WorldWideScience

Sample records for aqueous phase source

  1. Motile Geobacter dechlorinators migrate into a model source zone of trichloroethene dense non-aqueous phase liquid: Experimental evaluation and modeling

    Science.gov (United States)

    Philips, Jo; Miroshnikov, Alexey; Haest, Pieter Jan; Springael, Dirk; Smolders, Erik

    2014-12-01

    Microbial migration towards a trichloroethene (TCE) dense non-aqueous phase liquid (DNAPL) could facilitate the bioaugmentation of TCE DNAPL source zones. This study characterized the motility of the Geobacter dechlorinators in a TCE to cis-dichloroethene dechlorinating KB-1™ subculture. No chemotaxis towards or away from TCE was found using an agarose in-plug bridge method. A second experiment placed an inoculated aqueous layer on top of a sterile sand layer and showed that Geobacter migrated several centimeters in the sand layer in just 7 days. A random motility coefficient for Geobacter in water of 0.24 ± 0.02 cm2·day- 1 was fitted. A third experiment used a diffusion-cell setup with a 5.5 cm central sand layer separating a DNAPL from an aqueous top layer as a model source zone to examine the effect of random motility on TCE DNAPL dissolution. With top layer inoculation, Geobacter quickly colonized the sand layer, thereby enhancing the initial TCE DNAPL dissolution flux. After 19 days, the DNAPL dissolution enhancement was only 24% lower than with an homogenous inoculation of the sand layer. A diffusion-motility model was developed to describe dechlorination and migration in the diffusion-cells. This model suggested that the fast colonization of the sand layer by Geobacter was due to the combination of random motility and growth on TCE.

  2. The role of a detailed aqueous phase source release model in the LANL area G performance assessment

    Energy Technology Data Exchange (ETDEWEB)

    Vold, E.L.; Shuman, R.; Hollis, D.K. [Los Alamos National Lab., NM (United States)] [and others

    1995-12-31

    A preliminary draft of the Performance Assessment for the Los Alamos National Laboratory (LANL) low-level radioactive waste disposal facility at Area G is currently being completed as required by Department of Energy orders. A detailed review of the inventory data base records and the existing models for source release led to the development of a new modeling capability to describe the liquid phase transport from the waste package volumes. Nuclide quantities are sorted down to four waste package release categories for modeling: rapid release, soil, concrete/sludge, and corrosion. Geochemistry for the waste packages was evaluated in terms of the equilibrium coefficients, Kds, and elemental solubility limits, Csl, interpolated from the literature. Percolation calculations for the base case closure cover show a highly skewed distribution with an average of 4 mm/yr percolation from the disposal unit bottom. The waste release model is based on a compartment representation of the package efflux, and depends on package size, percolation rate or Darcy flux, retardation coefficient, and moisture content.

  3. Oxidation of Glyoxal in the Aqueous Phase

    Science.gov (United States)

    Schaefer, Thomas; Herrmann, Hartmut

    2014-05-01

    Large amounts of volatile organic compounds (VOCs) are emitted into the atmosphere from biogenic and anthropogenic sources. The emitted VOCs can be further oxidized in the gas phase as well as in the aqueous phase (cloud droplets, fog, rain and deliquescent particles) to form semivolatile carbonyl compounds. For example, the carbonyl compound glyoxal can be produced by the oxidation process of isoprene. Additionally, these semivolatile carbonyl compounds might be important for the formation of secondary organic aerosol (SOA) by partitioning between gas- and liquid phase of pre-existing particles. In the gas phase as well as in the aqueous phase (cloud droplets, fog, rain and deliquescent particles) these compounds can be further oxidized, e.g., by radicals (OH and NO3) leading to peroxy radicals and then to substituted organics. Two concepts exist in the literature to describe the glyoxal oxidation pathway via alkyl radicals to the peroxy radicals by the addition of molecular oxygen. The first one[1] states that peroxy radical formation occurs with a rate constant of k = 1 × 109 M-1 s-1. The second concept[2] assumes that this is a minor reaction pathway because of the lower rate constant of k = 1 × 106 M-1 s-1. The difference in the rate constants of the oxygen addition is of about three orders of magnitude which might lead to different oxidation products and yields in aqueous solution. In the present work, the formation and the decay of the formed glyoxyl radicals and glyoxyl peroxy radicals were studied in low and high concentrated oxygen solutions using a laser photolysis long path absorption setup (LP-LPA). To clarify the difference a method introduced by Adams et al., 1969[3] to measure the rate constant of the oxygen addition on alkyl radical was modified for laser flash photolysis conditions and successfully applied. In this study a rate constant for the addition reaction of molecular oxygen of k = 8 × 108 M-1 s-1 was measured. This clearly indicates

  4. Source Wavelet Phase Extraction

    Science.gov (United States)

    Naghadeh, Diako Hariri; Morley, Christopher Keith

    2016-06-01

    Extraction of propagation wavelet phase from seismic data can be conducted using first, second, third and fourth-order statistics. Three new methods are introduced, which are: (1) Combination of different moments, (2) Windowed continuous wavelet transform and (3) Maximum correlation with cosine function. To compare different methods synthetic data with and without noise were chosen. Results show that first, second and third order statistics are not able to preserve wavelet phase. Kurtosis can preserve propagation wavelet phase but signal-to-noise ratio can affect the extracted phase using this method. So for data set with low signal-to-noise ratio, it will be unstable. Using a combination of different moments to extract the phase is more robust than applying kurtosis. The improvement occurs because zero phase wavelets with reverse polarities have equal maximum kurtosis values hence the correct wavelet polarity cannot be identified. Zero-phase wavelets with reverse polarities have minimum and maximum values for a combination of different-moments method. These properties enable the technique to handle a finite data segment and to choose the correct wavelet polarity. Also, the existence of different moments can decrease sensitivity to outliers. A windowed continuous wavelet transform is more sensitive to signal-to-noise ratio than the combination of different-moments method, also if the scale for the wavelet is incorrect it will encounter with more problems to extract phase. When the effects of frequency bandwidth, signal-to-noise ratio and analyzing window length are considered, the results of extracting phase information from data without and with noise demonstrate that combination of different-moments is superior to the other methods introduced here.

  5. Advanced Aqueous Phase Catalyst Development using Combinatorial Methods Project

    Data.gov (United States)

    National Aeronautics and Space Administration — The use of combinatorial methods is proposed to rapidly screen catalyst formulations for the advanced development of aqueous phase oxidation catalysts with greater...

  6. Segregative phase separation in aqueous mixtures of polydisperse biopolymers

    NARCIS (Netherlands)

    Edelman, M.W.

    2003-01-01

    Keywords: biopolymer, gelatine, dextran, PEO, phase separation, polydispersity, molar mass distribution, SEC-MALLS, CSLM The temperature-composition phase diagram of aqueous solutions of gelatine and dextran, which show liquid/liquid phase segregation, were explored at temperatures above the gelatio

  7. Donnan potentials in aqueous phase-separated polymer mixtures

    NARCIS (Netherlands)

    Vis, Mark; Peters, Vincent F D; Tromp, R. Hans; Erné, Ben H.

    2014-01-01

    A promising approach to texturize water is by the addition of mutually incompatible polymers, leading to phase separation. Here, we demonstrate that the phase stability of aqueous polymer solutions is affected not only by chemical differences between the polymers but also by their electric charge. D

  8. 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

  9. Charged hydrophobic colloids at an oil-aqueous phase interface

    Science.gov (United States)

    Kelleher, Colm P.; Wang, Anna; Guerrero-García, Guillermo Iván; Hollingsworth, Andrew D.; Guerra, Rodrigo E.; Krishnatreya, Bhaskar Jyoti; Grier, David G.; Manoharan, Vinothan N.; Chaikin, Paul M.

    2015-12-01

    Hydrophobic poly(methyl methacrylate) (PMMA) colloidal particles, when dispersed in oil with a relatively high dielectric constant, can become highly charged. In the presence of an interface with a conducting aqueous phase, image-charge effects lead to strong binding of colloidal particles to the interface, even though the particles are wetted very little by the aqueous phase. We study both the behavior of individual colloidal particles as they approach the interface and the interactions between particles that are already interfacially bound. We demonstrate that using particles which are minimally wetted by the aqueous phase allows us to isolate and study those interactions which are due solely to charging of the particle surface in oil. Finally, we show that these interactions can be understood by a simple image-charge model in which the particle charge q is the sole fitting parameter.

  10. Characterization of complex non-aqueous phase liquids (NAPLs) in the subsurface environment: partitioning and interfacial tracer tests and numerical dissolution assessment

    OpenAIRE

    Piepenbrink, Matthias

    2007-01-01

    Contamination of the subsurface environment by complex organic non-aqueous phase liquids (NAPLs) and the resulting release of carcinogenic or mutagenic organic compounds impose a serious risk on groundwater quality. Due to the low aqueous solubilities of the individual organic components the rate of mass transfer from the non-aqueous phase to the water phase is very slow, thus NAPL source zones typically represent long-term contamination problems with organic compounds leaching into the...

  11. Modeling Non-aqueous Phase Liquid Displacement Process

    Institute of Scientific and Technical Information of China (English)

    Yang Zhenqing; Shao Changjin; Zhou Guanggang; Qiu Chao

    2007-01-01

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

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

    Science.gov (United States)

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

    2016-07-21

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

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

    OpenAIRE

    Kneafsey, Timothy J.; HUNT, JAMES R.

    2004-01-01

    Many non-aqueous phase liquids (NAPLs) are expected to spread at the air – water interface, particularly under non-equilibrium conditions. In the vadose zone, this spreading should increase the surface area for mass transfer and the efficiency of volatile NAPL recovery by soil vapor extraction (SVE). Observations of spreading on water wet surfaces led to a conceptual model of oil spreading vertically above a NAPL pool in the vadose zone. Analysis of this model predicts that spreading can enha...

  14. Simultaneous Separation of Manganese, Cobalt, and Nickel by the Organic-Aqueous-Aqueous Three-Phase Solvent Extraction

    Science.gov (United States)

    Shirayama, Sakae; Uda, Tetsuya

    2016-04-01

    This research outlines an organic-aqueous-aqueous three-phase solvent extraction method and proposes its use in a new metal separation process for the recycling of manganese (Mn), cobalt (Co), and nickel (Ni) from used lithium ion batteries (LIBs). The three-phase system was formed by mixing xylene organic solution, 50 pct polyethylene glycol (PEG) aqueous solution, and 1 mol L-1 sodium sulfate (Na2SO4) aqueous solution. The xylene organic solution contained 2-ethylhexylphosphonic acid (D2EHPA) as an extractant for Mn ion, and the Na2SO4 aqueous solution contained 1 mol L-1 potassium thiocyanate (KSCN) as an extractant for Co ion. Concentrations of the metal ions were varied by dissolving metal sulfates in the Na2SO4 aqueous solution. As a result of the experiments, Mn, Co, and Ni ions were distributed in the xylene organic phase, PEG-rich aqueous phase, and Na2SO4-rich aqueous phase, respectively. The separation was effective when the pH value was around 4. Numerical simulation was also conducted in order to predict the distribution of metal ions after the multi-stage counter-current extractions.

  15. Isotropic-nematic phase transition in aqueous sepiolite suspensions.

    Science.gov (United States)

    Woolston, Phillip; van Duijneveldt, Jeroen S

    2015-01-01

    Aqueous suspensions of sepiolite clay rods in water tend to form gels on increase of concentration. Here it is shown how addition of a small amount (0.1% of the clay mass) of a common stabiliser for clay suspensions, sodium polyacrylate, can allow the observation of an isotropic-nematic liquid crystal phase transition. This transition was found to move to higher clay concentrations upon adding NaCl, with samples containing 10(-3) M salt or above only displaying a gel phase. Even samples that initially formed liquid crystals had a tendency to form gels after several weeks, possibly due to Mg(2+) ions leaching from the clay mineral. PMID:25313468

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

    Science.gov (United States)

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

    2001-05-01

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

  17. Determination of protein loss during aqueous and phase partition fixation using formalin and glutaraldehyde

    Energy Technology Data Exchange (ETDEWEB)

    Mays, E.T.; Feldhoff, R.C.; Nettleton, G.S.

    1984-10-01

    In phase partition fixation tissue is immersed in an organic solvent at equilibrium with an aqueous phase containing a fixing agent. By using radioisotope labeling techniques the effects of phase partition fixation on protein retention during fixation of tissue with formalin and glutaraldehyde have been determined and compared with those of standard aqueous fixation using these fixatives. It has been shown that retention of protein in tissue during phase partition fixation was as good or better than during aqueous fixation. Improved retention provides further evidence that phase partition fixation may be a useful alternative to aqueous fixation.

  18. Bioligand-mediated partitioning of radionuclides to the aqueous phase

    International Nuclear Information System (INIS)

    The aqueous-phase partitioning of 59Fe, 147Pm, 234Th and 241Am by complexing compounds from subsurface bacteria has previously been studied in the presence of quartz sand. In this study the aqueous-phase partitioning of pico- to submicromolar amounts of 59Fe, 147Pm, 234Th and 241Am was analyzed in the presence of TiO2 and exudates from three species of subsurface bacteria: Pseudomonas fluorescens, Pseudomonas stutzeri, and Shewanella putrefaciens. All were grown under aerobic conditions and P. stutzeri and S. putrefaciens were grown under anaerobic conditions as well. The supernatants of the aerobic and anaerobic cultures were collected and radionuclide was added. TiO2, with BET surface area of 49.9 m2 x g-1, was added to the supernatant radionuclide mix, and the pH was adjusted to approximately 8. After incubation, the amount of radionuclide in the liquid phase of the samples and controls was analyzed using scintillation method. Two types of values were calculated: solution% = the activity maintained in solution relative to the total activity, and Q-values = the quotient between the activity in samples and the activity in controls. Aerobic supernatants had solution% values between 89% and 100% for 59Fe and between 18 and 43% for 234Th. The solution% values for 241Am and 147Pm were less than 2% overall, but the Q-values were between 34 and 115 times more 241Am in bacterial supernatants than in controls. The corresponding values for 147Pm ranged from 6 to 20 times more than in the control. The solution% values for all elements in the presence of anaerobic supernatants were below 2%, but the Q-values clustered around 7 for 59Fe and ranging from 2 to 29 for 234Th, indicated that anaerobic supernatants partitioned these elements to the aqueous phase. Both aerobic and anaerobic supernatants tested positive for complexing compounds when analyzed, using the Chrome Azurol S assay. Complexation with excreted organic ligands is most likely the reason for the higher amounts

  19. Representing effects of aqueous phase reactions in shallow cumuli in global models

    Science.gov (United States)

    Nie, Ji; Kuang, Zhiming; Jacob, Daniel J.; Guo, Jiahua

    2016-05-01

    Aqueous phase reactions are important, sometimes dominant (e.g., for SO2), pathways for the oxidation of air pollutants at the local and/or global scale. In many current chemical transport models (CTMs), the transport and aqueous reactions of chemical species are treated as split processes, and the subgrid-scale heterogeneity between cloudy and environmental air is not considered. Here using large eddy simulation (LES) with idealized aqueous reactions mimicking the oxidation of surface-originated SO2 by H2O2 in shallow cumuli, we show that the eddy diffusivity mass flux (EDMF) approach with a bulk plume can represent those processes quite well when entrainment/detrainment rates and eddy diffusivity are diagnosed using a conservative thermodynamic variable such as total water content. The reason is that a typical aqueous reaction such as SO2 aqueous oxidation is relatively slow compared to the in-cloud residence time of air parcels in shallow cumuli. As a result, the surface-originated SO2 is well correlated with and behaves like conservative thermodynamic variables that also have sources at the surface. Experiments with various reaction rate constants and relative abundances of SO2 and H2O2 indicate that when the reaction timescale approaches the in-cloud residence time of air parcels, the errors of the bulk plume approach start to increase. Treating chemical tracer transport and aqueous reaction as split processes leads to significant errors, especially when the reaction is fast compared to the in-cloud residence time. Overall, the EDMF approach shows large improvement over the CTM-like treatments in matching the LES results.

  20. Uranium recovery from low-level aqueous sources

    International Nuclear Information System (INIS)

    The aqueous sources of soluble uranium were surveyed and evaluated in terms of the uranium geochemical cycle in an effort to identify potential unexploited resources. Freshwater sources appeared to be too low in uranium content to merit consideration, while seawater, although very dilute (approx. 3.3 ppB), contains approx. 4 x 109 metric tons of uranium in all the world's oceans. A literature review of recent publications and patents concerning uranium recovery from seawater was conducted. Considerable experimental work is currently under way in Japan; less is being done in the European countries. An assessment of the current state of technology is presented in this report. Repeated screening programs have identified hydrous titanium oxide as the most promising candidate absorbent. However, some of its properties such as distribution coefficient, selectivity, loading, and possibly stability appear to render its use inadequate in a practical recovery system. Also, various assessments of the energy efficiency of pumped or tidal power schemes for contacting the sorbent and seawater are in major disagreement. Needed future research and development tasks are discussed. A fundamental sorbent development program to greatly improve sorbent properties would be required to permit practical recovery of uranium from seawater. Major unresolved engineering aspects of such recovery systems are also identified and discussed

  1. Polyethylene Glycol as Support and Phase Transfer Catalyst in Aqueous Palladium-catalyzed Liquid-phase Synthesis

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Excellent yields and purity were obtained in the aqueous medium Suzuki, Sonogashira, Stille and Heck reactions using palladium (Ⅱ) as catalyst in liquid phase synthesis. Polyethylene glycol (PEG) acted as soluble polymeric support and phase transfer catalyst as well.

  2. Structure and phase behavior of aqueous methylcellulose solutions

    Science.gov (United States)

    McAllister, John; Schmidt, Peter; Lodge, Timothy; Bates, Frank

    2015-03-01

    Cellulose ethers (CE) constitute a multi-billion dollar industry, and have found end uses in a broad array of applications from construction materials, food products, personal care products, and pharmaceuticals for more than 80 years. Methylcellulose (MC, with the trade name METHOCEL™) is a CE in which there is a partial substitution of -OH groups with -OCH3 groups. This results in a polymer that is water-soluble at low temperatures, and aqueous solutions of MC display gelation and phase separation at higher temperatures. The nature of MC gelation has been debated for many years, and this project has made significant advances in the understanding of the solution properties of CEs. We have characterized a fibrillar structure of MC gels by cryogenic transmission electron microscopy (cryo-TEM) and small angle neutron scattering (SANS). Using light scattering, turbidity measurements, and dynamic mechanical spectroscopy (DMS) we report that MC microphase separates by nucleation and growth of fibril aggregates, and is a different process from LCST phase separation.

  3. Aqueous-phase behavior of natural glycolipid biosurfactant mannosylerythritol lipid A: sponge, cubic, and lamellar phases.

    Science.gov (United States)

    Imura, Tomohiro; Hikosaka, Yusuke; Worakitkanchanakul, Wannasiri; Sakai, Hideki; Abe, Masahiko; Konishi, Masaaki; Minamikawa, Hiroyuki; Kitamoto, Dai

    2007-02-13

    The aqueous-phase behavior of mannosylerythritol lipid A (MEL-A), which is a glycolipid biosurfactant produced from vegetable oils by yeast strains of the genus Pseudozyma, was investigated using polarized optical microscopy, small-angle X-ray scattering (SAXS), and differential scanning calorimetry (DSC). MEL-A was found to self-assemble into a variety of distinctive lyotropic liquid crystals including sponge (L3), bicontinuous cubic (V2), and lamella (Lalpha) phases. On the basis of SAXS measurements, we determined the structure of the liquid crystals. The estimated lattice constant for Lalpha was 3.58 nm. DSC measurement revealed that the phase transition enthalpies from the liquid crystal to the fluid isotropic phase were in the range of 0.22-0.44 kJ/mol. Although the present MEL-A phase diagram closely resembled that obtained from relatively hydrophobic poly(oxyethylene) or fluorinated surfactants, the MEL-A L3 region was spread considerably over a wide temperature range (20-65 degrees C) compared to L3 of those surfactants: this is probably due to the unique structure which is molecularly engineered by microorganisms. In this paper, we clarify the aqueous phase diagram of the natural glycolipid biosurfactant MEL-A, and we suggest that the obtained lyotropic crystals are potentially useful as novel nanostructured biomaterials. PMID:17279642

  4. Propene Hydroformylation by Supported Aqueous-phase Rh-NORBOS Catalysts

    DEFF Research Database (Denmark)

    Riisager, Anders; Eriksen, Kim Michael; Hjortkjær, Jes;

    2003-01-01

    The gas-phase hydroformylation reaction of propene using supported aqueous-phase (SAP) Rh-NORBOS modified catalysts in a continuous flow reactor has been examined. SAP catalysts supported on six different support materials were made by wet impregnation using solutions of the precursor complex Rh(....... Based on these results the aqueous and the homogeneous nature of the SAP catalysts are discussed....

  5. Advanced Aqueous Phase Catalyst Development using Combinatorial Methods Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Combinatorial methods are proposed to develop advanced Aqueous Oxidation Catalysts (AOCs) with the capability to mineralize organic contaminants present in...

  6. A directly phase-modulated light source

    CERN Document Server

    Yuan, Z L; Lucamarini, M; Roberts, G L; Dynes, J F; Shields, A J

    2016-01-01

    The art of imparting information onto a light wave by optical signal modulation is fundamental to all forms of optical communication. Among many schemes, direct modulation of laser diodes stands out as a simple, robust, and cost effective method. However, the simultaneous changes in intensity, frequency and phase are a drawback which has prevented its application in the field of secure quantum communication. Here, we propose and experimentally demonstrate a directly phase-modulated light source which overcomes the main disadvantages associated with direct modulation and is suitable for diverse applications such as coherent communications and quantum cryptography. The source separates the tasks of phase preparation and pulse generation between a pair of semiconductor lasers leading to very pure phase states. Moreover, the cavity enhanced electro-optic effect enables the first example of sub-volt halfwave phase modulation at high signal rates. The source is compact, stable and versatile, and we show its potenti...

  7. 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.

  8. Hydrogen production by aqueous phase reforming of light oxygenated hydrocarbons

    Science.gov (United States)

    Shabaker, John William

    Aqueous phase reforming (APR) of renewable oxygenated hydrocarbons (e.g., methanol, ethylene glycol, glycerol, sorbitol, glucose) is a promising new technology for the catalytic production of high-purity hydrogen for fuel cells and chemical processing. Supported Pt catalysts are effective catalysts for stable and rapid H2 production at temperatures near 500 K (H 2 turnover frequencies near 10 min-1). Inexpensive Raney Ni-based catalysts have been developed using a combination of fundamental and high-throughput studies that have similar catalytic properties as Pt-based materials. Promotion of Raney Ni with Sn by controlled surface reaction of organometallic tin compounds is necessary to control formation of thermodynamically-favorable alkane byproducts. Detailed characterization by Mossbauer spectroscopy, electron microscopy, adsorption studies, and x-ray photoelectron spectroscopy (XPS/ESCA) has shown that NiSn alloys are formed during heat treatment, and may be responsible for enhanced stability and selectivity for hydrogen production. Detailed kinetic studies led to the development of a kinetic mechanism for the APR reaction on Pt and NiSn catalysts, in which the oxygenate decomposes through C--H and O--H cleavage, followed by C--C cleavage and water gas shift of the CO intermediate. The rate limiting step on Pt surfaces is the initial dehydrogenation, while C--C cleavage appears rate limiting over NiSn catalysts. Tin promotion of Raney Ni catalysts suppresses C--O bond scission reactions that lead to alkane formation without inhibiting fast C--C and C--H cleavage steps that are necessary for high rates of reforming. A window of operating temperature, pressure, and reactor residence time has been identified for use of the inexpensive NiSn catalysts as a Pt substitute. Concentrated feed stocks and aggressive pretreatments have been found to counteract catalyst deactivation by sintering in the hydrothermal APR environment and allow stable, long-term production of H

  9. Bioaugmentation for treatment of dense non-aqueous phase liquid in fractured sandstone blocks.

    Science.gov (United States)

    Schaefer, Charles E; Towne, Rachael M; Vainberg, Simon; McCray, John E; Steffan, Robert J

    2010-07-01

    Laboratory experiments were performed in discretely fractured sandstone blocks to evaluate the use of bioaugmentation to treat residual dense non-aqueous phase liquid (DNAPL) tetrachloroethene (PCE). Significant dechlorination of PCE and growth of Dehalococcoides spp. (DHC) occurred within the fractures. DNAPL dissolution was enhanced during bioaugmentation by up to a factor of approximately 3.5, with dissolved PCE concentrations at or near aqueous solubility. The extent of dechlorination and DNAPL dissolution enhancement were dependent upon the fracture characteristics, residence time in the fractures, and dissolved concentration of PCE. No relationship was observed between planktonic DHC concentrations exiting the fracture and the observed extents of PCE dechlorination and DNAPL dissolution. Measured planktonic DHC concentrations exiting the fracture increased with increasing flow rate and bioaugmentation dosage, suggesting that these parameters may be important for distribution of DHC to treat dissolved chlorinated ethenes migrating downgradient of the DNAPL source. Bioaugmentation dosage, for the DHC dosages and conditions studied, did not have a measurable impact on DNAPL dissolution or dechlorination within the fractures themselves. Overall, these results indicate that bioaugmentation may be a viable remedial option for treating DNAPL sources in bedrock.

  10. Secondary organic aerosol (trans)formation through aqueous phase guaiacol photonitration: chemical characterization of the products

    Science.gov (United States)

    Grgić, Irena; Kitanovski, Zoran; Kroflič, Ana; Čusak, Alen

    2014-05-01

    One of the largest primary sources of organic aerosol in the atmosphere is biomass burning (BB) (Laskin et al. 2009); in Europe its contribution to annual mean of PM10 is between 3 and 14 % (Maenhaut et al. 2012). During the process of wood burning many different products are formed via thermal degradation of wood lignin. Hardwood burning produces mainly syringol (2,6-dimetoxyphenol) derivatives, while softwood burning exclusively guaiacol (2-methoxyphenol) and its derivatives. Taking into account physical properties of methoxyphenols only, their concentrations in atmospheric waters might be underestimated. So, their aqueous phase reactions can be an additional source of SOA, especially in regions under significant influence of wood combustion. An important class of compounds formed during physical and chemical aging of the primary BBA in the atmosphere is nitrocatechols, known as strong absorbers of UV and Vis light (Claeys et al. 2012). Very recently, methyl-nitrocatechols were proposed as suitable markers for highly oxidized secondary BBA (Iinuma et al. 2010, Kitanovski et al. 2012). In the present work, the formation of SOA through aqueous phase photooxidation and nitration of guaiacol was examined. The key objective was to chemically characterize the main low-volatility products and further to check their possible presence in the urban atmospheric aerosols. The aqueous phase reactions were performed in a thermostated reactor under simulated sunlight in the presence of H2O2 and nitrite. Guaiacol reaction products were first concentrated by solid-phase extraction (SPE) and then subjected to semi-preparative liquid chromatography.The main product compounds were fractionated and isolated as pure solids and their structure was further elucidated by using nuclear magnetic resonance spectroscopy (1H, 13C and 2D NMR) and direct infusion negative ion electro-spray ionization tandem mass spectrometry (( )ESI-MS/MS). The main photonitration products of guaiacol (4

  11. Formation of aqueous-phase α-hydroxyhydroperoxides (α-HHP): potential atmospheric impacts

    OpenAIRE

    Zhao, R.; A. K. Y. Lee; Soong, R; Simpson, A. J.; J. P. D. Abbatt

    2013-01-01

    The focus of this work is on quantifying the degree of the aqueous-phase formation of α-hydroxyhydroperoxides (α-HHPs) via reversible nucleophilic addition of H2O2 to aldehydes. Formation of this class of highly oxygenated organic hydroperoxides represents a poorly characterized aqueous-phase processing pathway that may lead to enhanced SOA formation and aerosol toxicity. Specifically, the equilibrium constants of α-HHP formation have been determi...

  12. Formation of aqueous-phase α-hydroxyhydroperoxides (α-HHP): potential atmospheric impacts

    OpenAIRE

    Zhao, R.; A. K. Y. Lee; Soong, R; Simpson, A. J.; J. P. D. Abbatt

    2013-01-01

    The focus of this work is on quantifying the degree of the aqueous-phase formation of α-hydroxyhydroperoxides (α-HHPs) via reversible nucleophilic addition of H2O2 to aldehydes. Formation of this class of highly oxygenated organic hydroperoxides represents a poorly characterized aqueous-phase processing pathway that may lead to enhanced SOA formation and aerosol toxicity. Specifically, the equilibrium constants of α-HHP formation have been determined using proton nuclear-magnetic-resonance (1...

  13. Directly Phase-Modulated Light Source

    Science.gov (United States)

    Yuan, Z. L.; Fröhlich, B.; Lucamarini, M.; Roberts, G. L.; Dynes, J. F.; Shields, A. J.

    2016-07-01

    The art of imparting information onto a light wave by optical signal modulation is fundamental to all forms of optical communication. Among many schemes, direct modulation of laser diodes stands out as a simple, robust, and cost-effective method. However, the simultaneous changes in intensity, frequency, and phase have prevented its application in the field of secure quantum communication. Here, we propose and experimentally demonstrate a directly phase-modulated light source which overcomes the main disadvantages associated with direct modulation and is suitable for diverse applications such as coherent communications and quantum cryptography. The source separates the tasks of phase preparation and pulse generation between a pair of semiconductor lasers leading to very pure phase states. Moreover, the cavity-enhanced electro-optic effect enables the first example of subvolt half-wave phase modulation at high signal rates. The source is compact, stable, and versatile, and we show its potential to become the standard transmitter for future quantum communication networks based on attenuated laser pulses.

  14. 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.

  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. Nickel/ruthenium catalyst and method for aqueous phase reactions

    Science.gov (United States)

    Elliott, Douglas C.; Sealock, John L.

    1998-01-01

    A method of hydrogenation using a catalyst in the form of a plurality of porous particles wherein each particle is a support having nickel metal catalytic phase or reduced nickel deposited thereon in a first dispersed phase and an additional ruthenium metal deposited onto the support in a second dispersed phase. The additional ruthenium metal is effective in retarding or reducing agglomeration or sintering of the nickel metal catalytic phase thereby increasing the life time of the catalyst during hydrogenation reactions.

  17. Extraction of peptide tagged cutinase in detergent-based aqueous two-phase systems

    NARCIS (Netherlands)

    Rodenbrock, A.; Selber, K.; Egmond, M.R.; Kula, M.-R.

    2010-01-01

    Detergent-based aqueous two-phase systems have the advantage to require only one auxiliary chemical to induce phase separation above the cloud point. In a systematic study the efficiency of tryptophan-rich peptide tags was investigated to enhance the partitioning of an enzyme to the detergent-rich p

  18. Study on aqueous two-phase systems of the mixture SDS/CTAB surfactants

    Institute of Scientific and Technical Information of China (English)

    LI Ying; CHEN Yah-ming; ZHAO Kong-shuang; Takumi HIKIDA

    2004-01-01

    The phenomenon of two dilute aqueous phases composed of sodium dodecylsulfate (SDS) and cetyltrimethyl ammonium bromide(CTAB) was investigated under various conditions such as concentrations and molarratios of the two surfactants, the addition of sodium chloride and temperature. Vesicles formation was found in theboth phases by TEM image.

  19. 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...

  20. The kinetics and mechanism of an aqueous phase isoprene reaction with hydroxyl radical

    OpenAIRE

    Huang, D.; X. Zhang; Chen, Z M; Zhao, Y.; X. L. Shen

    2011-01-01

    Aqueous phase chemical processes of organic compounds in the atmosphere have received increasing attention, partly due to their potential contribution to the formation of secondary organic aerosol (SOA). Here, we analyzed the aqueous OH-initiated oxidation of isoprene and its reaction products including carbonyl compounds and organic acids, regarding the acidity and temperature as in-cloudy conditions. We also performed a laboratory simulation to improve our understanding of the kinetics and ...

  1. Dissolved plume attenuation with DNAPL source remediation, aqueous decay and volatilization — Analytical solution, model calibration and prediction uncertainty

    Science.gov (United States)

    Parker, Jack C.; Park, Eungyu; Tang, Guoping

    2008-11-01

    A vertically-integrated analytical model for dissolved phase transport is described that considers a time-dependent DNAPL source based on the upscaled dissolution kinetics model of Parker and Park with extensions to consider time-dependent source zone biodecay, partial source mass reduction, and remediation-enhanced source dissolution kinetics. The model also considers spatial variability in aqueous plume decay, which is treated as the sum of aqueous biodecay and volatilization due to diffusive transport and barometric pumping through the unsaturated zone. The model is implemented in Excel/VBA coupled with (1) an inverse solution that utilizes prior information on model parameters and their uncertainty to condition the solution, and (2) an error analysis module that computes parameter covariances and total prediction uncertainty due to regression error and parameter uncertainty. A hypothetical case study is presented to evaluate the feasibility of calibrating the model from limited noisy field data. The results indicate that prediction uncertainty increases significantly over time following calibration, primarily due to propagation of parameter uncertainty. However, differences between the predicted performance of source zone partial mass reduction and the known true performance were reasonably small. Furthermore, a clear difference is observed between the predicted performance for the remedial action scenario versus that for a no-action scenario, which is consistent with the true system behavior. The results suggest that the model formulation can be effectively utilized to assess monitored natural attenuation and source remediation options if careful attention is given to model calibration and prediction uncertainty issues.

  2. Dissolved plume attenuation with DNAPL source remediation, aqueous decay and volatilization--analytical solution, model calibration and prediction uncertainty.

    Science.gov (United States)

    Parker, Jack C; Park, Eungyu; Tang, Guoping

    2008-11-14

    A vertically-integrated analytical model for dissolved phase transport is described that considers a time-dependent DNAPL source based on the upscaled dissolution kinetics model of Parker and Park with extensions to consider time-dependent source zone biodecay, partial source mass reduction, and remediation-enhanced source dissolution kinetics. The model also considers spatial variability in aqueous plume decay, which is treated as the sum of aqueous biodecay and volatilization due to diffusive transport and barometric pumping through the unsaturated zone. The model is implemented in Excel/VBA coupled with (1) an inverse solution that utilizes prior information on model parameters and their uncertainty to condition the solution, and (2) an error analysis module that computes parameter covariances and total prediction uncertainty due to regression error and parameter uncertainty. A hypothetical case study is presented to evaluate the feasibility of calibrating the model from limited noisy field data. The results indicate that prediction uncertainty increases significantly over time following calibration, primarily due to propagation of parameter uncertainty. However, differences between the predicted performance of source zone partial mass reduction and the known true performance were reasonably small. Furthermore, a clear difference is observed between the predicted performance for the remedial action scenario versus that for a no-action scenario, which is consistent with the true system behavior. The results suggest that the model formulation can be effectively utilized to assess monitored natural attenuation and source remediation options if careful attention is given to model calibration and prediction uncertainty issues. PMID:18502537

  3. The role of bio-ethanol in aqueous phase reforming to sustainable hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Tokarev, A.V.; Murzina, E.V.; Eraenen, K.; Murzin, D.Yu. [Aabo Akademi University, Industrial Chemistry and Reaction Engineering, Process Chemistry Centre, Biskopsgatan 8, FIN-20500 Turku/Aabo (Finland); Kirilin, A.V. [Aabo Akademi University, Industrial Chemistry and Reaction Engineering, Process Chemistry Centre, Biskopsgatan 8, FIN-20500 Turku/Aabo (Finland); Zelinsky Institute of Organic Chemistry, Moscow (Russian Federation); Kustov, L.M. [Zelinsky Institute of Organic Chemistry, Moscow (Russian Federation); Mikkola, J.-P. [Aabo Akademi University, Industrial Chemistry and Reaction Engineering, Process Chemistry Centre, Biskopsgatan 8, FIN-20500 Turku/Aabo (Finland); Umeaa University, Technical Chemistry Department of Chemistry, Chemical-Biological Centre, Umeaa (Sweden)

    2010-11-15

    Aqueous Phase Reforming (APR) has during the recent years emerged as a potent, alternative means of processing raw materials of biological origin to component suitable as chemicals and fuel components. In contrary to e.g. steam reforming, aqueous phase reforming bares the promise of lower temperatures in processing which gives rise to potential of reduced energy consumption in the upgrading process itself. Aqueous phase reforming was studied over Pt/Al2O3 at 225 C. Stable catalyst performance and high selectivity was observed. Upon a comparison of two 'bio-alcohols', bio-ethanol and Sorbitol (a sugar alcohol), the latter one is a better feedstock from overall energy utilization viewpoint but the use of it results in a broad range of products. Interestingly, in the case of sorbitol-ethanol mixtures, an improvement in the hydrogen yield was observed. (author)

  4. Liquid-liquid phase separation in mixed organic/inorganic single aqueous aerosol droplets

    OpenAIRE

    Stewart, D J; Cai, C.; Nayler, J.; Preston, T. C.; J. P. Reid; Krieger, U. K.; Marcolli, C.; Zhang, Y H

    2015-01-01

    Direct measurements of the phase separation relative humidity (RH) and morphology of aerosol particles consisting of liquid organic and aqueous inorganic domains are presented. Single droplets of mixed phase composition are captured in a gradient force optical trap, and the evolving size, refractive index (RI), and morphology are characterized by cavity-enhanced Raman spectroscopy. Starting at a RH above the phase separation RH, the trapped particle is dried to lower RH and the transition to ...

  5. 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.

  6. Aqueous organic chemistry in the atmosphere: sources and chemical processing of organic aerosols.

    Science.gov (United States)

    McNeill, V Faye

    2015-02-01

    Over the past decade, it has become clear that aqueous chemical processes occurring in cloud droplets and wet atmospheric particles are an important source of organic atmospheric particulate matter. Reactions of water-soluble volatile (or semivolatile) organic gases (VOCs or SVOCs) in these aqueous media lead to the formation of highly oxidized organic particulate matter (secondary organic aerosol; SOA) and key tracer species, such as organosulfates. These processes are often driven by a combination of anthropogenic and biogenic emissions, and therefore their accurate representation in models is important for effective air quality management. Despite considerable progress, mechanistic understanding of some key aqueous processes is still lacking, and these pathways are incompletely represented in 3D atmospheric chemistry and air quality models. In this article, the concepts, historical context, and current state of the science of aqueous pathways of SOA formation are discussed.

  7. Subcritical hydrothermal liquefaction of barley straw in fresh water and recycled aqueous phase

    DEFF Research Database (Denmark)

    Zhu, Zhe; Toor, Saqib; Rosendahl, Lasse;

    2014-01-01

    addition of recycling aqueous phase in HTL process, it is expected that the amount of the waste water and energy consumption can be reduced. The effect of water recirculation on product yield and properties was investigated in this study. The results showed that bio-oil yield was 34.85 wt% when the barley...... straw was first liquefied in fresh distilled water with the presence of K2CO3 catalyst at 300 C as the reference run. Afterwards, the aqueous phase which is obtained from liquefaction process in the previous run was recycled and used as the reaction medium from the second to the fourth run. With the...

  8. Phase Changes of Monosulfoaluminate in NaCl Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Seyoon Yoon

    2016-05-01

    Full Text Available Monosulfoaluminate (Ca4Al2(SO4(OH12∙6H2O plays an important role in anion binding in Portland cement by exchanging its original interlayer ions (SO42− and OH− with chloride ions. In this study, scanning transmission X-ray microscope (STXM, X-ray absorption near edge structure (XANES spectroscopy, and X-ray diffraction (XRD were used to investigate the phase change of monosulfoaluminate due to its interaction with chloride ions. Pure monosulfoaluminate was synthesized and its powder samples were suspended in 0, 0.1, 1, 3, and 5 M NaCl solutions for seven days. At low chloride concentrations, a partial dissolution of monosulfoaluminate formed ettringite, while, with increasing chloride content, the dissolution process was suppressed. As the NaCl concentration increased, the dominant mechanism of the phase change became ion exchange, resulting in direct phase transformation from monosulfoaluminate to Kuzel’s salt or Friedel’s salt. The phase assemblages of the NaCl-reacted samples were explored using thermodynamic calculations and least-square linear combination (LC fitting of measured XANES spectra. A comprehensive description of the phase change and its dominant mechanism are discussed.

  9. Roles of Mineralogical Phases in Aqueous Carbonation of Steelmaking Slag

    Directory of Open Access Journals (Sweden)

    Huining Zhang

    2016-05-01

    Full Text Available Mineralogical phases of steelmaking slags have significant influences on the carbonation of the slags. In this paper, the effects of temperature and reaction time on the conversion of calcium-related phases and the carbonation degree of a slag sample were studied. The experimental conditions were a liquid-to-solid ratio of 20 mL/g, a carbon dioxide flow rate of 1 L/min and a slag particle size of 38–75 μm. The results show that the optimum carbonation temperature and reaction time are 60 °C and 90 min, respectively, and calcite phase content is about 26.78% while the conversion rates of Ca3Al2O6, CaSiO3, Ca2SiO4 and free CaO are about 40%, 42.46%, 51% and 100%, respectively, and the carbon dioxide sequestration efficiency is about 170 g/kg slag.

  10. Key parameters controlling OH-initiated formation of secondary organic aerosol in the aqueous phase (aqSOA)

    Science.gov (United States)

    Ervens, Barbara; Sorooshian, Armin; Lim, Yong B.; Turpin, Barbara J.

    2014-04-01

    Secondary organic aerosol formation in the aqueous phase of cloud droplets and aerosol particles (aqSOA) might contribute substantially to the total SOA burden and help to explain discrepancies between observed and predicted SOA properties. In order to implement aqSOA formation in models, key processes controlling formation within the multiphase system have to be identified. We explore parameters affecting phase transfer and OH(aq)-initiated aqSOA formation as a function of OH(aq) availability. Box model results suggest OH(aq)-limited photochemical aqSOA formation in cloud water even if aqueous OH(aq) sources are present. This limitation manifests itself as an apparent surface dependence of aqSOA formation. We estimate chemical OH(aq) production fluxes, necessary to establish thermodynamic equilibrium between the phases (based on Henry's law constants) for both cloud and aqueous particles. Estimates show that no (currently known) OH(aq) source in cloud water can remove this limitation, whereas in aerosol water, it might be feasible. Ambient organic mass (oxalate) measurements in stratocumulus clouds as a function of cloud drop surface area and liquid water content exhibit trends similar to model results. These findings support the use of parameterizations of cloud-aqSOA using effective droplet radius rather than liquid water volume or drop surface area. Sensitivity studies suggest that future laboratory studies should explore aqSOA yields in multiphase systems as a function of these parameters and at atmospherically relevant OH(aq) levels. Since aerosol-aqSOA formation significantly depends on OH(aq) availability, parameterizations might be less straightforward, and oxidant (OH) sources within aerosol water emerge as one of the major uncertainties in aerosol-aqSOA formation.

  11. 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.

  12. Chemiluminescence studies between aqueous phase synthesized mercaptosuccinic acid capped cadmium telluride quantum dots and luminol-H2O2

    Science.gov (United States)

    Kaviyarasan, Kulandaivelu; Anandan, Sambandam; Mangalaraja, Ramalinga Viswanathan; Asiri, Abdullah M.; Wu, Jerry J.

    2016-08-01

    Mercaptosuccinic acid capped Cadmium telluride quantum dots have been successfully synthesized via aqueous phase method. The products were well characterized by a number of analytical techniques, including FT-IR, XRD, HRTEM, and a corrected particle size analysis by the statistical treatment of several AFM measurements. Chemiluminescence experiments were performed to explore the resonance energy transfer between chemiluminescence donor (luminol-H2O2 system) and acceptor CdTe QDs. The combination of such donor and acceptor dramatically reduce the fluorescence while compared to pristine CdTe QDs without any exciting light source, which is due to the occurrence of chemiluminescence resonance energy transfer (CRET) processes.

  13. Chemiluminescence studies between aqueous phase synthesized mercaptosuccinic acid capped cadmium telluride quantum dots and luminol-H2O2.

    Science.gov (United States)

    Kaviyarasan, Kulandaivelu; Anandan, Sambandam; Mangalaraja, Ramalinga Viswanathan; Asiri, Abdullah M; Wu, Jerry J

    2016-08-01

    Mercaptosuccinic acid capped Cadmium telluride quantum dots have been successfully synthesized via aqueous phase method. The products were well characterized by a number of analytical techniques, including FT-IR, XRD, HRTEM, and a corrected particle size analysis by the statistical treatment of several AFM measurements. Chemiluminescence experiments were performed to explore the resonance energy transfer between chemiluminescence donor (luminol-H2O2 system) and acceptor CdTe QDs. The combination of such donor and acceptor dramatically reduce the fluorescence while compared to pristine CdTe QDs without any exciting light source, which is due to the occurrence of chemiluminescence resonance energy transfer (CRET) processes. PMID:27131144

  14. Gas-Phase Oxidation of Aqueous Ethanol by Nanoparticle Vanadia/Anatase Catalysts

    DEFF Research Database (Denmark)

    Jørgensen, Betina; Kristensen, Steffen Buus; Kunov-Kruse, Andreas Jonas;

    2009-01-01

    The gas-phase oxidation of aqueous ethanol with dioxygen has been examined with a new nanoparticle V2O5/TiO2 catalyst. Product selectivity could to a large extent be controlled by small alterations of reaction parameters, allowing production of acetaldehyde at a selectivity higher than 90%, near...

  15. Aqueous-phase hydrogenation of acetic acid over transition metal catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Olcay, Hakan [University of Massachusetts, Amherst; Xu, Lijun [ORNL; Xu, Ye [ORNL; Huber, George [University of Massachusetts, Amherst

    2010-01-01

    Catalytic hydrogenation of acetic acid to ethanol has been carried out in aqueous phase on several metals, with ruthenium being the most active and selective. DFT calculations suggest that the initial CO bond scission yielding acetyl is the key step and that the intrinsic reactivity of the metals accounts for the observed activity.

  16. Dynamic speciation analysis of atrazine in aqueous latex nanoparticle dispersions using solid phase microextraction (SPME)

    NARCIS (Netherlands)

    Benhabib, K.; Town, R.M.; Leeuwen, van H.P.

    2009-01-01

    Solid phase microextraction (SPME) is applied in the dynamic speciation analysis of the pesticide atrazine in an aqueous medium containing sorbing latex nanoparticles. It is found that the overall rate of extraction of the analyte is faster than in the absence of nanoparticles and governed by the co

  17. Effect of initial nickel particle size on stability of nickel catalysts for aqueous phase reforming

    NARCIS (Netherlands)

    Haasterecht, Van Tomas; Swart, Marten; Jong, De Krijn P.; Bitter, J.H.

    2016-01-01

    The deactivation behavior by crystallite growth of nickel nanoparticles on various supports (carbon nanofibers, zirconia, SiC, α-Al2O3 and γ-Al2O3) was investigated in the aqueous phase reforming of ethylene glycol. Supported Ni catalysts of ∼10 wt% were prepared by impregnation of carbon nanofibers

  18. Lignin solubilization and aqueous phase reforming for the production of aromatic chemicals and hydrogen

    NARCIS (Netherlands)

    Zakzeski, J.; Weckhuysen, B.M.

    2011-01-01

    The solubilization and aqueous phase reforming of lignin, including kraft, soda, and alcell lignin along with sugarcane bagasse, at low temperatures (T≤498 K) and pressures (P≤29 bar) is reported for the first time for the production of aromatic chemicals and hydrogen. Analysis of lignin model compo

  19. Correlation and Prediction of Thermal Properties and Phase Behaviour for a Class of Aqueous Electrolyte Systems

    DEFF Research Database (Denmark)

    Thomsen, Kaj; Rasmussen, Peter; Gani, Rafiqul

    1996-01-01

    An extended UNIQUAC model is used to describe phase behaviour (VLE, SLE) and thermal properties (heat of mixing, heat capacity) for aqueous solutions containing ions like (Na+, K+, H+) (Cl-, NO3-, SO42-, OH-, CO3-). A linear temperature dependence of the binary interaction parameters allows good...

  20. Multiscale approach to CO2 hydrate formation in aqueous solution: phase field theory and molecular dynamics. Nucleation and growth.

    Science.gov (United States)

    Tegze, György; Pusztai, Tamás; Tóth, Gyula; Gránásy, László; Svandal, Atle; Buanes, Trygve; Kuznetsova, Tatyana; Kvamme, Bjorn

    2006-06-21

    A phase field theory with model parameters evaluated from atomistic simulations/experiments is applied to predict the nucleation and growth rates of solid CO(2) hydrate in aqueous solutions under conditions typical to underwater natural gas hydrate reservoirs. It is shown that under practical conditions a homogeneous nucleation of the hydrate phase can be ruled out. The growth rate of CO(2) hydrate dendrites has been determined from phase field simulations as a function of composition while using a physical interface thickness (0.85+/-0.07 nm) evaluated from molecular dynamics simulations. The growth rate extrapolated to realistic supersaturations is about three orders of magnitude larger than the respective experimental observation. A possible origin of the discrepancy is discussed. It is suggested that a kinetic barrier reflecting the difficulties in building the complex crystal structure is the most probable source of the deviations.

  1. 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...

  2. 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...

  3. Toward stable nickel catalysts for aqueous phase reforming of biomass-derived feedstock under reducing and alkaline conditions

    NARCIS (Netherlands)

    Haasterecht, van T.; Ludding, C.C.I.; Jong, de K.P.; Bitter, J.H.

    2014-01-01

    Nickel nanoparticles supported on carbon nanofibers (CNF) can be stabilized in aqueous phase processes at elevated temperatures and pressures by tuning the reaction conditions to control Ni oxidation and leaching. As a showcase, Ni/CNF was used for the production of hydrogen via aqueous phase reform

  4. Aqueous-phase story of isoprene - A mini-review and reaction with HONO

    Science.gov (United States)

    Rudziński, Krzysztof J.; Szmigielski, Rafał; Kuznietsova, Inna; Wach, Paulina; Staszek, Dorota

    2016-04-01

    Isoprene is a major biogenic hydrocarbon emitted to the atmosphere and a well-recognized player in atmospheric chemistry, formation of secondary organic aerosol and air quality. Most of the scientific work on isoprene has focused on the gas-phase and smog chamber processing while direct aqueous chemistry has escaped the major attention because physical solubility of isoprene in water is low. Therefore, this work recollects the results of genuine research carried on atmospherically relevant aqueous-phase transformations of isoprene. It clearly shows that isoprene dissolves in water and reacts in aqueous solutions with common atmospheric oxidants such as hydrogen peroxide, ozone, hydroxyl radicals, sulfate radicals and sulfite radicals. The reactions take place in the bulk of solutions or on the gas-liquid interfaces and often are acid-catalyzed and/or enhanced by light. The review is appended by an experimental study of the aqueous-phase reaction of isoprene with nitrous acid (HONO). The decay of isoprene and formation of new products are demonstrated. The tentative chemical mechanism of the reaction is suggested, which starts with slow decomposition of HONO to NO2 and NO. The aqueous chemistry of isoprene explains the formation of a few tropospheric components identified by scientists yet considered of unknown origin. The reaction of isoprene with sulfate radicals explains formation of the MW 182 organosulfate found in ambient aerosol and rainwater while the reaction of isoprene with HONO explains formation of the MW 129 and MW 229 nitroorganic compounds identified in rainwater. Thus, aqueous transformations of isoprene should not be neglected without evidence but rather considered and evaluated in modeling of atmospheric chemical processes even if alternative and apparently dominant heterogeneous pathways of isoprene transformation, dry or wet, are demonstrated.

  5. Explicit modeling of volatile organic compounds partitioning in the atmospheric aqueous phase

    Directory of Open Access Journals (Sweden)

    C. Mouchel-Vallon

    2012-09-01

    Full Text Available The gas phase oxidation of organic species is a multigenerational process involving a large number of secondary compounds. Most secondary organic species are water-soluble multifunctional oxygenated molecules. The fully explicit chemical mechanism GECKO-A (Generator of Explicit Chemistry and Kinetics of Organics in the Atmosphere is used to describe the oxidation of organics in the gas phase and their mass transfer to the aqueous phase. The oxidation of three hydrocarbons of atmospheric interest (isoprene, octane and α-pinene is investigated for various NOx conditions. The simulated oxidative trajectories are examined in a new two dimensional space defined by the mean oxidation state and the solubility. The amount of dissolved organic matter was found to be very low (<2% under a water content typical of deliquescent aerosols. For cloud water content, 50% (isoprene oxidation to 70% (octane oxidation of the carbon atoms are found in the aqueous phase after the removal of the parent hydrocarbons for low NOx conditions. For high NOx conditions, this ratio is only 5% in the isoprene oxidation case, but remains large for α-pinene and octane oxidation cases (40% and 60%, respectively. Although the model does not yet include chemical reactions in the aqueous phase, much of this dissolved organic matter should be processed in cloud drops and modify both oxidation rates and the speciation of organic species.

  6. The kinetics and mechanism of an aqueous phase isoprene reaction with hydroxyl radical

    Directory of Open Access Journals (Sweden)

    D. Huang

    2011-08-01

    Full Text Available Aqueous phase chemical processes of organic compounds in the atmosphere have received increasing attention, partly due to their potential contribution to the formation of secondary organic aerosol (SOA. Here, we analyzed the aqueous OH-initiated oxidation of isoprene and its reaction products including carbonyl compounds and organic acids, regarding the acidity and temperature as in-cloudy conditions. We also performed a laboratory simulation to improve our understanding of the kinetics and mechanisms for the products of aqueous isoprene oxidation that are significant precursors of SOA; these included methacrolein (MACR, methyl vinyl ketone (MVK, methyl glyoxal (MG, and glyoxal (GL. We used a novel chemical titration method to monitor the concentration of isoprene in the aqueous phase. We used a box model to interpret the mechanistic differences between aqueous and gas phase OH radical-initiated isoprene oxidations. Our results were the first demonstration of the rate constant for the reaction between isoprene and OH radical in water, 1.2 ± 0.4 × 1010 M−1 s−1 at 283 K. Molar yields were determined based on consumed isoprene. Of note, the ratio of the yields of MVK (24.1 ± 0.8 % to MACR (10.9 ± 1.1% in the aqueous phase isoprene oxidation was approximately double that observed for the corresponding gas phase reaction. We hypothesized that this might be explained by a water-induced enhancement in the self-reaction of a hydroxy isoprene peroxyl radical (HOCH2C(CH3(O2CH = CH2 produced in the aqueous reaction. The observed yields for MG and GL were 11.4 ± 0.3 % and 3.8 ± 0.1 %, respectively. Model simulations indicated that several potential pathways may contribute to the formation of MG and GL. Finally, oxalic acid increased steadily throughout the course of the study, even after isoprene was consumed completely. The observed yield of oxalic acid was 26.2 ± 0

  7. Preparation,characterization and properties studies of quinine-imprinted polymer in the aqueous phase

    Institute of Scientific and Technical Information of China (English)

    He Jianfeng; Liu Lan; Yang Guilan; Deng Qinying

    2006-01-01

    The uniform-sized spherical molecularly imprinted polymers were successfully prepared through molecular imprinting technology by two-step seed swelling and mini-emulsion polymerization in the aqueous condition using quinine as template molecules and methacrylic acid (MAA)as functional monomer.The polymers were characterized by IR spectra,thermal-weight analysis,scanning electron microscope and laser particle size analysis.The properties of imprinted polymers were investigated in different organic phases and aqueous media.In the organic media,results suggested that polar interactions(hydrogen bonding,ionic interactions)between acidic monomer/polymer and template molecules are mainly responsible for the binding and recognition;whereas in the aqueous medium,a considerable recognition effect was also obtained where the ionic(electrostatic)interaction and hydrophobic interaction play an important role.The experiments of binding different substrates indicated that the MIPs possessed an excellent rebinding ability and inherent selectivity to quinine.

  8. Fullerene-containing phases obtained from aqueous dispersions of carbon nanoparticles

    Science.gov (United States)

    Rozhkov, S. P.; Kovalevskii, V. V.; Rozhkova, N. N.

    2007-06-01

    The hydration of fullerenes and shungite carbon nanoclusters in aqueous dispersions at various carbon concentrations is studied on frozen samples by EPR with spin probes. It is found that, for stable dispersions of both substances (at carbon concentrations of 0.1 mg/ml), the probe rotation frequency versus 1/T dependences exhibit a plateau in the range 243 257 K, which is probably associated with the peculiarities of freezing of water localized near hydrophobic structures of carbon nanoclusters. Solid phases isolated from supersaturated aqueous dispersions of fullerenes and shungites by slow evaporation of water at temperatures higher than 0°C are examines by electron diffraction and electron microscopy. It is established that obtained films of fullerenes contain at least two phases: fullerite with a face-centered cubic lattice and a phase similar in interplanar spacing and radically different in distribution of intensities of diffraction peaks. It is concluded that this phase is formed by the interaction of fullerenes and water (an analogous phase is found in shungite carbon films). It is found that the morphology of the new crystal phase is characterized by globules of size 20 to 70 nm, for fullerenes, and 10 to 400 nm for shungites. It is established that processes of crystallization of fullerites and fullerene-containing phases are very sensitive to temperature: a decrease in the temperature (within the range from 40 to 1°C) is accompanied by an increase in the new phase content.

  9. Solid phase precipitates in (Zr,Th)-OH-(oxalate, malonate) ternary aqueous system

    Energy Technology Data Exchange (ETDEWEB)

    Kobayashi, T.; Sasaki, T.; Takagi, I.; Moriyama, H. [Kyoto Univ. (Japan). Dept. of Nuclear Engineering

    2009-07-01

    The solubility-limiting solid phases in the ternary aqueous systems of Zr(IV)/OH/oxalate, Zr(IV)/OH/malonate, Th(IV)/OH/oxalate and Th(IV)/OH/malonate were characterized by elemental analysis, X-ray diffraction, thermogravimetric analysis and differential thermal analysis. The ternary solid phase of M(IV)/OH/carboxylate was observed to form, even under acidic conditions, depending on the pH and the concentration of carboxylate ligand. In the presence of a large excess of carboxylic acid, however; the binary M(IV)-carboxylate solid phase formed. (orig.)

  10. Phases confirmation of cloudy Silwet L-77 aqueous solution by dielectric relaxation spectroscopy

    Institute of Scientific and Technical Information of China (English)

    Wei

    2010-01-01

    The phase transition of Silwet L-77 (a kind of siloxane surfactant) dilute aqueous solution with temperature was investigated by dielectric relaxation spectroscopy. In the initial heating process, a dielectric relaxation was found at about 106 Hz, which was considered as the interface polarization ascribed to the interface between water and liquid phases (Wand L1). With the temperature increasing further, a new dielectric relaxation was observed at about 104 Hz, which was assigned to the appearance of liquid crystal phase (Lα). According to the dielectric parameters fitted by Cole-Cole equation, the coexistence temperature of W, L1 and Lα was determined at about 37.0℃.

  11. Phase transfer of platinum nanoparticles from aqueous to organic solutions using fatty amine molecules

    Indian Academy of Sciences (India)

    Ashavani Kumar; Hrushikesh M Joshi; Anandrao B Mandale; Rajendra Srivastava; Suguna D Adyanthaya; Renu Pasricha; Murali Sastry

    2004-08-01

    In this report we demonstrate a simple process based on amine chemistry for the phase transfer of platinum nanoparticles from an aqueous to an organic solution. The phase transfer was accomplished by vigorous shaking of a biphasic mixture of platinum nanoparticles synthesised in an aqueous medium and octadecylamine (ODA) in hexane. During shaking of the biphasic mixture, the aqueous platinum nanoparticles complex via either coordination bond formation or weak covalent interaction with the ODA molecules present in the organic phase. This process renders the nanoparticles sufficiently hydrophobic and dispersible in the organic phase. The ODA-stabilised platinum nanoparticles could be separated out from hexane in the form of a powder that is readily redispersible in weakly polar and nonpolar organic solvents. The ODA-capped platinum nanoparticles show high catalytic activity in hydrogenation reactions and this is demonstrated in the efficient conversion of styrene to ethyl benzene. The nature of binding of the ODA molecules to the platinum nanoparticles surface was characterised by thermogravimetry, transmission electron microscopy (TEM), X-ray photoemission spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR).

  12. Towards a more detailed description of tropospheric aqueous phase organic chemistry: CAPRAM 3.0

    Science.gov (United States)

    Herrmann, H.; Tilgner, A.; Barzaghi, P.; Majdik, Z.; Gligorovski, S.; Poulain, L.; Monod, A.

    CAPRAM 3.0 is the latest development of the chemical aqueous phase radical mechanism (CAPRAM) series which is incorporating CAPRAM 2.4 (Ervens et al., 2003a, Journal of Geophysical Research—Atmospheres 108) and a new extended reaction mechanism for atmospherically relevant hydrocarbons containing more than two and up to six carbon atoms. The chemistry of organics containing three and four carbon atoms is now described in detail. Almost 400 new reactions are now implemented considering the chemistry of organic compounds containing different functional groups, i.e. alcohols, carbonyl compounds, mono- and dicarboxylic acids, polyfunctional compounds as well as some esters and one heterocyclic compound. The aqueous chemistry has been coupled to the gas phase mechanism RACM (regional atmospheric chemistry modeling) (Stockwell et al., 1997, Journal of Geophysical Research—Atmpspheres 102, 25847-25879), and phase exchange is treated using the resistance model of Schwartz (1986. In: Jaeschke, W. (Ed.), Chemistry of Multiphase Atmospheric Systems, NATO ASI Series, Springer, Berlin, pp. 415-471). The CAPRAM remote scenario which was chosen as the standard scenario showed that the introduction of the higher organic chemistry has a relevant influence on the standard subsystems. The diurnal peak concentration of OH radical in the droplets decreases with about 40% and the reactions of OH with hydrocarbons containing 3 or 4 carbon atoms account for about 10% out of the total sinks of OH in the droplets. A slightly stronger acidification of the aqueous phase in comparison to CAPRAM 2.4 is observed. The simulations for the standard scenario showed that there is an increase of organic mass within the droplets where the organic compounds containing 4 carbon atoms represent the 67.5% of the total mass, whereas in the urban and in the marine scenario the contribution of two carbon atom compounds is dominating. The formation and accumulation of substituted mono- and dicarboxylic

  13. Impact of backmixing of the aqueous phase on two-component rare earth separation process

    Institute of Scientific and Technical Information of China (English)

    WU Sheng; CHENG Fuxiang; LIAO Chunsheng; YAN Chunhua

    2013-01-01

    Solvent extraction based on mixer-settler is the major industrial method of rare earth (RE) separation.In the mixer-settler extraction process,due to the insufficient settling time in normal circumstances,backmixing of the aqueous phase could have significant impact on the process of RE extraction separation.Therefore on the basis of the extraction equilibrium and mass balance of the mixer-settler extraction process,here we developed a mathematic expression of the aqueous phase backmixing in a two-component separation process,and obtained a quantitative analysis of the backmixing effect on the purification process by the approximations according to certain hypotheses.Two extraction systems of La/Ce and Pr/Nd separation were chosen as the examples to analyze the backmixing effect,and the results showed that the aqueous backmixing had greater influence in the scrubbing segment than in the extraction segment,especially in the system with a high separation factor such as La/Ce separation.Therefore it was suggested that the aqueous backmixing effect should be well attended in the design and application of RE extraction separation.

  14. Discovery of a tetracontinuous, aqueous lyotropic network phase with unusual 3D-hexagonal symmetry.

    Science.gov (United States)

    Sorenson, Gregory P; Schmitt, Adam K; Mahanthappa, Mahesh K

    2014-11-01

    Network phase aqueous lyotropic liquid crystals (LLCs) are technologically useful materials with myriad applications in chemistry, biology, and materials science, which stem from their structurally periodic aqueous and hydrophobic nanodomains (∼0.7-5.0 nm in diameter) that are lined with well-defined chemical functionalities. The exclusive observation of bicontinuous cubic network phase LLCs (e.g., double gyroid, double diamond, and primitive phases) has fueled speculations that all stable LLC network phases must exhibit cubic symmetry. Herein, we describe the self-assembly behavior of a simple aliphatic gemini surfactant that forms the first example of a triply periodic network phase LLC with the 3D-hexagonal symmetry P63/mcm (space group #193). This normal, tetracontinuous 3D-hexagonal network LLC phase HI(193) partitions space into four continuous and interpenetrating, yet non-intersecting volumes. This discovery directly demonstrates that the gemini amphiphile platform furnishes a rational strategy for discovering and stabilizing new, three-dimensionally periodic multiply continuous network phase LLCs with variable symmetries and potentially new applications. PMID:25182008

  15. The separation and analysis of symmetric and asymmetric dimethylarginine and other hydrophilic isobaric compounds using aqueous normal phase chromatography.

    Science.gov (United States)

    Pesek, Joseph J; Matyksa, Maria T; Modereger, Brent; Hasbun, Alejandra; Phan, Vy T; Mehr, Zahra; Guzman, Mariano; Watanable, Seiichiro

    2016-04-01

    Two biologically important compounds with clinical relevance, asymmetric dimethylarginine and symmetric dimethylarginine, are analyzed using aqueous normal phase chromatography on silica hydride-based columns. Two different stationary phases were tested, a commercially available Diamond Hydride™ and a 2-acrylamido-2-methylpropane sulfonic acid experimental column. Two types of analytical protocols were investigated: analysis of the compounds when separation was achieved and analysis of the compounds with partial chromatographic separation. Urine samples from tuberculosis patients were tested for levels of asymmetric and symmetric dimethylarginine. The mass spectrometric technique of in-source fragmentation that can provide data similar to a tandem mass analyzer was evaluated as a means of identification and quantitation of the two compounds when complete separation is not achieved. This same protocol was also evaluated for two other isobaric compounds, glucose-1 and glucose-6 phohsphate, and leucine and isoleucine.

  16. Large-scale synthesis of CdTe quantum dots in aqueous phase

    International Nuclear Information System (INIS)

    In this paper, we present the systematically experimental results on the influence of pH of the reaction medium, molar ratio of the precursors on the synthesis in aqueous phase of CdTe quantum dots (QDs) and CdTe/CdS QDs with core/shell structure. Under optimal synthesis conditions, water-soluble CdTe and CdTe/CdS QDs has been prepared that exhibit very strong photoluminescence peaking in the spectral range between 520 nm and 650 nm with narrow full width at half maximum (∼ 32 nm in the short-wavelength emission case); depending on the emission range, most samples however exhibit the high luminescence quantum yields (∼ 40%). Moreover, the synthesis in aqueous phase shows some additional advantages: it is possible to prepare high quality CdTe QDs in large-scale (up to gram/reaction) with low cost, less toxic and short production time. (author)

  17. Metallic and semiconducting carbon nanotubes separation using an aqueous two-phase separation technique: a review

    Science.gov (United States)

    Tang, Malcolm S. Y.; Ng, Eng-Poh; Juan, Joon Ching; Ooi, Chien Wei; Ling, Tau Chuan; Woon, Kai Lin; Loke Show, Pau

    2016-08-01

    It is known that carbon nanotubes show desirable physical and chemical properties with a wide array of potential applications. Nonetheless, their potential has been hampered by the difficulties in acquiring high purity, chiral-specific tubes. Considerable advancement has been made in terms of the purification of carbon nanotubes, for instance chemical oxidation, physical separation, and myriad combinations of physical and chemical methods. The aqueous two-phase separation technique has recently been demonstrated to be able to sort carbon nanotubes based on their chirality. The technique requires low cost polymers and salt, and is able to sort the tubes based on their diameter as well as metallicity. In this review, we aim to provide a review that could stimulate innovative thought on the progress of a carbon nanotubes sorting method using the aqueous two-phase separation method, and present possible future work and an outlook that could enhance the methodology.

  18. Heterogeneous Catalytic Conversion of Biobased Chemicals into Liquid Fuels in the Aqueous Phase.

    Science.gov (United States)

    Wu, Kejing; Wu, Yulong; Chen, Yu; Chen, Hao; Wang, Jianlong; Yang, Mingde

    2016-06-22

    Different biobased chemicals are produced during the conversion of biomass into fuels through various feasible technologies (e.g., hydrolysis, hydrothermal liquefaction, and pyrolysis). The challenge of transforming these biobased chemicals with high hydrophilicity is ascribed to the high water content of the feedstock and the inevitable formation of water. Therefore, aqueous-phase processing is an interesting technology for the heterogeneous catalytic conversion of biobased chemicals. Different reactions, such as dehydration, isomerization, aldol condensation, ketonization, and hydrogenation, are applied for the conversion of sugars, furfural/hydroxymethylfurfural, acids, phenolics, and so on over heterogeneous catalysts. The activity, stability, and reusability of the heterogeneous catalysts in water are summarized, and deactivation processes and several strategies are introduced to improve the stability of heterogeneous catalysts in the aqueous phase. PMID:27158985

  19. Maillard Chemistry in Clouds and Aqueous Aerosol As a Source of Atmospheric Humic-Like Substances.

    Science.gov (United States)

    Hawkins, Lelia N; Lemire, Amanda N; Galloway, Melissa M; Corrigan, Ashley L; Turley, Jacob J; Espelien, Brenna M; De Haan, David O

    2016-07-19

    The reported optical, physical, and chemical properties of aqueous Maillard reaction mixtures of small aldehydes (glyoxal, methylglyoxal, and glycolaldehyde) with ammonium sulfate and amines are compared with those of aqueous extracts of ambient aerosol (water-soluble organic carbon, WSOC) and the humic-like substances (HULIS) fraction of WSOC. Using a combination of new and previously published measurements, we examine fluorescence, X-ray absorbance, UV/vis, and IR spectra, complex refractive indices, (1)H and (13)C NMR spectra, thermograms, aerosol and electrospray ionization mass spectra, surface activity, and hygroscopicity. Atmospheric WSOC and HULIS encompass a range of properties, but in almost every case aqueous aldehyde-amine reaction mixtures are squarely within this range. Notable exceptions are the higher UV/visible absorbance wavelength dependence (Angström coefficients) observed for methylglyoxal reaction mixtures, the lack of surface activity of glyoxal reaction mixtures, and the higher N/C ratios of aldehyde-amine reaction products relative to atmospheric WSOC and HULIS extracts. The overall optical, physical, and chemical similarities are consistent with, but not demonstrative of, Maillard chemistry being a significant secondary source of atmospheric HULIS. However, the higher N/C ratios of aldehyde-amine reaction products limits the source strength to ≤50% of atmospheric HULIS, assuming that other sources of HULIS incorporate only negligible quantities of nitrogen. PMID:27227348

  20. 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...

  1. Ultradry Carbon Dioxide-in-Water Foams with Viscoelastic Aqueous Phases.

    Science.gov (United States)

    Xue, Zheng; Worthen, Andrew J; Da, Chang; Qajar, Ali; Ketchum, Isaiah Robert; Alzobaidi, Shehab; Huh, Chun; Prodanović, Maša; Johnston, Keith P

    2016-01-12

    For foams with ultra low water contents, the capillary pressure is very large and induces rapid drainage that destabilizes the aqueous lamellae between the gas bubbles. However, we show that high-pressure CO2-in-water foams can be stabilized with a viscoelastic aqueous phase composed of entangled wormlike micelles, even for extremely high CO2 volume fractions ϕ of 0.95 to 0.98; the viscosity of these ultradry foams increased by up to 3-4-fold, reaching more than 100 cP relative to foams formed with conventional low viscosity aqueous phases. The foam morphology consisted of fine ∼20 μm polyhedral-shaped CO2 bubbles that were stable for hours. The wormlike micelles were formed by mixing anionic sodium lauryl ether sulfate (SLES) with salt and a protonated cationic surfactant, as shown by cryogenic transmission electron microscopy (cryo-TEM) and large values of the zero-shear viscosity and the dynamic storage and loss moduli. With the highly viscous continuous aqueous phases, the foam lamella drainage rates were low, as corroborated by confocal microscopy. The preservation of viscous thick lamellae resulted in lower rates of Ostwald ripening relative to conventional foams as shown by high-pressure optical microscopy. The ability to stabilize viscous ultra high internal phase foams is expected to find utility in various practical applications, including nearly "waterless" fracturing fluids for recovery of oil and gas in shale, offering the possibility of a massive reduction in the amount of wastewater. PMID:26666311

  2. REMOVAL OF METHYLENE BLUE FROM AQUEOUS PHASE BY PRETREATED WALNUT SHELL IN A PACKED COLUMN

    OpenAIRE

    A.A. Nazari-Moghaddam; Najafpour, G.D.; A.A. Ghoeyshi; M Mohammadi; harif Hussein Sharif Zein

    2010-01-01

    Methylene blue (MB) adsorption from aqueous phase was investigated. Pretreated walnut shell, as adsorbent was used. Experiments were conducted in a batch system for determination of sorption equilibria and then the data were incorporated in a packed column for the removal of MB from synthetic wastewater. The generated wastewater was contained 4 mg/l of MB. The wastewater was pumped through the column with flow rate of 18 ml/min and the effluent samples were collected. The effect of influent M...

  3. 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.

  4. Drowning-out crystallisation of sodium sulphate using aqueous two-phase systems.

    Science.gov (United States)

    Taboada, M E; Graber, T A; Asenjo, J A; Andrews, B A

    2000-06-23

    A novel method to obtain crystals of pure, anhydrous salt, using aqueous two-phase systems was studied. A concentrated salt solution is mixed with polyethylene glycol (PEG), upon which three phases are formed: salt crystals, a PEG-rich liquid and a salt-rich liquid. After removal of the solid salt, a two-phase system is obtained. Both liquid phases are recycled, allowing the design of a continuous process, which could be exploited industrially. The phase diagram of the system water-Na2SO4-PEG 3350 at 28 degrees C was used. Several process alternatives are proposed and their economic potential is discussed. The process steps needed to produce sodium sulphate crystals include mixing, crystallisation, settling and, optionally, evaporation of water. The yield of sodium sulphate increases dramatically if an evaporation step is used. PMID:10942277

  5. Hydrothermal upgrading of algae paste: Inorganics and recycling potential in the aqueous phase.

    Science.gov (United States)

    Patel, Bhavish; Guo, Miao; Chong, Chinglih; Sarudin, Syazwani Hj Mat; Hellgardt, Klaus

    2016-10-15

    Hydrothermal Liquefaction (HTL) for algal biomass conversion is a promising technology capable of producing high yields of biocrude as well as partitioning even higher quantity of nutrients in the aqueous phase. To assess the feasibility of utilizing the aqueous phase, HTL of Nannochloropsis sp. was carried out in the temperature range of 275 to 350°C and Residence Times (RT) ranging between 5 and 60min The effect of reaction conditions on the NO3(-),PO4(3-),SO4(2-),Cl(-),Na(+),andK(+) ions as well as Chemical Oxygen Demand (COD) and pH was investigated with view of recycling the aqueous phase for either cultivation or energy generation via Anaerobic Digestion (AD), quantified via Lifecycle Assessment (LCA). It addition to substantial nutrient partitioning at short RT, an increase in alkalinity to almost pH10 and decrease in COD at longer RT was observed. The LCA investigation found reaction conditions of 275°C/30min and 350°C/10min to be most suitable for nutrient and energy recovery but both processing routes offer environmental benefit at all reaction conditions, however recycling for cultivation has marginally better environmental credentials compared to AD. PMID:27318079

  6. Phase and Frequency Locked Magnetrons for SRF Sources

    Energy Technology Data Exchange (ETDEWEB)

    Neubauer, M.; Johnson, R.P.; /Muons Inc., Batavia; Popovic, M.; Moretti, A.; /Fermilab

    2009-05-01

    Magnetrons are low-cost highly-efficient microwave sources, but they have several limitations, primarily centered about the phase and frequency stability of their output. When the stability requirements are low, such as for medical accelerators or kitchen ovens, magnetrons are the very efficient power source of choice. But for high energy accelerators, because of the need for frequency and phase stability - proton accelerators need 1-2 degrees source phase stability, and electron accelerators need .1-.2 degrees of phase stability - they have rarely been used. We describe a novel variable frequency cavity technique which will be utilized to phase and frequency lock magnetrons.

  7. Purification of Active Myrosinase from Plants by Aqueous Two-Phase Counter-Current Chromatography

    Science.gov (United States)

    Wade, Kristina L.; Ito, Yoichiro; Ramarathnam, Aarthi; Holtzclaw, W. David; Fahey, Jed W.

    2014-01-01

    Introduction Myrosinase (thioglucoside glucohydrolase; E.C. 3.2.1.147), is a plant enzyme of increasing interest and importance to the biomedical community. Myrosinase catalyses the formation of isothiocyanates such as sulforaphane (frombroccoli) and 4-(α-l-rhamnopyranosyloxy)benzyl isothiocyanate (from moringa), which are potent inducers of the cytoprotective phase-2 response in humans, by hydrolysis of their abundant glucosinolate (β-thioglucoside N-hydroxysulphate) precursors. Objective To develop an aqueous two-phase counter-current chromatography (CCC) system for the rapid, three-step purification of catalytically active myrosinase. Methods A high-concentration potassium phosphate and polyethylene glycol biphasic aqueous two-phase system (ATPS) is used with a newly developed CCC configuration that utilises spiral-wound, flat-twisted tubing (with an ovoid cross-section). Results Making the initial crude plant extract directly in the ATPS and injecting only the lower phase permitted highly selective partitioning of the myrosinase complex before a short chromatography on a spiral disk CCC. Optimum phase retention and separation of myrosinase from other plant proteins afforded a 60-fold purification. Conclusion Catalytically active myrosinase is purified from 3-day broccoli sprouts, 7-day daikon sprouts, mustard seeds and the leaves of field-grown moringa trees, in a CCC system that is predictably scalable. PMID:25130502

  8. Sponge Phases and Nanoparticle Dispersions in Aqueous Mixtures of Mono- and Diglycerides.

    Science.gov (United States)

    Valldeperas, Maria; Wiśniewska, Małgorzata; Ram-On, Maor; Kesselman, Ellina; Danino, Dganit; Nylander, Tommy; Barauskas, Justas

    2016-08-30

    The lipid liquid crystalline sponge phase (L3) has the advantages that it is a nanoscopically bicontinuous bilayer network able to accommodate large amounts of water and it is easy to manipulate due to its fluidity. This paper reports on the detailed characterization of L3 phases with water channels large enough to encapsulate bioactive macromolecules such as proteins. The aqueous phase behavior of a novel lipid mixture system, consisting of diglycerol monooleate (DGMO), and a mixture of mono-, di- and triglycerides (Capmul GMO-50) was studied. In addition, sponge-like nanoparticles (NPs) stabilized by Polysorbate 80 (P80) were prepared based on the DGMO/GMO-50 system, and their structure was correlated with the phase behavior of the corresponding bulk system. These NPs were characterized by dynamic light scattering (DLS), cryo-transmission electron microscopy (Cryo-TEM) and small angle X-ray scattering (SAXS) to determine their size, shape, and inner structure as a function of the DGMO/GMO-50 ratio. In addition, the effect of P80 as stabilizer was investigated. We found that the NPs have aqueous pores with diameters up to 13 nm, similar to the ones in the bulk phase.

  9. Sponge Phases and Nanoparticle Dispersions in Aqueous Mixtures of Mono- and Diglycerides.

    Science.gov (United States)

    Valldeperas, Maria; Wiśniewska, Małgorzata; Ram-On, Maor; Kesselman, Ellina; Danino, Dganit; Nylander, Tommy; Barauskas, Justas

    2016-08-30

    The lipid liquid crystalline sponge phase (L3) has the advantages that it is a nanoscopically bicontinuous bilayer network able to accommodate large amounts of water and it is easy to manipulate due to its fluidity. This paper reports on the detailed characterization of L3 phases with water channels large enough to encapsulate bioactive macromolecules such as proteins. The aqueous phase behavior of a novel lipid mixture system, consisting of diglycerol monooleate (DGMO), and a mixture of mono-, di- and triglycerides (Capmul GMO-50) was studied. In addition, sponge-like nanoparticles (NPs) stabilized by Polysorbate 80 (P80) were prepared based on the DGMO/GMO-50 system, and their structure was correlated with the phase behavior of the corresponding bulk system. These NPs were characterized by dynamic light scattering (DLS), cryo-transmission electron microscopy (Cryo-TEM) and small angle X-ray scattering (SAXS) to determine their size, shape, and inner structure as a function of the DGMO/GMO-50 ratio. In addition, the effect of P80 as stabilizer was investigated. We found that the NPs have aqueous pores with diameters up to 13 nm, similar to the ones in the bulk phase. PMID:27482838

  10. Development of a correlation for aqueous-vapor phase mass transfer in porous media

    Science.gov (United States)

    Szatkowski, Andrew; Imhoff, Paul T.; Miller, Cass T.

    1995-03-01

    In many situations vapor-phase extraction procedures (e.g., soil venting, air sparging, and bioventing) may be suitable methods for remediating porous media contaminated by volatile organic compounds. This has led to increased study of operative processes in these systems, including aqueous-vapor phase mass transfer. Past work has shown the importance of the flow regime on this process, but a quantitative estimate of mass-transfer coefficients is lacking, especially for systems not confounded by uncertainties involving interfacial area between the phases. An experimental investigation was conducted to isolate the resistance to aqueous-vapor phase mass transfer at the phase boundary, using an ideal porous medium system. Mass-transfer coefficients were measured for toluene for a wide range of Reynolds numbers. An empirical model was fit to the data in dimensionless form. The mass-transfer model was coupled with an available interfacial area model, yielding a dimensionless expression for the mass-transfer rate coefficient. This expression was used to compare results from this work to three other experimental studies reported in the literature. These comparisons showed that for experiments where infiltrating water flowed uniformly within the porous medium, the predicted mass-transfer coefficients were within a factor of 5 of the measured coefficients. Mass transfer was significantly slower than the rate predicted, using the results from this work, in experiments where infiltrating water flowed nonuniformly.

  11. Experimental Study on Aqueous Phase Entrainment in a Mixer-settler with Double Stirring Mode

    Institute of Scientific and Technical Information of China (English)

    Wang Shuchan; Zhang Tingan; Zhao Qiuyue; Liu Yan; Wu Qiuyang

    2013-01-01

    The mixer-settler is a core device of solvent extraction for separating rare earth elements. There are some adverse effects like high rare earth accumulation and poor production efifciency during industrial production. Current researches usually focus on changing the structure of the mixer-settler without making a breakthrough towards gravity clariifcation. In this paper, in order to improve the efifciency of clariifcation, a mixer-settler with double stirring mode was designed and manufactured by adding a stirring device in the settler after reducing the volume of the settler. The innovation of this research involves adopting the ultraviolet-visible spectrophotometer to investigate the quantity of aqueous phase entrainment at the settler outlet in order to measure the clariifcation degree. Experimental results show that the clariifcation effect with stirring is better than that without stirring. The clariifcation effect is ameliorated as the stirring speed increases. Generally, the clariifcation effect shows a best condition when the offset distance is 12.5 cm, making the phase entrainment reduced to less than 0.1%. When the clearance over the tank bottom is 7 cm and 10 cm, respectively, the quantity of aqueous phase entrainment is better than the case with a clearance of 4 cm. The results show that the stirring paddle close to the mixed phase zone can better promote the two-phase separation.

  12. Low-temperature aqueous-phase reforming of ethanol on bimetallic PdZn catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Xiong, Haifeng; DelaRiva, Andrew; Wang, Yong; Dayte, Abhaya

    2015-01-01

    Bimetallic PdZn catalysts supported on carbon black (CB) and carbon nanotubes (CNTs) were found to be selective for CO-free H-2 production from ethanol at low temperature (250 degrees C). On Pd, the H-2 yield was low (similar to 0.3 mol H-2/mol ethanol reacted) and the CH4/CO2 ratio was high (similar to 1.7). Addition of Zn to Pd formed the intermetallic PdZn beta phase (atomic ratio of Zn to Pd is 1) with increased H-2 yield (similar to 1.9 mol H-2/mol ethanol reacted) and CH4/CO2 ratio of <1. The higher H-2 yield and low CH4 formation was related to the improved dehydrogenation activity of the L1(0) PdZn beta phase. The TOF increased with particle size and the CNTs provided the most active and selective catalysts, which may be ascribed to pore-confinement effects. Furthermore, no significant changes in either the supports or the PdZn beta particles was found after aqueous-phase reforming (APR) indicating that the metal nanoparticles and the carbon support are hydrothermally stable in the aqueous phase at elevated temperatures and pressures (>200 degrees C, 65 bar). No CO was detected for all the catalysts performed in aqueous-phase reaction, indicating that both monometallic Pd and bimetallic PdZn catalysts have high water-gas shift activity during APR. However, the yield of H-2 is considerably lower than the theoretical value of 6 H-2 per mole ethanol which is due to the presence of oxygenated products and methane on the PdZn catalysts.

  13. 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.

  14. Transport of intensity phase imaging using Bessel sources

    Science.gov (United States)

    Petruccelli, Jonathan C.; Chakraborty, Tonmoy

    2016-05-01

    Propagation-based phase contrast using the transport of intensity equation (TIE) allows rapid, deterministic phase retrieval from defocused images. For weakly attenuating objects, phase can be retrieved from a single image. However, the TIE suffers from significant low frequency artifacts due to enhancement of noise during phase retrieval. We demonstrate that by patterning the illumination source as approximately a modified Bessel function of the 2nd kind of zero order, quantitative phase can be imaged directly at the detector within a spatial frequency band. Outside of that band, Bessel sources still improve low frequency performance in phase retrieval.

  15. Distribution of selected halogenated organic compounds among suspended particulate, colloid, and aqueous phases in the Mississippi River and major tributaries

    Science.gov (United States)

    Rostad, C.E.; Daniel, S.R.

    2007-01-01

    Suspended particulate, colloid, and aqueous phases were separated and analyzed to determine spatial variation of specific organic compound transport associated with each phase in a dynamic river system. Sixteen sites along the Mississippi River and its major tributaries were sampled at low-flow conditions to maximize the possibility of equilibrium. Across the solubility range studied, the proportion transported by each phase depended on the compound solubility, with more water-soluble compounds (dacthal, trifluralin) transported predominantly in the aqueous phase and less-water soluble compounds (polychlorinated biphenyls, chlordane-related compounds) transported predominantly in the particulate and colloid phases. ?? 2007 Springer Science+Business Media, LLC.

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

    Science.gov (United States)

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

    2013-08-30

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

  17. Aqueous phase oxidation of sulphur dioxide by ozone in cloud droplets

    Science.gov (United States)

    Hoyle, C. R.; Fuchs, C.; Järvinen, E.; Saathoff, H.; Dias, A.; El Haddad, I.; Gysel, M.; Coburn, S. C.; Tröstl, J.; Bernhammer, A.-K.; Bianchi, F.; Breitenlechner, M.; Corbin, J. C.; Craven, J.; Donahue, N. M.; Duplissy, J.; Ehrhart, S.; Frege, C.; Gordon, H.; Höppel, N.; Heinritzi, M.; Kristensen, T. B.; Molteni, U.; Nichman, L.; Pinterich, T.; Prévôt, A. S. H.; Simon, M.; Slowik, J. G.; Steiner, G.; Tomé, A.; Vogel, A. L.; Volkamer, R.; Wagner, A. C.; Wagner, R.; Wexler, A. S.; Williamson, C.; Winkler, P. M.; Yan, C.; Amorim, A.; Dommen, J.; Curtius, J.; Gallagher, M. W.; Flagan, R. C.; Hansel, A.; Kirkby, J.; Kulmala, M.; Möhler, O.; Stratmann, F.; Worsnop, D. R.; Baltensperger, U.

    2016-02-01

    The growth of aerosol due to the aqueous phase oxidation of sulfur dioxide by ozone was measured in laboratory-generated clouds created in the Cosmics Leaving OUtdoor Droplets (CLOUD) chamber at the European Organization for Nuclear Research (CERN). Experiments were performed at 10 and -10 °C, on acidic (sulfuric acid) and on partially to fully neutralised (ammonium sulfate) seed aerosol. Clouds were generated by performing an adiabatic expansion - pressurising the chamber to 220 hPa above atmospheric pressure, and then rapidly releasing the excess pressure, resulting in a cooling, condensation of water on the aerosol and a cloud lifetime of approximately 6 min. A model was developed to compare the observed aerosol growth with that predicted using oxidation rate constants previously measured in bulk solutions. The model captured the measured aerosol growth very well for experiments performed at 10 and -10 °C, indicating that, in contrast to some previous studies, the oxidation rates of SO2 in a dispersed aqueous system can be well represented by using accepted rate constants, based on bulk measurements. To the best of our knowledge, these are the first laboratory-based measurements of aqueous phase oxidation in a dispersed, super-cooled population of droplets. The measurements are therefore important in confirming that the extrapolation of currently accepted reaction rate constants to temperatures below 0 °C is correct.

  18. 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.

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

    International Nuclear Information System (INIS)

    This study developed a headspace liquid-phase microextraction (LPME) method by using a single aqueous drop in combination with high performance liquid chromatography (HPLC)-UV detection for the determination of methamphetamine (MAP) and amphetamine (AP) in urine samples. The analytes, volatile and basic, were released from sample matrix into the headspace first, and then protonated and dissolved in an aqueous H3PO4 drop hanging in the headspace by a HPLC syringe. After extraction, this drop was directly injected into HPLC. Parameters affecting extraction efficiency were investigated and optimized. This method showed good linearity in the investigated concentration range of 1.0-1500 μg L-1, repeatability of the extraction (R.S.D. -1 for both analytes). Enrichment factors of about 400-fold and 220-fold were achieved for MAP and AP, respectively, at optimum conditions. The feasibility of the method was demonstrated by analyzing human urine samples

  20. Stability of clavulanic acid in PEG/citrate and liquid–liquid extraction in aqueous two-phase system

    OpenAIRE

    Carneiro-da-Cunha, M. N.; Souza, K. P. S.; Mota, A; J.A. Teixeira; Porto, C S; Porto, Tatiana Souza; Porto, Ana L. F.

    2014-01-01

    β-Lactamases are enzymes responsible for the hydrolysis of β-lactam antibiotics, being produced by several pathogenic bacteria. Clavulanic acid is a commercially and clinically important β-lactamase inhibitor, its extraction being possible by the application of aqueous two-phase system. In this study, clavulanic acid stability was investigated at different molar mass PEG (400, 1 000 and 20 000 g mol−1) and at different citrate concentrations (5 and 20%) PEG/citrate aqueous-two phase systems (...

  1. 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 ...

  2. The Effect of pH Difference Between Two Phases on the Partition of Lysozyme in Aqueous Two-Phase System

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    In the investigation of effect of KSCN on the partitioning of lysozyme in PEG2000/ammonium sulfate aqueous two-phase system, it was found that the KSCN could alter the pH difference between the two phases, and thus affect the partition of lysozyme. The relationship between partition coefficients of lysozyme and pH differences between two phases was discussed.

  3. Enhancement of a novel extracellular uricase production by media optimization and partial purification by aqueous three-phase system.

    Science.gov (United States)

    Ram, Senthoor K; Raval, Keyur; JagadeeshBabu, P E

    2015-01-01

    Uricase (urate: oxygen oxidoreductase, EC 1.7.3.3), an enzyme belonging to the class of oxidoreductases, catalyzes the enzymatic oxidation of uric acid to allantoin and finds a wide variety of application as therapeutic and clinical reagent. In this study, uricase production ability of the bacterial strains isolated from deep litter poultry soil is investigated. The strain with maximum extracellular uricase production capability was identified as Xanthomonas fuscans subsp. aurantifolii based on 16S rRNA sequencing. Effect of various carbon and nitrogen sources on uricase productivity was investigated. The uricase production for this strain was optimized using statistically based experimental designs and resulted in uricase activity of 306 U/L, which is 2 times higher than initial uricase activity. Two-step purification, such as ammonium sulfate precipitation and aqueous two-phase system, was carried out and a twofold increase in yield and specific activity was observed.

  4. Separation of synchronous sources through phase locked matrix factorization.

    Science.gov (United States)

    Almeida, Miguel S B; Vigário, Ricardo; Bioucas-Dias, José

    2014-10-01

    In this paper, we study the separation of synchronous sources (SSS) problem, which deals with the separation of sources whose phases are synchronous. This problem cannot be addressed through independent component analysis methods because synchronous sources are statistically dependent. We present a two-step algorithm, called phase locked matrix factorization (PLMF), to perform SSS. We also show that SSS is identifiable under some assumptions and that any global minimum of PLMFs cost function is a desirable solution for SSS. We extensively study the algorithm on simulated data and conclude that it can perform SSS with various numbers of sources and sensors and with various phase lags between the sources, both in the ideal (i.e., perfectly synchronous and nonnoisy) case, and with various levels of additive noise in the observed signals and of phase jitter in the sources. PMID:25291741

  5. 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.

  6. 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

  7. 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.

  8. 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.

  9. Formation of aqueous-phase α-hydroxyhydroperoxides (α-HHP: potential atmospheric impacts

    Directory of Open Access Journals (Sweden)

    R. Zhao

    2013-06-01

    Full Text Available The focus of this work is on quantifying the degree of the aqueous-phase formation of α-hydroxyhydroperoxides (α-HHPs via reversible nucleophilic addition of H2O2 to aldehydes. Formation of this class of highly oxygenated organic hydroperoxides represents a poorly characterized aqueous-phase processing pathway that may lead to enhanced SOA formation and aerosol toxicity. Specifically, the equilibrium constants of α-HHP formation have been determined using proton nuclear-magnetic-resonance (1H NMR spectroscopy and proton-transfer-reaction mass spectrometry (PTR-MS. Significant α-HHP formation was observed from formaldehyde, acetaldehyde, propionaldehyde, glycolaldehyde, glyoxylic acid, and methylglyoxal, but not from methacrolein and ketones. Low temperatures enhanced the formation of α-HHPs but slowed their formation rates. High inorganic salt concentrations shifted the equilibria toward the hydrated form of the aldehydes and slightly suppressed α-HHP formation. Using the experimental equilibrium constants, we predict the equilibrium concentration of α-HHPs to be in the μM level in cloud water, but it may also be present in the mM level in aerosol liquid water (ALW, where the concentrations of H2O2 and aldehydes can be high. Formation of α-HHPs in ALW may significantly affect the effective Henry's law constants of H2O2 and aldehydes but may not affect their gas-phase levels. The photochemistry and reactivity of this class of atmospheric species have not been studied.

  10. Formation of aqueous-phase α-hydroxyhydroperoxides (α-HHP): potential atmospheric impacts

    Science.gov (United States)

    Zhao, R.; Lee, A. K. Y.; Soong, R.; Simpson, A. J.; Abbatt, J. P. D.

    2013-06-01

    The focus of this work is on quantifying the degree of the aqueous-phase formation of α-hydroxyhydroperoxides (α-HHPs) via reversible nucleophilic addition of H2O2 to aldehydes. Formation of this class of highly oxygenated organic hydroperoxides represents a poorly characterized aqueous-phase processing pathway that may lead to enhanced SOA formation and aerosol toxicity. Specifically, the equilibrium constants of α-HHP formation have been determined using proton nuclear-magnetic-resonance (1H NMR) spectroscopy and proton-transfer-reaction mass spectrometry (PTR-MS). Significant α-HHP formation was observed from formaldehyde, acetaldehyde, propionaldehyde, glycolaldehyde, glyoxylic acid, and methylglyoxal, but not from methacrolein and ketones. Low temperatures enhanced the formation of α-HHPs but slowed their formation rates. High inorganic salt concentrations shifted the equilibria toward the hydrated form of the aldehydes and slightly suppressed α-HHP formation. Using the experimental equilibrium constants, we predict the equilibrium concentration of α-HHPs to be in the μM level in cloud water, but it may also be present in the mM level in aerosol liquid water (ALW), where the concentrations of H2O2 and aldehydes can be high. Formation of α-HHPs in ALW may significantly affect the effective Henry's law constants of H2O2 and aldehydes but may not affect their gas-phase levels. The photochemistry and reactivity of this class of atmospheric species have not been studied.

  11. The phase transport and reactions of γ-irradiated aqueous-ionic liquids

    International Nuclear Information System (INIS)

    A novel technology based on the transfer of chemical species across water/ionic liquid interfaces via specific complexation reactions is currently being considered for the separation and sequestration of metal ion contaminants from radioactive waste effluents in the nuclear fuel cycle. An ideal solvent for these applications should have a high intrinsic selectivity for a targeted metal or group of metals (e.g., trans-Pu actinides, lanthanides, or other fission products), an efficient switching mechanism (between complexation and decomplexation), and a high immiscibility with aqueous solutions. These characteristics must be maintained in the chemical, radiation, and mass transport environments present during the separation process. Ionic liquids (ILs) have an almost negligible vapour pressure and high thermal stability. Their ability to dissolve a wide range of substrate molecules and potential to be highly resilient in radiation fields make ILs particularly promising media. The separation efficiency of the biphasic system will depend on many parameters, including the aqueous oxidation state of the targeted metal ion, and the thermodynamics and kinetics of interfacial transport and metal-ligand complex formation at the water/IL interface or in the IL phase. The most uncertain and unstudied area for these applications is the effect of ionizing radiation on the stability and separation efficiency of the biphasic system. The present study investigates the effect of γ-radiation on gas/IL and water/IL interfacial stability and mass transfer with trihexyltetradecylphosphonium bis(trifluoromethyl-sulfonyl)imide, a phosphonium-based IL. The IL, in contact with either gas or water, was irradiated at a dose rate of 6.4 kGy·h-1. Gas-phase samples were analyzed by gas chromatography-mass spectrometry (GC-MS) and the changes in the IL and aqueous phases were monitored by conductivity measurements and Raman spectroscopy. In this paper we discuss these observations and their

  12. Extraction of Phenylalanine Phase Systems Containing Enantiomers by Aqueous Two Combinatorial Chiral Selector

    Institute of Scientific and Technical Information of China (English)

    陈晓青; 刘莉; 焦飞鹏; 王珍

    2012-01-01

    In order to obtain a better enantioselectivity of phenylalanine enantiomers and establish the optimal chiral ex- traction conditions, the distribution behavior was investigated in aqueous two-phase systems which were composed of polyethylene glycol and ammonium sulfate containing combinatorial chiral selector: β-cyclodextrin and HP-β-cyclodextrin. The influence of the molar concentration ratio of combinatorial chiral selectors, the total molar concentration of combinatorial chiral selectors, pH value, buffer type and its concentration were thoroughly studied, respectively. The results show that the enantioselectivity reaches 1.53 under the optimal chiral extraction conditions This extraction is a potential economical and effective way for chiral resolution.

  13. Preparation and adsorption performance of a novel bipolar PS-EDTA resin in aqueous phase

    International Nuclear Information System (INIS)

    A novel chelating resin containing many amino and carboxyl functional groups, PS-EDTA resin, was prepared from chloromethylated polystyrene bead by reacting with ethylenediamine and chloroacetate in aqueous phase in sequence. The structure of PS-EDTA resin was characterized by means of infrared spectroscopy, scanning electron microscopy, surface area analysis and thermogravimetry. Adsorption behavior of the resin for Ag (I) ions in aqueous solutions was investigated by batch experiments. The results indicated that the adsorption removal of PS-EDTA resin for Ag (I) could achieve more than 99.9% at pH values of 5.0 with an initial Ag (I) concentration of 60.0 mg/L within 2 h. The maximum removal capacity of PS-EDTA toward Ag (I) was found to be almost 3314.97 mg/g at 25 deg. C. In addition, adsorption kinetic data were described by pseudo-second-order equation and the equilibrium data fitted very well with the Freundlich model. It was found that the PS-EDTA resin had excellent adsorption properties for Ag (I), so it should be a promising composite adsorbent with application in the recovery of Ag (I) ions from aqueous environment.

  14. Three phase voltage source converter current analysis

    International Nuclear Information System (INIS)

    The proposed rectifier system consists of a three-phase diode bridge circuit as a main power circuit, A C reactors, and an additional circuit, which serves as an active filter with low switching frequencies and forced-commutation circuit for the diodes. These papers describe the operation principle, analysis of the waveforms of input voltage and current, the calculated of A C input current, multiple phase-shifted systems, and the experimental result. Avery conventional method was employed to analyze the input current equation; in that, the ripple output was neglected. The theory developed in this paper was verified twice; by calculation result and experiments. The calculated A C input the simple program using the algorithm of current equations calculated current waveforms presented in this paper. A switching circuit has been added to the diode rectifier, serving as an active filter and a forced-commutation circuit for diodes systems

  15. Phased-array sources based on nonlinear metamaterial nanocavities.

    Science.gov (United States)

    Wolf, Omri; Campione, Salvatore; Benz, Alexander; Ravikumar, Arvind P; Liu, Sheng; Luk, Ting S; Kadlec, Emil A; Shaner, Eric A; Klem, John F; Sinclair, Michael B; Brener, Igal

    2015-07-01

    Coherent superposition of light from subwavelength sources is an attractive prospect for the manipulation of the direction, shape and polarization of optical beams. This phenomenon constitutes the basis of phased arrays, commonly used at microwave and radio frequencies. Here we propose a new concept for phased-array sources at infrared frequencies based on metamaterial nanocavities coupled to a highly nonlinear semiconductor heterostructure. Optical pumping of the nanocavity induces a localized, phase-locked, nonlinear resonant polarization that acts as a source feed for a higher-order resonance of the nanocavity. Varying the nanocavity design enables the production of beams with arbitrary shape and polarization. As an example, we demonstrate two second harmonic phased-array sources that perform two optical functions at the second harmonic wavelength (∼5 μm): a beam splitter and a polarizing beam splitter. Proper design of the nanocavity and nonlinear heterostructure will enable such phased arrays to span most of the infrared spectrum.

  16. 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.

  17. Using design of experiments to optimize derivatization with methyl chloroformate for quantitative analysis of aqueous phase from hydrothermal liquefaction of biomass

    DEFF Research Database (Denmark)

    Madsen, René Bjerregaard; Jensen, Mads Mørk; Mørup, Anders;

    2016-01-01

    Hydrothermal liquefaction is a promising technique for the production of bio-oil. The process produces an oil phase, a gas phase, a solid residue, and an aqueous phase. Gas chromatography coupled with mass spectrometry is used to analyze the complex aqueous phase. Especially small organic acids a...

  18. Carbon Mineralization by Aqueous Precipitation for Beneficial Use of CO2 from Flue Gas. Phase I. Final Topical Report

    International Nuclear Information System (INIS)

    Calera's innovative Mineralization via Aqueous Precipitation (MAP) technology for the capture and conversion of CO2 to useful materials for use in the built environment was further developed and proven in the Phase 1 Department of Energy Grant. The process was scaled to 300 gallon batch reactors and subsequently to Pilot Plant scale for the continuous production of product with the production of reactive calcium carbonate material that was evaluated as a supplementary cementitious material (SCM). The Calera SCM(trademark) was evaluated as a 20% replacement for ordinary portland cement and demonstrated to meet the industry specification ASTM 1157 which is a standard performance specification for hydraulic cement. The performance of the 20% replacement material was comparable to the 100% ordinary portland cement control in terms of compressive strength and workability as measured by a variety of ASTM standard tests. In addition to the performance metrics, detailed characterization of the Calera SCM was performed using advanced analytical techniques to better understand the material interaction with the phases of ordinary portland cement. X-ray synchrotron diffraction studies at the Advanced Photon Source in Argonne National Lab confirmed the presence of an amorphous phase(s) in addition to the crystalline calcium carbonate phases in the reactive carbonate material. The presence of carboaluminate phases as a result of the interaction of the reactive carbonate materials with ordinary portland cement was also confirmed. A Life Cycle Assessment was completed for several cases based on different Calera process configurations and compared against the life cycle of ordinary portland cement. In addition to the materials development efforts, the Calera technology for the production of product using an innovative building materials demonstration plant was developed beyond conceptual engineering to a detailed design with a construction schedule and cost estimate.

  19. Interfacial tension between a complex coacervate phase and its coexisting aqueous phase

    NARCIS (Netherlands)

    Spruijt, E.; Sprakel, J.H.B.; Cohen Stuart, M.A.; Gucht, van der J.

    2010-01-01

    Complex coacervation is the associative phase separation in a solution of positively and negatively charged macroions. Despite the widespread use of coacervation in e.g. micellar assemblies (complex coacervate core micelles), drug carriers and thin films, there is virtually no experimental data on t

  20. Quantification of colloidal and aqueous element transfer in soils: The dual-phase mass balance model

    Science.gov (United States)

    Bern, Carleton R.; Thompson, Aaron; Chadwick, Oliver A.

    2015-01-01

    Mass balance models have become standard tools for characterizing element gains and losses and volumetric change during weathering and soil development. However, they rely on the assumption of complete immobility for an index element such as Ti or Zr. Here we describe a dual-phase mass balance model that eliminates the need for an assumption of immobility and in the process quantifies the contribution of aqueous versus colloidal element transfer. In the model, the high field strength elements Ti and Zr are assumed to be mobile only as suspended solids (colloids) and can therefore be used to distinguish elemental redistribution via colloids from redistribution via dissolved aqueous solutes. Calculations are based upon element concentrations in soil, parent material, and colloids dispersed from soil in the laboratory. We illustrate the utility of this model using a catena in South Africa. Traditional mass balance models systematically distort elemental gains and losses and changes in soil volume in this catena due to significant redistribution of Zr-bearing colloids. Applying the dual-phase model accounts for this colloidal redistribution and we find that the process accounts for a substantial portion of the major element (e.g., Al, Fe and Si) loss from eluvial soil. In addition, we find that in illuvial soils along this catena, gains of colloidal material significantly offset aqueous elemental loss. In other settings, processes such as accumulation of exogenous dust can mimic the geochemical effects of colloid redistribution and we suggest strategies for distinguishing between the two. The movement of clays and colloidal material is a major process in weathering and pedogenesis; the mass balance model presented here is a tool for quantifying effects of that process over time scales of soil development.

  1. Anti-Adhesive Behaviors between Solid Hydrate and Liquid Aqueous Phase Induced by Hydrophobic Silica Nanoparticles.

    Science.gov (United States)

    Min, Juwon; Baek, Seungjun; Somasundaran, P; Lee, Jae W

    2016-09-20

    This study introduces an "anti-adhesive force" at the interface of solid hydrate and liquid solution phases. The force was induced by the presence of hydrophobic silica nanoparticles or one of the common anti-agglomerants (AAs), sorbitan monolaurate (Span 20), at the interface. The anti-adhesive force, which is defined as the maximum pushing force that does not induce the formation of a capillary bridge between the cyclopentane (CP) hydrate particle and the aqueous solution, was measured using a microbalance. Both hydrophobic silica nanoparticles and Span 20 can inhibit adhesion between the CP hydrate probe and the aqueous phase because silica nanoparticles have an aggregative property at the interface, and Span 20 enables the hydrate surface to be wetted with oil. Adding water-soluble sodium dodecyl sulfate (SDS) to the nanoparticle system cannot affect the aggregative property or the distribution of silica nanoparticles at the interface and, thus, cannot change the anti-adhesive effect. However, the combined system of Span 20 and SDS dramatically reduces the interfacial tension: emulsion drops were formed at the interface without any energy input and were adsorbed on the CP hydrate surface, which can cause the growth of hydrate particles. Silica nanoparticles have a good anti-adhesive performance with a relatively smaller dosage and are less influenced by the presence of molecular surfactants; consequently, these nanoparticles may have a good potential for hydrate inhibition as AAs. PMID:27564571

  2. Aqueous phase adsorption of different sized molecules on activated carbon fibers: Effect of textural properties.

    Science.gov (United States)

    Prajapati, Yogendra N; Bhaduri, Bhaskar; Joshi, Harish C; Srivastava, Anurag; Verma, Nishith

    2016-07-01

    The effect that the textural properties of rayon-based activated carbon fibers (ACFs), such as the BET surface area and pore size distribution (PSD), have on the adsorption of differently sized molecules, namely, brilliant yellow (BY), methyl orange (MO) and phenol (PH), was investigated in the aqueous phase. ACF samples with different BET areas and PSDs were produced by steam-activating carbonized fibers for different activation times (0.25, 0.5, and 1 h). The samples activated for 0.25 h were predominantly microporous, whereas those activated for relatively longer times contained hierarchical micro-mesopores. The adsorption capacities of the ACFs for the adsorbate increased with increasing BET surface area and pore volume, and ranged from 51 to 1306 mg/g depending on the textural properties of the ACFs and adsorbate size. The adsorption capacities of the hierarchical ACF samples followed the order BY > MO > PH. Interestingly, the number of molecules adsorbed by the ACFs followed the reverse order: PH > MO > BY. This anomaly was attributed to the increasing molecular weight of the PH, MO and BY molecules. The equilibrium adsorption data were described using the Langmuir isotherm. This study shows that suitable textural modifications to ACFs are required for the efficient aqueous phase removal of an adsorbate. PMID:27107386

  3. THERMAL PERFORMANCE OF A TWO PHASE CLOSED THERMOSYPHON USING AQUEOUS SOLUTION

    Directory of Open Access Journals (Sweden)

    M. Karthikeyan

    2010-05-01

    Full Text Available The thermal performance of an inclined two phase closed thermosyphon with different working fluid has been investigated experimentally in this paper. Distilled water and an aqueous solution that has a positive gradient of surface tension with temperature are used as the working fluid. A copper thermosyphon with a length of 1000 mm long, an inner diameter of 17 mm and an outer diameter of 19 mm was mployed. Each thermosyphon was charged with 60% of the working fluid and was tested with an evaporator length of 400 mm and condenser length of 450 mm. The thermosyphon was tested for various inclinations of 45○, 60○ and 90○ to the horizontal. Flow rate of 0.08Kg/min, 0.1 Kg/min and 0.12 Kg/min and heat input of 40 W, 60 W and 80 W were taken as input parameters. The thermal performance of aqueous solution charged two phase closed thermosyphon was out performed the distilled water in both heat transfer and temperature distribution.

  4. Herschel-ATLAS: Planck sources in the Phase 1 fields

    OpenAIRE

    Herranz, D.; González-Nuevo, J.; Clements, D. L.; López-Caniego, M.; Lapi, A.; Danese, L.; Fu, Hai; Baes, M.; Carrera, Francisco J.; Eales, S.; Ivison, R. J.; Jarvis, Matt J.; Lagache, G.; Massardi, Marcella; Negrello, Mattia

    2012-01-01

    We present the results of a cross-correlation of the Planck Early Release Compact Source catalogue (ERCSC) with the catalogue of Herschel-ATLAS sources detected in the phase 1 fields, covering 134.55 deg2. There are 28ERCSC sources detected by Planck at 857GHz in this area. Asmany as16 of them are probably high Galactic latitude cirrus; 10additional sources can be clearly identified as bright, low-z galaxies; one further source is resolved by Herschel as two relatively bright sources; and the...

  5. Measurement and Correlation of Equilibrium Data for Aqueous Two-phase System Ethanol+Water+K2HPO4

    Institute of Scientific and Technical Information of China (English)

    LIN Jin-qing; TAN Ping-hua; JIN Chun-ying; LI Ming-chun

    2004-01-01

    The isothermal solubility data of aqueous two-phase system ethanol+water+K2HPO4 were determined with the turbidity titration method at 303.2 K. The binodal curves were described by using the Mistry equation very well. An experimental procedure for measuring the liquid-liquid equilibrium data of the aqueous two-phase system was proposed, in which the concentrations of the coexisting phases were determined with the corresponding densities of the solution. The tie lines were satisfactorily described by using the Othmer Tobias and Bancroft equations.

  6. Salt effect on the (polyethylene glycol 8000 + sodium sulfate) aqueous two-phase system: Relative hydrophobicity of the equilibrium phases

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Luisa A., E-mail: laferreira@deb.uminho.pt [IBB - Institute for Biotechnology and Bioengineering, Centre for Biological Engineering, Universidade do Minho, Campus de Gualtar, 4710-057 Braga (Portugal); Teixeira, Jose A. [IBB - Institute for Biotechnology and Bioengineering, Centre for Biological Engineering, Universidade do Minho, Campus de Gualtar, 4710-057 Braga (Portugal)

    2011-08-15

    Highlights: > Gibbs free energy of transfer of a methylene group on PEG 8000 - Na{sub 2}SO{sub 4} ATPS. > Influence of salt additive on the hydrophobic character of the coexisting phases. > Partitioning behavior of a series of five sodium salts of DNP-amino acids. > A relationship between {Delta}G(CH{sub 2}), TLL and I of the salt additive was established. - Abstract: The relative hydrophobicity of the phases of several {l_brace}polyethylene glycol (PEG) 8000 + sodium sulfate (Na{sub 2}SO{sub 4}){r_brace} aqueous two-phase systems (ATPSs), all containing 0.01 mol . L{sup -1} sodium phosphate buffer (NaPB, pH 7.4) and increasing concentration of a salt additive, NaCl or KCl, up to 1.0 mol . L{sup -1}, was measured by the free energy of transfer of a methylene group between the phases, {Delta}G(CH{sub 2}). The {Delta}G(CH{sub 2}) of the systems was determined by partitioning of a homologous series of five sodium salts of dinitrophenylated (DNP) - amino acids with aliphatic side chains in three different tie-lines of each biphasic system. The relative hydrophobicity of the phases ranged from -0.125 to -0.183 kcal . mol{sup -1}, being the NaCl salt the one to provide the more effective changes. The results show that, within each system, there is a linear relationship between the {Delta}G(CH{sub 2}) and the tie-line length (TLL), and biphasic systems with high salt additive concentration present the most negative {Delta}G(CH{sub 2}) values. Therefore, the feasibility of establishing a relationship between the relative hydrophobicity of the phases in a given TLL and the ionic strength of the salt additive was investigated and a satisfactory correlation was found for each salt.

  7. Improving the treatment of non-aqueous phase TCE in low permeability zones with permanganate

    Energy Technology Data Exchange (ETDEWEB)

    Chokejaroenrat, Chanat, E-mail: chanat@sut.ac.th [Department of Civil Engineering, University of Nebraska, Lincoln, NE 68588-0531 (United States); School of Environmental Engineering, Institute of Engineering, Suranaree University of Technology, Nakhon Ratchasima 30000 (Thailand); Comfort, Steve, E-mail: scomfort1@unl.edu [School of Natural Resources, University of Nebraska, Lincoln, NE 68583-0915 (United States); Sakulthaew, Chainarong, E-mail: cvtcns@ku.ac.th [School of Natural Resources, University of Nebraska, Lincoln, NE 68583-0915 (United States); Department of Veterinary Technology, Kasetsart University, Bangkok 10900 (Thailand); Dvorak, Bruce, E-mail: bdvorak1@unl.edu [Department of Civil Engineering, University of Nebraska, Lincoln, NE 68588-0531 (United States)

    2014-03-01

    Graphical abstract: - Highlights: • Transport experiments used transmissive and low permeability zones (LPZs). • {sup 14}C-labeled TCE was used to quantify oxidation of DNAPL in LPZs by permanganate. • Stabilization aids prevented MnO{sub 2} rind formation. • DNAPL oxidation improved when xanthan and stabilization aids were used. - Abstract: Treating dense non-aqueous phase liquids (DNAPLs) embedded in low permeability zones (LPZs) is a particularly challenging issue for injection-based remedial treatments. Our objective was to improve the sweeping efficiency of permanganate (MnO{sub 4}{sup −}) into LPZs to treat high concentrations of TCE. This was accomplished by conducting transport experiments that quantified the penetration of various permanganate flooding solutions into a LPZ that was spiked with non-aqueous phase {sup 14}C-TCE. The treatments we evaluated included permanganate paired with: (i) a shear-thinning polymer (xanthan); (ii) stabilization aids that minimized MnO{sub 2} rind formation and (iii) a phase-transfer catalyst. In addition, we quantified the ability of these flooding solutions to improve TCE destruction under batch conditions by developing miniature LPZ cylinders that were spiked with {sup 14}C-TCE. Transport experiments showed that MnO{sub 4}{sup −} alone was inefficient in penetrating the LPZ and reacting with non-aqueous phase TCE, due to a distinct and large MnO{sub 2} rind that inhibited the TCE from further oxidant contact. By including xanthan with MnO{sub 4}{sup −}, the sweeping efficiency increased (90%) but rind formation was still evident. By including the stabilization aid, sodium hexametaphosphate (SHMP) with xanthan, permanganate penetrated 100% of the LPZ, no rind was observed, and the percentage of TCE oxidized increased. Batch experiments using LPZ cylinders allowed longer contact times between the flooding solutions and the DNAPL and results showed that SHMP + MnO{sub 4}{sup −} improved TCE destruction by

  8. Improving the treatment of non-aqueous phase TCE in low permeability zones with permanganate

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Transport experiments used transmissive and low permeability zones (LPZs). • 14C-labeled TCE was used to quantify oxidation of DNAPL in LPZs by permanganate. • Stabilization aids prevented MnO2 rind formation. • DNAPL oxidation improved when xanthan and stabilization aids were used. - Abstract: Treating dense non-aqueous phase liquids (DNAPLs) embedded in low permeability zones (LPZs) is a particularly challenging issue for injection-based remedial treatments. Our objective was to improve the sweeping efficiency of permanganate (MnO4−) into LPZs to treat high concentrations of TCE. This was accomplished by conducting transport experiments that quantified the penetration of various permanganate flooding solutions into a LPZ that was spiked with non-aqueous phase 14C-TCE. The treatments we evaluated included permanganate paired with: (i) a shear-thinning polymer (xanthan); (ii) stabilization aids that minimized MnO2 rind formation and (iii) a phase-transfer catalyst. In addition, we quantified the ability of these flooding solutions to improve TCE destruction under batch conditions by developing miniature LPZ cylinders that were spiked with 14C-TCE. Transport experiments showed that MnO4− alone was inefficient in penetrating the LPZ and reacting with non-aqueous phase TCE, due to a distinct and large MnO2 rind that inhibited the TCE from further oxidant contact. By including xanthan with MnO4−, the sweeping efficiency increased (90%) but rind formation was still evident. By including the stabilization aid, sodium hexametaphosphate (SHMP) with xanthan, permanganate penetrated 100% of the LPZ, no rind was observed, and the percentage of TCE oxidized increased. Batch experiments using LPZ cylinders allowed longer contact times between the flooding solutions and the DNAPL and results showed that SHMP + MnO4− improved TCE destruction by ∼16% over MnO4− alone (56.5% vs. 40.1%). These results support combining

  9. Herschel-ATLAS: Planck sources in the Phase 1 fields

    CERN Document Server

    Herranz, D; Clements, D L; Clemens, M; De Zotti, G; López-Caniego, M; Lapi, A; Rodighiero, G; Danese, L; Fu, H; Cooray, A; Baes, M; Bendo, G J; Bonavera, L; Carrera, F J; Dole, H; Eales, S; Ivison, R J; Jarvis, M; Lagache, G; Massardi, M; Michalowski, M J; Negrello, M; Rigby, E; Scott, D; Valiante, E; Valtchanov, I; Van der Werf, P; Auld, R; Buttiglione, S; Dariush, A; Dunne, L; Hopwood, R; Hoyos, C; Ibar, E; Maddox, S

    2012-01-01

    We present the results of a cross-correlation of the Planck Early Release Compact Source Catalog (ERCSC) with the catalog of Herschel-ATLAS sources detected in the Phase 1 fields, covering 134.55 deg2. There are 28 ERCSC sources detected by Planck at 857 GHz in this area. As many as 16 of them are probably high Galactic latitude cirrus; 10 additional sources can be clearly identified as bright, low-z galaxies; one further source is resolved by Herschel as two relatively bright sources; and the last is resolved into an unusual condensation of low-flux, probably high-redshift point sources, around a strongly lensed Herschel-ATLAS source at z = 3.26. Our results demonstrate that the higher sensitivity and higher angular resolution H-ATLAS maps provide essential information for the interpretation of candidate sources extracted from Planck sub-mm maps.

  10. Molecular transformations of phenolic SOA during photochemical aging in the aqueous phase: competition among oligomerization, functionalization, and fragmentation

    Science.gov (United States)

    Yu, Lu; Smith, Jeremy; Laskin, Alexander; George, Katheryn M.; Anastasio, Cort; Laskin, Julia; Dillner, Ann M.; Zhang, Qi

    2016-04-01

    Organic aerosol is formed and transformed in atmospheric aqueous phases (e.g., cloud and fog droplets and deliquesced airborne particles containing small amounts of water) through a multitude of chemical reactions. Understanding these reactions is important for a predictive understanding of atmospheric aging of aerosols and their impacts on climate, air quality, and human health. In this study, we investigate the chemical evolution of aqueous secondary organic aerosol (aqSOA) formed during reactions of phenolic compounds with two oxidants - the triplet excited state of an aromatic carbonyl (3C∗) and hydroxyl radical (•OH). Changes in the molecular composition of aqSOA as a function of aging time are characterized using an offline nanospray desorption electrospray ionization mass spectrometer (nano-DESI MS) whereas the real-time evolution of SOA mass, elemental ratios, and average carbon oxidation state (OSC) are monitored using an online aerosol mass spectrometer (AMS). Our results indicate that oligomerization is an important aqueous reaction pathway for phenols, especially during the initial stage of photooxidation equivalent to ˜ 2 h irradiation under midday winter solstice sunlight in Northern California. At later reaction times functionalization (i.e., adding polar oxygenated functional groups to the molecule) and fragmentation (i.e., breaking of covalent bonds) become more important processes, forming a large variety of functionalized aromatic and open-ring products with higher OSC values. Fragmentation reactions eventually dominate the photochemical evolution of phenolic aqSOA, forming a large number of highly oxygenated ring-opening molecules with carbon numbers (nC) below 6. The average nC of phenolic aqSOA decreases while average OSC increases over the course of photochemical aging. In addition, the saturation vapor pressures (C∗) of dozens of the most abundant phenolic aqSOA molecules are estimated. A wide range of C∗ values is observed, varying

  11. Molecular transformations of phenolic SOA during photochemical aging in the aqueous phase: competition among oligomerization, functionalization, and fragmentation

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Lu; Smith, Jeremy; Laskin, Alexander; George, Kathryn; Anastasio, Cort N.; Laskin, Julia; Dillner, Ann M.; Zhang, Qi

    2016-04-13

    Organic aerosol is formed and transformed in atmospheric aqueous phases (e.g., cloud and fog droplets and aerosol particles containing small amounts of water) through a multitude of chemical reactions. Understanding these reactions is important for a predictive understanding of atmospheric aging of aerosol particles and their impacts on climate, air quality, and human health. In this study, we investigate the chemical evolution of aqueous secondary organic aerosol (aqSOA) formed during reactions of phenolic compounds with two oxidants – the triplet excited state of an aromatic carbonyl (3C*) and hydroxyl radical (•OH). Changes in the molecular composition of aqSOA as a function of aging time are characterized using an offline nanospray desorption electrospray ionization mass spectrometer (nano-DESI MS) whereas the real-time evolution of SOA mass, elemental ratios, and average carbon oxidation state (OSC) are monitored using an online aerosol mass spectrometer (AMS). Our results indicate that oligomerization is an important aqueous reaction pathway for phenols, especially during the initial stage of photooxidation equivalent to ~ 2 hours irradiation under midday, winter solstice sunlight in northern California. At later reaction times functionalization (i.e., adding polar oxygenated functional groups to the molecule) and fragmentation (i.e., breaking of covalent bonds) become more important processes, forming a large variety of functionalized aromatic and open-ring products with higher OSC values. Fragmentation reactions eventually dominate the photochemical evolution of phenolic aqSOA, forming a large number of highly oxygenated open-ring molecules with carbon numbers (nC) below 6. The average nC of phenolic aqSOA decreases while average OSC increases over the course of photochemical aging. In addition, the saturation vapor pressures (C*) of dozens of the most abundant phenolic aqSOA molecules are estimated. A wide range of C* values is observed, varying from

  12. Molecular transformations of phenolic SOA during photochemical aging in the aqueous phase: competition among oligomerization, functionalization, and fragmentation

    Directory of Open Access Journals (Sweden)

    L. Yu

    2015-10-01

    Full Text Available Organic aerosol is formed and transformed in atmospheric aqueous phases (e.g., cloud and fog droplets and deliquesced airborne particles containing small amounts of water through a multitude of chemical reactions. Understanding these reactions is important for a predictive understanding of atmospheric aging of aerosols and their impacts on climate, air quality, and human health. In this study, we investigate the chemical evolution of aqueous secondary organic aerosol (aqSOA formed during reactions of phenolic compounds with two oxidants – the triplet excited state of an aromatic carbonyl (3C* and hydroxyl radical (•OH. Changes in the molecular composition of aqSOA as a function of aging time are characterized using an offline nanospray desorption electrospray ionization mass spectrometer (nano-DESI MS whereas the real-time evolution of SOA mass, elemental ratios, and average carbon oxidation state (OSC are monitored using an online aerosol mass spectrometer (AMS. Our results indicate that oligomerization is an important aqueous reaction pathway for phenols, especially during the initial stage of photooxidation equivalent to ∼ 2 h irradiation under midday, winter solstice sunlight in northern California. At later reaction times functionalization (i.e., adding polar oxygenated functional groups to the molecule and fragmentation (i.e., breaking of covalent bonds become more important processes, forming a large variety of functionalized aromatic and open-ring products with higher OSC values. Fragmentation reactions eventually dominate the photochemical evolution of phenolic aqSOA, forming a large number of highly oxygenated open-ring molecules with carbon numbers (nC below 6. The average nC of phenolic aqSOA decreases while average OSC increases over the course of photochemical aging. In addition, the saturation vapor pressures C* of dozens of the most abundant phenolic aqSOA molecules are estimated. A wide range of C* values is

  13. 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.

  14. 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

  15. Influence of aqueous phase on electrochemical biocorrosion tests in diesel/water systems

    Energy Technology Data Exchange (ETDEWEB)

    Bento, F.M. [Dept. of Soils, Faculty of Agronomy, UFRGS, 7712 Bento Goncalves Avenue, CEP: 91540-001, POA, RS (Brazil); Englert, G.E.; Muller, I.L. [Dept. of Metallurgy, Biocorrosion and Biofilms Lab, UFRGS, 99 Osvaldo Aranha Avenue s.615D, CEP: 90035-190, POA, RS (Brazil); Gaylarde, C.C. [Dept. of Biophisics, UFRGS POA, RS (Brazil)

    2004-08-01

    Storage tanks containing microbially contaminated diesel oil are susceptible to corrosion. This process may be evaluated electrochemically in the laboratory using simulated storage systems containing diesel oil and an aqueous phase. The simulated aqueous phase must supply mineral nutrients for microbial growth, together with adequate electrical conductivity, without, however, being too corrosive, so as to allow the aggressive nature of the microbial metabolites to be detected. In this investigation, microbial growth was measured in six electrically conductive media overlaid with metropolitan diesel oil containing an additive package. The microorganisms were the filamentous fungi, Hormoconis resinae, Paecilomyces variotii and Aspergillus fumigatus, the bacterium Bacillus subtilis and the yeast Candida silvicola, all previously isolated from contaminated diesel oil. After 60 days incubation with pure or mixed inocula of these microorganisms, pH, conductivity and viable microorganisms were measured. The electrochemical behaviour of carbon steel ASTM 283-93-C was determined in each of the six media (uninoculated) and in selected inoculated medium via measurements of open circuit potential and potentiostatic polarization curves. The uptake of phosphate (corrosion inhibitor), microbial growth, pH, conductivity and anodic and cathodic polarization curves were assessed in the water phase after 30 and 60 days of incubation with each single species Aspergillus fumigatus and Hormoconis resinae and with the consortium. The medium which proved most appropriate was Bushnell-Haas medium modified by the omission of chlorides, which allowed satisfactory microbial growth and had low aggressivity towards the steel. The performance of electrochemical tests in aerated, rather than deaerated, electrolyte solutions is suggested to be important to allow the detection of microbial influence on passive film formation and stability. (Abstract Copyright [2004], Wiley Periodicals, Inc.)

  16. Effective extraction of elastase from Bacillus sp. fermentation broth using aqueous two-phase system

    Institute of Scientific and Technical Information of China (English)

    XU Ying; HE Guo-qing; LI Jing-jun

    2005-01-01

    This paper presents the evaluation of an aqueous two-phase system (ATPS) for extracting elastase produced by Bacillus sp. EL31410. The elastase and cell partition behavior in polyethylene glycol (PEG)/salt systems was investigated. The suitable system for elastase extraction was PEG/KH2PO4-K2HPO4, in which elastase is mainly partitioned into the PEG-rich phase,while the cells remained in the other phase. The influence of defined system parameters (e.g. PEG molecular mass, pH, NaCl addition) on the partitioning behavior of elastase is described. The concentration of phase forming components, PEG and KH2PO4-K2HPO4, was optimized for elastase recovery by means of response surface methodology, and it was found that they greatly influenced extraction recovery. The optimal ATPS was 23.1% (w/w) PEG 2 000 and 11.7% (w/w) KH2PO4-K2HPO4. The predicted recovery was about 89.5%, so this process is suggested to be a rapid and convenient method for elastase extraction.

  17. CFD Analysis of Multi-Phase Reacting Transport Phenomena in Discharge Process of Non-Aqueous Lithium-Air Battery

    OpenAIRE

    Yuan, Jinliang; Yu, Jong-Sung; Sundén, Bengt

    2015-01-01

    A computational fluid dynamics (CFD) model is developed for rechargeable non-aqueous electrolyte lithium-air batteries with a partial opening for oxygen supply to the cathode. Multi-phase transport phenomena occurred in the battery are considered, including dissolved lithium ions and oxygen gas in the liquid electrolyte, solid-phase electron transfer in the porous functional materials and liquid-phase charge transport in the electrolyte. These transport processes are coupled with the electroc...

  18. Single step aqueous two-phase extraction for downstream processing of C-phycocyanin from Spirulina platensis

    OpenAIRE

    Chethana, S.; Nayak, Chetan A.; M.C. Madhusudhan; Raghavarao, K. S. M. S.

    2014-01-01

    C-phycocyanin, a natural food colorant, is gaining importance worldwide due to its several medical and pharmaceutical applications. In the present study, aqueous two-phase extraction was shown to be an attractive alternative for the downstream processing of C-phycocyanin from Spirulina platensis. By employing differential partitioning, C-phycocyanin selectively partitioned to the polymer rich (top) phase in concentrated form and contaminant proteins to the salt rich (bottom) phase. This resul...

  19. 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.

  20. Aqueous-phase behavior and vesicle formation of natural glycolipid biosurfactant, mannosylerythritol lipid-B.

    Science.gov (United States)

    Worakitkanchanakul, Wannasiri; Imura, Tomohiro; Fukuoka, Tokuma; Morita, Tomotake; Sakai, Hideki; Abe, Masahiko; Rujiravanit, Ratana; Chavadej, Sumaeth; Minamikawa, Hiroyuki; Kitamoto, Dai

    2008-08-01

    Mannosylerythritol lipids (MELs) are one of the most promising glycolipid biosurfactants produced by yeast strains of the genus Pseudozyma. In this study, the aqueous-phase behavior of a new monoacetyl MEL derivative, 1-O-beta-(2',3'-di-O-alka(e)noyl-6'-O-acetyl-d-mannopyranosyl)-d-erythritol (MEL-B), was investigated using polarized optical microscopy, small-angle X-ray scattering (SAXS), confocal laser scanning microscopy (CLSM), and differential scanning calorimetry (DSC). The present MEL-B was found to self-assemble into a lamellar (L(alpha)) phase over remarkably wide concentration and temperature ranges. According to SAXS measurement, the interlayer spacing (d) was estimated to be almost constant (about 4.7 nm) at the low MEL-B concentration (60 wt.%) region, the d-spacing gradually decreased to 3.1 nm with an increase in the MEL-B concentration. The thermal stability of the liquid crystalline phase was investigated by DSC measurement. The obtained L(alpha) phase was found to be stable up to 95 degrees C below a MEL-B concentration of 85 wt.%; then, the melting temperature of the liquid crystalline phase dramatically decreased with an increase in MEL-B concentration (above 85 wt.%). Furthermore, we found relatively large vesicles (1-5 microm) at the low MEL-B concentration using CLSM observation. The trapped volume of the obtained MEL-B vesicle was estimated to be about 0.42 microL/mumol by glucose dialysis method. These results suggest that the natural glycolipid biosurfactant, the newly found MEL-B, would be useful in various fields of applications as an L(alpha) phase- and/or vesicle-forming lipid. PMID:18456469

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2007-04-25

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

  2. A Novel Approach for Microencapsulation of Nanoemulsions to Overcome the Oxidation of Bioactives in Aqueous Phase

    Directory of Open Access Journals (Sweden)

    Haroon Jamshaid Qazi

    2015-02-01

    Full Text Available Microencapsulation is a promising technique to retain the physical attributes of nanoemulsions and to overcome the oxidation of bioactives that become more available to aqueous phase during emulsification. Purity Gum Ultra (PGU and Hi-CAP 100 (HiCap emulsified nanoemulsions of Clove Oil (CO co-encapsulated with Canola oil (CA and Medium Chain Triglyceride (MCT (5:5% v/v CO:CA and CO:MCT were prepared through high pressure homogenization. Microencapsulation of nanoemulsions was performed using Whey Protein Isolates (WPI under vacuum using freeze drying, which is considered as appropriate method for heat sensitive compounds. The reconstituted emulsions of microencapsulated powder had similar particle sizes as that of fresh nanoemulsions while uncoated showed a big increase (<400 nm. Oxidation of bioactives with and without CO, before and after freeze drying was investigated at different intervals during 60 days of storage at 4 and 25°C by Thiobarbituric Acid Reactive Substances (TBARS assay. Microencapsulated PGU-CO:CA showed minimum TBARS values compared to other emulsions. Gas chromatography analysis of microcapsules also showed higher retention of CO and lower content on the interphase for aqueous interaction. Conclusively, this study proposes a novel strategy using a freeze drying process to microencapsulate nanoemulsion.

  3. Detection of non-aqueous phase liquid contamination by SH-TE seismoelectrics: A computational feasibility study

    Science.gov (United States)

    Munch, Federico D.; Zyserman, Fabio I.

    2016-07-01

    In this work we propose a one dimensional numerical study of the seismoelectric signals produced in a fresh water aquifer contaminated by either light or dense non-aqueous phase liquids ((L/D)NAPLs), considering a pure SH-wave seismic source. We investigate the nature of the electromagnetic response generated at media interfaces, the so called Interface Response (IR), by comparing it with the electromagnetic field generated by a current sheet; wherefrom we are able to interpret that the source of the IR behaves as an electric current flowing along the interface, differently to what happens when the IR is originated by the action of a P-wave, where electric charge accumulation generates an electric dipole. We perform a parametric study to analyze how the presence of contaminants affects the IR, resorting to an effective media approach to compute mechanical and electromagnetic properties, and considering three different effective fluid-saturation dependent electrokinetic coupling coefficient models. We observe, as expected, that porosity plays an important role in the amplitude of the IRs. When considering different NAPL saturations, significant effects on the IRs are only seen when the thickness of the contaminated layer is above a threshold value, which depends on the present contaminant and the considered effective electrokinetic coupling coefficient model.

  4. The Distribution of Plutonium(Ⅲ,Ⅳ) Nitrate Between Dilute TBP/OK and Aqueous Phase

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The distribution of plutonium (Ⅲ, Ⅳ) nitrate between dilute TBP/OK and aqueous phase is systematically investigated. On the basis of the preparation and stabilization of Pu(Ⅲ, Ⅳ), the influences of the concentration of HNO3, Al(NO3)3, TBP and UO2(NO3)2 on the distribution ratio of them are studied at 25℃. The results indicate that the distribution ratio of Pu(Ⅳ) has a maximum while that of Pu(Ⅲ) increases with the concentration of HNO3. The distribution ratio of Pu(Ⅲ, Ⅳ) increases along with the concentration of Al(NO3)3 and TBP. The extraction reaction

  5. Softness and non-spherical shape define the phase behavior and the structural properties of lysozyme in aqueous solutions

    Science.gov (United States)

    Baumketner, A.; Melnyk, R.; Holovko, M. F.; Cai, W.; Costa, D.; Caccamo, C.

    2016-01-01

    In this study, Boltzmann inversion is applied in conjunction with molecular dynamics simulations to derive inter-molecular potential for protein lysozyme in aqueous solution directly from experimental static structure factor. The potential has a soft repulsion at short distances and an attraction well at intermediate distances that give rise to the liquid-liquid phase separation. Moreover, Gibbs ensemble Monte Carlo simulations demonstrate that a non-spherical description of lysozyme is better suited to correctly reproduce the experimentally observed properties of such a phase separation. Our findings shed new light on the common problem in molecular and cell biology: "How to model proteins in their natural aqueous environments?"

  6. Aqueous phase reforming of sorbitol to bio-gasoline over Ni/HZSM-5 catalysts

    International Nuclear Information System (INIS)

    Highlights: ► Development of an efficient bifunctional Ni/HZSM-5 catalyst for aqueous phase reforming of sorbitol. ► Optimizing the reaction process parameters for bio-gasoline production. ► Optimizing the interaction between Ni species and zeolite by calcination. -- Abstract: Liquid fuel such as bio-gasoline derived from biomass is widely recognized as a potential substitution for the diminishing fossil fuels due to its abundance of raw materials and lower greenhouse gas emissions. In this work, Ni/HZSM-5 catalysts were developed by incipient impregnation method and applied in the bio-gasoline production by aqueous phase reforming of sorbitol. The effects of reaction temperature, hydrogen pressure and calcination temperature of the catalysts on the catalytic performance were investigated. The activity test results showed that the catalyst calcined at 500 °C had the maximal activity with 47.6% of the bio-gasoline yield and 76.4% of the total selectivity of lighter alkanes (C5-C6) at 240 °C and 4.0 MPa. The catalysts were characterized by N2 physical adsorption, H2 temperature-programmed reduction (H2-TPR), H2 temperature-programmed desorption (H2-TPD), and infrared spectroscopy (IR) techniques. The characterization results revealed that the catalyst calcined at 500 °C can provide optimum surface area and pore volume for the reaction. Moreover, 100% of the reducibility of Ni species was detected on the surface of HZSM-5, following by more nickel active sites, which led to a visible increase in the yield of bio-gasoline.

  7. Online Investigation of Aqueous-Phase Electrochemical Reactions by Desorption Electrospray Ionization Mass Spectrometry

    Science.gov (United States)

    Lu, Mei; Liu, Yong; Helmy, Roy; Martin, Gary E.; Dewald, Howard D.; Chen, Hao

    2015-08-01

    Electrochemistry (EC) combined with mass spectrometry (MS) is a powerful tool for elucidation of electrochemical reaction mechanisms. However, direct online analysis of electrochemical reaction in aqueous phase was rarely explored. This paper presents the online investigation of several electrochemical reactions with biological relevance in the aqueous phase, such as nitrosothiol reduction, carbohydrate oxidation, and carbamazepine oxidation using desorption electrospray ionization mass spectrometry (DESI-MS). It was found that electroreduction of nitrosothiols [e.g., nitrosylated insulin B (13-23)] leads to free thiols by loss of NO, as confirmed by online MS analysis for the first time. The characteristic mass shift of 29 Da and the reduced intensity provide a quick way to identify nitrosylated species. Equally importantly, upon collision-induced dissociation (CID), the reduced peptide ion produces more fragment ions than its nitrosylated precursor ion (presumably the backbone fragmentation cannot compete with the facile NO loss for the precursor ion), thus facilitating peptide sequencing. In the case of saccharide oxidation, it was found that glucose undergoes electro-oxidation to produce gluconic acid at alkaline pH, but not at neutral and acidic pHs. Such a pH-dependent electrochemical behavior was also observed for disaccharides such as maltose and cellobiose. Upon electrochemical oxidation, carbamazepine was found to undergo ring contraction and amide bond cleavage, which parallels the oxidative metabolism observed for this drug in leucocytes. The mechanistic information of these redox reactions revealed by EC/DESI-MS would be of value in nitroso-proteome research and carbohydrate/drug metabolic studies.

  8. AQUEOUS TWO-PHASE GAS FLOATATION SPECTROPHOTOMETRIC DETERMINATION OF TRACE TETRACYCLINE IN ENVIRONMENTAL WATER SAMPLE

    Institute of Scientific and Technical Information of China (English)

    HOU Yanmin; YAN Yongsheng; LI Chunxiang; ZHAO Xiaojun; WANG Liang

    2008-01-01

    A green method for separating and enriching trace tetracycline (TC) in environment water by Aqueous Two-phase Gas Fioatation Spectrophotometry has been proposed, the principium was discussed.In this paper, the hydrophobic complex composed of Mg(Ⅱ) and TC was floated into organic phase under the optimal conditions: pH=10, the floatatlon equipment is home-made, n-propyl alcohol as the organic solvent, sodium chloride as the separating phase reagent.The data were obtained by spectrophotometry after floatatlon; The linear regression ,equation is A=2.33×105 C(mol/L)+0.2179, linear range is from 3.77×107mol/L to 6.32×105mol/L, respectively, with the correlation coefficient (r) better than 0.9997, relative recoveries is 99.7% to 100.3%, limit of detection was 4.29×10-8mol/L, The method can be applied to analyse the trace TC in water sample, the result is better.

  9. A novel procedure for phase separation in dispersive liquid-liquid microextraction based on solidification of the aqueous phase.

    Science.gov (United States)

    March, J G; Cerdà, V

    2016-08-15

    In this paper, an alternative for handling the organic phase after a dispersive liquid-liquid microextraction using organic solvents lighter than water is presented. It is based on solidification (at -18°C) of the aqueous phase obtained after centrifugation, and the decantation, collection and analysis of the liquid organic layer. The extraction of nicotine in toluene, and its determination in eggplant samples was conducted as a proof of concept. The study has been carried out using standards prepared in water and the formation of the dispersion was assisted by sonication. The organic extract was analysed using gas chromatography coupled to mass spectrometry. Satisfactory analytical figures of merit as: limit of detection (0.4µgL(-1), 2ngg(-1) wet sample), limit of quantification (1.2µgL(-1), 6.5ngg(-1) wet sample), within-day precision (RSD=7%), and linearity interval (up to 384µgL(-1) nicotine) were achieved. It constituted a contribution to the handling of organic extracts after microextraction processes. PMID:27260454

  10. Supercooling of aqueous dimethylsulfoxide solution at normal and high pressures: Evidence for the coexistence of phase-separated aqueous dimethylsulfoxide solutions of different water structures

    Science.gov (United States)

    Kanno, H.; Kajiwara, K.; Miyata, K.

    2010-05-01

    Supercooling behavior of aqueous dimethylsulfoxide (DMSO) solution was investigated as a function of DMSO concentration and at high pressures. A linear relationship was observed for TH (homogeneous ice nucleation temperature) and Tm (melting temperature) for the supercooling of aqueous DMSO solution at normal pressure. Analysis of the DTA (differential thermal analysis) traces for homogeneous ice crystallization in the bottom region of the TH curve for a DMSO solution of R =20 (R: moles of water/moles of DMSO) at high pressures supported the contention that the second critical point (SCP) of liquid water should exist at Pc2=˜200 MPa and at Tc2<-100 °C (Pc2: pressure of SCP, Tc2: temperature of SCP). The presence of two TH peaks for DMSO solutions (R =15, 12, and 10) suggests that phase separation occurs in aqueous DMSO solution (R ≤15) at high pressures and low temperatures (<-90 °C). The pressure dependence of the two TH curves for DMSO solutions of R =10 and 12 indicates that the two phase-separated components in the DMSO solution of R =10 have different liquid water structures [LDL-like and HDL-like structures (LDL: low-density liquid water, HDL: high-density liquid water)] in the pressure range of 120-230 MPa.

  11. Source separation and clustering of phase-locked subspaces.

    Science.gov (United States)

    Almeida, Miguel; Schleimer, Jan-Hendrik; Bioucas-Dias, José Mario; Vigário, Ricardo

    2011-09-01

    It has been proven that there are synchrony (or phase-locking) phenomena present in multiple oscillating systems such as electrical circuits, lasers, chemical reactions, and human neurons. If the measurements of these systems cannot detect the individual oscillators but rather a superposition of them, as in brain electrophysiological signals (electro- and magneoencephalogram), spurious phase locking will be detected. Current source-extraction techniques attempt to undo this superposition by assuming properties on the data, which are not valid when underlying sources are phase-locked. Statistical independence of the sources is one such invalid assumption, as phase-locked sources are dependent. In this paper, we introduce methods for source separation and clustering which make adequate assumptions for data where synchrony is present, and show with simulated data that they perform well even in cases where independent component analysis and other well-known source-separation methods fail. The results in this paper provide a proof of concept that synchrony-based techniques are useful for low-noise applications. PMID:21791409

  12. Secondary organic aerosol (trans)formation through aqueous phase guaiacol photonitration: a kinetic study

    Science.gov (United States)

    Kroflič, Ana; Grgić, Irena

    2014-05-01

    It is well known that atmospheric aerosols play a crucial role in the Earth's climate and public health (Pöschl 2005). Despite a great effort invested in the studies of secondary organic aerosol (SOA) budget, composition, and its formation mechanisms, there is still a gap between field observations and atmospheric model predictions (Heald et al. 2005, Hallquist et al. 2009, and Lim et al. 2010). The insisting uncertainties surrounding SOA formation and aging thus gained an increasing interest in atmospheric aqueous phase chemistry; they call for more complex and time consuming studies at the environmentally relevant conditions allowing confident extrapolation to desired ambient conditions. In addition to the adverse health effects of atmospheric particulate matter (PM) as such, toxicity is also attributed to nitro-aromatic and other organic compounds which have already been detected in real aerosol samples (Traversi et al. 2009). Moreover, low-volatility aromatic derivatives are believed to form at least partly in the aerosol aqueous phase and not only in the gas phase from where they partition into water droplets (Ervens et al. 2011). Two nitro derivatives of biomass burning tracer guaiacol have recently been found in winter PM10 samples from the city of Ljubljana, Slovenia, and aqueous photonitration reaction was proposed as their possible production pathway (Kitanovski et al. 2012). In this study the kinetics of guaiacol nitration in aqueous solution was investigated in the presence of H2O2 and NO2¯ upon simulated solar irradiation (Xenon lamp, 300 W). During the experiment the DURAN® flask with the reaction mixture was held in the thermostated bath and thoroughly mixed. The reaction was monitored for 44 hours at different temperatures. Guaiacol and its main nitro-products (4-nitroguaiacol, 4-NG; 6-nitroguaiacol, 6-NG; and 4,6-dinitroguaiacol, 4,6-DNG) were quantified in every aliquot, taken from the reaction mixture, by use of high pressure liquid

  13. Phase behavior of ABC-type triple-hydrophilic block copolymers in aqueous solutions.

    Science.gov (United States)

    Zheng, Lingfei; Wu, Jianqi; Wang, Zheng; Yin, Yuhua; Jiang, Run; Li, Baohui

    2016-07-01

    The phase behavior of symmetric ABC triple-hydrophilic triblock copolymers in concentrated aqueous solutions is investigated using a simulated annealing technique. Two typical cases, in which the hydrophilicity of the middle B-block is either stronger or weaker than that of the end A- and C-blocks, are studied. In these two cases, a variety of phase diagrams are constructed as a function of the volume fraction of the B-block and the copolymer concentration ([Formula: see text] for both non-frustrated and frustrated copolymers. Structures, such as two-color alternatingly packed cylinders or gyroid, and lamellae-in-lamellae etc. that do not occur in the melt system, are obtained in solutions. Rich phase transition sequences, especially re-entrant phase transitions involving complex continuous networks of alternating gyroid and alternating diamond are observed for a given copolymer with decreasing [Formula: see text] . The difference in hydrophilicity among different blocks can result in inhomogeneous distribution of solvent molecules in the morphology, and with the decrease of [Formula: see text] , the distribution of solvent molecules presents a non-monotonic variation. This results in a non-monotonic variation of the effective volume fraction of each domain with the decrease of [Formula: see text] , which induces the re-entrant phase transitions. The presence of a good solvent for all the blocks can cause changes in the effective segregation strengths between different blocks and also in chain conformations, hence can alter the bulk phases and results in the occurrence of new structures and phase transitions. Especially, structures having A-C interfaces or A-C mixed domains can be obtained even in the non-frustrated copolymer systems, and structures obtained in the frustrated systems may be similar to those obtained in the non-frustrated systems. The window of the alternating gyroid structures may occupy a large part of the phase diagram for non

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

    Science.gov (United States)

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

    2015-10-30

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

  15. Desulfurization of dibenzothiophene by a newly isolated Corynebacterium sp.ZD-1 in aqueous phase

    Institute of Scientific and Technical Information of China (English)

    WANG Miao-dong; LI Wei; WANG Da-hui; SHI Yao

    2004-01-01

    Sulfur emission through fuel combustion is a global problem because it is a major cause of acid rain. Crud oil contains many heterocyclic organic sulfur compounds, among which dibenzothiophene(DBT) and DBTs bearing alkyl substitutions usually are representative compounds. A strain was isolated from refinery sludge and identified as Corynebacterium ZD-1. The behavior of DBT degradation by ZD-1 in aqueous phase was investigated. Corynebacterium ZD-1 could metabolize DBT to 2-hydroxybiphenyl(2-HBP) as the dead-end metabolite through a sulfur-specific pathway. In shake flask culture, ZD-1 had its maximal desulfurization activity in the late exponential growth phase and the specific production rate of 2-HBP was about 0.14(mmol·kg dry cell-1·min-1, mmol·KDC-1·min-1). Active resting cells for desulfurization should be prepared only in this period. 2-HBP inhibited the growth of strain ZD-1, the production of DBT degradation enzymes, and the activity of enzymes. Sulfate inhibited the production of dibenzothiophene(DBT) degradation enzymes but had no effect on the enzymes' activity. The production rates of 2-HBP at lower cell densities were higher and the maximum amount conversion of DBT to 2-HBP(0.067 mmol/L) after 8 h was gained at 9.2(g dry cell/L) rather higher cell density. The results indicated that this newly isolated strain could be a promising biocatalyst for DBT desulfurization.

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

    Science.gov (United States)

    Flieger, J; Czajkowska-Żelazko, A

    2015-01-01

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

  17. Evolution of phase and morphology of titanium dioxide induced from peroxo titanate complex aqueous solution.

    Science.gov (United States)

    Chang, Jeong Ah; Vithal, Muga; Baek, In Chan; Seok, Sang Il

    2010-01-01

    We demonstrate the growth of anatase TiO2 in nanospheres and rutile TiO2 in nanorods, by the hydrolysis of titanium tetraisopropoxide (TTIP) in the presence of hydrogen peroxide at 100 degrees C using sol-gel method. X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), scanning electron microscopy (SEM), and surface area measurement techniques are used to characterize the phase and shape developments of TiO2 obtained from peroxo titanate complex in an aqueous solution at 100 degrees C. Peroxo titanate complexes were prepared by a reaction of titanium hydroxide, formed by hydrolysis of titanium tetraisopropoxide (TTIP), and different amounts of hydrogen peroxide (H2O2). TEM and XRD investigations reveal that the size of spheres (anatase) and rods (rutile) are about 8 nm (diameter) and about 13 x 29 nm approximately 20 x 75 nm (width x length) respectively. The influence of molar ratio of H2O2/TTIP on the phase and morphology of TiO2 is presented. A mixture of anatase spheres and short rutile rods are formed at low H2O2/TTIP ratio while predominantly rutile a quit long rods are formed at higher H2O2/TTIP ratio. PMID:20352827

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1997-12-31

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

  19. SINGLE - PHASE INVERTER CONTROL TECHNIQUES FOR INTERFACING RENEWABLE ENERGY SOURCES

    OpenAIRE

    C.Nallasivam

    2015-01-01

    A novel current control technique is proposed to control power flow from a renewable energy source feeding a microgrid system through a three - phase parallel - connected inverter. The parallel - connected inverter ensures that the power flow from the grid with low - current total harmonic distortion even in the presence of nonlinear load. The renewable energy sources ar e paralleled, and the average of this constant sup...

  20. 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.

  1. Recovery of acetic acid from an aqueous pyrolysis oil phase by reactive extraction using tri-n-octylamine

    NARCIS (Netherlands)

    Rasrendra, C. B.; Girisuta, B.; van de Bovenkamp, H. H.; Winkelman, J. G. M.; Leijenhorst, E. J.; Venderbosch, R. H.; Windt, M.; Meier, D.; Heeres, H. J.

    2011-01-01

    The application of reactive extraction to isolate organic acids, particularly acetic acid, from the aqueous stream of phase splitted pyrolysis oil using a long chain aliphatic tertiary amine is reported. Acetic acid recovery was optimized by selecting the proper amine and diluent combination and adj

  2. Regional Air Quality Model Application of the Aqueous-Phase Photo Reduction of Atmospheric Oxidized Mercury by Dicarboxylic Acids

    Science.gov (United States)

    In most ecosystems, atmospheric deposition is the primary input of mercury. The total wet deposition of mercury in atmospheric chemistry models is sensitive to parameterization of the aqueous-phase reduction of divalent oxidized mercury (Hg2+). However, most atmospheric chemistry...

  3. Stability and activity of carbon nanofiber-supported catalysts in the aqueous phase reforming of ethylene glycol

    NARCIS (Netherlands)

    Haasterecht, van T.; Ludding, C.C.I.; Jong, de K.P.; Bitter, J.H.

    2013-01-01

    Nickel, cobalt, copper and platinum nanoparticles supported on carbon nano-fibers were evaluated with respect to their stability, catalytic activity and selectivity in the aqueous phase reforming of ethylene glycol (230 ¿, autogenous pressure, batch reactor). The initial surface-specific activities

  4. Stability and activity of carbon nanofiber-supported catalysts in the aqueous phase reforming of ethylene glycol

    NARCIS (Netherlands)

    van Haasterecht, T.; Ludding, C.C.I.; de Jong, K.P.; Bitter, J.H.

    2013-01-01

    Nickel, cobalt, copper and platinum nanoparticles supported on carbon nano-fibers were evaluated with respect to their stability, catalytic activity and selectivity in the aqueous phase reforming of ethylene glycol (230 ◦C, autogenous pressure, batch reactor). The initial surface-specific activities

  5. Highly selective bimetallic Pt-Cu/Mg(Al)O catalysts for the aqueous-phase reforming of glycerol

    NARCIS (Netherlands)

    Boga, D.A.; Oord, R.; Beale, A.M.; Chung, Y.M.; Bruijnincx, P.C.A.; Weckhuysen, B.M.

    2013-01-01

    Monometallic Pt and bimetallic Pt-Cu catalysts supported on Mg(Al)O mixed oxides, obtained by calcination of the corresponding layered double hydroxides (LDHs), were prepared and tested in the aqueous-phase reforming (APR) of glycerol. The effect of the Mg/Al ratio and calcination temperature of the

  6. Is the HO4- anion a key species in the aqueous-phase decomposition of ozone?

    Science.gov (United States)

    Anglada, Josep M; Torrent-Sucarrat, Miquel; Ruiz-Lopez, Manuel F; Martins-Costa, Marilia

    2012-10-15

    The role of the HO(4)(-) anion in atmospheric chemistry and biology is a matter of debate, because it can be formed from, or be in equilibrium with, key species such as O(3) + HO(-) or HO(2) + O(2) (-). The determination of the stability of HO(4)(-) in water therefore has the greatest relevance for better understanding the mechanism associated with oxidative cascades in aqueous solution. However, experiments are difficult to perform because of the short-lived character of this species, and in this work we have employed DFT, CCSD(T) complete basis set (CBS), MRCI/aug-cc-pVTZ, and combined quantum mechanics/molecular mechanics (QM/MM) calculations to investigate this topic. We show that the HO(4)(-) anion has a planar structure in the gas phase, with a very large HOO-OO bond length (1.823 Å). In contrast, HO(4)(-) adopts a nonplanar configuration in aqueous solution, with huge geometrical changes (up to 0.232 Å for the HOO-OO bond length) with a very small energy cost. The formation of the HO(4)(-) anion is predicted to be endergonic by 5.53±1.44 and 2.14±0.37 kcal mol(-1) with respect to the O(3) + HO(-) and HO(2) + O(2)(-) channels, respectively. Moreover, the combination of theoretical calculations with experimental free energies of solvation has allowed us to obtain accurate free energies for the main reactions involved in the aqueous decomposition of ozone. Thus, the oxygen transfer reaction (O(3) + OH(-) → HO(2) + O(2)(-)) is endergonic by 3.39±1.80 kcal mol(-1), the electron transfer process (O(3) + O(2)(-) → O(3)(-) + O(2)) is exergonic by 31.53±1.05 kcal mol(-1), supporting the chain-carrier role of the superoxide ion, and the reaction O(3) + HO(2)(-) → OH + O(2)(-) + O(2) is exergonic by 12.78±1.15 kcal mol(-1), which is consistent with the fact that the addition of small amounts of HO(2)(-) (through H(2)O(2)) accelerates ozone decomposition in water. The combination of our results with previously reported thermokinetic data provides some

  7. Matrix supported tailored polymer for solid phase extraction of fluoride from variety of aqueous streams

    Energy Technology Data Exchange (ETDEWEB)

    Thakur, Neha; Kumar, Sanjukta A.; Wagh, D.N. [Analytical Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Das, Sadananda; Pandey, Ashok K. [Radiochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Kumar, Sangita D., E-mail: sangdk@barc.gov.in [Analytical Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Reddy, A.V.R. [Analytical Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India)

    2012-01-30

    Highlights: Black-Right-Pointing-Pointer Th complexed with poly (bis[2-(methacryloyloxy)-ethyl]phosphate) as tailored polymer membranes. Black-Right-Pointing-Pointer Membranes offered high capacity and selectivity for fluoride in aqueous media. Black-Right-Pointing-Pointer Quantitative uptake (80 {+-} 5%) of fluoride. Black-Right-Pointing-Pointer Fast sorption kinetics. Black-Right-Pointing-Pointer Reusability of polymer membranes. - Abstract: Fluoride related health hazards (fluorosis) are a major environmental problem in many regions of the world. It affects teeth; skeleton and its accumulation over a long period can lead to changes in the DNA structure. It is thus absolutely essential to bring down the fluoride levels to acceptable limits. Here, we present a new inorganic-organic hybrid polymer sorbent having tailored fixed-sites for fluoride sorption. The matrix supported poly (bis[2-(methacryloyloxy)-ethyl]phosphate) was prepared by photo-initiator induced graft-polymerization in fibrous and microporous (sheet) host poly(propylene) substrates. These substrates were conditioned for selective fluoride sorption by forming thorium complex with phosphate groups on bis[2-methacryloyloxy)-ethyl] phosphate (MEP). These tailored sorbents were studied for their selectivity towards fluoride in aqueous media having different chemical conditions. The fibrous sorbent was found to take up fluoride with a faster rate (15 min for Almost-Equal-To 76% sorption) than the sheet sorbent. But, the fluoride loading capacity of sheet sorbent (4320 mg kg{sup -1}), was higher than fibrous and any other sorbent reported in the literature so far. The sorbent developed in the present work was found to be reusable after desorption of fluoride using NaOH solution. It was tested for solid phase extraction of fluoride from natural water samples.

  8. Effect of Protonation on the Solution and Phase Behavior of Aqueous Sodium Myristate.

    Science.gov (United States)

    Wen; Franses

    2000-11-01

    Aqueous sodium myristate solutions have been shown to have unusually low dynamic tensions (1-10 mN/m) under pulsating area conditions. These solutions have no sharp solubility limit, evidently because they are protonated (or "hydrolyzed") to form the much less soluble myristic acid and acid soaps. With no added electrolytes, the protonation fraction is 1% or less. The apparent protonation equilibrium "constant" increases with increasing concentration, indicating strong solution nonidealities, in addition to micellization. This protonation seems to affect the solution and phase behavior of aqueous sodium myristate strongly, as evidenced by the effect of added NaOH. Ion-selective electrodes (for Na(+) and H(+)) and conductimetry indicate that at 25 degrees C dissolved surfactant concentrations keep increasing well after dispersed particles are observed (2 mM). A cmc of about 4.5 mM, micelles of aggregation number n=70 and counterion binding parameter beta=0.7 are inferred from these techniques. The cmc of sodium myristate increases slightly with temperature from 25 to 45 degrees C. FTIR analysis of the filtered particles indicates that the dispersed particles are mainly acid soaps for concentrations less than 6 mM. With 10 mM NaOH, the particles observed above 2 mM consist mostly of sodium myristate. From both conductivity and IR data, the solubility of sodium myristate in water at 25 degrees C is estimated to be about 6 mM, and as expected, it increases with increasing temperature and decreases with increasing sodium ion concentration. Copyright 2000 Academic Press.

  9. A Novel Aqueous Two Phase System Composed of Surfactant and Xylitol for the Purification of Lipase from Pumpkin (Cucurbita moschata Seeds and Recycling of Phase Components

    Directory of Open Access Journals (Sweden)

    Mehrnoush Amid

    2015-06-01

    Full Text Available Lipase is one of the more important enzymes used in various industries such as the food, detergent, pharmaceutical, textile, and pulp and paper sectors. A novel aqueous two-phase system composed of surfactant and xylitol was employed for the first time to purify lipase from Cucurbita moschata. The influence of different parameters such as type and concentration of surfactants, and the composition of the surfactant/xylitol mixtures on the partitioning behavior and recovery of lipase was investigated. Moreover, the effect of system pH and crude load on the degree of purification and yield of the purified lipase were studied. The results indicated that the lipase was partitioned into the top surfactant rich phase while the impurities partitioned into the bottom xylitol-rich phase using an aqueous two phase system composed of 24% (w/w Triton X-100 and 20% (w/w xylitol, at 56.2% of tie line length (TLL, (TTL is one of the important parameters in this study and it is determined from a bimodal curve in which the tie-line connects two nodes on the bimodal, that represent concentration of phase components in the top and bottom phases and a crude load of 25% (w/w at pH 8.0. Recovery and recycling of components was also measured in each successive step process. The enzyme was successfully recovered by the proposed method with a high purification factor of 16.4 and yield of 97.4% while over 97% of the phase components were also recovered and recycled. This study demonstrated that the proposed novel aqueous two phase system method is more efficient and economical than the traditional aqueous two phase system method for the purification and recovery of the valuable enzyme lipase.

  10. A Novel Aqueous Two Phase System Composed of Surfactant and Xylitol for the Purification of Lipase from Pumpkin (Cucurbita moschata) Seeds and Recycling of Phase Components.

    Science.gov (United States)

    Amid, Mehrnoush; Manap, Mohd Yazid; Hussin, Muhaini; Mustafa, Shuhaimi

    2015-06-17

    Lipase is one of the more important enzymes used in various industries such as the food, detergent, pharmaceutical, textile, and pulp and paper sectors. A novel aqueous two-phase system composed of surfactant and xylitol was employed for the first time to purify lipase from Cucurbita moschata. The influence of different parameters such as type and concentration of surfactants, and the composition of the surfactant/xylitol mixtures on the partitioning behavior and recovery of lipase was investigated. Moreover, the effect of system pH and crude load on the degree of purification and yield of the purified lipase were studied. The results indicated that the lipase was partitioned into the top surfactant rich phase while the impurities partitioned into the bottom xylitol-rich phase using an aqueous two phase system composed of 24% (w/w) Triton X-100 and 20% (w/w) xylitol, at 56.2% of tie line length (TLL), (TTL is one of the important parameters in this study and it is determined from a bimodal curve in which the tie-line connects two nodes on the bimodal, that represent concentration of phase components in the top and bottom phases) and a crude load of 25% (w/w) at pH 8.0. Recovery and recycling of components was also measured in each successive step process. The enzyme was successfully recovered by the proposed method with a high purification factor of 16.4 and yield of 97.4% while over 97% of the phase components were also recovered and recycled. This study demonstrated that the proposed novel aqueous two phase system method is more efficient and economical than the traditional aqueous two phase system method for the purification and recovery of the valuable enzyme lipase.

  11. A Novel Aqueous Two Phase System Composed of Surfactant and Xylitol for the Purification of Lipase from Pumpkin (Cucurbita moschata) Seeds and Recycling of Phase Components.

    Science.gov (United States)

    Amid, Mehrnoush; Manap, Mohd Yazid; Hussin, Muhaini; Mustafa, Shuhaimi

    2015-01-01

    Lipase is one of the more important enzymes used in various industries such as the food, detergent, pharmaceutical, textile, and pulp and paper sectors. A novel aqueous two-phase system composed of surfactant and xylitol was employed for the first time to purify lipase from Cucurbita moschata. The influence of different parameters such as type and concentration of surfactants, and the composition of the surfactant/xylitol mixtures on the partitioning behavior and recovery of lipase was investigated. Moreover, the effect of system pH and crude load on the degree of purification and yield of the purified lipase were studied. The results indicated that the lipase was partitioned into the top surfactant rich phase while the impurities partitioned into the bottom xylitol-rich phase using an aqueous two phase system composed of 24% (w/w) Triton X-100 and 20% (w/w) xylitol, at 56.2% of tie line length (TLL), (TTL is one of the important parameters in this study and it is determined from a bimodal curve in which the tie-line connects two nodes on the bimodal, that represent concentration of phase components in the top and bottom phases) and a crude load of 25% (w/w) at pH 8.0. Recovery and recycling of components was also measured in each successive step process. The enzyme was successfully recovered by the proposed method with a high purification factor of 16.4 and yield of 97.4% while over 97% of the phase components were also recovered and recycled. This study demonstrated that the proposed novel aqueous two phase system method is more efficient and economical than the traditional aqueous two phase system method for the purification and recovery of the valuable enzyme lipase. PMID:26091076

  12. Minimum-phase distribution of cosmic source brightness

    International Nuclear Information System (INIS)

    Minimum-phase distributions of brightness (profiles) for cosmic radio sources 3C 144 (the wave lambda=21 cm), 3C 338 (lambda=3.5 m), and 3C 353 (labda=31.3 cm and 3.5 m) are obtained. A real possibility for the profile recovery from module fragments of its Fourier-image is shown

  13. Equilibrium partial pressures, thermodynamic properties of aqueous and solid phases, and Cl{sub 2} production from aqueous HCl and HNO{sub 3} and their mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Massucci, M.; Clegg, S.L.; Brimblecombe, P. [Univ. of East Anglia, Norwich (United Kingdom). School of Environmental Sciences

    1999-05-27

    Equilibrium total pressures have been measured above aqueous HNO{sub 3} and aqueous HCl using a capacitance manometer. Equilibrium partial pressures of the acids have also been determined, by mass spectrometry, from 274.8 to 234.6 K for both HCl solutions, and from 265.0 to 240.1 K for 15.73 mol kg{sup {minus}1} HNO{sub 3}. Results are generally consistent with model predictions, though with small systematic deviations for the total pressure measurements over aqueous HCl at about 220 K. Mixtures of HCl{minus}HNO{sub 3}{minus}H{sub 2}O composition yielded measured total pressures orders of magnitude greater than predicted for the gases H{sub 2}O, HNO{sub 3}, and HCl. Mass spectrometric determinations and equilibrium thermodynamic calculations suggest that Cl{sub 2} and NOCl were produced by the reaction: 4H{sup +}{sub aq} + NO{sub 3}{sup {minus}}{sub aq} + 3Cl{sup {minus}}{sub aq} {r_equilibrium} NOCl{sub aq} + Cl{sub 2(aq)} + 2H{sub 2}O{sub (1)}, which is known to occur in aqua regia. Calculations for aqueous solutions of stratospheric aerosol composition suggest, purely on equilibrium grounds, that the reaction could be a source of active chlorine in the stratosphere. The correlation of Clegg and Brimblecombe of the thermodynamic properties of aqueous HNO{sub 3} activities has been revised, and vapor pressure products assessed from literature studies. The activity product for the reaction HNO{sub 3}{center_dot}2H{sub 2}O{sub (cr)} {r_equilibrium} H{sup +}{sub (aq)} + NO{sub 3}{sup {minus}}{sub (aq)} + 2H{sub 2}O{sub (1)} has also been determined. The model of Carslaw et al. has been revised for the solubility of HBr in aqueous H{sub 2}SO{sub 4} to stratospheric temperatures.

  14. Effects of aqueous humor hydrodynamics on human eye heat transfer under external heat sources.

    Science.gov (United States)

    Tiang, Kor L; Ooi, Ean H

    2016-08-01

    The majority of the eye models developed in the late 90s and early 00s considers only heat conduction inside the eye. This assumption is not entirely correct, since the anterior and posterior chambers are filled aqueous humor (AH) that is constantly in motion due to thermally-induced buoyancy. In this paper, a three-dimensional model of the human eye is developed to investigate the effects AH hydrodynamics have on the human eye temperature under exposure to external heat sources. If the effects of AH flow are negligible, then future models can be developed without taking them into account, thus simplifying the modeling process. Two types of external thermal loads are considered; volumetric and surface irradiation. Results showed that heat convection due to AH flow contributes to nearly 95% of the total heat flow inside the anterior chamber. Moreover, the circulation inside the anterior chamber can cause an upward shift of the location of hotspot. This can have significant consequences to our understanding of heat-induced cataractogenesis.

  15. Analysis of Solid and Aqueous Phase Products from Hydrothermal Carbonization of Whole and Lipid-Extracted Algae

    Directory of Open Access Journals (Sweden)

    Amber Broch

    2013-12-01

    Full Text Available Microalgae have tremendous potential as a feedstock for production of liquid biofuels, particularly biodiesel fuel via transesterification of algal lipids. However, biodiesel production results in significant amounts of algal residues, or “lipid extracted algae” (LEA. Suitable utilization of the LEA residue will improve the economics of algal biodiesel. In the present study, we evaluate the hydrothermal carbonization (HTC of whole and lipid extracted algal (Spirulina maxima feedstocks in order to produce a solid biofuel (hydrochar and value-added co-products in the aqueous phase. HTC experiments were performed using a 2-L Parr reactor (batch type at 175–215 °C with a 30-min holding time. Solid, aqueous and gaseous products were analyzed using various laboratory methods to evaluate the mass and carbon balances, and investigate the existence of high value chemicals in the aqueous phase. The HTC method is effective in creating an energy dense, solid hydrochar from both whole algae and LEA at lower temperatures as compared to lignocellulosic feedstocks, and is effective at reducing the ash content in the resulting hydrochar. However, under the treatment temperatures investigated, less than 1% of the starting dry algae mass was recovered as an identified high-value chemical in the aqueous phase.

  16. Exploring Feasibility for Application of Luminescent CdTe Quantum Dots Prepared in Aqueous Phase to Live Cell Imaging

    Institute of Scientific and Technical Information of China (English)

    Ji Fang WENG; Xing Tao SONG; Liang LI; Hui Feng QIAN; Ke Ying CHEN; Xue Ming XU; Cheng Xi CAO; Ji Cun REN

    2006-01-01

    This paper explored the feasibility for the application of luminescent CdTe quantum dots prepared in aqueous phase to live cell imaging. The highly luminescent CdTe quantum dots (QDs)were first prepared in aqueous phase, and then were covalently coupled to a plant lectin (UEA-1),as a fluorescent probe. After incubating with of human umbilical vein endothelial cells (HUVECs), the QD probe with UEA-1 was able to specifically bind the corresponding cell receptor. The good cell images were obtained in live cells using laser confocal scanning microscopy. We predict that QDs prepared in water phase will probably become an attractive alternative probe in cellular imaging and bio-labeling.

  17. Preparation of the multienzyme system gramicidin S-synthetase 2 with an aqueous three-phase system.

    Science.gov (United States)

    Kirchner, A; Simonis, M; von Döhren, H

    1987-06-19

    The distribution of gramicidin S-synthetase activity from disrupted cells suspended in aqueous two- and three-phase systems was investigated. An optimized three-phase system containing 5% dextran, 8% Ficoll, 11% PEG and 6.7% disrupted cells was found to be effective in extracting gramicidin S-synthetase activity. The activity yield achieved was higher in comparison to other preparation methods, and the subsequent purification steps were greatly facilitated. The time needed for the preparation of the labile gramicidin S-synthetase was considerably reduced. The combination of the aqueous phase extraction with chromatographic methods yielded 19 mg gramicidin S-synthetase 2 in essentially pure form from 30 g (wet weight) of cells.

  18. 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.

  19. ROLE OF TUNGSTEN IN THE AQUEOUS PHASE HYDRODEOXYGENATION OF ETHYLENE GLYCOL ON TUNGSTATED ZIRCONIA SUPPORTED PALLADIUM

    Energy Technology Data Exchange (ETDEWEB)

    Marin-Flores, Oscar G.; Karim, Ayman M.; Wang, Yong

    2014-11-15

    The focus of the present work was specifically on the elucidation of the role played by tungsten on the catalytic activity and selectivity of tungstated zirconia supported palladium (Pd-mWZ) for the aqueous phase hydrodeoxygenation (APHDO) of ethylene glycol (EG). Zirconia supported palladium (Pd-mZ) was used as reference. The catalysts were prepared via incipient wet impregnation and characterized using X-ray diffraction (XRD), temperature-programmed reduction (TPR), CO pulse chemisorption, CO-DRIFTS, ammonia temperature-programmed desorption (NH3-TPD) and pyridine adsorption. The presence of W results in larger Pd particles on supported Pd catalysts, i.e., 0.9 and 6.1 nm Pd particles are for Pd-mZ and Pd-mWZ, respectively. For comparison purposes, the activity of the catalytic materials used in this work was obtained using a well-defined set of operating conditions. The catalytic activity measurements show that the overall intrinsic activity of Pd particles on mWZ is 1.9 times higher than on mZ. APHDO process appears to be highly favored on Pd-mWZ whereas Pd-mZ exhibits a higher selectivity for reforming. This difference in terms of selectivity seems to be related to the high concentration of Brønsted acid sites and electron-deficient Pd species present on Pd-mWZ.

  20. Removal of Pb2+ ions in aqueous phase by a sodic Montmorillonite

    Directory of Open Access Journals (Sweden)

    Zoubida Lounis

    2012-03-01

    Full Text Available The sorption of Pb2+ ions in aqueous phase was carried out using sodium bentonite. The influence of the temperature and the pH on the capacity of the sorption and the percentage of the uptake of Pb2+ ions by sodium montmorillonite were studied. The sorption data were analysed in terms of the Freundlich and Langmuir isotherm models and the data fit the Langmuir sorption isotherm model well. Whereas, the thermodynamic parameters( the heat of adsorption Δ H°, the entropy Δ S° and the free energy ΔG° showed that the sorption is a phenomenon of exchange cation between adsorbat /adsorbent The negative value of ΔG° indicates that the sorption of Pb2+ ions on Na-Mt is spontaneous. The positive value of entropy ΔS° means that the disorder is at the interface solid-solution. The negative value of the heat of sorption ΔH° means that the process of elimination of Pb2+ ions is exothermic. However, it appears that the affinity sorption of Pb+2 ions on our clay decreases with increasing the temperature as the sorption capacity

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

    Directory of Open Access Journals (Sweden)

    Jan Åke Jönsson

    2011-10-01

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

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

    Institute of Scientific and Technical Information of China (English)

    WANG Yunqiang; SHAO Ming'an

    2009-01-01

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

  3. 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.

  4. Selective Synthesis and Advanced Characteristic of CdSe Semiconductor Quantum Dots by Aqueous Phase

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    This work mainly investigated the influences of some factors, such as, synthesis methods, pre cursor alternatives, and vacuum heat-treating process, etc, on the fluorescent characteristics of the semiconductor quantum dots synthesized by aqueous phase.The research results indicate that the fluorescent characteristic of water-solution sample prepared from Na2 SO3 precursor was sensitive to water bath heating time, and specially, its photoluminescence spectrum shows the unique phenomenon of double excitation and emission peaks.Meanwhile,the fluorescent characteristic of water- solution sample prepared from NaBH4 precursor is slightly influenced by water bath heating time, and the surface of CdSe quantum dots could be passivated by the excessive amount of NaBH4precursor, which results in the effective decrease of surface traps and great enhancement of quantum yield.Furthermore, the fluorescent emission peaks of samples could be sharpeued by vacuum heat-treating process, with its spectral full width at half of maximum (FWHM) around 30-40 nm, so the emission peaks become redshift, ofwhich the intensity greatly increases.

  5. Adsorption and solid phase extraction of 8-hydroxyquinoline from aqueous solutions by using natural bentonite

    International Nuclear Information System (INIS)

    The nitrogen-heterocyclic compound 8-hydroxyquinoline (8HQ) is one of the components of coal tar and has a wide variety of uses in industry. Because of its toxicity for aquatic organisms and harmful effects for human health, the removal of 8HQ from aqueous solutions by adsorption onto natural bentonite was investigated in the present work. The experimental results show that the optimum pH value of 2.5 is favourable for the 8HQ adsorption. The experimental data were fitted well with the pseudo-second-order kinetic and Langmuir adsorption isotherm models at all studied temperatures. The maximum adsorption capacity obtained from the Langmuir isotherm model at 20 deg. C was 120.6 mg g-1. The calculated thermodynamic results such as ΔGo (-24.3 kJ mol-1) and ΔHo (-9.56 kJ mol-1) indicate that the adsorption process is spontaneous and exothermic in nature. Solid phase extraction of 8HQ was also performed. The X-ray diffractometry (XRD), Fourier Transform Infrared (FTIR) and thermogravimetric (TG) analyses were carried out in order to confirm the 8HQ adsorption onto bentonite. According to the obtained results, natural bentonite can be a reusable and effective adsorbent for the removal of 8HQ.

  6. Aqueous two-phase systems strategies to establish novel bioprocesses for stem cells recovery.

    Science.gov (United States)

    González-González, Mirna; Rito-Palomares, Marco

    2014-12-01

    During the past decade, stem cell transplantation has emerged as a novel therapeutic alternative for several diseases. Nevertheless, numerous challenges regarding the recovery and purification steps must be addressed to supply the number of cells required and in the degree of purity needed for clinical treatments. Currently, there is a wide range of methodologies available for stem cells isolation. Nevertheless, there is not a golden standard method that accomplishes all requirements. A desirable recovery method for stem cells has to guarantee high purity and should be sensitive, rapid, quantitative, scalable, non- or minimally invasive to preserve viability and differentiation capacity of the purified cells. In this context, aqueous two-phase systems (ATPS) represent a promising alternative to fulfill the mentioned requirements, promoting the use of stem cell-based therapies for incurable diseases. This practical review focuses on presenting the bases for the development of a novel and scalable bioprocess for the purification of stem cells, with a case scenario of CD133(+) cells. The bioengineering strategies include the application of immunoaffinity ATPS in its multiple variants, including antibody-polymer conjugation, antibody addition and antibody immobilization. Conclusions are drawn in the light of the potential generic implementation of these strategies as an initial step in the establishment of bioprocesses for the purification of stem cells.

  7. Optical Detection of Aqueous Phase Analytes via Host-Guest Interactions on a Lipid Membrane Surface

    Energy Technology Data Exchange (ETDEWEB)

    Sasaki, D.Y.; Waggoner, T.A.

    1999-01-11

    The organization and assembly of molecules in cellular membranes is orchestrated through the recognition and binding of specific chemical signals. A simplified version of the cellular membrane system has been developed using a synthetically prepared membrane receptor incorporated into a biologically derived lipid bilayer. Through an interplay of electrostatic and van der Wards interactions, aggregation or dispersion of molecular components could be executed on command using a specific chemical signal. A pyrene fluorophore was used as an optical probe to monitor the aggregational state of the membrane receptors in the bilayer matrix. The pyrene excimer emission to monomer emission (E/M) intensity ratio gave a relative assessment of the local concentration of receptors in the membrane. Bilayers were prepared with receptors selective for the divalent metal ions of copper, mercury, and lead. Addition of the metal ions produced a rapid dispersion of aggregated receptor components at nano- to micro-molar concentrations. The process was reversible by sequestering the metal ions with EDTA. Receptors for proteins and polyhistidine were also prepared and incorporated into phosphatidylcholine lipid bilayers. In this case, the guest molecules bound to the membrane through multiple points of interaction causing aggregation of initially dispersed receptor molecules. The rapid, selective, and sensitive fluorescence optical response of these lipid assemblies make them attractive in sensor applications for aqueous phase metal ions and polypeptides.

  8. Aqueous Phase Photo-Oxidation of Succinic Acid: Changes in Hygroscopic Properties and Reaction Products

    Science.gov (United States)

    Hudson, P. K.; Ninokawa, A.; Hofstra, J.; de Lijser, P.

    2013-12-01

    Atmospheric aerosol particles have been identified as important factors in understanding climate change. The extent to which aerosols affect climate is determined, in part, by hygroscopic properties which can change as a result of atmospheric processing. Dicarboxylic acids, components of atmospheric aerosol, have a wide range of hygroscopic properties and can undergo oxidation and photolysis reactions in the atmosphere. In this study, the hygroscopic properties of succinic acid aerosol, a non-hygroscopic four carbon dicarboxylic acid, were measured with a humidified tandem differential mobility analyzer (HTDMA) and compared to reaction products resulting from the aqueous phase photo-oxidation reaction of hydrogen peroxide and succinic acid. Reaction products were determined and quantified using gas chromatography-flame ionization detection (GC-FID) and GC-mass spectrometry (GC-MS) as a function of hydrogen peroxide:succinic acid concentration ratio and photolysis time. Although reaction products include larger non-hygroscopic dicarboxylic acids (e.g. adipic acid) and smaller hygroscopic dicarboxylic acids (e.g. malonic and oxalic acids), comparison of hygroscopic growth curves to Zdanovskii-Stokes-Robinson (ZSR) predictions suggests that the hygroscopic properties of many of the product mixtures are largely independent of the hygroscopicity of the individual components. This study provides a framework for future investigations to fully understand and predict the role of chemical reactions in altering atmospheric conditions that affect climate.

  9. 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

  10. 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.

  11. Extraction and recovery of 2-butoxyethanol from aqueous phases containing high saline concentration

    Directory of Open Access Journals (Sweden)

    Katherine E. Manz

    2016-09-01

    Full Text Available Ethylene glycol monobutyl ether (EGBE, also known as 2-butoxyethanol (2-BE, has been identified as a contaminant in hydraulic fracturing fluids. In order to determine the presence of 2-BE in hydraulic fracturing chemical additives, a reliable method for recovering 2-BE from aqueous phases by liquid-liquid extraction combined with gas chromatography/mass spectrometry (GC/MS was established. The liquid-liquid extraction method was applied to samples matrices containing various amounts of salt. Using methylene chloride for liquid-liquid extraction in a sample to solvent ratio of 1:3, ≥99% 2-BE recovery may be achieved with less than 5% standard error. The limit of detection was determined to be 0.957 mg L−1 2-BE. Accuracy was determined to be 2.58% and precision was determined using the coefficient of variation, which was 3.5%. The method was used to recover 2-BE in a hydraulic fracturing chemical additive called Revert Flow and to quantify the weight percent of 2-BE in the chemical additive. Weight percent of two additional components of Revert Flow, D-limonene and 1-butoxy-2-propanol, were also determined. We also used the method to determine the abiotic of 2-BE in water, which was 5.55 days. The persistence of 2-BE in hydraulic fracturing fluid was also investigated and determined that 2-BE is more persistent in this environment.

  12. Phase-contrast microtomography with polychromatic sealed source

    International Nuclear Information System (INIS)

    Conventional X-ray microradiography and microtomography are based on X-ray attenuation inside an object. For light objects (in the terms of X-ray absorption) much better way would be to use phase contrast, rather than attenuation contrast. Recently it has been shown that one can obtain phase by using a polychromatic source provided the focal spot size and detector resolution are small enough to maintain sufficient spatial coherence. The technique opens perspectives for high-resolution micro-CT for the objects with low X-ray attenuation, such as diamonds, biomedical objects, etc

  13. Concurrence of aqueous and gas phase contamination of groundwater in the Wattenberg oil and gas field of northern Colorado.

    Science.gov (United States)

    Li, Huishu; Son, Ji-Hee; Carlson, Kenneth H

    2016-01-01

    The potential impact of rapid development of unconventional oil and natural gas resources using hydraulic fracturing and horizontal drilling on regional groundwater quality has received significant attention. Major concerns are methane or oil/gas related hydrocarbon (such as TPHs, BTEX including benzene, toluene, ethybenzene and xylene) leaks into the aquifer due to the failure of casing and/or stray gas migration. Previously, we investigated the relationship between oil and gas activity and dissolved methane concentration in a drinking water aquifer with the major finding being the presence of thermogenic methane contamination, but did not find detectable concentrations of TPHs or BTEX. To understand if aqueous and gas phases from the producing formation were transported concurrently to drinking water aquifers without the presence of oil/gas related hydrocarbons, the ionic composition of three water groups was studied: (1) uncontaminated deep confined aquifer, (2) suspected contaminated groundwater - deep confined aquifer containing thermogenic methane, and (3) produced water from nearby oil and gas wells that would represent aqueous phase contaminants. On the basis of quantitative and spatial analysis, we identified that the "thermogenic methane contaminated" groundwater did not have similarities to produced water in terms of ionic character (e.g. Cl/TDS ratio), but rather to the "uncontaminated" groundwater. The analysis indicates that aquifer wells with demonstrated gas phase contamination have not been contacted by an aqueous phase from oil and gas operations according to the methodology we use in this study and the current groundwater quality data from COGCC. However, the research does not prove conclusively that this the case. The results may provide insight on contamination mechanisms since improperly sealed well casing may result in stray gas but not aqueous phase transport.

  14. Phase contrast imaging simulation and measurements using polychromatic sources with small source-object distances

    International Nuclear Information System (INIS)

    Phase contrast imaging is a technique widely used in synchrotron facilities for nondestructive analysis. Such technique can also be implemented through microfocus x-ray tube systems. Recently, a relatively new type of compact, quasimonochromatic x-ray sources based on Compton backscattering has been proposed for phase contrast imaging applications. In order to plan a phase contrast imaging system setup, to evaluate the system performance and to choose the experimental parameters that optimize the image quality, it is important to have reliable software for phase contrast imaging simulation. Several software tools have been developed and tested against experimental measurements at synchrotron facilities devoted to phase contrast imaging. However, many approximations that are valid in such conditions (e.g., large source-object distance, small transverse size of the object, plane wave approximation, monochromatic beam, and Gaussian-shaped source focal spot) are not generally suitable for x-ray tubes and other compact systems. In this work we describe a general method for the simulation of phase contrast imaging using polychromatic sources based on a spherical wave description of the beam and on a double-Gaussian model of the source focal spot, we discuss the validity of some possible approximations, and we test the simulations against experimental measurements using a microfocus x-ray tube on three types of polymers (nylon, poly-ethylene-terephthalate, and poly-methyl-methacrylate) at varying source-object distance. It will be shown that, as long as all experimental conditions are described accurately in the simulations, the described method yields results that are in good agreement with experimental measurements

  15. Phase contrast imaging simulation and measurements using polychromatic sources with small source-object distances

    Science.gov (United States)

    Golosio, Bruno; Delogu, Pasquale; Zanette, Irene; Carpinelli, Massimo; Masala, Giovanni Luca; Oliva, Piernicola; Stefanini, Arnaldo; Stumbo, Simone

    2008-11-01

    Phase contrast imaging is a technique widely used in synchrotron facilities for nondestructive analysis. Such technique can also be implemented through microfocus x-ray tube systems. Recently, a relatively new type of compact, quasimonochromatic x-ray sources based on Compton backscattering has been proposed for phase contrast imaging applications. In order to plan a phase contrast imaging system setup, to evaluate the system performance and to choose the experimental parameters that optimize the image quality, it is important to have reliable software for phase contrast imaging simulation. Several software tools have been developed and tested against experimental measurements at synchrotron facilities devoted to phase contrast imaging. However, many approximations that are valid in such conditions (e.g., large source-object distance, small transverse size of the object, plane wave approximation, monochromatic beam, and Gaussian-shaped source focal spot) are not generally suitable for x-ray tubes and other compact systems. In this work we describe a general method for the simulation of phase contrast imaging using polychromatic sources based on a spherical wave description of the beam and on a double-Gaussian model of the source focal spot, we discuss the validity of some possible approximations, and we test the simulations against experimental measurements using a microfocus x-ray tube on three types of polymers (nylon, poly-ethylene-terephthalate, and poly-methyl-methacrylate) at varying source-object distance. It will be shown that, as long as all experimental conditions are described accurately in the simulations, the described method yields results that are in good agreement with experimental measurements.

  16. Chemical characterization of SOA formed from aqueous-phase reactions of phenols with the triplet excited state of carbonyl and hydroxyl radical

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Lu; Smith, Jeremy; Laskin, Alexander; Anastasio, Cort N.; Laskin, Julia; Zhang, Qi

    2014-01-01

    Phenolic compounds, which are emitted in significant amounts from biomass burning, can undergo fast reactions in atmospheric aqueous phases to form secondary organic aerosol (aqSOA). In this study, we investigate the reactions of phenol and two methoxy-phenols (syringol and guaiacol) with two major aqueous phase oxidants – the triplet excited states of an aromatic carbonyl (3C*) and hydroxyl radical (•OH). We thoroughly characterize the low-volatility species produced from these reactions and interpret their formation mechanisms using aerosol mass spectrometry (AMS), desorption electrospray ionization mass spectrometry (DESIMS), and ion chromatography (IC). A large number of oxygenated molecules are identified, including oligomers containing up to six monomer units, functionalized monomer and oligomers with carbonyl, carboxyl, and hydroxyl groups, and small organic acid anions (e.g., formate, acetate, oxalate, and malate). The average atomic oxygen-to-carbon (O/C) ratios of phenolic aqSOA are in the range of 0.85-1.23, similar to those of low-volatility oxygenated organic aerosol (LV-OOA) observed in ambient air. The aqSOA compositions are overall similar for the same precursor, but the reactions mediated by 3C* are faster than •OH-mediated reactions and produce more oligomers and hydroxylated species at the point when 50% of the phenol had reacted. Profiles determined using a thermodenuder indicate that the volatility of phenolic aqSOA is influenced by both oligomer content and O/C ratio. In addition, the aqSOA shows enhanced light absorption in the UV-vis region, suggesting that aqueous-phase reactions of phenols are likely an important source of brown carbon in the atmosphere, especially in regions influenced by biomass burning.

  17. Influence of non-aqueous phase liquid configuration on induced polarization parameters: Conceptual models applied to a time-domain field case study

    Science.gov (United States)

    Johansson, Sara; Fiandaca, Gianluca; Dahlin, Torleif

    2015-12-01

    Resistivity and induced polarization (IP) measurements on soil contaminated with non-aqueous phase liquids (NAPLs) show a great variety in results in previous research. Several laboratory studies have suggested that the presence of NAPLs in soil samples generally decrease the magnitude of the IP-effect, while others have indicated the opposite. A number of conceptual models have been proposed suggesting that NAPLs can alter the pore space in different ways, e.g. by coating the grain surfaces and thus inhibiting grain polarization, or by changing the pore throat size and thus affecting the membrane polarization mechanism. The main aim of this paper is to review previously published conceptual models and to introduce some new concepts of possible residual NAPL configurations in the pore space. Time domain induced polarization measurements were performed at a NAPL contaminated field site, and the data were inverted using the Constant Phase Angle (CPA) model and the Cole-Cole model respectively. No significant phase anomalies were observed in the source area of the contamination when the CPA inverted profiles were compared with soil sampling results of free-phase contaminant concentrations. However, relatively strong phase and normalized phase anomalies appeared next to the source area, where residual free-phase presence could be expected according to the chemical data. We conclude that depending on the NAPL configuration, different spectral IP responses can be expected. In previous research, the NAPL configurations in different samples or field sites are often unknown, and this may to some extent explain why different results have been achieved by different authors. In our field case, we believe that the NAPL forms a more or less continuous phase in the pore space of the source zone leading to an absence of IP anomalies. The increase in phase and normalized phase angle observed next to the source zone is interpreted as a degradation zone. The ongoing biodegradation

  18. Successful removal of p-quinone with chitosan in an aqueous phase in relation to degree of deacetylation.

    Science.gov (United States)

    Takahashi, Tomoki; Imai, Masanao; Suzuki, Isao

    2004-01-01

    Phenol oxidant is successfully removed by using chitosan particles in the aqueous phase. Removal of p-quinone by chitosan from crab shells was investigated kinetically from molecular weight (MW) of chitosan, deacetylation degree (DD) and reaction temperature. The rate constant assuming first-ordered reaction on removal of p-quinone in aqueous phase primarily depended on the MW of chitosan, not on the DD. Quantities of chitosan exceeding 5 x 10(5) MW are able to obtain a sufficiently high rate constant (10(-3) s(-1)). At higher temperatures, higher rate constants were obtained in the entire experimental MW and DD. The activation energy obtained was 43.8 kJ x mol(-1).

  19. 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...

  20. 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...

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

    Science.gov (United States)

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

    2006-10-01

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

  2. Crystallization processes of hydrous metal oxides in the presence of aqueous-phase

    International Nuclear Information System (INIS)

    Evaluation of solubility-limiting solid is a central theme for predicting the rate of radionuclide release from HLW repository to the accessible environment. Such solids which control the concentration of radionuclide in subsurface water are considered to be sparingly soluble hydrous oxides. However, most of the hydrous oxides are thermodynamically unstable and alter from the amorphous form into crystal (oxyhydroxide or oxide), which, in turn, changes the solubility of radionuclide drastically. So far, such crystallization rates have been hardly clarified. This co-operative research focused on (1) the crystallization process from amorphous Fe(OH)3 to goethite, i.e., α-FeO(OH), and (2) the precipitation of Ce(III) or Ce(IV) and the chemical change in ageing. To begin with, the method to determine the crystallization fraction has been developed for the study. This method using TG(thermogravimetry)-curve quantifies the mole fraction of crystalline hydrous oxides, e.g., (Fe in goethite)/(total Fe in hydrous iron oxides precipitated). Using this method, the crystallization process of Fe(OH)3 was examined. The experimental parameters were the ageing time, pH-value, temperature, and dehydration methods. The results suggested that the aqueous phase plays an important role in changing the chemical structure into the crystal form. This tendency was observed also in the hydrous oxides of Ce(III) and Ce(IV). Further, the crystallization rate of Ce(OH)4 to CeO2 depended on the initial amount of CeO2 in ageing (although its amount of CeO2 was relatively small as compared to Ce(OH)4). These information will contribute to predicting the solubility-limiting solid in the performance assessment of HLW repository system. (author)

  3. Removal of Nitrate in the Aqueous Phase Using Granular Ferric Hydroxide

    Directory of Open Access Journals (Sweden)

    Dehghani

    2015-04-01

    Full Text Available Background In recent years, the nitrate concentration in surface water and especially in groundwater was increased significantly in many parts of Iran. Objectives The main objectives of this study were to evaluate the feasibility of using granular ferric hydroxide (GFH to remove nitrate from aqueous phase as well as to determine the removal efficiency at the optimal condition. Materials and Methods The present study was conducted on a bench scale experiment. The spectrophotometer DR5000 (wavelength 520 nm was used to determine the nitrate concentration. The effect of influencing parameters including pH at 5 levels (3.8 - 7.8, initial nitrate concentration at 4 levels (50 - 150 mg/L the amount of adsorbent dose (0.625, 1.25, 2.5, 3.75 g/50mL, the effects of interfering ions, such as sulfate ions at 4 levels (200 - 800 mg/L and chloride ions at 4 levels (200 - 800 mg/L, and contact time at 3 levels (30 - 90 minutes were studied. Results Based on our data, pH of 4.8, adsorbent dose of 3.75 g and contact time of 90 minutes is optimal for nitrate removal. Furthermore, the nitrate reduction rate was increased rapidly by the addition of the adsorbent and decreased by nitrate addition. The nitrate reduction rate was increased by increasing the contact time. The percent of nitrate reduction was significantly enhanced by decreasing the pH (from 7.8 to 8.4 and then reached a plateau with a relative slow equilibration. Moreover, adsorption efficiency was significantly decreased in the presence of interfering ions, such as sulfate and chloride ions. Conclusions In conclusion, GFH can be used as a reliable and appropriate method with high efficiency for the reduction of nitrate in many polluted water resources.

  4. Formation and characteristics of aqueous two-phase systems formed by a cationic surfactant and a series of ionic liquids.

    Science.gov (United States)

    Wei, Xi-Lian; Wang, Xiu-Hong; Ping, A-Li; Du, Pan-Pan; Sun, De-Zhi; Zhang, Qing-Fu; Liu, Jie

    2013-11-15

    Aqueous two-phase systems (ATPS) were obtained in the aqueous mixtures of a cationic surfactant and a series of ionic liquids (ILs). The effects of IL structure, temperature and additives on the phase separation were systematically investigated. The microstructures of some ATPS were observed by freeze-fracture replication technique. Lyotropic liquid crystal was found in the bottom phase besides micelles under different conditions. Remarkably, both IL structure and additives profoundly affected the formation and properties of the ATPSs. The phase separation can be attributed to the existence of different aggregates and the cation-π interactions of the cationic surfactant with the ILs, which has a significant role in the formation of ATPS. The extraction capacity of the studied ATPS was also evaluated through their application in the extraction of two biosubstances. The results indicate that the ILs with BF4(-) as anion show much better extraction efficiencies than the corresponding ILs with Br(-) as anion do under the same conditions. l-Tryptophan was mainly distributed into the NPTAB-rich phase, while methylene blue and capsochrome were mainly in the IL-rich phase.

  5. Chemical characterization of the main secondary organic aerosol (SOA products formed through aqueous-phase photonitration of guaiacol

    Directory of Open Access Journals (Sweden)

    Z. Kitanovski

    2014-04-01

    Full Text Available Guaiacol (2-methoxyphenol and its derivatives can be emitted into the atmosphere by thermal degradation (i.e. burning of wood lignins. Due to its volatility, guaiacol is predominantly distributed in the atmospheric gaseous phase. Recent studies have shown the importance of aqueous-phase reactions in addition to the dominant gas-phase and heterogeneous reactions of guaiacol, in the formation of secondary organic aerosol (SOA in the atmosphere. The main objectives of the present study were to chemically characterize the low-volatility SOA products of the aqueous-phase photonitration of guaiacol and examine their possible presence in urban atmospheric aerosols. The aqueous-phase reactions were carried out under simulated sunlight and in the presence of H2O2 and nitrite. The formed guaiacol reaction products were concentrated by using solid-phase extraction (SPE and then purified by means of semi-preparative high-performance liquid chromatography (HPLC. The fractionated individual compounds were isolated as pure solids and further analyzed with liquid-state 1H, 13C and 2D nuclear magnetic resonance (NMR spectroscopy and direct infusion negative ion electrospray ionization tandem mass spectrometry ((–ESI-MS/MS. The NMR and product ion (MS2 spectra were used for unambiguous product structure elucidation. The main products of guaiacol photonitration are 4-nitroguaiacol (4NG, 6-nitroguaiacol (6NG, and 4,6-dinitroguaiacol (4,6DNG. Using the isolated compounds as standards, 4NG and 4,6DNG were unambiguously identified in winter PM10 aerosols from the city of Ljubljana (Slovenia by means of HPLC/(–ESI-MS/MS. Owing to the strong absorption of UV and visible light, 4,6DNG could be an important constituent of atmospheric "brown" carbon, especially in regions affected by biomass burning.

  6. Using radon as environmental tracer for the assessment of subsurface non-aqueous phase liquid (NAPL) contamination - a review

    International Nuclear Information System (INIS)

    The radioactive noble gas radon has an ambivalent nature: on one hand it is of main concern with regard to radiation protection, on the other hand it can be applied as powerful tracer tool in various fields of applied geosciences. Due to its omnipresence in nature, its chemical and physical properties, and its uncomplicated detectability radon fulfils all requirements for being used as environmental tracer. This application is discussed in the paper with focus on the use of radon as tracer for subsurface contamination with Non-Aqueous Phase Liquids (NAPL). After a short introduction in the ambivalence and ubiquitous presence of radon in nature, the theoretical background of its suitability as NAPL tracer is summarized. Finally three potential applications are discussed. Background information and practical examples are given for (i) the investigation of residual NAPL contamination in soils, (ii) the investigation of residual NAPL contamination in aquifers and (iii) the monitoring of the remediation of dissolved NAPL contamination in groundwater. The presented information reveals that radon is an ideal tracer for the assessment of a wide range of subsurface NAPL contamination. Still, its application is not without restrictions. Problems may occur due to mineralogical heterogeneity of the soil or aquifer matrix. Furthermore, local changes in the permeability of the subsurface may be associated with preferential groundwater or soil gas flow paths bypassing isolated sub-domains of an investigated NAPL source zone. Moreover, NAPL aging may result in alterations in the composition of a complex NAPL mixture thus giving rise to significant changes of the radon partition coefficient between NAPL and water or soil gas. However, since radon shows a strong affinity to NAPLs in general, semi-quantitative results will always be possible. (author)

  7. Studies of efficiency in a perforated rotating disc contactor using a polymer-polymer aqueous two-phase systems

    Directory of Open Access Journals (Sweden)

    L. A. Sarubbo

    2005-09-01

    Full Text Available The mass transfer process in a perforated rotating disc contactor (PRDC using a polymer-polymer aqueous two-phase system was investigated. The results show that the efficiency did not show a regular trend with the increase of the dispersed phase velocity and increased with the rotation velocity. The separation efficiency was higher for three rotating discs than for four discs. The increase in tie-line length decreased the efficiency. The separation efficiency reached high values, about 96% under conditions studied in this work.

  8. Phase 2 safety analysis report: National Synchrotron Light Source

    International Nuclear Information System (INIS)

    The Phase II program was established in order to provide additional space for experiments, and also staging and equipment storage areas. It also provides additional office space and new types of advanced instrumentation for users. This document will deal with the new safety issues resulting from this extensive expansion program, and should be used as a supplement to BNL Report No. 51584 ''National Synchrotron Light Source Safety Analysis Report,'' July 1982 (hereafter referred to as the Phase I SAR). The initial NSLS facility is described in the Phase I SAR. It comprises two electron storage rings, an injection system common to both, experimental beam lines and equipment, and office and support areas, all of which are housed in a 74,000 sq. ft. building. The X-ray Ring provides for 28 primary beam ports and the VUV Ring, 16. Each port is capable of division into 2 or 3 separate beam lines. All ports receive their synchrotron light from conventional bending magnet sources, the magnets being part of the storage ring lattice. 4 refs

  9. Surface waters as a sink and source of atmospheric gas phase ethanol.

    Science.gov (United States)

    Avery, G Brooks; Foley, Laura; Carroll, Angela L; Roebuck, Jesse Alan; Guy, Amanda; Mead, Ralph N; Kieber, Robert J; Willey, Joan D; Skrabal, Stephen A; Felix, J David; Mullaugh, Katherine M; Helms, John R

    2016-02-01

    This study reports the first ethanol concentrations in fresh and estuarine waters and greatly expands the current data set for coastal ocean waters. Concentrations for 153 individual measurements of 11 freshwater sites ranged from 5 to 598 nM. Concentrations obtained for one estuarine transect ranged from 56 to 77 nM and levels in five coastal ocean depth profiles ranged from 81 to 334 nM. Variability in ethanol concentrations was high and appears to be driven primarily by photochemical and biological processes. 47 gas phase concentrations of ethanol were also obtained during this study to determine the surface water degree of saturation with respect to the atmosphere. Generally fresh and estuarine waters were undersaturated indicating they are not a source and may be a net sink for atmospheric ethanol in this region. Aqueous phase ethanol is likely converted rapidly to acetaldehyde in these aquatic ecosystems creating the undersaturated conditions resulting in this previously unrecognized sink for atmospheric ethanol. Coastal ocean waters may act as either a sink or source of atmospheric ethanol depending on the partial pressure of ethanol in the overlying air mass. Results from this study are significant because they suggest that surface waters may act as an important vector for the uptake of ethanol emitted into the atmosphere including ethanol from biofuel production and usage.

  10. Testing the Performance of W-phase Source Inversion

    Science.gov (United States)

    Rivera, L.; Kanamori, H.

    2008-12-01

    We have recently developed a method to perform fast source parameter inversions for large earthquakes using the W-phase, a very long-period phase starting right after the P-wave arrival (Kanamori and Rivera, 2008). Here we report on the results of a systematic test on the performance of the method for seismic tsunami warning purposes. We tested it using a global data set of all Mw ≥ 7.0 earthquakes between 1990 and 2008 (240 events). We use the vertical VBB data from GSN and Geoscope stations (mainly STS-1 seismometers) filtered between 0.001 and 0.005 Hz. The window length, τ, used for inversion is distance dependent, τ= 15 Δ sec (Δ in degree). Typically we use stations up to 40°- 60° corresponding to a delay of 18-25 min after the origin time. To perform inversion, we need, in addition to the seismic traces, estimates of the hypocenter parameters and of the centroid delay. The PDE parameters, which are quickly available, can be used as a first approximation of the hypocenter location. The centroid source delay is first estimated from an approximate Mw determined from the W phase amplitudes. Having a database of pre-computed Green's functions, the actual inversion process is nearly instantaneous. We can improve the inversion using either grid search or parameter optimization by a non- linear least squares method. In the test reported here, we systematically use the Harvard or the Global CMT solution as reference. Specifically, we compare our solutions with the reference solutions, in terms of the seismic moment (i.e., Mw) and the orientation of the nodal planes. The results of comparison are encouraging. The differences in Mw between the W phase and the CMT inversions are 0.1 or smaller. The differences in the angular distance between the nodal planes are typically less than 5-10 deg. The solutions are in general robust. Because of the sparse station coverage, the solutions for older events (~ 1990-1992) are not constrained well, but are still adequate for

  11. Study of Phase Separation of Poly(N-isopropylacrylamide-co-styrene) Aqueous Solutions with Rayleigh Scattering Technique

    Institute of Scientific and Technical Information of China (English)

    Yi Guobin; Zhu Zhenghong; Wang Fei; Chen Xudong; Yang Jin; Huang Yunwei

    2011-01-01

    A thermally sensitive copolymer, poly(N-isopropylacrylamfide-co-styrene) [P(NIPAM-co-St)] (Mn=9.5×105 g/mol and Mw/Mn= 1.51) was synthesized by soap-free emulsion polymerization. The phase separation of the co-polymer in water was investigated by Rayleigh scattering (RS) technique. The RS spectra revealed the transition of molecular conformation and the aggregation of molecular chains in the course of phase separation. The coil-to-globule and globule-to-coil transitions of P(NIPAM-co-St) chains were found in one heating-and-cooling cycle. By means of Avrami formula, apparent activation energy of phase separation of P(NIPAM-co-St) aqueous solutions was estimated. Moreover, a model was proposed to describe the phase separation process.

  12. Nighttime aqueous-phase secondary organic aerosols in Los Angeles and its implication for fine particulate matter composition and oxidative potential

    Science.gov (United States)

    Saffari, Arian; Hasheminassab, Sina; Shafer, Martin M.; Schauer, James J.; Chatila, Talal A.; Sioutas, Constantinos

    2016-05-01

    Recent investigations suggest that aqueous phase oxidation of hydrophilic organic compounds can be a significant source of secondary organic aerosols (SOA) in the atmosphere. Here we investigate the possibility of nighttime aqueous phase formation of SOA in Los Angeles during winter, through examination of trends in fine particulate matter (PM2.5) carbonaceous content during two contrasting seasons. Distinctive winter and summer trends were observed for the diurnal variation of organic carbon (OC) and secondary organic carbon (SOC), with elevated levels during the nighttime in winter, suggesting an enhanced formation of SOA during that period. The nighttime ratio of SOC to OC was positively associated with the relative humidity (RH) at high RH levels (above 70%), which is when the liquid water content of the ambient aerosol would be high and could facilitate dissolution of hydrophilic primary organic compounds into the aqueous phase. Time-integrated collection and analysis of wintertime particles at three time periods of the day (morning, 6:00 a.m.-9:00 a.m.; afternoon, 11:00 a.m.-3:00 p.m.; night, 8:00 p.m.-4:00 a.m.) revealed higher levels of water soluble organic carbon (WSOC) and organic acids during the night and afternoon periods compared to the morning period, indicating that the SOA formation in winter continues throughout the nighttime. Furthermore, diurnal trends in concentrations of semi-volatile organic compounds (SVOCs) from primary emissions showed that partitioning of SVOCs from the gas to the particle phase due to the decreased nighttime temperatures cannot explain the substantial OC and SOC increase at night. The oxidative potential of the collected particles (quantified using a biological macrophage-based reactive oxygen species assay, in addition to the dithiothreitol assay) was comparable during afternoon and nighttime periods, but higher (by at least ∼30%) compared to the morning period, suggesting that SOA formation processes possibly

  13. Design of New Single-phase Multilevel Voltage Source Inverter

    Directory of Open Access Journals (Sweden)

    Rasoul Shalchi Alishah

    2014-07-01

    Full Text Available Multilevel inverters with more number of levels can produce high quality voltage waveforms. In this paper, a new single-phase structure for multilevel voltage source inverter is proposed which can generate a large number of levels with reduced number of IGBTs, gate driver circuits and diodes. Three algorithms for determination of dc voltage sources’ magnitudes are presented which provide odd and even levels at the output voltage waveform. A comparison is presented between proposed multilevel inverter and conventional cascade topology. The proposed topology is analyzed by the experimental and simulation results.

  14. Fabrication of platinum nanoparticles in aqueous solution and solid phase using amphiphilic PB-b-PEO copolymer nanoreactors

    Energy Technology Data Exchange (ETDEWEB)

    Hoda, Numan, E-mail: nhoda@akdeniz.edu.tr [Department of Chemistry, Faculty of Sciences, Akdeniz University, 07058 Antalya (Turkey); Budama, Leyla; Çakır, Burçin Acar; Topel, Önder [Department of Chemistry, Faculty of Sciences, Akdeniz University, 07058 Antalya (Turkey); Ozisik, Rahmi [Department of Materials Science and Engineering and Renssleaer Nanotechnology Center, Rensselaer Polytechnic Institute, Troy, NY 12180 (United States)

    2013-09-01

    Graphical abstract: TEM image of Pt nanoparticles produced by reducing by NaBH{sub 4} within PB-b-PEO micelles in aqueous media (scale bar 1 nm). - Highlights: • Pt nanoparticles were synthesized within amphiphilic diblock copolymer micelles. • The effects of reducing agents and precursor dose on Pt np size were investigated. • The effect on fabrication of Pt np by reducing in aqueous and solid phases was compared. • The size of nanoparticles was about 1.4 nm for all doses and reducing agents types. - Abstract: Fabrication of Pt nanoparticles using an amphiphilic copolymer template in aqueous solution was achieved via polybutadiene-block-polyethyleneoxide copolymer micelles, which acted as nanoreactors. In addition, Pt nanoparticles were synthesized using hydrogen gas as the reducing agent in solid state for the first time to compare against solution synthesis. The influences of loaded precursor salt amount to micelles and the type of reducing agent on the size of nanoparticles were investigated through transmission electron microscopy. It was found that increasing the ratio of precursor salt to copolymer and using different type of reducing agent, even in solid phase reduction, did not affect the nanoparticle size. The average size of Pt nanoparticles was estimated to be 1.4 ± 0.1 nm. The reason for getting same sized nanoparticles was discussed in the light of nucleation, growth process, stabilization and diffusion of nanoparticles within micelles.

  15. Development of a group contribution method to predict aqueous phase hydroxyl radical (HO*) reaction rate constants.

    Science.gov (United States)

    Minakata, Daisuke; Li, Ke; Westerhoff, Paul; Crittenden, John

    2009-08-15

    The hydroxyl radical (HO*) is a strong oxidant that reacts with electron-rich sites of organic compounds and initiates complex chain mechanisms. In order to help understand the reaction mechanisms, a rule-based model was previously developed to predict the reaction pathways. For a kinetic model, there is a need to develop a rate constant estimator that predicts the rate constants for a variety of organic compounds. In this study, a group contribution method (GCM) is developed to predict the aqueous phase HO* rate constants for the following reaction mechanisms: (1) H-atom abstraction, (2) HO* addition to alkenes, (3) HO* addition to aromatic compounds, and (4) HO* interaction with sulfur (S)-, nitrogen (N)-, or phosphorus (P)-atom-containing compounds. The GCM hypothesizes that an observed experimental rate constant for a given organic compound is the combined rate of all elementary reactions involving HO*, which can be estimated using the Arrhenius activation energy, E(a), and temperature. Each E(a) for those elementary reactions can be comprised of two parts: (1) a base part that includes a reactive bond in each reaction mechanism and (2) contributions from its neighboring functional groups. The GCM includes 66 group rate constants and 80 group contribution factors, which characterize each HO* reaction mechanism with steric effects of the chemical structure groups and impacts of the neighboring functional groups, respectively. Literature-reported experimental HO* rate constants for 310 and 124 compounds were used for calibration and prediction, respectively. The genetic algorithms were used to determine the group rate constants and group contribution factors. The group contribution factors for H-atom abstraction and HO* addition to the aromatic compounds were found to linearly correlate with the Taft constants, sigma*, and electrophilic substituent parameters, sigma+, respectively. The best calibrations for 83% (257 rate constants) and predictions for 62% (77

  16. Synthesis and characterization of conditioned carbon with iron nanoparticles for the arsenic removal in aqueous phase

    International Nuclear Information System (INIS)

    Using pineapple husks conditioned with carboxymethylcellulose, hexamine and ferric nitrate, a carbonaceous material was obtained with nanoparticles of Fe (C Fe), which was characterized and tested for arsenic removal in the aqueous phase. The microscopic study showed spheres 4 microns and filaments 100 nm wide, so as iron particles whose diameter decreases to an average of 38.81 nm, when pyrolysis time was increased to 180 min. their distribution in the carbonaceous matrix is homogeneous. According to energy dispersive X-ray spectroscopy, C Fe contains C (82.29%), O (7.23%), K (0.68%), Ca (3.77%) and Fe (6.25%) and its diffraction pattern shows the characteristic peak of Fe (0), which is not observed in the coal without iron. By neutron activation analysis were quantified Al, Br, Ce, Co, Cr, Cs, Eu, Hf, K, Mg, Mn, Na, Rb, Sb, Sc and Zn, they can be involved in the process of sorption of As (v) forming surface active sites. For C Fe and C B characterized by Fourier transform infrared spectrometry, groups C-H, C=O, C=C, -Nh, NH2, isocyanate and isonitrile were found, the last two were formed by the present hexamine. X-ray photoelectron spectroscopy showed energy states of C 1 and O 1 in pineapple shell washed, shell conditioned with iron, C Fe at different times and the pyrolysis coal without iron (C B). The material C Fe 180 presented a specific area of 167 m2/g and 7.12 ± 1 sites/nm2 isoelectric point while pHi = 11.1 C B is 98.80 m2/g specific area and 1.5 ± 1 sites/nm2 and pHi = 10.6, being favorable to the sorption process. The highest removal of As(v) for both materials was at ph = 2, fitting the kinetic data to pseudo-second order model. The isotherms as a function of concentration were adjusted to Freundlich model indicating multilayer chemisorption at specific sites of a heterogeneous medium. Characterization by scanning electron microscopy after the sample sorption Fe nanoparticles remain in the carbonaceous matrix being not affected by the agitation of

  17. Aqueous-phase photochemical oxidation and direct photolysis of vanillin - a model compound of methoxy-phenols from biomass burning

    Science.gov (United States)

    Li, Y. J.; Huang, D. D.; Cheung, H. Y.; Lee, A. K. Y.; Chan, C. K.

    2013-10-01

    We present here experimental results on aqueous-phase (A) photochemical oxidation (with UV and OH radicals generated from H2O2 photolysis) and (B) direct photolysis (with only UV irradiation) of a methoxy-phenol, vanillin (VL), as a model compound from biomass burning. Both on-line aerosol mass spectrometric (AMS) characterization and off-line chemical analyses were performed. AMS analyses of dried atomized droplets of the bulk reacting mixtures showed that VL almost entirely evaporates during the drying process. Large amounts of organic mass remained in the particle phase after reactions under both conditions. Under condition (A), AMS measured organic mass first increased rapidly and then decreased, attributable to the formation of non-volatile products and subsequent formation of smaller and volatile products, respectively. The oxygen-to-carbon (O:C) ratio of the products reached 1.5 after about 80 min, but dropped substantially thereafter. In contrast, organic mass increased slowly under condition (B). The O:C ratio reached 1.0 after 180 min. In off-line analyses, small oxygenates were detected under condition (A), while hydroxylated products and dimers of VL were detected under condition (B). Particle hygroscopic growth factor (GF) and cloud condensation nuclei (CCN) activity of the reacting mixtures were found to be dependent on both organic volume fraction and the degree of oxygenation of organics. Results show that (1) aqueous-phase processes can lead to the retention of a large portion of the organic mass in the particle phase; (2) once retained, this portion of organic mass significantly changes the hygroscopicity and CCN activity of the aerosol particles; (3) intensive photochemical oxidation gave rise to an O:C ratio as high as 1.5 but the ratio decreased as further oxidation led to smaller and more volatile products; and (4) polymerization occurred with direct photolysis, resulting in high-molecular-weight products of a yellowish color. This study

  18. Aqueous-phase photochemical oxidation and direct photolysis of vanillin - a model compound of methoxy phenols from biomass burning

    Science.gov (United States)

    Li, Y. J.; Huang, D. D.; Cheung, H. Y.; Lee, A. K. Y.; Chan, C. K.

    2014-03-01

    We present here experimental results on aqueous-phase (A) photochemical oxidation (with UV and OH radicals generated from H2O2 photolysis) and (B) direct photolysis (with only UV irradiation) of a methoxy phenol, vanillin (VL), as a model compound from biomass burning. Both on-line aerosol mass spectrometric (AMS) characterization and off-line chemical analyses were performed. AMS analyses of dried atomized droplets of the bulk reacting mixtures showed that VL almost entirely evaporates during the drying process. Large amounts of organic mass remained in the particle phase after reactions under both conditions. Under condition (A), AMS measured organic mass first increased rapidly and then decreased, attributable to the formation of non-volatile products and subsequent formation of smaller and volatile products, respectively. The oxygen-to-carbon (O : C) ratio of the products reached 1.5 after about 80 min, but dropped substantially thereafter. In contrast, organic mass increased slowly under condition (B). The O : C ratio reached 1.0 after 180 min. In off-line analyses, small oxygenates were detected under condition (A), while hydroxylated products and dimers of VL were detected under condition (B). Particle hygroscopic growth factor (GF) and cloud condensation nuclei (CCN) activity of the reacting mixtures were found to depend on both organic volume fraction and the degree of oxygenation of organics. Results show that (1) aqueous-phase processes can lead to the retention of a large portion of the organic mass in the particle phase; (2) once retained, this portion of organic mass significantly changes the hygroscopicity and CCN activity of the aerosol particles; (3) intensive photochemical oxidation gave rise to an O : C ratio as high as 1.5 but the ratio decreased as further oxidation led to smaller and more volatile products; and (4) polymerization occurred with direct photolysis, resulting in high-molecular-weight products of a yellowish color. This study

  19. 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...

  20. 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

  1. An alternative method to isolate protease and phospholipase A2 toxins from snake venoms based on partitioning of aqueous two-phase systems

    Directory of Open Access Journals (Sweden)

    GN Gómez

    2012-01-01

    Full Text Available Snake venoms are rich sources of active proteins that have been employed in the diagnosis and treatment of health disorders and antivenom therapy. Developing countries demand fast economical downstream processes for the purification of this biomolecule type without requiring sophisticated equipment. We developed an alternative, simple and easy to scale-up method, able to purify simultaneously protease and phospholipase A2 toxins from Bothrops alternatus venom. It comprises a multiple-step partition procedure with polyethylene-glycol/phosphate aqueous two-phase systems followed by a gel filtration chromatographic step. Two single bands in SDS-polyacrylamide gel electrophoresis and increased proteolytic and phospholipase A2 specific activities evidence the homogeneity of the isolated proteins.

  2. Conformation of lanthanides complexes of L-serine phosphate and ethanolamine phosphate in aqueous phase

    International Nuclear Information System (INIS)

    NMR paramagnetic shifts induced by rare earth cations lead to conformations of complexes in aqueous solution. A computer treatment is developped for complexes of L-serine phosphate and ethanolamine phosphate with lanthanides in acidic solution (pH=1 to 1.8). Angle and distance values are discussed with a hindered rotation about P-O1 bond

  3. Phosphate removal from aqueous phase using iron impregnated natural clay: kinetic and equilibrium modeling

    International Nuclear Information System (INIS)

    Even through phosphate is a major nutrient for plants and microorganisms, its excess amount (>1 ng/L) is often responsible for eutrophication of water bodies. Eutrophication is a phenomenon of algal booming causing high economic damage due to the death of tones of fishes. Therefore, nowadays, the removal of phosphate from aqueous solution and municipal sewage attains great concern. (Author)

  4. Aqueous phase reforming of ethylene glycol - Role of intermediates in catalyst performance

    NARCIS (Netherlands)

    Vlieger, de D.J.M.; Mojet, B.L.; Lefferts, L.; Seshan, K.

    2012-01-01

    Liquid product formation during the aqueous catalytic reforming of ethylene glycol (EG) was studied up to 450 °C and 250 bar pressure. Methanol, ethanol, and acetic acid were the main liquid by-products during EG reforming in the presence of alumina-supported Pt and Pt–Ni catalysts. The effect of th

  5. Flocculation performance of a cationic biopolymer derived from a cellulosic source in mild aqueous solution.

    Science.gov (United States)

    Liimatainen, Henrikki; Sirviö, Juho; Sundman, Ola; Visanko, Miikka; Hormi, Osmo; Niinimäki, Jouko

    2011-10-01

    The flocculation behavior of cationic, quaternary ammonium groups containing cellulosic biopolymers, CDACs, synthesized by cationizing dialdehyde cellulose in mild aqueous solution was studied in a kaolin suspension. In particular, the role of CDAC dosage and solution pH, NaCl concentration, and temperature were clarified. In addition, the initial apparent charge densities (CDs), particle sizes, ζ-potential, and stability of CDs were determined. CDACs possessed a high flocculation activity in neutral and acidic solutions, but a significant decrease was observed in alkaline solutions (pH >9). This was also seen as a decline in the apparent CD and particle size of the CDACs in alkaline conditions. The measurements also indicated that the apparent CD decreased to a constant level of 3 mmol/g in aqueous solutions. However, no notable decrease in flocculation performance was obtained after several days of storage. Moreover, the variation of NaCl concentration and temperature did not affect the flocculation activity. PMID:21862324

  6. ANALYSIS OF SULFONATES IN AQUEOUS SAMPLES BY ION-PAIR LC/ESI-MS/MS WITH IN-SOURCE CID FOR ADDUCT PEAK ELIMINATION

    Energy Technology Data Exchange (ETDEWEB)

    OUYANG,S.; VAIRAVAMURTHY,M.A.

    1999-06-13

    Determination of low-molecular-weight organic sulfonates (e.g. taurine and cysteic acid) in aqueous solutions is important in many applications of biological, environmental and pharmaceutical sciences. These compounds are difficult to be determined by commonly used reversed-phase liquid chromatographic separation combined with UV-Visible detection because of their high solubility and the lack chromophoric moieties. Here the authors report a method combining ion-pair liquid chromatography and electrospray ionization tandem mass spectrometry (IPLC/ESI-MS/MS)for determining sulfonates. The ability of low-molecular-weight sulfonates to form ion-pairs with quaternary ammonium cations in aqueous solutions allowed LC separation with a C{sub 18} column. Detection of the sulfonates was accomplished with ESI-MS that lends a universal mode of mass detection for polar, water soluble compounds. An in-source collision induced dissociation (CID) was applied to eliminate the adduct peaks in mass spectra. Characteristic marker ions showed in the second stage mass spectra lent a method for identifying sulfonates.

  7. NUMERICAL STUDY OF NON-AQUEOUS PHASE LIQUID TRANSPORT IN A SINGLE FILLED FRACTURE BY LATTICE BOLTZMANN METHOD

    Institute of Scientific and Technical Information of China (English)

    DOU Zhi; ZHOU Zhi-fang; HUANG Yong; WU Wei

    2012-01-01

    In this article,the Non-Aqueous Phase Liquid (NAPL) transport in the single filled fracture was studied with the Shan-Chen multi-component multiphase Lattice Boltzmann Method (LBM) with special consideration of wettability effects.With the help of the model,the contact angle of the non-wetting phase and wetting phase interface at a solid wall could be adjusted.By considering a set of appropriate boundary conditions,the fractured conductivity was investigated in condition that the NAPL blocks the channels in the single filled fracture.In order to study the wettability effects on the NAPL transport,a constant driving force was introduced in the Shan-Chen multi-component multiphase LBM.Flow regimes with different wettabilities were discussed.Simulated results show that the LBM is a very instrumental method for simulating and studying the immiscible multiphase flow problems in single filled fracture.

  8. The redox chemistry of neptunium in γ-irradiated aqueous nitric acid in the presence of an organic phase

    International Nuclear Information System (INIS)

    The radiolytic changes in oxidation state for solutions of initially Np(V) and/or Np(VI) were investigated by gamma-irradiation in conjunction with UV/Vis spectroscopy of the aqueous phase. Samples were irradiated in varying concentrations of nitric acid, and with or without the presence of 30 % TBP in dodecane. At short irradiation times Np(V) was oxidized to Np(VI), even in the presence of the organic phase. Upon the radiolytic production of sufficient amounts of nitrous acid, reduction of Np(VI) to Np(V) occurred in both phases. This was accompanied by stripping of the previously extracted Np(VI). Nitric acid concentrations of 6 M mitigated this reduction. (author)

  9. Can affinity interactions influence the partitioning of glucose-6-phosphate dehydrogenase in two-phase aqueous micellar systems?

    Directory of Open Access Journals (Sweden)

    André M. Lopes

    2008-01-01

    Full Text Available In this work, we provide an investigation of the role and strength of affinity interactions on the partitioning of the glucose-6-phosphate dehydrogenase in aqueous two-phase micellar systems. These systems are constituted of micellar surfactant solutions and offer both hydrophobic and hydrophilic environments, providing selectivity to biomolecules. We studied G6PD partitioning in systems composed of the nonionic surfactants, separately, in the presence and absence of affinity ligands. We observed that G6PD partitions to the micelle-poor phase, owing to the strength of excluded-volume interactions in these systems that drive the protein to the micelle-poor phase, where there is more free volume available.

  10. Linear free energy relationships between aqueous phase hydroxyl radical reaction rate constants and free energy of activation.

    Science.gov (United States)

    Minakata, Daisuke; Crittenden, John

    2011-04-15

    The hydroxyl radical (HO(•)) is a strong oxidant that reacts with electron-rich sites on organic compounds and initiates complex radical chain reactions in aqueous phase advanced oxidation processes (AOPs). Computer based kinetic modeling requires a reaction pathway generator and predictions of associated reaction rate constants. Previously, we reported a reaction pathway generator that can enumerate the most important elementary reactions for aliphatic compounds. For the reaction rate constant predictor, we develop linear free energy relationships (LFERs) between aqueous phase literature-reported HO(•) reaction rate constants and theoretically calculated free energies of activation for H-atom abstraction from a C-H bond and HO(•) addition to alkenes. The theoretical method uses ab initio quantum mechanical calculations, Gaussian 1-3, for gas phase reactions and a solvation method, COSMO-RS theory, to estimate the impact of water. Theoretically calculated free energies of activation are found to be within approximately ±3 kcal/mol of experimental values. Considering errors that arise from quantum mechanical calculations and experiments, this should be within the acceptable errors. The established LFERs are used to predict the HO(•) reaction rate constants within a factor of 5 from the experimental values. This approach may be applied to other reaction mechanisms to establish a library of rate constant predictions for kinetic modeling of AOPs. PMID:21410278

  11. 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.

  12. Phase and Frequency Locked Magnetrons for SRF Sources

    Energy Technology Data Exchange (ETDEWEB)

    Neubauer, Michael [Muons, Inc.; Johnson, Rolland

    2014-09-12

    There is great potential for a magnetron power source that can be controlled both in phase and frequency. Such a power source could revolutionize many particle accelerator systems that require lower capital cost and/or higher power efficiency. Beyond the accelerator community, phase and frequency locked magnetons could improve radar systems around the world and make affordable phased arrays for wireless power transmission for solar powered satellites. This joint project of Muons, Inc., Fermilab, and L-3 CTL was supported by an STTR grant monitored by the Nuclear Physics Office of the DOE Office of Science. The object of the program was to incorporate ferrite materials into the anode of a magnetron and, with appropriate biasing of the ferrites, to maintain frequency lock and to allow for frequency adjustment of the magnetron without mechanical tuners. If successful, this device would have a dual use both as a source for SRF linacs and for military applications where fast tuning of the frequency is a requirement. In order to place the materials in the proper location, several attributes needed to be modeled. First the impact of the magnetron’s magnetic field needed to be shielded from the ferrites so that they were not saturated. And second, the magnetic field required to change the frequency of the magnetron at the ferrites needed to be shielded from the region containing the circulating electrons. ANSYS calculations of the magnetic field were used to optimize both of these parameters. Once the design for these elements was concluded, parts were fabricated and a complete test assembly built to confirm the predictions of the computer models. The ferrite material was also tested to determine its compatibility with magnetron tube processing temperatures. This required a vacuum bake out of the chosen material to determine the cleanliness of the material in terms of outgassing characteristics, and a subsequent room temperature test to verify that the characteristics of

  13. Propeller-Like Nanorod-Upconversion Nanoparticle Assemblies with Intense Chiroptical Activity and Luminescence Enhancement in Aqueous Phase.

    Science.gov (United States)

    Wu, Xiaoling; Xu, Liguang; Ma, Wei; Liu, Liqiang; Kuang, Hua; Kotov, Nicholas A; Xu, Chuanlai

    2016-07-01

    Propeller-like nanoscale assemblies with exceptionally intense chiroptical activity and strong luminescence are prepared using gold nanorods and upconversion nanoparticles. The circular dichroism intensity of the tetramer reached 80.9 mdeg, with g-factor value of 2.1 × 10(-2) . The enhancement factor of upconversion luminescence is as high as 21.3 in aqueous phase. Attomolar bioanalysis of a cancer biomarker with two model is also achieved, showing potential for early disease diagnosis and environmental monitoring. PMID:27158947

  14. Aqueous two-phase flotation for primary recovery of bacteriocin-like inhibitory substance (BLIS) from Pediococcus acidilactici Kp10.

    Science.gov (United States)

    Md Sidek, Nurul Lyana; Tan, Joo Shun; Abbasiliasi, Sahar; Wong, Fadzlie Wong Faizal; Mustafa, Shuhaimi; Ariff, Arbakariya B

    2016-08-01

    An aqueous two-phase flotation (ATPF) system based on polyethylene glycol (PEG) and sodium citrate (NaNO3C6H5O7·2H2O) was considered for primary recovery of bacteriocin-like inhibitory substance (BLIS) from Pediococcus acidilactici Kp10. The effects of ATPF parameters namely phase composition, tie-line length (TLL), volume ratio between the two phases (VR), amount of crude load (CL), pH, nitrogen gas flow rate (FR) and flotation time (FT) on the performance of recovery were evaluated. BLIS was mainly concentrated into the upper PEG-rich phase in all systems tested so far. The optimum conditions for BLIS purification, which composed of PEG 8000/sodium citrate, were: TLL of 42.6, VR of 0.4, CL of 22% (w/w), pH 7, average FT of 30min and FR of 20mL/min. BLIS was partially purified up to 5.9-fold with a separation efficiency of 99% under this optimal conditions. A maximum yield of BLIS activity of about 70.3% was recovered in the PEG phase. The BLIS from the top phase was successfully recovered with a single band in SDS-gel with molecular weight of about 10-15kDa. ATPF was found to be an effective technique for the recovery of BLIS from the fermentation broth of P. acidilactici Kp10. PMID:27262666

  15. The protein-water phase diagram and the growth of protein crystals from aqueous solution

    NARCIS (Netherlands)

    Haas, C; Drenth, J

    1998-01-01

    The phase diagram of a protein-water system is described with a simple model with parameters for the interaction between protein molecules in the liquid and in the solid phase. The model reproduces essential features of the phase diagram, such as the (metastable) liquid-liquid immiscibility region a

  16. Ca(2+) -complex stability of GAPAGPLIVPY peptide in gas and aqueous phase, investigated by affinity capillary electrophoresis and molecular dynamics simulations and compared to mass spectrometric results.

    Science.gov (United States)

    Nachbar, Markus; El Deeb, Sami; Mozafari, Mona; Alhazmi, Hassan A; Preu, Lutz; Redweik, Sabine; Lehmann, Wolf Dieter; Wätzig, Hermann

    2016-03-01

    Strong, sequence-specific gas-phase bindings between proline-rich peptides and alkaline earth metal ions in nanoESI-MS experiments were reported by Lehmann et al. (Rapid Commun. Mass Spectrom. 2006, 20, 2404-2410), however its relevance for physiological-like aqueous phase is uncertain. Therefore, the complexes should also be studied in aqueous solution and the relevance of the MS method for binding studies be evaluated. A mobility shift ACE method was used for determining the binding between the small peptide GAPAGPLIVPY and various metal ions in aqueous solution. The findings were compared to the MS results and further explained using computational methods. While the MS data showed a strong alkaline earth ion binding, the ACE results showed nonsignificant binding. The proposed vacuum state complex also decomposed during a molecular dynamic simulation in aqueous solution. This study shows that the formed stable peptide-metal ion adducts in the gas phase by ESI-MS does not imply the existence of analogous adducts in the aqueous phase. Comparing peptide-metal ion interaction under the gaseous MS and aqueous ACE conditions showed huge difference in binding behavior.

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

    Energy Technology Data Exchange (ETDEWEB)

    Damrongsiri, S. [Center of Excellence on Hazardous Substance Management (HSM), Chulalongkorn University, Phaya-Thai Rd., Bangkok (Thailand); Tongcumpou, C., E-mail: tchantra@chula.ac.th [Center of Excellence on Hazardous Substance Management (HSM), Chulalongkorn University, Phaya-Thai Rd., Bangkok (Thailand); Environmental Research Institute, Chulalongkorn University (Thailand); Sabatini, D.A. [School of Civil Engineering and Environmental Science, The University of Oklahoma, Oklahoma (United States)

    2013-03-15

    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.

  18. Processes controlling the migration and biodegradation of Non-aqueous phase liquids (NAPLs) within fractured rocks in the vadose zone FY97 annual report

    Energy Technology Data Exchange (ETDEWEB)

    Geller, J.T.; Holman, Hoi-Ying; Conrad, M. [and others

    1998-02-01

    Subsurface contamination from volatile organic compounds (VOCs) has been found at many Department of Energy (DOE), Department of Defense (DoD) and industrial sites due to the widespread use of organic solvents and hydrocarbon fuels. At ambient pressures and temperatures in the shallow subsurface, these substances are liquids that are immiscible with water; hence they are commonly designated as non-aqueous phase liquids (NAPLs). At some DOE sites, NAPLs are the presumed source of groundwater contamination in fractured rocks, such as basalts (at Hanford and Idaho National Engineering and Environmental Laboratory (INEEL)), shales (Oak Ridge Y-12 Plant), and welded tuffs (Los Alamos National Laboratory (LANL)). The flow, transport and biodegradation processes controlling NAPL behavior in the vadose zone must be understood in order to establish the possible extent of contamination, the risk to groundwater supplies, and appropriate remediation action. This is particularly important in and sites with deep water tables (such as at Hanford, INEEL and LANL). In fractured rock aquifers, NAPL migration is likely to be dominated by the highly permeable pathways provided by rock fractures and joints. Two- and three-phase fluid phases may be present in vadose zone fractures, including NAPL-gas, NAPL-water (in regions of perched water) and NAPL-water-gas.

  19. 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

  20. Measurement and Correlation of Partition Coefficients of Baicalin in EOPO/Salt Aqueous Two-Phase Systems

    Institute of Scientific and Technical Information of China (English)

    李伟; 朱自强

    2002-01-01

    The partition coefficients of baicalin were measured in ethylene oxide and propylene oxide(EOPO)/salt aqueous two-phase systems at 298.15K,It was found that most of baicalin partitioned into EOPO-rich phase.The partition coefficients of baicalin varied from 10 to 120.The effect of various factors,including tie-line lngth,salt composition,molecular weight of EOPO,and solution pH,on the partition behavior was investigated on EOPO/salt systems.Furthermore the partition coefficients of baicalin were correlated using the modified Diamond-Hsu model.Good agreement with experimental data is obtained.The average relative deviations are less than 5.0%.

  1. Morphological and phase evolution of TiO 2 nanocrystals prepared from peroxotitanate complex aqueous solution: Influence of acetic acid

    Science.gov (United States)

    Chang, Jeong Ah; Vithal, Muga; Baek, In Chan; Seok, Sang Il

    2009-04-01

    Nanosized anatase and rutile TiO 2 having different shape, phase and size have been prepared from aqueous solutions of peroxo titanium complex starting from titanium(IV) isopropoxide (TTIP), acetic acid and hydrogen peroxide (H 2O 2) in water/isopropanol media by a facile sol-gel process. The TiO 2 nanocrystals are characterized by powder X-ray diffraction (XRD), Raman spectroscopy, FT-IR spectroscopy, TEM, high resolution transmission electron microscopy (HRTEM) and selected area electron diffraction (SAED) techniques. The influence of pH and the sequence of addition of reaction contents on the phase and morphology of TiO 2 are studied. The reasons for the observation of only anatase and/or mixture of anatase and rutile are given.

  2. Theoretical study of phase behaviour of DLVO model for lysozyme and γ-crystalline aqueous electrolyte solutions

    Directory of Open Access Journals (Sweden)

    R. Melnyk

    2015-03-01

    Full Text Available Mean spherical approximation (MSA, second-order Barker-Henderson (BH perturbation theory and thermodynamic perturbation theory (TPT for associating fluids in combination with BH perturbation theory are applied to the study of the structural properties and phase behaviour of the Derjaguin-Landau-Verwey-Overbeek (DLVO model of lysozyme and γ-cristalline aqueous electrolyte solutions. Predictions of the MSA for the structure factors are in good agreement with the corresponding computer simulation predictions. The agreement between theoretical results for the liquid-gas phase diagram and the corresponding results of the experiment and computer simulation is less satisfactory, with predictions of the combined BH-TPT approach being the most accurate.

  3. Impact of polymers on the crystallization and phase transition kinetics of amorphous nifedipine during dissolution in aqueous media.

    Science.gov (United States)

    Raina, Shweta A; Alonzo, David E; Zhang, Geoff G Z; Gao, Yi; Taylor, Lynne S

    2014-10-01

    The commercial and clinical success of amorphous solid dispersions (ASD) in overcoming the low bioavailability of poorly soluble molecules has generated momentum among pharmaceutical scientists to advance the fundamental understanding of these complex systems. A major limitation of these formulations stems from the propensity of amorphous solids to crystallize upon exposure to aqueous media. This study was specifically focused on developing analytical techniques to evaluate the impact of polymers on the crystallization behavior during dissolution, which is critical in designing effective amorphous formulations. In the study, the crystallization and polymorphic conversions of a model compound, nifedipine, were explored in the absence and presence of polyvinylpyrrolidone (PVP), hydroxypropylmethyl cellulose (HPMC), and HPMC-acetate succinate (HPMC-AS). A combination of analytical approaches including Raman spectroscopy, polarized light microscopy, and chemometric techniques such as multivariate curve resolution (MCR) were used to evaluate the kinetics of crystallization and polymorphic transitions as well as to identify the primary route of crystallization, i.e., whether crystallization took place in the dissolving solid matrix or from the supersaturated solutions generated during dissolution. Pure amorphous nifedipine, when exposed to aqueous media, was found to crystallize rapidly from the amorphous matrix, even when polymers were present in the dissolution medium. Matrix crystallization was avoided when amorphous solid dispersions were prepared, however, crystallization from the solution phase was rapid. MCR was found to be an excellent data processing technique to deconvolute the complex phase transition behavior of nifedipine.

  4. Passage of TBP-uranyl complexes from aqueous-organic interface to the organic phase: insights from molecular dynamics simulation.

    Science.gov (United States)

    Sahu, Pooja; Ali, Sk Musharaf; Shenoy, Kalasanka Trivikram

    2016-08-24

    The present study reports molecular dynamics simulations for biphasic systems comprising tributyl phosphate (TBP) in dodecane and uranyl nitrate in the aqueous phase, which are key chemical species in the well-known Pu-U extraction (PUREX) process. An attempt has been made to understand the nature of interface and mechanism of 'TBP associated uranyl' crossing under neutral and acidic conditions. Results show that the solvent density undergoes large fluctuation near the interface depending on the nature of the aqueous-organic phase. The study provides compelling evidence of experimentally observed reorganization of interfacial complexes at the interface and their structural reformation during extraction. It has been observed that the surface active nature of TBP and their interfacial coverage is modulated by the nature of incorporated solute species and their location with respect to the interface. Also, the TBP structuring near the interface is destroyed when an acidic interface is considered rather than a neutral one which favors the uranyl extraction. With an acidic interface, the water humidity of organic phase was observed to be increased in the experiments. Furthermore, the acid/water solubility in the organic phase was observed to be influenced by selection of acid models and their concentration. Simulations with high acid concentration show water pocket formation in the organic phase. However, in the case of dissociated ions or a mixture of both, no such water pool is observed and the extracted water remains dispersed in the organic phase, having the tendency to be replaced by HNO3 because of preferred TBP·HNO3 complexation over TBP·H2O. Most remarkably, the present study makes evident the TBP-induced charge redistribution of uranyl complexes during migration from the interface to the bulk organic phase, which contributes to drive uranyl complexes such as UO2·NO3·4TBP, UO2·5TBP and UO2·NO3·3TBP·HNO3 in the organic phase, and this was reestablished by

  5. Effect of biochar addition on hydrogen and methane production in two-phase anaerobic digestion of aqueous carbohydrates food waste.

    Science.gov (United States)

    Sunyoto, Nimas M S; Zhu, Mingming; Zhang, Zhezi; Zhang, Dongke

    2016-11-01

    Effect of biochar addition on hydrogen and methane production in two-phase anaerobic digestion of aqueous carbohydrates was studied using bench-scale bioreactors. The cultures with biochar additions were placed in 100ml reactors and incubated at 35°C and pH 5 for hydrogen production. The residual cultures were then used for methane production, incubated at 35°C and pH 7. Daily yields of hydrogen and methane and weekly yield of volatile fatty acids (VFA) were measured. The hydrogen and methane production potentials, rate and lag phases of the two phases were analysed using the Gompertz model. The results showed that biochar addition increased the maximum production rates of hydrogen by 32.5% and methane 41.6%, improved hydrogen yield by 31.0% and methane 10.0%, and shortened the lag phases in the two phases by 36.0% and 41.0%, respectively. Biochar addition also enhanced VFA generation during hydrogen production and VFA degradation in methane production.

  6. Effect of biochar addition on hydrogen and methane production in two-phase anaerobic digestion of aqueous carbohydrates food waste.

    Science.gov (United States)

    Sunyoto, Nimas M S; Zhu, Mingming; Zhang, Zhezi; Zhang, Dongke

    2016-11-01

    Effect of biochar addition on hydrogen and methane production in two-phase anaerobic digestion of aqueous carbohydrates was studied using bench-scale bioreactors. The cultures with biochar additions were placed in 100ml reactors and incubated at 35°C and pH 5 for hydrogen production. The residual cultures were then used for methane production, incubated at 35°C and pH 7. Daily yields of hydrogen and methane and weekly yield of volatile fatty acids (VFA) were measured. The hydrogen and methane production potentials, rate and lag phases of the two phases were analysed using the Gompertz model. The results showed that biochar addition increased the maximum production rates of hydrogen by 32.5% and methane 41.6%, improved hydrogen yield by 31.0% and methane 10.0%, and shortened the lag phases in the two phases by 36.0% and 41.0%, respectively. Biochar addition also enhanced VFA generation during hydrogen production and VFA degradation in methane production. PMID:27474855

  7. Derivatisation/solid-phase microextraction followed by gas chromatography-mass spectrometry for the analysis of phenoxy acid herbicides in aqueous samples

    DEFF Research Database (Denmark)

    Nilsson, Torben; Baglio, Daniela; Galdo-Miguez, Isabel;

    1998-01-01

    Different combinations of derivatisation and solid-phase microextraction followed by gas chromatography-mass spectrometry were optimised and evaluated for the analysis of phenoxy acid herbicides in water. The most successful derivatisation approach was aqueous-phase derivatisation with benzyl...

  8. 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%.

  9. Entropy-enthalpy Compensation of Biomolecular Systems in Aqueous Phase: a Dry Perspective.

    Science.gov (United States)

    Movileanu, Liviu; Schiff, Eric A

    2013-01-01

    We survey thermodynamic measurements on processes involving biological macromolecules in aqueous solution, which illustrate well the ubiquitous phenomenon of entropy-enthalpy compensation. The processes include protein folding/unfolding and ligand binding/unbinding, with compensation temperatures varying by about 50 K around an average near 293 K. We show that incorporating both near-exact entropy-enthalpy compensation (due to solvent relaxation) and multi-excitation entropy (from vibrational quanta) leads to a compensation temperature in water of about 230 K. We illustrate a general procedure for subtracting solvent and environment-related terms to determine the bare Gibbs free energy changes of chemical processes.

  10. Stripping of TBP degraded product along with actinides from organic phase generated during the remediation of the aqueous phase of spent organic waste storage tank

    International Nuclear Information System (INIS)

    Degraded products of Tri butyl phosphate (TBP) are generated during extraction of U and Pu by PUREX due to high radiation field. Sodium carbonate wash is given to clean up the TBP solvent and the wash liquid is in a separate tank along with the spent organic waste. Though the aqueous phase from this tank comes intermediate level liquid waste category, presence of the degrade products of TBP are creating problem during its treatment by ion exchange process. To remediate this waste for ion exchange treatment, the degraded products of TBP are removed by solvent extraction using spent TBP stored in the same tank as solvent. Present paper details the stripping of the TBP degraded product along with alpha activity from the organic phase

  11. Temperature- and pH-dependent aqueous-phase kinetics of the reactions of glyoxal and methylglyoxal with atmospheric amines and ammonium sulfate

    Science.gov (United States)

    Sedehi, Nahzaneen; Takano, Hiromi; Blasic, Vanessa A.; Sullivan, Kristin A.; De Haan, David O.

    2013-10-01

    Reactions of glyoxal (Glx) and methylglyoxal (MG) with primary amines and ammonium salts may produce brown carbon and N-containing oligomers in aqueous aerosol. 1H NMR monitoring of reactant losses and product appearance in bulk aqueous reactions were used to derive rate constants and quantify competing reaction pathways as a function of pH and temperature. Glx + ammonium sulfate (AS) and amine reactions generate products containing C-N bonds, with rates depending directly on pH: rate = (70 ± 60) M-1 s-1fAld [Glx]totfAm [Am]tot, where fAld is the fraction of aldehyde with a dehydrated aldehyde functional group, and fAm is the fraction of amine or ammonia that is deprotonated at a given pH. MG + amine reactions generate mostly aldol condensation products and exhibit less pH dependence: rate = 10[(0.36 ± 0.06) × pH - (3.6 ± 0.3)] M-1 s-1fAld [MG]tot [Am]tot. Aldehyde + AS reactions are less temperature-dependent (Ea = 18 ± 8 kJ mol-1) than corresponding amine reactions (Ea = 50 ± 11 kJ mol-1). Using aerosol concentrations of [OH] = 10-12 M, [amine]tot = [AS] = 0.1 M, fGlx = 0.046 and fMG = 0.09, we estimate that OH radical reactions are normally the major aerosol-phase sink for both dicarbonyl compounds. However, reactions with AS and amines together can account for up to 12 and 45% of daytime aerosol-phase glyoxal and methylglyoxal reactivity, respectively, in marine aerosol at pH 5.5. Reactions with AS and amines become less important in acidic or non-marine aerosol, but may still be significant atmospheric sources of brown carbon, imidazoles, and nitrogen-containing oligomers.

  12. Aqueous phase oligomerization of α,β-unsaturated carbonyls and acids investigated using ion mobility spectrometry coupled to mass spectrometry (IMS-MS)

    Science.gov (United States)

    Renard, Pascal; Tlili, Sabrine; Ravier, Sylvain; Quivet, Etienne; Monod, Anne

    2016-04-01

    One of the current essential issues to unravel our ability to forecast future climate change and air quality, implies a better understanding of natural processes leading to secondary organic aerosol (SOA) formation, and in particular the formation and fate of oligomers. The difficulty in characterizing macromolecules is to discern between large oxygenated molecules from series of oligomers containing repeated small monomers of diverse structures. In the present study, taking advantage from previously established radical vinyl oligomerization of methyl vinylketone (MVK) in the aqueous phase, where relatively simple oligomers containing up to 14 monomers were observed, we have investigated the same reactivity on several other unsaturated water soluble organic compounds (UWSOCs) and on a few mixtures of these precursor compounds. The technique used to characterize the formed oligomers was a traveling wave ion mobility spectrometry coupled to a hybrid quadrupole - time of flight mass spectrometer (IMS-MS) fitted with an electrospray source and ultra-high performance liquid chromatography (UPLC). The technique allows for an additional separation, especially for large ions, containing long carbon chains. We have shown the efficiency of the IMS-mass spectrometry technique to detect oligomers derived from MVK photooxidation in the aqueous phase. The results were then compared to other oligomers, derived from ten other individual biogenic UWSOCs. The technique allowed distinguishing between different oligomers arising from different precursors. It also clearly showed that compounds bearing a non-conjugated unsaturation did not provide oligomerization. Finally, it was shown that the IMS-mass spectrometry technique, applied to mixtures of unsaturated conjugated precursors, exhibited the ability of these precursors to co-oligomerize, i.e. forming only one complex oligomer system bearing monomers of different structures. The results are discussed in terms of atmospheric

  13. Potential pollutant sources in a Choptank River subwatershed: Influence of agricultural and residential land use and aqueous and atmospheric sources

    Science.gov (United States)

    Agriculture and animal feeding operations have been implicated as sources of water pollution along the Choptank River, an estuary and tributary of the Chesapeake Bay. This study examined a subwatershed within the Choptank River watershed for effects of land use on water quality. Water and sediment...

  14. Insights into Aqueous-phase processing through Comparison of the Organic Chemical Composition of Atmospheric Particles and Cloud Water in the Southeast United States

    Science.gov (United States)

    Boone, E.; Laskin, J.; Laskin, A.; Wirth, C.; Shepson, P. B.; Stirm, B. H.; Pratt, K.

    2014-12-01

    Organic compounds comprise a significant mass fraction of submicron atmospheric particles with considerable contribution from secondary organic aerosol (SOA), a large fraction of which is formed from the oxidation of biogenic volatile organic compounds. Aqueous-phase reactions in particles and cloud droplets are suggested to increase SOA mass and change the chemical composition the particles following cloud evaporation. Aqueous-phase processing may also explain discrepancies between measurements and models. To gain a better understanding of these processes, cloud water and below-cloud atmospheric particles were collected onboard a research aircraft during the Southeast Oxidants and Aerosol Study (SOAS) over Alabama in June 2013. Nanospray desorption electrospray ionization (nano-DESI) and direct electrospray ionization (ESI) coupled with high resolution mass spectrometry were utilized to compare the organic molecular composition of the particle and cloud water samples, respectively. Several hundred unique compounds have been identified in the particle and cloud water samples, allowing possible aqueous-phase reactions to be examined. Hydrolysis of organosulfate compounds, aqueous-phase formation of nitrogen-containing compounds, and possible fragmentation of oligomeric compounds will be discussed, with comparisons to previous laboratory studies. This study provides insights into aqueous-phase reactions in ambient cloud droplets.

  15. Aqueous Phase Non Enzymatic Chemistry of Cyanide, Formaldehyde and RNH2

    Science.gov (United States)

    Lerner, Narcinda R.; Chang, Sherwood (Technical Monitor)

    1994-01-01

    It is postulated that amino acids were produced on the early earth from dilute aqueous solution of cyanide, carbonyls and ammonia (the Strecker synthesis RNH2 + R"R""C=O + KCN yields H-N(R)-C(R")(R"")-CO2H. We have studied the products obtained from dilute aqueous solutions of cyanide, formaldehyde (R"=R""=H), ammonia (R=H) and amino acids. Solutions in the pH range from 8 to 10. at room temperature and at reactant concentrations from 0.001 M to 0.3 M have been studied. With R= H product yields were low (less than 3%). Only with R"=R""=H and R represented by the following: CH2CO2H (glycine); CH(CH3)CO2H (alanine); CH(CH2CH3)CO2H (a-amino n=butyric acids); C(CH3)2(CO2H) (a-aminoisobutyric acid); CH(CH(CH3)2)CO2H (valine); and CH(CH2CO2H)CO2H (aspartic acid), were product yields high (greater than 10%). The yields of glycine were larger with R not equal to H. The prebiotic implications of these findings will be discussed.

  16. Insights into secondary organic aerosol formed via aqueous-phase reactions of phenolic compounds based on high resolution mass spectrometry

    Directory of Open Access Journals (Sweden)

    Y. Sun

    2010-02-01

    Full Text Available Recent work has shown that aqueous-phase reactions of phenolic compounds – phenol (C6H6O, guaiacol (C7H8O2, and syringol (C8H10O3 – can form secondary organic aerosol (SOA at high yields. Here we examine the chemical characteristics of this SOA and its formation mechanisms using a High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-AMS, an Ion Chromatograph (IC, and a Total Organic Carbon (TOC analyzer. The phenolic SOA are highly oxygenated with oxygen-to-carbon (O/C ratios in the range of 0.80–1.06 and carbon oxidation states (=2×O/C–H/C between −0.14 and +0.47. The organic mass-to-carbon (OM/OC ratios determined by the HR-AMS (=2.21���2.55 agree well with values determined based on the SOA mass measured gravimetrically and the OC mass from the TOC analyzer. Both the O/C and OM/OC ratios of the phenolic SOA are similar to the values observed for ambient low-volatility oxygenated/secondary OA (LV-OOA. Oxalate is a minor, but ubiquitous, component of the SOA formed from all three phenolic precursors, accounting for 1.4–5.2% of the SOA mass, with generally higher yields in experiments with H2O2 added as an ·OH source compared to without. The AMS spectra show evidence for the formation of syringol and guaiacol dimers and higher oligomers via C–C and C–O coupling of phenoxyl radicals, which are formed through oxidation pathways such as abstraction of the phenolic hydrogen atom or ·OH addition to the aromatic ring. This latter pathway leads to hydroxylation of the aromatic ring, which is one mechanism that increases the degree of oxidation of the SOA products. Compared to direct photochemical reactions of the phenols, ·OH-initiated reactions favor the formation of smaller oxidation products but less dimers or higher oligomers. Two unique and prominent ions in the syringol and guaiacol SOA spectra,

  17. Insights into secondary organic aerosol formed via aqueous-phase reactions of phenolic compounds based on high resolution mass spectrometry

    Directory of Open Access Journals (Sweden)

    Y. L. Sun

    2010-05-01

    Full Text Available Recent work has shown that aqueous-phase reactions of phenolic compounds – phenol (C6H6O, guaiacol (C7H8O2, and syringol (C8H10O3 – can form secondary organic aerosol (SOA at high yields. Here we examine the chemical characteristics of this SOA and its formation mechanisms using a High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-AMS, an Ion Chromatography system (IC, and a Total Organic Carbon (TOC analyzer. The phenolic SOA are highly oxygenated with oxygen-to-carbon (O/C ratios in the range of 0.80–1.06 and carbon oxidation states (=2×O/C-H/C between −0.14 and +0.47. The organic mass-to-carbon (OM/OC ratios determined by the HR-AMS (=2.21–2.55 agree well with values determined based on the SOA mass measured gravimetrically and the OC mass from the TOC analyzer. Both the O/C and OM/OC ratios of the phenolic SOA are similar to the values observed for ambient low-volatility oxygenated/secondary OA (LV-OOA. Oxalate is a minor, but ubiquitous, component of the SOA formed from all three phenolic precursors, accounting for 1.4−5.2% of the SOA mass, with generally higher yields in experiments with H2O2 added as an OH source compared to without. The AMS spectra show evidence for the formation of syringol and guaiacol dimers and higher oligomers via C-C and C-O coupling of phenoxyl radicals, which are formed through oxidation pathways such as abstraction of the phenolic hydrogen atom or OH addition to the aromatic ring. This latter pathway leads to hydroxylation of the aromatic ring, which is one mechanism that increases the degree of oxidation of the SOA products. Compared to direct photochemical reactions of the phenols, OH-initiated reactions favor the formation of smaller oxidation products but less dimers or higher oligomers. Two unique and prominent ions in the syringol and guaiacol SOA spectra, m/z 306 (C

  18. Application of the unwrapped phase inversion to land data without source estimation

    KAUST Repository

    Choi, Yunseok

    2015-08-19

    Unwrapped phase inversion with a strong damping was developed to solve the phase wrapping problem in frequency-domain waveform inversion. In this study, we apply the unwrapped phase inversion to band-limited real land data, for which the available minimum frequency is quite high. An important issue of the data is a strong ambiguity of source-ignition time (or source shift) shown in a seismogram. A source-estimation approach does not fully address the issue of source shift, since the velocity model and the source wavelet are updated simultaneously and interact with each other. We suggest a source-independent unwrapped phase inversion approach instead of relying on source-estimation from this land data. In the source-independent approach, the phase of the modeled data converges not to the exact phase value of the observed data, but to the relative phase value (or the trend of phases); thus it has the potential to solve the ambiguity of source-ignition time in a seismogram and work better than the source-estimation approach. Numerical examples show the validation of the source-independent unwrapped phase inversion, especially for land field data having an ambiguity in the source-ignition time.

  19. Bioethanol production from corn stover using aqueous ammonia pretreatment and two-phase simultaneous saccharification and fermentation (TPSSF).

    Science.gov (United States)

    Li, Xuan; Kim, Tae Hyun; Nghiem, Nhuan P

    2010-08-01

    An integrated bioconversion process was developed to convert corn stover derived pentose and hexose to ethanol effectively. In this study, corn stover was pretreated by soaking in aqueous ammonia (SAA), which retained glucan ( approximately 100%) and xylan (>80%) in the solids. The pretreated carbohydrates-rich corn stover was converted to ethanol via two-phase simultaneous saccharification and fermentation (TPSSF). This single-reactor process employed sequential simultaneous saccharification and fermentation (SSF), i.e. pentose conversion using recombinant Escherichia coli KO11 in the first phase, followed by hexose conversion with Saccharomyces cerevisiae D5A in the second phase. In the first phase, 88% of xylan digestibility was achieved through the synergistic action of xylanase and endo-glucanase with minimal glucan hydrolysis (10.5%). Overall, the TPSSF using 12-h SAA-treated corn stover resulted in the highest ethanol concentration (22.3g/L), which was equivalent to 84% of the theoretical ethanol yield based on the total carbohydrates (glucan+xylan) in the untreated corn stover.

  20. Extraction and purification of anthraquinones derivatives from Aloe vera L. using alcohol/salt aqueous two-phase system.

    Science.gov (United States)

    Tan, Zhi-jian; Li, Fen-fang; Xu, Xue-lei

    2013-08-01

    An alcohol/salt aqueous two-phase system (ATPS) composed of 1-propanol and (NH4)2SO4 was employed to purify anthraquinones (AQs) extracted from Aloe vera L. The main influencing system parameters such as type of alcohol, type and concentration of salt, temperature and pH were investigated in detail. Under the optimal extraction conditions, AQs can be extracted into alcohol-rich phase with high extraction efficiency, meanwhile majority polysaccharides, proteins, mineral substances and other impurities were extracted into salt-rich phase. Partitioning of AQs is dependent on hydrophobic interaction, hydrogen bond interaction, and salting-out effect in ATPS. Temperature also played a great role in the partitioning. After ATPS extraction, alcohol can be recycled by evaporation; moreover, salt can be recycled by dilution crystallization method. Compared with other liquid-liquid extractions, this alcohol/salt system is much simpler, lower in cost with easier recovery of phase-forming components, which has the potential scale-up in down-processing of active ingredients in plant.

  1. Integrated downstream processing of lactoperoxidase from milk whey involving aqueous two-phase extraction and ultrasound-assisted ultrafiltration.

    Science.gov (United States)

    Nandini, K E; Rastogi, Navin K

    2011-01-01

    The present work involves the adoption of an integrated approach for the purification of lactoperoxidase from milk whey by coupling aqueous two-phase extraction (ATPE) with ultrasound-assisted ultrafiltration. The effect of system parameters of ATPE such as type of phase system, polyethylene glycol (PEG) molecular mass, system pH, tie line length and phase volume ratio was evaluated so as to obtain differential partitioning of contaminant proteins and lactoperoxidase in top and bottom phases, respectively. PEG 6000-potassium phosphate system was found to be suitable for the maximum activity recovery of lactoperoxidase 150.70% leading to 2.31-fold purity. Further, concentration and purification of enzyme was attempted using ultrafiltration. The activity recovery and purification factor achieved after ultrafiltration were 149.85% and 3.53-fold, respectively. To optimise productivity and cost-effectiveness of integrated process, influence of ultrasound for the enhancement of permeate flux during ultrafiltration was also investigated. Intermittent use of ultrasound along with stirring (2 min acoustic and 2 min stirring) resulted in increased permeate flux from 0.94 to 2.18 l/m(2) h in comparison to the ultrafiltration without ultrasound. The use of ultrasound during ultrafiltration resulted in increase in flux, but there was no significant change in activity recovery and purification factor. The integrated approach involving ATPE and ultrafiltration may prove to be a feasible method for the downstream processing of lactoperoxidase from milk whey.

  2. Structural phase transition of merocyanine J-aggregate induced by ion-recombination in the aqueous sub-phase

    Science.gov (United States)

    Kato, Noritaka; Saito, Kentaro; Uesu, Yoshiaki

    2000-08-01

    By using the sub-phase, which contains two different kinds of counter-ions, we found a reversible thermochromic transition between different J-aggregate states of amphiphilic merocyanine dye (MD) molecules in the monolayer at the air-water interface. This chromatic change is attributed to the structural phase transition of MD J-aggregate crystallites induced by the mutual recombination of different counter-ions to MD molecules. The drastic morphological change of the MD monolayer during the transition is revealed by the in-situ observation using a multipurpose non-linear optical microscope.

  3. Aqueous-Phase Reactions of Isoprene with Sulfoxy Radical Anions as a way of Wet Aerosol Formation in the Atmosphere

    Science.gov (United States)

    Kuznietsova, I.; Rudzinski, K. J.; Szmigielski, R.; Laboratory of the Environmental Chemistry

    2011-12-01

    Atmospheric aerosols exhibit an important role in the environment. They have implications on human health and life, and - in the larger scale - on climate, the Earth's radiative balance and the cloud's formation. Organic matter makes up a significant fraction of atmospheric aerosols (~35% to ~90%) and may originate from direct emissions (primary organic aerosol, POA) or result from complex physico-chemical processes of volatile organic compounds (secondary organic aerosol, SOA). Isoprene (2-methyl-buta-1,3-diene) is one of the relevant volatile precursor of ambient SOA in the atmosphere. It is the most abundant non-methane hydrocarbon emitted to the atmosphere as a result of living vegetation. According to the recent data, the isoprene emission rate is estimated to be at the level of 500 TgC per year. While heterogeneous transformations of isoprene have been well documented, aqueous-phase reactions of this hydrocarbon with radical species that lead to the production of new class of wet SOA components such as polyols and their sulfate esters (organosulfates), are still poorly recognized. The chain reactions of isoprene with sulfoxy radical-anions (SRA) are one of the recently researched route leading to the formation of organosulfates in the aqueous phase. The letter radical species originate from the auto-oxidation of sulfur dioxide in the aqueous phase and are behind the phenomenon of atmospheric acid rain formation. This is a complicated chain reaction that is catalyzed by transition metal ions, such as manganese(II), iron(III) and propagated by sulfoxy radical anions . The presented work addresses the chemical interaction of isoprene with sulfoxy radical-anions in the water solution in the presence of nitrite ions and nitrous acid, which are important trace components of the atmosphere. We showed that nitrite ions and nitrous acid significantly altered the kinetics of the auto-oxidation of SO2 in the presence of isoprene at different solution acidity from 2 to 8

  4. Adsorption of dissolved Reactive red dye from aqueous phase onto activated carbon prepared from agricultural waste.

    Science.gov (United States)

    Senthilkumaar, S; Kalaamani, P; Porkodi, K; Varadarajan, P R; Subburaam, C V

    2006-09-01

    The adsorption of Reactive red dye (RR) onto Coconut tree flower carbon (CFC) and Jute fibre carbon (JFC) from aqueous solution was investigated. Adsorption studies were carried out at different initial dye concentrations, initial solution pH and adsorbent doses. The kinetic studies were also conducted; the adsorption of Reactive red onto CFC and JFC followed pseudosecond-order rate equation. The effective diffusion coefficient was evaluated to establish the film diffusion mechanism. Quantitative removal of Reactive red dye was achieved at strongly acidic conditions for both the carbons studied. The adsorption isotherm data were fitted well to Langmuir isotherm and the adsorption capacity were found to be 181.9 and 200 mg/g for CFC and JFC, respectively. The overall rate of dye adsorption appeared to be controlled by chemisorption, in this case in accordance with poor desorption studies.

  5. Adsorption of Monobutyl Phthalate from Aqueous Phase onto Two Macroporous Anion-Exchange Resins

    Directory of Open Access Journals (Sweden)

    Zhengwen Xu

    2014-01-01

    Full Text Available As new emerging pollutants, phthalic acid monoesters (PAMs pose potential ecological and human health risks. In the present study, adsorption performance of monobutyl phthalate (MBP onto two macroporous base anion-exchange resins (D-201 and D-301 was discussed. It was found that the adsorption isotherms were best fitted by the Langmuir equation while the adsorption kinetics were well described by pseudo-first-order model. Analyses of sorption isotherms and thermodynamics proved that the adsorption mechanisms for DBP onto D-201 were ion exchange. However, the obtained enthalpy values indicate that the sorption process of MBP onto D-301 is physical adsorption. The equilibrium adsorption capacities and adsorption rates of DBP on two different resins increased with the increasing temperature of the solution. D-301 exhibited a higher adsorption capacity of MBP than D-201. These results proved that D-301, as an effective sorbent, can be used to remove phthalic acid monoesters from aqueous solution.

  6. Aqueous-Phase Reforming of Renewable Polyols for Production of Hydrogen using Platinum Catalysts

    NARCIS (Netherlands)

    Boga, D.A.

    2013-01-01

    Hydrogen has the potential to fuel the energy needs of a more sustainable society. As hydrogen is not found in nature in any appreciable quantities, this energy carrier needs to be produced from a primary energy source. Biomass can serve as a source for sustainable hydrogen production. In principle,

  7. Extraction of penicillin G by aqueous two-phase system of [Bmim]BF4/NaH2PO4

    Institute of Scientific and Technical Information of China (English)

    LIU Qingfen; HU Xuesheng; WANG Yuhong; YANG Ping; XIA Hansong; YU Jiang; LIU Huizhou

    2005-01-01

    A novel approach for the extraction of penicillin G by aqueous two-phase system comprised of hydrophilic ionic liquid [Bmim]BF4 (1-butyl-3- methylimidazolium tetrafluoroborate) and NaH2PO4 is reported. The effects of some important parameters involving the concentration of NaH2PO4, the concentration of penicillin G, the amount of [Bmim]BF4 on the formation of aqueous two-phase system and the extraction yield of penicillin were investigated. The primary result shows that the ATPS can take advantage of penicillin concentrated in upper phase at higher pH value for penicillin extraction from its aqueous solution without emulsification.

  8. A novel aqueous micellar two-phase system composed of surfactant and sorbitol for purification of pectinase enzyme from Psidium guajava and recycling phase components.

    Science.gov (United States)

    Amid, Mehrnoush; Murshid, Fara Syazana; Manap, Mohd Yazid; Hussin, Muhaini

    2015-01-01

    A novel aqueous two-phase system composed of a surfactant and sorbitol was employed for the first time to purify pectinase from Psidium guajava. The influences of different parameters, including the type and concentration of the surfactant and the concentration and composition of the surfactant/sorbitol ratio, on the partitioning behavior and recovery of pectinase were investigated. Moreover, the effects of system pH and the crude load on purification fold and the yield of purified pectinase were studied. The experimental results indicated that the pectinase was partitioned into surfactant-rich top phase, and the impurities were partitioned into the sorbitol-rich bottom phase with the novel method involving an ATPS composed of 26% (w/w) Triton X-100 and 23% (w/w) sorbitol at 54.2% of the TLL crude load of 20% (w/w) at pH 6.0. The enzyme was successfully recovered by this method with a high purification factor of 15.2 and a yield of 98.3%, whereas the phase components were also recovered and recycled at rates above 96%. This study demonstrated that this novel ATPS method can be used as an efficient and economical alternative to the traditional ATPS for the purification and recovery of the valuable enzyme.

  9. A Novel Aqueous Micellar Two-Phase System Composed of Surfactant and Sorbitol for Purification of Pectinase Enzyme from Psidium guajava and Recycling Phase Components

    Directory of Open Access Journals (Sweden)

    Mehrnoush Amid

    2015-01-01

    Full Text Available A novel aqueous two-phase system composed of a surfactant and sorbitol was employed for the first time to purify pectinase from Psidium guajava. The influences of different parameters, including the type and concentration of the surfactant and the concentration and composition of the surfactant/sorbitol ratio, on the partitioning behavior and recovery of pectinase were investigated. Moreover, the effects of system pH and the crude load on purification fold and the yield of purified pectinase were studied. The experimental results indicated that the pectinase was partitioned into surfactant-rich top phase, and the impurities were partitioned into the sorbitol-rich bottom phase with the novel method involving an ATPS composed of 26% (w/w Triton X-100 and 23% (w/w sorbitol at 54.2% of the TLL crude load of 20% (w/w at pH 6.0. The enzyme was successfully recovered by this method with a high purification factor of 15.2 and a yield of 98.3%, whereas the phase components were also recovered and recycled at rates above 96%. This study demonstrated that this novel ATPS method can be used as an efficient and economical alternative to the traditional ATPS for the purification and recovery of the valuable enzyme.

  10. High-Yield Synthesis of Silver Nanoparticles by Precipitation in a High-Aqueous Phase Content Reverse Microemulsion

    Directory of Open Access Journals (Sweden)

    Y. D. Sosa

    2010-01-01

    Full Text Available Silver nanoparticles were precipitated at 70°C in a reverse microemulsion containing a high concentration of 0.5 M silver nitrate aqueous solution, toluene as organic phase, and a mixture of surfactants sodium bis (2-ethylhexyl sulfosuccinate/sodium dodecyl sulfate (2/1, w/w. Nanoparticles were characterized by X-ray diffraction, atomic absorption spectroscopy, and high-resolution transmission electron microscopy. In spite of the high-water/surfactant molar ratio and concentration of silver nitrate solution used in this study, characterizations demonstrated that nanoparticles were silver crystals (purity >99% with 8.6–8.8 nm in average diameter and 2.9–4.7 nm in standard deviation. It is proposed that slow dosing rate of aqueous solution of precipitating agent and the small molecular volume of toluene attenuated both particle aggregation and polydispersity widening. Experimental yield of silver nanoparticles obtained in this study was much higher than theoretical yields calculated from available data in the literature on preparation of silver nanoparticles in reverse microemulsions.

  11. 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

    was lower than that of subtilisin which was probably due to its higher hydrophobicity and, hence, a stronger salting-out effect. The protein concentration in each of the two phases was correlated with a ''saturation''-type equation. The partition coefficient could be satisfactorily predicted, as a function...... of the overall protein concentration, by the ratio between the ''saturation'' equations of the two individual phases. Better correlations were obtained when an empirical sigmoidal Boltzmann equation was fitted to the data, since in virtually all cases the partition coefficient is constant at low protein...... with 3% w/w NaCl was used for alpha-amylase. The concentration of the protein in each of the phases affected its partition behavior. The pattern for the individual proteins was dependent on their physicochemical properties. In the top phase, maximum protein concentration was determined mainly by a steric...

  12. Cell separation in immunoaffinity partition in aqueous polymer two-phase systems

    Science.gov (United States)

    Karr, Laurel J.; Van Alstine, James M.; Snyder, Robert S.; Shafer, Steven G.; Harris, J. Milton

    1989-01-01

    Two methods for immunoaffinity partitioning are described. One technique involves the covalent coupling of poly (ethylene glycol) (PEG) to immunoglobulin G antibody preparations. In the second method PEG-modified Protein A is used to complex with cells and unmodified antibody. The effects of PEG molecular weight, the degree of modification, and varying phase system composition on antibody activity and its affinity for the upper phase are studied. It is observed that both methods resulted in effective cell separation.

  13. Investigation on the extraction of strontium ions from aqueous phase using crown ether-ionic liquid systems

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The extraction of strontium ions using DCH18C6 as the extractant and various ionic liquids(ILs) as solvents has been investigated.The distribution ratio of Sr2+ can reach as high as 103 under certain conditions,much larger than that in DCH18C6/n-octanol system.The extraction capacity depends greatly on the structure of ionic liquids.In Ils-based extraction systems,the extraction efficiency of strontium ions is reduced by increasing the concentration of nitric acid and can also be influenced directly by the presence of Na+ and K+ in the aqueous phase.It is confirmed that the extraction proceeds mainly via a cation-exchange mechanism.

  14. Transformation of Vesicles in Aqueous Two-Phase System of an Anionic Gemini Surfactant and a Cationic Conventional Surfactant Mixture

    Institute of Scientific and Technical Information of China (English)

    JIANG Rong; HUANG Yi-Xiong; ZHAO Jian-Xi; HUANG Chang-Cang

    2008-01-01

    Transformation of vesicles formed in DTAB/C11-p-PhCNa aqueous surfactant two-phase (ASTP) was observed by the transmission electron microscopy (TEM). The trans-conformation of the gemini surfactant in the aggregates was considered to be the important factor for constructing the multi-lamellar structure of the vesicle wall. The cation-π interaction between the quaternary ammonium cation and the aromatic ring in the spacer was determined by the UV-Vis spectrum analysis, which, as well as the general electrostatic attraction and hydrophobic force, contributes to the stability of the multi-lamellar structure. The concentrations of the surface-active ions were measured for understanding the mechanism of vesicle transformation. The results show that isoelectric mixing of the two components benefits the growth of vesicles both in size and wall thickness.

  15. Optimization of aqueous enzymatic oil extraction from kernel of oil palm (elaeis guineensis) using three phase partitioning and microwave

    International Nuclear Information System (INIS)

    The use of microwave irradiation as a pretreatment before aqueous enzymatic oil extraction from oil palm kernel was found to be useful. The microwave irradiation for 10 min -assisted extraction was found to be a simpler and more effective alternative to the solvent extraction methods for the productions of palm kernel oil. Further enhancement was achieved when the microwave irradiated slurries were treated with a commercial enzyme preparation of proteases, followed by three phase partitioning. This resulted in 93% (w/w) oil yields form the palm kernel. The efficiency of the present technique is comparable to solvent extraction with an added advantage of being less time consuming and using t-butanol which is a safer solvent as compared to n-hexane used in conventional oil extraction process. The technique also tries to reduce the amount of enzyme used and hence reduces the overall cost. (author)

  16. Base-Free Aqueous-Phase Oxidation of 5-Hydroxymethylfurfural over Ruthenium Catalysts Supported on Covalent Triazine Frameworks.

    Science.gov (United States)

    Artz, Jens; Palkovits, Regina

    2015-11-01

    The base-free aqueous-phase oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxilic acid (FDCA) was performed at 140 °C and 20 bar of synthetic air as the oxidant. Ru clusters supported on covalent triazine frameworks (CTFs) enabled superior conversion (99.9%) and FDCA yields in comparison to other support materials such as activated carbon and γ-Al2O3 after only 1 h. The properties of the CTFs such as pore volume, specific surface area, and polarity could be tuned by using different monomers. These material properties influence the catalytic activity of Ru/CTF significantly as mesoporous CTFs showed superior activity compared to microporous materials, whereas high polarities provide further beneficial effects. The recyclability of the prepared Ru/CTF catalysts was comparable to that of Ru/C at high conversions and product yields. Nevertheless, minor deactivation in five successive recycling experiments was observed. PMID:26482331

  17. Aqueous Phase Glycerol Reforming by PtMo Bimetallic Nano-Particle Catalyst: Product Selectivity and Structural Characterization

    Energy Technology Data Exchange (ETDEWEB)

    Stach E. A.; Dietrich, P.J.; Lobo-Lapidus, R.J.; Wu, T.; Sumer, A.; Akatay, M.C.; Fingland, B.R.; Guo, N.; Dumesic, J.A.; Marshall, C.L.; Jellinek, J.; Delgass, W.N.; Ribeiro, F.H.; Miller, J.T.

    2012-03-01

    A carbon supported PtMo aqueous phase reforming catalyst for producing hydrogen from glycerol was characterized by analysis of the reaction products and pathway, TEM, XPS and XAS spectroscopy. Operando X-ray absorption spectroscopy (XAS) indicates the catalyst consists of bimetallic nano-particles with a Pt rich core and a Mo rich surface. XAS of adsorbed CO indicates that approximately 25% of the surface atoms are Pt. X-ray photoelectron spectroscopy indicates that there is unreduced and partially reduced Mo oxide (MoO{sub 3} and MoO{sub 2}), and Pt-rich PtMo bimetallic nano-particles. The average size measured by transmission electron microscopy of the fresh PtMo nano-particles is about 2 nm, which increases in size to 5 nm after 30 days of glycerol reforming at 31 bar and 503 K. The catalyst structure differs from the most energetically stable structure predicted by density functional theory (DFT) calculations for metallic Pt and Mo atoms. However, DFT indicates that for nano-particles composed of metallic Pt and Mo oxide, the Mo oxide is at the particle surface. Subsequent reduction would lead to the experimentally observed structure. The aqueous phase reforming reaction products and intermediates are consistent with both C-C and C-OH bond cleavage to generate H{sub 2}/CO{sub 2} or the side product CH{sub 4}. While the H{sub 2} selectivity at low conversion is about 75%, cleavage of C-OH bonds leads to liquid products with saturated carbon atoms. At high conversions (to gas), these will produced additional CH{sub 4} reducing the H{sub 2} yield and selectivity.

  18. Fourier Transform Infrared Spectroscopy for Identification and Quantification of Organic Functional Groups in Aqueous Phase Secondary Organic Aerosol

    Science.gov (United States)

    George, K.; Ruthenburg, T. C.; Smith, J.; Anastasio, C.; Dillner, A. M.

    2011-12-01

    Particles in the atmosphere influence visibility, climate, and human health. Secondary organic aerosols (SOA) formed from chemical reactions in the atmosphere constitute a portion of total organic particle mass. Most research on SOA has focused on gas phase reactions; however, reactions taking place in cloud and fog drops may be significant. One group of water-soluble compounds that participate in these reactions is phenols. Phenols, emitted from biomass burning, react in the aqueous phase to form low-volatility SOA products. The products formed from these reactions are currently poorly characterized. In order to characterize laboratory-generated samples, we are developing an attenuated total reflectance-Fourier transform infrared spectroscopic (ATR-FTIR) technique to identify and quantify organic functional groups in SOA. Aqueous SOA is made in the laboratory by illuminating solutions of phenolic compounds with an oxidant. The illuminated solution is then blown to dryness in order to determine the mass of SOA produced. The dry SOA is reconstituted in water and drops of this solution are placed onto a single-reflection ATR accessory. In order to identify and quantify functional groups in the complex SOA samples, it is necessary to calibrate with compounds and mixtures of compounds containing bond types similar to those found in the laboratory-generated SOA. Initially, focus has been placed on multiple peaks located in the region between 1800 cm-1 and 800 cm-1, including peaks for C=O and C-O. We distinguish between characteristic absorbances to begin determining the organic functional group composition of the SOA samples. This ATR-FTIR technique complements information from mass spectrometry measurements and allows us to quantify organic mass for non-volatile SOA products.

  19. The diastereomers of mannosylerythritol lipids have different interfacial properties and aqueous phase behavior, reflecting the erythritol configuration.

    Science.gov (United States)

    Fukuoka, Tokuma; Yanagihara, Takashi; Imura, Tomohiro; Morita, Tomotake; Sakai, Hideki; Abe, Masahiko; Kitamoto, Dai

    2012-04-01

    Mannosylerythritol lipids (MELs) produced by yeasts are one of the most promising glycolipid biosurfactants. There are two MEL diastereomers, in which the configurations of the erythritol moieties are opposite. The 4-O-β-D-mannopyranosyl-(2S,3R)-erythritol (S-form) or 4-O-β-D-mannopyranosyl-(2R,3S)-erythritol (R-form) is the hydrophilic domain. In this study, we prepared S- and R-form MEL homologs with similar fatty acyl groups, and compared their interfacial properties. Among the four diastereomers (S-MEL-B and -D/R-MEL-B and -D), R-form MELs showed a higher critical aggregation concentration and hydrophilicity compared to the corresponding S-form. R-form MELs also efficiently formed relatively large vesicles compared to S-form. Moreover, we estimated the binary phase diagram of the MEL-water system and compared the aqueous phase behavior among the four diastereomers. The present MELs self-assembled into a lamellar (L(α)) structure at all concentration ranges. Meanwhile, the one-phase L(α) region of R-form MELs was wider than those of S-form MELs. R-form MELs may maintain more water between the polar layers in accordance with an extension of the interlayer spacing. These results suggest that the differences in MEL carbohydrate configurations significantly affect interfacial properties, self-assembly, and hydrate ability. PMID:22341919

  20. Aqueous Phase Synthesis and Enhanced Field Emission Properties of ZnO-Sulfide Heterojunction Nanowires.

    Science.gov (United States)

    Wang, Guojing; Li, Zhengcao; Li, Mingyang; Chen, Chienhua; Lv, Shasha; Liao, Jiecui

    2016-01-01

    ZnO-CdS, ZnO-ZnS, and ZnO-Ag2S core-shell heterojunction structures were fabricated using low-temperature, facile and simple aqueous solution approaches. The polycrystalline sulfide shells effectively enhance the field emission (FE) properties of ZnO nanowires arrays (NWAs). This results from the formation of the staggered gap heterointerface (ZnO-sulfide) which could lead to an energy well at the interfaces. Hence, electrons can be collected when an electric field is applied. It is observed that ZnO-ZnS NWAs have the lowest turn-on field (3.0 Vμm(-1)), compared with ZnO-CdS NWAs (6.3 Vμm(-1)) and ZnO-Ag2S NWAs (5.0 Vμm(-1)). This may be associated with the pyramid-like ZnS shell which increases the number of emission nanotips. Moreover, the Fowler-Nordheim (F-N) plot displays a nonlinear relationship in the low and high electric field regions caused by the double well potential effect of the heterojunction structures. PMID:27387653

  1. Green synthesis of copper nanoparticles for the efficient removal (degradation) of dye from aqueous phase.

    Science.gov (United States)

    Sinha, Tanur; Ahmaruzzaman, M

    2015-12-01

    The present work reports the utilization of a common household waste material (fish scales of Labeo rohita) for the synthesis of copper nanoparticles. The method so developed was found to be green, environment-friendly, and economic. The fish scale extracts were acting as a stabilizing and reducing agents. This method avoids the use of external reducing and stabilizing agents, templates, and solvents. The compositional abundance of gelatin may be envisaged for the effective reductive as well as stabilizing potency. The mechanisms for the formation of nanoparticles have also been presented. The synthesized copper nanoparticles formed were predominantly spherical in nature with an average size of nanoparticles in the range of 25-37 nm. The copper nanoparticles showed characteristic Bragg's reflection planes of fcc which was supported by both selected area electron diffraction and X-ray diffraction pattern and showed surface plasmon resonance at 580 nm. Moreover, the energy dispersive spectroscopy pattern also revealed the presence of only elemental copper in the copper nanoparticles. The prepared nanoparticles were used for the remediation of a carcinogenic and noxious textile dye, Methylene blue, from aqueous solution. Approximately, 96 % degradation of Methylene blue dye was observed within 135 min using copper nanoparticles. The probable mechanism for the degradation of the dye has been presented, and the degraded intermediates have been identified using the liquid chromatography-mass spectroscopy technique. The high efficiency of nanoparticles as photocatalysts has opened a promising application for the removal of hazardous dye from industrial effluents contributing indirectly to environmental cleanup process.

  2. Irradiation of ultrasound to 5-methylbenzotriazole in aqueous phase: Degradation kinetics and mechanisms.

    Science.gov (United States)

    Kim, Duk K; He, Yingxin; Jeon, Junho; O'Shea, Kevin E

    2016-07-01

    Ultrasonic irradiation (640 kHz) leads to the effective degradation of 5-methyl-benzotriazole (5-MBT) in O2 saturated aqueous solution. Up to 97% of 5-MBT is eliminated within 2h of treatment. Upon extended treatment of 6h, UV absorbance of the n→π(∗) and π→π(∗) transitions associated with aromatic and conjugated systems are completely removed, indicating complete destruction of the aromatic system in 5-MBT. The decomposition of 5-MBT follows pseudo-first order kinetics and the observed decomposition rate dropped significantly in the presence of tertiary butyl alcohol. Detailed product studies were performed employing a negative mode ESI LC-MS. Twenty eight intermediate products were detected during ultrasonic mediated degradation of 5-MBT. Reaction pathways are proposed based on the structures of products assigned to observed 28 masses from LC-MS and commonly accepted degradation pathways observed by thermal and hydroxyl radical mediated pathways often associated with ultrasonic treatment. PMID:26964945

  3. Secondary Organic Aerosol Formation from Acetylene (C2H2: seed effect on SOA yields due to organic photochemistry in the aerosol aqueous phase

    Directory of Open Access Journals (Sweden)

    P. J. Ziemann

    2009-03-01

    Full Text Available The lightest Non Methane HydroCarbon (NMHC, i.e., acetylene (C2H2 is found to form secondary organic aerosol (SOA. Contrary to current belief, the number of carbon atoms, n, for a NMHC to act as SOA precursor is lowered to n=2 here. The OH-radical initiated oxidation of C2H2 forms glyoxal (CHOCHO as the highest yield product, and >99% of the SOA from C2H2 is attributed to CHOCHO. SOA formation from C2H2 and CHOCHO was studied in a photochemical and a dark simulation chamber. Further, the experimental conditions were varied with respect to the chemical composition of the seed aerosols, mild acidification with sulphuric acid (SA, 3source from CHOCHO, while seeds containing amino acids (AA and/or SA showed among the lowest of all YSOA values, and largely suppress the photochemical enhancement on the rate of CHOCHO uptake. Our results give first evidence for the importance of heterogeneous photochemistry of CHOCHO in SOA formation, and identify a potential bias in the currently available YSOA data for other SOA precursor NMHCs. We demonstrate that SOA formation via the aqueous phase is not limited to cloud droplets, but proceeds also in the absence of clouds, i.e., does not stop once a cloud droplet evaporates. Atmospheric models need to be expanded to include SOA formation from WSOC photochemistry of CHOCHO, and possibly other α-dicarbonyls, in aqueous aerosols.

  4. Valorization of the aqueous phase obtained from hydrothermally treated Dunaliella salina remnant biomass.

    Science.gov (United States)

    Pirwitz, Kristin; Rihko-Struckmann, Liisa; Sundmacher, Kai

    2016-11-01

    Up to 90% of Dunaliella salina biomass remains unused after extraction of the main product β-carotene. The potential of mild hydrothermal liquefaction (HTL) to exploit this biomass as a source of valuable by-products was assessed. The results indicate that 80% of the remnant was converted into glucose by mild HTL (100°C, 0min). The recovered glucose was successfully used as a carbon source to cultivate biotechnologically relevant microorganisms, namely Chlorella vulgaris, Escherichia coli and Saccharomyces cerevisiae. Furthermore, the analysis of energy demand and operating costs confirms the beneficial effect of mild liquefaction on the overall process economics of algal β-carotene production. PMID:27475332

  5. A study of iodine, cesium, and strontium sorption on alkali-earth hydro-phosphates from the aqueous phase

    International Nuclear Information System (INIS)

    Full text of publication follows: The amount of radioactive species penetrating into the environment because of human activities has been increasingly growing. The most biologically dangerous nuclear-fuel fission products are iodine, cesium, and strontium radionuclides, which can sorb from aqueous solutions on various natural objects, including apatite minerals. This work studied the sorption of 131I-, 131IO3-137Cs+ and 85Sr2+ ions of various samples of Ca, Sr, and Ba hydro-phosphates. The samples of alkali-earth hydro-phosphates (AEHP) were synthesized by the following reactions: MCl2 + Na3PO4 + NaOH → M5(PO4)3OH↓; MCl2 + NH4OH + (NH4)2HPO4 → M5(PO4)3OH↓; MCl2 + NaOH + (NH4)2HPO4 → M5(PO4)3OH↓ (where M is Ca, Sr, or Ba). The experiments on a study of the sorption of 131I-, 131IO3-137Cs+, and 85Sr2+ ions on AEHP from aqueous solutions of KI, KIO3, CsNO3, or Sr(NO3)2 were carried out using the following procedure. A calculated amount of the target AEHP was added upon mixing to a 1.10-5 mg/dm3 water solution (200 ml) of KI, KIO3, CsNO3, or Sr(NO3)2 containing the radionuclides 131I, 137Cs, and 85Sr. The calculation of the AEHP was carried out based on the condition that the ratio between the volume of the liquid and the weight of the solid phase V/m was equal to 500 or 200 ml/g. The suspension was actively mixed over the necessary period of time, and the precipitate was then filtered off. The precipitate on the filter was washed two times with 50-ml portions of water, which were merged in one fraction with the filtered matter. Following that, the concentrations of 131I, 137Cs and 85Sr radionuclides in the solution and precipitate were measured using a gamma spectrometric study. Using the known V/m ratio and the distribution of radionuclides between the solid and liquid phases, the distribution coefficient Kd was calculated by the formula: Kd = V/m . I1/I2, where I1 and I2 are the concentrations of radionuclides in the solid and liquid phases, respectively

  6. Tetracycline degradation by ozonation in the aqueous phase: Proposed degradation intermediates and pathway

    International Nuclear Information System (INIS)

    During the ozonation of tetracycline (TC) in aqueous media at pHs 2.2 and 7.0, the effects of pH variations, protonation and dissociation of functional groups and variation in free radical exposure were investigated to elucidate the transformation pathway. Liquid chromatography-triple quadrupole mass spectrometry detected around 15 ozonation products, and uncovered their production and subsequent degradation patterns. During ozonation at pH 2.2, the TC degradation pathway was proposed on the basis of the structure, ozonation chemistry and mass spectrometry data of TC. Ozonation of TC at the C11a-C12 and C2-C3 double bonds, aromatic ring and amino group generated products of m/z 461, 477, 509 and 416, respectively. Further ozonation at the above mentioned sites gave products of m/z 432, 480, 448, 525 and 496. The removal of TOC reached a maximum of ∼40% after 2 h of ozonation, while TC was completely removed within 4-6 min at both pHs. The low TOC removal efficiency might be due to the generation of recalcitrant products and the low ozone supply for high TC concentration. Ozonation decreased the acute toxicity of TC faster at pH 7.0 than pH 2.2, but the maximum decrease was only about 40% at both pHs after 2 h of ozonation. In this study, attempts were made to understand the correlation between the transformation products, pathway, acute toxicity and quantity of residual organics in solution. Overall, ozonation was found to be a promising process for removing TC and the products initially generated.

  7. Tetracycline degradation by ozonation in the aqueous phase: Proposed degradation intermediates and pathway

    Energy Technology Data Exchange (ETDEWEB)

    Khan, M. Hammad; Bae, Hyokwan [Water Environment Center, Korea Institute of Science and Technology, 39-1 Hawolgok-Dong, Seongbuk-Gu, Seoul 136-791 (Korea, Republic of); Jung, Jin-Young, E-mail: jinjung@ynu.ac.kr [Department of Environmental Engineering, Yeungnam University, 214-1 Dae-Dong, Gyeongsan-Si, Gyeongsangbuk-Do 712-749 (Korea, Republic of)

    2010-09-15

    During the ozonation of tetracycline (TC) in aqueous media at pHs 2.2 and 7.0, the effects of pH variations, protonation and dissociation of functional groups and variation in free radical exposure were investigated to elucidate the transformation pathway. Liquid chromatography-triple quadrupole mass spectrometry detected around 15 ozonation products, and uncovered their production and subsequent degradation patterns. During ozonation at pH 2.2, the TC degradation pathway was proposed on the basis of the structure, ozonation chemistry and mass spectrometry data of TC. Ozonation of TC at the C11a-C12 and C2-C3 double bonds, aromatic ring and amino group generated products of m/z 461, 477, 509 and 416, respectively. Further ozonation at the above mentioned sites gave products of m/z 432, 480, 448, 525 and 496. The removal of TOC reached a maximum of {approx}40% after 2 h of ozonation, while TC was completely removed within 4-6 min at both pHs. The low TOC removal efficiency might be due to the generation of recalcitrant products and the low ozone supply for high TC concentration. Ozonation decreased the acute toxicity of TC faster at pH 7.0 than pH 2.2, but the maximum decrease was only about 40% at both pHs after 2 h of ozonation. In this study, attempts were made to understand the correlation between the transformation products, pathway, acute toxicity and quantity of residual organics in solution. Overall, ozonation was found to be a promising process for removing TC and the products initially generated.

  8. Cluster, glass, and gel formation and viscoelastic phase separation in aqueous clay suspensions.

    Science.gov (United States)

    Shalkevich, Andrey; Stradner, Anna; Bhat, Suresh Kumar; Muller, François; Schurtenberger, Peter

    2007-03-27

    We have systematically investigated the phase diagram of clay particles in water to understand the relation between the local and macroscopic properties and the structures of clay suspensions. We focused, in particular, on sodium Cloisite (CNa) particles at concentrations typically used in nanocomposites (concentrations from 1 to 4 wt %) and at an extended range of ionic strengths (10(-5) to 10(-2) M NaCl). The suspensions have been characterized using rheology and a combination of scattering techniques (neutrons, X-rays, and light). We demonstrate the existence of a liquid cluster phase at low clay and intermediate salt concentrations and provide new insight into the nature of the solid-like dispersions at low and high ionic strengths.

  9. Concentration selective hydration and phase states of hydroxyethyl cellulose (HEC) in aqueous solutions.

    Science.gov (United States)

    Arfin, Najmul; Bohidar, H B

    2012-04-01

    Solution behaviour of hydroxyethyl cellulose (HEC) is reported in the polymer concentration range spanning over two decades (c=0.002-5% (w/v)). The results conclude the following: (i) dilute solution regime prevailed for cCole-Cole plots revealed phase homogeneity and miscibility was limited to concentrations less than ~2% (w/v). For higher polymer concentrations, strong fibre-fibre interactions prevailed and samples became heterogeneous.

  10. Linker Length-Dependent Control of Gemini Surfactant Aqueous Lyotropic Gyroid Phase Stability.

    Science.gov (United States)

    Perroni, Dominic V; Baez-Cotto, Carlos M; Sorenson, Gregory P; Mahanthappa, Mahesh K

    2015-03-19

    Network-phase lyotropic liquid crystals (LLCs) derived from the water-directed self-assembly of small molecule amphiphiles comprise a useful class of soft nanomaterials, with wide-ranging applications in structural biology and membrane science. However, few known surfactants enable access to these mesophases over wide temperature and amphiphile concentration phase windows. Recent studies have demonstrated that gemini ("twin tail") dicarboxylate surfactants, in which alkyl carboxylates are covalently linked near the headgroups by a hydrophobic bridge, exhibit increased propensities to form double gyroid network phase LLCs. We demonstrate herein that the lyotropic self-assembly behaviors of gemini dicarboxylates sensitively depend on the linker length, whereby odd-carbon linkers stabilize the double gyroid network LLC over unprecedented amphiphile concentration windows up to ∼45 wt % wide between T ≈ 22-80 °C. These self-assembly phenomena, which arise from the linker length-dependent preferred molecular conformations of these amphiphiles, will broaden the technological applications of these nanostructured LLCs. PMID:26262858

  11. Recovery of laccase from processed Hericium erinaceus (Bull.:Fr) Pers. fruiting bodies in aqueous two-phase system.

    Science.gov (United States)

    Rajagopalu, Devamalini; Show, Pau Loke; Tan, Yee Shin; Muniandy, Sekaran; Sabaratnam, Vikineswary; Ling, Tau Chuan

    2016-09-01

    The feasible use of aqueous two-phase systems (ATPSs) to establish a viable protocol for the recovery of laccase from processed Hericium erinaceus (Bull.:Fr.) Pers. fruiting bodies was evaluated. Cold-stored (4.00±1.00°C) H. erinaceus recorded the highest laccase activities of 2.02±0.04 U/mL among all the processed techniques. The evaluation was carried out in twenty-five ATPSs, which composed of polyethylene glycol (PEG) with various molecular weights and potassium phosphate salt solution to purify the protein from H. erinaceus. Optimum recovery condition was observed in the ATPS which contained 17% (w/w) PEG with a molecular weight of 8000 and 12.2% (w/w) potassium phosphate solution, at a volume ratio (VR) of 1.0. The use of ATPS resulted in one-single primary recovery stage process that produced an overall yield of 99% with a purification factor of 8.03±0.46. The molecular mass of laccases purified from the bottom phase was in the range of 55-66 kDa. The purity of the partitioned laccase was confirmed with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). PMID:26922478

  12. Production of dry Lactobacillus rhamnosus GG preparations by spray drying and lyophilization in aqueous two-phase systems

    Directory of Open Access Journals (Sweden)

    Katarzyna Leja

    2009-12-01

    Full Text Available Background. Drying is the oldest method of food preservation. It works by removing water from the food, which prevents the growth of microorganisms and decay. Moreover, spray or freeze drying is also used for the preservation of probiotic cultures. The aim of this study was to compare a survival rate of probiotic bacteria Lactobacillus rhamnosus during spray and freeze drying in ATPS. These results were also compared with survival rate of cells dried under the same conditions but suspended only in skim milk, 6% solution of PVP or 6% solution of dextran. Material and methods. The bacteria Lactobacillus rhamnosus GGwere suspended and spray or freeze dried in various types of aqueous two-phase emulsions: PVP/dextran, PEG4000/dextran and PEG8000/dextran. These emulsions consisted of different types of polymers and had varying ratio of polymers in dispersed (dextran and dispersing (PEG and PVP phases. Results. The research demonstrated that survival rate of bacteria directly after drying depended mainly on protective reagent, rather than on drying method. After 30-day-storage of the dried bacteria cell specimens, the highest survival rate was noted in case of freeze dried cells in milk. In case of spray drying the highest cell survival rate was observed when emulsion PVP3.6%/dextran2.4% was used as a drying medium. Conclusions. Finally, it has been found that cell survival rate was not strongly influenced by the storage temperature of the powder but it depended on the drying medium.  

  13. 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.

  14. Instability of Solution of Phase Retrieval in Direct Diffraction Phase-Contrast Imaging with Partially Coherent X-Ray Source

    Institute of Scientific and Technical Information of China (English)

    GUO Hua; HAN Shen-Sheng

    2006-01-01

    The theoretical model of direct diffraction phase-contrast imaging with partially coherent x-ray source is expressedby an operator of multiple integral. It is presented that the integral operator is linear. The problem of its phaseretrieval is described by solving an operator equation of multiple integral. It is demonstrated that the solution ofthe phase retrieval is unstable. The numerical simulation is performed and the result validates that the solutionof the phase retrieval is unstable.

  15. Characterisation of UV-cured acrylate networks by means of hydrolysis followed by aqueous size-exclusion combined with reversed-phase chromatography.

    NARCIS (Netherlands)

    R. Peters; V.M. Litvinov; P. Steeman; A.A. Dias; Y. Mengerink; R. van Benthem; C.G. de Koster; S. van der Wal; P.J. Schoenmakers

    2007-01-01

    UV-cured networks prepared from mixtures of di-functional (polyethylene-glycol di-acrylate) and mono-functional (2-ethylhexyl acrylate) acrylates were analysed after hydrolysis, by aqueous size-exclusion chromatography coupled to on-line reversed-phase liquid-chromatography. The mean network density

  16. Cluster, glass, and gel formation and viscoelastic phase separation in aqueous clay suspensions

    OpenAIRE

    Shalkevich, Andrey; Stradner, Anna; Bhat, Suresh Kumar; MULLER, François; Schurtenberger, Peter

    2008-01-01

    We have systematically investigated the phase diagram of clay particles in water to understand the relation between the local and macroscopic properties and the structures of clay suspensions. We focused, in particular, on sodium Cloisite (CNa) particles at concentrations typically used in nanocomposites (concentrations from 1 to 4 wt %) and at an extended range of ionic strengths (10⁻⁵ to 10⁻² M NaCl). The suspensions have been characterized using rheology and a combination of scattering tec...

  17. Use of a Combined Technology of Ultrasonication, Three-Phase Partitioning, and Aqueous Enzymatic Oil Extraction for the Extraction of Oil from Spirogyra sp.

    OpenAIRE

    Adisheshu Reddy; Majumder, Abir B

    2014-01-01

    Algal oil from Spirogyra sp. was extracted using a combined technology of ultrasonication, three-phase partitioning, and aqueous enzymatic oil extraction. Ultrasonication was done to rupture the cell wall and papain was used for an easier release of the trapped oil. The salt concentration for three-phase partitioning, preincubation period with (or without) the protease, and its operational temperature were optimized for a maximum possible yield of the oil and the effect of ultrasonication, an...

  18. Enzymatic synthesis of a novel glycolipid biosurfactant, mannosylerythritol lipid-D and its aqueous phase behavior.

    Science.gov (United States)

    Fukuoka, Tokuma; Yanagihara, Takashi; Imura, Tomohiro; Morita, Tomotake; Sakai, Hideki; Abe, Masahiko; Kitamoto, Dai

    2011-02-01

    Mannosylerythritol lipids (MELs) produced by yeasts are one of the most promising glycolipid biosurfactants. In this study, we succeeded in the preparation of a novel MEL homolog having no acetyl groups, namely MEL-D. MEL-D was synthesized by lipase-catalyzed hydrolysis of acetyl groups from a known MEL, and identified as 4-O-[2',3'-di-O-alka(e)noyl-β-d-mannopyranosyl]-(2R,3S)-erythritol. The obtained MEL-D showed a higher critical aggregation concentration (CAC=1.2 × 10(-5)M) and hydrophilicity compared to known MELs, retaining an excellent surface tension lowering activity (the surface tension at the CAC was 24.5mN/m). In addition, we estimated the binary phase diagram of the MEL-D-water system based on a combination of visual inspection, polarized optical microscopy, and SAXS measurement. From these results, MEL-D was found to self-assemble into a lamellar (L(α)) structure over all ranges of concentration. Meanwhile, the one-phase L(α) region of MEL-D was extended wider than those of known MELs. MEL-D might keep more water between the polar layers in accordance with the extension of the interlayer spacing (d). These results suggest that the newly obtained MEL-D would facilitate the application of MELs in various fields as a lamellar-forming glycolipid with higher hydrate ability. PMID:21163471

  19. Comparison of iso-eluotropic mobile phases at different temperatures for the separation of triacylglycerols in Non-Aqueous Reversed Phase Liquid Chromatography.

    Science.gov (United States)

    Hmida, Dorra; Abderrabba, Manef; Tchapla, Alain; Héron, Sylvie; Moussa, Fathi

    2015-05-15

    Triacylglycerols (TAGs) are a large class of neutral lipids that naturally occur in both plant and animal oils and fats. Their analyses in Non-Aqueous Reversed Phase Liquid Chromatography (NARP) require a mixture of weak solvent (mostly acetonitrile) and strong solvent. In the present work, we have established eluotropic solvent strength scale of several binary mobile phases on C18 bonded silica at different temperatures (acetonitrile/methylene chloride, acetonitrile/acetone, acetonitrile/ethyl acetate, acetonitrile/propan-2-ol, and acetonitrile/butan-1-ol at 25°C, 43°C, 63°C and 85°C); it is based on the methylene selectivity and the use of homologous series. We show that this scale is well suited to the TAGs analysis. The analysis of nine seed oils (Aleurites fordii, Calophyllum inophyllum, Glycina max, Olea europea, Orbignya olifeira, Pinus koraiensis, Pistacia lentiscus, Punica granatum and Ribes nigrum) in iso-eluotropic conditions leads to propose unambiguously the couple MeCN/BuOH at 25°C as the best system to separate TAGs. The use of butanol, as strong solvent, provides very good TAGs congeners separations and avoids the use of chlorinated solvents which gave to this day the best separations. PMID:25855317

  20. Evaluating the potential for quantitative monitoring of in situ chemical oxidation of aqueous-phase TCE using in-phase and quadrature electrical conductivity

    Science.gov (United States)

    Hort, R. D.; Revil, A.; Munakata-Marr, J.; Mao, D.

    2015-07-01

    Electrical resistivity measurements can potentially be used to remotely monitor fate and transport of ionic oxidants such as permanganate (MnO4-) during in situ chemical oxidation (ISCO) of contaminants like trichloroethene (TCE). Time-lapse two-dimensional bulk conductivity and induced polarization surveys conducted during a sand tank ISCO simulation demonstrated that MnO4- plume movement could be monitored in a qualitative manner using bulk conductivity tomograms, although chargeability was below sensitivity limits. We also examined changes to in-phase and quadrature electrical conductivity resulting from ion injection, MnO2 and Cl- production, and pH change during TCE and humate oxidation by MnO4- in homogeneous aqueous solutions and saturated porous media samples. Data from the homogeneous samples demonstrated that inversion of the sand tank resistivity data using a common Tikhonov regularization approach was insufficient to recover an accurate conductivity distribution within the tank. While changes to in-phase conductivity could be successfully modeled, quadrature conductivity values could not be directly related to TCE oxidation product or MnO4- concentrations at frequencies consistent with field induced polarization surveys, limiting the utility of quadrature conductivity for monitoring ISCO.

  1. 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.

  2. Diffusion-regulated phase-transfer catalysis for atom transfer radical polymerization of methyl methacrylate in an aqueous/organic biphasic system.

    Science.gov (United States)

    Ding, Mingqiang; Jiang, Xiaowu; Peng, Jinying; Zhang, Lifen; Cheng, Zhenping; Zhu, Xiulin

    2015-03-01

    A concept based on diffusion-regulated phase-transfer catalysis (DRPTC) in an aqueous-organic biphasic system with copper-mediated initiators for continuous activator regeneration is successfully developed for atom transfer radical polymerization (ICAR ATRP) (termed DRPTC-based ICAR ATRP here), using methyl methacrylate (MMA) as a model monomer, ethyl α-bromophenylacetate (EBrPA) as an initiator, and tris(2-pyridylmethyl)amine (TPMA) as a ligand. In this system, the monomer and initiating species in toluene (organic phase) and the catalyst complexes in water (aqueous phase) are simply mixed under stirring at room temperature. The trace catalyst complexes transfer into the organic phase via diffusion to trigger ICAR ATRP of MMA with ppm level catalyst content once the system is heated to the polymerization temperature (75 °C). It is found that well-defined PMMA with controlled molecular weights and narrow molecular weight distributions can be obtained easily. Furthermore, the polymerization can be conducted in the presence of limited amounts of air without using tedious degassed procedures. After cooling to room temperature, the upper organic phase is decanted and the lower aqueous phase is reused for another 10 recycling turnovers with ultra low loss of catalyst and ligand loading. At the same time, all the recycled catalyst complexes retain nearly perfect catalytic activity and controllability, indicating a facile and economical strategy for catalyst removal and recycling.

  3. Extraction and isolation of lithospermic acid B from Salvia miltiorrhiza Bunge using aqueous two-phase extraction followed by high-performance liquid chromatography.

    Science.gov (United States)

    Guo, Yong Xue; Shi, Chang Zhi; Zhang, Lei; Lv, Lin; Zhang, Yue Yong

    2016-09-01

    A rapid and effective method integrating separation and purification of lithospermic acid B from Salvia miltiorrhiza Bunge was developed by combining an aqueous two-phase system extraction with preparative chromatography. An aqueous two-phase system of n-butyl alcohol/KH2 PO4 was chosen from seven systems. The influence of parameters including concentration of KH2 PO4 , n-butyl alcohol concentration, pH, and the ratio of an aqueous two-phase system to crude extract were investigated using a single factor design. Response surface methodology was subsequently used to find the optimal compositions of an aqueous two-phase system. Keeping a solvent-to-solid ratio of 10, the final optimized composition of an aqueous two-phase system was 39.1% w/w n-butyl alcohol and 22.6% w/w KH2 PO4 . Under these conditions a recovery yield of 99.8% and a high partition coefficient of 310.4 were obtained. In a pilot-scale experiment using optimized conditions, 18.79 g of lithospermic acid B with a purity of 70.5% and in a yield of 99.8% was separated from 0.5 kg of crude extract. Subsequently, 9.94 g lithospermic acid B with a purity of 99.3% and recovery yield of 70.3% was obtained with a preparative chromatographic process, and the two-step total recovery was 70.1%. PMID:27484287

  4. Radical mechanisms of methyl vinyl ketone oligomerization through aqueous phase OH-oxidation: on the paradoxical role of dissolved molecular oxygen

    Directory of Open Access Journals (Sweden)

    P. Renard

    2013-07-01

    Full Text Available It is now accepted that one of the important pathways of secondary organic aerosol (SOA formation occurs through aqueous phase chemistry in the atmosphere. However, the chemical mechanisms leading to macromolecules are still not well understood. It was recently shown that oligomer production by OH radical oxidation in the aerosol aqueous phase from α-dicarbonyl precursors, such as methylglyoxal and glyoxal, is irreversible and fast. Methyl vinyl ketone (MVK was chosen in the present study as it is an α,β-unsaturated carbonyl that can undergo radical oligomerization in the aerosol aqueous phase. We present here experiments on the aqueous phase OH-oxidation of MVK, performed under various conditions. Using NMR and UV absorption spectroscopy, high and ultra-high resolution mass spectrometry, we show that the fast formation of oligomers up to 1800 Da is due to radical oligomerization of MVK, and 13 series of oligomers (out of a total of 26 series are identified. The influence of atmospherically relevant parameters such as temperature, initial concentrations of MVK and dissolved oxygen are presented and discussed. In agreement with the experimental observations, we propose a chemical mechanism of OH-oxidation of MVK in the aqueous phase that proceeds via radical oligomerization of MVK on the olefin part of the molecule. This mechanism highlights in our experiments the paradoxical role of dissolved O2: while it inhibits oligomerization reactions, it contributes to produce oligomerization initiator radicals, which rapidly consume O2, thus leading to the dominance of oligomerization reactions after several minutes of reaction. These processes, together with the large range of initial concentrations investigated show the fundamental role that radical oligomerization processes likely play in polluted fogs and atmospheric aerosol.

  5. 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

  6. Influence of salts on the coexistence curve and protein partitioning in nonionic aqueous two-phase micellar systems

    Directory of Open Access Journals (Sweden)

    A. M. Lopes

    2014-12-01

    Full Text Available Aqueous two-phase micellar systems (ATPMS can be exploited in separation science for the extraction/purification of desired biomolecules. Prior to phase separation the surfactant solution reaches a cloud point temperature, which is influenced by the presence of electrolytes. In this work, we provide an investigation on the cloud point behavior of the nonionic surfactant C10E4 in the presence of NaCl, Li2SO4 and KI. We also investigated the salts' influence on a model protein partitioning. NaCl and Li2SO4 promoted a depression of the cloud point. The order of salts and the concentration that decreased the cloud point was: Li2SO4 0.5 M > NaCl 0.5 M ≈ Li2SO4 0.2 M. On the other hand, 0.5 M KI dislocated the curve to higher cloud point values. For our model protein, glucose-6-phosphate dehydrogenase (G6PD, partitioning experiments with 0.5 M NaCl or 0.2 M Li2SO4 at 13.85 ºC showed similar results, with K G6PD ~ 0.46. The lowest partition coefficient was obtained in the presence of 0.5 M KI (K G6PD = 0.12, with major recovery of the enzyme in the micelle-dilute phase (%Recovery = 90%. Our results show that choosing the correct salt to add to ATPMS may be useful to attain the desired partitioning conditions at more extreme temperatures. Furthermore, this system can be effective to separate a target biomolecule from fermented broth contaminants.

  7. Extra-column dispersion of macromolecular solutes in aqueous-phase size-exclusion chromatography.

    Science.gov (United States)

    Grznárová, G; Polakovic, M; Acai, P; Görner, T

    2004-06-18

    A set of dextran standards was used to study the extra-column dispersion in conventional chromatographic equipment at a broad range of molecular weights, different mobile phase flow rates and connecting tube lengths and diameters. All known correlations for the tube dispersion at laminar flow, including those for short tubes, overestimated the values of the variance of the outlet concentration signal. The difference increased with the solute molecular weight and the flow rate. It was assumed that the discrepancy was due to the effect of natural convection invoked by the density differences of the injected dextran solutions and water. A suitable approximation of the relative band spreading was suggested in a form of a power function of the Reynolds and Schmidt numbers. A significant decrease of the dispersion was observed when the chromatography tubing was coiled into a circle. This decrease was successfully predicted combining the existing correlations for long coiled tubes and short straight tubes.

  8. Three-phase microemulsion/sol-gel system for aqueous catalysis with hydrophobic chemicals.

    Science.gov (United States)

    Abu-Reziq, Raed; Blum, Jochanan; Avnir, David

    2004-02-20

    A facile three-phase transport process is described that allows to carry out catalytic reactions in water, whereby all components are hydrophobic. According to this process a hydrophobic substrate is microemulsified in water and subjected to an organometallic catalyst, which is entrapped within a partially hydrophobized sol-gel matrix. The surfactant molecules, which carry the hydrophobic substrate, adsorb/desorb reversibly on the surface of the sol-gel matrix breaking the micellar structure, spilling their substrate load into the porous medium that contains the catalyst. A catalytic reaction then takes place within the ceramic material to form the desired products that are extracted by the desorbing surfactant, carrying the emulsified product back into the solution. The method is general and versatile and has been demonstrated with the catalytic hydrogenations of alkenes, alkynes, aromatic C=C bonds, and nitro and cyano groups.

  9. An example of transition from a corrosion process in gaseous phase to corrosion in aqueous environment: the case of Z2CN18-10 stainless steel by iodine and water in vapour phase

    International Nuclear Information System (INIS)

    This research thesis addresses an example of transition of a corrosion process in gaseous phase towards corrosion in aqueous environment, specifically in the case of the corrosion of the Z2CN18-10 stainless steel by gaseous iodine in presence of water vapour (and possibly nitrogen dioxide). This transition occurs in two steps: initiation in gaseous phase and growth in aqueous environment. This transition is due to hygroscopic properties of mostly chromium iodides and, to a lesser extent, iron iodides. Morphological, electrochemical and thermogravimetry studies have been performed by varying different parameters governing corrosion processes: corrosion temperature, iodine concentration, relative humidity, and reaction time

  10. Effect of ph value of aqueous phase on interphase tension of organic acids in the system of tri-n-butyl phosphate

    International Nuclear Information System (INIS)

    The dependence of interphase tension of extractant, usually applied for extraction reprocessing of NPP spent fuel (30% solution of tri-n-butylphosphate in n-dodecane), containing carbonic and dialkylphosphoric acids with a long alkyl chain, on the value of hydrogen index of pH of equilibrium aqueous phase is studied. The data obtained are compared with similar dependences, characteristic of extractant, which does not contain organic acid additions, as well as of extractant irradiated by 60Co γ-source with doses 108 and 432 kGy. It is shown that in irradiated organic solutions, except compounds belonging to the class of dialkylphosphoric acids, at least two more classes of organic derivatives of acid character are present, which differ in the constants of acid dissociation and result in the decrease of interphase tension in the system. Compounds belonging to the class of dialkylphosphoric acids are to a less degree responsible for the decrease in interphase tension in the system than weaker, for instance carbonic, acids. The method can be used for the indentification of different classes of aniongenic surfactants in radiation-affected extraction systems

  11. One-step and rapid synthesis of high quality alloyed quantum dots (CdSe-CdS) in aqueous phase by microwave irradiation with controllable temperature

    International Nuclear Information System (INIS)

    In this paper, we presented a seed-mediated approach for rapid synthesis of high quality alloyed quantum dots (CdSe-CdS) in aqueous phase by microwave irradiation with controllable temperature in 1 h. In the synthesis, CdSe seeds were first formed by the reaction of NaHSe and Cd2+, and then alloyed quantum dots (CdSe-CdS) were rapidly produced by releasing of sulfide ions from 3-mercaptopropionic acid as sulfide source with microwave irradiation. The alloyed quantum dots synthesized had good optical properties, the quantum yield was up to 25%, and the full width at half maximum of the emission spectrum peak was about 28 nm. The as-prepared alloyed CdSe-CdS QDs were characterized by XRD, XPS and ICP-AES in order to explore the structure and component of the alloyed nanocrystals and the reaction mechanism. We speculate that the alloyed CdSe-CdS quantum dots may exist a gradient internal structure according to our preliminary results

  12. A Complex Matrix Factorization approach to Joint Modeling of Magnitude and Phase for Source Separation

    OpenAIRE

    Ahuja, Chaitanya; Nathwani, Karan; Rajesh M. Hegde

    2014-01-01

    Conventional NMF methods for source separation factorize the matrix of spectral magnitudes. Spectral Phase is not included in the decomposition process of these methods. However, phase of the speech mixture is generally used in reconstructing the target speech signal. This results in undesired traces of interfering sources in the target signal. In this paper the spectral phase is incorporated in the decomposition process itself. Additionally, the complex matrix factorization problem is reduce...

  13. Sulfur isotope fractionation during oxidation of sulfur dioxide: gas-phase oxidation by OH radicals and aqueous oxidation by H2O2, O3 and iron catalysis

    Directory of Open Access Journals (Sweden)

    J. N. Crowley

    2012-01-01

    Full Text Available The oxidation of SO2 to sulfate is a key reaction in determining the role of sulfate in the environment through its effect on aerosol size distribution and composition. Sulfur isotope analysis has been used to investigate sources and chemical processes of sulfur dioxide and sulfate in the atmosphere, however interpretation of measured sulfur isotope ratios is challenging due to a lack of reliable information on the isotopic fractionation involved in major transformation pathways. This paper presents laboratory measurements of the fractionation factors for the major atmospheric oxidation reactions for SO2: Gas-phase oxidation by OH radicals, and aqueous oxidation by H2O2, O3 and a radical chain reaction initiated by iron. The measured fractionation factor for 34S/32S during the gas-phase reaction is αOH = (1.0089±0.0007−((4±5×10−5 T(°C. The measured fractionation factor for 34S/32S during aqueous oxidation by H2O2 or O3 is αaq = (1.0167±0.0019−((8.7±3.5 ×10−5T(°C. The observed fractionation during oxidation by H2O2 and O3 appeared to be controlled primarily by protonation and acid-base equilibria of S(IV in solution, which is the reason that there is no significant difference between the fractionation produced by the two oxidants within the experimental error. The isotopic fractionation factor from a radical chain reaction in solution catalysed by iron is αFe = (0.9894±0.0043 at 19 °C for 34S/32S. Fractionation was mass-dependent with regards to 33S/32S for all the reactions investigated. The radical chain reaction mechanism was the only measured reaction that had a faster rate for the light isotopes. The results presented in this study will be particularly useful to determine the importance of the transition metal-catalysed oxidation pathway compared to other oxidation pathways, but other main oxidation pathways can not be distinguished based on stable sulfur isotope measurements alone.

  14. Recovery of ascorbic oxidoreductase from crude extract with an aqueous two-phase system in a perforated rotating disc contactor

    Directory of Open Access Journals (Sweden)

    Ana Lúcia Figueiredo Porto

    2004-09-01

    Full Text Available A continuous perforated rotating disc contactor was used to extract the enzyme ascorbic oxidoreductase (E.C.1.10.3.3 from crude extract of Curcubita maxima with an aqueous two-phase system of poly (ethylene glycol and phosphate salts. The effect of dispersed phase velocity on either protein mass transfer coefficients or separation efficiency at 1, 2 and 3 mL/min was studied. An increase of the mass transfer coefficients was observed with the dispersed phase velocity, while the separation efficiency showed a small decrease with the increase of this parameter. The experimental results obtained during continuous extraction showed that the ascorbic oxidoreductase activity was partitioned preferentially into the salt-rich phase in all conditions studied. The best recovery of enzyme activity was 236%, with a purification factor of 34 in flow rates of 1 mL/min for dispersed phase.Uma coluna de discos perfurados rotativos foi utilizada na extração da enzima ascorbato oxidorredutase (E.C.1.10.3.3, obtida do extrato bruto de Curcubita maxima, através da utilização do sistema bifásico aquoso Polietilenoglicol-sais de fosfato. Os efeitos da velocidade da fase dispersa nos coeficientes de transferência de massa e na eficiência de separação para valores de 1, 2 e 3 mL/min foram estudados. Observou-se um aumento da transferência de massa com a velocidade da fase dispersa, enquanto que a eficiência de separação demonstrou uma ligeira redução com o aumento deste parâmetro. Os resultados experimentais obtidos durante a extração contínua demonstraram que a atividade da ascorbato oxidorredutase se concentrou preferencialmente na fase rica em sal para todas as condições estudadas. A maior recuperação da atividade enzimática foi de 236%, com um fator de purificação de 34 para o valor de 1 mL/min para a fase dispersa.

  15. Countercurrent Chromatographic Separation of Lipophilic Ascorbic Acid Derivatives and Extract from Kadsura Coccinea Using Hydrophobic Organic-Aqueous Two-Phase Solvent Systems

    OpenAIRE

    Shinomiya, Kazufusa; Li, Heran; Kitanaka, Susumu; Ito, Yoichiro

    2009-01-01

    Countercurrent chromatographic (CCC) separation of lipophilic ascorbic acid derivatives and the crude extract from Kadsura Coccinea was performed using the type-J multilayer coil planet centrifuge with a hydrophobic organic-aqueous two-phase solvent system composed of n-hexane/ethyl acetate/ethanol/aqueous 0.1% trifluoroacetic acid at the volume ratio of (5 : 5 : 6 : 2). The lipophilic ascorbic acid derivatives were separated in the order of L-ascrobyl 2,6-dibutyrate, L-ascorbyl 6-palmitate a...

  16. Dissolution of metal oxides in an acid-saturated ionic liquid solution and investigation of the back-extraction behaviour to the aqueous phase

    OpenAIRE

    Wellens, Sil; Vander Hoogerstraete, Tom; Möller, Claudia; Thijs, Ben; Luyten, Jan; Binnemans, Koen

    2014-01-01

    The dissolution of metal oxides in an acid-saturated ionic liquid, followed by selective stripping of the dissolved metal ions to an aqueous phase is proposed as a new ionometallurgical approach for the processing of metals in ionic liquids. The hydrophobic ionic liquid trihexyl(tetradecyl)phosphonium chloride (Cyphos IL 101) saturated with a concentrated aqueous hydrochloric acid solution was used to dissolve CaO, NiO, MnO, CoO, CuO, ZnO and Fe2O3. It was found that nickel(II) and calcium...

  17. Effects of HCl and HNO3 on the oxidation of toluene to benzaldehyde by H2O2 over TS-1 modified with Al in aqueous phase

    Directory of Open Access Journals (Sweden)

    Paricha Pongjirawat

    2014-09-01

    Full Text Available This research studies effects of HCl and HNO3 in aqueous solution on the oxidation reaction between toluene and hydrogen peroxide to benzaldehyde over titanium silicalite-1 catalyst modified with Al. The reaction was carried out at reaction temperature 120°C in a pressurized autoclave reactor. The research found that the addition of HCl and HNO3 not only increases the concentration of toluene in the aqueous phase but also increases the formation of benzaldehyde as main product in the reaction.

  18. DISTRIBUTION OF ACTINIDES BETWEEN THE AQUEOUS AND ORGANIC PHASES IN THE TALSPEAK PROCESS

    Energy Technology Data Exchange (ETDEWEB)

    Rudisill, T.; Kyser, E.

    2010-09-02

    One objective of the US Department of Energy's Office of Nuclear Energy (DOE-NE) is the development of sustainable nuclear fuel cycles which improve uranium resource utilization, maximize energy generation, minimize waste generation, improve safety, and complement institutional measures limiting proliferation risks. Activities in progress which support this objective include the development of advanced separation technologies to recover the actinides from used nuclear fuels. With the increased interest in the development of technology to allow closure of the nuclear fuel cycle, the TALSPEAK process is being considered for the separation of Am and Cm from the lanthanide fission products in a next generation reprocessing plant. However, at this time, the level of understanding associated with the chemistry and the control of the process variables is not acceptable for deployment of the process on an industrial scale. To address this issue, DOE-NE is supporting basic scientific studies focused on the TALSPEAK process through its Fuel Cycle Research and Development (R&D) program. One aspect of these studies is an experimental program at the Savannah River National Laboratory (SRNL) in which temperature-dependent distribution coefficients for the extraction of actinide elements in the TALSPEAK process were measured. The data were subsequently used to calculate conditional enthalpies and entropies of extraction by van't Hoff analysis to better understand the thermodynamic driving forces for the TALSPEAK process. In the SRNL studies, the distribution of Pu(III) in the TALSPEAK process was of particular interest. A small amount of Pu(III) would be present in the feed due to process losses and valence adjustment in prior recovery operations. Actinide elements such as Np and Pu have multiple stable oxidation states in aqueous solutions; therefore the oxidation state for these elements must be controlled in the TALSPEAK process, as the extraction chemistry is

  19. Phase 1 report: investigation of geothermal energy information sources

    Energy Technology Data Exchange (ETDEWEB)

    1976-07-14

    A subject screening list was developed which would be used by acquisitions specialists as a guide to the orientation of pertinent literature. The subject screening list was derived primarily from the geothermal subset of the ERDA Energy Thesaurus and from the ERDA Energy Information Data Base Subject Categories (TID-4584). The subject screening list is included. Subsequent to preparation of the subject screening list, a core list of serial publications containing geothermal energy information was generated by SIS library scientists. This list was corelated with the ERDA-TIC serial publications list. Included in both lists is an estimate of the annual geothermal information yield of the serial sources. A listing of sources of geothermal energy information other than serial publications and the conclusions, including methods of acquisitioning to be utilized and the estimated annual volume of information from all sources are presented.

  20. Abiotic degradation of four phthalic acid esters in aqueous phase under natural sunlight irradiation

    Institute of Scientific and Technical Information of China (English)

    Ruttapol Lertsirisopon; Satoshi Soda; Kazunari Sei; Michihiko Ike

    2009-01-01

    Abiotic degradability of four phthalic acid esters (PAEs) in the aquatic phase was evaluated over the wide pH range (5-9). The PAE solutions in glass test tubes were placed in the dark and under natural sunlight irradiation for evaluating the degradation rate via hydrolysis and photolysis plus hydrolysis, respectively, at ambient temperature for 140 d from autumn to winter in Osaka, Japan. The efficiency of abiotic degradation of the PAEs with relatively short alkyl chain, butylbenzyl phthalate (BBP) and di-n-butyl phthalate (DBP) at neutral pH was significant less than that in the acidic or alkaline condition. Photolysis was considered to mainly contribute to total abiotic degradation at any pH. Neither hydrolysis nor photolysis of di-ethylhexyl phthalate (DEHP) proceeded significantly at any pH, especially hydrolysis at neutral pH was negligible. On the other hand, the degradation rate of di-isononyl phthalate (DINP) mainly catalyzed by photolysis was much higher compared with that of the other PAEs, and almost complete removal was observed during the experimental period at pH 5.0 and 9.0. As a whole, according to the half-life (t1/2) obtained in the experiments, the abiotic degradability of the PAEs was in the sequence, DINP (32-140 d) > DBP (50-360 d), BBP (58-480 d) > DEHP (390-1600 d) under sunlight irradiation (via photolysis plus hydrolysis). Although the abiotic degradation rate for BBP, DBP, and DEHP are much lower than their biodegradation rate reported, the photolysis rate for DINP is comparable to its biodegradation rate in the acidic or alkaline condition.

  1. Design and comparison of three-level three-phase T-source inverters

    DEFF Research Database (Denmark)

    Shults, T.; Husev, Oleksandr; Blaabjerg, Frede

    2015-01-01

    This paper presents guidelines for component design of recently proposed topologies of the three-level three-phase T-source inverters. Two different topologies are considered: T-source inverters with discontinuous input current and T-source inverters with continuous input current. Steady state...

  2. A new source discriminant based on frequency dispersion for hydroacoustic phases recorded by T-phase stations

    Science.gov (United States)

    Talandier, Jacques; Okal, Emile A.

    2016-07-01

    In the context of the verification of the Comprehensive Nuclear-Test Ban Treaty in the marine environment, we present a new discriminant based on the empirical observation that hydroacoustic phases recorded at T-phase stations from explosive sources in the water column feature a systematic inverse dispersion, with lower frequencies traveling slower, which is absent from signals emanating from earthquake sources. This difference is present even in the case of the so-called "hotspot earthquakes" occurring inside volcanic edifices featuring steep slopes leading to efficient seismic-acoustic conversions, which can lead to misidentification of such events as explosions when using more classical duration-amplitude discriminants. We propose an algorithm for the compensation of the effect of dispersion over the hydroacoustic path based on a correction to the spectral phase of the ground velocity recorded by the T-phase station, computed individually from the dispersion observed on each record. We show that the application of a standard amplitude-duration algorithm to the resulting compensated time series satisfactorily identifies records from hotspot earthquakes as generated by dislocation sources, and present a full algorithm, lending itself to automation, for the discrimination of explosive and earthquake sources of hydroacoustic signals at T-phase stations. The only sources not readily identifiable consist of a handful of complex explosions which occurred in the 1970s, believed to involve the testing of advanced weaponry, and which should be independently identifiable through routine vetting by analysts. While we presently cannot provide a theoretical justification to the observation that only explosive sources generate dispersed T phases, we hint that this probably reflects a simpler, and more coherent distribution of acoustic energy among the various modes constituting the wavetrain, than in the case of dislocation sources embedded in the solid Earth.

  3. A new source discriminant based on frequency dispersion for hydroacoustic phases recorded by T-phase stations

    Science.gov (United States)

    Talandier, Jacques; Okal, Emile A.

    2016-09-01

    In the context of the verification of the Comprehensive Nuclear-Test Ban Treaty in the marine environment, we present a new discriminant based on the empirical observation that hydroacoustic phases recorded at T-phase stations from explosive sources in the water column feature a systematic inverse dispersion, with lower frequencies traveling slower, which is absent from signals emanating from earthquake sources. This difference is present even in the case of the so-called `hotspot earthquakes' occurring inside volcanic edifices featuring steep slopes leading to efficient seismic-acoustic conversions, which can lead to misidentification of such events as explosions when using more classical duration-amplitude discriminants. We propose an algorithm for the compensation of the effect of dispersion over the hydroacoustic path based on a correction to the spectral phase of the ground velocity recorded by the T-phase station, computed individually from the dispersion observed on each record. We show that the application of a standard amplitude-duration algorithm to the resulting compensated time-series satisfactorily identifies records from hotspot earthquakes as generated by dislocation sources, and present a full algorithm, lending itself to automation, for the discrimination of explosive and earthquake sources of hydroacoustic signals at T-phase stations. The only sources not readily identifiable consist of a handful of complex explosions which occurred in the 1970s, believed to involve the testing of advanced weaponry, and which should be independently identifiable through routine vetting by analysts. While we presently cannot provide a theoretical justification to the observation that only explosive sources generate dispersed T phases, we hint that this probably reflects a simpler, and more coherent distribution of acoustic energy among the various modes constituting the wave train, than in the case of dislocation sources embedded in the solid Earth.

  4. Optimization of Serine Protease Purification from Mango (Mangifera indica cv. Chokanan Peel in Polyethylene Glycol/Dextran Aqueous Two Phase System

    Directory of Open Access Journals (Sweden)

    Abdul Manap Mohd Yazid

    2012-03-01

    Full Text Available Mango peel is a good source of protease but remains an industrial waste. This study focuses on the optimization of polyethylene glycol (PEG/dextran-based aqueous two-phase system (ATPS to purify serine protease from mango peel. The activity of serine protease in different phase systems was studied and then the possible relationship between the purification variables, namely polyethylene glycol molecular weight (PEG, 4000–12,000 g·mol−1, tie line length (−3.42–35.27%, NaCl (−2.5–11.5% and pH (4.5–10.5 on the enzymatic properties of purified enzyme was investigated. The most significant effect of PEG was on the efficiency of serine protease purification. Also, there was a significant increase in the partition coefficient with the addition of 4.5% of NaCl to the system. This could be due to the high hydrophobicity of serine protease compared to protein contaminates. The optimum conditions to achieve high partition coefficient (84.2 purification factor (14.37 and yield (97.3% of serine protease were obtained in the presence of 8000 g·mol−1 of PEG, 17.2% of tie line length and 4.5% of NaCl at pH 7.5. The enzymatic properties of purified serine protease using PEG/dextran ATPS showed that the enzyme could be purified at a high purification factor and yield with easy scale-up and fast processing.

  5. Valorisation of Vietnamese Rice Straw Waste: Catalytic Aqueous Phase Reforming of Hydrolysate from Steam Explosion to Platform Chemicals

    Directory of Open Access Journals (Sweden)

    Cao Huong Giang

    2014-12-01

    Full Text Available A family of tungstated zirconia solid acid catalysts were synthesised via wet impregnation and subsequent thermochemical processing for the transformation of glucose to 5-hydroxymethylfurfural (HMF. Acid strength increased with tungsten loading and calcination temperature, associated with stabilisation of tetragonal zirconia. High tungsten dispersions of between 2 and 7 W atoms·nm−2 were obtained in all cases, equating to sub-monolayer coverages. Glucose isomerisation and subsequent dehydration via fructose to HMF increased with W loading and calcination temperature up to 600 °C, indicating that glucose conversion to fructose was favoured over weak Lewis acid and/or base sites associated with the zirconia support, while fructose dehydration and HMF formation was favoured over Brönsted acidic WOx clusters. Aqueous phase reforming of steam exploded rice straw hydrolysate and condensate was explored heterogeneously for the first time over a 10 wt% WZ catalyst, resulting in excellent HMF yields as high as 15% under mild reaction conditions.

  6. Partitioning of chloroaromatic compounds between the aqueous phase and dissolved and particulate soil organic matter at chlorophenol contaminated sites

    Energy Technology Data Exchange (ETDEWEB)

    Frankki, Sofia [Department of Forest Ecology, Swedish University of Agricultural Sciences, SE-901 83 Umea (Sweden); Persson, Ylva [Environmental Chemistry, Department of Chemistry, Umea University, SE-901 87 Umea (Sweden); Shchukarev, Andrei [Inorganic Chemistry, Department of Chemistry, Umea University, SE-901 87 Umea (Sweden); Tysklind, Mats [Environmental Chemistry, Department of Chemistry, Umea University, SE-901 87 Umea (Sweden); Skyllberg, Ulf [Department of Forest Ecology, Swedish University of Agricultural Sciences, SE-901 83 Umea (Sweden)]. E-mail: ulf.skyllberg@sek.slu.se

    2007-07-15

    The retention and mobility of hydrophobic organic contaminants (HOCs) in soil is mainly determined by hydrophobic partitioning to dissolved and particulate organic matter (DOM and POM, respectively). The aqueous phase, DOM, and POM fractions were extracted and separated from soils at three sites contaminated with technical chlorophenol formulations. Concentrations of chlorophenols (CP), polychlorinated phenoxyphenols (PCPP), polychlorinated diphenyl ethers (PCDE) and polychlorinated dibenzo-p-dioxins and furans (PCDD/F) were determined. The partitioning to POM, in relation to DOM, increased in all three soils with increasing hydrophobicity in the order CP < PCPP {approx} PCDE {approx} PCDF < PCDD. Differences in partitioning to DOM (log K {sub DOC}) and POM (log K {sub POC}) could not be explained by differences in gross organic C chemistry. Black carbon did not contribute significantly to the sorption of PCDDs, whereas >70% wood fibre in one soil resulted in a decrease of log K {sub POC} of 0.5 units for CPs and PCDDs. We conclude that log K {sub OC} for both DOM and POM need to be explicitly determined when the retention and mobility of HOCs is described and modelled in soils. - Increasing hydrophobicity of organic compounds increases the partitioning to particulate natural organic matter relative to dissolved natural organic matter.

  7. Carbon-coated ceramic membrane reactor for the production of hydrogen by aqueous-phase reforming of sorbitol.

    Science.gov (United States)

    Neira D'Angelo, M F; Ordomsky, V; Schouten, J C; van der Schaaf, J; Nijhuis, T A

    2014-07-01

    Hydrogen was produced by aqueous-phase reforming (APR) of sorbitol in a carbon-on-alumina tubular membrane reactor (4 nm pore size, 7 cm long, 3 mm internal diameter) that allows the hydrogen gas to permeate to the shell side, whereas the liquid remains in the tube side. The hydrophobic nature of the membrane serves to avoid water loss and to minimize the interaction between the ceramic support and water, thus reducing the risks of membrane degradation upon operation. The permeation of hydrogen is dominated by the diffusivity of the hydrogen in water. Thus, higher operation temperatures result in an increase of the flux of hydrogen. The differential pressure has a negative effect on the flux of hydrogen due to the presence of liquid in the larger pores. The membrane was suitable for use in APR, and yielded 2.5 times more hydrogen than a reference reactor (with no membrane). Removal of hydrogen through the membrane assists in the reaction by preventing its consumption in undesired reactions.

  8. 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.

  9. 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

  10. Partitioning of chloroaromatic compounds between the aqueous phase and dissolved and particulate soil organic matter at chlorophenol contaminated sites

    International Nuclear Information System (INIS)

    The retention and mobility of hydrophobic organic contaminants (HOCs) in soil is mainly determined by hydrophobic partitioning to dissolved and particulate organic matter (DOM and POM, respectively). The aqueous phase, DOM, and POM fractions were extracted and separated from soils at three sites contaminated with technical chlorophenol formulations. Concentrations of chlorophenols (CP), polychlorinated phenoxyphenols (PCPP), polychlorinated diphenyl ethers (PCDE) and polychlorinated dibenzo-p-dioxins and furans (PCDD/F) were determined. The partitioning to POM, in relation to DOM, increased in all three soils with increasing hydrophobicity in the order CP DOC) and POM (log K POC) could not be explained by differences in gross organic C chemistry. Black carbon did not contribute significantly to the sorption of PCDDs, whereas >70% wood fibre in one soil resulted in a decrease of log K POC of 0.5 units for CPs and PCDDs. We conclude that log K OC for both DOM and POM need to be explicitly determined when the retention and mobility of HOCs is described and modelled in soils. - Increasing hydrophobicity of organic compounds increases the partitioning to particulate natural organic matter relative to dissolved natural organic matter

  11. Phase Behavior of Aqueous NA-K-MG-CA-CI-NO3 Mixtures: Isopiestic Measurements and Thermodynamic Modeling

    Energy Technology Data Exchange (ETDEWEB)

    M.S. Gruszkiewiez; D.A. Palmer; R.D. Springer; P. Wang; A. Anderko

    2006-09-14

    A comprehensive model has been established for calculating thermodynamic properties of multicomponent aqueous systems containing the Na{sup +}, K{sup +}, Mg{sup 2+}, Ca{sup 2+}, Cl{sup -}, and NO{sub 3}{sup -} ions. The thermodynamic framework is based on a previously developed model for mixed-solvent electrolyte solutions. The framework has been designed to reproduce the properties of salt solutions at temperatures ranging from the freezing point to 300 C and concentrations ranging from infinite dilution to the fused salt limit. The model has been parameterized using a combination of an extensive literature database and new isopiestic measurements for thirteen salt mixtures at 140 C. The measurements have been performed using Oak Ridge National Laboratory's (ORNL) previously designed gravimetric isopiestic apparatus, which makes it possible to detect solid phase precipitation. Water activities are reported for mixtures with a fixed ratio of salts as a function of the total apparent salt mole fraction. The isopiestic measurements reported here simultaneously reflect two fundamental properties of the system, i.e., the activity of water as a function of solution concentration and the occurrence of solid-liquid transitions. The thermodynamic model accurately reproduces the new isopiestic data as well as literature data for binary, ternary and higher-order subsystems. Because of its high accuracy in calculating vapor-liquid and solid-liquid equilibria, the model is suitable for studying deliquescence behavior of multicomponent salt systems.

  12. Radiolysis of C5-BTBP in cyclohexanone irradiated in the absence and presence of an aqueous phase

    Energy Technology Data Exchange (ETDEWEB)

    Fermvik, A.; Aneheim, E.; Kvicalova, M.; Ekberg, C. [Chalmers Univ. of Technology, Goeteborg (Sweden). Nuclear Chemistry; Chalmers Univ. of Technology, Goeteborg (Sweden). Industrial Materials Recycling; Gruener, B.; Hajkova, Z. [Academy of Sciences of the Czech Republic, Husinec-Rez (Czech Republic). Inst. of Inorganic Chemistry

    2012-07-01

    Spent nuclear fuel contains many highly radioactive species; hence solvents used in reprocessing will be subjected to radiolysis. In this study, solvents containing one of the BTBP molecules intended for the separation of trivalent actinides and lanthanides, the so called C5-BTBP, have been subjected to radiolysis and hydrolysis. We present here that this compound shows a dramatic decrease in both distribution ratios and separation factor when irradiated with higher doses up to 50 kGy; particularly in the presence of an aqueous phase. Furthermore, fast hydrolytic degradation is observed, which significantly contributes to the overall degree of decomposition. This is supported by speciation studies performed by HPLC and LC-MS methods. Proposed structures of the highest-yield degradation products are presented and they seem to confirm previously drawn structures for these products. From these studies it can be concluded that the presence of nitric acid or nitrate during irradiation leads to higher content of species containing keto groups. (orig.)

  13. Correlation of the heterogeneous discoloration efficiency of aqueous Rhodamine-B solutions and charge separation enhancement of mixed-phase nanocrystalline titania

    Science.gov (United States)

    Zhang, Dongfang

    2012-05-01

    Heterogeneous photocatalytic removal of Rhodamine-B (RhB) dye from liquid phase was done using mixed-phase nanocrystalline TiO2 for enhancement of charge separation and UV-visible-light-driven photocatalysis capabilities. The mixed-phase nanocrystalline TiO2 was characterized using various analytical techniques including XRD, TEM, UV-vis DRS and PL to investigate its phase composition and structure, nanocrystalline size distribution, band gap energy, and photoluminescence properties. The photocatalytic discoloration efficiency of mixed-phase nanocrystalline titania was explored by monitoring the decomposition of RhB dye in an aqueous solution. The results showed that the as-prepared mixed-phase nanocrystalline TiO2 was excellent for degradation of RhB molecule, and the combination of crystal phase of anatase and rutile has great effect on decomposition of RhB. The kinetic studies demonstrate that the photocatalytic oxidation reaction followed a pseudo-first-order expression due to the evidence of linear correlation between ln( c/c 0) vs. reaction time t. Moreover, the aqueous RhB dye decomposition over the as-prepared mixed-phase nanocrystalline TiO2 catalyst is controlled by RhB pre-adsorption.

  14. Preparation of Plutonium Counting Source Using Solid Phase Extraction Disk

    Institute of Scientific and Technical Information of China (English)

    SUN; Hong-qing; YANG; Su-liang; DING; You-qian; YANG; Jin-ling; MAO; Guo-shu

    2013-01-01

    For the determination of trace amount of plutonium,Pu(Ⅳ)may be extracted from dilute nitric acid by TTA-xylene,and stripped by concentrated nitric acid.But the small volume of strip solution used in traditional counting source preparation by direct evaporation could lead to a rather high detection limit.Plutonium in strip solution may all be absorbed on the surface of an anion exchange resin disk.And

  15. Polarity, selectivity and performance of hydrophilic organic/salt-containing aqueous two-phase system on counter-current chromatography for polar compounds.

    Science.gov (United States)

    Liu, Dan; Hong, Zhilai; Gao, Mingzhe; Wang, Zhixin; Gu, Ming; Zhang, Xiaozhe; Xiao, Hongbin

    2016-05-27

    The essential attributes of a solvent system for separation polar compounds on CCC are polarity, selectively and performance. Here, hydrophilic organic/salt-containing aqueous two-phase system (HO/S TPS) was evaluated as an alternative solvent system for CCC separation of polar compounds. Polarity measurements based on Rohrschneider-Snyder parameter was developed as quantitative assessing the polarity of HO/S TPS and comparing with an organic/aqueous system. All investigated 1-butanol/ethanol/saturated ammonium sulfate solution/water (BEAsWat) and 1-butanol/ethanol/saturated dipotassium hydrogen phosphate solution/water (BEDhpWat) systems with polarity values of organic phase from 4.5 to 6.8, were more polar than chloroform/methanol/water (1/1/1). The considerable water content of BEAsWat and BEDhpWat (0/1/1/1/) was 45.4 and 42.6% (w%) of hydrophilic organic phase, and 66.4 and 51.2% (w%) of salt-containing aqueous phase, respectively, closed to conventional aqueous two-phase system. Therefore, the polarity of HO/S TPS is in the middle of organic/aqueous and aqueous two-phase system. The LogKC values of twenty four polar compounds as model mixture confirmed that the polarities of HO/S TPSs were matched to that of the polar compounds and shown to be a very selective technique capable of separating positional isomers. Moreover, BEAsWat and BEDhpWat systems can be easily retained in CCC column with suitable elution mode. The hydrodynamic behavior reversion of HO/S TPS on hydrodynamic CCC was observed and was tentatively explained based on the density difference. Finally, caffeoylquinic acid isomers and dihydroxybenzoic acid isomers were successfully separated with HO/S TPS on CCC, respectively. Those results demonstrate that HO/S TPS on CCC is a performant and stable way to separate polar compounds from natural products.

  16. Radical mechanisms of methyl vinyl ketone oligomerization through aqueous phase OH-oxidation: on the paradoxical role of dissolved molecular oxygen

    Directory of Open Access Journals (Sweden)

    P. Renard

    2013-01-01

    Full Text Available It is now accepted that one of the important pathways of Secondary Organic Aerosol (SOA formation occurs through aqueous phase chemistry in the atmosphere. However, the liquid phase chemical mechanisms leading to macromolecules are still not well understood. For α-dicarbonyl precursors, such as methylglyoxal and glyoxal, radical reactions through OH-oxidation produce oligomers, irreversibly and faster than accretion reactions. Methyl vinyl ketone (MVK was chosen in the present study as it is an α, β-unsaturated carbonyl that can undergo such reaction pathways in the aqueous phase and forms even high molecular weight oligomers. We present here experiments on the aqueous phase OH-oxidation of MVK, performed under atmospheric relevant conditions. Using NMR and UV absorption spectroscopy, high and ultra-high resolution mass spectrometry, we show that the fast formation of oligomers up to 1800 Da is due to radical oligomerization of MVK, and 13 series of oligomers (out of a total of 26 series are identified. The influence of atmospherically relevant parameters such as temperature, initial concentrations of MVK and dissolved oxygen are presented and discussed. In agreement with the experimental observations, we propose a chemical mechanism of OH-oxidation of MVK in the aqueous phase that proceeds via radical oligomerization of MVK on the olefin part of the molecule. This mechanism highlights the paradoxical role of dissolved O2: while it inhibits oligomerization reactions, it contributes to produce oligomerization initiator radicals, which rapidly consume O2, thus leading to the supremacy of oligomerization reactions after several minutes of reaction. These processes, together with the large ranges of initial concentrations investigated (60–656 μM of dissolved O2 and 0.2–20 mM of MVK show the fundamental role that O2 likely plays in atmospheric organic aerosol.

  17. Spectral aspects of the determination of Si in organic and aqueous solutions using high-resolution continuum source or line source flame atomic absorption spectrometry

    Science.gov (United States)

    Kowalewska, Zofia; Pilarczyk, Janusz; Gościniak, Łukasz

    2016-06-01

    High-resolution continuum source flame atomic absorption spectrometry (HR-CS FAAS) was applied to reveal and investigate spectral interference in the determination of Si. An intensive structured background was observed in the analysis of both aqueous and xylene solutions containing S compounds. This background was attributed to absorption by the CS molecule formed in the N2O-C2H2 flame. The lines of the CS spectrum at least partially overlap all five of the most sensitive Si lines investigated. The 251.611 nm Si line was demonstrated to be the most advantageous. The intensity of the structured background caused by the CS molecule significantly depends on the chemical form of S in the solution and is the highest for the most-volatile CS2. The presence of O atoms in an initial S molecule can diminish the formation of CS. To overcome this S effect, various modes of baseline fitting and background correction were evaluated, including iterative background correction (IBC) and utilization of correction pixels (WRC). These modes were used either independently or in conjunction with least squares background correction (LSBC). The IBC + LSBC mode can correct the extremely strong interference caused by CS2 at an S concentration of 5% w:w in the investigated solution. However, the efficiency of this mode depends on the similarity of the processed spectra and the correction spectra in terms of intensity and in additional effects, such as a sloping baseline. In the vicinity of the Si line, three lines of V were recorded. These lines are well-separated in the HR-CS FAAS spectrum, but they could be a potential source of overcorrection when using line source flame atomic absorption spectrometry (LS FAAS). The expected signal for the 251.625 nm Fe line was not registered at 200 mg L- 1 Fe concentration in the solution, probably due to the diminished population of Fe atoms in the high-temperature flame used. The observations made using HR-CS FAAS helped to establish a "safe" level

  18. General-purpose heat source development. Phase II: conceptual designs

    International Nuclear Information System (INIS)

    Basic geometric module shapes and fuel arrays were studied to determine how well they could be expected to meet the General Purpose Heat Source (GPHS) design requirements. Seven conceptual designs were selected, detailed drawings produced, and these seven concepts analyzed. Three of these design concepts were selected as GPHS Trial Designs to be reanalyzed in more detail and tested. The geometric studies leading to the selection of the seven conceptual designs, the analyses of these designs, and the selection of the three trial designs are discussed

  19. Grating-based X-ray phase contrast imaging using polychromatic laboratory sources

    International Nuclear Information System (INIS)

    Research highlights: → Efficient use of polychromatic laboratory sources for X-ray phase contrast imaging. → The inter-grating distance is not limited by the polychromaticity of the X-ray source. → Sensitivity for phase measurements can be further improved. → Potential optimizations of the imaging system from an application perspective. - Abstract: X-ray phase contrast imaging has been demonstrated to have an improved contrast over conventional absorption imaging for those weakly absorbing objects. However, most of the hard X-ray phase-sensitive imaging has so far been impractical with laboratory available X-ray sources. Grating-based phase imaging approach has the prominent advantage that polychromatic laboratory X-ray generators can be efficiently used in a Talbot-Lau configuration. Through numerical simulations, we demonstrate here the efficient use of polychromatic X-ray laboratory sources for differential phase contrast imaging. The presented results explain why in recently reported experiments, polychromatic X-ray tubes could be efficiently used in a Talbot-Lau interferometer. Furthermore, the results indicate that the fractional Talbot distance is not limited by the polychromaticity of the X-ray source. Since the sensitivity of phase measurements is proportional to the fractional Talbot distance, the image quality for phase measurements can be further improved. Finally, the potential optimizations of the imaging system are discussed from an application perspective, taking into consideration both available X-ray flux and compactness of the system.

  20. Grating-based X-ray phase contrast imaging using polychromatic laboratory sources

    Energy Technology Data Exchange (ETDEWEB)

    Wang Zhili [Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); Gao Kun [National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230026 (China); Zhu Peiping; Yuan Qingxi; Huang Wanxia; Zhang Kai; Hong Youli [Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); Ge Xin [National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230026 (China); Wu Ziyu, E-mail: wuzy@ustc.edu.cn [Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230026 (China)

    2011-04-15

    Research highlights: {yields} Efficient use of polychromatic laboratory sources for X-ray phase contrast imaging. {yields} The inter-grating distance is not limited by the polychromaticity of the X-ray source. {yields} Sensitivity for phase measurements can be further improved. {yields} Potential optimizations of the imaging system from an application perspective. - Abstract: X-ray phase contrast imaging has been demonstrated to have an improved contrast over conventional absorption imaging for those weakly absorbing objects. However, most of the hard X-ray phase-sensitive imaging has so far been impractical with laboratory available X-ray sources. Grating-based phase imaging approach has the prominent advantage that polychromatic laboratory X-ray generators can be efficiently used in a Talbot-Lau configuration. Through numerical simulations, we demonstrate here the efficient use of polychromatic X-ray laboratory sources for differential phase contrast imaging. The presented results explain why in recently reported experiments, polychromatic X-ray tubes could be efficiently used in a Talbot-Lau interferometer. Furthermore, the results indicate that the fractional Talbot distance is not limited by the polychromaticity of the X-ray source. Since the sensitivity of phase measurements is proportional to the fractional Talbot distance, the image quality for phase measurements can be further improved. Finally, the potential optimizations of the imaging system are discussed from an application perspective, taking into consideration both available X-ray flux and compactness of the system.

  1. Theoretical considerations for X-ray phase contrast mammography by Thomson source

    Energy Technology Data Exchange (ETDEWEB)

    Cedola, A. [Istituto di Fotonica e Nanotecnologie-Consiglio Nazionale delle Ricerche (IFN-CNR), via Cineto Romano 42, I-00156 Roma (Italy); INFN, Sezione di Roma1, Piazzale Aldo Moro2, 00185 Rome (Italy)], E-mail: cedola@ifn.cnr.it; Bukreeva, I.; Lagomarsino, S. [Istituto di Fotonica e Nanotecnologie-Consiglio Nazionale delle Ricerche (IFN-CNR), via Cineto Romano 42, I-00156 Roma (Italy); INFN, Sezione di Roma1, Piazzale Aldo Moro2, 00185 Rome (Italy); Petrillo, V.; Maroli, C. [Universita di Milano, Physics Department and INFN Sezione di Milano Via Celoria 16, 20133 Milano (Italy)

    2009-09-01

    The advent, in the near future, of compact X-ray sources like Thomson Back-Scattering (TBS) will allow the clinical application of advanced X-ray imaging techniques, such as phase contrast, with higher sensitivity and lower impact in terms of dose delivery. In this work, we theoretically investigated the possibility of using such sources for phase contrast imaging of micro-calcifications included in a breast tissue. In our study we analyzed the phase and amplitude distribution of the TBS source and we showed that this source can be used for phase contrast imaging since the source coherence at the sample position is sufficiently high for achieving good contrast and micrometer spatial resolution. Indeed the spatial coherence of a TBS source is closer to that of a synchrotron radiation source, and much better than that of a laboratory source. Moreover, we showed the advantages of phase imaging with respect to standard absorption imaging, in the specific case of micro-calcifications detection.

  2. Design and development of single stage purification of papain using Ionic Liquid based aqueous two phase extraction system and its Partition coefficient studies

    Directory of Open Access Journals (Sweden)

    Senthilkumar Rathnasamy

    2013-04-01

    Full Text Available As an emerging trend in bioseparation, aqueous two phase extractions based on phosponium ionic liquid have been utilized in this work to extract papain from Carica papaya fruit latex and the same wascompared with conventional aqueous two phase extraction system. Factors affecting the partition coefficient of papain such as ionic liquid concentration, pH of the extraction system and temperature have been investigated. The optimization studies show that ionic liquid concentrations and pH are majorly influencing the phaseformations and papain partitioning. It reveals the importance of electrostatic and hydrophobic interactions in the papain partitioning. Purification studies performed on Gel Filtration Chromatography shows that 96% of the papain enzyme could be extracted with the phosponium based ionic liquid in a single stage extraction. The final fraction containing papain enzyme was confirmed by SDS Page analysis.

  3. Simultaneous separation/enrichment and detection of trace ciprofloxacin and lomefloxacin in food samples using thermosensitive smart polymers aqueous two-phase flotation system combined with HPLC.

    Science.gov (United States)

    Lu, Yang; Chen, Bo; Yu, Miao; Han, Juan; Wang, Yun; Tan, Zhenjiang; Yan, Yongsheng

    2016-11-01

    Smart polymer aqueous two phase flotation system (SPATPF) is a new separation and enrichment technology that integrated the advantages of the three technologies, i.e., aqueous two phase system, smart polymer and flotation sublation. Ethylene oxide and propylene oxide copolymer (EOPO)-(NH4)2SO4 SPATPF is a pretreatment technique, and it is coupled with high-performance liquid chromatography to analyze the trace ciprofloxacin and lomefloxacin in real food samples. The optimized conditions of experiment were determined in the multi-factor experiment by using response surface methodology. The flotation efficiency of lomefloxacin and ciprofloxacin was 94.50% and 98.23% under the optimized conditions. The recycling experimentsshowed that the smart polymer EOPO could use repeatedly, which will reduce the cost in the future application. PMID:27211613

  4. Source Separation and Clustering of Phase-Locked Subspaces: Derivations and Proofs

    OpenAIRE

    Almeida, Miguel; Schleimer, Jan-Hendrik; Bioucas-Dias, José; Vigário, Ricardo

    2011-01-01

    Due to space limitations, our submission "Source Separation and Clustering of Phase-Locked Subspaces", accepted for publication on the IEEE Transactions on Neural Networks in 2011, presented some results without proof. Those proofs are provided in this paper.

  5. Microcalorimetric Study on the Oscillating System of Two-phase Reaction of Aqueous Acid with Primary Amine in Chloroform

    Institute of Scientific and Technical Information of China (English)

    ZHANG,Hong-Lin; YU,Xiu-Fang; LU,Cheng-Xue; SUN,Si-Xiu; GUO,Guo-Hua; FU,Xun

    2003-01-01

    It has been found that the two-phase reactions of aqueous HCl,HOAc or H3PO4 with primary amine N1923 in chloroform are oscillating reactions. Their power-time curves were measured by the titration microcalorimetric method, and the induction period (tin).The first oscillating period (tp.1) and the second oscillating period(tp.2 ) were determined.The apparent activating parameters and the orders of the oscillating systems were calculated and the following relationships were established: for the oscillating system of hydrochloric acid tin∝c0.147HCIexp(1.35×103/T),.tp.1∝c0.241HCI·exp(4.33×103/T),tp.2∝c0.290HCIexp(5.59×103/T);for the oscillating system of acetic acid, tm∝c0.883HOAcexp(2.32×103/T),tp.1∝c0.399HOAc·exp(4.50×103/T),tp.2∝c0.301HOAcexp(5.88×103/T),for the oscillating system of phosphoric acid, tim∝c1.14H3PO4exp(7.70×104]T),tp.1∝c1.42H3PO4exp(1.14×104/T),tp.2∝c1.47H3PO4exp(1.27×104/T).

  6. Tea bag filter paper as a novel protective membrane for micro-solid phase extraction of butachlor in aqueous samples.

    Science.gov (United States)

    Pelden, Tshering; Thammaknet, Chongdee; Thavarungkul, Panote; Kanatharana, Proespichaya

    2014-01-01

    An innovative, cost-effective, simple, and environmental friendly tea bag filter paper protected micro-solid phase extraction (μ-SPE) technique was developed for the first time with the aim to miniaturize and minimize the use of organic solvents for the extraction and determination of butachlor in aqueous samples. The μ-SPE device was produced by packing 3.0 mg of an easily synthesized new sorbent, hydroxyl-functionalized polypyrrole (OH-PPY), inside a small tea bag filter paper sachet (1.0 cm × 0.5 cm) that served as a protective envelope. Both the extraction and desorption procedures were facilitated by sonication. Due to the high porosity and the fast water absorption of the tea bag filter paper, the analyte could easily diffuse through and enhance the interaction with the sorbent. Under the optimized conditions for the GC-ECD and the μ-SPE, the limit of detection (S/N ≥ 3) was 2.0 μg L(-1) while the limit of quantitation (S/N ≥ 10) was 10.0 μg L(-1). The recoveries of the butachlor spiked at 0.050, 0.10, and 0.50 μg mL(-1) ranged from 77.9 ± 3.0 to 112.5 ± 2.9%. The proposed method was successfully applied for the determination of butachlor in water samples from paddy cultivation sites. The levels found were from non-detectable to 24.71 ± 0.37 μg L(-1).

  7. Partitioning and purification of extracellular β-1,3-1,4-glucanase in aqueous two-phase systems

    Institute of Scientific and Technical Information of China (English)

    HE Guo-qing; ZHANG Xiu-yan; TANG Xing-jun; CHEN Qi-he; RUAN Hui

    2005-01-01

    The partition behaviors of β-1,3-1,4-glucanase, α-amylase and neutral proteases from clarified and whole fermentation broths of Bacillus subtilis ZJF-1A5 were investigated. An aqueous two-phase system (polyethylene glycol (PEG)/MgSO4)was examined with regard to the effects of PEG molecular weight (MW) and concentration, MgSO4 concentration, pH and NaCl concentration on enzyme partition and extraction. The MW and concentration of PEG were found to have significant effects on enzyme partition and extraction with low MW PEG showing the greatest benefit in the partition and extraction of β-glucanase with the PEG/MgSO4 system. MgSO4 concentration influenced the partition and extraction of β-glucanase significantly. pH had little effect on β-glucanase or proteases partition but affected α-amylase partition when pH was over 7.0. The addition of NaCl had little effect on the partition behavior of β-glucanase but had very significant effects on the partitioning of α-amylase and on the neutral proteases. The partition behaviors of β-glucanase, α-amylase and proteases in whole broth were also investigated and results were similar to those obtained with clarified fermentation broth. A two-step process for purifying β-glucanase was developed, which achieved β-glucanase recovery of 65.3% and specific activity of 14027 U/mg, 6.6 times improvement over the whole broth.

  8. Partition separation and characterization of the polyhydroxyalkanoates synthase produced from recombinant Escherichia coli using an aqueous two-phase system.

    Science.gov (United States)

    Lan, John Chi-Wei; Yeh, Chun-Yi; Wang, Chih-Chi; Yang, Yu-Hsuan; Wu, Ho-Shing

    2013-10-01

    Polyhydroxyalkanoates (PHAs) are renewable and biodegradable polyesters which can be synthesized either by numerous of microorganisms in vivo or synthase in vitro. The synthesis of PHAs in vitro requires an efficient separation for high yield of purified enzyme. The recombinant Escherichia coli harboring phaC gene derived from Ralstonia eutropha H16 was cultivated in the chemically defined medium for overexpression of synthase in the present work. The purification and characteristics of PHA synthase from clarified feedstock by using aqueous two-phase systems (ATPS) was investigated. The optimized concentration of ATPS for partitioning PHA synthase contained polyethylene glycol 6000 (30%, w/w) and potassium phosphate (8%, w/w) with 3.25 volume ratio in the absence of NaCl at pH 8.7 and 4°C. The results showed that the partition coefficient of enzyme activity and protein content are 6.07 and 0.22, respectively. The specific activity, selectivity, purification fold and recovery of phaC(Re) achieved 1.76 U mg⁻¹, 29.05, 16.23 and 95.32%, respectively. Several metal ions demonstrated a significant effect on activity of purified enzyme. The purified enzyme displayed maximum relative activity as operating condition at pH value of 7.5 and 37°C. As compared to conventional purification processes, ATPS can be a promising technique applied for rapid recovery of PHA synthase and preparation of large quantity of PHA synthase on synthesis of P(3HB) in vitro.

  9. Formation of residual non-aqueous phase liquid in a water-wet system: Investigation by bulk electrical conductivity

    Science.gov (United States)

    Dudley, L. M.; Das, N.

    2011-12-01

    Managing contaminated sites can be expensive, but multi-phase models can be an effective tool to predict the subsurface behavior of contaminants and help reduce associated costs. One of the major deficiencies of such models is the prediction of the amount of residual non-aqueous phase liquids (NAPL). In order to accurately predict the behavior of residual NAPL, it is important to understand the formation of residual NAPL. The presence of residual NAPL in the vadose zone has been demonstrated by many researchers, but the conditions under which residual NAPL is formed are poorly understood. Traditionally permeability-saturation pressure (k-s-p) relations have been used to demonstrate the formation of residual NAPL. We used electrical conductivity to investigate the process of formation of residual NAPL. Experiments were conducted in a teflon jar (diameter=106.9mm and height= 64.8mm) packed as uniformly as possible with a washed, oven-dried soil sample. The soil was washed with distilled, deionized water to reduce any dissolved salt, so that the soil salinity was consistent. A Wenner array was adapted to a round cell with four neighboring stainless steel electrodes were installed into the cell wall with equal spacing. The cell has two porous cups connected; one is saturated with water and another with Oleic acid. Soil resistance measurements were made with a model 1625 Fluke Earth/Ground Tester. The system was initially water wet, drained to the irreducible water content and then NAPL was introduced to the system using peristaltic pump until the desired NAPL saturation was reached. Once equilibrium was reached, NAPL was drained 5-10 ml at a time and the pressure head was measured. Once the NAPL reached irreducible level, i.e. no NAPL would come out of the system when drainage was unrestricted; water was again imbibed into the system. For each step of fluid imbibition and drainage resistivity values were recorded. During the first few increments of oil imbibition

  10. Quantum chemical analysis of the energy of proton transfer from phenol and chlorophenols to H2O in the gas phase and in aqueous solution

    Science.gov (United States)

    Schüürmann, Gerrit

    1998-12-01

    Proton transfer energies of phenol and 14 chlorophenols with H2O as a base are analyzed in the gas phase and in solution using quantum chemical methods at the semiempirical and ab initio level of computation. The effect of aqueous solution was accounted for by applying the density functional theory (DFT) implementation of the conductor-like screening model (COSMO) as well as semiempirical continuum-solvation models. The results reveal substantial and systematic overestimations of the free energies of proton transfer as derived from experimental solution-phase pKa data. This can be traced back to both deficiencies in the current model parameterization as well as to limitations of the underlying gas-phase quantum chemical models, which is further illustrated by additional complete-basis-set (CBS) calculations for the proton transfer reaction with phenol. In contrast, the relative pKa trend is reflected well by COSMO-DFT calculations with correlation coefficients (adjusted for degrees of freedom) of 0.96. Decomposition of the dissociation energy in aqueous solution into a gas-phase term and a term summarizing the solvation contributions provides new insights into the effect of solvation on proton transfer energies, and yields mechanistic explanations for the observed differences in the gas-phase and solution-phase acidity orders of various subgroups of the compounds.

  11. Reversible hydration and aqueous exfoliation of the acetate-intercalated layered double hydroxide of Ni and Al: Observation of an ordered interstratified phase

    Energy Technology Data Exchange (ETDEWEB)

    Manohara, G.V. [Department of Chemistry, The Central College Campus, Bangalore University, Bangalore 560 001 (India); Vishnu Kamath, P., E-mail: vishnukamath8@hotmail.com [Department of Chemistry, The Central College Campus, Bangalore University, Bangalore 560 001 (India); Milius, Wolfgang [Department of Inorganic Chemistry I, University of Bayreuth, Bayreuth D-95440 (Germany)

    2012-12-15

    Acetate-intercalated layered double hydroxides (LDHs) of Ni and Al undergo reversible hydration in the solid state in response to the ambient humidity. The LDH with a high layer charge (0.33/formula unit) undergoes facile hydration in a single step, whereas the LDH with a lower layer charge (0.24/formula unit) exhibits an ordered interstratified intermediate, comprising the hydrated and dehydrated layers stacked alternatively. This phase, also known as the staged S-2 phase, coexists with the end members suggesting the existence of a solution-type equilibrium between the S-2 phase and the end members of the hydration cycle. These LDHs also undergo facile aqueous exfoliation into 2-5 nm-thick tactoids with a radial dimension of 0.2-0.5 {mu}m. - Graphical abstract: Schematic of the hydrated, dehydrated and interstratified phases observed during the hydration-dehydration of Ni/Al-CH{sub 3}COO LDH. Highlights: Black-Right-Pointing-Pointer Ni/Al-acetate LDHs were synthesized by HPFS method by hydrolysis of acetamide. Black-Right-Pointing-Pointer Intercalated acetate ion shows reversible hydration with variation in humidity. Black-Right-Pointing-Pointer An ordered interstratified phase was observed during hydration/dehydration cycle. Black-Right-Pointing-Pointer A solution type equilibrium is observed between hydration-dehydration phases. Black-Right-Pointing-Pointer These LDHs undergo facile aqueous exfoliation.

  12. Phase recovery in NMF for audio source separation: an insightful benchmark

    OpenAIRE

    Magron, Paul; Badeau, Roland; David, Bertrand

    2016-01-01

    Nonnegative Matrix Factorization (NMF) is a powerful tool for decomposing mixtures of audio signals in the Time-Frequency (TF) domain. In applications such as source separation, the phase recovery for each extracted component is a major issue since it often leads to audible artifacts. In this paper, we present a methodology for evaluating various NMF-based source separation techniques involving phase reconstruction. For each model considered, a comparison between two approaches (blind separat...

  13. In-line phase contrast for weakly absorbing materials with a microfocus x-ray source

    Institute of Scientific and Technical Information of China (English)

    Zhang Di; Li Zheng; Huang Zhi-Feng; Yu Ai-Min; Sha Wei

    2006-01-01

    For weakly absorbing materials, image contrast can be enhanced by phase contrast in formation. The effectiveness of the in-line phase contrast technique relies on its ability to record intensity data which contain information on the x-ray's phase shift. Four kinds of approaches to the relationship between intensity distribution and phase shift are reviewed and discussed. A micro-focal x-ray source with high geometrical magnification is used to acquire phase contrast images. A great improvement on image quality is shown and geometrical parameters are modified for comparison between different imaging positions.

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

    Science.gov (United States)

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

    2015-10-14

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

  15. Phase equilibrium measurements for semi-clathrate hydrates of the (CO2 + N2 + tetra-n-butylammonium bromide) aqueous solution system

    International Nuclear Information System (INIS)

    Highlights: ► Semi-clathrate hydrate phase equilibrium for CO2+N2+TBAB aqueous solutions. ► Measurements for temperatures from 277.1 K to 293.2 K and pressures up to 16.21 MPa. ► TBAB has a promotion effect on semi-clathrate hydrate formation. - Abstract: The application of semi-clathrate hydrate formation technology for gas separation purposes has gained much attention in recent years. Consequently, there is a demand for experimental data for relevant semi-clathrate hydrate phase equilibria. In this work, semi-clathrate hydrate dissociation conditions for the system comprising mixtures of {CO2 (0.151/0.399 mole fraction) + N2 (0.849/0.601 mole fraction) + 0.05, 0.15, and 0.30 mass fraction tetra-n-butylammonium bromide (TBAB)} aqueous solutions have been measured and are reported. An experimental apparatus which was designed and built in-house was used for the measurements using the isochoric pressure-search method. The range of conditions for the measurements was from 277.1 K to 293.2 K for temperature and pressures up to 16.21 MPa. The phase equilibrium data measured demonstrate the high hydrate promotion effects of TBAB aqueous solutions.

  16. 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

  17. Purification of a fibrinolytic protease from Mucor subtilissimus UCP 1262 by aqueous two-phase systems (PEG/sulfate).

    Science.gov (United States)

    Nascimento, Thiago Pajeú; Sales, Amanda Emmanuelle; Porto, Camila Souza; Brandão, Romero Marcos Pedrosa; de Campos-Takaki, Galba Maria; Teixeira, José Antônio Couto; Porto, Tatiana Souza; Porto, Ana Lúcia Figueiredo; Converti, Attilio

    2016-07-01

    A fibrinolytic protease from M. subtilissimus UCP 1262 was recovered and partially purified by polyethylene glycol (PEG)/sodium sulfate aqueous two-phase systems (ATPS). The simultaneous influence of PEG molar mass, PEG concentration and sulfate concentration on the enzyme recovery was first investigated using a 2(3) full factorial design, and the Response Surface Methodology used to identify the optimum conditions for enzyme extraction by ATPS. Once the best PEG molar mass for the process had been selected (6000g/mol), a two-factor central composite rotary design was applied to better evaluate the effects of the other two independent variables. The fibrinolytic enzyme was shown to preferentially partition to the bottom phase with a partition coefficient (K) ranging from 0.2 to 0.7. The best results in terms of enzyme purification were obtained with the system formed by 30.0% (w/w) PEG 6000g/mol and 13.2% (w/w) sodium sulfate, which ensured a purification factor of 10.0, K of 0.2 and activity yield of 102.0%. SDS-PAGE and fibrin zymography showed that the purified protease has a molecular mass of 97kDa and an apparent isoelectric point of 5.4. When submitted to assays with different substrates and inhibitors, it showed selectivity for succinyl-l-ala-ala-pro-l-phenylalanine-p-nitroanilide and was almost completely inhibited by phenylmethylsulfonyl fluoride, behaving as a chymotrypsin-like protease. At the optimum temperature of 37°C, the enzyme residual activity was 94 and 68% of the initial one after 120 and 150min of incubation, respectively. This study demonstrated that M. subtilissimus protease has potent fibrinolytic activity compared with similar enzymes produced by solid-state fermentation, therefore it may be used as an agent for the prevention and therapy of thrombosis. Furthermore, it appears to have the advantages of low cost production and simple purification. PMID:27183214

  18. Ordered mesoporous carbon film as an effective solid-phase microextraction coating for determination of benzene series from aqueous media

    International Nuclear Information System (INIS)

    The present work reports preparation of ordered mesoporous carbon (OMC) film supported on a graphite fiber as a new type of solid-phase microextraction (SPME) fiber for determination of benzene series from aqueous media. The strategy for the supported OMC film preparation was combined dip-coating technology with solvent evaporation-induced self-assembly (EISA) approach. A graphite fiber was immersed in an ethanol solution containing phenolic resin and Pluronic triblock copolymer. Upon solvent evaporation and subsequent pyrolysis under 700 °C, the phenolic resin and the surfactant self-assembled on the surface of the graphite fiber to form smooth OMC film. X-ray diffraction (XRD), transmission electron microscopy (TEM) and nitrogen isothermal adsorption results indicate that the resultant OMC film possesses well-ordered two dimensional hexagonal mesostructure with pore diameters of 4.5 nm and BET surfaces of 630 m2/g. Scanning electron microscopy (SEM) studies show the supported OMC film with thickness at 8.5 μm is continuous and defect-free. The SPME efficiency of the OMC fiber was evaluated by analysis of five benzene series (benzene, toluene, ethylbenzene, p-xylene and m-xylene) from water samples by gas chromatography-flame ionization detection (GC-FID). The analysis results indicate that the prepared OMC fiber has wide linear ranges (0.5–500 μg/L), low detection limits (0.01–0.05 μg/L) and good repeatabilities (4.0–5.8% for one fiber, 2.9–8.7% for fiber-to-fiber). Compared with commercial counterparts, the OMC fiber exhibits improved extraction efficiency for benzene series and PAHs. - Highlights: • Ordered mesoporous carbon film supported on graphite fiber was first reported as solid-phase microextraction coating. • The strategy for the film preparation was combined dip-coating technology with evaporation-induced self-assembly approach. • The obtained fiber showed enhanced thermal stability and organic solvents resistance. • The fiber

  19. Ordered mesoporous carbon film as an effective solid-phase microextraction coating for determination of benzene series from aqueous media

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Hui [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental Science and Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China); School of Geography Science, Nantong University, Nantong 226001 (China); Li, Jiansheng, E-mail: lijsh@mail.njust.edu.cn [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental Science and Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China); Jiang, Mingyue; Lu, Rui; Shen, Jinyou; Sun, Xiuyun; Han, Weiqing [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental Science and Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China); Wang, Lianjun, E-mail: wanglj@mail.njust.edu.cn [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental Science and Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China)

    2015-08-12

    The present work reports preparation of ordered mesoporous carbon (OMC) film supported on a graphite fiber as a new type of solid-phase microextraction (SPME) fiber for determination of benzene series from aqueous media. The strategy for the supported OMC film preparation was combined dip-coating technology with solvent evaporation-induced self-assembly (EISA) approach. A graphite fiber was immersed in an ethanol solution containing phenolic resin and Pluronic triblock copolymer. Upon solvent evaporation and subsequent pyrolysis under 700 °C, the phenolic resin and the surfactant self-assembled on the surface of the graphite fiber to form smooth OMC film. X-ray diffraction (XRD), transmission electron microscopy (TEM) and nitrogen isothermal adsorption results indicate that the resultant OMC film possesses well-ordered two dimensional hexagonal mesostructure with pore diameters of 4.5 nm and BET surfaces of 630 m{sup 2}/g. Scanning electron microscopy (SEM) studies show the supported OMC film with thickness at 8.5 μm is continuous and defect-free. The SPME efficiency of the OMC fiber was evaluated by analysis of five benzene series (benzene, toluene, ethylbenzene, p-xylene and m-xylene) from water samples by gas chromatography-flame ionization detection (GC-FID). The analysis results indicate that the prepared OMC fiber has wide linear ranges (0.5–500 μg/L), low detection limits (0.01–0.05 μg/L) and good repeatabilities (4.0–5.8% for one fiber, 2.9–8.7% for fiber-to-fiber). Compared with commercial counterparts, the OMC fiber exhibits improved extraction efficiency for benzene series and PAHs. - Highlights: • Ordered mesoporous carbon film supported on graphite fiber was first reported as solid-phase microextraction coating. • The strategy for the film preparation was combined dip-coating technology with evaporation-induced self-assembly approach. • The obtained fiber showed enhanced thermal stability and organic solvents resistance. • The

  20. Phase-sensitive optical coherence tomography-based vibrometry using a highly phase-stable akinetic swept laser source

    Science.gov (United States)

    Applegate, Brian E.; Park, Jesung; Carbajal, Esteban; Oghalai, John S.

    2015-12-01

    Phase-sensitive Optical Coherence Tomography (PhOCT) is an emerging tool for in vivo investigation of the vibratory function of the intact middle and inner ear. PhOCT is able to resolve micron scale tissue morphology in three dimensions as well as measure picometer scale motion at each spatial position. Most PhOCT systems to date have relied upon the phase stability offered by spectrometer detection. On the other hand swept laser source based PhOCT offers a number of advantages including balanced detection, long imaging depths, and high imaging speeds. Unfortunately the inherent phase instability of traditional swept laser sources has necessitated complex user developed hardware/software solutions to restore phase sensitivity. Here we present recent results using a prototype swept laser that overcomes these issues. The akinetic swept laser is electronically tuned and precisely controls sweeps without any mechanical movement, which results in high phase stability. We have developed an optical fiber based PhOCT system around the akinetic laser source that had a 1550 nm center wavelength and a sweep rate of 140 kHz. The stability of the system was measured to be 4.4 pm with a calibrated reflector, thus demonstrating near shot noise limited performance. Using this PhOCT system, we have acquired structural and vibratory measurements of the middle ear in a mouse model, post mortem. The quality of the results suggest that the akinetic laser source is a superior laser source for PhOCT with many advantages that greatly reduces the required complexity of the imaging system.

  1. Phase-sensitive optical coherence tomography-based vibrometry using a highly phase-stable akinetic swept laser source

    Energy Technology Data Exchange (ETDEWEB)

    Applegate, Brian E.; Park, Jesung; Carbajal, Esteban [Department of Biomedical Engineering, Texas A& M University, College Station, Texas (United States); Oghalai, John S. [Department of Otolaryngology - Head and Neck Surgery, Stanford University, Stanford, California (United States)

    2015-12-31

    Phase-sensitive Optical Coherence Tomography (PhOCT) is an emerging tool for in vivo investigation of the vibratory function of the intact middle and inner ear. PhOCT is able to resolve micron scale tissue morphology in three dimensions as well as measure picometer scale motion at each spatial position. Most PhOCT systems to date have relied upon the phase stability offered by spectrometer detection. On the other hand swept laser source based PhOCT offers a number of advantages including balanced detection, long imaging depths, and high imaging speeds. Unfortunately the inherent phase instability of traditional swept laser sources has necessitated complex user developed hardware/software solutions to restore phase sensitivity. Here we present recent results using a prototype swept laser that overcomes these issues. The akinetic swept laser is electronically tuned and precisely controls sweeps without any mechanical movement, which results in high phase stability. We have developed an optical fiber based PhOCT system around the akinetic laser source that had a 1550 nm center wavelength and a sweep rate of 140 kHz. The stability of the system was measured to be 4.4 pm with a calibrated reflector, thus demonstrating near shot noise limited performance. Using this PhOCT system, we have acquired structural and vibratory measurements of the middle ear in a mouse model, post mortem. The quality of the results suggest that the akinetic laser source is a superior laser source for PhOCT with many advantages that greatly reduces the required complexity of the imaging system.

  2. Phase-sensitive optical coherence tomography-based vibrometry using a highly phase-stable akinetic swept laser source

    International Nuclear Information System (INIS)

    Phase-sensitive Optical Coherence Tomography (PhOCT) is an emerging tool for in vivo investigation of the vibratory function of the intact middle and inner ear. PhOCT is able to resolve micron scale tissue morphology in three dimensions as well as measure picometer scale motion at each spatial position. Most PhOCT systems to date have relied upon the phase stability offered by spectrometer detection. On the other hand swept laser source based PhOCT offers a number of advantages including balanced detection, long imaging depths, and high imaging speeds. Unfortunately the inherent phase instability of traditional swept laser sources has necessitated complex user developed hardware/software solutions to restore phase sensitivity. Here we present recent results using a prototype swept laser that overcomes these issues. The akinetic swept laser is electronically tuned and precisely controls sweeps without any mechanical movement, which results in high phase stability. We have developed an optical fiber based PhOCT system around the akinetic laser source that had a 1550 nm center wavelength and a sweep rate of 140 kHz. The stability of the system was measured to be 4.4 pm with a calibrated reflector, thus demonstrating near shot noise limited performance. Using this PhOCT system, we have acquired structural and vibratory measurements of the middle ear in a mouse model, post mortem. The quality of the results suggest that the akinetic laser source is a superior laser source for PhOCT with many advantages that greatly reduces the required complexity of the imaging system

  3. Liquid-liquid equilibrium and partitioning features of bovine trypsin in Ucon 50 HB5100 /sodium citrate aqueous two phase systems

    OpenAIRE

    Tubío, Gisela; Venâncio, Armando; J. A. Teixeira; Nerli, Bibiana B.; Picó, Guillermo A.

    2008-01-01

    The phase diagrams of Ucon 50-HB-5100, a non-ionic random copolymer of ethylene oxide and propylene oxide (EOPO) and sodium citrate aqueous two-phase systems were determined at different pHs (5.20 and 8.20) and temperatures (5, 20 and 40º C). The binodal curves were determined by refractive index and enzymatic assay of the solution and described using a four-parameter sigmoidal equation, the reliability of the measured tie line compositions was ascertained by correlation equations...

  4. A Database of Phase Calibration Sources and their Radio Spectra for the Giant Metrewave Radio Telescope

    CERN Document Server

    Lal, Dharam V; Sherkar, Sachin S

    2016-01-01

    We are pursuing a project to build a database of phase calibration sources suitable for Giant Metrewave Radio Telescope (GMRT). Here we present the first release of 45 low frequency calibration sources at 235 MHz and 610 MHz. These calibration sources are broadly divided into quasars, radio galaxies and unidentified sources. We provide their flux densities, models for calibration sources, (u,v) plots, final deconvolved restored maps and clean-component lists/files for use in the Astronomical Image Processing System (AIPS) and the Common Astronomy Software Applications (CASA). We also assign a quality factor to each of the calibration sources. These data products are made available online through the GMRT observatory website. In addition we find that (i) these 45 low frequency calibration sources are uniformly distributed in the sky and future efforts to increase the size of the database should populate the sky further, (ii) spectra of these calibration sources are about equally divided between straight, curve...

  5. Optical phase-locked loop signal sources for phased-array communications antennas

    Science.gov (United States)

    Langley, Lloyd N.; Edge, Colin; Wale, Michael J.; Gliese, Ulrik B.; Seeds, Alwyn J.; Walton, Channing; Wright, James G.; Coryell, Louis A.

    1997-10-01

    A coherent, optical heterodyne approach to signal generation and beamforming is particularly advantageous in multi-beam mobile phased arrays. Use of optical technology allows an optimum distribution of weight and power to be achieved between the antenna face and central electronics, together with an efficient implementation of the beamforming function and a modular design approach in which the basic building blocks are frequency-independent. Systems of this type employ a pair of optical carriers with a difference frequency equal to the required microwave signal. Phased- locking is necessary in order to achieve sufficiently low phase noise in the radio communication link. Optical phase locked loops (OPLLs) have been shown to be potential candidates for this application, yet work still needs to be done to bring them from the laboratory to field demonstrations. This paper describes the construction of a laser-diode OPLL subsystem for evaluation in a proof-of- concept beamforming system. This involves optimization of the loop design, development of single-frequency laser diodes with the correct linewidth, modulation and tuning characteristics and integration into a micro-optic assembly with custom wideband electronics.

  6. Study on the Intermediate in the o-Phenylenediamine Oxidative Reaction Using Hemoglobin as A Mimetic Peroxidase in Aqueous-Organic Two Phase

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Hemoglobin was used as a mimetic enzyme for peroxidase to catalyze the oxidative reaction ofo-phenylenediamine with H2O2 which functioned as an oxidant. The relationship between physicochemicalproperties of the intermediate and enzymatic activity of hemoglobin was studied. Since the solubility of theintermediate in the reaction is higher in butanol phase than in water phase, the intermediate itself diffusedfrom the aqueous phase to the butanol phase. The experimental results showed that the rate of product andthe stability of intermediate were associated with the temperature and the pH value of the buffer. The for-mation rate of intermediate and half-life period reveal the maximal in pH7, nevertheless, the whole rate ofthe catalytic reaction is the greatest in pH5, which the ratio of the initial rate in final product formationcompared to that intermediate formation is the greatest.

  7. Source reconciliation of atmospheric gas-phase and particle-phase pollutants during a severe photochemical smog episode.

    Science.gov (United States)

    Schauer, James J; Fraser, Matthew P; Cass, Glen R; Simoneit, Bernd R T

    2002-09-01

    A comprehensive organic compound-based receptor model is developed that can simultaneously apportion the source contributions to atmospheric gas-phase organic compounds, semivolatile organic compounds, fine particle organic compounds, and fine particle mass. The model is applied to ambient data collected at four sites in the south coast region of California during a severe summertime photochemical smog episode, where the model determines the direct primary contributions to atmospheric pollutants from 11 distinct air pollution source types. The 11 sources included in the model are gasoline-powered motor vehicle exhaust, diesel engine exhaust, whole gasoline vapors, gasoline headspace vapors, organic solvent vapors, whole diesel fuel, paved road dust, tire wear debris, meat cooking exhaust, natural gas leakage, and vegetative detritus. Gasoline engine exhaust plus whole gasoline vapors are the predominant sources of volatile organic gases, while gasoline and diesel engine exhaust plus diesel fuel vapors dominate the emissions of semivolatile organic compounds from these sources during the episode studied at all four air monitoring sites. The atmospheric fine particle organic compound mass was composed of noticeable contributions from gasoline-powered motor vehicle exhaust, diesel engine exhaust, meat cooking, and paved road dust with smaller but quantifiable contributions from vegetative detritus and tire wear debris. In addition, secondary organic aerosol, which is formed from the low-vapor pressure products of gas-phase chemical reactions, is found to be a major source of fine particle organic compound mass under the severe photochemical smog conditions studied here. The concentrations of secondary organic aerosol calculated in the present study are compared with previous fine particle source apportionment results for less intense photochemical smog conditions. It is shown that estimated secondary organic aerosol concentrations correlate fairly well with the

  8. Chitosan-Coated Magnetic Nanoparticles Prepared in One-Step by Precipitation in a High-Aqueous Phase Content Reverse Microemulsion

    Directory of Open Access Journals (Sweden)

    María Guadalupe Pineda

    2014-07-01

    Full Text Available Chitosan-coated magnetic nanoparticles (CMNP were prepared in one-step by precipitation in a high-aqueous phase content reverse microemulsion in the presence of chitosan. The high-aqueous phase concentration led to productivities close to 0.49 g CMNP/100 g microemulsion; much higher than those characteristic of precipitation in reverse microemulsions for preparing magnetic nanoparticles. The obtained nanoparticles present a narrow particle size distribution with an average diameter of 4.5 nm; appearing to be formed of a single crystallite; furthermore they present superparamagnetism and high magnetization values; close to 49 emu/g. Characterization of CMNP suggests that chitosan is present as a non-homogeneous very thin layer; which explains the slight reduction in the magnetization value of CMNP in comparison with that of uncoated magnetic nanoparticles. The prepared nanoparticles show high heavy ion removal capability; as demonstrated by their use in the treatment of Pb2+ aqueous solutions; from which lead ions were completely removed within 10 min.

  9. X-ray Amorphous Phases in Antarctica Dry Valley Soils: Insight into Aqueous Alteration Processes on Mars?

    Science.gov (United States)

    Ming, D. W.; Morris, R. V.; Rampe, E. B.; Quinn, J. E.; Graff, T. G.

    2015-12-01

    The Chemistry and Mineralogy (CheMin) instrument onboard the Mars Curiosity rover has detected abundant amounts (approx. 25-30 wt. %) of X-ray amorphous materials in a windblown deposit (Rocknest) and in a sedimentary mudstone (Cumberland and John Klein) in Gale crater. On Earth, X-ray amorphous components are common in soils and sediments, but usually not as abundant as detected in Gale crater. One hypothesis for the abundant X-ray amorphous materials on Mars is limited interaction of liquid water with surface materials, kinetically inhibiting maturation to more crystalline phases. The objective of this study was to characterize the chemistry and mineralogy of soils formed in the Antarctica Dry Valleys, one of the driest locations on Earth. Two soils were characterized from different elevations, including a low elevation, coastal, subxerous soil in Taylor Valley and a high elevation, ultraxerous soil in University Valley. A variety of techniques were used to characterize materials from each soil horizon, including Rietveld analysis of X-ray diffraction data. For Taylor Valley soil, the X-ray amorphous component ranged from about 4 wt. % in the upper horizon to as high as 15 wt. % in the lowest horizon just above the permafrost layer. Transmission electron microscopy indicated that the presence of short-range ordered (SRO) smectite was the most likely candidate for the X-ray amorphous materials in the Taylor Valley soils. The SRO smectite is likely an aqueous alteration product of mica inherited from granitic materials during glaciation of Taylor Valley. The drier University Valley soil had lower X-ray amorphous contents of about 5 wt. % througout the profile. The X-ray amorphous materials in University Valley are attributed to nanoparticles of TiO2 and possibly amorphous SiO2. The high abundance of X-ray amorphous materials in Taylor Valley is surprising for one of the driest places on Earth. These materials may have been physically and chemical altered during

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

    Science.gov (United States)

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

    2016-04-01

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

  11. Aqueous and solid phase speciation of arsenic in a Bengali aquifer using IC-ICP-MS and EXAFS

    Science.gov (United States)

    Gault, A. G.; Davidson, L. E.; Lythgoe, P. R.; Charnock, J. M.; Chatterjee, D.; Abou-Shakra, F. R.; Walker, H. J.; Polya, D. A.

    2003-04-01

    Contamination of groundwater and drinking water supplies with arsenic has been reported in many parts of the world and constitutes a serious public health threat. Nowhere is this more apparent than in West Bengal and Bangladesh where arsenic concentrations exceed both World Health Organisation (WHO) and national limits in drinking water supplies leading to what has been described as the worst mass poisoning of a human population in history. Knowledge of both aqueous and solid phase speciation of arsenic in such hazardous arsenic-rich groundwaters is crucial to understanding the processes controlling arsenic release. We report here preliminary work involving the determination of dissolved arsenic speciation in West Bengali groundwaters and extended X-ray absorption fine structure (EXAFS) analysis of the associated sediment. Groundwater samples collected from Nadia district, West Bengal were analysed for arsenic speciation by ion chromatography-inductively coupled plasma-mass spectrometry (IC-ICP-MS) within 14 days of collection. Total arsenic concentrations exceeding 850 ug/L were determined; inorganic arsenic constituted the bulk of the dissolved arsenic burden with As(III) as the dominant form. Minor amounts of methylated arsenicals were also detected, however, their concentration did not exceed 5 ug/L. The local coordination environment of arsenic in sediment associated with such groundwaters was probed using K-edge As EXAFS. This revealed that arsenic exists predominantly in its oxidised form, As(V), most likely adsorbed as bidentate arsenate tetrahedra on metal (Fe and/or Al) oxide/hydroxide surfaces, although incorporation of arsenic into a metal oxide structure cannot be unequivocally ruled out. Arsenic was found to occur in several different coordination environments and this, together with the low concentration (arsenic in the sediment, prevented the unambiguous assignment of the second coordination sphere. The analysis of the trends of key groundwater

  12. 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

  13. INTERACTION OF AQUEOUS SOLUTIONS OF CHLORINE WITH MALIC ACID, TARTARIC ACID, AND VARIOUS FRUIT JUICES, A SOURCE OF MUTAGENS

    Science.gov (United States)

    The interactions of aqueous solutions of chlorine with some fruit acids (citric acid, DL-malic acid, and L-tartaric acid) at different pH values were studied. iethyl ether extraction followed by GC/MS analysis indicated that a number of mutagens (certain chlorinated propanones an...

  14. 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.

  15. Reconstruction of Sound Source Pressures in an Enclosure Using the Phased Beam Tracing Method

    DEFF Research Database (Denmark)

    Jeong, Cheol-Ho; Ih, Jeong-Guon

    2009-01-01

    Source identification in an enclosure is not an easy task due to complicated wave interference and wall reflections, in particular, at mid-high frequencies. In this study, a phased beam tracing method was applied to the reconstruction of source pressures inside an enclosure at medium frequencies....... First, surfaces of an extended source are divided into reasonably small segments. From each source segment, one beam is projected into the field and all emitted beams are traced. Radiated beams from the source reach array sensors after traveling various paths including the wall reflections. Collecting...... all the pressure histories at the field points, source-observer relations can be constructed in a matrix-vector form for each frequency. By multiplying the measured field data with the pseudo-inverse of the calculated transfer function, one obtains the distribution of source pressure. An omni...

  16. Batch, Kinetic and Equilibrium Studies of Chromium (Vi From Aqueous Phase Using Activated Carbon Derived From Lantana Camara Fruit

    Directory of Open Access Journals (Sweden)

    K. Nithya

    2015-12-01

    Full Text Available Batch experiments have been conducted to determine the maximum adsorption capacity of activated carbon derived from Lantana camara fruit to remove hexavalent chromium from aqueous solution. The removal efficiency and uptake capacity of the biosorbent were determined by varying several batch level parameters. Highest removal efficiency of the biosorbent was found to be almost 99% under optimal conditions. Maximum monolayer adsorption capacity was determined to be 86 mg/g. The experimental data best fitted with Langmuir adsorption isotherm and pseudo second order model. These findings conclude that the selected biosorbent has more promising features in binding hexavalent chromium in aqueous media.

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

    Institute of Scientific and Technical Information of China (English)

    ZHANG Junwei; WANG Yan; PENG Qijun

    2013-01-01

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

  18. Chemical insights, explicit chemistry, and yields of secondary organic aerosol from OH radical oxidation of methylglyoxal and glyoxal in the aqueous phase

    Directory of Open Access Journals (Sweden)

    Y. B. Lim

    2013-09-01

    Full Text Available Atmospherically abundant, volatile water-soluble organic compounds formed through gas-phase chemistry (e.g., glyoxal (C2, methylglyoxal (C3, and acetic acid have great potential to form secondary organic aerosol (SOA via aqueous chemistry in clouds, fogs, and wet aerosols. This paper (1 provides chemical insights into aqueous-phase OH-radical-initiated reactions leading to SOA formation from methylglyoxal and (2 uses this and a previously published glyoxal mechanism (Lim et al., 2010 to provide SOA yields for use in chemical transport models. Detailed reaction mechanisms including peroxy radical chemistry and a full kinetic model for aqueous photochemistry of acetic acid and methylglyoxal are developed and validated by comparing simulations with the experimental results from previous studies (Tan et al., 2010, 2012. This new methylglyoxal model is then combined with the previous glyoxal model (Lim et al., 2010, and is used to simulate the profiles of products and to estimate SOA yields. At cloud-relevant concentrations (~ 10−6 − ~ 10−3 M; Munger et al., 1995 of glyoxal and methylglyoxal, the major photooxidation products are oxalic acid and pyruvic acid, and simulated SOA yields (by mass are ~ 120% for glyoxal and ~ 80% for methylglyoxal. During droplet evaporation oligomerization of unreacted methylglyoxal/glyoxal that did not undergo aqueous photooxidation could enhance yields. In wet aerosols, where total dissolved organics are present at much higher concentrations (~ 10 M, the major oxidation products are oligomers formed via organic radical–radical reactions, and simulated SOA yields (by mass are ~ 90% for both glyoxal and methylglyoxal. Non-radical reactions (e.g., with ammonium could enhance yields.

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

    Science.gov (United States)

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

    2016-01-01

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

  20. Cobalt-60 heat source demonstration program. Phase III. Fabrication. Final report

    Energy Technology Data Exchange (ETDEWEB)

    1973-06-01

    Significant accomplishments completed during Phase III of the /sup 60/Co Heat Source Demonstration program include the following: encapsulation of 2 MCi of /sup 60/Co; fabrication of the heat source, including the ASME coded pressure vessel/core assembly, and biological shielding; endurance testing of a prototype heat pipe for a period of 28 months; fabrication and qualification of the heat pipe emergency cooling subsystem; issue of the safety evaluation report, reference 3, and the operations manual, reference 4; and heat source assembly. The planned demonstration test program was modified to include testing of a total power system. Based on an evaluation of available power conversion systems, which included the closed-cycle Brayton and organic Rankine systems, the closed-cycle Brayton system was selected for use. Selection was based on advantages offered by the direct coupling of this conversion system with the gas-cooled heat source. In implementing the test program, the AiResearch BCD power conversion system was to be coupled to the heat source following initial heat source performance testing and part way through the endurance test. In accordance with the program redirection the following Phase IV checkout operations were completed to evaluate procedural and hardware acceptability: heat source dummy fueling; fueling cask sielding survey; and heat source shielding survey (single pin). Completion of these latter activities verified the acceptability of critical characteristics of the heat source and its supporting equipment.

  1. An efficient method for synthesis of phenacyl derivatives under homogeneous phase transfer catalyst condition in aqueous media

    Institute of Scientific and Technical Information of China (English)

    Soheil Sayyahi; Jafar Saghanezhad

    2011-01-01

    In this letter, a mild and efficient procedure for synthesis of phenacyl derivatives under homogenous catalysis in the presence of tetrabutylammonium bromide in aqueous media is described. The nucleophilic substitution reactions were performed under ecofriendly conditions and gave the corresponding products in high yields and short reaction times.

  2. Novel, Four-Switch, Z-Source Three-Phase Inverter

    DEFF Research Database (Denmark)

    Antal, Robert; Muntean, Nicolae; Boldea, Ion;

    2010-01-01

    This paper presents a new z-source three phase inverter topology. The proposed topology combines the advantages of a traditional four-switch three-phase inverter with the advantages of the z impedance network (one front-end diode, two inductors and two X connected capacitors). This new topology......, besides the self-boost property, has low switch count and it can operate as a buck-boost inverter. In contrast to standard four-switch three-phase inverter which operates at half dc input voltage the proposed four-switch z-source inverter, by self boosting, brings the output voltage at same (or higher......) value as in six switch standard three-phase inverter. The article presents the derivation of the equations describing the operation of the converter based on space vector analysis, validation through digital simulations in PSIM and preliminary experimental results on a laboratory setup with a dsPIC30F...

  3. Calculation of liquid-liquid equilibrium of aqueous two-phase systems using a chemical-theory-based excess Gibbs energy model

    Directory of Open Access Journals (Sweden)

    Pessôa Filho P. A.

    2004-01-01

    Full Text Available Mixtures containing compounds that undergo hydrogen bonding show large deviations from ideal behavior. These deviations can be accounted for through chemical theory, according to which the formation of a hydrogen bond can be treated as a chemical reaction. This chemical equilibrium needs to be taken into account when applying stability criteria and carrying out phase equilibrium calculations. In this work, we illustrate the application of the stability criteria to establish the conditions under which a liquid-phase split may occur and the subsequent calculation of liquid-liquid equilibrium using a chemical-theory-modified Flory-Huggins equation to describe the non ideality of aqueous two-phase systems composed of poly(ethylene glycol and dextran. The model was found to be able to correlate ternary liquid-liquid diagrams reasonably well by simple adjustment of the polymer-polymer binary interaction parameter.

  4. Phase-Contrast Imaging of Nanostructures with Incoherent Femtosecond Laser Driven Soft X-Ray Source

    International Nuclear Information System (INIS)

    Application of polychromatic (1.5-15 nm) soft X-ray emission of a spatially large (>0.1 mm) bright femtosecond laser driven plasma source for propagation based phase contrast imaging of nanometer thick foils and biological samples is considered. Diffraction and phase contrast effects increased quality and contrast of the experimental images, registered by LiF crystal X-ray detector with submicron resolution.

  5. X-ray phase imaging with a laboratory source using selective reflection from a mirror.

    Science.gov (United States)

    Pelliccia, Daniele; Paganin, David M

    2013-04-22

    A novel approach for hard x-ray phase contrast imaging with a laboratory source is reported. The technique is based on total external reflection from the edge of a mirror, aligned to intercept only half of the incident beam. The mirror edge thus produces two beams. The refraction x-rays undergo when interacting with a sample placed before the mirror, causes relative intensity variations between direct and reflected beams. Quantitative phase contrast and pure absorption imaging are demonstrated using this method.

  6. RF Phase Stability and Electron Beam Characterization for the PLEIADES Thomson X-Ray Source

    Energy Technology Data Exchange (ETDEWEB)

    Brown, W J; Hartemann, F V; Tremaine, A M; Springer, P T; Le Sage, G P; Barty, C P J; Rosenzweig, J B; Crane, J K; Cross, R R; Fittinghoff, D N; Gibson, D J; Slaughter, D R; Anderson, S

    2002-10-16

    We report on the performance of an S-band RF photocathode electron gun and accelerator for operation with the PLEIADES Thomson x-ray source at LLNL. To produce picosecond, high brightness x-ray pulses, picosecond timing, terahertz bandwidth diagnostics, and RF phase control are required. Planned optical, RF, x-ray and electron beam measurements to characterize the dependence of electron beam parameters and synchronization on RF phase stability are presented.

  7. Visibility in differential phase-contrast imaging with partial coherence source

    Institute of Scientific and Technical Information of China (English)

    Liu Xin; Guo Jin-Chuan; Peng Xiang; Niu Han-Ben

    2007-01-01

    This paper gives theoretical analysis of visibility of fringes, which is influenced by distances, temporal and spatial coherence of source, in hard x-ray differential phase-contrast imaging with microfocus x-ray source. According to the character of longitudinal periodicity of the interferogram, the setup is insensitive to mechanical drift and vibrations. The effect of temporal coherence of x-ray source is investigated and its related bandwidth is derived. Based on the theory of partially coherent light, it shows that the requirement for the spatial coherence of x-ray source is not strict and can be met by the general microfocus x-ray tube for x-ray differential phase-contrast imaging.

  8. Is uracil aromatic? The enthalpies of hydrogenation in the gaseous and crystalline phases, and in aqueous solution, as tools to obtain an answer.

    Science.gov (United States)

    Galvão, Tiago L P; Rocha, Inês M; da Silva, Maria D M C Ribeiro; da Silva, Manuel A V Ribeiro

    2013-07-18

    The enthalpy of hydrogenation of uracil was derived from the experimental enthalpies of formation, in the gaseous phase, of uracil and 5,6-dihydrouracil, in order to analyze its aromaticity. The enthalpy of formation of 5,6-dihydrouracil was obtained from combustion calorimetry, Knudsen effusion technique and Calvet microcalorimetry results. High-level computational methods were tested for the enthalpy of hydrogenation of uracil, but only with G3 was possible to obtain results in agreement with the experimental ones. It was found that uracil possesses 30.0% of aromatic character in the gaseous phase. Using both implicit, explicit, and hybrid solvation methods, it was possible to obtain a reference value for the enthalpy of hydrogenation of uracil in the aqueous solution and the effect of polarity and hydrogen bonds on the aromaticity of uracil was analyzed. The value of the hydrogenation enthalpy of uracil in aqueous solution was compared with the experimental value in the crystal phase, also dominated by polarity and hydrogen bonds, derived from combustion calorimetry results. The supramolecular effects on the crystal lattice were explored by the computational simulation of π-π staking dimers and hydrogen bonded dimers.

  9. Modeling phase equilibria of semiclathrate hydrates of CH4, CO2 and N2 in aqueous solution of tetra-(n)-butyl ammonium bromide

    Institute of Scientific and Technical Information of China (English)

    Abhishek Joshi; Prathyusha Mekala; Jitendra S.Sangwai

    2012-01-01

    Semiclathrate hydrates of tetra-(n)-butyl ammonium bromide (TBAB) offer potential solution for gas storage,transportation,separation of flue gases and CO2 sequestration.Models for phase equilibria for these systems have not yet been developed in open literatures and thus require urgent attention.In this work,the first attempt has been made to model phase equilibria of semiclathrate hydrates of CH4,CO2 and N2 in aqueous solution of TBAB.A thermodynamic model for gas hydrate system as proposed by Chen and Guo has been extended for semiclathrate hydrates of gases in aqueous solution of TBAB.A correlation for the activity of water relating to the system temperature,concentration of TBAB in the system and the nature of guest gas molecule has been proposed.The model results have been validated against available experimental data on phase equilibria of semiclathrate hydrate systems of aqueous TBAB with different gases as guest molecule.The extended Chen and Guo's model is found to be suitable to explain the promotion effect of TBAB for the studied gaseous system such as,methane,carbon dioxide and nitrogen as a guest molecule.Additionally,a correlation for the increase in equilibrium formation temperature (hydrate promotion temperature,△Tp) of semiclathrate hydrate system with respect to pure gas hydrate system has been developed and applied to semiclathrate hydrate of TBAB with several gases as guest molecules.The developed correlation is found to predict the promotion effect satisfactorily for the system studied.

  10. Chemical characterization of SOA formed from aqueous-phase reactions of phenols with the triplet excited state of carbonyl and hydroxyl radical

    Science.gov (United States)

    Yu, L.; Smith, J.; Laskin, A.; Anastasio, C.; Laskin, J.; Zhang, Q.

    2014-12-01

    Phenolic compounds, which are emitted in significant amounts from biomass burning, can undergo fast reactions in atmospheric aqueous phases to form secondary organic aerosol (aqSOA). In this study, we investigate the reactions of phenol (compound with formula C6H5OH)), guaiacol (2-methoxyphenol), and syringol (2,6-dimethoxyphenol) with two major aqueous-phase oxidants - the triplet excited states of an aromatic carbonyl (3C*) and hydroxyl radical (· OH). We thoroughly characterize the low-volatility species produced from these reactions and interpret their formation mechanisms using aerosol mass spectrometry (AMS), nanospray desorption electrospray ionization mass spectrometry (nano-DESI MS), and ion chromatography (IC). A large number of oxygenated molecules are identified, including oligomers containing up to six monomer units, functionalized monomer and oligomers with carbonyl, carboxyl, and hydroxyl groups, and small organic acid anions (e.g., formate, acetate, oxalate, and malate). The average atomic oxygen-to-carbon (O / C) ratios of phenolic aqSOA are in the range of 0.85-1.23, similar to those of low-volatility oxygenated organic aerosol (LV-OOA) observed in ambient air. The aqSOA compositions are overall similar for the same precursor, but the reactions mediated by 3C* are faster than · OH-mediated reactions and produce more oligomers and hydroxylated species at the point when 50% of the phenolic compound has reacted. Profiles determined using a thermodenuder indicate that the volatility of phenolic aqSOA is influenced by both oligomer content and O / C ratio. In addition, the aqSOA shows enhanced light absorption in the UV-visible region, suggesting that aqueous-phase reactions of phenols may contribute to formation of secondary brown carbon in the atmosphere, especially in regions influenced by biomass burning.

  11. Power Controllability of Three-phase Converter with Unbalanced AC Source

    DEFF Research Database (Denmark)

    Ma, Ke; Liserre, Marco; Blaabjerg, Frede

    2013-01-01

    Three-phase DC-AC power converters suffer from power oscillation and overcurrentt problems in case of unbalanced AC source voltage that can be caused by grid/generator faults. Existing solutions to handle these problems are properly selecting and controlling the positive and negative sequence...... converter can enable more flexible control targets, achieving better performances in the delivered power and load current when suffering from unbalanced AC sources....

  12. Carrier phase shifted SPWM based on current sourced multi-modular converter for active power filter

    Institute of Scientific and Technical Information of China (English)

    王立乔; 李建林; 张仲超

    2004-01-01

    A novel current-source active power filter(APF)based on multi-modular converter with carrier phase-shifted SPWM(CPS-SPWM)technique is proposed.With this technique,the effect of equivalent high switching frequency converter is obtained with low switching frequency converter.It is very promising in current-source APF that adopt superconducting magnetic energy storage component.

  13. 28 MHz swept source at 1.0 μm for ultrafast quantitative phase imaging

    OpenAIRE

    Wei, Xiaoming; Lau, Andy K. S.; Xu, Yiqing; Tsia, Kevin K.; Wong, Kenneth K. Y.

    2015-01-01

    Emerging high-throughput optical imaging modalities, in particular those providing phase information, necessitate a demanding speed regime (e.g. megahertz sweep rate) for those conventional swept sources; while an effective solution is yet to be demonstrated. We demonstrate a stable breathing laser as inertia-free swept source (BLISS) operating at a wavelength sweep rate of 28 MHz, particularly for the ultrafast interferometric imaging modality at 1.0 μm. Leveraging a tunable dispersion compe...

  14. Characterizing Fullerene Nanoparticles in Aqueous Suspensions

    Science.gov (United States)

    Studies have indicated that fullerenes can form stable colloidal suspensions in water when introduced to the aqueous phase through solvent exchange, sonication, or extended mixing. The colloidal suspensions created using these techniques have effective aqueous phase concentratio...

  15. Melting of a phase change material in a horizontal annulus with discrete heat sources

    Directory of Open Access Journals (Sweden)

    Mirzaei Hooshyar

    2015-01-01

    Full Text Available Phase change materials have found many industrial applications such as cooling of electronic devices and thermal energy storage. This paper investigates numerically the melting process of a phase change material in a two-dimensional horizontal annulus with different arrangements of two discrete heat sources. The sources are positioned on the inner cylinder of the annulus and assumed as constant-temperature boundary conditions. The remaining portion of the inner cylinder wall as well as the outer cylinder wall is considered to be insulated. The emphasis is mainly on the effects of the arrangement of the heat source pair on the fluid flow and heat transfer features. The governing equations are solved on a non-uniform O type mesh using a pressure-based finite volume method with an enthalpy porosity technique to trace the solid and liquid interface. The results are obtained at Ra=104 and presented in terms of streamlines, isotherms, melting phase front, liquid fraction and dimensionless heat flux. It is observed that, depending on the arrangement of heat sources, the liquid fraction increases both linearly and non-linearly with time but will slow down at the end of the melting process. It can also be concluded that proper arrangement of discrete heat sources has the great potential in improving the energy storage system. For instance, the arrangement C3 where the heat sources are located on the bottom part of the inner cylinder wall can expedite the melting process as compared to the other arrangements.

  16. A plant-wide aqueous phase chemistry module describing pH variations and ion speciation/pairing in wastewater treatment process models

    DEFF Research Database (Denmark)

    Flores Alsina, Xavier; Kazadi Mbamba, Christian; Solon, Kimberly;

    2015-01-01

    , but unavoidable, additional degree of complexity when representing cationic/anionic behaviour in Activated Sludge (AS)/Anaerobic Digestion (AD) systems. In this paper, a plant-wide aqueous phase chemistry module describing pH variations plus ion speciation/pairing is presented and interfaced with industry......) in order to reduce the overall stiffness of the system, thereby enhancing simulation speed. Additionally, a multi-dimensional version of the Newton-Raphson algorithm is applied to handle the existing multiple algebraic inter-dependencies. The latter is reinforced with the Simulated Annealing method...

  17. Influence of NO2 and metal ions on oxidation of aqueous-phase S(IV in atmospheric concentrations

    Directory of Open Access Journals (Sweden)

    Cláudia R. Martins

    2008-06-01

    Full Text Available An investigation was made of the influence of atmospheric concentrations (15 or 130 ppbv of NO2 on the aqueous-phase oxidation rate of S(IV in the presence and absence of Fe(III, Mn(II and Cr(VI metal ions under controlled experimental conditions (pH, T, concentration of reactants, etc.. The reaction rate in the presence of the NO2 flow was slower than the reaction rate using only clean air with an initial S(IV concentration of 10-4 mol/L. NO2 appears to react with S(IV, producing a kind of inhibitor that slows down the reaction. Conversely, tenfold lower concentrations of S(IV ([S(IV]º = 10-5 mol/L caused a faster reaction in the presence of NO2 than the reaction using purified air. Under these conditions, therefore, the equilibrium shifts to sulfate formation. With the addition of Fe(III, Mn(II or Cr(VI in the presence of a NO2 flow, the reaction occurred faster under all the conditions in which S(IV oxidation was investigated.A reação de oxidação de S(IV em fase aquosa foi estudada em laboratório em presença de NO2 dos íons metálicos Fe(III, Mn(II, e Cr(VI sob condições experimentais controladas (pH, T, concentração dos reagentes, etc.. Na presença de corrente de ar com NO2 (15 ou 130 ppbv a reação de oxidação de S(IV ocorreu mais lentamente do que na presença de ar purificado, para uma concentração inicial de S(IV de 10-4 mol/L. Ao contrário, para concentração inicial de S(IV dez vezes menor ([S(IV]° = 10-5 mol/L a reação ocorreu mais rapidamente na presença de NO2. A explicação está relacionada com o equilíbrio envolvendo a formação de espécies intermediárias de longa vida, que impedem o prosseguimento da reação, porém a depender das concentrações relativas de S(IV e NO2, essas espécies se decompõem deslocando o equilíbrio no sentido de formação de sulfato. A adição dos íons Fe(III, Mn(II ou Cr(VI em presença de corrente de ar com NO2 indicou atividade catalítica para esses íons, em todas

  18. Liquid-Phase Synthesis of Ba2V2O7 Phosphor Powders and Films Using Immiscible Biphasic Organic-Aqueous Systems.

    Science.gov (United States)

    Takahashi, Mami; Hagiwara, Manabu; Fujihara, Shinobu

    2016-08-15

    A liquid-phase synthesis of inorganic phosphor materials at a moderate temperature was proposed by using immiscible liquid-liquid biphasic systems. A self-activated Ba2V2O7 phosphor was actually synthesized from vanadium alkoxide dissolved in an organic solution and barium acetate in an aqueous solution. A mild hydrolysis reaction of the alkoxide started at the organic-inorganic interface, and an intermediate compound, Ba(VO3)2·H2O, was initially formed. Ba2V2O7 powders were then obtained by the conversion from Ba(VO3)2·H2O promoted in the aqueous solution. Ba2V2O7 films were obtained on surface-modified silica glass substrates through the similar chemical reactions. Factors such as the surface state of substrates, the kind of organic solvents, and the volume of aqueous solutions were examined to improve the film deposition behavior. The resultant Ba2V2O7 materials showed broad-band visible photoluminescence upon irradiation with ultraviolet light based on the charge transfer transition in the VO4(3-) units existing as dimers. PMID:27472450

  19. Liquid-Phase Synthesis of Ba2V2O7 Phosphor Powders and Films Using Immiscible Biphasic Organic-Aqueous Systems.

    Science.gov (United States)

    Takahashi, Mami; Hagiwara, Manabu; Fujihara, Shinobu

    2016-08-15

    A liquid-phase synthesis of inorganic phosphor materials at a moderate temperature was proposed by using immiscible liquid-liquid biphasic systems. A self-activated Ba2V2O7 phosphor was actually synthesized from vanadium alkoxide dissolved in an organic solution and barium acetate in an aqueous solution. A mild hydrolysis reaction of the alkoxide started at the organic-inorganic interface, and an intermediate compound, Ba(VO3)2·H2O, was initially formed. Ba2V2O7 powders were then obtained by the conversion from Ba(VO3)2·H2O promoted in the aqueous solution. Ba2V2O7 films were obtained on surface-modified silica glass substrates through the similar chemical reactions. Factors such as the surface state of substrates, the kind of organic solvents, and the volume of aqueous solutions were examined to improve the film deposition behavior. The resultant Ba2V2O7 materials showed broad-band visible photoluminescence upon irradiation with ultraviolet light based on the charge transfer transition in the VO4(3-) units existing as dimers.

  20. A multi-phase level set framework for source reconstruction in bioluminescence tomography

    International Nuclear Information System (INIS)

    We propose a novel multi-phase level set algorithm for solving the inverse problem of bioluminescence tomography. The distribution of unknown interior source is considered as piecewise constant and represented by using multiple level set functions. The localization of interior bioluminescence source is implemented by tracing the evolution of level set function. An alternate search scheme is incorporated to ensure the global optimal of reconstruction. Both numerical and physical experiments are performed to evaluate the developed level set reconstruction method. Reconstruction results show that the proposed method can stably resolve the interior source of bioluminescence tomography.

  1. A microdevice assisted approach for the preparation, characterization and selection of continuous aqueous two-phase systems: from micro to bench-scale.

    Science.gov (United States)

    Vázquez-Villegas, Patricia; Ouellet, Eric; González, Claudia; Ruiz-Ruiz, Federico; Rito-Palomares, Marco; Haynes, Charles A; Aguilar, Oscar

    2016-07-01

    Aqueous two-phase systems (ATPS) have emerged as an alternative strategy for the recovery and purification of a wide variety of biological products. Typical process development requires a large screening of experimental conditions towards industrial adoption where continuous processes are preferred. In this work, it was proved that under certain flow conditions, ATPS could be formed continuously inside a microchannel, starting from stocks of phase components. Staggered herringbone chaotic micromixers included within the device sequentially and rapidly prepare two-phase systems across an entire range of useful phase compositions. Two-phase diagrams (binodal curves) were easily plotted using the cloud-point method for systems of different components and compared with previously reported curves for each system, proving that phase formation inside the device correlated with the previously reported diagrams. A proof of concept for sample partitioning in such a microdevice was performed with two different experimental models: BSA and red blood cells. Finally, the microdevice was employed to obtain information about the recovery and partition coefficient of invertase from a real complex mixture of proteins (yeast extract) to design a process for the recovery of the enzyme selecting a suitable system and composition to perform the process at bench-scale. PMID:27302418

  2. An Integrated Inductor For Parallel Interleaved Three-Phase Voltage Source Converters

    DEFF Research Database (Denmark)

    Gohil, Ghanshyamsinh Vijaysinh; Bede, Lorand; Teodorescu, Remus;

    2016-01-01

    Three phase Voltage Source Converters (VSCs) are often connected in parallel to realize high current output converter system. The harmonic quality of the resultant switched output voltage can be improved by interleaving the carrier signals of these parallel connected VSCs. As a result, the line...

  3. Revisiting source identification, weathering models, and phase discrimination for Exxon Valdez oil

    Energy Technology Data Exchange (ETDEWEB)

    Driskell, W.B.; Payne, J.R. [Payne Environmental Consultants Inc., Encinitas, CA (United States); Shigenaka, G. [National Oceanic and Atmospheric Administration, Seattle, WA (United States)

    2005-07-01

    A large chemistry data set for polycyclic aromatic hydrocarbon (PAH) and saturated hydrocarbon (SHC) contamination in sediment, water and tissue samples has emerged in the aftermath of the 1989 Exxon Valdez oil spill in Prince William Sound, Alaska. When the oil was fresh, source identification was a primary objective and fairly reliable. However, source identification became problematic as the oil weathered and its signatures changed. In response to concerns regarding when the impacted area will be clean again, this study focused on developing appropriate tools to confirm hydrocarbon source identifications and assess weathering in various matrices. Previous efforts that focused only on the whole or particulate-phase oil are not adequate to track dissolved-phase signal with low total PAH values. For that reason, a particulate signature index (PSI) and dissolved signature index (DSI) screening tool was developed in this study to discriminate between these 2 phases. The screening tool was used to measure the dissolved or water-soluble fraction of crude oil which occurs at much lower levels than the particulate phase, but which is more widely circulated and equally as important as the particulate oil phase. The discrimination methods can also identify normally-discarded, low total PAH samples which can increase the amount of usable data needed to model other effects of oil spills. 37 refs., 3 tabs., 10 figs.

  4. 采用特殊的相反转乳化剂制备水基环氧固化剂分散体%Preparation of aqueous dispersion of epoxy curing agent with specially synthesized phase inversion emulsifier

    Institute of Scientific and Technical Information of China (English)

    周继亮; 涂伟萍; 胡剑青

    2005-01-01

    Generally, the curing agents for aqueous ambient-temperature-cured epoxy resin systems are epoxy-polyamine adduct, which are rendered water-soluble by salting with organic acids,while these acids have adverse influence on film property.It is a trend to develop aqueous dispersion of epoxy curing agent free of organic acids.The conventional surfactants are not suited to act as phase inversion emulsifiers to prepare aqueous dispersion of epoxy-polyamine adduct. So a special phase inversion emulsifier TETA-DGEPG-EPON834 was synthesized in two steps.Firstly, diglycidyl ether of polyglycol(DGEPG) was used as the chain extender to react with triethylenete tramine(TETA) in propylene glycol methyl ether (PM) at 70℃ for about 4 h.Secondly, epoxy resin(EPON834) was used as the chain extender to react with the adduct of TETA-DGEPG in PM at 65℃ for about 3 h.Then the special phase inversion emulsifier was used to prepare aqueous dispersion of EPON828-TETA adduct terminated by E10. In circumstances of low emulsifier concentration (5%), phase inversion was not completed at phase inversion point (PIP) (0.35). While the phase inversion has completely finished at PIP (0.45) in the circumstances of high emulsifier concentration (10%).A stable aqueous dispersion of EPON828-TETA adduct terminated by E10 was prepared in circumstances of high emulsifier concentration (10%).

  5. A database of phase calibration sources and their radio spectra for the Giant Metrewave Radio Telescope

    Science.gov (United States)

    Lal, Dharam V.; Dubal, Shilpa S.; Sherkar, Sachin S.

    2016-10-01

    We are pursuing a project to build a database of phase calibration sources suitable for Giant Metrewave Radio Telescope (GMRT). Here we present the first release of 45 low frequency calibration sources at 235 MHz and 610 MHz. These calibration sources are broadly divided into quasars, radio galaxies and unidentified sources. We provide their flux densities, models for calibration sources, (u,v) plots, final deconvolved restored maps and uc(clean)-component lists/files for use in the Astronomical Image Processing System (uc(aips)) and the Common Astronomy Software Applications (uc(casa)). We also assign a quality factor to each of the calibration sources. These data products are made available online through the GMRT observatory website. In addition we find that (i) these 45 low frequency calibration sources are uniformly distributed in the sky and future efforts to increase the size of the database should populate the sky further, (ii) spectra of these calibration sources are about equally divided between straight, curved and complex shapes, (iii) quasars tend to exhibit flatter radio spectra as compared to the radio galaxies or the unidentified sources, (iv) quasars are also known to be radio variable and hence possibly show complex spectra more frequently, and (v) radio galaxies tend to have steeper spectra, which are possibly due to the large redshifts of distant galaxies causing the shift of spectrum to lower frequencies.

  6. GPU-based Monte Carlo radiotherapy dose calculation using phase-space sources

    CERN Document Server

    Townson, Reid; Tian, Zhen; Graves, Yan Jiang; Zavgorodni, Sergei; Jiang, Steve B

    2013-01-01

    A novel phase-space source implementation has been designed for GPU-based Monte Carlo dose calculation engines. Due to the parallelized nature of GPU hardware, it is essential to simultaneously transport particles of the same type and similar energies but separated spatially to yield a high efficiency. We present three methods for phase-space implementation that have been integrated into the most recent version of the GPU-based Monte Carlo radiotherapy dose calculation package gDPM v3.0. The first method is to sequentially read particles from a patient-dependent phase-space and sort them on-the-fly based on particle type and energy. The second method supplements this with a simple secondary collimator model and fluence map implementation so that patient-independent phase-space sources can be used. Finally, as the third method (called the phase-space-let, or PSL, method) we introduce a novel strategy to pre-process patient-independent phase-spaces and bin particles by type, energy and position. Position bins l...

  7. Separation of clavulanic acid from fermented broth of amino acids by an aqueous two-phase system and ion-exchange adsorption.

    Science.gov (United States)

    da Silva, Clovis Sacardo; Cuel, Maressa Fabiano; Barreto, Verônica Orlandin; Kwong, Wu Hong; Hokka, Carlos O; Barboza, M

    2012-02-15

    The clavulanic acid is a substance which inhibits the β-lactamases used with penicillins for therapeutic treatment. After the fermentation, by-products of low molecular weight such as amino acids lysine, histidine, proline and tyrosine are present in the fermented broth. To remove these impurities the techniques of extraction by an aqueous two-phase system of 17% polyethylene glycol molecular weight 600 and 15% potassium phosphate were used for a partial purification. A subsequent ion-exchange adsorption was used for the recuperation of the clavulanic acid of the top phase and purification getting a concentration factor of 2 and purification of 100% in relation to the amino acids lysine, histidine, proline and tyrosine.

  8. Determination of Aroma Compound Partition Coefficients in Aqueous, Polysaccharide, and Dairy Matrices Using the Phase Ratio Variation Method: A Review and Modeling Approach.

    Science.gov (United States)

    Heilig, Andrej; Sonne, Alina; Schieberle, Peter; Hinrichs, Jörg

    2016-06-01

    The partition of aroma compounds between a matrix and a gas phase describes an individual compound's specific affinity toward the matrix constituents affecting orthonasal sensory perception. The static headspace phase ratio variation (PRV) method has been increasingly applied by various authors to determine the equilibrium partition coefficient K in aqueous, polysaccharide, and dairy matrices. However, reported partition coefficients are difficult to relate and compare due to different experimental conditions, e.g., aroma compound selection, matrix composition, equilibration temperature. Due to its specific advantages, the PRV method is supposed to find more frequent application in the future, this Review aims to summarize, evaluate, compare, and relate the currently available data on PRV-determined partition coefficients. This process was designed to specify the potentials and the limitations as well as the consistency of the PRV method, and to identify open fields of research in aroma compound partitioning in food-related, especially dairy matrices. PMID:27182770

  9. Aqueous phase synthesis of upconversion nanocrystals through layer-by-layer epitaxial growth for in vivo X-ray computed tomography

    KAUST Repository

    Li, Feifei

    2013-05-21

    Lanthanide-doped core-shell upconversion nanocrystals (UCNCs) have tremendous potential for applications in many fields, especially in bio-imaging and medical therapy. As core-shell UCNCs are mostly synthesized in organic solvents, tedious organic-aqueous phase transfer processes are usually needed for their use in bio-applications. Herein, we demonstrate the first example of one-step synthesis of highly luminescent core-shell UCNCs in the "aqueous" phase under mild conditions using innocuous reagents. A microwave-assisted approach allowed for layer-by-layer epitaxial growth of a hydrophilic NaGdF4 shell on NaYF4:Yb, Er cores. During this process, surface defects of the nanocrystals could be gradually passivated by the homogeneous shell deposition, resulting in obvious enhancement in the overall upconversion emission efficiency. In addition, the up-down conversion dual-mode luminescent NaYF4:Yb, Er@NaGdF4:Ce, Ln (Eu, Tb, Sm, Dy) nanocrystals were also synthesized to further validate the successful formation of the core-shell structure. More significantly, based on their superior solubility and stability in water solution, high upconversion efficiency and Gd-doped predominant X-ray absorption, the as-prepared NaYF4:Yb, Er@NaGdF4 core-shell UCNCs exhibited high contrast in in vitro cell imaging and in vivo X-ray computed tomography (CT) imaging, demonstrating great potential as multiplexed luminescent biolabels and CT contrast agents.

  10. Growth mechanism of a gas clathrate hydrate from a dilute aqueous gas solution: a molecular dynamics simulation of a three-phase system.

    Science.gov (United States)

    Nada, Hiroki

    2006-08-24

    A molecular dynamics simulation of a three-phase system including a gas clathrate, liquid water, and a gas was carried out at 298 K and high pressure in order to investigate the growth mechanism of the clathrate from a dilute aqueous gas solution. The simulation indicated that the clathrate grew on interfaces between the clathrate and the liquid water, after transfer of the gas molecules from the gas phase to the interfaces. The results suggest a two-step process for growth: first, gas molecules are arranged at cage sites, and second, H(2)O molecules are ordered near the gas molecules. The results also suggest that only the H(2)O molecules, which are surrounded or sandwiched by the gas molecules, form the stable polygons that constitute the cages of the clathrate. In addition, the growth of the clathrate from a concentrated aqueous gas solution was also simulated, and the results suggested a growth mechanism in which many H(2)O and gas molecules correctively form the structure of the clathrate. The clathrate grown from the concentrated solution contained some empty cages, whereas the formation of empty cages was not observed during the growth from the dilute solution. The results obtained by both simulations are compared with the results of an experimental study, and the growth mechanism of the clathrate in a real system is discussed.

  11. Liquid chromatography/tandem mass spectrometric bioanalysis using normal-phase columns with aqueous/organic mobile phases - a novel approach of eliminating evaporation and reconstitution steps in 96-well SPE.

    Science.gov (United States)

    Naidong, Weng; Shou, Wilson Z; Addison, Thomas; Maleki, Saber; Jiang, Xiangyu

    2002-01-01

    Bioanalytical methods using automated 96-well solid-phase extraction (SPE) and liquid chromatography with electrospray tandem mass spectrometry (LC/MS/MS) are widely used in the pharmaceutical industry. SPE methods typically require manual steps of drying of the eluates and reconstituting of the analytes with a suitable injection solvent possessing elution strength weaker than the mobile phase. In this study, we demonstrated a novel approach of eliminating these two steps in 96-well SPE by using normal-phase LC/MS/MS methods with low aqueous/high organic mobile phases, which consisted of 70-95% organic solvent, 5-30% water, and small amount of volatile acid or buffer. While the commonly used SPE elution solvents (i.e. acetonitrile and methanol) have stronger elution strength than a mobile phase on reversed-phase chromatography, they are weaker elution solvents than a mobile phase for normal-phase LC/MS/MS and therefore can be injected directly. Analytical methods for a range of polar pharmaceutical compounds, namely, omeprazole, metoprolol, fexofenadine, pseudoephedrine as well as rifampin and its metabolite 25-desacetyl-rifampin, in biological fluids, were developed and optimized based on the foregoing principles. As a result of the time saving, a batch of 96 samples could be processed in one hour. These bioanalytical LC/MS/MS methods were validated according to "Guidance for Industry - Bioanalytical Method Validation" recommended by the Food and Drug Administration (FDA) of the United States.

  12. Separation of Cd and Ni from Ni-Cd batteries by an environmentally safe methodology employing aqueous two-phase systems

    Energy Technology Data Exchange (ETDEWEB)

    Lacerda, Vania Goncalves; Mageste, Aparecida Barbosa; Santos, Igor Jose Boggione; da Silva, Luis Henrique Mendes; da Silva, Maria do Carmo Hespanhol [Grupo de Quimica Verde Coloidal e Macromolecular, Departamento de Quimica, Centro de Ciencias e Tecnologicas, Universidade Federal de Vicosa, Av. P.H. Rolfs s/n, Campus da UFV, Vicosa, 36570-000 (Brazil)

    2009-09-05

    The separation of Cd and Ni from Ni-Cd batteries using an aqueous two-phase system (ATPS) composed of copolymer L35, Li{sub 2}SO{sub 4} and water is investigated. The extraction behavior of these metals from the bottom phase (BP) to the upper phase (UP) of the ATPS is affected by the amount of added extractant (potassium iodide), tie-line length (TLL), mass ratio between the phases of the ATPS, leaching and dilution factor of the battery samples. Maximum extraction of Cd (99.2 {+-} 3.1)% and Ni (10.6 {+-} 0.4)% is obtained when the batteries are leached with HCl, under the following conditions: 62.53% (w/w) TLL, concentration of KI equal to 50.00 mmol kg{sup -1}, mass ratio of the phases equal to 0.5 and a dilution factor of battery samples of 35. This novel methodology is efficient to separate the metals in question, with the advantage of being environmentally safe, since water is the main constituent of the ATPS, which is prepared with recyclable and biodegradable compounds. (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. The source vector and static displacement field by elastic dislocation on the two-phase saturated medium

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Based on the Biot's theory about two-phase saturated medium, according to the character of d function, the Green function on two-phase saturated medium by the point source under concentrated force can be derived. By the Betti's theorem for the two-phase saturated medium field, the source vector and static displacement field by elastic dislocation on the two-phase saturated medium were comprehensively discussed.

  15. CdTe quantum dots: aqueous phase synthesis, stability studies and protein conjugation for development of biosensors

    Science.gov (United States)

    Borse, Vivek; Sadawana, Mayur; Srivastava, Rohit

    2016-04-01

    Synthesis of quantum dots (QDs) in aqueous medium is advantageous as compared to the organic solvent mediated synthesis, as the aqueous synthesis is less toxic, reagent effective, easily reproducible and importantly, synthesized QDs have biological compatibility. The QDs should be aqueous in nature for use in cell imaging, drug labeling, tracking and delivery. Structural modifications are necessary to enable their use in biosensing application. In this work, mercaptopropionic acid capped cadmium telluride QDs (MPA-CdTe QDs) were synthesized by hydrothermal method and characterized by various techniques. Water and various biochemical buffers were used to study the fluorescence intensity stability of the QDs at different physicochemical conditions. QDs stored in 4° C showed excellent stability of fluorescence intensity values as compared to the samples stored at room temperature. Staphylococcal protein A (SPA) was conjugated with the QDs (SPA-QDs) and characterized using UV and fluorescence spectroscopy, zeta potential, HRTEM, FTIR, and AFM. Blue shift was observed in the fluorescence emission spectra that may be due to reduction in the surface charge as carboxyl groups on QDs were replaced by amino groups of SPA. This SPA conjugated to QDs enables binding of the C-terminal of antibodies on its surface allowing N-terminal binding site remain free to bind with antigenic biomarkers. Thus, the biosensor i.e. antibody bound on SPA-QDs would bind to the antigenic biomarkers in sample and the detection system could be developed. As QDs have better fluorescence properties than organic dyes, this biosensor will provide high sensitivity and quantitative capability in diagnostics.

  16. Study of the imaging property of a fluorescent confocal microscopy with a phase-only filter in an extended source

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The phase information of an enlarged source is reconstructed with an annular two-zone phase-only filter in a fluorescent confocal scanning optical microscope for resolution improvement. The dependences of its resolution on the source size and on the phase transmission of the outer annular zone of the filter are investigated theoretically by use of its three-dimensional optical transfer function (3D OTF ). The increased source size and the required phase value of the outer annular zone of the phase-only filter for an optimal 3D OTF of the optical system are presented.

  17. Investigation on a Novel Discontinuous Pulse-Width Modulation Algorithm for Single-phase Voltage Source Rectifier

    DEFF Research Database (Denmark)

    Qu, Hao; Yang, Xijun; Guo, Yougui;

    2014-01-01

    Single-phase voltage source converter (VSC) is an important power electronic converter (PEC), including single-phase voltage source inverter (VSI), single-phase voltage source rectifier (VSR), single-phase active power filter (APF) and single-phase grid-connection inverter (GCI). Single-phase VSC...... as well as its modulation algorithms is widely used as the fundamental part of large scale PEC’s, having a long list of applications. In the paper, as first, on the basis of the discontinuous pulse-width modulation (DPWM) of three-phase VSC, a new DPWM of single-phase VSR is presented in virtue of...... zero-sequence component injection, in order to reduce power loss and increased overall efficiency. And then by reconstructing the other two phase input voltages and currents, the transformation from stationary frame (abc) to rotating frame (dq frame) is designed. Finally, a PI regulator based...

  18. W phase source inversion for moderate to large earthquakes (1990-2010)

    Science.gov (United States)

    Duputel, Zacharie; Rivera, Luis; Kanamori, Hiroo; Hayes, Gavin P.

    2012-01-01

    Rapid characterization of the earthquake source and of its effects is a growing field of interest. Until recently, it still took several hours to determine the first-order attributes of a great earthquake (e.g. Mw≥ 7.5), even in a well-instrumented region. The main limiting factors were data saturation, the interference of different phases and the time duration and spatial extent of the source rupture. To accelerate centroid moment tensor (CMT) determinations, we have developed a source inversion algorithm based on modelling of the W phase, a very long period phase (100–1000 s) arriving at the same time as the P wave. The purpose of this work is to finely tune and validate the algorithm for large-to-moderate-sized earthquakes using three components of W phase ground motion at teleseismic distances. To that end, the point source parameters of all Mw≥ 6.5 earthquakes that occurred between 1990 and 2010 (815 events) are determined using Federation of Digital Seismograph Networks, Global Seismographic Network broad-band stations and STS1 global virtual networks of the Incorporated Research Institutions for Seismology Data Management Center. For each event, a preliminary magnitude obtained from W phase amplitudes is used to estimate the initial moment rate function half duration and to define the corner frequencies of the passband filter that will be applied to the waveforms. Starting from these initial parameters, the seismic moment tensor is calculated using a preliminary location as a first approximation of the centroid. A full CMT inversion is then conducted for centroid timing and location determination. Comparisons with Harvard and Global CMT solutions highlight the robustness of W phase CMT solutions at teleseismic distances. The differences in Mw rarely exceed 0.2 and the source mechanisms are very similar to one another. Difficulties arise when a target earthquake is shortly (e.g. within 10 hr) preceded by another large earthquake, which disturbs the

  19. Soft-tissue phase-contrast tomography with an x-ray tube source

    International Nuclear Information System (INIS)

    We report the first experimental soft-tissue phase-contrast tomography results using a conventional x-ray tube source, with a millimeter-sized focal spot. The setup is based on a Talbot-Lau grating interferometer operated at a mean energy of 28 keV. We present three-dimensional ex vivo images of a chicken heart sample, fixated in formalin. The results clearly demonstrate the advantageous contrast attainable through phase-contrast imaging over conventional attenuation-based approaches.

  20. RadSTraM: Radiological Source Tracking and Monitoring, Phase II Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Warren, Tracy A [ORNL; Walker, Randy M [ORNL; Hill, David E [ORNL; Gross, Ian G [ORNL; Smith, Cyrus M [ORNL; Abercrombie, Robert K [ORNL

    2008-12-01

    This report focuses on the technical information gained from the Radiological Source Tracking and Monitoring (RadSTraM) Phase II investigation and its implications. The intent of the RadSTraM project was to determine the feasibility of tracking radioactive materials in commerce, particularly International Atomic Energy Agency (IAEA) Category 3 and 4 materials. Specifically, Phase II of the project addressed tracking radiological medical isotopes in commerce. These categories of materials are susceptible to loss or theft but the problem is not being addressed by other agencies.

  1. Primary and secondary organic aerosol origin by combined gas-particle phase source apportionment

    Directory of Open Access Journals (Sweden)

    M. Crippa

    2013-08-01

    Full Text Available Secondary organic aerosol (SOA, a prominent fraction of particulate organic mass (OA, remains poorly constrained. Its formation involves several unknown precursors, formation and evolution pathways and multiple natural and anthropogenic sources. Here a combined gas-particle phase source apportionment is applied to wintertime and summertime data collected in the megacity of Paris in order to investigate SOA origin during both seasons. This was possible by combining the information provided by an aerosol mass spectrometer (AMS and a proton transfer reaction mass spectrometer (PTR-MS. A better constrained apportionment of primary OA (POA sources is also achieved using this methodology, making use of gas-phase tracers. These tracers made possible the discrimination between biogenic and continental/anthropogenic sources of SOA. We found that continental SOA was dominant during both seasons (24–50% of total OA, while contributions from photochemistry-driven SOA (9% of total OA and marine emissions (13% of total OA were also observed during summertime. A semi-volatile nighttime component was also identified (up to 18% of total OA during wintertime. This approach was successfully applied here and implemented in a new source apportionment toolkit.

  2. Phase contrast tomography of the mouse cochlea at microfocus x-ray sources

    Energy Technology Data Exchange (ETDEWEB)

    Bartels, Matthias; Krenkel, Martin [Institute for X-Ray Physics, University of Göttingen, Göttingen (Germany); Hernandez, Victor H. [InnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, Göttingen (Germany); Bernstein Focus for Neurotechnology, University of Göttingen, Göttingen (Germany); Moser, Tobias [InnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, Göttingen (Germany); Bernstein Focus for Neurotechnology, University of Göttingen, Göttingen (Germany); Center for Nanoscopy and Molecular Physiology of the Brain, Göttingen (Germany); Salditt, Tim [Institute for X-Ray Physics, University of Göttingen, Göttingen (Germany); Center for Nanoscopy and Molecular Physiology of the Brain, Göttingen (Germany)

    2013-08-19

    We present phase contrast x-ray tomography of functional soft tissue within the bony cochlear capsule of mice, carried out at laboratory microfocus sources with well-matched source, detector, geometry, and reconstruction algorithms at spatial resolutions down to 2 μm. Contrast, data quality and resolution enable the visualization of thin membranes and nerve fibers as well as automated segmentation of surrounding bone. By complementing synchrotron radiation imaging techniques, a broad range of biomedical applications becomes possible as demonstrated for optogenetic cochlear implant research.

  3. Enantioseparation of Racemic Flurbiprofen by Aqueous Two-Phase Extraction With Binary Chiral Selectors of L-dioctyl Tartrate and L-tryptophan.

    Science.gov (United States)

    Chen, Zhi; Zhang, Wei; Wang, Liping; Fan, Huajun; Wan, Qiang; Wu, Xuehao; Tang, Xunyou; Tang, James Z

    2015-09-01

    A novel method for chiral separation of flurbiprofen enantiomers was developed using aqueous two-phase extraction (ATPE) coupled with biphasic recognition chiral extraction (BRCE). An aqueous two-phase system (ATPS) was used as an extracting solvent which was composed of ethanol (35.0% w/w) and ammonium sulfate (18.0% w/w). The chiral selectors in ATPS for BRCE consideration were L-dioctyl tartrate and L-tryptophan, which were screened from amino acids, β-cyclodextrin derivatives, and L-tartrate esters. Factors such as the amounts of L-dioctyl tartrate and L-tryptophan, pH, flurbiprofen concentration, and the operation temperature were investigated in terms of chiral separation of flurbiprofen enantiomers. The optimum conditions were as follows: L-dioctyl tartrate, 80 mg; L-tryptophan, 40 mg; pH, 4.0; flurbiprofen concentration, 0.10 mmol/L; and temperature, 25 °C. The maximum separation factor α for flurbiprofen enantiomers could reach 2.34. The mechanism of chiral separation of flurbiprofen enantiomers is discussed and studied. The results showed that synergistic extraction has been established by L-dioctyl tartrate and L-tryptophan, which enantioselectively recognized R- and S-enantiomers in top and bottom phases, respectively. Compared to conventional liquid-liquid extraction, ATPE coupled with BRCE possessed higher separation efficiency and enantioselectivity without the use of any other organic solvents. The proposed method is a potential and powerful alternative to conventional extraction for separation of various enantiomers.

  4. Using Bayesian Belief Network (BBN) modelling for Rapid Source Term Prediction. RASTEP Phase 1

    Energy Technology Data Exchange (ETDEWEB)

    Knochenhauer, M.; Swaling, V.H.; Alfheim, P. [Scandpower AB, Sundbyberg (Sweden)

    2012-09-15

    The project is connected to the development of RASTEP, a computerized source term prediction tool aimed at providing a basis for improving off-site emergency management. RASTEP uses Bayesian belief networks (BBN) to model severe accident progression in a nuclear power plant in combination with pre-calculated source terms (i.e., amount, timing, and pathway of released radio-nuclides). The output is a set of possible source terms with associated probabilities. In the NKS project, a number of complex issues associated with the integration of probabilistic and deterministic analyses are addressed. This includes issues related to the method for estimating source terms, signal validation, and sensitivity analysis. One major task within Phase 1 of the project addressed the problem of how to make the source term module flexible enough to give reliable and valid output throughout the accident scenario. Of the alternatives evaluated, it is recommended that RASTEP is connected to a fast running source term prediction code, e.g., MARS, with a possibility of updating source terms based on real-time observations. (Author)

  5. The Investigation of Sinusoidal Single Phase Voltage Source Inverter Output Filter

    Directory of Open Access Journals (Sweden)

    Andrius Platakis

    2011-08-01

    Full Text Available The results of output filter investigation of single phase sine voltage source inverter (VSI are presented. The operating principle, construction and a most widely used topology of single phase voltage source inverter is discussed. The results obtained using modeling and experimental investigation are presented. The Total Harmonic Distortion of the inverter output voltage and maximal current of the output capacitor were analyzed using Matlab Simulink software. The 1 kW inverter prototype was built for experimental investigation. The inverter switches are realized using IGBT transistors. The toroidal iron powder core with distributed air gap was used as the core of the inductor. The experimental investigation of inductor core losses and maximal current of output filter capacitor were performed.Article in Lithuanian

  6. Power Controllability of Three-phase Converter with Unbalanced AC Source

    DEFF Research Database (Denmark)

    Ma, Ke; Chen, Wenjie; Liserre, Marco;

    2015-01-01

    Three-phase DC-AC power converters suffer from power oscillation and overcurrent problems in case of unbalanced AC source voltage that can be caused by grid/generator faults. Existing solutions to handle these problems are properly selecting and controlling the positive and negative sequence...... converter can enable more flexible control targets, achieving better performances in the delivered power and load current when suffering from unbalanced AC voltage....

  7. Photometric amplitudes and phases of B-type main sequence pulsators: sources of inaccuracy

    CERN Document Server

    Szewczuk, Wojciech

    2010-01-01

    We discuss all possible sources of uncertainties in theoretical values of the photometric amplitudes and phases of B-type main sequence pulsators. These observables are of particular importance because they contain information about the mode geometry as well as about stellar physics. Here, we study effects of various parameters coming both from theory of linear nonadiabatic oscillations and from models of stellar atmospheres. In particular, we show effects of chemical composition, opacities and, for the first time, effects of the NLTE atmospheres.

  8. Analysis of Circularly Polarized Hemispheroidal Dielectric Resonator Antenna Phased Arrays Using the Method of Auxiliary Sources

    OpenAIRE

    Larsen, Niels Vesterdal; Breinbjerg, Olav

    2007-01-01

    The method of auxiliary sources is employed to model and analyze probe-fed hemispheroidal dielectric resonator antennas and arrays. Circularly polarized antenna elements of different designs are analyzed, and impedance bandwidths of up to 14.7% are achieved. Selected element designs are subsequently employed in a seven-element phased array. The array performance is analyzed with respect to scan loss and main beam directivity as a function of scan angle and frequency, and the influence of elem...

  9. Advanced Control Strategy for Single-Phase Voltage-Source Active Rectifier with Low Harmonic Emission

    Science.gov (United States)

    Blahník, Vojtĕch; Peroutka, Zdenĕk; Talla, Jakub

    2014-03-01

    This paper introduces the advanced control of single-phase voltage-source active rectifier. This control provide direct control of trolley-wire current and active damping of low-frequency disturbances at the converter ac side. Our proposed control strategy combines PR controller with feed-forward model and low-frequency harmonic compensator based on resonant controllers. Achieved experimental results show excellent converter behavior, where converter is fed by strongly distorted supply voltage.

  10. Injection of a Phase Modulated Source into the Z-Beamlet Laser for Increased Energy Extraction.

    Energy Technology Data Exchange (ETDEWEB)

    Rambo, Patrick K.; Armstrong, Darrell J.; Schwarz, Jens; Smith, Ian C; Shores, Jonathon; Speas, Christopher; Porter, John L.

    2014-11-01

    The Z-Beamlet laser has been operating at Sandia National Laboratories since 2001 to provide a source of laser-generated x-rays for radiography of events on the Z-Accelerator. Changes in desired operational scope have necessitated the increase in pulse duration and energy available from the laser system. This is enabled via the addition of a phase modulated seed laser as an alternative front-end. The practical aspects of deployment are discussed here.

  11. A plant-wide aqueous phase chemistry module describing pH variations and ion speciation/pairing in wastewater treatment process models.

    Science.gov (United States)

    Flores-Alsina, Xavier; Kazadi Mbamba, Christian; Solon, Kimberly; Vrecko, Darko; Tait, Stephan; Batstone, Damien J; Jeppsson, Ulf; Gernaey, Krist V

    2015-11-15

    There is a growing interest within the Wastewater Treatment Plant (WWTP) modelling community to correctly describe physico-chemical processes after many years of mainly focusing on biokinetics. Indeed, future modelling needs, such as a plant-wide phosphorus (P) description, require a major, but unavoidable, additional degree of complexity when representing cationic/anionic behaviour in Activated Sludge (AS)/Anaerobic Digestion (AD) systems. In this paper, a plant-wide aqueous phase chemistry module describing pH variations plus ion speciation/pairing is presented and interfaced with industry standard models. The module accounts for extensive consideration of non-ideality, including ion activities instead of molar concentrations and complex ion pairing. The general equilibria are formulated as a set of Differential Algebraic Equations (DAEs) instead of Ordinary Differential Equations (ODEs) in order to reduce the overall stiffness of the system, thereby enhancing simulation speed. Additionally, a multi-dimensional version of the Newton-Raphson algorithm is applied to handle the existing multiple algebraic inter-dependencies. The latter is reinforced with the Simulated Annealing method to increase the robustness of the solver making the system not so dependent of the initial conditions. Simulation results show pH predictions when describing Biological Nutrient Removal (BNR) by the activated sludge models (ASM) 1, 2d and 3 comparing the performance of a nitrogen removal (WWTP1) and a combined nitrogen and phosphorus removal (WWTP2) treatment plant configuration under different anaerobic/anoxic/aerobic conditions. The same framework is implemented in the Benchmark Simulation Model No. 2 (BSM2) version of the Anaerobic Digestion Model No. 1 (ADM1) (WWTP3) as well, predicting pH values at different cationic/anionic loads. In this way, the general applicability/flexibility of the proposed approach is demonstrated, by implementing the aqueous phase chemistry module in some

  12. Peptide-lanthanide cation equilibria in aqueous phase. I. Bound shifts for L-carnosine-praseodymium complexes

    Science.gov (United States)

    Mossoyan, J.; Asso, M.; Benlian, D.

    L-Carnosine complexes of Pr 3+ were characterized in aqueous solution by 1H NMR and potentiometric titration. A rigorous treatment of chemical shifts and pH variation data with lanthanide concentration is presented. Two different forms of the peptide ligand, forming simultaneously two complexes, were taken into account. At low pH values the cation is only coordinated at the carboxylate site of the ligand in a weak complex ( β2 = 6) whereas in neutral solution a stronger complex ( β1 = 37) is present as a consequence of the deprotonation of the imidazole ring. The computation of induced bound shifts † 2 and Δ1 for resonating nuclei of the peptide in both forms yields consistent figures. These provide the experimental basis for a conformational model which is usually not obtainable for labile complexes with low stability constants.

  13. Effects of source and receiver locations in predicting room transfer functions by a phased beam tracing method

    DEFF Research Database (Denmark)

    Jeong, Cheol-Ho; Ih, Jeong-Guon

    2012-01-01

    The accuracy of a phased beam tracing method in predicting transfer functions is investigated with a special focus on the positions of the source and receiver. Simulated transfer functions for various source-receiver pairs using the phased beam tracing method were compared with analytical Green’s...

  14. 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.

  15. A rapid and sensitive assay of perfluorocarboxylic acids in aqueous matrices by headspace solid phase microextraction-gas chromatography-triple quadrupole mass spectrometry.

    Science.gov (United States)

    Monteleone, Marcello; Naccarato, Attilio; Sindona, Giovanni; Tagarelli, Antonio

    2012-08-17

    The work aims at developing a rapid and sensitive method for the quantification of perfluorocarboxylic acids in aqueous matrices. The proposed analytical approach is based on the use of solid phase microextraction in headspace mode after a fast derivatization of the carboxylate function by propylchloroformate/propanol mixture. Several fibers were evaluated and the optimization of the parameters affecting the SPME process was carried out using a central composite design. The optimum working conditions in terms of response values were achieved by performing analysis with CAR/PDMS fiber at room temperature, without addition of NaCl, with a sample volume of 6 ml and an extraction time of 10 min. Assay of PFCAs was performed by using a gas chromatography-triple quadrupole mass spectrometry (GC-QqQ MS) system in negative chemical ionization mode with ammonia as reagent gas. An overall evaluation of all analytical parameters shows that the proposed method provides satisfactory results. In particular, the observed accuracies, ranging from 84.4% to 116.8%, and the RSD values in the range 0.4% and 14.5% confirm the effectiveness of the developed protocol in the assay of PFCAs content in aqueous matrices. Moreover, LOD and LOQ values ranging from 0.08 to 6.6 ng l(-1) and from 0.17 to 14.3 ng l(-1), respectively, can be considered very satisfactory. None of the compounds were detected in six samples of river collected in Calabria. PMID:22762954

  16. Modeling and Simulation of 3-Phase Voltage and Current Source Inverter using MATLAB/SIMULINK for Various Loads

    Directory of Open Access Journals (Sweden)

    Braj Kishor Verma

    2014-05-01

    Full Text Available In today’s world inverters are used to convert a single or multiple phase AC voltages from a DC supply source. Various types of inverters such as 1-phase inverters and 3-phase inverters are used for various industrial applications. Inverter comes in two categories which is voltage source inverter (VSI and current source inverter (CSI. In this paper work simulation of three phase VSI and CSI is performed using MATLAB/SIMULINK. THD is compared in voltage and current waveform and analyzed in different load conditions

  17. Comparison of two x-ray phase-contrast imaging methods with a microfocus source.

    Science.gov (United States)

    Zhou, T; Lundström, U; Thüring, T; Rutishauser, S; Larsson, D H; Stampanoni, M; David, C; Hertz, H M; Burvall, A

    2013-12-16

    We present a comparison for high-resolution imaging with a laboratory source between grating-based (GBI) and propagation-based (PBI) x-ray phase-contrast imaging. The comparison is done through simulations and experiments using a liquid-metal-jet x-ray microfocus source. Radiation doses required for detection in projection images are simulated as a function of the diameter of a cylindrical sample. Using monochromatic radiation, simulations show a lower dose requirement for PBI for small object features and a lower dose for GBI for larger object features. Using polychromatic radiation, such as that from a laboratory microfocus source, experiments and simulations show a lower dose requirement for PBI for a large range of feature sizes. Tested on a biological sample, GBI shows higher noise levels than PBI, but its advantage of quantitative refractive index reconstruction for multi-material samples becomes apparent. PMID:24514597

  18. Compact and stable temporally magnified tomography using a phase-locked broadband source.

    Science.gov (United States)

    Li, Bowen; Wei, Xiaoming; Tan, Sisi; Kang, Jiqiang; Wong, Kenneth K Y

    2016-04-01

    The temporally magnified tomography system is further improved in terms of resolution and imaging stability. We simplify the system configuration and improve the axial resolution simultaneously by utilizing a stabilized all-fiber broadband source. The highly stable spectrum of the source assisted by a phase-locked loop guarantees an improved imaging quality. In addition, the impact of the repetition-rate fluctuation of the source to the system stability is analyzed, which also applies to other temporal imaging systems. Achieving a 90-μm in-air resolution at 89-MHz A-scan rate and improved stability, we are taking one major step toward the practical application of this new optical tomographic modality. PMID:27192287

  19. FaCT Phase-I evaluation on the advanced aqueous reprocessing process (3). Highly effective dissolution technology for FBR MOX fuels

    International Nuclear Information System (INIS)

    Japan Atomic Energy Agency (JAEA) has been developing an efficient dissolution technology for irradiated MOX fuel in the framework of Fast Reactor Cycle Technology Development (FaCT) Project. In the fuel dissolution process for advanced aqueous reprocessing system named NEXT (New Extraction System for TRU Recovery), highly concentrated dissolution is required to adapt to the crystallization process. Optimum dissolution condition including short stroke shearing or pulverization of the irradiated fuel has been discussed, being based on the calculation results of continuous dissolver simulation code which reflects the results of dissolution tests using irradiated MOX fuel. We have been also developing rotary drum type continuous dissolver to adapt to the dissolution process for high heavy metal (U and Pu) concentration. This paper describes the summary and evaluation of R and D results on highly effective dissolution technology in the framework of FaCT Phase-I from 2006 to 2010. (author)

  20. Measurement of underground contamination of non-aqueous phase liquids (NAPLs) on the basis of the radon concentration in ground level air

    International Nuclear Information System (INIS)

    It was investigated whether measurements of radon concentrations in ground level air are a suitable method of detecting sub-surface soil contamination with non-aqueous phase liquids (NAPLs). The working postulation was that, due to the very high solubility of radon in NAPLs, and the resulting accumulation of radon in NAPLs, radon exhalation to the ground level air in the proximity of such NAPL contamination should be locally reduced, thus indicating contamination of sub-surface soils with NAPLs. The research work reported was to verify the working theory by way of experiments, and to finally develop a reliable detection method for NAPL contaminations. The investigations comprised theoretical studies, laboratory experiments, experiments in defined soil columns, and extensive field studies

  1. Synthesis and Evaluation of Molecularly Imprinted Polymeric Microspheres for Chloramphenicol by Aqueous Suspension Polymerization as a High Performance Liquid Chromatography Stationary Phase

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yan [Beijing Forestry Univ., Beijing (China); Lei, Jiandu [Univ., of Science and Technology, Beijing (Korea, Republic of)

    2013-06-15

    Molecularly imprinted microsphere for chloramphenicol (CAP) with high adsorption capacity and excellent selectivity is prepared by aqueous suspension polymerization, in which chloramphenicol is used as template molecule and ethyl acetate as porogen. The CAP-imprinted microspheres are used as high performance liquid chromatography (HPLC) stationary phase and packed into stainless steel column (150 mm Χ 4.6 mm i. d.) for selective separation of chloramphenicol. HPLC analysis suggests that chloramphenicol can be distinguished from not only its structural analogs but also other broad-spectrum antibiotic such as erythromycin and tetracycline. In addition, the binding experiments of CAP-imprinted microspheres are carried out in ethanol/water (1:4, V:V), the results indicate that the maximum apparent static binding capacity of molecularly imprinted microspheres is up to 66.64 mg g{sup -1} according to scatchard model.

  2. Isocratic non-aqueous reversed-phase high-performance liquid chromatographic separation of capsanthin and capsorubin in red peppers (Capsicum annuum L.), paprika and oleoresin.

    Science.gov (United States)

    Weissenberg, M; Schaeffler, I; Menagem, E; Barzilai, M; Levy, A

    1997-01-01

    A simple, rapid high-performance liquid chromatography method has been devised in order to separate and quantify the xanthophylls capsorubin and capasanthin present in red pepper (Capsicum annuum L.) fruits and preparations made from them (paprika and oleoresin). A reversed-phase isocratic non-aqueous system allows the separation of xanthophylls within a few minutes, with detection at 450 nm, using methyl red as internal standard to locate the various carotenoids and xanthophylls found in plant extracts. The selection of extraction solvents, mild saponification conditions, and chromatographic features is evaluated and discussed. The method is proposed for rapid screening of large plant populations, plant selection, as well as for paprika products and oleoresin, and also for nutrition and quality control studies.

  3. A plant wide aqueous phase chemistry model describing pH variations and ion speciation/pairing in wastewater treatment process models

    DEFF Research Database (Denmark)

    Flores-Alsina, X.; Mbamba, C. Kazadi; Solon, K.;

    There is a growing interest within the Wastewater Treatment Plant (WWTP) modelling community to correctly describe physico-chemical processes after many years of mainly focusing on biokinetics (Batstone et al., 2012). Indeed, future modelling needs, such as a plant-wide phosphorus (P) description...... presented and interfaced with industry standard models. The module involves extensive consideration of non-ideality by including ion activities instead of molar concentrations and complex ion pairing. The general equilibria are formulated as a set of Differential Algebraic Equations (DAEs) instead of...... cationic/anionic loads. In this way, the general applicability/flexibility of the proposed approach is demonstrated by implementing the aqueous phase chemistry module in some of the most frequently used WWTP process simulation models. Finally, it is shown how traditional wastewater modelling studies can be...

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

    Directory of Open Access Journals (Sweden)

    Y. B. Lim

    2015-06-01

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

  5. Improvement of oxygen-containing functional groups on olive stones activated carbon by ozone and nitric acid for heavy metals removal from aqueous phase.

    Science.gov (United States)

    Bohli, Thouraya; Ouederni, Abdelmottaleb

    2016-08-01

    Recently, modification of surface structure of activated carbons in order to improve their adsorption performance toward especial pollutants has gained great interest. Oxygen-containing functional groups have been devoted as the main responsible for heavy metal binding on the activated carbon surface; their introduction or enhancement needs specific modification and impregnation methods. In the present work, olive stones activated carbon (COSAC) undergoes surface modifications in gaseous phase using ozone (O3) and in liquid phase using nitric acid (HNO3). The activated carbon samples were characterized using N2 adsorption-desorption isotherm, SEM, pHpzc, FTIR, and Boehm titration. The activated carbon parent (COSAC) has a high surface area of 1194 m(2)/g and shows a predominantly microporous structure. Oxidation treatments with nitric acid and ozone show a decrease in both specific surface area and micropore volumes, whereas these acidic treatments have led to a fixation of high amount of surface oxygen functional groups, thus making the carbon surface more hydrophilic. Activated carbon samples were used as an adsorbent matrix for the removal of Co(II), Ni(II), and Cu(II) heavy metal ions from aqueous solutions. Adsorption isotherms were obtained at 30 °C, and the data are well fitted to the Redlich-Peterson and Langmuir equation. Results show that oxidized COSACs, especially COSAC(HNO3), are capable to remove more Co(II), Cu(II), and Ni(II) from aqueous solution. Nitric acid-oxidized olive stones activated carbon was tested in its ability to remove metal ions from binary systems and results show an important maximum adsorbed amount as compared to single systems.

  6. Aqueous phase hydrodeoxygenation of polyols over Pd/WO3-ZrO2: Role of Pd-WO3 interaction and hydrodeoxygenation pathway

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Changjun; Sun, Junming; Brown, Heather M.; Marin-Flores, Oscar G.; Bays, J. Timothy; Karim, Ayman M.; Wang, Yong

    2016-07-01

    Aqueous-phase hydrodeoxygenation of sugar and sugar-derived molecules can be used to produce a range of alkanes and oxygenates. In this paper, we have identified the reaction intermediates and reaction chemistry for the aqueous-phase hydrodeoxygenation of sorbitol over a bifunctional catalyst (Pt/SiO2–Al2O3) that contains both metal (Pt) and acid (SiO2–Al2O3) sites. A wide variety of reactions occur in this process including Csingle bondC bond cleavage, Csingle bondO bond cleavage, and hydrogenation reactions. The key Csingle bondC bond cleavage reactions include: retro-aldol condensation and decarbonylation, which both occur on metal catalytic sites. Dehydration is the key Csingle bondO bond cleavage reaction and occurs on acid catalytic sites. Sorbitol initially undergoes dehydration and ring closure to produce cyclic C6 molecules or retro-aldol condensation reactions to produce primarily C3 polyols. Isosorbide is the major final product from sorbitol dehydration. Isosorbide then undergoes ring opening hydrogenation reactions and a dehydration/hydrogenation step to form 1,2,6-hexanetriol. The hexanetriol is then converted into hexanol and hexane by dehydration/hydrogenation. Smaller oxygenates are produced by Csingle bondC bond cleavage. These smaller oxygenates undergo dehydration/hydrogenation reactions to produce alkanes from C1–C5. The results from this paper suggest that hydrodeoxygenation chemistry can be tuned to make a wide variety of products from biomass-derived oxygenates.

  7. Use of a Combined Technology of Ultrasonication, Three-Phase Partitioning, and Aqueous Enzymatic Oil Extraction for the Extraction of Oil from Spirogyra sp.

    Directory of Open Access Journals (Sweden)

    Adisheshu Reddy

    2014-01-01

    Full Text Available Algal oil from Spirogyra sp. was extracted using a combined technology of ultrasonication, three-phase partitioning, and aqueous enzymatic oil extraction. Ultrasonication was done to rupture the cell wall and papain was used for an easier release of the trapped oil. The salt concentration for three-phase partitioning, preincubation period with (or without the protease, and its operational temperature were optimized for a maximum possible yield of the oil and the effect of ultrasonication, and three-phase partitioning with (or without the protease were studied. It was found that under optimized conditions at 50% ammonium sulphate concentration using tert-butanol (in 1 : 1, v/v ratio a presonicated and papain treated algal suspension could produce 24% (w/w, dry weight oil within few hours which was ten times higher as compared to the oil obtained by Soxhlet extraction using hexane and two times higher than the oil obtained without using the protease.

  8. 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

  9. Effect of the water content on the retention and enantioselectivity of albendazole and fenbendazole sulfoxides using amylose-based chiral stationary phases in organic-aqueous conditions.

    Science.gov (United States)

    Materazzo, Sabrina; Carradori, Simone; Ferretti, Rosella; Gallinella, Bruno; Secci, Daniela; Cirilli, Roberto

    2014-01-31

    Four commercially available immobilized amylose-derived CSPs (Chiralpak IA-3, Chiralpak ID-3, Chiralpak IE-3 and Chiralpak IF-3) were used in the HPLC analysis of the chiral sulfoxides albendazole (ABZ-SO) and fenbendazole (FBZ-SO) and their in vivo sulfide precursor (ABZ and FBZ) and sulfone metabolite (ABZ-SO2 and FBZ-SO2) under organic-aqueous mode. U-shape retention maps, established by varying the water content in the acetonitrile- and ethanol-water mobile phases, were indicative of two retention mechanisms operating on the same CSP. The dual retention behavior of polysaccharide-based CSPs was exploited to design greener enantioselective and chemoselective separations in a short time frame. The enantiomers of ABZ-SO and FBZ-SO were baseline resolved with water-rich mobile phases (with the main component usually being 50-65% water in acetonitrile) on the IF-3 CSP and ethanol-water 100:5 mixture on the IA-3 and IE-3 CSPs. A simultaneous separation of ABZ (or FBZ), enantiomers of the corresponding sulfoxide and sulfone was achieved on the IA-3 using ethanol-water 100:60 (acetonitrile-water 100:100 for FBZ) as a mobile phase.

  10. Aqueous two-phase system cold-set gelation using natural and recombinant probiotic lactic acid bacteria as a gelling agent.

    Science.gov (United States)

    Léonard, Lucie; Husson, Florence; Langella, Philippe; Châtel, Jean-Marc; Saurel, Rémi

    2016-05-01

    The present study aimed to entrap probiotic lactic acid bacteria (LAB) in a sodium alginate and sodium caseinate aqueous two-phase gel system. The natural acidifying properties of two therapeutic probiotic LAB were exploited to liberate calcium ions progressively from calcium carbonate (CaCO3), which caused the gelation of the co-existing phases. Bi-biopolymeric matrix gelation of GDL/CaCO3 or LAB/CaCO3 was monitored by dynamic rheological measurements, and the final gels were characterized by frequency dependence measurements and confocal laser scanning microscopy. Weak to strong gels were formed with an elastic modulus G' from 10 to 1.000Pa, respectively. After cold-set gelation of our system, confocal laser scanning microscopy showed spherical protein microdomains trapped within a calcium alginate network. LAB cells were stained to study their partition in the self-gelling matrices. Our LAB strains showed two different behaviors, which may relate to the exopolysaccharide production: (i) Lactobacillus plantarum CNRZ1997 cells were found mainly in continuous alginate networks, whereas (ii) Lactococcus lactis cells were localized in protein microdomains. This alginate-caseinate phase-separated system that was self-gelled by LAB cells may be an innovative approach for immobilizing and protecting LAB cells. PMID:26874119

  11. A quantitative PGNAA study for use in aqueous solution measurements using Am-Be neutron source and BGO scintillation detector

    Science.gov (United States)

    Ghal-Eh, N.; Ahmadi, P.; Doost-Mohammadi, V.

    2016-02-01

    A prompt gamma neutron activation analysis (PGNAA) system including an Am-Be neutron source and BGO scintillation detector are used for quantitative analysis of bulk samples. Both Monte Carlo-simulated and experimental data are considered as input data libraries for two different procedures based on neural network and least squares methods. The results confirm the feasibility and precision of the proposed methods.

  12. Aqueous phase preparation of ultrasmall MoSe2 nanodots for efficient photothermal therapy of cancer cells

    Science.gov (United States)

    Yuwen, Lihui; Zhou, Jiajia; Zhang, Yuqian; Zhang, Qi; Shan, Jingyang; Luo, Zhimin; Weng, Lixing; Teng, Zhaogang; Wang, Lianhui

    2016-01-01

    Photothermal therapy (PTT) is a promising cancer treatment with both high effectiveness and fewer side effects. However, an ideal PTT agent not only needs strong absorption of near-infrared (NIR) light and high photothermal conversion efficiency, but also needs good biocompatibility, stability, and small size, which makes the design and preparation of a novel PTT agent a great challenge. In this work, we developed an ultrasonication-assisted liquid exfoliation method for the direct preparation of ultrasmall (2-3 nm) MoSe2 nanodots (NDs) in aqueous solution and demonstrated their superior properties as a PTT agent. The as-prepared MoSe2 NDs have strong absorption of NIR light and high photothermal conversion efficiency of about 46.5%. In vitro cellular experiments demonstrate that MoSe2 NDs have negligible cytotoxicity and can efficiently kill HeLa cells (human cervical cell line) under NIR laser (785 nm) irradiation.Photothermal therapy (PTT) is a promising cancer treatment with both high effectiveness and fewer side effects. However, an ideal PTT agent not only needs strong absorption of near-infrared (NIR) light and high photothermal conversion efficiency, but also needs good biocompatibility, stability, and small size, which makes the design and preparation of a novel PTT agent a great challenge. In this work, we developed an ultrasonication-assisted liquid exfoliation method for the direct preparation of ultrasmall (2-3 nm) MoSe2 nanodots (NDs) in aqueous solution and demonstrated their superior properties as a PTT agent. The as-prepared MoSe2 NDs have strong absorption of NIR light and high photothermal conversion efficiency of about 46.5%. In vitro cellular experiments demonstrate that MoSe2 NDs have negligible cytotoxicity and can efficiently kill HeLa cells (human cervical cell line) under NIR laser (785 nm) irradiation. Electronic supplementary information (ESI) available: Characterization, size distribution and EDS spectrum of MoSe2 NDs, calculation of

  13. Acute phase IL-10 plasma concentration associates with the high risk sources of cardiogenic stroke.

    Directory of Open Access Journals (Sweden)

    Otso Arponen

    Full Text Available Etiological assessment of stroke is essential for accurate treatment decisions and for secondary prevention of recurrence. There is evidence that interleukin-10 (IL-10 associates with ischemic stroke. The aim of this prospective study was to assess the levels of IL-10 in ischemic stroke with unknown or suspected cardiogenic etiology, and evaluate the correlation between IL-10 plasma concentration and the number of diagnosed high risk sources for cardioembolism.A total of 141 patients (97 males; mean age 61±11 years with acute ischemic stroke with unknown etiology or suspected cardiogenic etiology other than known atrial fibrillation (AF underwent imaging investigations to assess high risk sources for cardioembolic stroke established by the European Association of Echocardiography (EAE. IL-10 was measured on admission to the hospital and on a three month follow-up visit.Acute phase IL-10 concentration was higher in patients with EAE high risk sources, and correlated with their number (p<0.01. In patients with no risk sources (n = 104, the mean IL-10 concentration was 2.7±3.1 ng/L (range 0.3-16.3 ng/L, with one risk source (n = 26 3.7±5.5 ng/L (0.3-23.6 ng/L, with two risk sources (n = 10 7.0±10.0 ng/L (1.29-34.8 ng/L and with three risk sources (n = 1 37.2 ng/L. IL-10 level was not significantly associated with cerebral infarct volume, presence of previous or recent myocardial infarction, carotid/vertebral artery atherosclerosis, paroxysmal AF registered on 24-hour ECG Holter monitoring or given intravenous thrombolytic treatment.IL-10 plasma concentration correlates independently with the number of EAE cardioembolic risk sources in patients with acute stroke. IL-10 may have potential to improve differential diagnostics of stroke with unknown etiology.

  14. Reconstructing source-sink dynamics in a population with a pelagic dispersal phase.

    Directory of Open Access Journals (Sweden)

    Kun Chen

    Full Text Available For many organisms, the reconstruction of source-sink dynamics is hampered by limited knowledge of the spatial assemblage of either the source or sink components or lack of information on the strength of the linkage for any source-sink pair. In the case of marine species with a pelagic dispersal phase, these problems may be mitigated through the use of particle drift simulations based on an ocean circulation model. However, when simulated particle trajectories do not intersect sampling sites, the corroboration of model drift simulations with field data is hampered. Here, we apply a new statistical approach for reconstructing source-sink dynamics that overcomes the aforementioned problems. Our research is motivated by the need for understanding observed changes in jellyfish distributions in the eastern Bering Sea since 1990. By contrasting the source-sink dynamics reconstructed with data from the pre-1990 period with that from the post-1990 period, it appears that changes in jellyfish distribution resulted from the combined effects of higher jellyfish productivity and longer dispersal of jellyfish resulting from a shift in the ocean circulation starting in 1991. A sensitivity analysis suggests that the source-sink reconstruction is robust to typical systematic and random errors in the ocean circulation model driving the particle drift simulations. The jellyfish analysis illustrates that new insights can be gained by studying structural changes in source-sink dynamics. The proposed approach is applicable for the spatial source-sink reconstruction of other species and even abiotic processes, such as sediment transport.

  15. Neutrophils are essential as a source of IL-17 in the effector phase of arthritis.

    Directory of Open Access Journals (Sweden)

    Masaki Katayama

    Full Text Available OBJECTIVE: Th17 has been shown to have a pivotal role in the development of arthritis. However, the role of IL-17 in the T cell-independent effector phase has not fully been examined. We investigated whether IL-17 is involved in the effector phase of arthritis by using K/BxN serum-induced arthritis model. METHODS: K/BxN serum was transferred into IL-17 knockout (KO mice, SCID mice and their control mice, and arthritis was evaluated over time. In order to clarify the source of IL-17 in the effector phase, neutrophils or CD4+ T cells collected from IL-17 KO or control mice were injected into IL-17 KO recipient mice together with K/BxN serum. To examine if neutrophils secrete IL-17 upon stimulation, neutrophils were stimulated with immune complex in vitro and IL-17 in the supernatant was measured by ELISA. RESULTS: K/BxN serum-induced arthritis was much less severe in IL-17 KO mice than in WT mice. Since K/BxN serum-transferred SCID mice developed severe arthritis with high serum IL-17 concentration, we speculated neutrophils are the responsible player as an IL-17 source. When wild type (WT but not IL-17 KO neutrophils were co-injected with K/BxN serum into IL-17 KO mice, arthritis was exacerbated, whereas co-injection of WT CD4+ T cells had no effect. In vitro, stimulation of neutrophils with immune complex caused IL-17 secretion. CONCLUSIONS: Neutrophils are essential as a source of IL-17 in the effector phase of arthritis. The trigger of secreting IL-17 from neutrophils may be immune complex.

  16. Cell separation by immunoaffinity partitioning with polyethylene glycol-modified Protein A in aqueous polymer two-phase systems

    Science.gov (United States)

    Karr, Laurel J.; Van Alstine, James M.; Snyder, Robert S.; Shafer, Steven G.; Harris, J. Milton

    1988-01-01

    Previous work has shown that polyethylene glycol (PEG)-bound antibodies can be used as affinity ligands in PEG-dextran two-phase systems to provide selective partitioning of cells to the PEG-rich phase. In the present work it is shown that immunoaffinity partitioning can be simplified by use of PEG-modified Protein A which complexes with unmodified antibody and cells and shifts their partitioning into the PEG-rich phase, thus eliminating the need to prepare a PEG-modified antibody for each cell type. In addition, the paper provides a more rigorous test of the original technique with PEG-bound antibodies by showing that it is effective at shifting the partitioning of either cell type of a mixture of two cell populations.

  17. Optimization of the Parameters Affecting the Fenton Process for Decolorization of Reactive Red 198 (RR-198 from the Aqueous Phase

    Directory of Open Access Journals (Sweden)

    Mansooreh Dehghani

    2015-10-01

    Full Text Available Background: Recently, there has been a great concern about the consumption of dyes because of their toxicity, mutagenicity, carcinogenicity, and persistence in the aquatic environment. Reactive dyes are widely used in textile industry. Advanced oxidation processes are one of the cost-effective methods for the removal of these dyes. The main aims of this study were determining the feasibility of using Fenton process in removing Reactive Red 198 (RR-198 dye from aqueous solution and determining the optimal conditions. Methods: This is a cross-sectional study conducted at a laboratory scale. A total of 69 samples were considered and the effect of pH, Fe (II concentration, H2O2 concentration, initial dye concentration and reaction time were investigated. Results: According to the results, a maximum removal efficiency of 92% was obtained at pH of 3 and the reaction time of 90 min; also, the concentration of Fe (II, H2O2, initial dye concentration were 100 mg/L, 50 mg/L, and 100 mg/L, respectively. The results revealed that by increasing the concentration of Fe (II, H2O2 and initial dye, the removal efficiency was increased. Conclusions: The results showed that Fenton process could be used as a cost-effective method for removing RR-198 dye from textile wastewater efficiently.

  18. Laser-driven phase transitions in aqueous colloidal gold nanoparticles under high pressure: picosecond pump-probe study.

    Science.gov (United States)

    Hashimoto, Shuichi; Katayama, Tetsuro; Setoura, Kenji; Strasser, Michael; Uwada, Takayuki; Miyasaka, Hiroshi

    2016-02-14

    Pump-probe transient extinction spectroscopy was used to analyze 355 nm picosecond laser heating-induced phenomena in 60 nm-diameter aqueous gold nanoparticles (AuNPs) under a high pressure of 60 MPa. Kinetic spectroscopy revealed that a supercritical layer surrounding the AuNP nucleated with a lifetime of approximately 1 ns during its dynamic expansion and decay for a fluence of 19.6 mJ cm(-2). Moreover, in the post-mortem transmission electron micrographs we observed a number of fragments, a small percentage of size-reduced cores, and erupted particles among the intact particles after 60 shots, suggesting that evaporation occurred under laser illumination. The particle temperature calculation indicated that evaporation begins with a liquid droplet AuNP surrounded by a supercritical layer at temperatures below the boiling point of gold. By applying high pressure, we obtained a clear picture of the evaporation event, which was not possible at ambient pressure because bubble formation caused particle temperatures to rise uncontrollably. In this study, we shed light on the critical role of the supercritical layer formed around the AuNP under high pressure during laser-induced evaporation. PMID:26812175

  19. Room-Temperature and Aqueous-Phase Synthesis of Plasmonic Molybdenum Oxide Nanoparticles for Visible-Light-Enhanced Hydrogen Generation.

    Science.gov (United States)

    Shi, Jiayuan; Kuwahara, Yasutaka; Wen, Meicheng; Navlani-García, Miriam; Mori, Kohsuke; An, Taicheng; Yamashita, Hiromi

    2016-09-01

    A straightforward aqueous synthesis of MoO3-x nanoparticles at room temperature was developed by using (NH4 )6 Mo7 O24 ⋅4 H2 O and MoCl5 as precursors in the absence of reductants, inert gas, and organic solvents. SEM and TEM images indicate the as-prepared products are nanoparticles with diameters of 90-180 nm. The diffuse reflectance UV-visible-near-IR spectra of the samples indicate localized surface plasmon resonance (LSPR) properties generated by the introduction of oxygen vacancies. Owing to its strong plasmonic absorption in the visible-light and near-infrared region, such nanostructures exhibit an enhancement of activity toward visible-light catalytic hydrogen generation. MoO3-x nanoparticles synthesized with a molar ratio of Mo(VI) /Mo(V) 1:1 show the highest yield of H2 evolution. The cycling catalytic performance has been investigated to indicate the structural and chemical stability of the as-prepared plasmonic MoO3-x nanoparticles, which reveals its potential application in visible-light catalytic hydrogen production. PMID:27555123

  20. Aqueous phase adsorption of cephalexin by walnut shell-based activated carbon: A fixed-bed column study

    Science.gov (United States)

    Nazari, Ghadir; Abolghasemi, Hossein; Esmaieli, Mohamad; Sadeghi Pouya, Ehsan

    2016-07-01

    The walnut shell was used as a low cost adsorbent to produce activated carbon (AC) for the removal of cephalexin (CFX) from aqueous solution. A fixed-bed column adsorption was carried out using the walnut shell AC. The effect of various parameters like bed height (1.5, 2 and 2.5 cm), flow rate (4.5, 6 and 7.5 mL/min) and initial CFX concentration (50, 100 and 150 mg/L) on the breakthrough characteristics of the adsorption system was investigated at optimum pH 6.5. The highest bed capacity of 211.78 mg/g was obtained using 100 mg/L inlet drug concentration, 2 cm bed height and 4.5 mL/min flow rate. Three kinetic models, namely Adam's-Bohart, Thomas and Yoon-Nelson were applied for analysis of experimental data. The Thomas and Yoon-Nelson models were appropriate for walnut shell AC column design under various conditions. The experimental adsorption capacity values were fitted to the Bangham and intra-particle diffusion models in order to propose adsorption mechanisms. The effect of temperature on the degradation of CFX was also studied.

  1. Results of an aqueous source term model for a radiological risk assessment of the Drigg LLW Site, U.K.

    OpenAIRE

    Small, J. S.; Humphreys, P. N.; Johnstone, T. L.; Plant, R.; Randall, M. G.; Trivedi, D. P.

    1999-01-01

    A radionuclide source term model has been developed which simulates the biogeochemical evolution of the Drigg low level waste (LLW) disposal site. The DRINK (DRIgg Near field Kinetic) model provides data regarding radionuclide concentrations in groundwater over a period of 100,000 years, which are used as input to assessment calculations for a groundwater pathway. The DRINK model also provides input to human intrusion and gaseous assessment calculations through simulation of the solid radionu...

  2. Results of an aqueous source term model for a radiological risk assessment of the Drigg LLW site

    OpenAIRE

    Small, J.; Humphreys, Paul; Johnstone, T. J.; Plant, R.; Randall, M. G.; Trivedi, D. P.

    2000-01-01

    A radionuclide source term model has been developed which simulates the biogeochemical evolution of the Drigg low level waste (LLW) disposal site. The DRINK (DRIgg Near field Kinetic) model provides data regarding radionuclide concentrations in groundwater over a period of 100,000 years, which are used as inputs to safety assessment calculations. The DRINK model considers the coupled interaction of the effects of fluid flow, microbiology, corrosion, chemical reaction, sorption and radioactive...

  3. Radio over fiber transceiver employing phase modulation of an optical broadband source.

    Science.gov (United States)

    Grassi, Fulvio; Mora, José; Ortega, Beatriz; Capmany, José

    2010-10-11

    This paper proposes a low-cost RoF transceiver for multichannel SCM/WDM signal distribution suitable for future broadband access networks. The transceiver is based on the phase modulation of an optical broadband source centered at third transmission window. Prior to phase modulation the optical broadband source output signal is launched into a Mach-Zehnder interferometer structure, as key device enabling radio signals propagation over the optical link. Furthermore, an optical CWDM is employed to create a multichannel scenario by performing the spectral slicing of the modulated optical signal into a number of channels each one conveying the information from the central office to different base stations. The operation range is up to 20 GHz with a modulation bandwidth around of 500 MHz. Experimental results of the transmission of SCM QPSK and 64-QAM data through 20 Km of SMF exhibit good EVM results in the operative range determined by the phase-to-intensity conversion process. The proposed approach shows a great suitability for WDM networks based on RoF signal transport and also represents a cost-effective solution for passive optical networks. PMID:20941075

  4. Low-dose phase contrast tomography with conventional x-ray sources

    Energy Technology Data Exchange (ETDEWEB)

    Hagen, C. K., E-mail: charlotte.hagen.10@ucl.ac.uk; Endrizzi, M.; Diemoz, P. C.; Olivo, A. [Department of Medical Physics and Bioengineering, University College London, Malet Place, Gower Street, London WC1E 6BT (United Kingdom); Munro, P. R. T. [Optical + Biomedical Engineering Laboratory, School of Electrical, Electronic and Computer Engineering, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia and Centre for Microscopy, Characterisation, and Analysis, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009 (Australia)

    2014-07-15

    Purpose: The edge illumination (EI) x-ray phase contrast imaging (XPCi) method has been recently further developed to perform tomographic and, thus, volumetric imaging. In this paper, the first tomographic EI XPCi images acquired with a conventional x-ray source at dose levels below that used for preclinical small animal imaging are presented. Methods: Two test objects, a biological sample and a custom-built phantom, were imaged with a laboratory-based EI XPCi setup in tomography mode. Tomographic maps that show the phase shift and attenuating properties of the object were reconstructed, and analyzed in terms of signal-to-noise ratio and quantitative accuracy. Dose measurements using thermoluminescence devices were performed. Results: The obtained images demonstrate that phase based imaging methods can provide superior results compared to attenuation based modalities for weakly attenuating samples also in 3D. Moreover, and, most importantly, they demonstrate the feasibility of low-dose imaging. In addition, the experimental results can be considered quantitative within the constraints imposed by polychromaticity. Conclusions: The results, together with the method's dose efficiency and compatibility with conventional x-ray sources, indicate that tomographic EI XPCi can become an important tool for the routine imaging of biomedical samples.

  5. Phased Array Noise Source Localization Measurements Made on a Williams International FJ44 Engine

    Science.gov (United States)

    Podboy, Gary G.; Horvath, Csaba

    2010-01-01

    A 48-microphone planar phased array system was used to acquire noise source localization data on a full-scale Williams International FJ44 turbofan engine. Data were acquired with the array at three different locations relative to the engine, two on the side and one in front of the engine. At the two side locations the planar microphone array was parallel to the engine centerline; at the front location the array was perpendicular to the engine centerline. At each of the three locations, data were acquired at eleven different engine operating conditions ranging from engine idle to maximum (take off) speed. Data obtained with the array off to the side of the engine were spatially filtered to separate the inlet and nozzle noise. Tones occurring in the inlet and nozzle spectra were traced to the low and high speed spools within the engine. The phased array data indicate that the Inflow Control Device (ICD) used during this test was not acoustically transparent; instead, some of the noise emanating from the inlet reflected off of the inlet lip of the ICD. This reflection is a source of error for far field noise measurements made during the test. The data also indicate that a total temperature rake in the inlet of the engine is a source of fan noise.

  6. Development of a gas phase source for perfluoroalkyl acids to examine atmospheric sampling methods.

    Science.gov (United States)

    MacInnis, John J; VandenBoer, Trevor C; Young, Cora J

    2016-06-21

    An inability to produce environmentally relevant gaseous mixing ratios of perfluoroalkyl acids (PFAAs), ubiquitous global contaminants, limits the analytical reliability of atmospheric chemists to make accurate gas and particulate measurements that are demonstrably free of interferences due to sampling artefacts. A gas phase source for PFAAs based on the acid displacement mechanism using perfluoropropionate (PFPrA), perfluorobutanoate (PFBA), perfluorohexanoate (PFHxA), and perfluorooctanoate (PFOA) has been constructed. The displacement efficiency of gas phase perfluorocarboxylic acids (PFCAs) is inversely related to chain length. Decreasing displacement efficiencies for PFPrA, PFBA, PFHxA, and PFOA were 90% ± 20%, 40% ± 10%, 40% ± 10%, 9% ± 4%, respectively. Generating detectable amounts of gas phase perfluorosulfonic acids (PFSAs) was not possible. It is likely that lower vapour pressure and much higher acidity play a role in this lack of emission. PFCA emission rates were not elevated by increasing relative humidity (25%-75%), nor flow rate of carrier gas from 33-111 sccm. Overall, reproducible gaseous production of PFCAs was within the error of the production of hydrochloric acid (HCl) as a displacing acid (±20%) and was accomplished using a dry nitrogen flow of 33 ± 2 sccm. A reproducible mass emission rate of 0.97 ± 0.10 ng min(-1) (n = 8) was observed for PFBA. This is equivalent to an atmospheric mixing ratio of 12 ppmv, which is easily diluted to environmentally relevant mixing ratios of PFBA. Conversely, generating gas phase perfluorononanoic acid (PFNA) by sublimating the solid acid under the same conditions produced a mass emission rate of 2800 ng min(-1), which is equivalent to a mixing ratio of 18 ppthv and over a million times higher than suspected atmospheric levels. Thus, for analytical certification of atmospheric sampling methods, generating gas phase standards for PFCAs is best accomplished using acid displacement under dry conditions

  7. Analysis of Discontinuous Space Vector PWM Techniques for a Seven-Phase Voltage Source Inverter

    Directory of Open Access Journals (Sweden)

    Mohd. Arif Khan

    2012-03-01

    Full Text Available This paper presents discontinuous space vector PWM (DPWM techniques for a seven-phase voltage source inverter (VSI. Space vector model of a seven-phase VSI shows that there exist 128 space vectors with different lengths and maps into fourteen sided polygons. A number of possibilities could arise to implement modulation of inverter legs due to large number of available space voltage vectors. Two strategies are adopted here; one utilising large and two middle sets of space vectors to implement discontinuous space vector PWM. Clamping of legs of inverter to either positive or negative dc bus leads to discontinuity in the switching and consequently offers reduced switching loss modulation strategy. A significant reduction in switching losses can be achieved while employing DPWM in a seven-phase VSI. A generalised method is also proposed to realize the DPWM in a seven-phase VSI. Comparison of continuous and discontinuous PWM is presented in terms of switching current ripple. The experimental set-up is illustrated and the experimental results are presented.

  8. Achromatic approach to phase-based multi-modal imaging with conventional X-ray sources.

    Science.gov (United States)

    Endrizzi, Marco; Vittoria, Fabio A; Kallon, Gibril; Basta, Dario; Diemoz, Paul C; Vincenzi, Alessandro; Delogu, Pasquale; Bellazzini, Ronaldo; Olivo, Alessandro

    2015-06-15

    Compatibility with polychromatic radiation is an important requirement for an imaging system using conventional rotating anode X-ray sources. With a commercially available energy-resolving single-photon-counting detector we investigated how broadband radiation affects the performance of a multi-modal edge-illumination phase-contrast imaging system. The effect of X-ray energy on phase retrieval is presented, and the achromaticity of the method is experimentally demonstrated. Comparison with simulated measurements integrating over the energy spectrum shows that there is no significant loss of image quality due to the use of polychromatic radiation. This means that, to a good approximation, the imaging system exploits radiation in the same way at all energies typically used in hard-X-ray imaging. PMID:26193618

  9. Synthesis of single phase magnetite, Fe3O4 nanocrystallites using single source precursor

    Science.gov (United States)

    Disale, Sujit D.; Garje, Shivram S.

    2010-10-01

    Nanocrystalline Fe3O4 have been prepared using Fe(benzsczH)2Cl2 (where, benzsczH = benzaldehyde semicarbazone) as a single-source precursor. Fe(benzsczH)2Cl2 was characterized by elemental analyses, molar conductivity measearments, magnetic susceptibility studies, cyclic voltammetry and IR spectroscopy. The pyrolysis and solvothermal decomposition in ethylene glycol of this complex resulted in cubic phase Fe3O4 nanocrystals. These nanocrystals were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive analysis by X-rays, IR spectroscopy and hysteresis loop. XRD shows formation of cubic phase Fe3O4 for nanocrystallites obtained by both the methods. The TEM of nanoparticles obtained by pyrolysis show cubic shape plate-like morphology with average grain size of 54 nm and the nanoparticles obtained from solvothermal decomposition route have spherical shape morphology with average grain size of 16 nm.

  10. Propagation-based phase-contrast tomography for high-resolution lung imaging with laboratory sources

    Science.gov (United States)

    Krenkel, Martin; Töpperwien, Mareike; Dullin, Christian; Alves, Frauke; Salditt, Tim

    2016-03-01

    We have performed high-resolution phase-contrast tomography on whole mice with a laboratory setup. Enabled by a high-brilliance liquid-metal-jet source, we show the feasibility of propagation-based phase contrast in local tomography even in the presence of strongly absorbing surrounding tissue as it is the case in small animal imaging of the lung. We demonstrate the technique by reconstructions of the mouse lung for two different fields of view, covering the whole organ, and a zoom to the local finer structure of terminal airways and alveoli. With a resolution of a few micrometers and the wide availability of the technique, studies of larger biological samples at the cellular level become possible.

  11. Propagation-based phase-contrast tomography for high-resolution lung imaging with laboratory sources

    Directory of Open Access Journals (Sweden)

    Martin Krenkel

    2016-03-01

    Full Text Available We have performed high-resolution phase-contrast tomography on whole mice with a laboratory setup. Enabled by a high-brilliance liquid-metal-jet source, we show the feasibility of propagation-based phase contrast in local tomography even in the presence of strongly absorbing surrounding tissue as it is the case in small animal imaging of the lung. We demonstrate the technique by reconstructions of the mouse lung for two different fields of view, covering the whole organ, and a zoom to the local finer structure of terminal airways and alveoli. With a resolution of a few micrometers and the wide availability of the technique, studies of larger biological samples at the cellular level become possible.

  12. Phase 1 environmental report for the Advanced Neutron Source at Oak Ridge National Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Blasing, T.J.; Brown, R.A.; Cada, G.F.; Easterly, C.; Feldman, D.L.; Hagan, C.W.; Harrington, R.M.; Johnson, R.O.; Ketelle, R.H.; Kroodsma, R.L.; McCold, L.N.; Reich, W.J.; Scofield, P.A.; Socolof, M.L.; Taleyarkhan, R.P.; Van Dyke, J.W.

    1992-02-01

    The US Department of Energy (DOE) has proposed the construction and operation of the Advanced Neutron Source (ANS), a 330-MW(f) reactor, at Oak Ridge National Laboratory (ORNL) to support neutron scattering and nuclear physics experiments. ANS would provide a steady-state source of neutrons that are thermalized to produce sources of hot, cold, and very coal neutrons. The use of these neutrons in ANS experiment facilities would be an essential component of national research efforts in basic materials science. Additionally, ANS capabilities would include production of transplutonium isotopes, irradiation of potential fusion and fission reactor materials, activation analysis, and production of medical and industrial isotopes such as {sup 252}Cf. Although ANS would not require licensing by the US Nuclear Regulatory Commission (NRC), DOE regards the design, construction, and operation of ANS as activities that would produce a licensable facility; that is, DOE is following the regulatory guidelines that NRC would apply if NRC were licensing the facility. Those guidelines include instructions for the preparation of an environmental report (ER), a compilation of available data and preliminary analyses regarding the environmental impacts of nuclear facility construction and operation. The ER, described and outlined in NRC Regulatory Guide 4.2, serves as a background document to facilitate the preparation of environmental impact statements (EISs). Using Regulatory Guide 4.2 as a model, this ANS ER provides analyses and information specific to the ANS site and area that can be adopted (and modified, if necessary) for the ANS EIS. The ER is being prepared in two phases. Phase 1 ER includes many of the data and analyses needed to prepare the EIS but does not include data or analyses of alternate sites or alternate technologies. Phase 2 ER will include the additional data and analyses stipulated by Regulatory Guide 4.2.

  13. Phase 1 environmental report for the Advanced Neutron Source at Oak Ridge National Laboratory

    International Nuclear Information System (INIS)

    The US Department of Energy (DOE) has proposed the construction and operation of the Advanced Neutron Source (ANS), a 330-MW(f) reactor, at Oak Ridge National Laboratory (ORNL) to support neutron scattering and nuclear physics experiments. ANS would provide a steady-state source of neutrons that are thermalized to produce sources of hot, cold, and very coal neutrons. The use of these neutrons in ANS experiment facilities would be an essential component of national research efforts in basic materials science. Additionally, ANS capabilities would include production of transplutonium isotopes, irradiation of potential fusion and fission reactor materials, activation analysis, and production of medical and industrial isotopes such as 252Cf. Although ANS would not require licensing by the US Nuclear Regulatory Commission (NRC), DOE regards the design, construction, and operation of ANS as activities that would produce a licensable facility; that is, DOE is following the regulatory guidelines that NRC would apply if NRC were licensing the facility. Those guidelines include instructions for the preparation of an environmental report (ER), a compilation of available data and preliminary analyses regarding the environmental impacts of nuclear facility construction and operation. The ER, described and outlined in NRC Regulatory Guide 4.2, serves as a background document to facilitate the preparation of environmental impact statements (EISs). Using Regulatory Guide 4.2 as a model, this ANS ER provides analyses and information specific to the ANS site and area that can be adopted (and modified, if necessary) for the ANS EIS. The ER is being prepared in two phases. Phase 1 ER includes many of the data and analyses needed to prepare the EIS but does not include data or analyses of alternate sites or alternate technologies. Phase 2 ER will include the additional data and analyses stipulated by Regulatory Guide 4.2

  14. EFFECT OF ALCOHOL ON AQUEOUS TWO-PHASE SYSTEM PROPERTIES OF SDS/CTAB/H2O/Na2SO4 SYSTEM%醇对正负离子表面活性剂双水相性质的影响

    Institute of Scientific and Technical Information of China (English)

    滕弘霓; 王利

    2004-01-01

    The effect of alcohol on the aqueous two-phase system properties of SDS/CTAB/H2O/Na2SO4 system was studied by the pseudo ternary phase diagram. The electrostatic forces (both attraction and repulsion) between cationic surfactant and anionic surfactant decreased because of the interaction of alcohol hydroxyl group and surfactant polar group. As a result, the phase area width of aqueous two-phase system increased. Long chain alcohol (more than five carbonatoms), which was in high concentration in the SDS/CTAB/H2O/Na2SO4) system, caused the anionic aqueous two-phase system area to vanish and the cationic aqueous two-phase system area to become wider. The CTAB rich phase turned from top phase to bottom phase.

  15. Synthesis of silicon carbide nanowires by solid phase source chemical vapor deposition

    Institute of Scientific and Technical Information of China (English)

    NI Jie; LI Zhengcao; ZHANG Zhengjun

    2007-01-01

    In this paper,we report a simple approach to synthesize silicon carbide(SiC)nanowires by solid phase source chemical vapor deposition(CVD) at relatively low temperatures.3C-SiC nanowires covered by an amorphous shell were obtained on a thin film which was first deposited on silicon substrates,and the nanowires are 20-80 am in diameter and several μm in length,with a growth direction of[200].The growth of the nanowires agrees well on vapor-liquid-solid (VLS)process and the film deposited on the substrates plays an important role in the formation of nanowires.

  16. Analysis of Circularly Polarized Hemispheroidal Dielectric Resonator Antenna Phased Arrays Using the Method of Auxiliary Sources

    DEFF Research Database (Denmark)

    Larsen, Niels Vesterdal; Breinbjerg, Olav

    2007-01-01

    The method of auxiliary sources is employed to model and analyze probe-fed hemispheroidal dielectric resonator antennas and arrays. Circularly polarized antenna elements of different designs are analyzed, and impedance bandwidths of up to 14.7% are achieved. Selected element designs are subsequen...... are subsequently employed in a seven-element phased array. The array performance is analyzed with respect to scan loss and main beam directivity as a function of scan angle and frequency, and the influence of element separation is investigated....

  17. Space Vector Pulse Width Modulation Scheme for a Seven-Phase Voltage Source Inverter

    Directory of Open Access Journals (Sweden)

    Mohd. Arif Khan

    2011-09-01

    Full Text Available This paper analyses a simple space vector PWM (SVPWM scheme for a seven-phase voltage source inverter. At first the conventional method of producing sinusoidal output voltage  by utilizing six active and a zero space vectors are used to synthesis the input reference and then new PWM scheme called time equivalent space vector PWM is presented.  A comparison of the proposed scheme with the conventional scheme is presented based on various performance indices. Extensive Simulation results are provided to validate the findings

  18. Control Strategy for Three Phase Voltage Source PWM Rectifier Based on the Space Vector Modulation

    Directory of Open Access Journals (Sweden)

    MILOUD, Y.

    2010-08-01

    Full Text Available This paper proposes the space vector pulse width modulation (SVPWM control scheme for three-phase voltage source PWM rectifier. The control system based on SVPWM includes two PI controllers which are used to regulate the AC currents and DC-link voltage. The proposed control can stabilize the minimum of the systems storage function at the desired equilibrium point determined by unity power factor and sinusoidal current on the AC side, and constant output voltage on the DC side. So the stable state performance and robustness against the load�s disturbance of PWM rectifiers are both improved. The simulation result shows feasibility of this strategy.

  19. Interrelationship between partition behavior of organic compounds and proteins in aqueous dextran-polyethylene glycol and polyethylene glycol-sodium sulfate two-phase systems.

    Science.gov (United States)

    Ferreira, Luisa A; da Silva, Nuno R; Wlodarczyk, Samarina R; Loureiro, Joana A; Madeira, Pedro P; Teixeira, José A; Uversky, Vladimir N; Zaslavsky, Boris Y

    2016-04-22

    Partition behavior of adenosine and guanine mononucleotides was examined in aqueous dextran-polyethylene glycol (PEG) and PEG-sodium sulfate two-phase systems. The partition coefficients for each series of mononucleotides were analyzed as a functions of the number of phosphate groups and found to be dependent on the nature of nucleic base and on the type of ATPS utilized. It was concluded that an average contribution of a phosphate group into logarithm of partition coefficient of a mononucleotide cannot be used to estimate the difference between the electrostatic properties of the coexisting phases of ATPS. The data obtained in this study were considered together with those for other organic compounds and proteins reported previously, and the linear interrelationship between logarithms of partition coefficients in dextran-PEG, PEG-Na2SO4 and PEG-Na2SO4-0.215M NaCl (all in 0.01M Na- or K/Na-phosphate buffer, pH 7.4 or 6.8) was established. Similar relationship was found for the previously reported data for proteins in Dex-PEG, PEG-600-Na2SO4, and PEG-8000-Na2SO4 ATPS. It is suggested that the linear relationships of the kind established in ATPS may be observed for biological properties of compounds as well.

  20. 手性药物扁桃酸的双水相分离%Study on partition of D(-)-mandelic acid in aqueous two-phase systems

    Institute of Scientific and Technical Information of China (English)

    许小平; 李忠琴; 陈杰波

    2004-01-01

    Studies on the partition of D (-)-mandelic acid were performed in polyethylene glycol (PEG) with molecular masses of 2000, 4000, 6000, 10000, 20000- ammonium sulfate systems. The effect of various parameters such as molecular mass of PEG, phase composition, pH of the system and temperature were investigated in this work. The results indicate that the molecular mass of PEG is a key factor affecting the partitioning behaviors of D(-)-mandelic acid in the PEG -(NH4)2SO4 systems. The influence of pH on the partition shows that the partition coefficient of D(-)-mandelic acid decreases with the increase of pH value. D(-)-mandelic acid partition is only slightly influenced by the temperature. All these indicate that the aqueous two-phase is a very suitable alternative system for the separation of D(-)-mandelic acid.%采用聚乙二醇-硫酸铵双水相系统分离手性药物扁桃酸.研究了聚乙二醇分子量、相组成、pH值和温度对扁桃酸分离的影响.结果表明,聚乙二醇分子量对双水相分离扁桃酸的影响最大;温度对扁桃酸的分离几乎没有影响;随pH增大,扁桃酸分配系数减少.

  1. Analysis of iodinated haloacetic acids in drinking water by reversed-phase liquid chromatography/electrospray ionization/tandem mass spectrometry with large volume direct aqueous injection.

    Science.gov (United States)

    Li, Yongtao; Whitaker, Joshua S; McCarty, Christina L

    2012-07-01

    A large volume direct aqueous injection method was developed for the analysis of iodinated haloacetic acids in drinking water by using reversed-phase liquid chromatography/electrospray ionization/tandem mass spectrometry in the negative ion mode. Both the external and internal standard calibration methods were studied for the analysis of monoiodoacetic acid, chloroiodoacetic acid, bromoiodoacetic acid, and diiodoacetic acid in drinking water. The use of a divert valve technique for the mobile phase solvent delay, along with isotopically labeled analogs used as internal standards, effectively reduced and compensated for the ionization suppression typically caused by coexisting common inorganic anions. Under the optimized method conditions, the mean absolute and relative recoveries resulting from the replicate fortified deionized water and chlorinated drinking water analyses were 83-107% with a relative standard deviation of 0.7-11.7% and 84-111% with a relative standard deviation of 0.8-12.1%, respectively. The method detection limits resulting from the external and internal standard calibrations, based on seven fortified deionized water replicates, were 0.7-2.3 ng/L and 0.5-1.9 ng/L, respectively.

  2. 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.

  3. Water-dispersable hybrid Au-Pd nanoparticles as catalysts in ethanol oxidation, aqueous phase Suzuki-Miyaura and Heck reactions

    KAUST Repository

    Song, HyonMin

    2012-01-01

    The catalytic activities of water-dispersable Au@Pd core-shell nanoparticles (NPs) and Au-Pd alloy NPs were examined. There is growing interest in Au-Pd hybridized NPs in a supported matrix or non-supported forms as catalysts in various reactions that are not limited to conventional Pd-related reactions. Four different Au@Pd core-shell NPs in this study were prepared at room temperature with help from the emulsion phase surrounding the Au core NPs. Au-Pd alloy NPs were prepared over 90 °C, and underwent phase transfer to aqueous medium for their catalytic use. Au@Pd core-shell NPs show catalytic activity in ethanol oxidation reactions as electrocatalysts, and both core-shell and alloy NPs are good to excellent catalysts in various Suzuki-Miyaura and Heck reactions as heterogeneous catalysts. Specifically, Au@Pd core-shell NPs with sharp branched arms show the highest yield in the reactions tested in this study. A relatively small amount (0.25 mol%) was used throughout the catalytic reactions. © 2012 The Royal Society of Chemistry.

  4. Preparation and evaluation of molecularly imprinted solid-phase micro-extraction fibers for selective extraction of phthalates in an aqueous sample

    Energy Technology Data Exchange (ETDEWEB)

    He Juan, E-mail: juanhe@haut.edu.cn [School of Chemistry and Chemical Engineering, Henan University of, Technology, LianHua Road, Zhengzhou 450051 (China); Lv Ruihe; Zhan Haijun; Wang Huizhi; Cheng Jie; Lu Kui; Wang Fengcheng [School of Chemistry and Chemical Engineering, Henan University of, Technology, LianHua Road, Zhengzhou 450051 (China)

    2010-07-26

    A novel molecularly imprinted polymer (MIP) that was applied to a solid-phase micro-extraction (SPME) device, which could be coupled directly to gas chromatograph and mass spectrometer (GC/MS), was prepared using dibutyl phthalate (DBP) as the template molecule. The characteristics and application of this fiber were investigated. Electron microscope images indicated that the MIP-coated solid-phase micro-extraction (MI-SPME) fibers were homogeneous and porous. The extraction yield of DBP with the MI-SPME fibers was higher than that of the non-imprinted polymer (NIP)-coated SPME (NI-SPME) fibers. The MI-SPME fibers had a higher selectivity to other phthalates that had similar structures as DBP. A method was developed for the determination of phthalates using MI-SPME fibers coupled with GC/MS. The extraction conditions were optimized. Detection limits for the phthalate samples were within the range of 2.17-20.84 ng L{sup -1}. The method was applied to five kinds of phthalates dissolved in spiked aqueous samples and resulted in recoveries of up to 94.54-105.34%, respectively. Thus, the MI-SPME fibers are suitable for the extraction of trace phthalates in complicated samples.

  5. Effect of the vapor phase on the salinity of halite-bearing aqueous fluid inclusions estimated from the halite dissolution temperature

    Science.gov (United States)

    Steele-MacInnis, Matthew; Bodnar, Robert J.

    2013-08-01

    Salinities of aqueous fluid inclusions are commonly determined by measuring the temperatures of dissolution of solid phases (daughter minerals) during heating. The vapor bubble is, in most cases, considered to have no mass and to have no effect on the bulk salinity, owing to the low density of the vapor. In the present study we test the assumption that the vapor bubble can be ignored when estimating salinity based on the halite dissolution temperature. The errors in bulk salinity that result from neglecting the vapor bubble are generally less than ˜1.5 wt.% NaCl, and errors of this magnitude occur only when there is a large difference between the halite dissolution temperature and the vapor disappearance temperature (e.g., halite dissolution at ˜450 °C and vapor bubble disappearance at 800 °C) or, stated differently, when the vapor bubble occupies a significant volume fraction of the inclusion at the temperature of halite disappearance. In most cases errors are less than 0.5 wt.% NaCl. Salinity estimated based on Tm,H can be adjusted to account for the contribution of H2O from the vapor phase, using an empirical relationship describing the proportion of liquid in the inclusion at Tm,H as a function of the difference between Th,LV and Tm,H.

  6. Interrelationship between partition behavior of organic compounds and proteins in aqueous dextran-polyethylene glycol and polyethylene glycol-sodium sulfate two-phase systems.

    Science.gov (United States)

    Ferreira, Luisa A; da Silva, Nuno R; Wlodarczyk, Samarina R; Loureiro, Joana A; Madeira, Pedro P; Teixeira, José A; Uversky, Vladimir N; Zaslavsky, Boris Y

    2016-04-22

    Partition behavior of adenosine and guanine mononucleotides was examined in aqueous dextran-polyethylene glycol (PEG) and PEG-sodium sulfate two-phase systems. The partition coefficients for each series of mononucleotides were analyzed as a functions of the number of phosphate groups and found to be dependent on the nature of nucleic base and on the type of ATPS utilized. It was concluded that an average contribution of a phosphate group into logarithm of partition coefficient of a mononucleotide cannot be used to estimate the difference between the electrostatic properties of the coexisting phases of ATPS. The data obtained in this study were considered together with those for other organic compounds and proteins reported previously, and the linear interrelationship between logarithms of partition coefficients in dextran-PEG, PEG-Na2SO4 and PEG-Na2SO4-0.215M NaCl (all in 0.01M Na- or K/Na-phosphate buffer, pH 7.4 or 6.8) was established. Similar relationship was found for the previously reported data for proteins in Dex-PEG, PEG-600-Na2SO4, and PEG-8000-Na2SO4 ATPS. It is suggested that the linear relationships of the kind established in ATPS may be observed for biological properties of compounds as well. PMID:27016118

  7. A single-phase embedded Z-source DC-AC inverter.

    Science.gov (United States)

    Kim, Se-Jin; Lim, Young-Cheol

    2014-01-01

    In the conventional DC-AC inverter consisting of two DC-DC converters with unipolar output capacitors, the output capacitor voltages of the DC-DC converters must be higher than the DC input voltage. To overcome this weakness, this paper proposes a single-phase DC-AC inverter consisting of two embedded Z-source converters with bipolar output capacitors. The proposed inverter is composed of two embedded Z-source converters with a common DC source and output AC load. Though the output capacitor voltages of the converters are relatively low compared to those of a conventional inverter, an equivalent level of AC output voltages can be obtained. Moreover, by controlling the output capacitor voltages asymmetrically, the AC output voltage of the proposed inverter can be higher than the DC input voltage. To verify the validity of the proposed inverter, experiments were performed with a DC source voltage of 38 V. By controlling the output capacitor voltages of the converters symmetrically or asymmetrically, the proposed inverter can produce sinusoidal AC output voltages. The experiments show that efficiencies of up to 95% and 97% can be achieved with the proposed inverter using symmetric and asymmetric control, respectively.

  8. A single-phase embedded Z-source DC-AC inverter.

    Science.gov (United States)

    Kim, Se-Jin; Lim, Young-Cheol

    2014-01-01

    In the conventional DC-AC inverter consisting of two DC-DC converters with unipolar output capacitors, the output capacitor voltages of the DC-DC converters must be higher than the DC input voltage. To overcome this weakness, this paper proposes a single-phase DC-AC inverter consisting of two embedded Z-source converters with bipolar output capacitors. The proposed inverter is composed of two embedded Z-source converters with a common DC source and output AC load. Though the output capacitor voltages of the converters are relatively low compared to those of a conventional inverter, an equivalent level of AC output voltages can be obtained. Moreover, by controlling the output capacitor voltages asymmetrically, the AC output voltage of the proposed inverter can be higher than the DC input voltage. To verify the validity of the proposed inverter, experiments were performed with a DC source voltage of 38 V. By controlling the output capacitor voltages of the converters symmetrically or asymmetrically, the proposed inverter can produce sinusoidal AC output voltages. The experiments show that efficiencies of up to 95% and 97% can be achieved with the proposed inverter using symmetric and asymmetric control, respectively. PMID:25133241

  9. A Novel Family of Catalysts Comprising a Supported Metal and a Supported Aqueous-Phase Catalyst%新型复合负载金属-支撑水相催化剂

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    @@ The interface between homogeneous catalysis and heterogeneous catalysis has great scope for the development of new catalytic materials[1~4]. Supported aqueous-phase (SAP) catalysis has been employed for the hydroformylation of olefins under mild conditions with high efficiency and convenient separation from the products[5,6].

  10. 非水相酶催化技术在食品添加剂生产中的应用%Advances in Application of Non-aqueous Phase Enzymatic Catalysis in Food Additive Production

    Institute of Scientific and Technical Information of China (English)

    余泗莲; 余琳; 余彬; 孙文敬; 刘长峰; 杨梦依; 崔凤杰

    2013-01-01

    非水相催化技术已在食品添加剂生产中得到广泛应用.综述了非水相酶催化反应介质的种类,主要介绍了该技术在(异)抗坏血酸酯、短链酸酯、糖酯、维生素A酯和维生素E酯等食品添加剂合成中的应用.最后对非水相酶催化技术的前景进行了展望.%Non-aqueous phase enzymatic catalysis technology has been widely applied in the area of food additives production.This paper reviewed the types of reaction medium of non-aqueous phase enzymatic catalysis reaction,introduced the application of non-aqueous phase enzymatic catalysis technology in catalysis of L-ascorbic (isoascorbic) acid esters,short-chain acid esters,sugar esters,vitamin A esters,vitamin E esters,and other food additives,and finally predicted the prospects of non-aqueous phase enzymatic catalysis technology.

  11. Evaluation of Aqueous and Powder Processing Techniques for Production of Pu-238-Fueled General Purpose Heat Sources

    Energy Technology Data Exchange (ETDEWEB)

    2008-06-01

    This report evaluates alternative processes that could be used to produce Pu-238 fueled General Purpose Heat Sources (GPHS) for radioisotope thermoelectric generators (RTG). Fabricating GPHSs with the current process has remained essentially unchanged since its development in the 1970s. Meanwhile, 30 years of technological advancements have been made in the fields of chemistry, manufacturing, ceramics, and control systems. At the Department of Energy’s request, alternate manufacturing methods were compared to current methods to determine if alternative fabrication processes could reduce the hazards, especially the production of respirable fines, while producing an equivalent GPHS product. An expert committee performed the evaluation with input from four national laboratories experienced in Pu-238 handling.

  12. Electrical and Thermal Behavior of Copper-Epoxy Nanocomposites Prepared via Aqueous to Organic Phase Transfer Technique

    Directory of Open Access Journals (Sweden)

    N. H. Mohd Hirmizi

    2012-01-01

    Full Text Available The preparation, electrical, and thermal behaviors of copper-epoxy nanocomposites are described. Cetyltrimethylammonium bromide- (CTAB- stabilized copper (Cu particles were synthesized via phase transfer technique. Isopropanol (IPA, sodium borohydride (NaBH4, and toluene solution of diglycidyl ether of bisphenol A (DGEBA were used as transferring, reducing agent, and the organic phase, respectively. The UV-Vis absorbance spectra of all the sols prepared indicate that the presence of Cu particles with the particles transfer efficiency is ≥97%. The amount, size, and size distribution of particles in the organosol were dependent on the content of organic solute in the organosol. The composites were obtained upon drying the organosols and these were then subjected to further studies on the curing, thermal, and electrical characteristic. The presence of Cu fillers does not significantly affect the completeness of the composite curing process and only slightly reduce the thermal stability of the composites that is >300°C. The highest conductivity value of the composites obtained is 3.06×10-2 S cm-1.

  13. Power sharing algorithm for vector controlled six-phase AC motor with four customary three-phase voltage source inverter drive

    DEFF Research Database (Denmark)

    Padmanaban, Sanjeevikumar; Grandi, Gabriele; Blaabjerg, Frede;

    2015-01-01

    This paper considered a six-phase (asymmetrical) induction motor, kept 30 phase displacement between two set of three-phase open-end stator windings configuration. The drive system consists of four classical three-phase voltage inverters (VSIs) and all four dc sources are deliberately kept isolated......) by nearest three vectors (NTVs) approach is adopted to regulate each couple of VSIs. The proposed power sharing algorithm is verified by complete numerical simulation modeling (Matlab/ Simulink-PLECS software) of whole ac drive system by observing the dynamic behaviors in different designed condition. Set...

  14. Structure and sources of solar wind in the growing phase of 24th solar cycle

    Science.gov (United States)

    Slemzin, Vladimir; Goryaev, Farid; Shugay, Julia; Rodkin, Denis; Veselovsky, Igor

    2015-04-01

    We present analysis of the solar wind (SW) structure and its association with coronal sources during the minimum and rising phase of 24th solar cycle (2009-2011). The coronal sources prominent in this period - coronal holes, small areas of open magnetic fields near active regions and transient sources associated with small-scale solar activity have been investigated using EUV solar images and soft X-ray fluxes obtained by the CORONAS-Photon/TESIS/Sphinx, PROBA2/SWAP, Hinode/EIS and AIA/SDO instruments as well as the magnetograms obtained by HMI/SDO. It was found that at solar minimum (2009) velocity and magnetic field strength of high speed wind (HSW) and transient SW from small-scale flares did not differ significantly from those of the background slow speed wind (SSW). The major difference between parameters of different SW components was seen in the ion composition represented by the C6/C5, O7/O6, Fe/O ratios and the mean charge of Fe ions. With growing solar activity, the speed of HSW increased due to transformation of its sources - small-size low-latitude coronal holes into equatorial extensions of large polar holes. At that period, the ion composition of transient SW changed from low-temperature to high-temperature values, which was caused by variation of the source conditions and change of the recombination/ionization rates during passage of the plasma flow through the low corona. However, we conclude that criteria of separation of the SW components based on the ion ratios established earlier by Zhao&Fisk (2009) for higher solar activity are not applicable to the extremely weak beginning of 24th cycle. The research leading to these results has received funding from the European Commission's Seventh Framework Programme (FP7/2007-2013) under the grant agreement eHeroes (project n° 284461, www.eheroes.eu).

  15. Antifungal activity of clotrimazole against Candida albicans depends on carbon sources, growth phase and morphology.

    Science.gov (United States)

    Kasper, Lydia; Miramón, Pedro; Jablonowski, Nadja; Wisgott, Stephanie; Wilson, Duncan; Brunke, Sascha; Hube, Bernhard

    2015-07-01

    Vulvovaginal candidiasis, a superficial infection caused predominantly by the pathogenic fungus Candida albicans, is frequently treated with clotrimazole. Some drug formulations contain lactate for improved solubility. Lactate may modify C. albicans physiology and drug sensitivity by serving as a carbon source for the fungus and/or affecting local pH. Here, we explored the effects of lactate, in combination with pH changes, on C. albicans proliferation, morphology and clotrimazole sensitivity. Moreover, we determined the influence of growth phase and morphology per se on drug sensitivity. We showed that utilization of lactate as a carbon source did not promote fast fungal proliferation or filamentation. Lactate had no influence on clotrimazole-mediated killing of C. albicans in standard fungal cultivation medium but had an additive effect on the fungicidal clotrimazole action under in vitro vagina-simulative conditions. Moreover, clotrimazole-mediated killing was growth-phase and morphology dependent. Post-exponential cells were resistant to the fungicidal action of clotrimazole, whilst logarithmic cells were sensitive, and hyphae showed the highest susceptibility. Finally, we showed that treatment of pre-formed C. albicans hyphae with sublethal concentrations of clotrimazole induced a reversion to yeast-phase growth. As C. albicans hyphae are considered the pathogenic morphology during mucosal infections, these data suggest that elevated fungicidal activity of clotrimazole against hyphae plus clotrimazole-induced hyphae-to-yeast reversion may help to dampen acute vaginal infections by reducing the relative proportion of hyphae and thus shifting to a non-invasive commensal-like population. In addition, lactate as an ingredient of clotrimazole formulations may potentiate clotrimazole killing of C. albicans in the vaginal microenvironment. PMID:25976001

  16. Site Characterization of the Source Physics Experiment Phase II Location Using Seismic Reflection Data

    Science.gov (United States)

    Sexton, E. A.; Snelson, C. M.; Chipman, V.; Emer, D. F.; White, R. L.; Emmitt, R.; Wright, A. A.; Drellack, S.; Huckins-Gang, H.; Mercadante, J.; Floyd, M.; McGowin, C.; Cothrun, C.; Bonal, N.

    2013-12-01

    An objective of the Source Physics Experiment (SPE) is to identify low-yield nuclear explosions from a regional distance. Low-yield nuclear explosions can often be difficult to discriminate among the clutter of natural and man-made explosive events (e.g., earthquakes and mine blasts). The SPE is broken into three phases. Phase I has provided the first of the physics-based data to test the empirical models that have been used to discriminate nuclear events. The Phase I series of tests were placed within a highly fractured granite body. The evolution of the project has led to development of Phase II, to be placed within the opposite end member of geology, an alluvium environment, thereby increasing the database of waveforms to build upon in the discrimination models. Both the granite and alluvium sites have hosted nearby nuclear tests, which provide comparisons for the chemical test data. Phase III of the SPE is yet to be determined. For Phase II of the experiment, characterization of the location is required to develop the geologic/geophysical models for the execution of the experiment. Criteria for the location are alluvium thickness of approximately 170 m and a water table below 170 m; minimal fracturing would be ideal. A P-wave mini-vibroseis survey was conducted at a potential site in alluvium to map out the subsurface geology. The seismic reflection profile consisted of 168 geophone stations, spaced 5 m apart. The mini-vibe was a 7,000-lb peak-force source, starting 57.5 m off the north end of the profile and ending 57.5 m past the southern-most geophone. The length of the profile was 835 m. The source points were placed every 5 m, equally spaced between geophones to reduce clipping. The vibroseis sweep was from 20 Hz down to 180 Hz over 8 seconds, and four sweeps were stacked at each shot location. The shot gathers show high signal-to-noise ratios with clear first arrivals across the entire spread and the suggestion of some shallow reflectors. The data were

  17. Preparation of CdS Nanoparticles in Aqueous Phase and Photocatalytic Degradation of Rhodamine B%硫化镉纳米粒子的水相制备及光催化降解罗丹明B

    Institute of Scientific and Technical Information of China (English)

    黄正喜; 杜锴; 胡振龙

    2012-01-01

    CdS nanoparticles were successfully prepared by a precipitation method in aqueous phase,cadmium chloride and thiosemicarbazide were used as cadmium and sulfur sources respectively.The CdS nanoparticles were characterized by X-ray diffraction(XRD),X-ray photoelectron spectroscopy(XPS),scanning electron microscope(SEM),transmission electron microscope(TEM) and UV-Vis spectrum.The photocatalytic degradation of Rhodamine B(RhB) under visible light was used as probe reactions to evaluate the photocatalytic activities of the prepared nanopartiles.The results indicated that the preparation method is simple,and the products have high photocatalytic activity.%以氯化镉为镉源,硫代氨基脲为硫源,在水相中通过沉淀法制备出硫化镉纳米颗粒,并对其进行表征.以光催化降解罗丹明B作为探针反应,评价其光催化降解活性.结果表明:该制备方法简单易行,所得纳米粒子具有良好的光催化活性.

  18. High yield of pentane production by aqueous-phase reforming of xylitol over Ni/HZSM-5 and Ni/MCM22 catalysts

    International Nuclear Information System (INIS)

    Graphical abstract: Ni/HZSM-5 and Ni/MCM22 catalysts were developed with remarkable pentane yield of 90–95% for aqueous-phase reforming of xylitol. Pentane can be selectively generated by adjusting the Ni loading and acid amount of the catalyst. The Ni/MCM22 catalyst exhibited excellent stability ever after five recycle runs, while the Ni/HZSM-5 catalyst deactivated significantly. Display Omitted Highlights: ► Development of Ni/HZSM-5 and Ni/MCM22 catalyst with remarkable catalytic activity. ► High pentane production by optimizing the Ni loading of the catalyst. ► Excellent stability of Ni/MCM22 catalyst under the hydrothermal condition. - Abstract: Ni/HZSM-5 and Ni/MCM22 catalysts with different Ni loadings were prepared by impregnation method and evaluated for aqueous-phase reforming (APR) reaction of xylitol at 240 °C and 4 MPa. Effects of Ni loadings on the xylitol conversion and pentane selectivity of the catalyst was investigated. The results showed that the catalytic activities of the two Ni/HZSM-5 and Ni/MCM22 catalysts both increased with increasing Ni loading in the range of 0–2%, and then decreased as Ni loading further increased to 4%. Maximum pentane yields of 91% and 95% could be obtained over 2%Ni/HZSM-5 and 2%Ni/MCM22, respectively. 2%Ni/HZSM-5 deactivated obviously after five recycle runs, while 2%Ni/MCM22 still kept excellent activity with the pentane yield of 90–95%. The catalysts with different Ni loading were characterized by BET, H2-TPR and NH3-TPD techniques and the used selected 2%Ni/MCM22 and 2%Ni/HZSM-5 catalyst were also characterized by XRD, FTIR and TG. The characterization results revealed that 2%Ni/MCM22 and 2%Ni/HZSM-5 have similar amounts of Ni active sites, while the 2%Ni/MCM22 has larger surface area, more mesopore and less strong acid sites than the 2%Ni/HZSM-5. Moreover, partial dealumination and coke formation of the used 2%Ni/HZSM-5 catalyst were found. All these factors resulted in the deactivation of 2%Ni/HZSM-5

  19. Single-phase Multilevel Current Source Inverter with Reduced Device Count and Current Balancing Capability

    Directory of Open Access Journals (Sweden)

    MOALLEMI KHIAVI, A.

    2015-08-01

    Full Text Available Nowadays power converters play an important role in power system and industrial centers. One of the most important and widely used types of conversion is DC to AC conversion that is also called inverters. Generally inverters are divided to voltage source inverter (VSI and current source inverter (CSI. From another view the inverters are divided to two-level and multilevel types. The multilevel inverters are attractive because of their good output waveform quality. However, there has been less attention to multilevel current source inverter (MLCSI when compared with multilevel VSI. In this paper, a new topology for MLCSI is proposed. The proposed topology employs reduced number of switches to generate desired multilevel output current. The proposed MLCSI is capable of balancing the currents of the inductors that are used in the MLCSI structure. A multicarrier PWM based switching strategy is also proposed for the MLCSI. The simulation results using PSCAD/EMTDC as well as the experimental results from a single-phase 5-level CSI laboratory prototype demonstrate its validity.

  20. 28 MHz swept source at 1.0 μm for ultrafast quantitative phase imaging.

    Science.gov (United States)

    Wei, Xiaoming; Lau, Andy K S; Xu, Yiqing; Tsia, Kevin K; Wong, Kenneth K Y

    2015-10-01

    Emerging high-throughput optical imaging modalities, in particular those providing phase information, necessitate a demanding speed regime (e.g. megahertz sweep rate) for those conventional swept sources; while an effective solution is yet to be demonstrated. We demonstrate a stable breathing laser as inertia-free swept source (BLISS) operating at a wavelength sweep rate of 28 MHz, particularly for the ultrafast interferometric imaging modality at 1.0 μm. Leveraging a tunable dispersion compensation element inside the laser cavity, the wavelength sweep range of BLISS can be tuned from ~10 nm to ~63 nm. It exhibits a good intensity stability, which is quantified by the ratio of standard deviation to the mean of the pulse intensity, i.e. 1.6%. Its excellent wavelength repeatability, <0.05% per sweep, enables the single-shot imaging at an ultrafast line-scan rate without averaging. To showcase its potential applications, it is applied to the ultrafast (28-MHz line-scan rate) interferometric time-stretch (iTS) microscope to provide quantitative morphological information on a biological specimen at a lateral resolution of 1.2 μm. This fiber-based inertia-free swept source is demonstrated to be robust and broadband, and can be applied to other established imaging modalities, such as optical coherence tomography (OCT), of which an axial resolution better than 12 μm can be achieved. PMID:26504636