A new polymeric adsorbent developing for uranium recovering and richment from aqueous media

International Nuclear Information System (INIS)

Gueler, H.; Aycik, G. A.; Sahiner, N.; Gueven, O.

1997-01-01

Using adsorbents is thought to be the most effective method for recovering the low concentrations of uranium in the aqueous media because of their fast and selective uptake of uranium, a sufficient adsorption capacity and high physical and chemical stability against the media. In this study, a new polymeric adsorbent bearing both hydrophilic groups providing swelling in water and amidoxime groups for chelating with uranyl ions (UO 2 ''2+) has been developed and its adsorptive ability for uranium from aqueous media has been investigated. The polymers obtained by irradiating the solution of polyethylene glycol (PEG) in acrylonitrile (AN) are defined as Interpenetrating Polymer Networks (IPNs) and the adsorbent has been obtained by applying the amidoximation reaction to the IPNs with a conversion of % 60 approximately. Kinetics of the conversion reaction of nitrile (CN) group to amidoxime (HONCNH 2 ) group has been studied by reacting with hydroxylamine (NH 2 OH) solution at a molar ratio of NH 2 OH/CN=1.25 in aqueous media at different temperatures, 30,40,50''0C, for 3-4 days. The degree of amidoximation was determined by UO 2 ''2+ ion adsorption and FTIR spectrometer and the UO 2 ''2+ ion adsorption values were found by both UV and gamma spectrometry and also by gravimetry. It was found that the polymeric adsorbent has a very high adsorption ability for uranium (∼ 540 mg U/g IPN/day)

Scripting Fonetico nuove risorse per leggere il greco antico mediante la sintesi vocale

Directory of Open Access Journals (Sweden)

Silvia Gianferrari

2011-04-01

Full Text Available Lo scripting fonetico da lingua italiana produce finalmente una sintesi vocale del greco antico senz’altro soddisfacente per gli usi didattici della Scuola secondaria, per l’accesso alle banche dati che raccolgono l’intero patrimonio letterario della lingua antica e per l’editoria digitale costruita secondo i parametri dell’accessibilità.

Extraction from aqueous media novocaine aliphatic alcohols using salting out agent

Directory of Open Access Journals (Sweden)

Y. I. Korenman

2012-01-01

Full Text Available The choice of rational conditions for the extraction of novocaine. Development of effective extraction systems for almost its complete removal from aqueous media. Establishing correlations between coefficients distribution (lgD novocaine and the number of C–atoms in a molecule of alcohol.

Behaviour of polycrystalline fluoride-selective membrane electrode in aqueous-organic media

International Nuclear Information System (INIS)

Manakova, L.I.; Bausova, N.V.; Moiseev, V.E.; Bamburov, V.G.; Sivoplyas, A.P.

1978-01-01

The behaviour of polycrystalline fluoride membrane electrode (RFME) in aqueous-organic media has been studied when the content of the organic component (methanol, ethanol, acetone, dioxane) has been changed from 20 to 80 mass%. Since LaF 3 is the base of the membrane, its solubility has been studied depending on the organic component content in the solution. It has been established that LaF 3 solubility decreases with increasing content of of the organic component. This explains the effect of the composition of an aqueous-organic solvent on the electrode sensitivity. The electrode sensitivity rises with increasing content of the organic component in an aqueous-organic solvent. A greater decrease of LaF 3 solubility in aqueous-organic solvents as compared with that of LaCl 3 , La(NO 3 ) 3 , and La 2 (SO 4 ) 3 causes a higher selectivity of RFME with respect to the anions under study

Aqueous media treatment and decontamination of hazardous chemical and biological substances by contact plasma

International Nuclear Information System (INIS)

Pivovarov, A.; Kravchenko, A.; Kublanovsky, V.

2009-01-01

Usage of non-equilibrium contact plasma for processes of decontamination and neutralization in conditions of manifestation of chemical, biological and radiation terrorism takes on special significance due to portability of equipment and its mobility in places where toxic liquid media hazardous for people's health are located. Processes of decontamination of aqueous media, seminated with pathogenic microorganisms and viruses, treatment of water containing toxic heavy metals, cyanides, surface-active substances, and heavy radioactive elements, are investigated. Examples of activation processes in infected water and toxic aqueous solutions present convincing evidence of the way, how new quality technological approach for achievement of high enough degree of the said media treatment is used in each specific case. Among new properties of water activated as a result of action of non-equilibrium contact plasma, it is necessary to mention presence of cluster structure, confirmed by well-known spectral and physical-chemical methods, presence of peroxide compounds, active particles and radicals. Anti-microbial activity which is displayed under action of plasma in aqueous media (chemically pure water, drinking water, aqueous solutions of sodium chloride, potassium iodide, as well as other inorganic compounds) towards wide range of pathogenic and conventionally pathogenic microorganisms allows use them as reliable, accessible and low-cost preparations for increasing the degree of safety of food products. Combination of such processes with known methods of filtration and ultra-filtration gives an efficient and available complex capable of withstanding any threats, which may arise for population and living organisms. Present-day level of machine-building, electrical engineering, and electronics allows predict creation of industrial plasma installations, adapted to conditions of various terrorist threats, with minimized power consumption and optimized technological parameters

Aqueous media treatment and decontamination of hazardous chemical and biological substances by contact plasma

Energy Technology Data Exchange (ETDEWEB)

Pivovarov, A; Kravchenko, A [Ukrainian State University of Chemical Engineering, Dnepropetrovsk (Ukraine); Kublanovsky, V [V. I. Vernadsky Institute of General and Inorganic Chemistry of National Academy of Science, Kiev (Ukraine)

2009-07-01

Usage of non-equilibrium contact plasma for processes of decontamination and neutralization in conditions of manifestation of chemical, biological and radiation terrorism takes on special significance due to portability of equipment and its mobility in places where toxic liquid media hazardous for people's health are located. Processes of decontamination of aqueous media, seminated with pathogenic microorganisms and viruses, treatment of water containing toxic heavy metals, cyanides, surface-active substances, and heavy radioactive elements, are investigated. Examples of activation processes in infected water and toxic aqueous solutions present convincing evidence of the way, how new quality technological approach for achievement of high enough degree of the said media treatment is used in each specific case. Among new properties of water activated as a result of action of non-equilibrium contact plasma, it is necessary to mention presence of cluster structure, confirmed by well-known spectral and physical-chemical methods, presence of peroxide compounds, active particles and radicals. Anti-microbial activity which is displayed under action of plasma in aqueous media (chemically pure water, drinking water, aqueous solutions of sodium chloride, potassium iodide, as well as other inorganic compounds) towards wide range of pathogenic and conventionally pathogenic microorganisms allows use them as reliable, accessible and low-cost preparations for increasing the degree of safety of food products. Combination of such processes with known methods of filtration and ultra-filtration gives an efficient and available complex capable of withstanding any threats, which may arise for population and living organisms. Present-day level of machine-building, electrical engineering, and electronics allows predict creation of industrial plasma installations, adapted to conditions of various terrorist threats, with minimized power consumption and optimized technological parameters

Spontaneous and Directional Bubble Transport on Porous Copper Wires with Complex Shapes in Aqueous Media.

Science.gov (United States)

Li, Wenjing; Zhang, Jingjing; Xue, Zhongxin; Wang, Jingming; Jiang, Lei

2018-01-24

Manipulation of gas bubble behaviors is crucial for gas bubble-related applications. Generally, the manipulation of gas bubble behaviors generally takes advantage of their buoyancy force. It is very difficult to control the transportation of gas bubbles in a specific direction. Several approaches have been developed to collect and transport bubbles in aqueous media; however, most reliable and effective manipulation of gas bubbles in aqueous media occurs on the interfaces with simple shapes (i.e., cylinder and cone shapes). Reliable strategies for spontaneous and directional transport of gas bubbles on interfaces with complex shapes remain enormously challenging. Herein, a type of 3D gradient porous network was constructed on copper wire interfaces, with rectangle, wave, and helix shapes. The superhydrophobic copper wires were immersed in water, and continuous and stable gas films then formed on the interfaces. With the assistance of the Laplace pressure gradient between two bubbles, gas bubbles (including microscopic gas bubbles) in the aqueous media were subsequently transported, continuously and directionally, on the copper wires with complex shapes. The small gas bubbles always moved to the larger ones.

Effect of passivation on the sensitivity and stability of pentacene transistor sensors in aqueous media

KAUST Repository

Khan, Hadayat Ullah

2011-06-01

Charge-detecting biosensors have recently become the focal point of biosensor research, especially research onto organic thin-film transistors (OTFTs), which combine compactness, a low cost, and fast and label-free detection to realize simple and stable in vivo diagnostic systems. We fabricated organic pentacene-based bottom-contact thin-film transistors with an ultra-thin insulating layer of a cyclized perfluoro polymer called CYTOP (Asahi Glass Co., Tokyo, Japan) on SiO2 for operation in aqueous media. The stability and sensitivity of these transistor sensors were examined in aqueous buffer media with solutions of variable pH levels after the passivation of perfluoro polymers with thicknesses ranging from 50 to 300nm. These transistor sensors were further modified with an ultra-thin film (5nm) functional layer for selective BSA/antiBSA detection in aqueous buffer media, demonstrating a detection capability as low as 500nM of concentrated antiBSA. The dissociation constant from the antiBSA detection results was 2.1×10-6M. Thus, this study represents a significant step forward in the development of organic electronics for a disposable and versatile chemical and bio-sensing platform. © 2011 Elsevier B.V.

Recovery of homogeneous polyoxometallate catalysts from aqueous and organic media by a mesoporous ceramic membrane without loss of catalytic activity

NARCIS (Netherlands)

Roy Chowdhury, S.; Roy Chowdhury, Sankhanilay; Witte, Peter T.; Blank, David H.A.; Alsters, Paul L.; ten Elshof, Johan E.

2006-01-01

The recovery of homogeneous polyoxometallate (POM) oxidation catalysts from aqueous and non-aqueous media by a nanofiltration process using mesoporous γ-alumina membranes is reported. The recovery of Q12[WZn3(ZnW9O34)2] (Q=[MeN(n-C8H17)3]+) from toluene-based media was quantitative within

Boric Acid Catalyzed Convenient Synthesis of Benzimidazoles in Aqueous Media

Directory of Open Access Journals (Sweden)

Mohammad Reza Poor Heravi

2013-01-01

Full Text Available Synthesis of benzimidazoles has been developed by the o-phenylenediamine with aldehydes using boric acid an efficient catalyst under mild reaction conditions in aqueous media. The product is applicable to aryl and heteroaryl aldehydes. This reaction led to the formation of benzimidazoles new derivatives in good yields. The FT-IR, 19F-NMR, 1H-NMR, 13C-NMR spectra and elemental analysis confirm the structure of compounds.

Boric Acid Catalyzed Convenient Synthesis of Benzimidazoles in Aqueous Media

OpenAIRE

Poor Heravi, Mohammad Reza; Ashori, Marjan

2013-01-01

Synthesis of benzimidazoles has been developed by the o-phenylenediamine with aldehydes using boric acid an efficient catalyst under mild reaction conditions in aqueous media. The product is applicable to aryl and heteroaryl aldehydes. This reaction led to the formation of benzimidazoles new derivatives in good yields. The FT-IR, 19F-NMR, 1H-NMR, 13C-NMR spectra and elemental analysis confirm the structure of compounds.

Oxytetracycline recovery from aqueous media using computationally designed molecularly imprinted polymers.

Science.gov (United States)

Rodríguez-Dorado, Rosalía; Carro, Antonia M; Chianella, Iva; Karim, Kal; Concheiro, Angel; Lorenzo, Rosa A; Piletsky, Sergey; Alvarez-Lorenzo, Carmen

2016-09-01

Polymers for recovery/removal of the antimicrobial agent oxytetracycline (OTC) from aqueous media were developed with use of computational design and molecular imprinting. 2-Hydroxyethyl methacrylate, 2-acrylamide-2-methylpropane sulfonic acid (AMPS), and mixtures of the two were chosen according to their predicted affinity for OTC and evaluated as functional monomers in molecularly imprinted polymers and nonimprinted polymers. Two levels of AMPS were tested. After bulk polymerization, the polymers were crushed into particles (200-1000 μm). Pressurized liquid extraction was implemented for template removal with a low amount of methanol (less than 20 mL in each extraction) and a few extractions (12-18 for each polymer) in a short period (20 min per extraction). Particle size distribution, microporous structure, and capacity to rebind OTC from aqueous media were evaluated. Adsorption isotherms obtained from OTC solutions (30-110 mg L(-1)) revealed that the polymers prepared with AMPS had the highest affinity for OTC. The uptake capacity depended on the ionic strength as follows: purified water > saline solution (0.9 % NaCl) > seawater (3.5 % NaCl). Polymer particles containing AMPS as a functional monomer showed a remarkable ability to clean water contaminated with OTC. The usefulness of the stationary phase developed for molecularly imprinted solid-phase extraction was also demonstrated. Graphical Abstract Selection of functional monomers by molecular modeling renders polymer networks suitable for removal of pollutants from contaminated aqueous environments, under either dynamic or static conditions.

1-N-aminoindol derivatives synthesis in no aqueous means from the 1, 4-dihydrocinnoline obtained by electrolysis in continuous flow redox cell; Sintesis de derivados del 1-N-aminoindol en medios no acuosos a partir de la 1, 4-dihidrocinolina obtenida por electrolisis en celda redox de flujo continuo

Energy Technology Data Exchange (ETDEWEB)

Frontana-Uribe, Bernardo A. [Universidad Nacional Autonoma de Mexico, Mexico, D.F. (Mexico); Moinet, Claude [Laboratoire d' Electrochimie et Organometalliques UMR, Paris (France)

1999-08-01

This work describes the synthesis of 1-N-aminoindol derivatives in organic anhydrous media from 1, 4-dihydrocinnoline. 1, 4-dihydrocinnoline 4 is obtained by electrolysis of 2-(orto-notropheny)-ethylamine 1a in a continuous flow redox cell. The cinnoline ring contraction products are obtained in low yield, but they show the possibility to carry out the reaction in organic media without water addition, as it was noted in previous works. [Spanish] En este trabajo se describe la sintesis de derivados del 1-N-aminoindol en medios anhidros a partir de la 1, 4-dihidrocinolina 4. Esta se obtiene mediante la electrolisis de la 2-(orto-notrofenil)-etilamina 1a en celda redox de flujo continuo. Los productos de contraccion del ciclo de la cinolina en 1-N-aminoindol se obtiene en rendimiento bajo, pero demuestran la posibilidad de llevar a cabo esta reaccion en medios totalmente organicos, sin la necesidad de la adicion de agua en el medio de reaccion, como esta descrito en trabajos precedentes.

SINTESIS NANOPARTIKEL PERAK MENGGUNAKAN METODE POLIOL DENGAN AGEN STABILISATOR POLIVINILALKOHOL (PVA

Directory of Open Access Journals (Sweden)

DOB Apriandanu

2014-06-01

Full Text Available Abstrak __________________________________________________________________________________________ Nanopartikel perak merupakan produk berbasis nanoteknologi yang sedang berkembang saat ini dan dapat diaplikasikan sebagai katalis dan detektor sensor optik. Faktor yang dapat mempengaruhi ukuran nanopartikel adalah konsentrasi garam dan agen pereduksi. Nanopartikel perak bersifat tidak stabil. Oleh karena itu, perlu adanya penambahan polivinil alkohol sebagai agen stabilisator dalam sintesis nanopartikel perak. Tujuan penelitian ini adalah untuk mengetahui pengaruh rasio mol reduktor EG/Ag+ dan % PVA (b/v dalam sintesis nanopartikel perak terhadap karakteristik produk yang dihasilkan. Nanopartikel perak disintesis dengan metode poliol yaitu melarutkan AgNO3 ke dalam etilen glikol sebagai reduktor dan polivinilalkohol (PVA sebagai stabilisator. Karakterisasi dilakukan menggunakan Spek-trofotometer UV-Vis dan TEM (Transmission Electron Microscope. Analisis terhadap spektra UV-Vis menunjukkan bahwa nanopartikel yang relatif stabil pada pengukuran panjang gelombang maksimum 417 hingga 418 nm adalah nanopartikel yang disintesis menggunakan PVA 3%. Karakterisasi dengan TEM menunjukkan nanopartikel perak yang disintesis berdasarkan rasio mol etilen glikol terhadap Ag+ 50:1 memiliki ukuran terkecil dengan kisaran 10,15–27,56 nm dengan struktur kristal face centered cubic (FCC. Semakin tinggi rasio mol EG /Ag+ dalam sintesis nanopartikel perak, semakin tinggi pula peningkatan absorbansinya.   Abstract __________________________________________________________________________________________ Silver nanoparticles are nanotechnology based product which can be applied as a catalyst and optic sensor detector. The factors that can effect on nanoparticle size are salt concentration and reductor agent. Silver nanoparticles are unstable material, so polyvinylalcohol needs to be added  as a stabilizer agent in their synthesis. The aims of this research are to

Study of the europium behavior in aqueous media

International Nuclear Information System (INIS)

Fernandez R, E.; Jimenez R, M.; Solache R, M.; Martinez M, V.

1999-01-01

Europium as waste can produce a pollution problem in water that is in contact with it, what would has a heavy environmental impacts, because of the possibilities of diffusion of these wastes from their place of confinement or storage until the geo and biosphere. The solution of such problem requires of a lot of knowledge over the behavior of several chemical elements such as europium in aqueous solutions. In this work it was used a low ion force (0.02 M). The data set will allow extrapolate the hydrolytic behavior of europium in too much minors ion force media, such as the ground waters, including in ion force zero

Smart surfaces with switchable superoleophilicity and superoleophobicity in aqueous media: Toward controllable oil/water separation

KAUST Repository

Zhang, L.; Zhang, Z.; Wang, Peng

2012-01-01

Advanced materials with surfaces that have controllable oil wettability when submerged in aqueous media have great potential for various underwater applications. Here we have developed smart surfaces on commonly used materials, including non

Photophysical and photoprototropic characteristics of phenothiazine in aqueous and β-cyclodextrin media

Energy Technology Data Exchange (ETDEWEB)

Rajamohan, Rajaram, E-mail: rajmohanau@gmail.com [Department of Chemistry, S.K.P Institute of Technology, Tiruvannamalai 606611 (India); Nayaki, Sundararajulu Kothai [Chemistry Section, FEAT, Annamalai University, Annamalainagar 608002 (India); Sivakumar, Krishnamoorthy [Department of Chemistry, SCSV University, Enathur, Kanchipuram 631561 (India); Swaminathan, Meenakshisundaram [Department of Chemistry, Annamalai University, Annamalainagar 608002 (India)

2015-12-15

The photophysical and photoprototropic characteristics of phenothiazine (PTZ) in aqueous and β-cyclodextrin (β-CD) media have been investigated using absorption, steady state and time resolved fluorescence measurements. The absorbance and fluorescence intensities of the neutral and monocationic forms of PTZ are enhanced by the addition of β-cyclodextrin and it is due to the formation of 1:1 inclusion complex. The formation of complex is confirmed by the decay analysis and Job's continuous variation method in the liquid state while FT-IR spectral study and SEM image analysis in the solid state. The peak and pK{sub a}* values of PTZ in aqueous media are higher than in β-CD medium, which reveals that the >NH group of PTZ lies in the β-CD cavity. - Highlights: • Increase in the absorbance and fluorescence intensity of PTZ by the addition of β-CDx is confirmed the complex formation. • Biexponential decay is noticed for PTZ by the addition of β-CDx is due to the formation of inclusion complex. • FT-IR and SEM images analysis confirms complex between PTZ and β-CDx in solid state. • The pK{sub a} and pK{sub a}* values of PTZ in aqueous medium is higher than in β-CDx medium, which reveals that the >NH group of PTZ lies in the β-CDx cavity. • The orientation of the inclusion complex is proposed by PatchDock server.

Enhanced Ga2O3-photocatalyzed and photochemical degradation of the Fipronil insecticide by UVC irradiation in mixed aqueous/organic media under an inert atmosphere.

Science.gov (United States)

Hidaka, Hisao; Tsukamoto, Tohru; Mitsutsuka, Yoshihiro; Oyama, Toshiyuki; Serpone, Nick

2015-05-01

Agrochemicals such as the insecticide Fipronil that bear fluoro groups are generally fat-soluble and nearly insoluble in water, so that their photodegradation in a heterogeneous aqueous gallium oxide dispersion presents some challenges. This article examined the photodegradation of this insecticide by solubilizing it through the addition of organic solvents (EtOH, MeOH, THF, 1,4-dioxane and ethylene glycol) to an aqueous medium and then subjecting the insecticide to 254 nm UVC radiation under photocatalytically inert (Ga2O3/N2) and air-equilibrated (Ga2O3/O2) conditions, as well as photochemically in the absence of Ga2O3 but also under inert and air-equilibrated conditions. Defluorination, dechlorination, desulfonation and denitridation of Fipronil were examined in mixed aqueous/organic media (10, 25 and 50 vol% in organic solvent). After 3 h of UVC irradiation (50 vol% mixed media) defluorination with Ga2O3/N2 was ∼65% greater than in aqueous media, and ca. 80% greater than the direct photolysis of Fipronil under inert (N2) conditions; under air-equilibrated conditions both Ga2O3-photocatalyzed and photochemical defluorination were significantly lower than in aqueous media. Dechlorination of Fipronil was ∼160% (Ga2O3/N2) and 140% (photochemically, N2) greater than in aqueous media; under air-equilibrated conditions, both photocatalyzed and photochemical formation of Cl(-) ions in mixed media fell rather short relative to aqueous media. The photocatalyzed (Ga2O3/N2) and photochemical (N2) conversion of the sulfur group in Fipronil to SO4(2(-)) ions was ca. 20% and 30% greater, respectively, in mixed media, while under air-equilibrated conditions photocatalyzed desulfonation was nearly twofold less than in the aqueous phase; direct photolysis showed little variations in mixed media. Denitridation of the nitrogens in Fipronil occurred mostly through the formation of ammonia (as NH4(+)) under all conditions with negligible quantities of NO3(-); again mixed media

Pengaruh Penambahan Aditif Bi2O3 Terhadap Karakteristik Barium Heksaferit Hasil Sintesis dengan Metode Sol-Gel

Directory of Open Access Journals (Sweden)

Siti Wardiyati Siswoyo

2017-11-01

Full Text Available Telah dilakukan sintesis barium heksaferit (BaFe12O19 secara sol-gel menggunakan prekursor barium nitrat [Ba(NO32], besi nitrat [Fe(NO33] dan asam sitrat (C6H8O7 Penelitian ini bertujuan untuk mendapatkan BaFe12O19 fasa tunggal berukuran nano dengan koersivitas magnetik tinggi. Untuk mencapai tujuan tersebut dilakukan penambahan aditif Bi2O3 dengan berbagai variasi persentase berat terhadap BaFe12O19 dari 0,5% sampai dengan 2%. Karakterisasi BaFe12O19 hasil sintesis dilakukan dengan  menggunakan alat X-ray diffraction (XRD untuk analisis  fasa, Fourier Transmission Infra Red (FTIR untuk mengetahui tipe ikatan yang terjadi, Scanning Electron Microscope dan Energy Dispersive X-ray Spectroscopy (SEM/EDS untuk analisis struktur dan persentase atom, dan Vibrating Sample Magnetometer VSM untuk mengetahui sifat magnetik yaitu koersivitas dan saturasi magnetik. Dari hasil percobaan diperoleh BaFe12O19 fasa tunggal dengan ukuran partikel sekitar 105 nm - 130 nm, saturasi magnetik 57,86 emu/g dan koersivitas magnetik sebesar 0,38 T. 

TiO2-based photocatalytic disinfection of microbes in aqueous media: A review.

Science.gov (United States)

Laxma Reddy, P Venkata; Kavitha, Beluri; Kumar Reddy, Police Anil; Kim, Ki-Hyun

2017-04-01

The TiO 2 based photocatalyst has great potential for the disinfection/inactivation of harmful pathogens (such as E.coli in aqueous media) along with its well-known usefulness on various chemical pollutants. The disinfection property of TiO 2 is primarily attributed to surface generation of reactive oxygen species (ROS) as well as free metal ions formation. Furthermore, its disinfection capacity and overall performance can be significantly improved through modifications of the TiO 2 material. In this review, we provide a brief survey on the effect of various TiO 2 materials in the disinfection of a wide range of environmentally harmful microbial pathogens (e.g., bacteria, fungi, algae, and viruses) in aqueous media. The influencing factors (such as reactor design, water chemistry, and TiO 2 modifications) of such processes are discussed along with the mechanisms of such disinfection. It is believed that the combined application of disinfection and decontamination will greatly enhance the utilization of TiO 2 photocatalyst as a potential alternative to conventional methods of water purification. Copyright © 2017 Elsevier Inc. All rights reserved.

Curcumin based optical sensing of fluoride in organo-aqueous media using irradiation technique

Science.gov (United States)

Venkataraj, Roopa; Radhakrishnan, P.; Kailasnath, M.

2017-06-01

The present work describes the degradation of natural dye Curcumin in organic-aqueous media upon irradiation by a multi-wavelength source of light like mercury lamp. The presence of anions in the solution leads to degradation of Curcumin and this degradation is especially enhanced in the case of fluoride ion. The degradation of Curcumin is investigated by studying the change in its absorption and fluorescence characteristics in organoaqueous solution upon irradiation. A broad detection range of fluoride ranging from 2.3×10-6-2.22×10-3 M points to the potential of the method of visible light irradiation enabling aqueous based sensing of fluoride using Curcumin.

Specific acid catalysis and Lewis acid catalysis of Diels–Alder reactions in aqueous media

NARCIS (Netherlands)

Mubofu, Egid B.; Engberts, Jan B.F.N.

2004-01-01

A comparative study of specific acid catalysis and Lewis acid catalysis of Diels–Alder reactions between dienophiles (1, 4 and 6) and cyclopentadiene (2) in water and mixed aqueous media is reported. The reactions were performed in water with copper(II) nitrate as the Lewis acid catalyst whereas

Specific acid catalysis and Lewis acid catalysis of Diels-Alder reactions in aqueous media

NARCIS (Netherlands)

Mubofu, E.B.; Engberts, J.B.F.N.

A comparative study of specific acid catalysis and Lewis acid catalysis of Diells-Alder reactions between dienophiles (1, 4 and 6) and cyclopentadiene (2) in water and mixed aqueous media is reported. The reactions were performed in water with copper(II) nitrate as the Lewis acid catalyst whereas

Polystyrene-Core, Silica-Shell Scintillant Nanoparticles for Low-Energy Radionuclide Quantification in Aqueous Media.

Science.gov (United States)

Janczak, Colleen M; Calderon, Isen A C; Mokhtari, Zeinab; Aspinwall, Craig A

2018-02-07

β-particle emitting radionuclides are useful molecular labels due to their abundance in biomolecules. Detection of β-emission from 3 H, 35 S, and 33 P, important biological isotopes, is challenging due to the low energies (E max ≤ 300 keV) and short penetration depths (≤0.6 mm) in aqueous media. The activity of biologically relevant β-emitters is usually measured in liquid scintillation cocktail (LSC), a mixture of energy-absorbing organic solvents, surfactants, and scintillant fluorophores, which places significant limitations on the ability to acquire time-resolved measurements directly in aqueous biological systems. As an alternative to LSC, we developed polystyrene-core, silica-shell nanoparticle scintillators (referred to as nanoSCINT) for quantification of low-energy β-particle emitting radionuclides directly in aqueous solutions. The polystyrene acts as an absorber for energy from emitted β-particles and can be loaded with a range of hydrophobic scintillant fluorophores, leading to photon emission at visible wavelengths. The silica shell serves as a hydrophilic shield for the polystyrene core, enabling dispersion in aqueous media and providing better compatibility with water-soluble analytes. While polymer and inorganic scintillating microparticles are commercially available, their large size and/or high density complicates effective dispersion throughout the sample volume. In this work, nanoSCINT nanoparticles were prepared and characterized. nanoSCINT responds to 3 H, 35 S, and 33 P directly in aqueous solutions, does not exhibit a change in scintillation response between pH 3.0 and 9.5 or with 100 mM NaCl, and can be recovered and reused for activity measurements in bulk aqueous samples, demonstrating the potential for reduced production of LSC waste and reduced total waste volume during radionuclide quantification. The limits of detection for 1 mg/mL nanoSCINT are 130 nCi/mL for 3 H, 8 nCi/mL for 35 S, and <1 nCi/mL for 33 P.

Synthesis of Co–Al layered double hydroxide nanoclusters as reduction nanocatalyst in aqueous media

Directory of Open Access Journals (Sweden)

Daisuke Kino

2017-12-01

Full Text Available Layered double hydroxides (LDHs have attracted attention as green materials due to their catalytic ability in benign aqueous solvents. We here demonstrate the synthesis of colloidal Co–Al LDH nanoclusters with an average size of <10 nm via a facile liquid-phase reaction for the enhancement of the catalytic activity. To the best of our knowledge, the present LDH is the smallest Co–Al LDH with an extremely large surface area and stability in an aqueous solvent, forming a stable and concentrated colloidal solution as high as 40 g/L. We investigated the formation mechanism, and the catalytic activity of Co–Al LDH nanoclusters. The Co–Al LDH nanoclusters showed 47 times higher rate of the reduction of dye molecules in the aqueous media than standard Co–Al LDH particles with a micrometer size. LDH nanoclusters demonstrated here are promising green nanocatalysts for the aqueous reaction processes.

Cation exchange properties of zeolites in hyper alkaline aqueous media.

Science.gov (United States)

Van Tendeloo, Leen; de Blochouse, Benny; Dom, Dirk; Vancluysen, Jacqueline; Snellings, Ruben; Martens, Johan A; Kirschhock, Christine E A; Maes, André; Breynaert, Eric

2015-02-03

Construction of multibarrier concrete based waste disposal sites and management of alkaline mine drainage water requires cation exchangers combining excellent sorption properties with a high stability and predictable performance in hyper alkaline media. Though highly selective organic cation exchange resins have been developed for most pollutants, they can serve as a growth medium for bacterial proliferation, impairing their long-term stability and introducing unpredictable parameters into the evolution of the system. Zeolites represent a family of inorganic cation exchangers, which naturally occur in hyper alkaline conditions and cannot serve as an electron donor or carbon source for microbial proliferation. Despite their successful application as industrial cation exchangers under near neutral conditions, their performance in hyper alkaline, saline water remains highly undocumented. Using Cs(+) as a benchmark element, this study aims to assess the long-term cation exchange performance of zeolites in concrete derived aqueous solutions. Comparison of their exchange properties in alkaline media with data obtained in near neutral solutions demonstrated that the cation exchange selectivity remains unaffected by the increased hydroxyl concentration; the cation exchange capacity did however show an unexpected increase in hyper alkaline media.

Mechanistic and kinetic aspects of pentose dehydration towards furfural in aqueous media employing homogeneous catalysis

NARCIS (Netherlands)

Danon, B.; Marcotullio, G.; De Jong, W.

2013-01-01

In this paper both the mechanistic and kinetic aspects of furfural formation from pentoses in aqueous acidic media have been reviewed. Based on the reviewed literature, a comprehensive reaction mechanism has been proposed consisting of more than one route, all starting from acyclic xylose, and

Removal of Ni (II), Co (II) and Pb (II) ions from aqueous media using ...

African Journals Online (AJOL)

Removal of Ni (II), Co (II) and Pb (II) ions from aqueous media using Starch ... The results showed that 0.025 % loaded SSMNPs gave the optimal sorption ... constants (Lagergren and Pseudo-2nd-order) for Ni2+ and Co2+ adsorption were ... Langmuir correlation coefficients showed a better fit for the adsorption isotherms.

Ultrasonic Assisted Synthesis of Chromenes Catalyzed by Sodium Carbonate in Aqueous Media.

Science.gov (United States)

Sabbaghan, Maryam; Sofalgar, Pegah

2015-01-01

A simple, efficient, and environmentally benign procedure for the synthesis of 2-amino-4H-chromene ring has been achieved by the three-component reaction of an aromatic aldehyde, malononitrile and diverse enolizable C-H activated compound under ultrasound irradiation using sodium carbonate as a catalyst in aqueous media. Sodium carbonate as a natural salt, being available as an inexpensive catalyst combined with ultrasound method promoted this protocol in comparison to other methods and catalysts.

Stripping of uranium from Dehpa/kerosene solvents by different aqueous media

International Nuclear Information System (INIS)

Khorfan, S.; Stas, J.; Kassem, M.

1998-01-01

Stripping uranium from Dehpa/kerosene solvent is a crucial step in the recovery of uranium. Stripping was studied using different stripping media mainly ammonium carbonate, phosphoric acid, sulfuric acid, hydrochloric acid and nitric acid. Stripping was measured at different operating conditions such as aqueous concentrations, temperatures, and Dehpa/kerosene concentrations. The results obtained showed that stripping by acid media increases with the acid concentration and follows the order: HF > H 3 PO 4 > H 2 SO 4 > HCl > HNO 3 . To achieve higher stripping by phosphoric acid it was found necessary to increase the temperature to 50 deg C, the acid concentration to 5 mol/l and to reduce the uranium to U 4+ . Stripping by basic media was found to increase with increasing concentration of the stripping media and to follow the order: Na 2 CO 3 > (NH 4 ) 2 CO 3 > NH 4 HCO 3 . Stripping by ammonium carbonate was found to increase with temperature and carbonate concentration. The stripping was optimized at 0.5 mol/l carbonate concentration and at a temperature of 50 deg C. Stripping was decreased by increasing concentration of Dehpa in kerosene and was depressed more by adding the synergant Topo to the Dehpa solvent especially at 1/4 mol/mol ratio. (author)

Towards water compatible MIPs for sensing in aqueous media.

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Horemans, F; Weustenraed, A; Spivak, D; Cleij, T J

2012-06-01

When synthesizing molecularly imprinted polymers (MIPs), a few fundamental principles should be kept in mind. There is a strong correlation between porogen polarity, MIP microenvironment polarity and the imprinting effect itself. The combination of these parameters eventually determines the overall binding behavior of a MIP in a given solvent. In addition, it is shown that MIP binding is strongly influenced by the polarity of the rebinding solvent. Because the use of MIPs in biomedical environments is of considerable interest, it is important that these MIPs perform well in aqueous media. In this article, various approaches are explored towards a water compatible MIP for the target molecule l-nicotine. To this end, the imprinting effect together with the MIP matrix polarity is fine-tuned during MIP synthesis. The binding behavior of the resulting MIPs is evaluated by performing batch rebinding experiments that makes it possible to select the most suitable MIP/non-imprinted polymer couple for future application in aqueous environments. One method to achieve improved compatibility with water is referred to as porogen tuning, in which porogens of varying polarities are used. It is demonstrated that, especially when multiple porogens are mixed, this approach can lead to superior performance in aqueous environments. Another method involves the incorporation of polar or non-polar comonomers in the MIP matrix. It is shown that by carefully selecting these monomers, it is also possible to obtain MIPs, which can selectively bind their target in water. Copyright © 2012 John Wiley & Sons, Ltd.

Effect of Aqueous Media on the Recovery of Scandium by Selective Precipitation

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Bengi Yagmurlu

2018-05-01

Full Text Available This research presents a novel precipitation method for scandium (Sc concentrate refining from bauxite residue leachates and the effect of aqueous media on this triple-stage successive precipitation process. The precipitation pattern and the precipitation behavior of the constituent elements was investigated using different precipitation agents in three major mineral acid media, namely, H2SO4, HNO3, and HCl in a comparative manner. Experimental investigations showed behavioral similarities between HNO3 and HCl media, while H2SO4 media was different from them because of the nature of the formed complexes. NH4OH was found to be the best precipitation agent in every leaching media to remove Fe(III with low Sc co-precipitation. To limit Sc loss from the system, Fe(III removal was divided into two steps, leading to more than 90% of Fe(III removal at the end of the process. Phosphate concentrates were produced in the final step of the precipitation process with dibasic phosphates which have a strong affinity towards Sc. Concentrates containing more than 50% of ScPO4 were produced in each case from the solutions after Fe(III removal, as described. A flow diagram of the selective precipitation process is proposed for these three mineral acid media with their characteristic parameters.

Pengaruh Advance Organizer Berbasis Proyek Terhadap Kemampuan Analisis – Sintesis Siswa

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Tasiwan -

2014-01-01

Full Text Available Penelitian ini dilakukan untuk mengetahui pengaruh model pengatur kemajuan (advance organizer berbasis proyek terhadap kemampuan analisis – sintesis siswa pada konsep Energi. Sebelum pembelajaran, diberikan tugas proyek pada siswa untuk merealisasikan bel listrik sederhana, rangkaian arus seri - paralel, dan tuas. Produk proyek digunakan sebagai advance organizer dalam pembelajaran di kelas. Penguatan kognitif dilakukan melalui diskusi kelompok dan pembuatan peta konsep, ekspositori guru di kelas, dan kegiatan eksperimen laboratorium. Data diambil melalui pretest, post test, observasi partisipatif pembelajaran oleh dua orang observer, penilaian produk, peta konsep dan laporan kegiatan eksperimen. Teknik analisis data meliputi uji prasyarat data dan uji hipotesis Hasil penelitian menunjukkan bahwa siswa mengalami peningkatan kemampuan analisis – sintesis dalam aspek menguraikan, mengkategorikan, mengidentifikasi, merumuskan pernyataan, merekonstruksi, menentukan konsep, dan menganalisis konsep dengan rata – rata peningkatan delta skor sebesar 54,46 %, uji t sebesar 6,4, dan skala gain sebesar 0,3. This study was conducted to determine the effect of project-based advance organizer model on student’s analysis - synthesis ability of the energy concept. Students were given an assignment to realize the project on simple electric bell, the series – parallel circuit, and lever, before learning. The products of project were used as an advanced organizer in the learning activity. Cognitive strengthening was done through group discussions and concept mapping, expository learning in the classroom, and laboratory experiments activities. The data were taken through a pretest, post-test, participant observation study by two observers, product assessment, concept maps and report of experiment activities. Results showed that the students’ analysis - synthesis ability increased in the aspect of describing, categorizing, identifying, statement

Lipase in biphasic alginate beads as a biocatalyst for esterification of butyric acid and butanol in aqueous media.

Science.gov (United States)

Ng, Choong Hey; Yang, Kun-Lin

2016-01-01

Esterification of organic acids and alcohols in aqueous media is very inefficient due to thermodynamic constraints. However, fermentation processes used to produce organic acids and alcohols are often conducted in aqueous media. To produce esters in aqueous media, biphasic alginate beads with immobilized lipase are developed for in situ esterification of butanol and butyric acid. The biphasic beads contain a solid matrix of calcium alginate and hexadecane together with 5 mg/mL of lipase as the biocatalyst. Hexadecane in the biphasic beads serves as an organic phase to facilitate the esterification reaction. Under optimized conditions, the beads are able to catalyze the production of 0.16 mmol of butyl butyrate from 0.5 mmol of butyric acid and 1.5 mmol of butanol. In contrast, when monophasic beads (without hexadecane) are used, only trace amount of butyl butyrate is produced. One main application of biphasic beads is in simultaneous fermentation and esterification (SFE) because the organic phase inside the beads is very stable and does not leach out into the culture medium. SFE is successfully conducted with an esterification yield of 6.32% using biphasic beads containing iso-octane even though the solvent is proven toxic to the butanol-producing Clostridium spp. Copyright © 2015 Elsevier Inc. All rights reserved.

Selective detection of Cu2 + and Co2 + in aqueous media: Asymmetric chemosensors, crystal structure and spectroscopic studies

Science.gov (United States)

Dogaheh, Samira Gholizadeh; Khanmohammadi, Hamid; Carolina Sañudo, E.

2017-05-01

Two new azo-azomethine receptors, H2L1 and H2L2, containing hydrazine, naphthalene and different electron withdrawing groups, Cl and NO2, have been designed and synthesized for qualitative and quantitative detection of Cu2 + and Co2 + in aqueous media. The crystal structure of H2L1is reported. The H2L1was used as a chemosensor for selective detection of trace amount of Cu2 + in aqueous media. H2L2 was also applied to naked-eye distinction of Cu2 + and Co2 + from other transition metal ions in aqueous media. Detection limit of Cu2 + is 1.13 μM and 1.26 μM, in water, for H2L1 and H2L2, respectively, which are lower than the World Health Organization (WHO) recommended level. The binuclear Cu2 + and Co2 + complexes of the receptors have been also prepared and characterized using spectroscopic methods and MALDI-TOF mass analysis. Furthermore, the binding stoichiometry between the receptors upon the addition Cu2 + and Co2 + has been investigated using Job's plot. Moreover, the fluorescence emission spectra of the receptors and their metal complexes are also reported.

Electrochemical behavior of meso-substituted iron porphyrins in alkaline aqueous media

Science.gov (United States)

Berezina, N. M.; Bazanov, M. I.; Maksimova, A. A.; Semeikin, A. S.

2017-12-01

The effect meso-substitution in iron porphyrin complexes has on their redox behavior in alkaline aqueous solutions is studied via cyclic voltammetry. The voltammetric features of the reduction of iron pyridylporphyrins suggest that the sites of electron transfer lie at the ligand, the metal ion, and the pyridyl moieties. The electron transfer reactions between the different forms of these compounds, including the oxygen reduction reaction they mediate, are outlined to show the sequence and potential ranges in which they occur in alkaline aqueous media. Under our experimental conditions, the iron porphyrins exist as μ-oxo dimmers whose activity for the electrocatalytic reduction of oxygen displays a considerable dependence on the nature of the substitutents and nitrogen isomerization (for pyridylporphyrins) and grows in the order (Fe( ms-Ph)4P)2O, (Fe[ ms-(Py-3)Ph3]P)2O, (Fe[ ms-(Py-4)4]P)2O, and (Fe[ ms-(Py-3)4]P)2O.

Mechanism of laser ablation for aqueous media irradiated under confined-stress conditions

International Nuclear Information System (INIS)

Oraevsky, A.A.; Jacques, S.L.; Tittel, F.K.

1995-01-01

Pulsed laser ablation of aqueous medium irradiated under conditions of temporal confinement of thermal stress is described. Time-resolved measurements of laser-induced transient stress waves with simultaneous imaging of ablation process by laser-flash photography were performed. Stress transients induced in aqueous solution of K 2 CrO 4 by ablative nanosecond laser pulses at 355 nm were studied by a broad-band lithium niobate acoustic transducer. Recoil momentum upon material ejection was measured from the temporal profiles of the acoustic transducer signal as a function of incident laser fluence. Cavitation bubbles produced in the irradiated volume during the tensile phase of thermoelastic stress were shown to drive material ejection at temperatures substantially below 100 degree C. Experimental data are evident that nanosecond-pulse laser ablation of aqueous media (when temporal stress-confinement conditions are satisfied) include the following two main stages of material ejection: (1) ejection of water microdroplets due to expansion and rupture of subsurface cavitation bubbles; (2) ejection of liquid streams with substantial volume upon collapse of initial crater and large cavitation bubbles in the depth of irradiated volume (after coalescence of smaller bubbles). copyright 1995 American Institute of Physics

Stripping of uranium from Dehpa/Kerosene solvents by different aqueous media

International Nuclear Information System (INIS)

Khorfan, S.; Stas, J.; Kassem, M.

2000-01-01

Stripping uranium from Dehpa/kerosene solvent is a crucial step in the recovery of uranium. Stripping was studied using different stripping media mainly ammonium carbonate, phosphoric acid, sulfuric acid, hydrochloric acid and nitric acid. Stripping was measured at different operating conditions such as aqueous concentrations, temperatures, and Dehpa/kerosene concentrations. The results obtained showed that stripping by acid media increases with the acid concentration and follows the order: HF > H sub 3 Po sub 4 > H sub 2 S O sub 4 > HCl > HNO sub 3. To achieve higher stripping by phosphoric acid it was found necessary to increase the temperature to 50 deg C, the acid concentration to 5 mol/l and to reduce the uranium to U sup 4 sup +. Stripping by basic media was found to increase with increasing concentration of the stripping media and to follow the order: Na sub 2 CO sub 3 > (NH sub 4) sub 2 CO sub 3 > NH sub 4 HCO sub 3. Stripping by ammonium carbonate was found to increase with temperature and carbonate concentration. The stripping was optimized at 0.5 mol/l carbonate concentration and at a temperature of 50 deg C. Stripping was decreased by increasing concentration of Dehpa in kerosene and was depressed more by adding the synergant TOPO to the Dehpa solvent especially at 1/4 mol/mol ratio. (author)

Layered Double Hydroxides as Effective Adsorbents for U(VI and Toxic Heavy Metals Removal from Aqueous Media

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G. N. Pshinko

2013-01-01

Full Text Available Capacities of different synthesized Zn,Al-hydrotalcite-like adsorbents, including the initial carbonate [Zn4Al2(OH12]·CO3·8H2O and its forms intercalated with chelating agents (ethylenediaminetetraacetic acid (EDTA, diethylenetriaminepentaacetic acid (DTPA, and hexamethylenediaminetetraacetic acid (HMDTA and heat-treated form Zn4Al2O7, to adsorb uranium(VI and ions of toxic heavy metals have been compared. Metal sorption capacities of hydrotalcite-like adsorbents have been shown to correlate with the stability of their complexes with the mentioned chelating agents in a solution. The synthesized layered double hydroxides (LDHs containing chelating agents in the interlayer space are rather efficient for sorption purification of aqueous media free from U(VI irrespective of its forms of natural abundance (including water-soluble bi- and tricarbonate forms and from heavy metal ions. [Zn4Al2(OH12]·EDTA·nH2O is recommended for practical application as one of the most efficient and inexpensive synthetic adsorbents designed for recovery of both cationic and particularly important anionic forms of U(VI and other heavy metals from aqueous media. Carbonate forms of LDHs turned out to be most efficient for recovery of Cu(II from aqueous media with pH0≥7 owing to precipitation of Cu(II basic carbonates and Cu(II hydroxides. Chromate ions are efficiently adsorbed from water only by calcinated forms of LDHs.

Extraction of lithium ion from alkaline aqueous media by a liquid surfactant membrane

International Nuclear Information System (INIS)

Kinugasa, Takumi; Ono, Yuri; Kawamura, Yuko; Watanabe, Kunio; Takeuchi, Hiroshi.

1995-01-01

Extraction of lithium ion from aqueous alkaline media by a liquid surfactant membrane was performed using a mixture of LIX54 and TOPO as the extractant. Stripping of lithium from the kerosene solution to the acid solution was suppressed with increasing content of polyamine (ECA) surfactant. The extraction rate of lithium by the liquid membrane could be interpreted taking account of an interfacial resistance due to ECA. It was confirmed that swelling of the (W/O) emulsion drops by water permeation through the liquid membrane is evaluated in terms of a change in osmotic pressure gradient between the external and internal aqueous phases during the lithium extraction. In the present operation, the extraction ratio of Li + from the external feed and the uptake into the internal phase reached as high as 95%. (author)

The effect of aqueous media on the mechanical properties of fluorapatite-mullite glass-ceramics.

Science.gov (United States)

Mollazadeh, S; Ajalli, Siamak; Kashi, Tahereh S Jafarzadeh; Yekta, Bijan Eftekhai; Javadpour, Jafar; Jafari, S; Youssefi, Abbas; Fazel, Akbar

2015-11-01

To verify the effects of alternating thermal changes in aqueous media and chemical composition on mechanical properties of apatite-mullite glass-ceramics and to investigate concentration of ions eluted from glass-ceramics in aqueous media. The glass compositions were from SiO2Al2O3P2O5CaOTiO2BaOZrO2CaF2 system. Glass-ceramics were prepared by heat-treating at 1100°C for 3h samples alternately immersed in water at 5 and 60°C. The 3-point bending strength (n=10) were determined using 3×4×25mm/bar and a universal testing machine, at a cross-head speed of 0.1mm/min. Vickers micro hardness were evaluated by applying a total of 15-20 indentations under a 100g load for 30s. Concentrations of ions eluted from glass-ceramics immersed in 60±5°C double distilled water were determined by ion chromatography. The toxicity of glass-ceramics was assessed by seeding the osteosarcoma cells (MG63) on powder for different days and their cell proliferation assessment was investigated by MTT assay. The data were analyzed using one way analysis of variance and the means were compared by Tukey's test (5% significance level). The highest flexural strength and hardness values after thermal changes belonged to TiO2 and ZrO2 containing glass-ceramics which contained lower amount of released ions. BaO containing glass-ceramic and sample with extra amount of silica showed the highest amount of reduction in their mechanical strength values. These additives enhanced the concentration of eluted ions in aqueous media. MTT results showed that glass-ceramics were almost equivalent concerning their in-vitro biological behavior. Thermal changes and chemical compositions had significant effects on flexural strength and Vickers micro-hardness values. Copyright © 2015 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

PREPARATION AND CHARACTERIZATION OF IRON THIN FILM ELECTRODEPOSED ON A VITREOUS CARBON ELECTRODE IN AQUEOUS AND ORGANIC MEDIA: A COMPARATIVE STUDY

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A LOUNAS

2010-06-01

studied on a vitreous carbon electrode in various aqueous and organic media. The deposit of iron was studied by cyclic voltammetry; the quantity of iron deposited was determined by integration of the cathodic and anodic peaks of Fe (0 and Fe (II of the various media.

Synthesis and characterization of ferrous phosphate (vivianite) and its behavior in aqueous media

International Nuclear Information System (INIS)

Diaz F, J.C.

2003-01-01

The synthesis and characterization of materials that can be useful in Environmental Chemistry is very important because their characteristics are exposed and its behavior in chemical phenomena as the sorption in aqueous media is understand to use it in the human being benefit. With the object of using, in a future, the octa hydrated ferrous phosphate (vivianite) as a potential candidate for matrix confinement in contention walls for the storage of radioactive waste of long half life, it was synthesized and it characterized physico chemically and their properties of surface of this compound were evaluated. Presently work was carried out the synthesis and structural characterization of the iron phosphate II by infrared spectroscopy with having Fourier transform, high vacuum scanning electron microscopy, X-ray diffraction, thermal gravimetric analysis, the BET multipoint surface area and Moessbauer spectroscopy; as well as, the determination between aqueous media of the isoelectric point and the density of sites of surface of the compound. The octa hydrated ferrous phosphate was obtained pure. The results indicate that the product corresponds to the prospective mineral, the vivianite. The thermal gravimetric analysis demonstrated that the ferrous phosphate is a stable salt after the lost of water. The isoelectric point is since an important parameter because allows to know the behavior of the surface of the material in aqueous systems, in this case the isoelectric point, of the octa hydrated ferrous phosphate, in distilled water is of pH 4.20 and in solution of potassium nitrate 0.5 M is of pH = 3.75. This indicates that the material has an amphoteric surface depending on the pH. On the other hand, the density of active sites of surface obtained by titrations acid-base is of 20 sites by nm 2 . (Author)

Basicity comparison for di-substituted 4-nitropyridine derivatives in polar non-aqueous media

International Nuclear Information System (INIS)

Gurzynski, Lukasz; Puszko, Aniela; Chmurzynski, Lech

2007-01-01

Acid dissociation, as well as cationic homoconjugation equilibria have been studied potentiometrically in systems involving four di-substituted 4-nitropyridines and conjugate cationic acids in the polar non-aqueous solvents - aprotic protophobic acetonitrile (AN) and propylene carbonate (PC), the amphiprotic methanol (MeOH), and in the aprotic protophilic dimethyl sulfoxide (DMSO). The influence of solvent effect on the obtained acidity constants has been discussed. The acidity constants (expressed as pK a values) were compared with those previously determined in another polar protophobic aprotic solvent - acetone (AC), and obtained for the unsubstituted pyridine (Py). A comparison of the acid dissociation constants determined in all media studied has proved that the strength of the cationic acids increases on going from acetonitrile through propylene carbonate, acetone, and methanol to dimethyl sulfoxide. Furthermore, the values of acidity constants in the non-aqueous media have shown that in all the solvents studied they change according to the substituent effects. It has been also found that substituted 4-nitropyridine derivatives studied exhibit no tendency towards cationic homoconjugation in acetonitrile, propylene carbonate, and methanol and dimethyl sulfoxide. Moreover, it has been demonstrated that the acid dissociation constants determined by potentiometric titration method in all the solutions investigated correlate well with the calculated energy parameters of the protonation reactions in the gaseous phase

Basicity comparison for di-substituted 4-nitropyridine derivatives in polar non-aqueous media

Energy Technology Data Exchange (ETDEWEB)

Gurzynski, Lukasz [Department of General and Inorganic Chemistry, University of Gdansk, Sobieskiego 18, 80-952 Gdansk (Poland); Puszko, Aniela [Department of Organic Chemistry, School of Economics, Wroclaw (Poland); Chmurzynski, Lech [Department of General and Inorganic Chemistry, University of Gdansk, Sobieskiego 18, 80-952 Gdansk (Poland)], E-mail: lech@chemik.chem.univ.gda.pl

2007-12-15

Acid dissociation, as well as cationic homoconjugation equilibria have been studied potentiometrically in systems involving four di-substituted 4-nitropyridines and conjugate cationic acids in the polar non-aqueous solvents - aprotic protophobic acetonitrile (AN) and propylene carbonate (PC), the amphiprotic methanol (MeOH), and in the aprotic protophilic dimethyl sulfoxide (DMSO). The influence of solvent effect on the obtained acidity constants has been discussed. The acidity constants (expressed as pK{sub a} values) were compared with those previously determined in another polar protophobic aprotic solvent - acetone (AC), and obtained for the unsubstituted pyridine (Py). A comparison of the acid dissociation constants determined in all media studied has proved that the strength of the cationic acids increases on going from acetonitrile through propylene carbonate, acetone, and methanol to dimethyl sulfoxide. Furthermore, the values of acidity constants in the non-aqueous media have shown that in all the solvents studied they change according to the substituent effects. It has been also found that substituted 4-nitropyridine derivatives studied exhibit no tendency towards cationic homoconjugation in acetonitrile, propylene carbonate, and methanol and dimethyl sulfoxide. Moreover, it has been demonstrated that the acid dissociation constants determined by potentiometric titration method in all the solutions investigated correlate well with the calculated energy parameters of the protonation reactions in the gaseous phase.

Some aspects of synergistic extraction of actinides and lanthanides from mixed aqueous-organic media

International Nuclear Information System (INIS)

Shukla, J.P.; Subramanian, M.S.

1981-01-01

Various aspects of the synergistic extraction and separation of actinides and lanthanides from mixed aqueous-organic solutions (polar media) have been reviewed. Notable recent developments as well as its current status in solvent extraction systems where the aqueous acidic phase contains an organic solvent which is completely miscible with water, are presented briefly. In general, extraction increases in the presence of an organic component. The less polar the additive, the higher is the tendency to form neutral metal complexes which ultimately brings about an increase in the extraction. In a polar media, synergism has mostly been observed, though antagonism is not uncommon. An attempt has been made to classify the factors that play an important role in polar phase extractions. Also, their influence particularly on the extractability of actinides and lanthanides is discussed. The discussion is limited to the factors affecting the extraction equilibria, effect of dielectric constant of the polar medium, solvation of the extracting agent and to the composition and stability of the metal complex in the organic phase. Hydroxyl (OHsup(-)) bearing organic additives, e.g. alcohols, and solvents not containing the hydroxyl group such as acetone, dimethylsulphoxide, tetrahydrofuran, amides and acetonitrile etc. are the two major classes of organic additives considered in these studies. Generally, synergistic effect in extraction of the ion-association (TBP, TOPO, sulphoxides etc.) or anion exchange (amines etc.) type is relatively more pronounced compared to other extractions. A tabular summary concerning extraction of actinides and lanthanides from polar media is appended for ready reference. (author)

SINTESIS SILIKA AEROGEL DENGAN BAHAN DASAR ABU BAGASSE

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Nazriati Nazriati

2012-05-01

Full Text Available SYNTHESIS OF SILICA AEROGEL FROM BAGASSE ASH. Synthesis of silica aerogel from bagasse ash was done by alkaline extraction followed by sol-gel. Bagasse ash was extracted with NaOH at its boiling temperature for one hour with continue stirring, to produce sodium silicate. Subsequently, sodium silicate was pass through ionic exchanger resin, to produces silicic acid (SA. Silicic acid solution was then added with TMCS and HMDS as surface modifier agent. In order to form gel pH must be adjusted to final pH of 8-9 by addition of NH4OH solution. The resulting gel then was aged and dried at ambient pressure and at a certain time and temperature. Characterization of products was done by measuring its pore volume, surface area, and hydrophobisity (contact angle. TMCS serves as water expeller from the pores and subsequently surface was modified by HMDS and TMCS. HMDS content will linearly increase surface area, pore volume, and the contact angle of the resulting silica aerogel. Characteristics of silica aerogel was generated by varying the composition of the SA:TMCS:HMDS resulting has a surface area of 50-488 m2/g, pore volume from 0.2 to 0.9 m3 /g, the contact angle of 48-119 and pore diameter ranging from 5.7-22.56 nm. Based on the resulting pore diameter, the synthesized of silica aerogel categorized as mesoporous.      Abstrak   Sintesis silika aerogel dari bahan dasar abu bagasse dilakukan dengan ekstraksi basa dan diikuti dengan sol-gel. Abu bagasse diekstrak dengan NaOH pada suhu didihnya sambil diaduk selama satu jam, menghasilkan sodium silikat. Selanjutnya, sodium silikat dilewatkan resin penukar ion, menghasilkan asam silicic (SA. Larutan asam silicic kemudian ditambahkan trimethy­l­chlorosilane (TMCS dan hexamethyldisilazane (HMDS sebagai agen pemodifikasi permukaan. Untuk terjadinya gel pH diatur hingga mencapai 8-9 dengan penambahan larutan NH4OH. Gel yang dihasilkan kemudian di-aging dan dikeringkan pada tekanan ambien pada suhu dan

Radiation-induced changes of liposomes and lecithin in non-aqueous media

International Nuclear Information System (INIS)

Nakazawa, T.; Nagatsuka, S.; Sakurai, T.

1981-01-01

Radiation-induced changes of lipids in non-aqueous media were studied to elucidate the process of radiation damage in biological membranes. The lipid peroxidation progressed linearly with increasing dose and decreasing dose rate of γ-irradiation in soyabean lecithin in chloroform. The fatty acid composition of lecithin also changed, especially in linoleic and linolenic acids. Lower dose rate radiation enhanced these changes in oxic condition. Lipid peroxidation was also shown in lipids extracted from irradiated liposomes or in liposomes prepared from irradiated lecithin in chloroform. The dose-dependent glucose efflux was seen in liposomes prepared from irradiated lecithin in chloroform. These results indicate that the peroxidation of lipid molecules might cause radiation damage to the membrane conformation. (author)

The use of biosorbents for heavy metals removal from aqueous media

International Nuclear Information System (INIS)

Al-Masri, M. S.; Amin, Y.

2010-04-01

Biomaterials, which could be adsorbed heavy metals, such bacteria, algae, yeasts, fungi and agricultural waste, is called Biomass. Recently, they are widely used for heavy metal removal from aqueous media, due to their large available quantities, low cost and good performance. The biosorbent, unlike mono functional ion exchange resins, contains variety of functional sites including carboxyl, imidazole, sulphydryl, amino, phosphate, sulfate, thioether, phenol, carbonyl, amide and hydroxyl moieties. In this paper, the biosorbents word widely and nationally used for heavy metal removal were reviewed. Their biosorption performance, their pretreatment and modification, aiming to improve their sorption capacity, and regeneration/reuse was introduced and evaluated. The potential application of biosorption and biosorbents was discussed. (author)

Deep Eutectic Solvent Aqueous Solutions as Efficient Media for the Solubilization of Hardwood Xylans.

Science.gov (United States)

Morais, Eduarda S; Mendonça, Patrícia V; Coelho, Jorge F J; Freire, Mara G; Freire, Carmen S R; Coutinho, João A P; Silvestre, Armando J D

2018-02-22

This work contributes to the development of integrated lignocellulosic-based biorefineries by the pioneering exploitation of hardwood xylans by solubilization and extraction in deep eutectic solvents (DES). DES formed by choline chloride and urea or acetic acid were initially evaluated as solvents for commercial xylan as a model compound. The effects of temperature, molar ratio, and concentration of the DES aqueous solutions were evaluated and optimized by using a response surface methodology. The results obtained demonstrated the potential of these solvents, with 328.23 g L -1 of xylan solubilization using 66.7 wt % DES in water at 80 °C. Furthermore, xylans could be recovered by precipitation from the DES aqueous media in yields above 90 %. The detailed characterization of the xylans recovered after solubilization in aqueous DES demonstrated that 4-O-methyl groups were eliminated from the 4-O-methylglucuronic acids moieties and uronic acids (15 %) were cleaved from the xylan backbone during this process. The similar M w values of both pristine and recovered xylans confirmed the success of the reported procedure. DES recovery in four additional extraction cycles was also demonstrated. Finally, the successful extraction of xylans from Eucalyptus globulus wood by using aqueous solutions of DES was demonstrated. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

XAS Investigation of bio-relevant cobalt complexes in aqueous media

International Nuclear Information System (INIS)

Bresson, C.; Lamouroux, C.; Esnouf, S.; Solari, P.L.; Den Auwer, C.

2006-01-01

Cobalt is an essential element of biological cycles involved in numerous metallo-biomolecules, but it becomes a toxic element at high concentration or a radio-toxic element because of its use in the nuclear industry. 'Molecular speciation' in biological media is an essential prerequisite to evaluate its chemical behaviour as well as its toxic or beneficial effects. In this scheme, we have focused on the coordination properties of the thiol-containing amino acid cysteine (Cys) and the pseudo-peptide N-(2-mercapto-propionyl) glycine (MPG) towards the Co 2+ cation in aqueous media. XAS at the Co K edge and traditional spectroscopic techniques have been coupled in order to structurally characterize the cobalt coordination sphere. Oxidation states and geometries of the bis- and tris-cysteinato Co(III) complexes are in agreement with the literature data. In addition, bond lengths between the metallic centre and the donor atoms have been determined. The structure of a new dimeric N-(2-mercapto-propionyl) glycinato Co(II) complex in solution is also reported. The coordination of MPG to Co(II) through the thiolate and carboxylate functions is ascertained. This work provides fundamental structural information about bio-relevant complexes of cobalt, which will contribute to our understanding of the chemical behaviour and the biological role of this radionuclide. (authors)

Spectroscopic and redox properties of curium and californium ions in concentrated aqueous carbonate-bicarbonate media

International Nuclear Information System (INIS)

Hobart, D.E.; Varlashkin, P.G.; Samhoun, K.; Haire, R.G.; Peterson, J.R.

1983-01-01

Multimilligram quantities of trivalent curium-248 and californium-249 were investigated by absorption spectroscopy, cyclic voltammetry, and bulk solution electrolysis in concentrated aqueous carbonate-bicarbonate solution. Actinide concentrations between 10 -4 and 10 -2 M were studied in 2 M sodium carbonate and 5.5 M potassium carbonate solutions at pH values from 8 to 14. The solution absorption spectra of Cm(III) and Cf(III) in carbonate media are presented for the first time and compared to literature spectra of these species in noncomplexing aqueous solution. It was anticipated that carbonate complexation of the actinide ions could provide a sufficient negative shift in the formal potentials of the M(IV)/M(III) couples of Cm and Cf to permit the generation and stabilization of their tetravalent states in aqueous carbonate-bicarbonate medium. No conclusive evidence was found in the present work to indicate the existence of any higher oxidation states of curium or californium in carbonate solution. Some possible reasons for our inability to generate and detect oxidized species of curium and californium in this medium are discussed

Recovery of homogeneous polyoxometallate catalysts from aqueous and organic media by a mesoporous ceramic membrane without loss of catalytic activity.

Science.gov (United States)

Roy Chowdhury, Sankhanilay; Witte, Peter T; Blank, Dave H A; Alsters, Paul L; Ten Elshof, Johan E

2006-04-03

The recovery of homogeneous polyoxometallate (POM) oxidation catalysts from aqueous and non-aqueous media by a nanofiltration process using mesoporous gamma-alumina membranes is reported. The recovery of Q(12)[WZn(3)(ZnW(9)O(34))(2)] (Q=[MeN(n-C(8)H(17))(3)](+)) from toluene-based media was quantitative within experimental error, while up to 97 % of Na(12)[WZn(3)(ZnW(9)O(34))(2)] could be recovered from water. The toluene-soluble POM catalyst was used repeatedly in the conversion of cyclooctene to cyclooctene oxide and separated from the product mixture after each reaction. The catalytic activity increased steadily with the number of times that the catalyst had been recycled, which was attributed to partial removal of the excess QCl that is known to have a negative influence on the catalytic activity. Differences in the permeability of the membrane for different liquid media can be attributed to viscosity differences and/or capillary condensation effects. The influence of membrane pore radius on permeability and recovery is discussed.

Influence of enzymes on the oil extraction processes in aqueous media

Directory of Open Access Journals (Sweden)

Ricochon Guillaume

2010-11-01

Full Text Available The methods of oil aqueous extraction process (AEP assisted by enzymes are, over the last 50 years, an alternative designed to replace traditional methods of extraction using organic solvents. To extract the oil using an AEP, the use of specific enzymes, able to hydrolyze some or all components of seeds, can significantly increase the yields of extraction. Hydrolyzing the different constituents of cell walls (cellulose, hemicellulose, pectins, proteins, etc., enzymes are able to enhance the liberation of the oil. A number of physico-chemical parameters must also be considered for the better expression of the enzymatic mixture, while maintaining the quality of oils and meals. This article presents the various factors influencing the release of oil in aqueous media and the main results obtained by this process on various substrates.

BANGUNAN TINGGI MULTI FUNGSI SEBAGAI SINTESIS ARSITEKTUR DAN STRUKTUR Studi Analisis Jin Mao Tower Grand Hyatt Shanghai

Directory of Open Access Journals (Sweden)

Jimmy Priatman

2005-01-01

Full Text Available More than two decades, after the emerging of post- modern architecture, the split between construction technology and cultural expression in architecture appeared to become wider and wider. With the exception of a few "high-tech" buildings, the unity of art and applied science (technology in design seems facing challenges. It is interesting to see how fast and unexpectedly the situation has changed. Many factors and people played a role in this reversal, many new buildings demonstrate that utilitarian artifacts do not have to be oppressive to creativity but can evoke new innovation. One of the most significant contributors was JIN MAO TOWER at Shanghai, China. The paper analyses this building as a genuine synthesis of rational intelligence with art poetry that is still possible. Abstract in Bahasa Indonesia : Lebih dari dua dekade setelah timbulnya arsitektur pasca modern, pemisahan antara tekknologi konstruksi dan ekspresi kultural dalam arsitektur menjadi semakin lebar. Dengan perkecualian beberapa gedung "high-tech", kesatuan antara seni dan teknologi dalam tahap desain terlihat menghadapi tantangan tantangan. Tetapi menarik untuk diamati bahwa situasi telah berubah. Banyak faktor dan tokoh tokoh arsitek memegang peranan penting dalam perubahan ini, banyak bangunan bangunan baru mendemontrasikan bahwa artefak fungsionil tidak bearti menindas kreativitas namun dapat membangkitkan inovasi baru. Salah satu kontributor yang sangat penting adalah JIN MAO TOWER di Shanghai-China. Makalah ini membahas bangunan tersebut sebagai sintesis orijinal yang masih memungkinkan antara kecerdasan rasional dengan puisi seni arsitektur. Kata kunci: Sintesis.

Desalination of aqueous media using ionic liquids

NARCIS (Netherlands)

2014-01-01

The present invention relates to a method for extracting metal and/or metalloid ions from an aqueous medium, comprising the steps of: a) mixing the aqueous medium with an ionic liquid comprising an aliphatic carboxylate anion having at least one unsaturated carbon-carbon bond, or and/or with a

TiO{sub 2}-based photocatalytic disinfection of microbes in aqueous media: A review

Energy Technology Data Exchange (ETDEWEB)

Laxma Reddy, P.Venkata [Program in Environmental Science and Engineering, University of Texas El Paso, El Paso, TX 799038 (United States); Kavitha, Beluri [Department of Pharmacology, Kamineni Institute of Medical Sciences, Dr. NTRUHS, Vijayawada, Andhra Pradesh 520008 (India); Kumar Reddy, Police Anil [School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 38541 (Korea, Republic of); Kim, Ki-Hyun, E-mail: kkim61@hanyang.ac.kr [Department of Civil & Environmental Engineering, Hanyang University, 222 Wangsimni-Ro, Seoul 04763 (Korea, Republic of)

2017-04-15

The TiO{sub 2} based photocatalyst has great potential for the disinfection/inactivation of harmful pathogens (such as E.coli in aqueous media) along with its well-known usefulness on various chemical pollutants. The disinfection property of TiO{sub 2} is primarily attributed to surface generation of reactive oxygen species (ROS) as well as free metal ions formation. Furthermore, its disinfection capacity and overall performance can be significantly improved through modifications of the TiO{sub 2} material. In this review, we provide a brief survey on the effect of various TiO{sub 2} materials in the disinfection of a wide range of environmentally harmful microbial pathogens (e.g., bacteria, fungi, algae, and viruses) in aqueous media. The influencing factors (such as reactor design, water chemistry, and TiO{sub 2} modifications) of such processes are discussed along with the mechanisms of such disinfection. It is believed that the combined application of disinfection and decontamination will greatly enhance the utilization of TiO{sub 2} photocatalyst as a potential alternative to conventional methods of water purification. - Highlights: • The advent of industrialization jeopardized the quality of drinking water. • TiO{sub 2} photocatalysis holds promise both in the degradation of pollutants and for disinfection. • The applicability of TiO{sub 2}-based decontamination is explored for microbial disinfection. • Here we provide a comprehensive review on titania-based photocatalysts for disinfection.

Detection of biologically important anions in aqueous media by dicationic azaborines bearing ammonio or phosphonio groups.

Science.gov (United States)

Agou, Tomohiro; Sekine, Masaki; Kobayashi, Junji; Kawashima, Takayuki

2009-01-01

New cationic triarylboranes bearing ammonio or phosphonio groups on the periphery were synthesized from a common intermediate, a dibromodibenzoazaborine. These cationic molecules are soluble in highly polar organic solvents as well as water, and they exhibit strong light absorption and photoluminescence emission in water. Complexation of the cationic azaborines with fluoride and cyanide ions in aqueous media proceeded and could be monitored by NMR, UV/Vis, and fluorescence spectroscopy.

Reactive transport of aqueous protons in porous media

KAUST Repository

McNeece, Colin J.

2016-10-09

The sorption of protons determines the surface charge of natural media and is therefore a first-order control on contaminant transport. Significant effort has been extended to develop chemical models that quantify the sorption of protons at the mineral surface. To compare these models’ effect on predicted proton transport, we present analytic solutions for column experiments through silica sand. Reaction front morphology is controlled by the functional relationship between the total sorbed and total aqueous proton concentrations. An inflection point in this function near neutral pH leads to a reversal in the classic front formation mechanism under basic conditions, such that proton desorption leads to a self-sharpening front, while adsorption leads to a spreading front. A composite reaction front comprising both a spreading and self-sharpening segment can occur when the injected and initial concentrations straddle the inflection point. This behavior is unique in single component reactive transport and arises due to the auto-ionization of water rather than electrostatic interactions at the mineral surface. We derive a regime diagram illustrating conditions under which different fronts occur, highlighting areas where model predictions diverge. Chemical models are then compared and validated against a systematic set of column experiments.

Suzuki-Miyaura cross-coupling reactions in aqueous media: green and sustainable syntheses of biaryls.

Science.gov (United States)

Polshettiwar, Vivek; Decottignies, Audrey; Len, Christophe; Fihri, Aziz

2010-05-25

Carbon-carbon cross-coupling reactions are among the most important processes in organic chemistry, and Suzuki-Miyaura reactions are among the most widely used protocols for the formation of carbon-carbon bonds. These reactions are generally catalyzed by soluble palladium complexes with various ligands. However, the use of toxic organic solvents remains a scientific challenge and an aspect of economical and ecological relevance. This Review will summarize various recently developed significant methods by which the Suzuki-Miyaura coupling was conducted in aqueous media, and analyzes if they are "real green" protocols.

Solvation thermodynamics of L-cystine, L-tyrosine, and L-leucine in aqueous-electrolyte media

Science.gov (United States)

Roy, Sanjay; Guin, Partha Sarathi; Mahali, Kalachand; Dolui, Bijoy Krishna

2017-12-01

Solubilities of L-cystine, L-tyrosine, and L-leucine in aqueous NaCl media at 298.15 K have been studied. Indispensable and related solvent parameters such as molar mass, molar volume, etc., were also determined. The results are used to evaluate the standard transfer Gibbs free energy, cavity forming enthalpy of transfer, cavity forming transfer Gibbs free energy and dipole-dipole interaction effects during the course of solvation. Various weak interactions involving solute-solvent or solvent-solvent molecules were characterized in order to find their role on the solvation of these amino acids.

Pitting morphologies of zirconium base alloys in aqueous and non aqueous chloride media

International Nuclear Information System (INIS)

Palit, G.C.; Gadiyar, H.S.

1988-01-01

Pitting morphology of zirconium and Zr-Cr alloys in aqueous chloride and nonaqueous methanol + 0.4 per cent HCl solution was investigated and observed to follow different modes in these two environments. While in aqueous chloride solution pitting was transgranular and randomly oriented, in methanol-chloride solution pits were observed to initiate and propagate along the grain boundaries. In aqueous chloride solution very irregular and sponge like zirconium metal was formed inside the pit while in methanol-chloride solution the pits were crystallographic in nature. Optical microscopy has revealed that pits preferentially initiate and propagate along scratch line in aqueous chloride solution, but such was not the case in nonaqueous methanol-chloride solution. The nature and the mechanism operating in the catastropic failure of these materials are investigated. (author). 10 refs., 11 figs

Mass spectrometric detection of proteins in non-aqueous media : the case of prion proteins in biodiesel

Energy Technology Data Exchange (ETDEWEB)

Douma, M.D.; Kerr, G.M.; Brown, R.S.; Keller, B.O.; Oleschuk, R.D. [Queen' s Univ., Kingston, ON (Canada). Dept. of Chemistry

2008-08-15

This paper presented a filtration method for detecting protein traces in non-aqueous media. The extraction technique used a mixture of acetonitrile, non-ionic detergent and water along with filter disks with embedded C{sub 8}-modified silica particles to capture the proteins from non-aqueous samples. The extraction process was then followed by an elution of the protein from the filter disk and direct mass spectrometric detection and tryptic digestion with peptide mapping and MS/MS fragmentation of protein-specific peptides. The method was used to detect prion proteins in spiked biodiesel samples. A tryptic peptide with the sequence YGQGSPGGNR was used for unambiguous identification. Results of the study showed that the method is suitable for the large-scale testing of protein impurities in tallow-based biodiesel production processes. 33 refs., 6 figs.

One-pot synthesis of Fe3O4@Chitosan-pSDCalix hybrid nanomaterial for the detection and removal of Hg2+ ion from aqueous media

Science.gov (United States)

Bhatti, Asif Ali; Oguz, Mehmet; Yilmaz, Mustafa

2018-03-01

New one pot mesoporous hybrid material containing iron nanoparticles fabricated with chitosan and p-sulfonato dansyl calix[4]arene composite (Fe3O4@Chitosan-pSDCalix) has been susccessfully synthesized. These mesoporous fluorescence iron nanoparticles were applied for the detection and removal of environmentally toxic Hg2+ ion from aqueous media. Different techniques were applied to confirm the preparation of Fe3O4@Chitosan-pSDCalix such as HRTEM, TGA/DTA, FTIR and XRD. Synthesized nanoparticles have average size of 17 nm with pore size of 0.19 nm as revealed from HRTEM images. Fluorescence study follow the photoinduced electron transfer process after addition of Hg2+ in the solution with decrease in intensity. Confocal microscope images were also acquired to confirm the presence of Hg2+ on nanoparticles. Adsorption study suggests that the removal of Hg2+ from aqueous media follows Langmuir adsorption isotherm. These studies suggest the synthesized Fe3O4@Chitosan-pSDCalix is an efficient hybrid material for the detection and removal of Hg2+ ion from aqueous media, and that it can also be used in biomolecules for the detection of toxic metal ions.

Suzuki-Miyaura cross-coupling reactions in aqueous media: Green and sustainable syntheses of biaryls

KAUST Repository

Polshettiwar, Vivek

2010-02-28

Carbon-carbon cross-coupling reactions are among the most important processes in organic chemistry, and Suzuki-Miyaura reactions are among the most widely used protocols for the formation of carbon-carbon bonds. These reactions are generally catalyzed by soluble palladium complexes with various ligands. However, the use of toxic organic solvents remains a scientific challenge and an aspect of economical and ecological relevance. This Review will summarize various recently developed significant methods by which the Suzuki-Miyaura coupling was conducted in aqueous media, and analyzes if they are "real green" protocols. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Mixed system of ionic liquid and non-ionic surfactants in aqueous media: Surface and thermodynamic properties

International Nuclear Information System (INIS)

Bhatt, Darshak; Maheria, Kalpana; Parikh, Jigisha

2014-01-01

Highlights: • Interaction of ionic liquid and ethylene oxide based non-ionic surfactants in aqueous media. • Evaluation of various surface properties and thermodynamic parameters. • Micellar growth ensues from exothermic to endothermic with increase in temperature. • Micelle formation is enthalpy driven at low temperature and entropy driven at higher temperature. • The micellization power and adsorption proficiency decreased at high IL concentrations. - Abstract: The mixed system of ionic liquid (IL) tetraethyl ammonium tetrafluoroborate [TEA(BF 4 )] and numerous ethylene oxide based non-ionic surfactants in aqueous media were studied using surface tension, viscosity and dynamic light scattering (DLS) measurements. Various surface properties like critical micelle concentration (cmc), maximum surface excess concentration (Γ max ), minimum surface area per surfactant molecule (A min ), surface tension at the cmc (γ cmc ), adsorption efficiency (pC 20 ), and effectiveness of surface tension reduction (π cmc ) as well as thermodynamic parameters of micellization have been determined. DLS and viscosity measurements revealed that the micellar growth was attributed to the bridged solvophilicity of the POE chain in surfactants at elevated temperatures. In most of the cases, the progression ensues from exothermic to endothermic with increase in temperature of the mixed system. Thermodynamic parameter indicates that the micelle formation process is enthalpy driven at low temperature and entropy driven at higher temperature

A nanofiber functionalized with dithizone by co-electrospinning for lead (II) adsorption from aqueous media

International Nuclear Information System (INIS)

Deng, Jianjun; Kang, Xuejun; Chen, Liqin; Wang, Yu; Gu, Zhongze; Lu, Zuhong

2011-01-01

Highlights: ► We fabricated a composite electrospun nanofiber as a selective sorbent for lead (II) in PFSPE. ► The composite nanofiber was functionalized with the dithizone by co-electrospinning of the PS solution containing unbonded dithizone. ► The nanofiber was characterized by scanning electron microscope and IR spectra. ► We applied the nanofiber by packing in a cartridge. ► The nanofiber performed well in the absorption of lead (II) and was applied successfully in aqueous samples. - Abstract: An electrospun nanofiber was utilized as a sorbent in packed fiber solid phase extraction (PFSPE) for selective separation and preconcentration of lead (II). The nanofiber had a polystyrene (PS) backbone, which was functionalized with dithizone (DZ) by co-electrospinning of a PS solution containing DZ. The nanofiber exhibited its performance in a cartridge prepared by packing 5 mg of nanofiber. The nanofiber was characterized by a scanning electron microscope and IR spectra. The diameter of the nanofiber was less than 400 nm. After being activated by 2.0 mol L −1 NaOH aqueous solution, the nanofiber quantitatively sorbed lead (II) at pH 8.5, and the metal ion could be desorbed from it by three times of elution with a small volume of 0.1 mol L −1 HNO 3 aqueous solution. The breakthrough capacity was 16 μg mg −1 . The nanofiber could be used for concentration of lead (II) from water and other aqueous media, such as plasma with stable recovery in a simple and convenient manner.

A rapid method to estimate uranium using ionic liquid as extracting agent from basic aqueous media

International Nuclear Information System (INIS)

Prabhath Ravi, K.; Sathyapriya, R.S.; Rao, D.D.; Ghosh, S.K.

2016-01-01

Room temperature ionic liquids, as their name suggests are salts with a low melting point typically less than 100 °C and exist as liquid at room temperature. The common cationic parts of ionic liquids are imidazolium, pyridinium, pyrrolidinium, quaternary ammonium, or phosphonium ions, and common anionic parts are chloride, bromide, boron tetrafluorate, phosphorous hexafluorate, triflimide etc. The physical properties of ionic liquids can be tuned by choosing appropriate cations with differing alkyl chain lengths and anions. Application of ionic liquids in organic synthesis, liquid-liquid extractions, electrochemistry, catalysis, speciation studies, nuclear reprocessing is being studied extensively in recent times. In this paper a rapid method to estimate the uranium content in aqueous media by extraction with room temperature ionic liquid tricaprylammoniumthiosalicylate ((A- 336)(TS)) followed by liquid scintillation analysis is described. Re-extraction of uranium from ionic liquid phase to aqueous phase was also studied

Dispersion of Nanomaterials in Aqueous Media: Towards Protocol Optimization.

Science.gov (United States)

Kaur, Inder; Ellis, Laura-Jayne; Romer, Isabella; Tantra, Ratna; Carriere, Marie; Allard, Soline; Mayne-L'Hermite, Martine; Minelli, Caterina; Unger, Wolfgang; Potthoff, Annegret; Rades, Steffi; Valsami-Jones, Eugenia

2017-12-25

The sonication process is commonly used for de-agglomerating and dispersing nanomaterials in aqueous based media, necessary to improve homogeneity and stability of the suspension. In this study, a systematic step-wise approach is carried out to identify optimal sonication conditions in order to achieve a stable dispersion. This approach has been adopted and shown to be suitable for several nanomaterials (cerium oxide, zinc oxide, and carbon nanotubes) dispersed in deionized (DI) water. However, with any change in either the nanomaterial type or dispersing medium, there needs to be optimization of the basic protocol by adjusting various factors such as sonication time, power, and sonicator type as well as temperature rise during the process. The approach records the dispersion process in detail. This is necessary to identify the time points as well as other above-mentioned conditions during the sonication process in which there may be undesirable changes, such as damage to the particle surface thus affecting surface properties. Our goal is to offer a harmonized approach that can control the quality of the final, produced dispersion. Such a guideline is instrumental in ensuring dispersion quality repeatability in the nanoscience community, particularly in the field of nanotoxicology.

Thermal MEMS actuator operation in aqueous media/seawater: Performance enhancement through atomic layer deposition post processing of PolyMUMPs devices

Energy Technology Data Exchange (ETDEWEB)

Warnat, Stephan, E-mail: stephan.warnat@dal.ca; Forbrigger, Cameron; Hubbard, Ted [Mechanical Engineering, Dalhousie University, Halifax, Nova Scotia B3J 2X4 (Canada); Bertuch, Adam; Sundaram, Ganesh [Ultratech Inc., Waltham, Massachusetts 02453 (United States)

2015-01-15

A method to enhance thermal microelectromechanical systems (MEMS) actuators in aqueous media by using dielectric encapsulation layers is presented. Aqueous media reduces the available mechanical energy of the thermal actuator through an electrical short between actuator structures. Al{sub 2}O{sub 3} and TiO{sub 2} laminates with various thicknesses were deposited on packaged PolyMUMPs devices to electrically separate the actuator from the aqueous media. Atomic layer deposition was used to form an encapsulation layer around released MEMS structures and the package. The enhancement was assessed by the increase of the elastic energy, which is proportional to the mechanical stiffness of the actuator and the displacement squared. The mechanical stiffness of the encapsulated actuators compared with the noncoated actuators was increased by factors ranging from 1.45 (for 45 nm Al{sub 2}O{sub 3} + 20 nm TiO{sub 2}) to 1.87 (for 90 nm Al{sub 2}O{sub 3} + 40 nm TiO{sub 2}). Displacement measurements were made for all laminate combinations in filtered tap water and seawater by using FFT based displacement measurement technique with a repeatability of ∼10 nm. For all laminate structures, the elastic energy increased and enhanced the actuator performance: In seawater, the mechanical output energy increased by factors ranging from 5 (for 90 nm Al{sub 2}O{sub 3}) to 11 (for 90 nm Al{sub 2}O{sub 3} + 40 nm TiO{sub 2}). The authors also measured the long-term actuator stability/reliability in seawater. Samples were stored for 29 days in seawater and tested for 17 days in seawater. Laminates with TiO{sub 2} layers allowed constant operation over the entire measurement period.

Polarografic study about the complex formation between indium (III) and sodium azide, in aqueous media

International Nuclear Information System (INIS)

Tokoro, R.; Bertotti, M.

1988-01-01

The present work is a branch of the main work concerned with the complex formation between several metal cations and azide ligand in aqueous media. The polarographic behavior of indium in azide system showed the tendency of complexation. Using polarographic method to determine the half potential of indium at each analytical concentration afforded experimental data to evaluate the constants. The azide concentrations was modified from 1 m to 100 m , the ionic strength held at 2,0 M with sodium perchlorate, indium concentration 7.892 x 10 -4 M, and temperature kept constant at 25,0 0 C. (author) [pt

Optical reading of contaminants in aqueous media based on gold nanoparticles.

Science.gov (United States)

Du, Jianjun; Zhu, Bowen; Peng, Xiaojun; Chen, Xiaodong

2014-09-10

With increasing trends of global population growth, urbanization, pollution over-exploitation, and climate change, the safe water supply has become a global issue and is threatening our society in terms of sustainable development. Therefore, there is a growing need for a water-monitoring platform with the capability of rapidness, specificity, low-cost, and robustness. This review summarizes the recent developments in the design and application of gold nanoparticles (AuNPs) based optical assays to detect contaminants in aqueous media with a high performance. First, a brief discussion on the correlation between the optical reading strategy and the optical properties of AuNPs is presented. Then, we summarize the principle behind AuNP-based optical assays to detect different contaminants, such as toxic metal ion, anion, and pesticides, according to different optical reading strategies: colorimetry, scattering, and fluorescence. Finally, the comparison of these assays and the outlook of AuNP-based optical detection are discussed. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Miswak mediated green synthesized palladium nanoparticles as effective catalysts for the Suzuki coupling reactions in aqueous media

Directory of Open Access Journals (Sweden)

Mujeeb Khan

2017-05-01

Full Text Available Green and eco-friendly synthesis of palladium nanoparticles NPs is carried out under facile and eco-friendly conditions using an aqueous solution of Salvadora persica L. (SP root extract (RE as a bioreductant, which is commonly known as Miswak. The as-synthesized Pd NPs were characterized using various spectroscopic and microscopic techniques, including, UV–Vis spectroscopy, FT-IR spectroscopy, XRD, ICP-MS and TEM. Detailed investigations of the Pd NPs have confirmed that the polyphenolic phytomolecules present in the RE of Miswak not only act as a bioreductant by facilitating the reduction and growth of Pd NPs, but they also functionalize the surface of Pd NPs and stabilized them in various solvents. Furthermore, the catalytic activity of the green synthesized Pd NPs was also tested toward the Suzuki coupling reactions of various aryl halides in aqueous media. The as-prepared Pd NPs exhibited superior catalytic activity and reusability for the Suzuki coupling reaction in aqueous and aerobic conditions. The kinetics of the reaction studied by GC revealed that the conversion of various aryl halides to biphenyl takes place in a short time.

Corrosion inhibitors for neutral aqueous media based on the products on sugar cane processing. 1.Furfural derivatives as inhibitors

International Nuclear Information System (INIS)

Ledovskikh, V.M.; Kamekho Khinnebra, Kh.Kh.

1993-01-01

A series of carboxy-, nitrogen- and nitroderivaties of furfural - the main product of sugar cane processing (furancasboxylic acid, 5-nitrofurancarboxylic acid and its salts, furfurine, furfurylamine) was studied as inhibitors of iron and copper, corrosion in aqueous-salt media. Nitrofuroates of sodium and ammonium, which decelerate anode process, intensity cathode one and provide the stable passive state, are considered to be the most effective

The Homocoupling Reaction of Aromatic Terminal Alkynes by a Highly Active Palladium(II)/AgNO₃ Cocatalyst in Aqueous Media Under Aerobic Conditions.

Science.gov (United States)

Guo, Mengping; Chen, Bo; Lv, Meiyun; Zhou, Xiuling; Wen, Yongju; Shen, Xiuli

2016-05-10

A new and efficient Pd(II)/AgNO₃-cocatalyzed homocoupling of aromatic terminal alkynes is described. Various symmetrical 1,4-disubstituted-1,3-diynes are obtained in good to excellent yields. This protocol employs a loading with relatively low palladium(II) in aqueous media under aerobic conditions.

The IUPAC aqueous and non-aqueous experimental pKa data repositories of organic acids and bases.

Science.gov (United States)

Slater, Anthony Michael

2014-10-01

Accurate and well-curated experimental pKa data of organic acids and bases in both aqueous and non-aqueous media are invaluable in many areas of chemical research, including pharmaceutical, agrochemical, specialty chemical and property prediction research. In pharmaceutical research, pKa data are relevant in ligand design, protein binding, absorption, distribution, metabolism, elimination as well as solubility and dissolution rate. The pKa data compilations of the International Union of Pure and Applied Chemistry, originally in book form, have been carefully converted into computer-readable form, with value being added in the process, in the form of ionisation assignments and tautomer enumeration. These compilations offer a broad range of chemistry in both aqueous and non-aqueous media and the experimental conditions and original reference for all pKa determinations are supplied. The statistics for these compilations are presented and the utility of the computer-readable form of these compilations is examined in comparison to other pKa compilations. Finally, information is provided about how to access these databases.

Formation and reactions of radical cations of substituted benzenes in aqueous media

International Nuclear Information System (INIS)

Holcman, J.

1977-08-01

Radical cations of anisole, methylated benzenes, ethylbenzene, isopropylbenzene, tert-butylbenzene and N,N-dimethylaniline were studied in aqueous media by pulse radiolytic technique. Absorption spectra and reaction kinetics of the radical cations were recorded. The radical cations are formed from the corresponding OH adducts by the elimination of OH - , either by a simple dissociation or by an acid catalyzed reaction. The rate constants of the formation of the radical cations and their reactions with water, OH - and Fe 2+ , or the reaction of a proton loss, were measured. The rate constants for the reaction with water and OH - , together with the rate constants for the dissociation of the OH adducts, are correlated with the ionization potential of the parent compound. These correlations offer a possibility of predicting the acid-base properties of radical cations of substituted benzenes, or the estimation of their ionization potential. (author)

Influence of additives on thermoresponsive polymers in aqueous media: a case study of poly(N-isopropylacrylamide).

Science.gov (United States)

Umapathi, Reddicherla; Reddy, P Madhusudhana; Rani, Anjeeta; Venkatesu, Pannuru

2018-04-18

Thermoresponsive polymers (TRPs) in different solvent media have been studied over a long period and are important from both scientific and technical points of view. Despite numerous studies on the behavior of TRPs with various additives, the interactions of additives with TRPs are still poorly understood. Moreover, despite the vast available literature regarding the biomolecular interactions between various TRPs and naturally occurring additives, it is not possible to provide a unifying declaration about the behavior of different additives, in particular at the phase transition temperature of the polymer. However, potential reviews that describe the behavior of additives as stimuli upon the phase transition of TRPs are also absent. A lack of sufficient knowledge regarding the responses of TRPs to additives as stimuli has hindered the expansion of the wide spectrum of applications of these polymers. Therefore, it was proposed to review the responses of TRPs in the presence of various additives in aqueous media. In-depth knowledge acquired via a literature survey has drawn our attention towards filling this gap by analyzing the interactions of TRPs with different additives. In this perspective, we have systematically examined the stability, aggregation, and phase transition behaviours of various polymers in the presence of different additives. The perspective on the influence of additives as stimuli on the behavior of TRPs in an aqueous medium will provide new reliable information about intramolecular interactions between interior polymer segments as well as intermolecular interactions between TRPs and additive molecules, which will be helpful for industrialists in the preparation of new polymeric materials for drug-delivery systems.

Principles of interactions in non-aqueous electrolyte solutions

NARCIS (Netherlands)

Lyklema, J.

2013-01-01

In this paper a review is presented on the molecular interactions in non-aqueous media of low dielectric permittivity. Qualitative and quantitative distinctions with aqueous solutions are emphasized. The reviewed themes include dispersion forces, dissociation and association equilibria,

Speciation of organotin compounds by capillary electrophoresis: comparison of aqueous and mixed organic-aqueous systems

Energy Technology Data Exchange (ETDEWEB)

Guo, Lei; Matysik, Frank-Michael; Glaeser, Petra [Universitaet Leipzig, Institut fuer Analytische Chemie, Leipzig (Germany)

2004-10-01

A capillary electrophoresis method with direct ultraviolet detection was developed for the analysis of organotin species. Despite the fact that direct detection of organotin compounds by ultraviolet absorption is difficult because most organotins possess poor chromophoric properties, the application of low wavelength ({lambda}=200 nm) and mixed organic-aqueous media enabled a significant enhancement in sensitivity. A mixed organic-aqueous system (10% methanol/40% acetonitrile/50% H{sub 2}O) containing acetic acid and tetrabutylammonium perchlorate formed the basis for rapid, efficient and sensitive determinations of organotin cations such as tripropyltin, tributyltin, triphenyltin and diphenyltin. The concentration limits of detection (LOD) for the four organotin compounds were in the range of 0.4-14 {mu}M, comparable to that obtained with the most sensitive indirect UV method reported until now, and took advantage of a stable baseline, a symmetric peak shape and an absence of disturbing system peaks. The relative standard deviations (n=7) for the relative peak time and peak area were 0.44-0.77 and 4.8-5.8%, respectively. In addition to sensitivity enhancements, the use of organic-aqueous systems instead of pure aqueous media resulted in improved selectivity and efficiency of separations. (orig.)

One-Pot Synthesis of Some New Pyrido[2,3-d]pyrimidine Derivatives Catalyzed by Sodium Lauryl Sulfate in Aqueous Media

Directory of Open Access Journals (Sweden)

Sheng-Hui Li

2010-01-01

Full Text Available A series of pyrido[2,3-d]pyrimidine derivatives were synthesized by the three-component reaction of aromatic aldehyde, malononitrile and 6-amino-4-hydroxy-2-mercaptopyrimidine catalyzed by sodium lauryl sulfate (SDS in aqueous media. It was interesting that further aromatization took place automatically. This method provides several advantages such as easier work-up, milder reaction conditions and environmental friendly.

Metal-Catalyzed Intra- and Intermolecular Addition of Carboxylic Acids to Alkynes in Aqueous Media: A Review

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Javier Francos

2017-11-01

Full Text Available The metal-catalyzed addition of carboxylic acids to alkynes is a very effective tool for the synthesis of carboxylate-functionalized olefinic compounds in an atom-economical manner. Thus, a large variety of synthetically useful lactones and enol-esters can be accessed through the intra- or intermolecular versions of this process. In order to reduce the environmental impact of these reactions, considerable efforts have been devoted in recent years to the development of catalytic systems able to operate in aqueous media, which represent a real challenge taking into account the tendency of alkynes to undergo hydration in the presence of transition metals. Despite this, different Pd, Pt, Au, Cu and Ru catalysts capable of promoting the intra- and intermolecular addition of carboxylic acids to alkynes in a selective manner in aqueous environments have appeared in the literature. In this review article, an overview of this chemistry is provided. The synthesis of β-oxo esters by catalytic addition of carboxylic acids to terminal propargylic alcohols in water is also discussed.

Silver nanoparticles embedded polymer sorbent for preconcentration of uranium from bio-aggressive aqueous media

International Nuclear Information System (INIS)

Das, Sadananda; Pandey, Ashok K.; Athawale, Anjali A.; Subramanian, M.; Seshagiri, T.K.; Khanna, Pawan K.; Manchanda, Vijay K.

2011-01-01

Adsorptive sorbent for bio-aggressive natural aqueous media like seawater was developed by one pot simultaneous synthesis of silver nanoparticles (Ag nps) and poly(ethylene glycol methacrylate phosphate) (PEGMP) by UV-initiator induced photo-polymerization. The photo-polymerization was carried out by irradiating N,N'-dimethylformamide (DMF) solution containing appropriate amounts of the functional monomer (ethylene glycol methacrylate phosphate), UV initiator (α,α'-dimethoxy-α-phenyl acetophenone), and Ag + ions with 365 nm UV light in a multilamps photoreactor. To increase mechanical strength, nano-composite sorbent (Ag-PEGMP) was also reinforced with thermally bonded non-woven poly(propylene) fibrous sheet. Transmission electron microscopy (TEM) of the nano-composite sorbent showed uniform distribution of spherical Ag nanoparticles with particles size ranging from 3 to 6 nm. The maximum amount of Ag 0 that could be anchored in the form of nanoparticles were 5 ± 1 and 10 ± 1 wt.% in self-supported PEGMP and poly(propylene) reinforced PEGMP matrices, respectively. Ag-PEGMP sorbent was found to be stable under ambient conditions for a period of six months. Ag-PEGMP composite sorbent did not exhibit growth at all after incubation with pre-grown Escherichia coli cells, and showed non-adherence of this bacteria to the composite. This indicated that composite sorbent has the bio-resistivity due to bacterial repulsion and bactericidal properties of Ag nanoparticles embedded in the PEGMP. Sorption of U(VI) in PEGMP and Ag-PEGMP nano-composite sorbents from well-stirred seawater was studied to explore the possibility of using it for uranium preconcentration from bio-aggressive aqueous streams. The nano-composite sorbent was used to preconcentrate U(VI) from a process aqueous waste stream.

Effect of alpha irradiation on UO2 surface reactivity in aqueous media

International Nuclear Information System (INIS)

Jegou, C.; Muzeau, B.; Broudic, V.; Poulesquen, A.; Roudil, D.; Jorion, F.; Corbel, C.

2005-01-01

The option of direct disposal of spent nuclear fuel in a deep geological formation raises the need to investigate the long-term behavior of the UO 2 matrix in aqueous media subjected to α-β-γ radiation. The β-γ emitters account for most of the activity of spent fuel at the moment it is removed from the reactor, but diminish within a millennial time frame by over three orders of magnitude to less than the long-term activity. The latter persists over much longer time periods and must therefore be taken into account over a geological disposal time scale. Leaching experiments with solution renewal were carried out on UO 2 pellets doped with alpha emitters ( 238 Pu and 239 Pu) to quantify the impact of alpha irradiation on UO 2 matrix alteration. Three batches of doped UO 2 pellets with different alpha flux levels (3.30 x 10 4 , 3.30 x 10 5 , and 3.2 x 10 6 α cm -2 s -1 ) were studied. The results obtained in aerated and deaerated media immediately after sample annealing or interim storage in air provide a better understanding of the UO 2 matrix alteration mechanisms under alpha irradiation. Interim storage in air of UO 2 pellets doped with alpha emitters results in variations of the UO 2 surface reactivity, which depends on the alpha particle flux at the interface and on the interim storage duration. The variation in the surface reactivity and the greater uranium release following interim storage cannot be attributed to the effect of alpha radiolysis in aerated media since the uranium release tends toward the same value after several leaching cycles for the doped UO 2 pellet batches and spent fuel. Oxygen diffusion enhanced by alpha irradiation of the extreme surface layer and/or radiolysis of the air could account for the oxidation of the surface UO 2 to UO 2+x . However, leaching experiments performed in deaerated media after annealing the samples and preleaching the surface suggest that alpha radiolysis does indeed affect the dissolution, which varies with the

New ceramics incorporated with industrial by-products as pore formers for sorption of toxic chromium from aqueous media

Science.gov (United States)

Domopoulou, Artemi

2015-04-01

The incorporation of secondary resources including various industrial wastes as pore-forming agents into clayey raw material mixtures for the development of tailored porous ceramic microstructures is currently of increasing interest. In the present research, sintered ceramic compacts were developed incorporated with industrial solid by-products as pore formers, and then used as new sorbents for chromium removal from aqueous media. The microstructures obtained were characterized through X-ray diffraction (XRD) analysis as well as scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectrometry (EDX). Sorption potential of chromium from synthetic solutions on the porous ceramics was studied by static adsorption experiments as a function of the pore-former percentage in the ceramic matrix as well as the initial heavy metal (chromium) concentration, solution pH and temperature. Kinetic studies were conducted and adsorption isotherms of chromium were determined using the Langmuir equation. Preliminary experimental results concerning the adsorption characteristics of chromium on the ceramic materials produced appear encouraging for their possible beneficial use as new sorbents for the removal of toxic chromium from aqueous media. Keywords: sorbents, ceramics, industrial solid by-products, pore-former, chromium. Acknowledgements: This research has been co-financed by the European Union (European Social Fund - ESF) and Greek national funds through the Operational Program "Education and Lifelong Learning" of the National Strategic Reference Framework (NSRF) - Research Funding Program ARCHIMEDES III: Investing in knowledge society through the European Social Fund.

Formation of magnetite (Fe3O4)in aqueous media and properties of the interface magnetite/solution

International Nuclear Information System (INIS)

Regazzoni, A.E.

1984-01-01

The formation of Fe 3 O 4 particles in aqueous media and the properties of the Fe 3 O 4 /aqueous solution interface are studied. This system is of particular interest in nuclear reactor chemistry, since Fe 3 O 4 was identified as the main component of the corrosion products of nuclear power plants cooled with pressurized water, of the Atucha I and II, and Embalse type. Four methods for the synthesis of Fe 3 O 4 are described: a) controlled oxidation of Fe(OH) 2 in the presence of NaNO 3 at 25 deg C; b) controlled oxidation of Fe(OH) 2 in the presence of NaNO 3 and N 2 H 4 and at 100 deg C; c) alkalinization of a F 2+ and Fe 3+ solutions at 80 deg C; d) simultaneous oxidation and alkalinization of a Fe 2+ . The interfacial properties of Fe 3 O 4 particles suspended in aqueous solutions of indifferent electrolytes are described. These properties are essential for the activity transport associated with the corrosion products. Finally, the adsorption of H 3 BO 3 , Hsub(n)PO 4 sup(n-3) and n Co(II) in the Fe 3 O 4 /solution interface at 30 deg C. It is concluded that the adsorbed species are chemically bonded to surface metal ions. (M.E.L.) [es

Electrochemical Oxidation of Silver and Copper in Aqueous Basic Media and in Fused Hydroxide Electrolytes

Directory of Open Access Journals (Sweden)

Tejada-Rosales, E. M.

2004-04-01

Full Text Available The anodic oxidations of copper and silver electrodes in basic media are reported. Experiments were conducted both in aqueous NaOH solutions and in a flux of molten NaOH/KOH eutectic. The oxidation processes were studied by means of cyclic voltammetry and chronoamperometries and the phases obtained were systematically characterized by x-ray diffraction. The ranges of stability of each phase in the different media studied are reported. In addition to known oxides of copper or silver, a new silver oxide was isolated.

En este trabajo se describe la oxidación anódico de electrodos de plata y de cobre en medios básicos. Se han utilizado tanto medios acuosos como hidróxidos fundidos (eutéctico NaOH/KOH. Los procesos de oxidación se han estudiado mediante voltametría cíclica y cronoamperometría, y las fases resultantes han sido caracterizadas por difracción de Rayos X. Los rangos de estabilidad encontrados para cada uno dependen del medio utilizado. Además de óxidos conocidos de cobre y de plata, se ha aislado un nuevo óxido de plata.

Synthesis of highly luminescent Mn:ZnSe/ZnS nanocrystals in aqueous media

International Nuclear Information System (INIS)

Fang Zheng; Wu Ping; Zhong Xinhua; Yang Yongji

2010-01-01

High-quality water-dispersible Mn 2+ -doped ZnSe core/ZnS shell (Mn:ZnSe/ZnS) nanocrystals have been synthesized directly in aqueous media. Overcoating a high bandgap ZnS shell around the Mn:ZnSe cores can bring forward an efficient energy transfer from the ZnSe host nanocrystals to the dopant Mn. The quantum yields of the dopant Mn photoluminescence in the as-prepared water-soluble Mn:ZnSe/ZnS core/shell nanocrystals can be up to 35 ± 5%. The optical features and structure of the obtained Mn:ZnSe/ZnS core/shell nanocrystals have been characterized by UV-vis, PL spectroscopy, TEM, XRD and ICP elementary analysis. The influences of various experimental variables, including the Mn concentration, the Se/Zn molar ratio as well as the kind and amount of capping ligand used in the core production and shell deposition process, on the luminescent properties of the obtained Mn:ZnSe/ZnS nanocrystals have been systematically investigated.

Effect of alpha irradiation on UO{sub 2} surface reactivity in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Jegou, C.; Muzeau, B.; Broudic, V.; Poulesquen, A.; Roudil, D. [Commissariat a l' Energie Atomique (CEA), Rhone Valley Research Center, DIEC/SESC/LMPA, Bagnols-sur-Ceze (France); Jorion, F. [Commissariat a l' Energie Atomique (CEA), Rhone Valley Research Center, DRCP/SE2A/LEMA, Bagnols-sur-Ceze (France); Corbel, C. [Commissariat a l' Energie Atomique (CEA), Saclay Research Center, DSM/DRECAM/SCM, Gif sur Yvette (France)

2005-07-01

The option of direct disposal of spent nuclear fuel in a deep geological formation raises the need to investigate the long-term behavior of the UO{sub 2} matrix in aqueous media subjected to {alpha}-{beta}-{gamma} radiation. The {beta}-{gamma} emitters account for most of the activity of spent fuel at the moment it is removed from the reactor, but diminish within a millennial time frame by over three orders of magnitude to less than the long-term activity. The latter persists over much longer time periods and must therefore be taken into account over a geological disposal time scale. Leaching experiments with solution renewal were carried out on UO{sub 2} pellets doped with alpha emitters ({sup 238}Pu and {sup 239}Pu) to quantify the impact of alpha irradiation on UO{sub 2} matrix alteration. Three batches of doped UO{sub 2} pellets with different alpha flux levels (3.30 x 10{sup 4}, 3.30 x 10{sup 5}, and 3.2 x 10{sup 6} {alpha} cm{sup -2} s{sup -1}) were studied. The results obtained in aerated and deaerated media immediately after sample annealing or interim storage in air provide a better understanding of the UO{sub 2} matrix alteration mechanisms under alpha irradiation. Interim storage in air of UO{sub 2} pellets doped with alpha emitters results in variations of the UO{sub 2} surface reactivity, which depends on the alpha particle flux at the interface and on the interim storage duration. The variation in the surface reactivity and the greater uranium release following interim storage cannot be attributed to the effect of alpha radiolysis in aerated media since the uranium release tends toward the same value after several leaching cycles for the doped UO{sub 2} pellet batches and spent fuel. Oxygen diffusion enhanced by alpha irradiation of the extreme surface layer and/or radiolysis of the air could account for the oxidation of the surface UO{sub 2} to UO{sub 2+x}. However, leaching experiments performed in deaerated media after annealing the samples and

New thiamine functionalized silica microparticules as a sorbent for the removal of lead, mercury and cadmium ions in aqueous media

Directory of Open Access Journals (Sweden)

Deniz Sabahattin

2017-01-01

Full Text Available The existence of heavy metal ions in aqueous media is one of the biggest environmental pollution problems and thus the removal of heavy metals is a very important procedure. In this work, a new adsorbent was synthesized by modifying 3-aminopropyl-functionalized silica gel with thiamine (vitamin B1 and characterized. The influence of the uptake conditions, such as pH, contact time, initial feed concentration and foreign metal ions, on the binding capacity of thiamine-functionalized silica gel sorbent (M3APS were investigated. Maximum obtained adsorption capacities for Pb(II, Hg(II and Cd(II were 39.4±0.2, 30.9±0.5 and 9.54±0.4 mg g-1 M3APS, respectively, at pH 5.0. The observed selectivity of M3APS for these metal ions was the following: Pb(II > Hg(II > Cd(II. Adsorption isotherm models were also applied to the adsorption process. As a result, the Langmuir isotherm model gave the best fit for the adsorption of metal ions on M3APS. The Gibbs energy change (ΔG for the adsorption of Pb(II, Hg(II and Cd(II were calculated to predict the nature of adsorption process. Having such satisfactory adsorption results, M3APS is a potential candidate adsorbent for Pb(II and Hg(II removal from aqueous media.

A novel double-layer molecularly imprinted polymer film based surface plasmon resonance for determination of testosterone in aqueous media

International Nuclear Information System (INIS)

Tan, Yuan; Jing, Lijing; Ding, Yonghong; Wei, Tianxin

2015-01-01

Highlights: • The in-situ photo-grafting polymerization method was used to prepare the polymer film. • The synthesized MIF was layer stucture film. • The MIF exhibited good imprinting effect and highly selectivity. - Abstract: This work aimed to prepare a novel double-layer structure molecularly imprinted polymer film (MIF) on the surface plasmon resonance (SPR) sensor chips for detection of testosterone in aqueous media. The film was synthesized by in-situ UV photo polymerization. Firstly, the modification of gold surface of SPR chip was performed by 1-dodecanethiol. Then double-layer MIF was generated on the 1-dodecanethiol modified gold surface. The non-modified and imprinted surfaces were characterized by atomic force microscopy (AFM), fourier transform infrared (FTIR) spectroscopy and contact angle measurements. Analysis of SPR spectroscopy showed that the imprinted sensing film displayed good selectivity for testosterone compared to other analogues and the non-imprinted polymer film (NIF). Within the concentrations range of 1 × 10 −12 –1 × 10 −8 mol/L, the coupling angle changes of SPR were linear with the negative logarithm of testosterone concentrations (R 2 = 0.993). Based on a signal/noise ratio of three, the detection limit was estimated to be 10 −12 mol/L. Finally, the developed MIF was successfully applied to the seawater detection of testosterone. The results in the experiments suggested that a combination of SPR sensing with MIF was a promising alternative method for detection of testosterone in aqueous media

Study of the europium behavior in aqueous media; Estudio sobre el comportamiento del europio en medios acuosos

Energy Technology Data Exchange (ETDEWEB)

Fernandez R, E.; Jimenez R, M.; Solache R, M.; Martinez M, V. [Instituto Nacional de Investigaciones Nucleares, Departamento de Quimica, A.P. 18-1027, C.P. 11801 Mexico D.F. (Mexico)

2000-07-01

Europium as waste can produce a pollution problem in water that is in contact with it, what would has a heavy environmental impacts, because of the possibilities of diffusion of these wastes from their place of confinement or storage until the geo and biosphere. The solution of such problem requires of a lot of knowledge over the behavior of several chemical elements such as europium in aqueous solutions. In this work it was used a low ion force (0.02 M). The data set will allow extrapolate the hydrolytic behavior of europium in too much minors ion force media, such as the ground waters, including in ion force zero.

PENGEMBANGAN METODE SINTESIS FURFURAL BERBAHAN DASAR CAMPURAN LIMBAH PERTANIAN DALAM RANGKA MEWUJUDKAN PRINSIP GREEN CHEMISTRY (Development Of Synthesis Method Of Furfural From Compost Heap Mixture To Reach Out Green Chemistry Principles

Directory of Open Access Journals (Sweden)

Mitarlis Mitarlis

2011-11-01

Full Text Available ABSTRAK Penelitian pengembangan metode sintesis furfural dengan bahan dasar campuran limbah pertanian dilakukan dengan tujuan untuk menentukan waktu pemanasan dan konsentrasi asam optimum serta mewujudkan prinsip green chemistry. Dalam penelitian ini digunakan campuran limbah pertanian ampas tebu, limbah daun nanas dan limbah tanaman jagung dengan perbandingan 1:1:1. Proses sintesis melalui tahap hidrolisis pentosan, dehidrasi, dan siklodehidrasi untuk membentuk furfural dengan menggunakan alat refluks termodifkasi. Identifikasi furfural menggunakan uji warna dengan anilin asetat, uji indeks bias, spektrofotometer UV-Vis, dan IR, serta GC. Analisis pemenuhan prinsip green chemistry menggunakan daftar ceck 12 prinsip green chemstry. Hasil penelitian menunjukkan bahwa: Waktu pemanasan dan konsentrasi asam sulfat optimum pada pembuatan furfural dari campuran limbah pertanian adalah 5 jam dan konsentrasi asam sulfat 10% (1,876 M dengan rendemen sebesar 5,58%. Metode sintesis furfural yang dikembangkan dapat memenuhi 11 dari 12 prinsip green chemistry yang telah ditetapkan. ABSTRACT The study of developing furfural synthesis method  from  compost heap mixture had been done to determine  optimum condition for this process and  to reach out the green chemistry principles. In this research, the compost heap mixture is from three kinds of compost heap (bagasse, pineapple leaf, waste of corn plant with same amount (1:1:1. The steps of furfural production process are hydrolysis of pentose by sulfuric acid, dehydration, and cyclodehydration to form furfural. It was produced by using a modification reflux apparatus. Identify of furfural product by  using qualitative analysis color test with aniline acetate, refractive index test, UV-Vis,  IR spectrophotometer, and GC. Green chemistry principles are analyzed by using check list of 12 principles of green chemistry.  Based on this research was obtained that the optimum concentration of sulfuric acid is

Absorption mechanisms for cationic and anionic mineral species on ferric iron polymer hydroxides and oxidation products of ferrous iron in aqueous media

International Nuclear Information System (INIS)

Gandon, Remi

1982-01-01

Adsorbents obtained by hydrolysing the Fe 3+ , 6H 2 O ion are made of polymers with aquo (H 2 O), hydroxo (-OH...) and oxo (...O...) ligands. Radioactive tracers reveal the importance of chemical mechanisms in adsorption phenomena on ferric oxide in aqueous media. Zn 2+ , Co 2+ and Mn 2+ cations are exchanged with hydrogen from hydroxo groups. CrO 4 2- , SeO 3 2- and Sb(OH) 6 - anions form covalent associations in place of iron ligands. The adsorption of hydrolyzed ions results in strong oxygen bridge bonds. In fresh water, Co and Mn participate alone in physical electrostatic adsorption. Iron II oxidation products generate chemical adsorptions. Zn 2+ and Sb(OH) 6 - associate with ferric hydroxides from oxidized Fe 2+ . 60 Co, 54 Mn and 51 Cr form covalent associations between unpaired 3d iron electrons and the adsorbed element. This process is not predominant with selenium IV or VI reduced to the metallic state or fixed on ferric hydroxide in the selenite form. These conclusions can be applied to pollutant analysis and to water purification and contribute to our understanding of the role of iron in the distribution of oligo-elements in aqueous media. (author) [fr

A facile approach for cupric ion detection in aqueous media using polyethyleneimine/PMMA core-shell fluorescent nanoparticles

International Nuclear Information System (INIS)

Chen Jian; Zeng Fang; Wu Shuizhu; Su Junhua; Zhao Jianqing; Tong Zhen

2009-01-01

A facile approach was developed to produce a dye-doped core-shell nanoparticle chemosensor for detecting Cu 2+ in aqueous media. The core-shell nanoparticle sensor was prepared by a one-step emulsifier-free polymerization, followed by the doping of the fluorescent dye Nile red (9-diethylamino- 5H-benzo[alpha] phenoxazine-5-one, NR) into the particles. For the nanoparticles, the hydrophilic polyethyleneimine (PEI) chain segments serve as the shell and the hydrophobic polymethyl methacrylate (PMMA) constitutes the core of the nanoparticles. The non-toxic and biocompatible PEI chain segments on the nanoparticle surface exhibit a high affinity for Cu 2+ ions in aqueous media, and the quenching of the NR fluorescence is observed upon binding of Cu 2+ ions. This makes the core-shell nanoparticle system a water-dispersible chemosensor for Cu 2+ ion detection. The quenching of fluorescence arises through intraparticle energy transfer (FRET) from the dye in the hydrophobic PMMA core to the Cu 2+ /PEI complexes on the nanoparticle surface. The energy transfer efficiency for PEI/PMMA particles with different diameters was determined, and it is found that the smaller nanoparticle sample exhibits higher quenching efficiency, and the limit for Cu 2+ detection is 1 μM for a nanoparticle sample with a diameter of ∼30 nm. The response of the fluorescent nanoparticle towards different metal ions was investigated and the nanoparticle chemosensor displays high selectivity and antidisturbance for the Cu 2+ ion among the metal ions examined (Na + , K + , Mg 2+ , Ca 2+ , Zn 2+ , Hg 2+ , Mn 2+ , Fe 2+ , Ni 2+ , Co 2+ and Pb 2+ ). This emulsifier-free, biocompatible and sensitive fluorescent nanoparticle sensor may find applications in cupric ion detection in the biological and environmental areas.

A facile approach for cupric ion detection in aqueous media using polyethyleneimine/PMMA core-shell fluorescent nanoparticles.

Science.gov (United States)

Chen, Jian; Zeng, Fang; Wu, Shuizhu; Su, Junhua; Zhao, Jianqing; Tong, Zhen

2009-09-09

A facile approach was developed to produce a dye-doped core-shell nanoparticle chemosensor for detecting Cu(2+) in aqueous media. The core-shell nanoparticle sensor was prepared by a one-step emulsifier-free polymerization, followed by the doping of the fluorescent dye Nile red (9-diethylamino- 5H-benzo[alpha] phenoxazine-5-one, NR) into the particles. For the nanoparticles, the hydrophilic polyethyleneimine (PEI) chain segments serve as the shell and the hydrophobic polymethyl methacrylate (PMMA) constitutes the core of the nanoparticles. The non-toxic and biocompatible PEI chain segments on the nanoparticle surface exhibit a high affinity for Cu(2+) ions in aqueous media, and the quenching of the NR fluorescence is observed upon binding of Cu(2+) ions. This makes the core-shell nanoparticle system a water-dispersible chemosensor for Cu(2+) ion detection. The quenching of fluorescence arises through intraparticle energy transfer (FRET) from the dye in the hydrophobic PMMA core to the Cu(2+)/PEI complexes on the nanoparticle surface. The energy transfer efficiency for PEI/PMMA particles with different diameters was determined, and it is found that the smaller nanoparticle sample exhibits higher quenching efficiency, and the limit for Cu(2+) detection is 1 microM for a nanoparticle sample with a diameter of approximately 30 nm. The response of the fluorescent nanoparticle towards different metal ions was investigated and the nanoparticle chemosensor displays high selectivity and antidisturbance for the Cu(2+) ion among the metal ions examined (Na(+), K(+), Mg(2+), Ca(2+), Zn(2+), Hg(2+), Mn(2+), Fe(2+), Ni(2+), Co(2+) and Pb(2+)). This emulsifier-free, biocompatible and sensitive fluorescent nanoparticle sensor may find applications in cupric ion detection in the biological and environmental areas.

A facile approach for cupric ion detection in aqueous media using polyethyleneimine/PMMA core-shell fluorescent nanoparticles

Science.gov (United States)

Chen, Jian; Zeng, Fang; Wu, Shuizhu; Su, Junhua; Zhao, Jianqing; Tong, Zhen

2009-09-01

A facile approach was developed to produce a dye-doped core-shell nanoparticle chemosensor for detecting Cu2+ in aqueous media. The core-shell nanoparticle sensor was prepared by a one-step emulsifier-free polymerization, followed by the doping of the fluorescent dye Nile red (9-diethylamino- 5H-benzo[alpha] phenoxazine-5-one, NR) into the particles. For the nanoparticles, the hydrophilic polyethyleneimine (PEI) chain segments serve as the shell and the hydrophobic polymethyl methacrylate (PMMA) constitutes the core of the nanoparticles. The non-toxic and biocompatible PEI chain segments on the nanoparticle surface exhibit a high affinity for Cu2+ ions in aqueous media, and the quenching of the NR fluorescence is observed upon binding of Cu2+ ions. This makes the core-shell nanoparticle system a water-dispersible chemosensor for Cu2+ ion detection. The quenching of fluorescence arises through intraparticle energy transfer (FRET) from the dye in the hydrophobic PMMA core to the Cu2+/PEI complexes on the nanoparticle surface. The energy transfer efficiency for PEI/PMMA particles with different diameters was determined, and it is found that the smaller nanoparticle sample exhibits higher quenching efficiency, and the limit for Cu2+ detection is 1 µM for a nanoparticle sample with a diameter of ~30 nm. The response of the fluorescent nanoparticle towards different metal ions was investigated and the nanoparticle chemosensor displays high selectivity and antidisturbance for the Cu2+ ion among the metal ions examined (Na+, K+, Mg2+, Ca2+, Zn2+, Hg2+, Mn2+, Fe2+, Ni2+, Co2+ and Pb2+). This emulsifier-free, biocompatible and sensitive fluorescent nanoparticle sensor may find applications in cupric ion detection in the biological and environmental areas.

Protonation site for anilines in aqueous media

Directory of Open Access Journals (Sweden)

INNA M. UCHAEVA

2002-02-01

Full Text Available By means of the PM3 method it has been shown that the protonation of 2-, 3-, 4-methoxyanilines, 4-methylthioaniline, 2-, 3-, 4-aminobenzoic acids, 2-, 3-, 4-nitroanilines in the gaseous phase proceeds via the amine nitrogen atom. The same result, attributed to the aqueous medium, was obtained for 4-methoxyaniline, 4-aminobenzoic acid and 4-nitroaniline.

A novel double-layer molecularly imprinted polymer film based surface plasmon resonance for determination of testosterone in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Tan, Yuan; Jing, Lijing; Ding, Yonghong; Wei, Tianxin, E-mail: txwei@bit.edu.cn

2015-07-01

Highlights: • The in-situ photo-grafting polymerization method was used to prepare the polymer film. • The synthesized MIF was layer stucture film. • The MIF exhibited good imprinting effect and highly selectivity. - Abstract: This work aimed to prepare a novel double-layer structure molecularly imprinted polymer film (MIF) on the surface plasmon resonance (SPR) sensor chips for detection of testosterone in aqueous media. The film was synthesized by in-situ UV photo polymerization. Firstly, the modification of gold surface of SPR chip was performed by 1-dodecanethiol. Then double-layer MIF was generated on the 1-dodecanethiol modified gold surface. The non-modified and imprinted surfaces were characterized by atomic force microscopy (AFM), fourier transform infrared (FTIR) spectroscopy and contact angle measurements. Analysis of SPR spectroscopy showed that the imprinted sensing film displayed good selectivity for testosterone compared to other analogues and the non-imprinted polymer film (NIF). Within the concentrations range of 1 × 10{sup −12}–1 × 10{sup −8} mol/L, the coupling angle changes of SPR were linear with the negative logarithm of testosterone concentrations (R{sup 2} = 0.993). Based on a signal/noise ratio of three, the detection limit was estimated to be 10{sup −12} mol/L. Finally, the developed MIF was successfully applied to the seawater detection of testosterone. The results in the experiments suggested that a combination of SPR sensing with MIF was a promising alternative method for detection of testosterone in aqueous media.

Critical review of the chemistry and thermodynamics of technetium and some of its inorganic compounds and aqueous species

International Nuclear Information System (INIS)

Rard, J.A.

1983-01-01

Chemical and thermodynamic data for Technetium (Tc) and some of its inorganic compounds and aqueous species are reviewed here. Major emphasis is given to systems with potential geochemical applications, especially the geochemistry of radioactive waste disposal. Compounds considered include oxides, hydroxides, hydrates oxides, halides, oxyhalides, double halides, and sulfides. The aqueous species considered include those in both noncomplexing media (pertechnetates, technetates, aquo-ions, and hydrolyzed cations) and complexing media (halides, sulfates, and phosphates). Thermodynamic values are recommended for specific compounds and aqueous ions when reliable experimental data are available. Where thermodynamic data are inadequate or unavailable, the chemistry is still discussed to provide information about what needs to be measured, and which chemistry needs to be clarified. A major application of these thermodynamic data will be for chemical equilibrium modeling and for construction of potential-pH diagrams for aqueous solutions. Unfortunately, the present lack of data precludes such calculations for complexing aqueous media. The situation is much better for noncomplexing aqueous media, but the chemistry and thermodynamics of cationic Tc(V) species and hydrolyzed Tc(III) species are poorly understood. 240 references, 6 tables

Reactive transport of aqueous protons in porous media

KAUST Repository

McNeece, Colin J.; Hesse, Marc A.

2016-01-01

and total aqueous proton concentrations. An inflection point in this function near neutral pH leads to a reversal in the classic front formation mechanism under basic conditions, such that proton desorption leads to a self-sharpening front, while adsorption

Nanoparticulas basadas en complejos de Fe(II) con transicion de espin: sintesis, caracterizacion y aplicaciones en electronica molecular

Science.gov (United States)

Monrabal Capilla, Maria

Esta tesis doctoral esta organizada en 5 capitulos y esta destinada al estudio de sistemas de Fe (II) que presentan el fenomeno de la transicion de espin a escala nanometrica. El capitulo 1 contiene una introduccion general sobre materiales moleculares multifuncionales, destacando aquellos ejemplos mas importantes. Por otro lado, se explicara el fenomeno de la transicion de espin, tratando aspectos conceptuales, los antecedentes mas importantes y la situacion actual. En el capitulo 2 se describen los diferentes procesos existentes para la obtencion de diferentes tipos de nanoparticulas. Ademas, se presenta la sintesis y caracterizacion de nanoparticulas del polimero de coordinacion unidimensional [Fe(Htrz)2(trz)]BF4, obtenidas mediante el metodo de micelas inversas. Estas nanoparticulas, con una estrecha distribucion de tamanos centrada alrededor de los 11 nm, presentan una transicion de espin muy abrupta, con un ancho ciclo de histeresis termica de unos 40K. En el capitulo 3 se describe el proceso de modificacion del tamano de las nanoparticulas descritas en el capitulo anterior, llevado a cabo variando la proporcion de surfactante/H2O en el medio. Ademas, con el objetivo de modificar las propiedades magneticas de las nanoparticulas obtenidas en el capitulo 2, se lleva a cabo la sintesis de nanoparticulas de polimeros de la misma familia del [Fe(Htrz)2(trz)]BF4. En concreto se sintetizaron 3 nuevos tipos de nanoparticulas basadas en el polimero [Fe(Htrz)1-x(NH2trz)x](ClO4)2, siendo x = 0.05, 0.15 y 0.3, en cada caso. Estas nanoparticulas siguen presentando una estrecha distribucion de tamanos y una transicion de espin muy abrupta y con un ancho ciclo de histeresis. Ademas, se observa que este ciclo se desplaza a temperaturas mas proximas a la temperatura ambiente a medida que se aumenta el porcentaje de 4-amino-1, 2, 4- triazol en la muestra. Pero al mismo tiempo se produce una disminucion de la anchura de este ciclo. Por ultimo, en este capitulo se presenta la

Comparative Studies on Conventional and Ultrasound-Assisted Synthesis of Novel Homoallylic Alcohol Derivatives Linked to Sulfonyl Dibenzene Moiety in Aqueous Media

Directory of Open Access Journals (Sweden)

Mohamed F. Mady

2013-01-01

Full Text Available Novel homoallylic alcohols incorporating sulfone moieties were synthesized by the treatment of different carbonyl compounds with allylic bromides in aqueous media via sonochemical Barbier-type reaction conditions. Sulfonation of α-bromoketones with sodium benzenesulfinate in presence of CuI/2,6-lutidine rapidly gave β-keto-sulfones in good yields. In general, ultrasound irradiation offered the advantages of high yields, short reaction times, and simplicity compared to the conventional methods. The structures of all the compounds were confirmed by analytical and spectral data.

How Solid-Electrolyte Interphase Forms in Aqueous Electrolytes.

Science.gov (United States)

Suo, Liumin; Oh, Dahyun; Lin, Yuxiao; Zhuo, Zengqing; Borodin, Oleg; Gao, Tao; Wang, Fei; Kushima, Akihiro; Wang, Ziqiang; Kim, Ho-Cheol; Qi, Yue; Yang, Wanli; Pan, Feng; Li, Ju; Xu, Kang; Wang, Chunsheng

2017-12-27

Solid-electrolyte interphase (SEI) is the key component that enables all advanced electrochemical devices, the best representative of which is Li-ion battery (LIB). It kinetically stabilizes electrolytes at potentials far beyond their thermodynamic stability limits, so that cell reactions could proceed reversibly. Its ad hoc chemistry and formation mechanism has been a topic under intensive investigation since the first commercialization of LIB 25 years ago. Traditionally SEI can only be formed in nonaqueous electrolytes. However, recent efforts successfully transplanted this concept into aqueous media, leading to significant expansion in the electrochemical stability window of aqueous electrolytes from 1.23 V to beyond 4.0 V. This not only made it possible to construct a series of high voltage/energy density aqueous LIBs with unprecedented safety, but also brought high flexibility and even "open configurations" that have been hitherto unavailable for any LIB chemistries. While this new class of aqueous electrolytes has been successfully demonstrated to support diversified battery chemistries, the chemistry and formation mechanism of the key component, an aqueous SEI, has remained virtually unknown. In this work, combining various spectroscopic, electrochemical and computational techniques, we rigorously examined this new interphase, and comprehensively characterized its chemical composition, microstructure and stability in battery environment. A dynamic picture obtained reveals how a dense and protective interphase forms on anode surface under competitive decompositions of salt anion, dissolved ambient gases and water molecule. By establishing basic laws governing the successful formation of an aqueous SEI, the in-depth understanding presented in this work will assist the efforts in tailor-designing better interphases that enable more energetic chemistries operating farther away from equilibria in aqueous media.

Graphene oxide/MnO{sub 2} nanocomposite as destructive adsorbent of nerve-agent simulants in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Šťastný, Martin, E-mail: stastny@iic.cas.cz [Materials Chemistry Department, Institute of Inorganic Chemistry AS CR v.v.i., 25068 Husinec-Řež (Czech Republic); Faculty of the Environment, J.E. Purkyně University in Ústí nad Labem, Králova Výšina 7, 400 96 Ústí nad Labem (Czech Republic); Tolasz, Jakub; Štengl, Václav; Henych, Jiří [Materials Chemistry Department, Institute of Inorganic Chemistry AS CR v.v.i., 25068 Husinec-Řež (Czech Republic); Žižka, David [Faculty of the Environment, J.E. Purkyně University in Ústí nad Labem, Králova Výšina 7, 400 96 Ústí nad Labem (Czech Republic)

2017-08-01

Highlights: • Nanocomposite graphene oxide-birnessite-type MnO{sub 2} was synthesized by thermal hydrolysis. • New destructive sorbent for safe degradation of nerve-agent simulants. • 95% degradation activity for DMMP and TEP. - Abstract: Graphene oxide/MnO{sub 2} nanocomposite was prepared by thermal hydrolysis of potassium permanganate (KMnO{sub 4}) and 2-chloroacetamide aqueous solutions with graphene oxide (GO) suspension. The synthesized samples were characterized by specific surface area (BET) and porosity determination (BJH), X-ray Diffraction (XRD) and high-resolution electron microscopes (HRSEM, HRTEM). These nanocomposites were used in an experimental evaluation of their adsorption activity with nerve agent simulants dimethyl methyl phosphonate (DMMP) and triethyl phosphate (TEP) in aqueous media. The nanocomposites exhibited enhanced adsorptive degradation ability compared to pure manganese oxide (MnO{sub 2}) and GO. The GO amount in the nanocomposites affected their degradation activity substantially. The best adsorption efficiency was observed for samples with moderate GO amount. Three methods were used to observe the mechanism of the nerve-agent simulants deactivation: Gas chromatography with mass spectrometry (GC–MS), High-Performance Liquid Chromatography (HPLC) and in situ Infrared spectroscopy (FTIR). It was shown that the hydrolysis on the surface of prepared nanocomposites yields volatile primary alcohols (methanol and ethanol) as the main hydrolysis products.

Near-infrared chemodosimetric probes based on heptamethine cyanine dyes for the “naked-eye” detection of cyanide in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Qiu, Dali [College of Chemistry, Xiangtan University, Xiangtan 411105, Hunan Province (China); Liu, Yijiang, E-mail: liuyijiang84@iccas.ac.cn [College of Chemistry, Xiangtan University, Xiangtan 411105, Hunan Province (China); Li, Mengnan [State Key Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190 (China); Chen, Hongbiao, E-mail: chhb606@163.com [College of Chemistry, Xiangtan University, Xiangtan 411105, Hunan Province (China); Li, Huaming [College of Chemistry, Xiangtan University, Xiangtan 411105, Hunan Province (China)

2017-05-15

Two simple chemodosimetric probes (P1 and P2) based on heptamethine cyanine dyes have been synthesized for highly sensitive and selective detection of cyanide anions (CN{sup −}) in aqueous media. The probes with an immobilized indolium salt as the specifically nucleophilic addition reaction site for CN{sup −} exhibit absorption bands in the near-infrared (NIR) region (650–850 nm). Upon the addition of CN{sup −}, the probes display a blue-shifted spectrum and result in apparent color change from green to brilliant yellow that can be easily observed by the naked eye even in the presence of other interfering anions such as F{sup −}, AcO{sup −}, Br{sup −}, NO{sub 2}{sup −}, Cl{sup −}, SO{sub 4}{sup 2−} and I{sup −}. There are good linear relationships between the fluorescence intensity of the probes and CN{sup −} concentrations, and the detection limits for P1 and P2 are estimated to be 0.017 μM and 0.2 μM, respectively. The sensing mechanism of the nucleophilic addition is confirmed by {sup 1}H NMR and mass spectroscopic analysis. In addition, the probe P2 is employed for cell imaging and the detection of CN{sup −} in living cells L929 is successfully realized. - Graphical abstract: Simple chemodosimetric probes based on heptamethine cyanine dye were synthesized and applied to detect CN{sup −} in aqueous media with colorimetric and fluorescent dual channel recognition.

An Efficient and Practical Process for Pd/Cu Cocatalyzed Homocoupling Reaction of Terminal Alkynes Using Sodium Percarbonate as a Dual Reagent in Aqueous Media

Institute of Scientific and Technical Information of China (English)

ZHOU, Lei; ZHAN, Hai-Ying; LIU, Hai-Ling; JIANG, Huan-Feng

2007-01-01

A new process for the Pd/Cu co-catalyzed homocoupling reaction of terminal alkynes was developed. The reaction was carried out in aqueous media with sodium percarbonate as both a clean oxidant and a base. Meanwhile, a palladium complex immobilized on a synthetic PS-PEG400-PPh2 resin was used as the catalyst, which may be recovered by simple filtration and reused for several times with high activity.

Enhanced defluoridation capacity from aqueous media via hydroxyapatite decorated with carbon nanotube

Science.gov (United States)

Tang, Qingzi; Duan, Tongdan; Li, Peng; Zhang, Ping; Wu, Daishe

2018-04-01

In this work, the potential of a novel carbon nanotube-doped hydroxyapatite composite (CNT-HAP) for fluoride removal was investigated. The synthesized CNT-HAP composite was systematically characterized by X-ray diffraction(XRD), Fourier Transform infrared spectroscopy(FTIR), scanning electron microscope (SEM) and Brunauer–Emmett–Teller(BET). Batch adsorption experiments were conducted to investigate the defluorination capacity of CNT-HAP. The CNT-HAP composite has a maximum adsorption capacity of 11.05 mg·g-1 for fluoride, and the isothermal adsorption data were fitted by the Freundlich model to calculate the thermodynamic parameters. Thermodynamic analysis implies that the adsorption of fluoride on CNT-HAP is a spontaneous process. Furthermore, the adsorption of fluoride follows pseudo-second-order model. The effects of solution pH, co-existing anions and reaction temperature on defluorination efficiency were examined to optimize the operation conditions for fluoride adsorption. It is found that the optimized pH value for fluoride removal by CNT-HAP composite is 6. In addition, among five common anions studied in this work, the presence of HCO3- and PO43- could considerably affect the fluoride removal by CNT-HPA in aqueous media. Finally, the underlying mechanism for the fluoride removal by CNT-HAP is analysed, and an anion exchange process is proposed.

Synthesis and self-assembling of responsive polysaccharide-based copolymers in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Marques, Nivia do N.; Balaban, Rosangela de C. [Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN (Brazil); Halila, Sami; Borsali, Redouane, E-mail: borsali@cermav.cnrs.fr, E-mail: halila@cermav.cnrs.fr [Centre de Recherche sur les Macromolecules Vegetales (CERMAV), Grenoble (France)

2015-07-01

This work reports the synthesis and the thermoresponsive self-assembly behavior of carboxymethylcellulose-g-JeffamineM2070 and carboxymethylcellulose-g-JeffamineM600 copolymers in aqueous media. They were prepared through the grafting of two different types of amino-terminated poly(ethylene oxide-co-propylene oxide) chains onto the carboxylate groups of carboxymethylcellulose, by using water-soluble carbodiimide derivative and N-hydroxysuccinimide as coupling reagents. The grafting efficiency was confirmed by infrared and the degree of substitution by {sup 1}H NMR integrations. The salt effect on cloud point temperature was evaluated into different solvents (Milli-Q water, 0.5M NaCl, synthetic sea water (SSW) and 0.5M K{sub 2}CO{sub 3}) by UV-Vis and dynamic light scattering (DLS) measurements. Both copolymers showed lower cloud point temperature in 0.5M K2CO3 than in 0.5M NaCl and in SSW, which was attributed to the higher ionic strength for K{sub 2}CO{sub 3} combined to the ability of CO{sub 3}{sup 2-} to decrease polymer-water interactions. Copolymers chains displayed higher hydrodynamic radii than CMC precursor at 25 and 60 °C in saline solutions, and self-associations changed as a function of the environment and copolymer composition. (author)

Synthesis and self-assembling of responsive polysaccharide-based copolymers in aqueous media

International Nuclear Information System (INIS)

Marques, Nivia do N.; Balaban, Rosangela de C.; Halila, Sami; Borsali, Redouane

2015-01-01

This work reports the synthesis and the thermoresponsive self-assembly behavior of carboxymethylcellulose-g-JeffamineM2070 and carboxymethylcellulose-g-JeffamineM600 copolymers in aqueous media. They were prepared through the grafting of two different types of amino-terminated poly(ethylene oxide-co-propylene oxide) chains onto the carboxylate groups of carboxymethylcellulose, by using water-soluble carbodiimide derivative and N-hydroxysuccinimide as coupling reagents. The grafting efficiency was confirmed by infrared and the degree of substitution by "1H NMR integrations. The salt effect on cloud point temperature was evaluated into different solvents (Milli-Q water, 0.5M NaCl, synthetic sea water (SSW) and 0.5M K_2CO_3) by UV-Vis and dynamic light scattering (DLS) measurements. Both copolymers showed lower cloud point temperature in 0.5M K2CO3 than in 0.5M NaCl and in SSW, which was attributed to the higher ionic strength for K_2CO_3 combined to the ability of CO_3"2"- to decrease polymer-water interactions. Copolymers chains displayed higher hydrodynamic radii than CMC precursor at 25 and 60 °C in saline solutions, and self-associations changed as a function of the environment and copolymer composition. (author)

Effectively designed molecularly imprinted polymers for selective isolation of the antidiabetic drug metformin and its transformation product guanylurea from aqueous media

Energy Technology Data Exchange (ETDEWEB)

Kyzas, George Z.; Nanaki, Stavroula G. [Laboratory of Polymer Chemistry and Technology, Department of Chemistry, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki (Greece); Koltsakidou, Anastasia; Papageorgiou, Myrsini; Kechagia, Maria [Laboratory of Environmental Pollution Control, Department of Chemistry, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki (Greece); Bikiaris, Dimitrios N. [Laboratory of Polymer Chemistry and Technology, Department of Chemistry, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki (Greece); Lambropoulou, Dimitra A., E-mail: dlambro@chem.auth.gr [Laboratory of Environmental Pollution Control, Department of Chemistry, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki (Greece)

2015-03-25

Highlights: • Preparation of novel MIPs with remarkable recognition properties. • Selective isolation and removal of metformin and guanylurea from aqueous media. • Detailed adsorbent characterization and adsorption studies. • Successful application of synthesized MIPs as dispersive SPE sorbents. • Estimation of expanded uncertainty following a bottom-up approach. - Abstract: In the present study, two novel molecularly imprinted polymers (MIPs) with remarkable recognition properties for metformin and its transformation product, guanylurea, have been prepared for their selective, enrichment, isolation and removal from aqueous media. The prepared adsorbents were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and swelling experiments. The performance of the prepared MIPs was evaluated by various parameters including the influence of pH, contact time, temperature and initial compound concentration. The effects on the adsorption behavior of the removal process parameters were studied and the equilibrium data were fitted by the Langmuir and Freundlich models. Due to the imprinting effect, adsorption performance of MIPs was always superior to its corresponding NIP (non-imprinted polymer), with maximum adsorption capacity ∼80 mg g{sup −1} for both MIPs. Stability and reusability of the MIPs up to the 5th cycle meant that they could be applied repeatedly without losing substantial removal ability. In the next step, the prepared MIP nanoparticles were evaluated as sorbents in a dispersive solid phase extraction (D-SPE) configuration for selective enrichment and determination of metformin and guanylurea in different aqueous matrices. Under the working extraction conditions, the D-SPE method showed good linearity in the range of 50–1000 ng L{sup −1}, repeatability of the extractions (RSD 2.1–5.1%, n = 3), and low limits of detection (1.5–3.4 ng L{sup −1}). The expanded uncertainty of the data obtained

Benchmarking uranyl peroxide capsule chemistry in organic media

Energy Technology Data Exchange (ETDEWEB)

Neal, Harrison A.; Nyman, May [Department of Chemistry, Oregon State University, Corvallis, OR (United States); Szymanowski, Jennifer; Fein, Jeremy B.; Burns, Peter C. [Department of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, Notre Dame, IN (United States)

2017-01-03

Uranyl peroxide capsules are a recent addition to polyoxometalate (POM) chemistry. Ten years of development has ensued only in water, while transition metal POMs are commonly exploited in aqueous and organic media, controlled by counterions or ligation to render the clusters hydrophilic or hydrophobic. Here, new uranyl POM behavior is recognized in organic media, including (1) stabilization and immobilization of encapsulated hydrophilic countercations, identified by Li nuclear magnetic resonance (NMR) spectroscopy, (2) formation of new cluster species upon phase transfer, (3) extraction of uranyl clusters from different starting materials including simulated spent nuclear fuel, (4) selective phase transfer of one cluster type from a mixture, and (5) phase transfer of clusters from both acidic and alkaline media. The capsule morphology of the uranyl POMs renders accurate characterization by X-ray scattering, including the distinction of geometrically similar clusters. Compositional analysis of the aqueous phase post-extraction provided a quantitative determination of the ion exchange process that enables transfer of the clusters into the organic phase. Preferential partitioning of uranyl POMs into organic media presents new frontiers in metal ion behavior and chemical reactions in the confined space of the cluster capsules in hydrophobic media, as well as the reactivity of clusters at the organic/aqueous interface. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Benchmarking uranyl peroxide capsule chemistry in organic media

International Nuclear Information System (INIS)

Neal, Harrison A.; Nyman, May; Szymanowski, Jennifer; Fein, Jeremy B.; Burns, Peter C.

2017-01-01

Uranyl peroxide capsules are a recent addition to polyoxometalate (POM) chemistry. Ten years of development has ensued only in water, while transition metal POMs are commonly exploited in aqueous and organic media, controlled by counterions or ligation to render the clusters hydrophilic or hydrophobic. Here, new uranyl POM behavior is recognized in organic media, including (1) stabilization and immobilization of encapsulated hydrophilic countercations, identified by Li nuclear magnetic resonance (NMR) spectroscopy, (2) formation of new cluster species upon phase transfer, (3) extraction of uranyl clusters from different starting materials including simulated spent nuclear fuel, (4) selective phase transfer of one cluster type from a mixture, and (5) phase transfer of clusters from both acidic and alkaline media. The capsule morphology of the uranyl POMs renders accurate characterization by X-ray scattering, including the distinction of geometrically similar clusters. Compositional analysis of the aqueous phase post-extraction provided a quantitative determination of the ion exchange process that enables transfer of the clusters into the organic phase. Preferential partitioning of uranyl POMs into organic media presents new frontiers in metal ion behavior and chemical reactions in the confined space of the cluster capsules in hydrophobic media, as well as the reactivity of clusters at the organic/aqueous interface. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Enhanced dispersion of boron nitride nanosheets in aqueous media by using bile acid-based surfactants

Science.gov (United States)

Chae, Ari; Park, Soo-Jin; Min, Byunggak; In, Insik

2018-01-01

Facile noncovalent surface functionalization of hydroxylated boron nitride nanosheet (BNNS-OH) was attempted through the sonication-assisted exfoliation of h-BN in aqueous media in the presence of bile acid-based surfactants such as sodium cholic acid (SC) or sodium deoxycholic acid (SDC), resulting in SC- or SDC-BNNS-OH dispersion with high up to 2 mg ml-1 and enhanced dispersion stability due to the increased negative zeta potential. While prepared SC-BNNS-OH revealed multi-layered BNNS structures, the large lateral sizes of hundreds nanometers and clear h-BN lattice structures are very promising for the preparation and application of water-processable BNNS-based nanomaterials. It is regarded that noncovalent functionalization of BNNS-OH based on σ-π interaction between with σ-rich bile acid-based amphiphiles and π-rich BNNS is very effective to formulate multi-functional BNNS-based nanomaterials or hybrids that can be utilized in various applications where both the pristine properties of BNNS and the extra functions are simultaneously required.

Arenediazonium salts transformations in water media: Coming round to origins

OpenAIRE

Marina E. Trusova; Ksenia V. Kutonova; Victor V. Kurtukov; Victor D. Filimonov; Pavel S. Postnikov

2016-01-01

Aromatic diazonium salts belong to an important class of organic compounds. The chemistry of these compounds has been originally developed in aqueous media, but then chemists focused on new synthetic methods that utilize reactions of diazonium salts in organic solvents. However, according to the principles of green chemistry and resource-efficient technologies, the use of organic solvents should be avoided. This review summarizes new trends of diazonium chemistry in aqueous media that satisfy...

DETERMINATION OF KINETICS OF DEGRADATION AND MOBILITY OF DITHIOCARBAMATES FUNGICIDES IN AQUEOUS MEDIA AND IN MOROCCAN SOIL

Directory of Open Access Journals (Sweden)

Said El Antri

2010-07-01

Full Text Available Contribution analysis of dithiocarbamates pesticides used on tomatoes treatment has been reported. The study is focused on analysis and determination of some dithiocarbamates like, Maneb, Mancozeb, Zineb and Propineb, in order to achieve accurate impact of theses pesticides on water and soil. Analysis method is based on decomposition of dithiocarbamate by heating under acidic attack to give carbon disulfide complexed with copper acetate solution in presence of diethanolamine. Complex formed is dosed spectrophotometrically at 435 nm. Degradation kinetic of dithiocarbamate in aqueous media have been realized and proved that dithiocarbamate are degraded by simple air exposition. In the other hand, pH affects also dithiocarbamate degradation by increasing hydroxyl ions to participate for dithiocarbamate instability. Dithiocarbamate mobility on Moroccan soils samples have been realised and don’t have the same degradation mode.

LASERS, ACTIVE MEDIA: The aqueous-polyelectrolyte dye solution as an active laser medium

Science.gov (United States)

Akimov, A. I.; Saletskii, A. M.

2000-11-01

The spectral, luminescent, and lasing properties of aqueous solutions of a cationic dye rhodamine 6G with additions of anion polyelectrolytes — polyacrylic and polymethacrylic acids — are studied. It is found that the energy and spectral properties of lasing of these solutions depend on the ratio of concentrations of polyelectrolyte and molecules. It is also found that the lasing parameters of aqueous-polyelectrolyte dye solutions can be controlled by changing the structure of the molecular system. The variation in the structure of aqueous-polyelectrolyte dye solutions of rhodamine 6G resulted in an almost five-fold increase in the lasing efficiency compared to that in aqueous dye solutions.

Functional polyaniline/multiwalled carbon nanotube composite as an efficient adsorbent material for removing pharmaceuticals from aqueous media.

Science.gov (United States)

Dutra, Flávia Viana Avelar; Pires, Bruna Carneiro; Nascimento, Tienne Aparecida; Borges, Keyller Bastos

2018-09-01

The composite polyaniline/multiwalled carbon nanotube (PAni/MWCNT, 1:0.1 w/w) was developed with the intention of binding the adsorbent properties of two materials and using it to adsorb pharmaceuticals from aqueous media. PAni/MWCNT was characterized by scanning electron microscopy, thermogravimetry, infrared spectroscopy, pH at the point of zero charge, and the effect on the surface wettability of the material. As proof of concept, adsorption studies were carried out using meloxicam (MLX) as the pharmaceutical and it was evaluated as a function of pH, temperature, ionic strength, contact time and variation in concentration. Kinetics and isothermal models were applied to evaluate the mechanism of the adsorption process. The best MLX adsorption result was at pH 2 with 6 min of contact with PAni/MWCNT. The kinetics models that fitted the experimental data were pseudo-second order and Elovich and the kinetics model was the dual-site Langmuir-Freundlich. Both models suggest that the adsorption occurs by the chemical nature of the surface and in the pores of the energetically heterogeneous composite. The PAni/MWCNT presented an adsorption capacity of 221.2 mg g -1 , a very good value when compared with the literature and can be used to remove pharmaceuticals from aqueous environments. Copyright © 2018 Elsevier Ltd. All rights reserved.

A cyclo olefin polymer microfluidic chip with integrated gold microelectrodes for aqueous ans non-aqueous electrochemistry

DEFF Research Database (Denmark)

Illa, Xavi; Sala, Olga Ordeig; Snakenborg, Detlef

2010-01-01

and 24 m deep channel was fabricated via hot embossing. Cyclic voltammetric measurements were carried out in aqueous and organic media, using a solution consisting of 5 mM ferrocyanide/ferricyanide in 0.5 M KNO3 and 5 mM ferrocene in 0.1 M TBAP/acetonitrile, respectively. Experimental currents obtained...

Investigation of the mechanisms of using metal complexation and cellulose nanofiber/sodium alginate layer-by-layer coating for retaining anthocyanin pigments in thermally processed blueberries in aqueous media.

Science.gov (United States)

Jung, Jooyeoun; Cavender, George; Simonsen, John; Zhao, Yanyun

2015-03-25

This study investigated the mechanisms of anthocyanin pigment retention using Fe(3+)-anthocyanin complexation and cellulose nanofiber (CNF)/sodium alginate (SA) layer-by-layer (LBL) coatings on thermally processed blueberries in aqueous media. Anthocyanin pigments were polymerized through complexation with Fe(3+) but readily degraded by heat (93 °C for 7 min) in the aqueous media because of poor stability. CNF/SA LBL coating was successful to retain anthocyanin pigments in thermally processed blueberries. Fruits coated with CNF containing CaCl2 followed by treatment in a SA bath formed a second hydrogel layer onto the CNF layer (LBL coating system) through cross-linking between Ca(2+) and alginic acid. Methyl-cellulose-modified CNF improved the interactions between CNF, the fruit surface, and the SA layer. This study demonstrated that the CNF/SA LBL coating system was effective to retain anthocyanin pigments on thermally processed whole blueberries, whereas no combined benefit of complexation with coating was observed. Results explained the mechanisms of the new approaches for developing colorful and nutritionally enhanced anthocyanin-rich fruit products.

Development of a pH-responsive imprinted polymer for diclofenac and study of its binding properties in organic and aqueous media.

Science.gov (United States)

Mohajeri, Seyed Ahmad; Malaekeh-Nikouei, Bizhan; Sadegh, Hasan

2012-05-01

Three different molecularly imprinted polymers (MIPs) for drug delivery of diclofenac in gastrointestinal tract were synthesized employing bulk polymerization method and their binding and release properties were studied in different pH values. Methacrylic acid (MAA), methacrylamide (MAAM) and 4-vinyl pyridine (4VP) were tested as functional monomers and ethylene glycole dimethacrylate (EDMA) was used as a cross-linker monomer in polymeric feed. Binding properties and imprinting factor (IF) of MIPs were studied in comparison with their non-imprinted ones (Blank) in organic and aqueous media. Diclofenac release in aqueous solvents at pH values of 1.5, 6.0 and 8.0, simulating gastrointestinal fluids, were also studied. The results indicated the specific binding of diclofenac to imprinted polymers. Duo to the stronger non-specific bounds in aqueous solutions, IF values decreased in water compared to acetonitrile as an organic medium. Our results proved that all polymers represented pH-responsive diclofenac delivery at above conditions. The data showed that imprinted polymer, prepared by MAA had superior properties, in comparison with other polymers, for minimum release (14%) of drug in gastric acid and maximum release (90%) in basic condition. The results indicated that diclofenac imprinted polymer could be used as a pH-responsive matrix in preparation of a new drug delivery system for diclofenac.

Electrochemical behavior of uranyl in anhydrous polar organic media

Energy Technology Data Exchange (ETDEWEB)

Burn, Adam G.; Nash, Kenneth L. [Washington State Univ., Pullmann, WA (United States). Dept. of Chemistry

2017-09-01

Weak complexes between pentavalent and hexavalent actinyl cations have been reported to exist in acidic, non-complexing high ionic strength aqueous media. Such ''cation-cation complexes'' were first identified in the context of actinide-actinide redox reactions in acidic aqueous media relevant to solvent extraction-based separation systems, hence their characterization is of potential interest for advanced nuclear fuel reprocessing. This chemistry could be relevant to efforts to develop advanced actinide separations based on the upper oxidation states of americium, which are of current interest. In the present study, the chemical behavior of pentavalent uranyl was examined in non-aqueous, aprotic polar organic solvents (propylene carbonate and acetonitrile) to determine whether UO{sub 2}{sup +} cations generated at the reducing working electrode surface would interact with the UO{sub 2}{sup 2+} cations in the bulk phase to form cation-cation complexes in such media. In magnesium perchlorate media, the electrolyte adsorbed onto the working electrode surface and interfered with the uranyl reduction/diffusion process through an ECE (electron transfer/chemical reaction/electron transfer) mechanism. In parallel studies of uranyl redox behavior in tetrabutylammonium hexafluorophosphate solutions, an EC (electron transfer/chemical reaction) mechanism was observed in the cyclic voltammograms. Ultimately, no conclusive electrochemical evidence demonstrated uranyl cation-cation interactions in the non-aqueous, aprotic polar organic solvent solutions, though the results reported do not completely rule out the presence of UO{sub 2}{sup +}.UO{sub 2}{sup 2+} complexes.

REMOVAL OF LEAD(II) IONS FROM AQUEOUS SOLUTIONS ...

African Journals Online (AJOL)

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lung cancer, convulsion and even death if ingested at elevated levels. ... osmosis have been used for removing heavy metal ions from aqueous media [4-6]. ... organic molecules and silica surface functions, (ii) chlorination of the silica surface ...

Enzyme Stability and Activity in Non-Aqueous Reaction Systems: A Mini Review

Directory of Open Access Journals (Sweden)

Shihui Wang

2016-02-01

Full Text Available Enormous interest in biocatalysis in non-aqueous phase has recently been triggered due to the merits of good enantioselectivity, reverse thermodynamic equilibrium, and no water-dependent side reactions. It has been demonstrated that enzyme has high activity and stability in non-aqueous media, and the variation of enzyme activity is attributed to its conformational modifications. This review comprehensively addresses the stability and activity of the intact enzymes in various non-aqueous systems, such as organic solvents, ionic liquids, sub-/super-critical fluids and their combined mixtures. It has been revealed that critical factors such as Log P, functional groups and the molecular structures of the solvents define the microenvironment surrounding the enzyme molecule and affect enzyme tertiary and secondary structure, influencing enzyme catalytic properties. Therefore, it is of high importance for biocatalysis in non-aqueous media to elucidate the links between the microenvironment surrounding enzyme surface and its stability and activity. In fact, a better understanding of the correlation between different non-aqueous environments and enzyme structure, stability and activity can contribute to identifying the most suitable reaction medium for a given biotransformation.

Moessbauer spectroscopy characterization and electrochemical study of the kinetics of oxidation of iron in chlorinated aqueous media: structure and equilibrium diagram of green rust one

International Nuclear Information System (INIS)

Genin, J.M.R.; Rezel, D.; Bauer, Ph.; Olowe, A.; Beral, A.

1986-01-01

Moessbauer spectroscopy allows to precise the structure of akaganeite, lepidocrocite, green rust I and initial hydroxide of a simulated corrosion process of iron in chlorinated aqueous media. The characterization of the compounds during the process is coupled with E - pH recordings, yielding the kinetics of the various reactions (order and activation energy) as well as the Pourbaix diagram of Green Rust I by scanning the [Cl - ]/[OH - ] ratio. (author) 16 refs., 15 figs

Spectral behaviour of eosin Y in different solvents and aqueous surfactant media

Science.gov (United States)

Chakraborty, Moumita; Panda, Amiya Kumar

2011-10-01

Photophysical behaviour of the anionic xanthene dye, eosin Y (EY) was investigated in solvents of different polarities as well as in the presence of aqueous cationic surfactants. From the correlation between ET(30) and Kosower Z values of EY in different solvents, subsequent parameters for EY were determined in the presence of surfactants. A red shift, both in the absorption and emission spectra of EY, was observed with decreasing solvent polarity. Dimerisation of EY was found to be dependent on solvent polarity. Cationic surfactants retarded the process of dimerisation, which were evident from the lower dimerisation constant ( KD) values, compared to that of in pure water. Dye-surfactant interaction constants were determined at different temperatures (298-318 K) and subsequently the thermodynamic parameters, viz., Δ G°, Δ H° and Δ S° were evaluated using the interaction constant values. The fluorescence spectra of EY followed the same trend as in the absorption spectra, although with lesser extents. Stokes shifts were calculated and correlated with the polarity of the medium. Fluorescence of EY was initially quenched by the cationic surfactants in their pre-micellar region, which then followed a red shift with intensity enhancement. Fluorescence quenching was found to be of Stern-Volmer type where the excited state lifetime of EY remained unchanged in different surfactant media. However, the anisotropy value of EY was changed in the post micellar region of surfactants.

Assembly of DNA Architectures in a Non-Aqueous Solution

Directory of Open Access Journals (Sweden)

Thomas J. Proctor

2012-08-01

Full Text Available In the present work, the procedures for the creation of self-assembled DNA nanostructures in aqueous and non-aqueous media are described. DNA-Surfactant complex formation renders the DNA soluble in organic solvents offering an exciting way to bridge the transition of DNA origami materials electronics applications. The DNA retains its structural features, and these unique geometries provide an interesting candidate for future electronics and nanofabrication applications with potential for new properties. The DNA architectures were first assembled under aqueous conditions, and then characterized in solution (using circular dichroism (CD spectroscopy and on the surface (using atomic force microscopy (AFM. Following aqueous assembly, the DNA nanostructures were transitioned to a non-aqueous environment, where butanol was chosen for optical compatibility and thermal properties. The retention of DNA hierarchical structure and thermal stability in non-aqueous conditions were confirmed via CD spectroscopy. The formation and characterization of these higher order DNA-surfactant complexes is described in this paper.

Organic Reactions in Aqueous Media (by Chao-Jun Li and Tak-Hang Chan)

Science.gov (United States)

Rosan, Reviewed Alan M.

2000-06-01

This concise book joins the series of Wiley Interscience special topic publications. In seven chapters it selectively reviews the burgeoning literature on organic reactions conducted in water or in aqueous media as a reaction cosolvent, nicely complementing another recent book on the subject by Grieco. Following a short introduction there are six chapters that vary in length from 10 to 50 pages; they cover pericyclic reactions, nucleophilic additions and substitutions, metal-mediated reactions, transition metal-catalyzed reactions, oxidation and reduction reactions, and industrial applications. These chapters, each of which is prefaced with a short provocative quotation, also vary in depth, containing from 11 to more than 180 references. The literature is complete through 1996 and commendably includes citations of original papers by Barbier, Faraday, Frankland, Grignard, Kolbe, Lapworth, and Reformatsky as well as references to selected U.S. and foreign patents and the Russian literature. There is a subject index but no author index. This book is timely and effective. From the title, one might expect a broad discussion of the unique properties of water and water-soluble components (salts, surfactants, etc.) that would be thought to bear on organic reactivity. The first chapter opens by noting that water is the most abundant volatile material in comets and briefly describes those properties that suggest its utility as a solvent or cosolvent, summarizing the potential technical, economic, and environmental advantages. Also described are the remarkable changes in density, conductance, heat capacity, dielectric constant, and ionization constant that accompany the transition to the critical point, but the emphasis here is on the effect of water under non-critical conditions. Discussion of the structure of liquid water and the role of hydrogen bonding in mediating molecular recognition events is abbreviated. In fact, the term "hydrogen bond" is surprisingly absent from

Enzymes from solvent-tolerant microbes: useful biocatalysts for non-aqueous enzymology.

Science.gov (United States)

Gupta, Anshu; Khare, S K

2009-01-01

Solvent-tolerant microbes are a newly emerging class that possesses the unique ability to thrive in the presence of organic solvents. Their enzymes adapted to mediate cellular and metabolic processes in a solvent-rich environment and are logically stable in the presence of organic solvents. Enzyme catalysis in non-aqueous/low-water media is finding increasing applications for the synthesis of industrially important products, namely peptides, esters, and other trans-esterification products. Solvent stability, however, remains a prerequisite for employing enzymes in non-aqueous systems. Enzymes, in general, get inactivated or give very low rates of reaction in non-aqueous media. Thus, early efforts, and even some recent ones, have aimed at stabilization of enzymes in organic media by immobilization, surface modifications, mutagenesis, and protein engineering. Enzymes from solvent-tolerant microbes appear to be the choicest source for studying solvent-stable enzymes because of their unique ability to survive in the presence of a range of organic solvents. These bacteria circumvent the solvent's toxic effects by virtue of various adaptations, e.g. at the level of the cytoplasmic membrane, by degradation and transformation of solvents, and by active excretion of solvents. The recent screening of these exotic microbes has generated some naturally solvent-stable proteases, lipases, cholesterol oxidase, cholesterol esterase, cyclodextrin glucanotransferase, and other important enzymes. The unique properties of these novel biocatalysts have great potential for applications in non-aqueous enzymology for a range of industrial processes.

Chemical systems in aqueous solutions for using in the holographic ionizing radiation

International Nuclear Information System (INIS)

Nicolau-Rebigan, S.

1979-01-01

Some types of chemical systems in aqueous solutions for utilization as active media in holographic ionizing radiation dosimeter are presented. One discussed some advantages of the holographic dosimeter comparatively with another existing types. It is outlined the advantages of using aqueousss solutions as active media in holographic dosimeter. (author)

SINTESIS DAN MODIFIKASI LAPIS TIPIS KITOSAN-TRIPOLIFOSFAT

Directory of Open Access Journals (Sweden)

M Alauhdin

2014-11-01

Full Text Available Dalam bidang medis, kitosan telah banyak digunakan yakni pada sistem penghantaran dan pelepasan obat. Pelepasan obat dengan kitosan memiliki keterbatasan karena kitosan cepat sekali menyerap air dan memiliki derajat swelling yang tinggi sehingga menyebabkan pelepasan obat terjadi dengan cepat. Diharapkan dengan memodifikasi struktur kitosan secara kimia dapat meningkatan kelarutannya dalam pelarut-pelarut organik. Telah dilakukan sintesis dan modifikasi lapis tipis kitosan. Modifikasi dilakukan melalui pembentukan ikatan silang kitosan dengan tripolifosfat (TPP pada kondisi asam untuk menghasilkan kitosan-TPP. Ikatan silang yang terbentuk diamati dengan FTIR. Sementara itu, pengaruh hasil pengikatan silang diamati dengan membandingkan rasio swelling kitosan-TPP pada kondisi pH yang berbeda-beda. Rasio swelling lapis tipis cenderung konstan setelah terjadi pengikatan silang kitosan dengan tripolifosfat. Reaksi tripolifosfat dengan kitosan melalui pembentukan ikatan silang menjadikan lapis tipis semakin rapat sehingga molekul air sulit untuk berdifusi masuk ke dalam struktur kitosan-tripolifosfat. Hasil ini menunjukkan bahwa pengikatan silang mampu mengurangi kelarutan dan meningkatkan sifat mekanik kitosan. Rasio swelling lapis tipis berkurang dengan adanya pengikatan silang. Hal ini mengindikasikan bahwa pengikatan silang oleh TPP dapat mengurangi hidrofilitas lapis tipis karena gugus amino yang reaktif telah bereaksi dengan ion tripolifosfat. In the medical field, chitosan has been widely used in the delivery systems and drug release. Drug release with chitosan has limitations because chitosan absorbs water very quickly and have a high degree of swelling that causes the release of the drug occurs rapidly. It is expected that by modifying the chemical structure of chitosan could improve its solubility in organic solvents. The synthesis and modification of chitosan thin film have been done. It was performed through the formation of crosslinked

Removal of Cd (II from Aqueous Media by Adsorption onto Chemically and Thermally Treated Rice Husk

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María Camila Hoyos-Sánchez

2017-01-01

Full Text Available Chemically and thermally treated rice husks were evaluated as a potential decontaminant of toxic Cd (II in aqueous media. Rice husk (RH, a by-product from rice milling, was chemically treated with HCl and NaOH. Then, thermal treatments to 300, 500, and 700°C were applied. The chemical composition and morphological characteristics of RH were evaluated by different techniques. The specific surface area analysis of RH samples by BET nitrogen adsorption method provided specific surface areas ranging from 6 to 14 m2/g. SEM, FTIR, and EDX analyses of RH were carried out to determine the surface morphology, functional groups involved in metal binding mechanism, and C/O and C/Si ratios, respectively. The maximum Cd (II adsorption capacity was 28.27 mg/g at an optimum pH, 6.0. The kinetic studies revealed that adsorption process followed the pseudo-second-order kinetic model.

Removal of nitrate, ammonia and phosphate from aqueous solutions in packed bed filter using biochar augmented sand media

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El Hanandeh Ali

2017-01-01

Full Text Available Nutrients from wastewater are a major source of pollution because they can cause significant impact on the ecosystem. Accordingly, it is important that the nutrient concentrations are kept to admissible levels to the receiving environment. Often regulatory limits are set on the maximum allowable concentrations in the effluent. Therefore, wastewater must be treated to meet safe levels of discharge. In this study, laboratory investigation of the efficiency of packed bed filters to remove nitrate, ammonium and phosphate from aqueous solutions were conducted. Sand and sand augmented with hydrochloric acid treated biochar (SBC were used as packing media. Synthetic wastewater solution was prepared with PO43−, NO3−, NH4+ concentrations 20, 10, 50 mg/L, respectively. Each experiment ran for a period of five days; samples from the effluent were collected on alternate days. All experiments were duplicated. Over the experiment period, the average removal efficiency of PO43−, NO3−, NH4+ were 99.2%, 72.9%, 96.7% in the sand packed columns and 99.2%, 82.3%, 97.4% in the SBC packed columns, respectively. Although, the presence of biochar in the packing media had little effect on phosphate and ammonium removal, it significantly improved nitrate removal.

DEVELOPMENT OF PROTOTYPE TITANATE ION EXCHANGE LOADED MEMBRANES FOR STRONTIUM, CESIUM AND ACTINIDE DECONTAMINATION FROM AQUEOUS MEDIA

Energy Technology Data Exchange (ETDEWEB)

Oji, L; Keisha Martin, K; David Hobbs, D

2008-05-30

We have successfully incorporated high surface area particles of titanate ion exchange materials (monosodium titanate and crystalline silicotitanate) with acceptable particle size distribution into porous and inert support membrane fibrils consisting of polytetrafluoroethylene (Teflon{reg_sign}), polyethylene and cellulose materials. The resulting membrane sheets, under laboratory conditions, were used to evaluate the removal of surrogate radioactive materials for cesium-137 and strontium-90 from high caustic nuclear waste simulants. These membrane supports met the nominal requirement for nonchemical interaction with the embedded ion exchange materials and were porous enough to allow sufficient liquid flow. Some of this 47-mm size stamped out prototype titanium impregnated ion exchange membrane discs was found to remove more than 96% of dissolved cesium-133 and strontium-88 from a caustic nuclear waste salt simulants. Since in traditional ion exchange based column technology monosodium titanate (MST) is known to have great affinity for the sorbing of other actinides like plutonium, neptunium and even uranium, we expect that the MST-based membranes developed here, although not directly evaluated for uptake of these three actinides because of costs associated with working with actinides which do not have 'true' experimental surrogates, would also show significant affinity for these actinides in aqueous media. It was also observed that crystalline silicotitanate impregnated polytetrafluoroethylene or polyethylene membranes became less selective and sorbed both cesium and strontium from the caustic aqueous salt simulants.

Cr(VI) adsorption on functionalized amorphous and mesoporous silica from aqueous and non-aqueous media

International Nuclear Information System (INIS)

Perez-Quintanilla, Damian; Hierro, Isabel del; Fajardo, Mariano; Sierra, Isabel

2007-01-01

A mesoporous silica (SBA-15) and amorphous silica (SG) have been chemically modified with 2-mercaptopyridine using the homogeneous route. This synthetic route involved the reaction of 2-mercaptopyridine with 3-chloropropyltriethoxysilane prior to immobilization on the support. The resulting material has been characterized by powder X-ray diffraction, nitrogen gas sorption, FT-IR and MAS NMR spectroscopy, thermogravimetry and elemental analysis. The solid was employed as a Cr(VI) adsorbent from aqueous and non-aqueous solutions at room temperature. The effect of several variables (stirring time, pH, metal concentration and solvent polarity) has been studied using the batch technique. The results indicate that under the optimum conditions, the maximum adsorption value for Cr(VI) was 1.83 ± 0.03 mmol/g for MP-SBA-15, whereas the adsorption capacity of the MP-SG was 0.86 ± 0.02 mmol/g. On the basis of these results, it can be concluded that it is possible to modify chemically SBA-15 and SG with 2-mercaptopyridine and to use the resulting modified silicas as effective adsorbents for Cr(VI)

Streaming: A Media Hydrography of Televisual Flows

Directory of Open Access Journals (Sweden)

Ghislain Thibault

2015-09-01

Full Text Available This paper focuses on the continuities, rather than the ruptures, between digital television and past media forms. It situates the metaphor of “streaming” in contrast to and connection with previous fluid metaphors that have been used to describe different models of media transmission. From the early use of aqueous vocabulary that shaped popular and scientific understandings of electricity transmission to the seminal studies of mass communication concerning the flows of information, images of fluidity have long shaped cultural understandings of the inner logics of media infrastructures. Building on the work of media archaeologist Erkki Huhtamo, I approach these metaphors as “recurrent topoi” in media culture.

Removal of Hexavalent Chromium from Aqueous Solutions using ...

African Journals Online (AJOL)

The hexavalent chromium exists in aquatic media as water soluble complex anions and persist. These are concentrated in industrial waste water especially from the tannery industries and release of effluents from industries adversely affects the environment. The removal of heavy metals from aqueous solutions is carried ...

Laboratory Experiments and Modeling of Pooled NAPL Dissolution in Porous Media

Science.gov (United States)

Copty, N. K.; Sarikurt, D. A.; Gokdemir, C.

2017-12-01

The dissolution of non-aqueous phase liquids (NAPLs) entrapped in porous media is commonly modeled at the continuum scale as the product of a chemical potential and an interphase mass transfer coefficient, the latter expressed in terms of Sherwood correlations that are related to flow and porous media properties. Because of the lack of precise estimates of the interface area separating the NAPL and aqueous phase, numerous studies have lumped the interfacial area into the interphase mass transfer coefficient. In this paper controlled dissolution experiments from a pooled NAPL were conducted. The immobile NAPL mass is placed at the bottom of a flow cell filled with porous media with water flowing on top. Effluent aqueous phase concentrations were measured for a wide range of aqueous phase velocities and for two types of porous media. To interpret the experimental results, a two-dimensional pore network model of the NAPL dissolution was developed. The well-defined geometry of the NAPL-water interface and the observed effluent concentrations were used to compute best-fit mass transfer coefficients and non-lumped Sherwood correlations. Comparing the concentrations predicted with the pore network model to simple previously used one-dimensional analytic solutions indicates that the analytic model which ignores the transverse dispersion can lead to over-estimation of the mass transfer coefficient. The predicted Sherwood correlations are also compared to previously published data and implications on NAPL remediation strategies are discussed.

Cast iron deterioration with time in various aqueous salt solutions

Indian Academy of Sciences (India)

Unknown

various aqueous salt solutions have been carried out using total immersion test ... circuit potential, Icorr, Tafel slopes, corrosion rate, have been calculated by standard methods. ..... Rao B V S 1980 in Maintenance for reliability (Bombay: Media.

Non-Enzymatic biopolymerization reactions supported by heterogeneous media

DEFF Research Database (Denmark)

Monnard, Pierre-Alain

2011-01-01

Heterogeneous media, such as micro-structured aqueous environments, could offer an alternative approach to the synthesis of biopolymers with novel functions. Structured media are here defined as specialized, self-assembled structures that are formed, e.g, by amphiphiles, such as liposomes, emulsion...... compartments and lipid-bilayer lattices. Another kind of media is represented by co-existing, self-assembled phases in the reaction medium, e.g., in water-ice matrices. These media have the capacity to assemble chemical molecules or complex catalytic assemblies into unique configurations that are unstable...

Lignin transformations and reactivity upon ozonation in aqueous media

Science.gov (United States)

Khudoshin, A. G.; Mitrofanova, A. N.; Lunin, V. V.

2012-03-01

The reaction of ozone with lignin in aqueous acidic solutions is investigated. The Danckwerst model is used to describe the kinetics of gas/liquid processes occurring in a bubble reactor. The efficient ozonation rate of a soluble lignin analog, sodium lignosulfate, is determined. The main lines of the reaction between ozone and lignin are revealed on the basis of kinetic analysis results and IR and UV spectroscopy data.

Modeling reactive geochemical transport of concentrated aqueous solutions in variably saturated media

Energy Technology Data Exchange (ETDEWEB)

Zhang, Guoxiang; Zheng, Zuoping; Wan, Jiamin

2004-01-28

Concentrated aqueous solutions (CAS) have unique thermodynamic and physical properties. Chemical components in CAS are incompletely dissociated, especially those containing divalent or polyvalent ions. The problem is further complicated by the interaction between CAS flow processes and the naturally heterogeneous sediments. As the CAS migrates through the porous media, the composition may be altered subject to fluid-rock interactions. To effectively model reactive transport of CAS, we must take into account ion-interaction. A combination of the Pitzer ion-interaction and the ion-association model would be an appropriate way to deal with multiple-component systems if the Pitzer' parameters and thermodynamic data of dissolved components and the related minerals are available. To quantify the complicated coupling of CAS flow and transport, as well as the involved chemical reactions in natural and engineered systems, we have substantially extended an existing reactive biogeochemical transport code, BIO-CORE{sup 2D}{copyright}, by incorporating a comprehensive Pitzer ion-interaction model. In the present paper, the model, and two test cases against measured data were briefly introduced. Finally we present an application to simulate a laboratory column experiment studying the leakage of the high alkaline waste fluid stored in Hanford (a site of the U.S. Department of Energy, located in Washington State, USA). With the Pitzer ion-interaction ionic activity model, our simulation captures measured pH evolution. The simulation indicates that all the reactions controlling the pH evolution, including cation exchanges, mineral precipitation and dissolution, are coupled.

SINTESIS FOSFOLIPID MENGANDUNG ASAM LEMAK w-3 DARI FOSFOLIPID KEDELAI DAN MINYAK KAYA ASAM LEMAK w-3 DARI HASIL SAMPING PENGALENGAN TUNA

Directory of Open Access Journals (Sweden)

Teti Estiasih

2013-03-01

Full Text Available Synthesis of Phospholipid Containing w-3 Fatty Acids from Soy Phospholipidsand Fish Oil Enriched with w-3 Fatty Acids from Tuna Canning Processing Teti Estiasih, Moch. Nur, Jaya Mahar Maligan, Satrio Maulana ABSTRAK Keunggulan fosfolipid dapat ditingkatkan dengan menggabungkan asam lemak w-3, terutama EPA (eicosapentaenoicacid, C20:5w-3 dan DHA (docosahexaenoic acid, C22:6w-3, pada struktur fosfolipid sehingga diperoleh fosfolipidterstruktur. Strukturisasi fosfolipid kedelai komersial dilakukan dengan cara mengganti asam lemak dari fosfolipidkedelai dengan asam lemak w-3 dari minyak kaya asam lemak w-3 dari hasil samping pengalengan tuna. Sintesisfosfolipid terstruktur dilakukan secara asidolisis enzimatis dengan menggunakan lipase dari R. miehei. Faktor yangdikaji pada proses sintesis ini adalah konsentrasi enzim dan lama sintesis. Tingkat inkorporasi EPA dan DHA padastruktur fosfolipid dipengaruhi oleh konsentrasi enzim. Pada konsentrasi enzim yang rendah, peningkatan lama reaksisetelah tingkat inkoporasi optimum tercapai cenderung menyebabkan penurunan tingkat inkorporasi EPA+DHA. Padakonsentrasi enzim yang tinggi, lama reaksi tampaknya tidak mempengaruhi tingkat inkorporasi. Tingkat inkorporasiDHA lebih tinggi dari EPA sehingga fosfolipid terstruktur yang dihasilkan sangat sesuai digunakan untuk produk panganyang memerlukan kadar DHA tinggi. Ada preferensi inkorporasi EPA+DHA pada fosfatidiletanolamin dibandingkanjenis fosfolipid yang lain.Kata kunci: Fosfolipid terstruktur, asam lemak w-3, EPA, DHA, asidolisis enzimatis ABSTRACT The superiority of soy phospholipids could be obtained by incorporation of w-3 fatty acids into phospholipids structure,especially EPA (eicosapentaenoic acid, C20:5w-3 and DHA docosahexaenoic acid, C22:6w-3. Structurization ofcommercial soy phospholipids was conducted by replacement of natural fatty acids in soy phospholipids by w-3 fattyacids from w-3 fatty acids enriched Þ sh oil from tuna canning processing

Review Of Applied Mathematical Models For Describing The Behaviour Of Aqueous Humor In Eye Structures

Science.gov (United States)

Dzierka, M.; Jurczak, P.

2015-12-01

In the paper, currently used methods for modeling the flow of the aqueous humor through eye structures are presented. Then a computational model based on rheological models of Newtonian and non-Newtonian fluids is proposed. The proposed model may be used for modeling the flow of the aqueous humor through the trabecular meshwork. The trabecular meshwork is modeled as an array of rectilinear parallel capillary tubes. The flow of Newtonian and non-Newtonian fluids is considered. As a results of discussion mathematical equations of permeability of porous media and velocity of fluid flow through porous media have been received.

Theoretical, physical and experimental study of fissile aqueous media; Etudes theorique, physique et experimentale des milieux fissiles aqueux

Energy Technology Data Exchange (ETDEWEB)

Caizergues, R. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1969-04-01

This thesis consists of a set of theoretical and experimental studies. a) Theoretical calculation methods used for cross-sections and the critical parameters; b) Comparison of the theoretical and experimental results: it is shown that the agreement between these results cannot be improved above a certain limit because of the accuracy with which are known the composition and the dimensions of the media and the microscopic cross-sections; c) Determination of the ratios {eta}{sup 9}-bar / {eta}{sup 5}-bar, {eta}{sup 3}-bar / {eta}{sup 5}-bar for fissile aqueous media ({eta}-bar: number of neutrons emitted per neutron absorbed, averaged over the reactor neutron spectrum). Evaluation of the accuracy to which these ratios are known; d) Effect of {sup 240}Pu: the measurements are carried out on Pu with a {sup 240}Pu content of 1.5 per cent, 3.11 per cent and 9.95 per cent; Calculation of the resonance integral I240 using the experimental results gives values in reasonable agreement with the results obtained by other more conventional methods. e) Measurement of the spectrum indices for aqueous media containing Pu, U5 and U3. With these latter it is possible to obtain mean fission cross-section ratios {sigma}f239-bar / {sigma}f235-bar for these different spectra. A calculation-experiment comparison is carried out using various theoretical methods. (author) [French] Cette these groupe un ensemble d'etudes theoriques et experimentales. a) Methodes theoriques de calcul utilisees pour les sections efficaces et les parametres critiques; b) Comparaisons des resultats theoriques et experimentaux: on montre que l'accord entre ces resultats ne peut etre ameliore au-dela de certaines limites vu la precision avec laquelle sont connues la composition et les dimensions des milieux et les sections efficaces macroscopiques; c) Determination des rapports {eta}{sup 9}-bar / {eta}{sup 5}-bar, {eta}{sup 3}-bar / {eta}{sup 5}-bar pour les milieux fissiles aqueux ({eta}: nombre de

Theoretical, physical and experimental study of fissile aqueous media; Etudes theorique, physique et experimentale des milieux fissiles aqueux

Energy Technology Data Exchange (ETDEWEB)

Caizergues, R [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1969-04-01

This thesis consists of a set of theoretical and experimental studies. a) Theoretical calculation methods used for cross-sections and the critical parameters; b) Comparison of the theoretical and experimental results: it is shown that the agreement between these results cannot be improved above a certain limit because of the accuracy with which are known the composition and the dimensions of the media and the microscopic cross-sections; c) Determination of the ratios {eta}{sup 9}-bar / {eta}{sup 5}-bar, {eta}{sup 3}-bar / {eta}{sup 5}-bar for fissile aqueous media ({eta}-bar: number of neutrons emitted per neutron absorbed, averaged over the reactor neutron spectrum). Evaluation of the accuracy to which these ratios are known; d) Effect of {sup 240}Pu: the measurements are carried out on Pu with a {sup 240}Pu content of 1.5 per cent, 3.11 per cent and 9.95 per cent; Calculation of the resonance integral I240 using the experimental results gives values in reasonable agreement with the results obtained by other more conventional methods. e) Measurement of the spectrum indices for aqueous media containing Pu, U5 and U3. With these latter it is possible to obtain mean fission cross-section ratios {sigma}f239-bar / {sigma}f235-bar for these different spectra. A calculation-experiment comparison is carried out using various theoretical methods. (author) [French] Cette these groupe un ensemble d'etudes theoriques et experimentales. a) Methodes theoriques de calcul utilisees pour les sections efficaces et les parametres critiques; b) Comparaisons des resultats theoriques et experimentaux: on montre que l'accord entre ces resultats ne peut etre ameliore au-dela de certaines limites vu la precision avec laquelle sont connues la composition et les dimensions des milieux et les sections efficaces macroscopiques; c) Determination des rapports {eta}{sup 9}-bar / {eta}{sup 5}-bar, {eta}{sup 3}-bar / {eta}{sup 5}-bar pour les milieux fissiles aqueux ({eta}: nombre de neutrons emis

Studies on the rates of exchange of Hg(II), Cd(II), La(III) and Ce(III) ions in sodium nitrite-aqueous acetone media using an anion-exchanger Dowex-1x8(NO3-)

International Nuclear Information System (INIS)

Bhatnagar, R.P.; Bhardwaj, Archana; Bhardwaj, S.D.

1998-01-01

Rate of exchange has been studied on Hg(II), Cd(II), La(III) and Ce(III) ions in sodium nitrite-aqueous acetone media using an anion exchanger Dowex-1 x 8(NO 3 - ). Acetone was used to provide solvent media of 10%, 30% and 50% and temperature was used in rate studies, carried out at 30 deg, 40 deg, 50 degC. Always 1 g. of Dowex-1x8 in nitrate form was used for distribution studies to get rate data. After suitable time intervals aliquots (1 ml) were withdrawn and metal ion concentration was found out. (author)

Analisis Hasil Sintesis Serbuk TiO2 / ZnO sebagai Lapisan Elektroda untuk Aplikasi Dye-sensitized Solar Cell

Directory of Open Access Journals (Sweden)

Lilis Retnaningsih

2016-06-01

Full Text Available Pada penelitian ini telah dilakukan sintesis antara serbuk partikel nano TiO2 dan serbuk partikel nano ZnO menjadi pasta yang akan diaplikasikan sebagai elektroda pada dye-sensitized solar cell (DSSC. Elektroda pada DSSC ini bekerja berdasarkan adsorbsi foton oleh pewarna, elektron yang tereksitasi ditransfer ke TiO2/ZnO yang mempunyai perbandingan berbeda. Dimensi material partikel nano TiO2/ZnO sebagai elektroda sangat penting untuk menghasilkan efisiensi yang lebih tinggi pada DSSC. Sifat ini sangat dipengaruh oleh metoda pabrikasi elektroda TiO2/ZnO dan parameternya. Pada penelitian ini digunakan metoda doctor blade untuk pabrikasi DSSC dan larutan dyes (Z907 sebagai zat pewarna. Tujuan penelitian ini adalah untuk mengetahui pengaruh pencampuran serbuk TiO2 dan serbuk ZnO sebagai elektroda. Teknik pembuatan pasta TiO2/ZnO sebagai elektroda sangat penting untuk menghasilkan efisiensi tinggi pada DSSC. Teknik ini sangat terkait dengan material TiO2/ZnO, metoda pabrikasi, dan parameter pengukurannya. Dalam penelitian ini dibahas hasil karakterisasi XRD pada kedua serbuk TiO2 dan ZnO, hasil SEM pada pencampuran kedua material, hasil pengujian IPCE serta hasil pengukuran effisiensi pada pengujian I - V.

Coupled enzyme reactions performed in heterogeneous reaction media: experiments and modeling for glucose oxidase and horseradish peroxidase in a PEG/citrate aqueous two-phase system.

Science.gov (United States)

Aumiller, William M; Davis, Bradley W; Hashemian, Negar; Maranas, Costas; Armaou, Antonios; Keating, Christine D

2014-03-06

The intracellular environment in which biological reactions occur is crowded with macromolecules and subdivided into microenvironments that differ in both physical properties and chemical composition. The work described here combines experimental and computational model systems to help understand the consequences of this heterogeneous reaction media on the outcome of coupled enzyme reactions. Our experimental model system for solution heterogeneity is a biphasic polyethylene glycol (PEG)/sodium citrate aqueous mixture that provides coexisting PEG-rich and citrate-rich phases. Reaction kinetics for the coupled enzyme reaction between glucose oxidase (GOX) and horseradish peroxidase (HRP) were measured in the PEG/citrate aqueous two-phase system (ATPS). Enzyme kinetics differed between the two phases, particularly for the HRP. Both enzymes, as well as the substrates glucose and H2O2, partitioned to the citrate-rich phase; however, the Amplex Red substrate necessary to complete the sequential reaction partitioned strongly to the PEG-rich phase. Reactions in ATPS were quantitatively described by a mathematical model that incorporated measured partitioning and kinetic parameters. The model was then extended to new reaction conditions, i.e., higher enzyme concentration. Both experimental and computational results suggest mass transfer across the interface is vital to maintain the observed rate of product formation, which may be a means of metabolic regulation in vivo. Although outcomes for a specific system will depend on the particulars of the enzyme reactions and the microenvironments, this work demonstrates how coupled enzymatic reactions in complex, heterogeneous media can be understood in terms of a mathematical model.

The study of CO2 absorption intensification using porous media material in aqueous AMP solution

Directory of Open Access Journals (Sweden)

Min Xiao

2018-03-01

Full Text Available In this work, the performance of CO2 absorption into aqueous 2-amino-2-methyl-propanol (AMP solution was investigated by measuring the amount of CO2 in the liquid phase during CO2 absorption process to identify initial CO2 absorption rate. Then, the porous media material named as MCM41 was introduced into the amine solution to test its influence on CO2 absorption. It was found that MCM41 increased initial CO2 absorption rate and enhanced CO2 absorption process. The physico-chemical properties of MCM41 were characterized in terms of specific surface area, average pore diameter, total pore volume and chemical properties, the amount of acidic sites and the Brϕnsted/Lewis (B/L acid sites ratio. Results showed that MCM41 was a type of Lewis acid catalyst with large specific surface area and pore volume. In addition, the pKa of AMP solution with and without MCM41 was obtained using acid titration technology to help understand the effect brought by MCM41. A mechanism illustrating how MCM41 increases the CO2 absorption rate of the AMP solution was proposed and demonstrated that MCM41 is a potential material for enhancing CO2 absorption.

Risks of using membrane filtration for trace metal analysis and assessing the dissolved metal fraction of aqueous media - A study on zinc, copper and nickel

International Nuclear Information System (INIS)

Hedberg, Yolanda; Herting, Gunilla; Wallinder, Inger Odnevall

2011-01-01

Membrane filtration is commonly performed for solid-liquid separation of aqueous solutions prior to trace metal analysis and when assessing 'dissolved' metal fractions. Potential artifacts induced by filtration such as contamination and/or adsorption of metals within the membrane have been investigated for different membrane materials, metals, applied pressures and pre-cleaning steps. Measurements have been conducted on aqueous solutions including well-defined metal standards, ultrapure water, and on runoff water from corroded samples. Filtration using both non-cleaned and pre-cleaned filters revealed contamination and adsorption effects, in particular pronounced for zinc, evident for copper but non-significant for nickel. The results clearly show these artifacts to be non-systematic both for non-cleaned and pre-cleaned membranes. The applied pressure was of minor importance. Measurements of the labile fraction by means of stripping voltammetry clearly elucidate that membrane filtration followed by total metal analysis cannot accurately assess the labile or the dissolved metal fraction. - Highlights: → Membrane filtration for trace metal analysis can introduce significant artifacts. → The dissolved metal fraction cannot be assessed by membrane filtration. → Non-specified filtration procedures are inadequate for scientific studies. → Artifacts caused by membrane filtration need to be addressed by regulators. - Membrane filtration cannot be used to assess the dissolved metal fraction of aqueous media and needs to be defined in detail in standard tests.

Technological development for the synthesis of Captan and Folpet in Mexico; Desarrollo tecnologico para la sintesis de Captan y Folpet en Mexico

Energy Technology Data Exchange (ETDEWEB)

Haro C, Jorge A [Universidad Autonoma Metropolitana-Iztapalapa, Mexico, D.F. (Mexico); Romero M, Artemisa; James M, Guillermo [Universidad Autonoma Metropolitana-Xochimilco, Mexico, D.F. (Mexico); Santos de Flores, Elvira [Universidad Nacional Autonoma de Mexico, Mexico, D.F. (Mexico)

1995-02-01

A technological development is presented for the production of Captan (3a, 4, 7, 7a-tetrahydro-2-[(tri-chlo-romethyl) thio]-1 H-isoindol-1, 3 (2H)-dione) and Folpet (2-(Trichloromethyl)- thio- 1 H-isoindol-1, 3-(2H)-dione), protectan fungicides for stored cereals, starting front national raw materials made in Mexico. These compounds are used for the grain protection stored in warehouse, that count the advantage of being degradables and little toxic. [Spanish] En este trabajo presentamos la adaptacion de la tecnologia a nivel laboratorio, para la sintesis de los fungicidas Captan (3a, 4, 7, 7a- te-trahidro-2-[(triclorometril) tio]-1H-iso-indol-1, 3 (2H)-diona) y Folpet (2-(tricloro-metil)-tio-1 H-isoindol-1, 3- (2H)- diona) a partir de materias primas fabricadas en Mexico. Estos compuestos son empleados para la proteccion de granos almacenados en bodega, que cuentan con la ventaja de ser degradables y poco toxicos.

phenylalanine and l-tyrosine as chiral micellar media for the cat

African Journals Online (AJOL)

polar solvents [15-18]. Hence, surfactants offer the possibility for organic reactions to occur in aqueous media, and from the viewpoint of green chemistry, water is safer, harmless and environmentally benign [19]. However, there has been limited work on the use of chiral micellar media to catalyze Diels-. Alder reactions.

Oxidation of magnetite in aerated aqueous media

International Nuclear Information System (INIS)

Taylor, P.; Owen, D.G.

1993-04-01

Metastable equilibria involving phases less stable than hematite can be significantly more oxidizing than the calculated equilibrium between well-crystallized hematite and magnetite. In this report, generalized solubility and stability relationships between magnetite and Fe 2 O 3 .xH 2 O phases are derived to describe the metastable equilibria. Experiments with synthetic magnetite powders in aerated aqueous solutions show that crystalline hematite is formed within days at temperatures above 100 C in pure water or solutions containing anions (e.g., Cl - , SO 4 2 - , HCO 3 - ) that do not form very strong surface complexes with iron oxides. In the presence of dissolved phosphate or silica, however, the dissolution-precipitation route to hematite is strongly inhibited, and maghemite is a persistent metastable product. Thus, phosphate or silica are expected to delay the approach to magnetite-hematite equilibrium in aerated groundwaters conditioned by magnetite. These findings are presented in the context of nuclear fuel waste disposal. (author). 63 refs., 1 tab., 11 figs

ELECTROCHEMICAL BEHAVIOUR OF METHYLENE BLUE IN NON-AQUEOUS SOLVENTS

International Nuclear Information System (INIS)

Caram, J.A.; Suárez, J.F. Martínez; Gennaro, A.M.; Mirífico, M.V.

2015-01-01

Graphical abstract: Display Omitted - Highlights: • The dye is electro-reduced in two separated monoelectronic charge transfers. • Solvent/supporting electrolyte/acid/base modifies the electrochemical parameters. • A dissociation equilibrium of the dye in non-aqueous solvent is proposed. • The electro-generated and stable dye-radical is also chemically produced in EDA or KOH/DMF. • A new species is reversibly formed in KOH/EtOH or ACN. - Abstract: The electrochemical behaviour of methylene blue in solution of non-aqueous solvents with different supporting electrolytes was studied by cyclic voltammetry. Dye electro-reduction presents two well-defined processes of monoelectronic charge transfer yielding a free radical in the first process and an anion in the second electron transfer. Free radical and anion are long living species in some of the studied media. Effects of supporting electrolyte and solvent on the peak potentials, the peak current functions and the reversibility of the charge transfer processes are reported. A dissociation equilibrium of the dye in solution of non-aqueous solvents and the acid or base added determine markedly the electrochemical responses. In the particular cases of KOH/DMF or EDA basic media the chemical formation of the stable methylene blue radical was detected and it was characterized by EPR spectroscopy. A general reaction scheme is proposed

Sorption of per- and polyfluoroalkyl substances (PFASs) on filter media: implications for phase partitioning studies.

Science.gov (United States)

Chandramouli, Bharat; Benskin, Jonathan P; Hamilton, M Coreen; Cosgrove, John R

2015-01-01

Per- and polyfluoroalkyl substances (PFASs), including perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS), are ubiquitous in the environment. Investigations into their fate and potential phase-partitioning behavior require separating solid from aqueous phases via filtration. However, sorption of aqueous-phase PFASs on filtration media may lead to underestimation of PFAS concentrations in the aqueous phase. The authors investigated the sorption of perfluoroalkyl carboxylates, perfluoroalkyl sulfonates, perfluoroalkyl phosphonic acids, perfluoroalkyl phosphinic acids (PFPiAs), polyfluoroalkyl phosphate monoesters, polyfluoroalkyl phosphate diesters (diPAPs), fluorotelomer sulfonates, and perfluorooctane sulfonamide on filtration media. The effects of concentration (3 spiking levels), filter media (4 types), matrix (4 matrices), and compound structure on sorption are reported. Glass fiber filtration resulted in the least sorption, whereas polytetrafluoroethylene filters resulted in the most sorption (up to 98%). Analyte concentration had no significant effect. Sorption was generally consistent across matrix types except for samples affected by aqueous film forming foam deployment, which displayed high sorption of PFOS on nylon filters. Sorption usually increased with an increasing number of carbon or fluorine atoms and was most pronounced for PFPiAs and diPAPs (30–75% sorption). Overall, glass fiber filters are more recommended than nylon filters in environmental samples when phase separation is required. Use of filtration media for PFAS must be preceded by matrix-specific testing to account for unpredictable effects. (C)2014 SETAC

Bioremediation techniques applied to aqueous media contaminated with mercury.

Science.gov (United States)

Velásquez-Riaño, Möritz; Benavides-Otaya, Holman D

2016-12-01

In recent years, the environmental and human health impacts of mercury contamination have driven the search for alternative, eco-efficient techniques different from the traditional physicochemical methods for treating this metal. One of these alternative processes is bioremediation. A comprehensive analysis of the different variables that can affect this process is presented. It focuses on determining the effectiveness of different techniques of bioremediation, with a specific consideration of three variables: the removal percentage, time needed for bioremediation and initial concentration of mercury to be treated in an aqueous medium.

Potentiodynamic polarization studies of bulk amorphous alloy Zr57Cu15.4Ni12.6Al10Nb5 and Zr59Cu20Ni8Al10Ti3 in aqueous HNO3 media

International Nuclear Information System (INIS)

Sharma, Poonam; Dhawan, Anil; Jayraj, J.; Kamachi Mudali, U.

2013-01-01

The potentiodynamic polarization studies were carried out on Zr based bulk amorphous alloy Zr 57 Cu 15.4 Ni 12.6 Al 10 Nb 5 and Zr 59 Cu 20 Ni 8 Al 10 Ti 3 in solutions of 1 M, 6 M and 11.5 M HNO 3 aqueous media at room temperature. As received specimens of Zr 57 Cu 15.4 Ni 12.6 Al 10 Nb 5 (5 mm diameter rod) and Zr 59 Cu 20 Ni 8 Al 10 Ti 3 (3 mm diameter rod) were polished with SiC paper before testing them for potentiodynamic polarization studies. The amorphous nature of the specimens was checked by X-ray diffraction. The bulk amorphous alloy Zr 59 Cu 20 Ni 8 Al 10 Ti 3 shows the better corrosion resistance than Zr 57 Cu 15.4 Ni 12.6 Al 10 Nb 5 alloy in the aqueous HNO 3 media as the value of the corrosion current density (I corr ) for Zr 57 Cu 15.4 Ni 12.6 Al 10 Nb 5 alloy were found to be more than Zr 59 Cu 20 Ni 8 Al 10 Ti 3 alloy in aqueous HNO 3 media. The improved corrosion resistance of Zr 59 Cu 20 Ni 8 Al 10 Ti 3 alloy is possibly due to the presence of Ti and formation of TiO 2 during anodic oxidation. Both Zr based bulk amorphous alloys shows wider passive range at lower concentration of nitric acid and the passive region gets narrowed down with the increase in concentration. A comparison of data obtained from both the Zr-based bulk amorphous alloys is made and results are discussed in the paper. (author)

Physicochemical characterization of in situ drug-polymer nanocomplex formed between zwitterionic drug and ionomeric material in aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Salamanca, Constain H., E-mail: chsalamanca@icesi.edu.co [Pharmaceutical physical chemistry laboratory, Department of Pharmacy, Faculty of Natural Sciences, ICESI University, Cali (Colombia); Castillo, Duvan F.; Villada, Juan D. [Pharmaceutical physical chemistry laboratory, Department of Pharmacy, Faculty of Natural Sciences, ICESI University, Cali (Colombia); Rivera, Gustavo R. [SIT Biotech GmbH, BMZ 2 Otto-Hahn-Str. 15, 44227 Dortmund (Germany)

2017-03-01

Biocompatible polymeric materials with the potential to form functional structures, in association with different therapeutic molecules, in physiological media, represent a great potential for biological and pharmaceutical applications. Therefore, here the formation of a nano-complex between a synthetic cationic polymer and model drug (ampicillin trihydrate) was studied. The formed complex was characterized by size and zeta potential measurements, using dynamic light scattering and capillary electrophoresis. Moreover, the chemical and thermodynamically stability of these complexes were studied. The ionomeric material, here referred as EuCl, was obtained by equimolar reaction between Eudragit E and HCl. The structural characterization was carried out by potentiometric titration, FTIR spectroscopy, and DSC. The effect of pH, time, polymer concentration and ampicillin/polymer molar ratio over the hydrodynamic diameter and zeta potential were established. The results show that EuCl ionomer in aqueous media presents two different populations of nanoparticles; one of this tends to form flocculated aggregates in high pH and concentrations, by acquiring different conformations in solution by changing from a compact to an extended conformation. Moreover, the formation of an in situ interfacial polymer-drug complex was demonstrated, this could slightly reduce the hydrolytic degradation of the drug while affecting its solubility, mainly under acidic conditions. - Highlights: • The EuCl ionomer in aqueous media presents two different populations of nanoparticle, corresponding to proximally 15 nm and 150 nm. • The EuCl ionomer in aqueous media may form different structure depending on the pH and polymer concentration, which tends to form flocculated aggregates in high pH and concentrations. • The formation of an in situ interfacial polymer-drug complex was demonstrated, which could slightly reduce the hydrolytic degradation of the drug and affecting its solubility in

Plutonium scrap waste processing based on aqueous nitrate and chloride media

International Nuclear Information System (INIS)

Navratil, J.D.

1985-01-01

A brief review of plutonium scrap aqueous waste processing technology at Rocky Flats is given. Nitric acid unit operations include dissolution and leaching, anion exchange purification and precipitation. Chloride waste processing consists of cation exchange and carbonate precipitation. Ferrite and carrier precipitation waste treatment processes are also described. 3 figs

Aqueous CO2 vs. aqueous extraction of soils as a preparative procedure for acute toxicity testing

International Nuclear Information System (INIS)

Yates, G.W.; Burks, S.L.

1994-01-01

This study was to determine if contaminated soils extracted with supercritical CO 2 (SFE) would yield different results from soils extracted with an aqueous media. Soil samples from an abandoned oil refinery were subjected to aqueous and SFE extraction. Uncontaminated control sites were compared with contaminated sites. Each extract was analyzed for 48 hour acute Ceriodaphnia LC50s and Microtox reg-sign EC50s. Comparisons were then made between the aqueous extracts and the SFE extracts. An additional study was made with HPLC chromatographs of the SFE contaminated site extracts to determine if there was a correlation between LC50 results and peak area of different sections of the chromatograph. The 48 hour Ceriodaphnia LC50 of one contaminated site showed a significant increase in toxicity with the supercritical extract compared to the aqueous extract. All contaminated sites gave toxic responses with the supercritical procedure. The Microtox reg-sign assay showed a toxic response with 2 of the 3 contaminated sites for both aqueous and SFE extracts. Results indicate that the Ceriodaphnia assays were more sensitive than Microtox reg-sign to contaminants found in the refinery soil. SFE controls did not show adverse effects with the Ceriodaphnia, but did have a slight effect with Microtox reg-sign. The best correlation (r 2 > 0.90) between the Ceriodaphnia LC50s and the peak areas of the chromatographs was obtained for sections with an estimated log K ow of 1 to 5. SFE extraction provided a fast, efficient and inexpensive method of collecting and testing moderately non-polar to strongly non-polar organic contaminants from contaminated soils

Modelling extraction and separation of some alpha-transition elements from acidic media by synergic combinations of aromatic polyimines and micellar cationic exchangers

International Nuclear Information System (INIS)

Vitart, X.; Musikas, C.

1988-01-01

In this paper is emphasized, taking the extraction and separation by Dinonylnaphtalene sulfonic acid (HDMNS)of ruthenium-rhodium from a nitric acid media and nickel-cobalt from a sulfuric acid media as examples, the quantified chemical equilibria involved in order to elucidate the extraction mechanism. Reactions in aqueous media were investigated within three aspects: kinetics of formation, stability of metal complexes, ionic associations between complexes and mineral anions present in acidic media. This last point explains partly the selectivity of the system. The behaviour of HDNNS within extraction conditions, was studied leading to the structure of the micelle and to the quantification of equilibria involved (critical micelle concentration, polymerisation constant, etc...). Ligand extraction was studied previously to metal complexes extraction since the general mechanism of the system proceeds as a competitive extraction of cationic species in aqueous media (protonated forms of the free ligand, cationic metal complexes). The modelling of independent extraction of metals was used to predict numerically the behaviour of a multicomponent system where few metals are initially in aqueous media. These simulations are in accordance with experimental results

Substituent effects on an inverse electron demand hetero Diels-Alder reaction in aqueous solution and organic solvents : Cycloaddition of substituted styrenes to di(2-pyridyl)-1,2,4,5-tetrazine

NARCIS (Netherlands)

Wijnen, Jan W.; Zavarise, Silvia; Engberts, Jan B.F.N.; Charton, Marvin

1996-01-01

The kinetics of the Diels-Alder reactions of di(2-pyridyl)-1,2,4,5-tetrazine (1) with substituted styrenes 2 was investigated in aqueous media and in organic solvents. The second-order rate constants ofthis reaction increase dramatically in water-rich media. A decrease in pH accelerates the aqueous

Hydrolysis of Methylal Catalyzed by Ion Exchange Resins in Aqueous Media

Science.gov (United States)

He, Gaoyin; Dai, Fangfang; Shi, Midong; Li, Qingsong; Yu, Yingmin

2018-05-01

In the present work, the chemical equilibrium and kinetics of methylal (PODE1) hydrolysis catalyzed by ion-exchange resin in aqueous solutions were investigated. The study covers temperatures between 333.15 and 363.15 K at various starting compositions covering (PODE1 + MeOH)/water molar ratio ranges from 0.5 to 1.5 in a time scale. On the basis of the experimental results, a mole fraction-based model of the chemical equilibrium and a pseudohomogeneous model are proposed to fit data based on true amount of monomeric formaldehyde. It has been demonstrated that the hydrolysis of PODE1 is slightly endothermic with the enthalpy 8.19 kJ/mol and the rate determining step. Finally, a feed-forward artificial neural networks (ANN) model is developed to model the concentration change of methanol in aqueous solutions. The results showed that the predicted data from designed ANN model were in good agreement with the experimental data with the coefficient ( R 2) of 0.98. Designed ANN provides a reliable method for modeling the hydrolysis reaction of methylal (PODE1).

Mutual diffusion of sodium hyaluranate in aqueous solutions

International Nuclear Information System (INIS)

Veríssimo, Luís M.P.; Valada, Teresa I.C.; Sobral, Abilio J.F.N.; Azevedo, Eduarda E.F.G.; Azevedo, Maria L.G.; Ribeiro, Ana C.F.

2014-01-01

Highlights: • Binary diffusion coefficients for the systems containing sodium hyaluronate. • Influence of the aggregation on diffusion of the sodium hyaluronate in the aqueous media. • Estimation of the thermodynamic and mobility factors from mutual diffusion. -- Abstract: The Taylor dispersion technique has been used for measuring mutual diffusion coefficients of sodium hyaluronate in aqueous solutions at T = 298.15 K, and concentrations ranging from (0.00 to 0.50) g · dm −3 . The results are interpreted on the basis of Nernst, and Onsager and Fuoss theoretical equations. From the diffusion coefficient at infinitesimal concentration, the limiting ionic conductivity and the tracer diffusion coefficient of hyaluronate ion were estimated. These studies have been complemented by molecular mechanics calculations

Crucible-Free Synthesis of Silicides and Borides; Synthese de siliciures et de borures sans creuset; Bestigel'nyj sintez silitsidov i boridov; Sintesis de siliciuros y boruros sin crisol

Energy Technology Data Exchange (ETDEWEB)

Ban, Z.; Sikirica, M. [Rudjer Boskovic Institute, Zagreb, Yugoslavia (Croatia)

1963-11-15

The laboratory method for preparing pure silicides and borides, reducing the corresponding oxides of metals, has been developed. Synthesis of silicides was carried out in the floating zone of molten silicon. The floating zone was obtained by means of electron bombardment. Synthesis of borides is similar but reactions are generally of the solid-solid type. Initial heating of the reaction mixture was also obtained by means of the electron beam but further heating was produced by the ionized gaseous products of the reaction. (author) [French] On a mis au point une methode pour la preparation en laboratoire de siliciures et de borures purs, par reduction des oxydes des metaux correspondants. La synthese des siliciures a pu etre faite dans la ''zone flottante'' du silicium fondu. Cette zone flottante a ete obtenue par bombardement electronique. La synthese des borures est analogue, mais les reactions ont lieu generalement a Tetat solide. Le chauffage initial du melange reactionnel a egalement ete obtenu pai bombardement electronique, mais le chauffage ulterieur etait assure par les electrons diffuses des produits ionises gazeux de la reaction. (author) [Spanish] Los autores idearon un metodo de laboratorio para preparar siliciuros y boruros puros por reduccion de los respectivos oxidos metalicos. La sintesis de los siliciuros se llevo a cabo en la zona flotante del silicio fundido. Esa zona se obtuvo por bombardeo electronico. La sintesis de los boruros se llevo a cabo de manera similar, pero generalmente las reacciones son del tipo solido-solido. El calentamiento inicial de la mezcla se efectuo tambien mediante un haz electronico, pero el calentamiento ulterior es producido por la dispersion electronica en los productos de reaccion ionizados en estado gaseoso. (author) [Russian] Razrabotan laboratornyj metod prigotovleniya chistykh silitsidov i boridov putem vosstanovleniya sootvetstvennykh okislov metalla. Sintez, silitsidov provodili v plavayushchej zone

Removal of beta-blockers from aqueous media by adsorption onto graphene oxide

Energy Technology Data Exchange (ETDEWEB)

Kyzas, George Z. [Laboratory of Polymer Chemistry and Technology, Department of Chemistry, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki (Greece); Koltsakidou, Anastasia [Laboratory of Environmental Pollution Control, Department of Chemistry, Aristotle University of Thessaloniki, GR–541 24 Thessaloniki (Greece); Nanaki, Stavroula G.; Bikiaris, Dimitrios N. [Laboratory of Polymer Chemistry and Technology, Department of Chemistry, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki (Greece); Lambropoulou, Dimitra A., E-mail: dlambro@chem.auth.gr [Laboratory of Environmental Pollution Control, Department of Chemistry, Aristotle University of Thessaloniki, GR–541 24 Thessaloniki (Greece)

2015-12-15

The aim of the present study is the evaluation of graphene oxide (GhO) as adsorbent material for the removal of beta-blockers (pharmaceutical compounds) in aqueous solutions. The composition and morphology of prepared materials were characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR). Atenolol (ATL) and propranolol (PRO) were used as model drug molecules and their behavior were investigated in terms of GhO dosage, contact time, temperature and pH. Adsorption mechanisms were proposed and the pH-effect curves after adsorption were discussed. The kinetic behavior of GhO-drugs system was analyzed after fitting to pseudo-first and -second order equations. The adsorption equilibrium data were fitted to Langmuir, Freundlich and Langmuir–Freundlich model calculating the maximum adsorption capacity (67 and 116 mg/g for PRO and ATL (25 °C), respectively). The temperature effect on adsorption was tested carrying out the equilibrium adsorption experiments at three different temperatures (25, 45, 65 °C). Then, the thermodynamic parameters of enthalpy, free energy and entropy were calculated. Finally, the desorption of drugs from GhO was evaluated by using both aqueous eluants (pH 2–10) and organic solvents. - Highlights: • Removal of beta-blockers by graphene oxide (GhO) from aqueous samples • Detailed adsorbent characterization and adsorption studies • Kinetic studies are performed and adsorption isotherms are determined and modeled. • GhO was proved to be an effective adsorbent for removal of atenolol and propranolol.

Surface grafting of cellulose nanocrystals with poly(ethylene oxide) in aqueous media.

Science.gov (United States)

Kloser, Elisabeth; Gray, Derek G

2010-08-17

Aqueous suspensions of poly(ethylene oxide)-grafted nanocrystalline cellulose (PEO-grafted NCC) were prepared in order to achieve steric instead of electrostatic stabilization. A two-step process was employed: in the first step NCC suspensions prepared by sulfuric acid hydrolysis were desulfated with sodium hydroxide, and in the second step the surfaces of the crystals were functionalized with epoxy-terminated poly(ethylene oxide) (PEO epoxide) under alkaline conditions. The PEO-grafted samples were analyzed by conductometric titration, ATR-IR, solid-state NMR, MALDI-TOF MS, SEC MALLS, and AFM. The covalent nature of the linkage was confirmed by weight increase and MALDI-TOF analysis. The PEO-grafted cellulose nanocrystals (CNCs) formed a stable colloidal suspension that remained well dispersed, while the desulfated nanoparticles aggregated and precipitated. Upon concentration of the PEO-grafted aqueous NCC suspension, a chiral nematic phase was observed.

Efficient Microwave Assisted Syntheses of 2,5-Diketopiperazines in Aqueous Media

Directory of Open Access Journals (Sweden)

María Yolanda Rios

2009-07-01

Full Text Available Aqueous in situ one-pot N-Boc-deprotection-cyclization of Nα-Boc-dipeptidyl-tert-butyl and methyl esters under microwave irradiation afforded 2,5-diketopiperazines (DKPs in excellent yields. This protocol is rapid, safe, environmentally friendly, and highly efficient, and showed that the tert-butoxy moiety is also an excellent leaving group for these cyclizations.

Physical Removal of Anions from Aqueous Media by Means of a Macrocycle-Containing Polymeric Network

KAUST Repository

Ji, Xiaofan

2018-02-13

Reported here is a hydrogel-forming polymer network that contains a water-soluble tetracationic macrocycle. Upon immersion of this polymer network in aqueous solutions containing various inorganic and organic salts, changes in the physical properties are observed that are consistent with absorption of the constituent anions into the polymer network. This absorption is ascribed to host-guest interactions involving the tetracationic macrocyclic receptor. Removal of the anions may then be achieved by lifting the resulting hydrogels out of the aqueous phase. Treating the anion-containing hydrogels with dilute HCl leads to the protonation-induced release of the bound anions. This allows the hydrogels to be recycled for reuse. The present polymer network thus provides a potentially attractive approach to removing undesired anions from aqueous environments.

Uranium chemistry in blood and aqueous media. Techniques of studies

International Nuclear Information System (INIS)

Scapolan, St.

1996-11-01

The object of this report in a first step, is to understand the chemistry of uranium in aqueous phase by specifying the behavior of this element in function of several parameters such PH, concentration of present species, temperature, ionic force. In a second step, investigation techniques are reviewed: X rays diffraction, potentiometric titrations, polarography, spectrophotometry, NMR of 13 C, 31 P, 17 O, capillary electrophoresis, laser detection. The third part brings elements to understand the uranium complexation in blood medium

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

Science.gov (United States)

McNeill, V Faye

2015-02-03

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.

Calcium isotope fractionation in liquid chromatography with benzo-18-crown-6 resin in aqueous hydrobromic acid medium

International Nuclear Information System (INIS)

Sato, Takuya; Oi, Takao

2015-01-01

Liquid chromatography operated in a breakthrough mode was employed to study calcium isotope fractionation in the aqueous hydrobromic acid medium. Highly porous silica beads, the inner pores of which were embedded with a benzo-18-crown-6 ether resin, were used as column packing material. Enrichment of heavier isotopes of calcium was observed in the frontal part of respective calcium chromatograms. The values of the isotope fractionation coefficient were on the order of 10 -3 . The observed isotope fractionation coefficient was dependent on the concentration of hydrobromic acid in the calcium feed solution; a higher HBr concentration resulted in a smaller fractionation coefficient value. The present calcium isotope effects were most probably mass-dependent, indicating that they mostly came from isotope effects based on molecular vibration. Molecular orbital calculations supported the present experimental results in a qualitative fashion. Chromatography operated in aqueous HBr media is a better system of Ca isotope separation than that operated in aqueous HCl media. (author)

Biorelevant dissolution media

DEFF Research Database (Denmark)

Ilardia-Arana, David; Kristensen, Henning G; Müllertz, Anette

2006-01-01

Biorelevant dissolution media containing bile salt and lecithin at concentrations appropriate for fed and fasted state are useful when testing oral solid formulations of poorly water-soluble drugs. Dilution of amphiphile solutions affects the aggregation state of the amphiphiles because bile salt...... is partitioned between the aqueous phase and the aggregates. The aim of the investigation was to study the effect of dilution on the size distribution of aggregates and its effect on the solubilization capacity. Clear buffered solutions of four intestinal amphiphiles (sodium glycocholate, lecithin, monoolein...

Dose monitoring in large-scale flowing aqueous media

International Nuclear Information System (INIS)

Kuruca, C.N.

1995-01-01

The Miami Electron Beam Research Facility (EBRF) has been in operation for six years. The EBRF houses a 1.5 MV, 75 KW DC scanned electron beam. Experiments have been conducted to evaluate the effectiveness of high-energy electron irradiation in the removal of toxic organic chemicals from contaminated water and the disinfection of various wastewater streams. The large-scale plant operates at approximately 450 L/min (120 gal/min). The radiation dose absorbed by the flowing aqueous streams is estimated by measuring the difference in water temperature before and after it passes in front of the beam. Temperature measurements are made using resistance temperature devices (RTDs) and recorded by computer along with other operating parameters. Estimated dose is obtained from the measured temperature differences using the specific heat of water. This presentation will discuss experience with this measurement system, its application to different water presentation devices, sources of error, and the advantages and disadvantages of its use in large-scale process applications

Studies on the behavior of plutonium(IV) in alkaline carbonate/bicarbonate media

International Nuclear Information System (INIS)

Charyulu, M.M.; Satao, K.J.; Sivaramakrishnan, C.K.; Patil, S.K.

1986-01-01

Distribution ratios of plutonium(IV) between carbonate/bicarbonate media and strong base anion exchanger Amberlyst A-26 have been measured. Distribution ratio values are much higher in case of bicarbonate medium. The equilibrium was also achieved in a very short period in this medium. These data indicate feasibility of recovery of plutonium from such aqueous media using simple ion exchange method. (author)

Development of the Aqueous Processes for Removing NOx from Flue Gases.

Science.gov (United States)

Chappell, Gilford A.

A screening study was conducted to evaluate the capability of aqueous solutions to scrub NOx from the flue gases emitted by stationary power plants fired with fossil fuels. The report summarizes the findings of this laboratory program. The experimental program studied the following media for absorption of NOx from flue gases containing no NOx:…

Magnetically Separable Fe3O4@DOPA-Pd: A Heterogeneous Catalyst for Aqueous Heck Reaction

Science.gov (United States)

Magnetically separable Fe3O4@DOPA-Pd catalyst has been synthesized via anchoring of palladium over dopamine-coated magnetite via non-covalent interaction and the catalyst is utilized for expeditious Heck coupling in aqueous media.

A reaction-based fluorescent sensor for detection of cyanide in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Wang, Shan-Teng; Sie, Yi-Wun [Department of Chemistry, National Changhua University of Education, Changhua 50058, Taiwan (China); Wan, Chin-Feng [School of Applied Chemistry, Chung Shan Medical University, Taichung City 40201, Taiwan (China); Wu, An-Tai, E-mail: antai@cc.ncue.edu.tw [Department of Chemistry, National Changhua University of Education, Changhua 50058, Taiwan (China)

2016-05-15

A simple boronic acid derivative was utilized as a reaction-based receptor for CN{sup −} in aqueous solution. The receptor showed a selective and sensitive response to CN{sup −} over other various anions via nucleophilic addition of CN{sup −} to the imine moiety of the boronic-based receptor.

Removal of Hg, As in FGD gypsum by different aqueous ammonia (amines) during CO2 sequestration.

Science.gov (United States)

Wenyi, Tan; Wenhui, Fan; Hongyi, Li; Zixin, Zhang; Yunkun, Zhu

2017-12-01

CO 2 sequestration by flue gas desulfurization gypsum (FGDG) has become a promising FGDG disposal technology due to simultaneous CO 2 emission reduction and FGDG conversion into calcium carbonate. In this paper, another merit of the novel technology, i.e., the removal of toxic elements (e.g., Hg and As) in FGDG, will be addressed for the first time. In three different aqueous ammonia (or amines) media, removal efficiencies of Hg and As in FGDG samples were evaluated during CO 2 sequestration. Higher than 90% and 20% removal efficiencies, respectively, for Hg and As are achieved at 40°C in aqueous ammonia media, but they decrease at elevated temperatures. Ammonia loss takes place at 80°C and pH varies greatly with temperatures in aqueous ammonia. This is disadvantageous for the formation of Hg-ammonia complexes and for the yield of carbonates, which are responsible for Hg or As re-adsorption. The sequential chemical extraction method suggests that the speciation changes of Hg are induced by FGDG carbonation, and that unstable Hg speciation in triethanolamine increases at elevated temperatures.

Control of Electrostatic Interactions Between F-Actin And Genetically Modified Lysozyme in Aqueous Media

International Nuclear Information System (INIS)

Sanders, L.K.; Xian, W.; Guaqueta, C.; Strohman, M.; Vrasich, C.R.; Luijten, E.; Wong, G.C.L.

2009-01-01

The aim for deterministic control of the interactions between macroions in aqueous media has motivated widespread experimental and theoretical work. Although it has been well established that like-charged macromolecules can aggregate under the influence of oppositely charged condensing agents, the specific conditions for the stability of such aggregates can only be determined empirically. We examine these conditions, which involve an interplay of electrostatic and osmotic effects, by using a well defined model system composed of F-actin, an anionic rod-like polyelectrolyte, and lysozyme, a cationic globular protein with a charge that can be genetically modified. The structure and stability of actin-lysozyme complexes for different lysozyme charge mutants and salt concentrations are examined by using synchrotron x-ray scattering and molecular dynamics simulations. We provide evidence that supports a structural transition from columnar arrangements of F-actin held together by arrays of lysozyme at the threefold interstitial sites of the actin sublattice to marginally stable complexes in which lysozyme resides at twofold bridging sites between actin. The reduced stability arises from strongly reduced partitioning of salt between the complex and the surrounding solution. Changes in the stability of actin-lysozyme complexes are of biomedical interest because their formation has been reported to contribute to the persistence of airway infections in cystic fibrosis by sequestering antimicrobials such as lysozyme. We present x-ray microscopy results that argue for the existence of actin-lysozyme complexes in cystic fibrosis sputum and demonstrate that, for a wide range of salt conditions, charge-reduced lysozyme is not sequestered in ordered complexes while retaining its bacterial killing activity.

Ultrasound promoted one-pot synthesis of 2-amino-4,8-dihydropyrano[3,2-b]pyran-3-carbonitrile scaffolds in aqueous media: a complementary 'green chemistry' tool to organic synthesis.

Science.gov (United States)

Banitaba, Sayed Hossein; Safari, Javad; Khalili, Shiva Dehghan

2013-01-01

A green and simple approach to assembling of 2-amino-4,8-dihydropyrano[3,2-b]pyran-3-carbonitrile scaffolds via three-component reaction of kojic acid, malononitrile, and aromatic aldehydes in aqueous media under ultrasound irradiation is described. The combinatorial synthesis was achieved for this methodology with applying ultrasound irradiation while making use of water as green solvent. In comparison to conventional methods, experimental simplicity, good functional group tolerance, excellent yields, short routine, and selectivity without the need for a transition metal or base catalyst are prominent features of this green procedure. Copyright © 2012 Elsevier B.V. All rights reserved.

Imaging biofilm in porous media using X-ray computed microtomography.

Science.gov (United States)

Davit, Y; Iltis, G; Debenest, G; Veran-Tissoires, S; Wildenschild, D; Gerino, M; Quintard, M

2011-04-01

In this study, a new technique for three-dimensional imaging of biofilm within porous media using X-ray computed microtomography is presented. Due to the similarity in X-ray absorption coefficients for the porous media (plastic), biofilm and aqueous phase, an X-ray contrast agent is required to image biofilm within the experimental matrix using X-ray computed tomography. The presented technique utilizes a medical suspension of barium sulphate to differentiate between the aqueous phase and the biofilm. Potassium iodide is added to the suspension to aid in delineation between the biofilm and the experimental porous medium. The iodide readily diffuses into the biofilm while the barium sulphate suspension remains in the aqueous phase. This allows for effective differentiation of the three phases within the experimental systems utilized in this study. The behaviour of the two contrast agents, in particular of the barium sulphate, is addressed by comparing two-dimensional images of biofilm within a pore network obtained by (1) optical visualization and (2) X-ray absorption radiography. We show that the contrast mixture provides contrast between the biofilm, the aqueous-phase and the solid-phase (beads). The imaging method is then applied to two three-dimensional packed-bead columns within which biofilm was grown. Examples of reconstructed images are provided to illustrate the effectiveness of the method. Limitations and applications of the technique are discussed. A key benefit, associated with the presented method, is that it captures a substantial amount of information regarding the topology of the pore-scale transport processes. For example, the quantification of changes in porous media effective parameters, such as dispersion or permeability, induced by biofilm growth, is possible using specific upscaling techniques and numerical analysis. We emphasize that the results presented here serve as a first test of this novel approach; issues with accurate segmentation of

Oxidation of hydrogen peroxide by [Ni (cyclam)] in aqueous acidic ...

Indian Academy of Sciences (India)

Oxidation of hydrogen peroxide by tris(2,2 -bipyridine) and tris(4,4 -dimethyl-2,2 - bipyridine) complexes of osmium(III), iron(III), ruthenium(III), and nickel(III) studied in acidic and neutral aqueous media, show an inverse acid depen- dence over the pH the range 6.0–8.5.12 Kinetic mea- surements with an excess of H2O2 ...

Colloid transport in dual-permeability media

Science.gov (United States)

Leij, Feike J.; Bradford, Scott A.

2013-07-01

It has been widely reported that colloids can travel faster and over longer distances in natural structured porous media than in uniform structureless media used in laboratory studies. The presence of preferential pathways for colloids in the subsurface environment is of concern because of the increased risks for disease caused by microorganisms and colloid-associated contaminants. This study presents a model for colloid transport in dual-permeability media that includes reversible and irreversible retention of colloids and first-order exchange between the aqueous phases of the two regions. The model may also be used to describe transport of other reactive solutes in dual-permeability media. Analytical solutions for colloid concentrations in aqueous and solid phases were obtained using Laplace transformation and matrix decomposition. The solutions proved convenient to assess the effect of model parameters on the colloid distribution. The analytical model was used to describe effluent concentrations for a bromide tracer and 3.2- or 1-μm-colloids that were observed after transport through a composite 10-cm long porous medium made up of a cylindrical lens or core of sand and a surrounding matrix with sand of a different grain size. The tracer data were described very well and realistic estimates were obtained for the pore-water velocity in the two flow domains. An accurate description was also achieved for most colloid breakthrough curves. Dispersivity and retention parameters were typically greater for the larger 3.2-μm-colloids while both reversible and irreversible retention rates tended to be higher for the finer sands than the coarser sand. The relatively small sample size and the complex flow pattern in the composite medium made it difficult to reach definitive conclusions regarding transport parameters for colloid transport.

Effect of liquid active media on grinding and scratching of solids

International Nuclear Information System (INIS)

Pertsov, N.V.; Danilova, F.B.; Babat, I.G.

1975-01-01

In the present paper the influence of various liquid active media on grinding of tungsten carbide, hard alloy T 15 K 6, oxide of aluminium A995 and other materials with diamond grinding wheels is investigated. A grinding device is described. The results of the investigations show that materials with metallic type of bonds are most effectively treated in the medium of liquid metals; for material with an ionic structure the active media are water and aqueous solutions of electrolytes. It is pointed out that liquid active media will diminish the specific work of dispergation by as much as one order of magnitude

Effect of aqueous media on the copper-ion-mediated phototoxicity of CuO nanoparticles toward green fluorescent protein-expressing Escherichia coli.

Science.gov (United States)

Shang, Enxiang; Li, Yang; Niu, Junfeng; Guo, Huiyuan; Zhou, Yijing; Liu, Han; Zhang, Xinqi

2015-12-01

Quantitative comparison of different aqueous media on the phototoxicity of copper oxide nanoparticles (CuO NPs) is crucial for understanding their ecological effects. In this study, the phototoxicity of CuO NPs toward the green fluorescent protein-expressing Escherichia coli (GFP-E. coli) under UV irradiation (365 nm) was investigated in Luria-Bertani medium (LB), NaCl solution, deionized water (DI) and phosphate-buffered saline (PBS). The phototoxicity of CuO NPs toward GFP-E. coli decreased in the order of DI>NaCl>PBS>LB because of different released concentrations of Cu(2+). The 3h released Cu(2+) concentrations by 10mg/L CuO NPs in DI water, NaCl solution, LB medium, and PBS were 1946.3 ± 75.6, 1242.5 ± 47.6, 1023.4 ± 41.2, and 1162.1 ± 41.9 μg/L, respectively. Transmission electron microscope and laser scanning confocal microscope images of E. coli exposed to CuO NPs demonstrated that the released Cu(2+) resulted in fragmentation of bacterial cell walls, leakage of intracellular components, and finally death of bacteria in four media after UV light irradiation. In each medium, the bacterial mortality rate logarithmically increased with the releasing concentrations of Cu(2+) by CuO NPs (R(2)>0.90) exposed to 3h UV light. This study highlights the importance of taking into consideration of water chemistry when the phototoxicity of CuO NPs is assessed in nanotoxicity research. Copyright © 2015 Elsevier Inc. All rights reserved.

Synergistic extraction of transition metal cations from aqueous media by two separated organic phases

International Nuclear Information System (INIS)

Goldberg, I.

1991-12-01

We have therefore initiated novel approaches to the study of the mechanism of the synergistic extraction of metal ions by means of two separated organic phases, which are brought in contact with the same aqueous phase. The present work is concerned with the extraction of transition metals and actinides ions from nitric acid by chelating agents e.g., HTTA thenoyltrifluoroacetone in a diluent - the first organic phase, and by natural donor, e.g., TBP, tri-butyl phosphate in a diluent the second organic phase. The adduct formation was studied by means of spectrochemical and radiochemical methods. In the first approach the aqueous phase was attacked with both organic phases simultanously (the static or parallel extraction). In this method organic phase are separated one from the other. It was shown that even in the absence of mixing, synergism is observed under this experimental conditions. The results indicate, that adduct formation occurs in both organic phases. Nevertheless the enhanchment of extraction in the TBP phase is by far greater than that in the HTTA containing phase. This approach has one disadvatage, viz., the experiments are very time consuming, a typical experiment requiring over 10 days. In order to overcome this difficulty, the following experiments were carried out: the aqueous phase were first shaken with diluent containing an anionic ligand and the phases were allowed to separate. Then the aqueous solution were shaken with diluent containing a netural donor and the phase again were allowed to separate. The concentration of the metal ions in all the phases were determined. The experiments were repeated with an other diluent replacing the first diluent in one or both organic phases. In this way eight sequences of experiments were carried out for each concentration set chosen. The results thus point out that this experimental approach open new possibilities to investigate the mechanism and the kinetics of synergistic extraction processes. (author) the

Rheological Properties of Aqueous Nanometric Alumina Suspensions

Energy Technology Data Exchange (ETDEWEB)

Li, Chuanping [Iowa State Univ., Ames, IA (United States)

2004-01-01

Colloidal processing is an effective and reliable approach in the fabrication of the advanced ceramic products. Successful colloidal processing of fine ceramic powders requires accurate control of the rheological properties. The accurate control relies on the understanding the influences of various colloidal parameters on the rheological properties. Almost all research done on the rheology paid less attention to the interactions of particle and solvent. However, the interactions of the particles are usually built up through the media in which the particles are suspended. Therefore, interactions of the particle with the media, the adsorbed layers on the particle surface, and chemical and physical properties of media themselves must influence the rheology of the suspension, especially for the dense suspensions containing nanosized particles. Relatively little research work has been reported in this area. This thesis addresses the rheological properties of nanometric alumina aqueous suspensions, and paying more attention to the interactions between particle and solvent, which in turn influence the particle-particle interactions. Dense nanometric alumina aqueous suspensions with low viscosity were achieved by environmentally-benign fructose additives. The rheology of nanometric alumina aqueous suspensions and its variation with the particle volume fraction and concentration of fructose were explored by rheometry. The adsorptions of solute (fructose) and solvent (water) on the nanometric alumina particle surfaces were measured and analyzed by TG/DSC, TOC, and NMR techniques. The mobility of water molecules in the suspensions and its variation with particle volume fractions and fructose additive were determined by the ¹⁷O NMR relaxation method. The interactions between the nanometric alumina particles in water and fructose solutions were investigated by AFM. The results indicated that a large number of water layers were physically bound on the particles

Polarographic studies about indium (III) behaviour in aqueous media of sodium azide

International Nuclear Information System (INIS)

Tokoro, R.

1988-01-01

The present study shows some polarographic behavior of indium (III) in azide media that is close those observed in a thiocyanate solution. The presence of azide ligand decreases the overpotential in the discharge of indium whose catalytic character can be explained by formation of an azide bridge between electrode and indium (III) increasing the speed of electron transfer. The discharge of indium in azide media is diffusion controlled. As the azide concentration is increased the half wave potential displaces in the cathodic direction. This displacement is due to complex formation. The number of electrons, n, involved in the total process was estimates by the reversible polarographic equation to be 2,7. The potentiostatic coulometry of indium in azide/hydrazoic acid buffer showed a catalytic process where the chemistry regeneration was performed by reaction of hydrazoic acid and indium amalgam. The electrochemistry evidence was the constancy of current as the electrolysis proceeded. The chemistry aspect was the presence of ammonium cation in electrolysed solution. The catalytic process with chemistry regeneration and the formation of a bridge by azide could explain the higher value of current in azide media compared to perchlorate solution. (author) [pt

HYDROBIOGEOCHEM: A coupled model of HYDROlogic transport and mixed BIOGEOCHEMical kinetic/equilibrium reactions in saturated-unsaturated media

Energy Technology Data Exchange (ETDEWEB)

Yeh, G.T.; Salvage, K.M. [Pennsylvania State Univ., University Park, PA (United States). Dept. of Civil and Environmental Engineering; Gwo, J.P. [Oak Ridge National Lab., TN (United States); Zachara, J.M.; Szecsody, J.E. [Pacific Northwest National Lab., Richland, WA (United States)

1998-07-01

The computer program HYDROBIOGEOCHEM is a coupled model of HYDROlogic transport and BIOGEOCHEMical kinetic and/or equilibrium reactions in saturated/unsaturated media. HYDROBIOGEOCHEM iteratively solves the two-dimensional transport equations and the ordinary differential and algebraic equations of mixed biogeochemical reactions. The transport equations are solved for all aqueous chemical components and kinetically controlled aqueous species. HYDROBIOGEOCHEM is designed for generic application to reactive transport problems affected by both microbiological and geochemical reactions in subsurface media. Input to the program includes the geometry of the system, the spatial distribution of finite elements and nodes, the properties of the media, the potential chemical and microbial reactions, and the initial and boundary conditions. Output includes the spatial distribution of chemical and microbial concentrations as a function of time and space, and the chemical speciation at user-specified nodes.

A critical overview of non-aqueous capillary electrophoresis. Part II: separation efficiency and analysis time.

Science.gov (United States)

Kenndler, Ernst

2014-03-28

A survey of the literature on non-aqueous capillary zone electrophoresis leaves one with the impression of a prevailing notion that non-aqueous conditions are principally more favorable than conventional aqueous media. Specifically, the application of organic solvents in capillary zone electrophoresis (CZE) is believed to provide the general advantages of superior separation efficiency, higher applicable electric field strength, and shorter analysis time. These advantages, however, are often claimed without providing any experimental evidence, or based on rather uncritical comparisons of limited sets of arbitrarily selected separation results. Therefore, the performance characteristics of non-aqueous vs. aqueous CZE certainly deserve closer scrutiny. The primary intention of Part II of this review is to give a critical survey of the literature on non-aqueous capillary electrophoresis (NACE) that has emerged over the last five years. Emphasis is mainly placed on those studies that are concerned with the aspects of plate height, plate number, and the crucial mechanisms contributing to zone broadening, both in organic and aqueous conditions. To facilitate a deeper understanding, this treatment covers also the theoretical fundamentals of peak dispersion phenomena arising from wall adsorption; concentration overload (electromigration dispersion); longitudinal diffusion; and thermal gradients. Theoretically achievable plate numbers are discussed, both under limiting (at zero ionic strength) and application-relevant conditions (at finite ionic strength). In addition, the impact of the superimposed electroosmotic flow contributions to overall CZE performance is addressed, both for aqueous and non-aqueous media. It was concluded that for peak dispersion due to wall adsorption and due to concentration overload (electromigration dispersion, leading to peak triangulation) no general conjunction with the solvent can be deduced. This is in contrast to longitudinal diffusion: the

Non-Boussinesq Dissolution-Driven Convection in Porous Media

Science.gov (United States)

Amooie, M. A.; Soltanian, M. R.; Moortgat, J.

2017-12-01

Geological carbon dioxide (CO2) sequestration in deep saline aquifers has been increasingly recognized as a feasible technology to stabilize the atmospheric carbon concentrations and subsequently mitigate the global warming. Solubility trapping is one of the most effective storage mechanisms, which is associated initially with diffusion-driven slow dissolution of gaseous CO2 into the aqueous phase, followed by density-driven convective mixing of CO2 throughout the aquifer. The convection includes both diffusion and fast advective transport of the dissolved CO2. We study the fluid dynamics of CO2 convection in the underlying single aqueous-phase region. Two modeling approaches are employed to define the system: (i) a constant-concentration condition for CO2 in aqueous phase at the top boundary, and (ii) a sufficiently low, constant injection-rate for CO2 from top boundary. The latter allows for thermodynamically consistent evolution of the CO2 composition and the aqueous phase density against the rate at which the dissolved CO2 convects. Here we accurately model the full nonlinear phase behavior of brine-CO2 mixture in a confined domain altered by dissolution and compressibility, while relaxing the common Boussinesq approximation. We discover new flow regimes and present quantitative scaling relations for global characters of spreading, mixing, and dissolution flux in two- and three-dimensional media for the both model types. We then revisit the universal Sherwood-Rayleigh scaling that is under debate for porous media convective flows. Our findings confirm the sublinear scaling for the constant-concentration case, while reconciling the classical linear scaling for the constant-injection model problem. The results provide a detailed perspective into how the available modeling strategies affect the prediction ability for the total amount of CO2 dissolved in the long term within saline aquifers of different permeabilities.

La catalyse enzymatique en milieu organique Enzymatic Catalysis in Organic Media

Directory of Open Access Journals (Sweden)

Monot F.

2006-11-01

Full Text Available L'environnement naturel des enzymes étant de nature aqueuse, leurs applications industrielles se sont en général limitées à des réactions mettant en jeu des substrats solubles dans l'eau. Depuis quelques années, la possibilité de faire fonctionner des enzymes dans des milieux hydrophobes (hydrocarbures, solvants organiques a été mise en évidence, engendrant ainsi de nombreux travaux visant, d'une part à mieux comprendre les mécanismes permettant aux enzymes de rester actives dans un tel environnement et, d'autre part à explorer les nouvelles applications envisageables. Les produits pétroliers constituant par excellence le domaine des molécules hydrophobes, le présent article se propose de faire le point sur ces deux aspects, compréhension et intérêt de la catalyse enzymatique en milieu organique. Nous détaillerons ainsi les vues actuelles sur le fonctionnement des enzymes dans des solvants organiques, les différents modes de mise en oeuvre possibles et, à travers une revue de leurs applications potentielles, les principaux systèmes enzymatiques utilisés. The extension of enzymatic catalysis, classically carried out in aqueous media, to organic media can be first ascribed to the possibility of using substrates that are poorly soluble or insoluble in water. In biphasic media consisting of an aqueous phase containing the enzyme in solution and of a non water-miscible organic solvent, the enzyme is kept in a suitable aqueous environment. A variant biphasic system consists in creating reverse micelles by the addition of a surfactant in order to increase the interfacial area and thus to improve the transfers between the aqueous phase where the enzyme is located and the organic phase. In these two cases, the partition coefficient of the different reactants plays a crucial role by governing the rates and yields of reaction. Microaqueous media constitute a new system for biocatalysis in organic media. In this case, a solid enzyme

Radiation protection of vitamins in aqueous systems

International Nuclear Information System (INIS)

Kishore, K.; Moorthy, P.N.; Rao, K.N.

1976-01-01

A study of the radiation induced decomposition of the B-group vitamins has been carried out in aqueous media at room temperature as well as in rigid matrices at low temperature. The detailed results on the effect of glucose and oxygen as protective additives at the different temperatures are presented in the case of Thiamine (Vitamin B 1 ). Comparative data are given on the extent of decomposition of this and other vitamins of the B-group at room temperature and at 193 K. The importance of these results in connection with the radiation sterilization of pharmaceutical preparations is indicated. (author)

Preparation of SBA-15-PAMAM as a Nano Adsorbent for Removal of Acid Red 266 from Aqueous Media: Batch Adsorption and Equilibrium Studies

Directory of Open Access Journals (Sweden)

Maryam Mirzaie

2017-12-01

Full Text Available The purpose of the present study was to increase the adsorption capacity of SBA-15 for acidic dyes. Ordered mesoporous silica SBA-15 was successfully synthesized and functionalized by polyamidoamine (PAMAM dendrimer to develop an efficient anionic dye adsorbent. The prepared materials were characterized by field emission scanning electron microscope (FE-SEM, Fourier transforms infrared spectroscope (FT-IR and N2 adsorption–desorption analysis. The study was concocted in the Science and Research Branch of Islamic Azad University of Tehran, Iran in 2016. The produced adsorbent (SBA-15-Den was applied for the removal of Acid Red 266 (AR266 from aqueous media. The effects of various operational parameters including solution pH, adsorbent dosage, contact time, and temperature on removal of AR266 using SBA-15-Den were investigated in batch adsorption mode. Within the optimum conditions, SBA-15-Den exhibited an excellent adsorptive capability of 1111.11 mg/g. Equilibrium data were best described by Langmuir model (R2 > 0.98 completely.

Tandem Aldol-Michael Reactions in Aqueous Diethylamine Medium: A Greener and Efficient Approach to Bis-Pyrimidine Derivatives

Directory of Open Access Journals (Sweden)

Abdullah M. Al-Majid

2013-12-01

Full Text Available A simple protocol, involving the green synthesis for the construction of novel bis-pyrimidine derivatives, 3a–i and 4a–e are accomplished by the aqueous diethylamine media promoted tandem Aldol-Michael reaction between two molecules of barbituric acid derivatives 1a,b with various aldehydes. This efficient synthetic protocol using an economic and environmentally friendly reaction media with versatility and shorter reaction time provides bis-pyrimidine derivatives with high yields (88%–99%.

Dithizone as novel and efficient chromogenic probe for cyanide detection in aqueous media through nucleophilic addition into diazenylthione moiety.

Science.gov (United States)

Tavallali, Hossein; Deilamy-Rad, Gohar; Parhami, Abolfath; Kiyani, Sajede

2014-01-01

A new selective chemodosimeter probe was developed by the introduction of dithizone (DTZ) as a simple and available dye for detection of cyanide in aqueous media which enables recognition of cyanide over other competing anions such as acetate, dihydrogen phosphate, fluoride and benzoate through covalent bonding. The sensing properties of DTZ were investigated in DMSO/H2O (1:9) and have demonstrated a very high selectivity toward the cyanide anions. A reasonable recognition mechanism was suggested using UV-Vis, (1)H NMR and FTIR spectroscopy techniques. Time dependent density function theory (TDDFT) computations of UV-Vis excitation for DTZ2-CN adduct agreed well with our experimental findings. The detection limit of the new chromogenic probe was measured to be 0.48 μmol L(-1) which is much lower than most recently reported chromogenic probes for cyanide determination. The analytical utility of the method for the analysis of cyanide ions in electroplating wastewater (EPWW), human serum, tap and mineral water samples was demonstrated and the results were compared successfully with the conventional reference method. The short time response and the detection by the naked eye make the method available for the detection and quantitative determination of cyanide in a variety of real samples. Copyright © 2013 Elsevier B.V. All rights reserved.

Enumeration of sugars and sugar alcohols hydroxyl groups by aqueous-based acetylation and MALDI-TOF mass spectrometry

Science.gov (United States)

A method is described for enumerating hydroxyl groups on analytes in aqueous media is described, and applied to some common polyalcohols (erythritol, mannitol, and xylitol) and selected carbohydrates. The analytes were derivatized in water with vinyl acetate in presence of sodium phosphate buffer. ...

On the validity of a Fickian diffusion model for the spreading of liquid infiltration plumes in partially saturated heterogeneous media

International Nuclear Information System (INIS)

Pruess, K.

1994-01-01

Localized infiltration of aqueous and -non-aqueous phase liquids (NAPLs) occurs in many circumstances. Examples include leaky underground pipelines and storage tanks, landfill and disposal sites, and surface spills. Because of ever-present heterogeneities on different scales such infiltration plumes are expected to disperse transversally and longitudinally. This paper examines recent suggestions that liquid plumes are being dispersed from medium heterogeneities in a manner that is analogous to Fickian diffusion. Numerical simulation experiments on liquid infiltration in heterogeneous media are performed to study the dispersive effects of small-scale heterogeneity. It is found that plume spreading indeed tends to be diffusive. Our results suggest that, as far as infiltration of liquids is concerned, broad classes of heterogeneous media behave as dispersive media with locally homogeneous (albeit anisotropic) permeability

Heterogeneous self-assembled media for biopolymerization

DEFF Research Database (Denmark)

Monnard, Pierre-Alain

2011-01-01

Heterogeneous media, such as micro-structured aqueous environments, could offer an alternative approach to the synthesis of biopolymers with novel functions. Structured media are here defined as specialized, self-assembled structures that are formed, e.g, by amphiphiles, such as liposomes, emulsion...... polymerization, the initial elongation rates clearly depended on the complementarity of the monomers with the templating nucleobases3. However, metal-ion catalyzed reactions deliver RNA analogs with heterogeneous linkages. Moreover, the usefulness of this medium in the form of quasi-compartmentalization extends...... beyond metal-ion catalysis reactions, as we have recently demonstrated the catalytic power of a dipeptide, SerHis, for the regioselective formation of phosphodiester bonds. These results in conjonction with the synthesis of nucleobases at -78˚C, the demonstration of ribozyme activity (RNA ligase ribozyme...

Sonochemical synthesis of a PdAg/C electrocatalyst for oxygen reduction reaction; Sintesis sonoquimica de un electrocatalizador de PdAg/C para la reaccion de reduccion de oxigeno

Energy Technology Data Exchange (ETDEWEB)

Godinez-Garcia, A.; Perez-Robles, J.F. [Centro de Investigacion y de Estudios Avanzados del IPN. Santiago de Queretaro, Queretaro (Mexico)]. E-mail: jperez@qro.cinvestav.mx; Solorza-Feria, O. [CINVESTAV-IPN, Mexico, D.F. (Mexico)

2009-09-15

The synthesis and characterization of nanocatalysts for fuel cells has been a primary line of research for the purpose of obtaining less expensive electrocatalysts with better activity. A large variety of methods exist to synthesize useful nanoparticles as electrocatalysts. Each method generates particles with a different surface morphology and, therefore, the catalytic activity usually varies depending on which is used in the synthesis. In this work, PdAg/C electrocatalysts are synthesized with high-intensity ultrasonic irradiation and compared to those obtained using a conventional method such as reduction by NaBH{sub 4}. The study of this technique is of interest because it produces highly dispersed carbon-supported nanoparticles with very clean surfaces. Each electrocatalyst was evaluated for its oxygen reduction reaction (ORR) in acid medium with cyclic voltamperometry (CV) and rotating disc electrode (RDE). The electrocatalyst was characterized with x-ray diffraction and transmission electron microscopy (TEM). The physical characterization reveals that the electrocatalyst is composed of nanometric bimetallic aggregates. An important characteristic of the PdAg/C alloy obtained using ultrasound is better activity than that obtained by reduction with NaBH{sub 4}. [Spanish] La sintesis y caracterizacion de nanocatalizadores para celdas de combustible ha sido una de las principales lineas de investigacion, con el objetivo de obtener electrocatalizadores mas baratos y con una mejor actividad. Existen una gran variedad de metodos para sintetizar nanoparticulas utiles como electrocatalizadores, cada metodo genera particulas con una morfologia superficial diferente por lo que la actividad catalitica suele variar dependiendo de cual se utilice en la sintesis. En este trabajo se sintetizan electrocatalizadores de PdAg/C con irradiacion ultrasonica de alta intensidad y se comparan con las obtenidas con un metodo convencional como es la reduccion por NaBH{sub 4}. Esta

Nonequilibrium gas absorption in rotating permeable media

Science.gov (United States)

Baev, V. K.; Bazhaikin, A. N.

2016-08-01

The absorption of ammonia, sulfur dioxide, and carbon dioxide by water and aqueous solutions in rotating permeable media, a cellular porous disk, and a set of spaced-apart thin disks has been considered. The efficiency of cleaning air to remove these impurities is determined, and their anomalously high solubility (higher than equilibrium value) has been discovered. The results demonstrate the feasibility of designing cheap efficient rotor-type absorbers to clean gases of harmful impurities.

Silica coating of luminescent quantum dots prepared in aqueous media for cellular labeling

Energy Technology Data Exchange (ETDEWEB)

Ma, Yunfei; Li, Yan, E-mail: yli@ecust.edu.cn; Zhong, Xinhua, E-mail: zhongxh@ecust.edu.cn

2014-12-15

Graphical abstract: A facile route based on modified Stöber method was used for the synthesis of silica coated QDs (QD@SiO{sub 2}) starting from aqueously prepared CdTe/CdS QDs. The resultant QD@SiO{sub 2} exhibited a significant increase in emission efficiency compared with that of the initial QDs, along with a small size (∼5 nm in diameter), great stability and low cytotoxicity, which makes it a good candidate as robust biomarker. - Highlights: • We present a facile modified Stöber method to prepare highly luminescent QD@SiO{sub 2}. • The PL efficiency of QDs increases significantly after silica coating. • QD@SiO{sub 2} exhibits small size (∼5 nm) and great dispersibility in aqueous solution. • QD@SiO{sub 2} presents extraordinary photo and colloidal stability. • The silica shell eliminates QD cytotoxicity, providing the access of bioconjugation. - Abstract: Silica coating is an effective approach for rendering luminescent quantum dots (QDs) with water dispersibility and biocompatibility. However, it is still challenging to prepare silica-coated QDs (QD@SiO{sub 2}) with high emission efficiency, small size and great stability in favor for bioapplication. Herein, we reported a modified Stöber method for silica coating of aqueously-prepared CdTe/CdS QDs. With the coexistence of Cd{sup 2+} and thioglycolic acid (TGA), a thin silica shell was formed around QDs by the hydrolysis of tetraethyl orthosilicate (TEOS). The resultant QD@SiO{sub 2} with a small size (∼5 nm in diameter) exhibits significantly higher emission efficiencies than that of the initial QDs. Also, QD@SiO{sub 2} has extraordinary photo and colloidal stability (pH range of 5–13, 4.0 M NaCl solution). Protected by the silica shell, the cytotoxicity of QDs could be reduced. Moreover, the QD@SiO{sub 2} conjugated with folic acid (FA) presents high specific binding toward receptor-positive HeLa cells over receptor-negative A549 cells.

Physical Removal of Anions from Aqueous Media by Means of a Macrocycle-Containing Polymeric Network

KAUST Repository

Ji, Xiaofan; Wu, Ren-Tsung; Long, Lingliang; Guo, Chenxing; Khashab, Niveen M.; Huang, Feihe; Sessler, Jonathan L.

2018-01-01

Reported here is a hydrogel-forming polymer network that contains a water-soluble tetracationic macrocycle. Upon immersion of this polymer network in aqueous solutions containing various inorganic and organic salts, changes in the physical

Method for the preparation of new X-ray contrast media

International Nuclear Information System (INIS)

1977-01-01

The chemical preparation is described of contrast media possessing an optimal combination of the following parameters: non-toxicity, non-ionogenicity, osmolality, viscosity, stability, ease and cheapness of preparation. Triiodinated and substituted isophtalamides are used with hydroxyethyl or hydroxypropyl groups as substituents. The result is an aqueous solution of isomers, from which the meso-isomer was removed by crystallization

Separation of Nanoparticles in Aqueous Multiphase Systems through Centrifugation

KAUST Repository

Akbulut, Ozge; Mace, Charles R.; Martinez, Ramses V.; Kumar, Ashok A.; Nie, Zhihong; Patton, Matthew R.; Whitesides, George M.

2012-01-01

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

Separation of Nanoparticles in Aqueous Multiphase Systems through Centrifugation

KAUST Repository

Akbulut, Ozge

2012-08-08

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

Removal of arsenic from potable water by adsorptive media treatment techniques

International Nuclear Information System (INIS)

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

2012-01-01

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

Effect of temperature and salting-out agents on the sorption of nitrophenols from aqueous solutions

Directory of Open Access Journals (Sweden)

E. V. Churilina

2013-01-01

Full Text Available Sorption of nitrophenols from aqueous media by сrosslinked N-vinylpyrrolidone-based polymer in static conditions are studied depending on the pH of the solution and the nature of the nitrophenols. It has been established that a temperature and the introduction of salting-out agents influence on the sorption of nitrophenols.

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

Science.gov (United States)

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

2010-01-01

Aqueous biphasic systems (ABS) provide an alternative and efficient approach for the extraction, recovery and purification of biomolecules through their partitioning between two liquid aqueous phases. In this work, the ability of hydrophilic phosphonium-based ionic liquids (ILs) to form ABS with aqueous K3PO4 solutions was evaluated for the first time. Ternary phase diagrams, and respective tie-lines and tie-lines length, formed by distinct phosphonium-based ILs, water, and K3PO4 at 298 K, were measured and are reported. The studied phosphonium-based ILs have shown to be more effective in promoting ABS compared to the imidazolium-based counterparts with similar anions. Moreover, the extractive capability of such systems was assessed for distinct biomolecules (including amino acids, food colourants and alkaloids). Densities and viscosities of both aqueous phases, at the mass fraction compositions used for the biomolecules extraction, were also determined. The evaluated IL-based ABS have been shown to be prospective extraction media, particularly for hydrophobic biomolecules, with several advantages over conventional polymer-inorganic salt ABS. PMID:20480041

Characterisation of the aqueous corrosion process in NdFeB melt spun ribbon and MQI bonded magnets

Science.gov (United States)

McCain, Stephen

A major factor limiting the use and longevity of rare earth based magnetic materials is their susceptibility to aqueous corrosion and associated detrimental effects upon the magnetic properties of the material. This process was investigated through a combination of exposure to simulated environmental conditions and hydrogen absorption/desorption studies (HADS) in conjunction with magnetic characterisation. This study utilises NdFeB MQP-B melt-spun ribbon manufactured by Magnequench, in the form of MQI bonded magnets and also in its unbonded state as MQ powder. Specifically, it was concerned with how effective a variety of bonding media (epoxy resin,PTFE, zinc) and surface coatings (PTFE, Qsil, zinc LPPS, Dex-Cool) were at limiting the impact of aqueous corrosion in MQI bonded magnets. To characterise the effect of hydrogen absorption upon the magnetic properties of the MQP-B, hydrogen uptake was induced followed by a series of outgassing heat treatments with subsequent magnetic characterisation accompanied by HADS techniques performed after each outgas. This allowed comparisons to be made between the effects of aqueous corrosion process and hydrogen absorption upon the magnetic properties of the alloy.. This study has clearly demonstrated the link between the abundance of environmental moisture and rate of Hci losses in MQI bonded magnets. In addition to this the key mechanism responsible for the degradation of magnetic properties has been identified. These losses have been attributed to the absorption of hydrogen generated by the dissociation of water in the presence of NdFeB during the aqueous corrosion process. It has been shown that the use of a bonding media that is impermeable to water can limit the effects of aqueous corrosion by limiting water access to the Magnequench particles (MQP) and also the positive effects of the use of suitable surface coatings has been shown to be effective for the same reason..

One-pot fabrication of FRET-based fluorescent probe for detecting copper ion and sulfide anion in 100% aqueous media

Science.gov (United States)

Lv, Kun; Chen, Jian; Wang, Hong; Zhang, Peisheng; Yu, Maolin; Long, Yunfei; Yi, Pinggui

2017-04-01

The design of effective tools for detecting copper ion (Cu2 +) and sulfide anion (S2 -) is of great importance due to the abnormal level of Cu2 + and S2 - has been associated with an increase in risk of many diseases. Herein, we report on the fabrication of fluorescence resonance energy transfer (FRET) based fluorescent probe PF (PEI-FITC) for detecting Cu2 + and S2 - in 100% aqueous media via a facile one-pot method by covalent linking fluorescein isothiocyanate (FITC) with branched-polyethylenimine (b-PEI). PF could selectively coordinate with Cu2 + among 10 metal ions to form PF-Cu2 + complex, resulting in fluorescence quenching through FRET mechanism. Furthermore, the in situ generated PF-Cu2 + complex can be used to selectively detect S2 - based on the displacement approach, resulting in an off-on type sensing. There is no obvious interference from other anions, such as Cl-, NO3-, ClO4-, SO42 -, HCO3-, CO32 -, Br-, HPO42 -, F- and S2O32 -. In addition, PF was successfully used to determine Cu2 + and S2 - in human serum and tap water samples. Therefore, the FRET-based probe PF may provide a new method for selective detection of multifarious analysts in biological and environmental applications, and even hold promise for application in more complicated systems.

Measurement of Solute Diffusion Behavior in Fractured Waste Glass Media

International Nuclear Information System (INIS)

Saripalli, Kanaka P.; Lindberg, Michael J.; Meyer, Philip D.

2008-01-01

Determination of aqueous phase diffusion coefficients of solutes through fractured media is essential for understanding and modeling contaminants transport at many hazardous waste disposal sites. No methods for earlier measurements are available for the characterization of diffusion in fractured glass blocks. We report here the use of time-lag diffusion experimental method to assess the diffusion behavior of three different solutes (Cs, Sr and Pentafluoro Benzoic Acid or PFBA) in fractured, immobilized low activity waste (ILAW) glass forms. A fractured media time-lag diffusion experimental apparatus that allows the measurement of diffusion coefficients has been designed and built for this purpose. Use of time-lag diffusion method, a considerably easier experimental method than the other available methods, was not previously demonstrated for measuring diffusion in any fractured media. Hydraulic conductivity, porosity and diffusion coefficients of a solute were experimentally measured in fractured glass blocks using this method for the first time. Results agree with the range of properties reported for similar rock media earlier, indicating that the time-lag experimental method can effectively characterize the diffusion coefficients of fractured ILAW glass media

Solubility behavior of narcotic analgesics in aqueous media: solubilities and dissociation constants of morphine, fentanyl, and sufentanil.

Science.gov (United States)

Roy, S D; Flynn, G L

1989-02-01

The pH dependence of the aqueous solubility of morphine, fentanyl, and sufentanil was investigated at 35 degrees C. Dissociation constants and corresponding pKa' values of the drugs were obtained from measured free-base solubilities (determined at high pH's) and the concentrations of saturated solutions at intermediate pH's. Morphine, fentanyl, and sufentanil exhibited pKa' values of 8.08, 8.99, and 8.51, respectively. Over the pH range of 5 to 12.5 the apparent solubilities are determined by the intrinsic solubility of the free base plus the concentration of ionized drug necessary to satisfy the dissociation equilibrium at a given pH. Consequently, the drug concentrations of saturated aqueous solutions fall off precipitously as the pH is raised and ionization is suppressed. Further, at low pH's the aqueous solubility of morphine increased in a linear fashion with increases in the molar strength of citric acid which was added to acidify the medium, suggesting the formation of a soluble morphine-citrate complex.

Monolayer and multilayer adsorption isotherm models for sorption from aqueous media

Energy Technology Data Exchange (ETDEWEB)

Saadi, Reyhaneh; Saadi, Zahra; Fazaeli, Reza; Fard, Narges Elmi [Islamic Azad University, Tehran (Iran, Islamic Republic of)

2015-05-15

Industrial wastewater polluted with various contaminants, including heavy metals, dyes, etc., endangers human health and the environment. Various separation techniques have been developed for the removal of pollutants from aqueous solutions. Adsorption process has drawn considerable attention due to its simplicity of design, high removal efficiency, even at dilute concentration, and economical aspect. We reviewed the most common two, three, four, and five parameter adsorption isotherm models corresponding to monolayer and multilayer adsorption on the basis of parameters that can be used for exploring novel adsorbents. Thermodynamic assumptions of the models give information about the surface properties, capacity of the adsorbent and adsorption mechanism. Seven error functions were investigated to evaluate the fitness quality of isotherm models with the experimental equilibrium data.

Aqueous synthesis of high bright Ag{sub 2}Se−ZnSe quantum dots with tunable near-infrared emission

Energy Technology Data Exchange (ETDEWEB)

Che, Dongchen; Ding, Di [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201602 (China); Wang, Hongzhi, E-mail: wanghz@dhu.edu.cn [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201602 (China); Zhang, Qinghong [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201602 (China); Li, Yaogang, E-mail: yaogang_li@dhu.edu.cn [Engineering Research Center of Advanced Glass Manufacturing Technology, Ministry of Education, Donghua University, Shanghai 201602 (China)

2016-09-05

Efficient aqueous synthetic methods for near-infrared quantum dots as bioimaging agents are urgently required. In this work, a simple and fast synthesis of highly luminescent, near-infrared Ag{sub 2}Se quantum dots (QDs) in aqueous media is reported. The method avoids high temperature, pressure and organic solvents to directly generate water-dispersible Ag{sub 2}Se QDs. The photoluminescence emission of Ag{sub 2}Se QDs ranges from 835 to 940 nm by different Ag:Se molar ratio. Using the ZnSe as a shell, the quantum yield reaches up to 42%. The Ag{sub 2}Se−ZnSe QDs with high quantum yield, near-infrared and low cytotoxic could be used as good cell labels, showing great potential applications in bio-imaging. - Highlights: • Ag{sub 2}Se−ZnSe nanocrystals are prepared directly in aqueous media at low temperature. • Ag{sub 2}Se−ZnSe nanocrystals show excellent water solubility and colloidal stability. • Ag{sub 2}Se nanocrystals exhibit tunable near-infrared emission with ultrasmall size. • Ag{sub 2}Se−ZnSe nanocrystals show high quantum yield with low cytotoxicity. • Ag{sub 2}Se−ZnSe nanocrystals are stable over a month at room temperature in the air.

Determination of uranyl nitrate diffusion coefficients in organic and aqueous media using the porous diaphragm method

International Nuclear Information System (INIS)

Chierice, G.O.

1974-01-01

The diffusion coefficient is one of the parameters necessary for the obtention of the extraction exponential coefficients, that are contained within the H.T.U. (height of transfer unity) calculation expression, when operating with continuous organic phase. The organic phase used was tri-n-butyl-phosphate (TBP) and varsol in the 35% and 65% proportions respectively. After each experiment, the uranium content present in each compartment was spectrophotometrically determined and the quantities contained in the aqueous phases were determined by means of volumetric titration. It was found out that the uranyl ion diffusion coefficient is two and one half times less in organic phase, this just being attributed to the greater interactions of the uranyl ions in organic than in aqueous medium

Gemini surfactant for fluorescent and stable quantum dots in aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Li Haibing [Key Laboratory of Pesticide and Chemical Biology (CCNU), Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079 (China); Wang Xiaoqiong [Key Laboratory of Pesticide and Chemical Biology (CCNU), Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079 (China); Gao Zhinong [Department of Chemistry, Wuhan University, Wuhan 430072 (China); He Zhike [Department of Chemistry, Wuhan University, Wuhan 430072 (China)

2007-05-23

Highly fluorescent and stable CdSe/ZnS core/shell quantum dots (QDs) coated with gemini surfactant are successfully synthesized in aqueous media. Analyses of luminescence spectrometry, ultraviolet-visible (UV-vis) spectrophotometry, and transmission electron micrographs (TEMs) indicate that the water-soluble QDs are monodisperse and have a luminescence enhancement compared with the original hydrophobic QDs. The water-soluble QDs coated with gemini surfactant are shown to be biocompatible, photostable, and have been proven to be suitable for live cell imaging.

Gemini surfactant for fluorescent and stable quantum dots in aqueous solution

International Nuclear Information System (INIS)

Li Haibing; Wang Xiaoqiong; Gao Zhinong; He Zhike

2007-01-01

Highly fluorescent and stable CdSe/ZnS core/shell quantum dots (QDs) coated with gemini surfactant are successfully synthesized in aqueous media. Analyses of luminescence spectrometry, ultraviolet-visible (UV-vis) spectrophotometry, and transmission electron micrographs (TEMs) indicate that the water-soluble QDs are monodisperse and have a luminescence enhancement compared with the original hydrophobic QDs. The water-soluble QDs coated with gemini surfactant are shown to be biocompatible, photostable, and have been proven to be suitable for live cell imaging

A novel water soluble solvatochromic probe as a micropolarity reporter for homogeneous and microheterogeneous media

Energy Technology Data Exchange (ETDEWEB)

Sarkar, Amrita; Kedia, Niraja [Department of Chemical Sciences, Indian Institute of Science Education and Research, Kolkata, Mohanpur Campus, BCKV Main P.O., Mohanpur 741252, Nadia, WB (India); Bagchi, Sanjib, E-mail: bsanjibb@yahoo.com [Department of Chemistry and Biochemistry, Presidency University, 86/1 College Street, Kolkata 700073 (India)

2014-07-01

A new water soluble donor–acceptor dye, sodium 4-(methyl((1E,3E)-3-(1-oxo-1H-inden-2(3H)-ylidene)prop-1-enyl)amino) benzoate (DN3) has been synthesized. Optical response of the solvatochromic dye (DN3) has been studied in various homogeneous (neat and mixed binary solvents) and heterogeneous (SDS and CTAB homomicelle and β-cyclodextrin nanocavity) media. To get information regarding the change in the solvation interaction of the dye with the alteration in its microenvironment in different media, the photophysical properties of the dye have been monitored in various media using steady state and time resolved spectral analysis. Results obtained for mixed binary solvents containing water indicate that the solute is preferentially solvated by one of the component solvents and solvent–solvent interactions are also important in determining the preference. Effect of variation of pH in aqueous medium on the spectroscopic parameters of the dye has been studied and its pKa has been estimated. Studies in homomicelles (SDS and CTAB) reveal that the dye distributes itself between the aqueous and the micellar phase and the values of distribution coefficient have been estimated from the fluorescence parameters. The dye is encapsulated in β-cyclodextrin nanocavity and a 1:2 dye-β-cyclodextrin host–guest interaction is indicated. Semi-empirical quantum chemical calculations have been carried out to support the experimental results. - Highlights: • A water soluble fluorescent dye has been synthesized and studied in various media. • The dye is sensitive towards changes in micropolarity and pH of the medium. • Study in mixed binary solvent system indicates preferential solvation of the dye. • Stronger interaction of the dye is indicated with CTAB micelles compared to SDS. • Study in aqueous β-CD medium reveals favorable 1:2 binding of the dye with β-CD.

Determination of micelle formation of ketorolac tromethamine in aqueous media by acoustic measurements

International Nuclear Information System (INIS)

Savaroglu, Gokhan; Genc, Lütfi

2013-01-01

Graphical abstract: Value of critical micelle concentration (CMC) were detected by speed of sound and determined by an analytical method based on the Phillips definition of the CMC. Highlights: ► The aim of this study was to investigate the aggregation behaviour of KT. ► Influence of KT concentration and temperature upon volumetric properties was studied. ► CMC of KT aqueous solution was determined by using speeds of sound measurements. - Abstract: Density and speed of sound of ketorolac tromethamine in aqueous solutions have been measured as a function of concentration at atmospheric pressure and in the temperature range from 293.15 to 313.15 K. Apparent molar volumes, apparent isentropic compressibility and isentropic compressibility values have also been calculated from the experimental density and speed of sound data. Partial molar volume and partial molar isentropic compressibility are obtained from fitting procedures the data on apparent molar volume, V φ , and apparent isentropic compressibility, K φ(S) . Partial molar volume, V φ 0 , and partial molar isentropic compressibility, k φ(S) 0 , are informative thermodynamic characteristics that reflect solute hydration. The critical micelle concentration (CMC) was determined from speed of sound data by an analytical method based on the Phillips definition of the CMC. Using these results, it was possible to establish the solvent–drug interactions.

The use of some local plants for removal of radioactive and trace elements from aqueous media

International Nuclear Information System (INIS)

Al-Masri, M. S.; Amin, Y.; Al-Akel, B; Al-Naama, T.

2008-02-01

The removal of metal ions from aqueous solutions by biosorption plays an important role in water pollution control. In this study, dried leaves of Barbary, Jew's mallow and poplar, branches of poplar trees and creeping club as biomass for removal of toxic elements (Cd, Pb and U) and some radionuclides ( 133 Ba, 137 Cs and 226 Ra) from aqueous solution have been evaluated. The results show that all studied plants can be effectively used for removing U and Ba from aqueous solutions, while Pb was removed using branches of poplar trees. In addition, Cd was removed using Barbary, Jew's mallow and branches of poplar trees. The adsorption of U and Cd by leaves of Barbary reached 3.3 mg g -1 and 3.5 mg g -1 , respectively. Moreover, the leaves of poplar trees were the best plant for biosorping Pb, its maximum capacity reached a value 1.7 mg g -1 . On the other hand, the maximum capacity for studied radionuclide was less than 10-6 mg g -1 . Further more, the effect of many factors such as, plant pretreatment, solution temperature, pH, plant particles size and contact time, on biosorption process were performed and the best conditions of biosorption were recognized. The studied plants were used for removing 226 Ra and some trace elements from real polluted water. The results show that the method is effective.(author)

Dissolution and Protection of Aluminium Oxide in Corrosive Aqueous Media - An Ellipsometry and Reflectometry Study

NARCIS (Netherlands)

Karlsson, P.M.; Postmus, B.R.; Palmqvist, A.E.C.

2009-01-01

Dissolution of alumina has been studied from wafers in aqueous solution by means of ellipsometry and reflectometry. It was discovered that the dissolution of aluminium oxide is promoted by ethanol amines like N,N-bis(2-hydroxyethyl)glycine and triethanolamine, and that this dissolution is retarded

Nanoscopic surfactant behavior of the porin MspA in aqueous media

Directory of Open Access Journals (Sweden)

Ayomi S. Perera

2013-04-01

Full Text Available The mycobacterial porin MspA is one of the most stable channel proteins known to date. MspA forms vesicles at low concentrations in aqueous buffers. Evidence from dynamic light scattering, transmission electron microscopy and zeta-potential measurements by electrophoretic light scattering indicate that MspA behaves like a nanoscale surfactant. The extreme thermostability of MspA allows these investigations to be carried out at temperatures as high as 343 K, at which most other proteins would quickly denature. The principles of vesicle formation of MspA as a function of temperature and the underlying thermodynamic factors are discussed here. The results obtained provide crucial evidence in support of the hypothesis that, during vesicle formation, nanoscopic surfactant molecules, such as MspA, deviate from the principles underlined in classical surface chemistry.

The use of physiological solutions or media in calcium phosphate synthesis and processing.

Science.gov (United States)

Tas, A Cuneyt

2014-05-01

This review examined the literature to spot uses, if any, of physiological solutions/media for the in situ synthesis of calcium phosphates (CaP) under processing conditions (i.e. temperature, pH, concentration of inorganic ions present in media) mimicking those prevalent in the human hard tissue environments. There happens to be a variety of aqueous solutions or media developed for different purposes; sometimes they have been named as physiological saline, isotonic solution, cell culture solution, metastable CaP solution, supersaturated calcification solution, simulated body fluid or even dialysate solution (for dialysis patients). Most of the time such solutions were not used as the aqueous medium to perform the biomimetic synthesis of calcium phosphates, and their use was usually limited to the in vitro testing of synthetic biomaterials. This review illustrates that only a limited number of research studies used physiological solutions or media such as Earle's balanced salt solution, Bachra et al. solutions or Tris-buffered simulated body fluid solution containing 27mM HCO3(-) for synthesizing CaP, and these studies have consistently reported the formation of X-ray-amorphous CaP nanopowders instead of Ap-CaP or stoichiometric hydroxyapatite (HA, Ca10(PO4)6(OH)2) at 37°C and pH 7.4. By relying on the published articles, this review highlights the significance of the use of aqueous solutions containing 0.8-1.5 mMMg(2+), 22-27mM HCO3(-), 142-145mM Na(+), 5-5.8mM K(+), 103-133mM Cl(-), 1.8-3.75mM Ca(2+), and 0.8-1.67mM HPO4(2-), which essentially mimic the composition and the overall ionic strength of the human extracellular fluid (ECF), in forming the nanospheres of X-ray-amorphous CaP. Copyright © 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Dynamic viscosity versus probe-reported microviscosity of aqueous mixtures of poly(ethylene glycol)

International Nuclear Information System (INIS)

Bhanot, Chhavi; Trivedi, Shruti; Gupta, Arti; Pandey, Shubha; Pandey, Siddharth

2012-01-01

Highlights: ► Aqueous polymer mixtures, non-toxic media of huge industrial importance, are investigated. ► Bulk viscosity of aqueous. PEG mixtures is shown to vary widely with composition and temperature. ► T-dependent viscosity follows Arrhenius behavior suggesting aqueous PEGs to be Newtonian fluids. ► Microviscosity sensed by a fluorescence ratiometric probe is estimated and correlated with viscosity. ► Microviscosity correlates well with bulk viscosity at higher PEG concentrations. - Abstract: Correlation between the dynamic viscosity (η) and the microviscosity of a hybrid green medium constituted of water and poly(ethylene glycol) (PEG) of average molar mass (200, 400, and 600) g · mol −1 , respectively, is explored over the temperatures range (10 to 90) °C across the complete composition regime. The microviscosity is obtained using a fluorescence probe 1,3-bis-(1-pyrenyl)propane (BPP), which is manifested through the ratio of the monomer-to-intramolecular excimer intensities (I M /I E ). Aqueous PEG mixtures are observed to behave similar to Newtonian fluids as the temperature dependence of dynamic viscosity follows Arrhenius-type behavior. Surprisingly, a simple and convenient linear dependence of ln η with wt% PEG of the mixture is established. The BPP I M /I E is observed, in general, to increase with the bulk dynamic viscosity of the mixture having >10 wt% PEG suggesting a good correlation between the bulk dynamic viscosity and BPP-reported microviscosity when the viscosity of the aqueous PEG mixture is relatively high.

Effect of aqueous vitamin B on the growth of blister blight pathogen, Exobasidium vexans

Directory of Open Access Journals (Sweden)

Hideyuki Nagao

2012-12-01

Full Text Available The effect of three aqueous solution of biotin, thiamine and calcium pantothenate, on the growth of Exobasidiumvexans was examined in vitro. The germination process of basidiospores of E. vexans differed from those of the otherExobasidium species. Basidiospore germination commenced after 19.5 hr incubation and chlamydospore-like bodies wereformed after 96 hr of incubation. Addition of biotin, calcium pantothenate, and thiamine to Difco PDA and Czapek’s mediumdid not affect the proportion of germinating basidiospores. The length of germ tubes was enhanced only by addition ofthiamine in the media. Larger size germ tubes (thick germ tubes were occasionally observed among the ordinary hyphae.Most germlings of basidiospores developed chlamydospore-like bodies or autolysed on the media. Thick germ tubesfrequently appeared on the calcium pantothenate amended media and developed into a colony when these hyphae weretransferred to new calcium pantothenate amended media. However, further transfer of colonies did not successfully bring anew colony to grow on the calcium pantothenate amended media. Vitamin B5, calcium pantothenate, was only partially effective in generating the thick germ tubes and to induce the initial colony formation, whereas amendment of biotin and thiamineto the media did not induce visible colony growth.

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

Energy Technology Data Exchange (ETDEWEB)

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

1999-02-12

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

Sorption behaviour of uranium and thorium on hydrous tin oxide from aqueous and mixed-solvent HNO3 media

International Nuclear Information System (INIS)

Misak, N.Z.; Salama, H.N.; El-Naggar, I.M.

1983-01-01

In aqueous nitric acid, uranyl and thorium ions seem to be sorbed on hydrous tin oxide mainly by a cation exchange mechanism. In 10 - 3 M aqueous solutions, the hydrous oxide prefers thorium to uranium at the relative low pH values, while the reverse is true at the higher pH values. The exchange of uranium is particle diffusion controlled while that of thorium is chemically controlled, and the isotherms point to the presence of different-energy sites in the hydrous oxide. Except for the solutions containing 80% of methanol, ethanol, or acetone, cation exchange is probably still the main mechanism of sorption of uranium. Anionic sorption of thorium seems to occur in all the mixed-solvent solutions and is perhaps the main mechanism in 80% ethanol. The equilibrium distribution coefficient K sub (d) increases almost in all cases with organic solvent content, probably due to dehydration of sorbed ions and to increasing superposition on anionic sorption. Unlike the aqueous medium, large U/Th separation factors are achieved in many of the mixed-solvent solutions and separation schemes are suggested. (Authors)

Evaluation, engineering and development of advanced cyclone processes. Final separating media evaluation and test report (FSMER). Appendices

Energy Technology Data Exchange (ETDEWEB)

NONE

1996-05-01

This report consists of appendices pertaining to the separating media evaluation (calcium nitrate solution) and testing for an advanced cyclone process. Appendices include: materials safety data, aqueous medium regeneration, pH control strategy, and other notes and data.

Multi-metallic oxides as catalysts for light alcohols and hydrocarbons from synthesis gas

Energy Technology Data Exchange (ETDEWEB)

Perez, Miguel [Instituto Mexicano del Petroleo, Mexico, D.F. (Mexico); Diaz, L; Galindo, H de J; Dominguez, J. M; Salmon, Manuel [Universidad Nacional Autonoma de Mexico, Mexico, D.F. (Mexico)

1999-08-01

A series of Cu-Co-Cr oxides doped with alkaline metals (M), were prepared by the coprecipitation method with metal nitrates (Cu{sup I}I, CO{sup I}I, CR{sup I}II) and (M{sub 2})CO{sub 3} in aqueous solution. The calcined products were used as catalysts for the Fisher-Tropsch synthesis in a stainless-steel fixed bed microreactor. The material was characterized by x-ray diffraction, and the specific surface area, pore size and nitrogen adsorption-desorption properties were also determined. The alkaline metals favored the methanol synthesis and prevent the dehydration reactions whereas the hydrocarbon formation is independent to these metals. [Spanish] Una serie de oxidos Cu-Co-Cr soportados con metales alcalinos (M), fueron preparados por el metodo con nitratos metalicos (Cu{sup I}I, CO{sup I}I, CR{sup I}II) y (M{sub 2})CO{sub 3} en soluciones acuosas. Los productos calcinados fueron usados como catalizadores para la sintesis de Fisher-tropsch en la superficie fija de un microreactor de acero inoxidable. El material fue caracterizado por difraccion de rayos X y el area de superficie especifica, el tamano de poro y propiedades de absorcion-desorcion de nitrogeno fueron determinadas. Los metales alcalinos favorecieron la sintesis de metanol y previnieron las reacciones de deshidratacion, mientras que la formacion de hidrocarburos es independiente de estos metales.

Removal of mercury(II) from aqueous media using eucalyptus bark: Kinetic and equilibrium studies

International Nuclear Information System (INIS)

Ghodbane, Ilhem; Hamdaoui, Oualid

2008-01-01

In this study, eucalyptus camaldulensis bark, a forest solid waste, is proposed as a novel material for the removal of mercury(II) from aqueous phase. The operating variables studied were sorbent dosage, ionic strength, stirring speed, temperature, solution pH, contact time, and initial metal concentration. Sorption experiments indicated that the sorption capacity was dependent on operating variables and the process was strongly pH-dependent. Kinetic measurements showed that the process was uniform and rapid. In order to investigate the mechanism of sorption, kinetic data were modeled using the pseudo-first-order and pseudo-second-order kinetic equations, and intraparticle diffusion model. Among the kinetic models studied, the pseudo-second-order equation was the best applicable model to describe the sorption process. Equilibrium isotherm data were analyzed using the Langmuir and the Freundlich isotherms. The Langmuir model yields a much better fit than the Freundlich model. Isotherms have also been used to obtain the thermodynamic parameters such as free energy, enthalpy, and entropy of sorption. The maximum sorption capacity was 33.11 mg g -1 at 20 deg. C and the negative value of free energy change indicated the spontaneous nature of sorption. These results demonstrate that eucalyptus bark is very effective in the removal of Hg(II) from aqueous solutions

Nonaqueous phase liquid dissolution and soil organic matter sorption in porous media: review of system similarities

NARCIS (Netherlands)

Heyse, Edward; Augustijn, Dionysius C.M.; Suresh, P.; Rao, C.; Delfino, Joseph J.

2002-01-01

We examine similarities in constraints to mass transfer of hydrophobic organic compounds (HOCs) between the aqueous and various organic phases in porous media at the grain scale. Published research and data are reviewed regarding equilibrium coefficients and first-order rate constants for mass

A unidirectional acoustic cloak for multilayered background media with homogeneous metamaterials

Science.gov (United States)

Zhu, Jian; Chen, Tianning; Liang, Qingxuan; Wang, Xiaopeng; Xiong, Jie; Jiang, Ping

2015-08-01

The acoustic cloak, which can make an object hard to detect acoustically in a homogeneous background, has attracted great attention from researchers in recent years. The inhomogeneous background media were considered in this paper. The relative constitutive parameters were derived for acoustic cloaks working in multilayered media. And a unidirectional acoustic cloak for layered background media was proposed, designed and implemented successfully in a wide frequency range. In water and NaCl aqueous solution, the acoustic cloak was designed and realized with homogeneous metamaterials which were composed of steel and porous materials. The effective parameters of the unit cells of the cloak were determined by using the effective medium theory. Numerical results demonstrated excellent cloaking performance and showed that such a device could be physically realized with natural materials which will greatly promote the real applications of an invisibility cloak in inhomogeneous backgrounds.

On the selection of the anode material for the electrochemical removal of methylparaben from different aqueous media

International Nuclear Information System (INIS)

Steter, Juliana R.; Brillas, Enric; Sirés, Ignasi

2016-01-01

Highlights: • Comparative performance of EO-H 2 O 2 , EF and PEF with BDD, Pt and DSA as anodes. • Poor effect of anode on methylparaben mineralization by PEF but large effect in EO-H 2 O 2 . • Pseudo-first-order decay kinetics in EO-H 2 O 2 and much quicker complex kinetics in PEF. • Beneficial effect of Cl − in EO-H 2 O 2 but slightly or significantly detrimental in EF and PEF. • Quickest degradation in PEF with BDD, yielding chlorinated and non-chlorinated by-products. - Abstract: Parabens are widely used industrial preservatives, routinely found in wastewater along with major inorganic ions like sulfate and chloride. This work investigates the oxidation ability of three electrochemical processes in tank reactors equipped with an air-diffusion cathode to electrogenerate H 2 O 2 on site, namely electro-oxidation (EO-H 2 O 2 ), electro-Fenton (EF) and UVA photoelectro-Fenton (PEF), to degrade aqueous solutions of methylparaben (MeP) at pH 3.0. Their performance using boron-doped diamond (BDD), Pt or two kinds of dimensionally stable anodes (DSA ® ) has been compared from the analysis of mineralization profiles and decay kinetics in the presence of sulfate and/or chloride ions. The use of BDD ensured the overall mineralization in all three processes according to the sequence: PEF > EF > EO-H 2 O 2 , thanks to the contribution of BDD(·OH), ·OH and UVA light. Pt and DSA ® became an interesting alternative in PEF, with slower organic matter removal but similar final mineralization percentages, being much less powerful than BDD in EO-H 2 O 2 . The presence of Cl − was beneficial in the latter process, due to the formation of active chlorine as an additional oxidant that caused a much faster decay of MeP. Conversely, it became significantly detrimental in EF due to the partial destruction of H 2 O 2 and ·OH in the bulk by active chlorine and Cl − , respectively. The oxidation power of PEF was so high that similar fast, complex decay kinetics was

Novel synthetic approach for 1, 4-dihydroxyanthraquinone and the development of its Lithiated salts as anode material for aqueous rechargeable Lithium-ion batteries

KAUST Repository

Gurukar, Suresh Shivappa; Rajashekara Shetty, Vijeth; Mariappa, Ramaiah; Kittappa, Mahadevan Malavalli; Nagaraju, Doddahalli H.

2015-01-01

of active species in the aqueous media, reasonable discharge capacity with 0.9 V average voltages and agreeable cycling performance during charge-discharge process with reproducibility are achieved. For the construction of the full cell, the anode material

The Effect of Aqueous and Ethanolic Extracts of Teucrium polium on Candida Albicans and Two Species of Malassezia

Directory of Open Access Journals (Sweden)

Maryam Nadimi

2013-08-01

Full Text Available Background: Teucrium polium L. is a medicinal plant, which due to its antimicrobial, antispasmodic and anti-tumor properties has been used in traditional medicine for over 2000 years. The aim of this research was to study the effect of aqueous and ethanolic extracts of Teucrium polium L. against three strains of Candida albicans (ATCC 62061, ATCC 1677, and NCPF 3153, Malassezia furfur and Malassezia globosa using pour plate method. Materials and Methods: Teucrium polium L. was collected from Broojen area during the spring. The plant was dried and powdered. The aqueous and ethanolic extracts were prepared from the fine powder. Different concentrations of extracts (1, 2, 4, and 8 mg/ml were made in Sabouraud Dextrose Agar (SDA and modified Leeming-Notman Agar (MLNA medium for Candida albicans, Malassezia furfur and Malassezia globosa. 1.5×106 cfu/ml of yeasts, were cultured on media and incubated at 37ºC and 32ºC respectively. Pour plate method was used to assess the antifungal activity of these extracts.Results: The inhibitory effect of ethanolic extract of Teucrium polium L. on the three strains of Candida albicans was depended on concentration level of extracts in media. Aqueous extract had inhibitory effect on Candida albicans (NCPF 3153 only, and with increasing of the extract concentration, the number of colonies was decreased, so that in concentration of 8 mg/ml, no growth was seen. Aqueous and ethanolic extracts had no inhibitory effect on Malassezia species. Conclusion: Teucrium polium L. extracts have considerable inhibitory effect on different strains of Candida albicans. Further investigations are needed to detect the effectiveness of this plant in treatment of Candida infections.

Solvent extraction of Zn(II) from aqueous sulphate media by di(2-ethylhexyl) phosphoric acid in kerosene

International Nuclear Information System (INIS)

Begum, D.A.; Alauddin, M.; Rahman, M.S.

2009-01-01

The extraction equilibrium studies of Zn(II) from sulphate medium by di(2-ethylhexyl) phosphoric acid (D2EHPA, H/sub 2/A/sub 2/) in kerosene revealed that the distribution ratio (D) decreased with the increase of initial (Zn(A(II) in the aqueous phase and increased with the increase of equilibrium pH and extractant concentration. The equilibration is reached within 2 min. The species extracted into the organic phase is thought to be ZnA2, HA. The pH and extractant dependencies were about 2 and 1.67, respectively. The distribution ratio decreased with the increase in sulphate ion concentration in the aqueous phase. The extraction equilibrium reaction is suggested as Zn/sup 2+/ /sub aq/ +1.5 (H/sub 2/A/sub 2/)org - (ZnA/sub 2/, HA)org +2H/sup +/ /sub aq/. The extraction equilibrium constant (kex) for the above reaction was calculated to be 10-2.26. The extraction process was endothermic in nature having positive DH value of 16.27 kJ/mol. The loading of D2EHPA by Zn(II) is about 4.50 g of Zn(II) by 0.10 M D2EHPA. Possible reaction mechanism has been suggested based on distribution data, extractant concentration and equilibrium pH of the aqueous phase. (author)

Advanced Aqueous Separation Systems for Actinide Partitioning

Energy Technology Data Exchange (ETDEWEB)

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

2015-04-02

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

Solubility and stability of dalcetrapib in vehicles and biological media.

Science.gov (United States)

Gross, Günter; Tardio, Joseph; Kuhlmann, Olaf

2012-11-01

Dalcetrapib solubility was determined in aqueous and in non-aqueous vehicles and in biorelevant media. In a pure aqueous environment the solubility was low but could be increased by addition of surfactants or complexing agents. This was also reflected in the solubility seen in simulated gastrointestinal (GI) fluids, with almost no solubility in simulated gastric fluid, but reasonable solubilisation in simulated intestinal fluids containing lecithin and bile salt. Additionally, the stability of dalcetrapib was determined in simulated GI fluids with and without pancreatic lipase. In solutions without lipase, dalcetrapib was slowly hydrolysed, but in the presence of lipase the hydrolysis rate was significantly faster depending on pH and enzyme activity. In biological fluids, dissolved dalcetrapib appeared to behave similarly being rapidly hydrolysed in human intestinal fluids with a half-life below 20s with no degradation observed in human gastric fluids at low pH. The results provide supportive evidence that absorption is higher under fed conditions and indicate lipase inhibitors might interfere with oral absorption of dalcetrapib. Copyright © 2012 Elsevier B.V. All rights reserved.

Electrochemical detection of copper ions leached from CuO nanoparticles in saline buffers and biological media using a gold wire working electrode

Energy Technology Data Exchange (ETDEWEB)

Baldisserri, Carlo, E-mail: carlo.baldisserri@istec.cnr.it; Costa, Anna Luisa [ISTEC-CNR (Italy)

2016-04-15

We performed explorative cyclic voltammetry in phosphate-buffered saline buffers, Dulbecco’s modified Eagle’s medium (DMEM), and fetal bovine serum-added DMEM using Au wire as working electrode, both in the absence and in the presence of known nominal concentrations of Cu{sup 2+} ions or 15 nm CuO nanoparticles. Addition of either Cu{sup 2+} ions or aqueous suspension of CuO nanoparticles caused a single anodic peak to appear in the double-layer region of all three pristine media. The height of the anodic peak was found to increase in a monotonic fashion vs. Cu{sup 2+} concentration in Cu{sup 2+}-added media, and versus time since CuO addition in CuO-added media. Stepwise addition of glycine to Cu{sup 2+}-added phosphate-buffered saline buffer caused an increasing cathodic shift of the anodic peak accompanied by decreasing peak currents. Results indicate that preparing Cu{sup 2+}-free suspensions of CuO nanoparticles in such media is difficult, owing to the presence of leached copper ions. The implications on results of experiments in which CuO nanoparticle-added biological media are used as cell culture substrates are discussed. Literature data on the interactions between Cu{sup 2+} ions, dissolved carbon dioxide in aqueous CuO suspensions, and amino acids present in such media are compared to our results.

Electrochemical detection of copper ions leached from CuO nanoparticles in saline buffers and biological media using a gold wire working electrode

Science.gov (United States)

Baldisserri, Carlo; Costa, Anna Luisa

2016-04-01

We performed explorative cyclic voltammetry in phosphate-buffered saline buffers, Dulbecco's modified Eagle's medium (DMEM), and fetal bovine serum-added DMEM using Au wire as working electrode, both in the absence and in the presence of known nominal concentrations of Cu2+ ions or 15 nm CuO nanoparticles. Addition of either Cu2+ ions or aqueous suspension of CuO nanoparticles caused a single anodic peak to appear in the double-layer region of all three pristine media. The height of the anodic peak was found to increase in a monotonic fashion vs. Cu2+ concentration in Cu2+-added media, and versus time since CuO addition in CuO-added media. Stepwise addition of glycine to Cu2+-added phosphate-buffered saline buffer caused an increasing cathodic shift of the anodic peak accompanied by decreasing peak currents. Results indicate that preparing Cu2+-free suspensions of CuO nanoparticles in such media is difficult, owing to the presence of leached copper ions. The implications on results of experiments in which CuO nanoparticle-added biological media are used as cell culture substrates are discussed. Literature data on the interactions between Cu2+ ions, dissolved carbon dioxide in aqueous CuO suspensions, and amino acids present in such media are compared to our results.

Radiation crosslinking of methylcellulose and hydroxyethylcellulose in concentrated aqueous solutions

International Nuclear Information System (INIS)

Wach, Radoslaw A.; Mitomo, Hiroshi; Nagasawa, Naotsugu; Yoshii, Fumio

2003-01-01

The effects of ionizing radiation on aqueous solutions of cellulose ethers, methylcellulose (MC) and hydroxyethylcellulose (HEC) were investigated. The well-established knowledge states that cellulose and its derivatives belong to degrading type of polymers. However, in our study intermolecular crosslinking initiated by gamma rays or electron beam leaded to the formation of insoluble gel. This is an opposite effect of irradiation to the degradation. Paste-like form of the initial specimen, i.e. concentration 20-30%, when water plasticizes the bulk of polymer; and a high dose rate were favorable for hydrogel formation. Gel fraction up to 60% and 70% was obtained from solutions of HEC and MC, respectively. Produced hydrogels swell markedly in aqueous media by imbibing and holding the solvent. Radiation parameters of irradiation, such as yields of degradation and crosslinking and the gelation dose, were evaluated by sol-gel analysis on the basis of Charlesby-Rosiak equation. Despite of the crosslinked structure, obtained hydrogels can be included into the group of biodegradable materials. They undergo decomposition by the action of cellulase enzyme or microorganisms from compost

Flow of Aqueous Humor

Science.gov (United States)

... Home Flow of Aqueous Humor Flow of Aqueous Humor Most, but not all, forms of glaucoma are ... remains normal when some of the fluid (aqueous humor) produced by the eye's ciliary body flows out ...

A unidirectional acoustic cloak for multilayered background media with homogeneous metamaterials

International Nuclear Information System (INIS)

Zhu, Jian; Chen, Tianning; Liang, Qingxuan; Wang, Xiaopeng; Xiong, Jie; Jiang, Ping

2015-01-01

The acoustic cloak, which can make an object hard to detect acoustically in a homogeneous background, has attracted great attention from researchers in recent years. The inhomogeneous background media were considered in this paper. The relative constitutive parameters were derived for acoustic cloaks working in multilayered media. And a unidirectional acoustic cloak for layered background media was proposed, designed and implemented successfully in a wide frequency range. In water and NaCl aqueous solution, the acoustic cloak was designed and realized with homogeneous metamaterials which were composed of steel and porous materials. The effective parameters of the unit cells of the cloak were determined by using the effective medium theory. Numerical results demonstrated excellent cloaking performance and showed that such a device could be physically realized with natural materials which will greatly promote the real applications of an invisibility cloak in inhomogeneous backgrounds. (paper)

Dynamics of Coupled Contaminant and Microbial Transport in Heterogeneous Porous Media: Purdue Component

Energy Technology Data Exchange (ETDEWEB)

Cushman, J.H.; Madilyn Fletcher

2000-06-01

Dynamic microbial attachment/detachment occurs in subsurface systems in response to changing environmental conditions caused by contaminant movement and degradation. Understanding the environmental conditions and mechanisms by which anaerobic bacteria partition between aqueous and solid phases is a critical requirement for designing and evaluating in situ bioremediation efforts. This interdisciplinary research project, of which we report only the Purdue contribution, provides fundamental information on the attachment/detachment dynamics of bacteria in heterogeneous porous media. Fundamental results from the Purdue collaboration are: (a) development of a matched-index method for obtaining 3-D Lagrangian trajectories of microbial sized particles transporting within porous media or microflow cells, (b) application of advanced numerical methods to optimally design a microflow cell for studying anaerobic bacterial attachment/detachment phenomena, (c) development of two types of models for simulating bacterial movement and attachment/detachment in microflow cells and natural porous media, (d) application of stochastic analysis to upscale pore scale microbial attachment/detachment models to natural heterogeneous porous media, and (e) evaluation of the role nonlocality plays in microbial dynamics in heterogeneous porous media

Dynamics of Coupled Contaminant and Microbial Transport in Heterogeneous Porous Media: Purdue Component

Energy Technology Data Exchange (ETDEWEB)

Cushman, J.H.

2000-06-01

Dynamic microbial attachment/detachment occurs in subsurface systems in response to changing environmental conditions caused by contaminant movement and degradation. Understanding the environmental conditions and mechanisms by which anaerobic bacteria partition between aqueous and solid phases is a critical requirement for designing and evaluating in situ bioremediation efforts. This interdisciplinary research project, of which we report only the Purdue contribution, provides fundamental information on the attachment/detachment dynamics of bacteria in heterogeneous porous media. Fundamental results from the Purdue collaboration are: (a) development of a matched-index method for obtaining 3-D Lagrangian trajectories of microbial sized particles transporting within porous media or microflow cells, (b) application of advanced numerical methods to optimally design a microflow cell for studying anaerobic bacterial attachment/detachment phenomena, (c) development of two types of models for simulating bacterial movement and attachment/detachment in microflow cells and natural porous media, (d) application of stochastic analysis to upscale pore scale microbial attachment/detachment models to natural heterogeneous porous media, and (e) evaluation of the role nonlocality plays in microbial dynamics in heterogeneous porous media.

Delamination of hexagonal boron nitride in a stirred media mill

International Nuclear Information System (INIS)

Damm, C.; Körner, J.; Peukert, W.

2013-01-01

A scalable process for delamination of hexagonal boron nitride in an aqueous solution of the non-ionic surfactant TWEEN85 using a stirred media mill is presented. The size of the ZrO 2 beads used as grinding media governs the dimensions of the ground boron nitride particles as atomic force microscopic investigations (AFM) reveal: the mean flakes thickness decreases from 3.5 to 1.5 nm and the ratio between mean flake area and mean flake thickness increases from 2,200 to 5,800 nm if the grinding media size is reduced from 0.8 to 0.1 mm. This result shows that a high number of stress events in combination with low stress energy (small grinding media) facilitate delamination of the layered material whereas at high stress energies in combination with a low number of stress events (large grinding media) breakage of the layers dominates over delamination. The results of particle height analyses by AFM show that few-layer structures have been formed by stirred media milling. This result is in agreement with the layer thickness dependence of the delamination energy for hexagonal boron nitride. The concentration of nanoparticles remaining dispersed after centrifugation of the ground suspension increases with grinding time and with decreasing grinding media size. After 5 h of grinding using 0.1 mm ZrO 2 grinding media the yield of nanoparticle formation is about 5 wt%. The nanoparticles exhibit the typical Raman peak for hexagonal boron nitride at 1,366 cm −1 showing that the in-plane order in the milled platelets is remained.

Practical and mechanistic aspects of the removal of cadmium from aqueous systems using peat

International Nuclear Information System (INIS)

Fine, Pinchas; Scagnossi, Alessandra; Chen, Yona; Mingelgrin, Uri

2005-01-01

A sphagnum peat moss removed Cd from aqueous solutions very efficiently, and its effectiveness in taking up the metal was significantly enhanced by exposure to a 1 N NaOH solution. The capacity of the untreated peat for Cd reached 300 g/kg and that of the NaOH-activated peat was over 400 g/kg. Although saturation was rarely reached, the Cd uptake from concentrated solutions often exceeded 200 g/kg. In column experiments, 1 g of the NaOH-activated peat completely removed the metal from over 0.2 L of a 200-mg/L Cd solution (final Cd concentration c /kg. In addition to uptake by exchange, a significant amount of Cd was sorbed by non-exchange mechanisms. FTIR spectroscopy revealed the importance of carboxyl groups in the uptake. - Peat can efficiently remove transition metals from aqueous media

Use of aqueous and solvent extraction to assess risk and bioavailability of contaminated soil

International Nuclear Information System (INIS)

Bordelon, N.; Huebner, H.; Washburn, K.; Donnelly, K.C.

1995-01-01

Contaminated media at Superfund sites typically consist of complex mixtures of organic and inorganic chemicals. These mixtures are difficult to characterize, both analytically and toxicologically, especially the complex mixtures of polycyclic aromatic hydrocarbons. The current approach to risk assessment assumes that all contaminants in the soil are available for human exposure. EPA protocol uses solvent extraction to remove chemicals from the soil as a basis for estimating risk to the human population. However, contaminants that can be recovered with a solvent extract may not represent chemicals that are available for exposure. A system using aqueous extraction provides a more realistic picture of what chemicals are bioavailable through leaching and ingestion. A study was conducted with coal tar contaminated soil spiked with benzo(a)pyrene, and trinitrotoluene. Samples were extracted with hexane:acetone and water titrated to pH 2 and pH 7. HPLC analysis demonstrated up to 35% and 29% recovery of contaminants from aqueous extracts with an estimated cancer risk one order of magnitude less than that for solvent extracts. Analysis using the Salmonella/microsome assay showed that solvent extracts were genotoxic with metabolic activation while aqueous extracts showed no genotoxicity. These results suggest that aqueous extraction may be useful in determining what contaminants are available for human exposure, as well as what compounds may pose a risk to human health

A simple, reversible, colorimetric and water-soluble fluorescent chemosensor for the naked-eye detection of Cu2 + in 100% aqueous media and application to real samples

Science.gov (United States)

Sun, Tao; Niu, Qingfen; Li, Tianduo; Guo, Zongrang; Liu, Haixia

2018-01-01

A simple, reversible, colorimetric and water-soluble fluorescent chemosensor ADA for the naked-eye detection of Cu2 + was developed. Sensor ADA showed high selectivity and sensitivity toward Cu2 + in 100% aqueous media over wide pH range. Sensor ADA exhibited a red-shift in the absorption spectra from 466 to 480 nm that is accompanied by significant color change from light yellow to yellowish brown instantaneously. The Cu2 + recognition is based on the chelation-enhanced fluorescence quenching (CHEQ) effect of the paramagnetic nature. The lowest detection limit is determined to be 15.8 nM, which is much lower than the allowable level of Cu2 + in drinking water set by U.S. Environmental Protection Agency ( 20 μM) and the World Health Organization ( 30 μM). The 1:1 binding process was confirmed by fluorescence measurements, IR analysis and DFT studies. Moreover, sensor ADA was successfully applied for determination of trace level of Cu2 + with 4 reuse cycles in various water samples, which affords promising potential in ion-detection field.

Recovery of metals from simulant spent lithium-ion battery as organophosphonate coordination polymers in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Perez, Emilie; Andre, Marie-Laure; Navarro Amador, Ricardo [ICSM, Institut de Chimie Séparative de Marcoule, UMR 5257, CEA/CNRS/ENSCM/UM, Bât 426, BP 17171, 30207 Bagnols-sur-Cèze cedex (France); Hyvrard, François; Borrini, Julien [SARPI VEOLIA, Direction Technique et Innovations, Zone portuaire de Limay-Porcheville, 427 route du Hazay, 78520 Limay (France); Carboni, Michaël, E-mail: michael.carboni@cea.fr [ICSM, Institut de Chimie Séparative de Marcoule, UMR 5257, CEA/CNRS/ENSCM/UM, Bât 426, BP 17171, 30207 Bagnols-sur-Cèze cedex (France); Meyer, Daniel [ICSM, Institut de Chimie Séparative de Marcoule, UMR 5257, CEA/CNRS/ENSCM/UM, Bât 426, BP 17171, 30207 Bagnols-sur-Cèze cedex (France)

2016-11-05

Highlights: • Original waste disposal strategies for battery. • Precipitation of metals as coordination polymers. • Organo-phosphonate coordination polymers. • Selective extraction of manganese or co-precipitation of manganese/cobalt. • The recycling process give a promising application on any waste solution. - Abstract: An innovative approach is proposed for the recycling of metals from a simulant lithium-ion battery (LIBs) waste aqueous solution. Phosphonate organic linkers are introduced as precipitating agents to selectively react with the metals to form coordination polymers from an aqueous solution containing Ni, Mn and Co in a hydrothermal process. The supernatant is analyzed by ICP-AES to quantify the efficiency and the selectivity of the precipitation and the materials are characterized by Scanning Electron Microscopy (SEM), Powder X-Ray Diffraction (PXRD), Thermogravimetric Analyses (TGA) and nitrogen gas sorption (BET). Conditions have been achieved to selectively precipitate Manganese or Manganese/Cobalt from this solution with a high efficiency. This work describes a novel method to obtain potentially valuable coordination polymers from a waste metal solution that can be generalized on any waste solution.

Effects of self-aggregation on the hydration of an amphiphilic antidepressant drug in different aqueous media

International Nuclear Information System (INIS)

Taboada, Pablo; Gutierrez-Pichel, Manuel; Mosquera, Victor

2004-01-01

Apparent molal volumes and adiabatic compressibilities of aqueous solutions of the amphiphilic antidepressant drug clomipramine hydrochloride have been determined from density and ultrasound velocity measurements in the temperature range 288.15-313.15 K in buffered aqueous solution of pH 3.0 and 5.5. Critical concentrations of aggregation of this drug were obtained from inflections on the plots of the sound velocity against drug concentration. Apparent molal adiabatic compressibilities of the aggregates formed by the drug, calculated by combining the ultrasound velocity and density data, were typical of those for a stacked aggregate. From the temperature dependence of the critical concentration and using the mass action model combined with the Phillips definition of the critical concentration the thermodynamic standard quantities: free Gibbs energy, enthalpy and entropy of aggregate formation were calculated. The critical concentration and energy involved in the aggregation process of this drug have been also evaluated experimentally using isothermal titration calorimetry at 298.15 K. The solvent-drug interactions have been discussed from compressibility and calorimetry data

Disposal of heavy metal cations in aqueous media by adsorption on coal to Ghazni

Directory of Open Access Journals (Sweden)

О.М. Заславський

2008-03-01

Full Text Available  Adsorption of Pb and Cu cations and their mixture on the surface of modified and non-modified anti-gas coal trough different time intervals have been studied. The maximum adsorption capacity of coal relative to each cations have been determined. Absence  of concurrence between cations of Pb and Cu during adsorption from mixture is explained by difference of  types of their interaction with coal surface. The high effectiveness and perspectivities of application of anti-gas coal for neutralization of heavy metal cations in aqueous solution was shown.

Non-aqueous metathesis as a general approach to prepare nanodispersed materials: Case study of scheelites

International Nuclear Information System (INIS)

Afanasiev, Pavel

2015-01-01

A general approach to the preparation of inorganic nanoparticles is proposed, using metathesis of precursor salts in non-aqueous liquids. Nanoparticles of scheelites AMO 4 (A=Ba, Sr, Ca; M=Mo, W), were obtained with a quantitative yield. Precipitations in formamide, N-methylformamide, propylene carbonate, DMSO and polyols often provide narrow particle size distributions. Advantageous morphology was explained by strong ionic association in non-aqueous solvents, leading to slow nucleation and negligible Ostwald ripening. Mean particle size below 10 nm and high specific surface areas were obtained for several Ca(Sr)Mo(W)O 4 materials, making them promising for applications as adsorbents or catalysts. Zeta-potential of scheelites in aqueous suspensions showed negative values in a wide range of pH. Systematic study of optical properties demonstrated variation of optical gap in the sequences W>Mo and Ba>Sr>Ca. The observed trends were reproduced by DFT calculations. No quantum confinement effect was observed for small particles, though the surface states induce low-energy features in the optical spectra. - Graphical abstract: Scheelites AMO 4 (A=Ca, Sr, Ba; M=Mo, W) were prepared in various non-aqueous liquids with high specific surface areas and narrow size distributions. The optical gap of scheelites changes in the series Caaqueous liquids. • Narrow size distributions explained by ionic association in non-aqueous media. • Nanoparticles of less than 10 nm size and highest ever specific surface areas were obtained. • Optical gap of scheelites changes in the series Ca

A sigmoidal model for biosorption of heavy metal cations from aqueous media.

Science.gov (United States)

Özen, Rümeysa; Sayar, Nihat Alpagu; Durmaz-Sam, Selcen; Sayar, Ahmet Alp

2015-07-01

A novel multi-input single output (MISO) black-box sigmoid model is developed to simulate the biosorption of heavy metal cations by the fission yeast from aqueous medium. Validation and verification of the model is done through statistical chi-squared hypothesis tests and the model is evaluated by uncertainty and sensitivity analyses. The simulated results are in agreement with the data of the studied system in which Schizosaccharomyces pombe biosorbs Ni(II) cations at various process conditions. Experimental data is obtained originally for this work using dead cells of an adapted variant of S. Pombe and represented by Freundlich isotherms. A process optimization scheme is proposed using the present model to build a novel application of a cost-merit objective function which would be useful to predict optimal operation conditions. Copyright © 2015. Published by Elsevier Inc.

Aqueous Extracts of Hibiscus sabdariffa Calyces to Control Aichi Virus.

Science.gov (United States)

D'Souza, Doris H; Dice, Lezlee; Davidson, P Michael

2016-06-01

Aqueous Hibiscus sabdariffa extracts possess antimicrobial properties with limited information available on their antiviral effects. Aichi virus (AiV) is an emerging foodborne pathogen that causes gastroenteritis. Vaccines are currently unavailable to prevent their disease transmission. The objective of this study was to determine the antiviral effects of aqueous H. sabdariffa extracts against AiV. AiV at ~5 log PFU/ml was incubated with undiluted (200 mg/ml), 1:1 (100 mg/ml) or 1:5 (40 mg/ml) diluted aqueous hibiscus extract (pH 3.6), phosphate-buffered saline (pH 7.2 as control), or malic acid (pH 3.0, acid control) at 37 °C over 24 h. Treatments were stopped by serially diluting in cell-culture media containing fetal bovine serum and titers were determined using plaque assays on confluent Vero cells. Each treatment was replicated thrice and assayed in duplicate. AiV did not show any significant reduction with 1:1 (100 mg/ml) or 1:5 (40 mg/ml) diluted aqueous hibiscus extracts or malic acid after 0.5, 1, or 2 h at 37 °C. However, AiV titers were reduced to non-detectable levels after 24 h with all the three tested concentrations, while malic acid showed only 0.93 log PFU/ml reduction after 24 h. AiV was reduced by 0.5 and 0.9 log PFU/ml with undiluted extracts (200 mg/ml) after 2 and 6 h, respectively. AiV treated with 1:1 (100 mg/ml) and 1:5 (40 mg/ml) diluted extracts showed a minimal ~0.3 log PFU/ml reduction after 6 h. These extracts show promise to reduce AiV titers mainly through alteration of virus structure, though higher concentrations may have improved effects.

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

Energy Technology Data Exchange (ETDEWEB)

Rogers, Robin D

2007-06-25

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

Rhodamine B immobilized on hollow Au-HMS material for naked-eye detection of Hg{sup 2+} in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Zhang, Na [State Key Laboratory of Fine Chemicals, College of Chemical Engineering, Dalian University of Technology, Dalian, 116024 (China); Li, Gang, E-mail: liganghg@dlut.edu.cn [State Key Laboratory of Fine Chemicals, College of Chemical Engineering, Dalian University of Technology, Dalian, 116024 (China); Cheng, Zhuhong [State Key Laboratory of Fine Chemicals, College of Chemical Engineering, Dalian University of Technology, Dalian, 116024 (China); Zuo, Xiujin [Key Laboratory of Bio-organic Chemistry, College of Environmental and Chemical Engineering, Dalian University, Dalian, 116622 (China)

2012-08-30

Graphical abstract: Au-HMS-Probe with worm-like mesoporous framework for detection of Hg{sup 2+} in aqueous media has been simply and effectively synthesized by immobilizing a Rhodamine B derivative on Au-HMS via Au-N groups under room temperature. Highlights: Black-Right-Pointing-Pointer Au-HMS-Probe is prepared via Au-N bonds. Black-Right-Pointing-Pointer Gold nanoparticles are chosen as connectors instead of silane agents. Black-Right-Pointing-Pointer Au-HMS is chosen as carrier for the first time. Black-Right-Pointing-Pointer The immobilization method of Au-HMS-Probe is very simple and effective. Black-Right-Pointing-Pointer Au-HMS-Probe shows excellent ability for detecting Hg{sup 2+} by naked-eye. - Abstract: A simple, effective method has been demonstrated to immobilize Rhodamine B (RhB) probes on mesoporous silica (Au-HMS). The prepared chemosensor (Au-HMS-Probe) was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD), UV-vis spectrum and Fourier transform infrared spectroscopy (FT-IR). Further application of Au-HMS-Probe in sensing Hg{sup 2+} was confirmed by fluorescence titration experiment. Au-HMS-Probe afforded 'turn-on' fluorescence enhancement and displayed high brightness in water, and it also showed excellent selectivity for Hg{sup 2+} over alkali (Na{sup +}, K{sup +}), alkaline earth (Mg{sup 2+}, Ca{sup 2+}) and other heavy metal ions (Ag{sup +}, Cd{sup 2+}, Co{sup 2+}, Pb{sup 2+}, Ni{sup 2+}, Cu{sup 2+}, Fe{sup 2+}). Importantly, Au-HMS-Probe could be regenerated by treatment with tetrapropylammonium hydroxide solution.

Facile synthesis of “green” gold nanocrystals using cynarin in an aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Katircioğlu, Zeynep; Şakalak, Hüseyin [Department of Metallurgical and Materials Engineering, Selcuk University, Konya 42075 (Turkey); Nanobiotechnology Laboratory, Advanced Technology Research and Application Center, Selcuk University, Konya 42075 (Turkey); Ulaşan, Mehmet [Nanobiotechnology Laboratory, Advanced Technology Research and Application Center, Selcuk University, Konya 42075 (Turkey); Department of Chemistry, Selcuk University, Konya 42075 (Turkey); Gören, Ahmet Ceyhan, E-mail: ahmetceyhan.goren@tubitak.gov.tr [TÜBİTAK UME, Chemistry Group, Organic Chemistry Laboratories, 41470 Gebze, Kocaeli (Turkey); Yavuz, Mustafa Selman, E-mail: selmanyavuz@selcuk.edu.tr [Department of Metallurgical and Materials Engineering, Selcuk University, Konya 42075 (Turkey); Nanobiotechnology Laboratory, Advanced Technology Research and Application Center, Selcuk University, Konya 42075 (Turkey)

2014-11-01

Highlights: • The first time a remarkably simple, versatile, environmentally friendly, one-pot and biogenic fabrication and aqueous synthesis of monodisperse gold nanoparticles by using cynarin. • Cynarin as a reductant and capping agent. • Exclusion of extra reducing agents or reductant. • Fabrication of Pd and Ag nanoparticles using cynarin in aqueous media. - Abstract: Herein we describe a water-based protocol that generates Au nanoparticles (AuNPs) by mixing aqueous solutions of HAuCl4 and cynarin (a natural product extract from artichoke leaf). Based on the observations from {sup 1}H NMR spectrum of AuNPs, a polyol oxidation mechanism by metal ions which eventually results in AuNPs formation, is proposed. Basically, the aromatic alcohol groups (1,2-benzenediol) of cynarin are oxidized to α-hydroxy ketone intermediate product, and then further oxidized to the vicinal diketone final product while the Au{sup 3+} ions are reduced to its atomic form (Au{sup 0}) which leads the generation of Au nanoparticles. This new protocol has also been employed to prepare multiply twinned Pd nanoparticles and Ag cubical aggregates. Due to exclusion of organic solvent, surfactant, or stabilizer for all these synthesis, this protocol may provide a simple, versatile, and environmentally benign route to fabricate noble-metal nanoparticles having various compositions and morphologies.

Facile synthesis of “green” gold nanocrystals using cynarin in an aqueous solution

International Nuclear Information System (INIS)

Katircioğlu, Zeynep; Şakalak, Hüseyin; Ulaşan, Mehmet; Gören, Ahmet Ceyhan; Yavuz, Mustafa Selman

2014-01-01

Highlights: • The first time a remarkably simple, versatile, environmentally friendly, one-pot and biogenic fabrication and aqueous synthesis of monodisperse gold nanoparticles by using cynarin. • Cynarin as a reductant and capping agent. • Exclusion of extra reducing agents or reductant. • Fabrication of Pd and Ag nanoparticles using cynarin in aqueous media. - Abstract: Herein we describe a water-based protocol that generates Au nanoparticles (AuNPs) by mixing aqueous solutions of HAuCl4 and cynarin (a natural product extract from artichoke leaf). Based on the observations from 1 H NMR spectrum of AuNPs, a polyol oxidation mechanism by metal ions which eventually results in AuNPs formation, is proposed. Basically, the aromatic alcohol groups (1,2-benzenediol) of cynarin are oxidized to α-hydroxy ketone intermediate product, and then further oxidized to the vicinal diketone final product while the Au 3+ ions are reduced to its atomic form (Au 0 ) which leads the generation of Au nanoparticles. This new protocol has also been employed to prepare multiply twinned Pd nanoparticles and Ag cubical aggregates. Due to exclusion of organic solvent, surfactant, or stabilizer for all these synthesis, this protocol may provide a simple, versatile, and environmentally benign route to fabricate noble-metal nanoparticles having various compositions and morphologies

Predicting Upscaled Behavior of Aqueous Reactants in Heterogeneous Porous Media

Science.gov (United States)

Wright, E. E.; Hansen, S. K.; Bolster, D.; Richter, D. H.; Vesselinov, V. V.

2017-12-01

When modeling reactive transport, reaction rates are often overestimated due to the improper assumption of perfect mixing at the support scale of the transport model. In reality, fronts tend to form between participants in thermodynamically favorable reactions, leading to segregation of reactants into islands or fingers. When such a configuration arises, reactions are limited to the interface between the reactive solutes. Closure methods for estimating control-volume-effective reaction rates in terms of quantities defined at the control volume scale do not presently exist, but their development is crucial for effective field-scale modeling. We attack this problem through a combination of analytical and numerical means. Specifically, we numerically study reactive transport through an ensemble of realizations of two-dimensional heterogeneous porous media. We then employ regression analysis to calibrate an analytically-derived relationship between reaction rate and various dimensionless quantities representing conductivity-field heterogeneity and the respective strengths of diffusion, reaction and advection.

MIPs in Aqueous Environments.

Science.gov (United States)

Wan, Ying-chun; Ma, Hui-ting; Lu, Bin

2015-01-01

When organic solvent-compatible molecularly imprinted polymers (MIPs) are used in aqueous environment, how to reduce nonspecific binding is a major challenge. By modifying the binding solvents and introducing appropriate washing and elution steps, even relatively hydrophobic MIPs can gain optimal rebinding selectivity in aqueous conditions. Furthermore, water-compatible MIPs that can be used to treat aqueous samples directly have been prepared. The use of hydrophilic co-monomers, the controlled surface modification through controlled radical polymerization, and the new interfacial molecular imprinting methods are different strategies to prepare water-compatible MIPs. By combining MIPs with other techniques, both organic solvent-compatible and water-compatible MIPs can display better functional performances in aqueous conditions. Intensive studies on MIPs in aqueous conditions can provide new MIPs with much-improved compatibilities that will lead to more interesting applications in biomedicine and biotechnology.

Spectral characteristics and colloidal properties of chlorophyll a{prime} in aqueous methanol

Energy Technology Data Exchange (ETDEWEB)

Oba, Toru [Ritsumeikan Univ., Kusatsu (Japan); Mimuro, Mamoru [National Inst. for Basic Biology, Okazaki (Japan); Wang, Z.Y.; Nozawa, Tsunenori [Tohoku Univ., Sendai (Japan); Yoshida, Shoichiro; Watanabe, Tadashi [Univ. of Tokyo (Japan)

1997-04-17

The `phase behavior` of chlorophyll a` (Chl a`, C13{sup 2}-epimer of Chl a) dissolved in aqueous methanol was examined in terms of the composition of the solvent. The study aimed at elucidating the property of Chl a`, the exotic pigment found in a photosynthetic reaction center complex, as well as at clarifying the nature of the Chl aggregation in aqueous media. Visible absorption, circular dichroism (CD), fluorescence and resonance Raman spectroscopies, dynamic light-scattering measurements, and electron microscopy were utilized. Chl a` formed either of two types of colloids depending on the solvent composition. The one formed over a wide methanol volume percentage (ca. 73-30%) commonly possessed a single microscopic structural unit that yielded the double-peaked absorption (ca. 690 and 715 nm) accompanied by a symmetric dispersed-type CD spectrum. Increasing methanol concentration within this solvent composition range enhanced the size of the colloid and finally caused critical opalescence, which was reminiscent of the critical behavior of the aqueous solution of nonionic surfactants. These findings indicate that the microscopic structure of the Chl a` aggregate was independent of the size and shape of the colloid. The difference between the aggregation behaviors of Chl a and a` suggests a narrower choice of possible molecular arrangements in the Chl a` aggregate as an inherent property of the pigment. 37 refs., 11 figs.

Aqueous electrolytes for redox flow battery systems

Science.gov (United States)

Liu, Tianbiao; Li, Bin; Wei, Xiaoliang; Nie, Zimin; Wang, Wei; Liu, Jun; Sprenkle, Vincent L.

2017-10-17

An aqueous redox flow battery system includes an aqueous catholyte and an aqueous anolyte. The aqueous catholyte may comprise (i) an optionally substituted thiourea or a nitroxyl radical compound and (ii) a catholyte aqueous supporting solution. The aqueous anolyte may comprise (i) metal cations or a viologen compound and (ii) an anolyte aqueous supporting solution. The catholyte aqueous supporting solution and the anolyte aqueous supporting solution independently may comprise (i) a proton source, (ii) a halide source, or (iii) a proton source and a halide source.

Injection of colloidal size particles of Fe0 in porous media with shearthinning fluids as a method to emplace a permeable reactive zone

International Nuclear Information System (INIS)

Cantrell, K.J.; Kaplan, D.I.; Gilmore, T.J.

1997-01-01

Previous work has demonstrated the feasibility of injecting suspensions of micron-size zero-valent (FeO) particles into porous media as a method to emplace a permeable reactive zone. Further studies were conducted to evaluate the effects of several shearthinning fluids on enhancing the injectability of micron-size FeO particles into porous media. In contrast to Newtonian fluids, whose viscosities are constant with shear rate, certain non-Newtonian fluids are shearthinning, that is, the viscosity of these fluids decreases with increasing shear rate. The primary benefit of using these fluids for this application is that they increase the viscosity of the aqueous phase without adversely decreasing the hydraulic conductivity. A suspension formulated with a shearthinning fluid will maintain a relatively high viscosity in solution near the FeO particles (where the shear stress is low) relative to locations near the surfaces of the porous media, where the shear stress is high. The increased viscosity decreases the rate of gravitational settling of the dense FeO colloids (7.6 9/cm3) while maintaining a relatively high hydraulic conductivity that permits pumping the colloid suspensions into porous media at greater flowrates and distances. Aqueous solutions of three polymers at different concentrations were investigated. It was determined that, the use of shear thinning fluids greatly increases the injectability of the colloidal FeO suspensions in porous media

Conformation of poly(γ-glutamic acid) in aqueous solution.

Science.gov (United States)

Muroga, Yoshio; Nakaya, Asami; Inoue, Atsuki; Itoh, Daiki; Abiru, Masaya; Wada, Kaori; Takada, Masako; Ikake, Hiroki; Shimizu, Shigeru

2016-04-01

Local conformation and overall conformation of poly(γ-DL-glutamic acid) (PγDLGA) and poly(γ-L-glutamic acid) (PγLGA) in aqueous solution was studied as a function of degree of ionization ε by (1) H-NMR, circular dichroism, and potentiometric titration. It was clarified that their local conformation is represented by random coil over an entire ε range and their overall conformation is represented by expanded random-coil in a range of ε > ε(*) , where ε(*) is about 0.3, 0.35, 0.45, and 0.5 for added-salt concentration of 0.02M, 0.05M, 0.1M, and 0.2M, respectively. In a range of ε acidic media. © 2015 Wiley Periodicals, Inc.

SINTESIS BIODISEL DARI MINYAK BIJI KARET DENGAN VARIASI SUHU DAN KONSENTRASI KOH UNTUK TAHAPAN TRANSESTERIFIKASI

Directory of Open Access Journals (Sweden)

Ratna Dewi Kusumaningtyas

2013-05-01

Full Text Available Bahan bakar yang paling banyak digunakan adalah bahan bakar diesel atau fatty acid methyl ester (FAME. Biodiesel berasal dari minyak nabati yang dapat diperbaharui, dapat dihasilkan secara periodik, dan mudah diperoleh. Pada penelitian ini digunakan minyak biji karet untuk sintesis FAME. Proses utama dalam pembuatan FAME adalah transesterifikasi. Penelitian ini mengkaji hasil optimum dari variasi konsentrasi katalis KOH dan suhu reaksi pada reaksi transesterifikasi. Preparasi minyak biji karet dengan menggunakan arang aktif granular diikuti dengan degumming. Reaksi esterifikasi dilaksanakan pada kondisi operasi 500 C selama 1 jam, katalis asam sulfat (98% sebesar 0,5% volume minyak, dan metanol sebesar 20% volume minyak. Reaksi transesterifikasi dilaksanakan selama 1 jam, serta perbandingan volume minyak dan metanol sebesar 4:1. Analisis kadar metil ester yang terbentuk, jumlah komponen, dan komposisinya yang terdapat pada senyawa hasil dilakukan dengan menggunakan alat GC. Kondisi operasi terbaik pada transesterifikasi minyak biji karet menjadi metil ester adalah pada katalis KOH 1% dan suhu 60 0C. Berdasarkan uji sifat-sifat fisis, metil ester yang dihasilkan belum semua memenuhi mutu sifat fisis biodiesel yang disyaratkan. The most widely used fuel is diesel fuel or fatty acid methyl ester (FAME. Biodiesel is derived from vegetable oil that can be renewed, can be produced periodically, and easy to obtain. In this research, the rubber seed was used for synthesizing the FAME. The main process in the production of FAME is transesterification. This study examined the optimum result from variations of the concentration of KOH catalyst and the reaction temperature on the transesterification reaction. Preparation of the rubber seed oil using granular activated charcoal was followed by degumming. Esterification reaction was carried out at 50 oC for 1 h with the sulfuric acid catalyst of 0.5% by volume of oil and methanol of 20% by the volume of

Dynamics of Coupled Contaminant and Microbial Transport in Heterogeneous Porous Media: Purdue Component. Final report

International Nuclear Information System (INIS)

Cushman, J.H.

2000-01-01

Dynamic microbial attachment/detachment occurs in subsurface systems in response to changing environmental conditions caused by contaminant movement and degradation. Understanding the environmental conditions and mechanisms by which anaerobic bacteria partition between aqueous and solid phases is a critical requirement for designing and evaluating in situ bioremediation efforts. This interdisciplinary research project, of which we report only the Purdue contribution, provides fundamental information on the attachment/detachment dynamics of bacteria in heterogeneous porous media. Fundamental results from the Purdue collaboration are: (a) development of a matched-index method for obtaining 3-D Lagrangian trajectories of microbial sized particles transporting within porous media or microflow cells, (b) application of advanced numerical methods to optimally design a microflow cell for studying anaerobic bacterial attachment/detachment phenomena, (c) development of two types of models for simulating bacterial movement and attachment/detachment in microflow cells and natural porous media, (d) application of stochastic analysis to upscale pore scale microbial attachment/detachment models to natural heterogeneous porous media, and (e) evaluation of the role nonlocality plays in microbial dynamics in heterogeneous porous media

Effect of base media on the stability of annatto dye in industrial products

International Nuclear Information System (INIS)

Audetuyi, A.O.; Lajide, L.; Popoola, A.V.

2006-01-01

Colour stability of the versatile annatto dye was examined to monitor the effects of base media on industrial products. The dye was incorporated in two media, namely, palm kernel oil used in products such as body cream and soap, and paraffin wax used in shoe polish and household candle wax. These products were exposed to various light conditions for a specific period before assessment. The melting point of the dye was determined as 176-178 degree C with a molar absorptivity of 13,600 mol/sub -1/ cm/sub -1/ at 545 nm. It imparted its brilliant yellow/orange colouration in industrial products as the colour stability depends on the compounding base media of the products. Losses of beta-carotene was higher and faster in nonaqueous environment as paraffin wax showed low fastness rating values, than in the palm kernel oil based aqueous medium products. (author)

Contribution to the study of the behavior of tetravalent technetium at tracer amounts in aqueous media

International Nuclear Information System (INIS)

Guennec, J.Y.

The behavior of /sup 99m/Tc was studied first in perchloric media. Reduction of TcO 4 - by BH 4 - at pH 7 in perchloric medium leads to Tc(IV) as a radiocolloid (20 percent) and soluble TcO 2 (50 percent). Acidification of the medium oxidizes the soluble Tc(IV) fraction. Acid solutions containing only the IV species and free of radiocolloids can be studied using back extraction. Tc(IV) is extracted by the organic phases, containing or not containing TTA or HDEHP from solutions of Tc(VII) reduced by BH 4 - at pH 7. These organic phases are then contacted with aqueous phases 5 x 10 -2 to 3 M HClO 4 , and the variation of the distribution coefficient was studied as a function of the chelating agent content and of the pH. In the absence of a chelating agent, the extracted species is TcO 2 . In the presence of chelating agents, the cation TcO(OH) + is extracted in the forms TcO(OH)A and TcO(OH)A 2 H respectively with TTA and HDEHP. Hydrolysis of this cation leads to TcO 2 . Study of the reduction of Tc(VII) in hydrochloric medium is complicated by the oxychlorinated forms of Tc(IV). The hexachlorotechnetate ion, TcCl 6 , exists in HCl 12 M down to 1 M and is very inert. Addition of chloride ions to solutions containing only TcO 2 and TcO(OH) + , when [Cl - ] is less than 1 M, leads to a neutral extractable species, which could be TcOCl 2 . When the Cl - concentration is greater than 1 M, there is formation of a species with one more chlorine atoms; this could be TcOCl 3 . The behavior of technetium during the formation of the complex ''Tc-Iron-Ascorbic Acid'' used in medical scintigraphy was also studied. Ascorbic acid alone or divalent iron alone slightly reduce the pertechnetate. Addition of Fe 2+ (or BH 4 - ) to Tc(VII) and ascorbic acid produces a high percentage of Tc(IV). So it is the ascorbate of iron which reduces the Tc(VII) and the excess ascorbic acid maintains the technetium in its reduced state by formation of a weak complex

Extremophile mediated hydrogen production for hydrogenation of substrates in aqueous media

Science.gov (United States)

Anjom, Mouzhgun

Catalytic hydrogenation reactions are pervasive throughout our economy, from production of margarine as food, liquid fuels for transportation and chiral drugs such as L-DOPA. H2 production from non-fossil fuel feedstocks is highly desirable for transition to the "Hydrogen Economy". Also, the rates of hydrogenation reactions that involve a substrate, H 2 gas and a catalyst are often limited by the solubility of H2 in solvent. The present research thus envisioned designing water-soluble catalysts that could effectively utilize biologically produced H2 in a coupled system to hydrogenate substrates in homogeneous mode (two-phase system). Biological production of H2 as an end product or byproduct of the metabolism of organisms that operate under strict anaerobic conditions has been proposed. However, contrary to what was previously observed, Thermotoga neapolitana, belonging to the order of Thermotogales efficiently produces H2 gas under microaerobic conditions (Van Ooteghem et al. 2004). For H2 production by T. neapolitana in the bacterial growth medium (DSM 5068) at an optimum temperature of 70 C, our results in batch mode show that: (1) H2 was produced from glucose though with 16% efficiency, the rest goes to biomass production, (2) H2 gas was produced even when the cultures were inoculated under microaerobic conditions (up to 8% (v/v) O2) suggesting a protective mechanism for one or more [Fe-Fe] hydrogenases in T. neapolitana, (3) H2 production was pH dependent but addition of simple, non-toxic physiological buffering additives such as Methylene succinic acid increased H2 production and (4) H2 production rate varied linearly in the 100--6800 kPa pressure range. We then screened various water-soluble metal catalysts in batch mode and selected the RhCl3.3H2O/TPPTS (TPPTS is a water-soluble ligand) system that achieved 86% hydrogenation of Methylene succinic acid (an olefin) in an aqueous medium pressurized with preformed H2. When water was replaced with the DSM 5068

Progress in aqueous rechargeable batteries

OpenAIRE

Jilei Liu; Chaohe Xu; Zhen Chen; Shibing Ni; Ze Xiang Shen

2018-01-01

Over the past decades, a series of aqueous rechargeable batteries (ARBs) were explored, investigated and demonstrated. Among them, aqueous rechargeable alkali-metal ion (Li+, Na+, K+) batteries, aqueous rechargeable-metal ion (Zn2+, Mg2+, Ca2+, Al3+) batteries and aqueous rechargeable hybrid batteries are standing out due to peculiar properties. In this review, we focus on the fundamental basics of these batteries, and discuss the scientific and/or technological achievements and challenges. B...

On the importance of aqueous diffusion and electrostatic interactions in advection-dominated transport in saturated porous media

DEFF Research Database (Denmark)

Rolle, Massimo

2015-01-01

to multicomponent ionic dispersion: the dispersive fluxes of the different ions are cross-coupled due to the effects of Coulombic interactions. Such effects are illustrated in flow-through experiments in saturated porous media. Simple strong electrolytes were selected as tracers and their transport was studied...... under different advection-dominated conditions and in homogeneous and heterogeneous porous media. The interpretation of the experimental results requires a multicomponent modeling approach with an accurate description of local hydrodynamic dispersion and explicitly accounting for the cross-coupling...

A simple, reversible, colorimetric and water-soluble fluorescent chemosensor for the naked-eye detection of Cu2+ in ~100% aqueous media and application to real samples.

Science.gov (United States)

Sun, Tao; Niu, Qingfen; Li, Tianduo; Guo, Zongrang; Liu, Haixia

2018-01-05

A simple, reversible, colorimetric and water-soluble fluorescent chemosensor ADA for the naked-eye detection of Cu 2+ was developed. Sensor ADA showed high selectivity and sensitivity toward Cu 2+ in ~100% aqueous media over wide pH range. Sensor ADA exhibited a red-shift in the absorption spectra from 466 to 480nm that is accompanied by significant color change from light yellow to yellowish brown instantaneously. The Cu 2+ recognition is based on the chelation-enhanced fluorescence quenching (CHEQ) effect of the paramagnetic nature. The lowest detection limit is determined to be 15.8nM, which is much lower than the allowable level of Cu 2+ in drinking water set by U.S. Environmental Protection Agency (~20μM) and the World Health Organization (~30μM). The 1:1 binding process was confirmed by fluorescence measurements, IR analysis and DFT studies. Moreover, sensor ADA was successfully applied for determination of trace level of Cu 2+ with 4 reuse cycles in various water samples, which affords promising potential in ion-detection field. Copyright © 2017 Elsevier B.V. All rights reserved.

Aqueous lithium air batteries

Science.gov (United States)

Visco, Steven J.; Nimon, Yevgeniy S.; De Jonghe, Lutgard C.; Petrov, Alexei; Goncharenko, Nikolay

2017-05-23

Aqueous Li/Air secondary battery cells are configurable to achieve high energy density and prolonged cycle life. The cells include a protected a lithium metal or alloy anode and an aqueous catholyte in a cathode compartment. The aqueous catholyte comprises an evaporative-loss resistant and/or polyprotic active compound or active agent that partakes in the discharge reaction and effectuates cathode capacity for discharge in the acidic region. This leads to improved performance including one or more of increased specific energy, improved stability on open circuit, and prolonged cycle life, as well as various methods, including a method of operating an aqueous Li/Air cell to simultaneously achieve improved energy density and prolonged cycle life.

Detection of pollutants in aquatic media using a cell-based sensor

OpenAIRE

Guijarro Řezníček, Christian

2016-01-01

Water is a precious good which in good quality we need essentially to survive. In this work a novel method for the detection of bioactive pollutants in aqueous media will be presented. It is based on a sensor system, which uses mammalian cells, RLC-18 (rat liver cells) or MCF-7 (breast cancer cell line) as the detection layer for harmful substances. With these mammalian cells as the sensing layer a metabolically active sensor interface will become available reflecting the physiology of living...

Fluorescence-based detection of nitric oxide in aqueous and methanol media using a copper(II) complex.

Science.gov (United States)

Mondal, Biplab; Kumar, Pankaj; Ghosh, Pokhraj; Kalita, Apurba

2011-03-14

The quenched fluorescent intensity of a copper(II) complex, 1, of a fluorescent ligand, in degassed methanol or aqueous (buffered at pH 7.2) solution, was found to reappear on exposure to nitric oxide. Thus, it can function as a fluorescence based nitric oxide sensor. It has been found that the present complex can be used to sense nanomolar quantities of nitric oxide in both methanol and pH 7.2 buffered-water medium.

Highly selective probe based on imine linkage for Zn{sup 2+} and HSO{sub 3}{sup −} in mixed aqueous media

Energy Technology Data Exchange (ETDEWEB)

Kaur, Kamaljot; Chaudhary, Savita; Singh, Sukhjinder; Mehta, S.K., E-mail: skmehta@pu.ac.in

2015-04-15

A simple salicylaldehyde derived Schiff base N, N′- bis (p-chloro salicylidene)-1, 2- ethylenediamine (L) was synthesized and characterized. The receptor demonstrates simultaneous dual channel chromogenic and fluorogenic signaling towards HSO{sub 3}{sup −} and Zn{sup 2+} in mixed aqueous media. Solvatochromism was employed systematically for modulating its optoelectronic properties. The probe was successfully assessed to monitor HSO{sub 3}{sup −} detection via UV–vis spectroscopy. DFT calculations and {sup 1}H NMR spectroscopy further support the results based on shifting of equilibrium. Moreover, the sensor showed large fluorescence enhancement with blue-shift of 48 nm after addition of Zn{sup 2+}. The probe exhibits high selectivity over other competitive ions with high detection limit of 6.54×10{sup −5} M and 3.21×10{sup −6} M for HSO{sub 3}{sup −} and Zn{sup 2+}, respectively. Importantly, this is one of the rare reports in which Schiff base was utilized for the fabrication of chromogenic or fluorogenic sensor using solvent effect for multianalyte detection. - Highlights: • Easy synthesis of highly selective and sensitive Salicylideneaniline moiety. • Solvatochromism induced tautomerism between the enol-imine and keto-amine forms. • Computational studies revealing the effect of solvent on stability of NH form. • Discriminative detection of HSO{sub 3}{sup −} and Zn{sup 2+} by different spectroscopic techniques. • Optical feedbacks as absorption transitions with HSO{sub 3}{sup −} on bisulphite adduct formation. • Fluorescence enhancement for Zn{sup 2+} based on imine binding mechanism.

Lewis Acid Pairs for the Activation of Biomass-derived Oxygenates in Aqueous Media

Energy Technology Data Exchange (ETDEWEB)

Roman, Yuriy [Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States)

2015-09-14

The objective of this project is to understand the mechanistic aspects behind the cooperative activation of oxygenates by catalytic pairs in aqueous media. Specifically, we will investigate how the reactivity of a solid Lewis acid can be modulated by pairing the active site with other catalytic sites at the molecular level, with the ultimate goal of enhancing activation of targeted functional groups. Although unusual catalytic properties have been attributed to the cooperative effects promoted by such catalytic pairs, virtually no studies exist detailing the use heterogeneous water-tolerant Lewis pairs. A main goal of this work is to devise rational pathways for the synthesis of porous heterogeneous catalysts featuring isolated Lewis pairs that are active in the transformation of biomass-derived oxygenates in the presence of bulk water. Achieving this technical goal will require closely linking advanced synthesis techniques; detailed kinetic and mechanistic investigations; strict thermodynamic arguments; and comprehensive characterization studies of both materials and reaction intermediates. For the last performance period (2014-2015), two technical aims were pursued: 1) C-C coupling using Lewis acid and base pairs in Lewis acidic zeolites. Tin-, zirconium-, and hafnium containing zeolites (e.g., Sn-, Zr-, and Hf-Beta) are versatile solid Lewis acids that selectively activate carbonyl functional groups. In this aim, we demonstrate that these zeolites catalyze the cross-aldol condensation of aromatic aldehydes with acetone under mild reaction conditions with near quantitative yields. NMR studies with isotopically labeled molecules confirm that acid-base pairs in the Si-O-M framework ensemble promote soft enolization through α-proton abstraction. The Lewis acidic zeolites maintain activity in the presence of water and, unlike traditional base catalysts, in acidic solutions. 2) One-pot synthesis of MWW zeolite nanosheets for activation of bulky substrates. Through

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.)

Media Education Initiatives by Media Organizations: The Uses of Media Literacy in Hong Kong Media

Science.gov (United States)

Chu, Donna; Lee, Alice Y. L.

2014-01-01

As more media organizations have engaged in media education, this paper investigates the goals and practices of these activities. This article coins media education initiatives by media organizations with the term "media-organization media literac"y (MOML). Four MOML projects in Hong Kong were selected for examination. Built on critical…

Solvent extraction of hafnium(IV) by dinonylnaphthalene sulfonic acid from mixed aqueous-organic media

International Nuclear Information System (INIS)

Hala, J.; Piperkovova, H.

1979-01-01

The extraction of hafnium(IV) by heptane and toluene solutions of dinonylnaphthalene sulfonic acid (HD) from mixed aqueous-organic solutions has been studied. Alcohols, ketones, carboxylic acids, cyclic ethers, dimethylsulfoxide and dimethylformamide were used as the organic component of the mixed phase. Methanol, ethanol, formic acid and dioxane increased the extractability of Hf(IV) whereas other solvents showed only an antagonistic effect. The results were discussed from the point of view of the changes in micellar structure of HD, and compared with the uptake of Hf(IV) by resinous cation exchangers. The solubilization by HD of alcohols, carboxylic acids and dimethylsulfoxide was demonstrated by using the corresponding 14 C and 35 S labelled compounds. (author)

Fundamental investigation of the transport properties of superacids in aqueous and non-aqueous media

Science.gov (United States)

Suarez, Sophia

In the quest to develop more efficient energy providers one of the main focus of research has been on the improvement of ion transport. In lithium battery research this has led to the incorporation of various lithium salts, ceramics and plasticizers into the poly(ethylene)oxide (PEO) matrix, the polymer most used In Proton Conduction Membrane (PCM) fuel cell research this has led to the development of new membranes, which are designed with to replicate Nafion's ((c)DuPont) proton transport but also improve upon its deficiency of transporting intact fuel molecules and its dependence upon the presence of solvating water molecules. To better understand the process of ion transport, NMR was used to investigate dynamic properties such as D (self-diffusion coefficient) and T1 (spin-lattice relaxation time) of various proton and lithium ion-conducting systems. Ionic conductivity and viscosity measurements were also performed. The systems studied includes aqueous superacid solutions (trifluoromethanesulfonic (TFSA), para-toluenesulfonic (PTSA) and bis(trifluoromethanesulfonyl)imide (TFSI)); nano-porous (NP-) PCM's incorporating various ceramics and 3M fuel/2M H2SO4 solutions; and P(EO)20LiBETI (LiN(SO 2CF2CF3)2 composite incorporating SiO 2 ceramic nano particles. The objective of the study of the superacid solutions was to determine the effect of concentration on the transport. It was found that beyond the ionic conductivity maximum, fluctuations in both D and T1 supports the existence of local ordering in the ionic network, caused by the reduced solvent dielectric coefficient and increasing viscosity. Of the three superacids TFSA was the most conductive and most affected by reduced solvent concentration. For the P(EO)20LiBETI composite the aim was to determine the effect of the ceramic on the ion transport of the composite in a solvent free environment. Results show that the ceramic causes only modest increase in the lithium transport below 90°C. The objective in the

Aqueous Angiography: Real-Time and Physiologic Aqueous Humor Outflow Imaging.

Directory of Open Access Journals (Sweden)

Sindhu Saraswathy

Full Text Available Trabecular meshwork (TM bypass surgeries attempt to enhance aqueous humor outflow (AHO to lower intraocular pressure (IOP. While TM bypass results are promising, inconsistent success is seen. One hypothesis for this variability rests upon segmental (non-360 degrees uniform AHO. We describe aqueous angiography as a real-time and physiologic AHO imaging technique in model eyes as a way to simulate live AHO imaging.Pig (n = 46 and human (n = 6 enucleated eyes were obtained, orientated based upon inferior oblique insertion, and pre-perfused with balanced salt solution via a Lewicky AC maintainer through a 1mm side-port. Fluorescein (2.5% was introduced intracamerally at 10 or 30 mm Hg. With an angiographer, infrared and fluorescent (486 nm images were acquired. Image processing allowed for collection of pixel information based on intensity or location for statistical analyses. Concurrent OCT was performed, and fixable fluorescent dextrans were introduced into the eye for histological analysis of angiographically active areas.Aqueous angiography yielded high quality images with segmental patterns (p<0.0001; Kruskal-Wallis test. No single quadrant was consistently identified as the primary quadrant of angiographic signal (p = 0.06-0.86; Kruskal-Wallis test. Regions of high proximal signal did not necessarily correlate with regions of high distal signal. Angiographically positive but not negative areas demonstrated intrascleral lumens on OCT images. Aqueous angiography with fluorescent dextrans led to their trapping in AHO pathways.Aqueous angiography is a real-time and physiologic AHO imaging technique in model eyes.

Synthesis in aqueous medium and organic praseodymium complexes with ligands derived from Schiff base quinolinic. Characterization and physicochemical study; Sintesis en medio acuoso y organico de complejos de praseodimio con ligantes derivados de base de Schiff quinolicos. Caracterizacion y estudio fisicoquimico

Energy Technology Data Exchange (ETDEWEB)

Garcia G, A.

2015-07-01

It was investigated the coordination ability of the quinolinic Schiff base organic tetradentate quinolinic ligand (Q Schiff-(OH){sub 2}) towards the trivalent praseodymium by UV/Vis spectrophotometric titration (St). By St, was studied the formed species between the Q Schiff-(OH){sub 2} ligand and the praseodymium nitrate salt in equimolar concentrations (5.86 x 10{sup -4} M: 5.22 x 10{sup -4} M) in methanol. The statistical analysis of the experimental results suggested three complexed species with 1Pr:3L, 1Pr:2L y 1Pr:1L stoichiometries. The predominant stoichiometries were the second and the latter. Based on these results and data from the scientific literature, the methodology for the syntheses of the complexes Q Schiff-(OH){sub 2}-Pr in aqueous-organic and organic media was established and a molar ratio M:L= 1:2 of praseodymium nitrate and the ligand was used. The new complexes were characterized by UV/Vis, Infrared, X-ray Photoelectron Spectroscopy (XP S), Diffuse Reflectance (Dr) and Thermogravimetric Analysis/Differential Scanning Calorimetry (TGA/DSC). Elemental analysis of C, N, O and Pr by XP S suggested 1Pr:2L:1Na (PrC{sub 32}H{sub 20}N{sub 4}O{sub 4}Na) stoichiometry of the complex synthesized by the aqueous-organic medium while for the complex synthesized by the organic medium it was 1Pr:3L (PrC{sub 48}H{sub 33}N{sub 6}O{sub 6}). In the first case, the praseodymium ion charge was neutralized by the anionic ligands whose remaining charge was compensated by the sodium ion. In the second case, the ion charge was neutralized by the ligands. The minimum formula was Pr(Q Schiff){sub 2}Na for the pure coordination compound from the aqueous-organic medium and the minimum formula Pr(Q Schiff){sub 3} for that from the organic medium. XP S also indicated that the oxidation state of praseodymium ion was maintained. Both complexes were stable in methanol, ethanol and acetonitrile at least for 5 days. The photophysical properties of the studied complexes were

Modeling the Impact of Deformation on Unstable Miscible Displacements in Porous Media

Science.gov (United States)

Santillán, D.; Cueto-Felgueroso, L.

2014-12-01

Coupled flow and geomechanics is a critical research challenge in engineering and the geosciences. The simultaneous flow of two or more fluids with different densities or viscosities through deformable media is ubiquitous in environmental, industrial, and biological processes, including the removal of non-aqueous phase liquids from underground water bodies, the geological storage of CO2, and current challenges in energy technologies, such as enhanced geothermal systems, unconventional hydrocarbon resources or enhanced oil recovery techniques. Using numerical simulation, we study the interplay between viscous-driven flow instabilities (viscous fingering) and rock mechanics, and elucidate the structure of the displacement patterns as a function of viscosity contrast, injection rate and rock mechanical properties. Finally, we discuss the role of medium deformation on transport and mixing processes in porous media.

Pengaruh Variasi Temperatur Hidrotermal Pada Sintesis Lithium Mangan Oksida (Limn2o4 Spinel Terhadap Efisiensi Adsorpsi Dan Desorpsi Ion Lithium Dari Lumpur Sidoarjo

Directory of Open Access Journals (Sweden)

Yusuf Kurniawan

2014-09-01

Full Text Available Perkembangan teknologi dalam bidang material menunjukkan perkembangan yang sangat pesat dalam beberapa tahun terakhir.Salah satu material yang sangat dibutuhkan dalam berbagai aplikasi adalah lithium. Lithium sendiri bisa didapatkan dari air laut brines dan geothermal fluid. Salah satunya adalah Lumpur Sidoarjo. Lithium Mangan Oksida Spinel digunakan sebagai material absorben karena murah, tidak beracun dan mudah didapatkan. Pada penelitian ini metode hidrotermal digunakan sebagai metode sintesis pada LiMn2O4 karena dapat dilakukan pada temperatur yang relatif rendah dan menghasilkan partikel yang lebih homogen. Metode hidrotermal dilakukan pada temperatur 160 oC, 180 oC dan 200 oC selama 24 jam. Pengujian XRD dilakukan untuk mengetahui struktur kristal. Pengujian SEM dilakukan untuk mengetahui morfologi material setelah proses hidrotermal. Pengujian BET dilakukan untuk mengetahui surface area. Setelah itu metode acid treatment dilakukan untuk proses adsorpsi dan desorpsi. Adsorpsi dilakukan dengan mencelupkan Lithium Mangan Oksida Spinel yang telah disintesis kedalam Lumpur Sidoarjo.Pengujian ICP dilakukan untuk mengetahui kandungan lithium yang terdapat pada Lumpur Sidoarjo sebelum dan sesudah adsorpsi untuk mengetahui jumlah lithium yang terserap.Pengujian desorpsi dilakukan dengan mencelupkan LiMn2O4 kedalam larutan HCL. Pada uji XRD menunjukkan bahwa LiMn2O4 berstruktur kristal cubic. Dari hasil uji SEM terlihat bahwa tidak banyak perbedaan morfologi pada ketiga variasi.Partikel cenderung membentuk aglomerasi. Pada hasil uji ICP menunjukkan bahwa LiMn2O4 dengan temperatur hidrotermal 160oC memiliki efisiensi adsorpsi paling tinggi dengan 6,775 ppm. Sementara untuk desorpsi yang paling tinggi adalah 200oC sebesar 0.081 ppm

Nucleophilic addition of amines to the activated ethylene bond in non-aqueous media

International Nuclear Information System (INIS)

Perepichka, Igor F.; Popov, Anatolii F.

1995-01-01

The kinetics of addition of a number of primary and secondary aliphatic amines to trans-(2-furyl) nitro ethylene (1) has been studied in solvents of various polarities (from acetonitrile, ε 37.5, to heptane, ε 1.89). It has been shown that the reaction is catalysed both by the amine reagent and by tertiary amines. On the basis of analyzing the observed kinetic regularities a stepwise reaction mechanism has been proposed which involves formation of zwitterionic intermediate (3) at the first equilibrium step (k 1 , K 1 ) which is then converted into the reaction product by means of proton transfer in parallel routes, the non-catalytic one (k 2 ) and that catalysed by the initial (K 3 ) or tertiary (K 4 ) amine. The observed high values of the deuterium isotope effects in the reaction (K H /K D ∼ 2.3 - 8.9) confirm that proton transfer occurs in the rate-limiting step of the reaction (primary kinetic isotope effect). The third order by amine kinetic route is observed in low polar media which is due to participation of amine dimers (R 2 NH HNR 2 ) in the reaction. The observed kinetic regularities are compared with those for the nucleophilic aromatic substitution reactions in low-polar media, and the conclusion has been made that the reaction route of the third order by amine proceeds as reversible nucleophilic attack by amine dimer and following base-catalysed transformation of the intermediate into the product. (author)

Volumetric, ultrasonic and viscometric studies of solute–solute and solute–solvent interactions of l-threonine in aqueous-sucrose solutions at different temperatures

International Nuclear Information System (INIS)

Nain, Anil Kumar; Pal, Renu; Neetu

2013-01-01

Highlights: • The study reports density, ultrasonic speed and viscosity data of l-threonine in aqueous-sucrose solutions. • The study elucidates interactions of l-threonine with sucrose in aqueous media. • Provides data to estimate physicochemical properties of proteins in these media. • Correlates physicochemical properties of l-threonine with its behaviour in aqueous-sucrose solutions. -- Abstract: Densities, ρ of solutions of l-threonine in aqueous-sucrose solvents 5%, 10%, 15%, and 20% of sucrose, w/w in water at T = (293.15, 298.15, 303.15, 308.15, 313.15, and 318.15) K; and ultrasonic speeds, u and viscosities, η of these solutions at 298.15, 303.15, 308.15, 313.15, and 318.15 K were measured at atmospheric pressure. From these experimental results, the apparent molar volume, V ϕ , limiting apparent molar volume, V ϕ ∘ and the slope, S v , apparent molar compressibility, K s,ϕ , limiting apparent molar compressibility, K s,ϕ ∘ and the slope, S k , transfer volume, V ϕ,tr ∘ , transfer compressibility, K s,ϕ,tr ∘ , limiting apparent molar expansivity, E ϕ ∘ , Hepler’s constant, (∂ 2 V ϕ ∘ /dT 2 ), Falkenhagen coefficient, A, Jones–Dole coefficient, B and hydration number, n H have been calculated. The results have been interpreted in terms of solute–solvent and solute–solute interactions in these systems. The Gibbs energies of activation of viscous flow per mole of solvent, Δμ 1 ∘number sign and per mole of solute, Δμ 2 ∘number sign were also calculated and discussed in terms of transition state theory. It has been observed that there exist strong solute–solvent interactions in these systems and these interactions increase with increase in sucrose concentration in solution

Influence of formulation and processing variables on properties of itraconazole nanoparticles made by advanced evaporative precipitation into aqueous solution.

Science.gov (United States)

Bosselmann, Stephanie; Nagao, Masao; Chow, Keat T; Williams, Robert O

2012-09-01

Nanoparticles, of the poorly water-soluble drug, itraconazole (ITZ), were produced by the Advanced Evaporative Precipitation into Aqueous Solution process (Advanced EPAS). This process combines emulsion templating and EPAS processing to provide improved control over the size distribution of precipitated particles. Specifically, oil-in-water emulsions containing the drug and suitable stabilizers are sprayed into a heated aqueous solution to induce precipitation of the drug in form of nanoparticles. The influence of processing parameters (temperature and volume of the heated aqueous solution; type of nozzle) and formulation aspects (stabilizer concentrations; total solid concentrations) on the size of suspended ITZ particles, as determined by laser diffraction, was investigated. Furthermore, freeze-dried ITZ nanoparticles were evaluated regarding their morphology, crystallinity, redispersibility, and dissolution behavior. Results indicate that a robust precipitation process was developed such that size distribution of dispersed nanoparticles was shown to be largely independent across the different processing and formulation parameters. Freeze-drying of colloidal dispersions resulted in micron-sized agglomerates composed of spherical, sub-300-nm particles characterized by reduced crystallinity and high ITZ potencies of up to 94% (w/w). The use of sucrose prevented particle agglomeration and resulted in powders that were readily reconstituted and reached high and sustained supersaturation levels upon dissolution in aqueous media.

Media Komunitas dan Media Literacy

Directory of Open Access Journals (Sweden)

Pawito .

2013-12-01

Full Text Available Abstract:This essay deals with community media in relation to media literacy. After a short discussion on a number of community media characters is made the essay goes further with somewhat detail theoretical presumptions of the roles of media community with respect primarily to the development as Amartya Sen mentioned about. The author suggests that community media may play some significant roles in the development including (a disseminating information (from varieties of perspective, (b facilitating public discussion, (c helping to reach solutions of problems, (d encouraging participations, and (e encouraging the development of media literacy. Regarding the last point the author remarks that media community may have a dual-roles i.e facilitating community’s member in media participation and facilitating community’s member in media education.

Selective hydrolysis of phosphate monoester by a supramolecular phosphatase formed by the self-assembly of a bis(Zn(2+)-cyclen) complex, cyanuric acid, and copper in an aqueous solution (cyclen = 1,4,7,10-tetraazacyclododecane).

Science.gov (United States)

Zulkefeli, Mohd; Suzuki, Asami; Shiro, Motoo; Hisamatsu, Yosuke; Kimura, Eiichi; Aoki, Shin

2011-10-17

In Nature, organized nanoscale structures such as proteins and enzymes are formed in aqueous media via intermolecular interactions between multicomponents. Supramolecular and self-assembling strategies provide versatile methods for the construction of artificial chemical architectures for controlling reaction rates and the specificities of chemical reactions, but most are designed in hydrophobic environments. The preparation of artificial catalysts that have potential in aqueous media mimicking natural enzymes such as hydrolases remains a great challenge in the fields of supramolecular chemistry. Herein, we describe that a dimeric Zn(2+) complex having a 2,2'-bipyridyl linker, cyanuric acid, and a Cu(2+) ion automatically assembles in an aqueous solution to form a 4:4:4 complex, which is stabilized by metal-ligand coordination bonds, π-π-stacking interactions, and hydrogen bonding and contains μ-Cu(2)(OH)(2) cores analogous to the catalytic centers of phosphatase, a dinuclear metalloenzyme. The 4:4:4 complex selectively accelerates the hydrolysis of a phosphate monoester, mono(4-nitrophenyl)phosphate, at neutral pH.

From Augmentation Media to Meme Media.

Science.gov (United States)

Tanaka, Yuzuru

Computers as meta media are now evolving from augmentation media vehicles to meme media vehicles. While an augmentation media system provides a seamlessly integrated environment of various tools and documents, meme media system provides further functions to edit and distribute tools and documents. Documents and tools on meme media can easily…

Temperature-Invariant Aqueous Microgels as Hosts for Biomacromolecules.

Science.gov (United States)

Mastour Tehrani, Sepehr; Lu, Yijie; Guerin, Gerald; Soleimani, Mohsen; Pichugin, Dmitry; Winnik, Mitchell A

2015-10-12

Immobilization of enzymes on solid supports has been widely used to improve enzyme recycling, enzyme stability, and performance. We are interested in using aqueous microgels (colloidal hydrogels) as carriers for enzymes used in high-temperature reactions. These microgels should maintain their volume and colloidal stability in aqueous media up to 100 °C to serve as thermo-stable supports for enzymes. For this purpose, we prepared poly(N-hydroxyethyl acrylamide) (PHEAA) microgels via a two-step synthesis. First, we used precipitation polymerization in water to synthesize colloidal poly(diethylene glycol-ethyl ether acrylate) (PDEGAC) particles as a precursor. PDEGAC forms solvent swollen microgels in organic solvents such as methanol and dioxane and in water at temperatures below 15 °C. In the second step, these PDEGAC particles were transformed to PHEAA microgels through aminolysis in dioxane with ethanolamine and a small amount of ethylenediamine. Dynamic laser scattering studies confirmed that the colloidal stability of microgels was maintained during the aminolysis in dioxane and subsequent transfer to water. Characterization of the PHEAA microgels indicated about 9 mol % of primary amino groups. These provide functionality for bioconjugation. As proof-of-concept experiments, we attached the enzyme horseradish peroxidase (HRP) to these aqueous microgels through (i) N-(3-(dimethylamino)propyl)-N'-ethylcarbodiimide hydrochloride (EDC) coupling to the carboxylated microgels or (ii) bis-aryl hydrazone (BAH) coupling to microgels functionalized with 6-hydrazinonicotinate acetone (PHEAA-HyNic). Our results showed that HRP maintained its catalytic activity after covalent attachment (87% for EDC coupling, 96% for BAH coupling). The microgel enhanced the stability of the enzyme to thermal denaturation. For example, the residual activity of the microgel-supported enzyme was 76% after 330 min of annealing at 50 °C, compared to only 20% for the free enzyme under these

Pengaruh Temperatur Hydrothermal Terhadap Performa Elektrokimia Lifepo4 Sebagai Katoda Baterai Ion Lithium Type Aqueous Elektrolit

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Hendro Waluyo

2014-09-01

Full Text Available Katoda yang biasa digunakan produsen baterai lithium saat ini adalah LiCoO2. Dimana LiCoO2 memilki beberapa kekurangan beracun, tidak stabil, dan harganya mahal. Bahan katoda yang sangat menjanjikan adalah lithium iron phosphate (LiFePO4 untuk bisa menggantikan LiCoO2 .Dalam proses sintesis katoda LiFePO4 pada penelitian ini menggunakan metode hydrothermal dengan variasi temperatur 1500C,1750C dan 2000C selama 12 jam untuk waktu holdingnya. Dari hasil pengujian XRD menunjukkan terbentuknya fase LiFePO4 pada semua sampel, namun masih ditemukan zat pengotor. Untuk hasil uji SEM, serbuk LiFePO4 memiliki bentuk bulat tidak beraturan dan terjadi aglomerasi. Serbuk LiFePO4 dengan variasi temperatur 2000C memiliki performance yang paling baik dengan nilai kapasitas sebesar 109.32 mA/g hal ini karena dari hasil CV menunjukkan kinetik tranfer ion Lithium yang baik akibat distribusi ukuran partikel yang merata dan juga tingkat kristanilitas yang tinggi.

Social media management and media environment

Directory of Open Access Journals (Sweden)

Šiđanin Iva

2012-01-01

Full Text Available The paper deals with the system of services that social media management can offer to a variety of users. As social media systems are emerging, social media management can strengthen teams in social media and help to manage numerous social channels and distribution of social information from one place. Social media management is a system of procedures that are used to manage the flow of information in the environment of social media. This involves connecting with social media like Facebook, Twitter, LinkedIn, Plaxo, Ecademy, YouTube and many others, then the aggregation and management of social data. Social media management services are analysed through various fields, such as managing multiple social media profiles, mail scheduling and filtering, reporting and analytics. Social media management enables managing personal business through social media, which contributes to a significant reduction in expenditures. The paper also discusses the importance of social media management in marketing activities and various forms of social promotion, which allow companies to easily reach their customers.

Dissolution of anodic zirconium dioxide films in aqueous media

International Nuclear Information System (INIS)

Merati, A.; Cox, B.

1999-01-01

Zirconium with a low thermal neutron cross section, good corrosion resistance in high-temperature water, and high thermal conductivity is an ideal material for nuclear reactors. Its good resistance to water and steam at reactor temperatures is of the greatest interest to nuclear fuel designers. Dissolution of zirconium dioxide (ZrO 2 ) films in aggressive media was investigated. The extent of uniform and localized dissolution was measured by ultraviolet-visible (UV-VIS) spectrometry and an alternating current (AC) impedance test, respectively. Scanning electron microscopy (SEM) showed the extent of dissolution of ZrO 2 was a function only of the fluoride ion content and pH of the medium. Cathodic polarization was used to identify the preferred sites for localized dissolution of the oxide film. In 0.1 M potassium bifluoride (KHF 2 ), both uniform thinning and local breakdown of the oxide were observed. Within the limits of the investigating techniques, no evidence of dissolution was observed in the other solutions tested: 0.5 M sulfuric acid (H 2 SO 4 ). 1.0 M nitric acid (HNO 3 ), 5 M hydrochloric acid (HCl), or 0.1 M potassium fluoride (KF). In areas around iron-containing particles, fine cracks in the anodic oxide at prior metal grain boundaries and arrays of cracks in the oxide associated with residual scratches from the initial specimen preparation were the preferred spots for localized dissolution of the oxide film. Iron precipitates immediately below the surface of the oxide layer increased the local electrical conductivity. Enrichment of iron in the oxide matrix around these precipitates during the anodization process appeared to cause prospective spots, acting as anodic sites for pH formation

Kinetics and mechanism of the oxidation of uranium (IV) by hypochlorous acid in aqueous acidic perchlorate media

International Nuclear Information System (INIS)

Silverman, R.A.; Gordon, G.

1976-01-01

The oxidation of uranium(IV) by hypochlorous acid has been studied in aqueous sodium perchlorate--perchloric acid solutions. The reaction U 4 + + 2HOCl = UO 2 2 + + Cl 2 (aq) + 2H + proceeds appropriate to the rate law --d[U(IV)]/dt = k 0 . [U 4+ ][HOCl][H + ] -1 . At 25 0 and 3 M ionic strength, k 0 is 1.08 +- 0.07 sec -1 . Over the 1--25 0 temperature range, ΔH 2+ is 18.4 +- 0.1 kcal mole -1 , and ΔS 2+ is 3.1 +- 0.4 eu. The inverse hydrogen ion dependence of the rate law is explained by a rapid preequilibrium, in which a proton is lost from one of the reactants. A uranyl-like activated complex, [H 2 UO 2 Cl 3+ ] 2+ , is suggested, with one proton likely to be residing on each oxygen atom. Evidence is presented that the mechanism involves a two-electron transfer, with the intermediate chloride ion rapidly reacting with hypochlorous acid to form chlorine. The uranium(IV)-hypochlorous acid reaction plays an important role in the oxidation of uranium(IV) by aqueous chlorine solutions. The magnitude of this role was seriously underestimated by previous investigators

Safety in online media – freedom of the media; safety of media actors and media education

OpenAIRE

Moeller, Ch

2013-01-01

In this paper, prepared for the international conference ‘Mass Media – Society – Education: Media Safety Problems’ at the Chelyabinsk State University’s Department for Journalism and Media Education from September 30 – October 3, 2013, I would like to address three dimensions of media safety and security in online media.

Progress in aqueous rechargeable batteries

Directory of Open Access Journals (Sweden)

Jilei Liu

2018-01-01

Full Text Available Over the past decades, a series of aqueous rechargeable batteries (ARBs were explored, investigated and demonstrated. Among them, aqueous rechargeable alkali-metal ion (Li+, Na+, K+ batteries, aqueous rechargeable-metal ion (Zn2+, Mg2+, Ca2+, Al3+ batteries and aqueous rechargeable hybrid batteries are standing out due to peculiar properties. In this review, we focus on the fundamental basics of these batteries, and discuss the scientific and/or technological achievements and challenges. By critically reviewing state-of-the-art technologies and the most promising results so far, we aim to analyze the benefits of ARBs and the critical issues to be addressed, and to promote better development of ARBs.

Ion Movement in Polypyrrole/Dodecylbenzenesulphonate Films in aqueous and non-aqueous electrolytes

DEFF Research Database (Denmark)

Vidanapathirana, K.; Careem, M.A.; Skaarup, Steen

2002-01-01

The electrochemical characteristics during the redox process of polypyrrole (PPy) films, prepared using dodecylbenzenesulphonate (DBS-) dopant species, have been investigated using a combination of cyclic voltammetry and Electrochemical Quartz Crystal Microbalance (EQCM) measurements. Investigati......The electrochemical characteristics during the redox process of polypyrrole (PPy) films, prepared using dodecylbenzenesulphonate (DBS-) dopant species, have been investigated using a combination of cyclic voltammetry and Electrochemical Quartz Crystal Microbalance (EQCM) measurements....... Investigations were carried out using aqueous and non-aqueous electrolytes to study the effect of solvent on the ion movement during redox processes. When PPy films are cycled in aqueous electrolytes transport of both anion and cation occurs during oxidation and reduction. However, when cycled in the nonaqueous...

Comparative evaluation of aqueous humor viscosity.

Science.gov (United States)

Davis, Kyshia; Carter, Renee; Tully, Thomas; Negulescu, Ioan; Storey, Eric

2015-01-01

To evaluate aqueous humor viscosity in the raptor, dog, cat, and horse, with a primary focus on the barred owl (Strix varia). Twenty-six raptors, ten dogs, three cats, and one horse. Animals were euthanized for reasons unrelated to this study. Immediately, after horizontal and vertical corneal dimensions were measured, and anterior chamber paracentesis was performed to quantify anterior chamber volume and obtain aqueous humor samples for viscosity analysis. Dynamic aqueous humor viscosity was measured using a dynamic shear rheometer (AR 1000 TA Instruments, New Castle, DE, USA) at 20 °C. Statistical analysis included descriptive statistics, unpaired t-tests, and Tukey's test to evaluate the mean ± standard deviation for corneal diameter, anterior chamber volume, and aqueous humor viscosity amongst groups and calculation of Spearman's coefficient for correlation analyses. The mean aqueous humor viscosity in the barred owl was 14.1 centipoise (cP) ± 9, cat 4.4 cP ± 0.2, and dog 2.9 cP ± 1.3. The aqueous humor viscosity for the horse was 1 cP. Of the animals evaluated in this study, the raptor aqueous humor was the most viscous. The aqueous humor of the barred owl is significantly more viscous than the dog (P humor viscosity of the raptor, dog, cat, and horse can be successfully determined using a dynamic shear rheometer. © 2014 American College of Veterinary Ophthalmologists.

Decomposition of aqueous fluorene by γ-rays and product analysis

International Nuclear Information System (INIS)

Popov, P.; Getoff, Nikola

2004-01-01

Fluorene degradation was investigated in aqueous solution, saturated with air or N 2 O as a function of the absorbed radiation dose. The observed initial degradation yields (Gi values) are 2.41 and 1.04, respectively. In addition to these series, also studies were performed in media containing: 90% air and 10% N 2 O (Gi=1.1), 50% air and 50% N 2 O (Gi=0.9) and 10% air and 90% N 2 O (Gi=0.5). In all cases, as major degradation products 9-fluorenone and 9-fluorene carboxylic acid were found in addition to a mixture of aldehydes and carboxylic acids. Their yield depends on the starting pollutant concentration, absorbed radiation dose and oxygen content in the solution. For explanation of the results, probable reaction mechanisms are given

Chemical treatment of coal by grinding and aqueous caustic leaching

Energy Technology Data Exchange (ETDEWEB)

Balaz, P.; LaCount, R.B.; Kern, D.G.; Turcaniova, L. [Slovak Academy of Sciences, Kosice (Slovakia). Inst. of Geotechnics

2001-04-01

The aim of this work has been to point out the possibility of using GACL process for chemical cleaning of brown coal Nivaky (Slovakia) and Pittsburgh coal. Simultaneous grinding and aqueous chemical leaching, which is the principle of the process, reduces the inorganic and inorganic sulfur content in both coals. Dearsenificiation nearly up to 96% is detected in GACL-treated samples of Novaky coal. The possibility of enhancing the recovery of humic acid as a consequence of GACL treatment is demonstrated. The process under study works under atmospheric pressure, temperature of 90{degree}C and NaOH consumption, which is six times lower compared with the MCL process. Further research is needed to minimize the wear of grinding media and to improve the washing step. 24 refs., 7 figs., 3 tabs.

Synthesis of nc-UO{sub 2} by controlled precipitation in aqueous phase

Energy Technology Data Exchange (ETDEWEB)

Jovani-Abril, R., E-mail: raqueljovaniabril@gmail.com [European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O.Box 2340, D-76125 Karlsruhe (Germany); Gibilaro, M. [Laboratoire de Génie Chimique (LGC), Université de Toulouse, UMR CNRS 5503, 31062 Toulouse cedex 9 (France); Janßen, A.; Eloirdi, R.; Somers, J.; Spino, J.; Malmbeck, R. [European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O.Box 2340, D-76125 Karlsruhe (Germany)

2016-08-15

Nanocrystalline UO{sub 2} has been produced through controlled precipitation from an electrolytically reduced U(IV) solution. The reduction process of U(VI) to U(IV) was investigated by cyclic voltammetry in combination with absorption spectrophotometry. Precipitation was achieved by controlled alkalinisation following closely the solubility line of U(IV) in aqueous media. The highest starting concentration used was 0.5 M uranylnitrate which yielded, with the equipment used, around 10 g material pro batch. The produced nc-UO{sub 2} was characterised by transmission electron microscopy (TEM) and x-ray diffraction (XRD) and exhibited the typical UO{sub 2+x} fcc fluorite structure with an average crystallite size of 3.9 nm.

Adsorption of methyl orange from aqueous solution using chitosan/diatomite composite.

Science.gov (United States)

Zhao, Peng; Zhang, Runhu; Wang, Jianglin

2017-04-01

A novel chitosan/diatomite composite was prepared by a simple mixture in the mass ratio to remove methyl orange (MO) from aqueous media in this study. The composite adsorbent was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy analysis. The parameters to influence the adsorption of MO were studied under such conditions as kinetics, adsorption isotherm, pH effect, and thermodynamics. The results revealed that adsorption of MO was initially rapid and the equilibrium time was reached after 40 min. The optimal value of the pH was 5.0 for better adsorption. The equilibrium data were well fitted to the Langmuir isotherm compared to the Freundlich isotherm, and exhibited the highest capacity and a removal rate of 88.37% under an initial dye concentration of 50 mg/L. The kinetic data were well described by the pseudo-second order model. The thermodynamic calculations revealed that the sorption was viable, spontaneous, and exothermic under the conditions studied. In addition, the chitosan/diatomite composite had good adsorption and desorption performance with respect to reusability after six cycles. These results showed that the chitosan/diatomite could be considered as a potential adsorbent for the removal of MO in aqueous solution.

Investigation on the self-association of an inorganic coordination compound with biological activity (Casiope?na III-ia) in aqueous solution

OpenAIRE

Mar?n-Medina, Alejandro; Garc?a-Ramos, Juan Carlos; Ru?z-Azuara, Lena; Carrillo-Nava, Ernesto

2016-01-01

From studies using different experimental techniques employed to determine the presence of aggregates e.g. isothermal titration calorimetry, surface tension, electrical conductivity, UV?Vis spectrophotometry, dynamic and static light scattering, it is clearly demonstrated that the compound [Cu(4, 4?-dimethyl-2, 2?-bipyridine)(acetylacetonato)H2O]NO3 (Casiope?na III-ia), promising member of a family of new generation compounds for cancer treatment, is able to auto associate in aqueous media. P...

Media Literacy in Times of Media Divides

Directory of Open Access Journals (Sweden)

Kaja Žuran

2013-12-01

Full Text Available We live in a post-modern society, an information society, a society based around knowledge and participation, and above all in a media society. In a media culture where media holds a dominant position, we cannot overlook the emerging idea of a ‘media divide’ within the frame of media education, media literate individuals and the expansion of the traditional concept of media literacy. Firstly, we are in an era of technological revolution, and it is time to consider the meaning and function of media and how we experience it in our everyday life. Secondly, as a society we are subject to intense media invasion and we all need to learn how to use it to our benefit and apply a critical and autonomous perspective towards selecting media content. Otherwise the media divide between the media literate and illiterate will widen; but is there even a chance to overcome the supposed divide between those who are formally media educated and those who are not?

Study of radium extraction mechanisms from scales by leaching in different acidic and alkaline media

International Nuclear Information System (INIS)

Al-Masri, M. S.; Gafar, M.; Al-Kurdi, H.

2002-07-01

The present report shows the results of leaching experiments for scales containing naturally occuring radioactive materials using different acidic and alkaline media. The obtained result can be used for defining the method of safe disposal of such waste. Leaching solutions used in this study were distilled water, mineral acids (sulpharic acid, hydrochloric acid and nitric acid), sodium, potassium hydroxides, ammonium oxalate EDTA, sodium carbonate, potassium acetate, and a mixture of potassium chloride and hydrochloric acid. The results have shown that the extraction ratio of radium-226, the most abundant isotope in scales, is very low and even negligible using all different media. This indicates that all scales produced in Syrian oil fields do not require any chemical preparation before disposal. In addition, the effect of both stirring time of phrases and concentration of leaching media that may affect the radium transfer process from solid phase to aqueous phase have been investigated were no measurable amount being observed in the leachate. (author)

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

Development of Cellulose Acetate Microcapsules with Cyanex 923 for Phenol Removal from Aqueous Media

Directory of Open Access Journals (Sweden)

Irma Pérez-Silva

2018-01-01

Full Text Available Microcapsules of cellulose acetate with Cyanex 923 were prepared and used in this study for phenol removal from water and synthetic textile wastewater. The influence of several factors on the microcapsules extraction efficiency was studied, as well as characterization and phenol adsorption isotherm. Microcapsules characterization demonstrated the extractant reagent encapsulation, while in a batch mode procedure, good adsorption of phenol (ca. 5.5 × 10−3 mol Kg−1 has been reached. A slight decrease in phenol extraction percentage was obtained when synthetic textile wastewater was used (ca. 4.955 × 10−3 mol Kg−1, although a decrease in color was observed due to dye microcapsule extraction. Results indicate that this method is a promising alternative to conventional phenol removal technologies for aqueous samples of low phenol concentrations or in textile effluents.

Solid-phase extraction element based on epoxy polymer monolith for determination of polar organic compounds in aqueous media.

Science.gov (United States)

Takahashi, Tadashi; Odagiri, Kayo; Watanabe, Atsushi; Watanabe, Chuichi; Kubo, Takuya; Hosoya, Ken

2011-10-01

A solid-phase extraction element based on epoxy polymer monolith was fabricated for sorptive enrichment of polar compounds from liquid and gaseous samples. After ultrasonication of the element in an aqueous solution for a given period of time, the thermal desorption (TD) using a pyrolyzer with gas chromatography/mass spectrometry (GC/MS), in which TD temperature was programmed from 50 to 250 °C for the analytes absorbed in the element, was used to evaluate the element for basic extraction performance using the aqueous standard mixtures consisting of compounds having varied polarities such as hexanol, isoamyl acetate, linalool, furfural and decanoic acid, in concentrations ranging from 10 μg/L to 1 mg/L. Excellent linear relationships were observed for all compounds in the standard mixture, except decanoic acid. In the extraction of beverages such as red wine, the extraction element showed stronger adsorption characteristics for polar compounds such as alcohols and acids than a non-polar polydimethylsiloxane-based element. This feature is derived from the main polymer structure along with hydroxyl and amino groups present in the epoxy-based monolith polymer matrix. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

On the influence of hydronium and hydroxide ion diffusion on the hydrogen and oxygen evolution reactions in aqueous media

DEFF Research Database (Denmark)

Wiberg, Gustav Karl Henrik; Arenz, Matthias

2015-01-01

We present a study concerning the influence of the diffusion of H+ and OH- ions on the hydrogen and oxygen evolution reactions (HER and OER) in aqueous electrolyte solutions. Using a rotating disk electrode (RDE), it is shown that at certain conditions the observed current, i.e., the reaction rate...

Synthesis of assembled ZnO structures by precipitation method in aqueous media

International Nuclear Information System (INIS)

Sepulveda-Guzman, S.; Reeja-Jayan, B.; Rosa, E. de la; Torres-Castro, A.; Gonzalez-Gonzalez, V.; Jose-Yacaman, M.

2009-01-01

In this work, arrays of submicron ZnO structures were successfully synthesized using a one-step aqueous precipitation method. Snowflake-like and flower-like morphologies were obtained by changing the reaction temperature. X-ray diffraction (XRD) patterns indicated that the ZnO arrays have a wurtzite crystal structure. A possible growth mechanism based on the analysis done by scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and high-angle annular dark field (HAADF) is proposed. Our findings suggest that the growth mechanism of the ZnO arrays is by self-aggregation, and that such an oriented aggregation is enhanced by increasing the reaction temperature. The results also revealed that the aggregation process introduces several structural defects such as differences in mass distribution and crystalline structure. In order to study the surface chemical composition the samples were also characterized by XPS. The results showed the presence of Zn(OH) 2 and absorbed carbon species on the ZnO surface. In addition, the photoluminescence characterization showed that on UV excitation (λ = 360 nm) all samples present the characteristic UV emission centered at 390 nm, and for the sample synthesized at 60 deg. C, a visible emission was also observed

Synthesis of assembled ZnO structures by precipitation method in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Sepulveda-Guzman, S. [Centro de Innovacion, Investigacion y Desarrollo en Ingenieria y Tecnologia, UANL Km. 10 de la nueva carretera al Aeropuerto Internacional de Monterrey, PIIT Monterrey, Apodaca NL (Mexico); Facultad de Ingenieria Mecanica y Electrica de la UANL, Ciudad Universitaria San Nicolas de los Garza, Nuevo Leon C.P. 66451 (Mexico)], E-mail: ssepulveda@mail.uanl.mx; Reeja-Jayan, B. [Texas Materials Institute, University of Texas at Austin, 1 University Station C0803 (United States); Rosa, E. de la [Centro de Investigaciones en Optica, A.C. Loma del Bosque 115 Col. Lomas del Campestre, Leon Gto. C.P. 37150 (Mexico); Torres-Castro, A.; Gonzalez-Gonzalez, V. [Centro de Innovacion, Investigacion y Desarrollo en Ingenieria y Tecnologia, UANL Km. 10 de la nueva carretera al Aeropuerto Internacional de Monterrey, PIIT Monterrey, Apodaca NL (Mexico); Facultad de Ingenieria Mecanica y Electrica de la UANL, Ciudad Universitaria San Nicolas de los Garza, Nuevo Leon C.P. 66451 (Mexico); Jose-Yacaman, M. [Physics and Astronomy Department, University of Texas at San Antonio, 1604 Campus San Antonio, TX 78249 (United States)

2009-05-15

In this work, arrays of submicron ZnO structures were successfully synthesized using a one-step aqueous precipitation method. Snowflake-like and flower-like morphologies were obtained by changing the reaction temperature. X-ray diffraction (XRD) patterns indicated that the ZnO arrays have a wurtzite crystal structure. A possible growth mechanism based on the analysis done by scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and high-angle annular dark field (HAADF) is proposed. Our findings suggest that the growth mechanism of the ZnO arrays is by self-aggregation, and that such an oriented aggregation is enhanced by increasing the reaction temperature. The results also revealed that the aggregation process introduces several structural defects such as differences in mass distribution and crystalline structure. In order to study the surface chemical composition the samples were also characterized by XPS. The results showed the presence of Zn(OH){sub 2} and absorbed carbon species on the ZnO surface. In addition, the photoluminescence characterization showed that on UV excitation ({lambda} = 360 nm) all samples present the characteristic UV emission centered at 390 nm, and for the sample synthesized at 60 deg. C, a visible emission was also observed.

Reversible, All-Aqueous Assembly of Hydrogen-Bonded Polymersomes

Science.gov (United States)

Wang, Yuhao; Sukhishvili, Svetlana

2015-03-01

We report on sub-micron-sized polymersomes formed through single-step, all-aqueous assembly of hydrogen-bonded amphiphilic polymers. The hollow morphology of these assemblies was revealed by transmission electron microscopy (TEM), cryogenic scanning electron microscopy (cryo-SEM) and confocal laser scanning microscopy (CLSM). Stable in acidic media, these polymersomes could be dissolved by exposure to basic pH values. Importantly, the diameter of assembled hollow structures could be controlled in a wide range from 30 nm to 1 μm by the molecular weight of hydrogen-bonding polymers. We will discuss key quantitative aspects of these assemblies, including kinetics of hollow structure formation, time evolution of polymersome size, and the role of polymer molecular weight on membrane thickness and bending rigidity. We believe that our approach demonstrates an efficient and versatile way to rationally design nanocontainers for drug delivery, catalysis and personal care applications. This work was supported by the Innovation & Entrepreneurship doctoral fellowship from Stevens Institute of Technology.

[Chronic otitis mediaChronic Otitis Media].

Science.gov (United States)

Kohles, N; Schulz, T; Eßer, D

2015-11-01

There are 2 different kinds of chronic otitis media: Otitis media chronica mesotympanalis and otitis media chronica epitympanalis (cholesteatoma). The incidence of chronic otitis media as reported in literature differs in a wide range. The incidence rates vary between 0.45 and 46%. Both, otitis media chronica mesotympanalis and cholesteatoma, lead to eardrum perforation due to lengthy and recurring inflammations. Furthermore, chronic otitis media is characterized by frequently recurring otorrhea and conductive hearing loss. Georg Thieme Verlag KG Stuttgart · New York.

In Situ Cleanable Alternative HEPA Filter Media

International Nuclear Information System (INIS)

Adamson, D. J.; Terry, M. T.

2002-01-01

The Westinghouse Savannah River Company, located at the Savannah River Site in Aiken, South Carolina, is currently testing two types of filter media for possible deployment as in situ regenerable/cleanable High Efficiency Particulate Air (HEPA) filters. The filters are being investigated to replace conventional, disposable, glass-fiber, HEPA filters that require frequent removal, replacement, and disposal. This is not only costly and subjects site personnel to radiation exposure, but adds to the ever-growing waste disposal problem. The types of filter media being tested, as part of a National Energy Technology Laboratory procurement, are sintered nickel metal and ceramic monolith membrane. These media were subjected to a hostile environment to simulate conditions that challenge the high-level waste tank ventilation systems. The environment promoted rapid filter plugging to maximize the number of filter loading/cleaning cycles that would occur in a specified period of time. The filters were challenged using nonradioactive simulated high-level waste materials and atmospheric dust; materials that cause filter pluggage in the field. The filters are cleaned in situ using an aqueous solution. The study found that both filter media were insensitive to high humidity or moisture conditions and were easily cleaned in situ. The filters regenerated to approximately clean filter status even after numerous plugging and in situ cleaning cycles. Air Techniques International is conducting particle retention testing on the filter media at the Oak Ridge Filter Test Facility. The filters are challenged using 0.3-mm di-octyl phthalate particles. Both the ceramic and sintered media have a particle retention efficiency > 99.97%. The sintered metal and ceramic filters not only can be cleaned in situ, but also hold great potential as a long life alternative to conventional HEPA filters. The Defense Nuclear Facility Safety Board Technical Report, ''HEPA Filters Used in the Department of

Influence of different media on micromorphology of radiation synthesized poly(acrylamide-sodium acrylate) hydrogels

International Nuclear Information System (INIS)

Shan Jun; Chen Jie; Liu Zhanjun

1998-01-01

Poly(acrylamide-sodium acrylate) hydrogels were synthesized by 60 Co-γ ray radiation polymerization in aqueous solutions. The micromorphology of hydrogel samples dehydrated in the different alcohol media such as methanol, ethyl alcohol, n-propyl alcohol, iso-propyl alcohol, and tert-butyl alcohol was observed by scanning electron microscope (SEM). The critical concentrations at volume phase transition of the hydrogels in the different alcohol medium-water solutions were obtained. The results indicate that the hydrogel samples dehydrated in methanol and in ethyl alcohol display bubble-film network structures, and those in n-propyl alcohol and in iso-propyl alcohol and in tert-butyl alcohol demonstrate the porous structures including the dense phase. The reason is discussed from the critical concentrations and solubility parameters of different alcohol media. (author)

Dissolution properties of co-amorphous drug-amino acid formulations in buffer and biorelevant media.

Science.gov (United States)

Heikkinen, A T; DeClerck, L; Löbmann, K; Grohganz, H; Rades, T; Laitinen, R

2015-07-01

Co-amorphous formulations, particularly binary drug-amino acid mixtures, have been shown to provide enhanced dissolution for poorly-soluble drugs and improved physical stability of the amorphous state. However, to date the dissolution properties (mainly intrinsic dissolution rate) of the co-amorphous formulations have been tested only in buffers and their supersaturation ability remain unexplored. Consequently, dissolution studies in simulated intestinal fluids need to be conducted in order to better evaluate the potential of these systems in increasing the oral bioavailability of biopharmaceutics classification system class II drugs. In this study, solubility and dissolution properties of the co-amorphous simvastatin-lysine, gibenclamide-serine, glibenclamide-threonine and glibenclamide-serine-threonine were studied in phosphate buffer pH 7.2 and biorelevant media (fasted and fed state simulated intestinal fluids (FaSSIF and FeSSIF, respectively)). The co-amorphous formulations were found to provide a long-lasting supersaturation and improve the dissolution of the drugs compared to the crystalline and amorphous drugs alone in buffer. Similar improvement, but in lesser extent, was observed in biorelevant media suggesting that a dissolution advantage observed in aqueous buffers may overestimate the advantage in vivo. However, the results show that, in addition to stability advantage shown earlier, co-amorphous drug-amino acid formulations provide dissolution advantage over crystalline drugs in both aqueous and biorelevant conditions.

Uranium (VI) transport in saturated heterogeneous media: Influence of kaolinite and humic acid.

Science.gov (United States)

Chen, Chong; Zhao, Kang; Shang, Jianying; Liu, Chongxuan; Wang, Jin; Yan, Zhifeng; Liu, Kesi; Wu, Wenliang

2018-05-07

Natural aquifers typically exhibit a variety of structural heterogeneities. However, the effect of mineral colloids and natural organic matter on the transport behavior of uranium (U) in saturated heterogeneous media are not totally understood. In this study, heterogeneous column experiments were conducted, and the constructed columns contained a fast-flow domain (FFD) and a slow-flow domain (SFD). The effect of kaolinite, humic acid (HA), and kaolinite/HA mixture on U(VI) retention and release in saturated heterogeneous media was examined. Media heterogeneity significantly influenced U fate and transport behavior in saturated subsurface environment. The presence of kaolinite, HA, and kaolinite/HA enhanced the mobility of U in heterogeneous media, and the mobility of U was the highest in the presence of kaolinite/HA and the lowest in the presence of kaolinite. In the presence of kaolinite, there was no difference in the amount of U released from the FFD and SFD. However, in the presence of HA and kaolinite/HA, a higher amount of U was released from the FFD. The findings in this study showed that medium structure and mineral colloids, as well as natural organic matter in the aqueous phase had significant effects on U transport and fate in subsurface environment. Copyright © 2018 Elsevier Ltd. All rights reserved.

Optimization, isotherm, kinetic and thermodynamic studies of Pb(II) ions adsorption onto N-maleated chitosan-immobilized TiO2 nanoparticles from aqueous media

Science.gov (United States)

Shaker, Medhat A.; Yakout, Amr A.

2016-02-01

Chitosan, CS was chemically engineered by maleic anhydride via simple protocol to produce N-maleated chitosan, MCS which immobilized on anatase TiO2 to synthesize novel eco-friendly nanosorbent (51 ± 3.8 nm), MCS@TiO2 for cost-effective and efficient removal of Pb(II) ions from aqueous media. The chemical structure, surface properties and morphology of MCS@TiO2 were recognized by FTIR, 1H NMR, XRD, TEM, DLS and zeta-potential techniques. The relations between %removal of Pb(II) and different analytical parameters such as solution acidity (pH), MCS@TiO2 dosage, time of contact and initial Pb(II) concentration were optimized using response surface methodology (RSM) and Box-Behnken design (BBD) statistical procedures. The fitting of the experimental data to four different isotherm models at optimized conditions was carried out by various statistical treatments including the correlation coefficient (r), coefficient of determination (r2) and non-linear Chi-square (χ2) test analyses which all confirm the suitability of Langmuir model to explain the adsorption isotherm data. Also, statistics predicted that the pseudo-second-order model is the optimum kinetic model among four applied kinetic models to closely describe the rate equation of the adsorption process. Thermodynamics viewed the adsorption as endothermic and feasible physical process. EDTA could release the sorbed Pb(II) ions from MCS@TiO2 with a recovery above 92% after three sorption-desorption cycles. The novel synthesized nanosorbent is evidenced to be an excellent solid phase extractor for Pb(II) ions from wastewaters.

Neutron studies of paramagnetic fullerenols’ assembly in aqueous solutions

Science.gov (United States)

Lebedev, V. T.; Szhogina, A. A.; Suyasova, M. V.

2018-03-01

Recent results on structural studies of aqueous solutions of water-soluble derivatives of endofullerenes encapsulating 4f- and 3d-elements have been presented. Neutron small angle scattering experiments allowed recognize subtle features of fullerenols assembly as dependent on chemical nature (atomic number) of interior atom, pH-factor and temperature of solutions. It was observed a fractal-type fullerenols’ ordering at the scale of correlation radii ∼ 10-20 nm when molecules with iron atoms are integrated into branched structures at low concentrations (C ≤ 1 % wt.) and organized into globular aggregates at higher amounts (C > 1 % wt.). On the other hand, for Lanthanides captured in carbon cages the supramolecular structures are mostly globular and have larger gyration radii ∼ 30 nm. They demonstrated a good stability in acidic (pH ∼ 3) and neutral (pH ∼ 7) media that is important for forthcoming medical applications.

Chemical effects associated to (n, γ) nuclear reactions in diluted aqueous solutions of liquid or frozen organic halogenides

International Nuclear Information System (INIS)

Bermudez Rodriguez, I.M.

1985-09-01

Chemical effects associated to nuclear transformation 37 Cl (n, γ) 38 Cl or 127 I (n, γ) 128 I in solid or liquid aqueous solutions of ethyl iodide, trichloro-ethylene, thyroxine or DDT irradiated in a nuclear reactor are studied. The retention of radiohalogen under its initial chemical shape decrease with solute concentration in liquid phase but is almost constant with solute dilution in the solid phase. Potential applications in neutron activation analysis evidencing halogenated molecules in irradiated media are discussed. 57 refs [fr

Fed-state gastric media and drug analysis techniques: Current status and points to consider.

Science.gov (United States)

Baxevanis, Fotios; Kuiper, Jesse; Fotaki, Nikoletta

2016-10-01

Gastric fed state conditions can have a significant effect on drug dissolution and absorption. In vitro dissolution tests with simple aqueous media cannot usually predict drugs' in vivo response, as several factors such as the meal content, the gastric emptying and possible interactions between food and drug formulations can affect drug's pharmacokinetics. Good understanding of the effect of the in vivo fed gastric conditions on the drug is essential for the development of biorelevant dissolution media simulating the gastric environment after the administration of the standard high fat meal proposed by the FDA and the EMA in bioavailability/bioequivalence (BA/BE) studies. The analysis of drugs in fed state media can be quite challenging as most analytical protocols currently employed are time consuming and labour intensive. In this review, an overview of the in vivo gastric conditions and the biorelevant media used for their in vitro simulation are described. Furthermore an analysis of the physicochemical properties of the drugs and the formulations related to food effect is given. In terms of drug analysis, the protocols currently used for the fed state media sample treatment and analysis and the analytical challenges and needs emerging for more efficient and time saving techniques for a broad spectrum of compounds are being discussed. Copyright © 2016 Elsevier B.V. All rights reserved.

Some problems on the aqueous corrosion of structural materials in nuclear engineering

International Nuclear Information System (INIS)

Coriou, H.; Grall, L.

1964-01-01

The purpose of this report is to give a comprehensive view of some aqueous corrosion studies which have been carried out with various materials for utilization either in nuclear reactors or in irradiated fuel treatment plants. The various subjects are listed below. Austenitic Fe-Ni-Cr alloys: the behaviour of austenitic Fe-Ni-Cr alloys in nitric medium and in the presence of hexavalent chromium; the stress corrosion of austenitic alloys in alkaline media at high temperatures; the stress corrosion of austenitic Fe-Ni-Cr alloys in 650 C steam. Ferritic steels: corrosion of low alloy steels in water at 25 and 360 C; zirconium alloys; the behaviour of ultrapure zirconium in water and steam at high temperature. (authors) [fr

SINTESIS DAN KARAKTERISASI BIODIESEL DARI MINYAK KEMIRI SUNAN (Reutealis trisperma DENGAN VARIASI KONSENTRASI KATALIS NAOH

Directory of Open Access Journals (Sweden)

Holilah -

2014-06-01

Full Text Available Sintesis biodiesel dari minyak Kemiri Sunan (Reutealis trisperma (RTO menggunakan NaOH sebagai katalis dengan variasi konsentrasi katalis yaitu 0,5; 1,0; 1,5 dan 2,0 wt% telah diteliti. Minyak kemiri sunan (Reutealis trisperma adalah bahan baku yang menarik untuk produksi biodiesel. Biodiesel disintesis dengan dua tahap reaksi yaitu esterifikasi menggunakan katalis H2SO4 dan transesterifikasi dengan menggunakan katalis NaOH. Dalam penelitian ini, diteliti pengaruh konsentrasi katalis terhadap produk biodisel serta dan karakteristiknya. Hasil penelitian menunjukkan bahwa yield biodiesel meningkat seiring dengan meningkatnya konsentrasi katalis dari 0,5-1,0 wt%, selanjutnya dengan meningkatnya konsentrasi katalis dari 1,5-2,0 wt% membuat yield menurun. Yield optimum dicapai pada 84,7%. FAME (fatty  acid  methyl  ester diperoleh dengan konsentrasi katalis 1 wt% pada kondisi reaksi 65°C, waktu reaksi 1 jam dan rasio metanol minyak 1:2 (wt/wt. Karakteristik biodiesel diamati dengan uji standart bahan bakar dan hasilnya dibandingkan dengan standart ASTM D6751-02. Karakteristik biodiesel yang disintesis dengan konsentrasi katalis NaOH 1% adalah angka asam (0,55 mg KOH/g, densitas (0,90 gr/cm3, viskositas pada 40°C (9,2 cSt, angka setana (54,5 dan residu karbon (0,24 wt%/wt. This research was investigated bio diesel synthesis of Reutealis trisperma oil (RTO by using NaOH as a catalist with variation of catalyst concentration as follow 0.5; 1.0; 1.5 and 2,0 wt% . Reutealis trisperma oil is an attractive raw material for  bio diesel production. It was produced by two steps of reactions, they are esterification by using H2SO4 catalyst and transesterification by using NaOH catalyst. This study examined the effect of catalyst concentration on the yield of biodiesel and their selected properties. The result showed, that the bio diesel yield  with catalyst concentration increasing from 0,5-1,0 wt%, increased, while increasing the concentration from 1

In vitro activity of total aqueous ethanol leaf extracts of Ricinus communis on Leishmania major promastigotes

International Nuclear Information System (INIS)

Okech, B.G.A.; Irungu, L.W.; Anjili, C.O.; Munyua, J.K.; Njagi, E.N.M.; Rukungu, G.

2006-01-01

The activity of aqueous and ethanol extracts of Ricinus communis was tested on Leishmania promastigotes in cell-free culture media. Serial dilutions of the extracts ranging from 500μg/ml, 250 μg/ml and 62.5μg/ml were prepared in triplicate using Schneiders Drosophila medium supplemented with 20% fetal bovine serum in the absence of antibiotics and the growth of approximately 1x 10 (power 6) parasites monitored every two days for a period of 8 days. Parasite density was estimated every two days using the Neuabeur counting chamber. At the end of the 8-day period cell morphology was observed and photographed. Significant growth inihibitory effect was observed on the promastigotes by the aqueous and ethanol extracts especially at high concentrations. However, there was an enhanced growth effect initially thereafter leading to to a rapid decline in promastigote cell population. Flagellar motility was also greatly affected at high concentration and it appeared that there was a linear relationship between flagellar motilities and the level of concentrations. Parasite morphology was affected severely. Most of the cultures observed appeared to have abnormal round morphology. Rosseting was also evident in the extract treated cultures. The aqueous leaf extract interfered with parasite morphology but this was dose dependent. The importance of R. communis plant as a potential source for chemotypes with antileishmanial activity is discussed. (author)

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

International Nuclear Information System (INIS)

Howett, S.; Joseph, J.; Noel, J.J.; Wren, J.C.

2010-01-01

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

A Greener, Efficient Approach to Michael Addition of Barbituric Acid to Nitroalkene in Aqueous Diethylamine Medium

Directory of Open Access Journals (Sweden)

Hany J. Al-Najjar

2014-01-01

Full Text Available An efficient method for the synthesis of a variety of pyrimidine derivatives 3a–t by reaction of barbituric acids 1a,b as Michael donor with nitroalkenes 2a–k as Michael acceptor using an aqueous medium and diethylamine is described. This 1,4-addition strategy offers several advantages, such as using an economic and environmentally benign reaction media, high yields, versatility, and shorter reaction times. The synthesized compounds were identified by 1H-NMR, 13C-NMR, CHN, IR, and MS. The structure of compound 3a was further confirmed by single crystal X-ray structure determination.

A coumarin-derived Cu2 +-fluorescent chemosensor and its direct application in aqueous media

Science.gov (United States)

Mergu, Naveen; Kim, Myeongjin; Son, Young-A.

2018-01-01

A novel coumarin-based receptor bearing a benzohydrazide (FCBH) was developed as a fluorescent chemosensor with high selectivity toward Cu2 +. The sensor was successfully applied to the monitoring of Cu2 + in aqueous solution. After the addition of Cu2 + to FCBH, the color of the solution changed from greenish-yellow to red, and the absorption band at 457 nm red-shifted to 517 nm. The fluorescent green color of FCBH disappeared and the fluorescence emission was completely quenched in the presence of Cu2 +. Upon the addition of Cu2 +, deprotonation of FCBH occurred, and a 1:1 metal-ligand complex formed. DFT theoretical investigation was carried out to understand the behavior of the sensing probe toward Cu2 +. Additionally, the quenched fluorescence of the FCBH-Cu2 + complex was restored upon the addition of CN- ions. The possible sensing mechanism of FCBH toward Cu2 + was derived from experimental and theoretical examinations.

Simultaneous Extraction and Depolymerization of Fucoidan from Sargassum muticum in Aqueous Media

Directory of Open Access Journals (Sweden)

Elena M. Balboa

2013-11-01

Full Text Available The biomass components of the invasive seaweed Sargassum muticum were fractionated to allow their separate valorization. S. muticum (Sm and the solid residue remaining after alginate extraction of this seaweed (AESm were processed with hot, compressed water (hydrothermal processing to assess the effects of temperature on fucoidan solubilization. Fucose-containing oligosaccharides were identified as reaction products. Operating under optimal conditions (170 °C, up to 62 and 85 wt% of the dry mass of Sm and AESm were solubilized, respectively. The reaction media were subjected to precipitation, nanofiltration and freeze-drying. The dried products contained 50% and 85% of the fucoidan present in Sm and AESm, respectively; together with other components such as phenolics and inorganic components. The saccharidic fraction, accounting for up to 35% of the dried extracts, contained fucose as the main sugar, and also galactose, xylose, glucose and mannose. The concentrates were characterized for antioxidant activity using the TEAC assay.

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

International Nuclear Information System (INIS)

Thakur, Neha; Kumar, Sanjukta A.; Wagh, D.N.; Das, Sadananda; Pandey, Ashok K.; Kumar, Sangita D.; Reddy, A.V.R.

2012-01-01

Highlights: ► Th complexed with poly (bis[2-(methacryloyloxy)-ethyl]phosphate) as tailored polymer membranes. ► Membranes offered high capacity and selectivity for fluoride in aqueous media. ► Quantitative uptake (80 ± 5%) of fluoride. ► Fast sorption kinetics. ► 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 ≈76% sorption) than the sheet sorbent. But, the fluoride loading capacity of sheet sorbent (4320 mg kg −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.

Electrochemical detection of commercial silver nanoparticles: identification, sizing and detection in environmental media

International Nuclear Information System (INIS)

Stuart, E J E; Tschulik, K; Compton, R G; Omanović, D; Cullen, J T; Jurkschat, K; Crossley, A

2013-01-01

The electrochemistry of silver nanoparticles contained in a consumer product has been studied. The redox properties of silver particles in a commercially available disinfectant cleaning spray were investigated via cyclic voltammetry before particle-impact voltammetry was used to detect single particles in both a typical aqueous electrolyte and authentic seawater media. We show that particle-impact voltammetry is a promising method for the detection of nanoparticles that have leached into the environment from consumer products, which is an important development for the determination of risks associated with the incorporation of nanotechnology into everyday products. (paper)

An improved synthesis of 1,3,5-triaryl-2-pyrazolines in acetic acid aqueous solution under ultrasound irradiation

Directory of Open Access Journals (Sweden)

Lin Zhi-Ping

2007-03-01

Full Text Available Abstract Background Pyrazoline derivatives have been found to possess a broad spectrum of biological activities. Among various pyrazoline derivatives, 2-pyrazolines seem to be the most frequently studied. A variety of methods have been reported for the preparation of this class of compound. However, in spite of their potential utility, some of the reported methods suffer from drawbacks such as long reaction times, cumbersome product isolation procedures and environmental concerns. Organic reactions in aqueous media have attracted increasing interest recently because of environmental issues and the understanding of biochemical processes. Ultrasound has increasingly been used in organic synthesis in the last three decades. A large number of organic reactions can be carried out in higher yields, shorter reaction time or milder conditions under ultrasound irradiation. Results Preparation of a series of 1,3,5-triaryl-2-pyrazolines through the reaction of chalcones and phenylhydrazine hydrochloride was carried out in 83–96% yield within 1.5–2 h in sodium acetate-acetic acid aqueous solution under ultrasound irradiation. Conclusion We have described a practical and convenient procedure for the synthesis of 1,3,5-triaryl-2-pyrazolines in sodium acetate-acetic acid aqueous solution at room temperature under ultrasound irradiation.

Managing Media: Segmenting Media Through Consumer Expectancies

Directory of Open Access Journals (Sweden)

Matt Eastin

2014-04-01

Full Text Available It has long been understood that consumers are motivated to media differently. However, given the lack of comparative model analysis, this assumption is without empirical validation, and thus, the orientation of segmentation from a media management perspective is without motivational grounds. Thus, evolving the literature on media consumption, the current study develops and compares models of media segmentation within the context of use. From this study, six models of media expectancies were constructed so that motivational differences between media (i.e., local and national newspapers, network and cable television, radio, and Internet could be observed. Utilizing higher order statistical analyses the data indicates differences across a model comparison approach for media motivations. Furthermore, these differences vary across numerous demographic factors. Results afford theoretical advancement within the literature of consumer media consumption as well as provide media planners’ insight into consumer choices.

Sorption studies of Sn(II) and Zr(IV) on pistachio shell from different aqueous media

International Nuclear Information System (INIS)

Abdel-Fattah, A.A.; EI-Khouly, S.H.

2007-01-01

Sorption of Sn(lI) and Zr(IV) on pistachio shell as a solid sorbent material of particle sizes (0.5-1 mm) has been investigated from HNO 3 , H CI, HBr, NaNO 3 , Na CI, KBr and KI aqueous solutions. Before use, this substance was subjected to characterization tools including surface area, thermogravimetric analysis, infrared spectroscopy and X-R diffraction. The effect of contact time, weight of the resin, acid and salt concentrations and equilibrium ph on K d values have been studied. Sorption of both elements was found to verify Freundlich adsorption isotherm. The effect of temperature on thc sorption processes have been investigated and the thermodynamic functions δG, δH and δS have been determined. Adsorption processes have been discussed in the light of the obtained results

Non-aqueous pigmented inkjet inks

NARCIS (Netherlands)

DEROOVER, GEERT; Bernaerts, Katrien; HOOGMARTENS, IVAN

2009-01-01

A non-aqueous inkjet ink comprises a benzimidazolone pigment and a polymeric dispersant according to Formula (I): wherein, T represents hydrogen or a polymerization terminating group; Z represents theA non-aqueous inkjet ink comprises a benzimidazolone pigment and a polymeric dispersant according to

Protein imprinting and recognition via forming nanofilms on microbeads surfaces in aqueous media

International Nuclear Information System (INIS)

Lu Yan; Yan Changling; Wang Xuejing; Wang Gongke

2009-01-01

In this paler, we present a technique of forming nanofilms of poly-3-aminophenylboronic acid (pAPBA) on the surfaces of polystyrene (PS) microbeads for proteins (papain and trypsin) in aqueous. Papain was chosen as a model to study the feasibility of the technique and trypsin as an extension. Obtained core-shell microbeads were characterized using scanning electron microscopy (SEM), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and BET methods. The results show that pAPBA formed nanofilms (60-100 nm in thickness) on the surfaces of PS microbeads. The specific surface area of the papain-imprinted beads was about 180 m 2 g -1 and its pore size was 31 nm. These imprinted microbeads exhibit high recognition specificity and fast mass transfer kinetics. The specificity of these imprinted beads mainly originates from the spatial effect of imprinted sites. Because the protein-imprinted sites were located at, or close to, the surface, the imprinted beads have good site accessibility toward the template molecules. The facility of the imprinting protocol and the high recognition properties of imprinted microbeads make the approach an attractive solution to problems in the field of biotechnology.

Effect of Porous Media and Fluid Properties on Dense Non-Aqueous Phase Liquid Migration and Dilution Mass Flux

National Research Council Canada - National Science Library

Totten, Christian T

2005-01-01

.... Media grain size and NAPL wettability were varied for relative comparisons. Fluid properties including density differential and interfacial tension between NAPL and water were varied for relative comparisons...

The synthesis of aqueous-dispersible anatase TiO2 nanoplatelets

International Nuclear Information System (INIS)

Shan Guobin; Demopoulos, George P

2010-01-01

Aqueous well-dispersed and phase-pure anatase TiO 2 truncated octahedron nanoplatelets (NPLs) were prepared via controlled hydrolysis of titanium tetrachloride (TiCl 4 ) in ethylene glycol at 240 deg. C. Two shapes, square and hexagon, were observed by microscopy, exactly corresponding to the truncated octahedron NPLs. Ethylene glycol was found to produce water in situ that reacts with TiCl 4 to produce TiO 2 and HCl-the latter promoting TiO 2 colloid peptization. TiO 2 truncated octahedron NPLs are formed under the stabilizing action of ethylene glycol thermolysis derivatives, such as aldehydes. Crystal growth of the TiO 2 NPLs was affected by the reaction temperature that determines the water production rate and HCl-assisted peptization. TGA and FT-IR results showed ∼1.2% ethylene glycol thermolysis derivatives are attached to the surface of the TiO 2 NPLs, which prevents their agglomeration, hence making them easily dispersible in aqueous media. HR-TEM and SAED results showed that the TiO 2 NPLs are well crystallized and that the SAED patterns of the single TiO 2 NPL changes with its size and shape. XRD patterns showed that the TiO 2 NPLs are phase-pure anatase and the percentage of the {101} plane in the TiO 2 NPLs to be only 18%-a structural feature that renders the TiO 2 NPLs with enhanced UV absorption and reactivity properties.

Fabrication of Surface Protein-Imprinted Nanoparticles Using a Metal Chelating Monomer via Aqueous Precipitation Polymerization.

Science.gov (United States)

Li, Wei; Sun, Yan; Yang, Chongchong; Yan, Xianming; Guo, Hao; Fu, Guoqi

2015-12-16

Molecular imprinting is a promising way for constructing artificial protein recognition materials, but it has been challenged by difficulties such as restricted biomacromolecule transfer in the cross-linked polymer networks, and reduced template-monomer interactions that are due to the required aqueous media. Herein, we propose a strategy for imprinting of histidine (His)-exposed proteins by combining previous approaches such as surface imprinting over nanostructures, utilization of metal coordination interactions, and adoption of aqueous precipitation polymerization capable of forming reversible physical crosslinks. With lysozyme as a model template bearing His residues, imprinted polymer nanoshells were grafted over vinyl-modified nanoparticles by aqueous precipitation copolymerization of a Cu(2+) chelating monomer with a temperature-responsive monomer carried out at 37 °C, above the volume phase-transition temperature (VPTT) of the final copolymer. The imprinted nanoshells showed significant temperature sensitivity and the template removal could be facilitated by swelling of the imprinted layers at 4 °C, below the VPTT. The resultant core-shell imprinted nanoparticles exhibited strikingly high rebinding selectivity against a variety of nontemplate proteins. An imprinting factor up to 22.7 was achieved, which is among the best values reported for protein imprinting, and a rather high specific binding capacity of 67.3 mg/g was obtained. Moreover, this approach was successfully extended to preliminary imprinting of hemoglobin, another protein with accessible His. Therefore, it may be a versatile method for fabrication of high-performance surface-imprinted nanoparticles toward His-exposed proteins.

A Clean, Mild, and Efficient Preparation of Aryl 14H-benzo[a,j]xanthene leuco-dye Derivatives Via Nanocatalytic MCM-41-SO3H Under Ultrasonic Irradiation in Aqueous Media.

Science.gov (United States)

Fathollahi, Mostafa; Rostamizadeh, Shahnaz; Amani, Ali M

2018-01-01

The present study has developed an efficient and eco-friendly protocol for the synthesis of aryl-14-H-dibenzo[a,j] xanthenes through a one-pot condensation reaction of 2-naphthol and arylaldehydes in aqueous media using the nanocatalytic MCM-41-SO3H under ultrasonic illumination. Using SEM and XRD analyses, MCM-41-SO3H nanoparticles were characterized. Therefore, for high magnification, taking the SEM image, the mesoporous surface of MCM-41-SO3H nanoparticles coated with gold for 2 minutes was characterized. Moreover, at a scan rate of 0.02° (2θ)/sec, XRD analysis from 1.5° (2θ) to 10.0° (2θ) was performed. For our considered sample, some well-ordered XRD patterns with one main peak as well as three minor peaks equal to those of MCM-41 materials were observed. The suggested route demonstrates very promising properties like higher yields, decrease in the time of reaction (5-10 min), mild and straightforward conditions, low level of toxicity, and inclusion of a cost-efficient and ecofriendly catalyst having considerable reusability. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Experimental study and thermodynamic modelling of methane clathrate hydrate dissociation conditions in silica gel porous media in the presence of methanol aqueous solution

International Nuclear Information System (INIS)

Hashemi, Hamed; Javanmardi, Jafar; Zarifi, Mojdeh; Eslamimanesh, Ali; Mohammadi, Amir H.

2012-01-01

Highlights: ► Phase equilibria of hydrates of methane in confined silica gel pores are reported. ► Dissociation data in the presences of methanol aqueous solution are also measured. ► A thermodynamic model is developed for prediction of the obtained data. ► Acceptable agreement is found between the obtained data and the predicted results. - Abstract: In this work, the phase equilibria of clathrate hydrates of methane in the presence of pure water and 0.035 mass fraction of methanol aqueous solution in confined silica gel pores with (10 and 15) nm mean diameters are measured and reported. A thermodynamic model is also developed for prediction of the obtained experimental hydrate dissociation data. The Valderrama–Patel–Teja (VPT-EoS) equation of state (EoS) accompanied with the non-density dependent (NDD) mixing rules coupled with a previously developed activity model are applied to evaluate the fugacity of the species present and the activity coefficient of water in methanol aqueous solution. Acceptable agreement between the reported data and the predicted results using the proposed model and an existing method reported in the literature demonstrates the reliability of the presented model.

Media relations after the introduction of social media

OpenAIRE

Mesila, Helin

2010-01-01

In the light of the popularity of social media on one hand, and the contradictive relationships between journalists and public relations practitioners on the other hand, the thesis studies media relations after the introduction of social media. The study focuses on media relations in Estonian public relations scenery. The research answers to the questions: - What are media relations today? - What are the functions of social media and media relations in organizational communication? ...

Metal separations using aqueous biphasic partitioning systems

International Nuclear Information System (INIS)

Chaiko, D.J.; Zaslavsky, B.; Rollins, A.N.; Vojta, Y.; Gartelmann, J.; Mego, W.

1996-01-01

Aqueous biphasic extraction (ABE) processes offer the potential for low-cost, highly selective separations. This countercurrent extraction technique involves selective partitioning of either dissolved solutes or ultrafine particulates between two immiscible aqueous phases. The extraction systems that the authors have studied are generated by combining an aqueous salt solution with an aqueous polymer solution. They have examined a wide range of applications for ABE, including the treatment of solid and liquid nuclear wastes, decontamination of soils, and processing of mineral ores. They have also conducted fundamental studies of solution microstructure using small angle neutron scattering (SANS). In this report they review the physicochemical fundamentals of aqueous biphase formation and discuss the development and scaleup of ABE processes for environmental remediation

Removal of common organic solvents from aqueous waste streams via supercritical C02 extraction: a potential green approach to sustainable waste management in the pharmaceutical industry.

Science.gov (United States)

Leazer, Johnnie L; Gant, Sean; Houck, Anthony; Leonard, William; Welch, Christopher J

2009-03-15

Supercritical CO2 extraction of aqueous streams is a convenient and effective method to remove commonly used solvents of varying polarities from aqueous waste streams. The resulting aqueous layers can potentially be sewered; whereas the organic layer can be recovered for potential reuse. Supercritical fluid extraction (SFE) is a technology that is increasingly being used in commercial processes (1). Supercritical fluids are well suited for extraction of a variety of media, including solids, natural products, and liquid products. Many supercritical fluids have low critical temperatures, allowing for extractions to be done at modestly low temperatures, thus avoiding any potential thermal decomposition of the solutes under study (2). Furthermore, the CO2 solvent strength is easily tuned by adjusting the density of the supercritical fluid (The density is proportional to the pressure of the extraction process). Since many supercritical fluids are gases at ambient temperature, the extract can be concentrated by simply venting the reaction mixture to a cyclone collection vessel, using appropriate safety protocols.

Application of Eh-pH diagram for room temperature precipitation of zinc stannate microcubes in an aqueous media

International Nuclear Information System (INIS)

Al-Hinai, Ashraf T.; Al-Hinai, Muna H.; Dutta, Joydeep

2014-01-01

Graphical abstract: - Highlights: • One pot aqueous synthesis of zinc stannate (ZnSnO 3 ) particles at low temperature. • Synthesis designed with the assistance of potential-pH diagram. • ZnSnO 3 estimated to be stable between pH 8 and 12 was used for synthesis of the particles. • ZnSnO 3 ·3H 2 O were formed during the precipitation of zinc stannate. - Abstract: Potential-pH diagram assisted-design for controlled precipitation is an attractive method to obtain engineered binary and ternary oxide particles. Aqueous synthesis conditions of zinc stannate (ZnSnO 3 ) particles at low temperature were formulated with the assistance of potential-pH diagram. The pH of a solution containing stoichiometric amounts of Zn 2+ and Sn 4+ was controlled for the precipitation in a one pot synthesis step at room temperature (25 °C). The effect of the concentration of the reactants on the particle size was studied by varying the concentration of the precursor (Zn 2+ + Sn 4+ ) solution. Scanning electron micrographs show that the particles are monodispersed micron sized cubes formed by the self-organization of nano-sized crystallites. The obtained microcubes characterized by X-ray Diffraction and thermo gravimetric analysis (TGA) show that the particles are in ZnSnO 3 ·3H 2 O form

Formation and stabilization of anionic metal complexes in concentrated aqueous quaternary ammonium salt solutions

International Nuclear Information System (INIS)

Aronson, F.L.; Hwang, L.L.Y.; Ronca, N.; Solomon, N.A.; Steigman, J.

1985-01-01

Anionic complexes of transition metals were stabilized in aqueous solutions containing high concentrations of various short-chain quaternary ammonium salts. Compounds with longer paraffin chains were effective in much less concentrated solution. Complex ions were detected spectrophotometrically. FeCl 4 - , which is usually formed in concentrated HCl, was the predominant Fe(III) complex in 30 m choline chloride containing only 0.12 M HCl. A yellow transitory Tc(VII) chloro-addition intermediate, formed in the reduction of TcO 4 - by concentrated HCl, was stabilized when the solution also contained 25 m choline chloride. Its spectrum, as well as the isolation of an already known Tc(VII) bipyridyl complex, is reported. Concentrated organic electrolytes also stabilized Tc(V) oxide halides against disproportionation and Tc(IV) hexahalides against hydrolysis. Halochromates of Cr(VI) were formed and stabilized in dilute acid containing quaternary ammonium salts. Their UV spectra showed the well-resolved vibronic fine structure associated with the symmetric chromium-to-oxygen charge-transfer band. It is known that these progressions are resolved in aprotic solvents, but not in aqueous acidic solution alone, and that the loss of fine structure in aqueous media is due to hydrogen bonding. The stabilization of anionic metal complexes and the resolution of vibronic structure in halochromates are probably consequences of water-structure-enforced ion paring. The present work suggests that the water molecules in immediate contact with the complex anions are more strongly hydrogen bonded to each other than to the complex. 21 references, 4 figures

The aqueous chemistry of oxides

CERN Document Server

Bunker, Bruce C

2016-01-01

The Aqueous Chemistry of Oxides is a comprehensive reference volume and special topics textbook that explores all of the major chemical reactions that take place between oxides and aqueous solutions. The book highlights the enormous impact that oxide-water reactions have in advanced technologies, materials science, geochemistry, and environmental science.

Influence of coal properties on mercury uptake from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Lakatos, J.; Brown, S.D.; Snape, C.E. [Miskolc University, Miskolc-Egyetemvaros (Hungary). Research Inst. of Applied Chemistry

1999-10-01

The uptake of mercury (II) from aqueous solution by a range of coals has been studied and the results have been compared to those for a number of other sorbents, including commercial active carbons and cation-exchange resins. At pH 5 in a buffer medium, the capacities for mercury removal of the low-rank coals and the oxidized bituminous coals investigated are comparable to those of the other sorbents tested. For the lignites investigated, a high content of organic sulfur does not markedly affect the capacity for mercury uptake in relatively neutral and low chloride media, owing to redox reactions being the most likely mechanism involved. However, in highly acidic solutions, the capacities for mercury uptake are considerably greater for the high-sulfur coals investigated than for their low-sulfur counterparts due to chelation being the major sorption process involved. 36 refs., 4 figs., 7 tabs.

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

International Nuclear Information System (INIS)

Hoda, Numan; Budama, Leyla; Çakır, Burçin Acar; Topel, Önder; Ozisik, Rahmi

2013-01-01

Graphical abstract: TEM image of Pt nanoparticles produced by reducing by NaBH 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

Sorption studies of Sn(II) and Zr(IV) on pistachio shell from different aqueous media

Energy Technology Data Exchange (ETDEWEB)

Abdel-Fattah, A A [Nuclear Chemistry Dept., Atomic Energy Authority, Cairo (Egypt); EI-Khouly, S H [Radioisotopes and Generators Dept., Radioisotopes Prod. Division, Hot Lahoratories Center, Atomic Energy Authority, Cairo (Egypt)

2007-07-01

Sorption of Sn(lI) and Zr(IV) on pistachio shell as a solid sorbent material of particle sizes (0.5-1 mm) has been investigated from HNO{sub 3}, H CI, HBr, NaNO{sub 3}, Na CI, KBr and KI aqueous solutions. Before use, this substance was subjected to characterization tools including surface area, thermogravimetric analysis, infrared spectroscopy and X-R diffraction. The effect of contact time, weight of the resin, acid and salt concentrations and equilibrium ph on K{sub d} values have been studied. Sorption of both elements was found to verify Freundlich adsorption isotherm. The effect of temperature on thc sorption processes have been investigated and the thermodynamic functions {delta}G, {delta}H and {delta}S have been determined. Adsorption processes have been discussed in the light of the obtained results.

SOCIAL MEDIA

Science.gov (United States)

RESPONSIBILITY CENTCOM COALITION MEDIA SOCIAL MEDIA NEWS ARTICLES PRESS RELEASES IMAGERY VIDEOS TRANSCRIPTS VISITORS AND PERSONNEL FAMILY CENTER FAMILY READINESS CENTCOM WEBMAIL SOCIAL MEDIA SECURITY ACCOUNTABILITY HomeMEDIASOCIAL MEDIA Social Media CENTCOM'S ENGLISH SOCIAL MEDIA ACCOUNTS There are many U.S. military commands

f-Element Ion Chelation in Highly Basic Media

International Nuclear Information System (INIS)

Paine, R.T.

2000-01-01

A large body of data has been collected over the last fifty years on the chemical behavior of f-element ions. The ions undergo rapid hydrolysis reactions in neutral or basic aqueous solutions that produce poorly understood oxide-hydroxide species; therefore, most of the fundamental f-element solution chemistry has allowed synthetic and separations chemists to rationally design advanced organic chelating ligands useful for highly selective partitioning and separation of f-element ions from complex acidic solution matrices. These ligands and new examples under development allow for the safe use and treatment of solutions containing highly radioactive species. This DOE/EMSP project was undertaken to address the following fundamental objectives: (1) study the chemical speciation of Sr and lanthanide (Ln) ions in basic aqueous media containing classical counter anions found in waste matrices; (2) prepare pyridine N-oxide phosphonates and phosphonic acids that might act as selective chelators for Ln ions in model basic pH waste streams; (3) study the binding of the new chelators toward Ln ions and (4) examine the utility of the chelators as decontamination and dissolution agents under basic solution conditions. The project has been successful in attacking selected aspects of the very difficult problems associated with basic pH solution f-element waste chemistry. In particular, the project has (1) shed additional light on the initial stages of Ln ion sol-gel-precipitate formulation under basic solution conditions; (2) generated new families of pyridine phosphonic acid chelators; (3) characterized the function of the chelators and (4) examined their utility as oxide-hydroxide dissolution agents. These findings have contributed significantly to an improved understanding of the behavior of Ln ions in basic media containing anions found in typical waste sludges as well as to the development of sludge dissolution agents. The new chelating reagents are easily made and could be

Recent results on aqueous electrolyte cells

KAUST Repository

Wessells, Colin; Huggins, Robert A.; Cui, Yi

2011-01-01

The improved safety of aqueous electrolytes makes aqueous lithium-ion batteries an attractive alternative to commercial cells utilizing flammable and expensive organic electrolytes. Two important issues relating to their use have been addressed

Generalized corrosion of nickel base alloys in high temperature aqueous media: a contribution to the comprehension of the mechanisms

International Nuclear Information System (INIS)

Marchetti-Sillans, L.

2007-11-01

In France, nickel base alloys, such as alloy 600 and alloy 690, are the materials constituting steam generators (SG) tubes of pressurized water reactors (PWR). The generalized corrosion resulting from the interaction between these alloys and the PWR primary media leads, on the one hand, to the formation of a thin protective oxide scale (∼ 10 nm), and on the other hand, to the release of cations in the primary circuit, which entails an increase of the global radioactivity of this circuit. The goal of this work is to supply some new comprehension elements about nickel base alloys corrosion phenomena in PWR primary media, taking up with underlining the effects of metallurgical and physico-chemical parameters on the nature and the growth mechanisms of the protective oxide scale. In this context, the passive film formed during the exposition of alloys 600, 690 and Ni-30Cr, in conditions simulating the PWR primary media, has been analyzed by a set of characterization techniques (SEM, TEM, PEC and MPEC, XPS). The coupling of these methods leads to a fine description, in terms of nature and structure, of the multilayered oxide forming during the exposition of nickel base alloys in primary media. Thus, the protective part of the oxide scale is composed of a continuous layer of iron and nickel mixed chromite, and Cr 2 O 3 nodules dispersed at the alloy / mixed chromite interface. The study of protective scale growth mechanisms by tracers and markers experiments reveals that the formation of the mixed chromite is the consequence of an anionic mechanism, resulting from short circuits like grain boundaries diffusion. Besides, the impact of alloy surface defects has also been studied, underlining a double effect of this parameter, which influences the short circuits diffusion density in oxide and the formation rate of Cr 2 O 3 nodules. The sum of these results leads to suggest a description of the nickel base alloys corrosion mechanisms in PWR primary media and to tackle some

Acoustic imaging of vapor bubbles through optically non-transparent media

International Nuclear Information System (INIS)

Kolbe, W.F.; Turko, B.T.; Leskovar, B.

1983-10-01

A preliminary investigation of the feasibility of acoustic imaging of vapor bubbles through optically nontransparent media is described. Measurements are reported showing the echo signals produced by air filled glass spheres of various sizes positioned in an aqueous medium as well as signals produced by actual vapor bubbles within a water filled steel pipe. In addition, the influence of the metallic wall thickness and material on the amplitude of the echo signals is investigated. Finally several examples are given of the imaging of spherical bubbles within metallic pipes using a simulated array of acoustic transducers mounted circumferentially around the pipe. The measurement procedures and a description of the measuring system are also given

CLASSICAL MEDIA RELATIONS AND NEW MEDIA RELATIONS IN SPORT

Directory of Open Access Journals (Sweden)

Alexandru Lucian MIHAI

2014-06-01

Full Text Available Media relations in sport mean maintenance of networks and positive relationships with people in the media to obtain positive media exposure for a sport product (informal and formal information sessions with media representatives. Because of the pervasive influence the media has on marketing success, sport marketers must make concerted efforts to create a positive relationship between their sport event and the media. They may accomplish this by providing the media with press releases, having news conferences, having media-day events (in which the media are invited to interact with the players, coaches, and administrators, providing media guides for the respective sport events and so on. Each of these activities promotes active involvement from the media, which will subsequently contribute to relationship building with the community.

A systems biology framework for pathway level culture media engineering: pplication to Pichia pastoris cultures

OpenAIRE

Ferreira, Ana Raquel Santos

2012-01-01

Dissertação para obtenção do Grau de Doutor em Engenharia Química e Bioquímica Culture media (CM) formulations contain hundreds of ingredients in aqueous solutions that may be involved in complex interactions in the same or competing pathways within the cell. This thesis proposes a new methodology for determining the optimal composition of CM that migrates from an empirical to a mechanistic or hybrid mechanistic CM development approach. A framework consisting in the execution of an a...

Media education and media influence on youth

OpenAIRE

LILÁK, Karel

2011-01-01

Bachelor´s work is focused on the questions of the medial education and the medias themselves. This work also investigate with the influence of the action of medias to the students of apprenticeship. The first part of the theoretical work has generally explains what is media education, what is its significance for society and for the benefit of education in school. They are given functions, types and objectives of media education and communications capabilities via the media. The second part ...

UKURAN PARTIKEL DAN KONFORMASI KRISTAL ZEOLIT-A HASIL SINTESIS DENGAN PENAMBAHAN TETRAPROPILAMMONIUM HIDROKSIDA (TPAOH

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Nurul - Widiastuti

2014-12-01

Full Text Available Abstract PARTICLE SIZE AND CRYSTAL CONFORMATION OF SYNTHESIZED ZEOLITE-A WITH TETRAPROPYLAMMONIUM HYDROXIDE (TPAOH ADDITION. The aims of this research is to study the effect of tetrapropylammonium hydroxide (TPAOH concentration in the synthesis of zeolite A to its physical characteristics such as crystallinity, crystal conformation and average crystal size. The zeolite A was synthesized with composition 3.165 Na2O : 1.000 Al2O3 : 1.926 SiO2 : 128 H2O : x TPAOH where x was 0; 0.0385; 0.0577; 0.0770; 0.1540 and 4.1602. The zeolite was crystalized under hydrothermal condition in a stainless steel autoclave at 100°C for 5 hours. The resulting crystal was washed with distilled water until pH 8 and then dried in an oven at 80oC for 24 hours. FT-IR and XRD analysis results show that the synthesized zeolite A at x = 4.1602 has the lowest crystallinity. It is estimated due to the mass of TPAOH was four times higger than the mass of zeolite framework components (Si and Al. SEM and PSD (Particle Size Distribution analysis results show that TPAOH concentration affected the crystal conformation and the average size of zeolite A particles. The formation of chained crystal conformation was caused by the electrostatic interactions between TPA+ and negatively charge of zeolite framework. In addition, the particel size of the synthesized zeolite A at x = 0.1540 was 2.024 µm which was smaller than the particel size of the synthesized zeolite A without TPAOH, which was 3.534 µm. Keywords: average size of particles; crystal conformation; TPAOH; zeolite A Abstrak Penelitian ini bertujuan untuk mempelajari pengaruh konsentrasi TPAOH (Tetrapropilamonium hidroksida dalam sintesis zeolit A terhadap sifat fisikanya yang meliputi kekristalan, konformasi kristal dan ukuran rata-rata kristal yang terbentuk. Pada penelitian   ini   zeolit A   disintesis    dengan komposisi 3,165 Na2O : 1 Al2O3 : 1,926 SiO2 :128 H2O: x TPAOH. Konsentrasi TPAOH divariasikan dengan

Changes to the Aqueous Humor Proteome during Glaucoma.

Science.gov (United States)

Kaeslin, Martha Andrea; Killer, Hanspeter Ezriel; Fuhrer, Cyril Adrian; Zeleny, Nauke; Huber, Andreas Robert; Neutzner, Albert

2016-01-01

To investigate the aqueous humor proteome in patients with glaucoma and a control group. Aqueous humor was obtained from five human donors diagnosed with primary open angle glaucoma (POAG) and five age- and sex-matched controls undergoing cataract surgery. Quantitative proteome analysis of the aqueous humor by hyper reaction monitoring mass spectrometry (HRM-MS) based on SWATH technology was performed. Expression levels of 87 proteins were found to be different between glaucomatous and control aqueous humor. Of the 87 proteins, 34 were significantly upregulated, whereas 53 proteins were downregulated in the aqueous humor from glaucoma patients compared to controls. Differentially expressed proteins were found to be involved in cholesterol-related, inflammatory, metabolic, antioxidant as well as proteolysis-related processes. Glaucoma leads to profound changes to the aqueous humor proteome consistent with an altered metabolic state, an inflammatory response and impaired antioxidant defense.

Removal of Parathion from Aqueous Media Through p-tert-Butylcalix[4]arene Based Modified Silica

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Sibghatullah Memon

2013-12-01

Full Text Available This study explores, adsorption efficiency of p-tert-butylcalix[4]arene based modified silica to remove parathion from aqueous environment. The adsorption parameters, i.e. pH, concentration of pesticide solution, contact time and adsorbent dosage were optimized, as 10, 1 mg L-1, 40 min and 0.04 g, respectively. Langmuir, Freundlich and Dubinin-Radushkevich (D-R isotherm models were used to evaluate the adsorption mechanism. Adsorption constants values of these models suggest that the adsorption of parathion is favorable and were found to be best fit with Freundlich isotherm. From the kinetic study it can be predicted that adsorption of parathion follows Ho and McKay model (pseudo-second order. Thermodynamic parameters, enthalpy (ΔH, entropy (ΔS and Gibbs free energy (ΔG have also been evaluated and were found as -132.25, 0.45, -4.14 Jmol-1, respectively.

The effect of thermal treatment on the fracture properties of alloy X-750 in aqueous environments

International Nuclear Information System (INIS)

Ballinger, R.; Elliott, C.S.; Hwang, I.S.; Prybylowski, J.

1993-05-01

Alloy X-750 is a high strength, age hardenable nickel-base alloy used in light water nuclear reactors. The excellent corrosion resistance and high temperature strength of alloy X-750 make it suitable for use in a variety of structure components in both pressurized water reactors and boiling water reactors. These applications involve exposure of highly stressed material to aqueous media. Operational stresses are subject to low frequency thermally induced fluctuations and high frequency flow induced fluctuations. In general, alloy X-750 has performed well in light water reactors. However, an economically significant number of components have failed unexpectedly due to localized forms of attack such as corrosion fatigue and stress corrosion cracking. Thermal processing history is known to play a significant role in the fracture properties of alloy X-750 in aqueous environments. While thermal treatments have been developed recently to improve performance, in many cases the reason for improved performance remains unclear. Therefore, identification of the mechanisms responsible for the degradation of fracture properties in aqueous environments is necessary. As a corollary it is necessary to achieve an understanding of how thermal treatment influences microstructure and, in turn, how microstructure influences fracture properties in aqueous environments. This report discusses five thermal treatments which were studied: (1) SA-1 hr at 1093 degree C, (2) AH - 24 hr at 885 degree C + 20 hr at 704 degree C, (3) HTH - 1 hr at 1093 degree C + 20 hr at 704 degree C, (4) AHTH - 1 hr at 1093 degree C + 24 hr at 885 degree C + 20 hr at 704 degree C, and (5) HOA - 1 hr at 1093 degree C + 100 hrs at 760 degree C. Microstructural characterization of these materials was accomplished through the use of optical microscopy, transmission electron microscopy,scanning transmission electron microscopy, energy dispersive x-ray spectroscopy, and x-ray diffractometry

Effect of {alpha}-Particle and X-Ray Irradiation on DNA Synthesis in Tissue Cultures; Effet de l'Irradiation par les Particules a et par les Rayons X sur la Synthese de l'ADN dans des Cultures de Tissus; 0412 043b 0438 044f 0414 ; Efectos de la Irradiacion con Particulas Alfa y con Rayos X sobre la Sintesis de ADN en Cultivos de Tejidos

Energy Technology Data Exchange (ETDEWEB)

Smith, C. L. [Department of Radiotherapeutics, University of Cambridge, Cambridge (United Kingdom)

1962-02-15

lesions subies par la structure type de l'ADN (ou du phosphate de l'ADN) pendant la phase exponentielle dela synthese, les observations formulees plus haut sous 1, 2 et 3 constituent les corollaires evidents de ce phenomene. (author) [Spanish] La memoria describe los efectos de las particulas {alpha} y de los rayos X sobre la velocidad de sintesis del ADN en cultivos de tejidos de fibroblastos y de celulas de HeLa del raton. Los autores emplearon el metodo de la microautorradiografia con timidina tritiada, que les permitio evaluar la velocidad de sintesis en los cultivos de una sola capa que utilizaron. Los resultados indican que: 1) La fraccion de celulas que sintetizan ADN en un cultivo no es alterada por las particulas a. ni por los rayos X en las dosis experimentales empleadas. 2) Ambos tipos de radiaciones reducen la velocidad de sintesis del ADN en las celulas irradiadas. 3) El efecto de una dosis determinada de cualquiera de las dos radiaciones es disminuir la velocidad de sintesis de todas las celulas hasta una fraccion constante de la velocidad correspondiente a las celulas no irradiadas. 4) En. el caso de los fibroblastos del raton, la velocidad de sintesis del ADN queda reducida en un 37 por ciento (1/e) por una dosis a del orden de 25 {alpha}/{mu}{sup 2} o por una dosis de rayos X de 14 000 rad( En el caso de las celulas de HeLa, se requiere una dosis de unos 90 000 rad para alcanzar el mismo efecto. 5) La disminucion de la velocidad de sintesis se produce menos de media hora despues de la irradiacion, por lo que podria tratarse de un efecto inmediato. El resultado 4) permite calcular aproximadamente la forma del blanco. Si seo supone que es cilindrico, enoel caso de los fibroblastos, tendria un diametro aproximado de 16 A y una longitud de 16 000 A, es decir, se trataria de un cilindro extremadamente alargado con un peso molecular del orden de 5 x 10{sup 7}. Para las celulas de HeLa se obtendria un peso molecular de 10{sup 7}. Los resultados concuerdan con la

Changes to the Aqueous Humor Proteome during Glaucoma.

Directory of Open Access Journals (Sweden)

Martha Andrea Kaeslin

Full Text Available To investigate the aqueous humor proteome in patients with glaucoma and a control group.Aqueous humor was obtained from five human donors diagnosed with primary open angle glaucoma (POAG and five age- and sex-matched controls undergoing cataract surgery. Quantitative proteome analysis of the aqueous humor by hyper reaction monitoring mass spectrometry (HRM-MS based on SWATH technology was performed.Expression levels of 87 proteins were found to be different between glaucomatous and control aqueous humor. Of the 87 proteins, 34 were significantly upregulated, whereas 53 proteins were downregulated in the aqueous humor from glaucoma patients compared to controls. Differentially expressed proteins were found to be involved in cholesterol-related, inflammatory, metabolic, antioxidant as well as proteolysis-related processes.Glaucoma leads to profound changes to the aqueous humor proteome consistent with an altered metabolic state, an inflammatory response and impaired antioxidant defense.

Poly (ethylene oxide)-block-poly (n-butyl acrylate)-blockpoly (acrylic acid) triblock terpolymers with highly asymmetric hydrophilic blocks: synthesis and aqueous solution properties

OpenAIRE

Petrov, P. (Petar); Yoncheva, K. (Krassimira); Mokreva, P. (Pavlina); Konstantinov, S. (Spiro); Irache, J.M. (Juan Manuel); Müller, A.H.E. (Axel H.E.)

2013-01-01

The synthesis and aggregation behaviour in aqueous media of novel amphiphilic poly(ethylene oxide)- block-poly(n-butyl acrylate)-block-poly(acrylic acid) (PEO–PnBA–PAA) triblock terpolymers were studied. Terpolymers composed of two highly asymmetric hydrophilic PEO (113 monomer units) and PAA (10–17 units) blocks, and a longer soft hydrophobic PnBA block (163 or 223 units) were synthesized by atom transfer radical polymerisation (ATRP) of n-butyl acrylate and tert-butyl acrylate ...

investigations on the use of surfactants for the separation of some organics and metal ions from aqueous media

International Nuclear Information System (INIS)

Mahmoud, M.R.

2007-01-01

the copreceipitate flotation of 137 Cs from dilute aqueous solutions and simulated radioactive wastes using nickel hexacyanoferrate(11) as a co precipitant and sodium lauryl sulfate, cetyltrimethylammonium bromide,or dodecyl amine as a collect or was extensively investigated to establish the best conditions for cesium removal. under the optimal conditions, removals exceeding 99% and decontamination factors higher than 110 could be achieved for the radioactive waste simulant. the results are compared with those obtained by conventional removal methods and are discussed in terms of the collector properties and the electrical state of the co precipitate

Enhancement of hybridoma formation, clonability and cell proliferation in a nanoparticle-doped aqueous environment

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Karnieli Ohad

2008-01-01

Full Text Available Abstract Background The isolation and production of human monoclonal antibodies is becoming an increasingly important pursuit as biopharmaceutical companies migrate their drug pipelines away from small organic molecules. As such, optimization of monoclonal antibody technologies is important, as this is becoming the new rate-limiting step for discovery and development of new pharmaceuticals. The major limitations of this system are the efficiency of isolating hybridoma clones, the process of stabilizing these clones and optimization of hybridoma cell secretion, especially for large-scale production. Many previous studies have demonstrated how perturbations in the aqueous environment can impact upon cell biology. In particular, radio frequency (RF irradiation of solutions can have dramatic effects on behavior of solutions, cells and in particular membrane proteins, although this effect decays following removal of the RF. Recently, it was shown that nanoparticle doping of RF irradiated water (NPD water produced a stabilized aqueous medium that maintained the characteristic properties of RF irradiated water for extended periods of time. Therefore, the ordering effect in water of the RF irradiation can now be studied in systems that required prolonged periods for analysis, such as eukaryotic cell culture. Since the formation of hybridoma cells involves the formation of a new membrane, a process that is affected by the surrounding aqueous environment, we tested these nanoparticle doped aqueous media formulations on hybridoma cell production. Results In this study, we tested the entire process of isolation and production of human monoclonal antibodies in NPD water as a means for further enhancing human monoclonal antibody isolation and production. Our results indicate an overall enhancement of hybridoma yield, viability, clonability and secretion. Furthermore, we have demonstrated that immortal cells proliferate faster whereas primary human fibroblasts

An Approach Toward Replacing Vanadium: A Single Organic Molecule for the Anode and Cathode of an Aqueous Redox-Flow Battery.

Science.gov (United States)

Janoschka, Tobias; Friebe, Christian; Hager, Martin D; Martin, Norbert; Schubert, Ulrich S

2017-04-01

By combining a viologen unit and a 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) radical in one single combi-molecule, an artificial bipolar redox-active material, 1-(4-(((1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)oxy)carbonyl)benzyl)-1'-methyl-[4,4'-bipyridine]-1,1'-diium-chloride ( VIOTEMP ), was created that can serve as both the anode (-0.49 V) and cathode (0.67 V vs. Ag/AgCl) in a water-based redox-flow battery. While it mimics the redox states of flow battery metals like vanadium, the novel aqueous electrolyte does not require strongly acidic media and is best operated at pH 4. The electrochemical properties of VIOTEMP were investigated by using cyclic voltammetry, rotating disc electrode experiments, and spectroelectrochemical methods. A redox-flow battery was built and the suitability of the material for both electrodes was demonstrated through a polarity-inversion experiment. Thus, an organic aqueous electrolyte system being safe in case of cross contamination is presented.

Robust binding between carbon nitride nanosheets and a binuclear ruthenium(II) complex enabling durable, selective CO{sub 2} reduction under visible light in aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Kuriki, Ryo; Ishitani, Osamu; Maeda, Kazuhiko [Department of Chemistry, School of Science, Tokyo Institute of Technology (Japan); Yamamoto, Muneaki; Yoshida, Tomoko [Advanced Research Institute for Natural Science and Technology, Osaka City University (Japan); Higuchi, Kimitaka; Yamamoto, Yuta; Akatsuka, Masato; Yagi, Shinya [Institute of Materials and Systems for Sustainability, Nagoya University (Japan); Lu, Daling [Suzukakedai Materials Analysis Division, Technical Department, Tokyo Institute of Technology, Yokohama (Japan)

2017-04-18

Carbon nitride nanosheets (NS-C{sub 3}N{sub 4}) were found to undergo robust binding with a binuclear ruthenium(II) complex (RuRu') even in basic aqueous solution. A hybrid material consisting of NS-C{sub 3}N{sub 4} (further modified with nanoparticulate Ag) and RuRu' promoted the photocatalytic reduction of CO{sub 2} to formate in aqueous media, in conjunction with high selectivity (approximately 98 %) and a good turnover number (>2000 with respect to the loaded Ru complex). These represent the highest values yet reported for a powder-based photocatalytic system during CO{sub 2} reduction under visible light in an aqueous environment. We also assessed the desorption of RuRu' from the Ag/C{sub 3}N{sub 4} surface, a factor that can contribute to a loss of activity. It was determined that desorption is not induced by salt additives, pH changes, or photoirradiation, which partly explains the high photocatalytic performance of this material. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

Media identities and media-influenced indentifications Visibility and identity recognition in the media

Directory of Open Access Journals (Sweden)

Víctor Fco. Sampedro Blanco

2004-10-01

Full Text Available The media establish, in large part, the patterns of visibility and public recognition of collective identities. We define media identities as those that are the object of production and diffusion by the media. From this discourse, the communities and individuals elaborate media-influenced identifications; that is, processes of recognition or banishment; (rearticulating the identity markers that the media offer with other cognitive and emotional sources. The generation and appropriation of the identities are subjected to a media hierarchisation that influences their normalisation or marginalisation. The identities presented by the media and assumed by the audience as part of the official, hegemonic discourse are normalised, whereas the identities and identifications formulated in popular and minority terms are marginalised. After presenting this conceptual and analytical framework, this study attempts to outline the logics that condition the presentation, on the one hand, andthe public recognition, on the other hand, of contemporary identities.

Sintesis dan Karakterisasi Polianilina Doping Asam Klorida dengan Metode Interfasial

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Iman Rahayu

2016-08-01

Full Text Available The growing interest in nanostructured conducting polymers is caused by expanding area of their practical application. Conducting polymers can be used in new electronic devices (transistors, displays, sensors, energy storage and memory cells, materials for shielding electromagnetic irradiation, inhibition of corrosion, membrane constructing, catalysis and medicine. The studies of polyaniline (PANI and other conducting polymers have shown that they possess semiconducting properties. Due to its high stability and unique complex of properties, PANI was the first among conducting polymers to be used in practice as an electrode material for batteries, as a corrosion inhibitor and detecting material for sensors. PANI without dopant material possesses controlled conductivity 10-10 S∙cm-1. PANI was synthesized by the interfacial method by oxidation of aniline with ammonium peroxydisulfate (APS as an oxidant in an immiscible organic/aqueous biphasic system, with hydrochloric acid as dopant. An organic phase contained aniline dissolved in toluene, while the oxidant was dissolved in acid. The produced PANIs have conductivities in the range 0.03-0.07 S.cm−1. Their nanofiber morphology was confirmed by scanning electron microscopy (SEM. Molecular structure of synthesized PANIs was investigated by FTIR Spectroscopy. DOI :http://dx.doi.org/10.15408/jkv.v0i0.3143

Search for chemical separations of the element 106 homologues in HF and HF-HCl media

International Nuclear Information System (INIS)

Trubert, D.; Monroy-Guzman, F.; Hussonnois, M.; Brillard, L.; Le Naour, C.; Constantinescu, O.

1996-01-01

In order to study the chemical properties of element 263 106 in aqueous media, fast, efficient and reproducible chromatographic separations were tested on its assumed homologous: Mo, W and U. Corroborative static and dynamic off-line experiments have shown that after fixation of these three elements on anion-exchange resin in HF medium, selective elution could be achieved by using suitable concentration of HCl - HF and HCl solutions. Separations of short-lived W isotopes, produced through heavy ion irradiation were also performed on-line. (author). 27 refs., 14 figs

Final report on CCQM-K27.2: Second Subsequent study: determination of ethanol in aqueous media

Science.gov (United States)

Schantz, Michele M.; Parris, Reenie M.; May, Willie E.; Rosso, Adriana; Puglisi, Celia; Marques Rodrigues Caixeiro, Janaína; Massiff, Gabriela; Camacho Frías, Evangelina; Pérez Urquiza, Melina; Archer, Marcellé; Visser, M. S.; deVos, Betty-Jayne

2013-01-01

Ethanol is important both forensically ('drunk driving' or driving while under the influence, 'DWI', regulations) and commercially (alcoholic beverages). Blood- and breath-alcohol testing can be imposed on individuals operating private vehicles such as cars, boats or snowmobiles, or operators of commercial vehicles like trucks, planes and ships. The various levels of blood alcohol that determine whether these operators are considered legally impaired vary depending on the circumstances and locality. Accurate calibration and validation of instrumentation is critical in areas of forensic testing where quantitative analysis directly affects the outcome of criminal prosecutions, as is the case with the determination of ethanol in blood and breath. Additionally, the accurate assessment of the alcoholic content of beverages is a commercially important commodity. In 2002, the CCQM conducted a key comparison (CCQM-K27) for the determination of ethanol in aqueous matrix with nine participants. A report on this project has been approved by the CCQM and can be found at the BIPM website. CCQM-K27 comprised three samples, one at low mass fraction of ethanol in water (nominal concentration of 0.8 mg/g), one at high level (nominal concentration of 120 mg/g) and one wine matrix (nominal concentration of 81 mg/g). Overall agreement among eight participants using gas chromatography with flame ionization detection (GC-FID), titrimetry, isotope dilution gas chromatography/mass spectrometry (GC-IDMS) and gas chromatography-combustion-isotope ratio mass spectrometry (ID-GC-C-IRMS) was good. The ninth participant used a headspace GC-FID method that had not been validated in an earlier pilot study (CCQM-P35). A follow-on key comparison, CCQM-K27-Subsequent, was initiated in 2003 to accommodate laboratories that had not been ready to benchmark their methods in the original CCQM-K27 study or that wished to benchmark a different method. Four levels of ethanol in water were used in the

Spectrophotometric determination of trace amount of uranium (VI) in different aqueous and organic streams of nuclear fuel processing using 2-(5-bromo-2-pyridylazo-5-diethylaminophenol)

International Nuclear Information System (INIS)

Das, S.K.; Kedari, C.S.; Tripathi, S.C.

2010-01-01

Present investigation describes the development of a spectrophotometric method for trace level determination of U(VI) encountered during the process of nuclear fuel fabrication and reprocessing industries. A chromogenic reagent, 2-(5-bromo-2-pyridylazo-5-diethylaminophenol) (Br-PADAP) is used to complex with U(VI) under optimized solution conditions. The absorption maxima of the uranyl Br-PADAP complex at 578 nm is computed to be 73540 ± 1438 for U-Br-PADAP solution containing 20% ethanol (in aqueous sample media) and 58216 ± 1208 for U-Br-PADAP solution containing 80% ethanol (for organic sample media). Employing suitable sample treatment methods, the scope of analytical method has been widened to permit accurate determination of U(VI) in the samples with variation in the relative compositions of Th(IV), Pu(IV) and Fe(III). The method is applicable to samples matrices with, acidic, alkaline highly salted media. Effect of commonly associated ionic species on the optical density of U-Br-PADAP is determined. Depending on the extent of the interfering impurities present, the method permits estimation of U(VI) either direct or after its selective extraction into tri-octyl phosphine oxide dissolved in cyclohexane. The method is precise with <5% standard error and can be used for the estimation of uranium in organic as well as in aqueous samples. The method has been validated for quantitative determination of uranium extracted in the organic phase comprising of heavy metal extractants like TBP, HDEHP, PC-88A and Aliquot 336. (author)

High energy electron beam inactivation of lactate dehydrogenase suspended in different aqueous media

International Nuclear Information System (INIS)

Hategan, A.; Popescu, A.; Butan, C.; Oproiu, C.; Hategan, D.; Morariu, V.V.

1999-01-01

The direct and indirect effects of 5 MeV electron beam irradiation in the range (0-400 Gy) at 20 degC, 0 degC, -3 degC and -196 degC, as well as the influence of the aqueous suspending medium (ultrapure water and heavy water) on the total enzymatic activity of lactate dehydrogenase (LDH) have been studied. Our results showed an exponential decrease on the enzymatic activity of irradiated LDH, at all irradiation temperatures, independently of the direct or indirect action of radiation. The temperature gradient used to lower the temperature of the samples to -196 degC drastically influences the results. Freeze-thawing in two steps down to -196 degC protects LDH to radiation, in the dose range used. The data obtained here inform on the high energy electrons effects on the enzymatic activity loss during irradiation and during thawing, when the subsequent growth of the water crystals influences the three dimensional structure of the enzyme. A 99.98% concentration of D 2 O in the suspending medium of the enzyme decreases the global enzymatic activity, but reduces the rate of radiation inactivation of the enzyme. The rate of radiation inactivation of the enzyme suspended in ultrapure water is reduced when compared to the enzyme suspended in bidistilled water, but compared to the D 2 O suspended enzyme is lightly increased. (author)

Nanoparticle dispersion in environmentally relevant culture media: a TiO2 case study and considerations for a general approach

International Nuclear Information System (INIS)

Horst, Allison M.; Ji, Zhaoxia; Holden, Patricia A.

2012-01-01

Nanoparticle exposure in toxicity studies requires that nanoparticles are bioavailable by remaining highly dispersed in culture media. However, reported dispersion approaches are variable, mostly study-specific, and not transferable owing to their empirical basis. Furthermore, many published approaches employ proteinaceous dispersants in rich laboratory media, both of which represent end members in environmental scenarios. Here, a systematic approach was developed to disperse initially agglomerated TiO 2 nanoparticles (Aeroxide® TiO 2 P25, Evonik, NJ; primary particle size range 6.4–73.8 nm) in oligotrophic culture medium for environmentally relevant bacterial toxicity studies. Based on understanding particle–particle interactions in aqueous media and maintaining environmental relevance, the approach involves (1) quantifying the relationship between pH and zeta potential to determine the point of zero charge of select nanoparticles in water; (2) nominating, then testing and selecting, environmentally relevant stabilizing agents; and (3) dispersing via “condition and capture” whereby stock dry powder nanoparticles are sonicated in pre-conditioned (with base, or acid, plus stabilizing agent) water, then diluted into culture media. The “condition and capture” principle is transferable to other nanoparticle and media chemistries: simultaneously, mechanically and electrostatically, nanoparticles can be dispersed with surrounding stabilizers that coat and sterically hinder reagglomeration in the culture medium.

Benzimidazole acrylonitriles as multifunctional push-pull chromophores: Spectral characterisation, protonation equilibria and nanoaggregation in aqueous solutions

Science.gov (United States)

Horak, Ema; Vianello, Robert; Hranjec, Marijana; Krištafor, Svjetlana; Zamola, Grace Karminski; Steinberg, Ivana Murković

2017-05-01

Heterocyclic donor-π-acceptor molecular systems based on an N,N-dimethylamino phenylacrylonitrile benzimidazole skeleton have been characterised and are proposed for potential use in sensing applications. The benzimidazole moiety introduces a broad spectrum of useful multifunctional properties to the system including electron accepting ability, pH sensitivity and compatibility with biomolecules. The photophysical characterisation of the prototropic forms of these chromophores has been carried out in both solution and on immobilisation in polymer films. The experimental results are further supported by computational determination of pKa values. It is noticed that compound 3 forms nanoaggregates in aqueous solutions with aggregation-induced emission (AIE) at 600 nm. All the systems demonstrate spectral pH sensitivity in acidic media which shifts towards near-neutral values upon immobilisation in polymer films or upon aggregation in an aqueous environment (compound 3). The structure-property relationships of these functional chromophores, involving their spectral characteristics, acid-base equilibria, pKa values and aggregation effects have been determined. Potential applications of the molecules as pH and biomolecular sensors are proposed based on their pH sensitivity and AIE properties.

Komunikasi Krisis di Era New Media dan Social Media

OpenAIRE

Prastya, Narayana Mahendra

2016-01-01

New media and social media have changed the practice of public relations. One area that changed is crisis communication. Because of these new technologies, crisis can be more complex. The pace of information, the uncertainty, and the rumors, are increasing. Public relations practitioners should include the new media and social media use in their crisis communication plan. Before doing that, public relations practitioners should change their mindset about social media and new media. The first ...

Separation and preconcentration of Arsenic(III ions from aqueous media by adsorption on MWCNTs

Directory of Open Access Journals (Sweden)

Nahid Tavakkoli

2017-05-01

Full Text Available A simple and sensitive method using mini-column packed with multi-walled carbon nanotubes (MWCNTs combined with graphite furnace atomic absorption spectrometry (GFAAS for preconcentration and determination of ultra trace amounts of As(III in an aqueous medium is proposed. The procedure is based on the solid phase extraction of the As(III-sodium diethyldithiocarbamate (As-NaDDTC chelate on MWCNTs. Various parameters such as the effect of pH, eluent type and volume, amount of sorbent, and matrix effects on the quantitative recoveries of analyte ions were evaluated. It was found that sorption is quantitative and desorption occurs with 4.0 mL of 3.0 mol L−1 HNO3 in acetone. The limit of detection of the method was 0.008 ng mL−1 for GFAAS with enrichment factor of 125 and the relative standard deviation (RSD 0.97% (n = 8, C = 10 ng mL−1. This method has been applied to the determination of ultra trace As(III in water and rice plant and its ash successfully.

Selective fluorescence detection of Cu{sup 2+} in aqueous solution and living cells

Energy Technology Data Exchange (ETDEWEB)

Saleem, Muhammad; Lee, Ki-Hwan, E-mail: khlee@kongju.ac.kr

2014-01-15

A rhodamine B semicarbazide 3 was synthesized by the reaction of rhodamine B acid chloride 2 with hydrazine carboxamide hydrochloride under reflux with triethyl amine in acetonitrile. It was used as selective fluorescent and colorimetric sensor for visual detection of Cu{sup 2+} over competitive ions (Fe{sup 3+},Fe{sup 2+}, Cr{sup 3+}, Cd{sup 2+}, Pb{sup 2+}, Zn{sup 2+}, Hg{sup 2+}, Co{sup 2+}, Ni{sup 2+}, Ca{sup 2+}, Mg{sup 2+}, Ag{sup 2+}, Mn{sup 2+}, Sr{sup 2+}, Cs{sup 2+}, Na{sup +}, K{sup +}, Li{sup +}) in aqueous methanol (1:1, v/v), exhibiting a fast response time, less than few second and a detection limit of 1.6×10{sup −7} mol/L at neutral pH. The proposed sensing system can be successfully applicable for determination of Cu{sup 2+} in waste water samples showing turn on fluorescence response and for further monitoring of intracellular Cu{sup 2+} levels in living cells with high sensitivity and selectivity at micro molar level concentrations using confocal fluorescence spectroscopy. The synthesis of probe 3 was confirmed by {sup 1}H NMR, {sup 13}C NMR and mass spectrometric analysis. -- Highlights: • New chemosensor rhodamine B semicarbazide 3 was synthesized. • Addition of Cu{sup +2} ion into aqueous solution of probe 3 gave visual color changes as well as fluorescent off/on observations. • The proposed spirolactam ring opening mechanism of the synthesized probe triggered by copper ion was revealed by using mass spectrum. • High selectivity and sensitivity of probe 3 towards Cu{sup +2} are excellent enough to detect micromolar level of Cu{sup +2} ion even in aqueous media and living cells.

Aqueous colloidal processing of fluorapatite bodies

International Nuclear Information System (INIS)

Albano, Maria P.; Garrido, Liliana B.

2011-01-01

In order to produce stable aqueous fluorapatite (FA) suspensions, its surface reactivity in an aqueous solution having two initial pH values with a concentration of ammonium polyacrylate (NH_4PA) was investigated as a function of time. The influence of the slip viscosity on the casting rate and the microstructure of the resultant green slip cast compacts was determined. Upon the FA introduction in the aqueous solutions, an initial release of F anions located at the surface was found, which was not dependent of the pH and the presence of dispersant. The increase in the initial pH of the solution above 7 and/or the addition of NH_4PA markedly reduced the Ca"+"+/ H"+ exchange reaction rate. As a result, well-stabilized concentrated aqueous suspensions could be obtained at pH close to 9. The greater permeability of cakes produced from slips with high viscosity values (0.5 wt% PVA) increased the casting rate. (author)

Media education and media enlightenment as attributes of information society

Directory of Open Access Journals (Sweden)

Лилия Борисовна Белоглазова

2014-12-01

Full Text Available The article deals with the problem of the functioning of media-education and media-enlightenment in modern society. Focuses on the impact of this socio-cultural phenomenon on consciousness of members of the Information Society. Are the main characteristics of media-education and media-education and media-enlightenment. Concludes that media-education and media-enlightenment forms unscientific and anti-scientific thinking and style speech.

Ternary rare earth sulfide CaCe2S4: Synthesis and characterization of stability, structure, and photoelectrochemical properties in aqueous media

Science.gov (United States)

Sotelo, Paola; Orr, Melissa; Galante, Miguel Tayar; Hossain, Mohammad Kabir; Firouzan, Farinaz; Vali, Abbas; Li, Jun; Subramanian, Mas; Longo, Claudia; Rajeshwar, Krishnan; Macaluso, Robin T.

2018-06-01

A red-orange rare earth ternary chalcogenide, CaCe2S4, was prepared in powder form by solid-state synthesis. The structural details of this compound were determined by powder X-ray diffraction. The optical band gap of CaCe2S4 was determined by diffuse reflectance spectroscopy (DRS) to be 2.1 eV, consistent with the observed red-orange color. Quantitative colorimetry measurements also support the observed color and band gap of CaCe2S4. Both direct and indirect optical transitions were gleaned from Tauc analyses of the DRS data. Photoelectrochemistry experiments on CaCe2S4 films showed n-type semiconductor behavior. Analyses of these data via the Butler-Gärtner model afforded a flat-band potential of - 0.33 V (vs. Ag/AgCl/KCl 4 M) in pH 9 aqueous sulfite electrolyte. The potential and limitations of this material for solar water splitting and photocatalytic environmental remediation (e.g., dye photodegradation) are finally presented against the backdrop of its photoelectrochemical stability and surface hole transfer kinetics in aqueous electrolytes.

Sensitive Media

Directory of Open Access Journals (Sweden)

Malinowska Anna

2017-12-01

Full Text Available The paper engages with what we refer to as “sensitive media,” a concept associated with developments in the overall media environment, our relationships with media devices, and the quality of the media themselves. Those developments point to the increasing emotionality of the media world and its infrastructures. Mapping the trajectories of technological development and impact that the newer media exert on human condition, our analysis touches upon various forms of emergent affect, emotion, and feeling in order to trace the histories and motivations of the sensitization of “the media things” as well as the redefinition of our affective and emotional experiences through technologies that themselves “feel.”

Evaluation of biosurfactants grown in corn oil by Rhodococcus rhodochrous on removing of heavy metal ion from aqueous solution

International Nuclear Information System (INIS)

Suryanti, Venty; Hastuti, Sri; Pujiastuti, Dwi

2016-01-01

The potential application of biosurfactants to remove heavy metal ion from aqueous solution by batch technique was examined. The glycolipids type biosurfactants were grown in a media containing of 20% v/v corn oil with 7 days of fermentation by Rhodococcus rhodochrous. The biosurfactants reduced the surface tension of water of about 51% from 62 mN/m to 30 mN/m. The biosurfactant increased the E24 of water-palm oil emulsion of about 55% from 43% to 97% and could maintain this E24 value of above 50% for up to 9 days. Heavy metal ion removal, in this case cadmium ion, by crude and patially purified biosurfactants has been investigated from aqueous solution at pH 6. Adsorption capacity of Cd(II) ion by crude biosurfactant with 5 and 10 minutes of contact times were 1.74 and 1.82 mg/g, respectively. Additionally, the adsorption capacity of Cd(II) ion by partially purified biosurfactant with 5 and 10 minutes of contact times were 0.79 and 1.34 mg/g, respectively. The results demonstrated that the adsorption capacity of Cd(II) ion by crude biosurfactant was higher than that of by partially purified biosurfactant. The results suggested that the biosurfactant could be used in the removal of heavy metal ions from aqueous solution

Evaluation of biosurfactants grown in corn oil by Rhodococcus rhodochrous on removing of heavy metal ion from aqueous solution

Science.gov (United States)

Suryanti, Venty; Hastuti, Sri; Pujiastuti, Dwi

2016-02-01

The potential application of biosurfactants to remove heavy metal ion from aqueous solution by batch technique was examined. The glycolipids type biosurfactants were grown in a media containing of 20% v/v corn oil with 7 days of fermentation by Rhodococcus rhodochrous. The biosurfactants reduced the surface tension of water of about 51% from 62 mN/m to 30 mN/m. The biosurfactant increased the E24 of water-palm oil emulsion of about 55% from 43% to 97% and could maintain this E24 value of above 50% for up to 9 days. Heavy metal ion removal, in this case cadmium ion, by crude and patially purified biosurfactants has been investigated from aqueous solution at pH 6. Adsorption capacity of Cd(II) ion by crude biosurfactant with 5 and 10 minutes of contact times were 1.74 and 1.82 mg/g, respectively. Additionally, the adsorption capacity of Cd(II) ion by partially purified biosurfactant with 5 and 10 minutes of contact times were 0.79 and 1.34 mg/g, respectively. The results demonstrated that the adsorption capacity of Cd(II) ion by crude biosurfactant was higher than that of by partially purified biosurfactant. The results suggested that the biosurfactant could be used in the removal of heavy metal ions from aqueous solution.

Evaluation of biosurfactants grown in corn oil by Rhodococcus rhodochrous on removing of heavy metal ion from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Suryanti, Venty, E-mail: venty@mipa.uns.ac.id; Hastuti, Sri; Pujiastuti, Dwi [Department of Chemistry, Faculty of Mathematics and Natural Sciences, Sebelas Maret University Jl. Ir. Sutami 36A, Surakarta, Central Java 57126 (Indonesia)

2016-02-08

The potential application of biosurfactants to remove heavy metal ion from aqueous solution by batch technique was examined. The glycolipids type biosurfactants were grown in a media containing of 20% v/v corn oil with 7 days of fermentation by Rhodococcus rhodochrous. The biosurfactants reduced the surface tension of water of about 51% from 62 mN/m to 30 mN/m. The biosurfactant increased the E24 of water-palm oil emulsion of about 55% from 43% to 97% and could maintain this E24 value of above 50% for up to 9 days. Heavy metal ion removal, in this case cadmium ion, by crude and patially purified biosurfactants has been investigated from aqueous solution at pH 6. Adsorption capacity of Cd(II) ion by crude biosurfactant with 5 and 10 minutes of contact times were 1.74 and 1.82 mg/g, respectively. Additionally, the adsorption capacity of Cd(II) ion by partially purified biosurfactant with 5 and 10 minutes of contact times were 0.79 and 1.34 mg/g, respectively. The results demonstrated that the adsorption capacity of Cd(II) ion by crude biosurfactant was higher than that of by partially purified biosurfactant. The results suggested that the biosurfactant could be used in the removal of heavy metal ions from aqueous solution.

Investigation of the promoting effect of Mn on a Pt/C catalyst for the steam and aqueous phase reforming of glycerol

Energy Technology Data Exchange (ETDEWEB)

Bossola, Filippo; Pereira-Hernández, Xavier Isidro; Evangelisti, Claudio; Wang, Yong; Dal Santo, Vladimiro

2017-05-01

The catalytic performances in steam reforming (SR) and aqueous phase reforming (APR) of glycerol of a bimetallic Pt-Mn catalyst supported on activated carbon are investigated and correlated with the surface properties of the catalyst. Under SR conditions, Mn showed a significant promoting effect over Pt/C, both in terms of hydrogen production rate and conversion, with a higher selectivity toward the glycerol dehydration products. Upon addition of Mn the amount of strong Lewis acid sites increased, promoting the dehydration of glycerol and favoring the CAO over CAC cleavage at expenses of hydrogen selectivity. Conversely, under APR conditions, a slightly higher hydrogen selectivity and only minimal enhancement in hydrogen production were found, while the products selectivity was comparable to Pt/C. Most of Mn leached into the aqueous media, but the remaining (<5% of the fresh parent sample) might be alloyed with Pt and promote the CO desorption from neighbor Pt sites.

Social Media Sites

Science.gov (United States)

Media Sites Site Registration Contact Us Search AF.mil: Home > AF Sites > Social Media Sites Social Media Welcome to the Air Force social media directory! The directory is a one-stop shop of official Air Force social media pages across various social media sites. Social media is all about

Stereotypes in media and media literacy among young people

Directory of Open Access Journals (Sweden)

Đerić Ivana

2006-01-01

Full Text Available Young people, the most common consumers of media content, bear out the view that media shapes people’s lives. Therefore we must not underestimate the effect media exerts on young people’s values and behavioral patterns. Television is the medium which draws children and young people for the greatest part of their free time. Regardless whether television programs are described as positive or negative, whether they abound with stereotypes or not, it is important that young people develop a critical attitude towards them so that they may resist different forms of media manipulation. The paper discusses how stereotypes are generated and used by media and the manners in which stereotypical concepts affect young people’s attitudes. It highlights the importance of the development of media literacy which implies a critical attitude towards media images and discourses, the development of criteria for the selection and evaluation of information broadcast by media, the development of skills in interpreting and understanding stereotypical concepts and familiarity with alternative forms of media culture. The paper draws special attention to the issue of media education. The conclusion is that schools should offer media literacy as part of their curriculum and in it possible solutions to the problems discussed. .

Electrochemical oxidation of synthetic tannery wastewater in chloride-free aqueous media

International Nuclear Information System (INIS)

Costa, Carla Regina; Montilla, Francisco; Morallon, Emilia; Olivi, Paulo

2010-01-01

The electrochemical treatment of a synthetic tannery wastewater, prepared with several compounds used by finishing tanneries, was studied in chloride-free media. Boron-doped diamond (Si/BDD), antimony-doped tin dioxide (Ti/SnO 2 -Sb), and iridium-antimony-doped tin dioxide (Ti/SnO 2 -Sb-Ir) were evaluated as anode. The influence of pH and current density on the treatment was assessed by means of the parameters used to measure the level of organic contaminants in the wastewater; i.e., total phenols, chemical oxygen demand (COD), total organic carbon (TOC), and absorbance. Results showed that faster decrease in these parameters occurred when the Si/BDD anode was used. Good results were obtained with the Ti/SnO 2 -Sb anode, but its complete deactivation was reached after 4 h of electrolysis at 25 mA cm -2 , indicating that the service life of this electrode is short. The Ti/SnO 2 -Sb-Ir anode is chemically and electrochemically more stable than the Ti/SnO 2 -Sb anode, but it is not suitable for the electrochemical treatment under the studied conditions. No significant changes were observed for electrolyses performed at different pH conditions with Si/BDD, and this electrode led to almost complete mineralization after 4 h of electrolysis at 100 mA cm -2 . The increase in current density resulted in faster wastewater oxidation, with lower current efficiency and higher energy consumption. Si/BBD proved to be the best electrodic material for the direct electrooxidation of tannery wastewaters.

27 CFR 21.96 - Ammonia, aqueous.

Science.gov (United States)

2010-04-01

... 27 Alcohol, Tobacco Products and Firearms 1 2010-04-01 2010-04-01 false Ammonia, aqueous. 21.96 Section 21.96 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT... Ammonia, aqueous. (a) Alkalinity. Strongly alkaline to litmus. (b) Ammonia content. 27 to 30 percent by...

Ce–Fe-modified zeolite-rich tuff to remove Ba{sup 2+}-like {sup 226}Ra{sup 2+} in presence of As(V) and F{sup −} from aqueous media as pollutants of drinking water

Energy Technology Data Exchange (ETDEWEB)

Olguín, María Teresa, E-mail: teresa.olguin@inin.gob.mx [Department of Chemical & Materials Engineering, New Mexico State University, P.O. Box 30001, MSC 3805, Las Cruces, NM 88003 (United States); Departamento de Química, Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, Col. Escandón, Delegación Miguel Hidalgo, C.P. 11801, México D.F. (Mexico); Deng, Shuguang [Department of Chemical & Materials Engineering, New Mexico State University, P.O. Box 30001, MSC 3805, Las Cruces, NM 88003 (United States)

2016-01-25

Graphical abstract: Ba{sup 2+}-like {sup 226}Ra{sup 2+}, As(V) and F{sup −} simultaneous removal from aqueous media by Ce–Fe-modified natural zeolites. - Highlights: • The metallic species which modified the zeolite change the textural properties. • The pH{sub pzc} is acid for ZUSCeFe and neutral for ZUSNa. • The Linear model describes the Ba{sup 2+}-like {sup 226}Ra{sup 2+} sorption by ZUSNa and ZUSCeFe. • K{sub d} is highest for Ba{sup 2+-} like {sup 226}Ra{sup 2+}-As(V)-F{sup -} solution in contact with ZUSCeFe. • The ZUSCeFe remove simultaneously Ba{sup 2+}-like {sup 226}Ra{sup 2+}, As(V) and F{sup −}. - Abstract: The sorption behavior of the Ba{sup 2+}-like {sup 226}Ra{sup 2+} in the presence of H{sub 2}AsO{sub 4}{sup −}/HAsO{sub 4}{sup 2−} and F{sup −} from aqueous media using Ce–Fe-modified zeolite-rich tuff was investigated in this work. The Na-modified zeolite-rich tuff was also considered for comparison purposes. The zeolite-rich tuff collected from Wyoming (US) was in contact with NaCl and CeCl{sub 3}–FeCl{sub 3} solutions to obtain the Na- and Ce–Fe-modified zeolite-rich tuffs (ZUSNa and ZUSCeFe). These zeolites were characterized by scanning electron microscopy and X-ray diffraction. The BET-specific surface and the points of zero charge were determined as well as the content of Na, Ce and Fe by neutron activation analysis. The textural characteristics and the point of zero charge were changed by the presence of Ce and Fe species in the zeolitic network. A linear model described the Ba{sup 2+}-like {sup 226}Ra{sup 2+} sorption isotherms and the distribution coefficients (K{sub d}) varied with respect to the metallic species present in the zeolitic material. The As(V) oxianionic chemical species and F{sup −} affected this parameter when the Ba{sup 2+}-like {sup 226}Ra{sup 2+}-As(V)-F{sup −} solutions were in contact with ZUSCeFe. The H{sub 2}AsO{sub 4}{sup −}/HAsO{sub 4}{sup 2−} and F{sup −} were adsorbed by ZUSCe

Aqueous foam toxicology evaluation and hazard review

Energy Technology Data Exchange (ETDEWEB)

Archuleta, M.M.

1995-10-01

Aqueous foams are aggregates of bubbles mechanically generated by passing air or other gases through a net, screen, or other porous medium that is wetted by an aqueous solution of surface-active foaming agents (surfactants). Aqueous foams are important in modem fire-fighting technology, as well as for military uses for area denial and riot or crowd control. An aqueous foam is currently being developed and evaluated by Sandia National Laboratories (SNL) as a Less-Than-Lethal Weapon for the National Institute of Justice (NIJ). The purpose of this study is to evaluate the toxicity of the aqueous foam developed for the NIJ and to determine whether there are any significant adverse health effects associated with completely immersing individuals without protective equipment in the foam. The toxicity of the aqueous foam formulation developed for NIJ is determined by evaluating the toxicity of the individual components of the foam. The foam is made from a 2--5% solution of Steol CA-330 surfactant in water generated at expansion ratios ranging from 500:1 to 1000:1. SteoI CA-330 is a 35% ammonium laureth sulfate in water and is produced by Stepan Chemical Company and containing trace amounts (<0.1%) of 1,4-dioxane. The results of this study indicate that Steol CA-330 is a non-toxic, mildly irritating, surfactant that is used extensively in the cosmetics industry for hair care and bath products. Inhalation or dermal exposure to this material in aqueous foam is not expected to produce significant irritation or systemic toxicity to exposed individuals, even after prolonged exposure. The amount of 1,4-dioxane in the surfactant, and subsequently in the foam, is negligible and therefore, the toxicity associated with dioxane exposure is not significant. In general, immersion in similar aqueous foams has not resulted in acute, immediately life-threatening effects, or chronic, long-term, non-reversible effects following exposure.

Photolysis of sulfamethoxypyridazine in various aqueous media: Aerobic biodegradation and identification of photoproducts by LC-UV–MS/MS

Energy Technology Data Exchange (ETDEWEB)

Khaleel, Nareman D.H., E-mail: drndahshan@yahoo.com [Sustainable Chemistry and Material Resources, Institute of Sustainable and Environmental Chemistry, Leuphana University Lüneburg, C13, DE-21335 Lüneburg (Germany); Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia 41522 (Egypt); Mahmoud, Waleed M.M. [Sustainable Chemistry and Material Resources, Institute of Sustainable and Environmental Chemistry, Leuphana University Lüneburg, C13, DE-21335 Lüneburg (Germany); Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia 41522 (Egypt); Hadad, Ghada M.; Abdel-Salam, Randa A. [Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia 41522 (Egypt); Kümmerer, Klaus, E-mail: Klaus.Kuemmerer@uni.leuphana.de [Sustainable Chemistry and Material Resources, Institute of Sustainable and Environmental Chemistry, Leuphana University Lüneburg, C13, DE-21335 Lüneburg (Germany)

2013-01-15

Highlights: ► Sulfonamides are one of the most extensively used antibiotics in human and veterinary medicine. ► Sulfamethoxypyridazine (SMP) underwent photodegradation in three different media. ► SMP was not readily biodegradable. ► SMP and some of its degradation products were identified by LC-UV–MS/MS. -- Abstract: Sulfonamides are one of the most frequently used antibiotics worldwide. Therefore, mitigation processes such as abiotic or biotic degradation are of interest. Photodegradation and biodegradation are the potentially significant removal mechanisms for pharmaceuticals in aquatic environments. The photolysis of sulfamethoxypyridazine (SMP) using a medium pressure Hg-lamp was evaluated in three different media: Millipore water pH 6.1 (MW), effluent from sewage treatment plant pH 7.6 (STP), and buffered demineralized water pH 7.4 (BDW). Identification of transformation products (TPs) was performed by LC-UV–MS/MS. The biodegradation of SMP using two tests from the OECD series was studied: Closed Bottle test (OECD 301 D), and Manometric Respirometry test (OECD 301 F). In biodegradation tests, it was found that SMP was not readily biodegradable so it may pose a risk to the environment. The results showed that SMP was removed completely within 128 min of irradiation in the three media, and the degradation rate was different for each investigated type of water. However, dissolved organic carbon (DOC) was not removed in BDW and only little DOC removal was observed in MW and STP, thus indicating the formation of TPs. Analysis by LC-UV–MS/MS revealed new TPs formed. The hydroxylation of SMP represents the main photodegradation pathway.

Photolysis of sulfamethoxypyridazine in various aqueous media: Aerobic biodegradation and identification of photoproducts by LC-UV–MS/MS

International Nuclear Information System (INIS)

Khaleel, Nareman D.H.; Mahmoud, Waleed M.M.; Hadad, Ghada M.; Abdel-Salam, Randa A.; Kümmerer, Klaus

2013-01-01

Highlights: ► Sulfonamides are one of the most extensively used antibiotics in human and veterinary medicine. ► Sulfamethoxypyridazine (SMP) underwent photodegradation in three different media. ► SMP was not readily biodegradable. ► SMP and some of its degradation products were identified by LC-UV–MS/MS. -- Abstract: Sulfonamides are one of the most frequently used antibiotics worldwide. Therefore, mitigation processes such as abiotic or biotic degradation are of interest. Photodegradation and biodegradation are the potentially significant removal mechanisms for pharmaceuticals in aquatic environments. The photolysis of sulfamethoxypyridazine (SMP) using a medium pressure Hg-lamp was evaluated in three different media: Millipore water pH 6.1 (MW), effluent from sewage treatment plant pH 7.6 (STP), and buffered demineralized water pH 7.4 (BDW). Identification of transformation products (TPs) was performed by LC-UV–MS/MS. The biodegradation of SMP using two tests from the OECD series was studied: Closed Bottle test (OECD 301 D), and Manometric Respirometry test (OECD 301 F). In biodegradation tests, it was found that SMP was not readily biodegradable so it may pose a risk to the environment. The results showed that SMP was removed completely within 128 min of irradiation in the three media, and the degradation rate was different for each investigated type of water. However, dissolved organic carbon (DOC) was not removed in BDW and only little DOC removal was observed in MW and STP, thus indicating the formation of TPs. Analysis by LC-UV–MS/MS revealed new TPs formed. The hydroxylation of SMP represents the main photodegradation pathway

Effect of scenedesmus acuminatus green algae extracts on the development of Candida lipolytic yeast in gas condensate-containing media

Science.gov (United States)

Bilmes, B. I.; Kasymova, G. A.; Runov, V. I.; Karavayeva, N. N.

1980-01-01

Data are given of a comparative study of the growth and development as well as the characteristics of the biomass of the C. Lipolytica yeast according to the content of raw protein, protein, lipids, vitamins in the B group, and residual hydrocarbons during growth in media with de-aromatized gas-condensate FNZ as the carbon source with aqueous and alcohol extracts of S. acuminatus as the biostimulants. It is shown that the decoction and aqueous extract of green algae has the most intensive stimulating effect on the yeast growth. When a decoction of algae is added to the medium, the content of residual hydrocarbons in the biomass of C. lipolytica yeast is reduced by 4%; the quantity of protein, lipids, thamine and inositol with replacement of the yeast autolysate by the decoction of algae is altered little.

Media evolution and ‘epi-technic’ digital media: Media as cultural selection mechanisms

DEFF Research Database (Denmark)

Olesen, Mogens

2016-01-01

The explosive development of new digital media technologies is often described as a media evolution but hardly ever is the concept of ‘media evolution’ taken at face value. This article takes up that challenge by combining cultural evolution theories with medium theory. The article argues that bi...

Effect of a pulsed magnetic field on permeability of the cornea and sorption properties of the tissue structures and refractive media of the eye

International Nuclear Information System (INIS)

Skrinnik, A.V.

1986-01-01

The author attempts to obtain direct proof of increased permeability of the cornea and enhanced sorption properties of the tissue structures and refractive media of the eye under the influence of a pulsed magnetic field (MF). In the course of the investigation, the method of radioactive indication of two substances ( 35 S-streptomycin and 75 Se-methionine), widely used in opthalmologic practice, was used. The radioactivity of the working solution of the preparations was 300,000 cpm in 0.1 ml. Changes in the permeability of the cornea were assessed on the basis of changes in radioactivity of the aqueous humor. The concentration of 35 S-streptomycin in aqueous humor of the animals immediately after exposure to MF was significantly higher than in the control. Analysis of permeability of the cornea for 75 Se-methionine also showed increased penetration of radioactivity into the aqueous. The results are evidence of the greater penetrating power of 75 Se-methionine

Pertechnetate immobilization in aqueous media with hydrogen sulfide under anaerobic and aerobic environments

International Nuclear Information System (INIS)

Liu, Y.; Jurisson, S.; Terry, J.

2007-01-01

The basic chemistry for the immobilization of pertechnetate (TcO 4 - ) by hydrogen sulfide was investigated in aqueous solution under both aerobic and anaerobic environments. Pertechnetate immobilization was acid dependent, with accelerated rates and increased immobilization yields as the acid concentration increased. Oxygen had no effect under acidic conditions. Under anaerobic alkaline conditions, the pH, and therefore the speciation of sulfide, was the determining factor on the immobilization of pertechnetate. Only 53% of the TcO 4 - was immobilized at pH 8, while the yield increased to 83% at pH 9 as HS - became the dominant sulfide species. The immobilization yield then decreased to 73% at pH 13. No reaction was observed between TcO 4 - and sulfide under aerobic alkaline conditions, indicating that oxygen suppressed this reaction. Pertechnetate immobilization was found to be first order with respect to both sulfide and pertechnetate in acidic solutions, and in alkaline solution under anaerobic conditions. The results of stoichiometry studies and product analysis under alkaline anaerobic environments indicated that Tc 2 S 7 was obtained at pH 9. EXAFS (extended X-ray absorption fine structure) and XANES (X-ray absorption near edge structure) studies suggested that the samples obtained from acidic, aerobic solution and alkaline anaerobic solution were both Tc 2 S 7 . The stability of Tc 2 S 7 is affected by O 2 with accelerated dissolution at high pH. (orig.)

Chitosan-caffeic acid-genipin films presenting enhanced antioxidant activity and stability in acidic media.

Science.gov (United States)

Nunes, Cláudia; Maricato, Élia; Cunha, Ângela; Nunes, Alexandra; da Silva, José A Lopes; Coimbra, Manuel A

2013-01-02

The use of chitosan films has been limited due to their high degradability in aqueous acidic media. In order to produce chitosan films with high antioxidant activity and insoluble in acid solutions caffeic acid was grafted to chitosan by a radical mechanism using ammonium cerium (IV) nitrate (60 mM). Genipin was used as cross-linker. This methodology originated films with 80% higher antioxidant activity than the pristine film. Also, these films only lost 11% of their mass upon seven days immersion into an aqueous solution at pH 3.5 under stirring. The films surface wettability (contact angle 105°), mechanical properties (68 MPa of tensile strength and 4% of elongation at break), and thermal stability for temperatures lower than 300 °C were not significantly influenced by the covalent linkage of caffeic acid and genipin to chitosan. Due to their characteristics, mainly higher antioxidant activity and lower solubility, these are promising materials to be used as active films. Copyright © 2012 Elsevier Ltd. All rights reserved.

Analysis of plasma-mediated ablation in aqueous tissue

International Nuclear Information System (INIS)

Jiao Jian; Guo Zhixiong

2012-01-01

Plasma-mediated ablation using ultrafast lasers in transparent media such as aqueous tissues is studied. It is postulated that a critical seed free electron density exists due to the multiphoton ionization in order to trigger the avalanche ionization which causes ablation and during the avalanche ionization process the contribution of laser-induced photon ionization is negligible. Based on this assumption, the ablation process can be treated as two separate processes - the multiphoton and avalanche ionizations - at different time stages; so that an analytical solution to the evolution of plasma formation is obtained for the first time. The analysis is applied to plasma-mediated ablation in corneal epithelium and validated via comparison with experimental data available in the literature. The critical seed free-electron density and the time to initiate the avalanche ionization for sub-picosecond laser pulses are analyzed. It is found that the critical seed free-electron density decreases as the pulse width increases, obeying a t p -5.65 rule. This model is further extended to the estimation of crater size in the ablation of tissue-mimic polydimethylsiloxane (PDMS). The results match well with the available experimental measurements.

[New-type electrodeless excilamp for advanced treatment on nitrogen-heterocyclic compounds (NHCs) in aqueous solution].

Science.gov (United States)

Ye, Zhao-Lian; Wang, Bin; Lu, Juan-Juan; Li, Feng; Zhang, Ren-Xi

2012-03-01

A novel 206 nm excilamp generated by microwave-driven Kr/I2 mixtures was employed for nitrogen-heterocyclic compounds (NHCs) degradation in aqueous solution. The photodissociation efficiencies of indole and quinoline with 206 nm excilamp were estimated on the basis of removal efficiency of targeted compounds and the loss of total organic carbon (TOC). The results indicated that removal efficiency of 20 mg x L(-1) indole was as high as 62.0% after 80 min and TOC loss efficiency of 50.7% for 150 min. The irradiation time, initial concentration and pH value had some influences on quinoline degradation. Indole removal efficiency and TOC loss was markedly higher than that of quinoline under the same condition. The intermediates were identified qualitatively by gas chromatography/mass spectrum (GC/MS) with headspace sampling after they were extracted by rotary evaporator. GC/MS analysis indicated that indole and quinoline underwent ring-open dissociation under 206 nm irradiation, as a result, benzene, xylene, acetate, aldehyde, as well as ester compounds were formed, while indole aggregation reaction occurred during indole photodegradation. At last, degradation mechanisms of quinoline and indole in aqueous media with 206 nm excilamp were proposed on the basis of intermediates.

Synthesis of new annulated pyrano[2,3-d]pyrimidine derivatives using organo catalyst (DABCO in aqueous media

Directory of Open Access Journals (Sweden)

Ajmal R. Bhat

2017-01-01

Full Text Available A selective method for the synthesis of annulated pyrano[2,3-d]pyrimidines has been developed. It was shown that base catalysis is more efficient in this reaction, rather than acid catalysis as it is believed that 1,4-diazabicyclo[2.2.2]octane (DABCO is N-type base catalyst used for the synthesis of pyrano[2,3-d]pyramidine derivatives via one-pot three component condensation reactions of various aromatic aldehydes, active methylene compounds and barbituric acid in aqueous ethanol carried at normal temperature. The potential application of DABCO in organic synthesis increasing rapidly because of its reaction simplicity, less pollution, and minimum reaction time, high yields of the biological active products, uses less toxic solvents and low cost chemicals.

Synthesis and characterization of porous calcium phosphate; Sintesis y caracterizacion del fosfato de calcio poroso

Energy Technology Data Exchange (ETDEWEB)

Granados C, F.; Serrano G, J.; Bonifacio M, J. [ININ, 52750 La Marquesa, Estado de Mexico (Mexico)]. e-mail: fgc@nuclear.inin.mx

2007-07-01

The porous calcium phosphate was prepared by the continuous precipitation method using Ca(NO{sub 3}){sub 2}.4H{sub 2}O and NH{sub 4}H{sub 2}PO{sub 4} salts. The synthesized material was structurally and superficially characterized using the XRD, BET, IR TGA and SEM techniques. The obtained inorganic material was identified as calcium phosphate that presents a great specific area for what can be efficiently used as adsorbent material for adsorption studies in the radioactive wastes treatment present in aqueous solution. (Author)

Trolling new media: violent extremist groups recruiting through social media

OpenAIRE

Chang, Mark D.

2015-01-01

Approved for public release; distribution is unlimited With the advent and subsequent growth of several new media technologies, violent extremist groups have incorporated social media into recruiting strategies. How are violent extremist groups using social media for recruiting? This thesis explores several new media technologies—websites, blogs, social media, mobile phones, and online gaming—to determine if violent extremist groups rely on social media for recruiting. By comparing the com...

Media education.

Science.gov (United States)

Strasburger, Victor C

2010-11-01

The American Academy of Pediatrics recognizes that exposure to mass media (eg, television, movies, video and computer games, the Internet, music lyrics and videos, newspapers, magazines, books, advertising) presents health risks for children and adolescents but can provide benefits as well. Media education has the potential to reduce the harmful effects of media and accentuate the positive effects. By understanding and supporting media education, pediatricians can play an important role in reducing harmful effects of media on children and adolescents.

Technetium electrodeposition from aqueous formate solutions at graphite electrode: electrochemical study

International Nuclear Information System (INIS)

Maslennikov, A.; Peretroukhine, V.; Masson, M.; Lecomte, M.

1999-01-01

Recovery of technetium from aqueous formate buffer solutions of ionic strength μ = 1.0 was studied in the pH interval from 1.6 to 7.5 at graphite cathode in an electrolytic cell with separated compartments was studied, using cyclic voltammetry (CV) and inverse stripping voltammetry (ISV) techniques. It has been shown that Tc electrodeposition process becomes possible at the potentials of graphite cathode E cath. 1/2 = -0.72±0.02 V/SCE and was pH independent in the interval pH = 3.46-7.32. Mechanism of electrodeposition, including Tc(VII)/Tc(IV) reduction in the solution followed by Tc(IV) hydrolysis at the electrode surface with formation of hydrated Tc oxide cathodic deposit has been proposed. The further precision of the Tc(VII) electrochemical reduction mechanism in formate buffer media and optimization of the electrodeposition process seems to be possible using additional analytical facilities except electrochemical methods. (orig.)

Inverse hydrochemical models of aqueous extracts tests

Energy Technology Data Exchange (ETDEWEB)

Zheng, L.; Samper, J.; Montenegro, L.

2008-10-10

Aqueous extract test is a laboratory technique commonly used to measure the amount of soluble salts of a soil sample after adding a known mass of distilled water. Measured aqueous extract data have to be re-interpreted in order to infer porewater chemical composition of the sample because porewater chemistry changes significantly due to dilution and chemical reactions which take place during extraction. Here we present an inverse hydrochemical model to estimate porewater chemical composition from measured water content, aqueous extract, and mineralogical data. The model accounts for acid-base, redox, aqueous complexation, mineral dissolution/precipitation, gas dissolution/ex-solution, cation exchange and surface complexation reactions, of which are assumed to take place at local equilibrium. It has been solved with INVERSE-CORE{sup 2D} and been tested with bentonite samples taken from FEBEX (Full-scale Engineered Barrier EXperiment) in situ test. The inverse model reproduces most of the measured aqueous data except bicarbonate and provides an effective, flexible and comprehensive method to estimate porewater chemical composition of clays. Main uncertainties are related to kinetic calcite dissolution and variations in CO2(g) pressure.

Microwave Assisted Organic Synthesis of Heterocycles in Aqueous Media: Recent Advances in Medicinal Chemistry.

Science.gov (United States)

Frecentese, Francesco; Saccone, Irene; Caliendo, Giuseppe; Corvino, Angela; Fiorino, Ferdinando; Magli, Elisa; Perissutti, Elisa; Severino, Beatrice; Santagada, Vincenzo

2016-01-01

Green chemistry is a discipline of great interest in medicinal chemistry. It involves all fields of chemistry and it is based on the principle to conduct chemical reactions protecting the environment at the same time, through the use of chemical procedures able to avoid pollution. In this context, water as solvent is a good choice because it is abundant, nontoxic, non-caustic, and non-combustible. Even if microwave assisted organic reactions in conventional solvents have quickly progressed, in the recent years medicinal chemists have focused their attention to processes deemed not dangerous for the environment, using nanotechnology and greener solvents as water. Several reports of reaction optimizations and selectivities, demonstrating the capability of microwave to allow the obtaining of increased yields have been recently published using water as solvent. In this review, we selected the available knowledge related to microwave assisted organic synthesis in aqueous medium, furnishing examples of the newest strategies to obtain useful scaffolds and novel derivatives for medicinal chemistry purposes. The intention of this review is to demonstrate the exclusive ability of MAOS in water as solvent or as co-solvent. For this purpose we report here the most representative applications of MAOS using water as solvent, focusing on medicinal chemistry processes leading to interesting nitrogen containing heterocycles with potential pharmaceutical applications.

The activation of aluminium by mercury ions in non-aggressive media

Energy Technology Data Exchange (ETDEWEB)

Bessone, J.B. [INIEC-Dto de Ingenieria Quimica, Universidad Nacional del Sur, Av. Alem 1253, 8000 Bahia Blanca (Argentina)]. E-mail: jbessone@criba.edu.ar

2006-12-15

The presence of Hg at concentration less than 300 ppm in Al base alloys causes their passivation breakdown. On alloys used as sacrificial anodes, it causes a major lowering (>0.3 V) in their operational potential in chloride media. Mercury as trace constituent in the natural gas stream causes severe damage to cryogenic heat exchangers. The present paper presents evidences of the mechanism by which mercury produces its pronounced effect in aqueous non-aggressive media. The work was carried out using pure (99.99%) aluminium and mercury (II) acetate solutions of different concentrations and pH. Open circuit potential-time responses were obtained. The surface effects were followed by means of scanning microscopy and EDAX/X-Ray analysis. The results demonstrate that immediately after immersion, the initial air-formed oxide film underwent a dynamic crack-healing process at flaws in the film, possible associated to grain boundaries. The subsequent healing process, if any, depends on the media composition. Thus, in this special case, Hg{sup 2+} ions can be directly reduced on the bare aluminium, reaching a true metallic contact, and initiating surface diffusion. This enables the formation of an amalgam. Aluminium atoms diffuse through the liquid mercury and undergo oxidation at the amalgam/electrolyte interface. This process is responsible for the oxide detachment (by undermining) and the attack morphology (i.e., wide cavities). The presence of aggressive anions is not needed to initiate activation.

Dinitrosyl iron complexes with natural thiol-containing ligands in aqueous solutions: Synthesis and some physico-chemical characteristics (A methodological review).

Science.gov (United States)

Vanin, Anatoly F; Borodulin, Rostislav R; Mikoyan, Vasak D

2017-06-01

Two approaches to the synthesis of dinitrosyl iron complexes (DNIC) with glutathione and l-cysteine in aqueous solutions based on the use of gaseous NO and appropriate S-nitrosothiols, viz., S-nitrosoglutathione (GS-NO) or S-nitrosocysteine (Cys-NO), respectively, are considered. A schematic representation of a vacuum unit for generation and accumulation of gaseous NO purified from the NO 2 admixture and its application for obtaining aqueous solutions of DNIC in a Thunberg apparatus is given. To achieve this, a solution of bivalent iron in distilled water is loaded into the upper chamber of the Thunberg apparatus, while the thiol solution in an appropriate buffer (рН 7.4) is loaded into its lower chamber. Further steps, which include degassing, addition of gaseous NO, shaking of both solutions and formation of the Fe 2+ -thiol mixture, culminate in the synthesis of DNIC. The second approach consists in a stepwise addition of Fe 2+ salts and nitrite to aqueous solutions of glutathione or cysteine. In the presence of Fe 2+ and after the increase in рН to the physiological level, GS-NO or Cys-NO generated at acid media (pH nitrosonium ions (NO + ) and the peculiar characteristics of the EPR signal of their mononuclear form (M-DNIC). Copyright © 2017. Published by Elsevier Inc.

Hydrolysis of R7T7 nuclear waste glass in dilute media: mechanisms and rate as a function of pH

International Nuclear Information System (INIS)

Advocat, T.; Vernaz, E.; Charpentier, H.; Crovisier, J.L.; Ehret, G.

1990-01-01

R7T7 nuclear waste glass dissolution in highly dilute aqueous media under static conditions at 90 0 C occurs according to two different mechanisms depending on the solution acidity. In acid media (pH 4.8 and 5.5), preferential extraction of glass network modifiers results in the formation of an alkali metal-depleted surface region on which amorphous and crystallized (phosphate) compounds rich in transition elements precipitate. Steady-state dissolution conditions are not reached, as attested by variable normalized Si, B and Na mass losses. Glass dissolution is stoichiometric in basic media (pH 7 to 10): the strong bonds of the silicated network are broken at a rate that increases with the pH: the glass dissolution rate increases by a factor of 15 between pH 7 and 10. Under these conditions, alteration products at the glass/solution interface do not constitute a short-term kinetic barrier against the release of the major glass components

Studying the electrochemical deposition process of molybdenum from aqueous solution of molybdate ions

Directory of Open Access Journals (Sweden)

Samira Fikret Cafarova

2016-02-01

Full Text Available In this study, the tracing of the electroreduction process of molybdate ions in aqueous media at different conditions is achieved for obtaining molybdenum metal in a simple and easy way. The kinetics and the mechanism of the electroreduction of molybdate ions are studied using cathodic polarization technique. It is observed that, the speed of the electroreduction process depends on the speed of the change of the cathodic potential sweep as well as on the temperature of the electrodeposition bath. Moreover, it is observed that, at the potential range from the stationary potential (Est = 0.25V to −0.7 V, the electroreduction of molybdate ions occurs into two steps. Moreover it is observed that, after −0.7 V the electroreduction process of molybdate is accompanying with evolution of hydrogen.

Products of aqueous vitamin B5 (pantothenic acid) formed by free radical reactions

International Nuclear Information System (INIS)

Schittl, H.; Quint, R.M.; Getoff, N.

2007-01-01

The radiolysis of aqueous vitamin B5 (pantothenic acid) has been investigated under various experimental conditions. The highest vitamin degradation (G=3.22) was observed in solutions saturated with N 2 O, where 90% OH radicals are operating. As final products, the following were established: aldehydes, carboxylic acids and ammonia. Their yield strongly depends on the presence/absence of air as well as on N 2 O (used to convert e aq - into OH) and was determined as a function of absorbed radiation dose. HPLC-analysis showed that in all media, a main product is formed, having the highest yield in aerated solutions. Based on the chemical analysis, it appears that the OH radicals are most involved in the degradation process. A precise sequence of the reaction steps could not be given presently, because of the implication of many simultaneous reactions

Media Framing

DEFF Research Database (Denmark)

Pedersen, Rasmus T.

2017-01-01

The concept of media framing refers to the way in which the news media organize and provide meaning to a news story by emphasizing some parts of reality and disregarding other parts. These patterns of emphasis and exclusion in news coverage create frames that can have considerable effects on news...... consumers’ perceptions and attitudes regarding the given issue or event. This entry briefly elaborates on the concept of media framing, presents key types of media frames, and introduces the research on media framing effects....

Thermodynamic properties of aqueous solutions with citrate ions. Compressibility studies in aqueous solutions of citric acid

International Nuclear Information System (INIS)

Apelblat, Alexander; Korin, Eli; Manzurola, Emanuel

2013-01-01

Highlights: • Over a wide range of concentrations and temperatures sound velocities were measured in aqueous solutions of citric acid. • Compressibility properties of citric acid solutions are thermodynamically characterized. • Changes in the structure of water when citric acid is dissolved are discussed. -- Abstract: Sound velocities in aqueous solutions of citric acid were measured from 15 °C to 50 °C in 5 °C intervals, within the 0.1 mol · kg −1 to 5.0 mol · kg −1 concentration range. These sound velocities served to evaluate the isentropic and isothermal compressibilities, the apparent molar compressibilities, the isochoric thermal pressure coefficients, changes of the cubic expansion coefficients with pressure at constant temperature, the changes of heat capacities with volume and hydration numbers of citric acid in aqueous solutions

f-Element Ion Chelation in Highly Basic Media - Final Report

International Nuclear Information System (INIS)

Paine, R.T.

2000-01-01

A large body of data has been collected over the last fifty years on the chemical behavior of f-element ions. The ions undergo rapid hydrolysis reactions in neutral or basic aqueous solutions that produce poorly understood oxide-hydroxide species; therefore, most of the fundamental f-element solution chemistry has allowed synthetic and separations chemists to rationally design advanced organic chelating ligands useful for highly selective partitioning and separation of f-element ions from complex acidic solution matrices. These ligands and new examples under development allow for the safe use and treatment of solutions containing highly radioactive species. This DOE/EMSP project was undertaken to address the following fundamental objectives: (1) study the chemical speciation of Sr and lanthanide (Ln) ions in basic aqueous media containing classical counter anions found in waste matrices; (2) prepare pyridine N-oxide phosphonates and phosphonic acids that might act as selective chelator s for Ln ions in model basic pH waste streams; (3) study the binding of the new chelators toward Ln ions and (4) examine the utility of the chelators as decontamination and dissolution agents under basic solution conditions. The project has been successful in attacking selected aspects of the very difficult problems associated with basic pH solution f-element waste chemistry. In particular, the project has (1) shed additional light on the initial stages of Ln ion sol-gel-precipitate formulation under basic solution conditions; (2) generated new families of pyridine phosphonic acid chelators; (3) characterized the function of the chelators and (4) examined their utility as oxide-hydroxide dissolution agents. These findings have contributed significantly to an improved understanding of the behavior of Ln ions in basic media containing anions found in typical waste sludges as well as to the development of sludge dissolution agents. The new chelating reagents are easily made and could be

[Comparison of iodinated and barium-containing contrast media of different viscosity in the detection of pharyngeal perforation].

Science.gov (United States)

Keberle, M; Wittenberg, G; Trusen, A; Baumgartner, W; Hahn, D

2001-08-01

In contrast to esophageal perforations, the more radiopaque barium-suspensions are not as important as iodinated aqueous contrast agents for the detection of pharyngeal perforations. This study was performed to find out whether the highly different viscosities (of iodinated and barium-containing contrast agents with comparable radiopacities) are a reason for this. Viscosity, subjective difference in contrast, and CT-density of an iodinated aqueous (Telebrix) and a 50 wt/vol% barium-containing contrast agent (Micropaque) were determined. Moreover, to exclude postoperative perforation, 104 patients were prospectively examined by pharyngography using both contrast media. Pharyngographies of patients with perforation were later compared by two independent readers. All patients with perforation were followed up clinically to exclude complications due to barium administration. In-vitro comparison showed comparable radiopacity but the 50 wt/vol% barium-suspension was much more viscous than the iodinated contrast agent. During pharyngography, totally, 14 perforations were clearly delineated with the iodinated aqueous contrast agent. However, two of them were not detected with the barium-suspension. All the other perforations presented equally. Given a sufficient radiopacity, a low viscosity appears to be essential for a contrast agent to detect especially pharyngeal perforations. Thus, we recommend the sole use of an iodinated contrast agent (at suspicion of aspiration as isoosmolar variant) for this purpose.

Bioreactor droplets from liposome-stabilized all-aqueous emulsions

Science.gov (United States)

Dewey, Daniel C.; Strulson, Christopher A.; Cacace, David N.; Bevilacqua, Philip C.; Keating, Christine D.

2014-08-01

Artificial bioreactors are desirable for in vitro biochemical studies and as protocells. A key challenge is maintaining a favourable internal environment while allowing substrate entry and product departure. We show that semipermeable, size-controlled bioreactors with aqueous, macromolecularly crowded interiors can be assembled by liposome stabilization of an all-aqueous emulsion. Dextran-rich aqueous droplets are dispersed in a continuous polyethylene glycol (PEG)-rich aqueous phase, with coalescence inhibited by adsorbed ~130-nm diameter liposomes. Fluorescence recovery after photobleaching and dynamic light scattering data indicate that the liposomes, which are PEGylated and negatively charged, remain intact at the interface for extended time. Inter-droplet repulsion provides electrostatic stabilization of the emulsion, with droplet coalescence prevented even for submonolayer interfacial coatings. RNA and DNA can enter and exit aqueous droplets by diffusion, with final concentrations dictated by partitioning. The capacity to serve as microscale bioreactors is established by demonstrating a ribozyme cleavage reaction within the liposome-coated droplets.

Media Entrepreneurship

DEFF Research Database (Denmark)

Khajeheian, Datis

2017-01-01

Media Entrepreneurship has been an ambiguous, unclear and controversial concept and despite of growing academic efforts in the last decade, it is still a poorly defined subject. This paper is an effort to fill this gap by providing a comprehensive definition of media entrepreneurship. Firstly......, a literature review conducted and entrepreneurship, media, opportunity and innovation as building blocks of media entrepreneurship explained. Then by using of a mixed of bibliographic method and a Delphi method with multi-stage analysis process, a consensual definition of media entrepreneurship proposed...... entrepreneurship....

New media technologies and mass media reform processes

Directory of Open Access Journals (Sweden)

Tomić Boban

2017-01-01

Full Text Available This paper reviews and assesses the chances for survival and development of the media in Serbia and ib the region, from the perspective of new information and communication technologies (ICT applied in media business. In the paper theoretical method is used and harmonized with the needs of describing the problems and the observed processes and phenomena, as well as empirical method which is used for collecting and interpreting concrete facts and data on the observed processes and phenomena. The starting point lies in the fact that modern media is definitely, more and more, dependent on new technologies. A part of the new technologies is used in the process of collecting, selecting and editing media content, while the other part of the technology is used in the process of dissemination and propulsion of media content to the mass audience, and also in the feedback function as well. The technology revolution, which we describe, started with mp3, jpg and avi files, and continues with internet broadcasting, social networks, cloud technologies and new digital platforms which are used by today's media for distribution of media content. The particularity of the media in the region lies in the fact that they operating in the societes with delay of political and economic transition, so all the productive resources of society, due to this backlog, are slower adapted to the new conditions of business in the digital era. The consequences that have arisen from such dynamics of development make many media in Serbia and the region quite dysfunctional, especially those who were exposed during this transition to long-standing legal, economic and program crises. That is why most of the existing media in Serbia, especially small ones, are unprepared for modernization and they are not ready for re-modeling in accordance with the new technological circumstances.

Aqueous shunt implantation in glaucoma

Directory of Open Access Journals (Sweden)

Jing Wang

2017-01-01

Full Text Available Aqueous shunts or glaucoma drainage devices are increasingly utilized in the management of refractory glaucoma. The general design of the most commonly-used shunts is based on the principles of the Molteno implant: ie. a permanent sclerostomy (tube, a predetermined bleb area (plate and diversion of aqueous humour to the equatorial region and away from the limbal subconjunctival space. These three factors make aqueous shunts more resistant to scarring as compared to trabeculectomy. The two most commonly used shunts are the Ahmed Glaucoma Valve, which contains a flow-restrictor, and the non-valved Baervedlt Glaucoma Implant. While the valved implants have a lower tendency to hypotony and related complications, the non-valved implants with larger, more-biocompatible end plate design, achieve lower intraocular pressures with less encapsulation. Non-valved implants require additional suturing techniques to prevent early hypotony and a number of these methods will be described. Although serious shunt-related infection is rare, corneal decompensation and diplopia are small but significant risks.

Fixed bed column study for Cu (II) removal from aqueous solution using water hyacinth (Eichornia crassipes) biomass.

Science.gov (United States)

Gandhimathi, R; Ramesh, S T; Yadu, Anubhav; Bharathi, K S

2013-07-01

This paper reports the results of the study on the performance of low-cost biosorbent water hyacinth (WH) in removing Cu (II) from aqueous solution. The adsorbent material adopted was found to be an efficient media for the removal of Cu (II) in continuous mode using fixed bed column. The column studies were conducted with 10 mg/L metal solution with a flow rate of 10 mL/min with different bed depths such as 10, 20 and 30 cm. The column design parameters like adsorption rate constant, adsorption capacity and minimum bed depth were calculated. It was found that, the adsorption capacity of copper ions by water hyacinth increased by increasing the bed depth and the contact time.

[Media for 21st century--towards human communication media].

Science.gov (United States)

Harashima, H

2000-05-01

Today, with the approach of the 21st century, attention is focused on multi-media communications combining computer, visual and audio technologies. This article discusses the communication media target and the technological problems constituting the nucleus of multi-media. The communication media is becoming an environment from which no one can escape. Since the media has such a great power, what is needed now is not to predict the future technologies, but to estimate the future world and take to responsibility for future environments.

Media Ecology

Directory of Open Access Journals (Sweden)

Marina Ašković

2015-05-01

Full Text Available Does the trend in which electronic media are gradually becoming extension of human body have to move towards full enslavement of a human and his personality, or the same human will unpredictably, with the aid of his personal media literacy, exit the whirls of media and technological censorships? Personality crisis is closely related to the crisis of language no matter how contradicted to global ideology of transnational transhumanism it may seem. Considering the fact that recent media presentations of the world are based on commercialization of environmentalism, philosophical and aesthetic thought appears as an important subject of ecology. As media mediates, the scenery of civilized living increasingly becomes more appealing even though it derives from commercial and political background. Consequently, the future of humanity depends by large on the philosophy of media. Media have to truly ecologise returning the humanum to its essence making it into the extension of the natural world.

Media Education and Media Criticism in the Educational Process in Russia

Science.gov (United States)

Fedorov, Alexander; Levitskaya, Anastasia

2017-01-01

Media criticism and media education have a lot in common. For example, both media education and media criticism attach great importance to the development of analytical thinking of the audience. Indeed, one of the most important tasks of media education is precisely to teach the audience not only to analyze media texts of any types, but also to…

21 CFR 524.1200b - Kanamycin ophthalmic aqueous solution.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Kanamycin ophthalmic aqueous solution. 524.1200b... (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS OPHTHALMIC AND TOPICAL DOSAGE FORM NEW ANIMAL DRUGS § 524.1200b Kanamycin ophthalmic aqueous solution. (a) Specifications. The drug, which is in an aqueous...

Geographic Media Literacy

Science.gov (United States)

Lukinbeal, Chris

2014-01-01

While the use of media permeates geographic research and pedagogic practice, the underlying literacies that link geography and media remain uncharted. This article argues that geographic media literacy incorporates visual literacy, information technology literacy, information literacy, and media literacy. Geographic media literacy is the ability…

SOCIAL MEDIA SECURITY

Science.gov (United States)

RESPONSIBILITY CENTCOM COALITION MEDIA SOCIAL MEDIA NEWS ARTICLES PRESS RELEASES IMAGERY VIDEOS TRANSCRIPTS VISITORS AND PERSONNEL FAMILY CENTER FAMILY READINESS CENTCOM WEBMAIL SOCIAL MEDIA SECURITY ACCOUNTABILITY HomeVISITORS AND PERSONNELSOCIAL MEDIA SECURITY FAQ on Security for Social Media Due to the widespread use of

Electrochemical reactions of uranyl(VI) complexes in aqueous solution, non-aqueous solvents, and ionic liquids

International Nuclear Information System (INIS)

Ikeda, Yasuhisa

2006-01-01

Author's recent experimental results on the chemistry of U(V) in aqueous solution, non-aqueous solvents, and ionic solvents by cyclic voltametry are described. The U(V) was produced by electrochemical reduction of uranyl U(VI) ions or complexes such as carbonates, DMF(N, N-dimethylformamide), DMSO(dimethylsulfoxide), acetylacetonato, and other organic polydental ligands. The produced U(V) complexes were studied by spectrophotometry using optical-transmission thin-layer electrode. The U(V) complexes in non-aqueous solvents were found to be rather stable, they undergo ligand-dissociation reaction but not disproportionation reaction. The structure and electronic spectra as well as IR spectra of the complexes were studied. The present method was further developed to study the behavior of U(V) complexes in ionic liquids as molten salts, e.g., alkaline metals chlorides. Thus, the present research contributes to understanding the chemistry of 5fl system. Application to such nuclear technology as spent fuel reprocessing is discussed. (S. Ohno)

Measurement of Interfacial Area Production and Permeability within Porous Media

International Nuclear Information System (INIS)

Crandall, Dustin; Ahmadi, Goodarz; Smith, Duane H.

2010-01-01

An understanding of the pore-level interactions that affect multi-phase flow in porous media is important in many subsurface engineering applications, including enhanced oil recovery, remediation of dense non-aqueous liquid contaminated sites, and geologic CO 2 sequestration. Standard models of two-phase flow in porous media have been shown to have several shortcomings, which might partially be overcome using a recently developed model based on thermodynamic principles that includes interfacial area as an additional parameter. A few static experimental studies have been previously performed, which allowed the determination of static parameters of the model, but no information exists concerning the interfacial area dynamic parameters. A new experimental porous flow cell that was constructed using stereolithography for two-phase gas-liquid flow studies was used in conjunction with an in-house analysis code to provide information on dynamic evolution of both fluid phases and gas-liquid interfaces. In this paper, we give a brief introduction to the new generalized model of two-phase flow model and describe how the stereolithography flow cell experimental setup was used to obtain the dynamic parameters for the interfacial area numerical model. In particular, the methods used to determine the interfacial area permeability and production terms are shown.

ANALISIS CATEGORY ADVERTISING EXPENDITURE DAN CONSUMER MEDIA HABIT DI MEDIA TELEVISI DAN MEDIA CETAK

Directory of Open Access Journals (Sweden)

Zifwen Zifwen

2011-08-01

Full Text Available Normal 0 false false false MicrosoftInternetExplorer4 The purpose of the study is to identify the category of advertising expenditure and media habit on media advertising, especially on television and print ad such as newspapers, magazines and tabloids. The Data were collected  from Nielsen Media Research (NMR data base from a number of cities in Indonesia, such as Jakarta,Surabaya, Bandung, Semarang, Surabaya, Yogyakarta, Bali, Medan,Palembang and Makassar. There are three different type of data used to acquire the secondary data for the study: (1  Telescope (data collected for rating analysis January 1st, 2005 to March 31st, 2005, (2 Print scope (data collected from the readership of magazines, tabloids and newspaper January 1st, 2004 to December 31st, 2004 and (3 Ad quest (data collected from advertising expenditure for all categories. The data were collected, calculated and analyzed from January 1st, 2002 to December 31st, 2004. The purpose of the study is to uncover the trend of advertising budget from all categories on the television and print ads, in order to describe the consumption tendency of the people within advertising media. Index analysis and Biplot were used to analyze the data. Based on the result of advertising expenditure analysis of data, showing that all categories were completely different in the utilization of the media for advertisement. Some categories used mix media to support their campaign and others used a single media. Characteristic of the categories were strongly involved in the decision making in way of choosing and using the advertising media. The result of consumer media analysis found that the people habit were completely different and unique in media consumption. Different of age, sex and social economic status can create a different habit in term of hobbies and desire within the channel, programme, newspaper, magazines and the tabloids. Finally, to create an effective and efficient advertising activity

Ion reactivity of calcium-deficient hydroxyapatite in standard cell culture media.

Science.gov (United States)

Gustavsson, J; Ginebra, M P; Engel, E; Planell, J

2011-12-01

Solution-mediated surface reactions occur for most calcium phosphate-based biomaterials and may influence cellular response. A reasonable extrapolation of such processes observed in vitro to in vivo performance requires a deep understanding of the underlying mechanisms. We therefore systematically investigated the nature of ion reactivity of calcium-deficient hydroxyapatite (CDHA) by exposing it for different periods of time to standard cell culture media of different chemical composition (DMEM and McCoy medium, with and without osteogenic supplements and serum proteins). Kinetic ion interaction studies of principal extracellular ions revealed non-linear sorption of Ca²⁺ (∼50% sorption) and K⁺ (∼8%) as well as acidification of all media during initial contact with CDHA (48h). Interestingly, inorganic phosphorus (P(i)) was sorbed from McCoy medium (∼50%) or when using osteogenic media containing β-glycerophosphate, but not from DMEM medium. Non-linear sorption data could be perfectly described by pseudo-first-order and pseudo-second-order sorption models. At longer contact time (21 days), and with frequent renewal of culture medium, sorption of Ca²⁺ remained constant throughout the experiment, while sorption of P(i) gradually decreased in McCoy medium. In great contrast, CDHA began to release P(i) slowly with time when using DMEM medium. Infrared spectra showed that CDHA exposed to culture media had a carbonated surface chemistry, suggesting that carbonate plays a key role in the ion reactivity of CDHA. Our data show that different compositions of the aqueous environment may provoke opposite ion reactivity of CDHA, and this must be carefully considered when evaluating the osteoinductive potential of the material. Copyright © 2011 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Stabilized aqueous gels and uses thereof

Energy Technology Data Exchange (ETDEWEB)

Swanson, B.L.

1978-08-29

New improved aqueous gels, and methods of using same in contacting subterranean formations, are provided. The gels are prepared by gelling an aqueous brine having incorporated therein a water-soluble cellulose ether such as a carboxymethylcellulose (CMC), and are rendered more stable to decomposition by incorporating a sulfoalkylated tannin stabilizing agent, such as a sulfomethylated quebracho (SMQ), in the gel during the preparation thereof.

Aqueous shunts for glaucoma.

Science.gov (United States)

Tseng, Victoria L; Coleman, Anne L; Chang, Melinda Y; Caprioli, Joseph

2017-07-28

Aqueous shunts are employed to control intraocular pressure (IOP) for people with primary or secondary glaucomas who fail or are not candidates for standard surgery. To assess the effectiveness and safety of aqueous shunts for reducing IOP in glaucoma compared with standard surgery, another type of aqueous shunt, or modification to the aqueous shunt procedure. We searched CENTRAL (which contains the Cochrane Eyes and Vision Trials Register) (2016, Issue 8), MEDLINE Ovid (1946 to August 2016), Embase.com (1947 to August 2016), PubMed (1948 to August 2016), LILACS (Latin American and Caribbean Health Sciences Literature Database) (1982 to August 2016), ClinicalTrials.gov (www.clinicaltrials.gov); searched 15 August 2016, and the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP) (www.who.int/ictrp/search/en); searched 15 August 2016. We did not use any date or language restrictions in the electronic search for trials. We last searched the electronic databases on 15 August 2016. We also searched the reference lists of identified trial reports and the Science Citation Index to find additional trials. We included randomized controlled trials that compared various types of aqueous shunts with standard surgery or to each other in eyes with glaucoma. Two review authors independently screened search results for eligibility, assessed the risk of bias, and extracted data from included trials. We contacted trial investigators when data were unclear or not reported. We graded the certainty of the evidence using the GRADE approach. We followed standard methods as recommended by Cochrane. We included 27 trials with a total of 2099 participants with mixed diagnoses and comparisons of interventions. Seventeen studies reported adequate methods of randomization, and seven reported adequate allocation concealment. Data collection and follow-up times varied.Four trials compared an aqueous shunt (Ahmed or Baerveldt) with trabeculectomy, of which

Efficient Isomerization of Glucose to Fructose over Zeolites in Consecutive Reactions in Alcohol and Aqueous Media

DEFF Research Database (Denmark)

Shunmugavel, Saravanamurugan; Paniagua, Marta; Melero, Juan A

2013-01-01

glucose isomerization to fructose and subsequent reaction with methanol to form methyl fructoside (step 1), followed by hydrolysis to re-form fructose after water addition (step 2). NMR analysis with (13)C-labeled sugars confirmed this reaction pathway. Conversion of glucose for 1 h at 120 °C with H......-USY (Si/Al = 6) gave a remarkable 55% yield of fructose after the second reaction step. A main advantage of applying alcohol media and a catalyst that combines Brønsted and Lewis acid sites is that glucose is isomerized to fructose at low temperatures, while direct conversion to industrially important...

Media Culture and Media Education in Modern School

Science.gov (United States)

Tolic, Mirela

2011-01-01

Culture is no longer conceivable without the media and/or new phenomena called. "Cyber" culture. The article discusses issues in what respect the different media, like TV, film and Internet are with different cultures, how it changes everyday life under influence of various forms of sophisticated communications media and what…

New technetium-99m generator technologies utilizing polyethylene glycol-based aqueous piphasic systems

International Nuclear Information System (INIS)

Rogers, R.D.; Bond, A.H.; Zhang, Jianhua

1995-01-01

Two new schemes for TcO 4 - /MoO 4 2- separations from OH - and MoO 4 2- media using polyethylene glycol (PEG)-based aqueous biphasic systems (ABS) have been developed. The two most important salt solutions in current 99m Tc-generator technologies, OH - and MoO 4 2- , also salt out PEG to form ABS. In liquid/liquid PEG- ABS, pertechnetate can be separated from molybdate with separation factors as high as 10,000. Stripping is accomplished by reduction of the TcO 4 - and back extraction into a salt solution. the strip solution can be the salt of an imaging agent (e.g., Na 4 HEDPA) and thus may, under the appropriate conditions, be injected directly into the human body. 99m TcO 4 - can also be concentrated from a dilute load solution of 99 MoO 4 2- in NaOH using an aqueous biphasic extraction chromatographic technique (ABEC). A rinse with K 2 CO 3 assures that all 99 MoO 4 2- is removed from the column and this is confirmed by a rapid drop in 99 Mo activity by the fourth free column volume (fcv) of rinse. The 99m TcO 4 - is then eluted with water. This chromatographic separation affords 94% of the 99m TcO 4 - activity in 5 fcv, with the y spectrum showing less than 2 x 10 -4 of the original 99 Mo activity

Fluorescence excitation-emission matrix (EEM) spectroscopy for rapid identification and quality evaluation of cell culture media components.

Science.gov (United States)

Li, Boyan; Ryan, Paul W; Shanahan, Michael; Leister, Kirk J; Ryder, Alan G

2011-11-01

The application of fluorescence excitation-emission matrix (EEM) spectroscopy to the quantitative analysis of complex, aqueous solutions of cell culture media components was investigated. These components, yeastolate, phytone, recombinant human insulin, eRDF basal medium, and four different chemically defined (CD) media, are used for the formulation of basal and feed media employed in the production of recombinant proteins using a Chinese Hamster Ovary (CHO) cell based process. The comprehensive analysis (either identification or quality assessment) of these materials using chromatographic methods is time consuming and expensive and is not suitable for high-throughput quality control. The use of EEM in conjunction with multiway chemometric methods provided a rapid, nondestructive analytical method suitable for the screening of large numbers of samples. Here we used multiway robust principal component analysis (MROBPCA) in conjunction with n-way partial least squares discriminant analysis (NPLS-DA) to develop a robust routine for both the identification and quality evaluation of these important cell culture materials. These methods are applicable to a wide range of complex mixtures because they do not rely on any predetermined compositional or property information, thus making them potentially very useful for sample handling, tracking, and quality assessment in biopharmaceutical industries.

Post Media Literacy: Menyaksikan Kuasa Media Bersama Michel Foucault

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Iswandi Syahputra

2017-01-01

Full Text Available This article would like to present Michel Foucault’s idea concerning Knowledge and Power in media industry. As a contemporary intellectual, Foucault’s thought has a unique style of postmodernism. His thought had gone beyond traditional critical theory whose trying to disclose the relation of power and economic behind the ideology of media. Foucault’s thought had given new perspective in understanding how the media produce truth under tightly control process into something that seems normal. With the assumption of media has the power to create mass culture, which has to be studied critically by media literacy approach, Foucault’s thought had given new space of discursive. An alternative thought on how to estimate the work of mass media as supervisor of truth and creator of information trough normalization practice.

Locative media

CERN Document Server

Wilken, Rowan

2014-01-01

Not only is locative media one of the fastest growing areas in digital technology, but questions of location and location-awareness are increasingly central to our contemporary engagements with online and mobile media, and indeed media and culture generally. This volume is a comprehensive account of the various location-based technologies, services, applications, and cultures, as media, with an aim to identify, inventory, explore, and critique their cultural, economic, political, social, and policy dimensions internationally. In particular, the collection is organized around the perception that the growth of locative media gives rise to a number of crucial questions concerning the areas of culture, economy, and policy.

Radiation response of vitamin A in aqueous dispersions

International Nuclear Information System (INIS)

Bhushan, B.; Kumta, U.S.

1977-01-01

The radiation destruction of vitamin A acetate was monitored in isooctane, coconut oil, and aqueous dispersions. The G(-vit. A), i.e., the number of vitamin A molecules destroyed per 100 eV of energy absorbed in lipid solvents and aqueous preparations, increased with the concentrations of vitamin A used. In the freely dissolved state, as in isooctane or coconut oil, the extent of destruction of vitamin A was more or less identical. However, a marked reduction in the radiation destruction of vitamin A was observed in aqueous dispersions at all concentrations except at 1 x 10 -4 M. Incorporation of sugars, starch, and egg albumin in aqueous preparations offered considerable protection to vitamin A from radiation damage which could be discerned even at the lowest concentration (1 x 10 -4 M). The protective influence of aqueous dispersion as noted for vitamin A was also observed for β-carotene, vitamin A alcohol, and ubiquinone-30. The significance of the above findings in radiation processing of foods has been discussed

Expression of cytokines in aqueous humor from fungal keratitis patients.

Science.gov (United States)

Zhang, Yingnan; Liang, Qingfeng; Liu, Yang; Pan, Zhiqiang; Baudouin, Christophe; Labbé, Antoine; Lu, Qingxian

2018-04-19

Although a series of reports on corneal fungal infection have been published, studies on pathogenic mechanisms and inflammation-associated cytokines remain limited. In this study, aqueous humor samples from fungal keratitis patients were collected to examine cytokine patterns and cellular profile for the pathogenesis of fungal keratitis. The aqueous humor samples were collected from ten patients with advanced stage fungal keratitis. Eight aqueous humor samples from patients with keratoconus or corneal dystrophy were taken as control. Approximately 100 μl to 300 μl of aqueous humor in each case were obtained for examination. The aqueous humor samples were centrifuged and the cells were stained and examined under optical microscope. Bacterial and fungal cultures were performed on the aqueous humor and corneal buttons of all patients. Cytokines related to inflammation including IL-1β, IL-6, IL-8, IL-10, TNF-α, and IFN-γ were examined using multiplex bead-based Luminex liquid protein array systems. Fungus infection was confirmed in these ten patients by smear stains and/or fungal cultures. Bacterial and fungal cultures revealed negative results in all aqueous humor specimens. Polymorphonuclear leukocytes were the predominant infiltrating cells in the aqueous humor of fungal keratitis. At the advanced stages of fungal keratitis, the levels of IL-1β, IL-6, IL-8, and IFN-γ in the aqueous humor were significantly increased when compared with control (phumor was associated with fungal keratitis.

As (V) biosorption in an aqueous solution using chemically treated lemon (Citrus aurantifolia Swingle) residues.

Science.gov (United States)

Marín-Rangel, Vania Marilyn; Cortés-Martínez, Raúl; Villanueva, Ruth Alfaro Cuevas; Garnica-Romo, Ma Guadalupe; Martínez-Flores, Héctor Eduardo

2012-01-01

The use of biosorbents to remove metals and metalloids from contaminated water systems has gained great usage in various parts of the world. The objective of the current study was to test lemon peels as biosorbents for As (V). Lemon peels were chemically characterized and arsenic contact experiments were performed to determine the adsorption capacity of the peels using different empirical models. The model that fit the experimental data was the Lagergren empirical model with a correlation coefficient of R= 0.8841. The results show that lemon peels were able to retain 474.8 μg of As (V)/g of biosorbent. Lemon agro-industrial waste can be useful in the removal of heavy metals, such as arsenic, from aqueous media. © 2011 Institute of Food Technologists®

Hydrogen Bonded Supramolecular Polymers in Both Apolar and Aqueous Media： Self-Assembly and Reversible Conversion of Vesicles and Gels%Hydrogen Bonded Supramolecular Polymers in Both Apolar and Aqueous Media： Self-Assembly and Reversible Conversion of Vesicles and Gels

Institute of Scientific and Technical Information of China (English)

杜平; 孔军; 王贵涛; 赵新; 李光玉; 蒋锡夔; 黎占亭

2011-01-01

In a preliminary letter （Tetrahedron Lett. 2010, 51, 188）, we reported two new hydrazide-based quadruple hydrogen-bonding motifs, this is, two monopodal （la and lb） and five dipodal （2a, 2b and 3a--3c） aromatic hydrazide derivatives, and the formation of supramolecular polymers and vesicles from the dipodal motifs in hydrocarbons. In this paper, we present a full picture on the properties of these hydrogen-bonding motifs with an emphasis on their self-assembling behaviors in aqueous media. SEM, AFM, TEM and fluorescent micrographs indicate that all the dipodal compounds also form vesicles in polar methanol and water-methanol （up to 50% of water） mixtures. Control experiments show that lb does not form vesicles in same media. Addition of lb to the solution of the dipodal compounds inhibits the latter＇s capacity of forming vesicles. At high concentrations, 3b and 3c also gelate discrete solvents, including hydrocarbons, esters, methanol, and methanol-water mixture. Concentration-dependent SEM investigations reveal that the vesicles of 3b and 3c fuse to form gels and the gel of 3c can de-aggregate to form the vesicles reversibly.

On Media Education

Science.gov (United States)

Fedorov, Alexander

2008-01-01

This monograph analyzes the theory and practice of media education and media literacy. The book also includes the list of Russian media education literature and addresses of websites of the associations for media education.

More Media, More People—On Social & Multimodal Media Intelligence

OpenAIRE

Degerstedt, Lars; Pelle, Snickars

2017-01-01

The purpose of this article is to address some challenges facing media intelligence in general, and competitive intelligence in particular within an altered information landscape. To understand this new situation, the notion of social and multimodal media intelligence are introduced. With cases taken primarily from the Swedish media intelligence sector, we argue that data driven media intelligence today needs to pay increasing attention to new forms of (A.) crowd-oriented and (B.) multimedia-...

Products of aqueous vitamin B5 (pantothenic acid) formed by free radical reactions

Energy Technology Data Exchange (ETDEWEB)

Schittl, H. [Section of Radiation Biology, Department of Nutritional Sciences, University of Vienna, Althanstr. 14, UZA II, A-1090 Vienna (Austria); Quint, R.M. [Section of Radiation Biology, Department of Nutritional Sciences, University of Vienna, Althanstr. 14, UZA II, A-1090 Vienna (Austria); Getoff, N. [Section of Radiation Biology, Department of Nutritional Sciences, University of Vienna, Althanstr. 14, UZA II, A-1090 Vienna (Austria)]. E-mail: nikola.getoff@univie.ac.at

2007-10-15

The radiolysis of aqueous vitamin B5 (pantothenic acid) has been investigated under various experimental conditions. The highest vitamin degradation (G=3.22) was observed in solutions saturated with N{sub 2}O, where 90% OH radicals are operating. As final products, the following were established: aldehydes, carboxylic acids and ammonia. Their yield strongly depends on the presence/absence of air as well as on N{sub 2}O (used to convert e{sub aq} {sup -} into OH) and was determined as a function of absorbed radiation dose. HPLC-analysis showed that in all media, a main product is formed, having the highest yield in aerated solutions. Based on the chemical analysis, it appears that the OH radicals are most involved in the degradation process. A precise sequence of the reaction steps could not be given presently, because of the implication of many simultaneous reactions.

f-Element Ion Chelation in Highly Basic Media

International Nuclear Information System (INIS)

Paine, Robert T.

1999-01-01

High-level radioactive waste (HLW) generated in the DOE complex is stored in tanks at several sites, but predominantly it is found at the Hanford reservation. Much of the material has been exposed to high pHs, consequently the waste exists in a complex, poorly understood mixture of solids, gels and solutions. The final waste remediation plan may involve chemical separation of fractions and a suitable, well developed molecular chemistry basis for performing these separations is not available. Indeed, the fundamental chemical behavior of most radioactive nuclides in basic media is not known. The goal of this project is to undertake fundamental studies of the coordination chemistry of f-element species in basic aqueous solutions containing common waste treatment ions (e.g., NO3 -, CO3 2-, organic carboxylates, and EDTA), as well as new waste scrubbing chelators produced in this study. The experimental agenda includes: 1. Studies of the speciation of Sr and Ln ions in basic solutions wit h and without common counterions; 2. Preparations of new multifunctional ligands that may act as strong, ion-specific chelators for Sr and/or Ln ions in basic media; and 3. Studies of the coordination and dissolution behavior of oxide-hydroxide species, as well as in insoluble sols, gels, and precipitates in combination with new chelating ligands. It is anticipated that this coordination chemistry will facilitate the design of advanced separation schemes required for handling the complex waste matrices found at the Hanford HLW facility

Application of E{sub h}-pH diagram for room temperature precipitation of zinc stannate microcubes in an aqueous media

Energy Technology Data Exchange (ETDEWEB)

Al-Hinai, Ashraf T., E-mail: ashraf@squ.edu.om [Department of Chemistry, College of Science, Sultan Qaboos University, 123, Alkhoud (Oman); Al-Hinai, Muna H. [Department of Chemistry, College of Science, Sultan Qaboos University, 123, Alkhoud (Oman); Water Research Center, Sultan Qaboos University, 123, Alkhoud (Oman); Dutta, Joydeep, E-mail: dutta@squ.ed.om [Water Research Center, Sultan Qaboos University, 123, Alkhoud (Oman)

2014-01-01

Graphical abstract: - Highlights: • One pot aqueous synthesis of zinc stannate (ZnSnO{sub 3}) particles at low temperature. • Synthesis designed with the assistance of potential-pH diagram. • ZnSnO{sub 3} estimated to be stable between pH 8 and 12 was used for synthesis of the particles. • ZnSnO{sub 3}·3H{sub 2}O were formed during the precipitation of zinc stannate. - Abstract: Potential-pH diagram assisted-design for controlled precipitation is an attractive method to obtain engineered binary and ternary oxide particles. Aqueous synthesis conditions of zinc stannate (ZnSnO{sub 3}) particles at low temperature were formulated with the assistance of potential-pH diagram. The pH of a solution containing stoichiometric amounts of Zn{sup 2+} and Sn{sup 4+} was controlled for the precipitation in a one pot synthesis step at room temperature (25 °C). The effect of the concentration of the reactants on the particle size was studied by varying the concentration of the precursor (Zn{sup 2+} + Sn{sup 4+}) solution. Scanning electron micrographs show that the particles are monodispersed micron sized cubes formed by the self-organization of nano-sized crystallites. The obtained microcubes characterized by X-ray Diffraction and thermo gravimetric analysis (TGA) show that the particles are in ZnSnO{sub 3}·3H{sub 2}O form.

Novel Schiff base (DBDDP) selective detection of Fe (III): Dispersed in aqueous solution and encapsulated in silica cross-linked micellar nanoparticles in living cell.

Science.gov (United States)

Gai, Fangyuan; Yin, Li; Fan, Mengmeng; Li, Ling; Grahn, Johnny; Ao, Yuhui; Yang, Xudong; Wu, Xuming; Liu, Yunling; Huo, Qisheng

2018-03-15

This work demonstrated the synthesis of (4E)-4-(4-(diphenylamino)benzylideneamino)-1,2-dihydro-1,5- dimethyl-2-phenylpyrazol-3-one (DBDDP) for Fe (III) detection in aqueous media and in the core of silica cross-linked micellar nanoparticles in living cells. The free DBDDP performed fluorescence enhancement due to Fe (III)-promoted hydrolysis in a mixed aqueous solution, while the DBDDP-doped silica cross-linked micellar nanoparticles (DBDDP-SCMNPs) performed an electron-transfer based fluorescence quenching of Fe (III) in living cells. The quenching fluorescence of DBDDP-SCMNPs and the concentration of Fe (III) exhibited a linear correlation, which was in accordance with the Stern-Volmer equation. Moreover, DBDDP-SCMNPs showed a low limit of detection (LOD) of 0.1 ppm and an excellent selectivity against other metal ions. Due to the good solubility and biocompatibility, DBDDP-SCMNPs could be applied as fluorescence quenching nanosensors in living cells. Copyright © 2017 Elsevier Inc. All rights reserved.

Modeling seismic stimulation: Enhanced non-aqueous fluid extraction from saturated porous media under pore-pressure pulsing at low frequencies

Science.gov (United States)

Lo, Wei-Cheng; Sposito, Garrison; Huang, Yu-Han

2012-03-01

Seismic stimulation, the application of low-frequency stress-pulsing to the boundary of a porous medium containing water and a non-aqueous fluid to enhance the removal of the latter, shows great promise for both contaminated groundwater remediation and enhanced oil recovery, but theory to elucidate the underlying mechanisms lag significantly behind the progress achieved in experimental research. We address this conceptual lacuna by formulating a boundary-value problem to describe pore-pressure pulsing at seismic frequencies that is based on the continuum theory of poroelasticity for an elastic porous medium permeated by two immiscible fluids. An exact analytical solution is presented that is applied numerically using elasticity parameters and hydraulic data relevant to recent proof-of-principle laboratory experiments investigating the stimulation-induced mobilization of trichloroethene (TCE) in water flowing through a compressed sand core. The numerical results indicated that significant stimulation-induced increases of the TCE concentration in effluent can be expected from pore-pressure pulsing in the frequency range of 25-100 Hz, which is in good agreement with what was observed in the laboratory experiments. Sensitivity analysis of our numerical results revealed that the TCE concentration in the effluent increases with the porous medium framework compressibility and the pulsing pressure. Increasing compressibility also leads to an optimal stimulation response at lower frequencies, whereas changing the pulsing pressure does not affect the optimal stimulation frequency. Within the context of our model, the dominant physical cause for enhancement of non-aqueous fluid mobility by seismic stimulation is the dilatory motion of the porous medium in which the solid and fluid phases undergo opposite displacements, resulting in stress-induced changes of the pore volume.

PENGEMBANGAN MEDIA PEMBELAJARAN FILM ANIMASI SEBAGAI MEDIA PEMBELAJARAN KONSEP FOTOSINTESIS

Directory of Open Access Journals (Sweden)

Umrotul Hasanah

2015-11-01

Full Text Available The research aims to develop animation film as a learning media in photosynthesis concept learning and to know the results of the assessment of the learning media expert test the concept of photosynthesis animated films. This research is Research and Development (R&D. The research used questionnaire  Aspects of assessment in terms of the media covering aspects of technical quality, narration, and music/sound effects. Aspects of the assessment of the suitability of the material terms covering the material aspects of the curriculum, the clarity of the material, the order of the material, communicative, suitability of the material with the purpose of learning, material relationship with the students’ critical thinking skill, and material relationship with motivation. Media expert test against “Cahaya dan Fotosintesis” animated film made by media experts with a percentage of 80,6% with the as good category, and  92,5% are material expert excellent category. Based on the “Cahaya dan Fotosintesis” animated film expert test to students can be tasted on a limited basis, after the media deficiencies corrected. Penelitian ini bertujuan untuk mengembangkan media pembelajaran film animasi pada konsep fotosintesis dan untuk mengetahui hasil penilaian uji ahli terhadap media pembelajaran film animasi pada konsep fotosintesis. Penelitian ini merupakan penelitian research and development (R & D. Teknik pengumpulan data dengan menggunakan angket. Aspek penilaian dari segi media meliputi aspek kualitas teknik, narasi dan musik/efek suara. Aspek penilaian dari segi materi meliputi aspek kesesuaian materi dengan kurikulum, kejelasan materi, urutan materi, komunikatif, kesesuaian soal evaluasi, kesesuaian materi dengan tujuan pembelajaran, hubungan materi dengan kemampuan berpikir kritis dan hubungan materi dengan motivasi. Uji ahli terhadap media film animasi “Cahaya dan Fotosintesis” dilakukan oleh ahli media dengan perolehan persentse 80,6% dengan

[Preoperatively administered flomoxef sodium concentration in aqueous humor].

Science.gov (United States)

Miyamoto, Mariko; Watanabe, Yoichiro; Mizuki, Nobuhisa

2007-04-01

We intravenously administered flomoxef sodium (FMOX) 0.5-3.5 hours before cataract surgery and measured the concentration of the agent in the aqueous humor to investigate its penetration into the aqueous humor and its efficacy in the prevention of postoperative endophthalmitis. 56 patients who underwent cataract surgery were enrolled in this study. They received 1 g FMOX via a 20-minute intravenous drip beginning 0.5-3.5 hours before the operation. Aqueous humor was aspirated from the anterior chamber and assayed for FMOX concentration using high-performance liquid chromatography. The mean intraoperative FMOX concentrations in the patients' aqueous humor were 0.79 +/- 0.24 microg/ml (administered 3.5 hours before surgery)--1.47 0.79 microg/ml (administered 1.5 hours before surgery). These concentrations administered 0.5-3.0 hours before surgery sufficiently exceeded the minimum inhibitory concentration (MIC) 90 values against Staphylococcus epidermidis, Staphylococcus aureus and Propionibacterium acnes, but did not achieve the MIC90 values against Enterococcus faecalis and Pseudomonas aeruginosa. The FMOX concentrations in the aqueous humor sampling were adequate to kill bacteria in vitro. This drug may be efficacious in the prevention of postoperative endophthalmitis in patients undergoing cataract surgery.

Social Media Reputation

DEFF Research Database (Denmark)

Etter, Michael Andreas; Ravasi, Davide; Colleoni, Elanor

motivational drivers and contextual conditions associated with the formation of narratives in traditional news media and social media influence their content, diffusion, and impact significantly. Our analysis suggests that current theories of media reputation may provide an incomplete representation......Social media enable millions of users to create and disseminate narratives about organizations that increase their public exposure and shape public perceptions. In this paper, we draw on the sociology of news production and research on computer-mediated communication to discuss how different...... of the phenomenon, and highlight theoretically relevant differences and interrelationships between reputational dynamics involving news media and social media....

AMAMM - All Media Are Mixed Media

DEFF Research Database (Denmark)

All Media Are Mixed Media Alle medier er blandingsmedier. Alle kunstarter er kompositte. Alle sanser er sammensatte. Alle medialiteter er miksede og mangfoldige. Alle er AMAMM. Denne påstand står centralt i ord-, billed- og medie-teoretikeren W.J.T. Mitchells forfatterskab. I hosstående bog tager...

Toxic effects and bioaccumulation of nano-, micron- and aqueous-Ag in the estuarine polychaete, Nereis (Hediste) diversicolor

DEFF Research Database (Denmark)

cong, Yi

concern about the fate and potential risks of nanosilver for the aquatic environment after its eventual release via wastewater discharges. In this thesis, dispersion and stability tests of commercially available nano (Ag particles in two media (deionized water vs....... filtered natural seawater) were firstly performed with the purpose to investigate the behavior of Ag particles in aqueous environments. A sediment exposure pathway was selected for the following toxicity experiments (I and II) as both Ag particles tended to precipitate in the water phase over time. Due...... to the importance of fully characterizing nanoparticles for interpretation of toxicity results, the crystal structure, particle size and morphology of commercial nano (Ag particles were determined in parallel to the toxicity studies. The characterization of hydrodynamic...

Phytochemical constituents and antioxidant activities of aqueous ...

African Journals Online (AJOL)

Furthermore, total phenolic content in aqueous extract (0.66 ± 0.02 mg gallic acid equivalent/g) was significantly higher (p < 0.05) than methanol extract (0.52 ± 0.01 mg gallic acid equivalent/g). In addition, inhibition of lipid peroxidation by aqueous extract (80.60 ± 0.28%) was significantly higher (p < 0.05) than methanol ...

pH-dependent solubility of indomethacin-saccharin and carbamazepine-saccharin cocrystals in aqueous media.

Science.gov (United States)

Alhalaweh, Amjad; Roy, Lilly; Rodríguez-Hornedo, Naír; Velaga, Sitaram P

2012-09-04

Cocrystals constitute an important class of pharmaceutical solids for their remarkable ability to modulate solubility and pH dependence of water insoluble drugs. Here we show how cocrystals of indomethacin-saccharin (IND-SAC) and carbamazepine-saccharin (CBZ-SAC) enhance solubility and impart a pH-sensitivity different from that of the drugs. IND-SAC exhibited solubilities 13 to 65 times higher than IND at pH values of 1 to 3, whereas CBZ-SAC exhibited a 2 to 10 times higher solubility than CBZ dihydrate. Cocrystal solubility dependence on pH predicted from mathematical models using cocrystal K(sp), and cocrystal component K(a) values, was in excellent agreement with experimental measurements. The cocrystal solubility increase relative to drug was predicted to reach a limiting value for a cocrystal with two acidic components. This limiting value is determined by the ionization constants of cocrystal components. Eutectic constants are shown to be meaningful indicators of cocrystal solubility and its pH dependence. The two contributions to solubility, cocrystal lattice and solvation, were evaluated by thermal and solubility determinations. The results show that solvation is the main barrier for the aqueous solubility of these drugs and their cocrystals, which are orders of magnitude higher than their lattice barriers. Cocrystal increase in solubility is thus a result of decreasing the solvation barrier compared to that of the drug. This work demonstrates the favorable properties of cocrystals and strategies that facilitate their meaningful characterization.

Parents and the media: causes and consequences of parental media socialization

NARCIS (Netherlands)

Notten, N.J.W.R.

2011-01-01

Media literacy is an important part of socialization and with media use becoming ever more essential in modern society, research on parental media socialization is vital. This study proposes the intergenerational transmission of parent’s media competencies, as a specific kind of cultural

Radiation-induced nitration of organic compounds in aqueous solutions

International Nuclear Information System (INIS)

Ershov, B.G.; Gordeev, A.V.; Bykov, G.L.; Moisy, P.

2012-01-01

Radiolysis in aqueous nitrate and acetic acid solutions and nitrate/nitric acid and phenol was studied. The radiolysis of these solutes occurs with circle NO 2 radical, which is the active nitrating agent. Accumulation of nitromethane and nitrite was determined during γ-irradiation of aqueous solutions containing acetic and nitrate solutions. Irradiation of aqueous phenol-nitrate/nitric acid solutions results in the formation of 2- and 4-nitrophenols.

Radiation-induced nitration of organic compounds in aqueous solutions

Energy Technology Data Exchange (ETDEWEB)

Ershov, B.G.; Gordeev, A.V.; Bykov, G.L. [Russian Academy of Sciences, Moscow (Russian Federation). Frumkin Inst. of Physical Chemistry and Electrochemistry; Moisy, P. [CEA, Bagnols sur Ceze (France). Nuclear Energy Div.

2012-07-01

Radiolysis in aqueous nitrate and acetic acid solutions and nitrate/nitric acid and phenol was studied. The radiolysis of these solutes occurs with {sup circle} NO{sup 2} radical, which is the active nitrating agent. Accumulation of nitromethane and nitrite was determined during {gamma}-irradiation of aqueous solutions containing acetic and nitrate solutions. Irradiation of aqueous phenol-nitrate/nitric acid solutions results in the formation of 2- and 4-nitrophenols.

Experimental research on intraocular aqueous flow by PIV method.

Science.gov (United States)

Yang, Hongyu; Song, Hongfang; Mei, Xi; Li, Lin; Fu, Xineng; Zhang, Mindi; Liu, Zhicheng

2013-10-21

Aqueous humor flows regularly from posterior chamber to anterior chamber, and this flow much involves intraocular pressure, the eye tissue nutrition and metabolism. To visualize and measure the intraocular flow regular pattern of aqueous humor. Intraocular flow in the vitro eyeball is driven to simulate the physiological aqueous humor flow, and the flow field is measured by Particle Image Velocimetry(PIV). Fluorescent particle solution of a certain concentration was infused into the root of Posterior Chamber(PC) of vitro rabbit eye to simulate the generation of aqueous and was drained out at a certain hydrostatic pressure from the angle of Anterior Chamber(AC) to represent the drainage of aqueous. PIV method was used to record and calculate the flow on the midsagittal plane of the eyeball. Velocity vector distribution in AC has been obtained, and the distribution shows symmetry feature to some extent. Fluorescent particle solution first fills the PC as it is continuously infused, then surges into AC through the pupil, flows upwards toward the central cornea, reflecting and scattering, and eventually converges along the inner cornea surface towards the outflow points at the periphery of the eyeball. Velocity values around the pupillary margin are within the range of 0.008-0.012 m/s, which are close to theoretical values of 0.0133 m/s, under the driving rate of 100 μl/min. Flow field of aqueous humor can be measured by PIV method, which makes it possible to study the aqueous humor dynamics by experimental method. Our study provides a basis for experimental research on aqueous humor flow; further, it possibly helps to diagnose and treat eye diseases as shear force damage of ocular tissues and destructions on corneal endothelial cells from the point of intraocular flow field.

Thermodynamic properties of potassium chloride aqueous solutions

Science.gov (United States)

Zezin, Denis; Driesner, Thomas

2017-04-01

Potassium chloride is a ubiquitous salt in natural fluids, being the second most abundant dissolved salt in many geological aqueous solutions after sodium chloride. It is a simple solute and strong electrolyte easily dissociating in water, however the thermodynamic properties of KCl aqueous solutions were never correlated with sufficient accuracy for a wide range of physicochemical conditions. In this communication we propose a set of parameters for a Pitzer-type model which allows calculation of all necessary thermodynamic properties of KCl solution, namely excess Gibbs free energy and derived activity coefficient, apparent molar enthalpy, heat capacity and volume, as well as osmotic coefficient and activity of water in solutions. The system KCl-water is one of the best studied aqueous systems containing electrolytes. Although extensive experimental data were collected for thermodynamic properties of these solutions over the years, the accurate volumetric data became available only recently, thus making possible a complete thermodynamic formulation including a pressure dependence of excess Gibbs free energy and derived properties of the KCl-water liquids. Our proposed model is intended for calculation of major thermodynamic properties of KCl aqueous solutions at temperatures ranging from freezing point of a solution to 623 K, pressures ranging from saturated water vapor up to 150 MPa, and concentrations up to the salt saturation. This parameterized model will be further implemented in geochemical software packages and can facilitate the calculation of aqueous equilibrium for reactive transport codes.

Media Literacy Bibliography.

Science.gov (United States)

Duncan, Barry

1989-01-01

Provides an up-to-date bibliography of resources available for teaching media literacy. Groups resources into the areas of media education methodology, mass media texts, general background, television, film, the news and medium of print, advertising, gender and the media, popular culture, popular music and rock video, periodicals, and…

Plasmon-driven sequential chemical reactions in an aqueous environment.

Science.gov (United States)

Zhang, Xin; Wang, Peijie; Zhang, Zhenglong; Fang, Yurui; Sun, Mengtao

2014-06-24

Plasmon-driven sequential chemical reactions were successfully realized in an aqueous environment. In an electrochemical environment, sequential chemical reactions were driven by an applied potential and laser irradiation. Furthermore, the rate of the chemical reaction was controlled via pH, which provides indirect evidence that the hot electrons generated from plasmon decay play an important role in plasmon-driven chemical reactions. In acidic conditions, the hot electrons were captured by the abundant H(+) in the aqueous environment, which prevented the chemical reaction. The developed plasmon-driven chemical reactions in an aqueous environment will significantly expand the applications of plasmon chemistry and may provide a promising avenue for green chemistry using plasmon catalysis in aqueous environments under irradiation by sunlight.

Parenting and Digital Media.

Science.gov (United States)

Coyne, Sarah M; Radesky, Jenny; Collier, Kevin M; Gentile, Douglas A; Linder, Jennifer Ruh; Nathanson, Amy I; Rasmussen, Eric E; Reich, Stephanie M; Rogers, Jean

2017-11-01

Understanding the family dynamic surrounding media use is crucial to our understanding of media effects, policy development, and the targeting of individuals and families for interventions to benefit child health and development. The Families, Parenting, and Media Workgroup reviewed the relevant research from the past few decades. We find that child characteristics, the parent-child relationship, parental mediation practices, and parents' own use of media all can influence children's media use, their attitudes regarding media, and the effects of media on children. However, gaps remain. First, more research is needed on best practices of parental mediation for both traditional and new media. Ideally, this research will involve large-scale, longitudinal studies that manage children from infancy to adulthood. Second, we need to better understand the relationship between parent media use and child media use and specifically how media may interfere with or strengthen parent-child relationships. Finally, longitudinal research on how developmental processes and individual child characteristics influence the intersection between media and family life is needed. The majority of children's media use takes place within a wider family dynamic. An understanding of this dynamic is crucial to understanding child media use as a whole. Copyright © 2017 by the American Academy of Pediatrics.

Social Media, Traditional Media and Marketing Communication of Public Relations

DEFF Research Database (Denmark)

Khajeheian, Datis; Mirahmadi, Fereshteh