were selected as model lubricating substances. Microscopic studies under polarized light and viscosity measurements were carried out in order to confirm the presence of liquid crystalline structures in the case of alcohol solutions with ethoxylation degrees of 3, 5, 7 and 10. Microscopic images and viscosity coefficient values characteristic of various mesophases were obtained. As expected, the viscosity of LLCs decreases considerably with an increase in shearing rate which is characteristic of liquid crystals being non-Newtonian liquids. Antiseizure properties were determined by means of a four-ball machine (T-02 Tester) and characterized by scuffing load (P(t)), seizure load (P(oz)) and limiting pressure of seizure (p(oz)). Alcohol ethoxylates forming mesophases in aqueous solutions have the strongest effect on the P(t) values which are several times higher than those measured in the presence of water. Ethoxylates with higher degrees of ethoxylation exhibit higher values of scuffing load. Those changes have been interpreted as a result of higher cloud points at which those compounds lose their amphiphilic properties. In general, the presence of mesophases in the bulk phase and particularly in the surface phase may lead to the formation of a lubricant film which separates the frictionally cooperating elements of a friction pair. The antiseizure efficiency of alcohol solutions is highest up to the load value which does not exceed the scuffing load value.

  15. Recovery of valuable materials from waste liquid crystal display panel.

    Science.gov (United States)

    Li, Jinhui; Gao, Song; Duan, Huabo; Liu, Lili

    2009-07-01

    Associated with the rapid development of the information and electronic industry, liquid crystal displays (LCDs) have been increasingly sold as displays. However, during the discarding at their end-of-life stage, significant environmental hazards, impacts on health and a loss of resources may occur, if the scraps are not managed in an appropriate way. In order to improve the efficiency of the recovery of valuable materials from waste LCDs panel in an environmentally sound manner, this study presents a combined recycling technology process on the basis of manual dismantling and chemical treatment of LCDs. Three key processes of this technology have been studied, including the separation of LCD polarizing film by thermal shock method the removal of liquid crystals between the glass substrates by the ultrasonic cleaning, and the recovery of indium metal from glass by dissolution. The results show that valuable materials (e.g. indium) and harmful substances (e.g. liquid crystals) could be efficiently recovered or separated through above-mentioned combined technology. The optimal conditions are: (1) the peak temperature of thermal shock to separate polarizing film, ranges from 230 to 240 degrees C, where pyrolysis could be avoided; (2) the ultrasonic-assisted cleaning was most efficient at a frequency of 40 KHz (P = 40 W) and the exposure of the substrate to industrial detergents for 10 min; and (3) indium separation from glass in a mix of concentrated hydrochloric acid at 38% and nitric acid at 69% (HCl:HNO(3):H(2)O = 45:5:50, volume ratio). The indium separation process was conducted with an exposure time of 30 min at a constant temperature of 60 degrees C.

  16. (Liquid + liquid) equilibria in ternary aqueous mixtures of phosphoric acid with organic solvents at T = 298.2 K

    Energy Technology Data Exchange (ETDEWEB)

    Ghanadzadeh, H., E-mail: hggilani@guilan.ac.i [Department of Chemistry, Faculty of Science, University of Guilan, Rasht (Iran, Islamic Republic of); Department of Chemical Engineering, University of Guilan, Rasht (Iran, Islamic Republic of); Ghanadzadeh, A., E-mail: aggilani@guilan.ac.i [Department of Chemistry, Faculty of Science, University of Guilan, Rasht (Iran, Islamic Republic of); Aghajani, Z.; Abbasnejad, S.; Shekarsaraee, S. [Department of Chemistry, Faculty of Science, University of Guilan, Rasht (Iran, Islamic Republic of)

    2010-06-15

    (Liquid + liquid) equilibrium (LLE) data for the ternary mixtures of left bracewater (1) + phosphoric acid (2) + organic solvents (3)right brace were determined at T = 298.2 K and atmospheric pressure. The organic solvents were cyclohexane, 2-methyl-2-butanol (tert-amyl alcohol), and isobutyl acetate. All the investigated systems exhibit Type-1 behaviour of LLE. The immiscibility region was found to be larger for the (water + phosphoric acid + cyclohexane) ternary system. The experimental LLE results were correlated with the NRTL model, and the binary interaction parameters were obtained. The reliability of the experimental tie-line results was tested through the Othmer-Tobias and Bachman correlation equations. Distribution coefficients and separation factors were evaluated over the immiscibility regions and a comparison of the extracting capabilities of the solvents was made with respect to these factors. The experimental results indicate the superiority of cyclohexane as the preferred solvent for the extraction of phosphoric acid from its aqueous solutions.

  17. Separation of curcuminoids using ionic liquid based aqueous two-phase system coupled with in situ dispersive liquid-liquid microextraction.

    Science.gov (United States)

    Shu, Yang; Gao, Mingcen; Wang, Xueying; Song, Rusheng; Lu, Jun; Chen, Xuwei

    2016-01-01

    An aqueous two-phase extraction system (ATPS) combined with an in situ dispersive liquid-liquid microextraction (DLLME) method using imidazolium ionic liquids (ILs) for the separation of curcuminoids is developed. The influence of structure of IL, the type of metathesis reagents, and the back extraction agents on the extraction efficiency is investigated. 2.0mg of curcuminoids are extracted by an IL ATPS composed of 0.4g 1,3-diethylimidazolium iodine (EeimI), 0.6g potassium hydrogen phosphate, 1.0g water. Then the bis[(trifluoromethyl)sulfonyl]imide lithium (LiNTf2) aqueous solution is added to the EeimI-rich phase of the ATPS. The water-immiscible ionic liquids, 1,3-diethylimidazole bis[(trifluoromethyl)sulfonyl]imide (EeimNTf2), forms by the metathesis reaction. The in situ DLLME is triggered simultaneously and further purifies the curcuminoids. 92% of EeimI transforms into EeimNTf2 and thus the Eeim(+) cation is used for twice in this method. Finally, 0.1mol/L NaOH aqueous solution is used as the back extraction reagent. The curcuminoids precipitate is achieved with 93% of recovery when the aqueous solution is adjusted to pH 3.0. This ATPS-DLLME method is successfully applied to the separation of curcuminoids from Curcuma Longa (0.96±0.02% of extraction yield, a purity of >51% with respect to the total dry mass of the product).

  18. Ion spatial distributions at the liquid-vapor interface of aqueous potassium fluoride solutions.

    Science.gov (United States)

    Brown, Matthew A; D'Auria, Raffaella; Kuo, I-F William; Krisch, Maria J; Starr, David E; Bluhm, Hendrik; Tobias, Douglas J; Hemminger, John C

    2008-08-28

    X-Ray photoemission spectroscopy operating under ambient pressure conditions is used to probe ion distributions throughout the interfacial region of a free-flowing aqueous liquid micro-jet of 6 M potassium fluoride. Varying the energy of the ejected photoelectrons by carrying out experiments as a function of X-ray wavelength measures the composition of the aqueous-vapor interfacial region at various depths. The F(-) to K(+) atomic ratio is equal to unity throughout the interfacial region to a depth of 2 nm. The experimental ion profiles are compared with the results of a classical molecular dynamics simulation of a 6 M aqueous KF solution employing polarizable potentials. The experimental results are in qualitative agreement with the simulations when integrated over an exponentially decaying probe depth characteristic of an APPES experiment. First principles molecular dynamics simulations have been used to calculate the potential of mean force for moving a fluoride anion across the air-water interface. The results show that the fluoride anion is repelled from the interface, consistent with the depletion of F(-) at the interface revealed by the APPES experiment and polarizable force field-based molecular dynamics simulation. Together, the APPES and MD simulation data provide a detailed description of the aqueous-vapor interface of alkali fluoride systems. This work offers the first direct observation of the ion distribution at an aqueous potassium fluoride solution interface. The current experimental results are compared to those previously obtained for saturated solutions of KBr and KI to underscore the strong difference in surface propensity between soft/large and hard/small halide ions in aqueous solution.

  19. Removal of arsenate and arsenite from aqueous solution by waste cast iron

    Institute of Scientific and Technical Information of China (English)

    Nag-Choul Choi; Song-Bae Kim; Soon-Oh Kim; Jae-Won Lee; Jun-Boum Park

    2012-01-01

    The removal of As(Ⅲ) and As(Ⅴ) from aqueous solution was investigated using waste cast iron,which is a byproduct of the iron casting process in foundries.Two types of waste cast iron were used in the experiment:grind precipitate dust (GPD) and cast iron shot (CIS).The X-ray diffraction analysis indicated the presence of Fe0 on GPD and CIS.Batch experiments were performed under different concentrations of As(Ⅲ) and As(Ⅴ) and at various initial pH levels.Results showed that waste cast iron was effective in the removal of arsenic.The adsorption isotherm study indicated that the Langmuir isotherm was better than the Freundlich isotherm at describing the experimental result.In the adsorption of both As(Ⅲ) and As(Ⅴ),the adsorption capacity of GPD was greater than CIS,mainly due to the fact that GPD had higher surface area and weight percent of Fe than CIS.Results also indicated the removal of As(Ⅲ) and As(Ⅴ)by GPD and CIS was influenced by the initial solution pH,generally decreasing with increasing pH from 3.0 to 10.5.In addition,both GPD and CIS were more effective at the removal of As(Ⅲ) than As(Ⅴ) under given experimental conditions.This study demonstrates that waste cast iron has potential as a reactive material to treat wastewater and groundwater containing arsenic.

  20. ICPP radioactive liquid and calcine waste technologies evaluation final report and recommendation

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-04-01

    Using a formalized Systems Engineering approach, the Latched Idaho Technologies Company developed and evaluated numerous alternatives for treating, immobilizing, and disposing of radioactive liquid and calcine wastes at the Idaho Chemical Processing Plant. Based on technical analysis data as of March, 1995, it is recommended that the Department of Energy consider a phased processing approach -- utilizing Radionuclide Partitioning for radioactive liquid and calcine waste treatment, FUETAP Grout for low-activity waste immobilization, and Glass (Vitrification) for high-activity waste immobilization -- as the preferred treatment and immobilization alternative.

  1. Selective separation of protein and saccharides by ionic liquids aqueous two-phase systems

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    In the present work,it was found that aqueous solution of a hydrophilic ionic liquid (IL),1-butyl-3-methylimidazolium dicyanamide ([C4mim][N(CN)2]),could be separated into an aqueous two-phase system (ATPS) by inorganic salts such as K2HPO4 and K3PO4.The top phase is IL-rich,while the bottom phase is phosphate-rich.It was shown that 82.7%-100% bovine serum albumin (BSA) could be enriched into the top phase and almost quantitative saccharides (arabinose,glucose,sucrose,raffinose or dextran) were preferentially extracted into the bottom phase in a single-step extraction by [C4mim][N(CN)2] + K2HPO4 ATPS.The extraction efficiency of BSA from the aqueous saccharide solutions was influenced by the molecular structure of saccharides.The conductivity,dynamic light scattering (DLS) and transmission electron microscopy (TEM) were combined to investigate the microstructure of the IL-rich top phase and the possible mechanism for the selective separation.It is suggested that the formation of the IL aggregate and the IL aggregate-BSA complex plays a significant role in the separation of BSA from aqueous saccharide solutions.This is the first example for the selective separation by ILs-based ATPSs.It is expected that these findings would have potential applications in bio-analysis,separation,and IL recycle.

  2. A Regulatory Analysis and Reassessment of U.S. Environmental Protection Agency Listed Hazardous Waste Numbers for Applicability to the INTEC Liquid Waste System

    Energy Technology Data Exchange (ETDEWEB)

    Gilbert, K.L.; Venneman, T.E.

    1998-12-01

    This report concludes that there are four listed hazardous waste numbers (F001, F002, F005, and U134) applicable to the waste in the Process Equipment Waste Evaporator (PEWE) liquid waste system at the Idaho National Engineering and Environmental Laboratory. The chemical constituents associated with these listed hazardous waste numbers, including those listed only for ignitability are identified. The RCRA Part A permit application hazardous waste numbers identify chemical constituents that may be treated or stored by the PEWE liquid waste system either as a result of a particular characteristic (40 CFR, Subpart C) or as a result of a specific process (40 CFR 261, Subpart D). The RCRA Part A permit application for the PEWE liquid waste system identifies the universe of Environmental Protection Agency (EPA) hazardous waste numbers [23 characteristic (hazardous waste codes) numbers and 105 listed numbers (four F-listed hazardous waste numbers, 20 P-listed hazardous waste numbers, and 81 U-listed hazardous waste numbers)] deemed acceptable for storage and treatment. This evaluation, however, identifies only listed wastes (and their chemical constituents) that have actually entered the PEWE liquid waste system and would, therefore, be assigned to the PEWE liquids and treatment residuals.

  3. Alkali treated Foumanat tea waste as an efficient adsorbent for methylene blue adsorption from aqueous solution

    Directory of Open Access Journals (Sweden)

    Azadeh Ebrahimian Pirbazari

    2014-08-01

    Full Text Available The adsorption of methylene blue (MB from aqueous solution by alkali treated Foumanat tea waste (ATFTW from agriculture biomass was investigated. The adsorbent was characterized by Scanning Electron Microscopy (SEM, Fourier Transform-Infrared Spectroscopy (FT-IR and nitrogen physisorption. FTIR results showed complexation and ion exchange appear to be the principle mechanism for MB adsorption. The adsorption isotherm data were fitted to Langmuir, Sips, Redlich-Peterson and Freundlich equations, and the Langmuir adsorption capacity, Qmax was found to be 461 mgg−1. It was found that the adsorption of MB increases by increasing temperature from 303 to 323 K and the process is endothermic in nature. The removal of MB by ATFTW followed pseudo-second order reaction kinetics based on Lagergren equations. Mechanism studies indicated that the adsorption of MB on the ATFTW was mainly governed by external mass transport where particle diffusion was the rate limiting step.

  4. Removal of Lead (II Ions from Aqueous Solutions onto Activated Carbon Derived from Waste Biomass

    Directory of Open Access Journals (Sweden)

    Murat Erdem

    2013-01-01

    Full Text Available The removal of lead (II ions from aqueous solutions was carried out using an activated carbon prepared from a waste biomass. The effects of various parameters such as pH, contact time, initial concentration of lead (II ions, and temperature on the adsorption process were investigated. Energy Dispersive X-Ray Spectroscopy (EDS analysis after adsorption reveals the accumulation of lead (II ions onto activated carbon. The Langmuir and Freundlich isotherm models were applied to analyze equilibrium data. The maximum monolayer adsorption capacity of activated carbon was found to be 476.2 mg g−1. The kinetic data were evaluated and the pseudo-second-order equation provided the best correlation. Thermodynamic parameters suggest that the adsorption process is endothermic and spontaneous.

  5. A Novel Agricultural Waste Adsorbent, Watermelon Shell for the Removal of Copper from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Koel Banerjee

    2012-01-01

    Full Text Available The present study deals with the application of Watermelon Shell, an agricultural waste, for the adsorptive removal of Cu(II from its aqueous solutions. This paper incorporates the effects of time, dose,temperature, concentration, particle size, agitation speed and pH. Analytical techniques have been employed to find pore properties and characteristics of adsorbent materials. Batch kinetic and isotherm studies have also been performed to understand the ability of the adsorbents. The adsorption behavior of the Cu(II has beenstudied using Freundlich, Langmuir and Tempkin adsorption isotherm models. The monolayer adsorption capacity determined from the Langmuir adsorption equation has been found as 111.1 mg/g. Kineticmeasurements suggest the involvement of pseudo-second-order kinetics in adsorptions and is controlled by a particle diffusion process. Adsorption of Cu(II on adsorbents was found to increase on decreasing initial concentration, increasing pH up to 8, increasing temperature, increasing agitation speed and decreasing particlesize. Overall, the present findings suggest that watermelon outer shell is environmentally friendly, efficient and low-cost biosorbent which is useful for the removal of Cu(II from aqueous media.

  6. Removal of lead(II) from aqueous solutions using carbonate hydroxyapatite extracted from eggshell waste.

    Science.gov (United States)

    Liao, Dexiang; Zheng, Wei; Li, Xiaoming; Yang, Qi; Yue, Xiu; Guo, Liang; Zeng, Guangming

    2010-05-15

    Carbonate hydroxyapatite (CHAP) synthesized from eggshell waste was used for removing lead ion from aqueous solutions. The effects of pH, contact time and initial concentration were studied in batch experiments. The maximum uptake of lead ion was obtained at pH 6.0. Adsorption equilibrium was established by 60 min. The pseudo-first order, pseudo-second order and intraparticle diffusion kinetic models were applied to study the kinetics of the sorption processes. The pseudo-second order kinetic model provided the best correlation (R(2)>0.9991) of the used experimental data compared to the pseudo-first order and intraparticle diffusion kinetic models. The adsorption of lead ion by CHAP increased as the initial concentration of lead ion increased in the medium. The maximum lead ion adsorbed was found to be 101 mg g(-1). It was found that the adsorption of Pb(II) on CHAP was correlated well (R(2)=0.9995) with the Langmuir equation as compared to Freundlich isotherm equation under the concentration range studied. This study indicated that CHAP could be used as an efficient adsorbent for removal of lead ion from aqueous solution.

  7. The Addition of Hatchery Liquid Waste to Dairy Manure Improves Anaerobic Digestion

    Directory of Open Access Journals (Sweden)

    WRT Lopes

    Full Text Available ABSTRACT The objective of this study was to determine the optimal inclusion level of liquid egg hatchery waste for the anaerobic co-digestion of dairy cattle manure. A completely randomized experimental was applied, with seven treatments (liquid hatchery waste to cattle manure ratios of0: 100, 5:95, 10:90, 15:85, 20:80, 25:75 and 30:70, with five replicates (batch digester model each. The evaluated variables were disappearance of total solids (TS, volatile solids (VS, and neutral detergent fiber (NDF, and specific production of biogas and of methane. Maximum TS and VS disappearance of 41.3% and 49.6%, were obtained at 15.5% and 16.0% liquid hatchery waste inclusion levels. The addition of 22.3% liquid hatchery considerably reduced NDF substrate content (53.2%. Maximum specific biogas production was obtained with 17% liquid hatchery waste, with the addition of 181.7 and 229.5 L kg-1TS and VS, respectively. The highest methane production, at 120.1 and 151.8 L CH4 kg-1TS and VS, was obtained with the inclusion of 17.5 and 18.0% liquid hatchery waste, respectively. The addition of liquid hatchery waste atratios of up to 15.5%in co-digestion with cattle manure reduced solid and fiber levels in the effluent, and improved biogas and methane production.

  8. Influence of liquid structure on diffusive isotope separation in molten silicates and aqueous solutions

    Science.gov (United States)

    Watkins, James M.; DePaolo, Donald J.; Ryerson, Frederick J.; Peterson, Brook T.

    2011-06-01

    Molecular diffusion in natural volcanic liquids discriminates between isotopes of major ions (e.g., Fe, Mg, Ca, and Li). Although isotope separation by diffusion is expected on theoretical grounds, the dependence on mass is highly variable for different elements and in different media. Silicate liquid diffusion experiments using simple liquid compositions were carried out to further probe the compositional dependence of diffusive isotopic discrimination and its relationship to liquid structure. Two diffusion couples consisting of the mineral constituents anorthite (CaAl 2Si 2O 8; denoted AN), albite (NaAlSi 3O 8; denoted AB), and diopside (CaMgSi 2O 6; denoted DI) were held at 1450 °C for 2 h and then quenched to ambient pressure and temperature. Major-element as well as Ca and Mg isotope profiles were measured on the recovered quenched glasses. In both experiments, Ca diffuses rapidly with respect to Si. In the AB-AN experiment, D Ca/ D Si ≈ 20 and the efficiency of isotope separation for Ca is much greater than in natural liquid experiments where D Ca/ D Si ≈ 1. In the AB-DI experiment, D Ca/ D Si ≈ 6 and the efficiency of isotope separation is between that of the natural liquid experiments and the AB-AN experiment. In the AB-DI experiment, D Mg/ D Si ≈ 1 and the efficiency of isotope separation for Mg is smaller than it is for Ca yet similar to that observed for Mg in natural liquids. The results from the experiments reported here, in combination with results from natural volcanic liquids, show clearly that the efficiency of diffusive separation of Ca isotopes is systematically related to the solvent-normalized diffusivity - the ratio of the diffusivity of the cation ( D Ca) to the diffusivity of silicon ( D Si). The results on Ca isotopes are consistent with available data on Fe, Li, and Mg isotopes in silicate liquids, when considered in terms of the parameter D cation/ D Si. Cations diffusing in aqueous solutions display a similar relationship

  9. Glass-to-cryogenic-liquid transitions in aqueous solutions suggested by crack healing.

    Science.gov (United States)

    Kim, Chae Un; Tate, Mark W; Gruner, Sol M

    2015-09-22

    Observation of theorized glass-to-liquid transitions between low-density amorphous (LDA) and high-density amorphous (HDA) water states had been stymied by rapid crystallization below the homogeneous water nucleation temperature (∼235 K at 0.1 MPa). We report optical and X-ray observations suggestive of glass-to-liquid transitions in these states. Crack healing, indicative of liquid, occurs when LDA ice transforms to cubic ice at 160 K, and when HDA ice transforms to the LDA state at temperatures as low as 120 K. X-ray diffraction study of the HDA to LDA transition clearly shows the characteristics of a first-order transition. Study of the glass-to-liquid transitions in nanoconfined aqueous solutions shows them to be independent of the solute concentrations, suggesting that they represent an intrinsic property of water. These findings support theories that LDA and HDA ice are thermodynamically distinct and that they are continuously connected to two different liquid states of water.

  10. Aqueous interfaces with hydrophobic room-temperature ionic liquids: a molecular dynamics study.

    Science.gov (United States)

    Chaumont, A; Schurhammer, R; Wipff, G

    2005-10-13

    We report a molecular dynamics study of the interface between water and (macroscopically) water-immiscible room-temperature ionic liquids "ILs", composed of PF6(-) anions and butyl- versus octyl-substituted methylimidazolium+ cations (noted BMI+ and OMI+). Because the parameters used to simulate the pure ILs were found to exaggerate the water/IL mixing, they have been modified by scaling down the atomic charges, leading to better agreement with the experiment. The comparison of [OMI][PF6] versus [BMI][PF6] ILs demonstrates the importance of the N-alkyl substituent on the extent of solvent mixing and on the nature of the interface. With the most hydrophobic [OMI][PF6] liquid, the "bulk" IL phase is dryer than with the [BMI][PF6] liquid. At the interface, the OMI+ cations retain direct contacts with the bulk IL, whereas the more hydrophilic PF6(-) anions gradually dilute in the local water micro-environment and are thus isolated from the "bulk" IL. The interfacial OMI+ cations are ordered with their imidazolium moiety pointing toward the aqueous side and their octyl chains toward the IL side of the interface. With the [BMI][PF6] liquid, the system gradually evolves from an IL-rich to a water-rich medium, leading to an ill-defined interfacial domain with high intersolvent mixing. As a result, the BMI+ cations are isotropically oriented "at the interface". Because the imidazolium cations are more hydrophobic than the PF6(-) anions, the charge distribution at the interface is heterogeneous, leading to a positive electrostatic potential at the interface with the two studied ILs. Mixing-demixing simulations on [BMI][PF6]/water mixtures are also reported, comparing Ewald versus reaction field treatments of electrostatics. Phase separation is very slow (at least 30 ns), in marked contrast with mixtures involving classical organic liquids, which separate in less than 0.5 ns at the microscopic level. The results allow us to better understand the specificity of the aqueous

  11. Adsorption of Cr(VI) and Pb(II) from aqueous solution using agricultural solid waste.

    Science.gov (United States)

    Geetha, A; Sivakumar, P; Sujatha, M; Palanisamy, P N

    2009-04-01

    Areca nut shell, an agricultural solid waste by-product, has been studied for the removal of heavy metals Cr(VI) and Pb(II) from aqueous solution. Parameters, such as equilibrium time, effect of initial metal ion concentration, effect of pH on the removal, were analyzed. An initial pH of 4.0 was found most favourable for Cr(VI) removal and 5.0 for Pb(II) removal. Two theoretical isotherm models, namely Langmuir and Freundlich, were analyzed for the applicability of the experimental data. The Langmuir adsorption capacity (Q0) was calculated. The results of thermodynamic parameters suggest the exothermic nature of the adsorption. The desorption studies were carried out using dilute hydrochloric acid. Maximum desorption of 88% for Cr(VI) and 91% for Pb(II) were achieved. Areca nut shell waste, the low cost adsorbent is found to be effective in the removal of Cr(VI) and Pb(II) ions, and hence it can be applied for the removal of heavy metals from industrial wastewater.

  12. Purification and characterization of polyphenol oxidase from waste potato peel by aqueous two-phase extraction.

    Science.gov (United States)

    Niphadkar, Sonali S; Vetal, Mangesh D; Rathod, Virendra K

    2015-01-01

    Potato peel from food industrial waste is a good source of polyphenol oxidase (PPO). This work illustrates the application of an aqueous two-phase system (ATPS) for the extraction and purification of PPO from potato peel. ATPS was composed of polyethylene glycol (PEG) and potassium phosphate buffer. Effect of different process parameters, namely, PEG, potassium phosphate buffer, NaCl concentration, and pH of the system, on partition coefficient, purification factor, and yield of PPO enzyme were evaluated. Response surface methodology (RSM) was utilized as a statistical tool for the optimization of ATPS. Optimized experimental conditions were found to be PEG1500 17.62% (w/w), potassium phosphate buffer 15.11% (w/w), and NaCl 2.08 mM at pH 7. At optimized condition, maximum partition coefficient, purification factor, and yield were found to be 3.7, 4.5, and 77.8%, respectively. After partial purification of PPO from ATPS, further purification was done by gel chromatography where its purity was increased up to 12.6-fold. The purified PPO enzyme was characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), followed by Km value 3.3 mM, and Vmax value 3333 U/mL, and enzyme stable ranges for temperature and pH of PPO were determined. These results revealed that ATPS would be an attractive option for obtaining purified PPO from waste potato peel.

  13. Removal of cadmium from aqueous solutions by adsorption onto orange waste

    Energy Technology Data Exchange (ETDEWEB)

    Perez-Marin, A.B. [Department of Chemical Engineering, University of Murcia, 30071 Murcia (Spain); Zapata, V. Meseguer [Department of Chemical Engineering, University of Murcia, 30071 Murcia (Spain)]. E-mail: vzapata@um.es; Ortuno, J.F. [Department of Chemical Engineering, University of Murcia, 30071 Murcia (Spain); Aguilar, M. [Department of Chemical Engineering, University of Murcia, 30071 Murcia (Spain); Saez, J. [Department of Chemical Engineering, University of Murcia, 30071 Murcia (Spain); Llorens, M. [Department of Chemical Engineering, University of Murcia, 30071 Murcia (Spain)

    2007-01-02

    The use of orange wastes, generated in the orange juice industry, for removing cadmium from aqueous solutions has been investigated. The material was characterized by Fourier transform infrared spectroscopy and batch experiments were conducted to determine the adsorption capacity of the biomass. A strong dependence of the adsorption capacity on pH was observed, the capacity increasing as pH value rose. Kinetics and adsorption equilibrium were studied at different pH values (4-6). The adsorption process was quick and the equilibrium was attained within 3 h. The maximum adsorption capacity of orange waste was found to be 0.40, 0.41 and 0.43 mmol/g at pH 4-6, respectively. The kinetic data were analysed using various kinetic models - pseudo-first order equation, pseudo-second order equation, Elovich equation and intraparticle diffusion equation - and the equilibrium data were tested using four isotherm models - Langmuir, Freundlich, Sips and Redlich-Peterson. The data were fitted by non-linear regression and five error analysis methods were used to evaluate the goodness of the fit. The Elovich equation provides the greatest accuracy for the kinetic data and the Sips model the closest fit for the equilibrium data.

  14. Evaluating Transport and Attenuation of Inorganic Contaminants in the Vadose Zone for Aqueous Waste Disposal Sites

    Energy Technology Data Exchange (ETDEWEB)

    Truex, Michael J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Oostrom, Martinus [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Tartakovsky, Guzel D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2015-09-01

    An approach was developed for evaluating vadose zone transport and attenuation of aqueous wastes containing inorganic (non-volatile) contaminants that were disposed of at the land surface (i.e., directly to the ground in cribs, trenches, tile fields, etc.) and their effect on the underlying groundwater. The approach provides a structured method for estimating transport of contaminants through the vadose zone and the resulting temporal profile of groundwater contaminant concentrations. The intent of the approach is also to provide a means for presenting and explaining the results of the transport analysis in the context of the site-specific waste disposal conditions and site properties, including heterogeneities and other complexities. The document includes considerations related to identifying appropriate monitoring to verify the estimated contaminant transport and associated predictions of groundwater contaminant concentrations. While primarily intended for evaluating contaminant transport under natural attenuation conditions, the approach can also be applied to identify types of, and targets for, mitigation approaches in the vadose zone that would reduce the temporal profile of contaminant concentrations in groundwater, if needed.

  15. Biogas production from the mechanically pretreated, liquid fraction of sorted organic municipal solid wastes.

    Science.gov (United States)

    Alvarado-Lassman, A; Méndez-Contreras, J M; Martínez-Sibaja, A; Rosas-Mendoza, E S; Vallejo-Cantú, N A

    2016-09-13

    The high liquid content in fruit and vegetable wastes makes it convenient to mechanically separate these wastes into mostly liquid and solid fractions by means of pretreatment. Then, the liquid fraction can be treated using a high-rate anaerobic biofilm reactor to produce biogas, simultaneously reducing the amount of solids that must be landfilled. In this work, the specific composition of municipal solid waste (MSW) in a public market was determined; then, the sorted organic fraction of municipal solid waste was treated mechanically to separate and characterize the mostly liquid and solid fractions. Then, the mesophilic anaerobic digestion for biogas production of the first fraction was evaluated. The anaerobic digestion resulted in a reduced hydraulic retention time of two days with high removal of chemical oxygen demand, that is, 88% on average, with the additional benefit of reducing the mass of the solids that had to be landfilled by about 80%.

  16. Mechanism of conversion of cellulosic wastes to liquid fuels in alkaline solution

    Energy Technology Data Exchange (ETDEWEB)

    Molton, P.M.; Demmitt, T.F.; Donovan, J.M.; Miller, R.K.

    1978-01-01

    Conversion of cellulosic wastes into liquid oils is being practiced on a pilot plant scale at Albany, OR, but the fundamental chemistry of the process is poorly understood. We report our findings on the aqueous alkaline digestion of pure cellulose, on a laboratory scale, in a closely related system. Our intent is to elucidate the reaction mechanisms involved in oil and tar formation, and to identify products of potential value. A 30 wt % aqueous slurry of pure cellulose in up to 1.2 N alkali (sodium hydroxide or carbonate), heated to 350/sup 0/C over a 3.5 hour period showed a sharp discontinuity in heating rate at 265 to 270/sup 0/C, indicating the onset of a discrete liquefaction reaction not hitherto observed. A series of 129 autoclave experiments analyzed by statistical methods indicated that carbon monoxide, while it promotes the attainment of high yields as claimed by the Bureau of Mines, is not necessary for the reaction to proceed. Analysis of the products by /sup 13/C-NMR, GC/MS, and gel permeation chromatography indicated that the nonvolatile fraction of the oil consists of 44% aromatic carbon and 7% aromatic hydrogen, corresponding to a benzenoid polyaromatic with a substitution ratio of 5:1. However, oxygen content of the nonvolatile fraction and distillable oil is approximately the same. Since the oil contains a series of polyalkylated furans, this suggests that the char is a poly-furan rather than a conventional asphaltene derivative. Volatile products from the oil fraction consist of furans, cyclic ketones, linear and branched alkenes, and phenolics. The high proportion of phenolics relative to normal crude oil could explain the observed highly corrosive nature of the biomass-derived oils.

  17. Vine-shoot waste aqueous extract applied as foliar fertilizer to grapevines: Effect on amino acids and fermentative volatile content.

    Science.gov (United States)

    Sánchez-Gómez, R; Garde-Cerdán, T; Zalacain, A; Garcia, R; Cabrita, M J; Salinas, M R

    2016-04-15

    The aim of this work was to study the influence of foliar applications of different wood aqueous extracts on the amino acid content of musts and wines from Airén variety; and to study their relationship with the volatile compounds formed during alcoholic fermentation. For this purpose, the foliar treatments proposed were a vine-shoot aqueous extract applied in one and two times, and an oak extract which was only applied once. Results obtained show the potential of Airén vine-shoot waste aqueous extracts to be used as foliar fertilizer, enhancing the wine amino acid content especially when they were applied once. Similar results were observed with the aqueous oak extract. Regarding wine fermentative volatile compounds, there is a close relationship between musts and their wines amino acid content allowing us to discuss about the role of proline during the alcoholic fermentation and the generation of certain volatiles.

  18. Stabilization of liquid low-level and mixed wastes: a treatability study

    Energy Technology Data Exchange (ETDEWEB)

    Carson, S.; Cheng, Yu-Cheng; Yellowhorse, L.; Peterson, P.

    1996-02-01

    A treatability study has been conducted on liquid low-level and mixed wastes using the stabilization agents Aquaset, Aquaset II, Aquaset II-H, Petroset, Petroset-H, and Petroset and Petroset II. A total of 40 different waste types with activities ranging from 10{sup {minus}14} to 10{sup {minus}4} curies/ml have been stabilized. Reported data for each waste include its chemical and radiological composition and the optimum composition or range of compositions (weight of agent/volume of waste) for each stabilization agent used. All wastes were successfully stabilized with one or more of the stabilization agents and all final waste forms passed the Paint Filter Liquids Test (EPA Method 9095).

  19. Evaluation of mercury in liquid waste processing facilities - Phase I report

    Energy Technology Data Exchange (ETDEWEB)

    Jain, V. [Savannah River Site (SRS), Aiken, SC (United States); Occhipinti, J. E. [Savannah River Site (SRS), Aiken, SC (United States); Shah, H. [Savannah River Site (SRS), Aiken, SC (United States); Wilmarth, W. R. [Savannah River Site (SRS), Aiken, SC (United States); Edwards, R. E. [Savannah River Site (SRS), Aiken, SC (United States)

    2015-07-01

    This report provides a summary of Phase I activities conducted to support an Integrated Evaluation of Mercury in Liquid Waste System (LWS) Processing Facilities. Phase I activities included a review and assessment of the liquid waste inventory and chemical processing behavior of mercury using a system by system review methodology approach. Gaps in understanding mercury behavior as well as action items from the structured reviews are being tracked. 64% of the gaps and actions have been resolved.

  20. Evaluation of Mercury in Liquid Waste Processing Facilities - Phase I Report

    Energy Technology Data Exchange (ETDEWEB)

    Jain, V. [Savannah River Site (SRS), Aiken, SC (United States); Occhipinti, J. [Savannah River Site (SRS), Aiken, SC (United States); Shah, H. [Savannah River Site (SRS), Aiken, SC (United States); Wilmarth, B. [Savannah River Site (SRS), Aiken, SC (United States); Edwards, R. [Savannah River Site (SRS), Aiken, SC (United States)

    2015-07-01

    This report provides a summary of Phase I activities conducted to support an Integrated Evaluation of Mercury in Liquid Waste System (LWS) Processing Facilities. Phase I activities included a review and assessment of the liquid waste inventory and chemical processing behavior of mercury using a system by system review methodology approach. Gaps in understanding mercury behavior as well as action items from the structured reviews are being tracked. 64% of the gaps and actions have been resolved.

  1. SOLID AND LIQUID PINEAPPLE WASTE UTILIZATION FOR LACTIC ACID FERMENTATION USING Lactobacillus delbrueckii

    OpenAIRE

    Abdullah Abdullah

    2012-01-01

    The liquid and solid  pineapple wastes contain mainly sucrose, glucose, fructose and other nutrients. It therefore can potentially be used as carbon source for fermentation to produce organic acid. Recently, lactic acid has been considered to be an important raw material for production of biodegradable lactate polymer. The experiments were  carried out in batch fermentation using  the  liquid and solid pineapple wastes to produce lactic acid. The anaerobic fermentation of ...

  2. Statistical optimization of aqueous extraction of pectin from waste durian rinds.

    Science.gov (United States)

    Maran, J Prakash

    2015-02-01

    The objectives of this present study was to investigate and optimize the aqueous extraction conditions such as solid-liquid (SL) ratio (1:5-1:15 g/ml), pH (2-3), extraction time (20-60 min) and extraction temperature (75-95 °C) on maximum extraction of pectin from durian rinds using four factors, three levels Box-Behnken response design. The experimental data obtained were fitted to a second-order polynomial equation using multiple regression analysis and analyzed by analysis of variance (ANOVA). The optimum extraction condition was found to be as follows: SL ratio of 1:10 g/ml, pH of 2.8, extraction time of 43 min and extraction temperature of 86 °C respectively. Under the optimal conditions, the experimental pectin yield (9.1%) was well correlated with predicted yield (9.3%).

  3. Influence of Temperature on Induction Period of Denitration During Concentration of Radioactive Acid Liquid Waste

    Institute of Scientific and Technical Information of China (English)

    YANG; Hui; LI; Chuan-bo; YAN; Tai-hong; ZHENG; Wei-fang

    2013-01-01

    To minimize the volume of waste and recycle nitric acid,the high-and middle-level radioactive liquid waste from reprocessing plant need to be concentrated and de-nitrated,and formic acid and formaldehyde are widely applied as denitration agents.Temperature can affect the induction period of denitration reaction and the safety of process.

  4. EFFECT OF LIQUID TO SOLID RATIO ON LEACHING OF METALS FROM MINERAL PROCESSING WASTE

    Science.gov (United States)

    Various anthropogenic activities generate hazardous solid wastes that are affluent in heavy metals, which can cause significant damage to the environment an human health. A mineral processing waste was used to study the effect of liquid to solid ratio (L/S) on the leaching behav...

  5. Liquid-liquid equilibrium of water + PEG 8000 + magnesium sulfate or sodium sulfate aqueous two-phase systems at 35°C: experimental determination and thermodynamic modeling

    Directory of Open Access Journals (Sweden)

    B. D. Castro

    2005-09-01

    Full Text Available Liquid-liquid extraction using aqueous two-phase systems is a highly efficient technique for separation and purification of biomolecules due to the mild properties of both liquid phases. Reliable data on the phase behavior of these systems are essential for the design and operation of new separation processes; several authors reported phase diagrams for polymer-polymer systems, but data on polymer-salt systems are still relatively scarce. In this work, experimental liquid-liquid equilibrium data on water + polyethylene glycol 8000 + magnesium sulfate and water + polyethylene glycol 8000 + sodium sulfate aqueous two-phase systems were obtained at 35°C. Both equilibrium phases were analyzed by lyophilization and ashing. Experimental results were correlated with a mass-fraction-based NRTL activity coefficient model. New interaction parameters were estimated with the Simplex method. The mean deviations between the experimental and calculated compositions in both equilibrium phases is about 2%.

  6. Determination of mitomycin C in human aqueous humor and serum by high-performance liquid chromatography.

    Science.gov (United States)

    Li, W Y; Seah, S K; Koda, R T

    1993-09-08

    Mitomycin C (MMC) is used in the treatment of disseminated adenocarcinoma of the stomach and pancreas and is used in ophthalmology as adjunctive therapy in trabeculectomy. Since only small volumes of aqueous humor are available for analysis, a sensitive method requiring limited sample preparation was developed. An internal standard, 4-aminoacetophenone, was added to aqueous humor specimens, and the solution was directly injected into the high-performance liquid chromatographic (HPLC) column. The use of a short 50-mm C18 reversed-phase column gave adequate resolution of peaks with improved sensitivity. The method was applicable for determination of MMC in serum, although solid-phase extraction for sample clean-up was required prior to injection into the HPLC column, and analytical columns of 150-250 mm were necessary for adequate resolution of peaks. The method has been validated and is linear from 6.25 to 50 ng/ml in aqueous humor and from 10 to 500 ng/ml in serum.

  7. Dispersive Liquid-Liquid Microextraction Combined with Ultrahigh Performance Liquid Chromatography/Tandem Mass Spectrometry for Determination of Organophosphate Esters in Aqueous Samples

    Directory of Open Access Journals (Sweden)

    Haiying Luo

    2014-01-01

    Full Text Available A new technique was established to identify eight organophosphate esters (OPEs in this work. It utilised dispersive liquid-liquid microextraction in combination with ultrahigh performance liquid chromatography/tandem mass spectrometry. The type and volume of extraction solvents, dispersion agent, and amount of NaCl were optimized. The target analytes were detected in the range of 1.0–200 µg/L with correlation coefficients ranging from 0.9982 to 0.9998, and the detection limits of the analytes were ranged from 0.02 to 0.07 µg/L (S/N=3. The feasibility of this method was demonstrated by identifying OPEs in aqueous samples that exhibited spiked recoveries, which ranged between 48.7% and 58.3% for triethyl phosphate (TEP as well as between 85.9% and 113% for the other OPEs. The precision was ranged from 3.2% to 9.3% (n=6, and the interprecision was ranged from 2.6% to 12.3% (n=5. Only 2 of the 12 selected samples were tested to be positive for OPEs, and the total concentrations of OPEs in them were 1.1 and 1.6 µg/L, respectively. This method was confirmed to be simple, fast, and accurate for identifying OPEs in aqueous samples.

  8. Behavior of supercooled aqueous solutions stemming from hidden liquid–liquid transition in water

    Energy Technology Data Exchange (ETDEWEB)

    Biddle, John W.; Holten, Vincent; Anisimov, Mikhail A., E-mail: anisimov@umd.edu [Institute for Physical Science and Technology and Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, Maryland 20742 (United States)

    2014-08-21

    A popular hypothesis that explains the anomalies of supercooled water is the existence of a metastable liquid–liquid transition hidden below the line of homogeneous nucleation. If this transition exists and if it is terminated by a critical point, the addition of a solute should generate a line of liquid–liquid critical points emanating from the critical point of pure metastable water. We have analyzed thermodynamic consequences of this scenario. In particular, we consider the behavior of two systems, H{sub 2}O-NaCl and H{sub 2}O-glycerol. We find the behavior of the heat capacity in supercooled aqueous solutions of NaCl, as reported by Archer and Carter [J. Phys. Chem. B 104, 8563 (2000)], to be consistent with the presence of the metastable liquid–liquid transition. We elucidate the non-conserved nature of the order parameter (extent of “reaction” between two alternative structures of water) and the consequences of its coupling with conserved properties (density and concentration). We also show how the shape of the critical line in a solution controls the difference in concentration of the coexisting liquid phases.

  9. Biodegradation of radioactive organic liquid waste from spent fuel reprocessing; Biodegradacao de rejeitos radioativos liquidos organicos provenientes do reprocessamento do combustivel nuclear

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Rafael Vicente de Padua

    2008-07-01

    The research and development program in reprocessing of low burn-up spent fuel elements began in Brazil in 70's, originating the lab-scale hot cell, known as Celeste located at Nuclear and Energy Research Institute, IPEN - CNEN/SP. The program was ended at the beginning of 90's, and the laboratory was closed down. Part of the radioactive waste generated mainly from the analytical laboratories is stored waiting for treatment at the Waste Management Laboratory, and it is constituted by mixture of aqueous and organic phases. The most widely used technique for the treatment of radioactive liquid wastes is the solidification in cement matrix, due to the low processing costs and compatibility with a wide variety of wastes. However, organics are generally incompatible with cement, interfering with the hydration and setting processes, and requiring pre -treatment with special additives to stabilize or destroy them. The objective of this work can be divided in three parts: organic compounds characterization in the radioactive liquid waste; the occurrence of bacterial consortia from Pocos de Caldas uranium mine soil and Sao Sebastiao estuary sediments that are able to degrade organic compounds; and the development of a methodology to biodegrade organic compounds from the radioactive liquid waste aiming the cementation. From the characterization analysis, TBP and ethyl acetate were chosen to be degraded. The results showed that selected bacterial consortia were efficient for the organic liquid wastes degradation. At the end of the experiments the biodegradation level were 66% for ethyl acetate and 70% for the TBP. (author)

  10. Headspace liquid-phase microextraction of methamphetamine and amphetamine in urine by an aqueous drop

    Energy Technology Data Exchange (ETDEWEB)

    He Yi [Department of Sciences, John Jay College of Criminal Justice, City University of New York, 445 W 59th Street, New York, NY 10019 (United States)]. E-mail: yhe@jjay.cuny.edu; Vargas, Angelica [Department of Sciences, John Jay College of Criminal Justice, City University of New York, 445 W 59th Street, New York, NY 10019 (United States); Kang, Youn-Jung [Department of Sciences, John Jay College of Criminal Justice, City University of New York, 445 W 59th Street, New York, NY 10019 (United States)

    2007-04-25

    This study developed a headspace liquid-phase microextraction (LPME) method by using a single aqueous drop in combination with high performance liquid chromatography (HPLC)-UV detection for the determination of methamphetamine (MAP) and amphetamine (AP) in urine samples. The analytes, volatile and basic, were released from sample matrix into the headspace first, and then protonated and dissolved in an aqueous H{sub 3}PO{sub 4} drop hanging in the headspace by a HPLC syringe. After extraction, this drop was directly injected into HPLC. Parameters affecting extraction efficiency were investigated and optimized. This method showed good linearity in the investigated concentration range of 1.0-1500 {mu}g L{sup -1}, repeatability of the extraction (R.S.D. < 5%, n = 6), and low detection limits (0.3 {mu}g L{sup -1} for both analytes). Enrichment factors of about 400-fold and 220-fold were achieved for MAP and AP, respectively, at optimum conditions. The feasibility of the method was demonstrated by analyzing human urine samples.

  11. DNA hybridization-induced reorientation of liquid crystal anchoring at the nematic liquid crystal/aqueous interface.

    Science.gov (United States)

    Price, Andrew D; Schwartz, Daniel K

    2008-07-01

    Interactions between DNA and an adsorbed cationic surfactant at the nematic liquid crystal (LC)/aqueous interface were investigated using polarized and fluorescence microscopy. The adsorption of octadecyltrimethylammonium bromide (OTAB) surfactant to the LC/aqueous interface resulted in homeotropic (untilted) LC alignment. Subsequent adsorption of single-stranded DNA (ssDNA) to the surfactant-laden interface modified the interfacial structure, resulting in a reorientation of the LC from homeotropic alignment to an intermediate tilt angle. Exposure of the ssDNA/OTAB interfacial complex to its ssDNA complement induced a second change in the interfacial structure characterized by the nucleation, growth, and coalescence of lateral regions that induced homeotropic LC alignment. Fluorescence microscopy showed explicitly that the complement was colocalized in the same regions as the homeotropic domains. Exposure to noncomplementary ssDNA caused no such response, suggesting that the homeotropic regions were due to DNA hybridization. This hybridization occurred in the vicinity of the interface despite the fact that the conditions in bulk solution were such that hybridization did not occur (high stringency), suggesting that the presence of the cationic surfactant neutralized electrostatic repulsion and allowed for hydrogen bonding between DNA complements. This system has potential for label-less and portable DNA detection. Indeed, LC response to ssDNA target was detected with a lower limit of approximately 50 fmol of complement and was sufficiently selective to differentiate a one-base-pair mismatch in a 16-mer target.

  12. Considerations affecting deep-well disposal of tritium-bearing low-level aqueous waste from nuclear fuel reprocessing plants

    Energy Technology Data Exchange (ETDEWEB)

    Trevorrow, L. E.; Warner, D. L.; Steindler, M. J.

    1977-03-01

    Present concepts of disposal of low-level aqueous wastes (LLAW) that contain much of the fission-product tritium from light water reactors involve dispersal to the atmosphere or to surface streams at fuel reprocessing plants. These concepts have been challenged in recent years. Deep-well injection of low-level aqueous wastes, an alternative to biospheric dispersal, is the subject of this presentation. Many factors must be considered in assessing its feasibility, including technology, costs, environmental impact, legal and regulatory constraints, and siting. Examination of these factors indicates that the technology of deep-well injection, extensively developed for other industrial wastes, would require little innovation before application to low-level aqueous wastes. Costs would be low, of the order of magnitude of 10/sup -4/ mill/kWh. The environmental impact of normal deep-well disposal would be small, compared with dispersal to the atmosphere or to surface streams; abnormal operation would not be expected to produce catastrophic results. Geologically suitable sites are abundant in the U.S., but a well would best be co-located with the fuel-reprocessing plant where the LLAW is produced. Legal and regulatory constraints now being developed will be the most important determinants of the feasibility of applying the method.

  13. Comparison of high-solids to liquid anaerobic co-digestion of food waste and green waste.

    Science.gov (United States)

    Chen, Xiang; Yan, Wei; Sheng, Kuichuan; Sanati, Mehri

    2014-02-01

    Co-digestion of food waste and green waste was conducted with six feedstock mixing ratios to evaluate biogas production. Increasing the food waste percentage in the feedstock resulted in an increased methane yield, while shorter retention time was achieved by increasing the green waste percentage. Food waste/green waste ratio of 40:60 was determined as preferred ratio for optimal biogas production. About 90% of methane yield was obtained after 24.5 days of digestion, with total methane yield of 272.1 mL/g VS. Based the preferred ratio, effect of total solids (TS) content on co-digestion of food waste and green waste was evaluated over a TS range of 5-25%. Results showed that methane yields from high-solids anaerobic digestion (15-20% TS) were higher than the output of liquid anaerobic digestion (5-10% TS), while methanogenesis was inhibited by further increasing the TS content to 25%. The inhibition may be caused by organic overloading and excess ammonia.

  14. Biological Information Document, Radioactive Liquid Waste Treatment Facility

    Energy Technology Data Exchange (ETDEWEB)

    Biggs, J.

    1995-12-31

    This document is intended to act as a baseline source material for risk assessments which can be used in Environmental Assessments and Environmental Impact Statements. The current Radioactive Liquid Waste Treatment Facility (RLWTF) does not meet current General Design Criteria for Non-reactor Nuclear Facilities and could be shut down affecting several DOE programs. This Biological Information Document summarizes various biological studies that have been conducted in the vicinity of new Proposed RLWTF site and an Alternative site. The Proposed site is located on Mesita del Buey, a mess top, and the Alternative site is located in Mortandad Canyon. The Proposed Site is devoid of overstory species due to previous disturbance and is dominated by a mixture of grasses, forbs, and scattered low-growing shrubs. Vegetation immediately adjacent to the site is a pinyon-juniper woodland. The Mortandad canyon bottom overstory is dominated by ponderosa pine, willow, and rush. The south-facing slope was dominated by ponderosa pine, mountain mahogany, oak, and muhly. The north-facing slope is dominated by Douglas fir, ponderosa pine, and oak. Studies on wildlife species are limited in the vicinity of the proposed project and further studies will be necessary to accurately identify wildlife populations and to what extent they utilize the project area. Some information is provided on invertebrates, amphibians and reptiles, and small mammals. Additional species information from other nearby locations is discussed in detail. Habitat requirements exist in the project area for one federally threatened wildlife species, the peregrine falcon, and one federal candidate species, the spotted bat. However, based on surveys outside of the project area but in similar habitats, these species are not expected to occur in either the Proposed or Alternative RLWTF sites. Habitat Evaluation Procedures were used to evaluate ecological functioning in the project area.

  15. The Effectivity of Marine Bio-activator and Surimi Liquid Waste Addition of Characteristics Liquid Organic Fertilizer from Sargassum sp.

    Directory of Open Access Journals (Sweden)

    Putri Wening Ratrinia

    2016-12-01

    Full Text Available Organic fertilizer is highly recommended for soil and plant because it can improve the productivity and repair physical, chemical, and biological of soil. Sargassum sp. and surimi liquid wastes contain organic matter and nutrient needed by plants and soils. The addition of marine bio-activator which contains bacterial isolates from litter mangrove serves to accelerate the composting time and increases the activity of microorganisms in the decomposition process. The purpose of this study was to determine optimum time and the best formulation of decomposition process organic fertilizer. Raw materials used a waste of seaweed Sargassum sp., marine bio-activator and surimi liquid waste from catfish (Clarias sp.. The research was conducted six treatments control, Sargassum sp. + marine bio-activator, surimi liquid waste , Sargassum sp. + marine bio-activator + surimi liquid waste 80%, 90%, 100%. All treatments were fermented for 9 days and analysed the C-organic, total N, C/N ratio, P2 O5 , K2 O on days 0, 3, 6 and 9. The results showed the optimum fermentation period was on the 6th day. The most optimum concentration of surimi liquid waste added was at a concentration of 90%, with characteristics of the products was C-organic 0.803 ± 0.0115 %, total N 740.063 ± 0.0862 ppm, C/N ratio 10.855 ± 0.1562, P2 O5 425.603 ± 0.2329 ppm, K2 O 2738.627 ± 0.2836 ppm.

  16. The Effectivity of Marine Bio-activator and Surimi Liquid Waste Addition of Characteristics Liquid Organic Fertilizer from Sargassum sp.

    Directory of Open Access Journals (Sweden)

    Putri Wening Ratrinia

    2017-02-01

    Full Text Available AbstractOrganic fertilizer is highly recommended for soil and plant because it can improve the productivity and repair physical, chemical, and biological of soil. Sargassum sp. and surimi liquid wastes contain organic matter and nutrient needed by plants and soils. The addition of marine bio-activator which contains bacterial isolates from litter mangrove serves to accelerate the composting time and increases the activity of microorganisms in the decomposition process. The purpose of this study was to determine optimum time and the best formulation of decomposition process organic fertilizer. Raw materials used a waste of seaweed Sargassum sp., marine bio-activator and surimi liquid waste from catfish (Clarias sp.. The research was conducted six treatments control, Sargassum sp. + marine bio-activator, surimi liquid waste , Sargassum sp. + marine bio-activator + surimi liquid waste 80%, 90%, 100%. All treatments were fermented for 9 days and analysed the C-organic, total N, C/N ratio, P2O5, K2O on days 0, 3, 6 and 9. The results showed the optimum fermentation period was on the 6th day. The most optimum concentration of surimi liquid waste added was at a concentration of 90%, with characteristics of the products was C-organic 0.803±0.0115%, total N 740.063±0.0862 ppm, C/N ratio 10.855±0.1562, P2O5 425.603±0.2329 ppm, K2O 2738.627±0.2836 ppm.

  17. Biosorption of Am-241 and Cs-137 by radioactive liquid waste by coffee husk

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Rafael Vicente de Padua; Sakata, Solange Kazumi; Bellini, Maria Helena; Marumo, Julio Takehiro, E-mail: jtmarumo@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-07-01

    Radioactive Waste Management Laboratory of Nuclear and Energy Research Institute, IPEN-CNEN/SP, has stored many types of radioactive liquid wastes, including liquid scintillators, mixed wastes from chemical analysis and spent decontamination solutions. These wastes need special attention, because the available treatment processes are often expensive and difficult to manage. Biosorption using biomass of vegetable using agricultural waste has become a very attractive technique because it involves the removal of heavy metals ions by low cost biossorbents. The aim of this study is to evaluate the potential of the coffee husk to remove Am-241 and Cs-137 from radioactive liquid waste. The coffee husk was tested in two forms, treated and untreated. The chemical treatment of the coffee husk was performed with HNO{sub 3} and NaOH diluted solutions. The results showed that the coffee husk did not showed significant differences in behavior and capacity for biosorption for Am-241 and Cs-137 over time. Coffee husk showed low biosorption capacity for Cs-137, removing only 7.2 {+-} 1.0% in 4 hours of contact time. For Am-241, the maximum biosorption was 57,5 {+-} 0.6% in 1 hours. These results suggest that coffee husk in untreated form can be used in the treatment of radioactive waste liquid containing Am-241. (author)

  18. Application of Waste Liquids Containing Lignin from Pulp-producing Industry to CWM Preparation

    Institute of Scientific and Technical Information of China (English)

    HUANG Ding-guo; TADAHIRO Murakata; TAKESHI Higuchi; SHIMIO Sato

    2004-01-01

    Three kinds of craft waste liquids, which are by-products in the pulp industry and contain much lignin,were used as dispersing additives for preparing Horonai coal CWM (coal water mixture). The experiments showed that the CWM exhibited the lowest viscosity when it was diluted with an appropriate amount of water with the waste eiquids added. The experiments also indicated that the maximum coal concentration in the 62.5% (mass fraction), and 56.5% is the maximum coal mass fraction of the CWM prepared without additives. These data show the effectiveness of the waste liquids as the additives for preparing CWMs. The zeta potential of coal particles in the CWMs changed with the addition of lignin. From the change, the steric repulsion effect of the lignin adsorbed on the coal particles is concluded to be mainly responsible for the CWM dispersion. The waste liquids contain less sulfur than PSSNa(polystyrene sulfonate sodium salt), a typical dispersant which is currently used for preparing the commercial CWM, when the sulfur content in the unit mass of the solid matters within the waste liquids is compared with that in unit mass of PSSNa. This fact suggests that the waste liquids are more advantageous than PSSNa as far as air pollutants are concerned.

  19. A Simple Approach to Characterize Gas-Aqueous Liquid Two-phase Flow Configuration Based on Discrete Solid-Liquid Contact Electrification.

    Science.gov (United States)

    Choi, Dongwhi; Lee, Donghyeon; Kim, Dong Sung

    2015-10-14

    In this study, we first suggest a simple approach to characterize configuration of gas-aqueous liquid two-phase flow based on discrete solid-liquid contact electrification, which is a newly defined concept as a sequential process of solid-liquid contact and successive detachment of the contact liquid from the solid surface. This approach exhibits several advantages such as simple operation, precise measurement, and cost-effectiveness. By using electric potential that is spontaneously generated by discrete solid-liquid contact electrification, the configurations of the gas-aqueous liquid two-phase flow such as size of a gas slug and flow rate are precisely characterized. According to the experimental and numerical analyses on parameters that affect electric potential, gas slugs have been verified to behave similarly to point electric charges when the measuring point of the electric potential is far enough from the gas slug. In addition, the configuration of the gas-aqueous liquid two-phase microfluidic system with multiple gas slugs is also characterized by using the presented approach. For a proof-of-concept demonstration of using the proposed approach in a self-triggered sensor, a gas slug detector with a counter system is developed to show its practicality and applicability.

  20. The Glycolysis of Poly(ethylene terephthalate) Waste: Lewis Acidic Ionic Liquids as High Efficient Catalysts

    OpenAIRE

    Mi Lin Zhang; Xue Feng Bai; Qun Feng Yue; Lin Fei Xiao

    2013-01-01

    Poly(ethlyene terephthalate) waste from a local market was depolymerized by ethylene glycol (EG) in the presence of Lewis acidic ionic liquids [Bmim]ZnCl3 and the qualitative analysis showed that bis(hydroxyethyl) terephthalate was the main product. Compared with ionic liquid [Bmim]Cl, the Lewis acidic ionic liquids showed highly catalytic activity in the glycolysis of poly(ethylene terephthalate) PET. Significantly, the conversion of PET and the yield of bis(hydroxyethyl) terephthalate were ...

  1. Stability of a nanofiltration membrane after contact with a low-level liquid radioactive waste

    Directory of Open Access Journals (Sweden)

    Elizabeth Eugenio de Mello Oliveira

    2013-01-01

    Full Text Available This study investigated the treatment of a liquid radioactive waste containing uranium (235U + 238U using nanofiltration membranes. The membranes were immersed in the waste for 24-5000 h, and their transport properties were evaluated before and after the immersion. Surface of the membranes changed after immersion in the waste. The SW5000 h specimen lost its coating layer of polyvinyl alcohol, and its rejection of sulfate ions and uranium decreased by about 35% and 30%, respectively. After immersion in the waste, the polyamide selective layer of the membranes became less thermally stable than that before immersion.

  2. Proceedings of waste stream minimization and utilization innovative concepts: An experimental technology exchange. Volume 2, Industrial liquid waste processing, industrial gaseous waste processing

    Energy Technology Data Exchange (ETDEWEB)

    Lee, V.E. [ed.; Watts, R.L.

    1993-04-01

    This two-volume proceedings summarize the results of fifteen innovations that were funded through the US Department of Energy`s Innovative Concept Program. The fifteen innovations were presented at the sixth Innovative Concepts Fair, held in Austin, Texas, on April 22--23, 1993. The concepts in this year`s fair address innovations that can substantially reduce or use waste streams. Each paper describes the need for the proposed concept, the concept being proposed, and the concept`s economics and market potential, key experimental results, and future development needs. The papers are divided into two volumes: Volume 1 addresses innovations for industrial solid waste processing and municipal waste reduction/recycling, and Volume 2 addresses industrial liquid waste processing and industrial gaseous waste processing. Individual reports are indexed separately.

  3. Theoretical and experimental investigation of aqueous liquids contained in carbon nanotubes

    Science.gov (United States)

    Yarin, Alexander L.; Yazicioglu, Almila G.; Megaridis, Constantine M.; Rossi, Maria Pia; Gogotsi, Yury

    2005-06-01

    The dynamic response—as caused by different means of thermal stimulation or pressurization—of aqueous liquid attoliter volumes contained inside carbon nanotubes is investigated theoretically and experimentally. The experiments indicate an energetically driven mechanism responsible for the dynamic multiphase fluid behavior visualized in real time with high spatial resolution using electron microscopy. The theoretical model is formulated using a continuum approach, which combines temperature-dependent mass diffusion with intermolecular interactions in the fluid bulk, as well as in the vicinity of the carbon walls. Intermolecular forces are modeled by Lennard-Jones potentials. Several one-dimensional and axisymmetric cases are considered. These include situations which physically represent liquid volume pinchoff, jetting, or fluid relocation due to thermal stimulation by a steady or modulated electron beam, as well as liquid precipitation (condensation) from vapor due to overcooling or pressurization. Comparisons between theoretical predictions and experimental data demonstrate the ability of the model to describe the characteristic trends observed in the experiments.

  4. New Standards in Liquid Waste Treatment at Fukushima Dai-ichi - 13134

    Energy Technology Data Exchange (ETDEWEB)

    Sylvester, Paul; Milner, Tim; Ruffing, Jennifer; Poole, Scott [EnergySolutions, 100 Center Point Circle, Suite 100, Center Point II, Columbia, SC 29210 (United States); Townson, Paul; Jensen, Jesse [EnergySolutions, 2345 Stevens Drive, Suite 240, Richland, WA 99354 (United States)

    2013-07-01

    The earthquake and tsunami on March 11, 2011 severely damaged the Fukushima Dai-ichi nuclear plant leading to the most severe nuclear incident since Chernobyl. Ongoing operations to cool the damaged reactors at the site have led to the generation of highly radioactive coolant water. This is currently mainly treated to remove Cs-137 and Cs-134 and passed through a reverse osmosis (RO) unit to reduce the salinity before being cycled back to the reactors. Because only the Cs isotopes are removed, the RO reject water still contains many radioactive isotopes and this has led to the accumulation of over 200,000 cubic meters (52 million gallons) of extremely contaminated water which is currently stored on site in tanks. EnergySolutions, in partnership with Toshiba, were contracted to develop a system to reduce 62 isotopes in this waste down to allowable levels. This was a significant technical challenge given the high background salt content of the wastewater, the variation in aqueous chemistry of the radioactive isotopes and the presence of non-active competing ions (e.g. Ca and Mg) which inhibit the removal of isotopes such as Sr-89 and Sr-90. Extensive testing was performed to design a suitable system that could meet the required decontamination goals. These tests were performed over a 6 month period at facilities available in the nearby Fukushima Dai-ni laboratory using actual waste samples. This data was then utilized to design a Multi Radioactive Nuclides Removal System (MRRS) for Fukushima which is a modified version of EnergySolutions' proprietary Advanced Liquid Processing System (ALPS)'. The stored tank waste is fed into a preliminary precipitation system where iron flocculation is performed to remove a number of isotopes, including Sb-125, Ru-106, Mn-54 and Co-60. The supernatant is then fed into a second precipitation tank where the pH is adjusted and the bulk of the Mg, Ca and Sr precipitated out as carbonates and hydroxides. After passing through a

  5. Biological conversion of the aqueous wastes from hydrothermal liquefaction of algae and pine wood by Rhodococci

    Energy Technology Data Exchange (ETDEWEB)

    He, Yucai; Li, Xiaolu; Xue, Xiaoyun; Swita, Marie S.; Schmidt, Andrew J.; Yang, Bin

    2017-01-01

    In this study, R. opacus PD630, R. jostii RHA1, R. jostii RHA1 VanA-, and their co-culture were employed to convert hydrothermal liquefaction aqueous waste (HTLAW) into lipids. After 11 days, the COD reduction of algal-HTLAW reached 93.4% and 92.7% by R. jostii RHA1 and its mutant VanA-, respectively. Woody-HTLAW promoted lipid accumulation of 0.43 g lipid/g cell dry weight in R. opacus PD630 cells. Additionally, the total number of chemicals in HTLAW decreased by over 1/3 after 7 days of coculture, and 0.10 g/L and 0.46 g/L lipids were incrementally accumulated in the cellular mass during the fermentation of wood- and algal-HTLAW, respectively. The GC-MS data supported that different metabolism pathways were followed when these Rhodococci strains degraded algae- and woody-HTLAW. These results indicated promising potential of bioconversion of under-utilized carbon and toxic compounds in HTLAW into useful products by selected Rhodococci.

  6. Commercial Coffee Wastes as Materials for Adsorption of Heavy Metals from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    George Z. Kyzas

    2012-10-01

    Full Text Available This work aims to study the removal of Cu(II and Cr(VI from aqueous solutions with commercial coffee wastes. Materials with no further treatment such as coffee residues from café may act as adsorbents for the removal of Cu(II and Cr(VI. Equilibrium data were successfully fitted to the Langmuir, Freundlich and Langmuir-Freundlich model (L-F. The maximum adsorption capacity of the coffee residues can reach 70 mg/g for the removal of Cu(II and 45 mg/g for Cr(VI. The kinetic data were fitted to pseudo-first, -second and -third order equations. The equilibrium was achieved in 120 min. Also, the effect of pH on adsorption and desorption was studied, as well as the influence of agitation rate. Ten cycles of adsorption-desorption were carried out revealing the strong reuse potential of these low-cost adsorbents; the latter was confirmed from a brief economic approach.

  7. Separation of aromatic precipitates from simulated high level radioactive waste by hydrolysis, evaporation and liquid-liquid extraction

    Energy Technology Data Exchange (ETDEWEB)

    Young, S.R.; Shah, H.B.; Carter, J.T.

    1991-01-01

    The Defense Waste Processing Facility (DWPF) at the SRS will be the United States' first facility to process High Level radioactive Waste (HLW) into a borosilicate glass matrix. The removal of aromatic precipitates by hydrolysis, evaporation and liquid-liquid extraction will be a key step in the processing of the HLW. This step, titled the Precipitate Hydrolysis Process, has been demonstrated by the Savannah River Laboratory with the Precipitate Hydrolysis Experimental Facility (PHEF). The mission of the PHEF is to demonstrate processing of simulated high level radioactive waste which contains tetraphenylborate precipitates and nitrite. Reduction of nitrite by hydroxylamine nitrate and hydrolysis of the tetraphenylborate by formic acid is discussed. Gaseous production, which is primarily benzene, nitrous oxide and carbon dioxide, has been quantified. Production of high-boiling organic compounds and the accumulation of these organic compounds within the process are addressed.

  8. Separation of aromatic precipitates from simulated high level radioactive waste by hydrolysis, evaporation and liquid-liquid extraction

    Energy Technology Data Exchange (ETDEWEB)

    Young, S.R.; Shah, H.B.; Carter, J.T.

    1991-12-31

    The Defense Waste Processing Facility (DWPF) at the SRS will be the United States` first facility to process High Level radioactive Waste (HLW) into a borosilicate glass matrix. The removal of aromatic precipitates by hydrolysis, evaporation and liquid-liquid extraction will be a key step in the processing of the HLW. This step, titled the Precipitate Hydrolysis Process, has been demonstrated by the Savannah River Laboratory with the Precipitate Hydrolysis Experimental Facility (PHEF). The mission of the PHEF is to demonstrate processing of simulated high level radioactive waste which contains tetraphenylborate precipitates and nitrite. Reduction of nitrite by hydroxylamine nitrate and hydrolysis of the tetraphenylborate by formic acid is discussed. Gaseous production, which is primarily benzene, nitrous oxide and carbon dioxide, has been quantified. Production of high-boiling organic compounds and the accumulation of these organic compounds within the process are addressed.

  9. Equilibrium, kinetic and thermodynamic studies for sorption of Ni (II) from aqueous solution using formaldehyde treated waste tea leaves

    OpenAIRE

    2015-01-01

    The sorption characteristic of Ni (II) from aqueous solution using formaldehyde treated waste tea leaves as a low cost sorbent has been studied. The effect of pH, contact time, sorbent dose, initial metal ion concentration and temperature were investigated in batch experiments. The equilibrium data were fitted into four most common isotherm models; Freundlich, Langmuir, Tempkin and Dubinin–Radushkevich (D–R). The Langmuir model described the sorption isotherm best with maximum monolayer sorpt...

  10. Influence of liquid structure on diffusive isotope separation in molten silicates and aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Watkins, J.M.; DePaolo, D.J.; Ryerson, F.J.; Peterson, B.

    2011-03-01

    }/D{sub Si}. Cations diffusing in aqueous solutions display a similar relationship between isotopic separation efficiency and D{sub cation} =D{sub H 2 O} , although the efficiencies are smaller than in silicate liquids. Our empirical relationship provides a tool for predicting the magnitude of diffusive isotopic effects in many geologic environments and a basis for a more comprehensive theory of isotope separation in liquid solutions. We present a conceptual model for the relationship between diffusivity and liquid structure that is consistent with available data.

  11. Liquid and Gaseous Waste Operations Project Annual Operating Report CY 1999

    Energy Technology Data Exchange (ETDEWEB)

    Maddox, J.J.; Scott, C.B.

    2000-03-01

    A total of 5.77 x 10 7 gallons (gal) of liquid waste was decontaminated by the Process Waste Treatment Complex (PWTC) - Building 3544 ion exchange system during calendar year (CY) 1999. This averaged to 110 gpm throughout the year. An additional 3.94 x 10 6 gal of liquid waste (average of 8 gpm throughout the year) was decontaminated using the zeolite treatment system due to periods of high Cesium levels in the influent wastewater. A total of 6.17 x 10 7 gal of liquid waste (average of 118 gpm throughout the year) was decontaminated at Building 3544 during the year. During the year, the regeneration of the ion exchange resins resulted in the generation of 8.00 x 10 3 gal of Liquid Low-Level Waste (LLLW) concentrate and 9.00 x 10 2 gal of LLLW supernate. See Table 1 for a monthly summary of activities at Building 3544. Figure 1 shows a diagram of the Process Waste Collection and Transfer System and Figure 2 shows a diagram of the Building 3544 treatment process. Figures 3, 4 5, and 6 s how a comparison of operations at Building 3544 in 1997 with previous years. Figure 7 shows a comparison of annual rainfall at Oak Ridge National Laboratory (ORNL) since 1995.

  12. Removal of Heavy Metals from Liquid Laboratory Waste Using Precipitation and Adsorption Methods

    Directory of Open Access Journals (Sweden)

    Nastiti Siswi Indrasti

    2010-04-01

    Full Text Available Liquid laboratory waste (such as residue of Chemical Oxygen Demand/COD analysis contains high concentration of heavy metals (mercury/Hg, silver/Ag and chrome/Cr and has a high potential to pollute the environment. The liquid waste generated by laboratories is generally in small quantity, but it is extremely toxic. It is urgently in need to find out an appropriate method to reduce the problems according to the liquid waste characteristics. In this research work, precipitation and adsorption methods were evaluated to remove Hg, Ag and Cr from liquid laboratory waste, covering determination of optimum process conditions, levels of removal and achievable treated waste quality. Results showed that a Cr removal of 97% was obtained by pH 10, and Hg and Ag removals of 97-99% were reached by pH 12. Although heavy metals removals using precipitation was very significant, but the concentration of heavy metals in the treated waste was still high (0.73-2.62 mg/L and need for further treatment. Applying activated carbon adsorption for further treatment of the effluent reduced dissolved heavy metals to 0-0.05 mg/L, depending on the type of heavy metals as well as the type and dosing of activated carbon.

  13. Solidification of radioactive liquid wastes. A comparison of treatment options for spent resins and concentrates

    Energy Technology Data Exchange (ETDEWEB)

    Roth, A. [Hansa Projekt Anlagentechnik GmbH, Hamburg (Germany); Willmann, F. [Westinghouse Electric Germany GmbH, Mannheim (Germany); Ebata, M. [Toshiba Corporation Power Systems Company, Isogo-Ku, Yokohama (Japan); Wendt, S. [Hansa Projekt Anlagentechnik GmbH, Hamburg (Germany)

    2008-07-01

    Ion exchange is one of the most common and effective treatment methods for liquid radioactive waste. However, spent ion exchange resins are considered to be problematic waste that in many cases require special approaches and pre-conditioning during its immobilization to meet the acceptance criteria for disposal. Because of the function that they fulfill, spent ion exchange resins often contain high concentrations of radioactivity and pose special handling and treatment problems. Another very common method of liquid radioactive waste treatment and water cleaning is the evaporation or diaphragm filtration. Both treatment options offer a high volume reduction of the total volume of liquids treated but generate concentrates which contain high concentrations of radioactivity. Both mentioned waste streams, spent resins as well as concentrates, resulting from first step liquid radioactive waste treatment systems have to be conditioned in a suitable manner to achieve stable waste products for final disposal. The most common method of treatment of such waste streams is the solidification in a solid matrix with additional inactive material like cement, polymer etc. In the past good results have been achieved and the high concentration of radioactivity can be reduced by adding the inactive material. On the other hand, under the environment of limited space for interim storage and the absence of a final repository site, the built-up of additional volume has to be considered as very critical. Moreover, corrosive effects on cemented drums during long-term interim storage at the surface have raised doubts about the long-term stability of such waste products. In order to avoid such disadvantages solidification methods have been improved in order to get a well-defined product with a better load factor of wastes in the matrix. In a complete different approach, other technologies solidify the liquid radioactive wastes without adding of any inactive material by means of drying

  14. Absorption of carbon dioxide in aqueous solutions of imidazolium ionic liquids with carboxylate anions

    Energy Technology Data Exchange (ETDEWEB)

    Baj, Stefan; Krawczyk, Tomasz; Dabrowska, Aleksandra; Siewniak, Agnieszka [Silesian University of Technology, Gliwice (Poland); Sobolewski, Aleksander [Institute for Chemical Processing of Coal, Zabrze (Poland)

    2015-11-15

    The solubility of carbon dioxide at atmospheric pressure in aqueous mixtures of 1,3-alkyl substituted imidazolium ionic liquids (ILs) containing carboxylic anions was studied. The ILs showed increased solubility of CO{sub 2} with decreasing water concentration. The relationship between the CO{sub 2} concentration in solution and the mole fraction of water in the ILs describes a sigmoidal curve. The regression constants of a logistic function were used to quantitatively assess the absorbent capacity and the effect of water on CO{sub 2} absorption. ILs containing the most basic anions, such as pivalate, propionate and acetate, had the best properties. It was observed that the impact of water on absorption primarily depended on the cation structure. The best absorption performance was observed for 1,3-dibutylimidazolium pivalate and 1-butyl-3-methyl imidazolium acetate.

  15. Development of a test system for high level liquid waste partitioning

    Directory of Open Access Journals (Sweden)

    Duan Wu H.

    2015-01-01

    Full Text Available The partitioning and transmutation strategy has increasingly attracted interest for the safe treatment and disposal of high level liquid waste, in which the partitioning of high level liquid waste is one of the critical technical issues. An improved total partitioning process, including a tri-alkylphosphine oxide process for the removal of actinides, a crown ether strontium extraction process for the removal of strontium, and a calixcrown ether cesium extraction process for the removal of cesium, has been developed to treat Chinese high level liquid waste. A test system containing 72-stage 10-mm-diam annular centrifugal contactors, a remote sampling system, a rotor speed acquisition-monitoring system, a feeding system, and a video camera-surveillance system was successfully developed to carry out the hot test for verifying the improved total partitioning process. The test system has been successfully used in a 160 hour hot test using genuine high level liquid waste. During the hot test, the test system was stable, which demonstrated it was reliable for the hot test of the high level liquid waste partitioning.

  16. Recovery of hydrocarbon liquid from waste high density polyethylene by thermal pyrolysis

    Directory of Open Access Journals (Sweden)

    Sachin Kumar

    2011-12-01

    Full Text Available Thermal degradation of waste plastics in an inert atmosphere has been regarded as a productive method, because this process can convert waste plastics into hydrocarbons that can be used either as fuels or as a source of chemicals. In this work, waste high-density polyethylene (HDPE plastic was chosen as the material for pyrolysis. A simple pyrolysis reactor system has been used to pyrolyse waste HDPE with the objective of optimizing the liquid product yield at a temperature range of 400ºC to 550ºC. Results of pyrolysis experiments showed that, at a temperature of 450ºC and below, the major product of the pyrolysis was oily liquid which became a viscous liquid or waxy solid at temperatures above 475ºC. The yield of the liquid fraction obtained increased with the residence time for waste HDPE. The liquid fractions obtained were analyzed for composition using FTIR and GC-MS. The physical properties of the pyrolytic oil show the presence of a mixture of different fuel fractions such as gasoline, kerosene and diesel in the oil.

  17. Selectivity of NF membrane for treatment of liquid waste containing uranium

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Elizabeth E.M.; Barbosa, Celina C.R., E-mail: eemo@ien.gov.br [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil); Afonso, Julio C., E-mail: julio@iq.ufrj.br [Universidade Federal do Rio de Janeiro(UFRJ), Rio de Janeiro, RJ (Brazil). Inst. de Quimica. Dept. de Quimica

    2013-07-01

    The performance of two nanofiltration membranes were investigated for treatment of liquid waste containing uranium through two conditions permeation: permeation test and concentration test of the waste. In the permeation test solution permeated returned to the feed tank after collected samples each 3 hours. In the test of concentration the permeated was collected continuously until 90% reduction of the feed volume. The liquid waste ('carbonated water') was obtained during conversion of UF{sub 6} to UO{sub 2} in the cycle of nuclear fuel. This waste contains uranium concentration on average 7.0 mg L{sup -1}, and not be eliminated to the environmental. The waste was permeated using a cross-flow membrane cell in the pressure of the 1.5 MPa. The selectivity of the membranes for separation of uranium was between 83% and 90% for both tests. In the concentration tests the waste was concentrated around for 5 times. The surface layer of the membranes was evaluated before and after the tests by infrared spectroscopy (ATR-FTIR), field emission microscopy (FESEM) and atomic force spectroscopy (AFM). The membrane separation process is a technique feasible to and very satisfactory for treatment the liquid waste. (author)

  18. Electrical conductivity study on micelle formation of long-chain imidazolium ionic liquids in aqueous solution.

    Science.gov (United States)

    Inoue, Tohru; Ebina, Hayato; Dong, Bin; Zheng, Liqiang

    2007-10-01

    Electrical conductivity was measured for aqueous solutions of long-chain imidazolium ionic liquids (IL), 1-alkyl-3-methylimidazolium bromides with C(12)-C(16) alkyl chains. The break points appeared in specific conductivity (kappa) vs concentration (c) plot indicates that the molecular aggregates, i.e., micelles, are formed in aqueous solutions of these IL species. The critical micelle concentration (cmc) determined from the kappa vs c plot is somewhat lower than those for typical cationic surfactants, alkyltrimethylammonium bromides with the same hydrocarbon chain length. The electrical conductivity data were analyzed according to the mixed electrolyte model of micellar solution, and the aggregation number, n, and the degree of counter ion binding, beta, were estimated. The n values of the present ILs are somewhat smaller than those reported for alkyltrimethylammonium bromides, which may be attributed to bulkiness of the cationic head group of the IL species. The thermodynamic parameters for micelle formation of the present ILs were estimated using the values of cmc and beta as a function of temperature. The contribution of entropy term to the micelle formation is superior to that of enthalpy term below about 30 degrees C, and it becomes opposite at higher temperature. This coincides with the picture drawn for the micelle formation of conventional ionic surfactants.

  19. Bile acid-surfactant interactions at the liquid crystal/aqueous interface.

    Science.gov (United States)

    He, Sihui; Liang, Wenlang; Cheng, Kung-Lung; Fang, Jiyu; Wu, Shin-Tson

    2014-07-14

    The interaction between bile acids and surfactants at interfaces plays an important role in fat digestion. In this paper, we study the competitive adsorption of cholic acid (CA) at the sodium dodecyl sulfate (SDS)-laden liquid crystal (LC)/aqueous interface formed with cyanobiphenyl (nCB, n = 5-8) and the mixture of 5CB with 4-(4-pentylcyclohexyl)benzonitrile (5PCH). We find that the critical concentration of CA required to displace SDS from the interface linearly decreases from 160 μM to 16 μM by reducing the alkyl chain length of nCB from n = 8 to n = 5 and from 16 μM to 1.5 μM by increasing the 5PCH concentration from 0 wt% to 19 wt% in the 5PCH-5CB binary mixture. Our results clearly demonstrate that the sensitivity of 5PCH-5CB mixtures for monitoring the interaction between CA and SDS at the LC/aqueous interface can be increased by one order of magnitude, compared to 5CB.

  20. Development of counter current salting-out homogenous liquid-liquid extraction for isolation and preconcentration of some pesticides from aqueous samples.

    Science.gov (United States)

    Farajzadeh, Mir Ali; Feriduni, Behruz; Afshar Mogaddam, Mohammad Reza

    2015-07-23

    In this paper, a new version of salting-out homogenous liquid-liquid extraction based on counter current mode combined with dispersive liquid-liquid microextraction has been developed for the extraction and preconcentration of some pesticides from aqueous samples and their determination by gas chromatography-flame ionization detection. In order to perform the method, aqueous solution of the analytes containing acetonitrile and 1,2-dibromoethane is transferred into a narrow bore tube which is filled partially with NaCl. During passing the solution through the tube, fine droplets of the organic phase are produced at the interface of solution and salt which go up through the tube and form a separated layer on the aqueous phase. The collected organic phase is removed and injected into de-ionized water for more enrichment of the analytes. Under the optimum extraction conditions, the method shows broad linear ranges for the target analytes. Enrichment factors and limits of detection for the selected pesticides are obtained in the ranges of 3480-3800 and 0.1-5μgL(-1), respectively. Relative standard deviations are in the range of 2-7% (n=6, C=50 or 100μgL(-1), each analyte). Finally, some aqueous samples were successfully analyzed using the developed method.

  1. Optimization of Copper Removal from Aqueous Solutions Using Emulsion Liquid Membranes with Benzoylacetone as a Carrier

    Directory of Open Access Journals (Sweden)

    Loreto León

    2017-01-01

    Full Text Available The presence of heavy metals in aqueous solutions above certain limits represents a serious threat to the environment due to their toxicity and non-degradability. Thus, the removal of these metals from contaminated waters has received increasing attention during recent decades. This paper describes the removal of Cu(II from aqueous solutions by emulsion liquid membranes, through a carrier-facilitated counter-transport mechanism, using benzoylacetone as the carrier and HCl as the stripping agent (protons as counter-ions. To optimize the Cu(II removal process, the effect of the following operating parameters on the on the stability of the emulsion liquid membrane and on the Cu(II removal efficiency was studied: feed pH, HCl concentration in the permeate phase, carrier and emulsifier concentration in the membrane phase, feed phase/emulsion phase and permeate phase/membrane phase volume ratios, emulsification time and speed in the primary emulsion preparation and stirring speed in the whole feed phase/emulsion phase system. Typical membrane transport parameters, such as flux and permeability, were also determined. Optimal Cu(II removal conditions were: 5.5 feed pH, 10 kg/m3 benzoylacetone concentration in the membrane phase, 18.250 kg/m3 HCl concentration in the permeate phase, 50 kg/m3 Span 80 concentration in the membrane phase, 200 rpm stirring rate, 5 min emulsification time, 2700 rpm emulsification rate, 2:1 feed:emulsion volume ratio and 1:1 permeate:membrane volume ratio. In these optimal conditions, 80.3% of Cu(II was removed in 15 min with an apparent initial flux and permeability of 0.3384 kg·m−3·min−1 and 0.3208 min−1, respectively.

  2. Simultaneous determination of dorzolomide and timolol in aqueous humor: a novel salting out liquid-liquid microextraction combined with HPLC.

    Science.gov (United States)

    Mohamed, Abdel-Maaboud Ismail; Abdel-Wadood, Hanaa Mohammed; Mousa, Heba Salah

    2014-12-01

    A Snovel method for the simultaneous separation and determination of two antiglaucoma drugs namely, dorzolamide hydrochloride (DOR) and timolol maleate (TIM) in aqueous humor samples (AH) was developed by using salting-out assisted liquid-liquid microextraction (SALLME) combined with HPLC-UV method. Box-Behnken experimental design and response surface methodology were employed to assist the optimization of SALLME conditions, including salt concentration, the pH of sample solution and vortex time as variable factors. The optimal extraction conditions were as follows: to 50 µL of AH sample, 100 µL of phosphate buffer (100 mmol L(-1), pH 11.9), 90 µL of acetonitrile (ACN) and 0.11 g of (NH4)2SO4 salt were added into an Eppendorf vial (1 mL) then vortexed for 1.1 min. As an effort to miniaturize SALLE system, a 1 mL syringe adapted with a capillary tube was employed as the phase separation device. Once the phase separation occurred, the upper layer could be narrowed into the capillary tube by pushing the plunger; thus, the collection of the upper layer solvent was simple and convenient. By miniaturization, the consumption of the organic solvent was decreased as low as possible. The chromatographic separation was achieved on Gemini C18 column using a mobile phase of ACN: 30 mmol L(-1) potassium dihydrogen phosphate buffer containing 0.1% triethylamine, pH 3.5 (20:80, v/v) at a flow rate of 1 mL min(-1) and UV detection at 254 and 295 nm for DOR and TIM, respectively. Mepivacaine hydrochloride was used as an internal standard. The described method showed better separation with enhanced sensitivities than the previously reported methods with limits of quantitation of 8.75 and 10.32 ng mL(-1) in aqueous solution and 15.97 and 23.53 ng mL(-1) in AH for DOR and TIM, respectively. The simple, rapid and eco-friendly SALLME-HPLC method has been successfully applied for the simultaneous pharmacokinetic studies of DOR and TIM in rabbit AH.

  3. Combustion of animal or vegetable based liquid waste products; Foerbraenning av flytande animaliska/vegetabiliska restprodukter

    Energy Technology Data Exchange (ETDEWEB)

    Wikman, Karin; Berg, Magnus [AaF-Energikonsult AB, Stockholm (Sweden)

    2002-04-01

    In this project experiences from combustion of animal and vegetable based liquid waste products have been compiled. Legal aspects have also been taken into consideration and the potential for this type of fuel on the Swedish energy market has been evaluated. Today the supply of animal and vegetable based liquid waste products for energy production in Sweden is limited. The total production of animal based liquid fat is about 10,000 tonnes annually. The animal based liquid waste products origin mainly from the manufacturing of meat and bone meal. Since meat and bone meal has been banned from use in animal feeds it is possible that the amount of animal based liquid fat will decrease. The vegetable based liquid waste products that are produced in the processing of vegetable fats are today used mainly for internal energy production. This result in limited availability on the commercial market. The potential for import of animal and vegetable based liquid waste products is estimated to be relatively large since the production of this type of waste products is larger in many other countries compared to Sweden. Vegetable oils that are used as food or raw material in industries could also be imported for combustion, but this is not reasonable today since the energy prices are relatively low. Restrictions allow import of SRM exclusively from Denmark. This is today the only limit for increased imports of animal based liquid fat. The restrictions for handle and combustion of animal and vegetable based liquid waste products are partly unclear since this is covered in several regulations that are not easy to interpret. The new directive for combustion of waste (2000/76/EG) is valid for animal based waste products but not for cadaver or vegetable based waste products from provisions industries. This study has shown that more than 27,400 tonnes of animal based liquid waste products and about 6,000 tonnes of vegetable based liquid waste products were used for combustion in Sweden

  4. Emulsion of aqueous-based nonspherical droplets in aqueous solutions by single-chain surfactants: templated assembly by nonamphiphilic lyotropic liquid crystals in water.

    Science.gov (United States)

    Varghese, Nisha; Shetye, Gauri S; Bandyopadhyay, Debjyoti; Gobalasingham, Nemal; Seo, JinAm; Wang, Jo-Han; Theiler, Barbara; Luk, Yan-Yeung

    2012-07-24

    Single-chain surfactants usually emulsify and stabilize oily substances into droplets in an aqueous solution. Here, we report a coassembly system, in which single types of anionic or non-ionic surfactants emulsify a class of water-soluble nonamphiphilic organic salts with fused aromatic rings in aqueous solutions. The nonamphiphilic organic salts are in turn promoted to form droplets of water-based liquid crystals (chromonic liquid crystals) encapsulated by single-chain surfactants. The droplets, stabilized against coalescence by encapsulated in a layer (or layers) of single chain surfactants, are of both nonspherical tactoid (elongated ellipsoid with pointy ends) and spherical shapes. The tactoids have an average long axis of ∼9 μm and a short axis of ∼3.5 μm with the liquid crystal aligning parallel to the droplet surface. The spherical droplets are 5-10 μm in diameter and have the liquid crystal aligning perpendicular to the droplet surface and a point defect in the center. Cationic and zwitterionic surfactants studied in this work did not promote the organic salt to form droplets. These results illustrate the complex interplay of self-association and thermodynamic incompatibility of molecules in water, which can cause new assembly behavior, including potential formation of vesicles or other assemblies, from surfactants that usually form only micelles. These unprecedented tactoidal shaped droplets also provide potential for the fabrication of new soft organic microcapsules.

  5. Protein remains stable at unusually high temperatures when solvated in aqueous mixtures of amino acid based ionic liquids

    DEFF Research Database (Denmark)

    Chevrot, Guillaume; Fileti, Eudes Eterno; Chaban, Vitaly V.

    2016-01-01

    [EMIM][TRP] (5 mol% in water). Upon analyzing the radius of gyration, the solvent-accessible surface area, root-mean-squared deviations, and inter- and intramolecular hydrogen bonds, we found that the mini-protein remains stable at 30–40 K higher temperatures in aqueous amino acid based ionic liquids...

  6. Momentum, Heat, and Neutral Mass Transport in Convective Atmospheric Pressure Plasma-Liquid Systems and Implications for Aqueous Targets

    CERN Document Server

    Lindsay, Alexander; Slikboer, Elmar; Shannon, Steven; Graves, David

    2015-01-01

    There is a growing interest in the study of plasma-liquid interactions with application to biomedicine, chemical disinfection, agriculture, and other fields. This work models the momentum, heat, and neutral species mass transfer between gas and aqueous phases in the context of a streamer discharge; the qualitative conclusions are generally applicable to plasma-liquid systems. The problem domain is discretized using the finite element method. The most interesting and relevant model result for application purposes is the steep gradients in reactive species at the interface. At the center of where the reactive gas stream impinges on the water surface, the aqueous concentrations of OH and ONOOH decrease by roughly 9 and 4 orders of magnitude respectively within 50 $\\mu$m of the interface. Recognizing the limited penetration of reactive plasma species into the aqueous phase is critical to discussions about the therapeutic mechanisms for direct plasma treatment of biological solutions. Other interesting results fro...

  7. CO2 sequestration using waste concrete and anorthosite tailings by direct mineral carbonation in gas-solid-liquid and gas-solid routes.

    Science.gov (United States)

    Ben Ghacham, Alia; Cecchi, Emmanuelle; Pasquier, Louis-César; Blais, Jean-François; Mercier, Guy

    2015-11-01

    Mineral carbonation (MC) represents a promising alternative for sequestering CO2. In this work, the CO2 sequestration capacity of the available calcium-bearing materials waste concrete and anorthosite tailings is assessed in gas-solid-liquid and gas-solid routes using 18.2% flue CO2 gas. The objective is to screen for a better potential residue and phase route and as the ultimate purpose to develop a cost-effective process. The results indicate the possibility of removing 66% from inlet CO2 using waste concrete for the aqueous route. However, the results that were obtained with the carbonation of anorthosite were less significant, with 34% as the maximal percentage of CO2 removal. The difference in terms of reactivity could be explained by the accessibility to calcium. In fact, anorthosite presents a framework structure wherein the calcium is trapped, which could slow the calcium dissolution into the aqueous phase compared to the concrete sample, where calcium can more easily leach. In the other part of the study concerning gas-solid carbonation, the results of CO2 removal did not exceed 15%, which is not economically interesting for scaling up the process. The results obtained with waste concrete samples in aqueous phase are interesting. In fact, 34.6% of the introduced CO2 is converted into carbonate after 15 min of contact with the gas without chemical additives and at a relatively low gas pressure. Research on the optimization of the aqueous process using waste concrete should be performed to enhance the reaction rate and to develop a cost-effective process.

  8. Subsides for optimization of transfer of radioactive liquid waste from {sup 99}MO production plant to the waste treatment facility

    Energy Technology Data Exchange (ETDEWEB)

    Rego, Maria Eugenia de Melo; Vicente, Roberto; Hiromoto, Goro, E-mail: maria.eugenia@ipen.br, E-mail: rvicente@ipen.br, E-mail: hiromoto@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    The increasing need for radioisotopes lead Brazil to consider the domestic production of {sup 99}Mo from fission of low enriched uranium targets. In order to meet the present demand of {sup 99m}Tc generators the planned 'end of irradiation' activity of {sup 99}Mo is about 170 TBq per week. The radioactive waste from the production plant will be transferred to a waste treatment facility at the same site. The total activity of the actinides, fission and activation products present in the waste were predicted based on the fission yield and activation data for the irradiation conditions, such as composition and mass of uranium targets, irradiation time, neutron flux, production process and schedule, already established by the project management. The transfer of the waste from the production plant to the treatment facility will be done by means of special shielded packages. In the present study, the commercially available code Scale 6.0 was used to simulate the irradiation of the targets and the decay of radioactive products, assuming that an alkaline dissolution process would be performed on the targets before the removal and purification of {sup 99}Mo. The assessment of the shielding required for the packages containing liquid waste was done using MicroShield 9 code. The results presented here are part of a project that aims at contributing to the design of the waste management system for the {sup 99}Mo production facility. (author)

  9. Statistical Description of Liquid Low-Level Waste System Transssuranic Wastes at Oak Ridge Nation Laboratory, Oak Ridge, Tennessee

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-12-01

    The US DOE has presented plans for processing liquid low-level wastes (LLLW) located at Oak Ridge National Laboratory (ORNL) in the LLLW tank system. These wastes are among the most hazardous on the Oak Ridge reservation and exhibit both RCRA toxic and radiological hazards. The Tennessee Department of Health and Environment has mandated that the processing of these wastes must begin by the year 2002 and the the goal should be permanent disposal at a site off the Oak Ridge Reservation. To meet this schedule, DOE will solicit bids from various private sector companies for the construction of a processing facility on land located near the ORNL Melton Valley Storage Tanks to be operated by the private sector on a contract basis. This report will support the Request for Proposal process and will give potential vendors information about the wastes contained in the ORNL tank farm system. The report consolidates current data about the properties and composition of these wastes and presents methods to calculate the error bounds of the data in the best technically defensible manner possible. The report includes information for only the tank waste that is to be included in the request for proposal.

  10. FY 1995 separation studies for liquid low-level waste treatment at Oak Ridge National Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Bostick, D.T.; Arnold, W.D.; Burgess, M.W. [and others

    1995-01-01

    During FY 1995, studies were continued to develop improved methods for centralized treatment of liquid low-level waste (LLLW) at Oak Ridge National Laboratory (ORNL). Focus in this reporting period was on (1) identifying the parameters that affect the selective removal of {sup 90}Sr and {sup 137}Cs, two of the principal radioactive contaminants expected in the waste; (2) validating the effectiveness of the treatment methods by testing an ac Melton Valley Storage Tank (MVST) supernate; (3) evaluating the optimum solid/liquid separation techniques for the waste; (4) identifying potential treatment methods for removal of technetium from LLLW; and (5) identifying potential methods for stabilizing the high-activity secondary solid wastes generated by the treatment.

  11. Validation of method for determination of different classes of pesticides in aqueous samples by dispersive liquid-liquid microextraction with liquid chromatography-tandem mass spectrometric detection.

    Science.gov (United States)

    Caldas, Sergiane Souza; Costa, Fabiane Pinho; Primel, Ednei Gilberto

    2010-04-14

    In this study, a simple, rapid and efficient method has been developed for the extraction and preconcentration of different classes of pesticides, carbofuran (insecticide), clomazone (herbicide) and tebuconazole (fungicide) in aqueous samples by dispersive liquid-liquid microextraction (DLLME) coupled with liquid chromatography-tandem mass spectrometric detection. Some experimental parameters that influence the extraction efficiency, such as the type and volume of the disperser solvents and extraction solvents, extraction time, speed of centrifugation, pH and addition of salt were examined and optimized. Under the optimum conditions, the recoveries of pesticides in water at spiking levels between 0.02 and 2.0 microg L(-1) ranged from 62.7% to 120.0%. The relative standard deviations varied between 1.9% and 9.1% (n=3). The limits of quantification of the method considering a 50-fold preconcentration step were 0.02 microg L(-1). The linearity of the method ranged from 1.0 to 1000 microg L(-1) for all compounds, with correlation coefficients varying from 0.9982 to 0.9992. Results show that the method we propose can meet the requirements for the determination of pesticides in water samples. The comparison of this method with solid-phase extraction indicates that DLLME is a simple, fast, and low-cost method for the determination of pesticides in natural waters.

  12. Determination of Sudan I-IV in candy using ionic liquid/anionic surfactant aqueous two-phase extraction coupled with high-performance liquid chromatography.

    Science.gov (United States)

    Yu, Wei; Liu, Zhongling; Li, Qiang; Zhang, Hanqi; Yu, Yong

    2015-04-15

    Ionic liquid/anionic surfactant aqueous two-phase system was developed and applied for the extraction of Sudan I-IV. High-performance liquid chromatography was applied to the determination of the analytes. The aqueous two-phase system (ATPS) was formed in the present of C4[MIM]BF4, sodium dodecyl benzene sulphonate and (NH4)2SO4. The parameters affecting the extraction efficiency, such as volume of ionic liquid, amount of sodium dodecyl benzene sulphonate, ionic strength, pH value of system, extraction time and temperature were investigated. The limits of detection for Sudan I, II, III and IV were 5.45, 4.66, 3.68, 4.20 μg kg(-1), respectively. When the present method was applied to the analysis of candy samples, the recoveries of the analytes ranged from 82.3% to 112.1% and relative standard deviations were lower than 7.41%.

  13. Containment and recovery of a light non-aqueous phase liquid plume at a woodtreating facility

    Energy Technology Data Exchange (ETDEWEB)

    Crouse, D. [Roy F. Weston, Inc., Edison, NJ (United States); Powell, G. [Environmental Protection Agency, Cincinnati, OH (United States); Hawthorn, S. [Environmental Protection Agency, Cincinnati, OH (United States); Weinstock, S. [Environmental Protection Agency, Butte, MT (United States)

    1997-12-31

    A woodtreating site in Montana used a formulation (product) of 5 percent pentachlorophenol and 95 percent diesel fuel as a carrier liquid to pressure treat lumber. Through years of operations approximately 378,500 liters of this light non-aqueous phase liquid (LNAPL) product spilled onto the ground and soaked into the groundwater. A plume of this LNAPL product flowed in a northerly direction toward a stream located approximately 410 meters from the pressure treatment building. A 271-meter long high density polyethylene (HDPE) containment cutoff barrier wall was installed 15 meters from the stream to capture, contain, and prevent the product from migrating off site. This barrier was extended to a depth of 3.7 meters below ground surface and allowed the groundwater to flow beneath it. Ten product recovery wells, each with a dual-phase pumping system, were installed within the plume, and a groundwater model was completed to indicate how the plume would be contained by generating a cone of influence at each recovery well. The model indicated that the recovery wells and cutoff barrier wall would contain the plume and prevent further migration. To date, nearly 3{1/2} year`s later, approximately 106,000 liters of product have been recovered.

  14. Interactions of Aqueous Imidazolium-Based Ionic Liquid Mixtures with Solid-Supported Phospholipid Vesicles

    Science.gov (United States)

    Losada-Pérez, Patricia; Khorshid, Mehran; Renner, Frank Uwe

    2016-01-01

    Despite the environmentally friendly reputation of ionic liquids (ILs), their safety has been recently questioned given their potential as cytotoxic agents. The fundamental mechanisms underlying the interactions between ILs and cells are less studied and by far not completely understood. Biomimetic films are here important biophysical model systems to elucidate fundamental aspects and mechanisms relevant for a large range of biological interaction ranging from signaling to drug reception or toxicity. Here we use dissipative quartz crystal microbalance QCM-D to examine the effect of aqueous imidazolium-based ionic liquid mixtures on solid-supported biomimetic membranes. Specifically, we assess in real time the effect of the cation chain length and the anion nature on a supported vesicle layer of the model phospholipid DMPC. Results indicate that interactions are mainly driven by the hydrophobic components of the IL, which significantly distort the layer and promote vesicle rupture. Our analyses evidence the gradual decrease of the main phase transition temperature upon increasing IL concentration, reflecting increased disorder by weakening of lipid chain interactions. The degree of rupture is significant for ILs with long hydrophobic cation chains and large hydrophobic anions whose behavior is reminiscent of that of antimicrobial peptides. PMID:27684947

  15. Ionic liquids modified graphene oxide composites: a high efficient adsorbent for phthalates from aqueous solution

    Science.gov (United States)

    Zhou, Xinguang; Zhang, Yinglu; Huang, Zuteng; Lu, Dingkun; Zhu, Anwei; Shi, Guoyue

    2016-12-01

    In 2015, more than 30% of erasers were found to contain a PAE content that exceeded the 0.1% limit established by the Quality and Technology Supervision Bureau of Jiangsu Province in China. Thus, strengthening the supervision and regulation of the PAE content in foods and supplies, in particular, remains necessary. Graphene oxide (GO) and its composites have drawn great interests as promising adsorbents for polar and nonpolar compounds. However, GO-based adsorbents are typically restricted by the difficult separation after treatment because of the high pressure in filtration and low density in centrifugation. Herein, a series of novel ionic liquids modified graphene oxide composites (GO-ILs) were prepared as adsorbents for phthalates (PAEs) in eraser samples, which overcame the conventional drawbacks. These novel composites have a combination of the high surface area of graphene oxide and the tunability of the ionic liquids. It is expected that the GO-ILs composites can be used as efficient adsorbents for PAEs from aqueous solution. This work also demonstrated a new technique for GO-based materials applied in sample preparation.

  16. Extraction of Co(II) from aqueous solution using emulsion liquid membrane.

    Science.gov (United States)

    Gasser, M S; El-Hefny, N E; Daoud, J A

    2008-03-01

    The extraction equilibrium of Co(II) from thiocyanate medium by CYANEX 923 (mixture of straight chain alkylated phosphine oxides) in cyclohexane was studied. The stoichiometry of the extraction reaction was postulated based on slope analysis method and the extraction constant Kex was calculated. The stripping percentage of Co(II) with sulphuric acid from the loaded CYANEX 923 was found to increase with the increase in acid concentration. The extraction of Co(II) from aqueous thiocyanate medium into emulsion liquid membrane using CYANEX 923 extractant was also studied. The influence of different parameters such as stirring speed, surfactant concentration, pH of the extractant phase, carrier concentration, internal phase stripping acid concentration, initial Co(II) concentration as well as temperature on the emulsion stability were investigated. The applicability of the emulsion liquid membrane (ELM) process using CYANEX 923 as extractant and SPAN 80 as surfactant for the removal and the concentration of Co(II) from thiocyanate solution was investigated. The results show that it is possible to recover 95% of cobalt in the inner phase after 10 min of contacting time with a concentration factor of 5.

  17. Liquid Phase Micro-Extraction of Linear Alkylbenzene Sulfonate Anionic Surfactants in Aqueous Samples

    Directory of Open Access Journals (Sweden)

    Jan Åke Jönsson

    2011-10-01

    Full Text Available Hollow fiber liquid phase micro-extraction (LPME of linear alkylbenzene sulfonates (LAS from aqueous samples was studied. Ion pair extraction of C10, C11, C12 and C13 homologues was facilitated with trihexylamine as ion-pairing agent, using di-n-hexylether as solvent for the supported liquid membrane (SLM. Effects of extraction time, acceptor buffer concentration, stirring speed, sample volume, NaCl and humic acids were studied. At 10–50 µg L−1 linear R2-coefficients were 0.99 for C10 and C11 and 0.96 for C12. RSD was typically ~15%. Three observations were especially made. Firstly, LPME for these analytes was unusually slow with maximum enrichment observed after 15–24 h (depending on sample volume. Secondly, the enrichment depended on LAS sample concentration with 35–150 times enrichment below ~150 µg L−1 and 1850–4400 times enrichment at 1 mg L−1. Thirdly, lower homologues were enriched more than higher homologues at low sample concentrations, with reversed conditions at higher concentrations. These observations may be due to the fact that LAS and the amine counter ion themselves influence the mass transfer at the water-SLM interface. The observations on LPME of LAS may aid in LPME application to other compounds with surfactant properties or in surfactant enhanced membrane extraction of other compounds.

  18. Enhanced tunability afforded by aqueous biphasic systems formed by fluorinated ionic liquids and carbohydrates†

    Science.gov (United States)

    Boal-Palheiros, Isabel; Pereiro, Ana B.; Rebelo, Luís Paulo N.; Freire, Mara G.

    2016-01-01

    This work unveils the formation of novel aqueous biphasic systems (ABS) formed by perfluoroalkylsulfonate-based ionic liquids (ILs) and a large number of carbohydrates (monosaccharides, disaccharides and polyols) aiming at establishing more benign alternatives to the salts commonly used. The respective ternary phase diagrams were determined at 298 K. The aptitude of the carbohydrates to induce phase separation closely follows their hydration capability, while the length of the IL cation/anion fluorinated chain also plays a crucial role. Finally, these systems were investigated as liquid–liquid extraction strategies for four food dyes. Single-step extraction efficiencies for the carbohydrate-rich phase up to 94% were obtained. Remarkably and contrarily to the most investigated IL-salt ABS, most dyes preferentially migrate for the most hydrophilic and biocompatible carbohydrate-rich phase – an outstanding advantage when envisaging the products recovery and further use. On the other hand, more hydrophobic dyes preferentially partition to the IL-rich phase, disclosing therefore these novel systems as highly amenable to be tuned by the proper choice of the phase-forming components. PMID:27667966

  19. Drag-Reducing Agent for Aqueous Liquid Flowing in Turbulent Mode through Pipelines

    Directory of Open Access Journals (Sweden)

    Zainab Y. Shnain

    2014-06-01

    Full Text Available In this study, mucilage was extracted from Malabar spinach and tested for drag-reducing properties in aqueous liquids flowing through pipelines. Friction produced by liquids flowing in turbulent mode through pipelines increase power consumption. Drag-reducing agents (DRA such as polymers, suspended solids and surfactants are used to reduce power losses. There is a demand for natural, biodegradable DRA and mucilage is emerging as an attractive alternative to conventional DRAs. Literature review revealed that very little research has been done on the drag-reducing properties of this mucilage and there is an opportunity to explore the potential applications of mucilage from Malabar spinach. An experimental piping rig was used to study the DR properties of the mucilage on water under the effect of varying pipe dimensions and mucilage concentrations. It is shown that these additives can dramatically reduce friction drag provided that the flow is occurring under turbulent conditions. Experimental results also show that DR increases when the mucilage concentration increases.

  20. Liquid phase micro-extraction of linear alkylbenzene sulfonate anionic surfactants in aqueous samples.

    Science.gov (United States)

    Larsson, Niklas; Otrembska, Paulina; Villar, Mercedes; Jönsson, Jan Åke

    2011-10-13

    Hollow fiber liquid phase micro-extraction (LPME) of linear alkylbenzene sulfonates (LAS) from aqueous samples was studied. Ion pair extraction of C10, C11, C12 and C13 homologues was facilitated with trihexylamine as ion-pairing agent, using di-n-hexylether as solvent for the supported liquid membrane (SLM). Effects of extraction time, acceptor buffer concentration, stirring speed, sample volume, NaCl and humic acids were studied. At 10-50 µg L-1 linear R2-coefficients were 0.99 for C10 and C11 and 0.96 for C12. RSD was typically ~15%. Three observations were especially made. Firstly, LPME for these analytes was unusually slow with maximum enrichment observed after 15-24 h (depending on sample volume). Secondly, the enrichment depended on LAS sample concentration with 35-150 times enrichment below ~150 µg L-1 and 1850-4400 times enrichment at 1 mg L-1. Thirdly, lower homologues were enriched more than higher homologues at low sample concentrations, with reversed conditions at higher concentrations. These observations may be due to the fact that LAS and the amine counter ion themselves influence the mass transfer at the water-SLM interface. The observations on LPME of LAS may aid in LPME application to other compounds with surfactant properties or in surfactant enhanced membrane extraction of other compounds.

  1. Lignocellulosic-derived modified agricultural waste: development, characterisation and implementation in sequestering pyridine from aqueous solutions.

    Science.gov (United States)

    Ahmed, Md Juned K; Ahmaruzzaman, M; Reza, Ruhul A

    2014-08-15

    The development and characterisation of modified agricultural waste (MAW) by H3PO4 activation is addressed in this study for sequestering pyridine from aqueous solutions. The adsorbent is characterised by carbon, hydrogen and nitrogen content of 55.53%, 3.28% and 0.98% respectively. The adsorbent also shows acidic (carboxylic, lactonic, phenolic groups) and basic carbon surface functionalities, functional groups viz. hydroxyl, carboxylic acid and bounded water molecules, BET surface area of 1254.67 m(2) g(-1), heterogeneous surface morphology and graphite like XRD patterns. Adsorption of pyridine is executed to evaluate the adsorptive uptake in batch (q(e)=107.18 mg g(-1)) as well as in column system (q(e)=140.94 mg g(-1)). The adsorption process followed the pseudo-second-order kinetics with the Langmuir isotherm best representing the equilibrium adsorption data. The thermodynamic parameters (ΔH(o)=9.39 kJ mol(-1), ΔG(o)=-5.99 kJ mol(-1), ΔS(o)=50.76 J K(-1) mol(-1)) confirm the endothermic and spontaneous nature of the adsorption process with increase in randomness at solid/solution interface. The adsorption mechanism is governed by electrostatic and π-π dispersive interactions as well as by a two stage diffusion phenomena. Thermally regenerated spent MAW exhibited better adsorption efficiency for five adsorption-desorption cycles than chemically regenerated. The low-cost of MAW (USD 10.714 per kg) and favourable adsorption parameters justifies its use in the adsorptive removal of pyridine.

  2. Comparison of air-agitated liquid-liquid microextraction technique and conventional dispersive liquid-liquid micro-extraction for determination of triazole pesticides in aqueous samples by gas chromatography with flame ionization detection.

    Science.gov (United States)

    Farajzadeh, Mir Ali; Mogaddam, Mohammad Reza Afshar; Aghdam, Abdollah Abdollahi

    2013-07-26

    Two micro-extraction methods, air-agitated liquid-liquid microextraction (AALLME) and dispersive liquid-liquid microextraction (DLLME), have been compared with each other by applying them for the analysis of five triazole pesticides (penconazole, hexaconazole, diniconazole, tebuconazole and triticonazole) in aqueous samples by gas chromatography with flame ionization detection (GC-FID). In the AALLME method, which excludes any disperser solvent, much less volume of organic solvent is used. In order to form fine and dispersed organic droplets in the aqueous phase, the mixture of aqueous sample solution and extraction solvent is repeatedly aspirated and dispensed with a syringe. In the DLLME method, an appropriate mixture of extraction solvent and disperser solvent is rapidly injected by a syringe into the aqueous sample. Effect of the pertinent experimental factors on DLLME (i.e. identity and volume of the extraction and disperser solvents and ionic strength) and on AALLME (identity and volume of the extraction solvent, number of agitations, and ionic strength) were investigated. Under optimal conditions, limits of detection for the five target pesticides obtained by AALLME-GC-FID and DLLME-GC-FID ranged from 0.20 to 1.1ngmL(-1) and 1.9 to 5.9ngmL(-1), respectively. The relative standard deviations (RSDs, n=5) were in the range of 1-4% and 3-5% with the enrichment factors of 449-504 and 79-143 for AALLME-GC-FID and DLLME-GC-FID, respectively. Both of the compared methods are simple, fast, efficient, inexpensive and can be applied to the analysis of the five pesticides in different aqueous samples in which penconazole and hexaconazole were found. For spiked samples, the recoveries were in the ranges of 92-105%, and 92-104% for AALLME and DLLME, respectively.

  3. Novel Solvent for the Simultaneous recovery of Radioactive Nuclides from Liquid Radioactive Wastes

    Energy Technology Data Exchange (ETDEWEB)

    Romanovskiy, Valeriy Nicholiavich; Smirnov, Lgor V.; Babain, Vasiliy A.; Todd, Terry A.; Brewer, Ken N.

    1999-10-07

    The present invention relates to solvents, and methods, for selectively extracting and recovering radionuclides, especially cesium and strontium, rare earths and actinides from liquid radioactive wastes. More specifically, the invention relates to extracting agent solvent compositions comprising complex organoboron compounds, substituted polyethylene glycols, and neutral organophosphorus compounds in a diluent. The preferred solvent comprises a chlorinated cobalt dicarbollide, diphenyl-dibutylmethylenecarbamoylphosphine oxide, PEG-400, and a diluent of phenylpolyfluoroalkyl sulfone. The invention also provides a method of using the invention extracting agents to recover cesium, strontium, rare earths and actinides from liquid radioactive waste.

  4. Validated Test Method 5030C: Purge-and-Trap for Aqueous Samples

    Science.gov (United States)

    This method describes a purge-and-trap procedure for the analysis of volatile organic compoundsin aqueous samples & water miscible liquid samples. It also describes the analysis of high concentration soil and waste sample extracts prepared in Method 5035.

  5. Development of Advanced Electrochemical Emission Spectroscopy for Monitoring Corrosion in Simulated DOE Liquid Waste

    Energy Technology Data Exchange (ETDEWEB)

    MacDonal, Digby D.; Marx, Brian M.; Ahn, Sejin; Ruiz, Julio de; Soundararajan, Balaji; Smith, Morgan; Coulson, Wendy

    2005-06-15

    Various forms of general and localized corrosion represent principal threats to the integrity of DOE liquid waste storage tanks. These tanks, which are of a single wall or double wall design, depending upon their age, are fabricated from welded carbon steel and contain a complex waste-form comprised of NaOH and NaNO3, along with trace amounts of phosphate, sulfate, carbonate, and chloride. Because waste leakage can have a profound environmental impact, considerable interest exists in predicting the accumulation of corrosion damage, so as to more effectively schedule maintenance and repair.

  6. Evaluation of transport properties of nanofiltration membranes exposed to radioactive liquid waste

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Elizabeth E.M.; Barbosa, Celina C.R.; Bastos, Edna T.R., E-mail: eemo@ien.gov.br [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeira, RJ (Brazil); Afonso, Julio C., E-mail: Julio@iq.ufrj.br [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Inst. de Quimica. Dept. de Quimica Analitica

    2011-07-01

    The application of membrane separation processes (PSM) for treatment of radioactive waste requires the selection of a suitable membrane for the treatment of waste, as the membrane will be directly exposed to the radioactive liquid waste, and also exposed to ionizing radiation. The nanofiltration membrane is most suitable for treatment of radioactive waste, since it has high rejection of multivalent ions. Usually the membranes are made of polymers and depending on the composition of the waste, type and dose of radiation absorbed may be changes in the structure of the membrane, resulting in loss of its transport properties. We tested two commercial nanofiltration membranes: NF and SW Dow/Filmtec. The waste liquid used was obtained in the process of conversion of uranium hexafluoride gas to solid uranium dioxide, known as 'carbonated water'. The membranes were characterized as their transport properties (hydraulic permeability, permeate flux and salt rejection) before and after their immersion in the waste for 24 hours. The surface of the membranes was also evaluated by SEM and FTIR. It was observed that in both the porosity of the membrane selective layer was altered, but not the membrane surface charge, which is responsible for the selectivity of the membrane. The NF membranes and SW showed uranium ion rejection of 64% and 55% respectively. (author)

  7. Municipal Solid Waste (MSW) to Liquid Fuels Synthesis, Volume 1: Availability of Feedstock and Technology

    Energy Technology Data Exchange (ETDEWEB)

    Valkenburt, Corinne; Walton, Christie W.; Thompson, Becky L.; Gerber, Mark A.; Jones, Susanne B.; Stevens, Don J.

    2008-12-01

    This report investigated the potential of using municipal solid waste (MSW) to make synthesis gas (syngas) suitable for production of liquid fuels. Issues examined include: • MSW physical and chemical properties affecting its suitability as a gasifier feedstock and for liquid fuels synthesis • expected process scale required for favorable economics • the availability of MSW in quantities sufficient to meet process scale requirements • the state-of-the-art of MSW gasification technology.

  8. ASSESSING THE LEACHING BEHAVIOR OF METALS FROM A MINERAL PROCESSING WASTE AS A FUNCTION OF LIQUID TO SOLID RATIO

    Science.gov (United States)

    A mineral processing waste was used to study the effect of liquid to solid ratio (L/S) on the leaching behavior of metals. Leaching tests in the form of column and batch studies were carried out to investigate liquid to solid ratios ranging from 0.7 to 50. Although the waste pa...

  9. Determination of tamsulosin in human aqueous humor and serum by liquid chromatography-electrospray ionization tandem mass spectrometry.

    Science.gov (United States)

    Keski-Rahkonen, Pekka; Pärssinen, Olavi; Leppänen, Esa; Mauriala, Timo; Lehtonen, Marko; Auriola, Seppo

    2007-01-17

    A simple, sensitive and selective LC-MS/MS method was developed for the determination of tamsulosin in human aqueous humor and serum to study the recently reported eye-related adverse effects of this alpha(1)-blocker drug. Aqueous humor samples were analyzed by direct injection, after addition of the internal standard, labetalol. Liquid-liquid extraction with ethyl acetate was used for serum sample preparation. The chromatographic separation was performed on a reversed phase column by gradient elution with acetonitrile -0.1% formic acid at a flow-rate of 0.2 ml/min. Detection and quantification of the analytes were carried out with a linear ion trap mass spectrometer, using positive electrospray ionization (ESI) and multiple reaction monitoring (MRM). The limit of quantification was 0.1 ng/ml for both aqueous humor and serum samples and linearity was obtained over the concentration ranges of 0.1-4.7 ng/ml and 0.1-19.3 ng/ml for aqueous humor and serum samples, respectively. Acceptable accuracy and precision were obtained for concentrations within the standard curve ranges. The method has been used for the determination of tamsulosin in aqueous humor and serum samples from patients that were on tamsulosin medication and underwent cataract surgery.

  10. Removal of Pb(II) ions from aqueous solution using activated tea waste: Adsorption on a fixed-bed column.

    Science.gov (United States)

    Mondal, M K

    2009-08-01

    An inexpensive and effective adsorbent was developed from waste tea leaves for the dynamic uptake of Pb(II). Characterization of the adsorbents showed a clear change between physico-chemical properties of activated tea waste and simply tea waste. The purpose of this work was to evaluate the potential of activated tea waste in continuous flow removal of Pb(II) ions from synthetic aqueous effluents. The performance of the system was evaluated to assess the effect of various process variables, viz., of bed height, hydraulic loading rate and initial feed concentration on breakthrough time and adsorption capacity. The shape of the breakthrough curves was determined for the adsorption of Pb(II) by varying different operating parameters like hydraulic loading rate (2.3-9.17m(3)/hm(2)), bed height (0.3-0.5m) and feed concentration (2-10mg/l). An attempt has also been made to model the data generated from column studies using the empirical relationship based on the Bohart-Adams model. There was an acceptable degree of agreement between the data for breakthrough time calculated from the Bohart-Adams model and the present experimental study with average absolute deviation of less than 5.0%. The activated tea waste in this study showed very good promise as compared with the other adsorbents available in the literature. The adsorbent could be suitable for repeated use (for more than four cycles) without noticeable loss of capacity.

  11. Potential Development of Liquid Smoke from Oil Palm Solid Waste as Biofungicides

    Directory of Open Access Journals (Sweden)

    Asri Gani

    2014-05-01

    Full Text Available This research investigated the potential utilization of solid waste from palm oil industry for liquid smoke production in Aceh Province, Indonesia. The liquid smoke can be applied as bio fungicides in agricultural field. Preliminary experiment on the use of liquid smoke as fungicide at Colletotrichum capsisi fungus which causes anthracnose disease on red pepper was also conducted. The survey on the existing potential/availability of palm oil mill in Aceh shows that there are 30 palm oil mills in eight districts with a total of production capacity 1020 ton/hour. Assuming that 10% of palm oil kernel shells are pyrolized into liquid smoke, Aceh province could produce about 23,868 ton of liquid smoke per year. The preliminary test result towards Colletotrichum capsisi fungus shows that the liquid smoke can be used as fungicides.

  12. Biochemical process of low level radioactive liquid simulation waste containing detergent

    Energy Technology Data Exchange (ETDEWEB)

    Kundari, Noor Anis, E-mail: nooranis@batan.go.id; Putra, Sugili; Mukaromah, Umi [Sekolah Tinggi Teknologi Nuklir – Badan Tenaga Nuklir Nasional Jl. Babarsari P.O. BOX 6101 YKBB Yogyakarta 55281 Telp : (0274) 48085, 489716, Fax : (0274) 489715 (Indonesia)

    2015-12-29

    Research of biochemical process of low level radioactive liquid waste containing detergent has been done. Thse organic liquid wastes are generated in nuclear facilities such as from laundry. The wastes that are cotegorized as hazard and poison materials are also radioactive. It must be treated properly by detoxification of the hazard and decontamination of the radionuclides to ensure that the disposal of the waste meets the requirement of standard quality of water. This research was intended to determine decontamination factor and separation efficiensies, its kinetics law, and to produce a supernatant that ensured the environmental quality standard. The radioactive element in the waste was thorium with activity of 5.10{sup −5} Ci/m{sup 3}. The radioactive liquid waste which were generated in simulation plant contains detergents that was further processed by aerobic biochemical process using SGB 103 bacteria in a batch reactor equipped with aerators. Two different concentration of samples were processed and analyzed for 212 hours and 183 hours respectively at a room temperature. The product of this process is a liquid phase called as supernatant and solid phase material called sludge. The chemical oxygen demand (COD), biological oxygen demand (BOD), suspended solid (SS), and its alpha activity were analyzed. The results show that the decontamination factor and the separation efficiency of the lower concentration samples are higher compared to the samples with high concentration. Regarding the decontamination factor, the result for 212 hours processing of waste with detergent concentration of 1.496 g/L was 3.496 times, whereas at the detergent concentration of 0.748 g/L was 15.305 times for 183 hours processing. In case of the separation efficiency, the results for both samples were 71.396% and 93.465% respectively. The Bacterial growth kinetics equation follow Monod’s model and the decreasing of COD and BOD were first order with the rate constant of 0

  13. Biochemical process of low level radioactive liquid simulation waste containing detergent

    Science.gov (United States)

    Kundari, Noor Anis; Putra, Sugili; Mukaromah, Umi

    2015-12-01

    Research of biochemical process of low level radioactive liquid waste containing detergent has been done. Thse organic liquid wastes are generated in nuclear facilities such as from laundry. The wastes that are cotegorized as hazard and poison materials are also radioactive. It must be treated properly by detoxification of the hazard and decontamination of the radionuclides to ensure that the disposal of the waste meets the requirement of standard quality of water. This research was intended to determine decontamination factor and separation efficiensies, its kinetics law, and to produce a supernatant that ensured the environmental quality standard. The radioactive element in the waste was thorium with activity of 5.10-5 Ci/m3. The radioactive liquid waste which were generated in simulation plant contains detergents that was further processed by aerobic biochemical process using SGB 103 bacteria in a batch reactor equipped with aerators. Two different concentration of samples were processed and analyzed for 212 hours and 183 hours respectively at a room temperature. The product of this process is a liquid phase called as supernatant and solid phase material called sludge. The chemical oxygen demand (COD), biological oxygen demand (BOD), suspended solid (SS), and its alpha activity were analyzed. The results show that the decontamination factor and the separation efficiency of the lower concentration samples are higher compared to the samples with high concentration. Regarding the decontamination factor, the result for 212 hours processing of waste with detergent concentration of 1.496 g/L was 3.496 times, whereas at the detergent concentration of 0.748 g/L was 15.305 times for 183 hours processing. In case of the separation efficiency, the results for both samples were 71.396% and 93.465% respectively. The Bacterial growth kinetics equation follow Monod's model and the decreasing of COD and BOD were first order with the rate constant of 0.01 hour-1.

  14. Utilization of TiO2 deposited on glass plates for removal of metals from aqueous wastes

    Science.gov (United States)

    Hilmi; Luong; Nguyen

    1999-02-01

    Glass plates coated with TiO2 were used in a photocatalytic process to collect mercury, lead, copper and cadmium from aqueous solutions containing individual metals and mixtures. Stripping voltammetry, verified to achieve 1-10 ppb detection limits, was used to show that individual metals at concentrations of 1000 to 5200 ppb were reduced to undetectable levels in 3 to 55 min. Capillary electrophoresis (CE) with 8-hydroxyquinoline-5-sulfonic acid as complexing agent was used when appropriate, since it could quantitate all four metals under study in one run although it was less sensitive. It was demonstrated that 100 mL solutions containing 10 ppm of each of the four metals could be treated with a 10 cm2 TiO2-coated plate to leave undetectable metal concentrations in one hour. Stripping voltammetry using carbon electrodes coated with mercury films was estimated to generate daily about 1.1 L of aqueous waste containing 0.1 ppm of each metal. The results indicate the feasibility of assembling an apparatus capable of treating the waste generated by stripping voltammetry to render the latter suitable for routine on-site analyses without environmental concern. Data were also obtained to show the effectiveness in treating silver containing solutions, indicating suitability of the photocatalytic process in treating photographic processing wastes.

  15. Microbial consortium role in processing liquid waste of vegetables in Keputran Market Surabaya as organic liquid fertilizer ferti-plus

    Science.gov (United States)

    Rizqi, Fauziah; Supriyanto, Agus; Lestari, Intan; Lita Indri D., L.; Elmi Irmayanti, A.; Rahmaniyah, Fadilatur

    2016-03-01

    Many activities in this market is directly proportional to increase production of vegetables waste, especially surabaya. Therefore, in this study aims to utilize liquid waste of vegetables into liquid organic fertilizer by mixing microbial consorsium. The microbial consorsium consist of Azotobacter chrococcum, Azospirillum brasilense, Rhizobium leguminosarum, Bacillus subtilis, Bacillus megaterium, Pseudomonas putida, and Pseudomonas fluorescens. Ttreatment of microbial concentrations (5%, 10%, 15%) and the length of the incubation period (7 days, 14 days, 21 days) used in this research. The parameters used are: C/N ratio, levels of CNP, and BOD value. This study uses a standard organic fertilizer value according SNI19-7030-2004, The results show the value of C/N ratio comply with the ISO standards. C levels showed an increase during the incubation period but not compare with standards. N levels that compare with standards are microbial treatment in all group concentration except control group with an incubation period of 21 days is > 7. P levels compare with the existing standards in the group of microbe concentration of 10% and 15% during the incubation period. The value of the initial BOD liquid waste of vegetable is 790.25 mg / L, this value indicates that the waste should not go into the water body. Accordingly, the results of this study can not be used as a liquid organic fertilizer, but potentially if it is used as a natural career or build natural soil. The Building natural soil is defined as the natural ingredients that can be used to improve soil properties.

  16. Investigation on the characteristics of liquid wastes depending on their generation sources and study on optimum treatment method

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Sang Guk; Kim, Dong Chan; Shin, Dae Hyun; Son, Seung Geun; Roh, Nam Sun; Woo, Je Kyung [Korea Inst. of Energy Research, Taejon (Korea, Republic of)

    1995-12-01

    The major research contents conducted this year are as follows: (1) environmental regulation with respect to the treatment of the liquid waste in the U.S.A., (2) the present status of the generation and treatment of liquid wastes for large producers(>1,000 ton/year), (3) analysis for heating value element, heavy metal content, halogenated species on collected samples, (4) investigation on estimation method of energy recovery rate from liquid waste, (5) design of a lab. scale reactor which could be capable of conducting thermal decomposition test with small quantity of sample. In this study, present status of liquid waste generation and treatment is investigated, and thermal decomposition characteristics are studied using a lab. scale thermal reactor. The purpose of this research is to divide liquid waste into groups and to present best treatment method for their each group. (author). 24 refs., 21 figs., 23 tabs.

  17. Thermodynamic studies of ionic hydration and interactions for amino acid ionic liquids in aqueous solutions at 298.15 K.

    Science.gov (United States)

    Dagade, Dilip H; Madkar, Kavita R; Shinde, Sandeep P; Barge, Seema S

    2013-01-31

    Amino acid ionic liquids are a special class of ionic liquids due to their unique acid-base behavior, biological significance, and applications in different fields such as templates in synthetic chemistry, stabilizers for biological macromolecules, etc. The physicochemical properties of these ionic liquids can easily be altered by making the different combinations of amino acids as anion along with possible cation modification which makes amino acid ionic liquids more suitable to understand the different kinds of molecular and ionic interactions with sufficient depth so that they can provide fruitful information for a molecular level understanding of more complicated biological processes. In this context, volumetric and osmotic coefficient measurements for aqueous solutions containing 1-ethyl-3-methylimidazolium ([Emim]) based amino acid ionic liquids of glycine, alanine, valine, leucine, and isoleucine are reported at 298.15 K. From experimental osmotic coefficient data, mean molal activity coefficients of ionic liquids were estimated and analyzed using the Debye-Hückel and Pitzer models. The hydration numbers of ionic liquids in aqueous solutions were obtained using activity data. Pitzer ion interaction parameters are estimated and compared with other electrolytes reported in the literature. The nonelectrolyte contribution to the aqueous solutions containing ionic liquids was studied by calculating the osmotic second virial coefficient through an application of the McMillan-Mayer theory of solution. It has been found that the second osmotic virial coefficient which includes volume effects correlates linearly with the Pitzer ion interaction parameter estimated independently from osmotic data as well as the hydrophobicity of ionic liquids. The enthalpy-entropy compensation effect, explained using the Starikov-Nordén model of enthalpy-entropy compensation, and partial molar entropy analysis for aqueous [Emim][Gly] solutions are made by using experimental Gibb

  18. Investigation into the temporal stability of aqueous standard solutions of psilocin and psilocybin using high performance liquid chromatography.

    Science.gov (United States)

    Anastos, N; Barnett, N W; Pfeffer, F M; Lewis, S W

    2006-01-01

    This paper reports an investigation into the temporal stability of aqueous solutions of psilocin and psilocybin reference drug standards over a period of fourteen days. This study was performed using high performance liquid chromatography utilising a (95:5% v/v) methanol: 10 mM ammonium formate, pH 3.5 mobile phase and absorption detection at 269 nm. It was found that the exclusion of light significantly prolonged the useful life of standards, with aqueous solutions of both psilocin and psilocybin being stable over a period of seven days.

  19. Chromium liquid waste inertization in an inorganic alkali activated matrix: Leaching and NMR multinuclear approach

    Energy Technology Data Exchange (ETDEWEB)

    Ponzoni, Chiara, E-mail: chiara.ponzoni@unimore.it [University of Modena and Reggio Emilia, Department of Engineering “Enzo Ferrari”, Modena (Italy); Lancellotti, Isabella; Barbieri, Luisa [University of Modena and Reggio Emilia, Department of Engineering “Enzo Ferrari”, Modena (Italy); Spinella, Alberto; Saladino, Maria Luisa [University of Palermo CGA-UniNetLab, Palermo (Italy); Martino, Delia Chillura [University of Palermo, Department STEBICEF, Palermo (Italy); Caponetti, Eugenio [University of Palermo CGA-UniNetLab, Palermo (Italy); University of Palermo, Department STEBICEF, Palermo (Italy); Armetta, Francesco [University of Palermo, Department STEBICEF, Palermo (Italy); Leonelli, Cristina [University of Modena and Reggio Emilia, Department of Engineering “Enzo Ferrari”, Modena (Italy)

    2015-04-09

    Highlights: • Inertization of chromium liquid waste in aluminosilicate matrix. • Water less inertization technique exploiting the waste water content. • Liquid waste inertization without drying step. • Long term stabilization study through leaching test. • SEM analysis and {sup 29}Si and {sup 27}Al MAS NMR in relation with long curing time. - Abstract: A class of inorganic binders, also known as geopolymers, can be obtained by alkali activation of aluminosilicate powders at room temperature. The process is affected by many parameters (curing time, curing temperature, relative humidity etc.) and leads to a resistant matrix usable for inertization of hazardous waste. In this study an industrial liquid waste containing a high amount of chromium (≈2.3 wt%) in the form of metalorganic salts is inertized into a metakaolin based geopolymer matrix. One of the innovative aspects is the exploitation of the water contained in the waste for the geopolymerization process. This avoided any drying treatment, a common step in the management of liquid hazardous waste. The evolution of the process - from the precursor dissolution to the final geopolymer matrix hardening - of different geopolymers containing a waste amount ranging from 3 to 20% wt and their capability to inertize chromium cations were studied by: i) the leaching tests, according to the EN 12,457 regulation, at different curing times (15, 28, 90 and 540 days) monitoring releases of chromium ions (Cr(III) and Cr(VI)) and the cations constituting the aluminosilicate matrix (Na, Si, Al); ii) the humidity variation for different curing times (15 and 540 days); iii) SEM characterization at different curing times (28 and 540 days); iv) the trend of the solution conductivity and pH during the leaching test; v) the characterization of the short-range ordering in terms of T−O−T bonds (where T is Al or Si) by {sup 29}Si and {sup 27}Al solid state magic-angle spinning nuclear magnetic resonance (ss MAS NMR) for

  20. A Comparative Study of Cellulose Agricultural Wastes (Almond Shell, Pistachio Shell, Walnut Shell, Tea Waste And Orange Peel for Adsorption of Violet B Dye from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Saeedeh Hashemian

    2014-12-01

    Full Text Available Adsorption of violet B azo dye from aqueous solutions was studied by different cellulose agriculturalwaste materials (almond shell (AS, pistachio shell (PS, walnut shell (WS, Tea waste (TW and orange peel (OP. Cellulose agricultural waste sorbents characterized by FTIR and SEM methods. The effects of different parameters such as contact time, pH, adsorbent dosage and initial dye concentration were studied.Maximum removal of dye was obtained at contact time of 90 min and pH 11.The adsorption of violet B was fitted by pseudo-second-order kinetic model.The Langmuir isotherm model was better fitted than Freundlichmodel. The results showed that the adsorption efficiency of violet B by cellulose agricultural waste materials is as followed: Almond shell > Orange peel > Pistachio shell > Tea waste> Walnut shell.The maximum adsorption capacity was obtained 96, 82, 71.4, 55.5 and 48.7 mg g−1 for AS, OP, PS, TW and WS, respectively.

  1. (Liquid + liquid) and (liquid + solid) equilibrium of aqueous two-phase systems containing poly ethylene glycol di-methyl ether 2000 and di-sodium hydrogen phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Zafarani-Moattar, Mohammed Taghi, E-mail: zafarani47@yahoo.co [Physical Chemistry Department, University of Tabriz, Tabriz 51664 (Iran, Islamic Republic of); Nasiri, Saeed [Physical Chemistry Department, University of Tabriz, Tabriz 51664 (Iran, Islamic Republic of)

    2010-09-15

    (Liquid + liquid) equilibrium (LLE) for the {l_brace}poly ethylene glycol di-methyl ether 2000 (PEGDME{sub 2000}) + Na{sub 2}HPO{sub 4} + H{sub 2}O{r_brace} system have been determined experimentally at T = (298.15, 308.15, 313.15, and 318.15) K. The effects of temperature on the binodals and tie-lines for the investigated aqueous two-phase system (ATPS) have been studied. An empirical non-linear expression developed by Merchuk was used for reproducing the experimental binodal data. In this work, the three fitting parameters of the Merchuk equation were obtained with the temperature dependence expressed in the linear form with (T - T{sub 0}) K as a variable. Furthermore, the modified local composition segment-based NRTL and Wilson models and also osmotic virial equation were used to describe the LLE data of the studied system. Also, the effects of the type of salt on LLE are discussed. In addition, the effects of end groups of the polymers PEGDME{sub 2000} and poly ethylene glycol 2000 on phase forming ability were studied. The complete phase diagram for the poly ethylene {l_brace}glycol di-methyl ether 2000 (PEGDME{sub 2000}) + Na{sub 2}HPO{sub 4} + H{sub 2}O{r_brace} system has also been determined at T = 298.15 K.

  2. Effective removal of tetracycline from aqueous solution using activated carbon prepared from tomato (Lycopersicon esculentum Mill.) industrial processing waste.

    Science.gov (United States)

    Sayğılı, Hasan; Güzel, Fuat

    2016-09-01

    Activated carbon (TAC) prepared under optimized conditions with ZnCl2 activation from a new precursor; tomato industrial processing waste (TW), was applied as an adsorbent to remove tetracycline (TC) from aqueous solution. The factors (TAC dosage, initial TC concentration, contact time, ionic strength and solution temperature) affecting the adsorption process were examined at natural pH (5.7) of TAC-TC system in aqueous solution. Kinetic data was found to be best complied by the pseudo-second order model. The isotherm analysis indicated that the equilibrium data could be represented by the Langmuir model. The maximum adsorption capacity was identified as 500.0mgg(-1) at 308K.

  3. Radioactive liquid wastes discharged to ground in the 200 Areas during 1978

    Energy Technology Data Exchange (ETDEWEB)

    Anderson, J. D.; Poremba, B. E.

    1979-03-26

    This document is issued quarterly for the purpose of summarizing the radioactive liquid wastes that have been discharged to the ground in the 200 Areas. In addition to data for 1978, cumulative data since plant startup are presented. Also, in this document is a listing of decayed activity to the various plant sites.

  4. Annual Treatment Operation Report of Radioactive Liquid Waste in Temporary Storage in 2015

    Institute of Scientific and Technical Information of China (English)

    LI; Wei; DU; Guang-fei; WANG; Jian-xin; SHAO; Yan-jiang; DU; Hong-ming

    2015-01-01

    This project was officially approved in 2011.2015was the 4th running year that to treat the radioactive liquid waste in the temporary storage.According to the project plan,all work had been completed.The financial accounts and audit had been finished.The main task included the cement

  5. Annual Treatment Operation Report of Radioactive Liquid Waste in Temporary Storage

    Institute of Scientific and Technical Information of China (English)

    DU; Hong-ming; LIU; Fu-guo; WANG; Jian-xin; DU; Guang-fei; LI; Wei

    2013-01-01

    This project got the official reply formally in 2011.2013 was the second running year that to treat the radioactive liquid waste in the temporary storage.The main task was cement solidification and evaporation treatment of the radioactive wastewater.The task of each running node had completed

  6. Bioethanol Production from Liquid Waste of Rice Flour with Batch Process

    Directory of Open Access Journals (Sweden)

    Ketut Sari Ni

    2016-01-01

    Full Text Available Liquid waste rice flour is abundant liquid wastes but it is still underutilized. So far, it is only used for process water in factory production, wastewater, and even regarded as environment pollution. Rice flour liquid waste has higher levels of glucose, starch and protein which can be used as one of ethanol producers. This study aims to assess the process of hydrolysis, fermentation, and batch distillation process, as well as to search for alternative raw materials products of bioethanol. There are three processes of making bioethanol, namely biological hydrolysis process done by using bacillus; the process of fermentation by using Saccharomyces cerevisiae (SC; and batch distillation. After the third process was done, the results were: glucose is 5% - 10% in the process of hydrolysis; ethanol content is 11% - 16% in the fermentation process; and the levels are high enough for bio-ethanol, which is 95% - 96% in the batch distillation process. So it can be concluded that the liquid waste of rice flour can be used as raw materials for the manufacture of alternative bioethanol.

  7. Application of zeolitised coal fly ashes to the depuration of liquid wastes

    Energy Technology Data Exchange (ETDEWEB)

    Emilia Otal; Luis F. Vilches; Natalia Moreno; Xavier Querol; Jose Valea; Constantino Fernandez-Pereira [Universidad de Sevilla, Seville (Spain). Dpto. Ingenieria Quimica y Ambiental, E.S. Ingenieros Industriales

    2005-08-01

    In this study, the application of some zeolitised fly ashes and synthetic zeolites to the decontamination of the leachate produced in a municipal solid waste (MSW) treatment plant and to the liquid waste from a pig farm was analyzed. Thus, the reduction of organic matter (BOD and COD), ammonium and total nitrogen, phosphorus and metals contents after a zeolite treatment was evaluated. Several synthetic zeolites were tested: some commercial zeolites and other synthetic zeolites and zeolitised ashes obtained after a coal fly ash alkaline hydrothermal process. Two forms of contact between the zeolitic material and the liquid waste were tested: in a stirred tank and in a column. In addition, other variables determined were the amount of zeolite and the residence time. The results showed that zeolites, especially zeolitised fly ash, clearly produced a strong reduction in the leachate nitrogen and phosphorus content. 14 refs., 1 fig., 9 tabs.

  8. Uptake of Pb(II) ion From Aqueous Solution Using Silk Cotton Hull Carbon: An Agricultural Waste Biomass

    OpenAIRE

    Shanmugavalli, R.; P. S. Syed Shabudeen; R. Venckatesh; K. Kadirvelu; S. Madhavakrishnan; S. Pattabhi

    2006-01-01

    Activated carbon prepared from silk cotton hull (SCH) was used for the adsorptive removal of Pb(II) ion from aqueous solution. The raw material used for the preparation of activated carbon is the waste of agricultural product; the production of this carbon is expected to be economically feasible. Parameters such as agitation time, metal ion concentration, adsorbent dose, pH and Particle size were studied. Adsorption equilibrium was reached within 80 min for 10, 20, 30 and 40mg/l of Pb(II) ion...

  9. EVALUATION OF THE REMOVAL OF ARSENIC AND CADMIUM FROM AQUEOUS SOLUTION USING NATURAL RHYOLITIC SEDIMENTS AND METALLURGICAL WASTES

    OpenAIRE

    Luis Gerardo MARTÍNEZ JARDINES; Francisco MARTÍN ROMERO; Margarita Eugenia GUTIÉRREZ RUIZ; Águeda Elena CENICEROS GÓMEZ

    2012-01-01

    The use of natural materials abundant, efficient and inexpensive for use in stabilization of contaminants is in development, so some sorbent materials for removal of Cd (II) on aqueous solutions in the range of 10-100 mg/L and for As (III) and As (V) in the range of 1-500 mg/L have been investigated. The sorbent materials studied are indigenous rhyolitic sediments and metallurgical wastes from San Luis Potosi, Mexico. Mineralogical analysis showed that rhyolitic sediments are characterized by...

  10. Milliscale Self-Integration of Megamolecule Biopolymers on a Drying Gas-Aqueous Liquid Crystalline Interface.

    Science.gov (United States)

    Okeyoshi, Kosuke; Okajima, Maiko K; Kaneko, Tatsuo

    2016-06-13

    A drying environment is always a proposition faced by dynamic living organisms using water, which are driven by biopolymer-based micro- and macrostructures. Here, we introduce a drying process for aqueous liquid crystalline (LC) solutions composed of biopolymer with extremely high molecular weight components such as polysaccharides, cytoskeletal proteins, and DNA. On controlling the mobility of the LC microdomain, the solutions showed milliscale self-integration starting from the unstable gas-LC interface during drying. In particular, we first identified giant rod-like microdomains (∼1 μm diameter and more than 20 μm length) of the mega-molecular polysaccharide, sacran, which is remarkably larger than other polysaccharides. These microdomains led to the formation of a single milliscale macrodomain on the interface. In addition, the dried polymer films on a solid substrate also revealed that such integration depends on the size of the microdomain. We envision that this simple drying method will be useful not only for understanding the biopolymer hierarchization at the macroscale level but also for preparation of surfaces with direction controllability, as seen in living organisms, for use in various fields such as diffusion, mechanics, and photonics.

  11. Infiltration characteristics of non-aqueous phase liquids in undisturbed loessal soil cores

    Institute of Scientific and Technical Information of China (English)

    WANG Yunqiang; SHAO Ming'an

    2009-01-01

    The widespread contamination of soils and aquifers by non-aqueous phase liquids (NAPL), such as crude oil, poses serious environmental and health hazards globally. Understanding the infiltration characteristics of NAPL in soil is crucial in mitigating or remediating soil contamination. The infiltration characteristics of crude and diesel oils into undisturbed loessal soil cores, collected in polymethyl methacrylate cylindrical columns, were investigated under a constant fluid head (3 cm) of either crude oil or diesel oil. The infiltration rate of both crude and diesel oils decreased exponentially as wetting depth increased with time. Soil core size and bulk density both had a significant effect on NAPL infiltration through the undisturbed soil cores; a smaller core size or a greater bulk density both reduced oil penetration to depth. Compacting soil in areas susceptible to oil spills may be an effective way to reduce contamination. The infiltration of NAPL into soil cores was spatially anisotropic and heterogeneous, thus recording the data at four points on the soil core is a good way to improve the accuracy of experimental results. Our results provided information about crude and diesel oils, rather than their components, and may have practical value for remediation of contaminated loessal soils.

  12. Gas-liquid partitioning of halogenated volatile organic compounds in aqueous cyclodextrin solutions

    Energy Technology Data Exchange (ETDEWEB)

    Ondo, Daniel; Barankova, Eva [Department of Physical Chemistry, Institute of Chemical Technology, Technicka 5, 166 28 Prague 6 (Czech Republic); Dohnal, Vladimir, E-mail: dohnalv@vscht.cz [Department of Physical Chemistry, Institute of Chemical Technology, Technicka 5, 166 28 Prague 6 (Czech Republic)

    2011-08-15

    Highlights: > Binding of halogenated VOCs with cyclodextrins examined through g-l partitioning. > Complex stabilities reflect host-guest size matching and hydrophobic interaction. > Presence of halogens in the guest molecule stabilizes the binding. > Thermodynamic origin of the binding varies greatly among the systems studied. > Results obey the guest-CD global enthalpy-entropy compensation relationship. - Abstract: Gas-liquid partitioning coefficients (K{sub GL}) were measured for halogenated volatile organic compounds (VOCs), namely 1-chlorobutane, methoxyflurane, pentafluoropropan-1-ol, heptafluorobutan-1-ol, {alpha},{alpha},{alpha}-trifluorotoluene, and toluene in aqueous solutions of natural {alpha}-, {beta}-, and {gamma}-cyclodextrins (CDs) at temperatures from (273.35 to 326.35) K employing the techniques of headspace gas chromatography and inert gas stripping. The binding constants of the 1:1 inclusion complex formation between the VOCs and CDs were evaluated from the depression of the VOCs volatility as a function of CD concentration. The host-guest size matching and the hydrophobic interaction concept were used to rationalize the observed widely different affinity of the VOC-CD pairs to form the inclusion complex. The enthalpic and entropic component of the standard Gibbs free energy of complex formation as derived from the temperature dependence of the binding constant indicate the thermodynamic origin of the binding to vary greatly among the systems studied, but follow the global enthalpy-entropy compensation relationships reported previously in the literature.

  13. Aqueous two phase system based on ionic liquid for isolation of quinine from human plasma sample.

    Science.gov (United States)

    Flieger, J; Czajkowska-Żelazko, A

    2015-01-01

    Aqueous two phase system was applied for selective extraction of quinine from human plasma. Bi-phase was constructed from ionic liquid: butyl-methyl-imidazolium chloride after addition kosmotropic salts K₃PO₄ or KH₂PO₄. Quinine was determined in plasma samples after drinking of tonic containing quinine. Determination was performed by HPLC on 5-μm Zorbax SB-CN column and eluent containing 40% acetonitrile (v/v), 20 mM phosphate buffer at pH 3 and 40 mM NaPF₆ using external standard method. The spectrophotometric detection was set λ=214 nm. Selective fluorescence detection was performed at excitation of 325 nm and emission of 375 nm. Proposed strategy provides suitable sample purification and gives extraction yields in the range of 89-106%. The determination coefficient (R(2)) has a value ≥0.997 in the range of 50-800 ng/ml quinine concentration. The limit of quantification was set at 27.9 ng/ml and the detection limit was found to be 8.4 ng/ml under fluorescence detection.

  14. Ionic Liquid-Based Non-Aqueous Electrolytes for Nickel/Metal Hydride Batteries

    Directory of Open Access Journals (Sweden)

    Tiejun Meng

    2017-02-01

    Full Text Available The voltage of an alkaline electrolyte-based battery is often limited by the narrow electrochemical stability window of water (1.23 V. As an alternative to water, ionic liquid (IL-based electrolyte has been shown to exhibit excellent proton conducting properties and a wide electrochemical stability window, and can be used in proton conducting batteries. In this study, we used IL/acid mixtures to replace the 30 wt % KOH aqueous electrolyte in nickel/metal hydride (Ni/MH batteries, and verified the proton conducting character of these mixtures through electrochemical charge/discharge experiments. Dilution of ILs with acetic acid was found to effectively increase proton conductivity. By using 2 M acetic acid in 1-ethyl-3-methylimidazolium acetate, stable charge/discharge characteristics were obtained, including low charge/discharge overpotentials, a discharge voltage plateau at ~1.2 V, a specific capacity of 161.9 mAh·g−1, and a stable cycling performance for an AB5 metal hydride anode with a (Ni,Co,Zn(OH2 cathode.

  15. Liquid-liquid-solid microextraction based on membrane-protected molecularly imprinted polymer fiber for trace analysis of triazines in complex aqueous samples.

    Science.gov (United States)

    Hu, Yuling; Wang, Yangyang; Hu, Yufei; Li, Gongke

    2009-11-20

    A novel liquid-liquid-solid microextraction (LLSME) technique based on porous membrane-protected molecularly imprinted polymer (MIP)-coated silica fiber has been developed. In this technique, a MIP-coated silica fiber was protected with a length of porous polypropylene hollow fiber membrane which was filled with water-immiscible organic phase. Subsequently the whole device was immersed into aqueous sample for extraction. The LLSME technique was a three-phase microextraction approach. The target analytes were firstly extracted from the aqueous sample through a few microliters of organic phase residing in the pores and lumen of the membrane, and were then finally extracted onto the MIP fiber. A terbutylazine MIP-coated silica fiber was adopted as an example to demonstrate the feasibility of the novel LLSME method. The extraction parameters such as the organic solvent, extraction and desorption time were investigated. Comparison of the LLSME technique was made with molecularly imprinted polymer based solid-phase microextraction (MIP-SPME) and hollow fiber membrane-based liquid-phase microextraction (HF-LPME), respectively. The LLSME, integrating the advantages of high selectivity of MIP-SPME and enrichment and sample cleanup capability of the HF-LPME into a single device, is a promising sample preparation method for complex samples. Moreover, the new technique overcomes the problem of disturbance from water when the MIP-SPME fiber was exposed directly to aqueous samples. Applications to analysis of triazine herbicides in sludge water, watermelon, milk and urine samples were evaluated to access the real sample application of the LLSME method by coupling with high-performance liquid chromatography (HPLC). Low limits of detection (0.006-0.02 microg L(-1)), satisfactory recoveries and good repeatability for real sample (RSD 1.2-9.6%, n = 5) were obtained. The method was demonstrated to be a fast, selective and sensitive pretreatment method for trace analysis of triazines

  16. Audit of the radioactive liquid waste treatment facility operations at the Los Alamos National Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-11-19

    Los Alamos National Laboratory (Los Alamos) generates radioactive and liquid wastes that must be treated before being discharged to the environment. Presently, the liquid wastes are treated in the Radioactive Liquid Waste Treatment Facility (Treatment Facility), which is over 30 years old and in need of repair or replacement. However, there are various ways to satisfy the treatment need. The objective of the audit was to determine whether Los Alamos cost effectively managed its Treatment Facility operations. The audit determined that Los Alamos` treatment costs were significantly higher when compared to similar costs incurred by the private sector. This situation occurred because Los Alamos did not perform a complete analysis of privatization or prepare a {open_quotes}make-or-buy{close_quotes} plan for its treatment operations, although a {open_quotes}make-or-buy{close_quotes} plan requirement was incorporated into the contract in 1996. As a result, Los Alamos may be spending $2.15 million more than necessary each year and could needlessly spend $10.75 million over the next five years to treat its radioactive liquid waste. In addition, Los Alamos has proposed to spend $13 million for a new treatment facility that may not be needed if privatization proves to be a cost effective alternative. We recommended that the Manager, Albuquerque Operations Office (Albuquerque), (1) require Los Alamos to prepare a {open_quotes}make-or-buy{close_quotes} plan for its radioactive liquid waste treatment operations, (2) review the plan for approval, and (3) direct Los Alamos to select the most cost effective method of operations while also considering other factors such as mission support, reliability, and long-term program needs. Albuquerque concurred with the recommendations.

  17. Amphiphilic antioxidants from "cashew nut shell liquid" (CNSL) waste.

    Science.gov (United States)

    Amorati, Riccardo; Attanasi, Orazio A; Favi, Gianfranco; Menichetti, Stefano; Pedulli, Gian Franco; Viglianisi, Caterina

    2011-03-07

    Hydrogenated cardanol and cardols, contained in industrial grade cardanol oil and obtained by distillation of the raw "cashew nut shell liquid" (CNSL), are easily transformed into efficient 4-thiaflavane antioxidants bearing a long alkyl chain on A ring and a catechol group on B ring.

  18. Production of Hydrocarbon Liquid by Thermal Pyrolysis of Paper Cup Waste

    Directory of Open Access Journals (Sweden)

    Bijayani Biswal

    2013-01-01

    Full Text Available The paper cup waste was pyrolysed in a stainless steel semibatch reactor at a temperature range of 325°C to 425°C and at a heating rate of 20°C min−1 with an aim to study the physical and chemical characteristics of the obtained hydrocarbon liquid and to determine its feasibility as a commercial fuel. The maximum liquid yield was 52% at 400°C. The functional groups present in the liquid are aldehydes, ketones, carboxylic acids, esters, alkenes, and alkanes. It was found that the pyrolytic liquid contains around 18 types of compounds having carbon chain length in the range of C6–C20. The obtained liquid can be used as valuable chemicals feedstock.

  19. Ionic Liquids for Utilization of Waste Heat from Distributed Power Generation Systems

    Energy Technology Data Exchange (ETDEWEB)

    Joan F. Brennecke; Mihir Sen; Edward J. Maginn; Samuel Paolucci; Mark A. Stadtherr; Peter T. Disser; Mike Zdyb

    2009-01-11

    The objective of this research project was the development of ionic liquids to capture and utilize waste heat from distributed power generation systems. Ionic Liquids (ILs) are organic salts that are liquid at room temperature and they have the potential to make fundamental and far-reaching changes in the way we use energy. In particular, the focus of this project was fundamental research on the potential use of IL/CO2 mixtures in absorption-refrigeration systems. Such systems can provide cooling by utilizing waste heat from various sources, including distributed power generation. The basic objectives of the research were to design and synthesize ILs appropriate for the task, to measure and model thermophysical properties and phase behavior of ILs and IL/CO2 mixtures, and to model the performance of IL/CO2 absorption-refrigeration systems.

  20. Capacity enhancement of aqueous borohydride fuels for hydrogen storage in liquids

    Energy Technology Data Exchange (ETDEWEB)

    Schubert, David; Neiner, Doinita [U.S. Borax Inc., Rio Tinto, Greenwood Village, CO (United States); Bowden, Mark [Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA (United States); Whittemore, Sean; Holladay, Jamie [Pacific Northwest National Laboratory, Richland, WA (United States); Huang, Zhenguo [Institute for Superconducting and Electronic Materials, University of Wollongong, Wollongong, NSW 2500 (Australia); Autrey, Tom [Pacific Northwest National Laboratory, Richland, WA (United States)

    2015-10-05

    Highlights: • Adjusting ratio of Q = Na/B will maximize H{sub 2} storage capacity of liquid carrier. • Mixtures of hydrolysis products are desirable to maximize solubility. • 6.5 wt.% hydrogen and remains liquid from beginning to end. - Abstract: In this work we demonstrate enhanced hydrogen storage capacities through increased solubility of sodium borate product species in aqueous media achieved by adjusting the sodium (NaOH) to boron (B(OH){sub 3}) ratio, i.e., M/B, to obtain a distribution of polyborate anions. For a 1:1 mol ratio of NaOH to B(OH){sub 3}, M/B = 1, the ratio of the hydrolysis product formed from NaBH{sub 4} hydrolysis, the sole borate species formed and observed by {sup 11}B NMR is sodium metaborate, NaB(OH){sub 4}. When the ratio is 1:3 NaOH to B(OH){sub 3}, M/B = 0.33, a mixture of borate anions is formed and observed as a broad peak in the {sup 11}B NMR spectrum. The complex polyborate mixture yields a metastable solution that is difficult to crystallize. Given the enhanced solubility of the polyborate mixture formed when M/B = 0.33 it should follow that the hydrolysis of sodium octahydrotriborate, NaB{sub 3}H{sub 8}, can provide a greater storage capacity of hydrogen for fuel cell applications compared to sodium borohydride while maintaining a single phase. Accordingly, the hydrolysis of a 23 wt.% NaB{sub 3}H{sub 8} solution in water yields a solution having the same complex polyborate mixture as formed by mixing a 1:3 M ratio of NaOH and B(OH){sub 3} and releases >8 eq of H{sub 2}. By optimizing the M/B ratio a complex mixture of soluble products, including B{sub 3}O{sub 3}(OH){sub 5}{sup 2−}, B{sub 4}O{sub 5}(OH){sub 4}{sup 2−}, B{sub 3}O{sub 3}(OH){sub 4}{sup −}, B{sub 5}O{sub 6}(OH){sub 4}{sup −} and B(OH){sub 3}, can be maintained as a single liquid phase throughout the hydrogen release process. Consequently, hydrolysis of NaB{sub 3}H{sub 8} can provide a 40% increase in H{sub 2} storage density compared to the hydrolysis

  1. Standard practice for analysis of aqueous leachates from nuclear waste materials using inductively coupled plasma-atomic emission spectrometry

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2010-01-01

    1.1 This practice is applicable to the determination of low concentration and trace elements in aqueous leachate solutions produced by the leaching of nuclear waste materials, using inductively coupled plasma-atomic emission spectroscopy (ICP-AES). 1.2 The nuclear waste material may be a simulated (non-radioactive) solid waste form or an actual solid radioactive waste material. 1.3 The leachate may be deionized water or any natural or simulated leachate solution containing less than 1 % total dissolved solids. 1.4 This practice should be used by analysts experienced in the use of ICP-AES, the interpretation of spectral and non-spectral interferences, and procedures for their correction. 1.5 No detailed operating instructions are provided because of differences among various makes and models of suitable ICP-AES instruments. Instead, the analyst shall follow the instructions provided by the manufacturer of the particular instrument. This test method does not address comparative accuracy of different devices...

  2. A review on applicability of naturally available adsorbents for the removal of hazardous dyes from aqueous waste.

    Science.gov (United States)

    Sharma, Pankaj; Kaur, Harleen; Sharma, Monika; Sahore, Vishal

    2011-12-01

    The effluent water of many industries, such as textiles, leather, paper, printing, cosmetics, etc., contains large amount of hazardous dyes. There is huge number of treatment processes as well as adsorbent which are available for the processing of this effluent water-containing dye content. The applicability of naturally available low cast and eco-friendly adsorbents, for the removal of hazardous dyes from aqueous waste by adsorption treatment, has been reviewed. In this review paper, we have provided a compiled list of low-cost, easily available, safe to handle, and easy-to-dispose-off adsorbents. These adsorbents have been classified into five different categories on the basis of their state of availability: (1) waste materials from agriculture and industry, (2) fruit waste, (3) plant waste, (4) natural inorganic materials, and (5) bioadsorbents. Some of the treated adsorbents have shown good adsorption capacities for methylene blue, congo red, crystal violet, rhodamine B, basic red, etc., but this adsorption process is highly pH dependent, and the pH of the medium plays an important role in the treatment process. Thus, in this review paper, we have made some efforts to discuss the role of pH in the treatment of wastewater.

  3. Utilization of municipal solid and liquid wastes for bioenergy and bioproducts production.

    Science.gov (United States)

    Chen, Paul; Xie, Qinglong; Addy, Min; Zhou, Wenguang; Liu, Yuhuan; Wang, Yunpu; Cheng, Yanling; Li, Kun; Ruan, Roger

    2016-09-01

    Municipal wastes, be it solid or liquid, are rising due to the global population growth and rapid urbanization and industrialization. Conventional management practice involving recycling, combustion, and treatment/disposal is deemed unsustainable. Solutions must be sought to not only increase the capacity but also improve the sustainability of waste management. Research has demonstrated that the non-recyclable waste materials and bio-solids can be converted into useable heat, electricity, or fuel and chemical through a variety of processes, including gasification, pyrolysis, anaerobic digestion, and landfill gas in addition to combustion, and wastewater streams have the potential to support algae growth and provide other energy recovery options. The present review is intended to assess and analyze the current state of knowledge in the municipal solid wastes and wastewater treatment and utilization technologies and recommend practical solution options and future research and development needs.

  4. Relative hydrophobicity between the phases and partition of cytochrome-c in glycine ionic liquids aqueous two-phase systems.

    Science.gov (United States)

    Wu, Changzeng; Wang, Jianji; Li, Zhiyong; Jing, Jun; Wang, Huiyong

    2013-08-30

    In this work, glycine ionic liquids tetramethylammonium glycine ([N1111][Gly]), tetraethylammonium glycine ([N2222][Gly]), tetra-n-butylammonium glycine ([N4444][Gly]), tetra-n-butylphosphonium glycine ([P4444][Gly]) and tetra-n-pentylammonium glycine ([N5555][Gly]) were synthesized and used to prepare aqueous two-phase systems (ATPSs) in the presence of K2HPO4. Binodal curves of such ATPSs and partition coefficients of a series of dinitrophenylated (DNP) amino acids in these ATPSs were determined at 298.15K to understand the effect of cationic structure of the ionic liquids on the phase-forming ability of glycine ionic liquids, relative hydrophobicity between the phases in the ionic liquids ATPSs, and polarity of the ionic liquids-rich phases. With the attempt to correlate the relative hydrophobicity of the phases in the ATPSs with their extraction capability for proteins, partition coefficients of cytochrome-c in the ATPSs were also determined. It was shown that partition coefficients of cytochrome-c were in the range from 2.83 to 20.7 under the studied pH conditions. Then, hydrophobic interactions between cytochrome-c and the ionic liquid are suggested to be the main driving force for the preferential partition of cytochrome-c in the glycine ionic liquid-rich phases of the ATPSs. Result derived from polarity of the ionic liquids-rich phases supports this mechanism.

  5. Momentum, heat, and neutral mass transport in convective atmospheric pressure plasma-liquid systems and implications for aqueous targets

    Science.gov (United States)

    Lindsay, Alexander; Anderson, Carly; Slikboer, Elmar; Shannon, Steven; Graves, David

    2015-10-01

    There is a growing interest in the study of plasma-liquid interactions with application to biomedicine, chemical disinfection, agriculture, and other fields. This work models the momentum, heat, and neutral species mass transfer between gas and aqueous phases in the context of a streamer discharge; the qualitative conclusions are generally applicable to plasma-liquid systems. The problem domain is discretized using the finite element method. The most interesting and relevant model result for application purposes is the steep gradients in reactive species at the interface. At the center of where the reactive gas stream impinges on the water surface, the aqueous concentrations of OH and ONOOH decrease by roughly 9 and 4 orders of magnitude respectively within 50 μ m of the interface. Recognizing the limited penetration of reactive plasma species into the aqueous phase is critical to discussions about the therapeutic mechanisms for direct plasma treatment of biological solutions. Other interesting results from this study include the presence of a 10 K temperature drop in the gas boundary layer adjacent to the interface that arises from convective cooling. Though the temperature magnitudes may vary among atmospheric discharge types (different amounts of plasma-gas heating), this relative difference between gas and liquid bulk temperatures is expected to be present for any system in which convection is significant. Accounting for the resulting difference between gas and liquid bulk temperatures has a significant impact on reaction kinetics; factor of two changes in terminal aqueous species concentrations like H2O2, NO2- , and NO3- are observed in this study if the effect of evaporative cooling is not included.

  6. Tailoring the interfaces between nematic liquid crystal emulsions and aqueous phases via layer-by-layer assembly.

    Science.gov (United States)

    Tjipto, Elvira; Cadwell, Katie D; Quinn, John F; Johnston, Angus P R; Abbott, Nicholas L; Caruso, Frank

    2006-10-01

    We report the assembly of polyelectrolyte multilayer (PEM) films at the interfaces of thermotropic liquid crystal (LC) droplets dispersed in an aqueous phase. Exposure of PEM-coated droplets to surfactant slowed the bipolar-to-radial ordering transition of the LCs by 2 orders of magnitude relative to naked droplets. This shows that PEMs can be used to influence the interactions of analytes with the LC cores of the droplets, allowing tuning of the LC emulsion sensing properties.

  7. The Utilization of Banana Peel in the Fermentation Liquid in Food Waste Composting

    Science.gov (United States)

    Kadir, A. A.; Rahman, N. A.; Azhari, N. W.

    2016-07-01

    Municipal solid waste in Malaysia contains a high amount of organic matters, particularly food waste. Food waste represents almost 60% from the total municipal solid waste disposed in the landfill. Food waste can be converted into useful materials such as compost. However, source separation of food waste for recycling is not commonly practiced in Malaysia due to various constraints. These constraints include low awareness among the waste generators and low demand of the products produced from the food waste such as composts. Composting is one of the alternatives that can be used in food waste disposal from Makanan Ringan Mas. The aim of the study is to convert food waste generated from Makanan Ringan Mas which is a medium sale industry located at Parit Kuari Darat, Batu Pahat by using composting method. The parameters which include temperature, pH value, NPK (Nitrogen, Phosphorus, Potassium) values has been examined. Banana peel is being used as the fermentation liquid whilst soil and coconut husk were used as the composting medium. Based on the results during the composting process, most of the pH value in each reactor is above 5 and approximately at neutral. This shown that the microbial respiration in the well controlled composting reactor was inhibited and had approached the mature phase. On the other hand, during the period of composting, the overall temperature range from 25 °C to 47 °C which shown the active phase for composting will occoured. As for NPK content Nitrogen value range is 35325 mg/L to 78775 mg/L, Phosphorus, 195.83 mg/L to 471 mg/L and potassium is 422.3 mg/L to 2046 mg/L which is sufficient to use for agricultural purpose. The comparison was made with available organic compost in the market and only showed slightly difference. Nevertheless, in comparison with common fertilizer, the NPK value of organic compost are considerably very low.

  8. Leaching and recycling of zinc from liquid waste sediments

    Institute of Scientific and Technical Information of China (English)

    PENG Bing; GAO Hui-mei; CHAI Li-yuan; SHU Yu-de

    2008-01-01

    The selective leaching and recovery of zinc in a zinciferous sediment from a synthetic wastewater treatment was investigated. The main composition of the sediment includes 6% zinc and other metal elements such as Ca, Fe, Cu, Mg. The effects of sulfuric acid concentration, temperature, leaching time and the liquid-to-solid ratio on the leaching rate of zinc were studied by single factor and orthogonal experiments. The maximum difference of leaching rate between zinc and iron, 89.85%, was obtained by leaching under 170 g/L H2SO4 in liquid-to-solid ratio 4.2 mL/g at 65 "C for 1 h, and the leaching rates of zinc and iron were 91.20% and 1.35%, respectively.

  9. Removal of non aqueous phase liquid liquid (NAPL) from a loam soil monitored by time domain reflectometry (TDR) technique

    Science.gov (United States)

    comegna, alessandro; coppola, Antonio; dragonetti, giovanna; ajeel, ali; saeed, ali; sommella, angelo

    2016-04-01

    Non-aqueous phase liquids (NAPLs) are compounds with low or no solubility with water. These compounds, due to the several human activities, can be accidentally introduced in the soil system and thus constitute a serious geo-environmental problem, given the toxicity level and the high mobility. The remediation of contaminated soil sites requires knowledge of the contaminant distribution in the soil profile and groundwater. Methods commonly used to characterize contaminated sites are coring, soil sampling and the installation of monitoring wells for the collection of groundwater samples. The main objective of the present research is to explore the potential application of time domain reflectometry (TDR) technique in order to evaluate the effect of contaminant removal in a loam soil, initially contaminated with NAPL and then flushed with different washing solutions. The experimental setup consist of: i) a Techtronix cable tester; ii) a three-wire TDR probe with wave guides 14.5 cm long inserted vertically into the soil samples; iii) a testing cell of 8 cm in diameter and 15 cm high; iv) a peristaltic pump for upward injection of washing solution. In laboratory, soil samples were oven dried at 105°C and passed through a 2 mm sieve. Known quantities of soil and NAPL (corn oil, a non-volatile and non-toxic organic compound) were mixed in order to obtain soil samples with different degrees of contamination. Once a soil sample was prepared, it was repacked into a plastic cylinder and then placed into the testing cell. An upward injection of washing solution was supplied to the contaminated sample with a rate q=1.5 cm3/min, which corresponds to a darcian velocity v=6.0 cm/h. The out coming fluid, from the soil column was collected, then the washing solution and oil was separated. Finally both the amount of oil that was remediated and the dielectric permittivity (measured via TDR) of the contaminated soil sample were recorded. Data collected were employed to implement a

  10. Equilibrium, kinetic and thermodynamic studies for sorption of Ni (II from aqueous solution using formaldehyde treated waste tea leaves

    Directory of Open Access Journals (Sweden)

    Jasmin Shah

    2015-05-01

    Full Text Available The sorption characteristic of Ni (II from aqueous solution using formaldehyde treated waste tea leaves as a low cost sorbent has been studied. The effect of pH, contact time, sorbent dose, initial metal ion concentration and temperature were investigated in batch experiments. The equilibrium data were fitted into four most common isotherm models; Freundlich, Langmuir, Tempkin and Dubinin–Radushkevich (D–R. The Langmuir model described the sorption isotherm best with maximum monolayer sorption capacity of 120.50 mg g−1. Four kinetic models, pseudo-first-order, pseudo-second-order, intraparticle diffusion and Elovich were employed to explain the sorption mechanism. The kinetics of sorption data showed that the pseudo-second-order model is the best with correlation coefficient of 0.9946. The spontaneous and exothermic nature of the sorption process was revealed from thermodynamic investigations. The effect of some common alkali and alkaline earth metal ions were also studied which showed that the presence of these ions have no effect on the sorption of Ni (II. The results showed that waste tea leaves have the potential to be used as a low cost sorbent for the removal of Ni (II from aqueous solutions.

  11. Oak Ridge National Lebroatory Liquid&Gaseous Waste Treatment System Strategic Plan

    Energy Technology Data Exchange (ETDEWEB)

    Van Hoesen, S.D.

    2003-09-09

    Excellence in Laboratory operations is one of the three key goals of the Oak Ridge National Laboratory (ORNL) Agenda. That goal will be met through comprehensive upgrades of facilities and operational approaches over the next few years. Many of ORNL's physical facilities, including the liquid and gaseous waste collection and treatment systems, are quite old, and are reaching the end of their safe operating life. The condition of research facilities and supporting infrastructure, including the waste handling facilities, is a key environmental, safety and health (ES&H) concern. The existing infrastructure will add considerably to the overhead costs of research due to increased maintenance and operating costs as these facilities continue to age. The Liquid Gaseous Waste Treatment System (LGWTS) Reengineering Project is a UT-Battelle, LLC (UT-B) Operations Improvement Program (OIP) project that was undertaken to develop a plan for upgrading the ORNL liquid and gaseous waste systems to support ORNL's research mission.

  12. Tandem Extraction/Liquid Chromatography-Mass Spectrometry Protocol for the Analysis of Acrylamide and Surfactant-related Compounds in Complex Aqueous Environmental Samples

    Science.gov (United States)

    The development of a liquid chromatography‐mass spectrometry (LC‐MS)‐based strategy for the detection and quantitation of acrylamide and surfactant‐related compounds in aqueous complex environmental samples.

  13. Self-assembly and antimicrobial activity of long-chain amide-functionalized ionic liquids in aqueous solution.

    Science.gov (United States)

    Garcia, M Teresa; Ribosa, Isabel; Perez, Lourdes; Manresa, Angeles; Comelles, Francesc

    2014-11-01

    Surface active amide-functionalized ionic liquids (ILs) consisting of a long alkyl chain (C6C14) connected to a polar head group (methylimidazolium or pyridinium cation) via an amide functional group were synthesized and their thermal stability, micellar properties and antimicrobial activity in aqueous solution investigated. The incorporation of an amide group increased the thermal stability of the functionalized ionic liquids compared to simple alkyl chain substituted ionic liquids. The surface activity and aggregation behaviour in aqueous solution of amide-functionalized ionic liquids were examined by tensiometry, conductivity and spectrofluorimetry. Amide-functionalized ILs displayed surface activity and their critical micelle concentration (cmc) in aqueous media decreased with the elongation of the alkyl side chain as occurs for typical surfactants. Compared to non-functionalized ILs bearing the same alkyl chain, ionic liquids with an amide moiety possess higher surface activity (pC20) and lower cmc values. The introduction of an amide group in the hydrophobic chain close to the polar head enhances adsorption at the air/water interface and micellization which could be attributed to the H-bonding in the headgroup region. The antimicrobial activity was evaluated against a panel of representative Gram-negative and Gram-positive bacteria and fungi. Amide-functionalized ILs with more than eight carbon atoms in the side chain showed broad antimicrobial activity. Antibacterial activities were found to increase with the alkyl chain length being the C12 homologous the most effective antimicrobial agents. The introduction of an amide group enhanced significantly the antifungal activity as compared to non-functionalized ILs.

  14. Treatability study of absorbent polymer waste form for mixed waste treatment

    Energy Technology Data Exchange (ETDEWEB)

    Herrmann, S. D.; Lehto, M. A.; Stewart, N. A.; Croft, A. D.; Kern, P. W.

    2000-02-10

    A treatability study was performed to develop and characterize an absorbent polymer waste form for application to low level (LLW) and mixed low level (MLLW) aqueous wastes at Argonne National Laboratory-West (ANL-W). In this study absorbent polymers proved effective at immobilizing aqueous liquid wastes in order to meet Land Disposal Restrictions for subsurface waste disposal. Treatment of aqueous waste with absorbent polymers provides an alternative to liquid waste solidification via high-shear mixing with clays and cements. Significant advantages of absorbent polymer use over clays and cements include ease of operations and waste volume minimization. Absorbent polymers do not require high-shear mixing as do clays and cements. Granulated absorbent polymer is poured into aqueous solutions and forms a gel which passes the paint filter test as a non-liquid. Pouring versus mixing of a solidification agent not only eliminates the need for a mixing station, but also lessens exposure to personnel and the potential for spread of contamination from treatment of radioactive wastes. Waste minimization is achieved as significantly less mass addition and volume increase is required of and results from absorbent polymer use than that of clays and cements. Operational ease and waste minimization translate into overall cost savings for LLW and MLLW treatment.

  15. Characterization of radioactive organic liquid wastes; Caracterizacion de desechos liquidos organicos radiactivos

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez A, I.; Monroy G, F.; Quintero P, E.; Lopez A, E.; Duarte A, C., E-mail: ivonne-arce@hotmail.com [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2014-10-15

    With the purpose of defining the treatment and more appropriate conditioning of radioactive organic liquid wastes, generated in medical establishments and research centers of the country (Mexico) and stored in drums of 208 L is necessary to characterize them. This work presents the physical-chemistry and radiological characterization of these wastes. The samples of 36 drums are presented, whose registrations report the presence of H-3, C-14 and S-35. The following physiochemical parameters of each sample were evaluated: ph, conductivity, density and viscosity; and analyzed by means of gamma spectrometry and liquid scintillation, in order to determine those contained radionuclides in the same wastes and their activities. Our results show the presence of H-3 (61%), C-14 (13%) and Na-22 (11%) and in some drums low concentrations of Co-60 (5.5%). In the case of the registered drums with S-35 (8.3%) does not exist presence of radioactive material, so they can be liberated without restriction as conventional chemical wastes. The present activities in these wastes vary among 5.6 and 2312.6 B g/g, their ph between 2 and 13, the conductivities between 0.005 and 15 m S, the densities among 1.05 and 1.14, and the viscosities between 1.1 and 39 MPa. (Author)

  16. Design of functional guanidinium ionic liquid aqueous two-phase systems for the efficient purification of protein

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Xueqin; Wang, Yuzhi, E-mail: wyzss@hnu.edu.cn; Zeng, Qun; Chen, Jing; Huang, Yanhua; Xu, Kaijia

    2014-03-01

    Graphical abstract: - Highlights: • A series of novel cationic functional hexaalkylguanidinium ionic liquids and anionic functional tetraalkylguanidinium ionic liquids have been synthesized. • Functional guanidinium ionic liquid aqueous two-phase systems have been first designed for the purification of protein. • Mechanisms and performances of the process were researched. • Simple, green, safety and presents better purified ability than ordinary process. • A potential efficient platform for protein purification and related studies. - Abstract: A series of novel cationic functional hexaalkylguanidinium ionic liquids and anionic functional tetraalkylguanidinium ionic liquids have been devised and synthesized based on 1,1,3,3-tetramethylguanidine. The structures of the ionic liquids (ILs) were confirmed by {sup 1}H nuclear magnetic resonance ({sup 1}H NMR) and 13C nuclear magnetic resonance (13C NMR) and the production yields were all above 90%. Functional guanidinium ionic liquid aqueous two-phase systems (FGIL-ATPSs) have been first designed with these functional guanidinium ILs and phosphate solution for the purification of protein. After phase separation, proteins had transferred into the IL-rich phase and the concentrations of proteins were determined by measuring the absorbance at 278 nm using an ultra violet visible (UV–vis) spectrophotometer. The advantages of FGIL-ATPSs were compared with ordinary ionic liquid aqueous two-phase systems (IL-ATPSs). The proposed FGIL-ATPS has been applied to purify lysozyme, trypsin, ovalbumin and bovine serum albumin. Single factor experiments were used to research the effects of the process, such as the amount of ionic liquid (IL), the concentration of salt solution, temperature and the amount of protein. The purification efficiency reaches to 97.05%. The secondary structure of protein during the experimental process was observed upon investigation using UV–vis spectrophotometer, Fourier-transform infrared

  17. Techniques and Facilities for Handling and Packaging Tritiated Liquid Wastes for Burial

    Energy Technology Data Exchange (ETDEWEB)

    Rhinehammer, T. B.; Mershad, E. A.

    1974-06-01

    Methods and facilities have been developed for the collection, storage, measurement, assay, solidification, and packaging of tritiated liquid wastes (concentrations up to 5 Ci/ml) for disposal by land burial. Tritium losses to the environment from these operations are less than 1 ppm. All operations are performed in an inert gas-purged glovebox system vented to an effluent removal system which permits nearly complete removal of tritium from the exhaust gases prior to their dischardge to the environment. Waste oil and water from tritium processing areas are vacuum-transferred to glovebox storage tanks through double-walled lines. Accommodations are also available for emptying portable liquid waste containers and for removing tritiated water from molecular sieve beds with heat and vacuum. The tritium concentration of the collected liquids is measured by an in-line calorimeter. A low-volume metering pump is used to transfer liquids from holding tanks to heavy walled polyethylene drums filled with an absorbent or cement for solidification. Final packaging of the sealed polyethylene drums is in either an asphalt-filled combination 30- and 55- gallon metal drum package or a 30-gallon welded stainless steel container.

  18. Modeling and measurements of solid-liquid and vapor-liquid equilibria of polyols and carbohydrates in aqueous solution

    DEFF Research Database (Denmark)

    Jonsdottir, Svava Osk; Cooke, S.A.; Macedo, E.A.

    2002-01-01

    calculated with molecular mechanics methods has shown to give good predictions of the phase behavior of a variety of mixtures, including glycols and small saccharides in aqueous solution. The method is completely predictive, as the strength of the molecular interactions is determined with a theoretical...... and saccharides in aqueous solution have been predicted with this method, giving results in excellent agreement with the experimental values....

  19. High-temperature vitrification of Hanford residual-liquid waste in a continuous melter

    Energy Technology Data Exchange (ETDEWEB)

    Barnes, S.M.

    1980-04-01

    Over 270 kg of high-temperature borosilicate glass have been produced in a series of three short-term tests in the High-Temperature Ceramic Melter vitrification system at PNL. The glass produced was formulated to vitrify simulated Hanford residual-liquid waste. The tests were designed to (1) demonstrate the feasibility of utilizing high-temperature, continuous-vitrification technology for the immobilization of the residual-liquid waste, (2) test the airlift draining technique utilized by the high-temperature melter, (3) compare glass produced in this process to residual-liquid glass produced under laboratory conditions, (4) investigate cesium volatility from the melter during waste processing, and (5) determine the maximum residual-liquid glass production rate in the high-temperature melter. The three tests with the residual-liquid composition confirmed the viability of the continuous-melting vitrification technique for the immobilization of this waste. The airlift draining technique was demonstrated in these tests and the glass produced from the melter was shown to be less porous than the laboratory-produced glass. The final glass produced from the second test was compared to a glass of the same composition produced under laboratory conditions. The comparative tests found the glasses to be indistinguishable, as the small differences in the test results fell within the precision range of the characterization testing equipment. The cesium volatility was examined in the final test. This examination showed that 0.44 wt % of the cesium (assumed to be cesium oxide) was volatilized, which translates to a volatilization rate of 115 mg/cm/sup 2/-h.

  20. Treatment of Zn-Containing Acidic Waste Water by Emulsion Liquid Membrane Process

    Institute of Scientific and Technical Information of China (English)

    王士柱; 何培炯; 郝东萍; 朱永贝睿

    2002-01-01

    Zn-containing waste water from a viscose staple fiber plant has been treated using the emulsion liquid membrane (ELM) process since 1995. The flow sheet and operating parameters of the ELM process are introduced. After adjusting the membrane composition, changing the emulsion phase ratio, and adding a scrubbing step, the ELM process operated normally without trouble for emulsion splitting and mass transport throughput. The splitter voltage was decreased to 3.55 kV. The zinc concentration of treated waste water was lowered to less than 10 mgL-1. More than 95% of the zinc was recovered and reused.

  1. Electrochemical, computational and spectroscopic investigation on local environment of plutonium in ionic liquid and aqueous medium. A comparative study

    Energy Technology Data Exchange (ETDEWEB)

    Sengupta, Arijit; Murali, Mallekav S.; Mohapatra, Prasanta Kumar [Bhabha Atomic Research Centre Trombay, Mumbai (India). Radiochemistry Div.; Ali, Sk. Musharaf; Shenoy, Kalsanka Trivikram [Bhabha Atomic Research Centre Trombay, Mumbai (India). Chemical Engineering Div.

    2016-07-01

    With an aim to understand the nature of species, cyclic voltammetry (CV) of Pu(IV) in dilute HBr and in a room temperature ionic liquid (RTIL), 1-octyl-3-methylimidazolium bromide (C{sub 8}mimBr) was carried out. Shifts of cathodic and anodic peak potentials of Pu(IV) cyclic voltammograms were observed towards negative potentials in the extended electrochemical window for ionic liquid medium compared to 2 M HBr. The diffusion coefficient of the most likely species of Pu(IV) in aqueous medium was found to be greater than that of the corresponding species in ionic liquid while the activation energy showed reverse trend. The Pu(IV)/Pu(III) redox reaction was found to be exothermic in aqueous medium while it was endothermic in C{sub 8}mimBr. The redox reaction was found to be quasi reversible for both the media while the extent of irreversibility was more in ionic liquid. UV-Vis spectroscopy of Pu in these media showed significant differences in the peak positions and their relative intensities, indicating the possible differences in the interactions of Pu(IV) with the solvent molecules resulting in speciation differences. A new prominent peak was observed in RTIL which could be for a new species of Pu(IV). Computational studies were also carried out to understand the solvation of Pu and the possibility of thermodynamic conversion from Pu(IV) to Pu(III).

  2. Direct extraction of genomic DNA from maize with aqueous ionic liquid buffer systems for applications in genetically modified organisms analysis.

    Science.gov (United States)

    Gonzalez García, Eric; Ressmann, Anna K; Gaertner, Peter; Zirbs, Ronald; Mach, Robert L; Krska, Rudolf; Bica, Katharina; Brunner, Kurt

    2014-12-01

    To date, the extraction of genomic DNA is considered a bottleneck in the process of genetically modified organisms (GMOs) detection. Conventional DNA isolation methods are associated with long extraction times and multiple pipetting and centrifugation steps, which makes the entire procedure not only tedious and complicated but also prone to sample cross-contamination. In recent times, ionic liquids have emerged as innovative solvents for biomass processing, due to their outstanding properties for dissolution of biomass and biopolymers. In this study, a novel, easily applicable, and time-efficient method for the direct extraction of genomic DNA from biomass based on aqueous-ionic liquid solutions was developed. The straightforward protocol relies on extraction of maize in a 10 % solution of ionic liquids in aqueous phosphate buffer for 5 min at room temperature, followed by a denaturation step at 95 °C for 10 min and a simple filtration to remove residual biopolymers. A set of 22 ionic liquids was tested in a buffer system and 1-ethyl-3-methylimidazolium dimethylphosphate, as well as the environmentally benign choline formate, were identified as ideal candidates. With this strategy, the quality of the genomic DNA extracted was significantly improved and the extraction protocol was notably simplified compared with a well-established method.

  3. Drop Dynamics and Speciation in Isolation of Metals from Liquid Wastes by Reactive Scavenging

    Energy Technology Data Exchange (ETDEWEB)

    Arne J. Pearlstein; Alexander Scheeline

    2002-08-30

    Computational and experimental studies of the motion and dynamics of liquid drops in gas flows were conducted with relevance to reactive scavenging of metals from atomized liquid waste. Navier-Stoke's computations of deformable drops revealed a range of conditions from which prolate drops are expected, and showed how frajectiones of deformable drops undergoing deceleration can be computed. Experimental work focused on development of emission fluorescence, and scattering diagnostics. The instrument developed was used to image drop shapes, soot, and nonaxisymmetric departures from steady flow in a 22kw combustor

  4. Application of dispersive Liquid-Liquid microextraction based on solidification of floating organic droplet multi-residue method for the simultaneous determination of polychlorinated biphenyls, organochlorine, and pyrethroid pesticides in aqueous sample

    Energy Technology Data Exchange (ETDEWEB)

    Zuo, Mei; Li, Man-Liang [Enshi Prefecture Tobacco Company, Enshi, Hubei (China); Cheng, Jing; Matsadiq, Guzalnur; Liu, Lu; Zhang, Miao [Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan (China)

    2012-12-15

    Dispersive liquid-liquid microextraction based on solidification of floating organic droplet (DLLME-SFO) technique was successfully applied for simultaneous assay of eight polychlorinated biphenyls, two organochlorine, and four pyrethroid pesticides multi-residue in aqueous samples by using GC-electron capture detection. The effects of various parameters such as kind of extractant and dispersant and volume of them, extraction time, effect of salt addition, and pH were optimized. As a result, 5.0 {mu}L 1-dodecanol was chosen as extraction solvent, 600 {mu}L methanol were used as dispersive solvent without salt addition, pH was adjusted to 7. Under the optimized conditions, the limits of detection (LOD) were ranged from 1.4 to 8.3 ng L{sup -1}. Satisfactory linear range was observed from 5.0 to 2000 ng L{sup -1} with correlation coefficient better than 0.9909. Good precisions were also acquired with RSD better than 13.6% for all target analytes. The enrichment factors of the method were ranged from 786 to 1427. The method can be successfully applied to simultaneous separation and determination of three class residues in real water samples and good recoveries were obtained ranging from 76 to 130, 73 to 129, and 78 to 130% for tap water, lake water, and industrial waste water, respectively. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  5. Design of functional guanidinium ionic liquid aqueous two-phase systems for the efficient purification of protein.

    Science.gov (United States)

    Ding, Xueqin; Wang, Yuzhi; Zeng, Qun; Chen, Jing; Huang, Yanhua; Xu, Kaijia

    2014-03-07

    A series of novel cationic functional hexaalkylguanidinium ionic liquids and anionic functional tetraalkylguanidinium ionic liquids have been devised and synthesized based on 1,1,3,3-tetramethylguanidine. The structures of the ionic liquids (ILs) were confirmed by (1)H nuclear magnetic resonance ((1)H NMR) and 13C nuclear magnetic resonance (13C NMR) and the production yields were all above 90%. Functional guanidinium ionic liquid aqueous two-phase systems (FGIL-ATPSs) have been first designed with these functional guanidinium ILs and phosphate solution for the purification of protein. After phase separation, proteins had transferred into the IL-rich phase and the concentrations of proteins were determined by measuring the absorbance at 278 nm using an ultra violet visible (UV-vis) spectrophotometer. The advantages of FGIL-ATPSs were compared with ordinary ionic liquid aqueous two-phase systems (IL-ATPSs). The proposed FGIL-ATPS has been applied to purify lysozyme, trypsin, ovalbumin and bovine serum albumin. Single factor experiments were used to research the effects of the process, such as the amount of ionic liquid (IL), the concentration of salt solution, temperature and the amount of protein. The purification efficiency reaches to 97.05%. The secondary structure of protein during the experimental process was observed upon investigation using UV-vis spectrophotometer, Fourier-transform infrared spectroscopy (FT-IR) and circular dichroism spectrum (CD spectrum). The precision, stability and repeatability of the process were investigated. The mechanisms of purification were researched by dynamic light scattering (DLS), determination of the conductivity and transmission electron microscopy (TEM). It was suggested that aggregation and embrace phenomenon play a significant role in the purification of proteins. All the results show that FGIL-ATPSs have huge potential to offer new possibility in the purification of proteins.

  6. Capacity enhancement of aqueous borohydride fuels for hydrogen storage in liquids

    Energy Technology Data Exchange (ETDEWEB)

    Schubert, David [U.S. Borax Inc., Rio Tinto, CO (United States); Neiner, Doinita [U.S. Borax Inc., Rio Tinto, CO (United States); Bowden, Mark [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Whittemore, Sean [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Holladay, Jamie [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Huang, Zhenguo [Univ. of Wollongong, NSW (Australia); Autrey, Tom [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2015-10-01

    In this work we demonstrate enhanced hydrogen storage capacities through increased solubility of sodium borate product species in aqueous media achieved by adjusting the sodium (NaOH) to boron (B(OH)3) ratio, i.e., M/B, to obtain a distribution of polyborate anions. For a 1:1 mole ratio of NaOH to B(OH)3, M/B = 1, the ratio of the hydrolysis product formed from NaBH4 hydrolysis, the sole borate species formed and observed by 11B NMR is sodium metaborate, NaB(OH)4. When the ratio is 1:3 NaOH to B(OH)3, M/B = 0.33, a mixture of borate anions is formed and observed as a broad peak in the 11B NMR spectrum. The complex polyborate mixture yields a metastable solution that is difficult to crystallize. Given the enhanced solubility of the polyborate mixture formed when M/B = 0.33 it should follow that the hydrolysis of sodium octahydrotriborate, NaB3H8, can provide a greater storage capacity of hydrogen for fuel cell applications compared to sodium borohydride while maintaining a single phase. Accordingly, the hydrolysis of a 23 wt% NaB3H8 solution in water yields a solution having the same complex polyborate mixture as formed by mixing a 1:3 molar ratio of NaOH and B(OH)3 and releases >8 eq of H2. By optimizing the M/B ratio a complex mixture of soluble products, including B3O3(OH)52-, B4O5(OH)42-, B3O3(OH)4-, B5O6(OH)4- and B(OH)3, can be maintained as a single liquid phase throughout the hydrogen release process. Consequently, hydrolysis of NaB3H8 can provide a 40% increase in H2 storage density compared to the hydrolysis of NaBH4 given the decreased solubility of sodium metaborate. The authors would like to thank Jim Sisco and Paul Osenar of

  7. Effect of liquid-sheet thickness on detection sensitivity for laser-induced breakdown spectroscopy of aqueous solution.

    Science.gov (United States)

    Ohba, Hironori; Saeki, Morihisa; Wakaida, Ikuo; Tanabe, Rie; Ito, Yoshiro

    2014-10-01

    For aqueous-solution-based elemental analysis, we used a thin liquid sheet (μm-scale thickness) in laser-induced breakdown spectroscopy with nanosecond laser pulses. Laser-induced plasma is emitted by focusing a pulsed Nd:YAG laser (1064 nm) on a 5- to 80-μm-thick liquid sheet in air. To optimize the conditions for detecting elements, we studied how the signal-to-background ratio (SBR) for Hα Balmer and Na-neutral emission lines depends on the liquid-sheet thickness. The SBR of the Hα Balmer and Na-neutral lines was maximized for a sheet thickness of ~20 μm at the laser energy of 100 mJ. The hydrodynamics of liquid flow induced by the laser pulse was analyzed by laser flash shadowgraph imaging. Time-resolved observation of the hydrodynamics and plasma emission suggests that the dependence of the SBR on the liquid-sheet thickness is correlated with the volume of flowing liquid that interacts with the laser pulses.

  8. Isolation of Metals from Liquid Wastes: Reactive Scavenging in Turbulent Thermal Reactors

    Energy Technology Data Exchange (ETDEWEB)

    Jost O.L. Wendt; Alan R. Kerstein; Alexander Scheeline; Arne Pearlstein; William Linak

    2003-08-06

    The Overall project demonstrated that toxic metals (cesium Cs and strontium Sr) in aqueous and organic wastes can be isolated from the environment through reaction with kaolinite based sorbent substrates in high temperature reactor environments. In addition, a state-of-the art laser diagnostic tool to measure droplet characteristic in practical 'dirty' laboratory environments was developed, and was featured on the cover of a recent edition of the scientific journal ''applied Spectroscopy''. Furthermore, great strides have been made in developing a theoretical model that has the potential to allow prediction of the position and life history of every particle of waste in a high temperature, turbulent flow field, a very challenging problem involving as it does, the fundamentals of two phase turbulence and of particle drag physics.

  9. A resolution approach of racemic phenylalanine with aqueous two-phase systems of chiral tropine ionic liquids.

    Science.gov (United States)

    Wu, Haoran; Yao, Shun; Qian, Guofei; Yao, Tian; Song, Hang

    2015-10-30

    Aqueous two-phase systems (ATPS) based on tropine type chiral ionic liquids and inorganic salt solution were designed and prepared for the enantiomeric separation of racemic phenylalanine. The phase behavior of IL-based ATPS was comprehensive investigated, and phase equilibrium data were correlated by Merchuk equation. Various factors were also systematically investigated for their influence on separation efficiency. Under the appropriate conditions (0.13g/g [C8Tropine]pro, 35mg/g Cu(Ac)2, 20mg/g d,l-phenylalanine, 0.51g/g H2O and 0.30g/g K2HPO4), the enantiomeric excess value of phenylalanine in solid phase (mainly containing l-enantiomer) was 65%. Finally, the interaction mechanism was studied via 1D and 2D NMR. The results indicate that d-enantiomer of phenylalanine interacts more strongly with chiral ILs and Cu(2+) based on the chiral ion-pairs space coordination mechanism, which makes it tend to remain in the top IL-rich phase. By contrast, l-enantiomer is transferred into the solid phase. Above chiral ionic liquids aqueous two-phase systems have demonstrated obvious resolution to racemic phenylalanine and could be promising alterative resolution approach for racemic amino acids in aqueous circumstance.

  10. Determination of aromatic amines in aqueous extracts of polyurethane foam using hydrophilic interaction liquid chromatography and mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Riddar Johnson, Jakob, E-mail: jakob.riddarjohnson@anchem.su.se [Work Environment Chemistry, Stockholm University, P.O. Box 460, 281 24 Haessleholm (Sweden); Karlsson, Daniel; Dalene, Marianne; Skarping, Gunnar [Work Environment Chemistry, Stockholm University, P.O. Box 460, 281 24 Haessleholm (Sweden)

    2010-09-23

    A method is presented for the determination of aromatic amines in aqueous extracts of polyurethane (PUR) foam. The method is based on the extraction of PUR foam using aqueous acetic acid (0.1%, w/v) followed by determination of extracted aromatic amines using hydrophilic interaction liquid chromatography (HILIC) and tandem mass spectrometry (MS/MS) with positive electrospray ionisation. The injections of volumes up to 5 {mu}L of aqueous solutions were made possible by on-column focusing with partially filled loop injections. The fragmentation patterns for 2,4- and 2,6-toluene diamine (TDA) and 4,4'-methylene dianiline (MDA) were clarified by performing a hydrogen-deuterium exchange study. TDA and MDA were determined using trideuterated 2,4- and 2,6-TDA and dideuterated 4,4'-MDA as internal standards. Linear calibration graphs were obtained over the range 0.025-0.5 {mu}g mL{sup -1} with correlation coefficients >0.996 and the instrumental detection limit for each compound was <50 fmol. The stability of the amines was influenced by the matrix, so their concentrations decreased over time. Agreement was observed between the results of analyses of PUR foam extracts by HILIC-MS/MS and results obtained by ethyl chloroformate derivatisation and reversed phase (RP) liquid chromatography-mass spectrometry (LC-MS/MS). TDA was observed to be unstable in extracts of foam but not in pure solutions.

  11. Secondary Waste Cementitious Waste Form Data Package for the Integrated Disposal Facility Performance Assessment

    Energy Technology Data Exchange (ETDEWEB)

    Cantrell, Kirk J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Westsik, Joseph H. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Serne, R Jeffrey [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Um, Wooyong [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Cozzi, Alex D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2016-05-16

    A review of the most up-to-date and relevant data currently available was conducted to develop a set of recommended values for use in the Integrated Disposal Facility (IDF) performance assessment (PA) to model contaminant release from a cementitious waste form for aqueous wastes treated at the Hanford Effluent Treatment Facility (ETF). This data package relies primarily upon recent data collected on Cast Stone formulations fabricated with simulants of low-activity waste (LAW) and liquid secondary wastes expected to be produced at Hanford. These data were supplemented, when necessary, with data developed for saltstone (a similar grout waste form used at the Savannah River Site). Work is currently underway to collect data on cementitious waste forms that are similar to Cast Stone and saltstone but are tailored to the characteristics of ETF-treated liquid secondary wastes. Recommended values for key parameters to conduct PA modeling of contaminant release from ETF-treated liquid waste are provided.

  12. Digestion of frozen/thawed food waste in the hybrid anaerobic solid-liquid system.

    Science.gov (United States)

    Stabnikova, O; Liu, X Y; Wang, J Y

    2008-01-01

    The hybrid anaerobic solid-liquid (HASL) system, which is a modified two-phase anaerobic digester, is to be used in an industrial scale operation to minimize disposal of food waste at incineration plants in Singapore. The aim of the present research was to evaluate freezing/thawing of food waste as a pre-treatment for its anaerobic digestion in the HASL system. The hydrolytic and fermentation processes in the acidogenic reactor were enhanced when food waste was frozen for 24h at -20 degrees C and then thawed for 12h at 25 degrees C (experiment) in comparison with fresh food waste (control). The highest dissolved COD concentrations in the leachate from the acidogenic reactors were 16.9 g/l on day 3 in the control and 18.9 g/l on day 1 in the experiment. The highest VFA concentrations in the leachate from the acidogenic reactors were 11.7 g/l on day 3 in the control and 17.0 g/l on day 1 in the experiment. The same volume of methane was produced during 12 days in the control and 7 days in the experiment. It gave the opportunity to diminish operational time of batch process by 42%. The effect of freezing/thawing of food waste as pre-treatment for its anaerobic digestion in the HASL system was comparable with that of thermal pre-treatment of food waste at 150 degrees C for 1h. However, estimation of energy required either to heat the suspended food waste to 150 degrees C or to freeze the same quantity of food waste to -20 degrees C showed that freezing pre-treatment consumes about 3 times less energy than thermal pre-treatment.

  13. Crystalline Silicotitanate: a New Type of Ion Exchanger for Cs Removal from Liquid Waste

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The research and developments of a new type of inorganic ion exchanger, crystalline silicotitanate (CST) are reviewed.This material is stable against radiation, and the CST has high selectivity for Cs over Na, K and Rb. It performs well in acidic, neutral, and basic solutions. The results of ion exchange tests show that CST is an excellent candidate for Cs removal from high-level liquid waste.

  14. Deployment of Performance Management Methodology as part of Liquid Waste Program at Savannah River Site - 12178

    Energy Technology Data Exchange (ETDEWEB)

    Prod' homme, A.; Drouvot, O.; Gregory, J. [AREVA, Paris (France); Barnes, B.; Hodges, B.; Hart, M. [SRR, Aiken, SC (United States)

    2012-07-01

    In 2009, Savannah River Remediation LLC (SRR) assumed the management lead of the Liquid Waste (LW) Program at the Savannah River Site (SRS). The four SRR partners and AREVA, as an integrated subcontractor are performing the ongoing effort to safely and reliably: - Close High Level Waste (HLW) storage tanks; - Maximize waste throughput at the Defense Waste Processing Facility (DWPF); - Process salt waste into stable final waste form; - Manage the HLW liquid waste material stored at SRS. As part of these initiatives, SRR and AREVA deployed a performance management methodology based on Overall Equipment Effectiveness (OEE) at the DWPF in order to support the required production increase. This project took advantage of lessons learned by AREVA through the deployment of Total Productive Maintenance and Visual Management methodologies at the La Hague reprocessing facility in France. The project also took advantage of measurement data collected from different steps of the DWPF process by the SRR team (Melter Engineering, Chemical Process Engineering, Laboratory Operations, Plant Operations). Today the SRR team has a standard method for measuring processing time throughout the facility, a reliable source of objective data for use in decision-making at all levels, and a better balance between engineering department goals and operational goals. Preliminary results show that the deployment of this performance management methodology to the LW program at SRS has already significantly contributed to the DWPF throughput increases and is being deployed in the Saltstone facility. As part of the liquid waste program on Savannah River Site, SRR committed to enhance production throughput of DWPF. Beyond technical modifications implemented at different location of the facility, SRR deployed performance management methodology based on OEE metrics. The implementation benefited from the experience gained by AREVA in its own facilities in France. OEE proved to be a valuable tool in order

  15. The development of a cholesterol biosensor using a liquid crystal/aqueous interface in a SDS-included β-cyclodextrin aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Munir, Sundas; Park, Soo-Young, E-mail: psy@knu.ac.kr

    2015-09-17

    Sodium dodecyl sulphate (SDS) including β-cyclodextrin (β-CD) (β-CD{sub SDS}) was used to detect cholesterol at the 4-cyano-4′-pentylbiphenyl (5CB)/aqueous interface in transmission electron microscopy (TEM) grid cells. The β-CD acts as a host for SDS (guest). The guest SDS enclosed within the β-CD cavity was replaced with cholesterol by injecting cholesterol solution into the TEM cell at concentrations greater than 3 μM. The replacement of SDS with cholesterol was confirmed by pH measurement and high performance liquid chromatography (HPLC). The SDS excluded from the β-CD altered the planar orientation of the 5CB confined within the TEM grid cell to a homeotropic orientation. This planar-to-homeotropic transition was observed using a polarized optical microscope under crossed polarizers. This convenient TEM grid cell provides a new method for the selective detection of cholesterol without immobilization of the detecting receptors (enzyme, antibody, or aptamer) or the use of sophisticated instruments. - Highlights: • β-CD-SDS inclusion was used for the detection of cholesterol at 5CB/aqueous interface. • The SDS enclosed within the β-CD cavity was replaced by cholesterol. • The released SDS from the β-CD caused homeotropic orientation of 5CB. • The cholesterol was detected from planar-to-homeotropic transition of 5CB. • This convenient TEM grid cell provides a new method for the selective detection of cholesterol.

  16. Resistance of class C fly ash belite cement to simulated sodium sulphate radioactive liquid waste attack.

    Science.gov (United States)

    Guerrero, A; Goñi, S; Allegro, V R

    2009-01-30

    The resistance of class C fly ash belite cement (FABC-2-W) to concentrated sodium sulphate salts associated with low level wastes (LLW) and medium level wastes (MLW) is discussed. This study was carried out according to the Koch and Steinegger methodology by testing the flexural strength of mortars immersed in simulated radioactive liquid waste rich in sulphate (48,000 ppm) and demineralised water (used as a reference), at 20 degrees C and 40 degrees C over a period of 180 days. The reaction mechanisms of sulphate ion with the mortar was carried out through a microstructure study, which included the use of Scanning electron microscopy (SEM), porosity and pore-size distribution and X-ray diffraction (XRD). The results showed that the FABC mortar was stable against simulated sulphate radioactive liquid waste (SSRLW) attack at the two chosen temperatures. The enhancement of mechanical properties was a result of the formation of non-expansive ettringite inside the pores and an alkaline activation of the hydraulic activity of cement promoted by the ingress of sulphate. Accordingly, the microstructure was strongly refined.

  17. Heavy metals removal from contaminated sewage sludge by naturally fermented raw liquid from pineapple wastes.

    Science.gov (United States)

    Dacera, Dominica Del Mundo; Babel, Sandhya

    2007-01-01

    The large amount of unutilised pineapple wastes produced every year in tropical countries, particularly in Thailand, adds to the existing environmental pollution problems of the country. This study investigated the utilisation of pineapple wastes to treat another form of waste (sludge) from wastewater treatment facilities in Thailand. Laboratory scale studies were carried out to determine the potential of using naturally fermented raw liquid from pineapple wastes as a source of citric acid in the extraction of Cr, Cu, Pb, Ni and Zn from anaerobically digested sewage sludge. Results of the leaching study revealed its effectiveness in extracting Zn (at 92%) at pH 3.67 and a short leaching time of only 2 h, and Ni at almost 60% removal at the same leaching time. Chromium removal was also high at almost 75% at a longer leaching time of 11 days. Variation in metal removal efficiencies may also be attributed to the forms of metals in sludge, with metals predominantly in the exchangeable and oxidisable phases showing ease of leachability (such as Zn). Compared to citric acid, at pH approaching 4.0, naturally fermented raw liquid seemed to be more effective in the removal of Zn and Cu at the same leaching time of 2 h, and Cr at a longer leaching time of 11 days. The pineapple pulp, which is a by-product of the process, can still be used as animal feed because of its high protein content.

  18. Radioactive liquid wastes discharged to ground in the 200 Areas during 1976

    Energy Technology Data Exchange (ETDEWEB)

    Mirabella, J.E.

    1977-05-09

    An overall summary is presented giving the radioactive liquid wastes discharged to ground during 1976 and since startup (for both total and decayed depositions) within the Production and Waste Management Division control zone (200 Area plateau). Overall summaries are also presented for 200 East Area and for 200 West Area. The data contain an estimate of the radioactivity discharged to individual ponds, cribs and specific retention sites within the Production and Waste Management Division during 1976 and from startup through December 31, 1976; an estimate of the decayed activities from startup through 1976; the location and reference drawings of each disposal site; and the usage dates of each disposal site. The estimates for the radioactivity discharged and for decayed activities dicharged from startup through December 31, 1976 are based upon Item 4 of the Bibliography. The volume of liquid discharged to the ponds also includes major nonradioactive streams. The wastes discharged during 1976 to each active disposal site are detailed on a month-to-month basis, along with the monthly maximum concentration and average concentration data. An estimate of the radioactivity discharged to each active site along with the remaining decayed activities is given.

  19. Chemical constituents and antioxidant activities of waste liquid extract from Apostichopus japonicus Selenka processing

    Institute of Scientific and Technical Information of China (English)

    LI Chaofeng; LI Xiancui; LI Hong; GUO Shuju; ZHU Xiaobin

    2013-01-01

    Apostichopus japonicus Selenka is an ideal tonic food that is used traditionally in many Asian countries,and it contains many bioactive substances,such as antioxidant,antimicrobial,and anticancer materials.To convert waste liquid generated during production into a useful resource,extract from waste liquid was isolated by column chromatography and studied by the pyrogallol autoxidation and 1,10-phenanthroline-Fe2+ oxidation methods.Results show that the extract scavenged about 91% of the superoxide anion radical at a concentration of 1.4 mg/mL and 24% of the hydroxyl radical at 3.3 mg/mL.Four compounds were isolated and identified from the extract:2,4-dihydroxy-5-methyl-1,3-azine; 2,4-dihydroxy-1,3-diazine; 3-O-[β-D-quinovopranosyl-(1→2)-4-O-sodium sulfate-β-D-xylopranosyl]-holosta-9(11)-ene-3β,12t,17α-triol; and 24-ethyl-5t-cholesta-7-ene-3β-O-β-D-xylopyranoside.All of these compounds are known in A.japonicus,and were found in the waste liquid for the first time.

  20. Application of an aqueous two-phase micellar system to extract bromelain from pineapple (Ananas comosus) peel waste and analysis of bromelain stability in cosmetic formulations.

    Science.gov (United States)

    Spir, Lívia Genovez; Ataide, Janaína Artem; De Lencastre Novaes, Letícia Celia; Moriel, Patrícia; Mazzola, Priscila Gava; De Borba Gurpilhares, Daniela; Silveira, Edgar; Pessoa, Adalberto; Tambourgi, Elias Basile

    2015-01-01

    Bromelain is a set of proteolytic enzymes found in pineapple (Ananas comosus) tissues such as stem, fruit and leaves. Because of its proteolytic activity, bromelain has potential applications in the cosmetic, pharmaceutical, and food industries. The present study focused on the recovery of bromelain from pineapple peel by liquid-liquid extraction in aqueous two-phase micellar systems (ATPMS), using Triton X-114 (TX-114) and McIlvaine buffer, in the absence and presence of electrolytes CaCl2 and KI; the cloud points of the generated extraction systems were studied by plotting binodal curves. Based on the cloud points, three temperatures were selected for extraction: 30, 33, and 36°C for systems in the absence of salts; 40, 43, and 46°C in the presence of KI; 24, 27, and 30°C in the presence of CaCl2 . Total protein and enzymatic activities were analyzed to monitor bromelain. Employing the ATPMS chosen for extraction (0.5 M KI with 3% TX-114, at pH 6.0, at 40°C), the bromelain extract stability was assessed after incorporation into three cosmetic bases: an anhydrous gel, a cream, and a cream-gel formulation. The cream-gel formulation presented as the most appropriate base to convey bromelain, and its optimal storage conditions were found to be 4.0 ± 0.5°C. The selected ATPMS enabled the extraction of a biomolecule with high added value from waste lined-up in a cosmetic formulation, allowing for exploration of further cosmetic potential.

  1. Development And Initial Testing Of Off-Gas Recycle Liquid From The WTP Low Activity Waste Vitrification Process - 14333

    Energy Technology Data Exchange (ETDEWEB)

    McCabe, Daniel J.; Wilmarth, William R.; Nash, Charles A.; Taylor-Pashow, Kathryn M.; Adamson, Duane J.; Crawford, Charles L.; Morse, Megan M.

    2014-01-07

    The Waste Treatment and Immobilization Plant (WTP) process flow was designed to pre-treat feed from the Hanford tank farms, separate it into a High Level Waste (HLW) and Low Activity Waste (LAW) fraction and vitrify each fraction in separate facilities. Vitrification of the waste generates an aqueous condensate stream from the off-gas processes. This stream originates from two off-gas treatment unit operations, the Submerged Bed Scrubber (SBS) and the Wet Electrospray Precipitator (WESP). Currently, the baseline plan for disposition of the stream from the LAW melter is to recycle it to the Pretreatment facility where it gets evaporated and processed into the LAW melter again. If the Pretreatment facility is not available, the baseline disposition pathway is not viable. Additionally, some components in the stream are volatile at melter temperatures, thereby accumulating to high concentrations in the scrubbed stream. It would be highly beneficial to divert this stream to an alternate disposition path to alleviate the close-coupled operation of the LAW vitrification and Pretreatment facilities, and to improve long-term throughput and efficiency of the WTP system. In order to determine an alternate disposition path for the LAW SBS/WESP Recycle stream, a range of options are being studied. A simulant of the LAW Off-Gas Condensate was developed, based on the projected composition of this stream, and comparison with pilot-scale testing. The primary radionuclide that vaporizes and accumulates in the stream is Tc-99, but small amounts of several other radionuclides are also projected to be present in this stream. The processes being investigated for managing this stream includes evaporation and radionuclide removal via precipitation and adsorption. During evaporation, it is of interest to investigate the formation of insoluble solids to avoid scaling and plugging of equipment. Key parameters for radionuclide removal include identifying effective precipitation or ion

  2. Adsorption-desorption characteristics of phenol and reactive dyes from aqueous solution on mesoporous activated carbon prepared from waste tires.

    Science.gov (United States)

    Tanthapanichakoon, W; Ariyadejwanich, P; Japthong, P; Nakagawa, K; Mukai, S R; Tamon, H

    2005-04-01

    Liquid-phase adsorption-desorption characteristics and ethanol regeneration efficiency of an activated carbon prepared from waste tires and a commercial activated carbon were investigated. Water vapor adsorption experiments reveal that both activated carbons showed hydrophobic surface characteristics. Adsorption experiments reveal that the prepared activated carbon possessed comparable phenol adsorption capacity as the commercial one but clearly larger adsorption capacity of two reactive dyes, Black 5 and Red 31. It was ascertained that the prepared activated carbon exhibited less irreversible adsorption of phenol and the two dyes than its commercial counterpart. Moreover, ethanol regeneration efficiency of the prepared AC saturated with either dye was higher than that of the commercial AC. Because of its superior liquid-phase adsorption-desorption characteristics as well as higher ethanol regeneration efficiency, the prepared activated carbon is more suitable for wastewater treatment, especially for adsorbing similarly bulky adsorbates.

  3. Aqueous ionic liquid based ultrasonic assisted extraction of four acetophenones from the Chinese medicinal plant Cynanchum bungei Decne.

    Science.gov (United States)

    Sun, Yinshi; Liu, Zhengbo; Wang, Jianhua; Yang, Saifei; Li, Baiqing; Xu, Ning

    2013-01-01

    In this study, an aqueous ionic liquid based ultrasonic assisted extraction (ILUAE) method for the extraction of the four acetophenones, namely 4-hydroxyacetophenone (1), 2,5-dihydroxyacetophenone (2), baishouwubenzophenone (3) and 2,4-dihydroxyacetophenone (4) from the Chinese medicinal plant Cynanchum bungei was developed. Three kinds of aqueous l-alkyl-3-methylimidazolium ionic liquids with different anion and alkyl chain were investigated. The results indicated that ionic liquids (ILs) showed remarkable effects on the extraction efficiency of acetophenones. In addition, the ILUAE, including several ultrasonic parameters, such as the ILs concentration, solvent to solid ratio, power, particle size, temperature, and extraction time have been optimized. Under these optimal conditions (e.g., with 0.6M [C(4)MIM]BF(4), solvent to solid ratio of 35:1, power of 175 W, particle size of 60-80 mesh, temperature of 25 ° C and time of 50 min), this approach gained the highest extraction yields of four acetophenones 286.15, 21.65, 632.58 and 205.38 μg/g, respectively. The proposed approach has been evaluated by comparison with the conventional heat-reflux extraction (HRE) and regular UAE. The results indicated that ILUAE is an alternative method for extracting acetophenones from C. bungei.

  4. Utilization of various agricultural wastes for activated carbon preparation and application for the removal of dyes and metal ions from aqueous solutions.

    Science.gov (United States)

    Kadirvelu, K; Kavipriya, M; Karthika, C; Radhika, M; Vennilamani, N; Pattabhi, S

    2003-03-01

    Activated carbons were prepared from the agricultural solid wastes, silk cotton hull, coconut tree sawdust, sago waste, maize cob and banana pith and used to eliminate heavy metals and dyes from aqueous solution. Adsorption of all dyes and metal ions required a very short time and gave quantitative removal. Experimental results show all carbons were effective for the removal of pollutants from water. Since all agricultural solid wastes used in this investigation are freely, abundantly and locally available, the resulting carbons are expected to be economically viable for wastewater treatment.

  5. Analysis of an explosion accident of nitrogen trichloride in a waste liquid containing ammonium ion and platinum black.

    Science.gov (United States)

    Okada, Ken; Akiyoshi, Miyako; Ishizaki, Keiko; Sato, Hiroyasu; Matsunaga, Takehiro

    2014-08-15

    Five liters of sodium hypochlorite aqueous solution (12 mass%) was poured into 300 L of liquid waste containing ammonium ion of about 1.8 mol/L in a 500 L tank in a plant area; then, two minutes later the solution exploded with a flash on March 30th, 2005. The tank cover, the fluorescent lamp and the air duct were broken by the blast wave. Thus, we have conducted 40 runs of laboratory-scale explosion tests under various conditions (solution concentrations of (NH4)2SO4 and NaClO, temperatures, Pt catalysts, pH, etc.) to investigate the causes for such an explosion. When solutions of ammonium sulfate and sodium hypochlorite are mixed in the presence of platinum black, explosions result. This is ascribable to the formation of explosive nitrogen trichloride (NCl3). In the case where it is necessary to mix these 2 solutions (ammonium sulfate and sodium hypochlorite) in the presence of platinum black, the following conditions would reduce a probability of explosion; the initial concentration of NH4(+) should be less than 3 mol/L and the pH should be higher than 6. The hypochlorite solution (in 1/10 in volume) to be added at room temperature is recommended to be less than 0.6 mol/L.

  6. Surfactant and Gelation Properties of Acetylsalicylate Based Room Temperature Ionic Liquid in Aqueous Media.

    Science.gov (United States)

    Sastry, Nandhibatla V; Singh, Dipak K

    2016-10-04

    An amphiphilic room temperature ionic liquid (RTIL) containing acetylsalicylate anion of type 1-dodecyl-1-methylpiperidinium acetylsalicylate, [C12mpip][AcSa], is synthesized from the precursor [C12mpip][Cl] by an ion exchange process. The sample is characterized, and its surface active and aggregation behavior in water has been studied and explained. The critical aggregation concentrations (CACs) are determined by a variety of methods, namely, electrical conductivity, surface tension, steady state florescence, and isothermal titration calorimetry (ITC) at different temperatures. As compared to its precursor, [C12mpip][AcSa] has low CAC values, indicating enhanced favorable interactions between the [alkylmpip](+) cation···bulky [AcSa](-) anion and also hydrogen bonding of both of the ions with water. The free energy of aggregation ΔG(0)a is always negative, and both enthalpy and entropy of aggregation drive the aggregation process. The micelle-like aggregates are ellipsoidal in shape. The aggregation numbers are determined from translational diffusion coefficients and florescence quenching measurements. Aggregates of [C12mpip][AcSa] are larger than those of its precursor IL with chloride anion. Therefore, it is evident that the close interactions between the ion pairs of [C12mpip](+)···[AcSa](-) facilitate packing of more molecules in an aggregate. The steady state and oscillatory rheology measurements in aqueous solutions consisting of mixtures of [C12mpip][AcSa] and sodium salicylate (SS), an hydrotope additive, were carried out. The analysis of zero shear viscosity and moduli properties as a function of concentration and temperature reveals that the addition of SS promotes the growth of small ellipsoid aggregates into large worm-like structures with a typical viscoelastic gel behavior. The moduli properties vs temperature profiles are complex and no hysteresis was produced in heating and cooling modes, suggesting the thermoirreversibile and complex nature

  7. Removal of phenol from aqueous solution and resin manufacturing industry wastewater using an agricultural waste: rubber seed coat.

    Science.gov (United States)

    Rengaraj, S; Moon, Seung-Hyeon; Sivabalan, R; Arabindoo, Banumathi; Murugesan, V

    2002-01-28

    Activated carbon prepared from rubber seed coat (RSCC), an agricultural waste by-product, has been used for the adsorption of phenol from aqueous solution. In this work, adsorption of phenol on rubber seed coat activated carbon has been studied by using batch and column studies. The equilibrium adsorption level was determined to be a function of the solution pH, adsorbent dosage and contact time. The equilibrium adsorption capacity of rubber seed coat activated carbon for phenol removal was obtained by using linear Freundlich isotherm. The adsorption of phenol on rubber seed coat activated carbon follows first order reversible kinetics. The suitability of RSCC for treating phenol based resin manufacturing industry wastewater was also tested. A comparative study with a commercial activated carbon (CAC) showed that RSCC is 2.25 times more efficient compared to CAC based on column adsorption study for phenolic wastewater treatment.

  8. Simultaneous production of high-quality water and electrical power from aqueous feedstock’s and waste heat by high-pressure membrane distillation

    NARCIS (Netherlands)

    Kuipers, N.J.M.; Hanemaaijer, J.H.; Brouwer, H.; Medevoort, J. van; Jansen, A.; Altena, F.; Vleuten, P. van der; Bak, H.

    2015-01-01

    A new membrane distillation (MD) concept (MemPower) has been developed for the simultaneous production of high-quality water from various aqueous feedstocks with cogeneration of mechanical power (electricity). Driven by low-grade heat (waste, solar, geothermal, etc.) a pressurized distillate can be

  9. BioWaste-to-Liquid. An ecologic-economic consideration of pyrolysis oil based on biogenic residual materials and wastes; BioWaste-to-Liquid. Oekologisch-oekonomische Betrachtung von Pyrolyseoel auf Basis biogener Rest- und Abfallstoffe

    Energy Technology Data Exchange (ETDEWEB)

    Liemen, Franziska; Zech, Konstantin; Kroeger, Michael [DBFZ Deutsches Biomasseforschungszentrum gemeinnuetzige GmbH, Leipzig (Germany)

    2012-07-01

    The joint research project BioWaste-to-Liquid, which is carried out by Deutsches BiomasseForschungsZentrum (DBFZ) and Karlsruhe Institute of Technology (KIT), focuses on the provision of alternative fuels by means of fast pyrolysis. Alongside the various tests and technical analyses, an ecologic and economic assessment was carried out, that examines the performance of different raw materials in terms of GHG-emissions and production costs. The herein examined raw materials were Rape straw, Sunflower straw, residues of corn harvesting, hay, waste wood, bark and driftwood from river Rhine. The results show a good performance of waste wood and draft wood both in ecologic and economic terms, whilst especially Sunflower straw can be considered rather unsuitable since it is particularly affected by the negative effects of the compensatory fertilization. The other raw materials perform varyingly in the ecologic and economic assessments. (orig.)

  10. Nano-cerium vanadate: A novel inorganic ion exchanger for removal of americium and uranium from simulated aqueous nuclear waste

    Energy Technology Data Exchange (ETDEWEB)

    Banerjee, Chayan; Dudwadkar, Nilesh [Fuel Reprocessing Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Tripathi, Subhash Chandra, E-mail: sctri001@gmail.com [Fuel Reprocessing Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Gandhi, Pritam Maniklal [Fuel Reprocessing Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Grover, Vinita [Waste Management Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Kaushik, Chetan Prakash [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Tyagi, Avesh Kumar, E-mail: aktyagi@barc.gov.in [Waste Management Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)

    2014-09-15

    Highlights: • Template free, low temperature synthesis of CeVO{sub 4} nanopowders. • Thermodynamically and kinetically favourable uptake of Am(III) and U(VI) exhibited. • K{sub d} and ΔG° values for Am(III) and U(VI) uptake in pH 1–6 are reported. • Interdiffusion coefficients and zeta potential values in pH 1–6 are reported. • Possible application in low level aqueous nuclear waste remediation. - Abstract: Cerium vanadate nanopowders were synthesized by a facile low temperature co-precipitation method. The product was characterized by X-ray diffraction and transmission electron microscopy and found to consist of ∼25 nm spherical nanoparticles. The efficiency of these nanopowders for uptake of alpha-emitting radionuclides {sup 233}U (4.82 MeV α) and {sup 241}Am (5.49 MeV α, 60 keV γ) has been investigated. Thermodynamically and kinetically favorable uptake of these radionuclides resulted in their complete removal within 3 h from aqueous acidic feed solutions. The uptake capacity was observed to increase with increase in pH as the zeta potential value decreased with the increase in pH but effect of ionic strength was insignificant. Little influence of the ions like Sr{sup 2+}, Ru{sup 3+}, Fe{sup 3+}, etc., in the uptake process indicated CeVO{sub 4} nanopowders to be amenable for practical applications. The isotherms indicated predominant uptake of the radioactive metal ions in the solid phase of the exchanger at lower feed concentrations and linear Kielland plots with positive slopes indicated favorable exchange of the metal ions with the nanopowder. Performance comparison with the other sorbents reported indicated excellent potential of nano-cerium vanadate for removing americium and uranium from large volumes of aqueous acidic solutions.

  11. Extended UNIQUAC Model for Correlation and Prediction of Vapor-Liquid-Liquid-Solid Equilibria in Aqueous Salt Systems Containing Non-Electrolytes. Part B. Alcohol (Ethanol, Propanols, Butanols) - Water-salt systems

    DEFF Research Database (Denmark)

    Thomsen, Kaj; Iliuta, Maria Cornelia; Rasmussen, Peter

    2004-01-01

    -Redlich-Kwong equation of state. The model only requires binary, temperature-dependent interaction parameters. It has previously been used to describe the excess Gibbs energy for aqueous electrolyte mixtures and aqueous electrolyte systems containing methanol. It has been found to be an adequate model for representing...... solid-liquid-vapor equilibrium and thermal property data for strongly non-ideal systems. In this work, the model is extended to aqueous salt systems containing higher alcohols. The calculations are based on an extensive database consisting of salt solubility data, vapor liquid equilibrium data...

  12. Application of elevated temperature-dispersive liquid-liquid microextraction for determination of organophosphorus pesticides residues in aqueous samples followed by gas chromatography-flame ionization detection.

    Science.gov (United States)

    Farajzadeh, Mir Ali; Afshar Mogaddam, Mohammad Reza; Rezaee Aghdam, Samaneh; Nouri, Nina; Bamorrowat, Mahdi

    2016-12-01

    In the present study, an elevated temperature, dispersive, liquid-liquid microextraction/gas chromatography-flame ionization detection was investigated for the determination, pre-concentration, and extraction of six organophosphorus pesticides (malathion, phosalone, dichlorvos, diazinon, profenofos, and chlorpyrifos) residues in fruit juice and aqueous samples. A mixture of 1,2-dibromoethane (extraction solvent) and dimethyl sulfoxide (disperser solvent) was injected rapidly into the sample solution heated at an elevated temperature. Analytical parameters, including enrichment factors (1600-2075), linearity (r>0.994), limits of detection (0.82-2.72ngmL(-1)) and quantification (2.60-7.36ngmL(-1)), relative standard deviations (<7%) and extraction recoveries (64-83%), showed the high efficiency of the method developed for analysis of the target analytes. The proposed procedure was used effectively to analyse selected analytes in river water and fruit juice, and diazinon was found at ngmL(-1) concentrations in apple juice.

  13. Determination of sunset yellow and tartrazine in food samples by combining ionic liquid-based aqueous two-phase system with high performance liquid chromatography.

    Science.gov (United States)

    Sha, Ou; Zhu, Xiashi; Feng, Yanli; Ma, Weixing

    2014-01-01

    We proposed a simple and effective method, by coupling ionic liquid-based aqueous two-phase systems (IL-ATPSs) with high performance liquid chromatography (HPLC), for the analysis of determining tartrazine and sunset yellow in food samples. Under the optimized conditions, IL-ATPSs generated an extraction efficiency of 99% for both analytes, which could then be directly analyzed by HPLC without further treatment. Calibration plots were linear in the range of 0.01-50.0 μg/mL for both Ta and SY. The limits of detection were 5.2 ng/mL for Ta and 6.9 ng/mL for SY. This method proves successful for the separation/analysis of tartrazine and sunset yellow in soft drink sample, candy sample, and instant powder drink and leads to consistent results as obtained from the Chinese national standard method.

  14. Determination of Sunset Yellow and Tartrazine in Food Samples by Combining Ionic Liquid-Based Aqueous Two-Phase System with High Performance Liquid Chromatography

    Directory of Open Access Journals (Sweden)

    Ou Sha

    2014-01-01

    Full Text Available We proposed a simple and effective method, by coupling ionic liquid-based aqueous two-phase systems (IL-ATPSs with high performance liquid chromatography (HPLC, for the analysis of determining tartrazine and sunset yellow in food samples. Under the optimized conditions, IL-ATPSs generated an extraction efficiency of 99% for both analytes, which could then be directly analyzed by HPLC without further treatment. Calibration plots were linear in the range of 0.01–50.0 μg/mL for both Ta and SY. The limits of detection were 5.2 ng/mL for Ta and 6.9 ng/mL for SY. This method proves successful for the separation/analysis of tartrazine and sunset yellow in soft drink sample, candy sample, and instant powder drink and leads to consistent results as obtained from the Chinese national standard method.

  15. Radiation-induced protein fragmentation and inactivation in liquid and solid aqueous solutions. Role of OH and electrons

    Energy Technology Data Exchange (ETDEWEB)

    Audette-Stuart, Marilyne [Atomic Energy of Canada Limited, CANDU Life Sciences Center, Chalk River Laboratories, Chalk River Ont., K0J 1J0 (Canada); Houee-Levin, Chantal [Laboratoire de Chimie Physique, UMR-8000 CNRS-Universite Paris XI, Centre Universitaire, F-91405 Orsay Cedex (France)]. E-mail: chantal.houee-levin@lcp.u-psud.fr; Potier, Michel [Service de genetique medicale, Hopital Sainte-Justine, Universite de Montreal, Montreal Que., H3 T 1C5 (Canada)

    2005-02-01

    Irradiation of proteins in diluted liquid aqueous solutions produces cleavages and polymerizations of the peptidic chains. In frozen solutions, fragmentation is observed but polymerization products are absent. Loss of activity occurs in both cases. In the solid state, yields of fragmentation do not vary with the quantity of water. The use of scavengers indicates that hydroxyl radical does not contribute significantly to fragmentation and to inactivation in the solid state. Electrons within the water molecules closely associated with the protein are involved in the processes leading to protein fragmentation.

  16. LOW LEVEL LIQUID RADIOACTIVE WASTE TREATMENT AT MURMANSK, RUSSIA: FACILITY UPGRADE AND EXPANSION

    Energy Technology Data Exchange (ETDEWEB)

    BOWERMAN,B.; CZAJKOWSKI,C.; DYER,R.S.; SORLIE,A.

    2000-03-01

    Today there exist many almost overfilled storage tanks with liquid radioactive waste in the Russian Federation. This waste was generated over several years by the civil and military utilization of nuclear power. The current waste treatment capacity is either not available or inadequate. Following the London Convention, dumping of the waste in the Arctic seas is no longer an alternative. Waste is being generated from today's operations, and large volumes are expected to be generated from the dismantling of decommissioned nuclear submarines. The US and Norway have an ongoing co-operation project with the Russian Federation to upgrade and expand the capacity of a treatment facility for low level liquid waste at the RTP Atomflot site in Murmansk. The capacity will be increased from 1,200 m{sup 3}/year to 5,000 m{sup 3} /year. The facility will also be able to treat high saline waste. The construction phase will be completed the first half of 1998. This will be followed by a start-up and a one year post-construction phase, with US and Norwegian involvement for the entire project. The new facility will consist of 9 units containing various electrochemical, filtration, and sorbent-based treatment systems. The units will be housed in two existing buildings, and must meet more stringent radiation protection requirements that were not enacted when the facility was originally designed. The US and Norwegian technical teams have evaluated the Russian design and associated documentation. The Russian partners send monthly progress reports to US and Norway. Not only technical issues must be overcome but also cultural differences resulting from different methods of management techniques. Six to eight hour time differentials between the partners make real time decisions difficult and relying on electronic age tools becomes extremely important. Language difficulties is another challenge that must be solved. Finding a common vocabulary, and working through interpreters make the

  17. Aqueous two-phase based on ionic liquid liquid-liquid microextraction for simultaneous determination of five synthetic food colourants in different food samples by high-performance liquid chromatography.

    Science.gov (United States)

    Sha, Ou; Zhu, Xiashi; Feng, Yanli; Ma, Weixing

    2015-05-01

    A rapid and effective method of aqueous two-phase systems based on ionic liquid microextraction for the simultaneous determination of five synthetic food colourants (tartrazine, sunset yellow, amaranth, ponceau 4R and brilliant blue) in food samples was established. High-performance liquid chromatography coupled with an ultraviolet detector of variable wavelength was used for the determinations. 1-alkyl-3-methylimidazolium bromide was selected as the extraction reagent. The extraction efficiency of the five colourants in the proposed system is influenced by the types of salts, concentrations of salt and [CnMIM]Br, as well as the extracting time. Under the optimal conditions, the extraction efficiencies for these five colourants were above 95%. The phase behaviours of aqueous two-phase system and extraction mechanism were investigated by UV-vis spectroscopy. This method was applied to the analysis of the five colourants in real food samples with the detection limit of 0.051-0.074 ng/mL. Good spiked recoveries from 93.2% to 98.9% were obtained.

  18. Detection of Clostridium botulinum in liquid manure and biogas plant wastes.

    Science.gov (United States)

    Neuhaus, Jürgen; Schrödl, Wieland; Shehata, Awad A; Krüger, Monika

    2015-09-01

    Biogas plants have been considered as a source for possible amplification and distribution of pathogenic bacteria capable of causing severe infections in humans and animals. Manure and biogas wastes could be sources for spore-forming bacteria such as Clostridium botulinum. In the present study, 24 liquid manure and 84 biogas waste samples from dairies where the majority of the cows suffered from chronic botulism were investigated for the presence of botulinum neurotoxins (BoNT) and C. botulinum spores. The prevalence of BoNT/A, B, C, D, and E in biogas wastes was 16.6, 8.3, 10.7, 7.1, and 10.8 %, respectively, while in manure, the prevalence was 0.0, 0.0, 0.0, 8.3, and 4.1 %, respectively. After enrichment of samples in reinforced cultural medium, they were tested for C. botulinum BoNT/A, B, C, D, and E using ELISA (indirect C. botulinum detection). The prevalence of C. botulinum type A, B, C, D, and E samples in biogas wastes was 20.2, 15.5, 19, 10.7, and 34.8 %, respectively, while the prevalence in liquid manure was 0.0, 0.0, 0.0, 8.3, and 12.5 %, respectively. In conclusion, the occurrence of BoNT and C. botulinum spores in biogas waste of diseased animals indicates an increased and underestimated hygienic risk. Application of digestates from biogas fermentations as fertilizers could lead to an accumulation of long lifespan spores in the environment and could be a possible health hazard.

  19. Removal of Cu(II Ions from Aqueous Solutions by Adsorption Onto Activated Carbon Derived From Olive Waste Cakes

    Directory of Open Access Journals (Sweden)

    Hesham G. Ibrahim

    2016-04-01

    Full Text Available This paper studied the ability of using local activated carbon (LAC derived from olive waste cakes as an adsorbent for the removal of Cu(II ions from aqueous solution by batch operation. Various operating parameters such as solution pH, adsorbent dosage, initial metal ions concentration, and equilibrium contact time have been studied. The results indicated that the adsorption of Cu(II increased with the increasing pH, and the optimum solution pH for the adsorption of Cu(II was found to be 5. The adsorption process increases with increasing dosage of LAC, also the amount of Cu(II removed changes with Cu(II initial concentration and contact time. Adsorption was rapid and occurred within 25 min. for Cu(II concentration range from 60 to 120 mg/l isothermally at 30±1 oC. Maximum adsorption occurs at Cu(II initial concentration lesser than 100 mg/l by using adsorbent dosage (1.2 g/l. The equilibrium adsorption data for Cu(II were fitted well with the Langmuir and Freundlich adsorption isotherm models. The maximum adsorption capacity of LAC was found to be 106.383 mg/g. So, the results indicated the suitability use of the activated carbon derived from olive waste cakes (LAC as low cost and natural material for reliable removal of Cu(II from water and wastewater effluents.

  20. Utilization of waste phosphogypsum to prepare hydroxyapatite nanoparticles and its application towards removal of fluoride from aqueous solution.

    Science.gov (United States)

    Zhang, Deyi; Luo, Heming; Zheng, Liwen; Wang, Kunjie; Li, Hongxia; Wang, Yi; Feng, Huixia

    2012-11-30

    In the present study, waste phosphogypsum (PG) was utilized firstly to prepare hydroxyapatite nanoparticles (nHAp) via microwave irradiation technology. The nHAp derived from PG exhibited a hexagonal structure with the particle size about 20 nm × 60 nm and high purity. Meanwhile, the adsorption behaviour of fluoride onto the nHAp derived from PG was investigated to evaluate the potential application of this material for the treatment of the wastewater polluted with fluoride. The results indicate that the nHAp derived from PG can be used as an efficient adsorbent for the removal of fluoride from aqueous solution. The maximum adsorption capacities calculated from Langmuir-Freundlich model were 19.742, 26.108, 36.914 and 40.818 mg F(-)/g nHAp for 298, 308, 318 and 328 K, respectively. The pseudo-second order kinetic model was found to provide the best correlation of the used experimental data compared to the pseudo-first order and the adsorption isotherm could be well defined by Langmuir-Freundlich equation. The adsorption mechanism investigation shows that electrostatic interaction and hydrogen bond are the main driving force for fluoride uptake onto nHAp derived from waste PG.

  1. Investigation on the extraction of strontium ions from aqueous phase using crown ether-ionic liquid systems

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The extraction of strontium ions using DCH18C6 as the extractant and various ionic liquids(ILs) as solvents has been investigated.The distribution ratio of Sr2+ can reach as high as 103 under certain conditions,much larger than that in DCH18C6/n-octanol system.The extraction capacity depends greatly on the structure of ionic liquids.In Ils-based extraction systems,the extraction efficiency of strontium ions is reduced by increasing the concentration of nitric acid and can also be influenced directly by the presence of Na+ and K+ in the aqueous phase.It is confirmed that the extraction proceeds mainly via a cation-exchange mechanism.

  2. Investigation on the extraction of strontium ions from aqueous phase using crown ether-ionic liquid systems

    Institute of Scientific and Technical Information of China (English)

    XU Chao; SHEN XingHai; CHEN QingDe; GAO HongCheng

    2009-01-01

    The extraction of strontium ions using DCH18C6 as the extractant and various ionic liquids (Ils) as solvents has been investigated.The distribution ratio of Sr~(2+) can reach as high as 10~3 under certain conditions,much larger than that in DCH18C6/n-octanol system.The extraction capacity depends greatly on the structure of ionic liquids.In Ils-based extraction systems,the extraction efficiency of strontium ions is reduced by increasing the concentration of nitric acid and can also be influenced directly by the presence of Na~+ and K~+ in the aqueous phase.It is confirmed that the extraction proceeds mainly via a cation-exchange mechanism.

  3. Utilization of waste phosphogypsum to prepare hydroxyapatite nanoparticles and its application towards removal of fluoride from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Deyi, E-mail: xixizhang@lut.cn [College of Petrochemical Technology, Lanzhou University of Technology, Lanzhou 730050 (China); State Key Laboratory of Gansu Advanced Non-ferrous Metal Materials, Lanzhou University of Technology, Lanzhou 730050 (China); Luo, Heming; Zheng, Liwen; Wang, Kunjie; Li, Hongxia; Wang, Yi; Feng, Huixia [College of Petrochemical Technology, Lanzhou University of Technology, Lanzhou 730050 (China)

    2012-11-30

    Highlights: Black-Right-Pointing-Pointer A novel approach on recycle of waste phosphogypsum was exploited. Black-Right-Pointing-Pointer Phosphogypsum was utilized to prepare hydroxyapatite nanoparticles with high purity. Black-Right-Pointing-Pointer nHAp derived from PG exhibits excellent adsoprtion capacity for fluoride. Black-Right-Pointing-Pointer Fluoride adsorbs onto nHAp mainly by electrostatic interaction and hydrogen bond. - Abstract: In the present study, waste phosphogypsum (PG) was utilized firstly to prepare hydroxyapatite nanoparticles (nHAp) via microwave irradiation technology. The nHAp derived from PG exhibited a hexagonal structure with the particle size about 20 nm Multiplication-Sign 60 nm and high purity. Meanwhile, the adsorption behaviour of fluoride onto the nHAp derived from PG was investigated to evaluate the potential application of this material for the treatment of the wastewater polluted with fluoride. The results indicate that the nHAp derived from PG can be used as an efficient adsorbent for the removal of fluoride from aqueous solution. The maximum adsorption capacities calculated from Langmuir-Freundlich model were 19.742, 26.108, 36.914 and 40.818 mg F{sup -}/g nHAp for 298, 308, 318 and 328 K, respectively. The pseudo-second order kinetic model was found to provide the best correlation of the used experimental data compared to the pseudo-first order and the adsorption isotherm could be well defined by Langmuir-Freundlich equation. The adsorption mechanism investigation shows that electrostatic interaction and hydrogen bond are the main driving force for fluoride uptake onto nHAp derived from waste PG.

  4. PEG-salt aqueous two-phase systems: an attractive and versatile liquid-liquid extraction technology for the downstream processing of proteins and enzymes.

    Science.gov (United States)

    Glyk, Anna; Scheper, Thomas; Beutel, Sascha

    2015-08-01

    Nowadays, there is an increasing demand to establish new feasible, efficient downstream processing (DSP) techniques in biotechnology and related fields. Although several conventional DSP technologies have been widely employed, they are usually expensive and time-consuming and often provide only low recovery yields. Hence, the DSP is one major bottleneck for the commercialization of biological products. In this context, polyethylene glycol (PEG)-salt aqueous two-phase systems (ATPS) represent a promising, efficient liquid-liquid extraction technology for the DSP of various biomolecules, such as proteins and enzymes. Furthermore, ATPS can overcome the limitations of traditional DSP techniques and have gained importance for applications in several fields of biotechnology due to versatile advantages over conventional DSP methods, such as biocompatibility, technical simplicity, and easy scale-up potential. In the present review, various practical applications of PEG-salt ATPS are presented to highlight their feasibility to operate as an attractive and versatile liquid-liquid extraction technology for the DSP of proteins and enzymes, thus facilitating the approach of new researchers to this technique. Thereby, single- and multi-stage extraction, several process integration methods, as well as large-scale extraction and purification of proteins regarding technical aspects, scale-up, recycling of process chemicals, and economic aspects are discussed.

  5. Liquid and Gaseous Waste Operations Department annual operating report, CY 1992

    Energy Technology Data Exchange (ETDEWEB)

    Gillespie, M.A.; Maddox, J.J.; Scott, C.B.

    1993-03-01

    A total of 6.05 x 10{sup 7} gal of liquid waste was decontaminated by the Process Waste Treatment Plant (PWTP) ion exchange system during CY 1992. This averaged to 115 gpm throughout the year. When necessary, a wastewater sidestream of 50--80 gpm was treated through the use of a natural zeolite treatment system. An additional 8.00 x 10{sup 6} gal (average of 15 gpm throughout the year) were treated by the zeolite system. Therefore, the average total flow treated at the PWTP for CY 1992 was 130 gpm. In mid-June, the zeolite system was repiped to allow it the capability to treat the ion exchange system`s discharge due to rising Cs problems in the wastewater. While being used to treat the ion exchange system`s discharge, it cannot treat a sidestream of wastewater. During the year, the regeneration of the cation exchange resins resulted in the generation of 7.83 x 10{sup 3} gal of liquid low-level waste (LLLW) concentrate and 1.15 x 10{sup 4} gal of LLLW evaporator feed. The head-end softening process (precipitation/clarification) generated 604 drums (4.40 x 10{sup 3} ft{sup 3}) of solid low-level waste sludge. The zeolite treatment system generated approximately 8.40 x 10{sup 2} ft{sup 3} of spent zeolite resin, which was turned over to the Solid Waste Operations Department for disposal. See Table 1 for a monthly summary of activities at the PWTP. Figures 1, 2, 3, and 4 show a comparison of operations at the PWTP in 1992 with previous years. Figure 5 shows a comparison of annual rainfall at Oak Ridge National Laboratory (ORNL) since 1987. A total of 1.55 x 10{sup 8} gal of liquid waste (average of 294 gpm throughout the year) was treated at the Nonradiological Wastewater Treatment Plant (NRWTP). Of this amount, 1.40 x 10{sup 7} gal were treated by the precipitation/clarification process for removal of heavy metals. Twenty-five boxes (1.60 x 10{sup 3} ft{sup 3}) of solid sludge generated by the precipitation/clarification process were removed from the filter press room.

  6. Liquid and Gaseous Waste Operations Department annual operating report, CY 1992

    Energy Technology Data Exchange (ETDEWEB)

    Gillespie, M.A.; Maddox, J.J.; Scott, C.B.

    1993-03-01

    A total of 6.05 x 10[sup 7] gal of liquid waste was decontaminated by the Process Waste Treatment Plant (PWTP) ion exchange system during CY 1992. This averaged to 115 gpm throughout the year. When necessary, a wastewater sidestream of 50--80 gpm was treated through the use of a natural zeolite treatment system. An additional 8.00 x 10[sup 6] gal (average of 15 gpm throughout the year) were treated by the zeolite system. Therefore, the average total flow treated at the PWTP for CY 1992 was 130 gpm. In mid-June, the zeolite system was repiped to allow it the capability to treat the ion exchange system's discharge due to rising Cs problems in the wastewater. While being used to treat the ion exchange system's discharge, it cannot treat a sidestream of wastewater. During the year, the regeneration of the cation exchange resins resulted in the generation of 7.83 x 10[sup 3] gal of liquid low-level waste (LLLW) concentrate and 1.15 x 10[sup 4] gal of LLLW evaporator feed. The head-end softening process (precipitation/clarification) generated 604 drums (4.40 x 10[sup 3] ft[sup 3]) of solid low-level waste sludge. The zeolite treatment system generated approximately 8.40 x 10[sup 2] ft[sup 3] of spent zeolite resin, which was turned over to the Solid Waste Operations Department for disposal. See Table 1 for a monthly summary of activities at the PWTP. Figures 1, 2, 3, and 4 show a comparison of operations at the PWTP in 1992 with previous years. Figure 5 shows a comparison of annual rainfall at Oak Ridge National Laboratory (ORNL) since 1987. A total of 1.55 x 10[sup 8] gal of liquid waste (average of 294 gpm throughout the year) was treated at the Nonradiological Wastewater Treatment Plant (NRWTP). Of this amount, 1.40 x 10[sup 7] gal were treated by the precipitation/clarification process for removal of heavy metals. Twenty-five boxes (1.60 x 10[sup 3] ft[sup 3]) of solid sludge generated by the precipitation/clarification process were removed from the filter

  7. Development of a new dispersive liquid-liquid microextraction method in a narrow-bore tube for preconcentration of triazole pesticides from aqueous samples.

    Science.gov (United States)

    Farajzadeh, Mir Ali; Djozan, Djavanshir; Khorram, Parisa

    2012-02-03

    In the present work a new, simple, rapid and environmentally friendly dispersive liquid-liquid microextraction (DLLME) method has been developed for extraction/preconcentration of some triazole pesticides in aqueous samples and in grape juice. The extract was analyzed with gas chromatography-flame ionization detection (GC-FID) or gas chromatography-mass spectrometry (GC-MS). The DLLME method was performed in a narrow-bore tube containing aqueous sample. Acetonitrile and a mixture of n-hexanol and n-hexane (75:25, v/v) were used as disperser and extraction solvents, respectively. The effect of several factors that influence performance of the method, including the chemical nature and volume of the disperser and extraction solvents, number of extraction, pH and salt addition, were investigated and optimized. Figures of merit such as linearity (r(2)>0.995), enrichment factors (EFs) (263-380), limits of detection (0.3-5 μg L(-1)) and quantification (0.9-16.7 μg L(-1)), and relative standard deviations (3.2-5%) of the proposed method were satisfactory for determination of the model analytes. The method was successfully applied for determination of target pesticides in grape juice and good recoveries (74-99%) were achieved for spiked samples. As compared with the conventional DLLME, the proposed DLLME method showed higher EFs and less environmental hazards with no need for centrifuging.

  8. Characterization of electrochemically deposited films from aqueous and ionic liquid cobalt precursors toward hydrogen evolution reactions

    Science.gov (United States)

    Dushatinski, Thomas; Huff, Clay; Abdel-Fattah, Tarek M.

    2016-11-01

    Electrodepositions of cobalt films were achieved using an aqueous or an ethylene glycol based non-aqueous solution containing choline chloride (vitamin B4) with cobalt chloride hexahydrate precursor toward hydrogen evolution reactions from sodium borohydride (NaBH4) as solid hydrogen feedstock (SHF). The resulting cobalt films had reflectivity at 550 nm of 2.2% for aqueously deposited films (ACoF) and 1.3% for non-aqueously deposited films (NCoF). Surface morphology studied by scanning electron microscopy showed a positive correlation between particle size and thickness. The film thicknesses were tunable between >100 μm and reactions over a 1 cm2 catalytic surface with aqueous NaBH4 solutions generated rate constants (K) = equal to 4.9 × 10-3 min-1, 4.6 × 10-3 min-1, and 3.3 × 10-3 min-1 for ACoF, NCoF, and copper substrate respectively.

  9. Liquid digestate from anaerobic treatment of source-separated household waste as fertilizer to barley.

    Science.gov (United States)

    Haraldsen, Trond Knapp; Andersen, Uno; Krogstad, Tore; Sørheim, Roald

    2011-12-01

    This study examined the efficiency of different organic waste materials as NPK fertilizer, in addition to the risk for leaching losses related to shower precipitation in the first part of the growing season. The experiment was tested in a pot trial on a sandy soil in a greenhouse. Six organic fertilizers were evaluated: liquid anaerobic digestate (LAD) sourced from separated household waste, nitrified liquid anaerobic digestate (NLAD) of the same origin as LAD, meat and bone meal (MBM), hydrolysed salmon protein (HSP), reactor-composted catering waste (CW) and cattle manure (CM). An unfertilized control, calcium nitrate (CN) and Fullgjødsel® 21-4-10 were used as reference fertilizers. At equal amounts of mineral nitrogen both LAD and Fullgjødsel® gave equal yield of barley in addition to equal uptake of N, P, and K in barley grain. NLAD gave significantly lower barley yield than the original LAD due to leaching of nitrate-N after a simulated surplus of precipitation (28 mm) at Zadoks 14. There was significantly increased leaching of nitrate N from the treatments receiving 160 kg N ha(-1) of CN and NLAD in comparison with all the other organic fertilizers. In this study LAD performed to the same degree as Fullgjødsel® NPK fertilizer and it was concluded that LAD can be recommended as fertilizer for cereals. Nitrification of the ammonium N in the digestate caused significantly increased nitrate leaching, and cannot be recommended.

  10. Combustible gas production (methane) and biodegradation of solid and liquid mixtures of meat industry wastes

    Energy Technology Data Exchange (ETDEWEB)

    Marcos, A.; Al-Kassir, A.; Cuadros, F.; Lopez-Rodriguez, F. [School of Engineering, University of Extremadura, Avda. De Elva, s/n, 06071, Badajoz (Spain); Mohamad, A.A. [Department of Mechanical and Manufacturing Engineering, University of Calgary, 2500 University Dr. N.W., Calgary, Alberta (Canada)

    2010-05-15

    This work is devoted to determine the optimal operational conditions on the methane production as well as on the biodegradation obtained from the anaerobic codigestion of solid (fat, intestines, rumen, bowels, whiskers, etc.) and liquid (blood, washing water, manure, etc.) wastes of meat industry, particularly the ones rising from the municipal slaughterhouse of Badajoz (Spain). The experiments were performed using a 2 l capacity discontinuous digester at 38 C. The loading rate were 0.5, 1, 2, 3, and 4.5 g COD for wastewater (washing water and blood; Mixture 1), and 0.5, 1, 2, 3, and 4 g COD for the co-digestion of a mixture of 97% liquid effluent and 3% solid wastes v/v (Mixture 2) which represents the annual mean composition of the waste generated by the slaughterhouse. The maximal biodegradation rates obtained were: Mixture 1, 56.9% for a COD load of 1 g; and Mixture 2, 19.1% for a COD load of 2 g. For both mixtures, the greatest methane production was for the maximum COD load (4.5 g for Mixture 1, and 4 g for Mixture 2), at which values the amounts of methane obtained during and at the end of the co-digestion were practically indistinguishable between the two mixtures. The results will be used to design, construct, and establish the optimal operating conditions of a continuous complete-mixture biodigester. (author)

  11. Environmental assessment for liquid waste treatment at the Nevada Test Site, Nye County, Nevada

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-01-01

    This environmental assessment (EA) examines the potential impacts to the environment from treatment of low-level radioactive liquid and low-level mixed liquid and semi-solid wastes generated at the Nevada Test Site (NTS). The potential impacts of the proposed action and alternative actions are discussed herein in accordance with the National Environmental Policy Act (NEPA) of 1969, as amended in Title 42 U.S.C. (4321), and the US Department of Energy (DOE) policies and procedures set forth in Title 10 Code of Federal Regulations (CFR) Part 1021 and DOE Order 451.1, ``NEPA Compliance Program.`` The potential environmental impacts of the proposed action, construction and operation of a centralized liquid waste treatment facility, were addressed in the Final Environmental Impact Statement for the Nevada Test Site and Off-Site Locations in the State of Nevada. However, DOE is reevaluating the need for a centralized facility and is considering other alternative treatment options. This EA retains a centralized treatment facility as the proposed action but also considers other feasible alternatives.

  12. Imaging the oxidation effects of the Fenton reaction on phospholipids at the interface between aqueous phase and thermotropic liquid crystals.

    Science.gov (United States)

    Zhang, Minmin; Jang, Chang-Hyun

    2015-08-01

    The lipid peroxidation process has attracted much attention because of the growing evidence of its involvement in the pathogenesis of age-related diseases. Herein, we report a simple, label-free method to study the oxidation of phospholipids by the Fenton reaction at the interface between an aqueous phase and immiscible liquid crystals (LCs). The different images produced by the orientation of 4-cyano-4'-pentylbiphenyl (5CB) corresponded to the presence or absence of oxidized 1,2-dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt (DOPG). The oxidation effects of the Fenton reaction on DOPG were evaluated by monitoring the orientational response of liquid crystals upon contact with the oxidized DOPG solutions. DOPG was oxidized into chain-changed products containing hydroxy, carbonyl, or aldehyde groups, resulting in the rearrangement of the phospholipid layer. This induced the orientational transition of LCs from homeotropic to planar states; therefore, a dark to bright optical shift was observed. This shift was due to the Fenton reaction preventing DOPG to induce the orientational alignment of LCs at the aqueous/LC interface. We also used an ultraviolet spectrophotometer to confirm the effects of oxidation on phospholipids by the Fenton reaction. Using this simple method, a new approach for investigating phospholipid oxidation was established with high resolution and easy accessibility.

  13. Formation and characteristics of aqueous two-phase systems formed by a cationic surfactant and a series of ionic liquids.

    Science.gov (United States)

    Wei, Xi-Lian; Wang, Xiu-Hong; Ping, A-Li; Du, Pan-Pan; Sun, De-Zhi; Zhang, Qing-Fu; Liu, Jie

    2013-11-15

    Aqueous two-phase systems (ATPS) were obtained in the aqueous mixtures of a cationic surfactant and a series of ionic liquids (ILs). The effects of IL structure, temperature and additives on the phase separation were systematically investigated. The microstructures of some ATPS were observed by freeze-fracture replication technique. Lyotropic liquid crystal was found in the bottom phase besides micelles under different conditions. Remarkably, both IL structure and additives profoundly affected the formation and properties of the ATPSs. The phase separation can be attributed to the existence of different aggregates and the cation-π interactions of the cationic surfactant with the ILs, which has a significant role in the formation of ATPS. The extraction capacity of the studied ATPS was also evaluated through their application in the extraction of two biosubstances. The results indicate that the ILs with BF4(-) as anion show much better extraction efficiencies than the corresponding ILs with Br(-) as anion do under the same conditions. l-Tryptophan was mainly distributed into the NPTAB-rich phase, while methylene blue and capsochrome were mainly in the IL-rich phase.

  14. Thermodynamic study of the adsorption of chromium ions from aqueous solution on waste corn cobs material

    Directory of Open Access Journals (Sweden)

    Rafael A. Fonseca-Correa

    2014-12-01

    Full Text Available The paper shows the results of a study obtaining activated carbon from corn cobs and determining its use as an adsorbent for the removal of Cr3+ from aqueous solutions. The finely ground precursor was subjected to pyrolysis at 600 and 900 °C in a nitrogen atmosphere and chemical activation with H2O2 and HNO3. The effects of pyrolysis conditions and activation method on the physicochemical properties of the materials obtained were tested. The samples were characterised chemically and texturally. Were obtained microporous activated carbons of well-developed surface area varying from 337 to 1213 m2/g and exhibited differences acid-base character of the surface. The results obtained shows that a suitable good option of the activation procedure for corncobs permits the production of economic adsorbents with high sorption capacity for Cr3+ from aqueous solutions. A detailed study of immersion calorimetry was performed with carbons prepared from corn cobs to establish possible relationships with these materials between the enthalpies of immersion and textural and chemical parameters.

  15. Microbiology of formation waters from the deep repository of liquid radioactive wastes Severnyi.

    Science.gov (United States)

    Nazina, Tamara N; Kosareva, Inessa M; Petrunyaka, Vladimir V; Savushkina, Margarita K; Kudriavtsev, Evgeniy G; Lebedev, Valeriy A; Ahunov, Viktor D; Revenko, Yuriy A; Khafizov, Robert R; Osipov, George A; Belyaev, Sergey S; Ivanov, Mikhail V

    2004-07-01

    The presence, diversity, and geochemical activity of microorganisms in the Severnyi repository of liquid radioactive wastes were studied. Cultivable anaerobic denitrifiers, fermenters, sulfate-reducers, and methanogens were found in water samples from a depth of 162-405 m below sea level. Subsurface microorganisms produced methane from [2-(14)C]acetate and [(14)C]CO(2), formed hydrogen sulfide from Na(2) (35)SO(4), and reduced nitrate to dinitrogen in medium with acetate. The cell numbers of all studied groups of microorganisms and rates of anaerobic processes were higher in the zone of dispersion of radioactive wastes. Microbial communities present in the repository were able to utilise a wide range of organic and inorganic compounds and components of waste (acetate, nitrate, and sulfate) both aerobically and anaerobically. Bacterial production of gases may result in a local increase of the pressure in the repository and consequent discharge of wastes onto the surface. Microorganisms can indirectly decrease the mobility of radionuclides due to consumption of oxygen and production of sulfide, which favours deposition of metals. These results show the necessity of long-term microbiological and radiochemical monitoring of the repository.

  16. Development of a robust ionic liquid-based dispersive liquid-liquid microextraction against high concentration of salt for preconcentration of trace metals in saline aqueous samples: Application to the determination of Pb and Cd

    Energy Technology Data Exchange (ETDEWEB)

    Yousefi, Seyed Reza [School of Chemistry, University College of Science, University of Tehran, Tehran (Iran, Islamic Republic of); Shemirani, Farzaneh, E-mail: shemiran@khayam.ut.ac.ir [School of Chemistry, University College of Science, University of Tehran, Tehran (Iran, Islamic Republic of)

    2010-06-11

    A new ionic liquid-based dispersive liquid-liquid microextraction method was developed for preconcentration and determination of compounds in aqueous samples containing very high salt concentrations. This method can solve the problems associated with the limited application of the conventional IL-based DLLME in these samples. This is believed to arise from dissolving of the ionic liquids in aqueous samples with high salt content. In this method, the robustness of microextraction system against high salt concentration (up to 40%, w/v) is increased by introducing a common ion of the ionic liquid into the sample solution. The proposed method was applied satisfactorily to the preconcentration of lead and cadmium in saline samples. After preconcentration, the settled IL-phase was dissolved in 100 {mu}L ethanol and aspirated into the flame atomic absorption spectrometer (FAAS) using a home-made microsample introduction system. Several variables affecting the microextraction efficiency were investigated and optimized. Under the optimized conditions and preconcentration of only 10 mL of sample, the enhancement factors of 273 and 311 and the detection limits of 0.6 {mu}g L{sup -1} and 0.03 {mu}g L{sup -1} were obtained for lead and cadmium, respectively. Validation of the method was performed by both an analysis of a certified reference material (CRM) and comparison of results with those obtained by ISO standard method.

  17. Fluorescent derivatization combined with aqueous solvent-based dispersive liquid-liquid microextraction for determination of butyrobetaine, l-carnitine and acetyl-l-carnitine in human plasma.

    Science.gov (United States)

    Chen, Yi-Ching; Tsai, Chia-Ju; Feng, Chia-Hsien

    2016-09-16

    A novel aqueous solvent-based dispersive liquid-liquid microextraction (AS-DLLME) method was combined with narrow-bore liquid chromatography and fluorescence detection for the determination of hydrophilic compounds. A remover (non-polar solvent) and extractant (aqueous solution) were introduced into the derivatization system (acetonitrile) to obtain a water-in-oil emulsion state that increased the mass transfer of analytes. As a proof of concept, three quaternary ammonium substances, including butyrobetaine, l-carnitine and acetyl-l-carnitine, were also used as analytes and determined in pharmaceuticals, personal care products, food and human plasma. The analytes were derivatized with 4-bromomethylbiphenyl for fluorescence detection and improved retention in the column. The linear response was 10-2000nM for l-carnitine and acetyl-l-carnitine with a good determination coefficient (r(2)>0.998) in the standard solution. The detection limit for l-carnitine and acetyl-l-carnitine was 4.5 fmol. The method was also successfully applied to a 1μL sample of human plasma. In the linearity calculations for determining butyrobetaine, l-carnitine and acetyl-l-carnitine in human plasma, the determination coefficients ranged from 0.996 to 0.999. Linear regression exhibited good reproducibility and a relative standard deviation better than 7.50% for the slope and 9.06% for the intercept. To characterize highly hydrophilic compounds in various samples, the proposed method provides good sensitivity for a small sample volume with a low consumption of toxic solvents.

  18. Subsurface disposal of liquid low-level radioactive wastes at Oak Ridge, Tennessee

    Energy Technology Data Exchange (ETDEWEB)

    Stow, S.H.; Haase, C.S.

    1986-01-01

    At Oak Ridge National Laboratory (ORNL) subsurface injection has been used to dispose of low-level liquid nuclear waste for the last two decades. The process consists of mixing liquid waste with cement and other additives to form a slurry that is injected under pressure through a cased well into a low-permeability shale at a depth of 300 m (1000 ft). The slurry spreads from the injection well along bedding plane fractures and forms solid grout sheets of up to 200 m (660 ft) in radius. Using this process, ORNL has disposed of over 1.5 x 10/sup 6/ Ci of activity; the principal nuclides are /sup 90/Sr and /sup 137/Cs. In 1982, a new injection facility was put into operation. Each injection, which lasts some two days, results in the emplacement of approximately 750,000 l (180,000 gal) of slurry. Disposal cost per liter is approximately $0.30, including capital costs of the facility. This subsurface disposal process is fundamentally different from other operations. Wastes are injected into a low-permeability aquitard, and the process is designed to isolate nuclides, preventing dispersion in groundwaters. The porosity into which wastes are injected is created by hydraulically fracturing the host formation along bedding planes. The site is in the structurally complex Valley and Ridge Province. The stratigraphy consists of lower Paleozoic rocks. Investigations are under way to determine the long-term hydrologic isolation of the injection zone and the geochemical impact of saline groundwater on nuclide mobility. Injections are monitored by gamma-ray logging of cased observation wells to determine grout sheet orientation after an injection. Recent monitoring work has involved the use of tiltmeters, surface uplift surveys, and seismic arrays. 26 refs., 7 figs.

  19. A rotating disk apparatus for assessing the biodegradation of polycyclic aromatic hydrocarbons transferring from a non-aqueous phase liquid to solutions of surfactant Brij 35

    OpenAIRE

    Bernardez, Letícia Alonso

    2009-01-01

    Texto completo: acesso restrito. p. 415-424 A rotating disk apparatus was used to investigate the biodegradation of PAHs from non-aqueous phase liquids to solutions of Brij 35. The mass transfer of PAHs in absence of surfactant solution was not large enough to replenish the degraded PAHs. The addition of surfactant resulted in an overall enhancement of biodegradation rates compared to that observed in pure aqueous solution. This is because surfactant partition significant amount of PAHs in...

  20. Metal separations using aqueous biphasic partitioning systems

    Energy Technology Data Exchange (ETDEWEB)

    Chaiko, D.J.; Zaslavsky, B.; Rollins, A.N.; Vojta, Y.; Gartelmann, J.; Mego, W. [Argonne National Lab., IL (United States). Chemical Technology Div.

    1996-05-01

    Aqueous biphasic extraction (ABE) processes offer the potential for low-cost, highly selective separations. This countercurrent extraction technique involves selective partitioning of either dissolved solutes or ultrafine particulates between two immiscible aqueous phases. The extraction systems that the authors have studied are generated by combining an aqueous salt solution with an aqueous polymer solution. They have examined a wide range of applications for ABE, including the treatment of solid and liquid nuclear wastes, decontamination of soils, and processing of mineral ores. They have also conducted fundamental studies of solution microstructure using small angle neutron scattering (SANS). In this report they review the physicochemical fundamentals of aqueous biphase formation and discuss the development and scaleup of ABE processes for environmental remediation.

  1. Using oxidized liquid and solid human waste as nutrients for Chlorella vulgaris and cyanobacterium Oscillatoria deflexa

    Science.gov (United States)

    Trifonov, Sergey V.; Kalacheva, Galina; Tirranen, Lyalya; Gribovskaya, Iliada

    At stationary terrestrial and space stations with closed and partially closed substance exchange not only plants, but also algae can regenerate atmosphere. Their biomass can be used for feeding Daphnia and Moina species, which, in their turn, serve as food for fish. In addition, it is possible to use algae for production of biological fuel. We suggested two methods of human waste mineralization: dry (evaporation with subsequent incineration in a muffle furnace) and wet (oxidation in a reactor using hydrogen peroxide). The research task was to prepare nutrient media for green alga Chlorella vulgaris and cyanobacterium Oscillatoria deflexa using liquid human waste mineralized by dry method, and to prepare media for chlorella on the basis of 1) liquid and 2) liquid and solid human waste mineralized by wet method. The algae were grown in batch culture in a climate chamber with the following parameters: illumination 7 klx, temperature 27-30 (°) C, culture density 1-2 g/l of dry weight. The control for chlorella was Tamiya medium, pH-5, and for oscillstoria — Zarrouk medium, pH-10. Maximum permissible concentrations of NaCl, Cl, urea (NH _{2}) _{2}CO, and native urine were established for algae. Missing ingredients (such as salts and acids) for experimental nutrient media were determined: their addition made it possible to obtain the biomass production not less than that in the control. The estimation was given of the mineral and biochemical composition of algae grown on experimental media. Microbiological test revealed absence of foreign microbial flora in experimental cultures.

  2. Process for converting sodium nitrate-containing, caustic liquid radioactive wastes to solid insoluble products

    Science.gov (United States)

    Barney, Gary S.; Brownell, Lloyd E.

    1977-01-01

    A method for converting sodium nitrate-containing, caustic, radioactive wastes to a solid, relatively insoluble, thermally stable form is provided and comprises the steps of reacting powdered aluminum silicate clay, e.g., kaolin, bentonite, dickite, halloysite, pyrophyllite, etc., with the sodium nitrate-containing radioactive wastes which have a caustic concentration of about 3 to 7 M at a temperature of 30.degree. C to 100.degree. C to thereby entrap the dissolved radioactive salts in the aluminosilicate matrix. In one embodiment the sodium nitrate-containing, caustic, radioactive liquid waste, such as neutralized Purex-type waste, or salts or oxide produced by evaporation or calcination of these liquid wastes (e.g., anhydrous salt cake) is converted at a temperature within the range of 30.degree. C to 100.degree. C to the solid mineral form-cancrinite having an approximate chemical formula 2(NaAlSiO.sub.4) .sup.. xSalt.sup.. y H.sub.2 O with x = 0.52 and y = 0.68 when the entrapped salt is NaNO.sub.3. In another embodiment the sodium nitrate-containing, caustic, radioactive liquid is reacted with the powdered aluminum silicate clay at a temperature within the range of 30.degree. C to 100.degree. C, the resulting reaction product is air dried eitheras loose powder or molded shapes (e.g., bricks) and then fired at a temperature of at least 600.degree. C to form the solid mineral form-nepheline which has the approximate chemical formula of NaAlSiO.sub.4. The leach rate of the entrapped radioactive salts with distilled water is reduced essentially to that of the aluminosilicate lattice which is very low, e.g., in the range of 10.sup.-.sup.2 to 10.sup.-.sup.4 g/cm.sup.2 -- day for cancrinite and 10.sup.-.sup.3 to 10.sup.-.sup.5 g/cm.sup.2 -- day for nepheline.

  3. Adsorption of dissolved Reactive red dye from aqueous phase onto activated carbon prepared from agricultural waste.

    Science.gov (United States)

    Senthilkumaar, S; Kalaamani, P; Porkodi, K; Varadarajan, P R; Subburaam, C V

    2006-09-01

    The adsorption of Reactive red dye (RR) onto Coconut tree flower carbon (CFC) and Jute fibre carbon (JFC) from aqueous solution was investigated. Adsorption studies were carried out at different initial dye concentrations, initial solution pH and adsorbent doses. The kinetic studies were also conducted; the adsorption of Reactive red onto CFC and JFC followed pseudosecond-order rate equation. The effective diffusion coefficient was evaluated to establish the film diffusion mechanism. Quantitative removal of Reactive red dye was achieved at strongly acidic conditions for both the carbons studied. The adsorption isotherm data were fitted well to Langmuir isotherm and the adsorption capacity were found to be 181.9 and 200 mg/g for CFC and JFC, respectively. The overall rate of dye adsorption appeared to be controlled by chemisorption, in this case in accordance with poor desorption studies.

  4. Sorption of copper(II) from aqueous phase by waste biomass

    Energy Technology Data Exchange (ETDEWEB)

    Nagendra Rao, C.R. (Government Polytechnic, Anantapur (India)); Iyengar, L.; Venkobachar, C. (Indian Inst. of Tech., Kanpur (India))

    The objective of the present investigation is to compare three biomasses for copper uptake under different experimental conditions so as to choose the most suitable one for scaleup purposes. Ganoderma lucidum is a macrofungi, growing widely in tropical forests. Sorbent preparation requires its collection from the field. Asperigillus niger is obtained as a waste biomass from the fermentation industry. Activated sludge biomass is available from the biological waste treatment plants. The results of their potential to remove copper are presented. The copper uptake by biosorbents though, varied significantly, showed an increased trend in the range of pH 4 to 6. The increase in metal binding after alkali treatment was marginal for G. lucidum, significant for A. niger, and dramatic for sludge. Copper sorption capacities of M and M[sub c] were much higher than for other sorbents at pH 5.0. The effect of anionic ligands, like acetate and tartrate on copper uptake by raw and alkali treated biosorbents, was negligible as the predominant species in the presence of these ligands is divalent copper ion. Pyrophosphate, citrate, and EDTA had varying degrees of adverse effects on metal uptake. Thus, among the sorbents G. lucidum in its raw form is best suited for the practical application of copper removal from industrial effluents.

  5. Efficient photochemical decomposition of long-chain perfluorocarboxylic acids by means of an aqueous/liquid CO2 biphasic system.

    Science.gov (United States)

    Hori, Hisao; Yamamoto, Ari; Kutsuna, Shuzo

    2005-10-01

    Photochemical decomposition of persistent and bioaccumulative long-chain (C9-C11) perfluorocarboxylic acids (PFCAs) with persulfate ion (S2O8(2-)) in an aqueous/liquid CO2 biphasic system was examined to develop a technique to neutralize stationary sources of the long-chain PFCAs. The long-chain PFCAs, namely, perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), and perfluoroundecanoic acid (PFUA), which are used as emulsifying agents and as surface treatment agents in industry, are relatively insoluble in water but are soluble in liquid CO2; therefore, introduction of liquid CO2 to the aqueous photoreaction system reduces the interference of colloidal PFCA particles. When the biphasic system was used to decompose these PFCAs, the extent of reaction was 6.4-51 times as high as that achieved in the absence of CO2. In the biphasic system, PFNA, PFDA, and PFUA (33.5-33.6 micromol) in 25.0 mL of water were 100%, 100%, and 77.1% decomposed, respectively, after 12 h of irradiation with a 200-W xenon-mercury lamp; F- ions were produced as a major product, and short-chain PFCAs, which are less bioaccumulative than the original PFCAs, were minor products. All of the initial S2O8(2-) was transformed to SO42-. The system also efficiently decomposed PFCAs at lower concentrations (e.g., 4.28-16.7 micromol of PFDA in 25.0 mL) and was successfully applied to decompose PFNA in floor wax.

  6. The development of a cholesterol biosensor using a liquid crystal/aqueous interface in a SDS-included β-cyclodextrin aqueous solution.

    Science.gov (United States)

    Munir, Sundas; Park, Soo-Young

    2015-09-17

    Sodium dodecyl sulphate (SDS) including β-cyclodextrin (β-CD) (β-CDSDS) was used to detect cholesterol at the 4-cyano-4'-pentylbiphenyl (5CB)/aqueous interface in transmission electron microscopy (TEM) grid cells. The β-CD acts as a host for SDS (guest). The guest SDS enclosed within the β-CD cavity was replaced with cholesterol by injecting cholesterol solution into the TEM cell at concentrations greater than 3 μM. The replacement of SDS with cholesterol was confirmed by pH measurement and high performance liquid chromatography (HPLC). The SDS excluded from the β-CD altered the planar orientation of the 5CB confined within the TEM grid cell to a homeotropic orientation. This planar-to-homeotropic transition was observed using a polarized optical microscope under crossed polarizers. This convenient TEM grid cell provides a new method for the selective detection of cholesterol without immobilization of the detecting receptors (enzyme, antibody, or aptamer) or the use of sophisticated instruments.

  7. Prediction of liquid-liquid equilibria for polyethylene glycol based aqueous two-phase system by ASOG and UNIFAC method

    Directory of Open Access Journals (Sweden)

    M. Perumalsamy

    2009-03-01

    Full Text Available Liquid-Liquid equilibrium data were obtained for the polyethylene glycol2000(PEG2000-sodium citrate-water system at 298.15, 308.15 and 318.15 K. The effect of temperature on binodal and tie line data was studied and published in a previous article (Murugesan and Perumalsamy, 2005. The interaction parameters of ASOG and UNIFAC models were estimated using the LLE data of PEG2000-sodium citrate-water system and are used to predict the LLE data for PEG6000-sodium citrate-water system at 298.15, 308.15 and 318.15 K (literature data. The predicted LLE data by both ASOG and UNIFAC models showed good agreement with the experimental and literature data.

  8. Use of textile waste water along with liquid NPK fertilizer for production of wheat on saline sodic soils.

    Science.gov (United States)

    Yaseen, Muhammad; Aziz, Muhammad Zahir; Jafar, Abdul Aleem; Naveed, Muhammad; Saleem, Muhammad

    2016-01-01

    A field experiment in collaboration with a private textile industry (Noor Fatima Fabrics Private (Ltd.), Faisalabad) was conducted to evaluate the effect of disposed water from bleaching unit, printing unit and end drain for improving growth and yield of wheat under saline sodic soil. Textile waste water along with canal water (control) was applied with and without liquid NPK fertilizer. The application of liquid NPK fertilizer with end drain waste water increased plant height, spike length, flag leaf length, root length, number of tillers (m(-2)), number of fertile tillers (m(-2)), 1000 grain weight, grain yield, straw yield and biological yield up to 21, 20, 20, 44, 17, 20, 14, 44, 40 and 41%, respectively compared to canal water (control). Similarly, the NPK uptake in grain was increased up to 15, 30 and 28%, respectively by liquid fertilizer treated end drain water as compare to canal water with liquid fertilizer. Moreover, concentration of different heavy metals particularly Cu, Cr, Pb and Cd was decreased in grains by application of waste water along with liquid NPK. The result may imply that waste water application along with liquid-NPK could be a novel approach for improving growth and yield of wheat in saline sodic soils.

  9. Efficiency Study of Nickel (II and Cadmium (II Biosorption by Powder of Waste Activated Sludge from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    A.A Ebrahimi

    2011-01-01

    Full Text Available "n "n "nBackground and Objective: Nickel (II and cadmium (II are important in environmental pollutant. Biosorption of heavy metals can be an effective process for the removal and recovery of heavy metal ions from aqueous solutions because of the decrease in sludge problems, economical issues, high efficiency and compatibility with the environment."nMaterials and Methods: power of wasted activated sludge have been contact with nickel (II and cadmium (II solutions in 0.25 and 0.75 milli molar invarious pHs and mixing pace, at 24-26 0C temperature on batch reactor system .After two hours (continuously 5-420 min in kinetic study samples were analyzed with atomic absorption spectrophotometer."nResults:The kinetic study results show that equilibrium adsorption time for nickel (II and cadmium"n(II reached within 2 hr, but the profile curve of cadmium (II biosorption was smoother than nickel (II biosorption. Both metals adsorption followed the Langmuir model and the maximum adsorption capacity (qmax for nickel (II and cadmium (II was 0.195 and 0.37 milli mole per gram respectively. The increase in pH resulted in adsorption increase for both metals. For cadmium (II at 0.25 and 0.75 mMinitial concentration there was no adsorption at pH 2 where as nickel (0.25 mM adsorption was observed at the same pH. The optimum mixing rate for both metals was 200 rpm and this effect was more obviously in greater concentration."nConclusion: Like othe biosorbents ,wasted activated sludge showed greater capacity for cadmium(II biosorption than nickel (II. Cadmium (II in modeling and biosorption characteristics study had more conformity than nickel (II.

  10. Hyperbranched polyglycerol/graphene oxide nanocomposite reinforced hollow fiber solid/liquid phase microextraction for measurement of ibuprofen and naproxen in hair and waste water samples.

    Science.gov (United States)

    Rezaeifar, Zohreh; Es'haghi, Zarrin; Rounaghi, Gholam Hossein; Chamsaz, Mahmoud

    2016-09-01

    A new design of hyperbranched polyglycerol/graphene oxide nanocomposite reinforced hollow fiber solid/liquid phase microextraction (HBP/GO -HF-SLPME) coupled with high performance liquid chromatography used for extraction and determination of ibuprofen and naproxen in hair and waste water samples. The graphene oxide first synthesized from graphite powders by using modified Hummers approach. The surface of graphene oxide was modified using hyperbranched polyglycerol, through direct polycondensation with thionyl chloride. The ready nanocomposite later wetted by a few microliter of an organic solvent (1-octanol), and then applied to extract the target analytes in direct immersion sampling mode.After the extraction process, the analytes were desorbed with methanol, and then detected via high performance liquid chromatography (HPLC). The experimental setup is very simple and highly affordable. The main factors influencing extraction such as; feed pH, extraction time, aqueous feed volume, agitation speed, the amount of functionalized graphene oxide and the desorption conditions have been examined in detail. Under the optimized experimental conditions, linearity was observed in the range of 5-30,000ngmL(-1) for ibuprofen and 2-10,000ngmL(-1) for naproxen with correlation coefficients of 0.9968 and 0.9925, respectively. The limits of detection were 2.95ngmL(-1) for ibuprofen and 1.51ngmL(-1) for naproxen. The relative standard deviations (RSDs) were found to be less than 5% (n=5).

  11. Degradation Product Partitioning in Source Zones Containing Chlorinated Ethene Dense Non-Aqueous-Phase Liquid

    Science.gov (United States)

    2010-01-01

    xx, XXXX / ENVIRONMENTAL SCIENCE & TECHNOLOGY 9 A Report Documentation Page Form ApprovedOMB No. 0704-0188 Public reporting burden for the...exp(viL(P - Pref)RT ) (4) B 9 ENVIRONMENTAL SCIENCE & TECHNOLOGY / VOL. , NO. xx, XXXX systems of m components the Henry law coefficient for... ENVIRONMENTAL SCIENCE & TECHNOLOGY 9 C cis-DCE had a negligible influence on the molar volume of the aqueous solution. The solubility of VC was

  12. Potential Malaysia agricultural waste materials for the biosorption of cadmium(II) from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Foo, L.P.Y.; Tee, C.Z.; Raimy, N.R.; Hassell, D.G.; Lee, L.Y. [University of Nottingham Malaysia Campus, Semenyih, Selangor (Malaysia)

    2012-04-15

    Biosorption of cadmium(II) ions (Cd{sup 2+}) onto Ananas comosus (AC) peel, Parkia speciosa (PS) pods and Psidium guajava (PG) peel were investigated in this study. Batch sorption experiments were performed by investigating the effect of initial pH. It was found that Cd{sup 2+} uptake was highly dependent on the initial pH and Cd{sup 2+} removal efficiency was highest for PG peel, followed by AC peel and PS pods. Biosorption experiments were carried out using different initial Cd{sup 2+} concentration and the experimental data obtained was fitted to both Langmuir and Freundlich isotherms. The experimental data was found to best fit the Langmuir isotherm, and adsorption capacities of 18.21 mg/g (AC peel), 25.64 mg/g (PS pods) and 39.68 mg/g (PG peel) were obtained. Comparison with published adsorption capacities for other low-cost biosorbents indicates that PS pods and PG peel have potential as low-cost biosorbent materials for the removal of Cd{sup 2+} from aqueous solution. (orig.)

  13. Uncoupling of liquid and solid retention times in anaerobic digestion of catering wastes.

    Science.gov (United States)

    Climenhaga, M A; Banks, C J

    2008-01-01

    Source-separated food wastes collected from a university campus catering facility were processed in bench-scale anaerobic digesters. The feedstock contained a varied mix of fruits, vegetables, meats and fried foods. Two modes of digestion were compared. The first was hydraulic flush (HF) mode, in which liquids were flushed through the reactor on a retention time of 25 days while solids were maintained on an extended retention time of over 150 days. The converse was a solids wastage (SW) mode, in which liquid retention time was over 150 days, and solids were wasted to maintain a retention time of 25 days. SW reactors exhibited methanogenic failure after approximately 45 days. HF reactors, in contrast, maintained stable digestion for a period of 100 days, and were robust enough to recover from a thermal shock applied over a three-day period in which the temperature was increased from 35 degrees C to 50 degrees C between days 105-108 of the experiment. Stable operation was regained by day 139 and continued until the end of the run on day 150.

  14. Hauled liquid waste as a pollutant of soils and waters in Poland

    Directory of Open Access Journals (Sweden)

    Karczmarczyk Agnieszka

    2016-06-01

    Full Text Available Hauled liquid waste as a pollutant of soils and waters in Poland. Improperly maintained holding tanks are often underestimated source of contamination of soil, groundwater and surface water. As a rule, wastewater stored in holding tanks, should be transported and treated in municipal wastewater treatment plants (WWTPs. There are 2,257,000 holding tanks in Poland, located mainly in rural areas. The article presents the results of analysis of wastewater management in 20 rural and urban-rural communes, which were chosen at random from the total number of 2,174 communes in Poland. The only criterion of commune selection was total or partial lack of sewerage system. Analysis of the collected data showed that on average only 27% of liquid waste from holding tanks ended at the WWTPs. The median is even lower and amounts to 17.5%. More than 4,000 Mg of P and 26,000 Mg of N is dispersed in the environment in uncontrolled manner. Those diffuse point sources of pollution may be one of the reasons in the difficulty of achieving of good ecological status of rivers and affect the quality of the Baltic Sea.

  15. Acid Separation, Catalytic Oxidation and Coagulation for ATC Waste Liquid Treatment

    Institute of Scientific and Technical Information of China (English)

    DING Xiaoling; JIA Chunning

    2005-01-01

    It is difficult to treat 2-amino-thiazoline-4-carboxylic acid (ATC) waste liquid effectively at present for its characteristics of high chemical oxygen demand (COD), high salinity and low biodegradability. In order to solve this problem, this paper presents several kinds of physical-chemical treatment unit techniques, including acid separation, catalytic oxidation and coagulation. First of all, acid separation was adopted to precipitate relevant organics at isoelectric point. When the temperature and pH value of acid separation were controlled at about 5 ℃ and 2.2 respectively, the COD removal rate could reach 27.6%. Secondly, oxidation was used to break chemical constitution of refractory organics. The optimal reaction parameters of catalytic oxidation should be 20 ℃, pH adjusted to 5.0 and [Fe2+] 300 mg/L. Then with 5% H 2O 2 added and after one-hour reaction, the COD removal rate could achieve about 52%. Finally, coagulation was adopted to remove a portion of refractory organics, and 15% polymeric molysite flocculant was the best for the coagulation, and the COD removal rate could reach about 15%. Therefore, the proposed feasible process of physical-chemical pretreatment for ATC waste liquid could have about 70% COD removed in total.

  16. Nuclide separation modeling through reverse osmosis membranes in radioactive liquid waste

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Byung Sik [KEPCO Engineering and Construction, Gimcheon (Korea, Republic of)

    2015-12-15

    The aim of this work is to investigate the transport mechanism of radioactive nuclides through the reverse osmosis (RO) membrane and to estimate its effectiveness for nuclide separation from radioactive liquid waste. An analytical model is developed to simulate the RO separation, and a series of experiments are set up to confirm its estimated separation behavior. The model is based on the extended Nernst-Plank equation, which handles the convective flux, diffusive flux, and electromigration flux under electroneutrality and zero electric current conditions. The distribution coefficient which arises due to ion interactions with the membrane material and the electric potential jump at the membrane interface are included as boundary conditions in solving the equation. A high Peclet approximation is adopted to simplify the calculation, but the effect of concentration polarization is included for a more accurate prediction of separation. Cobalt and cesium are specifically selected for the experiments in order to check the separation mechanism from liquid waste composed of various radioactive nuclides and nonradioactive substances, and the results are compared with the estimated cobalt and cesium rejections of the RO membrane using the model. Experimental and calculated results are shown to be in excellent agreement. The proposed model will be very useful for the prediction of separation behavior of various radioactive nuclides by the RO membrane.

  17. Pyrolysis characteristics and pyrolysis products separation for recycling organic materials from waste liquid crystal display panels.

    Science.gov (United States)

    Wang, Ruixue; Xu, Zhenming

    2016-01-25

    Waste liquid crystal display (LCD) panels mainly contain inorganic materials (glass substrate with indium-tin oxide film), and organic materials (polarizing film and liquid crystal). The organic materials should be removed beforehand since the organic matters would hinder the indium recycling process. In the present study, pyrolysis process is used to remove the organic materials and recycle acetic as well as and triphenyl phosphate (TPP) from waste LCD panels in an environmental friendly way. Several highlights of this study are summarized as follows: (i) Pyrolysis characteristics and pyrolysis kinetics analysis are conducted which is significant to get a better understanding of the pyrolysis process. (ii) Optimum design is developed by applying Box-Behnken Design (BBD) under response surface methodology (RSM) for engineering application which is significant to guide the further industrial recycling process. The oil yield could reach 70.53 wt% and the residue rate could reach 14.05 wt% when the pyrolysis temperature is 570 °C, nitrogen flow rate is 6 L min(-1) and the particle size is 0.5 mm. (iii) Furthermore, acetic acid and TPP are recycled, and then separated by rotary evaporation, which could reduce the consumption of fossil energy for producing acetic acid, and be reused in electronics manufacturing industry.

  18. Design and development of single stage purification of papain using Ionic Liquid based aqueous two phase extraction system and its Partition coefficient studies

    Directory of Open Access Journals (Sweden)

    Senthilkumar Rathnasamy

    2013-04-01

    Full Text Available As an emerging trend in bioseparation, aqueous two phase extractions based on phosponium ionic liquid have been utilized in this work to extract papain from Carica papaya fruit latex and the same wascompared with conventional aqueous two phase extraction system. Factors affecting the partition coefficient of papain such as ionic liquid concentration, pH of the extraction system and temperature have been investigated. The optimization studies show that ionic liquid concentrations and pH are majorly influencing the phaseformations and papain partitioning. It reveals the importance of electrostatic and hydrophobic interactions in the papain partitioning. Purification studies performed on Gel Filtration Chromatography shows that 96% of the papain enzyme could be extracted with the phosponium based ionic liquid in a single stage extraction. The final fraction containing papain enzyme was confirmed by SDS Page analysis.

  19. Separation, concentration and determination of chloramphenicol in environment and food using an ionic liquid/salt aqueous two-phase flotation system coupled with high-performance liquid chromatography.

    Science.gov (United States)

    Han, Juan; Wang, Yun; Yu, Cuilan; Li, Chunxiang; Yan, Yongsheng; Liu, Yan; Wang, Liang

    2011-01-31

    Ionic liquid-salt aqueous two-phase flotation (ILATPF) is a novel, green, non-toxic and sensitive samples pretreatment technique. ILATPF coupled with high-performance liquid chromatography (HPLC) was developed for the analysis of chloramphenicol, which combines ionic liquid aqueous two-phase system (ILATPS) based on imidazolium ionic liquid (1-butyl-3-methylimidazolium chloride, [C(4)mim]Cl) and inorganic salt (K(2)HPO(4)) with solvent sublation. In ILATPF systems, phase behaviors of the ILATPF were studied for different types of ionic liquids and salts. The sublation efficiency of chloramphenicol in [C(4)mim]Cl-K(2)HPO(4) ILATPF was influenced by the types of salts, concentration of K(2)HPO(4) in aqueous solution, solution pH, nitrogen flow rate, sublation time and the amount of [C(4)mim]Cl. Under the optimum conditions, the average sublation efficiency is up to 98.5%. The mechanism of ILATPF contains two principal processes. One is the mechanism of IL-salt ILATPS formation, the other is solvent sublation. This method was practical when applied to the analysis of chloramphenicol in lake water, feed water, milk, and honey samples with the linear range of 0.5-500 ng mL(-1). The method yielded limit of detection (LOD) of 0.1 ng mL(-1) and limit of quantification (LOQ) of 0.3 ng mL(-1). The recovery of CAP was 97.1-101.9% from aqueous samples of environmental and food samples by the proposed method. Compared with liquid-liquid extraction, solvent sublation and ionic liquid aqueous two-phase extraction, ILATPF can not only separate and concentrate chloramphenicol with high sublation efficiency, but also efficiently reduce the wastage of IL. This novel technique is much simpler and more environmentally friendly and is suggested to have important applications for the concentration and separation of other small biomolecules.

  20. A Study of Investigation-Derived Waste Management Options

    Science.gov (United States)

    1993-09-01

    Chloroform 72 Nickel 72 Mercury 71 Vinyl Chloride 71 Acetone 67 Chromium (III) 66 Trichloroethane, 1,1,1- 65 In general, characteristics of IDW fall into...substances (e.g., container specimen waste, light or dense non-aqueous phase liquids [LNAPL, DNAPL ], etc.), the DRMO method may provide a feasible means of...Environmental Restoration Account DERP -- Defense Environmental Restoration Program DNAPL -- Dense Non-Aqueous Phase Liquids DOD -- Department of Defense

  1. Ultrasound-assisted dispersive liquid-liquid microextraction for the determination of synthetic musk fragrances in aqueous matrices by gas chromatography-mass spectrometry.

    Science.gov (United States)

    Homem, Vera; Alves, Alice; Alves, Arminda; Santos, Lúcia

    2016-01-01

    A rapid and simple method for the simultaneous determination of twelve synthetic musks in water samples, using ultrasound-assisted dispersive liquid-liquid microextraction (UA-DLLME) coupled with gas chromatography-mass spectrometry (GC-MS) was successfully developed. The influence of seven factors (volume of the extraction solvent and disperser solvent, sample volume, extraction time, ionic strength, type of extraction and disperser solvent) affecting the UA-DLLME extraction efficiency was investigated using a screening design. The significant factors were selected and optimised employing a central composite design: 80 μL of chloroform, 880 μL of acetonitrile, 6 mL of sample volume, 3.5% (wt) of NaCl and 2 min of extraction time. Under the optimised conditions, this methodology was successfully validated for the analysis of 12 synthetic musk compounds in different aqueous samples (tap, sea and river water, effluent and influent wastewater). The proposed method showed enrichment factors between 101 and 115 depending on the analyte, limits of detection in the range of 0.004-54 ng L(-1) and good repeatability (most relative standard deviation values below 10%). No significant matrix effects were found, since recoveries ranged between 71% and 118%. Finally, the method was satisfactorily applied to the analysis of five different aqueous samples. Results demonstrated the existence of a larger amount of synthetic musks in wastewaters than in other water samples (average concentrations of 2800 ng L(-1) in influent and 850 ng L(-1) in effluent). Galaxolide, tonalide and exaltolide were the compounds most detected.

  2. EXPLORING ENGINEERING CONTROL THROUGH PROCESS MANIPULATION OF RADIOACTIVE LIQUID WASTE TANK CHEMICAL CLEANING

    Energy Technology Data Exchange (ETDEWEB)

    Brown, A.

    2014-04-27

    One method of remediating legacy liquid radioactive waste produced during the cold war, is aggressive in-tank chemical cleaning. Chemical cleaning has successfully reduced the curie content of residual waste heels in large underground storage tanks; however this process generates significant chemical hazards. Mercury is often the bounding hazard due to its extensive use in the separations process that produced the waste. This paper explores how variations in controllable process factors, tank level and temperature, may be manipulated to reduce the hazard potential related to mercury vapor generation. When compared using a multivariate regression analysis, findings indicated that there was a significant relationship between both tank level (p value of 1.65x10{sup -23}) and temperature (p value of 6.39x10{sup -6}) to the mercury vapor concentration in the tank ventilation system. Tank temperature showed the most promise as a controllable parameter for future tank cleaning endeavors. Despite statistically significant relationships, there may not be confidence in the ability to control accident scenarios to below mercury’s IDLH or PAC-III levels for future cleaning initiatives.

  3. Development and testing of ion exchangers for treatment of liquid wastes at Oak Ridge National Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Collins, J.L.; Davidson, D.J.; Chase, C.W.; Egan, B.Z. (Oak Ridge National Lab., TN (United States)); Ensor, D.D.; Bright, R.M.; Glasgow, D.C. (Tennessee Technological Univ., Cookeville, TN (United States))

    1993-03-01

    This report addresses three areas of waste treatment: (1) treatment of newly generated low-level liquid waste and Melton Valley Storage Tank (MVST) supernate using inorganic ion exchangers; (2) treatment of processing streams at the Radiochemical Engineering Development Center (REDC); and (3) removal of radionuclides from organic solutions. Distribution of various radionuclides between simulated waste solutions and several sorbents was determined in batch tests. Inorganic ion exchangers were prepared in the form of microspheres by an intemal gelation process. Microspheres of hydrous titania, hydrous zirconia, hydrous titania containing embedded sodium cobalt hexacyanoferrate, and the corresponding phosphate forms of these materials were prepared. Several zeolites (PDZ-140, PDZ-300, EE-96, CBV-10A) and inorganic ion exchangers (hydrous titania, hydrous zirconia, polyantimanic acid, sodium cobalt hexacyanoferrate) were tested for the removal of cesium and strontium from the acidic simulated Cleanex raffinate generated at REDC. A resorcinol-based ion-exchange resin and three types of sodium titanate were tested for removal of cesium and strontium from the REDC caustic dissolver solution. Hydrous titania, hydrous zirconia, and their corresponding phosphates were tested for the removal of Eu[sup 3+] from various solutions of di-2-ethylbexyl phosphoric acid (HDEHP) in toluene or dodecane.

  4. Development and testing of ion exchangers for treatment of liquid wastes at Oak Ridge National Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Collins, J.L.; Davidson, D.J.; Chase, C.W.; Egan, B.Z. [Oak Ridge National Lab., TN (United States); Ensor, D.D.; Bright, R.M.; Glasgow, D.C. [Tennessee Technological Univ., Cookeville, TN (United States)

    1993-03-01

    This report addresses three areas of waste treatment: (1) treatment of newly generated low-level liquid waste and Melton Valley Storage Tank (MVST) supernate using inorganic ion exchangers; (2) treatment of processing streams at the Radiochemical Engineering Development Center (REDC); and (3) removal of radionuclides from organic solutions. Distribution of various radionuclides between simulated waste solutions and several sorbents was determined in batch tests. Inorganic ion exchangers were prepared in the form of microspheres by an intemal gelation process. Microspheres of hydrous titania, hydrous zirconia, hydrous titania containing embedded sodium cobalt hexacyanoferrate, and the corresponding phosphate forms of these materials were prepared. Several zeolites (PDZ-140, PDZ-300, EE-96, CBV-10A) and inorganic ion exchangers (hydrous titania, hydrous zirconia, polyantimanic acid, sodium cobalt hexacyanoferrate) were tested for the removal of cesium and strontium from the acidic simulated Cleanex raffinate generated at REDC. A resorcinol-based ion-exchange resin and three types of sodium titanate were tested for removal of cesium and strontium from the REDC caustic dissolver solution. Hydrous titania, hydrous zirconia, and their corresponding phosphates were tested for the removal of Eu{sup 3+} from various solutions of di-2-ethylbexyl phosphoric acid (HDEHP) in toluene or dodecane.

  5. Usefulness of ANN-based model for copper removal from aqueous solutions using agro industrial waste materials

    Directory of Open Access Journals (Sweden)

    Petrović Marija S.

    2015-01-01

    Full Text Available The purpose of this study was to investigate the adsorption properties of locally available lignocelluloses biomaterials as biosorbents for the removal of copper ions from aqueous solution. Materials are generated from juice production (apricot stones and from the corn milling process (corn cob. Such solid wastes have little or no economic value and very often present a disposal problem. Using batch adsorption techniques the effects of initial Cu(II ions concentration (Ci, amount of biomass (m and volume of metal solution (V, on biosorption efficiency and capacity were studied for both materials, without any pre-treatments. The optimal parameters for both biosorbents were selected depending on a highest sorption capability of biosorbent, in removal of Cu(II. Experimental data were compared with second order polynomial regression models (SOPs and artificial neural networks (ANNs. SOPs showed acceptable coefficients of determination (0.842 - 0.997, while ANNs performed high prediction accuracy (0.980-0.986 in comparison to experimental results. [Projekat Ministarstva nauke Republike Srbije, br. TR 31003, TR 31055

  6. The Predisposition of Iraqi Rice Husk to Remove Heavy Metals from Aqueous Solutions and Capitalized from Waste Residue

    Directory of Open Access Journals (Sweden)

    Mohammed Nsaif

    2013-12-01

    Full Text Available This study is deal with study the potential of Iraqi Rice Husk (IRH on the removal of three heavy metals pollutant which were (Mg, Mn and Mo ions from industrial wastewater using different design parameters by adsorption process. Results show that the removal efficiency were (93.95, 97.18 and 95.26 % for heavy metal (Mg, Mn and Mo respectively from aquatic solution decreased with increasing of initial concentration and flow rate while the removal efficiency increased with increasing absorbance material bed height, pH and feeding temperature. Statistical model is achieved to find an expression relates the overall operating parameters with the removal efficiency for each metal ions used in this investigation in a general equation (each one alone. The samples of (IRH remaining after using it in the removal of (Mg, Mn and Mo heavy metal ions above from Simulated Synthetic Aqueous Solutions (SSAS to investigate the capitalized of it in different methods. Different benefits possess which are: remove the three toxic heavy metals ions contaminated the water, get rid of agricultural waste (IRH, in the same time, produce light and more benefit hydrocarbons from n-heptane isomerization using a type Y-zeolite catalyst synthesis from remaining (IRH and prepare a cheap and active rodenticide.

  7. Uptake of Pb(II ion From Aqueous Solution Using Silk Cotton Hull Carbon: An Agricultural Waste Biomass

    Directory of Open Access Journals (Sweden)

    R. Shanmugavalli

    2006-01-01

    Full Text Available Activated carbon prepared from silk cotton hull (SCH was used for the adsorptive removal of Pb(II ion from aqueous solution. The raw material used for the preparation of activated carbon is the waste of agricultural product; the production of this carbon is expected to be economically feasible. Parameters such as agitation time, metal ion concentration, adsorbent dose, pH and Particle size were studied. Adsorption equilibrium was reached within 80 min for 10, 20, 30 and 40mg/l of Pb(II ion with 50mg of carbon per mL of solution. Adsorption parameters were determined using both Langmuir and Freundlich isotherm models. The adsorption efficiency reached 100% for 20, 30 and 40mg/l of Pb(II ion with 120, 140 and 150mg of carbon. Pb(II ion removal increased as the pH increased from 2 to 5 and remains constant up to pH 10. Desorption studies were also carried out with dilute hydrochloric acid to know the mechanism of adsorption. Quantitative desorption of Pb(II ion from carbon indicates that adsorption of metal ion is by ion-exchange. Efficiency of the adsorption of SCH was also studied with Pb containing industrial wastewater by varying pH and carbon concentration.

  8. Application of potato (Solanum tuberosum plant wastes for the removal of methylene blue and malachite green dye from aqueous solution

    Directory of Open Access Journals (Sweden)

    Neha Gupta

    2016-09-01

    Full Text Available Dye pollutants from the textile, paper, and leather industries are important sources of environmental contamination. In the present study an agricultural waste from potato plant (potato stem powder, PSP and potato leaves powder, PLP was used as an adsorbent for removal of the methylene blue (MB and malachite green (MG dyes from aqueous solution. The adsorbent materials were characterized by scanning electron microscope (SEM and Fourier transform infrared (FTIR spectroscopy. Batch experiments were performed to investigate the effect of physico-chemical parameters, such as pHpzc, ionic strength, adsorbent dose, contact time, initial dyes concentration and temperature. The kinetics of adsorption was studied by applying the pseudo-first order, pseudo-second order and intraparticle diffusion models. The pseudo-second order model better represented the adsorption kinetics and the mechanism was controlled by surface adsorption and intraparticle diffusion. Equilibrium data were analyzed using Langmuir and Freundlich isotherm models. The thermodynamic parameters such as change in enthalpy (ΔH°, entropy (ΔS° and Gibb’s free energy (ΔG° of adsorption systems were also determined and evaluated.

  9. Optimization of Aqueous Extraction Conditions for Recovery of Phenolic Content and Antioxidant Properties from Macadamia (Macadamia tetraphylla Skin Waste

    Directory of Open Access Journals (Sweden)

    Adriana Dailey

    2015-11-01

    Full Text Available The macadamia is native to Australia and is now grown commercially around the world. Macadamia skin, known as waste, has been generated abundantly, but this ample source has had limited uses as a byproduct. The aim of this study was to develop optimal aqueous extraction conditions for the recovery of phenolic compounds and antioxidant properties from macadamia skin using Response Surface Methodology (RSM. Water was selected for optimizing the extraction conditions because it is a cheap, safe, and environmentally friendly solvent. The results showed that the RSM models were reliable for the prediction and evaluation of the tested variables. Within the tested ranges, temperature (°C, time (min, and sample-to-solvent ratio (g/100 mL, and their interactions, did not significantly affect phenolic compound (TPC, flavonoid, proanthocyanidin, CUPRAC, and FRAP contents. However, the time and the sample-to-solvent ratio significantly affected DPPH antioxidant activity and the ratio significantly affected ABTS antioxidant capacity. The optimal extraction conditions for the recovery of phenolic compounds and antioxidant properties were predicted and validated at a temperature of 90 °C, a time of 20 min, and a sample-to-solvent ratio of 5 g/100 mL. At these conditions, an extract with TPC of 86 mg GAE/g, flavonoids of 30 mg RUE/g, and proanthocyanidins of 97 mg CAE/g could be prepared with potent antioxidant capacity.

  10. Research on the treatment of liquid waste containing cesium by an adsorption-microfiltration process with potassium zinc hexacyanoferrate

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Changping, E-mail: melindazhang@yahoo.com.cn [School of Environmental Science and Engineering, Tianjin University, Tianjin, 300072 (China); Gu Ping, E-mail: guping@tju.edu.cn [School of Environmental Science and Engineering, Tianjin University, Tianjin, 300072 (China); Zhao Jun; Zhang Dong; Deng Yue [Institute of Nuclear Physics and Chemistry, Chinese Academy of Engineering Physics, Mianyang 621900 (China)

    2009-08-15

    The removal of cesium from an aqueous solution by an adsorption-microfiltration (AMF) process was investigated in jar tests and lab-scale tests. The adsorbent was K{sub 2}Zn{sub 3}[Fe(CN){sub 6}]{sub 2}. The obtained cesium data in the jar test fit a Freundlich-type isotherm well. In the lab-scale test, the mean cesium concentration of the raw water and the effluent were 106.87 {mu}g/L and 0.59 {mu}g/L, respectively, the mean removal of cesium was 99.44%, and the mean decontamination factors (DF) and concentration factors (CF) were 208 and 539, respectively. The removal of cesium in the lab-scale test was better than that in the jar test because the old adsorbents remaining in the reactor still had adsorption capacity with the premise of no significant desorption being observed, and the continuous renewal of the adsorbent surface improved the adsorption capacity of the adsorbent. Some of the suspended solids were deposited on the bottom of the reactor, which would affect the mixing of adsorbents with the raw water and the renewing of the adsorbent surface. Membrane fouling was the main physical fouling mechanism, and the cake layer was the main filtration resistance. Specific flux (SF) decreased step by step during the whole period of operation due to membrane fouling and concentration polarization. The quality of the effluent was good and the turbidity remained lower than 0.1 NTU, and the toxic anion, CN{sup -}, could not be detected because of its low concentration, this indicated that the effluent was safe. The AMF process was feasible for practical application in the treatment of liquid waste containing cesium.

  11. Hanford Facility dangerous waste permit application, liquid effluent retention facility and 200 area effluent treatment facility

    Energy Technology Data Exchange (ETDEWEB)

    Coenenberg, J.G.

    1997-08-15

    The Hanford Facility Dangerous Waste Permit Application is considered to 10 be a single application organized into a General Information Portion (document 11 number DOE/RL-91-28) and a Unit-Specific Portion. The scope of the 12 Unit-Specific Portion is limited to Part B permit application documentation 13 submitted for individual, `operating` treatment, storage, and/or disposal 14 units, such as the Liquid Effluent Retention Facility and 200 Area Effluent 15 Treatment Facility (this document, DOE/RL-97-03). 16 17 Both the General Information and Unit-Specific portions of the Hanford 18 Facility Dangerous Waste Permit Application address the content of the Part B 19 permit application guidance prepared by the Washington State Department of 20 Ecology (Ecology 1987 and 1996) and the U.S. Environmental Protection Agency 21 (40 Code of Federal Regulations 270), with additional information needs 22 defined by the Hazardous and Solid Waste Amendments and revisions of 23 Washington Administrative Code 173-303. For ease of reference, the Washington 24 State Department of Ecology alpha-numeric section identifiers from the permit 25 application guidance documentation (Ecology 1996) follow, in brackets, the 26 chapter headings and subheadings. A checklist indicating where information is 27 contained in the Liquid Effluent Retention Facility and 200 Area Effluent 28 Treatment Facility permit application documentation, in relation to the 29 Washington State Department of Ecology guidance, is located in the Contents 30 Section. 31 32 Documentation contained in the General Information Portion is broader in 33 nature and could be used by multiple treatment, storage, and/or disposal units 34 (e.g., the glossary provided in the General Information Portion). Wherever 35 appropriate, the Liquid Effluent Retention Facility and 200 Area Effluent 36 Treatment Facility permit application documentation makes cross-reference to 37 the General Information Portion, rather than duplicating

  12. Coupling of homogeneous liquid-liquid extraction and dispersive liquid-liquid microextraction for the extraction and preconcentration of polycyclic aromatic hydrocarbons from aqueous samples followed by GC with flame ionization detection.

    Science.gov (United States)

    Farajzadeh, Mir Ali; Khiavi, Elahe Behboudi; Khorram, Parisa; Mogaddam, Mohammad Reza Afshar

    2017-01-01

    In the present study, a simple and rapid method for the extraction and preconcentration of some polycyclic aromatic hydrocarbons in water samples has been developed. In this method, two sample preparation methods were combined to obtain high extraction recoveries and enrichment factors for sensitive analysis of the selected analytes. In the first stage of the method, a homogeneous solution containing an aqueous solution and cyclohexyl amine is broken by the addition of a salt. After centrifugation, the upper collected phase containing the extracted analytes is subjected to the following dispersive liquid-liquid microextraction method. Rapid injection of the mixture of cyclohexyl amine resulted from the first stage and 1,1,2-trichloroethane (as an extraction solvent) into an acetic acid solution is led to form a cloudy solution. After centrifuging, the fine droplets of the extraction solvent are settled down in the bottom of the test tube, and an aliquot of it is analyzed by gas chromatography. Under the optimum extraction conditions, enrichment factors and limits of detection for the studied analytes were obtained in the ranges of 616-752 and 0.08-0.20 μg/L, respectively. The simplicity, high extraction efficiency, short sample preparation time, low cost, and safety demonstrated the efficiency of this method relative to other approaches.

  13. Environmentally friendly lycopene purification from tomato peel waste: enzymatic assisted aqueous extraction.

    Science.gov (United States)

    Cuccolini, Stefano; Aldini, Antonio; Visai, Livia; Daglia, Maria; Ferrari, Davide

    2013-02-27

    The antioxidant and anticancer properties of lycopene make it an ideal component for daily food supplements. For this reason this study investigated the possibility of extracting lycopene from tomato waste peels using a green chemistry protocol devoid of organic solvent. Cells are lysed thanks to a combination of pH changes and hydrolytic enzyme treatments. The lycopene-containing chromoplasts are then precipitated by lowering the pH and isolated through a centrifugation step. At this stage the lycopene content of the isolated chromoplasts shows a 10-fold increase (3-5% w/w, dry basis) with respect to untreated tomato peels. A further improvement in lycopene concentration is obtained by a second enzymatic treatment using a protease cocktail. This catalytic step eliminates unwanted proteins, bound to the chromoplasts, but not essential for their stability. The final product shows a lycopene content around 8-10% (w/w, dry basis), which represents a 30-fold increase with respect to the lycopene concentration of the untreated peels.

  14. Removal of heavy metals from aqueous phases using chemically modified waste Lyocell fiber.

    Science.gov (United States)

    Bediako, John Kwame; Wei, Wei; Kim, Sok; Yun, Yeoung-Sang

    2015-12-15

    In this study, an outstanding performance of chemically modified waste Lyocell for heavy metals treatment is reported. The sorbent, which was prepared by a simple and concise method, was able to bind heavy metals such as Pb(II), Cu(II) and Cd(II), with very high efficiencies. The binding mechanisms were studied through adsorption and standard characterization tests such as scanning electron microscopy, energy-dispersive spectroscopy, Fourier transform infrared spectroscopy, and X-ray diffraction analyses. Adsorption kinetics was very fast and attained equilibrium within 5 min in all metals studied. The maximum single metal uptakes were 531.29±0.28 mg/g, 505.64±0.21 mg/g, and 123.08±0.26 mg/g for Pb(II), Cd(II) and Cu(II), respectively. In ternary metal systems, Cu(II) selectivity was observed and the underlying factors were discussed. The sorbent by its nature, could be very effective in treating large volumes of wastewater with the contact of very little amount.

  15. REMOVAL OF ARSENIC FROM AN AQUEOUS SOLUTION BY PRETREATED WASTE TEA FUNGAL BIOMASS

    Directory of Open Access Journals (Sweden)

    S. Mamisahebei , Gh. R. Jahed Khaniki, A. Torabian, S. Nasseri, K. Naddafi

    2007-04-01

    Full Text Available Arsenic contamination in water poses a serious threat on human health. The tea fungus known as Kombucha is a waste produced during black tea fermentation. The objective of this study was to examine the main aspect of a possible strategy for the removal of arsenates employing tea fungal biomass. The pretreatment of biomass with FeCl3 was found to improve the biosorption efficiency. Arsenics uptake was found to be rapid for all concentrations and reached to 79% of equilibrium capacity of biosorption in 20 min and reached equilibrium in 90 min. The pseudo second-order and first-order models described the biosorption kinetics of As (V with good correlation coefficient (R2>0.93 and better than the other equations. The data obtained from the experiment of biosorption isotherm were analyzed using the Freundlich and Langmuir isotherm models. The equation described the isotherm of As (V biosorption with relatively high correlation coefficient (R2>0.93. According to the Langmuir model, the maximum uptake capacities (qm of tea fungal biomass for As (V were obtained 3.9810-3 mmol/gr. The effect of Na+, K+, Mg+2 and Ca+2 on equilibrium capacities of As was not significant. The variation of sorption efficiency with pH showed that optimum biosorption takes place in the pH ranges of 6 to 8. Promising results were obtained in laboratory experiments and effective As (V removals were observed.

  16. Application of coals as sorbents for the removal of Cr from aqueous waste streams

    Energy Technology Data Exchange (ETDEWEB)

    Lakatos, J.; Brown, S.D.; Snape, C.E. [University of Miskolc, Miskolc (Hungary). Dept. of Analytical Chemistry

    2001-09-01

    The study reported further understanding of how various electron transfer processes operate for Cr(VI) with a view to using coals for the removal of Cr(VI) from waste streams. Skye peat, Spanish and German lignites, UK high and low volatility bituminous coals and an activated carbon were used. After treatment to remove exchangeable cations, ion exchange experiments were conducted in 0.1 M acetic acid-sodium acetate (1:1) buffer and 0.05 M sulphuric acid solutions and the slurries were agitated once a day. The ion concentrations in the solutions were determined by flame atomic absorption spectroscopy. The Cr(VI) renaming in solution was determined by the standard calorimetric 1,5-diphenylcarbazide method. Peat and low rank (Spanish Mequinenza) coal exhibited a larger capacity for Cr(VI) removal than bituminous coal. Redox mechanisms are operative coupled with the oxidation of the coal and peat surfaces. Desorption of Cr(III) formed by reduction which occurs in strongly acidic media also needs to be considered. 1 ref., 3 figs.

  17. Enhanced Stability of the Model Mini-protein in Amino Acid Ionic Liquids and Their Aqueous Solutions

    CERN Document Server

    Chevrot, Guillaume; Chaban, Vitaly V

    2015-01-01

    Using molecular dynamics simulations, the structure of model mini-protein was thoroughly characterized in the imidazolium-based amino acid ionic liquids and their aqueous solutions. We report that the mini-protein is more stable when AAIL is added as a cosolvent. Complete substitution of water by organic cations and anions further results in hindered conformational flexibility of the mini-protein. This observation suggests that AAILs are able to defend proteins from thermally induced denaturation. We show by means of radial distributions that the mini-protein is efficiently solvated by both solvents due to agood mutual miscibility. However, amino acid based anions prevail in the first coordination sphere of the mini-protein.

  18. Partitioning of non-ionic surfactants between water and non-aqueous phase liquids (NAPLs) of chlorinated organics

    Science.gov (United States)

    KANG, S.; Jeong, H. Y.

    2013-12-01

    Due to the hydrophobic nature, chlorinated organic compounds penetrate soil and groundwater to form non-aqueous phase liquids (NAPLs). At the sites contaminated with such NAPLs, thus, surfactants are applied to increase the aqueous solubility of chlorinated organics via micellar solubilization. However, a portion of surfactants can be partitioned into NAPL phases by forming reverse micelles within them. Consequently, lesser amounts of surfactants are available for the micellar solubilization of chlorinated organics in the aqueous phase. In this study, we investigated the partitioning behavior of non-ionic surfactants (Tween 20, Tween 40, Tween 80, and Triton X-100) between water and a NAPL phase consisting of tetrachloroethylene (PCE), trichloroethylene (TCE), or chloroform (CF). According to the experimental results, the partitioning of surfactants in the water-NAPL systems was found to follow linear or Langmuir-type isotherms. Regardless of type of surfactants, the partitioning loss of surfactants into NAPLs became greater with the more hydrophilic (i.e., the lower water-NAPL interfacial tension) chlorinated organics: PCE Tween 80 << Triton X-100, suggesting that the greater partitioning occurred with the more hydrophobic (i.e., the lower hydrophilic-lipophilic balance, HLB) surfactant. Consistent with this postulation, the surfactant partitioning into PCE-NAPLs showed the similar trend. In case of TCE-NAPLs, however, the more hydrophobic Tween 40 was partitioned to a less extent than Tween 20. Therefore, the specific interaction of a NAPL-surfactant pair as well as their individual properties should be considered when selecting an effective surfactant for the remediation of a NAPL-contaminated site.

  19. Characterization of aqueous two phase systems by combining lab-on-a-chip technology with robotic liquid handling stations.

    Science.gov (United States)

    Amrhein, Sven; Schwab, Marie-Luise; Hoffmann, Marc; Hubbuch, Jürgen

    2014-11-07

    Over the last decade, the use of design of experiment approaches in combination with fully automated high throughput (HTP) compatible screenings supported by robotic liquid handling stations (LHS), adequate fast analytics and data processing has been developed in the biopharmaceutical industry into a strategy of high throughput process development (HTPD) resulting in lower experimental effort, sample reduction and an overall higher degree of process optimization. Apart from HTP technologies, lab-on-a-chip technology has experienced an enormous growth in the last years and allows further reduction of sample consumption. A combination of LHS and lab-on-a-chip technology is highly desirable and realized in the present work to characterize aqueous two phase systems with respect to tie lines. In particular, a new high throughput compatible approach for the characterization of aqueous two phase systems regarding tie lines by exploiting differences in phase densities is presented. Densities were measured by a standalone micro fluidic liquid density sensor, which was integrated into a liquid handling station by means of a developed generic Tip2World interface. This combination of liquid handling stations and lab-on-a-chip technology enables fast, fully automated, and highly accurate density measurements. The presented approach was used to determine the phase diagram of ATPSs composed of potassium phosphate (pH 7) and polyethylene glycol (PEG) with a molecular weight of 300, 400, 600 and 1000 Da respectively in the presence and in the absence of 3% (w/w) sodium chloride. Considering the whole ATPS characterization process, two complete ATPSs could be characterized within 24h, including four runs per ATPS for binodal curve determination (less than 45 min/run), and tie line determination (less than 45 min/run for ATPS preparation and 8h for density determination), which can be performed fully automated over night without requiring man power. The presented methodology provides

  20. Comparison of Solvation Effects on CO2 Capture with Aqueous Amine Solutions and Amine-Functionalized Ionic Liquids.

    Science.gov (United States)

    Yamada, Hidetaka

    2016-10-13

    Amines are the most widely utilized chemicals for postcombustion CO2 capture, because the reversible reactions between amines and CO2 through their moderate interaction allow effective "catch and release". Usually, CO2 is dissolved in the form of an anion such as carbamate or bicarbonate. Therefore, the reaction energy diagram is potentially governed to a large extent by the polarity of the surrounding solvent. Herein, we compared aqueous amine solutions and amine-functionalized ionic liquids by investigating their dielectric constants and performing an intrinsic reaction coordinate analysis of the CO2 absorption process. Quantum mechanical calculations at the CCSD(T)/6-311++G(d,p)//B3LYP/6-311++G(d,p) level within the continuum solvation model (SMD/IEF-PCM) revealed contrasting dependencies of C-N bond formation on the dielectric constant in those solutions. Amines react with CO2 on an energy surface that is significantly affected by the dielectric constant in conventional aqueous amine solutions, whereas amine-functionalized anions and CO2 form stable C-N bonds with a comparatively lower activation energy regardless of the dielectric constant.

  1. Aggregation behavior and antimicrobial activity of ester-functionalized imidazolium- and pyridinium-based ionic liquids in aqueous solution.

    Science.gov (United States)

    Garcia, M Teresa; Ribosa, Isabel; Perez, Lourdes; Manresa, Angeles; Comelles, Francesc

    2013-02-26

    Two series of long chain imidazolium- and pyridinium-based ionic liquids containing an ester functional group in the alkyl side chain, 3-methyl-1-alkyloxycarbonylmethylimidazolium bromides (C(n)EMeImBr) and 1-alkyloxycarbonylmethylpyridinium bromides (C(n)EPyrBr), were synthesized and their thermal stability, aggregation behavior in aqueous medium, and antimicrobial activity investigated. The introduction of an ester group decreased the thermal stability of the functionalized ILs compared to simple alkyl chain containing ILs (1-alkyl-3-methylimidazolium bromides and 1-alkylpyridinium bromides). Tensiometry, conductimetry, and spectrofluorimetry were applied to study the self-aggregation of the amphiphilic ILs in aqueous solution. The ILs investigated displayed surface activity and the characteristic chain length dependence of the micellization process of surfactants. As compared to simple alkyl chain containing ILs bearing the same hydrocarbon chain, ester-functionalized ILs possess higher adsorption efficiency (pC(20)) and significantly lower critical micelle concentration (cmc) and surface tension at the cmc (γ(cmc)), indicating that the incorporation of an ester group promotes adsorption at the air/water interface and micelle formation. The antimicrobial activity was evaluated against Gram-negative and Gram-positive bacteria and fungi. ILs containing more than eight carbon atoms in the alkyl chain showed antimicrobial activity. Their efficiency as antimicrobial agents increased with the hydrophobicity of the amphiphilic cation being the C(12) homologous the most active compounds. The incorporation of an ester group particularly increased the biological activity against fungi.

  2. Molecular dynamics simulations of the aqueous interface with the [BMI][PF6] ionic liquid: Comparison of different solvent models.

    Science.gov (United States)

    Chevrot, G; Schurhammer, R; Wipff, G

    2006-09-28

    We report a Molecular Dynamics (MD) study of the interface between water and the hygroscopic room temperature Ionic Liquid "IL" [BMI][PF6] (1-butyl-3-methyl-imidazolium hexafluorophosphate), comparing the TIP3P, SPC/E and TIP5P models for water and two IL models where the ions are +/-1 or +/-0.9 charged. A recent MD study (A. Chaumont, R. Schurhammer and G. Wipff, J. Phys. Chem. B, 2005, 109, 18964) showed that using TIP3P water in conjunction with the IL(+/-1) model led to water-IL mixing without forming an interface, whereas a biphasic system could be obtained with the IL(+/-0.9) model. With the TIP5P and SPC/E models, the juxtaposed aqueous and IL phases are found to remain distinct for at least 20 ns. The resulting IL humidity, exaggerated with the IL(+/-1) model, is in better agreement with experiment using the IL(+/-0.9) model. We also report demixing simulations on the "randomly mixed" liquids, using the IL(+/-0.9) model for the ionic liquid. With the three tested water models, the phases separate very slowly ( approximately 20 ns or more) compared to "classical" chloroform-water mixtures (less than 1 ns), leading to biphasic systems similar to those obtained after equilibration of the juxtaposed liquids. The characteristics of the interface (size, polarity, ion orientation, electrostatic potential) are compared with the different models. Possible reasons why, among the three tested water models, the widely-used TIP3P model exaggerates the inter-solvent mixing, are analyzed. The difficulty in computationally and experimentally equilibrating water-IL mixtures is attributed to the slow dynamics and micro-heterogeneity of the IL and to the different states of water in the IL phase.

  3. Use of ionic liquid in leaching process of brass wastes for copper and zinc recovery

    Institute of Scientific and Technical Information of China (English)

    Ayfer Kilicarslan; Muhlis Nezihi Saridede; Srecko Stopic; Bernd Friedrich

    2014-01-01

    Brass ash from the industrial brass manufacturer in Turkey was leached using the solutions of ionic liquid (IL) 1-butyl-3-methyl-imi-dazolium hydrogen sulfate ([bmim]HSO4) at ambient pressure in the presence of hydrogen peroxide (H2O2) and potassium peroxymonosulfate (oxone) as the oxidants. Parameters affecting leaching efficiency, such as dissolution time, IL concentration, and oxidizing agent addition, were investigated. The results show that [bmim]HSO4 is an efficient IL for the brass ash leaching, providing the dissolution efficiencies of 99%for Zn and 24.82%for Cu at a concentration of 50vol%[bmim]HSO4 in the aqueous solution without any oxidant. However, more than 99%of zinc and 82%of copper are leached by the addition of 50vol%H2O2 to the [bmim]HSO4 solution. Nevertheless, the oxone does not show the promising oxidant behavior in leaching using [bmim]HSO4.

  4. Development of the SREX process for the treatment of ICPP liquid wastes

    Energy Technology Data Exchange (ETDEWEB)

    Wood, D.J.; Law, J.D.; Garn, T.G.; Tillotson, R.D.; Tullock, P.A.; Todd, T.A.

    1997-12-01

    The removal of {sup 90}Sr from actual and simulated wastes at the Idaho Chemical Processing Plant (ICPP) at the Idaho National Engineering and Environmental Laboratory (INEEL) has been demonstrated with the SREX process. This solvent extraction process employs the extractant 4{prime},4{prime}(5{prime}) di-(t-butylcyclohexano)-18-crown-6 in 1-octanol or a mixture of tributyl phosphate and a hydrocarbon diluent called Isopar L{reg_sign}. Process flowsheets have been designed for testing in countercurrent experiments with centrifugal contractors. The flowsheets have been designed using batch contract solvent extraction methods. The extraction of Sr as well as other interfering ions has been studied. The effect of various parameters including nitric acid dependence, extractant concentration dependence, hydronium ion concentration, and interferent concentrations upon the extraction efficiency of the process has been evaluated. The radiolysis of the SREX solvent has also been investigated as a function of absorbed gamma radiation. The extraction efficiency of the solvent has been shown to be only slightly dependent upon absorbed dose in the range 0--1,000 kGy. The decontamination of actual sodium-bearing waste and dissolved calcine solutions has been accomplished in batch contact flowsheets. Decontamination factors as high as 10E3 have been obtained with sequential batch contacts. Flowsheets have been developed to accomplish decontamination of the liquid wastes with respect to {sup 90}Sr as well as the removal of Pb and Hg. Pb may be partitioned from the Sr fraction in a separate stripping procedure using ammonium citrate. This work has led to the formulation of countercurrent flowsheets which have been tested in centrifugal contractors with actual waste and reported in the document INEEL/EXT-97-00832.

  5. Development of the SREX Process for the Treatment of ICPP Liquid Wastes

    Energy Technology Data Exchange (ETDEWEB)

    D. J. Wood; Garn, T. G.; J. D. Law; P. A. Tullock; R. D. Tillotson; T. A. Todd

    1997-10-01

    The removal of Sr-90 from actual and simulated wastes at the Idaho Chemical Processing Plant (ICPP) at the Idaho National Engineering and Environmental Laboratory (INEEL) has been demonstrated with the SREX process. This solvent extraction process employs the extractant 4',4' (5') de-(t-butylcyclohexano)-18-crown-6 in 1-octanol or a mixture of tributyl phosphate and a hydrocarbon diluent called Isopar L. This development work is based upon earlier work performed by Horwitz, et al. at Argonne National Laboratory. Process flowsheets have been designed for testing in countercurrent experiments with centrifugal contactors. The flowsheets have been designed using batch contact solvent extraction methods. The extraction of Sr as well as other interfering ions has been studied. The effect of various parameters including nitric acid dependence, extractant concentration dependence, Hydronium ion concentration, and interferent concentrations upon the extraction efficiency of the process has been evaluated. The radiolysis of the SREX solvent has also been investigated as a function of absorbed gamma radiation. The extraction efficiency of the solvent has been shown to be only slightly dependent upon absorbed dose in the range 0-1000 kGy. The decontamination of actual sodium-bearing waste and dissolved calcine solutions has been accomplished in batch contact flowsheets. Decontamination factors as high as 10E3 have been obtained with sequential batch contacts. Flowsheets have been developed to accomplish decontamination of the liquid wastes with respect to Sr-90, as well as the removal of Pb and Hg. Pb may be partitioned from the Sr fraction in a separate stripping procedure using ammonium citrate. This work has led to the formulation of countercurrent flowsheets which have been tested in centrifugal contactors with actual waste and reported in the document INEEL/EXT-97-00832.

  6. Lyophilization -Solid Waste Treatment

    Science.gov (United States)

    Litwiller, Eric; Flynn, Michael; Fisher, John; Reinhard, Martin

    2004-01-01

    This paper discusses the development of a solid waste treatment system that has been designed for a Mars transit exploration mission. The technology described is an energy-efficient lyophilization technique that is designed to recover water from spacecraft solid wastes. Candidate wastes include feces, concentrated brines from water processors, and other solid wastes that contain free water. The system is designed to operate as a stand-alone process or to be integrated into the International Space Station Waste Collection System. In the lyophilization process, water in an aqueous waste is frozen and then sublimed, separating the waste into a dried solid material and liquid water. The sublimed water is then condensed in a solid ice phase and then melted to generate a liquid product. In the subject system the waste solids are contained within a 0.2 micron bio-guard bag and after drying are removed from the system and stored in a secondary container. This technology is ideally suited to applications such as the Mars Reference Mission, where water recovery rates approaching 100% are desirable but production of CO2 is not. The system is designed to minimize power consumption through the use of thermoelectric heat pumps. The results of preliminary testing of a prototype system and testing of the final configuration are provided. A mathematical model of the system is also described.

  7. Measurements of liquid film thickness, concentration, and temperature of aqueous urea solution by NIR absorption spectroscopy

    Science.gov (United States)

    Pan, R.; Jeffries, J. B.; Dreier, T.; Schulz, C.

    2016-01-01

    A multi-wavelength near-infrared (NIR) diode laser absorption sensor has been developed and demonstrated for real-time monitoring of the thickness, solute concentration, and temperature of thin films of urea-water solutions. The sensor monitors the transmittance of three near-infrared diode lasers through the thin liquid film. Film thickness, urea mass fraction, and liquid temperature were determined from measured transmittance ratios of suitable combinations of lasers. Available laser wavelengths were selected depending on the variation of the NIR absorption spectrum of the solution with temperature and solute concentration. The spectral database was measured by a Fourier transform infrared spectrometer in the range 5500-8000 cm-1 for urea solutions between 5 and 40 wt% and temperatures between 298 and 338 K. A prototype sensor was constructed, and the sensor concept was first validated with measurements using a calibration cell providing liquid layers of variable thickness (200-1500 µm), urea mass fraction (5-40 wt%) and temperature (298-318 K). Temporal variations of film thickness and urea concentration were captured during the constant-temperature evaporation of a liquid film deposited on an optically polished heated quartz flat.

  8. Vapor-Liquid-Solid Equilibria of Sulfur Dioxide in Aqueous Electrolyte Solutions

    DEFF Research Database (Denmark)

    Pereda, Selva; Thomsen, Kaj; Rasmussen, Peter

    2000-01-01

    The Extended UNIQUAC model for electrolyte systems, combined with the Soave-Redlich-Kwong equation of state is used to describe the complex vapor-liquid-solid equilibria of sulfur dioxide in electrolyte solutions. Model parameters based on 1500 experimental data points are presented. The paramete...

  9. Graphene oxide reinforced polymeric ionic liquid monolith solid-phase microextraction sorbent for high-performance liquid chromatography analysis of phenolic compounds in aqueous environmental samples.

    Science.gov (United States)

    Sun, Min; Bu, Yanan; Feng, Juanjuan; Luo, Chuannan

    2016-01-01

    A graphene oxide reinforced polymeric ionic liquids monolith was obtained by copolymerization of graphene oxide doped 1-(3-aminopropyl)-3-(4-vinylbenzyl)imidazolium 4-styrenesulfonate monomer and 1,6-di-(3-vinylimidazolium) hexane bihexafluorophosphate cross-linking agent. Coupled to high-performance liquid chromatography, the monolith was used as a solid-phase microextraction sorbent to analyze several phenolic compounds in aqueous samples. Under the optimized extraction and desorption conditions, linear ranges were 5-400 μg/L for 3-nitrophenol, 2-nitrophenol, and 2,5-dichlorophenol and 2-400 μg/L for 4-chlorophenol, 2-methylphenol, and 2,4,6-trichlorophenol (R(2) = 0.9973-0.9988). The limits of detection were 0.5 μg/L for 3-nitrophenol and 2-nitrophenol and 0.2 μg/L for the rest of the analytes. The proposed method was used to determine target analytes in groundwater from an industrial park and river water. None of the analytes was detected. Relative recoveries were in the range of 75.5-113%.

  10. The Glycolysis of Poly(ethylene terephthalate Waste: Lewis Acidic Ionic Liquids as High Efficient Catalysts

    Directory of Open Access Journals (Sweden)

    Mi Lin Zhang

    2013-11-01

    Full Text Available Poly(ethlyene terephthalate waste from a local market was depolymerized by ethylene glycol (EG in the presence of Lewis acidic ionic liquids [Bmim]ZnCl3 and the qualitative analysis showed that bis(hydroxyethyl terephthalate was the main product. Compared with ionic liquid [Bmim]Cl, the Lewis acidic ionic liquids showed highly catalytic activity in the glycolysis of poly(ethylene terephthalate PET. Significantly, the conversion of PET and the yield of bis(hydroxyethyl terephthalate were achieved at 100% and 83.8% with low catalyst ([Bmim]ZnCl3 loading (0.16 wt %. Investigation also showed that the catalytic activity of [Bmim]ZnCl3 was higher than that of [Bmim]MnCl3. Catalyst [Bmim]ZnCl3 can be reused up to five times and 1H-NMR results show that the recovered catalyst is similar to the fresh one. A mechanism of the glycolysis of PET catalyzed by [Bmim]ZnCl3 was proposed.

  11. SODIUM DI-N-DODECYL PHOSPHATE VESICLES IN AQUEOUS-SOLUTION - EFFECTS OF ETHANOL, PROPANOL, AND TETRAHYDROFURAN ON THE GEL TO LIQUID-PHASE TRANSITION

    NARCIS (Netherlands)

    BLANDAMER, MJ; BRIGGS, B; BUTT, MD; WATERS, M; CULLIS, PM; ENGBERTS, JBFN; HOEKSTRA, D; MOHANTY, RK

    1994-01-01

    For aqueous solutions containing vesicles formed by sodium di-n-dodecyl phosphate, the gel to liquid-crystal transition occurs near 35 degrees C, the temperature T-m. When ethanol is added, T-m decreases, but the scan shows evidence of several transitions as more alcohol is added. The effect of adde

  12. Development of Advanced Electrochemical Emission Spectroscopy for Monitoring Corrosion in Simulated DOE Liquid Waste

    Energy Technology Data Exchange (ETDEWEB)

    Digby D. Macdonald; Brian M. Marx; Sejin Ahn; Julio de Ruiz; Balaji Soundararaja; Morgan Smith; and Wendy Coulson

    2008-01-15

    Various forms of general and localized corrosion represent principal threats to the integrity of DOE liquid waste storage tanks. These tanks, which are of a single wall or double wall design, depending upon their age, are fabricated from welded carbon steel and contain a complex waste-form comprised of NaOH and NaNO{sub 3}, along with trace amounts of phosphate, sulfate, carbonate, and chloride. Because waste leakage can have a profound environmental impact, considerable interest exists in predicting the accumulation of corrosion damage, so as to more effectively schedule maintenance and repair. The different tasks that are being carried out under the current program are as follows: (1) Theoretical and experimental assessment of general corrosion of iron/steel in borate buffer solutions by using electrochemical impedance spectroscopy (EIS), ellipsometry and XPS techniques; (2) Development of a damage function analysis (DFA) which would help in predicting the accumulation of damage due to pitting corrosion in an environment prototypical of DOE liquid waste systems; (3) Experimental measurement of crack growth rate, acoustic emission signals and coupling currents for fracture in carbon and low alloy steels as functions of mechanical (stress intensity), chemical (conductivity), electrochemical (corrosion potential, ECP), and microstructural (grain size, precipitate size, etc) variables in a systematic manner, with particular attention being focused on the structure of the noise in the current and its correlation with the acoustic emissions; (4) Development of fracture mechanisms for carbon and low alloy steels that are consistent with the crack growth rate, coupling current data and acoustic emissions; (5) Inserting advanced crack growth rate models for SCC into existing deterministic codes for predicting the evolution of corrosion damage in DOE liquid waste storage tanks; (6) Computer simulation of the anodic and cathodic activity on the surface of the steel samples

  13. Frozen soil barriers for hazardous waste confinement

    Energy Technology Data Exchange (ETDEWEB)

    Dash, J.G.; Leger, R. [Univ. of Washington, Seattle, WA (United States); Fu, H.Y. [Univ. of California, Santa Barbara, CA (United States)

    1997-12-31

    Laboratory and full field measurements have demonstrated the effectiveness of artificial ground freezing for the containment of subsurface hazardous and radioactive wastes. Bench tests and a field demonstration have shown that cryogenic barriers are impenetrable to aqueous and non aqueous liquids. As a result of the successful tests the US Department of Energy has designated frozen ground barriers as one of its top ten remediation technologies.

  14. Isolation of natural red colorants from fermented broth using ionic liquid-based aqueous two-phase systems.

    Science.gov (United States)

    Ventura, Sónia P M; Santos-Ebinuma, Valéria C; Pereira, Jorge F B; Teixeira, Maria F S; Pessoa, Adalberto; Coutinho, João A P

    2013-05-01

    There is a growing demand for natural colorants. This is prompting the search for new alternative and "benign" separation systems allowing higher recoveries, extraction yields, and selectivities. This work investigates the use of aqueous two-phase systems (ATPS) based on ionic liquids as extraction processes for the recovery of red colorants from the fermented broth of Penicillium purpurogenum DPUA 1275. Several ATPS based on quaternary ammonium and imidazolium were studied in this work aiming at separating the red colorants produced from the remaining colorants and contaminant proteins present in the fermented broth. The results suggest that the red colorants can be isolated by an appropriate manipulation of some of the process conditions, such as the use of quaternary ammonium with short alkyl chains, alkaline media, and short tie-line lengths (extraction point systems with lower concentrations of ionic liquid). These conditions allow large partition coefficients for the red colorants (K red = 24.4 ± 2.3), high protein removal (60.7 ± 2.8 %) and selectivity parameters (S red/prot = 10.05).

  15. Enhanced extraction of proteins using cholinium-based ionic liquids as phase-forming components of aqueous biphasic systems.

    Science.gov (United States)

    Quental, Maria V; Caban, Magda; Pereira, Matheus M; Stepnowski, Piotr; Coutinho, João A P; Freire, Mara G

    2015-09-01

    Aqueous biphasic systems (ABS) composed of ionic liquids (ILs) are promising platforms for the extraction and purification of proteins. In this work, a series of alternative and biocompatible ABS composed of cholinium-based ILs and polypropylene glycol were investigated. The respective ternary phase diagrams, tie-lines, tie-line lengths and critical points were determined at 25°C. The extraction performance of these systems for commercial bovine serum albumin (BSA) was then evaluated. The stability of BSA at the IL-rich phase was ascertained by size exclusion high-performance liquid chromatography and Fourier transform infrared spectroscopy. Appropriate ILs lead to the complete extraction of BSA for the IL-rich phase, in a single step, while maintaining the protein's native conformation. Furthermore, to evaluate the performance of these systems when applied to real matrices, the extraction of BSA from bovine serum was additionally carried out, revealing that the complete extraction of BSA was maintained and achieved in a single step. The remarkable extraction efficiencies obtained are far superior to those observed with typical polymer-based ABS. Therefore, the proposed ABS may be envisaged as a more effective and biocompatible approach for the separation and purification of other value-added proteins.

  16. Laboratory development of methods for centralized treatment of liquid low-level waste at Oak Ridge National Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Arnold, W.D.; Bostick, D.T.; Burgess, M.W.; Taylor, P.A.; Perona, J.J.; Kent, T.E.

    1994-10-01

    Improved centralized treatment methods are needed in the management of liquid low-level waste (LLLW) at Oak Ridge National Laboratory (ORNL). LLLW, which usually contains radioactive contaminants at concentrations up to millicurie-per-liter levels, has accumulated in underground storage tanks for over 10 years and has reached a volume of over 350,000 gal. These wastes have been collected since 1984 and are a complex mixture of wastes from past nuclear energy research activities. The waste is a highly alkaline 4-5 M NaNO{sub 3} solution with smaller amounts of other salts. This type of waste will continue to be generated as a consequence of future ORNL research programs. Future LLLW (referred to as newly generated LLLW or NGLLLW) is expected to a highly alkaline solution of sodium carbonate and sodium hydroxide with a smaller concentration of sodium nitrate. New treatment facilities are needed to improve the manner in which these wastes are managed. These facilities must be capable of separating and reducing the volume of radioactive contaminants to small stable waste forms. Treated liquids must meet criteria for either discharge to the environment or solidification for onsite disposal. Laboratory testing was performed using simulated waste solutions prepared using the available characterization information as a basis. Testing was conducted to evaluate various methods for selective removal of the major contaminants. The major contaminants requiring removal from Melton Valley Storage Tank liquids are {sup 90}Sr and {sup 137}Cs. Principal contaminants in NGLLLW are {sup 9O}Sr, {sup 137}Cs, and {sup 106}Ru. Strontium removal testing began with literature studies and scoping tests with several ion-exchange materials and sorbents.

  17. Ionic liquids for extraction of metals and metal containing compounds from communal and industrial waste water.

    Science.gov (United States)

    Fischer, Lisa; Falta, Thomas; Koellensperger, Gunda; Stojanovic, Anja; Kogelnig, Daniel; Galanski, Markus; Krachler, Regina; Keppler, Bernhard K; Hann, Stephan

    2011-10-01

    In a fundamental study the potential of ionic liquids based on quaternary ammonium- and phosphonium cations and thiol-, thioether-, hydroxyl-, carboxylate- and thiocyanate-functionalized anions has been assessed for future application in advanced sewage treatment. The elimination of the metal(oid)s Ag, As, Cd, Cr, Cu, Hg, Ni, Pb, Pt, Sn, Zn and the cancerostatic platinum compounds cisplatin and carboplatin was screened using a liquid phase micro-extraction set-up. The analytical tool-set consisted of ICP-SFMS and LC-ICP-MS for quantification of metal(oid)s and cancerostatic platinum compounds, respectively. The purity of the ILs was assessed for the investigated metal(oid)s on the base of present EU environmental quality standards and was found to be sufficient for the intended use. In model solutions at environmental relevant concentrations extraction efficiencies≥95% could be obtained for Ag, Cu, Hg and Pt with both phosphonium- and ammonium-based ILs bearing sulphur functionality in the form of thiosalicylate and 2-(methylthiobenzoate) anions, as well as with tricaprylmethylammonium thiocyanate within an extraction time of 120 min. All other metals were extracted to a lower extent (7-79%). In the case of cancerostatic platinum compounds a phosphonium-based IL bearing thiosalicylate functionality showed high extraction efficiency for monoaquacisplatin. For the first time, liquid phase micro extraction with ionic liquids was applied to industrial and communal waste water samples. The concentration of all investigated metal(oid)s could be significantly reduced. The degree of elimination varied with the initial concentration of metals, pH and the amount of suspended particulate matter.

  18. Development of Advanced Electrochemical Emission Spectroscopy for Monitoring Corrosion in Simulated DOE Liquid Waste

    Energy Technology Data Exchange (ETDEWEB)

    Digby Macdonald; Brian Marx; Balaji Soundararajan; Morgan Smith

    2005-07-28

    The different tasks that have been carried out under the current program are as follows: (1) Theoretical and experimental assessment of general corrosion of iron/steel in borate buffer solutions by using electrochemical impedance spectroscopy (EIS), ellipsometry and XPS techniques; (2) Development of a damage function analysis (DFA), which would help in predicting the accumulation of damage due to pitting corrosion in an environment prototypical of DOE liquid waste systems; (3) Experimental measurement of crack growth rate, acoustic emission signals, and coupling currents for fracture in carbon and low alloy steels as functions of mechanical (stress intensity), chemical (conductivity), electrochemical (corrosion potential, ECP), and microstructural (grain size, precipitate size, etc) variables in a systematic manner, with particular attention being focused on the structure of the noise in the current and its correlation with the acoustic emissions; (4) Development of fracture mechanisms for carbon and low alloy steels that are consistent with the crack growth rate, coupling current data and acoustic emissions; (5) Inserting advanced crack growth rate models for SCC into existing deterministic codes for predicting the evolution of corrosion damage in DOE liquid waste storage tanks; (6) Computer simulation of the anodic and cathodic activity on the surface of the steel samples in order to exactly predict the corrosion mechanisms; (7) Wavelet analysis of EC noise data from steel samples undergoing corrosion in an environment similar to that of the high level waste storage containers, to extract data pertaining to general, pitting and stress corrosion processes, from the overall data. The work has yielded a number of important findings, including an unequivocal demonstration of the role of chloride ion in passivity breakdown on nickel in terms of cation vacancy generation within the passive film, the first detection and characterization of individual micro fracture

  19. Use of thin film transistor liquid crystal display (TFT-LCD) waste glass in the production of ceramic tiles.

    Science.gov (United States)

    Lin, Kae-Long

    2007-09-05

    In this study, we employ the following operating conditions: varied pressure (25 kgf/cm(2)), sintering temperature (900-1200 degrees C), sintering time (6h), percentage of thin film transistor liquid crystal display (TFT-LCD) waste glass by weight (0-50%) and temperature rising at a rate of 5 degrees C/min, to fabricate clay tiles. The sintering characteristics of the clay blended with TFT-LCD waste glass tiles are examined to evaluate the feasibility of the reuse of TFT-LCD waste glass. TFT-LCD waste glass contains large amounts of glass. The TCLP leaching concentrations all met the ROC EPAs current regulatory thresholds. The addition of TFT-LCD waste glass to the mixture, increased the apparent weight loss. The incorporation of 50% TFT-LCD waste glass resulted in a significant increase in the porosity ratio of the specimens compared to the porosity ratio of the ceramic tile containing TFT-LCD waste glass. The main constituent in both the clay tile and the clay with TFT-LCD waste glass samples is quartz. Increasing the temperature resulted in an increase in the flexural strength and resistance to abrasion in the tiles. The porosity ratio decreases as shrinkage increases. The relation between the porosity ratio and the hardness of the tiles used in the study is also shown.

  20. Quantitative analysis of ammonium salts in coking industrial liquid waste treatment process based on Raman spectroscopy

    Science.gov (United States)

    Cao, Ya-Nan; Wang, Gui-Shi; Tan, Tu; Cai, Ting-Dong; Liu, Kun; Wang, Lei; Zhu, Gong-Dong; Mei, Jiao-Xu

    2016-10-01

    Quantitative analysis of ammonium salts in the process of coking industrial liquid waste treatment is successfully performed based on a compact Raman spectrometer combined with partial least square (PLS) method. Two main components (NH4SCN and (NH4)2S2O3) of the industrial mixture are investigated. During the data preprocessing, wavelet denoising and an internal standard normalization method are employed to improve the predicting ability of PLS models. Moreover, the PLS models with different characteristic bands for each component are studied to choose a best resolution. The internal and external calibration results of the validated model show a mass percentage error below 1% for both components. Finally, the repeatabilities and reproducibilities of Raman and reference titration measurements are also discussed. Project supported by the National Natural Science Foundation of China (Grant Nos. 41405022 and 61475068).

  1. Solidification/stabilisation of liquid oil waste in metakaolin-based geopolymer

    Science.gov (United States)

    Cantarel, V.; Nouaille, F.; Rooses, A.; Lambertin, D.; Poulesquen, A.; Frizon, F.

    2015-09-01

    The solidification/stabilisation of liquid oil waste in metakaolin based geopolymer was studied in the present work. The process consists of obtaining a stabilised emulsion of oil in a water-glass solution and then adding metakaolin to engage the setting of a geopolymer block with an oil emulsion stabilised in the material. Geopolymer/oil composites have been made with various oil fraction (7, 14 and 20 vol.%). The rigidity and the good mechanical properties have been demonstrated with compressive strength tests. Leaching tests evidenced the release of oil from the composite material is very limited whereas the constitutive components of the geopolymer (Na, Si and OH-) are involved into diffusion process.

  2. Efficiency of a blast furnace slag cement for immobilizing simulated borate radioactive liquid waste.

    Science.gov (United States)

    Guerrero, A; Goñi, S

    2002-01-01

    The efficiency of a blast furnace slag cement (Spanish CEM III/B) for immobilizing simulated radioactive borate liquid waste [containing H3BO3, NaCl, Na2SO4 and Na(OH)] has been evaluated by means of a leaching attack in de-mineralized water at the temperature of 40 degrees C over 180 days. The leaching was carried out according to the ANSI/ANS-16.1-1986 test. Moreover, changes of the matrix microstructure were characterized through porosity and pore-size distribution analysis carried out by mercury intrusion porosimetry (MIP), X-ray diffraction (XRD) and thermal analysis (TG). The results were compared with those obtained from a calcium aluminate cement matrix, previously published.

  3. Extraction of Amino-J Acid from Waste-water by Emulsion Liquid Membrane

    Institute of Scientific and Technical Information of China (English)

    潘碌亭

    2006-01-01

    The emulsion liquid membrane technique was used to extract amino-J acid from industrial dye waste-water. The effects of stirring speed, ratio of the emulsion to water (Rew), ratio of the oil to internal phase (Roi) and membrane phase components on the extraction rate were investigated and optimized. The results showed that the extraction rate of amino-J acid approached 97% when the stirring speed was 300 r/min, Rew 1:6, Roi 1:1, trioctylamine (TOA) 3 mL/100 mL kerosene, and methyl-didecyle-alcohol-acrylate (LMA-2) 3 g/100 mL kerosene, respectively. The extraction rate had not changed with the oil phase reused for times.

  4. Preliminary analysis of the ORNL Liquid Low-Level Waste system

    Energy Technology Data Exchange (ETDEWEB)

    Abraham, T.J.; DePaoli, S.M.; Robinson, S.M.; Walker, A.B.

    1994-08-01

    The objective of this report is to summarize the status of the Liquid Low-Level Waste (LLLW) Systems Analysis project. The focus of this project has been to collect and tabulate data concerning the LLLW system, analyze the current LLLW system operation, and develop the information necessary for the development of long-term treatment options for the LLLW generated at ORNL. The data used in this report were collected through a survey of Oak Ridge National Laboratory (ORNL) literature, various letter reports, and a survey of all current LLLW generators. These data are also being compiled in a user friendly database for ORNL-wide distribution. The database will allow the quick retrieval of all information collected on the ORNL LLLW system and will greatly benefit any LLLW analysis effort. This report summarizes the results for the analyses performed to date on the LLLW system.

  5. 30 CFR 250.217 - What solid and liquid wastes and discharges information and cooling water intake information must...

    Science.gov (United States)

    2010-07-01

    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false What solid and liquid wastes and discharges information and cooling water intake information must accompany the EP? 250.217 Section 250.217 Mineral Resources MINERALS MANAGEMENT SERVICE, DEPARTMENT OF THE INTERIOR OFFSHORE OIL AND GAS AND SULPHUR OPERATIONS IN THE OUTER CONTINENTAL SHELF...

  6. 30 CFR 250.248 - What solid and liquid wastes and discharges information and cooling water intake information must...

    Science.gov (United States)

    2010-07-01

    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false What solid and liquid wastes and discharges information and cooling water intake information must accompany the DPP or DOCD? 250.248 Section 250.248 Mineral Resources MINERALS MANAGEMENT SERVICE, DEPARTMENT OF THE INTERIOR OFFSHORE OIL AND GAS AND SULPHUR OPERATIONS IN THE OUTER CONTINENTAL...

  7. Best available technology for the Los Alamos National Laboratory Radioactive Liquid Waste Treatment Facility

    Energy Technology Data Exchange (ETDEWEB)

    Midkiff, W.S.; Romero, R.L.; Suazo, I.L.; Garcia, R.; Parsons, R.M.

    1993-10-15

    The existing Los Alamos National Laboratory TA-50 liquid radioactive waste treatment plant RLWP has been in service for over thirty years, during this period many technical, regulatory, and processing changes have occurred. The existing facility can no longer comply with the demands and requirements for continued operation, and would not be able to comply with anticipated stringent future contaminant discharge limitations. Either a major upgrading or replacement of the existing facility is required. In order to assess the most appropriate means of providing an adequate facility to comply with predicted requirements for Ta-50, this Best Available Technology (BAT) Study was conducted to compare feasible technical and economic alternatives in order to define the most favorable technology configuration. This report consists of eleven sections. Section 1 provides a general introduction and background of the TA-50 operations and the basis for this study. Section 2 provides a technical discussion of the unit processes at TA-50 and several other comparable operations at other DOE sites. Section 3 addresses the evaluation and selection of appropriate treatment processes. Section 4 provides an analysis of environmental issues and concerns. Section 5 presents the rationale for the selection of preferred process configurations. Section 6 is the evaluation of operational issues. Section 7 addresses energy and resource use topics. Section 8 provides an economic analysis, and Section 9 summarizes the evaluation and the identification of the BAT. These sections are augmented by appendices. The report identifies the construction of a new radioactive liquid waste treatment facility as the BAT. Based on the information analyzed for this study, this option appears to provide the best combination of environmental compliance, operability, and economic value.

  8. Batch and semi-continuous anaerobic digestion of food waste in a dual solid-liquid system.

    Science.gov (United States)

    Zhang, Cunsheng; Su, Haijia; Tan, Tianwei

    2013-10-01

    To avoid the inhibition from both of waste oil and high concentrations of cationic elements, anaerobic digestion of food waste in a dual solid-liquid (ADSL) system was examined in this present paper. Results from batch test indicated that a higher methane yield could be obtained in the ADSL system. The methane yield of food solid waste (FSW), food liquid waste (FLW) and raw food waste (RFW) were 643, 659 and 581 mL/g-VS, respectively. In semi-continuous anaerobic digestion, the optimum organic loading rates (OLR) for FSW, FLW and RFW were 9, 4 and 7 g-VS/L/d, respectively. The total methane production of RFW and ADSL systems, based on 1 kg-VS(RFW), were 405 and 460 L, respectively, indicating that the methane production increased by 13.6% in the ADSL system. The optimum C/N ratio, redistribution of metal element and lower content of waste oil in FSW explain the higher methane production.

  9. Solidification/stabilisation of liquid oil waste in metakaolin-based geopolymer

    Energy Technology Data Exchange (ETDEWEB)

    Cantarel, V.; Nouaille, F.; Rooses, A.; Lambertin, D., E-mail: david.lambertin@cea.fr; Poulesquen, A.; Frizon, F.

    2015-09-15

    Highlights: • Formulation with 20 vol.% of oil in a geopolymer have been successful tested. • Oil waste is encapsulated as oil droplets in metakaolin-based geopolymer. • Oil/geopolymer composite present good mechanical performance. • Carbon lixiviation of oil/geopolymer composite is very low. - Abstract: The solidification/stabilisation of liquid oil waste in metakaolin based geopolymer was studied in the present work. The process consists of obtaining a stabilised emulsion of oil in a water-glass solution and then adding metakaolin to engage the setting of a geopolymer block with an oil emulsion stabilised in the material. Geopolymer/oil composites have been made with various oil fraction (7, 14 and 20 vol.%). The rigidity and the good mechanical properties have been demonstrated with compressive strength tests. Leaching tests evidenced the release of oil from the composite material is very limited whereas the constitutive components of the geopolymer (Na, Si and OH{sup −}) are involved into diffusion process.

  10. Hydrocarbonoclastic biofilms based on sewage microorganisms and their application in hydrocarbon removal in liquid wastes.

    Science.gov (United States)

    Al-Mailem, D M; Kansour, M K; Radwan, S S

    2014-07-01

    Attempts to establish hydrocarbonoclastic biofilms that could be applied in waste-hydrocarbon removal are still very rare. In this work, biofilms containing hydrocarbonoclastic bacteria were successfully established on glass slides by submerging them in oil-free and oil-containing sewage effluent for 1 month. Culture-dependent analysis of hydrocarbonoclastic bacterial communities in the biofilms revealed the occurrence of the genera Pseudomonas, Microvirga, Stenotrophomonas, Mycobacterium, Bosea, and Ancylobacter. Biofilms established in oil-containing effluent contained more hydrocarbonoclastic bacteria than those established in oil-free effluent, and both biofilms had dramatically different bacterial composition. Culture-independent analysis of the bacterial flora revealed a bacterial community structure totally different from that determined by the culture-dependent method. In microcosm experiments, these biofilms, when used as inocula, removed between 20% and 65% crude oil, n-hexadecane, and phenanthrene from the surrounding effluent in 2 weeks, depending on the biofilm type, the hydrocarbon identity, and the culture conditions. More of the hydrocarbons were removed by biofilms established in oil-containing effluent than by those established in oil-free effluent, and by cultures incubated in the light than by those incubated in the dark. Meanwhile, the bacterial numbers and diversities were enhanced in the biofilms that had been previously used in hydrocarbon bioremediation. These novel findings pave a new way for biofilm-based hydrocarbon bioremediation, both in sewage effluent and in other liquid wastes.

  11. Characterization and monitoring of 300 Area facility liquid waste streams: 1994 Annual report

    Energy Technology Data Exchange (ETDEWEB)

    Riley, R.G.; Ballinger, M.Y.; Damberg, E.G.; Evans, J.C.; Julya, J.L.; Olsen, K.B.; Ozanich, R.M.; Thompson, C.J.; Vogel, H.R.

    1995-04-01

    This report summarizes the results of characterizing and monitoring the following sources during calendar year 1994: liquid waste streams from Buildings 306, 320, 324, 326, 331, and 3720 in the 300 Area of Hanford Site and managed by the Pacific Northwest Laboratory; treated and untreated Columbia River water (influent); and water at the confluence of the waste streams (that is, end-of-pipe). Data were collected from March to December before the sampling system installation was completed. Data from this initial part of the program are considered tentative. Samples collected were analyzed for chemicals, radioactivity, and general parameters. In general, the concentrations of chemical and radiological constituents and parameters in building wastewaters which were sampled and analyzed during CY 1994 were similar to historical data. Exceptions were the occasional observances of high concentrations of chloride, nitrate, and sodium that are believed to be associated with excursions that were occurring when the samples were collected. Occasional observances of high concentrations of a few solvents also appeared to be associated with infrequent building r eases. During calendar year 1994, nitrate, aluminum, copper, lead, zinc, bis(2-ethylhexyl) phthalate, and gross beta exceeded US Environmental Protection Agency maximum contaminant levels.

  12. Acetone-soluble cellulose acetate extracted from waste blended fabrics via ionic liquid catalyzed acetylation.

    Science.gov (United States)

    Sun, Xunwen; Lu, Canhui; Zhang, Wei; Tian, Dong; Zhang, Xinxing

    2013-10-15

    Isolation of cellulose from waste polyester/cotton blended fabrics (WBFs) is a bottleneck for recycling and exploiting waste textiles. The objective of this study was to provide a new environmental-friendly and efficient approach for extracting cellulose derivatives and polyester from WBFs. A Bronsted acidic ionic liquid (IL) N-methyl-imidazolium bisulfate, [Hmim]HSO4, was used as a novel catalyst for acetylation of cellulose rather than a solvent with the aim to overcome low isolation efficiency associated with the very high viscosity and relatively high costs of ILs. The extraction yield of acetone-soluble cellulose acetate (CA) was 49.3%, which corresponded to a conversion of 84.5% of the cellulose in the original WBFs; meanwhile, 96.2% of the original poly(ethylene terephthalate) (PET) was recovered. The extracted CA was characterized by (1)H NMR, FTIR, XRD and TGA analysis, and the results indicated that high purity acetone-soluble CA and carbohydrate-free PET could be isolated in this manner from WBFs.

  13. Conditioning of sludge produced through chemical treatment of radioactive liquid waste - Operating experiences

    Energy Technology Data Exchange (ETDEWEB)

    Reddy, D. Anji, E-mail: anji@igcar.gov.i [Centralised Waste Management Facility, Nuclear Recycle Group, BARC Facilities, Kalpakkam 603 102, Tamil Nadu (India); Khandelwal, S.K.; Muthiah, R.; Shanmugamani, A.G.; Paul, Biplob; Rao, S.V.S.; Sinha, P.K. [Centralised Waste Management Facility, Nuclear Recycle Group, BARC Facilities, Kalpakkam 603 102, Tamil Nadu (India)

    2010-07-15

    At Centralised Waste Management Facility (CWMF) 160 m{sup 3} of radioactive chemical sludge, generated from treatment of several batches of category-II and category-III radioactive liquid wastes by chemical precipitation method was stored in clariflocculator (CF) for downstream processing. The sludge needed conditioning before disposal. The analysis of the sludge samples collected at different radial locations and depths from the CF showed suspended solid content of 2.37-13.07% and radioactive content of gross {beta}-{gamma} 5000-27,000 Bq/g and {alpha} 100-600 Bq/g. After comparing different options available for conditioning of the sludge based on their technological and economical aspects, it was decided to dewater it using centrifuge before fixing in cement matrix with additives. Process Control Laboratory of CWMF studied the process in detail to optimize the relevant parameters for fixation of the concentrate obtained from centrifuge. Based on these results, conditioning of the stored sludge was undertaken. The process consisted of diluting the sludge with low active effluents/water for homogenisation and facilitating the transfer of sludge, dewatering of the slurry utilising decanter centrifuge, fixation of dewatered concentrate in Ordinary Portland Cement (OPC) with vermiculite as an additive using in-drum mixing method, providing sufficient time for hardening of fixed mass, transportation and safe disposal into Near Surface Disposal Facility (NSDF). Total 150 m{sup 3} of conditioned waste was produced (750 numbers of drums containing cement fixed concentrate). The paper includes the results of the studies conducted on cement fixed concentrate blocks for finding out their compressive strength and leaching characteristics. It also describes the experiences gained from the above operations.

  14. Function and requirement for a waste disloging and conveyance system for the Idaho National Engineering Laboratory high level liquid waste tanks

    Energy Technology Data Exchange (ETDEWEB)

    Mullen, O.D.

    1996-09-10

    In 1990 the U.S. Department of Energy (DOE) Office of Technology Development initiated the Light Duty Utility Arm (LDUA) program to support the Consent Order between the State of Idaho, U.S. Department of Energy, and the Environmental Protection Agency that requires ceasing use of the 11 high-level liquid waste (HLLW) storage tanks at the Idaho Chemical Processing Plant (ICPP).

  15. Effects of hydraulic retention time (HRT) on denitrification using waste activated sludge thermal hydrolysis liquid and acidogenic liquid as carbon sources.

    Science.gov (United States)

    Guo, Yiding; Guo, Liang; Sun, Mei; Zhao, Yangguo; Gao, Mengchun; She, Zonglian

    2017-01-01

    Waste activated sludge (WAS) internal carbon source can efficiently and economically enhance denitrification, and hydraulic retention time (HRT) is one of the most important operational parameters for denitrification. The effects of HRT on denitrification were investigated with WAS thermal hydrolysis liquid and acidogenic liquid as carbon sources in this study. The optimal HRT was 12h for thermal hydrolysis liquid and 8h for acidogenic liquid, with NO3(-)-N removal efficiency of 91.0% and 97.6%, respectively. In order to investigate the utilization of sludge carbon source by denitrifier, the changes of SCOD (Soluble chemical oxygen demand), proteins, carbohydrates, and VFAs (Volatile fatty acids) during denitrification process were analyzed and three-dimensional fluorescence excitation-emission matrix (EEM) spectroscopy with fluorescence regional integration (FRI) analysis was introduced. The kinetics parameters of denitrification rate (VDN), denitrification potential (PDN) and heterotroph anoxic yield (YH) were also investigated using sludge carbon source at different HRT.

  16. Selective extraction and recovery of rare earth metals from phosphor powders in waste fluorescent lamps using an ionic liquid system.

    Science.gov (United States)

    Yang, Fan; Kubota, Fukiko; Baba, Yuzo; Kamiya, Noriho; Goto, Masahiro

    2013-06-15

    The recycling of rare earth metals from phosphor powders in waste fluorescent lamps by solvent extraction using ionic liquids was studied. Acid leaching of rare earth metals from the waste phosphor powder was examined first. Yttrium (Y) and europium (Eu) dissolved readily in the acid solution; however, the leaching of other rare earth metals required substantial energy input. Ionization of target rare earth metals from the waste phosphor powders into the leach solution was critical for their successful recovery. As a high temperature was required for the complete leaching of all rare earth metals, ionic liquids, for which vapor pressure is negligible, were used as an alternative extracting phase to the conventional organic diluent. An extractant, N, N-dioctyldiglycol amic acid (DODGAA), which was recently developed, showed a high affinity for rare earth metal ions in liquid-liquid extraction although a conventional commercial phosphonic extractant did not. An effective recovery of the rare earth metals, Y, Eu, La and Ce, from the metal impurities, Fe, Al and Zn, was achieved from the acidic leach solution of phosphor powders using an ionic liquid containing DODGAA as novel extractant system.

  17. Removal of anionic azo dyes from aqueous solution by functional ionic liquid cross-linked polymer

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Hejun [Key Laboratory of Colloid and Interface Chemistry, Shandong University, Ministry of Education, Jinan 250100 (China); Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province, China West Normal University, Nanchong 637000 (China); Kan, Taotao [CNOOC Energy Technology and Services-oilfield Technology Services Co., Tanggu, Tianjin 300452 (China); Zhao, Siyuan; Qian, Yixia; Cheng, Xiyuan; Wu, Wenli [School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100 (China); Wang, Xiaodong [Shandong Provincial Analysis and Test Center, Jinan 250100 (China); Zheng, Liqiang, E-mail: lqzheng@sdu.edu.cn [Key Laboratory of Colloid and Interface Chemistry, Shandong University, Ministry of Education, Jinan 250100 (China)

    2013-10-15

    Highlights: • Equilibrium, kinetic and thermodynamic of adsorption of dyes onto PDVB-IL was investigated. • PDVB-IL has a high adsorption capacity to treat dyes solution. • Higher adsorption capacity is due to the functional groups of PDVB-IL. • Molecular structure of dyes influences the adsorption capacity. -- Abstract: A novel functional ionic liquid based cross-linked polymer (PDVB-IL) was synthesized from 1-aminoethyl-3-vinylimidazolium chloride and divinylbenzene for use as an adsorbent. The physicochemical properties of PDVB-IL were investigated by Fourier transform infrared spectroscopy, scanning electron microscopy and thermogravimetric analysis. The adsorptive capacity was investigated using anionic azo dyes of orange II, sunset yellow FCF, and amaranth as adsorbates. The maximum adsorption capacity could reach 925.09, 734.62, and 547.17 mg/g for orange II, sunset yellow FCF and amaranth at 25 °C, respectively, which are much better than most of the other adsorbents reported earlier. The effect of pH value was investigated in the range of 1–8. The result shows that a low pH value is found to favor the adsorption of those anionic azo dyes. The adsorption kinetics and isotherms are well fitted by a pseudo second-order model and Langmuir model, respectively. The adsorption process is found to be dominated by physisorption. The introduction of functional ionic liquid moieties into cross-linked poly(divinylbenzene) polymer constitutes a new and efficient kind of adsorbent.

  18. Effect of Humic Acid on Migration, Distribution and Remediation of Dense Non-aqueous Phase Liquids: A laboratory investigation

    Science.gov (United States)

    Cheng, Z.; Wu, J.; Xu, H.; Gao, Y.

    2014-12-01

    Over the last decades, dense non-aqueous phase liquids (DNAPLs) contamination in the subsurface increases with the rapid development of oil industry and becomes the focus of many studies. The migration, distribution and remediation efficiency of DNAPLs in the subsurface environment are greatly affected by the solution chemistry besides the physical heterogeneities of aquifers. Humic acid (HA), which is ubiquitous in natural environments, is a surface active substance exhibiting solubility enhancement behavior for hydrophobic organic compounds such as DNAPLs. Here we reported a laboratory investigation to study the effects of HA on the infiltration, immobilization and subsequent recovery of DNAPL in porous media. Tetrachloroethylene (PCE) was selected as the representative DNAPL in this study. Two-dimensional (2-D) sandbox experiments were conducted to investigate the effects of different HA concentrations on the transport, distribution of PCE and the remediation of PCE using surfactant (Tween 80) flushing in a saturated porous media system. The surfactant flushing of PCE was performed after the PCE transport and distribution had reached equilibrium. A light transmission visualization method with charge-coupled device (CCD) camera was adopted to visualize PCE distribution and quantify its saturation. In addition, the experiments were also designed to gather data for the validation of multiphase flow models. Effluent samples were collected to determine dissolved PCE concentrations. PCE solubilization and PCE-water interfacial tension were experimentally determined in aqueous solutions of varying HA concentrations. The experimental results showed that the presence of HA can have a dramatic impact on PCE flow and entrapment, and significantly improved the recovery of PCE during surfactant enhanced aquifer remediation (SEAR). The findings are of use for better understanding of the migration and entrapment of DNAPLs and developing of SEAR technology.

  19. Separation of four flavonol glycosides from Solanum rostratum Dunal using aqueous two-phase flotation followed by preparative high-performance liquid chromatography.

    Science.gov (United States)

    Chang, Lin; Shao, Qian; Xi, Xingjun; Chu, Qiao; Wei, Yun

    2017-02-01

    Aqueous two-phase flotation followed by preparative high-performance liquid chromatography was used to separate four flavonol glycosides from Solanum rostratum Dunal. In the aqueous two-phase flotation section, the effects of sublation solvent, solution pH, (NH4 )2 SO4 concentration in aqueous solution, cosolvent, N2 flow rate, flotation time, and volumes of the polyethylene glycol phase on the recovery were investigated in detail, and the optimal conditions were selected: 50 wt% polyethylene glycol 1000 ethanol solvent as the flotation solvent, pH 4, 350 g/L of (NH4 )2 SO4 concentration in aqueous phase, 40 mL/min of N2 flow rate, 30 min of flotation time, 10.0 mL of flotation solvent volume, and two times. After aqueous two-phase flotation concentration, the flotation products were purified by preparative high-performance liquid chromatography. The purities of the final products A and B were 98.1 and 99.0%. Product B was the mixture of three compounds based on the analysis of high-performance liquid chromatography at the temperature of 10°C, while product A was hyperoside after the identification by nuclear magnetic resonance. Astragalin, 3'-O-methylquercetin 3-O-β-d-galactopyranoside, and 3'-O-methylquercetin 3-O-β-d-glucopyranoside were obtained with the purity of 93.8, 97.1, and 99.2%, respectively, after the further separation of product B using preparative high-performance liquid chromatography.

  20. Comparative study on copper leaching from waste printed circuit boards by typical ionic liquid acids.

    Science.gov (United States)

    Chen, Mengjun; Huang, Jinxiu; Ogunseitan, Oladele A; Zhu, Nengming; Wang, Yan-min

    2015-07-01

    Waste printed circuit boards (WPCBs) are attracting increasing concerns because the recovery of its content of valuable metallic resources is hampered by the presence of hazardous substances. In this study, we used ionic liquids (IL) to leach copper from WPCBs. [BSO3HPy]OTf, [BSO3HMIm]OTf, [BSO4HPy]HSO4, [BSO4HMim]HSO4 and [MIm]HSO4 were selected. Factors that affect copper leaching rate were investigated in detail and their leaching kinetics were also examined with the comparison of [Bmim]HSO4. The results showed that all six IL acids could successfully leach copper out, with near 100% recovery. WPCB particle size and leaching time had similar influences on copper leaching performance, while IL acid concentration, hydrogen peroxide addition, solid to liquid ratio, temperature, showed different influences. Moreover, IL acid with HSO4(-) was more efficient than IL acid with CF3SO3(-). These six IL acids indicate a similar behavior with common inorganic acids, except temperature since copper leaching rate of some IL acids decreases with its increase. The results of leaching kinetics studies showed that diffusion plays a more important role than surface reaction, whereas copper leaching by inorganic acids is usually controlled by surface reaction. This innovation provides a new option for recovering valuable materials such as copper from WPCBs.

  1. Pyrolysis mechanism for recycle renewable resource from polarizing film of waste liquid crystal display panels.

    Science.gov (United States)

    Wang, Ruixue; Xu, Zhenming

    2014-08-15

    Liquid crystal display (LCD) panels mainly consist of polarizing film, liquid crystal and glass substrates. In this study, a novel pyrolysis model and a pyrolysis mechanism to recover the reusable resource from polarizing film of waste LCD panels was proposed. Polarizing film and its major components, such as cellulose triacetate (TAC) and polyvinyl alcohol (PVA) were pyrolyzed, respectively, to model the pyrolysis process. The pyrolysis process mainly generated a large ratio of oil, a few gases and a little residue. Acetic acid was the main oil product and could be easily recycled. The pyrolysis mechanism could be summarized as follows: (i) TAC, the main component of polarizing film, was heated and generated active TAC with a low polymerization, and then decomposed into triacetyl-d-glucose. (ii) Some triacetyl-d-glucose generated triacetyl-d-mannosan and its isomers through an intramolecular dehydration, while most triacetyl-d-glucose generated the main oil product, namely acetic acid, through a six-member cyclic transition state. (iii) Meanwhile, other products formed through a series of bond cleavage, dehydration, dehydrogenation, interesterification and Diels-Alder cycloaddition. This study could contribute significantly to understanding the polarizing film pyrolysis performance and serve as guidance for the future technological parameters control of the pyrolysis process.

  2. Study on the waste liquid crystal display treatment: focus on the resource recovery.

    Science.gov (United States)

    Wang, Xinying; Lu, Xuebin; Zhang, Shuting

    2013-01-15

    A process combined pyrolysis and acid immersion was proposed in this study to dispose the hazardous liquid crystal display (LCD) waste for recovering valuable resources. The thermogravimetric (TG) analysis and fixed bed pyrolysis were investigated for the polarizing film that was separated from LCD. The results suggested the liquid product mainly contained acids, esters and aromatics should be upgraded such as hydrotreating process before used as industrial feedstock or fuel source. The gaseous product mainly consisted of H(2), CO, CO(2) and CH(4) can be used as a valuable fuel. The sulfuric acid immersion experiments were studied for recovering indium from the LCD glass after stripping the polarizing film. Central composite design (CCD) under response surface methodology (RSM) was used to optimize the acid immersion process and the results indicated the indium recovery can be fitted based on the actual value to a polynomial quadratic equation and the temperature was more essential factor than time and acid concentration in the studied ranges. The optimum processing condition was obtained with time 42.2 min, temperature 65.6 °C and acid concentration 0.6 mol/L. Under the optimal conditions, the indium recovery was close to 100%.

  3. Transport properties investigation of aqueous protic ionic liquid solutions through conductivity, viscosity, and NMR self-diffusion measurements.

    Science.gov (United States)

    Anouti, Mérièm; Jacquemin, Johan; Porion, Patrice

    2012-04-12

    We present a study on the transport properties through conductivity (σ), viscosity (η), and self-diffusion coefficient (D) measurements of two pure protic ionic liquids--pyrrolidinium hydrogen sulfate, [Pyrr][HSO(4)], and pyrrolidinium trifluoroacetate, [Pyrr][CF(3)COO]--and their mixtures with water over the whole composition range at 298.15 K and atmospheric pressure. Based on these experimental results, transport mobilities of ions have been then investigated in each case through the Stokes-Einstein equation. From this, the proton conduction in these PILs follows a combination of Grotthuss and vehicle-type mechanisms, which depends also on the water composition in solution. In each case, the displacement of the NMR peak attributed to the labile proton on the pyrrolidinium cation with the PILs concentration in aqueous solution indicates that this proton is located between the cation and the anion for a water weight fraction lower than 8%. In other words, for such compositions, it appears that this labile proton is not solvated by water molecules. However, for higher water content, the labile protons are in solution as H(3)O(+). This water weight fraction appears to be the solvation limit of the H(+) ions by water molecules in these two PILs solutions. However, [Pyrr][HSO(4)] and [Pyrr][CF(3)COO] PILs present opposed comportment in aqueous solution. In the case of [Pyrr][CF(3)COO], η, σ, D, and the attractive potential, E(pot), between ions indicate clearly that the diffusion of each ion is similar. In other words, these ions are tightly bound together as ion pairs, reflecting in fact the importance of the hydrophobicity of the trifluoroacetate anion, whereas, in the case of the [Pyrr][HSO(4)], the strong H-bond between the HSO(4)(-) anion and water promotes a drastic change in the viscosity of the aqueous solution, as well as on the conductivity which is up to 187 mS·cm(-1) for water weight fraction close to 60% at 298 K.

  4. Development of Advanced Electrochemical Emission Spectroscopy for Monitoring Corrosion in Simulated DOE Liquid Waste

    Energy Technology Data Exchange (ETDEWEB)

    Digby D. Macdonald; Brian M. Marx; Sejin Ahn; Julio de Ruiz; Balaji Soundararaja; Morgan Smith; and Wendy Coulson

    2008-01-15

    Various forms of general and localized corrosion represent principal threats to the integrity of DOE liquid waste storage tanks. These tanks, which are of a single wall or double wall design, depending upon their age, are fabricated from welded carbon steel and contain a complex waste-form comprised of NaOH and NaNO{sub 3}, along with trace amounts of phosphate, sulfate, carbonate, and chloride. Because waste leakage can have a profound environmental impact, considerable interest exists in predicting the accumulation of corrosion damage, so as to more effectively schedule maintenance and repair. The different tasks that are being carried out under the current program are as follows: (1) Theoretical and experimental assessment of general corrosion of iron/steel in borate buffer solutions by using electrochemical impedance spectroscopy (EIS), ellipsometry and XPS techniques; (2) Development of a damage function analysis (DFA) which would help in predicting the accumulation of damage due to pitting corrosion in an environment prototypical of DOE liquid waste systems; (3) Experimental measurement of crack growth rate, acoustic emission signals and coupling currents for fracture in carbon and low alloy steels as functions of mechanical (stress intensity), chemical (conductivity), electrochemical (corrosion potential, ECP), and microstructural (grain size, precipitate size, etc) variables in a systematic manner, with particular attention being focused on the structure of the noise in the current and its correlation with the acoustic emissions; (4) Development of fracture mechanisms for carbon and low alloy steels that are consistent with the crack growth rate, coupling current data and acoustic emissions; (5) Inserting advanced crack growth rate models for SCC into existing deterministic codes for predicting the evolution of corrosion damage in DOE liquid waste storage tanks; (6) Computer simulation of the anodic and cathodic activity on the surface of the steel samples

  5. Pre-concentration and determination of amitriptyline residues in waste water by ionic liquid based immersed droplet microextraction and HPLC

    Institute of Scientific and Technical Information of China (English)

    M.T. Hamed Mosavian; Z. Es'haghi; N. Razavi; S. Banihashemi

    2012-01-01

    This paper describes a new approach for the determination of amitriptyline in wastewater by ionic liquid based immersed droplet microextraction (IL-IDME) prior to highperformance liquid chromatography with ultraviolet detection. 1-Hexyl-3-methylimidazolium hexafluorophosphate ([C6MIM][PF6]) was used as an ionic liquid. Various factors that affect extraction, such as volume of ionic liquid, stirring rate, extraction time, pH of the aqueous solution and salting effect, were optimized. The optimal conditions were as follows: microextraction time, 10 min; stirring rate, 720 rpm; pH, 11; ionic drop volume, 100 uL; and no sodium chloride addition. In quantitative experiments the method showed linearity in a range from 0.01 to 10 ug/mL, a limit of detection of 0.004 ug/mL and an excellent pre-concentration factor (PF) of 1100. Finally, the method was successfully applied to the determination of amitriptyline in the hospital wastewater samples.

  6. Determination of the distribution constants of aromatic compounds and steroids in biphasic micellar phosphonium ionic liquid/aqueous buffer systems by capillary electrokinetic chromatography.

    Science.gov (United States)

    Lokajová, Jana; Railila, Annika; King, Alistair W T; Wiedmer, Susanne K

    2013-09-20

    The distribution constants of some analytes, closely connected to the petrochemical industry, between an aqueous phase and a phosphonium ionic liquid phase, were determined by ionic liquid micellar electrokinetic chromatography (MEKC). The phosphonium ionic liquids studied were the water-soluble tributyl(tetradecyl)phosphonium with chloride or acetate as the counter ion. The retention factors were calculated and used for determination of the distribution constants. For calculating the retention factors the electrophoretic mobilities of the ionic liquids were required, thus, we adopted the iterative process, based on a homologous series of alkyl benzoates. Calculation of the distribution constants required information on the phase-ratio of the systems. For this the critical micelle concentrations (CMC) of the ionic liquids were needed. The CMCs were calculated using a method based on PeakMaster simulations, using the electrophoretic mobilities of system peaks. The resulting distribution constants for the neutral analytes between the ionic liquid and the aqueous (buffer) phase were compared with octanol-water partitioning coefficients. The results indicate that there are other factors affecting the distribution of analytes between phases, than just simple hydrophobic interactions.

  7. Temperature-controlled ionic liquid dispersive liquid phase microextraction combined with ultra-high-pressure liquid chromatography for the rapid determination of triclosan,triclocarban and methyl-triclosan in aqueous samples

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    As extraction solvents,ionic liquids have green characteristics.In this study,an environmentally benign analytical method termed temperature-controlled ionic liquid dispersive liquid phase microextraction (TIL-DLME) combined with ultra-highpressure liquid chromatography (UHPLC)-tunable ultraviolet detection (TUV) was developed for the pre-concentration and determination of triclosan (TCS),triclocarban (TCC) and methyl-triclosan (M-TCS) in water samples.Significant parameters that may affect extraction efficiencies were examined and optimized,including the types and amount of ionic liquids,volume of the diluent,heating temperature,cooling time,salt effect and pH value.Under the optimum conditions,linearity of the method was observed in the ranges of 0.0100-100 μgL-1 for TCS and M-TCS,and 0.00500-50.0 μgL-1 for TCC with correlation coefficients (r2) > 0.9903.The limits of detection (LODs) ranged from 1.15 to 5.33 ngL-1.TCS in domestic water and TCC in reclaimed water were detected at the concentrations of 1.01 and 0.126 μgL-1,respectively.The spiked recoveries of the three target compounds in reclaimed water,irrigating water,waste water and domestic water samples were obtained in the ranges of 68.4%-71.9%,61.6%-87.8%,58.9%-74.9% and 64.9%-92.4%,respectively.Compared with the previous dispersive liquid-liquid microextraction method (DLLME) about the determination of TCS,TCC and M-TCS,this method is not only more environmentally friendly but also more sensitive.

  8. Nitrogen-Doped Porous Carbons from Ionic Liquids@MOF: Remarkable Adsorbents for Both Aqueous and Nonaqueous Media.

    Science.gov (United States)

    Ahmed, Imteaz; Panja, Tandra; Khan, Nazmul Abedin; Sarker, Mithun; Yu, Jong-Sung; Jhung, Sung Hwa

    2017-03-22

    Porous carbons were prepared from a metal-organic framework (MOF, named ZIF-8), with or without modification, via high-temperature pyrolysis. Porous carbons with high nitrogen content were obtained from the calcination of MOF after introducing an ionic liquid (IL) (IL@MOF) via the ship-in-bottle method. The MOF-derived carbons (MDCs) and IL@MOF-derived carbons (IMDCs) were characterized using various techniques and used for liquid-phase adsorptions in both water and hydrocarbon to understand the possible applications in purification of water and fuel, respectively. Adsorptive performances for the removal of organic contaminants, atrazine (ATZ), diuron, and diclofenac, were remarkably enhanced with the modification/conversion of MOFs to MDC and IMDC. For example, in the case of ATZ adsorption, the maximum adsorption capacity of IMDC (Q0 = 208 m(2)/g) was much higher than that of activated carbon (AC, Q0 = 60 m(2)/g) and MDC (Q0 = 168 m(2)/g) and was found to be the highest among the reported results so far. The results of adsorptive denitrogenation and desulfurization of fuel were similar to that of water purification. The IMDCs are very useful in the adsorptions since these new carbons showed remarkable performances in both the aqueous and nonaqueous phases. These results are very meaningful because hydrophobic and hydrophilic adsorbents are usually required for the adsorptions in the water and fuel phases, respectively. Moreover, a plausible mechanism, H-bonding, was also suggested to explain the remarkable performance of the IMDCs in the adsorptions. Therefore, the IMDCs derived from IL@MOF might have various applications, especially in adsorptions, based on high porosity, mesoporosity, doped nitrogen, and functional groups.

  9. Collective dose estimates by the marine food pathway from liquid radioactive wastes dumped in the Sea of Japan.

    Science.gov (United States)

    Togawa, O; Povinec, P P; Pettersson, H B

    1999-09-30

    IAEA-MEL has been engaged in an assessment programme related to radioactive waste dumping by the former USSR and other countries in the western North Pacific Ocean and its marginal seas. This paper focuses on the Sea of Japan and on estimation of collective doses from liquid radioactive wastes. The results from the Japanese-Korean-Russian joint expeditions are summarized, and collective doses for the Japanese population by the marine food pathway are estimated from liquid radioactive wastes dumped in the Sea of Japan and compared with those from global fallout and natural radionuclides. The collective effective dose equivalents by the annual intake of marine products caught in each year show a maximum a few years after the disposals. The total dose from all radionuclides reaches a maximum of 0.8 man Sv in 1990. Approximately 90% of the dose derives from 137Cs, most of which is due to consumption of fish. The total dose from liquid radioactive wastes is approximately 5% of that from global fallout, the contribution of which is below 0.1% of that of natural 210Po.

  10. Recycling acetic acid from polarizing film of waste liquid crystal display panels by sub/supercritical water treatments.

    Science.gov (United States)

    Wang, Ruixue; Chen, Ya; Xu, Zhenming

    2015-05-19

    Waste liquid crystal display (LCD) panels mainly contain inorganic materials (glass substrate) and organic materials (polarizing film and liquid crystal). The organic materials should be removed first since containing polarizing film and liquid crystal is to the disadvantage of the indium recycling process. In the present study, an efficient and environmentally friendly process to obtain acetic acid from waste LCD panels by sub/supercritical water treatments is investigated. Furthermore, a well-founded reaction mechanism is proposed. Several highlights of this study are summarized as follows: (i) 99.77% of organic matters are removed, which means the present technology is quite efficient to recycle the organic matters; (ii) a yield of 78.23% acetic acid, a quite important fossil energy based chemical product is obtained, which can reduce the consumption of fossil energy for producing acetic acid; (iii) supercritical water acts as an ideal solvent, a requisite reactant as well as an efficient acid-base catalyst, and this is quite significant in accordance with the "Principles of Green Chemistry". In a word, the organic matters of waste LCD panels are recycled without environmental pollution. Meanwhile, this study provides new opportunities for alternating fossil-based chemical products for sustainable development, converting "waste" into "fossil-based chemicals".

  11. Analysis of liquid radioactive wastes of Angra-1 reactor; Analise de efluentes liquidos radioativos de Angra-1

    Energy Technology Data Exchange (ETDEWEB)

    Martins, Nadia Soido F.; Peres, Sueli da Silva [Instituto de Radioprotecao e Dosimetria (IRD), Rio de Janeiro, RJ (Brazil); S. Filho, Aluisio Mendes [Central Nuclear Almirante Alvaro Alberto, Angra dos Reis, RJ (Brazil)

    2001-07-01

    Any activity that produces or uses radioactive materials generates radioactive wastes. Normal operation of nuclear power plant produces radioactive waste that can be in gas, liquid or solid form and its level of radioactivity can vary. Gases and liquids wastes are treated and released into environment. The main source of radioactivity released to environment from Angra 1 are liquids from Waste Monitor Tanks. Those releases are under administrative control to meet the discharge limits established by Comissao Nacional de Energia Nuclear (CNEN). A representative sample of each batch is taken for analysis for principal gamma- emitting radionuclides and, if the analysis indicate that release can be made, the quantity of activity is recorded. Within the licensing process of Angra 1, monthly a proportional composite samples are made up with a aliquot of each batch and sent to Instituto de Radioprotecao e Dosimetria (IRD) to analyze and compare with the results reported. This comparative analyses showed that when the activity of that samples was very high, the activity measured on composite samples was higher than the sum of the activities measured on each batch. The operator was advised and requested to identify and solve the problem. This work presents the problem occurred and the solution found to improve the performance of measurements. (author)

  12. Identification and characterization of microorganisms from earthworm viscera for the conversion of fish wastes into liquid fertilizer.

    Science.gov (United States)

    Kim, Joong Kyun; Dao, Van Thingoc; Kong, In Soo; Lee, Hyung Ho

    2010-07-01

    Five bacteria isolated from earthworm viscera and identified as Brevibacillus agri, Bacillus cereus, Bacillus licheniformis, and Brevibacillus parabrevis by 16S rRNA sequencing were employed in the conversion of fish wastes generated from a restaurant specializing in sliced raw fish into fertilizer. Within 120h after inoculation of autoclaved fish waste with 5.15 x 10(5) CFU ml(-1) mixed isolates, the amount of dry sludge decreased from 29.4 to 0.2g, the pH changed from 7.05 to 5.70, and the cell number reached 6.45 x 10(5) CFU ml(-1). Analyses of an 84-h culture of inoculated fish waste indicated low phytotoxicity in a seed germination test, an amino acid content of 5.71 g 100 g(-1), a low concentration of heavy metals (Pb, As, Cd, Hg, Cr, Cu, Ni and Zn), and a N/P/K level of 2.33%. Therefore the converted fish waste has the potential for use as liquid fertilizer, although the low NPK level is a concern. This is the first demonstration of the reutilization of fish wastes as a liquid fertilizer.

  13. NMR investigation of imidazolium-based ionic liquids and their aqueous mixtures.

    Science.gov (United States)

    Cesare Marincola, Flaminia; Piras, Cristina; Russina, Olga; Gontrani, Lorenzo; Saba, Giuseppe; Lai, Adolfo

    2012-04-10

    (1)H and (13)C NMR spectroscopy is employed to investigate the interaction of water with two imidazolium-based ionic liquids (ILs), 1-hexyl-3-methylimidazolium bromide ([C(6)mim]Br) and 1-octyl-3-methylimidazolium bromide ([C(8)mim]Br), at IL concentrations well above the critical aggregation concentration (CAC). The results are compared with those of the neat samples. To this aim, a detailed analysis of the changes in the (1)H chemical shifts, (13)C relaxation parameters, and 2D ROESY data due to the presence of water is performed. The results for both neat ILs are consistent with a packed structure where head-to-head, head-to-tail, and tail-to-tail contacts occur and where the site of maximal mobility restriction is at the polar head. At the lowest investigated water content, the presence of water influences mainly the environment around the IL polar head, slowing down the motional dynamics of the aromatic ring with respect to the alkyl chain. At higher water contents this difference diminishes, the motional freedom of the whole molecule increasing. The presence of ROESY cross-peaks between protons in the polar and apolar IL regions, as well as between protons in non-neighboring alkyl groups, at all investigated water contents suggests that the alkyl tails are not fully segregated in hydrophobic domains, as expected for micelle-like structures.

  14. Self-assembly, Condensation, and Order in Aqueous Lyotropic Chromonic Liquid Crystals Crowded with Additives

    Energy Technology Data Exchange (ETDEWEB)

    Tortora, L.; Park, H; Kang, S; Savaryn, V; Hong, S; Kaznatcheev, K; Finotello, D; Sprunt, S; Kumar, S; Lavrentovich, O

    2010-01-01

    Dense multicomponent systems with macromolecules and small solutes attract a broad research interest as they mimic the molecularly crowded cellular interiors. The additives can condense and align the macromolecules, but they do not change the degree of covalent polymerization. We chose a lyotropic chromonic liquid crystal with reversibly and non-covalently assembled aggregates as a much softer system, reminiscent of 'living polymers', to demonstrate that small neutral and charged additives cause condensation of aggregates with ensuing orientational and positional ordering and nontrivial morphologies of phase separation, such as tactoids and toroids of the nematic and hexagonal columnar phase coexisting with the isotropic melt. Scanning transmission X-ray microscopy (STXM) with near edge X-ray absorption fine structure (NEXAFS) analysis as well as fluorescent microscopy demonstrates segregation of the components. The observations suggest that self-assembly of chromonic aggregates in the presence of additives is controlled by both entropy effects and by specific molecular interactions and provide a new route to the regulated reversible assembly of soft materials formed by low-molecular weight components.

  15. Self-assembly, condensation, and order in aqueous lyotropic chromonic liquid crystals crowded with additives

    Energy Technology Data Exchange (ETDEWEB)

    Tortora, Luana; Park, Heung-Shik; Kang, Shin-Woong; Savaryn, Victoria; Hong, Seung-Ho; Kaznatcheev, Konstantine; Finotello, Daniele; Sprunt, Samuel; Kumar, Satyendra; Lavrentovich, Oleg D. (Chonbuk); (Kent); (BNL)

    2012-09-06

    Dense multicomponent systems with macromolecules and small solutes attract a broad research interest as they mimic the molecularly crowded cellular interiors. The additives can condense and align the macromolecules, but they do not change the degree of covalent polymerization. We chose a lyotropic chromonic liquid crystal with reversibly and non-covalently assembled aggregates as a much softer system, reminiscent of 'living polymers', to demonstrate that small neutral and charged additives cause condensation of aggregates with ensuing orientational and positional ordering and nontrivial morphologies of phase separation, such as tactoids and toroids of the nematic and hexagonal columnar phase coexisting with the isotropic melt. Scanning transmission X-ray microscopy (STXM) with near edge X-ray absorption fine structure (NEXAFS) analysis as well as fluorescent microscopy demonstrates segregation of the components. The observations suggest that self-assembly of chromonic aggregates in the presence of additives is controlled by both entropy effects and by specific molecular interactions and provide a new route to the regulated reversible assembly of soft materials formed by low-molecular weight components.

  16. Aqueous liquid feed organic fuel cell using solid polymer electrolyte membrane

    Science.gov (United States)

    Surampudi, Subbarao (Inventor); Narayanan, Sekharipuram R. (Inventor); Vamos, Eugene (Inventor); Frank, Harvey A. (Inventor); Halpert, Gerald (Inventor); Olah, George A. (Inventor); Prakash, G. K. Surya (Inventor)

    1997-01-01

    A liquid organic fuel cell is provided which employs a solid electrolyte membrane. An organic fuel, such as a methanol/water mixture, is circulated past an anode of a cell while oxygen or air is circulated past a cathode of the cell. The cell solid electrolyte membrane is preferably fabricated from Nafion.TM.. Additionally, a method for improving the performance of carbon electrode structures for use in organic fuel cells is provided wherein a high surface-area carbon particle/Teflon.TM.-binder structure is immersed within a Nafion.TM./methanol bath to impregnate the electrode with Nafion.TM.. A method for fabricating an anode for use in a organic fuel cell is described wherein metal alloys are deposited onto the electrode in an electro-deposition solution containing perfluorooctanesulfonic acid. A fuel additive containing perfluorooctanesulfonic acid for use with fuel cells employing a sulfuric acid electrolyte is also disclosed. New organic fuels, namely, trimethoxymethane, dimethoxymethane, and trioxane are also described for use with either conventional or improved fuel cells.

  17. Solvent extraction of Th(IV) from aqueous solution with methylimidazole in ionic liquid

    Energy Technology Data Exchange (ETDEWEB)

    Li, Wenkui; Lv, Hui; Liu, Ziyi; Wu, Jianrong; Li, Shun; Shen, Yinglin [Lanzhou Univ. (China). Radiochemistry Lab.; Yang, Shenghua [State Key Laboratory of Applied Organic Chemistry, Lanzhou (China)

    2016-07-01

    An extraction of Th(IV) was performed using 1-methylimidazole (1-MIM) or 2-methylimidazole (2-MIM) as the extractant in imidazolium type ionic liquids (ILs) or n-pentanol. The extractability for Th{sup 4+} in ILs was by far higher than that obtained in n-pentanol. The extraction mechanism was determined by slope analysis and ESI-MS. The transfer of Th{sup 4+} with MIM into ILs proceeded through both a cationic exchange and a neutral solvation mechanism, whereas the partitioning of Th{sup 4+} with MIM into n-pentanol only underwent a neutral solvation mechanism. The thermodynamic parameters values (ΔH, ΔS and ΔG) for extraction of Th{sup 4+} with 1-MIM in IL were calculated and the results indicated the extraction reaction was spontaneous and went through endothermic process. Separation of Th{sup 4+} from the solution of lanthanides (III) and uranium was also carried out by 1-MIM in ILs and n-pentanol.

  18. Ionic liquid-based aqueous biphasic systems as a versatile tool for the recovery of antioxidant compounds.

    Science.gov (United States)

    Santos, João H; e Silva, Francisca A; Ventura, Sónia P M; Coutinho, João A P; de Souza, Ranyere L; Soares, Cleide M F; Lima, Álvaro S

    2015-01-01

    The comparative evaluation of distinct types of ionic liquid-based aqueous biphasic systems (IL-ABS) and more conventional polymer/salt-based ABS to the extraction of two antioxidants, eugenol and propyl gallate, is focused. In a first approach, IL-ABS composed of ILs and potassium citrate (C6H5K3O7/C6H8O7) buffer at pH 7 were applied to the extraction of two antioxidants, enabling the assessment of the impact of IL cation core on the extraction. The second approach uses ABS composed of polyethylene glycol (PEG) and potassium phosphate (K2HPO4/KH2PO4) buffer at pH 7 with imidazolium-based ILs as adjuvants. Their application to the extraction of the compounds allowed the investigation of the impact of the presence/absence of IL, the PEG molecular weight, and the alkyl side chain length of the imidazolium cation on the partition. It is possible to maximize the extractive performance of both antioxidants up to 100% using both types of IL-ABS. The IL enhances the performance of ABS technology. The data puts in evidence the pivotal role of the appropriate selection of the ABS components and design to develop a successful extractive process, from both environmental and performance points of view.

  19. A gas/liquid chromatographic-mass spectrometric method for the rapid screening of 250 pesticides in aqueous matrices

    Energy Technology Data Exchange (ETDEWEB)

    Chandramouli, B.; Harvan, D.; Brittain, S.; Hass, R. [Eno River Labs, LLC. Durham, NC (United States)

    2004-09-15

    Pesticide residues in food present a potentially serious and significant cause for concern. Many pesticides have been associated with significant health effects to the nervous and endocrine systems and some have been deemed carcinogenic. There are many well-established techniques for pesticide analysis. However, commercial pesticide methods have traditionally only been available for specific pesticide families, such as chlorinated pesticides or herbicides, and at detection limits ranging from 0.05 ppb to 1 ppm in aqueous matrices. Techniques that can quickly screen for the presence/absence of pesticide residues in food matrices are critical in ensuring the safety of food and water. This paper outlines a combined Gas Chromatographic-High Resolution Mass Spectrometric (GC-HRMS) and Liquid Chromatographic Tandem Mass Spectrometric (LC-MS/MS) screening assay for 250 pesticides that was developed for use in water, and soda samples at screening levels ranging from 0.1-5 ppb. The pesticides selected have been identified by the European Union as being of concern and the target of possible legislation. The list encompasses a variety of pesticide classes and compound groupings.

  20. Detection of non-aqueous phase liquid contamination by SH-TE seismoelectrics: A computational feasibility study

    Science.gov (United States)

    Munch, Federico D.; Zyserman, Fabio I.

    2016-07-01

    In this work we propose a one dimensional numerical study of the seismoelectric signals produced in a fresh water aquifer contaminated by either light or dense non-aqueous phase liquids ((L/D)NAPLs), considering a pure SH-wave seismic source. We investigate the nature of the electromagnetic response generated at media interfaces, the so called Interface Response (IR), by comparing it with the electromagnetic field generated by a current sheet; wherefrom we are able to interpret that the source of the IR behaves as an electric current flowing along the interface, differently to what happens when the IR is originated by the action of a P-wave, where electric charge accumulation generates an electric dipole. We perform a parametric study to analyze how the presence of contaminants affects the IR, resorting to an effective media approach to compute mechanical and electromagnetic properties, and considering three different effective fluid-saturation dependent electrokinetic coupling coefficient models. We observe, as expected, that porosity plays an important role in the amplitude of the IRs. When considering different NAPL saturations, significant effects on the IRs are only seen when the thickness of the contaminated layer is above a threshold value, which depends on the present contaminant and the considered effective electrokinetic coupling coefficient model.

  1. Improving the extraction and purification of immunoglobulin G by the use of ionic liquids as adjuvants in aqueous biphasic systems.

    Science.gov (United States)

    Ferreira, Ana M; Faustino, Vânia F M; Mondal, Dibyendu; Coutinho, João A P; Freire, Mara G

    2016-10-20

    Immunoglobulins G (IgG) could become widespread biopharmaceuticals if cost-efficient processes for their extraction and purification are available. In this work, aqueous biphasic systems (ABS) composed of polyethylene glycols and a buffered salt, and with ionic liquids (ILs) as adjuvants, have been studied as alternative extraction and purification platforms of IgG from a rabbit serum source. Eleven ILs were investigated to provide insights on the chemical features which maximize the IgG partitioning. It is shown that in polymer-salt systems pure IgG preferentially partitions to the polymer-rich phase; yet, the complete extraction was never attained. Remarkably, after the addition of 5wt% of adequate ILs to polymer-salt ABS, the complete extraction of pure IgG in a single-step was accomplished. The best systems and conditions were then applied to the extraction and purification of IgG directly from rabbit serum samples. The complete extraction of IgG in a single-step was maintained while its purity in the polymer-rich phase was enhanced by ca. 37% as compared to the IL-free ABS. The antibody stability was also evaluated revealing that appropriate ILs are able to maintain the IgG stability and can be used as phase-forming components of ABS when envisaging the purification of high-cost biopharmaceuticals.

  2. Tracer test for the measurement of gas diffusion and non-aqueous phase liquid (NAPL) saturation in soil.

    Science.gov (United States)

    Van De Steene, Joke; Höhener, Patrick

    2009-01-01

    During soil bioremediation, the diffusion of oxygen into the soil is an important prerequisite for aerobic biodegradation, and the decrease of petroleum products is the ultimate goal. Both processes need to be monitored. The aim of this work was to develop a gas tracer test that yields information on both, gas diffusion and residual saturation with non-aqueous phase liquids (NAPLs) in unsaturated soil heaps. One conservative tracer (methane) and 4 partitioning gas tracers (diethylether, methyl tert-butyl ether, chloroform and n-heptane) were injected as vapors into laboratory columns filled with unsaturated sand with increasing NAPL saturation. Breakthrough curves of gaseous compounds were measured at two points and compared to analytical solutions of an analytical diffusive-reactive transport equation. By fitting of methane data, robust results for effective diffusivity (tortuosity) were obtained. NAPL saturation was most accurately measured by the moderately water soluble tracers (ethers and chloroform). The hydrophobic tracer n-heptane did not partition into water-immersed NAPL. An easy and accurate way to assess air-NAPL partitioning constants from gas chromatography retention times is furthermore reported. It is concluded that gas tracer tests have the potential for measuring two important properties in soil bioremediation systems easily and quickly.

  3. Interaction between amphiphilic ionic liquid 1-butyl-3-methylimidazolium octyl sulfate and anionic polymer of sodium polystyrene sulfonate in aqueous medium

    Science.gov (United States)

    Barhoumi, Z.; Saini, M.; Amdouni, N.; Pal, A.

    2016-09-01

    The micellization of an aqueous solution of the surface active ionic liquid (SAIL), 1-butyl-3-methylimidazolium octylsufate (C4mim)(C8OSO3) and its interaction with an anionic polymer sodium polystyrene sulfonate, (NaPSS) were studied using conductimetry, tensiometry and fluorimetry. Surface tension profile shows a more dramatic increase in the value of surface tension of aqueous (C4mim)(C8OSO3) before the critical micelle concentration (cmc) of IL. The critical micelle concentration (cmc) value of this surfactant was found out from conductance measurements. The thermodynamic parameters, i.e., Gibb's free energy, enthalpy, and entropy of micellization of the IL in aqueous solution have been calculated. Behavior of fluorescence probe confirms the binding interactions between SAIL and the polyelectrolyte.

  4. Catalytic hydrogenation of aromatic nitro compounds by functionalized ionic liquids-stabilized nickel nanoparticles in aqueous phase:The influence of anions

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Two kinds of nickel nanoparticles (NPs) well-dispersed in aqueous phase have been conveniently prepared by reducing nickel(II) salt with hydrazine in the presence of amino group (-NH2) functionalized ionic liquids:1-(3-aminopropyl)-2,3-dimethylimidazolium bromide ([AMMIM][Br]) and 1-(3-aminopropyl)-2,3-dimethylimidazolium acetate ([AMMIM][AcO]).The Ni(0) particles are composed of smaller ones which assemble in a blackberry-like shape.The Ni nanoparticles stabilized with [AMMIM][AcO] are much larger than those stabilized with [AMMIM][Br],and the former unexpectedly give much higher activity in the selective hydrogenation of citral and nitrobenzene (NB) in aqueous phase.The Ni(0) nanocatalysts dispersed in aqueous phase are stable enough to be reused at least five times without significant loss of catalytic activity and selectivity during the catalytic recycles.

  5. PLUTONIUM FINISHING PLANT (PFP) 241-Z LIQUID WASTE TREATMENT FACILITY DEACTIVATION AND DEMOLITION

    Energy Technology Data Exchange (ETDEWEB)

    JOHNSTON GA

    2008-01-15

    Fluor Hanford, Inc. (FH) is proud to submit the Plutonium Finishing Plant (PFP) 241-Z liquid Waste Treatment Facility Deactivation and Demolition (D&D) Project for consideration by the Project Management Institute as Project of the Year for 2008. The decommissioning of the 241-Z Facility presented numerous challenges, many of which were unique with in the Department of Energy (DOE) Complex. The majority of the project budget and schedule was allocated for cleaning out five below-grade tank vaults. These highly contaminated, confined spaces also presented significant industrial safety hazards that presented some of the most hazardous work environments on the Hanford Site. The 241-Z D&D Project encompassed diverse tasks: cleaning out and stabilizing five below-grade tank vaults (also called cells), manually size-reducing and removing over three tons of process piping from the vaults, permanently isolating service utilities, removing a large contaminated chemical supply tank, stabilizing and removing plutonium-contaminated ventilation ducts, demolishing three structures to grade, and installing an environmental barrier on the demolition site . All of this work was performed safely, on schedule, and under budget. During the deactivation phase of the project between November 2005 and February 2007, workers entered the highly contaminated confined-space tank vaults 428 times. Each entry (or 'dive') involved an average of three workers, thus equaling approximately 1,300 individual confined -space entries. Over the course of the entire deactivation and demolition period, there were no recordable injuries and only one minor reportable skin contamination. The 241-Z D&D Project was decommissioned under the provisions of the 'Hanford Federal Facility Agreement and Consent Order' (the Tri-Party Agreement or TPA), the 'Resource Conservation and Recovery Act of 1976' (RCRA), and the 'Comprehensive Environmental Response, Compensation, and

  6. A novel bio-adsorbent of mint waste for dyes remediation in aqueous environments: study and modeling of isotherms for removal of methylene Blue

    Directory of Open Access Journals (Sweden)

    Tarik Ainane

    2014-09-01

    Full Text Available The objective of this study was to investigate the possibility of using mint waste as a bioadsorbent for the removal of dye (Methylen Blue from aqueous solutions. Batch adsorption studies were carried out by monitoring the pH, the bio-adsorbent dose and the initial dye concentration. Attempts have also been made to monitor the adsorption process through Langmuir, Freundlich, Dubinin-Radushkevich, and Temkin adsorption isotherm models. These results have demonstrated the immense potential of mint waste as a bioadsorbent for dyes remediation in polluted water and wastewater. Finally followed by the process of adsorption phenomenon was achieved by fourier transform infrared spectrometer (FTIR, the results shows that the adsorption is mechanical trapping.

  7. Photoelectron spectroscopy of aqueous solutions: streaming potentials of NaX (X = Cl, Br, and I) solutions and electron binding energies of liquid water and X-.

    Science.gov (United States)

    Kurahashi, Naoya; Karashima, Shutaro; Tang, Ying; Horio, Takuya; Abulimiti, Bumaliya; Suzuki, Yoshi-Ichi; Ogi, Yoshihiro; Oura, Masaki; Suzuki, Toshinori

    2014-05-07

    The streaming potentials of liquid beams of aqueous NaCl, NaBr, and NaI solutions are measured using soft X-ray, He(I), and laser multiphoton ionization photoelectron spectroscopy. Gaseous molecules are ionized in the vicinity of liquid beams and the photoelectron energy shifts are measured as a function of the distance between the ionization point and the liquid beam. The streaming potentials change their polarity with concentration of electrolytes, from which the singular points of concentration eliminating the streaming potentials are determined. The streaming currents measured in air also vanish at these concentrations. The electron binding energies of liquid water and I(-), Br(-), and Cl(-) anions are revisited and determined more accurately than in previous studies.

  8. Impact of ionic liquids in aqueous solution on bacterial plasma membranes studied with molecular dynamics simulations.

    Science.gov (United States)

    Lim, Geraldine S; Zidar, Jernej; Cheong, Daniel W; Jaenicke, Stephan; Klähn, Marco

    2014-09-04

    The impact of five different imidazolium-based ionic liquids (ILs) diluted in water on the properties of a bacterial plasma membrane is investigated using molecular dynamics (MD) simulations. Cations considered are 1-octyl-3-methylimidazolium (OMIM), 1-octyloxymethyl-3-methylimidazolium (OXMIM), and 1-tetradecyl-3-methylimidazolium (TDMIM), as well as the anions chloride and lactate. The atomistic model of the membrane bilayer is designed to reproduce the lipid composition of the plasma membrane of Gram-negative Escherichia coli. Spontaneous insertion of cations into the membrane is observed in all ILs. Substantially more insertions of OMIM than of OXMIM occur and the presence of chloride reduces cation insertions compared to lactate. In contrast, anions do not adsorb onto the membrane surface nor diffuse into the bilayer. Once inserted, cations are oriented in parallel to membrane lipids with cation alkyl tails embedded into the hydrophobic membrane core, while the imidazolium-ring remains mostly exposed to the solvent. Such inserted cations are strongly associated with one to two phospholipids in the membrane. The overall order of lipids decreased after OMIM and OXMIM insertions, while on the contrary the order of lipids in the vicinity of TDMIM increased. The short alkyl tails of OMIM and OXMIM generate voids in the bilayer that are filled by curling lipids. This cation induced lipid disorder also reduces the average membrane thickness. This effect is not observed after TDMIM insertions due to the similar length of cation alkyl chain and the fatty acids of the lipids. This lipid-mimicking behavior of inserted TDMIM indicates a high membrane affinity of this cation that could lead to an enhanced accumulation of cations in the membrane over time. Overall, the simulations reveal how cations are inserted into the bacterial membrane and how such insertions change its properties. Moreover, the different roles of cations and anions are highlighted and the fundamental

  9. Strategies of Learning Graduate Level Experiments and Its Application for the Removal of Toxic Waste Related To Mutual Solubility of Liquids and Phase Coexistence

    Directory of Open Access Journals (Sweden)

    *H. Tahir

    2012-06-01

    Full Text Available This paper describes graduate chemistry practical related to mutual solubility of liquids and phase coexistence. The diversity of the phase transition shows that heating produces mixing and separation. The practical consists of short experiment on the general theme of miscibility of aqueous and organic phases by varying the temperature. The phases were selected as phenol - water and nicotine- water system. The experiment was preceded by the interaction of equal quantities of phenol-water and nicotine-water at room temperature and higher temperature about 80°C. There was a change in miscibility of phases at higher temperature. At about 80°C the phenol-water mixture becomes monophasic while it is heterogeneous at room temperature. The water – phenol phase show limited miscibility below 70 °C. While the nicotine -water phases become heterogenous at higher temperature and at room temperature they were monophasic. The temperature at which these phases were merges is known as clearing temperature or cloud temperature. It lies on the liquid-liquid coexistence line. The experiment required careful observations by students at various temperatures ranges from 20oC to 100oC at the step of 20 0C and followed by result and discussions. Analysis of the data predicted that students were enjoying by working out the practical and it would be bestowing tremendously beneficial learning experience. The aim of this study was to explore the concept of the phenomenon of phase changes by varying the temperatures and can interpret macroscopic and microscopic properties of the system by relating to the thermodynamic properties. These experiments were beneficial for the isolation and separation of toxic compounds like nicotine and phenol from the waste stream. It is effective and low cost method to save the environment and ecosystem.

  10. Effect of alkyl chain length and temperature on the thermodynamic properties of ionic liquids 1-alkyl-3-methylimidazolium bromide in aqueous and non-aqueous solutions at different temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Sadeghi, Rahmat [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of)], E-mail: rahsadeghi@yahoo.com; Shekaari, Hemayat [Department of Chemistry, Faculty of Science, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of); Hosseini, Rahim [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of)

    2009-02-15

    The alkyl chain length of 1-alkyl-3-methylimidazolium bromide ([Rmim][Br], R = propyl (C{sub 3}), hexyl (C{sub 6}), heptyl (C{sub 7}), and octyl (C{sub 8})) was varied to prepare a series of room-temperature ionic liquids (RTILs), and experimental measurements of density and speed of sound at different temperatures ranging from (288.15 to 308.15) K for their aqueous and methanolic solutions in the dilute concentration region (0.01 to 0.30) mol . kg{sup -1} were taken. The values of the compressibilities, expansivity and apparent molar properties for [C{sub n}mim][Br] in aqueous and methanolic solutions were determined at the investigated temperatures. The obtained apparent molar volumes and apparent molar isentropic compressibilities were fitted to the Redlich-Mayer and the Pitzer's equations from which the corresponding infinite dilution molar properties were obtained. The values of the infinite dilution molar properties were used to obtain some information about solute-solvent and solute-solute interactions. The thermodynamic properties of investigated ionic liquids in aqueous solutions have been compared with those in methanolic solutions. Also, the comparison between thermodynamic properties of investigated solutions and those of electrolyte solutions, polymer solutions, cationic surfactant solutions and tetraalkylammonium salt solutions have been made.

  11. Modeling of (vapor + liquid) equilibrium and enthalpy of solution of carbon dioxide (CO{sub 2}) in aqueous methyldiethanolamine (MDEA) solutions

    Energy Technology Data Exchange (ETDEWEB)

    Arcis, Hugues; Rodier, Laurence; Ballerat-Busserolles, Karine [Thermodynamique et Interactions Moleculaires, FRE3099, Universite Blaise Pascal Clermont-Ferrand, CNRS, 24 av. des Landais, 63177 Aubiere (France); Coxam, Jean-Yves [Thermodynamique et Interactions Moleculaires, FRE3099, Universite Blaise Pascal Clermont-Ferrand, CNRS, 24 av. des Landais, 63177 Aubiere (France)], E-mail: j-yves.coxam@univ-bpclermont.fr

    2009-06-15

    A thermodynamic model was used to estimate enthalpy of solution of carbon dioxide (CO{sub 2}) in methyldiethanolamine (MDEA) aqueous solutions. The model was based on a set of equations for chemical equilibria, phase equilibria, charge, and mass balances. Non-ideality in the liquid phase was taken into account by interaction parameters fitted to (vapor + liquid) equilibrium data. The enthalpies of solution of CO{sub 2} were derived from the model using classical thermodynamic relations and were compared to experimental values obtained in previous works.

  12. SAVANNAH RIVER SITE INCIPIENT SLUDGE MIXING IN RADIOACTIVE LIQUID WASTE STORAGE TANKS DURING SALT SOLUTION BLENDING

    Energy Technology Data Exchange (ETDEWEB)

    Leishear, R.; Poirier, M.; Lee, S.; Steeper, T.; Fowley, M.; Parkinson, K.

    2011-01-12

    This paper is the second in a series of four publications to document ongoing pilot scale testing and computational fluid dynamics (CFD) modeling of mixing processes in 85 foot diameter, 1.3 million gallon, radioactive liquid waste, storage tanks at Savannah River Site (SRS). Homogeneous blending of salt solutions is required in waste tanks. Settled solids (i.e., sludge) are required to remain undisturbed on the bottom of waste tanks during blending. Suspension of sludge during blending may potentially release radiolytically generated hydrogen trapped in the sludge, which is a safety concern. The first paper (Leishear, et. al. [1]) presented pilot scale blending experiments of miscible fluids to provide initial design requirements for a full scale blending pump. Scaling techniques for an 8 foot diameter pilot scale tank were also justified in that work. This second paper describes the overall reasons to perform tests, and documents pilot scale experiments performed to investigate disturbance of sludge, using non-radioactive sludge simulants. A third paper will document pilot scale CFD modeling for comparison to experimental pilot scale test results for both blending tests and sludge disturbance tests. That paper will also describe full scale CFD results. The final paper will document additional blending test results for stratified layers in salt solutions, scale up techniques, final full scale pump design recommendations, and operational recommendations. Specifically, this paper documents a series of pilot scale tests, where sludge simulant disturbance due to a blending pump or transfer pump are investigated. A principle design requirement for a blending pump is UoD, where Uo is the pump discharge nozzle velocity, and D is the nozzle diameter. Pilot scale test results showed that sludge was undisturbed below UoD = 0.47 ft{sup 2}/s, and that below UoD = 0.58 ft{sup 2}/s minimal sludge disturbance was observed. If sludge is minimally disturbed, hydrogen will not be

  13. Ionic liquid and aqueous two-phase extraction based on salting-out coupled with high-performance liquid chromatography for the determination of seven rare ginsenosides in Xue-Sai-Tong injection.

    Science.gov (United States)

    Li, Lan-Jie; Jin, Yong-Ri; Wang, Xiao-Zhong; Liu, Ying; Wu, Qian; Shi, Xiao-Lei; Li, Xu-Wen

    2015-09-01

    A method of ionic liquid salt aqueous two-phase extraction coupled with high-performance liquid chromatography has been developed for the analysis of seven rare ginsenosides including Rg6 , F4 , 20(S)-Rg3 , 20(R)-Rg3 , Rk3 , Rk1 , and Rg5 in Xue-Sai-Tong injection. The injection was mixed with ionic liquid 1-butyl-3-methylimidazolium bromide aqueous solution, and a mixture was obtained. With the addition of sodium dodecyl sulfate and dipotassium phosphate into the mixture, the aqueous two-phase mixture was formed after ultrasonic treatment and centrifuged. Rare ginsenosides were extracted into the upper phase. To obtain a high extraction factors, various influences were considered systematically, such as the volume of ionic liquid, the category and amount of salts, the amount of sodium dodecyl sulfate, the pH value of system, and the time of ultrasonic treatment. Under the optimal condition, rare ginsenosides in Xue-Sai-Tong injection were enriched and detected, the recoveries of seven rare ginsenosides ranged from 90.05 to 112.55%, while relative standard deviations were lower than 2.50%. The developed method was reliable, rapid and sensitive for the determination of seven rare ginsenosides in the injections.

  14. Scaled-up bioconversion of fish waste to liquid fertilizer using a 5 L ribbon-type reactor.

    Science.gov (United States)

    Dao, Van Thingoc; Kim, Joong Kyun

    2011-10-01

    A scaled-up conversion process of fish waste to liquid fertilizer was performed in a 5 L ribbon-type reactor. Biodegradation was performed by inoculation of autoclaved fish waste with 5.84 × 10(5) CFU mL(-1) of mixed microorganisms for 96 h. As a result, the pH changed from 6.92 to 5.72, the cell number reached 7.28 × 10(5) CFU mL(-1), and approximately 430 g (28.3%) of fish waste was degraded. Analyses indicated that the 96 h culture of inoculated fish waste possessed comparable fertilizing ability to commercial fertilizers in hydroponic culture with amino acid contents of 6.91 g 100 g(-1). Therefore, the scaled-up production achieved a more satisfactory fish waste degradation rate (3.61 g h(-1)) than the flask-scale production (0.24 g h(-1)). The biodegraded broth of fish waste at room temperature did not undergo putrefaction for 6 months due to the addition of 1% lactate.

  15. Liquid-Phase Synthesis of Ba2V2O7 Phosphor Powders and Films Using Immiscible Biphasic Organic-Aqueous Systems.

    Science.gov (United States)

    Takahashi, Mami; Hagiwara, Manabu; Fujihara, Shinobu

    2016-08-15

    A liquid-phase synthesis of inorganic phosphor materials at a moderate temperature was proposed by using immiscible liquid-liquid biphasic systems. A self-activated Ba2V2O7 phosphor was actually synthesized from vanadium alkoxide dissolved in an organic solution and barium acetate in an aqueous solution. A mild hydrolysis reaction of the alkoxide started at the organic-inorganic interface, and an intermediate compound, Ba(VO3)2·H2O, was initially formed. Ba2V2O7 powders were then obtained by the conversion from Ba(VO3)2·H2O promoted in the aqueous solution. Ba2V2O7 films were obtained on surface-modified silica glass substrates through the similar chemical reactions. Factors such as the surface state of substrates, the kind of organic solvents, and the volume of aqueous solutions were examined to improve the film deposition behavior. The resultant Ba2V2O7 materials showed broad-band visible photoluminescence upon irradiation with ultraviolet light based on the charge transfer transition in the VO4(3-) units existing as dimers.

  16. Ionic Liquid Surfactant Mediated Structural Transitions and Self-Assembly of Bovine Serum Albumin in Aqueous Media: Effect of Functionalization of Ionic Liquid Surfactants.

    Science.gov (United States)

    Singh, Gurbir; Kang, Tejwant Singh

    2015-08-20

    The self-assembly of globular protein bovine serum albumin (BSA) has been investigated in aqueous solutions of ionic liquid surfactants (ILSs), 1-dodecyl-3-methyl imidazolium chloride, [C12mim][Cl], and its amide, [C12Amim][Cl], and ester, [C12Emim][Cl], functionalized counterparts. Dynamic light scattering (DLS) has provided insights into the alterations in hydrodynamic radii (D(h)) of BSA as a function of concentration of ILSs establishing the presence of different types of BSA-ILS complexes in different concentration regimes of ILSs. Isothermal titration calorimetry (ITC) has been exploited to quantify the ILSs interacting with BSA in dilute concentration regime of ILSs. The zeta-potential measurements shed light on changes in the charged state of BSA. The morphology of various self-assembled structures of BSA in different concentration regimes of ILSs have been explored using confocal laser scanning microscopy (CLSM) and scanning electron microscopy. The structural variations in ILSs have been found to produce remarkable effect on the nature and morphology of self-assembled structures of BSA. The presence of nonfunctionalized [C12mim][Cl] IL at all investigated concentrations has led to the formation of unordered large self-assembled structures of BSA. On the other hand, in specific concentration regimes, ordered self-assembled structures such as long rods and right-handedly twisted helical amyloid fibers have been observed in the presence of functionalized [C12Amim][Cl] and [C12Emim][Cl] ILSs, respectively. The nature of the formed helical fibers as amyloid ones has been confirmed using FTIR spectroscopy. Steady-state fluorescence and circular dichroism (CD) spectroscopy have provided insights into folding and unfolding of BSA as fashioned by interactions with ILSs in different concentration regimes supporting the observations made from other studies.

  17. Inductively coupled plasma torch efficiency at atmospheric pressure for organo-chlorine liquid waste removal: chloroform destruction in oxidative conditions.

    Science.gov (United States)

    Kamgang-Youbi, Georges; Poizot, Karine; Lemont, Florent

    2013-01-15

    The performance of a plasma reactor for the degradation of chlorinated hydrocarbon waste is reported. Chloroform was used as a target for a recently patented destruction process based using an inductive plasma torch. Liquid waste was directly injected axially into the argon plasma with a supplied power of ~4kW in the presence of oxygen as oxidant and carrier gas. Decomposition was performed at CHCl(3) feed rates up to 400 g h(-1) with different oxygen/waste molar ratios, chloroform destruction was obtained with at least 99% efficiency and the energy efficiency reached 100 g kWh(-1). The conversion end products were identified and assayed by online FTIR spectroscopy (CO(2), HCl and H(2)O) and redox titration (Cl(2)). Considering phosgene as representative of toxic compounds, only very small quantities of toxics were released (mineral salts, hence, only CO(2) and H(2)O have been found in the final off-gases composition.

  18. Nutrient Recovery of Starch Processing Waste to Cordyceps militaris: Solid State Cultivation and Submerged Liquid Cultivation.

    Science.gov (United States)

    Lee, Joonyeob; Cho, Kyungjin; Shin, Seung Gu; Bae, Hyokwan; Koo, Taewoan; Han, Gyuseong; Hwang, Seokhwan

    2016-09-01

    This study demonstrated the potential for managing starch processing waste (SPW) by bioconversion to Cordyceps militaris mycelia using solid state cultivation (SSC) and submerged liquid cultivation (SLC). The growth characteristics of C. militaris mycelium were accessed and compared for SSC and SLC systems on SPW under various conditions of initial SPW concentration, pH, and operating temperature. To quantify the mycelial biomass in SLC, original primer sets targeting the 18S rRNA gene of C. militaris were developed. In SSC, a maximum mycelial growth rate (543.1 mm(2)/day) was predicted to occur at 25.6 g SPW/L, pH 5.5, and 23.8 °C. In SLC, a maximum mycelial growth rate (1918.6 mg/L/day) was predicted to occur at 35.5 g SPW/L, pH 5.5, and 22.0 °C. Temperature was suggested as the most significant factor in both systems. The higher optimum substrate concentration observed for SLC than for SSC was likely due to difference in mycelial morphology and mixing effect.

  19. Blending municipal solid waste with corn stover for sugar production using ionic liquid process

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Ning [Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Xu, Feng [Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Sandia National Laboratories (SNL-CA), Livermore, CA (United States); Sathitsuksanoh, Noppadon [Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Thompson, Vicki S. [Idaho National Laboratory (INL), Idaho Falls, ID (United States); Cafferty, Kara [Idaho National Laboratory (INL), Idaho Falls, ID (United States); Li, Chenlin [Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Tanjore, Deepti [Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Narani, Akash [Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Pray, Todd R. [Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Simmons, Blake A. [Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Sandia National Laboratories (SNL-CA), Livermore, CA (United States); Singh, Seema [Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States); Sandia National Laboratories (SNL-CA), Livermore, CA (United States)

    2015-06-01

    Municipal solid waste (MSW) represents an attractive cellulosic resource for sustainable fuel production because of its abundance and its low or perhaps negative cost. However, the significant heterogeneity and toxic contaminants are barriers to efficient conversion to ethanol and other products. In this study, we generated MSW paper mix, blended with corn stover (CS), and have shown that both MSW paper mix alone and MSW/CS blends can be efficiently pretreated in certain ionic liquids (ILs) with high yields of fermentable sugars. After pretreatment in 1-ethyl-3-methylimidazolium acetate ([C2C1Im][OAc]), over 80% glucose has been released with enzymatic saccharification. We have also applied an enzyme free process by adding mineral acid and water directly into the IL/biomass slurry to induce hydrolysis. With the acidolysis process in the IL 1-ethyl-3-methylimidazolium chloride ([C2C1Im]Cl), up to 80% glucose and 90% xylose are released for MSW. The results indicate the feasibility of incorporating MSW as a robust blending agent for biorefineries.

  20. A novel dismantling process of waste printed circuit boards using water-soluble ionic liquid.

    Science.gov (United States)

    Zeng, Xianlai; Li, Jinhui; Xie, Henghua; Liu, Lili

    2013-10-01

    Recycling processes for waste printed circuit boards (WPCBs) have been well established in terms of scientific research and field pilots. However, current dismantling procedures for WPCBs have restricted the recycling process, due to their low efficiency and negative impacts on environmental and human health. This work aimed to seek an environmental-friendly dismantling process through heating with water-soluble ionic liquid to separate electronic components and tin solder from two main types of WPCBs-cathode ray tubes and computer mainframes. The work systematically investigates the influence factors, heating mechanism, and optimal parameters for opening solder connections on WPCBs during the dismantling process, and addresses its environmental performance and economic assessment. The results obtained demonstrate that the optimal temperature, retention time, and turbulence resulting from impeller rotation during the dismantling process, were 250 °C, 12 min, and 45 rpm, respectively. Nearly 90% of the electronic components were separated from the WPCBs under the optimal experimental conditions. This novel process offers the possibility of large industrial-scale operations for separating electronic components and recovering tin solder, and for a more efficient and environmentally sound process for WPCBs recycling.

  1. Reduction of 68Ge activity containing liquid waste from 68Ga PET chemistry in nuclear medicine and radiopharmacy by solidification

    NARCIS (Netherlands)

    E. de Blois (Erik); H.S. Chan; K. Roy (Kamalika); E.P. Krenning (Eric); W.A.P. Breeman (Wouter)

    2011-01-01

    textabstractPET with68Ga from the TiO2- or SnO2- based68Ge/68Ga generators is of increasing interest for PET imaging in nuclear medicine. In general, radionuclidic purity (68Ge vs.68Ga activity) of the eluate of these generators varies between 0.01 and 0.001%. Liquid waste containing low amounts of6

  2. Multi-function waste tank facility path forward engineering analysis technical task 3.3, single-shell tank liquid contents

    Energy Technology Data Exchange (ETDEWEB)

    Brown, R.G.; Mattichak, R.W.

    1995-04-28

    Results are reported on actions taken to determine the quantity of liquid wastes in the single shell tanks that still need stabilization, and to determine the amount of flush water needed to support the stabilization effort.

  3. Reduction of (68)Ge activity containing liquid waste from (68)Ga PET chemistry in nuclear medicine and radiopharmacy by solidification.

    Science.gov (United States)

    de Blois, Erik; Chan, Ho Sze; Roy, Kamalika; Krenning, Eric P; Breeman, Wouter A P

    PET with (68)Ga from the TiO2- or SnO2- based (68)Ge/(68)Ga generators is of increasing interest for PET imaging in nuclear medicine. In general, radionuclidic purity ((68)Ge vs. (68)Ga activity) of the eluate of these generators varies between 0.01 and 0.001%. Liquid waste containing low amounts of (68)Ge activity is produced by eluting the (68)Ge/(68)Ga generators and residues from PET chemistry. Since clearance level of (68)Ge activity in waste may not exceed 10 Bq/g, as stated by European Directive 96/29/EURATOM, our purpose was to reduce (68)Ge activity in solution from >10 kBq/g to waste. Most efficient method to reduce the (68)Ge activity is by sorption of TiO2 or Fe2O3 and subsequent centrifugation. The required 10 Bq per mL level of (68)Ge activity in waste was reached by Fe2O3 logarithmically, whereas with TiO2 asymptotically. The procedure with Fe2O3 eliminates ≥90% of the (68)Ge activity per treatment. Eventually, to simplify the processing a recirculation system was used to investigate (68)Ge activity sorption on TiO2, Fe2O3 or Zeolite. Zeolite was introduced for its high sorption at low pH, therefore (68)Ge activity containing waste could directly be used without further interventions. (68)Ge activity containing liquid waste at different HCl concentrations (0.05-1.0 M HCl), was recirculated at 1 mL/min. With Zeolite in the recirculation system, (68)Ge activity showed highest sorption.

  4. Recovery of Metallic Values from Brass Waste Using Brønsted Acidic Ionic Liquid as Leachate

    Science.gov (United States)

    Kilicarslan, Ayfer; Saridede, Muhlis Nezihi

    2015-11-01

    The waste formed during industrial brass manufacturing is rich in copper and zinc metals. Therefore, treatment of this waste is a necessity from economic and environmental aspects. This study presents a process for recovery of zinc and copper through Brønsted ionic liquid (1-butyl-3-methyl-imidazolium hydrogen sulfate; [Bmim]HSO4), as leachate. It was found that all zinc content could be dissolved from the waste under two optimum conditions: (1) in ionic liquid (IL) concentration of 70% (v/v) at 60°C in 30 min or (2) in IL concentration of 50% (v/v) at 100°C in 60 min. On the other hand, ionic liquid leaching gave poor copper solubility under the conditions of the study. Zinc dissolution in the range 5-75 min by [Bmim]HSO4 can be explained with the shrinking core model controlled by diffusion through a product layer, and the apparent activation energy was calculated as 4.36 kJ/mol. The leach liquor was treated to obtain metallic zinc by the electrowinning method without a purification step. Scanning electron microscopy/energy dispersive x-ray spectroscopy (SEM/EDX) investigations showed that the layer of metallic zinc was plated successfully on the cathode.

  5. Durability of class C fly ash belite cement in simulated sodium chloride radioactive liquid waste: Influence of temperature

    Energy Technology Data Exchange (ETDEWEB)

    Guerrero, A. [Eduardo Torroja Institute for Construction Science (CSIC), C/Serrano Galvache 4, 28033 Madrid (Spain)], E-mail: aguerrero@ietcc.csic.es; Goni, S. [Eduardo Torroja Institute for Construction Science (CSIC), C/Serrano Galvache 4, 28033 Madrid (Spain)], E-mail: sgoni@ietcc.csic.es; Allegro, V.R. [Eduardo Torroja Institute for Construction Science (CSIC), C/Serrano Galvache 4, 28033 Madrid (Spain)], E-mail: allegro@ietcc.csic.es

    2009-03-15

    This work is a continuation of a previous durability study of class C fly ash belite cement (FABC-2-W) in simulated radioactive liquid waste (SRLW) that is very rich in sulphate salts. The same experimental methodology was applied in the present case, but with a SRLW rich in sodium chloride. The study was carried out by testing the flexural strength of mortars immersed in simulated radioactive liquid waste that was rich in chloride (0.5 M), and demineralised water as a reference, at 20 and 40 deg. C over a period of 180 days. The reaction mechanism of chloride ions with the mortar was evaluated by scanning electron microscopy (SEM), porosity and pore-size distribution, and X-ray diffraction (XRD). The results showed that the FABC mortar was stable against simulated chloride radioactive liquid waste (SCRLW) attack at the two chosen temperatures. The enhancement of mechanical properties was a result of the formation of non-expansive Friedel's salt inside the pores; accordingly, the microstructure was refined.

  6. DECREASEMENT OF COLOUR AND COD CONTENT OF THE LIQUID WASTE PRODUCT FROM THE JEANS WASHING INDUSTRY BY CHITOSAN AND Trametes versicolor

    OpenAIRE

    Bulan, Rumondang; Sinaga, Mersi Suryani; Darnianti, Darnianti

    2010-01-01

    Chitosan and Trametes versicolor were used as the material for processing liquid waste product from the jeans washing industry in this study as they were more economics and no negative damage in the environmental life. This research is to find out the chitosan and Trametes versicolor effect as the coagulant in decreasing the colour and the COD content of the liquid waste product from the jeans washing industry using the coagulation method and floculation. The dosage of chitosan and Trametes v...

  7. DNA hosted and aligned in aqueous interstitia of a lamellar liquid crystal – a membrane–biomacromolecule interaction model system

    KAUST Repository

    Carlsson, Nils

    2013-01-01

    We report that DNA molecules can be intercalated and macroscopically oriented in the aqueous interstitia of a lyotropic lamellar liquid crystal. Using UV-vis linear dichroism and fluorescence spectroscopy we show that double-stranded oligonucleotides (25 base pairs) in the water-octanoate-decanol system remain base-paired in the B conformation and are confined in two dimensions, with the helix axis preferentially parallel to the lipid bilayer surfaces but free to rotate within this plane. The degree of helix confinement and the corresponding 2-D orientation can be improved by decreasing the thickness of the water interstitia via the fraction of water in the ternary mixture. Not surprisingly, the corresponding single-stranded oligonucleotides are not aligned, with their persistence length being short in comparison to the lamellar interstitium thickness. We propose this as a model system for studying interactions of DNA-ligand complexes near a lipid bilayer membrane which we demonstrate by using dye probes that are either covalently attached to one end of the oligonucleotide or reversibly bound by intercalation between the base pairs. Three cationic dyes, all strongly bound by intercalation to DNA when free in solution, are found to not bind to DNA but to prefer the membrane surface. The covalently attached Cy5 also binds to the bilayer while Cy3 tends to end-stack to the oligonucleotide duplex. The orientation of Cy5 parallel to the membrane indicates that electrostatic surface binding predominates over insertion into the hydrophobic interior of the membrane. Anionic and zwitterionic dyes (FAM and ROX) are found to remain randomly oriented in the water between the lipid bilayer surfaces. © The Royal Society of Chemistry.

  8. Mechanisms of Copper Corrosion in Aqueous Environments. A report from the Swedish National Council for Nuclear Waste's scientific workshop, on November 16, 2009

    Energy Technology Data Exchange (ETDEWEB)

    2010-07-01

    In 2010 the Swedish Nuclear Fuel and Waste Management Company, SKB, plans to submit its license application for the final repository of spent nuclear fuel. The proposed method is the so-called KBS-3 method and implies placing the spent nuclear fuel in copper canisters, surrounded by a buffer of bentonite clay, at 500 m depth in the bedrock. The site selected by SKB to host the repository is located in the municipality of Oesthammar on the Swedish east coast. The copper canister plays a key role in the design of the repository for spent nuclear fuel in Sweden. The long-term physical and chemical stability of copper in aqueous environments is fundamental for the safety evolution of the proposed disposal concept. However, the corrosion resistance of copper has been questioned by results obtained under anoxic conditions in aqueous solution. These observations caused some head-lines in the Swedish newspapers as well as public and political concerns. Consequently, the Swedish National Council for Nuclear Waste organized a scientific workshop on the issue 'Mechanisms of Copper Corrosion in Aqueous Environments'. The purpose of the workshop was to address the fundamental understanding of the corrosion characteristics of copper regarding oxygen-free environments, and to identify what additional information is needed to assess the validity of the proposed corrosion mechanism and its implication on the containment of spent nuclear fuel in a copper canister. This seminar report is based on the presentations and discussions at the workshop. It also includes written statements by the members of the expert panel

  9. Adsorption of Reactive Red 198 Azo Dye fromAqueous Solution onto theWaste Coagulation Sludge of theWater Treatment Plants

    Directory of Open Access Journals (Sweden)

    M. Mahmoudi

    2010-04-01

    Full Text Available "n "n "nBackgrounds and Objectives:Much attention has been recently paid on using waste materials as adsorbents for removal of contaminants from water and wastewater. A new low cost waste was examined for its capacity to adsorb RR198, an azo reactive model dye, from an aqueous solution."nMaterials andMethods: The waste was dried, powdered and characterized before being used as an adsorbent. The effects of pH (3-10, adsorbent dose (0.2-3 g, dye concentration and contact time on the adsorption efficiency were investigated. Equilibrium study data were modeled using Langmuir and Freundlich models."nResults: The characterization analysis indicated that itwas composedmainly of ferric hydroxide. The powder had a BET and average pore size of 107 m2/g and 4.5 nm, respectively. The results showed that dye removal was highest at a solution pH of 7 to 8 and a powder dose of 2 g/L. The RR198 removal percentage decreased from 100& to 43& at 140 min contact time when the concentration of dye was increased from 25 mg/L to 100 mg/L, at optimum pH and dosage. The Langmuir equation provided the best fit for the experimental data. The maximum adsorption capacity was calculated to be 34.4 mg/g."nConclusion: According to the obtained results, the water coagulation waste sludge appears to be a suitable low cost and effcient adsorbent for removing reactive azo dyes from waste streams.

  10. Treatment of liquid wastes generated by maintenance operations applied to motor vehicles; Tratamiento de residuos liquidos generados en las operaciones de mantenimiento de vehiculos a motor

    Energy Technology Data Exchange (ETDEWEB)

    Lloret i Bosca, G.; Boch Mossi, F.; Oyonarte Andres, S.; Colomer Signes, S.; Soro Casanova, J. R.

    2007-07-01

    The Life European project Urban-Bat presents an innovating approach to liquid wastes generated by maintenance operations applied to bus fleets by defining, through implementation of Best Available Technologies (Bat), a waste management model based on reduction of environmental impact and on life span increase of raw materials. This will take place at the very point of generation thus minimizing the need for an external waste management. (Author) 5 refs.

  11. The main rules regarding the management of solid waste and liquid effluent contaminated during use at nuclear medicine departments; Les principales regles de gestion des dechets solides et des effluents liquides contamines dans les services de medecine nucleaire

    Energy Technology Data Exchange (ETDEWEB)

    Boudouin, E. [Autorite de Surete Nucleaire, Direction des rayonnements ionisants et de la sante, 75 - Paris (France)

    2011-02-15

    This article describes the key requirements applicable to the management of contaminated medical waste and effluent from hospitals and health care centres, and more especially from nuclear medicine departments that use radionuclides for the purposes of diagnosis (in vivo or in vitro) or in patient treatment. It also presents the key management regulations, making a distinction between contaminated solid waste and contaminated liquid waste from such nuclear medicine departments. (author)

  12. Use of Novel Highly Selective Ion Exchange Media for Minimizing the Waste Arising from Different NPP and Other Liquids

    Energy Technology Data Exchange (ETDEWEB)

    Tusa, Esko; Harjula, Risto; Lehto, Jukka

    2003-02-25

    Highly selective inorganic ion exchangers give new possibilities to implement and operate new innovative treatment systems for radioactive liquids. Because of high selectivity these ion exchangers can be used even in liquids of high salt concentrations. Only selected target nuclides will be separated and inactive salts are left in the liquid, which can be released or recategorized. Thus, it is possible to reduce the volume of radioactive waste dramatically. On the other hand, only a small volume of highly selective material is required in applications, which makes it possible to design totally new types of compact treatment systems. The major benefit of selective ion exchange media comes from the very large volume reduction of radioactive waste in final disposal. It is also possible to save in investment costs, because small ion exchanger volumes can be used and handled in a very small facility. This paper describes different applications of these highly selective ion exchangers, both commercial fullscale applications and laboratory tests, to give the idea of their efficiency for different liquids.

  13. [Distribution and activity of microorganisms in the deep repository for liquid radioactive waste at the Siberian Chemical Combine].

    Science.gov (United States)

    Nazina, T N; Luk'ianova, E A; Zakharova, E V; Ivoĭlov, V S; Poltaraus, A B; Kalmykov, S N; Beliaev, S S; Zubkov, A A

    2006-01-01

    The physicochemical conditions, composition of microbial communities, and the rates of anaerobic processes in the deep sandy horizons used as a repository for liquid radioactive wastes (LRW) at the Siberian Chemical Combine (Seversk, Tomsk oblast), were studied. Formation waters from the observation wells drilled into the production horizons of the radioactive waste disposal site were found to be inhabited by microorganisms of different physiological groups, including aerobic organotrophs, anaerobic fermentative, denitrifying, sulfate-reducing, and methanogenic bacteria. The density of microbial population, as determined by cultural methods, was low and usually did not exceed 10(4) cells/ml. Enrichment cultures of microorganisms producing gases (hydrogen, methane, carbon dioxide, and hydrogen sulfide) and capable of participation in the precipitation of metal sulfides were obtained from the waters of production horizons. The contemporary processes of sulfate reduction and methanogenesis were assayed; the rates of these terminal processes of organic matter destruction were found to be low. The denitrifying bacteria from the underground repository were capable of reducing the nitrates contained in the wastes, provided sources of energy and biogenic elements were available. Biosorption of radionuclides by the biomass of aerobic bacteria isolated from groundwater was demonstrated. The results obtained give us insight into the functional structure of the microbial community inhabiting the waters of repository production horizons. This study indicates that the numbers and activity of microbial cells are low both inside and outside the zone of radioactive waste dispersion, in spite of the long period of waste discharge.

  14. Occurrence mode and concentration of chlorine in liquid product from co-pyrolysis of waste plastic and coal

    Energy Technology Data Exchange (ETDEWEB)

    Li Zhen; Liu Ze-chang; Zhou Li-xia [Chemical and Environmental Department of Taishan College, Taian (China)

    2009-08-15

    The occurrence mode and concentration of chlorine in liquid product including tar and water from co-pyrolysis of waste plastic (WP) and coal were studied. The effect of temperature, holding time, heating rate and gas flow on chlorine concentration in the liquid product was examined. The result indicates that the addition of WP to coal in co-pyrolysis does not increase the organic chlorine compound in the liquid product. However, the tar yield increases, and the water yield decreases. The chlorine in water mainly exists as inorganic form (NH{sub 4}Cl) and organic amine hydrochloride. There is no obvious C-Cl band in IR spectra of tar is observed. This indicates that the organic chlorine in tar is very little. 10 refs., 6 figs., 2 tabs.

  15. Deoxygenation of waste cooking oil and non-edible oil for the production of liquid hydrocarbon biofuels.

    Science.gov (United States)

    Romero, M J A; Pizzi, A; Toscano, G; Busca, G; Bosio, B; Arato, E

    2016-01-01

    Deoxygenation of waste cooking vegetable oil and Jatropha curcas oil under nitrogen atmosphere was performed in batch and semi-batch experiments using CaO and treated hydrotalcite (MG70) as catalysts at 400 °C. In batch conditions a single liquid fraction (with yields greater than 80 wt.%) was produced containing a high proportion of hydrocarbons (83%). In semi-batch conditions two liquid fractions (separated by a distillation step) were obtained: a light fraction and an intermediate fraction containing amounts of hydrocarbons between 72-80% and 85-88% respectively. In order to assess the possible use of the liquid products as alternative fuels a complete chemical characterization and measurement of their properties were carried out.

  16. PLUTONIUM FINISHING PLANT (PFP) 241-Z LIQUID WASTE TREATMENT FACILITY DEACTIVATION AND DEMOLITION

    Energy Technology Data Exchange (ETDEWEB)

    JOHNSTON GA

    2008-01-15

    Fluor Hanford, Inc. (FH) is proud to submit the Plutonium Finishing Plant (PFP) 241-Z liquid Waste Treatment Facility Deactivation and Demolition (D&D) Project for consideration by the Project Management Institute as Project of the Year for 2008. The decommissioning of the 241-Z Facility presented numerous challenges, many of which were unique with in the Department of Energy (DOE) Complex. The majority of the project budget and schedule was allocated for cleaning out five below-grade tank vaults. These highly contaminated, confined spaces also presented significant industrial safety hazards that presented some of the most hazardous work environments on the Hanford Site. The 241-Z D&D Project encompassed diverse tasks: cleaning out and stabilizing five below-grade tank vaults (also called cells), manually size-reducing and removing over three tons of process piping from the vaults, permanently isolating service utilities, removing a large contaminated chemical supply tank, stabilizing and removing plutonium-contaminated ventilation ducts, demolishing three structures to grade, and installing an environmental barrier on the demolition site . All of this work was performed safely, on schedule, and under budget. During the deactivation phase of the project between November 2005 and February 2007, workers entered the highly contaminated confined-space tank vaults 428 times. Each entry (or 'dive') involved an average of three workers, thus equaling approximately 1,300 individual confined -space entries. Over the course of the entire deactivation and demolition period, there were no recordable injuries and only one minor reportable skin contamination. The 241-Z D&D Project was decommissioned under the provisions of the 'Hanford Federal Facility Agreement and Consent Order' (the Tri-Party Agreement or TPA), the 'Resource Conservation and Recovery Act of 1976' (RCRA), and the 'Comprehensive Environmental Response, Compensation, and

  17. A critical assessment of the mechanisms governing the formation of aqueous biphasic systems composed of protic ionic liquids and polyethylene glycol†

    Science.gov (United States)

    Cláudio, Ana Filipa M.; Pereira, Jorge F. B.; McCrary, Parker D.; Freire, Mara G.; Coutinho, João A. P.; Rogers, Robin D.

    2017-01-01

    An extensive study on the formation of aqueous biphasic systems (ABS) using aqueous solutions of protic ionic liquids (PILs) and polyethylene glycol (PEG) was performed in order to understand the mechanisms underlying the phase separation. Aqueous solutions of PEG polymers with different molecular weights (600, 1000, 2000, and 3400 g mol−1) and several N-alkyl-, dialkyl-, and trialkyl-ammonium salts of acetate, propanoate, butanoate, hexanoate and octanoate were prepared and their ability to form ABS at several temperatures assessed. The ternary liquid–liquid phase diagrams were determined at several temperatures, as well as binary PIL (or salt)-PEG-1000 and salt-water solubility data to better clarify the mechanisms responsible for the phase separation. All data gathered indicate that the formation of PEG–PIL-based ABS is mainly governed by the PIL–PEG mutual interactions, where PILs with a higher solubility in the polymer exhibit a lower aptitude to form ABS displaying thus a smaller biphasic region, for which a direct correlation was identified. The effects of the molecular weight and temperature of the polymer were also addressed. The increase of the PEG hydrophobicity or molecular weight favours the phase separation, whereas the effect of temperature was found to be more complex and dependent on the nature of the PIL, with an increase or decrease of the biphasic regime with an increase in temperature. PMID:27774550

  18. Lyotropic, liquid crystalline nanostructures of aqueous dilutions of SMEDDS revealed by small-angle X-ray scattering: impact on solubility and drug release.

    Science.gov (United States)

    Goddeeris, Caroline; Goderis, Bart; Van den Mooter, Guy

    2010-05-12

    The present study was conducted to characterise the liquid crystalline phases that occur upon diluting a SMEDDS and to elucidate the role of these phases on drug solubilisation and release. Small-angle X-ray scattering (SAXS) was used to probe the structures in aqueous dilutions of 3 SMEDDS consisting of propylene glycol mono- and dicaprylate and mono- and dicaprate (PGDCDC) and d-alpha-tocopheryl polyethylene glycol succinate 1000 (TPGS 1000), polysorbate 80 (P80) or polyoxyl 40 hydrogenated castor oil (P40HC). The scattering patterns revealed the formation of either a random periodic or a lamellar phase when 10% (w/w) water was added. All formulations exhibited lamellar structures at 20% (w/w) aqueous dilution, of which the layer-to-layer distance increased upon further addition of water. At 40% (w/w) water, a hexagonal or lamellar phase was formed, depending on the geometry of the surfactant. Temperature did not alter the phases formed. Incorporation of the drug UC 781 only slightly enlarged the characteristic dimensions of the liquid crystalline phases. Drug solubility decreased upon aqueous dilution, although 10% (w/w) dilutions of PGDCDC-P80 SMEDDS and PGDCDC-TPGS 1000 SMEDDS revealed a highly increased solubility as compared to the pure formulations. Drug release data revealed that UC 781 release could not be linked to the solubilisation capacity of the SMEDDS, but could be associated with the solubility of UC 781 in the phases formed at water concentrations above 10% (w/w).

  19. In Situ Dissimilatory Nitrate Reduction to Ammonium in a Paddy Soil Fertilized with Liquid Cattle Waste

    Institute of Scientific and Technical Information of China (English)

    LU Wei-Wei; S.RIYA; ZHOU Sheng; M.HOSOMI; ZHANG Hai-Lin; SHI Wei-Ming

    2012-01-01

    Most studies on dissimilatory nitrate reduction to ammonium (DNRA) in paddy soils were conducted in the laboratory and in situ studies are in need for better understanding of the DNRA process.In this study,in situ incubations of soil DNRA using 15N tracer were carried out in paddy fields under conventional water (CW) and low water (LW) managements to explore the potential of soil DNRA after liquid cattle waste (LCW) application and to investigate the impacts of soil redox potential (Eh) and labile carbon on DNRA.DNRA rates ranged from 3.06 to 10.40 mg N kg -1 dry soil d-1,which accounted for 8.55%-12.36% and 3.88%-25.44% of consunption of added NO3-15N when Eh at 5 cm soil depth ranged from 230 to 414 mV and -225 to -65 mV,respectively.DNRA rates showed no significant difference in paddy soils under two water managements although soil Eh and/or dissolved organic carbon (DOC) were more favorable for DNRA in the paddy soil under CW management 1 d before,or 5 and 7 d after LCW application.Soil DNRA rates were negatively correlated with soil Eh (P < 0.05,n =5) but positively correlated with soil DOC (P < 0.05,n =5) in the paddy soil under LW management,while no significant correlations were shown in the paddy soil under CW management.The potential of DNRA measured in situ was consistent with previous laboratory studies; and the controlling factors of DNRA in paddy soils might be different under different water managements,probably due to the presence of different microfloras of DNRA.

  20. THE ROLE OF LIQUID WASTE PRETREATMENT TECHNOLOGIES IN SOLVING THE DOE CLEAN-UP MISSION

    Energy Technology Data Exchange (ETDEWEB)

    Wilmarth, B; Sheryl Bush, S

    2008-10-31

    The objective of this report is to describe the pretreatment solutions that allow treatment to be tailored to specific wastes, processing ahead of the completion schedules for the main treatment facilities, and reduction of technical risks associated with future processing schedules. Wastes stored at Hanford and Savannah River offer challenging scientific and engineering tasks. At both sites, space limitations confound the ability to effectively retrieve and treat the wastes. Additionally, the radiation dose to the worker operating and maintaining the radiochemical plants has a large role in establishing the desired radioactivity removal. However, the regulatory requirements to treat supernatant and saltcake tank wastes differ at the two sites. Hanford must treat and remove radioactivity from the tanks based on the TriParty Agreement and Waste Incidental to Reprocessing (WIR) documentation. These authorizing documents do not specify treatment technologies; rather, they specify endstate conditions. Dissimilarly, Waste Determinations prepared at SRS in accordance with Section 3116 of the 2005 National Defense Authorization Act along with state operating permits establish the methodology and amounts of radioactivity that must be removed and may be disposed of in South Carolina. After removal of entrained solids and site-specific radionuclides, supernatant and saltcake wastes are considered to be low activity waste (LAW) and are immobilized in glass and disposed of at the Hanford Site Integrated Disposal Facility (IDF) or formulated into a grout for disposal at the Savannah River Site Saltstone Disposal Facility. Wastes stored at the Hanford Site or SRS comprise saltcake, supernate, and sludges. The supernatant and saltcake waste fractions contain primarily sodium salts, metals (e.g., Al, Cr), cesium-137 (Cs-13