WorldWideScience

Sample records for aqueous salt systems

  1. Ionic Liquid-salt Aqueous Two-phase System, a Novel System for the Extraction of Abused Drugs

    Institute of Scientific and Technical Information of China (English)

    She Hong LI; Chi Yang HE; Hu Wei LIU; Ke An LI; Feng LIU

    2005-01-01

    A 1-butyl-3-methylimidazolium chloride-salt aqueous two-phase system was studied on extraction of abused drugs. The effects of sorts of salts, temperature, concentration of salt and drugs on system were investigated systematically. A satisfactory extraction efficiency of 93%was obtained for papaverine while that of morphine was 65%. The extraction mechanism was primarily discussed.

  2. Ionic liquid-salt based aqueous biphasic system separation of 109Cd from silver target

    International Nuclear Information System (INIS)

    The Aqueous Biphasic Systems (ABS) is becoming more important from green chemistry point of view replacing conventional liquid-liquid extraction system. The most of the aqueous biphasic systems reported in the literature are based on Polyethylene glycol (PEG) with different salts. Although ABS based on water soluble room temperature ionic liquid (RTIL) 1-butyl-3-methylimidazolium Chloride ((bmim)CI) and concentrated solutions of kosmotropic salt K2HPO4 was reported in 2007 but the efficiency of this system for metal partitioning has been rarely explored. We report for the first time separation of no-carrier-added (NCA) 109Cd from the α-particle irradiated Ag target using this ABS

  3. Secondary Confinement of Water Observed in Eutectic Melting of Aqueous Salt Systems in Nanopores.

    Science.gov (United States)

    Meissner, Jens; Prause, Albert; Findenegg, Gerhard H

    2016-05-19

    Freezing and melting of aqueous solutions of alkali halides confined in the cylindrical nanopores of MCM-41 and SBA-15 silica was probed by differential scanning calorimetry (DSC). We find that the confinement-induced shift of the eutectic temperature in the pores can be significantly greater than the shift of the melting temperature of pure water. Greatest shifts of the eutectic temperature are found for salts that crystallize as oligohydrates at the eutectic point. This behavior is explained by the larger fraction of pore volume occupied by salt hydrates as compared to anhydrous salts, on the assumption that precipitated salt constitutes an additional confinement for ice/water in the pores. A model based on this secondary confinement effect gives a good representation of the experimental data. Salt-specific secondary confinement may play a role in a variety of fields, from salt-impregnated advanced adsorbents and catalysts to the thermal weathering of building materials. PMID:27124392

  4. Thermodynamic modelling of phase equilibrium for water + poly(Ethylene glycol + salt aqueous two-phase systems

    Directory of Open Access Journals (Sweden)

    R.A.G. Sé

    2002-04-01

    Full Text Available The NRTL (nonrandom, two-liquid model, expressed in mass fraction instead of mole fraction, was used to correlate liquid-liquid equilibria for aqueous two-phase polymer-salt solutions. New interaction energy parameters for this model were determined using reported data on the water + poly(ethylene glycol + salt systems, with different molecular masses for PEG and the salts potassium phosphate, sodium sulfate, sodium carbonate and magnesium sulfate. The correlation of liquid-liquid equilibrium is quite satisfactory.

  5. Phase Diagrams of the Aqueous Two-Phase Systems of Poly(ethylene glycol)/Sodium Polyacrylate/Salts

    OpenAIRE

    Adalberto Pessoa Junior; Hans-Olof Johansson; Eloi Feitosa

    2011-01-01

    Aqueous two-phase systems consisting of polyethylene glycol (PEG), sodium polyacrylate (NaPAA), and a salt have been studied. The effects of the polymer size, salt type (NaCl, Na2SO4, sodium adipate and sodium azelate) and salt concentrations on the position of the binodal curve were investigated. The investigated PEG molecules had a molar mass of 2,000 to 8,000 g/mol, while that of NaPAA was 8,000 g/mol. Experimental phase diagrams, and tie lines and calculated phase diagrams, based on Flory...

  6. Extraction of amylase from fermentation broth in poly (Ethylene Glycol salt aqueous two-phase system

    Directory of Open Access Journals (Sweden)

    Raquel Pedrosa Bezerra

    2006-07-01

    Full Text Available Studies were carried out on the partition of amylase from Bacillus subtilis in a minimal medium at 37 ºC and 110 rpm. Enzyme recovery was carried out in aqueous two-phase system PEG-Phosphate salt were carried out. The best purification factor (5.4 was obtained in system PEG 1000 (16.7% w/w with potassium phosphate (14.8% w/w, at pH 6.0, resulting in a recovery of 45.2% activity enzymatic in the salt-rich phase.Enzimas amilolíticas têm sido amplamente investigadas com a finalidade de melhorar os processos industriais para a degradação do amido. Foi determinado que a extração da enzima em sistema bifásico aquosos é um método aplicável para separação e purificação de biomoléculas em misturas. Vários sistemas compostos de soluções aquosas de polietilenoglicol e fosfato foram avaliados. Estudos de produção em meio mínimo suplementado, à 37ºC, com uma velocidade de agitação de 110rpm e recuperação da amilase a partir do Bacillus subtilis em sistema bifásico aquoso PEG-fosfato foram avaliados. O melhor fator de purificação (5.4 foi obtido no sistema PEG 1000 (16.7% w/w com fosfato de potássio (14.8% w/w, a pH 6.0, resultando na recuperação da atividade enzimática de 45.2% na fase rica em sal.

  7. Phase Diagrams of the Aqueous Two-Phase Systems of Poly(ethylene glycol/Sodium Polyacrylate/Salts

    Directory of Open Access Journals (Sweden)

    Adalberto Pessoa Junior

    2011-03-01

    Full Text Available Aqueous two-phase systems consisting of polyethylene glycol (PEG, sodium polyacrylate (NaPAA, and a salt have been studied. The effects of the polymer size, salt type (NaCl, Na2SO4, sodium adipate and sodium azelate and salt concentrations on the position of the binodal curve were investigated. The investigated PEG molecules had a molar mass of 2,000 to 8,000 g/mol, while that of NaPAA was 8,000 g/mol. Experimental phase diagrams, and tie lines and calculated phase diagrams, based on Flory-Huggins theory of polymer solutions are presented. Due to strong enthalpic and entropic balancing forces, the hydrophobicity of the added salt has a strong influence on the position of the binodal, which could be reproduced by model calculations.

  8. Liquid-Liquid Equilibria of Aqueous Two-phase Systems Containing Polyethylene Glycol 4000 and Two Different Salts of Ammonium

    Directory of Open Access Journals (Sweden)

    G. Khayati

    2011-02-01

    Full Text Available The aim of this study was to survey on phase diagrams and Liquid-Liquid Equilibrium (LLE data of the aqueous PEG4000 - (NH42HPO4 and PEG4000 - (NH42SO4 systems experimentally at 298.15 K. The salting-out effect was also discussed on the basis of the Gibbs free energy of hydration of ions. The experimental binodal data were satisfactorily correlated with the Merchuk equation. Tie line compositions were correlated using the Othmer-Tobias and Bancroft equations, and the parameters have also reported. Good agreement was obtained with the experimental data with the model equations.

  9. Partitioning of L-methionine in aqueous two-phase systems containing poly(propylene glycol) and sodium phosphate salts

    Energy Technology Data Exchange (ETDEWEB)

    Salabat, Alireza, E-mail: a-salabat@araku.ac.ir [Chemistry Department, Arak University, P.O. Box 38156-879, Arak (Iran, Islamic Republic of); Sadeghi, Rahmat [Department of Chemistry, University of Kurdistan, Sanandaj, Kurdistan 66135 (Iran, Islamic Republic of); Moghadam, Somayeh Tiani [Chemistry Department, Arak University, P.O. Box 38156-879, Arak (Iran, Islamic Republic of); Jamehbozorg, Bahman [Department of Chemistry, University of Kurdistan, Sanandaj, Kurdistan 66135 (Iran, Islamic Republic of)

    2011-10-15

    Highlights: > Thermodynamics parameters for partitioning of L-methionine in ATPS. > Investigation of different effects on partition coefficient of the amino acid. > Propose the best condition for L-methionine partitioning. - Abstract: The partitioning behavior of L-methionine has been studied in aqueous two-phase systems of (poly(propylene glycol) + sodium phosphate salts + H{sub 2}O) at different temperatures. The salts used were sodium di-hydrogen phosphate (NaH{sub 2}PO{sub 4}), di-sodium hydrogen phosphate (Na{sub 2}HPO{sub 4}) and tri-sodium phosphate (Na{sub 3}PO{sub 4}). The effects of tie line length, salt type, and temperature on the partition coefficient of this amino acid have been studied. In addition, thermodynamic parameters ({Delta}H{sup o}, {Delta}S{sup o} and {Delta}G{sup o}) as a function of temperature were calculated. The results showed that increasing tie line length led to decreasing of the partition coefficient. We also showed that the partition coefficients of the amino acid in the systems containing Na{sub 3}PO{sub 4} are greater than the other two salts. Moreover, it is verified that increasing temperature led to decreasing the partition coefficient. The experimental partition coefficient data are correlated using a modified virial-type model.

  10. Aqueous salt blanket tritium systems for the TITAN-II reversed-field pinch fusion reactor design

    International Nuclear Information System (INIS)

    TITAN is a high-power-density reversed-field pinch reactor design. The TITAN-II concept is based on an aqueous lithium salt blanket immersed in a loop-in-pool design to provide a high level of passive safety. The blanket uses 50 Ci/kg water in the primary heat transport circuit, and 0.4 Ci/kg in the cold water pool. The main coolant stream is treated by a 5-stage Vapor Phase Catalytic Exchange process, followed by Cryogenic Distillation. Water Distillation is used to process the cold pool. The design uses proven technologies (although on a ten times larger scale), and takes advantage of features of light water tritium recovery. Tritium losses are controlled to 50 Ci/d by leak-tight design, tritium release trapping by the cold pool, lower pressure in the primary system relative to the steam system, and air driers

  11. Experimental determination and thermodynamic modeling of phase equilibrium and protein partitioning in aqueous two-phase systems containing biodegradable salts

    International Nuclear Information System (INIS)

    Highlights: ► Binodal data of systems (water + polyethyleneglycol + sodium) succinate are reported. ► Pitzer model describes the phase equilibrium of systems formed by polyethyleneglycol and biodegradable salts satisfactorily. ► This simple thermodynamic framework was able to predict the partitioning behaviour of model proteins acceptably well. - Abstract: Phase diagrams of sustainable aqueous two-phase systems (ATPSs) formed by polyethyleneglycols (PEGs) of different average molar masses (4000, 6000, and 8000) and sodium succinate are reported in this work. Partition coefficients (Kps) of seven model proteins: bovine serum albumin, catalase, beta-lactoglobulin, alpha-amylase, lysozyme, pepsin, urease and trypsin were experimentally determined in these systems and in ATPSs formed by the former PEGs and other biodegradable sodium salts: citrate and tartrate. An extension of Pitzer model comprising long and short-range term contributions to the excess Gibbs free energy was used to describe the (liquid + liquid) equilibrium. Comparison between experimental and calculated tie line data showed mean deviations always lower than 3%, thus indicating a good correlation. The partition coefficients were modeled by using the same thermodynamic approach. Predicted and experimental partition coefficients correlated quite successfully. Mean deviations were found to be lower than the experimental uncertainty for most of the assayed proteins.

  12. Separation of porcine parvovirus from bovine serum albumin using PEG-salt aqueous two-phase system.

    Science.gov (United States)

    Vijayaragavan, K Saagar; Zahid, Amna; Young, Jonathan W; Heldt, Caryn L

    2014-09-15

    Vaccine production faces a challenge in adopting conventional downstream processing steps that can efficiently purify large viral particles. Some major issues that plague vaccine purification are purity, potency, and quality. The industry currently considers 30% as an acceptable virus recovery for a vaccine purification process, including all downstream processes, whereas antibody recovery from CHO cell culture is generally around 80-85%. A platform technology with an improved virus recovery would revolutionize vaccine production. In a quest to fulfill this goal, we have been exploring aqueous two-phase systems (ATPSs) as an optional mechanism to purify virus. ATPS has been unable to gain wide implementation mainly due to loss of virus infectivity, co-purification of proteins, and difficulty of polymer recycling. Non-enveloped viruses are chemically resistant enough to withstand the high polymer and salt concentrations that are required for effective ATPS separations. We used infectious porcine parvovirus (PPV), a non-enveloped, DNA virus as a model virus to test and develop an ATPS separation method. We successfully tackled two of the three main disadvantages of ATPS previously stated; we achieved a high infectious yield of 64% in a PEG-citrate ATPS process while separating out the main contaminate protein, bovine serum albumin (BSA). The most dominant forces in the separation were biomolecule charge, virus surface hydrophobicity, and the ATPS surface tension. Highly hydrophobic viruses are likely to benefit from the discovered ATPS for high-purity vaccine production and ease of implementation. PMID:25086421

  13. Extended UNIQUAC model for correlation and prediction of vapour-liquid-solid equilibria in aqueous salt systems containing non-electrolytes

    DEFF Research Database (Denmark)

    Iliuta, Maria C.; Thomsen, Kaj; Rasmussen, Peter

    2000-01-01

    The Extended UNIQUAC model has previously been used to describe the excess Gibbs energy for aqueous electrolyte mixtures. It is an electrolyte model formed by combining the original UNIQUAC model, the Debye-Huckel law and the Soave-Redlich-Kwong equation of state. In this work the model is extended...... the phase behaviour of methanol-water-three salts systems is illustrated. (C) 2000 Elsevier Science Ltd. All rights reserved....

  14. Preliminary study on lithium-salt aqueous solution blanket

    International Nuclear Information System (INIS)

    Aqueous solution blanket using lithium salts such as LiNO3 and LiOH have been studied in the US-TIBER program and ITER conceptual design activity. In the JAERI/LANL collaboration program for the joint operation of TSTA (Tritium Systems Test Assembly), preliminary design work of blanket tritium system for lithium ceramic blanket, aqueous solution blanket and liquid metal blanket, have been performed to investigate technical feasibility of tritium demonstration tests using the TSTA. Detail study of the aqueous solution blanket concept have not been performed in the Japanese fusion program, so that this study was carried out to investigate features of its concept and to evaluated its technical problems. The following are the major items studied in the present work: (i) Neutronics of tritium breeding ratio and shielding performance Lithium concentration, Li-60 enrichment, beryllium or lead, composition of structural material/beryllium/solution, heavy water, different lithium-salts (ii) Physicochemical properties of salts Solubility, corrosion characteristics and compatibility with structural materials, radiolysis (iii) Estimation of radiolysis in ITER aqueous solution blanket. (author)

  15. Phase Separation Behavior and System Properties of Aqueous Two-Phase Systems with Polyethylene Glycol and Different Salts: Experiment and Correlation

    OpenAIRE

    Haihua Yuan; Yang Liu; Wanqian Wei; Yongjie Zhao

    2015-01-01

    The phase separation behaviors of PEG1000/sodium citrate, PEG4000/sodium citrate, PEG1000/ammonium sulfate, and PEG4000/ammonium sulfate aqueous two-phase systems were investigated, respectively. There are two distinct situations for the phase separation rate in the investigated aqueous two-phase systems: one state is top-continuous phase with slow phase separation rate and strong bottom-continuous phase with fast phase separation rate and weak volume ratio dependence. The system properties s...

  16. Direct Purification of Pectinase from Mango (Mangifera Indica Cv. Chokanan Peel Using a PEG/Salt-Based Aqueous Two Phase System

    Directory of Open Access Journals (Sweden)

    Abdul Manap Mohd Yazid

    2011-10-01

    Full Text Available An Aqueous Two-Phase System (ATPS was employed for the first time for the separation and purification of pectinase from mango (Mangifera Indica Cv. Chokanan peel. The effects of different parameters such as molecular weight of the polymer (polyethylene glycol, 2,000–10,000, potassium phosphate composition (12–20%, w/w, system pH (6–9, and addition of different concentrations of neutral salts (0–8%, w/w on partition behavior of pectinase were investigated. The partition coefficient of the enzyme was decreased by increasing the PEG molecular weight. Additionally, the phase composition showed a significant effect on purification factor and yield of the enzyme. Optimum conditions for purification of pectinase from mango peel were achieved in a 14% PEG 4000-14% potassium phosphate system using 3% (w/w NaCl addition at pH 7.0. Based on this system, the purification factor of pectinase was increased to 13.2 with a high yield of (97.6%. Thus, this study proves that ATPS can be an inexpensive and effective method for partitioning of pectinase from mango peel.

  17. 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. PMID:21168562

  18. Production of γ-cyclodextrin by Bacillus cereus cyclodextrin glycosyltransferase using extractive bioconversion in polymer-salt aqueous two-phase system.

    Science.gov (United States)

    Lin, Yu Kiat; Show, Pau Loke; Yap, Yee Jiun; Ariff, Arbakariya B; Mohammad Annuar, Mohammad Suffian; Lai, Oi Ming; Tang, Teck Kim; Juan, Joon Ching; Ling, Tau Chuan

    2016-06-01

    Aqueous two-phase system (ATPS) extractive bioconversion provides a technique which integrates bioconversion and purification into a single step process. Extractive bioconversion of gamma-cyclodextrin (γ-CD) from soluble starch with cyclodextrin glycosyltransferase (CGTase, EC 2.4.1.19) enzyme derived from Bacillus cereus was evaluated using polyethylene glycol (PEG)/potassium phosphate based on ATPS. The optimum condition was attained in the ATPS constituted of 30.0% (w/w) PEG 3000 g/mol and 7.0% (w/w) potassium phosphate. A γ-CD concentration of 1.60 mg/mL with a 19% concentration ratio was recovered after 1 h bioconversion process. The γ-CD was mainly partitioned to the top phase (YT=81.88%), with CGTase partitioning in the salt-rich bottom phase (KCGTase=0.51). Repetitive batch processes of extractive bioconversion were successfully recycled three times, indicating that this is an environmental friendly and a cost saving technique for γ-CD production and purification. PMID:26702953

  19. Influence of the iodide/iodine redox system on the self-discharge of AC/AC electrochemical capacitors in salt aqueous electrolyte

    Directory of Open Access Journals (Sweden)

    Qamar Abbas

    2015-12-01

    Full Text Available Self-discharge (SD of AC/AC (AC=activated carbon electrochemical capacitors in aqueous solutions of lithium sulfate (Li2SO4 and lithium sulfate+iodide salts (Li2SO4+KI or Li2SO4+LiI was investigated at 24 °C and −40 °C after cell potential hold at values from 1 V to 1.6 V. At 24 °C, the cells exhibit lower SD in Li2SO4+KI than in Li2SO4, owing to the redox activity of the 2I−/I2 system which drives the positive AC electrode to operate in narrow potential range and display lower potential drop than in Li2SO4. At −40°C, the capacitors exhibit comparable and reduced SD both in Li2SO4+LiI and Li2SO4, whatever the holding cell potential. Three-electrode cell experiments demonstrate that, at −40 °C, hydrogen chemisorption is thermodynamically unfavored under negative polarization, while the activity of the 2I−/I2 redox system under positive polarization is only slightly reduced. As a consequence, the AC/AC cells in Li2SO4 exhibit a typical electrical double-layer performance at −40°C, whereas they still behave as hybrid ones in Li2SO4+LiI, with twice higher capacitance than in Li2SO4. The (Ui-Ut vs t1/2 plots demonstrate that SD is essentially controlled by diffusion at −40°C, suggesting that it originates from bulkier hydrated ions. Overall, in the investigated temperature range, the AC/AC capacitors in Li2SO4+LiI demonstrate low self-discharge and high capacitance, while being able to operate up to 1.6 V.

  20. Metal separations using aqueous biphasic partitioning systems

    International Nuclear Information System (INIS)

    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. Radiation-induced reduction of ditetrazolium salt in aqueous solutions

    International Nuclear Information System (INIS)

    Color formation in aqueous solutions of the ditetrazolium salt blue tetrazolium (BT2+) in the absence or presence of oxygen is a complex radiation chemical reaction. The final stable product is the poorly soluble diformazan violet to blue pigment having a broad spectral absorption band (λmax=552 nm). The reaction of BT2+ with the hydrated electron proceeds by rapid reduction of BT2+ followed by protonation at the nitrogen closest to the unsubstituted phenyl group, via the two intermediate tetrazolinyl radicals shared by the ditetrazole ring nitrogens. The effect of solution pH, N2O saturation, and the presence of the reducing agent dextrose are examined. The system serves as a radiochromic sensor and a dosimeter of ionizing radiations. Solutions of 5 mmol l-1 BT2+ at pH 7.3 serve as dosimeters over an absorbed-dose range of approximately 0.2-6 kGy (dearated, with a range of 1-8 mmol l-1 dextrose) and of about 1-15 kGy (aerated, with 0.1 mol l-1 sodium formate and 5 mmol l-1 dextrose)

  2. Cast iron deterioration with time in various aqueous salt solutions

    Indian Academy of Sciences (India)

    Rita Mehra; Aditi Soni

    2002-02-01

    The changes with time in the corrosion rate and corrosion current density on a cast iron electrode in various aqueous salt solutions have been carried out using total immersion test and potentiostatic polarization curves. The concentration of salts taken is expected to be present in potable water. The relative behaviour of these salts towards corrosion has also been studied, which is found to be different from previous studies. The total immersion test parameters viz. weight loss, corrosion rate as well as potentiostatic parameters, open circuit potential, corr, Tafel slopes, corrosion rate, have been calculated by standard methods. Besides these the relative increase in corrosion rate with time as well as the percentage to which corrosion rate should be decreased so as to provide protection towards corrosion have also been calculated. It was found that KCl and NaCl are major contributors than MnSO4, Pb(NO3)2, KI and KBr. The relative increase in corrosion is high in KBr, KI, NaNO3, CaCl2, and less in Pb(NO3)2, NaHCO3 and CaCO3 test solutions. For the reliability of results the data has been statistically analysed.

  3. Aqueous DMSO Mediated Conversion of (2-(Arylsulfonyl)vinyl)iodonium Salts to Aldehydes and Vinyl Chlorides.

    Science.gov (United States)

    Zawia, Eman; Moran, Wesley J

    2016-01-01

    Vinyl(aryl)iodonium salts are useful compounds in organic synthesis but they are under-utilized and their chemistry is under-developed. Herein is described the solvolysis of some vinyl(phenyl)iodonium salts, bearing an arylsulfonyl group, in aqueous DMSO leading to aldehyde formation. This unusual process is selective and operates under ambient conditions. Furthermore, the addition of aqueous HCl and DMSO to these vinyl(aryl)iodonium salts allows their facile conversion to vinyl chlorides. PMID:27537866

  4. Flow-Electrode Capacitive Deionization Using an Aqueous Electrolyte with a High Salt Concentration.

    Science.gov (United States)

    Yang, SeungCheol; Choi, Jiyeon; Yeo, Jeong-Gu; Jeon, Sung-Il; Park, Hong-Ran; Kim, Dong Kook

    2016-06-01

    Flow-electrode capacitive deionization (FCDI) is novel capacitive deionization (CDI) technology that exhibits continuous deionization and a high desalting efficiency. A flow-electrode with high capacitance and low resistance is required for achieving an efficient FCDI system with low energy consumption. For developing high-performance flow-electrode, studies should be conducted considering porous materials, conductive additives, and electrolytes constituting the flow-electrode. Here, we evaluated the desalting performances of flow-electrodes with spherical activated carbon and aqueous electrolytes containing various concentrations of NaCl in the FCDI unit cell for confirming the effect of salt concentration on the electrolyte of a flow-electrode on desalting efficiency. We verified the necessity of a moderate amount of salt in the flow-electrode for compensating for the reduction in the performance of the flow-electrode, attributed to the resistance of water used as the electrolyte. Simultaneously, we confirmed the potential use of salt water with a high salt concentration, such as seawater, as an aqueous electrolyte for the flow-electrode. PMID:27162028

  5. Ion aggregation in high salt solutions. III. Computational vibrational spectroscopy of HDO in aqueous salt solutions.

    Science.gov (United States)

    Choi, Jun-Ho; Kim, Heejae; Kim, Seongheun; Lim, Sohee; Chon, Bonghwan; Cho, Minhaeng

    2015-05-28

    The vibrational frequency, frequency fluctuation dynamics, and transition dipole moment of the O-D stretch mode of HDO molecule in aqueous solutions are strongly dependent on its local electrostatic environment and hydrogen-bond network structure. Therefore, the time-resolved vibrational spectroscopy the O-D stretch mode has been particularly used to investigate specific ion effects on water structure. Despite prolonged efforts to understand the interplay of O-D vibrational dynamics with local water hydrogen-bond network and ion aggregate structures in high salt solutions, still there exists a gap between theory and experiment due to a lack of quantitative model for accurately describing O-D stretch frequency in high salt solutions. To fill this gap, we have performed numerical simulations of Raman scattering and IR absorption spectra of the O-D stretch mode of HDO in highly concentrated NaCl and KSCN solutions and compared them with experimental results. Carrying out extensive quantum chemistry calculations on not only water clusters but also ion-water clusters, we first developed a distributed vibrational solvatochromic charge model for the O-D stretch mode in aqueous salt solutions. Furthermore, the non-Condon effect on the vibrational transition dipole moment of the O-D stretch mode was fully taken into consideration with the charge response kernel that is non-local polarizability density. From the fluctuating O-D stretch mode frequencies and transition dipole vectors obtained from the molecular dynamics simulations, the O-D stretch Raman scattering and IR absorption spectra of HDO in salt solutions could be calculated. The polarization effect on the transition dipole vector of the O-D stretch mode is shown to be important and the asymmetric line shapes of the O-D stretch Raman scattering and IR absorption spectra of HDO especially in highly concentrated NaCl and KSCN solutions are in quantitative agreement with experimental results. We anticipate that this

  6. Liquid-vapor distribution of some amines and acid-ionization constants of their ammonium salts in high temperature aqueous systems

    International Nuclear Information System (INIS)

    Ammonia and volatile organic amines are used to treat the water in steam generating systems to afford protection of the steam and feedwater circuits from corrosion by acidic condensate. The base strength and the volatility of the reagent used are two important parameters that have bearing on its ability to inhibit corrosion; they determine the pH of the solution produced from condensing steam. The distribution of thirteen amines between water and steam in the temperature range 150 to 325 degree C was studied. The amines were chosen on the basis of their known room temperature base strength. The acid ionization constants (Ka) of the ammonium salts of seven of these amines were determined by conductivity measurement in the temperature range 25 to 275 degree C. Amines with high room temperature base strength and distribution coefficient in the optimum range were chosen for the high-temperature base strength determination. The results of these studies were used to estimate the effectiveness of these amines in raising the pH of the condensate from steam containing carbon dioxide and acetic acid in order to provide the basis for further studies on the corrosion inhibition properties of the amines

  7. Mars Aqueous Processing System Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Mars Aqueous Processing System (MAPS) is an innovative method to produce useful building materials from Martian regolith. Acids and bases produced from the regolith...

  8. Mars Aqueous Processing System Project

    Data.gov (United States)

    National Aeronautics and Space Administration — The Mars Aqueous Processing System (MAPS) is a novel technology for recovering oxygen, iron, and other constituents from lunar and Mars soils. The closed-loop...

  9. Diffusion coefficients of β-cyclodextrin sulfated sodium salt in aqueous solutions

    International Nuclear Information System (INIS)

    Graphical abstract: Structure of β-cyclodextrin sulfated sodium salt. - Highlights: • Mutual diffusion coefficients of β-cyclodextrin sulfated sodium salt (NaSO3βCD) in aqueous solutions were measured. • Influence of the viscosity, thermodynamic and temperature factors on the variation of diffusion was analysed. • Estimation of the hydrodynamic radius of NaSO3βCD was obtained. - Abstract: The Taylor dispersion technique has been used for measuring mutual diffusion coefficients of β-cyclodextrin sulfated sodium salt (NaSO3βCD) at temperatures (298.15 and 310.15) K and at finite concentrations. These studies have been complemented by density and viscosity measurements. From these experimental results, the hydrodynamic radius Rh, and its dependence on the viscosity, diffusion coefficient at infinitesimal concentration, D0, ion conductivity of NaSO3βCD and the thermodynamic factor, FT, have been estimated, permitting us to have a better understanding of the structure of the aqueous system containing NaSO3βCD

  10. Compositions for preparation of aqueous solutions of salts of lower valence /sup 99/Tc

    Energy Technology Data Exchange (ETDEWEB)

    Schmidt-Dunker, M.; Greb, W.

    1979-01-09

    Aqueous solutions of /sup 99/Tc salts in which the /sup 99/Tc is in reduced valencey state, when administered to mammals, permit identification of the skeleton and of calcareous tumors by scintigraphy (radiographic scanning). The solutions are conveniently prepared by mixing one or more phosphonic acids (or their salts) with one or more reducing salts, and adding the mixture to an aqueous solution of a pharmaceutically acceptable /sup 99/pertechnetate salt. Reduction of the valence of the technetium occurs rapidly, and the resulting solution is adequately stable for use in scintigraphy. The phosphonic acid and reducing salt components can be premixed. Aqueous solutions of the premix are stable for long periods of time in the absence of free oxygen and the premix is stable to air so long as it is dry.

  11. Measurement of linear attenuation coefficients of gamma rays for some salts by aqueous solution method

    International Nuclear Information System (INIS)

    The linear attenuation coefficients of dilute aqueous solutions of some salts with varying concentrations are measured for different gamma energies (0.36 MeV to 1.33 MeV). From these measurements, linear attenuation coefficients for pure salts are obtained by using the improved technique of Teli (1998). The comparison with theoretical values shows excellent agreement. Half value thicknesses of the salts and total atomic cross sections are also evaluated. (author)

  12. The influence of temperature and inorganic salts on therheological properties of xanthan aqueous solutions

    OpenAIRE

    KATARINA JEREMIC; SINISA MARKOV; BRANISLAV PEKIC; SLOBODAN JOVANOVIC; MIRJANA S. PAVLOVIC

    1999-01-01

    The rheological properties of xanthan gum in aqueous saline solutions and at increased temperatures are of great practical interest especially for its application in enhanced oil recovery during which the xanthan solutions are exposed to increased salt contents and relatively high temperatures. In this work, the influence of high temperature and high salt concentrations (up to 10 mass%) on the rheological properties of xanthan was investigated. The influence of three different salts was exami...

  13. 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

    The Extended UNIQUAC model for electrolyte solutions is an excess Gibbs energy function consisting of a Debye-Huckel term and a term corresponding to the UNIQUAC equation. For vapor-liquid equilibrium calculations, the fugacities of gas-phase components are calculated with the Soave-Redlich-Kwong......-propanol, 2-methyl 2-propanol) and various ions (Na+, K+, NH4+, Cl-, NO3, SO42-, SO32-, HSO3-, CO32-, and HCO3-) shows the capability of the model to accurately represent the phase behavior of these kinds of systems. (C) 2004 Elsevier Ltd. All rights reserved....

  14. Density, viscosity, and N2O solubility of aqueous amino acid salt and amine amino acid salt solutions

    International Nuclear Information System (INIS)

    Highlights: ► Density of amino acid salt and amine amino acid salt. ► Viscosity of amino acid salt and amine amino acid salt. ► Henry’s law constant/N2O solubility of amino acid salt and amine amino acid salt. ► Schumpe model. Correlations for density, viscosity, and N2O solubility. - Abstract: Physicochemical properties of aqueous amino acid salt (AAS), potassium salt of sarcosine (KSAR) and aqueous amine amino acid salt (AAAS), 3-(methylamino)propylamine/sarcosine (SARMAPA) have been studied. Densities of KSAR were measured for sarcosine mole fraction 0.02 to 0.25 for temperature range 298.15 K to 353.15 K, the viscosities were measured for 0.02 to 0.10 mole fraction sarcosine (293.15 K to 343.15 K) while the N2O solubilities were measured from 0.02 to 0.10 mole fraction sarcosine solutions (298.15 K to 363.15 K). Densities of SARMAPA were measured for sarcosine mole fraction 0.02 to 0.23 for temperature range (298.15 K to 353.15 K), viscosities were measured for 0.02 to 0.16 mole fraction sarcosine (293.15 K to 343.15 K) while the N2O solubilities were measured from 0.02 to 0.16 mole fraction sarcosine solutions (298.15 K to 343.15 K). Experimental results were correlated well with empirical correlations and N2O solubility results for KSAR were predicted adequately by a Schumpe model. The solubilities of N2O in AAS and AAAS are significantly lower than values for amines. The solubilities vary as: amine > AAAS > AAS.

  15. Electrosorption of inorganic salts from aqueous solution using carbon aerogels.

    Science.gov (United States)

    Gabelich, Christopher J; Tran, Tri D; Suffet, I H Mel

    2002-07-01

    Capacitive deionization (CDI) with carbon aerogels has been shown to remove various inorganic species from aqueous solutions, though no studies have shown the electrosorption behavior of multisolute systems in which ions compete for limited surface area. Several experiments were conducted to determine the ion removal capacity and selectivity of carbon aerogel electrodes, using both laboratory and natural waters. Although carbon aerogel electrodes have been treated as electrical double-layer capacitors, this study showed that ion sorption followed a Langmuir isotherm, indicating monolayer adsorption. The sorption capacity of carbon aerogel electrodes was approximately 1.0-2.0 x 10(-4) equiv/g aerogel, with ion selectivity being based on ionic hydrated radius. Monovalent ions (e.g., sodium) with smaller hydrated radii were preferentially removed from solution over multivalent ions (e.g., calcium) on a percent or molar basis. Because of the relatively small average pore size (4-9 nm) of the carbon aerogel material, only 14-42 m2/g aerogel surface area was available for ion sorption. Natural organic matter may foul the aerogel surface and limit CDI effectiveness in treating natural waters. PMID:12144279

  16. Sub-0.5 V Highly Stable Aqueous Salt Gated Metal Oxide Electronics

    OpenAIRE

    Sungjun Park; SeYeong Lee; Chang-Hyun Kim; Ilseop Lee; Won-June Lee; Sohee Kim; Byung-Geun Lee; Jae-Hyung Jang; Myung-Han Yoon

    2015-01-01

    Recently, growing interest in implantable bionics and biochemical sensors spurred the research for developing non-conventional electronics with excellent device characteristics at low operation voltages and prolonged device stability under physiological conditions. Herein, we report high-performance aqueous electrolyte-gated thin-film transistors using a sol-gel amorphous metal oxide semiconductor and aqueous electrolyte dielectrics based on small ionic salts. The proper selection of channel ...

  17. Salt Crystallization from an Evaporating Aqueous Solution by Molecular Dynamics Simulations

    Czech Academy of Sciences Publication Activity Database

    Mucha, Martin; Jungwirth, Pavel

    2003-01-01

    Roč. 107, č. 33 (2003), s. 8271-8274. ISSN 1089-5647 R&D Projects: GA MŠk LN00A032 Institutional research plan: CEZ:AV0Z4040901 Keywords : salt crystallization * aqueous solution * molecular dynamics Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.679, year: 2003

  18. Kinetic study of CO2 with various amino acid salts in aqueous solution

    NARCIS (Netherlands)

    Holst, van J.; Versteeg, G.F.; Brilman, D.W.F.; Hogendoorn, J.A.

    2009-01-01

    A study towards the kinetics of CO2 with several aqueous salts of amino acids was performed at a temperature of 298 K. Absorption rate experiments were carried out in the pseudo-first-order regime, enabling the determination of the kinetic rate constant from the flux. In a preliminary screening at a

  19. Kinetic study of CO2 with various amino acid salts in aqueous solution

    NARCIS (Netherlands)

    van Hoist, J.; Versteeg, G. F.; Brilman, D. W. F.; Hogendoorn, J. A.; Holst, J. v

    2009-01-01

    A study towards the kinetics Of CO2 with several aqueous salts of amino acids was performed at a temperature of 298 K. Absorption rate experiments were carried out in the pseudo-first-order regime, enabling the determination of the kinetic rate constant from the flux. In a preliminary screening at a

  20. Discontinuous hygroscopic growth of an aqueous surfactant/salt aerosol particle levitated in an electrodynamic balance

    Science.gov (United States)

    Soonsin, V.; Krieger, U. K.; Peter, T.

    2010-12-01

    Organic compounds are a major fraction of tropospheric aerosol. The organic fraction is usually internally mixed with inorganic salts. Surface-active organic matter or surfactants, enriched in the oceanic surface layer and transferred to the atmosphere by bubble-bursting processes, are the most likely candidates to contribute the observed organic fraction in sea salt aerosol [1, 2]. If the organic substance is a surfactant, it will lower the surface tension. In addition aggregates of the organic monomers, called micelles, will form if the concentration of the organic exceeds a certain limit (critical micelle concentration). These aggregates do have different morphology (spheres or globular or rod like micelles, or spherical bilayer vesicles etc.) and size, depending on the nature of the organic molecule, its concentration and the concentration of inorganic salts [3]. These aggregate may promote solubilisation of organic compounds in aqueous atmospheric aerosol. We performed measurements of ternary aqueous solution particles consisting of tetraethylene glycol monooctyl ether (C8E4) as organic surfactant and sodium chloride (NaCl) as inorganic salt and water (H2O) using single levitated aerosol particles in an electrodynamic balance. The particles can be stored contact-free in a temperature and humidity controlled chamber and optical resonance spectroscopy is used to monitor radius change [4]. Mie resonance spectra of ternary droplets show discontinuous growth with increasing relative humidity (RH) and also discontinuous shrinkage with decreasing relative humidity. We observe this behavior at temperatures and RHs at which the salt is completely deliquesced and the concentration of the organic surfactant is larger than the critical micelle concentration. Independent measurements of particle mass show also discontinuous water uptake. We speculate that this discontinuous, step-like, growth is caused by disaggregation of a micelle needed to conserve the monolayer of

  1. Study on Properties and Structural Parameters of Microemulsion CTAB/Butanol/Cyclohexane/Salt Aqueous Solution

    Institute of Scientific and Technical Information of China (English)

    Chen Yongjie; Qiu Guanming; Tian Yiguang; Fang Li; Xiao Linjiu; Sun Yanbin

    2005-01-01

    The phase diagrams of microemulsion CTAB/butanol/cyclohexane/aqueous solution of nitrate (or aqueous solution of ammonium salt) were determined and the structural parameters and ΔG*o→i were obtained by means of dilution method and theoretical calculation. The effect of different w/s and salt concentration on the stability and structural parameters of microemulsion were investigated. The result shows that with the increase of w/s, the area of microemulsion and Nd decrease, Rw, l and n increase; with the increase of salt concentration, the area of microemulsion, l and Nd decrease, ΔG*o→I, Rw and n increase. Theoretical basis of preparing size-controlled long afterglow luminescence materials and study of the relationship between fluorescence properties and particle size are provided.

  2. Densities, viscosities, refractive indices, and electrical conductivities of aqueous alkali salts of α-alanine

    International Nuclear Information System (INIS)

    Highlights: • Thermophysical properties of aqueous Na and K salts of α-alanine were studied. • Properties are density, viscosity, refractive indices, and thermal conductivity. • The concentrations of amino acid salt ranges from (0.5 to 3.5) M. • The temperature range studied was (333.15 to 343.15) K. • The measured data were represented satisfactorily by using the applied correlations. - Abstract: In this work, physicochemical properties such as density, viscosity, refractive index, and electrical conductivity of aqueous alkali (potassium or sodium) salts of the amino acid α-alanine (ALA), were measured at temperatures from (303.15 to 343.15) K and concentrations ranging from (0.5 to 3.5) M. Density and viscosity measurements were performed using the vibrating tube and the falling ball techniques, respectively. The refractive index at the sodium D line was measured in an automatic refractometer, while the electrical conductivity was measured using a commercial conductivity meter. An empirical equation was applied to correlate the density, refractive index, and electrical conductivity of the amino acid salt solutions with temperature and amino acid salt concentration, which gave average absolute deviation values of 0.03%, 0.01%, and 0.6%, respectively. The variation of the viscosity as a function of temperature and amino acid salt concentration was accurately represented by a modified Vogel–Tamman–Fulcher equation at an average absolute deviation of 0.5%

  3. Surface Crystallization of Aqueous Salt Solution Under Overheating and Overcooling

    Directory of Open Access Journals (Sweden)

    Nakoryakov Vladimir

    2016-01-01

    Full Text Available The investigation of the surface crystallization with low negative and high positive temperatures were carried in the paper. Crystallization curves for distillate (Ts0 = −9 °C and different mass salt concentrations NaCl (Ts0 = 80 °C were obtained. Experimental data indicate that the crystallization centers influence each other and the number of centers does not change with time. The maximum speeds for the crystallization front reached 0.3–0.5 m/s. There are a significant anisotropy and a curvature of crystallization front. The surface kinetics should be considered to clarify the rate of freezing and melting of ice in modeling global warming.

  4. Theoretical analysis of XANES for aqueous aluminum salt solutions

    Science.gov (United States)

    Matsuo, Shuji; Shirozu, Kaori; Tateishi, Yuichi; Wakita, Hisanobu; Yokoyama, Takushi

    In order to understand the coordination behavior of Al(III) ions in hydrosphere, discrete variational X[alpha] molecular orbital calculations were performed to analyze Al K-edge XANES spectra for the aqueous solutions of Al(NO3)3·9H2O and Al-EDTA (EDTA = ethylenediaminetetraacetate) complex. As to Al(NO3)3·9H2O, the hydrate structure was presumed to be rather an asymmetric hexahydrated structure than an high-symmetric structure. As to Al-EDTA, the 5-fold coordinated Al-EDTA was concluded to be the coexistence of the pyramidal and trigonal bipyramidal structures in proportion of 4 to 6.

  5. Infrared spectroscopy of aqueous ionic salt mixtures at low concentrations: ion pairing in water.

    Science.gov (United States)

    Max, Jean-Joseph; Chapados, Camille

    2007-09-21

    The analysis by infrared spectroscopy of aqueous mixtures of NaI and CsCl was made in order to obtain information at the molecular level of the mixing of these two salts taken as model systems of strong electrolytes in water. In previous papers [J.-J. Max and C. Chapados, J. Chem. Phys. 115, 2664 (2001) and J.-J. Max et al., ibid. 126, 184507 (2007)] it was reported that a pure salt in water forms pairs of monoions to which are attached a fixed number of water molecules, giving solvated water species. Due to their interaction with the ion pairs, the solvated water molecules are strongly perturbed, modifying the IR water spectrum being monitored. After taking the IR spectrum of pure water, a small volume of NaI 2M was added and the IR spectrum taken. Then a small volume of CsCl 2M was added and a new IR spectrum taken. This procedure was repeated to obtain a series of 38 spectra in the 0.05M-0.83M concentration range. Factor analysis made on the series revealed the presence of three types of water: pure water and two salt solvated waters. The number of solvated water molecules on the two salts taken together is ten. Since NaI and CsCl have, respectively, 3.5 and 3.0 solvated water molecules, it was concluded that a reaction occurred in the solutions forming NaCl and CsI that have, respectively, five water molecules each for a total of ten. The analysis of the spectra of the orthogonal factors supports this attribution. These results provide additional proof of ion pairing in water. Furthermore, comparing the band displacements and intensity variations observed on the solvated water species to that of pure water indicates that the dielectric milieu surrounding the ion pairs is not constant. These results do not support the classical view of Debye-Huckel that considers that the ions are independent and the dielectric milieu constant. The present results give some in situ information on the reaction that goes on in "simple" electrolyte systems whose reactivity and

  6. Determination of particle size distribution of salt crystals in aqueous slurries. [From reprocessing of fuel elements

    Energy Technology Data Exchange (ETDEWEB)

    Miller, A.G.

    1977-10-01

    A method for determining particle size distribution of water-soluble crystals in aqueous slurries is described. The salt slurries, containing sodium salts of predominantly nitrate, but also nitrite, sulfate, phosphate, aluminates, carbonate, and hydroxide, occur in radioactive, concentrated chemical waste from the reprocessing of nuclear fuel elements. The method involves separating the crystals from the aqueous phase, drying them, and then dispersing the crystals in a nonaqueous medium based on nitroethane. Ultrasonic treatment is important in dispersing the sample into its fundamental crystals. The dispersed crystals are sieved into appropriate size ranges for counting with a HIAC brand particle counter. A preponderance of very fine particles in a slurry was found to increase the difficulty of effecting complete dispersion of the crystals because of the tendency to retain traces of aqueous mother liquor. Traces of moisture produce agglomerates of crystals, the extent of agglomeration being dependent on the amount of moisture present. The procedure is applicable to particles within the 2 to 600 ..mu..m size range of the HIAC particle counter. The procedure provides an effective means for measuring particle size distribution of crystals in aqueous salt slurries even when most crystals are less than 10 ..mu..m in size. 19 figures.

  7. Influence of Salts on Electrospinning of Aqueous and Nonaqueous Polymer Solutions

    Directory of Open Access Journals (Sweden)

    Fatma Yalcinkaya

    2015-01-01

    Full Text Available A roller electrospinning system was used to produce nanofibres by using different solution systems. Although the process of electrospinning has been known for over half a century, knowledge about spinning behaviour is still lacking. In this work, we investigated the effects of salt for two solution systems on spinning performance, fibre diameter, and web structure. Polyurethane (PU and polyethylene oxide (PEO were used as polymer, and tetraethylammonium bromide and lithium chloride were used as salt. Both polymer and salt concentrations had a noteworthy influence on the spinning performance, morphology, and diameter of the nanofibres. Results indicated that adding salt increased the spinnability of PU. Salt created complex bonding with dimethylformamide solvent and PU polymer. Salt added to PEO solution decreased the spinning performance of fibres while creating thin nanofibres, as explained by the leaky dielectric model.

  8. Aminoguanidinium closo-borates and their reactions with copper(2) salts in aqueous solutions

    International Nuclear Information System (INIS)

    Amino guanidine hexa-, deca- and dodecaborates of the (AguH)2BnHn · xH2O, where Agu - (CN4H6); n = 6, 10, 12; x = 1, 2, composition were synthesized and defined by means of element, magnetic susceptibility and IR spectroscopy analyses. Their reaction with the copper(2) salts in aqueous solutions was studied. It was shown that cation-anion interaction, which was enhanced in the B12 10 6 row, were the case in the amino guanidine closo-borates. The reaction of the amino guanidine closo-borates with the copper(2) salts in aqueous solutions leads to formation either complexes (n = 10, 12) or elemental copper (in the case of B6H62- anion) depending on closo-borate anion BnHn2-

  9. On the attenuation of X-rays and gamma-rays for aqueous solutions of salts

    CERN Document Server

    Teli, M T

    1998-01-01

    Disparities in the linear attenuation coefficients of X-rays and gamma rays for aqueous solutions of soluble salts arising from the nonequality of volume of the solution with the sum of volumes of its components are analysed and the mixture rule is reformulated. The disparities are illustrated for NaCl solution for concentrations c=0 to 1 gm/cm sup 3 which indicates that the mixture rule of Teli et al. works well within generally acceptable limits.

  10. Thermophysical property characterization of aqueous amino acid salt solutions containing α-aminobutyric acid

    International Nuclear Information System (INIS)

    Highlights: • Thermophysical properties of aqueous potassium and sodium salt solutions of α-aminobutyric acid were studied. • Density, electrolytic conductivity, refractive index, and viscosity of the solution were measured. • The concentrations of amino acid salt ranges from x1 = 0.009 to 0.06. • The temperature range studied was (303.15 to 343.15) K. • The measured data were represented satisfactorily by using the applied correlations. - Abstract: In this study, density, electrical conductivity, refractive index and viscosity of aqueous potassium and sodium salt solutions of α-aminobutyric acid were presented. Measurements were done over the temperature range (303.15 to 343.15) K and atmospheric pressure for salt compositions from x1 = 0.009 to 0.062. A modified Graber et al. equation was used to correlate the density, electrical conductivity, and refractive index with temperature and composition leading to average absolute deviations (AAD) between the predicted and calculated values of 0.04%, 0.7%, and 0.01%, respectively. The viscosity data were represented as a function of temperature and composition via Vogel–Tamman–Fulcher (VTF) type equation at an AAD of 0.6%

  11. Study on Properties of Microemulsion AEO-9/Butanol/Cyclohexane/Salt Aqueous Solution

    Institute of Scientific and Technical Information of China (English)

    Qiu Guanming; Chen Yongjie; Tian Yiguang; Fang Li; Xiao Linjiu; Sun Yanbin

    2004-01-01

    The microemulsion AEO-9/butanol/cyclohexane/nitrate aqueous solution (or ammonium salt aqueous solution) was studied, which was used as 'micro-reactor' in preparing long afterglow phosphor materials SrAl2O4: Eu2+ ,Dy3+. The phase behavior of microemulsion was investigated. The radius of inner water droplet Rw and the change of standard free energy ΔG*o→i were obtained by means of dilution method and theoretical calculation. The result shows that with the increase of W/S, the area of microemulsion region decreases, Rw and ΔG*o→i increase and the microemulsion stability decreases. The structure change and formation area of microemulsion AEO-9/butanol/cyclohexane/nitrate aqueous solution ( or ammonium salt aqueous solution) were offered for the adoption of a synthesis method with newly high efficiency and utility. The particular size and its distribution theory gist, fluorescence life-span, and quenching concentration parameter data were expected. A new approach was explored for finding a new preparation method of rare earths afterglow materials and increasing luminescence intensity without crashing.

  12. (Surfactant + polymer) interaction parameter studied by (liquid + liquid) equilibrium data of quaternary aqueous solution containing surfactant, polymer, and salt

    International Nuclear Information System (INIS)

    (Liquid + liquid) equilibrium (LLE) data of quaternary aqueous system containing polyoxyethylene (20) cetyl ether (with abbreviation name Brij 58, non-ionic surfactant), diammonium hydrogen phosphate, and poly ethylene glycol (PEG) with three molar masses {MW = (1000, 6000, and 35,000) g . mol-1} have been determined experimentally at T = 313.15 K. Furthermore, the Flory-Huggins theory with two electrostatic terms (Debye-Hueckel and Pitzer-Debye-Hueckel equations) have been used to calculate the phase behavior of the quaternary systems and (surfactant + polymer) interaction parameter as well as interaction parameters between other species. Temperature dependency of the parameters of the Flory-Huggins theory has been obtained. Also an effort have been done to show that addition of PEG as well as increasing the temperature can shift the binodal curves of the ternary aqueous system containing surfactant and salt to lower mole fraction of salt. Also the effect of polymer molar mass on the binodal diagram displacement has been discussed

  13. (Surfactant + polymer) interaction parameter studied by (liquid + liquid) equilibrium data of quaternary aqueous solution containing surfactant, polymer, and salt

    Energy Technology Data Exchange (ETDEWEB)

    Foroutan, Masumeh [Physical Chemistry Department, School of Chemistry, College of Science, University of Tehran, 14155-6455 Tehran (Iran, Islamic Republic of)], E-mail: foroutan@khayam.ut.ac.ir; Heidari, Nosrat; Mohammadlou, Maryam [Chemistry Department, Faculty of Science, Uremia University, Uremia (Iran, Islamic Republic of); Sojahrood, Amin Jafari [Physics Department, Faculty of Science, Uremia University, Uremia (Iran, Islamic Republic of)

    2009-02-15

    (Liquid + liquid) equilibrium (LLE) data of quaternary aqueous system containing polyoxyethylene (20) cetyl ether (with abbreviation name Brij 58, non-ionic surfactant), diammonium hydrogen phosphate, and poly ethylene glycol (PEG) with three molar masses {l_brace}M{sub W} = (1000, 6000, and 35,000) g . mol{sup -1}{r_brace} have been determined experimentally at T = 313.15 K. Furthermore, the Flory-Huggins theory with two electrostatic terms (Debye-Hueckel and Pitzer-Debye-Hueckel equations) have been used to calculate the phase behavior of the quaternary systems and (surfactant + polymer) interaction parameter as well as interaction parameters between other species. Temperature dependency of the parameters of the Flory-Huggins theory has been obtained. Also an effort have been done to show that addition of PEG as well as increasing the temperature can shift the binodal curves of the ternary aqueous system containing surfactant and salt to lower mole fraction of salt. Also the effect of polymer molar mass on the binodal diagram displacement has been discussed.

  14. Aqueous systems and geothermal energy

    International Nuclear Information System (INIS)

    Significant unpublished results reported include: osmotic coefficients of KCl solutions vs. molality at 109 to 2010C; cadmium ion diffusivities in CaCl2 hydrous melts; a x-ray diffraction study of the uranyl complex in water; solubility of amorphous silica in aqueous NaNO3 solutions at 100 to 3000C; and corrosion of carbon steel by geothermal brine

  15. Electrostatic interactions and aqueous two-phase separation modes of aqueous mixed oppositely charged surfactants system.

    Science.gov (United States)

    Hao, Li-Sheng; Gui, Yuan-Xiang; Chen, Yan-Mei; He, Shao-Qing; Nan, Yan-Qing; You, Yi-Lan

    2012-08-30

    Electrostatic interactions play an important role in setting the aqueous two-phase separation behaviors of mixtures of oppositely charged surfactants. The aqueous mixture of cetyltrimethylammonium bromide (CTAB) and sodium dodecylsulfonate (AS) is actually a five-component system, comprised of CTAB, AS, complex salt (cetyltrimethylammonium dodecylsulfonate, abbreviated as CTA(+)AS(-)), NaBr, and water. In the three-dimensional pyramid phase diagram, the aqueous two-phase region with excess AS or with excess CTAB extends successively from the region very near to the NaBr-H2O line through the CTAB-AS-H2O conventional mixing plane to the CTA(+)AS(-)-AS-H2O side plane or to the CTA(+)AS(-)-CTAB-H2O side plane, respectively. Large or small molar ratios between the counterions and their corresponding surfactant ions for oppositely charged surfactants located in the NaBr side or the CTA(+)AS(-) side of the pyramid imply strong or weak electrostatic screening. Electrostatic screening of counterions alters the electrostatic attractions between the oppositely charged head groups or the electrostatic repulsions between the like-charged head groups in excess, and the electrostatic free energy of aggregation thus affects the aqueous two-phase separation modes. Composition analysis, rheological property investigation, and TEM images suggest that there are two kinds of aqueous two-phase systems (ATPSs). On the basis of these experimental results and Kaler's cell model, two kinds of phase separation modes were proposed. Experimental results also indicate that all of the top phases are surfactant-rich, and all of the bottom phases are surfactant-poor; the density difference between the top phase and the bottom phase in one ATPS is very small; the interfacial tension (σ) of the ATPS is ultralow. PMID:22856887

  16. A Layout for the Carbon Capture with Aqueous Ammonia without Salt Precipitation

    DEFF Research Database (Denmark)

    Bonalumi, Davide; Valenti, Gianluca; Lillia, Stefano;

    2016-01-01

    Post-combustion carbon capture technologies seem to be necessary to realize the CO2 mitigation policies internationally shared for the next future, despite none of them appears to be ready for full-scale applications. This work considers the aqueous ammonia based process for a coal-fired Ultra...... Super Critical power plant. Two layouts are simulated with Aspen Plus employing the recently recalibrated Extended UNIQUAC thermodynamic model. The first one operates at chilling conditions, which yield to salt precipitation, and is taken as reference because already analyzed in previous studies......, a lower SPECCA of 2.58 MJ/kgco2. The latter layout is a better choice also from the perspective of the plant operation since it does not present the salt precipitation....

  17. Investigation of the Ionic Hydration in Aqueous Salt Solutions by Soft X-ray Emission Spectroscopy.

    Science.gov (United States)

    Jeyachandran, Y L; Meyer, F; Benkert, A; Bär, M; Blum, M; Yang, W; Reinert, F; Heske, C; Weinhardt, L; Zharnikov, M

    2016-08-11

    Understanding the molecular structure of the hydration shells and their impact on the hydrogen bond (HB) network of water in aqueous salt solutions is a fundamentally important and technically relevant question. In the present work, such hydration effects were studied for a series of representative salt solutions (NaCl, KCl, CaCl2, MgCl2, and KBr) by soft X-ray emission spectroscopy (XES) and resonant inelastic soft X-ray scattering (RIXS). The oxygen K-edge XES spectra could be described with three components, attributed to initial state HB configurations in pure water, water molecules that have undergone an ultrafast dissociation initiated by the X-ray excitation, and water molecules in contact with salt ions. The behavior of the individual components, as well as the spectral shape of the latter component, has been analyzed in detail. In view of the role of ions in such effects as protein denaturation (i.e., the Hofmeister series), we discuss the ion-specific nature of the hydration shells and find that the results point to a predominant role of anions as compared to cations. Furthermore, we observe a concentration-dependent suppression of ultrafast dissociation in all salt solutions, associated with a significant distortion of intact HB configurations of water molecules facilitating such a dissociation. PMID:27442708

  18. Characterization of reaction products of iron and iron salts and aqueous plant extracts

    International Nuclear Information System (INIS)

    The complexes formed in aqueous solution as a result of a reaction of iron and iron salts (Fe2+ and Fe3+) and some plant extracts were analyzed using Moessbauer spectroscopy and Fourier transform infrared. The extracts were obtained from Opuntia elatior mill., Acanthocereus pentagonus (L.) Britton, Mimosa tenuiflora, Caesalpinia coriaria (Jacq.) Willd., Bumbacopsis quinata (Jacq.) Dugand and Acacia mangium Willd., plants growing wildly in different zones of the Isthmus of Panama. Results suggest the formation of mono- and bis-type complexes, and in some cases, the occurrence of a redox reaction. The feasibility of application of the studied extracts as atmospheric corrosion inhibitors is discussed

  19. Characterization of reaction products of iron and iron salts and aqueous plant extracts

    Science.gov (United States)

    Jaén, J. A.; García de Saldaña, E.; Hernández, C.

    1999-11-01

    The complexes formed in aqueous solution as a result of a reaction of iron and iron salts (Fe2+ and Fe3+) and some plant extracts were analyzed using Mössbauer spectroscopy and Fourier transform infrared. The extracts were obtained from Opuntia elatior mill., Acanthocereus pentagonus (L.) Britton, Mimosa tenuiflora, Caesalpinia coriaria (Jacq.) Willd., Bumbacopsis quinata (Jacq.) Dugand and Acacia mangium Willd., plants growing wildly in different zones of the Isthmus of Panama. Results suggest the formation of mono- and bis-type complexes, and in some cases, the occurrence of a redox reaction. The feasibility of application of the studied extracts as atmospheric corrosion inhibitors is discussed.

  20. Characterization of reaction products of iron and iron salts and aqueous plant extracts

    Energy Technology Data Exchange (ETDEWEB)

    Jaen, J.A. [Universidad de Panama, Centro de Investigaciones con Tecnicas Nucleares/Depto. de Quimica (Panama); Garcia de Saldana, E.; Hernandez, C. [Universidad de Panama, Maestria en Ciencias Quimicas (Panama)

    1999-11-15

    The complexes formed in aqueous solution as a result of a reaction of iron and iron salts (Fe{sup 2+} and Fe{sup 3+}) and some plant extracts were analyzed using Moessbauer spectroscopy and Fourier transform infrared. The extracts were obtained from Opuntia elatior mill., Acanthocereus pentagonus (L.) Britton, Mimosa tenuiflora, Caesalpinia coriaria (Jacq.) Willd., Bumbacopsis quinata (Jacq.) Dugand and Acacia mangium Willd., plants growing wildly in different zones of the Isthmus of Panama. Results suggest the formation of mono- and bis-type complexes, and in some cases, the occurrence of a redox reaction. The feasibility of application of the studied extracts as atmospheric corrosion inhibitors is discussed.

  1. Kinetics of absorption of carbon dioxide into aqueous potassium salt of proline

    DEFF Research Database (Denmark)

    Paul, Subham; Thomsen, Kaj

    2012-01-01

    with KPr for the above mentioned concentration and temperature range. Following the reaction mechanism of CO2 with primary and secondary alkanolamies, the reaction of CO2 with KPr is also described using zwitterionic mechanism. Based on the pseudo-first-order condition for the CO2 absorption, the......The absorption of carbon dioxide (CO2) into aqueous solution of potassium prolinate (KPr) are studied at 303, 313, and 323K within the salt concentration range of 0.5–3.0kmolm−3 using a wetted wall column absorber. The experimental results are used to interpret the kinetics of the reaction of CO2...

  2. Correlations for the partition behavior of proteins in aqueous two-phase systems

    DEFF Research Database (Denmark)

    Schmidt, A.S.; Andrews, B.A.; Asenjo, J.A.

    1996-01-01

    The effect of protein concentration in partitioning in PEG/ salt aqueous two-phase systems has been investigated. PEG 4000/phosphate systems in the presence of 0% w/w and 8.8% w/w NaCl have been evaluated using amyloglucosidase, subtilisin, and trypsin inhibitor. Also, a PEG 4000/phosphate system...

  3. Carbon dioxide solubility in aqueous potassium salt solutions of L-proline and DL-α-aminobutyric acid at high pressures

    International Nuclear Information System (INIS)

    Highlights: • CO2 solubility in aqueous potassium salt solutions of L-proline and DL-α-aminobutyric acid were studied. • The CO2 partial pressures studied was up to 1000 kPa. • The temperatures studied were (313.2, 333.2, 353.2) K. • The measured data were represented satisfactorily by using the applied correlations. • The CO2 absorption capacity of the studied systems was high and comparable with monoethanolamine. - Abstract: In the present work, the solubility of CO2 in aqueous solutions of potassium prolinate (KPr) and potassium α-aminobutyrate (KAABA) was measured at temperatures (313.2, 333.2, and 353.2) K and CO2 partial pressures up to 1000 kPa for amino acid salt concentrations: KPr, w = (7.5, 14.5, and 27.4 wt%) and KAABA, w = (6.9, 13.4, and 25.6 wt%). It was found that the CO2 absorption capacities of the studied amino acid salt systems were considerably high and comparable with that of industrially important alkanolamines including monoethanolamine. The CO2 loadings in aqueous potassium α-aminobutyrate at high pressures were also found to be generally higher than the loadings in aqueous potassium prolinate. A modified Kent–Eisenberg model was applied to correlate the CO2 solubility in the amino acid salt solution as function of CO2 partial pressure, temperature, and concentration. The model gave good representation of the (vapour + liquid) equilibrium data obtained for the amino acid salt systems studied, and provided accurate predictions of the solubility

  4. Aqueous two-phase system based on natural quaternary ammonium compounds for the extraction of proteins.

    Science.gov (United States)

    Zeng, Chao-Xi; Xin, Rui-Pu; Qi, Sui-Jian; Yang, Bo; Wang, Yong-Hua

    2016-02-01

    Aqueous two-phase systems, based on the use of natural quaternary ammonium compounds, were developed to establish a benign biotechnological route for efficient protein separation. In this study, aqueous two-phase systems of two natural resources betaine and choline with polyethyleneglycol (PEG400/600) or inorganic salts (K2 HPO4 /K3 PO4 ) were formed. It was shown that in the K2 HPO4 -containing aqueous two-phase system, hydrophobic interactions were an important driving force of protein partitioning, while protein size played a vital role in aqueous two-phase systems that contained polyethylene glycol. An extraction efficiency of more than 90% for bovine serum albumin in the betaine/K2 HPO4 aqueous two-phase system can be obtained, and this betaine-based aqueous two-phase system provided a gentle and stable environment for the protein. In addition, after investigation of the cluster phenomenon in the betaine/K2 HPO4 aqueous two-phase systems, it was suggested that this phenomenon also played a significant role for protein extraction in this system. The development of aqueous two-phase systems based on natural quaternary ammonium compounds not only provided an effective and greener method of aqueous two-phase system to meet the requirements of green chemistry but also may help to solve the mystery of the compartmentalization of biomolecules in cells. PMID:26447826

  5. Molecular dynamics studies of aqueous silica nanoparticle dispersions: salt effects on the double layer formation.

    Science.gov (United States)

    de Lara, Lucas S; Rigo, Vagner A; Michelon, Mateus F; Metin, Cigdem O; Nguyen, Quoc P; Miranda, Caetano R

    2015-08-19

    The ion distribution around hydroxylated silica nanoparticles (NP-H) dispersed in brine was investigated by fully atomistic molecular dynamics. The NP-H dispersions in aqueous electrolyte media are simulated in solutions of varying salinity (NaCl, CaCl2, and MgCl2), salt concentration (0.06  ×  10(-3) to 3.00  ×  10(-3) mole fraction [Formula: see text]), and temperature (300 and 350 K) at 1 atm. The NP-H models reproduce the observed experimental concentration of silanol and geminal surface sites, which are responsible for local charge variations on the nanoparticles' surface. Interestingly, under certain salt concentration conditions, the formation of an electrical double layer (DL) around the overall neutral NP-H occurs. The resulting DLs are attenuated with increasing temperature for all evaluated salts. With increasing salt concentration, a sign inversion of the effective charge at the first ion layer is observed, which modifies the electrostatic environment around the nanoparticle. The minimum salt concentration that leads to a DL formation at 300 K is 1.05  ×  10(-3), 0.37  ×  10(-3), and 0.06  ×  10(-3) χs for NaCl, CaCl2, and MgCl2, respectively. The width of the DL decreases sequentially in ionic strength from NaCl to CaCl2 to MgCl2, which is similar to that found for highly charged surfaces. These results are in line with our previous experimental data for negative charged NP-H. All together, these observations suggest an interplay mechanism between the formation and narrowing of electric double layers on the stability of NP dispersions in both neutral and negatively charged NP-H. PMID:26194994

  6. Adsorption of phenol from aqueous systems onto spent oil shale

    Energy Technology Data Exchange (ETDEWEB)

    Darwish, N.A.; Halhouli, K.A.; Al-Dhoon, N.M. [Jordan Univ. of Science and Technology, Irbid (Jordan)

    1996-03-01

    To evaluate its ability to remove phenol from aqueous solution, Jordanian {open_quotes}spent{close_quotes} oil shale, an abundant natural resource, has been used in an experimental adsorption study. Equilibrium of the system has been determined at three temperatures: 30, 40, and 55{degrees}C. The resulting experimental equilibrium isotherms are well represented by Frendlich, Langmuir, and Redlich-Peterson isotherms. The relevant parameters for these isotherms, as regressed from the experimental equilibrium data, are presented. Effects of solution pH (in the range of 3-11), in addition to effects of three inorganic salts (Kl, KCl, and NaCl), on the equilibrium isotherms were also investigated. The effects of pH in the presence of KI and NaCl were also investigated for a possible interaction between salts and solution pH. The initial concentration of phenol in the aqueous system studied ranges from 10 to 200 ppm. Experimental results show that while an acidic solution has no effect on the adsorption capacity of spent oil shale to phenol, a highly basic solution reduces its adsorbability. No sound effect was observed for the inorganic salts studied on the adsorption of phenol on spent oil shale. The experimental results show that there is no interaction between the pH of solution and the presence of salts. In spite of its ability to remove phenol, spent oil shale showed a very low equilibrium capacity (of an order of magnitude of 1 mg/g). Should the adsorption capacity of the shale be improved (by different treatment processes, such as grafting, surface conditioning), results of this study will find a direct practical implication in serving as {open_quotes}raw{close_quotes} reference data for comparison purposes.

  7. Molecular Dynamics Studies of Concentrated Binary Aqueous Solutions of Lanthanide Salts: Structures and Exchange Dynamics

    International Nuclear Information System (INIS)

    Concentrated binary aqueous solutions of lanthanide (Nd3+ and Dy3+) salts (ClO4-, Cl-, and NO3-) have been studied by means of classical molecular dynamics (MD) simulations with explicit polarization and UV-visible spectroscopy. Pair interaction potentials, used for the MD simulations, have been developed in order to reproduce experimental hydration properties. Nd3+ and Dy3+ have been chosen because of their position in the lanthanide series: Nd3+ being a light lanthanide and Dy3+ a heavy one. They are respectively coordinated to nine and eight water molecules, in pure water, involving changes in their salt hydration structures. Both MD simulations and UV-visible experiments highlight the stronger affinity of nitrate anions toward Ln3+ compared to perchlorates and chlorides. Dissociation/association processes of Nd3+-Cl- and Nd3+-NO3- ion pairs in aqueous solution have been analyzed using potential of mean force profile calculations. Furthermore, from MD simulations, it appears that the affinity of anions (perchlorate, chloride, and nitrate. ) is stronger for Nd3+ than Dy3+. (authors)

  8. Non-monotonic course of protein solubility in aqueous polymer-salt solutions can be modeled using the sol-mxDLVO model.

    Science.gov (United States)

    Herhut, Marcel; Brandenbusch, Christoph; Sadowski, Gabriele

    2016-02-01

    Protein purification is often performed using cost-intensive chromatographic steps. To discover economic alternatives (e.g., crystallization), knowledge on protein solubility as a function of temperature, pH, and additives in solution as well as their concentration is required. State-of-the-art models for predicting protein solubility almost exclusively consider aqueous salt systems, whereas "salting-in" and "salting-out" effects induced by the presence of an additional polymer are not considered. Thus, we developed the sol-mxDLVO model. Using this newly developed model, protein solubility in the presence of one salt and one polymer, especially the non-monotonic course of protein solubility, could be predicted. Systems considered included salts (NaCl, Na-p-Ts, (NH(4))(2) SO(4)) and the polymer polyethylene glycol (MW: 2000 g/mol, 12000 g/mol) and proteins lysozyme from chicken egg white (pH 4 to 5.5) and D-xylose ketol-isomerase (pH 7) at 298.15 K. The results show that by using the sol-mxDLVO model, protein solubility in polymer-salt solutions can be modeled in good agreement with the experimental data for both proteins considered. The sol-mxDLVO model can describe the non-monotonic course of protein solubility as a function of polymer concentration and salt concentration, previously not covered by state-of-the-art models. PMID:26579880

  9. Formation of globules and aggregates of DNA chains in DNA/polyethylene glycol/monovalent salt aqueous solutions

    OpenAIRE

    Kawakita, H.; Uneyama, T.; Kojima, M; Morishima, K.; Masubuchi, Y.; Watanabe, H.(Max-Planck-Institut für Kernphysik, 69117, Heidelberg, Germany)

    2009-01-01

    It has been known that giant DNA shows structural transitions in aqueous solutions under the existence of counterions and other polymers. However, the mechanism of these transitions has not been fully understood. In this study, we directly observed structures of probed (dye-labeled), dilute DNA chains in unprobed DNA/polyethylene glycol (PEG)/monovalent salt (NaCl) aqueous solutions with fluorescent microscopy to examine this mechanism. Specifically, we varied the PEG molecular weight and sal...

  10. Aggregation and stability of anisotropic charged clay colloids in aqueous medium in the presence of salt.

    Science.gov (United States)

    Ali, Samim; Bandyopadhyay, Ranjini

    2016-01-01

    Na-montmorillonite nanoclay is a colloid of layered mineral silicate. When dispersed in water, this mineral swells on absorption of water and exfoliates into platelets with electric double layers on their surfaces. Even at low particle concentration, the aqueous dispersion can exhibit a spontaneous ergodicity breaking phase transition from a free flowing liquid to nonequilibrium, kinetically arrested and disordered states such as gels and glasses. In an earlier publication [Applied Clay Science, 2015, 114, 8592], we showed that the stability of clay gels can be enhanced by adding a salt later to the clay dispersion prepared in deionized water, rather than by adding the clay mineral to a previously mixed salt solution. Here, we directly track the collapsing interface of sedimenting clay gels using an optical method and show that adding salt after dispersing the clay mineral does indeed result in more stable gels even in very dilute dispersions. These weak gels are seen to exhibit a transient collapse after a finite delay time, a phenomenon observed previously in depletion gels. The velocity of the collapse oscillates with the age of the sample. However, the average velocity of collapse increases with sample age up to a peak value before decreasing at higher ages. With increasing salt concentration, the delay time for transient collapse decreases, while the peak value of the collapsing velocity increases. Using ultrasound attenuation spectroscopy, rheometry and cryogenic scanning electron microscopy, we confirm that morphological changes of the gel network assembly, facilitated by thermal fluctuations, lead to the observed collapse phenomenon. Since clay minerals are used extensively in polymer nanocomposites, as rheological modifiers, stabilizers and gas absorbents, we believe that the results reported in this work are extremely useful for several practical applications and also for understanding geophysical phenomena such as the formation and stability of quicksand

  11. Mössbauer spectroscopic studies of frozen aqueous solutions of Fe3+ salts

    DEFF Research Database (Denmark)

    Mørup, Steen; Knudsen, J. E.; Nielsen, M. K.; Trumpy, Georg

    1976-01-01

    attributed to changes in the average separation between the iron ions. In the FeCl3–H2O system, it was found that homogeneous glasses are easily formed when the salt concentration is larger than 3.5 moles FeCl3 per 100 moles H2O. In more dilute samples, ice crystallizes during cooling, while the salt...... glass forming agents such as NO3 - , ClO4 - , and glycerol are also discussed. In some systems it was found that the states obtained after cooling depend critically on the cooling rate. The Journal of Chemical Physics is copyrighted by The American Institute of Physics....

  12. Hybrid Molten Salt Reactor (HMSR) System Study

    Energy Technology Data Exchange (ETDEWEB)

    Woolley, Robert D [PPPL; Miller, Laurence F [PPPL

    2014-04-01

    Can the hybrid system combination of (1) a critical fission Molten Salt Reactor (MSR) having a thermal spectrum and a high Conversion Ratio (CR) with (2) an external source of high energy neutrons provide an attractive solution to the world's expanding demand for energy? The present study indicates the answer is an emphatic yes.

  13. Self-consistent field theory investigation of the behavior of hyaluronic acid chains in aqueous salt solutions

    Science.gov (United States)

    Nogovitsin, E. A.; Budkov, Yu. A.

    2012-04-01

    In this work we continue to develop a field-theoretic methodology, which combines the technique of Gaussian equivalent representation for the calculation of functional integrals with the continuous Gaussian thread model of flexible polymers for solving statistical-mechanical problems of polyelectrolyte solutions. We present new analytic expressions for the osmotic pressure, the potential of mean force, and the monomer-monomer pair distribution function, and employ them to investigate the structural and thermodynamic quantities of the polyelectrolyte system. We demonstrate the applicability of the method for systems of polyelectrolyte chains in which the monomers interact via a Yukawa-type pair potential. As a specific example, the present work focuses on aqueous solutions of hyaluronic acid with added salts NaCl and CaCl2. Hyaluronic acid is a high molecular weight linear polysaccharide, which has a multitude of roles in biological tissues. We conclude that the effect of sodium chloride and calcium chloride on the osmotic properties of hyaluronic acid solutions can be accounted for by their contributions to the ionic strength. Nevertheless, the effects of coiling and self-association can be stimulated in solution by added salt.

  14. Interaction of molybdophosphates with palladium(II) salts in aqueous solutions

    International Nuclear Information System (INIS)

    The methods of electron and 31P NMR spectroscopies were used to study the interaction of H3PMo12O40 with H2PdCl4 or PdSO4 in aqueous solution at pH 3.0-4.5 and the ratio [Pd(II)]:[H3PMo12O40]=1:1. Palladium(II) remains in solution in the form of intensely colored hydroxo species and does not change the structure of the newly formed unsaturated heteropolymolybdates PMo11O397- and PMo9O349- as shown by NMR data. Heteropoly compounds precipitated from tetrabutylammonium or cesium salts were characterized using IR spectroscopy, differential dissolution and elemental analysis. It was found that the composition of a compound was affected by not only formation conditions in the solution but also the precipitant cation

  15. Sub-0.5 V Highly Stable Aqueous Salt Gated Metal Oxide Electronics

    Science.gov (United States)

    Park, Sungjun; Lee, Seyeong; Kim, Chang-Hyun; Lee, Ilseop; Lee, Won-June; Kim, Sohee; Lee, Byung-Geun; Jang, Jae-Hyung; Yoon, Myung-Han

    2015-08-01

    Recently, growing interest in implantable bionics and biochemical sensors spurred the research for developing non-conventional electronics with excellent device characteristics at low operation voltages and prolonged device stability under physiological conditions. Herein, we report high-performance aqueous electrolyte-gated thin-film transistors using a sol-gel amorphous metal oxide semiconductor and aqueous electrolyte dielectrics based on small ionic salts. The proper selection of channel material (i.e., indium-gallium-zinc-oxide) and precautious passivation of non-channel areas enabled the development of simple but highly stable metal oxide transistors manifested by low operation voltages within 0.5 V, high transconductance of ~1.0 mS, large current on-off ratios over 107, and fast inverter responses up to several hundred hertz without device degradation even in physiologically-relevant ionic solutions. In conjunction with excellent transistor characteristics, investigation of the electrochemical nature of the metal oxide-electrolyte interface may contribute to the development of a viable bio-electronic platform directly interfacing with biological entities in vivo.

  16. Line emissions from sonoluminescence in aqueous solutions of halide salts without noble gases

    International Nuclear Information System (INIS)

    Line emissions of trivalent terbium (Tb3+) ion were observed from single-bubble sonoluminescence (SL) in an aqueous solution of terbium chloride (TbCl3) that contained no noble gas. In addition, sodium (Na) lines were observed in multi-bubble SL in aqueous solutions of various halide salts that contained no noble gas. These observations show that the halide ions, such as Cl−, Br−, and I−, help for line emissions as the noble gases. The intensity of a line emission depends on both the chemical species produced by cavitation bubbles and the temperature of SL bubble that responds to the driving ultrasound pressure. With the increase of driving pressure, some line emissions attached to the continuous spectrum may become increasingly clear, while other line emissions gradually become indistinct. - Highlights: • Line emissions of Tb(III) ions were observed without the presence of noble gases. • The halide ions help to generate a line emission during sonoluminescence. • The intensity of a line emission mainly depends on the bubble's temperature. • The definition of a line emission is related to the temperature of caviation bubble and the kind of host liquid

  17. Sub-0.5 V Highly Stable Aqueous Salt Gated Metal Oxide Electronics.

    Science.gov (United States)

    Park, Sungjun; Lee, SeYeong; Kim, Chang-Hyun; Lee, Ilseop; Lee, Won-June; Kim, Sohee; Lee, Byung-Geun; Jang, Jae-Hyung; Yoon, Myung-Han

    2015-01-01

    Recently, growing interest in implantable bionics and biochemical sensors spurred the research for developing non-conventional electronics with excellent device characteristics at low operation voltages and prolonged device stability under physiological conditions. Herein, we report high-performance aqueous electrolyte-gated thin-film transistors using a sol-gel amorphous metal oxide semiconductor and aqueous electrolyte dielectrics based on small ionic salts. The proper selection of channel material (i.e., indium-gallium-zinc-oxide) and precautious passivation of non-channel areas enabled the development of simple but highly stable metal oxide transistors manifested by low operation voltages within 0.5 V, high transconductance of ~1.0 mS, large current on-off ratios over 10(7), and fast inverter responses up to several hundred hertz without device degradation even in physiologically-relevant ionic solutions. In conjunction with excellent transistor characteristics, investigation of the electrochemical nature of the metal oxide-electrolyte interface may contribute to the development of a viable bio-electronic platform directly interfacing with biological entities in vivo. PMID:26271456

  18. A stable liquid–liquid extraction system for clavulanic acid using polymer-based aqueous two-phase systems

    OpenAIRE

    Pereira, Jorge F. B.; Santos, Valéria Carvalho; Johansson, Hans-Olof; J. A. Teixeira; Pessoa Júnior, Adalberto

    2012-01-01

    The partitioning of Clavulanic Acid (CA) in a novel inexpensive and stable aqueous two-phase system (ATPS) composed by poly(ethylene glycol) (PEG) and sodium polyacrylate (NaPA) has been studied. The aqueous two-phase systems are formed by mixing both polymers with a salt (NaCl or Na2SO4) and an aqueous solution of CA. The stability of CA on the presence of both polymers was investigated and it was observed that these polymers do not degrade the biomolecule. The effect of PEG-molecular ...

  19. Effect of sodium phosphate salts on the thermodynamic properties of aqueous solutions of poly(ethylene oxide) 6000 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; Hosseini, Rahim; Jamehbozorg, Bahman [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of)

    2008-09-15

    Precise density, sound velocity, water activity, and phase diagram measurements have been carried out on polyethylene oxide (PEO) in aqueous solutions of sodium di-hydrogen phosphate, di-sodium hydrogen phosphate, and tri-sodium phosphate over a range of temperatures at atmospheric pressure. The experimental density and sound velocity data are used to calculate the apparent specific volume and isentropic compressibility as a function of temperature and concentration. It was found that both of the apparent specific volume and isentropic compressibility of PEO in aqueous solutions increase by increasing temperature and charge on the anion of electrolytes. The results show that the slope of constant water activity lines increased with increasing the temperature and charge on the anion of electrolytes and the vapour pressure depression for an aqueous (PEO + sodium phosphate) system is more than the sum of those for the corresponding binary solutions. Furthermore, the effect of temperature and type of anion of salt on the salting-out effect of polyethylene oxide by sodium phosphate salts has been studied.

  20. Magnetite Oxidation in Aqueous Systems

    OpenAIRE

    Templeton, John Andrew

    2008-01-01

    Magnetite, an iron oxide, is a possible candidate for in situ remediation of contaminated groundwater systems due to its oxidation/reduction potential for reduction of contaminants such as carbon tetrachloride. Little characterization and analysis has been done to describe the kinetics of magnetite transformation during oxidation. This work focuses on monitoring the concentrations of magnetite and one of its oxidation transformation products, maghemite, by the use of UV-Vis-NIR spectroscopy...

  1. Conductivity and Viscosity Measurements for Binary Lysozyme Chloride Aqueous Solution and Ternary Lysozyme-Salt-Water Solution

    CERN Document Server

    Buzatu, D; Buzatu, F D

    2004-01-01

    We use the conductimetric method, adequate to electrolytes, to determine the lysozyme charge in lys-water and ternary lys-salt-water systems. We measured also the viscosities for the above binary and ternary systems in the same conditions at pH$=4.5$ and T$=298$ K, measurements that allow us to see any effect of viscosity on cations mobilities and implicitly on the lysozyme charge. The method is illustrated for the lysozyme chloride aqueous solution system at 25$^o$ C, using the data reported here for pH$=4.5$ at 0.15, 0.6, 0.8, 1., 1.5, 2., 2.5, 3., 3.5 mM (mg/mL) lysozyme chloride concentrations. The method was also applied to ternary lys-salt-water systems in the same conditions at pH$=4.5$ and T$=25^o$ C. Ternary conductivities are reported for a mean concentration 0.6 mM of lysozyme chloride in all systems and a mean concentration 0.01, 0.025, 0.05, 0.1, 0.175, 0.2, 0.5, 0.7, 0.9, 1.2, 1.3 and 1.4 M for NaCl; 0.005, 0.01, 0.05, 0.1, 0.175, 0.2, 0.5, 0.7, 0.9, 1.2, 1.3, 1.4 and 1.5 M for KCl; 0.005, 0.01,...

  2. Phase diagrams of ionic liquids-based aqueous biphasic systems as a platform for extraction processes

    International Nuclear Information System (INIS)

    Highlights: • Novel ABS based in ionic liquids were determined as a platform for distinct extraction processes. • The effect of pH, IL cation core, alkyl side chain length, IL anion nature, and salt nature on the ABS formation was investigated. • The ability to form ABS increases with the pH and alkyl chain length for all systems studied. • The ILs cation core and anion nature effect on the ABS formation is dominated by the IL (hydrophobic/hydrophilic) nature. • The effect of the different salts depends of the ionic liquid nature and salt valency. - Abstract: In the past few years, ionic liquid-based aqueous biphasic systems have become the subject of considerable interest as a promising technique for the extraction and purification of several macro/biomolecules. Aiming at developing guidelines for more benign and efficient extraction processes, phase diagrams for aqueous biphasic systems composed of ionic liquids and inorganic/organic salts are here reported. Several combinations of ionic liquid families (imidazolium, pyridinium, phosphonium, quaternary ammonium and cholinium) and salts [potassium phosphate buffer (KH2PO4/K2HPO4 at pH 7), potassium citrate buffer (C6H5K3O7/C6H8O7 at pH 5, 6, 7 and 8) and potassium carbonate (K2CO3 at pH ∼13)] were evaluated to highlight the influence of the ionic liquid structure (cation core, anion and alkyl chain length), the pH and the salt nature on the formation of aqueous biphasic systems. The binodal curves and respective tie-lines reported for these systems were experimentally determined at (298 ± 1) K. In general, the ability to promote the aqueous biphasic systems formation increases with the pH and alkyl chain length. While the influence of the cation core and anion nature of the ionic liquids on their ability to form aqueous biphasic systems closely correlates with ionic liquids capacity to be hydrated by water, the effect of the different salts depends of the ionic liquid nature and salt valency

  3. Electrochemical activation of carbon cloth in aqueous inorganic salt solution for superior capacitive performance

    Science.gov (United States)

    Ye, Dong; Yu, Yao; Tang, Jie; Liu, Lin; Wu, Yue

    2016-05-01

    Carbon cloth (CC) is an inexpensive and highly conductive textile with excellent mechanical flexibility and strength; it holds great promise as an electrode material for flexible supercapacitors. However, pristine CC has such a low surface area and poor electrochemical activity that the energy storage capability is usually very poor. Herein, we report a green method, two-step electrochemical activation in an aqueous solution of inorganic salts, to significantly enhance the capacitance of CC for supercapacitor application. Micro-cracks, exfoliated carbon fiber shells, and oxygen-containing functional groups (OFGs) were introduced onto the surface of the carbon filament. This resulted in an enhancement of over two orders of magnitude in capacitance compared to that of the bare CC electrode, reaching up to a maximum areal capacitance of 505.5 mF cm-2 at the current density of 6 mA cm-2 in aqueous H2SO4 electrolyte. Electrochemical reduction of CC electrodes led to the removal of most electrochemically unstable surface OFGs, resulting in superior charging/discharging rate capability and excellent cycling stability. Although the activated CC electrode contained a high-level of surface oxygen functional groups (~15 at%), it still exhibited a remarkable charging-discharging rate capability, retaining ~88% of the capacitance when the charging rate increased from 6 to 48 mA cm-2. Moreover, the activated CC electrode exhibited excellent cycling stability with ~97% capacitance remaining after 10 000 cycles at a current density of 24 mA cm-2. A symmetrical supercapacitor based on the activated CC exhibited an ideal capacitive behavior and fast charge-discharge properties. Such a simple, environment-friendly, and cost-effective strategy to activate CC shows great potential in the fabrication of high-performance flexible supercapacitors.Carbon cloth (CC) is an inexpensive and highly conductive textile with excellent mechanical flexibility and strength; it holds great promise as

  4. Electrochemical activation of carbon cloth in aqueous inorganic salt solution for superior capacitive performance.

    Science.gov (United States)

    Ye, Dong; Yu, Yao; Tang, Jie; Liu, Lin; Wu, Yue

    2016-05-21

    Carbon cloth (CC) is an inexpensive and highly conductive textile with excellent mechanical flexibility and strength; it holds great promise as an electrode material for flexible supercapacitors. However, pristine CC has such a low surface area and poor electrochemical activity that the energy storage capability is usually very poor. Herein, we report a green method, two-step electrochemical activation in an aqueous solution of inorganic salts, to significantly enhance the capacitance of CC for supercapacitor application. Micro-cracks, exfoliated carbon fiber shells, and oxygen-containing functional groups (OFGs) were introduced onto the surface of the carbon filament. This resulted in an enhancement of over two orders of magnitude in capacitance compared to that of the bare CC electrode, reaching up to a maximum areal capacitance of 505.5 mF cm(-2) at the current density of 6 mA cm(-2) in aqueous H2SO4 electrolyte. Electrochemical reduction of CC electrodes led to the removal of most electrochemically unstable surface OFGs, resulting in superior charging/discharging rate capability and excellent cycling stability. Although the activated CC electrode contained a high-level of surface oxygen functional groups (∼15 at%), it still exhibited a remarkable charging-discharging rate capability, retaining ∼88% of the capacitance when the charging rate increased from 6 to 48 mA cm(-2). Moreover, the activated CC electrode exhibited excellent cycling stability with ∼97% capacitance remaining after 10 000 cycles at a current density of 24 mA cm(-2). A symmetrical supercapacitor based on the activated CC exhibited an ideal capacitive behavior and fast charge-discharge properties. Such a simple, environment-friendly, and cost-effective strategy to activate CC shows great potential in the fabrication of high-performance flexible supercapacitors. PMID:27141910

  5. The salting-out effect and phase separation in aqueous solutions of tri-sodium citrate and 1-butyl-3-methylimidazolium bromide

    Energy Technology Data Exchange (ETDEWEB)

    Sadeghi, Rahmat, E-mail: rsadeghi@uok.ac.i [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of); Golabiazar, Roonak [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of); Shekaari, Hemayat [Department of Chemistry, Faculty of Science, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of)

    2010-04-15

    The aim of this work is to obtain further evidence about the salting-out effect produced by the addition of tri-sodium citrate to aqueous solutions of water miscible ionic liquid 1-butyl-3-methylimidazolium bromide ([C{sub 4}mim][Br]) by evaluating the effect of tri-sodium citrate on the thermodynamic properties of aqueous solutions of this ionic liquid. Experimental measurements of density and sound velocity at different temperatures ranging from (288.15 to 308.15) K, the refractive index at 308.15 K and the liquid-liquid phase diagram at different temperatures ranging from (288.15 to 338.15) K for aqueous solutions containing 1-butyl-3-methylimidazolium bromide ([C{sub 4}mim][Br]) and tri-sodium citrate (Na{sub 3}Cit) are taken. The apparent molar volume of transfer of [C{sub 4}mim][Br] from water to aqueous solutions of Na{sub 3}Cit have positive values and it increases by increasing salt molality. Although at high IL molality, the apparent molar isentropic compressibility shows similar behaviour with that of the apparent molar volume. However at low concentrations of IL, the apparent molar isentropic compressibility of transfer of [C{sub 4}mim][Br] from water to aqueous solutions of Na{sub 3}Cit have negative values. The effects of temperature and the addition of Na{sub 3}Cit and [C{sub 4}mim][Br] on the liquid-liquid phase diagram of the investigated system have been studied. It was found that an increase in temperature caused the expansion of the one-phase region. The presence of Na{sub 3}Cit triggers a salting-out effect, leading to significant upward shifts of the liquid-liquid de-mixing temperatures of the system. The effect of temperature on the phase-forming ability in the system investigated has been studied based on a salting-out coefficient obtained from fitting the binodal values to a Setschenow-type equation for each temperature. Based on cloud point values, the energetics of the clouding process have been estimated and it was found that both of

  6. The salting-out effect and phase separation in aqueous solutions of tri-sodium citrate and 1-butyl-3-methylimidazolium bromide

    International Nuclear Information System (INIS)

    The aim of this work is to obtain further evidence about the salting-out effect produced by the addition of tri-sodium citrate to aqueous solutions of water miscible ionic liquid 1-butyl-3-methylimidazolium bromide ([C4mim][Br]) by evaluating the effect of tri-sodium citrate on the thermodynamic properties of aqueous solutions of this ionic liquid. Experimental measurements of density and sound velocity at different temperatures ranging from (288.15 to 308.15) K, the refractive index at 308.15 K and the liquid-liquid phase diagram at different temperatures ranging from (288.15 to 338.15) K for aqueous solutions containing 1-butyl-3-methylimidazolium bromide ([C4mim][Br]) and tri-sodium citrate (Na3Cit) are taken. The apparent molar volume of transfer of [C4mim][Br] from water to aqueous solutions of Na3Cit have positive values and it increases by increasing salt molality. Although at high IL molality, the apparent molar isentropic compressibility shows similar behaviour with that of the apparent molar volume. However at low concentrations of IL, the apparent molar isentropic compressibility of transfer of [C4mim][Br] from water to aqueous solutions of Na3Cit have negative values. The effects of temperature and the addition of Na3Cit and [C4mim][Br] on the liquid-liquid phase diagram of the investigated system have been studied. It was found that an increase in temperature caused the expansion of the one-phase region. The presence of Na3Cit triggers a salting-out effect, leading to significant upward shifts of the liquid-liquid de-mixing temperatures of the system. The effect of temperature on the phase-forming ability in the system investigated has been studied based on a salting-out coefficient obtained from fitting the binodal values to a Setschenow-type equation for each temperature. Based on cloud point values, the energetics of the clouding process have been estimated and it was found that both of entropy and enthalpy are the driving forces for biphasic

  7. Salting-out of methane in the aqueous solutions of urea and sarcosine

    Indian Academy of Sciences (India)

    M K Dixit; Anupam Chatterjee; B L Tembe

    2016-04-01

    Hydrophobic association and solvation of methane molecules in aqueous solutions of urea and sarcosine (sa) have been studied using MD simulations. The potentials of mean force (PMFs) between methane molecules in water, water-sa, water-urea and water-urea-sa mixtures show an enhancement of methane association on the addition of these osmolytes. These observations are well supported by calculation of equilibrium constants. Calculation of thermodynamic parameters shows that the association of methane is stabilized by entropy and favored by enthalpy. The hydrophobic solvation of methane is stabilized by enthalpy and destabilized by entropy. The calculated solvation free energies of methane in these mixtures show that methane is less soluble in the mixtures of urea and sarcosine than in water. The solubility is the least in the water-urea-sa mixture. Analysis of distributions of solvent and co-solvent around methane suggests that the local densities of both urea and sarcosine are diminished around the methane in the mixtures of these osmolytes. The selective reduction of both urea and sarcosine from methane surface suggests that both urea and sarcosine push methane molecules towards water and increase the interaction between methane molecules i.e., salting-out of methane.

  8. Application of salting-out effect equation to modelling of liquid-liquid distribution systems

    International Nuclear Information System (INIS)

    Physicochemical interpretation of salting-out is reviewed and effects of the medium on liquid-liquid distribution equilibria are described by two non-specific parameters of salting-out agents: total concentration of species in the aqueous phase and water activity. Thus extraction of a given constituent in various media can be forecasted with few data. Different uranyl and technetium (VII) extraction systems are analyzed to show the potentiality of the method. Coextraction of nitric acid and uranyl nitrate by tributyl phosphate is used to show the possibility of modelling complex distribution systems in industrial conditions

  9. A low-risk aqueous lithium salt blanket for engineering test reactors

    International Nuclear Information System (INIS)

    A simple blanket concept is proposed based on 1-3 wt.% lithium dissolved as a salt in low temperature (80 degrees C) and low pressure (0.1 MPa) water. This concept can provide, for example, a 0.5 tritium breeding ratio with 60% steel structure and 70% coverage. The use of neutron multipliers, other structural materials (especially zirconium alloys), higher coverage and higher lithium salt concentrations allows tritium breeding ratios over unity if necessary. Other advantages of this concept include the simple shield-like geometry, substantial structural volume for mechanical strength, excellent heat transfer ability of water coolant, efficient neutron and gamma shielding through the combination of high-Z structure and low-Z water, and conventional tritium recovery and control technology. This concept could initially provide the shielding needs for an engineering test reactor and later, by the addition of lithium salt and tritium recovery systems, also provide tritium breeding. This staged operation and liquid breeder/coolant allows control over the tritium inventory in the device without machine disassembly. 14 refs

  10. Viscosities of oxalic acid and its salts in water and binary aqueous mixtures of tetrahydrofuran at different temperatures

    Indian Academy of Sciences (India)

    M L Parmar; M K Guleria

    2005-07-01

    Relative viscosities for the solutions of oxalic acid and its salts, viz. ammonium oxalate, sodium oxalate and potassium oxalate, at different concentrations have been determined in water and in binary aqueous mixtures of tetrahydrofuran (THF) [5, 10, 15 and 20% by weight of THF] at 298.15 K, and in water and in 5% (w/w) THF + water at five different temperatures. The data have been evaluated using the Jones-Dole equation and the obtained parameters have been interpreted in terms of solute-solute and solute-solvent interactions. The activation parameters of viscous flow have been obtained which depicts the mechanism of viscous flow. The oxalic acid and its salts behave as structure breakers in water and in binary aqueous mixtures of THF.

  11. Electronic Tongue for Qualitative Analysis of Aqueous Solutions of Salts Using Thick-film Technology and Metal Electrodes

    Directory of Open Access Journals (Sweden)

    Juan Soto

    2006-09-01

    Full Text Available An electronic tongue for the qualitative analysis of aqueous solutions of salts hasbeen developed. The following set of electrodes was used: RuO2, Ag, and Cu in thick-filmtechnology and Au, Pb, Zn and Ni as small bars of the corresponding metal. The response ofthe designed “electronic tongue” was tested on a family of samples containing pure salt andcomplex mixtures. The electrodes were used as potentiometric un-specific sensors and thee.m.f. of each electrode in contact with a certain aqueous solution was used as input signalfor a PCA analysis. The study showed that the set of electrodes were capable to discriminatebetween aqueous solutions of salts basically by their different content in anions and cations(the anions SO42-, Cl-, PO4H2-, CO3H-, NO3- and cations Na+ and K+ were studied. In orderto better analyze the basis for the discrimination power shown by the electronic tongue, aquantitative analysis was also envisaged. A fair estimation of the concentrations of thedifferent ions in the solutions studied appeared to be possible using this electronic tonguedesign.Keywords:

  12. Investigation into aqueous solutions of lanthanum (3) and scandium (3) salts using 139La and 45Sc NMR method

    International Nuclear Information System (INIS)

    139La and 45Sc NMR method has been used to study composition and structure of lanthanum (3) and scandium (3) coordination sphere in aqueous solutions in respect to concentration of dissolved salt and nature of (NO3-, Cl-, ClO4-) anion. Lanthanum and scandium are shown to form intraspherical complexes both with nitrate- and with perchlorate anions. Chloride-ion able to complexing with Sc3+ ions in aqueous solutions coordinates to La3+ ions only in solutions with large excess of Cl- anions (Cl-:La3+ > 17.6 at lanthanum (3) concentration equal to 0.40 g-ion/l). Equilibrium between aquocomplexes with different coordination number N-nine and eight is stated to exist in aqueous solutions of lanthanum chloride, octaaquolanthanum (3) prevailing in concentrated solutions

  13. SANS from Salt-Free Aqueous Solutions of Hydrophilic and Highly Charged Star-Branched Polyelectrolytes

    Directory of Open Access Journals (Sweden)

    François Boué

    2016-06-01

    Full Text Available Scattering functions of sodium sulfonated polystyrene (NaPSS star-branched polyelectrolytes with high sulfonation degrees were measured from their salt-free aqueous solutions, using the Small Angle Neutron Scattering (SANS technique. Whatever the concentration c, they display two maxima. The first, of abscissa q1*, is related to a position order between star cores and scales as q1* ∝ c1/3. The second, of abscissa q2*, is also observed in the scattering function of a semi-dilute solution of NaPSS linear polyelectrolytes. In the dilute regime (c < c*, non-overlapping stars, peak abscissa does not depend on concentration c and is just an intramolecular characteristic associated with the electrostatic repulsion between arms of the same star. In the semi-dilute regime, due to the star interpenetration, the scattering function – through the peak position, reflects repulsion between arms of the same star or of different stars. The c threshold between these distinct c-dependencies of q2* in the dilute and semi-dilute regimes is estimated as c*. Just as simple is the measurement of the geometrical radius R of the star obtained from the q1* value at c* through the relation 2R = 2π/q1*. By considering NaPSS stars of the same functionality with different degrees of polymerization per arm Na, we find R scaling linearly with Na, suggesting an elongated average conformation of the arms. This is in agreement with theoretical predictions and simulations. Meanwhile the value of q2* measured in the dilute regime does not allow any inhomogeneous counterion distribution inside the stars to be revealed.

  14. High voltage AC/AC electrochemical capacitor operating at low temperature in salt aqueous electrolyte

    Science.gov (United States)

    Abbas, Qamar; Béguin, François

    2016-06-01

    We demonstrate that an activated carbon (AC)-based electrochemical capacitor implementing aqueous lithium sulfate electrolyte in 7:3 vol:vol water/methanol mixture can operate down to -40 °C with good electrochemical performance. Three-electrode cell investigations show that the faradaic contributions related with hydrogen chemisorption in the negative AC electrode are thermodynamically unfavored at -40 °C, enabling the system to work as a typical electrical double-layer (EDL) capacitor. After prolonged floating of the AC/AC capacitor at 1.6 V and -40°C, the capacitance, equivalent series resistance and efficiency remain constant, demonstrating the absence of ageing related with side redox reactions at this temperature. Interestingly, when temperature is increased back to 24 °C, the redox behavior due to hydrogen storage reappears and the system behaves as a freshly prepared one.

  15. Chain dimensions in free and immobilized brush states of polysulfobetaine in aqueous solution at various salt concentrations

    Energy Technology Data Exchange (ETDEWEB)

    Terayama, Y; Arita, H; Ishikawa, T; Takahara, A [Graduate School of Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0385 (Japan); Kikuchi, M; Mitamura, K; Kobayashi, M [JST, ERATO Takahara Soft Interfaces Project, 744 Motooka, Nishi-ku, Fukuoka 819-0385 (Japan); Yamada, N L, E-mail: takahara@cstf.kyushu-u.ac.jp [Neutron Science Laboratory, High Energy Accelerator Research Organization, 1-1 Oho, Tsukuba, Ibaraki 305-0801 (Japan)

    2011-01-01

    The chain dimensions of free and immobilized polysulfobetaine in aqueous solution at various salt concentrations were investigated by size-exclusion chromatography with multiangle light scattering and neutron reflectivity measurement, respectively. The dependence of the z-average mean square radius of gyration ({sub z}{sup 1/2}) on the weight-average molecular weight (M{sub w}) of free poly(3-(N-2-methacryloyloxyethyl-N,N-dimethyl)ammonatopropanesulfo-nate) (MAPS) in aqueous solution at salt concentrations of 74, 100, 200, and 500 mM was described by the perturbed wormlike chain model using the chain stiffness parameter {lambda}{sup -1} the molar mass per unit contour length ML, and the excluded volume effect B. B increased from 0 to 1.8 nm with increasing salt concentration to 500 mM due to the screening of attractive electrostatic interaction between ammonium cations and sulfonyl anions by salt ions. The swollen structure of the poly(MAPS) brush in D{sub 2}O changed from a shrunken state to a relatively extended state with increasing salt concentration from 0 to 500 mM NaCl/D{sub 2}O solution. The thickness of the swollen poly(MAPS) brush in 500 mM NaCl/D{sub 2}O was 9.0 times greater than 2{sub z}{sup 1/2} of free poly(MAPS) due to high osmotic pressure generated by the excluded volume effect of densely grafted polymer chains.

  16. Monodisperse PEGylated spheres: an aqueous colloidal model system.

    Science.gov (United States)

    Ulama, Jeanette; Zackrisson Oskolkova, Malin; Bergenholtz, Johan

    2014-03-01

    Fluorinated core-shell spheres have been synthesized using a novel semibatch emulsion polymerization protocol employing slow feeding of the initiator. The synthesis results in aqueous dispersions of highly monodisperse spheres bearing a well-defined poly(ethylene glycol) graft (PEGylation). Measurements are consistent with the synthesis achieving a high grafting density that moreover consists of a single PEG layer with the polymer significantly elongated beyond its radius of gyration in bulk. The fluorination of the core of the particles confers a low index of refraction such that the particles can be refractive index matched in water through addition of relatively small amounts of a cosolvent, which enables the use of optical and laser-based methods for studies of concentrated systems. The systems exhibit an extreme stability in NaCl solutions, but attractions among particles can be introduced by addition of other salts, in which case aggregation is shown to be reversible. The PEGylated sphere dispersions are expected to be ideally suited as model systems for studies of the effect of PEG-mediated interactions on, for instance, structure, dynamics, phase behavior, and rheology. PMID:24533774

  17. Advanced Aqueous Separation Systems for Actinide Partitioning

    Energy Technology Data Exchange (ETDEWEB)

    Nash, Ken [Washington State Univ., Pullman, WA (United States); Martin, Leigh [Idaho National Lab. (INL), Idaho Falls, ID (United States); Lumetta, Gregg [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2015-04-02

    One of the most challenging aspects of advanced processing of used nuclear fuel is the separation of transplutonium actinides from fission product lanthanides. This separation is essential if actinide transmutation options are to be pursued in advanced fuel cycles, as lanthanides compete with actinides for neutrons in both thermal and fast reactors, thus limiting efficiency. The separation is difficult because the chemistry of Am3+ and Cm3+ is nearly identical to that of the trivalent lanthanides (Ln3+). The prior literature teaches that two approaches offer the greatest probability of devising a successful group separation process based on aqueous processes: 1) the application of complexing agents containing ligand donor atoms that are softer than oxygen (N, S, Cl-) or 2) changing the oxidation state of Am to the IV, V, or VI state to increase the essential differences between Am and lanthanide chemistry (an approach utilized in the PUREX process to selectively remove Pu4+ and UO22+ from fission products). The latter approach offers the additional benefit of enabling a separation of Am from Cm, as Cm(III) is resistant to oxidation and so can easily be made to follow the lanthanides. The fundamental limitations of these approaches are that 1) the soft(er) donor atoms that interact more strongly with actinide cations than lanthanides form substantially weaker bonds than oxygen atoms, thus necessitating modification of extraction conditions for adequate phase transfer efficiency, 2) soft donor reagents have been seen to suffer slow phase transfer kinetics and hydro-/radiolytic stability limitations and 3) the upper oxidation states of Am are all moderately strong oxidants, hence of only transient stability in media representative of conventional aqueous separations systems. There are examples in the literature of both approaches having been described. However, it is not clear at present that any extant process is sufficiently robust for application at the scale

  18. Correlation of aqueous solubility of salts of benzylamine with experimentally and theoretically derived parameters. A multivariate data analysis approach

    DEFF Research Database (Denmark)

    Parshad, Henrik; Frydenvang, Karla Andrea; Liljefors, Tommy;

    2002-01-01

    .0 were intrinsic dissolution rate, intrinsic solubility of the unionized acids (S(0)), Hansch's hydrophobic parameter, Charton's steric parameter and molecular weight (MW). Statistically good models for predicting solubility of a selected test set were obtained by using simple models consisting of a few......Twenty two salts of benzylamine and p-substituted benzoic acids were prepared and characterized. The p-substituent was varied with regard to electronic, hydrophobic, and steric effects as well as hydrogen bonding potential. A multivariate data analysis was used to describe the relationship between...... the aqueous solubility of the salts and experimentally determined physicochemical parameters and theoretically derived molecular descriptors. The model, based on all descriptors, gave R(2)=0.86 and Q(2)=0.72. The most significant descriptors exhibiting VIP (variance of importance) values above 1...

  19. The production of HTR-fuel kernels by microwave hardening of aqueous metal-salt-resin droplets

    International Nuclear Information System (INIS)

    The construction and function of the microwave equipment for the hardening of free falling salt-resin-droplets, the preparation of solutions, their treatment and conditioning of the hardening process, the appearance and properties of the hardened ''green'' kernels and the transformation of ''green'' kernels of HTR-fuel kernels, i.e. sintered UO2-particles are described. With a suitable microwave equipment it is possible to harden aqueous droplets containing metal-salts (e.g. uranylnitrate), resorcinol and formaldehyde. The hardening occurs while the mentioned droplets are falling under gravity. These particles are suitable for the production of HTR-fuel kernels, e.g. high density UO2-particles. The entire process has the advantage of minimising the process specific waste. (author)

  20. Nicotine aqueous solutions: pH-measurements and salting-out effects - analysis of the effective Gibbs energies of hydration and ionic strengths of the solutions

    Directory of Open Access Journals (Sweden)

    Grozdanić Nikola D.

    2014-01-01

    Full Text Available This work is a continuation of our previous studies on the phase demixing - salting-out effects - in aqueous nicotine solutions. Thus, pH measurements were carried out allowing a brief analysis of the existing hydrogen bond interactions. Salting-out effects - the related experimental cloud point shifts - provoked by the addition of two inorganic salts, potassium nitrate and sodium sulfate, which were not studied so far, were determined. Analysis of the current and our previously reported salting-out/or salting-in phenomena in nicotine aqueous solutions was performed. In this respect, five studied salts were included: four inorganic salts (sodium chloride, potassium nitrate, sodium sulfate and sodium phosphate (Na3PO4 and ionic liquid 1-ethyl-3-methylimidazolium ethyl sulfate ([C2mim][EtSO4] or ECOENG212®. Based on the pH measurements the effective Gibbs energies of hydration and ionic strengths of the respective ternary solutions were calculated and plotted against the related cloud-point shifts caused by the addition of the salts. For the studied salts, the results and diagram obtained within this work may be used to predict the cloud-points shifts, based on the related quantities of the salts added and/or the molar Gibbs energies of hydration and/or ionic strengths requested in each case. [Projekat Ministarstva nauke Republike Srbije, br. 172063

  1. Efficient adsorption of both methyl orange and chromium from their aqueous mixtures using a quaternary ammonium salt modified chitosan magnetic composite adsorbent.

    Science.gov (United States)

    Li, Kun; Li, Pei; Cai, Jun; Xiao, Shoujun; Yang, Hu; Li, Aimin

    2016-07-01

    A quaternary ammonium salt modified chitosan magnetic composite adsorbent (CS-CTA-MCM) was prepared by combination of Fe3O4 nanoparticles. Various techniques were used to characterize the molecular structure, surface morphology, and magnetic feature of this composite adsorbent. CS-CTA-MCM was employed for the removal of Cr(VI) and methyl orange (MO), an anionic dye, from water in respective single and binary systems. Compared with chitosan magnetic adsorbent (CS-MCM) without modification, CS-CTA-MCM shows evidently improved adsorption capacities for both pollutants ascribed to the additional quaternary ammonium salt groups. Based on the adsorption equilibrium study, MO bears more affinity to CS-CTA-MCM than Cr(VI) causing a considerable extent of preferential adsorption of dye over metal ions in their aqueous mixture. However, at weak acidic solutions, Cr(VI) adsorption is evidently improved due to more efficient Cr(VI) forms, i.e. dichromate and monovalent chromate, binding to this chitosan-based adsorbent. Thus chromium could be efficient removal together with MO at suitable pH conditions. The adsorption isotherms and kinetics indicate that adsorptions of Cr(VI) and MO by CS-CTA-MCM both follow a homogeneous monolayer chemisorption process. This magnetic adsorbent after saturated adsorption could be rapidly separated from water and easily regenerated using dilute NaOH aqueous solutions then virtually reused with little adsorption capacity loss. PMID:27060639

  2. Soft X-ray absorption spectra of aqueous salt solutions with highly charged cations in liquid microjets

    Energy Technology Data Exchange (ETDEWEB)

    Schwartz, Craig P.; Uejio, Janel S.; Duffin, Andrew M.; Drisdell, Walter S.; Smith, Jared D.; Saykally, Richard J.

    2010-03-11

    X-ray absorption spectra of 1M aqueous solutions of indium (III) chloride, yttrium (III) bromide, lanthanum (III) chloride, tin (IV) chloride and chromium (III) chloride have been measured at the oxygen K-edge. Relatively minor changes are observed in the spectra compared to that of pure water. SnCl{sub 4} and CrCl{sub 3} exhibit a new onset feature which is attributed to formation of hydroxide or other complex molecules in the solution. At higher energy, only relatively minor, but salt-specific changes in the spectra occur. The small magnitude of the observed spectral changes is ascribed to offsetting perturbations by the cations and anions.

  3. Rheological and kinetic study of the ultrasonic degradation of locust bean gum in aqueous saline and salt-free solutions.

    Science.gov (United States)

    Li, Ruoshi; Feke, Donald L

    2015-11-01

    The ultrasonic degradation of locust bean gum (LBG) in aqueous solutions has been studied at 25°C for ultrasonication times up to 120 min. Although LBG is not a polyelectrolyte, the degradation extent and kinetics were found to be somewhat sensitive to the ionic conditions in solution, and this is attributed to changes in molecular conformation that can occur in different salt environments. Ultrasonic degradation was tracked by rheological measurements that lead to the determination of intrinsic viscosity for the LBG molecules. A kinetic model was also developed and successfully applied to characterize and predict the degradation results. PMID:26186852

  4. Separation and determination of chloramphenicol in sewage using a small molecules-salt aqueous two-phase flotation system coupled with HPLC%小分子双水相浮选高效液相色谱法测定污水中痕量氯霉素

    Institute of Scientific and Technical Information of China (English)

    姚以亮; 关卫省

    2011-01-01

    用乙醇/磷酸氢二钾双水相体系浮选污水中的氯霉索,通过对盐的质量分数、有机溶剂的体积、气体流速和浮选时间的选择和优化,在理想条件下,氯霉素的平均浮选效率可以达到94%.该方法用于河水和鱼塘水样品中氯霉素的检测,检出限为0.5 ng/mL,加标回收率为89.44%~100.16%,相对标准偏差RSD为1.1%~2.1%,适用于污水中痕量氯霉素的分离/富集及分析测定.%C2H5OH/K2HPO4 two-phase aqueous system was used to floate CAP in sewage. By selecting and optimizing mass percentage of salt, volume of organic solvent, gas flow rate and flotation time, under the optimum conditions,the average floatation efficiency was up to 94% . The method used to detect CAP in the samples of river and pond water, the detection limit was 0. 5 ng/mL, the relative recovery was 89. 44% ~ 100. 16% with relative standard deviation RSD = 1. 1%~ 2. 1% . The method is applicable to analyze the trace CAP in swage.

  5. Palladium-Catalyzed Heck Coupling Reaction of Aryl Bromides in Aqueous Media Using Tetrahydropyrimidinium Salts as Carbene Ligands

    Directory of Open Access Journals (Sweden)

    İsmail Özdemir

    2010-01-01

    Full Text Available An efficient and stereoselective catalytic system for the Heck cross coupling reaction using novel 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium salts (1, LHX and Pd(OAc2 loading has been reported. The palladium complexes derived from the salts 1a-f prepared in situ exhibit good catalytic activity in the Heck coupling reaction of aryl bromides under mild conditions.

  6. Thermal Characterization of Molten Salt Systems

    Energy Technology Data Exchange (ETDEWEB)

    Toni Y. Gutknecht; Guy L. Fredrickson

    2011-09-01

    The phase stability of molten salts in an electrorefiner (ER) may be adversely affected by the buildup of sodium, fission products, and transuranics in the electrolyte. Potential situations that need to be avoided are the following: (1) salt freezing due to an unexpected change in the liquidus temperature, (2) phase separation or non-homogeneity of the molten salt due to the precipitation of solids or formation of immiscible liquids, and (3) any mechanism that can result in the separation and concentration of fissile elements from the molten salt. Any of these situations would result in an off-normal condition outside the established safety basis for electrorefiner (ER) operations. The stability (and homogeneity) of the phases can potentially be monitored through the thermal characterization of the salts, which can be a function of impurity concentration. This report describes the experimental results of typical salts compositions, which consist of chlorides of potassium, lithium, strontium, samarium, praseodymium, lanthanum, barium, cerium, cesium, neodymium, sodium and gadolinium chlorides as a surrogate for both uranium and plutonium, used for the processing of used nuclear fuels.

  7. Thermodynamic study of aqueous solutions of polyelectrolytes of low and medium charge density without added salt by direct measurement of osmotic pressure

    International Nuclear Information System (INIS)

    A special block osmometer has been constructed and applied to a systematic study of poly (vinyl alcohol and vinyl sulphate ester) (PVS) sodium salts in dilute and moderately concentrated salt free aqueous solutions. In order to avoid surely ionic contamination all parts of the equipment that can contact with the polyelectrolyte solutions were made of different kinds of plastics and glass. The pressure range spans from (50 to 1.3 . 105) Pa. The measuring system was found to be appropriate for determination of the molar mass of water soluble polymers, too. Above a certain analytical density of dissociable groups (ADDG) an ion size dependent transition was observed on the reduced osmotic pressure vs. concentration curves. The analysis of the osmotic pressure data has clearly revealed that the dependence of the degree of dissociation on ADDG calculated at zero polyelectrolyte concentration contradicts to 'ion condensation' theory. With increasing polyelectrolyte concentration the degree of dissociation decreased rather steeply but at very low concentrations sharp maximums appeared due either to the change in conformation of these charged macromolecules, or formation of dynamic clusters induced by salting out of neutral parts of the macromolecules by the ionized groups. The applicability of the scaling concept as well as the many possible ways of characterization of non-ideality of polyelectrolyte solutions will be discussed in detail.

  8. Analysis of Direct Samples of Early Solar System Aqueous Fluids

    Science.gov (United States)

    Zolensky, Michael E.; Bodnar, R J.; Fedele, L.; Yurimoto,H.; Itoh, S.; Fries, M.; Steele, A.

    2012-01-01

    Over the past three decades we have become increasingly aware of the fundamental importance of water, and aqueous alteration, on primitive solar-system bodies. Some carbonaceous and ordinary chondrites have been altered by interactions with liquid water within the first 10 million years after formation of their parent asteroids. Millimeter to centimeter-sized aggregates of purple halite containing aqueous fluid inclusions were found in the matrix of two freshly-fallen brecciated H chondrite falls, Monahans (1998, hereafter simply "Monahans") (H5) and Zag (H3-6) (Zolensky et al., 1999; Whitby et al., 2000; Bogard et al., 2001) In order to understand origin and evolution of the aqueous fluids inside these inclusions we much measure the actual fluid composition, and also learn the O and H isotopic composition of the water. It has taken a decade for laboratory analytical techniques to catch up to these particular nanomole-sized aqueous samples. We have recently been successful in (1) measuring the isotopic composition of H and O in the water in a few fluid inclusions from the Zag and Monahans halite, (2) mineralogical characterization of the solid mineral phases associated with the aqueous fluids within the halite, and (3) the first minor element analyses of the fluid itself. A Cameca ims-1270 equipped with a cryo-sample-stage of Hokkaido University was specially prepared for the O and H isotopic measurements. The cryo-sample-stage (Techno. I. S. Corp.) was cooled down to c.a. -190 C using liquid nitrogen at which the aqueous fluid in inclusions was frozen. We excavated the salt crystal surfaces to expose the frozen fluids using a 15 keV Cs+ beam and measured negative secondary ions. The secondary ions from deep craters of approximately 10 m in depth emitted stably but the intensities changed gradually during measurement cycles because of shifting states of charge compensation, resulting in rather poor reproducibility of multiple measurements of standard fluid

  9. Ice VII from aqueous salt solutions: From a glass to a crystal with broken H-bonds.

    Science.gov (United States)

    Klotz, S; Komatsu, K; Pietrucci, F; Kagi, H; Ludl, A-A; Machida, S; Hattori, T; Sano-Furukawa, A; Bove, L E

    2016-01-01

    It has been known for decades that certain aqueous salt solutions of LiCl and LiBr readily form glasses when cooled to below ≈160 K. This fact has recently been exploited to produce a « salty » high-pressure ice form: When the glass is compressed at low temperatures to pressures higher than 4 GPa and subsequently warmed, it crystallizes into ice VII with the ionic species trapped inside the ice lattice. Here we report the extreme limit of salt incorporation into ice VII, using high pressure neutron diffraction and molecular dynamics simulations. We show that high-pressure crystallisation of aqueous solutions of LiCl∙RH2O and LiBr∙RH2O with R = 5.6 leads to solids with strongly expanded volume, a destruction of the hydrogen-bond network with an isotropic distribution of water-dipole moments, as well as a crystal-to-amorphous transition on decompression. This highly unusual behaviour constitutes an interesting pathway from a glass to a crystal where translational periodicity is restored but the rotational degrees of freedom remaining completely random. PMID:27562476

  10. Adsorption and reduction: combined effect of polyaniline emeraldine salt for removal of Cr(VI) from aqueous medium

    Indian Academy of Sciences (India)

    PURNIMA BARUAH; DEBAJYOTI MAHANTA

    2016-06-01

    In this study, we have reported the removal of Cr(VI) ions by polyaniline (PANI) particles from aqueous medium. PANI in its emeraldine salt (ES) form can interact with Cr(VI), which is present as HCrO$^{−}_4$ in two ways. The adsorption of HCrO$^{−}_4$ ions due to the electrostatic interaction between partially positively charged PANI backbone and Cr(VI) anions causes the major portion of Cr(VI) removal and a small portion of Cr(VI) is reduced to Cr(III) by PANI (ES). The adsorption follows Langmuir adsorption isotherm and second-order kinetic model. It is observed that the removal of Cr(VI) is negligibly effected by the presence of other anions in the aqueous medium. The adsorption capacity of PANI (ES) is found to be 123 mg g$^{−1}$, which is very high compared to activated carbonbased materials. The adsorbed anions can be desorbed by converting PANI emeraldine salt (ES) to PANI emeraldinebase (EB). The EB form of PANI can be converted into ES form by treating with acid, which can be reused as adsorbent. It is important to note that the PANI (ES) is oxidized by HCrO$^{−}_4$ ions which decrease the hydrophilicity of thesurface of PANI particles. This causes the decrease in adsorption capacity of recycled PANI.

  11. OSMOTIC COEFFICIENTS, SOLUBILITIES, AND DELIQUESCENCE RELATIONS IN MIXED AQUEOUS SALT SOLUTIONS AT ELEVATED TEMPERATURE

    International Nuclear Information System (INIS)

    While thermodynamic properties of pure aqueous electrolytes are relatively well known at ambient temperature, there are far fewer data for binary systems extending to elevated temperatures and high concentrations. There is no general theoretically sound basis for prediction of the temperature dependence of ionic activities, and consequently temperature extrapolations based on ambient temperature data and empirical equations are uncertain and require empirical verification. Thermodynamic properties of mixed brines in a wide range of concentrations would enhance the understanding and precise modeling of the effects of deliquescence of initially dry solids in humid air in geological environments and in modeling the composition of waters during heating, cooling, evaporation or condensation processes. These conditions are of interest in the analysis of waters on metal surfaces at the proposed radioactive waste repository at Yucca Mountain, Nevada. The results obtained in this project will be useful for modeling the long-term evolution of the chemical environment, and this in turn is useful for the analysis of the corrosion of waste packages. In particular, there are few reliable experimental data available on the relationship between relative humidity and composition that reveals the eutonic points of the mixtures and the mixture deliquescence RH. The deliquescence RH for multicomponent mixtures is lower than that of pure component or binary solutions, but is not easy to predict quantitatively since the solutions are highly nonideal. In this work we used the ORNL low-temperature and high-temperature isopiestic facilities, capable of precise measurements of vapor pressure between ambient temperature and 250 C for determination of not only osmotic coefficients, but also solubilities and deliquescence points of aqueous mixed solutions in a range of temperatures. In addition to standard solutions of CaCl2, LiCl, and NaCl used as references, precise direct

  12. An Overview of Liquid Fluoride Salt Heat Transport Systems

    Energy Technology Data Exchange (ETDEWEB)

    Holcomb, David Eugene [ORNL; Cetiner, Sacit M [ORNL

    2010-09-01

    Heat transport is central to all thermal-based forms of electricity generation. The ever increasing demand for higher thermal efficiency necessitates power generation cycles transitioning to progressively higher temperatures. Similarly, the desire to provide direct thermal coupling between heat sources and higher temperature chemical processes provides the underlying incentive to move toward higher temperature heat transfer loops. As the system temperature rises, the available materials and technology choices become progressively more limited. Superficially, fluoride salts at {approx}700 C resemble water at room temperature being optically transparent and having similar heat capacity, roughly three times the viscosity, and about twice the density. Fluoride salts are a leading candidate heat-transport material at high temperatures. Fluoride salts have been extensively used in specialized industrial processes for decades, yet they have not entered widespread deployment for general heat transport purposes. This report does not provide an exhaustive screening of potential heat transfer media and other high temperature liquids such as alkali metal carbonate eutectics or chloride salts may have economic or technological advantages. A particular advantage of fluoride salts is that the technology for their use is relatively mature as they were extensively studied during the 1940s-1970s as part of the U.S. Atomic Energy Commission's program to develop molten salt reactors (MSRs). However, the instrumentation, components, and practices for use of fluoride salts are not yet developed sufficiently for commercial implementation. This report provides an overview of the current understanding of the technologies involved in liquid salt heat transport (LSHT) along with providing references to the more detailed primary information resources. Much of the information presented here derives from the earlier MSR program. However, technology has evolved over the intervening years

  13. Phosphate-dependent root system architecture responses to salt stress

    KAUST Repository

    Kawa, Dorota

    2016-05-20

    Nutrient availability and salinity of the soil affect growth and development of plant roots. Here, we describe how phosphate availability affects root system architecture (RSA) of Arabidopsis and how phosphate levels modulate responses of the root to salt stress. Phosphate (Pi) starvation reduced main root length and increased the number of lateral roots of Arabidopsis Col-0 seedlings. In combination with salt, low Pi dampened the inhibiting effect of mild salt stress (75mM) on all measured RSA components. At higher NaCl concentrations, the Pi deprivation response prevailed over the salt stress only for lateral root elongation. The Pi deprivation response of lateral roots appeared to be oppositely affected by abscisic acid (ABA) signaling compared to the salt stress response. Natural variation in the response to the combination treatment of salt and Pi starvation within 330 Arabidopsis accessions could be grouped into four response patterns. When exposed to double stress, in general lateral roots prioritized responses to salt, while the effect on main root traits was additive. Interestingly, these patterns were not identical for all accessions studied and multiple strategies to integrate the signals from Pi deprivation and salinity were identified. By Genome Wide Association Mapping (GWAS) 13 genomic loci were identified as putative factors integrating responses to salt stress and Pi starvation. From our experiments, we conclude that Pi starvation interferes with salt responses mainly at the level of lateral roots and that large natural variation exists in the available genetic repertoire of accessions to handle the combination of stresses.

  14. Impact of Deepwater Horizon Oil Contamination on the Aqueous Geochemistry of Salt Marsh Sediment/Seawater Microcosms

    Science.gov (United States)

    Rentschler, E. K.; Donahoe, R. J.

    2011-12-01

    On April 20th, 2010, the Deepwater Horizon oil drilling rig, located in the Gulf of Mexico about 41 miles off the Louisiana coast, exploded, burned for two days, and sank. Approximately 4.9 million gallons of crude oil were released and traveled with ocean currents to reach the coasts of Louisiana, Mississippi, Alabama, and Florida. Previous studies have primarily considered the direct impact of oil and dispersant contamination on coastal ecosystems, but have not examined the potential impact of the accident on the inorganic geochemistry of coastal waters and sediments. In this study, microcosm experiments were conducted to determine how oil contamination will affect the concentration and distribution of trace elements in a salt marsh environment. Uncontaminated sediment and seawater, collected from a salt marsh at Bayou la Batre, Alabama, were measured into jars and spiked with 500 ppm MC-252 oil. Twenty jars, including duplicates and both sterile and non-sterile controls, were placed on a shaker table at 100 rpm. The jars were sacrificed at predetermined time intervals (0 h, 6 h, 12 h, 24 h, 48 h, 7 d, and 14 d), and the aqueous samples prepared for analysis by ICP-OES and IC. The pH for the water in the time series experiment ranged from 7.16 to 8.06. Seawater alkalinity was measured at 83.07 mg CaCO3/L. ICP-OES data show variations in aqueous element concentrations over the 14 day microcosm experiment. Significant positive correlations (>0.75) were found for the following pairs of elements: calcium and magnesium, calcium and sodium, magnesium and sodium, silica and boron, beryllium and boron, iron and silica, manganese and silica, boron and manganese, arsenic and nickel, beryllium and selenium, beryllium and zinc, copper and chloride, bromide and sulfate. Aqueous iron concentrations were highly correlated with solution pH. The presence of iron oxide and clays in the sediment indicates a potential for adsorption of trace elements sourced from the environment and

  15. Effect of plasticizer on surface of free films prepared from aqueous solutions of salts of cationic polymers with different plasticizers

    Science.gov (United States)

    Bajdik, János; Fehér, Máté; Pintye-Hódi, Klára

    2007-06-01

    Acquisition of a more detailed understanding of all technological processes is currently a relevant tendency in pharmaceutical technology and hence in industry. A knowledge of film formation from dispersion of polymers is very important during the coating of solid dosage forms. This process and the structure of the film can be influenced by different additives. In the present study, taste-masking films were prepared from aqueous citric acid solutions of a cationic polymer (Eudragit ® E PO) with various hydrophilic plasticizers (glycerol, propylene glycol and different poly(ethylene glycols)). The mechanical properties, film thickness, wetting properties and surface free energy of the free films were studied. The aim was to evaluate the properties of surface of free films to predict the arrangement of macromolecules in films formed from aqueous solutions of salts of cationic polymers. A high molecular weight of the plasticizer decreased the work of deformation. The surface free energy and the polarity were highest for the film without plasticizer; the hydrophilic additives decreased these parameters. The direction of the change in polarity (a hydrophilic component caused a decrease in the polarity) was unexpected. It can be explained by the change in orientation of the macromolecules, a hydrophobic surface being formed. Examination of the mechanical properties and film thickness can furnish additional results towards a knowledge of film formation by this not frequently applied type of polymer from aqueous solution.

  16. Modeling of Dielectric Properties of Aqueous Salt Solutions with an Equation of State

    DEFF Research Database (Denmark)

    Maribo-Mogensen, Bjørn; Kontogeorgis, Georgios; Thomsen, Kaj

    2013-01-01

    , been ignored in relation to thermodynamic modeling, and authors have either neglected the effect of salts on permittivity or used empirical correlations fitted to the measured static permittivity, leading to an overestimation of the reduction in the thermodynamic static permittivity. We present a new...... in the electrical field surrounding ions. Kinetic depolarization may explain 25–75% of the observed decrease in the permittivity of solutions containing salts, but since this is a dynamic property, this effect should not be included in the thermodynamic modeling of electrolytes. Kinetic depolarization has, however...... methodology for obtaining the static permittivity over wide ranges of temperatures, pressures, and compositions for use within an equation of state for mixed solvents containing salts. The static permittivity is calculated from a new extension of the framework developed by Onsager, Kirkwood, and Fröhlich...

  17. The effect of sulphates on partitioning of pectinases in aqueous two-phase systems

    Directory of Open Access Journals (Sweden)

    Antov Mirjana G.

    2004-01-01

    Full Text Available The effect of various sulphate salts on the partitioning of endo-pectinase and exo-pectinase in aqueous two-phase systems, composed of polyethylene glycol and dextran, was studied. Presence of ammonium sulphate and sodium sulphate at concentration 15 mmol/l in the system polyethylene glycol 4000/crude dextran, at tie-line length 7.44%, increased partition coefficient of endo-pectinase 1.25 and 1.2 fold, respectively. Ammonium sulphate at 15 mmol/l and sodium sulphate at 5 mmol/l enhanced partition coefficient for exo-pectinase for about 60% in comparison to the system without salts. Addition of magnesium and sodium sulphate to a final concentration of 0.3 mmol/l in the system containing polyethylene glycol 6000/dextran 500 000, at tie-line length 6.26%, increased the partition coefficient of endo activity for 95% and 32%, respectively. Both salts at the same concentration increased partition coefficient of exo activity 1.5 and 3 times, respectively, in comparison to the system without salts.

  18. Salt movements within the Central European basin system

    Energy Technology Data Exchange (ETDEWEB)

    Maystrenko, Yuriy; Bayer, Ulf; Scheck-Wenderoth [GeoForschungsZentrum (GFZ), Potsdam (Germany); Littke, Ralf [RWTH Aachen (Germany). Lehrstuhl fuer Geologie, Geochemie und Lagerstaetten des Erdoels und der Kohle

    2010-04-15

    Evolution of salt structures in relation to tectonic events within central part of the Central European Basin System is described by summarizing results which have been obtained and published in frame of the research project DFG-SPP 1135. These results illustrate main phases of salt tectonics within the basin system from the Triassic to present day. During the Buntsandstein and Muschelkalk, extension triggered raft tectonics and salt movements within the Ems Trough, the Glueckstadt and the Horn Grabens. The next phase of salt movements occurred in response to a Middle-Late Keuper regional extensional event which was strongest within the Triassic depocenters of the Central European Basin System, such as the Horn Graben, the Glueckstadt Graben, the Ems and the Rheinsberg Troughs. Regional erosion truncated the study area during the Late Jurassic-Early Cretaceous time. The magnitude of Late Jurassic-Early Cretaceous erosion is declining towards southern margin of the basin system where a dextral transtensional regime was established in the Lower Saxony Basin and neighboring areas during the Late Jurassic-Early Cretaceous. The late Early Cretaceous-early Late Cretaceous is characterized by a relative tectonic quiescence without strong salt movements. The Late Cretaceous-Early Cenozoic inversion provocated renewed salt movements, causing the thick-skinned salt tectonics along the Elbe Fault System and the thin-skinned character of salt movements towards the north from the area of strain localisation. Post-inversion Cenozoic subsidence was accompanied by salt movements, related either to diapiric rise due to regional shortening and/or to local almost E-W directed extension. (orig.)

  19. Ion Pairing in Aqueous Lithium Salt Solutions with Monovalent and Divalent Counter-Anions

    Czech Academy of Sciences Publication Activity Database

    Pluhařová, Eva; Mason, Philip E.; Jungwirth, Pavel

    2013-01-01

    Roč. 117, č. 46 (2013), s. 11766-11773. ISSN 1089-5639 R&D Projects: GA MŠk LH12001 Grant ostatní: MŠMT(CZ) LM2010005 Institutional support: RVO:61388963 Keywords : lithium * aqueous solution * neutron scattering * molecular dynamics * polarizability Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.775, year: 2013

  20. Salt dependent stability of stearic acid Langmuir-Blodgett films exposed to aqueous electrolytes

    NARCIS (Netherlands)

    Kumar, Naveen; Wang, Lei; Siretanu, Igor; Duits, Michel; Mugele, Frieder

    2013-01-01

    We use contact angle goniometry, imaging ellipsometry, and atomic force microscopy to study the stability and wettability of Langmuir–Blodgett (LB) monolayers of stearic acid on silica substrates, upon drying and exposure to aqueous solutions of varying salinity. The influences of Ca2+ and Na+ ions

  1. Cathodic treatment of the Si-SiO2 system in salt melts

    International Nuclear Information System (INIS)

    This paper studies metal ion transport in SiO2 dielectric layers during their cathodic treatment in salt melts. The preparation of the samples is described. It is shown that an important special feature of cathodic treatments of the silicon-thermal oxide system in salt melts is the formation of a new solid phase at the bottom of the micropores which leads to blocking of the current during subsequent anodic polarization. This is a difference relative to aqueous electrolyes, where cathodic treatment involving hydrogen evolution promotes corrosion of the micropores. The C-V characteristics of the electrolyte-dielectric-semiconductor systems that had been subjected to cathodic treatment in melts are examined at room temperature in 0.0 N KC1. The results are shown

  2. Conformation dynamics and polarization effect of α,α-trehalose in a vacuum and in aqueous and salt solutions.

    Science.gov (United States)

    Kan, Zigui; Yan, Xiufen; Ma, Jing

    2015-03-01

    Conformational changes of α,α-trehalose in a vacuum, water, and 0-20 wt % NaCl solutions were investigated by means of molecular dynamics (MD) simulations at different levels of density function theory (DFT) and with fixed-charge nonpolarizable and variable-charge force fields (FFs), respectively. The relative thermodynamic stability of trehalose is enhanced by the formation of intercycle and/or intracycle hydrogen bonds, but some thermodynamically unfavorable structures can be sampled in the DFT-based ab initio MD simulation. The polarization effects of polar trehalose molecule in aqueous and NaCl solutions were studied by a series of MD simulations with both the conventional nonpolarizable and polarizable force field models. In the polarizable model, the partial charges of trehalose were updated every 2 ps using DFT calculations and fused with the other FF parameters for the energy calculation and MD simulation. Around the trehalose, water molecules located in an asymmetry model and trehalose have a stronger tendency to bind with water molecules than Na(+) and Cl(-) ions. When the trehalose concentration is increased from 3.26 to 6.31 wt % in salt aqueous solution, the two trehalose molecules periodically approach each other in a nearly anhydrate state and leave a way to keep the favorable hydration structure with the mean trehalose-trehalose distance of 8.6 Å. The similarity between the solvated dimer packing styles (shoulder-by-shoulder or head-to-head) and crystal stacking can be used to make an extrapolation to higher sugar concentrations and to rationalize the bioprotection function of trehalose in high salt concentration. PMID:25506668

  3. Activity coefficients of ferrocenium iodide in aqueous-organic salt solutions

    International Nuclear Information System (INIS)

    Values of electrode potentials were obtained by the method of potentiometric titration at 298.2 K, the standard values of emf and unified activity coefficients of ferrocenium iodide in water-acetone and water-ethanol solvents of different salt composition being calculated. It is shown that interaction of ferrocenium (Fc+) with iodide can occur with formation of two forms of complexes, i.e. [Fc+I-] and [Fc+I2]-

  4. Sorption of thorium by alkylammonium salts of iso- and heteropolyacids of transition metals from aqueous solutions

    International Nuclear Information System (INIS)

    Results of investigations of thorium extraction from aqueous solutions by coprecipitation with water-repellent compounds, forming in direct interaction of 12-molybdophosphate heteropolyacid (HPA) with alkyltrimethylammoniumchloride, depending on the aqueous phase acidity are presented. It is established that degree of thorium extraction increases with an increase in the pH value and at transition to solutions with more diluted HPA. Thorium in hydrochloric acid media is extracted at a higher acidity of the aqueous phase in comparison with sulfuric acid media at the same concentration of HPA in the solution which is equal to 3.1x10-3 mol/l. Interaction of thorium with water-repellent precipitations proceeds due to processes of Th complexino. with HPA or HPA decomposition products. Data on infrared spectroscopic investigations of the composition of the water-repellent precipitations obtained under different conditions are presented. It is shown that the differences in the character of thorium distribution between precipitate and solution depend on the changes in the solid phase composition

  5. Synthesis of β-Hydroxy Sulfides via Thiolysis of Epoxides Using S-Alkylisothiouronium Salts as Thiol Equivalents in Basic Aqueous Medium

    Institute of Scientific and Technical Information of China (English)

    ZHU,Jirang; LI,Ridong; GE,Zemei; CHENG,Tieming; LI,Runtao

    2009-01-01

    S-Alkylisothiouronium salt as a nontoxic,odorless and simply operational alternative of thiol was reacted with different kinds of epoxides in basic aqueous medium at room temperature affording the β-hydroxy sulfides with high regioselectivity in excellent yields.

  6. Comparison of colorimetric methods for the quantification of model proteins in aqueous two-phase systems.

    Science.gov (United States)

    Glyk, Anna; Heinisch, Sandra L; Scheper, Thomas; Beutel, Sascha

    2015-05-15

    In the current study, the quantification of different model proteins in the presence of typical aqueous two-phase system components was investigated by using the Bradford and bicinchoninic acid (BCA) assays. Each phase-forming component above 1 and 5 wt% had considerable effects on the protein quantification in both assays, respectively, resulting in diminished protein recoveries/absorption values by increasing poly(ethylene glycol) (PEG)/salt concentration and PEG molecular weight. Therefore, a convenient dilution of both components (up to 1 and 5 wt%) before protein quantification is recommended in both assays, respectively, where the BCA assay is favored in comparison with the Bradford assay. PMID:25684109

  7. Thermo-responsive properties driven by hydrogen bonding in aqueous cationic gemini surfactant systems.

    Science.gov (United States)

    Wei, Xi-Lian; Han, Chuan-Hong; Geng, Pei-Pei; Chen, Xiao-Xiao; Guo, Yan; Liu, Jie; Sun, De-Zhi; Zhang, Jun-Hong; Yu, Meng-Jiao

    2016-02-01

    A series of unexpected thermo-responsive phenomena were discovered in an aqueous solution of the cationic gemini surfactant, 2-hydroxypropyl-1,3-bis(alkyldimethylammonium chloride) (n-3(OH)-n(2Cl), n = 14, 16), in the presence of an inorganic salt. The viscosity change trend for the 14-3(OH)-14(2Cl) system was investigated in the 20-40 °C temperature range. As the temperature increased, the viscosity of the solution first decreased to a minimum point corresponding to 27 °C, and then increased until a maximum was reached, after which the viscosity decreased again. In the 16-3(OH)-16(2Cl) system, the gelling temperature (T(gel)) and viscosity changes upon heating were similar to those in the 14-3(OH)-14(2Cl) system above 27 °C. The reversible conversion of elastic hydrogel to wormlike micelles in the aqueous solution of the 16-3(OH)-16(2Cl) system in the presence of an inorganic salt was observed at relatively low temperatures. Various techniques were used to study and verify the phase-transition processes in these systems, including rheological measurements, cryogenic transmission electron microscopy (cryo-TEM), electric conductivity, and differential scanning calorimetry. The abovementioned phenomena were explained by the formation and destruction of intermolecular hydrogen bonds, and the transition mechanisms of the aggregates were analyzed accordingly. PMID:26659081

  8. Radiation protection of vitamins in aqueous systems

    International Nuclear Information System (INIS)

    A study of the radiation induced decomposition of the B-group vitamins has been carried out in aqueous media at room temperature as well as in rigid matrices at low temperature. The detailed results on the effect of glucose and oxygen as protective additives at the different temperatures are presented in the case of Thiamine (Vitamin B1). Comparative data are given on the extent of decomposition of this and other vitamins of the B-group at room temperature and at 193 K. The importance of these results in connection with the radiation sterilization of pharmaceutical preparations is indicated. (author)

  9. Extraction of Biomolecules Using Phosphonium-Based Ionic Liquids + K3PO4 Aqueous Biphasic Systems

    Directory of Open Access Journals (Sweden)

    Cláudia L. S. Louros

    2010-04-01

    Full Text Available Aqueous biphasic systems (ABS provide an alternative and efficient approach for the extraction, recovery and purification of biomolecules through their partitioning between two liquid aqueous phases. In this work, the ability of hydrophilic phosphonium-based ionic liquids (ILs to form ABS with aqueous K3PO4 solutions was evaluated for the first time. Ternary phase diagrams, and respective tie-lines and tie-lines length, formed by distinct phosphonium-based ILs, water, and K3PO4 at 298 K, were measured and are reported. The studied phosphonium-based ILs have shown to be more effective in promoting ABS compared to the imidazolium-based counterparts with similar anions. Moreover, the extractive capability of such systems was assessed for distinct biomolecules (including amino acids, food colourants and alkaloids. Densities and viscosities of both aqueous phases, at the mass fraction compositions used for the biomolecules extraction, were also determined. The evaluated IL-based ABS have been shown to be prospective extraction media, particularly for hydrophobic biomolecules, with several advantages over conventional polymer-inorganic salt ABS.

  10. Phase behaviour of tertiary recovery sulfonates - petroleum fractions - aqueous systems

    Energy Technology Data Exchange (ETDEWEB)

    Ghoniem, S.A.; Darwish, T.A.; Salamah, A.O.

    1988-02-01

    The phase behaviour of tertiary recovery sulfonates having commercial names TRS-10, TRS-16 and TRS-40 with aqueous phase and light petroleum fractions (non polar kerosene and gasoline) was studied at 20, 40 and 60/sup 0/C. The adopted pseudo components of the ternary diagram are hydrocarbon, surfactant and aqueous phase. The aqueous phase was composed of bidistilled water in addition to different proportions of pure alcohols and sodium chloride. The tested alcohols included methanol, ethanol, iso-propanol, n-butanol and n-pentanol. Thus, the best alcohol type and concentration in addition to optimum salinity, which correspond to maximum single phase region, were established for each surfactant at the various tested temperatures. It was shown that higher the affinity of the tested surfactant for hydrocarbon phase, the greater is the solubility of the corresponding optimum co-surfactant in water. The variation of optimum alcohol concentration with temperature, the effect of salt on the single phase region and the effect of hydrocarbon phase on the observed phenomena were discussed and found to agree with the previously established theories.

  11. 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.

  12. Effect of salt identity on the phase diagram for a globularprotein in aqueous electrolyte solution

    Energy Technology Data Exchange (ETDEWEB)

    Bostrom, Mathias; Tavares, Frederico W.; Ninham, Barry W.; Prausnitz, John M.

    2006-02-22

    Monte Carlo simulations are used to establish the potential of mean force between two globular proteins in an aqueous electrolyte solution. This potential includes nonelectrostatic contributions arising from dispersion forces first, between the globular proteins, and second, between ions in solution and between each ion and the globular protein. These latter contributions are missing from standard models. The potential of mean force, obtained from simulation, is fitted to an analytic equation. Using our analytic potential of mean force and Barker-Henderson perturbation theory, we obtain phase diagrams for lysozyme solutions that include stable and metastable fluid-fluid and solid-fluid phases when the electrolyte is 0.2 M NaSCN or NaI or NaCl. The nature of the electrolyte has a significant effect on the phase diagram.

  13. Purification of C-phycocyanin from Spirulina platensis in aqueous two-phase systems using an experimental design

    OpenAIRE

    Francine Silva Antelo; Jorge Alberto Vieira Costa; Susana Juliano Kalil

    2015-01-01

    C-phycocyanin from Spirulina platensis was purified in aqueous two-phase systems (ATPS) of polyethylene glycol (PEG)/potassium phosphate, varying the molar mass of the PEG. Results using a full factorial design showed that an increase in the concentration of salt and decrease in the concentration of PEG caused an increment in the purification factor for all the ATPS studied. Optimization of the conditions of the purification was studied using a central composite rotatable design for each mola...

  14. Assessment of the combined approach of N-alkylation and salt formation to enhance aqueous solubility of tertiary amines using bupivacaine as a model drug

    DEFF Research Database (Denmark)

    Nielsen, Anders Bach; Frydenvang, Karla Andrea; Liljefors, Tommy;

    2005-01-01

    tertiary amine (up to a factor of 3200 at pH 8). A moderate reduction in solubility with increasing length of the alkyl chain was observed for the iodide salts of the N-alkylated bupivacaine derivatives. In case of the N-methyl-bupivacaine derivative variation of the counterion had a significant impact......Quaternary prodrug types of poorly water-soluble tertiary amines have been shown to exhibit significantly enhanced solubilities as compared to the parent amine. In the present study the combined effect of N-alkylation and salt formation to enhance aqueous solubility of tertiary amines have been...... investigated using bupivacaine as a model compound. X-ray structure analyses of selected salts were included to investigate the potential existence of correlations between salt solubility and crystal packing modes. Alkyl groups were methyl, ethyl, propyl, and butyl and the derivatives were isolated...

  15. A system for separation, salt encapsulation and disposal of lava-like fuel-containing mass from the 4-th block Chernobyl nuclear power station in salt mines

    International Nuclear Information System (INIS)

    The offered here system of separations, salt capsulation and disposal LFCM in salt mines completely corresponds to these principles. Basic elements of the system are: the technological scheme of separation LFCM on activity and isotope structure with selection of valuable components by means of enrichment of mineral ore dressing; the technological scheme of conditioning LFCM with use artificial salt structures - salt capsules; disposal LFCM in spent space of salt mines; storehouse of high-active LFCM in salt formations

  16. Protons and Hydroxide Ions in Aqueous Systems.

    Science.gov (United States)

    Agmon, Noam; Bakker, Huib J; Campen, R Kramer; Henchman, Richard H; Pohl, Peter; Roke, Sylvie; Thämer, Martin; Hassanali, Ali

    2016-07-13

    Understanding the structure and dynamics of water's constituent ions, proton and hydroxide, has been a subject of numerous experimental and theoretical studies over the last century. Besides their obvious importance in acid-base chemistry, these ions play an important role in numerous applications ranging from enzyme catalysis to environmental chemistry. Despite a long history of research, many fundamental issues regarding their properties continue to be an active area of research. Here, we provide a review of the experimental and theoretical advances made in the last several decades in understanding the structure, dynamics, and transport of the proton and hydroxide ions in different aqueous environments, ranging from water clusters to the bulk liquid and its interfaces with hydrophobic surfaces. The propensity of these ions to accumulate at hydrophobic surfaces has been a subject of intense debate, and we highlight the open issues and challenges in this area. Biological applications reviewed include proton transport along the hydration layer of various membranes and through channel proteins, problems that are at the core of cellular bioenergetics. PMID:27314430

  17. Ultrasonic-assisted synthesis of aqueous CdTe/CdS QDs in salt water bath heating

    International Nuclear Information System (INIS)

    Highlights: • Ultrasonic promotes formation of crystal nucleus and QDs were synthesized in 0.5 h. • The new heating method provides a PLQY of up to 97.13%. • The synthesis mechanism of the core shell structure of the CdTe/CdS QDs was inferred. • The preparation method was efficient, simple and clean. - Abstract: A novel simple method for fast and efficient synthesis of aqueous CdTe/CdS quantum dots (QDs) with core–shell structure was developed by using salt water bath heating with the ultrasonic-assisted technique in this paper. The formation of crystal nucleus was promoted by ultrasonic and CdTe/CdS QDs with blue fluorescence were synthesized only in 0.5 h. The heat source was bath heating in salt water solution at 60% NaCl and the heating temperature could reach 105 °C. The heating method solved the biggest drawback of low photoluminescence quantum yield (PLQY) of ordinal bath heating in water. The preparation was cheap, simple and had less pollution to the environment. The properties of the CdTe/CdS QDs were thoroughly investigated by ultraviolet–visible (UV–vis), photoluminescence (PL), transmission electron microscope (TEM), laser size analysis, fourier transform infrared spectra (FTIR), X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDS). Different CdTe/CdS QDs with core shell structure were efficiently synthesized and the maximum PLQY could reach 97.13% when refluxing at 105 °C for 2 h. These QDs exhibited uniform dispersity, high fluorescence intensity, good optical property and long life of fluorescent. The synthesis mechanism of the core shell structure of the QDs was inferred that the Cd2+ might coordinate with sulfur (S) as well as thiol propionate (–SCH2CH2COO−1) to constitute two relatively thick compound layers on the QDs surface as passive shells

  18. Cellulose aerogels prepared from an aqueous zinc chloride salt hydrate melt.

    Science.gov (United States)

    Schestakow, Maria; Karadagli, Ilknur; Ratke, Lorenz

    2016-02-10

    Monolithic cellulose aerogels are prepared using a salt hydrate melt based on cheap zinc chloride tetrahydrate (ZnCl2·4H2O) that can be washed out of the wet gel-body by using common solvents such as water, ethanol, isopropanol or acetone. Cellulose aerogels with concentrations of 1-5 wt.% cellulose were produced. These aerogels are characterized with respect to shrinkage, density and surface area as well as mechanical properties and micro-structure via SEM. Cellulose aerogels regenerated in acetone show a specific surface area of around 340 m(2)g(-1) being 60% higher than those regenerated in water. The onset of irreversible plastic deformation under compressive load is around 0.8 MPa for acetone-regenerated aerogels and thus a factor of two larger compared to ethanol regenerated ones. The Young's modulus depends almost linearly on the cellulose concentration which is observed for all regenerative fluids with the exception of water. The results achieved are presented in light of the polarity and ability of solvation of ZnCl2·4H2O in the regenerative fluids used. PMID:26686174

  19. Photoemission spectra of aqueous solutions of salts from many-body perturbation theory

    Science.gov (United States)

    Gaiduk, Alex P.; Skone, Jonathan H.; Govoni, Marco; Galli, Giulia

    The computational design of electrode materials for energy conversion and storage processes requires an accurate description of the energy levels of the electrolyte and of electrolyte/electrode interfaces. Conventional density-functional approximations are in general not well suited for this task as they yield inaccurate orbital energies. Many-body perturbation theory (MBPT) predicts vertical ionization potentials and energy gaps in better agreement with experiments, providing the possibility for an accurate description of the electronic properties of electrolytes. We coupled ab initio molecular dynamics with MBPT calculations to investigate the photoemission spectra of a 1 M aqueous solution of NaCl. For the first time we were able to determine the absolute positions of the spectra peaks, with excellent agreement with experiments for both the solute and solvent peak positions. The best results were obtained using wavefunctions obtained from dielectric-dependent hybrid calculations as a starting point for MBPT. Work supported by DOE BES DE-SC0008938. Computer time provided by the Argonne Leadership Computing Facility through the INCITE program.

  20. Interfacial behavior of perchlorate versus chloride ions in saturated aqueous salt solutions

    Energy Technology Data Exchange (ETDEWEB)

    Ghosal, S; Kuo, I W; Baer, M D; Bluhm, H

    2009-04-14

    In recent years combination of theoretical and experimental work have presented a novel view of the aqueous interface wherein hard and/or multiply charged ions are excluded from the interface, but large polarizable anions show interfacial enhancement relative to the bulk. The observed trend in the propensity of anions to adsorb at the air/water interface appears to be reverse of the Hofmeister series for anions. This study focuses on experimental and theoretical examination of the partitioning behavior of perchlorate (ClO{sub 4}{sup -}) and chloride (Cl{sup -}) ions at the air/water interface. We have used ambient pressure X-ray photoelectron spectroscopy technique to directly probe the interfacial concentrations of ClO{sub 4}{sup -} and Cl{sup -} ions in sodium perchlorate and sodium chloride solutions, respectively. Experimental observations are compared with first principles molecular dynamics simulations. Both experimental and simulation results show enhancement of ClO{sub 4}{sup -} ion at the interface, compared with the absence of such enhancement in the case of Cl{sup -} ion. These observations are in agreement with the expected trend in the interfacial propensity of anions based on the Hofmeister series.

  1. Dissolution of nickel ferrite in aqueous solutions containing oxalic acid and ferrous salts

    International Nuclear Information System (INIS)

    The dissolution of nickel ferrite in oxalic acid and in ferrous oxalate-oxalic acid aqueous solution was studied. Nickel ferrite was synthesized by thermal decomposition of a mixed tartrate; the particles were shown to be coated with a thin ferric oxide layer. Dissolution takes place in two stages, the first one corresponding to the dissolution of the ferric oxide outer layer and the second one being the dissolution of Ni1.06Fe1.96O4. The kinetics of dissolution during this first stage is typical of ferric oxides: in oxalic acid, both a ligand-assisted and a redox mechanism operates, whereas in the presence of ferrous ions, redox catalysis leads to a faster dissolution. The rate dependence on both oxalic acid and on ferrous ion is described by the Langmuir-Hinshelwood equation. In the second stage, Langmuir-Hinshelwood kinetics also describes the dissolution of iron and nickel from nickel ferrite. It may be concluded that oxalic acid operates to dissolve iron, and the ensuing disruption of the solid framework accelerates the release of nickel

  2. 4-Hydroxyphenacyl Ammonium Salts: A Photoremovable Protecting Group for Amines in Aqueous Solutions.

    Science.gov (United States)

    Bownik, Iwona; Šebej, Peter; Literák, Jaromír; Heger, Dominik; Šimek, Zdeněk; Givens, Richard S; Klán, Petr

    2015-10-01

    Irradiation of N-protected p-hydroxyphenacyl (pHP) ammonium caged derivatives at 313 nm releases primary and secondary amines or ammonia in nearly quantitative yields via the photo-Favorskii reaction when conducted in acidic or neutral aqueous buffered media. The reaction efficiencies are strongly dependent on the pH with the most efficient and highest yields obtained when the pH of the media maintains the ammonium and p-hydroxyl groups as their conjugate acids. For example, the overall quantum yields of simple secondary amines release are 0.5 at acidic pH from 3.9 to 6.6 dropping to 0.1 at neutral pH 7.0 and 0.01 at pH 8.4. Speciation studies provide an acid-base profile that helps define the scope and limitations of the reaction. When the pKa of the ammonium group is lower than that of the phenolic hydroxyl group, as is the case for the α-amino-protected amino acids, the more acidic ammonium ion deprotonates as the media pH is changed from acidic toward neutral or basic, thus diminishing the leaving group ability of the amino group. This, in turn, lowers the propensity for the photo-Favorskii rearrangement reaction to occur and opens the reaction pathway to alternative competing photoreduction process. PMID:26373949

  3. Molten Chloride Salts for Heat Transfer in Nuclear Systems

    Science.gov (United States)

    Ambrosek, James Wallace

    2011-12-01

    A forced convection loop was designed and constructed to examine the thermal-hydraulic performance of molten KCl-MgCl2 (68-32 at %) salt for use in nuclear co-generation facilities. As part of this research, methods for prediction of the thermo-physical properties of salt mixtures for selection of the coolant salt were studied. In addition, corrosion studies of 10 different alloys were exposed to the KCl-MgCl2 to determine a suitable construction material for the loop. Using experimental data found in literature for unary and binary salt systems, models were found, or developed to extrapolate the available experimental data to unstudied salt systems. These property models were then used to investigate the thermo-physical properties of the LINO3-NaNO3-KNO 3-Ca(NO3), system used in solar energy applications. Using these models, the density, viscosity, adiabatic compressibility, thermal conductivity, heat capacity, and melting temperatures of higher order systems can be approximated. These models may be applied to other molten salt systems. Coupons of 10 different alloys were exposed to the chloride salt for 100 hours at 850°C was undertaken to help determine with which alloy to construct the loop. Of the alloys exposed, Haynes 230 had the least amount of weight loss per area. Nickel and Hastelloy N performed best based on maximum depth of attack. Inconel 625 and 718 had a nearly uniform depletion of Cr from the surface of the sample. All other alloys tested had depletion of Cr along the grain boundaries. The Nb in Inconel 625 and 718 changed the way the Cr is depleted in these alloys. Grain-boundary engineering (GBE) of Incoloy 800H improved the corrosion resistance (weight loss and maximum depth of attack) by nearly 50% as compared to the as-received Incoloy 800H sample. A high temperature pump, thermal flow meter, and pressure differential device was designed, constructed and tested for use in the loop, The heat transfer of the molten chloride salt was found to

  4. Specific Na+ and K+ Cation Effects on the Interfacial Water Molecules at the Air/Aqueous Salt Solution Interfaces Probed with Non-resonant Second Harmonic Generation (SHG)

    OpenAIRE

    Bian, Hong-tao; Feng, Ran-Ran; Guo, Yuan; Wang, Hong-fei

    2008-01-01

    Here we report the polarization dependent non-resonant second harmonic generation (SHG) measurement of the interfacial water molecules at the aqueous solution of the following salts: NaF, NaCl, NaBr, KF, KCl, and KBr. Through quantitative polarization analysis of the SHG data,the orientational parameter D value and the relative surface density of the interfacial water molecules at these aqueous solution surfaces were determined. From these results we found that addition of each of the six sal...

  5. "Water-in-salt" electrolytes enable the use of cost-effective aluminum current collectors for aqueous high-voltage batteries.

    Science.gov (United States)

    Kühnel, R-S; Reber, D; Remhof, A; Figi, R; Bleiner, D; Battaglia, C

    2016-08-16

    The extended electrochemical stability window offered by highly concentrated electrolytes allows the operation of aqueous batteries at voltages significantly above the thermodynamic stability limit of water, at which the stability of the current collector potentially limits the cell voltage. Here we report the observation of suppressed anodic dissolution of aluminum in "water-in-salt" electrolytes enabling roll-to-roll electrode fabrication for high-voltage aqueous lithium-ion batteries on cost-effective light-weight aluminum current collectors using established lithium-ion battery technology. PMID:27488137

  6. Tritium and excess heat generation during electrolysis of aqueous solutions of alkali salts with nickel cathode

    International Nuclear Information System (INIS)

    A number of open cell electrolysis experiments of the Mills and Kneizys type using Nickel as cathode, Pt wire as anode and aqueous solutions of carbonates of Potassium, Sodium and Lithium (natural and enriched) as electrolyte have been carried out in three different laboratories at Trombay. The cells were fabricated out of commercial dewar vacuum flasks. The difference in temperature at equilibrium between the operating cells and that of an identical dummy reference flask was measured to deduce excess heat. The cells were calibrated using resistance heaters. In all, studies have been carried out so far in 29 electrolytic cells with various electrolytes. In some cases a mixture of H2O and D2O was used. The cells were operated for a few weeks at a time and excess heat up to a maximum of 70% appears to be present in most cells when the input joule power is upto a watt or two. The current density was less than 40 mA/cm2. Electrolyte samples before and after electrolysis were analysed for tritium content after microdistillation to eliminate chemiluminescence effects. Samples from 18 out of 29 experiments analysed have indicated tritium levels varying in the region of 46 Bq/ml to 3390 Bq/ml. One cell with enriched Li2CO3 solution in H2O which was monitored continuously for over a month indicated that tritium generation is continuous. Although the highest amount of tritium produced so far was with a K2CO3 in 25% D2O cell, the generation of tritium in cells containing only H2O is a new finding. (author)

  7. Comparison of microenvironments of aqueous sodium dodecyl sulfate micelles in the presence of inorganic and organic salts: a time-resolved fluorescence anisotropy approach.

    Science.gov (United States)

    Dutt, G B

    2005-11-01

    Microenvironments of aqueous sodium dodecyl sulfate (SDS) micelles was examined in the presence of additives such as sodium chloride and p-toluidine hydrochloride (PTHC) by monitoring the fluorescence anisotropy decays of two hydrophobic probes, 2,5-dimethyl-1,4-dioxo-3,6-diphenylpyrrolo[3,4-c]pyrrole (DMDPP) and coumarin 6 (C6). It has been well-established that SDS micelles undergo a sphere-to-rod transition and that their mean hydrodynamic radius increases from 19 to 100 A upon the addition of 0.0-0.7 M NaCl at 298 K. A similar size and shape transition is induced by PTHC at concentrations that are 20 times lower compared to that of NaCl. This study was undertaken to find out how the microviscosity of the micelles is influenced under these circumstances. It was noticed that the microviscosity of the SDS/NaCl system increased by approximately 45%, whereas there was a less than 10% variation in the microviscosity of the SDS/PTHC system. The large increase in the microviscosity of the former system with salt concentration has been rationalized on the basis of the high concentration of sodium ions in the headgroup region of the micelles and their ability to strongly coordinate with the water present in this region, which decreases the mobility of the probe molecules. PMID:16262297

  8. Isotope effect of potassium in an aqueous/amalgam system

    International Nuclear Information System (INIS)

    The isotope fractionation of potassium in an aqueous (KOH)/amalgam system has been studied. Two types of isotope effects with opposite isotope enrichment directions were observed in the electrolysis of potassium from the aqueous into the amalgam phase under constant electrolytic potentials. It was found that the first isotope effect causing the light isotope enriched in the amalgam is related to the kinetic process of the mass transfer through the aqueous/amalgam interface, while the second one leading to the enrichment of the heavy isotope in the amalgam phase is produced by the isotope-exchange equilibrium. The temperature dependence of the equilibrium isotope effect was also investigated using single-stage and multi-stage techniques. It was observed that the equilibrium isotope effect increases as the temperature increases in the range of 293-371 K. An empirical equation was used to fit the variations of the isotope effects with temperature for potassium together with the other alkaline and alkaline earth metals studied in the same system. The origin of the equilibrium isotope fractionation in the electron-exchange system was discussed. Furthermore, the mass dependence of the separation coefficients of the alkaline and alkaline earth metals observed in aqueous/amalgam and ion-exchange systems were compared. At 293 K the equilibrium isotope separation coefficient for the 39K/41K isotopes in the amalgam system was determined as (5.6 ± 0.6).10-3. (author)

  9. Atomistic molecular dynamics simulations of the structure of symmetric Polyelectrolyte block copolymer micelle in salt-free aqueous solution

    Science.gov (United States)

    Chockalingam, Rajalakshmi; Natarajan, Upendra

    2014-03-01

    The structure of a symmetric polystyrene- b - poly(acrylic acid) (PS- b - PAA) micelle in salt-free aqueous solution as a function of degree-of-neutralization (or ionization, f) of the PAA is studied via explicit-atom-ion MD simulations, for the first time for a polyelectrolyte block copolymer in a polar solvent. Micelle size increases with fin agreement with experimental observations in literature, due to extension of PAA at higher ionization. Pair RDF's with respect to water oxygens show that corona-water interaction becomes stronger with f due to an increase in number density of carboxylate (COO-) groups on the chain. Water-PAA coordination (carboxylate O's) increases with ionization. H-bonding between PAA and water increases with f due to greater extent of corona-water affinity. With increase in f, atom and counter-ion ρ profiles confirm extension of corona blocks and micelle existing in the ``osmotic regime,'' and a decrease in scattering peak intensity, in agreement with neutron scattering experiments and mean-field theory in literature. Inter-chain distance in PS core is found to decrease with ionization. Macromolecular Simulation and Modeling Laboratory, Dept. of Chemical Engineering, Indian Institute of Technology Madras, Chennai 600036.

  10. Structural transformations of the synthetic salt 4`, 7-dihydroxyflavylium chloride in acid and basic aqueous solutions. Part 1-Ground state

    Energy Technology Data Exchange (ETDEWEB)

    Pina, F.; Benedito, L.; Melo, M.J.; Parola, A.J. [Centro de Quimica Fina e Biotecnologia. Departamento de Quimica FCT/UNL, Portugal (Portugal); Lima, J.C.; Macanita, A.L. [Instituto de Tecnologia Quimica e Biologica, Portugal (Portugal)

    1997-09-01

    A complete study of the structural pH dependent transformations of the synthetic flavylium salt 4`-7-dihydroxyflavylium chloride (DHF), occurring in aqueous solutions, including the basic region, is described. The kinetics study of the transformations occurring in acidic media (quinoidal base (A) {l_reversible} flavylium cation (AH{sup +}) {l_reversible} hemiacetal (B) {l_reversible} cis-chalcone (C-cis) {l_reversible} trans-chalcone (C-trans)) allowed to conclude that the cis-transisomerization is faster than the tautomerization and the hydration processes, which is unique in the anthocyanins family. Results obtained with the parent compound 4`-7-dimethoxyflavylium chloride (DMF)with relevance to this study are also presented. In equilibrated basic solutions the existence of acid-base equilibria involving the trans-Chalcone (C-trans) and its conjugated bases, (C-trans, and C``2-trans), was detected. Freshly prepared solutions at pH>7 show also the presence of a transient species identified as the ionized quinoidal base (A``-), which is almost completely converted into C``2-trans with a Ph dependent rate constant, (Author) 17 refs.

  11. Electrochemistry of actinide and lanthanide in molten salt system

    International Nuclear Information System (INIS)

    In the partition and transmutation processes of reprocessing of spent fuel or radioactive waste in nuclear power plant, the dry type reprocessing method using molten salt and liquid metal as a solvent is studied. Most especially researches on the electrolysis of the actinide nitride in the molten salts corresponding to reprocessing of nitride fuel cannot be found. This report is a research result about the electro-chemical behavior of actinide and lanthanide on the electrode in molten LiCL-KCL eutectic system. When anode potential was less than -0.4V in recovery of U metal by the molten salt electrolysis of UN, the electrolysis efficiency of the recovery is not influenced by the generation of UNCL and the oxidation-reduction reaction of U4+/U3+. Moreover, generation of a chlorination nitride was not seen in the case where PuN and NpN are used. (H. Katsuta)

  12. Fractionation of aqueous sodium salts by liquid-liquid extraction in aqueous two phase systems

    NARCIS (Netherlands)

    Milosevic, M.; Staal, K.J.J.; Bargeman, G.; Schuur, B.; Haan, de A.B.

    2014-01-01

    An important element in the work-up of brines is the separation of different ions present. Usually, energy consuming technologies, such as multi-stage evaporation, reverse osmosis, crystallization, and nanofiltration, are used to bring the composition of the brine to the required specification. Frac

  13. Reactivity control capability of fuel-salt processing system in a molten-salt breeder reactor

    International Nuclear Information System (INIS)

    An evaluation is made of the reactivity control capability of the fuel processing system (FPS) in a molten-salt breeder reactor. The principal functions required of the FPS are: (a) Isolation of 233Pa from regions of high neutron flux during its decay to 233U, and (b) the removal of fission products from the system. The FPS can very usefully serve also to control the primary system reactivity by appropriately utilizing its function of extracting uranium and reconstituting the fuel contained in the salt. The principles of operation are quite similar to the chemical shim control system currently installed in PWR's whereby the core reactivity, affected by changes in the moderator temperature, fuel burnup and transient Xe, is adjusted by regulating the concentration of boric acid introducted in the moderator as neutron absorber. The present study examines the capability of the FPS to follow transient Xe as in PWR's, and proves that the FPS should effectively serve as a system for adjusting not only long-term changes in reactivity but also short-term transient variations without any accompanying difficulties foreseen in operation. (auth.)

  14. 含盐体系汽液平衡数据的检验%VERIFICATION OF VAPOR-LIQUID EQUILIBRIUM DATA FOR SALT-CONTAINING SYSTEMS

    Institute of Scientific and Technical Information of China (English)

    孙仁义; 孙茜

    2002-01-01

    This paper regards the activity coefficient of salt in mixed solvents with constant composition as a function of vapor-liquid equilibrium data by means of ternary Gibbs-Duhem equation. A verification method including two independent criteria for vapor-liquid equilibrium data of salt-containing system is proposed on the bases of thermodynamics and the Debye-Hückel electrolytical solution theory.According to the criteria every experimental point can be verified by the calculation of its vapor-liquid equilibrium data.Not only is this method rigorous in the theory,but also very convenient in the application.Under the condition of fixing the ratio between two solvents it can be used for vapor-liquid equilibrium data verification of various salt-containing systems,whether the systems are isothemic or isobaric,aqueous or non-aqueous,up to saturated or non-saturated.

  15. Passivation behavior of Type 304 stainless steel in a non-aqueous alkyl carbonate solution containing LiPF{sub 6} salt

    Energy Technology Data Exchange (ETDEWEB)

    Myung, Seung-Taek [Department of Chemical Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate 020-8551 (Japan)], E-mail: smyung@iwate-u.ac.jp; Sasaki, Yusuke [Department of Chemical Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate 020-8551 (Japan); Saito, Takamitsu [Nissan Motors, 1 Natsushima, Yokosuka, Kanagawa 273-8523 (Japan); Sun, Yang-Kook [Department of Chemical Engineering, Hanyang University, Seungdong-Gu, Seoul 133-791 (Korea, Republic of); Yashiro, Hitoshi [Department of Chemical Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate 020-8551 (Japan)], E-mail: yashiro@iwate-u.ac.jp

    2009-10-01

    Passivation behavior of type 304 stainless steel in a non-aqueous alkyl carbonate solution containing LiPF{sub 6} salt was studied using electrochemical polarization, X-ray photoelectron spectroscopy (XPS) and time of flight-secondary ion mass spectroscopy (ToF-SIMS). Cathodic polarization to 0 V vs. Li/Li{sup +} resulted in most but not complete reduction of the air-formed film from oxides to metal on the stainless steel, as confirmed by XPS. For complete elimination of the air-formed film, the surface of the stainless steel was scratched under anodic polarization conditions. At 3 V vs. Li/Li{sup +} where an anodic current peak appeared, only an indistinct layer was recognized on the newly scratched surface, according to ToF-SIMS analysis. Above 4 V vs. Li/Li{sup +}, substantial passive films were formed, which were composed of oxides and fluorides of iron and chromium. The origin of oxide was due to water contained in the non-aqueous alkyl carbonate solution, and that of fluorides were the result of the decomposition of electrolytic salt, LiPF{sub 6}, especially at higher potential. The resultant passive films were stable in the non-aqueous alkyl carbonate solution containing LiPF{sub 6} salt.

  16. Monitoring system specifications: retrieval of surf from a salt repository

    International Nuclear Information System (INIS)

    The task of developing specifications for a reference monitoring system determined by repository environmental conditions, retrieval operations, and federal regulatory criteria is discussed. The monitoring system specified in this report is capable of measuring (1) package position and orientation, (2) vault deformation, (3) brine accumulation, (4) spent fuel dissolution, (5) temperature, (6) nuclear radiation, and (7) package condition with sufficient accuracy to provide data input to a general risk assessment model. In order to define a monitoring system which can provide probabilistic data on radiological risk to operating personnel and the general public for a salt mine repository, the following information is required: (1) a complete design of the salt SURF repository including inventory, density and waste package design details; (2) probalistic failure rate data on containment integrity of the SURF waste package; (3) probabilistic failure rate data on the monitoring system components

  17. Hydrodynamic simulation of a lithium chloride salt system

    International Nuclear Information System (INIS)

    A fused lithium chloride salt system's constitutive properties were evaluated and compared to a number of fluid properties, and water was shown to be an excellent simulant of lithium chloride salt. With a simple flow model, the principal scaling term was shown to be a function of the kinematic viscosity. A water mock-up of the molten salt was also shown to be within a ±3% error in the scaling analysis. This made it possible to consider developing water scaled tests of the molten salt system. Accurate flow velocity and pressure measurements were acquired by developing a directional velocity probe. The device was constructed and calibrated with a repeatable accuracy of ±15%. This was verified by a detailed evaluation of the probe. Extensive flow measurements of the engineering scale mockup were conducted, and the results were carefully compared to radial flow patterns of a straight blade stirrer. The flow measurements demonstrated an anti-symmetric nature of the stirring, and many additional effects were also identified. The basket design was shown to prevent fluid penetration into the fuel baskets when external stirring was the flow mechanism

  18. Molten Salt Test Loop (MSTL) system customer interface document.

    Energy Technology Data Exchange (ETDEWEB)

    Gill, David Dennis; Kolb, William J.; Briggs, Ronald D.

    2013-09-01

    The National Solar Thermal Test Facility at Sandia National Laboratories has a unique test capability called the Molten Salt Test Loop (MSTL) system. MSTL is a test capability that allows customers and researchers to test components in flowing, molten nitrate salt. The components tested can range from materials samples, to individual components such as flex hoses, ball joints, and valves, up to full solar collecting systems such as central receiver panels, parabolic troughs, or linear Fresnel systems. MSTL provides realistic conditions similar to a portion of a concentrating solar power facility. The facility currently uses 60/40 nitrate %E2%80%9Csolar salt%E2%80%9D and can circulate the salt at pressure up to 40 bar (600psi), temperature to 585%C2%B0C, and flow rate of 44-50kg/s(400-600GPM) depending on temperature. The purpose of this document is to provide a basis for customers to evaluate the applicability to their testing needs, and to provide an outline of expectations for conducting testing on MSTL. The document can serve as the basis for testing agreements including Work for Others (WFO) and Cooperative Research and Development Agreements (CRADA). While this document provides the basis for these agreements and describes some of the requirements for testing using MSTL and on the site at Sandia, the document is not sufficient by itself as a test agreement. The document, however, does provide customers with a uniform set of information to begin the test planning process.

  19. High-precision gigahertz-to-terahertz spectroscopy of aqueous salt solutions as a probe of the femtosecond-to-picosecond dynamics of liquid water

    CERN Document Server

    Vinh, N Q; Allen, S James; George, D K; Rahmani, A J; Plaxco, Kevin W

    2015-01-01

    Because it is sensitive to fluctuations occurring over femtoseconds to picoseconds, gigahertz-to-terahertz dielectric relaxation spectroscopy can provide a valuable window into water's most rapid intermolecular motions. In response, we have built a vector network analyzer dielectric spectrometer capable of measuring absorbance and index of refraction in this frequency regime with unprecedented precision. Using this to determine the complex dielectric response of water and aqueous salt solutions from 5.9 GHz to 1.12 THz (which we provide in the SI), we have obtained strong new constraints on theories of water's collective dynamics. For example, while the salt-dependencies we observe for water's two slower relaxations (8 and 1 ps) are easily reconciled with suggestions that they arise due to rotations of fully and partially hydrogen bonded molecules, respectively, the salt-dependence of the fastest relaxation (180 fs) appears difficult to reconcile with its prior assignment to liberations of single hydrogen bon...

  20. Ultrasonic-assisted synthesis of aqueous CdTe/CdS QDs in salt water bath heating

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Yinglian [College of Food Science and Engineering, Ocean University of China, Qingdao 266003, Shandong Province (China); College of Food Science and Engineering, Qingdao Agricultural University of China, Qingdao 266109, Shandong Province (China); Li, Chunsheng; Xu, Ying [College of Food Science and Engineering, Ocean University of China, Qingdao 266003, Shandong Province (China); Wang, Dongfeng, E-mail: wangdf@ouc.edu.cn [College of Food Science and Engineering, Ocean University of China, Qingdao 266003, Shandong Province (China)

    2014-09-01

    Highlights: • Ultrasonic promotes formation of crystal nucleus and QDs were synthesized in 0.5 h. • The new heating method provides a PLQY of up to 97.13%. • The synthesis mechanism of the core shell structure of the CdTe/CdS QDs was inferred. • The preparation method was efficient, simple and clean. - Abstract: A novel simple method for fast and efficient synthesis of aqueous CdTe/CdS quantum dots (QDs) with core–shell structure was developed by using salt water bath heating with the ultrasonic-assisted technique in this paper. The formation of crystal nucleus was promoted by ultrasonic and CdTe/CdS QDs with blue fluorescence were synthesized only in 0.5 h. The heat source was bath heating in salt water solution at 60% NaCl and the heating temperature could reach 105 °C. The heating method solved the biggest drawback of low photoluminescence quantum yield (PLQY) of ordinal bath heating in water. The preparation was cheap, simple and had less pollution to the environment. The properties of the CdTe/CdS QDs were thoroughly investigated by ultraviolet–visible (UV–vis), photoluminescence (PL), transmission electron microscope (TEM), laser size analysis, fourier transform infrared spectra (FTIR), X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDS). Different CdTe/CdS QDs with core shell structure were efficiently synthesized and the maximum PLQY could reach 97.13% when refluxing at 105 °C for 2 h. These QDs exhibited uniform dispersity, high fluorescence intensity, good optical property and long life of fluorescent. The synthesis mechanism of the core shell structure of the QDs was inferred that the Cd{sup 2+} might coordinate with sulfur (S) as well as thiol propionate (–SCH{sub 2}CH{sub 2}COO{sup −1}) to constitute two relatively thick compound layers on the QDs surface as passive shells.

  1. DESIGN OF ROBOTIC COLONIZER CONTROL SYSTEM FOR AQUEOUS ENVIRONMENT

    OpenAIRE

    C Venkatesh; C.CHANDRA SEKHAR

    2013-01-01

    Now a days there is a huge interest on underwater communication systems for various applications in order to explore aqueous environments. Intelligent robots and cooperative multi- agent robotic systems can be very efficient tools to speed up search and research operations in remote areas. Robots are also useful to do jobs inareas and in situations that are hazardous for human, they can go anywhere that is not reachable my humans and can go into gaps and move trough small holes that are impos...

  2. Advanced Aqueous Separation Systems for Actinide Partitioning

    Energy Technology Data Exchange (ETDEWEB)

    Nash, Kenneth L.; Clark, Sue; Meier, G Patrick; Alexandratos, Spiro; Paine, Robert; Hancock, Robert; Ensor, Dale

    2012-03-21

    One of the most challenging aspects of advanced processing of spent nuclear fuel is the need to isolate transuranium elements from fission product lanthanides. This project expanded the scope of earlier investigations of americium (Am) partitioning from the lanthanides with the synthesis of new separations materials and a centralized focus on radiochemical characterization of the separation systems that could be developed based on these new materials. The primary objective of this program was to explore alternative materials for actinide separations and to link the design of new reagents for actinide separations to characterizations based on actinide chemistry. In the predominant trivalent oxidation state, the chemistry of lanthanides overlaps substantially with that of the trivalent actinides and their mutual separation is quite challenging.

  3. Phase diagrams and water activities of aqueous ammonium salts of malonic acid.

    Science.gov (United States)

    Beyer, Keith D; Richardson, Michael; Reusch, Breanna

    2011-04-14

    Malonic acid has been observed in the free troposphere and as a component of tropospheric aerosol, among other dicarboxylic acids. These aerosols can uptake ammonia, which partially or completely neutralizes the acids. Therefore, the impact of ammoniated dicarboxylic acids on the phases that can exist in aerosols at atmospheric temperatures needs investigation. To that end, the low temperature, solid/liquid phase diagrams of ammonium hydrogen malonate/water, ammonium malonate/water, and triammonium hydrogen malonate/water have been investigated with differential scanning calorimetry and infrared spectroscopy of thin films. Results show that the order of increasing solubility is triammonium hydrogen malonate, ammonium hydrogen malonate, malonic acid, and ammonium malonate. We have also determined a hydrate may form in the ammonium malonate system and decompose below 240 K. We report water activities at the ice melting points for each system up to the respective eutectic concentrations, and find for a given mole fraction of water, increasing ammonium content leads to decreasing water activity coefficients. PMID:21428389

  4. Partition behavior of surfactants, butanol, and salt during application of density-modified displacement of dense non-aqueous phase liquids

    International Nuclear Information System (INIS)

    Highlights: ► Aqueous surfactant increases the partition of butanol aqueous phase. ► Water partition to NAPL phase via butanol and surfactant in NAPL phase. ► PCE partition to aqueous phase by solubilization into micelles. ► Surfactants cause the dramatically partition of water to NAPL phase. ► Aqueous salt dispels surfactant to NAPL phase. -- Abstract: Density-modified displacement (DMD) is a recent approach for removal of trapped dense NAPL (DNAPL). In this study, butanol and surfactant are contacted with the DNAPL to both reduce the density as well as release the trapped DNAPL (perchloroethylene: PCE). The objective of the study was to determine the distribution of each component (e.g., butanol, surfactant, water, PCE) between the original aqueous and PCE phases during the application of DMD. The results indicated that the presence of the surfactant increased the amount of n-butanol required to make the NAPL phase reach its desired density. In addition, water and anionic surfactant were found to partition along with the BuOH into the PCE phase. The water also found partitioned to reverse micelles in the modified phase. Addition of salt was seen to increase partitioning of surfactant to BuOH containing PCE phase. Subsequently, a large amount of water was solubilized into reverse micelles which lead to significantly increase in volume of the PCE phase. This work thus demonstrates the role of each component and the implications for the operation design of an aquifer treatment using the DMD technique

  5. Salt-effects in aqueous surface-active ionic liquid 1-dodecyl-3-methylimidazolium bromide solutions: Volumetric and compressibility property changes and critical aggregation concentration shifts

    International Nuclear Information System (INIS)

    Graphical abstract: Plot of ϕV against mIL, for solutions of [C12mim]Br in water (solid lines) and in aqueous solutions of 0.035 mol · kg−1 NaCl (dotted lines) at: ○ and ●, T = 288.15 K; △ and ▴,T = 293.15 K; □ and ■, T = 298.15 K. - Highlights: • Salt effect on the aggregation of [C12mim]Br in aqueous solutions were studied. • The effect of 6 chloride electrolytes and 5 sodium electrolytes were investigated. • Investigated electrolytes have salting-out effect on the aggregation of [C12mim]Br. • Changes in the volumes and compressibilities upon micellization were derived. - Abstract: Systematic studies on the volumetric and compressibility properties of aqueous solutions of model surface-active ionic liquid 1-dodecyl-3-methylimidazolium bromide ([C12mim]Br) are performed in the absence and presence of a large series of electrolytes in order to achieve a deeper understanding about the molecular mechanism behind the specific salt effect on the aggregation behavior of [C12mim]Br in aqueous solution. For this purpose, 6 chloride electrolytes (NaCl, KCl, NH4Cl, (CH3)4NCl, MgCl2 and FeCl3) and 5 sodium electrolytes (NaCl, NaNO3, Na2CO3, Na2SO4, and Na3Cit.) were used in order to individualize the effect of the anion and the cation. The values of the critical aggregation concentration (CAC) were obtained and it was found that all the investigated electrolytes have salting-out effect on the aggregation of [C12mim]Br in aqueous solutions, leading to significant downward shifts of the CAC. The magnitude of the shifts depends on the water-structuring nature of the electrolyte and follows the Hofmeister series. Changes in the apparent molar volumes and isentropic compressibilities upon micellization were derived using a pseudophase-transition approach and the infinite dilution apparent molar properties of the monomer and micellar form of [C12mim]Br were determined

  6. Partition of lead in a milk-pectin aqueous biphasic system with complexing agents

    International Nuclear Information System (INIS)

    Aqueous two-phase systems allow partition of metal ions in nondenaturing conditions. From the fresh skim bovine milk spiked with 212Pb and agitated with 4% water solution of apple pectin (degree of esterification - 70%), less than 2.3% is recovered to the pectin phase and in the case of pasteurized milk less than 3.0%. Complexation with chelate forming agents was studied. Aminoacids as glycine, alanine and histidine do not exert influence on the yield, but the recovery in the pectin phase was 22% for cysteine, and 80% in the case of EdtacalTM (calcium salt of ethylenediaminetetraacetic acid). The retention of lead in milk phase is extraordinarily high as compared to strontium and corresponds to the behavior of trivalent ions. (author)

  7. Poly(ionic liquid)s as phase splitting promoters in aqueous biphasic systems.

    Science.gov (United States)

    João, Karen G; Tomé, Liliana C; Isik, Mehmet; Mecerreyes, David; Marrucho, Isabel M

    2015-11-01

    Aqueous biphasic systems (ABSs) provide a sustainable and efficient alternative to conventional liquid-liquid extraction techniques with volatile organic solvents, and can be used for the extraction, recovery, and purification of diverse solutes. In this work, and for the first time, ABSs composed of poly(ionic liquid)s (PILs) and inorganic salts were measured at 25 °C and atmospheric pressure. New PILs having pyrrolidinium polycations combined with different counter-anions, namely acetate [Ac](-), trifluoroacetate [TFAc](-), hexanoate [Hex](-), adipate [Adi](-), and citrate [Cit](-) were synthesized, by a simple and environmentally-friendly procedure, and characterized. The effect of the PIL features, namely molecular weight and anionic character, and other experimental variables, such as temperature, on the phase splitting ability was researched. The aptitude of the studied ABS to be implemented as separation technologies was also evaluated through the use of a model biomolecule, tryptophan. PMID:26421939

  8. Protein partitioning in poly(ethylene glycol)/sodium polyacrylate aqueous two-phase systems.

    Science.gov (United States)

    Johansson, Hans-Olof; Magaldi, Flavio Musa; Feitosa, Eloi; Pessoa, Adalberto

    2008-01-18

    The partition of hemoglobin, lysozyme and glucose-6-phosphate dehydrogenase (G6PDH) in a novel inexpensive aqueous two-phase system (ATPS) composed by poly(ethylene glycol) (PEG) and sodium polyacrylate (NaPA) has been studied. The effect of NaCl and Na(2)SO(4), pH and PEG molecular size on the partitioning has been studied. At high pH (above 9), hemoglobin partitions strongly to the PEG-phase. Although some precipitation of hemoglobin occurs, high recovery values are obtained particularly for lysozyme and G6PDH. The partitioning forces are dominated by the hydrophobic and electrochemical (salt) effects, since the positively charged lysozyme and negatively charged G6PDH partitions to the non-charged PEG and the strongly negatively charged polyacrylate enriched phase, respectively. PMID:18078945

  9. High-Level Waste Salt Disposition Systems Engineering Team Final Report, Volumes I, II, and III

    International Nuclear Information System (INIS)

    This report describes the process used and results obtained by the High Level Waste Salt Disposition Systems Engineering Team to select a primary and backup alternative salt disposition method for the Savannah River Site

  10. The molten salt reactors (MSR) pyro chemistry and fuel cycle for innovative nuclear systems

    International Nuclear Information System (INIS)

    precipitation processes); cold salt: potentiality and preliminary results; TOPIC: redox control of MSR fuel (MSR: nominal operating conditions for the reprocessing process and redox control); technical aspects of R and D of some advanced non-aqueous reprocessing technologies for MSR systems (promising innovative separation and partitioning processes for the MSR fuel cycle); nominal operating conditions for MSR reprocessing process - data base needed and experiments for reprocessing validation; corrosion and materials for MSR and for pyro-chemistry processes; MSR reactor physics - dynamic behaviour; what safety principles for MSR? (MSR and integrated cycle (IFR) safety approach); experimental programmes in the frame of the SPHINX project of MS transmuter (programme of irradiated probes BLANKA, experimental facilities (MSR)); ISTC 1606 status - experimental study of molten salt technology for safe, low-waste and proliferation resistant treatment of radioactive waste and plutonium in accelerator-driven and critical systems. (J.S.)

  11. Synthesis and Self-Assembly of Triangulenium Salts

    DEFF Research Database (Denmark)

    Shi, Dong

    -processed self-assembling method was developed to make aggregates with uniform morphologies and excellent stabilities in an equilibrium state either with pure ATOTA+ salts or with mixed systems of ATOTA+ salts and lipid molecules in aqueous media. Special emphasis was given to effects of the counterions in......-assembly and triangulenium salts. Chapters 3 to 6 are mainly focused on the synthesis and self-assembly of trioxatriangulenium salts in aqueous media. In particular, chapter 3 reports a direct selfassembly of a synthetic triangulenium salt mixed with DMPC lipid (5/95 by molar ratio) to make mono disperse......This thesis describes the design and synthesis of asymmetrically substituted amphiphilic tis(dialkylamino)trioxiatriangulenium (ATOTA+) salts with different counter ions. Attention was focused on exploring the assembling properties of the ATOTA+ salts in aqueous media. A direct vortexing...

  12. Stoichiometric C6-oxidation of hyaluronic acid by oxoammonium salt TEMPO⁺Cl⁻ in an aqueous alkaline medium.

    Science.gov (United States)

    Ponedel'kina, Irina Yu; Khaibrakhmanova, Elvira A; Tyumkina, Tatyana V; Romadova, Irina V; Odinokov, Victor N

    2015-10-01

    This paper reports the selective oxidation of hyaluronic acid (HA) by stoichiometric quantity of 2,2,6,6-tetramethylpiperidine-1-oxoammonium chloride (TEMPO(+)) in aqueous alkaline medium. High efficiency of the HA oxidation and quantitative yield of carboxy-HA per starting TEMPO(+), as well as unusual behavior of the oxidation system generating an oxygen upon alkali-induced oxoammonium chloride decomposition are demonstrated. The scheme for HA oxidation involving both TEMPO(+) and oxygen produced upon the TEMPO(+)Cl(-) decomposition and/or air oxygen is proposed. For comparison, the data on stoichiometric oxidation of such substrates as dermatan sulfate, water-soluble potato starch, methyl 2-acetamido-2-deoxy-β-d-glucopyranoside and ethanol are presented. PMID:26076602

  13. Effect of temperature on the (liquid + liquid) equilibrium for aqueous solution of nonionic surfactant and salt: Experimental and modeling

    Energy Technology Data Exchange (ETDEWEB)

    Foroutan, Masumeh [Physical Chemistry Department, School of Chemistry, College of Science, University of Tehran, 14155-6455 Enghelab Avenue, Tehran (Iran, Islamic Republic of)], E-mail: foroutan@khayam.ut.ac.ir; Heidari, Nosrat; Mohammadlou, Maryam [Chemistry Department, Faculty of Science, Uremia University, Uremia (Iran, Islamic Republic of); Sojahrood, Amin Jafari [Physics Department, Faculty of Science, Uremia University, Uremia (Iran, Islamic Republic of)

    2008-07-15

    The effect of temperature on the (liquid + liquid) equilibrium of the aqueous solution of surfactant polyoxyethylene cetylether (with abbreviation name Brij 58) and diammonium hydrogen phosphate has been investigated at T = (303.15, 313.15, 323.15, and 333.15) K. The Flory-Huggins equation with two electrostatic terms (Debye-Huckle and Pitzer-Debye-Huckle equations) was used to correlate the phase behavior of this system. Good agreement has been found between experimental and calculated data from both models. The results indicated that the enlargement of the two-phase region upon increasing the temperature. Additionally temperature dependency of the parameters of the Flory-Huggins model has been calculated.

  14. Effect of temperature on the (liquid + liquid) equilibrium for aqueous solution of nonionic surfactant and salt: Experimental and modeling

    International Nuclear Information System (INIS)

    The effect of temperature on the (liquid + liquid) equilibrium of the aqueous solution of surfactant polyoxyethylene cetylether (with abbreviation name Brij 58) and diammonium hydrogen phosphate has been investigated at T = (303.15, 313.15, 323.15, and 333.15) K. The Flory-Huggins equation with two electrostatic terms (Debye-Huckle and Pitzer-Debye-Huckle equations) was used to correlate the phase behavior of this system. Good agreement has been found between experimental and calculated data from both models. The results indicated that the enlargement of the two-phase region upon increasing the temperature. Additionally temperature dependency of the parameters of the Flory-Huggins model has been calculated

  15. Molten salt thermal energy storage systems. Project 8981, final report

    Energy Technology Data Exchange (ETDEWEB)

    Maru, H.C.; Dullea, J.F.; Kardas, A.; Paul, L.

    1978-03-01

    The feasibility of storing thermal energy at temperatures of 450/sup 0/ to 535/sup 0/C (850/sup 0/ to 1000/sup 0/F) in the form of latent heat of fusion has been examined for over 30 inorganic salts and salt mixtures. Alkali carbonate mixtures are attractive as phase-change storage materials in this temperature range because of their relatively high storage capacity and thermal conductivity, moderate cost, low volumetric expansion upon melting, low corrosivity, and good chemical stability. An equimolar mixture of Li/sub 2/CO/sub 3/ and K/sub 2/CO/sub 3/, which melts at 505/sup 0/C with a latent heat of 148 Btu/lb, was chosen for experimental study. The cyclic charge/discharge behavior of laboratory- and engineering-scale systems was determined and compared with predictions based on a mathematical heat-transfer model that was developed during this program. The thermal performance of one engineering-scale unit remained very stable during 1400 hours of cyclic operation. Several means of improving heat conduction through the solid salt were explored. Areas requiring further investigation have been identified.

  16. Systems engineering management plan for the Salt Repository Project

    International Nuclear Information System (INIS)

    This document presents the plan for using systems engineering in conducting and managing the technical work of the Salt Repository Project (SRP) of the US Department of Energy's Civilian Radioactive Waste Management Program. The need for preparing a Systems Engineering Management Plan (SEMP) is traced back to relevant DOE directives. These directives are interpreted as SRP requirements in the context of the Mined Geologic Disposal System. The strategy for conducting systems engineering on the SRP, including the role of the systems engineering process, is then described. The SEMP also designates who in the project organization will be responsible for carrying out the activities. Finally, the management tools that are used to implement the systems engineering process, including associated documentation on the SRP, are described

  17. The determination of thermodynamic characteristics of extraction equilibria in the systems containing ammonium salts and organic phosphorus compounds

    International Nuclear Information System (INIS)

    Consideration is being given to empirical methods of calculation and mathematical models, enabling to describe rather simple and precisely a thermodynamic equilibrium in extractive systems based on alkylammonium salts and organicophosphorus compounds. It is shown that Pitzer's and Mikulin's methods are the most suitable ones for calculation of thermodynamic activity of components in aqueous phase. The organic phase can be described most precisely by the ideal associative solution model, which takes into account the difference of association constants and additional solvation of metal-containing complex by extractant molecules. Equations for calculating association constants of tributylphosphate (TBP) and alkylammonium salts in organic solvents are given; values of additional solvation constants are presented for the following systems: M(NO3)n-TBP-benzene (where M=Ce3+, Pr3+, UO22+, Th4+; n=2, 3, 4) and Ce(Eu)(NO3)3-TLA·HNO3-CCl4, where TLA·HNO3 - trilaurylammonium nitrate

  18. Separation of Nanoparticles in Aqueous Multiphase Systems through Centrifugation

    KAUST Repository

    Akbulut, Ozge

    2012-08-08

    This paper demonstrates the use of aqueous multiphase systems (MuPSs) as media for rate-zonal centrifugation to separate nanoparticles of different shapes and sizes. The properties of MuPSs do not change with time or during centrifugation; this stability facilitates sample collection after separation. A three-phase system demonstrates the separation of the reaction products (nanorods, nanospheres, and large particles) of a synthesis of gold nanorods, and enriches the nanorods from 48 to 99% in less than ten minutes using a benchtop centrifuge. © 2012 American Chemical Society.

  19. Correlation between the Increasing Conductivity of Aqueous Solutions of Cation Chlorides with Time and the “Salting-Out” Properties of the Cations

    Directory of Open Access Journals (Sweden)

    Nada Verdel

    2016-02-01

    Full Text Available The time-dependent role of cations was investigated by ageing four different aqueous solutions of cation chlorides. A linear correlation was found between the cations’ Setchenov coefficient for the salting-out of benzene and the increase in the conductivity with time. The conductivity of the structure-breaking cations or the chaotropes increased more significantly with time than the conductivity of the kosmotropes. Since larger water clusters accelerate the proton or hydroxyl hopping mechanism, we propose that the structuring of the hydration shells of the chaotropes might be spontaneously enhanced over time.

  20. Partitioning of glycomacropeptide in aqueous two-phase systems

    OpenAIRE

    Silva, C. A. S.; Coimbra, Jane Sélia dos Reis; Rojas, Edwin Elard Garcia; Teixeira, J. A.

    2009-01-01

    The partition behavior of glycomacropeptide (GMP) was determined in polyethylene glycol (PEG) and sodium citrate aqueous two-phase systems (ATPS). It was found that the partitioning of GMP depends on PEG molar mass, tie line length, pH, NaCl concentration and temperature. The obtained data indicates that GMP is preferentially partitioned into the PEG phase without addition of NaCl at pH 8.0. Larger tie line lengths and higher temperatures favor GMP partition to the PEG phase. Furt...

  1. IS MONO SODIUM GLUTAMATE SALT (MSG HARMFUL TO LIVING SYSTEMS?

    Directory of Open Access Journals (Sweden)

    Batul Shabbir*, Zehra Fatima, VVenugopal Rao and Shoba Ganesh

    2014-08-01

    Full Text Available Monosodium glutamate (MSG, also known as sodium glutamate, is the sodium salt of glutamic acid, one of the most abundant naturally occurring non-essential amino acids. A widespread and silent killer that’s worse for your health than alcohol, nicotine and many drugs is likely lurking in your kitchen cabinets right now. “It” is monosodium glutamate (MSG, a flavor enhancer that’s known widely as an addition to Chinese food, but that’s actually added to thousands of the foods you and your family regularly eat, especially if you are like most  of the people who eat the majority of your food as processed foods or in restaurants. MSG is one of the worst food additives on the market and is used in canned soups, crackers, meats, salad dressings, frozen dinners and much more. It’s found in your local supermarket and restaurants, in your child’s school cafeteria and, amazingly, even in baby food and infant formula. We tested the efficacy of toxicity of MSG on certain living cells (epithelial cells of buccal cavity, blood cells, onion root tips and DNA extracted from onions. We found that at low concentrations the salt does no harm whatsoever but as concentration is increased (10% and above harmful effects like disintegrating nuclei and malformed cells were observed. Therefore we conclude that though it has no effects at low concentration, it may harm the living system if consumed without any inhibition at high concentrations (daily eating of fast foods and processed foods or via accumulation of salt in the system resulting in high concentration over a period of time.

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

    Science.gov (United States)

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

    2016-02-01

    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.

  3. Thorium fuel cycle technology for molten salt reactor systems

    International Nuclear Information System (INIS)

    Molten Salt Reactor (MSR) is classified as the non-classical nuclear type based on the specific featured coming out from the use of liquid fuel circulating in the MSR primary circuit. Other uniqueness of the reactor type is based on the fact that the primary or fuel circuit of the reactor in operation for a long run. MSR is the only reactor system, which can be operated with thorium fuel within the pure 232Th - 233U fuel cycle with the breeding factor significantly higher than one. It can bring several advantages, mainly in the radioactive waste management, thanks to minimized production higher actinides. With respects to all these facts and features, the fuel cycle aspects of MSR system are quite complicated, especially if the technology shall guarantee all possible advantages of MSR system concurrently with good economy, technological safety and reliability and inevitable proliferation resistance

  4. Specific Na+ and K+ Cation Effects on the Interfacial Water Molecules at the Air/Aqueous Salt Solution Interfaces Probed with Non-resonant Second Harmonic Generation (SHG)

    CERN Document Server

    Bian, Hong-tao; Guo, Yuan; Wang, Hong-fei

    2008-01-01

    Here we report the polarization dependent non-resonant second harmonic generation (SHG) measurement of the interfacial water molecules at the aqueous solution of the following salts: NaF, NaCl, NaBr, KF, KCl, and KBr. Through quantitative polarization analysis of the SHG data,the orientational parameter D value and the relative surface density of the interfacial water molecules at these aqueous solution surfaces were determined. From these results we found that addition of each of the six salts caused increase of the thickness of the interfacial water layer at the surfaces to a certain extent. Noticeably, both the cations and the anions contributed to the changes, and the abilities to increase the thickness of the interfacial water layer were in the following order: KBr > NaBr > KCl > NaCl ~ NaF > KF. Since these changes can not be factorized into individual anion and cation contributions, there are possible ion pairing or association effects, especially for the NaF case. We also found that the orientational ...

  5. DOE workshop: Sedimentary systems, aqueous and organic geochemistry

    Energy Technology Data Exchange (ETDEWEB)

    1993-07-01

    A DOE workshop on sedimentary systems, aqueous and organic geochemistry was held July 15-16, 1993 at Lawrence Berkeley Laboratory. Papers were organized into several sections: Fundamental Properties, containing papers on the thermodynamics of brines, minerals and aqueous electrolyte solutions; Geochemical Transport, covering 3-D imaging of drill core samples, hydrothermal geochemistry, chemical interactions in hydrocarbon reservoirs, fluid flow model application, among others; Rock-Water Interactions, with presentations on stable isotope systematics of fluid/rock interaction, fluid flow and petotectonic evolution, grain boundary transport, sulfur incorporation, tracers in geologic reservoirs, geothermal controls on oil-reservoir evolution, and mineral hydrolysis kinetics; Organic Geochemistry covered new methods for constraining time of hydrocarbon migration, kinetic models of petroleum formation, mudstones in burial diagenesis, compound-specific carbon isotope analysis of petroleums, stability of natural gas, sulfur in sedimentary organic matter, organic geochemistry of deep ocean sediments, direct speciation of metal by optical spectroscopies; and lastly, Sedimentary Systems, covering sequence stratigraphy, seismic reflectors and diagenetic changes in carbonates, geochemistry and origin of regional dolomites, and evidence of large comet or asteroid impacts at extinction boundaries.

  6. Photolysis of difloxacin and sarafloxacin in aqueous systems.

    Science.gov (United States)

    Prabhakaran, Deivasigamani; Sukul, Premasis; Lamshöft, Marc; Maheswari, Mohan Akhila; Zühlke, Sebastian; Spiteller, Michael

    2009-10-01

    The photodegradation of two fluoroquinolone veterinary antibiotics, difloxacin (DIF) and sarafloxacin (SARA) has been explored for the first time in aqueous systems. The study was performed to evaluate the influence of pH, inorganics, humic substances, and other additives. The drugs followed first-order degradation kinetics in matrix free aqueous medium with a rate constant 'k' value of 0.82 and 0.26 h(-1) for DIF and SARA, respectively. Studies performed at various pH revealed that the photolysis rates dropped sharply at pH >7 for DIF, while SARA dissipated faster with increasing pH. Humic substances acted as light barriers by attenuating the light intensity, to retard the drug degradation process. However, rapid drug dissipation was observed in the presence of additives like acetone, hydrogen peroxide, and phosphates, while inorganics such as fluoride, nitrate, and sulfate did not influence the drug photodegradation. Studies on the photolysis of DIF and SARA in river water revealed that both the drugs degraded rapidly under conditions that were relevant to natural systems, following direct photolysis mechanism. It was observed that SARA was the primary photoproduct of DIF and showed relatively a higher persistence than DIF. The findings were also substantiated by the quantum yield (Phi(c)) calculations. The analytical measurements were carried out with LC-MS/MS. PMID:19751946

  7. DOE workshop: Sedimentary systems, aqueous and organic geochemistry

    International Nuclear Information System (INIS)

    A DOE workshop on sedimentary systems, aqueous and organic geochemistry was held July 15-16, 1993 at Lawrence Berkeley Laboratory. Papers were organized into several sections: Fundamental Properties, containing papers on the thermodynamics of brines, minerals and aqueous electrolyte solutions; Geochemical Transport, covering 3-D imaging of drill core samples, hydrothermal geochemistry, chemical interactions in hydrocarbon reservoirs, fluid flow model application, among others; Rock-Water Interactions, with presentations on stable isotope systematics of fluid/rock interaction, fluid flow and petotectonic evolution, grain boundary transport, sulfur incorporation, tracers in geologic reservoirs, geothermal controls on oil-reservoir evolution, and mineral hydrolysis kinetics; Organic Geochemistry covered new methods for constraining time of hydrocarbon migration, kinetic models of petroleum formation, mudstones in burial diagenesis, compound-specific carbon isotope analysis of petroleums, stability of natural gas, sulfur in sedimentary organic matter, organic geochemistry of deep ocean sediments, direct speciation of metal by optical spectroscopies; and lastly, Sedimentary Systems, covering sequence stratigraphy, seismic reflectors and diagenetic changes in carbonates, geochemistry and origin of regional dolomites, and evidence of large comet or asteroid impacts at extinction boundaries

  8. Ultrasonic relaxation study of preferential solvation in quasi-two-components aqueous solutions of amides and zinc salts.

    Science.gov (United States)

    Miecznik, P; Golebiewski, Z

    2004-04-01

    To investigate the effect of preferential solvation the ultrasonic attenuation (2-50 MHz) and velocities (3 MHz) of ZnCl(2) and 2-chloroacetamide (ClCH(2)CONH(2)) in water and its quasi-binary mixtures with the ratio (ZnCl(2)+ClCH(2)CONH(2)):H(2)O=1:55 at 298.15 K have been measured. The creation of specific complexes in the ClCH(2)CONH(2)-H(2)O-ZnCl(2) system have a relaxational character which, within the measurements of ultrasonic absorption in the frequency range 2-50 MHz, have been observed. On the base of these properties the kinetic and dynamic parameters of the observed relaxation have been calculated. To bring into relief the influence of Cl atom in the 2-chloroacetamide molecules for complexation process it has been investigated also the system AA-H(2)O-ZnCl(2). The next step of searching was to investigate the system of CHAA-H(2)O-ZnBr(2), to reduce the influence of Cl atom within ZnCl(2) molecule at the complexation process. The main aim of presented study was to investigate the possibility of complexation in the aqueous solutions of ZnCl(2) with the part of 2-ClCH(2)CONH(2) (CHAA). With regard of big complexing ability of zinc, there exist a theoretical possibility of attachment CHAA to the inner coordination sphere of zinc through chloride atom. There can create here outer-sphere as well as inner-sphere complexes. As a results the observed relaxation processes have been attributed to creation and disintegration the following complexes: Zn(H(2)O)(2)(CHAA)(4)(2+) and Zn(2+)(H(2)O)(3)(CHAA)Cl(2)(-). PMID:15047358

  9. Heats of Mixing in Binary Systems of Molten Salts

    International Nuclear Information System (INIS)

    The heat of mixing is an important thermodynamic property in binary mixtures. As a result of the recent development of high-temperature calorimetry we have been able to determine directly the heat of mixing in binary systems of molten salts. In this work we present the results of thermochemical measurements carried out in our laboratories for the systems (Rb-K)Cl; (Rb-Na)Cl; (Ag-Na)Cl; (Na-K)Br and(Br-Cl)Na for different concentrations and temperatures. In our view, the most significant components of the heat of mixing are the ionic contribution and the polarization energy of the ions. Consequently, use could be made of a relation of the form: ΔHM = Qi - Qp. The heat of mixing can then have either positive or negative values depending on the sign and the preponderance of the Qi and Qp energies. (author)

  10. Thermal decomposition kinetic of salt hydrates for heat storage systems

    International Nuclear Information System (INIS)

    Highlights: • Charging of closed thermochemical energy storage concept was studied numerically. • Pressure effect in kinetic modelling for thermochemical energy storage is presented. • A partial differential equations system was developed and applied. • Prediction of charging process in a thermochemical heat storage process is provided. - Abstract: Thermal energy or heat storage systems using chemical reactions to store and release energy operate in charging and discharging phases. The charging phase in this work is a dehydration process with constant heating rate decomposing salt hydrates as chemical components resulting in the obtention of a less hydrated or anhydrous form and, at the same time, storing the released heat (energy storage). Latest research on thermal decomposition of several salt-hydrates concerned experimental and numerical investigations (Huang et al., 2010; Sugimoto et al., 2007). A mathematical model of heat and mass transfer in a fixed-bed reactor for heat storage is proposed on the basis of a set of partial differential equations (PDEs) controlling the balances of mass, conversion, and energy in the bed and the reactor. These PDEs are numerically solved by means of the finite element method using Comsol Multiphysics 4.3a. The objective of this paper is to describe an adaptive modelling approach and establish a correct set of PDEs describing the physical system and appropriate parameters for simulating the thermal decomposition process. Thus it could help in the design of thermal energy storage system. The recommendations the International Confederation for Thermal Analysis and Calorimetry (Vyazovkin et al., 2011) on kinetic behaviour were used to explain transport phenomena and reactions mechanism in gas and solid phases. The generalized Prout–Tompkins equation was therefore adopted with some modifications based on thermal analysis experiments and literature. The experimental data from the TGA–DSC measurements are then used to

  11. Development of High-Temperature Transport System for Molten Salt in Pyroprocessing

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Sung Ho; Kim, In Tae; Park, Sung Bin [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2014-05-15

    The electrorefining process, which is a key process in pyroprocessing, is composed of two parts, electrorefining to deposit a uranium with a solid cathode and electrowinning to co-deposit TRU and RE with a liquid cadmium cathode (LCC). As the electrorefining operation proceedes, TRU and RE are accumulated in electrolyte LiCl-KCl salt, and after the electrorefining process, the molten salt used in an electrorefining reactor should by transported to the next process, the electrowinning process, to recover U/TRU/RE; Thus, a molten salt transfer system by suction is now being developed. An apparatus for suction transport experiments was designed and constructed for the development of high- temperature molten salt transport technology. Suction transport experiments were performed using LiC-KCl eutectic salt. The feasibility of pyro-reprocessing has been demonstrated through many laboratory-scale experiments. In pyroprocessing, a eutectic LiCl-KCl salt was used as a liquid elextrolyte for a recovery of actinides. However, reliable transport technologies for these high temperature liquids have not yet been developed. A preliminary study on high-temperature transport technology for molten salt by suction is now being carried out. In this study, three different salt transport technologies (gravity, suction pump, and centrifugal pump) were investigated to select the most suitable method for molten salt transport. An apparatus for suction transport experiments was designed and installed for the development of high-temperature molten salt transport technology. Basic preliminary suction transport experiments were carried out using the prepared LiC-KCl eutectic salt at 500 .deg. C to observe the transport behavior of LiCl-KCl molten salt. In addition, a PRIDE salt transport system was designed and installed for an engineering-scale salt transport demonstration. Several types of suction transport experiments using molten salt (LiCl-KCl eutectics) for the development of a high

  12. SANS study of micelle formation in aqueous mixed solutions of sodium and magnesium dodecylsulfates with added salts

    International Nuclear Information System (INIS)

    Complete text of publication follows. Mixtures of two anionic surfactants -sodium and magnesium didecyl sulphates- in heavy water were studied by small-angle neutron scattering (SANS) at various relative and total concentrations of the surfactants and various salt contents (NaCl and MgCl2). The average aggregation number and the effective fractional charge of mixed micelles were determined by fitting the data with the spherical or ellipsoidal shape model for the form factor and with the rescaled mean spherical approximation (RMSA) model for the structural factor. There are differences in the dependence of the characteristics of the mixed micelles formation on the relative concentration of the surfactants for the cases of their small and high total concentration. The changes in the micelle structure under salt addition are affected by the king of the salt. (author)

  13. Physicochemical characterization of novel aqueous two-phase system: gemini surfactant 12-2-12/NaBr/H2O.

    Science.gov (United States)

    Yue, Ling; He, Zimeng; Zhu, Yunfeng; Shang, Yazhuo; Liu, Honglai

    2015-04-01

    A novel aqueous two-phase system (ATPS) only containing Gemini surfactant ethanediyl-1,2-bis(dodecyldimethylammonium bromide) and an inorganic salt sodium bromide was designed, and the physicochemical properties of the ATPS were investigated systematically. The results have shown that the coexisting two phases, one surfactant-rich and the other salt-rich, are stable and the phase behavior, volume ratio, and extraction efficiency of ATPS are strongly influenced by contents of surfactant and salt. The novel ATPS here investigated have potential application in partitioning and analysis of biomaterials. Compared with other complicated surfactant-based ATPS, the surfactant concentration for the formation of ATPS is much lower, which implies that the studied system is potentially more economical for purification and separation of biomaterials. Meanwhile, the surfactant can be recycled by altering salt concentration in ATPS. Lyotropic liquid crystal was found in the bottom phase besides micelles under different conditions. The salting-out effect may be the driving force of ATPS formation for the studied "living polymer"/salt system. However, the coexistence of micelles with different microstructures is the necessary condition of phase separation. The current studies not only present a new ATPS for partitioning and analysis of biomaterials but also have a great significance on rational use of Gemini surfactants. PMID:25649445

  14. Advanced Thermal Storage System with Novel Molten Salt: December 8, 2011 - April 30, 2013

    Energy Technology Data Exchange (ETDEWEB)

    Jonemann, M.

    2013-05-01

    Final technical progress report of Halotechnics Subcontract No. NEU-2-11979-01. Halotechnics has demonstrated an advanced thermal energy storage system with a novel molten salt operating at 700 degrees C. The molten salt and storage system will enable the use of advanced power cycles such as supercritical steam and supercritical carbon dioxide in next generation CSP plants. The salt consists of low cost, earth abundant materials.

  15. Radiation-Engineered Functional Nanoparticles in Aqueous Systems.

    Science.gov (United States)

    Dispenza, Clelia; Grimaldi, Natascia; Sabatino, Maria Antonietta; Soroka, Inna L; Jonsson, Mats

    2015-05-01

    Controlled synthesis of nanoscalar and nanostructured materials enables the development of novel functional materials with fine-tuned optical, mechanical, electronic, magnetic, conductive and catalytic properties that are of use in numerous applications. These materials have also found their potential use in medicine as vehicles for drug delivery, in diagnostics or in combinations thereof. In principle, nanoparticles can be divided into two broad categories, organic and inorganic nanoparticles. For both types of nanoparticles there are numerous possible synthetic routes. Considering the large difference in nature of these materials and the elementary reactions involved in the synthetic routes, most manufacturing techniques are complex and only suitable for one type of particle. Interestingly, radiation chemistry, i.e., the use of ionizing radiation from radioisotopes and accelerators to induce nanomaterials or chemical changes in materials, has proven to be a versatile tool for controlled manufacturing of both organic and inorganic nanoparticles. The advantages of using radiation chemistry for this purpose are many, such as low energy consumption, minimal use of potentially harmful chemicals and simple production schemes. For medical applications one more advantage is that the material can be sterile as manufactured. Radiation-induced synthesis can be carried out in aqueous systems, which minimizes the use of organic solvents and the need for separation and purification of the final product. The radiation chemistry of water is well known, as are the various ways of fine-tuning the reactivity of the system towards a desired target by adding different solutes. This, in combination with the controllable and adjustable irradiation process parameters, makes the technique superior to most other chemical methods. In this review, we discuss the fundamentals of radiation chemistry and radiation-induced synthesis of nanoparticles in aqueous solutions. The impact of dose and

  16. DESIGN OF ROBOTIC COLONIZER CONTROL SYSTEM FOR AQUEOUS ENVIRONMENT

    Directory of Open Access Journals (Sweden)

    C.VENKATESH

    2013-05-01

    Full Text Available Now a days there is a huge interest on underwater communication systems for various applications in order to explore aqueous environments. Intelligent robots and cooperative multi- agent robotic systems can be very efficient tools to speed up search and research operations in remote areas. Robots are also useful to do jobs inareas and in situations that are hazardous for human, they can go anywhere that is not reachable my humans and can go into gaps and move trough small holes that are impossible for humans and even trained dogs. in this paper, a wireless underwater mobile robot system is designed in order to study the behavior of artemia group. anew idea has been presented for underwater mobile robot system which is consists of two parts, first is the underwater mechanical robot and the second is ZigBee wireless based mobile robot which controls and moves the first part. by this system different patterns motion control (linear, circular, zigzag, etc. has been performed and proved the ability to control group of robot by controlling the group of artemia and monitoring the underwater mobile robot control with the help of water proof RF wireless camera and also explore the details present around the mobile robot

  17. A green deep eutectic solvent-based aqueous two-phase system for protein extracting

    International Nuclear Information System (INIS)

    Highlights: • A strategy for the protein purification with a deep eutectic solvent(DES)-based aqueous two-phase system. • Choline chloride-glycerin DES was selected as the extraction solvent. • Bovine serum albumin and trypsin were used as the analytes. • Aggregation phenomenon was detected in the mechanism research. - Abstract: As a new type of green solvent, deep eutectic solvent (DES) has been applied for the extraction of proteins with an aqueous two-phase system (ATPS) in this work. Four kinds of choline chloride (ChCl)-based DESs were synthesized to extract bovine serum albumin (BSA), and ChCl-glycerol was selected as the suitable extraction solvent. Single factor experiments have been done to investigate the effects of the extraction process, including the amount of DES, the concentration of salt, the mass of protein, the shaking time, the temperature and PH value. Experimental results show 98.16% of the BSA could be extracted into the DES-rich phase in a single-step extraction under the optimized conditions. A high extraction efficiency of 94.36% was achieved, while the conditions were applied to the extraction of trypsin (Try). Precision, repeatability and stability experiments were studied and the relative standard deviations (RSD) of the extraction efficiency were 0.4246% (n = 3), 1.6057% (n = 3) and 1.6132% (n = 3), respectively. Conformation of BSA was not changed during the extraction process according to the investigation of UV–vis spectra, FT-IR spectra and CD spectra of BSA. The conductivity, dynamic light scattering (DLS) and transmission electron microscopy (TEM) were used to explore the mechanism of the extraction. It turned out that the formation of DES–protein aggregates play a significant role in the separation process. All the results suggest that ChCl-based DES-ATPS are supposed to have the potential to provide new possibilities in the separation of proteins

  18. A green deep eutectic solvent-based aqueous two-phase system for protein extracting

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Kaijia; Wang, Yuzhi, E-mail: wyzss@hnu.edu.cn; Huang, Yanhua; Li, Na; Wen, Qian

    2015-03-15

    Highlights: • A strategy for the protein purification with a deep eutectic solvent(DES)-based aqueous two-phase system. • Choline chloride-glycerin DES was selected as the extraction solvent. • Bovine serum albumin and trypsin were used as the analytes. • Aggregation phenomenon was detected in the mechanism research. - Abstract: As a new type of green solvent, deep eutectic solvent (DES) has been applied for the extraction of proteins with an aqueous two-phase system (ATPS) in this work. Four kinds of choline chloride (ChCl)-based DESs were synthesized to extract bovine serum albumin (BSA), and ChCl-glycerol was selected as the suitable extraction solvent. Single factor experiments have been done to investigate the effects of the extraction process, including the amount of DES, the concentration of salt, the mass of protein, the shaking time, the temperature and PH value. Experimental results show 98.16% of the BSA could be extracted into the DES-rich phase in a single-step extraction under the optimized conditions. A high extraction efficiency of 94.36% was achieved, while the conditions were applied to the extraction of trypsin (Try). Precision, repeatability and stability experiments were studied and the relative standard deviations (RSD) of the extraction efficiency were 0.4246% (n = 3), 1.6057% (n = 3) and 1.6132% (n = 3), respectively. Conformation of BSA was not changed during the extraction process according to the investigation of UV–vis spectra, FT-IR spectra and CD spectra of BSA. The conductivity, dynamic light scattering (DLS) and transmission electron microscopy (TEM) were used to explore the mechanism of the extraction. It turned out that the formation of DES–protein aggregates play a significant role in the separation process. All the results suggest that ChCl-based DES-ATPS are supposed to have the potential to provide new possibilities in the separation of proteins.

  19. Preparation of CuO nanoparticles by metal salt-base reaction in aqueous solution and their metallic bonding property

    International Nuclear Information System (INIS)

    This article describes a method for preparing CuO nanoparticles in aqueous solution, and a demonstration of feasibility of metallic bonding with the use of the CuO particles. Colloid solution of CuO nanoparticles was prepared from Cu(NO3)2 aqueous solution (0.01 M) and NaOH aqueous solution (0.019 M) at 5–80 °C. Leaf-like aggregates with an average size of 567 nm composed of CuO nanoparticles were produced at 20 °C. The size of leaf-like aggregates decreased with increasing reaction temperature. Metallic copper discs could be bonded using the CuO nanoparticles under annealing at 400 °C and pressurizing at 1.2 MPa for 5 min in H2 gas. A shear strength required for separating the bonded discs was 25.4 MPa for the CuO nanoparticles prepared at 20 °C, whose aggregates were the largest among the CuO particles examined. These results indicated that the formation of leaf-like aggregates of CuO nanoparticles led to efficient metallic bonding.

  20. ENVIRONMENTAL TECHNOLOGY VERIFICATION REPORT; ULTRASONIC AQUEOUS CLEANING SYSTEMS, SMART SONIC CORPORATION, SMART SONIC

    Science.gov (United States)

    This report is a product of the U.S. EPA's Environmental Technoloy Verification (ETV) Program and is focused on the Smart Sonics Ultrasonic Aqueous Cleaning Systems. The verification is based on three main objectives. (1) The Smart Sonic Aqueous Cleaning Systems, Model 2000 and...

  1. Effects of an aqueous leaf extract of Sansevieria senegambica Baker on plasma biochemistry and haematological indices of salt-loaded rats

    Directory of Open Access Journals (Sweden)

    Jude C. Ikewuchi

    2011-11-01

    Full Text Available The effects of an aqueous extract of the leaves of Sansevieria senegambica on plasma marker enzymes, plasma chemistry and the haematological profile of salt-loaded rats were studied. The control group received only a commercial feed, whilst the four test groups received a diet consisting of the commercial feed and salt, although the reference treatment group was reverted to the normal feed at the end of 6 weeks. The extract was orally administered daily at 150 mg/kg or 200 mg/kg body weight to two test groups, respectively; whilst the test control, reference and control groups received equivalent volumes of water by the same route. The extract had no negative effects on markers of liver and kidney functions, but it did produce leukocytosis, significantly increased (p < 0.05 plasma calcium and potassium levels and significantly decreased (p < 0.05 plasma sodium and chloride levels in the test animals compared to the test control animals. This result supports the traditional use of Sansevieria senegambica in the management of hypertension, whilst suggesting that the extract may be a potassium-sparing diuretic whose mechanism of antihypertensive action may be achieved through alteration of plasma sodium and potassium balances, or through calcium-mediated changes in vascular muscle tone.

  2. Reticulation of Aqueous Polyurethane Systems Controlled by DSC Method

    Directory of Open Access Journals (Sweden)

    Jakov Stamenkovic

    2006-06-01

    Full Text Available The DSC method has been employed to monitor the kinetics of reticulation ofaqueous polyurethane systems without catalysts, and with the commercial catalyst of zirconium(CAT®XC-6212 and the highly selective manganese catalyst, the complex Mn(III-diacetylacetonemaleinate (MAM. Among the polyol components, the acrylic emulsions wereused for reticulation in this research, and as suitable reticulation agents the water emulsiblealiphatic polyisocyanates based on hexamethylendoisocyanate with the different contents ofNCO-groups were employed. On the basis of DSC analysis, applying the methods of Kissinger,Freeman-Carroll and Crane-Ellerstein the pseudo kinetic parameters of the reticulation reactionof aqueous systems were determined. The temperature of the examination ranged from 50oC to450oC with the heat rate of 0.5oC/min. The reduction of the activation energy and the increaseof the standard deviation indicate the catalytic action of the selective catalysts of zirconium andmanganese. The impact of the catalysts on the reduction of the activation energy is thestrongest when using the catalysts of manganese and applying all the three afore-said methods.The least aberrations among the stated methods in defining the kinetic parameters wereobtained by using the manganese catalyst.

  3. Influence of Salts on the Partitioning of 5-Hydroxymethylfurfural in Water/MIBK.

    Science.gov (United States)

    Mohammad, Sultan; Held, Christoph; Altuntepe, Emrah; Köse, Tülay; Sadowski, Gabriele

    2016-04-28

    This study investigates the influence of electrolytes on the performance of extracting 5-hydroxymethylfurfural (HMF) from aqueous media using methyl isobutyl ketone (MIBK). For that purpose, liquid-liquid phase equilibria (LLE) of quaternary systems containing HMF, water, MIBK and salts were measured at atmospheric pressure and 298.15 K. The salts under investigation were composed of one of the anions NO(3-), SO4(2-), Cl(-), or CH3COO(-) and of one of the alkali cations Li(+), Na(+), or K(+). On the basis of these LLE data, the partition coefficient of HMF between the aqueous and the MIBK phase KHMF was determined. It could be shown that KHMF significantly depends on the kind and concentration of the added salt. Weak electrolytes (e.g., sulfates, acetates) caused salting-out, whereas nitrates caused salting-in of HMF to the aqueous phase. Unexpectedly, LiCl caused salting-out at low LiCl concentrations and salting-in at LiCl concentrations higher than 3 mol/kgH2O. The model electrolyte perturbed-chain SAFT (ePC-SAFT) was used to predict the salt influence on the LLE in the quaternary systems water/MIBK/HMF/salt in good agreement with the experimental data. On the basis of ePC-SAFT, it could be concluded that the different salting-out/salting-in behavior of the various salts is mainly caused by their different tendency to form ion pairs in aqueous solutions. PMID:27027570

  4. System Requirements Document for the Molten Salt Reactor Experiment

    Energy Technology Data Exchange (ETDEWEB)

    Aigner, R.D.

    2000-04-01

    The purpose of the conversion process is to convert the {sup 233}U fluoride compounds that are being extracted from the Molten Salt Reactor Experiment (MSRE) equipment to a stable oxide for long-term storage at Bldg. 3019.

  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. Triton X-100 as a complete liquid scintillation cocktail for counting aqueous solutions and ionic nutrient salts

    International Nuclear Information System (INIS)

    Triton X-100, used alone, was found to act as a complete liquid scintillation cocktail. Triton X-100 acted as a scintillator and the effect was not due to Cerenkov radiation. A variety of other commercially available surfactants also acted as scintillators, but with different levels of efficiency. Triton X-100/water combinations were suitable for counting aqueous solutions of 33P and 86Rb and the count rate was stable over extended periods of time. Triton X-100/toluene combinations also yielded high counting efficiencies. Triton X-100 was more sensitive to quenching than standard cocktails containing fluors. (author)

  7. An improvement study on the closed chamber distillation system for recovery of renewable salts from salt wastes containing radioactive rare earth compounds

    International Nuclear Information System (INIS)

    In this paper, an improvement study on the closed chamber distillation system for recovery of renewable salts from salt wastes containing radioactive rare earth compounds was performed to determine optimum operating conditions. It was very important to maintain the pressure in the distillation chamber below 10 Torr for a high efficiency (salt recovery >99 %) of the salt distillation. This required increasing the salt vaporization and condensation rates in the distillation system. It was confirmed that vaporization and condensation rates could be improved controlling the given temperature of top of the condensation chamber. In the distillation tests of the salt wastes containing rare earth compounds, the operation time at a given temperature was greatly reduced changing the given temperature of top of the condensation chamber from 780 to 700 deg C. (author)

  8. Aqueous Two Phase System Assisted Self-Assembled PLGA Microparticles

    Science.gov (United States)

    Yeredla, Nitish; Kojima, Taisuke; Yang, Yi; Takayama, Shuichi; Kanapathipillai, Mathumai

    2016-06-01

    Here, we produce poly(lactide-co-glycolide) (PLGA) based microparticles with varying morphologies, and temperature responsive properties utilizing a Pluronic F127/dextran aqueous two-phase system (ATPS) assisted self-assembly. The PLGA polymer, when emulsified in Pluronic F127/dextran ATPS, forms unique microparticle structures due to ATPS guided-self assembly. Depending on the PLGA concentration, the particles either formed a core-shell or a composite microparticle structure. The microparticles facilitate the simultaneous incorporation of both hydrophobic and hydrophilic molecules, due to their amphiphilic macromolecule composition. Further, due to the lower critical solution temperature (LCST) properties of Pluronic F127, the particles exhibit temperature responsiveness. The ATPS based microparticle formation demonstrated in this study, serves as a novel platform for PLGA/polymer based tunable micro/nano particle and polymersome development. The unique properties may be useful in applications such as theranostics, synthesis of complex structure particles, bioreaction/mineralization at the two-phase interface, and bioseparations.

  9. Salt fluxes in a complex river mouth system of Portugal.

    Directory of Open Access Journals (Sweden)

    Nuno Vaz

    Full Text Available Measurements of velocity and salinity near the mouth and head of the Espinheiro channel (Ria de Aveiro lagoon, Portugal are used to study the local variation of physical water properties and to assess the balance, under steady conditions, between the seaward salt transport induced by river discharge and the landward dispersion induced by various mixing mechanisms. This assessment is made using data sampled during complete tidal cycles. Under the assumption that the estuarine tidal channel is laterally homogeneous and during moderate tidal periods (except for one survey, currents and salinity data were decomposed into various spatial and temporal means and their deviations. Near the channel's mouth, the main contributions to the salt transport are the terms due to freshwater discharge and the tidal correlation. Near the channel's head, this last term is less important than the density driven circulation, which is enhanced by the increase in freshwater discharge. The remaining terms, which are dependent on the deviations from the mean depth have a smaller role in the results of salt transport. The computed salt transport per unit width of a section perpendicular to the mean flow is in close agreement to the sum of the advective and dispersive terms (within or very close to 12%. An imbalance of the salt budget across the sections is observed for all the surveys. Considerations are made on how this approach can inform the management of hazardous contamination and how to use these results to best time the release of environmental flows during dry months.

  10. 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.

  11. Influence of cation nature of dialkyl phosphoric acid salts on stratification and interphase tension of extraction systems

    International Nuclear Information System (INIS)

    The influence of cation nature on interphase surface activity of DBPA salts in the system: n-dodecane-MeOH solution, where Me-Li+, Na+, K+, Cs+, NH4+, has been studied. It is shown that adsorption work practically does not vary in the series of equimolar solutions of the above-mentioned hydroxides and increases with hydroxide concentration growth in aqueous phase for all the cations mentioned, except NH4+. Area occupied by surfactant molecules in the interface increases insignificantly with the growth of cation hydration degree when passing from K+ to Li+. Stratification of extractant irradiated by the dose of 5.4x104 Gy and non-irradiated one in system with aqueous solutions of MeOH is investigated. It is ascertained that stratification rates are determined by the factors affecting the distribution in the system of ionogenic surfactants-decomposition products of extractant and diluent, as well as by the difference in the phase densities and, to a less degree, by the values of interphase tension. The highest stratification rates are observed in systems with LiOH and CsOH

  12. Two-phase aqueous micellar systems: an alternative method for protein purification

    Directory of Open Access Journals (Sweden)

    Rangel-Yagui C. O.

    2004-01-01

    Full Text Available Two-phase aqueous micellar systems can be exploited in separation science for the extraction/purification of desired biomolecules. This article reviews recent experimental and theoretical work by Blankschtein and co-workers on the use of two-phase aqueous micellar systems for the separation of hydrophilic proteins. The experimental partitioning behavior of the enzyme glucose-6-phosphate dehydrogenase (G6PD in two-phase aqueous micellar systems is also reviewed and new results are presented. Specifically, we discuss very recent work on the purification of G6PD using: i a two-phase aqueous micellar system composed of the nonionic surfactant n-decyl tetra(ethylene oxide (C10E4, and (ii a two-phase aqueous mixed micellar system composed of C10E4 and the cationic surfactant decyltrimethylammonium bromide (C10TAB. Our results indicate that the two-phase aqueous mixed (C10E4/C10TAB micellar system can improve significantly the partitioning behavior of G6PD relative to that observed in the two-phase aqueous C10E4 micellar system.

  13. Radiation Effects of Hydroxypropyl Methylcellulose Phthalate in Aqueous System

    International Nuclear Information System (INIS)

    Natural polymers and their derivatives were regarded as radiation degradation type polymer for a long time. However, since the successful crosslinking of CMC in so call paste-like status, quite a few natural polymer derivatives were found to be capable of crosslinking via irradiation. Hydroxypropyl methylcellulose phthalate (HPMCP) is water-insoluble cellulose ether with phthalate substitution and is widely used in the pharmaceutical industry due to its resistance to hydrolysis. It was found to be radiation-crosslinkable in basic solution and some organic solvents, but the gelation dose (Dg) was rather high (ca. 50 kGy). In this study, effects of two crosslinkers, i.e. methyl N, N-bis-acrylamide (bis) and ethyleneglycol dimethacrylate (EGDMA), on the accelerating of radiation crosslinking of HPMCP was studied. Intrinsic viscosities of HPMCP solution with various concentrations (10-20%) irradiated at different dose were determined to find the critical concentration for crosslinking of HPMCP and to understand the behavior of HPMCP solution before gel formation. Ion-specific swelling behavior of HPMCP hydrogel in various kinds of salt solutions was investigated to elucidate the interactions between different ion species and HPMCP. The results showed that (1) bis was apparently effective for accelerating the crosslinking of HPMCP; intrinsic viscosities of 20% HPMCP was found to be increased with increasing absorbed dose and vice versa for 10% HPMCP, implying that in paste-like status HPMCP followed crosslinking mechanism even before the formation of hydrogel; ion-specific swelling of HPMCP hydrogel without ion-exchange treatment was in good accordance with normal polyelectrolyte hydrogel except in high concentration KF solution. These results will be valuable for the processing and designing of HPMCP-based controlled release system

  14. Nuclear Hybrid Energy System: Molten Salt Energy Storage (Summer Report 2013)

    Energy Technology Data Exchange (ETDEWEB)

    Piyush Sabharwall; Michael George mckellar; Su-Jong Yoon

    2013-11-01

    Effective energy use is a main focus and concern in the world today because of the growing demand for energy. The nuclear hybrid energy system (NHES) is a valuable technical concept that can potentially diversify and leverage existing energy technologies. This report considers a particular NHES design that combines multiple energy systems including a nuclear reactor, energy storage system (ESS), variable renewable generator (VRG), and additional process heat applications. Energy storage is an essential component of this particular NHES because its design allows the system to produce peak power while the nuclear reactor operates at constant power output. Many energy storage options are available, but this study mainly focuses on a molten salt ESS. The primary purpose of the molten salt ESS is to enable the nuclear reactor to be a purely constant heat source by acting as a heat storage component for the reactor during times of low demand, and providing additional capacity for thermo-electric power generation during times of peak electricity demand. This report will describe the rationale behind using a molten salt ESS and identify an efficient molten salt ESS configuration that may be used in load following power applications. Several criteria are considered for effective energy storage and are used to identify the most effective ESS within the NHES. Different types of energy storage are briefly described with their advantages and disadvantages. The general analysis to determine the most efficient molten salt ESS involves two parts: thermodynamic, in which energetic and exergetic efficiencies are considered; and economic. Within the molten salt ESS, the two-part analysis covers three major system elements: molten salt ESS designs (two tank direct and thermocline), the molten salt choice, and the different power cycles coupled with the molten salt ESS. Analysis models are formulated and analyzed to determine the most effective ESS. The results show that the most

  15. Interactions between high salt intake and the musculoskeletal system

    Science.gov (United States)

    Heer, Martina; Frings-Meuthen, Petra; Buehlmeier, Judith; Baecker, Natalie

    Lowering mechanical load like in microgravity is the dominant stimulus leading to muscle and bone loss. However, high dietary salt (NaCl) intake is also considered as a risk factor for osteoporosis and thereby might exacerbate the microgravity induced bone loss. We have recently shown that a very high salt intake leads to an increased bone resorption most likely because of a low-grade metabolic acidosis (Frings-Meuthen et al. JBMR, Epub Dec 2007). A decrease in pH, however, is on the one hand mandatory to activate osteoclast activity, on the other hand it might affect protein metabolism and thereby muscle mass. In head-down bed rest (HDBR) studies physiological adaptation as seen in microgravity is mimicked. In a recent short-term HDBR study of 14 days, we combined high salt intake and low mechanical loading to test if low-grade metabolic acidosis induced by high NaCl intake is an additive stimulus for increased bone resorption and muscle protein loss. The results show that high NaCl intake combined with low mechanical load exaggerates the increase in calcium excretion as well as the rise in bone resorption marker C-telopeptide (both: p ¡ 0.001). Bone alkaline phosphatase, a bone formation marker, was not different according to NaCl intake (p = 0.74). Additionally, the slightly negative nitrogen balance in HDBR ( 0.34 ± 1.2 g/d) was exacerbated 3 fold by high NaCl intake ( 1.34 ± 1.0 g/d; p ¡ 0.001). These results were accompanied by reduced bicarbonate (p = 0.018) and base excess (p = 0.009) concentrations during high salt intake. In conclusion, HDBR and high salt intake cause -like in ambulatory test subjectsa low-grade metabolic acidosis. This may exacerbate bone resorption and nitrogen loss, which may then exaggerate disuse induced bone and muscle loss.

  16. Aqueous two-phase systems: an efficient, environmentally safe and economically viable method for purification of natural dye carmine.

    Science.gov (United States)

    Mageste, Aparecida Barbosa; de Lemos, Leandro Rodrigues; Ferreira, Guilherme Max Dias; da Silva, Maria do Carmo Hespanhol; da Silva, Luis Henrique Mendes; Bonomo, Renata Cristina Ferreira; Minim, Luis Antonio

    2009-11-01

    Partition of the natural dye carmine has been studied in aqueous two-phase systems prepared by mixing aqueous solutions of polymer or copolymer with aqueous salt solutions (Na(2)SO(4) and Li(2)SO(4)). The carmine dye partition coefficient was investigated as a function of system pH, polymer molar mass, hydrophobicity, system tie-line length and nature of the electrolyte. It has been observed that the carmine partition coefficient is highly dependent on the electrolyte nature and pH of the system, reaching values as high as 300, indicating the high potential of the two-phase extraction with ATPS in the purification of carmine dye. The partition relative order was Li(2)SO(4)"Na(2)SO(4). Carmine molecules were concentrated in the polymer-rich phase, indicating an enthalpic specific interaction between carmine and the pseudopolycation, which is formed by cation adsorption along the macromolecule chain. When the enthalpic carmine-pseudopolycation interaction decreases, entropic forces dominate the natural dye-transfer process, and the carmine partitioning coefficient decreases. The optimization of the extraction process was obtained by a central composite face-centered (CCF) design. The CCF design was used to evaluate the influence of Li(2)SO(4) and PEO 1500 concentration and of the pH on the partition coefficient of carmine. The conditions that maximize the partition of carmine into the top phase were determined to be high concentrations of PEO and Li(2)SO(4) and low pH values within the ranges studied. PMID:19800067

  17. Search for a new greener technology for separation of NCA 97Ru from bulk Nb: ionic liquid based aqueous biphasic system

    International Nuclear Information System (INIS)

    Ionic-liquid (IL) based aqueous biphasic system was developed for the separation of no-carrier-added (NCA) 97Ru from bulk niobium target for the first time as greener separation technology. Room temperature ionic liquid, 1-butyl-3-methylimidazolium Chloride ((Bmim)Cl) against K2HPO4 as salt rich phase was employed to construct this IL-ABS system. In the typical experimental condition, 50 % NCA 97Ru was extracted into the ionic liquid phase without any contamination of Nb, with a separation factor of 5.3x103. (author)

  18. Initiation of nuclear reactions under laser irradiation of Au nanoparticles in the aqueous solution of Uranium salt

    CERN Document Server

    Simakin, A V

    2010-01-01

    Laser exposure of suspension of either gold or palladium nanoparticles in aqueous solutions of UO2Cl2 of natural isotope abundance was experimentally studied. Picosecond Nd:YAG lasers at peak power from 1011 to 1013 W/cm2 at the wavelength of 1064 and 355 nm were used as well as a visible-range Cu vapor laser at peak power of 1010 W/cm2. The composition of colloidal solutions before and after laser exposure was analyzed using atomic absorption and gamma spectroscopy between 0.06 and 1 MeV range of photon energy. A real-time gamma-spectroscopy was used to characterize the kinetics of nuclear reactions during laser exposure. It was found that laser exposure initiated nuclear reactions involving both 238U and 235U nuclei via different channels in H2O and D2O. The influence of saturation of both the liquid and nanoparticles by gaseous H2 and D2 on the kinetics of nuclear transformations was found. Possible mechanisms of observed processes are discussed.

  19. Main Experimental Results of ISTC-1606 for Recycling and Transmutation in Molten Salt Systems

    Energy Technology Data Exchange (ETDEWEB)

    Ignatiev, Victor; Feynberg, Olga; Merzlyakov, Aleksandr; Surenkov, Aleksandr [Russian Research Center - Kurchatov Institute, Kurchatov sq. 1, Moscow, RF, 123182 (Russian Federation); Subbotin, Vladimir; Zakirov, Raul; Toropov, Andrey; Panov, Aleksandr [Russian Federal Nuclear Center - Institute of Technical Physics, Snezhinsk (Russian Federation); Afonichkin, Valery [Institute of High-Temperature Electrochemistry, Ekaterinburg (Russian Federation)

    2008-07-01

    To examine and demonstrate the feasibility of molten salt reactors (MSR) to reduce long lived waste toxicity and to produce efficiently electricity in closed fuel cycle, some national and international studies were initiated last years. In this paper main focus is placed on experimental evaluation of single stream Molten Salt Actinide Recycler and Transmuter (MOSART) system fuelled with different compositions of plutonium plus minor actinide trifluoride (AnF{sub 3}) from LWR spent nuclear fuel without U-Th support. This paper summarizes main experimental results of ISTC-1606 related to physical and chemical properties of fuel salt, container materials for fuel circuit, and fuel salt clean up of MOSART system. As result of ISTC-1606 studies claim is made, that the {sup 7}Li,Na,Be/F and {sup 7}Li,Be/F solvents selected for primary system appear to resolve main reactor physics, thermal hydraulics, materials compatibility, fuel salt clean up and safety problems as applied to the MOSART concept development. The created experimental facilities and the database on properties of fuel salt mixtures and container materials are used for a choice and improvement fuel salts and coolants for new applications of this high temperature technology for sustainable nuclear power development. (authors)

  20. Main Experimental Results of ISTC-1606 for Recycling and Transmutation in Molten Salt Systems

    International Nuclear Information System (INIS)

    To examine and demonstrate the feasibility of molten salt reactors (MSR) to reduce long lived waste toxicity and to produce efficiently electricity in closed fuel cycle, some national and international studies were initiated last years. In this paper main focus is placed on experimental evaluation of single stream Molten Salt Actinide Recycler and Transmuter (MOSART) system fuelled with different compositions of plutonium plus minor actinide trifluoride (AnF3) from LWR spent nuclear fuel without U-Th support. This paper summarizes main experimental results of ISTC-1606 related to physical and chemical properties of fuel salt, container materials for fuel circuit, and fuel salt clean up of MOSART system. As result of ISTC-1606 studies claim is made, that the 7Li,Na,Be/F and 7Li,Be/F solvents selected for primary system appear to resolve main reactor physics, thermal hydraulics, materials compatibility, fuel salt clean up and safety problems as applied to the MOSART concept development. The created experimental facilities and the database on properties of fuel salt mixtures and container materials are used for a choice and improvement fuel salts and coolants for new applications of this high temperature technology for sustainable nuclear power development. (authors)

  1. Searching for an idealistic nuclear energy system. The thorium molten-salt nuclear energy synergetic system

    International Nuclear Information System (INIS)

    The solar-based energy should become a global major one at the end of this century. The intermediate between fossil and solar energies has to be filled by the fission energy. For the decisive improvement of its safety, radioactive-waste and plutonium issues, the Thorium Molten-Salt Nuclear Energy Synergetic System should be established by the use of fluid-fuel of 7LiF-BeF2-based molten fluoride salt, as a triple functional medium for nuclear-reaction, heat-transfer and chemical-process without radiation-damage. This system is composed of simple and economical fuel-self-sustaining small power reactors and Accelerator Molten-Salt Breeders for spallation breeding. The economical extinction of radioactive-wastes will be achieved by using excess fuel (neutron) at the phase-out period of this system near the end of this century. This technology will be essential for solving global environmental and poverty issues and for the complete abolition of nuclear weapons. (author)

  2. Design of the distributed control system for HTS molten salt test loop

    International Nuclear Information System (INIS)

    Background: Experimental Physics and Industrial Control System (EPICS) is the distributed control system software which is commonly used in large-scale experimental physics facilities. Purpose: We wish to apply it into the field of molten salt reactor relevant process control, e.g. HTS 1st test loop of thorium-based molten salt reactor (TMSR), which is characterized by heating, circulation, cooling and other process control. Methods: During the development of EPICS based control system, the Simense S7-300 PLC and Yokogawa FA-M3 PLC hardware drivers specification format transformation has been done, to support the Autosave and devIocState plug, and ASYN serial communication between the DTI-1000 reference digital temperature indicator and the EPICS IOC has been developed with the StreamDevice packages, also EDM interface program was modified to support PV control of the 'molten salt flow', 'fans', 'molten salt pump rotation', etc. by dynamic symbols. Results: EPICS based control system achieved the standardized communication of three hardwares with different types, the monitoring and storage of nearly 500 process variables, and the dynamic monitoring of control process. Conclusions: The EPICS-based control system can achieve the molten salt heating, feeding, cooling and other process control of the molten salt test loop. Safety analysis and research of control system requires further efforts to implement. (authors)

  3. Structure and molecular dynamics of sodium dodecylsulfate micelles modified with hydrophilic short-chain imidazolium salts in aqueous solution.

    Science.gov (United States)

    Lin, Jia-Hsien; Hou, Sheng-Shu

    2016-07-15

    This study uses pyrene solubilization and NMR experiments to investigate the effects of two hydrophilic short-chain ionic liquids (ILs), 1-ethyl-3-methylimidazolium tetrafluoroborate (EmimBF4) and 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF4) on the micellization of sodium dodecylsulfate (SDS) in the aqueous phase. The results of the pyrene solubilization experiments indicate that the added short-chain ILs not only promote the micellization of SDS but also modify micelle properties. For NMR studies, the present study focuses on (1) the compositions and spatial arrangements of component molecules and (2) the molecular dynamics of DS(-) in the Rmim-modified SDS micelle. Using pulsed field gradient (PFG) NMR measurements, the composition of the Rmim-modified SDS micelle was calculated by the diffusion data and was found to be correlated with the [SDS]. Two-dimensional nuclear Overhauser effect spectroscopy (2D NOESY) experiments confirm that the 1-alkyl-3-methylimidazolium cation (Rmim(+)) is located inside the Rmim-modified SDS micelle. Corresponding to the microstructure of the Rmim-modified SDS micelle, in terms of (1)H T1 relaxation, the fast motion of SDS α-CH2 and β-CH2 segments are markedly restricted by the attached Rmim(+) to the sulfate group of DS(-), whereas the central carbons and the terminal CH3 group of DS(-) are only slightly affected. The chemical shift analysis indicates that the surface of the Rmim-modified SDS micelle is dehydrated by the absorbed Rmim(+) and becomes more hydrophobic than that of the pure SDS micelle. Insertion of Rmim(+) into the Rmim-modified SDS micelle appears to be driven through the hydrophobic interaction, and it is shown to combine with SDS molecules to constitute the hydrophobic part of the Rmim-modified SDS micelle. PMID:27107206

  4. Aqueous solubility study of salts of benzylamine derivatives and p-substituted benzoic acid derivatives using X-ray crystallographic analysis

    DEFF Research Database (Denmark)

    Parshad, Henrik; Frydenvang, Karla Andrea; Liljefors, Tommy; Sorensen, Henning Osholm; Larsen, Claus

    2004-01-01

    Twenty two p-substituted benzoic acid derivates were used to prepare salts of N-methylbenzylamine (II) and N,N-dimethylbenzylamine (III), respectively. Only five salts of (II) and two salts of (III) were obtained in a crystalline state. The solubility of these salts was orders of magnitude higher...

  5. AQUEOUS BIPHASE EXTRACTION FOR PROCESSING OF FINE COAL

    Energy Technology Data Exchange (ETDEWEB)

    K. Osseo-Asare; X. Zeng

    2002-01-01

    The objective of this research project is to develop an aqueous biphase extraction process for the treatment of fine coals. Aqueous biphase extraction is an advanced separation technology that relies on the ability of an aqueous system consisting of a water-soluble polymer and another component, e.g., another polymer, an inorganic salt, or a nonionic surfactant, to separate into two immiscible aqueous phases. The principle behind the partition of solid particles in aqueous biphase systems is the physicochemical interaction between the solid surface and the surrounding liquid solution. In order to remove sulfur and mineral matter from fine coal with aqueous biphasic extraction, it is necessary to know the partitioning behavior of coal, as well as the inorganic mineral components. Therefore, in this research emphasis was placed on the partitioning behavior of fine coal particles as well as model fine inorganic particles in aqueous biphase systems.

  6. Collection and evaluation of salt mixing data with the real time data acquisition system

    International Nuclear Information System (INIS)

    A minicomputer based real time data acquisition system was designed and built to facilitate data collection during salt mixing tests in mock ups of LMFBR rod bundles. The system represents an expansion of data collection capabilities over previous equipment. It performs steady state and transient monitoring and recording of up to 512 individual electrical resistance probes. Extensive real time software was written to govern all phases of the data collection procedure, including probe definition, probe calibration, salt mixing test data acquisition and storage, and data editing. Offline software was also written to permit data examination and reduction to dimensionless salt concentration maps. Finally, the computer program SUPERENERGY was modified to permit rapid extraction of parameters from dimensionless salt concentration maps. The document describes the computer system, and includes circuit diagrams of all custom built components. It also includes descriptions and listings of all software written, as well as extensive user instructions

  7. Collection and evaluation of salt mixing data with the real time data acquisition system. [LMFBR

    Energy Technology Data Exchange (ETDEWEB)

    Glazer, S.; Chiu, C.; Todreas, N.E.

    1977-09-01

    A minicomputer based real time data acquisition system was designed and built to facilitate data collection during salt mixing tests in mock ups of LMFBR rod bundles. The system represents an expansion of data collection capabilities over previous equipment. It performs steady state and transient monitoring and recording of up to 512 individual electrical resistance probes. Extensive real time software was written to govern all phases of the data collection procedure, including probe definition, probe calibration, salt mixing test data acquisition and storage, and data editing. Offline software was also written to permit data examination and reduction to dimensionless salt concentration maps. Finally, the computer program SUPERENERGY was modified to permit rapid extraction of parameters from dimensionless salt concentration maps. The document describes the computer system, and includes circuit diagrams of all custom built components. It also includes descriptions and listings of all software written, as well as extensive user instructions.

  8. Effects of Water Hardness on Textile Detergency Performance in Aqueous Cleaning Systems.

    Science.gov (United States)

    Gotoh, Keiko; Horibe, Kaori; Mei, Yang; Tsujisaka, Toshiyuki

    2016-01-01

    The effects of water hardness on textile detergency in aqueous solutions were systematically investigated using four surfactants: sodium oleate (OLNa), linear dodecylbenzene sulfonate (LAS), sodium dodecyl sulfate (AS), and polyoxyethylene (10) dodecyl ether (AE). Water hardness was adjusted according to the standard procedure described in IEC 60734:2012. As expected, by adding hardness salts the surface tension of the OLNa solution increased. Surprisingly, the addition of hardness salts lowers the surface tension for the LAS and AS solutions. In the case of the AE solution, hardness salt did not affect the surface tension. A decrease in transmittance and foamability after adding hardness salts was observed for every anionic surfactant solution, indicating that anionic surfactants can combine with divalent ions to form insoluble precipitates. Detergency experiments were performed using cotton plain-woven and towel fabrics soiled with a carbon black and oleic acid mixture. One piece each of untreated and soiled fabric were stacked and placed horizontally in detergent solution with or without hardness salts. As a mechanical action of soil removal, the shaking of 190 spm was applied. Soil removal and redeposition due to washing were evaluated from changes in values of the Kubelka-Munk function for both fabrics. With increasing water hardness, soil removal decreased and redeposition increased. In order of decreasing detergency, the surfactants were as follows: LAS > OLNa ≈ AS > AE. The results indicate that precipitates, formed by reaction of LAS or AS with hardness salts, are strongly adsorbed on the water surface because of their hydrophobicity, but they have no detergency power. The field emission scanning electron microscopic observation and X-ray photoelectron spectroscopic analysis showed that Ca(LAS)2 precipitation clung to fiber surfaces, and remained on the surfaces after washing. Significant changes in the cotton fabric due to washing were observed in

  9. Partition behavior of surfactants, butanol, and salt during application of density-modified displacement of dense non-aqueous phase liquids.

    Science.gov (United States)

    Damrongsiri, S; Tongcumpou, C; Sabatini, D A

    2013-03-15

    Density-modified displacement (DMD) is a recent approach for removal of trapped dense NAPL (DNAPL). In this study, butanol and surfactant are contacted with the DNAPL to both reduce the density as well as release the trapped DNAPL (perchloroethylene: PCE). The objective of the study was to determine the distribution of each component (e.g., butanol, surfactant, water, PCE) between the original aqueous and PCE phases during the application of DMD. The results indicated that the presence of the surfactant increased the amount of n-butanol required to make the NAPL phase reach its desired density. In addition, water and anionic surfactant were found to partition along with the BuOH into the PCE phase. The water also found partitioned to reverse micelles in the modified phase. Addition of salt was seen to increase partitioning of surfactant to BuOH containing PCE phase. Subsequently, a large amount of water was solubilized into reverse micelles which lead to significantly increase in volume of the PCE phase. This work thus demonstrates the role of each component and the implications for the operation design of an aquifer treatment using the DMD technique. PMID:23385206

  10. Selection of Xenobiotic-Degrading Microorganisms in a Biphasic Aqueous-Organic System

    OpenAIRE

    Ascon-Cabrera, Miguel; Lebeault, Jean-Michel

    1993-01-01

    Microbial selection on mixtures of chlorinated and nonchlorinated compounds that are poorly soluble in water and/or toxic to growing microbial cells was examined in both biphasic aqueous-organic and monophasic aqueous systems. A biphasic system in which silicone oil was used as the organic phase permitted the acceleration of acclimation, leading to rapid selection and to an increase in xenobiotic compound degradation. In contrast, acclimation, selection, and degradation were very slow in the ...

  11. Salt Fluxes in a Complex River Mouth System of Portugal

    OpenAIRE

    Vaz, Nuno; Lencart e Silva, João D.; Dias, João Miguel

    2012-01-01

    Measurements of velocity and salinity near the mouth and head of the Espinheiro channel (Ria de Aveiro lagoon, Portugal) are used to study the local variation of physical water properties and to assess the balance, under steady conditions, between the seaward salt transport induced by river discharge and the landward dispersion induced by various mixing mechanisms. This assessment is made using data sampled during complete tidal cycles. Under the assumption that the estuarine tidal channel is...

  12. Design of a passive residual heat removal system for the FUJI-233Um molten salt reactor system

    International Nuclear Information System (INIS)

    Highlights: • A passive decay heat removal system for a small molten salt reactor is analyzed. • The system uses water as a coolant and an air cooler as final heat sink. • If the diameter of the coolant pipes is chosen correctly, problems of thermal shock can be avoided. • Safe cooling for a period of at least 10 days can be achieved. • The possibility of draining the primary system is an important safety feature of molten salt reactors. - Abstract: This paper discusses the design and analysis of a passive decay heat removal system for a Molten Salt Reactor (MSR) of 450 MWth. Following the disaster at the Fukushima-1 nuclear power station, it is clear that the public will demand improved safety performance if nuclear power is to be accepted as a sustainable source of CO2-free energy. In this scope, thorium-based MSRs have very promising properties in the area of passive safety, resource availability and proliferation resistance. Molten Salt Reactor (MSR) systems can be equipped with an emergency salt drain tank. Under any severe accident, all the fuel salt can be drained by gravity into the drain tank, thus, the primary system can be safely emptied of fissile materials and fission products. The ultimate safety can be assured by the integrity of the fuel salt in the drain tank or in other words, the capability of residual heat removal from the fuel salt in the drain tank. From this point of view, we investigated the feasibility of a passive residual heat removal system for the drain tank of an MSR (FUJI-233Um of 450 MWth). We concluded that a system comprising a large drain tank and 60, large-diameter coolant tubes can withstand the thermal shock due to the hot fuel salt, and therefore we conclude that system is feasible

  13. The role of cover crops in irrigated systems: Soil salinity and salt leaching

    OpenAIRE

    Gabriel Pérez, José Luis; Almendros García, Patricia; Hontoria Galan, Monica; Quemada Saenz-Badillos, Miguel

    2012-01-01

    Soil salinity and salt leaching are a risk for sustainable agricultural production in many irrigated areas. This study was conducted over 3.5 years to determine how replacing the usual winter fallow with a cover crop (CC) affects soil salt accumulation and salt leaching in irrigated systems. Treatments studied during the period between summer crops were: barley (Hordeum vulgare L.), vetch (Vicia villosa L.) and fallow. Soil water content was monitored daily to a depth of 1.3 m and used with t...

  14. Enhancing productivity of salt affected soils through crops and cropping system

    International Nuclear Information System (INIS)

    The reclamation of salt affected soils needs the addition of soil amendment and enough water to leach down the soluble salts. The operations may also include other simple agronomic techniques to reclaim soils and to know the crops and varieties that may be grown and other management practices which may be followed on such soils (Khan, 2001). The choice of crops to be grown during reclamation of salt affected soils is very important to obtain acceptable yields. This also decides cropping systems as well as favorable diversification for early reclamation, desirable yield and to meet the other requirements of farm families. In any salt affected soils, the following three measures are adopted for reclamation and sustaining the higher productivity of reclaimed soils. 1. Suitable choice of crops, forestry and tree species; 2. Suitable choice of cropping and agroforestry system; 3. Other measures to sustain the productivity of reclaimed soils. (author)

  15. Ionic liquids based aqueous biphasic systems: Effect of the alkyl chains in the cation versus in the anion

    International Nuclear Information System (INIS)

    Highlights: • Alkyl-3-methylimidazolium alkylsulfonate ILs for implemention of aqueous biphasic systems. • Study of the effect of alkyl chain length and position on ILs hydrophobicity. • Evaluation of ILs extractive power on L-tryptophan aqueous solutions. • The alkyl chain in the anion contributes more to the hydrophobicity of the IL. • Less hydrophobic ILs have the better extraction coefficients for L-tryptophan. -- Abstract: The use of alkyl-3-methylimidazolium alkylsulfonate ionic liquids for implementing aqueous biphasic systems is studied in this work for the first time. The ability of high charge density inorganic salts, such as K3PO4, to promote phase segregation in aqueous solutions containing the ionic liquids 1,3-dimethylimidazolium methylsulfonate ([C1mim][C1SO3]), 1-ethyl-3-methylimidazolium hexylsulfonate ([C2mim][C6SO3]), 1-ethyl-3-methylimidazolium butylsulfonate ([C2mim][C4SO3]), 1-butyl-3-methylimidazolium methylsulfonate ([C4mim][C1SO3]), 1-butyl-3-methylimidazolium ethylsulfonate ([C4mim][C2SO3]), 1-pentyl-3-methylimidazolium methylsulfonate ([C5mim][C1SO3]), 1-hexyl-3-methylimidazolium methylsulfonate ([C6mim][C1SO3]) and 1-hexyl-3-methylimidazolium ethylsulfonate ([C6mim][C2SO3]) was experimentally determined at 298.15 K and atmospheric pressure. In general, the hydrophobicity of the ionic liquids studied is affected by the increase of the alkyl chain length. However, the position of the alkyl chain, whether in the cation or in the anion affects in a different way the lipophilic effect of the ionic liquid. Two ionic liquids with the same number of carbon atoms, the one with a longer chain in the anion is the more hydrophobic. Furthermore, four ionic liquids were chosen to extract the aminoacid L-tryptophan from aqueous solutions. The chain lengths of the anion or cation were fixed and the partition coefficients compared. The extractions, carried out at 298.15 K, showed the good extractive power of these ionic liquids and also that

  16. Extraction of Biomolecules Using Phosphonium-Based Ionic Liquids + K3PO4 Aqueous Biphasic Systems

    OpenAIRE

    Louros, Cláudia L. S.; Cláudio, Ana Filipa M.; Neves, Catarina M. S. S.; Freire, Mara G.; Marrucho, Isabel M.; Jérôme Pauly; Coutinho, João A. P.

    2010-01-01

    Aqueous biphasic systems (ABS) provide an alternative and efficient approach for the extraction, recovery and purification of biomolecules through their partitioning between two liquid aqueous phases. In this work, the ability of hydrophilic phosphonium-based ionic liquids (ILs) to form ABS with aqueous K3PO4 solutions was evaluated for the first time. Ternary phase diagrams, and respective tie-lines and tie-lines length, formed by distinct phosphonium-based ILs, water, and K3PO4 at 298 K, we...

  17. Global nuclear energy system-- thorium molten-salt nuclear energy synergetics

    International Nuclear Information System (INIS)

    A simple rational thorium (Th) breeding fuel cycle system, the Thorium Molten-Salt Nuclear Energy Synergetics [THORIMS-NES], composed of simple power stations [utility facility] and fissile producers [process facility], is proposed to establish the essential improvement in issues of safety, power-size flexibility, anti-terrorism and radio-waste, economy, etc. securing the simple operation, maintenance and chemical processing. The design study of small Molten-Salt Reactor, FUJI-II, was performed from 1983, and it showed that it would have a fuel self-sustaining character even not only in a small size, 350MWth-155MWe, but also in the conditions of no core-graphite exchange and no continuous chemical processing, except Kr, Xe and T removal. FUJI-II will be effectively able to incinerate the trans-U elements in the rate of ca.50 kg/y, by replacing about one-third of standard 233U fissile. The fissile producers were studied since 1980 and proposed the Accelerator Molten-Salt Breeder [AMSB], as one of the most promising one, which held a target salt containing 0.5 mol % 233UF4 produced by the spallation of Th or U nuclei in salt and 1 GeV proton. The target salt can be supplied straightly to the fuel tank of Molten-Salt Reactors (FUJI). (author). 20 refs., 6 figs., 3 tabs

  18. Materials considerations for molten salt accelerator-based plutonium conversion systems

    Energy Technology Data Exchange (ETDEWEB)

    DeVan, J.H.; DiStefano, J.R.; Eatherly, W.P.; Keiser, J.R.; Klueh, R.L.

    1994-12-31

    A Molten-Salt Reactor Program for power applications was initiated at the Oak Ridge National Laboratory in 1956. In 1965 the Molten Salt Reactor Experiment (MSRE) went critical and was successfully operated for several years. Operation of the MSRE revealed two deficiencies in the Hastelloy N alloy that had been developed specifically for molten-salt systems. The alloy embrittled at elevated temperatures as a result of exposure to thermal neutrons (radiation damage) and grain boundary embrittlement occurred in materials to fuel salt. Intergranular cracking was found to be associated with fission products, viz. tellurium. An improved Hastelloy N composition was subsequently developed that had better resistance to both of these problems. However, the discovery that fission product cracking could be significantly decreased by making the salt sufficiently reducing offers the prospect of improved compatibility with molten salts containing fission products and resistance to radiation damage in ABC applications. Recommendations are made regarding the types of corrosion tests and mechanistic studies needed to qualify materials for operation with PuF{sub 3}-containing molten salts.

  19. IS MONO SODIUM GLUTAMATE SALT (MSG) HARMFUL TO LIVING SYSTEMS?

    OpenAIRE

    2014-01-01

    Monosodium glutamate (MSG), also known as sodium glutamate, is the sodium salt of glutamic acid, one of the most abundant naturally occurring non-essential amino acids. A widespread and silent killer that’s worse for your health than alcohol, nicotine and many drugs is likely lurking in your kitchen cabinets right now. “It” is monosodium glutamate (MSG), a flavor enhancer that’s known widely as an addition to Chinese food, but that’s actually added to thousands of the foods you and your famil...

  20. Internally consistent thermodynamic data for aqueous species in the system Na-K-Al-Si-O-H-Cl

    Science.gov (United States)

    Miron, George D.; Wagner, Thomas; Kulik, Dmitrii A.; Heinrich, Christoph A.

    2016-08-01

    A large amount of critically evaluated experimental data on mineral solubility, covering the entire Na-K-Al-Si-O-H-Cl system over wide ranges in temperature and pressure, was used to simultaneously refine the standard state Gibbs energies of aqueous ions and complexes in the framework of the revised Helgeson-Kirkham-Flowers equation of state. The thermodynamic properties of the solubility-controlling minerals were adopted from the internally consistent dataset of Holland and Powell (2002; Thermocalc dataset ds55). The global optimization of Gibbs energies of aqueous species, performed with the GEMSFITS code (Miron et al., 2015), was set up in such a way that the association equilibria for ion pairs and complexes, independently derived from conductance and potentiometric data, are always maintained. This was achieved by introducing reaction constraints into the parameter optimization that adjust Gibbs energies of complexes by their respective Gibbs energy effects of reaction, whenever the Gibbs energies of reactant species (ions) are changed. The optimized thermodynamic dataset is reported with confidence intervals for all parameters evaluated by Monte Carlo trial calculations. The new thermodynamic dataset is shown to reproduce all available fluid-mineral phase equilibria and mineral solubility data with good accuracy and precision over wide ranges in temperature (25-800 °C), pressure (1 bar to 5 kbar) and composition (salt concentrations up to 5 molal). The global data optimization process adopted in this study can be readily repeated any time when extensions to new chemical elements and species are needed, when new experimental data become available, or when a different aqueous activity model or equation of state should be used. This work serves as a proof of concept that our optimization strategy is feasible and successful in generating a thermodynamic dataset reproducing all fluid-mineral and aqueous speciation equilibria in the Na-K-Al-Si-O-H-Cl system within

  1. Effects of Na2SO4 or NaCl on sonochemical degradation of phenolic compounds in an aqueous solution under Ar: Positive and negative effects induced by the presence of salts.

    Science.gov (United States)

    Uddin, Md Helal; Nanzai, Ben; Okitsu, Kenji

    2016-01-01

    Sonochemical degradation of 4-chlorophenol, phenol, catechol and resorcinol was studied under Ar at 200 kHz in the absence and presence of Na2SO4 or NaCl. The rates of sonochemical degradation in the absence of salts decreased in the order 4-chlorophenol>phenol>catechol>resorcinol and this order was in good agreement with the order of log P (partition coefficient) value of each phenolic compound. The effects of salts on the rates of sonochemical degradation consisted of no effect or slight negative or positive effects. We discussed these unclear results based on two viewpoints: one was based on the changes in pseudo hydrophobicity and/or diffusion behavior of phenolic compounds and the other was based on the changes in solubility of Ar gas. The measured log P value of each phenolic compound slightly increased with increasing salt concentration. In addition, the dynamic surface tension for 4-chlorophenol aqueous solution in the absence and presence of Na2SO4 or NaCl suggested that phenolic compounds more easily accumulated at the interface region of bubbles at higher salt concentration. These results indicated that the rates of sonochemical degradation should be enhanced by the addition of salts. On the other hand, the calculated Ar gas solubility was confirmed to decrease with increasing salt concentration. The yield of H2O2 formed in the presence of Na2SO4 or NaCl decreased with increasing salt concentration. These results suggested that sonochemical efficiency decreased with decreasing gas amount in aqueous solution: a negative effect of salts was observed. Because negative and positive effects were induced simultaneously, we concluded that the effects of salts on the rates of sonochemical degradation of phenolic compounds became unclear. The products formed from sonochemical degradation of 4-chlorophenol were also characterized by HPLC analysis. The formation of phenol and 4-chloro-1,3-dihydroxy benzene was confirmed and these concentrations were affected by the

  2. Inhibition Effect of Mace Extract Microemulsion on Vitamin C Photooxidation in Aqueous Systems

    Directory of Open Access Journals (Sweden)

    Hasbullah Hasbullah

    2014-01-01

    Full Text Available Photooxidation in food systems cause nutritional losses and produces undesirable flavor, toxic and color compounds, which make foods less acceptable or unacceptable to consumers. The objective of this research was to know the effectiveness of mace extract microemulsion to inhibit vitamin C photooxidation in aqueous systems. Aqueous food systems used are both beverage model system and apple juice beverage, where in each system enriched by 100 ppm vitamin C as substrate and 20 ppm erytrosin as photosensitiser. It is about one percent and two percent of microemulsion that contain mace extract of 0, 500 and 750 ppm were added into each of aqueous food system. Inhibition effect of mace extract microemulsion toward vitamin C photooxidation based on the rate of vitamin C degradation in aqueous food systems that illuminated by fluorescent light with 2000 lux intensity within eight hours. The result indicated the mace extract microemulsion has anti-photooxidation activity and ability to inhibit vitamin C photooxidation in aqueous systems.

  3. Radiation formation of colloidal silver particles in aqueous systems

    Energy Technology Data Exchange (ETDEWEB)

    Cuba, Vaclav [CTU in Prague, Faculty of Nuclear Sciences and Physical Engineering, Brehova 7, 115 19 Prague 1 (Czech Republic)], E-mail: vaclav.cuba@fjfi.cvut.cz; Nemec, Mojmir; Gbur, Tomas; John, Jan; Pospisil, Milan; Mucka, Viliam [CTU in Prague, Faculty of Nuclear Sciences and Physical Engineering, Brehova 7, 115 19 Prague 1 (Czech Republic)

    2010-04-15

    This paper reports on the formation of silver nanoparticles initiated by gamma and UV radiation in various aqueous solutions. Inorganic precursors were used for radiation and/or photochemical reduction of Ag{sup +} ions to a metallic form. The influence of various parameters on the nucleation and formation of colloid particles was studied. Attention was also focused on the composition of the irradiated solution. Aliphatic alcohols were used as scavengers of OH radicals and other oxidizing species. The influence of the stabilizers on the formation and stability of the nanoparticles was studied.

  4. Salt Effect on the Cloud Point Phenomenon of Amphiphilic Drug-Hydroxypropylmethyl Cellulose System

    Directory of Open Access Journals (Sweden)

    Mohd. Sajid Ali

    2014-01-01

    Full Text Available Effect of two amphiphilic drugs (tricyclic antidepressant, nortriptyline hydrochloride (NORT, and nonsteroidal anti-inflammatory drug, sodium salt of ibuprofen (IBF on the cloud point of biopolymer hydroxypropylmethyl cellulose (HPMC was studied. Effect of NaCl was also seen on the CP of HPMC-drug system. CP of HPMC increases uniformly on increasing the (drug. Both drugs, though one being anionic (IBF and other cationic (NORT, affect the CP in almost the same manner but with different extent implying the role of hydrophobicity in the interaction between drug and polymer. Salt affects the CP of the drug in a dramatic way as low concentration of salt was only able to increase the value of the CP, though not affecting the pattern. However, in presence of high concentration of salts, minimum was observed on CP versus (drug plots. Various thermodynamic parameters were evaluated and discussed on the basis of the observed results.

  5. Study of the applicability of non-conventional aqueous two-phase systems in counter-current and centrifugal partition chromatography.

    Science.gov (United States)

    Bezold, Franziska; Goll, Johannes; Minceva, Mirjana

    2015-04-01

    Aqueous two-phase systems composed of imidazolium-based ionic liquids and phosphate salts were evaluated for their applicability in liquid-liquid chromatography. The influence of the nature of ionic liquid anion and cation on the partitioning of bovine serum albumin, lysozyme and myoglobin was investigated. A mixture of K2HPO4 and KH2PO4 in a ratio of 1.82:1 wt/wt was used in all of the tested biphasic systems to adjust the pH to a range of 7-8. The results show that more hydrophobic cations decrease the partition coefficients of the proteins in the biphasic systems and outweigh the effect of the anion on the distribution of the macromolecules. Viscosities and densities of the biphasic systems were in a suitable range for liquid-liquid chromatography. Even though the partition coefficients were too high for a conventional batch operation mode, these aqueous two-phase systems show favorable properties for protein capturing in liquid-liquid chromatographic columns. Additionally, the possible application of ionic liquids as modifiers in polyethylene glycol (PEG)-based aqueous two-phase systems was investigated. It could be demonstrated that ionic liquids alter the partition coefficients of the proteins. PMID:25736304

  6. Study on Salt-Containing Extractive Distillation for the 2-Propanol/Water System

    Institute of Scientific and Technical Information of China (English)

    Fu Jiquan

    2008-01-01

    The salt-containing extractive distillation column and the salt-containing agent recovery column for the 2-propanol/water/ethanediol/KAc system were simulated by the NRTL model and the modified Rose Relaxation method. The simulation results showed that prediction of the salt effect in vapor-liquid equilib-rium and the correlation method (TDCM) of NRTL parameters were suitable for the said system. Four different distillation technology processes were investigated; the results showed that the salt-containing extractive distillation process was the best one. The simulating design of the extractive distillation column was performed under the conditions of different total stage number, feeding location, reflux ratio, amount of mixed agent and concentration of KAc. The results showed that such factors as 17 stages, a feeding location at the 9th stage, a reflux ratio of 1.2, and a mixed agent feeding rate of 1.141 kmol/h, might be the best suited operating conditions. The simulating design was also done for the column for recovering the salt-containing agent. The simulation method of the salt-containing extractive distillation is simple and effective in this work.

  7. Free energetics of carbon nanotube association in aqueous inorganic NaI salt solutions: Temperature effects using all-atom molecular dynamics simulations.

    Science.gov (United States)

    Ou, Shu-Ching; Cui, Di; Wezowicz, Matthew; Taufer, Michela; Patel, Sandeep

    2015-06-15

    In this study, we examine the temperature dependence of free energetics of nanotube association using graphical processing unit-enabled all-atom molecular dynamics simulations (FEN ZI) with two (10,10) single-walled carbon nanotubes in 3 m NaI aqueous salt solution. Results suggest that the free energy, enthalpy and entropy changes for the association process are all reduced at the high temperature, in agreement with previous investigations using other hydrophobes. Via the decomposition of free energy into individual components, we found that solvent contribution (including water, anion, and cation contributions) is correlated with the spatial distribution of the corresponding species and is influenced distinctly by the temperature. We studied the spatial distribution and the structure of the solvent in different regions: intertube, intratube and the bulk solvent. By calculating the fluctuation of coarse-grained tube-solvent surfaces, we found that tube-water interfacial fluctuation exhibits the strongest temperature dependence. By taking ions to be a solvent-like medium in the absence of water, tube-anion interfacial fluctuation shows similar but weaker dependence on temperature, while tube-cation interfacial fluctuation shows no dependence in general. These characteristics are discussed via the malleability of their corresponding solvation shells relative to the nanotube surface. Hydrogen bonding profiles and tetrahedrality of water arrangement are also computed to compare the structure of solvent in the solvent bulk and intertube region. The hydrophobic confinement induces a relatively lower concentration environment in the intertube region, therefore causing different intertube solvent structures which depend on the tube separation. This study is relevant in the continuing discourse on hydrophobic interactions (as they impact generally a broad class of phenomena in biology, biochemistry, and materials science and soft condensed matter research), and

  8. Mineralogic controls on aqueous neptunium(V) concentrations in silicate systems

    International Nuclear Information System (INIS)

    The presence of radioactive neptunium in commercially spent nuclear fuel is problematic due to its mobility in environmental systems upon oxidation to the pentavalent state. As uranium is the major component of spent fuel, incorporation of neptunium into resulting U(VI) mineral phases would potentially influence its release into environmental systems. Alternatively, aqueous neptunium concentrations may be buffered by solid phase Np2O5. In this study, we investigate both of these controls on aqueous neptunium(V) concentrations. We synthesize two uranyl silicates, soddyite, (UO2)2SiO4·2H2O, and boltwoodite, (K, Na)(UO2)(SiO3OH)·1.5H2O, each in the presence of two concentrations of aqueous Np(V). Electron microscopy and electron diffraction analyses of the synthesized phases show that while significant neptunyl incorporation occurred into soddyite, the Np(V) in the boltwoodite systems largely precipitated as a secondary phase, Np2O5(s). The release of Np(V) from each system into aqueous solution was measured for several days, until steady-state concentrations were achieved. Using existing solubility constants (Ksp) for pure soddyite and boltwoodite, we compared predicted equilibrium aqueous U(VI) concentrations with the U(VI) concentrations released in the solubility experiments. Our experiments reveal that Np(V) incorporation into soddyite increases the concentration of aqueous U in equilibrium with the solid phase, perhaps via the formation of a metastable phase. In the mixed boltwoodite – Np2O5(s) system, the measured aqueous U(VI) activities are consistent with those predicted to be in equilibrium with boltwoodite under the experimental conditions, a result that is consistent with our conclusion that little Np(V) incorporation occurred into the boltwoodite. In the boltwoodite systems, the measured Np concentrations are likely controlled by the presence of Np2O5 nanoparticles, suggesting an additional potential mobility vector for Np in geologic systems. Our

  9. Monitoring corrosion and chemistry phenomena in supercritical aqueous systems

    International Nuclear Information System (INIS)

    The in situ monitoring of the chemistry and electrochemistry of aqueous heat transport fluids in thermal (nuclear and fossil) power plants is now considered essential if adequate assessment and close control of corrosion and mass transfer phenomena are to be achieved. Because of the elevated temperatures and pressures involved. new sensor technologies are required that are able to measure key parameters under plant operating conditions for extended periods of time. In this paper, the authors outline a research and development program that is designed to develop practical sensors for use in thermal power plants. The current emphasis is on sensors for measuring corrosion potential, pH, the concentrations of oxygen and hydrogen, and the electrochemical noise generated by corrosion processes at temperatures ranging from ∼250 C to 500 C. The program is currently at the laboratory stage, but testing of prototype sensors in a coal-fired supercritical power plant in Spain will begin shortly

  10. The three-component radical photoinitiating systems comprising thiacarbocyanine dye, n-butyltriphenylborate salt and N-alkoxypyridinium salt or 1,3,5-triazine derivative

    International Nuclear Information System (INIS)

    Three-component systems, which contain a light-absorbing species (thiacarbocyanine dye), an electron donor (typically n-butyltriphenylborate salt), and a third component (usually an N-alkoxypyridinium salt or 1,3,5-triazine derivative, respectively), have been applied as the efficient, visible-light-sensitive photoinitiators. The kinetic studies of free radical polymerization reveal a significant increase in polymerization rate with addition of a third component to the photoinitiating system. Although three-component systems have been consistently found to be faster and efficient than their two-component counterparts, these systems are not well understood and a number of distinct mechanisms have been reported in the literature.

  11. pH recycling aqueous two-phase systems applied in extraction of Maitake β-Glucan and mechanism analysis using low-field nuclear magnetic resonance.

    Science.gov (United States)

    Hou, Huiyun; Cao, Xuejun

    2015-07-31

    In this paper, a recycling aqueous two-phase systems (ATPS) based on two pH-response copolymers PADB and PMDM were used in purification of β-Glucan from Grifola frondosa. The main parameters, such as polymer concentration, type and concentration of salt, extraction temperature and pH, were investigated to optimize partition conditions. The results demonstrated that β-Glucan was extracted into PADB-rich phase, while impurities were extracted into PMDM-rich phase. In this 2.5% PADB/2.5% PMDM ATPS, 7.489 partition coefficient and 96.92% extraction recovery for β-Glucan were obtained in the presence of 30mmol/L KBr, at pH 8.20, 30°C. The phase-forming copolymers could be recycled by adjusting pH, with recoveries of over 96.0%. Furthermore, the partition mechanism of Maitake β-Glucan in PADB/PMDM aqueous two-phase systems was studied. Fourier transform infrared spectra, ForteBio Octet system and low-field nuclear magnetic resonance (LF-NMR) were introduced for elucidating the partition mechanism of β-Glucan. Especially, LF-NMR was firstly used in the mechanism analysis in partition of aqueous two-phase systems. The change of transverse relaxation time (T2) in ATPS could reflect the interaction between polymers and β-Glucan. PMID:26094138

  12. Extraction Equilibrium of Acrylic Acid by Aqueous Two-Phase Systems Using Hydrophilic Ionic Liquids

    International Nuclear Information System (INIS)

    As an effective method for extraction of acrylic acid, aqueous two-phase systems based on morpholinium ionic liquids were used in this study. Effects of the alkyl chain length of cation in morpholinium ionic liquids on phase diagram and extraction efficiencies were investigated. Experimental results show that aqueous two phase systems can be formed by adding appropriate amount of morpholinium ionic liquids to aqueous K2HPO4 solutions. It can be found that the ability of morpholinium ionic liquids for phase separation followed the order [HMMor][Br]>[OMMor][Br]>[BMMor][Br]>[EMMor][Br]. There was little difference between binodal curves of imidazolium ionic liquids and those of morpholinium ionic liquids. 50-90% of the extraction efficiency was observed for acrylic acid by aqueous two phase extraction of acrylic acid with morpholinium ionic liquids. It can be concluded that morpholinium ionic liquids/K2HPO4 were effective for aqueous two phases extraction of acrylic acid comparing to imidazolium ionic liquids/K2HPO4 systems because of their lower cost

  13. Complexation and extraction of halogenoacetates in ternary systems salt-water-extractant

    International Nuclear Information System (INIS)

    Consideration is given to results of investigations into uranyl halogenacetates, acetat and nitrate in ternary systems salt-water-extractant (diethyl ether or tributyl phosphate) at 25 deg C. Reciprocal solubility diagrams for uranyl salt systems are presented. Relationship between the character of phase diagram and anion properties at the fixed cation and extractant was revealed. Tendency to formation of the closed binodal curve correlates with hydration number and is connected with electron-donor ability. Deviations are explained satisfactorily by the difference in solvation numbers, which seems to be connected with steric effects. The data obtained show that relationship between anion characteristics and salt extraction ability is ambiguous. Edwards parameter should be used to obtain more accurate evaluations

  14. Gel-route treatment of waste chloride salt in A Si-P-A1 material system

    International Nuclear Information System (INIS)

    Full text: Vitrification or ceramization has been considered as one of the best choices in the immobilization of high-level radioactive wastes(HLW) as well as low- or intermediate-level wastes. However, this method requires a relatively high temperature process, which could indispensably generate secondary radioactive wastes due to the high volatility of some radionuclides. The molten salt waste released from the electochemical pyroprocess, of which function is to convert the spent oxide nuclear fuel into the metal form, consists of mainly non-active chloride salt and small amount of fission product nuclides such as Cs and Sr. Especially in Korea, the LiCl waste is expected to generate from the electrolytic reduction process. This waste raises a troublesome case in the management of radioactive wastes because of the high content of water-soluble alkali elements, high volatility and etc. In this study, our research group suggested a new method to stabilize and solidify the waste LiCl salt via a simple procedure named as a GRSS(Gel-Route Stabilization/Solidification) method. Volatility of waste was controlled by a gel-forming Si-P-Al material system in an aqueous state. The gel-forming material system consisted of sodium silicate (powder, 36wt% Na20 and 64wt% Si02, Junsei, Japan) as a gelling agent, phosphoric acid (liquid, 85% purity, Showa, Japan) as a catalyst/stabilizer and aluminum nitrate anhydrate (99% purity, Merck, Germany) as a promoter. The surrogate of the waste LiCl salt was fabricated by mixing the pure chemicals of LiCl, CsCl and SrCL '9% purity, Aldrich, Germany) with a composition of 90wt%, 6.8wt% and 3.2wt%, respectively. Two Si/P/Al ratios are used in this study (0.4/0.4/0.2 and 0.35/0.35/0.3). Each material was dissolved in deionized water and mixed together with strongly stirring for 5 min. The mixture was completely sealed and placed into an electric oven at 700C for 7 days to produce an elastic gel. The gel products were dried at 1100C for 2

  15. Salt Repository Project transportation system interface requirements: Transportation system/repository receiving facility interface requirements

    International Nuclear Information System (INIS)

    This report is a preliminary review of the interface between the transportation system and the repository receiving facility for a nuclear waste mined geologic disposal system in salt. Criteria for generic cask and facility designs are developed. These criteria are derived by examining the interfaces that occur as a result of the operations needed to receive nuclear waste at a repository. These criteria provide the basis for design of a safe, operable, practical nuclear waste receiving facility. The processing functions required to move the shipping unit from the gate into the unloading area and back to the gate for dispatch are described. Criteria for a generic receiving facility are discussed but no specific facility design is presented or evaluated. The criteria are stated in general terms to allow application to a wide variety of cask and facility designs. 9 refs., 6 figs., 4 tabs

  16. Radiation-induced reduction of metal ions in aqueous solution systems and its application

    International Nuclear Information System (INIS)

    Introduction: Promotion of chemical reactions by adding oxide particles to aqueous solution under the irradiation of ionizing radiations has been paid attention especially from the practical viewpoint, so that hydrogen production and decomposition of toxic organic compounds studied. On the other hand, redox of metal ions has not been studied very much since successive reactions after the redox become complicated due to equilibrium between reactant and product, and to transformation of dissolved species by varying pH and coexisting ions... In the present study, reduction behavior of metal ions in aqueous solution systems irradiated by r-ray and electron beam was measured, the reduced amount was compared with that by water radiolysis, and then the promotion of reduction by adding oxide particles was found out quantitatively. Experimental: Samples were prepared by dissolving metal salts (Ce(IV), Cr(VI), Pt(IV),...) in 0.4 mol/L sulfuric acid or 0.1 mol/l sodium perchlorate solution and then by adding 1-10 wt% oxide particles such as TiO2, Al2O3 or SiO2 to the solution. The irradiation of sample was made without stirring the particles in the solution mainly by using 60Co γ-ray source (dose rate: 1-30 kGy/h) at Takasaki Research Institute, JAEA; the absorbed dose of sample was estimated by using dosimeters of dichromate solution and/or CTA film. Just after irradiated, the sample was passed through a membrane filter to be separated into solution and solid components; absorption spectrum of metal ions in the solution was observed, and the reduced amount determined from difference in the absorbance before and after the irradiation. Results and discussion: Figure 1 shows absorption spectra of Ce(IV) ion in 0.4 mol/L H2SO4 solution under the γ-ray irradiation as typical results. Fig.1(a) illustrates that the reduction was observed in the solution without the oxide particles as stoichiometry in the one-electron reduction by water radiolysis has been used as a dosimeter, and

  17. Alternative (Potentially Green) Separations Media: Aqueous Biphasic and Related Systems Extending the Frontier Final Report For Period September 1, 2002 January 31, 2007

    Energy Technology Data Exchange (ETDEWEB)

    Rogers, Robin D

    2007-06-25

    Through the current DoE-BES funding, we have extended our fundamental understanding of the critical phase separation of aqueous polymer solutions at the molecular level, and have developed a similar understanding of their application as novel solvent systems. Our principal aims included mode of delivery of the aqueous biphasic system (ABS) solvent system and the application of this system to problems of reactive extraction. In the former case we have developed novel solid phase analogues, in the form of cross-linked polyethylene glycol hydrogels, and in the latter case we have examined the role that ABS might play in reaction engineering, with a view to greener, simpler, and safer processes. We have also developed a new salt/salt ABS and have extended our understanding of this system as well. The major outcomes are as follows: (1) Through the use of variable temperature phase diagrams, coupled with differential scanning calorimetry (DSC) measurements of the phases, a better understanding of the thermodynamics of phase formation was obtained. Evidence to the existence and role of an upper critical solution temperature (UCST) or lower critical solution temperature (LCST) (or both) in these systems was gained. With variable temperature solute partitioning, thermodynamic parameters were calculated, and inter-system comparisons were made. Through the use of Abraham's linear solvation energy regression (LSER) the solvent-solute properties of liquid/liquid ABS were examined. We have shown that ABS are indeed very tunable and LSERs have been used as a tool to compare these systems to traditional organic/water and other liquid/liquid systems. (2) We have successfully shown the development of novel reaction media for chemical synthesis and reaction; Aqueous Biphasic Reactive Extraction (ABRE). As a proof of concept, we have shown the synthesis of adipic acid from cyclohexene in an ABS, which represents an important development in the exploitation of this technology

  18. Salt cookbook

    CERN Document Server

    Saha, Anirban

    2015-01-01

    If you are a professional associated with system and infrastructure management, looking at automated infrastructure and deployments, then this book is for you. No prior experience of Salt is required.

  19. Materials considerations for molten salt accelerator-based plutonium conversion systems

    International Nuclear Information System (INIS)

    Accelerator-driven transmutation technology (ADTT) refers to a concept for a system that uses a blanket assembly driven by a source of neutrons produced when high-energy protons from an accelerator strike a heavy metal target. One application for such a system is called Accelerator-Based Plutonium Conversion, or ABC. Currently, the version of this concept being proposed by the Los Alamos National Laboratory features a liquid lead target material and a blanket fuel of molten fluorides that contain plutonium. Thus, the materials to be used in such a system must have, in addition to adequate mechanical strength, corrosion resistance to molten lead, corrosion resistance to molten fluoride salts, and resistance to radiation damage. In this report the corrosion properties of liquid lead and the LiF-BeF2 molten salt system are reviewed in the context of candidate materials for the above application. Background information has been drawn from extensive past studies. The system operating temperature, type of protective environment, and oxidation potential of the salt are shown to be critical design considerations. Factors such as the generation of fission products and transmutation of salt components also significantly affect corrosion behavior, and procedures for inhibiting their effects are discussed. In view of the potential for extreme conditions relative to neutron fluxes and energies that can occur in an ADTT, a knowledge of radiation effects is a most important factor. Present information for potential materials selections is summarized

  20. Natural gas hydrate formation and inhibition in gas/crude oil/aqueous systems

    DEFF Research Database (Denmark)

    Daraboina, Nagu; Pachitsas, Stylianos; von Solms, Nicolas

    2015-01-01

    Gas hydrate formation in multi phase mixtures containing an aqueous phase (with dissolved salts), reservoir fluid (crude oil) and natural gas phase was investigated by using a standard rocking cell (RC-5) apparatus. The hydrate formation temperature was reduced in the presence of crude oils...... in comparison with that in pure water. This observed hydrate inhibition potential shows significant variation depending on the type of crude oil. The influence of crude oil composition (saturates, aromatics, resins and asphaltenes) on this behavior was probably due to the existence of a combination of different...... inhibition mechanisms and potentially a competition among inhibition-promotion mechanisms. Moreover, the hydrate formation time has been determined at different water cuts in each crude oil and it was found that the inhibition capability increases with an increase in the oil content. The effect...

  1. Nuclear performance of molten salt fusion--fission symbiotic systems for catalyzed DD and DT reactors

    International Nuclear Information System (INIS)

    The nuclear performance of a fusion-fission hybrid reactor having a molten salt composed of Na-Th-F-Be as the blanket fertile material and operating with a catalyzed DD plasma is compared to a similar system utilizing a Li-Th-F-Be salt and operating with a DT plasma. The production of fissile fuel via the 232Th-233U fuel cycle was considered on the basis of its potential nonproliferation aspects. The calculations were performed using one-dimensional discrete ordinates methods to compare neutron balances, fuel producion rates, energy deposition rates, and the radiation damage in the reactor structure

  2. An experimental test plan for the characterization of molten salt thermochemical properties in heat transport systems

    Energy Technology Data Exchange (ETDEWEB)

    Pattrick Calderoni

    2010-09-01

    Molten salts are considered within the Very High Temperature Reactor program as heat transfer media because of their intrinsically favorable thermo-physical properties at temperatures starting from 300 C and extending up to 1200 C. In this context two main applications of molten salt are considered, both involving fluoride-based materials: as primary coolants for a heterogeneous fuel reactor core and as secondary heat transport medium to a helium power cycle for electricity generation or other processing plants, such as hydrogen production. The reference design concept here considered is the Advanced High Temperature Reactor (AHTR), which is a large passively safe reactor that uses solid graphite-matrix coated-particle fuel (similar to that used in gas-cooled reactors) and a molten salt primary and secondary coolant with peak temperatures between 700 and 1000 C, depending upon the application. However, the considerations included in this report apply to any high temperature system employing fluoride salts as heat transfer fluid, including intermediate heat exchangers for gas-cooled reactor concepts and homogenous molten salt concepts, and extending also to fast reactors, accelerator-driven systems and fusion energy systems. The purpose of this report is to identify the technical issues related to the thermo-physical and thermo-chemical properties of the molten salts that would require experimental characterization in order to proceed with a credible design of heat transfer systems and their subsequent safety evaluation and licensing. In particular, the report outlines an experimental R&D test plan that would have to be incorporated as part of the design and operation of an engineering scaled facility aimed at validating molten salt heat transfer components, such as Intermediate Heat Exchangers. This report builds on a previous review of thermo-physical properties and thermo-chemical characteristics of candidate molten salt coolants that was generated as part of the

  3. Salt Water Intrusion in a Three-dimensional Groundwater System in The Netherlands: a Numerical Study

    NARCIS (Netherlands)

    Oude Essink, Gualbert

    2001-01-01

    Salt water intrusion is investigated in a coastal groundwater system in the northern part of the province Noord-Holland, The Netherlands. Density dependent groundwater flow is modeled in three-dimensions withMOCDENS3D. This computer code is a version of MOC3D (Konikow et al., 1996) that has been ada

  4. A Novel Modeling of Molten-Salt Heat Storage Systems in Thermal Solar Power Plants

    Directory of Open Access Journals (Sweden)

    Rogelio Peón Menéndez

    2014-10-01

    Full Text Available Many thermal solar power plants use thermal oil as heat transfer fluid, and molten salts as thermal energy storage. Oil absorbs energy from sun light, and transfers it to a water-steam cycle across heat exchangers, to be converted into electric energy by means of a turbogenerator, or to be stored in a thermal energy storage system so that it can be later transferred to the water-steam cycle. The complexity of these thermal solar plants is rather high, as they combine traditional engineering used in power stations (water-steam cycle or petrochemical (oil piping, with the new solar (parabolic trough collector and heat storage (molten salts technologies. With the engineering of these plants being relatively new, regulation of the thermal energy storage system is currently achieved in manual or semiautomatic ways, controlling its variables with proportional-integral-derivative (PID regulators. This makes the overall performance of these plants non optimal. This work focuses on energy storage systems based on molten salt, and defines a complete model of the process. By defining such a model, the ground for future research into optimal control methods will be established. The accuracy of the model will be determined by comparing the results it provides and those measured in the molten-salt heat storage system of an actual power plant.

  5. Nuclear power technology system with molten salt reactor for transuranium nuclides burning in closed fuel cycle

    International Nuclear Information System (INIS)

    A concept of nuclear power technology system with homogeneous molten salt reactors for burning and transmutation of long-lived radioactive toxic nuclides is considered in the paper. Disposition of such reactors in enterprises of fuel cycle allows to provide them with power and facilitate solution of problems with rad waste with minimal losses. (Authors)

  6. Ventilation system consequence calculations to support salt well pumping single-shell tank 241-A-101

    International Nuclear Information System (INIS)

    This document presents the radiological dose and toxicological exposure calculations for an accident scenario involved with the ventilation system used to support salt well pumping single-shell tank 241-A-101. This tank has been listed on the Hydrogen Watch List

  7. Multi-functional sensor system for molten salt technologies

    Science.gov (United States)

    Redey, Laszlo; Gourishankar, Karthick; Williamson, Mark A.

    2009-12-15

    The present invention relates to a multi-functional sensor system that simultaneously measures cathode and anode electrode potentials, dissolved ion (i.e. oxide) concentration, and temperatures in an electrochemical cell. One embodiment of the invented system generally comprises: a reference(saturated) electrode, a reference(sensing) electrode, and a data acquisition system. Thermocouples are built into the two reference electrodes to provide important temperature information.

  8. Reductive extraction of radionuclides in molten salt/liquid metal systems

    International Nuclear Information System (INIS)

    The extraction behavior of several lanthanide and actinide elements in the reductive-oxidative extraction systems of LiF-BeF2/Bi and LiCl-LiF/Bi is described. The equilibrium distributions of the elements are affected by metal composition as well as salt composition. The observed effects support the formation of complex compounds in the salt phase and of intermetallic compounds in the metal phase. The equilibrium distributions are discussed on the basis of thermodynamics. From the practical technological point of view, the extraction rate of the elements from the salt phase to the metal phase is also discussed by considering mass transfers at the interface between the two phases. (author)

  9. Solubility in aqueous system of potassium sulfate, cadmium sulfate at 50 deg C

    International Nuclear Information System (INIS)

    Solubility in system potassium sulfate-cadmium sulfate-water at 50 deg C is studied using isothermal method. Crystallization limits of K2SO4, CdSO4x8/3H2O double salt 2K2SO4x2CdSO4x3H2O at 50 deg C are determined

  10. Seismic characterization of the Wasatch fault system beneath Salt Lake City using a land streamer system

    Science.gov (United States)

    Brophy, B.; Liberty, L. M.; Gribler, G.

    2015-12-01

    We characterize the active Wasatch fault system beneath downtown Salt Lake City by measuring p- and s-wave velocities and seismic reflection profiling. Our focus was on the segment boundary between the Warm Springs and East Bench faults. We collected 14.5 km along 9 west-east profiles in 3 field days using a 60 m aperture seismic land streamer and 200 kg weight drop system. From a p-wave refraction analysis, we measure velocities from 230-3900 m/s for the upper 20-25 meters. Shear wave velocities for the upper 30 m, derived from a multi-channel analysis of surface waves (MASW) approach, show velocities that range from 100-1800 m/s. P-wave reflection images from the upper 100 m depth indicate offset and truncated (mostly) west-dipping strata (Bonneville Lake deposits?) that suggest active faults extend beneath the downtown urban corridor. We identify saturated sediments on the lower elevation (western) portions of the profiles and shallow high velocity (dry) strata to the east of the mapped faults. We observe slow p-wave velocities near identified faults that may represent the fault's colluvial wedge. These velocity results are best highlighted with Vp/Vs ratios. Analyzing shear wave velocities by NEHRP class, we estimate soft soil (NEHRP D) limited less than 1 m depth along most profiles, and stiff soil (NEHRP C) to up to 25 m depth in some locations. However near steep topographic slopes (footwall deposits), we identify NEHRP Class D stiff soil velocities to less than 2 m depth before transition to NEHRP Class C soft rock. Depth to hard rock (velocities >760 m/s) are as shallow as 20 m below the land surface on some steep slopes beneath north Salt Lake City and greater than our imaging depths along the western portions of our profiles. Our findings suggest large variations in seismic velocities beneath the Salt Lake City corridor and that multiple fault strands related to the Warm Springs fault segment extend beneath downtown.

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

    International Nuclear Information System (INIS)

    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 1H nuclear magnetic resonance (1H 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

  12. 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

  13. Geomorphic and Aqueous Chemistry of a Portion of the Upper Rio Tinto System, Spain

    Science.gov (United States)

    Osburn, M. R.; Fernandez-Remolar, D. C.; Arvidson, R. E.; Morris, R. V.; Ming, D.; Prieto-Ballesteros, O.; Amils, R.; Stein, T. C.; Heil-Chapdelaine, V.; Friedlander, L. R.; Herndon, B.; Marlow, J.; Rosenberg, S.; Scherpker, K.; Steiner, A.

    2007-01-01

    Observations from the two Mars rovers, Spirit and Opportunity, combined with discoveries of extensive hydrated sulfate deposits from OMEGA and CRISM show that aqueous deposition and alteration involving acidic systems and sulfate deposition has been a key contributor to the martian geologic record. Rio Tinto, Spain, provides a process model for formation of sulfates on Mars by evaporation of acidic waters within shallow fluvial pools, particularly during dry seasons. We present results from a detailed investigation of an upper portion of the Rio Tinto, focusing on geomorphology, clastic sediment transport, and acidic aqueous processes. We also lay out lessons-learned for under-standing sulfate formation and alteration on Mars.

  14. Customer interface document for the Molten Salt Test Loop (MSTL) system.

    Energy Technology Data Exchange (ETDEWEB)

    Pettit, Kathleen; Kolb, William J.; Gill, David Dennis; Briggs, Ronald D.

    2012-03-01

    The National Solar Thermal Test Facility at Sandia National Laboratories has a unique test capability called the Molten Salt Test Loop (MSTL) system. MSTL is a test capability that allows customers and researchers to test components in flowing, molten nitrate salt. The components tested can range from materials samples, to individual components such as flex hoses, ball joints, and valves, up to full solar collecting systems such as central receiver panels, parabolic troughs, or linear Fresnel systems. MSTL provides realistic conditions similar to a portion of a concentrating solar power facility. The facility currently uses 60/40 nitrate 'solar salt' and can circulate the salt at pressure up to 600psi, temperature to 585 C, and flow rate of 400-600GPM depending on temperature. The purpose of this document is to provide a basis for customers to evaluate the applicability to their testing needs, and to provide an outline of expectations for conducting testing on MSTL. The document can serve as the basis for testing agreements including Work for Others (WFO) and Cooperative Research and Development Agreements (CRADA). While this document provides the basis for these agreements and describes some of the requirements for testing using MSTL and on the site at Sandia, the document is not sufficient by itself as a test agreement. The document, however, does provide customers with a uniform set of information to begin the test planning process.

  15. Molten Salt-Carbon Nanotube Thermal Energy Storage for Concentrating Solar Power Systems Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Michael Schuller; Frank Little; Darren Malik; Matt Betts; Qian Shao; Jun Luo; Wan Zhong; Sandhya Shankar; Ashwin Padmanaban

    2012-03-30

    We demonstrated that adding nanoparticles to a molten salt would increase its utility as a thermal energy storage medium for a concentrating solar power system. Specifically, we demonstrated that we could increase the specific heat of nitrate and carbonate salts containing 1% or less of alumina nanoparticles. We fabricated the composite materials using both evaporative and air drying methods. We tested several thermophysical properties of the composite materials, including the specific heat, thermal conductivity, latent heat, and melting point. We also assessed the stability of the composite material with repeated thermal cycling and the effects of adding the nanoparticles on the corrosion of stainless steel by the composite salt. Our results indicate that stable, repeatable 25-50% improvements in specific heat are possible for these materials. We found that using these composite salts as the thermal energy storage material for a concentrating solar thermal power system can reduce the levelized cost of electricity by 10-20%. We conclude that these materials are worth further development and inclusion in future concentrating solar power systems.

  16. Purification of C-phycocyanin from Spirulina platensis in aqueous two-phase systems using an experimental design

    Directory of Open Access Journals (Sweden)

    Francine Silva Antelo

    2015-02-01

    Full Text Available C-phycocyanin from Spirulina platensis was purified in aqueous two-phase systems (ATPS of polyethylene glycol (PEG/potassium phosphate, varying the molar mass of the PEG. Results using a full factorial design showed that an increase in the concentration of salt and decrease in the concentration of PEG caused an increment in the purification factor for all the ATPS studied. Optimization of the conditions of the purification was studied using a central composite rotatable design for each molar mass of PEG. The ATPS composed of 7% (w/w PEG 1500 or 4% (w/w PEG 8000 (g/gmol and 23 or 22.5% (w/w of phosphate resulted a purification factor of 1.6-fold for C-phycocyanin, with total and 57% recovery, respectively. Process conditions were optimized for the purification factor for the system with PEG 1500. The ATPS with 4% (w/w PEG 4000 or 4% (w/w PEG 6000 and 21% (w/w phosphate resulted purification factors of 2.1 and 2.2-fold, recovering 100% and 73.5%, respectively of C-phycocyanin in the top phase.

  17. Surface tension and related thermodynamic quantities of aqueous electrolyte solutions

    CERN Document Server

    Matubayasi, Norihiro

    2013-01-01

    Surface tension provides a thermodynamic avenue for analyzing systems in equilibrium and formulating phenomenological explanations for the behavior of constituent molecules in the surface region. While there are extensive experimental observations and established ideas regarding desorption of ions from the surfaces of aqueous salt solutions, a more successful discussion of the theory has recently emerged, which allows the quantitative calculation of the distribution of ions in the surface region. Surface Tension and Related Thermodynamic Quantities of Aqueous Electrolyte Solutions provides a d

  18. Salt-free vesicle-phases and their template effect

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Researches on the construction, structure, and formation of vesicles formed from surfactants have attracted great attention from colloid and interface chemists. The vesicles formed from salt-free cationic-anionic surfactant systems are very different from those with excess salts, having many particular properties. In this paper, we introduce the properties of vesicles prepared from salt-free surfactant systems, according to our own results, especially the vesicles formed from surfactants with divalent metal ions as counterions in aqueous solutions and room temperature ionic liquids. Moreover, the primary results on template effect of the metal-ligand vesicles have also been summarized.

  19. High-temperature molten salt thermal energy storage systems for solar applications

    Science.gov (United States)

    Petri, R. J.; Claar, T. D.; Ong, E.

    1983-01-01

    Experimental results of compatibility screening studies of 100 salt/containment/thermal conductivity enhancement (TCE) combinations for the high temperature solar thermal application range of 704 deg to 871 C (1300 to 1600 F) are presented. Nine candidate containment/HX alloy materials and two TCE materials were tested with six candidate solar thermal alkali and alkaline earth carbonate storage salts (both reagent and technical grade of each). Compatibility tests were conducted with salt encapsulated in approx. 6.0 inch x 1 inch welded containers of test material from 300 to 3000 hours. Compatibility evaluations were end application oriented, considering the potential 30 year lifetime requirement of solar thermal power plant components. Analyses were based on depth and nature of salt side corrosion of materials, containment alloy thermal aging effects, weld integrity in salt environment, air side containment oxidation, and chemical and physical analyses of the salt. A need for more reliable, and in some cases first time determined thermophysical and transport property data was also identified for molten carbonates in the 704 to 871 C temperature range. In particular, accurate melting point (mp) measurements were performed for Li2CO3 and Na2CO3 while melting point, heat of fusion, and specific heat determinations were conducted on 81.3 weight percent Na2CO3-18.7 weight percent K2CO3 and 52.2 weight percent BaCO3-47.8 weight percent Na2CO3 to support future TES system design and ultimate scale up of solar thermal energy storage (TES) subsystems.

  20. Separation of aqueous two-phase polymer systems in microgravity

    Science.gov (United States)

    Vanalstine, J. M.; Harris, J. M.; Synder, S.; Curreri, P. A.; Bamberger, S. B.; Brooks, D. E.

    1984-01-01

    Phase separation of polymer systems in microgravity is studied in aircraft flights to prepare shuttle experiments. Short duration (20 sec) experiments demonstrate that phase separation proceeds rapidly in low gravity despite appreciable phase viscosities and low liquid interfacial tensions (i.e., 50 cP, 10 micro N/m). Ostwald ripening does not appear to be a satisfactory model for the phase separation mechanism. Polymer coated surfaces are evaluated as a means to localize phases separated in low gravity. Contact angle measurements demonstrate that covalently coupling dextran or PEG to glass drastically alters the 1-g wall wetting behavior of the phases in dextran-PEG two phase systems.

  1. Thorium Molten-Salt Nuclear Energy Synergetics system for the global energy demand

    International Nuclear Information System (INIS)

    In this century, we have to solve the two antithetical energy problems. The one is a huge and steep energy demand by the population explosion and the other is a CO2 emission reduction for preventing global warming. It is clear that innovative nuclear system satisfying the following conditions can only solve these problems: adequate safety; nuclear proliferation resistance and safeguards; economic competitiveness; improved radio-waste management; resource utilization, and flexible applicability. To meet these conditions, a new concept THORIMS-NES (Thorium Molten-Salt Nuclear Energy Synergetics) has been proposed, which is composed of simple molten-salt reactors (FUJI) and Accelerator Molten-Salt Breeders (AMSB) which produce the fissile 233U from Th and feed it to the nearly self-sustaining molten-salt reactor FUJI. A number of FUJIs can use 239Pu as part of their fissile fuel along with the fertile Th thereby eliminating the excess Pu in the world. A nuclear option for Brazil using this system is presented. (author)

  2. Replacing bare fallow with cover crops in an irrigated cropping system: soil salinity and salt leaching

    OpenAIRE

    Almendros García, Patricia; Gabriel Pérez, José Luis; Quemada Saenz-Badillos, Miguel

    2011-01-01

    In irrigated areas where cover crop establishment can be assured, consequent soil or nutrient conservation could increase sustainability of cropping systems. Replacing bare fallow with cover crops may increase sustainability by enhancing soil aggregate stability, water retention capacity or controlling nitrate leaching. Nevertheless, adoption of cover crops increase evapotranspiration and reduce water percolation beyond the root systems; therefore, it could lead to salt accumulation in the up...

  3. Direct Observation of Formation Behavior of Metal Emulsion in Sn/Salt System

    Science.gov (United States)

    Yoshida, Hironori; Liu, Jiang; Kim, Sun-Joong; Gao, Xu; Ueda, Shigeru; Maruoka, Nobuhiro; Ono, Shinpei; Kitamura, Shin-ya

    2016-08-01

    Using two systems with different interfacial tensions, the behavior of metal emulsions during bottom blowing was observed directly with a high-speed camera. The interfacial tension between molten salt (KCl-LiCl-NaCl) and molten Sn was measured by a pendant drop method, and it decreased to about 100 mN/m when the Te content in Sn increased from 0 to 0.5 pct. In both systems, two types of metal emulsion behaviors were observed. In Mode A, fine metal droplets were formed after the metal film ruptured at the interface. In Mode B, the formation of coarse droplets was observed after the disintegration of the column generated by the rising bubble, and the number of droplets increased with the gas flow rate compared to that in Mode A. The generating frequency of each mode revealed that Mode B became dominant with increasing gas flow rate. In the pure Sn/salt system, the numbers of droplets of Mode B showed a local maximum at high gas flow rates, but the numbers of droplets in Sn-0.5 pctTe/salt increased continuously even in the same flow range. Regarding the size distribution, the percentage of coarse metal droplets in the Sn-0.5 pctTe alloy/salt was larger than that in the pure Sn/salt. Furthermore, the effect of interfacial tension on the variation in surface area and volume of the droplets showed a similar tendency for the column height. Therefore, a decrement of the interfacial tension led to an increment of the column height when Mode B occurred and finally resulted in a higher interfacial area.

  4. Direct Observation of Formation Behavior of Metal Emulsion in Sn/Salt System

    Science.gov (United States)

    Yoshida, Hironori; Liu, Jiang; Kim, Sun-Joong; Gao, Xu; Ueda, Shigeru; Maruoka, Nobuhiro; Ono, Shinpei; Kitamura, Shin-ya

    2016-05-01

    Using two systems with different interfacial tensions, the behavior of metal emulsions during bottom blowing was observed directly with a high-speed camera. The interfacial tension between molten salt (KCl-LiCl-NaCl) and molten Sn was measured by a pendant drop method, and it decreased to about 100 mN/m when the Te content in Sn increased from 0 to 0.5 pct. In both systems, two types of metal emulsion behaviors were observed. In Mode A, fine metal droplets were formed after the metal film ruptured at the interface. In Mode B, the formation of coarse droplets was observed after the disintegration of the column generated by the rising bubble, and the number of droplets increased with the gas flow rate compared to that in Mode A. The generating frequency of each mode revealed that Mode B became dominant with increasing gas flow rate. In the pure Sn/salt system, the numbers of droplets of Mode B showed a local maximum at high gas flow rates, but the numbers of droplets in Sn-0.5 pctTe/salt increased continuously even in the same flow range. Regarding the size distribution, the percentage of coarse metal droplets in the Sn-0.5 pctTe alloy/salt was larger than that in the pure Sn/salt. Furthermore, the effect of interfacial tension on the variation in surface area and volume of the droplets showed a similar tendency for the column height. Therefore, a decrement of the interfacial tension led to an increment of the column height when Mode B occurred and finally resulted in a higher interfacial area.

  5. Determining salt concentrations for equivalent water activity in reduced-sodium cheese by use of a model system.

    Science.gov (United States)

    Grummer, J; Schoenfuss, T C

    2011-09-01

    The range of sodium chloride (salt)-to-moisture ratio is critical in producing high-quality cheese products. The salt-to-moisture ratio has numerous effects on cheese quality, including controlling water activity (a(w)). Therefore, when attempting to decrease the sodium content of natural cheese it is important to calculate the amount of replacement salts necessary to create the same a(w) as the full-sodium target (when using the same cheese making procedure). Most attempts to decrease sodium using replacement salts have used concentrations too low to create the equivalent a(w) due to the differences in the molecular weight of the replacers compared with salt. This could be because of the desire to minimize off-flavors inherent in the replacement salts, but it complicates the ability to conclude that the replacement salts are the cause of off-flavors such as bitter. The objective of this study was to develop a model system that could be used to measure a(w) directly, without manufacturing cheese, to allow cheese makers to determine the salt and salt replacer concentrations needed to achieve the equivalent a(w) for their existing full-sodium control formulas. All-purpose flour, salt, and salt replacers (potassium chloride, modified potassium chloride, magnesium chloride, and calcium chloride) were blended with butter and water at concentrations that approximated the solids, fat, and moisture contents of typical Cheddar cheese. Salt and salt replacers were applied to the model systems at concentrations predicted by Raoult's law. The a(w) of the model samples was measured on a water activity meter, and concentrations were adjusted using Raoult's law if they differed from those of the full-sodium model. Based on the results determined using the model system, stirred-curd pilot-scale batches of reduced- and full-sodium Cheddar cheese were manufactured in duplicate. Water activity, pH, and gross composition were measured and evaluated statistically by linear mixed model

  6. Ion mixing, hydration, and transport in aqueous ionic systems

    International Nuclear Information System (INIS)

    The enhancement effect on the ion mobility of fluoride (and that of chloride) in a polycationic system, as the chloride content increases, is shown to also exist in other more simple ionic systems with cations such as the cesium ion and an organic ammonium ion. As the chloride content increases, in addition to the finding that there is more unbound water associated with the cation, we also observe that the average lifetime of a hydrogen bond decreases. This change to the hydrogen bonds is correlated to significant changes to both the structural and dynamical properties of water. The more disordered water structure and faster water dynamics are hypothesized to be also responsible for the enhanced ion mobilities. Furthermore, when either the chloride content or hydration level is changed, the self-diffusion constant of each co-ion changes by almost the same factor, implying the existence of a single universal transport mechanism that determines ion mobilities

  7. Development of ketoprofen delivery systems based on aqueous polyurethane dispersions

    OpenAIRE

    Leite, E; Fernandes, I; Ayres, E.; Barreiro, M.F.; Silva-Cunha, A.

    2013-01-01

    Ketoprofen (2-(3-benzoylphenyl) propionic acid) is a non-steroidal anti-inflammatory drug (NSAID) used to treat a wide range of acute and chronic inflammatory diseases, e.g., rheumatoid arthritis, osteoarthritis and ankylosing spondylitis. Its prolonged oral administration is associated with several gastrointestinal reactions such as irritation and ulceration. In this context, ketoprofen is a good candidate for controlled release administration systems. This work aims to test the suitabili...

  8. Binary Nucleation in Aqueous Electrolyte Systems. Sodium Chloride

    Czech Academy of Sciences Publication Activity Database

    Němec, Tomáš; Maršík, František

    Gdansk: IFFM Publishers, 2005 - (Mikielewicz, J.; Butrymowicz, D.; Trela, M.; Cieslinski, J.), s. 395-400 ISBN 83-88237-90-X. [HEAT 2005 : International Conference on Transport Phenomena in Multiphase Systems. Gdansk (PL), 26.06.2005-30.06.2005] R&D Projects: GA ČR(CZ) GA101/05/2536 Institutional research plan: CEZ:AV0Z20760514 Keywords : binary nucleation * sodium chloride * water Subject RIV: BJ - Thermodynamics

  9. Dissolution state of cellulose in aqueous systems. 2. Acidic solvents.

    Science.gov (United States)

    Alves, Luis; Medronho, Bruno; Antunes, Filipe E; Topgaard, Daniel; Lindman, Björn

    2016-10-20

    Cellulose is insoluble in water but can be dissolved in strong acidic or alkaline conditions. How well dissolved cellulose is in solution and how it organizes are key questions often neglected in literature. The typical low pH required for dissolving cellulose in acidic solvents limits the use of typical characterization techniques. In this respect, Polarization Transfer Solid State NMR (PT ssNMR) emerges as a reliable alternative. In this work, combining PT ssNMR, microscopic techniques and X-ray diffraction, a set of different acidic systems (phosphoric acid/water, sulfuric acid/glycerol and zinc chloride/water) is investigated. The studied solvent systems are capable to efficiently dissolve cellulose, although degradation occurs to some extent. PT ssNMR is capable to identify the liquid and solid fractions of cellulose, the degradation products and it is also sensitive to gelation. The materials regenerated from the acidic dopes were found to be highly sensitive to the solvent system and to the presence of amphiphilic additives in solution. PMID:27474617

  10. Ion Dynamics Study of Potato Starch + Sodium Salts Electrolyte System

    Directory of Open Access Journals (Sweden)

    Tuhina Tiwari

    2013-01-01

    Full Text Available The effect of different anions, namely, SCN−, I−, and ClO4−, on the electrical properties of starch-based polymer electrolytes has been studied. Anion size and conductivity are having an inverse trend indicating systems to be predominantly anionic conductor. Impact of anion size and multiplet forming tendency is reflected in number of charge carriers and mobility, respectively. Ion dynamics study reveals the presence of different mechanisms in different frequency ranges. Interestingly, superlinear power law (SLPL is found to be present at <5 MHz frequency, which is further confirmed by dielectric data.

  11. Rapid RNA Exchange in Aqueous Two-Phase System and Coacervate Droplets

    OpenAIRE

    Jia, Tony Z.; Hentrich, Christian; SZOSTAK, JACK W.

    2014-01-01

    Compartmentalization in a prebiotic setting is an important aspect of early cell formation and is crucial for the development of an artificial protocell system that effectively couples genotype and phenotype. Aqueous two-phase systems (ATPSs) and complex coacervates are phase separation phenomena that lead to the selective partitioning of biomolecules and have recently been proposed as membrane-free protocell models. We show in this study through fluorescence recovery after photobleaching (FR...

  12. Use of metal complexation in non-aqueous capillary electrophoresis systems for the separation and improved detection of tetracyclines.

    Science.gov (United States)

    Tjørnelund, J; Hansen, S H

    1997-08-29

    Metal complexation in non-aqueous capillary electrophoresis systems was evaluated for the separation and improved detection of tetracycline antibiotics using laser-induced fluorescence detection. It was found that three factors were important for the choice of complexing agent: (i) it should be soluble in the organic solvent used for the separation, (ii) it should have a sufficient fast complexing rate so as not to invalidate the electrophoretic separation and, (iii) it should give a large increase in the fluorescence intensity. Mg2+ ions were found to be the most suitable ions for the separation of the tetracyclines as the acetate salt of magnesium is very soluble in organic solvents and only a relatively low current was generated during electrophoresis making it possible to use high concentrations of the complexing metal ion. Metal complexation strongly intensified the fluorescence of tetracyclines and all organic solvents investigated further intensified the fluorescence, e.g. dimethylformamide improved the fluorescence of the oxytetracycline metal complex by a factor of 34 compared to water. However, magnesium acetate was not sufficiently soluble in dimethylformamide and therefore N-methylformamide, improving the fluorescence intensity by only a factor of 9, was used. It was demonstrated that the method can be used for the detection of tetracyclines at the ppb level in milk and plasma. PMID:9335125

  13. Development of green betaine-based deep eutectic solvent aqueous two-phase system for the extraction of protein.

    Science.gov (United States)

    Li, Na; Wang, Yuzhi; Xu, Kaijia; Huang, Yanhua; Wen, Qian; Ding, Xueqin

    2016-05-15

    Six kinds of new type of green betaine-based deep eutectic solvents (DESs) have been synthesized. Deep eutectic solvent aqueous two-phase systems (DES-ATPS) were established and successfully applied in the extraction of protein. Betaine-urea (Be-U) was selected as the suitable extractant. Single factor experiments were carried out to determine the optimum conditions of the extraction process, such as the salt concentration, the mass of DES, the separation time, the amount of protein, the temperature and the pH value. The extraction efficiency could achieve to 99.82% under the optimum conditions. Mixed sample and practical sample analysis were discussed. The back extraction experiment was implemented and the back extraction efficiency could reach to 32.66%. The precision experiment, repeatability experiment and stability experiment were investigated. UV-vis, FT-IR and circular dichroism (CD) spectra confirmed that the conformation of protein was not changed during the process of extraction. The mechanisms of extraction were researched by dynamic light scattering (DLS), the measurement of the conductivity and transmission electron microscopy (TEM). DES-protein aggregates and embraces phenomenon play considerable roles in the separation process. All of these results indicated that betaine-based DES-ATPS may provide a potential substitute new method for the separation of proteins. PMID:26992491

  14. Structure and dynamics of a salt-bridge model system in water and DMSO

    Science.gov (United States)

    Lotze, S.; Bakker, H. J.

    2015-06-01

    We study the interaction between the ions methylguanidinium and trifluoroacetate dissolved in D2O and dimethylsulfoxide with linear infrared spectroscopy and femtosecond two-dimensional infrared spectroscopy. These ions constitute model systems for the side chains of arginine and glutamic and aspartic acid that are known to form salt bridges in proteins. We find that the salt-bridge formation of methylguanidinium and trifluoroacetate leads to a significant acceleration of the vibrational relaxation dynamics of the antisymmetric COO stretching vibration of the carboxyl moiety of trifluoroacetate. Salt-bridge formation has little effect on the rate of the spectral fluctuations of the CN stretching vibrations of methylguanidinium. The anisotropy of the cross peaks between the antisymmetric COO stretching vibration of trifluoroacetate and the CN stretching vibrations of methylguanidinium reveals that the salt-bridge is preferentially formed in a bidentate end-on configuration in which the two C=O groups of the carboxylate moiety form strong hydrogen bonds with the two -NH2 groups of methylguanidinium.

  15. Nitrogen electrode reaction and its applications in molten salts system

    Energy Technology Data Exchange (ETDEWEB)

    Itoh, Yasuhiko; Gotoh, Takuya [Kyoto Univ. (Japan)

    2001-12-01

    Electrical behaviors of nitrogen gas electrode and its compounds are studied in the molten LiCl-KCl system. Nitrogen gas was found to be reduced to nitride ion (N{sup 3-}) by the 3-electron reaction (standard mono electrode potential: 0.382 V vs. Li{sup +}/Li, 723 K) of 1/2N{sub 2} + 3e=N{sup 3-}. It was found that the gas electrode with porous Ni was excellent in the study of the relation between the polarization characteristics and the electrode material. On the thermodynamic possibility of new process participating in nitrogen the E-pN{sup 3-} diagram was drawn to discuss the relation of ion concentration of N{sup 3-} and partial pressure N{sub 2} gas in accordance with the standard mono electrode potential of N{sub 2}/N{sup 3-} and with thermodynamic data of nitrides. On basis of these analysis the new engineering processes, such as dry reprocessing, were found to be able to propose to the spend nitride fuel and to the electrolysis synthesis of ammonium. (H. Katsuta)

  16. Critical issues in the use of metals and alloys in sulphur-containing aqueous systems

    Energy Technology Data Exchange (ETDEWEB)

    Macdonald, D.D.

    1992-12-31

    Sulphur-containing aqueous fluids are amongst the most corrosive environments experienced in industrial and natural systems. The high corrosivity is due principally to the wide range of oxidation states that sulphur may exist in within the thermodynamic stability domain of water, as well as to the high lability of many sulphur species, such as the polythionic acids and polysulfides. Additionally, sulphur, along with arsenic, antimony, and mercury, effectively promotes the entry of hydrogen into metal and alloy matrices, thereby leading to hydrogen damage and hydrogen embrittlement. In this paper, the chemistry of sulphur species in aqueous solutions and of the various iron sulphides is reviewed with emphasis on illustrating the diverse nature of metal/sulphur interactions. Finally, we identify a number of critical issues that need to be resolved to greatly improve our understanding of the chemistry of sulphur-containing systems and to improve our ability to predict the form and extent of corrosion in geochemical and geoenergy systems.

  17. Critical issues in the use of metals and alloys in sulphur-containing aqueous systems

    Energy Technology Data Exchange (ETDEWEB)

    Macdonald, D.D.

    1992-01-01

    Sulphur-containing aqueous fluids are amongst the most corrosive environments experienced in industrial and natural systems. The high corrosivity is due principally to the wide range of oxidation states that sulphur may exist in within the thermodynamic stability domain of water, as well as to the high lability of many sulphur species, such as the polythionic acids and polysulfides. Additionally, sulphur, along with arsenic, antimony, and mercury, effectively promotes the entry of hydrogen into metal and alloy matrices, thereby leading to hydrogen damage and hydrogen embrittlement. In this paper, the chemistry of sulphur species in aqueous solutions and of the various iron sulphides is reviewed with emphasis on illustrating the diverse nature of metal/sulphur interactions. Finally, we identify a number of critical issues that need to be resolved to greatly improve our understanding of the chemistry of sulphur-containing systems and to improve our ability to predict the form and extent of corrosion in geochemical and geoenergy systems.

  18. System design description of forced-convection molten-salt corrosion loops MSR-FCL-3 and MSR-FCL-4

    International Nuclear Information System (INIS)

    Molten-salt corrosion loops MSR-FCL-3 and MSR-FCL-4 are high-temperature test facilities designed to evaluate corrosion and mass transfer of modified Hastelloy N alloys for future use in Molten-Salt Breeder Reactors. Salt is circulated by a centrifugal sump pump to evaluate material compatibility with LiF-BeF2-ThF4-UF4 fuel salt at velocities up to 6 m/s (20 fps) and at salt temperatures from 566 to 7050C (1050 to 13000F). The report presents the design description of the various components and systems that make up each corrosion facility, such as the salt pump, corrosion specimens, salt piping, main heaters, salt coolers, salt sampling equipment, and helium cover-gas system, etc. The electrical systems and instrumentation and controls are described, and operational procedures, system limitations, and maintenance philosophy are discussed

  19. Aqueous Transport Code Revisions Using Geographic Information Systems

    International Nuclear Information System (INIS)

    STREAM II, developed at the Savannah River Site (SRS) for execution on a personal computer, is an emergency response code that predicts downstream pollutant concentrations for releases from the SRS area to the Savannah River for emergency response management decision making. The STREAM II code consists of pre-processor, calculation, and post-processor modules. The pre-processor module provides a graphical user interface (GUI) for inputting the initial release data. The GUI passes the user specified data to the calculation module that calculates the pollutant concentrations at downstream locations and the transport times. The calculation module of the STREAM II adopts the transport module of the WASP5 code. WASP5 is a US Environmental Protection Agency water quality analysis program that simulates pollutant transport and fate through surface water using a finite difference method to solve the transport equation. The calculated downstream pollutant concentrations and travel times a re passed to the post-processor for display on the computer screen in graphical and tabular forms. To minimize the user's effort in the emergency situation, the required input parameters are limited to the time and date of release, type of release, location of release, amount and duration of release, and the calculation units. The user, however, could only select one of the seventeen predetermined locations. Hence, STREAM II could not be used for situations in which release locations differ from the seventeen predetermined locations. To eliminate this limitation, STREAM II has been revised to allow users to select the release location anywhere along the specified SRS main streams or the Savannah River by mouse-selection from a map displayed on the computer monitor. The required modifications to STREAM II using geographic information systems (GIS) software is discussed in this paper

  20. Extraction of natural red colorants from the fermented broth of Penicillium purpurogenum using aqueous two-phase polymer systems.

    Science.gov (United States)

    Santos-Ebinuma, Valéria Carvalho; Lopes, André Moreni; Pessoa, Adalberto; Teixeira, Maria Francisca Simas

    2015-01-01

    Safety concerns related to the increasing and widespread application of synthetic coloring agents have increased the demand for natural colorants. Fungi have been employed in the production of novel and safer colorants. In order to obtain the colorants from fermented broth, suitable extraction systems must be developed. Aqueous two-phase polymer systems (ATPPS) offer a favorable chemical environment and provide a promising alternative for extracting and solubilizing these molecules. The aim of this study was to investigate the partitioning of red colorants from the fermented broth of Penicillium purpurogenum using an ATPPS composed of poly(ethylene glycol) (PEG) and sodium polyacrylate (NaPA). Red colorants partitioned preferentially to the top (PEG-rich phase). In systems composed of PEG 6,000 g/mol/NaPA 8,000 g/mol, optimum colorant partition coefficient (KC ) was obtained in the presence of NaCl 0.1 M (KC  = 10.30) while the PEG 10,000 g/mol/NaPA 8,000 g/mol system in the presence of Na2 SO4 0.5 M showed the highest KC (14.78). For both polymers, the mass balance (%MB) and yield in the PEG phase (%ηTOP ) were close to 100 and 79%, respectively. The protein selectivity in all conditions evaluated ranged from 2.0-3.0, which shows a suitable separation of the red colorants and proteins present in the fermented broth. The results suggest that the partitioning of the red colorants is dependent on both the PEG molecular size and salt type. Furthermore, the results obtained support the potential application of ATPPS as the first step of a purification process to recover colorants from fermented broth of microorganisms. PMID:26097197

  1. Integrated extraction and purification of soy isoflavones by using aqueous micellar systems.

    Science.gov (United States)

    Cordisco, Estefanía; Haidar, Carla N; Coscueta, Ezequiel R; Nerli, Bibiana B; Malpiedi, Luciana P

    2016-12-15

    In this work, an integration of solid-liquid and liquid-liquid extractions by using aqueous micellar two-phase systems was evaluated as potential tool to purify soy isoflavones. Additionally, the proposed methodology aimed to preserve the protein content of the processed soy flour. The extractive assays were performed in AMTPS formed by Triton X-114 and sodium tartrate. In order to optimize the purification process, temperature and time were evaluated as independent variables. Under optimal working conditions, i.e. 100min and 33°C of incubation, IF were purified with a recovery percentage of 93 and a purification factor of almost 10. More importantly, the obtained sample presented an aglycone proportion superior to the reported by other methodologies. These results open perspectives to the use of aqueous micellar two-phase systems as an integrative methodology to extract, concentrate and purify isoflavones. PMID:27451211

  2. Quaternary diffusion coefficients in a protein-polymer-salt-water system determined by rayleigh interferometry.

    Science.gov (United States)

    Annunziata, Onofrio; Vergara, Alessandro; Paduano, Luigi; Sartorio, Roberto; Miller, Donald G; Albright, John G

    2009-10-01

    We have experimentally investigated multicomponent diffusion in a protein-polymer-salt-water quaternary system. Specifically, we have measured the nine multicomponent diffusion coefficients, D(ij), for the lysozyme-poly(ethylene glycol)-NaCl-water system at pH 4.5 and 25 degrees C using precision Rayleigh interferometry. Lysozyme is a model protein for protein-crystallization and enzymology studies. We find that the protein diffusion coefficient, D(11), decreases as polymer concentration increases at a given salt concentration. This behavior can be quantitatively related to the corresponding increase in fluid viscosity only at low polymer concentration. However, at high polymer concentration (250 g/L), protein diffusion is enhanced compared to the corresponding viscosity prediction. We also find that a protein concentration gradient induces salt diffusion from high to low protein concentration. This effect increases in the presence of poly(ethylene glycol). Finally, we have evaluated systematic errors associated with measurements of protein diffusion coefficients by dynamic light scattering. This work overall helps characterize protein diffusion in crowded environments and may provide guidance for further theoretical developments in the field of protein crystallization and protein diffusion in such crowded systems, such as the cytoplasm of living cells. PMID:19746957

  3. POTENSI MIKROEMULSI β-KAROTEN DALAM MENGHAMBAT FOTOOKSIDASI VITAMIN C SISTEM AQUEOUS [The Potential Inhibition of Β-Carotene Microemulsion on Vitamin C Photooxidation in Aqueous Systems

    Directory of Open Access Journals (Sweden)

    Setyaningrum Ariviani1*

    2011-06-01

    Full Text Available Photooxidation in food system causes nutritional losses and produces undesirable flavor, toxic and color compounds, which make foods unacceptable to consumers. The objective of this research was to determine β–carotene microemulsion inhibitory effect on vitamin C photooxidation in aqueous food model. Into aqueous food models containing vitamin C (450 ppm for model 1; 300 ppm for model 2 2% microemulsion or β–carotene microemulsion and erythrosine as photosensitizer, were added. The final β–carotene content in aqueous food model was equal to 0.6 or 12 ppm. The result indicated that microemulsion have ability to inhibit vitamin C photodegradation under light but did not show the ability under dark condition. The inhibitory effectiveness of both 6 and 12 ppm β-carotene microemulsion on vitamin C photodegradation were insignificant. The 6 ppm β-carotene microemulsion was proven to effectively inhibit vitamin C photooxidation in aqueous food model better than that of empty microemulsion or free β-carotene. The vitamin C photodegradation rate on model system 1 and 2 were 9.5 ± 2.48 and 6.4 ± 1.58 mg.L-1. hour-1 (β-carotene microemulsion; -14.8 ± 1.69 and -9.5 ± 1.23 mg.L-1. hour -1 (empty microemulsion; -16.0 ± 1.64 and -10.3 ± 0.46 mg.L-1. hour -1 (freeβ-carotene, respectively.

  4. Intermolecular interactions and 3D structure in cellulose-NaOH-urea aqueous system.

    Science.gov (United States)

    Jiang, Zhiwei; Fang, Yan; Xiang, Junfeng; Ma, Yanping; Lu, Ang; Kang, Hongliang; Huang, Yong; Guo, Hongxia; Liu, Ruigang; Zhang, Lina

    2014-08-28

    The dissolution of cellulose in NaOH/urea aqueous solution at low temperature is a key finding in cellulose science and technology. In this paper, (15)N and (23)Na NMR experiments were carried out to clarify the intermolecular interactions in cellulose/NaOH/urea aqueous solution. It was found that there are direct interactions between OH(-) anions and amino groups of urea through hydrogen bonds and no direct interaction between urea and cellulose. Moreover, Na(+) ions can interact with both cellulose and urea in an aqueous system. These interactions lead to the formation of cellulose-NaOH-urea-H2O inclusion complexes (ICs). (23)Na relaxation results confirmed that the formation of urea-OH(-) clusters can effectively enhance the stability of Na(+) ions that attracted to cellulose chains. Low temperature can enhance the hydrogen bonding interaction between OH(-) ions and urea and improve the binding ability of the NaOH/urea/H2O clusters that attached to cellulose chains. Cryo-TEM observation confirmed the formation of cellulose-NaOH-urea-H2O ICs, which is in extended conformation with mean diameter of about 3.6 nm and mean length of about 300 nm. Possible 3D structure of the ICs was proposed by the M06-2X/6-31+G(d) theoretical calculation, revealing the O3H···O5 intramolecular hydrogen bonds could remain in the ICs. This work clarified the interactions in cellulose/NaOH/urea aqueous solution and the 3D structure of the cellulose chain in dilute cellulose/NaOH/urea aqueous solution. PMID:25111839

  5. Application of PEG based aqueous biphasic systems in extraction and separation of no-carrier-added {sup 183}Re from bulk tantalum

    Energy Technology Data Exchange (ETDEWEB)

    Dutta, B.; Lahiri, S. [Saha Institute of Nuclear Physics, Kolkata (India); Tomar, B.S. [Bhabha Atomic Research Centre, Mumbai (India). Radioanalytical Chemistry Div.

    2013-03-01

    No-carrier-added (nca) rhenium isotopes ({sup 182,182m,183}Re) were produced by irradiation with 30 MeV alpha particles on natural tantalum target. The short-lived {sup 182,182m}Re were allowed to decay and long-lived nca {sup 183}Re was separated from bulk tantalum matrix by aqueous biphasic system (ABS) using 2 M solutions of nine different salts, namely, Na{sub 2}SO{sub 4}, Na2SO{sub 3}, NaHSO{sub 3}, Na{sub 2}S{sub 2}O{sub 3}, Na{sub 2}HPO{sub 4}, Na{sub 2}CO{sub 3}, Na-citrate, Na-tartrate, and (NH{sub 4}){sub 2}SO{sub 4} as salt rich phases against 50% (w/w) PEG-4000 as polymer rich phase at room temperature. The influence of temperature and thermodynamic parameters {Delta} H and {Delta} S were obtained for the partition of {sup 183}Re and tantalum in these systems. Nca {sup 183}Re was extracted in high amount in polymer rich phases irrespective of the salt rich phases. Bulk tantalum showed tendency to remain in salt rich phases. ABSs with PEG-4000 polymer rich phase in combination with Na{sub 2}SO{sub 4}, Na{sub 2}SO{sub 3}, NaHSO{sub 3}, Na{sub 2}HPO{sub 4}, Na{sub 2}CO{sub 3}, Na-citrate and Na-tartrate as salt rich phases at basic pH and at ambient temperature (27 C) offered single-step separation between nca {sup 183}Re and bulk Ta. When Na{sub 2}S{sub 2}O{sub 3} and (NH{sub 4}){sub 2}SO{sub 4} were used as salt rich phase, slight extraction of bulk tantalum was observed in PEG-4000 rich phase. The dynamic dissociation constant of {sup 183}Re-PEG-4000 complex was measured by dialysis of the PEG-rich phase against de-ionised water. The k{sub dissociation} value was found as low as 0.0185 min{sup -1}. Therefore, it is possible to have pure {sup 183}Re in de-ionized water immediately after the dialysis. (orig.)

  6. Partitioning Behavior of Papain in Ionic Liquids-Based Aqueous Two-Phase Systems

    OpenAIRE

    Zhiwen Bai; Yanhong Chao; Meiling Zhang; Changri Han; Wenshuai Zhu; Yonghui Chang; Huaming Li; Yang Sun

    2013-01-01

    This paper attempts to study and optimize the affinity partitioning conditions of papain in an aqueous two-phase system (ATPS). The effect of the amount of ionic liquids (ILs), the concentration of K2HPO4, temperature, pH, and the volume of papain solution were discussed concretely. The optimum conditions were determined as ionic liquid was 1.4 g and K2HPO4 was 1.4 g, the extraction efficiency of papain co...

  7. Ruthenium on rutile catalyst, catalytic system, and method for aqueous phase hydrogenations

    Science.gov (United States)

    Elliot, Douglas C.; Werpy, Todd A.; Wang, Yong; Frye, Jr., John G.

    2001-01-01

    An essentially nickel- and rhenium-free catalyst is described comprising ruthenium on a titania support where the titania is greater than 75% rutile. A catalytic system containing a nickel-free catalyst comprising ruthenium on a titania support where the titania is greater than 75% rutile, and a method using this catalyst in the hydrogenation of an organic compound in the aqueous phase is also described.

  8. Calcium Supplementation Improves Na+/K+ Ratio, Antioxidant Defense and Glyoxalase Systems in Salt-Stressed Rice Seedlings

    Science.gov (United States)

    Rahman, Anisur; Nahar, Kamrun; Hasanuzzaman, Mirza; Fujita, Masayuki

    2016-01-01

    The present study investigates the regulatory role of exogenous calcium (Ca) in developing salt stress tolerance in rice seedlings. Hydroponically grown 13-day-old rice (Oryza sativa L. cv. BRRI dhan47) seedlings were exposed to 200 mM NaCl alone and combined with 2 mM CaCl2 and 2 mM ethylene glycol tetraacetic acid (EGTA, a Ca scavenger) for 3 days. The salt stress caused growth inhibition, chlorosis and water shortage in the rice seedlings. The salt-induced stress disrupted ion homeostasis through Na+ influx and K+ efflux, and decreased other mineral nutrient uptake. Salt stress caused oxidative stress in seedlings through lipid peroxidation, loss of plasma membrane integrity, higher reactive oxygen species (ROS) production and methylglyoxal (MG) formation. The salt-stressed seedlings supplemented with exogenous Ca recovered from water loss, chlorosis and growth inhibition. Calcium supplementation in the salt-stressed rice seedlings improved ion homeostasis by inhibition of Na+ influx and K+ leakage. Exogenous Ca also improved ROS and MG detoxification by improving the antioxidant defense and glyoxalase systems, respectively. On the other hand, applying EGTA along with salt and Ca again negatively affected the seedlings as EGTA negated Ca activity. It confirms that, the positive responses in salt-stressed rice seedlings to exogenous Ca were for Ca mediated improvement of ion homeostasis, antioxidant defense and glyoxalase system.

  9. High level nuclear waste repository in salt: Sealing systems status and planning report: Draft report

    Energy Technology Data Exchange (ETDEWEB)

    None

    1985-09-01

    This report documents the initial conceptual design studies for a repository sealing system for a high-level nuclear waste repository in salt. The first step in the initial design studies was to review the current design level, termed schematic designs. This review identified practicality of construction and development of a design methodology as two key issues for the conceptual design. These two issues were then investigated during the initial design studies for seal system materials, seal placement, backfill emplacement, and a testing and monitoring plan. The results of these studies have been used to develop a program plan for completion of the sealing system conceptual design. 60 refs., 26 figs., 18 tabs.

  10. Vapour pressures and densities of the mixed-solvent desiccants (glycols + water + salts)

    International Nuclear Information System (INIS)

    The vapour pressures and densities of the mixed-solvent desiccants have been studied for temperatures ranging from (303.15 to 343.15) K. The mixed-solvent desiccants investigated were aqueous-organic systems with salt. The studied organic solvents were diethylene glycol, tetraethylene glycol, and dipropylene glycol. The chosen salts were lithium chloride and lithium bromide. Six ternaries (glycol/water/salt) were selected for this study. For each ternary system, four systems of which (4-25) mass% salt mixed with various glycols (50-80) mass% were investigated. Incorporated with the pseudo-solvent approach, a vapour pressure model based on the mean spherical approximation for aqueous electrolyte solutions was used to represent the measured vapour pressure of glycol/water/salt systems. A simplified density equation was applied to model the measured density of glycol/water/salt systems. Satisfactory results were obtained for vapour pressure and density calculations. The vapour pressures of the aqueous-organic systems with salt yield smaller values of vapour pressures compared to the conventionally used liquid desiccants. The properties obtained and presented in this study are, in general, of sufficient accuracy for most engineering-design calculations, such as the design of dehumidifier process using mixed-solvent desiccants as absorbents.

  11. Microbiologically induced corrosion of aluminum alloys in fuel-oil/aqueous system.

    Science.gov (United States)

    Yang, S S; Lin, J Y; Lin, Y T

    1998-09-01

    To investigate the microbiologically induced corrosion of aluminum alloys in fuel-oil/aqueous system, aluminum alloys A356, AA 5052, AA 5083 and AA 6061 were chosen as the test alloys and Cladosporium and several fuel-oil contaminated microbes isolated in Taiwan were used as test organisms. Aluminum alloy AA 5083 in fuel-oil/aqueous system was the most susceptible material for microbial corrosion, then followed by aluminum alloys AA 5052 and A356, and AA 6061 was more resistant to microbial aggression. Mixed culture had high capability of corrosion, then followed by Penicillium sp. AM-F5, Fusarium sp. AM-F1, Pseudomonas aeruginosa AM-B5, Ps. fluorescens AM-B9, C. resinae ATCC 22712, Penicillium sp. AM-F2, Candida sp. AM-Y1 and Ps. aeruginosa AM-B11. From energy dispersive spectrometer analysis, aluminum and magnesium contents decreased in the corrosion area, while chlorine and sulfur contents increased. The major organic acid produced in fuel-oil/aqueous system was acetic acid, and the total organic acids content had a positive correlation with the degree of microbial corrosion. PMID:10496152

  12. IUPAC-NIST Solubility Data Series. 100. Rare Earth Metal Fluorides in Water and Aqueous Systems. Part 3. Heavy Lanthanides (Gd–Lu)

    Energy Technology Data Exchange (ETDEWEB)

    Mioduski, Tomasz [Institute of Nuclear Chemistry and Technology, 03195 Warszawa (Poland); Gumiński, Cezary, E-mail: cegie@chem.uw.edu.pl [Department of Chemistry, University of Warsaw, 02093 Warszawa (Poland); Zeng, Dewen, E-mail: dewen-zeng@hotmail.com [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China)

    2015-06-15

    This is the third part of the volume devoted to solubility data for the rare earth metal (REM) fluorides in water and in aqueous ternary and multicomponent systems. It covers experimental results of trivalent fluorides of Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu (so-called heavy lanthanides), since no quantitative data on solubilities of TbF{sub 4} and YbF{sub 2} (the most stable compounds at these valencies) are available. The related literature has been covered through the end of 2014. Compilations of all available papers with the solubility data are introduced for each REM fluoride with a corresponding critical evaluation. Every such assessment contains a collection of all solubility results in aqueous solution, a selection of suggested solubility data, a solubility equation, and a brief discussion of the multicomponent systems. Only simple fluorides (no complexes or double salts) are treated as the input substances in this report. General features of the systems, such as nature of the equilibrium solid phases, solubility as a function of temperature, influence of ionic strength, solution pH, mixed solvent medium on the solubility, quality of the solubility results, and the solubility as a function of REM atomic number, have already been presented in Part 1 of the volume.

  13. Molten Salt Power Tower Cost Model for the System Advisor Model (SAM)

    Energy Technology Data Exchange (ETDEWEB)

    Turchi, C. S.; Heath, G. A.

    2013-02-01

    This report describes a component-based cost model developed for molten-salt power tower solar power plants. The cost model was developed by the National Renewable Energy Laboratory (NREL), using data from several prior studies, including a contracted analysis from WorleyParsons Group, which is included herein as an Appendix. The WorleyParsons' analysis also estimated material composition and mass for the plant to facilitate a life cycle analysis of the molten salt power tower technology. Details of the life cycle assessment have been published elsewhere. The cost model provides a reference plant that interfaces with NREL's System Advisor Model or SAM. The reference plant assumes a nominal 100-MWe (net) power tower running with a nitrate salt heat transfer fluid (HTF). Thermal energy storage is provided by direct storage of the HTF in a two-tank system. The design assumes dry-cooling. The model includes a spreadsheet that interfaces with SAM via the Excel Exchange option in SAM. The spreadsheet allows users to estimate the costs of different-size plants and to take into account changes in commodity prices. This report and the accompanying Excel spreadsheet can be downloaded at https://sam.nrel.gov/cost.

  14. Supra-molecular Association and Polymorphic Behaviour In Systems Containing Bile Acid Salts

    Directory of Open Access Journals (Sweden)

    Camillo La Mesa

    2007-08-01

    Full Text Available A wide number of supra-molecular association modes are observed in mixtures containing water and bile salts, BS, (with, eventually, other components. Molecular or micellar solutions transform into hydrated solids, fibres, lyotropic liquid crystals and/or gels by raising the concentration, the temperature, adding electrolytes, surfactants, lipids and proteins. Amorphous or ordered phases may be formed accordingly. The forces responsible for this very rich polymorphism presumably arise from the unusual combination of electrostatic, hydrophobic and hydrogen-bond contributions to the system stability, with subsequent control of the supra-molecular organisation modes. The stabilising effect due to hydrogen bonds does not occur in almost all surfactants or lipids and is peculiar to bile acids and salts. Some supra-molecular organisation modes, supposed to be related to malfunctions and dis-metabolic diseases in vivo, are briefly reported and discussed.

  15. Constructed wetland treatment systems for the remediation of metal- bearing aqueous discharges. Final report

    International Nuclear Information System (INIS)

    Electric utility activities, such as coal mining, processing, and combustion, often produce aqueous (wastewater) discharges containing metals. Chemical treatment of these discharges to achieve compliance with National Pollution Discharge Elimination System (NPDES) requirements can be costly. Constructed wetland treatment systems offer an inexpensive, natural, low-maintenance, and potentially long-term solution for the treatment of aqueous discharges without chemical additives. At the present time, several electric utilities are using constructed wetland treatment systems to achieve NPDES compliance. Constructed wetland treatment systems take advantage of natural biogeochemical processes to treat utility wastewaters, thus meeting NPDES compliance levels in an environmentally effective manner. This report provides information on the natural science, wastewater treatment, and regulatory/jurisdictional aspects of constructed wetland treatment systems used within the electric utility industry. Included is data from a number of electric utility constructed wetland treatment sites. The principal advantages of using constructed wetland systems to treat wastewater are the low overall cost compared to more conventional chemical treatment methods, the simplicity of operation, and the capacity to provide long-term resource recovery. For example, using a lined constructed wetland treatment system with high retention efficiency for heavy metals provides the option of resource recovery at some future date from a discrete volume of wetland material. Contaminants that can be removed with high efficiency in a number of constructed wetland treatment systems include heavy metals, toxic organics, suspended solids, and nutrients. This report discusses the treatability of specific contaminants as well as metal uptake and translocation processes in constructed wetlands

  16. Cytotoxicity of aqueous extracts of Rosmarinus officinalis L. (Labiatae) in plant test system.

    Science.gov (United States)

    Cardoso, G H S; Dantas, E B S; Sousa, F R C; Peron, A P

    2014-11-01

    This study investigated the cytotoxic activity of Rosmarinus officinalis L. (rosemary) aqueous extract on the cell cycle of Allium cepa. To this end, crude aqueous leaf extracts at four concentrations, 0.02, 0.04, 0.06 and 0.08 mg/mL, were tested on A. cepa meristematic root cells, at exposure times of 24 and 48 h. Slides were prepared by the crushing technique, and cells analyzed throughout the cell cycle, totaling 5,000 for each control group and concentration. The four concentrations tested, including the lowest and considered ideal for use, at all exposure times, showed a significant antiproliferative effect on the cell cycle of this test system and presented a high number of cells in prophase. Our results evidenced the cytotoxicity of rosemary extracts, under the studied conditions. PMID:25627599

  17. Complexes of Al(3), Ga(3) and In(3) ions with sodium salt of morin-5'-sulfonic acid (NaMSA) in aqueous solutions

    International Nuclear Information System (INIS)

    The complexation equilibria of Al(3), Ga(3) and In(3) with NaMSA in acid aqueous solutions have been investigated. The composition and the equilibrium constants of the reaction as well as the concentration stability constants of the complexes have been determined. The probable mechanisms of the complexation reaction have been suggested. (author)

  18. Mature cave systems in salt and their evolution under sea-level oscillations and salt diapir uplif (Persian gulf, Iran)

    Czech Academy of Sciences Publication Activity Database

    Bruthans, J.; Filippi, Michal; Bosák, Pavel; Zare, M.

    Zaragoza: University of Zaragoza, 2005 - (Gutiérrez, F.; Gutiérrez, M.; Desir, G.; Buerrero, J.; Lucha, P.; Marín, C.; García-Ruiz, J.). s. 422-422 [International Conference on Geomorphology /6./ - Geomorphology in regions of environmental contrasts. 07.09.2005-11.09.2005, Zaragoza] R&D Projects: GA AV ČR(CZ) IAB301110501 Institutional research plan: CEZ:AV0Z3013912 Keywords : cave * salt * sea - level oscillations Subject RIV: DB - Geology ; Mineralogy

  19. Molten salt electrolyte separator

    Science.gov (United States)

    Kaun, Thomas D.

    1996-01-01

    A molten salt electrolyte/separator for battery and related electrochemical systems including a molten electrolyte composition and an electrically insulating solid salt dispersed therein, to provide improved performance at higher current densities and alternate designs through ease of fabrication.

  20. Assessment of Effectiveness of Geologic Isolation Systems: REFERENCE SITE INITIAL ASSESSMENT FOR A SALT DOME REPOSITORY

    Energy Technology Data Exchange (ETDEWEB)

    Harwell, M. A.; Brandstetter, A.; Benson, G. L.; Raymond, J. R.; Brandley, D. J.; Serne, R. J.; Soldat, J. K.; Cole, C. R.; Deutsch, W. J.; Gupta, S. K.; Harwell, C. C.; Napier, B. A.; Reisenauer, A. E.; Prater, L. S.; Simmons, C. S.; Strenge, D. L.; Washburn, J. F.; Zellmer, J. T.

    1982-06-01

    As a methodology demonstration for the Office of Nuclear Waste Isolation (ONWI), the Assessment of Effectiveness of Geologic Isolation Systems (AEGIS) Program conducted an initial reference site analysis of the long-term effectiveness of a salt dome repository. The Hainesville Salt Dome in Texas was chosen to be representative of the Gulf Coast interior salt domes; however, the Hainesville Site has been eliminated as a possible nuclear waste repository site. The data used for this exercise are not adequate for an actual assessment, nor have all the parametric analyses been made that would adequately characterize the response of the geosystem surrounding the repository. Additionally, because this was the first exercise of the complete AEGIS and WASTE Rock Interaction Technology (WRIT) methodology, this report provides the initial opportunity for the methodology, specifically applied to a site, to be reviewed by the community outside the AEGIS. The scenario evaluation, as a part of the methodology demonstration, involved consideration of a large variety of potentially disruptive phenomena, which alone or in concert could lead to a breach in a salt dome repository and to a subsequent transport of the radionuclides to the environment. Without waste- and repository-induced effects, no plausible natural geologic events or processes which would compromise the repository integrity could be envisioned over the one-million-year time frame after closure. Near-field (waste- and repository-induced) effects were excluded from consideration in this analysis, but they can be added in future analyses when that methodology development is more complete. The potential for consequential human intrusion into salt domes within a million-year time frame led to the consideration of a solution mining intrusion scenario. The AEGIS staff developed a specific human intrusion scenario at 100 years and 1000 years post-closure, which is one of a whole suite of possible scenarios. This scenario

  1. Assessment of Effectiveness of Geologic Isolation Systems: REFERENCE SITE INITIAL ASSESSMENT FOR A SALT DOME REPOSITORY

    Energy Technology Data Exchange (ETDEWEB)

    Harwell, M. A.; Brandstetter, A.; Benson, G. L.; Bradley, D. J.; Serne, R. J.; Soldat, J. K; Cole, C. R.; Deutsch, W. J.; Gupta, S. K.; Harwell, C. C.; Napier, B. A.; Reisenauer, A. E.; Prater, L. S.; Simmons, C. S.; Strenge, D. L.; Washburn, J. F.; Zellmer, J. T.

    1982-06-01

    As a methodology demonstration for the Office of Nuclear Waste Isolation (ONWI), the Assessment of Effectiveness of Geologic Isolation Systems (AEGIS) Program conducted an initial reference site analysis of the long-term effectiveness of a salt dome repository. The Hainesville Salt Dome in Texas was chosen to be representative of the Gulf Coast interior salt domes; however, the Hainesville Site has been eliminated as a possible nuclear waste repository site. The data used for this exercise are not adequate for an actual assessment, nor have all the parametric analyses been made that would adequately characterize the response of the geosystem surrounding the repository. Additionally, because this was the first exercise of the complete AEGIS and WASTE Rock Interaction Technology (WRIT) methodology, this report provides the initial opportunity for the methodology, specifically applied to a site, to be reviewed by the community outside the AEGIS. The scenario evaluation, as a part of the methodology demonstration, involved consideration of a large variety of potentially disruptive phenomena, which alone or in concert could lead to a breach in a salt dome repository and to a subsequent transport of the radionuclides to the environment. Without waste- and repository-induced effects, no plausible natural geologic events or processes which would compromise the repository integrity could be envisioned over the one-million-year time frame after closure. Near-field (waste- and repository-induced) effects were excluded from consideration in this analysis, but they can be added in future analyses when that methodology development is more complete. The potential for consequential human intrusion into salt domes within a million-year time frame led to the consideration of a solution mining intrusion scenario. The AEGIS staff developed a specific human intrusion scenario at 100 years and 1000 years post-closure, which is one of a whole suite of possible scenarios. This scenario

  2. Single and Tertiary System Dye Removal from Aqueous Solution Using Bottom Ash: Kinetic and Isotherm Studies

    Directory of Open Access Journals (Sweden)

    R. Gandhimathi

    2012-01-01

    Full Text Available This paper investigates the ability of Bottom ash to adsorb three cationic dyes from aqueous solution in single and tertiary systems. Crystal Violet (CV, Methylene Blue (MB and Malachite Green (MG were used as cationic dye models. The surface characteristics of Bottom ash were investigated using Fourier Transform Infrared (FTIR. Pseudo second order model was fitted better than Pseudo First order model for all system of MG, MB and CV. From the isotherm study, the adsorption capacity increased in the order of MB< MGsystem. It may be concluded that the adsorption capacity of Bottom ash decreases in tertiary system as compared to single system. Langmuir and Freundlich isotherm models were fitted for all system of dyes. Freundlich isotherm model found to be the best fit for all systems.

  3. Partition of proteins in aqueous two-phase systems based on Cashew-nut tree gum and poly(ethylene glycol

    Directory of Open Access Journals (Sweden)

    Leonie Asfora Sarubbo

    2004-09-01

    Full Text Available The partitioning of two proteins, bovine serum albumin (BSA and trypsin was studied in an aqueous poly(ethylene glycol(PEG- Cashew-nut tree gum system. The phase diagram was provided for Cashew-nut tree gum and PEG molecular weight of 1500 at two different temperatures. The influence of several parameters including concentrations of polymers, pH, salt addition and temperature on the partitioning of these proteins were investigated.. The results of this research demonstrated the importance of the protein characteristics for partitioning in aqueous biphasic system.A partição de duas proteínas, albumina de soro bovino (BSA e tripsina foi estudada no sistema bifásico aquoso Polietileno glicol(PEG - Goma do cajueiro. O diagrama de fases foi estabelecido para a Goma do Cajueiro e para PEG de peso molecular 1500 em duas diferentes temperaturas. A influência de vários parâmetros na partição destas proteínas, incluindo concentração dos polímeros, pH, adição de sal e temperatura foi investigada. Os resultados desta pesquisa demonstraram a importância das características da proteína na partição em sistemas bifásicos aquosos.

  4. Isotope Fractionation of chlorine in Aqueous System: One Study on Anion-Exchange Chromatography.

    Science.gov (United States)

    Musashi, M.; Oi, T.; Eggenkamp, H.; Van Cappellen, P.

    2001-05-01

    Stable chlorine isotopes such as 37Cl and 35Cl have been paid attention as useful tool identifying the source, and monitoring the transport process and natural fate of chlorinated organic pollutants in air and groundwater. However, it is not established yet whether any isotope effects accompany biodegradation or reductive dehalogenation of the pollutants (Clark and Fritz, 1997). Here we first present an experimental determination of isotope fractionation factor of chlorine in aqueous system by using anion-exchange chromatographic technique. Into the Cl-free anion exchange resin (Muromac, OH- form) packed in a 30 cm long pyrex glass column and controlled temperature at 25 oC, hydrochloric solution was fed with controlling the flow rate constant. Effluent from the column was recovered by an automatic fraction collector and prepared for Cl isotope analysis. The Cl isotope ratio (δ 37Cl vs. SMOC) was measured by IR-MS at the Utrecht University with precision of 0.06 per-mil. Magnitude of the factor obtained was 1.00035 at 25 oC. The result indicates that the lighter isotope (35Cl) was preferably fractionated into the resin phase, while the heavier one (37Cl) was enriched into the aqueous phase. This trend suggests that molecular structure of hydrolysis with Cl in aqueous phase may be more stable than that of Cl ionically bonding with the resin. This result may offer physico-chemical insights into behavior and fate of the pollutants.

  5. Degradation of the herbicide 2, 4-dichlorophenoxyacetic acid (2,4-D) dimethylamine salt by gamma radiation from cobalt-60 in aqueous solution containing humic acid

    International Nuclear Information System (INIS)

    In this study, gamma radiation from cobalt-60 was used to degrade the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) dimethylamine salt in water in the presence of humic acid. The 2,4-D dimethylamine salt 1.13x10-4 mol dm-3 solution was irradiated with different doses. HPLC was used as an analytical technique to determine the degradation rate of herbicide studied. The results showed that the herbicide was completely degraded at an absorbed dose of 3 kGy. Degradation decreased when humic acid was added to all the doses. ESI/MS and MS/MS were used to identify the radiolytic degradation products. A fragmentation path for production of 4.6-dichlororesorcinol, is suggested. The radiolytic yields (G) were calculated

  6. The Significance of Interfacial Water Structure in Soluble Salt Flotation Systems.

    Science.gov (United States)

    Hancer, M.; Celik, M. S.; Miller, J. D.

    2001-03-01

    Flotation of soluble salts with dodecyl amine hydrochloride (DAH) and sodium dodecyl sulfate (SDS) collectors has demonstrated that the interfacial water structure and hydration states of soluble salt surfaces together with the precipitation tendency of the corresponding collector salts are of considerable importance in explaining their flotation behavior. In particular, the high concentration of ions in these soluble salt brines and their hydration appear to modify the bulk and interfacial structure of water as revealed by contact angle measurements and this effect is shown to be an important feature in the flotation chemistry of soluble salt minerals including alkali halide and alkali oxyanion salts. Depending on characteristic chemical features (salt type), the salt can serve either as a structure maker, in which intermolecular hydrogen bonding between water molecules is facilitated, or as a structure breaker, in which intermolecular hydrogen bonding between water molecules is disrupted. For structure making salts the brine completely wets the salt surface and no contact angle can be measured. For structure breaking salts the brine does not completely wet the salt surface and a finite contact angle is measured. In this regard it has been found that soluble salt flotation either with the cationic DAH or anionic SDS collector is possible only if the salt is a structure breaker. Copyright 2001 Academic Press. PMID:11237454

  7. Rapid RNA Exchange in Aqueous Two-Phase System and Coacervate Droplets

    Science.gov (United States)

    Jia, Tony Z.; Hentrich, Christian; Szostak, Jack W.

    2014-02-01

    Compartmentalization in a prebiotic setting is an important aspect of early cell formation and is crucial for the development of an artificial protocell system that effectively couples genotype and phenotype. Aqueous two-phase systems (ATPSs) and complex coacervates are phase separation phenomena that lead to the selective partitioning of biomolecules and have recently been proposed as membrane-free protocell models. We show in this study through fluorescence recovery after photobleaching (FRAP) microscopy that despite the ability of such systems to effectively concentrate RNA, there is a high rate of RNA exchange between phases in dextran/polyethylene glycol ATPS and ATP/poly-L-lysine coacervate droplets. In contrast to fatty acid vesicles, these systems would not allow effective segregation and consequent evolution of RNA, thus rendering these systems ineffective as model protocells.

  8. Comparison of capacitive behavior of activated carbons with different pore structures in aqueous and nonaqueous systems

    Institute of Scientific and Technical Information of China (English)

    ZHOU Shao-yun; LI Xin-hai; WANG Zhi-xing; GUO Hua-jun; PENG Wen-jie

    2008-01-01

    The pore structures of two activated carbons from sawdust with KOH activation and coconut-shell with steam activation for supercapacitor were analyzed by N2 adsorption method. The electrochemical properties of both activated carbons in 6mol/L KOH solution and 1mol/L Et4NPF4/PC were compared, and the effect of pore structure on the capacitance was investigated by cyclic voltammetry, AC impedance and charge-discharge measurements. The results indicate that the capacitance mainly depends on effective surface area, but the power property mainly depends on mesoporosity. At low specific current (1A/g), the maximum specific capacitances of 276.3F/g in aqueous system and 123.9F/g in nonaqueous system can be obtained from sawdust activated carbon with a larger surface area of 1808m2/g, but at a high specific current, the specific capacitance of coconut-shell activated carbon with a higher mesoporosity of 75.1% is more excellent. Activated carbon by KOH activation is fitter for aqueous system and that by steam activation is fitter for nonaqueous system.

  9. Patterns and Determinants of Halophilic Archaea (Class Halobacteria) Diversity in Tunisian Endorheic Salt Lakes and Sebkhet Systems

    OpenAIRE

    Najjari, Afef; Mostafa S Elshahed; Cherif, Ameur; Youssef, Noha H.

    2015-01-01

    We examined the diversity and community structure of members of the halophilic Archaea (class Halobacteria) in samples from central and southern Tunisian endorheic salt lakes and sebkhet (also known as sebkha) systems using targeted 16S rRNA gene diversity survey and quantitative PCR (qPCR) approaches. Twenty-three different samples from four distinct locations exhibiting a wide range of salinities (2% to 37%) and physical characteristics (water, salt crust, sediment, and biofilm) were examin...

  10. Reductive extraction equilibrium of f-elements in the molten salt and liquid metal binary phase system

    International Nuclear Information System (INIS)

    Equilibrium distribution of lanthanides and actinides were experimentally determined in the binary phase system consisting of molten alkaline chloride salt and liquid metal. By analyzing the observed distribution ratio of solutes between salt phase and liquid Zn and Bi, thermodynamic constants of alloy formation of lanthanides and actinides with Zn and Bi were obtained. On the observed result, the systematics of lanthanides in their alloy formation with Zn and Bi was discussed and different systematics of actinides was discussed. (author)

  11. Influence of pH, inorganic anions, and dissolved organic matter on the photolysis of antimicrobial triclocarban in aqueous systems under simulated sunlight irradiation.

    Science.gov (United States)

    Ding, Shi-Ling; Wang, Xi-Kui; Jiang, Wen-Qiang; Zhao, Ru-Song; Shen, Ting-Ting; Wang, Chen; Wang, Xia

    2015-04-01

    The photolysis of the antimicrobial triclocarban (TCC) in aqueous systems under simulated sunlight irradiation was studied. The effects of several abiotic parameters, including solution pH, initial TCC concentration, presence of natural organic matter, and most common inorganic anions in surface waters, were investigated. The results show that the photolysis of TCC followed pseudo-first-order kinetics. The TCC photolysis rate constant increased with increasing solution pH and decreasing the initial TCC concentration. Compared with the TCC photolysis in pure water, the presence of aqueous bicarbonate, nitrate, humic acids, and its sodium salt decreased the TCC photolysis rate, but fulvic acid increased the TCC photolysis rate. The electron spin resonance and reactive oxygen species scavenging experiments indicated that TCC may undergo two different types of phototransformation reactions: direct photolysis and energy transfer to generate (1)O2. The main degradation products were tentatively identified by gas chromatography interfaced with mass spectrometry (GC-MS), and a possible degradation pathway was also proposed. PMID:25354431

  12. SYSNET: A salt-site systems network model for scenario assessments

    International Nuclear Information System (INIS)

    This document contains a description of the initial version of the systems model SYSNET. This model is being developed to analyze potentially disruptive scenarios of salt repository systems. Currently the model features a general three-dimensional network topology and simulates the processes of flow, heat transport in rock, heat transport in fluid, brine transport, salt creep dissolution, and precipitation. Of necessity, the SYSNET Code uses relatively simple semi-analytic algorithms so that it may be implemented statistically. Uncertain parameters may be sampled with a compatible preprocessor and then analyzed statistically with a compatible postprocessor. When used in this fashion, SYSNET may be caused to calculate distributions of various performance measures and sensitivities of performance measures to uncertain parameters. The ultimate objective of the SYSNET development is to prioritize data needs by computing sensitivities relative to a particular performance measure, namely the 10,000-year cumulative release, and to evaluate repository systems for compliance with the US Environmental Protection Agency (EPA) Standard. 16 refs., 25 figs., 31 tabs

  13. Optimization of Biosorptive Removal of Dye from Aqueous System by Cone Shell of Calabrian Pine

    OpenAIRE

    Fatih Deniz

    2014-01-01

    The biosorption performance of raw cone shell of Calabrian pine for C.I. Basic Red 46 as a model azo dye from aqueous system was optimized using Taguchi experimental design methodology. L9 (33) orthogonal array was used to optimize the dye biosorption by the pine cone shell. The selected factors and their levels were biosorbent particle size, dye concentration, and contact time. The predicted dye biosorption capacity for the pine cone shell from Taguchi design was obtained as 71.770 mg g−1 un...

  14. Purification and In Situ Immobilization of Papain with Aqueous Two-Phase System

    OpenAIRE

    Li, Mingliang; Su, Erzheng; You, Pengyong; Gong, Xiangyu; Sun, Ming; Xu, Diansheng; Wei, Dongzhi

    2010-01-01

    Papain was purified from spray-dried Carica papaya latex using aqueous two-phase system (ATPS). Then it was recovered from PEG phase by in situ immobilization or preparing cross-linked enzyme aggregates (CLEAs). The Plackett-Burman design and the central composite design (CCD) together with the response surface methodology (RSM) were used to optimize the APTS processes. The highly purified papain (96–100%) was achieved under the optimized conditions: 40% (w/w) 15 mg/ml enzyme solution, 14.33–...

  15. Analysis and modeling of alkali halide aqueous solutions

    DEFF Research Database (Denmark)

    Kim, Sun Hyung; Anantpinijwatna, Amata; Kang, Jeong Won;

    2016-01-01

    calculations for various electrolyte properties of alkali halide aqueous solutions such as mean ionic activity coefficients, osmotic coefficients, and salt solubilities. The model covers highly nonideal electrolyte systems such as lithium chloride, lithium bromide and lithium iodide, that is, systems that are...... very soluble in water, for example, up to more than 30 mol kg-1. Phase behaviors for the systems are analyzed at concentrations of salt up to the solubility in water at temperatures between 273 and 373 K by comparing calculated results with available experimental data and available models....

  16. The interaction between oxytetracycline and divalent metal ions in aqueous and mixed solvent systems.

    Science.gov (United States)

    Tongaree, S; Flanagan, D R; Poust, R I

    1999-01-01

    The effects of pH, mixed solvent systems, and divalent metal ions on oxytetracycline (OTC) solubility and the interactions between OTC and metal ions in aqueous and mixed solvent systems were investigated. OTC solubility profiles were obtained for pH 4-9. The cosolvents studied were glycerin, propylene glycol, PEG 400, and 2-pyrrolidone with the following metal ions: magnesium, calcium, and zinc. OTC and its interactions with these metal ions were evaluated by solubility, NMR, circular dichroism (CD), and electron diffraction (ED) methods. At pH 5.6, no complexation occurred with these metal ions, but OTC zwitterion formed aggregates in aqueous solutions as shown by NMR spectra. The hydration of the metal ions was observed to affect OTC aggregation, with Mg+2 causing the greatest OTC aggregation. At pH 7.5, OTC aggregation and metal-OTC complexation were observed in solutions with Ca+2 and Mg+2. Zinc ion was found to decrease OTC solubility because of zincate formation, which caused anionic OTC to precipitate. Electron diffraction revealed a relationship between OTC and metal-OTC complex crystallinity and solubility behavior. The zinc-OTC complex exhibited the highest crystallinity and lowest solubility at pH 8.0. Various cosolvents generally enhanced OTC solubility, with 2-pyrrolidone having the best solubility power. In OTC-metal-2-pyrrolidone and OTC-Zn(+2)-PEG 400 systems, circular dichroism provided evidence for the formation of soluble ternary complexes. PMID:10578513

  17. Bifunctional polyacrylonitrile fiber-mediated conversion of sucrose to 5-hydroxymethylfurfural in mixed-aqueous systems.

    Science.gov (United States)

    Shi, Xian-Lei; Zhang, Min; Lin, Huikun; Tao, Minli; Li, Yongdan; Zhang, Wenqin

    2015-03-01

    A highly efficient catalytic system composed of a bifunctional polyacrylonitrile fiber (PANF-PA[BnBr]) and a metal chloride was employed to produce 5-hydroxymethylfurfural (HMF) from sucrose in mixed-aqueous systems. The promoter of PANF-PA[BnBr] incorporates protonic acid groups that promote the hydrolysis of the glycosidic bond to convert sucrose into glucose and fructose, and then catalyzes fructose dehydration to HMF, while the ammonium moiety may promote synergetically with the metal chloride the isomerization of glucose to fructose and transfer HMF from the aqueous to the organic phase. The detailed characterization by elemental analysis, FTIR spectroscopy, and SEM confirmed the rangeability of the fiber promoter during the modification and utilization processes. Excellent results in terms of high yield (72.8%) of HMF, superior recyclability (6 cycles) of the process, and effective scale-up and simple separation procedures of the catalytic system were obtained. Moreover, the prominent features (high strength, good flexibility, etc.) of the fibers are very attractive for fix-bed reactor. PMID:25573698

  18. On-chip aqueous two-phase system (ATPS) formation, consequential self-mixing, and their influence on drop-to-drop aqueous two-phase extraction kinetics

    Science.gov (United States)

    Wijethunga, Pavithra A. L.; Moon, Hyejin

    2015-09-01

    Aqueous two-phase systems (ATPSs) allow an advantageous aqueous two-phase extraction process (ATPE), a special type of liquid-liquid extraction. Compared with conventional liquid-liquid extraction using aqueous/organic extraction media, ATPE is known to provide relatively easy mass transfer and a gentle environment for biological separation applications. Considering the recent interest in microscale ATPE, we aimed to study (i) the potential of preparing ATPS droplets on a digital microfluidic device, and (ii) the influence of the fluidic dynamics created during the formation of ATPS, with the goal of enhancing on-chip ATPE process. On-chip ATPS formation was evaluated by preparing a series of ATPSs on electrowetting on dielectric digital microfluidic chips and comparing their characteristics with the same ATPSs prepared at macroscale using conventional procedures. An enhanced on-chip drop-to-drop ATPE process was achieved by incorporating a self-mixing condition created during ATPSformation. Results indicate a successful on-chip ATPS preparation as well as enhanced extraction performance by self-mixing in the absence of forced mixing. Findings of this research suggest an alternative, simple, yet adequate technique to provide mixing for on-chip applications, such as sample preparation in portable microfluidics, for which it is unfavorable to implement complicated mixing sequences or complex device geometries.

  19. Fish assemblages in Tanzanian mangrove creek systems influenced by solar salt farm constructions

    Science.gov (United States)

    Mwandya, Augustine W.; Gullström, Martin; Öhman, Marcus C.; Andersson, Mathias H.; Mgaya, Yunus D.

    2009-04-01

    Deforestation of mangrove forests is common occurrence worldwide. We examined fish assemblage composition in three mangrove creek systems in Tanzania (East Africa), including two creeks where the upper parts were partly clear-cut of mangrove forest due to the construction of solar salt farms, and one creek with undisturbed mangrove forest. Fish were caught monthly for one year using a seine net (each haul covering 170 m 2) within three locations in each creek, i.e. at the upper, intermediate and lower reaches. Density, biomass and species number of fish were lower in the upper deforested sites compared to the mangrove-fringed sites at the intermediate and lower parts in the two creeks affected by deforestation, whereas there were no differences among the three sites in the undisturbed mangrove creek system. In addition, multivariate analyses showed that the structure of fish assemblages varied between forested and clear-cut sites within the two disturbed creeks, but not within the undisturbed creek. Across the season, we found no significant differences except for a tendency of a minor increase in fish densities during the rainy season. At least 75% of the fishes were juveniles and of commercial interest for coastal fisheries and/or aquaculture. Mugil cephalus, Gerres oyena and Chanos chanos were the most abundant species in the forested sites. The dominant species in the clear-cut areas were M. cephalus and Elops machnata, which were both found in relatively low abundances compared to the undisturbed areas. The conversion of mangrove forests into solar salt farms not only altered fish assemblage composition, but also water and sediment conditions. In comparison with undisturbed areas, the clear-cut sites showed higher salinity, water temperature as well as organic matter and chlorophyll a in the sediments. Our results suggest that mangrove habitat loss and changes in environmental conditions caused by salt farm developments will decrease fish densities, biomass

  20. Electrochemistry of LiCl-Li2O-H2O Molten Salt Systems

    Energy Technology Data Exchange (ETDEWEB)

    Natalie J. Gese; Batric Pesic

    2013-03-01

    Uranium can be recovered from uranium oxide (UO2) spent fuel through the combination of the oxide reduction and electrorefining processes. During oxide reduction, the spent fuel is introduced to molten LiCl-Li2O salt at 650 degrees C and the UO2 is reduced to uranium metal via two routes: (1) electrochemically, and (2) chemically by lithium metal (Li0) that is produced electrochemically. However, the hygroscopic nature of both LiCl and Li2O leads to the formation of LiOH, contributing hydroxyl anions (OH-), the reduction of which interferes with the Li0 generation required for the chemical reduction of UO2. In order for the oxide reduction process to be an effective method for the treatment of uranium oxide fuel, the role of moisture in the LiCl-Li2O system must be understood. The behavior of moisture in the LiCl-Li2O molten salt system was studied using cyclic voltammetry, chronopotentiometry and chronoamperometry, while reduction to hydrogen was confirmed with gas chromatography.

  1. Electrochemistry of molten salt systems within context of modern nuclear fuel cycles

    International Nuclear Information System (INIS)

    Among other applications, electrochemical based separation of actinides and lanthanides from molten salt media seems to be suitable method for reprocessing schemes in several fuel cycles of modern reactor types which are currently under development. Within this work, electrochemical properties of selected actinides (U,Th), lanthanides (Eu, Sm, Nd, Pr, Gd, La) and other elements (Mo, Zr) were studied in several molten fluoride systems (LiF-BeF2, LiF-CaF2, LiF-NaF, LiF-NaF-KF). Based on obtained results, electrolytic experiments to deposit some of the elements on inert and reactive electrode were performed. LiF-BeF2 (FLiBe) melt is considered to be a crucial system for most of the molten salt reactor (MSR) concepts. In FLiBe, basic electrochemical properties of selected actinides and lanthanides were studied. Due to FLiBe's narrow electrochemical window, only uranium can be directly deposited on the cathode. Electrolytic deposition of uranium on Mo and Ni electrodes was achieved. In BeF2-free melts, full spectrum of available elements was studied by variety of electrochemical methods. Electrolytic experiments were performed with special attention given to pulsed-current electrolysis and reactive electrode (Ni) on which the deposits are in the form of alloys and successful separation of uranium from gadolinium was demonstrated. (author)

  2. Calculation of NaCl, KCl and LiCl Salts Activity Coefficients in Polyethylene Glycol (PEG4000)-Water System Using Modified PHSC Equation of State, Extended Debye-Hückel Model and Pitzer Model

    Science.gov (United States)

    Marjani, Azam

    2016-07-01

    For biomolecules and cell particles purification and separation in biological engineering, besides the chromatography as mostly applied process, aqueous two-phase systems (ATPS) are of the most favorable separation processes that are worth to be investigated in thermodynamic theoretically. In recent years, thermodynamic calculation of ATPS properties has attracted much attention due to their great applications in chemical industries such as separation processes. These phase calculations of ATPS have inherent complexity due to the presence of ions and polymers in aqueous solution. In this work, for target ternary systems of polyethylene glycol (PEG4000)-salt-water, thermodynamic investigation for constituent systems with three salts (NaCl, KCl and LiCl) has been carried out as PEG is the most favorable polymer in ATPS. The modified perturbed hard sphere chain (PHSC) equation of state (EOS), extended Debye-Hückel and Pitzer models were employed for calculation of activity coefficients for the considered systems. Four additional statistical parameters were considered to ensure the consistency of correlations and introduced as objective functions in the particle swarm optimization algorithm. The results showed desirable agreement to the available experimental data, and the order of recommendation of studied models is PHSC EOS > extended Debye-Hückel > Pitzer. The concluding remark is that the all the employed models are reliable in such calculations and can be used for thermodynamic correlation/predictions; however, by using an ion-based parameter calculation method, the PHSC EOS reveals both reliability and universality of applications.

  3. Aqueous systems of ethanolamine hydrochlorides and of chlorides of cerium, terbium, dysprosium, erbium

    International Nuclear Information System (INIS)

    The isothermal method of cross sections has been used to study the solubility at 25 and 50 deg C in ternary water-salt systems consisting of cerium chloride and mono-(1), di-(2) and triethanolamine (3) hydrochlorides as well as diethanolamine hydrochloride and terbium, dysprosium and erbium chlorides. Solubility isotherms testify to the formation in the system (1) of a congruently dissolved compound of the CeCl3x2(C2H4OHNN2HCl)x2H2O composition. Individual peculiarities of a new solid phase are proved by the DTA method by means of derivatograph ODL-106, while the composition is confirmed by chemical analysis. The rest of the systems - are of simple eutonic type

  4. Effects of a Pre-Filter and Electrolysis Systems on the Reuse of Brine in the Chinese Cabbage Salting Process.

    Science.gov (United States)

    Kim, Dong-Ho; Yoo, Jae Yeol; Jang, Keum-Il

    2016-06-01

    In this study, the effects of a pre-filter system and electrolysis system on the safe and efficient reuse of brine in the cabbage salting process were investigated. First, sediment filter-electrolyzed brine (SF-EB) was selected as brine for reuse. Then, we evaluated the quality and microbiological properties of SF-EB and Chinese cabbage salted with SF-EB. The salinity (9.4%) and pH (4.63) of SF-EB were similar to those of control brine (CB). SF-EB turbidity was decreased (from 0.112 to 0.062) and SF-EB residual chlorine (15.86 ppm) was higher than CB residual chlorine (0.31 ppm), and bacteria were not detected. Salinity (2.0%), pH (6.21), residual chlorine (0.39 ppm), chromaticity, hardness, and chewiness of cabbage salted with SF-EB were similar to those of cabbage salted with CB. The total bacterial count in cabbage salted with CB was increased as the number of reuses increased (from 6.55 to 8.30 log CFU/g), whereas bacteria in cabbage salted with SF-EB was decreased (from 6.55 to 5.21 log CFU/g). These results show that SF-EB improved the reusability of brine by removing contaminated materials and by sterilization. PMID:27390732

  5. Effects of a Pre-Filter and Electrolysis Systems on the Reuse of Brine in the Chinese Cabbage Salting Process

    Science.gov (United States)

    Kim, Dong-Ho; Yoo, Jae Yeol; Jang, Keum-Il

    2016-01-01

    In this study, the effects of a pre-filter system and electrolysis system on the safe and efficient reuse of brine in the cabbage salting process were investigated. First, sediment filter-electrolyzed brine (SF-EB) was selected as brine for reuse. Then, we evaluated the quality and microbiological properties of SF-EB and Chinese cabbage salted with SF-EB. The salinity (9.4%) and pH (4.63) of SF-EB were similar to those of control brine (CB). SF-EB turbidity was decreased (from 0.112 to 0.062) and SF-EB residual chlorine (15.86 ppm) was higher than CB residual chlorine (0.31 ppm), and bacteria were not detected. Salinity (2.0%), pH (6.21), residual chlorine (0.39 ppm), chromaticity, hardness, and chewiness of cabbage salted with SF-EB were similar to those of cabbage salted with CB. The total bacterial count in cabbage salted with CB was increased as the number of reuses increased (from 6.55 to 8.30 log CFU/g), whereas bacteria in cabbage salted with SF-EB was decreased (from 6.55 to 5.21 log CFU/g). These results show that SF-EB improved the reusability of brine by removing contaminated materials and by sterilization. PMID:27390732

  6. Treatment of plutonium process residues by molten salt oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Stimmel, J.; Wishau, R.; Ramsey, K.B.; Montoya, A.; Brock, J. [Los Alamos National Lab., NM (United States); Heslop, M. [Naval Surface Warfare Center (United States). Indian Head Div.; Wernly, K. [Molten Salt Oxidation Corp. (United States)

    1999-04-01

    Molten Salt Oxidation (MSO) is a thermal process that can remove more than 99.999% of the organic matrix from combustible {sup 238}Pu material. Plutonium processing residues are injected into a molten salt bed with an excess of air. The salt (sodium carbonate) functions as a catalyst for the conversion of the organic material to carbon dioxide and water. Reactive species such as fluorine, chlorine, bromine, iodine, sulfur, phosphorous and arsenic in the organic waste react with the molten salt to form the corresponding neutralized salts, NaF, NaCl, NaBr, NaI, Na{sub 2}SO{sub 4}, Na{sub 3}PO{sub 4} and NaAsO{sub 2} or Na{sub 3}AsO4. Plutonium and other metals react with the molten salt and air to form metal salts or oxides. Saturated salt will be recycled and aqueous chemical separation will be used to recover the {sup 238}Pu. The Los Alamos National Laboratory system, which is currently in the conceptual design stage, will be scaled down from current systems for use inside a glovebox.

  7. Treatment of plutonium process residues by molten salt oxidation

    International Nuclear Information System (INIS)

    Molten Salt Oxidation (MSO) is a thermal process that can remove more than 99.999% of the organic matrix from combustible 238Pu material. Plutonium processing residues are injected into a molten salt bed with an excess of air. The salt (sodium carbonate) functions as a catalyst for the conversion of the organic material to carbon dioxide and water. Reactive species such as fluorine, chlorine, bromine, iodine, sulfur, phosphorous and arsenic in the organic waste react with the molten salt to form the corresponding neutralized salts, NaF, NaCl, NaBr, NaI, Na2SO4, Na3PO4 and NaAsO2 or Na3AsO4. Plutonium and other metals react with the molten salt and air to form metal salts or oxides. Saturated salt will be recycled and aqueous chemical separation will be used to recover the 238Pu. The Los Alamos National Laboratory system, which is currently in the conceptual design stage, will be scaled down from current systems for use inside a glovebox

  8. Effect of bentonite on radiation induced dissolution of UO{sub 2} in an aqueous system

    Energy Technology Data Exchange (ETDEWEB)

    Barreiro Fidalgo, Alexandre, E-mail: alebf@kth.se; Sundin, Sara, E-mail: saramara@kth.se; Jonsson, Mats, E-mail: matsj@kth.se

    2014-04-01

    In order to elucidate the impact of bentonite on the process of radiation induced oxidative dissolution of UO{sub 2} in an aqueous system, the dissolution of U(VI) and consumption of H{sub 2}O{sub 2} over time has been studied. In addition, γ-irradiation experiments were performed to study a more relevant and complex system, serving as a comparison with the previously stated system. In both cases, the experiments revealed that the presence of bentonite in water could either delay or prevent in part the release of uranium to the environment. The cause is mainly attributed to the scavenging of radiolytic oxidants rather than to the adsorption of uranium onto bentonite.

  9. Radiation-chemical behavior of uranium and plutonium in heterogeneous MeO2-aqueous solution systems

    International Nuclear Information System (INIS)

    The paper studies radiation-chemical behavior of U and Pu in heterogeneous UO2-aqueous mellitate systems and the PuO2-groundwater systems, respectively. It is found that U(IV) passes into the aqueous phase in the irradiated system and oxidizes further to U(VI) while Pu(IV) solubilizes both in irradiated and unirradiated groundwater and then goes to Pu(V) and Pu(III). The latter processes is more powerful in irradiated solutions. The radiation-chemical behavior of U and Pu in the systems under study is interpreted on the strength of spectrophotometric characteristics of irradiated and unirradiated solutions. (author)

  10. Oxidation and mobilization of metallic antimony in aqueous systems with simulated groundwater

    Science.gov (United States)

    Ilgen, A. G.; Majs, F.; Barker, A. J.; Douglas, T. A.; Trainor, T. P.

    2014-05-01

    Antimony (Sb) is a contaminant of concern that can be present in elevated concentrations in shooting range soils due to mobilization from spent lead/antimony bullets. Antimony in shooting range soils has been observed as either metallic Sb(0) or as Sb(V) immobilized by iron (hydr)oxides. The absence of Sb(III) in soils is indicative of rapid Sb(III) oxidation to Sb(V) under surface soil conditions. However, the major controls on antimony oxidation and mobility are poorly understood. To better understand these controls we performed multiple batch experiments under oxic conditions to quantify the oxidation and dissolution of antimony in systems where Sb(0) is oxidized to Sb(III) and further to Sb(V). We also tested how variations in the aqueous matrix composition and the presence of metallic lead (Pb) affect the dissolution, solid phase speciation, and oxidation of antimony. We monitored changes in the aqueous antimony speciation using liquid chromatography inductively coupled plasma mass spectrometry (LC-ICP-MS). To test which solid phases form as a result of Sb(0) oxidation, and therefore potentially limit the mobility of antimony in our studied systems, we characterized the partially oxidized Sb(0) powders by means of extended X-ray absorption fine structure (EXAFS) spectroscopy and powder X-ray diffraction (XRD).

  11. Molar heat capacities of some aqueous (2-amino-2-hydroxymethyl-1,3-propanediol + glycol) systems

    International Nuclear Information System (INIS)

    Highlights: ► The molar heat capacities for several aqueous (2-amino-2-hydroxymethyl-1,3-propanediol + glycol) systems were measured. ► The glycols considered were ethylene glycols and propylene glycols. ► The temperature studied was (30 to 70) °C. ► The measured data were reported as functions of temperature and composition. ► The measured data were represented satisfactorily by the applied correlations. - Abstract: A new set of molar heat capacity data for aqueous {2-amino-2-hydroxymethyl-1,3-propanediol (TRIS) + glycol} at (30 to 80) °C and different concentrations (4% to 16% by weight TRIS or 56% to 44% by weight water, in a fixed amount of glycol – 40% by weight) were gathered via reliable measurement method and are presented in this report. The glycols considered were diethylene glycol (DEG), triethylene glycol (TEG), tetraethylene glycol (T4EG), propylene glycol (PG), dipropylene glycol (DPG), and tripropylene glycol (TPG). The 198 data points gathered fit the equation, Cp = Cp,a + B1m + B2m2 + B3m3, where Cp and Cp,a are the molar heat capacities of the (TRIS + glycol + water) and (water + glycol) systems, respectively, Bi the temperature-dependent parameters, and m the mole TRIS per kilogram (glycol + water). The overall average absolute deviation (AAD) of the experimental data from the corresponding values calculated from the correlation equation was 0.07%.

  12. Fluoride partitioning R and D programme for molten salt transmutation reactor systems in the Czech Republic

    Energy Technology Data Exchange (ETDEWEB)

    Uhlir, J. [Nuclear Research Institute Rez plc, CZ (Czech Republic); Priman, V.; Vanicek, J. [Czech Power Company, Praha (Czech Republic)

    2001-07-01

    The transmutation of spent nuclear fuel is considered a prospective alternative conception to the current conception based on the non-reprocessed spent fuel disposal into underground repository. The Czech research and development programme in the field of partitioning and transmutation is founded on the Molten Salt Transmutation Reactor system concept with fluoride salts based liquid fuel, the fuel cycle of which is grounded on pyrochemical / pyrometallurgical fluoride partitioning of spent fuel. The main research activities in the field of fluoride partitioning are oriented mainly towards technological research of Fluoride Volatility Method and laboratory research on electro-separation methods from fluoride melts media. The Czech national conception in the area of P and T research issues from the national power industry programme and from the Czech Power Company intentions of the extensive utilization of nuclear power in our country. The experimental R and D work is concentrated mainly in the Nuclear Research Institute Rez plc that plays a role of main nuclear research workplace for the Czech Power Company. (author)

  13. Fluoride partitioning R and D programme for molten salt transmutation reactor systems in the Czech Republic

    International Nuclear Information System (INIS)

    The transmutation of spent nuclear fuel is considered a prospective alternative conception to the current conception based on the non-reprocessed spent fuel disposal into underground repository. The Czech research and development programme in the field of partitioning and transmutation is founded on the Molten Salt Transmutation Reactor system concept with fluoride salts based liquid fuel, the fuel cycle of which is grounded on pyrochemical / pyrometallurgical fluoride partitioning of spent fuel. The main research activities in the field of fluoride partitioning are oriented mainly towards technological research of Fluoride Volatility Method and laboratory research on electro-separation methods from fluoride melts media. The Czech national conception in the area of P and T research issues from the national power industry programme and from the Czech Power Company intentions of the extensive utilization of nuclear power in our country. The experimental R and D work is concentrated mainly in the Nuclear Research Institute Rez plc that plays a role of main nuclear research workplace for the Czech Power Company. (author)

  14. Thermal storage performance of molten salt thermocline system with packed phase change bed

    International Nuclear Information System (INIS)

    Highlights: • Molten salt thermocline storage with packed phase change bed is simulated. • Phase change material can remarkably increase the effective discharging energy. • Thermocline can be divided into three stages including phase change layer. • Melting point of phase change material should be slightly below initial temperature. • The discharging efficiency increases with the phase change material content. - Abstract: Comprehensive transient and two-dimensional numerical model is developed to study energy storage performance of molten salt thermocline thermal storage system with packed phase change bed in solar thermal power. The results show that the packed phase change bed can remarkably increase the effective discharging energy and discharging efficiency. Because of phase change material, the thermocline can be divided into three stages including the high temperature thermocline, low temperature thermocline and phase change layer. As the melting point within the inlet and initial temperature increases, the whole discharging time decreases, while the effective discharging energy remarkably increases, and thus the melting point of phase change material should be within the initial temperature and effective outlet temperature for good heat storage performance. As the phase change material content increases, the effective discharging energy increases with the effective discharging time rising, and the effective discharging efficiency also increases

  15. Effect of sand and moisture on molten salt properties for open direct absorption solar receiver/storage system

    Science.gov (United States)

    AlQaydi, M. S.; Delclos, T.; AlMheiri, S.; McKrell, T.; Calvet, N.

    2016-05-01

    Solar Salt (60 wt. % sodium nitrate, 40 wt. % potassium nitrate) is one candidate salt mixture for the CSPonD Demo project (Concentrated Solar Power On Demand Demonstration), ongoing collaboration between Masdar Institute and MIT. One prototype is under preparation at the Masdar Institute Solar Platform in Abu Dhabi. In this new concept, the salt will be used as an open direct absorption solar receiver integrated with a storage system so that the effects of dust/sand and moisture on the thermophysical properties have to be investigated. Thermal Gravimetric Analysis (TGA) was used to study the thermal stability and mass loss, while a Differential Scanning Calorimeter (DSC) was used to study the thermal properties and heat capacity of the salt mixture with and without sand. Considering the worst case scenario, the maximum mass loss rate at 550 °C, and in a fully open configuration, was measured to be 0.29 % per hour, around 2.34 per day of use (8 h of operation). The effect of sand was the same under nitrogen gas environment and air with moisture, which resulted in decreasing the melting temperature of the salts mixture and increasing its freezing temperature. The thermal properties remained stable even after 3 temperature cycles with impurities. Finally, the salt heat capacity increased due to the addition of 2 wt. % of sand.

  16. Selective separation and enrichment of proteins in aqueous two-phase extraction system

    Institute of Scientific and Technical Information of China (English)

    Feng Qu; Hao Qin; Min Dong; Dong Xu Zhao; Xin Ying Zhao; Jing Hua Zhang

    2009-01-01

    A simple aqueous two-phase extraction system(ATPS)of PEG/phosphate was proposed for selective separation and enrichment of proteins.The combination of ATPE with HPLC was applied to identify the partition of proteins in two phases.Five proteins (bovine serum albumin,Cytochrome C,lysozyme,myoglobin,and trypsin)were used as model proteins to study the effect of phosphate concentration and pH on proteins partition.The PEG/phosphate system was firstly applied to real human saliva and plasma samples,some proteins showed obviously different partition in two phases.The primary results manifest the selective separation and enrichment of proteins in ATPS provided the potential for high abundance proteins depletion in proteomics.

  17. Dynamics of macroscopic fluctuations in aqueous systems according to Rayleigh scattering data

    Science.gov (United States)

    Belovolova, L. V.; Glushkov, M. V.; Timashev, S. F.

    2015-09-01

    The general question of the existence of macrofluctuations of physical characteristics of aqueous systems are discussed. Using the example of analyzing fluctuations in the Rayleigh scattering of natural untreated water, along with catholyte and anolyte obtained in its electrochemical treatment, the possibility of obtaining of quantitative information on the states and dynamics of changes in such systems is shown. Data on the parameters of oscillations in the Rayleigh light scattering of water catholyte and anolyte immediately after electrolysis, and one and two days after its completion, are presented. Calculations are performed using the general phenomenological approach to analyzing chaotic signals (flicker-noise spectroscopy). Quantitative characteristics that reveal substantial differences in the dynamics of macrofluctuations that develop in the catholyte and anolyte of the studied water are presented.

  18. Successful full-scale deployments of advanced PGPR enhanced phytoremediation systems (PEPS) for decontamination of petroleum and salt impacted soils

    Energy Technology Data Exchange (ETDEWEB)

    Greenberg, B.; Huang, X.D.; Gerhardt, K.; Yu, X.M.; Liddycoat, S.; Lu, X.; Nykamp, J.; McCallum, B.; MacNeill, G.; Mosley, P.; Gurska, J.; Knezevich, N.; Zhong, H.; Gerwing, P. [Waterloo Univ., ON (Canada)

    2010-07-01

    This PowerPoint presentation described a phytoremediation system designed to remediate salt and petroleum contaminated sites. Phytoremediation techniques are cheaper than traditional methods of remediating soils. The phytoremediation process is comprised of volatilization, phytodegradation, and chelation processes. Plants uptake contaminants via a rhizodegradation process. The plants provide biomass for rapid remediation with a restoration time frame of between 2 to 3 years. PGPR enhanced phytoremediation systems (PEPS) have been studied over a 10 year period and successfully applied at polycyclic hydrocarbon (PHC) contaminated sites, gas stations, and salt-contaminated sites throughout Canada. Soils are tilled in order to expose contaminants to sunlight. hydrocarbon-degrading bacteria are then applied, followed by the application of a plant growth promoting rhizobacteria (PGPR) phytoremediation system that is typically applied to grass species prior to planting. Case studies of full-scale sites used to prove the concept for both salt and hydrocarbon contaminated soils were presented. tabs., figs.

  19. Innovative tank emptying system for the retrieval of salt, sludge and IX resins from storage tanks of NPPs

    International Nuclear Information System (INIS)

    RWE NUKEM recently developed a new Tank Emptying System (TESY) for the extraction of stored radioactive boric acid/borate salt blocks, sludge and IX resin from NPP stainless steel tanks of several hundred cubic meters content in Russia. RWE NUKEM has chosen the emptying concept consisting of a tracked submersible vehicle ('Crawler'), with jet nozzles for solution, agitation and fluidization, and a suction head to pick up the generated solution or suspension respectively. With the employment of RWE NUKEM's TESY system, spent radioactive salt deposits, ion-exchange resins and sludge, can be emptied and transferred out of the tank. The sediment, crystallized and settled during storage, will be agitated with increased temperature and suitable pH value and then picked up in form of a suspension or solution directly at the point of mobilization. This new Tank Emptying System concept enables efficiently to retrieve stored salt and other sediment waste, reduces operating time, safes cost for spare parts, increases the safety of operation and minimizes radiation exposure to personnel. All emptying tasks are performed remotely from a panel board and TV monitor located in a central control room. The TESY system consists of the following main components: glove box, crawler, submersible pump, heater, TV camera and spot light, control panel and monitor, water separation and feed unit, sodium hydroxide dosing unit. The system is specially requested for the removal of more than 2,500 cubic meter salt solution generated from the dissolution of some 300 cubic meter crystallized salt deposit per tank and per year. The TESY system is able to dissolve efficiently the salts and retrieve solutions and other liquefied suspensions. TESY is adaptable to all liquid waste storage facilities and especially deployable for tanks with limited access openings (<550 mm)

  20. Design and In Vitro Evaluation of a New Nano-Microparticulate System for Enhanced Aqueous-Phase Solubility of Curcumin

    Directory of Open Access Journals (Sweden)

    Diana Guzman-Villanueva

    2013-01-01

    Full Text Available Curcumin, a yellow polyphenol derived from the turmeric Curcuma longa, has been associated with a diverse therapeutic potential including anti-inflammatory, antioxidant, antiviral, and anticancer properties. However, the poor aqueous solubility and low bioavailability of curcumin have limited its potential when administrated orally. In this study, curcumin was encapsulated in a series of novel nano-microparticulate systems developed to improve its aqueous solubility and stability. The nano-microparticulate systems are based entirely on biocompatible, biodegradable, and edible polymers including chitosan, alginate, and carrageenan. The particles were synthesized via ionotropic gelation. Encapsulating the curcumin into the hydrogel nanoparticles yielded a homogenous curcumin dispersion in aqueous solution compared to the free form of curcumin. Also, the in vitro release profile showed up to 95% release of curcumin from the developed nano-microparticulate systems after 9 hours in PBS at pH 7.4 when freeze-dried particles were used.

  1. Effects of a Pre-Filter and Electrolysis Systems on the Reuse of Brine in the Chinese Cabbage Salting Process

    OpenAIRE

    Kim, Dong-Ho; Yoo, Jae Yeol; Jang, Keum-Il

    2016-01-01

    In this study, the effects of a pre-filter system and electrolysis system on the safe and efficient reuse of brine in the cabbage salting process were investigated. First, sediment filter-electrolyzed brine (SF-EB) was selected as brine for reuse. Then, we evaluated the quality and microbiological properties of SF-EB and Chinese cabbage salted with SF-EB. The salinity (9.4%) and pH (4.63) of SF-EB were similar to those of control brine (CB). SF-EB turbidity was decreased (from 0.112 to 0.062)...

  2. Influence factors for the oxidation of pyrite by oxygen and birnessite in aqueous systems.

    Science.gov (United States)

    Qiu, Guohong; Luo, Yao; Chen, Cheng; Lv, Qiang; Tan, Wenfeng; Liu, Fan; Liu, Chengshuai

    2016-07-01

    The oxidation of exposed pyrite causes acid mine drainage, soil acidification, and the release of toxic metal ions. As the important abiotic oxidants in supergene environments, oxygen and manganese oxides participate in the oxidation of pyrite. In this work, the oxidation processes of natural pyrite by oxygen and birnessite were studied in simulated systems, and the influence of pH, Fe(II) and Cr(III) on the intermediates and redox rate was investigated. SO4(2-) and elemental S were formed as the major and minor products, respectively, during the oxidation processes. Ferric (hydr) oxides including Fe(OH)3 and goethite were formed with low degree of crystallinity. Low pH and long-term reaction facilitated the formation of goethite and ferric hydroxide, respectively. The rate of pyrite oxidation by birnessite was enhanced in the presence of air (oxygen), and Fe(II) ions played a key role in the redox process. The addition of Fe(II) ions to the reaction system significantly enhanced the oxidation rate of pyrite; however, the presence of Cr(III) ions remarkably decreased the pyrite oxidation rate in aqueous systems. The introduction of Fe(II) ions to form a Fe(III)/Fe(II) redox couple facilitated the electron transfer and accelerated the oxidation rate of pyrite. The present work suggests that isolation from air and decreasing the concentration of Fe(II) ions in aqueous solutions might be effective strategies to reduce the oxidation rate of pyrite in mining soils. PMID:27372130

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

    International Nuclear Information System (INIS)

    (Liquid + liquid) equilibrium (LLE) for the {poly ethylene glycol di-methyl ether 2000 (PEGDME2000) + Na2HPO4 + H2O} 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 - T0) 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 PEGDME2000 and poly ethylene glycol 2000 on phase forming ability were studied. The complete phase diagram for the poly ethylene {glycol di-methyl ether 2000 (PEGDME2000) + Na2HPO4 + H2O} system has also been determined at T = 298.15 K.

  4. Solubility and phase behavior of binary systems containing salts based on transitional metals

    International Nuclear Information System (INIS)

    Highlights: • Solubilities of salts were enhanced by temperature increase. • For all studied systems activity coefficients lower then unity were observed. • Melting point depression of 20 K was observed for [bmim]3[GdCl6]. -- Abstract: Tri(1-ethyl-3-methylimidazolium) gadolinium hexachloride ([emim]3[GdCl6]), tri(1-butyl-3-methylimidazolium) hexagadolinium chloride ([bmim]3[GdCl6]), di(tetramethylammonium) manganese tetrachloride ([TMA]2[MnCl4]) and cholinium tetrachloroferrate ([Chol][FeCl4]) were synthetized and their solubility in water, ethanol, 1-propanol and 1-butanol were determined as a function of temperature. Activity coefficients were calculated and their comparison with ideal solutions is discussed. The experimental data were correlated successfully by means of the semi-empirical Grant equation. In addition, melting point depression effect of high pressure carbon dioxide was studied

  5. Extraction-Chromogenic Systems Containing Iron(III, 4-(2-Thiazolylazoresorcinol and Ditetrazolium Salts

    Directory of Open Access Journals (Sweden)

    Kiril B. Gavazov

    2015-06-01

    Full Text Available Liquid-liquid extraction systems containing FeIII, 4-(2-thiazolylazoresorcinol (TAR, and a ditetrazolium salt (DTS: Neotetrazoliumchlortide, Blue Tetrazolium chloride, or Nitro Blue Tetrazolium chloride, water and chloroform were investigated. The optimum conditions for iron extraction, some equilibrium constants (association constants, distribution constants, and extraction constants, and characteristics (molar absorptivities, Sandell’s sensitivities, limits of detection and quantification were found. The extracted species are ternary complexes with a general formula of (DT2+[FeII(TAR2]. In this formula the metal ion is in oxidation state II, the azo dye is in doubly deprotonated form (TAR2−, and the ditetrazoliumcation (DT has a charge of 2+.

  6. Electrochemiluminescence of terbium (III)-two fluoroquinolones-sodium sulfite system in aqueous solution

    Science.gov (United States)

    Chen, Shi-lv; Ding, Fen; Liu, Yu; Zhao, Hui-chun

    2006-05-01

    The electrochemiluminescence (ECL) of Tb 3+-enoxacin-Na 2SO 3 system (ENX system) and Tb 3+-ofloxacin-Na 2SO 3 system (OFLX system) in aqueous solution is reported. ECL is generated by the oxidation of Na 2SO 3, which is enhanced by Tb 3+-fluoroquinolone (FQ) complex. The ECL intensity peak versus potential corresponds to oxidation of Na 2SO 3, and the ECL emission spectra (the peaks are at 490, 545, 585 and 620 nm) match the characteristic emission spectrum of Tb 3+, indicating that the emission is from the excited state of Tb 3+. The mechanism of ECL is proposed and the difference of ECL intensity between ENX system and OFLX system is explained. Conditions for ECL emission were optimized. The linear range of ECL intensity versus concentrations of pharmaceuticals is 2.0 × 10 -10-8.0 × 10 -7 mol l -1 for ENX and 6.0 × 10 -10-6.0 × 10 -7 mol l -1 for OFLX, respectively. A theoretical limit of detection is 5.4 × 10 -11 mol l -1 for ENX and 1.6 × 10 -10 mol l -1 for OFLX, respectively. The ECL was satisfactorily applied to the determination of the two FQs in dosage form and urine sample.

  7. Relationships between salt sensitivity of blood pressure and sympathetic nervous system activity: a short review of evidence.

    Science.gov (United States)

    Strazzullo, P; Barbato, A; Vuotto, P; Galletti, F

    2001-01-01

    Experimental and clinical studies provided evidence in favor of complex relationships between sympathetic nervous system activity and salt-sensitivity of blood pressure. Genetic and acquired metabolic alterations associated with a tendency to retain salt and water may generate salt-sensitivity of blood pressure and shift the pressure-natriuresis curve to the right, promoting an increase in blood pressure. Sympathetic activation is a factor contributing to this result. Chronic high dietary salt intake is followed by a derangement in mechanisms of central sympathetic inhibition and then by an enhanced peripheral sympathetic tone. This, in turn, may generate salt-sensitivity of blood pressure by affecting renal hemodynamics, tubular sodium and water handling. Insulin resistance and sodium and water retention are prompted by high-fat (as well as high carbohydrate) diets, and by an increase in body fat mass. Also, aging is a condition of impaired interactions of the above factors. A gain in weight due to reduced physical activity, not followed by a parallel decrease in calorie intake, brings to a fall in insulin sensitivity. In many cases, the natural age-related decline of renal function is associated with a reduced physical exercise, hyperinsulinemia and sodium retention; sympathetic nervous system activity is enhanced and causes an increase in blood pressure. PMID:11270585

  8. Characterization of adsorption of aqueous arsenite and arsenate onto charred dolomite in microcolumn systems.

    Science.gov (United States)

    Salameh, Yousef; Al-Muhtaseb, Ala'a H; Mousa, Hasan; Walker, Gavin M; Ahmad, Mohammad N M

    2014-01-01

    In this work, the removal of arsenite, As(III), and arsenate, As(V), from aqueous solutions onto thermally processed dolomite (charred dolomite) via microcolumn was evaluated. The effects of mass of adsorbent (0.5-2 g), initial arsenic concentration (50-2000 ppb) and particle size (dolomite in a microcolumn were investigated. It was found that the adsorption of As(V) and As(III) onto charred dolomite exhibited a characteristic 'S' shape. The adsorption capacity increased as the initial arsenic concentration increased. A slow decrease in the column adsorption capacity was noted as the particle size increased from>0.335 to 0.710-2.00 mm. For the binary system, the experimental data show that the adsorption of As(V) and As(III) was independent of both ions in solution. The experimental data obtained from the adsorption process were successfully correlated with the Thomas Model and Bed Depth Service Time Model. PMID:25244130

  9. Removal of uranium from drinking water and other aqueous systems using modified powdered activated carbon

    International Nuclear Information System (INIS)

    A simple, rapid and eco friendly method for removal of high concentration of Uranium (U) from ground water (>2500 ppb), Mine water(>1000 ppb) and other aqueous systems has been developed based on laboratory trials using 10 litres of mine water and ground water. The removal of uranium was greater than 95% with a contact time of 10 minutes with modified powdered activated carbon (MPAC) at the natural pH of water. The concentration of Uranium left behind in drinking water after MPAC treatment (if necessary twice) was less than 15 ppb and is below WHO/AERB permissible limits. The methodology is so simple that it could be applied at remote villages to produce uranium free drinking water at the natural pH of water

  10. Table 5.1. Exchange current densities and rate constants in aqueous systems

    Science.gov (United States)

    Holze, R.

    This document is part of Volume 9 `Electrochemistry', Subvolume A, of Landolt-Börnstein - Group IV `Physical Chemistry'. This document lists the exchange current densities and the electrode reaction rate constants of the following metallic electrodes in aqueous systems for various electrolyte reactions: silver (Ag), aluminium (Al), gold (Au), bismuth (Bi), carbon (C), cadmium (Cd), cobalt (Co), chromium (Cr), cesium (Cs), copper (Cu), iron (Fe), gallium (Ga), mercury (Hg), indium (In), iridium (Ir), potassium (K), lithium (Li), molybdenum (Mo), natrium (Na), niobium (Nb), nickel (Ni), lead (Pb), palladium (Pd), platinum (Pt), rubidium (Rb), rhodium (Rh), ruthenium (Ru), antimony (Sb), tin (Sn), tantalum (Ta), titanium (Ti), thallium (Tl), vanadium (V), tungsten (W), zinc (Zn). For each electrolyte reaction the electrolyte solution, the educt, product and concentration are specified along with the temperature of determination of the given values.

  11. Novel synthetic approach for 1, 4-dihydroxyanthraquinone and the development of its Lithiated salts as anode material for aqueous rechargeable Lithium-ion batteries

    KAUST Repository

    Gurukar, Suresh Shivappa

    2015-08-17

    The influence of organic electrode materials in the field of lithium ion battery is becoming a keen interest for the present generation scientists. Here we are reporting a novel method of synthesis of electrode material by the combination of sono-chemical and thermal methods. The advantages of organic active material towards lithium ion battery are of core interest of this study. The structural confirmations are by FT-IR, 1H NMR, MALDI-TOF Mass Spectroscopy and powder XRD data. The electrochemical properties of Lithiated-1,4-dihydroxyanthraquinone were studied using electrochemical-techniques such as Cyclic Voltammetry, Galvanostatic Cyclic Potential Limitation and Potentiostatic Electrochemical Impedance Spectroscopy. The satisfactory results towards stability of active species in the aqueous media, reasonable discharge capacity with 0.9 V average voltages and agreeable cycling performance during charge-discharge process with reproducibility are achieved. For the construction of the full cell, the anode material was coupled with the LiNi1/3Co1/3Mn1/3O2 as a cathode material.

  12. Potential of salt-accumulating and salt-secreting halophytic plants for recycling sodium chloride in human urine in bioregenerative life support systems

    Science.gov (United States)

    Tikhomirova, N. A.; Ushakova, S. A.; Kudenko, Yu. A.; Gribovskaya, I. V.; Shklavtsova, E. S.; Balnokin, Yu. V.; Popova, L. G.; Myasoedov, N. A.; Gros, J.-B.; Lasseur, Ch.

    2011-07-01

    This study addresses the possibility of growing different halophytic plants on mineralized human urine as a way to recycle NaCl from human wastes in a bioregenerative life support system (BLSS). Two halophytic plant species were studied: the salt-accumulating Salicornia europaea and the salt-secreting Limonium gmelinii. During the first two weeks, plants were grown on Knop's solution, then an average daily amount of urine produced by one human, which had been preliminarily mineralized, was gradually added to the experimental solutions. Nutrient solutions simulating urine mineral composition were gradually added to control solutions. NaCl concentrations in the stock solutions added to the experimental and control solutions were 9 g/L in the first treatment and 20 g/L in the second treatment. The mineralized human urine showed some inhibitory effects on S. europaea and L. gmelinii. The biomass yield of experimental plants was lower than that of control ones. If calculated for the same time period (120 d) and area (1 m 2), the amount of sodium chloride taken up by S. europaea plants would be 11.7 times larger than the amount taken up by L. gmelinii plants (486 g/m 2 vs. 41 g/m 2). Thus, S. europaea is the better choice of halophyte for recycling sodium chloride from human wastes in BLSS.

  13. Basin Analysis and Petroleum System Characterization and Modeling, Interior Salt Basins, Central and Eastern Gulf of Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Ernest A. Mancini; Paul Aharon; Donald A. Goddard; Roger Barnaby

    2006-05-26

    The principal research effort for Phase 1 (Concept Development) of the project has been data compilation; determination of the tectonic, depositional, burial, and thermal maturation histories of the North Louisiana Salt Basin; basin modeling (geohistory, thermal maturation, hydrocarbon expulsion); petroleum system identification; comparative basin evaluation; and resource assessment. Existing information on the North Louisiana Salt Basin has been evaluated, an electronic database has been developed, and regional cross sections have been prepared. Structure, isopach and formation lithology maps have been constructed, and burial history, thermal maturation history, and hydrocarbon expulsion profiles have been prepared. Seismic data, cross sections, subsurface maps and burial history, thermal maturation history, and hydrocarbon expulsion profiles have been used in evaluating the tectonic, depositional, burial and thermal maturation histories of the basin. Oil and gas reservoirs have been found to be associated with salt-supported anticlinal and domal features (salt pillows, turtle structures and piercement domes); with normal faulting associated with the northern basin margin and listric down-to-the-basin faults (state-line fault complex) and faulted salt features; and with combination structural and stratigraphic features (Sabine and Monroe Uplifts) and monoclinal features with lithologic variations. Petroleum reservoirs include Upper Jurassic and Cretaceous fluvial-deltaic sandstone facies; shoreline, marine bar and shallow shelf sandstone facies; and carbonate shoal, shelf and reef facies. Cretaceous unconformities significantly contribute to the hydrocarbon trapping mechanism capacity in the North Louisiana Salt Basin. The chief petroleum source rock in this basin is Upper Jurassic Smackover lime mudstone beds. The generation of hydrocarbons from Smackover lime mudstone was initiated during the Early Cretaceous and continued into the Tertiary. Hydrocarbon

  14. A method for separating water soluble organics from a process stream by aqueous biphasic extraction

    Energy Technology Data Exchange (ETDEWEB)

    Chaiko, David J.; Mego, William A.

    1997-12-01

    The present invention relates to a method for separating water-miscible organic species from a process stream by aqueous biphasic extraction. In particular, the method includes extracting the organic species into a polymer-rich phase of an aqueous biphase system in which the process stream comprises the salt-rich phase, and, next, separating the polymer from the extracted organic species by contacting the loaded, polymer-rich phase with a water-immiscible organic phase. Alternatively, the polymer can be separated from the extracted organic species by raising the temperature of the loaded, polymer-rich phase above the cloud point, such that the polymer and the water-soluble organic species separate into two distinct aqueous phases. In either case, a substantially salt-free, concentrated aqueous solution containing the organic species is recovered.

  15. Reversal of cardiac fibrosis in deoxycorticosterone acetate-salt hypertensive rats by inhibition of the renin-angiotensin system.

    Science.gov (United States)

    Brown, L; Duce, B; Miric, G; Sernia, C

    1999-01-01

    Fibrosis impairs cardiac function. This project has determined the expression and deposition of collagens and fibronectin and cardiac function in the deoxycorticosterone acetate (DOCA)-salt hypertensive rat after inhibition of the renin-angiotensin system. DOCA-salt hypertension was induced in 8-wk-old male Wistar rats by uninephrectomy and administration of DOCA (25 mg every fourth day, subcutaneously) and 1% NaCl in the drinking water for 4 wk. Starting 2 wk after surgery, rats were given either oral captopril (100 mg/kg), oral candesartan cilexetil (2 mg/kg), or subcutaneous spironolactone (50 mg/kg) daily for 2 wk (reversal protocol). DOCA-salt rats failed to gain weight with markedly increased water intake and decreased food intake; drug treatment did not alter these parameters. Systolic BP increased from 116+/-5 mmHg in uninephrectomized rats to 179+/-7 mmHg in DOCA-salt rats and was not decreased by treatment (captopril 172+/-1 mmHg; candesartan 187+/-2 mmHg; spironolactone 178+/-3 mmHg). Captopril, candesartan, and spironolactone reversed the increased collagen I mRNA in DOCA-salt rats; only candesartan reversed the increased collagen III mRNA. Collagen IV mRNA was unchanged in DOCA-salt rats and following treatment. Total fibronectin mRNA increased without changing the proportion of fibronectin mRNA as the fetal isoforms EIIIA and EIIIB. Captopril, candesartan, and spironolactone reversed the increased deposition of perivascular and interstitial collagen in DOCA-salt rats; the increased cardiac fibronectin deposition was reversed by candesartan and spironolactone. Captopril, candesartan, and spironolactone also attenuated or reversed the increased diastolic stiffness and the increased dP/dt but not the increased rate-pressure products in DOCA-salt rat hearts. Thus, inhibition of the renin-angiotensin system reverses cardiac fibrosis in DOCA-salt rats and returns some indices of myocardial function to normal. PMID:9892155

  16. Combine Studies Pertaining to the Solubility of Neptunium in Oxidizing Aqueous Systems

    International Nuclear Information System (INIS)

    The report combines two separate studies dealing with different aspects of the behavior of neptunium in oxidizing aqueous systems. The goal of both studies is to obtain a better understanding of what would control the concentration of neptunium in oxidizing groundwaters upon release from a geologic high-level waste repository. 237Np has a very long half-life, and consequently tends to appear as a component of concern in long-term dose calculations. Part A examines the formation of NpO2 [Np(IV) oxide] from aqueous Np(V) under oxidizing conditions, using elevated temperature as a means of accelerating putative slow kinetics. According to thermodynamic data, NpO2 should be the stable Np solid, even though Np is generally thought to be mainly some form of Np(V) under oxidizing conditions. The first observed precipitation of this solid from aqueous solution under any conditions is reported. This result suggests, but does not prove, that long-term very slow formation of NpO2 might be an important long-term control on neptunium migration. Even at 200oC, the kinetics can be sluggish on typical experimental time scales. Though not reported in Part A, a similar situation may exist for Pu, and NpO2 and PuO2 may potentially form solid solutions. Under reducing conditions, UO2 might join in. Part B examines the interaction of Np(V) with the uranium mineral schoepite. Is neptunium incorporated into the crystal structure as a solid-solution component, or does it just sorb onto the mineral surface? The results presented here suggest that it basically just sorbs onto the surface, which would be a less effective process in limiting neptunium migration. This is not a surprising result, as schoepite is a relatively simple solid of U(VI). There is no obvious means to compensate for the charge difference between U(VI) and Np(V) without introducing unfavorable energetics. However, the results reported here do not rule out a possible substitution of Np(VI) in schoepite or other U

  17. Effects of organic solvents on the partitioning of enzymes in aqueous two-phase systems.

    Science.gov (United States)

    Johansson, G; Kopperschläger, G

    1987-02-13

    Organic solvents (ethylene glycol, glycerol, dimethyl sulphoxide, dimethylformamide, dioxane, methanol and propanol-2, as well as sucrose and urea) have been included in aqueous two-phase (liquid-liquid) systems comprised of water, dextran and poly(ethylene glycol). The concentration of the organic solvent was in most cases 20% (w/w). The influence of these solvents on the phase-forming properties, the volume ratio, the freezing point and the partitioning of a polymer-bound ligand, Procion Red HE-3B poly(ethylene glycol), has been studied. The partition coefficients for alkaline phosphatase decrease with ethylene glycol, glycerol, sucrose and urea (factors of 0.25-0.5), but increase with the other substances (factors of 1.2-1.6). The temperature effects on the partitioning of alkaline phosphatase from calf intestine as well as of phosphofructokinase from yeast in systems containing ethylene glycol have been studied and compared with partitioning in standard systems, not containing solvents. The possible uses of the above systems for partitioning studies of enzymes are discussed. PMID:2951391

  18. Utilization of the Donnan potential induced by reverse salt flux in pressure retarded osmosis systems.

    Science.gov (United States)

    Park, Chul Ho; Kwak, Sung Jo; Nam, Joo-Youn; Jang, Moon Seok; Lee, Jung-Hyun

    2016-09-14

    Pressure retarded osmosis (PRO) generates energy from salinity gradients. Reverse salt flux through a semi-permeable PRO membrane reduces the energy efficiency. We demonstrate for the first time the direct conversion of the reverse salt flux into electrochemical potential, recovering >7% positive net power using a single electrochemical PRO membrane. PMID:27523633

  19. Influence of abiotic factors on spider and ground beetle communities in different salt-marsh systems

    NARCIS (Netherlands)

    Petillon, Julien; Georges, Anita; Canard, Alain; Lefeuvre, Jean-Claude; Bakker, Jan P.; Ysnel, Frederic

    2008-01-01

    Salt marshes are interesting and endangered ecosystems in West-Europe. Nevertheless, their arthropod fauna remains largely unknown and the factors determining assemblages at micro-habitat scale are poorly understood. Few data are also available about the effects of management measures in salt marshe

  20. N-Arylation of amines, amides, imides and sulfonamides with arylboroxines catalyzed by simple copper salt/EtOH system

    OpenAIRE

    Zheng, Zhang-Guo; Wen, Jun; Wang, Na; Wu, Bo; Yu, Xiao-Qi

    2008-01-01

    The coupling of arylboroxines with a variety of amines, amides, imides and sulfonamides catalyzed by a copper salt/EtOH system has been developed. In the absence of a base or additive the corresponding N-arylation products were obtained in moderate to excellent yields.

  1. Rapid synthesis of zeolitic imidazolate framework-8 (ZIF-8) nanocrystals in an aqueous system

    KAUST Repository

    Pan, Yichang

    2011-01-01

    We report here the first example of ZIF materials synthesized in aqueous solution. The synthesis was performed at room temperature and typically took several minutes compared to hours and days in non-aqueous conditions. The obtained product were ZIF-8 nanocrystals having size of ∼85 nm and showed excellent thermal, hydrothermal and solvothermal stabilities. © 2011 The Royal Society of Chemistry.

  2. BASIN ANALYSIS AND PETROLEUM SYSTEM CHARACTERIZATION AND MODELING, INTERIOR SALT BASINS, CENTRAL AND EASTERN GULF OF MEXICO

    Energy Technology Data Exchange (ETDEWEB)

    Ernest A. Mancini; Donald A. Goddard; Ronald K. Zimmerman

    2005-05-10

    The principal research effort for Year 2 of the project has been data compilation and the determination of the burial and thermal maturation histories of the North Louisiana Salt Basin and basin modeling and petroleum system identification. In the first nine (9) months of Year 2, the research focus was on the determination of the burial and thermal maturation histories, and during the remainder of the year the emphasis has basin modeling and petroleum system identification. Existing information on the North Louisiana Salt Basin has been evaluated, an electronic database has been developed, regional cross sections have been prepared, structure and isopach maps have been constructed, and burial history, thermal maturation history and hydrocarbon expulsion profiles have been prepared. Seismic data, cross sections, subsurface maps and related profiles have been used in evaluating the tectonic, depositional, burial and thermal maturation histories of the basin. Oil and gas reservoirs have been found to be associated with salt-supported anticlinal and domal features (salt pillows, turtle structures and piercement domes); with normal faulting associated with the northern basin margin and listric down-to-the-basin faults (state-line fault complex) and faulted salt features; and with combination structural and stratigraphic features (Sabine and Monroe Uplifts) and monoclinal features with lithologic variations. Petroleum reservoirs are mainly Upper Jurassic and Lower Cretaceous fluvial-deltaic sandstone facies and Lower Cretaceous and Upper Cretaceous shoreline, marine bar and shallow shelf sandstone facies. Cretaceous unconformities significantly contribute to the hydrocarbon trapping mechanism capacity in the North Louisiana Salt Basin. The chief petroleum source rock in this basin is Upper Jurassic Smackover lime mudstone beds. The generation of hydrocarbons from Smackover lime mudstone was initiated during the Early Cretaceous and continued into the Tertiary

  3. Heterogeneous equilibria in the Mm(BUO5)m · nH2O-aqueous HCl system

    International Nuclear Information System (INIS)

    Solubility of crystal uranoborate of alkali and alkaline-earth metals of the composition Mm(BUO5)m · nH2O (Mm = Li-Cs, Mg-Ba) in HCl aqueous solutions 10-4-10-1 M at 25 deg C was studied. Relying on the experimental data obtained, a quantitative model of the aqueous system was suggested and physicochemical description of the uranoborates state in solutions was given. Using the method of equilibrium thermodynamics, the standard thermodynamic functions of the compounds studied were ascertained

  4. Approach to the extreme safety in a nuclear fuel reprocessing system in mild aqueous solutions

    International Nuclear Information System (INIS)

    The purpose of the experiment is to establish a new nuclear fuel reprocessing system, which is aimed to achieve the extreme safety. In order to avoid any potential danger of explosion, all processes are made by the precipitation method at room temperature. The system consists of the following processes: 1. crystallization of uranyl nitrate from a dissolved fuel solution by cooling the solution; 2. complex formation of UO22+ and Pu4+ with carbonate ion by the addition of Na2CO3-NaHCO3 solution adjusting pH to 9, followed by the separation of a precipitate containing the major fission products by the centrifugation method; 3. separation of Cs as a precipitate of cesium tetraphenylborate; 4. recovery of U and Pu as precipitates of hydroxo compounds from the alkaline solution by the addition of NaOH solution ; 5. separation of Sr from the precipitate in process 2; 6. recovery of NaHCO3 from the NaOH solution by bubbling CO2 gas. As a result, 99.95% of the U was recovered with the least amount of fission products. Pu are expected to be recovered in the same way as U. In conclusion, the present reprocessing system enables us to recover U and Pu in high ratios from spent nuclear fuel by means of a simple precipitation method, to separate hazardous Cs and Sr from high-level waste, and to exclude any potential danger owing to chemical processes under mild aqueous conditions. (author)

  5. Investigation of radioprotective effects of aqueous extract of sauseurea obyallata on immune system of mice

    International Nuclear Information System (INIS)

    Objective: To investigate the radioprotective effects of test compound on immune system of mice from radiation injury. Methods: Immunologic function and general state of mice were shown by swimming experiment with the weighing of spleen, thymus and computing their indexs, hemolysin mensurate experiment and PHA stimulated lymphocyte transformation experiment. All mice were irradiated with 6 Gy and received the test compound by gavage for 14 days, 7 days before irradiation and 7 days after irradiation. All the indicators were measured according to established methods. The data went through Statistical analysis by spss11.5. Results: Irradiation has obvious influence on the immune function and systemic state of mice. In swimming experiment, mice in the treatment group swim longer than the model group, but is of no significant difference. The thymus indexes are higher in treatment groups than in model group, especially the HD group, compared with model group, the differences are obvious (P<0.05). There is no obvious difference between treatment groups and model group with OD value in hemolysin mensurate experiment. Conclusions: Aqueous Extract of Sauseurea Obyallata may have radioprotective effects on immune system of mice, which deserves further exploration in the compound preparing, analysis of Chemical Compositions and the dose and mode and the treatment duration of the compound. (authors)

  6. Nucleation and capture of condensible airborne contaminants in an aqueous scrubbing system

    International Nuclear Information System (INIS)

    The fate of condensible contaminants in an aqueous scrubbing system was evaluated. Knowledge of the behavior of volatile fission product compounds is important in evaluating the effectiveness of emergency air cleaning systems proposed for use in containment systems of breeder reactor plants. When a high temperature air stream passes through a spray quench chamber, very large cooling rates occur in the drop boundary layers. These large cooling rates cause large supersaturations in airborne concentrations of condensible contaminants, and one predicts that most condensation would take place through homogeneous nucleation. The very small particles formed would agglomerate, and attach to sodium aerosol particles which would be present. In the study the overall removal efficiency of volatile fission product species (typified by NaI, SeO2, and Sb2O3) in an air cleaning train (quench chamber, venturi scrubber, and fibrous bed) was theoretically evaluated. The overall removal efficiency of condensible materials was found to be lower than that for sodium compound aerosols because the freshly condensed particles would be smaller in size. For a base case, a removal efficiency of 99.97 percent was predicted for condensible materials. The fibrous bed scrubber exhibited superior particle removal characteristics for small particles compared to the quench chamber and venturi scrubber. Its removal efficiency exceeded 97 percent for even the most penetrating particle size (about 0.4 micron aerodynamic diameter). Therefore, all condensible fission products would be removed with efficiencies exceeding 97 percent

  7. Microbial side-chain cleavage of phytosterols by mycobacteria in vegetable oil/aqueous two-phase system.

    Science.gov (United States)

    Xu, Yang-Guang; Guan, Yi-Xin; Wang, Hai-Qing; Yao, Shan-Jing

    2014-09-01

    Microbial side-chain cleavage of natural sterols to 4-androstene-3,17-dione (AD) and 1,4-androstadiene-3,17-dione (ADD) by Mycobacteria has received much attention in pharmaceutical industry, while low yield of the reaction owing to the strong hydrophobicity of sterols is a tough problem to be solved urgently. Eight kinds of vegetable oils, i.e., sunflower, peanut, corn, olive, linseed, walnut, grape seed, and rice oil, were used to construct oil/aqueous biphasic systems in the biotransformation of phytosterols by Mycobacterium sp. MB 3683 cells. The results indicated that vegetable oils are suitable for phytosterol biotransformation. Specially, the yield of AD carried out in sunflower biphasic system (phase ratio of 1:9, oil to aqueous) was greatly increased to 84.8 % with 10 g/L feeding concentration after 120-h transformation at 30 °C and 200 rpm. Distribution coefficients of AD in different oil/aqueous systems were also determined. Because vegetable oils are of low cost and because of their eco-friendly characters, there is a great potential for the application of oil/aqueous two-phase systems in bacteria whole cell biocatalysis. PMID:25082765

  8. 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.

  9. 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...

  10. Poly(3-hydroxybutyrate) and Eudragit E microparticles: a release system to enhance the aqueous solubility of felodipine and simvastatin

    International Nuclear Information System (INIS)

    Poor water-soluble drugs are a problem for the development of oral solid dosage forms, since it has great potential for low bioavailability. Thus, release systems that promote the increase of aqueous solubility of these drugs are advantageous. This study aimed to evaluate the feasibility of incorporation of felodipine and simvastatin in polymeric microparticles, to improve the aqueous solubility of the drugs. Microparticles of poly(3-hydroxybutyrate) [PHB] and Eudragit E was prepared by emulsion - solvent evaporation technique and characterized as to morphology and encapsulation efficiency of the drugs. Particles with spherical shapes and high levels of drug encapsulated were obtained. There was a significant increase in aqueous solubility of felodipine and simvastatin after its incorporation into the polymeric microparticles. X-ray diffraction analysis showed the conversion of both drugs to amorphous form, which may have contributed to increased the solubility. (author)

  11. Magneto-hydrodynamic detection of vortex shedding for molten salt flow sensing.

    Energy Technology Data Exchange (ETDEWEB)

    Kruizenga, Alan Michael; Crocker, Robert W.

    2012-09-01

    High temperature flow sensors must be developed for use with molten salts systems at temperatures in excess of 600%C2%B0C. A novel magneto-hydrodynamic sensing approach was investigated. A prototype sensor was developed and tested in an aqueous sodium chloride solution as a surrogate for molten salt. Despite that the electrical conductivity was a factor of three less than molten salts, it was found that the electrical conductivity of an electrolyte was too low to adequately resolve the signal amidst surrounding noise. This sensor concept is expected to work well with any liquid metal application, as the generated magnetic field scales proportionately with electrical conductivity.

  12. Extraction protease expressed by Penicillium fellutanum from the Brazilian savanna using poly(ethylene glycol)/sodium polyacrylate/NaCl aqueous two-phase system.

    Science.gov (United States)

    Barros, Kleber V G; Souza, Paula M; Cardoso, Samuel L; Borges, Leonardo L; Filho, Edivaldo X F; Junior, Adalberto P; Magalhães, Pérola O

    2015-01-01

    The partitioning of protease expressed by Penicillium fellutanum from the Brazilian savanna in a novel inexpensive and stable aqueous two-phase system (ATPS) composed of poly(ethylene glycol) (PEG) and sodium polyacrylate (NaPA) was studied in this work using factorial design. The ATPS is formed by mixing both polymers with a salt (NaCl) and fermented broth of P. fellutanum. The effects of molar mass (2,000, 4,000, and 6,000 g ⋅ mol(-1)) and concentration (6, 8, and 10 wt%) of PEG and that of NaPA concentration (6, 8, and 10 wt%) on protease partitioning (K) at 25 °C were studied. A two-level factorial design (2(3)) was implemented. The effect of Na2 SO4 concentration (5, 10, and 15 wt%) on the reextraction of the enzyme was also analyzed. The partition coefficient K ranged from 77.51 to 1.21, indicating the versatility of the method. The reextraction was achieved with the addition of 5% Na2 SO4 , allowing the partitioning of the protease to the upper phase, whereas total proteins were directed to the bottom phase. The results of partitioning using the PEG/NaPA/NaCl system and that of the subsequent reextraction with Na2 SO4 suggest that this method can be used to purify proteases from fermented broth of P. fellutanum. PMID:25546578

  13. Heat Transfer Salts for Nuclear Reactor Systems - Chemistry Control, Corrosion Mitigation, and Modeling

    International Nuclear Information System (INIS)

    The concept of a molten salt reactor has existed for nearly sixty years. Previously all work was done during a large collaborative effort at Oak Ridge National Laboratory, culminating in a research reactor which operated for 15,000 hours without major error. This technical success has garnished interest in modern, high temperature, reactor schemes. Research using molten fluoride salts for nuclear applications requires a steady supply of high grade molten salts. There is no bulk supplier of research grade fluoride salts in the world, so a facility which could provide all the salt needed for testing at the University of Wisconsin had to be produced. Two salt purification devices were made for this purpose, a large scale purifier, and a small scale purifier, each designed to clean the salts from impurities and reduce their corrosion potential. As of now, the small scale has performed with flibe salt, hydrogen, and hydrogen fluoride, yielding clean salt. This salt is currently being used in corrosion testing facilities at the Massachusetts Institute of Technology and the University of Wisconsin. Working with the beryllium based salts requires extensive safety measures and health monitoring to prevent the development of acute or chronic beryllium disease, two pulmonary diseases created by an allergic reaction to beryllium in the lungs. Extensive health monitoring, engineering controls, and environment monitoring had to be set up with the University of Wisconsin department of Environment, Health and Safety. The hydrogen fluoride required for purification was also an extreme health hazard requiring thoughtful planning and execution. These dangers have made research a slow and tedious process. Simple processes, such as chemical handling and clean-up, can take large amounts of ingenuity and time. Other work has complemented the experimental research at Wisconsin to advance high temperature reactor goals. Modeling work has been performed in house to re

  14. Heat Transfer Salts for Nuclear Reactor Systems - Chemistry Control, Corrosion Mitigation, and Modeling

    Energy Technology Data Exchange (ETDEWEB)

    Anderson, Mark; Sridharan, Kumar; Morgan, Dane; Peterson, Per; Calderoni, Pattrick; Scheele, Randall; Casekka, Andrew; McNamara, Bruce

    2015-01-22

    The concept of a molten salt reactor has existed for nearly sixty years. Previously all work was done during a large collaborative effort at Oak Ridge National Laboratory, culminating in a research reactor which operated for 15,000 hours without major error. This technical success has garnished interest in modern, high temperature, reactor schemes. Research using molten fluoride salts for nuclear applications requires a steady supply of high grade molten salts. There is no bulk supplier of research grade fluoride salts in the world, so a facility which could provide all the salt needed for testing at the University of Wisconsin had to be produced. Two salt purification devices were made for this purpose, a large scale purifier, and a small scale purifier, each designed to clean the salts from impurities and reduce their corrosion potential. As of now, the small scale has performed with flibe salt, hydrogen, and hydrogen fluoride, yielding clean salt. This salt is currently being used in corrosion testing facilities at the Massachusetts Institute of Technology and the University of Wisconsin. Working with the beryllium based salts requires extensive safety measures and health monitoring to prevent the development of acute or chronic beryllium disease, two pulmonary diseases created by an allergic reaction to beryllium in the lungs. Extensive health monitoring, engineering controls, and environment monitoring had to be set up with the University of Wisconsin department of Environment, Health and Safety. The hydrogen fluoride required for purification was also an extreme health hazard requiring thoughtful planning and execution. These dangers have made research a slow and tedious process. Simple processes, such as chemical handling and clean-up, can take large amounts of ingenuity and time. Other work has complemented the experimental research at Wisconsin to advance high temperature reactor goals. Modeling work has been performed in house to re

  15. Partition of Chiral pharmaceutical intermediate R(-)-Mandelic Acid in Aqueous Two-Phase System of Poly(ethylene glycol)-Ammonium Sulfate

    Institute of Scientific and Technical Information of China (English)

    Xu Xiaoping; Li Zhongqin; Chen Jiebo; Huang Xinghua

    2004-01-01

    An aqueous two-phase system of poly (ethylene glycol)-ammonium sulfate was employed to separate R (-)-mandelic acid.The result showed that R (-)-mandelic acid has priority to partition in PEG-rich top phase. This indicated that aqueous two-phase is a very suitable system for separation of R(-)-mandelic acid.

  16. CONTROLLING THE AQUEOUS MISCIBILITY OF IONIC LIQUIDS: A NOVEL AQUEOUS BIPHASIC SYSTEM FROM WATER-MISCIBLE IONIC LIQUID AND A WATER-STRUCTURING SALT. (R828257)

    Science.gov (United States)

    The perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Concl...

  17. Effect of salt stress on growth and physiology in amaranth and lettuce: Implications for bioregenerative life support system

    Science.gov (United States)

    Qin, Lifeng; Guo, Shuangsheng; Ai, Weidang; Tang, Yongkang; Cheng, Quanyong; Chen, Guang

    2013-02-01

    Growing plants can be used to clean waste water in bioregenerative life support system (BLSS). However, NaCl contained in the human urine always restricts plant growth and further reduces the degree of mass cycle closure of the system (i.e. salt stress). This work determined the effect of NaCl stress on physiological characteristics of plants for the life support system. Amaranth (Amaranthus tricolor L. var. Huahong) and leaf lettuce (Lactuca sativa L. var. Luoma) were cultivated at nutrient solutions with different NaCl contents (0, 1000, 5000 and 10,000 ppm, respectively) for 10 to 18 days after planted in the Controlled Ecological Life Support System Experimental Facility in China. Results showed that the two plants have different responses to the salt stress. The amaranth showed higher salt-tolerance with NaCl stress. If NaCl content in the solution is below 5000 ppm, the salt stress effect is insignificant on above-ground biomass output, leaf photosynthesis rate, Fv/Fm, photosynthesis pigment contents, activities of antioxidant enzymes, and inducing lipid peroxidation. On the other hand, the lettuce is sensitive to NaCl which significantly decreases those indices of growth and physiology. Notably, the lettuce remains high productivity of edible biomass in low NaCl stress, although its salt-tolerant limitation is lower than amaranth. Therefore, we recommended that amaranth could be cultivated under a higher NaCl stress condition (lettuce should be under a lower NaCl stress (<1000 ppm) for water cleaning in future BLSS.

  18. Membraneless dialysis of strontium in aqueous liquid-liquid milk-pectin system

    International Nuclear Information System (INIS)

    Binding of added strontium by milk proteins under native conditions was investigated using pectin of various degrees of esterification. The partition of strontium, as well as cesium and europium, in aqueous two-phase milk-pectin system, is discussed in terms of 'membraneless dialysis' and described by Donnan equilibria, and compared with the distribution between cation exchanger and milk, artificial milk serum, or pectin solutions. When going from pectin with a degree of esterification D.E. = 93.2 to 61.4, the distribution of strontium decreases for about 40% in favor of pectin phase and this was explained by a relatively lower degree of dissociation of free carboxyle groups of pectin. The low-molecular fraction of added strontium in milk was assessed from Dowex 50*8 sorption data to be 31%, and that of cesium and europium 58% and 40%, respectively. However, distribution ratio of strontium and europium in milk/pectin system is much higher than it would correspond to the ion exchanger adsorption data. (author) 16 refs.; 2 tabs

  19. Partition of volatile compounds in pea globulin-maltodextrin aqueous two-phase system.

    Science.gov (United States)

    Nguyen, Thanh Dat; Lafarge, Céline; Murat, Chloé; Mession, Jean-Luc; Cayot, Nathalie; Saurel, Rémi

    2014-12-01

    This study is based on the assumption that the off-flavour of pea proteins might be decreased using the retention of volatile compounds by a mixture with another biopolymer. The partition of volatile compounds in an aqueous system containing pea protein and maltodextrins was followed under thermodynamic incompatibility conditions. Firstly, the phase diagram of the system was established. Then, the partition of aroma compounds between the phase rich in protein and the phase rich in maltodextrin was measured by SPME-GC-MS. There was a transfer of volatile compounds during phase separation. Variations of pH were also used to vary the retention of volatile compounds by proteins. The concentration of volatile compounds in protein solution at pH 2.4 was higher than at pH 7.2. It was possible to increase the transfer of volatile compounds from the phase rich in protein to the phase rich in maltodextrin using the effect of pH on protein denaturation. PMID:24996351

  20. Hydrate phase equilibria of CO2+N2+aqueous solution of THF, TBAB or TBAF system

    DEFF Research Database (Denmark)

    Sfaxi, Imen Ben Attouche; Durand, Isabelle; Lugo, Rafael;

    2014-01-01

    We report hydrate dissociation conditions of CO2 (15 and 30mol%)+N2 (85 and 70mol%) in the presence of aqueous solutions of THF, TBAB or TBAF. The concentrations of TBAB and TBAF in the aqueous solutions are 5wt% and 9wt% while THF concentration in aqueous solution is 3mol%. Two different...... experimental techniques including isochoric pressure search method and a DSC method are used to measure the hydrate dissociation conditions. A comparison is finally made with the literature data. It is expected that this study provides better understanding of hydrate phase equilibria associated with CO2...... capture. © 2014 Elsevier Ltd....

  1. Simultaneous removal of organic matter and salt ions from saline wastewater in bioelectrochemical systems

    KAUST Repository

    Kim, Younggy

    2013-01-01

    A new bioelectrochemical system is proposed for simultaneous removal of salinity and organic matter. In this process, exoelectrogenic microorganisms oxidize organic matter and transfer electrons to the anode, hydrogen is evolved at the cathode by supplying additional voltage, and salt is removed from the wastewater due to the electric potential generated and the use of two ion-exchange membranes. Salinity removal (initial conductivity ~40mS/cm) increased from 21 to 84% by increasing the substrate (sodium acetate) from 2 to 8g/L. A total of 72-94% of the chemical oxygen demand was degraded in the anode and cathode chambers, with 1-4% left in the anode chamber and the balance lost through the anion-exchange membrane into the concentrate waste chamber. The maximum hydrogen production rate was 3.6m3-H2/m3-electrolyte per day at an applied potential of 1.2V. The Coulombic efficiency was ~100%, while the cathode recovery varied from 57 to 100%, depending on the extent of methanogenesis. Exoelectrogenic microbes generated high current densities (7.8mA/cm2) at ≤36g/L of total dissolved solids, but >41g/L eliminated current. These results provide a new method for achieving simultaneous removal of salinity and organic matter from a saline wastewater with H2 production. © 2012 Elsevier B.V.

  2. The anti-supercooling effect of surface-modified nano-scaled SiO2 in hydrated salts phase transition system

    International Nuclear Information System (INIS)

    Phase change characteristics of hydrate salt were analyzed for a system consisting of three types of SiO2 nano-particles doped phase change materials (PCMs). By using the three nano-particles of Aerosol SiO2, RNS-A SiO2 and Liquid phase SiO2, the surface effect of the interaction between nano-particles and hydrate salts was investigated. The time-temperature curves and Differential Scanning Calorimeter (DSC) testing results showed that Aerosol SiO2 had the most effective and stable performance as the nucleators for hydrate salts. The analysis of FT-IR showed that there were strong characteristic hydroxyl bonds on the surface of Aerosol SiO2. And the designed hydroxyl controllable silica gel system could prove the effect of hydroxyl bonds on suppressing supercooling of hydrate salts. It was concluded that supercooling of hydrate salts could be easily suppressed by the nano-additives with high specific surface area and strong polar hydroxyls in the surface. The ion-exchange attraction between hydroxyls and hydrate salts might mainly result in the supersaturation of hydrate salts in the interface of nano-particles. And then the supercooling of hydrate salts could be suppressed. The theoretical analysing model based on interionic attraction is a novel approach for investigating the nucleation of hydrate salts. And this result might provide a potential low-cost approach for the applications of nano-additives in building energy storage and coolant.

  3. Fe-N-C electrocatalysts for oxygen reduction reaction synthesized by using aniline salt and Fe3+/H2O2 catalytic system

    KAUST Repository

    Bukola, Saheed

    2014-11-01

    Non-precious metal (NPM) catalysts are synthesized by polymerizing aniline salt using an aqueous Fe3+/H2O2 coupled catalytic system on a carbon matrix with a porous creating agent. The sulfur containing compunds such as ammonium peroxydisulfate, are eliminated in this method resulting in a much simpler process. The catalysts\\' porous structures are enhanced with ammonium carbonate as a sacrificial material that yields voids when decomposed during the heat treatment at 900 °C in N2 atmosphere. Two catalysts Fe-N-C/Vu and Fe-N-C/KB (Vu = Vulcan and KB = Ketjen black) were synthesized and characterized. Their oxygen reduction reaction (ORR) activities were investigated using a rotating ring-disk electrode (RRDE) in both 0.1 M KOH and 0.1 M HClO4. The catalysts show improved ORR activities close to that of Pt-based catalysts, low H2O2 formation and also demonstrated a remarkable tolerance towards methanol oxidation.

  4. Thermodynamic investigation of the ternary mixed aqueous electrolyte (MgCl2 + MgSO4) system by potentiometric method at T = 298.15 K

    International Nuclear Information System (INIS)

    Highlights: → In this study we investigated the thermodynamic properties of MgCl2 + MgSO4 + H2O. → The method used in this work was potentiometric method. → Mg-ISE and the Ag/AgCl electrodes used in this work had a good Nernst response. → The experimental results obeyed the Harned rule. → The Pitzer model could be used to describe this ternary system satisfactorily. - Abstract: This work reports the results of thermodynamic investigation of the ternary mixed-electrolyte system (MgCl2 + MgSO4 + H2O). The investigation was performed based on Pitzer ion interaction model by using the potentiometric technique at T = 298.15 K. The mean activity coefficients of MgCl2 in the mixed aqueous electrolyte system were determined on the galvanic cell without liquid junction of the type: Mg-ISE|MgCl2 (mA), MgSO4 (mB), H2O|Ag/AgCl over total ionic strengths from (0.001 to 8.000) mol . kg-1 for different series of salt ratio r (r=mMgCl2/mMgSO4=2.5,5.0,7.5,10.0,15.0 and pure MgCl2). The PVC based magnesium ion-selective electrode (Mg-ISE) and the Ag/AgCl electrode used in this work were made in our laboratory and had a reasonably good Nernst response. The experimental results obeyed the Harned rule, and the Pitzer model could be used to describe this ternary system satisfactorily. Pitzer ion-interaction parameters for mixed salts were determined for this system. Then, these parameters (θClSO4=0.0252±0.0042, ψMgClSO4=-0.0049±0.0003) were used to calculate the values of the mean activity coefficients of MgSO4, the osmotic coefficients of water (φ) and the excess Gibbs free energies of solution (GE) for the whole series of the studied electrolyte systems.

  5. Phase diagram of uranyl acetate-water-tri-n-butyl phosphate system in the region of high salt concentrations

    International Nuclear Information System (INIS)

    The results of investigations into mutual solubility in the system of uranyl acetate-water-tributyl phosphate (the range of high salt concentrations) at 25 deg C are presented. The phase diagram of the system in the solubility range is shown to differ sharply from the most of diagrams of the known systems of salt-water-tributyl phosphate. An attempt is made to associate the unusual character of the solubility isotherm with change of the role of water in extraction and dissolution processes at transition from halogenoacetates to uranyl acetate. Based on IR spectroscopic data the conclusion is made on uranyl acetate solvation in the organic phase only with one molecule of tributyl phosphate, but not two molecules, as it was considered earlier

  6. Cytogenotoxicity of Cymbopogon citratus (DC) Stapf (lemon grass) aqueous extracts in vegetal test systems

    OpenAIRE

    Saulo M. Sousa; Pâmela S. Silva; Lyderson F. Viccini

    2010-01-01

    The lemon grass, Cymbopogon citratus (DC) Stapf, is an important species of Poaceae family commonly used in the folk medicine in many countries. The aim of this study was to investigate the cytotoxic and genotoxic effects of aqueous extracts from C. citratus leaves on Lactuca sativa (lettuce) root tip meristem cells by cytogenetic studies that have never been done before for lemon grass extracts. For this, lettuce seeds were treated for 72h with different concentrations of lemon grass aqueous...

  7. Extraction, Preconcentration and Isolation of Flavonoids from Apocynum venetum L. Leaves Using Ionic Liquid-Based Ultrasonic-Assisted Extraction Coupled with an Aqueous Biphasic System

    Directory of Open Access Journals (Sweden)

    Zhijian Tan

    2016-03-01

    Full Text Available Background: Ionic liquids (ILs are considered as green solvents, and widely applied for the extraction of various compounds. Methods: The present research focuses on the extraction of flavonoids from Apocynum venetum L. leaves by ultrasound-assisted extraction (UAE. Several major influencing factors were optimized. Then, an aqueous biphasic system (ABS was applied for further isolation of flavonoids. Results: The flavonoids were mainly distributed in the top phase, while impurities were extracted to the bottom phase. The parameters influencing the extraction, namely type and concentration of salt, temperature, and pH, were studied in detail. Under optimized conditions (72.43% IL extract, 28.57% (NH42SO4, 25 °C temperature, pH 4.5, the preconcentration factor and extraction efficiency were found to be 3.78% and 93.35%, respectively. Conclusions: This simple and efficient methodology is expected to see great use in the extraction and isolation of pharmaceutically active components from medicinal plant resources.

  8. Aqueous Two-phase Systems with Ultrasonic Extraction Used for Extracting Phenolic Compounds from Inonotus obliquus

    Institute of Scientific and Technical Information of China (English)

    ZHAO; Yan-xia; LIU; Yu-bing; LIU; Feng; ZHENG; Wei-fa

    2013-01-01

    Objective To optimize the extracting technology of assessing the maximum yield of phenolic compounds (PC) from Inonotus obliquus by single factor experiments and orthogonal array design methods through aqueous two-phase systems combined with ultrasonic extraction. Methods The range of the independent variables, namely levels of acetone and ammonium sulfate, and ultrasonic time were identified by a first set of single factor experiments. The actual values of the independent variables coded at four levels and three factors were selected based on the results of the single factor experiments. Subsequently, the levels of acetone and ammonium sulfate, and ultrasonic time were optimized using the orthogonal array method. Results The optimum conditions for the extraction of PC were found to use 7.0 mL acetone, 5.5 mg ammonium sulfate, with ultrasonic time for 5 min. Under these optimized conditions, the experimental maximum yield of PC was 37.8 mg/g, much higher than that of the traditional ultrasonic extraction (UE, 29.0 mg/g). And the PC obtained by this method had stronger anti-oxidative activities than those by traditional UE method. Conclusion These results indicate the suitability of the models developed and the success in optimizing the extraction conditions. This is an economical and efficient method for extracting polyphenols from I. obliquus.

  9. Aqueous Two-phase Systems with Ultrasonic Extraction Used for Extracting Phenolic Compounds from Inonotus obliquus

    Institute of Scientific and Technical Information of China (English)

    ZHAO Yan-xia; LIU Yu-bing; LIU Feng; ZHENG Wei-fa

    2013-01-01

    Objective To optimize the extracting technology of assessing the maximum yield of phenolic compounds (PC)from Inonotus obliquus by single factor experiments and orthogonal array design methods through aqueous two-phase systems combined with ultrasonic extraction.Methods The range of the independent variables,namely levels of acetone and ammonium sulfate,and ultrasonic time were identified by a first set of single factor experiments.The actual values of the independent variables coded at four levels and three factors were selected based on the results of the single factor experiments.Subsequently,the levels of acetone and ammonium sulfate,and ultrasonic time were optimized using the orthogonal array method.Results The optimum conditions for the extraction of PC were found to use 7.0 mL acetone,5.5 mg ammonium sulfate,with ultrasonic time for 5 min.Under these optimized conditions,the experimental maximum yield of PC was 37.8 mg/g,much higher than that of the traditional ultrasonic extraction (UE,29.0 mg/g).And the PC obtained by this method had stronger anti-oxidative activities than those by traditional UE method.Conclusion These results indicate the suitability of the models developed and the success in optimizing the extraction conditions.This is an economical and efficient method for extracting polyphenols from Ⅰ.obliquus.

  10. Wash Solution Bath Life Extension for the Space Shuttle Rocket Motor Aqueous Cleaning System

    Science.gov (United States)

    Saunders, Chad; Evans, Kurt; Sagers, Neil

    1999-01-01

    A spray-in-air aqueous cleaning system, which replaced 1,1,1 trichloroethane (TCA) vapor degreasing, is used for critical cleaning of Space Shuttle Redesigned Solid Rocket Motor (RSRM) metal parts. Small-scale testing demonstrated that the alkaline-based wash solution possesses adequate soil loading and cleaning properties. However, full-scale testing exhibited unexpected depletion of some primary components of the wash solution. Specifically, there was a significant decrease in the concentration of sodium metasilicate which forced change-out of the wash solution after eight days. Extension of wash solution bath life was necessary to ease the burden of frequent change-out on manufacturing. A laboratory study supports a depletion mechanism that is initiated by the hydrolysis of sodium tripolyphosphate (STPP) lowering the pH of the solution. The decrease in pH causes polymerization and subsequent precipitation of sodium metasilicate (SM). Further investigation showed that maintaining the pH was the key to preventing the precipitation of the sodium metasilicate. Implementation to the full scale operation demonstrated that periodic additions of potassium hydroxide (KOH) extended the useful bath life to more than four months.

  11. Multi-equilibrium system based on sertraline and β-cyclodextrin supramolecular complex in aqueous solution.

    Science.gov (United States)

    Passos, Joel J; De Sousa, Frederico B; Lula, Ivana S; Barreto, Elison A; Lopes, Juliana Fedoce; De Almeida, Wagner B; Sinisterra, Rubén D

    2011-12-12

    Sertraline (SRT) is a widely used antidepressant whose poor solubility in water limits its oral applicability. Thus, the aim of this work was the evaluation of a multi-equilibrium system based on β-cyclodextrin (βCD) and SRT. The inclusion compounds (ICs) were investigated by infrared spectroscopy, isothermal titration calorimetry (ITC) and (1)H and 2D ROESY nuclear magnetic resonance experiments. SRT solubility was predicted in vitro in water and biomimetic fluids. The SRT in presence of βCD at 1:1 and 1:2 molar ratios was more soluble than free SRT in all biomimetics media investigated. The FTIR-HATR showed that βCD νC-O-C stretching band was reduced in presence of SRT, suggesting the interactions between them. Additionally, titration process and Job's plot provided information on the ICs stoichiometry and evidenced the multi-equilibrium coexistence in aqueous solution. According to the ITC, SRT:βCD interaction process was spontaneous and exothermic with a high affinity binding constant (K=14,726 M(-1)). Additionally, the stoichiometry coefficient (n) was 1.63, which was comparable to that found by FITR-HATR. The (1)H and 2D ROESY verified multiple SRT sites included into the host cavity. Theoretical calculations depicted the relative energy of different proposed ICs structures, in which the 1:2 IC was the most stable. PMID:21963467

  12. Partitioning in aqueous two-phase systems: Analysis of strengths, weaknesses, opportunities and threats.

    Science.gov (United States)

    Soares, Ruben R G; Azevedo, Ana M; Van Alstine, James M; Aires-Barros, M Raquel

    2015-08-01

    For half a century aqueous two-phase systems (ATPSs) have been applied for the extraction and purification of biomolecules. In spite of their simplicity, selectivity, and relatively low cost they have not been significantly employed for industrial scale bioprocessing. Recently their ability to be readily scaled and interface easily in single-use, flexible biomanufacturing has led to industrial re-evaluation of ATPSs. The purpose of this review is to perform a SWOT analysis that includes a discussion of: (i) strengths of ATPS partitioning as an effective and simple platform for biomolecule purification; (ii) weaknesses of ATPS partitioning in regard to intrinsic problems and possible solutions; (iii) opportunities related to biotechnological challenges that ATPS partitioning may solve; and (iv) threats related to alternative techniques that may compete with ATPS in performance, economic benefits, scale up and reliability. This approach provides insight into the current status of ATPS as a bioprocessing technique and it can be concluded that most of the perceived weakness towards industrial implementation have now been largely overcome, thus paving the way for opportunities in fermentation feed clarification, integration in multi-stage operations and in single-step purification processes. PMID:26213222

  13. Optimization of Biosorptive Removal of Dye from Aqueous System by Cone Shell of Calabrian Pine

    Directory of Open Access Journals (Sweden)

    Fatih Deniz

    2014-01-01

    Full Text Available The biosorption performance of raw cone shell of Calabrian pine for C.I. Basic Red 46 as a model azo dye from aqueous system was optimized using Taguchi experimental design methodology. L9 (33 orthogonal array was used to optimize the dye biosorption by the pine cone shell. The selected factors and their levels were biosorbent particle size, dye concentration, and contact time. The predicted dye biosorption capacity for the pine cone shell from Taguchi design was obtained as 71.770 mg g−1 under optimized biosorption conditions. This experimental design provided reasonable predictive performance of dye biosorption by the biosorbent (R2: 0.9961. Langmuir model fitted better to the biosorption equilibrium data than Freundlich model. This displayed the monolayer coverage of dye molecules on the biosorbent surface. Dubinin-Radushkevich model and the standard Gibbs free energy change proposed physical biosorption for predominant mechanism. The logistic function presented the best fit to the data of biosorption kinetics. The kinetic parameters reflecting biosorption performance were also evaluated. The optimization study revealed that the pine cone shell can be an effective and economically feasible biosorbent for the removal of dye.

  14. Sustainable AC/AC hybrid electrochemical capacitors in aqueous electrolyte approaching the performance of organic systems

    Science.gov (United States)

    Abbas, Qamar; Babuchowska, Paulina; Frąckowiak, Elżbieta; Béguin, François

    2016-09-01

    A high energy hybrid AC/AC electrochemical capacitor has been realized in aqueous Li2SO4+KI electrolyte mixture. Owing to the redox processes associated with the 2I-/I2 system, the positive electrode operates in narrow potential range and displays high capacity. During prolonged potentiostatic floating at 1.6 V, the hybrid cell demonstrates remarkably stable capacitance and resistance. Analyses by temperature programmed desorption after floating at 1.6 V proved that oxidation of the positive AC electrode is prevented by the use of Li2SO4+KI, which enables the maximum potential of this electrode to be shifted below the water oxidation potential. When charged at 0.2 A g-1 up to U = 1.6 V, the hybrid cell displays a high capacitance of 75 F g-1 (300 F g-1 per mass of one electrode) compared to 47 F g-1 (188 F g-1 per mass of one electrode) for a symmetric cell in Li2SO4. At 0.2 A g-1 up to 1.6 V, the hybrid capacitor in Li2SO4+KI displays an energy density of 26 Wh kg-1 which approaches the energy density of 30.9 Wh kg-1 measured when the same carbon is implemented in a capacitor using TEABF4/ACN electrolyte and charged up to 2.5 V.

  15. Environmental fate of spinosad. 1. Dissipation and degradation in aqueous systems.

    Science.gov (United States)

    Cleveland, Cheryl B; Bormett, Gary A; Saunders, Donald G; Powers, Fred L; McGibbon, Alec S; Reeves, Graham L; Rutherford, Laura; Balcer, Jesse L

    2002-05-22

    Spinosad is a bacterially derived insect control agent consisting of two active compounds, spinosyns A and D. The objective of this paper is to describe the environmental fate of spinosad in aquatic systems. To this end, several studies performed to meet regulatory requirements are used to study the fate and degradation in individual environmental media. Specifically, investigations of abiotic (hydrolysis and photolysis) and biotic (aerobic and anaerobic aquatic) processes are described. Understanding developed from the laboratory-based studies has been tested and augmented by an outdoor microcosm study. Understanding of aquatic fate is a building block for a complete environmental safety assessment of spinosad products (Cleveland, C. B.; Mayes, M. A.; Cryer, S. A. Pest Manag. Sci. 2001, 58, 70-84). From individual investigations, the following understanding of dissipation emerges: (1) Aqueous photolysis of spinosad is rapid (observed half-lives of spinosyn aglycon degradates. (3) Hydrolytic degradation involves loss of the forosamine sugar and water and reduction on the macrolide ring to a double bond at the 16,17-position. PMID:12009994

  16. Self-assembly of aqueous bilirubin ditaurate, a natural conjugated bile pigment, to contraposing enantiomeric dimers and M(-) and P(+) tetramers and their selective hydrophilic disaggregation by monomers and micelles of bile salts.

    Science.gov (United States)

    Neubrand, Michael W; Carey, Martin C; Laue, Thomas M

    2015-02-24

    The solution behavior of bilirubin ditaurate (BDT), the first naturally occurring conjugated bile pigment to be physically and chemically characterized, was assessed in aqueous solution and in monomeric and micellar solutions of common taurine-conjugated bile salts (BS). Analytical ultracentrifugation revealed that BDT self-associates in monomer-dimer equilibria between 1 and 500 μM, forming limiting tetramers at low millimolar concentrations. Self-association was enthalpically driven with ΔG values of ≈5 kcal/mol, suggesting strong hydrophobic interactions. Added NaCl and decreases in temperature shifted the oligomerization to lower BDT concentrations. On the basis of circular dichroism spectra and the limiting size of the self-aggregates, we infer that the tetramers are composed of 2P(+) and 2M(-) enantiomeric BDT pairs in "ridge-tile" conformations interacting in a "double-bookend" structure. With added monomeric BS, blue shifts in the UV-vis spectra and tight isosbestic points revealed that BDT/BS heterodimers form, followed by BDT "decorating" BS micelles mostly via hydrophilic interactions. Conformational enantiomerism, fluorescence intensities, and anisotropy, as well as resistance of the hybrid particles to disaggregation in 6 M urea, suggested that two or three hydrogen-bonding sites bound BDT monomers to the hydroxyl groups of BS, possibly via pyrrole-π-orbital-OH interactions. BDT stabilized these interactions by enveloping the BS in its "ridge-tile" pincers with variable strain that maximized van der Waals interactions. Possibly because the BDT molecule becomes highly strained with BS subtending a 7β-hydroxyl group, BDT became totally resistant to oxidation in air. This work predicts that, because of BS dissolution of the BDT self-aggregates, BS/bilirubin hybrid particles, which are stabilized hydrophilically, are likely to be the dominant mode of transport for all conjugated bilirubins in bile. PMID:25671490

  17. Extraction of lanthanides ions (III) from aqueous solution by sodium salt of the N(4-amino-benzoate)-propyl-silica gel

    International Nuclear Information System (INIS)

    The silica gel 60 of specific superficial area 486 m2.g-1 was modified chemically with the ligand 4-amino benzoate of sodium in water-ethanol environment (l:L). The adsorptions of metallic ions were from water solutions at approximately 2 x 10-3 M of chloride of Pr(III), Nd(III), Eu(III) and Ho(III). In these experiments we could see that the system gets the equilibrium of adsorption rapidly and that the pH of the environment has a great influence on the process of adsorption, being that the number of metal mols adsorpted in the matrix varied between 10,00 and 17,00 x 10-5 mols. g-1 with a pH of approximately 5 for all the lanthanides, where the adsorption curves reach equilibrium. (author)

  18. [Bmim]Cl双水相体系对猪皮皮粉溶解性能的研究%The Dissolvability of Pigskin Hide Powder in the [Bmim] Cl Aqueous Two-phase System

    Institute of Scientific and Technical Information of China (English)

    邹永鹏; 刘森; 冯健; 华坚; 周华龙

    2012-01-01

    实验以溴代正丁烷和N-甲基咪唑为原料,丙酮为溶剂合成目标离子液体氯化1-丁基-3-甲基咪唑([Bmim]Cl).将合成的[Bmim]Cl、盐和去离子水混合形成离子液体双水相体系,并溶解猪皮皮粉.讨论不同种类的盐和不同质量分数的猪皮皮粉溶于猪皮皮粉溶于离子液体双水相体系的溶解情况.通过研究发现双水相体系中,盐为K2HPO4且浓度为65.5mg/mL时溶解猪皮胶原情况最好,平且当猪皮皮粉的质量分数为10%时,溶液已经达到饱和.用傅里叶红外光谱仪对回收的离子液体以及猪皮胶原再生膜进行红外分析,观察得到回收的离子液体的较好,猪皮皮粉溶解前后胶原二级结构未发生变化.%[Bmim]Cl was synthesized by n-butyl bromide and N-methylimidazole, with acetone as the solvent. [Bmim] Cl, salt and deionized water were mixed to form ionic liquids aqueous two-phase system which dissolved pigskin hide powder. The different kinds of salt and the different mass fraction pigskin hide powder were studied and characterized respectively, influencing the dissolvability of pigskin hide powder in ionic liquids aqueous two-phase system. It showed that salt in the aqueous two-phase system for K2HPO4 and for 62.5 mg/mL dissolved pigskin collagen when it was best. What' s more, when the dosage of pigskin hide powder was 11%, the solution had already saturated. FT1R spectra was used to observe the recycled ionic liquids and the regeneration of pigskin collagen. The recycled ionic liquid was well, and the , regeneration of pigskin collagen of the secondary structure of collagen didn' t changed.

  19. Study of an aqueous lithium chloride desiccant system Part II: Desiccant regeneration

    Energy Technology Data Exchange (ETDEWEB)

    Fumo, Nelson [Universidad Nacional Experimental del Tachira, San Cristobal (Venezuela); Goswami, Yogi [University of Florida, Gainesville (United States)

    2000-07-01

    Desiccant systems have been proposed as alternative to handle the latent load in vapor compression air conditioning for energy saving. The air dehumidification occurs because of the difference in vapor pressure which let the moisture diffuse from the air to the liquid desiccant. The diffused moisture cause a dilution of the desiccant which must be regenerated to return it to the original conditions. This paper presents the results from a study of the performance of a packed tower regenerator for an aqueous lithium chloride desiccant dehumidification system. The rate of water evaporation, as well as the effectiveness of the regeneration process were assessed under the effects of variables such as air and desiccant flow rates, air temperature and humidity, and desiccant temperature and concentration. A variation of the oeberg and Goswami mathematical model was used to predict the experimental findings given satisfactory results. [Spanish] Se han propuesto sistemas desecantes para hacerse cargo de la carga latente en acondicionamiento de aire por compresion de vapor para el ahorro de energia. La deshumidificacion del aire ocurre en razon de la diferencia de presion de vapor que deja la humedad difusa del aire en el desecante liquido. La humedad difusa del aire origina una dilucion del desecante el cual debe de ser regenerado para regresarlo a sus condiciones originales. Este documento presenta los resultados de un estudio sobre el comportamiento de un regenerador de torre empacada para un sistema de deshumidificacion de solucion desecante de cloruro de litio. El regimen de evaporacion de agua, asi como tambien la efectividad del proceso de regeneracion que se evaluo bajo los efectos de variables tales como los regimenes de flujo de aire y de desecante, temperatura del aire y humedad, y temperatura y concentracion del desecante. Una variacion del modelo matematico de Oberg y Goswami se uso para predecir los resultados experimentales que dieron resultados satisfactorios.

  20. Study of an aqueous lithium chloride desiccant system Part I: Air dehumidification

    Energy Technology Data Exchange (ETDEWEB)

    Fumo, Nelson [Universidad Nacional Experimental del Tachira, San Cristobal (Venezuela); Goswami, Yogi [University of Florida, Gainesville (United States)

    2000-07-01

    Desiccant systems have been proposed as energy saving alternative to vapor compression air conditioning for handling the latent load. Use of liquid desiccants offers several design and performance advantages over solid desiccants, especially when solar energy is used for regeneration. For liquid-gas contact, packed towers with low pressure drop have offered good heat and mass transfer characteristics for compact designs. This paper presents the results from a study of the performance of a packed tower absorber for an aqueous lithium chloride desiccant dehumidification system. The rate of dehumidification, as well as the effectiveness of the dehumidification process were assessed under the effects of variables such as air and desiccant flow rates, air temperature and humidity, and desiccant temperature and concentration. A variation of the oeberg and Goswami mathematical model was used to predict the experimental findings given satisfactory results. [Spanish] Se han propuesto sistemas de desecacion como una alternativa de ahorro de energia para el acondicionamiento de aire mediante la compresion de vapor para manejar la carga latente. El uso de desecantes liquidos ofrece varias ventajas de diseno y de rendimiento sobre los desecantes solidos, especialmente cuando la energia solar se usa para la regeneracion. Para el contacto liquido-gas han dado buenas caracteristicas de transferencia de masa para disenos compactos las torres empacadas con baja caida de presion. Este documento presenta los resultados de un estudio del comportamiento de un absorbedor de torre empacada para una solucion acuosa de desecante de cloruro de litio como sistema de deshumidificacion. El regimen de deshumidificacion asi como tambien la eficiencia del proceso de deshumidificacion se evaluo bajo los efectos de variables tales como regimenes de flujo de aire y de desecante, temperatura del aire y humedad, y concentracion y temperatura del desecante. Se uso una variante de modelo matematico de

  1. Phase equilibria in the system H{sub 2}O-NaCl-KCl-MgCl{sub 2} relevant to salt cake processing

    Energy Technology Data Exchange (ETDEWEB)

    Bodnar, R.J.; Vityk, M.O. [Virginia Polytechnic Inst., Blacksburg, VA (United States); Hryn, J.N. [Argonne National Lab., IL (United States); Mavrogenes, J. [Australian National Univ., Canberra, ACT (Australia)

    1997-02-01

    One waste product in recycling of Al is salt cake, a mixture of Al, salts, and residue oxides. Several methods have been proposed to recycle salt cake, one involving high-temperature leaching of salts from the salt cake. The salt composition can be approximated as a mixture predominantly of NaCl and KCl salts, with lesser amounts of Mg chloride. In order to better assess the feasibility of recycling salt cake, an experimental study was conducted of phase equilibria in the system H{sub 2}O-NaCl-KCl-MgCl{sub 2} at pressure (P), temperature (T), and composition conditions appropriate for high- temperature salt cake recycling. These experiments were designed to evaluate the effect of small amounts (2-10 wt%) of MgCl{sub 2} on solubilities of halite (NaCl) and sylvite (KCl) in saturated solutions (30-50 wt% NaCl+KCl; NaCl:KCl = 1:1 and 3:1) at elevated P and T.

  2. Conceptual design of retrieval systems for emplaced transuranic waste containers in a salt bed depository. Final report

    International Nuclear Information System (INIS)

    The US Department of Energy and the Nuclear Regulatory Commission have jurisdiction over the nuclear waste management program. Design studies were previously made of proposed repository site configurations for the receiving, processing, and storage of nuclear wastes. However, these studies did not provide operational designs that were suitable for highly reliable TRU retrieval in the deep geologic salt environment for the required 60-year period. The purpose of this report is to develop a conceptual design of a baseline retrieval system for emplaced transuranic waste containers in a salt bed depository. The conceptual design is to serve as a working model for the analysis of the performance available from the current state-of-the-art equipment and systems. Suggested regulations would be based upon the results of the performance analyses

  3. Theoretical Studies of Aqueous Systems above 25 deg C. 2. The Iron - Water System

    International Nuclear Information System (INIS)

    A theoretical study of the iron-water system at elevated temperatures is reported. Values for the equilibrium constants for the principle reactions in the system up to 374 deg C, obtained by a method described previously, are given and equilibrium diagrams are presented that illustrate the results for 50, 150, 250 and 350 deg C. The results indicate that, among other things, the most important metal-bearing ions in the iron-water system at elevated temperatures are Fe(OH)2+, Fe(OH)+ and HFeO2- The conditions for the stability of solid iron oxides are also examined. Finally, some limitations of the thermodynamic approach to corrosion problems are discussed briefly

  4. System for absolute measurement of electrolytic conductivity in aqueous solutions based on van der Pauw's theory

    International Nuclear Information System (INIS)

    Based on an innovative application of van der Pauw's theory, a system was developed for the absolute measurement of electrolytic conductivity in aqueous solutions. An electrolytic conductivity meter was designed that uses a four-electrode system with an axial–radial two-dimensional adjustment structure coupled to an ac voltage excitation source and signal collecting circuit. The measurement accuracy, resolution and repeatability of the measurement system were examined through a series of experiments. Moreover, the measurement system and a high-precision electrolytic conductivity meter were compared using some actual water samples. (paper)

  5. Development of system analysis code for pyrochemical process using molten salt electrorefining

    International Nuclear Information System (INIS)

    This report describes accomplishment of development of a cathode processor calculation code to simulate the mass and heat transfer phenomena with the distillation process and development of an analytical model for cooling behavior of the pyrochemical process cell on personal computers. The pyrochemical process using molten salt electrorefining would introduce new technologies for new fuels of particle oxide, particle nitride and metallic fuels. The cathode processor calculation code with distillation process was developed. A code validation calculation has been conducted on the basic of the benchmark problem for natural convection in a square cavity. Results by using the present code agreed well for the velocity-temperature fields, the maximum velocity and its location with the benchmark solution published in a paper. The functions have been added to advance the reality in simulation and to increase the efficiency in utilization. The test run has been conducted using the code with the above modification for an axisymmetric enclosed vessel simulating a cathode processor, and the capability of the distillation process simulation with the code has been confirmed. An analytical model for cooling behavior of the pyrochemical process cell was developed. The analytical model was selected by comparing benchmark analysis with detailed analysis on engineering workstation. Flow and temperature distributions were confirmed by the result of steady state analysis. In the result of transient cooling analysis, an initial transient peak of temperature occurred at balanced heat condition in the steady-state analysis. Final gas temperature distribution was dependent on gas circulation flow in transient condition. Then there were different final gas temperature distributions on the basis of the result of steady-state analysis. This phenomenon has a potential for it's own metastable condition. Therefore it was necessary to design gas cooling flow pattern without cooling gas circulation

  6. Water sorption on silica- and zeolite-supported hygroscopic salts for cooling system applications

    International Nuclear Information System (INIS)

    Highlights: ► The silica- and zeolite-supported hygroscopic salts (SHS) were prepared. ► The water uptake was evaluated as function of the pore size and salt content. ► A novel method based on mass spectrometry (MS) was proposed and successfully used. ► The MS was applied to obtain the water sorption isobars on SHS. ► The thermodynamic cooling cycle for SHS–water pair showed a coefficient of performance of 0.83. - Abstract: Silica gel and zeolite 13X were used as supports for the hygroscopic salts LiBr, MgCl2 and CaCl2. The silica- and zeolite-supported hygroscopic salts were characterized by N2 adsorption at −196 °C and X-ray diffraction. The silica support was mesoporous whereas the zeolite support was microporous. The dispersion of CaCl2 was much lower on the zeolite than on the silica support, and the microporosity of the zeolite was blocked by the salt. CaCl2 supported on silica was a superior water sorbent versus zeolite, and CaCl2 supported on zeolite was an inferior sorbent versus zeolite. Complete water desorption from silica-supported hygroscopic salts can be effectively reached at a relatively low temperature (100–110 °C), making them candidates for efficient cooling or air conditioning applications. The isosteric heat of water desorption was obtained from the isobars and was dependent on the amount of water adsorbed. Finally, the thermodynamic cooling cycle for the SCa33 (silica gel containing 33 wt.% CaCl2) – water vapour pair showed a coefficient of performance of 0.83.

  7. Process and system for reducing the inactive salt concentration in waste solutions of nuclear power plants

    International Nuclear Information System (INIS)

    The method is based on a suitable combination of most modern separation measures as there are precipitation, filtration, ultra-filtration, reverse osmosis, ion exchange, evaporation and crystallization; in this method almost the total quantity of the components with radioactivity, except tritium, can be effectively separated from inactive salts. One part of the inactive salt (alkali nitrate) can be treated as industrial waste and the other part (boric acid) can be recycled. The method of the invention as well as the equipment used for its execution can considerably reduce the high costs of waste solution treatment in nuclear power stations. (orig./RB)

  8. Partition of lead in milk-pectin aqueous biphasic system with complexation agents

    International Nuclear Information System (INIS)

    In present work, decontamination of raw cow milk from lead was investigated using the 'membraneless dialysis'. The 4% w/w solutions of apple pectin, degree of esterification 70%, containing various complexing agents were used for experiments at the initial volume ration pectin : milk = 3:7 which changed to 8:2 at equilibration. Radioactive indicator 212Pb was prepared from 228Th emanator. After dissolution in Jennes-Koops buffer with 10-5 M Pb2+ carrier, milk was spiked with the indicator for 100 minutes. Distribution equilibrium of water and lead was achieved after next 100 minutes but yield of lead extraction into pectin phase was less then 2.3% in the case of raw milk, and less then 3.0% in the case of pasteurized milk. Due to denaturation of raw milk, there are strongly limited possibilities to influence the radionuclide partition in the systems. Various non-toxic complexation agents (glycine, alanine, histidine, cysteine, Edtacal) were applied to improve extraction of lead to pectin phase. Glycine and histidine have not influence on lead extraction yields but there was observed an increased yield, 3,8% for alanine and even 25% for 0.002 M cysteine. As the most interesting appeared application of Edtacal, calcium salt of ethylenediaminetetraacetic acid, EDTA by which the recovery of lead with with pectin phase reached about 80% at concentration of EDTA in initial pectin phase 0.001 M. The retention of Pb2+ cation in milk phase is extraordinary high as compared with strontium and corresponds to behavior of trivalent ions what is attributed to specific interactions with thiol groups of milk components

  9. An easily operated apparatus to register the amount of the aqueous solution absorbed by a plant root system

    Directory of Open Access Journals (Sweden)

    Jerzy Czerski

    2015-05-01

    Full Text Available An easily operated apparatus was constructed (figs. 1,2 allowing to register the amount of the aqueous solution absorbed by a planet root system. The device allows for simultaneous registering of the solution absorption by two plants. The recording of a definite volume of the absorbed solution can be controlled within wide limits. Experiments (figs. 3,4 confirmed the efficiency of the apparatus.

  10. Aqueous two-phase micellar systems in an oscillatory flow micro-reactor: Study of perspectives and experimental performance

    OpenAIRE

    A. M. LOPES; Silva, Daniel Pereira da; A.A. Vicente; Pessoa Júnior, Adalberto; Teixeira, J. A.

    2011-01-01

    Aqueous two-phase micellar systems (ATPMS) are micellar surfactant solutions with physical properties that make them very efficient for the extraction/concentration of biological products. In this work the main proposal that has been discussed is the possible applicability and importance of a novel oscillatory flow micro-reactor (micro-OFR) envisaged for parallel screening and/or development of industrial bioprocesses in ATPMS. Based on the technology of oscillatory flow mixing (OFM), this ba...

  11. Synthesis and NMR characterization of SAPO-35 from non-aqueous systems using hexamethyleneimine template

    International Nuclear Information System (INIS)

    SAPO-35 was synthesized using hexamethyleneimine template in non-aqueous systems. X-ray diffraction and scanning electron micrograph analysis shows the synthesized sample is pure and well crystalline. Presence of four stages (1.6%, 0.8%, 7.8% and 8.4%) of weight loss is observed by TG/DTA analysis. FT-IR analysis in the framework region shows the presence of tetrahedral T-O-T vibrations is similar to the other known aluminophosphate molecular sieves. FT-IR spectrum in the -OH region shows stretching vibrations at 3631, 3604 and 3580 cm-1 can be assigned to OH groups in bigger cages near S6R, in bigger cages near D6R and those actually confined inside the D6R, respectively. The spectra for the as-synthesized sample show a single symmetrical 27Al MAS NMR line at δ = 36.26 indicating the presence of a single tetrahedral aluminium species. Where as 29Si and 31P MAS NMR shows the presence of two peaks in both at (-89.9 and -95.15 ppm) and (-34.01 and -40.45 ppm) due to the Si substitution of P present in two different locations in double 6 ring (D6R) and in single 6 ring (S6R). 27Al 3Q-MAS NMR shows two peaks for environmentally different tetrahedral aluminium atoms. This is the first time we are showing such a fact which is not observable using ordinary MAS NMR

  12. Stable thermosensitive in situ gel-forming systems based on the lyophilizate of chitosan/α,β-glycerophosphate salts.

    Science.gov (United States)

    Wu, Guanghao; Yuan, Yuan; He, Jintian; Li, Ying; Dai, Xiaojing; Zhao, Baohua

    2016-09-10

    In the present study, lyophilization was attempted to improve the long-term storage of CS/GP thermogelling systems for biopharmaceutical applications. After lyophilization, CS/α,β-GP lyophilizate could not be dissolved in water, but some metal salts, such as NaCl, CaCl2, and MgCl2 surprisingly facilitated its dissolution. X-ray powder diffraction analysis suggested that calcium ions might preferentially form salts with α,β-GP, inhibit the transfer of protons from CS to α,β-GP, and then inhibit the aggregation of CS molecules during lyophilization. Comparison of the freshly prepared CS/α,β-GP/salt solutions and the reconstituted solutions from lyophilizates showed that lyophilization clearly influenced the properties of reconstituted CS/α,β-GP/salt solutions such as gelation time, viscosity, and pH. Furthermore, the reconstituted CS/α,β-GP/CaCl2 solutions maintained thermogelling properties and formed hydrogels at 37°C within approximately 5min, but did not form hydrogels at 20°C and 4°C over 2 weeks. The model protein bovine serum albumin (BSA) was further incorporated into the CS/α,β-GP/CaCl2 system. In vitro release experiments showed the sustained release of BSA from CS/α,β-GP/CaCl2 hydrogels in a pH-sensitive manner, demonstrating that CS/α,β-GP/CaCl2 may be useful as an in situ gel-forming system. PMID:27457422

  13. Chromatography of 49 metal ions on stannic antimonate papers in dimethylsulfoxide: nitric acid systems and aqueous nitric acid systems

    International Nuclear Information System (INIS)

    Chromatographic separations of 49 metal ions on stannic antimonate papers have been performed using mixed solvent systems containing DMSO. Aqueous HNO3 systems have also been used. The utility of the papers has been demonstrated by achieving various difficult separations. Some of the important separations (R/sub f/ values given in parentheses) are: Cs+(0.20)-K+(0.30) and Sm3+(0.00)-Pr3+(0.72) in pure DMSO; Nb5+(0.14)-VO2+(0.95) in DMSO-6M HNO3 (1:1); Ti4+(0.00)-VO2(0.97) in DMSO-0.5M HNO3 (1:1); and Ba2+(0.06)-K+(0.52)-Sr2+(0.95), Ba2+(0.04)-Cs+(0.41)-Mg2+(0.93), and Ca2+(0.10)-Sr2+(0.94) in DMSO-0.1M HNO3 (1:1). The time of development in each case is two hours. A discussion is presented on the dependence of Ri, log R/sub f/, and R/sub M/ on pH of the solvent to understand the mechanism of the movement of metal ions on papers impregnated with inorganic materials. (U.S.)

  14. 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. PMID:25919128

  15. LABORATORY EVALUATION OF OIL SPILL BIOREMEDIATION PRODUCTS IN SALT AND FRESHWATER SYSTEMS

    Science.gov (United States)

    Ten oil spill bioremediation products were tested in the laboratory for their ability to enhance biodegradation of weathered Alaskan North Slope crude oil in both fresh and salt-water media. The products included: nutrients to stimulate inoculated microorganisms, nutrients plus a...

  16. Salt effect on (liquid + liquid) equilibrium of (water + tert-butanol + 1-butanol) system: Experimental data and correlation

    Energy Technology Data Exchange (ETDEWEB)

    Pereira, Milton A.P. [School of Chemical Engineering, State University of Campinas, P.O. Box 6066, Campinas-SP 13081-970 (Brazil); Aznar, Martin [School of Chemical Engineering, State University of Campinas, P.O. Box 6066, Campinas-SP 13081-970 (Brazil)]. E-mail: maznar@feq.unicamp.br

    2006-01-15

    (Liquid + liquid) equilibrium data for the quaternary systems (water + tert-butanol + 1-butanol + KBr) and (water + tert-butanol + 1-butanol + MgCl{sub 2}) were experimentally determined at T = 293.15 K and T = 313.15 K. For mixtures with KBr, the overall salt concentrations were 5 and 10 mass percent; for mixtures with MgCl{sub 2}, the overall salt concentrations were 2 and 5 mass percent. The experimental results were used to estimate molecular interaction parameters for the NRTL activity coefficient model, using the Simplex minimization method and a concentration-based objective function. The correlation results are extremely satisfactory, with deviations in phase compositions below 1.7%.

  17. Structures and interactions in aqueous solutions and gels of thermoresponsive polymer systems

    Czech Academy of Sciences Publication Activity Database

    Spěváček, Jiří

    Dharwad: Karnatak University, Department of Chemistry, 2015. s. 25. [International Conference on Direct Digital Manufacturing and Polymers - ICDDMAP 2015. 28.10.2015-31.10.2015, Dharwad] R&D Projects: GA ČR(CZ) GA15-13853S Institutional support: RVO:61389013 Keywords : thermoresponsive polymers * aqueous solution * hydrogel Subject RIV: CD - Macromolecular Chemistry

  18. Exploiting donor-acceptor interactions in aqueous dynamic combinatorial libraries : exploratory studies of simple systems

    NARCIS (Netherlands)

    Au-Yeung, Ho Yu; Cougnon, Fabien B. L.; Otto, Sijbren; Pantos, G. Dan; Sanders, Jeremy K. M.; Pantoş, G. Dan

    2010-01-01

    The behaviour of aqueous dynamic combinatorial libraries (DCLs) containing either electron-rich donor building blocks based on dioxynaphthalene (DN), or electron-deficient acceptor building blocks based on naphthalenediimide (NDI) are described. The influence of concentration and ionic strength on l

  19. Salt Tolerance

    OpenAIRE

    Xiong, Liming; Zhu, Jian-Kang

    2002-01-01

    Studying salt stress is an important means to the understanding of plant ion homeostasis and osmo-balance. Salt stress research also benefits agriculture because soil salinity significantly limits plant productivity on agricultural lands. Decades of physiological and molecular studies have generated a large body of literature regarding potential salt tolerance determinants. Recent advances in applying molecular genetic analysis and genomics tools in the model plant Arabidopsis thaliana are sh...

  20. Novel aqueous chitosan-based dispersions as efficient drug delivery systems for topical use. Rheological, textural and release studies.

    Science.gov (United States)

    Lucero, M J; Ferris, C; Sánchez-Gutiérrez, C A; Jiménez-Castellanos, M R; de-Paz, M-V

    2016-10-20

    The use of a novel cross-linked thiolated chitosan (CTS) was investigated as the main component of aqueous dispersions (at 1% and 3% w/v) for topical drug delivery systems. The nonionic theophiline (Th) and the cationic diltiazem(.)HCl (Dt) (at 0.5% w/v concentration) were used as model drugs. All aqueous dispersions behaved as viscoelastic fluids. The CTS 1% dispersions showed predominance of viscous component and low viscosity. However, in the CTS 3% dispersions, both the elastic component and high viscosities prevailed. So, texture parameters improved from CTS 1% to 3% dispersions and CTS 3%-Dt showed greater cohesion and adhesion than CTS 3%-Th, but always below CTS alone. All dispersions showed a Fickian diffusion mechanism. Despite release profiles of both drugs almost fully overlapped at 1% CTS, diffusion coefficients confirmed Dt released faster than Th at 3% CTS. The rheological behavior and the chemical nature of the drugs explained these results. PMID:27474615

  1. Evaluation of Two Biosorbents in the Removal of Metal Ions in Aqueous Using a Pilot Scale Fixed-bed System

    Directory of Open Access Journals (Sweden)

    Andre Gadelha Oliveira

    2014-05-01

    Full Text Available The aim of the present work was to investigate the adsorption of toxic metal ions copper, nickel and zinc from aqueous solutions using low cost natural biomass (sugar cane bagasse and green coconut fiber in pilot scale fixed-bed system. The Hydraulic retention time (HRT was 229 minutes and the lowest adsorbent usage rate (AUR found was 0.10 g.L-1 for copper using green coconut fibers. The highest values of adsorption capacities founded were 1.417 and 2.772 mg.g-1 of Cu(II ions for sugarcane bagasse and green coconut fibers, respectively. The results showed that both sugarcane bagasse and green coconut fiber presented potential in the removal of metal ions copper, nickel and zinc ions from aqueous solution and the possible use in wastewater treatment station.

  2. Gases in molten salts

    CERN Document Server

    Tomkins, RPT

    1991-01-01

    This volume contains tabulated collections and critical evaluations of original data for the solubility of gases in molten salts, gathered from chemical literature through to the end of 1989. Within the volume, material is arranged according to the individual gas. The gases include hydrogen halides, inert gases, oxygen, nitrogen, hydrogen, carbon dioxide, water vapor and halogens. The molten salts consist of single salts, binary mixtures and multicomponent systems. Included also, is a special section on the solubility of gases in molten silicate systems, focussing on slags and fluxes.

  3. Geomechanics of bedded salt

    International Nuclear Information System (INIS)

    Creep data from the literature search is reinterpreted by SGI, resulting in a better understanding of the temperature and stress state dependence of the octahedral creep rate and the octahedral shear strength. The concept of a transition strength between the elastic and the plastic states is in agreement with the data. The elastic and rheological properties of salt are described, and a set of constitutive equations is presented. The dependence of material properties on parameters such as temperature is considered. Findings on the permeability of salt are summarized, and the in-situ behavior of openings in bedded salt is described based on extensive engineering experience. A stress measuring system utilizing a finite element computer code is discussed. Geological factors affecting the stability of salt openings are considered, and the Stress Control Technique for designing stable openings in bedded salt formations is explained

  4. The molten salt reactors (MSR) pyro chemistry and fuel cycle for innovative nuclear systems; Congres sur les reacteurs a sels fondus (RSF) pyrochimie et cycles des combustibles nucleaires du futur

    Energy Technology Data Exchange (ETDEWEB)

    Brossard, Ph. [GEDEON, Groupement de Recherche CEA CNRS EDF FRAMATOME (France); Garzenne, C.; Mouney, H. [and others

    2002-07-01

    precipitation processes); cold salt: potentiality and preliminary results; TOPIC: redox control of MSR fuel (MSR: nominal operating conditions for the reprocessing process and redox control); technical aspects of R and D of some advanced non-aqueous reprocessing technologies for MSR systems (promising innovative separation and partitioning processes for the MSR fuel cycle); nominal operating conditions for MSR reprocessing process - data base needed and experiments for reprocessing validation; corrosion and materials for MSR and for pyro-chemistry processes; MSR reactor physics - dynamic behaviour; what safety principles for MSR? (MSR and integrated cycle (IFR) safety approach); experimental programmes in the frame of the SPHINX project of MS transmuter (programme of irradiated probes BLANKA, experimental facilities (MSR)); ISTC 1606 status - experimental study of molten salt technology for safe, low-waste and proliferation resistant treatment of radioactive waste and plutonium in accelerator-driven and critical systems. (J.S.)

  5. Basin Analysis and Petroleum System Characterization and Modeling, Interior Salt Basins, Central and Eastern Gulf of Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Ernest A. Mancini

    2005-03-31

    The principal research effort for Year 2 of the project is the determination of the burial and thermal maturation histories and basin modeling and petroleum system identification of the North Louisiana Salt Basin. In the first six (6) to nine (9) months of Year 2, the research focus is on the determination of the burial and thermal maturation histories and the remainder of the year the emphasis is on basin modeling and petroleum system identification. No major problems have been encountered to date, and the project is on schedule.

  6. BASIN ANALYSIS AND PETROLEUM SYSTEM CHARACTERIZATION AND MODELING, INTERIOR SALT BASINS, CENTRAL AND EASTERN GULF OF MEXICO

    Energy Technology Data Exchange (ETDEWEB)

    Ernest A. Mancini

    2004-11-05

    The principal research effort for Year 2 of the project is the determination of the burial and thermal maturation histories and basin modeling and petroleum system identification of the North Louisiana Salt Basin. In the first six (6) to nine (9) months of Year 2, the research focus is on the determination of the burial and thermal maturation histories and the remainder of the year the emphasis is on basin modeling and petroleum system identification. No major problems have been encountered to date, and the project is on schedule.

  7. Aqueous extraction of pumpkin seed oil by salt effect and its physicochemical properties%盐效应辅助水剂法提取南瓜籽油及其理化特性研究

    Institute of Scientific and Technical Information of China (English)

    李清华; 夏仙亦; 于修烛; 许春瑾

    2012-01-01

    摘要:为了改善水剂法提取的油乳化严重现象并且提高出油率。以南瓜籽为实验材料,碳酸钠溶液为萃取剂,采用盐效应辅助水剂法提取南瓜籽油。考察了碳酸钠浓度、液料比、提取时间、搅油温度四个因素对南瓜籽提油率的影响,并利用响应面分析对提油工艺进行了优化。结果表明,碳酸钠溶液浓度和液料比对提油率的影响较大;盐效应水剂法提取南瓜籽油在搅油温度为80℃条件下.最优工艺条件为:碳酸钠浓度1.8mol/L、液料比6.8:1(mL:g)、提取时间120.2min(实验实际提取时间选为120min),南瓜籽提油率为70.6%;南瓜籽油的酸值和过氧化值等均符合国家食用油质量标准.可以直接食用.表明盐效应辅助水剂法提取南瓜籽油工艺是可行的。%The oil was extracted from pumpkin seed by the aqueous method with sodium carbonate solvent as the extractant which aimed to overcome severe emulsification and increases the oil yield. The concentration of sodium carbonate solution,stirring temperature,liquid-solid ratio and extraction time on oil yield of pumpkin seed were investigated and the optimal parameters were carried out by Box-Behnken experimental design. The results showed that the concentration of sodium carbonate solvent and liquid-solid ratio had significant effect on the oil yield. The optimal conditions were sodium carbonate concentration 1,8mol/L,liquid-solid ratio 6.8, extraction time 120.1 min (120min in fact) ,temperature 80%,the oil yield of pumpkin seeds could reach 70.6%. The acid value and peroxide value of oil were lower than the corresponding value of the national quality standards. It demonstrated that technology for aqueous extraction of pumpkin seed oil by salt effect was workable.

  8. Modeling of 1-1-electrolyte solubility processes in ternary aqueous-organic systems using Chen's theory

    International Nuclear Information System (INIS)

    A model for the calculation of MCl electrolyte salting-out process (M = Na - Cs) in water-organic media is suggested on the basis of the Chen model for aquerous solutions of electrolytes and the Izmailov continual approximation. For the calculations made for unstudied systems the values of couple interaction parameters, obtained by the optimization of coefficients of the given electrolyte activity in water and coefficient B by the results of calculation of the given electrolyte solubility in one of the known systems, are required

  9. Successful field and laboratory tests of advanced phytoremediation systems for decontamination of petroleum and salt impacted soils

    Energy Technology Data Exchange (ETDEWEB)

    Greenberg, B.; Huang, X.D.; Gerhardt, K.; Gurska, J.; Yu, X.M.; MacNeill, G.; Lu, X.; Nykamp, J.; Glick, B.; Wang, W.; Wang, H.; Wu, S.; Knezevich, N.; Gerwing, P. [Waterloo Univ., ON (Canada)]|[Earthmaster Environmental Strategies Inc., Calgary, AB (Canada)]|[Waterloo Environmental Biotechnology Inc., Waterloo, ON (Canada)

    2008-07-01

    This presentation discussed the advantages of phytoremediation and provided an overview of a phytoremediation tests results for petroleum and salt remediation. Several examples of remediation methods were discussed, including the dig and dump method; soil incineration; chemical extraction; electrokinetic separation and land farming/natural attenuation. The advantages of phytoremediation include improved natural structure and texture of soil; suitability to most regions and climates because it is driven by solar energy; cost effectiveness and technically feasible; reasonable time frame for restoration; promotion of high rhizosphere activity by plants; and effective use at remote sites. The development and proof of plant growth promoting rhizobacteria (PGPR) enhanced phytoremediation systems (PEPS) was then addressed. A description of the PEPS was provided. This presentation also reviewed the interaction of a PGPR containing ACC deaminase with a plant seed or root; research and development of the PEPS for PHC remediation; the use of petroleum remediation on an Imperial Oil Sarnia land farm; proof of concept of the application of the PEPS for PHC remediation in Hinton, Alberta; and development of the PEPS for salt impacted sites. Field work and the characteristics of soils were also examined. It was concluded that the PEPS has great potential for efficient remediation of organic, salt and metal contaminated sites and that PGPR alleviates stress and promotes growth resulting in low ethylene and high auxin content. tabs., figs.

  10. A three-dimensional simulation of a parabolic trough solar collector system using molten salt as heat transfer fluid

    International Nuclear Information System (INIS)

    Investigations on the thermal physics mechanisms of the parabolic trough collector systems (PTCs) play a vital role in the utilization of solar energy. In this paper, a three-dimensional simulation based on Finite Element Method (FVM) is established to solve the complex problem coupling with radiation, heat conduction and convection in the PTCs. The performances of the PTCs using molten salt as the heat transfer fluid were numerically studied, and the influences of the key operating parameters on the PTCs were investigated. As a result, it can be found that the circumferential temperature difference (CTD) of the absorber increases with the rising of the direct normal irradiance (DNI) and decreases with the increase of heat transfer fluid (HTF) inlet temperature and inlet velocity. With the velocity of the molten salt in the range of 1 m/s–4 m/s, the DNIs of 500 W/m2–1250 W/m2 and the inlet temperature of 623 K–825 K, the CTD of the absorber can reach 12 K–42 K. Furthermore, the numerical results indicate the non-uniform distribution of the solar energy flux affects the CTD of receiver while has a little influence on the thermal efficiency. The promising results will provide a reference for the design of the novel parabolic trough solar collectors. - Highlights: • A coupled three-dimensional simulation is established. • The performance of the PTCs with molten salt as HTF was obtained. • The effects of key parameters on the PTCs with molten salt were achieved. • The coupling characteristics of thermal and fluid of the receiver were disclosed

  11. Granular encapsulation of light hydrophobic liquids (LHL) in LHL-salt water systems: Particle induced densification with quartz sand.

    Science.gov (United States)

    Boglaienko, Daria; Tansel, Berrin; Sukop, Michael C

    2016-02-01

    Addition of granular materials to floating crude oil slicks can be effective in capturing and densifying the floating hydrophobic phase, which settles by gravity. Interaction of light hydrophobic liquids (LHL) with quartz sand was investigated in LHL-salt water systems. The LHLs studied were decane, tetradecane, hexadecane, benzene, toluene, ethylbenzene, m-xylene, and 2-cholorotoluene. Experiments were conducted with fine quartz sand (passing sieve No. 40 with openings 0.425 mm). Each LHL was dyed with few crystals of Sudan IV dye for ease of visual observation. A volume of 0.5 mL of each LHL was added to 100 mL salt water (34 g/L). Addition of one gram of quartz sand to the floating hydrophobic liquid layer resulted in formation of sand-encapsulated globules, which settled due to increased density. All LHLs (except for a few globules of decane) formed globules covered with fine sand particles that were heavy enough to settle by gravity. The encapsulated globules were stable and retained their shape upon settling. Polarity of hydrophobic liquids as the main factor of aggregation with minerals was found to be insufficient to explain LHL aggregation with sand. Contact angle measurements were made by submerging a large quartz crystal with the LHL drop on its surface into salt water. A positive correlation was observed between the wetting angle of LHL and the LHL volume captured (r = 0.75). The dependence of the globule density on globule radius was analyzed in relation to the coverage (%) of globule surface (LHL-salt water interface) by fine quartz particles. PMID:26490430

  12. Design considerations for concentrating solar power tower systems employing molten salt.

    Energy Technology Data Exchange (ETDEWEB)

    Moore, Robert Charles; Siegel, Nathan Phillip; Kolb, Gregory J.; Vernon, Milton E.; Ho, Clifford Kuofei

    2010-09-01

    The Solar Two Project was a United States Department of Energy sponsored project operated from 1996 to 1999 to demonstrate the coupling of a solar power tower with a molten nitrate salt as a heat transfer media and for thermal storage. Over all, the Solar Two Project was very successful; however many operational challenges were encountered. In this work, the major problems encountered in operation of the Solar Two facility were evaluated and alternative technologies identified for use in a future solar power tower operating with a steam Rankine power cycle. Many of the major problems encountered can be addressed with new technologies that were not available a decade ago. These new technologies include better thermal insulation, analytical equipment, pumps and values specifically designed for molten nitrate salts, and gaskets resistant to thermal cycling and advanced equipment designs.

  13. Kinetics of carbonate dissolution in CO2-saturated aqueous system at reservoir conditions

    Science.gov (United States)

    Peng, Cheng; Crawshaw, John P.; Maitland, Geoffrey; Trusler, J. P. Martin

    2014-05-01

    In recent years, carbon capture and storage (CCS) has emerged as a key technology for limiting anthropogenic CO2 emissions while allowing the continued utilisation of fossil fuels. The most promising geological storage sites are deep saline aquifers because the capacity, integrity and injection economics are most favourable, and the environmental impact can be minimal. Many rock-fluid chemical reactions are known to occur both during and after CO2 injection in saline aquifers. The importance of rock-fluid reactions in the (CO2 + H2O) system can be understood in terms of their impact on the integrity and stability of both the formation rocks and cap rocks. The chemical interactions between CO2-acidified brines and the reservoir minerals can influence the porosity and permeability of the formations, resulting in changes in the transport processes occurring during CO2 storage. Since carbonate minerals are abundant in sedimentary rocks, one of the requirements to safely implement CO2 storage in saline aquifers is to characterise the reactivity of carbonate minerals in aqueous solutions at reservoir conditions. In this work, we reported measurements of the intrinsic rate of carbonate dissolution in CO2-saturated water under high-temperature high-pressure reservoir conditions extending up to 373 K and 14 MPa. The rate of carbonate dissolution in CO2-free HCl(aq) was also measured at ambient pressure at temperatures up to 353 K. Various pure minerals and reservoir rocks were investigated in this study, including single-crystals of calcite and magnesite, and samples of dolomite, chalks and sandstones. A specially-designed batch reactor system, implementing the rotating disc technique, was used to obtain the intrinsic reaction rate at the solid/liquid interface, free of mass transfer effects. The effective area and mineralogy of the exposed surface was determined by a combination of surface characterisation techniques including XRD, SEM, EDX and optical microscopy. The

  14. Design and development of single stage purification of papain using Ionic Liquid based aqueous two phase extraction system and its Partition coefficient studies

    OpenAIRE

    Senthilkumar Rathnasamy; R.Kumaresan2

    2013-01-01

    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 ma...

  15. Investigation of heterogenous equilibria in uranoborate MII(BUO5)2·nH2O - aqueous solution system (MII=Mn, Co, Ni, Zn)

    International Nuclear Information System (INIS)

    State of uranoborates of MII(BUO5)2·nH2O (MII=Mn, Co, Ni, Zn) series in aqueous solutions of inorganic acid at 25 Deg C is investigated. Using experimental data on uranoborate solubility in hydrochloric acid a quantitative model of the system uranoborate - aqueous solution is proposed. The model is used for forecasting of states of heterogenous systems in different conditions and for calculation of standard thermodynamic functions of uranoborates

  16. Impact of salt stress on the features and activities of root system for three desert halophyte species in their seedling stage

    Institute of Scientific and Technical Information of China (English)

    YI LiangPeng; MA Jian; LI Yan

    2007-01-01

    Linkage between belowground and aboveground sections of ecological system is mainly depending on root system. But root system is the parts of plant that people less understand. The absorption function of root system is closely related to their morphology and activity. Moreover root system can interact with the environmental stress under the adverse situation, and adjust its system to take adaptation responses in morphology and physiology to strengthen its survival chance. This research is focused on three desert halophyte species of H. ammodendron (C.A.Mey.) Bge., S. physophora Pall., and S.nitraria Pall. under solution culture, to study the differences of their root system morphology and activity in the seedling stage under varying salt concentration conditions. The study results show that: A certain salt concentration can promote development of these three halophytes; but rather high salt concentration will restrain their growth, in particular inhibit the root system development. Under the same salt concentration condition, S. nitraria Pall. grows fast and accumulates the largest amount of biomass. Under relatively low salt concentration, the length of axial root and the total length of root system of these three halophyte species are all increased; and compared to the checking samples, S.physophora Pall. occupies the top place of root system growth, but the high salt concentration will restrain the increase of total root length; among them, the impact intensity on S. physophora Pall. is lighter than to H. ammodendron (C.A.Mey.) Bge. and S. nitraria Pall. is lighter; the salinity does not bring distinct influence on the average diameter of root system of these three plant species, but trends to reducing the size; under the solution culture conditions, the middle and lower parts of the axial root of H. ammodendron (C.A.Mey.) Bge. and S. physophora Pall. are rather equally distributed, but the central zone of S. nitraria Pall. root system is more significantly

  17. Pectinases partitioning in aqueous two-phase systems: an integration of the systems poly(ethylene glycol/crude dextran and poly(ethylene glycol/ammonium sulphate

    Directory of Open Access Journals (Sweden)

    STANA N. PEJIN

    2004-04-01

    Full Text Available The partitioning of pectinases in the poly(ethylene glucol4000/ammonium sulpohate system was studied and also its application for enzymes extraction from the top phase of the poly(ethylene glucol4000/crude dextran system. Almost complete one-sided partition of endo-pectinase and exo-pectinase to the bottom phase of the polymer/salt system was achieved at a tie-line length of 37.16 %. The concentration factors were 1.73 and 3.25, respectively. The highest total endo- and exo-pectinase yields (72.41 % and 69.46 %, respectively were obtained by integration of the polymer/polymer system at a tie-line of 8.61 % and a high phase volume ratio and the polymer/salt system at a tie-line of 30.23 % and a low phase volume ratio. Integration of the partitioning at a high tie-line length in the polymer/polimer and a low tie-line length in the polymer/salt system resulted in a total concentration factor of 1.5 and a purification of 1.66 fold for exo-pectinase. The addition of phosphate to this integrated system improved the total concentration factor and purification fold of the activity to 1.73 and 2.14, respectively.

  18. Supra-molecular Association and Polymorphic Behaviour In Systems Containing Bile Acid Salts

    OpenAIRE

    Camillo La Mesa; Patrizia Andreozzi; Marco Calabresi

    2007-01-01

    A wide number of supra-molecular association modes are observed in mixtures containing water and bile salts, BS, (with, eventually, other components). Molecular or micellar solutions transform into hydrated solids, fibres, lyotropic liquid crystals and/or gels by raising the concentration, the temperature, adding electrolytes, surfactants, lipids and proteins. Amorphous or ordered phases may be formed accordingly. The forces responsible for this very rich polymorphism presumably arise from th...

  19. Modeling of aqueous and organic phase speciation for solvent extraction systems

    International Nuclear Information System (INIS)

    The TRUEX (TRansUranic EXtraction) solvent extraction process has the ability to remove, separate, and recover transuranic (TRU) elements from acidic nuclear waste solutions. A computer model of the TRUEX process is currently being developed for use in flowsheet design and process optimization. The correlations that are to be used in the model for generating extraction distribution ratios are based on chemical mass action principles and require calculation of aqueous and organic phase speciation. Aqueous phase activity coefficients are calculated using methods available in the literature, while the organic phase species are treated in terms of ideal associated solution theory. This approach is demonstrated for the extraction of HNO3, HTcO4, and americium nitrate by n-octyl(phenyl)-N,N-diisobutylcarbamoyl-methylphosphine oxide (CMPO)---the primary metal extractant in the TRUEX solvent. 23 refs., 5 figs

  20. Theoretical Studies of Aqueous Systems above 25 deg C. 1. Fundamental Concepts for Equilibrium Diagrams and some General Features of the Water System

    International Nuclear Information System (INIS)

    The illustration of thermodynamic data on aqueous systems is discussed and diagrams are described that are useful for bringing together the large numbers of data that are relevant to technological problems such as corrosion, mass-transport and deposition. Two kinds of logarithmic equilibrium diagram are particularly useful, namely, diagrams depicting the variation with pH or pe of the concentrations of ionic species relative to that of a chosen reference ion and diagrams depicting the fields of conditions of pH and pe in which the various species in any given system predominate or are stable. Such diagrams clearly and concisely illustrate the data and greatly simplify the comparison of the states of a system at different temperatures. Estimates of the equilibrium constants for the redox and the acid-base dissociation of water up to 375 C are reported and some general features of aqueous systems at elevated temperatures are discussed

  1. The decomposition yields and reactivity of metal tetrasulfophthalocyanines in aqueous-alcohol system

    International Nuclear Information System (INIS)

    The effect of gamma radiation on metal (Rh, Mn, Co, Ni and Cu) tetrasulfophthalocyanines in aqueous and water:methanol solutions have been studied. The determined yields of the complex decomposition (measured on the basis of absorption decays) decrease with the increase of the dose and depend on the composition of the matrix. The rate constants of radical scavenging have been determined applying the competition method with p-nitrosodimethylaniline

  2. Temperature-induced phase transition in aqueous solutions and gels of multicomponent polymer systems

    Czech Academy of Sciences Publication Activity Database

    Spěváček, Jiří; Konefal, Rafal; Dybal, Jiří

    Kolkata : Indian Association for the Cultivation of Science, 2016. s. 48-49. [International IUPAC Conference on Polymer -Solvent Complexes and Intercalates /11./ - POLYSOLVAT-11. 27.01.2016-30.01.2016, Kolkata] R&D Projects: GA ČR(CZ) GA15-13853S Institutional support: RVO:61389013 Keywords : temperature-induced phase transition * aqueous solution * hydrogel Subject RIV: CD - Macromolecular Chemistry

  3. On-line measurements of UV-VIS spectra in high-temperature molten salt media : development of measuring systems

    International Nuclear Information System (INIS)

    Recently, ionic melts have become attractive reaction media in many fields. Molten salt based electrochemical processes have been proposed as a promising method for future nuclear programs and more specifically for spent fuel processing. Molten alkaline chloride based melts are considered as a promising reaction media. For this, it is interesting to understand the chemical nature of the actinides and lanthanides in high-temperature melt. Some spectroscopy provides essential information on the exact nature of f-block elements LiCl-KCl melt system. High temperature electronic absorption spectroscopy challenges researchers to design and build specific apparatus/equipment and maintain certain strict physicochemical conditions. First of all, to reach to that goal, it is necessary to setup special apparatus and measuring equipment. Here, we report the details of the design of the reaction system combined with the instrumentation of the spectrometer system. Also, application result of the measuring system to U(III) involved chemical reaction in molten salt media was introduced

  4. Partition of synaptic membranes in aqueous two-phase systems at subzero temperatures by using anti-freeze solvent.

    Science.gov (United States)

    Johansson, G; Joelsson, M; Olde, B

    1990-11-16

    The freezing point of aqueous two-phase (liquid-liquid) systems containing water, dextran and poly(ethylene glycol) has been lowered by including glycerol. Biological membranes, obtained by fragmentation of a crude synaptosomal preparation from calf brain cortex, have been included in the two-phase systems. The effects of temperature and the concentration of glycerol on the partition of the membranes within the systems have been investigated. Considerable stabilisation of the membranes was noticed when they were partitioned at -10 degrees C compared with 0 degrees C. The influences of glycerol, ethylene glycol, N,N-dimethylformamide and tetrahydrofuran on the phase-forming properties of the systems and on enzyme activities are also presented. Possible use of the above systems for studies and separation of biological membranes are discussed. PMID:2245213

  5. Pencil lead scratches on steel surfaces as a substrate for LIBS analysis of dissolved salts in liquids

    Energy Technology Data Exchange (ETDEWEB)

    Jijon, D; Costa, C, E-mail: judijival@hotmail.com [Departamento de Fisica, Escuela Politecnica Nacional, Ladron de Guevara E11-256, Apartado 17-12-866, Quito (Ecuador)

    2011-01-01

    A new substrate for the quantitative analysis of salts dissolved in liquids with Laser-induced Breakdown Spectroscopy (LIBS) is introduced for the first time. A steel surface scratched with HB pencil lead is introduced as a very efficient and sensitive substrate for quantitative analysis of dissolved salts in liquids. In this work we demonstrate the analytical quality of this system with the analysis of the crystalline deposits formed by the dried aqueous solutions of salts. We focused on analytical parameters such as sensitivity and linearity for the salt cations in each case. Four salts were studied (Sr(NO{sub 3}){sub 2}, LiSO{sub 4}, RbCl and BaCl), at nine different concentrations each. To improve linearity and lower the overall error in the calibration curves, we introduce a novel outlier removal method that takes into account the homogeneity of the dry deposits on the analytical surface.

  6. Pencil lead scratches on steel surfaces as a substrate for LIBS analysis of dissolved salts in liquids

    International Nuclear Information System (INIS)

    A new substrate for the quantitative analysis of salts dissolved in liquids with Laser-induced Breakdown Spectroscopy (LIBS) is introduced for the first time. A steel surface scratched with HB pencil lead is introduced as a very efficient and sensitive substrate for quantitative analysis of dissolved salts in liquids. In this work we demonstrate the analytical quality of this system with the analysis of the crystalline deposits formed by the dried aqueous solutions of salts. We focused on analytical parameters such as sensitivity and linearity for the salt cations in each case. Four salts were studied (Sr(NO3)2, LiSO4, RbCl and BaCl), at nine different concentrations each. To improve linearity and lower the overall error in the calibration curves, we introduce a novel outlier removal method that takes into account the homogeneity of the dry deposits on the analytical surface.

  7. A comparison of the coupled fresh water-salt water flow and the Ghyben-Herzberg sharp interface approaches to modeling of transient behavior in coastal aquifer systems

    Science.gov (United States)

    Essaid, H.I.

    1986-01-01

    A quasi-three dimensional finite difference model which simulates coupled, fresh water and salt water flow, separated by a sharp interface, is used to investigate the effects of storage characteristics, transmissivity, boundary conditions and anisotropy on the transient responses of such flow systems. The magnitude and duration of the departure of aquifer response from the behavior predicted using the Ghyben-Herzberg, one-fluid approach is a function of the ease with which flow can be induced in the salt water region. In many common hydrogeologic settings short-term fresh water head responses, and transitional responses between short-term and long-term, can only be realistically reproduced by including the effects of salt water flow on the dynamics of coastal flow systems. The coupled fresh water-salt water flow modeling approach is able to reproduce the observed annual fresh water head response of the Waialae aquifer of southeastern Oahu, Hawaii. ?? 1986.

  8. Design of Complex Systems to Achieve Passive Safety: Natural Circulation Cooling of Liquid Salt Pebble Bed Reactors

    Science.gov (United States)

    Scarlat, Raluca Olga

    This dissertation treats system design, modeling of transient system response, and characterization of individual phenomena and demonstrates a framework for integration of these three activities early in the design process of a complex engineered system. A system analysis framework for prioritization of experiments, modeling, and development of detailed design is proposed. Two fundamental topics in thermal-hydraulics are discussed, which illustrate the integration of modeling and experimentation with nuclear reactor design and safety analysis: thermal-hydraulic modeling of heat generating pebble bed cores, and scaled experiments for natural circulation heat removal with Boussinesq liquids. The case studies used in this dissertation are derived from the design and safety analysis of a pebble bed fluoride salt cooled high temperature nuclear reactor (PB-FHR), currently under development in the United States at the university and national laboratories level. In the context of the phenomena identification and ranking table (PIRT) methodology, new tools and approaches are proposed and demonstrated here, which are specifically relevant to technology in the early stages of development, and to analysis of passive safety features. A system decomposition approach is proposed. Definition of system functional requirements complements identification and compilation of the current knowledge base for the behavior of the system. Two new graphical tools are developed for ranking of phenomena importance: a phenomena ranking map, and a phenomena identification and ranking matrix (PIRM). The functional requirements established through this methodology were used for the design and optimization of the reactor core, and for the transient analysis and design of the passive natural circulation driven decay heat removal system for the PB-FHR. A numerical modeling approach for heat-generating porous media, with multi-dimensional fluid flow is presented. The application of this modeling

  9. Salts and Co-crystals of Theobromine and their phase transformations in water

    Indian Academy of Sciences (India)

    Palash Sanphui; Ashwini Nangia

    2014-09-01

    Theobromine, a xanthine derivative analogous to caffeine and theophylline, is an effective central nervous system stimulant. It has lower aqueous solubility than caffeine and theophylline. Salts of theobromine with hydrochloric acid, phosphoric acid, methanesulfonic acid, benzenesulfonic acid and -toluenesulfonic acid were prepared using liquid-assisted grinding (LAG). Proton transfer from the strong acid to the weak base imidazole N resulted in N+-H…O− hydrogen-bonded supramolecular assemblies of theobromine salts. The mesylate salt is polymorphic with amide N-H…O dimer and catemer synthons for the theobromine cations. A variable stoichiometry for phosphate salts (1:3 and 1:2.5) were observed with the latter being more stable. All new salts were characterized by FT-IR, PXRD, DSC and finally single crystal X-ray diffraction. In terms of stability, these salts transformed to theobromine within 1 h of dissolution in water. Remarkably, the besylate and tosylate salts are 88 and 58 times more soluble than theobromine, but they dissociated within 1 h. In contrast, theobromine co-crystals with gallic acid, anthranilic acid and 5-chlorosalicylic acid were found to be stable for more than 24 h in the aqueous slurry conditions, except malonic co-crystal which transformed to theobrominewithin 1 h.Water mediated phase transformation of theobromine salts and co-crystalmay be due to the incongruency (high solubility difference) between the components. These results suggest that even though traditional salts are highly soluble compared to co-crystals, co-crystals can be superior in terms of stability.

  10. Extraction and Purification of Quercitrin, Hyperoside, Rutin, and Afzelin from Zanthoxylum Bungeanum Maxim Leaves Using an Aqueous Two-Phase System.

    Science.gov (United States)

    He, Fengyuan; Li, Dengwu; Wang, Dongmei; Deng, Ming

    2016-07-01

    In this study, an aqueous two-phase system (ATPS) based on ethanol/NaH2 PO4 was developed for the extraction and purification of quercitrin, hyperoside, rutin, and afzelin from Zanthoxylum bungeanum Maxim leaves. These 4 flavonoids were 1st extracted from dried Z. bungeanum leaves using a 60% ethanol solution and subsequently added to the ATPS for further purification. The partition behavior of the 4 flavonoids in ATPS was investigated. The optimal ATPS conditions were: 29% (w/w) NaH2 PO4 , 25% (w/w) ethanol concentration, 1% (w/w) added amount of leaf extracts, no pH adjustment, and repeated 1 h extractions at 25 °C. Under the optimal conditions for the 10 g ATPS, the absolute recovery of quercitrin, hyperoside, rutin, and afzelin reached 90.3%, 83.5%, 92.3%, and 89.1%, respectively. Compared to the 60% ethanol extracts, the content of quercitrin (44.8 mg/g), hyperoside (65.6 mg/g), rutin (56.4 mg/g), and afzelin (6.84 mg/g) in the extracts increased by 49.9%, 38.8%, 45.6%, and 36.8% respectively. The extracts after ATPS also exhibited stronger antioxidant activities, the 2,2-diphenyl-1-picrylhydrazyl IC50 value (10.5 μg/mL) decreased by 41.8%, and the 2,2-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt value (966 μmol Trolox/g) and ferric reducing power value (619 μmol Trolox/g) increased by 29.8% and 53.7%, respectively. Furthermore, scale-up experiments indicated that a larger scale experiment was feasible for the purification of the 4 flavonoids. PMID:27240023

  11. Investigation of heterogeneous equilibria in the system uranosilicate MHSiUO6·nH2O - aqueous solvent (M=Li, Na, K)

    International Nuclear Information System (INIS)

    State of mineral-like compounds of MHSiUO6·nH2O (M=Li, Na, K) composition in aqueous solutions at 298 K is investigated. Taking experimental data on solubility as a basis quantitative model of the system crystalline uranosilicate - aqueous solution is proposed. This model could be a basis for calculation of Gibbs formation functions and solubility product. Gibbs formation functions of silicic acid and other ionic-molecular forms of existence of Si(IV) in solution are calculated. Using the proposed model solubility of uranosilicates in aqueous solutions (in the region, which are not investigated experimentally) is forecasted

  12. Electrolytic orthoborate salts for lithium batteries

    Science.gov (United States)

    Angell, Charles Austen; Xu, Wu

    2008-01-01

    Orthoborate salts suitable for use as electrolytes in lithium batteries and methods for making the electrolyte salts are provided. The electrolytic salts have one of the formulae (I). In this formula anionic orthoborate groups are capped with two bidentate chelating groups, Y1 and Y2. Certain preferred chelating groups are dibasic acid residues, most preferably oxalyl, malonyl and succinyl, disulfonic acid residues, sulfoacetic acid residues and halo-substituted alkylenes. The salts are soluble in non-aqueous solvents and polymeric gels and are useful components of lithium batteries in electrochemical devices.

  13. Measuring and modeling aqueous electrolyte/amino-acid solutions with ePC-SAFT

    International Nuclear Information System (INIS)

    Highlights: • Amino-acid solubilities and osmotic coefficients in ternary solutions containing one amino acids and one salt measured. • Weak salt influence on amino-acid solubilities except for salts containing Mg[2+] or NO3[−] (salting-in behavior). • Osmotic coefficients dominated by the solute with the highest molality. • Amino-acid solubilities and osmotic coefficients predicted reasonably with ePC-SAFT with deviations of 3.7% and 9.3%. • Predictions based on pure-component parameters for ions and amino acids using no ion/amino-acid fitting parameters. -- Abstract: In this work thermodynamic properties of electrolyte/amino acid/water solutions were measured and modeled. Osmotic coefficients at 298.15 K were measured by means of vapor-pressure osmometry. Amino-acid solubility at 298.15 K was determined gravimetrically. Considered aqueous systems contained one of the four amino acids: glycine, L-/DL-alanine, L-/DL-valine, and L-proline up to the respective amino-acid solubility limit and one of 13 salts composed of the ions Li+, Na+, K+, NH4+, Cl−, Br−, I−, NO3−, and SO42− at salt molalities of 0.5, 1.0, and 3.0 mol · kg−1, respectively. The data show that the salt influence is more pronounced on osmotic coefficients than on amino-acid solubility. The electrolyte Perturbed-Chain Statistical Association Theory (ePC-SAFT) was applied to model thermodynamic properties in aqueous electrolyte/amino-acid solutions. In previous works, this model had been applied to binary salt/water and binary amino acid/water systems. Without fitting any additional parameters, osmotic coefficients and amino-acid solubility in the ternary electrolyte/amino acid/water systems could be predicted with overall deviations of 3.7% and 9.3%, respectively, compared to the experimental data

  14. Modulating the Solubilities of Ionic Liquid Components in Aqueous-Ionic Liquid Biphasic Systems: A Q-NMR Investigation.

    Science.gov (United States)

    Atanassova, Maria; Mazan, Valérie; Billard, Isabelle

    2015-06-01

    Aqueous-ionic liquid (A-IL) biphasic systems have been examined in terms of deuterated water, acid, and IL cation and anion mutual solubilities in the upper (water-rich, in mole fraction) and lower phase of aqueous/IL biphasic systems at ambient temperature. The biphasic mixtures were composed of deuterated acids of various concentrations (mainly DCl, DNO(3), and DClO(4) from 10(-2) to 10(-4)  M) and five ionic liquids of the imidazolium family with a hydrophobic anion (CF(3)SO(2))(2) N(-), that is, [C1 Cn im][Tf(2)N], (n=2, 4, 6, 8 and 10). The analytical techniques applied were (1) H NMR, (19) F NMR, Karl-Fischer titration, pH potentiometry for IL cations and anions, and water and acid determination. The effects of the ionic strength (μ=0.1 M NaCl and NaNO(3) as well as μ=0.1 M, 0.2 M and 0.4 M NaClO(4), according to the investigated acid), the nature of the IL cation, and the nature of the mineral acid on the solubilities of the (D(2)O, D(+), Tf(2)N(-), C1 Cn im(+)) entities in the lower or upper phases were determined. The addition of sodium perchlorate was found to enhance the Tf(2)N(-) solubility while inhibiting the solubility of the ionic liquid cation. Differences in IL cation and anion solubilities of up to 42 mM were evidenced. The consequences for the characterization of the aqueous biphasic system, the solvent extraction process of the metal ions, and the ecological impact of the ILs are discussed. PMID:25787248

  15. Mononuclear phagocyte system depletion blocks interstitial tonicity-responsive enhancer binding protein/vascular endothelial growth factor C expression and induces salt-sensitive hypertension in rats.

    Science.gov (United States)

    Machnik, Agnes; Dahlmann, Anke; Kopp, Christoph; Goss, Jennifer; Wagner, Hubertus; van Rooijen, Nico; Eckardt, Kai-Uwe; Müller, Dominik N; Park, Joon-Keun; Luft, Friedrich C; Kerjaschki, Dontscho; Titze, Jens

    2010-03-01

    We showed recently that mononuclear phagocyte system (MPS) cells provide a buffering mechanism for salt-sensitive hypertension by driving interstitial lymphangiogenesis, modulating interstitial Na(+) clearance, and increasing endothelial NO synthase protein expression in response to very high dietary salt via a tonicity-responsive enhancer binding protein/vascular endothelial growth factor C regulatory mechanism. We now tested whether isotonic saline and deoxycorticosterone acetate (DOCA)-salt treatment leads to a similar regulatory response in Sprague-Dawley rats. Male rats were fed a low-salt diet and received tap water (low-salt diet LSD), 1.0% saline (high-salt diet HSD), or DOCA+1.0% saline (DOCA-HSD). To test the regulatory role of interstitial MPS cells, we further depleted MPS cells with clodronate liposomes. HSD and DOCA-HSD led to Na(+) accumulation in the skin, MPS-driven tonicity-responsive enhancer binding protein/vascular endothelial growth factor C-mediated hyperplasia of interstitial lymph capillaries, and increased endothelial NO synthase protein expression in skin interstitium. Clodronate liposome MPS cell depletion blocked MPS infiltration in the skin interstitium, resulting in unchanged tonicity-responsive enhance binding protein/vascular endothelial growth factor C levels and absent hyperplasia of the lymph capillary network. Moreover, no increased skin endothelial NO synthase protein expression occurred in either clodronate liposome-treated HSD or DOCA-salt rats. Thus, absence of the MPS-cell regulatory response converted a salt-resistant blood-pressure state to a salt-sensitive state in HSD rats. Furthermore, salt-sensitive hypertension in DOCA-salt rats was aggravated. We conclude that MPS cells act as onsite controllers of interstitial volume and blood pressure homeostasis, providing a local regulatory salt-sensitive tonicity-responsive enhancer binding protein/vascular endothelial growth factor C-mediated mechanism in the skin to maintain

  16. Method and system to reclaim functional sites on a sorbent contaminated by heat stable salts

    Science.gov (United States)

    Krutka, Holly; Sjostrom, Sharon; Morris, William J.

    2016-03-08

    The objective of this invention is to develop a method to reclaim functional sites on a CO.sub.2 sorbent that have reacted with an acid gas (other than CO.sub.2) to form heat stable salts (HSS). HSS are a significant concern for dry sorbent based CO.sub.2 capture because over time the buildup of HSS will reduce the overall functionality of the CO.sub.2 sorbent. A chemical treatment can remove the non-CO.sub.2 acid gas and reclaim functional sites that can then be used for further CO.sub.2 adsorption.

  17. Recent Results of the Investigation of a Microfluidic Sampling Chip and Sampling System for Hot Cell Aqueous Processing Streams

    Energy Technology Data Exchange (ETDEWEB)

    Julia Tripp; Jack Law; Tara Smith

    2013-10-01

    A Fuel Cycle Research and Development project has investigated an innovative sampling method that could evolve into the next generation sampling and analysis system for metallic elements present in aqueous processing streams. Initially sampling technologies were evaluated and microfluidics sampling chip technology was selected and tested. A conceptual design for a fully automated microcapillary-based system was completed and a robotic automated sampling system was fabricated. The mechanical and sampling operation of the completed sampling system was investigated. In addition, the production of a less expensive, mass produced sampling chip was investigated to avoid chip reuse thus increasing sampling reproducibility/accuracy. The microfluidic-based robotic sampling system’s mechanical elements were tested to ensure analytical reproducibility and the optimum robotic handling of microfluidic sampling chips.

  18. Early solar system aqueous activity - Sr isotope evidence from the Orgueil CI meteorite

    Science.gov (United States)

    Macdougall, J. D.; Lugmair, G. W.; Kerridge, J. F.

    1984-01-01

    The Sr isotopic composition and Rb-87/Sr-86 ratio have been measured in carbonates and sulfate separated from the Orgueil meteorite in order to determine the time when liquid water may have acted on the parent body. Both of the studied phases probably precipitated from aqueous solution. The results show that carbonate deposition occurred contemporaneously with parent body formation or shortly after it, probably within 100 Myr. On the other hand, at least some of the calcium sulfate seems to have been formed recently.

  19. Potential of Rice Husk and Rice Husk Ash for Phenol Removal in Aqueous Systems

    OpenAIRE

    A.H Mahvi; Maleki, A.; A. Eslami

    2004-01-01

    The potential of rice husk and rice husk ash for phenol adsorption from aqueous solution was studied. Batch kinetics and isotherm studies were carried out under varying experimental conditions of contact time, phenol concentration, adsorbent dose and pH. Adsorption equilibrium of rice husk and rice husk ash was reached within 6 hours for phenolic concentration 150-500 μg/L and 3 hours for phenol concentration 500-1300 μg/L, respectively. Kinetics of adsorption obeyed a first-order rate equa...

  20. Immobilization of lipase on sepabeads and its application in pentyl octanoate synthesis in a low aqueous system

    Directory of Open Access Journals (Sweden)

    Knežević-Jugović Zorica D.

    2008-01-01

    Full Text Available The object of the study was to investigate the process conditions relevant for the pentyl octanoate production with the lipase from Candida rugosa immobilized on Sepabeads EC-EP carrier. This is an epoxide-containing commercial polymethacrylic carrier with suitable characteristics for enzyme immobilization. The immobilized lipase suitable for pentyl octanoate synthesis has been prepared by a direct lipase binding to polymers via their epoxide groups. The enzymatic activity was determined by both hydrolysis of olive oil in an aqueous system and esterification of n-pentanol with octanoic acid in a low aqueous system. The influence of several important reaction parameters such as temperature, initial water content, initial substrate molar ratio, enzyme loading and time of adding of molecular sieves in the system is carefully analyzed by means of an experimental design. Production of the ester was optimized and an ester production response equation was obtained, making it possible to predict ester yields from known values of the five main factors. Almost complete conversion (>99% of the substrate to ester could be realized, using lipase loading as low as 37 mg/g dry support and in a relatively short time (24 h at 45ºC, when high initial substrate molar ratio of 2.2 is used.

  1. Technology demonstration: geostatistical and hydrologic analysis of salt areas. Assessment of effectiveness of geologic isolation systems

    International Nuclear Information System (INIS)

    The Office of Nuclear Waste Isolation (ONWI) requested Pacific Northwest Laboratory (PNL) to: (1) use geostatistical analyses to evaluate the adequacy of hydrologic data from three salt regions, each of which contains a potential nuclear waste repository site; and (2) demonstrate a methodology that allows quantification of the value of additional data collection. The three regions examined are the Paradox Basin in Utah, the Permian Basin in Texas, and the Mississippi Study Area. Additional and new data became available to ONWI during and following these analyses; therefore, this report must be considered a methodology demonstration here would apply as illustrated had the complete data sets been available. A combination of geostatistical and hydrologic analyses was used for this demonstration. Geostatistical analyses provided an optimal estimate of the potentiometric surface from the available data, a measure of the uncertainty of that estimate, and a means for selecting and evaluating the location of future data. The hydrologic analyses included the calculation of transmissivities, flow paths, travel times, and ground-water flow rates from hypothetical repository sites. Simulation techniques were used to evaluate the effect of optimally located future data on the potentiometric surface, flow lines, travel times, and flow rates. Data availability, quality, quantity, and conformance with model assumptions differed in each of the salt areas. Report highlights for the three locations are given

  2. Phosphate salts

    Science.gov (United States)

    ... levels that are too high, and for preventing kidney stones. They are also taken for treating osteomalacia (often ... But intravenous phosphate salts should not be used. Kidney stones (nephrolithiasis). Taking potassium phosphate by mouth might help ...

  3. Electrochemical behaviours of lanthanide fluorides in the electrolysis system with LiF-NaF-Kf salt

    International Nuclear Information System (INIS)

    As a part of partitioning studies, the experiments of cyclic voltammetry and electrolytic reduction with the liquid bismuth cathode were conducted to investigate electrochemical behaviours of lanthanide elements in the electrorefining system employing LiF-NaF-KF eutectic salt as the electrolyte. The cyclic voltammograms for NdF3 and GdF3 were obtained at various potential scan rates, respectively. The cathodic and anodic peak currents of the elements increased in proportion to the square root of the potential scan rate. According to changes of the potential difference between the coupled cathodic and anodic peaks, reversibilities of the reduction-oxidation reactions in this system were evaluated. In addition, further behaviours of electrochemical reaction of the elements were examined through electrolytic tests of the system using liquid bismuth as the cathode at fixed current densities. (author)

  4. Molecular dynamics simulations on aqueous two-phase systems - Single PEG-molecules in solution

    Directory of Open Access Journals (Sweden)

    Oelmeier Stefan A

    2012-08-01

    Full Text Available Abstract Background Molecular Dynamics (MD simulations are a promising tool to generate molecular understanding of processes related to the purification of proteins. Polyethylene glycols (PEG of various length are commonly used in the production and purification of proteins. The molecular mechanisms behind PEG driven precipitation, aqueous two-phase formation or the effects of PEGylation are however still poorly understood. Results In this paper, we ran MD simulations of single PEG molecules of variable length in explicitly simulated water. The resulting structures are in good agreement with experimentally determined 3D structures of PEG. The increase in surface hydrophobicity of PEG of longer chain length could be explained on an atomic scale. PEG-water interactions as well as aqueous two-phase formation in the presence of PO4 were found to be correlated to PEG surface hydrophobicity. Conclusions We were able to show that the taken MD simulation approach is capable of generating both structural data as well as molecule descriptors in agreement with experimental data. Thus, we are confident of having a good in silico representation of PEG.

  5. Central nervous system activity of an aqueous acetonic extract of Ficus carica L. in mice

    Directory of Open Access Journals (Sweden)

    Mittal M Bhanushali

    2014-01-01

    Full Text Available Background: Ficus carica Linn. is reported to possess variety of activities, but its potential in CNS disorders is still to be explored. Objective: The present study was carried out to evaluate the CNS depressant activity of aqueous acetonic extract of Ficus carica Linn on different models in mice. Materials and Methods: The aerial parts of the plant Ficus carica L. were extracted with aqueous acetone and the solvent was removed by rotary vacuum evaporator under reduced pressure. A crude extract was given orally and its effects were tested on ketamine-induced sleeping time, muscle-coordination, anxiety (elevated-plus maze and Staircase test, convulsions [maximal electroshock (MES and pentylenetetrazole (PTZ-induced seizures], and nociception. In addition, we determined the levels of neurotransmitters, norepinephrine (NE and 5-hydroxytryptamine (5-HT. Results: Results from the experimental models tested showed: (1 a delay on onset and prolongation of sleep of ketamine-induced sleeping time; (2 significant muscle relaxant activity; (3 a significant attenuation in the anxiety-response (4 a delay in the onset of seizures and reduction in duration of seizures and mortality induced by MES and PTZ; (5 a reduction in the licking time in nociception test and (6 increased levels of NE and 5-HT. Conclusion: This suggests that Ficus carica L. exerts its CNS depressive effect by modulating the neurotransmitters NE and 5-HT in the brain.

  6. The atomic level journey from aqueous polyoxometalate to metal oxide

    Energy Technology Data Exchange (ETDEWEB)

    Hou, Yu; Fast, Dylan B.; Ruther, Rose E.; Amador, Jenn M.; Fullmer, Lauren B.; Decker, Shawn R.; Zakharov, Lev N.; Dolgos, Michelle R., E-mail: Michelle.Dolgos@oregonstate.edu; Nyman, May, E-mail: May.Nyman@oregonstate.edu

    2015-01-15

    Aqueous precursors tailored for the deposition of thin film materials are desirable for sustainable, simple, low energy production of advanced materials. Yet the simple practice of using aqueous precursors is complicated by the multitude of interactions that occur between ions and water during dehydration. Here we use lithium polyoxoniobate salts to investigate the fundamental interactions in the transition from precursor cluster to oxide film. Small-angle X-ray scattering of solutions, total X-ray scattering of intermediate gels, and morphological and structural characterization of the lithium niobate thin films reveal the atomic level transitions between these states. The studies show that (1) lithium–[H{sub 2}Nb{sub 6}O{sub 19}]{sup 6−} has drastically different solution behaviour than lithium–[Nb{sub 6}O{sub 19}]{sup 8−}, linked to the precursor salt structure (2) in both compositions, the intermediate gel preserves the polyoxoniobate clusters and show similar local order and (3) the morphology and phases of deposited films reflect the ions behaviour throughout the journey from cluster solution to metal oxide. - Graphical abstract: Aqueous lithium polyoxoniobate salts were used to prepare lithium niobate (LiNbO{sub 3}) thin films. Fundamental studies were performed to investigate the interactions in the transition from precursor cluster to the oxide film. It was found that acid–base and ion-association chemistries of the aqueous and gel systems significantly affect the key processes in this atom-level journey. - Highlights: • Lithium polyoxoniobate clusters were synthesized with control over Li:Nb ratio as precursors for LiNbO{sub 3} films. • X-ray scattering studies in solution and the solid-state revealed differences controlled by Li:Nb ratio. • Film deposition studies revealed phase, composition and morphology is controlled by Li:Nb ratio. • Cluster to film transformation was revealed using total X-ray scattering and TGA.

  7. Cation-Exchange Equilibria with Fused Salts

    International Nuclear Information System (INIS)

    Solute distributions of alkali metal, alkaline- earth, transition metal, and actinide ions have been studied in fused salt-cation exchanger systems. The fused salts employed were alkali halides and nitrates. The cation exchangers used were natural zeolites, synthetic zeolites, high-porosity glasses, and molten oxide mixtures. The molten exchangers were composed of Na2O and B2O3 in various proportions. The relative quantities not only determined the exchanger capacity and electrolyte penetration but also produced distribution coefficients for a given solute which varied over several orders of magnitude. Moreover, they produced marked reversals in the selectivity series. Additional studies on the anion distributions, miscibility diagrams, vapour pressures and diffusion rates in these systems have elucidated the mechanisms involved and the relation of selectivity to solute properties, system thermodynamics, exchanger structure and available functional groups. In the region of high Na2O composition, the distribution coefficients for mono-, di- and trivalent cations in NaCl have not only the same order of selectivity found in Dowex 50-HCl systems but also similar values for the distribution coefficients. The results are summarized qualitatively and compared to behaviour in aqueous systems (Table VII). (author)

  8. The Application of Corporate Identity System (CIS) in Chinese Salt Industry Companies and Salt Brands%论CIS在我国食盐企业和品牌中的应用

    Institute of Scientific and Technical Information of China (English)

    赵月华

    2012-01-01

    Corporate Identity System is a systematic engineering method, which aims at promoting corporation's image building in an all-round and orderly way. The introduction of this system has become a long - term competitive strategy of Chinese salt especially table salt industry companies. The establishment of Corporate Identity System on salt industry companies could be realized in the principle of a clear - specified inner parts, framework as well as function, by such important measures as optimizing brands' image design, respecting public relations and advertisement, improving quality and service, and implementing the overall planning and development.%企业形象识别系统(CorporateIdentitySystem),是企业由内而外有计划地展现形象的系统工程.引进这一系统,已成为我国盐业企业特别是食盐企业的一项长期竞争战略.建立食盐企业形象识别系统,要在明确该系统的内涵、构架和功能的基础上,采取优化品牌整体形象设计、重视公关与广告、提高内在质量与服务水平、实施统筹规划建设等重要措施.

  9. Effects of organic acids, amino acids and ethanol on the radio-degradation of patulin in an aqueous model system

    International Nuclear Information System (INIS)

    The effects of organic acids, amino acids, and ethanol on the radio-degradation of patulin by gamma irradiation in an aqueous model system were investigated. The patulin, dissolved in distilled water at a concentration of 50 ppm, was practically degraded by the gamma irradiation at the dose of 1.0 kGy, while 33% of the patulin remained in apple juice. In the aqueous model system, the radio-degradation of patulin was partially inhibited by the addition of organic acids, amino acids, and ethanol. The proportions of remaining patulin after irradiation with the dose of 1.0 kGy in the 1% solution of malic acid, citric acid, lactic acid, acetic acid, ascorbic acid, and ethanol were 31.4%, 2.3%, 31.2%, 6.1%, 50.8%, and 12.5%, respectively. During 30 days of storage, the remaining patulin was reduced gradually in the solution of ascorbic acid and malic acid compared to being stable in other samples. The amino acids, serine, threonine, and histidine, inhibited the radio-degradation of patulin. In conclusion, it was suggested that 1 kGy of gamma irradiation (recommended radiation doses for radicidation and/or quarantine in fruits) is effective for the reduction of patulin, but the nutritional elements should be considered because the radio-degradation effects are environment dependent

  10. Mixed system of ionic liquid and non-ionic surfactants in aqueous media: Surface and thermodynamic properties

    International Nuclear Information System (INIS)

    Highlights: • Interaction of ionic liquid and ethylene oxide based non-ionic surfactants in aqueous media. • Evaluation of various surface properties and thermodynamic parameters. • Micellar growth ensues from exothermic to endothermic with increase in temperature. • Micelle formation is enthalpy driven at low temperature and entropy driven at higher temperature. • The micellization power and adsorption proficiency decreased at high IL concentrations. - Abstract: The mixed system of ionic liquid (IL) tetraethyl ammonium tetrafluoroborate [TEA(BF4)] and numerous ethylene oxide based non-ionic surfactants in aqueous media were studied using surface tension, viscosity and dynamic light scattering (DLS) measurements. Various surface properties like critical micelle concentration (cmc), maximum surface excess concentration (Γmax), minimum surface area per surfactant molecule (Amin), surface tension at the cmc (γcmc), adsorption efficiency (pC20), and effectiveness of surface tension reduction (πcmc) as well as thermodynamic parameters of micellization have been determined. DLS and viscosity measurements revealed that the micellar growth was attributed to the bridged solvophilicity of the POE chain in surfactants at elevated temperatures. In most of the cases, the progression ensues from exothermic to endothermic with increase in temperature of the mixed system. Thermodynamic parameter indicates that the micelle formation process is enthalpy driven at low temperature and entropy driven at higher temperature

  11. Effects of organic acids, amino acids and ethanol on the radio-degradation of patulin in an aqueous model system

    Energy Technology Data Exchange (ETDEWEB)

    Yun, Hyejeong [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, Chonbuk, Jeongeup 580-185 (Korea, Republic of); Department of Food Science and Technology, Kyungpook National University, Daegu 702-701 (Korea, Republic of); Lim, Sangyong [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, Chonbuk, Jeongeup 580-185 (Korea, Republic of); Jo, Cheorun [Department of Animal Science and Biotechnology, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Chung, Jinwoo [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, Chonbuk, Jeongeup 580-185 (Korea, Republic of); Kim, Soohyun [Glycomics Team, Korea Basic Science Institute, Daejeon 305-333 (Korea, Republic of); Kwon, Joong-Ho [Department of Food Science and Technology, Kyungpook National University, Daegu 702-701 (Korea, Republic of); Kim, Dongho [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, Chonbuk, Jeongeup 580-185 (Korea, Republic of)], E-mail: fungikim@kaeri.re.kr

    2008-06-15

    The effects of organic acids, amino acids, and ethanol on the radio-degradation of patulin by gamma irradiation in an aqueous model system were investigated. The patulin, dissolved in distilled water at a concentration of 50 ppm, was practically degraded by the gamma irradiation at the dose of 1.0 kGy, while 33% of the patulin remained in apple juice. In the aqueous model system, the radio-degradation of patulin was partially inhibited by the addition of organic acids, amino acids, and ethanol. The proportions of remaining patulin after irradiation with the dose of 1.0 kGy in the 1% solution of malic acid, citric acid, lactic acid, acetic acid, ascorbic acid, and ethanol were 31.4%, 2.3%, 31.2%, 6.1%, 50.8%, and 12.5%, respectively. During 30 days of storage, the remaining patulin was reduced gradually in the solution of ascorbic acid and malic acid compared to being stable in other samples. The amino acids, serine, threonine, and histidine, inhibited the radio-degradation of patulin. In conclusion, it was suggested that 1 kGy of gamma irradiation (recommended radiation doses for radicidation and/or quarantine in fruits) is effective for the reduction of patulin, but the nutritional elements should be considered because the radio-degradation effects are environment dependent.

  12. Chelate-Modified Fenton Reaction for the Degradation of Trichloroethylene in Aqueous and Two-Phase Systems

    Energy Technology Data Exchange (ETDEWEB)

    Lewis, Scott [Univ of KY, dept of chemical and materials engineering; lynch, Andrew [Univ of KY, dept of chemical and materials engineering; Bachas, Leonidas [Univ of KY, Dept of Chemistry; hampson, Steve [Univ of KY Center for Applied Energy Research - KY Research Consortium of Energy and Environment; Ormsbee, Lindelle [Univ of KY Center for Applied Energy Research - KY Research Consortium of Energy and Environment; Bhattacharyya, Dibakar [Univ of KY, dept of chemical and materials engineering

    2008-06-01

    The Standard Fenton reaction has been used for In-Situ Chemical Oxidation (ISCO) of toxic organics in groundwater. However, it requires low pH operating conditions, and thus has limitations for in situ applications. In addition, hydroxyl radicals are rapidly consumed by hydroxyl scavengers found in the subsurface. These problems are alleviated through the chelate-modified Fenton (hydroxyl radical) reaction, which includes the addition of nontoxic chelate (L) such as citrate or gluconic acid. This chelate allows the reaction to take place at bear neutral pH and control hydrogen peroxide consumption by binding to Fe(II), forming an FeL complex. The chelate also binds to Fe(III), preventing its precipitation as ferric hydroxide and thus prevents problems associated with injection well plugging. The rate of TCE dechlorination in chelate-modified Fenton systems is a function of pH, H2O2 concentration, and FE:L ratio. The primary objective of this research is to model and apply this process to the destruction of trichloroethylene (TCE) present in both the aqueous and organic (in the form of droplets) phases. Experimentation proved the chelate-modified Fenton reaction effectively dechlorinates TCE in both the aqueous and organic phases at near-neutral pH. Other focuses of this work include determining the effect of [L]:[Fe] ratios on H2O2 and TCE degradation as well as reusability of the FE citrate solution under repeated H2O2 injections. Generalized models were developed to predict the concentration of TCE in the aqueous phase and TCE droplet radius as a function of time using established hydroxyl radial kinetics and mass transfer relationships.

  13. Perchlorate production by ozone oxidation of chloride in aqueous and dry systems

    International Nuclear Information System (INIS)

    Overwhelming evidence now exists that perchlorate is produced through natural processes and can be ubiquitously found at environmentally relevant concentrations in arid and semi-arid locations. A number of potential production mechanisms have been hypothesized and ClO4- production by ozone oxidation of surface bound Cl- was demonstrated. However, no information concerning the impact of concentration, final reaction products distribution, impact of reaction phase, or oxidation of important oxychlorine intermediates has been reported. Using IC-MS-MS analysis and replicate oxidation experiments, we show that exposing aqueous solutions or Cl- coated sand or glass surfaces to O3 (0.96%) generated ClO4- with molar yields of 0.007 and 0.01% for aqueous Cl- solutions and 0.025 and 0.42% for Cl- coated sand and glass, respectively. Aqueous solutions of Cl- produced less ClO4- than Cl- coated sand or glass as well as a higher ratio of ClO3- to ClO4-. Reduction of the initial Cl- mass resulted in substantially higher molar yields of ClO4- and ClO3-. In addition, alkaline absorbers that captured gaseous products contained substantial quantities of Cl-, ClO3-, and ClO4-. Solutions of possible oxychlorine intermediates (OCl- and ClO3-) exposed to O3 produced only scant amounts of ClO4- while a ClO2- solution exposed to O3 produced substantial molar yields of ClO4- (4% molar yield). Scanning electron microscopy coupled with energy energy-dispersive X-ray analysis demonstrated a significant loss of Cl- and an increase in oxygen on the Cl- coated silica sand exposed to O3. While the experimental conditions are not reflective of natural conditions this work clearly demonstrates the relative potential of Cl- precursors in perchlorate production and the likely importance of dry aerosol oxidation over solution phase reactions. It also suggests that ClO2- may be a key intermediate while ClO3- and OCl- are unlikely to play a significant role

  14. Kinetics of Methane Hydrate Formation in Pure Water and Inhibitor Containing Systems

    Institute of Scientific and Technical Information of China (English)

    QIUJunhong; GUOTianmin

    2002-01-01

    Kinetic data of methane hydrate formation in the presence of pure water,brines with single salt and mixed salts,and aqueous solutions of ethylene glycol(EG) and salt+EG were measured.A new kinetic model of hydrate formation for the methane+water systems was developed based on a four-step formation mechanism and reaction kinetic approach.The proposed kinetic model predicts the kinetic behavior of methane hydrate formation in pure water with good accuracy.The feasibility of extending the kenetic model of salt(s) and EG containing systems was explored.

  15. Liquid-liquid distribution of B group vitamins in polyethylene glycol-based systems

    Science.gov (United States)

    Korenman, Ya. I.; Zykov, A. V.; Mokshina, N. Ya.

    2011-05-01

    General regularities of the liquid-liquid distribution of B1, B2, B6, and B12 vitamins in aqueous polyethylene glycol (PEG-2000, PEG-5000) solution-aqueous salt solution systems are studied. The influence of the salting-out agent, the concentration of the polymer, and its molecular weight on the distribution coefficients and recovery factors of the vitamins are considered. Equations relating the distribution coefficients (log D) to the polymer concentration are derived.

  16. FY'99 final report for the expedited technology demonstration project: demonstration test results for the MSO/off-gas and salt recycle system

    International Nuclear Information System (INIS)

    Molten Salt Oxidation (MSO) is a promising alternative to incineration for the treatment of a variety of organic wastes. Lawrence Livermore National Laboratory (LLNL) has prepared a facility in which an integrated pilot-scale MSO treatment system is being tested and demonstrated. The system consists of a MSO vessel with a dedicated off-gas treatment system, a salt recycle system, feed preparation equipment, and a ceramic final waste forms immobilization system. This integrated system was designed and engineered based on operational experience with an engineering-scale reactor unit and extensive laboratory development on salt recycle and final forms preparation. The MSO/off-gas system has been operational since December 1997. The salt recycle system and the ceramic final forms immobilization became operational in May 1998. In FY98, we have tested the MSO facility with various organic feeds, including chlorinated solvents, tributyl phosphate/kerosene, PCB-contaminated waste oils and solvents, booties, plastic pellets, ion exchange resins, activated carbon, radioactive-spiked organics, and well-characterized low-level liquid mixed wastes. MSO is shown to be a versatile technology for hazardous waste treatment and may be a solution to many waste disposal problems in DOE sites. The results of the demonstration conducted in FY98 has been reported [1]. In FY99 (October 1998 to April 1999) we conducted further testing in the MSO/off-gas system with ion exchange resins, two real waste specimens, activated carbon, and TNT-loaded activated carbon, both at regular feed rates and higher feed rates up to a superficial gas velocity of 1.75 ft/s. We also drained the salt three times (SR7, SR8, SR9) in FY99 and sent the spent salts to the salt recycle system for further processing. This report presents the results obtained from the demonstration of the MSO/off-gas system and the salt recycle system from October 1998 to April 1999. We then shut down the operation and cleaned the

  17. Photodegradation of 2,4-Dichlorophenol in Aqueous Systems under Simulated and Natural Sunlight

    Directory of Open Access Journals (Sweden)

    Dorota Gryglik

    2016-01-01

    Full Text Available The work presents results of studies on 2,4-dichlorophenol (2,4-DCP degradation in aqueous solutions using photochemically initiated processes by simulated and natural sunlight. A number of possible substrate photodegradation routes were investigated, by both direct photolysis and photosensitized oxidation process. The major role of singlet oxygen in 2,4-DCP photodegradation was proved. Rose Bengal and derivatives of porphine and phthalocyanine were used as sensitizers. The influences of various process parameters on the reaction rate were investigated. On the basis of experimental data reaction rate constants of 2,4-DCP photosensitized oxidation were determined. The possibility of using natural sunlight to degrade 2,4-DCP in water in the middle latitudes was stated. The acute toxicity bioassay was conducted with the marine bacterium Vibrio fischeri as a bioluminescent indicator. The obtained results encourage further research on this process.

  18. Evolution of hydrologic systems and brine geochemistry in a deforming salt medium: Data from WIPP brine seeps

    Energy Technology Data Exchange (ETDEWEB)

    Deal, D.E. (I. T. Corp., Carlsbad, NM (USA)); Roggenthen, W.M. (South Dakota School of Mines and Technology, Rapid City, SD (USA). Dept. of Geology and Geological Engineering)

    1991-01-01

    The Brine Sampling and Evaluation Program (BSEP) is a formalized continuation of studies that began in 1982 as part of the Site Validation Program. The program was established in 1985. The mission was to document and investigate the origins, hydraulic characteristics, extent, and composition of brine occurrences in the Permian Salado Formation and the seepage of that brine into the WIPP excavations. This document focuses on the cumulative data obtained from the BSEP. The overall activities of the BSEP described and quantified the brine. It includes documentation and study of brine inflow into boreholes in the facility. The BSEP investigated the occurrence and development of brine weeps, crusts, and brine geochemistry. The presence of salt-tolerant bacteria in the workings was recorded and their possible interactions with experiments and operations, was assessed. The formation properties associated with the occurrence of brine was characterized. The determination of formation properties included the water content of various geologic units, direct examination of these units in boreholes using a video camera system, and measurement of electrical properties relatable to the brine contents. Modeling examined the interaction of salt deformation near the workings and the flow of brine through the deforming rocks. 34 refs.

  19. Evolution of hydrologic systems and brine geochemistry in a deforming salt medium: Data from WIPP brine seeps

    International Nuclear Information System (INIS)

    The Brine Sampling and Evaluation Program (BSEP) is a formalized continuation of studies that began in 1982 as part of the Site Validation Program. The program was established in 1985. The mission was to document and investigate the origins, hydraulic characteristics, extent, and composition of brine occurrences in the Permian Salado Formation and the seepage of that brine into the WIPP excavations. This document focuses on the cumulative data obtained from the BSEP. The overall activities of the BSEP described and quantified the brine. It includes documentation and study of brine inflow into boreholes in the facility. The BSEP investigated the occurrence and development of brine weeps, crusts, and brine geochemistry. The presence of salt-tolerant bacteria in the workings was recorded and their possible interactions with experiments and operations, was assessed. The formation properties associated with the occurrence of brine was characterized. The determination of formation properties included the water content of various geologic units, direct examination of these units in boreholes using a video camera system, and measurement of electrical properties relatable to the brine contents. Modeling examined the interaction of salt deformation near the workings and the flow of brine through the deforming rocks. 34 refs

  20. Microbial degradation of phosmet on blueberry fruit and in aqueous systems by indigenous bacterial flora on lowbush blueberries (Vaccinium angustifolium).

    Science.gov (United States)

    Crowe, K M; Bushway, A A; Bushway, R J; Davis-Dentici, K

    2007-10-01

    Phosmet-adapted bacteria isolated from lowbush blueberries (Vaccinium angustifolium) were evaluated for their ability to degrade phosmet on blueberry fruit and in minimal salt solutions. Microbial metabolism of phosmet by isolates of Enterobacter agglomerans and Pseudomonas fluorescens resulted in significant reductions (P agglomerans or P. fluorescens and supplemented with phosmet or phosmet and glucose. Microbial degradation concurrent with the proliferation of P. fluorescens was similar in both liquid systems, indicative of preferential utilization of phosmet as an energy substrate. E. agglomerans exhibited the ability to degrade phosmet as a carbon source, yet in the presence of added glucose, phosmet degradation occurred within the 1st 24 h only followed by total population mortality resulting in no appreciable degradation. Characteristic utilization of glucose by this isolate suggests a possible switch in carbon substrate utilization away from phosmet, which resulted in toxicity from the remaining phosmet. Overall, microbial metabolism of phosmet as an energy source resulted in significant degradation of residues on blueberries and in minimal salt solutions. Thus, the role of adapted strains of E. agglomerans and P. fluorescens in degrading phosmet on blueberries represents an extensive plant-microorganism relationship, which is essential to determination of phosmet persistence under pre- and postharvest conditions. PMID:17995608